# RGD-PIPELINE: ftp-file-extracts # MODULE: annotations-version-1.1.9 (Oct 10, 2019) # GENERATED-ON: 2024/11/16 # PURPOSE: annotations about active Mouse objects extracted from RGD database # ONTOLOGY: MP: Mammalian Phenotype # CONTACT: rgd.data@mcw.edu # FORMAT: tab delimited text # NOTES: multiple values in a single column are separated by '|' # #COLUMN INFORMATION: # #1 RGD_ID unique RGD_ID of the annotated object #2 OBJECT_SYMBOL official symbol of the annotated object #3 OBJECT_NAME official name of the annotated object #4 OBJECT_TYPE annotated object data type: one of ['gene','qtl','strain'] #5 TERM_ACC_ID ontology term accession id #6 TERM_NAME ontology term name #7 QUALIFIER optional qualifier #8 EVIDENCE evidence #9 WITH with info #10 ASPECT aspect #11 REFERENCES db references (Reference RGDID|PUBMED ID) #12 CREATED_DATE created date #13 ASSIGNED_BY assigned by #14 MESH_OMIM_ID MESH:xxx or OMIM:xxx id corresponding to RDO:xxx id found in TERM_ACC_ID column (RGD/CTD Disease Ontology annotations only) #15 CURATION_NOTES curation notes provided by RGD curators #16 ORIGINAL_REFERENCE original reference RGD_ID OBJECT_SYMBOL OBJECT_NAME OBJECT_TYPE TERM_ACC_ID TERM_NAME QUALIFIER EVIDENCE WITH ASPECT REFERENCES CREATED_DATE ASSIGNED_BY MESH_OMIM_ID CURATION_NOTES ORIGINAL_REFERENCE 10010253 Chaer1 cardiac hypertrophy associated epigenetic regulator 1 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20170817 MGI PMID:27618650 10011098 Gm40600 predicted gene, 40600 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0008896 increased IgG2c level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011098 Gm40600 predicted gene, 40600 gene MP:0013940 abnormal plasmablast number IAGP N RGD:5509061 20211125 MGI PMID:33987830 10011153 Discn DNA damage-induced stem cell specific noncoding RNA gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20231102 MGI PMID:34552092 10011153 Discn DNA damage-induced stem cell specific noncoding RNA gene MP:0001405 impaired coordination IAGP N RGD:5509061 20231102 MGI PMID:34552092 10011153 Discn DNA damage-induced stem cell specific noncoding RNA gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20231102 MGI PMID:34552092 10011153 Discn DNA damage-induced stem cell specific noncoding RNA gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20231102 MGI PMID:34552092 10011153 Discn DNA damage-induced stem cell specific noncoding RNA gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20231102 MGI PMID:34552092 10011153 Discn DNA damage-induced stem cell specific noncoding RNA gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20231102 MGI PMID:34552092 10011153 Discn DNA damage-induced stem cell specific noncoding RNA gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20231102 MGI PMID:34552092 10021856 Percc1 proline and glutamate rich with coiled coil 1 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20200123 MGI PMID:31217582 10021856 Percc1 proline and glutamate rich with coiled coil 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200123 MGI PMID:31217582 10021856 Percc1 proline and glutamate rich with coiled coil 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200123 MGI PMID:31217582 10021856 Percc1 proline and glutamate rich with coiled coil 1 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20200123 MGI PMID:31217582 10021856 Percc1 proline and glutamate rich with coiled coil 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200123 MGI PMID:31217582 10021856 Percc1 proline and glutamate rich with coiled coil 1 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20200123 MGI PMID:31217582 10036919 Gm41610 predicted gene, 41610 gene MP:0008608 increased circulating interleukin-13 level IAGP N RGD:5509061 20210506 MGI PMID:33568531 10036919 Gm41610 predicted gene, 41610 gene MP:0008626 increased circulating interleukin-5 level IAGP N RGD:5509061 20210506 MGI PMID:33568531 10036919 Gm41610 predicted gene, 41610 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20210506 MGI PMID:33568531 10036919 Gm41610 predicted gene, 41610 gene MP:0012358 decreased partial thromboplastin time IAGP N RGD:5509061 20210506 MGI PMID:33568531 10043078 Gm13030 predicted gene 13030 gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20210610 MGI PMID:31436535 10043844 Hdlq92_m HDL QTL 92 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:18772481 10043844 Hdlq92_m HDL QTL 92 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:18772481 10043846 Hdlq91_m HDL QTL 91 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:18048852 10043846 Hdlq91_m HDL QTL 91 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:18048852 10043847 Hdlq89_m HDL QTL 89 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:14872007 10043847 Hdlq89_m HDL QTL 89 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:14872007 10043848 Hdlq90_m HDL QTL 90 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:14872007 10043848 Hdlq90_m HDL QTL 90 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:14872007 10043850 Trigq3_m triglyceride QTL 3 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20150604 MGI PMID:18048852 10043850 Trigq3_m triglyceride QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:18048852 10043852 Hdlq86_m HDL QTL 86 (mouse) qtl MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:18048852 10043852 Hdlq86_m HDL QTL 86 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:18048852 10043852 Hdlq86_m HDL QTL 86 (mouse) qtl MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:18048852 10043852 Hdlq86_m HDL QTL 86 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20150604 MGI PMID:18048852 10043852 Hdlq86_m HDL QTL 86 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:18048852 10043855 Hdlq83_m HDL QTL 83 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:16685081 10043855 Hdlq83_m HDL QTL 83 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:16685081 10043857 Cia39_m collagen induced arthritis 39 (mouse) qtl MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20150604 MGI PMID:15761851 10043857 Cia39_m collagen induced arthritis 39 (mouse) qtl MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20150604 MGI PMID:15761851 10043857 Cia39_m collagen induced arthritis 39 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:15761851 10043857 Cia39_m collagen induced arthritis 39 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:15761851 10043878 Adip20_m adiposity 20 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20150604 MGI PMID:12856282 10043878 Adip20_m adiposity 20 (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20150604 MGI PMID:17103052 10043878 Adip20_m adiposity 20 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20150604 MGI PMID:17103052 10043878 Adip20_m adiposity 20 (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20150604 MGI PMID:17103052 10043878 Adip20_m adiposity 20 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:12856282 10043878 Adip20_m adiposity 20 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:12856282 10043878 Adip20_m adiposity 20 (mouse) qtl MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20150604 MGI PMID:17103052 10043878 Adip20_m adiposity 20 (mouse) qtl MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20150604 MGI PMID:17103052 10043884 Bhr8_m bronchial hyperresponsiveness 8 (mouse) qtl MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20150604 MGI PMID:15657107 10043884 Bhr8_m bronchial hyperresponsiveness 8 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:15657107 10043890 Trigq4_m triglyceride QTL 4 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20150611 MGI PMID:18048852 10043890 Trigq4_m triglyceride QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:18048852 10043899 Hdlq99_m HDL QTL 99 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:14872007 10043899 Hdlq99_m HDL QTL 99 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:14872007 10043900 Hdlq102_m HDL QTL 102 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:18772481 10043900 Hdlq102_m HDL QTL 102 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:18772481 10043915 Obq36_m obesity QTL 36 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20150604 MGI PMID:11210195 10043915 Obq36_m obesity QTL 36 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:11210195 10043920 Afpq11_m abdominal fat percent QTL 11 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20150604 MGI PMID:11116089 10043920 Afpq11_m abdominal fat percent QTL 11 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:11116089 10043922 Alcw9_m alcohol withdrawal 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:16436183 10043922 Alcw9_m alcohol withdrawal 9 (mouse) qtl MP:0005443 abnormal ethanol metabolism IAGP N RGD:5509061 20150604 MGI PMID:16436183 10043958 Chldq12_m cholesterol and HDL QTL 12 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:17496333 10043958 Chldq12_m cholesterol and HDL QTL 12 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:17496333 10043958 Chldq12_m cholesterol and HDL QTL 12 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:17496333 10043966 Pnhdlc6_m plasma non-HDK cholesterol 6 (mouse) qtl MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:18048852 10043966 Pnhdlc6_m plasma non-HDK cholesterol 6 (mouse) qtl MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:18048852 10043966 Pnhdlc6_m plasma non-HDK cholesterol 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:18048852 10043979 Hdlq67_m HDL QTL 67 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:14701919 10043979 Hdlq67_m HDL QTL 67 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:14701919 10043985 Stheal12_m soft tissue heal 12 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:16341671 10043991 Bw36_m body weight QTL 36 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20150604 MGI PMID:11116089 10043991 Bw36_m body weight QTL 36 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:11116089 10043994 Bw37_m body weight QTL 37 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20150604 MGI PMID:11116089 10043994 Bw37_m body weight QTL 37 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:11116089 10043996 Gct5_m granulosa cell tumorigenesis 5 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:15735010 10043996 Gct5_m granulosa cell tumorigenesis 5 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15735010 10043996 Gct5_m granulosa cell tumorigenesis 5 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15735010 10043996 Gct5_m granulosa cell tumorigenesis 5 (mouse) qtl MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20150604 MGI PMID:15735010 10044002 Hdl7_m HDL level 7 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:12588951 10044002 Hdl7_m HDL level 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:12588951 10044003 Hdlq13_m HDL QTL 13 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20150604 MGI PMID:14701919 10044003 Hdlq13_m HDL QTL 13 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:14701919 10044004 Stzid3_m streptozotocin induced diabetes susceptibility 3 (mouse) qtl MP:0001263 weight loss IAGP N RGD:5509061 20150604 MGI PMID:15670764 10044004 Stzid3_m streptozotocin induced diabetes susceptibility 3 (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20150604 MGI PMID:15670764 10044004 Stzid3_m streptozotocin induced diabetes susceptibility 3 (mouse) qtl MP:0001759 increased urine glucose level IAGP N RGD:5509061 20150604 MGI PMID:15670764 10044004 Stzid3_m streptozotocin induced diabetes susceptibility 3 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:15670764 10044004 Stzid3_m streptozotocin induced diabetes susceptibility 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:15670764 10044004 Stzid3_m streptozotocin induced diabetes susceptibility 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:15670764 10044009 Tglq4_m triglyceride QTL 4 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20150604 MGI PMID:17496333 10044009 Tglq4_m triglyceride QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:17496333 10044010 Alcp26_m alcohol preference locus 26, male specific (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20150604 MGI PMID:10443995 10044010 Alcp26_m alcohol preference locus 26, male specific (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:10443995 10044196 Teyorf1 testis expressed, Chromosome Y open reading frame 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20230330 MGI PMID:35485405 10044207 Prssly serine protease-like, Chr Y gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20230330 MGI PMID:35485405 10045613 Rapop7_m radiation-induced apoptosis 6 (mouse) qtl MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20150618 MGI PMID:9367689 10045613 Rapop7_m radiation-induced apoptosis 6 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:9367689 10045618 Heal17_m wound healing/regeneration 17 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20150618 MGI PMID:9751744 10045618 Heal17_m wound healing/regeneration 17 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:12682777 10045619 Heal14_m wound healing/regeneration 14 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20150618 MGI PMID:12682777 10045619 Heal14_m wound healing/regeneration 14 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:12682777 10045621 Heal21_m wound healing/regeneration 21 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20150618 MGI PMID:9751744 10045621 Heal21_m wound healing/regeneration 21 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:12682777 10045623 Heal18_m wound healing regeneration 18 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20150618 MGI PMID:9751744 10045623 Heal18_m wound healing regeneration 18 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:12682777 10045626 Tir4_m trypanosome infection response 4 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20150618 MGI PMID:15859356 10045626 Tir4_m trypanosome infection response 4 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20150618 MGI PMID:18253157 10045626 Tir4_m trypanosome infection response 4 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20150618 MGI PMID:9171834 10045626 Tir4_m trypanosome infection response 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:9171834 10045644 Skts16_m skin tumor susceptibility 16 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:11309660 10045644 Skts16_m skin tumor susceptibility 16 (mouse) qtl MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20150618 MGI PMID:11309660 10045644 Skts16_m skin tumor susceptibility 16 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20150618 MGI PMID:11309660 10045644 Skts16_m skin tumor susceptibility 16 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:11309660 10045886 Cplaq14_m circadian period of locomotor activity 14 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20150619 MGI Created by mouse qtl pipeline PMID:14667146 10045886 Cplaq14_m circadian period of locomotor activity 14 (mouse) qtl MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:14667146 10045887 Cplaq13_m circadian period of locomotor activity 13 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20150619 MGI Created by mouse qtl pipeline PMID:10547923 10045887 Cplaq13_m circadian period of locomotor activity 13 (mouse) qtl MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:10547923 10045977 Tir9_m trypanosome infection response 9 (mouse) qtl MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20150702 MGI PMID:12847546 10045977 Tir9_m trypanosome infection response 9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150626 MGI Created by mouse qtl pipeline PMID:12847546 10045978 Tir10_m trypanosome infection response 10 (mouse) qtl MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20150702 MGI PMID:12847546 10045978 Tir10_m trypanosome infection response 10 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150626 MGI Created by mouse qtl pipeline PMID:12847546 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20220519 MGI 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20151126 MGI PMID:25168382 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20220811 MGI 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20151126 MGI PMID:25168382 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20220811 MGI 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20220811 MGI 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20151126 MGI PMID:25168382 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220519 MGI 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 10051 Abcd3 ATP-binding cassette, sub-family D member 3 gene MP:0014010 abnormal peroxisome morphology IAGP N RGD:5509061 20230615 MGI PMID:25168382 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0002763 ectopic Bergmann glia cells IAGP N RGD:5509061 20141003 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:9825957 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0005357 novel environmental response-related retropulsion IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0006098 absent cerebellar lobules IAGP N RGD:5509061 20141003 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0009216 abnormal peritoneum morphology IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20141003 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0009268 absent cerebellum fissure IAGP N RGD:5509061 20141003 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15987940 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0009978 abnormal cerebellum white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:9883720 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0013551 decreased cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20161201 MGI PMID:20980600 10053 Abl2 ABL proto-oncogene 2, non-receptor tyrosine kinase gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20190704 MGI PMID:9883720 10053675 Eae44b_m experimental allergic encephalomyelitis susceptibility 44b (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150717 MGI Created by mouse qtl pipeline PMID:9712054 10053676 Eae44a_m experimental allergic encephalomyelitis susceptibility 44a (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20150717 MGI Created by mouse qtl pipeline PMID:9712054 10053676 Eae44a_m experimental allergic encephalomyelitis susceptibility 44a (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150717 MGI Created by mouse qtl pipeline PMID:9712054 10053677 Eae46_m experimental allergic encephalomyelitis susceptibility 46 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20150717 MGI Created by mouse qtl pipeline PMID:12517969 10053677 Eae46_m experimental allergic encephalomyelitis susceptibility 46 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150717 MGI Created by mouse qtl pipeline PMID:12517969 10053680 Lith25_m lithogenic gene 25 (mouse) qtl MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20150723 MGI PMID:12837957 10053680 Lith25_m lithogenic gene 25 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20150723 MGI PMID:12810825 10053680 Lith25_m lithogenic gene 25 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20150717 MGI Created by mouse qtl pipeline PMID:12837957 10053680 Lith25_m lithogenic gene 25 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150717 MGI Created by mouse qtl pipeline PMID:12837957 10053681 Lith24_m lithogenic gene 24 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20150723 MGI PMID:12810825 10053681 Lith24_m lithogenic gene 24 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20150717 MGI Created by mouse qtl pipeline PMID:12810825 10053685 Eae43_m experimental allergic encephalomyelitis susceptibility 43 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20150723 MGI PMID:10072563 10053685 Eae43_m experimental allergic encephalomyelitis susceptibility 43 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20150723 MGI PMID:9712054 10053685 Eae43_m experimental allergic encephalomyelitis susceptibility 43 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150717 MGI Created by mouse qtl pipeline PMID:10072563 10053686 Eae42_m experimental allergic encephalomyelitis susceptibility 42 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20150723 MGI PMID:8757345 10053686 Eae42_m experimental allergic encephalomyelitis susceptibility 42 (mouse) qtl MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20150723 MGI PMID:8757345 10053686 Eae42_m experimental allergic encephalomyelitis susceptibility 42 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150717 MGI Created by mouse qtl pipeline PMID:8757345 10054061 Lith28_m lithogenic gene 28 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20150730 MGI PMID:16151694 10054061 Lith28_m lithogenic gene 28 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20150724 MGI Created by mouse qtl pipeline PMID:16151694 10054062 Lith29_m lithogenic gene 29 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20150730 MGI PMID:16151694 10054062 Lith29_m lithogenic gene 29 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20150724 MGI Created by mouse qtl pipeline PMID:16151694 10054269 Nba11_m New Zealand Black autoimmunity 11 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20150806 MGI PMID:12215897 10054269 Nba11_m New Zealand Black autoimmunity 11 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20150731 MGI Created by mouse qtl pipeline PMID:12215897 10054269 Nba11_m New Zealand Black autoimmunity 11 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150731 MGI Created by mouse qtl pipeline PMID:12215897 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20150806 MGI PMID:16493085 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20150806 MGI PMID:18606711 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0002493 increased IgG level IAGP N RGD:5509061 20150806 MGI PMID:15986357 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0002494 increased IgM level IAGP N RGD:5509061 20150806 MGI PMID:15986357 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20150806 MGI PMID:18606711 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20150806 MGI PMID:15634937 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20150806 MGI PMID:15986357 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20150806 MGI PMID:18606711 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20150806 MGI PMID:18606711 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20150806 MGI PMID:15634937 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20150806 MGI PMID:15986357 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20150806 MGI PMID:15634937 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20150806 MGI PMID:15986357 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20150806 MGI PMID:15634937 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20150806 MGI PMID:15986357 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20150806 MGI PMID:18606711 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0005014 increased B cell number IAGP N RGD:5509061 20150806 MGI PMID:15986357 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20150806 MGI PMID:15634937 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20150731 MGI Created by mouse qtl pipeline PMID:15634937 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150731 MGI Created by mouse qtl pipeline PMID:15634937 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20150731 MGI Created by mouse qtl pipeline PMID:15634937 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0005615 increased susceptibility to type III hypersensitivity reaction IAGP N RGD:5509061 20150806 MGI PMID:15634937 10054270 Nba10_m New Zealand Black autoimmunity 10 (mouse) qtl MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20150806 MGI PMID:15986357 10054272 Nba8_m New Zealand Black autoimmunity 8 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20150806 MGI PMID:11739537 10054272 Nba8_m New Zealand Black autoimmunity 8 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20150731 MGI Created by mouse qtl pipeline PMID:11739537 10054272 Nba8_m New Zealand Black autoimmunity 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150731 MGI Created by mouse qtl pipeline PMID:11739537 10054475 Ossc3_m osteosarcoma susceptibility 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20150807 MGI Created by mouse qtl pipeline PMID:16331598 10054475 Ossc3_m osteosarcoma susceptibility 3 (mouse) qtl MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20150813 MGI PMID:16331598 10054475 Ossc3_m osteosarcoma susceptibility 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16331598 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:9861014 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11590124 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:9861014 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:9861014 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11590124 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9861014 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11590124 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9861014 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11590124 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:9861014 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9861014 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20141003 MGI PMID:11590124 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:9861014 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:11590124 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0005283 increased unsaturated fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:9861014 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11590124 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:9861014 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0008570 lipidosis IAGP N RGD:5509061 20141003 MGI PMID:9861014 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0011019 abnormal adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:9802886 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9861014 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0030613 dicarboxylic aciduria IAGP N RGD:5509061 20180906 MGI PMID:11590124 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0030613 dicarboxylic aciduria IAGP N RGD:5509061 20180906 MGI PMID:9861014 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:11590124 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:9861014 10056 Acadl acyl-Coenzyme A dehydrogenase, long-chain gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:9861014 10057 Acadm acyl-Coenzyme A dehydrogenase, medium chain gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16121256 10057 Acadm acyl-Coenzyme A dehydrogenase, medium chain gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20210128 MGI 10057 Acadm acyl-Coenzyme A dehydrogenase, medium chain gene MP:0002764 short tibia IEA N RGD:5509061 20230601 MGI 10057 Acadm acyl-Coenzyme A dehydrogenase, medium chain gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16121256 10057 Acadm acyl-Coenzyme A dehydrogenase, medium chain gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20141003 MGI PMID:16121256 10057 Acadm acyl-Coenzyme A dehydrogenase, medium chain gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:16121256 10057 Acadm acyl-Coenzyme A dehydrogenase, medium chain gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:16121256 10057 Acadm acyl-Coenzyme A dehydrogenase, medium chain gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16121256 10057 Acadm acyl-Coenzyme A dehydrogenase, medium chain gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16121256 10057 Acadm acyl-Coenzyme A dehydrogenase, medium chain gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16121256 10057 Acadm acyl-Coenzyme A dehydrogenase, medium chain gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 10057 Acadm acyl-Coenzyme A dehydrogenase, medium chain gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:16121256 10057 Acadm acyl-Coenzyme A dehydrogenase, medium chain gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16121256 10057 Acadm acyl-Coenzyme A dehydrogenase, medium chain gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:16121256 10057 Acadm acyl-Coenzyme A dehydrogenase, medium chain gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:16121256 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15025677 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:16199475 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11590124 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:24285112 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12893739 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16199475 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:24285112 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15025677 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:24285112 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:12893739 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15025677 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11590124 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15025677 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11590124 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:11590124 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:24285112 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:24285112 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:24285112 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0002899 fatigue IAGP N RGD:5509061 20141003 MGI PMID:15025677 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16199475 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12893739 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:24285112 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20141003 MGI PMID:11590124 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:12893739 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:24285112 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15025677 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:12893739 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:15025677 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:16199475 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16199475 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:24285112 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0005439 decreased glycogen level IAGP N RGD:5509061 20141003 MGI PMID:16199475 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:24285112 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11590124 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15025677 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16199475 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:24285112 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:24285112 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:16199475 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:24285112 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0011019 abnormal adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:24285112 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:15025677 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:16199475 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20240229 MGI PMID:16199475 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20230119 MGI 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:16199475 10058 Acadvl acyl-Coenzyme A dehydrogenase, very long chain gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:24285112 10060 Acat1 acetyl-Coenzyme A acetyltransferase 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20240523 MGI 10061 Asic2 acid-sensing ion channel 2 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:18296560 10061 Asic2 acid-sensing ion channel 2 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 10061 Asic2 acid-sensing ion channel 2 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:14762118 10061 Asic2 acid-sensing ion channel 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 10061 Asic2 acid-sensing ion channel 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11069180 10061 Asic2 acid-sensing ion channel 2 gene MP:0002989 small kidney IEA N RGD:5509061 20201022 MGI 10061 Asic2 acid-sensing ion channel 2 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:18296560 10061 Asic2 acid-sensing ion channel 2 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:17531389 10061 Asic2 acid-sensing ion channel 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:14762118 10061 Asic2 acid-sensing ion channel 2 gene MP:0006335 abnormal hearing electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15537887 10061 Asic2 acid-sensing ion channel 2 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 10064 Acly ATP citrate lyase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20141003 MGI 10064 Acly ATP citrate lyase gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14662765 10066 Aco1 aconitase 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 10066 Aco1 aconitase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15208438 10066 Aco1 aconitase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16283625 10066 Aco1 aconitase 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 10066 Aco1 aconitase 1 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14726953 10066 Aco1 aconitase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23135277 10066 Aco1 aconitase 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15208438 10066 Aco1 aconitase 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16283625 10068 Acp1 acid phosphatase 1, soluble gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161013 MGI PMID:26213100 10068 Acp1 acid phosphatase 1, soluble gene MP:0001265 decreased body size IEA N RGD:5509061 20141003 MGI 10068 Acp1 acid phosphatase 1, soluble gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20161013 MGI PMID:26213100 10068 Acp1 acid phosphatase 1, soluble gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20161013 MGI PMID:26213100 10068 Acp1 acid phosphatase 1, soluble gene MP:0008705 increased interleukin-6 secretion IEA N RGD:5509061 20141003 MGI 10068 Acp1 acid phosphatase 1, soluble gene MP:0011703 increased fibroblast proliferation IEA N RGD:5509061 20141003 MGI 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:9228031 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9228031 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:9228031 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:9228031 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:9228031 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000888 absent cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20160804 MGI 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160623 MGI 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:9228031 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20141003 MGI 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9228031 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:9228031 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0004604 abnormal vertebral pedicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9228031 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:9228031 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0004924 abnormal behavior IEA N RGD:5509061 20141003 MGI 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0005014 increased B cell number IEA N RGD:5509061 20160804 MGI 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0005018 decreased T cell number IEA N RGD:5509061 20141003 MGI 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:9228031 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0005060 accumulation of giant lysosomes in kidney/renal tubule cells IAGP N RGD:5509061 20141003 MGI PMID:9228031 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20141003 MGI 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20141003 MGI 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0009351 thin hair shaft IAGP N RGD:5509061 20141003 MGI PMID:15503243 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0010932 increased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:9228031 10070 Acp2 acid phosphatase 2, lysosomal gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:9228031 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0000132 thickened long bone epiphysis IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0006394 abnormal vertebral epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:8898228 10072 Acp5 acid phosphatase 5, tartrate resistant gene MP:0030791 club-shaped femur IAGP N RGD:5509061 20181011 MGI PMID:8898228 10076 Acr acrosin prepropeptide gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:15685642 10076 Acr acrosin prepropeptide gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15685642 10076 Acr acrosin prepropeptide gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15685642 10076 Acr acrosin prepropeptide gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12930723 10076 Acr acrosin prepropeptide gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15685642 10076 Acr acrosin prepropeptide gene MP:0005411 delayed fertilization IAGP N RGD:5509061 20141003 MGI PMID:7989357 10076 Acr acrosin prepropeptide gene MP:0005411 delayed fertilization IAGP N RGD:5509061 20141003 MGI PMID:9041140 10076 Acr acrosin prepropeptide gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:15685642 10076 Acr acrosin prepropeptide gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191017 MGI PMID:15685642 10076 Acr acrosin prepropeptide gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20200227 MGI PMID:15685642 10077 Actg2 actin, gamma 2, smooth muscle, enteric gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20240229 MGI PMID:36264152 10077 Actg2 actin, gamma 2, smooth muscle, enteric gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20240229 MGI PMID:36264152 10077 Actg2 actin, gamma 2, smooth muscle, enteric gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20240229 MGI PMID:36264152 10077 Actg2 actin, gamma 2, smooth muscle, enteric gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 10077 Actg2 actin, gamma 2, smooth muscle, enteric gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20240523 MGI 10077 Actg2 actin, gamma 2, smooth muscle, enteric gene MP:0003620 oliguria IAGP N RGD:5509061 20240229 MGI PMID:36264152 10077 Actg2 actin, gamma 2, smooth muscle, enteric gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 10077 Actg2 actin, gamma 2, smooth muscle, enteric gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20240229 MGI PMID:36264152 10077 Actg2 actin, gamma 2, smooth muscle, enteric gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20240229 MGI PMID:36264152 10077 Actg2 actin, gamma 2, smooth muscle, enteric gene MP:0011923 abnormal bladder urine volume IAGP N RGD:5509061 20240229 MGI PMID:36264152 10078 Acvr2b activin receptor IIB gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:16991118 10078 Acvr2b activin receptor IIB gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0000650 mesocardia IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:10452853 10078 Acvr2b activin receptor IIB gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10452853 10078 Acvr2b activin receptor IIB gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:10452853 10078 Acvr2b activin receptor IIB gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:10452853 10078 Acvr2b activin receptor IIB gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16991118 10078 Acvr2b activin receptor IIB gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10452853 10078 Acvr2b activin receptor IIB gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16991118 10078 Acvr2b activin receptor IIB gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16991118 10078 Acvr2b activin receptor IIB gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 10078 Acvr2b activin receptor IIB gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16991118 10078 Acvr2b activin receptor IIB gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 10078 Acvr2b activin receptor IIB gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:10452853 10078 Acvr2b activin receptor IIB gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:16991118 10078 Acvr2b activin receptor IIB gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:15542835 10078 Acvr2b activin receptor IIB gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16991118 10078 Acvr2b activin receptor IIB gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:15542835 10078 Acvr2b activin receptor IIB gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0004651 increased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:10452853 10078 Acvr2b activin receptor IIB gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10452853 10078 Acvr2b activin receptor IIB gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0006206 embryonic lethality between somite formation and embryo turning IAGP N RGD:5509061 20141003 MGI PMID:16991118 10078 Acvr2b activin receptor IIB gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210520 MGI 10078 Acvr2b activin receptor IIB gene MP:0010238 increased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:22869749 10078 Acvr2b activin receptor IIB gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9242489 10078 Acvr2b activin receptor IIB gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10452853 10078 Acvr2b activin receptor IIB gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10452853 10078 Acvr2b activin receptor IIB gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 10078 Acvr2b activin receptor IIB gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 10078 Acvr2b activin receptor IIB gene MP:0011191 increased embryonic epiblast cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10452853 10078 Acvr2b activin receptor IIB gene MP:0012081 absent heart tube IAGP N RGD:5509061 20141003 MGI PMID:10452853 10078 Acvr2b activin receptor IIB gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:10452853 10078 Acvr2b activin receptor IIB gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:16991118 10078 Acvr2b activin receptor IIB gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:10452853 10078 Acvr2b activin receptor IIB gene MP:0012724 absent head fold IAGP N RGD:5509061 20141003 MGI PMID:10452853 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000231 hypertension IAGP N RGD:5509061 20151224 MGI PMID:26398936 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:12970115 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10716993 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11062473 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000262 poor arterial differentiation IAGP N RGD:5509061 20141003 MGI PMID:22783020 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:22783020 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:22783020 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:22783020 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:10716993 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:12941632 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:10716993 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12588795 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:12588795 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:12588795 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20151224 MGI PMID:26398936 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10716993 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:22783020 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:17911384 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11062473 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12588795 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17911384 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12588795 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11062473 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12941632 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0002138 abnormal hepatobiliary system morphology IAGP N RGD:5509061 20141003 MGI PMID:12588795 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11062473 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12941632 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17911384 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12941632 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0002976 vascular smooth muscle hypotrophy IAGP N RGD:5509061 20141003 MGI PMID:17911384 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10716993 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11062473 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17911384 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22783020 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0003292 melena IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:10716993 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10716993 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17911384 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22783020 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17911384 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:22783020 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:10716993 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:12941632 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:11062473 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:22783020 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004175 telangiectasia IAGP N RGD:5509061 20141003 MGI PMID:12588795 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20151224 MGI PMID:26398936 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:12941632 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:12941632 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12941632 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:17911384 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:22783020 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20160623 MGI PMID:25082229 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:10716993 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:17911384 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:22783020 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10716993 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20151224 MGI PMID:26398936 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:12941632 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10716993 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:11062473 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0005662 increased circulating adrenaline level IAGP N RGD:5509061 20151224 MGI PMID:26398936 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0005665 increased circulating noradrenaline level IAGP N RGD:5509061 20151224 MGI PMID:26398936 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20141003 MGI PMID:10716993 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20141003 MGI PMID:11062473 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20141003 MGI PMID:17911384 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20160623 MGI PMID:25082229 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20151224 MGI PMID:26398936 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:22783020 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0010480 pulmonary arteriovenous malformation IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0010530 cerebral arteriovenous malformation IAGP N RGD:5509061 20141003 MGI PMID:22571958 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0010531 gastrointestinal arteriovenous malformation IAGP N RGD:5509061 20141003 MGI PMID:19805914 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0010531 gastrointestinal arteriovenous malformation IAGP N RGD:5509061 20160623 MGI PMID:25082229 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0010545 abnormal heart layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22783020 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0011022 abnormal circadian regulation of systemic arterial blood pressure IAGP N RGD:5509061 20151224 MGI PMID:26398936 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10716993 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11062473 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12970115 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17911384 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22783020 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17911384 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10716993 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0012494 dilated pharyngeal arch artery IAGP N RGD:5509061 20141003 MGI PMID:10716993 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20151224 MGI PMID:26398936 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0013139 moribund IAGP N RGD:5509061 20160623 MGI PMID:25082229 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0031156 large intestine hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:25082229 10079 Acvrl1 activin A receptor, type II-like 1 gene MP:0031231 decreased circulating angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:26398936 10080 Acy1 aminoacylase 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 10080 Acy1 aminoacylase 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20240523 MGI 10080 Acy1 aminoacylase 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 10080 Acy1 aminoacylase 1 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20231207 MGI 10080 Acy1 aminoacylase 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 10080 Acy1 aminoacylase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 10081 Ada adenosine deaminase gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0000231 hypertension IAGP N RGD:5509061 20180719 MGI PMID:25538227 10081 Ada adenosine deaminase gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20180719 MGI PMID:7670465 10081 Ada adenosine deaminase gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20180719 MGI PMID:23855769 10081 Ada adenosine deaminase gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20180719 MGI PMID:7670465 10081 Ada adenosine deaminase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180719 MGI PMID:7731963 10081 Ada adenosine deaminase gene MP:0000601 small liver IAGP N RGD:5509061 20180719 MGI PMID:7731963 10081 Ada adenosine deaminase gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20180719 MGI PMID:7731963 10081 Ada adenosine deaminase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180719 MGI PMID:7731963 10081 Ada adenosine deaminase gene MP:0000692 small spleen IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0000706 small thymus IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0001177 atelectasis IAGP N RGD:5509061 20180719 MGI PMID:7670465 10081 Ada adenosine deaminase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180719 MGI PMID:7731963 10081 Ada adenosine deaminase gene MP:0001379 abnormal penile erection IAGP N RGD:5509061 20180719 MGI PMID:18340377 10081 Ada adenosine deaminase gene MP:0001575 cyanosis IAGP N RGD:5509061 20180719 MGI PMID:7670465 10081 Ada adenosine deaminase gene MP:0001575 cyanosis IAGP N RGD:5509061 20180719 MGI PMID:7731963 10081 Ada adenosine deaminase gene MP:0001577 anemia IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20180719 MGI PMID:7670465 10081 Ada adenosine deaminase gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20180719 MGI PMID:7731963 10081 Ada adenosine deaminase gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20180719 MGI PMID:25538227 10081 Ada adenosine deaminase gene MP:0001861 lung inflammation IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:7592575 10081 Ada adenosine deaminase gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20180719 MGI PMID:7670465 10081 Ada adenosine deaminase gene MP:0002336 abnormal pulmonary gas exchange IAGP N RGD:5509061 20180719 MGI PMID:23855769 10081 Ada adenosine deaminase gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20180719 MGI PMID:18559975 10081 Ada adenosine deaminase gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20180719 MGI PMID:25538227 10081 Ada adenosine deaminase gene MP:0002975 vascular smooth muscle hypertrophy IAGP N RGD:5509061 20180719 MGI PMID:23855769 10081 Ada adenosine deaminase gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20180719 MGI PMID:25538227 10081 Ada adenosine deaminase gene MP:0003415 priapism IAGP N RGD:5509061 20180719 MGI PMID:18340377 10081 Ada adenosine deaminase gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20180719 MGI PMID:23855769 10081 Ada adenosine deaminase gene MP:0003718 maternal effect IAGP N RGD:5509061 20180719 MGI PMID:25538227 10081 Ada adenosine deaminase gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20180719 MGI PMID:7731963 10081 Ada adenosine deaminase gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20180719 MGI PMID:23855769 10081 Ada adenosine deaminase gene MP:0004259 small placenta IAGP N RGD:5509061 20180719 MGI PMID:25538227 10081 Ada adenosine deaminase gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20180719 MGI PMID:25538227 10081 Ada adenosine deaminase gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20180719 MGI PMID:7731963 10081 Ada adenosine deaminase gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20180719 MGI PMID:7731963 10081 Ada adenosine deaminase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20180719 MGI PMID:25538227 10081 Ada adenosine deaminase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20180719 MGI PMID:7670465 10081 Ada adenosine deaminase gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20180719 MGI PMID:7731963 10081 Ada adenosine deaminase gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0005426 tachypnea IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20180719 MGI PMID:7731963 10081 Ada adenosine deaminase gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20180719 MGI PMID:25538227 10081 Ada adenosine deaminase gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20180719 MGI PMID:18559975 10081 Ada adenosine deaminase gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0010758 increased right ventricle systolic pressure IAGP N RGD:5509061 20180719 MGI PMID:23855769 10081 Ada adenosine deaminase gene MP:0010896 decreased lung compliance IAGP N RGD:5509061 20180719 MGI PMID:23855769 10081 Ada adenosine deaminase gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20180719 MGI PMID:23855769 10081 Ada adenosine deaminase gene MP:0010935 increased airway resistance IAGP N RGD:5509061 20180719 MGI PMID:23855769 10081 Ada adenosine deaminase gene MP:0011044 increased lung elastance IAGP N RGD:5509061 20180719 MGI PMID:23855769 10081 Ada adenosine deaminase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:25538227 10081 Ada adenosine deaminase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:7731963 10081 Ada adenosine deaminase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:7670465 10081 Ada adenosine deaminase gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20180719 MGI PMID:7731963 10081 Ada adenosine deaminase gene MP:0030876 abnormal costochondral joint morphology IAGP N RGD:5509061 20181101 MGI PMID:9478961 10081 Ada adenosine deaminase gene MP:0031510 increased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:23855769 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10894545 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10894545 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16382140 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:10894545 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0005113 decreased spinal cord ventral horn cell number IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20826656 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10894545 10082 Adarb1 adenosine deaminase, RNA-specific, B1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10894545 10083 Adcy6 adenylate cyclase 6 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:20466003 10083 Adcy6 adenylate cyclase 6 gene MP:0001762 polyuria IAGP N RGD:5509061 20141225 MGI PMID:24431204 10083 Adcy6 adenylate cyclase 6 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141225 MGI PMID:24431204 10083 Adcy6 adenylate cyclase 6 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 10083 Adcy6 adenylate cyclase 6 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:20466003 10083 Adcy6 adenylate cyclase 6 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:21937603 10083 Adcy6 adenylate cyclase 6 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141225 MGI PMID:24431204 10083 Adcy6 adenylate cyclase 6 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18071070 10083 Adcy6 adenylate cyclase 6 gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:20466003 10083 Adcy6 adenylate cyclase 6 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 10083 Adcy6 adenylate cyclase 6 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:20466003 10083 Adcy6 adenylate cyclase 6 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141225 MGI PMID:24431204 10083 Adcy6 adenylate cyclase 6 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:20466003 10083 Adcy6 adenylate cyclase 6 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141225 MGI PMID:24431204 10083 Adcy6 adenylate cyclase 6 gene MP:0010108 abnormal renal water reabsorption IAGP N RGD:5509061 20141003 MGI PMID:20466003 10083 Adcy6 adenylate cyclase 6 gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:18071070 10083 Adcy6 adenylate cyclase 6 gene MP:0011460 decreased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:20466003 10083 Adcy6 adenylate cyclase 6 gene MP:0011467 decreased urine urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:20466003 10083 Adcy6 adenylate cyclase 6 gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:20466003 10083 Adcy6 adenylate cyclase 6 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:20466003 10083 Adcy6 adenylate cyclase 6 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:18071070 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11579206 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11756684 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:11579206 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11579206 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20170615 MGI PMID:27345595 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20170615 MGI PMID:27345595 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:11687615 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001377 abnormal mating frequency IAGP N RGD:5509061 20141003 MGI PMID:12409213 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11687615 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:11687615 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:11687615 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11579206 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:11579206 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:17945412 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:11579206 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11579206 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:23500093 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:11687615 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12409213 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17945412 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12409213 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11579206 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:17945412 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:11687615 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:11579206 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23500093 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:17945412 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11579206 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:17945412 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0005661 decreased circulating adrenaline level IAGP N RGD:5509061 20180927 MGI PMID:11756684 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20170615 MGI PMID:27345595 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17945412 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0009326 absent maternal crouching IAGP N RGD:5509061 20141003 MGI PMID:12409213 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:23500093 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:11579206 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20171228 MGI PMID:12239106 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11579206 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12239106 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11687615 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17945412 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15217792 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:23500093 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:23500093 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0020220 decreased tear production IAGP N RGD:5509061 20170615 MGI PMID:27345595 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:23500093 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:15217792 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:15217792 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0030762 decreased adrenaline level IAGP N RGD:5509061 20180927 MGI PMID:11756684 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:11579206 10084 Adcyap1 adenylate cyclase activating polypeptide 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:15217792 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10792006 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:11483244 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11466423 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11466423 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11193864 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10792006 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11032869 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11466423 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11792830 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20220421 MGI PMID:11466423 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10792006 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:10792006 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:11193864 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:11193864 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10792006 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11466423 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210422 MGI 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:11425915 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0020475 delayed circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:11425915 10085 Adcyap1r1 adenylate cyclase activating polypeptide 1 receptor 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:11483244 10086 Add1 adducin 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18723693 10086 Add1 adducin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18723693 10086 Add1 adducin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18723693 10086 Add1 adducin 1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:18723693 10086 Add1 adducin 1 gene MP:0001893 non-obstructive hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:18723693 10086 Add1 adducin 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18723693 10086 Add1 adducin 1 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:18723693 10086 Add1 adducin 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:18723693 10086 Add1 adducin 1 gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:18723693 10086 Add1 adducin 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:18723693 10086 Add1 adducin 1 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:18723693 10086 Add1 adducin 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:18723693 10086 Add1 adducin 1 gene MP:0008850 increased hemoglobin concentration distribution width IAGP N RGD:5509061 20141003 MGI PMID:18723693 10086 Add1 adducin 1 gene MP:0008935 decreased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:18723693 10086 Add1 adducin 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18723693 10087 Add2 adducin 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:10485892 10087 Add2 adducin 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:10845937 10087 Add2 adducin 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19425068 10087 Add2 adducin 2 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:10988280 10087 Add2 adducin 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10485892 10087 Add2 adducin 2 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15728854 10087 Add2 adducin 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15728854 10087 Add2 adducin 2 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15728854 10087 Add2 adducin 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:15728854 10087 Add2 adducin 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10485892 10087 Add2 adducin 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10845937 10087 Add2 adducin 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19425068 10087 Add2 adducin 2 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:15728854 10087 Add2 adducin 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15728854 10087 Add2 adducin 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19425068 10087 Add2 adducin 2 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:10485892 10087 Add2 adducin 2 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:19425068 10087 Add2 adducin 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:10485892 10087 Add2 adducin 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:10845937 10087 Add2 adducin 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:19425068 10087 Add2 adducin 2 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:10485892 10087 Add2 adducin 2 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:19425068 10087 Add2 adducin 2 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:10845937 10087 Add2 adducin 2 gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:10485892 10087 Add2 adducin 2 gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:19425068 10087 Add2 adducin 2 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:10485892 10087 Add2 adducin 2 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:10845937 10087 Add2 adducin 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:10845937 10087 Add2 adducin 2 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:15728854 10087 Add2 adducin 2 gene MP:0002923 increased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:15728854 10087 Add2 adducin 2 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10485892 10087 Add2 adducin 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:10845937 10087 Add2 adducin 2 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:10845937 10087 Add2 adducin 2 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:10845937 10087 Add2 adducin 2 gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:10485892 10087 Add2 adducin 2 gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:10845937 10087 Add2 adducin 2 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10988280 10087 Add2 adducin 2 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10988280 10087 Add2 adducin 2 gene MP:0006265 increased pulse pressure IAGP N RGD:5509061 20141003 MGI PMID:10988280 10087 Add2 adducin 2 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:10485892 10087 Add2 adducin 2 gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:10485892 10087 Add2 adducin 2 gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20141003 MGI PMID:10485892 10087 Add2 adducin 2 gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:10845937 10087 Add2 adducin 2 gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:19425068 10088 Add3 adducin 3 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19425068 10088 Add3 adducin 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19425068 10088 Add3 adducin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19425068 10088 Add3 adducin 3 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19425068 10088 Add3 adducin 3 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:19425068 10088 Add3 adducin 3 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:19425068 10088 Add3 adducin 3 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:19425068 10088 Add3 adducin 3 gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:19425068 10088 Add3 adducin 3 gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:19425068 10090 Adh1 alcohol dehydrogenase 1 (class I) gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11836246 10090 Adh1 alcohol dehydrogenase 1 (class I) gene MP:0005443 abnormal ethanol metabolism IAGP N RGD:5509061 20141003 MGI PMID:10358022 10090 Adh1 alcohol dehydrogenase 1 (class I) gene MP:0005443 abnormal ethanol metabolism IAGP N RGD:5509061 20231019 MGI PMID:36224745 10090 Adh1 alcohol dehydrogenase 1 (class I) gene MP:0005444 abnormal retinol metabolism IAGP N RGD:5509061 20141003 MGI PMID:10358022 10090 Adh1 alcohol dehydrogenase 1 (class I) gene MP:0005444 abnormal retinol metabolism IAGP N RGD:5509061 20141003 MGI PMID:11836246 10090 Adh1 alcohol dehydrogenase 1 (class I) gene MP:0005444 abnormal retinol metabolism IAGP N RGD:5509061 20141003 MGI PMID:12027900 10090 Adh1 alcohol dehydrogenase 1 (class I) gene MP:0005444 abnormal retinol metabolism IAGP N RGD:5509061 20141003 MGI PMID:12851412 10090 Adh1 alcohol dehydrogenase 1 (class I) gene MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20231019 MGI PMID:10358022 10090 Adh1 alcohol dehydrogenase 1 (class I) gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11836246 10091 Adk adenosine kinase gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:11997462 10091 Adk adenosine kinase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 10091 Adk adenosine kinase gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 10091 Adk adenosine kinase gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 10091 Adk adenosine kinase gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20170119 MGI PMID:27903722 10091 Adk adenosine kinase gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20210826 MGI 10091 Adk adenosine kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11997462 10091 Adk adenosine kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11997462 10091 Adk adenosine kinase gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:11997462 10091 Adk adenosine kinase gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 10091 Adk adenosine kinase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 10091 Adk adenosine kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11997462 10091 Adk adenosine kinase gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11997462 10091 Adk adenosine kinase gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11997462 10091 Adk adenosine kinase gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:11997462 10091 Adk adenosine kinase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 10091 Adk adenosine kinase gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20170119 MGI PMID:27903722 10091 Adk adenosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20170119 MGI PMID:27903722 10091 Adk adenosine kinase gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20170119 MGI PMID:27903722 10091 Adk adenosine kinase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:11997462 10091 Adk adenosine kinase gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20170119 MGI PMID:27903722 10091 Adk adenosine kinase gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20170119 MGI PMID:27903722 10091 Adk adenosine kinase gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20170119 MGI PMID:27903722 10091 Adk adenosine kinase gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:11997462 10091 Adk adenosine kinase gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20210826 MGI 10091 Adk adenosine kinase gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20170119 MGI PMID:27903722 10091 Adk adenosine kinase gene MP:0004882 enlarged lung IEA N RGD:5509061 20210826 MGI 10091 Adk adenosine kinase gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20170119 MGI PMID:27903722 10091 Adk adenosine kinase gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20170119 MGI PMID:27903722 10091 Adk adenosine kinase gene MP:0011047 increased lung tissue damping IEA N RGD:5509061 20211021 MGI 10091 Adk adenosine kinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11997462 10091 Adk adenosine kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 10091 Adk adenosine kinase gene MP:0012348 decreased susceptibility to induction of seizure by inducing agent IAGP N RGD:5509061 20170119 MGI PMID:27903722 10091 Adk adenosine kinase gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:11997462 10091 Adk adenosine kinase gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:11997462 10092 Adora2a adenosine A2a receptor gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230601 MGI 10092 Adora2a adenosine A2a receptor gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20938208 10092 Adora2a adenosine A2a receptor gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:20938208 10092 Adora2a adenosine A2a receptor gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:9262401 10092 Adora2a adenosine A2a receptor gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:9262401 10092 Adora2a adenosine A2a receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10531422 10092 Adora2a adenosine A2a receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10771351 10092 Adora2a adenosine A2a receptor gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:9262401 10092 Adora2a adenosine A2a receptor gene MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20141003 MGI PMID:16129427 10092 Adora2a adenosine A2a receptor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:9262401 10092 Adora2a adenosine A2a receptor gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:9262401 10092 Adora2a adenosine A2a receptor gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:9262401 10092 Adora2a adenosine A2a receptor gene MP:0002698 abnormal sclera morphology IAGP N RGD:5509061 20141003 MGI PMID:20484596 10092 Adora2a adenosine A2a receptor gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9262401 10092 Adora2a adenosine A2a receptor gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210128 MGI 10092 Adora2a adenosine A2a receptor gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20210826 MGI 10092 Adora2a adenosine A2a receptor gene MP:0002975 vascular smooth muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20938208 10092 Adora2a adenosine A2a receptor gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:9262401 10092 Adora2a adenosine A2a receptor gene MP:0003100 myopia IAGP N RGD:5509061 20141003 MGI PMID:20484596 10092 Adora2a adenosine A2a receptor gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:15602504 10092 Adora2a adenosine A2a receptor gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16280580 10092 Adora2a adenosine A2a receptor gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:9262401 10092 Adora2a adenosine A2a receptor gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20141003 MGI PMID:20938208 10092 Adora2a adenosine A2a receptor gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220811 MGI 10092 Adora2a adenosine A2a receptor gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20938208 10092 Adora2a adenosine A2a receptor gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 10092 Adora2a adenosine A2a receptor gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20210826 MGI 10092 Adora2a adenosine A2a receptor gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20211021 MGI 10092 Adora2a adenosine A2a receptor gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:10531422 10092 Adora2a adenosine A2a receptor gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:10531422 10092 Adora2a adenosine A2a receptor gene MP:0006087 increased body mass index IAGP N RGD:5509061 20141003 MGI PMID:9262401 10092 Adora2a adenosine A2a receptor gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:17525287 10092 Adora2a adenosine A2a receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12700712 10092 Adora2a adenosine A2a receptor gene MP:0009586 increased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:9262401 10092 Adora2a adenosine A2a receptor gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:10771351 10092 Adora2a adenosine A2a receptor gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:12700712 10092 Adora2a adenosine A2a receptor gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:15602504 10092 Adora2a adenosine A2a receptor gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:15965471 10092 Adora2a adenosine A2a receptor gene MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:11166335 10092 Adora2a adenosine A2a receptor gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 10092 Adora2a adenosine A2a receptor gene MP:0010758 increased right ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:20938208 10092 Adora2a adenosine A2a receptor gene MP:0012348 decreased susceptibility to induction of seizure by inducing agent IAGP N RGD:5509061 20170119 MGI PMID:27903722 10092 Adora2a adenosine A2a receptor gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 10093 Adora3 adenosine A3 receptor gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:12817015 10093 Adora3 adenosine A3 receptor gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10660615 10093 Adora3 adenosine A3 receptor gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20150101 MGI PMID:16157310 10093 Adora3 adenosine A3 receptor gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:12220556 10093 Adora3 adenosine A3 receptor gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10699369 10093 Adora3 adenosine A3 receptor gene MP:0003022 increased coronary flow rate IAGP N RGD:5509061 20141003 MGI PMID:12003827 10093 Adora3 adenosine A3 receptor gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:11273734 10093 Adora3 adenosine A3 receptor gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:10699369 10093 Adora3 adenosine A3 receptor gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:12003827 10093 Adora3 adenosine A3 receptor gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:12817015 10093 Adora3 adenosine A3 receptor gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:12388399 10093 Adora3 adenosine A3 receptor gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:12220556 10093 Adora3 adenosine A3 receptor gene MP:0005260 ocular hypotension IAGP N RGD:5509061 20141003 MGI PMID:12202525 10093 Adora3 adenosine A3 receptor gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:12388399 10093 Adora3 adenosine A3 receptor gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:10660615 10093 Adora3 adenosine A3 receptor gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:12817015 10093 Adora3 adenosine A3 receptor gene MP:0008763 abnormal mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:12817015 10093 Adora3 adenosine A3 receptor gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20150101 MGI PMID:16157310 10094 Adprh ADP-ribosylarginine hydrolase gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:17526733 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9326654 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17951539 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:17951539 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17951539 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:17951539 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:11222061 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:11115730 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11222061 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12782680 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:14581480 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:17951539 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17951539 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17951539 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17951539 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:11222061 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14581480 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14581480 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:12782680 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17951539 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:14581480 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17951539 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17951539 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12782680 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15466664 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14519431 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:15466664 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:12782680 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:12782680 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:11222061 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14581480 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0003823 increased left ventricle developed pressure IAGP N RGD:5509061 20141003 MGI PMID:14519431 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15466664 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:11115730 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0004184 abnormal baroreceptor physiology IAGP N RGD:5509061 20141003 MGI PMID:15466664 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:14519431 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:12782680 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:12782680 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17951539 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:17951539 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15466664 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9326654 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:14581480 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:14581480 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12782680 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15466664 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20141003 MGI PMID:12782680 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:14581480 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:14581480 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:14581480 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:12782680 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15466664 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17951539 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:11923452 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:11923452 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12782680 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20160310 MGI PMID:14581480 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20160310 MGI PMID:14581480 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:12782680 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:12782680 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0014269 decreased testes secretion IAGP N RGD:5509061 20230810 MGI PMID:17951539 10096 Adra1b adrenergic receptor, alpha 1b gene MP:0031635 increased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:12782680 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:17992256 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10385696 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:8670421 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20170105 MGI 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10647009 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:12068299 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:12068299 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17992256 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20190110 MGI 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19276088 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:10385696 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20160211 MGI 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12068299 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0005447 abnormal synaptic norepinephrine release IAGP N RGD:5509061 20141003 MGI PMID:10647009 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20190110 MGI 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:19225179 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12068299 10098 Adra2a adrenergic receptor, alpha 2a gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20160211 MGI 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:8670422 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:20729197 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:20729197 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:20729197 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:20729197 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:12068299 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:12068299 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:20729197 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8670422 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:10647009 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:8670422 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:20729197 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:20729197 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12068299 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:20729197 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:20729197 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:20729197 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20729197 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12068299 10101 Adra2b adrenergic receptor, alpha 2b gene MP:0011147 increased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:20729197 10103 Adra2c adrenergic receptor, alpha 2c gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:9526020 10103 Adra2c adrenergic receptor, alpha 2c gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10647009 10103 Adra2c adrenergic receptor, alpha 2c gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:12068299 10103 Adra2c adrenergic receptor, alpha 2c gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:12068299 10103 Adra2c adrenergic receptor, alpha 2c gene MP:0003063 increased coping response IAGP N RGD:5509061 20151119 MGI PMID:10523817 10103 Adra2c adrenergic receptor, alpha 2c gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12068299 10103 Adra2c adrenergic receptor, alpha 2c gene MP:0005447 abnormal synaptic norepinephrine release IAGP N RGD:5509061 20141003 MGI PMID:10647009 10103 Adra2c adrenergic receptor, alpha 2c gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:10051760 10103 Adra2c adrenergic receptor, alpha 2c gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:11642653 10103 Adra2c adrenergic receptor, alpha 2c gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12068299 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12161655 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12161655 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:10358009 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:8693001 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12161655 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:10358009 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10358009 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:10358009 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:12161655 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:10358009 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12161655 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10358009 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:8693001 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0009119 increased brown fat cell size IAGP N RGD:5509061 20141003 MGI PMID:12161655 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12161655 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12161655 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:12161655 10106 Adrb1 adrenergic receptor, beta 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8693001 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12161655 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12161655 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:9276726 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12161655 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:12161655 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:9276726 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:9276726 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12161655 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:7493988 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0009119 increased brown fat cell size IAGP N RGD:5509061 20141003 MGI PMID:12161655 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12161655 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0009300 increased parametrial fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:7493988 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12161655 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:7493988 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:9276726 10110 Adrb3 adrenergic receptor, beta 3 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:12161655 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17008600 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17008600 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:17008600 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17008600 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21960637 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21960637 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17008600 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0004055 heart atrium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0004062 dilated heart right atrium IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17008600 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17008600 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17008600 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8917529 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:21960637 10111 Grk2 G protein-coupled receptor kinase 2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:8917529 10112 Grk3 G protein-coupled receptor kinase 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 10112 Grk3 G protein-coupled receptor kinase 3 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:9325250 10112 Grk3 G protein-coupled receptor kinase 3 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 10117 Agrn agrin gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:21890498 10117 Agrn agrin gene MP:0000743 muscle spasm IEA N RGD:5509061 20111116 MGI 10117 Agrn agrin gene MP:0000745 tremors IEA N RGD:5509061 20111116 MGI 10117 Agrn agrin gene MP:0000751 myopathy IEA N RGD:5509061 20111116 MGI 10117 Agrn agrin gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:8653788 10117 Agrn agrin gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:10402191 10117 Agrn agrin gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:11431694 10117 Agrn agrin gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:17591961 10117 Agrn agrin gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:21890498 10117 Agrn agrin gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:8653788 10117 Agrn agrin gene MP:0001054 failure of neuromuscular synapse presynaptic differentiation IAGP N RGD:5509061 20141003 MGI PMID:20498043 10117 Agrn agrin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21890498 10117 Agrn agrin gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:10402191 10117 Agrn agrin gene MP:0001513 limb grasping IEA N RGD:5509061 20111116 MGI 10117 Agrn agrin gene MP:0001524 impaired limb coordination IEA N RGD:5509061 20111116 MGI 10117 Agrn agrin gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20151112 MGI PMID:22082664 10117 Agrn agrin gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10402191 10117 Agrn agrin gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:21890498 10117 Agrn agrin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21890498 10117 Agrn agrin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10402191 10117 Agrn agrin gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:10402191 10117 Agrn agrin gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:8653788 10117 Agrn agrin gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:17591961 10117 Agrn agrin gene MP:0002923 increased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:12221070 10117 Agrn agrin gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20151112 MGI PMID:22082664 10117 Agrn agrin gene MP:0003807 camptodactyly IEA N RGD:5509061 20111116 MGI 10117 Agrn agrin gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:12221070 10117 Agrn agrin gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:12221070 10117 Agrn agrin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:8653788 10117 Agrn agrin gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:21890498 10117 Agrn agrin gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:21890498 10117 Agrn agrin gene MP:0009434 paraparesis IEA N RGD:5509061 20111116 MGI 10117 Agrn agrin gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:10402191 10117 Agrn agrin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11431694 10117 Agrn agrin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10402191 10117 Agrn agrin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17591961 10117 Agrn agrin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8653788 10117 Agrn agrin gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17591961 10117 Agrn agrin gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:17591961 10118 Agt angiotensinogen gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:11606482 10118 Agt angiotensinogen gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:8941219 10118 Agt angiotensinogen gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:7708716 10118 Agt angiotensinogen gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:8941219 10118 Agt angiotensinogen gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11606482 10118 Agt angiotensinogen gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7989296 10118 Agt angiotensinogen gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:11606482 10118 Agt angiotensinogen gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:7989296 10118 Agt angiotensinogen gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:8941219 10118 Agt angiotensinogen gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:11606482 10118 Agt angiotensinogen gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:8941219 10118 Agt angiotensinogen gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:18497303 10118 Agt angiotensinogen gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:9507206 10118 Agt angiotensinogen gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0002829 abnormal juxtaglomerular apparatus morphology IAGP N RGD:5509061 20141003 MGI PMID:11606482 10118 Agt angiotensinogen gene MP:0002829 abnormal juxtaglomerular apparatus morphology IAGP N RGD:5509061 20141003 MGI PMID:8941219 10118 Agt angiotensinogen gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7708716 10118 Agt angiotensinogen gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7708716 10118 Agt angiotensinogen gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7989296 10118 Agt angiotensinogen gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9466969 10118 Agt angiotensinogen gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:9507206 10118 Agt angiotensinogen gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:7708716 10118 Agt angiotensinogen gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:11606482 10118 Agt angiotensinogen gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:7708716 10118 Agt angiotensinogen gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:8941219 10118 Agt angiotensinogen gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:7708716 10118 Agt angiotensinogen gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:9042165 10118 Agt angiotensinogen gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:9507206 10118 Agt angiotensinogen gene MP:0005489 vascular smooth muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8941219 10118 Agt angiotensinogen gene MP:0005502 abnormal renal/urinary system physiology IAGP N RGD:5509061 20141003 MGI PMID:9507206 10118 Agt angiotensinogen gene MP:0005525 increased renal plasma flow rate IAGP N RGD:5509061 20141003 MGI PMID:7708716 10118 Agt angiotensinogen gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:9507206 10118 Agt angiotensinogen gene MP:0005556 abnormal renal filtration rate IAGP N RGD:5509061 20141003 MGI PMID:9507206 10118 Agt angiotensinogen gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0005610 increased circulating antidiuretic hormone level IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7989296 10118 Agt angiotensinogen gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11606482 10118 Agt angiotensinogen gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22071160 10118 Agt angiotensinogen gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7989296 10118 Agt angiotensinogen gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0006375 increased circulating angiotensinogen level IAGP N RGD:5509061 20141003 MGI PMID:7708716 10118 Agt angiotensinogen gene MP:0006375 increased circulating angiotensinogen level IAGP N RGD:5509061 20141003 MGI PMID:8170956 10118 Agt angiotensinogen gene MP:0006376 decreased circulating angiotensinogen level IAGP N RGD:5509061 20141003 MGI PMID:11606482 10118 Agt angiotensinogen gene MP:0006376 decreased circulating angiotensinogen level IAGP N RGD:5509061 20141003 MGI PMID:22071160 10118 Agt angiotensinogen gene MP:0006376 decreased circulating angiotensinogen level IAGP N RGD:5509061 20141003 MGI PMID:7708716 10118 Agt angiotensinogen gene MP:0006376 decreased circulating angiotensinogen level IAGP N RGD:5509061 20141003 MGI PMID:7989296 10118 Agt angiotensinogen gene MP:0006376 decreased circulating angiotensinogen level IAGP N RGD:5509061 20141003 MGI PMID:8170956 10118 Agt angiotensinogen gene MP:0008285 abnormal hippocampus granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:10617578 10118 Agt angiotensinogen gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:11606482 10118 Agt angiotensinogen gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11606482 10118 Agt angiotensinogen gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11606482 10118 Agt angiotensinogen gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7989296 10118 Agt angiotensinogen gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11606482 10118 Agt angiotensinogen gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7708716 10118 Agt angiotensinogen gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20141003 MGI PMID:11606482 10118 Agt angiotensinogen gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20141003 MGI PMID:8941219 10118 Agt angiotensinogen gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0011312 abnormal kidney afferent arteriole morphology IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0011312 abnormal kidney afferent arteriole morphology IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0011314 abnormal kidney cortex artery morphology IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0011316 abnormal kidney interlobular artery morphology IAGP N RGD:5509061 20141003 MGI PMID:7708716 10118 Agt angiotensinogen gene MP:0011316 abnormal kidney interlobular artery morphology IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0011316 abnormal kidney interlobular artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0011333 abnormal kidney inner medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:11606482 10118 Agt angiotensinogen gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:7708716 10118 Agt angiotensinogen gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:7708716 10118 Agt angiotensinogen gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0011422 kidney medulla atrophy IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20141003 MGI PMID:7708716 10118 Agt angiotensinogen gene MP:0011431 increased urine flow rate IAGP N RGD:5509061 20141003 MGI PMID:9507206 10118 Agt angiotensinogen gene MP:0011541 decreased urine aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0011543 increased urine antidiuretic hormone level IAGP N RGD:5509061 20141003 MGI PMID:9507198 10118 Agt angiotensinogen gene MP:0011565 kidney papillary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8675666 10118 Agt angiotensinogen gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:9507206 10118 Agt angiotensinogen gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:10617578 10118 Agt angiotensinogen gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:11606482 10118 Agt angiotensinogen gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:11384650 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20170209 MGI PMID:9466969 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20170209 MGI PMID:9466969 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20170209 MGI PMID:10432390 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20170209 MGI PMID:9466969 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20170209 MGI PMID:9466969 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20170209 MGI PMID:9466969 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0003675 kidney cyst IAGP N RGD:5509061 20170209 MGI PMID:15306694 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0003675 kidney cyst IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20170209 MGI PMID:9466969 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0005583 decreased renin activity IAGP N RGD:5509061 20170209 MGI PMID:15306694 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20170209 MGI PMID:9466969 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20170209 MGI PMID:9466969 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20170209 MGI PMID:9466969 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:9466969 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0011305 dilated kidney calyx IAGP N RGD:5509061 20170209 MGI PMID:9466969 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0011306 absent kidney pelvis IAGP N RGD:5509061 20170209 MGI PMID:10432390 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20170209 MGI PMID:18497303 10123 Agtr1b angiotensin II receptor, type 1b gene MP:0011565 kidney papillary hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:9466969 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10373225 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12388241 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15793237 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7477266 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:10373225 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10930448 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:12390955 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:12624001 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9551401 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20141003 MGI PMID:11384784 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:11384784 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:7477266 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:7477267 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:15793237 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:7477267 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15793237 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:10373225 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:12218346 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:12218346 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:19033539 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0001948 vesicoureteral reflux IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15793237 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15793237 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:12624001 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12154115 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7477267 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15793237 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0002975 vascular smooth muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11714657 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:11714657 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:7477267 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10930448 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12390955 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9551401 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003334 pancreas fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19033539 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:7477267 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003585 large ureter IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003586 dilated ureter IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003600 ectopic kidney IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:15793237 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003916 decreased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:12390955 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12390955 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:12218346 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0004082 abnormal habenula morphology IAGP N RGD:5509061 20141003 MGI PMID:11384784 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:15793237 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0004184 abnormal baroreceptor physiology IAGP N RGD:5509061 20141003 MGI PMID:12154115 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:10930448 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16140932 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12154115 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:15793237 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20200416 MGI PMID:16001071 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0005502 abnormal renal/urinary system physiology IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0005526 decreased renal plasma flow rate IAGP N RGD:5509061 20141003 MGI PMID:10620200 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0005531 increased renal vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:10620200 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:7477267 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10373225 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14597675 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14597675 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15793237 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0005667 abnormal circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15793237 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7477267 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12388241 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7477267 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0006274 abnormal urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:10620200 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15793237 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:11384784 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0008265 abnormal hippocampus CA2 region morphology IAGP N RGD:5509061 20141003 MGI PMID:11384784 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:11384784 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12154115 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19033539 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0009109 decreased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:19033539 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0009130 increased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:15793237 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:15793237 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0009150 pancreatic acinar cell atrophy IAGP N RGD:5509061 20141003 MGI PMID:19033539 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:19004830 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10620200 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12390955 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12624001 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20141009 MGI PMID:23636094 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0010009 abnormal piriform cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11384784 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:15793237 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0010661 ascending aorta aneurysm IAGP N RGD:5509061 20141009 MGI PMID:23636094 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:10930448 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:19004830 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:19004830 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:19004830 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0010932 increased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:19004830 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20141009 MGI PMID:23636094 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0011371 decreased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9551401 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0011415 abnormal aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:12218346 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0011489 ureteropelvic junction atresia IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0011490 ureteropelvic junction stenosis IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0011492 ureterovesical junction obstruction IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0011493 double ureter IAGP N RGD:5509061 20141003 MGI PMID:10024874 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:18497303 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:12388241 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0011947 abnormal fluid intake IAGP N RGD:5509061 20141003 MGI PMID:7477266 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:12218346 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:10930448 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0030761 increased adrenaline level IAGP N RGD:5509061 20180927 MGI PMID:12218346 10126 Agtr2 angiotensin II receptor, type 2 gene MP:0031413 abnormal skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:15793237 10127 Ahr aryl-hydrocarbon receptor gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8692887 10127 Ahr aryl-hydrocarbon receptor gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:18660548 10127 Ahr aryl-hydrocarbon receptor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0000376 folliculitis IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0000405 abnormal auchene hair morphology IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10973493 10127 Ahr aryl-hydrocarbon receptor gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:22232670 10127 Ahr aryl-hydrocarbon receptor gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22232670 10127 Ahr aryl-hydrocarbon receptor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:7732381 10127 Ahr aryl-hydrocarbon receptor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:18660548 10127 Ahr aryl-hydrocarbon receptor gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:8692887 10127 Ahr aryl-hydrocarbon receptor gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:8692887 10127 Ahr aryl-hydrocarbon receptor gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10973493 10127 Ahr aryl-hydrocarbon receptor gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7732381 10127 Ahr aryl-hydrocarbon receptor gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:7732381 10127 Ahr aryl-hydrocarbon receptor gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:9772216 10127 Ahr aryl-hydrocarbon receptor gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18660548 10127 Ahr aryl-hydrocarbon receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:8692887 10127 Ahr aryl-hydrocarbon receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:7732381 10127 Ahr aryl-hydrocarbon receptor gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7732381 10127 Ahr aryl-hydrocarbon receptor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:12606443 10127 Ahr aryl-hydrocarbon receptor gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:12606443 10127 Ahr aryl-hydrocarbon receptor gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:24174576 10127 Ahr aryl-hydrocarbon receptor gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12151645 10127 Ahr aryl-hydrocarbon receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8692887 10127 Ahr aryl-hydrocarbon receptor gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20829355 10127 Ahr aryl-hydrocarbon receptor gene MP:0001326 retina degeneration IAGP N RGD:5509061 20181011 MGI PMID:29726989 10127 Ahr aryl-hydrocarbon receptor gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:23301081 10127 Ahr aryl-hydrocarbon receptor gene MP:0001573 abnormal circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20829355 10127 Ahr aryl-hydrocarbon receptor gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0001665 chronic diarrhea IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7732381 10127 Ahr aryl-hydrocarbon receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8692887 10127 Ahr aryl-hydrocarbon receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9427285 10127 Ahr aryl-hydrocarbon receptor gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:4750810 10127 Ahr aryl-hydrocarbon receptor gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:4750810 10127 Ahr aryl-hydrocarbon receptor gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:5132702 10127 Ahr aryl-hydrocarbon receptor gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:7732381 10127 Ahr aryl-hydrocarbon receptor gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:15123765 10127 Ahr aryl-hydrocarbon receptor gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17322371 10127 Ahr aryl-hydrocarbon receptor gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20141003 MGI PMID:12606443 10127 Ahr aryl-hydrocarbon receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:16291824 10127 Ahr aryl-hydrocarbon receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10910997 10127 Ahr aryl-hydrocarbon receptor gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17322371 10127 Ahr aryl-hydrocarbon receptor gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17322371 10127 Ahr aryl-hydrocarbon receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12646173 10127 Ahr aryl-hydrocarbon receptor gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:24174576 10127 Ahr aryl-hydrocarbon receptor gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:10910997 10127 Ahr aryl-hydrocarbon receptor gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12621046 10127 Ahr aryl-hydrocarbon receptor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0002975 vascular smooth muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:19454665 10127 Ahr aryl-hydrocarbon receptor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0003254 bile duct inflammation IAGP N RGD:5509061 20141003 MGI PMID:7732381 10127 Ahr aryl-hydrocarbon receptor gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:7732381 10127 Ahr aryl-hydrocarbon receptor gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:10973493 10127 Ahr aryl-hydrocarbon receptor gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:12621046 10127 Ahr aryl-hydrocarbon receptor gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:7732381 10127 Ahr aryl-hydrocarbon receptor gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19454665 10127 Ahr aryl-hydrocarbon receptor gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20141003 MGI PMID:10614669 10127 Ahr aryl-hydrocarbon receptor gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20141003 MGI PMID:17594909 10127 Ahr aryl-hydrocarbon receptor gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20200903 MGI PMID:31606043 10127 Ahr aryl-hydrocarbon receptor gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:15123765 10127 Ahr aryl-hydrocarbon receptor gene MP:0004004 patent ductus venosus IAGP N RGD:5509061 20141003 MGI PMID:10973493 10127 Ahr aryl-hydrocarbon receptor gene MP:0004004 patent ductus venosus IAGP N RGD:5509061 20141003 MGI PMID:12621046 10127 Ahr aryl-hydrocarbon receptor gene MP:0004004 patent ductus venosus IAGP N RGD:5509061 20141003 MGI PMID:15545609 10127 Ahr aryl-hydrocarbon receptor gene MP:0004004 patent ductus venosus IAGP N RGD:5509061 20141003 MGI PMID:16301529 10127 Ahr aryl-hydrocarbon receptor gene MP:0004004 patent ductus venosus IAGP N RGD:5509061 20141003 MGI PMID:18660548 10127 Ahr aryl-hydrocarbon receptor gene MP:0004004 patent ductus venosus IAGP N RGD:5509061 20141003 MGI PMID:20829355 10127 Ahr aryl-hydrocarbon receptor gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20181011 MGI PMID:29726989 10127 Ahr aryl-hydrocarbon receptor gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20141003 MGI PMID:24174576 10127 Ahr aryl-hydrocarbon receptor gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16704990 10127 Ahr aryl-hydrocarbon receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:24174576 10127 Ahr aryl-hydrocarbon receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:17594909 10127 Ahr aryl-hydrocarbon receptor gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:12151645 10127 Ahr aryl-hydrocarbon receptor gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:24174576 10127 Ahr aryl-hydrocarbon receptor gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:12621046 10127 Ahr aryl-hydrocarbon receptor gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20200903 MGI PMID:31606043 10127 Ahr aryl-hydrocarbon receptor gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8692887 10127 Ahr aryl-hydrocarbon receptor gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:15123765 10127 Ahr aryl-hydrocarbon receptor gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19454665 10127 Ahr aryl-hydrocarbon receptor gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12151645 10127 Ahr aryl-hydrocarbon receptor gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:24174576 10127 Ahr aryl-hydrocarbon receptor gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:15123765 10127 Ahr aryl-hydrocarbon receptor gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:19454665 10127 Ahr aryl-hydrocarbon receptor gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20200903 MGI PMID:31606043 10127 Ahr aryl-hydrocarbon receptor gene MP:0008117 abnormal Langerhans cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19454665 10127 Ahr aryl-hydrocarbon receptor gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24174576 10127 Ahr aryl-hydrocarbon receptor gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20181011 MGI PMID:29726989 10127 Ahr aryl-hydrocarbon receptor gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:8692887 10127 Ahr aryl-hydrocarbon receptor gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20181011 MGI PMID:29726989 10127 Ahr aryl-hydrocarbon receptor gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20181011 MGI PMID:29726989 10127 Ahr aryl-hydrocarbon receptor gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20181011 MGI PMID:29726989 10127 Ahr aryl-hydrocarbon receptor gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:17322371 10127 Ahr aryl-hydrocarbon receptor gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:17322371 10127 Ahr aryl-hydrocarbon receptor gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:17322371 10127 Ahr aryl-hydrocarbon receptor gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17322371 10127 Ahr aryl-hydrocarbon receptor gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:12646173 10127 Ahr aryl-hydrocarbon receptor gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12730383 10127 Ahr aryl-hydrocarbon receptor gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16291824 10127 Ahr aryl-hydrocarbon receptor gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16704990 10127 Ahr aryl-hydrocarbon receptor gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17322371 10127 Ahr aryl-hydrocarbon receptor gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:6021513 10127 Ahr aryl-hydrocarbon receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12151645 10127 Ahr aryl-hydrocarbon receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12621046 10127 Ahr aryl-hydrocarbon receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12730383 10127 Ahr aryl-hydrocarbon receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15545609 10127 Ahr aryl-hydrocarbon receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16291824 10127 Ahr aryl-hydrocarbon receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16301529 10127 Ahr aryl-hydrocarbon receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18660548 10127 Ahr aryl-hydrocarbon receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20829355 10127 Ahr aryl-hydrocarbon receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:6021513 10127 Ahr aryl-hydrocarbon receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:7732381 10127 Ahr aryl-hydrocarbon receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:8806883 10127 Ahr aryl-hydrocarbon receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9427285 10127 Ahr aryl-hydrocarbon receptor gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:12646173 10127 Ahr aryl-hydrocarbon receptor gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20141003 MGI PMID:10973493 10127 Ahr aryl-hydrocarbon receptor gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:24174576 10127 Ahr aryl-hydrocarbon receptor gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:24174576 10127 Ahr aryl-hydrocarbon receptor gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22232670 10127 Ahr aryl-hydrocarbon receptor gene MP:0009600 hypergranulosis IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20141003 MGI PMID:23301081 10127 Ahr aryl-hydrocarbon receptor gene MP:0009646 urinary bladder inflammation IAGP N RGD:5509061 20141003 MGI PMID:22232670 10127 Ahr aryl-hydrocarbon receptor gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:24174576 10127 Ahr aryl-hydrocarbon receptor gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16291824 10127 Ahr aryl-hydrocarbon receptor gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16704990 10127 Ahr aryl-hydrocarbon receptor gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:6021513 10127 Ahr aryl-hydrocarbon receptor gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16291824 10127 Ahr aryl-hydrocarbon receptor gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:6021513 10127 Ahr aryl-hydrocarbon receptor gene MP:0009810 increased urine uric acid level IAGP N RGD:5509061 20141003 MGI PMID:22232670 10127 Ahr aryl-hydrocarbon receptor gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17052998 10127 Ahr aryl-hydrocarbon receptor gene MP:0010785 abnormal stomach pyloric region morphology IAGP N RGD:5509061 20141003 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0010894 pulmonary alveolar edema IAGP N RGD:5509061 20141003 MGI PMID:15123765 10127 Ahr aryl-hydrocarbon receptor gene MP:0011042 abnormal horizontal vestibuloocular reflex IAGP N RGD:5509061 20141003 MGI PMID:23301081 10127 Ahr aryl-hydrocarbon receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12646173 10127 Ahr aryl-hydrocarbon receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7732381 10127 Ahr aryl-hydrocarbon receptor gene MP:0011120 increased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10614669 10127 Ahr aryl-hydrocarbon receptor gene MP:0011120 increased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10910997 10127 Ahr aryl-hydrocarbon receptor gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10910997 10127 Ahr aryl-hydrocarbon receptor gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:12606443 10127 Ahr aryl-hydrocarbon receptor gene MP:0011625 cystolithiasis IAGP N RGD:5509061 20141003 MGI PMID:22232670 10127 Ahr aryl-hydrocarbon receptor gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24174576 10127 Ahr aryl-hydrocarbon receptor gene MP:0011769 urinary bladder fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22232670 10127 Ahr aryl-hydrocarbon receptor gene MP:0011773 abnormal urinary bladder vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22232670 10127 Ahr aryl-hydrocarbon receptor gene MP:0012538 persistent hyaloid artery IAGP N RGD:5509061 20141003 MGI PMID:10973493 10127 Ahr aryl-hydrocarbon receptor gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:24174576 10127 Ahr aryl-hydrocarbon receptor gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20181011 MGI PMID:29726989 10127 Ahr aryl-hydrocarbon receptor gene MP:0030571 dilated piliary canal IAGP N RGD:5509061 20180524 MGI PMID:9396142 10127 Ahr aryl-hydrocarbon receptor gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:18660548 10127 Ahr aryl-hydrocarbon receptor gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:8692887 10127 Ahr aryl-hydrocarbon receptor gene MP:0031346 abnormal eye vasculature morphology IAGP N RGD:5509061 20220217 MGI PMID:10973493 10127 Ahr aryl-hydrocarbon receptor gene MP:0031359 decreased prostate gland anterior lobe weight IAGP N RGD:5509061 20220303 MGI PMID:12151645 10127 Ahr aryl-hydrocarbon receptor gene MP:0031366 decreased prostate gland dorsolateral lobe weight IAGP N RGD:5509061 20220303 MGI PMID:12151645 10127 Ahr aryl-hydrocarbon receptor gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10910997 10127 Ahr aryl-hydrocarbon receptor gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:12606443 10127 Ahr aryl-hydrocarbon receptor gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:17594909 10128 Ahsg alpha-2-HS-glycoprotein gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20231207 MGI 10128 Ahsg alpha-2-HS-glycoprotein gene MP:0001314 cornea opacity IEA N RGD:5509061 20231207 MGI 10128 Ahsg alpha-2-HS-glycoprotein gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12145157 10128 Ahsg alpha-2-HS-glycoprotein gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12145157 10128 Ahsg alpha-2-HS-glycoprotein gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12145157 10128 Ahsg alpha-2-HS-glycoprotein gene MP:0002764 short tibia IEA N RGD:5509061 20160114 MGI 10128 Ahsg alpha-2-HS-glycoprotein gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12145157 10128 Ahsg alpha-2-HS-glycoprotein gene MP:0003199 calcified muscle IAGP N RGD:5509061 20141003 MGI PMID:9395485 10128 Ahsg alpha-2-HS-glycoprotein gene MP:0004222 iris synechia IEA N RGD:5509061 20231207 MGI 10128 Ahsg alpha-2-HS-glycoprotein gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 10128 Ahsg alpha-2-HS-glycoprotein gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12145157 10128 Ahsg alpha-2-HS-glycoprotein gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:12145157 10128 Ahsg alpha-2-HS-glycoprotein gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9395485 10128 Ahsg alpha-2-HS-glycoprotein gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:12145157 10129 Ak1 adenylate kinase 1 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:12124227 10129 Ak1 adenylate kinase 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11101510 10129 Ak1 adenylate kinase 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11101510 10129 Ak1 adenylate kinase 1 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:11101510 10129 Ak1 adenylate kinase 1 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:12730234 10129 Ak1 adenylate kinase 1 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:11101510 10129 Ak1 adenylate kinase 1 gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12730234 10129 Ak1 adenylate kinase 1 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:12730234 10129 Ak1 adenylate kinase 1 gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20141003 MGI PMID:11101510 10130 Ak2 adenylate kinase 2 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20210603 MGI PMID:33571905 10130 Ak2 adenylate kinase 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20210603 MGI PMID:33571905 10130 Ak2 adenylate kinase 2 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20210603 MGI PMID:33571905 10130 Ak2 adenylate kinase 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20210603 MGI PMID:33571905 10130 Ak2 adenylate kinase 2 gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20210603 MGI PMID:33571905 10130 Ak2 adenylate kinase 2 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20210603 MGI PMID:33571905 10130 Ak2 adenylate kinase 2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:33571905 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12782654 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:12782654 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:12782654 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20150709 MGI PMID:20837017 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12782654 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:22275470 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:16923958 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:12782654 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:12782654 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001238 thin epidermis stratum spinosum IAGP N RGD:5509061 20141003 MGI PMID:12782654 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12843127 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12843127 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16923958 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19883618 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16923958 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:11387480 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12843127 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16923958 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19289493 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:20348245 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19289493 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17442925 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17442925 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17210696 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12782654 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:22275470 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12843127 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11387480 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12843127 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16923958 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19289493 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19883618 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12782654 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12782654 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19883618 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17442925 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:16923958 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20150709 MGI PMID:20837017 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12782654 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:22275470 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12843127 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19289493 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:16923958 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:22275470 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19289493 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:12843127 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:19289493 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19883618 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16923958 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442925 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442925 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19883618 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11387480 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12843127 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16923958 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19289493 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20348245 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11387480 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12843127 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:16923958 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:19289493 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:19289493 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19883618 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19883618 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19883618 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19289493 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17442925 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0009167 increased pancreatic islet number IAGP N RGD:5509061 20170803 MGI PMID:11387480 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19289493 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19883618 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20348245 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0009371 increased theca cell number IAGP N RGD:5509061 20141003 MGI PMID:22275470 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:12782654 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:12782654 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20150709 MGI PMID:20837017 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16923958 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:12843127 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:12843127 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:11387480 10132 Akt2 thymoma viral proto-oncogene 2 gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:11387480 10133 Alad aminolevulinate, delta-, dehydratase gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210520 MGI 10133 Alad aminolevulinate, delta-, dehydratase gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20240523 MGI 10133 Alad aminolevulinate, delta-, dehydratase gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20240523 MGI 10133 Alad aminolevulinate, delta-, dehydratase gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210520 MGI 10133 Alad aminolevulinate, delta-, dehydratase gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20240523 MGI 10133 Alad aminolevulinate, delta-, dehydratase gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20240523 MGI 10133 Alad aminolevulinate, delta-, dehydratase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20240523 MGI 10133 Alad aminolevulinate, delta-, dehydratase gene MP:0002768 small adrenal glands IEA N RGD:5509061 20210520 MGI 10133 Alad aminolevulinate, delta-, dehydratase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200402 MGI 10133 Alad aminolevulinate, delta-, dehydratase gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20221215 MGI 10133 Alad aminolevulinate, delta-, dehydratase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 10133 Alad aminolevulinate, delta-, dehydratase gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210520 MGI 10133 Alad aminolevulinate, delta-, dehydratase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 10133 Alad aminolevulinate, delta-, dehydratase gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 10136 Alb albumin gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20240222 MGI PMID:37451670 10136 Alb albumin gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20180719 MGI PMID:23549084 10136 Alb albumin gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20180719 MGI PMID:22527485 10136 Alb albumin gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20191205 MGI PMID:25453901 10136 Alb albumin gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180719 MGI PMID:21109326 10136 Alb albumin gene MP:0000603 pale liver IAGP N RGD:5509061 20180719 MGI PMID:21109326 10136 Alb albumin gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20221229 MGI PMID:29967292 10136 Alb albumin gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180719 MGI PMID:21109326 10136 Alb albumin gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20240222 MGI PMID:37451670 10136 Alb albumin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20180719 MGI PMID:21109326 10136 Alb albumin gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20191205 MGI PMID:25453901 10136 Alb albumin gene MP:0001762 polyuria IAGP N RGD:5509061 20180719 MGI PMID:19706426 10136 Alb albumin gene MP:0001860 liver inflammation IAGP N RGD:5509061 20191205 MGI PMID:25453901 10136 Alb albumin gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180719 MGI PMID:23549084 10136 Alb albumin gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20191205 MGI PMID:25453901 10136 Alb albumin gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180719 MGI PMID:23549084 10136 Alb albumin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:15282742 10136 Alb albumin gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180719 MGI PMID:21109326 10136 Alb albumin gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20240222 MGI PMID:37451670 10136 Alb albumin gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20180719 MGI PMID:19706426 10136 Alb albumin gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180719 MGI PMID:20935052 10136 Alb albumin gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20191205 MGI PMID:25453901 10136 Alb albumin gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20240222 MGI PMID:37451670 10136 Alb albumin gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180719 MGI PMID:21109326 10136 Alb albumin gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20180719 MGI PMID:19706426 10136 Alb albumin gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20180719 MGI PMID:23549084 10136 Alb albumin gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20180719 MGI PMID:21109326 10136 Alb albumin gene MP:0003326 liver failure IAGP N RGD:5509061 20191205 MGI PMID:25453901 10136 Alb albumin gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20181129 MGI PMID:27032374 10136 Alb albumin gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20240222 MGI PMID:37451670 10136 Alb albumin gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20180719 MGI PMID:17908794 10136 Alb albumin gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20191205 MGI PMID:25453901 10136 Alb albumin gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20191205 MGI PMID:25453901 10136 Alb albumin gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20210422 MGI PMID:32381628 10136 Alb albumin gene MP:0003926 decreased cellular glucose uptake IAGP N RGD:5509061 20180719 MGI PMID:23549084 10136 Alb albumin gene MP:0004025 polyploidy IAGP N RGD:5509061 20221229 MGI PMID:29967292 10136 Alb albumin gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20191205 MGI PMID:25453901 10136 Alb albumin gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20180719 MGI PMID:17908794 10136 Alb albumin gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20180719 MGI PMID:23549084 10136 Alb albumin gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20191205 MGI PMID:25453901 10136 Alb albumin gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20180719 MGI PMID:21109326 10136 Alb albumin gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20240222 MGI PMID:37451670 10136 Alb albumin gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240222 MGI PMID:37451670 10136 Alb albumin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180719 MGI PMID:23549084 10136 Alb albumin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20220825 MGI PMID:33641163 10136 Alb albumin gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20191205 MGI PMID:25453901 10136 Alb albumin gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20180719 MGI PMID:17908794 10136 Alb albumin gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20180719 MGI 10136 Alb albumin gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20180719 MGI PMID:23549084 10136 Alb albumin gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20180719 MGI PMID:26921005 10136 Alb albumin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20220825 MGI PMID:33641163 10136 Alb albumin gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20180719 MGI PMID:19706426 10136 Alb albumin gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20240222 MGI PMID:37451670 10136 Alb albumin gene MP:0008738 abnormal liver iron level IAGP N RGD:5509061 20180719 MGI PMID:19492434 10136 Alb albumin gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20180719 MGI PMID:19706426 10136 Alb albumin gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20180719 MGI PMID:21109326 10136 Alb albumin gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20180719 MGI PMID:19706426 10136 Alb albumin gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180719 MGI PMID:21109326 10136 Alb albumin gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20180719 MGI PMID:23549084 10136 Alb albumin gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20240222 MGI PMID:37451670 10136 Alb albumin gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20180719 MGI PMID:21109326 10136 Alb albumin gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20180719 MGI PMID:23549084 10136 Alb albumin gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20240222 MGI PMID:37451670 10136 Alb albumin gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20180719 MGI PMID:20935052 10136 Alb albumin gene MP:0010297 increased hepatobiliary system tumor incidence IAGP N RGD:5509061 20180719 MGI PMID:26699479 10136 Alb albumin gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20180719 MGI PMID:23023701 10136 Alb albumin gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20181129 MGI PMID:27032374 10136 Alb albumin gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20220825 MGI PMID:33641163 10136 Alb albumin gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20180719 MGI PMID:21109326 10136 Alb albumin gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20180719 MGI PMID:23549084 10136 Alb albumin gene MP:0011435 increased urine magnesium level IAGP N RGD:5509061 20180719 MGI PMID:19706426 10136 Alb albumin gene MP:0011537 uraturia IAGP N RGD:5509061 20180719 MGI PMID:19706426 10136 Alb albumin gene MP:0011584 increased alkaline phosphatase activity IEA N RGD:5509061 20180719 MGI 10136 Alb albumin gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20240222 MGI PMID:37451670 10136 Alb albumin gene MP:0014476 abnormal feces lipid level IAGP N RGD:5509061 20240704 MGI PMID:17908794 10136 Alb albumin gene MP:0014478 increased feces bile salt level IAGP N RGD:5509061 20240704 MGI PMID:17908794 10136 Alb albumin gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20210422 MGI PMID:32381628 10136 Alb albumin gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20221229 MGI PMID:29967292 10136 Alb albumin gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20240118 MGI PMID:36638184 10136 Alb albumin gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20240118 MGI PMID:36638184 10136 Alb albumin gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20240118 MGI PMID:36638184 10136 Alb albumin gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20240118 MGI PMID:36638184 10136 Alb albumin gene MP:0030974 enhanced gluconeogenesis IAGP N RGD:5509061 20220825 MGI PMID:33641163 10136 Alb albumin gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240222 MGI PMID:37451670 10136 Alb albumin gene MP:0031601 decreased endoplasmic reticulum stress IAGP N RGD:5509061 20240418 MGI PMID:37451670 10136 Alb albumin gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:23549084 10139 Aldoa aldolase A, fructose-bisphosphate gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20200402 MGI 10139 Aldoa aldolase A, fructose-bisphosphate gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10139 Aldoa aldolase A, fructose-bisphosphate gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 10139 Aldoa aldolase A, fructose-bisphosphate gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 10140 Aldob aldolase B, fructose-bisphosphate gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20190502 MGI 10140 Aldob aldolase B, fructose-bisphosphate gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20151112 MGI PMID:25637246 10140 Aldob aldolase B, fructose-bisphosphate gene MP:0000603 pale liver IAGP N RGD:5509061 20151112 MGI PMID:25637246 10140 Aldob aldolase B, fructose-bisphosphate gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 10140 Aldob aldolase B, fructose-bisphosphate gene MP:0001265 decreased body size IAGP N RGD:5509061 20151112 MGI PMID:25637246 10140 Aldob aldolase B, fructose-bisphosphate gene MP:0001860 liver inflammation IAGP N RGD:5509061 20151112 MGI PMID:25637246 10140 Aldob aldolase B, fructose-bisphosphate gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20151112 MGI PMID:25637246 10140 Aldob aldolase B, fructose-bisphosphate gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20151112 MGI PMID:25637246 10140 Aldob aldolase B, fructose-bisphosphate gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20211021 MGI 10140 Aldob aldolase B, fructose-bisphosphate gene MP:0008993 abnormal portal triad morphology IAGP N RGD:5509061 20151112 MGI PMID:25637246 10140 Aldob aldolase B, fructose-bisphosphate gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20151112 MGI PMID:25637246 10140 Aldob aldolase B, fructose-bisphosphate gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 10143 Aldoc aldolase C, fructose-bisphosphate gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20240425 MGI PMID:38417553 10143 Aldoc aldolase C, fructose-bisphosphate gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20240425 MGI PMID:38417553 10143 Aldoc aldolase C, fructose-bisphosphate gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240425 MGI PMID:38417553 10143 Aldoc aldolase C, fructose-bisphosphate gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 10143 Aldoc aldolase C, fructose-bisphosphate gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20240425 MGI PMID:38417553 10143 Aldoc aldolase C, fructose-bisphosphate gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170105 MGI 10143 Aldoc aldolase C, fructose-bisphosphate gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150416 MGI PMID:24475166 10143 Aldoc aldolase C, fructose-bisphosphate gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20240425 MGI PMID:38417553 10143 Aldoc aldolase C, fructose-bisphosphate gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20240425 MGI PMID:38417553 10143 Aldoc aldolase C, fructose-bisphosphate gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 10143 Aldoc aldolase C, fructose-bisphosphate gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20240425 MGI PMID:38417553 10143 Aldoc aldolase C, fructose-bisphosphate gene MP:0005573 increased pulmonary respiratory rate IEA N RGD:5509061 20201022 MGI 10143 Aldoc aldolase C, fructose-bisphosphate gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 10143 Aldoc aldolase C, fructose-bisphosphate gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20240425 MGI PMID:38417553 10143 Aldoc aldolase C, fructose-bisphosphate gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20240425 MGI PMID:38417553 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16200066 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:7969451 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:7969451 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:7809134 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11867678 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:7969451 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:7809134 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0004822 decreased susceptibility to experimental autoimmune uveoretinitis IAGP N RGD:5509061 20141003 MGI PMID:16565390 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:7809134 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16200066 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:7809134 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16200066 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:7809134 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:7809134 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16200066 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:7809134 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0009817 decreased leukotriene level IAGP N RGD:5509061 20141003 MGI PMID:7809134 10147 Alox5 arachidonate 5-lipoxygenase gene MP:0009818 abnormal thromboxane level IAGP N RGD:5509061 20141003 MGI PMID:7809134 10148 Akp3 alkaline phosphatase 3, intestine, not Mn requiring gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:14560000 10148 Akp3 alkaline phosphatase 3, intestine, not Mn requiring gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:14560000 10148 Akp3 alkaline phosphatase 3, intestine, not Mn requiring gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14560000 10148 Akp3 alkaline phosphatase 3, intestine, not Mn requiring gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:14560000 10149 Ambn ameloblastin gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:15583034 10149 Ambn ameloblastin gene MP:0001297 microphthalmia IEA N RGD:5509061 20201022 MGI 10149 Ambn ameloblastin gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15583034 10149 Ambn ameloblastin gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 10149 Ambn ameloblastin gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20201022 MGI 10149 Ambn ameloblastin gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:15583034 10149 Ambn ameloblastin gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 10149 Ambn ameloblastin gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:15583034 10149 Ambn ameloblastin gene MP:0002989 small kidney IEA N RGD:5509061 20201022 MGI 10149 Ambn ameloblastin gene MP:0003068 enlarged kidney IEA N RGD:5509061 20201022 MGI 10149 Ambn ameloblastin gene MP:0003404 absent enamel IAGP N RGD:5509061 20141003 MGI PMID:15583034 10149 Ambn ameloblastin gene MP:0003932 abnormal molar crown morphology IAGP N RGD:5509061 20141003 MGI PMID:15583034 10149 Ambn ameloblastin gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:15583034 10149 Ambn ameloblastin gene MP:0010096 abnormal incisor color IAGP N RGD:5509061 20171005 MGI PMID:15583034 10149 Ambn ameloblastin gene MP:0030459 abnormal tooth attrition IAGP N RGD:5509061 20171221 MGI PMID:15583034 10150 Ambp alpha 1 microglobulin/bikunin precursor gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:11145954 10150 Ambp alpha 1 microglobulin/bikunin precursor gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11145954 10150 Ambp alpha 1 microglobulin/bikunin precursor gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11243855 10150 Ambp alpha 1 microglobulin/bikunin precursor gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:11145954 10150 Ambp alpha 1 microglobulin/bikunin precursor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11145954 10150 Ambp alpha 1 microglobulin/bikunin precursor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11243855 10150 Ambp alpha 1 microglobulin/bikunin precursor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11145954 10150 Ambp alpha 1 microglobulin/bikunin precursor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11243855 10150 Ambp alpha 1 microglobulin/bikunin precursor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11145954 10150 Ambp alpha 1 microglobulin/bikunin precursor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11243855 10150 Ambp alpha 1 microglobulin/bikunin precursor gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:11145954 10150 Ambp alpha 1 microglobulin/bikunin precursor gene MP:0003697 absent zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:11243855 10150 Ambp alpha 1 microglobulin/bikunin precursor gene MP:0009374 absent cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:11145954 10150 Ambp alpha 1 microglobulin/bikunin precursor gene MP:0009648 abnormal superovulation IAGP N RGD:5509061 20220630 MGI PMID:11243855 10151 Amd1 S-adenosylmethionine decarboxylase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11856372 10151 Amd1 S-adenosylmethionine decarboxylase 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11856372 10152 Amh anti-Mullerian hormone gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:7954809 10152 Amh anti-Mullerian hormone gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:7954809 10152 Amh anti-Mullerian hormone gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:7954809 10152 Amh anti-Mullerian hormone gene MP:0001749 suppressed circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10579345 10152 Amh anti-Mullerian hormone gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:7954809 10152 Amh anti-Mullerian hormone gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8895659 10152 Amh anti-Mullerian hormone gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:10571183 10152 Amh anti-Mullerian hormone gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:7954809 10152 Amh anti-Mullerian hormone gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:8895659 10152 Amh anti-Mullerian hormone gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:10571183 10152 Amh anti-Mullerian hormone gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:7954809 10152 Amh anti-Mullerian hormone gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:7954809 10152 Amh anti-Mullerian hormone gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:10571183 10152 Amh anti-Mullerian hormone gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:7954809 10152 Amh anti-Mullerian hormone gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:8895659 10152 Amh anti-Mullerian hormone gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:7954809 10152 Amh anti-Mullerian hormone gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:7954809 10152 Amh anti-Mullerian hormone gene MP:0004855 increased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:10579345 10152 Amh anti-Mullerian hormone gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8895659 10152 Amh anti-Mullerian hormone gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10579345 10152 Amh anti-Mullerian hormone gene MP:0011128 increased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10579345 10152 Amh anti-Mullerian hormone gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10579345 10154 Ampd1 adenosine monophosphate deaminase 1 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20181227 MGI 10154 Ampd1 adenosine monophosphate deaminase 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20160811 MGI 10154 Ampd1 adenosine monophosphate deaminase 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 10154 Ampd1 adenosine monophosphate deaminase 1 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20180621 MGI PMID:27896074 10154 Ampd1 adenosine monophosphate deaminase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20160421 MGI 10154 Ampd1 adenosine monophosphate deaminase 1 gene MP:0030604 abnormal ammonia homeostasis IAGP N RGD:5509061 20180628 MGI PMID:27896074 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20160804 MGI 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23078545 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23911318 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23911318 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23078545 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23542464 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:23911318 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23078545 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:23078545 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:23078545 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23078545 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:23911318 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:24066180 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:24066180 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:24066180 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23911318 10155 Ampd3 adenosine monophosphate deaminase 3 gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:23078545 10162 Anp32a acidic nuclear phosphoprotein 32 family member A gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21636789 10163 Slc25a5 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 5 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:14749836 10164 Anxa1 annexin A1 gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16835395 10164 Anxa1 annexin A1 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17405164 10164 Anxa1 annexin A1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17405164 10164 Anxa1 annexin A1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17405164 10164 Anxa1 annexin A1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17405164 10164 Anxa1 annexin A1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18802107 10164 Anxa1 annexin A1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:18802107 10164 Anxa1 annexin A1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0000692 small spleen IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18802107 10164 Anxa1 annexin A1 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:19805119 10164 Anxa1 annexin A1 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:21383699 10164 Anxa1 annexin A1 gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20141003 MGI PMID:17158208 10164 Anxa1 annexin A1 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:12475898 10164 Anxa1 annexin A1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12475898 10164 Anxa1 annexin A1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16835395 10164 Anxa1 annexin A1 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:12475898 10164 Anxa1 annexin A1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:19805119 10164 Anxa1 annexin A1 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:23241962 10164 Anxa1 annexin A1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:19805119 10164 Anxa1 annexin A1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21383699 10164 Anxa1 annexin A1 gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20160616 MGI PMID:19805119 10164 Anxa1 annexin A1 gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:17405164 10164 Anxa1 annexin A1 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19805119 10164 Anxa1 annexin A1 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20240523 MGI 10164 Anxa1 annexin A1 gene MP:0005129 increased adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:17026533 10164 Anxa1 annexin A1 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17405164 10164 Anxa1 annexin A1 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16835395 10164 Anxa1 annexin A1 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:16835395 10164 Anxa1 annexin A1 gene MP:0008302 thin adrenal cortex IAGP N RGD:5509061 20141003 MGI PMID:17158208 10164 Anxa1 annexin A1 gene MP:0008322 abnormal somatotroph morphology IAGP N RGD:5509061 20141003 MGI PMID:17026533 10164 Anxa1 annexin A1 gene MP:0008323 abnormal lactotroph morphology IAGP N RGD:5509061 20141003 MGI PMID:17026533 10164 Anxa1 annexin A1 gene MP:0008325 abnormal gonadotroph morphology IAGP N RGD:5509061 20141003 MGI PMID:17026533 10164 Anxa1 annexin A1 gene MP:0008327 abnormal corticotroph morphology IAGP N RGD:5509061 20141003 MGI PMID:17026533 10164 Anxa1 annexin A1 gene MP:0008427 decreased corticotroph cell size IAGP N RGD:5509061 20141003 MGI PMID:17026533 10164 Anxa1 annexin A1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:18802107 10164 Anxa1 annexin A1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19805119 10164 Anxa1 annexin A1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18802107 10164 Anxa1 annexin A1 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:19805119 10164 Anxa1 annexin A1 gene MP:0010935 increased airway resistance IEA N RGD:5509061 20230119 MGI 10164 Anxa1 annexin A1 gene MP:0013341 abnormal folliculo-stellate cell morphology IAGP N RGD:5509061 20141204 MGI PMID:17026533 10164 Anxa1 annexin A1 gene MP:0014166 ectopic cranial bone IAGP N RGD:5509061 20160407 MGI PMID:17405164 10164 Anxa1 annexin A1 gene MP:0020316 decreased vascular endothelial cell proliferation IAGP N RGD:5509061 20160616 MGI PMID:19805119 10166 Apc APC, WNT signaling pathway regulator gene MP:0000022 abnormal ear shape IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:20084116 10166 Apc APC, WNT signaling pathway regulator gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0000158 absent sternum IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:12584168 10166 Apc APC, WNT signaling pathway regulator gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:17942902 10166 Apc APC, WNT signaling pathway regulator gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20663863 10166 Apc APC, WNT signaling pathway regulator gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:2296722 10166 Apc APC, WNT signaling pathway regulator gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20141030 MGI PMID:18077429 10166 Apc APC, WNT signaling pathway regulator gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19147584 10166 Apc APC, WNT signaling pathway regulator gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19248780 10166 Apc APC, WNT signaling pathway regulator gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20181129 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20181129 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10783317 10166 Apc APC, WNT signaling pathway regulator gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17989230 10166 Apc APC, WNT signaling pathway regulator gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:12584168 10166 Apc APC, WNT signaling pathway regulator gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:8945508 10166 Apc APC, WNT signaling pathway regulator gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18829546 10166 Apc APC, WNT signaling pathway regulator gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20160128 MGI PMID:15716339 10166 Apc APC, WNT signaling pathway regulator gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20170608 MGI PMID:26527802 10166 Apc APC, WNT signaling pathway regulator gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:10783317 10166 Apc APC, WNT signaling pathway regulator gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:15731405 10166 Apc APC, WNT signaling pathway regulator gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18829546 10166 Apc APC, WNT signaling pathway regulator gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:15502862 10166 Apc APC, WNT signaling pathway regulator gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:17942902 10166 Apc APC, WNT signaling pathway regulator gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:20663863 10166 Apc APC, WNT signaling pathway regulator gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:14625550 10166 Apc APC, WNT signaling pathway regulator gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20160128 MGI PMID:15716339 10166 Apc APC, WNT signaling pathway regulator gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:14625550 10166 Apc APC, WNT signaling pathway regulator gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:15546883 10166 Apc APC, WNT signaling pathway regulator gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19011632 10166 Apc APC, WNT signaling pathway regulator gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:17332369 10166 Apc APC, WNT signaling pathway regulator gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141030 MGI PMID:15967128 10166 Apc APC, WNT signaling pathway regulator gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20818428 10166 Apc APC, WNT signaling pathway regulator gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:18264107 10166 Apc APC, WNT signaling pathway regulator gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:18264107 10166 Apc APC, WNT signaling pathway regulator gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:22251704 10166 Apc APC, WNT signaling pathway regulator gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:22251704 10166 Apc APC, WNT signaling pathway regulator gene MP:0000619 salivary gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:11215675 10166 Apc APC, WNT signaling pathway regulator gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8415640 10166 Apc APC, WNT signaling pathway regulator gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11215675 10166 Apc APC, WNT signaling pathway regulator gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16288217 10166 Apc APC, WNT signaling pathway regulator gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:16025118 10166 Apc APC, WNT signaling pathway regulator gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:20084116 10166 Apc APC, WNT signaling pathway regulator gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:21307168 10166 Apc APC, WNT signaling pathway regulator gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11215675 10166 Apc APC, WNT signaling pathway regulator gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11215675 10166 Apc APC, WNT signaling pathway regulator gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:11215675 10166 Apc APC, WNT signaling pathway regulator gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11215675 10166 Apc APC, WNT signaling pathway regulator gene MP:0001140 abnormal vagina epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11215675 10166 Apc APC, WNT signaling pathway regulator gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:17363566 10166 Apc APC, WNT signaling pathway regulator gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0001210 skin ridges IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11215675 10166 Apc APC, WNT signaling pathway regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15550389 10166 Apc APC, WNT signaling pathway regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17942902 10166 Apc APC, WNT signaling pathway regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20663863 10166 Apc APC, WNT signaling pathway regulator gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:12584168 10166 Apc APC, WNT signaling pathway regulator gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10346819 10166 Apc APC, WNT signaling pathway regulator gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:21251616 10166 Apc APC, WNT signaling pathway regulator gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22158121 10166 Apc APC, WNT signaling pathway regulator gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23955540 10166 Apc APC, WNT signaling pathway regulator gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20170615 MGI PMID:26411367 10166 Apc APC, WNT signaling pathway regulator gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20180125 MGI PMID:22452792 10166 Apc APC, WNT signaling pathway regulator gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:22009253 10166 Apc APC, WNT signaling pathway regulator gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:23955081 10166 Apc APC, WNT signaling pathway regulator gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:14522940 10166 Apc APC, WNT signaling pathway regulator gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:2296722 10166 Apc APC, WNT signaling pathway regulator gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14522940 10166 Apc APC, WNT signaling pathway regulator gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170615 MGI PMID:26411367 10166 Apc APC, WNT signaling pathway regulator gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:14522940 10166 Apc APC, WNT signaling pathway regulator gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:22251704 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10783317 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12584168 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15502862 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16288217 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17942902 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17989230 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18414679 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19248780 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20010873 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20176656 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20663863 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22009253 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:2296722 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20150611 MGI PMID:8674041 10166 Apc APC, WNT signaling pathway regulator gene MP:0001577 anemia IAGP N RGD:5509061 20180329 MGI PMID:26216032 10166 Apc APC, WNT signaling pathway regulator gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:22251704 10166 Apc APC, WNT signaling pathway regulator gene MP:0001661 extended life span IAGP N RGD:5509061 20160512 MGI PMID:1541640 10166 Apc APC, WNT signaling pathway regulator gene MP:0001661 extended life span IAGP N RGD:5509061 20191107 MGI PMID:30224759 10166 Apc APC, WNT signaling pathway regulator gene MP:0001661 extended life span IAGP N RGD:5509061 20211125 MGI PMID:30374053 10166 Apc APC, WNT signaling pathway regulator gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:18171987 10166 Apc APC, WNT signaling pathway regulator gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:7496034 10166 Apc APC, WNT signaling pathway regulator gene MP:0001697 abnormal embryo size IAGP N RGD:5509061 20141003 MGI PMID:7496034 10166 Apc APC, WNT signaling pathway regulator gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7496034 10166 Apc APC, WNT signaling pathway regulator gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10346819 10166 Apc APC, WNT signaling pathway regulator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12941845 10166 Apc APC, WNT signaling pathway regulator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17942902 10166 Apc APC, WNT signaling pathway regulator gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16025118 10166 Apc APC, WNT signaling pathway regulator gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16025118 10166 Apc APC, WNT signaling pathway regulator gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:22251704 10166 Apc APC, WNT signaling pathway regulator gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10783317 10166 Apc APC, WNT signaling pathway regulator gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15502862 10166 Apc APC, WNT signaling pathway regulator gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17942902 10166 Apc APC, WNT signaling pathway regulator gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19578404 10166 Apc APC, WNT signaling pathway regulator gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23955540 10166 Apc APC, WNT signaling pathway regulator gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20151008 MGI PMID:23551873 10166 Apc APC, WNT signaling pathway regulator gene MP:0002013 increased pilomatricoma incidence IAGP N RGD:5509061 20151008 MGI PMID:23551873 10166 Apc APC, WNT signaling pathway regulator gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:24474556 10166 Apc APC, WNT signaling pathway regulator gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12119409 10166 Apc APC, WNT signaling pathway regulator gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18056981 10166 Apc APC, WNT signaling pathway regulator gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23764754 10166 Apc APC, WNT signaling pathway regulator gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 10166 Apc APC, WNT signaling pathway regulator gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10992298 10166 Apc APC, WNT signaling pathway regulator gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12584168 10166 Apc APC, WNT signaling pathway regulator gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17363566 10166 Apc APC, WNT signaling pathway regulator gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17942902 10166 Apc APC, WNT signaling pathway regulator gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19578404 10166 Apc APC, WNT signaling pathway regulator gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9037065 10166 Apc APC, WNT signaling pathway regulator gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:11215675 10166 Apc APC, WNT signaling pathway regulator gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 10166 Apc APC, WNT signaling pathway regulator gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12584168 10166 Apc APC, WNT signaling pathway regulator gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17332369 10166 Apc APC, WNT signaling pathway regulator gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20080688 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12242442 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15502862 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15650110 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15703196 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15731405 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17332369 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18264107 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18562324 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20010873 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20080688 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20197623 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20886217 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9311916 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20151112 MGI PMID:25053805 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20180329 MGI PMID:26216032 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20200820 MGI PMID:32728212 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20210225 MGI PMID:30952657 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20220217 MGI PMID:34934045 10166 Apc APC, WNT signaling pathway regulator gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20240718 MGI PMID:35605119 10166 Apc APC, WNT signaling pathway regulator gene MP:0002045 increased renal cystadenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15550389 10166 Apc APC, WNT signaling pathway regulator gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10987272 10166 Apc APC, WNT signaling pathway regulator gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11731407 10166 Apc APC, WNT signaling pathway regulator gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11779834 10166 Apc APC, WNT signaling pathway regulator gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12730693 10166 Apc APC, WNT signaling pathway regulator gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14534534 10166 Apc APC, WNT signaling pathway regulator gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15366372 10166 Apc APC, WNT signaling pathway regulator gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15958588 10166 Apc APC, WNT signaling pathway regulator gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16581773 10166 Apc APC, WNT signaling pathway regulator gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17909008 10166 Apc APC, WNT signaling pathway regulator gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18414679 10166 Apc APC, WNT signaling pathway regulator gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19002110 10166 Apc APC, WNT signaling pathway regulator gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19690388 10166 Apc APC, WNT signaling pathway regulator gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20084116 10166 Apc APC, WNT signaling pathway regulator gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20190912 MGI PMID:29844172 10166 Apc APC, WNT signaling pathway regulator gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:19170756 10166 Apc APC, WNT signaling pathway regulator gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:19574546 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10096563 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10783317 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10987272 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10992298 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11773073 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12119409 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12130785 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12584168 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12730693 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15502862 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15550389 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15563600 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16288217 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16354691 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17363566 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17942902 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17989230 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18171987 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18264107 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18372904 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19011632 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19168705 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19248780 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19578404 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20010873 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20176656 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20663863 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22251704 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:2296722 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23318432 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24667635 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8090754 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9443401 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9506519 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9515784 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9617344 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20150611 MGI PMID:8674041 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20151008 MGI PMID:23551873 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20151112 MGI PMID:25053805 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20160128 MGI PMID:15716339 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20160512 MGI PMID:1541640 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20170615 MGI PMID:26411367 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20180329 MGI PMID:26216032 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20210211 MGI PMID:31662330 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20210225 MGI PMID:30952657 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20220217 MGI PMID:34934045 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20240111 MGI PMID:37459052 10166 Apc APC, WNT signaling pathway regulator gene MP:0002083 premature death IAGP N RGD:5509061 20240718 MGI PMID:35605119 10166 Apc APC, WNT signaling pathway regulator gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16025118 10166 Apc APC, WNT signaling pathway regulator gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:11130972 10166 Apc APC, WNT signaling pathway regulator gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20180329 MGI PMID:26216032 10166 Apc APC, WNT signaling pathway regulator gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20210701 MGI PMID:33879799 10166 Apc APC, WNT signaling pathway regulator gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18171987 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10489374 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11756685 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12130785 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12183406 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12242442 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12384562 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12584168 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12941845 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15456865 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15502862 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15731405 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16204028 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16288217 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16354691 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17283118 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17989230 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18056424 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18829546 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19168705 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19248780 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19574546 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20010873 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20176656 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20197623 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20531296 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20663863 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20886217 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21383188 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22009253 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22464327 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:2296722 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23075849 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23741059 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23955081 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24204315 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7753829 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8090754 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9126737 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9515784 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9617344 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141030 MGI PMID:15967128 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20150326 MGI PMID:23318432 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20150611 MGI PMID:8674041 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20151126 MGI PMID:23773267 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20160512 MGI PMID:1541640 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20160512 MGI PMID:15650110 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20170608 MGI PMID:26527802 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20180215 MGI PMID:27562646 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20180329 MGI PMID:26216032 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20190912 MGI PMID:29844172 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20200820 MGI PMID:32728212 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20210211 MGI PMID:31662330 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20210617 MGI PMID:33188295 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20240606 MGI PMID:31239271 10166 Apc APC, WNT signaling pathway regulator gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20240718 MGI PMID:35605119 10166 Apc APC, WNT signaling pathway regulator gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18504307 10166 Apc APC, WNT signaling pathway regulator gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:22251704 10166 Apc APC, WNT signaling pathway regulator gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:14522940 10166 Apc APC, WNT signaling pathway regulator gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0002732 increased trichoepithelioma incidence IAGP N RGD:5509061 20151008 MGI PMID:23551873 10166 Apc APC, WNT signaling pathway regulator gene MP:0002816 colitis IAGP N RGD:5509061 20150618 MGI PMID:17332369 10166 Apc APC, WNT signaling pathway regulator gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11040191 10166 Apc APC, WNT signaling pathway regulator gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15033975 10166 Apc APC, WNT signaling pathway regulator gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15502862 10166 Apc APC, WNT signaling pathway regulator gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16288217 10166 Apc APC, WNT signaling pathway regulator gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18372904 10166 Apc APC, WNT signaling pathway regulator gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18719115 10166 Apc APC, WNT signaling pathway regulator gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19011632 10166 Apc APC, WNT signaling pathway regulator gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19147584 10166 Apc APC, WNT signaling pathway regulator gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20176656 10166 Apc APC, WNT signaling pathway regulator gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22158121 10166 Apc APC, WNT signaling pathway regulator gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:2296722 10166 Apc APC, WNT signaling pathway regulator gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7954427 10166 Apc APC, WNT signaling pathway regulator gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8090754 10166 Apc APC, WNT signaling pathway regulator gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9506519 10166 Apc APC, WNT signaling pathway regulator gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20180329 MGI PMID:26216032 10166 Apc APC, WNT signaling pathway regulator gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:15550389 10166 Apc APC, WNT signaling pathway regulator gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:7496034 10166 Apc APC, WNT signaling pathway regulator gene MP:0003104 acrania IAGP N RGD:5509061 20141003 MGI PMID:20084116 10166 Apc APC, WNT signaling pathway regulator gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:10783317 10166 Apc APC, WNT signaling pathway regulator gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:11756685 10166 Apc APC, WNT signaling pathway regulator gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:14625550 10166 Apc APC, WNT signaling pathway regulator gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:15650110 10166 Apc APC, WNT signaling pathway regulator gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:16288217 10166 Apc APC, WNT signaling pathway regulator gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:18504307 10166 Apc APC, WNT signaling pathway regulator gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:18719115 10166 Apc APC, WNT signaling pathway regulator gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:20197623 10166 Apc APC, WNT signaling pathway regulator gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:20663863 10166 Apc APC, WNT signaling pathway regulator gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:21996741 10166 Apc APC, WNT signaling pathway regulator gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:8945508 10166 Apc APC, WNT signaling pathway regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:17942902 10166 Apc APC, WNT signaling pathway regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:17989230 10166 Apc APC, WNT signaling pathway regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:20176656 10166 Apc APC, WNT signaling pathway regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20150611 MGI PMID:8674041 10166 Apc APC, WNT signaling pathway regulator gene MP:0003272 duodenal atresia IAGP N RGD:5509061 20170615 MGI PMID:26411367 10166 Apc APC, WNT signaling pathway regulator gene MP:0003292 melena IAGP N RGD:5509061 20141003 MGI PMID:10096563 10166 Apc APC, WNT signaling pathway regulator gene MP:0003292 melena IAGP N RGD:5509061 20141003 MGI PMID:2296722 10166 Apc APC, WNT signaling pathway regulator gene MP:0003292 melena IAGP N RGD:5509061 20240530 MGI PMID:20663863 10166 Apc APC, WNT signaling pathway regulator gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15502862 10166 Apc APC, WNT signaling pathway regulator gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8090754 10166 Apc APC, WNT signaling pathway regulator gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:15650110 10166 Apc APC, WNT signaling pathway regulator gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:16288217 10166 Apc APC, WNT signaling pathway regulator gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:21996741 10166 Apc APC, WNT signaling pathway regulator gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:19011632 10166 Apc APC, WNT signaling pathway regulator gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15563600 10166 Apc APC, WNT signaling pathway regulator gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20084116 10166 Apc APC, WNT signaling pathway regulator gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8090754 10166 Apc APC, WNT signaling pathway regulator gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:19578404 10166 Apc APC, WNT signaling pathway regulator gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:9506519 10166 Apc APC, WNT signaling pathway regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:11731407 10166 Apc APC, WNT signaling pathway regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:12730693 10166 Apc APC, WNT signaling pathway regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:16354691 10166 Apc APC, WNT signaling pathway regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:19002110 10166 Apc APC, WNT signaling pathway regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20886217 10166 Apc APC, WNT signaling pathway regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21467224 10166 Apc APC, WNT signaling pathway regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23034650 10166 Apc APC, WNT signaling pathway regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23726973 10166 Apc APC, WNT signaling pathway regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23741059 10166 Apc APC, WNT signaling pathway regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20170413 MGI PMID:19893577 10166 Apc APC, WNT signaling pathway regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20170608 MGI PMID:26527802 10166 Apc APC, WNT signaling pathway regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20190912 MGI PMID:29844172 10166 Apc APC, WNT signaling pathway regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20210617 MGI PMID:33658388 10166 Apc APC, WNT signaling pathway regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20210701 MGI PMID:33879799 10166 Apc APC, WNT signaling pathway regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20211125 MGI PMID:30374053 10166 Apc APC, WNT signaling pathway regulator gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:18829546 10166 Apc APC, WNT signaling pathway regulator gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:19248780 10166 Apc APC, WNT signaling pathway regulator gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:23202126 10166 Apc APC, WNT signaling pathway regulator gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:9037065 10166 Apc APC, WNT signaling pathway regulator gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17332369 10166 Apc APC, WNT signaling pathway regulator gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20160128 MGI PMID:15716339 10166 Apc APC, WNT signaling pathway regulator gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20141003 MGI PMID:24474556 10166 Apc APC, WNT signaling pathway regulator gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20160714 MGI PMID:17418409 10166 Apc APC, WNT signaling pathway regulator gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:15550389 10166 Apc APC, WNT signaling pathway regulator gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:14625550 10166 Apc APC, WNT signaling pathway regulator gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:15703196 10166 Apc APC, WNT signaling pathway regulator gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:18056424 10166 Apc APC, WNT signaling pathway regulator gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20010873 10166 Apc APC, WNT signaling pathway regulator gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20852630 10166 Apc APC, WNT signaling pathway regulator gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20886217 10166 Apc APC, WNT signaling pathway regulator gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23075849 10166 Apc APC, WNT signaling pathway regulator gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20210617 MGI PMID:33188295 10166 Apc APC, WNT signaling pathway regulator gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20151008 MGI PMID:23551873 10166 Apc APC, WNT signaling pathway regulator gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:12941845 10166 Apc APC, WNT signaling pathway regulator gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22251704 10166 Apc APC, WNT signaling pathway regulator gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20170615 MGI PMID:26411367 10166 Apc APC, WNT signaling pathway regulator gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:23741059 10166 Apc APC, WNT signaling pathway regulator gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:7954427 10166 Apc APC, WNT signaling pathway regulator gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:14625550 10166 Apc APC, WNT signaling pathway regulator gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0004344 scapular bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11215675 10166 Apc APC, WNT signaling pathway regulator gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:20084116 10166 Apc APC, WNT signaling pathway regulator gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:20663863 10166 Apc APC, WNT signaling pathway regulator gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:8415640 10166 Apc APC, WNT signaling pathway regulator gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:12750251 10166 Apc APC, WNT signaling pathway regulator gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11130972 10166 Apc APC, WNT signaling pathway regulator gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20210617 MGI PMID:33658388 10166 Apc APC, WNT signaling pathway regulator gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0004713 split notochord IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0004733 abnormal thoracic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0004790 absent upper incisors IAGP N RGD:5509061 20170803 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:11215675 10166 Apc APC, WNT signaling pathway regulator gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20160128 MGI PMID:15716339 10166 Apc APC, WNT signaling pathway regulator gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17332369 10166 Apc APC, WNT signaling pathway regulator gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0004894 uterus atrophy IAGP N RGD:5509061 20141003 MGI PMID:11215675 10166 Apc APC, WNT signaling pathway regulator gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20084116 10166 Apc APC, WNT signaling pathway regulator gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16025118 10166 Apc APC, WNT signaling pathway regulator gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15563600 10166 Apc APC, WNT signaling pathway regulator gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:18414679 10166 Apc APC, WNT signaling pathway regulator gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:23955081 10166 Apc APC, WNT signaling pathway regulator gene MP:0005150 cachexia IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14522940 10166 Apc APC, WNT signaling pathway regulator gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20170615 MGI PMID:26411367 10166 Apc APC, WNT signaling pathway regulator gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:7478622 10166 Apc APC, WNT signaling pathway regulator gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:15550389 10166 Apc APC, WNT signaling pathway regulator gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12119409 10166 Apc APC, WNT signaling pathway regulator gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12417741 10166 Apc APC, WNT signaling pathway regulator gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15650110 10166 Apc APC, WNT signaling pathway regulator gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22344573 10166 Apc APC, WNT signaling pathway regulator gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14625550 10166 Apc APC, WNT signaling pathway regulator gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19248780 10166 Apc APC, WNT signaling pathway regulator gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23955081 10166 Apc APC, WNT signaling pathway regulator gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14625550 10166 Apc APC, WNT signaling pathway regulator gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0006401 absent male preputial gland IAGP N RGD:5509061 20141003 MGI PMID:10346819 10166 Apc APC, WNT signaling pathway regulator gene MP:0006422 increased mammary adenoacanthoma incidence IAGP N RGD:5509061 20150219 MGI PMID:10489374 10166 Apc APC, WNT signaling pathway regulator gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24474556 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:10987272 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:11274413 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:11756685 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:11888894 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:12384562 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:14522940 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:15033975 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:16204028 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:16288217 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:17989230 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:18171987 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:18264107 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:18504307 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:18829546 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:19168705 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:19690388 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:20084116 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:20886217 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:21996741 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:23118011 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:23202126 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:9515784 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141030 MGI PMID:18077429 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20150611 MGI PMID:23741483 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20151112 MGI PMID:25053805 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20180329 MGI PMID:26216032 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20190912 MGI PMID:29844172 10166 Apc APC, WNT signaling pathway regulator gene MP:0008011 intestine polyps IAGP N RGD:5509061 20211021 MGI PMID:34489406 10166 Apc APC, WNT signaling pathway regulator gene MP:0008012 duodenum polyps IAGP N RGD:5509061 20160616 MGI PMID:25578479 10166 Apc APC, WNT signaling pathway regulator gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19578404 10166 Apc APC, WNT signaling pathway regulator gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:22251704 10166 Apc APC, WNT signaling pathway regulator gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:22251704 10166 Apc APC, WNT signaling pathway regulator gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22251704 10166 Apc APC, WNT signaling pathway regulator gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:20084116 10166 Apc APC, WNT signaling pathway regulator gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:12130785 10166 Apc APC, WNT signaling pathway regulator gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20200618 MGI PMID:18504307 10166 Apc APC, WNT signaling pathway regulator gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18504307 10166 Apc APC, WNT signaling pathway regulator gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:15550389 10166 Apc APC, WNT signaling pathway regulator gene MP:0008533 abnormal anterior visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141030 MGI PMID:18077429 10166 Apc APC, WNT signaling pathway regulator gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22251704 10166 Apc APC, WNT signaling pathway regulator gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22251704 10166 Apc APC, WNT signaling pathway regulator gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20210617 MGI PMID:33753942 10166 Apc APC, WNT signaling pathway regulator gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:22251704 10166 Apc APC, WNT signaling pathway regulator gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20190912 MGI PMID:29844172 10166 Apc APC, WNT signaling pathway regulator gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20170615 MGI PMID:26411367 10166 Apc APC, WNT signaling pathway regulator gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:22251704 10166 Apc APC, WNT signaling pathway regulator gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20190912 MGI PMID:29844172 10166 Apc APC, WNT signaling pathway regulator gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0008780 increased pancreatic acinar cell carcinoma incidence IAGP N RGD:5509061 20150326 MGI PMID:7478622 10166 Apc APC, WNT signaling pathway regulator gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18483247 10166 Apc APC, WNT signaling pathway regulator gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20160128 MGI PMID:15716339 10166 Apc APC, WNT signaling pathway regulator gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20180125 MGI PMID:22452792 10166 Apc APC, WNT signaling pathway regulator gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20170413 MGI PMID:19893577 10166 Apc APC, WNT signaling pathway regulator gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:18056424 10166 Apc APC, WNT signaling pathway regulator gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17332369 10166 Apc APC, WNT signaling pathway regulator gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21996741 10166 Apc APC, WNT signaling pathway regulator gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23318432 10166 Apc APC, WNT signaling pathway regulator gene MP:0009078 adrenal gland hyperplasia IAGP N RGD:5509061 20141120 MGI PMID:11215675 10166 Apc APC, WNT signaling pathway regulator gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:24474556 10166 Apc APC, WNT signaling pathway regulator gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20170615 MGI PMID:26411367 10166 Apc APC, WNT signaling pathway regulator gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9506519 10166 Apc APC, WNT signaling pathway regulator gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200423 MGI PMID:30858608 10166 Apc APC, WNT signaling pathway regulator gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20170615 MGI PMID:26411367 10166 Apc APC, WNT signaling pathway regulator gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20170615 MGI PMID:26411367 10166 Apc APC, WNT signaling pathway regulator gene MP:0009209 abnormal internal female genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:24474556 10166 Apc APC, WNT signaling pathway regulator gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:17363566 10166 Apc APC, WNT signaling pathway regulator gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17363566 10166 Apc APC, WNT signaling pathway regulator gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 10166 Apc APC, WNT signaling pathway regulator gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20080688 10166 Apc APC, WNT signaling pathway regulator gene MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17909008 10166 Apc APC, WNT signaling pathway regulator gene MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17942902 10166 Apc APC, WNT signaling pathway regulator gene MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20176656 10166 Apc APC, WNT signaling pathway regulator gene MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21251616 10166 Apc APC, WNT signaling pathway regulator gene MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20180329 MGI PMID:26216032 10166 Apc APC, WNT signaling pathway regulator gene MP:0009310 increased large intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20176656 10166 Apc APC, WNT signaling pathway regulator gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21251616 10166 Apc APC, WNT signaling pathway regulator gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20151112 MGI PMID:25053805 10166 Apc APC, WNT signaling pathway regulator gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20180329 MGI PMID:26216032 10166 Apc APC, WNT signaling pathway regulator gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:20084116 10166 Apc APC, WNT signaling pathway regulator gene MP:0009539 abnormal Hassall's corpuscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:2296722 10166 Apc APC, WNT signaling pathway regulator gene MP:0009733 absent nipple IAGP N RGD:5509061 20141003 MGI PMID:11215675 10166 Apc APC, WNT signaling pathway regulator gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23726973 10166 Apc APC, WNT signaling pathway regulator gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:12941845 10166 Apc APC, WNT signaling pathway regulator gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:10987272 10166 Apc APC, WNT signaling pathway regulator gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20170608 MGI PMID:26527802 10166 Apc APC, WNT signaling pathway regulator gene MP:0009850 embryonic lethality between implantation and placentation IAGP N RGD:5509061 20141003 MGI PMID:7496034 10166 Apc APC, WNT signaling pathway regulator gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20170413 MGI PMID:19893577 10166 Apc APC, WNT signaling pathway regulator gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20190912 MGI PMID:29844172 10166 Apc APC, WNT signaling pathway regulator gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0010156 abnormal small intestinal crypt cell physiology IAGP N RGD:5509061 20170608 MGI PMID:26527802 10166 Apc APC, WNT signaling pathway regulator gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20160128 MGI PMID:15716339 10166 Apc APC, WNT signaling pathway regulator gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20170615 MGI PMID:26411367 10166 Apc APC, WNT signaling pathway regulator gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11130972 10166 Apc APC, WNT signaling pathway regulator gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18056448 10166 Apc APC, WNT signaling pathway regulator gene MP:0010273 increased classified tumor incidence IAGP N RGD:5509061 20180329 MGI PMID:26216032 10166 Apc APC, WNT signaling pathway regulator gene MP:0010274 increased organ/body region tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20080688 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10783317 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11773073 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11865977 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12119409 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12242442 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12417741 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17332369 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17942902 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18414679 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19147584 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19578404 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20176656 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20852630 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21307168 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22158121 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23034650 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24204315 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20151112 MGI PMID:25053805 10166 Apc APC, WNT signaling pathway regulator gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20220721 MGI PMID:35673579 10166 Apc APC, WNT signaling pathway regulator gene MP:0010287 increased reproductive system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24474556 10166 Apc APC, WNT signaling pathway regulator gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10783317 10166 Apc APC, WNT signaling pathway regulator gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11215675 10166 Apc APC, WNT signaling pathway regulator gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19578404 10166 Apc APC, WNT signaling pathway regulator gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8415640 10166 Apc APC, WNT signaling pathway regulator gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20151008 MGI PMID:23551873 10166 Apc APC, WNT signaling pathway regulator gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 10166 Apc APC, WNT signaling pathway regulator gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20151008 MGI PMID:23551873 10166 Apc APC, WNT signaling pathway regulator gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10783317 10166 Apc APC, WNT signaling pathway regulator gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11040191 10166 Apc APC, WNT signaling pathway regulator gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19578404 10166 Apc APC, WNT signaling pathway regulator gene MP:0010313 increased osteoma incidence IAGP N RGD:5509061 20151008 MGI PMID:23551873 10166 Apc APC, WNT signaling pathway regulator gene MP:0010318 increased salivary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10489374 10166 Apc APC, WNT signaling pathway regulator gene MP:0010338 increased desmoid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19578404 10166 Apc APC, WNT signaling pathway regulator gene MP:0010338 increased desmoid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20176656 10166 Apc APC, WNT signaling pathway regulator gene MP:0010352 gastrointestinal tract polyps IAGP N RGD:5509061 20141003 MGI PMID:19248780 10166 Apc APC, WNT signaling pathway regulator gene MP:0010352 gastrointestinal tract polyps IAGP N RGD:5509061 20141003 MGI PMID:22009253 10166 Apc APC, WNT signaling pathway regulator gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 10166 Apc APC, WNT signaling pathway regulator gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15703196 10166 Apc APC, WNT signaling pathway regulator gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18719115 10166 Apc APC, WNT signaling pathway regulator gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22009253 10166 Apc APC, WNT signaling pathway regulator gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20141003 MGI PMID:22009253 10166 Apc APC, WNT signaling pathway regulator gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20170413 MGI PMID:19893577 10166 Apc APC, WNT signaling pathway regulator gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20211125 MGI PMID:30374053 10166 Apc APC, WNT signaling pathway regulator gene MP:0010681 abnormal hair follicle bulb morphology IAGP N RGD:5509061 20181129 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0010769 abnormal survival IAGP N RGD:5509061 20170413 MGI PMID:19893577 10166 Apc APC, WNT signaling pathway regulator gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18264107 10166 Apc APC, WNT signaling pathway regulator gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19578404 10166 Apc APC, WNT signaling pathway regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10346819 10166 Apc APC, WNT signaling pathway regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15550389 10166 Apc APC, WNT signaling pathway regulator gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170615 MGI PMID:26411367 10166 Apc APC, WNT signaling pathway regulator gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20084116 10166 Apc APC, WNT signaling pathway regulator gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10783317 10166 Apc APC, WNT signaling pathway regulator gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15502862 10166 Apc APC, WNT signaling pathway regulator gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22009253 10166 Apc APC, WNT signaling pathway regulator gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17942902 10166 Apc APC, WNT signaling pathway regulator gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21307168 10166 Apc APC, WNT signaling pathway regulator gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7496034 10166 Apc APC, WNT signaling pathway regulator gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8090754 10166 Apc APC, WNT signaling pathway regulator gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20084116 10166 Apc APC, WNT signaling pathway regulator gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16204028 10166 Apc APC, WNT signaling pathway regulator gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20151008 MGI PMID:23551873 10166 Apc APC, WNT signaling pathway regulator gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17332369 10166 Apc APC, WNT signaling pathway regulator gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7753829 10166 Apc APC, WNT signaling pathway regulator gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20084116 10166 Apc APC, WNT signaling pathway regulator gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20170803 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20180329 MGI PMID:26216032 10166 Apc APC, WNT signaling pathway regulator gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:20084116 10166 Apc APC, WNT signaling pathway regulator gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:20084116 10166 Apc APC, WNT signaling pathway regulator gene MP:0012156 rostral-caudal axis duplication IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:21307168 10166 Apc APC, WNT signaling pathway regulator gene MP:0012165 absent neural folds IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0012176 abnormal head development IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24474556 10166 Apc APC, WNT signaling pathway regulator gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11130972 10166 Apc APC, WNT signaling pathway regulator gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21467224 10166 Apc APC, WNT signaling pathway regulator gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23075849 10166 Apc APC, WNT signaling pathway regulator gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23955081 10166 Apc APC, WNT signaling pathway regulator gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8242739 10166 Apc APC, WNT signaling pathway regulator gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20180215 MGI PMID:27562646 10166 Apc APC, WNT signaling pathway regulator gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20200820 MGI PMID:32728212 10166 Apc APC, WNT signaling pathway regulator gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20210701 MGI PMID:33879799 10166 Apc APC, WNT signaling pathway regulator gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20240718 MGI PMID:35605119 10166 Apc APC, WNT signaling pathway regulator gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 10166 Apc APC, WNT signaling pathway regulator gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18483247 10166 Apc APC, WNT signaling pathway regulator gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23318432 10166 Apc APC, WNT signaling pathway regulator gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23955081 10166 Apc APC, WNT signaling pathway regulator gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8242739 10166 Apc APC, WNT signaling pathway regulator gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20160512 MGI PMID:1541640 10166 Apc APC, WNT signaling pathway regulator gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20170413 MGI PMID:19893577 10166 Apc APC, WNT signaling pathway regulator gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20170608 MGI PMID:26527802 10166 Apc APC, WNT signaling pathway regulator gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20191107 MGI PMID:30224759 10166 Apc APC, WNT signaling pathway regulator gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20210701 MGI PMID:33879799 10166 Apc APC, WNT signaling pathway regulator gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20211125 MGI PMID:30374053 10166 Apc APC, WNT signaling pathway regulator gene MP:0012435 decreased colon tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23955081 10166 Apc APC, WNT signaling pathway regulator gene MP:0012435 decreased colon tumor incidence IAGP N RGD:5509061 20230302 MGI PMID:28583252 10166 Apc APC, WNT signaling pathway regulator gene MP:0012436 increased colon tumor incidence IAGP N RGD:5509061 20151112 MGI PMID:25053805 10166 Apc APC, WNT signaling pathway regulator gene MP:0012436 increased colon tumor incidence IAGP N RGD:5509061 20191205 MGI PMID:26731471 10166 Apc APC, WNT signaling pathway regulator gene MP:0012436 increased colon tumor incidence IAGP N RGD:5509061 20201119 MGI PMID:31296963 10166 Apc APC, WNT signaling pathway regulator gene MP:0012436 increased colon tumor incidence IAGP N RGD:5509061 20210211 MGI PMID:31662330 10166 Apc APC, WNT signaling pathway regulator gene MP:0012436 increased colon tumor incidence IAGP N RGD:5509061 20220120 MGI PMID:34615997 10166 Apc APC, WNT signaling pathway regulator gene MP:0012436 increased colon tumor incidence IAGP N RGD:5509061 20240111 MGI PMID:37459052 10166 Apc APC, WNT signaling pathway regulator gene MP:0012700 abnormal endocardial heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12645927 10166 Apc APC, WNT signaling pathway regulator gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20160714 MGI PMID:17418409 10166 Apc APC, WNT signaling pathway regulator gene MP:0013443 Harderian gland hyperplasia IAGP N RGD:5509061 20150205 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0013654 increased CD103-positive CD11b-low dendritic cell number IAGP N RGD:5509061 20160128 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0013751 increased cystadenoma incidence IAGP N RGD:5509061 20170615 MGI PMID:26411367 10166 Apc APC, WNT signaling pathway regulator gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:17332369 10166 Apc APC, WNT signaling pathway regulator gene MP:0014201 abnormal intestinal epithelium physiology IAGP N RGD:5509061 20220217 MGI PMID:34934045 10166 Apc APC, WNT signaling pathway regulator gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:20176656 10166 Apc APC, WNT signaling pathway regulator gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:23318432 10166 Apc APC, WNT signaling pathway regulator gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:29844172 10166 Apc APC, WNT signaling pathway regulator gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20240718 MGI PMID:35605119 10166 Apc APC, WNT signaling pathway regulator gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:12384562 10166 Apc APC, WNT signaling pathway regulator gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:16288217 10166 Apc APC, WNT signaling pathway regulator gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:17418409 10166 Apc APC, WNT signaling pathway regulator gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:26214133 10166 Apc APC, WNT signaling pathway regulator gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20240606 MGI PMID:31239271 10166 Apc APC, WNT signaling pathway regulator gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:19356224 10166 Apc APC, WNT signaling pathway regulator gene MP:0014353 abnormal gastrointestinal brush cell morphology IAGP N RGD:5509061 20240104 MGI PMID:26527802 10166 Apc APC, WNT signaling pathway regulator gene MP:0020324 jejunum polyps IAGP N RGD:5509061 20160714 MGI PMID:25578479 10166 Apc APC, WNT signaling pathway regulator gene MP:0020857 cornea epithelium hyperplasia IAGP N RGD:5509061 20181101 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0030053 increased forehead pigmentation IAGP N RGD:5509061 20170921 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:17002498 10166 Apc APC, WNT signaling pathway regulator gene MP:0031154 intestinal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:10783317 10166 Apc APC, WNT signaling pathway regulator gene MP:0031309 skin cyst IAGP N RGD:5509061 20211028 MGI PMID:10346819 10166 Apc APC, WNT signaling pathway regulator gene MP:0031309 skin cyst IAGP N RGD:5509061 20211028 MGI PMID:20176656 10167 Speg SPEG complex locus gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 10167 Speg SPEG complex locus gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0003057 abnormal epicardium morphology IAGP N RGD:5509061 20141003 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0004062 dilated heart right atrium IAGP N RGD:5509061 20141003 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0004063 dilated heart left atrium IAGP N RGD:5509061 20141003 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0031609 increased fetal cardiomyocyte size IAGP N RGD:5509061 20240509 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0031611 decreased fetal cardiomyocyte number IAGP N RGD:5509061 20240509 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0031614 fetal cardiomyocyte vacuoles IAGP N RGD:5509061 20240509 MGI PMID:19118250 10167 Speg SPEG complex locus gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:19118250 10170 Apeh acylpeptide hydrolase gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20190502 MGI 10170 Apeh acylpeptide hydrolase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 10170 Apeh acylpeptide hydrolase gene MP:0010052 increased grip strength IEA N RGD:5509061 20220519 MGI 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:9461064 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:19726636 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20693289 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20855613 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:23986861 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9461064 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9461064 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0001411 spinning IAGP N RGD:5509061 20141003 MGI PMID:9461064 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:9461064 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:9461064 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20140888 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9461064 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0002764 short tibia IEA N RGD:5509061 20221215 MGI 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:9461064 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9707424 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:19726636 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:9461064 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:9461064 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11050115 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20693289 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20855613 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20693289 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23986861 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9461064 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11050115 10172 Aplp2 amyloid beta precursor-like protein 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9707424 10173 Apoa1 apolipoprotein A-I gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10173 Apoa1 apolipoprotein A-I gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9186920 10173 Apoa1 apolipoprotein A-I gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12471038 10173 Apoa1 apolipoprotein A-I gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10173 Apoa1 apolipoprotein A-I gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:1496008 10173 Apoa1 apolipoprotein A-I gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9186920 10173 Apoa1 apolipoprotein A-I gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9743230 10173 Apoa1 apolipoprotein A-I gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9795222 10173 Apoa1 apolipoprotein A-I gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12937162 10173 Apoa1 apolipoprotein A-I gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:12471038 10173 Apoa1 apolipoprotein A-I gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12937162 10173 Apoa1 apolipoprotein A-I gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:12937162 10173 Apoa1 apolipoprotein A-I gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:12937162 10173 Apoa1 apolipoprotein A-I gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:12937162 10173 Apoa1 apolipoprotein A-I gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10173 Apoa1 apolipoprotein A-I gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9186920 10173 Apoa1 apolipoprotein A-I gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9743230 10173 Apoa1 apolipoprotein A-I gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9795222 10173 Apoa1 apolipoprotein A-I gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9743230 10173 Apoa1 apolipoprotein A-I gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20141003 MGI PMID:9684752 10173 Apoa1 apolipoprotein A-I gene MP:0003192 increased cholesterol efflux IAGP N RGD:5509061 20141003 MGI PMID:9743230 10173 Apoa1 apolipoprotein A-I gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20141003 MGI PMID:9186920 10173 Apoa1 apolipoprotein A-I gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20141003 MGI PMID:9743230 10173 Apoa1 apolipoprotein A-I gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:12937162 10173 Apoa1 apolipoprotein A-I gene MP:0003981 decreased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:9743230 10173 Apoa1 apolipoprotein A-I gene MP:0003981 decreased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:9795222 10173 Apoa1 apolipoprotein A-I gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10173 Apoa1 apolipoprotein A-I gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:16339487 10173 Apoa1 apolipoprotein A-I gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10173 Apoa1 apolipoprotein A-I gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9186920 10173 Apoa1 apolipoprotein A-I gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9743230 10173 Apoa1 apolipoprotein A-I gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9795222 10173 Apoa1 apolipoprotein A-I gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12471038 10173 Apoa1 apolipoprotein A-I gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10173 Apoa1 apolipoprotein A-I gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:1496008 10173 Apoa1 apolipoprotein A-I gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7751823 10173 Apoa1 apolipoprotein A-I gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9186920 10173 Apoa1 apolipoprotein A-I gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9743230 10173 Apoa1 apolipoprotein A-I gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9795222 10173 Apoa1 apolipoprotein A-I gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12471038 10173 Apoa1 apolipoprotein A-I gene MP:0008294 abnormal adrenal gland zona fasciculata morphology IAGP N RGD:5509061 20141003 MGI PMID:12937162 10173 Apoa1 apolipoprotein A-I gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10173 Apoa1 apolipoprotein A-I gene MP:0010072 increased pruritus IAGP N RGD:5509061 20141003 MGI PMID:12937162 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9598833 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16434491 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8692961 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9701246 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12235184 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8692961 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8824235 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9598833 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12816761 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20240523 MGI 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000692 small spleen IEA N RGD:5509061 20230119 MGI 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0001147 small testis IEA N RGD:5509061 20230119 MGI 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230119 MGI 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230119 MGI 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12235184 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9240444 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9598833 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9701246 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12235184 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20231207 MGI 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12816761 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8692961 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8626621 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:16434491 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9598833 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12235184 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9240444 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9598833 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9701246 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12235184 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9598833 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:9240444 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:16434491 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:9701246 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17155952 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0012223 increased circulating prothrombin level IAGP N RGD:5509061 20141003 MGI PMID:16434491 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0012326 increased circulating antithrombin level IAGP N RGD:5509061 20141003 MGI PMID:16434491 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0012355 decreased prothrombin time IAGP N RGD:5509061 20141003 MGI PMID:16434491 10174 Apobec1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 gene MP:0012358 decreased partial thromboplastin time IAGP N RGD:5509061 20201002 MGI PMID:16434491 10175 Apoc1 apolipoprotein C-I gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7848292 10175 Apoc1 apolipoprotein C-I gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:17053273 10175 Apoc1 apolipoprotein C-I gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:7848292 10175 Apoc1 apolipoprotein C-I gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17053273 10175 Apoc1 apolipoprotein C-I gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:17053273 10175 Apoc1 apolipoprotein C-I gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:17053273 10175 Apoc1 apolipoprotein C-I gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:17053273 10175 Apoc1 apolipoprotein C-I gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7581381 10175 Apoc1 apolipoprotein C-I gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7848292 10175 Apoc1 apolipoprotein C-I gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7581381 10175 Apoc1 apolipoprotein C-I gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17053273 10176 Apoc2 apolipoprotein C2 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20160505 MGI PMID:26574515 10176 Apoc2 apolipoprotein C2 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20160505 MGI PMID:26574515 10176 Apoc2 apolipoprotein C2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20160505 MGI PMID:26574515 10176 Apoc2 apolipoprotein C2 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20160505 MGI PMID:26574515 10176 Apoc2 apolipoprotein C2 gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20160505 MGI PMID:26574515 10176 Apoc2 apolipoprotein C2 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20160505 MGI PMID:26574515 10176 Apoc2 apolipoprotein C2 gene MP:0010329 abnormal lipoprotein level IAGP N RGD:5509061 20160505 MGI PMID:26574515 10179 Apoc3 apolipoprotein C-III gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15734841 10179 Apoc3 apolipoprotein C-III gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8089130 10179 Apoc3 apolipoprotein C-III gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8089130 10179 Apoc3 apolipoprotein C-III gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8089130 10179 Apoc3 apolipoprotein C-III gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15117734 10179 Apoc3 apolipoprotein C-III gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:15734841 10179 Apoc3 apolipoprotein C-III gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15734841 10179 Apoc3 apolipoprotein C-III gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:8089130 10179 Apoc3 apolipoprotein C-III gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:15734841 10179 Apoc3 apolipoprotein C-III gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8089130 10179 Apoc3 apolipoprotein C-III gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8089130 10179 Apoc3 apolipoprotein C-III gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15734841 10179 Apoc3 apolipoprotein C-III gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15734841 10179 Apoc3 apolipoprotein C-III gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15734841 10179 Apoc3 apolipoprotein C-III gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15734841 10179 Apoc3 apolipoprotein C-III gene MP:0008570 lipidosis IAGP N RGD:5509061 20141003 MGI PMID:15734841 10179 Apoc3 apolipoprotein C-III gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15734841 10179 Apoc3 apolipoprotein C-III gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:15734841 10180 Apod apolipoprotein D gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:24082102 10180 Apod apolipoprotein D gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18419796 10180 Apod apolipoprotein D gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:18419796 10180 Apod apolipoprotein D gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18419796 10180 Apod apolipoprotein D gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:18419796 10180 Apod apolipoprotein D gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:18419796 10180 Apod apolipoprotein D gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:24082102 10180 Apod apolipoprotein D gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18419796 10180 Apod apolipoprotein D gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:18419796 10180 Apod apolipoprotein D gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18419796 10180 Apod apolipoprotein D gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:24082102 10180 Apod apolipoprotein D gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18419796 10181 Aqp1 aquaporin 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210520 MGI 10181 Aqp1 aquaporin 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210128 MGI 10181 Aqp1 aquaporin 1 gene MP:0000226 abnormal mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:12133842 10181 Aqp1 aquaporin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9468475 10181 Aqp1 aquaporin 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15998844 10181 Aqp1 aquaporin 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20170105 MGI 10181 Aqp1 aquaporin 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 10181 Aqp1 aquaporin 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:9468475 10181 Aqp1 aquaporin 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 10181 Aqp1 aquaporin 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10613915 10181 Aqp1 aquaporin 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12133842 10181 Aqp1 aquaporin 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9468475 10181 Aqp1 aquaporin 1 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:15998844 10181 Aqp1 aquaporin 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:15998844 10181 Aqp1 aquaporin 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:10613915 10181 Aqp1 aquaporin 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11382807 10181 Aqp1 aquaporin 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:15998844 10181 Aqp1 aquaporin 1 gene MP:0002593 high mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12133842 10181 Aqp1 aquaporin 1 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12133842 10181 Aqp1 aquaporin 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20170105 MGI 10181 Aqp1 aquaporin 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:15647389 10181 Aqp1 aquaporin 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:15998844 10181 Aqp1 aquaporin 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:9468475 10181 Aqp1 aquaporin 1 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20230601 MGI 10181 Aqp1 aquaporin 1 gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:10613915 10181 Aqp1 aquaporin 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 10181 Aqp1 aquaporin 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:16582023 10181 Aqp1 aquaporin 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 10181 Aqp1 aquaporin 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:9468475 10181 Aqp1 aquaporin 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20170105 MGI 10181 Aqp1 aquaporin 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230601 MGI 10181 Aqp1 aquaporin 1 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 10181 Aqp1 aquaporin 1 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:9468475 10181 Aqp1 aquaporin 1 gene MP:0006423 dilated rete testis IAGP N RGD:5509061 20141003 MGI PMID:11698654 10181 Aqp1 aquaporin 1 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20190502 MGI 10181 Aqp1 aquaporin 1 gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:9468475 10181 Aqp1 aquaporin 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 10181 Aqp1 aquaporin 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 10181 Aqp1 aquaporin 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 10181 Aqp1 aquaporin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12133842 10181 Aqp1 aquaporin 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10400615 10181 Aqp1 aquaporin 1 gene MP:0011443 abnormal renal water transport IAGP N RGD:5509061 20141003 MGI PMID:15998844 10181 Aqp1 aquaporin 1 gene MP:0011443 abnormal renal water transport IAGP N RGD:5509061 20141003 MGI PMID:9468475 10182 Aqp2 aquaporin 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:3184310 10182 Aqp2 aquaporin 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:16121255 10182 Aqp2 aquaporin 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:16581908 10182 Aqp2 aquaporin 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:17229678 10182 Aqp2 aquaporin 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:3184310 10182 Aqp2 aquaporin 2 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:16434568 10182 Aqp2 aquaporin 2 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:16434568 10182 Aqp2 aquaporin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17229678 10182 Aqp2 aquaporin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:3184310 10182 Aqp2 aquaporin 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16968783 10182 Aqp2 aquaporin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:3184310 10182 Aqp2 aquaporin 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:3184310 10182 Aqp2 aquaporin 2 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:16121255 10182 Aqp2 aquaporin 2 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:17229678 10182 Aqp2 aquaporin 2 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:11035038 10182 Aqp2 aquaporin 2 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:17229678 10182 Aqp2 aquaporin 2 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:17229678 10182 Aqp2 aquaporin 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16581908 10182 Aqp2 aquaporin 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:11035038 10182 Aqp2 aquaporin 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:16121255 10182 Aqp2 aquaporin 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:16434568 10182 Aqp2 aquaporin 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:16581908 10182 Aqp2 aquaporin 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:16968783 10182 Aqp2 aquaporin 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:17229678 10182 Aqp2 aquaporin 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17229678 10182 Aqp2 aquaporin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:3184310 10182 Aqp2 aquaporin 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11035038 10182 Aqp2 aquaporin 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:3184310 10182 Aqp2 aquaporin 2 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:16121255 10182 Aqp2 aquaporin 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:17229678 10182 Aqp2 aquaporin 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:11035038 10182 Aqp2 aquaporin 2 gene MP:0002987 abnormal urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:16434568 10182 Aqp2 aquaporin 2 gene MP:0002987 abnormal urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:17229678 10182 Aqp2 aquaporin 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:11035038 10182 Aqp2 aquaporin 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:16121255 10182 Aqp2 aquaporin 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:16434568 10182 Aqp2 aquaporin 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:16581908 10182 Aqp2 aquaporin 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:16968783 10182 Aqp2 aquaporin 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:17229678 10182 Aqp2 aquaporin 2 gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:11035038 10182 Aqp2 aquaporin 2 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17229678 10182 Aqp2 aquaporin 2 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:17229678 10182 Aqp2 aquaporin 2 gene MP:0004192 abnormal kidney pyramid morphology IAGP N RGD:5509061 20141003 MGI PMID:3184310 10182 Aqp2 aquaporin 2 gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:11035038 10182 Aqp2 aquaporin 2 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:16434568 10182 Aqp2 aquaporin 2 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:17229678 10182 Aqp2 aquaporin 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:3184310 10182 Aqp2 aquaporin 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:11035038 10182 Aqp2 aquaporin 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17229678 10182 Aqp2 aquaporin 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:3184310 10182 Aqp2 aquaporin 2 gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:11035038 10182 Aqp2 aquaporin 2 gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16641094 10182 Aqp2 aquaporin 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11035038 10182 Aqp2 aquaporin 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16581908 10182 Aqp2 aquaporin 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16581908 10182 Aqp2 aquaporin 2 gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20141003 MGI PMID:11035038 10182 Aqp2 aquaporin 2 gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20141003 MGI PMID:16581908 10182 Aqp2 aquaporin 2 gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20141003 MGI PMID:17229678 10182 Aqp2 aquaporin 2 gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20141003 MGI PMID:3184310 10182 Aqp2 aquaporin 2 gene MP:0011305 dilated kidney calyx IAGP N RGD:5509061 20141003 MGI PMID:3184310 10182 Aqp2 aquaporin 2 gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20141003 MGI PMID:11035038 10182 Aqp2 aquaporin 2 gene MP:0011413 colorless urine IAGP N RGD:5509061 20141003 MGI PMID:3184310 10182 Aqp2 aquaporin 2 gene MP:0011422 kidney medulla atrophy IAGP N RGD:5509061 20141003 MGI PMID:11035038 10182 Aqp2 aquaporin 2 gene MP:0011422 kidney medulla atrophy IAGP N RGD:5509061 20141003 MGI PMID:16434568 10182 Aqp2 aquaporin 2 gene MP:0011422 kidney medulla atrophy IAGP N RGD:5509061 20141003 MGI PMID:3184310 10182 Aqp2 aquaporin 2 gene MP:0011492 ureterovesical junction obstruction IAGP N RGD:5509061 20141003 MGI PMID:3184310 10182 Aqp2 aquaporin 2 gene MP:0011844 kidney collecting duct atrophy IAGP N RGD:5509061 20141003 MGI PMID:16641094 10183 Aqp4 aquaporin 4 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220505 MGI PMID:18976758 10183 Aqp4 aquaporin 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10613915 10183 Aqp4 aquaporin 4 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:10737773 10183 Aqp4 aquaporin 4 gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:10655103 10183 Aqp4 aquaporin 4 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:16797122 10183 Aqp4 aquaporin 4 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220505 MGI PMID:18976758 10183 Aqp4 aquaporin 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220505 MGI PMID:18976758 10183 Aqp4 aquaporin 4 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11406631 10183 Aqp4 aquaporin 4 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:10613915 10183 Aqp4 aquaporin 4 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11382807 10183 Aqp4 aquaporin 4 gene MP:0002637 small uterus IAGP N RGD:5509061 20220505 MGI PMID:18976758 10183 Aqp4 aquaporin 4 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20220505 MGI PMID:18976758 10183 Aqp4 aquaporin 4 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:10737773 10183 Aqp4 aquaporin 4 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:9276712 10183 Aqp4 aquaporin 4 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:9486146 10183 Aqp4 aquaporin 4 gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:10613915 10183 Aqp4 aquaporin 4 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:16797122 10183 Aqp4 aquaporin 4 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19428702 10183 Aqp4 aquaporin 4 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20150205 MGI PMID:23428384 10183 Aqp4 aquaporin 4 gene MP:0004699 unilateral deafness IAGP N RGD:5509061 20141003 MGI PMID:12359252 10183 Aqp4 aquaporin 4 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220505 MGI PMID:18976758 10183 Aqp4 aquaporin 4 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20220505 MGI PMID:18976758 10183 Aqp4 aquaporin 4 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:23277579 10183 Aqp4 aquaporin 4 gene MP:0005167 abnormal blood-brain barrier function IAGP N RGD:5509061 20141003 MGI PMID:21990350 10183 Aqp4 aquaporin 4 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11818406 10183 Aqp4 aquaporin 4 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15557457 10183 Aqp4 aquaporin 4 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:10655103 10183 Aqp4 aquaporin 4 gene MP:0006190 retina ischemia IAGP N RGD:5509061 20141003 MGI PMID:15557457 10183 Aqp4 aquaporin 4 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:11406631 10183 Aqp4 aquaporin 4 gene MP:0008258 thin endometrium IAGP N RGD:5509061 20220505 MGI PMID:18976758 10183 Aqp4 aquaporin 4 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16797122 10183 Aqp4 aquaporin 4 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21187412 10183 Aqp4 aquaporin 4 gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20220505 MGI PMID:18976758 10183 Aqp4 aquaporin 4 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:16797122 10183 Aqp4 aquaporin 4 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10655103 10183 Aqp4 aquaporin 4 gene MP:0010750 increased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23277579 10183 Aqp4 aquaporin 4 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220505 MGI PMID:18976758 10183 Aqp4 aquaporin 4 gene MP:0011443 abnormal renal water transport IAGP N RGD:5509061 20141003 MGI PMID:9486146 10183 Aqp4 aquaporin 4 gene MP:0011854 cerebral edema IAGP N RGD:5509061 20141003 MGI PMID:23277579 10183 Aqp4 aquaporin 4 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:11406631 10183 Aqp4 aquaporin 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11406631 10183 Aqp4 aquaporin 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12359252 10183 Aqp4 aquaporin 4 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:18976758 10184 Aqp5 aquaporin 5 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:10400615 10184 Aqp5 aquaporin 5 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:11290736 10184 Aqp5 aquaporin 5 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:15647389 10184 Aqp5 aquaporin 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11290736 10184 Aqp5 aquaporin 5 gene MP:0001337 dry eyes IAGP N RGD:5509061 20220721 MGI PMID:33013441 10184 Aqp5 aquaporin 5 gene MP:0001346 abnormal lacrimal gland morphology IAGP N RGD:5509061 20220721 MGI PMID:33013441 10184 Aqp5 aquaporin 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10400615 10184 Aqp5 aquaporin 5 gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:11290736 10184 Aqp5 aquaporin 5 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:11707570 10184 Aqp5 aquaporin 5 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11382807 10184 Aqp5 aquaporin 5 gene MP:0005310 abnormal salivary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:10400615 10184 Aqp5 aquaporin 5 gene MP:0005310 abnormal salivary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:11290736 10184 Aqp5 aquaporin 5 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20220721 MGI PMID:33013441 10184 Aqp5 aquaporin 5 gene MP:0010896 decreased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:11707570 10184 Aqp5 aquaporin 5 gene MP:0010935 increased airway resistance IAGP N RGD:5509061 20141003 MGI PMID:11707570 10184 Aqp5 aquaporin 5 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10400615 10184 Aqp5 aquaporin 5 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11290736 10184 Aqp5 aquaporin 5 gene MP:0012124 increased bronchoconstrictive response IAGP N RGD:5509061 20141003 MGI PMID:11707570 10184 Aqp5 aquaporin 5 gene MP:0014525 impaired pulmonary alveolar fluid clearance IAGP N RGD:5509061 20240912 MGI PMID:27064541 10184 Aqp5 aquaporin 5 gene MP:0020220 decreased tear production IAGP N RGD:5509061 20220721 MGI PMID:33013441 10187 Ar androgen receptor gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22415878 10187 Ar androgen receptor gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12943692 10187 Ar androgen receptor gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:9647203 10187 Ar androgen receptor gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:9647203 10187 Ar androgen receptor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15961403 10187 Ar androgen receptor gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20150618 MGI PMID:2055107 10187 Ar androgen receptor gene MP:0000440 domed cranium IAGP N RGD:5509061 20150618 MGI PMID:2055107 10187 Ar androgen receptor gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0000562 polydactyly IAGP N RGD:5509061 20150618 MGI PMID:2055107 10187 Ar androgen receptor gene MP:0000564 syndactyly IAGP N RGD:5509061 20150618 MGI PMID:2055107 10187 Ar androgen receptor gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:14676301 10187 Ar androgen receptor gene MP:0000661 small prostate gland ventral lobe IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:14676301 10187 Ar androgen receptor gene MP:0000664 small prostate gland anterior lobe IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:14676301 10187 Ar androgen receptor gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0000914 exencephaly IAGP N RGD:5509061 20150618 MGI PMID:2055107 10187 Ar androgen receptor gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10319319 10187 Ar androgen receptor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:5452809 10187 Ar androgen receptor gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:5452809 10187 Ar androgen receptor gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10319319 10187 Ar androgen receptor gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:5452809 10187 Ar androgen receptor gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:7954809 10187 Ar androgen receptor gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:11090455 10187 Ar androgen receptor gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:14701682 10187 Ar androgen receptor gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:16400023 10187 Ar androgen receptor gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:19574395 10187 Ar androgen receptor gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:21084446 10187 Ar androgen receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:14701682 10187 Ar androgen receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15107499 10187 Ar androgen receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17142319 10187 Ar androgen receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23759306 10187 Ar androgen receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:5452809 10187 Ar androgen receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:7967466 10187 Ar androgen receptor gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:21084446 10187 Ar androgen receptor gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:18401008 10187 Ar androgen receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:17142319 10187 Ar androgen receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:17360365 10187 Ar androgen receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:19574395 10187 Ar androgen receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:21383160 10187 Ar androgen receptor gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:17142319 10187 Ar androgen receptor gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:21084446 10187 Ar androgen receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12943692 10187 Ar androgen receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15107499 10187 Ar androgen receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17142319 10187 Ar androgen receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19574395 10187 Ar androgen receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:7954809 10187 Ar androgen receptor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11090455 10187 Ar androgen receptor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15107499 10187 Ar androgen receptor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16400023 10187 Ar androgen receptor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19574395 10187 Ar androgen receptor gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17652515 10187 Ar androgen receptor gene MP:0001159 absent prostate gland IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0001159 absent prostate gland IAGP N RGD:5509061 20141003 MGI PMID:12943692 10187 Ar androgen receptor gene MP:0001159 absent prostate gland IAGP N RGD:5509061 20141003 MGI PMID:15107499 10187 Ar androgen receptor gene MP:0001159 absent prostate gland IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0001159 absent prostate gland IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0001163 abnormal prostate gland anterior lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17652515 10187 Ar androgen receptor gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:12943692 10187 Ar androgen receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16601069 10187 Ar androgen receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:7967466 10187 Ar androgen receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12943692 10187 Ar androgen receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20150618 MGI PMID:2055107 10187 Ar androgen receptor gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:14676301 10187 Ar androgen receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22415878 10187 Ar androgen receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:22415878 10187 Ar androgen receptor gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12943692 10187 Ar androgen receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:14701682 10187 Ar androgen receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15107499 10187 Ar androgen receptor gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:14701682 10187 Ar androgen receptor gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:15107499 10187 Ar androgen receptor gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:15919750 10187 Ar androgen receptor gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:16400023 10187 Ar androgen receptor gene MP:0001875 testis inflammation IAGP N RGD:5509061 20141003 MGI PMID:21084446 10187 Ar androgen receptor gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:14676301 10187 Ar androgen receptor gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:12943692 10187 Ar androgen receptor gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:21383160 10187 Ar androgen receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:16400023 10187 Ar androgen receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17360365 10187 Ar androgen receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15107499 10187 Ar androgen receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17142319 10187 Ar androgen receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19574395 10187 Ar androgen receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21084446 10187 Ar androgen receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:7967466 10187 Ar androgen receptor gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:5452809 10187 Ar androgen receptor gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:17142319 10187 Ar androgen receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17360365 10187 Ar androgen receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:12943692 10187 Ar androgen receptor gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:14701682 10187 Ar androgen receptor gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:18401008 10187 Ar androgen receptor gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:23759306 10187 Ar androgen receptor gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:5452809 10187 Ar androgen receptor gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:7954809 10187 Ar androgen receptor gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:7967466 10187 Ar androgen receptor gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:17406000 10187 Ar androgen receptor gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16601069 10187 Ar androgen receptor gene MP:0002059 abnormal seminal vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20150618 MGI PMID:2055107 10187 Ar androgen receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22415878 10187 Ar androgen receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21383160 10187 Ar androgen receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15294140 10187 Ar androgen receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17360365 10187 Ar androgen receptor gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:15961403 10187 Ar androgen receptor gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:17360365 10187 Ar androgen receptor gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:10319319 10187 Ar androgen receptor gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:5452809 10187 Ar androgen receptor gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:7954809 10187 Ar androgen receptor gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:7967466 10187 Ar androgen receptor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:14701682 10187 Ar androgen receptor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15107499 10187 Ar androgen receptor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17142319 10187 Ar androgen receptor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18401008 10187 Ar androgen receptor gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:12943692 10187 Ar androgen receptor gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:14701682 10187 Ar androgen receptor gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:17142319 10187 Ar androgen receptor gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:18401008 10187 Ar androgen receptor gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:5452809 10187 Ar androgen receptor gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:7954809 10187 Ar androgen receptor gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:5452809 10187 Ar androgen receptor gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:21084446 10187 Ar androgen receptor gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:21084446 10187 Ar androgen receptor gene MP:0002661 abnormal corpus epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0002669 abnormal scrotum morphology IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0002670 absent scrotum IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0002673 abnormal sperm number IAGP N RGD:5509061 20141003 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:14701682 10187 Ar androgen receptor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16400023 10187 Ar androgen receptor gene MP:0002774 small prostate gland IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0002774 small prostate gland IAGP N RGD:5509061 20141003 MGI PMID:21383160 10187 Ar androgen receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:15107499 10187 Ar androgen receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17142319 10187 Ar androgen receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:14701682 10187 Ar androgen receptor gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:21383160 10187 Ar androgen receptor gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16400023 10187 Ar androgen receptor gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17142319 10187 Ar androgen receptor gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15919750 10187 Ar androgen receptor gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19574395 10187 Ar androgen receptor gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:10319319 10187 Ar androgen receptor gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:14701682 10187 Ar androgen receptor gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:5452809 10187 Ar androgen receptor gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:7954809 10187 Ar androgen receptor gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20150618 MGI PMID:2055107 10187 Ar androgen receptor gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:16400023 10187 Ar androgen receptor gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:15961403 10187 Ar androgen receptor gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0003124 hypospadia IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:16400023 10187 Ar androgen receptor gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:21084446 10187 Ar androgen receptor gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:17406000 10187 Ar androgen receptor gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:21383160 10187 Ar androgen receptor gene MP:0003534 blind vagina IAGP N RGD:5509061 20141003 MGI PMID:12943692 10187 Ar androgen receptor gene MP:0003550 short perineum IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0003553 abnormal foreskin morphology IAGP N RGD:5509061 20141003 MGI PMID:19282366 10187 Ar androgen receptor gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:10319319 10187 Ar androgen receptor gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:12943692 10187 Ar androgen receptor gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:5452809 10187 Ar androgen receptor gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:7954809 10187 Ar androgen receptor gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:21383160 10187 Ar androgen receptor gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:12943692 10187 Ar androgen receptor gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:15107499 10187 Ar androgen receptor gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:15919750 10187 Ar androgen receptor gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:21084446 10187 Ar androgen receptor gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21383160 10187 Ar androgen receptor gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15961403 10187 Ar androgen receptor gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20141003 MGI PMID:19282366 10187 Ar androgen receptor gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17406000 10187 Ar androgen receptor gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:15961403 10187 Ar androgen receptor gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:10319319 10187 Ar androgen receptor gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:12943692 10187 Ar androgen receptor gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:15107499 10187 Ar androgen receptor gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:5452809 10187 Ar androgen receptor gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:7954809 10187 Ar androgen receptor gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18401008 10187 Ar androgen receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:14701682 10187 Ar androgen receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15107499 10187 Ar androgen receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15919750 10187 Ar androgen receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16400023 10187 Ar androgen receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17360365 10187 Ar androgen receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19574395 10187 Ar androgen receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:14676301 10187 Ar androgen receptor gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:15107499 10187 Ar androgen receptor gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:14676301 10187 Ar androgen receptor gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:14701682 10187 Ar androgen receptor gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:17360365 10187 Ar androgen receptor gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:17360365 10187 Ar androgen receptor gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21084446 10187 Ar androgen receptor gene MP:0004934 epididymis epithelium degeneration IAGP N RGD:5509061 20141003 MGI PMID:21084446 10187 Ar androgen receptor gene MP:0004961 increased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:21383160 10187 Ar androgen receptor gene MP:0004962 decreased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0004962 decreased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:21383160 10187 Ar androgen receptor gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0005117 increased circulating pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:14701682 10187 Ar androgen receptor gene MP:0005149 abnormal gubernaculum morphology IAGP N RGD:5509061 20141003 MGI PMID:10319319 10187 Ar androgen receptor gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:14701682 10187 Ar androgen receptor gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:15107499 10187 Ar androgen receptor gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:17142319 10187 Ar androgen receptor gene MP:0005187 abnormal penis morphology IAGP N RGD:5509061 20141003 MGI PMID:12943692 10187 Ar androgen receptor gene MP:0005188 small penis IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20141003 MGI PMID:5452809 10187 Ar androgen receptor gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20141003 MGI PMID:17360365 10187 Ar androgen receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22415878 10187 Ar androgen receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22415878 10187 Ar androgen receptor gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22415878 10187 Ar androgen receptor gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:16601069 10187 Ar androgen receptor gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:15919750 10187 Ar androgen receptor gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15961403 10187 Ar androgen receptor gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18401008 10187 Ar androgen receptor gene MP:0006308 enlarged seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:18401008 10187 Ar androgen receptor gene MP:0006369 supernumerary incisors IAGP N RGD:5509061 20150618 MGI PMID:2055107 10187 Ar androgen receptor gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17142319 10187 Ar androgen receptor gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0006420 abnormal peritubular myoid cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9647203 10187 Ar androgen receptor gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9647203 10187 Ar androgen receptor gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:14701682 10187 Ar androgen receptor gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:15107499 10187 Ar androgen receptor gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:16326839 10187 Ar androgen receptor gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17142319 10187 Ar androgen receptor gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18401008 10187 Ar androgen receptor gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:5452809 10187 Ar androgen receptor gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0009066 decreased oviduct weight IAGP N RGD:5509061 20141003 MGI PMID:14676301 10187 Ar androgen receptor gene MP:0009073 absent Wolffian ducts IAGP N RGD:5509061 20141003 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0009198 abnormal male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:21084446 10187 Ar androgen receptor gene MP:0009199 abnormal external male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0009199 abnormal external male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:19282366 10187 Ar androgen receptor gene MP:0009204 absent external male genitalia IAGP N RGD:5509061 20141003 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21620777 10187 Ar androgen receptor gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22415878 10187 Ar androgen receptor gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22415878 10187 Ar androgen receptor gene MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22415878 10187 Ar androgen receptor gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0009659 striated fur IAGP N RGD:5509061 20150618 MGI PMID:2055107 10187 Ar androgen receptor gene MP:0010031 abnormal cranium size IAGP N RGD:5509061 20150618 MGI PMID:2055107 10187 Ar androgen receptor gene MP:0010045 increased omental fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22415878 10187 Ar androgen receptor gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20240627 MGI PMID:33870126 10187 Ar androgen receptor gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:22415878 10187 Ar androgen receptor gene MP:0010231 transverse fur striping IAGP N RGD:5509061 20150618 MGI PMID:2055107 10187 Ar androgen receptor gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:21383160 10187 Ar androgen receptor gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16601069 10187 Ar androgen receptor gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21383160 10187 Ar androgen receptor gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20150618 MGI PMID:2055107 10187 Ar androgen receptor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20150618 MGI PMID:2055107 10187 Ar androgen receptor gene MP:0011532 decreased urine major urinary protein level IAGP N RGD:5509061 20141003 MGI PMID:16400023 10187 Ar androgen receptor gene MP:0011533 increased urine major urinary protein level IAGP N RGD:5509061 20141003 MGI PMID:16981011 10187 Ar androgen receptor gene MP:0013288 premature acrosome reaction IAGP N RGD:5509061 20191226 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0013598 Leydig cell hypertrophy IAGP N RGD:5509061 20150319 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0013598 Leydig cell hypertrophy IAGP N RGD:5509061 20150319 MGI PMID:19574395 10187 Ar androgen receptor gene MP:0013598 Leydig cell hypertrophy IAGP N RGD:5509061 20150319 MGI PMID:5452809 10187 Ar androgen receptor gene MP:0013600 testis degeneration IAGP N RGD:5509061 20150312 MGI PMID:12943692 10187 Ar androgen receptor gene MP:0013604 abnormal adult Leydig cell differentiation IAGP N RGD:5509061 20150319 MGI PMID:11090455 10187 Ar androgen receptor gene MP:0013899 abnormal seminal vesicle epithelium morphology IAGP N RGD:5509061 20150924 MGI PMID:17317769 10187 Ar androgen receptor gene MP:0013899 abnormal seminal vesicle epithelium morphology IAGP N RGD:5509061 20150924 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0013904 abnormal seminal vesicle muscle layer morphology IAGP N RGD:5509061 20150924 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:14745012 10187 Ar androgen receptor gene MP:0014441 decreased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0014491 abnormal mammary gland sensory innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:23224557 10187 Ar androgen receptor gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:12370412 10187 Ar androgen receptor gene MP:0020355 abnormal Sertoli cell barrier morphology IAGP N RGD:5509061 20160915 MGI PMID:24825397 10187 Ar androgen receptor gene MP:0020356 abnormal Sertoli cell barrier function IAGP N RGD:5509061 20160915 MGI PMID:24825397 10187 Ar androgen receptor gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20161013 MGI PMID:16400023 10187 Ar androgen receptor gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:15961403 10187 Ar androgen receptor gene MP:0031287 bilateral cryptorchism IAGP N RGD:5509061 20211014 MGI PMID:10319319 10187 Ar androgen receptor gene MP:0031357 enlarged prostate gland ventral lobe IAGP N RGD:5509061 20220303 MGI PMID:17652515 10187 Ar androgen receptor gene MP:0031359 decreased prostate gland anterior lobe weight IAGP N RGD:5509061 20220303 MGI PMID:17360365 10187 Ar androgen receptor gene MP:0031362 decreased prostate gland ventral lobe weight IAGP N RGD:5509061 20220303 MGI PMID:17360365 10187 Ar androgen receptor gene MP:0031364 increased prostate gland ventral lobe weight IAGP N RGD:5509061 20220303 MGI PMID:21383160 10187 Ar androgen receptor gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:15919793 10187 Ar androgen receptor gene MP:0031435 abnormal copulatory plug biosynthesis IAGP N RGD:5509061 20220922 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0031436 decreased copulatory plug deposition IAGP N RGD:5509061 20220922 MGI PMID:18356274 10187 Ar androgen receptor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15961403 10188 Araf Araf proto-oncogene, serine/threonine kinase gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:8805280 10188 Araf Araf proto-oncogene, serine/threonine kinase gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:8805280 10188 Araf Araf proto-oncogene, serine/threonine kinase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:8805280 10188 Araf Araf proto-oncogene, serine/threonine kinase gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:8805280 10188 Araf Araf proto-oncogene, serine/threonine kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8805280 10188 Araf Araf proto-oncogene, serine/threonine kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8805280 10188 Araf Araf proto-oncogene, serine/threonine kinase gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:8805280 10188 Araf Araf proto-oncogene, serine/threonine kinase gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:8805280 10188 Araf Araf proto-oncogene, serine/threonine kinase gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:8805280 10188 Araf Araf proto-oncogene, serine/threonine kinase gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:8805280 10188 Araf Araf proto-oncogene, serine/threonine kinase gene MP:0001527 athetotic walking movements IAGP N RGD:5509061 20141003 MGI PMID:8805280 10188 Araf Araf proto-oncogene, serine/threonine kinase gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8805280 10188 Araf Araf proto-oncogene, serine/threonine kinase gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:8805280 10188 Araf Araf proto-oncogene, serine/threonine kinase gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:8805280 10188 Araf Araf proto-oncogene, serine/threonine kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8805280 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:21419768 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:9121557 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:9398442 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9398442 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11892012 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:14597763 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:14597763 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:14530333 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:14597763 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10521392 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9121557 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:9398442 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:11124810 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:9121557 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:9121557 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:9121557 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:14530333 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:11892012 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14764592 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11892012 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9398442 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11043581 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9398442 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20220519 MGI 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15798202 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:14597763 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:21419768 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21419768 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:9398442 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:11124810 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9121557 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9398442 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0004004 patent ductus venosus IAGP N RGD:5509061 20141003 MGI PMID:15545609 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:21419768 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9398442 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11124810 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0004560 abnormal chorionic plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11124810 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11124810 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11124810 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:14597763 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:11892012 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11043581 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:14530333 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:14764592 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14597763 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0009605 decreased keratohyalin granule number IAGP N RGD:5509061 20141003 MGI PMID:14597763 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14530333 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14597763 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9121557 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9398442 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14764592 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11381139 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:11892012 10189 Arnt aryl hydrocarbon receptor nuclear translocator gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:9398442 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:11381139 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0001257 increased body length IAGP N RGD:5509061 20190124 MGI PMID:30563851 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20190124 MGI PMID:30563851 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0001264 increased body size IAGP N RGD:5509061 20190124 MGI PMID:30563851 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0001433 polyphagia IAGP N RGD:5509061 20190124 MGI PMID:30563851 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0001746 abnormal pituitary secretion IAGP N RGD:5509061 20141003 MGI PMID:11318878 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20190124 MGI PMID:30563851 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20190124 MGI PMID:30563851 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20190124 MGI PMID:30563851 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0003965 abnormal pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:11318878 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0004164 abnormal neurohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:11318878 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20190124 MGI PMID:30563851 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11381139 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:11318878 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0008845 abnormal paraventricular hypothalamic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11318878 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0008846 abnormal supraoptic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11318878 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20190124 MGI PMID:30563851 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11318878 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11381139 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11381139 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11381139 10190 Arnt2 aryl hydrocarbon receptor nuclear translocator 2 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20190124 MGI PMID:30563851 10191 Arrb1 arrestin, beta 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 10191 Arrb1 arrestin, beta 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:9400383 10191 Arrb1 arrestin, beta 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0002274 abnormal type I pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:9400383 10191 Arrb1 arrestin, beta 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 10191 Arrb1 arrestin, beta 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20160421 MGI 10191 Arrb1 arrestin, beta 1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 10191 Arrb1 arrestin, beta 1 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 10191 Arrb1 arrestin, beta 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0011148 decreased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:20060823 10191 Arrb1 arrestin, beta 1 gene MP:0031635 increased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:9400383 10192 Arrb2 arrestin, beta 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20220519 MGI 10192 Arrb2 arrestin, beta 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160421 MGI 10192 Arrb2 arrestin, beta 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210520 MGI 10192 Arrb2 arrestin, beta 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10617462 10192 Arrb2 arrestin, beta 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:10617462 10192 Arrb2 arrestin, beta 2 gene MP:0002274 abnormal type I pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 10192 Arrb2 arrestin, beta 2 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:12032308 10192 Arrb2 arrestin, beta 2 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:16378096 10192 Arrb2 arrestin, beta 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 10192 Arrb2 arrestin, beta 2 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0008552 abnormal circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16378096 10192 Arrb2 arrestin, beta 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16378096 10192 Arrb2 arrestin, beta 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:16378096 10192 Arrb2 arrestin, beta 2 gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:16378096 10192 Arrb2 arrestin, beta 2 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:16378096 10192 Arrb2 arrestin, beta 2 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16378096 10192 Arrb2 arrestin, beta 2 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 10192 Arrb2 arrestin, beta 2 gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:20060823 10192 Arrb2 arrestin, beta 2 gene MP:0011148 decreased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:20060823 10193 Arsb arylsulfatase B gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20111116 MGI 10193 Arsb arylsulfatase B gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:12904606 10193 Arsb arylsulfatase B gene MP:0000346 broad head IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12904606 10193 Arsb arylsulfatase B gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0000441 increased cranium width IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0000588 thick tail IEA N RGD:5509061 20111116 MGI 10193 Arsb arylsulfatase B gene MP:0000958 peripheral nervous system degeneration IEA N RGD:5509061 20111116 MGI 10193 Arsb arylsulfatase B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 10193 Arsb arylsulfatase B gene MP:0001300 ocular hypertelorism IEA N RGD:5509061 20111116 MGI 10193 Arsb arylsulfatase B gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:12904606 10193 Arsb arylsulfatase B gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 10193 Arsb arylsulfatase B gene MP:0001921 reduced fertility IEA N RGD:5509061 20111116 MGI 10193 Arsb arylsulfatase B gene MP:0001935 decreased litter size IEA N RGD:5509061 20111116 MGI 10193 Arsb arylsulfatase B gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20111116 MGI 10193 Arsb arylsulfatase B gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 10193 Arsb arylsulfatase B gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12904606 10193 Arsb arylsulfatase B gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 10193 Arsb arylsulfatase B gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0003172 abnormal lysosome physiology IEA N RGD:5509061 20111116 MGI 10193 Arsb arylsulfatase B gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:12904606 10193 Arsb arylsulfatase B gene MP:0003958 heart valve hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12904606 10193 Arsb arylsulfatase B gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12904606 10193 Arsb arylsulfatase B gene MP:0005459 decreased percent body fat/body weight IEA N RGD:5509061 20111116 MGI 10193 Arsb arylsulfatase B gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12904606 10193 Arsb arylsulfatase B gene MP:0006045 mitral valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:12904606 10193 Arsb arylsulfatase B gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0009415 skeletal muscle degeneration IEA N RGD:5509061 20111116 MGI 10193 Arsb arylsulfatase B gene MP:0010620 thick mitral valve IAGP N RGD:5509061 20231221 MGI PMID:12904606 10193 Arsb arylsulfatase B gene MP:0011473 increased urine glycosaminoglycan level IAGP N RGD:5509061 20141003 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20141003 MGI 10193 Arsb arylsulfatase B gene MP:0020242 increased autopod size IAGP N RGD:5509061 20230824 MGI PMID:8710849 10193 Arsb arylsulfatase B gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:12904606 10193 Arsb arylsulfatase B gene MP:0020859 disorganized cornea epithelium IAGP N RGD:5509061 20181101 MGI PMID:12904606 10193 Arsb arylsulfatase B gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:12904606 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:8090202 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19684026 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:7773285 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:8090202 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:7773285 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:18039841 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7773285 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:19269367 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19269367 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:8090202 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7773285 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7773285 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8090202 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0012100 absent spongiotrophoblast IAGP N RGD:5509061 20141003 MGI PMID:7773285 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0012100 absent spongiotrophoblast IAGP N RGD:5509061 20141003 MGI PMID:8090202 10194 Ascl2 achaete-scute family bHLH transcription factor 2 gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20191219 MGI PMID:10495277 10197 Asgr1 asialoglycoprotein receptor 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:11278827 10197 Asgr1 asialoglycoprotein receptor 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18488037 10197 Asgr1 asialoglycoprotein receptor 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:22527485 10197 Asgr1 asialoglycoprotein receptor 1 gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:18488037 10197 Asgr1 asialoglycoprotein receptor 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18488037 10198 Atf3 activating transcription factor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23921126 10198 Atf3 activating transcription factor 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 10198 Atf3 activating transcription factor 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 10198 Atf3 activating transcription factor 3 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18794337 10198 Atf3 activating transcription factor 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23921126 10198 Atf3 activating transcription factor 3 gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:15199129 10198 Atf3 activating transcription factor 3 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:18794337 10198 Atf3 activating transcription factor 3 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:18794337 10198 Atf3 activating transcription factor 3 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:18794337 10198 Atf3 activating transcription factor 3 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:18794337 10198 Atf3 activating transcription factor 3 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:18794337 10198 Atf3 activating transcription factor 3 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20160714 MGI PMID:23462798 10198 Atf3 activating transcription factor 3 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20160714 MGI PMID:23462798 10199 Atm ataxia telangiectasia mutated gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20150806 MGI PMID:25683718 10199 Atm ataxia telangiectasia mutated gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20180125 MGI PMID:26310626 10199 Atm ataxia telangiectasia mutated gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:8917548 10199 Atm ataxia telangiectasia mutated gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8917548 10199 Atm ataxia telangiectasia mutated gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20211021 MGI PMID:31285322 10199 Atm ataxia telangiectasia mutated gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9356511 10199 Atm ataxia telangiectasia mutated gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10449794 10199 Atm ataxia telangiectasia mutated gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14673010 10199 Atm ataxia telangiectasia mutated gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:9356511 10199 Atm ataxia telangiectasia mutated gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:8917548 10199 Atm ataxia telangiectasia mutated gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:8917548 10199 Atm ataxia telangiectasia mutated gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15122331 10199 Atm ataxia telangiectasia mutated gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17967868 10199 Atm ataxia telangiectasia mutated gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24709420 10199 Atm ataxia telangiectasia mutated gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8917548 10199 Atm ataxia telangiectasia mutated gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11040211 10199 Atm ataxia telangiectasia mutated gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8917548 10199 Atm ataxia telangiectasia mutated gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19171781 10199 Atm ataxia telangiectasia mutated gene MP:0001393 ataxia IAGP N RGD:5509061 20180125 MGI PMID:26310626 10199 Atm ataxia telangiectasia mutated gene MP:0001393 ataxia IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001405 impaired coordination IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0001406 abnormal gait IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0001523 impaired righting response IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16357220 10199 Atm ataxia telangiectasia mutated gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:15122331 10199 Atm ataxia telangiectasia mutated gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20170413 MGI PMID:27798842 10199 Atm ataxia telangiectasia mutated gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0001798 impaired macrophage phagocytosis IEA N RGD:5509061 20190418 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0001830 decreased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20161013 MGI PMID:26290337 10199 Atm ataxia telangiectasia mutated gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:9582124 10199 Atm ataxia telangiectasia mutated gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8917548 10199 Atm ataxia telangiectasia mutated gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:8843193 10199 Atm ataxia telangiectasia mutated gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24709420 10199 Atm ataxia telangiectasia mutated gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12195425 10199 Atm ataxia telangiectasia mutated gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17158963 10199 Atm ataxia telangiectasia mutated gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15122331 10199 Atm ataxia telangiectasia mutated gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16357220 10199 Atm ataxia telangiectasia mutated gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24709420 10199 Atm ataxia telangiectasia mutated gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20180125 MGI PMID:26310626 10199 Atm ataxia telangiectasia mutated gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20211021 MGI PMID:31285322 10199 Atm ataxia telangiectasia mutated gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:12195425 10199 Atm ataxia telangiectasia mutated gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12195425 10199 Atm ataxia telangiectasia mutated gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19171781 10199 Atm ataxia telangiectasia mutated gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15122331 10199 Atm ataxia telangiectasia mutated gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16357220 10199 Atm ataxia telangiectasia mutated gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17158963 10199 Atm ataxia telangiectasia mutated gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17967868 10199 Atm ataxia telangiectasia mutated gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24709420 10199 Atm ataxia telangiectasia mutated gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0002083 premature death IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8917548 10199 Atm ataxia telangiectasia mutated gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:24709420 10199 Atm ataxia telangiectasia mutated gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20150212 MGI PMID:24532689 10199 Atm ataxia telangiectasia mutated gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20826531 10199 Atm ataxia telangiectasia mutated gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0002494 increased IgM level IEA N RGD:5509061 20181011 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0002619 abnormal lymphocyte morphology IEA N RGD:5509061 20190418 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20150806 MGI PMID:25683718 10199 Atm ataxia telangiectasia mutated gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22266795 10199 Atm ataxia telangiectasia mutated gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11040211 10199 Atm ataxia telangiectasia mutated gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11040211 10199 Atm ataxia telangiectasia mutated gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16777961 10199 Atm ataxia telangiectasia mutated gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:12192050 10199 Atm ataxia telangiectasia mutated gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:20194434 10199 Atm ataxia telangiectasia mutated gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:9356511 10199 Atm ataxia telangiectasia mutated gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24709420 10199 Atm ataxia telangiectasia mutated gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:22266795 10199 Atm ataxia telangiectasia mutated gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:10449794 10199 Atm ataxia telangiectasia mutated gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9356511 10199 Atm ataxia telangiectasia mutated gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:21368836 10199 Atm ataxia telangiectasia mutated gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16357220 10199 Atm ataxia telangiectasia mutated gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20826531 10199 Atm ataxia telangiectasia mutated gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:16357220 10199 Atm ataxia telangiectasia mutated gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:8917548 10199 Atm ataxia telangiectasia mutated gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:18599436 10199 Atm ataxia telangiectasia mutated gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:19450527 10199 Atm ataxia telangiectasia mutated gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:10677503 10199 Atm ataxia telangiectasia mutated gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:12192050 10199 Atm ataxia telangiectasia mutated gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:16357220 10199 Atm ataxia telangiectasia mutated gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:8843193 10199 Atm ataxia telangiectasia mutated gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9356511 10199 Atm ataxia telangiectasia mutated gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20161013 MGI PMID:26290337 10199 Atm ataxia telangiectasia mutated gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17429352 10199 Atm ataxia telangiectasia mutated gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:19171781 10199 Atm ataxia telangiectasia mutated gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:22266795 10199 Atm ataxia telangiectasia mutated gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:9582124 10199 Atm ataxia telangiectasia mutated gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:19450527 10199 Atm ataxia telangiectasia mutated gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22869596 10199 Atm ataxia telangiectasia mutated gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20170413 MGI PMID:27798842 10199 Atm ataxia telangiectasia mutated gene MP:0004849 abnormal testis size IAGP N RGD:5509061 20150212 MGI PMID:24532689 10199 Atm ataxia telangiectasia mutated gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20190418 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0005014 increased B cell number IAGP N RGD:5509061 20180125 MGI PMID:26310626 10199 Atm ataxia telangiectasia mutated gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170413 MGI PMID:27798842 10199 Atm ataxia telangiectasia mutated gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20211021 MGI PMID:31285322 10199 Atm ataxia telangiectasia mutated gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20170413 MGI PMID:27798842 10199 Atm ataxia telangiectasia mutated gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20180125 MGI PMID:26310626 10199 Atm ataxia telangiectasia mutated gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20211021 MGI PMID:31285322 10199 Atm ataxia telangiectasia mutated gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:10639172 10199 Atm ataxia telangiectasia mutated gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8917548 10199 Atm ataxia telangiectasia mutated gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20180125 MGI PMID:26310626 10199 Atm ataxia telangiectasia mutated gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:8917548 10199 Atm ataxia telangiectasia mutated gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20150806 MGI PMID:25683718 10199 Atm ataxia telangiectasia mutated gene MP:0005331 insulin resistance IAGP N RGD:5509061 20150806 MGI PMID:25683718 10199 Atm ataxia telangiectasia mutated gene MP:0005425 increased macrophage cell number IEA N RGD:5509061 20190418 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20150806 MGI PMID:25683718 10199 Atm ataxia telangiectasia mutated gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20170209 MGI PMID:26158450 10199 Atm ataxia telangiectasia mutated gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12195425 10199 Atm ataxia telangiectasia mutated gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20180125 MGI PMID:26310626 10199 Atm ataxia telangiectasia mutated gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15122331 10199 Atm ataxia telangiectasia mutated gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8917548 10199 Atm ataxia telangiectasia mutated gene MP:0008076 abnormal CD4-positive T cell differentiation IEA N RGD:5509061 20190613 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15122331 10199 Atm ataxia telangiectasia mutated gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20190418 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11389091 10199 Atm ataxia telangiectasia mutated gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20180125 MGI PMID:26310626 10199 Atm ataxia telangiectasia mutated gene MP:0008167 increased B-1a cell number IEA N RGD:5509061 20190418 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0008658 decreased interleukin-1 beta secretion IEA N RGD:5509061 20190418 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20150806 MGI PMID:25683718 10199 Atm ataxia telangiectasia mutated gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:18599436 10199 Atm ataxia telangiectasia mutated gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:22869596 10199 Atm ataxia telangiectasia mutated gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20180125 MGI PMID:26310626 10199 Atm ataxia telangiectasia mutated gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20161027 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0009021 absent estrus IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20170413 MGI PMID:27798842 10199 Atm ataxia telangiectasia mutated gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20194434 10199 Atm ataxia telangiectasia mutated gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20150212 MGI PMID:24532689 10199 Atm ataxia telangiectasia mutated gene MP:0010183 abnormal CD4-positive helper T cell morphology IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15122331 10199 Atm ataxia telangiectasia mutated gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12195425 10199 Atm ataxia telangiectasia mutated gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24709420 10199 Atm ataxia telangiectasia mutated gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20180125 MGI PMID:26310626 10199 Atm ataxia telangiectasia mutated gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20190613 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190613 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11040211 10199 Atm ataxia telangiectasia mutated gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16777961 10199 Atm ataxia telangiectasia mutated gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11967151 10199 Atm ataxia telangiectasia mutated gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22869596 10199 Atm ataxia telangiectasia mutated gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16777961 10199 Atm ataxia telangiectasia mutated gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18599436 10199 Atm ataxia telangiectasia mutated gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20826531 10199 Atm ataxia telangiectasia mutated gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20150806 MGI PMID:25683718 10199 Atm ataxia telangiectasia mutated gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:8689683 10199 Atm ataxia telangiectasia mutated gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:8843193 10199 Atm ataxia telangiectasia mutated gene MP:0011939 increased food intake IAGP N RGD:5509061 20150806 MGI PMID:25683718 10199 Atm ataxia telangiectasia mutated gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12195425 10199 Atm ataxia telangiectasia mutated gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16357220 10199 Atm ataxia telangiectasia mutated gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9582124 10199 Atm ataxia telangiectasia mutated gene MP:0012556 increased cell death IAGP N RGD:5509061 20150212 MGI PMID:18599436 10199 Atm ataxia telangiectasia mutated gene MP:0013236 ovary degeneration IAGP N RGD:5509061 20141120 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0014127 increased thymoma incidence IAGP N RGD:5509061 20160317 MGI PMID:8917548 10199 Atm ataxia telangiectasia mutated gene MP:0014127 increased thymoma incidence IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20161013 MGI PMID:26290337 10199 Atm ataxia telangiectasia mutated gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:8843194 10199 Atm ataxia telangiectasia mutated gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:10716718 10199 Atm ataxia telangiectasia mutated gene MP:0014378 increased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20181011 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20181011 MGI 10199 Atm ataxia telangiectasia mutated gene MP:0021001 impaired neuron physiology IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0021009 abnormal synaptic physiology IAGP N RGD:5509061 20220106 MGI PMID:34723800 10199 Atm ataxia telangiectasia mutated gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:25683718 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0000738 impaired muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11507009 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230119 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230119 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20111116 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20111116 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:17234593 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20231207 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230119 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20230119 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:17234593 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10360172 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0005333 decreased heart rate IEA N RGD:5509061 20230601 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20240523 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15485817 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:17234593 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20230119 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10360172 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20240523 MGI 10203 Atp1a1 ATPase, Na+/K+ transporting, alpha 1 polypeptide gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20240523 MGI 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21856916 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20141003 MGI PMID:12805306 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0001260 increased body weight IAGP N RGD:5509061 20190627 MGI PMID:26911348 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20190627 MGI PMID:26911348 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17234593 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20210826 MGI PMID:21731499 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190627 MGI PMID:26911348 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:15564586 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190627 MGI PMID:26911348 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20210826 MGI PMID:21731499 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20190627 MGI PMID:26911348 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17234593 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20190627 MGI PMID:26911348 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:15564586 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21856916 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:15564586 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20141003 MGI PMID:12805306 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15564586 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0002204 abnormal synaptic neurotransmitter level IAGP N RGD:5509061 20141003 MGI PMID:15564586 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15564586 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20190627 MGI PMID:26911348 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20210826 MGI PMID:21731499 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20190627 MGI PMID:26911348 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0002573 behavioral despair IAGP N RGD:5509061 20190627 MGI PMID:26911348 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21856916 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14559919 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20210826 MGI PMID:21731499 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10360172 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0005267 abnormal olfactory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12805306 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:15564586 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0005423 abnormal somatic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15564586 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15485817 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11507009 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0009710 anhedonia IAGP N RGD:5509061 20190627 MGI PMID:26911348 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20190627 MGI PMID:26911348 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10360172 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12805306 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15564586 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20190627 MGI PMID:26911348 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20210826 MGI PMID:21731499 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0012006 abnormal hippocampus physiology IAGP N RGD:5509061 20190627 MGI PMID:26911348 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0013140 excessive vocalization IAGP N RGD:5509061 20190627 MGI PMID:26911348 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0030732 increased gamma-aminobutyric acid level IAGP N RGD:5509061 20180927 MGI PMID:15564586 10206 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide gene MP:0030736 increased glutamic acid level IAGP N RGD:5509061 20190627 MGI PMID:26911348 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0000745 tremors IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0000801 abnormal temporal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:19666602 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20180712 MGI PMID:27549929 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:19666602 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19666602 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180712 MGI PMID:26463346 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19666602 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201231 MGI 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001393 ataxia IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17234593 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23652595 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001399 hyperactivity IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001399 hyperactivity IAGP N RGD:5509061 20180712 MGI PMID:27549929 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180712 MGI PMID:26463346 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001406 abnormal gait IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001407 short stride length IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001407 short stride length IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17234593 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001513 limb grasping IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001513 limb grasping IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0002064 seizures IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0002064 seizures IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19666602 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:23652595 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20141003 MGI PMID:23652595 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0002634 abnormal sensorimotor gating IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20180712 MGI PMID:26463346 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0002801 abnormal long-term object recognition memory IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0002801 abnormal long-term object recognition memory IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20180712 MGI PMID:27549929 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:19666602 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:23652595 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20180712 MGI PMID:27549929 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20180712 MGI PMID:26463346 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20180712 MGI PMID:27549929 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:23652595 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0005323 dystonia IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0005323 dystonia IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20180712 MGI PMID:27549929 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:19666602 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:23652595 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:19666602 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0009357 abnormal seizure response to inducing agent IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0009357 abnormal seizure response to inducing agent IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:19666602 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20180712 MGI PMID:26463346 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0009713 enhanced conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:17234593 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20180712 MGI PMID:27549929 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20180712 MGI PMID:27549929 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19666602 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17234593 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19666602 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23652595 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180712 MGI PMID:27549929 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180712 MGI PMID:27549929 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0011617 abnormal habituation IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20180712 MGI PMID:27549929 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0011624 abnormal sensitization to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0012286 decreased frequency of paradoxical sleep IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0012288 abnormal paradoxical sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0012289 abnormal non-rapid eye movement sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20180712 MGI PMID:27549929 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:23652595 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0020424 increased kindling response IAGP N RGD:5509061 20180712 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0020424 increased kindling response IAGP N RGD:5509061 20180920 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:22025725 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0031201 hemiparesis IAGP N RGD:5509061 20210218 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0031202 hemiplegia IAGP N RGD:5509061 20210218 MGI PMID:25523819 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0031202 hemiplegia IAGP N RGD:5509061 20210218 MGI PMID:30071271 10207 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22025725 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0000756 forelimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:9801359 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9801359 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:8793730 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:9801359 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:9801359 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:9801359 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:9801359 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:9801359 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7525597 10208 Atp1b2 ATPase, Na+/K+ transporting, beta 2 polypeptide gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:9801359 10209 Atp1b3 ATPase, Na+/K+ transporting, beta 3 polypeptide gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 10209 Atp1b3 ATPase, Na+/K+ transporting, beta 3 polypeptide gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20200402 MGI 10209 Atp1b3 ATPase, Na+/K+ transporting, beta 3 polypeptide gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20200402 MGI 10209 Atp1b3 ATPase, Na+/K+ transporting, beta 3 polypeptide gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20200402 MGI 10209 Atp1b3 ATPase, Na+/K+ transporting, beta 3 polypeptide gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20200402 MGI 10209 Atp1b3 ATPase, Na+/K+ transporting, beta 3 polypeptide gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20200402 MGI 10209 Atp1b3 ATPase, Na+/K+ transporting, beta 3 polypeptide gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220811 MGI 10209 Atp1b3 ATPase, Na+/K+ transporting, beta 3 polypeptide gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20200402 MGI 10209 Atp1b3 ATPase, Na+/K+ transporting, beta 3 polypeptide gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 10209 Atp1b3 ATPase, Na+/K+ transporting, beta 3 polypeptide gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 10209 Atp1b3 ATPase, Na+/K+ transporting, beta 3 polypeptide gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220811 MGI 10210 Atp2a3 ATPase, Ca++ transporting, ubiquitous gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9374548 10210 Atp2a3 ATPase, Ca++ transporting, ubiquitous gene MP:0004036 abnormal muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:9374548 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000032 cochlear degeneration IAGP N RGD:5509061 20141003 MGI PMID:10441500 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000032 cochlear degeneration IAGP N RGD:5509061 20141003 MGI PMID:10687933 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:21325754 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:21325754 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:16880690 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16880690 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9325047 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16529873 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:16880690 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000879 increased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16880690 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21325754 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20826782 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16880690 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20826782 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21325754 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9325047 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001394 circling IAGP N RGD:5509061 20151126 MGI PMID:23792079 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20151126 MGI PMID:23792079 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20826782 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9325047 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20151126 MGI PMID:23792079 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:9325047 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:23826306 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001490 abnormal vibrissae reflex IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:16880690 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16880690 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:21325754 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20151126 MGI PMID:23792079 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:16235133 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20151126 MGI PMID:23792079 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:16880690 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:21325754 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20151126 MGI PMID:23792079 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:9325047 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:16235133 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20151126 MGI PMID:23792079 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:10441500 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:10687933 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11124466 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:16529873 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:20826782 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:9325047 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001967 deafness IAGP N RGD:5509061 20151126 MGI PMID:23792079 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0001993 abnormal blinking IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11875276 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:10687933 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:11875276 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:21325754 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0002980 abnormal postural reflex IEA N RGD:5509061 20111116 MGI 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0003151 absent tunnel of Corti IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20141003 MGI PMID:7683393 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16529873 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17234811 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004301 absent organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004312 absent pillar cells IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004325 absent vestibular hair cells IAGP N RGD:5509061 20141003 MGI PMID:21325754 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004329 vestibular saccular degeneration IAGP N RGD:5509061 20141003 MGI PMID:10441500 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11875276 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:23826306 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10687933 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11875276 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21325754 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004408 decreased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004412 abnormal cochlear microphonics IAGP N RGD:5509061 20141003 MGI PMID:11124466 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004415 abnormal cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:11124466 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20141003 MGI PMID:17234811 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004432 abnormal cochlear hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17234811 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004438 abnormal vestibular hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17234811 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004438 abnormal vestibular hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004497 decreased organ of Corti supporting cell number IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20151126 MGI PMID:23792079 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:21325754 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004530 absent outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:11875276 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004586 pillar cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004597 increased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20141003 MGI PMID:11950541 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004631 abnormal auditory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16529873 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004716 abnormal cochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:11124466 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:11124466 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:16529873 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16529873 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:11950541 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:9325047 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004750 syndromic hearing loss IEA N RGD:5509061 20141003 MGI 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0004814 reduced linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:9325047 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0005307 head tossing IAGP N RGD:5509061 20151126 MGI PMID:23792079 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:10687933 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:21325754 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:21325754 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:23826306 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0008579 abnormal Purkinje cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7683393 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16845470 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:11124466 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:10687933 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11124466 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11950541 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18974863 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20826782 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21325754 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23826306 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:9325047 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:9668038 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0011968 decreased threshold for auditory brainstem response IAGP N RGD:5509061 20151126 MGI PMID:23792079 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0012490 abnormal cochlear VIII nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11875276 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:11124466 10211 Atp2b2 ATPase, Ca++ transporting, plasma membrane 2 gene MP:0014409 decreased distortion product otoacoustic emission amplitude IAGP N RGD:5509061 20240405 MGI PMID:11124466 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20180802 MGI PMID:27491072 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0001577 anemia IAGP N RGD:5509061 20180802 MGI PMID:27491072 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0003892 abnormal gastric gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10764766 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0003892 abnormal gastric gland morphology IAGP N RGD:5509061 20180802 MGI PMID:27491072 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10764766 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20180802 MGI PMID:27491072 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10764766 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0004731 increased circulating gastrin level IAGP N RGD:5509061 20141003 MGI PMID:10764766 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0004731 increased circulating gastrin level IAGP N RGD:5509061 20180802 MGI PMID:27491072 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0005213 gastric metaplasia IAGP N RGD:5509061 20141003 MGI PMID:10764766 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0005213 gastric metaplasia IAGP N RGD:5509061 20180802 MGI PMID:27491072 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0008003 achlorhydria IAGP N RGD:5509061 20141003 MGI PMID:10764766 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0008003 achlorhydria IAGP N RGD:5509061 20180802 MGI PMID:27491072 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20180802 MGI PMID:27491072 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0008387 hypochromic anemia IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0010783 abnormal stomach wall morphology IAGP N RGD:5509061 20180802 MGI PMID:27491072 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0010787 gastric cyst IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0010787 gastric cyst IAGP N RGD:5509061 20180802 MGI PMID:27491072 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20180802 MGI PMID:27491072 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0010803 abnormal stomach enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10764766 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:21976678 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0011891 decreased circulating ferritin level IAGP N RGD:5509061 20180802 MGI PMID:27491072 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0013566 dilated gastric gland IAGP N RGD:5509061 20150312 MGI PMID:10764766 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0013578 abnormal stomach glandular region morphology IAGP N RGD:5509061 20180802 MGI PMID:27491072 10212 Atp4a ATPase, H+/K+ exchanging, gastric, alpha polypeptide gene MP:0031084 decreased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:21976678 10213 Atp4b ATPase, H+/K+ exchanging, beta polypeptide gene MP:0003892 abnormal gastric gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10464136 10213 Atp4b ATPase, H+/K+ exchanging, beta polypeptide gene MP:0003892 abnormal gastric gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11705756 10213 Atp4b ATPase, H+/K+ exchanging, beta polypeptide gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10464136 10213 Atp4b ATPase, H+/K+ exchanging, beta polypeptide gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11705756 10213 Atp4b ATPase, H+/K+ exchanging, beta polypeptide gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20150312 MGI PMID:10464136 10213 Atp4b ATPase, H+/K+ exchanging, beta polypeptide gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20150312 MGI PMID:11705756 10213 Atp4b ATPase, H+/K+ exchanging, beta polypeptide gene MP:0004731 increased circulating gastrin level IAGP N RGD:5509061 20141003 MGI PMID:10464136 10213 Atp4b ATPase, H+/K+ exchanging, beta polypeptide gene MP:0005211 increased stomach mucosa thickness IAGP N RGD:5509061 20141003 MGI PMID:10464136 10213 Atp4b ATPase, H+/K+ exchanging, beta polypeptide gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20141003 MGI PMID:10464136 10213 Atp4b ATPase, H+/K+ exchanging, beta polypeptide gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10464136 10213 Atp4b ATPase, H+/K+ exchanging, beta polypeptide gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:11705756 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20151203 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:8895222 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:1115218 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:3385878 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:4808708 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20889 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:3385878 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:4858102 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000372 irregular coat pigmentation IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000400 abnormal awl hair morphology IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000402 abnormal zigzag hair morphology IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000410 waved hair IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000421 mottled coat IAGP N RGD:5509061 20141003 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000421 mottled coat IAGP N RGD:5509061 20141003 MGI PMID:8640230 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000489 abnormal large intestine morphology IEA N RGD:5509061 20190801 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000576 clubfoot IEA N RGD:5509061 20151203 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20831904 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:4858102 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:8640230 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:20831904 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20190808 MGI PMID:25639447 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20190808 MGI PMID:25639447 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:4808708 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001263 weight loss IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8640230 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:11386751 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:13103353 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:22900086 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:9166584 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20151203 MGI PMID:25456742 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001278 kinked vibrissae IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001279 wavy vibrissae IAGP N RGD:5509061 20190808 MGI PMID:7130053 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001284 absent vibrissae IEA N RGD:5509061 20120209 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20831904 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9166584 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:4858102 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190808 MGI PMID:25639447 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:8640230 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001406 abnormal gait IAGP N RGD:5509061 20190808 MGI PMID:25639447 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:1115218 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20141003 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001513 limb grasping IAGP N RGD:5509061 20190808 MGI PMID:25639447 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001524 impaired limb coordination IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001525 impaired balance IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22900086 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:22900086 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:9166584 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20190801 MGI PMID:1819648 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20190801 MGI PMID:6685755 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001926 female infertility IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001935 decreased litter size IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:937819 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20190808 MGI PMID:25639447 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002074 abnormal hair texture IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:13103353 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:22869751 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8640230 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8672124 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8640230 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9147645 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9147646 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9147646 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002115 abnormal limb bone morphology IEA N RGD:5509061 20111222 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:937819 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8640230 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20190808 MGI PMID:25639447 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:937819 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11534785 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:9166584 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002832 coarse hair IAGP N RGD:5509061 20141003 MGI PMID:1115218 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0002861 abnormal tail bud morphology IAGP N RGD:5509061 20141003 MGI PMID:22900086 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003067 decreased liver copper level IAGP N RGD:5509061 20141003 MGI PMID:20831904 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003067 decreased liver copper level IAGP N RGD:5509061 20141003 MGI PMID:8640230 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003067 decreased liver copper level IAGP N RGD:5509061 20190801 MGI PMID:1819648 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003067 decreased liver copper level IAGP N RGD:5509061 20190801 MGI PMID:6685755 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003067 decreased liver copper level IAGP N RGD:5509061 20240912 MGI PMID:4858102 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200402 MGI PMID:27293072 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:4808708 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003198 calcified tendon IEA N RGD:5509061 20181004 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19375486 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:1115218 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:4808708 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003279 aneurysm IAGP N RGD:5509061 20141003 MGI PMID:1115218 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003415 priapism IAGP N RGD:5509061 20141003 MGI PMID:1115218 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:8895222 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:16371425 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:22900086 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20190808 MGI PMID:7130053 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003907 decreased aorta elastin content IAGP N RGD:5509061 20141003 MGI PMID:1115218 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:11534785 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003951 abnormal copper homeostasis IAGP N RGD:5509061 20190801 MGI PMID:6685755 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003952 abnormal copper level IAGP N RGD:5509061 20141003 MGI PMID:20831904 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003952 abnormal copper level IAGP N RGD:5509061 20190808 MGI PMID:25639447 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003952 abnormal copper level IAGP N RGD:5509061 20200402 MGI PMID:27293072 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:4858102 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0004043 abnormal pH regulation IAGP N RGD:5509061 20190808 MGI PMID:9342151 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:11534785 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0004508 abnormal pectoral girdle bone morphology IEA N RGD:5509061 20151203 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20151203 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0004676 wide ribs IEA N RGD:5509061 20151203 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20190808 MGI PMID:25639447 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0004882 enlarged lung IAGP N RGD:5509061 20141003 MGI PMID:937819 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20190801 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:1115218 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:22869751 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:1115218 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:1115218 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20190808 MGI PMID:25639447 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:22869751 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005366 variegated coat color IAGP N RGD:5509061 20141003 MGI PMID:11386751 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005366 variegated coat color IAGP N RGD:5509061 20151203 MGI PMID:25456742 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:22900086 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:1115218 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005508 abnormal skeleton morphology IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16371425 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:20889 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20151203 MGI PMID:25456742 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20190808 MGI PMID:10098864 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20190808 MGI PMID:9342151 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200402 MGI PMID:27293072 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20190808 MGI PMID:9342151 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20151203 MGI PMID:25456742 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:1115218 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:3385878 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:4808708 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0006349 decreased circulating copper level IAGP N RGD:5509061 20141003 MGI PMID:4858102 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:4808708 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0008731 abnormal hair shaft melanin granule morphology IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:8640230 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20200402 MGI PMID:27293072 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:22900086 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010016 variable depigmentation IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20190808 MGI PMID:25639447 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010062 decreased creatine level IAGP N RGD:5509061 20190808 MGI PMID:9342151 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010243 increased kidney copper level IAGP N RGD:5509061 20141003 MGI PMID:11534785 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010243 increased kidney copper level IAGP N RGD:5509061 20141003 MGI PMID:20831904 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010243 increased kidney copper level IAGP N RGD:5509061 20190801 MGI PMID:6685755 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010247 increased intestine copper level IAGP N RGD:5509061 20141003 MGI PMID:4858102 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010247 increased intestine copper level IAGP N RGD:5509061 20141003 MGI PMID:8640230 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010247 increased intestine copper level IAGP N RGD:5509061 20190801 MGI PMID:6685755 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010247 increased intestine copper level IAGP N RGD:5509061 20190808 MGI PMID:7333461 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010389 mosaic coat color IAGP N RGD:5509061 20141003 MGI PMID:22869751 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010470 dilated ascending aorta IAGP N RGD:5509061 20141003 MGI PMID:3385878 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010574 dilated aorta IAGP N RGD:5509061 20141003 MGI PMID:1115218 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010769 abnormal survival IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:937819 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:937819 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20141003 MGI PMID:937819 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010908 dilated pulmonary alveolar duct IAGP N RGD:5509061 20141003 MGI PMID:937819 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0010937 increased total lung capacity IAGP N RGD:5509061 20141003 MGI PMID:937819 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22869751 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8640230 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9147646 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22900086 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011089 perinatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011090 perinatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11386751 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22869751 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22900086 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9147646 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8640230 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:13103353 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22869751 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22900086 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8640230 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IEA N RGD:5509061 20151203 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011214 increased brain copper level IAGP N RGD:5509061 20200402 MGI PMID:27293072 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011215 decreased brain copper level IAGP N RGD:5509061 20141003 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011215 decreased brain copper level IAGP N RGD:5509061 20141003 MGI PMID:20831904 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011215 decreased brain copper level IAGP N RGD:5509061 20141003 MGI PMID:22869751 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011215 decreased brain copper level IAGP N RGD:5509061 20141003 MGI PMID:4858102 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011215 decreased brain copper level IAGP N RGD:5509061 20151203 MGI PMID:25456742 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011215 decreased brain copper level IAGP N RGD:5509061 20190801 MGI PMID:6685755 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0011218 decreased brainstem copper level IEA N RGD:5509061 20190801 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20151203 MGI PMID:25456742 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20240912 MGI PMID:4858102 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0012661 decreased circulating ceruloplasmin level IEA N RGD:5509061 20141003 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20160428 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0014539 increased copper level IAGP N RGD:5509061 20240912 MGI PMID:16338116 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0014540 decreased copper level IEA N RGD:5509061 20240912 MGI 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0020308 decreased creatine kinase activity IAGP N RGD:5509061 20190808 MGI PMID:9342151 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0031200 increased aortic weight IAGP N RGD:5509061 20201119 MGI PMID:4808708 10215 Atp7a ATPase, copper transporting, alpha polypeptide gene MP:0031204 hindlimb paresis IEA N RGD:5509061 20210218 MGI 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:6863890 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:10441329 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:14617772 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17981064 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8040371 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10441329 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:6863890 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0000794 abnormal parietal lobe morphology IEA N RGD:5509061 20111116 MGI 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0000798 abnormal frontal lobe morphology IEA N RGD:5509061 20111116 MGI 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0000804 abnormal occipital lobe morphology IEA N RGD:5509061 20111116 MGI 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:6863890 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:6863890 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:10441329 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10441329 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:6863890 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:6863890 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0001569 abnormal circulating bilirubin level IEA N RGD:5509061 20180215 MGI 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10441329 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:6863890 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0001881 abnormal mammary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:10441329 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:6863890 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:6863890 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:6863890 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20111116 MGI 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0003046 liver cirrhosis IAGP N RGD:5509061 20141003 MGI PMID:10441329 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0003046 liver cirrhosis IAGP N RGD:5509061 20141003 MGI PMID:2845190 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0003065 abnormal liver copper level IAGP N RGD:5509061 20141003 MGI PMID:10441329 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0003066 increased liver copper level IAGP N RGD:5509061 20141003 MGI PMID:2845190 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0003066 increased liver copper level IAGP N RGD:5509061 20141003 MGI PMID:6863890 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0003066 increased liver copper level IAGP N RGD:5509061 20141003 MGI PMID:8040371 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0003067 decreased liver copper level IAGP N RGD:5509061 20141003 MGI PMID:6863890 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0003224 neuron degeneration IEA N RGD:5509061 20111116 MGI 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:14617772 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:11085952 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0003952 abnormal copper level IAGP N RGD:5509061 20141003 MGI PMID:10441329 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0003952 abnormal copper level IAGP N RGD:5509061 20141003 MGI PMID:8040371 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20111116 MGI 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:6863890 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0006349 decreased circulating copper level IAGP N RGD:5509061 20141003 MGI PMID:6863890 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0006350 increased circulating copper level IAGP N RGD:5509061 20141003 MGI PMID:8040371 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0008540 abnormal cerebral hemisphere morphology IEA N RGD:5509061 20111116 MGI 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0009618 increased brain zinc level IAGP N RGD:5509061 20240912 MGI PMID:8040371 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0010243 increased kidney copper level IAGP N RGD:5509061 20141003 MGI PMID:8040371 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6863890 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10441329 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0011214 increased brain copper level IAGP N RGD:5509061 20141003 MGI PMID:14617772 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0011214 increased brain copper level IAGP N RGD:5509061 20141003 MGI PMID:8040371 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0014539 increased copper level IAGP N RGD:5509061 20240912 MGI PMID:14617772 10217 Atp7b ATPase, copper transporting, beta polypeptide gene MP:0014549 increased zinc level IAGP N RGD:5509061 20240912 MGI PMID:8040371 10220 Avp arginine vasopressin gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20181227 MGI 10220 Avp arginine vasopressin gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:14660745 10220 Avp arginine vasopressin gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:19297548 10220 Avp arginine vasopressin gene MP:0001523 impaired righting response IEA N RGD:5509061 20160421 MGI 10220 Avp arginine vasopressin gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:14660745 10220 Avp arginine vasopressin gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:19297548 10220 Avp arginine vasopressin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14660745 10220 Avp arginine vasopressin gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:19297548 10220 Avp arginine vasopressin gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:19297548 10220 Avp arginine vasopressin gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 10220 Avp arginine vasopressin gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:14660745 10220 Avp arginine vasopressin gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20201022 MGI 10220 Avp arginine vasopressin gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20141003 MGI PMID:14660745 10220 Avp arginine vasopressin gene MP:0008846 abnormal supraoptic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19297548 10220 Avp arginine vasopressin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14660745 10220 Avp arginine vasopressin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19297548 10220 Avp arginine vasopressin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180510 MGI PMID:26342201 10220 Avp arginine vasopressin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10220 Avp arginine vasopressin gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:14660745 10220 Avp arginine vasopressin gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:19297548 10220 Avp arginine vasopressin gene MP:0012361 decreased large unstained cell number IEA N RGD:5509061 20181227 MGI 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11104789 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:11104789 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20220616 MGI PMID:19729836 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11104789 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220616 MGI PMID:19729836 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:11104789 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0001426 polydipsia IAGP N RGD:5509061 20220616 MGI PMID:19729836 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:11104789 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20220616 MGI PMID:19729836 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:11104789 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11104789 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:11104789 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20220616 MGI PMID:19729836 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:11104789 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:11104789 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20220616 MGI PMID:19729836 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20220616 MGI PMID:19729836 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0005633 increased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:11104789 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20220616 MGI PMID:19729836 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11104789 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0011467 decreased urine urea nitrogen level IAGP N RGD:5509061 20220616 MGI PMID:19729836 10222 Avpr2 arginine vasopressin receptor 2 gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20220616 MGI PMID:19729836 10223 Azgp1 alpha-2-glycoprotein 1, zinc gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17234189 10223 Azgp1 alpha-2-glycoprotein 1, zinc gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17234189 10223 Azgp1 alpha-2-glycoprotein 1, zinc gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:17234189 10223 Azgp1 alpha-2-glycoprotein 1, zinc gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:17234189 10224 B2m beta-2 microglobulin gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:7930593 10224 B2m beta-2 microglobulin gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:9741021 10224 B2m beta-2 microglobulin gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:12065839 10224 B2m beta-2 microglobulin gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7930593 10224 B2m beta-2 microglobulin gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7930593 10224 B2m beta-2 microglobulin gene MP:0000726 absent lymphocyte IAGP N RGD:5509061 20141003 MGI PMID:9103418 10224 B2m beta-2 microglobulin gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:12065839 10224 B2m beta-2 microglobulin gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:16493087 10224 B2m beta-2 microglobulin gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:18198358 10224 B2m beta-2 microglobulin gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:2112266 10224 B2m beta-2 microglobulin gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20230316 MGI PMID:30295892 10224 B2m beta-2 microglobulin gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20210422 MGI 10224 B2m beta-2 microglobulin gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:11114377 10224 B2m beta-2 microglobulin gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:7930593 10224 B2m beta-2 microglobulin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7930593 10224 B2m beta-2 microglobulin gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:11118151 10224 B2m beta-2 microglobulin gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 10224 B2m beta-2 microglobulin gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7930593 10224 B2m beta-2 microglobulin gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9103418 10224 B2m beta-2 microglobulin gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12566415 10224 B2m beta-2 microglobulin gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9103418 10224 B2m beta-2 microglobulin gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:2112266 10224 B2m beta-2 microglobulin gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:9103418 10224 B2m beta-2 microglobulin gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:11118151 10224 B2m beta-2 microglobulin gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:18198358 10224 B2m beta-2 microglobulin gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9103418 10224 B2m beta-2 microglobulin gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210422 MGI 10224 B2m beta-2 microglobulin gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12750472 10224 B2m beta-2 microglobulin gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15446308 10224 B2m beta-2 microglobulin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9103418 10224 B2m beta-2 microglobulin gene MP:0002083 premature death IAGP N RGD:5509061 20180111 MGI PMID:21964024 10224 B2m beta-2 microglobulin gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11687799 10224 B2m beta-2 microglobulin gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20360383 10224 B2m beta-2 microglobulin gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:7930593 10224 B2m beta-2 microglobulin gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18776905 10224 B2m beta-2 microglobulin gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17562770 10224 B2m beta-2 microglobulin gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:16493087 10224 B2m beta-2 microglobulin gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:2139497 10224 B2m beta-2 microglobulin gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7589135 10224 B2m beta-2 microglobulin gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22036949 10224 B2m beta-2 microglobulin gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:7930593 10224 B2m beta-2 microglobulin gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:7930593 10224 B2m beta-2 microglobulin gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12566415 10224 B2m beta-2 microglobulin gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:7930593 10224 B2m beta-2 microglobulin gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:7930593 10224 B2m beta-2 microglobulin gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:7589135 10224 B2m beta-2 microglobulin gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:9741021 10224 B2m beta-2 microglobulin gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9741021 10224 B2m beta-2 microglobulin gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11118151 10224 B2m beta-2 microglobulin gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:12486099 10224 B2m beta-2 microglobulin gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:12065839 10224 B2m beta-2 microglobulin gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:16751419 10224 B2m beta-2 microglobulin gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:20360383 10224 B2m beta-2 microglobulin gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:8258349 10224 B2m beta-2 microglobulin gene MP:0004165 abnormal lateral geniculate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11118151 10224 B2m beta-2 microglobulin gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16493087 10224 B2m beta-2 microglobulin gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17420446 10224 B2m beta-2 microglobulin gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:17420446 10224 B2m beta-2 microglobulin gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20180111 MGI PMID:21964024 10224 B2m beta-2 microglobulin gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20171214 MGI PMID:21964024 10224 B2m beta-2 microglobulin gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:12361980 10224 B2m beta-2 microglobulin gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:16493087 10224 B2m beta-2 microglobulin gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10725754 10224 B2m beta-2 microglobulin gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:11572996 10224 B2m beta-2 microglobulin gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:15446308 10224 B2m beta-2 microglobulin gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:16493087 10224 B2m beta-2 microglobulin gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:18198358 10224 B2m beta-2 microglobulin gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:8314025 10224 B2m beta-2 microglobulin gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20160218 MGI PMID:12361980 10224 B2m beta-2 microglobulin gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10725754 10224 B2m beta-2 microglobulin gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22561606 10224 B2m beta-2 microglobulin gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9741021 10224 B2m beta-2 microglobulin gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9164958 10224 B2m beta-2 microglobulin gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:7589135 10224 B2m beta-2 microglobulin gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:9741021 10224 B2m beta-2 microglobulin gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16493087 10224 B2m beta-2 microglobulin gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:2139497 10224 B2m beta-2 microglobulin gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:7589135 10224 B2m beta-2 microglobulin gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:9741021 10224 B2m beta-2 microglobulin gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8314025 10224 B2m beta-2 microglobulin gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20360383 10224 B2m beta-2 microglobulin gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:12566415 10224 B2m beta-2 microglobulin gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:9103418 10224 B2m beta-2 microglobulin gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9741021 10224 B2m beta-2 microglobulin gene MP:0005638 hemochromatosis IAGP N RGD:5509061 20141003 MGI PMID:8013958 10224 B2m beta-2 microglobulin gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:9103418 10224 B2m beta-2 microglobulin gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:12634786 10224 B2m beta-2 microglobulin gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:9075933 10224 B2m beta-2 microglobulin gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:7930593 10224 B2m beta-2 microglobulin gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20360383 10224 B2m beta-2 microglobulin gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7589135 10224 B2m beta-2 microglobulin gene MP:0008077 abnormal CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18195075 10224 B2m beta-2 microglobulin gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20360383 10224 B2m beta-2 microglobulin gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23315079 10224 B2m beta-2 microglobulin gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8898201 10224 B2m beta-2 microglobulin gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9551897 10224 B2m beta-2 microglobulin gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1346234 10224 B2m beta-2 microglobulin gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16493087 10224 B2m beta-2 microglobulin gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17562770 10224 B2m beta-2 microglobulin gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19721454 10224 B2m beta-2 microglobulin gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:2112266 10224 B2m beta-2 microglobulin gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:2139497 10224 B2m beta-2 microglobulin gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23109710 10224 B2m beta-2 microglobulin gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9182675 10224 B2m beta-2 microglobulin gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18776905 10224 B2m beta-2 microglobulin gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19597498 10224 B2m beta-2 microglobulin gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:15446308 10224 B2m beta-2 microglobulin gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:17562770 10224 B2m beta-2 microglobulin gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:7930593 10224 B2m beta-2 microglobulin gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8898201 10224 B2m beta-2 microglobulin gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1346234 10224 B2m beta-2 microglobulin gene MP:0008350 increased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:1346234 10224 B2m beta-2 microglobulin gene MP:0008401 abnormal CD8 positive, alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7589135 10224 B2m beta-2 microglobulin gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:11118151 10224 B2m beta-2 microglobulin gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:9164958 10224 B2m beta-2 microglobulin gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:17420446 10224 B2m beta-2 microglobulin gene MP:0008696 increased interleukin-3 secretion IAGP N RGD:5509061 20141003 MGI PMID:9164958 10224 B2m beta-2 microglobulin gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:9164958 10224 B2m beta-2 microglobulin gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:17562770 10224 B2m beta-2 microglobulin gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:7930593 10224 B2m beta-2 microglobulin gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17562770 10224 B2m beta-2 microglobulin gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:7930593 10224 B2m beta-2 microglobulin gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:10791995 10224 B2m beta-2 microglobulin gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:9103418 10224 B2m beta-2 microglobulin gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:17420446 10224 B2m beta-2 microglobulin gene MP:0009709 hydrometra IEA N RGD:5509061 20210422 MGI 10224 B2m beta-2 microglobulin gene MP:0009787 increased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17562770 10224 B2m beta-2 microglobulin gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:21179499 10224 B2m beta-2 microglobulin gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:16751419 10224 B2m beta-2 microglobulin gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9103418 10224 B2m beta-2 microglobulin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 10224 B2m beta-2 microglobulin gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12150996 10224 B2m beta-2 microglobulin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210422 MGI 10224 B2m beta-2 microglobulin gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 10225 Baat bile acid-Coenzyme A: amino acid N-acyltransferase gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 10225 Baat bile acid-Coenzyme A: amino acid N-acyltransferase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 10225 Baat bile acid-Coenzyme A: amino acid N-acyltransferase gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 10225 Baat bile acid-Coenzyme A: amino acid N-acyltransferase gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 10225 Baat bile acid-Coenzyme A: amino acid N-acyltransferase gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 10225 Baat bile acid-Coenzyme A: amino acid N-acyltransferase gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 10225 Baat bile acid-Coenzyme A: amino acid N-acyltransferase gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 10225 Baat bile acid-Coenzyme A: amino acid N-acyltransferase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 10225 Baat bile acid-Coenzyme A: amino acid N-acyltransferase gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 10225 Baat bile acid-Coenzyme A: amino acid N-acyltransferase gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 10226 Bax BCL2-associated X protein gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7569956 10226 Bax BCL2-associated X protein gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0000706 small thymus IAGP N RGD:5509061 20151112 MGI PMID:19706873 10226 Bax BCL2-associated X protein gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:7569956 10226 Bax BCL2-associated X protein gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20151112 MGI PMID:19706873 10226 Bax BCL2-associated X protein gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:22884324 10226 Bax BCL2-associated X protein gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:10804210 10226 Bax BCL2-associated X protein gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10804210 10226 Bax BCL2-associated X protein gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:10804210 10226 Bax BCL2-associated X protein gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10804210 10226 Bax BCL2-associated X protein gene MP:0000909 abnormal facial motor nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:8816704 10226 Bax BCL2-associated X protein gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16928866 10226 Bax BCL2-associated X protein gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:16928866 10226 Bax BCL2-associated X protein gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:16928866 10226 Bax BCL2-associated X protein gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12741988 10226 Bax BCL2-associated X protein gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15836427 10226 Bax BCL2-associated X protein gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:21151121 10226 Bax BCL2-associated X protein gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8816704 10226 Bax BCL2-associated X protein gene MP:0001025 abnormal sympathetic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8816704 10226 Bax BCL2-associated X protein gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12668632 10226 Bax BCL2-associated X protein gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20392943 10226 Bax BCL2-associated X protein gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12441053 10226 Bax BCL2-associated X protein gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20160804 MGI PMID:24453327 10226 Bax BCL2-associated X protein gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:10894153 10226 Bax BCL2-associated X protein gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:9988273 10226 Bax BCL2-associated X protein gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:16270031 10226 Bax BCL2-associated X protein gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:7569956 10226 Bax BCL2-associated X protein gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10894153 10226 Bax BCL2-associated X protein gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16270031 10226 Bax BCL2-associated X protein gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:16414041 10226 Bax BCL2-associated X protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15578095 10226 Bax BCL2-associated X protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16270031 10226 Bax BCL2-associated X protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15578095 10226 Bax BCL2-associated X protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22884324 10226 Bax BCL2-associated X protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20160331 MGI PMID:26203146 10226 Bax BCL2-associated X protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10804210 10226 Bax BCL2-associated X protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22117778 10226 Bax BCL2-associated X protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22884324 10226 Bax BCL2-associated X protein gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16928866 10226 Bax BCL2-associated X protein gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:15578095 10226 Bax BCL2-associated X protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10894153 10226 Bax BCL2-associated X protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16270031 10226 Bax BCL2-associated X protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:7569956 10226 Bax BCL2-associated X protein gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:18281459 10226 Bax BCL2-associated X protein gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:24036309 10226 Bax BCL2-associated X protein gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16928866 10226 Bax BCL2-associated X protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18288109 10226 Bax BCL2-associated X protein gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:15578095 10226 Bax BCL2-associated X protein gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:16928866 10226 Bax BCL2-associated X protein gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20200507 MGI PMID:28346224 10226 Bax BCL2-associated X protein gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16270031 10226 Bax BCL2-associated X protein gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:7569956 10226 Bax BCL2-associated X protein gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19755105 10226 Bax BCL2-associated X protein gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20141003 MGI PMID:17107997 10226 Bax BCL2-associated X protein gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20141003 MGI PMID:22216013 10226 Bax BCL2-associated X protein gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15578095 10226 Bax BCL2-associated X protein gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10744634 10226 Bax BCL2-associated X protein gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11150333 10226 Bax BCL2-associated X protein gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8816704 10226 Bax BCL2-associated X protein gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9096145 10226 Bax BCL2-associated X protein gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20141003 MGI PMID:22884324 10226 Bax BCL2-associated X protein gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:15836427 10226 Bax BCL2-associated X protein gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12741988 10226 Bax BCL2-associated X protein gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15247919 10226 Bax BCL2-associated X protein gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23522042 10226 Bax BCL2-associated X protein gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:15578095 10226 Bax BCL2-associated X protein gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16270031 10226 Bax BCL2-associated X protein gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10894153 10226 Bax BCL2-associated X protein gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23805138 10226 Bax BCL2-associated X protein gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:7569956 10226 Bax BCL2-associated X protein gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:10894153 10226 Bax BCL2-associated X protein gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:16270031 10226 Bax BCL2-associated X protein gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:18281459 10226 Bax BCL2-associated X protein gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:7569956 10226 Bax BCL2-associated X protein gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:8816704 10226 Bax BCL2-associated X protein gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0006006 increased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:15836427 10226 Bax BCL2-associated X protein gene MP:0006006 increased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:23522042 10226 Bax BCL2-associated X protein gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:16928866 10226 Bax BCL2-associated X protein gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11150333 10226 Bax BCL2-associated X protein gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0008206 increased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 10226 Bax BCL2-associated X protein gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:16270031 10226 Bax BCL2-associated X protein gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18281459 10226 Bax BCL2-associated X protein gene MP:0008390 abnormal primordial germ cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17107997 10226 Bax BCL2-associated X protein gene MP:0008391 abnormal primordial germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22216013 10226 Bax BCL2-associated X protein gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:22216013 10226 Bax BCL2-associated X protein gene MP:0008468 absent muscle spindles IAGP N RGD:5509061 20141003 MGI PMID:12741988 10226 Bax BCL2-associated X protein gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0008485 increased muscle spindle number IAGP N RGD:5509061 20141003 MGI PMID:15247919 10226 Bax BCL2-associated X protein gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:10804210 10226 Bax BCL2-associated X protein gene MP:0008870 increased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:9988273 10226 Bax BCL2-associated X protein gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:10804210 10226 Bax BCL2-associated X protein gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0009083 uterus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9988273 10226 Bax BCL2-associated X protein gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17676052 10226 Bax BCL2-associated X protein gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20151112 MGI PMID:19706873 10226 Bax BCL2-associated X protein gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:10804210 10226 Bax BCL2-associated X protein gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22884324 10226 Bax BCL2-associated X protein gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11163212 10226 Bax BCL2-associated X protein gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22884324 10226 Bax BCL2-associated X protein gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9096145 10226 Bax BCL2-associated X protein gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20160331 MGI PMID:26203146 10226 Bax BCL2-associated X protein gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16270031 10226 Bax BCL2-associated X protein gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20160804 MGI PMID:24453327 10226 Bax BCL2-associated X protein gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20180705 MGI PMID:27452460 10226 Bax BCL2-associated X protein gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:15578095 10226 Bax BCL2-associated X protein gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:7569956 10226 Bax BCL2-associated X protein gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:7569956 10227 Bcan brevican gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:12370289 10227 Bcan brevican gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12370289 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210128 MGI 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20181227 MGI 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0001260 increased body weight IAGP N RGD:5509061 20191017 MGI PMID:31435015 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0002981 increased liver weight IAGP N RGD:5509061 20191017 MGI PMID:31435015 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20240307 MGI PMID:33944778 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20191017 MGI PMID:31435015 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0005331 insulin resistance IAGP N RGD:5509061 20191017 MGI PMID:31435015 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20191017 MGI PMID:31435015 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20191017 MGI PMID:31435015 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20191017 MGI PMID:31435015 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20191017 MGI PMID:31435015 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200402 MGI 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20191017 MGI PMID:31435015 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20191017 MGI PMID:31435015 10228 Bckdha branched chain ketoacid dehydrogenase E1, alpha polypeptide gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20191017 MGI PMID:31435015 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22258505 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22258505 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19651893 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:19651893 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000372 irregular coat pigmentation IEA N RGD:5509061 20111116 MGI 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:7840250 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:8760259 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:8623928 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:8760259 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21606958 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21606958 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000909 abnormal facial motor nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:8755480 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:8755480 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:8755480 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8755480 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001025 abnormal sympathetic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8755480 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19651893 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14749373 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19651893 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8755480 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10321489 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22258505 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19651893 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21606958 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12414660 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12414660 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22258505 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14749373 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19651893 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21606958 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8755480 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20181206 MGI PMID:28806762 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16982684 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21606958 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:8623928 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15708569 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002955 increased compensatory renal growth IAGP N RGD:5509061 20141003 MGI PMID:8760259 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:7840250 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:8623928 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21606958 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7840250 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8623928 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8760259 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:9950951 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:7840250 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:19651893 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:14749373 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:8760259 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:9950951 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15708569 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:8760259 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:14749373 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:7840250 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:8623928 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:7628407 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:8623928 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19651893 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19651893 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0004969 pale kidney IAGP N RGD:5509061 20150702 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21606958 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16982684 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16982684 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22258505 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22258505 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22258505 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:8623928 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:18988889 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005457 abnormal percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:22258505 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:7840250 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:8755480 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:7840250 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:8755480 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22258505 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0006057 decreased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:15708569 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0006405 abnormal L3 dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8755480 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10321489 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20150702 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16982684 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21606958 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16982684 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21606958 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16982684 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:16982684 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:19651893 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:14749373 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:19651893 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:8755480 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:8760259 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16982684 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008961 abnormal basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:22258505 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0008962 abnormal carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:22258505 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0009051 dilated distal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0009051 dilated distal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0009317 increased follicular lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21606958 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0009322 increased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19651893 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0009341 decreased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19651893 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0009361 abnormal primordial ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:7628407 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:11146504 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:15708569 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20181122 MGI PMID:20144786 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0010979 small ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:8623928 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0010982 abnormal ureteric bud elongation IAGP N RGD:5509061 20141003 MGI PMID:8623928 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:7840250 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0010985 abnormal kidney mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:19651893 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18988889 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:7840250 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:8623928 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:8623928 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20141003 MGI PMID:8760259 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:7840250 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:8623928 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011365 small metanephros IAGP N RGD:5509061 20141003 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011365 small metanephros IAGP N RGD:5509061 20141003 MGI PMID:7840250 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8623928 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8760259 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011369 increased renal glomerulus apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011376 abnormal kidney corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:8623928 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:7840250 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011408 renal tubule hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:8623928 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011408 renal tubule hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011425 abnormal kidney interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8760259 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011457 abnormal metanephric ureteric bud development IAGP N RGD:5509061 20141003 MGI PMID:7840250 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011483 renal glomerular synechia IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011498 abnormal glomerular capsule parietal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011500 decreased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011502 parietal capsular epithelium metaplasia IAGP N RGD:5509061 20141003 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0011871 podocyte hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9794553 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:22258505 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20160310 MGI PMID:7812968 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0020084 short ears IAGP N RGD:5509061 20170914 MGI PMID:11709185 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0030188 round snout IAGP N RGD:5509061 20171019 MGI PMID:8402909 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0030188 round snout IAGP N RGD:5509061 20171109 MGI PMID:8170972 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:22258505 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0030967 abnormal circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:22258505 10230 Bcl2 B cell leukemia/lymphoma 2 gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:22258505 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16604193 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16604193 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12637363 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16604193 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16604193 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11015607 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:11015607 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:11015607 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12637363 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20141003 MGI PMID:12637363 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16604193 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17452647 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:12560214 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11956243 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7775424 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16604193 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11015607 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:11015607 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16604193 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0002829 abnormal juxtaglomerular apparatus morphology IAGP N RGD:5509061 20141003 MGI PMID:11015607 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:12637363 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:12637363 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12637363 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:11015607 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:12637363 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17452647 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11015607 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16497152 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:17452647 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17452647 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17452647 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12637363 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:16604193 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16497152 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16604193 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16497152 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11015607 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17452647 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0010145 abnormal spermatic cord morphology IAGP N RGD:5509061 20220324 MGI PMID:16604193 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11015607 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0011300 abnormal juxtaglomerular cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11015607 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:12560214 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0011347 abnormal kidney medullary ray morphology IAGP N RGD:5509061 20141003 MGI PMID:11015607 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:11015607 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0011638 abnormal mitochondrial chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:16604193 10232 Bdkrb2 bradykinin receptor, beta 2 gene MP:0011742 decreased urine nitrite level IAGP N RGD:5509061 20141003 MGI PMID:12560214 10235 Bdnf brain derived neurotrophic factor gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:9973328 10235 Bdnf brain derived neurotrophic factor gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:10363708 10235 Bdnf brain derived neurotrophic factor gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10514401 10235 Bdnf brain derived neurotrophic factor gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:10514401 10235 Bdnf brain derived neurotrophic factor gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:20130183 10235 Bdnf brain derived neurotrophic factor gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:7746324 10235 Bdnf brain derived neurotrophic factor gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15115821 10235 Bdnf brain derived neurotrophic factor gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12890780 10235 Bdnf brain derived neurotrophic factor gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15115821 10235 Bdnf brain derived neurotrophic factor gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:17023662 10235 Bdnf brain derived neurotrophic factor gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:16446138 10235 Bdnf brain derived neurotrophic factor gene MP:0000836 abnormal substantia nigra morphology IAGP N RGD:5509061 20141003 MGI PMID:15987955 10235 Bdnf brain derived neurotrophic factor gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0000907 small mesencephalic trigeminal nucleus IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0000907 small mesencephalic trigeminal nucleus IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0000959 abnormal somatic sensory system morphology IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0000960 abnormal sensory ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10681461 10235 Bdnf brain derived neurotrophic factor gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:10681461 10235 Bdnf brain derived neurotrophic factor gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:7568031 10235 Bdnf brain derived neurotrophic factor gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:10681461 10235 Bdnf brain derived neurotrophic factor gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:10725924 10235 Bdnf brain derived neurotrophic factor gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:7568031 10235 Bdnf brain derived neurotrophic factor gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:7746324 10235 Bdnf brain derived neurotrophic factor gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:7746325 10235 Bdnf brain derived neurotrophic factor gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:9364058 10235 Bdnf brain derived neurotrophic factor gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15126035 10235 Bdnf brain derived neurotrophic factor gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:16009525 10235 Bdnf brain derived neurotrophic factor gene MP:0001007 abnormal sympathetic system morphology IAGP N RGD:5509061 20141003 MGI PMID:9786221 10235 Bdnf brain derived neurotrophic factor gene MP:0001021 small L4 dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0001021 small L4 dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0001021 small L4 dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:9364058 10235 Bdnf brain derived neurotrophic factor gene MP:0001026 abnormal adrenergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9786221 10235 Bdnf brain derived neurotrophic factor gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10995552 10235 Bdnf brain derived neurotrophic factor gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746325 10235 Bdnf brain derived neurotrophic factor gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:9364058 10235 Bdnf brain derived neurotrophic factor gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746324 10235 Bdnf brain derived neurotrophic factor gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746325 10235 Bdnf brain derived neurotrophic factor gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:9364058 10235 Bdnf brain derived neurotrophic factor gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746324 10235 Bdnf brain derived neurotrophic factor gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746325 10235 Bdnf brain derived neurotrophic factor gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:9364058 10235 Bdnf brain derived neurotrophic factor gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:10681461 10235 Bdnf brain derived neurotrophic factor gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746324 10235 Bdnf brain derived neurotrophic factor gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746325 10235 Bdnf brain derived neurotrophic factor gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:9364058 10235 Bdnf brain derived neurotrophic factor gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:11579207 10235 Bdnf brain derived neurotrophic factor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17023662 10235 Bdnf brain derived neurotrophic factor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19158294 10235 Bdnf brain derived neurotrophic factor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20130183 10235 Bdnf brain derived neurotrophic factor gene MP:0001260 increased body weight IAGP N RGD:5509061 20231123 MGI PMID:32492978 10235 Bdnf brain derived neurotrophic factor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:11579207 10235 Bdnf brain derived neurotrophic factor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12890780 10235 Bdnf brain derived neurotrophic factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10725924 10235 Bdnf brain derived neurotrophic factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12890780 10235 Bdnf brain derived neurotrophic factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20130183 10235 Bdnf brain derived neurotrophic factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7568031 10235 Bdnf brain derived neurotrophic factor gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16478623 10235 Bdnf brain derived neurotrophic factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10363708 10235 Bdnf brain derived neurotrophic factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:12890780 10235 Bdnf brain derived neurotrophic factor gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20130183 10235 Bdnf brain derived neurotrophic factor gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:10611369 10235 Bdnf brain derived neurotrophic factor gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:11579207 10235 Bdnf brain derived neurotrophic factor gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:17023662 10235 Bdnf brain derived neurotrophic factor gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:19158294 10235 Bdnf brain derived neurotrophic factor gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:11579207 10235 Bdnf brain derived neurotrophic factor gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17023662 10235 Bdnf brain derived neurotrophic factor gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20130183 10235 Bdnf brain derived neurotrophic factor gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10725924 10235 Bdnf brain derived neurotrophic factor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11579207 10235 Bdnf brain derived neurotrophic factor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15249684 10235 Bdnf brain derived neurotrophic factor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:7746324 10235 Bdnf brain derived neurotrophic factor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16478623 10235 Bdnf brain derived neurotrophic factor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15987955 10235 Bdnf brain derived neurotrophic factor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:7746325 10235 Bdnf brain derived neurotrophic factor gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:10725924 10235 Bdnf brain derived neurotrophic factor gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0001411 spinning IAGP N RGD:5509061 20141003 MGI PMID:10725924 10235 Bdnf brain derived neurotrophic factor gene MP:0001411 spinning IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0001411 spinning IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:10725924 10235 Bdnf brain derived neurotrophic factor gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17023662 10235 Bdnf brain derived neurotrophic factor gene MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20141003 MGI PMID:16697351 10235 Bdnf brain derived neurotrophic factor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:10611369 10235 Bdnf brain derived neurotrophic factor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:11579207 10235 Bdnf brain derived neurotrophic factor gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:12890780 10235 Bdnf brain derived neurotrophic factor gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20231123 MGI PMID:32492978 10235 Bdnf brain derived neurotrophic factor gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15249684 10235 Bdnf brain derived neurotrophic factor gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15249684 10235 Bdnf brain derived neurotrophic factor gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17023662 10235 Bdnf brain derived neurotrophic factor gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12971897 10235 Bdnf brain derived neurotrophic factor gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:15249684 10235 Bdnf brain derived neurotrophic factor gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18204444 10235 Bdnf brain derived neurotrophic factor gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:7568031 10235 Bdnf brain derived neurotrophic factor gene MP:0001499 abnormal kindling response IAGP N RGD:5509061 20141003 MGI PMID:15233915 10235 Bdnf brain derived neurotrophic factor gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15115821 10235 Bdnf brain derived neurotrophic factor gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15987955 10235 Bdnf brain derived neurotrophic factor gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16446138 10235 Bdnf brain derived neurotrophic factor gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20130183 10235 Bdnf brain derived neurotrophic factor gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:7746324 10235 Bdnf brain derived neurotrophic factor gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:7746324 10235 Bdnf brain derived neurotrophic factor gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:7568031 10235 Bdnf brain derived neurotrophic factor gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:7568031 10235 Bdnf brain derived neurotrophic factor gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:7746325 10235 Bdnf brain derived neurotrophic factor gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20130183 10235 Bdnf brain derived neurotrophic factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7568031 10235 Bdnf brain derived neurotrophic factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7746324 10235 Bdnf brain derived neurotrophic factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7746325 10235 Bdnf brain derived neurotrophic factor gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11579207 10235 Bdnf brain derived neurotrophic factor gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:7568031 10235 Bdnf brain derived neurotrophic factor gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:12890780 10235 Bdnf brain derived neurotrophic factor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10725924 10235 Bdnf brain derived neurotrophic factor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11579207 10235 Bdnf brain derived neurotrophic factor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10725924 10235 Bdnf brain derived neurotrophic factor gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10611369 10235 Bdnf brain derived neurotrophic factor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11579207 10235 Bdnf brain derived neurotrophic factor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12890780 10235 Bdnf brain derived neurotrophic factor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16446138 10235 Bdnf brain derived neurotrophic factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10725924 10235 Bdnf brain derived neurotrophic factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11579207 10235 Bdnf brain derived neurotrophic factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12971897 10235 Bdnf brain derived neurotrophic factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19136973 10235 Bdnf brain derived neurotrophic factor gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:16446138 10235 Bdnf brain derived neurotrophic factor gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:20130183 10235 Bdnf brain derived neurotrophic factor gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:9786221 10235 Bdnf brain derived neurotrophic factor gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:10611369 10235 Bdnf brain derived neurotrophic factor gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22492034 10235 Bdnf brain derived neurotrophic factor gene MP:0002573 behavioral despair IAGP N RGD:5509061 20231123 MGI PMID:32492978 10235 Bdnf brain derived neurotrophic factor gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10334567 10235 Bdnf brain derived neurotrophic factor gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:9364058 10235 Bdnf brain derived neurotrophic factor gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:10611369 10235 Bdnf brain derived neurotrophic factor gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9364058 10235 Bdnf brain derived neurotrophic factor gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16478623 10235 Bdnf brain derived neurotrophic factor gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20130183 10235 Bdnf brain derived neurotrophic factor gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9472042 10235 Bdnf brain derived neurotrophic factor gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:7568031 10235 Bdnf brain derived neurotrophic factor gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19293383 10235 Bdnf brain derived neurotrophic factor gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9472042 10235 Bdnf brain derived neurotrophic factor gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10681461 10235 Bdnf brain derived neurotrophic factor gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10995552 10235 Bdnf brain derived neurotrophic factor gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:10611369 10235 Bdnf brain derived neurotrophic factor gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22492034 10235 Bdnf brain derived neurotrophic factor gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:10611369 10235 Bdnf brain derived neurotrophic factor gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:20130183 10235 Bdnf brain derived neurotrophic factor gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:16697351 10235 Bdnf brain derived neurotrophic factor gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:19293383 10235 Bdnf brain derived neurotrophic factor gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:22492034 10235 Bdnf brain derived neurotrophic factor gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9364058 10235 Bdnf brain derived neurotrophic factor gene MP:0003877 abnormal serotonergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10611369 10235 Bdnf brain derived neurotrophic factor gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11579207 10235 Bdnf brain derived neurotrophic factor gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746324 10235 Bdnf brain derived neurotrophic factor gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746325 10235 Bdnf brain derived neurotrophic factor gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:8674435 10235 Bdnf brain derived neurotrophic factor gene MP:0003989 abnormal barrel cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16009525 10235 Bdnf brain derived neurotrophic factor gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:16478623 10235 Bdnf brain derived neurotrophic factor gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19293383 10235 Bdnf brain derived neurotrophic factor gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0004298 vestibular ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0004298 vestibular ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:8674435 10235 Bdnf brain derived neurotrophic factor gene MP:0004428 abnormal type I vestibular cell IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0004747 abnormal cochlear OHC afferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12925599 10235 Bdnf brain derived neurotrophic factor gene MP:0004747 abnormal cochlear OHC afferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:8674435 10235 Bdnf brain derived neurotrophic factor gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:17023662 10235 Bdnf brain derived neurotrophic factor gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:19293383 10235 Bdnf brain derived neurotrophic factor gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:16446138 10235 Bdnf brain derived neurotrophic factor gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17493809 10235 Bdnf brain derived neurotrophic factor gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:10611369 10235 Bdnf brain derived neurotrophic factor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11579207 10235 Bdnf brain derived neurotrophic factor gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:16446138 10235 Bdnf brain derived neurotrophic factor gene MP:0005500 abnormal gustatory system morphology IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11579207 10235 Bdnf brain derived neurotrophic factor gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0005655 increased aggression IAGP N RGD:5509061 20141003 MGI PMID:12890780 10235 Bdnf brain derived neurotrophic factor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11579207 10235 Bdnf brain derived neurotrophic factor gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:12890780 10235 Bdnf brain derived neurotrophic factor gene MP:0006257 abnormal fungiform papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:10363708 10235 Bdnf brain derived neurotrophic factor gene MP:0006257 abnormal fungiform papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0006258 abnormal circumvallate papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:10363708 10235 Bdnf brain derived neurotrophic factor gene MP:0006260 abnormal gustatory papilla taste bud morphology IAGP N RGD:5509061 20141003 MGI PMID:10363708 10235 Bdnf brain derived neurotrophic factor gene MP:0006260 abnormal gustatory papilla taste bud morphology IAGP N RGD:5509061 20141003 MGI PMID:15126035 10235 Bdnf brain derived neurotrophic factor gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:17023662 10235 Bdnf brain derived neurotrophic factor gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:20130183 10235 Bdnf brain derived neurotrophic factor gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22492034 10235 Bdnf brain derived neurotrophic factor gene MP:0008265 abnormal hippocampus CA2 region morphology IAGP N RGD:5509061 20141003 MGI PMID:16446138 10235 Bdnf brain derived neurotrophic factor gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15115821 10235 Bdnf brain derived neurotrophic factor gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:9472042 10235 Bdnf brain derived neurotrophic factor gene MP:0008960 abnormal axon pruning IAGP N RGD:5509061 20141003 MGI PMID:18382462 10235 Bdnf brain derived neurotrophic factor gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:20133801 10235 Bdnf brain derived neurotrophic factor gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15249684 10235 Bdnf brain derived neurotrophic factor gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:22492034 10235 Bdnf brain derived neurotrophic factor gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:10681461 10235 Bdnf brain derived neurotrophic factor gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20130183 10235 Bdnf brain derived neurotrophic factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7568031 10235 Bdnf brain derived neurotrophic factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7746324 10235 Bdnf brain derived neurotrophic factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7746325 10235 Bdnf brain derived neurotrophic factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8137432 10235 Bdnf brain derived neurotrophic factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9364058 10235 Bdnf brain derived neurotrophic factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7746324 10235 Bdnf brain derived neurotrophic factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9364058 10235 Bdnf brain derived neurotrophic factor gene MP:0011939 increased food intake IAGP N RGD:5509061 20231123 MGI PMID:32492978 10235 Bdnf brain derived neurotrophic factor gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:15115821 10235 Bdnf brain derived neurotrophic factor gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:20130183 10235 Bdnf brain derived neurotrophic factor gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20141003 MGI PMID:15987955 10235 Bdnf brain derived neurotrophic factor gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20160304 MGI PMID:10514401 10235 Bdnf brain derived neurotrophic factor gene MP:0014490 abnormal inner ear vestibular sensory neuron innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:12620975 10235 Bdnf brain derived neurotrophic factor gene MP:0014490 abnormal inner ear vestibular sensory neuron innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:8139657 10235 Bdnf brain derived neurotrophic factor gene MP:0014490 abnormal inner ear vestibular sensory neuron innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:8674435 10235 Bdnf brain derived neurotrophic factor gene MP:0014491 abnormal mammary gland sensory innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:23224557 10235 Bdnf brain derived neurotrophic factor gene MP:0020083 decreased hippocampus volume IAGP N RGD:5509061 20170706 MGI PMID:17023662 10235 Bdnf brain derived neurotrophic factor gene MP:0020301 short tongue IAGP N RGD:5509061 20221027 MGI PMID:10363708 10235 Bdnf brain derived neurotrophic factor gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:16697351 10236 Cfb complement factor B gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20210128 MGI 10236 Cfb complement factor B gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 10236 Cfb complement factor B gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:9238044 10236 Cfb complement factor B gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 10236 Cfb complement factor B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12091909 10236 Cfb complement factor B gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12794146 10236 Cfb complement factor B gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:9238044 10236 Cfb complement factor B gene MP:0002472 impaired complement alternative pathway IAGP N RGD:5509061 20141003 MGI PMID:9238044 10236 Cfb complement factor B gene MP:0002473 impaired complement classical pathway IAGP N RGD:5509061 20141003 MGI PMID:17916747 10236 Cfb complement factor B gene MP:0002608 increased hematocrit IEA N RGD:5509061 20201022 MGI 10236 Cfb complement factor B gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20160421 MGI 10236 Cfb complement factor B gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:15048732 10236 Cfb complement factor B gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160421 MGI 10236 Cfb complement factor B gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20221215 MGI 10236 Cfb complement factor B gene MP:0020216 decreased circulating complement protein level IAGP N RGD:5509061 20201002 MGI PMID:12091909 10236 Cfb complement factor B gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:12091909 10236 Cfb complement factor B gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200625 MGI PMID:30301856 10237 Bfsp1 beaded filament structural protein 1, in lens-CP94 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 10237 Bfsp1 beaded filament structural protein 1, in lens-CP94 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:14638724 10237 Bfsp1 beaded filament structural protein 1, in lens-CP94 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20181227 MGI 10237 Bfsp1 beaded filament structural protein 1, in lens-CP94 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 10237 Bfsp1 beaded filament structural protein 1, in lens-CP94 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:14638724 10237 Bfsp1 beaded filament structural protein 1, in lens-CP94 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20181227 MGI 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21333348 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:21333348 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19103808 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:8684484 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21333348 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:21333348 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:8684484 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:8684484 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:8684484 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0004149 increased bone strength IAGP N RGD:5509061 20141003 MGI PMID:8684484 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:8684484 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21333348 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:21333348 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:21333348 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:8684484 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:21333348 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:21333348 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:8684484 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21333348 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:21333348 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:8684484 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21333348 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20170803 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:17693256 10238 Bglap2 bone gamma-carboxyglutamate protein 2 gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:17693256 10239 Bgn biglycan gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12102052 10239 Bgn biglycan gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:9731537 10239 Bgn biglycan gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9731537 10239 Bgn biglycan gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9731537 10239 Bgn biglycan gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9731537 10239 Bgn biglycan gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:9731537 10239 Bgn biglycan gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20151217 MGI PMID:16612079 10239 Bgn biglycan gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:9731537 10239 Bgn biglycan gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:12102052 10239 Bgn biglycan gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 10239 Bgn biglycan gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21502335 10239 Bgn biglycan gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9731537 10239 Bgn biglycan gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160505 MGI PMID:19932218 10239 Bgn biglycan gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11978731 10239 Bgn biglycan gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11978731 10239 Bgn biglycan gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:21502335 10239 Bgn biglycan gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21502335 10239 Bgn biglycan gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21502335 10239 Bgn biglycan gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:21502335 10239 Bgn biglycan gene MP:0002294 short gestation period IAGP N RGD:5509061 20141003 MGI PMID:21502335 10239 Bgn biglycan gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:11978731 10239 Bgn biglycan gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:12102052 10239 Bgn biglycan gene MP:0003098 decreased tendon stiffness IAGP N RGD:5509061 20141003 MGI PMID:11978731 10239 Bgn biglycan gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:9731537 10239 Bgn biglycan gene MP:0003109 short femur IAGP N RGD:5509061 20160505 MGI PMID:19932218 10239 Bgn biglycan gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:11978731 10239 Bgn biglycan gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20160505 MGI PMID:19932218 10239 Bgn biglycan gene MP:0004126 thin hypodermis IAGP N RGD:5509061 20141003 MGI PMID:12102052 10239 Bgn biglycan gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9731537 10239 Bgn biglycan gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:12102052 10239 Bgn biglycan gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:9731537 10239 Bgn biglycan gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:11978731 10239 Bgn biglycan gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20151217 MGI PMID:16612079 10239 Bgn biglycan gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20151217 MGI PMID:16006154 10239 Bgn biglycan gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:12102052 10239 Bgn biglycan gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11978731 10239 Bgn biglycan gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:12102052 10239 Bgn biglycan gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:9731537 10239 Bgn biglycan gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:12102052 10239 Bgn biglycan gene MP:0010962 decreased compact bone mass IAGP N RGD:5509061 20141003 MGI PMID:12102052 10239 Bgn biglycan gene MP:0011642 abnormal bone collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:12102052 10239 Bgn biglycan gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:11978731 10239 Bgn biglycan gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:12102052 10239 Bgn biglycan gene MP:0012008 delayed parturition IAGP N RGD:5509061 20141003 MGI PMID:21502335 10239 Bgn biglycan gene MP:0012009 early parturition IAGP N RGD:5509061 20141003 MGI PMID:21502335 10239 Bgn biglycan gene MP:0013304 osteophytes IAGP N RGD:5509061 20151217 MGI PMID:16006154 10239 Bgn biglycan gene MP:0013304 osteophytes IAGP N RGD:5509061 20160505 MGI PMID:19932218 10239 Bgn biglycan gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171109 MGI PMID:16006154 10239 Bgn biglycan gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20160505 MGI PMID:19932218 10239 Bgn biglycan gene MP:0030332 accelerated temporomandibular joint osteoarthritis IAGP N RGD:5509061 20171109 MGI PMID:16006154 10239 Bgn biglycan gene MP:0030332 accelerated temporomandibular joint osteoarthritis IAGP N RGD:5509061 20171109 MGI PMID:16612079 10240 Ceacam1 CEA cell adhesion molecule 1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:16619040 10240 Ceacam1 CEA cell adhesion molecule 1 gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20200310 MGI PMID:1648219 10240 Ceacam1 CEA cell adhesion molecule 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17081782 10240 Ceacam1 CEA cell adhesion molecule 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16619040 10240 Ceacam1 CEA cell adhesion molecule 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:22962327 10240 Ceacam1 CEA cell adhesion molecule 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17081782 10240 Ceacam1 CEA cell adhesion molecule 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17081782 10240 Ceacam1 CEA cell adhesion molecule 1 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17081782 10240 Ceacam1 CEA cell adhesion molecule 1 gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:15331748 10240 Ceacam1 CEA cell adhesion molecule 1 gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:20410265 10240 Ceacam1 CEA cell adhesion molecule 1 gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:8380065 10240 Ceacam1 CEA cell adhesion molecule 1 gene MP:0031047 decreased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:11483763 10240 Ceacam1 CEA cell adhesion molecule 1 gene MP:0031047 decreased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:20410265 10243 Sirpa signal-regulatory protein alpha gene MP:0000691 enlarged spleen IEA N RGD:5509061 20190502 MGI 10243 Sirpa signal-regulatory protein alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12167615 10243 Sirpa signal-regulatory protein alpha gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:24036914 10243 Sirpa signal-regulatory protein alpha gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12167615 10243 Sirpa signal-regulatory protein alpha gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:20685990 10243 Sirpa signal-regulatory protein alpha gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12167615 10243 Sirpa signal-regulatory protein alpha gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:24036914 10243 Sirpa signal-regulatory protein alpha gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:24036914 10243 Sirpa signal-regulatory protein alpha gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12167615 10243 Sirpa signal-regulatory protein alpha gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210128 MGI 10243 Sirpa signal-regulatory protein alpha gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:24036914 10243 Sirpa signal-regulatory protein alpha gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:24036914 10243 Sirpa signal-regulatory protein alpha gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 10243 Sirpa signal-regulatory protein alpha gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12167615 10243 Sirpa signal-regulatory protein alpha gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 10243 Sirpa signal-regulatory protein alpha gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15034021 10243 Sirpa signal-regulatory protein alpha gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 10243 Sirpa signal-regulatory protein alpha gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12167615 10243 Sirpa signal-regulatory protein alpha gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 10243 Sirpa signal-regulatory protein alpha gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:24036914 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:18404215 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:18404215 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:20233579 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:17275231 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:10964473 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:10964473 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9664686 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000155 asymmetric rib joints IAGP N RGD:5509061 20141003 MGI PMID:9664686 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9664686 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000168 abnormal bone marrow development IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16100039 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20190502 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15070745 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:12361961 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16100039 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:12975322 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:12975322 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:23226340 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20141003 MGI PMID:12717732 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:11485993 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15070745 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20150716 MGI PMID:23028455 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:9268572 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:10964473 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9268572 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9664686 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:9268572 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000597 delayed hepatic development IAGP N RGD:5509061 20141003 MGI PMID:11485993 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17275231 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:9268572 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001163 abnormal prostate gland anterior lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:9268572 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:16414041 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21471216 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:12717732 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001288 abnormal lens induction IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001288 abnormal lens induction IAGP N RGD:5509061 20141003 MGI PMID:9851982 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:9268572 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17035289 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:9268572 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11857779 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:17275231 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:20233579 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20210520 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:12361961 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:7657163 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20190502 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:7657163 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:17881493 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20141003 MGI PMID:7657163 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:21145505 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17275231 10244 Bmp4 bone morphogenetic protein 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17275231 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17522159 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12975322 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11857779 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11857779 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:12975322 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9664686 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:16414041 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:17275231 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16712836 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20150716 MGI PMID:23028455 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16100039 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:15070745 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:9268572 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:18404215 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15070745 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15070745 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002697 abnormal eye size IAGP N RGD:5509061 20141003 MGI PMID:9268572 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002700 increased opacity of vitreous body IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:23226340 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7657163 10244 Bmp4 bone morphogenetic protein 4 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:10049358 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003099 retina detachment IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003126 abnormal external female genitalia morphology IAGP N RGD:5509061 20150716 MGI PMID:23028455 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:20233579 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:20233579 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003169 abnormal scala media morphology IAGP N RGD:5509061 20141003 MGI PMID:18404215 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20190502 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003445 sirenomelia IAGP N RGD:5509061 20150716 MGI PMID:23028455 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20150716 MGI PMID:23028455 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003584 bifid ureter IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003586 dilated ureter IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:9268572 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:12631064 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:9268572 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20190502 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20211021 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20211021 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003854 abnormal forelimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003856 abnormal hindlimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20190502 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21145505 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20141003 MGI PMID:20233579 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10049358 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20336610 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7657163 10244 Bmp4 bone morphogenetic protein 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9851982 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16100039 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004017 duplex kidney IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:12361961 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004223 hypoplastic trabecular meshwork IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004224 absent trabecular meshwork IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004226 absent Schlemm's canal IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004282 retrognathia IAGP N RGD:5509061 20171214 MGI PMID:12717732 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004380 short frontal bone IAGP N RGD:5509061 20141003 MGI PMID:9268572 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004458 absent alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004459 small alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004468 small zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:9268572 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004517 decreased vestibular hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:17275231 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004539 absent maxilla IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004559 small allantois IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004574 broad limb buds IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004595 abnormal mandibular condyloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16712836 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:9664686 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004670 small vertebral body IAGP N RGD:5509061 20141003 MGI PMID:17035289 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:9664686 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004899 absent temporal bone squamous part IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004911 absent mandibular condyloid process IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004913 absent mandibular angle IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:9268572 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20141003 MGI PMID:11857779 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005195 abnormal posterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005204 abnormal canal of Schlemm morphology IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:7657163 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:16712836 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005226 abnormal vertebral arch development IAGP N RGD:5509061 20141003 MGI PMID:17035289 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005227 abnormal vertebral body development IAGP N RGD:5509061 20141003 MGI PMID:17035289 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:15070745 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:21471216 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21471216 10244 Bmp4 bone morphogenetic protein 4 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16100039 10244 Bmp4 bone morphogenetic protein 4 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20151001 MGI PMID:18404215 10244 Bmp4 bone morphogenetic protein 4 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:18404215 10244 Bmp4 bone morphogenetic protein 4 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18404215 10244 Bmp4 bone morphogenetic protein 4 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20190502 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:21145505 10244 Bmp4 bone morphogenetic protein 4 gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0006241 abnormal placement of pupils IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0006250 abnormal line of Schwalbe morphology IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20150716 MGI PMID:23028455 10244 Bmp4 bone morphogenetic protein 4 gene MP:0006323 abnormal extraembryonic mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:7657163 10244 Bmp4 bone morphogenetic protein 4 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:17275231 10244 Bmp4 bone morphogenetic protein 4 gene MP:0006377 abnormal vestibulocollic reflex IAGP N RGD:5509061 20141003 MGI PMID:17275231 10244 Bmp4 bone morphogenetic protein 4 gene MP:0008259 abnormal optic disk morphology IAGP N RGD:5509061 20190411 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:10964473 10244 Bmp4 bone morphogenetic protein 4 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10049358 10244 Bmp4 bone morphogenetic protein 4 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10894154 10244 Bmp4 bone morphogenetic protein 4 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:18622394 10244 Bmp4 bone morphogenetic protein 4 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:23469192 10244 Bmp4 bone morphogenetic protein 4 gene MP:0008393 absent primordial germ cells IAGP N RGD:5509061 20141003 MGI PMID:10049358 10244 Bmp4 bone morphogenetic protein 4 gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20141003 MGI PMID:18404215 10244 Bmp4 bone morphogenetic protein 4 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0009052 anal stenosis IAGP N RGD:5509061 20150716 MGI PMID:23028455 10244 Bmp4 bone morphogenetic protein 4 gene MP:0009203 external male genitalia hypoplasia IAGP N RGD:5509061 20150716 MGI PMID:23028455 10244 Bmp4 bone morphogenetic protein 4 gene MP:0009252 absent urinary bladder IAGP N RGD:5509061 20150716 MGI PMID:23028455 10244 Bmp4 bone morphogenetic protein 4 gene MP:0009274 buphthalmos IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0009576 oral atresia IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0009874 abnormal interdigital cell death IAGP N RGD:5509061 20141003 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0009905 absent tongue IAGP N RGD:5509061 20141003 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12361961 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010224 abnormal heart ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:21145505 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010252 anterior subcapsular cataract IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010256 anterior cortical cataract IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:12975322 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:12975322 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12975322 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010414 partial atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12975322 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15070745 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010426 abnormal heart and great artery attachment IAGP N RGD:5509061 20141003 MGI PMID:21145505 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:21145505 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010455 aortopulmonary window IAGP N RGD:5509061 20141003 MGI PMID:15070745 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010464 abnormal aortic arch and aortic arch branch attachment IAGP N RGD:5509061 20141003 MGI PMID:15070745 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:15070745 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010587 conotruncal ridge hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15070745 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:12975322 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010656 thick myocardium IAGP N RGD:5509061 20141003 MGI PMID:21145505 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010755 abnormal heart right ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:16100039 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010980 ectopic ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010982 abnormal ureteric bud elongation IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:12631064 10244 Bmp4 bone morphogenetic protein 4 gene MP:0010985 abnormal kidney mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12975322 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11857779 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12975322 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9268572 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10049358 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20336610 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7657163 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7657163 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11485993 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12717732 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21145505 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7657163 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9851982 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12717732 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12717732 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15070745 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:12361961 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011264 abnormal cardiac mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011305 dilated kidney calyx IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:12631064 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12631064 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011426 abnormal ureter smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12631064 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141003 MGI PMID:11722794 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011486 ectopic ureter IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011488 abnormal ureterovesical junction morphology IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:15070745 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011759 absent Rathke's pouch IAGP N RGD:5509061 20141003 MGI PMID:9806931 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011783 abnormal ureteral orifice morphology IAGP N RGD:5509061 20141003 MGI PMID:10749566 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011851 abnormal embryonic cloaca development IAGP N RGD:5509061 20150716 MGI PMID:23028455 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17275231 10244 Bmp4 bone morphogenetic protein 4 gene MP:0012235 abnormal liver bud morphology IAGP N RGD:5509061 20141003 MGI PMID:11485993 10244 Bmp4 bone morphogenetic protein 4 gene MP:0012740 abnormal posterior primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:12361961 10244 Bmp4 bone morphogenetic protein 4 gene MP:0013167 abnormal hindlimb bud morphology IAGP N RGD:5509061 20150716 MGI PMID:23028455 10244 Bmp4 bone morphogenetic protein 4 gene MP:0013283 failure of ventral body wall closure IAGP N RGD:5509061 20141003 MGI PMID:16624858 10244 Bmp4 bone morphogenetic protein 4 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 10244 Bmp4 bone morphogenetic protein 4 gene MP:0013790 single external naris IAGP N RGD:5509061 20150611 MGI PMID:14681194 10244 Bmp4 bone morphogenetic protein 4 gene MP:0014291 decreased autopod size IAGP N RGD:5509061 20230824 MGI PMID:17194222 10244 Bmp4 bone morphogenetic protein 4 gene MP:0020516 abnormal visceral yolk sac mesenchyme morphology IAGP N RGD:5509061 20180125 MGI PMID:7657163 10244 Bmp4 bone morphogenetic protein 4 gene MP:0030066 short face IAGP N RGD:5509061 20171207 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20171005 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0030245 round head IAGP N RGD:5509061 20171019 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0030283 small mandibular coronoid process IAGP N RGD:5509061 20171102 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20171214 MGI PMID:12717732 10244 Bmp4 bone morphogenetic protein 4 gene MP:0030372 enlarged Meckel's cartilage IAGP N RGD:5509061 20171207 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:22219353 10244 Bmp4 bone morphogenetic protein 4 gene MP:0031583 semilunar valve hypoplasia IAGP N RGD:5509061 20240125 MGI PMID:15070745 10245 Bmyc brain expressed myelocytomatosis oncogene gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:22869780 10245 Bmyc brain expressed myelocytomatosis oncogene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22869780 10245 Bmyc brain expressed myelocytomatosis oncogene gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:22869780 10245 Bmyc brain expressed myelocytomatosis oncogene gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22869780 10245 Bmyc brain expressed myelocytomatosis oncogene gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:22869780 10245 Bmyc brain expressed myelocytomatosis oncogene gene MP:0009248 small caput epididymis IAGP N RGD:5509061 20141003 MGI PMID:22869780 10245 Bmyc brain expressed myelocytomatosis oncogene gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22869780 10245 Bmyc brain expressed myelocytomatosis oncogene gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20141003 MGI PMID:22869780 10245 Bmyc brain expressed myelocytomatosis oncogene gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:22869780 10246 Brca1 breast cancer 1, early onset gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:11420664 10246 Brca1 breast cancer 1, early onset gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:10881179 10246 Brca1 breast cancer 1, early onset gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:11431698 10246 Brca1 breast cancer 1, early onset gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:17070800 10246 Brca1 breast cancer 1, early onset gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17070800 10246 Brca1 breast cancer 1, early onset gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17070800 10246 Brca1 breast cancer 1, early onset gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17318223 10246 Brca1 breast cancer 1, early onset gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8698242 10246 Brca1 breast cancer 1, early onset gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20141003 MGI PMID:15485917 10246 Brca1 breast cancer 1, early onset gene MP:0000423 delayed hair regrowth IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17363841 10246 Brca1 breast cancer 1, early onset gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17363841 10246 Brca1 breast cancer 1, early onset gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:11358863 10246 Brca1 breast cancer 1, early onset gene MP:0000621 increased salivary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17212342 10246 Brca1 breast cancer 1, early onset gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:16943438 10246 Brca1 breast cancer 1, early onset gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:22777348 10246 Brca1 breast cancer 1, early onset gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:10319859 10246 Brca1 breast cancer 1, early onset gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:17212342 10246 Brca1 breast cancer 1, early onset gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16943438 10246 Brca1 breast cancer 1, early onset gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:10319859 10246 Brca1 breast cancer 1, early onset gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:15485917 10246 Brca1 breast cancer 1, early onset gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:12555066 10246 Brca1 breast cancer 1, early onset gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10881179 10246 Brca1 breast cancer 1, early onset gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:8563759 10246 Brca1 breast cancer 1, early onset gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11431698 10246 Brca1 breast cancer 1, early onset gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15123655 10246 Brca1 breast cancer 1, early onset gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17318223 10246 Brca1 breast cancer 1, early onset gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:8563759 10246 Brca1 breast cancer 1, early onset gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10942534 10246 Brca1 breast cancer 1, early onset gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:8563759 10246 Brca1 breast cancer 1, early onset gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:15485917 10246 Brca1 breast cancer 1, early onset gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:17070800 10246 Brca1 breast cancer 1, early onset gene MP:0001138 abnormal uterine cervix squamous epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16943438 10246 Brca1 breast cancer 1, early onset gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12642502 10246 Brca1 breast cancer 1, early onset gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:22034435 10246 Brca1 breast cancer 1, early onset gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11358863 10246 Brca1 breast cancer 1, early onset gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22034435 10246 Brca1 breast cancer 1, early onset gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12642502 10246 Brca1 breast cancer 1, early onset gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12934101 10246 Brca1 breast cancer 1, early onset gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15485917 10246 Brca1 breast cancer 1, early onset gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22034435 10246 Brca1 breast cancer 1, early onset gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22777348 10246 Brca1 breast cancer 1, early onset gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22777348 10246 Brca1 breast cancer 1, early onset gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:24120138 10246 Brca1 breast cancer 1, early onset gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20150319 MGI PMID:22617326 10246 Brca1 breast cancer 1, early onset gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:8674108 10246 Brca1 breast cancer 1, early onset gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:8698242 10246 Brca1 breast cancer 1, early onset gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9171368 10246 Brca1 breast cancer 1, early onset gene MP:0001684 abnormal axial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9872327 10246 Brca1 breast cancer 1, early onset gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:11420664 10246 Brca1 breast cancer 1, early onset gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:8674108 10246 Brca1 breast cancer 1, early onset gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20141003 MGI PMID:8698242 10246 Brca1 breast cancer 1, early onset gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11431698 10246 Brca1 breast cancer 1, early onset gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17318223 10246 Brca1 breast cancer 1, early onset gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8563759 10246 Brca1 breast cancer 1, early onset gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8674108 10246 Brca1 breast cancer 1, early onset gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8698242 10246 Brca1 breast cancer 1, early onset gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9207798 10246 Brca1 breast cancer 1, early onset gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9872327 10246 Brca1 breast cancer 1, early onset gene MP:0001710 absent amniotic folds IAGP N RGD:5509061 20141003 MGI PMID:9171368 10246 Brca1 breast cancer 1, early onset gene MP:0001714 absent trophoblast giant cells IAGP N RGD:5509061 20141003 MGI PMID:8674108 10246 Brca1 breast cancer 1, early onset gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:9207798 10246 Brca1 breast cancer 1, early onset gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:9207798 10246 Brca1 breast cancer 1, early onset gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11358863 10246 Brca1 breast cancer 1, early onset gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10319859 10246 Brca1 breast cancer 1, early onset gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15131084 10246 Brca1 breast cancer 1, early onset gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18443292 10246 Brca1 breast cancer 1, early onset gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22777348 10246 Brca1 breast cancer 1, early onset gene MP:0001884 mammary gland alveolar hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17653086 10246 Brca1 breast cancer 1, early onset gene MP:0001885 mammary gland duct hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16943438 10246 Brca1 breast cancer 1, early onset gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11358863 10246 Brca1 breast cancer 1, early onset gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22034435 10246 Brca1 breast cancer 1, early onset gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12555066 10246 Brca1 breast cancer 1, early onset gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:10881179 10246 Brca1 breast cancer 1, early onset gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:12555066 10246 Brca1 breast cancer 1, early onset gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:9872327 10246 Brca1 breast cancer 1, early onset gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:17653086 10246 Brca1 breast cancer 1, early onset gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:12934101 10246 Brca1 breast cancer 1, early onset gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:15797026 10246 Brca1 breast cancer 1, early onset gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11358863 10246 Brca1 breast cancer 1, early onset gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12934101 10246 Brca1 breast cancer 1, early onset gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15131084 10246 Brca1 breast cancer 1, early onset gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15485917 10246 Brca1 breast cancer 1, early onset gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22034435 10246 Brca1 breast cancer 1, early onset gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23712259 10246 Brca1 breast cancer 1, early onset gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12555066 10246 Brca1 breast cancer 1, early onset gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15131084 10246 Brca1 breast cancer 1, early onset gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17363841 10246 Brca1 breast cancer 1, early onset gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20150319 MGI PMID:22617326 10246 Brca1 breast cancer 1, early onset gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12832489 10246 Brca1 breast cancer 1, early onset gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9171368 10246 Brca1 breast cancer 1, early onset gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12555066 10246 Brca1 breast cancer 1, early onset gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15131084 10246 Brca1 breast cancer 1, early onset gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:11420664 10246 Brca1 breast cancer 1, early onset gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12832489 10246 Brca1 breast cancer 1, early onset gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:8674108 10246 Brca1 breast cancer 1, early onset gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:8698242 10246 Brca1 breast cancer 1, early onset gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11420664 10246 Brca1 breast cancer 1, early onset gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12832489 10246 Brca1 breast cancer 1, early onset gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8674108 10246 Brca1 breast cancer 1, early onset gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8698242 10246 Brca1 breast cancer 1, early onset gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9171368 10246 Brca1 breast cancer 1, early onset gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9872327 10246 Brca1 breast cancer 1, early onset gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8674108 10246 Brca1 breast cancer 1, early onset gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11358863 10246 Brca1 breast cancer 1, early onset gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10319859 10246 Brca1 breast cancer 1, early onset gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17212342 10246 Brca1 breast cancer 1, early onset gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18443292 10246 Brca1 breast cancer 1, early onset gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8563759 10246 Brca1 breast cancer 1, early onset gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8674108 10246 Brca1 breast cancer 1, early onset gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8698242 10246 Brca1 breast cancer 1, early onset gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9171368 10246 Brca1 breast cancer 1, early onset gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:9872327 10246 Brca1 breast cancer 1, early onset gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:8674108 10246 Brca1 breast cancer 1, early onset gene MP:0002676 uterus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15485917 10246 Brca1 breast cancer 1, early onset gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:10881179 10246 Brca1 breast cancer 1, early onset gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:8563759 10246 Brca1 breast cancer 1, early onset gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15485917 10246 Brca1 breast cancer 1, early onset gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16943438 10246 Brca1 breast cancer 1, early onset gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:9171368 10246 Brca1 breast cancer 1, early onset gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:18343216 10246 Brca1 breast cancer 1, early onset gene MP:0003401 enlarged tail bud IAGP N RGD:5509061 20141003 MGI PMID:11420664 10246 Brca1 breast cancer 1, early onset gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:22172724 10246 Brca1 breast cancer 1, early onset gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:18343216 10246 Brca1 breast cancer 1, early onset gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20150319 MGI PMID:22617326 10246 Brca1 breast cancer 1, early onset gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20150319 MGI PMID:22617326 10246 Brca1 breast cancer 1, early onset gene MP:0003587 ureter obstruction IAGP N RGD:5509061 20141003 MGI PMID:17653086 10246 Brca1 breast cancer 1, early onset gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:11431698 10246 Brca1 breast cancer 1, early onset gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:15797026 10246 Brca1 breast cancer 1, early onset gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17318223 10246 Brca1 breast cancer 1, early onset gene MP:0003750 increased mouth tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12934101 10246 Brca1 breast cancer 1, early onset gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:8674108 10246 Brca1 breast cancer 1, early onset gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11420664 10246 Brca1 breast cancer 1, early onset gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15123655 10246 Brca1 breast cancer 1, early onset gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22172724 10246 Brca1 breast cancer 1, early onset gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8674108 10246 Brca1 breast cancer 1, early onset gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8698242 10246 Brca1 breast cancer 1, early onset gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9171368 10246 Brca1 breast cancer 1, early onset gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9207798 10246 Brca1 breast cancer 1, early onset gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:8698242 10246 Brca1 breast cancer 1, early onset gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20141003 MGI PMID:9872327 10246 Brca1 breast cancer 1, early onset gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:15123655 10246 Brca1 breast cancer 1, early onset gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:17318223 10246 Brca1 breast cancer 1, early onset gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:23657012 10246 Brca1 breast cancer 1, early onset gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:10881179 10246 Brca1 breast cancer 1, early onset gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:9872327 10246 Brca1 breast cancer 1, early onset gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:10881179 10246 Brca1 breast cancer 1, early onset gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:11431698 10246 Brca1 breast cancer 1, early onset gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9207798 10246 Brca1 breast cancer 1, early onset gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12934101 10246 Brca1 breast cancer 1, early onset gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17363841 10246 Brca1 breast cancer 1, early onset gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:15485917 10246 Brca1 breast cancer 1, early onset gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20210826 MGI PMID:33857404 10246 Brca1 breast cancer 1, early onset gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8674108 10246 Brca1 breast cancer 1, early onset gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:10881179 10246 Brca1 breast cancer 1, early onset gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10881179 10246 Brca1 breast cancer 1, early onset gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10881179 10246 Brca1 breast cancer 1, early onset gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:12642502 10246 Brca1 breast cancer 1, early onset gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:22034435 10246 Brca1 breast cancer 1, early onset gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12642502 10246 Brca1 breast cancer 1, early onset gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11420664 10246 Brca1 breast cancer 1, early onset gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11431698 10246 Brca1 breast cancer 1, early onset gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:10319859 10246 Brca1 breast cancer 1, early onset gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:10319859 10246 Brca1 breast cancer 1, early onset gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:12642502 10246 Brca1 breast cancer 1, early onset gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:10881179 10246 Brca1 breast cancer 1, early onset gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20150319 MGI PMID:22617326 10246 Brca1 breast cancer 1, early onset gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:22034435 10246 Brca1 breast cancer 1, early onset gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:22777348 10246 Brca1 breast cancer 1, early onset gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24120138 10246 Brca1 breast cancer 1, early onset gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10881179 10246 Brca1 breast cancer 1, early onset gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20160310 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12642502 10246 Brca1 breast cancer 1, early onset gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:10881179 10246 Brca1 breast cancer 1, early onset gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:15131084 10246 Brca1 breast cancer 1, early onset gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20210826 MGI PMID:33857404 10246 Brca1 breast cancer 1, early onset gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16943438 10246 Brca1 breast cancer 1, early onset gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16943438 10246 Brca1 breast cancer 1, early onset gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:17653086 10246 Brca1 breast cancer 1, early onset gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16943438 10246 Brca1 breast cancer 1, early onset gene MP:0009505 abnormal mammary gland lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0009508 increased mammary gland ductal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16943438 10246 Brca1 breast cancer 1, early onset gene MP:0009508 increased mammary gland ductal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17212342 10246 Brca1 breast cancer 1, early onset gene MP:0009566 meiotic nondisjunction IAGP N RGD:5509061 20141003 MGI PMID:12642502 10246 Brca1 breast cancer 1, early onset gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12934101 10246 Brca1 breast cancer 1, early onset gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20141003 MGI PMID:9171368 10246 Brca1 breast cancer 1, early onset gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17363841 10246 Brca1 breast cancer 1, early onset gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23509290 10246 Brca1 breast cancer 1, early onset gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22034435 10246 Brca1 breast cancer 1, early onset gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22172724 10246 Brca1 breast cancer 1, early onset gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0010173 increased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17653086 10246 Brca1 breast cancer 1, early onset gene MP:0010173 increased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20160317 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22777348 10246 Brca1 breast cancer 1, early onset gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15485917 10246 Brca1 breast cancer 1, early onset gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22172724 10246 Brca1 breast cancer 1, early onset gene MP:0010285 decreased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22172724 10246 Brca1 breast cancer 1, early onset gene MP:0010287 increased reproductive system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12934101 10246 Brca1 breast cancer 1, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10319859 10246 Brca1 breast cancer 1, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11358863 10246 Brca1 breast cancer 1, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11431698 10246 Brca1 breast cancer 1, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15131084 10246 Brca1 breast cancer 1, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15485917 10246 Brca1 breast cancer 1, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16943438 10246 Brca1 breast cancer 1, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17212342 10246 Brca1 breast cancer 1, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17626182 10246 Brca1 breast cancer 1, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17653086 10246 Brca1 breast cancer 1, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22172724 10246 Brca1 breast cancer 1, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22777348 10246 Brca1 breast cancer 1, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24120138 10246 Brca1 breast cancer 1, early onset gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12934101 10246 Brca1 breast cancer 1, early onset gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22172724 10246 Brca1 breast cancer 1, early onset gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:12934101 10246 Brca1 breast cancer 1, early onset gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22034435 10246 Brca1 breast cancer 1, early onset gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22172724 10246 Brca1 breast cancer 1, early onset gene MP:0010343 increased lipoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15485917 10246 Brca1 breast cancer 1, early onset gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20141003 MGI PMID:22172724 10246 Brca1 breast cancer 1, early onset gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:23509290 10246 Brca1 breast cancer 1, early onset gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20190523 MGI PMID:25066119 10246 Brca1 breast cancer 1, early onset gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12533509 10246 Brca1 breast cancer 1, early onset gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11431698 10246 Brca1 breast cancer 1, early onset gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15123655 10246 Brca1 breast cancer 1, early onset gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17626182 10246 Brca1 breast cancer 1, early onset gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18443292 10246 Brca1 breast cancer 1, early onset gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9171368 10246 Brca1 breast cancer 1, early onset gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9872327 10246 Brca1 breast cancer 1, early onset gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8674108 10246 Brca1 breast cancer 1, early onset gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8698242 10246 Brca1 breast cancer 1, early onset gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10942534 10246 Brca1 breast cancer 1, early onset gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11170347 10246 Brca1 breast cancer 1, early onset gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22172724 10246 Brca1 breast cancer 1, early onset gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8563759 10246 Brca1 breast cancer 1, early onset gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9207798 10246 Brca1 breast cancer 1, early onset gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9872327 10246 Brca1 breast cancer 1, early onset gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17318223 10246 Brca1 breast cancer 1, early onset gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22777348 10246 Brca1 breast cancer 1, early onset gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11358863 10246 Brca1 breast cancer 1, early onset gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12934101 10246 Brca1 breast cancer 1, early onset gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:8674108 10246 Brca1 breast cancer 1, early onset gene MP:0011187 abnormal parietal endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:8674108 10246 Brca1 breast cancer 1, early onset gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:11431698 10246 Brca1 breast cancer 1, early onset gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22034435 10246 Brca1 breast cancer 1, early onset gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15485917 10246 Brca1 breast cancer 1, early onset gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20150319 MGI PMID:22617326 10246 Brca1 breast cancer 1, early onset gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150219 MGI PMID:11431698 10246 Brca1 breast cancer 1, early onset gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:12642502 10246 Brca1 breast cancer 1, early onset gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20160310 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0014126 increased mammary gland apoptosis IAGP N RGD:5509061 20160317 MGI PMID:19996295 10246 Brca1 breast cancer 1, early onset gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:24120138 10246 Brca1 breast cancer 1, early onset gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:17318223 10246 Brca1 breast cancer 1, early onset gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:15123655 10246 Brca1 breast cancer 1, early onset gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:16943438 10246 Brca1 breast cancer 1, early onset gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:22034435 10246 Brca1 breast cancer 1, early onset gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20230824 MGI PMID:17318223 10247 Brca2 breast cancer 2, early onset gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16859999 10247 Brca2 breast cancer 2, early onset gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:11215675 10247 Brca2 breast cancer 2, early onset gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11215675 10247 Brca2 breast cancer 2, early onset gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:20585617 10247 Brca2 breast cancer 2, early onset gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:11861370 10247 Brca2 breast cancer 2, early onset gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20220602 MGI PMID:35365640 10247 Brca2 breast cancer 2, early onset gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16859999 10247 Brca2 breast cancer 2, early onset gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9171368 10247 Brca2 breast cancer 2, early onset gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10942534 10247 Brca2 breast cancer 2, early onset gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11215675 10247 Brca2 breast cancer 2, early onset gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11215675 10247 Brca2 breast cancer 2, early onset gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:11215675 10247 Brca2 breast cancer 2, early onset gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11215675 10247 Brca2 breast cancer 2, early onset gene MP:0001140 abnormal vagina epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11215675 10247 Brca2 breast cancer 2, early onset gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0001147 small testis IAGP N RGD:5509061 20190502 MGI PMID:30305635 10247 Brca2 breast cancer 2, early onset gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:20585617 10247 Brca2 breast cancer 2, early onset gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0001241 absent epidermis stratum corneum IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16859999 10247 Brca2 breast cancer 2, early onset gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220602 MGI PMID:35365640 10247 Brca2 breast cancer 2, early onset gene MP:0001265 decreased body size IAGP N RGD:5509061 20220602 MGI PMID:35365640 10247 Brca2 breast cancer 2, early onset gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16859999 10247 Brca2 breast cancer 2, early onset gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:11694875 10247 Brca2 breast cancer 2, early onset gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:9171368 10247 Brca2 breast cancer 2, early onset gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9171368 10247 Brca2 breast cancer 2, early onset gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20220602 MGI PMID:35365640 10247 Brca2 breast cancer 2, early onset gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:9171368 10247 Brca2 breast cancer 2, early onset gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:12414647 10247 Brca2 breast cancer 2, early onset gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11494122 10247 Brca2 breast cancer 2, early onset gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11694875 10247 Brca2 breast cancer 2, early onset gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9537225 10247 Brca2 breast cancer 2, early onset gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9537225 10247 Brca2 breast cancer 2, early onset gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12414647 10247 Brca2 breast cancer 2, early onset gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21056012 10247 Brca2 breast cancer 2, early onset gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11694875 10247 Brca2 breast cancer 2, early onset gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11861370 10247 Brca2 breast cancer 2, early onset gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12414647 10247 Brca2 breast cancer 2, early onset gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:11215675 10247 Brca2 breast cancer 2, early onset gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9537225 10247 Brca2 breast cancer 2, early onset gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21056012 10247 Brca2 breast cancer 2, early onset gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12619154 10247 Brca2 breast cancer 2, early onset gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14981540 10247 Brca2 breast cancer 2, early onset gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:10942534 10247 Brca2 breast cancer 2, early onset gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9171368 10247 Brca2 breast cancer 2, early onset gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12619154 10247 Brca2 breast cancer 2, early onset gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21056012 10247 Brca2 breast cancer 2, early onset gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9537225 10247 Brca2 breast cancer 2, early onset gene MP:0002083 premature death IAGP N RGD:5509061 20220602 MGI PMID:35365640 10247 Brca2 breast cancer 2, early onset gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:9126738 10247 Brca2 breast cancer 2, early onset gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9126738 10247 Brca2 breast cancer 2, early onset gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9171368 10247 Brca2 breast cancer 2, early onset gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9126738 10247 Brca2 breast cancer 2, early onset gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9171368 10247 Brca2 breast cancer 2, early onset gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9537225 10247 Brca2 breast cancer 2, early onset gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11494122 10247 Brca2 breast cancer 2, early onset gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11694875 10247 Brca2 breast cancer 2, early onset gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12414647 10247 Brca2 breast cancer 2, early onset gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9126738 10247 Brca2 breast cancer 2, early onset gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16859999 10247 Brca2 breast cancer 2, early onset gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0003335 exocrine pancreatic insufficiency IAGP N RGD:5509061 20141003 MGI PMID:21056012 10247 Brca2 breast cancer 2, early onset gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:19164512 10247 Brca2 breast cancer 2, early onset gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:20585617 10247 Brca2 breast cancer 2, early onset gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:12414647 10247 Brca2 breast cancer 2, early onset gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:16859999 10247 Brca2 breast cancer 2, early onset gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12414647 10247 Brca2 breast cancer 2, early onset gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16546942 10247 Brca2 breast cancer 2, early onset gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10942534 10247 Brca2 breast cancer 2, early onset gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11694875 10247 Brca2 breast cancer 2, early onset gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9537225 10247 Brca2 breast cancer 2, early onset gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:16859999 10247 Brca2 breast cancer 2, early onset gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20220602 MGI PMID:35365640 10247 Brca2 breast cancer 2, early onset gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:12414647 10247 Brca2 breast cancer 2, early onset gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:23657012 10247 Brca2 breast cancer 2, early onset gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:15375219 10247 Brca2 breast cancer 2, early onset gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12414647 10247 Brca2 breast cancer 2, early onset gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11215675 10247 Brca2 breast cancer 2, early onset gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:14981540 10247 Brca2 breast cancer 2, early onset gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:9171368 10247 Brca2 breast cancer 2, early onset gene MP:0004806 absent germ cells IAGP N RGD:5509061 20141003 MGI PMID:9537225 10247 Brca2 breast cancer 2, early onset gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:11215675 10247 Brca2 breast cancer 2, early onset gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20190502 MGI PMID:30305635 10247 Brca2 breast cancer 2, early onset gene MP:0004894 uterus atrophy IAGP N RGD:5509061 20141003 MGI PMID:11215675 10247 Brca2 breast cancer 2, early onset gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:9537225 10247 Brca2 breast cancer 2, early onset gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:9171368 10247 Brca2 breast cancer 2, early onset gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:12619154 10247 Brca2 breast cancer 2, early onset gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14981540 10247 Brca2 breast cancer 2, early onset gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14981540 10247 Brca2 breast cancer 2, early onset gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19164512 10247 Brca2 breast cancer 2, early onset gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12414647 10247 Brca2 breast cancer 2, early onset gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20150319 MGI PMID:22617326 10247 Brca2 breast cancer 2, early onset gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:12619154 10247 Brca2 breast cancer 2, early onset gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:16859999 10247 Brca2 breast cancer 2, early onset gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20190502 MGI PMID:30305635 10247 Brca2 breast cancer 2, early onset gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:11861370 10247 Brca2 breast cancer 2, early onset gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:16546942 10247 Brca2 breast cancer 2, early onset gene MP:0008780 increased pancreatic acinar cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21056012 10247 Brca2 breast cancer 2, early onset gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:16859999 10247 Brca2 breast cancer 2, early onset gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:12619154 10247 Brca2 breast cancer 2, early onset gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:16859999 10247 Brca2 breast cancer 2, early onset gene MP:0009078 adrenal gland hyperplasia IAGP N RGD:5509061 20141120 MGI PMID:11215675 10247 Brca2 breast cancer 2, early onset gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21056012 10247 Brca2 breast cancer 2, early onset gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:20585617 10247 Brca2 breast cancer 2, early onset gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20190502 MGI PMID:30305635 10247 Brca2 breast cancer 2, early onset gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20220602 MGI PMID:35365640 10247 Brca2 breast cancer 2, early onset gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20220602 MGI PMID:35365640 10247 Brca2 breast cancer 2, early onset gene MP:0009733 absent nipple IAGP N RGD:5509061 20141003 MGI PMID:11215675 10247 Brca2 breast cancer 2, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11215675 10247 Brca2 breast cancer 2, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11694875 10247 Brca2 breast cancer 2, early onset gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16546942 10247 Brca2 breast cancer 2, early onset gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11694875 10247 Brca2 breast cancer 2, early onset gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16546942 10247 Brca2 breast cancer 2, early onset gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:12619154 10247 Brca2 breast cancer 2, early onset gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9537225 10247 Brca2 breast cancer 2, early onset gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9537225 10247 Brca2 breast cancer 2, early onset gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9537225 10247 Brca2 breast cancer 2, early onset gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9126738 10247 Brca2 breast cancer 2, early onset gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11694875 10247 Brca2 breast cancer 2, early onset gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12619154 10247 Brca2 breast cancer 2, early onset gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9171368 10247 Brca2 breast cancer 2, early onset gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10942534 10247 Brca2 breast cancer 2, early onset gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10942534 10247 Brca2 breast cancer 2, early onset gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14981540 10247 Brca2 breast cancer 2, early onset gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9537225 10247 Brca2 breast cancer 2, early onset gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20220602 MGI PMID:35365640 10247 Brca2 breast cancer 2, early onset gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9537225 10247 Brca2 breast cancer 2, early onset gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11861370 10247 Brca2 breast cancer 2, early onset gene MP:0011197 abnormal proamniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:9171368 10247 Brca2 breast cancer 2, early onset gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12414647 10247 Brca2 breast cancer 2, early onset gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12619154 10247 Brca2 breast cancer 2, early onset gene MP:0013220 increased pancreas apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21056012 10247 Brca2 breast cancer 2, early onset gene MP:0013236 ovary degeneration IAGP N RGD:5509061 20141120 MGI PMID:9398843 10247 Brca2 breast cancer 2, early onset gene MP:0031174 decreased mammary duct terminal end bud number IAGP N RGD:5509061 20220602 MGI PMID:35365640 10248 Bsg basigin gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:9501026 10248 Bsg basigin gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:9501026 10248 Bsg basigin gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141030 MGI PMID:24391450 10248 Bsg basigin gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0001147 small testis IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220224 MGI PMID:9501026 10248 Bsg basigin gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:9501026 10248 Bsg basigin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9501026 10248 Bsg basigin gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141030 MGI PMID:24391450 10248 Bsg basigin gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:9501026 10248 Bsg basigin gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9501026 10248 Bsg basigin gene MP:0001925 male infertility IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9501026 10248 Bsg basigin gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9501026 10248 Bsg basigin gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20200611 MGI PMID:25891969 10248 Bsg basigin gene MP:0002871 albuminuria IAGP N RGD:5509061 20200611 MGI PMID:25891969 10248 Bsg basigin gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20200611 MGI PMID:25891969 10248 Bsg basigin gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20191212 MGI PMID:10967074 10248 Bsg basigin gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20191212 MGI PMID:10967074 10248 Bsg basigin gene MP:0004728 abnormal efferent ductules of testis morphology IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20200611 MGI PMID:25891969 10248 Bsg basigin gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20200611 MGI PMID:25891969 10248 Bsg basigin gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141030 MGI PMID:24391450 10248 Bsg basigin gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141030 MGI PMID:24391450 10248 Bsg basigin gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:9501026 10248 Bsg basigin gene MP:0005159 azoospermia IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200611 MGI PMID:25891969 10248 Bsg basigin gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141030 MGI PMID:24391450 10248 Bsg basigin gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0006428 ectopic Sertoli cells IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141030 MGI PMID:24391450 10248 Bsg basigin gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:9501026 10248 Bsg basigin gene MP:0008447 absent retina cone cells IAGP N RGD:5509061 20191212 MGI PMID:10967074 10248 Bsg basigin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20191212 MGI PMID:10967074 10248 Bsg basigin gene MP:0008454 absent retina rod cells IAGP N RGD:5509061 20191212 MGI PMID:10967074 10248 Bsg basigin gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20191212 MGI PMID:10967074 10248 Bsg basigin gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20191212 MGI PMID:10967074 10248 Bsg basigin gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20191212 MGI PMID:10967074 10248 Bsg basigin gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20200611 MGI PMID:25891969 10248 Bsg basigin gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20200611 MGI PMID:25891969 10248 Bsg basigin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9501026 10248 Bsg basigin gene MP:0011103 embryonic lethality at implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9501026 10248 Bsg basigin gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20200611 MGI PMID:25891969 10248 Bsg basigin gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20200611 MGI PMID:25891969 10248 Bsg basigin gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20191212 MGI PMID:10967074 10248 Bsg basigin gene MP:0012153 increased b-wave latency IAGP N RGD:5509061 20191212 MGI PMID:10967074 10248 Bsg basigin gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0020216 decreased circulating complement protein level IAGP N RGD:5509061 20200611 MGI PMID:25891969 10248 Bsg basigin gene MP:0020355 abnormal Sertoli cell barrier morphology IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220224 MGI PMID:23727514 10248 Bsg basigin gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:10967074 10250 Nsg1 neuron specific gene family member 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20231207 MGI 10250 Nsg1 neuron specific gene family member 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 10250 Nsg1 neuron specific gene family member 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20231207 MGI 10250 Nsg1 neuron specific gene family member 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20231207 MGI 10250 Nsg1 neuron specific gene family member 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20231207 MGI 10250 Nsg1 neuron specific gene family member 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20231207 MGI 10250 Nsg1 neuron specific gene family member 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 10250 Nsg1 neuron specific gene family member 1 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20221215 MGI 10251 Bsn bassoon gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:12628169 10251 Bsn bassoon gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:12628169 10251 Bsn bassoon gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22933801 10251 Bsn bassoon gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12628169 10251 Bsn bassoon gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:12628169 10251 Bsn bassoon gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12628169 10251 Bsn bassoon gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12628169 10251 Bsn bassoon gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:12628169 10251 Bsn bassoon gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:12628169 10251 Bsn bassoon gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15829963 10251 Bsn bassoon gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:12628169 10251 Bsn bassoon gene MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:15829963 10251 Bsn bassoon gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15829963 10251 Bsn bassoon gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21092861 10251 Bsn bassoon gene MP:0004562 abnormal inner hair cell synaptic ribbon morphology IAGP N RGD:5509061 20141003 MGI PMID:15829963 10251 Bsn bassoon gene MP:0004562 abnormal inner hair cell synaptic ribbon morphology IAGP N RGD:5509061 20141003 MGI PMID:21092861 10251 Bsn bassoon gene MP:0004563 absent active-zone-anchored inner hair cell synaptic ribbon IAGP N RGD:5509061 20141003 MGI PMID:15829963 10251 Bsn bassoon gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15829963 10251 Bsn bassoon gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:15829963 10251 Bsn bassoon gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:12628169 10251 Bsn bassoon gene MP:0005423 abnormal somatic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15829963 10251 Bsn bassoon gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:21092861 10254 Tspo translocator protein gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 10254 Tspo translocator protein gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20160310 MGI PMID:25406832 10254 Tspo translocator protein gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20160310 MGI PMID:25406832 10256 C3 complement component 3 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20180719 MGI PMID:10593909 10256 C3 complement component 3 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20180719 MGI PMID:9367154 10256 C3 complement component 3 gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20180719 MGI PMID:9367154 10256 C3 complement component 3 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20180719 MGI PMID:10066708 10256 C3 complement component 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180719 MGI PMID:19620784 10256 C3 complement component 3 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180719 MGI PMID:19620784 10256 C3 complement component 3 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20180719 MGI PMID:9367154 10256 C3 complement component 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180719 MGI PMID:11801636 10256 C3 complement component 3 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20180719 MGI PMID:21060153 10256 C3 complement component 3 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20180719 MGI PMID:12044978 10256 C3 complement component 3 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20180719 MGI PMID:12044978 10256 C3 complement component 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20180719 MGI PMID:12044978 10256 C3 complement component 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180719 MGI PMID:10698180 10256 C3 complement component 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180719 MGI PMID:12244109 10256 C3 complement component 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180719 MGI PMID:14615480 10256 C3 complement component 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20180719 MGI PMID:26400934 10256 C3 complement component 3 gene MP:0001433 polyphagia IAGP N RGD:5509061 20180719 MGI PMID:10593909 10256 C3 complement component 3 gene MP:0001433 polyphagia IAGP N RGD:5509061 20180719 MGI PMID:10698180 10256 C3 complement component 3 gene MP:0001433 polyphagia IAGP N RGD:5509061 20180719 MGI PMID:12244109 10256 C3 complement component 3 gene MP:0001433 polyphagia IAGP N RGD:5509061 20180719 MGI PMID:14615480 10256 C3 complement component 3 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180719 MGI PMID:10593909 10256 C3 complement component 3 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180719 MGI PMID:10698180 10256 C3 complement component 3 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180719 MGI PMID:12244109 10256 C3 complement component 3 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180719 MGI PMID:14615480 10256 C3 complement component 3 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20180719 MGI PMID:19620784 10256 C3 complement component 3 gene MP:0001657 abnormal induced morbidity/mortality IAGP N RGD:5509061 20180719 MGI PMID:19620784 10256 C3 complement component 3 gene MP:0001661 extended life span IAGP N RGD:5509061 20180719 MGI PMID:12044978 10256 C3 complement component 3 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20180719 MGI PMID:19205046 10256 C3 complement component 3 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20180719 MGI PMID:10698180 10256 C3 complement component 3 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20180719 MGI PMID:11801636 10256 C3 complement component 3 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20180719 MGI PMID:9367154 10256 C3 complement component 3 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20180719 MGI PMID:8752901 10256 C3 complement component 3 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20180719 MGI PMID:12044978 10256 C3 complement component 3 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20180719 MGI PMID:16872848 10256 C3 complement component 3 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20180719 MGI PMID:16778128 10256 C3 complement component 3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180719 MGI PMID:8524789 10256 C3 complement component 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180719 MGI PMID:10593909 10256 C3 complement component 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180719 MGI PMID:10698180 10256 C3 complement component 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180719 MGI PMID:12244109 10256 C3 complement component 3 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180719 MGI PMID:10593909 10256 C3 complement component 3 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180719 MGI PMID:10698180 10256 C3 complement component 3 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180719 MGI PMID:12244109 10256 C3 complement component 3 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20180719 MGI PMID:11801636 10256 C3 complement component 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:9467654 10256 C3 complement component 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190704 MGI PMID:28057640 10256 C3 complement component 3 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20180719 MGI PMID:8752901 10256 C3 complement component 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:10408374 10256 C3 complement component 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:15980239 10256 C3 complement component 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:8524789 10256 C3 complement component 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:9367154 10256 C3 complement component 3 gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20180719 MGI PMID:8524789 10256 C3 complement component 3 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20180719 MGI PMID:9367154 10256 C3 complement component 3 gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20180719 MGI PMID:11986227 10256 C3 complement component 3 gene MP:0002472 impaired complement alternative pathway IAGP N RGD:5509061 20180719 MGI PMID:21943708 10256 C3 complement component 3 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20180719 MGI PMID:12044978 10256 C3 complement component 3 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20180719 MGI PMID:12044978 10256 C3 complement component 3 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20180719 MGI PMID:9409643 10256 C3 complement component 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180719 MGI PMID:19620784 10256 C3 complement component 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180719 MGI PMID:10698180 10256 C3 complement component 3 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20200109 MGI PMID:23074214 10256 C3 complement component 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180719 MGI PMID:10698180 10256 C3 complement component 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180719 MGI PMID:12244109 10256 C3 complement component 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180719 MGI PMID:14615480 10256 C3 complement component 3 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20180719 MGI PMID:9409643 10256 C3 complement component 3 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20180719 MGI PMID:26400934 10256 C3 complement component 3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180719 MGI PMID:19620784 10256 C3 complement component 3 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20180719 MGI PMID:19620784 10256 C3 complement component 3 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20180719 MGI PMID:26400934 10256 C3 complement component 3 gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20180719 MGI PMID:10066708 10256 C3 complement component 3 gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20180719 MGI PMID:18562603 10256 C3 complement component 3 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20180719 MGI PMID:18562603 10256 C3 complement component 3 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20180719 MGI PMID:15048732 10256 C3 complement component 3 gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20180719 MGI PMID:19205046 10256 C3 complement component 3 gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20180719 MGI PMID:12044978 10256 C3 complement component 3 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20180719 MGI PMID:19620784 10256 C3 complement component 3 gene MP:0004031 insulitis IAGP N RGD:5509061 20180719 MGI PMID:17446931 10256 C3 complement component 3 gene MP:0004259 small placenta IAGP N RGD:5509061 20180719 MGI PMID:19205046 10256 C3 complement component 3 gene MP:0004262 abnormal physical strength IAGP N RGD:5509061 20180719 MGI PMID:12044978 10256 C3 complement component 3 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20180719 MGI PMID:11801636 10256 C3 complement component 3 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20180719 MGI PMID:26400934 10256 C3 complement component 3 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20180719 MGI PMID:11801636 10256 C3 complement component 3 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20180719 MGI PMID:17446931 10256 C3 complement component 3 gene MP:0004828 decreased susceptibility to autoimmune hemolytic anemia IAGP N RGD:5509061 20180719 MGI PMID:17317854 10256 C3 complement component 3 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20180719 MGI PMID:26400934 10256 C3 complement component 3 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20180719 MGI PMID:19205046 10256 C3 complement component 3 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20180719 MGI PMID:20709903 10256 C3 complement component 3 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20180719 MGI PMID:16872848 10256 C3 complement component 3 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180719 MGI PMID:10811844 10256 C3 complement component 3 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180719 MGI PMID:17383432 10256 C3 complement component 3 gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20180719 MGI PMID:12244109 10256 C3 complement component 3 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20180719 MGI PMID:10593909 10256 C3 complement component 3 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20180719 MGI PMID:12244109 10256 C3 complement component 3 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20180719 MGI PMID:14615480 10256 C3 complement component 3 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20180719 MGI PMID:19620784 10256 C3 complement component 3 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20180719 MGI PMID:11801636 10256 C3 complement component 3 gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20180719 MGI PMID:14615480 10256 C3 complement component 3 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20180719 MGI PMID:19620784 10256 C3 complement component 3 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:16301611 10256 C3 complement component 3 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:17446931 10256 C3 complement component 3 gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20180719 MGI PMID:11801636 10256 C3 complement component 3 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20180719 MGI PMID:10593909 10256 C3 complement component 3 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20180719 MGI PMID:10698180 10256 C3 complement component 3 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20180719 MGI PMID:12244109 10256 C3 complement component 3 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20180719 MGI PMID:18524992 10256 C3 complement component 3 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20180719 MGI PMID:15240660 10256 C3 complement component 3 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20180719 MGI PMID:19620784 10256 C3 complement component 3 gene MP:0005540 decreased urine albumin level IAGP N RGD:5509061 20180719 MGI PMID:9409643 10256 C3 complement component 3 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20180719 MGI PMID:15980239 10256 C3 complement component 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180719 MGI PMID:10593909 10256 C3 complement component 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180719 MGI PMID:10698180 10256 C3 complement component 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20180719 MGI PMID:10593909 10256 C3 complement component 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20180719 MGI PMID:10698180 10256 C3 complement component 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20180719 MGI PMID:14615480 10256 C3 complement component 3 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20180719 MGI PMID:16778128 10256 C3 complement component 3 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20200109 MGI PMID:23074214 10256 C3 complement component 3 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20200109 MGI PMID:23074214 10256 C3 complement component 3 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20180719 MGI PMID:26400934 10256 C3 complement component 3 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20180719 MGI PMID:26400934 10256 C3 complement component 3 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20180719 MGI PMID:8752901 10256 C3 complement component 3 gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20180719 MGI PMID:8752901 10256 C3 complement component 3 gene MP:0008542 enlarged cervical lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:11801636 10256 C3 complement component 3 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20180719 MGI PMID:19620784 10256 C3 complement component 3 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:17446931 10256 C3 complement component 3 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20180719 MGI PMID:19620784 10256 C3 complement component 3 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20180719 MGI PMID:20709903 10256 C3 complement component 3 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20180719 MGI PMID:9367154 10256 C3 complement component 3 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20180719 MGI PMID:26400934 10256 C3 complement component 3 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20180719 MGI PMID:19205046 10256 C3 complement component 3 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20180719 MGI PMID:19205046 10256 C3 complement component 3 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20180719 MGI PMID:26400934 10256 C3 complement component 3 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20180719 MGI PMID:16872848 10256 C3 complement component 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180719 MGI PMID:9367154 10256 C3 complement component 3 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20180719 MGI PMID:23733878 10256 C3 complement component 3 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20180719 MGI PMID:26400934 10256 C3 complement component 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20180719 MGI PMID:10593909 10256 C3 complement component 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20180719 MGI PMID:10698180 10256 C3 complement component 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20180719 MGI PMID:14615480 10256 C3 complement component 3 gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20180719 MGI PMID:19205046 10256 C3 complement component 3 gene MP:0012040 abnormal c-wave shape IAGP N RGD:5509061 20200109 MGI PMID:23074214 10256 C3 complement component 3 gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20180719 MGI PMID:19205046 10256 C3 complement component 3 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200109 MGI PMID:23074214 10256 C3 complement component 3 gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20180719 MGI PMID:26400934 10256 C3 complement component 3 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20180719 MGI PMID:18562603 10256 C3 complement component 3 gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200625 MGI PMID:30301856 10256 C3 complement component 3 gene MP:0030013 enhanced central nervous system regeneration IAGP N RGD:5509061 20220106 MGI PMID:16936276 10256 C3 complement component 3 gene MP:0031266 decreased susceptibility to alcohol-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:17383432 10258 C4bp complement component 4 binding protein gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 10258 C4bp complement component 4 binding protein gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 10258 C4bp complement component 4 binding protein gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20230119 MGI PMID:28542817 10261 Hc hemolytic complement gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20180719 MGI PMID:25933409 10261 Hc hemolytic complement gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20180719 MGI PMID:10973279 10261 Hc hemolytic complement gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:25933409 10261 Hc hemolytic complement gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:4959665 10261 Hc hemolytic complement gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:9367154 10261 Hc hemolytic complement gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20180719 MGI PMID:25933409 10261 Hc hemolytic complement gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180719 MGI PMID:15995705 10261 Hc hemolytic complement gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20180719 MGI PMID:9485083 10261 Hc hemolytic complement gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20180719 MGI PMID:9485083 10261 Hc hemolytic complement gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180719 MGI PMID:10811844 10261 Hc hemolytic complement gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180719 MGI PMID:17383432 10261 Hc hemolytic complement gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 10261 Hc hemolytic complement gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 10264 C8b complement component 8, beta polypeptide gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:1995474 10264 C8b complement component 8, beta polypeptide gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000333 decreased bone marrow cell number IEA N RGD:5509061 20111116 MGI 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:10611370 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11160387 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000745 tremors IAGP N RGD:5509061 20170713 MGI PMID:21870131 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:4799944 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:18653245 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12023053 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:4799944 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20170713 MGI PMID:21870131 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000851 cerebellum hypoplasia IEA N RGD:5509061 20111116 MGI 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:10611370 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:22279216 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:6123371 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:6167317 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10611370 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22279216 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:23054835 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20170713 MGI PMID:21870131 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20190228 MGI PMID:26730403 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18597946 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22279216 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23054835 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20160818 MGI PMID:22850483 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:22279216 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20170713 MGI PMID:21870131 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:17376154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20190228 MGI PMID:26730403 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20150521 MGI PMID:13950100 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:1486501 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150716 MGI PMID:572084 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10611370 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17146767 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17376154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18597946 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:4799944 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20150521 MGI PMID:13950100 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20111215 MGI 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10611370 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11160387 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12040045 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17146767 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17188510 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17376154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18597946 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19854154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:23054835 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:4799944 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20160818 MGI PMID:22850483 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20170713 MGI PMID:21870131 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:19104150 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17376154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18687887 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17188510 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17376154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18687887 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19104150 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19854154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170713 MGI PMID:21870131 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190228 MGI PMID:26730403 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11160387 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23054835 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001406 abnormal gait IAGP N RGD:5509061 20150521 MGI PMID:13950100 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001406 abnormal gait IAGP N RGD:5509061 20150716 MGI PMID:572084 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:23054835 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:19104150 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001504 abnormal posture IAGP N RGD:5509061 20150521 MGI PMID:13950100 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:18687887 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001513 limb grasping IEA N RGD:5509061 20111116 MGI 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:23054835 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001522 impaired swimming IAGP N RGD:5509061 20150521 MGI PMID:13950100 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10611370 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:17376154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001523 impaired righting response IAGP N RGD:5509061 20170713 MGI PMID:21870131 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:4799944 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20150521 MGI PMID:13950100 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:10611370 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001525 impaired balance IAGP N RGD:5509061 20170713 MGI PMID:21870131 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001525 impaired balance IAGP N RGD:5509061 20190228 MGI PMID:26730403 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001908 abnormal somatosensory cortex physiology IAGP N RGD:5509061 20150716 MGI PMID:25855180 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001921 reduced fertility IAGP N RGD:5509061 20150521 MGI PMID:13950100 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:4799944 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:4799944 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001924 infertility IAGP N RGD:5509061 20150521 MGI PMID:13950100 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001935 decreased litter size IEA N RGD:5509061 20150730 MGI 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:19104150 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:19104150 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002064 seizures IAGP N RGD:5509061 20150521 MGI PMID:13950100 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002064 seizures IAGP N RGD:5509061 20150716 MGI PMID:572084 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:11344116 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:18597946 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:19854154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20150521 MGI PMID:13950100 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:1486501 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10611370 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11344116 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17376154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18597946 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19854154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:11344116 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:11344116 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17146767 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23054835 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:10611370 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12040045 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12151514 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15003170 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:21628556 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18597946 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19104150 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23054835 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20150716 MGI PMID:572084 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002356 abnormal spleen red pulp morphology IEA N RGD:5509061 20111116 MGI 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10611370 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18687887 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21628556 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20150716 MGI PMID:572084 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12040045 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21628556 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:10611370 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15003170 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:12040045 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:22144569 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:11160387 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:18597946 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:19854154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003216 absence seizures IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:11160387 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:11718712 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003481 decreased nerve fiber response intensity IAGP N RGD:5509061 20141003 MGI PMID:11718712 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:10611370 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:11718712 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:15003170 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:18687887 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20160218 MGI PMID:25109669 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003632 abnormal nervous system morphology IEA N RGD:5509061 20111116 MGI 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:11344116 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:1486501 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20150716 MGI PMID:25855180 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20150716 MGI PMID:25855180 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:8229069 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003644 thymus atrophy IEA N RGD:5509061 20111116 MGI 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:17146767 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19854154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11718712 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20170713 MGI PMID:21870131 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20170713 MGI PMID:21870131 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18653245 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20160818 MGI PMID:22850483 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12040045 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:12040045 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:15003170 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0004836 abnormal synaptic acetylcholine release IAGP N RGD:5509061 20141003 MGI PMID:15003170 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0004836 abnormal synaptic acetylcholine release IAGP N RGD:5509061 20141003 MGI PMID:17146767 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:10611370 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:8229069 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:6167317 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:17146767 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:17188510 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:17376154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0005323 dystonia IAGP N RGD:5509061 20160818 MGI PMID:22850483 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:11718712 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:10611370 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:18597946 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11718712 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12023053 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:22144569 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:11160387 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18597946 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22279216 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:23054835 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0008770 decreased survivor rate IEA N RGD:5509061 20150730 MGI 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:10611370 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:19854154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19104150 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0008921 increased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:22279216 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0008925 increased cerebellar granule cell number IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0009357 abnormal seizure response to inducing agent IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:21628556 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19104150 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22144569 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19104150 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:17376154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:21411672 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0010769 abnormal survival IEA N RGD:5509061 20150730 MGI 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17146767 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17188510 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19854154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0011088 neonatal lethality, incomplete penetrance IEA N RGD:5509061 20150730 MGI 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0011090 perinatal lethality, incomplete penetrance IEA N RGD:5509061 20150730 MGI 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18597946 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18597946 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0011267 abnormal excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:22279216 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:12040045 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20181122 MGI PMID:28688851 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0011271 prolonged excitatory postsynaptic current rise time IAGP N RGD:5509061 20240418 MGI PMID:21628556 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0011273 prolonged excitatory postsynaptic current decay time IAGP N RGD:5509061 20240418 MGI PMID:18653245 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0011273 prolonged excitatory postsynaptic current decay time IAGP N RGD:5509061 20240418 MGI PMID:21628556 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20180913 MGI PMID:6123371 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0012590 decreased choline O-acetyltransferase activity IAGP N RGD:5509061 20180927 MGI PMID:6167317 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:12023053 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:17376154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:19854154 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:18597946 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:23054835 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:18597946 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0014331 abnormal Purkinje cell mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:23054835 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0020076 increased brain tyrosine 3-monooxygenase activity IAGP N RGD:5509061 20180927 MGI PMID:6167317 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0030635 increased taurine level IAGP N RGD:5509061 20180913 MGI PMID:6167317 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0030658 increased glycine level IAGP N RGD:5509061 20180913 MGI PMID:6167317 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0030737 decreased glutamic acid level IAGP N RGD:5509061 20180927 MGI PMID:6167317 10265 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene MP:0031202 hemiplegia IAGP N RGD:5509061 20210218 MGI PMID:19104150 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:19429829 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0000692 small spleen IEA N RGD:5509061 20201022 MGI 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20200514 MGI 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17088553 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200514 MGI 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0003488 decreased channel response intensity IAGP N RGD:5509061 20141003 MGI PMID:19429829 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0003489 increased channel response threshold IAGP N RGD:5509061 20141003 MGI PMID:19429829 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19429829 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19429829 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20200514 MGI 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20201022 MGI 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0009453 enhanced contextual conditioning behavior IEA N RGD:5509061 20211021 MGI 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17088553 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20211021 MGI 10269 Cacna2d1 calcium channel, voltage-dependent, alpha2/delta subunit 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:12920136 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:11745616 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0002802 abnormal discrimination learning IAGP N RGD:5509061 20141003 MGI PMID:18339621 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12920136 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12920136 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0002975 vascular smooth muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12920136 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18339621 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0003234 enhanced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18339621 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:9751781 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12920136 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0004267 abnormal optic tract morphology IAGP N RGD:5509061 20141003 MGI PMID:11745616 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17028169 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12920136 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:12920136 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12920136 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12920136 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17028169 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:17028169 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18339621 10270 Cacnb3 calcium channel, voltage-dependent, beta 3 subunit gene MP:0014368 enhanced long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:18339621 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17658952 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:11283268 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20160428 MGI 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160428 MGI 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:11283268 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11283268 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:11283268 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11283268 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:11283268 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:15200417 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18451340 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:18451340 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:15200417 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:11283268 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15200417 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0010173 increased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11283268 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:15200417 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0011419 erythrocyturia IAGP N RGD:5509061 20141003 MGI PMID:15200417 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0011640 abnormal aorta collagen fibril morphology IAGP N RGD:5509061 20160929 MGI PMID:27329311 10271 Ddr1 discoidin domain receptor family, member 1 gene MP:0031391 increased locomotor activity IEA N RGD:5509061 20220421 MGI 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12488435 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12488435 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23047698 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0001562 abnormal circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:12488435 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0001771 abnormal circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:12488435 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0001980 abnormal chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:11276224 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23047698 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22563493 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:12376349 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11717154 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:12488435 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:24121436 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0003929 decreased heart rate variability IAGP N RGD:5509061 20141003 MGI PMID:11717154 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:11717154 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12904337 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0004746 abnormal cochlear IHC afferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12904337 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11717154 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0004878 increased systemic vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:11717154 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:12488435 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:12488435 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:10532808 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10532808 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11276224 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0008715 increased lung small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23047698 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12488435 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10208559 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20141003 MGI PMID:11276224 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0009776 decreased behavioral withdrawal response IAGP N RGD:5509061 20141003 MGI PMID:11276224 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23047698 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0010809 abnormal club cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23047698 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0010918 abnormal pulmonary neuroendocrine body morphology IAGP N RGD:5509061 20141003 MGI PMID:23047698 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0011478 abnormal urine catecholamine level IAGP N RGD:5509061 20141003 MGI PMID:11717154 10274 Calca calcitonin/calcitonin-related polypeptide, alpha gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:24121436 10276 Calcr calcitonin receptor gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:14970190 10276 Calcr calcitonin receptor gene MP:0000202 abnormal circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 10276 Calcr calcitonin receptor gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:18627265 10276 Calcr calcitonin receptor gene MP:0001562 abnormal circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:18627265 10276 Calcr calcitonin receptor gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 10276 Calcr calcitonin receptor gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:18627265 10276 Calcr calcitonin receptor gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:14970190 10276 Calcr calcitonin receptor gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:18627265 10276 Calcr calcitonin receptor gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:14970190 10276 Calcr calcitonin receptor gene MP:0009345 abnormal trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:18627265 10276 Calcr calcitonin receptor gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:18627265 10276 Calcr calcitonin receptor gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:18627265 10276 Calcr calcitonin receptor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18627265 10276 Calcr calcitonin receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12236227 10276 Calcr calcitonin receptor gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:14970190 10278 Calm2 calmodulin 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20240509 MGI PMID:37589122 10278 Calm2 calmodulin 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20240509 MGI PMID:37589122 10278 Calm2 calmodulin 2 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20240509 MGI PMID:37589122 10278 Calm2 calmodulin 2 gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20240509 MGI PMID:37589122 10278 Calm2 calmodulin 2 gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20240509 MGI PMID:37589122 10283 Cetn2 centrin 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20150924 MGI PMID:24790208 10283 Cetn2 centrin 2 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20150924 MGI PMID:24790208 10283 Cetn2 centrin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150924 MGI PMID:24790208 10283 Cetn2 centrin 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20150924 MGI PMID:24790208 10283 Cetn2 centrin 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20150924 MGI PMID:24790208 10283 Cetn2 centrin 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20191114 MGI PMID:30647131 10283 Cetn2 centrin 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20191114 MGI PMID:30647131 10283 Cetn2 centrin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20150924 MGI PMID:24790208 10283 Cetn2 centrin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151112 MGI PMID:24790208 10283 Cetn2 centrin 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20191114 MGI PMID:30647131 10283 Cetn2 centrin 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20191114 MGI PMID:30647131 10283 Cetn2 centrin 2 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20150924 MGI PMID:24790208 10283 Cetn2 centrin 2 gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20191114 MGI PMID:30647131 10283 Cetn2 centrin 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20191114 MGI PMID:30647131 10283 Cetn2 centrin 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20191114 MGI PMID:30647131 10283 Cetn2 centrin 2 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20150924 MGI PMID:24790208 10283 Cetn2 centrin 2 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20191114 MGI PMID:30647131 10283 Cetn2 centrin 2 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20191114 MGI PMID:30647131 10283 Cetn2 centrin 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20191114 MGI PMID:30647131 10283 Cetn2 centrin 2 gene MP:0011281 abnormal olfactory epithelium cilium morphology IAGP N RGD:5509061 20150924 MGI PMID:24790208 10283 Cetn2 centrin 2 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20191114 MGI PMID:30647131 10283 Cetn2 centrin 2 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20191114 MGI PMID:30647131 10283 Cetn2 centrin 2 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20150924 MGI PMID:24790208 10283 Cetn2 centrin 2 gene MP:0013907 abnormal cerebrospinal fluid flow IAGP N RGD:5509061 20150924 MGI PMID:24790208 10283 Cetn2 centrin 2 gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20191114 MGI PMID:30647131 10283 Cetn2 centrin 2 gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20191114 MGI PMID:30647131 10283 Cetn2 centrin 2 gene MP:0020814 abnormal photoreceptor outer segment diameter IAGP N RGD:5509061 20191114 MGI PMID:30647131 10283 Cetn2 centrin 2 gene MP:0030963 abnormal brain ependyma motile cilium location or orientation IAGP N RGD:5509061 20190725 MGI PMID:24790208 10283 Cetn2 centrin 2 gene MP:0030988 dysosmia IAGP N RGD:5509061 20200102 MGI PMID:24790208 10283 Cetn2 centrin 2 gene MP:0030988 dysosmia IAGP N RGD:5509061 20200102 MGI PMID:30647131 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20180802 MGI PMID:18803808 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20180802 MGI PMID:18803808 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:19515929 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0000973 abnormal cutaneous/subcutaneous mechanoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:16875841 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:16875841 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180802 MGI PMID:18803808 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20180802 MGI PMID:18803808 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:1378648 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20180802 MGI PMID:18803808 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20180802 MGI PMID:18803808 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20180802 MGI PMID:27028761 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001394 circling IAGP N RGD:5509061 20190808 MGI PMID:28130356 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19515929 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001399 hyperactivity IAGP N RGD:5509061 20190808 MGI PMID:28130356 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20190808 MGI PMID:28130356 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12408852 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001462 abnormal avoidance learning behavior IAGP N RGD:5509061 20141003 MGI PMID:19515929 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12408851 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12408852 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19515929 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12408851 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12408852 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12408851 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:1378648 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17660813 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19515929 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:7953554 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20161013 MGI PMID:25143599 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:7953554 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:12408851 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20150205 MGI PMID:24485660 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20161013 MGI PMID:25143599 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:12408851 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19515929 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12629219 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:7953554 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20180802 MGI PMID:18803808 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12408851 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12408852 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20190808 MGI PMID:28130356 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20190808 MGI PMID:28130356 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20190808 MGI PMID:28130356 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19515929 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16875841 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:17660813 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:1378648 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17660813 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12629219 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:12408851 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17660813 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20180802 MGI PMID:18803808 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:17660813 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20180802 MGI PMID:18803808 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:17660813 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:8530541 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:16875841 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0008431 abnormal short-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:19515929 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19515929 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20161013 MGI PMID:25143599 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20180802 MGI PMID:18803808 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20180802 MGI PMID:18803808 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20161013 MGI PMID:25143599 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:12408852 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:18803808 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0014413 decreased depression-related behavior IAGP N RGD:5509061 20240425 MGI PMID:18803808 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20190808 MGI PMID:28130356 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20180802 MGI PMID:18803808 10284 Camk2a calcium/calmodulin-dependent protein kinase II alpha gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:18803808 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20151015 MGI PMID:25127391 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20151015 MGI PMID:25127391 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19503086 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0001393 ataxia IAGP N RGD:5509061 20151015 MGI PMID:25127391 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19503086 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0001405 impaired coordination IAGP N RGD:5509061 20151015 MGI PMID:25127391 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20151015 MGI PMID:25127391 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20151015 MGI PMID:25127391 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21752990 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0001525 impaired balance IAGP N RGD:5509061 20151015 MGI PMID:25127391 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:19503086 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19503086 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20181227 MGI 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20151015 MGI PMID:25127391 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:19503086 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20151015 MGI PMID:25127391 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20151015 MGI PMID:25127391 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21752990 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20151015 MGI PMID:25127391 10285 Camk2b calcium/calmodulin-dependent protein kinase II, beta gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 10288 Alx1 ALX homeobox 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0000075 absent neurocranium IAGP N RGD:5509061 20171102 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:15728667 10288 Alx1 ALX homeobox 1 gene MP:0000155 asymmetric rib joints IAGP N RGD:5509061 20141003 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0000445 short snout IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0000449 broad nasal bridge IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0002235 abnormal external nares morphology IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0002778 meroanencephaly IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0003104 acrania IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0003108 short zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0004054 abnormal periocular mesenchyme morphology IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0004339 absent clavicle IAGP N RGD:5509061 20141003 MGI PMID:15728667 10288 Alx1 ALX homeobox 1 gene MP:0004342 scapular bone foramen IAGP N RGD:5509061 20141003 MGI PMID:15728667 10288 Alx1 ALX homeobox 1 gene MP:0004343 small scapula IAGP N RGD:5509061 20141003 MGI PMID:15728667 10288 Alx1 ALX homeobox 1 gene MP:0004347 abnormal scapular spine morphology IAGP N RGD:5509061 20141003 MGI PMID:15728667 10288 Alx1 ALX homeobox 1 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20171102 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0004383 absent interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20171102 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20171102 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0004422 small temporal bone IAGP N RGD:5509061 20171102 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0004441 small occipital bone IAGP N RGD:5509061 20171102 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0004444 small supraoccipital bone IAGP N RGD:5509061 20171102 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0004450 presphenoid bone hypoplasia IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0004459 small alisphenoid bone IAGP N RGD:5509061 20171102 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0004508 abnormal pectoral girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15728667 10288 Alx1 ALX homeobox 1 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20171102 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0004692 small pubis IAGP N RGD:5509061 20141003 MGI PMID:15728667 10288 Alx1 ALX homeobox 1 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15728667 10288 Alx1 ALX homeobox 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0011266 abnormal frontonasal mesenchyme morphology IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20171102 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0012702 increased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0030034 depressed nasal bridge IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0030066 short face IAGP N RGD:5509061 20170921 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20171102 MGI PMID:8673125 10288 Alx1 ALX homeobox 1 gene MP:0030193 short philtrum IAGP N RGD:5509061 20220929 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0030200 abnormal nasal septum cartilage morphology IAGP N RGD:5509061 20171012 MGI PMID:9847249 10288 Alx1 ALX homeobox 1 gene MP:0030833 small acromion IAGP N RGD:5509061 20181018 MGI PMID:15728667 10288 Alx1 ALX homeobox 1 gene MP:0031441 increased periocular mesenchyme apoptosis IAGP N RGD:5509061 20221013 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0031445 midline cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:35127681 10288 Alx1 ALX homeobox 1 gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:8673125 10289 Casp3 caspase 3 gene MP:0000032 cochlear degeneration IAGP N RGD:5509061 20141003 MGI PMID:11251216 10289 Casp3 caspase 3 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:11251216 10289 Casp3 caspase 3 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15599395 10289 Casp3 caspase 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15599395 10289 Casp3 caspase 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21515572 10289 Casp3 caspase 3 gene MP:0000168 abnormal bone marrow development IAGP N RGD:5509061 20141003 MGI PMID:15599395 10289 Casp3 caspase 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15944319 10289 Casp3 caspase 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15831467 10289 Casp3 caspase 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:15156583 10289 Casp3 caspase 3 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16469926 10289 Casp3 caspase 3 gene MP:0000919 cranioschisis IAGP N RGD:5509061 20141003 MGI PMID:15599395 10289 Casp3 caspase 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15994297 10289 Casp3 caspase 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:14985318 10289 Casp3 caspase 3 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:15994297 10289 Casp3 caspase 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:14985318 10289 Casp3 caspase 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15994297 10289 Casp3 caspase 3 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:15994297 10289 Casp3 caspase 3 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:14985318 10289 Casp3 caspase 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21515572 10289 Casp3 caspase 3 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:15599395 10289 Casp3 caspase 3 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:14985318 10289 Casp3 caspase 3 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11062535 10289 Casp3 caspase 3 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14985318 10289 Casp3 caspase 3 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15831467 10289 Casp3 caspase 3 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22195746 10289 Casp3 caspase 3 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:15156583 10289 Casp3 caspase 3 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20141003 MGI PMID:15944319 10289 Casp3 caspase 3 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:15944319 10289 Casp3 caspase 3 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11251216 10289 Casp3 caspase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15156583 10289 Casp3 caspase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15831467 10289 Casp3 caspase 3 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11251216 10289 Casp3 caspase 3 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:15599395 10289 Casp3 caspase 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0002622 abnormal cochlear hair cell morphology IEA N RGD:5509061 20111116 MGI 10289 Casp3 caspase 3 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:15156583 10289 Casp3 caspase 3 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:11251216 10289 Casp3 caspase 3 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:11374883 10289 Casp3 caspase 3 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:15599395 10289 Casp3 caspase 3 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:16469926 10289 Casp3 caspase 3 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15156583 10289 Casp3 caspase 3 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22949508 10289 Casp3 caspase 3 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15994297 10289 Casp3 caspase 3 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22949508 10289 Casp3 caspase 3 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14985318 10289 Casp3 caspase 3 gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:15599395 10289 Casp3 caspase 3 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0004362 cochlear hair cell degeneration IEA N RGD:5509061 20111116 MGI 10289 Casp3 caspase 3 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11251216 10289 Casp3 caspase 3 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11374883 10289 Casp3 caspase 3 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11251216 10289 Casp3 caspase 3 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11374883 10289 Casp3 caspase 3 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:11251216 10289 Casp3 caspase 3 gene MP:0004528 fused outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:11251216 10289 Casp3 caspase 3 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:11374883 10289 Casp3 caspase 3 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15831467 10289 Casp3 caspase 3 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15944319 10289 Casp3 caspase 3 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14985318 10289 Casp3 caspase 3 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16469926 10289 Casp3 caspase 3 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:15944319 10289 Casp3 caspase 3 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:15994297 10289 Casp3 caspase 3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15944319 10289 Casp3 caspase 3 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20160407 MGI PMID:15156583 10289 Casp3 caspase 3 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:11374883 10289 Casp3 caspase 3 gene MP:0006359 absent startle reflex IEA N RGD:5509061 20111116 MGI 10289 Casp3 caspase 3 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15599395 10289 Casp3 caspase 3 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:22949508 10289 Casp3 caspase 3 gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20141003 MGI PMID:14985318 10289 Casp3 caspase 3 gene MP:0008517 thick retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:14985318 10289 Casp3 caspase 3 gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11356696 10289 Casp3 caspase 3 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15831467 10289 Casp3 caspase 3 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:22949508 10289 Casp3 caspase 3 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:16469926 10289 Casp3 caspase 3 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:15599395 10289 Casp3 caspase 3 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16469926 10289 Casp3 caspase 3 gene MP:0009581 decreased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22949508 10289 Casp3 caspase 3 gene MP:0010259 anterior polar cataract IAGP N RGD:5509061 20141003 MGI PMID:15994297 10289 Casp3 caspase 3 gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:15944319 10289 Casp3 caspase 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16469926 10289 Casp3 caspase 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16469926 10289 Casp3 caspase 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15156583 10289 Casp3 caspase 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21515572 10289 Casp3 caspase 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8934524 10289 Casp3 caspase 3 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:11251216 10289 Casp3 caspase 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11251216 10289 Casp3 caspase 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11374883 10289 Casp3 caspase 3 gene MP:0012260 encephalomeningocele IAGP N RGD:5509061 20141003 MGI PMID:21515572 10289 Casp3 caspase 3 gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16469926 10289 Casp3 caspase 3 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:14985318 10289 Casp3 caspase 3 gene MP:0030263 cranial bossing IEA N RGD:5509061 20171123 MGI 10289 Casp3 caspase 3 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:11356696 10292 Cast calpastatin gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20240523 MGI 10292 Cast calpastatin gene MP:0000604 amyloidosis IAGP N RGD:5509061 20150618 MGI PMID:24728269 10292 Cast calpastatin gene MP:0001406 abnormal gait IEA N RGD:5509061 20240523 MGI 10292 Cast calpastatin gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20160421 MGI 10292 Cast calpastatin gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20160421 MGI 10292 Cast calpastatin gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21791606 10292 Cast calpastatin gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20150618 MGI PMID:24728269 10292 Cast calpastatin gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20240523 MGI 10292 Cast calpastatin gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 10292 Cast calpastatin gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 10292 Cast calpastatin gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20150618 MGI PMID:24728269 10292 Cast calpastatin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20150618 MGI PMID:24728269 10292 Cast calpastatin gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 10292 Cast calpastatin gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:15691848 10292 Cast calpastatin gene MP:0008918 microgliosis IAGP N RGD:5509061 20150618 MGI PMID:24728269 10292 Cast calpastatin gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:21791606 10292 Cast calpastatin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21791606 10292 Cast calpastatin gene MP:0012000 abnormal limb position IEA N RGD:5509061 20240523 MGI 10297 Cbs cystathionine beta-synthase gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0000160 kyphosis IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20161020 MGI PMID:19858416 10297 Cbs cystathionine beta-synthase gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0000448 pointed snout IAGP N RGD:5509061 20141003 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0000585 kinked tail IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0000592 short tail IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20638879 10297 Cbs cystathionine beta-synthase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0001237 enlarged spinous cells IAGP N RGD:5509061 20141003 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161020 MGI PMID:19858416 10297 Cbs cystathionine beta-synthase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0001265 decreased body size IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:10993757 10297 Cbs cystathionine beta-synthase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15887121 10297 Cbs cystathionine beta-synthase gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16984962 10297 Cbs cystathionine beta-synthase gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:16984962 10297 Cbs cystathionine beta-synthase gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15887121 10297 Cbs cystathionine beta-synthase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20638879 10297 Cbs cystathionine beta-synthase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15887121 10297 Cbs cystathionine beta-synthase gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0002764 short tibia IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0003109 short femur IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15887121 10297 Cbs cystathionine beta-synthase gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:15887121 10297 Cbs cystathionine beta-synthase gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20240502 MGI PMID:22617046 10297 Cbs cystathionine beta-synthase gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15887121 10297 Cbs cystathionine beta-synthase gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10993757 10297 Cbs cystathionine beta-synthase gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:16984962 10297 Cbs cystathionine beta-synthase gene MP:0004125 abnormal venule morphology IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0004126 thin hypodermis IAGP N RGD:5509061 20141003 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16984962 10297 Cbs cystathionine beta-synthase gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20240502 MGI PMID:22617046 10297 Cbs cystathionine beta-synthase gene MP:0004351 short humerus IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0004359 short ulna IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0004610 small vertebrae IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0004903 abnormal uterus weight IAGP N RGD:5509061 20141003 MGI PMID:16984962 10297 Cbs cystathionine beta-synthase gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:16984962 10297 Cbs cystathionine beta-synthase gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20240502 MGI PMID:22617046 10297 Cbs cystathionine beta-synthase gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:16984962 10297 Cbs cystathionine beta-synthase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:20566639 10297 Cbs cystathionine beta-synthase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:20638879 10297 Cbs cystathionine beta-synthase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:19204075 10297 Cbs cystathionine beta-synthase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20180913 MGI PMID:15887121 10297 Cbs cystathionine beta-synthase gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20161020 MGI PMID:19858416 10297 Cbs cystathionine beta-synthase gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:20638879 10297 Cbs cystathionine beta-synthase gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0006076 abnormal circulating homocysteine level IAGP N RGD:5509061 20141003 MGI PMID:19204075 10297 Cbs cystathionine beta-synthase gene MP:0006076 abnormal circulating homocysteine level IAGP N RGD:5509061 20141003 MGI PMID:20638879 10297 Cbs cystathionine beta-synthase gene MP:0006076 abnormal circulating homocysteine level IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0006190 retina ischemia IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0006296 arachnodactyly IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0008047 absent uterine NK cells IAGP N RGD:5509061 20240502 MGI PMID:22617046 10297 Cbs cystathionine beta-synthase gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20161020 MGI PMID:19858416 10297 Cbs cystathionine beta-synthase gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:15887121 10297 Cbs cystathionine beta-synthase gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15887121 10297 Cbs cystathionine beta-synthase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:20638879 10297 Cbs cystathionine beta-synthase gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:16984962 10297 Cbs cystathionine beta-synthase gene MP:0008876 decreased uterine NK cell number IAGP N RGD:5509061 20240502 MGI PMID:22617046 10297 Cbs cystathionine beta-synthase gene MP:0008957 abnormal placenta junctional zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16984962 10297 Cbs cystathionine beta-synthase gene MP:0009007 short estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:16984962 10297 Cbs cystathionine beta-synthase gene MP:0009012 short diestrus IAGP N RGD:5509061 20141003 MGI PMID:16984962 10297 Cbs cystathionine beta-synthase gene MP:0009018 short estrus IAGP N RGD:5509061 20141003 MGI PMID:16984962 10297 Cbs cystathionine beta-synthase gene MP:0009020 prolonged metestrus IAGP N RGD:5509061 20141003 MGI PMID:16984962 10297 Cbs cystathionine beta-synthase gene MP:0009392 retina gliosis IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20638879 10297 Cbs cystathionine beta-synthase gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:16984962 10297 Cbs cystathionine beta-synthase gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20240502 MGI PMID:22617046 10297 Cbs cystathionine beta-synthase gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0010452 retina microaneurysm IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0011520 increased placental labyrinth size IAGP N RGD:5509061 20240502 MGI PMID:16984962 10297 Cbs cystathionine beta-synthase gene MP:0012065 increased astrocyte number IAGP N RGD:5509061 20141030 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0012110 increased hair follicle number IAGP N RGD:5509061 20181129 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20161020 MGI PMID:19204075 10297 Cbs cystathionine beta-synthase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20161020 MGI PMID:19858416 10297 Cbs cystathionine beta-synthase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20180913 MGI PMID:15386278 10297 Cbs cystathionine beta-synthase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20180913 MGI PMID:20566639 10297 Cbs cystathionine beta-synthase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20180913 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20180920 MGI PMID:10993757 10297 Cbs cystathionine beta-synthase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20220616 MGI PMID:15622513 10297 Cbs cystathionine beta-synthase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20240502 MGI PMID:22617046 10297 Cbs cystathionine beta-synthase gene MP:0012602 increased alpha-fetoprotein level IAGP N RGD:5509061 20240502 MGI PMID:22617046 10297 Cbs cystathionine beta-synthase gene MP:0013022 increased Ly6C high monocyte number IAGP N RGD:5509061 20161020 MGI PMID:19858416 10297 Cbs cystathionine beta-synthase gene MP:0014179 abnormal blood-retina barrier function IAGP N RGD:5509061 20160526 MGI PMID:25016930 10297 Cbs cystathionine beta-synthase gene MP:0030639 decreased circulating taurine level IAGP N RGD:5509061 20180913 MGI PMID:20566639 10297 Cbs cystathionine beta-synthase gene MP:0030644 increased circulating methionine level IAGP N RGD:5509061 20180920 MGI PMID:19858416 10297 Cbs cystathionine beta-synthase gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:7878023 10297 Cbs cystathionine beta-synthase gene MP:0031214 hypercoagulability IAGP N RGD:5509061 20201231 MGI PMID:20638879 10298 Cck cholecystokinin gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20161201 MGI 10298 Cck cholecystokinin gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:10330022 10298 Cck cholecystokinin gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:10330022 10298 Cck cholecystokinin gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20111116 MGI 10299 Cckar cholecystokinin A receptor gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15152034 10299 Cckar cholecystokinin A receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11925470 10299 Cckar cholecystokinin A receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12459512 10299 Cckar cholecystokinin A receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15168241 10299 Cckar cholecystokinin A receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15178543 10299 Cckar cholecystokinin A receptor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12459512 10299 Cckar cholecystokinin A receptor gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:11925470 10299 Cckar cholecystokinin A receptor gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15178543 10299 Cckar cholecystokinin A receptor gene MP:0002646 increased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:15314689 10299 Cckar cholecystokinin A receptor gene MP:0002694 abnormal pancreas secretion IAGP N RGD:5509061 20141003 MGI PMID:11893936 10299 Cckar cholecystokinin A receptor gene MP:0002830 gallstones IAGP N RGD:5509061 20141003 MGI PMID:15314689 10299 Cckar cholecystokinin A receptor gene MP:0002830 gallstones IAGP N RGD:5509061 20141003 MGI PMID:9927499 10299 Cckar cholecystokinin A receptor gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:11925470 10299 Cckar cholecystokinin A receptor gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:18305161 10299 Cckar cholecystokinin A receptor gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:18305161 10299 Cckar cholecystokinin A receptor gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:15314689 10299 Cckar cholecystokinin A receptor gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:11925470 10299 Cckar cholecystokinin A receptor gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:12459512 10299 Cckar cholecystokinin A receptor gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:18305161 10299 Cckar cholecystokinin A receptor gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15314689 10299 Cckar cholecystokinin A receptor gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 10299 Cckar cholecystokinin A receptor gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15314689 10299 Cckar cholecystokinin A receptor gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:9927499 10299 Cckar cholecystokinin A receptor gene MP:0006002 abnormal small intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:15314689 10299 Cckar cholecystokinin A receptor gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:15152034 10299 Cckar cholecystokinin A receptor gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18305161 10299 Cckar cholecystokinin A receptor gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:11925470 10299 Cckar cholecystokinin A receptor gene MP:0009854 impaired gastric peristalsis IAGP N RGD:5509061 20141003 MGI PMID:15168241 10299 Cckar cholecystokinin A receptor gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20190502 MGI 10299 Cckar cholecystokinin A receptor gene MP:0020132 increased gallbladder volume IAGP N RGD:5509061 20200116 MGI PMID:15314689 10300 Cckbr cholecystokinin B receptor gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20200514 MGI 10300 Cckbr cholecystokinin B receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11925470 10300 Cckbr cholecystokinin B receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12459512 10300 Cckbr cholecystokinin B receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15168241 10300 Cckbr cholecystokinin B receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15178543 10300 Cckbr cholecystokinin B receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15325774 10300 Cckbr cholecystokinin B receptor gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12459512 10300 Cckbr cholecystokinin B receptor gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15013032 10300 Cckbr cholecystokinin B receptor gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15325774 10300 Cckbr cholecystokinin B receptor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11403953 10300 Cckbr cholecystokinin B receptor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11682252 10300 Cckbr cholecystokinin B receptor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16857893 10300 Cckbr cholecystokinin B receptor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11682252 10300 Cckbr cholecystokinin B receptor gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:11925470 10300 Cckbr cholecystokinin B receptor gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:15325774 10300 Cckbr cholecystokinin B receptor gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:8876222 10300 Cckbr cholecystokinin B receptor gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15178543 10300 Cckbr cholecystokinin B receptor gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:15355324 10300 Cckbr cholecystokinin B receptor gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:8876222 10300 Cckbr cholecystokinin B receptor gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:15355324 10300 Cckbr cholecystokinin B receptor gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20392936 10300 Cckbr cholecystokinin B receptor gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20141003 MGI PMID:16857893 10300 Cckbr cholecystokinin B receptor gene MP:0003892 abnormal gastric gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8978369 10300 Cckbr cholecystokinin B receptor gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:11925470 10300 Cckbr cholecystokinin B receptor gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8978369 10300 Cckbr cholecystokinin B receptor gene MP:0004152 abnormal circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:18755804 10300 Cckbr cholecystokinin B receptor gene MP:0004731 increased circulating gastrin level IAGP N RGD:5509061 20141003 MGI PMID:15168241 10300 Cckbr cholecystokinin B receptor gene MP:0004731 increased circulating gastrin level IAGP N RGD:5509061 20141003 MGI PMID:18755804 10300 Cckbr cholecystokinin B receptor gene MP:0004731 increased circulating gastrin level IAGP N RGD:5509061 20141003 MGI PMID:8876222 10300 Cckbr cholecystokinin B receptor gene MP:0004731 increased circulating gastrin level IAGP N RGD:5509061 20141003 MGI PMID:8978369 10300 Cckbr cholecystokinin B receptor gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:11925470 10300 Cckbr cholecystokinin B receptor gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:11682252 10300 Cckbr cholecystokinin B receptor gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:12459512 10300 Cckbr cholecystokinin B receptor gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:15325774 10300 Cckbr cholecystokinin B receptor gene MP:0005218 abnormal pancreatic delta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8978369 10300 Cckbr cholecystokinin B receptor gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:15355324 10300 Cckbr cholecystokinin B receptor gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20141003 MGI PMID:8978369 10300 Cckbr cholecystokinin B receptor gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16857893 10300 Cckbr cholecystokinin B receptor gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:18755804 10300 Cckbr cholecystokinin B receptor gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11403953 10300 Cckbr cholecystokinin B receptor gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:11925470 10300 Cckbr cholecystokinin B receptor gene MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:11403953 10300 Cckbr cholecystokinin B receptor gene MP:0009753 enhanced behavioral response to morphine IAGP N RGD:5509061 20141003 MGI PMID:11403953 10300 Cckbr cholecystokinin B receptor gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:11403953 10300 Cckbr cholecystokinin B receptor gene MP:0009854 impaired gastric peristalsis IAGP N RGD:5509061 20141003 MGI PMID:15168241 10300 Cckbr cholecystokinin B receptor gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:8876222 10300 Cckbr cholecystokinin B receptor gene MP:0010803 abnormal stomach enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8978369 10300 Cckbr cholecystokinin B receptor gene MP:0011891 decreased circulating ferritin level IAGP N RGD:5509061 20141003 MGI PMID:18755804 10300 Cckbr cholecystokinin B receptor gene MP:0011897 decreased circulating unsaturated transferrin level IAGP N RGD:5509061 20141003 MGI PMID:18755804 10300 Cckbr cholecystokinin B receptor gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:16857893 10300 Cckbr cholecystokinin B receptor gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:16857893 10304 Cd2 CD2 antigen gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:1358605 10306 Cd24a CD24a antigen gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9028339 10306 Cd24a CD24a antigen gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9028339 10306 Cd24a CD24a antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9028339 10306 Cd24a CD24a antigen gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:9028339 10306 Cd24a CD24a antigen gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9028339 10306 Cd24a CD24a antigen gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:9028339 10306 Cd24a CD24a antigen gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9028339 10306 Cd24a CD24a antigen gene MP:0010035 increased erythrocyte clearance IAGP N RGD:5509061 20200618 MGI PMID:9028339 10306 Cd24a CD24a antigen gene MP:0020455 increased erythrocyte aggregation IAGP N RGD:5509061 20170914 MGI PMID:9028339 10306 Cd24a CD24a antigen gene MP:0031063 increased erythrocyte sedimentation rate IAGP N RGD:5509061 20200618 MGI PMID:9028339 10306 Cd24a CD24a antigen gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:9028339 10307 Cd28 CD28 antigen gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20160804 MGI 10307 Cd28 CD28 antigen gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:23281398 10307 Cd28 CD28 antigen gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:23281398 10307 Cd28 CD28 antigen gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23851689 10307 Cd28 CD28 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23281398 10307 Cd28 CD28 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23281398 10307 Cd28 CD28 antigen gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:23793062 10307 Cd28 CD28 antigen gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:23281398 10307 Cd28 CD28 antigen gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:23281398 10307 Cd28 CD28 antigen gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23281398 10307 Cd28 CD28 antigen gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:23281398 10307 Cd28 CD28 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12752681 10307 Cd28 CD28 antigen gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:7751626 10307 Cd28 CD28 antigen gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:18097000 10307 Cd28 CD28 antigen gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:23281398 10307 Cd28 CD28 antigen gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:10477557 10307 Cd28 CD28 antigen gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22700722 10307 Cd28 CD28 antigen gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10725709 10307 Cd28 CD28 antigen gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19398586 10307 Cd28 CD28 antigen gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16908623 10307 Cd28 CD28 antigen gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16908623 10307 Cd28 CD28 antigen gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:7688139 10307 Cd28 CD28 antigen gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12752681 10307 Cd28 CD28 antigen gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16908623 10307 Cd28 CD28 antigen gene MP:0003278 esophageal inflammation IAGP N RGD:5509061 20141003 MGI PMID:23851689 10307 Cd28 CD28 antigen gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:7751626 10307 Cd28 CD28 antigen gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:15467837 10307 Cd28 CD28 antigen gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:10528184 10307 Cd28 CD28 antigen gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:11285307 10307 Cd28 CD28 antigen gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:12070288 10307 Cd28 CD28 antigen gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:23281398 10307 Cd28 CD28 antigen gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:10477557 10307 Cd28 CD28 antigen gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:19398586 10307 Cd28 CD28 antigen gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:15467837 10307 Cd28 CD28 antigen gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:8808683 10307 Cd28 CD28 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:12752681 10307 Cd28 CD28 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:15024044 10307 Cd28 CD28 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:7688139 10307 Cd28 CD28 antigen gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23065717 10307 Cd28 CD28 antigen gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:23281398 10307 Cd28 CD28 antigen gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:15467837 10307 Cd28 CD28 antigen gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23065717 10307 Cd28 CD28 antigen gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23281398 10307 Cd28 CD28 antigen gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23793062 10307 Cd28 CD28 antigen gene MP:0005002 abnormal T cell clonal deletion IAGP N RGD:5509061 20141003 MGI PMID:11342622 10307 Cd28 CD28 antigen gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17873878 10307 Cd28 CD28 antigen gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23851689 10307 Cd28 CD28 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23281398 10307 Cd28 CD28 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9075933 10307 Cd28 CD28 antigen gene MP:0005018 decreased T cell number IEA N RGD:5509061 20141003 MGI 10307 Cd28 CD28 antigen gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15213110 10307 Cd28 CD28 antigen gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10528184 10307 Cd28 CD28 antigen gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12752681 10307 Cd28 CD28 antigen gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:15024044 10307 Cd28 CD28 antigen gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7751626 10307 Cd28 CD28 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11285307 10307 Cd28 CD28 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15024044 10307 Cd28 CD28 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16908623 10307 Cd28 CD28 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18097000 10307 Cd28 CD28 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19398586 10307 Cd28 CD28 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23281398 10307 Cd28 CD28 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23793062 10307 Cd28 CD28 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7688139 10307 Cd28 CD28 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8808683 10307 Cd28 CD28 antigen gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15467837 10307 Cd28 CD28 antigen gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:17873878 10307 Cd28 CD28 antigen gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:23281398 10307 Cd28 CD28 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10795741 10307 Cd28 CD28 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7688139 10307 Cd28 CD28 antigen gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:8808683 10307 Cd28 CD28 antigen gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:8808683 10307 Cd28 CD28 antigen gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:19398586 10307 Cd28 CD28 antigen gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:12752681 10307 Cd28 CD28 antigen gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:10795741 10307 Cd28 CD28 antigen gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19398586 10307 Cd28 CD28 antigen gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18097000 10307 Cd28 CD28 antigen gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11342622 10307 Cd28 CD28 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11285307 10307 Cd28 CD28 antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11342622 10307 Cd28 CD28 antigen gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16908623 10307 Cd28 CD28 antigen gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:15024044 10307 Cd28 CD28 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12752681 10307 Cd28 CD28 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:7688139 10307 Cd28 CD28 antigen gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12752681 10307 Cd28 CD28 antigen gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:8808683 10307 Cd28 CD28 antigen gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:7688139 10307 Cd28 CD28 antigen gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:7688139 10307 Cd28 CD28 antigen gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:8808683 10307 Cd28 CD28 antigen gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23793062 10307 Cd28 CD28 antigen gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:11285307 10307 Cd28 CD28 antigen gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:15629449 10307 Cd28 CD28 antigen gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:15629449 10307 Cd28 CD28 antigen gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:12752681 10307 Cd28 CD28 antigen gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:23851689 10307 Cd28 CD28 antigen gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:11285307 10307 Cd28 CD28 antigen gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:16908623 10307 Cd28 CD28 antigen gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:18097000 10307 Cd28 CD28 antigen gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19398586 10307 Cd28 CD28 antigen gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:23793062 10307 Cd28 CD28 antigen gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:7688139 10307 Cd28 CD28 antigen gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:7751626 10307 Cd28 CD28 antigen gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:8808683 10307 Cd28 CD28 antigen gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:23851689 10307 Cd28 CD28 antigen gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:8808683 10307 Cd28 CD28 antigen gene MP:0008747 abnormal T cell anergy IAGP N RGD:5509061 20141003 MGI PMID:15024044 10307 Cd28 CD28 antigen gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:11285307 10307 Cd28 CD28 antigen gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12752681 10307 Cd28 CD28 antigen gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15024044 10307 Cd28 CD28 antigen gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12752681 10307 Cd28 CD28 antigen gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22700722 10307 Cd28 CD28 antigen gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15629449 10308 Cd247 CD247 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:8223495 10308 Cd247 CD247 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8223495 10308 Cd247 CD247 antigen gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:8223495 10308 Cd247 CD247 antigen gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22945921 10308 Cd247 CD247 antigen gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:7688481 10308 Cd247 CD247 antigen gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8223444 10308 Cd247 CD247 antigen gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8223445 10308 Cd247 CD247 antigen gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8223495 10308 Cd247 CD247 antigen gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:9529325 10308 Cd247 CD247 antigen gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:11118151 10308 Cd247 CD247 antigen gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:11118151 10308 Cd247 CD247 antigen gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8223495 10308 Cd247 CD247 antigen gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:9529325 10308 Cd247 CD247 antigen gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:11118151 10308 Cd247 CD247 antigen gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:11118151 10308 Cd247 CD247 antigen gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15878887 10308 Cd247 CD247 antigen gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10072519 10308 Cd247 CD247 antigen gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22945921 10308 Cd247 CD247 antigen gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7520000 10308 Cd247 CD247 antigen gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8223444 10308 Cd247 CD247 antigen gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8223495 10308 Cd247 CD247 antigen gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:11118151 10308 Cd247 CD247 antigen gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22945921 10308 Cd247 CD247 antigen gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11118151 10308 Cd247 CD247 antigen gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10072519 10308 Cd247 CD247 antigen gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7520000 10308 Cd247 CD247 antigen gene MP:0002433 abnormal T-helper 1 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7688481 10308 Cd247 CD247 antigen gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9529325 10308 Cd247 CD247 antigen gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22945921 10308 Cd247 CD247 antigen gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:11118151 10308 Cd247 CD247 antigen gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11118151 10308 Cd247 CD247 antigen gene MP:0003080 increased natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11123272 10308 Cd247 CD247 antigen gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:10072519 10308 Cd247 CD247 antigen gene MP:0004165 abnormal lateral geniculate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11118151 10308 Cd247 CD247 antigen gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15878887 10308 Cd247 CD247 antigen gene MP:0004260 enlarged placenta IAGP N RGD:5509061 20141003 MGI PMID:15878887 10308 Cd247 CD247 antigen gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:22945921 10308 Cd247 CD247 antigen gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22945921 10308 Cd247 CD247 antigen gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22945921 10308 Cd247 CD247 antigen gene MP:0005068 abnormal NK cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11123272 10308 Cd247 CD247 antigen gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11021533 10308 Cd247 CD247 antigen gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:8223444 10308 Cd247 CD247 antigen gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:8223495 10308 Cd247 CD247 antigen gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10072519 10308 Cd247 CD247 antigen gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:7688481 10308 Cd247 CD247 antigen gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8223444 10308 Cd247 CD247 antigen gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8223445 10308 Cd247 CD247 antigen gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8223495 10308 Cd247 CD247 antigen gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8223445 10308 Cd247 CD247 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8223495 10308 Cd247 CD247 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IEA N RGD:5509061 20111208 MGI 10308 Cd247 CD247 antigen gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:9529325 10308 Cd247 CD247 antigen gene MP:0008036 abnormal NK T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22945921 10308 Cd247 CD247 antigen gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10072519 10308 Cd247 CD247 antigen gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:7650493 10308 Cd247 CD247 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22945921 10308 Cd247 CD247 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:7688481 10308 Cd247 CD247 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8223444 10308 Cd247 CD247 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8223445 10308 Cd247 CD247 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8223495 10308 Cd247 CD247 antigen gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22945921 10308 Cd247 CD247 antigen gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8223444 10308 Cd247 CD247 antigen gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8223445 10308 Cd247 CD247 antigen gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8223495 10308 Cd247 CD247 antigen gene MP:0008081 abnormal single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:7688481 10308 Cd247 CD247 antigen gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8223444 10308 Cd247 CD247 antigen gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8223445 10308 Cd247 CD247 antigen gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22945921 10308 Cd247 CD247 antigen gene MP:0008352 absent gamma-delta intraepithelial T cell IAGP N RGD:5509061 20141003 MGI PMID:9529325 10308 Cd247 CD247 antigen gene MP:0008356 abnormal gamma-delta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22945921 10308 Cd247 CD247 antigen gene MP:0008399 abnormal alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8223445 10308 Cd247 CD247 antigen gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:11118151 10308 Cd247 CD247 antigen gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11123272 10308 Cd247 CD247 antigen gene MP:0008876 decreased uterine NK cell number IAGP N RGD:5509061 20141003 MGI PMID:15878887 10308 Cd247 CD247 antigen gene MP:0008894 abnormal intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8223444 10308 Cd247 CD247 antigen gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22945921 10308 Cd247 CD247 antigen gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:8223495 10308 Cd247 CD247 antigen gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22945921 10308 Cd247 CD247 antigen gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11123272 10308 Cd247 CD247 antigen gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8131747 10308 Cd247 CD247 antigen gene MP:0012529 abnormal decidua basalis morphology IAGP N RGD:5509061 20141003 MGI PMID:15878887 10308 Cd247 CD247 antigen gene MP:0012726 abnormal uterine spiral artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15878887 10308 Cd247 CD247 antigen gene MP:0012727 abnormal uterine spiral artery remodeling IAGP N RGD:5509061 20141003 MGI PMID:15878887 10308 Cd247 CD247 antigen gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:8223445 10308 Cd247 CD247 antigen gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:8223495 10308 Cd247 CD247 antigen gene MP:0013593 enlarged thymus cortex IAGP N RGD:5509061 20150319 MGI PMID:8223495 10309 Cd4 CD4 antigen gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9521047 10309 Cd4 CD4 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7930593 10309 Cd4 CD4 antigen gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9551897 10309 Cd4 CD4 antigen gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:9696828 10309 Cd4 CD4 antigen gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:11114377 10309 Cd4 CD4 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:9521047 10309 Cd4 CD4 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9521047 10309 Cd4 CD4 antigen gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:9696828 10309 Cd4 CD4 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12486099 10309 Cd4 CD4 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15922720 10309 Cd4 CD4 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7930593 10309 Cd4 CD4 antigen gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8500525 10309 Cd4 CD4 antigen gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9551897 10309 Cd4 CD4 antigen gene MP:0002347 abnormal lymph node T cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:9521047 10309 Cd4 CD4 antigen gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8500525 10309 Cd4 CD4 antigen gene MP:0002408 abnormal double-positive T cell morphology IEA N RGD:5509061 20220106 MGI 10309 Cd4 CD4 antigen gene MP:0002418 increased susceptibility to viral infection IAGP N RGD:5509061 20141003 MGI PMID:7676644 10309 Cd4 CD4 antigen gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IEA N RGD:5509061 20220106 MGI 10309 Cd4 CD4 antigen gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22036949 10309 Cd4 CD4 antigen gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9521047 10309 Cd4 CD4 antigen gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:7930593 10309 Cd4 CD4 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:7930593 10309 Cd4 CD4 antigen gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:7930593 10309 Cd4 CD4 antigen gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:9521047 10309 Cd4 CD4 antigen gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:7930593 10309 Cd4 CD4 antigen gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:12486099 10309 Cd4 CD4 antigen gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:8467804 10309 Cd4 CD4 antigen gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:9521047 10309 Cd4 CD4 antigen gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:8500525 10309 Cd4 CD4 antigen gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:19017966 10309 Cd4 CD4 antigen gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:17202343 10309 Cd4 CD4 antigen gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20210318 MGI PMID:33238133 10309 Cd4 CD4 antigen gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10725754 10309 Cd4 CD4 antigen gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10725754 10309 Cd4 CD4 antigen gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19668367 10309 Cd4 CD4 antigen gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:24115907 10309 Cd4 CD4 antigen gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7930593 10309 Cd4 CD4 antigen gene MP:0005018 decreased T cell number IEA N RGD:5509061 20111116 MGI 10309 Cd4 CD4 antigen gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:14688093 10309 Cd4 CD4 antigen gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:8500525 10309 Cd4 CD4 antigen gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:8671660 10309 Cd4 CD4 antigen gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8500525 10309 Cd4 CD4 antigen gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9551897 10309 Cd4 CD4 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11748274 10309 Cd4 CD4 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8467804 10309 Cd4 CD4 antigen gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11748274 10309 Cd4 CD4 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11748274 10309 Cd4 CD4 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:1832488 10309 Cd4 CD4 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8467804 10309 Cd4 CD4 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8671660 10309 Cd4 CD4 antigen gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:11748274 10309 Cd4 CD4 antigen gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:8500525 10309 Cd4 CD4 antigen gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:9551897 10309 Cd4 CD4 antigen gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11748274 10309 Cd4 CD4 antigen gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:24115907 10309 Cd4 CD4 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11748274 10309 Cd4 CD4 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14688093 10309 Cd4 CD4 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20360383 10309 Cd4 CD4 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9551897 10309 Cd4 CD4 antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11748274 10309 Cd4 CD4 antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14688093 10309 Cd4 CD4 antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1832488 10309 Cd4 CD4 antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20360383 10309 Cd4 CD4 antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8467804 10309 Cd4 CD4 antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9521047 10309 Cd4 CD4 antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9551897 10309 Cd4 CD4 antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20210318 MGI PMID:33238133 10309 Cd4 CD4 antigen gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20210318 MGI PMID:33238133 10309 Cd4 CD4 antigen gene MP:0008087 decreased T helper 1 cell number IAGP N RGD:5509061 20230316 MGI PMID:35304452 10309 Cd4 CD4 antigen gene MP:0008100 absent plasma cells IAGP N RGD:5509061 20141003 MGI PMID:17202343 10309 Cd4 CD4 antigen gene MP:0008345 abnormal gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8500525 10309 Cd4 CD4 antigen gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:7930593 10309 Cd4 CD4 antigen gene MP:0008698 abnormal interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:11748274 10309 Cd4 CD4 antigen gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:7930593 10309 Cd4 CD4 antigen gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:7930593 10309 Cd4 CD4 antigen gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20210318 MGI PMID:33238133 10309 Cd4 CD4 antigen gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:8500525 10309 Cd4 CD4 antigen gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20141003 MGI 10309 Cd4 CD4 antigen gene MP:0020191 abnormal lymphocyte activation involved in immune response IAGP N RGD:5509061 20230316 MGI PMID:35304452 10309 Cd4 CD4 antigen gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:9696828 10310 Cd44 CD44 antigen gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:19204665 10310 Cd44 CD44 antigen gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:18250474 10310 Cd44 CD44 antigen gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15126101 10310 Cd44 CD44 antigen gene MP:0000362 decreased mast cell histamine storage IAGP N RGD:5509061 20141003 MGI PMID:19204665 10310 Cd44 CD44 antigen gene MP:0000414 alopecia IEA N RGD:5509061 20200430 MGI 10310 Cd44 CD44 antigen gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17923692 10310 Cd44 CD44 antigen gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:11825873 10310 Cd44 CD44 antigen gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:16557236 10310 Cd44 CD44 antigen gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10859330 10310 Cd44 CD44 antigen gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16061657 10310 Cd44 CD44 antigen gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:11956084 10310 Cd44 CD44 antigen gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:16557236 10310 Cd44 CD44 antigen gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:16816384 10310 Cd44 CD44 antigen gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:10859330 10310 Cd44 CD44 antigen gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:10859330 10310 Cd44 CD44 antigen gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:18250474 10310 Cd44 CD44 antigen gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:11935029 10310 Cd44 CD44 antigen gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11342603 10310 Cd44 CD44 antigen gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:11935029 10310 Cd44 CD44 antigen gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12466136 10310 Cd44 CD44 antigen gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17923692 10310 Cd44 CD44 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23318432 10310 Cd44 CD44 antigen gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20180712 MGI PMID:22834956 10310 Cd44 CD44 antigen gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9310473 10310 Cd44 CD44 antigen gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 10310 Cd44 CD44 antigen gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20150326 MGI PMID:23318432 10310 Cd44 CD44 antigen gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10528194 10310 Cd44 CD44 antigen gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:15585887 10310 Cd44 CD44 antigen gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:15619667 10310 Cd44 CD44 antigen gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:16557236 10310 Cd44 CD44 antigen gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:16816384 10310 Cd44 CD44 antigen gene MP:0002936 joint swelling IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:12437588 10310 Cd44 CD44 antigen gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:10528194 10310 Cd44 CD44 antigen gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:12466136 10310 Cd44 CD44 antigen gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:15919379 10310 Cd44 CD44 antigen gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:19901064 10310 Cd44 CD44 antigen gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:11762953 10310 Cd44 CD44 antigen gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:16816384 10310 Cd44 CD44 antigen gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:16098130 10310 Cd44 CD44 antigen gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:16816384 10310 Cd44 CD44 antigen gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:15596723 10310 Cd44 CD44 antigen gene MP:0003815 hairless IAGP N RGD:5509061 20180712 MGI PMID:22834956 10310 Cd44 CD44 antigen gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:12437588 10310 Cd44 CD44 antigen gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16557236 10310 Cd44 CD44 antigen gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16816384 10310 Cd44 CD44 antigen gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:15901765 10310 Cd44 CD44 antigen gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17923692 10310 Cd44 CD44 antigen gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:23752202 10310 Cd44 CD44 antigen gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12437588 10310 Cd44 CD44 antigen gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10528194 10310 Cd44 CD44 antigen gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:12972514 10310 Cd44 CD44 antigen gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9310473 10310 Cd44 CD44 antigen gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:9637488 10310 Cd44 CD44 antigen gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:15901765 10310 Cd44 CD44 antigen gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:18250474 10310 Cd44 CD44 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23752202 10310 Cd44 CD44 antigen gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11581304 10310 Cd44 CD44 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16098130 10310 Cd44 CD44 antigen gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:10859330 10310 Cd44 CD44 antigen gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:10859330 10310 Cd44 CD44 antigen gene MP:0005546 choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:19339747 10310 Cd44 CD44 antigen gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:15901765 10310 Cd44 CD44 antigen gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:15901765 10310 Cd44 CD44 antigen gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:14551157 10310 Cd44 CD44 antigen gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16816384 10310 Cd44 CD44 antigen gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:16098130 10310 Cd44 CD44 antigen gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9310473 10310 Cd44 CD44 antigen gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16816384 10310 Cd44 CD44 antigen gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:11825873 10310 Cd44 CD44 antigen gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 10310 Cd44 CD44 antigen gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 10310 Cd44 CD44 antigen gene MP:0008162 increased diameter of tibia IAGP N RGD:5509061 20141003 MGI PMID:15619667 10310 Cd44 CD44 antigen gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:15619667 10310 Cd44 CD44 antigen gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:11342603 10310 Cd44 CD44 antigen gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19901064 10310 Cd44 CD44 antigen gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19901064 10310 Cd44 CD44 antigen gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:19901064 10310 Cd44 CD44 antigen gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:11342603 10310 Cd44 CD44 antigen gene MP:0008591 increased circulating interleukin-1 level IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0008599 increased circulating interleukin-2 level IAGP N RGD:5509061 20141003 MGI PMID:11342603 10310 Cd44 CD44 antigen gene MP:0008651 increased interleukin-1 secretion IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:19901064 10310 Cd44 CD44 antigen gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:19901064 10310 Cd44 CD44 antigen gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:19901064 10310 Cd44 CD44 antigen gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:16098130 10310 Cd44 CD44 antigen gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:19901064 10310 Cd44 CD44 antigen gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18483247 10310 Cd44 CD44 antigen gene MP:0008838 decreased transforming growth factor beta level IAGP N RGD:5509061 20141003 MGI PMID:11935029 10310 Cd44 CD44 antigen gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23318432 10310 Cd44 CD44 antigen gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:11342603 10310 Cd44 CD44 antigen gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17923692 10310 Cd44 CD44 antigen gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20160128 MGI PMID:18854186 10310 Cd44 CD44 antigen gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:16557236 10310 Cd44 CD44 antigen gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11342603 10310 Cd44 CD44 antigen gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11935029 10310 Cd44 CD44 antigen gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:19901064 10310 Cd44 CD44 antigen gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:11342603 10310 Cd44 CD44 antigen gene MP:0010677 decreased activation-induced cell death of T cells IAGP N RGD:5509061 20141003 MGI PMID:11342603 10310 Cd44 CD44 antigen gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:17923692 10310 Cd44 CD44 antigen gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17923692 10310 Cd44 CD44 antigen gene MP:0010842 decreased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 10310 Cd44 CD44 antigen gene MP:0010845 decreased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 10310 Cd44 CD44 antigen gene MP:0010848 decreased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 10310 Cd44 CD44 antigen gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:15781582 10310 Cd44 CD44 antigen gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17923692 10310 Cd44 CD44 antigen gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:15126101 10310 Cd44 CD44 antigen gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:15126101 10310 Cd44 CD44 antigen gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:15126101 10310 Cd44 CD44 antigen gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11956084 10310 Cd44 CD44 antigen gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18483247 10310 Cd44 CD44 antigen gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23318432 10310 Cd44 CD44 antigen gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 10310 Cd44 CD44 antigen gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:23318432 10310 Cd44 CD44 antigen gene MP:0014373 increased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:17923692 10310 Cd44 CD44 antigen gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:17923692 10310 Cd44 CD44 antigen gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:17923692 10310 Cd44 CD44 antigen gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:16098130 10313 Cd53 CD53 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20180503 MGI PMID:28487417 10314 Cd59a CD59a antigen gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17429844 10314 Cd59a CD59a antigen gene MP:0000315 hemoglobinuria IAGP N RGD:5509061 20141003 MGI PMID:11435315 10314 Cd59a CD59a antigen gene MP:0000332 hemoglobinemia IAGP N RGD:5509061 20141003 MGI PMID:11435315 10314 Cd59a CD59a antigen gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:14631387 10314 Cd59a CD59a antigen gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11435315 10314 Cd59a CD59a antigen gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17034582 10314 Cd59a CD59a antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17296227 10314 Cd59a CD59a antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:17296227 10314 Cd59a CD59a antigen gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17429844 10314 Cd59a CD59a antigen gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17034582 10314 Cd59a CD59a antigen gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:11986227 10314 Cd59a CD59a antigen gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:15331407 10314 Cd59a CD59a antigen gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:17034582 10314 Cd59a CD59a antigen gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:19246097 10314 Cd59a CD59a antigen gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:11435315 10314 Cd59a CD59a antigen gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:15457473 10314 Cd59a CD59a antigen gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19959238 10314 Cd59a CD59a antigen gene MP:0004041 increased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:15331407 10314 Cd59a CD59a antigen gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15331407 10314 Cd59a CD59a antigen gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:17034582 10314 Cd59a CD59a antigen gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:14631387 10314 Cd59a CD59a antigen gene MP:0004823 increased susceptibility to experimental autoimmune myasthenia gravis IAGP N RGD:5509061 20141003 MGI PMID:17034582 10314 Cd59a CD59a antigen gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17429844 10314 Cd59a CD59a antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17296227 10314 Cd59a CD59a antigen gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:19246097 10314 Cd59a CD59a antigen gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19959238 10314 Cd59a CD59a antigen gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16301611 10314 Cd59a CD59a antigen gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:19246097 10314 Cd59a CD59a antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17296227 10314 Cd59a CD59a antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17429844 10314 Cd59a CD59a antigen gene MP:0005489 vascular smooth muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19959238 10314 Cd59a CD59a antigen gene MP:0005546 choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:17237428 10314 Cd59a CD59a antigen gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17429844 10314 Cd59a CD59a antigen gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17429844 10314 Cd59a CD59a antigen gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:17296227 10314 Cd59a CD59a antigen gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17034582 10314 Cd59a CD59a antigen gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:17034582 10314 Cd59a CD59a antigen gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:17429844 10314 Cd59a CD59a antigen gene MP:0010653 abnormal Wallerian degeneration IAGP N RGD:5509061 20141003 MGI PMID:19246097 10314 Cd59a CD59a antigen gene MP:0020929 decreased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16301611 10314 Cd59a CD59a antigen gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:17429844 10314 Cd59a CD59a antigen gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:11435315 10316 Cd80 CD80 antigen gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12207354 10316 Cd80 CD80 antigen gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9075931 10316 Cd80 CD80 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:9075931 10316 Cd80 CD80 antigen gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:10477557 10316 Cd80 CD80 antigen gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:9075931 10316 Cd80 CD80 antigen gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10453003 10316 Cd80 CD80 antigen gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11169445 10316 Cd80 CD80 antigen gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9075931 10316 Cd80 CD80 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9075931 10316 Cd80 CD80 antigen gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:10453003 10316 Cd80 CD80 antigen gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:10795741 10316 Cd80 CD80 antigen gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:10795741 10316 Cd80 CD80 antigen gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:16886063 10316 Cd80 CD80 antigen gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12207354 10316 Cd80 CD80 antigen gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:10477557 10316 Cd80 CD80 antigen gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12207354 10316 Cd80 CD80 antigen gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10795741 10316 Cd80 CD80 antigen gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:16886063 10316 Cd80 CD80 antigen gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:16886063 10316 Cd80 CD80 antigen gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16886063 10316 Cd80 CD80 antigen gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23793062 10316 Cd80 CD80 antigen gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10725709 10316 Cd80 CD80 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7694362 10316 Cd80 CD80 antigen gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10453003 10316 Cd80 CD80 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10477557 10316 Cd80 CD80 antigen gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10453003 10316 Cd80 CD80 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10795741 10316 Cd80 CD80 antigen gene MP:0005623 abnormal meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:12207354 10316 Cd80 CD80 antigen gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:10725709 10316 Cd80 CD80 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9075931 10316 Cd80 CD80 antigen gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9075931 10316 Cd80 CD80 antigen gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9075931 10316 Cd80 CD80 antigen gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:10477557 10316 Cd80 CD80 antigen gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10477557 10316 Cd80 CD80 antigen gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:12207354 10316 Cd80 CD80 antigen gene MP:0009023 abnormal spinal cord meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:12207354 10317 Cd8a CD8 subunit alpha gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:21964024 10317 Cd8a CD8 subunit alpha gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20180719 MGI PMID:1673361 10317 Cd8a CD8 subunit alpha gene MP:0000921 demyelination IAGP N RGD:5509061 20180719 MGI PMID:9696828 10317 Cd8a CD8 subunit alpha gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20180719 MGI PMID:11114377 10317 Cd8a CD8 subunit alpha gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:15922720 10317 Cd8a CD8 subunit alpha gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:21964024 10317 Cd8a CD8 subunit alpha gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20180719 MGI PMID:8500525 10317 Cd8a CD8 subunit alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:12049715 10317 Cd8a CD8 subunit alpha gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20180719 MGI PMID:8500525 10317 Cd8a CD8 subunit alpha gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20180719 MGI PMID:17082573 10317 Cd8a CD8 subunit alpha gene MP:0002418 increased susceptibility to viral infection IAGP N RGD:5509061 20180719 MGI PMID:7676644 10317 Cd8a CD8 subunit alpha gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20180719 MGI PMID:22036949 10317 Cd8a CD8 subunit alpha gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20180719 MGI PMID:15729333 10317 Cd8a CD8 subunit alpha gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20180719 MGI PMID:17082573 10317 Cd8a CD8 subunit alpha gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IEA N RGD:5509061 20180719 MGI 10317 Cd8a CD8 subunit alpha gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20180719 MGI PMID:8500525 10317 Cd8a CD8 subunit alpha gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20180719 MGI PMID:21964024 10317 Cd8a CD8 subunit alpha gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20180719 MGI PMID:21964024 10317 Cd8a CD8 subunit alpha gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20180719 MGI PMID:17082573 10317 Cd8a CD8 subunit alpha gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20180719 MGI PMID:17873878 10317 Cd8a CD8 subunit alpha gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20180719 MGI PMID:9806635 10317 Cd8a CD8 subunit alpha gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20180719 MGI PMID:1673361 10317 Cd8a CD8 subunit alpha gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20180719 MGI PMID:8500525 10317 Cd8a CD8 subunit alpha gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20180719 MGI PMID:8500525 10317 Cd8a CD8 subunit alpha gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20180719 MGI PMID:14525595 10317 Cd8a CD8 subunit alpha gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20180719 MGI PMID:8500525 10317 Cd8a CD8 subunit alpha gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:17082573 10317 Cd8a CD8 subunit alpha gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20180719 MGI PMID:12049716 10317 Cd8a CD8 subunit alpha gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:17082573 10317 Cd8a CD8 subunit alpha gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20220106 MGI 10317 Cd8a CD8 subunit alpha gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20220106 MGI 10317 Cd8a CD8 subunit alpha gene MP:0008345 abnormal gamma-delta T cell number IAGP N RGD:5509061 20180719 MGI PMID:8500525 10317 Cd8a CD8 subunit alpha gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20180719 MGI PMID:21964024 10317 Cd8a CD8 subunit alpha gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:21964024 10317 Cd8a CD8 subunit alpha gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20180719 MGI PMID:21964024 10317 Cd8a CD8 subunit alpha gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20180719 MGI PMID:21964024 10317 Cd8a CD8 subunit alpha gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20180719 MGI PMID:21964024 10317 Cd8a CD8 subunit alpha gene MP:0011822 increased CD8-positive, alpha-beta memory T cell proliferation IEA N RGD:5509061 20180719 MGI 10317 Cd8a CD8 subunit alpha gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20180719 MGI PMID:8500525 10317 Cd8a CD8 subunit alpha gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180719 MGI PMID:21964024 10317 Cd8a CD8 subunit alpha gene MP:0020916 increased susceptibility to Herpesvirales infection IEA N RGD:5509061 20200430 MGI 10317 Cd8a CD8 subunit alpha gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:9696828 10320 Cdh6 cadherin 6 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:10864459 10320 Cdh6 cadherin 6 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:10864459 10320 Cdh6 cadherin 6 gene MP:0011291 nephron necrosis IAGP N RGD:5509061 20141003 MGI PMID:10864459 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17360455 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8620534 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18591425 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19061836 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23266956 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10911993 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17360455 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:17360455 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:18039844 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:18328429 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:22113502 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:19079609 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:15044451 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:8620534 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18039844 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15899789 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11544531 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20170817 MGI PMID:21804542 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:12368906 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000730 increased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:12368906 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:19398955 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:14724566 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:11891301 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:16620915 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20150910 MGI PMID:17676035 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:20697345 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:22772081 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20160331 MGI PMID:25252692 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:22772081 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21088222 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:21088222 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17360455 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22113502 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17360455 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:22113502 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:11544530 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:14681207 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:15314658 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:15899789 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16585505 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18328429 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23467612 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20150910 MGI PMID:17676035 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160331 MGI PMID:25252692 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11891301 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:16620915 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19339492 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:11891301 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:19339492 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:16620915 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:17987514 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11891301 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:19339492 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:23955081 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:12589020 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12589020 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20211104 MGI PMID:26240281 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001885 mammary gland duct hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15044451 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:17924978 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:19398955 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:9851974 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19339492 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:19339492 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:15314658 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14681207 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15314658 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19465598 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11544530 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11544531 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12368906 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14665695 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14724566 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16015333 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17114584 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17360455 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8620534 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9393858 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9624006 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8620534 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9393858 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:16015333 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:18242513 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16015333 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23565506 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20150910 MGI PMID:17676035 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20171116 MGI PMID:11751631 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20171116 MGI PMID:21118965 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18242513 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141120 MGI PMID:16540681 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20160929 MGI PMID:23858101 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11544530 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14665695 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14724566 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16015333 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17360455 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17676052 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19217431 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8620534 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20160929 MGI PMID:23858101 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20170420 MGI PMID:26987019 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12368906 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15489287 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20160929 MGI PMID:23858101 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20170420 MGI PMID:26987019 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002037 increased fibrohistocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9393858 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11544530 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15314658 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21970857 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23845441 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9393858 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17158963 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8313388 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:14724566 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12670909 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16015333 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17158963 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17438529 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18039844 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18242513 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18328429 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19079609 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19398955 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19805356 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20697345 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22113502 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002083 premature death IAGP N RGD:5509061 20150910 MGI PMID:17676035 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11891301 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:19465598 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:8620534 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20826531 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23845441 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23955081 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20180222 MGI PMID:28652370 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220714 MGI PMID:19339492 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:16037818 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:21970857 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20697345 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15044451 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:8620534 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003099 retina detachment IAGP N RGD:5509061 20141003 MGI PMID:11891301 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003099 retina detachment IAGP N RGD:5509061 20180222 MGI PMID:28652370 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003155 abnormal telomere length IAGP N RGD:5509061 20141003 MGI PMID:17360455 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10911993 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:17360455 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:19339492 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:12589020 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003236 abnormal lens capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:11891301 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:19629168 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20697345 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11551927 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21088222 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003570 increased uterus leiomyoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20220303 MGI PMID:19079609 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:22266795 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14665695 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8620534 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:15314658 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20697345 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11891301 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:17360455 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14724566 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16015333 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:23266956 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20141003 MGI PMID:11551927 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20141003 MGI PMID:21970857 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20211104 MGI PMID:26240281 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20571512 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11551927 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15314658 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:10911993 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11544530 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11544531 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:14724566 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15314658 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17713536 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:19345328 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:9393858 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:14665695 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:9393858 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:17987514 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17713536 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004851 increased testis weight IAGP N RGD:5509061 20180222 MGI PMID:28652370 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19339492 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180222 MGI PMID:28652370 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:11544531 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11544531 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:23955081 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0005195 abnormal posterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16620915 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11891301 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:19629168 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:22113502 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:11551927 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:16620915 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11551927 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14724566 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9393858 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0005623 abnormal meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:17924978 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16620915 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0006148 binocular blindness IAGP N RGD:5509061 20180222 MGI PMID:28652370 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20180222 MGI PMID:28652370 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18039844 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:11551927 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17299132 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20150910 MGI PMID:17676035 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20171116 MGI PMID:11751631 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17924978 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11544531 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11544531 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:8620534 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14724566 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009043 increased pancreas adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22113502 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14681207 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16585505 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17114584 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22611036 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23467612 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:14681207 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22113502 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14681207 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16585505 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19629168 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22113502 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23467612 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19079609 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20639864 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22113502 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009319 increased small lymphocytic lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14724566 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14665695 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11544531 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009459 skeletal muscle hyperplasia IAGP N RGD:5509061 20170420 MGI PMID:26987019 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:15044451 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009515 increased gastrointestinal stromal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14665695 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11551927 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21970857 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009621 primary vitreous hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16037818 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009621 primary vitreous hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19465598 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21970857 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010273 increased classified tumor incidence IAGP N RGD:5509061 20141120 MGI PMID:16540681 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11544530 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12368906 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12902988 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19345328 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19398955 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20048081 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20697345 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20160114 MGI PMID:25705882 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20200402 MGI PMID:27135738 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010276 increased intraocular melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17987514 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:12670909 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:17438529 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:9851974 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17713536 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19345328 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17114584 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:12670909 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:17728759 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010309 increased mesothelioma incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010310 increased Schwannoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010311 increased meningioma incidence IAGP N RGD:5509061 20141003 MGI PMID:17924978 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010311 increased meningioma incidence IAGP N RGD:5509061 20141003 MGI PMID:21242963 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010312 increased oligodendroglioma incidence IAGP N RGD:5509061 20141003 MGI PMID:12670909 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010312 increased oligodendroglioma incidence IAGP N RGD:5509061 20141003 MGI PMID:17438529 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010312 increased oligodendroglioma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805356 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010313 increased osteoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17924978 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15899789 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22772081 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20141120 MGI PMID:16540681 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20160331 MGI PMID:25252692 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20170202 MGI PMID:22983396 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010334 pleural effusion IAGP N RGD:5509061 20141003 MGI PMID:18328429 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20180222 MGI PMID:28652370 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010347 osseous metaplasia IAGP N RGD:5509061 20141003 MGI PMID:17924978 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19217431 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8620534 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9393858 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010367 increased spindle cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20697345 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010367 increased spindle cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21970857 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:11891301 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:16620915 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:19465598 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20180222 MGI PMID:28652370 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010727 increased glioblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19196966 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0010741 abnormal melanocyte proliferation IAGP N RGD:5509061 20160331 MGI PMID:25252692 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10911993 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20211104 MGI PMID:26240281 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20826531 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:15044451 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:8620534 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:9393858 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0011748 intestinal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0012193 increased keratinocyte migration IAGP N RGD:5509061 20141204 MGI PMID:21970857 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11544530 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14665695 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14724566 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16015333 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17360455 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18039844 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18242513 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9393858 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:17360455 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:14681207 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:14724566 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:17114584 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:19196966 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:20697345 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:23467612 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:11891301 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:16620915 10322 Cdkn2a cyclin dependent kinase inhibitor 2A gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:19339492 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:10982846 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18974039 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22715416 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000239 absent common myeloid progenitor cells IAGP N RGD:5509061 20141003 MGI PMID:15589173 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:11672531 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:15589173 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17290224 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:17290224 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22715416 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:16467360 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:19749746 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:19749746 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19749746 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001219 thick epidermis IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:19749746 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:19749746 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001241 absent epidermis stratum corneum IAGP N RGD:5509061 20141003 MGI PMID:19749746 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18974039 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19749746 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:19749746 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001337 dry eyes IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001345 Meibomian gland atrophy IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:10982846 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18974039 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20516642 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18974039 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17290224 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15589173 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22715416 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001603 failure of myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15589173 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:10982846 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11672531 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15130516 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001934 increased litter size IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:16428462 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16428462 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16467360 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:17638888 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9315660 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11672531 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15589173 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15130516 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22715416 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11672531 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15589173 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16428455 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:11683182 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:16428462 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16428462 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002274 abnormal type I pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16467360 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16428462 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16467360 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22715416 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11672531 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:20516642 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002717 abnormal male preputial gland morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20516642 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10982846 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10982846 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0002992 abnormal sebaceous lipid secretion IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22715416 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0003326 liver failure IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:19749746 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0003427 parakeratosis IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:17638888 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20516642 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16467360 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17638888 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:20516642 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:11683182 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:16428462 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:16467360 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22715416 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:15589173 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18974039 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005252 abnormal Meibomian gland morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17290224 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:11672531 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20516642 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17290224 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20516642 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:10982846 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0008991 abnormal bile canaliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10982846 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17290224 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0009560 absent epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:19749746 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19749746 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:16467360 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17638888 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:17290224 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010682 abnormal hair follicle infundibulum morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010688 hair follicle outer root sheath hyperplasia IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:11683182 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010812 absent type II pneumocytes IAGP N RGD:5509061 20141003 MGI PMID:16428462 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010814 absent alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:16428462 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010817 absent type I pneumocytes IAGP N RGD:5509061 20141003 MGI PMID:16428462 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010817 absent type I pneumocytes IAGP N RGD:5509061 20141003 MGI PMID:16467360 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:16467360 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0010903 abnormal pulmonary alveolus wall morphology IAGP N RGD:5509061 20141003 MGI PMID:11683182 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18394553 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16467360 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19749746 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16428462 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8798745 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:10982846 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0013375 abnormal sebocyte morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0013376 abnormal sebocyte differentiation IAGP N RGD:5509061 20150813 MGI PMID:20352127 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0013723 increased circulating tyrosine level IAGP N RGD:5509061 20150409 MGI PMID:7652557 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0014473 increased pulmonary alveolus wall thickness IAGP N RGD:5509061 20240704 MGI PMID:16428462 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:17290224 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:15319454 10325 Cebpa CCAAT/enhancer binding protein alpha gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:17290224 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:10747954 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:9727068 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:9916132 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20047998 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:9637691 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:9637692 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:9637691 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:9637692 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:9303532 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:9303532 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:19749746 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:19749746 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19749746 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001219 thick epidermis IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:19749746 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:19749746 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001241 absent epidermis stratum corneum IAGP N RGD:5509061 20141003 MGI PMID:19749746 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20171228 MGI PMID:15762841 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19749746 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:19749746 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001337 dry eyes IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001345 Meibomian gland atrophy IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20171228 MGI PMID:15762841 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001553 abnormal circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:9916132 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19955657 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:9916132 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20171228 MGI PMID:15762841 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:9405372 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:7530603 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:9637691 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9303532 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9405372 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9637692 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:11756662 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10747954 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9727068 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9916132 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19955657 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10747954 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9916132 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20047998 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002343 abnormal lymph node cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002346 abnormal lymph node secondary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002347 abnormal lymph node T cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002348 abnormal lymph node medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002377 abnormal mucosa-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20180906 MGI PMID:28476751 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17911624 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:7530603 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17911624 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:7530603 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:17911624 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9916132 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:10747954 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:9916132 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002715 decreased glycogen catabolism rate IAGP N RGD:5509061 20141003 MGI PMID:9916132 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002717 abnormal male preputial gland morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10747954 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19955657 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002742 enlarged submandibular lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:10747954 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9405372 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0002992 abnormal sebaceous lipid secretion IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19955657 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19955657 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0003199 calcified muscle IAGP N RGD:5509061 20141003 MGI PMID:19805133 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0003356 impaired luteinization IAGP N RGD:5509061 20141003 MGI PMID:9303532 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0003357 impaired granulosa cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9303532 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:9727068 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:9916132 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:19749746 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0003427 parakeratosis IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:11756662 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20170202 MGI PMID:24885110 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11756662 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16205634 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:19805133 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20170202 MGI PMID:24885110 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0004817 abnormal skeletal muscle mass IAGP N RGD:5509061 20170202 MGI PMID:24885110 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:20047998 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:20047998 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9405372 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005252 abnormal Meibomian gland morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20170202 MGI PMID:24885110 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20171228 MGI PMID:15762841 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:9916132 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:10747954 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:17911624 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:20047998 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:9727068 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19955657 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20171228 MGI PMID:15762841 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:9916132 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:10747954 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:10747954 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008472 abnormal spleen secondary B follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20180906 MGI PMID:28476751 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20180906 MGI PMID:28476751 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20047998 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20180906 MGI PMID:28476751 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008618 decreased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:17724128 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17911624 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:23177475 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008838 decreased transforming growth factor beta level IAGP N RGD:5509061 20180906 MGI PMID:28476751 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19805133 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:9531536 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:9303532 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009112 abnormal pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:19955657 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:19955657 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9405372 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009134 abnormal brown fat lipid droplet number IAGP N RGD:5509061 20141003 MGI PMID:9405372 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10747954 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:9405372 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20171228 MGI PMID:15762841 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009307 decreased uterine fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:9916132 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:20047998 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:19805133 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19805133 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009488 abnormal pancreatic islet cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19955657 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:9637692 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009560 absent epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:19749746 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11756662 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16205634 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19749746 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009623 enlarged inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009631 enlarged axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20180906 MGI PMID:28476751 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0010172 abnormal mammary gland epithelium physiology IAGP N RGD:5509061 20150611 MGI PMID:9637692 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0010682 abnormal hair follicle infundibulum morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0010688 hair follicle outer root sheath hyperplasia IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:20047998 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20171228 MGI PMID:15762841 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7530603 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9405372 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19749746 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9405372 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9405372 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7530603 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9405372 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9303532 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011224 abnormal lymph node medullary cord morphology IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:7744000 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011579 decreased lipoprotein lipase activity IAGP N RGD:5509061 20171228 MGI PMID:15762841 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20171228 MGI PMID:15762841 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:9405372 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:19805133 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0013375 abnormal sebocyte morphology IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0013376 abnormal sebocyte differentiation IAGP N RGD:5509061 20150813 MGI PMID:20352127 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0013661 abnormal myeloid cell number IAGP N RGD:5509061 20180906 MGI PMID:28476751 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:19440205 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:9303532 10326 Cebpb CCAAT/enhancer binding protein beta gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:10747954 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:12626772 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:9724803 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:9405372 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23177475 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:23177475 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9405372 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9405372 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:23177475 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:9405372 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:23177475 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0008822 decreased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:16873376 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9405372 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0009134 abnormal brown fat lipid droplet number IAGP N RGD:5509061 20141003 MGI PMID:9405372 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:9405372 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12626772 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16873376 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0009810 increased urine uric acid level IAGP N RGD:5509061 20141003 MGI PMID:16873376 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0010173 increased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12626772 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9405372 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9405372 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:9405372 10327 Cebpd CCAAT/enhancer binding protein delta gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:16873376 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0001867 rhinitis IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0002415 abnormal neutrophil differentiation IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0002443 abnormal eosinophil differentiation IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0005190 osteomyelitis IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:9371821 10328 Cebpe CCAAT/enhancer binding protein epsilon gene MP:0031053 pleuritis IAGP N RGD:5509061 20200618 MGI PMID:9371821 10329 Cebpg CCAAT/enhancer binding protein gamma gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:10587348 10329 Cebpg CCAAT/enhancer binding protein gamma gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:10587348 10329 Cebpg CCAAT/enhancer binding protein gamma gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10587348 10329 Cebpg CCAAT/enhancer binding protein gamma gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10587348 10330 Cel carboxyl ester lipase gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:17604277 10330 Cel carboxyl ester lipase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17604277 10330 Cel carboxyl ester lipase gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17604277 10330 Cel carboxyl ester lipase gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17604277 10330 Cel carboxyl ester lipase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17604277 10330 Cel carboxyl ester lipase gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17604277 10330 Cel carboxyl ester lipase gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:10194330 10330 Cel carboxyl ester lipase gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:17604277 10330 Cel carboxyl ester lipase gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:8636157 10330 Cel carboxyl ester lipase gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17604277 10330 Cel carboxyl ester lipase gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17604277 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20160519 MGI PMID:15246977 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:17519339 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:7560099 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9399953 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:15921521 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:7482032 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20160519 MGI PMID:8589719 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:7527588 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:1382232 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20160519 MGI PMID:8589719 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001135 abnormal uterine cervix morphology IAGP N RGD:5509061 20141003 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:7540910 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:1382232 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001258 decreased body length IAGP N RGD:5509061 20180830 MGI PMID:29924856 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15921521 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7556083 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7560099 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180830 MGI PMID:29924856 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001263 weight loss IAGP N RGD:5509061 20160519 MGI PMID:8589719 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7482032 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7560099 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001265 decreased body size IAGP N RGD:5509061 20160519 MGI PMID:8589719 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001265 decreased body size IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001346 abnormal lacrimal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001511 disheveled coat IAGP N RGD:5509061 20220505 MGI PMID:35392567 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:11823443 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:7482032 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:7560099 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7556083 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9399953 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160519 MGI PMID:15246977 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160519 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160519 MGI PMID:18802965 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160519 MGI PMID:8589719 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7560099 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:7560099 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:15921521 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:10570187 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:15246977 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:7540910 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:9399953 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17519339 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:7482032 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17519339 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:7482032 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0001947 abnormal mucociliary clearance IAGP N RGD:5509061 20151224 MGI PMID:22937152 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:1355249 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18802965 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7482032 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002083 premature death IAGP N RGD:5509061 20160519 MGI PMID:7545494 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002083 premature death IAGP N RGD:5509061 20180830 MGI PMID:29924856 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002083 premature death IAGP N RGD:5509061 20220505 MGI PMID:35392567 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11823443 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002163 abnormal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002163 abnormal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18802965 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7560099 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002238 abnormal nasal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002240 abnormal paranasal sinus morphology IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:9399953 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:9399953 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002309 abnormal vital capacity IAGP N RGD:5509061 20141003 MGI PMID:9399953 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20151224 MGI PMID:22937152 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:7540910 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17519339 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:7560099 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:1382232 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003251 gallbladder inflammation IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:1355249 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:15246977 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:16571105 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:7482032 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:7560099 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20160519 MGI PMID:18802965 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20160519 MGI PMID:7545494 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20160519 MGI PMID:8589719 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20180830 MGI PMID:29924856 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20220505 MGI PMID:35392567 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:7560099 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20160519 MGI PMID:7545494 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003340 acute pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003426 pulmonary interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9399953 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11823443 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18802965 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22711878 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7527588 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7556083 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20220505 MGI PMID:35392567 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20141003 MGI PMID:17519339 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20141003 MGI PMID:7560099 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:17506901 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:10570187 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22711878 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20160519 MGI PMID:7545494 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:7556083 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20160519 MGI PMID:7545494 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0005084 abnormal gallbladder morphology IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0005085 abnormal gallbladder physiology IAGP N RGD:5509061 20141003 MGI PMID:7556083 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20160519 MGI PMID:15246977 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20180830 MGI PMID:29924856 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17947234 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20220505 MGI PMID:35392567 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0009081 thin uterus IAGP N RGD:5509061 20141003 MGI PMID:18325992 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0009150 pancreatic acinar cell atrophy IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0009161 pancreatic acinar cell zymogen granule accumulation IAGP N RGD:5509061 20141003 MGI PMID:10570187 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0009342 enlarged gallbladder IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0009342 enlarged gallbladder IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0009343 dilated gallbladder IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0009477 small cecum IAGP N RGD:5509061 20141003 MGI PMID:1355249 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0009478 coiled cecum IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0009478 coiled cecum IAGP N RGD:5509061 20141003 MGI PMID:7527588 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0009484 ileum hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10570187 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20160519 MGI PMID:15246977 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20160519 MGI PMID:11102538 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20160519 MGI PMID:7545494 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0010156 abnormal small intestinal crypt cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22711878 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0010156 abnormal small intestinal crypt cell physiology IAGP N RGD:5509061 20160519 MGI PMID:8589719 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16571105 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0010858 pulmonary epithelial necrosis IAGP N RGD:5509061 20151224 MGI PMID:22937152 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0010861 increased respiratory mucosa goblet cell number IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0010861 increased respiratory mucosa goblet cell number IAGP N RGD:5509061 20141003 MGI PMID:7540910 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:9399953 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160519 MGI PMID:8589719 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1355249 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7527588 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7560099 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7949729 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9399953 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20151224 MGI PMID:22937152 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160519 MGI PMID:11102538 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160519 MGI PMID:18802965 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160519 MGI PMID:7545494 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160519 MGI PMID:8589719 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20220505 MGI PMID:35392567 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20160519 MGI PMID:8589719 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0012518 abnormal Brunner's gland morphology IAGP N RGD:5509061 20141003 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0012519 dilated Brunner's gland IAGP N RGD:5509061 20141003 MGI PMID:7560099 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0013455 lacrimal gland atrophy IAGP N RGD:5509061 20150205 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0013494 abnormal trachea gland morphology IAGP N RGD:5509061 20150212 MGI PMID:1380723 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0013792 abnormal small intestine goblet cell morphology IAGP N RGD:5509061 20160519 MGI PMID:8589719 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:7527588 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20160519 MGI PMID:8589719 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0013797 abnormal ileal goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:16571105 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014028 decreased respiratory epithelial chloride transmembrane transport IAGP N RGD:5509061 20160519 MGI PMID:15246977 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014028 decreased respiratory epithelial chloride transmembrane transport IAGP N RGD:5509061 20160519 MGI PMID:18802965 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014028 decreased respiratory epithelial chloride transmembrane transport IAGP N RGD:5509061 20160519 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014028 decreased respiratory epithelial chloride transmembrane transport IAGP N RGD:5509061 20160519 MGI PMID:7545494 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014028 decreased respiratory epithelial chloride transmembrane transport IAGP N RGD:5509061 20160519 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014028 decreased respiratory epithelial chloride transmembrane transport IAGP N RGD:5509061 20160526 MGI PMID:1382232 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014028 decreased respiratory epithelial chloride transmembrane transport IAGP N RGD:5509061 20160526 MGI PMID:7556083 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014028 decreased respiratory epithelial chloride transmembrane transport IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014028 decreased respiratory epithelial chloride transmembrane transport IAGP N RGD:5509061 20160526 MGI PMID:9399953 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014033 abnormal submucosal gland morphology IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014036 meconium ileus IAGP N RGD:5509061 20160519 MGI PMID:7545494 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014036 meconium ileus IAGP N RGD:5509061 20160519 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014036 meconium ileus IAGP N RGD:5509061 20160519 MGI PMID:8589719 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014036 meconium ileus IAGP N RGD:5509061 20160526 MGI PMID:1355249 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014036 meconium ileus IAGP N RGD:5509061 20160526 MGI PMID:7949729 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014079 decreased small intestinal villus number IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014182 decreased respiratory epithelial sodium ion transmembrane transport IAGP N RGD:5509061 20160519 MGI PMID:15246977 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014182 decreased respiratory epithelial sodium ion transmembrane transport IAGP N RGD:5509061 20160519 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014182 decreased respiratory epithelial sodium ion transmembrane transport IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014183 increased respiratory epithelial sodium ion transmembrane transport IAGP N RGD:5509061 20160519 MGI PMID:8589719 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014206 decreased intestinal epithelial sodium ion transmembrane transport IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014208 decreased intestinal epithelial chloride transmembrane transport IAGP N RGD:5509061 20160526 MGI PMID:1382232 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014208 decreased intestinal epithelial chloride transmembrane transport IAGP N RGD:5509061 20160526 MGI PMID:18802965 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014208 decreased intestinal epithelial chloride transmembrane transport IAGP N RGD:5509061 20160526 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014208 decreased intestinal epithelial chloride transmembrane transport IAGP N RGD:5509061 20160526 MGI PMID:7527588 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014208 decreased intestinal epithelial chloride transmembrane transport IAGP N RGD:5509061 20160526 MGI PMID:7556083 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014226 abnormal alveolar macrophage physiology IAGP N RGD:5509061 20160526 MGI PMID:16921366 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014230 dilated crypt of Lieberkuhn IAGP N RGD:5509061 20160526 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014230 dilated crypt of Lieberkuhn IAGP N RGD:5509061 20160526 MGI PMID:7527588 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014230 dilated crypt of Lieberkuhn IAGP N RGD:5509061 20160526 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014230 dilated crypt of Lieberkuhn IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014230 dilated crypt of Lieberkuhn IAGP N RGD:5509061 20220505 MGI PMID:35392567 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014231 intestinal mucus accumulation IAGP N RGD:5509061 20160526 MGI PMID:18802965 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014231 intestinal mucus accumulation IAGP N RGD:5509061 20160526 MGI PMID:7505691 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014231 intestinal mucus accumulation IAGP N RGD:5509061 20160526 MGI PMID:7685652 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014232 dilated pancreatic acinus IAGP N RGD:5509061 20160526 MGI PMID:10570187 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0014233 bile duct epithelium hyperplasia IAGP N RGD:5509061 20160526 MGI PMID:8605891 10331 Cftr cystic fibrosis transmembrane conductance regulator gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220303 MGI PMID:18325992 10339 Chga chromogranin A gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:16007257 10339 Chga chromogranin A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16007257 10339 Chga chromogranin A gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20141003 MGI PMID:16007257 10339 Chga chromogranin A gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16007257 10339 Chga chromogranin A gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:16007257 10339 Chga chromogranin A gene MP:0002909 abnormal adrenal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:16007257 10339 Chga chromogranin A gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:16007257 10339 Chga chromogranin A gene MP:0005662 increased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:16007257 10339 Chga chromogranin A gene MP:0005665 increased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:16007257 10339 Chga chromogranin A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16007257 10339 Chga chromogranin A gene MP:0011478 abnormal urine catecholamine level IAGP N RGD:5509061 20141003 MGI PMID:16556729 10339 Chga chromogranin A gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:16007257 10339 Chga chromogranin A gene MP:0030762 decreased adrenaline level IAGP N RGD:5509061 20180927 MGI PMID:16007257 10340 Chgb chromogranin B gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20141003 MGI PMID:20089903 10340 Chgb chromogranin B gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20126668 10340 Chgb chromogranin B gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20126668 10340 Chgb chromogranin B gene MP:0008504 abnormal adrenal chromaffin cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20089903 10340 Chgb chromogranin B gene MP:0010147 abnormal endocrine pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:20126668 10340 Chgb chromogranin B gene MP:0030762 decreased adrenaline level IAGP N RGD:5509061 20180927 MGI PMID:20089903 10343 Chm CHM Rab escort protein gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:16410831 10343 Chm CHM Rab escort protein gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:9175730 10343 Chm CHM Rab escort protein gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:15242790 10343 Chm CHM Rab escort protein gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:15242790 10343 Chm CHM Rab escort protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16410831 10343 Chm CHM Rab escort protein gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:15242790 10343 Chm CHM Rab escort protein gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:15242790 10343 Chm CHM Rab escort protein gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:16410831 10343 Chm CHM Rab escort protein gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16410831 10343 Chm CHM Rab escort protein gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15242790 10343 Chm CHM Rab escort protein gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16410831 10343 Chm CHM Rab escort protein gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15242790 10343 Chm CHM Rab escort protein gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15242790 10343 Chm CHM Rab escort protein gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:15242790 10343 Chm CHM Rab escort protein gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15242790 10343 Chm CHM Rab escort protein gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16410831 10343 Chm CHM Rab escort protein gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16410831 10343 Chm CHM Rab escort protein gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15242790 10343 Chm CHM Rab escort protein gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:16410831 10343 Chm CHM Rab escort protein gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:16410831 10343 Chm CHM Rab escort protein gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:16410831 10343 Chm CHM Rab escort protein gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:15242790 10343 Chm CHM Rab escort protein gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9175730 10343 Chm CHM Rab escort protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15242790 10343 Chm CHM Rab escort protein gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15242790 10343 Chm CHM Rab escort protein gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20141003 MGI PMID:15242790 10343 Chm CHM Rab escort protein gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:15242790 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11961069 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10468635 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:12729838 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20147565 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:18382674 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:10688600 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:20147565 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15919709 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0002822 catalepsy IAGP N RGD:5509061 20141003 MGI PMID:20147565 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:15919709 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:20147565 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:16110248 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0005085 abnormal gallbladder physiology IAGP N RGD:5509061 20141003 MGI PMID:11961069 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12729838 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20147565 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20147565 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:20147565 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:20147565 10353 Chrm4 cholinergic receptor, muscarinic 4 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:10468635 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10964949 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:11226318 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:10964949 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:11226318 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:10964949 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15963492 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:10235262 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:17146052 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10235262 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15963492 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15963492 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:12623222 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:10964949 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:11226318 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:12623222 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17146052 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:10964949 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:17146052 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:21795541 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:17146052 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:12623222 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:17146052 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:20061993 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0008035 behavioral arrest IAGP N RGD:5509061 20141003 MGI PMID:17146052 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0009475 abnormal nicotine-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:10235262 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:20061993 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:21795541 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0009713 enhanced conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:15528443 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:10964949 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:17881519 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:20061993 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:11226318 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20141003 MGI PMID:11226318 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20141003 MGI PMID:15528443 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20141003 MGI PMID:21795541 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0009756 impaired behavioral response to nicotine IAGP N RGD:5509061 20141003 MGI PMID:17881519 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0009756 impaired behavioral response to nicotine IAGP N RGD:5509061 20141003 MGI PMID:21795541 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20141003 MGI PMID:21795541 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11226318 10355 Chrna4 cholinergic receptor, nicotinic, alpha polypeptide 4 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:11226318 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0000088 short mandible IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18083057 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10800961 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141120 MGI PMID:24983521 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10800961 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20141003 MGI PMID:11834293 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0001054 failure of neuromuscular synapse presynaptic differentiation IAGP N RGD:5509061 20141003 MGI PMID:20498043 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10454356 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15541879 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15541879 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10800961 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:10800961 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10454356 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0001505 hunched posture IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0001577 anemia IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15963492 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:9364063 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15364017 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15364017 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10800961 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9364063 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150409 MGI PMID:24879866 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18083057 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15963492 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15944242 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:20128845 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0003052 omphalocele IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0003054 spina bifida IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10800961 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141120 MGI PMID:24983521 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:15541879 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:15541879 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141120 MGI PMID:24983521 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141120 MGI PMID:24983521 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141120 MGI PMID:24983521 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18083057 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0006408 dorsal root ganglion hypoplasia IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141120 MGI PMID:20713028 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:12508119 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:12508119 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:15364017 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0009475 abnormal nicotine-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:10800961 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0009475 abnormal nicotine-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:9364063 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0009516 enlarged salivary gland IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141120 MGI PMID:24983521 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10800961 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0011114 abnormal airway basal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19808646 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0011115 airway basal cell hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19808646 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:18083057 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0011987 abnormal GABAergic neuron physiology IAGP N RGD:5509061 20141120 MGI PMID:24983521 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0012174 flat head IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0012709 delayed caudal neuropore closure IAGP N RGD:5509061 20151001 MGI PMID:22473653 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:16923147 10357 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7 gene MP:0030091 macrodontia IAGP N RGD:5509061 20171005 MGI PMID:22473653 10358 Chrnb1 cholinergic receptor nicotinic beta 1 subunit gene MP:0000111 cleft palate IEA N RGD:5509061 20240523 MGI 10358 Chrnb1 cholinergic receptor nicotinic beta 1 subunit gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:17959719 10358 Chrnb1 cholinergic receptor nicotinic beta 1 subunit gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 10358 Chrnb1 cholinergic receptor nicotinic beta 1 subunit gene MP:0001406 abnormal gait IEA N RGD:5509061 20240523 MGI 10358 Chrnb1 cholinergic receptor nicotinic beta 1 subunit gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20240523 MGI 10358 Chrnb1 cholinergic receptor nicotinic beta 1 subunit gene MP:0001785 edema IEA N RGD:5509061 20240523 MGI 10358 Chrnb1 cholinergic receptor nicotinic beta 1 subunit gene MP:0001914 hemorrhage IEA N RGD:5509061 20240523 MGI 10358 Chrnb1 cholinergic receptor nicotinic beta 1 subunit gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20240523 MGI 10358 Chrnb1 cholinergic receptor nicotinic beta 1 subunit gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:17959719 10358 Chrnb1 cholinergic receptor nicotinic beta 1 subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 10358 Chrnb1 cholinergic receptor nicotinic beta 1 subunit gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 10364 Ckb creatine kinase, brain gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:15639173 10364 Ckb creatine kinase, brain gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15639173 10364 Ckb creatine kinase, brain gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:12059977 10364 Ckb creatine kinase, brain gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 10364 Ckb creatine kinase, brain gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:15639173 10364 Ckb creatine kinase, brain gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12059977 10364 Ckb creatine kinase, brain gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15639173 10364 Ckb creatine kinase, brain gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15639173 10364 Ckb creatine kinase, brain gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15639173 10364 Ckb creatine kinase, brain gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20181227 MGI 10364 Ckb creatine kinase, brain gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:15639173 10364 Ckb creatine kinase, brain gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 10364 Ckb creatine kinase, brain gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12059977 10364 Ckb creatine kinase, brain gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15639173 10364 Ckb creatine kinase, brain gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:12059977 10364 Ckb creatine kinase, brain gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 10364 Ckb creatine kinase, brain gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 10364 Ckb creatine kinase, brain gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 10364 Ckb creatine kinase, brain gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 10364 Ckb creatine kinase, brain gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:15639173 10364 Ckb creatine kinase, brain gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20211021 MGI 10364 Ckb creatine kinase, brain gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 10364 Ckb creatine kinase, brain gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 10364 Ckb creatine kinase, brain gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 10364 Ckb creatine kinase, brain gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 10367 Clps colipase, pancreatic gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19622781 10367 Clps colipase, pancreatic gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 10367 Clps colipase, pancreatic gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 10367 Clps colipase, pancreatic gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:11751900 10367 Clps colipase, pancreatic gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 10367 Clps colipase, pancreatic gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11751900 10367 Clps colipase, pancreatic gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11751900 10367 Clps colipase, pancreatic gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:11751900 10367 Clps colipase, pancreatic gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:11751900 10367 Clps colipase, pancreatic gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11751900 10367 Clps colipase, pancreatic gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19622781 10367 Clps colipase, pancreatic gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11751900 10367 Clps colipase, pancreatic gene MP:0002791 steatorrhea IAGP N RGD:5509061 20141003 MGI PMID:11751900 10367 Clps colipase, pancreatic gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:11751900 10367 Clps colipase, pancreatic gene MP:0003849 greasy coat IAGP N RGD:5509061 20141003 MGI PMID:11751900 10367 Clps colipase, pancreatic gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11751900 10367 Clps colipase, pancreatic gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19622781 10367 Clps colipase, pancreatic gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:11751900 10367 Clps colipase, pancreatic gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11751900 10367 Clps colipase, pancreatic gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 10367 Clps colipase, pancreatic gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10367 Clps colipase, pancreatic gene MP:0030531 abnormal facial skin morphology IAGP N RGD:5509061 20180118 MGI PMID:11751900 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:16421286 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:16611851 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:16611851 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:16611851 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:16421286 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16611851 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20160421 MGI 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20141003 MGI PMID:16421286 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20141003 MGI PMID:16611851 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:16421286 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16421286 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:16421286 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:16611851 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20150122 MGI PMID:22917771 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20150122 MGI PMID:24641901 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20150122 MGI PMID:24641901 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:16611851 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16611851 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0011464 bilirubinuria IAGP N RGD:5509061 20141003 MGI PMID:16611851 10368 Abcc2 ATP-binding cassette, sub-family member 2 gene MP:0011464 bilirubinuria IAGP N RGD:5509061 20150122 MGI PMID:22917771 10370 Cnr1 cannabinoid receptor 1 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15908955 10370 Cnr1 cannabinoid receptor 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17525344 10370 Cnr1 cannabinoid receptor 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20150108 MGI PMID:24719095 10370 Cnr1 cannabinoid receptor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14770190 10370 Cnr1 cannabinoid receptor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21406230 10370 Cnr1 cannabinoid receptor 1 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:11823890 10370 Cnr1 cannabinoid receptor 1 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:15078564 10370 Cnr1 cannabinoid receptor 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:11823890 10370 Cnr1 cannabinoid receptor 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12405999 10370 Cnr1 cannabinoid receptor 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15078564 10370 Cnr1 cannabinoid receptor 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23785142 10370 Cnr1 cannabinoid receptor 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:9888857 10370 Cnr1 cannabinoid receptor 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10318961 10370 Cnr1 cannabinoid receptor 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10318962 10370 Cnr1 cannabinoid receptor 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21406230 10370 Cnr1 cannabinoid receptor 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:9888857 10370 Cnr1 cannabinoid receptor 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:12152079 10370 Cnr1 cannabinoid receptor 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23785142 10370 Cnr1 cannabinoid receptor 1 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:18256258 10370 Cnr1 cannabinoid receptor 1 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:16571781 10370 Cnr1 cannabinoid receptor 1 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:21406230 10370 Cnr1 cannabinoid receptor 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:18833324 10370 Cnr1 cannabinoid receptor 1 gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:15078564 10370 Cnr1 cannabinoid receptor 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 10370 Cnr1 cannabinoid receptor 1 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:12060781 10370 Cnr1 cannabinoid receptor 1 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:12152079 10370 Cnr1 cannabinoid receptor 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:10318961 10370 Cnr1 cannabinoid receptor 1 gene MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20150108 MGI PMID:24719095 10370 Cnr1 cannabinoid receptor 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 10370 Cnr1 cannabinoid receptor 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:12152079 10370 Cnr1 cannabinoid receptor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10318961 10370 Cnr1 cannabinoid receptor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21406230 10370 Cnr1 cannabinoid receptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23785142 10370 Cnr1 cannabinoid receptor 1 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:15078564 10370 Cnr1 cannabinoid receptor 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14770190 10370 Cnr1 cannabinoid receptor 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:10318962 10370 Cnr1 cannabinoid receptor 1 gene MP:0002798 abnormal active avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:11823890 10370 Cnr1 cannabinoid receptor 1 gene MP:0002822 catalepsy IAGP N RGD:5509061 20141003 MGI PMID:10318961 10370 Cnr1 cannabinoid receptor 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:14770190 10370 Cnr1 cannabinoid receptor 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:14526074 10370 Cnr1 cannabinoid receptor 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:16908411 10370 Cnr1 cannabinoid receptor 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:23785142 10370 Cnr1 cannabinoid receptor 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:12060781 10370 Cnr1 cannabinoid receptor 1 gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:23785142 10370 Cnr1 cannabinoid receptor 1 gene MP:0002918 abnormal paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:12152079 10370 Cnr1 cannabinoid receptor 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:11734603 10370 Cnr1 cannabinoid receptor 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16908411 10370 Cnr1 cannabinoid receptor 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10619457 10370 Cnr1 cannabinoid receptor 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12152079 10370 Cnr1 cannabinoid receptor 1 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:10318961 10370 Cnr1 cannabinoid receptor 1 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:12427832 10370 Cnr1 cannabinoid receptor 1 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:11823890 10370 Cnr1 cannabinoid receptor 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:19607846 10370 Cnr1 cannabinoid receptor 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:9888857 10370 Cnr1 cannabinoid receptor 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:21050275 10370 Cnr1 cannabinoid receptor 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:20080779 10370 Cnr1 cannabinoid receptor 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:18833324 10370 Cnr1 cannabinoid receptor 1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:21050275 10370 Cnr1 cannabinoid receptor 1 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:21406230 10370 Cnr1 cannabinoid receptor 1 gene MP:0004209 abnormal sweet taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20080779 10370 Cnr1 cannabinoid receptor 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20150108 MGI PMID:24719095 10370 Cnr1 cannabinoid receptor 1 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20150108 MGI PMID:24719095 10370 Cnr1 cannabinoid receptor 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 10370 Cnr1 cannabinoid receptor 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:15266010 10370 Cnr1 cannabinoid receptor 1 gene MP:0005131 increased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:18833324 10370 Cnr1 cannabinoid receptor 1 gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:18833324 10370 Cnr1 cannabinoid receptor 1 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:18833324 10370 Cnr1 cannabinoid receptor 1 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:14770190 10370 Cnr1 cannabinoid receptor 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18719666 10370 Cnr1 cannabinoid receptor 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:14770190 10370 Cnr1 cannabinoid receptor 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:14770190 10370 Cnr1 cannabinoid receptor 1 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:12427832 10370 Cnr1 cannabinoid receptor 1 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:12427832 10370 Cnr1 cannabinoid receptor 1 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:14526074 10370 Cnr1 cannabinoid receptor 1 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:10318961 10370 Cnr1 cannabinoid receptor 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:10318961 10370 Cnr1 cannabinoid receptor 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21406230 10370 Cnr1 cannabinoid receptor 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20150108 MGI PMID:24719095 10370 Cnr1 cannabinoid receptor 1 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:21050275 10370 Cnr1 cannabinoid receptor 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23785142 10370 Cnr1 cannabinoid receptor 1 gene MP:0009710 anhedonia IAGP N RGD:5509061 20141003 MGI PMID:11823890 10370 Cnr1 cannabinoid receptor 1 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:9888857 10370 Cnr1 cannabinoid receptor 1 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12917492 10370 Cnr1 cannabinoid receptor 1 gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:10318961 10370 Cnr1 cannabinoid receptor 1 gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:9888857 10370 Cnr1 cannabinoid receptor 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20141003 MGI PMID:9888857 10370 Cnr1 cannabinoid receptor 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12427832 10370 Cnr1 cannabinoid receptor 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:14526074 10370 Cnr1 cannabinoid receptor 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23785142 10370 Cnr1 cannabinoid receptor 1 gene MP:0009775 increased behavioral withdrawal response IAGP N RGD:5509061 20150108 MGI PMID:24719095 10370 Cnr1 cannabinoid receptor 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:14770190 10370 Cnr1 cannabinoid receptor 1 gene MP:0010119 abnormal bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15908955 10370 Cnr1 cannabinoid receptor 1 gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20141003 MGI PMID:19607846 10370 Cnr1 cannabinoid receptor 1 gene MP:0011082 abnormal gastrointestinal motility IAGP N RGD:5509061 20141003 MGI PMID:22836266 10370 Cnr1 cannabinoid receptor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10318961 10370 Cnr1 cannabinoid receptor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 10370 Cnr1 cannabinoid receptor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 10370 Cnr1 cannabinoid receptor 1 gene MP:0012009 early parturition IAGP N RGD:5509061 20141003 MGI PMID:18833324 10370 Cnr1 cannabinoid receptor 1 gene MP:0014440 increased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:12060781 10370 Cnr1 cannabinoid receptor 1 gene MP:0014440 increased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:14770190 10370 Cnr1 cannabinoid receptor 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 10370 Cnr1 cannabinoid receptor 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:9888857 10370 Cnr1 cannabinoid receptor 1 gene MP:0031426 increased sperm motility IAGP N RGD:5509061 20220714 MGI PMID:17395184 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11668593 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11668593 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11668593 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:11668593 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11668593 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11668593 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20181227 MGI 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:10581026 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0003393 decreased cardiac output IEA N RGD:5509061 20210128 MGI 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220519 MGI 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0004591 enlarged tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:10581026 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:10581026 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0004749 nonsyndromic hearing loss IAGP N RGD:5509061 20141003 MGI PMID:10581026 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:10581026 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:11668593 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:11668593 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11668593 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220519 MGI 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0011896 increased circulating unsaturated transferrin level IEA N RGD:5509061 20211021 MGI 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:10581026 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11668593 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0012546 triangular face IAGP N RGD:5509061 20141003 MGI PMID:11668593 10371 Col11a2 collagen, type XI, alpha 2 gene MP:0030049 prominent forehead IAGP N RGD:5509061 20170921 MGI PMID:11668593 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:24334604 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:24334604 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:24334604 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:24334604 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:24334604 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20141003 MGI PMID:24334604 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:24334604 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0010225 abnormal quadriceps morphology IAGP N RGD:5509061 20141003 MGI PMID:24334604 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:24334604 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160616 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:21670218 10372 Col12a1 collagen, type XII, alpha 1 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20190704 MGI PMID:21670218 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:7276808 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:7276808 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20171026 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21917142 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:7276808 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:7276808 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:9832566 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7276808 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8989518 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9832566 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:7276808 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000445 short snout IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000445 short snout IAGP N RGD:5509061 20180503 MGI PMID:26545783 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20171026 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:7276808 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:8989518 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20180503 MGI PMID:26545783 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000550 abnormal forelimb morphology IEA N RGD:5509061 20111116 MGI 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20111116 MGI 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8192242 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12968670 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001260 increased body weight IEA N RGD:5509061 20141003 MGI 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12968670 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180503 MGI PMID:26545783 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:16546167 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:12968670 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:12968670 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001411 spinning IAGP N RGD:5509061 20141003 MGI PMID:12968670 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:12968670 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20141003 MGI PMID:8192242 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:8192242 10373 Col2a1 collagen, type II, alpha 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:12968670 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:7276808 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22248926 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151112 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:8192242 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:7276808 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 10373 Col2a1 collagen, type II, alpha 1 gene MP:0002765 short fibula IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003109 short femur IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003109 short femur IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20180503 MGI PMID:26545783 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20141003 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004282 retrognathia IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004351 short humerus IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004351 short humerus IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004355 short radius IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004356 radius hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004359 short ulna IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20180503 MGI PMID:26545783 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004667 vertebral body hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004669 enlarged vertebral body IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004669 enlarged vertebral body IAGP N RGD:5509061 20141003 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:8192242 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:9832566 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:7276808 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:8989518 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004708 short lumbar vertebrae IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004711 persistence of notochord tissue IAGP N RGD:5509061 20141003 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004711 persistence of notochord tissue IAGP N RGD:5509061 20141003 MGI PMID:9832566 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16546167 10373 Col2a1 collagen, type II, alpha 1 gene MP:0005195 abnormal posterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16546167 10373 Col2a1 collagen, type II, alpha 1 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0005458 increased percent body fat/body weight IEA N RGD:5509061 20141003 MGI 10373 Col2a1 collagen, type II, alpha 1 gene MP:0005459 decreased percent body fat/body weight IEA N RGD:5509061 20141003 MGI 10373 Col2a1 collagen, type II, alpha 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0005525 increased renal plasma flow rate IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0006198 enophthalmos IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0006290 proboscis IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:12968670 10373 Col2a1 collagen, type II, alpha 1 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20180503 MGI PMID:26545783 10373 Col2a1 collagen, type II, alpha 1 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0008069 abnormal joint mobility IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0008159 increased diameter of fibula IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0008160 increased diameter of humerus IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0008161 increased diameter of radius IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0008162 increased diameter of tibia IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0008163 increased diameter of ulna IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20160609 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20160609 MGI PMID:12814946 10373 Col2a1 collagen, type II, alpha 1 gene MP:0008736 micromelia IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0009882 absent palatal shelf IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:8989518 10373 Col2a1 collagen, type II, alpha 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7276808 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20151008 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8192242 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180503 MGI PMID:26545783 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7276808 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011175 platyspondylia IAGP N RGD:5509061 20141003 MGI PMID:21538020 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011175 platyspondylia IAGP N RGD:5509061 20180503 MGI PMID:26545783 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011504 abnormal limb long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011504 abnormal limb long bone morphology IAGP N RGD:5509061 20160609 MGI PMID:25541700 10373 Col2a1 collagen, type II, alpha 1 gene MP:0011812 increased cranium length IEA N RGD:5509061 20171123 MGI 10373 Col2a1 collagen, type II, alpha 1 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0013817 absent nasal cavity IAGP N RGD:5509061 20171026 MGI PMID:20730911 10373 Col2a1 collagen, type II, alpha 1 gene MP:0013945 abnormal elbow joint morphology IAGP N RGD:5509061 20181025 MGI PMID:22028304 10373 Col2a1 collagen, type II, alpha 1 gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:15132997 10373 Col2a1 collagen, type II, alpha 1 gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20180503 MGI PMID:26545783 10373 Col2a1 collagen, type II, alpha 1 gene MP:0014164 abnormal ciliary process morphology IAGP N RGD:5509061 20160414 MGI PMID:16546167 10373 Col2a1 collagen, type II, alpha 1 gene MP:0014291 decreased autopod size IAGP N RGD:5509061 20230824 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0014321 short forelimb IEA N RGD:5509061 20231130 MGI 10373 Col2a1 collagen, type II, alpha 1 gene MP:0014430 decreased hyaluronic acid level IAGP N RGD:5509061 20240425 MGI PMID:16546167 10373 Col2a1 collagen, type II, alpha 1 gene MP:0030049 prominent forehead IAGP N RGD:5509061 20170921 MGI PMID:7590256 10373 Col2a1 collagen, type II, alpha 1 gene MP:0030384 short facial bone IAGP N RGD:5509061 20171207 MGI PMID:11680679 10373 Col2a1 collagen, type II, alpha 1 gene MP:0030384 short facial bone IAGP N RGD:5509061 20171207 MGI PMID:24475193 10373 Col2a1 collagen, type II, alpha 1 gene MP:0030384 short facial bone IAGP N RGD:5509061 20171207 MGI PMID:7590256 10374 Comp cartilage oligomeric matrix protein gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:22006726 10374 Comp cartilage oligomeric matrix protein gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17588960 10374 Comp cartilage oligomeric matrix protein gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22006726 10374 Comp cartilage oligomeric matrix protein gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17588960 10374 Comp cartilage oligomeric matrix protein gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:19808781 10374 Comp cartilage oligomeric matrix protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17588960 10374 Comp cartilage oligomeric matrix protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22006726 10374 Comp cartilage oligomeric matrix protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12024046 10374 Comp cartilage oligomeric matrix protein gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:17588960 10374 Comp cartilage oligomeric matrix protein gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:22006726 10374 Comp cartilage oligomeric matrix protein gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:17588960 10374 Comp cartilage oligomeric matrix protein gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:22006726 10374 Comp cartilage oligomeric matrix protein gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22006726 10374 Comp cartilage oligomeric matrix protein gene MP:0003098 decreased tendon stiffness IAGP N RGD:5509061 20141003 MGI PMID:19808781 10374 Comp cartilage oligomeric matrix protein gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:22006726 10374 Comp cartilage oligomeric matrix protein gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:17588960 10374 Comp cartilage oligomeric matrix protein gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:19808781 10374 Comp cartilage oligomeric matrix protein gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:17588960 10374 Comp cartilage oligomeric matrix protein gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:22006726 10374 Comp cartilage oligomeric matrix protein gene MP:0004507 abnormal ischium morphology IAGP N RGD:5509061 20141003 MGI PMID:17588960 10374 Comp cartilage oligomeric matrix protein gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17588960 10374 Comp cartilage oligomeric matrix protein gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22006726 10374 Comp cartilage oligomeric matrix protein gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20160512 MGI PMID:25712208 10374 Comp cartilage oligomeric matrix protein gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:19808781 10374 Comp cartilage oligomeric matrix protein gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:19808781 10374 Comp cartilage oligomeric matrix protein gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22006726 10374 Comp cartilage oligomeric matrix protein gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19808781 10374 Comp cartilage oligomeric matrix protein gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:17588960 10374 Comp cartilage oligomeric matrix protein gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20171221 MGI PMID:17588960 10374 Comp cartilage oligomeric matrix protein gene MP:0030829 abnormal hip joint morphology IAGP N RGD:5509061 20181025 MGI PMID:17588960 10374 Comp cartilage oligomeric matrix protein gene MP:0030829 abnormal hip joint morphology IAGP N RGD:5509061 20181025 MGI PMID:22006726 10378 Comt catechol-O-methyltransferase gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:18469803 10378 Comt catechol-O-methyltransferase gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:9707588 10378 Comt catechol-O-methyltransferase gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:9707588 10378 Comt catechol-O-methyltransferase gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210128 MGI 10378 Comt catechol-O-methyltransferase gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 10378 Comt catechol-O-methyltransferase gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 10378 Comt catechol-O-methyltransferase gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20151001 MGI PMID:24509724 10378 Comt catechol-O-methyltransferase gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20151001 MGI PMID:24509724 10378 Comt catechol-O-methyltransferase gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 10378 Comt catechol-O-methyltransferase gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:18469803 10378 Comt catechol-O-methyltransferase gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18469803 10378 Comt catechol-O-methyltransferase gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:19930170 10378 Comt catechol-O-methyltransferase gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:9707588 10378 Comt catechol-O-methyltransferase gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:18469803 10378 Comt catechol-O-methyltransferase gene MP:0002294 short gestation period IAGP N RGD:5509061 20141003 MGI PMID:18469803 10378 Comt catechol-O-methyltransferase gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20151001 MGI PMID:24509724 10378 Comt catechol-O-methyltransferase gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20151001 MGI PMID:24509724 10378 Comt catechol-O-methyltransferase gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:18469803 10378 Comt catechol-O-methyltransferase gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20160421 MGI 10378 Comt catechol-O-methyltransferase gene MP:0003106 abnormal fear-related response IAGP N RGD:5509061 20151001 MGI PMID:24509724 10378 Comt catechol-O-methyltransferase gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:18469803 10378 Comt catechol-O-methyltransferase gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:20618449 10378 Comt catechol-O-methyltransferase gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18469803 10378 Comt catechol-O-methyltransferase gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18469803 10378 Comt catechol-O-methyltransferase gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160421 MGI 10378 Comt catechol-O-methyltransferase gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:18469803 10378 Comt catechol-O-methyltransferase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:18469803 10378 Comt catechol-O-methyltransferase gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160421 MGI 10378 Comt catechol-O-methyltransferase gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 10378 Comt catechol-O-methyltransferase gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20151001 MGI PMID:24509724 10378 Comt catechol-O-methyltransferase gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20190207 MGI PMID:27388330 10378 Comt catechol-O-methyltransferase gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18469803 10378 Comt catechol-O-methyltransferase gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:19930170 10378 Comt catechol-O-methyltransferase gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20151001 MGI PMID:24509724 10378 Comt catechol-O-methyltransferase gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20151001 MGI PMID:24509724 10378 Comt catechol-O-methyltransferase gene MP:0009394 increased uterine NK cell number IAGP N RGD:5509061 20141003 MGI PMID:18469803 10378 Comt catechol-O-methyltransferase gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20151001 MGI PMID:24509724 10378 Comt catechol-O-methyltransferase gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20151001 MGI PMID:24509724 10378 Comt catechol-O-methyltransferase gene MP:0009455 enhanced cued conditioning behavior IAGP N RGD:5509061 20151001 MGI PMID:24509724 10378 Comt catechol-O-methyltransferase gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20151001 MGI PMID:24509724 10378 Comt catechol-O-methyltransferase gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18469803 10378 Comt catechol-O-methyltransferase gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:18469803 10378 Comt catechol-O-methyltransferase gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 10378 Comt catechol-O-methyltransferase gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20160421 MGI 10378 Comt catechol-O-methyltransferase gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20190207 MGI PMID:27388330 10378 Comt catechol-O-methyltransferase gene MP:0014114 abnormal cognition IAGP N RGD:5509061 20190207 MGI PMID:27388330 10378 Comt catechol-O-methyltransferase gene MP:0014115 cognitive inflexibility IAGP N RGD:5509061 20190207 MGI PMID:27388330 10378 Comt catechol-O-methyltransferase gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 10379 Coq7 demethyl-Q 7 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11716496 10379 Coq7 demethyl-Q 7 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:23847050 10379 Coq7 demethyl-Q 7 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:11716496 10379 Coq7 demethyl-Q 7 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11716496 10379 Coq7 demethyl-Q 7 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:16195414 10379 Coq7 demethyl-Q 7 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11585841 10379 Coq7 demethyl-Q 7 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11716496 10379 Coq7 demethyl-Q 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23847050 10379 Coq7 demethyl-Q 7 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11585841 10379 Coq7 demethyl-Q 7 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:11716496 10379 Coq7 demethyl-Q 7 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:11716496 10379 Coq7 demethyl-Q 7 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20190926 MGI PMID:23045551 10379 Coq7 demethyl-Q 7 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:23847050 10379 Coq7 demethyl-Q 7 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:11716496 10379 Coq7 demethyl-Q 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11585841 10379 Coq7 demethyl-Q 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11716496 10379 Coq7 demethyl-Q 7 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23847050 10379 Coq7 demethyl-Q 7 gene MP:0012556 increased cell death IAGP N RGD:5509061 20141003 MGI PMID:23847050 10380 Cort cortistatin gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:21971153 10380 Cort cortistatin gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:21971153 10380 Cort cortistatin gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 10380 Cort cortistatin gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:21971153 10380 Cort cortistatin gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:21971153 10380 Cort cortistatin gene MP:0005129 increased adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:21971153 10380 Cort cortistatin gene MP:0005138 decreased prolactin level IAGP N RGD:5509061 20141003 MGI PMID:21971153 10380 Cort cortistatin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21971153 10380 Cort cortistatin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21971153 10380 Cort cortistatin gene MP:0011067 abnormal somatostatin level IAGP N RGD:5509061 20141003 MGI PMID:21971153 10380 Cort cortistatin gene MP:0011612 increased circulating ghrelin level IAGP N RGD:5509061 20141003 MGI PMID:21971153 10381 Cox6a1 cytochrome c oxidase subunit 6A1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20161103 MGI PMID:25152455 10381 Cox6a1 cytochrome c oxidase subunit 6A1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20161103 MGI PMID:25152455 10381 Cox6a1 cytochrome c oxidase subunit 6A1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20161103 MGI PMID:25152455 10381 Cox6a1 cytochrome c oxidase subunit 6A1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20161103 MGI PMID:25152455 10381 Cox6a1 cytochrome c oxidase subunit 6A1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20161103 MGI PMID:25152455 10381 Cox6a1 cytochrome c oxidase subunit 6A1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20161103 MGI PMID:25152455 10381 Cox6a1 cytochrome c oxidase subunit 6A1 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20161103 MGI PMID:25152455 10382 Cox6a2 cytochrome c oxidase subunit 6A2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11788423 10382 Cox6a2 cytochrome c oxidase subunit 6A2 gene MP:0004011 decreased diastolic filling velocity IAGP N RGD:5509061 20141003 MGI PMID:11788423 10384 Cp ceruloplasmin gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12393173 10384 Cp ceruloplasmin gene MP:0000828 abnormal fourth ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16988052 10384 Cp ceruloplasmin gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16988052 10384 Cp ceruloplasmin gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12151537 10384 Cp ceruloplasmin gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:19036966 10384 Cp ceruloplasmin gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19036966 10384 Cp ceruloplasmin gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:15365174 10384 Cp ceruloplasmin gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:18326691 10384 Cp ceruloplasmin gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:15365174 10384 Cp ceruloplasmin gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:19036966 10384 Cp ceruloplasmin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12151537 10384 Cp ceruloplasmin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18804145 10384 Cp ceruloplasmin gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22342521 10384 Cp ceruloplasmin gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:10485908 10384 Cp ceruloplasmin gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:15365174 10384 Cp ceruloplasmin gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:18326691 10384 Cp ceruloplasmin gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:22342521 10384 Cp ceruloplasmin gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:18326691 10384 Cp ceruloplasmin gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IEA N RGD:5509061 20220519 MGI 10384 Cp ceruloplasmin gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12151537 10384 Cp ceruloplasmin gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18804145 10384 Cp ceruloplasmin gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16988052 10384 Cp ceruloplasmin gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22342521 10384 Cp ceruloplasmin gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 10384 Cp ceruloplasmin gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:12393173 10384 Cp ceruloplasmin gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 10384 Cp ceruloplasmin gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210520 MGI 10384 Cp ceruloplasmin gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12151537 10384 Cp ceruloplasmin gene MP:0003043 hypoalgesia IEA N RGD:5509061 20220519 MGI 10384 Cp ceruloplasmin gene MP:0003065 abnormal liver copper level IAGP N RGD:5509061 20141003 MGI PMID:11461924 10384 Cp ceruloplasmin gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:12151537 10384 Cp ceruloplasmin gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:18804145 10384 Cp ceruloplasmin gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12151537 10384 Cp ceruloplasmin gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:12151537 10384 Cp ceruloplasmin gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:12393173 10384 Cp ceruloplasmin gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:22342521 10384 Cp ceruloplasmin gene MP:0005098 abnormal optic choroid morphology IAGP N RGD:5509061 20141003 MGI PMID:15365174 10384 Cp ceruloplasmin gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15365174 10384 Cp ceruloplasmin gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:19036966 10384 Cp ceruloplasmin gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15365174 10384 Cp ceruloplasmin gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18326691 10384 Cp ceruloplasmin gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22342521 10384 Cp ceruloplasmin gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:18326691 10384 Cp ceruloplasmin gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20141003 MGI PMID:22342521 10384 Cp ceruloplasmin gene MP:0005549 retina pigment epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15365174 10384 Cp ceruloplasmin gene MP:0005549 retina pigment epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18326691 10384 Cp ceruloplasmin gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 10384 Cp ceruloplasmin gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10485908 10384 Cp ceruloplasmin gene MP:0005638 hemochromatosis IAGP N RGD:5509061 20141003 MGI PMID:17258727 10384 Cp ceruloplasmin gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210520 MGI 10384 Cp ceruloplasmin gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12393173 10384 Cp ceruloplasmin gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:12151537 10384 Cp ceruloplasmin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:15365174 10384 Cp ceruloplasmin gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20141003 MGI PMID:22342521 10384 Cp ceruloplasmin gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:10485908 10384 Cp ceruloplasmin gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:11461924 10384 Cp ceruloplasmin gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:12151537 10384 Cp ceruloplasmin gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:12393173 10384 Cp ceruloplasmin gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:10485908 10384 Cp ceruloplasmin gene MP:0008811 abnormal brain iron level IAGP N RGD:5509061 20141003 MGI PMID:12151537 10384 Cp ceruloplasmin gene MP:0008811 abnormal brain iron level IAGP N RGD:5509061 20141003 MGI PMID:16988052 10384 Cp ceruloplasmin gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:15365174 10384 Cp ceruloplasmin gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:18326691 10384 Cp ceruloplasmin gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:12743117 10384 Cp ceruloplasmin gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20160421 MGI 10384 Cp ceruloplasmin gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20141003 MGI PMID:10485908 10384 Cp ceruloplasmin gene MP:0011896 increased circulating unsaturated transferrin level IAGP N RGD:5509061 20141003 MGI PMID:12151537 10384 Cp ceruloplasmin gene MP:0012661 decreased circulating ceruloplasmin level IAGP N RGD:5509061 20141003 MGI PMID:10485908 10384 Cp ceruloplasmin gene MP:0014175 abnormal ciliary epithelium morphology IAGP N RGD:5509061 20160505 MGI PMID:18326691 10384 Cp ceruloplasmin gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:18326691 10388 Cpd carboxypeptidase D gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20220519 MGI 10388 Cpd carboxypeptidase D gene MP:0003717 pallor IEA N RGD:5509061 20220519 MGI 10388 Cpd carboxypeptidase D gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20220811 MGI 10388 Cpd carboxypeptidase D gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210826 MGI 10388 Cpd carboxypeptidase D gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 10388 Cpd carboxypeptidase D gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 10388 Cpd carboxypeptidase D gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 10389 Cps1 carbamoyl-phosphate synthetase 1 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20181227 MGI 10389 Cps1 carbamoyl-phosphate synthetase 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 10389 Cps1 carbamoyl-phosphate synthetase 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 10389 Cps1 carbamoyl-phosphate synthetase 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 10389 Cps1 carbamoyl-phosphate synthetase 1 gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:9862865 10389 Cps1 carbamoyl-phosphate synthetase 1 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20211021 MGI 10389 Cps1 carbamoyl-phosphate synthetase 1 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20210128 MGI 10389 Cps1 carbamoyl-phosphate synthetase 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20221215 MGI 10389 Cps1 carbamoyl-phosphate synthetase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9862865 10389 Cps1 carbamoyl-phosphate synthetase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10390 Cpt1a carnitine palmitoyltransferase 1a, liver gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16169268 10390 Cpt1a carnitine palmitoyltransferase 1a, liver gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20160609 MGI PMID:25830893 10390 Cpt1a carnitine palmitoyltransferase 1a, liver gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20160804 MGI PMID:16169268 10390 Cpt1a carnitine palmitoyltransferase 1a, liver gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16169268 10390 Cpt1a carnitine palmitoyltransferase 1a, liver gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16169268 10390 Cpt1a carnitine palmitoyltransferase 1a, liver gene MP:0020316 decreased vascular endothelial cell proliferation IAGP N RGD:5509061 20160616 MGI PMID:25830893 10391 Cpt1b carnitine palmitoyltransferase 1b, muscle gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:18023382 10391 Cpt1b carnitine palmitoyltransferase 1b, muscle gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18023382 10392 Cpt2 carnitine palmitoyltransferase 2 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20160421 MGI 10392 Cpt2 carnitine palmitoyltransferase 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20160421 MGI 10392 Cpt2 carnitine palmitoyltransferase 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170504 MGI 10392 Cpt2 carnitine palmitoyltransferase 2 gene MP:0002282 abnormal trachea morphology IEA N RGD:5509061 20170504 MGI 10392 Cpt2 carnitine palmitoyltransferase 2 gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 10392 Cpt2 carnitine palmitoyltransferase 2 gene MP:0005244 hemopericardium IEA N RGD:5509061 20170504 MGI 10392 Cpt2 carnitine palmitoyltransferase 2 gene MP:0010439 abnormal hepatic vein morphology IEA N RGD:5509061 20170504 MGI 10392 Cpt2 carnitine palmitoyltransferase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 10392 Cpt2 carnitine palmitoyltransferase 2 gene MP:0013852 abnormal Mullerian duct topology IEA N RGD:5509061 20170504 MGI 10392 Cpt2 carnitine palmitoyltransferase 2 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 10395 Crmp1 collapsin response mediator protein 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 10395 Crmp1 collapsin response mediator protein 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 10395 Crmp1 collapsin response mediator protein 1 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17182786 10395 Crmp1 collapsin response mediator protein 1 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 10395 Crmp1 collapsin response mediator protein 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17344389 10395 Crmp1 collapsin response mediator protein 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 10395 Crmp1 collapsin response mediator protein 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 10395 Crmp1 collapsin response mediator protein 1 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17344389 10395 Crmp1 collapsin response mediator protein 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 10395 Crmp1 collapsin response mediator protein 1 gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 10395 Crmp1 collapsin response mediator protein 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:17121542 10395 Crmp1 collapsin response mediator protein 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17121542 10395 Crmp1 collapsin response mediator protein 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17182786 10395 Crmp1 collapsin response mediator protein 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22279220 10395 Crmp1 collapsin response mediator protein 1 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17344389 10395 Crmp1 collapsin response mediator protein 1 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22279220 10396 Dpysl4 dihydropyrimidinase-like 4 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17785607 10396 Dpysl4 dihydropyrimidinase-like 4 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:17785607 10396 Dpysl4 dihydropyrimidinase-like 4 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:17785607 10396 Dpysl4 dihydropyrimidinase-like 4 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:17785607 10396 Dpysl4 dihydropyrimidinase-like 4 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17785607 10397 Dpysl3 dihydropyrimidinase-like 3 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20201015 MGI PMID:25225289 10397 Dpysl3 dihydropyrimidinase-like 3 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20201015 MGI PMID:25225289 10397 Dpysl3 dihydropyrimidinase-like 3 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20160324 MGI PMID:22234963 10397 Dpysl3 dihydropyrimidinase-like 3 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20201015 MGI PMID:25225289 10397 Dpysl3 dihydropyrimidinase-like 3 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20160324 MGI PMID:22234963 10397 Dpysl3 dihydropyrimidinase-like 3 gene MP:0009970 increased hippocampus pyramidal cell number IAGP N RGD:5509061 20160324 MGI PMID:22234963 10397 Dpysl3 dihydropyrimidinase-like 3 gene MP:0012458 decreased hippocampus pyramidal cell length IAGP N RGD:5509061 20160324 MGI PMID:22234963 10398 Crp C-reactive protein, pentraxin-related gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21149301 10398 Crp C-reactive protein, pentraxin-related gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21149301 10398 Crp C-reactive protein, pentraxin-related gene MP:0000203 abnormal circulating aspartate transaminase level IAGP N RGD:5509061 20231116 MGI PMID:34536564 10398 Crp C-reactive protein, pentraxin-related gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20231116 MGI PMID:34536564 10398 Crp C-reactive protein, pentraxin-related gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21149301 10398 Crp C-reactive protein, pentraxin-related gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21149301 10398 Crp C-reactive protein, pentraxin-related gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21149301 10398 Crp C-reactive protein, pentraxin-related gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20231116 MGI PMID:34536564 10398 Crp C-reactive protein, pentraxin-related gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21149301 10398 Crp C-reactive protein, pentraxin-related gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20231116 MGI PMID:34536564 10398 Crp C-reactive protein, pentraxin-related gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21149301 10398 Crp C-reactive protein, pentraxin-related gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:21149301 10398 Crp C-reactive protein, pentraxin-related gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:21149301 10398 Crp C-reactive protein, pentraxin-related gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20231116 MGI PMID:34536564 10398 Crp C-reactive protein, pentraxin-related gene MP:0031060 decreased circulating C-reactive protein level IAGP N RGD:5509061 20200618 MGI PMID:21149301 10400 Cryab crystallin, alpha B gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:21445271 10400 Cryab crystallin, alpha B gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:21445271 10400 Cryab crystallin, alpha B gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:21445271 10400 Cryab crystallin, alpha B gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:23872361 10400 Cryab crystallin, alpha B gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:21445271 10400 Cryab crystallin, alpha B gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:21445271 10400 Cryab crystallin, alpha B gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20240118 MGI PMID:37435054 10400 Cryab crystallin, alpha B gene MP:0002579 disorganized secondary lens fibers IAGP N RGD:5509061 20141003 MGI PMID:21445271 10400 Cryab crystallin, alpha B gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23872361 10400 Cryab crystallin, alpha B gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20240118 MGI PMID:37435054 10400 Cryab crystallin, alpha B gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23872361 10400 Cryab crystallin, alpha B gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20240118 MGI PMID:37435054 10400 Cryab crystallin, alpha B gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20240118 MGI PMID:37435054 10400 Cryab crystallin, alpha B gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20240118 MGI PMID:37435054 10400 Cryab crystallin, alpha B gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:21445271 10400 Cryab crystallin, alpha B gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:21445271 10400 Cryab crystallin, alpha B gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21445271 10400 Cryab crystallin, alpha B gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:21445271 10400 Cryab crystallin, alpha B gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20240118 MGI PMID:37435054 10400 Cryab crystallin, alpha B gene MP:0030938 abnormal reticulophagy IAGP N RGD:5509061 20190711 MGI PMID:23872361 10401 Crybb1 crystallin, beta B1 gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20231207 MGI 10401118 Pgia39_m proteoglycan induced arthritis 39 (mouse) qtl MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20151001 MGI PMID:12794840 10401118 Pgia39_m proteoglycan induced arthritis 39 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20151001 MGI PMID:12794840 10401118 Pgia39_m proteoglycan induced arthritis 39 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150925 MGI Created by mouse qtl pipeline PMID:12794840 10401118 Pgia39_m proteoglycan induced arthritis 39 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20150925 MGI Created by mouse qtl pipeline PMID:12794840 10401904 Sicd4_m seizure-induced cell death 4 (mouse) qtl MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20151015 MGI PMID:17996456 10401904 Sicd4_m seizure-induced cell death 4 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20151009 MGI Created by mouse qtl pipeline PMID:17996456 10402412 Rmp6_m resistance to mousepox 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20151023 MGI Created by mouse qtl pipeline PMID:1433507 10402412 Rmp6_m resistance to mousepox 6 (mouse) qtl MP:0020929 decreased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:1433507 10402413 Rmp5_m resistance to mousepox 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20151023 MGI Created by mouse qtl pipeline PMID:1433507 10402413 Rmp5_m resistance to mousepox 5 (mouse) qtl MP:0020929 decreased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:1433507 10402414 Sgp5_m serum gp70 production 5 (mouse) qtl MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20151029 MGI PMID:15634937 10402414 Sgp5_m serum gp70 production 5 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20151029 MGI PMID:15634937 10402414 Sgp5_m serum gp70 production 5 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20151023 MGI Created by mouse qtl pipeline PMID:15634937 10402414 Sgp5_m serum gp70 production 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20151023 MGI Created by mouse qtl pipeline PMID:15634937 10402414 Sgp5_m serum gp70 production 5 (mouse) qtl MP:0005615 increased susceptibility to type III hypersensitivity reaction IAGP N RGD:5509061 20151029 MGI PMID:15634937 10406 Cryga crystallin, gamma A gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:7088001 10406 Cryga crystallin, gamma A gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15037589 10406 Cryga crystallin, gamma A gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20141003 MGI PMID:15037589 10406 Cryga crystallin, gamma A gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:15037589 10406 Cryga crystallin, gamma A gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:6510713 10406 Cryga crystallin, gamma A gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:6877261 10406 Cryga crystallin, gamma A gene MP:0010263 total cataract IAGP N RGD:5509061 20141003 MGI PMID:7088001 10406 Cryga crystallin, gamma A gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:15037589 10406 Cryga crystallin, gamma A gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:7088001 10407 Crygb crystallin, gamma B gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:18172107 10407 Crygb crystallin, gamma B gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20171221 MGI PMID:20844585 10407 Crygb crystallin, gamma B gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18172107 10407 Crygb crystallin, gamma B gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20180628 MGI PMID:20844585 10407 Crygb crystallin, gamma B gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:18172107 10407 Crygb crystallin, gamma B gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:6479248 10407 Crygb crystallin, gamma B gene MP:0010262 lamellar cataract IAGP N RGD:5509061 20141003 MGI PMID:15878859 10408 Crygc crystallin, gamma C gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 10408 Crygc crystallin, gamma C gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11773036 10408 Crygc crystallin, gamma C gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:15037589 10408 Crygc crystallin, gamma C gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:20686773 10408 Crygc crystallin, gamma C gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20231130 MGI PMID:37331601 10408 Crygc crystallin, gamma C gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:11773036 10408 Crygc crystallin, gamma C gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:15037589 10408 Crygc crystallin, gamma C gene MP:0001304 cataract IAGP N RGD:5509061 20231130 MGI PMID:37331601 10408 Crygc crystallin, gamma C gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:20686773 10408 Crygc crystallin, gamma C gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210128 MGI 10408 Crygc crystallin, gamma C gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:20686773 10408 Crygc crystallin, gamma C gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15037589 10408 Crygc crystallin, gamma C gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20231130 MGI PMID:37331601 10408 Crygc crystallin, gamma C gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20686773 10408 Crygc crystallin, gamma C gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:20686773 10408 Crygc crystallin, gamma C gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:20686773 10408 Crygc crystallin, gamma C gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20231130 MGI PMID:37331601 10408 Crygc crystallin, gamma C gene MP:0010255 cortical cataract IEA N RGD:5509061 20190905 MGI 10408 Crygc crystallin, gamma C gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 10408 Crygc crystallin, gamma C gene MP:0031345 developmental cataract IAGP N RGD:5509061 20220217 MGI PMID:20686773 10409 Crygd crystallin, gamma D gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:15037589 10409 Crygd crystallin, gamma D gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:10704279 10409 Crygd crystallin, gamma D gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:15037589 10409 Crygd crystallin, gamma D gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:15037589 10409 Crygd crystallin, gamma D gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:17652744 10409 Crygd crystallin, gamma D gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15037589 10409 Crygd crystallin, gamma D gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17652744 10409 Crygd crystallin, gamma D gene MP:0006225 ocular rupture IAGP N RGD:5509061 20141003 MGI PMID:17652744 10409 Crygd crystallin, gamma D gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:12226711 10409 Crygd crystallin, gamma D gene MP:0010263 total cataract IAGP N RGD:5509061 20141003 MGI PMID:17652744 10409 Crygd crystallin, gamma D gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:15037589 10410 Cryge crystallin, gamma E gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10932192 10410 Cryge crystallin, gamma E gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:1511869 10410 Cryge crystallin, gamma E gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:3209064 10410 Cryge crystallin, gamma E gene MP:0001297 microphthalmia IAGP N RGD:5509061 20150409 MGI PMID:1973159 10410 Cryge crystallin, gamma E gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:15037589 10410 Cryge crystallin, gamma E gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:3209064 10410 Cryge crystallin, gamma E gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:7011824 10410 Cryge crystallin, gamma E gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20150409 MGI PMID:1973159 10410 Cryge crystallin, gamma E gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:10932192 10410 Cryge crystallin, gamma E gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:12196406 10410 Cryge crystallin, gamma E gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:15037589 10410 Cryge crystallin, gamma E gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:1511869 10410 Cryge crystallin, gamma E gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:17223009 10410 Cryge crystallin, gamma E gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:3209064 10410 Cryge crystallin, gamma E gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:7035547 10410 Cryge crystallin, gamma E gene MP:0001304 cataract IAGP N RGD:5509061 20150409 MGI PMID:1973159 10410 Cryge crystallin, gamma E gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:7215463 10410 Cryge crystallin, gamma E gene MP:0001320 small pupil IAGP N RGD:5509061 20141003 MGI PMID:3209064 10410 Cryge crystallin, gamma E gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:3209064 10410 Cryge crystallin, gamma E gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12196406 10410 Cryge crystallin, gamma E gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15037589 10410 Cryge crystallin, gamma E gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:7215463 10410 Cryge crystallin, gamma E gene MP:0003236 abnormal lens capsule morphology IAGP N RGD:5509061 20150409 MGI PMID:1973159 10410 Cryge crystallin, gamma E gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:1811943 10410 Cryge crystallin, gamma E gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20150409 MGI PMID:1973159 10410 Cryge crystallin, gamma E gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20150514 MGI PMID:7035547 10410 Cryge crystallin, gamma E gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20150409 MGI PMID:1973159 10410 Cryge crystallin, gamma E gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:17223009 10410 Cryge crystallin, gamma E gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20150514 MGI PMID:7035547 10410 Cryge crystallin, gamma E gene MP:0010263 total cataract IAGP N RGD:5509061 20141003 MGI PMID:3209064 10410 Cryge crystallin, gamma E gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:1511869 10410 Cryge crystallin, gamma E gene MP:0013731 immature cataract IAGP N RGD:5509061 20150514 MGI PMID:1973159 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16823860 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000064 failure of bone resorption IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:16823860 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0000921 demyelination IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16823860 10412 Csf1r colony stimulating factor 1 receptor gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0001393 ataxia IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16823860 10412 Csf1r colony stimulating factor 1 receptor gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151022 MGI PMID:16823860 10412 Csf1r colony stimulating factor 1 receptor gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0003064 decreased coping response IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16444257 10412 Csf1r colony stimulating factor 1 receptor gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16823860 10412 Csf1r colony stimulating factor 1 receptor gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20141003 MGI PMID:16444257 10412 Csf1r colony stimulating factor 1 receptor gene MP:0008118 absent Langerhans cell IAGP N RGD:5509061 20141003 MGI PMID:16444257 10412 Csf1r colony stimulating factor 1 receptor gene MP:0008119 decreased Langerhans cell number IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0008918 microgliosis IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0010050 hypermyelination IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0010892 increased oligodendrocyte progenitor number IAGP N RGD:5509061 20160915 MGI PMID:25497733 10412 Csf1r colony stimulating factor 1 receptor gene MP:0010970 abnormal compact bone lamellar structure IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0014269 decreased testes secretion IAGP N RGD:5509061 20230810 MGI PMID:11756160 10412 Csf1r colony stimulating factor 1 receptor gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0030188 round snout IAGP N RGD:5509061 20171019 MGI PMID:16823860 10412 Csf1r colony stimulating factor 1 receptor gene MP:0030487 abnormal osteocyte dendritic process morphology IAGP N RGD:5509061 20171221 MGI PMID:15312244 10412 Csf1r colony stimulating factor 1 receptor gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:16823860 10412067 Pain2_m pain 2 (mouse) qtl MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20151119 MGI PMID:17686043 10412067 Pain2_m pain 2 (mouse) qtl MP:0003177 allodynia IAGP N RGD:5509061 20151119 MGI PMID:15979798 10412067 Pain2_m pain 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20151113 MGI Created by mouse qtl pipeline PMID:15979798 10412067 Pain2_m pain 2 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20151113 MGI Created by mouse qtl pipeline PMID:15979798 10412068 Pbrbc4_m peripheral blood RBC 4 (mouse) qtl MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20151119 MGI PMID:17185011 10412068 Pbrbc4_m peripheral blood RBC 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20151113 MGI Created by mouse qtl pipeline PMID:17185011 10412126 Ril4_m radiation-induced leukemia sensitivity 4 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20151113 MGI Created by mouse qtl pipeline PMID:6300845 10412126 Ril4_m radiation-induced leukemia sensitivity 4 (mouse) qtl MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20151119 MGI PMID:6300845 10412185 Hcs9_m hepatocarcinogenesis susceptibility 9 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20151113 MGI Created by mouse qtl pipeline PMID:15238534 10412185 Hcs9_m hepatocarcinogenesis susceptibility 9 (mouse) qtl MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20151119 MGI PMID:15238534 10412185 Hcs9_m hepatocarcinogenesis susceptibility 9 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15238534 10412185 Hcs9_m hepatocarcinogenesis susceptibility 9 (mouse) qtl MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20151119 MGI PMID:15238534 10412186 Hcs8_m hepatocarcinogenesis susceptibility 8 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20151113 MGI Created by mouse qtl pipeline PMID:15238534 10412186 Hcs8_m hepatocarcinogenesis susceptibility 8 (mouse) qtl MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20151119 MGI PMID:15238534 10412186 Hcs8_m hepatocarcinogenesis susceptibility 8 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15238534 10412186 Hcs8_m hepatocarcinogenesis susceptibility 8 (mouse) qtl MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20151119 MGI PMID:15238534 10412244 Par5_m pulmonary adenoma resistance 5 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20160729 MGI Created by mouse qtl pipeline PMID:9331067 10412244 Par5_m pulmonary adenoma resistance 5 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20241101 MGI Created by mouse qtl pipeline PMID:9331067 10412244 Par5_m pulmonary adenoma resistance 5 (mouse) qtl MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20160728 MGI PMID:9331067 10414 Csn1s1 casein alpha s1 gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:21789179 10414 Csn1s1 casein alpha s1 gene MP:0013716 hypolactation IAGP N RGD:5509061 20150402 MGI PMID:21789179 10414 Csn1s1 casein alpha s1 gene MP:0020880 abnormal milk calcium level IAGP N RGD:5509061 20191226 MGI PMID:21789179 10414 Csn1s1 casein alpha s1 gene MP:0020886 abnormal milk phosphate level IAGP N RGD:5509061 20191226 MGI PMID:21789179 10415 Cst3 cystatin C gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141016 MGI PMID:24500719 10415 Cst3 cystatin C gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 10415 Cst3 cystatin C gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:10748866 10415 Cst3 cystatin C gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141016 MGI PMID:24500719 10415 Cst3 cystatin C gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141016 MGI PMID:24500719 10415 Cst3 cystatin C gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:15450354 10415 Cst3 cystatin C gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15653570 10415 Cst3 cystatin C gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:15653570 10415 Cst3 cystatin C gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15653570 10415 Cst3 cystatin C gene MP:0005489 vascular smooth muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15653570 10415 Cst3 cystatin C gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:15653570 10415 Cst3 cystatin C gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:15450354 10415 Cst3 cystatin C gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:15450354 10415 Cst3 cystatin C gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141016 MGI PMID:24500719 10415 Cst3 cystatin C gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15653570 10415 Cst3 cystatin C gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:15653570 10415 Cst3 cystatin C gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20200102 MGI PMID:24500719 10417 Cstb cystatin B gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20181227 MGI 10417 Cstb cystatin B gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:12934064 10417 Cstb cystatin B gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:9806543 10417 Cstb cystatin B gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12934064 10417 Cstb cystatin B gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9806543 10417 Cstb cystatin B gene MP:0001258 decreased body length IEA N RGD:5509061 20181227 MGI 10417 Cstb cystatin B gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:12934064 10417 Cstb cystatin B gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:9806543 10417 Cstb cystatin B gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:9806543 10417 Cstb cystatin B gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:9806543 10417 Cstb cystatin B gene MP:0001316 cornea scarring IAGP N RGD:5509061 20141003 MGI PMID:12934064 10417 Cstb cystatin B gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12934064 10417 Cstb cystatin B gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9806543 10417 Cstb cystatin B gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 10417 Cstb cystatin B gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9806543 10417 Cstb cystatin B gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9806543 10417 Cstb cystatin B gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20201022 MGI 10417 Cstb cystatin B gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9806543 10417 Cstb cystatin B gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:12934064 10417 Cstb cystatin B gene MP:0002574 increased vertical activity IEA N RGD:5509061 20181227 MGI 10417 Cstb cystatin B gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 10417 Cstb cystatin B gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:11555622 10417 Cstb cystatin B gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20201231 MGI 10417 Cstb cystatin B gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12934064 10417 Cstb cystatin B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 10417 Cstb cystatin B gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:12934064 10417 Cstb cystatin B gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 10417 Cstb cystatin B gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:9806543 10417 Cstb cystatin B gene MP:0005515 uveitis IAGP N RGD:5509061 20141003 MGI PMID:9806543 10417 Cstb cystatin B gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20211021 MGI 10417 Cstb cystatin B gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20201231 MGI 10417 Cstb cystatin B gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 10417 Cstb cystatin B gene MP:0030143 facial muscle spasm IAGP N RGD:5509061 20171005 MGI PMID:9806543 10421 Ctsc cathepsin C gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:14966572 10421 Ctsc cathepsin C gene MP:0001511 disheveled coat IEA N RGD:5509061 20111116 MGI 10421 Ctsc cathepsin C gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 10421 Ctsc cathepsin C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20435891 10421 Ctsc cathepsin C gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10411926 10421 Ctsc cathepsin C gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:18292580 10421 Ctsc cathepsin C gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:18292580 10421 Ctsc cathepsin C gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:14966572 10421 Ctsc cathepsin C gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10411926 10421 Ctsc cathepsin C gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:10411926 10421 Ctsc cathepsin C gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:14966572 10421 Ctsc cathepsin C gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18292580 10421 Ctsc cathepsin C gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18292580 10421 Ctsc cathepsin C gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:18292580 10421 Ctsc cathepsin C gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20111116 MGI 10422 Ctse cathepsin E gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:14769879 10422 Ctse cathepsin E gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:14769879 10422 Ctse cathepsin E gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:14769879 10422 Ctse cathepsin E gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:14769879 10422 Ctse cathepsin E gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:14769879 10422 Ctse cathepsin E gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:14769879 10422 Ctse cathepsin E gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:14769879 10422 Ctse cathepsin E gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:18000662 10422 Ctse cathepsin E gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18000662 10422 Ctse cathepsin E gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:18000662 10422 Ctse cathepsin E gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:14769879 10422 Ctse cathepsin E gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:14769879 10422 Ctse cathepsin E gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14769879 10422 Ctse cathepsin E gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:14769879 10422 Ctse cathepsin E gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:14769879 10422 Ctse cathepsin E gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:14769879 10422 Ctse cathepsin E gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:14769879 10423 Ctsh cathepsin H gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 10423 Ctsh cathepsin H gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:23830514 10423 Ctsh cathepsin H gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:22022579 10423 Ctsh cathepsin H gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20435891 10423 Ctsh cathepsin H gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210520 MGI 10423 Ctsh cathepsin H gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20220811 MGI 10423 Ctsh cathepsin H gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 10423 Ctsh cathepsin H gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:22022579 10423 Ctsh cathepsin H gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20240523 MGI 10423 Ctsh cathepsin H gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 10424 Ctsl cathepsin L gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15905545 10424 Ctsl cathepsin L gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0000376 folliculitis IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0000414 alopecia IAGP N RGD:5509061 20161216 MGI PMID:25222295 10424 Ctsl cathepsin L gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:12048238 10424 Ctsl cathepsin L gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:17068745 10424 Ctsl cathepsin L gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12782676 10424 Ctsl cathepsin L gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15905545 10424 Ctsl cathepsin L gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:15905545 10424 Ctsl cathepsin L gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12048238 10424 Ctsl cathepsin L gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12048238 10424 Ctsl cathepsin L gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12533435 10424 Ctsl cathepsin L gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:12048238 10424 Ctsl cathepsin L gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0001219 thick epidermis IAGP N RGD:5509061 20161216 MGI PMID:25222295 10424 Ctsl cathepsin L gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20161216 MGI PMID:25222295 10424 Ctsl cathepsin L gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0001283 sparse vibrissae IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:12048238 10424 Ctsl cathepsin L gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19664906 10424 Ctsl cathepsin L gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20161216 MGI PMID:25222295 10424 Ctsl cathepsin L gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12048238 10424 Ctsl cathepsin L gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:19664906 10424 Ctsl cathepsin L gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0002145 abnormal T cell differentiation IEA N RGD:5509061 20190418 MGI 10424 Ctsl cathepsin L gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:12048238 10424 Ctsl cathepsin L gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12533435 10424 Ctsl cathepsin L gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:15905545 10424 Ctsl cathepsin L gene MP:0002343 abnormal lymph node cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15905545 10424 Ctsl cathepsin L gene MP:0002367 abnormal thymus lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:15905545 10424 Ctsl cathepsin L gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0002626 increased heart rate IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12048238 10424 Ctsl cathepsin L gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0002833 increased heart weight IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12048238 10424 Ctsl cathepsin L gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:12048238 10424 Ctsl cathepsin L gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0003849 greasy coat IAGP N RGD:5509061 20180531 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0003865 lymph node inflammation IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:19664906 10424 Ctsl cathepsin L gene MP:0004085 abnormal heartbeat IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12782676 10424 Ctsl cathepsin L gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:19664906 10424 Ctsl cathepsin L gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12533435 10424 Ctsl cathepsin L gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19664906 10424 Ctsl cathepsin L gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IEA N RGD:5509061 20190418 MGI 10424 Ctsl cathepsin L gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20161216 MGI PMID:25222295 10424 Ctsl cathepsin L gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:12782676 10424 Ctsl cathepsin L gene MP:0005471 decreased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:12782676 10424 Ctsl cathepsin L gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:12782676 10424 Ctsl cathepsin L gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0006033 abnormal external auditory canal morphology IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0006045 mitral valve regurgitation IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15905545 10424 Ctsl cathepsin L gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19664906 10424 Ctsl cathepsin L gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20161216 MGI PMID:25222295 10424 Ctsl cathepsin L gene MP:0008076 abnormal CD4-positive T cell differentiation IEA N RGD:5509061 20190418 MGI 10424 Ctsl cathepsin L gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15905545 10424 Ctsl cathepsin L gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20190418 MGI 10424 Ctsl cathepsin L gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:12048238 10424 Ctsl cathepsin L gene MP:0008726 increased heart left atrium size IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:15905545 10424 Ctsl cathepsin L gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20161216 MGI PMID:25222295 10424 Ctsl cathepsin L gene MP:0009600 hypergranulosis IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20141003 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0010202 focal dorsal hair loss IAGP N RGD:5509061 20141003 MGI PMID:15154914 10424 Ctsl cathepsin L gene MP:0010505 abnormal T wave IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0010688 hair follicle outer root sheath hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 10424 Ctsl cathepsin L gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 10424 Ctsl cathepsin L gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 10424 Ctsl cathepsin L gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10199917 10424 Ctsl cathepsin L gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12048238 10424 Ctsl cathepsin L gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:5563943 10424 Ctsl cathepsin L gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20161216 MGI PMID:25222295 10424 Ctsl cathepsin L gene MP:0011223 dilated lymph node medullary sinus IAGP N RGD:5509061 20141003 MGI PMID:15905545 10424 Ctsl cathepsin L gene MP:0011919 abnormal R wave IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20170817 MGI PMID:11972068 10424 Ctsl cathepsin L gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 10424 Ctsl cathepsin L gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 10424 Ctsl cathepsin L gene MP:0013251 dental pulp necrosis IAGP N RGD:5509061 20180111 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0013593 enlarged thymus cortex IAGP N RGD:5509061 20150326 MGI PMID:15905545 10424 Ctsl cathepsin L gene MP:0030515 periodontal ligament necrosis IAGP N RGD:5509061 20180111 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0030571 dilated piliary canal IAGP N RGD:5509061 20180524 MGI PMID:11023992 10424 Ctsl cathepsin L gene MP:0030571 dilated piliary canal IAGP N RGD:5509061 20180524 MGI PMID:12163394 10424 Ctsl cathepsin L gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:11972068 10425 Cycs cytochrome c, somatic gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0000898 midbrain hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0000919 cranioschisis IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10830166 10425 Cycs cytochrome c, somatic gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10830166 10425 Cycs cytochrome c, somatic gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10830166 10425 Cycs cytochrome c, somatic gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10830166 10425 Cycs cytochrome c, somatic gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:10830166 10425 Cycs cytochrome c, somatic gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10830166 10425 Cycs cytochrome c, somatic gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:15907471 10425 Cycs cytochrome c, somatic gene MP:0030049 prominent forehead IAGP N RGD:5509061 20170921 MGI PMID:15907471 10426 Cyct cytochrome c, testis gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:12101247 10426 Cyct cytochrome c, testis gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12101247 10426 Cyct cytochrome c, testis gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12101247 10426 Cyct cytochrome c, testis gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:12101247 10426 Cyct cytochrome c, testis gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12101247 10426 Cyct cytochrome c, testis gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:12101247 10426 Cyct cytochrome c, testis gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20141003 MGI PMID:12101247 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0000635 pituitary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0003353 decreased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0004119 hypokalemia IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0009078 adrenal gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0009082 uterus cyst IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0009221 uterus adenomyosis IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0011541 decreased urine aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0011546 increased urine progesterone level IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0011550 decreased urine corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0011553 increased urine deoxycorticosterone level IAGP N RGD:5509061 20141003 MGI PMID:19029289 10428 Cyp11b1 cytochrome P450, family 11, subfamily b, polypeptide 1 gene MP:0014286 increased adrenal gland zona fasciculata size IAGP N RGD:5509061 20230907 MGI PMID:19029289 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210204 MGI PMID:15731365 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:15731365 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15731365 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:18039983 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:15731365 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18039983 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:18039983 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:15731365 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18039983 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:15731365 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:18039983 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18039983 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:18039983 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0004119 hypokalemia IAGP N RGD:5509061 20141003 MGI PMID:18039983 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:18039983 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0005582 increased renin activity IAGP N RGD:5509061 20141003 MGI PMID:15731365 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:18039983 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:15731365 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0008055 increased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:18039983 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15731365 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0008291 abnormal adrenocortical cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15731365 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0008293 abnormal adrenal gland zona glomerulosa morphology IAGP N RGD:5509061 20141003 MGI PMID:15731365 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0008293 abnormal adrenal gland zona glomerulosa morphology IAGP N RGD:5509061 20141003 MGI PMID:24035414 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15731365 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:18039983 10430 Cyp11b2 cytochrome P450, family 11, subfamily b, polypeptide 2 gene MP:0031232 increased circulating angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:15731365 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19047483 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19047483 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17560947 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:17560947 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:14980704 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:17560947 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:17560947 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10623596 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200507 MGI PMID:31147315 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17560947 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19047483 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19047483 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19047483 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:19047483 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19047483 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17560947 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19047483 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0005563 abnormal hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19047483 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19047483 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19047483 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19261855 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15094312 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:19047483 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15094312 10436 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:19047483 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:14980704 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:7761462 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:7761462 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:7761462 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:7761462 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:7761462 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200507 MGI PMID:31147315 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0002271 abnormal pulmonary alveolar duct morphology IAGP N RGD:5509061 20141003 MGI PMID:7761462 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7761462 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15845371 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:7761462 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:7761462 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19261855 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10631128 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15845371 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9772215 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:15094312 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:7761462 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:8643688 10438 Cyp1a2 cytochrome P450, family 1, subfamily a, polypeptide 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7761462 10439 Cyp1b1 cytochrome P450, family 1, subfamily b, polypeptide 1 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:12624268 10439 Cyp1b1 cytochrome P450, family 1, subfamily b, polypeptide 1 gene MP:0004223 hypoplastic trabecular meshwork IAGP N RGD:5509061 20141003 MGI PMID:12624268 10439 Cyp1b1 cytochrome P450, family 1, subfamily b, polypeptide 1 gene MP:0004226 absent Schlemm's canal IAGP N RGD:5509061 20141003 MGI PMID:12624268 10439 Cyp1b1 cytochrome P450, family 1, subfamily b, polypeptide 1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:10051580 10439 Cyp1b1 cytochrome P450, family 1, subfamily b, polypeptide 1 gene MP:0005203 abnormal trabecular meshwork morphology IAGP N RGD:5509061 20141003 MGI PMID:12624268 10439 Cyp1b1 cytochrome P450, family 1, subfamily b, polypeptide 1 gene MP:0005204 abnormal canal of Schlemm morphology IAGP N RGD:5509061 20141003 MGI PMID:12624268 10439 Cyp1b1 cytochrome P450, family 1, subfamily b, polypeptide 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10910056 10439 Cyp1b1 cytochrome P450, family 1, subfamily b, polypeptide 1 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20150430 MGI PMID:12624268 10440 Cyp21a1 cytochrome P450, family 21, subfamily a, polypeptide 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20181227 MGI 10440 Cyp21a1 cytochrome P450, family 21, subfamily a, polypeptide 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 10440 Cyp21a1 cytochrome P450, family 21, subfamily a, polypeptide 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 10440 Cyp21a1 cytochrome P450, family 21, subfamily a, polypeptide 1 gene MP:0003717 pallor IEA N RGD:5509061 20230601 MGI 10440 Cyp21a1 cytochrome P450, family 21, subfamily a, polypeptide 1 gene MP:0009453 enhanced contextual conditioning behavior IEA N RGD:5509061 20210128 MGI 10440 Cyp21a1 cytochrome P450, family 21, subfamily a, polypeptide 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 10440 Cyp21a1 cytochrome P450, family 21, subfamily a, polypeptide 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 10448274 Actre8_m activity response to ethanol 8 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20151204 MGI Created by mouse qtl pipeline PMID:12882366 10448274 Actre8_m activity response to ethanol 8 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20151218 MGI Created by mouse qtl pipeline PMID:12882366|PMID:11529277 10449382 Pas14_m pulmonary adenoma susceptibility 14 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20160212 MGI Created by mouse qtl pipeline PMID:8499946 10449382 Pas14_m pulmonary adenoma susceptibility 14 (mouse) qtl MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20160211 MGI PMID:7813906 10449382 Pas14_m pulmonary adenoma susceptibility 14 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:8499946 10449382 Pas14_m pulmonary adenoma susceptibility 14 (mouse) qtl MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20160211 MGI PMID:14583591 10449382 Pas14_m pulmonary adenoma susceptibility 14 (mouse) qtl MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20160211 MGI PMID:8666392 10449436 Pas17_m pulmonary adenoma susceptibility 17 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20160101 MGI Created by mouse qtl pipeline PMID:8666392 10449436 Pas17_m pulmonary adenoma susceptibility 17 (mouse) qtl MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20160107 MGI PMID:23955086 10449436 Pas17_m pulmonary adenoma susceptibility 17 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20160101 MGI Created by mouse qtl pipeline PMID:8666392 10449436 Pas17_m pulmonary adenoma susceptibility 17 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20160101 MGI Created by mouse qtl pipeline PMID:8666392 10449436 Pas17_m pulmonary adenoma susceptibility 17 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20241101 MGI Created by mouse qtl pipeline PMID:8666392 10449436 Pas17_m pulmonary adenoma susceptibility 17 (mouse) qtl MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20160107 MGI PMID:23955086 10449436 Pas17_m pulmonary adenoma susceptibility 17 (mouse) qtl MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20160107 MGI PMID:8666392 10449437 Pas15_m pulmonary adenoma susceptibility 15 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20160101 MGI Created by mouse qtl pipeline PMID:7894154 10451 Cyp2e1 cytochrome P450, family 2, subfamily e, polypeptide 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17093202 10451 Cyp2e1 cytochrome P450, family 2, subfamily e, polypeptide 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20201231 MGI 10451 Cyp2e1 cytochrome P450, family 2, subfamily e, polypeptide 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:10772651 10451 Cyp2e1 cytochrome P450, family 2, subfamily e, polypeptide 1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17093202 10451 Cyp2e1 cytochrome P450, family 2, subfamily e, polypeptide 1 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:17093202 10451 Cyp2e1 cytochrome P450, family 2, subfamily e, polypeptide 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18990727 10451 Cyp2e1 cytochrome P450, family 2, subfamily e, polypeptide 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:8662637 10451 Cyp2e1 cytochrome P450, family 2, subfamily e, polypeptide 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9772215 10451 Cyp2e1 cytochrome P450, family 2, subfamily e, polypeptide 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:18990727 10451 Cyp2e1 cytochrome P450, family 2, subfamily e, polypeptide 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18990727 10451 Cyp2e1 cytochrome P450, family 2, subfamily e, polypeptide 1 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18990727 10451 Cyp2e1 cytochrome P450, family 2, subfamily e, polypeptide 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18990727 10451 Cyp2e1 cytochrome P450, family 2, subfamily e, polypeptide 1 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:8662637 10452 Cyp2g1 cytochrome P450, family 2, subfamily g, polypeptide 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20147558 10452 Cyp2g1 cytochrome P450, family 2, subfamily g, polypeptide 1 gene MP:0001867 rhinitis IAGP N RGD:5509061 20141003 MGI PMID:20147558 10452 Cyp2g1 cytochrome P450, family 2, subfamily g, polypeptide 1 gene MP:0004512 anosmia IAGP N RGD:5509061 20141003 MGI PMID:20147558 10452 Cyp2g1 cytochrome P450, family 2, subfamily g, polypeptide 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:14610229 10452 Cyp2g1 cytochrome P450, family 2, subfamily g, polypeptide 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:20147558 10452 Cyp2g1 cytochrome P450, family 2, subfamily g, polypeptide 1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20147558 10452 Cyp2g1 cytochrome P450, family 2, subfamily g, polypeptide 1 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:20147558 10452 Cyp2g1 cytochrome P450, family 2, subfamily g, polypeptide 1 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20147558 10457 Cyp4b1 cytochrome P450, family 4, subfamily b, polypeptide 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 10457 Cyp4b1 cytochrome P450, family 4, subfamily b, polypeptide 1 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20170105 MGI 10457 Cyp4b1 cytochrome P450, family 4, subfamily b, polypeptide 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 10457 Cyp4b1 cytochrome P450, family 4, subfamily b, polypeptide 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 10457 Cyp4b1 cytochrome P450, family 4, subfamily b, polypeptide 1 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20170105 MGI 10457 Cyp4b1 cytochrome P450, family 4, subfamily b, polypeptide 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23748241 10457 Cyp4b1 cytochrome P450, family 4, subfamily b, polypeptide 1 gene MP:0010511 shortened PR interval IEA N RGD:5509061 20210128 MGI 10457 Cyp4b1 cytochrome P450, family 4, subfamily b, polypeptide 1 gene MP:0011954 shortened PQ interval IEA N RGD:5509061 20210128 MGI 10457 Cyp4b1 cytochrome P450, family 4, subfamily b, polypeptide 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001197 oily skin IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001238 thin epidermis stratum spinosum IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20181227 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8663430 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:11368757 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0002791 steatorrhea IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0003849 greasy coat IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20210128 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:8663430 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:8663430 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0005401 abnormal fat-soluble vitamin level IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0005401 abnormal fat-soluble vitamin level IAGP N RGD:5509061 20141003 MGI PMID:8663430 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20201022 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8663429 10458 Cyp7a1 cytochrome P450, family 7, subfamily a, polypeptide 1 gene MP:0011896 increased circulating unsaturated transferrin level IEA N RGD:5509061 20181227 MGI 10459 Cyp7b1 cytochrome P450, family 7, subfamily b, polypeptide 1 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:15710898 10459 Cyp7b1 cytochrome P450, family 7, subfamily b, polypeptide 1 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:19805370 10459 Cyp7b1 cytochrome P450, family 7, subfamily b, polypeptide 1 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:15710898 10459 Cyp7b1 cytochrome P450, family 7, subfamily b, polypeptide 1 gene MP:0003378 early sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:15710898 10459 Cyp7b1 cytochrome P450, family 7, subfamily b, polypeptide 1 gene MP:0003572 abnormal uterus development IAGP N RGD:5509061 20141003 MGI PMID:15710898 10459 Cyp7b1 cytochrome P450, family 7, subfamily b, polypeptide 1 gene MP:0004894 uterus atrophy IAGP N RGD:5509061 20141003 MGI PMID:15710898 10459 Cyp7b1 cytochrome P450, family 7, subfamily b, polypeptide 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10748047 10459 Cyp7b1 cytochrome P450, family 7, subfamily b, polypeptide 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10748048 10459 Cyp7b1 cytochrome P450, family 7, subfamily b, polypeptide 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 10459 Cyp7b1 cytochrome P450, family 7, subfamily b, polypeptide 1 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:15710898 10459 Cyp7b1 cytochrome P450, family 7, subfamily b, polypeptide 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 10459 Cyp7b1 cytochrome P450, family 7, subfamily b, polypeptide 1 gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20200227 MGI PMID:15710898 10460 Dbh dopamine beta hydroxylase gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:7715704 10460 Dbh dopamine beta hydroxylase gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16723393 10460 Dbh dopamine beta hydroxylase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16723393 10460 Dbh dopamine beta hydroxylase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7715704 10460 Dbh dopamine beta hydroxylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:7715704 10460 Dbh dopamine beta hydroxylase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10518589 10460 Dbh dopamine beta hydroxylase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16723393 10460 Dbh dopamine beta hydroxylase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10518589 10460 Dbh dopamine beta hydroxylase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16723393 10460 Dbh dopamine beta hydroxylase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10518589 10460 Dbh dopamine beta hydroxylase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16723393 10460 Dbh dopamine beta hydroxylase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10518589 10460 Dbh dopamine beta hydroxylase gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:10518589 10460 Dbh dopamine beta hydroxylase gene MP:0001428 adipsia IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:16723393 10460 Dbh dopamine beta hydroxylase gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:16723393 10460 Dbh dopamine beta hydroxylase gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0001443 poor grooming IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0001462 abnormal avoidance learning behavior IAGP N RGD:5509061 20141003 MGI PMID:19864633 10460 Dbh dopamine beta hydroxylase gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:10518589 10460 Dbh dopamine beta hydroxylase gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:16723393 10460 Dbh dopamine beta hydroxylase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7715704 10460 Dbh dopamine beta hydroxylase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0001742 absent circulating adrenaline IAGP N RGD:5509061 20141003 MGI PMID:7715704 10460 Dbh dopamine beta hydroxylase gene MP:0001743 absent circulating noradrenaline IAGP N RGD:5509061 20141003 MGI PMID:7715704 10460 Dbh dopamine beta hydroxylase gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:12959968 10460 Dbh dopamine beta hydroxylase gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15724149 10460 Dbh dopamine beta hydroxylase gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:7715704 10460 Dbh dopamine beta hydroxylase gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:16723393 10460 Dbh dopamine beta hydroxylase gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12959968 10460 Dbh dopamine beta hydroxylase gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12959968 10460 Dbh dopamine beta hydroxylase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10518589 10460 Dbh dopamine beta hydroxylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16723393 10460 Dbh dopamine beta hydroxylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7715704 10460 Dbh dopamine beta hydroxylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23852112 10460 Dbh dopamine beta hydroxylase gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:10518589 10460 Dbh dopamine beta hydroxylase gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:12959968 10460 Dbh dopamine beta hydroxylase gene MP:0002711 decreased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:12959968 10460 Dbh dopamine beta hydroxylase gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:16723393 10460 Dbh dopamine beta hydroxylase gene MP:0002822 catalepsy IAGP N RGD:5509061 20141003 MGI PMID:10518589 10460 Dbh dopamine beta hydroxylase gene MP:0003063 increased coping response IAGP N RGD:5509061 20200402 MGI PMID:32065256 10460 Dbh dopamine beta hydroxylase gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0003908 decreased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:23684624 10460 Dbh dopamine beta hydroxylase gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:16723393 10460 Dbh dopamine beta hydroxylase gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12959968 10460 Dbh dopamine beta hydroxylase gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:12959968 10460 Dbh dopamine beta hydroxylase gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:10518589 10460 Dbh dopamine beta hydroxylase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12959968 10460 Dbh dopamine beta hydroxylase gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:23684624 10460 Dbh dopamine beta hydroxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:16723393 10460 Dbh dopamine beta hydroxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:19864633 10460 Dbh dopamine beta hydroxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:23852112 10460 Dbh dopamine beta hydroxylase gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:10518589 10460 Dbh dopamine beta hydroxylase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7715704 10460 Dbh dopamine beta hydroxylase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23852112 10460 Dbh dopamine beta hydroxylase gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7715704 10460 Dbh dopamine beta hydroxylase gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8548806 10460 Dbh dopamine beta hydroxylase gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20200402 MGI PMID:32065256 10460 Dbh dopamine beta hydroxylase gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:16723393 10460 Dbh dopamine beta hydroxylase gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:10518589 10460 Dbh dopamine beta hydroxylase gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:10518589 10460 Dbh dopamine beta hydroxylase gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:16723393 10460 Dbh dopamine beta hydroxylase gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:23684624 10463 Dbi diazepam binding inhibitor gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:21106527 10463 Dbi diazepam binding inhibitor gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:24316079 10463 Dbi diazepam binding inhibitor gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:21106527 10463 Dbi diazepam binding inhibitor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21106527 10463 Dbi diazepam binding inhibitor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21106527 10463 Dbi diazepam binding inhibitor gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:21106527 10463 Dbi diazepam binding inhibitor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24316079 10463 Dbi diazepam binding inhibitor gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:24316079 10463 Dbi diazepam binding inhibitor gene MP:0003849 greasy coat IAGP N RGD:5509061 20141003 MGI PMID:24316079 10463 Dbi diazepam binding inhibitor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21106527 10463 Dbi diazepam binding inhibitor gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21106527 10463 Dbi diazepam binding inhibitor gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:24316079 10463 Dbi diazepam binding inhibitor gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21106527 10463 Dbi diazepam binding inhibitor gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:24316079 10463 Dbi diazepam binding inhibitor gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21106527 10463 Dbi diazepam binding inhibitor gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:24316079 10463 Dbi diazepam binding inhibitor gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21106527 10463 Dbi diazepam binding inhibitor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20559753 10464 Dbp D site albumin promoter binding protein gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180705 MGI PMID:16814730 10464 Dbp D site albumin promoter binding protein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9362490 10464 Dbp D site albumin promoter binding protein gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:15175240 10464 Dbp D site albumin promoter binding protein gene MP:0001596 hypotension IAGP N RGD:5509061 20180705 MGI PMID:20686175 10464 Dbp D site albumin promoter binding protein gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20180705 MGI PMID:20686175 10464 Dbp D site albumin promoter binding protein gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15175240 10464 Dbp D site albumin promoter binding protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15175240 10464 Dbp D site albumin promoter binding protein gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15175240 10464 Dbp D site albumin promoter binding protein gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20180705 MGI PMID:20686175 10464 Dbp D site albumin promoter binding protein gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180705 MGI PMID:16814730 10464 Dbp D site albumin promoter binding protein gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:15175240 10464 Dbp D site albumin promoter binding protein gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:15175240 10464 Dbp D site albumin promoter binding protein gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:15175240 10464 Dbp D site albumin promoter binding protein gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20180920 MGI PMID:15175240 10464 Dbp D site albumin promoter binding protein gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180705 MGI PMID:16814730 10464 Dbp D site albumin promoter binding protein gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20180705 MGI PMID:16814730 10464 Dbp D site albumin promoter binding protein gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:15175240 10464 Dbp D site albumin promoter binding protein gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:9362490 10464 Dbp D site albumin promoter binding protein gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20171012 MGI PMID:9362490 10465 Dcc DCC netrin 1 receptor gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 10465 Dcc DCC netrin 1 receptor gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22158121 10465 Dcc DCC netrin 1 receptor gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22358843 10465 Dcc DCC netrin 1 receptor gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9331350 10465 Dcc DCC netrin 1 receptor gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:9331350 10465 Dcc DCC netrin 1 receptor gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12451134 10465 Dcc DCC netrin 1 receptor gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12451134 10465 Dcc DCC netrin 1 receptor gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9126737 10465 Dcc DCC netrin 1 receptor gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22358843 10465 Dcc DCC netrin 1 receptor gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9126737 10465 Dcc DCC netrin 1 receptor gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22358843 10465 Dcc DCC netrin 1 receptor gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:22358843 10465 Dcc DCC netrin 1 receptor gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:12451134 10465 Dcc DCC netrin 1 receptor gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:22358843 10465 Dcc DCC netrin 1 receptor gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:9126737 10465 Dcc DCC netrin 1 receptor gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22158121 10465 Dcc DCC netrin 1 receptor gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9126737 10465 Dcc DCC netrin 1 receptor gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:12451134 10465 Dcc DCC netrin 1 receptor gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22158121 10465 Dcc DCC netrin 1 receptor gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:12451134 10465 Dcc DCC netrin 1 receptor gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:9126737 10465 Dcc DCC netrin 1 receptor gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9331350 10465 Dcc DCC netrin 1 receptor gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22358843 10465 Dcc DCC netrin 1 receptor gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:12451134 10465 Dcc DCC netrin 1 receptor gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:9126737 10465 Dcc DCC netrin 1 receptor gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:9126737 10465 Dcc DCC netrin 1 receptor gene MP:0009681 abnormal pyramidal decussation morphology IAGP N RGD:5509061 20141003 MGI PMID:12451134 10465 Dcc DCC netrin 1 receptor gene MP:0010273 increased classified tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22358843 10465 Dcc DCC netrin 1 receptor gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22158121 10465 Dcc DCC netrin 1 receptor gene MP:0010307 abnormal tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22358843 10465 Dcc DCC netrin 1 receptor gene MP:0010367 increased spindle cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22358843 10465 Dcc DCC netrin 1 receptor gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22358843 10465 Dcc DCC netrin 1 receptor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9126737 10465 Dcc DCC netrin 1 receptor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170105 MGI 10465 Dcc DCC netrin 1 receptor gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20160317 MGI PMID:26858598 10465 Dcc DCC netrin 1 receptor gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:22158121 10465 Dcc DCC netrin 1 receptor gene MP:0014234 decreased enterocyte apoptosis IAGP N RGD:5509061 20230323 MGI PMID:22158121 10465 Dcc DCC netrin 1 receptor gene MP:0020399 enhanced megakaryocyte emperipolesis IAGP N RGD:5509061 20170803 MGI PMID:18033315 10465 Dcc DCC netrin 1 receptor gene MP:0020560 abnormal pontine nuclei morphology IAGP N RGD:5509061 20180315 MGI PMID:12451134 10465 Dcc DCC netrin 1 receptor gene MP:0020560 abnormal pontine nuclei morphology IAGP N RGD:5509061 20180315 MGI PMID:9126737 10468 Ace angiotensin I converting enzyme gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12637363 10468 Ace angiotensin I converting enzyme gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18158355 10468 Ace angiotensin I converting enzyme gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21115616 10468 Ace angiotensin I converting enzyme gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:9482924 10468 Ace angiotensin I converting enzyme gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9039095 10468 Ace angiotensin I converting enzyme gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12637363 10468 Ace angiotensin I converting enzyme gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:7753170 10468 Ace angiotensin I converting enzyme gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:8598926 10468 Ace angiotensin I converting enzyme gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9482924 10468 Ace angiotensin I converting enzyme gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15522949 10468 Ace angiotensin I converting enzyme gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15522949 10468 Ace angiotensin I converting enzyme gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 10468 Ace angiotensin I converting enzyme gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:18158355 10468 Ace angiotensin I converting enzyme gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:12075344 10468 Ace angiotensin I converting enzyme gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:7753170 10468 Ace angiotensin I converting enzyme gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221103 MGI 10468 Ace angiotensin I converting enzyme gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:21115616 10468 Ace angiotensin I converting enzyme gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:9153279 10468 Ace angiotensin I converting enzyme gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18158355 10468 Ace angiotensin I converting enzyme gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:21115616 10468 Ace angiotensin I converting enzyme gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:7753170 10468 Ace angiotensin I converting enzyme gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:8598926 10468 Ace angiotensin I converting enzyme gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20141003 MGI PMID:12637363 10468 Ace angiotensin I converting enzyme gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:7753170 10468 Ace angiotensin I converting enzyme gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:9153279 10468 Ace angiotensin I converting enzyme gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:7753170 10468 Ace angiotensin I converting enzyme gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9153279 10468 Ace angiotensin I converting enzyme gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15331425 10468 Ace angiotensin I converting enzyme gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12075344 10468 Ace angiotensin I converting enzyme gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12637363 10468 Ace angiotensin I converting enzyme gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:18158355 10468 Ace angiotensin I converting enzyme gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20231207 MGI 10468 Ace angiotensin I converting enzyme gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:9039095 10468 Ace angiotensin I converting enzyme gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:9039095 10468 Ace angiotensin I converting enzyme gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:9039095 10468 Ace angiotensin I converting enzyme gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11687636 10468 Ace angiotensin I converting enzyme gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:11687636 10468 Ace angiotensin I converting enzyme gene MP:0002987 abnormal urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:21115616 10468 Ace angiotensin I converting enzyme gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:12637363 10468 Ace angiotensin I converting enzyme gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:18158355 10468 Ace angiotensin I converting enzyme gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:21115616 10468 Ace angiotensin I converting enzyme gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:8598926 10468 Ace angiotensin I converting enzyme gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:9153279 10468 Ace angiotensin I converting enzyme gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:21115616 10468 Ace angiotensin I converting enzyme gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:8598926 10468 Ace angiotensin I converting enzyme gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15522949 10468 Ace angiotensin I converting enzyme gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15522949 10468 Ace angiotensin I converting enzyme gene MP:0003184 increased angiotensin I-converting enzyme activity IAGP N RGD:5509061 20141003 MGI PMID:20651228 10468 Ace angiotensin I converting enzyme gene MP:0003185 decreased angiotensin I-converting enzyme activity IAGP N RGD:5509061 20141003 MGI PMID:18158355 10468 Ace angiotensin I converting enzyme gene MP:0003185 decreased angiotensin I-converting enzyme activity IAGP N RGD:5509061 20141003 MGI PMID:20651228 10468 Ace angiotensin I converting enzyme gene MP:0003185 decreased angiotensin I-converting enzyme activity IAGP N RGD:5509061 20141003 MGI PMID:21115616 10468 Ace angiotensin I converting enzyme gene MP:0003185 decreased angiotensin I-converting enzyme activity IAGP N RGD:5509061 20210204 MGI PMID:14757757 10468 Ace angiotensin I converting enzyme gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:14757757 10468 Ace angiotensin I converting enzyme gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:17525278 10468 Ace angiotensin I converting enzyme gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:17525278 10468 Ace angiotensin I converting enzyme gene MP:0003626 kidney medulla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12637363 10468 Ace angiotensin I converting enzyme gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:12637363 10468 Ace angiotensin I converting enzyme gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18158355 10468 Ace angiotensin I converting enzyme gene MP:0003670 dilated renal glomerular capsule IAGP N RGD:5509061 20141003 MGI PMID:8598926 10468 Ace angiotensin I converting enzyme gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12637363 10468 Ace angiotensin I converting enzyme gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:12637363 10468 Ace angiotensin I converting enzyme gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20221103 MGI 10468 Ace angiotensin I converting enzyme gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20141003 MGI PMID:12637363 10468 Ace angiotensin I converting enzyme gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20141003 MGI PMID:21115616 10468 Ace angiotensin I converting enzyme gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20141003 MGI PMID:8598926 10468 Ace angiotensin I converting enzyme gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:15331425 10468 Ace angiotensin I converting enzyme gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:9482924 10468 Ace angiotensin I converting enzyme gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17525278 10468 Ace angiotensin I converting enzyme gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:20651228 10468 Ace angiotensin I converting enzyme gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20200416 MGI PMID:16001071 10468 Ace angiotensin I converting enzyme gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:7753170 10468 Ace angiotensin I converting enzyme gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:9039095 10468 Ace angiotensin I converting enzyme gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:9039095 10468 Ace angiotensin I converting enzyme gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:18158355 10468 Ace angiotensin I converting enzyme gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:8598926 10468 Ace angiotensin I converting enzyme gene MP:0005582 increased renin activity IAGP N RGD:5509061 20141003 MGI PMID:18158355 10468 Ace angiotensin I converting enzyme gene MP:0005582 increased renin activity IAGP N RGD:5509061 20141003 MGI PMID:21115616 10468 Ace angiotensin I converting enzyme gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12637363 10468 Ace angiotensin I converting enzyme gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15331425 10468 Ace angiotensin I converting enzyme gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21115616 10468 Ace angiotensin I converting enzyme gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9153279 10468 Ace angiotensin I converting enzyme gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15522949 10468 Ace angiotensin I converting enzyme gene MP:0006373 abnormal circulating angiotensinogen level IAGP N RGD:5509061 20141003 MGI PMID:21115616 10468 Ace angiotensin I converting enzyme gene MP:0006376 decreased circulating angiotensinogen level IAGP N RGD:5509061 20141003 MGI PMID:21115616 10468 Ace angiotensin I converting enzyme gene MP:0008543 atrial fibrillation IAGP N RGD:5509061 20141003 MGI PMID:15331425 10468 Ace angiotensin I converting enzyme gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:15331425 10468 Ace angiotensin I converting enzyme gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:17525278 10468 Ace angiotensin I converting enzyme gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:15331425 10468 Ace angiotensin I converting enzyme gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20191017 MGI PMID:9482924 10468 Ace angiotensin I converting enzyme gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20651228 10468 Ace angiotensin I converting enzyme gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7753170 10468 Ace angiotensin I converting enzyme gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8598926 10468 Ace angiotensin I converting enzyme gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9482924 10468 Ace angiotensin I converting enzyme gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210422 MGI 10468 Ace angiotensin I converting enzyme gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20191017 MGI PMID:7753170 10468 Ace angiotensin I converting enzyme gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0011305 dilated kidney calyx IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0011305 dilated kidney calyx IAGP N RGD:5509061 20141003 MGI PMID:9153279 10468 Ace angiotensin I converting enzyme gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20141003 MGI PMID:8598926 10468 Ace angiotensin I converting enzyme gene MP:0011309 abnormal kidney arterial blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0011309 abnormal kidney arterial blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:9153279 10468 Ace angiotensin I converting enzyme gene MP:0011317 abnormal renal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21115616 10468 Ace angiotensin I converting enzyme gene MP:0011317 abnormal renal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:7753170 10468 Ace angiotensin I converting enzyme gene MP:0011347 abnormal kidney medullary ray morphology IAGP N RGD:5509061 20141003 MGI PMID:8598926 10468 Ace angiotensin I converting enzyme gene MP:0011376 abnormal kidney corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:8598926 10468 Ace angiotensin I converting enzyme gene MP:0011422 kidney medulla atrophy IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20141003 MGI PMID:7753170 10468 Ace angiotensin I converting enzyme gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20141003 MGI PMID:8598926 10468 Ace angiotensin I converting enzyme gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:9153279 10468 Ace angiotensin I converting enzyme gene MP:0011541 decreased urine aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:8642790 10468 Ace angiotensin I converting enzyme gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:15522949 10468 Ace angiotensin I converting enzyme gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:21115616 10468 Ace angiotensin I converting enzyme gene MP:0013254 abnormal angiotensin I-converting enzyme activity IAGP N RGD:5509061 20210204 MGI PMID:18158355 10468 Ace angiotensin I converting enzyme gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191017 MGI PMID:9482924 10468 Ace angiotensin I converting enzyme gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220303 MGI PMID:9482924 10468 Ace angiotensin I converting enzyme gene MP:0031228 decreased angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:16001071 10468 Ace angiotensin I converting enzyme gene MP:0031231 decreased circulating angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:16001071 10468 Ace angiotensin I converting enzyme gene MP:0031231 decreased circulating angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:18158355 10469 Ddc dopa decarboxylase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20180726 MGI PMID:28973165 10469 Ddc dopa decarboxylase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180726 MGI PMID:28973165 10469 Ddc dopa decarboxylase gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20180726 MGI PMID:28973165 10469 Ddc dopa decarboxylase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180726 MGI PMID:28973165 10469 Ddc dopa decarboxylase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20180726 MGI PMID:28973165 10469 Ddc dopa decarboxylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21701066 10469 Ddc dopa decarboxylase gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20180726 MGI PMID:28973165 10469 Ddc dopa decarboxylase gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20200514 MGI 10469 Ddc dopa decarboxylase gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:21701066 10469 Ddc dopa decarboxylase gene MP:0002204 abnormal synaptic neurotransmitter level IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 10469 Ddc dopa decarboxylase gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:21701066 10469 Ddc dopa decarboxylase gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21701066 10469 Ddc dopa decarboxylase gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:21701066 10469 Ddc dopa decarboxylase gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:21701066 10469 Ddc dopa decarboxylase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:21701066 10469 Ddc dopa decarboxylase gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:21701066 10469 Ddc dopa decarboxylase gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20141003 MGI PMID:21701066 10469 Ddc dopa decarboxylase gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21701066 10469 Ddc dopa decarboxylase gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:21701066 10469 Ddc dopa decarboxylase gene MP:0005582 increased renin activity IAGP N RGD:5509061 20141003 MGI PMID:21701066 10469 Ddc dopa decarboxylase gene MP:0005583 decreased renin activity IAGP N RGD:5509061 20141003 MGI PMID:21701066 10469 Ddc dopa decarboxylase gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20240523 MGI 10469 Ddc dopa decarboxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:21701066 10469 Ddc dopa decarboxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20180726 MGI PMID:28973165 10469 Ddc dopa decarboxylase gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21701066 10469 Ddc dopa decarboxylase gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180726 MGI PMID:28973165 10469 Ddc dopa decarboxylase gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180726 MGI PMID:28973165 10469 Ddc dopa decarboxylase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180726 MGI PMID:28973165 10469 Ddc dopa decarboxylase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 10469 Ddc dopa decarboxylase gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23275025 10469 Ddc dopa decarboxylase gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20180726 MGI PMID:28973165 10469 Ddc dopa decarboxylase gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:21701066 10470 Ddx6 DEAD-box helicase 6 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 10470 Ddx6 DEAD-box helicase 6 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20230928 MGI PMID:31657143 10470 Ddx6 DEAD-box helicase 6 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20230928 MGI PMID:31657143 10470 Ddx6 DEAD-box helicase 6 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20190502 MGI 10470 Ddx6 DEAD-box helicase 6 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20230126 MGI PMID:36197846 10470 Ddx6 DEAD-box helicase 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20230126 MGI PMID:36197846 10470 Ddx6 DEAD-box helicase 6 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20220811 MGI 10470 Ddx6 DEAD-box helicase 6 gene MP:0001926 female infertility IAGP N RGD:5509061 20230928 MGI PMID:31657143 10470 Ddx6 DEAD-box helicase 6 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 10470 Ddx6 DEAD-box helicase 6 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 10470 Ddx6 DEAD-box helicase 6 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20220811 MGI 10470 Ddx6 DEAD-box helicase 6 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20230126 MGI PMID:36197846 10470 Ddx6 DEAD-box helicase 6 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 10470 Ddx6 DEAD-box helicase 6 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20230126 MGI PMID:36197846 10470 Ddx6 DEAD-box helicase 6 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20230126 MGI PMID:36197846 10470 Ddx6 DEAD-box helicase 6 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20230928 MGI PMID:31657143 10470 Ddx6 DEAD-box helicase 6 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20230126 MGI PMID:36197846 10470 Ddx6 DEAD-box helicase 6 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 10470 Ddx6 DEAD-box helicase 6 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20221215 MGI 10470 Ddx6 DEAD-box helicase 6 gene MP:0009361 abnormal primordial ovarian follicle morphology IAGP N RGD:5509061 20230928 MGI PMID:31657143 10470 Ddx6 DEAD-box helicase 6 gene MP:0009850 embryonic lethality between implantation and placentation IAGP N RGD:5509061 20230126 MGI PMID:36197846 10470 Ddx6 DEAD-box helicase 6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20230126 MGI PMID:36197846 10470 Ddx6 DEAD-box helicase 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10470 Ddx6 DEAD-box helicase 6 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20230928 MGI PMID:31657143 10470 Ddx6 DEAD-box helicase 6 gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20230928 MGI PMID:31657143 10470 Ddx6 DEAD-box helicase 6 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20230928 MGI PMID:31657143 10470 Ddx6 DEAD-box helicase 6 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 10470 Ddx6 DEAD-box helicase 6 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 10470 Ddx6 DEAD-box helicase 6 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20230928 MGI PMID:31657143 10471 Dhfr dihydrofolate reductase gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0000603 pale liver IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0003717 pallor IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20181227 MGI 10471 Dhfr dihydrofolate reductase gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 10471 Dhfr dihydrofolate reductase gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20180719 MGI 10471 Dhfr dihydrofolate reductase gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0011230 abnormal folic acid level IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 10471 Dhfr dihydrofolate reductase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 10471 Dhfr dihydrofolate reductase gene MP:0013693 abnormal hemopoiesis IAGP N RGD:5509061 20180719 MGI PMID:26830229 10471 Dhfr dihydrofolate reductase gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20180719 MGI PMID:26830229 10473 Nqo1 NAD(P)H dehydrogenase, quinone 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11309386 10473 Nqo1 NAD(P)H dehydrogenase, quinone 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11309386 10473 Nqo1 NAD(P)H dehydrogenase, quinone 1 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:11309386 10473 Nqo1 NAD(P)H dehydrogenase, quinone 1 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20141003 MGI PMID:11309386 10473 Nqo1 NAD(P)H dehydrogenase, quinone 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:11309386 10473 Nqo1 NAD(P)H dehydrogenase, quinone 1 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:11309386 10473 Nqo1 NAD(P)H dehydrogenase, quinone 1 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11309386 10473 Nqo1 NAD(P)H dehydrogenase, quinone 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11309386 10473 Nqo1 NAD(P)H dehydrogenase, quinone 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11309386 10473 Nqo1 NAD(P)H dehydrogenase, quinone 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:9516435 10473 Nqo1 NAD(P)H dehydrogenase, quinone 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19136651 10473 Nqo1 NAD(P)H dehydrogenase, quinone 1 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11309386 10473 Nqo1 NAD(P)H dehydrogenase, quinone 1 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11085502 10474 Dio1 deiodinase, iodothyronine, type I gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16223863 10474 Dio1 deiodinase, iodothyronine, type I gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 10474 Dio1 deiodinase, iodothyronine, type I gene MP:0002876 abnormal thyroid gland physiology IAGP N RGD:5509061 20141003 MGI PMID:16223863 10474 Dio1 deiodinase, iodothyronine, type I gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:16223863 10474 Dio1 deiodinase, iodothyronine, type I gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:16223863 10474 Dio1 deiodinase, iodothyronine, type I gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16223863 10474 Dio1 deiodinase, iodothyronine, type I gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:16223863 10474 Dio1 deiodinase, iodothyronine, type I gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:16223863 10474 Dio1 deiodinase, iodothyronine, type I gene MP:0005474 increased triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:16223863 10474 Dio1 deiodinase, iodothyronine, type I gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:16223863 10474 Dio1 deiodinase, iodothyronine, type I gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:16223863 10474 Dio1 deiodinase, iodothyronine, type I gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16223863 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:18842882 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19623611 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:11238884 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:11238884 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11238884 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19139088 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:16105026 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:11238884 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11238884 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:11238884 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:19623611 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:19623611 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11238884 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18842882 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19623611 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0002990 short ureter IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:23028902 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:11238884 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14645510 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19623611 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003535 absent vagina IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003584 bifid ureter IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003585 large ureter IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003586 dilated ureter IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003826 abnormal Mullerian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0003847 disorganized lens bow IAGP N RGD:5509061 20141003 MGI PMID:19623611 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:16105026 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11238884 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:16105026 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11238884 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23028902 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:23028902 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:23028902 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:19623611 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18842882 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23028902 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23028902 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:23028902 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:23028902 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:23028902 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0008794 increased lens epithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19623611 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0008796 increased lens fiber apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19623611 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0009084 blind uterus IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:11238884 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:16105026 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:11238884 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:11238884 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:11238884 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141003 MGI PMID:24048858 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11238884 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23028902 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:16105026 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0011298 ureter hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0011365 small metanephros IAGP N RGD:5509061 20141003 MGI PMID:16105026 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0011426 abnormal ureter smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0011480 impaired ureteric peristalsis IAGP N RGD:5509061 20141003 MGI PMID:17172448 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0011484 abnormal ureter urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17435047 10475 Dlg1 discs large MAGUK scaffold protein 1 gene MP:0011727 ectopic ovary IAGP N RGD:5509061 20141003 MGI PMID:17435047 10476 Dlx5 distal-less homeobox 5 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:12142028 10476 Dlx5 distal-less homeobox 5 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:12142028 10476 Dlx5 distal-less homeobox 5 gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0000041 absent endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0000084 abnormal fontanelle morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20171207 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0000094 absent alveolar process IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0000098 abnormal vomer bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20171214 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12112878 10476 Dlx5 distal-less homeobox 5 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:12112878 10476 Dlx5 distal-less homeobox 5 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:18326838 10476 Dlx5 distal-less homeobox 5 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:12533617 10476 Dlx5 distal-less homeobox 5 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:12112878 10476 Dlx5 distal-less homeobox 5 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0002238 abnormal nasal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0002249 abnormal larynx morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:12142028 10476 Dlx5 distal-less homeobox 5 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:12112878 10476 Dlx5 distal-less homeobox 5 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:12533617 10476 Dlx5 distal-less homeobox 5 gene MP:0002817 abnormal tooth mineralization IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12112878 10476 Dlx5 distal-less homeobox 5 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:12142028 10476 Dlx5 distal-less homeobox 5 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:12142028 10476 Dlx5 distal-less homeobox 5 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0003165 absent superior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0003165 absent superior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0003168 abnormal scala vestibuli morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12533617 10476 Dlx5 distal-less homeobox 5 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0003800 monodactyly IAGP N RGD:5509061 20141003 MGI PMID:18326838 10476 Dlx5 distal-less homeobox 5 gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0003931 absent molars IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0003932 abnormal molar crown morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:12112878 10476 Dlx5 distal-less homeobox 5 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:12533617 10476 Dlx5 distal-less homeobox 5 gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0004237 abnormal pterygoid muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:12142028 10476 Dlx5 distal-less homeobox 5 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:12533617 10476 Dlx5 distal-less homeobox 5 gene MP:0004311 otic vesicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12142028 10476 Dlx5 distal-less homeobox 5 gene MP:0004330 abnormal vestibular saccular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:12142028 10476 Dlx5 distal-less homeobox 5 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:12142028 10476 Dlx5 distal-less homeobox 5 gene MP:0004335 enlarged utricle IAGP N RGD:5509061 20141003 MGI PMID:12142028 10476 Dlx5 distal-less homeobox 5 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0004409 abnormal crista ampullaris neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0004444 small supraoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0004477 turbinate hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0004540 small maxilla IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0004594 abnormal mandibular coronoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0004594 abnormal mandibular coronoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0004595 abnormal mandibular condyloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0004595 abnormal mandibular condyloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0004665 abnormal stapedial artery morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0005230 ectrodactyly IAGP N RGD:5509061 20141003 MGI PMID:12112878 10476 Dlx5 distal-less homeobox 5 gene MP:0005230 ectrodactyly IAGP N RGD:5509061 20141003 MGI PMID:18326838 10476 Dlx5 distal-less homeobox 5 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12533617 10476 Dlx5 distal-less homeobox 5 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0005271 abnormal lacrimal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:12112878 10476 Dlx5 distal-less homeobox 5 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:18326838 10476 Dlx5 distal-less homeobox 5 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0006033 abnormal external auditory canal morphology IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:12142028 10476 Dlx5 distal-less homeobox 5 gene MP:0006289 otic capsule hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0006306 abnormal nasal pit morphology IAGP N RGD:5509061 20141003 MGI PMID:12533617 10476 Dlx5 distal-less homeobox 5 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:12112878 10476 Dlx5 distal-less homeobox 5 gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0008065 short endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:12142028 10476 Dlx5 distal-less homeobox 5 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0008378 small malleus processus brevis IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0008379 absent malleus head IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0008380 abnormal gonial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12533617 10476 Dlx5 distal-less homeobox 5 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0009893 cleft primary palate IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0009897 decreased maxillary shelf size IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:12533617 10476 Dlx5 distal-less homeobox 5 gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20171026 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0009913 abnormal hyoid bone greater horn morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0009918 abnormal stylohyoid ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0009942 abnormal olfactory bulb granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12533617 10476 Dlx5 distal-less homeobox 5 gene MP:0009943 abnormal olfactory bulb periglomerular cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12533617 10476 Dlx5 distal-less homeobox 5 gene MP:0009954 abnormal mitral cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12533617 10476 Dlx5 distal-less homeobox 5 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0010939 abnormal mandibular prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16330189 10476 Dlx5 distal-less homeobox 5 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12112878 10476 Dlx5 distal-less homeobox 5 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20240627 MGI PMID:12533617 10476 Dlx5 distal-less homeobox 5 gene MP:0012176 abnormal head development IAGP N RGD:5509061 20141003 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0013595 absent vomeronasal organ IAGP N RGD:5509061 20150319 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0013597 small vomeronasal organ IAGP N RGD:5509061 20150319 MGI PMID:12533617 10476 Dlx5 distal-less homeobox 5 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0014155 absent olfactory epithelium IAGP N RGD:5509061 20160407 MGI PMID:12533617 10476 Dlx5 distal-less homeobox 5 gene MP:0014166 ectopic cranial bone IAGP N RGD:5509061 20160407 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0014166 ectopic cranial bone IAGP N RGD:5509061 20160407 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0020350 fused pharyngeal arches IAGP N RGD:5509061 20160915 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0030030 Wormian bones IAGP N RGD:5509061 20170810 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0030055 small lacrimal bone IAGP N RGD:5509061 20170921 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0030089 short lower incisors IAGP N RGD:5509061 20170928 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0030090 short upper incisors IAGP N RGD:5509061 20170928 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0030148 abnormal mylohyoid muscle morphology IAGP N RGD:5509061 20171005 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0030187 abnormal epitympanic recess morphology IAGP N RGD:5509061 20171012 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0030199 deviated nasal septum IAGP N RGD:5509061 20171012 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0030203 short nasal septum IAGP N RGD:5509061 20171012 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0030208 abnormal intrinsic tongue muscle morphology IAGP N RGD:5509061 20171026 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0030250 frontonasal prominence hypoplasia IAGP N RGD:5509061 20171026 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0030266 small vomer bone IAGP N RGD:5509061 20171026 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0030299 lower jaw to upper jaw transformation IAGP N RGD:5509061 20171102 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0030321 abnormal tegmen tympani morphology IAGP N RGD:5509061 20171109 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0030323 short styloid process IAGP N RGD:5509061 20171109 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0030383 small presphenoid bone IAGP N RGD:5509061 20171207 MGI PMID:12434331 10476 Dlx5 distal-less homeobox 5 gene MP:0030422 abnormal outer ear cartilage morphology IAGP N RGD:5509061 20171214 MGI PMID:10433912 10476 Dlx5 distal-less homeobox 5 gene MP:0030870 abnormal superior horn of thyroid cartilage morphology IAGP N RGD:5509061 20181101 MGI PMID:10433909 10476 Dlx5 distal-less homeobox 5 gene MP:0030870 abnormal superior horn of thyroid cartilage morphology IAGP N RGD:5509061 20181101 MGI PMID:10433912 10479 Dmd dystrophin, muscular dystrophy gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10559919 10479 Dmd dystrophin, muscular dystrophy gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22076929 10479 Dmd dystrophin, muscular dystrophy gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20668298 10479 Dmd dystrophin, muscular dystrophy gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19451692 10479 Dmd dystrophin, muscular dystrophy gene MP:0000274 enlarged heart IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23831727 10479 Dmd dystrophin, muscular dystrophy gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20180215 MGI PMID:19535499 10479 Dmd dystrophin, muscular dystrophy gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19451692 10479 Dmd dystrophin, muscular dystrophy gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:9626497 10479 Dmd dystrophin, muscular dystrophy gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:17668421 10479 Dmd dystrophin, muscular dystrophy gene MP:0000730 increased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:17961534 10479 Dmd dystrophin, muscular dystrophy gene MP:0000730 increased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:20705734 10479 Dmd dystrophin, muscular dystrophy gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:20705734 10479 Dmd dystrophin, muscular dystrophy gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20180215 MGI PMID:19535499 10479 Dmd dystrophin, muscular dystrophy gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:10792059 10479 Dmd dystrophin, muscular dystrophy gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:20668298 10479 Dmd dystrophin, muscular dystrophy gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0000747 muscle weakness IAGP N RGD:5509061 20151008 MGI PMID:20304955 10479 Dmd dystrophin, muscular dystrophy gene MP:0000747 muscle weakness IAGP N RGD:5509061 20200402 MGI PMID:31028078 10479 Dmd dystrophin, muscular dystrophy gene MP:0000747 muscle weakness IAGP N RGD:5509061 20200723 MGI PMID:30854433 10479 Dmd dystrophin, muscular dystrophy gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:22076929 10479 Dmd dystrophin, muscular dystrophy gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:22279050 10479 Dmd dystrophin, muscular dystrophy gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:9299538 10479 Dmd dystrophin, muscular dystrophy gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20170525 MGI PMID:26365037 10479 Dmd dystrophin, muscular dystrophy gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:9284044 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:10559919 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:12917328 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:20371627 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:20668298 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:22734004 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:9681470 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20160714 MGI PMID:26966179 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20170525 MGI PMID:26365037 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20170706 MGI PMID:25530839 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20180712 MGI PMID:29187645 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20200402 MGI PMID:31028078 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20200723 MGI PMID:30854433 10479 Dmd dystrophin, muscular dystrophy gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20210311 MGI PMID:28505980 10479 Dmd dystrophin, muscular dystrophy gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10204788 10479 Dmd dystrophin, muscular dystrophy gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12917328 10479 Dmd dystrophin, muscular dystrophy gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:18385524 10479 Dmd dystrophin, muscular dystrophy gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:3239377 10479 Dmd dystrophin, muscular dystrophy gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:22076929 10479 Dmd dystrophin, muscular dystrophy gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:10719885 10479 Dmd dystrophin, muscular dystrophy gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:1686056 10479 Dmd dystrophin, muscular dystrophy gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20705734 10479 Dmd dystrophin, muscular dystrophy gene MP:0001260 increased body weight IAGP N RGD:5509061 20170525 MGI PMID:26365037 10479 Dmd dystrophin, muscular dystrophy gene MP:0001260 increased body weight IAGP N RGD:5509061 20200402 MGI PMID:31028078 10479 Dmd dystrophin, muscular dystrophy gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20371627 10479 Dmd dystrophin, muscular dystrophy gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21893021 10479 Dmd dystrophin, muscular dystrophy gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22279050 10479 Dmd dystrophin, muscular dystrophy gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151008 MGI PMID:20304955 10479 Dmd dystrophin, muscular dystrophy gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0001264 increased body size IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10792059 10479 Dmd dystrophin, muscular dystrophy gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20371627 10479 Dmd dystrophin, muscular dystrophy gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22076929 10479 Dmd dystrophin, muscular dystrophy gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0001265 decreased body size IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10792059 10479 Dmd dystrophin, muscular dystrophy gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22076929 10479 Dmd dystrophin, muscular dystrophy gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16540561 10479 Dmd dystrophin, muscular dystrophy gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20668298 10479 Dmd dystrophin, muscular dystrophy gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21893021 10479 Dmd dystrophin, muscular dystrophy gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20668298 10479 Dmd dystrophin, muscular dystrophy gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21893021 10479 Dmd dystrophin, muscular dystrophy gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22076929 10479 Dmd dystrophin, muscular dystrophy gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:21893021 10479 Dmd dystrophin, muscular dystrophy gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:16540561 10479 Dmd dystrophin, muscular dystrophy gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:18385524 10479 Dmd dystrophin, muscular dystrophy gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:20705734 10479 Dmd dystrophin, muscular dystrophy gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10559919 10479 Dmd dystrophin, muscular dystrophy gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0001853 heart inflammation IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:24200690 10479 Dmd dystrophin, muscular dystrophy gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:17668421 10479 Dmd dystrophin, muscular dystrophy gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:8099842 10479 Dmd dystrophin, muscular dystrophy gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15694376 10479 Dmd dystrophin, muscular dystrophy gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8099842 10479 Dmd dystrophin, muscular dystrophy gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10559919 10479 Dmd dystrophin, muscular dystrophy gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10792059 10479 Dmd dystrophin, muscular dystrophy gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20668298 10479 Dmd dystrophin, muscular dystrophy gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23831727 10479 Dmd dystrophin, muscular dystrophy gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9874799 10479 Dmd dystrophin, muscular dystrophy gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:12917328 10479 Dmd dystrophin, muscular dystrophy gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19401296 10479 Dmd dystrophin, muscular dystrophy gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19451692 10479 Dmd dystrophin, muscular dystrophy gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:2144875 10479 Dmd dystrophin, muscular dystrophy gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:8433102 10479 Dmd dystrophin, muscular dystrophy gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:9626497 10479 Dmd dystrophin, muscular dystrophy gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15694130 10479 Dmd dystrophin, muscular dystrophy gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19401296 10479 Dmd dystrophin, muscular dystrophy gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9626497 10479 Dmd dystrophin, muscular dystrophy gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:10559919 10479 Dmd dystrophin, muscular dystrophy gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:9626497 10479 Dmd dystrophin, muscular dystrophy gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:20705734 10479 Dmd dystrophin, muscular dystrophy gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12904583 10479 Dmd dystrophin, muscular dystrophy gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15694376 10479 Dmd dystrophin, muscular dystrophy gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:15694130 10479 Dmd dystrophin, muscular dystrophy gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:1635838 10479 Dmd dystrophin, muscular dystrophy gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:1865908 10479 Dmd dystrophin, muscular dystrophy gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:22076929 10479 Dmd dystrophin, muscular dystrophy gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:9284044 10479 Dmd dystrophin, muscular dystrophy gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:9299538 10479 Dmd dystrophin, muscular dystrophy gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:1865908 10479 Dmd dystrophin, muscular dystrophy gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20180215 MGI PMID:19535499 10479 Dmd dystrophin, muscular dystrophy gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 10479 Dmd dystrophin, muscular dystrophy gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:23831727 10479 Dmd dystrophin, muscular dystrophy gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:23831727 10479 Dmd dystrophin, muscular dystrophy gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:9874799 10479 Dmd dystrophin, muscular dystrophy gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:9874799 10479 Dmd dystrophin, muscular dystrophy gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17668421 10479 Dmd dystrophin, muscular dystrophy gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21893021 10479 Dmd dystrophin, muscular dystrophy gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0002899 fatigue IAGP N RGD:5509061 20141003 MGI PMID:21893021 10479 Dmd dystrophin, muscular dystrophy gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20210520 MGI 10479 Dmd dystrophin, muscular dystrophy gene MP:0002952 ventricular cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:23831727 10479 Dmd dystrophin, muscular dystrophy gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20180215 MGI PMID:19535499 10479 Dmd dystrophin, muscular dystrophy gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20221215 MGI 10479 Dmd dystrophin, muscular dystrophy gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 10479 Dmd dystrophin, muscular dystrophy gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20151008 MGI PMID:20304955 10479 Dmd dystrophin, muscular dystrophy gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12917328 10479 Dmd dystrophin, muscular dystrophy gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17961534 10479 Dmd dystrophin, muscular dystrophy gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20705734 10479 Dmd dystrophin, muscular dystrophy gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:2407807 10479 Dmd dystrophin, muscular dystrophy gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:2919177 10479 Dmd dystrophin, muscular dystrophy gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:2967442 10479 Dmd dystrophin, muscular dystrophy gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:3209690 10479 Dmd dystrophin, muscular dystrophy gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:3239377 10479 Dmd dystrophin, muscular dystrophy gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:3440862 10479 Dmd dystrophin, muscular dystrophy gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20160714 MGI PMID:26966179 10479 Dmd dystrophin, muscular dystrophy gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20180215 MGI PMID:19535499 10479 Dmd dystrophin, muscular dystrophy gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23831727 10479 Dmd dystrophin, muscular dystrophy gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:24200690 10479 Dmd dystrophin, muscular dystrophy gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:2919177 10479 Dmd dystrophin, muscular dystrophy gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9874799 10479 Dmd dystrophin, muscular dystrophy gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:2919177 10479 Dmd dystrophin, muscular dystrophy gene MP:0003199 calcified muscle IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0003199 calcified muscle IAGP N RGD:5509061 20170713 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0003358 abnormal hypaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9284044 10479 Dmd dystrophin, muscular dystrophy gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:21893021 10479 Dmd dystrophin, muscular dystrophy gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23831727 10479 Dmd dystrophin, muscular dystrophy gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:17668421 10479 Dmd dystrophin, muscular dystrophy gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210520 MGI 10479 Dmd dystrophin, muscular dystrophy gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:12917328 10479 Dmd dystrophin, muscular dystrophy gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:10559919 10479 Dmd dystrophin, muscular dystrophy gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:10792059 10479 Dmd dystrophin, muscular dystrophy gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:15694130 10479 Dmd dystrophin, muscular dystrophy gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:3239377 10479 Dmd dystrophin, muscular dystrophy gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20180712 MGI PMID:29187645 10479 Dmd dystrophin, muscular dystrophy gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:19401296 10479 Dmd dystrophin, muscular dystrophy gene MP:0003950 abnormal plasma membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11432672 10479 Dmd dystrophin, muscular dystrophy gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210520 MGI 10479 Dmd dystrophin, muscular dystrophy gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20181220 MGI PMID:28592916 10479 Dmd dystrophin, muscular dystrophy gene MP:0004036 abnormal muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:16857961 10479 Dmd dystrophin, muscular dystrophy gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20180215 MGI PMID:19535499 10479 Dmd dystrophin, muscular dystrophy gene MP:0004089 dilated sarcoplasmic reticulum IAGP N RGD:5509061 20141003 MGI PMID:3239377 10479 Dmd dystrophin, muscular dystrophy gene MP:0004089 dilated sarcoplasmic reticulum IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:22734004 10479 Dmd dystrophin, muscular dystrophy gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:24200690 10479 Dmd dystrophin, muscular dystrophy gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20200402 MGI PMID:31028078 10479 Dmd dystrophin, muscular dystrophy gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20181220 MGI PMID:28592916 10479 Dmd dystrophin, muscular dystrophy gene MP:0004142 abnormal muscle tone IAGP N RGD:5509061 20141003 MGI PMID:3209690 10479 Dmd dystrophin, muscular dystrophy gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:2250175 10479 Dmd dystrophin, muscular dystrophy gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:12917328 10479 Dmd dystrophin, muscular dystrophy gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:9284044 10479 Dmd dystrophin, muscular dystrophy gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:16857961 10479 Dmd dystrophin, muscular dystrophy gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:22076929 10479 Dmd dystrophin, muscular dystrophy gene MP:0004248 abnormal epaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9284044 10479 Dmd dystrophin, muscular dystrophy gene MP:0004262 abnormal physical strength IAGP N RGD:5509061 20141003 MGI PMID:19451692 10479 Dmd dystrophin, muscular dystrophy gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:20371627 10479 Dmd dystrophin, muscular dystrophy gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0004510 myositis IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0004510 myositis IAGP N RGD:5509061 20160929 MGI PMID:17889902 10479 Dmd dystrophin, muscular dystrophy gene MP:0004510 myositis IAGP N RGD:5509061 20170525 MGI PMID:26365037 10479 Dmd dystrophin, muscular dystrophy gene MP:0004510 myositis IAGP N RGD:5509061 20180712 MGI PMID:29187645 10479 Dmd dystrophin, muscular dystrophy gene MP:0004510 myositis IAGP N RGD:5509061 20200723 MGI PMID:30854433 10479 Dmd dystrophin, muscular dystrophy gene MP:0004510 myositis IAGP N RGD:5509061 20210311 MGI PMID:28505980 10479 Dmd dystrophin, muscular dystrophy gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:9874799 10479 Dmd dystrophin, muscular dystrophy gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:2919177 10479 Dmd dystrophin, muscular dystrophy gene MP:0004597 increased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12148865 10479 Dmd dystrophin, muscular dystrophy gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:17668421 10479 Dmd dystrophin, muscular dystrophy gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:8186696 10479 Dmd dystrophin, muscular dystrophy gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20151008 MGI PMID:20304955 10479 Dmd dystrophin, muscular dystrophy gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20151008 MGI PMID:20304955 10479 Dmd dystrophin, muscular dystrophy gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19451692 10479 Dmd dystrophin, muscular dystrophy gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19451692 10479 Dmd dystrophin, muscular dystrophy gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17668421 10479 Dmd dystrophin, muscular dystrophy gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19451692 10479 Dmd dystrophin, muscular dystrophy gene MP:0005137 increased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:8064326 10479 Dmd dystrophin, muscular dystrophy gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22810924 10479 Dmd dystrophin, muscular dystrophy gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:24200690 10479 Dmd dystrophin, muscular dystrophy gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20181220 MGI PMID:28592916 10479 Dmd dystrophin, muscular dystrophy gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9874799 10479 Dmd dystrophin, muscular dystrophy gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:10559919 10479 Dmd dystrophin, muscular dystrophy gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:24200690 10479 Dmd dystrophin, muscular dystrophy gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20210520 MGI 10479 Dmd dystrophin, muscular dystrophy gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:20668298 10479 Dmd dystrophin, muscular dystrophy gene MP:0005505 thrombocytosis IEA N RGD:5509061 20210520 MGI 10479 Dmd dystrophin, muscular dystrophy gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12040037 10479 Dmd dystrophin, muscular dystrophy gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10068512 10479 Dmd dystrophin, muscular dystrophy gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:7843915 10479 Dmd dystrophin, muscular dystrophy gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 10479 Dmd dystrophin, muscular dystrophy gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 10479 Dmd dystrophin, muscular dystrophy gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:23831727 10479 Dmd dystrophin, muscular dystrophy gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:24200690 10479 Dmd dystrophin, muscular dystrophy gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9874799 10479 Dmd dystrophin, muscular dystrophy gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18385524 10479 Dmd dystrophin, muscular dystrophy gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20705734 10479 Dmd dystrophin, muscular dystrophy gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:3440862 10479 Dmd dystrophin, muscular dystrophy gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:2967442 10479 Dmd dystrophin, muscular dystrophy gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:9288752 10479 Dmd dystrophin, muscular dystrophy gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:9874799 10479 Dmd dystrophin, muscular dystrophy gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20181220 MGI PMID:28592916 10479 Dmd dystrophin, muscular dystrophy gene MP:0006190 retina ischemia IAGP N RGD:5509061 20141003 MGI PMID:12812982 10479 Dmd dystrophin, muscular dystrophy gene MP:0008327 abnormal corticotroph morphology IAGP N RGD:5509061 20141003 MGI PMID:8064326 10479 Dmd dystrophin, muscular dystrophy gene MP:0008416 increased somatotroph cell size IAGP N RGD:5509061 20150129 MGI PMID:8064326 10479 Dmd dystrophin, muscular dystrophy gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200402 MGI PMID:31028078 10479 Dmd dystrophin, muscular dystrophy gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19451692 10479 Dmd dystrophin, muscular dystrophy gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19451692 10479 Dmd dystrophin, muscular dystrophy gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:19451692 10479 Dmd dystrophin, muscular dystrophy gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19451692 10479 Dmd dystrophin, muscular dystrophy gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19451692 10479 Dmd dystrophin, muscular dystrophy gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:19451692 10479 Dmd dystrophin, muscular dystrophy gene MP:0008837 increased transforming growth factor beta level IAGP N RGD:5509061 20141003 MGI PMID:17668421 10479 Dmd dystrophin, muscular dystrophy gene MP:0008838 decreased transforming growth factor beta level IAGP N RGD:5509061 20141003 MGI PMID:17668421 10479 Dmd dystrophin, muscular dystrophy gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:8047301 10479 Dmd dystrophin, muscular dystrophy gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20181220 MGI PMID:28592916 10479 Dmd dystrophin, muscular dystrophy gene MP:0009398 abnormal skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:20705734 10479 Dmd dystrophin, muscular dystrophy gene MP:0009398 abnormal skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:15694130 10479 Dmd dystrophin, muscular dystrophy gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:15694376 10479 Dmd dystrophin, muscular dystrophy gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:15694130 10479 Dmd dystrophin, muscular dystrophy gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:20371627 10479 Dmd dystrophin, muscular dystrophy gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:17668421 10479 Dmd dystrophin, muscular dystrophy gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:17961534 10479 Dmd dystrophin, muscular dystrophy gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:3209690 10479 Dmd dystrophin, muscular dystrophy gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:8186696 10479 Dmd dystrophin, muscular dystrophy gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:20371627 10479 Dmd dystrophin, muscular dystrophy gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20200402 MGI PMID:31028078 10479 Dmd dystrophin, muscular dystrophy gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:12917328 10479 Dmd dystrophin, muscular dystrophy gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:18385524 10479 Dmd dystrophin, muscular dystrophy gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:20705734 10479 Dmd dystrophin, muscular dystrophy gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:22076929 10479 Dmd dystrophin, muscular dystrophy gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:8099842 10479 Dmd dystrophin, muscular dystrophy gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20180712 MGI PMID:29187645 10479 Dmd dystrophin, muscular dystrophy gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20201224 MGI PMID:32483152 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:1635838 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:17668421 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:17961534 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:18385524 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:20705734 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:22734004 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:22810924 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:2967442 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:3440862 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:8186696 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:9288751 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20160714 MGI PMID:26966179 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20180215 MGI PMID:19535499 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20180712 MGI PMID:29187645 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20200402 MGI PMID:31028078 10479 Dmd dystrophin, muscular dystrophy gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20200723 MGI PMID:30854433 10479 Dmd dystrophin, muscular dystrophy gene MP:0009405 increased skeletal muscle fiber number IAGP N RGD:5509061 20151008 MGI PMID:20304955 10479 Dmd dystrophin, muscular dystrophy gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20151008 MGI PMID:20304955 10479 Dmd dystrophin, muscular dystrophy gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20181220 MGI PMID:28592916 10479 Dmd dystrophin, muscular dystrophy gene MP:0009410 abnormal skeletal muscle satellite cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22279050 10479 Dmd dystrophin, muscular dystrophy gene MP:0009410 abnormal skeletal muscle satellite cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:3239377 10479 Dmd dystrophin, muscular dystrophy gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:15694376 10479 Dmd dystrophin, muscular dystrophy gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:17668421 10479 Dmd dystrophin, muscular dystrophy gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:20371627 10479 Dmd dystrophin, muscular dystrophy gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:2919177 10479 Dmd dystrophin, muscular dystrophy gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20200402 MGI PMID:31028078 10479 Dmd dystrophin, muscular dystrophy gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20200723 MGI PMID:30854433 10479 Dmd dystrophin, muscular dystrophy gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:12917328 10479 Dmd dystrophin, muscular dystrophy gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:15694376 10479 Dmd dystrophin, muscular dystrophy gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:17961534 10479 Dmd dystrophin, muscular dystrophy gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:22076929 10479 Dmd dystrophin, muscular dystrophy gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:2967442 10479 Dmd dystrophin, muscular dystrophy gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:3239377 10479 Dmd dystrophin, muscular dystrophy gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:3440862 10479 Dmd dystrophin, muscular dystrophy gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:8186696 10479 Dmd dystrophin, muscular dystrophy gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20160714 MGI PMID:26966179 10479 Dmd dystrophin, muscular dystrophy gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20170525 MGI PMID:26365037 10479 Dmd dystrophin, muscular dystrophy gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20200402 MGI PMID:31028078 10479 Dmd dystrophin, muscular dystrophy gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:21931825 10479 Dmd dystrophin, muscular dystrophy gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0009416 cardiac muscle degeneration IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10792059 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:1635838 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17668421 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20668298 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21893021 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22076929 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22279050 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20151008 MGI PMID:20304955 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20160714 MGI PMID:26966179 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20200402 MGI PMID:31028078 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20200716 MGI PMID:26365037 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20200723 MGI PMID:30854433 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20201224 MGI PMID:32483152 10479 Dmd dystrophin, muscular dystrophy gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20210311 MGI PMID:28505980 10479 Dmd dystrophin, muscular dystrophy gene MP:0009420 skeletal muscle endomysial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22076929 10479 Dmd dystrophin, muscular dystrophy gene MP:0009420 skeletal muscle endomysial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:8186696 10479 Dmd dystrophin, muscular dystrophy gene MP:0009420 skeletal muscle endomysial fibrosis IAGP N RGD:5509061 20160929 MGI PMID:17889902 10479 Dmd dystrophin, muscular dystrophy gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:8186696 10479 Dmd dystrophin, muscular dystrophy gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20151008 MGI PMID:20304955 10479 Dmd dystrophin, muscular dystrophy gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 10479 Dmd dystrophin, muscular dystrophy gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20371627 10479 Dmd dystrophin, muscular dystrophy gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:21893021 10479 Dmd dystrophin, muscular dystrophy gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20170525 MGI PMID:26365037 10479 Dmd dystrophin, muscular dystrophy gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20180712 MGI PMID:29187645 10479 Dmd dystrophin, muscular dystrophy gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200723 MGI PMID:30854433 10479 Dmd dystrophin, muscular dystrophy gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210826 MGI 10479 Dmd dystrophin, muscular dystrophy gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:22810924 10479 Dmd dystrophin, muscular dystrophy gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:2967442 10479 Dmd dystrophin, muscular dystrophy gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:8064326 10479 Dmd dystrophin, muscular dystrophy gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20160714 MGI PMID:26966179 10479 Dmd dystrophin, muscular dystrophy gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20170525 MGI PMID:26365037 10479 Dmd dystrophin, muscular dystrophy gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20200402 MGI PMID:31028078 10479 Dmd dystrophin, muscular dystrophy gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20200723 MGI PMID:30854433 10479 Dmd dystrophin, muscular dystrophy gene MP:0010106 abnormal circulating pyruvate kinase level IAGP N RGD:5509061 20141003 MGI PMID:6583703 10479 Dmd dystrophin, muscular dystrophy gene MP:0010106 abnormal circulating pyruvate kinase level IAGP N RGD:5509061 20141003 MGI PMID:9681470 10479 Dmd dystrophin, muscular dystrophy gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 10479 Dmd dystrophin, muscular dystrophy gene MP:0010226 increased quadriceps weight IAGP N RGD:5509061 20151008 MGI PMID:20304955 10479 Dmd dystrophin, muscular dystrophy gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20151008 MGI PMID:20304955 10479 Dmd dystrophin, muscular dystrophy gene MP:0010238 increased skeletal muscle weight IAGP N RGD:5509061 20151008 MGI PMID:20304955 10479 Dmd dystrophin, muscular dystrophy gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:20371627 10479 Dmd dystrophin, muscular dystrophy gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:22279050 10479 Dmd dystrophin, muscular dystrophy gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20151008 MGI PMID:20304955 10479 Dmd dystrophin, muscular dystrophy gene MP:0010252 anterior subcapsular cataract IAGP N RGD:5509061 20141003 MGI PMID:2250175 10479 Dmd dystrophin, muscular dystrophy gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:2250175 10479 Dmd dystrophin, muscular dystrophy gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:16857961 10479 Dmd dystrophin, muscular dystrophy gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:23831727 10479 Dmd dystrophin, muscular dystrophy gene MP:0010509 decreased P wave amplitude IAGP N RGD:5509061 20141003 MGI PMID:16857961 10479 Dmd dystrophin, muscular dystrophy gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:23831727 10479 Dmd dystrophin, muscular dystrophy gene MP:0010581 abnormal atrium myocardial trabeculae morphology IAGP N RGD:5509061 20180215 MGI PMID:19535499 10479 Dmd dystrophin, muscular dystrophy gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:20668298 10479 Dmd dystrophin, muscular dystrophy gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10559919 10479 Dmd dystrophin, muscular dystrophy gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10792059 10479 Dmd dystrophin, muscular dystrophy gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22076929 10479 Dmd dystrophin, muscular dystrophy gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8099842 10479 Dmd dystrophin, muscular dystrophy gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:23831727 10479 Dmd dystrophin, muscular dystrophy gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:23831727 10479 Dmd dystrophin, muscular dystrophy gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20141003 MGI PMID:23831727 10479 Dmd dystrophin, muscular dystrophy gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20141003 MGI PMID:23831727 10479 Dmd dystrophin, muscular dystrophy gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20141003 MGI PMID:24200690 10479 Dmd dystrophin, muscular dystrophy gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:12148865 10479 Dmd dystrophin, muscular dystrophy gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12148865 10479 Dmd dystrophin, muscular dystrophy gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:17668421 10479 Dmd dystrophin, muscular dystrophy gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20160714 MGI PMID:26966179 10479 Dmd dystrophin, muscular dystrophy gene MP:0013237 abnormal skeletal muscle regeneration IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211104 MGI PMID:32483152 10479 Dmd dystrophin, muscular dystrophy gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:22076929 10479 Dmd dystrophin, muscular dystrophy gene MP:0013467 diaphragmitis IAGP N RGD:5509061 20160929 MGI PMID:17889902 10479 Dmd dystrophin, muscular dystrophy gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20160407 MGI PMID:21893021 10479 Dmd dystrophin, muscular dystrophy gene MP:0020280 increased creatine kinase level IAGP N RGD:5509061 20180712 MGI PMID:29187645 10479 Dmd dystrophin, muscular dystrophy gene MP:0020309 increased creatine kinase activity IAGP N RGD:5509061 20151217 MGI PMID:26566673 10479 Dmd dystrophin, muscular dystrophy gene MP:0020309 increased creatine kinase activity IAGP N RGD:5509061 20170706 MGI PMID:25530839 10479 Dmd dystrophin, muscular dystrophy gene MP:0020330 increased capillary density IAGP N RGD:5509061 20160714 MGI PMID:20705734 10479 Dmd dystrophin, muscular dystrophy gene MP:0020879 abnormal calcium level IAGP N RGD:5509061 20210311 MGI PMID:28505980 10479 Dmd dystrophin, muscular dystrophy gene MP:0020938 decreased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:24200690 10479 Dmd dystrophin, muscular dystrophy gene MP:0030428 abnormal scalene muscle morphology IAGP N RGD:5509061 20171214 MGI PMID:1865908 10479 Dmd dystrophin, muscular dystrophy gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:21145579 10479 Dmd dystrophin, muscular dystrophy gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:23831727 10479 Dmd dystrophin, muscular dystrophy gene MP:0030957 abnormal myotube morphology IAGP N RGD:5509061 20190725 MGI PMID:19535499 10479 Dmd dystrophin, muscular dystrophy gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:19535499 10479 Dmd dystrophin, muscular dystrophy gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:19401296 10479 Dmd dystrophin, muscular dystrophy gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:21931825 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200625 MGI PMID:31339932 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200702 MGI PMID:27795435 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20200625 MGI PMID:31339932 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20200709 MGI PMID:26124093 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20200402 MGI PMID:27892925 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10823914 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200402 MGI PMID:26124093 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200402 MGI PMID:27892925 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200402 MGI PMID:28348219 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200702 MGI PMID:27795435 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20200402 MGI PMID:26124093 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200402 MGI PMID:27892925 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10823914 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:10823914 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:10823914 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20200402 MGI PMID:28348219 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20200402 MGI PMID:28348219 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20200702 MGI PMID:27795435 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200625 MGI PMID:31339932 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:10823914 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23149623 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20200702 MGI PMID:27795435 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200702 MGI PMID:27795435 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200702 MGI PMID:27795435 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20200402 MGI PMID:27892925 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0010858 pulmonary epithelial necrosis IAGP N RGD:5509061 20200702 MGI PMID:27795435 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0010894 pulmonary alveolar edema IAGP N RGD:5509061 20200402 MGI PMID:27892925 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0011018 pulmonary hyaline membrane formation IAGP N RGD:5509061 20200402 MGI PMID:28348219 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0012041 increased susceptibility to pulmonary hyaline membrane formation IAGP N RGD:5509061 20200402 MGI PMID:27892925 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:26124093 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:27892925 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:28348219 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200625 MGI PMID:31339932 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200702 MGI PMID:27795435 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0031047 decreased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:27892925 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:27892925 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:28348219 10481 Dpp4 dipeptidylpeptidase 4 gene MP:0031053 pleuritis IAGP N RGD:5509061 20200702 MGI PMID:27795435 10482 Prl8a2 prolactin family 8, subfamily a, member 2 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:17166917 10482 Prl8a2 prolactin family 8, subfamily a, member 2 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:17166917 10482 Prl8a2 prolactin family 8, subfamily a, member 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17166917 10482 Prl8a2 prolactin family 8, subfamily a, member 2 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:17166917 10482 Prl8a2 prolactin family 8, subfamily a, member 2 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17166917 10482 Prl8a2 prolactin family 8, subfamily a, member 2 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17166917 10482 Prl8a2 prolactin family 8, subfamily a, member 2 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:17166917 10485 Drd1 dopamine receptor D1 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:7954836 10485 Drd1 dopamine receptor D1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7809078 10485 Drd1 dopamine receptor D1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7954836 10485 Drd1 dopamine receptor D1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10585522 10485 Drd1 dopamine receptor D1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10884517 10485 Drd1 dopamine receptor D1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11172752 10485 Drd1 dopamine receptor D1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18615733 10485 Drd1 dopamine receptor D1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7954836 10485 Drd1 dopamine receptor D1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23569242 10485 Drd1 dopamine receptor D1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:7954836 10485 Drd1 dopamine receptor D1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:8001143 10485 Drd1 dopamine receptor D1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10884517 10485 Drd1 dopamine receptor D1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10884517 10485 Drd1 dopamine receptor D1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20220421 MGI PMID:8001143 10485 Drd1 dopamine receptor D1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10585522 10485 Drd1 dopamine receptor D1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10884517 10485 Drd1 dopamine receptor D1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11172752 10485 Drd1 dopamine receptor D1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18644244 10485 Drd1 dopamine receptor D1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:7809078 10485 Drd1 dopamine receptor D1 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:7809078 10485 Drd1 dopamine receptor D1 gene MP:0001512 trunk curl IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:18615733 10485 Drd1 dopamine receptor D1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:18615733 10485 Drd1 dopamine receptor D1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:10884517 10485 Drd1 dopamine receptor D1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7809078 10485 Drd1 dopamine receptor D1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7809078 10485 Drd1 dopamine receptor D1 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:22764243 10485 Drd1 dopamine receptor D1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141120 MGI PMID:24843151 10485 Drd1 dopamine receptor D1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141120 MGI PMID:24843151 10485 Drd1 dopamine receptor D1 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:10884517 10485 Drd1 dopamine receptor D1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:10884517 10485 Drd1 dopamine receptor D1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:7809078 10485 Drd1 dopamine receptor D1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:10884517 10485 Drd1 dopamine receptor D1 gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:11172752 10485 Drd1 dopamine receptor D1 gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22356538 10485 Drd1 dopamine receptor D1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22356538 10485 Drd1 dopamine receptor D1 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20141003 MGI PMID:17409246 10485 Drd1 dopamine receptor D1 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20141120 MGI PMID:24843151 10485 Drd1 dopamine receptor D1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:8001143 10485 Drd1 dopamine receptor D1 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:19074012 10485 Drd1 dopamine receptor D1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:18615733 10485 Drd1 dopamine receptor D1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22764243 10485 Drd1 dopamine receptor D1 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17409246 10485 Drd1 dopamine receptor D1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0008802 abnormal intestinal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18486343 10485 Drd1 dopamine receptor D1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:8001143 10485 Drd1 dopamine receptor D1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141120 MGI PMID:24843151 10485 Drd1 dopamine receptor D1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20151217 MGI PMID:24496082 10485 Drd1 dopamine receptor D1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:16014726 10485 Drd1 dopamine receptor D1 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18045908 10485 Drd1 dopamine receptor D1 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:7954836 10485 Drd1 dopamine receptor D1 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:16014726 10485 Drd1 dopamine receptor D1 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:18045908 10485 Drd1 dopamine receptor D1 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:8001143 10485 Drd1 dopamine receptor D1 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18486343 10485 Drd1 dopamine receptor D1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:18615733 10485 Drd1 dopamine receptor D1 gene MP:0010167 decreased response to stress-induced hyperthermia IAGP N RGD:5509061 20141003 MGI PMID:18486343 10485 Drd1 dopamine receptor D1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15272078 10485 Drd1 dopamine receptor D1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7954836 10485 Drd1 dopamine receptor D1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141120 MGI PMID:24843151 10485 Drd1 dopamine receptor D1 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:7954836 10485 Drd1 dopamine receptor D1 gene MP:0012559 decreased forebrain volume IAGP N RGD:5509061 20141003 MGI PMID:9822743 10485 Drd1 dopamine receptor D1 gene MP:0020083 decreased hippocampus volume IAGP N RGD:5509061 20170706 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0020340 abnormal inhibitory learning IAGP N RGD:5509061 20160915 MGI PMID:10585522 10485 Drd1 dopamine receptor D1 gene MP:0030986 striatum atrophy IAGP N RGD:5509061 20191128 MGI PMID:17360497 10485 Drd1 dopamine receptor D1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:17360497 10486 Drd2 dopamine receptor D2 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11566895 10486 Drd2 dopamine receptor D2 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9247267 10486 Drd2 dopamine receptor D2 gene MP:0000635 pituitary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0000636 enlarged pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0000636 enlarged pituitary gland IAGP N RGD:5509061 20150129 MGI PMID:9247267 10486 Drd2 dopamine receptor D2 gene MP:0000646 enlarged adrenocortical cells IAGP N RGD:5509061 20141003 MGI PMID:9717839 10486 Drd2 dopamine receptor D2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:11158626 10486 Drd2 dopamine receptor D2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:7566118 10486 Drd2 dopamine receptor D2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:7566118 10486 Drd2 dopamine receptor D2 gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:9717839 10486 Drd2 dopamine receptor D2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11897683 10486 Drd2 dopamine receptor D2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11566895 10486 Drd2 dopamine receptor D2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10391470 10486 Drd2 dopamine receptor D2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10956362 10486 Drd2 dopamine receptor D2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11897683 10486 Drd2 dopamine receptor D2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16525059 10486 Drd2 dopamine receptor D2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7566118 10486 Drd2 dopamine receptor D2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10391470 10486 Drd2 dopamine receptor D2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:11069937 10486 Drd2 dopamine receptor D2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:10196569 10486 Drd2 dopamine receptor D2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:10391470 10486 Drd2 dopamine receptor D2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:9547254 10486 Drd2 dopamine receptor D2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10196569 10486 Drd2 dopamine receptor D2 gene MP:0001396 unidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:14534241 10486 Drd2 dopamine receptor D2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21743470 10486 Drd2 dopamine receptor D2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22745501 10486 Drd2 dopamine receptor D2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10196569 10486 Drd2 dopamine receptor D2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11069937 10486 Drd2 dopamine receptor D2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11864730 10486 Drd2 dopamine receptor D2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19840852 10486 Drd2 dopamine receptor D2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22745501 10486 Drd2 dopamine receptor D2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:7566118 10486 Drd2 dopamine receptor D2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22745501 10486 Drd2 dopamine receptor D2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:7566118 10486 Drd2 dopamine receptor D2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9547254 10486 Drd2 dopamine receptor D2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:7566118 10486 Drd2 dopamine receptor D2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18644244 10486 Drd2 dopamine receptor D2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:10391470 10486 Drd2 dopamine receptor D2 gene MP:0001506 limp posture IAGP N RGD:5509061 20141003 MGI PMID:7566118 10486 Drd2 dopamine receptor D2 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:18382674 10486 Drd2 dopamine receptor D2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:16525059 10486 Drd2 dopamine receptor D2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11897683 10486 Drd2 dopamine receptor D2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23536095 10486 Drd2 dopamine receptor D2 gene MP:0001744 hypersecretion of corticosterone IAGP N RGD:5509061 20141003 MGI PMID:9717839 10486 Drd2 dopamine receptor D2 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:9717839 10486 Drd2 dopamine receptor D2 gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:9717839 10486 Drd2 dopamine receptor D2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:11566895 10486 Drd2 dopamine receptor D2 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:11158626 10486 Drd2 dopamine receptor D2 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:10391470 10486 Drd2 dopamine receptor D2 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22745501 10486 Drd2 dopamine receptor D2 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22745501 10486 Drd2 dopamine receptor D2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:7566118 10486 Drd2 dopamine receptor D2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10391470 10486 Drd2 dopamine receptor D2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 10486 Drd2 dopamine receptor D2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11158626 10486 Drd2 dopamine receptor D2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22745501 10486 Drd2 dopamine receptor D2 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:23536095 10486 Drd2 dopamine receptor D2 gene MP:0002570 alcohol aversion IAGP N RGD:5509061 20141003 MGI PMID:10196569 10486 Drd2 dopamine receptor D2 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:11864730 10486 Drd2 dopamine receptor D2 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:22745501 10486 Drd2 dopamine receptor D2 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11566895 10486 Drd2 dopamine receptor D2 gene MP:0002676 uterus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9247267 10486 Drd2 dopamine receptor D2 gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:7566118 10486 Drd2 dopamine receptor D2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:11069937 10486 Drd2 dopamine receptor D2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:11864730 10486 Drd2 dopamine receptor D2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:7566118 10486 Drd2 dopamine receptor D2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:9547254 10486 Drd2 dopamine receptor D2 gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15061865 10486 Drd2 dopamine receptor D2 gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21743470 10486 Drd2 dopamine receptor D2 gene MP:0002822 catalepsy IAGP N RGD:5509061 20141003 MGI PMID:7566118 10486 Drd2 dopamine receptor D2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:11069974 10486 Drd2 dopamine receptor D2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:11158626 10486 Drd2 dopamine receptor D2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21743470 10486 Drd2 dopamine receptor D2 gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:10341260 10486 Drd2 dopamine receptor D2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:11897683 10486 Drd2 dopamine receptor D2 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17409246 10486 Drd2 dopamine receptor D2 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:11566895 10486 Drd2 dopamine receptor D2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:14534241 10486 Drd2 dopamine receptor D2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16280580 10486 Drd2 dopamine receptor D2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:9547254 10486 Drd2 dopamine receptor D2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23242137 10486 Drd2 dopamine receptor D2 gene MP:0003371 decreased circulating estrogen level IAGP N RGD:5509061 20141003 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:11897683 10486 Drd2 dopamine receptor D2 gene MP:0003462 abnormal response to novel odor IAGP N RGD:5509061 20141003 MGI PMID:16765459 10486 Drd2 dopamine receptor D2 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:14684868 10486 Drd2 dopamine receptor D2 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:21743470 10486 Drd2 dopamine receptor D2 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:9140068 10486 Drd2 dopamine receptor D2 gene MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:10196569 10486 Drd2 dopamine receptor D2 gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:11303741 10486 Drd2 dopamine receptor D2 gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:11864730 10486 Drd2 dopamine receptor D2 gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20141003 MGI PMID:16525059 10486 Drd2 dopamine receptor D2 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:23536095 10486 Drd2 dopamine receptor D2 gene MP:0003973 increased pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:9140068 10486 Drd2 dopamine receptor D2 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9247267 10486 Drd2 dopamine receptor D2 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:11897683 10486 Drd2 dopamine receptor D2 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:23536095 10486 Drd2 dopamine receptor D2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:11069974 10486 Drd2 dopamine receptor D2 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11566895 10486 Drd2 dopamine receptor D2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:11864730 10486 Drd2 dopamine receptor D2 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11897683 10486 Drd2 dopamine receptor D2 gene MP:0005117 increased circulating pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:9717839 10486 Drd2 dopamine receptor D2 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:11897683 10486 Drd2 dopamine receptor D2 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0005124 increased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:11897683 10486 Drd2 dopamine receptor D2 gene MP:0005124 increased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:23536095 10486 Drd2 dopamine receptor D2 gene MP:0005124 increased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:9247267 10486 Drd2 dopamine receptor D2 gene MP:0005124 increased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:23536095 10486 Drd2 dopamine receptor D2 gene MP:0005137 increased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:11897683 10486 Drd2 dopamine receptor D2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:10391470 10486 Drd2 dopamine receptor D2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:11069937 10486 Drd2 dopamine receptor D2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:7566118 10486 Drd2 dopamine receptor D2 gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:9140068 10486 Drd2 dopamine receptor D2 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:9140068 10486 Drd2 dopamine receptor D2 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:7566118 10486 Drd2 dopamine receptor D2 gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:10956362 10486 Drd2 dopamine receptor D2 gene MP:0005575 increased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:10956362 10486 Drd2 dopamine receptor D2 gene MP:0005576 decreased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:10956362 10486 Drd2 dopamine receptor D2 gene MP:0005585 increased tidal volume IAGP N RGD:5509061 20141003 MGI PMID:10956362 10486 Drd2 dopamine receptor D2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:19840852 10486 Drd2 dopamine receptor D2 gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:9717839 10486 Drd2 dopamine receptor D2 gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:16525059 10486 Drd2 dopamine receptor D2 gene MP:0006003 abnormal large intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:16525059 10486 Drd2 dopamine receptor D2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17409246 10486 Drd2 dopamine receptor D2 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11566895 10486 Drd2 dopamine receptor D2 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11566895 10486 Drd2 dopamine receptor D2 gene MP:0006299 abnormal latent inhibition of conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15061865 10486 Drd2 dopamine receptor D2 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:11566895 10486 Drd2 dopamine receptor D2 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11069974 10486 Drd2 dopamine receptor D2 gene MP:0008294 abnormal adrenal gland zona fasciculata morphology IAGP N RGD:5509061 20141003 MGI PMID:9717839 10486 Drd2 dopamine receptor D2 gene MP:0008295 abnormal adrenal gland zona reticularis morphology IAGP N RGD:5509061 20141003 MGI PMID:9717839 10486 Drd2 dopamine receptor D2 gene MP:0008299 adrenal cortical hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9717839 10486 Drd2 dopamine receptor D2 gene MP:0008324 abnormal melanotroph morphology IAGP N RGD:5509061 20141003 MGI PMID:9717839 10486 Drd2 dopamine receptor D2 gene MP:0008329 decreased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:23536095 10486 Drd2 dopamine receptor D2 gene MP:0008329 decreased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0008331 increased lactotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9247267 10486 Drd2 dopamine receptor D2 gene MP:0008331 increased lactotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0008335 decreased gonadotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9247267 10486 Drd2 dopamine receptor D2 gene MP:0008337 increased thyrotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0008370 enlarged pituitary intermediate lobe IAGP N RGD:5509061 20141003 MGI PMID:9140068 10486 Drd2 dopamine receptor D2 gene MP:0008371 pituitary intermediate lobe hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0008371 pituitary intermediate lobe hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9717839 10486 Drd2 dopamine receptor D2 gene MP:0008423 decreased lactotroph cell size IAGP N RGD:5509061 20141003 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:23536095 10486 Drd2 dopamine receptor D2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:23242137 10486 Drd2 dopamine receptor D2 gene MP:0008802 abnormal intestinal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11566895 10486 Drd2 dopamine receptor D2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21743470 10486 Drd2 dopamine receptor D2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9547254 10486 Drd2 dopamine receptor D2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18486343 10486 Drd2 dopamine receptor D2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21743470 10486 Drd2 dopamine receptor D2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22745501 10486 Drd2 dopamine receptor D2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23536095 10486 Drd2 dopamine receptor D2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9247267 10486 Drd2 dopamine receptor D2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9547254 10486 Drd2 dopamine receptor D2 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21743470 10486 Drd2 dopamine receptor D2 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22745501 10486 Drd2 dopamine receptor D2 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23242137 10486 Drd2 dopamine receptor D2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23242137 10486 Drd2 dopamine receptor D2 gene MP:0008939 increased pituitary gland weight IAGP N RGD:5509061 20141003 MGI PMID:9247267 10486 Drd2 dopamine receptor D2 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0009016 abnormal estrus IAGP N RGD:5509061 20141003 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0009082 uterus cyst IAGP N RGD:5509061 20141003 MGI PMID:9247267 10486 Drd2 dopamine receptor D2 gene MP:0009089 short uterine horn IAGP N RGD:5509061 20141003 MGI PMID:9247267 10486 Drd2 dopamine receptor D2 gene MP:0009221 uterus adenomyosis IAGP N RGD:5509061 20141003 MGI PMID:9247267 10486 Drd2 dopamine receptor D2 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11897683 10486 Drd2 dopamine receptor D2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:9252189 10486 Drd2 dopamine receptor D2 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11069937 10486 Drd2 dopamine receptor D2 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12650980 10486 Drd2 dopamine receptor D2 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11089973 10486 Drd2 dopamine receptor D2 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22745501 10486 Drd2 dopamine receptor D2 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11069937 10486 Drd2 dopamine receptor D2 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11089973 10486 Drd2 dopamine receptor D2 gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:10341260 10486 Drd2 dopamine receptor D2 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:21743470 10486 Drd2 dopamine receptor D2 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:22745501 10486 Drd2 dopamine receptor D2 gene MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:10196569 10486 Drd2 dopamine receptor D2 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:22745501 10486 Drd2 dopamine receptor D2 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18486343 10486 Drd2 dopamine receptor D2 gene MP:0009778 impaired behavioral response to anesthetic IAGP N RGD:5509061 20141003 MGI PMID:22745501 10486 Drd2 dopamine receptor D2 gene MP:0009779 enhanced behavioral response to anesthetic IAGP N RGD:5509061 20141003 MGI PMID:22745501 10486 Drd2 dopamine receptor D2 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20141003 MGI PMID:21743470 10486 Drd2 dopamine receptor D2 gene MP:0010167 decreased response to stress-induced hyperthermia IAGP N RGD:5509061 20141003 MGI PMID:18486343 10486 Drd2 dopamine receptor D2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15272078 10486 Drd2 dopamine receptor D2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10391470 10486 Drd2 dopamine receptor D2 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:14534241 10486 Drd2 dopamine receptor D2 gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:23242137 10486 Drd2 dopamine receptor D2 gene MP:0011532 decreased urine major urinary protein level IAGP N RGD:5509061 20141003 MGI PMID:23536095 10486 Drd2 dopamine receptor D2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:11897683 10486 Drd2 dopamine receptor D2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:16525059 10486 Drd2 dopamine receptor D2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:7566118 10486 Drd2 dopamine receptor D2 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:16525059 10486 Drd2 dopamine receptor D2 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:7566118 10486 Drd2 dopamine receptor D2 gene MP:0013334 adenohypophysis peliosis IAGP N RGD:5509061 20141204 MGI PMID:9247267 10486 Drd2 dopamine receptor D2 gene MP:0013348 adenohypophysis hyperplasia IAGP N RGD:5509061 20150129 MGI PMID:9247267 10486 Drd2 dopamine receptor D2 gene MP:0013348 adenohypophysis hyperplasia IAGP N RGD:5509061 20150129 MGI PMID:9247268 10486 Drd2 dopamine receptor D2 gene MP:0013355 adenohypophysis hypertrophy IAGP N RGD:5509061 20150129 MGI PMID:9247267 10487 Drd4 dopamine receptor D4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9323127 10487 Drd4 dopamine receptor D4 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:10531457 10487 Drd4 dopamine receptor D4 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:9323127 10487 Drd4 dopamine receptor D4 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:22764243 10487 Drd4 dopamine receptor D4 gene MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20141003 MGI PMID:9323127 10487 Drd4 dopamine receptor D4 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:9323127 10487 Drd4 dopamine receptor D4 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:14684868 10487 Drd4 dopamine receptor D4 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:9323127 10487 Drd4 dopamine receptor D4 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22764243 10487 Drd4 dopamine receptor D4 gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:9323127 10487 Drd4 dopamine receptor D4 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:9323127 10489 Drd5 dopamine receptor D5 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:12486173 10489 Drd5 dopamine receptor D5 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:15598876 10489 Drd5 dopamine receptor D5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141120 MGI PMID:24843151 10489 Drd5 dopamine receptor D5 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141120 MGI PMID:24843151 10489 Drd5 dopamine receptor D5 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12486173 10489 Drd5 dopamine receptor D5 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12486173 10489 Drd5 dopamine receptor D5 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15598876 10489 Drd5 dopamine receptor D5 gene MP:0002909 abnormal adrenal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:12486173 10489 Drd5 dopamine receptor D5 gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20141120 MGI PMID:24843151 10489 Drd5 dopamine receptor D5 gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12486173 10489 Drd5 dopamine receptor D5 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12486173 10489 Drd5 dopamine receptor D5 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15598876 10489 Drd5 dopamine receptor D5 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12486173 10489 Drd5 dopamine receptor D5 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15598876 10489 Drd5 dopamine receptor D5 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141120 MGI PMID:24843151 10489 Drd5 dopamine receptor D5 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141120 MGI PMID:24843151 10489 Drd5 dopamine receptor D5 gene MP:0031303 enhanced behavioral response to methamphetamine IAGP N RGD:5509061 20211028 MGI PMID:24155877 10493 Dspp dentin sialophosphoprotein gene MP:0000126 brittle teeth IAGP N RGD:5509061 20141003 MGI PMID:12721295 10493 Dspp dentin sialophosphoprotein gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20190207 MGI PMID:16937369 10493 Dspp dentin sialophosphoprotein gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20190207 MGI PMID:16937369 10493 Dspp dentin sialophosphoprotein gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:12721295 10493 Dspp dentin sialophosphoprotein gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170105 MGI 10493 Dspp dentin sialophosphoprotein gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20141003 MGI PMID:12721295 10493 Dspp dentin sialophosphoprotein gene MP:0002819 abnormal dental pulp cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:12721295 10493 Dspp dentin sialophosphoprotein gene MP:0003668 abnormal periodontal ligament morphology IAGP N RGD:5509061 20171026 MGI PMID:22934831 10493 Dspp dentin sialophosphoprotein gene MP:0003933 abnormal cementum morphology IAGP N RGD:5509061 20171026 MGI PMID:22934831 10493 Dspp dentin sialophosphoprotein gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20171026 MGI PMID:22934831 10493 Dspp dentin sialophosphoprotein gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 10493 Dspp dentin sialophosphoprotein gene MP:0008528 polycystic kidney IEA N RGD:5509061 20170105 MGI 10493 Dspp dentin sialophosphoprotein gene MP:0011035 abnormal branching involved in alveolar duct morphogenesis IAGP N RGD:5509061 20190207 MGI PMID:16937369 10493 Dspp dentin sialophosphoprotein gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 10493 Dspp dentin sialophosphoprotein gene MP:0011365 small metanephros IAGP N RGD:5509061 20190207 MGI PMID:16937369 10493 Dspp dentin sialophosphoprotein gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20190207 MGI PMID:16937369 10493 Dspp dentin sialophosphoprotein gene MP:0011457 abnormal metanephric ureteric bud development IAGP N RGD:5509061 20190207 MGI PMID:16937369 10493 Dspp dentin sialophosphoprotein gene MP:0012024 abnormal nephron morphogenesis IAGP N RGD:5509061 20190207 MGI PMID:16937369 10493 Dspp dentin sialophosphoprotein gene MP:0012026 abnormal S-shaped body morphology IAGP N RGD:5509061 20190207 MGI PMID:16937369 10493 Dspp dentin sialophosphoprotein gene MP:0030131 abnormal periodontium morphology IAGP N RGD:5509061 20171026 MGI PMID:22934831 10493 Dspp dentin sialophosphoprotein gene MP:0030132 periodontium inflammation IAGP N RGD:5509061 20171026 MGI PMID:22934831 10493 Dspp dentin sialophosphoprotein gene MP:0030451 abnormal dentin mineralization IAGP N RGD:5509061 20171221 MGI PMID:12721295 10493 Dspp dentin sialophosphoprotein gene MP:0030466 alveolar process atrophy IAGP N RGD:5509061 20171221 MGI PMID:12721295 10493 Dspp dentin sialophosphoprotein gene MP:0030466 alveolar process atrophy IAGP N RGD:5509061 20171221 MGI PMID:22934831 10493 Dspp dentin sialophosphoprotein gene MP:0030484 abnormal osteocyte lacuna morphology IAGP N RGD:5509061 20171221 MGI PMID:22934831 10493 Dspp dentin sialophosphoprotein gene MP:0030486 abnormal osteocyte canaliculus morphology IAGP N RGD:5509061 20171221 MGI PMID:22934831 10493 Dspp dentin sialophosphoprotein gene MP:0030490 periodontal pocket IAGP N RGD:5509061 20180111 MGI PMID:22934831 10493 Dspp dentin sialophosphoprotein gene MP:0030516 abnormal junctional epithelium morphology IAGP N RGD:5509061 20180111 MGI PMID:22934831 10493 Dspp dentin sialophosphoprotein gene MP:0030517 detached junctional epithelium IAGP N RGD:5509061 20180111 MGI PMID:22934831 10493 Dspp dentin sialophosphoprotein gene MP:0030543 abnormal predentin morphology IAGP N RGD:5509061 20180215 MGI PMID:12721295 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:16137572 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20150910 MGI PMID:26008897 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0000771 abnormal brain size IAGP N RGD:5509061 20141003 MGI PMID:22293606 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:22293606 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:22293606 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22293606 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220512 MGI PMID:29223763 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20151022 MGI PMID:26374847 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20220512 MGI PMID:29223763 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20220512 MGI PMID:29223763 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20220512 MGI PMID:29223763 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0002892 decreased superior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20150910 MGI PMID:26008897 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20220512 MGI PMID:29223763 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20151022 MGI PMID:26374847 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20150910 MGI PMID:26008897 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20150910 MGI PMID:26008897 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0006105 small tectum IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20150910 MGI PMID:26008897 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20150910 MGI PMID:26008897 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20150910 MGI PMID:26008897 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20150910 MGI PMID:26008897 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20220512 MGI PMID:29223763 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20220512 MGI PMID:29223763 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20220512 MGI PMID:29223763 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20151022 MGI PMID:26374847 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16137572 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20151022 MGI PMID:26374847 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0012088 abnormal midbrain size IAGP N RGD:5509061 20220512 MGI PMID:29223763 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0012263 decreased hindbrain size IAGP N RGD:5509061 20141003 MGI PMID:12192061 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20220512 MGI PMID:29223763 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0014115 cognitive inflexibility IAGP N RGD:5509061 20220512 MGI PMID:29223763 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0020083 decreased hippocampus volume IAGP N RGD:5509061 20170706 MGI PMID:22293606 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20220512 MGI PMID:29223763 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0020568 abnormal premotor cortex morphology IAGP N RGD:5509061 20180315 MGI PMID:16137572 10495 Dyrk1a dual-specificity tyrosine phosphorylation regulated kinase 1a gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20220512 MGI PMID:29223763 10499 Edn1 endothelin 1 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:8152482 10499 Edn1 endothelin 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:8152482 10499 Edn1 endothelin 1 gene MP:0000114 cleft chin IAGP N RGD:5509061 20141003 MGI PMID:8152482 10499 Edn1 endothelin 1 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:15314687 10499 Edn1 endothelin 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:7615798 10499 Edn1 endothelin 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:7615798 10499 Edn1 endothelin 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:7615798 10499 Edn1 endothelin 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:20516397 10499 Edn1 endothelin 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8152482 10499 Edn1 endothelin 1 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:8152482 10499 Edn1 endothelin 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:7615798 10499 Edn1 endothelin 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20200227 MGI PMID:20516397 10499 Edn1 endothelin 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:15632412 10499 Edn1 endothelin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20516397 10499 Edn1 endothelin 1 gene MP:0002318 hypercapnia IAGP N RGD:5509061 20141003 MGI PMID:10626068 10499 Edn1 endothelin 1 gene MP:0002329 abnormal blood gas level IAGP N RGD:5509061 20141003 MGI PMID:10626068 10499 Edn1 endothelin 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:7615798 10499 Edn1 endothelin 1 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:7615798 10499 Edn1 endothelin 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:8152482 10499 Edn1 endothelin 1 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8152482 10499 Edn1 endothelin 1 gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:15632412 10499 Edn1 endothelin 1 gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20221103 MGI PMID:8152482 10499 Edn1 endothelin 1 gene MP:0004181 abnormal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:7615798 10499 Edn1 endothelin 1 gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:10626068 10499 Edn1 endothelin 1 gene MP:0004205 absent hyoid bone IAGP N RGD:5509061 20141003 MGI PMID:8152482 10499 Edn1 endothelin 1 gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20141003 MGI PMID:15314687 10499 Edn1 endothelin 1 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:12193100 10499 Edn1 endothelin 1 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:14764893 10499 Edn1 endothelin 1 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10626068 10499 Edn1 endothelin 1 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20516397 10499 Edn1 endothelin 1 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:10626068 10499 Edn1 endothelin 1 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:8152482 10499 Edn1 endothelin 1 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:8152482 10499 Edn1 endothelin 1 gene MP:0005611 decreased circulating antidiuretic hormone level IAGP N RGD:5509061 20141003 MGI PMID:15632412 10499 Edn1 endothelin 1 gene MP:0005634 decreased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:15632412 10499 Edn1 endothelin 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16868309 10499 Edn1 endothelin 1 gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20516397 10499 Edn1 endothelin 1 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20516397 10499 Edn1 endothelin 1 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:15314687 10499 Edn1 endothelin 1 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:8152482 10499 Edn1 endothelin 1 gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:8152482 10499 Edn1 endothelin 1 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:7615798 10499 Edn1 endothelin 1 gene MP:0008055 increased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:15632412 10499 Edn1 endothelin 1 gene MP:0009524 absent submandibular gland IAGP N RGD:5509061 20150101 MGI PMID:8152482 10499 Edn1 endothelin 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15632412 10499 Edn1 endothelin 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:7615798 10499 Edn1 endothelin 1 gene MP:0010486 absent right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:7615798 10499 Edn1 endothelin 1 gene MP:0010543 aorta tubular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7615798 10499 Edn1 endothelin 1 gene MP:0010544 interrupted aorta IAGP N RGD:5509061 20141003 MGI PMID:7615798 10499 Edn1 endothelin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20516397 10499 Edn1 endothelin 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8152482 10499 Edn1 endothelin 1 gene MP:0030427 abnormal neck muscle morphology IAGP N RGD:5509061 20221103 MGI PMID:8152482 10505 Ednrb endothelin receptor type B gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20150618 MGI PMID:6049665 10505 Ednrb endothelin receptor type B gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:11773966 10505 Ednrb endothelin receptor type B gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:11773966 10505 Ednrb endothelin receptor type B gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:11773966 10505 Ednrb endothelin receptor type B gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20150618 MGI PMID:6049665 10505 Ednrb endothelin receptor type B gene MP:0000163 abnormal cartilage morphology IEA N RGD:5509061 20111116 MGI 10505 Ednrb endothelin receptor type B gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:19391113 10505 Ednrb endothelin receptor type B gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17693063 10505 Ednrb endothelin receptor type B gene MP:0000373 belly spot IEA N RGD:5509061 20141003 MGI 10505 Ednrb endothelin receptor type B gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20190110 MGI PMID:27134165 10505 Ednrb endothelin receptor type B gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20141003 MGI PMID:17693063 10505 Ednrb endothelin receptor type B gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:19391113 10505 Ednrb endothelin receptor type B gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20150319 MGI PMID:24945437 10505 Ednrb endothelin receptor type B gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20150319 MGI PMID:24945437 10505 Ednrb endothelin receptor type B gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20170525 MGI PMID:26061883 10505 Ednrb endothelin receptor type B gene MP:0000692 small spleen IAGP N RGD:5509061 20170525 MGI PMID:26061883 10505 Ednrb endothelin receptor type B gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20170525 MGI PMID:26061883 10505 Ednrb endothelin receptor type B gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20150618 MGI PMID:5917257 10505 Ednrb endothelin receptor type B gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10591209 10505 Ednrb endothelin receptor type B gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20150618 MGI PMID:5917257 10505 Ednrb endothelin receptor type B gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:14729956 10505 Ednrb endothelin receptor type B gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:14729956 10505 Ednrb endothelin receptor type B gene MP:0001265 decreased body size IAGP N RGD:5509061 20161103 MGI PMID:26240367 10505 Ednrb endothelin receptor type B gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:18693272 10505 Ednrb endothelin receptor type B gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:20048069 10505 Ednrb endothelin receptor type B gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:13943454 10505 Ednrb endothelin receptor type B gene MP:0001574 abnormal oxygen level IAGP N RGD:5509061 20161103 MGI PMID:26240367 10505 Ednrb endothelin receptor type B gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:19391113 10505 Ednrb endothelin receptor type B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8001159 10505 Ednrb endothelin receptor type B gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20170525 MGI PMID:26061883 10505 Ednrb endothelin receptor type B gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:14729956 10505 Ednrb endothelin receptor type B gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:19391113 10505 Ednrb endothelin receptor type B gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:11773966 10505 Ednrb endothelin receptor type B gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11773966 10505 Ednrb endothelin receptor type B gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:5917257 10505 Ednrb endothelin receptor type B gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8001159 10505 Ednrb endothelin receptor type B gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20150618 MGI PMID:8041763 10505 Ednrb endothelin receptor type B gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20161103 MGI PMID:26240367 10505 Ednrb endothelin receptor type B gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20190110 MGI PMID:27134165 10505 Ednrb endothelin receptor type B gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9449665 10505 Ednrb endothelin receptor type B gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:5917257 10505 Ednrb endothelin receptor type B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10591209 10505 Ednrb endothelin receptor type B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11773966 10505 Ednrb endothelin receptor type B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12812796 10505 Ednrb endothelin receptor type B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18693272 10505 Ednrb endothelin receptor type B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8001159 10505 Ednrb endothelin receptor type B gene MP:0002083 premature death IAGP N RGD:5509061 20150618 MGI PMID:5917257 10505 Ednrb endothelin receptor type B gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 10505 Ednrb endothelin receptor type B gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9449665 10505 Ednrb endothelin receptor type B gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:14729956 10505 Ednrb endothelin receptor type B gene MP:0002318 hypercapnia IAGP N RGD:5509061 20141003 MGI PMID:10626068 10505 Ednrb endothelin receptor type B gene MP:0002329 abnormal blood gas level IAGP N RGD:5509061 20141003 MGI PMID:10626068 10505 Ednrb endothelin receptor type B gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20150618 MGI PMID:6049665 10505 Ednrb endothelin receptor type B gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:10591209 10505 Ednrb endothelin receptor type B gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:11773966 10505 Ednrb endothelin receptor type B gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:12812796 10505 Ednrb endothelin receptor type B gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:13800713 10505 Ednrb endothelin receptor type B gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:2304907 10505 Ednrb endothelin receptor type B gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:5917257 10505 Ednrb endothelin receptor type B gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:9371807 10505 Ednrb endothelin receptor type B gene MP:0002731 megacolon IAGP N RGD:5509061 20161103 MGI PMID:26240367 10505 Ednrb endothelin receptor type B gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:24043815 10505 Ednrb endothelin receptor type B gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16868309 10505 Ednrb endothelin receptor type B gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:19391113 10505 Ednrb endothelin receptor type B gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20141003 MGI PMID:18693272 10505 Ednrb endothelin receptor type B gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20141003 MGI PMID:8001159 10505 Ednrb endothelin receptor type B gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:12644183 10505 Ednrb endothelin receptor type B gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:16801484 10505 Ednrb endothelin receptor type B gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:17246828 10505 Ednrb endothelin receptor type B gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:18693272 10505 Ednrb endothelin receptor type B gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:2304907 10505 Ednrb endothelin receptor type B gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:5713933 10505 Ednrb endothelin receptor type B gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:8001159 10505 Ednrb endothelin receptor type B gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:8138159 10505 Ednrb endothelin receptor type B gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:9371807 10505 Ednrb endothelin receptor type B gene MP:0002938 white spotting IAGP N RGD:5509061 20161103 MGI PMID:26240367 10505 Ednrb endothelin receptor type B gene MP:0002939 head spot IEA N RGD:5509061 20141003 MGI 10505 Ednrb endothelin receptor type B gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:11773966 10505 Ednrb endothelin receptor type B gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:17246828 10505 Ednrb endothelin receptor type B gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:17246842 10505 Ednrb endothelin receptor type B gene MP:0003027 abnormal blood pH regulation IAGP N RGD:5509061 20161103 MGI PMID:26240367 10505 Ednrb endothelin receptor type B gene MP:0003032 hypocapnia IAGP N RGD:5509061 20161103 MGI PMID:26240367 10505 Ednrb endothelin receptor type B gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:10496965 10505 Ednrb endothelin receptor type B gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:12812796 10505 Ednrb endothelin receptor type B gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:5713933 10505 Ednrb endothelin receptor type B gene MP:0003154 abnormal soft palate morphology IAGP N RGD:5509061 20141003 MGI PMID:17693063 10505 Ednrb endothelin receptor type B gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19391113 10505 Ednrb endothelin receptor type B gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:16801484 10505 Ednrb endothelin receptor type B gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:8001159 10505 Ednrb endothelin receptor type B gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20170525 MGI PMID:26061883 10505 Ednrb endothelin receptor type B gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20150618 MGI PMID:6049665 10505 Ednrb endothelin receptor type B gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20161103 MGI PMID:26240367 10505 Ednrb endothelin receptor type B gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:16868309 10505 Ednrb endothelin receptor type B gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 10505 Ednrb endothelin receptor type B gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16801484 10505 Ednrb endothelin receptor type B gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:19391113 10505 Ednrb endothelin receptor type B gene MP:0004302 abnormal Deiters cell morphology IAGP N RGD:5509061 20150618 MGI PMID:6049665 10505 Ednrb endothelin receptor type B gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11773966 10505 Ednrb endothelin receptor type B gene MP:0004364 thin stria vascularis IAGP N RGD:5509061 20141003 MGI PMID:11773966 10505 Ednrb endothelin receptor type B gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8001159 10505 Ednrb endothelin receptor type B gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20190110 MGI PMID:27134165 10505 Ednrb endothelin receptor type B gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20161103 MGI PMID:26240367 10505 Ednrb endothelin receptor type B gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:17693063 10505 Ednrb endothelin receptor type B gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20150319 MGI PMID:24945437 10505 Ednrb endothelin receptor type B gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10626068 10505 Ednrb endothelin receptor type B gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20161103 MGI PMID:26240367 10505 Ednrb endothelin receptor type B gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20170525 MGI PMID:26061883 10505 Ednrb endothelin receptor type B gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170525 MGI PMID:26061883 10505 Ednrb endothelin receptor type B gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:10626068 10505 Ednrb endothelin receptor type B gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:10496965 10505 Ednrb endothelin receptor type B gene MP:0005100 abnormal choroid pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8001159 10505 Ednrb endothelin receptor type B gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:8001159 10505 Ednrb endothelin receptor type B gene MP:0005150 cachexia IAGP N RGD:5509061 20161103 MGI PMID:26240367 10505 Ednrb endothelin receptor type B gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:17693063 10505 Ednrb endothelin receptor type B gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10591209 10505 Ednrb endothelin receptor type B gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12812796 10505 Ednrb endothelin receptor type B gene MP:0005174 abnormal tail pigmentation IEA N RGD:5509061 20111116 MGI 10505 Ednrb endothelin receptor type B gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:19391113 10505 Ednrb endothelin receptor type B gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:9449665 10505 Ednrb endothelin receptor type B gene MP:0005508 abnormal skeleton morphology IEA N RGD:5509061 20111116 MGI 10505 Ednrb endothelin receptor type B gene MP:0005583 decreased renin activity IAGP N RGD:5509061 20141003 MGI PMID:16868309 10505 Ednrb endothelin receptor type B gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:16801484 10505 Ednrb endothelin receptor type B gene MP:0005600 increased heart ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:26240367 10505 Ednrb endothelin receptor type B gene MP:0006010 absent strial intermediate cells IAGP N RGD:5509061 20141003 MGI PMID:11773966 10505 Ednrb endothelin receptor type B gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16868309 10505 Ednrb endothelin receptor type B gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16868309 10505 Ednrb endothelin receptor type B gene MP:0006274 abnormal urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:16868309 10505 Ednrb endothelin receptor type B gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20170525 MGI PMID:26061883 10505 Ednrb endothelin receptor type B gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20170525 MGI PMID:26061883 10505 Ednrb endothelin receptor type B gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20170525 MGI PMID:26061883 10505 Ednrb endothelin receptor type B gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17693063 10505 Ednrb endothelin receptor type B gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20170525 MGI PMID:26061883 10505 Ednrb endothelin receptor type B gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20170525 MGI PMID:26061883 10505 Ednrb endothelin receptor type B gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18693272 10505 Ednrb endothelin receptor type B gene MP:0008569 lethality at weaning IEA N RGD:5509061 20141225 MGI 10505 Ednrb endothelin receptor type B gene MP:0008732 reduced hair shaft melanin granule number IAGP N RGD:5509061 20190110 MGI PMID:27134165 10505 Ednrb endothelin receptor type B gene MP:0008786 abnormal hindgut morphology IAGP N RGD:5509061 20150618 MGI PMID:4772386 10505 Ednrb endothelin receptor type B gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20170525 MGI PMID:26061883 10505 Ednrb endothelin receptor type B gene MP:0009379 abnormal foot pigmentation IEA N RGD:5509061 20111116 MGI 10505 Ednrb endothelin receptor type B gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20190110 MGI PMID:27134165 10505 Ednrb endothelin receptor type B gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16801484 10505 Ednrb endothelin receptor type B gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16868309 10505 Ednrb endothelin receptor type B gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20141003 MGI PMID:17693063 10505 Ednrb endothelin receptor type B gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141003 MGI PMID:17693063 10505 Ednrb endothelin receptor type B gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:17693063 10505 Ednrb endothelin receptor type B gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:17693063 10505 Ednrb endothelin receptor type B gene MP:0009891 abnormal palate bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17693063 10505 Ednrb endothelin receptor type B gene MP:0009898 maxillary shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17693063 10505 Ednrb endothelin receptor type B gene MP:0010016 variable depigmentation IAGP N RGD:5509061 20141003 MGI PMID:8001159 10505 Ednrb endothelin receptor type B gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20150319 MGI PMID:24945437 10505 Ednrb endothelin receptor type B gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20048069 10505 Ednrb endothelin receptor type B gene MP:0010741 abnormal melanocyte proliferation IAGP N RGD:5509061 20150618 MGI PMID:8041763 10505 Ednrb endothelin receptor type B gene MP:0010741 abnormal melanocyte proliferation IAGP N RGD:5509061 20190110 MGI PMID:27134165 10505 Ednrb endothelin receptor type B gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20161103 MGI PMID:26240367 10505 Ednrb endothelin receptor type B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16801484 10505 Ednrb endothelin receptor type B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8138159 10505 Ednrb endothelin receptor type B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9371807 10505 Ednrb endothelin receptor type B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2304907 10505 Ednrb endothelin receptor type B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8138159 10505 Ednrb endothelin receptor type B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9371807 10505 Ednrb endothelin receptor type B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19391113 10505 Ednrb endothelin receptor type B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8138159 10505 Ednrb endothelin receptor type B gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1352884 10505 Ednrb endothelin receptor type B gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8138159 10505 Ednrb endothelin receptor type B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19391113 10505 Ednrb endothelin receptor type B gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19391113 10505 Ednrb endothelin receptor type B gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19391113 10505 Ednrb endothelin receptor type B gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19391113 10505 Ednrb endothelin receptor type B gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2304907 10505 Ednrb endothelin receptor type B gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8138159 10505 Ednrb endothelin receptor type B gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20150618 MGI PMID:5917257 10505 Ednrb endothelin receptor type B gene MP:0011494 abnormal pigmentation pattern IAGP N RGD:5509061 20150618 MGI PMID:5917257 10505 Ednrb endothelin receptor type B gene MP:0011494 abnormal pigmentation pattern IAGP N RGD:5509061 20150618 MGI PMID:8041763 10505 Ednrb endothelin receptor type B gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20190110 MGI PMID:27134165 10505 Ednrb endothelin receptor type B gene MP:0013006 abnormal enteric neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:18693272 10505 Ednrb endothelin receptor type B gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20161103 MGI PMID:26240367 10505 Ednrb endothelin receptor type B gene MP:0013701 abnormal mature B cell number IAGP N RGD:5509061 20170525 MGI PMID:26061883 10505 Ednrb endothelin receptor type B gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:24945437 10505 Ednrb endothelin receptor type B gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:20048069 10505 Ednrb endothelin receptor type B gene MP:0014484 decreased feces water content IAGP N RGD:5509061 20240704 MGI PMID:24945437 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20150129 MGI PMID:24582807 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20150129 MGI PMID:24582807 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20200924 MGI PMID:30838762 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20150129 MGI PMID:24582807 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20160428 MGI PMID:25755286 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20150129 MGI PMID:24582807 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20150129 MGI PMID:24582807 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20472894 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20150129 MGI PMID:24582807 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20160428 MGI PMID:25670349 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20150129 MGI PMID:24582807 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20150129 MGI PMID:24582807 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0009083 uterus hypertrophy IAGP N RGD:5509061 20220407 MGI PMID:24582807 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0011120 increased primordial ovarian follicle number IAGP N RGD:5509061 20150129 MGI PMID:24582807 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0011124 increased primary ovarian follicle number IAGP N RGD:5509061 20150129 MGI PMID:24582807 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0011128 increased tertiary ovarian follicle number IAGP N RGD:5509061 20150129 MGI PMID:24582807 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0013475 delayed reproductive senescence IAGP N RGD:5509061 20220616 MGI PMID:24582807 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:24582807 10506 Eef2k eukaryotic elongation factor-2 kinase gene MP:0031421 increased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:24582807 10508 Efnb1 ephrin B1 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:15037550 10508 Efnb1 ephrin B1 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:19515977 10508 Efnb1 ephrin B1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16968134 10508 Efnb1 ephrin B1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:15037550 10508 Efnb1 ephrin B1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:19515977 10508 Efnb1 ephrin B1 gene MP:0000155 asymmetric rib joints IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:15037550 10508 Efnb1 ephrin B1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19515977 10508 Efnb1 ephrin B1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0000618 small salivary gland IAGP N RGD:5509061 20141003 MGI PMID:17223098 10508 Efnb1 ephrin B1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:19515977 10508 Efnb1 ephrin B1 gene MP:0001061 abnormal oculomotor nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15037550 10508 Efnb1 ephrin B1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:15037550 10508 Efnb1 ephrin B1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:16968134 10508 Efnb1 ephrin B1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:19515977 10508 Efnb1 ephrin B1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17223098 10508 Efnb1 ephrin B1 gene MP:0003840 abnormal coronal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:16968134 10508 Efnb1 ephrin B1 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0004378 frontal bone foramen IAGP N RGD:5509061 20141003 MGI PMID:16968134 10508 Efnb1 ephrin B1 gene MP:0004378 frontal bone foramen IAGP N RGD:5509061 20141003 MGI PMID:19515977 10508 Efnb1 ephrin B1 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:21847105 10508 Efnb1 ephrin B1 gene MP:0006322 abnormal perichondrium morphology IAGP N RGD:5509061 20141003 MGI PMID:15037550 10508 Efnb1 ephrin B1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:17223098 10508 Efnb1 ephrin B1 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0009882 absent palatal shelf IAGP N RGD:5509061 20141003 MGI PMID:15037550 10508 Efnb1 ephrin B1 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:15037550 10508 Efnb1 ephrin B1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15037550 10508 Efnb1 ephrin B1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:19515977 10508 Efnb1 ephrin B1 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21976681 10508 Efnb1 ephrin B1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15037550 10508 Efnb1 ephrin B1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12919674 10508 Efnb1 ephrin B1 gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:15037550 10508 Efnb1 ephrin B1 gene MP:0012757 abnormal cranial neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:15037550 10508 Efnb1 ephrin B1 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:21976681 10509 Efnb3 ephrin B3 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12649481 10509 Efnb3 ephrin B3 gene MP:0001393 ataxia IEA N RGD:5509061 20150910 MGI 10509 Efnb3 ephrin B3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11182083 10509 Efnb3 ephrin B3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11182083 10509 Efnb3 ephrin B3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11297511 10509 Efnb3 ephrin B3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12649481 10509 Efnb3 ephrin B3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19182796 10509 Efnb3 ephrin B3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:14699416 10509 Efnb3 ephrin B3 gene MP:0001523 impaired righting response IEA N RGD:5509061 20150910 MGI 10509 Efnb3 ephrin B3 gene MP:0001524 impaired limb coordination IEA N RGD:5509061 20141003 MGI 10509 Efnb3 ephrin B3 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:14699416 10509 Efnb3 ephrin B3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11182083 10509 Efnb3 ephrin B3 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:11182083 10509 Efnb3 ephrin B3 gene MP:0002862 abnormal righting response IEA N RGD:5509061 20141003 MGI 10509 Efnb3 ephrin B3 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:11182083 10509 Efnb3 ephrin B3 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:11297511 10509 Efnb3 ephrin B3 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:12649481 10509 Efnb3 ephrin B3 gene MP:0003880 abnormal central pattern generator function IAGP N RGD:5509061 20141003 MGI PMID:12649481 10509 Efnb3 ephrin B3 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19182796 10509 Efnb3 ephrin B3 gene MP:0008960 abnormal axon pruning IAGP N RGD:5509061 20141003 MGI PMID:19182796 10509 Efnb3 ephrin B3 gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20150910 MGI 10510 Egf epidermal growth factor gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:10331984 10510 Egf epidermal growth factor gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:15456865 10510 Egf epidermal growth factor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:10331984 10510 Egf epidermal growth factor gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:11438495 10510 Egf epidermal growth factor gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:10331984 10510 Egf epidermal growth factor gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:10331984 10510 Egf epidermal growth factor gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:10331984 10510 Egf epidermal growth factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11438495 10510 Egf epidermal growth factor gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10331984 10510 Egf epidermal growth factor gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:10331984 10510 Egf epidermal growth factor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10331984 10510 Egf epidermal growth factor gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:10331984 10510 Egf epidermal growth factor gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15456865 10510 Egf epidermal growth factor gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:10331984 10510 Egf epidermal growth factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10331984 10510 Egf epidermal growth factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10331984 10510 Egf epidermal growth factor gene MP:0002580 duodenal lesions IAGP N RGD:5509061 20141003 MGI PMID:11438495 10510 Egf epidermal growth factor gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:11438495 10510 Egf epidermal growth factor gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11438495 10510 Egf epidermal growth factor gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:11438495 10510 Egf epidermal growth factor gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:10331984 10510 Egf epidermal growth factor gene MP:0013716 hypolactation IAGP N RGD:5509061 20150402 MGI PMID:10331984 10511 Egfr epidermal growth factor receptor gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:10319864 10511 Egfr epidermal growth factor receptor gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10319864 10511 Egfr epidermal growth factor receptor gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20141003 MGI 10511 Egfr epidermal growth factor receptor gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20170810 MGI PMID:25997932 10511 Egfr epidermal growth factor receptor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170810 MGI PMID:25997932 10511 Egfr epidermal growth factor receptor gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:18772111 10511 Egfr epidermal growth factor receptor gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18830272 10511 Egfr epidermal growth factor receptor gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:15020428 10511 Egfr epidermal growth factor receptor gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0000384 distorted hair follicle pattern IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0000396 increased curvature of hairs IAGP N RGD:5509061 20141003 MGI PMID:5142632 10511 Egfr epidermal growth factor receptor gene MP:0000399 increased curvature of guard hairs IEA N RGD:5509061 20111116 MGI 10511 Egfr epidermal growth factor receptor gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:11929848 10511 Egfr epidermal growth factor receptor gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:12533510 10511 Egfr epidermal growth factor receptor gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:15020428 10511 Egfr epidermal growth factor receptor gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:19115345 10511 Egfr epidermal growth factor receptor gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:5142632 10511 Egfr epidermal growth factor receptor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0000446 long snout IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0000448 pointed snout IAGP N RGD:5509061 20141003 MGI PMID:10319864 10511 Egfr epidermal growth factor receptor gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20170921 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 10511 Egfr epidermal growth factor receptor gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:12533510 10511 Egfr epidermal growth factor receptor gene MP:0000583 long toenails IAGP N RGD:5509061 20141003 MGI PMID:12533510 10511 Egfr epidermal growth factor receptor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:7533293 10511 Egfr epidermal growth factor receptor gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0000763 abnormal filiform papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18830272 10511 Egfr epidermal growth factor receptor gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:18830272 10511 Egfr epidermal growth factor receptor gene MP:0001142 abnormal vagina orifice morphology IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0001194 dermatitis IAGP N RGD:5509061 20181122 MGI PMID:25902485 10511 Egfr epidermal growth factor receptor gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0001195 flaky skin IAGP N RGD:5509061 20170309 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0001200 thick skin IEA N RGD:5509061 20160616 MGI 10511 Egfr epidermal growth factor receptor gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18772111 10511 Egfr epidermal growth factor receptor gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20181122 MGI PMID:25902485 10511 Egfr epidermal growth factor receptor gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:12533510 10511 Egfr epidermal growth factor receptor gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:18772111 10511 Egfr epidermal growth factor receptor gene MP:0001221 epidermal atrophy IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21041656 10511 Egfr epidermal growth factor receptor gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:11929848 10511 Egfr epidermal growth factor receptor gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:15020428 10511 Egfr epidermal growth factor receptor gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0001279 wavy vibrissae IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0001280 loss of vibrissae IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0001282 short vibrissae IEA N RGD:5509061 20111116 MGI 10511 Egfr epidermal growth factor receptor gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15020428 10511 Egfr epidermal growth factor receptor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:9030684 10511 Egfr epidermal growth factor receptor gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:11929848 10511 Egfr epidermal growth factor receptor gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15020428 10511 Egfr epidermal growth factor receptor gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:9030684 10511 Egfr epidermal growth factor receptor gene MP:0001304 cataract IEA N RGD:5509061 20141003 MGI 10511 Egfr epidermal growth factor receptor gene MP:0001306 small lens IAGP N RGD:5509061 20160310 MGI PMID:9030684 10511 Egfr epidermal growth factor receptor gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20141003 MGI PMID:9030684 10511 Egfr epidermal growth factor receptor gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 10511 Egfr epidermal growth factor receptor gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:15020428 10511 Egfr epidermal growth factor receptor gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:9030684 10511 Egfr epidermal growth factor receptor gene MP:0001316 cornea scarring IAGP N RGD:5509061 20141003 MGI PMID:11929848 10511 Egfr epidermal growth factor receptor gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 10511 Egfr epidermal growth factor receptor gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:15020428 10511 Egfr epidermal growth factor receptor gene MP:0001341 absent eyelids IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0001511 disheveled coat IEA N RGD:5509061 20160616 MGI 10511 Egfr epidermal growth factor receptor gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19115345 10511 Egfr epidermal growth factor receptor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15020428 10511 Egfr epidermal growth factor receptor gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19115345 10511 Egfr epidermal growth factor receptor gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:19115345 10511 Egfr epidermal growth factor receptor gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:7533293 10511 Egfr epidermal growth factor receptor gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:10821760 10511 Egfr epidermal growth factor receptor gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:21119595 10511 Egfr epidermal growth factor receptor gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15652750 10511 Egfr epidermal growth factor receptor gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:16648858 10511 Egfr epidermal growth factor receptor gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20181122 MGI PMID:25902485 10511 Egfr epidermal growth factor receptor gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20141003 MGI PMID:11929848 10511 Egfr epidermal growth factor receptor gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20141003 MGI PMID:8125255 10511 Egfr epidermal growth factor receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18772111 10511 Egfr epidermal growth factor receptor gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11929848 10511 Egfr epidermal growth factor receptor gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:18772111 10511 Egfr epidermal growth factor receptor gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 10511 Egfr epidermal growth factor receptor gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:11929848 10511 Egfr epidermal growth factor receptor gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:8125255 10511 Egfr epidermal growth factor receptor gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15456865 10511 Egfr epidermal growth factor receptor gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0002268 abnormal terminal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0002497 increased IgE level IAGP N RGD:5509061 20181122 MGI PMID:25902485 10511 Egfr epidermal growth factor receptor gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20170810 MGI PMID:25997932 10511 Egfr epidermal growth factor receptor gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20170810 MGI PMID:25997932 10511 Egfr epidermal growth factor receptor gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20181122 MGI PMID:25902485 10511 Egfr epidermal growth factor receptor gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 10511 Egfr epidermal growth factor receptor gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20170810 MGI PMID:25997932 10511 Egfr epidermal growth factor receptor gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21119595 10511 Egfr epidermal growth factor receptor gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21119595 10511 Egfr epidermal growth factor receptor gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0003812 abnormal hair medulla IAGP N RGD:5509061 20141003 MGI PMID:5142632 10511 Egfr epidermal growth factor receptor gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0003820 increased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0003853 dry skin IAGP N RGD:5509061 20170309 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20170810 MGI PMID:25997932 10511 Egfr epidermal growth factor receptor gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:10821760 10511 Egfr epidermal growth factor receptor gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19115345 10511 Egfr epidermal growth factor receptor gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15020428 10511 Egfr epidermal growth factor receptor gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 10511 Egfr epidermal growth factor receptor gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 10511 Egfr epidermal growth factor receptor gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10821760 10511 Egfr epidermal growth factor receptor gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:10821760 10511 Egfr epidermal growth factor receptor gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20160310 MGI PMID:9030684 10511 Egfr epidermal growth factor receptor gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20170810 MGI PMID:25997932 10511 Egfr epidermal growth factor receptor gene MP:0006026 dilated terminal bronchiole tube IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20170810 MGI PMID:25997932 10511 Egfr epidermal growth factor receptor gene MP:0006116 calcified aortic valve IAGP N RGD:5509061 20170810 MGI PMID:25997932 10511 Egfr epidermal growth factor receptor gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20170810 MGI PMID:25997932 10511 Egfr epidermal growth factor receptor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0006257 abnormal fungiform papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0006265 increased pulse pressure IAGP N RGD:5509061 20170810 MGI PMID:25997932 10511 Egfr epidermal growth factor receptor gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20181122 MGI PMID:25902485 10511 Egfr epidermal growth factor receptor gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20181122 MGI PMID:25902485 10511 Egfr epidermal growth factor receptor gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17940036 10511 Egfr epidermal growth factor receptor gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17940036 10511 Egfr epidermal growth factor receptor gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18772111 10511 Egfr epidermal growth factor receptor gene MP:0008816 petechiae IAGP N RGD:5509061 20170309 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0008817 hematoma IAGP N RGD:5509061 20170309 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0008862 asymmetric snout IAGP N RGD:5509061 20171019 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0008899 plush coat IAGP N RGD:5509061 20141003 MGI PMID:15020428 10511 Egfr epidermal growth factor receptor gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:10821760 10511 Egfr epidermal growth factor receptor gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:15020428 10511 Egfr epidermal growth factor receptor gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20141225 MGI PMID:15020428 10511 Egfr epidermal growth factor receptor gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17940036 10511 Egfr epidermal growth factor receptor gene MP:0009801 abnormal hair cortex keratinization IAGP N RGD:5509061 20141003 MGI PMID:5142632 10511 Egfr epidermal growth factor receptor gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20170309 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0010179 rough coat IEA N RGD:5509061 20160616 MGI 10511 Egfr epidermal growth factor receptor gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20181122 MGI PMID:25902485 10511 Egfr epidermal growth factor receptor gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21119595 10511 Egfr epidermal growth factor receptor gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0010570 prolonged ST segment IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20170810 MGI PMID:25997932 10511 Egfr epidermal growth factor receptor gene MP:0010591 enlarged aortic valve IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20240125 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0010890 decreased alveolar lamellar body number IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0010897 abnormal bronchiole epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0010898 abnormal pulmonary alveolus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0010911 abnormal pulmonary acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:9205141 10511 Egfr epidermal growth factor receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18772111 10511 Egfr epidermal growth factor receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10411909 10511 Egfr epidermal growth factor receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0011092 embryonic lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 10511 Egfr epidermal growth factor receptor gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15020428 10511 Egfr epidermal growth factor receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11929848 10511 Egfr epidermal growth factor receptor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7630400 10511 Egfr epidermal growth factor receptor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9030684 10511 Egfr epidermal growth factor receptor gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141003 MGI PMID:9030684 10511 Egfr epidermal growth factor receptor gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:9030684 10511 Egfr epidermal growth factor receptor gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:15020428 10511 Egfr epidermal growth factor receptor gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0011926 abnormal heart valve physiology IAGP N RGD:5509061 20170810 MGI PMID:25997932 10511 Egfr epidermal growth factor receptor gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20170810 MGI PMID:25997932 10511 Egfr epidermal growth factor receptor gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20160310 MGI PMID:9030684 10511 Egfr epidermal growth factor receptor gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:7618084 10511 Egfr epidermal growth factor receptor gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:7618085 10511 Egfr epidermal growth factor receptor gene MP:0013542 abnormal submandibular gland branching morphogenesis IAGP N RGD:5509061 20150326 MGI PMID:10521784 10511 Egfr epidermal growth factor receptor gene MP:0014107 premature chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:12925580 10511 Egfr epidermal growth factor receptor gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:28404843 10511 Egfr epidermal growth factor receptor gene MP:0030026 small Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:10319864 10511 Egfr epidermal growth factor receptor gene MP:0030191 narrow snout IAGP N RGD:5509061 20171019 MGI PMID:15366372 10511 Egfr epidermal growth factor receptor gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:28404843 10511 Egfr epidermal growth factor receptor gene MP:0031324 delayed liver regeneration IAGP N RGD:5509061 20220106 MGI PMID:17940036 10511 Egfr epidermal growth factor receptor gene MP:0031580 enlarged semilunar valve IAGP N RGD:5509061 20240125 MGI PMID:10700187 10511 Egfr epidermal growth factor receptor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:25997932 10511 Egfr epidermal growth factor receptor gene MP:0031634 decreased heart right ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:25997932 10512 Egr1 early growth response 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:10792003 10512 Egr1 early growth response 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10792003 10512 Egr1 early growth response 1 gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17420284 10512 Egr1 early growth response 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:17420284 10512 Egr1 early growth response 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17420284 10512 Egr1 early growth response 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:15940638 10512 Egr1 early growth response 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:17916644 10512 Egr1 early growth response 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:8703054 10512 Egr1 early growth response 1 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:8703054 10512 Egr1 early growth response 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:19679873 10512 Egr1 early growth response 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 10512 Egr1 early growth response 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:17197510 10512 Egr1 early growth response 1 gene MP:0001573 abnormal circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:15940638 10512 Egr1 early growth response 1 gene MP:0001573 abnormal circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17916644 10512 Egr1 early growth response 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17420284 10512 Egr1 early growth response 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20170105 MGI 10512 Egr1 early growth response 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17420284 10512 Egr1 early growth response 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0001746 abnormal pituitary secretion IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15940638 10512 Egr1 early growth response 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:17916644 10512 Egr1 early growth response 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:15289506 10512 Egr1 early growth response 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:19679873 10512 Egr1 early growth response 1 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:8703054 10512 Egr1 early growth response 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11739581 10512 Egr1 early growth response 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8703054 10512 Egr1 early growth response 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20141003 MGI PMID:8703054 10512 Egr1 early growth response 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17420284 10512 Egr1 early growth response 1 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:15958557 10512 Egr1 early growth response 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11135623 10512 Egr1 early growth response 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11135623 10512 Egr1 early growth response 1 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:17197510 10512 Egr1 early growth response 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:17197510 10512 Egr1 early growth response 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:15289506 10512 Egr1 early growth response 1 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0002697 abnormal eye size IAGP N RGD:5509061 20141003 MGI PMID:17197510 10512 Egr1 early growth response 1 gene MP:0002764 short tibia IEA N RGD:5509061 20170105 MGI 10512 Egr1 early growth response 1 gene MP:0002774 small prostate gland IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0002801 abnormal long-term object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:14622575 10512 Egr1 early growth response 1 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:19679873 10512 Egr1 early growth response 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10710348 10512 Egr1 early growth response 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17420284 10512 Egr1 early growth response 1 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20170105 MGI 10512 Egr1 early growth response 1 gene MP:0003426 pulmonary interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19679873 10512 Egr1 early growth response 1 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20170105 MGI 10512 Egr1 early growth response 1 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18208539 10512 Egr1 early growth response 1 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20170105 MGI 10512 Egr1 early growth response 1 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20170105 MGI 10512 Egr1 early growth response 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 10512 Egr1 early growth response 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:15265859 10512 Egr1 early growth response 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17420284 10512 Egr1 early growth response 1 gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:15265859 10512 Egr1 early growth response 1 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18397757 10512 Egr1 early growth response 1 gene MP:0004848 abnormal liver size IAGP N RGD:5509061 20141003 MGI PMID:15940638 10512 Egr1 early growth response 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:10710348 10512 Egr1 early growth response 1 gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:8703054 10512 Egr1 early growth response 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17420284 10512 Egr1 early growth response 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:9819371 10512 Egr1 early growth response 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17420284 10512 Egr1 early growth response 1 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:17420284 10512 Egr1 early growth response 1 gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:8703054 10512 Egr1 early growth response 1 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:18208539 10512 Egr1 early growth response 1 gene MP:0005184 abnormal circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:8703054 10512 Egr1 early growth response 1 gene MP:0005340 abnormal susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:14670837 10512 Egr1 early growth response 1 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:15265859 10512 Egr1 early growth response 1 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11135623 10512 Egr1 early growth response 1 gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15289506 10512 Egr1 early growth response 1 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19679873 10512 Egr1 early growth response 1 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:18208539 10512 Egr1 early growth response 1 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20170105 MGI 10512 Egr1 early growth response 1 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17420284 10512 Egr1 early growth response 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20201231 MGI 10512 Egr1 early growth response 1 gene MP:0008329 decreased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0008365 adenohypophysis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0008552 abnormal circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17916644 10512 Egr1 early growth response 1 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15940638 10512 Egr1 early growth response 1 gene MP:0008869 anovulation IAGP N RGD:5509061 20220804 MGI PMID:9440815 10512 Egr1 early growth response 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15940638 10512 Egr1 early growth response 1 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20161027 MGI PMID:8703054 10512 Egr1 early growth response 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15940638 10512 Egr1 early growth response 1 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:11135623 10512 Egr1 early growth response 1 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:15958557 10512 Egr1 early growth response 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20170105 MGI 10512 Egr1 early growth response 1 gene MP:0012432 decreased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11135623 10512 Egr1 early growth response 1 gene MP:0013599 Leydig cell atrophy IAGP N RGD:5509061 20150319 MGI PMID:8703054 10512 Egr1 early growth response 1 gene MP:0031213 increased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:17197510 10516 Cela1 chymotrypsin-like elastase family, member 1 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20190926 MGI PMID:29420065 10516 Cela1 chymotrypsin-like elastase family, member 1 gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20190926 MGI PMID:29420065 10516 Cela1 chymotrypsin-like elastase family, member 1 gene MP:0011044 increased lung elastance IAGP N RGD:5509061 20190926 MGI PMID:29420065 10516 Cela1 chymotrypsin-like elastase family, member 1 gene MP:0011163 increased wet-to-dry lung weight ratio IAGP N RGD:5509061 20190926 MGI PMID:29420065 10518 Elk1 ELK1, member of ETS oncogene family gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14673163 10518 Elk1 ELK1, member of ETS oncogene family gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20210128 MGI 10518 Elk1 ELK1, member of ETS oncogene family gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:14994271 10518 Elk1 ELK1, member of ETS oncogene family gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 10519 Emd emerin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16507906 10519 Emd emerin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20171116 MGI PMID:25274778 10519 Emd emerin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16507906 10519 Emd emerin gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20171116 MGI PMID:25274778 10519 Emd emerin gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20230601 MGI 10519 Emd emerin gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 10519 Emd emerin gene MP:0002833 increased heart weight IAGP N RGD:5509061 20171116 MGI PMID:25274778 10519 Emd emerin gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20141003 MGI PMID:16403804 10519 Emd emerin gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16507906 10519 Emd emerin gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:16507906 10519 Emd emerin gene MP:0003960 increased lean body mass IEA N RGD:5509061 20240523 MGI 10519 Emd emerin gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20171116 MGI PMID:25274778 10519 Emd emerin gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20171116 MGI PMID:25274778 10519 Emd emerin gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20171116 MGI PMID:25274778 10519 Emd emerin gene MP:0006321 increased myocardial fiber number IAGP N RGD:5509061 20171116 MGI PMID:25274778 10519 Emd emerin gene MP:0009455 enhanced cued conditioning behavior IEA N RGD:5509061 20230601 MGI 10519 Emd emerin gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20171116 MGI PMID:25274778 10519 Emd emerin gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:25274778 10519 Emd emerin gene MP:0031634 decreased heart right ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:25274778 10520 Emp1 epithelial membrane protein 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 10521 Eno1 enolase 1, alpha non-neuron gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9626503 10521 Eno1 enolase 1, alpha non-neuron gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9626503 10521 Eno1 enolase 1, alpha non-neuron gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9626503 10527 Eno2 enolase 2, gamma neuronal gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:18758458 10527 Eno2 enolase 2, gamma neuronal gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:18758458 10527 Eno2 enolase 2, gamma neuronal gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141030 MGI PMID:23487260 10527 Eno2 enolase 2, gamma neuronal gene MP:0001003 abnormal olfactory receptor morphology IAGP N RGD:5509061 20141003 MGI PMID:17989651 10527 Eno2 enolase 2, gamma neuronal gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141030 MGI PMID:23487260 10527 Eno2 enolase 2, gamma neuronal gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141030 MGI PMID:23487260 10527 Eno2 enolase 2, gamma neuronal gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19132103 10527 Eno2 enolase 2, gamma neuronal gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141030 MGI PMID:23487260 10527 Eno2 enolase 2, gamma neuronal gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 10527 Eno2 enolase 2, gamma neuronal gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19132103 10527 Eno2 enolase 2, gamma neuronal gene MP:0001460 abnormal olfactory discrimination memory IAGP N RGD:5509061 20141003 MGI PMID:17989651 10527 Eno2 enolase 2, gamma neuronal gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18758458 10527 Eno2 enolase 2, gamma neuronal gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:17989651 10527 Eno2 enolase 2, gamma neuronal gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:19132103 10527 Eno2 enolase 2, gamma neuronal gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:17989651 10527 Eno2 enolase 2, gamma neuronal gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:19132103 10527 Eno2 enolase 2, gamma neuronal gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19132103 10527 Eno2 enolase 2, gamma neuronal gene MP:0004082 abnormal habenula morphology IAGP N RGD:5509061 20141030 MGI PMID:23487260 10527 Eno2 enolase 2, gamma neuronal gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17989651 10527 Eno2 enolase 2, gamma neuronal gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141030 MGI PMID:23487260 10527 Eno2 enolase 2, gamma neuronal gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:18758458 10527 Eno2 enolase 2, gamma neuronal gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19132103 10527 Eno2 enolase 2, gamma neuronal gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:18758458 10527 Eno2 enolase 2, gamma neuronal gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:18758458 10527 Eno2 enolase 2, gamma neuronal gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141030 MGI PMID:23487260 10527 Eno2 enolase 2, gamma neuronal gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141030 MGI PMID:23487260 10527 Eno2 enolase 2, gamma neuronal gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20151217 MGI PMID:24496082 10527 Eno2 enolase 2, gamma neuronal gene MP:0009756 impaired behavioral response to nicotine IAGP N RGD:5509061 20141030 MGI PMID:23487260 10527 Eno2 enolase 2, gamma neuronal gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20141030 MGI PMID:23487260 10527 Eno2 enolase 2, gamma neuronal gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20141030 MGI PMID:23487260 10527 Eno2 enolase 2, gamma neuronal gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20141030 MGI PMID:23487260 10528 Eno3 enolase 3, beta muscle gene MP:0001513 limb grasping IEA N RGD:5509061 20230601 MGI 10528 Eno3 enolase 3, beta muscle gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230601 MGI 10529 Ephx1 epoxide hydrolase 1, microsomal gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:10446164 10530 Stx2 syntaxin 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18277055 10530 Stx2 syntaxin 2 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18277055 10530 Stx2 syntaxin 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16710473 10530 Stx2 syntaxin 2 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 10530 Stx2 syntaxin 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 10530 Stx2 syntaxin 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16710473 10530 Stx2 syntaxin 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18277055 10530 Stx2 syntaxin 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:16710473 10530 Stx2 syntaxin 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16710473 10530 Stx2 syntaxin 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 10530 Stx2 syntaxin 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16710473 10530 Stx2 syntaxin 2 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 10530 Stx2 syntaxin 2 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:16710473 10530 Stx2 syntaxin 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16710473 10530 Stx2 syntaxin 2 gene MP:0004910 decreased seminal vesicle weight IEA N RGD:5509061 20111116 MGI 10530 Stx2 syntaxin 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:16710473 10530 Stx2 syntaxin 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:18277055 10530 Stx2 syntaxin 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 10530 Stx2 syntaxin 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 10530 Stx2 syntaxin 2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 10530 Stx2 syntaxin 2 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20160526 MGI PMID:16710473 10530 Stx2 syntaxin 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18277055 10530 Stx2 syntaxin 2 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20160526 MGI PMID:16710473 10530 Stx2 syntaxin 2 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20160526 MGI PMID:16710473 10530 Stx2 syntaxin 2 gene MP:0013955 increased colon length IAGP N RGD:5509061 20160304 MGI PMID:16710473 10530 Stx2 syntaxin 2 gene MP:0013957 increased small intestine length IAGP N RGD:5509061 20160526 MGI PMID:16710473 10530 Stx2 syntaxin 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20160526 MGI PMID:16710473 10530 Stx2 syntaxin 2 gene MP:0014081 branched small intestinal villi IAGP N RGD:5509061 20160526 MGI PMID:16710473 10530 Stx2 syntaxin 2 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:18277055 10531 Epo erythropoietin gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20959632 10531 Epo erythropoietin gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20959632 10531 Epo erythropoietin gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:7553874 10531 Epo erythropoietin gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10409505 10531 Epo erythropoietin gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10409505 10531 Epo erythropoietin gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:10409505 10531 Epo erythropoietin gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:7553874 10531 Epo erythropoietin gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:7553874 10531 Epo erythropoietin gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10409505 10531 Epo erythropoietin gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12239150 10531 Epo erythropoietin gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15878311 10531 Epo erythropoietin gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7553874 10531 Epo erythropoietin gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8264149 10531 Epo erythropoietin gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10409505 10531 Epo erythropoietin gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:7553874 10531 Epo erythropoietin gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:10409505 10531 Epo erythropoietin gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:10409505 10531 Epo erythropoietin gene MP:0002319 hyperoxia IAGP N RGD:5509061 20141003 MGI PMID:15878311 10531 Epo erythropoietin gene MP:0002320 hyperventilation IAGP N RGD:5509061 20141003 MGI PMID:15878311 10531 Epo erythropoietin gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12239150 10531 Epo erythropoietin gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20959632 10531 Epo erythropoietin gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20959632 10531 Epo erythropoietin gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10409505 10531 Epo erythropoietin gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:7553874 10531 Epo erythropoietin gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:7553874 10531 Epo erythropoietin gene MP:0003913 increased heart right ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:15878311 10531 Epo erythropoietin gene MP:0003913 increased heart right ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:16330260 10531 Epo erythropoietin gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:15878311 10531 Epo erythropoietin gene MP:0004032 abnormal interventricular groove morphology IAGP N RGD:5509061 20141003 MGI PMID:10409505 10531 Epo erythropoietin gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:10409505 10531 Epo erythropoietin gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:12239150 10531 Epo erythropoietin gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:12239150 10531 Epo erythropoietin gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:12239150 10531 Epo erythropoietin gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:15878311 10531 Epo erythropoietin gene MP:0005575 increased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:15878311 10531 Epo erythropoietin gene MP:0005575 increased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:16330260 10531 Epo erythropoietin gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15531367 10531 Epo erythropoietin gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20141003 MGI PMID:12239150 10531 Epo erythropoietin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20959632 10531 Epo erythropoietin gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10409505 10531 Epo erythropoietin gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7553874 10531 Epo erythropoietin gene MP:0031589 detached epicardium IAGP N RGD:5509061 20240229 MGI PMID:10409505 10532 Epor erythropoietin receptor gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11158582 10532 Epor erythropoietin receptor gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11406592 10532 Epor erythropoietin receptor gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:23361909 10532 Epor erythropoietin receptor gene MP:0000216 absent erythroid progenitor cell IAGP N RGD:5509061 20141003 MGI PMID:8799165 10532 Epor erythropoietin receptor gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:11406592 10532 Epor erythropoietin receptor gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:19941827 10532 Epor erythropoietin receptor gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:23361909 10532 Epor erythropoietin receptor gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:23795291 10532 Epor erythropoietin receptor gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:7553874 10532 Epor erythropoietin receptor gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:8566749 10532 Epor erythropoietin receptor gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:10409505 10532 Epor erythropoietin receptor gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10409505 10532 Epor erythropoietin receptor gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16534010 10532 Epor erythropoietin receptor gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10409505 10532 Epor erythropoietin receptor gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:10409505 10532 Epor erythropoietin receptor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:23795291 10532 Epor erythropoietin receptor gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8799165 10532 Epor erythropoietin receptor gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:7553874 10532 Epor erythropoietin receptor gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:8566749 10532 Epor erythropoietin receptor gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:8799165 10532 Epor erythropoietin receptor gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:23795291 10532 Epor erythropoietin receptor gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:7553874 10532 Epor erythropoietin receptor gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:8566749 10532 Epor erythropoietin receptor gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:8799165 10532 Epor erythropoietin receptor gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10409505 10532 Epor erythropoietin receptor gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23361909 10532 Epor erythropoietin receptor gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23576758 10532 Epor erythropoietin receptor gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7553874 10532 Epor erythropoietin receptor gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8566749 10532 Epor erythropoietin receptor gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8799165 10532 Epor erythropoietin receptor gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8799165 10532 Epor erythropoietin receptor gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10409505 10532 Epor erythropoietin receptor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23795291 10532 Epor erythropoietin receptor gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:7553874 10532 Epor erythropoietin receptor gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:8799165 10532 Epor erythropoietin receptor gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:10409505 10532 Epor erythropoietin receptor gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:10409505 10532 Epor erythropoietin receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11158582 10532 Epor erythropoietin receptor gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:11158582 10532 Epor erythropoietin receptor gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:23795291 10532 Epor erythropoietin receptor gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8566749 10532 Epor erythropoietin receptor gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11158582 10532 Epor erythropoietin receptor gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11406592 10532 Epor erythropoietin receptor gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20210617 MGI PMID:33753942 10532 Epor erythropoietin receptor gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:23361909 10532 Epor erythropoietin receptor gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:11158582 10532 Epor erythropoietin receptor gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:11158582 10532 Epor erythropoietin receptor gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:11158582 10532 Epor erythropoietin receptor gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23361909 10532 Epor erythropoietin receptor gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23576758 10532 Epor erythropoietin receptor gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23361909 10532 Epor erythropoietin receptor gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23576758 10532 Epor erythropoietin receptor gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8566749 10532 Epor erythropoietin receptor gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8799165 10532 Epor erythropoietin receptor gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10409505 10532 Epor erythropoietin receptor gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 10532 Epor erythropoietin receptor gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:7553874 10532 Epor erythropoietin receptor gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 10532 Epor erythropoietin receptor gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:16534010 10532 Epor erythropoietin receptor gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20141003 MGI PMID:16534010 10532 Epor erythropoietin receptor gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:12606578 10532 Epor erythropoietin receptor gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20200820 MGI PMID:32093902 10532 Epor erythropoietin receptor gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:7553874 10532 Epor erythropoietin receptor gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8799165 10532 Epor erythropoietin receptor gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16534010 10532 Epor erythropoietin receptor gene MP:0004032 abnormal interventricular groove morphology IAGP N RGD:5509061 20141003 MGI PMID:10409505 10532 Epor erythropoietin receptor gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:10409505 10532 Epor erythropoietin receptor gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8566749 10532 Epor erythropoietin receptor gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16436614 10532 Epor erythropoietin receptor gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11158582 10532 Epor erythropoietin receptor gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:23361909 10532 Epor erythropoietin receptor gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:16534010 10532 Epor erythropoietin receptor gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20180503 MGI PMID:28169986 10532 Epor erythropoietin receptor gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180503 MGI PMID:28169986 10532 Epor erythropoietin receptor gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:11158582 10532 Epor erythropoietin receptor gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15531367 10532 Epor erythropoietin receptor gene MP:0008105 increased amacrine cell number IAGP N RGD:5509061 20200820 MGI PMID:32093902 10532 Epor erythropoietin receptor gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20200820 MGI PMID:32093902 10532 Epor erythropoietin receptor gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20200820 MGI PMID:32093902 10532 Epor erythropoietin receptor gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20200820 MGI PMID:32093902 10532 Epor erythropoietin receptor gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20200820 MGI PMID:32093902 10532 Epor erythropoietin receptor gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20180503 MGI PMID:28169986 10532 Epor erythropoietin receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20210617 MGI PMID:33753942 10532 Epor erythropoietin receptor gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23795291 10532 Epor erythropoietin receptor gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16534010 10532 Epor erythropoietin receptor gene MP:0010755 abnormal heart right ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:16534010 10532 Epor erythropoietin receptor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8566749 10532 Epor erythropoietin receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15090451 10532 Epor erythropoietin receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8799165 10532 Epor erythropoietin receptor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10409505 10532 Epor erythropoietin receptor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7553874 10532 Epor erythropoietin receptor gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11158582 10532 Epor erythropoietin receptor gene MP:0011243 decreased fetal derived definitive erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23795291 10532 Epor erythropoietin receptor gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:23361909 10532 Epor erythropoietin receptor gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200820 MGI PMID:32093902 10532 Epor erythropoietin receptor gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200820 MGI PMID:32093902 10532 Epor erythropoietin receptor gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200820 MGI PMID:32093902 10532 Epor erythropoietin receptor gene MP:0031276 abnormal stress erythropoiesis IAGP N RGD:5509061 20210805 MGI PMID:18854306 10532 Epor erythropoietin receptor gene MP:0031589 detached epicardium IAGP N RGD:5509061 20240229 MGI PMID:10409505 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:12052879 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11809799 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11984589 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12072561 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:12072561 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:7477377 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000296 absent trabeculae carneae IAGP N RGD:5509061 20141003 MGI PMID:10704452 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000296 absent trabeculae carneae IAGP N RGD:5509061 20141003 MGI PMID:11809799 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000296 absent trabeculae carneae IAGP N RGD:5509061 20141003 MGI PMID:9637684 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:7477377 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:12526770 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:10704452 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:10716706 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:10704452 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15044753 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:23792428 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19954518 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:7477377 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11564761 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15496447 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:19369542 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:7477377 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000992 absent primary muscle spindle IAGP N RGD:5509061 20141003 MGI PMID:12052879 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000995 absent secondary muscle spindle IAGP N RGD:5509061 20141003 MGI PMID:12052879 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0000996 partial loss of secondary muscle spindle IAGP N RGD:5509061 20141003 MGI PMID:12052879 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10704452 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15496447 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9637684 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19954518 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:12526770 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12526770 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:12702645 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7477377 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20160414 MGI PMID:7477377 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7477377 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7477377 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15496447 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001080 defasiculated phrenic nerve IAGP N RGD:5509061 20141003 MGI PMID:15496447 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:7477377 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:9637684 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:7477377 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001084 abnormal petrosal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:7477377 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001102 small superior vagus ganglion IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:10704452 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12526770 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:12526770 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18381417 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12702645 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19369542 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12052879 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10704452 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12052879 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19369542 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:12052879 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:19369542 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:12052879 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15496447 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12072561 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:11809799 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20150924 MGI PMID:25269082 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12526770 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20150924 MGI PMID:12955145 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20150924 MGI PMID:25269082 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:15496447 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:12702645 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12702645 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10716706 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10704452 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12052879 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12072561 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12526770 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:11809799 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20150924 MGI PMID:12955145 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12526770 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15496447 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:15051890 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12702645 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10704452 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:11984589 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:12072561 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:19369542 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:9637684 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20150924 MGI PMID:25269082 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20150924 MGI PMID:25269082 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20150924 MGI PMID:25269082 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:12072561 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:10704452 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20150924 MGI PMID:12955145 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:10704452 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:10704452 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0003994 abnormal dorsal spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:10704452 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:12702645 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:19369542 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0004075 decreased Schwann cell precursor number IAGP N RGD:5509061 20141003 MGI PMID:9637684 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:11984589 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:12052879 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:9637684 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10704452 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:12052879 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11984589 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:15044753 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11984589 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12072561 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0008317 abnormal paravertebral ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11809799 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0008317 abnormal paravertebral ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15051890 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0008468 absent muscle spindles IAGP N RGD:5509061 20141003 MGI PMID:12702645 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0008486 decreased muscle spindle number IAGP N RGD:5509061 20141003 MGI PMID:19369542 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20231221 MGI PMID:12072561 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0009505 abnormal mammary gland lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:15051890 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11984589 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15051890 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18381417 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0010493 abnormal atrium myocardium morphology IAGP N RGD:5509061 20150924 MGI PMID:25269082 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20150924 MGI PMID:25269082 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12072561 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15496447 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10704452 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7477377 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9637684 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11564761 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11809799 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15051890 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9362461 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20150924 MGI PMID:16466971 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20150924 MGI PMID:25269082 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20141003 MGI PMID:15496447 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:12052879 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:11984589 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0014317 decreased heart left ventricle septal wall thickness IAGP N RGD:5509061 20231109 MGI PMID:11984589 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0030972 increased myoblast apoptosis IAGP N RGD:5509061 20211125 MGI PMID:12052879 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:11984589 10533 Erbb2 erb-b2 receptor tyrosine kinase 2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:12072561 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20200402 MGI 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10022922 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0000478 delayed intestine development IAGP N RGD:5509061 20141003 MGI PMID:10022922 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10022922 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:15082767 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:10022922 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10022922 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:10022922 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10022922 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15082767 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15082767 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:10022922 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20200402 MGI 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:10022922 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20200402 MGI 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20200402 MGI 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20200402 MGI 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0005653 phototoxicity IAGP N RGD:5509061 20141003 MGI PMID:10022922 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0005653 phototoxicity IAGP N RGD:5509061 20141003 MGI PMID:15082767 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15082767 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10534 Ercc5 excision repair cross-complementing rodent repair deficiency, complementation group 5 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 10536 Ces1c carboxylesterase 1C gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20240307 MGI PMID:3101673 10536 Ces1c carboxylesterase 1C gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20240307 MGI PMID:7236294 10536 Ces1c carboxylesterase 1C gene MP:0005534 decreased body temperature IEA N RGD:5509061 20111116 MGI 10536 Ces1c carboxylesterase 1C gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20240307 MGI PMID:10945631 10536 Ces1c carboxylesterase 1C gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20240307 MGI PMID:3101673 10536 Ces1c carboxylesterase 1C gene MP:0008873 increased physiological sensitivity to xenobiotic IEA N RGD:5509061 20111116 MGI 10536 Ces1c carboxylesterase 1C gene MP:0008874 decreased physiological sensitivity to xenobiotic IEA N RGD:5509061 20111116 MGI 10536 Ces1c carboxylesterase 1C gene MP:0013275 abnormal xenobiotic metabolism IAGP N RGD:5509061 20240307 MGI PMID:10945631 10550 Esd esterase D/formylglutathione hydrolase gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 10550 Esd esterase D/formylglutathione hydrolase gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230601 MGI 10550 Esd esterase D/formylglutathione hydrolase gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11070086 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20667977 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:17803905 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20053716 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20150319 MGI PMID:16234973 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:14753739 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:12603601 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:9647203 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11160157 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:17332369 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:14745006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17785410 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:10213494 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:10919287 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:12019156 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:19574448 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:20667977 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:21873215 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:22800760 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10213494 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:12351685 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:17785410 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10510352 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:9391155 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:11311804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:20974921 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20180830 MGI PMID:29122548 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10600740 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11784006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21873215 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22800760 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8248223 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20180830 MGI PMID:29122548 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001123 dilated uterus IAGP N RGD:5509061 20141003 MGI PMID:17046690 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:10600740 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:10919287 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:12351685 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:17046690 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:24371309 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:8248223 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:10342864 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19439729 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:21873215 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:22800760 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:10342864 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:10600740 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:10919287 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:12351685 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:17046690 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:19439729 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:21149719 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:21873215 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:22800760 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:24371309 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:8248223 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20180830 MGI PMID:29122548 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001139 abnormal vagina morphology IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001140 abnormal vagina epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11784006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:10670526 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:8723431 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18755802 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:18755802 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:8723431 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:14753739 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:14753739 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:10558910 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11070086 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11784006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17495854 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20667977 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22800760 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:11095962 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:11593044 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:22800760 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10805804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:24739975 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001356 increased aggression towards female mice IAGP N RGD:5509061 20141003 MGI PMID:11114183 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001356 increased aggression towards female mice IAGP N RGD:5509061 20141003 MGI PMID:9832446 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:24739975 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001376 abnormal mating receptivity IAGP N RGD:5509061 20141003 MGI PMID:8248223 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001376 abnormal mating receptivity IAGP N RGD:5509061 20141003 MGI PMID:9832446 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:9832446 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:9832446 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:9832446 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:9832446 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:9037078 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:21444817 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:16234973 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:17803905 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:20053716 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11095962 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:24371309 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:12297545 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:24371309 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:10600740 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:14583652 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:19439729 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:20667977 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:21149719 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:21444817 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:24371309 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11380688 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:17785410 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10213494 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001884 mammary gland alveolar hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10213494 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001885 mammary gland duct hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10213494 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:8248223 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:19439729 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:19188600 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001924 infertility IAGP N RGD:5509061 20180830 MGI PMID:29122548 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10600740 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11698654 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18755802 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22800760 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10600740 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12351685 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17046690 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17947360 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19439729 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19574448 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:22800760 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:24371309 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8248223 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:17947360 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:19439729 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:21149719 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19439729 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:22800760 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002016 ovary cyst IAGP N RGD:5509061 20220407 MGI PMID:21149719 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17332369 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17332369 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:14753739 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:20053716 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10875230 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:14745006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10875230 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:20577047 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141204 MGI 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:11311804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:12603601 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12603601 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:21444817 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:9037078 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:10670526 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:11311804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:19574448 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:21873215 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10600740 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:19439729 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10600740 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10670526 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18755802 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8248223 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:19285805 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:14745006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:11593044 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:10558910 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:19439729 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:21149719 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17495854 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17495854 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:18755802 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:20667977 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:21444817 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:10805804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002865 increased growth rate IAGP N RGD:5509061 20141003 MGI PMID:20667977 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:17495854 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16234973 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:14745006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:14753739 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:24371309 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:10558910 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:10805804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:14753739 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:16234973 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20180830 MGI PMID:29122548 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:12351685 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003357 impaired granulosa cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003357 impaired granulosa cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003572 abnormal uterus development IAGP N RGD:5509061 20141003 MGI PMID:20667977 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:18755802 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:11557741 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:12603601 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17495854 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18063692 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:19188600 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:21444817 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:21873215 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:9393999 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:8248223 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:10510352 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:21444817 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16234973 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:11114183 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:24739975 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003969 abnormal luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:17046690 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0003969 abnormal luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:19439729 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:11074057 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24371309 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:16234973 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004348 long femur IAGP N RGD:5509061 20141003 MGI PMID:14753739 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:15283680 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:10775144 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:10558910 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:10558910 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:10805804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:16234973 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004728 abnormal efferent ductules of testis morphology IAGP N RGD:5509061 20141003 MGI PMID:10670526 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:14745006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:12603601 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10342864 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10919287 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19574448 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22800760 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:24371309 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17332369 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004850 abnormal testis weight IAGP N RGD:5509061 20141003 MGI PMID:9393999 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18755802 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:8248223 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:20577047 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:11070086 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004894 uterus atrophy IAGP N RGD:5509061 20141003 MGI PMID:11160157 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:11311804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:17046690 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:18755802 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004902 abnormal uterus size IAGP N RGD:5509061 20141003 MGI PMID:20974921 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004903 abnormal uterus weight IAGP N RGD:5509061 20141003 MGI PMID:11557741 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:12351685 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:16234973 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:10558910 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:11557741 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:11784006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:16234973 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:17495854 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:12351685 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10670526 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9393999 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11380688 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:10510352 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17803905 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:20053716 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:21444817 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:15283680 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:10805804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:17803905 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10875230 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11380688 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:10919287 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005133 increased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:21873215 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11095962 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:17495854 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:11784006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:16234973 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:19439729 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:21444817 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:21873215 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:8584021 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:12351685 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:24371309 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11070086 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19366879 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11070086 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11095962 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:19366879 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:11160157 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11160157 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19188600 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:19285805 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19366879 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22800760 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:10805804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:9171231 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:9037078 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11095962 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:14753739 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0006416 abnormal rete testis morphology IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0006423 dilated rete testis IAGP N RGD:5509061 20141003 MGI PMID:11698654 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0006423 dilated rete testis IAGP N RGD:5509061 20141003 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0006423 dilated rete testis IAGP N RGD:5509061 20141003 MGI PMID:9393999 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11380688 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11380688 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:14745006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10875230 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9647203 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10875230 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9647203 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008332 decreased lactotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9171231 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008334 increased gonadotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008335 decreased gonadotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:19439729 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:14745006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20141003 MGI PMID:11014235 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:14745006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008737 abnormal spleen physiology IAGP N RGD:5509061 20141003 MGI PMID:14745006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:14745006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:10919287 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18317592 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11784006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17332369 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008983 small vagina IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008984 vagina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008984 vagina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008984 vagina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008994 early vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:21149719 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:21873215 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:21149719 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009081 thin uterus IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009082 uterus cyst IAGP N RGD:5509061 20141003 MGI PMID:12351685 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009082 uterus cyst IAGP N RGD:5509061 20141003 MGI PMID:21873215 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12351685 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009096 decreased endometrial gland number IAGP N RGD:5509061 20141003 MGI PMID:21873215 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009097 absent endometrial glands IAGP N RGD:5509061 20141003 MGI PMID:17046690 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:11070086 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009130 increased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:11070086 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009140 dilated efferent ductule of testis IAGP N RGD:5509061 20141003 MGI PMID:10670526 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009140 dilated efferent ductule of testis IAGP N RGD:5509061 20141003 MGI PMID:11698654 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009140 dilated efferent ductule of testis IAGP N RGD:5509061 20141003 MGI PMID:9393999 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009205 abnormal internal male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:8723431 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009251 enlarged endometrial glands IAGP N RGD:5509061 20141003 MGI PMID:12351685 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009257 dilated seminiferous tubule IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009257 dilated seminiferous tubule IAGP N RGD:5509061 20141003 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21444817 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11095962 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11070086 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11070086 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009296 increased mammary fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009300 increased parametrial fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11070086 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11070086 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11095962 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009359 endometrium atrophy IAGP N RGD:5509061 20141003 MGI PMID:17046690 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12351685 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20220407 MGI PMID:24371309 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009365 abnormal theca cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17046690 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009365 abnormal theca cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009370 decreased theca cell number IAGP N RGD:5509061 20220407 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009371 increased theca cell number IAGP N RGD:5509061 20141003 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009371 increased theca cell number IAGP N RGD:5509061 20141003 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20141003 MGI PMID:10342864 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20141003 MGI PMID:10919287 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20141003 MGI PMID:11784006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20141003 MGI PMID:21149719 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20141003 MGI PMID:24371309 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20141003 MGI PMID:8248223 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20220407 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20220407 MGI PMID:17947360 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20220407 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:17785410 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009662 abnormal uterine receptivity IAGP N RGD:5509061 20141003 MGI PMID:20974921 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20141003 MGI PMID:12351685 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:11070086 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009697 abnormal copulation behavior IAGP N RGD:5509061 20240718 MGI PMID:11114183 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009736 abnormal prostate gland branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:18755802 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:14753739 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009824 spermatic granuloma IAGP N RGD:5509061 20141003 MGI PMID:10670526 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:10213494 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:12019156 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009856 failure of ejaculation IAGP N RGD:5509061 20141003 MGI PMID:11114183 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0009856 failure of ejaculation IAGP N RGD:5509061 20141003 MGI PMID:9037078 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11095962 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20667977 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:10805804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17332369 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12019156 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0010962 decreased compact bone mass IAGP N RGD:5509061 20141003 MGI PMID:20053716 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0010967 increased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:15283680 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:10805804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20150319 MGI PMID:16234973 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17332369 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:21873215 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:24371309 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0011128 increased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0011128 increased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:17046690 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0011128 increased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18339713 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17495854 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:17495854 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0011833 abnormal cremaster muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8723431 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0013613 abnormal volumetric bone mineral density IAGP N RGD:5509061 20150319 MGI PMID:16234973 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0013615 increased volumetric bone mineral density IAGP N RGD:5509061 20150319 MGI PMID:16234973 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0013616 decreased volumetric bone mineral density IAGP N RGD:5509061 20150319 MGI PMID:16234973 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0013618 decreased areal bone mineral density IAGP N RGD:5509061 20150319 MGI PMID:16234973 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0013618 decreased areal bone mineral density IAGP N RGD:5509061 20220915 MGI PMID:10805804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:17332369 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20190207 MGI PMID:28314781 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:10805804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:17803905 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160616 MGI PMID:17803905 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:15283680 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:17803905 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:15283680 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:14745006 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0021182 decreased femoral compact bone area IAGP N RGD:5509061 20220922 MGI PMID:10805804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0030985 decreased circulating osteocalcin level IAGP N RGD:5509061 20201001 MGI PMID:10805804 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10976058 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18953638 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:19423761 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220630 MGI PMID:10342864 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0031436 decreased copulatory plug deposition IAGP N RGD:5509061 20240718 MGI PMID:8895349 10551 Esr1 estrogen receptor 1 (alpha) gene MP:0031628 abnormal intromission IAGP N RGD:5509061 20240718 MGI PMID:9037078 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:14753739 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:12603601 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20733032 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15375213 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15375213 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:15781739 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000392 accelerated hair follicle regression IAGP N RGD:5509061 20141003 MGI PMID:15591132 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16477031 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:17522255 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17522255 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9861029 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11380688 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:11226319 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000836 abnormal substantia nigra morphology IAGP N RGD:5509061 20141003 MGI PMID:11226319 10552 Esr2 estrogen receptor 2 (beta) gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11226319 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10600740 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:10600740 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:9861029 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20170504 MGI PMID:25848008 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:10600740 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20170504 MGI PMID:25848008 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9861029 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:15591132 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:14753739 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12855748 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15781739 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:11095962 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10805804 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12855748 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:11114183 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001356 increased aggression towards female mice IAGP N RGD:5509061 20141003 MGI PMID:11114183 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:11593044 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15642619 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11593044 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:15642619 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11891272 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16054246 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11095962 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15375213 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:10600740 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:14583652 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11380688 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001884 mammary gland alveolar hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12438700 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9861029 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141204 MGI PMID:23580569 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10600740 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18268329 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10600740 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18268329 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001926 female infertility IAGP N RGD:5509061 20170504 MGI PMID:25848008 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:18268329 10552 Esr2 estrogen receptor 2 (beta) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9861029 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17332369 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12855748 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11226319 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002208 abnormal germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15044378 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:14612399 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:12603601 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12603601 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:11114183 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10600740 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:18268329 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:9861029 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10600740 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:19285805 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:11593044 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12855748 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:11593044 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:16477031 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002816 colitis IAGP N RGD:5509061 20150618 MGI PMID:17332369 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:15781739 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11799247 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19366879 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:15283680 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:20733032 10552 Esr2 estrogen receptor 2 (beta) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:16054246 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:11799247 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:14753739 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19366879 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:10805804 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:11226319 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:11226319 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20220630 MGI PMID:23580569 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003357 impaired granulosa cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:10927637 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:11380688 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:11557741 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:12603601 10552 Esr2 estrogen receptor 2 (beta) gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:11114183 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11799247 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004149 increased bone strength IAGP N RGD:5509061 20141003 MGI PMID:17535856 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004348 long femur IAGP N RGD:5509061 20141003 MGI PMID:14753739 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:17535856 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:15698835 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:15375213 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:10805804 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:11380688 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18317592 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004746 abnormal cochlear IHC afferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12062753 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20141003 MGI PMID:14612399 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:12603601 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:16477031 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:11593044 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12855748 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004903 abnormal uterus weight IAGP N RGD:5509061 20141003 MGI PMID:11557741 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:11557741 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:19366879 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11380688 10552 Esr2 estrogen receptor 2 (beta) gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:15283680 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11380688 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:12855748 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11095962 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:15781739 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11095962 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:19285805 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19366879 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19366879 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:10927637 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:11799247 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11799247 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15280152 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:15642619 10552 Esr2 estrogen receptor 2 (beta) gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11095962 10552 Esr2 estrogen receptor 2 (beta) gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12855748 10552 Esr2 estrogen receptor 2 (beta) gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:15375213 10552 Esr2 estrogen receptor 2 (beta) gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:12438700 10552 Esr2 estrogen receptor 2 (beta) gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:12438700 10552 Esr2 estrogen receptor 2 (beta) gene MP:0006416 abnormal rete testis morphology IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12855748 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:15375213 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11380688 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11380688 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17535856 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008532 decreased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:17980496 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11226319 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20141003 MGI PMID:15591132 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008869 anovulation IAGP N RGD:5509061 20170504 MGI PMID:25848008 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15698835 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16477031 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16477031 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17332369 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:11226319 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008983 small vagina IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0008984 vagina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009081 thin uterus IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19366879 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009257 dilated seminiferous tubule IAGP N RGD:5509061 20141003 MGI PMID:12855748 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11095962 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11095962 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20170504 MGI PMID:25848008 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009370 decreased theca cell number IAGP N RGD:5509061 20220407 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009372 abnormal cumulus oophorus morphology IAGP N RGD:5509061 20141003 MGI PMID:9861029 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20220407 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16054246 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16054246 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12438700 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15591132 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009646 urinary bladder inflammation IAGP N RGD:5509061 20141003 MGI PMID:17522255 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009648 abnormal superovulation IAGP N RGD:5509061 20220804 MGI PMID:9861029 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009697 abnormal copulation behavior IAGP N RGD:5509061 20240718 MGI PMID:11114183 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15781739 10552 Esr2 estrogen receptor 2 (beta) gene MP:0009856 failure of ejaculation IAGP N RGD:5509061 20141003 MGI PMID:11114183 10552 Esr2 estrogen receptor 2 (beta) gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11095962 10552 Esr2 estrogen receptor 2 (beta) gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17535856 10552 Esr2 estrogen receptor 2 (beta) gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:15642619 10552 Esr2 estrogen receptor 2 (beta) gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:10805804 10552 Esr2 estrogen receptor 2 (beta) gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17332369 10552 Esr2 estrogen receptor 2 (beta) gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:17522255 10552 Esr2 estrogen receptor 2 (beta) gene MP:0010967 increased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:15283680 10552 Esr2 estrogen receptor 2 (beta) gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:10805804 10552 Esr2 estrogen receptor 2 (beta) gene MP:0011128 increased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0011473 increased urine glycosaminoglycan level IAGP N RGD:5509061 20141003 MGI PMID:17522255 10552 Esr2 estrogen receptor 2 (beta) gene MP:0011747 myelofibrosis IAGP N RGD:5509061 20141003 MGI PMID:12740446 10552 Esr2 estrogen receptor 2 (beta) gene MP:0013616 decreased volumetric bone mineral density IAGP N RGD:5509061 20150319 MGI PMID:17535856 10552 Esr2 estrogen receptor 2 (beta) gene MP:0013618 decreased areal bone mineral density IAGP N RGD:5509061 20220915 MGI PMID:10805804 10552 Esr2 estrogen receptor 2 (beta) gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:17332369 10552 Esr2 estrogen receptor 2 (beta) gene MP:0014234 decreased enterocyte apoptosis IAGP N RGD:5509061 20230323 MGI PMID:16477031 10552 Esr2 estrogen receptor 2 (beta) gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:10805804 10552 Esr2 estrogen receptor 2 (beta) gene MP:0021182 decreased femoral compact bone area IAGP N RGD:5509061 20220922 MGI PMID:10805804 10552 Esr2 estrogen receptor 2 (beta) gene MP:0030985 decreased circulating osteocalcin level IAGP N RGD:5509061 20201002 MGI PMID:10805804 10552 Esr2 estrogen receptor 2 (beta) gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10976058 10552 Esr2 estrogen receptor 2 (beta) gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18268329 10552 Esr2 estrogen receptor 2 (beta) gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:25848008 10552 Esr2 estrogen receptor 2 (beta) gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:9861029 10552 Esr2 estrogen receptor 2 (beta) gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:25848008 10552 Esr2 estrogen receptor 2 (beta) gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:9861029 10552 Esr2 estrogen receptor 2 (beta) gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220630 MGI PMID:23580569 10552 Esr2 estrogen receptor 2 (beta) gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220804 MGI PMID:18268329 10552 Esr2 estrogen receptor 2 (beta) gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220804 MGI PMID:9861029 10552 Esr2 estrogen receptor 2 (beta) gene MP:0031650 decreased mounting behavior IAGP N RGD:5509061 20240905 MGI PMID:11114183 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20231102 MGI PMID:35899771 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231102 MGI PMID:35899771 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0000370 head blaze IEA N RGD:5509061 20160128 MGI 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0000373 belly spot IAGP N RGD:5509061 20231102 MGI PMID:35899771 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:9806641 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15384043 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15496469 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15384043 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15496469 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19411629 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16818745 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:9806641 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19411629 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15384043 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0002369 abnormal thymus subcapsular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:9806641 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0002938 white spotting IEA N RGD:5509061 20160128 MGI 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19411629 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:19411629 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9806641 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15384043 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9806641 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:9806641 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16818745 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15384043 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9806641 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231102 MGI PMID:35899771 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:9806641 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16818745 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16818745 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16818745 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:9806641 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15384043 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0008203 absent B-1a cells IAGP N RGD:5509061 20141003 MGI PMID:15384043 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15384043 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15384043 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15384043 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0009322 increased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0010428 abnormal heart right ventricle outflow tract morphology IAGP N RGD:5509061 20231102 MGI PMID:35899771 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20231102 MGI PMID:35899771 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20231102 MGI PMID:35899771 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9806641 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15384043 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15496469 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9806641 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9806641 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411629 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411629 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411629 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17339335 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411629 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0012745 abnormal neural crest cell physiology IAGP N RGD:5509061 20231102 MGI PMID:35899771 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0012749 decreased cardiac neural crest cell number IAGP N RGD:5509061 20231102 MGI PMID:35899771 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20231102 MGI PMID:35899771 10554 Ets1 E26 avian leukemia oncogene 1, 5' domain gene MP:0020321 increased vascular endothelial cell apoptosis IAGP N RGD:5509061 20160616 MGI PMID:19411629 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:9573048 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0000399 increased curvature of guard hairs IAGP N RGD:5509061 20141003 MGI PMID:9573048 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0000401 increased curvature of awl hairs IAGP N RGD:5509061 20141003 MGI PMID:9573048 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0000403 increased curvature of zigzag hairs IAGP N RGD:5509061 20141003 MGI PMID:9573048 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0000406 increased curvature of auchene hairs IAGP N RGD:5509061 20141003 MGI PMID:9573048 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:19411629 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:9573048 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16007139 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:9573048 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17977525 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9573048 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:17977525 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:14612405 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19411629 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19411629 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9573048 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17977525 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19411629 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:10485465 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:14612405 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:19847259 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:19411629 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17977525 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9573048 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:9573048 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9573048 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19847259 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16007139 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19847259 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17977525 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411629 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411629 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17977525 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411629 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9573048 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14612405 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411629 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411629 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411629 10555 Ets2 E26 avian leukemia oncogene 2, 3' domain gene MP:0020321 increased vascular endothelial cell apoptosis IAGP N RGD:5509061 20160616 MGI PMID:19411629 10556 F2r coagulation factor II thrombin receptor gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20160804 MGI PMID:25460576 10556 F2r coagulation factor II thrombin receptor gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20160804 MGI PMID:25460576 10556 F2r coagulation factor II thrombin receptor gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9918574 10556 F2r coagulation factor II thrombin receptor gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:11533492 10556 F2r coagulation factor II thrombin receptor gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:17967980 10556 F2r coagulation factor II thrombin receptor gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20152175 10556 F2r coagulation factor II thrombin receptor gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:20152175 10556 F2r coagulation factor II thrombin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20160804 MGI PMID:25460576 10556 F2r coagulation factor II thrombin receptor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:20152175 10556 F2r coagulation factor II thrombin receptor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11533492 10556 F2r coagulation factor II thrombin receptor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8632823 10556 F2r coagulation factor II thrombin receptor gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:8632823 10556 F2r coagulation factor II thrombin receptor gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:11533492 10556 F2r coagulation factor II thrombin receptor gene MP:0001762 polyuria IAGP N RGD:5509061 20160804 MGI PMID:25460576 10556 F2r coagulation factor II thrombin receptor gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20152175 10556 F2r coagulation factor II thrombin receptor gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17623652 10556 F2r coagulation factor II thrombin receptor gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18757438 10556 F2r coagulation factor II thrombin receptor gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11533492 10556 F2r coagulation factor II thrombin receptor gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22952456 10556 F2r coagulation factor II thrombin receptor gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:8972001 10556 F2r coagulation factor II thrombin receptor gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:18305483 10556 F2r coagulation factor II thrombin receptor gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:20152175 10556 F2r coagulation factor II thrombin receptor gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:22952456 10556 F2r coagulation factor II thrombin receptor gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:20152175 10556 F2r coagulation factor II thrombin receptor gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:22952456 10556 F2r coagulation factor II thrombin receptor gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:11120874 10556 F2r coagulation factor II thrombin receptor gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14980205 10556 F2r coagulation factor II thrombin receptor gene MP:0003228 abnormal sinus venosus morphology IAGP N RGD:5509061 20141003 MGI PMID:11533492 10556 F2r coagulation factor II thrombin receptor gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11533492 10556 F2r coagulation factor II thrombin receptor gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17967980 10556 F2r coagulation factor II thrombin receptor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11533492 10556 F2r coagulation factor II thrombin receptor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8632823 10556 F2r coagulation factor II thrombin receptor gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:8632823 10556 F2r coagulation factor II thrombin receptor gene MP:0004181 abnormal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:10591683 10556 F2r coagulation factor II thrombin receptor gene MP:0004348 long femur IAGP N RGD:5509061 20160804 MGI PMID:25460576 10556 F2r coagulation factor II thrombin receptor gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:10591683 10556 F2r coagulation factor II thrombin receptor gene MP:0005085 abnormal gallbladder physiology IAGP N RGD:5509061 20141003 MGI PMID:17431214 10556 F2r coagulation factor II thrombin receptor gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:11533492 10556 F2r coagulation factor II thrombin receptor gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:11533492 10556 F2r coagulation factor II thrombin receptor gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20160804 MGI PMID:25460576 10556 F2r coagulation factor II thrombin receptor gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11850418 10556 F2r coagulation factor II thrombin receptor gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8632823 10556 F2r coagulation factor II thrombin receptor gene MP:0006315 abnormal urine protein level IAGP N RGD:5509061 20160804 MGI PMID:25460576 10556 F2r coagulation factor II thrombin receptor gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20160804 MGI PMID:25460576 10556 F2r coagulation factor II thrombin receptor gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18305483 10556 F2r coagulation factor II thrombin receptor gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:15545995 10556 F2r coagulation factor II thrombin receptor gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18305483 10556 F2r coagulation factor II thrombin receptor gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:18305483 10556 F2r coagulation factor II thrombin receptor gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16434493 10556 F2r coagulation factor II thrombin receptor gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:16434493 10556 F2r coagulation factor II thrombin receptor gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:16434493 10556 F2r coagulation factor II thrombin receptor gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:20152175 10556 F2r coagulation factor II thrombin receptor gene MP:0009349 increased urine pH IAGP N RGD:5509061 20160804 MGI PMID:25460576 10556 F2r coagulation factor II thrombin receptor gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:17363687 10556 F2r coagulation factor II thrombin receptor gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16434493 10556 F2r coagulation factor II thrombin receptor gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18305483 10556 F2r coagulation factor II thrombin receptor gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:15345469 10556 F2r coagulation factor II thrombin receptor gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18757438 10556 F2r coagulation factor II thrombin receptor gene MP:0010695 abnormal blood pressure regulation IAGP N RGD:5509061 20141003 MGI PMID:8972001 10556 F2r coagulation factor II thrombin receptor gene MP:0010697 abnormal systemic arterial blood pressure regulation IAGP N RGD:5509061 20141003 MGI PMID:8972001 10556 F2r coagulation factor II thrombin receptor gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20160804 MGI PMID:25460576 10556 F2r coagulation factor II thrombin receptor gene MP:0010874 abnormal bone volume IAGP N RGD:5509061 20160804 MGI PMID:25460576 10556 F2r coagulation factor II thrombin receptor gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20160804 MGI PMID:25460576 10556 F2r coagulation factor II thrombin receptor gene MP:0010964 increased compact bone volume IAGP N RGD:5509061 20160804 MGI PMID:25460576 10556 F2r coagulation factor II thrombin receptor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11533492 10556 F2r coagulation factor II thrombin receptor gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16434493 10556 F2r coagulation factor II thrombin receptor gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11533492 10556 F2r coagulation factor II thrombin receptor gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8632823 10556 F2r coagulation factor II thrombin receptor gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8972001 10556 F2r coagulation factor II thrombin receptor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20152175 10556 F2r coagulation factor II thrombin receptor gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20160804 MGI PMID:25460576 10556 F2r coagulation factor II thrombin receptor gene MP:0021030 decreased tumor necrosis factor (ligand) superfamily member 11 level IAGP N RGD:5509061 20211230 MGI PMID:25460576 10556 F2r coagulation factor II thrombin receptor gene MP:0021032 increased tumor necrosis factor receptor superfamily member 11b level IAGP N RGD:5509061 20211230 MGI PMID:25460576 10557 F5 coagulation factor V gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200917 MGI PMID:8900278 10557 F5 coagulation factor V gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:8900278 10557 F5 coagulation factor V gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11533492 10557 F5 coagulation factor V gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:8900278 10557 F5 coagulation factor V gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20141003 MGI PMID:8900278 10557 F5 coagulation factor V gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10829076 10557 F5 coagulation factor V gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11533492 10557 F5 coagulation factor V gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8900278 10557 F5 coagulation factor V gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18344422 10557 F5 coagulation factor V gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10829076 10557 F5 coagulation factor V gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:11110695 10557 F5 coagulation factor V gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11110695 10557 F5 coagulation factor V gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11110695 10557 F5 coagulation factor V gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:10829076 10557 F5 coagulation factor V gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:11110695 10557 F5 coagulation factor V gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:11110695 10557 F5 coagulation factor V gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:11533492 10557 F5 coagulation factor V gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:11533492 10557 F5 coagulation factor V gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:18344422 10557 F5 coagulation factor V gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18344422 10557 F5 coagulation factor V gene MP:0010769 abnormal survival IAGP N RGD:5509061 20180322 MGI PMID:28827327 10557 F5 coagulation factor V gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8900278 10557 F5 coagulation factor V gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10829076 10557 F5 coagulation factor V gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11533492 10557 F5 coagulation factor V gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20180322 MGI PMID:28827327 10557 F5 coagulation factor V gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8900278 10557 F5 coagulation factor V gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180322 MGI PMID:11110695 10557 F5 coagulation factor V gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180322 MGI PMID:28827327 10557 F5 coagulation factor V gene MP:0011514 skin hemorrhage IAGP N RGD:5509061 20200917 MGI PMID:8900278 10559 F9 coagulation factor IX gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19583826 10559 F9 coagulation factor IX gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9354664 10559 F9 coagulation factor IX gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9354664 10559 F9 coagulation factor IX gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9354664 10559 F9 coagulation factor IX gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9639513 10559 F9 coagulation factor IX gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9354664 10559 F9 coagulation factor IX gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:19583826 10559 F9 coagulation factor IX gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:9326649 10559 F9 coagulation factor IX gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:9354664 10559 F9 coagulation factor IX gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:9639513 10559 F9 coagulation factor IX gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20180913 MGI PMID:26964564 10559 F9 coagulation factor IX gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:9326649 10559 F9 coagulation factor IX gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:15178576 10559 F9 coagulation factor IX gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:19583826 10559 F9 coagulation factor IX gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:9326649 10559 F9 coagulation factor IX gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:9639513 10559 F9 coagulation factor IX gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19583826 10559 F9 coagulation factor IX gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9639513 10559 F9 coagulation factor IX gene MP:0012305 umbilical cord hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9639513 10559 F9 coagulation factor IX gene MP:0012359 increased partial thromboplastin time IAGP N RGD:5509061 20180913 MGI PMID:26964564 10559 F9 coagulation factor IX gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20180913 MGI PMID:26964564 10563 Fabp1 fatty acid binding protein 1, liver gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20211021 MGI 10563 Fabp1 fatty acid binding protein 1, liver gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20231207 MGI 10563 Fabp1 fatty acid binding protein 1, liver gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:14534295 10563 Fabp1 fatty acid binding protein 1, liver gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12670956 10563 Fabp1 fatty acid binding protein 1, liver gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14534295 10563 Fabp1 fatty acid binding protein 1, liver gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14534295 10563 Fabp1 fatty acid binding protein 1, liver gene MP:0002139 abnormal hepatobiliary system physiology IAGP N RGD:5509061 20141003 MGI PMID:12670956 10563 Fabp1 fatty acid binding protein 1, liver gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14534295 10563 Fabp1 fatty acid binding protein 1, liver gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 10563 Fabp1 fatty acid binding protein 1, liver gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20210128 MGI 10563 Fabp1 fatty acid binding protein 1, liver gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14534295 10563 Fabp1 fatty acid binding protein 1, liver gene MP:0012361 decreased large unstained cell number IEA N RGD:5509061 20201022 MGI 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180719 MGI PMID:11023988 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180719 MGI PMID:11023988 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20180719 MGI PMID:11023988 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20180719 MGI PMID:11023988 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20180719 MGI PMID:11023988 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20180719 MGI PMID:11023988 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180719 MGI PMID:11023988 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210826 MGI 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210826 MGI 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180719 MGI PMID:11023988 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180719 MGI PMID:11023988 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20180719 MGI PMID:11023988 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20180719 MGI PMID:11023988 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0009307 decreased uterine fat pad weight IAGP N RGD:5509061 20180719 MGI PMID:11023988 10564 Fabp2 fatty acid binding protein 2, intestinal gene MP:0010511 shortened PR interval IEA N RGD:5509061 20240523 MGI 10565 Fabp6 fatty acid binding protein 6 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23251388 10565 Fabp6 fatty acid binding protein 6 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23251388 10565 Fabp6 fatty acid binding protein 6 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:23251388 10565 Fabp6 fatty acid binding protein 6 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23251388 10565 Fabp6 fatty acid binding protein 6 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23251388 10565 Fabp6 fatty acid binding protein 6 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23251388 10566 Fancc Fanconi anemia, complementation group C gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0000239 absent common myeloid progenitor cells IAGP N RGD:5509061 20141003 MGI PMID:8704201 10566 Fancc Fanconi anemia, complementation group C gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8704201 10566 Fancc Fanconi anemia, complementation group C gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:8630504 10566 Fancc Fanconi anemia, complementation group C gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:8704201 10566 Fancc Fanconi anemia, complementation group C gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:8630504 10566 Fancc Fanconi anemia, complementation group C gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:8630504 10566 Fancc Fanconi anemia, complementation group C gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:8630504 10566 Fancc Fanconi anemia, complementation group C gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:8630504 10566 Fancc Fanconi anemia, complementation group C gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:9596654 10566 Fancc Fanconi anemia, complementation group C gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:8630504 10566 Fancc Fanconi anemia, complementation group C gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:8704201 10566 Fancc Fanconi anemia, complementation group C gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8630504 10566 Fancc Fanconi anemia, complementation group C gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8630504 10566 Fancc Fanconi anemia, complementation group C gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8630504 10566 Fancc Fanconi anemia, complementation group C gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8704201 10566 Fancc Fanconi anemia, complementation group C gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:8630504 10566 Fancc Fanconi anemia, complementation group C gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:8630504 10566 Fancc Fanconi anemia, complementation group C gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:8704201 10566 Fancc Fanconi anemia, complementation group C gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:8704201 10566 Fancc Fanconi anemia, complementation group C gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8704201 10566 Fancc Fanconi anemia, complementation group C gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:8704201 10566 Fancc Fanconi anemia, complementation group C gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:8630504 10566 Fancc Fanconi anemia, complementation group C gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:8704201 10566 Fancc Fanconi anemia, complementation group C gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:8704201 10566 Fancc Fanconi anemia, complementation group C gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:8704201 10566 Fancc Fanconi anemia, complementation group C gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:8704201 10566 Fancc Fanconi anemia, complementation group C gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0005158 ovary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8704201 10566 Fancc Fanconi anemia, complementation group C gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:8704201 10566 Fancc Fanconi anemia, complementation group C gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20022886 10566 Fancc Fanconi anemia, complementation group C gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0008404 increased cellular sensitivity to methylmethanesulfonate IAGP N RGD:5509061 20141003 MGI PMID:9596654 10566 Fancc Fanconi anemia, complementation group C gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11493445 10566 Fancc Fanconi anemia, complementation group C gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9596654 10566 Fancc Fanconi anemia, complementation group C gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:20022886 10566 Fancc Fanconi anemia, complementation group C gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:11493445 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:12165533 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12165533 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18949059 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8252632 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9062348 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18949059 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0002531 abnormal type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:8759751 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:8759751 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0003423 reduced thrombolysis IAGP N RGD:5509061 20141003 MGI PMID:9586641 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12165533 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18949059 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:9062348 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:8252632 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:8759751 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18949059 10570 Fcer1a Fc receptor, IgE, high affinity I, alpha polypeptide gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:12165533 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:15073337 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:15073337 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15073337 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:9529325 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15073337 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:14722612 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:19251634 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:14722612 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0001588 abnormal hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:21258336 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:8313472 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:9739057 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:10843660 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8313472 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:9529325 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:10843660 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20141003 MGI PMID:12571859 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9739057 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15878887 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12571859 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14722612 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8313472 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9529325 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18776906 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:11911824 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14722612 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9062348 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12571859 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:9062348 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:12571859 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:12571859 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:16246361 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:15073337 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:12571859 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:15073337 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15878887 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:15878887 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0004260 enlarged placenta IAGP N RGD:5509061 20141003 MGI PMID:15878887 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:12571859 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12576552 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:17446931 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0004828 decreased susceptibility to autoimmune hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:17317854 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0004867 decreased platelet calcium level IAGP N RGD:5509061 20141003 MGI PMID:12586747 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:12571859 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:15073337 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:20664169 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11021533 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:9396764 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12571859 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10843660 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17446931 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10843660 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:9529325 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:8313472 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:9062348 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:15073337 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0005614 decreased susceptibility to type III hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:12571859 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10843660 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14722612 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:12586747 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9396764 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23602766 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:15073337 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008352 absent gamma-delta intraepithelial T cell IAGP N RGD:5509061 20141003 MGI PMID:9529325 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:15073337 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:10843660 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:10843660 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:10843660 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:10843660 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008559 abnormal interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23602766 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23602766 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10843660 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15878887 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9396764 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008680 abnormal interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:23602766 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:10843660 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008691 decreased interleukin-23 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20191128 MGI PMID:27887882 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:18776906 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:23602766 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008817 hematoma IAGP N RGD:5509061 20141003 MGI PMID:21258336 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23602766 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0008876 decreased uterine NK cell number IAGP N RGD:5509061 20141003 MGI PMID:15878887 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:16246361 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:20554973 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9739057 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23602766 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0010138 arteritis IAGP N RGD:5509061 20141003 MGI PMID:12571859 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8313472 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9396764 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:12571859 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12571859 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12571859 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:12571859 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0012529 abnormal decidua basalis morphology IAGP N RGD:5509061 20141003 MGI PMID:15878887 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0012726 abnormal uterine spiral artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15878887 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0012727 abnormal uterine spiral artery remodeling IAGP N RGD:5509061 20141003 MGI PMID:15878887 10572 Fcer1g Fc receptor, IgE, high affinity I, gamma polypeptide gene MP:0030072 round face IAGP N RGD:5509061 20170921 MGI PMID:15073337 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:11911823 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:11911824 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11911823 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22474370 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11911824 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:11911823 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18949059 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11911824 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18949059 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0002454 abnormal macrophage antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:11911823 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:11911824 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:9892619 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11911823 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0002531 abnormal type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11911824 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:11911824 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0004828 decreased susceptibility to autoimmune hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:11911824 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18949059 10573 Fcgr1 Fc receptor, IgG, high affinity I gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9892619 10576 Fga fibrinogen alpha chain gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:8929539 10576 Fga fibrinogen alpha chain gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:11906694 10576 Fga fibrinogen alpha chain gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:8929539 10576 Fga fibrinogen alpha chain gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12579195 10576 Fga fibrinogen alpha chain gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:7649481 10576 Fga fibrinogen alpha chain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7649481 10576 Fga fibrinogen alpha chain gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:10930441 10576 Fga fibrinogen alpha chain gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:8929539 10576 Fga fibrinogen alpha chain gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:12579195 10576 Fga fibrinogen alpha chain gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:8929539 10576 Fga fibrinogen alpha chain gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:8929539 10576 Fga fibrinogen alpha chain gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:9275201 10576 Fga fibrinogen alpha chain gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7649481 10576 Fga fibrinogen alpha chain gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:7649481 10576 Fga fibrinogen alpha chain gene MP:0004898 uterine hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7649481 10576 Fga fibrinogen alpha chain gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:8929539 10576 Fga fibrinogen alpha chain gene MP:0005245 hemarthrosis IAGP N RGD:5509061 20141003 MGI PMID:7649481 10576 Fga fibrinogen alpha chain gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:7649481 10576 Fga fibrinogen alpha chain gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:7649481 10576 Fga fibrinogen alpha chain gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10930441 10576 Fga fibrinogen alpha chain gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12579195 10576 Fga fibrinogen alpha chain gene MP:0011514 skin hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7649481 10576 Fga fibrinogen alpha chain gene MP:0012330 decreased circulating fibrinogen level IAGP N RGD:5509061 20200625 MGI PMID:7649481 10576 Fga fibrinogen alpha chain gene MP:0020215 impaired blood coagulation IAGP N RGD:5509061 20200625 MGI PMID:7649481 10576 Fga fibrinogen alpha chain gene MP:0031137 vaginal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:7649481 10576 Fga fibrinogen alpha chain gene MP:0031152 subcutaneous hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:7649481 10576 Fga fibrinogen alpha chain gene MP:0031153 stomach hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:8929539 10577 Fgf1 fibroblast growth factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10688672 10577 Fgf1 fibroblast growth factor 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:10688672 10577 Fgf1 fibroblast growth factor 1 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:10688672 10577 Fgf1 fibroblast growth factor 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10688672 10578 Fgf10 fibroblast growth factor 10 gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16513252 10578 Fgf10 fibroblast growth factor 10 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:12761848 10578 Fgf10 fibroblast growth factor 10 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:12761848 10578 Fgf10 fibroblast growth factor 10 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:12761848 10578 Fgf10 fibroblast growth factor 10 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:9916808 10578 Fgf10 fibroblast growth factor 10 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20211021 MGI 10578 Fgf10 fibroblast growth factor 10 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0000486 abnormal pulmonary trunk morphology IAGP N RGD:5509061 20141003 MGI PMID:16687131 10578 Fgf10 fibroblast growth factor 10 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16956603 10578 Fgf10 fibroblast growth factor 10 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:16956603 10578 Fgf10 fibroblast growth factor 10 gene MP:0000537 abnormal urethra morphology IAGP N RGD:5509061 20141003 MGI PMID:15340846 10578 Fgf10 fibroblast growth factor 10 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:12810586 10578 Fgf10 fibroblast growth factor 10 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:15340846 10578 Fgf10 fibroblast growth factor 10 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:19407009 10578 Fgf10 fibroblast growth factor 10 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:20171206 10578 Fgf10 fibroblast growth factor 10 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:21559415 10578 Fgf10 fibroblast growth factor 10 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:22719891 10578 Fgf10 fibroblast growth factor 10 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:9784490 10578 Fgf10 fibroblast growth factor 10 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:9916808 10578 Fgf10 fibroblast growth factor 10 gene MP:0000551 absent forelimb IAGP N RGD:5509061 20141003 MGI PMID:15234214 10578 Fgf10 fibroblast growth factor 10 gene MP:0000551 absent forelimb IAGP N RGD:5509061 20141003 MGI PMID:9784490 10578 Fgf10 fibroblast growth factor 10 gene MP:0000551 absent forelimb IAGP N RGD:5509061 20141003 MGI PMID:9916808 10578 Fgf10 fibroblast growth factor 10 gene MP:0000551 absent forelimb IAGP N RGD:5509061 20150903 MGI PMID:25468972 10578 Fgf10 fibroblast growth factor 10 gene MP:0000553 absent radius IAGP N RGD:5509061 20141003 MGI PMID:9916808 10578 Fgf10 fibroblast growth factor 10 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:15234214 10578 Fgf10 fibroblast growth factor 10 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:9784490 10578 Fgf10 fibroblast growth factor 10 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:9916808 10578 Fgf10 fibroblast growth factor 10 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:22719891 10578 Fgf10 fibroblast growth factor 10 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:12810586 10578 Fgf10 fibroblast growth factor 10 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:20171206 10578 Fgf10 fibroblast growth factor 10 gene MP:0000614 absent salivary gland IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0000618 small salivary gland IAGP N RGD:5509061 20210128 MGI PMID:26321752 10578 Fgf10 fibroblast growth factor 10 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20210128 MGI PMID:26321752 10578 Fgf10 fibroblast growth factor 10 gene MP:0000624 xerostomia IAGP N RGD:5509061 20210128 MGI PMID:26321752 10578 Fgf10 fibroblast growth factor 10 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:16687131 10578 Fgf10 fibroblast growth factor 10 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:11782400 10578 Fgf10 fibroblast growth factor 10 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:15199404 10578 Fgf10 fibroblast growth factor 10 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12761848 10578 Fgf10 fibroblast growth factor 10 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12941620 10578 Fgf10 fibroblast growth factor 10 gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12941620 10578 Fgf10 fibroblast growth factor 10 gene MP:0001159 absent prostate gland IAGP N RGD:5509061 20141003 MGI PMID:12941620 10578 Fgf10 fibroblast growth factor 10 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:12388344 10578 Fgf10 fibroblast growth factor 10 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19618463 10578 Fgf10 fibroblast growth factor 10 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:9784490 10578 Fgf10 fibroblast growth factor 10 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19618463 10578 Fgf10 fibroblast growth factor 10 gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:12388344 10578 Fgf10 fibroblast growth factor 10 gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:15234214 10578 Fgf10 fibroblast growth factor 10 gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:19618463 10578 Fgf10 fibroblast growth factor 10 gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:21559415 10578 Fgf10 fibroblast growth factor 10 gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:9784490 10578 Fgf10 fibroblast growth factor 10 gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:9916808 10578 Fgf10 fibroblast growth factor 10 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19618463 10578 Fgf10 fibroblast growth factor 10 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14530295 10578 Fgf10 fibroblast growth factor 10 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:14530295 10578 Fgf10 fibroblast growth factor 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21742743 10578 Fgf10 fibroblast growth factor 10 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19407009 10578 Fgf10 fibroblast growth factor 10 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:9916808 10578 Fgf10 fibroblast growth factor 10 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:19407009 10578 Fgf10 fibroblast growth factor 10 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20230601 MGI 10578 Fgf10 fibroblast growth factor 10 gene MP:0001314 cornea opacity IEA N RGD:5509061 20230601 MGI 10578 Fgf10 fibroblast growth factor 10 gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20181220 MGI PMID:10964474 10578 Fgf10 fibroblast growth factor 10 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 10578 Fgf10 fibroblast growth factor 10 gene MP:0001426 polydipsia IAGP N RGD:5509061 20210128 MGI PMID:26321752 10578 Fgf10 fibroblast growth factor 10 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160421 MGI 10578 Fgf10 fibroblast growth factor 10 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20171206 10578 Fgf10 fibroblast growth factor 10 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16720875 10578 Fgf10 fibroblast growth factor 10 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:20171206 10578 Fgf10 fibroblast growth factor 10 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:20171206 10578 Fgf10 fibroblast growth factor 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20171206 10578 Fgf10 fibroblast growth factor 10 gene MP:0002295 abnormal pulmonary circulation IAGP N RGD:5509061 20141003 MGI PMID:16687131 10578 Fgf10 fibroblast growth factor 10 gene MP:0002297 abnormal forced expiratory flow rates IAGP N RGD:5509061 20141003 MGI PMID:21742743 10578 Fgf10 fibroblast growth factor 10 gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20210128 MGI PMID:26321752 10578 Fgf10 fibroblast growth factor 10 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0002729 abnormal inner ear canal morphology IAGP N RGD:5509061 20141003 MGI PMID:12761848 10578 Fgf10 fibroblast growth factor 10 gene MP:0002770 absent bulbourethral gland IAGP N RGD:5509061 20141003 MGI PMID:12941620 10578 Fgf10 fibroblast growth factor 10 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19407009 10578 Fgf10 fibroblast growth factor 10 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:12810586 10578 Fgf10 fibroblast growth factor 10 gene MP:0003124 hypospadia IAGP N RGD:5509061 20141003 MGI PMID:15843416 10578 Fgf10 fibroblast growth factor 10 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:12761848 10578 Fgf10 fibroblast growth factor 10 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:12761848 10578 Fgf10 fibroblast growth factor 10 gene MP:0003165 absent superior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:12761848 10578 Fgf10 fibroblast growth factor 10 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15800000 10578 Fgf10 fibroblast growth factor 10 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19407009 10578 Fgf10 fibroblast growth factor 10 gene MP:0003334 pancreas fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0003595 epididymal cyst IAGP N RGD:5509061 20141003 MGI PMID:12941620 10578 Fgf10 fibroblast growth factor 10 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:15800000 10578 Fgf10 fibroblast growth factor 10 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:19618463 10578 Fgf10 fibroblast growth factor 10 gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:12941620 10578 Fgf10 fibroblast growth factor 10 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:15199404 10578 Fgf10 fibroblast growth factor 10 gene MP:0003760 decreased palatal length IAGP N RGD:5509061 20141003 MGI PMID:15199404 10578 Fgf10 fibroblast growth factor 10 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:12941620 10578 Fgf10 fibroblast growth factor 10 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:12388344 10578 Fgf10 fibroblast growth factor 10 gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20141003 MGI PMID:14623822 10578 Fgf10 fibroblast growth factor 10 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 10578 Fgf10 fibroblast growth factor 10 gene MP:0004035 abnormal sublingual gland morphology IAGP N RGD:5509061 20210128 MGI PMID:26321752 10578 Fgf10 fibroblast growth factor 10 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:9784490 10578 Fgf10 fibroblast growth factor 10 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:12761848 10578 Fgf10 fibroblast growth factor 10 gene MP:0004309 absent otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:12810586 10578 Fgf10 fibroblast growth factor 10 gene MP:0004309 absent otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:20171206 10578 Fgf10 fibroblast growth factor 10 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:12810586 10578 Fgf10 fibroblast growth factor 10 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:14623822 10578 Fgf10 fibroblast growth factor 10 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:20171206 10578 Fgf10 fibroblast growth factor 10 gene MP:0004313 absent vestibulocochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:14623822 10578 Fgf10 fibroblast growth factor 10 gene MP:0004317 small vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:12761848 10578 Fgf10 fibroblast growth factor 10 gene MP:0004352 absent humerus IAGP N RGD:5509061 20141003 MGI PMID:9916808 10578 Fgf10 fibroblast growth factor 10 gene MP:0004360 absent ulna IAGP N RGD:5509061 20141003 MGI PMID:9916808 10578 Fgf10 fibroblast growth factor 10 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9784490 10578 Fgf10 fibroblast growth factor 10 gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:12761848 10578 Fgf10 fibroblast growth factor 10 gene MP:0004573 absent limb buds IAGP N RGD:5509061 20141003 MGI PMID:21559415 10578 Fgf10 fibroblast growth factor 10 gene MP:0004573 absent limb buds IAGP N RGD:5509061 20141003 MGI PMID:9784490 10578 Fgf10 fibroblast growth factor 10 gene MP:0004830 short incisors IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:16956603 10578 Fgf10 fibroblast growth factor 10 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 10578 Fgf10 fibroblast growth factor 10 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 10578 Fgf10 fibroblast growth factor 10 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:19407009 10578 Fgf10 fibroblast growth factor 10 gene MP:0005314 absent thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0005315 absent pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:15800000 10578 Fgf10 fibroblast growth factor 10 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:9916808 10578 Fgf10 fibroblast growth factor 10 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:9784490 10578 Fgf10 fibroblast growth factor 10 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:12810586 10578 Fgf10 fibroblast growth factor 10 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:16687131 10578 Fgf10 fibroblast growth factor 10 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19407009 10578 Fgf10 fibroblast growth factor 10 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12761848 10578 Fgf10 fibroblast growth factor 10 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20230601 MGI 10578 Fgf10 fibroblast growth factor 10 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:12388344 10578 Fgf10 fibroblast growth factor 10 gene MP:0006285 absent inner ear IAGP N RGD:5509061 20141003 MGI PMID:12810586 10578 Fgf10 fibroblast growth factor 10 gene MP:0006288 small otic capsule IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0006402 small molars IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0008320 absent adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0008786 abnormal hindgut morphology IAGP N RGD:5509061 20141003 MGI PMID:16956603 10578 Fgf10 fibroblast growth factor 10 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0008881 absent Harderian gland IAGP N RGD:5509061 20181220 MGI PMID:10964474 10578 Fgf10 fibroblast growth factor 10 gene MP:0008904 abnormal mammary fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:11782400 10578 Fgf10 fibroblast growth factor 10 gene MP:0009479 abnormal cecum development IAGP N RGD:5509061 20141003 MGI PMID:14697353 10578 Fgf10 fibroblast growth factor 10 gene MP:0009479 abnormal cecum development IAGP N RGD:5509061 20141003 MGI PMID:16308329 10578 Fgf10 fibroblast growth factor 10 gene MP:0009479 abnormal cecum development IAGP N RGD:5509061 20141003 MGI PMID:16956603 10578 Fgf10 fibroblast growth factor 10 gene MP:0009479 abnormal cecum development IAGP N RGD:5509061 20141003 MGI PMID:22719891 10578 Fgf10 fibroblast growth factor 10 gene MP:0009509 absent rectum IAGP N RGD:5509061 20141003 MGI PMID:15234214 10578 Fgf10 fibroblast growth factor 10 gene MP:0009510 cecal atresia IAGP N RGD:5509061 20141003 MGI PMID:15234214 10578 Fgf10 fibroblast growth factor 10 gene MP:0009510 cecal atresia IAGP N RGD:5509061 20141003 MGI PMID:22719891 10578 Fgf10 fibroblast growth factor 10 gene MP:0009520 decreased submandibular gland size IAGP N RGD:5509061 20141003 MGI PMID:15972105 10578 Fgf10 fibroblast growth factor 10 gene MP:0009520 decreased submandibular gland size IAGP N RGD:5509061 20210128 MGI PMID:26321752 10578 Fgf10 fibroblast growth factor 10 gene MP:0009522 submandibular gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15972105 10578 Fgf10 fibroblast growth factor 10 gene MP:0009524 absent submandibular gland IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0009524 absent submandibular gland IAGP N RGD:5509061 20141003 MGI PMID:15972105 10578 Fgf10 fibroblast growth factor 10 gene MP:0009525 abnormal submandibular duct morphology IAGP N RGD:5509061 20141003 MGI PMID:15972105 10578 Fgf10 fibroblast growth factor 10 gene MP:0009571 abnormal right lung accessory lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:19618463 10578 Fgf10 fibroblast growth factor 10 gene MP:0009572 abnormal right lung cranial lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:19618463 10578 Fgf10 fibroblast growth factor 10 gene MP:0009573 abnormal right lung middle lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:19618463 10578 Fgf10 fibroblast growth factor 10 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141003 MGI PMID:15199404 10578 Fgf10 fibroblast growth factor 10 gene MP:0009884 palatal shelf fusion with tongue or mandible IAGP N RGD:5509061 20141003 MGI PMID:15199404 10578 Fgf10 fibroblast growth factor 10 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15199404 10578 Fgf10 fibroblast growth factor 10 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 10578 Fgf10 fibroblast growth factor 10 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 10578 Fgf10 fibroblast growth factor 10 gene MP:0010116 abnormal primitive urogenital sinus morphology IAGP N RGD:5509061 20141003 MGI PMID:12941620 10578 Fgf10 fibroblast growth factor 10 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0010489 abnormal heart atrium auricular region morphology IAGP N RGD:5509061 20141003 MGI PMID:16687131 10578 Fgf10 fibroblast growth factor 10 gene MP:0010521 absent pulmonary artery IAGP N RGD:5509061 20141003 MGI PMID:16687131 10578 Fgf10 fibroblast growth factor 10 gene MP:0010646 absent pulmonary vein IAGP N RGD:5509061 20141003 MGI PMID:16687131 10578 Fgf10 fibroblast growth factor 10 gene MP:0010794 abnormal stomach submucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0010906 abnormal lung bud morphology IAGP N RGD:5509061 20141003 MGI PMID:22719891 10578 Fgf10 fibroblast growth factor 10 gene MP:0010907 absent lung buds IAGP N RGD:5509061 20141003 MGI PMID:22719891 10578 Fgf10 fibroblast growth factor 10 gene MP:0010907 absent lung buds IAGP N RGD:5509061 20141003 MGI PMID:9916808 10578 Fgf10 fibroblast growth factor 10 gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:19618463 10578 Fgf10 fibroblast growth factor 10 gene MP:0010976 small lung lobe IAGP N RGD:5509061 20141003 MGI PMID:19618463 10578 Fgf10 fibroblast growth factor 10 gene MP:0011025 abnormal branching involved in trachea morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:9784490 10578 Fgf10 fibroblast growth factor 10 gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:15800000 10578 Fgf10 fibroblast growth factor 10 gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19618463 10578 Fgf10 fibroblast growth factor 10 gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:9784490 10578 Fgf10 fibroblast growth factor 10 gene MP:0011030 impaired branching involved in preterminal bronchiole morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:9784490 10578 Fgf10 fibroblast growth factor 10 gene MP:0011064 abnormal vestibular hair cell kinocilium morphology IAGP N RGD:5509061 20141003 MGI PMID:12761848 10578 Fgf10 fibroblast growth factor 10 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19618463 10578 Fgf10 fibroblast growth factor 10 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9784490 10578 Fgf10 fibroblast growth factor 10 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9916808 10578 Fgf10 fibroblast growth factor 10 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19407009 10578 Fgf10 fibroblast growth factor 10 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14623822 10578 Fgf10 fibroblast growth factor 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10578 Fgf10 fibroblast growth factor 10 gene MP:0011195 increased hair follicle apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0011305 dilated kidney calyx IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0011332 abnormal kidney outer medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0011333 abnormal kidney inner medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0011457 abnormal metanephric ureteric bud development IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0011759 absent Rathke's pouch IAGP N RGD:5509061 20141003 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0011884 absent colon IAGP N RGD:5509061 20160304 MGI PMID:16956603 10578 Fgf10 fibroblast growth factor 10 gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0013264 tongue ankylosis IAGP N RGD:5509061 20141003 MGI PMID:15199404 10578 Fgf10 fibroblast growth factor 10 gene MP:0013268 second pharyngeal arch hypoplasia IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0013269 third pharyngeal arch hypoplasia IAGP N RGD:5509061 20150924 MGI PMID:20035084 10578 Fgf10 fibroblast growth factor 10 gene MP:0013338 abnormal neurohypophysis development IAGP N RGD:5509061 20141211 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0013352 abnormal Rathke's pouch apoptosis IAGP N RGD:5509061 20141218 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0013445 Harderian gland atrophy IAGP N RGD:5509061 20150205 MGI PMID:19407009 10578 Fgf10 fibroblast growth factor 10 gene MP:0013495 decreased trachea gland number IAGP N RGD:5509061 20150305 MGI PMID:15973734 10578 Fgf10 fibroblast growth factor 10 gene MP:0013531 abnormal periderm development IAGP N RGD:5509061 20150219 MGI PMID:16720875 10578 Fgf10 fibroblast growth factor 10 gene MP:0013541 abnormal submandibular gland development IAGP N RGD:5509061 20210128 MGI PMID:26321752 10578 Fgf10 fibroblast growth factor 10 gene MP:0013580 abnormal nasal gland morphology IAGP N RGD:5509061 20170119 MGI PMID:27590203 10578 Fgf10 fibroblast growth factor 10 gene MP:0013582 abnormal lateral nasal gland morphology IAGP N RGD:5509061 20170119 MGI PMID:27590203 10578 Fgf10 fibroblast growth factor 10 gene MP:0013721 abnormal mammary placode morphology IAGP N RGD:5509061 20150402 MGI PMID:11782400 10578 Fgf10 fibroblast growth factor 10 gene MP:0013721 abnormal mammary placode morphology IAGP N RGD:5509061 20150402 MGI PMID:16720875 10578 Fgf10 fibroblast growth factor 10 gene MP:0013766 absent palatal rugae IAGP N RGD:5509061 20150430 MGI PMID:15199404 10578 Fgf10 fibroblast growth factor 10 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:16956603 10578 Fgf10 fibroblast growth factor 10 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 10578 Fgf10 fibroblast growth factor 10 gene MP:0021206 abnormal limb muscle morphology IAGP N RGD:5509061 20221201 MGI PMID:12388344 10578 Fgf10 fibroblast growth factor 10 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:15199404 10578 Fgf10 fibroblast growth factor 10 gene MP:0030920 small hair follicle bulb IAGP N RGD:5509061 20181220 MGI PMID:11062007 10578 Fgf10 fibroblast growth factor 10 gene MP:0031300 perineal hypospadia IAGP N RGD:5509061 20211014 MGI PMID:15234214 10578 Fgf10 fibroblast growth factor 10 gene MP:0031343 colon atresia IAGP N RGD:5509061 20220217 MGI PMID:22719891 10579 Fgf9 fibroblast growth factor 9 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0000088 short mandible IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:11493531 10579 Fgf9 fibroblast growth factor 9 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15621532 10579 Fgf9 fibroblast growth factor 9 gene MP:0000274 enlarged heart IEA N RGD:5509061 20160811 MGI 10579 Fgf9 fibroblast growth factor 9 gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:16308329 10579 Fgf9 fibroblast growth factor 9 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:18653563 10579 Fgf9 fibroblast growth factor 9 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0000566 synostosis IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0000566 synostosis IAGP N RGD:5509061 20141003 MGI PMID:19219044 10579 Fgf9 fibroblast growth factor 9 gene MP:0000566 synostosis IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:11290325 10579 Fgf9 fibroblast growth factor 9 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11493531 10579 Fgf9 fibroblast growth factor 9 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16496342 10579 Fgf9 fibroblast growth factor 9 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:21858205 10579 Fgf9 fibroblast growth factor 9 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:21858205 10579 Fgf9 fibroblast growth factor 9 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 10579 Fgf9 fibroblast growth factor 9 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 10579 Fgf9 fibroblast growth factor 9 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11493531 10579 Fgf9 fibroblast growth factor 9 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:18653563 10579 Fgf9 fibroblast growth factor 9 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 10579 Fgf9 fibroblast growth factor 9 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11290325 10579 Fgf9 fibroblast growth factor 9 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11493531 10579 Fgf9 fibroblast growth factor 9 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16496342 10579 Fgf9 fibroblast growth factor 9 gene MP:0001956 hypopnea IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:21858205 10579 Fgf9 fibroblast growth factor 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16496342 10579 Fgf9 fibroblast growth factor 9 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:11290325 10579 Fgf9 fibroblast growth factor 9 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15621532 10579 Fgf9 fibroblast growth factor 9 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15621532 10579 Fgf9 fibroblast growth factor 9 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15621532 10579 Fgf9 fibroblast growth factor 9 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20160421 MGI 10579 Fgf9 fibroblast growth factor 9 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 10579 Fgf9 fibroblast growth factor 9 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:11290325 10579 Fgf9 fibroblast growth factor 9 gene MP:0002996 ovotestis IAGP N RGD:5509061 20141003 MGI PMID:11290325 10579 Fgf9 fibroblast growth factor 9 gene MP:0003051 curly tail IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:11493531 10579 Fgf9 fibroblast growth factor 9 gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0003189 fused joints IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0003200 calcified joint IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20160811 MGI 10579 Fgf9 fibroblast growth factor 9 gene MP:0003416 premature bone ossification IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15621532 10579 Fgf9 fibroblast growth factor 9 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:16496342 10579 Fgf9 fibroblast growth factor 9 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16496342 10579 Fgf9 fibroblast growth factor 9 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0003742 narrow head IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0003758 narrow palate IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20141003 MGI PMID:11290325 10579 Fgf9 fibroblast growth factor 9 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0004592 small mandible IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0004676 wide ribs IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18653563 10579 Fgf9 fibroblast growth factor 9 gene MP:0004932 epididymis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11290325 10579 Fgf9 fibroblast growth factor 9 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:11493531 10579 Fgf9 fibroblast growth factor 9 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:21858205 10579 Fgf9 fibroblast growth factor 9 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:11493531 10579 Fgf9 fibroblast growth factor 9 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:18818193 10579 Fgf9 fibroblast growth factor 9 gene MP:0006418 abnormal testis cord formation IAGP N RGD:5509061 20141003 MGI PMID:11290325 10579 Fgf9 fibroblast growth factor 9 gene MP:0006419 disorganized testis cords IAGP N RGD:5509061 20141003 MGI PMID:11290325 10579 Fgf9 fibroblast growth factor 9 gene MP:0006421 decreased number of peritubular myoid cells IAGP N RGD:5509061 20141003 MGI PMID:11290325 10579 Fgf9 fibroblast growth factor 9 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:11493531 10579 Fgf9 fibroblast growth factor 9 gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0008159 increased diameter of fibula IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0008160 increased diameter of humerus IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0008161 increased diameter of radius IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0008162 increased diameter of tibia IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0008163 increased diameter of ulna IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:15621532 10579 Fgf9 fibroblast growth factor 9 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:11493531 10579 Fgf9 fibroblast growth factor 9 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0009880 decreased mouth size IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0009891 abnormal palate bone morphology IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0009906 increased tongue size IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0010114 abnormal coccyx morphology IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:11493531 10579 Fgf9 fibroblast growth factor 9 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16496342 10579 Fgf9 fibroblast growth factor 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11493531 10579 Fgf9 fibroblast growth factor 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11290325 10579 Fgf9 fibroblast growth factor 9 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16496342 10579 Fgf9 fibroblast growth factor 9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10579 Fgf9 fibroblast growth factor 9 gene MP:0011142 abnormal lung-associated mesenchyme development IAGP N RGD:5509061 20141003 MGI PMID:16540513 10579 Fgf9 fibroblast growth factor 9 gene MP:0011146 abnormal mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:11493531 10579 Fgf9 fibroblast growth factor 9 gene MP:0011692 increased chondrocyte number IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18818193 10579 Fgf9 fibroblast growth factor 9 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20171214 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0013550 abnormal secondary palate morphology IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0013602 abnormal Leydig cell differentiation IAGP N RGD:5509061 20150319 MGI PMID:11290325 10579 Fgf9 fibroblast growth factor 9 gene MP:0014299 increased cochlea size IAGP N RGD:5509061 20241031 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0014430 decreased hyaluronic acid level IAGP N RGD:5509061 20240425 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0014562 increased tympanic ring size IAGP N RGD:5509061 20241031 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0030032 high forehead IAGP N RGD:5509061 20170810 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171116 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171116 MGI PMID:19219044 10579 Fgf9 fibroblast growth factor 9 gene MP:0030354 premature sagittal suture closure IAGP N RGD:5509061 20171116 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0030372 enlarged Meckel's cartilage IAGP N RGD:5509061 20171207 MGI PMID:12140681 10579 Fgf9 fibroblast growth factor 9 gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20180628 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0030837 abnormal knee joint morphology IAGP N RGD:5509061 20181025 MGI PMID:28169396 10579 Fgf9 fibroblast growth factor 9 gene MP:0031213 increased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:21858205 10579 Fgf9 fibroblast growth factor 9 gene MP:0031306 abnormal cartilage physiology IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221117 MGI PMID:33959039 10579 Fgf9 fibroblast growth factor 9 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:33959039 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:10934262 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10934262 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:10934262 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:17132737 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20161110 MGI PMID:25966306 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17132737 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20160915 MGI PMID:21538817 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:18832392 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18297725 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20150716 MGI PMID:25843682 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20150716 MGI PMID:25843682 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:14530295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:14530295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000380 small hair follicles IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20141003 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000435 shortened head IAGP N RGD:5509061 20170907 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000435 shortened head IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17132737 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20160915 MGI PMID:21538817 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:15234214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:18653563 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:15581874 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:16442091 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:21128305 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:15581874 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141127 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000537 abnormal urethra morphology IAGP N RGD:5509061 20141003 MGI PMID:15340846 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000537 abnormal urethra morphology IAGP N RGD:5509061 20141003 MGI PMID:15843416 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:15340846 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000549 absent limbs IAGP N RGD:5509061 20150219 MGI PMID:24956260 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000551 absent forelimb IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000551 absent forelimb IAGP N RGD:5509061 20141003 MGI PMID:15234214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:15234214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000566 synostosis IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000629 absent mammary gland IAGP N RGD:5509061 20141003 MGI PMID:11782400 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000648 absent sebaceous gland IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000649 sebaceous gland atrophy IAGP N RGD:5509061 20141003 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000666 decreased prostate gland duct number IAGP N RGD:5509061 20141003 MGI PMID:12666202 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141127 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17418794 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:15199404 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000771 abnormal brain size IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:20077479 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20180301 MGI PMID:28483978 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19618463 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20150219 MGI PMID:24956260 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:15234214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20150716 MGI PMID:25843682 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:14530295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14530295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:14530295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20150716 MGI PMID:25843682 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:14530295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:16720875 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150716 MGI PMID:25843682 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17418794 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20180301 MGI PMID:28483978 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001341 absent eyelids IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001341 absent eyelids IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20141003 MGI PMID:18077586 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001426 polydipsia IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:18653563 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001669 abnormal intestinal glucose absorption IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17150206 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001677 absent apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:9560232 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19618463 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9435295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:9435295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:9435295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001725 abnormal umbilical cord morphology IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001874 acanthosis IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001874 acanthosis IAGP N RGD:5509061 20150716 MGI PMID:25843682 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20151112 MGI PMID:23358455 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20150716 MGI PMID:25843682 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20150716 MGI PMID:25843682 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:17132737 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002059 abnormal seminal vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12666202 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002059 abnormal seminal vesicle morphology IAGP N RGD:5509061 20150409 MGI PMID:3181757 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:9560232 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:16715082 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:20077479 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17132737 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17150206 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9435295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180705 MGI PMID:25264521 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16715082 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002295 abnormal pulmonary circulation IAGP N RGD:5509061 20141003 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:10934262 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14530295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:9560232 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18297725 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:17132737 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20150716 MGI PMID:25843682 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:15581874 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20150219 MGI PMID:24956260 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:15234214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:9560232 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003108 short zygomatic bone IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17132737 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003124 hypospadia IAGP N RGD:5509061 20141003 MGI PMID:15843416 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:17132737 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:9435295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10934262 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003315 abnormal perineum morphology IAGP N RGD:5509061 20141003 MGI PMID:15234214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:9435295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003418 premature intramembranous bone ossification IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10934262 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:14530295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20171207 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:15199404 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003760 decreased palatal length IAGP N RGD:5509061 20141003 MGI PMID:15199404 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003760 decreased palatal length IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141218 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003840 abnormal coronal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003840 abnormal coronal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003841 abnormal lambdoid suture morphology IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:9560232 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003853 dry skin IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:12559489 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141127 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9435295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004032 abnormal interventricular groove morphology IAGP N RGD:5509061 20141003 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004053 abnormal synchondrosis IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20150219 MGI PMID:24956260 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:12559489 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9435295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20180301 MGI PMID:28483978 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20180301 MGI PMID:28483978 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:10934262 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:9435295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004343 small scapula IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004346 absent acromion IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004380 short frontal bone IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20160915 MGI PMID:21538817 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004451 short presphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20160915 MGI PMID:21538817 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20160915 MGI PMID:21538817 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:15581874 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004507 abnormal ischium morphology IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004537 abnormal palatine bone horizontal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004552 fused tracheal cartilage rings IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:9435295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004573 absent limb buds IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004573 absent limb buds IAGP N RGD:5509061 20141003 MGI PMID:9435295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004606 absent vertebral spinous process IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004691 absent pubis IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:17418794 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004793 abnormal synaptic vesicle clustering IAGP N RGD:5509061 20141003 MGI PMID:17418794 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004831 long incisors IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18653563 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:15581874 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:16442091 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:21128305 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20150716 MGI PMID:25843682 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004961 increased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:12666202 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:9560232 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9435295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:20077479 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20160915 MGI PMID:21538817 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0005314 absent thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0005354 abnormal ilium morphology IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:10934262 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:15581874 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:16442091 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20150219 MGI PMID:24956260 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006213 shallow orbits IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006213 shallow orbits IAGP N RGD:5509061 20171019 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006213 shallow orbits IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006287 inner ear cyst IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006288 small otic capsule IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006288 small otic capsule IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0006400 decreased molar number IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008320 absent adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008320 absent adenohypophysis IAGP N RGD:5509061 20141127 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20170907 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008534 enlarged fourth ventricle IAGP N RGD:5509061 20141003 MGI PMID:20077479 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:20077479 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:20077479 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20150716 MGI PMID:25843682 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008785 abnormal sternum manubrium morphology IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:18832392 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009003 abnormal vibrissa number IAGP N RGD:5509061 20141003 MGI PMID:14530295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20150716 MGI PMID:25843682 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009051 dilated distal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:9435295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009479 abnormal cecum development IAGP N RGD:5509061 20141003 MGI PMID:14697353 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009509 absent rectum IAGP N RGD:5509061 20141003 MGI PMID:15234214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009510 cecal atresia IAGP N RGD:5509061 20141003 MGI PMID:15234214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009520 decreased submandibular gland size IAGP N RGD:5509061 20141003 MGI PMID:15972105 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009522 submandibular gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15972105 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009524 absent submandibular gland IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009524 absent submandibular gland IAGP N RGD:5509061 20141003 MGI PMID:15972105 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009524 absent submandibular gland IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009525 abnormal submandibular duct morphology IAGP N RGD:5509061 20141003 MGI PMID:15972105 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009545 abnormal dermis papillary layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009570 abnormal right lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20150716 MGI PMID:25843682 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009601 epidermis stratum granulosum hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009611 epidermis stratum spinosum hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141003 MGI PMID:15199404 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:9435295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009736 abnormal prostate gland branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12666202 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009884 palatal shelf fusion with tongue or mandible IAGP N RGD:5509061 20141003 MGI PMID:15199404 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:17132737 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15199404 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20231221 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010521 absent pulmonary artery IAGP N RGD:5509061 20141003 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010587 conotruncal ridge hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010646 absent pulmonary vein IAGP N RGD:5509061 20141003 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010647 heart left atrium hypoplasia IAGP N RGD:5509061 20231221 MGI PMID:16687131 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010678 abnormal skin adnexa morphology IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010911 abnormal pulmonary acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010979 small ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:16442091 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010979 small ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:21128305 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010980 ectopic ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:16442091 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010980 ectopic ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:21128305 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010982 abnormal ureteric bud elongation IAGP N RGD:5509061 20141003 MGI PMID:16442091 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:21128305 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:21128305 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010994 aerophagia IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0010998 pulmonary alveolar proteinosis IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011011 impaired lung lobe morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011011 impaired lung lobe morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011013 bronchiolectasis IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011026 impaired branching involved in trachea morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19618463 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17132737 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17418794 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17150206 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9560232 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12756187 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9435295 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011158 absent hypodermis muscle layer IAGP N RGD:5509061 20141003 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011185 absent primitive endoderm IAGP N RGD:5509061 20141003 MGI PMID:9560232 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16442091 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16442091 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21128305 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011387 absent metanephric mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:16442091 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16442091 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011485 abnormal urethra urothelium morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20141003 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20170907 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011627 decreased skin pigmentation IAGP N RGD:5509061 20171207 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011696 absent mast cells IAGP N RGD:5509061 20150716 MGI PMID:25843682 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011759 absent Rathke's pouch IAGP N RGD:5509061 20141218 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011772 genital tubercle hypoplasia IAGP N RGD:5509061 20151112 MGI PMID:23358455 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011861 increased cranium height IAGP N RGD:5509061 20141003 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011861 increased cranium height IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20170907 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20160915 MGI PMID:21538817 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20170921 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0012556 increased cell death IAGP N RGD:5509061 20180301 MGI PMID:28483978 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0012667 split sternal manubrium IAGP N RGD:5509061 20141003 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0012683 absent telencephalon IAGP N RGD:5509061 20180301 MGI PMID:28483978 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013192 decreased sebaceous gland number IAGP N RGD:5509061 20150716 MGI PMID:20308431 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013264 tongue ankylosis IAGP N RGD:5509061 20141003 MGI PMID:15199404 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013310 abnormal adrenal gland development IAGP N RGD:5509061 20141127 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013317 abnormal seminal vesicle development IAGP N RGD:5509061 20141204 MGI PMID:12666202 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013318 abnormal branching involved in seminal vesicle morphogenesis IAGP N RGD:5509061 20141204 MGI PMID:17202188 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013331 abnormal lacrimal gland development IAGP N RGD:5509061 20141204 MGI PMID:18077586 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013352 abnormal Rathke's pouch apoptosis IAGP N RGD:5509061 20141218 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013470 absent lacrimal gland bud IAGP N RGD:5509061 20150319 MGI PMID:18077586 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013578 abnormal stomach glandular region morphology IAGP N RGD:5509061 20150305 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013580 abnormal nasal gland morphology IAGP N RGD:5509061 20170119 MGI PMID:27590203 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013582 abnormal lateral nasal gland morphology IAGP N RGD:5509061 20170119 MGI PMID:27590203 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013721 abnormal mammary placode morphology IAGP N RGD:5509061 20150402 MGI PMID:16720875 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013766 absent palatal rugae IAGP N RGD:5509061 20150430 MGI PMID:15199404 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013785 abnormal mammary gland bud morphology IAGP N RGD:5509061 20150611 MGI PMID:11782400 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0013904 abnormal seminal vesicle muscle layer morphology IAGP N RGD:5509061 20150924 MGI PMID:12666202 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0014051 abnormal maxillary-premaxillary suture morphology IAGP N RGD:5509061 20171019 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0014152 absent exorbital lacrimal gland IAGP N RGD:5509061 20160407 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0020386 adipose tissue inflammation IAGP N RGD:5509061 20171207 MGI PMID:17304214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:15199404 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030064 small face IAGP N RGD:5509061 20170921 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030066 short face IAGP N RGD:5509061 20171207 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030066 short face IAGP N RGD:5509061 20171207 MGI PMID:17132737 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030076 abnormal cranial cavity morphology IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030167 decreased inner canthal distance IAGP N RGD:5509061 20171005 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030194 abnormal intermaxillary suture morphology IAGP N RGD:5509061 20171019 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030196 abnormal nasomaxillary suture morphology IAGP N RGD:5509061 20171012 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030200 abnormal nasal septum cartilage morphology IAGP N RGD:5509061 20171012 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030205 thick nasal septum IAGP N RGD:5509061 20171012 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030250 frontonasal prominence hypoplasia IAGP N RGD:5509061 20180301 MGI PMID:28483978 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030265 parietal bossing IAGP N RGD:5509061 20171109 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030275 thin frontal bone IAGP N RGD:5509061 20171102 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030281 thin parietal bone IAGP N RGD:5509061 20171102 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030301 abnormal maxillary frontal process morphology IAGP N RGD:5509061 20171102 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030301 abnormal maxillary frontal process morphology IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030302 abnormal maxillary zygomatic process morphology IAGP N RGD:5509061 20171102 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030302 abnormal maxillary zygomatic process morphology IAGP N RGD:5509061 20171102 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030315 small neurocranium IAGP N RGD:5509061 20171109 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171116 MGI PMID:14499350 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171116 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171116 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171207 MGI PMID:11274405 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171207 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171207 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171207 MGI PMID:17132737 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171207 MGI PMID:20077479 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171207 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171207 MGI PMID:21538817 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171207 MGI PMID:25966306 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171214 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030353 wide sagittal suture IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030356 premature lambdoid suture closure IAGP N RGD:5509061 20171214 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030358 premature squamoparietal suture closure IAGP N RGD:5509061 20171116 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030358 premature squamoparietal suture closure IAGP N RGD:5509061 20171207 MGI PMID:10631169 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030375 short zygomatic arch IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030390 premature facial suture closure IAGP N RGD:5509061 20171207 MGI PMID:21538817 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030391 premature zygomaticomaxillary suture closure IAGP N RGD:5509061 20171207 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030391 premature zygomaticomaxillary suture closure IAGP N RGD:5509061 20171207 MGI PMID:22585574 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030420 short basicranium IAGP N RGD:5509061 20171214 MGI PMID:15316116 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030420 short basicranium IAGP N RGD:5509061 20171214 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030420 short basicranium IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030424 premature palatomaxillary suture closure IAGP N RGD:5509061 20171214 MGI PMID:21538817 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030425 wide intermaxillary suture IAGP N RGD:5509061 20171214 MGI PMID:21538817 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030431 wide metopic suture IAGP N RGD:5509061 20171214 MGI PMID:15975938 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030431 wide metopic suture IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030434 premature maxillary-premaxillary suture closure IAGP N RGD:5509061 20171214 MGI PMID:21538817 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030436 premature frontonasal suture closure IAGP N RGD:5509061 20171214 MGI PMID:21538817 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030437 abnormal osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:12135917 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030438 increased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:20175913 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030443 abnormal cranial synchondrosis IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030445 abnormal sphenooccipital synchondrosis IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030446 premature sphenooccipital synchondrosis closure IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030448 premature presphenoid synchondrosis closure IAGP N RGD:5509061 20200521 MGI PMID:28123344 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030464 abnormal cranial cartilage morphology IAGP N RGD:5509061 20171228 MGI PMID:20503384 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030467 abnormal cranial cartilage development IAGP N RGD:5509061 20200514 MGI PMID:18242159 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:11180951 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0031300 perineal hypospadia IAGP N RGD:5509061 20211014 MGI PMID:15234214 10581 Fgfr2 fibroblast growth factor receptor 2 gene MP:0031525 thin left ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:16687131 10586 Fgg fibrinogen gamma chain gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16434491 10586 Fgg fibrinogen gamma chain gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:15304068 10586 Fgg fibrinogen gamma chain gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15304068 10586 Fgg fibrinogen gamma chain gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10980108 10586 Fgg fibrinogen gamma chain gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11891199 10586 Fgg fibrinogen gamma chain gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:11891199 10586 Fgg fibrinogen gamma chain gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:11891199 10586 Fgg fibrinogen gamma chain gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:11891199 10586 Fgg fibrinogen gamma chain gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:11891199 10586 Fgg fibrinogen gamma chain gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10980108 10586 Fgg fibrinogen gamma chain gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15304068 10586 Fgg fibrinogen gamma chain gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15173886 10586 Fgg fibrinogen gamma chain gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:15173886 10586 Fgg fibrinogen gamma chain gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:10980108 10586 Fgg fibrinogen gamma chain gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:15304068 10586 Fgg fibrinogen gamma chain gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:16434491 10586 Fgg fibrinogen gamma chain gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:15304068 10586 Fgg fibrinogen gamma chain gene MP:0003422 abnormal thrombolysis IAGP N RGD:5509061 20141003 MGI PMID:15304068 10586 Fgg fibrinogen gamma chain gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:11891199 10586 Fgg fibrinogen gamma chain gene MP:0004898 uterine hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11891199 10586 Fgg fibrinogen gamma chain gene MP:0004898 uterine hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15304068 10586 Fgg fibrinogen gamma chain gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:15304068 10586 Fgg fibrinogen gamma chain gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:16434491 10586 Fgg fibrinogen gamma chain gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:15304068 10586 Fgg fibrinogen gamma chain gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:8918453 10586 Fgg fibrinogen gamma chain gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:8918453 10586 Fgg fibrinogen gamma chain gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:8918453 10586 Fgg fibrinogen gamma chain gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15304068 10586 Fgg fibrinogen gamma chain gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17155952 10586 Fgg fibrinogen gamma chain gene MP:0012330 decreased circulating fibrinogen level IAGP N RGD:5509061 20200618 MGI PMID:15304068 10586 Fgg fibrinogen gamma chain gene MP:0031137 vaginal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:11891199 10586 Fgg fibrinogen gamma chain gene MP:0031434 increased miscarriage rate IAGP N RGD:5509061 20220915 MGI PMID:11891199 10587 Fh1 fumarate hydratase 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:17418408 10587 Fh1 fumarate hydratase 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:17418408 10587 Fh1 fumarate hydratase 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:23643539 10587 Fh1 fumarate hydratase 1 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:17418408 10587 Fh1 fumarate hydratase 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17418408 10587 Fh1 fumarate hydratase 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:23643539 10587 Fh1 fumarate hydratase 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17418408 10587 Fh1 fumarate hydratase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17418408 10587 Fh1 fumarate hydratase 1 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17418408 10587 Fh1 fumarate hydratase 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23643539 10587 Fh1 fumarate hydratase 1 gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20141003 MGI PMID:23643539 10587 Fh1 fumarate hydratase 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17418408 10587 Fh1 fumarate hydratase 1 gene MP:0011308 kidney corticomedullary cyst IAGP N RGD:5509061 20141003 MGI PMID:17418408 10587 Fh1 fumarate hydratase 1 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20230608 MGI PMID:23643539 10588 Fhl1 four and a half LIM domains 1 gene MP:0000751 myopathy IAGP N RGD:5509061 20160218 MGI PMID:25274776 10588 Fhl1 four and a half LIM domains 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160218 MGI PMID:25274776 10588 Fhl1 four and a half LIM domains 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:19033658 10588 Fhl1 four and a half LIM domains 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20141003 MGI 10588 Fhl1 four and a half LIM domains 1 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:19033658 10588 Fhl1 four and a half LIM domains 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 10588 Fhl1 four and a half LIM domains 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20160218 MGI PMID:25274776 10588 Fhl1 four and a half LIM domains 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20160218 MGI PMID:25274776 10588 Fhl1 four and a half LIM domains 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160218 MGI PMID:25274776 10588 Fhl1 four and a half LIM domains 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20160218 MGI PMID:25274776 10591 Foxg1 forkhead box G1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:19913004 10591 Foxg1 forkhead box G1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:24009395 10591 Foxg1 forkhead box G1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:12194867 10591 Foxg1 forkhead box G1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 10591 Foxg1 forkhead box G1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:16410827 10591 Foxg1 forkhead box G1 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:18404215 10591 Foxg1 forkhead box G1 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:19913004 10591 Foxg1 forkhead box G1 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 10591 Foxg1 forkhead box G1 gene MP:0000040 absent middle ear ossicles IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0000040 absent middle ear ossicles IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:12194867 10591 Foxg1 forkhead box G1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20141003 MGI PMID:21982646 10591 Foxg1 forkhead box G1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20230309 MGI PMID:23872235 10591 Foxg1 forkhead box G1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21982646 10591 Foxg1 forkhead box G1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:24043815 10591 Foxg1 forkhead box G1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230309 MGI PMID:23872235 10591 Foxg1 forkhead box G1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:17470284 10591 Foxg1 forkhead box G1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20141003 MGI PMID:12717732 10591 Foxg1 forkhead box G1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0000705 athymia IAGP N RGD:5509061 20150129 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:12441052 10591 Foxg1 forkhead box G1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17470284 10591 Foxg1 forkhead box G1 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17470284 10591 Foxg1 forkhead box G1 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18329011 10591 Foxg1 forkhead box G1 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20180301 MGI PMID:28483978 10591 Foxg1 forkhead box G1 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20230928 MGI PMID:37075751 10591 Foxg1 forkhead box G1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:12151532 10591 Foxg1 forkhead box G1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:17640820 10591 Foxg1 forkhead box G1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20230309 MGI PMID:23872235 10591 Foxg1 forkhead box G1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12773624 10591 Foxg1 forkhead box G1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17640820 10591 Foxg1 forkhead box G1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16917506 10591 Foxg1 forkhead box G1 gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20161117 MGI PMID:27001178 10591 Foxg1 forkhead box G1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:12773624 10591 Foxg1 forkhead box G1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:22378868 10591 Foxg1 forkhead box G1 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:15668733 10591 Foxg1 forkhead box G1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:19709628 10591 Foxg1 forkhead box G1 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17470284 10591 Foxg1 forkhead box G1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:21502507 10591 Foxg1 forkhead box G1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21502507 10591 Foxg1 forkhead box G1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20230309 MGI PMID:23872235 10591 Foxg1 forkhead box G1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:16436615 10591 Foxg1 forkhead box G1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:17050694 10591 Foxg1 forkhead box G1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:17470284 10591 Foxg1 forkhead box G1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:19709628 10591 Foxg1 forkhead box G1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0000935 abnormal folding of telencephalic vesicles IAGP N RGD:5509061 20141003 MGI PMID:17050694 10591 Foxg1 forkhead box G1 gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:17050694 10591 Foxg1 forkhead box G1 gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18155189 10591 Foxg1 forkhead box G1 gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:12773624 10591 Foxg1 forkhead box G1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18155189 10591 Foxg1 forkhead box G1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:12717732 10591 Foxg1 forkhead box G1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:17050694 10591 Foxg1 forkhead box G1 gene MP:0001296 macrophthalmia IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20180301 MGI PMID:28483978 10591 Foxg1 forkhead box G1 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:24009395 10591 Foxg1 forkhead box G1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:24009395 10591 Foxg1 forkhead box G1 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:18833191 10591 Foxg1 forkhead box G1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:15668733 10591 Foxg1 forkhead box G1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:12773624 10591 Foxg1 forkhead box G1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:24327562 10591 Foxg1 forkhead box G1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12773624 10591 Foxg1 forkhead box G1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:24043815 10591 Foxg1 forkhead box G1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18155189 10591 Foxg1 forkhead box G1 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:12441052 10591 Foxg1 forkhead box G1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17640820 10591 Foxg1 forkhead box G1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:19709628 10591 Foxg1 forkhead box G1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10837119 10591 Foxg1 forkhead box G1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:18404215 10591 Foxg1 forkhead box G1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 10591 Foxg1 forkhead box G1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16495313 10591 Foxg1 forkhead box G1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0002698 abnormal sclera morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:17470284 10591 Foxg1 forkhead box G1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:12773624 10591 Foxg1 forkhead box G1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:18487195 10591 Foxg1 forkhead box G1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22120178 10591 Foxg1 forkhead box G1 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 10591 Foxg1 forkhead box G1 gene MP:0003101 high myopia IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0003102 sclera thinning IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0003147 absent cochlea IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:16410827 10591 Foxg1 forkhead box G1 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:16495313 10591 Foxg1 forkhead box G1 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0003151 absent tunnel of Corti IAGP N RGD:5509061 20141003 MGI PMID:16410827 10591 Foxg1 forkhead box G1 gene MP:0003152 abnormal pillar cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17557302 10591 Foxg1 forkhead box G1 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0003166 decreased superior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0003169 abnormal scala media morphology IAGP N RGD:5509061 20141003 MGI PMID:18404215 10591 Foxg1 forkhead box G1 gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12574514 10591 Foxg1 forkhead box G1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12574514 10591 Foxg1 forkhead box G1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16917506 10591 Foxg1 forkhead box G1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17470284 10591 Foxg1 forkhead box G1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18155189 10591 Foxg1 forkhead box G1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16917506 10591 Foxg1 forkhead box G1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:18155189 10591 Foxg1 forkhead box G1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:17470284 10591 Foxg1 forkhead box G1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:17557302 10591 Foxg1 forkhead box G1 gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:15668733 10591 Foxg1 forkhead box G1 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:15668733 10591 Foxg1 forkhead box G1 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12194867 10591 Foxg1 forkhead box G1 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17557302 10591 Foxg1 forkhead box G1 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20230831 MGI PMID:34004180 10591 Foxg1 forkhead box G1 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18155189 10591 Foxg1 forkhead box G1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22378868 10591 Foxg1 forkhead box G1 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20230831 MGI PMID:34004180 10591 Foxg1 forkhead box G1 gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17557302 10591 Foxg1 forkhead box G1 gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0004236 absent masseter muscle IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0004238 absent pterygoid muscle IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 10591 Foxg1 forkhead box G1 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:24009395 10591 Foxg1 forkhead box G1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17050694 10591 Foxg1 forkhead box G1 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20180301 MGI PMID:28483978 10591 Foxg1 forkhead box G1 gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:18329011 10591 Foxg1 forkhead box G1 gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20180301 MGI PMID:28483978 10591 Foxg1 forkhead box G1 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:19709628 10591 Foxg1 forkhead box G1 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20180301 MGI PMID:28483978 10591 Foxg1 forkhead box G1 gene MP:0004282 retrognathia IAGP N RGD:5509061 20171214 MGI PMID:12717732 10591 Foxg1 forkhead box G1 gene MP:0004298 vestibular ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0004301 absent organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:12194867 10591 Foxg1 forkhead box G1 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0004311 otic vesicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0004312 absent pillar cells IAGP N RGD:5509061 20141003 MGI PMID:17557302 10591 Foxg1 forkhead box G1 gene MP:0004314 absent inner ear vestibule IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0004315 absent vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0004315 absent vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0004329 vestibular saccular degeneration IAGP N RGD:5509061 20141003 MGI PMID:24009395 10591 Foxg1 forkhead box G1 gene MP:0004330 abnormal vestibular saccular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:16495313 10591 Foxg1 forkhead box G1 gene MP:0004332 utricular degeneration IAGP N RGD:5509061 20141003 MGI PMID:24009395 10591 Foxg1 forkhead box G1 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 10591 Foxg1 forkhead box G1 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:16495313 10591 Foxg1 forkhead box G1 gene MP:0004336 small utricle IAGP N RGD:5509061 20141003 MGI PMID:16410827 10591 Foxg1 forkhead box G1 gene MP:0004369 absent utricle IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0004369 absent utricle IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:12194867 10591 Foxg1 forkhead box G1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16141228 10591 Foxg1 forkhead box G1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16495313 10591 Foxg1 forkhead box G1 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 10591 Foxg1 forkhead box G1 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16495313 10591 Foxg1 forkhead box G1 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20230831 MGI PMID:34004180 10591 Foxg1 forkhead box G1 gene MP:0004403 absent cochlear outer hair cells IAGP N RGD:5509061 20141003 MGI PMID:12194867 10591 Foxg1 forkhead box G1 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:16410827 10591 Foxg1 forkhead box G1 gene MP:0004406 abnormal cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16410827 10591 Foxg1 forkhead box G1 gene MP:0004408 decreased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:12194867 10591 Foxg1 forkhead box G1 gene MP:0004424 temporal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:12194867 10591 Foxg1 forkhead box G1 gene MP:0004497 decreased organ of Corti supporting cell number IAGP N RGD:5509061 20141003 MGI PMID:16141228 10591 Foxg1 forkhead box G1 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20180712 MGI PMID:27660326 10591 Foxg1 forkhead box G1 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20141003 MGI PMID:21982646 10591 Foxg1 forkhead box G1 gene MP:0004555 pharynx hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0004572 fusion of basioccipital and basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0004572 fusion of basioccipital and basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0004589 abnormal cochlear hair cell development IAGP N RGD:5509061 20141003 MGI PMID:12194867 10591 Foxg1 forkhead box G1 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:21982646 10591 Foxg1 forkhead box G1 gene MP:0004900 absent zygomatic arch IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0004922 abnormal common crus morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:12151532 10591 Foxg1 forkhead box G1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:17470284 10591 Foxg1 forkhead box G1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:22378868 10591 Foxg1 forkhead box G1 gene MP:0004979 abnormal neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:18155189 10591 Foxg1 forkhead box G1 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:21502507 10591 Foxg1 forkhead box G1 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:12441052 10591 Foxg1 forkhead box G1 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:17050694 10591 Foxg1 forkhead box G1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:17470284 10591 Foxg1 forkhead box G1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:18694563 10591 Foxg1 forkhead box G1 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:21982646 10591 Foxg1 forkhead box G1 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20230309 MGI PMID:23872235 10591 Foxg1 forkhead box G1 gene MP:0005195 abnormal posterior eye segment morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0005257 abnormal intraocular pressure IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:16917506 10591 Foxg1 forkhead box G1 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:18155189 10591 Foxg1 forkhead box G1 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20161201 MGI PMID:26670829 10591 Foxg1 forkhead box G1 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12151532 10591 Foxg1 forkhead box G1 gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17470284 10591 Foxg1 forkhead box G1 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20151001 MGI PMID:18404215 10591 Foxg1 forkhead box G1 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:18833191 10591 Foxg1 forkhead box G1 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:24009395 10591 Foxg1 forkhead box G1 gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:16917506 10591 Foxg1 forkhead box G1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:16917506 10591 Foxg1 forkhead box G1 gene MP:0006039 decreased mitochondrial fission IAGP N RGD:5509061 20141003 MGI PMID:16917506 10591 Foxg1 forkhead box G1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18155189 10591 Foxg1 forkhead box G1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21982646 10591 Foxg1 forkhead box G1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 10591 Foxg1 forkhead box G1 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:18404215 10591 Foxg1 forkhead box G1 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18404215 10591 Foxg1 forkhead box G1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20211014 MGI PMID:25417106 10591 Foxg1 forkhead box G1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20161117 MGI PMID:27001178 10591 Foxg1 forkhead box G1 gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0006241 abnormal placement of pupils IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16917506 10591 Foxg1 forkhead box G1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:17640820 10591 Foxg1 forkhead box G1 gene MP:0006285 absent inner ear IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0006286 inner ear hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0006289 otic capsule hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0006292 abnormal nasal placode morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0006292 abnormal nasal placode morphology IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0006331 abnormal patterning of the organ of Corti IAGP N RGD:5509061 20141003 MGI PMID:17557302 10591 Foxg1 forkhead box G1 gene MP:0008066 small endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:17470284 10591 Foxg1 forkhead box G1 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:18487195 10591 Foxg1 forkhead box G1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:18487195 10591 Foxg1 forkhead box G1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:12773624 10591 Foxg1 forkhead box G1 gene MP:0008285 abnormal hippocampus granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:12773624 10591 Foxg1 forkhead box G1 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17470284 10591 Foxg1 forkhead box G1 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20141003 MGI PMID:17470284 10591 Foxg1 forkhead box G1 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20180301 MGI PMID:28483978 10591 Foxg1 forkhead box G1 gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20141003 MGI PMID:18404215 10591 Foxg1 forkhead box G1 gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20141003 MGI PMID:19913004 10591 Foxg1 forkhead box G1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:17640820 10591 Foxg1 forkhead box G1 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12151532 10591 Foxg1 forkhead box G1 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18155189 10591 Foxg1 forkhead box G1 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:24043815 10591 Foxg1 forkhead box G1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:15668733 10591 Foxg1 forkhead box G1 gene MP:0009690 abnormal neural tube mantle layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12151532 10591 Foxg1 forkhead box G1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15668733 10591 Foxg1 forkhead box G1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0009899 hyoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:12151532 10591 Foxg1 forkhead box G1 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20161117 MGI PMID:27001178 10591 Foxg1 forkhead box G1 gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:15668733 10591 Foxg1 forkhead box G1 gene MP:0009974 decreased cerebral cortex pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:17640820 10591 Foxg1 forkhead box G1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20161117 MGI PMID:27001178 10591 Foxg1 forkhead box G1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15668733 10591 Foxg1 forkhead box G1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18833191 10591 Foxg1 forkhead box G1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20976199 10591 Foxg1 forkhead box G1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12194867 10591 Foxg1 forkhead box G1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12773624 10591 Foxg1 forkhead box G1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16452092 10591 Foxg1 forkhead box G1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17470284 10591 Foxg1 forkhead box G1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20736290 10591 Foxg1 forkhead box G1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21982646 10591 Foxg1 forkhead box G1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24327562 10591 Foxg1 forkhead box G1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7605629 10591 Foxg1 forkhead box G1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180712 MGI PMID:27660326 10591 Foxg1 forkhead box G1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10837119 10591 Foxg1 forkhead box G1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16410827 10591 Foxg1 forkhead box G1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17557302 10591 Foxg1 forkhead box G1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23971992 10591 Foxg1 forkhead box G1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20211014 MGI PMID:25417106 10591 Foxg1 forkhead box G1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12717732 10591 Foxg1 forkhead box G1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17050694 10591 Foxg1 forkhead box G1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12717732 10591 Foxg1 forkhead box G1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16917506 10591 Foxg1 forkhead box G1 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:17640820 10591 Foxg1 forkhead box G1 gene MP:0012556 increased cell death IAGP N RGD:5509061 20180301 MGI PMID:28483978 10591 Foxg1 forkhead box G1 gene MP:0012559 decreased forebrain volume IAGP N RGD:5509061 20141003 MGI PMID:17640820 10591 Foxg1 forkhead box G1 gene MP:0012683 absent telencephalon IAGP N RGD:5509061 20180301 MGI PMID:28483978 10591 Foxg1 forkhead box G1 gene MP:0013820 absent optic cup IAGP N RGD:5509061 20161201 MGI PMID:26670829 10591 Foxg1 forkhead box G1 gene MP:0014516 abnormal middle ear development IAGP N RGD:5509061 20240912 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0020083 decreased hippocampus volume IAGP N RGD:5509061 20170706 MGI PMID:17640820 10591 Foxg1 forkhead box G1 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:17640820 10591 Foxg1 forkhead box G1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20181011 MGI PMID:26107939 10591 Foxg1 forkhead box G1 gene MP:0030228 absent tubotympanic recess IAGP N RGD:5509061 20171019 MGI PMID:16600992 10591 Foxg1 forkhead box G1 gene MP:0030250 frontonasal prominence hypoplasia IAGP N RGD:5509061 20180301 MGI PMID:28483978 10591 Foxg1 forkhead box G1 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20171214 MGI PMID:12717732 10591 Foxg1 forkhead box G1 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20230309 MGI PMID:23872235 10591 Foxg1 forkhead box G1 gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:21982646 10592 Flg filaggrin gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:4557539 10592 Flg filaggrin gene MP:0000019 thick ears IAGP N RGD:5509061 20171102 MGI PMID:4557539 10592 Flg filaggrin gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20141003 MGI 10592 Flg filaggrin gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:23844115 10592 Flg filaggrin gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:23844115 10592 Flg filaggrin gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:23844115 10592 Flg filaggrin gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:4557539 10592 Flg filaggrin gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:23844115 10592 Flg filaggrin gene MP:0001230 epidermal desquamation IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:4557539 10592 Flg filaggrin gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:11121144 10592 Flg filaggrin gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:23844115 10592 Flg filaggrin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:4557539 10592 Flg filaggrin gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20181129 MGI PMID:25902485 10592 Flg filaggrin gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:11121144 10592 Flg filaggrin gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:19349982 10592 Flg filaggrin gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:23844115 10592 Flg filaggrin gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20181129 MGI PMID:25902485 10592 Flg filaggrin gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:23844115 10592 Flg filaggrin gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:4557539 10592 Flg filaggrin gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:19349982 10592 Flg filaggrin gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:19349982 10592 Flg filaggrin gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:19349982 10592 Flg filaggrin gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:22366455 10592 Flg filaggrin gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0003809 abnormal hair shaft morphology IEA N RGD:5509061 20141003 MGI 10592 Flg filaggrin gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0003846 matted coat IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0003848 brittle hair IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:19349982 10592 Flg filaggrin gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:23844115 10592 Flg filaggrin gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19349982 10592 Flg filaggrin gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:19349982 10592 Flg filaggrin gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19349982 10592 Flg filaggrin gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:19349982 10592 Flg filaggrin gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:19349982 10592 Flg filaggrin gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:19349982 10592 Flg filaggrin gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19349982 10592 Flg filaggrin gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:19349982 10592 Flg filaggrin gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:23844115 10592 Flg filaggrin gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19349982 10592 Flg filaggrin gene MP:0009598 thin epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:23844115 10592 Flg filaggrin gene MP:0009605 decreased keratohyalin granule number IAGP N RGD:5509061 20141003 MGI PMID:22409988 10592 Flg filaggrin gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20141003 MGI PMID:19349982 10592 Flg filaggrin gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0009795 epidermal spongiosis IAGP N RGD:5509061 20141003 MGI PMID:23844115 10592 Flg filaggrin gene MP:0009801 abnormal hair cortex keratinization IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:24084074 10592 Flg filaggrin gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:4557539 10592 Flg filaggrin gene MP:0010686 abnormal hair follicle matrix region morphology IEA N RGD:5509061 20141003 MGI 10592 Flg filaggrin gene MP:0012078 abnormal tail ring morphology IAGP N RGD:5509061 20170309 MGI PMID:4557539 10592 Flg filaggrin gene MP:0013178 tail necrosis IAGP N RGD:5509061 20170309 MGI PMID:4557539 10592 Flg filaggrin gene MP:0020084 short ears IAGP N RGD:5509061 20171102 MGI PMID:4557539 10593 Fmo1 flavin containing monooxygenase 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20240523 MGI PMID:34500002 10593 Fmo1 flavin containing monooxygenase 1 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20240523 MGI PMID:34500002 10593 Fmo1 flavin containing monooxygenase 1 gene MP:0014433 increased cytokine level IAGP N RGD:5509061 20240523 MGI PMID:34500002 10594 Fn1 fibronectin 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:8906418 10594 Fn1 fibronectin 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:17591922 10594 Fn1 fibronectin 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141127 MGI PMID:21320502 10594 Fn1 fibronectin 1 gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:12847088 10594 Fn1 fibronectin 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:12847088 10594 Fn1 fibronectin 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:17591922 10594 Fn1 fibronectin 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:11431694 10594 Fn1 fibronectin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17591922 10594 Fn1 fibronectin 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:8906418 10594 Fn1 fibronectin 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:8906418 10594 Fn1 fibronectin 1 gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:12847088 10594 Fn1 fibronectin 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15367684 10594 Fn1 fibronectin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12847088 10594 Fn1 fibronectin 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17591922 10594 Fn1 fibronectin 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11231631 10594 Fn1 fibronectin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14976060 10594 Fn1 fibronectin 1 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:8906418 10594 Fn1 fibronectin 1 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:11231631 10594 Fn1 fibronectin 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11231631 10594 Fn1 fibronectin 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17591922 10594 Fn1 fibronectin 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:17591922 10594 Fn1 fibronectin 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:8906418 10594 Fn1 fibronectin 1 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8906418 10594 Fn1 fibronectin 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0004573 absent limb buds IAGP N RGD:5509061 20141003 MGI PMID:17591922 10594 Fn1 fibronectin 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:8906418 10594 Fn1 fibronectin 1 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14976060 10594 Fn1 fibronectin 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141127 MGI PMID:21320502 10594 Fn1 fibronectin 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14976060 10594 Fn1 fibronectin 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:14976060 10594 Fn1 fibronectin 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:11231631 10594 Fn1 fibronectin 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:8906418 10594 Fn1 fibronectin 1 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20141003 MGI PMID:12847088 10594 Fn1 fibronectin 1 gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:17591922 10594 Fn1 fibronectin 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0010656 thick myocardium IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11431694 10594 Fn1 fibronectin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17591922 10594 Fn1 fibronectin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8906418 10594 Fn1 fibronectin 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17706958 10594 Fn1 fibronectin 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:12359774 10594 Fn1 fibronectin 1 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:17591922 10594 Fn1 fibronectin 1 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:8306876 10594 Fn1 fibronectin 1 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:8906418 10594 Fn1 fibronectin 1 gene MP:0012277 increased tail bud apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17591922 10594 Fn1 fibronectin 1 gene MP:0013200 head mesenchyme hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8906418 10594 Fn1 fibronectin 1 gene MP:0013258 abnormal extracellular matrix morphology IAGP N RGD:5509061 20141003 MGI PMID:12359774 10594 Fn1 fibronectin 1 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:12606706 10594 Fn1 fibronectin 1 gene MP:0031593 decreased cardiac jelly amount IAGP N RGD:5509061 20240229 MGI PMID:8306876 10595 Fnta farnesyltransferase, CAAX box, alpha gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201231 MGI 10595 Fnta farnesyltransferase, CAAX box, alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10595 Fnta farnesyltransferase, CAAX box, alpha gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 10595 Fnta farnesyltransferase, CAAX box, alpha gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 10597 Fosl1 fos-like antigen 1 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:15229648 10597 Fosl1 fos-like antigen 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:11044407 10597 Fosl1 fos-like antigen 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11044407 10597 Fosl1 fos-like antigen 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:11044407 10597 Fosl1 fos-like antigen 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:11044407 10597 Fosl1 fos-like antigen 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:11044407 10597 Fosl1 fos-like antigen 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15229648 10597 Fosl1 fos-like antigen 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11044407 10597 Fosl1 fos-like antigen 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:11044407 10597 Fosl1 fos-like antigen 1 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:15229648 10597 Fosl1 fos-like antigen 1 gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11044407 10597 Fosl1 fos-like antigen 1 gene MP:0004560 abnormal chorionic plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11044407 10597 Fosl1 fos-like antigen 1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:15229648 10597 Fosl1 fos-like antigen 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11044407 10597 Fosl1 fos-like antigen 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15229648 10597 Fosl1 fos-like antigen 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11044407 10597 Fosl1 fos-like antigen 1 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11044407 10597 Fosl1 fos-like antigen 1 gene MP:0011203 abnormal parietal yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:11044407 10597 Fosl1 fos-like antigen 1 gene MP:0020515 abnormal visceral yolk sac endoderm morphology IAGP N RGD:5509061 20180125 MGI PMID:11044407 10598 Fosl2 fos-like antigen 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18548006 10598 Fosl2 fos-like antigen 2 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141016 MGI PMID:24046454 10598 Fosl2 fos-like antigen 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17607691 10598 Fosl2 fos-like antigen 2 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:18548006 10598 Fosl2 fos-like antigen 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17607691 10598 Fosl2 fos-like antigen 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20171221 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:18548006 10598 Fosl2 fos-like antigen 2 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141016 MGI PMID:24046454 10598 Fosl2 fos-like antigen 2 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:18548006 10598 Fosl2 fos-like antigen 2 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141016 MGI PMID:24046454 10598 Fosl2 fos-like antigen 2 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:18548006 10598 Fosl2 fos-like antigen 2 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141016 MGI PMID:24046454 10598 Fosl2 fos-like antigen 2 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:18548006 10598 Fosl2 fos-like antigen 2 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141016 MGI PMID:24046454 10598 Fosl2 fos-like antigen 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141016 MGI PMID:24046454 10598 Fosl2 fos-like antigen 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141016 MGI PMID:24046454 10598 Fosl2 fos-like antigen 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:18548006 10598 Fosl2 fos-like antigen 2 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141016 MGI PMID:24046454 10598 Fosl2 fos-like antigen 2 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141016 MGI PMID:24046454 10598 Fosl2 fos-like antigen 2 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141016 MGI PMID:24046454 10598 Fosl2 fos-like antigen 2 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141016 MGI PMID:24046454 10598 Fosl2 fos-like antigen 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17607691 10598 Fosl2 fos-like antigen 2 gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:24046454 10598 Fosl2 fos-like antigen 2 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:15509771 10598 Fosl2 fos-like antigen 2 gene MP:0030985 decreased circulating osteocalcin level IAGP N RGD:5509061 20191219 MGI PMID:24046454 10599 Fpgs folylpolyglutamyl synthetase gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 10600 Fshb follicle stimulating hormone beta gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:9020850 10600 Fshb follicle stimulating hormone beta gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:9020850 10600 Fshb follicle stimulating hormone beta gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:9020850 10600 Fshb follicle stimulating hormone beta gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:9020850 10600 Fshb follicle stimulating hormone beta gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9020850 10600 Fshb follicle stimulating hormone beta gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:9020850 10600 Fshb follicle stimulating hormone beta gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11416011 10600 Fshb follicle stimulating hormone beta gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:9020850 10600 Fshb follicle stimulating hormone beta gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9020850 10600 Fshb follicle stimulating hormone beta gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:9020850 10600 Fshb follicle stimulating hormone beta gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:9020850 10600 Fshb follicle stimulating hormone beta gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:9020850 10600 Fshb follicle stimulating hormone beta gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:9020850 10600 Fshb follicle stimulating hormone beta gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11416011 10600 Fshb follicle stimulating hormone beta gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:9020850 10600 Fshb follicle stimulating hormone beta gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11416011 10600 Fshb follicle stimulating hormone beta gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:11416011 10600 Fshb follicle stimulating hormone beta gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:9020850 10600 Fshb follicle stimulating hormone beta gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:9020850 10600 Fshb follicle stimulating hormone beta gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:11416011 10600 Fshb follicle stimulating hormone beta gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:11416011 10600 Fshb follicle stimulating hormone beta gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20161027 MGI PMID:9020850 10601 Fshr follicle stimulating hormone receptor gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220929 MGI 10601 Fshr follicle stimulating hormone receptor gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0001140 abnormal vagina epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0001142 abnormal vagina orifice morphology IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:11466221 10601 Fshr follicle stimulating hormone receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 10601 Fshr follicle stimulating hormone receptor gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11466221 10601 Fshr follicle stimulating hormone receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11466221 10601 Fshr follicle stimulating hormone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11466221 10601 Fshr follicle stimulating hormone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:11466221 10601 Fshr follicle stimulating hormone receptor gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0002293 long gestation period IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0002661 abnormal corpus epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:15973687 10601 Fshr follicle stimulating hormone receptor gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15973687 10601 Fshr follicle stimulating hormone receptor gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0002678 increased follicle recruitment IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20141003 MGI PMID:11466221 10601 Fshr follicle stimulating hormone receptor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15973687 10601 Fshr follicle stimulating hormone receptor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:11466221 10601 Fshr follicle stimulating hormone receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0002782 abnormal testes secretion IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0003195 calcinosis IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0003529 enlarged clitoris IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:11466221 10601 Fshr follicle stimulating hormone receptor gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 10601 Fshr follicle stimulating hormone receptor gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20172968 10601 Fshr follicle stimulating hormone receptor gene MP:0004849 abnormal testis size IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11466221 10601 Fshr follicle stimulating hormone receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0004894 uterus atrophy IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0004894 uterus atrophy IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0004895 vagina atrophy IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0004898 uterine hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:11466221 10601 Fshr follicle stimulating hormone receptor gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15973687 10601 Fshr follicle stimulating hormone receptor gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0005102 abnormal iris pigmentation IEA N RGD:5509061 20240523 MGI 10601 Fshr follicle stimulating hormone receptor gene MP:0005131 increased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0005131 increased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0005133 increased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20141003 MGI PMID:11466221 10601 Fshr follicle stimulating hormone receptor gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15973687 10601 Fshr follicle stimulating hormone receptor gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0006361 abnormal female germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:11466221 10601 Fshr follicle stimulating hormone receptor gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0008334 increased gonadotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0008337 increased thyrotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0008975 delayed male fertility IAGP N RGD:5509061 20141003 MGI PMID:11466221 10601 Fshr follicle stimulating hormone receptor gene MP:0008976 delayed female fertility IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0008980 decreased vagina weight IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0008994 early vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:14502087 10601 Fshr follicle stimulating hormone receptor gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:11459817 10601 Fshr follicle stimulating hormone receptor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0009016 abnormal estrus IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0009081 thin uterus IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0009081 thin uterus IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0009082 uterus cyst IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0009090 myometrium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0009094 abnormal endometrial gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0009221 uterus adenomyosis IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0009222 increased uterus tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:15973687 10601 Fshr follicle stimulating hormone receptor gene MP:0009231 detached acrosome IAGP N RGD:5509061 20141003 MGI PMID:15973687 10601 Fshr follicle stimulating hormone receptor gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15973687 10601 Fshr follicle stimulating hormone receptor gene MP:0009233 enlarged sperm head IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0009248 small caput epididymis IAGP N RGD:5509061 20141003 MGI PMID:15973687 10601 Fshr follicle stimulating hormone receptor gene MP:0009251 enlarged endometrial glands IAGP N RGD:5509061 20141003 MGI PMID:12193578 10601 Fshr follicle stimulating hormone receptor gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20141003 MGI PMID:15973687 10601 Fshr follicle stimulating hormone receptor gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 10601 Fshr follicle stimulating hormone receptor gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 10601 Fshr follicle stimulating hormone receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:12135868 10601 Fshr follicle stimulating hormone receptor gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10775161 10601 Fshr follicle stimulating hormone receptor gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 10601 Fshr follicle stimulating hormone receptor gene MP:0013348 adenohypophysis hyperplasia IAGP N RGD:5509061 20150129 MGI PMID:9811848 10601 Fshr follicle stimulating hormone receptor gene MP:0014270 decreased ovary secretion IAGP N RGD:5509061 20230810 MGI PMID:10803590 10601 Fshr follicle stimulating hormone receptor gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:11089565 10601 Fshr follicle stimulating hormone receptor gene MP:0030826 decreased femur weight IAGP N RGD:5509061 20181018 MGI PMID:11089565 10603 Fst follistatin gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20240523 MGI 10603 Fst follistatin gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:14701941 10603 Fst follistatin gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:24019467 10603 Fst follistatin gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:14701941 10603 Fst follistatin gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20810712 10603 Fst follistatin gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 10603 Fst follistatin gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:14701941 10603 Fst follistatin gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:14701941 10603 Fst follistatin gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:14701941 10603 Fst follistatin gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:20032047 10603 Fst follistatin gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14701941 10603 Fst follistatin gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:14701941 10603 Fst follistatin gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:20032047 10603 Fst follistatin gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:14701941 10603 Fst follistatin gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:20810712 10603 Fst follistatin gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:14701941 10603 Fst follistatin gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 10603 Fst follistatin gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:14701941 10603 Fst follistatin gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:15976303 10603 Fst follistatin gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20141003 MGI PMID:20810712 10603 Fst follistatin gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20810712 10603 Fst follistatin gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:24019467 10603 Fst follistatin gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0003346 abnormal pectoral muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:20810712 10603 Fst follistatin gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 10603 Fst follistatin gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0004246 abnormal extensor digitorum longus morphology IAGP N RGD:5509061 20141003 MGI PMID:20810712 10603 Fst follistatin gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:24019467 10603 Fst follistatin gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0004648 decreased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:24019467 10603 Fst follistatin gene MP:0004650 increased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:24019467 10603 Fst follistatin gene MP:0004791 absent lower incisors IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14701941 10603 Fst follistatin gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:12546816 10603 Fst follistatin gene MP:0005359 growth retardation of incisors IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15976303 10603 Fst follistatin gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12546816 10603 Fst follistatin gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:15976303 10603 Fst follistatin gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12546816 10603 Fst follistatin gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20810712 10603 Fst follistatin gene MP:0008922 abnormal cervical rib IAGP N RGD:5509061 20141003 MGI PMID:24019467 10603 Fst follistatin gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:20032047 10603 Fst follistatin gene MP:0009361 abnormal primordial ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20032047 10603 Fst follistatin gene MP:0009422 decreased gastrocnemius weight IAGP N RGD:5509061 20141003 MGI PMID:20810712 10603 Fst follistatin gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0009894 absent hard palate IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:12546816 10603 Fst follistatin gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 10603 Fst follistatin gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:20810712 10603 Fst follistatin gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:20810712 10603 Fst follistatin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7885475 10603 Fst follistatin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 10603 Fst follistatin gene MP:0011124 increased primary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20032047 10603 Fst follistatin gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:14701941 10603 Fst follistatin gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20032047 10603 Fst follistatin gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20032047 10603 Fst follistatin gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20032047 10603 Fst follistatin gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:14701941 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:14757696 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:14751857 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14751857 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14751857 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20141003 MGI PMID:14751857 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:14751857 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0003891 increased allantois apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:14751857 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0005563 abnormal hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:14751857 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12777375 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0012606 increased glutathione level IAGP N RGD:5509061 20180111 MGI PMID:17693254 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:12169625 10608 G6pdx glucose-6-phosphate dehydrogenase X-linked gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:12169625 10610 Gabra3 gamma-aminobutyric acid type A receptor subunit alpha 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220428 MGI 10610 Gabra3 gamma-aminobutyric acid type A receptor subunit alpha 3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20111116 MGI 10610 Gabra3 gamma-aminobutyric acid type A receptor subunit alpha 3 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:16284244 10610 Gabra3 gamma-aminobutyric acid type A receptor subunit alpha 3 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:16284244 10610 Gabra3 gamma-aminobutyric acid type A receptor subunit alpha 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:16284244 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160204 MGI PMID:24281383 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20160204 MGI PMID:24281383 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0001987 alcohol preference IAGP N RGD:5509061 20160204 MGI PMID:24281383 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20160204 MGI PMID:24281383 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20160204 MGI PMID:24281383 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20160204 MGI PMID:24281383 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20160204 MGI PMID:24281383 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20160204 MGI PMID:24281383 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20160204 MGI PMID:24281383 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20160204 MGI PMID:24281383 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0005138 decreased prolactin level IAGP N RGD:5509061 20160204 MGI PMID:24281383 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20160204 MGI PMID:24281383 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20160204 MGI PMID:24281383 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:24281383 10611 Gabrb1 gamma-aminobutyric acid type A receptor subunit beta 1 gene MP:0014384 increased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:24281383 10612 Gabrb2 gamma-aminobutyric acid type A receptor subunit beta 2 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:17021187 10612 Gabrb2 gamma-aminobutyric acid type A receptor subunit beta 2 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20220421 MGI PMID:11331371 10612 Gabrb2 gamma-aminobutyric acid type A receptor subunit beta 2 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021187 10612 Gabrb2 gamma-aminobutyric acid type A receptor subunit beta 2 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:11331371 10612 Gabrb2 gamma-aminobutyric acid type A receptor subunit beta 2 gene MP:0004287 abnormal spiral limbus morphology IAGP N RGD:5509061 20141003 MGI PMID:17021187 10612 Gabrb2 gamma-aminobutyric acid type A receptor subunit beta 2 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021187 10612 Gabrb2 gamma-aminobutyric acid type A receptor subunit beta 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021187 10612 Gabrb2 gamma-aminobutyric acid type A receptor subunit beta 2 gene MP:0004490 type IV spiral ligament fibrocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021187 10612 Gabrb2 gamma-aminobutyric acid type A receptor subunit beta 2 gene MP:0004632 abnormal cochlear OHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17021187 10612 Gabrb2 gamma-aminobutyric acid type A receptor subunit beta 2 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:17021187 10612 Gabrb2 gamma-aminobutyric acid type A receptor subunit beta 2 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:17021187 10612 Gabrb2 gamma-aminobutyric acid type A receptor subunit beta 2 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:13679430 10612 Gabrb2 gamma-aminobutyric acid type A receptor subunit beta 2 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:17021187 10612 Gabrb2 gamma-aminobutyric acid type A receptor subunit beta 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17021187 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:17021187 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17927825 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:9108119 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12475885 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:17927825 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9108119 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:17927825 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:17927825 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:12117532 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:17983671 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:9108119 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17927825 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:9108119 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001400 hyperresponsive IAGP N RGD:5509061 20141003 MGI PMID:9108119 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9108119 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20170921 MGI PMID:26627235 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:17983671 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:9108119 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:9108119 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17927825 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17927825 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:12475885 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:9108119 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:9108119 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0002068 abnormal parental behavior IAGP N RGD:5509061 20141003 MGI PMID:9108119 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9108119 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17927825 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15681950 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:9108119 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20170921 MGI PMID:26627235 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:17983671 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:17983671 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021187 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20141003 MGI PMID:12475885 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20170921 MGI PMID:26627235 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0002911 abnormal inhibitory postsynaptic potential IAGP N RGD:5509061 20170921 MGI PMID:26627235 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:17927825 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:17983671 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0003637 cochlear ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12117532 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0003986 small cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:12117532 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:12117532 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:12475885 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021187 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021187 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0004490 type IV spiral ligament fibrocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021187 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0004632 abnormal cochlear OHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17021187 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0004716 abnormal cochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17021187 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:17021187 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0004746 abnormal cochlear IHC afferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17021187 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20240606 MGI PMID:36192601 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17927825 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17983671 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0005387 immune system phenotype IAGP N RGD:5509061 20240606 MGI PMID:36192601 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:12475885 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:15681950 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0006409 vestibular ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12117532 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20240606 MGI PMID:36192601 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0008397 abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology IAGP N RGD:5509061 20240606 MGI PMID:36192601 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20170921 MGI PMID:26627235 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12475885 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17927825 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20170921 MGI PMID:26627235 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0009957 abnormal cerebellum vermis lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:17983671 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0009989 abnormal cerebellum vermis lobule II morphology IAGP N RGD:5509061 20141003 MGI PMID:17983671 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0009990 abnormal cerebellum vermis lobule III morphology IAGP N RGD:5509061 20141003 MGI PMID:17983671 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0009991 abnormal cerebellum vermis lobule IV morphology IAGP N RGD:5509061 20141003 MGI PMID:17983671 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0009993 abnormal cerebellum vermis lobule V morphology IAGP N RGD:5509061 20141003 MGI PMID:17983671 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0009994 abnormal cerebellum vermis lobule VI morphology IAGP N RGD:5509061 20141003 MGI PMID:17983671 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0009995 abnormal cerebellum vermis lobule VII morphology IAGP N RGD:5509061 20141003 MGI PMID:17983671 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20240606 MGI PMID:36192601 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17927825 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17927825 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17927825 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9108119 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20170921 MGI PMID:26627235 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0011273 prolonged excitatory postsynaptic current decay time IAGP N RGD:5509061 20240418 MGI PMID:26627235 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:17927825 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:17021187 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17021187 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:17021187 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0020335 abnormal dentate gyrus neuron dendrite morphology IAGP N RGD:5509061 20170921 MGI PMID:26627235 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20170921 MGI PMID:26627235 10614 Gabrb3 GABRB3, gamma-aminobutyric acid type A receptor subunit beta 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:17983671 10615 Gad1 glutamate decarboxylase 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10211762 10615 Gad1 glutamate decarboxylase 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17418495 10615 Gad1 glutamate decarboxylase 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:9177246 10615 Gad1 glutamate decarboxylase 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:20096683 10615 Gad1 glutamate decarboxylase 1 gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17582330 10615 Gad1 glutamate decarboxylase 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:9177246 10615 Gad1 glutamate decarboxylase 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:9177246 10615 Gad1 glutamate decarboxylase 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18384748 10615 Gad1 glutamate decarboxylase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18384748 10615 Gad1 glutamate decarboxylase 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20171019 MGI PMID:9326630 10615 Gad1 glutamate decarboxylase 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9326630 10615 Gad1 glutamate decarboxylase 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:18615733 10615 Gad1 glutamate decarboxylase 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:18615733 10615 Gad1 glutamate decarboxylase 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9177246 10615 Gad1 glutamate decarboxylase 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20171019 MGI PMID:9326630 10615 Gad1 glutamate decarboxylase 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17418495 10615 Gad1 glutamate decarboxylase 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9177246 10615 Gad1 glutamate decarboxylase 1 gene MP:0001985 abnormal gustatory system physiology IAGP N RGD:5509061 20141003 MGI PMID:21625513 10615 Gad1 glutamate decarboxylase 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20096683 10615 Gad1 glutamate decarboxylase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10211762 10615 Gad1 glutamate decarboxylase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17582330 10615 Gad1 glutamate decarboxylase 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15654854 10615 Gad1 glutamate decarboxylase 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17418495 10615 Gad1 glutamate decarboxylase 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:20096683 10615 Gad1 glutamate decarboxylase 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:11248119 10615 Gad1 glutamate decarboxylase 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18384748 10615 Gad1 glutamate decarboxylase 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:17418495 10615 Gad1 glutamate decarboxylase 1 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:17418495 10615 Gad1 glutamate decarboxylase 1 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:21625513 10615 Gad1 glutamate decarboxylase 1 gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:15654854 10615 Gad1 glutamate decarboxylase 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:18384748 10615 Gad1 glutamate decarboxylase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20096683 10615 Gad1 glutamate decarboxylase 1 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17582330 10615 Gad1 glutamate decarboxylase 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:20096683 10615 Gad1 glutamate decarboxylase 1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:11248119 10615 Gad1 glutamate decarboxylase 1 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:9326630 10615 Gad1 glutamate decarboxylase 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17376969 10615 Gad1 glutamate decarboxylase 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:20096683 10615 Gad1 glutamate decarboxylase 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20096683 10615 Gad1 glutamate decarboxylase 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:20096683 10615 Gad1 glutamate decarboxylase 1 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:9326630 10615 Gad1 glutamate decarboxylase 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:9177246 10615 Gad1 glutamate decarboxylase 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:20096683 10615 Gad1 glutamate decarboxylase 1 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:20333300 10615 Gad1 glutamate decarboxylase 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:9326630 10615 Gad1 glutamate decarboxylase 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:20333300 10615 Gad1 glutamate decarboxylase 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:9326630 10615 Gad1 glutamate decarboxylase 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:18615733 10615 Gad1 glutamate decarboxylase 1 gene MP:0010146 umbilical hernia IAGP N RGD:5509061 20141003 MGI PMID:20333300 10615 Gad1 glutamate decarboxylase 1 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:17418495 10615 Gad1 glutamate decarboxylase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10211762 10615 Gad1 glutamate decarboxylase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9177246 10615 Gad1 glutamate decarboxylase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9326630 10615 Gad1 glutamate decarboxylase 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17582330 10615 Gad1 glutamate decarboxylase 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18615733 10615 Gad1 glutamate decarboxylase 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10211762 10615 Gad1 glutamate decarboxylase 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17376969 10615 Gad1 glutamate decarboxylase 1 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20161110 MGI PMID:26261347 10615 Gad1 glutamate decarboxylase 1 gene MP:0012595 decreased glutamate decarboxylase activity IAGP N RGD:5509061 20180927 MGI PMID:9177246 10615 Gad1 glutamate decarboxylase 1 gene MP:0030248 narrow maxilla IAGP N RGD:5509061 20171019 MGI PMID:9326630 10615 Gad1 glutamate decarboxylase 1 gene MP:0030733 decreased gamma-aminobutyric acid level IAGP N RGD:5509061 20180927 MGI PMID:10211762 10615 Gad1 glutamate decarboxylase 1 gene MP:0030733 decreased gamma-aminobutyric acid level IAGP N RGD:5509061 20180927 MGI PMID:9177246 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10211762 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17418495 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:10814732 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14676944 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10814732 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20201022 MGI 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:14676944 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17418495 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20170126 MGI PMID:27693255 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10814732 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:14676944 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:8954991 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:9391152 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10211762 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10814732 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14676944 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9391152 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:24027099 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17418495 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:24027099 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20201022 MGI 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:24027099 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:24027099 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20170105 MGI 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:17418495 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0003063 increased coping response IAGP N RGD:5509061 20141003 MGI PMID:10814732 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:17418495 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:10814732 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:10814732 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160421 MGI 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:14676944 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20170105 MGI 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20170105 MGI 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20170126 MGI PMID:27693255 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20170126 MGI PMID:27693255 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20211021 MGI 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:17418495 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10211762 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10211762 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:24027099 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0011987 abnormal GABAergic neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:24027099 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0030733 decreased gamma-aminobutyric acid level IAGP N RGD:5509061 20180927 MGI PMID:10211762 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0030733 decreased gamma-aminobutyric acid level IAGP N RGD:5509061 20180927 MGI PMID:10814732 10616 Gad2 glutamic acid decarboxylase 2 gene MP:0030733 decreased gamma-aminobutyric acid level IAGP N RGD:5509061 20180927 MGI PMID:9391152 10617 Galk1 galactokinase 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:10915771 10617 Galk1 galactokinase 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10915771 10618 Gamt guanidinoacetate methyltransferase gene MP:0000679 increased percent water in carcass IAGP N RGD:5509061 20141003 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0001506 limp posture IAGP N RGD:5509061 20141003 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20180927 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20180927 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0010062 decreased creatine level IAGP N RGD:5509061 20180927 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0010065 decreased circulating creatine level IAGP N RGD:5509061 20180927 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0011468 abnormal urine amino acid level IAGP N RGD:5509061 20141003 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20180927 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:15028668 10618 Gamt guanidinoacetate methyltransferase gene MP:0030633 decreased urine creatine level IAGP N RGD:5509061 20180927 MGI PMID:15028668 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0001304 cataract IEA N RGD:5509061 20221215 MGI 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20230601 MGI 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0002596 abnormal hematocrit IAGP N RGD:5509061 20200310 MGI PMID:17874335 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20221215 MGI 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:17874335 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200310 MGI PMID:3796661 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200310 MGI PMID:3960038 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:17874335 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17874335 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:2040452 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:3796661 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:3960038 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17874335 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17874335 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0011609 decreased glyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity IAGP N RGD:5509061 20200310 MGI PMID:17874335 10619 Gapdh glyceraldehyde-3-phosphate dehydrogenase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 10620 Gast gastrin gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15731364 10620 Gast gastrin gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:12145805 10620 Gast gastrin gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:9287997 10620 Gast gastrin gene MP:0000501 abnormal digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:15735748 10620 Gast gastrin gene MP:0000501 abnormal digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:9530158 10620 Gast gastrin gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:15735748 10620 Gast gastrin gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:15735748 10620 Gast gastrin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15731364 10620 Gast gastrin gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15731364 10620 Gast gastrin gene MP:0003892 abnormal gastric gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11705756 10620 Gast gastrin gene MP:0003892 abnormal gastric gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9530158 10620 Gast gastrin gene MP:0004138 abnormal mucous neck cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9287997 10620 Gast gastrin gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11705756 10620 Gast gastrin gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12388185 10620 Gast gastrin gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9287997 10620 Gast gastrin gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9530158 10620 Gast gastrin gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9287997 10620 Gast gastrin gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20150312 MGI PMID:11705756 10620 Gast gastrin gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:18755804 10620 Gast gastrin gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:12145805 10620 Gast gastrin gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15731364 10620 Gast gastrin gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18755804 10620 Gast gastrin gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20141003 MGI PMID:9287997 10620 Gast gastrin gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12145805 10620 Gast gastrin gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15735748 10620 Gast gastrin gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:11705756 10620 Gast gastrin gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:15735748 10620 Gast gastrin gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:9287997 10620 Gast gastrin gene MP:0011896 increased circulating unsaturated transferrin level IAGP N RGD:5509061 20141003 MGI PMID:18755804 10621 Gata1 GATA binding protein 1 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22354171 10621 Gata1 GATA binding protein 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12045237 10621 Gata1 GATA binding protein 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19682090 10621 Gata1 GATA binding protein 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:9657742 10621 Gata1 GATA binding protein 1 gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17060636 10621 Gata1 GATA binding protein 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19682090 10621 Gata1 GATA binding protein 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17060636 10621 Gata1 GATA binding protein 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22354171 10621 Gata1 GATA binding protein 1 gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14656885 10621 Gata1 GATA binding protein 1 gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:12077323 10621 Gata1 GATA binding protein 1 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:14656885 10621 Gata1 GATA binding protein 1 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:9233806 10621 Gata1 GATA binding protein 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11342429 10621 Gata1 GATA binding protein 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22354171 10621 Gata1 GATA binding protein 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9657742 10621 Gata1 GATA binding protein 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12077323 10621 Gata1 GATA binding protein 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:15175249 10621 Gata1 GATA binding protein 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:15895080 10621 Gata1 GATA binding protein 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:19682090 10621 Gata1 GATA binding protein 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:23717580 10621 Gata1 GATA binding protein 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:8901585 10621 Gata1 GATA binding protein 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:9139715 10621 Gata1 GATA binding protein 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:9576834 10621 Gata1 GATA binding protein 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:9657742 10621 Gata1 GATA binding protein 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:9576834 10621 Gata1 GATA binding protein 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:11342429 10621 Gata1 GATA binding protein 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15895080 10621 Gata1 GATA binding protein 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:15895080 10621 Gata1 GATA binding protein 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:9139715 10621 Gata1 GATA binding protein 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11342429 10621 Gata1 GATA binding protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12045237 10621 Gata1 GATA binding protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22354171 10621 Gata1 GATA binding protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9657742 10621 Gata1 GATA binding protein 1 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:9716588 10621 Gata1 GATA binding protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12077323 10621 Gata1 GATA binding protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15175249 10621 Gata1 GATA binding protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19682090 10621 Gata1 GATA binding protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22354171 10621 Gata1 GATA binding protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8901585 10621 Gata1 GATA binding protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9139715 10621 Gata1 GATA binding protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9233806 10621 Gata1 GATA binding protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9576834 10621 Gata1 GATA binding protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9657742 10621 Gata1 GATA binding protein 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16107690 10621 Gata1 GATA binding protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9139715 10621 Gata1 GATA binding protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9576834 10621 Gata1 GATA binding protein 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:9139715 10621 Gata1 GATA binding protein 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:9139715 10621 Gata1 GATA binding protein 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:9576834 10621 Gata1 GATA binding protein 1 gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:10562540 10621 Gata1 GATA binding protein 1 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:22416124 10621 Gata1 GATA binding protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9657742 10621 Gata1 GATA binding protein 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19682090 10621 Gata1 GATA binding protein 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9576834 10621 Gata1 GATA binding protein 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:15375268 10621 Gata1 GATA binding protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12954777 10621 Gata1 GATA binding protein 1 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:15375268 10621 Gata1 GATA binding protein 1 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:11342429 10621 Gata1 GATA binding protein 1 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:11342429 10621 Gata1 GATA binding protein 1 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:14656885 10621 Gata1 GATA binding protein 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22354171 10621 Gata1 GATA binding protein 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12077323 10621 Gata1 GATA binding protein 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15895080 10621 Gata1 GATA binding protein 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19682090 10621 Gata1 GATA binding protein 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22354171 10621 Gata1 GATA binding protein 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9233806 10621 Gata1 GATA binding protein 1 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:9657742 10621 Gata1 GATA binding protein 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14656885 10621 Gata1 GATA binding protein 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15895080 10621 Gata1 GATA binding protein 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19682090 10621 Gata1 GATA binding protein 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9233806 10621 Gata1 GATA binding protein 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9657742 10621 Gata1 GATA binding protein 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14656885 10621 Gata1 GATA binding protein 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19682090 10621 Gata1 GATA binding protein 1 gene MP:0002596 abnormal hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11342429 10621 Gata1 GATA binding protein 1 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:9233806 10621 Gata1 GATA binding protein 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:14656885 10621 Gata1 GATA binding protein 1 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19682090 10621 Gata1 GATA binding protein 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12045237 10621 Gata1 GATA binding protein 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19682090 10621 Gata1 GATA binding protein 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9576834 10621 Gata1 GATA binding protein 1 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:11342429 10621 Gata1 GATA binding protein 1 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:11342429 10621 Gata1 GATA binding protein 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:14656885 10621 Gata1 GATA binding protein 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:9233806 10621 Gata1 GATA binding protein 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:9657742 10621 Gata1 GATA binding protein 1 gene MP:0003405 abnormal platelet shape IAGP N RGD:5509061 20141003 MGI PMID:11342429 10621 Gata1 GATA binding protein 1 gene MP:0003405 abnormal platelet shape IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:14656885 10621 Gata1 GATA binding protein 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:9576834 10621 Gata1 GATA binding protein 1 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:14656885 10621 Gata1 GATA binding protein 1 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:9139715 10621 Gata1 GATA binding protein 1 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:14656885 10621 Gata1 GATA binding protein 1 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:19682090 10621 Gata1 GATA binding protein 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:15005853 10621 Gata1 GATA binding protein 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:15005853 10621 Gata1 GATA binding protein 1 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12045237 10621 Gata1 GATA binding protein 1 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17060636 10621 Gata1 GATA binding protein 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17060636 10621 Gata1 GATA binding protein 1 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:22416124 10621 Gata1 GATA binding protein 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:19682090 10621 Gata1 GATA binding protein 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:22354171 10621 Gata1 GATA binding protein 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11342429 10621 Gata1 GATA binding protein 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0008247 abnormal mononuclear cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14656885 10621 Gata1 GATA binding protein 1 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14656885 10621 Gata1 GATA binding protein 1 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19682090 10621 Gata1 GATA binding protein 1 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22354171 10621 Gata1 GATA binding protein 1 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9233806 10621 Gata1 GATA binding protein 1 gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:9657742 10621 Gata1 GATA binding protein 1 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:9657742 10621 Gata1 GATA binding protein 1 gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:17060636 10621 Gata1 GATA binding protein 1 gene MP:0008609 decreased circulating interleukin-13 level IAGP N RGD:5509061 20141003 MGI PMID:17060636 10621 Gata1 GATA binding protein 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:9233806 10621 Gata1 GATA binding protein 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:9576834 10621 Gata1 GATA binding protein 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:9657742 10621 Gata1 GATA binding protein 1 gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11342429 10621 Gata1 GATA binding protein 1 gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11342429 10621 Gata1 GATA binding protein 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:11342429 10621 Gata1 GATA binding protein 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:16391009 10621 Gata1 GATA binding protein 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19682090 10621 Gata1 GATA binding protein 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:23717580 10621 Gata1 GATA binding protein 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:9139715 10621 Gata1 GATA binding protein 1 gene MP:0009246 pale spleen IAGP N RGD:5509061 20141003 MGI PMID:9657742 10621 Gata1 GATA binding protein 1 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:11342429 10621 Gata1 GATA binding protein 1 gene MP:0009676 abnormal hemostasis IAGP N RGD:5509061 20141003 MGI PMID:17060636 10621 Gata1 GATA binding protein 1 gene MP:0010178 increased number of Howell-Jolly bodies IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:15005853 10621 Gata1 GATA binding protein 1 gene MP:0010964 increased compact bone volume IAGP N RGD:5509061 20141003 MGI PMID:15005853 10621 Gata1 GATA binding protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12077323 10621 Gata1 GATA binding protein 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12077323 10621 Gata1 GATA binding protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8901585 10621 Gata1 GATA binding protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9139715 10621 Gata1 GATA binding protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9576834 10621 Gata1 GATA binding protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15175249 10621 Gata1 GATA binding protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12077323 10621 Gata1 GATA binding protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9576834 10621 Gata1 GATA binding protein 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9576834 10621 Gata1 GATA binding protein 1 gene MP:0011747 myelofibrosis IAGP N RGD:5509061 20141003 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:16966598 10621 Gata1 GATA binding protein 1 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:12149188 10621 Gata1 GATA binding protein 1 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:15005853 10621 Gata1 GATA binding protein 1 gene MP:0031276 abnormal stress erythropoiesis IAGP N RGD:5509061 20210805 MGI PMID:14656885 10624 Gc vitamin D binding protein gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20170105 MGI 10624 Gc vitamin D binding protein gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20170105 MGI 10624 Gc vitamin D binding protein gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:9916136 10624 Gc vitamin D binding protein gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20170105 MGI 10624 Gc vitamin D binding protein gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:9916136 10624 Gc vitamin D binding protein gene MP:0003432 increased activity of parathyroid IAGP N RGD:5509061 20141003 MGI PMID:9916136 10624 Gc vitamin D binding protein gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:9916136 10624 Gc vitamin D binding protein gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20170105 MGI 10624 Gc vitamin D binding protein gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170105 MGI 10624 Gc vitamin D binding protein gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20231207 MGI 10624 Gc vitamin D binding protein gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:9916136 10626 Gcg glucagon gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:19819987 10626 Gcg glucagon gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19819987 10626 Gcg glucagon gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 10626 Gcg glucagon gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19819987 10626 Gcg glucagon gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:19819987 10626 Gcg glucagon gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19819987 10626 Gcg glucagon gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19819987 10626 Gcg glucagon gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19819987 10626 Gcg glucagon gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19819987 10626 Gcg glucagon gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19819987 10626 Gcg glucagon gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19819987 10626 Gcg glucagon gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:19819987 10626 Gcg glucagon gene MP:0009167 increased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:19819987 10626 Gcg glucagon gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12354782 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18829665 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12354782 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:11027356 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:11027356 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:12354782 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:18829665 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:11027356 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:18829665 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:12354782 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0004494 abnormal synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:18829665 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0004495 decreased synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:18829665 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:18829665 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:12354782 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:12354782 10630 Gdi1 GDP dissociation inhibitor 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:18829665 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:8657308 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:17537792 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:20439720 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:24656820 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:8657306 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:8657307 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:8657308 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:12574104 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:15691764 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:24656820 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:8657307 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:15130495 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000836 abnormal substantia nigra morphology IAGP N RGD:5509061 20141003 MGI PMID:18536709 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:18305247 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19954518 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:8657306 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:18305247 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:8657308 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8657306 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19954518 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:12668632 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:11774071 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:12668632 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12668632 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0001047 abnormal enteric cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8657307 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:8657306 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:8657307 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:8657308 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:12372284 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:16600854 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12372284 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:8657308 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18536709 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17537792 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:8657307 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:18536709 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:8657308 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12574104 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:11774071 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0002827 abnormal renal corpuscle morphology IAGP N RGD:5509061 20141003 MGI PMID:11422733 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0002827 abnormal renal corpuscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12574104 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0002955 increased compensatory renal growth IAGP N RGD:5509061 20141003 MGI PMID:20943767 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:11422733 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:17537792 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:24656820 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:8657307 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20943767 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003268 chronic constipation IAGP N RGD:5509061 20141003 MGI PMID:11774071 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:11774071 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:12668632 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:8657307 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003307 pyloric stenosis IAGP N RGD:5509061 20141003 MGI PMID:8657306 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003437 abnormal carotid body morphology IAGP N RGD:5509061 20141003 MGI PMID:18536709 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20439720 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8657308 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:11422733 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:11774071 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:20943767 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:8657306 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:8657307 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:8657308 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18536709 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:8657308 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:11422733 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:20943767 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:18305247 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:18536709 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0004103 abnormal ventral striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:18536709 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:11422733 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:12574104 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:24656820 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12574104 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:11422733 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:8657307 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20943767 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:12668632 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:8657307 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0006100 abnormal tegmentum morphology IAGP N RGD:5509061 20141003 MGI PMID:18536709 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:20943767 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0009511 distended stomach IAGP N RGD:5509061 20141003 MGI PMID:11774071 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0009684 abnormal spinal cord lateral motor column morphology IAGP N RGD:5509061 20141003 MGI PMID:12372284 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0010800 abnormal submucous nerve plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:11774071 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0010801 abnormal myenteric nerve plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:11774071 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:8657306 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:8657307 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:8657308 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:8657306 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:8657308 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8657306 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8657307 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8657308 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11774071 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:11422733 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:12574104 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:20943767 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12574104 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20943767 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011359 decreased glomerular capillary number IAGP N RGD:5509061 20141003 MGI PMID:20943767 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:12574104 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:20943767 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:20943767 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20943767 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20943767 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20141003 MGI PMID:20943767 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0011881 distended duodenum IAGP N RGD:5509061 20150702 MGI PMID:8657306 10631 Gdnf glial cell line derived neurotrophic factor gene MP:0020491 abnormal ovary topology IAGP N RGD:5509061 20171026 MGI PMID:8657308 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22932805 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15252036 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22932805 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:22932805 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:17116877 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:15252036 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22932805 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17116877 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22393124 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17116877 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17116877 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15254021 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001967 deafness IAGP N RGD:5509061 20170907 MGI PMID:26469318 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0001967 deafness IAGP N RGD:5509061 20191212 MGI PMID:29961578 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22932805 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17116877 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22932805 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15252036 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201217 MGI PMID:31077553 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0002620 abnormal monocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0002623 abnormal vestibular hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:17116877 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:22932805 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004327 increased vestibular hair cell number IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15254021 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20170907 MGI PMID:26469318 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20191212 MGI PMID:29961578 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15254021 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20170907 MGI PMID:26469318 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004403 absent cochlear outer hair cells IAGP N RGD:5509061 20170907 MGI PMID:26469318 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15254021 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20170907 MGI PMID:26469318 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15254021 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004530 absent outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15254021 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004536 short inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:15254021 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004589 abnormal cochlear hair cell development IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004632 abnormal cochlear OHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15254021 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22932805 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20826720 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17116877 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22932805 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17116877 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:17116877 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20170907 MGI PMID:26469318 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0006325 impaired hearing IAGP N RGD:5509061 20170907 MGI PMID:26469318 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:12441305 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22393124 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0008112 abnormal monocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:11810106 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0008791 decreased NK cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:22393124 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22932805 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22393124 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0011061 abnormal inner hair cell kinocilium morphology IAGP N RGD:5509061 20170907 MGI PMID:26469318 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20191219 MGI PMID:31444330 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0011689 absent neutrophils IAGP N RGD:5509061 20141003 MGI PMID:22393124 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16397623 10634 Gfi1 growth factor independent 1 transcription repressor gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20063299 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:17507417 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000392 accelerated hair follicle regression IAGP N RGD:5509061 20141003 MGI PMID:10702420 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10682708 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10682708 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:10682708 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:15541311 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:17507417 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:23542432 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:9728913 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:10682708 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:10682708 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:9728913 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15541311 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19954518 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:19954518 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:12372284 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:18305247 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19954518 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:18305247 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001033 abnormal parasympathetic system morphology IAGP N RGD:5509061 20141003 MGI PMID:11069590 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19954518 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:10682708 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17507417 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:9728913 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:17507417 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:9728913 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12668632 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9697851 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:15541311 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:17507417 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:9697851 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:12372284 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9697851 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12372284 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9697851 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:9697851 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001087 abnormal nodose ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9697851 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:10702420 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:10682708 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:9697851 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:9728913 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15541311 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:9697851 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:23542432 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20230615 MGI PMID:17507417 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:9697851 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:12668632 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0003585 large ureter IAGP N RGD:5509061 20141003 MGI PMID:23542432 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:23542432 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:15541311 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:10682708 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:9697851 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:9697851 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:17507417 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:18305247 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:15541311 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:17507417 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:12668632 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:23542432 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:9728913 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:17322904 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0008314 abnormal pterygopalatine ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11069590 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0008315 abnormal otic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11069590 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0009684 abnormal spinal cord lateral motor column morphology IAGP N RGD:5509061 20141003 MGI PMID:12372284 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:9697851 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0010981 abnormal branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:23542432 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:9728913 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10682708 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17507417 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9728913 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9697851 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15541311 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0011292 absent nephron IAGP N RGD:5509061 20141003 MGI PMID:9697851 10635 Gfra1 glial cell line derived neurotrophic factor family receptor alpha 1 gene MP:0011760 abnormal ureteric bud tip morphology IAGP N RGD:5509061 20141003 MGI PMID:23542432 10636 Ggh gamma-glutamyl hydrolase gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 10636 Ggh gamma-glutamyl hydrolase gene MP:0002637 small uterus IEA N RGD:5509061 20220519 MGI 10636 Ggh gamma-glutamyl hydrolase gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12714507 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12714507 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12714507 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12714507 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9155011 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9155011 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:11900463 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12714507 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:9155011 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20141003 MGI PMID:9155011 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:9155011 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:9155011 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:9155011 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9155011 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9155011 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:9155011 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9155011 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9155011 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0002293 long gestation period IAGP N RGD:5509061 20141003 MGI PMID:9374408 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:12714507 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:12714507 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:12714507 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20190613 MGI PMID:17255313 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:9374408 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20190613 MGI PMID:17255313 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20190613 MGI PMID:17255313 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:12714507 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12714507 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:15039218 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:15039218 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15039218 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:11900463 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:9155011 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0004514 dystocia IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:9374408 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:9374408 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:12714507 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:9155011 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12714507 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:12714507 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0005161 hematuria IAGP N RGD:5509061 20190613 MGI PMID:17255313 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20190613 MGI PMID:17255313 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20190613 MGI PMID:17255313 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0005410 abnormal fertilization IAGP N RGD:5509061 20141003 MGI PMID:9374408 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11900463 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:9374408 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:12714507 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:11900463 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0008294 abnormal adrenal gland zona fasciculata morphology IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0008295 abnormal adrenal gland zona reticularis morphology IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:15039218 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9155011 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9374408 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20190613 MGI PMID:17255313 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20190613 MGI PMID:17255313 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0013337 abnormal adenohypophysis development IAGP N RGD:5509061 20141211 MGI PMID:9013935 10640 B4galt1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 gene MP:0020180 abnormal IgM level IAGP N RGD:5509061 20190613 MGI PMID:17255313 10643 Gh growth hormone gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:14726450 10643 Gh growth hormone gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:14726450 10643 Gh growth hormone gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 10643 Gh growth hormone gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 10643 Gh growth hormone gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:14726450 10643 Gh growth hormone gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20170105 MGI 10643 Gh growth hormone gene MP:0000692 small spleen IEA N RGD:5509061 20170105 MGI 10643 Gh growth hormone gene MP:0001258 decreased body length IEA N RGD:5509061 20210520 MGI 10643 Gh growth hormone gene MP:0001262 decreased body weight IEA N RGD:5509061 20190530 MGI 10643 Gh growth hormone gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 10643 Gh growth hormone gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:14726450 10643 Gh growth hormone gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:14726450 10643 Gh growth hormone gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 10643 Gh growth hormone gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 10643 Gh growth hormone gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:14726450 10643 Gh growth hormone gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170105 MGI 10643 Gh growth hormone gene MP:0002175 decreased brain weight IEA N RGD:5509061 20220519 MGI 10643 Gh growth hormone gene MP:0002188 small heart IEA N RGD:5509061 20170105 MGI 10643 Gh growth hormone gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:14726450 10643 Gh growth hormone gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:14726450 10643 Gh growth hormone gene MP:0002834 decreased heart weight IEA N RGD:5509061 20201022 MGI 10643 Gh growth hormone gene MP:0002989 small kidney IEA N RGD:5509061 20170105 MGI 10643 Gh growth hormone gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20231207 MGI 10643 Gh growth hormone gene MP:0003402 decreased liver weight IEA N RGD:5509061 20220519 MGI 10643 Gh growth hormone gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 10643 Gh growth hormone gene MP:0003918 decreased kidney weight IEA N RGD:5509061 20210128 MGI 10643 Gh growth hormone gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20231207 MGI 10643 Gh growth hormone gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141127 MGI PMID:14726450 10643 Gh growth hormone gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20210128 MGI 10643 Gh growth hormone gene MP:0004956 decreased thymus weight IEA N RGD:5509061 20220519 MGI 10643 Gh growth hormone gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20160421 MGI 10643 Gh growth hormone gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141127 MGI PMID:14726450 10643 Gh growth hormone gene MP:0005631 decreased lung weight IEA N RGD:5509061 20220519 MGI 10643 Gh growth hormone gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:14726450 10643 Gh growth hormone gene MP:0008330 absent somatotrophs IAGP N RGD:5509061 20141127 MGI PMID:14726450 10643 Gh growth hormone gene MP:0008333 absent lactotrophs IAGP N RGD:5509061 20141127 MGI PMID:14726450 10643 Gh growth hormone gene MP:0008938 decreased pituitary gland weight IAGP N RGD:5509061 20141127 MGI PMID:14726450 10643 Gh growth hormone gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 10643 Gh growth hormone gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20231207 MGI 10643 Gh growth hormone gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160811 MGI 10643 Gh growth hormone gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 10643 Gh growth hormone gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 10643 Gh growth hormone gene MP:0011612 increased circulating ghrelin level IAGP N RGD:5509061 20141003 MGI PMID:14726450 10643 Gh growth hormone gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 10644 Ghr growth hormone receptor gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15231300 10644 Ghr growth hormone receptor gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19460757 10644 Ghr growth hormone receptor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11133160 10644 Ghr growth hormone receptor gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11133160 10644 Ghr growth hormone receptor gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11133160 10644 Ghr growth hormone receptor gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:11133160 10644 Ghr growth hormone receptor gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:15601831 10644 Ghr growth hormone receptor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:12297526 10644 Ghr growth hormone receptor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12185100 10644 Ghr growth hormone receptor gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:9371826 10644 Ghr growth hormone receptor gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:10875265 10644 Ghr growth hormone receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10067829 10644 Ghr growth hormone receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10875265 10644 Ghr growth hormone receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10974652 10644 Ghr growth hormone receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12185100 10644 Ghr growth hormone receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15231300 10644 Ghr growth hormone receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19884384 10644 Ghr growth hormone receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10875265 10644 Ghr growth hormone receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19460757 10644 Ghr growth hormone receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9371826 10644 Ghr growth hormone receptor gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 10644 Ghr growth hormone receptor gene MP:0001462 abnormal avoidance learning behavior IAGP N RGD:5509061 20141003 MGI PMID:11336996 10644 Ghr growth hormone receptor gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19460757 10644 Ghr growth hormone receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15601831 10644 Ghr growth hormone receptor gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:10875265 10644 Ghr growth hormone receptor gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:12297526 10644 Ghr growth hormone receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10875265 10644 Ghr growth hormone receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11133160 10644 Ghr growth hormone receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15601831 10644 Ghr growth hormone receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19460757 10644 Ghr growth hormone receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9371826 10644 Ghr growth hormone receptor gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:11395925 10644 Ghr growth hormone receptor gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10067829 10644 Ghr growth hormone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12297526 10644 Ghr growth hormone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11133160 10644 Ghr growth hormone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12297526 10644 Ghr growth hormone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9371826 10644 Ghr growth hormone receptor gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:10342852 10644 Ghr growth hormone receptor gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:11133160 10644 Ghr growth hormone receptor gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:12185100 10644 Ghr growth hormone receptor gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20240613 MGI PMID:12297526 10644 Ghr growth hormone receptor gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:11336996 10644 Ghr growth hormone receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19460757 10644 Ghr growth hormone receptor gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:15231300 10644 Ghr growth hormone receptor gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:15601831 10644 Ghr growth hormone receptor gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:19884384 10644 Ghr growth hormone receptor gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:19269870 10644 Ghr growth hormone receptor gene MP:0002293 long gestation period IAGP N RGD:5509061 20141003 MGI PMID:10342852 10644 Ghr growth hormone receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19460757 10644 Ghr growth hormone receptor gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:10342852 10644 Ghr growth hormone receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19460757 10644 Ghr growth hormone receptor gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:12297526 10644 Ghr growth hormone receptor gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:12297526 10644 Ghr growth hormone receptor gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10974652 10644 Ghr growth hormone receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11395925 10644 Ghr growth hormone receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:10067829 10644 Ghr growth hormone receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:10067829 10644 Ghr growth hormone receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:12185100 10644 Ghr growth hormone receptor gene MP:0002782 abnormal testes secretion IAGP N RGD:5509061 20141003 MGI PMID:12185100 10644 Ghr growth hormone receptor gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19269870 10644 Ghr growth hormone receptor gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:10974652 10644 Ghr growth hormone receptor gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0002965 increased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19460757 10644 Ghr growth hormone receptor gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:11133160 10644 Ghr growth hormone receptor gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:15601831 10644 Ghr growth hormone receptor gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:21555853 10644 Ghr growth hormone receptor gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:12297526 10644 Ghr growth hormone receptor gene MP:0003356 impaired luteinization IAGP N RGD:5509061 20141003 MGI PMID:12297526 10644 Ghr growth hormone receptor gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:15601831 10644 Ghr growth hormone receptor gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19884384 10644 Ghr growth hormone receptor gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11133160 10644 Ghr growth hormone receptor gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11133160 10644 Ghr growth hormone receptor gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:11395925 10644 Ghr growth hormone receptor gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20141003 MGI PMID:12297526 10644 Ghr growth hormone receptor gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:11133160 10644 Ghr growth hormone receptor gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:15231300 10644 Ghr growth hormone receptor gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:19460757 10644 Ghr growth hormone receptor gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:10342852 10644 Ghr growth hormone receptor gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10342852 10644 Ghr growth hormone receptor gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:19884384 10644 Ghr growth hormone receptor gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:10067829 10644 Ghr growth hormone receptor gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:10875265 10644 Ghr growth hormone receptor gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:11133160 10644 Ghr growth hormone receptor gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:15601831 10644 Ghr growth hormone receptor gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:19460757 10644 Ghr growth hormone receptor gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:19884384 10644 Ghr growth hormone receptor gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:9371826 10644 Ghr growth hormone receptor gene MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10614635 10644 Ghr growth hormone receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10067829 10644 Ghr growth hormone receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12185100 10644 Ghr growth hormone receptor gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:10342852 10644 Ghr growth hormone receptor gene MP:0004908 abnormal seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:12185100 10644 Ghr growth hormone receptor gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:10067829 10644 Ghr growth hormone receptor gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:12185100 10644 Ghr growth hormone receptor gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:10342852 10644 Ghr growth hormone receptor gene MP:0004927 abnormal epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:12185100 10644 Ghr growth hormone receptor gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:12185100 10644 Ghr growth hormone receptor gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:11133160 10644 Ghr growth hormone receptor gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:19460757 10644 Ghr growth hormone receptor gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:19884384 10644 Ghr growth hormone receptor gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:9371826 10644 Ghr growth hormone receptor gene MP:0005124 increased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:10067829 10644 Ghr growth hormone receptor gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:12297526 10644 Ghr growth hormone receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19460757 10644 Ghr growth hormone receptor gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:15231300 10644 Ghr growth hormone receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:19884384 10644 Ghr growth hormone receptor gene MP:0005473 decreased triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:11395925 10644 Ghr growth hormone receptor gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:11395925 10644 Ghr growth hormone receptor gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:11395925 10644 Ghr growth hormone receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21555853 10644 Ghr growth hormone receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10974652 10644 Ghr growth hormone receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11395925 10644 Ghr growth hormone receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20240523 MGI 10644 Ghr growth hormone receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19269870 10644 Ghr growth hormone receptor gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:12185100 10644 Ghr growth hormone receptor gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0008938 decreased pituitary gland weight IAGP N RGD:5509061 20141003 MGI PMID:10067829 10644 Ghr growth hormone receptor gene MP:0008940 delayed balanopreputial separation IAGP N RGD:5509061 20141003 MGI PMID:12185100 10644 Ghr growth hormone receptor gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:11133160 10644 Ghr growth hormone receptor gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:9371826 10644 Ghr growth hormone receptor gene MP:0008975 delayed male fertility IAGP N RGD:5509061 20141003 MGI PMID:12297526 10644 Ghr growth hormone receptor gene MP:0008976 delayed female fertility IAGP N RGD:5509061 20141003 MGI PMID:9371826 10644 Ghr growth hormone receptor gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:12297526 10644 Ghr growth hormone receptor gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:12297526 10644 Ghr growth hormone receptor gene MP:0009019 abnormal metestrus IAGP N RGD:5509061 20141003 MGI PMID:12297526 10644 Ghr growth hormone receptor gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:21555853 10644 Ghr growth hormone receptor gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20200402 MGI PMID:31806625 10644 Ghr growth hormone receptor gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15601831 10644 Ghr growth hormone receptor gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19884384 10644 Ghr growth hormone receptor gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19884384 10644 Ghr growth hormone receptor gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15231300 10644 Ghr growth hormone receptor gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19460757 10644 Ghr growth hormone receptor gene MP:0009425 increased soleus weight IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:10342852 10644 Ghr growth hormone receptor gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:10342852 10644 Ghr growth hormone receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15601831 10644 Ghr growth hormone receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20200402 MGI PMID:31806625 10644 Ghr growth hormone receptor gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:15138153 10644 Ghr growth hormone receptor gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9371826 10644 Ghr growth hormone receptor gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10342852 10644 Ghr growth hormone receptor gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9371826 10644 Ghr growth hormone receptor gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20150611 MGI PMID:21555853 10644 Ghr growth hormone receptor gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20200402 MGI PMID:31806625 10644 Ghr growth hormone receptor gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:16174655 10644 Ghr growth hormone receptor gene MP:0013618 decreased areal bone mineral density IAGP N RGD:5509061 20150319 MGI PMID:10631109 10644 Ghr growth hormone receptor gene MP:0014269 decreased testes secretion IAGP N RGD:5509061 20230810 MGI PMID:10067829 10644 Ghr growth hormone receptor gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:23349524 10644 Ghr growth hormone receptor gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:15231300 10644 Ghr growth hormone receptor gene MP:0031362 decreased prostate gland ventral lobe weight IAGP N RGD:5509061 20220303 MGI PMID:10067829 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0001258 decreased body length IEA N RGD:5509061 20160421 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12537301 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18063435 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12388430 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210520 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:12537301 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:978118 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:1270792 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:1270792 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:1270792 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:978118 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20160421 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0002834 decreased heart weight IEA N RGD:5509061 20170105 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210520 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0003194 abnormal frequency of paradoxical sleep IAGP N RGD:5509061 20141003 MGI PMID:12388430 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:1270792 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20141003 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:12537301 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:18063435 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12960295 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:7679139 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:1270792 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0005138 decreased prolactin level IAGP N RGD:5509061 20141003 MGI PMID:1270792 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:12537301 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:1270792 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:18063435 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0008156 decreased diameter of tibia IAGP N RGD:5509061 20220922 MGI PMID:18063435 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0008322 abnormal somatotroph morphology IAGP N RGD:5509061 20141003 MGI PMID:6194978 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0008329 decreased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:6194978 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0008417 decreased somatotroph cell size IAGP N RGD:5509061 20141003 MGI PMID:6194978 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0008436 decreased somatotroph secretory granule number IAGP N RGD:5509061 20141003 MGI PMID:6194978 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0008437 absent somatotroph secretory granules IAGP N RGD:5509061 20141003 MGI PMID:6194978 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0008831 abnormal insulin-like growth factor I level IEA N RGD:5509061 20141003 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:978118 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15388648 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:7679139 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0010052 increased grip strength IEA N RGD:5509061 20170105 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0010119 abnormal bone mineral density IEA N RGD:5509061 20141003 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160421 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20160421 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0013615 increased volumetric bone mineral density IAGP N RGD:5509061 20220922 MGI PMID:18063435 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0013616 decreased volumetric bone mineral density IEA N RGD:5509061 20150319 MGI 10645 Ghrhr growth hormone releasing hormone receptor gene MP:0020010 decreased bone mineral density of femur IEA N RGD:5509061 20141003 MGI 10649 Gja1 gap junction protein, alpha 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0000126 brittle teeth IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15548583 10649 Gja1 gap junction protein, alpha 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:9118799 10649 Gja1 gap junction protein, alpha 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16624854 10649 Gja1 gap junction protein, alpha 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:17644066 10649 Gja1 gap junction protein, alpha 1 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9118799 10649 Gja1 gap junction protein, alpha 1 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:15282340 10649 Gja1 gap junction protein, alpha 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:15548583 10649 Gja1 gap junction protein, alpha 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0000448 pointed snout IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:18077386 10649 Gja1 gap junction protein, alpha 1 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:15601660 10649 Gja1 gap junction protein, alpha 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0000884 delaminated Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0000887 delaminated cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:19259389 10649 Gja1 gap junction protein, alpha 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:10208994 10649 Gja1 gap junction protein, alpha 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:10208994 10649 Gja1 gap junction protein, alpha 1 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220407 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15282340 10649 Gja1 gap junction protein, alpha 1 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:15282340 10649 Gja1 gap junction protein, alpha 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:15282340 10649 Gja1 gap junction protein, alpha 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:10208994 10649 Gja1 gap junction protein, alpha 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17591950 10649 Gja1 gap junction protein, alpha 1 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:17591950 10649 Gja1 gap junction protein, alpha 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:17591950 10649 Gja1 gap junction protein, alpha 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17591950 10649 Gja1 gap junction protein, alpha 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:15282340 10649 Gja1 gap junction protein, alpha 1 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:15282340 10649 Gja1 gap junction protein, alpha 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:15282340 10649 Gja1 gap junction protein, alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16449318 10649 Gja1 gap junction protein, alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9109444 10649 Gja1 gap junction protein, alpha 1 gene MP:0001443 poor grooming IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11481448 10649 Gja1 gap junction protein, alpha 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:9109444 10649 Gja1 gap junction protein, alpha 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:7892609 10649 Gja1 gap junction protein, alpha 1 gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:11481448 10649 Gja1 gap junction protein, alpha 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:21527737 10649 Gja1 gap junction protein, alpha 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:14967725 10649 Gja1 gap junction protein, alpha 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:23558439 10649 Gja1 gap junction protein, alpha 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16449318 10649 Gja1 gap junction protein, alpha 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:7892609 10649 Gja1 gap junction protein, alpha 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21807945 10649 Gja1 gap junction protein, alpha 1 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:19259389 10649 Gja1 gap junction protein, alpha 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:19259389 10649 Gja1 gap junction protein, alpha 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17591950 10649 Gja1 gap junction protein, alpha 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15282340 10649 Gja1 gap junction protein, alpha 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19259389 10649 Gja1 gap junction protein, alpha 1 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:7892609 10649 Gja1 gap junction protein, alpha 1 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16624854 10649 Gja1 gap junction protein, alpha 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9118799 10649 Gja1 gap junction protein, alpha 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11179202 10649 Gja1 gap junction protein, alpha 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23558439 10649 Gja1 gap junction protein, alpha 1 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:9118799 10649 Gja1 gap junction protein, alpha 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11135457 10649 Gja1 gap junction protein, alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11481448 10649 Gja1 gap junction protein, alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16449318 10649 Gja1 gap junction protein, alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16703618 10649 Gja1 gap junction protein, alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:22135478 10649 Gja1 gap junction protein, alpha 1 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:15282340 10649 Gja1 gap junction protein, alpha 1 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:23558439 10649 Gja1 gap junction protein, alpha 1 gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10208994 10649 Gja1 gap junction protein, alpha 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0002336 abnormal pulmonary gas exchange IAGP N RGD:5509061 20141003 MGI PMID:7892609 10649 Gja1 gap junction protein, alpha 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17038639 10649 Gja1 gap junction protein, alpha 1 gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11179202 10649 Gja1 gap junction protein, alpha 1 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:14967725 10649 Gja1 gap junction protein, alpha 1 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:19259389 10649 Gja1 gap junction protein, alpha 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0002748 abnormal pulmonary valve morphology IAGP N RGD:5509061 20141003 MGI PMID:7892609 10649 Gja1 gap junction protein, alpha 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15282340 10649 Gja1 gap junction protein, alpha 1 gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0002776 increased Sertoli cell number IAGP N RGD:5509061 20141003 MGI PMID:17591950 10649 Gja1 gap junction protein, alpha 1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17591950 10649 Gja1 gap junction protein, alpha 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:12840073 10649 Gja1 gap junction protein, alpha 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:15282340 10649 Gja1 gap junction protein, alpha 1 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21527737 10649 Gja1 gap junction protein, alpha 1 gene MP:0003108 short zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:14967725 10649 Gja1 gap junction protein, alpha 1 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:18077386 10649 Gja1 gap junction protein, alpha 1 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:21527737 10649 Gja1 gap junction protein, alpha 1 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:9109444 10649 Gja1 gap junction protein, alpha 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:15282340 10649 Gja1 gap junction protein, alpha 1 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0003356 impaired luteinization IAGP N RGD:5509061 20141003 MGI PMID:15282340 10649 Gja1 gap junction protein, alpha 1 gene MP:0003390 lymphedema IAGP N RGD:5509061 20141003 MGI PMID:21807945 10649 Gja1 gap junction protein, alpha 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18958191 10649 Gja1 gap junction protein, alpha 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0003838 abnormal milk ejection IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:16624854 10649 Gja1 gap junction protein, alpha 1 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0003900 shortened QT interval IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0003930 abnormal tooth hard tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:15548583 10649 Gja1 gap junction protein, alpha 1 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:16624854 10649 Gja1 gap junction protein, alpha 1 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:7892609 10649 Gja1 gap junction protein, alpha 1 gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:16449318 10649 Gja1 gap junction protein, alpha 1 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15548583 10649 Gja1 gap junction protein, alpha 1 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16624854 10649 Gja1 gap junction protein, alpha 1 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16802337 10649 Gja1 gap junction protein, alpha 1 gene MP:0004116 abnormal atrioventricular bundle conduction IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:18077386 10649 Gja1 gap junction protein, alpha 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:23558439 10649 Gja1 gap junction protein, alpha 1 gene MP:0004225 patent cardiac foramen ovale IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0004385 interparietal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0004540 small maxilla IAGP N RGD:5509061 20171026 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20170914 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17591950 10649 Gja1 gap junction protein, alpha 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141009 MGI PMID:22652908 10649 Gja1 gap junction protein, alpha 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:11514348 10649 Gja1 gap junction protein, alpha 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:17591950 10649 Gja1 gap junction protein, alpha 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16449318 10649 Gja1 gap junction protein, alpha 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:17591950 10649 Gja1 gap junction protein, alpha 1 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11481448 10649 Gja1 gap junction protein, alpha 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15282340 10649 Gja1 gap junction protein, alpha 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16449318 10649 Gja1 gap junction protein, alpha 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11481448 10649 Gja1 gap junction protein, alpha 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141009 MGI PMID:22652908 10649 Gja1 gap junction protein, alpha 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0006049 semilunar valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:15548583 10649 Gja1 gap junction protein, alpha 1 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0006110 ventricular fibrillation IAGP N RGD:5509061 20141003 MGI PMID:23558439 10649 Gja1 gap junction protein, alpha 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:16624854 10649 Gja1 gap junction protein, alpha 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:23558439 10649 Gja1 gap junction protein, alpha 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:7892609 10649 Gja1 gap junction protein, alpha 1 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11481448 10649 Gja1 gap junction protein, alpha 1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:17591950 10649 Gja1 gap junction protein, alpha 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17591950 10649 Gja1 gap junction protein, alpha 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19259389 10649 Gja1 gap junction protein, alpha 1 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:18077386 10649 Gja1 gap junction protein, alpha 1 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:23558439 10649 Gja1 gap junction protein, alpha 1 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11481448 10649 Gja1 gap junction protein, alpha 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:16624854 10649 Gja1 gap junction protein, alpha 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:16624854 10649 Gja1 gap junction protein, alpha 1 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0010194 absent lymphatic vessels IAGP N RGD:5509061 20141003 MGI PMID:21807945 10649 Gja1 gap junction protein, alpha 1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:16449318 10649 Gja1 gap junction protein, alpha 1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:23558439 10649 Gja1 gap junction protein, alpha 1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:9109444 10649 Gja1 gap junction protein, alpha 1 gene MP:0010394 decreased QRS amplitude IAGP N RGD:5509061 20141003 MGI PMID:16449318 10649 Gja1 gap junction protein, alpha 1 gene MP:0010394 decreased QRS amplitude IAGP N RGD:5509061 20141003 MGI PMID:18077386 10649 Gja1 gap junction protein, alpha 1 gene MP:0010428 abnormal heart right ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:16449318 10649 Gja1 gap junction protein, alpha 1 gene MP:0010428 abnormal heart right ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:16624854 10649 Gja1 gap junction protein, alpha 1 gene MP:0010428 abnormal heart right ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:7892609 10649 Gja1 gap junction protein, alpha 1 gene MP:0010449 heart right ventricle outflow tract stenosis IAGP N RGD:5509061 20141003 MGI PMID:16449318 10649 Gja1 gap junction protein, alpha 1 gene MP:0010453 abnormal coronary vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15548583 10649 Gja1 gap junction protein, alpha 1 gene MP:0010472 abnormal ascending aorta and coronary artery attachment IAGP N RGD:5509061 20141003 MGI PMID:16624854 10649 Gja1 gap junction protein, alpha 1 gene MP:0010476 coronary fistula IAGP N RGD:5509061 20141003 MGI PMID:15548583 10649 Gja1 gap junction protein, alpha 1 gene MP:0010477 coronary artery aneurysm IAGP N RGD:5509061 20141003 MGI PMID:15548583 10649 Gja1 gap junction protein, alpha 1 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:18077386 10649 Gja1 gap junction protein, alpha 1 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:23558439 10649 Gja1 gap junction protein, alpha 1 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15548583 10649 Gja1 gap junction protein, alpha 1 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20141003 MGI PMID:15548583 10649 Gja1 gap junction protein, alpha 1 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:15548583 10649 Gja1 gap junction protein, alpha 1 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16449318 10649 Gja1 gap junction protein, alpha 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15282340 10649 Gja1 gap junction protein, alpha 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16624854 10649 Gja1 gap junction protein, alpha 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11135457 10649 Gja1 gap junction protein, alpha 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23558439 10649 Gja1 gap junction protein, alpha 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7892609 10649 Gja1 gap junction protein, alpha 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17644066 10649 Gja1 gap junction protein, alpha 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16449318 10649 Gja1 gap junction protein, alpha 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21807945 10649 Gja1 gap junction protein, alpha 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18077386 10649 Gja1 gap junction protein, alpha 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17408477 10649 Gja1 gap junction protein, alpha 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18077386 10649 Gja1 gap junction protein, alpha 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:17311295 10649 Gja1 gap junction protein, alpha 1 gene MP:0011919 abnormal R wave IAGP N RGD:5509061 20141003 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20200130 MGI PMID:19259389 10649 Gja1 gap junction protein, alpha 1 gene MP:0013781 abnormal mammary gland luminal epithelium morphology IAGP N RGD:5509061 20150625 MGI PMID:10996788 10649 Gja1 gap junction protein, alpha 1 gene MP:0021160 decreased heart right ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:16624854 10649 Gja1 gap junction protein, alpha 1 gene MP:0030034 depressed nasal bridge IAGP N RGD:5509061 20170914 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0030064 small face IAGP N RGD:5509061 20170921 MGI PMID:18003637 10649 Gja1 gap junction protein, alpha 1 gene MP:0030080 small lower incisors IAGP N RGD:5509061 20170928 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0030190 small snout IAGP N RGD:5509061 20171019 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0030281 thin parietal bone IAGP N RGD:5509061 20171102 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0030315 small neurocranium IAGP N RGD:5509061 20171109 MGI PMID:11076975 10649 Gja1 gap junction protein, alpha 1 gene MP:0031018 decreased granulosa cell proliferation IAGP N RGD:5509061 20200130 MGI PMID:19259389 10649 Gja1 gap junction protein, alpha 1 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:19259389 10649 Gja1 gap junction protein, alpha 1 gene MP:0031508 abnormal vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:22652908 10649 Gja1 gap junction protein, alpha 1 gene MP:0031526 thin right ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:15548583 10649 Gja1 gap junction protein, alpha 1 gene MP:0031584 thick semilunar valve IAGP N RGD:5509061 20240125 MGI PMID:15548583 10649 Gja1 gap junction protein, alpha 1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:16155213 10649 Gja1 gap junction protein, alpha 1 gene MP:0031634 decreased heart right ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:16155213 10650 Gla galactosidase, alpha gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9122231 10650 Gla galactosidase, alpha gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:9122231 10650 Gla galactosidase, alpha gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:22574107 10650 Gla galactosidase, alpha gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:22574107 10650 Gla galactosidase, alpha gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:9122231 10650 Gla galactosidase, alpha gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:22574107 10650 Gla galactosidase, alpha gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:22574107 10650 Gla galactosidase, alpha gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:22574107 10650 Gla galactosidase, alpha gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:22574107 10650 Gla galactosidase, alpha gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22574107 10650 Gla galactosidase, alpha gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20141003 MGI PMID:22574107 10650 Gla galactosidase, alpha gene MP:0010574 dilated aorta IAGP N RGD:5509061 20141003 MGI PMID:22574107 10650 Gla galactosidase, alpha gene MP:0011556 increased urine beta2-microglobulin level IAGP N RGD:5509061 20141003 MGI PMID:24094090 10650 Gla galactosidase, alpha gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:24094090 10651 Glb1 galactosidase, beta 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:10861297 10651 Glb1 galactosidase, beta 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:10861297 10651 Glb1 galactosidase, beta 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11578847 10651 Glb1 galactosidase, beta 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10861297 10651 Glb1 galactosidase, beta 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9063740 10651 Glb1 galactosidase, beta 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:15687347 10651 Glb1 galactosidase, beta 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11578847 10651 Glb1 galactosidase, beta 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:10861297 10651 Glb1 galactosidase, beta 1 gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9063740 10651 Glb1 galactosidase, beta 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9063740 10651 Glb1 galactosidase, beta 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:10861297 10651 Glb1 galactosidase, beta 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10861297 10651 Glb1 galactosidase, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10861297 10651 Glb1 galactosidase, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9063740 10651 Glb1 galactosidase, beta 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9071485 10651 Glb1 galactosidase, beta 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:11578847 10651 Glb1 galactosidase, beta 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:10861297 10651 Glb1 galactosidase, beta 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10861297 10651 Glb1 galactosidase, beta 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:10861297 10651 Glb1 galactosidase, beta 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11578847 10651 Glb1 galactosidase, beta 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9063740 10651 Glb1 galactosidase, beta 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9071485 10651 Glb1 galactosidase, beta 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:9337086 10651 Glb1 galactosidase, beta 1 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:15687347 10651 Glb1 galactosidase, beta 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11578847 10651 Glb1 galactosidase, beta 1 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10861297 10651 Glb1 galactosidase, beta 1 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10861297 10651 Glb1 galactosidase, beta 1 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:11578847 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10805773 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17464988 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:11118286 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:23226398 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:10805773 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10805773 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:10805773 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10805773 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17464988 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17464988 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17464988 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10805773 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17464988 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17464988 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23226398 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:10805773 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10805773 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0004167 abnormal cingulate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:23671099 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17464988 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:17464988 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:17464988 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:17464988 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:23226398 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11118286 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10805773 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:17464988 10652 Gclc glutamate-cysteine ligase, catalytic subunit gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150219 MGI PMID:10805773 10653 Glo1 glyoxalase 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20190314 MGI PMID:28623132 10653 Glo1 glyoxalase 1 gene MP:0001559 hyperglycemia IEA N RGD:5509061 20160428 MGI 10653 Glo1 glyoxalase 1 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20190314 MGI PMID:28623132 10653 Glo1 glyoxalase 1 gene MP:0002727 decreased circulating insulin level IEA N RGD:5509061 20160428 MGI 10653 Glo1 glyoxalase 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20190314 MGI PMID:28623132 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23434938 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23959939 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23434938 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0002694 abnormal pancreas secretion IAGP N RGD:5509061 20141003 MGI PMID:14966573 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14966573 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23434938 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:8898756 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23434938 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:23434938 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23959939 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:14966573 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23959939 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:8898756 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:23434938 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:14966573 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23403053 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23434938 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:8898756 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23434938 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:23434938 10655 Glp1r glucagon-like peptide 1 receptor gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 10656 Glra2 glycine receptor, alpha 2 subunit gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20210128 MGI 10656 Glra2 glycine receptor, alpha 2 subunit gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20210128 MGI 10656 Glra2 glycine receptor, alpha 2 subunit gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 10656 Glra2 glycine receptor, alpha 2 subunit gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17920294 10656 Glra2 glycine receptor, alpha 2 subunit gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:16847326 10656 Glra2 glycine receptor, alpha 2 subunit gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:23954789 10656 Glra2 glycine receptor, alpha 2 subunit gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 10656 Glra2 glycine receptor, alpha 2 subunit gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:23954789 10656 Glra2 glycine receptor, alpha 2 subunit gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 10656 Glra2 glycine receptor, alpha 2 subunit gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 10656 Glra2 glycine receptor, alpha 2 subunit gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:11076688 10657 Glrb glycine receptor, beta subunit gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10651857 10657 Glrb glycine receptor, beta subunit gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0001386 abnormal maternal nurturing IEA N RGD:5509061 20111116 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0001407 short stride length IEA N RGD:5509061 20111116 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:8733750 10657 Glrb glycine receptor, beta subunit gene MP:0001504 abnormal posture IEA N RGD:5509061 20111116 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:10651857 10657 Glrb glycine receptor, beta subunit gene MP:0001522 impaired swimming IEA N RGD:5509061 20111116 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10651857 10657 Glrb glycine receptor, beta subunit gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10651857 10657 Glrb glycine receptor, beta subunit gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20111116 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:10651857 10657 Glrb glycine receptor, beta subunit gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:11076688 10657 Glrb glycine receptor, beta subunit gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0005604 hyperekplexia IAGP N RGD:5509061 20141003 MGI PMID:10651857 10657 Glrb glycine receptor, beta subunit gene MP:0005604 hyperekplexia IAGP N RGD:5509061 20141003 MGI PMID:8733750 10657 Glrb glycine receptor, beta subunit gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0009025 abnormal brain dura mater morphology IAGP N RGD:5509061 20141003 MGI PMID:4323808 10657 Glrb glycine receptor, beta subunit gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 10657 Glrb glycine receptor, beta subunit gene MP:0020422 decreased freezing behavior IEA N RGD:5509061 20231207 MGI 10659 Gls glutaminase gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 10659 Gls glutaminase gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20180503 MGI PMID:28427419 10659 Gls glutaminase gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20141003 MGI PMID:16641247 10659 Gls glutaminase gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20160804 MGI PMID:26778975 10659 Gls glutaminase gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:16641247 10659 Gls glutaminase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16641247 10659 Gls glutaminase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10659 Gls glutaminase gene MP:0030586 impaired behavioral response to amphetamine IAGP N RGD:5509061 20180614 MGI PMID:26778975 10665 Glycam1 glycosylation dependent cell adhesion molecule 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 10665 Glycam1 glycosylation dependent cell adhesion molecule 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 10665 Glycam1 glycosylation dependent cell adhesion molecule 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 10665 Glycam1 glycosylation dependent cell adhesion molecule 1 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20160421 MGI 10669 Gnas GNAS complex locus gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11001929 10669 Gnas GNAS complex locus gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0000088 short mandible IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0000097 short maxilla IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:15765186 10669 Gnas GNAS complex locus gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:15765186 10669 Gnas GNAS complex locus gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:16239968 10669 Gnas GNAS complex locus gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:15273687 10669 Gnas GNAS complex locus gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20170202 MGI PMID:26671181 10669 Gnas GNAS complex locus gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:15811946 10669 Gnas GNAS complex locus gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:15765186 10669 Gnas GNAS complex locus gene MP:0000440 domed cranium IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0000445 short snout IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:15765186 10669 Gnas GNAS complex locus gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:15765186 10669 Gnas GNAS complex locus gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:15273686 10669 Gnas GNAS complex locus gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:21747923 10669 Gnas GNAS complex locus gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0001258 decreased body length IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:19136628 10669 Gnas GNAS complex locus gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:21747923 10669 Gnas GNAS complex locus gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11001929 10669 Gnas GNAS complex locus gene MP:0001262 decreased body weight IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0001265 decreased body size IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15798190 10669 Gnas GNAS complex locus gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15273686 10669 Gnas GNAS complex locus gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:15798190 10669 Gnas GNAS complex locus gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:15273686 10669 Gnas GNAS complex locus gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:11001929 10669 Gnas GNAS complex locus gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:11438605 10669 Gnas GNAS complex locus gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16239968 10669 Gnas GNAS complex locus gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:15273687 10669 Gnas GNAS complex locus gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15765186 10669 Gnas GNAS complex locus gene MP:0001575 cyanosis IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11001929 10669 Gnas GNAS complex locus gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15273686 10669 Gnas GNAS complex locus gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15273686 10669 Gnas GNAS complex locus gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15273687 10669 Gnas GNAS complex locus gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16462745 10669 Gnas GNAS complex locus gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11001929 10669 Gnas GNAS complex locus gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11001929 10669 Gnas GNAS complex locus gene MP:0001954 respiratory distress IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11274197 10669 Gnas GNAS complex locus gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15273686 10669 Gnas GNAS complex locus gene MP:0002083 premature death IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20170202 MGI PMID:26671181 10669 Gnas GNAS complex locus gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:16822937 10669 Gnas GNAS complex locus gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15273687 10669 Gnas GNAS complex locus gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:11001929 10669 Gnas GNAS complex locus gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:11001929 10669 Gnas GNAS complex locus gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:15765186 10669 Gnas GNAS complex locus gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:16822937 10669 Gnas GNAS complex locus gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:15273686 10669 Gnas GNAS complex locus gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:16239968 10669 Gnas GNAS complex locus gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11274197 10669 Gnas GNAS complex locus gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15273686 10669 Gnas GNAS complex locus gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16239968 10669 Gnas GNAS complex locus gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:15273687 10669 Gnas GNAS complex locus gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11274197 10669 Gnas GNAS complex locus gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:15273687 10669 Gnas GNAS complex locus gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20170202 MGI PMID:26671181 10669 Gnas GNAS complex locus gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:15811946 10669 Gnas GNAS complex locus gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16239968 10669 Gnas GNAS complex locus gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:10444578 10669 Gnas GNAS complex locus gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:16822937 10669 Gnas GNAS complex locus gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:15765186 10669 Gnas GNAS complex locus gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0003121 genetic imprinting IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:15811946 10669 Gnas GNAS complex locus gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:15798190 10669 Gnas GNAS complex locus gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:19136628 10669 Gnas GNAS complex locus gene MP:0003353 decreased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:16822937 10669 Gnas GNAS complex locus gene MP:0003416 premature bone ossification IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0003497 insensitivity to parathyroid hormone IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:11438605 10669 Gnas GNAS complex locus gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:15811946 10669 Gnas GNAS complex locus gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:15765186 10669 Gnas GNAS complex locus gene MP:0003705 abnormal hypodermis morphology IAGP N RGD:5509061 20141003 MGI PMID:21747923 10669 Gnas GNAS complex locus gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:11001929 10669 Gnas GNAS complex locus gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:15273686 10669 Gnas GNAS complex locus gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:19136628 10669 Gnas GNAS complex locus gene MP:0003948 abnormal gas homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0003948 abnormal gas homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0003956 abnormal body size IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16822937 10669 Gnas GNAS complex locus gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0004911 absent mandibular condyloid process IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0004913 absent mandibular angle IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11274197 10669 Gnas GNAS complex locus gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16239968 10669 Gnas GNAS complex locus gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:19136628 10669 Gnas GNAS complex locus gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20141003 MGI PMID:15273687 10669 Gnas GNAS complex locus gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:16239968 10669 Gnas GNAS complex locus gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16239968 10669 Gnas GNAS complex locus gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:16822937 10669 Gnas GNAS complex locus gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11274197 10669 Gnas GNAS complex locus gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15273686 10669 Gnas GNAS complex locus gene MP:0005581 abnormal renin activity IAGP N RGD:5509061 20141003 MGI PMID:16822937 10669 Gnas GNAS complex locus gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11438605 10669 Gnas GNAS complex locus gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0006087 increased body mass index IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0008384 absent nasal capsule IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:15273686 10669 Gnas GNAS complex locus gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21455290 10669 Gnas GNAS complex locus gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:16239968 10669 Gnas GNAS complex locus gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15273686 10669 Gnas GNAS complex locus gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0009303 decreased renal fat pad weight IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11274197 10669 Gnas GNAS complex locus gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20170202 MGI PMID:26671181 10669 Gnas GNAS complex locus gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20170202 MGI PMID:26671181 10669 Gnas GNAS complex locus gene MP:0009673 increased birth weight IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0009702 increased birth body size IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15273687 10669 Gnas GNAS complex locus gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0009892 palate bone hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0009908 protruding tongue IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0009917 abnormal hyoid bone body morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16239968 10669 Gnas GNAS complex locus gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20160714 MGI PMID:21220306 10669 Gnas GNAS complex locus gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:16239968 10669 Gnas GNAS complex locus gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11001929 10669 Gnas GNAS complex locus gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15273686 10669 Gnas GNAS complex locus gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15883378 10669 Gnas GNAS complex locus gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19136628 10669 Gnas GNAS complex locus gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15765186 10669 Gnas GNAS complex locus gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22253771 10669 Gnas GNAS complex locus gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11001929 10669 Gnas GNAS complex locus gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11001929 10669 Gnas GNAS complex locus gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0011478 abnormal urine catecholamine level IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0011563 increased urine prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:16822937 10669 Gnas GNAS complex locus gene MP:0011612 increased circulating ghrelin level IAGP N RGD:5509061 20141003 MGI PMID:22253771 10669 Gnas GNAS complex locus gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:22215617 10669 Gnas GNAS complex locus gene MP:0012336 decreased vitamin D level IAGP N RGD:5509061 20170202 MGI PMID:26671181 10669 Gnas GNAS complex locus gene MP:0013585 thymus cortex atrophy IAGP N RGD:5509061 20150319 MGI PMID:9671744 10669 Gnas GNAS complex locus gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0014167 ectopic bone IAGP N RGD:5509061 20160407 MGI PMID:21747923 10669 Gnas GNAS complex locus gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20171228 MGI PMID:20374964 10669 Gnas GNAS complex locus gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:11274197 10669 Gnas GNAS complex locus gene MP:0030072 round face IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0030200 abnormal nasal septum cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0030367 premature metopic suture closure IAGP N RGD:5509061 20221110 MGI PMID:26859889 10669 Gnas GNAS complex locus gene MP:0030768 increased urine dopamine level IAGP N RGD:5509061 20180927 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0030772 increased urine noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0030773 decreased urine noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:10712433 10669 Gnas GNAS complex locus gene MP:0031414 decreased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:20374964 10671 Gnmt glycine N-methyltransferase gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17937387 10671 Gnmt glycine N-methyltransferase gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17937387 10671 Gnmt glycine N-methyltransferase gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17937387 10671 Gnmt glycine N-methyltransferase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17937387 10671 Gnmt glycine N-methyltransferase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:17937387 10671 Gnmt glycine N-methyltransferase gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:17937387 10671 Gnmt glycine N-methyltransferase gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:17937387 10671 Gnmt glycine N-methyltransferase gene MP:0002047 increased hepatic hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:19035462 10671 Gnmt glycine N-methyltransferase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160310 MGI PMID:19035462 10671 Gnmt glycine N-methyltransferase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17937387 10671 Gnmt glycine N-methyltransferase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19035462 10671 Gnmt glycine N-methyltransferase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17937387 10671 Gnmt glycine N-methyltransferase gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:17937387 10671 Gnmt glycine N-methyltransferase gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19035462 10671 Gnmt glycine N-methyltransferase gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17937387 10671 Gnmt glycine N-methyltransferase gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17937387 10671 Gnmt glycine N-methyltransferase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:16779654 10671 Gnmt glycine N-methyltransferase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17937387 10671 Gnmt glycine N-methyltransferase gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20200910 MGI PMID:17937387 10671 Gnmt glycine N-methyltransferase gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20160310 MGI PMID:17937387 10671 Gnmt glycine N-methyltransferase gene MP:0030644 increased circulating methionine level IAGP N RGD:5509061 20180920 MGI PMID:17937387 10675 Got1 glutamic-oxaloacetic transaminase 1, soluble gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 10675 Got1 glutamic-oxaloacetic transaminase 1, soluble gene MP:0002607 decreased basophil cell number IEA N RGD:5509061 20211021 MGI 10675 Got1 glutamic-oxaloacetic transaminase 1, soluble gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210520 MGI 10675 Got1 glutamic-oxaloacetic transaminase 1, soluble gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 10675 Got1 glutamic-oxaloacetic transaminase 1, soluble gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20221215 MGI 10675 Got1 glutamic-oxaloacetic transaminase 1, soluble gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10675 Got1 glutamic-oxaloacetic transaminase 1, soluble gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 10676 Gp5 glycoprotein 5 platelet gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10590056 10676 Gp5 glycoprotein 5 platelet gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:10557321 10677 Gpc3 glypican 3 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:10964473 10677 Gpc3 glypican 3 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:10964473 10677 Gpc3 glypican 3 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:19733558 10677 Gpc3 glypican 3 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:10964473 10677 Gpc3 glypican 3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0001123 dilated uterus IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:10964473 10677 Gpc3 glypican 3 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0001699 increased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11431694 10677 Gpc3 glypican 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0001867 rhinitis IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20150924 MGI PMID:23327927 10677 Gpc3 glypican 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0002707 abnormal kidney weight IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:10964473 10677 Gpc3 glypican 3 gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:11180950 10677 Gpc3 glypican 3 gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:19733558 10677 Gpc3 glypican 3 gene MP:0003315 abnormal perineum morphology IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:10964473 10677 Gpc3 glypican 3 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:10964473 10677 Gpc3 glypican 3 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:11180950 10677 Gpc3 glypican 3 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:11431694 10677 Gpc3 glypican 3 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0003956 abnormal body size IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:10964473 10677 Gpc3 glypican 3 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:11180950 10677 Gpc3 glypican 3 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20150924 MGI PMID:23327927 10677 Gpc3 glypican 3 gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15936336 10677 Gpc3 glypican 3 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:10964473 10677 Gpc3 glypican 3 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:15936336 10677 Gpc3 glypican 3 gene MP:0009728 abnormal calcaneum morphology IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0010146 umbilical hernia IAGP N RGD:5509061 20141003 MGI PMID:10964473 10677 Gpc3 glypican 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19733558 10677 Gpc3 glypican 3 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19733558 10677 Gpc3 glypican 3 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19733558 10677 Gpc3 glypican 3 gene MP:0010419 inlet ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19733558 10677 Gpc3 glypican 3 gene MP:0010476 coronary fistula IAGP N RGD:5509061 20141003 MGI PMID:19733558 10677 Gpc3 glypican 3 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19733558 10677 Gpc3 glypican 3 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:19733558 10677 Gpc3 glypican 3 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20150924 MGI PMID:23327927 10677 Gpc3 glypican 3 gene MP:0010981 abnormal branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10402475 10677 Gpc3 glypican 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11431694 10677 Gpc3 glypican 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10964473 10677 Gpc3 glypican 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20141003 MGI PMID:10964473 10677 Gpc3 glypican 3 gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0011308 kidney corticomedullary cyst IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0011520 increased placental labyrinth size IAGP N RGD:5509061 20141003 MGI PMID:11846487 10677 Gpc3 glypican 3 gene MP:0014347 increased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:11846487 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12644183 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:1582174 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8408535 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2344351 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8417789 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2381920 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2381920 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8408535 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:162283 10680 Gpi1 glucose-6-phosphate isomerase 1 gene MP:0031084 decreased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:8417789 10681 Gpx1 glutathione peroxidase 1 gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20180719 MGI PMID:14732290 10681 Gpx1 glutathione peroxidase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:14732290 10681 Gpx1 glutathione peroxidase 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20180719 MGI PMID:14732290 10681 Gpx1 glutathione peroxidase 1 gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20180719 MGI PMID:11518697 10681 Gpx1 glutathione peroxidase 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20180719 MGI 10681 Gpx1 glutathione peroxidase 1 gene MP:0001147 small testis IEA N RGD:5509061 20180719 MGI 10681 Gpx1 glutathione peroxidase 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 10681 Gpx1 glutathione peroxidase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180719 MGI PMID:10754271 10681 Gpx1 glutathione peroxidase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180719 MGI PMID:11518697 10681 Gpx1 glutathione peroxidase 1 gene MP:0001304 cataract IAGP N RGD:5509061 20180719 MGI PMID:18760274 10681 Gpx1 glutathione peroxidase 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180719 MGI PMID:24075852 10681 Gpx1 glutathione peroxidase 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20180719 MGI PMID:10754271 10681 Gpx1 glutathione peroxidase 1 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20180719 MGI PMID:11518697 10681 Gpx1 glutathione peroxidase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180719 MGI PMID:11518697 10681 Gpx1 glutathione peroxidase 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20180719 MGI PMID:12429206 10681 Gpx1 glutathione peroxidase 1 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20180719 MGI PMID:11518697 10681 Gpx1 glutathione peroxidase 1 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20180719 MGI PMID:24075852 10681 Gpx1 glutathione peroxidase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:11518697 10681 Gpx1 glutathione peroxidase 1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20180719 MGI 10681 Gpx1 glutathione peroxidase 1 gene MP:0002816 colitis IAGP N RGD:5509061 20180719 MGI PMID:11518697 10681 Gpx1 glutathione peroxidase 1 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20180719 MGI PMID:11545230 10681 Gpx1 glutathione peroxidase 1 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20180719 MGI PMID:11579147 10681 Gpx1 glutathione peroxidase 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20180719 MGI PMID:14732290 10681 Gpx1 glutathione peroxidase 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20180719 MGI PMID:11579147 10681 Gpx1 glutathione peroxidase 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20180719 MGI PMID:12429206 10681 Gpx1 glutathione peroxidase 1 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20180719 MGI PMID:10915653 10681 Gpx1 glutathione peroxidase 1 gene MP:0003288 intestinal edema IAGP N RGD:5509061 20180719 MGI PMID:11518697 10681 Gpx1 glutathione peroxidase 1 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20180719 MGI PMID:11518697 10681 Gpx1 glutathione peroxidase 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20180719 MGI PMID:11579147 10681 Gpx1 glutathione peroxidase 1 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20180719 MGI PMID:11545230 10681 Gpx1 glutathione peroxidase 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20180719 MGI PMID:11545230 10681 Gpx1 glutathione peroxidase 1 gene MP:0004597 increased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20180719 MGI PMID:11545230 10681 Gpx1 glutathione peroxidase 1 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20180719 MGI 10681 Gpx1 glutathione peroxidase 1 gene MP:0005035 perianal ulcer IAGP N RGD:5509061 20180719 MGI PMID:11518697 10681 Gpx1 glutathione peroxidase 1 gene MP:0005036 diarrhea IAGP N RGD:5509061 20180719 MGI PMID:11518697 10681 Gpx1 glutathione peroxidase 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20180719 MGI PMID:11518697 10681 Gpx1 glutathione peroxidase 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20180719 MGI PMID:12429206 10681 Gpx1 glutathione peroxidase 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20180719 MGI PMID:11518697 10681 Gpx1 glutathione peroxidase 1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20180719 MGI PMID:9195979 10681 Gpx1 glutathione peroxidase 1 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20180719 MGI PMID:11518697 10681 Gpx1 glutathione peroxidase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180719 MGI PMID:11518697 10681 Gpx1 glutathione peroxidase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180719 MGI PMID:8759521 10681 Gpx1 glutathione peroxidase 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180719 MGI PMID:10754271 10681 Gpx1 glutathione peroxidase 1 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20180719 MGI PMID:11579147 10681 Gpx1 glutathione peroxidase 1 gene MP:0006080 brain ischemia IAGP N RGD:5509061 20180719 MGI PMID:11579147 10681 Gpx1 glutathione peroxidase 1 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20180719 MGI PMID:14732290 10681 Gpx1 glutathione peroxidase 1 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20180719 MGI PMID:14732290 10681 Gpx1 glutathione peroxidase 1 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20180719 MGI PMID:9712879 10681 Gpx1 glutathione peroxidase 1 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180719 MGI PMID:24075852 10681 Gpx1 glutathione peroxidase 1 gene MP:0011592 abnormal catalase activity IAGP N RGD:5509061 20180719 MGI PMID:8759521 10681 Gpx1 glutathione peroxidase 1 gene MP:0011603 decreased glutathione peroxidase activity IAGP N RGD:5509061 20180719 MGI PMID:20015939 10681 Gpx1 glutathione peroxidase 1 gene MP:0011603 decreased glutathione peroxidase activity IAGP N RGD:5509061 20180719 MGI PMID:8759521 10681 Gpx1 glutathione peroxidase 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20180719 MGI PMID:11545230 10681 Gpx1 glutathione peroxidase 1 gene MP:0013481 abnormal ileum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20180719 MGI PMID:10915653 10681 Gpx1 glutathione peroxidase 1 gene MP:0013483 abnormal jejunum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20180719 MGI PMID:10915653 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19726645 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0001901 absence of NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19726645 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19726645 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19142228 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:19142228 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19778510 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:19778510 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0002980 abnormal postural reflex IAGP N RGD:5509061 20141003 MGI PMID:19142228 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19142228 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:19142228 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19726645 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19778510 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200514 MGI 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:19726645 10683 Grik4 glutamate receptor, ionotropic, kainate 4 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0000774 decreased brain size IEA N RGD:5509061 20210520 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0001258 decreased body length IEA N RGD:5509061 20210520 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0001304 cataract IEA N RGD:5509061 20210826 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0001488 increased startle reflex IEA N RGD:5509061 20111116 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210520 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12533602 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0002906 increased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20111116 MGI 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12533602 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19778510 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:19778510 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19778510 10684 Grik5 glutamate receptor, ionotropic, kainate 5 (gamma 2) gene MP:0011274 short excitatory postsynaptic current decay time IAGP N RGD:5509061 20141003 MGI PMID:12533602 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10963597 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0000860 abnormal primary somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12498788 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0000862 absent barrels in primary somatosensory cortex IAGP N RGD:5509061 20141003 MGI PMID:10963597 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0000862 absent barrels in primary somatosensory cortex IAGP N RGD:5509061 20141003 MGI PMID:12498788 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12657691 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:8060614 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8060614 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:8060614 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10481908 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10818139 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10963597 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:10481908 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:19776282 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:19915563 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:20345915 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20181220 MGI PMID:22726567 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:10481908 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:24244696 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19915563 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:10481908 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20181220 MGI PMID:22726567 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:10818139 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:8313466 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12657691 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20345915 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10818139 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:10481908 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:20345915 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20141003 MGI PMID:19915563 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22419158 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001435 absent suckling reflex IAGP N RGD:5509061 20141003 MGI PMID:10818139 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:8313466 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:8713451 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20181220 MGI PMID:22726567 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:19915563 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:10700255 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001460 abnormal olfactory discrimination memory IAGP N RGD:5509061 20141003 MGI PMID:10700255 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10818139 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11073458 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12040087 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:8980238 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:9054942 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:10700255 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11073458 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15003177 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10818139 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12040087 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17015831 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18701073 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19776282 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:8980238 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:10818139 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15265649 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20181220 MGI PMID:22726567 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001513 limb grasping IAGP N RGD:5509061 20181220 MGI PMID:22726567 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12657691 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8060614 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8313466 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8713451 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:10963597 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10818139 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:17015831 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:17556551 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001901 absence of NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001901 absence of NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:11073458 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001901 absence of NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15003177 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001901 absence of NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16099814 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001901 absence of NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:8060614 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001901 absence of NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:8313466 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001901 absence of NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:8980238 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23277569 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001909 reduced NMDA receptor mediated synaptic activity in barrel cortex IAGP N RGD:5509061 20141003 MGI PMID:10963597 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10481908 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12657691 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:8313466 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:11073458 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:16101757 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:10481908 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:22419158 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:23277569 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17313573 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12657691 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19142228 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19915563 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:10481908 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:19915563 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:19776282 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:19915563 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002802 abnormal discrimination learning IAGP N RGD:5509061 20141003 MGI PMID:17556551 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:17015831 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:16101757 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:24244696 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18701074 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:18701074 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:19776282 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:8060614 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:8713451 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:10818139 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12040087 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17015831 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18701074 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23277569 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:24244696 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:19142228 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17015831 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18701073 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:8980238 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002969 impaired social transmission of food preference IAGP N RGD:5509061 20141003 MGI PMID:10700255 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0002980 abnormal postural reflex IAGP N RGD:5509061 20141003 MGI PMID:19142228 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20160804 MGI 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:12040087 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:24244696 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:24244696 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:10818139 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:15265649 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19142228 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0004000 impaired passive avoidance behavior IEA N RGD:5509061 20111116 MGI 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20181220 MGI PMID:22726567 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18701073 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19776282 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23277569 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:20345915 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:19142228 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:12657691 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:8313466 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0005572 abnormal pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0006335 abnormal hearing electrophysiology IAGP N RGD:5509061 20181220 MGI PMID:22726567 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:8713451 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:17313573 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:19915563 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20181220 MGI PMID:22726567 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17015831 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20345915 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:15265649 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:19776282 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:19915563 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20181220 MGI PMID:22726567 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0009326 absent maternal crouching IAGP N RGD:5509061 20220519 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0009327 abnormal maternal grooming IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:8060614 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:8713451 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:18701073 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20345915 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:18701073 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:18701074 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19776282 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10818139 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24244696 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20345915 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12657691 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8313466 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8713451 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8060614 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20345915 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:23277569 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0014274 decreased respiration IAGP N RGD:5509061 20230810 MGI PMID:10729336 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0014373 increased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:18701073 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0014375 increased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:18701073 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0020157 abnormal behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:24244696 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20181220 MGI PMID:22726567 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0021117 abnormal huddling behavior IAGP N RGD:5509061 20220519 MGI PMID:10481908 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:10481908 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:19915563 10685 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1) gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22726567 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23201971 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20161229 MGI PMID:27317637 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001401 jumpy IAGP N RGD:5509061 20141003 MGI PMID:7816096 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23201971 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9458051 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20161229 MGI PMID:27317637 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:7816096 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:23201971 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:7816096 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:9458051 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:11488959 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001500 decreased kindling response IAGP N RGD:5509061 20141003 MGI PMID:9458051 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:15317856 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:8987814 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19834457 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:7816096 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:21725314 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:8987814 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19834457 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21725314 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:8987814 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0003177 allodynia IAGP N RGD:5509061 20141003 MGI PMID:21725314 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:19834457 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21725314 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:8987814 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20161229 MGI PMID:27317637 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0008532 decreased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21725314 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23201971 10686 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1) gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:9458051 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0000861 disorganized barrel cortex IAGP N RGD:5509061 20141003 MGI PMID:8789948 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22153375 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:22153375 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:22153375 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23201971 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23201971 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001435 absent suckling reflex IAGP N RGD:5509061 20141003 MGI PMID:8789948 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:22153375 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16710293 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:20357110 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001468 abnormal temporal memory IAGP N RGD:5509061 20141003 MGI PMID:22234183 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19726645 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:20357110 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22234183 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:23201971 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:20357110 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:11488959 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:20357110 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:9768843 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:20357110 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:8789948 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:16710293 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001901 absence of NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19726645 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0001901 absence of NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:8789948 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:20357110 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:20357110 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22153375 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:9768843 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:22153375 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:20357110 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002802 abnormal discrimination learning IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23201971 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22153375 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16870468 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22153375 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:9458051 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20357110 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:20357110 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:9768843 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:23201971 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0003063 increased coping response IAGP N RGD:5509061 20230413 MGI PMID:34433031 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:16710293 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20230413 MGI PMID:34433031 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22153375 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20230413 MGI PMID:34433031 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19726645 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20357110 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:11488959 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:19726645 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:8789948 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9768843 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8789948 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9458051 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19081379 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210805 MGI 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:20357110 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0011274 short excitatory postsynaptic current decay time IAGP N RGD:5509061 20240418 MGI PMID:20357110 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0020507 increased dendritic spine density IAGP N RGD:5509061 20230413 MGI PMID:34433031 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20211014 MGI PMID:20357110 10687 Grin2b glutamate receptor, ionotropic, NMDA2B (epsilon 2) gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22153375 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:15519237 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:15519237 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15519237 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9458051 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:15317856 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:8987814 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:9458051 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15317856 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17276696 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:8756432 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:8987814 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:8756432 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:8987814 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:8987814 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:15519237 10688 Grin2c glutamate receptor, ionotropic, NMDA2C (epsilon 3) gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:9458051 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:10471508 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:10471508 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20519123 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:10471508 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:12949501 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:18697839 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:18697839 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0000643 absent adrenal medulla IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0000645 absent adrenergic chromaffin cells IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0000646 enlarged adrenocortical cells IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12165507 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:14578211 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:12165507 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:14578211 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:12165507 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:14578211 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:20519123 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:10471508 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10471508 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17504935 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22232675 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10471508 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10471508 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15623560 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001742 absent circulating adrenaline IAGP N RGD:5509061 20141003 MGI PMID:10357937 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:14578211 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15623560 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:17683525 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:18697839 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:22232675 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:9604929 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:22232675 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001753 hypersecretion of corticotropin-releasing hormone IAGP N RGD:5509061 20141003 MGI PMID:10471508 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:22653054 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22653054 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:15623560 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:12495930 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20141003 MGI PMID:10471508 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12133953 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:14578211 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19234455 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14578211 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002324 abnormal alveolocapillary membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:14578211 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:15623560 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002664 decreased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:10471508 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002664 decreased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:19017639 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:19017639 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:18697839 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:19017639 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:19017639 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0003075 abnormal response to CNS ischemic injury IAGP N RGD:5509061 20161103 MGI PMID:23637179 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0003115 abnormal respiratory system development IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0003367 increased circulating glucocorticoid level IAGP N RGD:5509061 20141003 MGI PMID:10471508 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0003711 pathological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:19017639 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0004202 pulmonary hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:14578211 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0004733 abnormal thoracic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:14578211 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:18523311 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19017639 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:20519123 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19017639 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22653054 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0005129 increased adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:10471508 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0005167 abnormal blood-brain barrier function IAGP N RGD:5509061 20141003 MGI PMID:18523311 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:18697839 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0005582 increased renin activity IAGP N RGD:5509061 20141003 MGI PMID:18697839 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:14578211 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20141003 MGI PMID:22232675 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0005664 decreased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:10357937 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18697839 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:15471946 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0006375 increased circulating angiotensinogen level IAGP N RGD:5509061 20141003 MGI PMID:18697839 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16424199 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18523311 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19017639 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22653054 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19017639 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22653054 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22653054 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20161103 MGI PMID:23637179 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:20519123 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008292 enlarged adrenocortical cell nuclei IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008293 abnormal adrenal gland zona glomerulosa morphology IAGP N RGD:5509061 20141003 MGI PMID:18697839 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008294 abnormal adrenal gland zona fasciculata morphology IAGP N RGD:5509061 20141003 MGI PMID:18697839 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008295 abnormal adrenal gland zona reticularis morphology IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008302 thin adrenal cortex IAGP N RGD:5509061 20141003 MGI PMID:19017639 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:20519123 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008504 abnormal adrenal chromaffin cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10357937 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008504 abnormal adrenal chromaffin cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20161103 MGI PMID:23637179 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008704 abnormal interleukin-6 secretion IAGP N RGD:5509061 20161103 MGI PMID:23637179 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12949501 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:12949501 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:12949501 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:12949501 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:10357937 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:12495930 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19017639 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18523311 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:10580006 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0009258 abnormal thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12165507 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18697839 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20141003 MGI PMID:12949501 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:15471946 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22653054 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:19234455 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12949501 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0010119 abnormal bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20519123 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:14578211 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0010816 decreased type I pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:14578211 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20220915 MGI PMID:20519123 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0011031 abnormal branching involved in terminal bronchiole morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18697839 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10357937 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12165507 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12495930 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12495930 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14578211 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10357937 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22232675 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20141003 MGI PMID:24082121 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0012441 abnormal monocyte cell number IAGP N RGD:5509061 20161103 MGI PMID:23637179 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20220915 MGI PMID:20519123 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0014286 increased adrenal gland zona fasciculata size IAGP N RGD:5509061 20230907 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0014287 decreased adrenal gland zona fasciculata size IAGP N RGD:5509061 20230907 MGI PMID:19017639 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0030762 decreased adrenaline level IAGP N RGD:5509061 20180927 MGI PMID:7628695 10691 Nr3c1 nuclear receptor subfamily 3, group C, member 1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:24082121 10693 Gspt1 G1 to S phase transition 1 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241010 MGI 10693 Gspt1 G1 to S phase transition 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 10693 Gspt1 G1 to S phase transition 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 10694 Gss glutathione synthetase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21802407 10697 Gstm1 glutathione S-transferase, mu 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20178820 10697 Gstm1 glutathione S-transferase, mu 1 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:20178820 10697 Gstm1 glutathione S-transferase, mu 1 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:20178820 10697 Gstm1 glutathione S-transferase, mu 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20178820 10697 Gstm1 glutathione S-transferase, mu 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20178820 10697 Gstm1 glutathione S-transferase, mu 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:16760226 10697 Gstm1 glutathione S-transferase, mu 1 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20178820 10697 Gstm1 glutathione S-transferase, mu 1 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:20178820 10697 Gstm1 glutathione S-transferase, mu 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:20178820 10700 Gstt1 glutathione S-transferase, theta 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 10700 Gstt1 glutathione S-transferase, theta 1 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20160804 MGI 10700 Gstt1 glutathione S-transferase, theta 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:17827337 10706 Hdc histidine decarboxylase gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12960041 10706 Hdc histidine decarboxylase gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12960041 10706 Hdc histidine decarboxylase gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:11478947 10706 Hdc histidine decarboxylase gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11478947 10706 Hdc histidine decarboxylase gene MP:0000361 decreased mast cell protease storage IAGP N RGD:5509061 20141003 MGI PMID:11478947 10706 Hdc histidine decarboxylase gene MP:0000362 decreased mast cell histamine storage IAGP N RGD:5509061 20141003 MGI PMID:11478947 10706 Hdc histidine decarboxylase gene MP:0000836 abnormal substantia nigra morphology IAGP N RGD:5509061 20151210 MGI PMID:24411733 10706 Hdc histidine decarboxylase gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12960041 10706 Hdc histidine decarboxylase gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16310870 10706 Hdc histidine decarboxylase gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16412995 10706 Hdc histidine decarboxylase gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:16310870 10706 Hdc histidine decarboxylase gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16310870 10706 Hdc histidine decarboxylase gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20151210 MGI PMID:24411733 10706 Hdc histidine decarboxylase gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:16212954 10706 Hdc histidine decarboxylase gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:16310870 10706 Hdc histidine decarboxylase gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:16412995 10706 Hdc histidine decarboxylase gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12960041 10706 Hdc histidine decarboxylase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12960041 10706 Hdc histidine decarboxylase gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:16212954 10706 Hdc histidine decarboxylase gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:16412995 10706 Hdc histidine decarboxylase gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22993424 10706 Hdc histidine decarboxylase gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:22993424 10706 Hdc histidine decarboxylase gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20151210 MGI PMID:24411733 10706 Hdc histidine decarboxylase gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22993424 10706 Hdc histidine decarboxylase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12960041 10706 Hdc histidine decarboxylase gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:12960041 10706 Hdc histidine decarboxylase gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:12960041 10706 Hdc histidine decarboxylase gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12960041 10706 Hdc histidine decarboxylase gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:16212954 10706 Hdc histidine decarboxylase gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:12960041 10706 Hdc histidine decarboxylase gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20151210 MGI PMID:24411733 10706 Hdc histidine decarboxylase gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12960041 10706 Hdc histidine decarboxylase gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12960041 10706 Hdc histidine decarboxylase gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20141003 MGI PMID:22993424 10706 Hdc histidine decarboxylase gene MP:0013894 abnormal behavioral response to amphetamine IAGP N RGD:5509061 20151210 MGI PMID:24411733 10707 Hexa hexosaminidase A gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9184660 10707 Hexa hexosaminidase A gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9184660 10707 Hexa hexosaminidase A gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9184660 10707 Hexa hexosaminidase A gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9184660 10707 Hexa hexosaminidase A gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8747922 10707 Hexa hexosaminidase A gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:9184660 10707 Hexa hexosaminidase A gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:14972652 10707 Hexa hexosaminidase A gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9184660 10707 Hexa hexosaminidase A gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:14972652 10707 Hexa hexosaminidase A gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:14972652 10707 Hexa hexosaminidase A gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:14972652 10707 Hexa hexosaminidase A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9645704 10707 Hexa hexosaminidase A gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:14972652 10707 Hexa hexosaminidase A gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:9184660 10707 Hexa hexosaminidase A gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:7937929 10707 Hexa hexosaminidase A gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:9645704 10707 Hexa hexosaminidase A gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:14972652 10707 Hexa hexosaminidase A gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:14972652 10707 Hexa hexosaminidase A gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:7937929 10707 Hexa hexosaminidase A gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8747922 10707 Hexa hexosaminidase A gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:8789434 10707 Hexa hexosaminidase A gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:9184660 10707 Hexa hexosaminidase A gene MP:0003807 camptodactyly IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0004676 wide ribs IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0011473 increased urine glycosaminoglycan level IAGP N RGD:5509061 20141003 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0030189 broad snout IAGP N RGD:5509061 20171019 MGI PMID:8896570 10707 Hexa hexosaminidase A gene MP:0030262 frontal bossing IAGP N RGD:5509061 20171026 MGI PMID:8896570 10708 Hgf hepatocyte growth factor gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20200813 MGI PMID:32152201 10708 Hgf hepatocyte growth factor gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20200813 MGI PMID:32152201 10708 Hgf hepatocyte growth factor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:7854452 10708 Hgf hepatocyte growth factor gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7854452 10708 Hgf hepatocyte growth factor gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:7854452 10708 Hgf hepatocyte growth factor gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:7854453 10708 Hgf hepatocyte growth factor gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:7854452 10708 Hgf hepatocyte growth factor gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7854452 10708 Hgf hepatocyte growth factor gene MP:0000608 dissociated hepatocytes IAGP N RGD:5509061 20141003 MGI PMID:7854452 10708 Hgf hepatocyte growth factor gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7854452 10708 Hgf hepatocyte growth factor gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:7854452 10708 Hgf hepatocyte growth factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7854453 10708 Hgf hepatocyte growth factor gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:7854452 10708 Hgf hepatocyte growth factor gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:7854452 10708 Hgf hepatocyte growth factor gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:7854453 10708 Hgf hepatocyte growth factor gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7854452 10708 Hgf hepatocyte growth factor gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15383179 10708 Hgf hepatocyte growth factor gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:7854453 10708 Hgf hepatocyte growth factor gene MP:0004300 abnormal organ of Corti supporting cell morphology IAGP N RGD:5509061 20200813 MGI PMID:32152201 10708 Hgf hepatocyte growth factor gene MP:0004364 thin stria vascularis IAGP N RGD:5509061 20200813 MGI PMID:32152201 10708 Hgf hepatocyte growth factor gene MP:0004367 abnormal strial intermediate cell morphology IAGP N RGD:5509061 20200813 MGI PMID:32152201 10708 Hgf hepatocyte growth factor gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20200813 MGI PMID:32152201 10708 Hgf hepatocyte growth factor gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20200813 MGI PMID:32152201 10708 Hgf hepatocyte growth factor gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20200813 MGI PMID:32152201 10708 Hgf hepatocyte growth factor gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20200813 MGI PMID:32152201 10708 Hgf hepatocyte growth factor gene MP:0004864 spiral ligament degeneration IAGP N RGD:5509061 20200813 MGI PMID:32152201 10708 Hgf hepatocyte growth factor gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:15383179 10708 Hgf hepatocyte growth factor gene MP:0006325 impaired hearing IAGP N RGD:5509061 20200813 MGI PMID:32152201 10708 Hgf hepatocyte growth factor gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:7854453 10708 Hgf hepatocyte growth factor gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:7854452 10708 Hgf hepatocyte growth factor gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17923692 10708 Hgf hepatocyte growth factor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7854452 10708 Hgf hepatocyte growth factor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7854453 10708 Hgf hepatocyte growth factor gene MP:0011527 disorganized placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:7854452 10710 Hk1 hexokinase 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0002814 hyperchromasia IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:11783948 10710 Hk1 hexokinase 1 gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20141003 MGI PMID:11783948 10711 Hmgb1 high mobility group box 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:10391216 10711 Hmgb1 high mobility group box 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:10391216 10711 Hmgb1 high mobility group box 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:10391216 10711 Hmgb1 high mobility group box 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10391216 10711 Hmgb1 high mobility group box 1 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:24302768 10711 Hmgb1 high mobility group box 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10391216 10711 Hmgb1 high mobility group box 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:24302768 10711 Hmgb1 high mobility group box 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:24302768 10711 Hmgb1 high mobility group box 1 gene MP:0002715 decreased glycogen catabolism rate IAGP N RGD:5509061 20141003 MGI PMID:10391216 10711 Hmgb1 high mobility group box 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:24302768 10711 Hmgb1 high mobility group box 1 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:15649368 10711 Hmgb1 high mobility group box 1 gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20160204 MGI PMID:24361123 10711 Hmgb1 high mobility group box 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10391216 10711 Hmgb1 high mobility group box 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:10391216 10711 Hmgb1 high mobility group box 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20160204 MGI PMID:24361123 10711 Hmgb1 high mobility group box 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20160204 MGI PMID:24361123 10711 Hmgb1 high mobility group box 1 gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:24302768 10711 Hmgb1 high mobility group box 1 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:24302768 10711 Hmgb1 high mobility group box 1 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:24302768 10711 Hmgb1 high mobility group box 1 gene MP:0008684 increased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:24302768 10711 Hmgb1 high mobility group box 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:24302768 10711 Hmgb1 high mobility group box 1 gene MP:0008806 increased circulating amylase level IAGP N RGD:5509061 20160204 MGI PMID:24361123 10711 Hmgb1 high mobility group box 1 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:24302768 10711 Hmgb1 high mobility group box 1 gene MP:0009148 pancreas necrosis IAGP N RGD:5509061 20160204 MGI PMID:24361123 10711 Hmgb1 high mobility group box 1 gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24302768 10711 Hmgb1 high mobility group box 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10391216 10711 Hmgb1 high mobility group box 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24302768 10711 Hmgb1 high mobility group box 1 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20160204 MGI PMID:24361123 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20220901 MGI PMID:35421611 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0000603 pale liver IAGP N RGD:5509061 20220901 MGI PMID:35421611 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220901 MGI PMID:35421611 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20220901 MGI PMID:35421611 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20220901 MGI PMID:35421611 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0003457 abnormal circulating ketone body level IAGP N RGD:5509061 20220901 MGI PMID:35421611 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20220901 MGI PMID:35421611 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20220901 MGI PMID:35421611 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20220901 MGI PMID:35421611 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20200528 MGI PMID:31910233 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20220901 MGI PMID:35421611 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20220901 MGI PMID:35421611 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20220901 MGI PMID:35421611 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20220901 MGI PMID:35421611 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20220901 MGI PMID:35421611 10713 Hmgcs2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20220901 MGI PMID:35421611 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20200402 MGI 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20151203 MGI PMID:25750434 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:14534534 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20151203 MGI PMID:25750434 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20151203 MGI PMID:25750434 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14534534 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20151203 MGI PMID:25750434 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0002764 short tibia IEA N RGD:5509061 20190502 MGI 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210520 MGI 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20151203 MGI PMID:25750434 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20151203 MGI PMID:25750434 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20151203 MGI PMID:25750434 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20151203 MGI PMID:25750434 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20151203 MGI PMID:25750434 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 10714 Hmmr hyaluronan mediated motility receptor (RHAMM) gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:25750434 10717 Hmox1 heme oxygenase 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:10207174 10717 Hmox1 heme oxygenase 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20201022 MGI 10717 Hmox1 heme oxygenase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 10717 Hmox1 heme oxygenase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0001443 poor grooming IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11273999 10717 Hmox1 heme oxygenase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20210610 MGI PMID:31571584 10717 Hmox1 heme oxygenase 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20210610 MGI PMID:31571584 10717 Hmox1 heme oxygenase 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 10717 Hmox1 heme oxygenase 1 gene MP:0001785 edema IEA N RGD:5509061 20230601 MGI 10717 Hmox1 heme oxygenase 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 10717 Hmox1 heme oxygenase 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11385506 10717 Hmox1 heme oxygenase 1 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:10207174 10717 Hmox1 heme oxygenase 1 gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19706490 10717 Hmox1 heme oxygenase 1 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11273999 10717 Hmox1 heme oxygenase 1 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:11273999 10717 Hmox1 heme oxygenase 1 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20210610 MGI PMID:31571584 10717 Hmox1 heme oxygenase 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10207174 10717 Hmox1 heme oxygenase 1 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10207174 10717 Hmox1 heme oxygenase 1 gene MP:0003326 liver failure IAGP N RGD:5509061 20141003 MGI PMID:19706490 10717 Hmox1 heme oxygenase 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:10807584 10717 Hmox1 heme oxygenase 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:10207174 10717 Hmox1 heme oxygenase 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20220519 MGI 10717 Hmox1 heme oxygenase 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:24630724 10717 Hmox1 heme oxygenase 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20210610 MGI PMID:31571584 10717 Hmox1 heme oxygenase 1 gene MP:0003913 increased heart right ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:10207174 10717 Hmox1 heme oxygenase 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 10717 Hmox1 heme oxygenase 1 gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10807584 10717 Hmox1 heme oxygenase 1 gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:10807584 10717 Hmox1 heme oxygenase 1 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20210826 MGI 10717 Hmox1 heme oxygenase 1 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:19706490 10717 Hmox1 heme oxygenase 1 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:10207174 10717 Hmox1 heme oxygenase 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:10807584 10717 Hmox1 heme oxygenase 1 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11385506 10717 Hmox1 heme oxygenase 1 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:10207174 10717 Hmox1 heme oxygenase 1 gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:11273999 10717 Hmox1 heme oxygenase 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0010750 increased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19706490 10717 Hmox1 heme oxygenase 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20150917 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10207174 10717 Hmox1 heme oxygenase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10207174 10717 Hmox1 heme oxygenase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11273999 10717 Hmox1 heme oxygenase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 10717 Hmox1 heme oxygenase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20210610 MGI PMID:31571584 10717 Hmox1 heme oxygenase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 10717 Hmox1 heme oxygenase 1 gene MP:0011352 proximal convoluted tubule brush border loss IAGP N RGD:5509061 20141003 MGI PMID:10807584 10717 Hmox1 heme oxygenase 1 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:10807584 10717 Hmox1 heme oxygenase 1 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20201022 MGI 10717 Hmox1 heme oxygenase 1 gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0011854 cerebral edema IAGP N RGD:5509061 20141003 MGI PMID:19706490 10717 Hmox1 heme oxygenase 1 gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20141003 MGI PMID:9380735 10717 Hmox1 heme oxygenase 1 gene MP:0020953 decreased susceptibility to Paramyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:19398754 10717 Hmox1 heme oxygenase 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:24995976 10717 Hmox1 heme oxygenase 1 gene MP:0031510 increased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:11385506 10718 Foxa1 forkhead box A1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18381283 10718 Foxa1 forkhead box A1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:10049364 10718 Foxa1 forkhead box A1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:10468578 10718 Foxa1 forkhead box A1 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:20501593 10718 Foxa1 forkhead box A1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10468578 10718 Foxa1 forkhead box A1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19141476 10718 Foxa1 forkhead box A1 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10049364 10718 Foxa1 forkhead box A1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10049364 10718 Foxa1 forkhead box A1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10468578 10718 Foxa1 forkhead box A1 gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20141003 MGI PMID:10049364 10718 Foxa1 forkhead box A1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:19141476 10718 Foxa1 forkhead box A1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10468578 10718 Foxa1 forkhead box A1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12395314 10718 Foxa1 forkhead box A1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10468578 10718 Foxa1 forkhead box A1 gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:10049364 10718 Foxa1 forkhead box A1 gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:10468578 10718 Foxa1 forkhead box A1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10468578 10718 Foxa1 forkhead box A1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:10468578 10718 Foxa1 forkhead box A1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22265403 10718 Foxa1 forkhead box A1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:19141476 10718 Foxa1 forkhead box A1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:19141476 10718 Foxa1 forkhead box A1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22265403 10718 Foxa1 forkhead box A1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22265403 10718 Foxa1 forkhead box A1 gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:10468578 10718 Foxa1 forkhead box A1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:10468578 10718 Foxa1 forkhead box A1 gene MP:0005492 exocrine pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19141476 10718 Foxa1 forkhead box A1 gene MP:0009111 pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19141476 10718 Foxa1 forkhead box A1 gene MP:0009169 pancreatic islet hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19141476 10718 Foxa1 forkhead box A1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10049364 10718 Foxa1 forkhead box A1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10468578 10718 Foxa1 forkhead box A1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19141476 10718 Foxa1 forkhead box A1 gene MP:0014126 increased mammary gland apoptosis IAGP N RGD:5509061 20160317 MGI PMID:20501593 10718 Foxa1 forkhead box A1 gene MP:0014161 increased circulating cortisol level IAGP N RGD:5509061 20160414 MGI PMID:10468578 10719 Foxa2 forkhead box A2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11445544 10719 Foxa2 forkhead box A2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:15680365 10719 Foxa2 forkhead box A2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:14757645 10719 Foxa2 forkhead box A2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:18832392 10719 Foxa2 forkhead box A2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11846474 10719 Foxa2 forkhead box A2 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15680365 10719 Foxa2 forkhead box A2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19956259 10719 Foxa2 forkhead box A2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15616563 10719 Foxa2 forkhead box A2 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15616563 10719 Foxa2 forkhead box A2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19141476 10719 Foxa2 forkhead box A2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9825865 10719 Foxa2 forkhead box A2 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20220203 MGI PMID:20484741 10719 Foxa2 forkhead box A2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11445544 10719 Foxa2 forkhead box A2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220203 MGI PMID:20484741 10719 Foxa2 forkhead box A2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220203 MGI PMID:20484741 10719 Foxa2 forkhead box A2 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:19141476 10719 Foxa2 forkhead box A2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11445544 10719 Foxa2 forkhead box A2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15616563 10719 Foxa2 forkhead box A2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11445544 10719 Foxa2 forkhead box A2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10866673 10719 Foxa2 forkhead box A2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17304540 10719 Foxa2 forkhead box A2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18161057 10719 Foxa2 forkhead box A2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23359409 10719 Foxa2 forkhead box A2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23712942 10719 Foxa2 forkhead box A2 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:11291865 10719 Foxa2 forkhead box A2 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0002234 abnormal pharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0002281 abnormal respiratory mucosa goblet cell morphology IAGP N RGD:5509061 20200402 MGI PMID:30923168 10719 Foxa2 forkhead box A2 gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20141003 MGI PMID:14757645 10719 Foxa2 forkhead box A2 gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20200402 MGI PMID:30923168 10719 Foxa2 forkhead box A2 gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:11445544 10719 Foxa2 forkhead box A2 gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:15680365 10719 Foxa2 forkhead box A2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19956259 10719 Foxa2 forkhead box A2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19956259 10719 Foxa2 forkhead box A2 gene MP:0002767 situs ambiguus IAGP N RGD:5509061 20141003 MGI PMID:8610012 10719 Foxa2 forkhead box A2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19956259 10719 Foxa2 forkhead box A2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22265403 10719 Foxa2 forkhead box A2 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:19141476 10719 Foxa2 forkhead box A2 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:11445544 10719 Foxa2 forkhead box A2 gene MP:0003653 decreased skin turgor IAGP N RGD:5509061 20141003 MGI PMID:15680365 10719 Foxa2 forkhead box A2 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220203 MGI PMID:20484741 10719 Foxa2 forkhead box A2 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:19141476 10719 Foxa2 forkhead box A2 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:22529374 10719 Foxa2 forkhead box A2 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:18161057 10719 Foxa2 forkhead box A2 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19956259 10719 Foxa2 forkhead box A2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:8610012 10719 Foxa2 forkhead box A2 gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:8610012 10719 Foxa2 forkhead box A2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22265403 10719 Foxa2 forkhead box A2 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22265403 10719 Foxa2 forkhead box A2 gene MP:0004554 small pharynx IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0004781 abnormal surfactant composition IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0004831 long incisors IAGP N RGD:5509061 20170928 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20200402 MGI PMID:30923168 10719 Foxa2 forkhead box A2 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11445544 10719 Foxa2 forkhead box A2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:11291865 10719 Foxa2 forkhead box A2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:15616563 10719 Foxa2 forkhead box A2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19956259 10719 Foxa2 forkhead box A2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19956259 10719 Foxa2 forkhead box A2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:14757645 10719 Foxa2 forkhead box A2 gene MP:0005440 increased glycogen level IAGP N RGD:5509061 20141003 MGI PMID:11445544 10719 Foxa2 forkhead box A2 gene MP:0005492 exocrine pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19141476 10719 Foxa2 forkhead box A2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19956259 10719 Foxa2 forkhead box A2 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:14757645 10719 Foxa2 forkhead box A2 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0006294 absent optic vesicle IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0006338 abnormal second pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:19956259 10719 Foxa2 forkhead box A2 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:19956259 10719 Foxa2 forkhead box A2 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20161027 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0009021 absent estrus IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0009096 decreased endometrial gland number IAGP N RGD:5509061 20220203 MGI PMID:20484741 10719 Foxa2 forkhead box A2 gene MP:0009111 pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19141476 10719 Foxa2 forkhead box A2 gene MP:0009163 absent pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:22529374 10719 Foxa2 forkhead box A2 gene MP:0009169 pancreatic islet hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19141476 10719 Foxa2 forkhead box A2 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22529374 10719 Foxa2 forkhead box A2 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:15680365 10719 Foxa2 forkhead box A2 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:11445544 10719 Foxa2 forkhead box A2 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:15680365 10719 Foxa2 forkhead box A2 gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:11846474 10719 Foxa2 forkhead box A2 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:11291865 10719 Foxa2 forkhead box A2 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15616563 10719 Foxa2 forkhead box A2 gene MP:0009667 abnormal embryo invasion IAGP N RGD:5509061 20220203 MGI PMID:20484741 10719 Foxa2 forkhead box A2 gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20220203 MGI PMID:20484741 10719 Foxa2 forkhead box A2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19956259 10719 Foxa2 forkhead box A2 gene MP:0010355 abnormal first pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20230706 MGI PMID:27606604 10719 Foxa2 forkhead box A2 gene MP:0010549 absent dorsal mesocardium IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0010814 absent alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0010817 absent type I pneumocytes IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:14757645 10719 Foxa2 forkhead box A2 gene MP:0010861 increased respiratory mucosa goblet cell number IAGP N RGD:5509061 20141003 MGI PMID:14757645 10719 Foxa2 forkhead box A2 gene MP:0010896 decreased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:14757645 10719 Foxa2 forkhead box A2 gene MP:0010935 increased airway resistance IAGP N RGD:5509061 20141003 MGI PMID:14757645 10719 Foxa2 forkhead box A2 gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0011018 pulmonary hyaline membrane formation IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11445544 10719 Foxa2 forkhead box A2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15680365 10719 Foxa2 forkhead box A2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19141476 10719 Foxa2 forkhead box A2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14757645 10719 Foxa2 forkhead box A2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18161057 10719 Foxa2 forkhead box A2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11846474 10719 Foxa2 forkhead box A2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:19956259 10719 Foxa2 forkhead box A2 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:19956259 10719 Foxa2 forkhead box A2 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:18161057 10719 Foxa2 forkhead box A2 gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:8069909 10719 Foxa2 forkhead box A2 gene MP:0012263 decreased hindbrain size IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0012271 abnormal chordamesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:8069910 10719 Foxa2 forkhead box A2 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:11291865 10719 Foxa2 forkhead box A2 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:9226455 10719 Foxa2 forkhead box A2 gene MP:0013400 abnormal endometrial gland development IAGP N RGD:5509061 20220203 MGI PMID:20484741 10719 Foxa2 forkhead box A2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:9825865 10719 Foxa2 forkhead box A2 gene MP:0014473 increased pulmonary alveolus wall thickness IAGP N RGD:5509061 20240704 MGI PMID:15452354 10719 Foxa2 forkhead box A2 gene MP:0031434 increased miscarriage rate IAGP N RGD:5509061 20220915 MGI PMID:8069910 10720 Foxa3 forkhead box A3 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20181220 MGI PMID:17488644 10720 Foxa3 forkhead box A3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20181220 MGI PMID:17488644 10720 Foxa3 forkhead box A3 gene MP:0001661 extended life span IAGP N RGD:5509061 20181220 MGI PMID:25225406 10720 Foxa3 forkhead box A3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20181220 MGI PMID:17488644 10720 Foxa3 forkhead box A3 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20181220 MGI PMID:25225406 10720 Foxa3 forkhead box A3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9632808 10720 Foxa3 forkhead box A3 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20181220 MGI PMID:17488644 10720 Foxa3 forkhead box A3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20181220 MGI PMID:25225406 10720 Foxa3 forkhead box A3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20181220 MGI PMID:17488644 10720 Foxa3 forkhead box A3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20181220 MGI PMID:25225406 10720 Foxa3 forkhead box A3 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20181220 MGI PMID:25225406 10720 Foxa3 forkhead box A3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20181220 MGI PMID:25225406 10720 Foxa3 forkhead box A3 gene MP:0008390 abnormal primordial germ cell proliferation IAGP N RGD:5509061 20181220 MGI PMID:17488644 10720 Foxa3 forkhead box A3 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20181220 MGI PMID:25225406 10720 Foxa3 forkhead box A3 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20181220 MGI PMID:25225406 10720 Foxa3 forkhead box A3 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20181220 MGI PMID:25225406 10720 Foxa3 forkhead box A3 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20181220 MGI PMID:17488644 10720 Foxa3 forkhead box A3 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20181220 MGI PMID:11546810 10720 Foxa3 forkhead box A3 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20181220 MGI PMID:17488644 10720 Foxa3 forkhead box A3 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20181220 MGI PMID:25225406 10720 Foxa3 forkhead box A3 gene MP:0020103 decreased hepatic glucose production IAGP N RGD:5509061 20181220 MGI PMID:11546810 10720 Foxa3 forkhead box A3 gene MP:0020325 abnormal beige fat cell morphology IAGP N RGD:5509061 20181220 MGI PMID:25225406 10720 Foxa3 forkhead box A3 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20181220 MGI PMID:25225406 10721 Onecut1 one cut domain, family member 1 gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:11934848 10721 Onecut1 one cut domain, family member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10825208 10721 Onecut1 one cut domain, family member 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:17400205 10721 Onecut1 one cut domain, family member 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:10825208 10721 Onecut1 one cut domain, family member 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10825208 10721 Onecut1 one cut domain, family member 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:11934848 10721 Onecut1 one cut domain, family member 1 gene MP:0003250 absent gallbladder IAGP N RGD:5509061 20141003 MGI PMID:11934848 10721 Onecut1 one cut domain, family member 1 gene MP:0003266 biliary cyst IAGP N RGD:5509061 20141003 MGI PMID:16103213 10721 Onecut1 one cut domain, family member 1 gene MP:0003334 pancreas fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:10825208 10721 Onecut1 one cut domain, family member 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20200123 MGI PMID:23926259 10721 Onecut1 one cut domain, family member 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:10825208 10721 Onecut1 one cut domain, family member 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:12781686 10721 Onecut1 one cut domain, family member 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:17400205 10721 Onecut1 one cut domain, family member 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10825208 10721 Onecut1 one cut domain, family member 1 gene MP:0005083 abnormal biliary tract morphology IAGP N RGD:5509061 20141003 MGI PMID:11934848 10721 Onecut1 one cut domain, family member 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:10825208 10721 Onecut1 one cut domain, family member 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:10825208 10721 Onecut1 one cut domain, family member 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10825208 10721 Onecut1 one cut domain, family member 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10825208 10721 Onecut1 one cut domain, family member 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:23926259 10721 Onecut1 one cut domain, family member 1 gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:23926259 10721 Onecut1 one cut domain, family member 1 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200123 MGI PMID:23926259 10721 Onecut1 one cut domain, family member 1 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20200123 MGI PMID:23926259 10721 Onecut1 one cut domain, family member 1 gene MP:0009111 pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12781686 10721 Onecut1 one cut domain, family member 1 gene MP:0009111 pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17400205 10721 Onecut1 one cut domain, family member 1 gene MP:0009143 abnormal pancreatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0009149 decreased pancreatic acinar cell number IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0009164 exocrine pancreas atrophy IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0009173 absent pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0009174 absent pancreatic beta cells IAGP N RGD:5509061 20150305 MGI PMID:17400205 10721 Onecut1 one cut domain, family member 1 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:10825208 10721 Onecut1 one cut domain, family member 1 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0009178 absent pancreatic alpha cells IAGP N RGD:5509061 20150305 MGI PMID:17400205 10721 Onecut1 one cut domain, family member 1 gene MP:0009181 decreased pancreatic delta cell number IAGP N RGD:5509061 20141003 MGI PMID:10825208 10721 Onecut1 one cut domain, family member 1 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:10825208 10721 Onecut1 one cut domain, family member 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10825208 10721 Onecut1 one cut domain, family member 1 gene MP:0011932 abnormal endocrine pancreas development IAGP N RGD:5509061 20150305 MGI PMID:17400205 10721 Onecut1 one cut domain, family member 1 gene MP:0011934 abnormal branching involved in pancreas development IAGP N RGD:5509061 20160324 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200123 MGI PMID:23926259 10721 Onecut1 one cut domain, family member 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200123 MGI PMID:23926259 10721 Onecut1 one cut domain, family member 1 gene MP:0012242 abnormal hepatoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:16103213 10721 Onecut1 one cut domain, family member 1 gene MP:0012246 abnormal hepatic cord morphology IAGP N RGD:5509061 20141003 MGI PMID:16103213 10721 Onecut1 one cut domain, family member 1 gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20160324 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0014092 abnormal pancreatic primary cilium morphology IAGP N RGD:5509061 20190718 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0014094 decreased pancreatic primary cilium number IAGP N RGD:5509061 20190718 MGI PMID:19766716 10721 Onecut1 one cut domain, family member 1 gene MP:0014108 calcified pancreas IAGP N RGD:5509061 20160324 MGI PMID:19766716 10724 Hoxc homeobox C cluster gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:10753520 10724 Hoxc homeobox C cluster gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20111116 MGI PMID:10753520 10724 Hoxc homeobox C cluster gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20111116 MGI PMID:10753520 10724 Hoxc homeobox C cluster gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20111116 MGI PMID:10753520 10724 Hoxc homeobox C cluster gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:10753520 10724 Hoxc homeobox C cluster gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:10753520 10724 Hoxc homeobox C cluster gene MP:0004614 caudal vertebral transformation IAGP N RGD:5509061 20111116 MGI PMID:10753520 10724 Hoxc homeobox C cluster gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20111116 MGI PMID:10753520 10724 Hoxc homeobox C cluster gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20111116 MGI PMID:10753520 10724 Hoxc homeobox C cluster gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20111116 MGI PMID:10753520 10724 Hoxc homeobox C cluster gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20111116 MGI PMID:10753520 10728 Hp haptoglobin gene MP:0000332 hemoglobinemia IAGP N RGD:5509061 20141003 MGI PMID:9731043 10728 Hp haptoglobin gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12393471 10728 Hp haptoglobin gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:12393471 10728 Hp haptoglobin gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:9731043 10728 Hp haptoglobin gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15793279 10728 Hp haptoglobin gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:9731043 10728 Hp haptoglobin gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20141003 MGI PMID:17082477 10728 Hp haptoglobin gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:19176700 10728 Hp haptoglobin gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19176700 10728 Hp haptoglobin gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:19176700 10728 Hp haptoglobin gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17068284 10728 Hp haptoglobin gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:12393471 10728 Hp haptoglobin gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:19176700 10728 Hp haptoglobin gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:12393471 10728 Hp haptoglobin gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12393471 10728 Hp haptoglobin gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9731043 10728 Hp haptoglobin gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12393471 10728 Hp haptoglobin gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11865977 10728 Hp haptoglobin gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20141003 MGI PMID:15793279 10728 Hp haptoglobin gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17068284 10728 Hp haptoglobin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9731043 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0000091 short premaxilla IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:24057668 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:19416908 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:19416908 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:19416908 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12427827 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19416908 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:19416908 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:19416908 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19416908 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11238881 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18059342 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:24057668 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0002649 abnormal enamel rod pattern IAGP N RGD:5509061 20141003 MGI PMID:24057668 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:19416908 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:24057668 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0003108 short zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19416908 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0003404 absent enamel IAGP N RGD:5509061 20141003 MGI PMID:24057668 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19416908 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0003769 abnormal lip morphology IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:10871846 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19416908 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20160811 MGI PMID:26359368 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0010591 enlarged aortic valve IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19416908 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18059342 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18059342 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0012080 chylous ascites IAGP N RGD:5509061 20141003 MGI PMID:20179099 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0030034 depressed nasal bridge IAGP N RGD:5509061 20170914 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0030036 short nasal bridge IAGP N RGD:5509061 20170914 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0030062 choanal stenosis IAGP N RGD:5509061 20170921 MGI PMID:18483625 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0030199 deviated nasal septum IAGP N RGD:5509061 20171012 MGI PMID:19416908 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0030219 jaw cyst IAGP N RGD:5509061 20171019 MGI PMID:24057668 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20171221 MGI PMID:19416908 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20171221 MGI PMID:24057668 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0030471 abnormal ameloblast differentiation IAGP N RGD:5509061 20180118 MGI PMID:24057668 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0030521 abnormal cervical loop morphology IAGP N RGD:5509061 20180118 MGI PMID:24057668 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0030522 abnormal stellate reticulum morphology IAGP N RGD:5509061 20180118 MGI PMID:24057668 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0030523 abnormal stratum intermedium morphology IAGP N RGD:5509061 20180118 MGI PMID:24057668 10730 Hras Harvey rat sarcoma virus oncogene gene MP:0031232 increased circulating angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:18483625 10731 Hrh1 histamine receptor H1 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15331534 10731 Hrh1 histamine receptor H1 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15331534 10731 Hrh1 histamine receptor H1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15331534 10731 Hrh1 histamine receptor H1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15331534 10731 Hrh1 histamine receptor H1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:8917588 10731 Hrh1 histamine receptor H1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15331534 10731 Hrh1 histamine receptor H1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20150129 MGI PMID:12142541 10731 Hrh1 histamine receptor H1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9989982 10731 Hrh1 histamine receptor H1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16680192 10731 Hrh1 histamine receptor H1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 10731 Hrh1 histamine receptor H1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20150129 MGI PMID:12142541 10731 Hrh1 histamine receptor H1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16680192 10731 Hrh1 histamine receptor H1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16680192 10731 Hrh1 histamine receptor H1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15331534 10731 Hrh1 histamine receptor H1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:8917588 10731 Hrh1 histamine receptor H1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:15331534 10731 Hrh1 histamine receptor H1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:8917588 10731 Hrh1 histamine receptor H1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9989982 10731 Hrh1 histamine receptor H1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20150129 MGI PMID:12142541 10731 Hrh1 histamine receptor H1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9989982 10731 Hrh1 histamine receptor H1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9989982 10731 Hrh1 histamine receptor H1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15331534 10731 Hrh1 histamine receptor H1 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:15331534 10731 Hrh1 histamine receptor H1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9989982 10731 Hrh1 histamine receptor H1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16680192 10731 Hrh1 histamine receptor H1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9989982 10731 Hrh1 histamine receptor H1 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:16680192 10731 Hrh1 histamine receptor H1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:9989982 10731 Hrh1 histamine receptor H1 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:9989982 10731 Hrh1 histamine receptor H1 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:16680192 10731 Hrh1 histamine receptor H1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15331534 10731 Hrh1 histamine receptor H1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20150129 MGI PMID:12142541 10731 Hrh1 histamine receptor H1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15331534 10731 Hrh1 histamine receptor H1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:15331534 10731 Hrh1 histamine receptor H1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:15331534 10731 Hrh1 histamine receptor H1 gene MP:0011943 abnormal circadian feeding behavior IAGP N RGD:5509061 20141003 MGI PMID:15331534 10731 Hrh1 histamine receptor H1 gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20171012 MGI PMID:8917588 10731 Hrh1 histamine receptor H1 gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:15331534 10732 Hrh2 histamine receptor H2 gene MP:0000505 decreased digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:10862789 10732 Hrh2 histamine receptor H2 gene MP:0000505 decreased digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:12729842 10732 Hrh2 histamine receptor H2 gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20141003 MGI PMID:12729842 10732 Hrh2 histamine receptor H2 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12729842 10732 Hrh2 histamine receptor H2 gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:12729842 10732 Hrh2 histamine receptor H2 gene MP:0003892 abnormal gastric gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12729842 10732 Hrh2 histamine receptor H2 gene MP:0004138 abnormal mucous neck cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12729842 10732 Hrh2 histamine receptor H2 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10862789 10732 Hrh2 histamine receptor H2 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12729842 10732 Hrh2 histamine receptor H2 gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12729842 10732 Hrh2 histamine receptor H2 gene MP:0004731 increased circulating gastrin level IAGP N RGD:5509061 20141003 MGI PMID:10862789 10732 Hrh2 histamine receptor H2 gene MP:0004731 increased circulating gastrin level IAGP N RGD:5509061 20141003 MGI PMID:12729842 10732 Hrh2 histamine receptor H2 gene MP:0005211 increased stomach mucosa thickness IAGP N RGD:5509061 20141003 MGI PMID:10862789 10732 Hrh2 histamine receptor H2 gene MP:0008004 abnormal stomach pH IAGP N RGD:5509061 20141003 MGI PMID:10862789 10732 Hrh2 histamine receptor H2 gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20141003 MGI PMID:12729842 10732 Hrh2 histamine receptor H2 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10862789 10732 Hrh2 histamine receptor H2 gene MP:0010799 stomach mucosa hyperplasia IAGP N RGD:5509061 20150312 MGI PMID:12729842 10732 Hrh2 histamine receptor H2 gene MP:0013569 gastric gland hyperplasia IAGP N RGD:5509061 20150312 MGI PMID:12729842 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15047607 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11546766 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15047607 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:21106871 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:22555437 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:9405715 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:11274359 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:12439781 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21106871 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22555437 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11274359 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:23383297 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11546766 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15047607 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22555437 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23832962 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20151224 MGI PMID:24667799 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0002078 abnormal glucose homeostasis IEA N RGD:5509061 20111116 MGI 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11546766 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12439781 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:11546766 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11546766 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:22555437 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22555437 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:23383297 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21106871 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:23383297 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:21106871 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:11165006 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:9405715 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20151224 MGI PMID:24667799 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23383297 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11546766 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:11274359 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22555437 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11546766 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15047607 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:23383297 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:24169553 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21106871 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:9405715 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:18779947 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15047607 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:23832962 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0008243 abnormal macrophage derived foam cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23383297 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23383297 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23383297 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:21106871 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:21106871 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0009428 decreased tibialis anterior weight IAGP N RGD:5509061 20141003 MGI PMID:21106871 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:23832962 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:21106871 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:9405715 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:21106871 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0010814 absent alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:12439781 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0010889 small alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:12439781 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0010890 decreased alveolar lamellar body number IAGP N RGD:5509061 20141003 MGI PMID:12439781 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20151224 MGI PMID:24667799 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:12439781 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0011702 abnormal fibroblast proliferation IAGP N RGD:5509061 20151224 MGI PMID:24667799 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20151224 MGI PMID:24667799 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:24169553 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0012172 abnormal amniotic fluid composition IAGP N RGD:5509061 20141003 MGI PMID:12439781 10734 Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20151224 MGI PMID:24667799 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16896181 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23741059 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23741059 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:23741059 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0005628 decreased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0009051 dilated distal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10074485 10735 Hsd11b2 hydroxysteroid 11-beta dehydrogenase 2 gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:10074485 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20160602 MGI PMID:26018678 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20190502 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0001523 impaired righting response IEA N RGD:5509061 20170105 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20160602 MGI PMID:26018678 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20160602 MGI PMID:26018678 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20160602 MGI PMID:26018678 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20160602 MGI PMID:26018678 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20160602 MGI PMID:26018678 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20211021 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20170105 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210520 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0004855 increased ovary weight IAGP N RGD:5509061 20160602 MGI PMID:26018678 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0004903 abnormal uterus weight IAGP N RGD:5509061 20160602 MGI PMID:26018678 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0005133 increased luteinizing hormone level IAGP N RGD:5509061 20160602 MGI PMID:26018678 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170105 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20170105 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0011384 abnormal progesterone level IAGP N RGD:5509061 20160602 MGI PMID:26018678 10736 Hsd17b1 hydroxysteroid (17-beta) dehydrogenase 1 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20170105 MGI 10740 Hspa2 heat shock protein 2 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:8622925 10740 Hspa2 heat shock protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8622925 10740 Hspa2 heat shock protein 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:8622925 10740 Hspa2 heat shock protein 2 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:8622925 10742 Hspa5 heat shock protein 5 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21214893 10742 Hspa5 heat shock protein 5 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:21214893 10742 Hspa5 heat shock protein 5 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21214893 10742 Hspa5 heat shock protein 5 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:21214893 10742 Hspa5 heat shock protein 5 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:17464327 10742 Hspa5 heat shock protein 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 10742 Hspa5 heat shock protein 5 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17464327 10742 Hspa5 heat shock protein 5 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17464327 10742 Hspa5 heat shock protein 5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:21214893 10742 Hspa5 heat shock protein 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16847323 10742 Hspa5 heat shock protein 5 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17464327 10742 Hspa5 heat shock protein 5 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17464327 10742 Hspa5 heat shock protein 5 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18158912 10742 Hspa5 heat shock protein 5 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18158912 10742 Hspa5 heat shock protein 5 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:21214893 10742 Hspa5 heat shock protein 5 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 10742 Hspa5 heat shock protein 5 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:21214893 10742 Hspa5 heat shock protein 5 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20211021 MGI 10742 Hspa5 heat shock protein 5 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18158912 10742 Hspa5 heat shock protein 5 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:21214893 10742 Hspa5 heat shock protein 5 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:16847323 10742 Hspa5 heat shock protein 5 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17464327 10742 Hspa5 heat shock protein 5 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:17464327 10742 Hspa5 heat shock protein 5 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:17464327 10742 Hspa5 heat shock protein 5 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:16847323 10742 Hspa5 heat shock protein 5 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:18158912 10742 Hspa5 heat shock protein 5 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 10742 Hspa5 heat shock protein 5 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21214893 10742 Hspa5 heat shock protein 5 gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0008817 hematoma IAGP N RGD:5509061 20141003 MGI PMID:21214893 10742 Hspa5 heat shock protein 5 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:19033462 10742 Hspa5 heat shock protein 5 gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19033462 10742 Hspa5 heat shock protein 5 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:21214893 10742 Hspa5 heat shock protein 5 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20141003 MGI PMID:16847323 10742 Hspa5 heat shock protein 5 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16847323 10742 Hspa5 heat shock protein 5 gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:17464327 10742 Hspa5 heat shock protein 5 gene MP:0010909 pulmonary alveolar hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17464327 10742 Hspa5 heat shock protein 5 gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17464327 10742 Hspa5 heat shock protein 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21214893 10742 Hspa5 heat shock protein 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22821687 10742 Hspa5 heat shock protein 5 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16847323 10742 Hspa5 heat shock protein 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10742 Hspa5 heat shock protein 5 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:18158912 10742 Hspa5 heat shock protein 5 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:16847323 10742 Hspa5 heat shock protein 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 10742 Hspa5 heat shock protein 5 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10751426 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20152131 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:9724773 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:9826725 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:9844013 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11121072 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:23997373 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:11080193 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18599790 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:9826725 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:9844013 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:16507009 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:9844013 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:11121072 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:10751426 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:11121072 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:20152131 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18599790 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:11080193 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:11483665 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:18599790 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:18599790 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0006276 abnormal autonomic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18599790 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18599790 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0009436 fragmentation of sleep/wake states IAGP N RGD:5509061 20220922 MGI PMID:23997373 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0012287 increased frequency of paradoxical sleep IAGP N RGD:5509061 20141003 MGI PMID:23997373 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0012291 increased slow-wave sleep duration IAGP N RGD:5509061 20141003 MGI PMID:23997373 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:11080193 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0021198 abnormal sleep duration IAGP N RGD:5509061 20220922 MGI PMID:23997373 10745 Htr1a 5-hydroxytryptamine (serotonin) receptor 1A gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:9724773 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16380550 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11790410 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11164514 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11790410 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:8091214 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10996411 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12798274 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:11164514 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:16380550 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12742250 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0002833 increased heart weight IEA N RGD:5509061 20220519 MGI 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16380550 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:12798274 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0003958 heart valve hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16380550 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160421 MGI 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:19041748 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16380550 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:19041748 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:11790410 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:19041748 10746 Htr1b 5-hydroxytryptamine (serotonin) receptor 1B gene MP:0030438 increased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:19041748 10747 Htr1d 5-hydroxytryptamine (serotonin) receptor 1D gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 10747 Htr1d 5-hydroxytryptamine (serotonin) receptor 1D gene MP:0005379 endocrine/exocrine gland phenotype IAGP N RGD:5509061 20200402 MGI PMID:31806625 10747 Htr1d 5-hydroxytryptamine (serotonin) receptor 1D gene MP:0010053 decreased grip strength IEA N RGD:5509061 20221215 MGI 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19038216 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:7700379 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:9771748 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0000421 mottled coat IAGP N RGD:5509061 20141003 MGI PMID:20394819 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:7700379 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:20394819 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:7700379 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20394819 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19038216 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20394819 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:9844009 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:20394819 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:19038216 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:7700379 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:9771748 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:7700379 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:9844009 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:9844009 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20141003 MGI PMID:20394819 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:20394819 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:9771748 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20394819 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20160317 MGI PMID:25257581 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9771748 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19038216 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7700379 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:7700379 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:7700379 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0003063 increased coping response IAGP N RGD:5509061 20160317 MGI PMID:25257581 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:9771748 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:9771748 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19038216 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19038216 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:7700379 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20160317 MGI PMID:25257581 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:20394819 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:20394819 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:9771748 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:9771748 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:19038216 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005535 abnormal body temperature IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19038216 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:9771748 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19038216 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:9771748 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:9771748 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:7700379 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:9771748 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:7700379 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:9771748 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19038216 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:7700379 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20394819 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20394819 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20394819 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0011612 increased circulating ghrelin level IAGP N RGD:5509061 20141003 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:20394819 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:24177424 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:20394819 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20160414 MGI PMID:19036977 10748 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:19036977 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0001761 abnormal urination pattern IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0003043 hypoalgesia IEA N RGD:5509061 20220519 MGI 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0003280 urinary incontinence IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0003608 prostate gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0005302 neurogenic bladder IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11826129 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0009552 urinary bladder obstruction IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0011403 pyelonephritis IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0011774 abnormal urinary bladder detrusor smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0011777 abnormal male prostatic urethra morphology IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0011784 abnormal urinary bladder neck morphology IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0011799 increased urinary bladder weight IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0011801 urethra obstruction IAGP N RGD:5509061 20141003 MGI PMID:15201326 10749 Htr3a 5-hydroxytryptamine (serotonin) receptor 3A gene MP:0011802 seminal vesiculitis IAGP N RGD:5509061 20141003 MGI PMID:15201326 10750 Htr4 5 hydroxytryptamine (serotonin) receptor 4 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:14724239 10750 Htr4 5 hydroxytryptamine (serotonin) receptor 4 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:14724239 10750 Htr4 5 hydroxytryptamine (serotonin) receptor 4 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:14724239 10750 Htr4 5 hydroxytryptamine (serotonin) receptor 4 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:14724239 10750 Htr4 5 hydroxytryptamine (serotonin) receptor 4 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:14724239 10750 Htr4 5 hydroxytryptamine (serotonin) receptor 4 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:14724239 10750 Htr4 5 hydroxytryptamine (serotonin) receptor 4 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20180531 MGI PMID:17913892 10750 Htr4 5 hydroxytryptamine (serotonin) receptor 4 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20111116 MGI 10750 Htr4 5 hydroxytryptamine (serotonin) receptor 4 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180531 MGI PMID:17913892 10750 Htr4 5 hydroxytryptamine (serotonin) receptor 4 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14724239 10751 Htr5a 5-hydroxytryptamine (serotonin) receptor 5A gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:10197537 10751 Htr5a 5-hydroxytryptamine (serotonin) receptor 5A gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 10751 Htr5a 5-hydroxytryptamine (serotonin) receptor 5A gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:10197537 10754 Iapp islet amyloid polypeptide gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:14970190 10754 Iapp islet amyloid polypeptide gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:14970190 10754 Iapp islet amyloid polypeptide gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14970190 10754 Iapp islet amyloid polypeptide gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:14970190 10754 Iapp islet amyloid polypeptide gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:9753619 10754 Iapp islet amyloid polypeptide gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9753619 10754 Iapp islet amyloid polypeptide gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:14970190 10754 Iapp islet amyloid polypeptide gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:14970190 10754 Iapp islet amyloid polypeptide gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:14970190 10754 Iapp islet amyloid polypeptide gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:9753619 10754 Iapp islet amyloid polypeptide gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:14970190 10754 Iapp islet amyloid polypeptide gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:14970190 10755 Ibsp integrin binding sialoprotein gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0000120 malocclusion IAGP N RGD:5509061 20180201 MGI PMID:23183644 10755 Ibsp integrin binding sialoprotein gene MP:0000120 malocclusion IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0003668 abnormal periodontal ligament morphology IAGP N RGD:5509061 20180125 MGI PMID:23183644 10755 Ibsp integrin binding sialoprotein gene MP:0003668 abnormal periodontal ligament morphology IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20160804 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20160804 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20160804 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20180125 MGI PMID:23183644 10755 Ibsp integrin binding sialoprotein gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20160804 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20160804 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20160804 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0010924 abnormal osteoid morphology IAGP N RGD:5509061 20160804 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0010924 abnormal osteoid morphology IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0010929 increased osteoid thickness IAGP N RGD:5509061 20160804 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0011165 abnormal tooth root development IAGP N RGD:5509061 20180125 MGI PMID:23183644 10755 Ibsp integrin binding sialoprotein gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20220915 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20160804 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:18458111 10755 Ibsp integrin binding sialoprotein gene MP:0030131 abnormal periodontium morphology IAGP N RGD:5509061 20180125 MGI PMID:23183644 10755 Ibsp integrin binding sialoprotein gene MP:0030351 wide coronal suture IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0030357 wide lambdoid suture IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0030393 delayed fontanelle closure IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0030452 abnormal cementum mineralization IAGP N RGD:5509061 20180125 MGI PMID:23183644 10755 Ibsp integrin binding sialoprotein gene MP:0030466 alveolar process atrophy IAGP N RGD:5509061 20180125 MGI PMID:23183644 10755 Ibsp integrin binding sialoprotein gene MP:0030466 alveolar process atrophy IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0030494 abnormal molar root morphology IAGP N RGD:5509061 20180125 MGI PMID:23183644 10755 Ibsp integrin binding sialoprotein gene MP:0030516 abnormal junctional epithelium morphology IAGP N RGD:5509061 20180125 MGI PMID:23183644 10755 Ibsp integrin binding sialoprotein gene MP:0030524 abnormal tooth root resorption IAGP N RGD:5509061 20180125 MGI PMID:23183644 10755 Ibsp integrin binding sialoprotein gene MP:0030524 abnormal tooth root resorption IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20180125 MGI PMID:23183644 10755 Ibsp integrin binding sialoprotein gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20180201 MGI PMID:25963390 10755 Ibsp integrin binding sialoprotein gene MP:0030545 abnormal acellular cementum morphology IAGP N RGD:5509061 20180208 MGI PMID:23183644 10755 Ibsp integrin binding sialoprotein gene MP:0030545 abnormal acellular cementum morphology IAGP N RGD:5509061 20180208 MGI PMID:25963390 10756 Icam1 intercellular adhesion molecule 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11375415 10756 Icam1 intercellular adhesion molecule 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14634125 10756 Icam1 intercellular adhesion molecule 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8551244 10756 Icam1 intercellular adhesion molecule 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10228023 10756 Icam1 intercellular adhesion molecule 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11375415 10756 Icam1 intercellular adhesion molecule 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:14634125 10756 Icam1 intercellular adhesion molecule 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:7535798 10756 Icam1 intercellular adhesion molecule 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:7911822 10756 Icam1 intercellular adhesion molecule 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8104338 10756 Icam1 intercellular adhesion molecule 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9636189 10756 Icam1 intercellular adhesion molecule 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11375415 10756 Icam1 intercellular adhesion molecule 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9636189 10756 Icam1 intercellular adhesion molecule 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:9636189 10756 Icam1 intercellular adhesion molecule 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:12766082 10756 Icam1 intercellular adhesion molecule 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:15231732 10756 Icam1 intercellular adhesion molecule 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:10670575 10756 Icam1 intercellular adhesion molecule 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:10228023 10756 Icam1 intercellular adhesion molecule 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:8104338 10756 Icam1 intercellular adhesion molecule 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:17595378 10756 Icam1 intercellular adhesion molecule 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17595378 10756 Icam1 intercellular adhesion molecule 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15231732 10756 Icam1 intercellular adhesion molecule 1 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17595378 10756 Icam1 intercellular adhesion molecule 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7911822 10756 Icam1 intercellular adhesion molecule 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:15229332 10756 Icam1 intercellular adhesion molecule 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17595378 10756 Icam1 intercellular adhesion molecule 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15231732 10756 Icam1 intercellular adhesion molecule 1 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:17595378 10756 Icam1 intercellular adhesion molecule 1 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16934241 10756 Icam1 intercellular adhesion molecule 1 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:17291995 10756 Icam1 intercellular adhesion molecule 1 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:7535798 10756 Icam1 intercellular adhesion molecule 1 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:16731772 10756 Icam1 intercellular adhesion molecule 1 gene MP:0003434 decreased susceptibility to induced choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:12766082 10756 Icam1 intercellular adhesion molecule 1 gene MP:0003627 abnormal leukocyte tethering or rolling IAGP N RGD:5509061 20141003 MGI PMID:14634125 10756 Icam1 intercellular adhesion molecule 1 gene MP:0003627 abnormal leukocyte tethering or rolling IAGP N RGD:5509061 20141003 MGI PMID:8551244 10756 Icam1 intercellular adhesion molecule 1 gene MP:0003627 abnormal leukocyte tethering or rolling IAGP N RGD:5509061 20141003 MGI PMID:9636189 10756 Icam1 intercellular adhesion molecule 1 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:14634125 10756 Icam1 intercellular adhesion molecule 1 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:16412045 10756 Icam1 intercellular adhesion molecule 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17595378 10756 Icam1 intercellular adhesion molecule 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20160128 MGI PMID:26034041 10756 Icam1 intercellular adhesion molecule 1 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17291995 10756 Icam1 intercellular adhesion molecule 1 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:11120869 10756 Icam1 intercellular adhesion molecule 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9636189 10756 Icam1 intercellular adhesion molecule 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11375415 10756 Icam1 intercellular adhesion molecule 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7911822 10756 Icam1 intercellular adhesion molecule 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9636189 10756 Icam1 intercellular adhesion molecule 1 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:10228023 10756 Icam1 intercellular adhesion molecule 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11375415 10756 Icam1 intercellular adhesion molecule 1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:15231732 10756 Icam1 intercellular adhesion molecule 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11375415 10756 Icam1 intercellular adhesion molecule 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15231732 10756 Icam1 intercellular adhesion molecule 1 gene MP:0005580 periinsulitis IAGP N RGD:5509061 20141003 MGI PMID:11120869 10756 Icam1 intercellular adhesion molecule 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17291995 10756 Icam1 intercellular adhesion molecule 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17595378 10756 Icam1 intercellular adhesion molecule 1 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:7911822 10756 Icam1 intercellular adhesion molecule 1 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:8104338 10756 Icam1 intercellular adhesion molecule 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17291995 10756 Icam1 intercellular adhesion molecule 1 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:16731772 10756 Icam1 intercellular adhesion molecule 1 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:10228023 10756 Icam1 intercellular adhesion molecule 1 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10228023 10756 Icam1 intercellular adhesion molecule 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12847222 10756 Icam1 intercellular adhesion molecule 1 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:7911822 10756 Icam1 intercellular adhesion molecule 1 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:7911822 10756 Icam1 intercellular adhesion molecule 1 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:7911822 10756 Icam1 intercellular adhesion molecule 1 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:8104338 10756 Icam1 intercellular adhesion molecule 1 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:9636189 10756 Icam1 intercellular adhesion molecule 1 gene MP:0010751 decreased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12769195 10756 Icam1 intercellular adhesion molecule 1 gene MP:0011825 decreased cell chemotaxis IAGP N RGD:5509061 20160128 MGI PMID:26034041 10756 Icam1 intercellular adhesion molecule 1 gene MP:0012194 decreased keratinocyte migration IAGP N RGD:5509061 20141204 MGI PMID:17595378 10756 Icam1 intercellular adhesion molecule 1 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:8551244 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20150528 MGI PMID:25730874 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20150528 MGI PMID:25730874 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0001265 decreased body size IAGP N RGD:5509061 20150528 MGI PMID:25730874 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20150528 MGI PMID:25730874 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20150528 MGI PMID:25730874 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22763442 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20150528 MGI PMID:25730874 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20150528 MGI PMID:25730874 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 10758 Idh1 isocitrate dehydrogenase 1 (NADP+), soluble gene MP:0012514 pectus excavatum IAGP N RGD:5509061 20150528 MGI PMID:25730874 10759 Idh3g isocitrate dehydrogenase 3 (NAD+), gamma gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 10765 Igf1 insulin-like growth factor 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:11567053 10765 Igf1 insulin-like growth factor 1 gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:11567053 10765 Igf1 insulin-like growth factor 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:8402901 10765 Igf1 insulin-like growth factor 1 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11133160 10765 Igf1 insulin-like growth factor 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11133160 10765 Igf1 insulin-like growth factor 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11133160 10765 Igf1 insulin-like growth factor 1 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:12235108 10765 Igf1 insulin-like growth factor 1 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:15597051 10765 Igf1 insulin-like growth factor 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:11567053 10765 Igf1 insulin-like growth factor 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:15597051 10765 Igf1 insulin-like growth factor 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:11567053 10765 Igf1 insulin-like growth factor 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:20382057 10765 Igf1 insulin-like growth factor 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0001238 thin epidermis stratum spinosum IAGP N RGD:5509061 20141003 MGI PMID:8402901 10765 Igf1 insulin-like growth factor 1 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:10537147 10765 Igf1 insulin-like growth factor 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12235108 10765 Igf1 insulin-like growth factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11567053 10765 Igf1 insulin-like growth factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14741342 10765 Igf1 insulin-like growth factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19033454 10765 Igf1 insulin-like growth factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8958230 10765 Igf1 insulin-like growth factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8402901 10765 Igf1 insulin-like growth factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11133160 10765 Igf1 insulin-like growth factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11567053 10765 Igf1 insulin-like growth factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19033454 10765 Igf1 insulin-like growth factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8402901 10765 Igf1 insulin-like growth factor 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:19033454 10765 Igf1 insulin-like growth factor 1 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:20382057 10765 Igf1 insulin-like growth factor 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:8402901 10765 Igf1 insulin-like growth factor 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10537147 10765 Igf1 insulin-like growth factor 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10537147 10765 Igf1 insulin-like growth factor 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20048072 10765 Igf1 insulin-like growth factor 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8276243 10765 Igf1 insulin-like growth factor 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9731712 10765 Igf1 insulin-like growth factor 1 gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:8276243 10765 Igf1 insulin-like growth factor 1 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:8276243 10765 Igf1 insulin-like growth factor 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8276243 10765 Igf1 insulin-like growth factor 1 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12235108 10765 Igf1 insulin-like growth factor 1 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:8276243 10765 Igf1 insulin-like growth factor 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:8276243 10765 Igf1 insulin-like growth factor 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:7718235 10765 Igf1 insulin-like growth factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10377413 10765 Igf1 insulin-like growth factor 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:11567053 10765 Igf1 insulin-like growth factor 1 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:8958230 10765 Igf1 insulin-like growth factor 1 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11567053 10765 Igf1 insulin-like growth factor 1 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:11567053 10765 Igf1 insulin-like growth factor 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:12235108 10765 Igf1 insulin-like growth factor 1 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:8402901 10765 Igf1 insulin-like growth factor 1 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11567053 10765 Igf1 insulin-like growth factor 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11567053 10765 Igf1 insulin-like growth factor 1 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11133160 10765 Igf1 insulin-like growth factor 1 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12235108 10765 Igf1 insulin-like growth factor 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11133160 10765 Igf1 insulin-like growth factor 1 gene MP:0003429 insensitivity to growth hormone IAGP N RGD:5509061 20141003 MGI PMID:10537147 10765 Igf1 insulin-like growth factor 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20048072 10765 Igf1 insulin-like growth factor 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:7718235 10765 Igf1 insulin-like growth factor 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:11133160 10765 Igf1 insulin-like growth factor 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:12235108 10765 Igf1 insulin-like growth factor 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:19033454 10765 Igf1 insulin-like growth factor 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:17535874 10765 Igf1 insulin-like growth factor 1 gene MP:0003956 abnormal body size IAGP N RGD:5509061 20141003 MGI PMID:10537147 10765 Igf1 insulin-like growth factor 1 gene MP:0003986 small cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:11567053 10765 Igf1 insulin-like growth factor 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9731712 10765 Igf1 insulin-like growth factor 1 gene MP:0004664 delayed inner ear development IAGP N RGD:5509061 20141003 MGI PMID:11567053 10765 Igf1 insulin-like growth factor 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:10359843 10765 Igf1 insulin-like growth factor 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:17535874 10765 Igf1 insulin-like growth factor 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:19033454 10765 Igf1 insulin-like growth factor 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:20048072 10765 Igf1 insulin-like growth factor 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:20382057 10765 Igf1 insulin-like growth factor 1 gene MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:14741342 10765 Igf1 insulin-like growth factor 1 gene MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0004716 abnormal cochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11567053 10765 Igf1 insulin-like growth factor 1 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:16420467 10765 Igf1 insulin-like growth factor 1 gene MP:0004750 syndromic hearing loss IAGP N RGD:5509061 20141003 MGI PMID:16420467 10765 Igf1 insulin-like growth factor 1 gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:8958230 10765 Igf1 insulin-like growth factor 1 gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:10537147 10765 Igf1 insulin-like growth factor 1 gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:11133160 10765 Igf1 insulin-like growth factor 1 gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:17535874 10765 Igf1 insulin-like growth factor 1 gene MP:0005137 increased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:14741342 10765 Igf1 insulin-like growth factor 1 gene MP:0005158 ovary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10537147 10765 Igf1 insulin-like growth factor 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:8958230 10765 Igf1 insulin-like growth factor 1 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:17535874 10765 Igf1 insulin-like growth factor 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:14741342 10765 Igf1 insulin-like growth factor 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:20048072 10765 Igf1 insulin-like growth factor 1 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:14741342 10765 Igf1 insulin-like growth factor 1 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:8958230 10765 Igf1 insulin-like growth factor 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17535874 10765 Igf1 insulin-like growth factor 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:8958230 10765 Igf1 insulin-like growth factor 1 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:17535874 10765 Igf1 insulin-like growth factor 1 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:12235108 10765 Igf1 insulin-like growth factor 1 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:19033454 10765 Igf1 insulin-like growth factor 1 gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:12235108 10765 Igf1 insulin-like growth factor 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:10537147 10765 Igf1 insulin-like growth factor 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:14741342 10765 Igf1 insulin-like growth factor 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:9731712 10765 Igf1 insulin-like growth factor 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19033454 10765 Igf1 insulin-like growth factor 1 gene MP:0008831 abnormal insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:11133160 10765 Igf1 insulin-like growth factor 1 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0009014 prolonged proestrus IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0009018 short estrus IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0009090 myometrium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0009091 endometrium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0009096 decreased endometrial gland number IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14741342 10765 Igf1 insulin-like growth factor 1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:14741342 10765 Igf1 insulin-like growth factor 1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0009364 abnormal mature ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:10537147 10765 Igf1 insulin-like growth factor 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:20382057 10765 Igf1 insulin-like growth factor 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:8402901 10765 Igf1 insulin-like growth factor 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0009946 abnormal olfactory bulb layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0009947 abnormal olfactory bulb external plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0009951 abnormal olfactory bulb mitral cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0009954 abnormal mitral cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0010817 absent type I pneumocytes IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:20382057 10765 Igf1 insulin-like growth factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11846487 10765 Igf1 insulin-like growth factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10537147 10765 Igf1 insulin-like growth factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16420467 10765 Igf1 insulin-like growth factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12591604 10765 Igf1 insulin-like growth factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20382057 10765 Igf1 insulin-like growth factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8402901 10765 Igf1 insulin-like growth factor 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19033454 10765 Igf1 insulin-like growth factor 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11846487 10765 Igf1 insulin-like growth factor 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9731712 10765 Igf1 insulin-like growth factor 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10537147 10765 Igf1 insulin-like growth factor 1 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:16420467 10765 Igf1 insulin-like growth factor 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16420467 10765 Igf1 insulin-like growth factor 1 gene MP:0013400 abnormal endometrial gland development IAGP N RGD:5509061 20141218 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0031421 increased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:19497975 10765 Igf1 insulin-like growth factor 1 gene MP:0031635 increased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:8958230 10766 Igf1r insulin-like growth factor I receptor gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12215457 10766 Igf1r insulin-like growth factor I receptor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0000380 small hair follicles IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:11846487 10766 Igf1r insulin-like growth factor I receptor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11818962 10766 Igf1r insulin-like growth factor I receptor gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:18443199 10766 Igf1r insulin-like growth factor I receptor gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:12930811 10766 Igf1r insulin-like growth factor I receptor gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12930811 10766 Igf1r insulin-like growth factor I receptor gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12930811 10766 Igf1r insulin-like growth factor I receptor gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:12930811 10766 Igf1r insulin-like growth factor I receptor gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20160714 MGI PMID:25238791 10766 Igf1r insulin-like growth factor I receptor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20160714 MGI PMID:25238791 10766 Igf1r insulin-like growth factor I receptor gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0001238 thin epidermis stratum spinosum IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:18443199 10766 Igf1r insulin-like growth factor I receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18443199 10766 Igf1r insulin-like growth factor I receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20170720 MGI PMID:27861515 10766 Igf1r insulin-like growth factor I receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10875258 10766 Igf1r insulin-like growth factor I receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160714 MGI PMID:25238791 10766 Igf1r insulin-like growth factor I receptor gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:8806828 10766 Igf1r insulin-like growth factor I receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:12215457 10766 Igf1r insulin-like growth factor I receptor gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:12215457 10766 Igf1r insulin-like growth factor I receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17416680 10766 Igf1r insulin-like growth factor I receptor gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10875258 10766 Igf1r insulin-like growth factor I receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160714 MGI PMID:25238791 10766 Igf1r insulin-like growth factor I receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8806828 10766 Igf1r insulin-like growth factor I receptor gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10875258 10766 Igf1r insulin-like growth factor I receptor gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18443199 10766 Igf1r insulin-like growth factor I receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10875258 10766 Igf1r insulin-like growth factor I receptor gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:11818962 10766 Igf1r insulin-like growth factor I receptor gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:14628051 10766 Igf1r insulin-like growth factor I receptor gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20170803 MGI PMID:28207927 10766 Igf1r insulin-like growth factor I receptor gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20160714 MGI PMID:25238791 10766 Igf1r insulin-like growth factor I receptor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:18443199 10766 Igf1r insulin-like growth factor I receptor gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:18443199 10766 Igf1r insulin-like growth factor I receptor gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:18443199 10766 Igf1r insulin-like growth factor I receptor gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:14628051 10766 Igf1r insulin-like growth factor I receptor gene MP:0002996 ovotestis IAGP N RGD:5509061 20141003 MGI PMID:14628051 10766 Igf1r insulin-like growth factor I receptor gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20160714 MGI PMID:25238791 10766 Igf1r insulin-like growth factor I receptor gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22733797 10766 Igf1r insulin-like growth factor I receptor gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:8806828 10766 Igf1r insulin-like growth factor I receptor gene MP:0004260 enlarged placenta IAGP N RGD:5509061 20141003 MGI PMID:8806828 10766 Igf1r insulin-like growth factor I receptor gene MP:0004289 abnormal bony labyrinth IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0004408 decreased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0004589 abnormal cochlear hair cell development IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20160714 MGI PMID:25238791 10766 Igf1r insulin-like growth factor I receptor gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:22733797 10766 Igf1r insulin-like growth factor I receptor gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:18443199 10766 Igf1r insulin-like growth factor I receptor gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:12215457 10766 Igf1r insulin-like growth factor I receptor gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:12215457 10766 Igf1r insulin-like growth factor I receptor gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:12215457 10766 Igf1r insulin-like growth factor I receptor gene MP:0005159 azoospermia IAGP N RGD:5509061 20160714 MGI PMID:25238791 10766 Igf1r insulin-like growth factor I receptor gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20170720 MGI PMID:27861515 10766 Igf1r insulin-like growth factor I receptor gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20170720 MGI PMID:28655914 10766 Igf1r insulin-like growth factor I receptor gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17416680 10766 Igf1r insulin-like growth factor I receptor gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18443199 10766 Igf1r insulin-like growth factor I receptor gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12215457 10766 Igf1r insulin-like growth factor I receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18443199 10766 Igf1r insulin-like growth factor I receptor gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20170803 MGI PMID:28207927 10766 Igf1r insulin-like growth factor I receptor gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:18443199 10766 Igf1r insulin-like growth factor I receptor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:8806828 10766 Igf1r insulin-like growth factor I receptor gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:8806828 10766 Igf1r insulin-like growth factor I receptor gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18443199 10766 Igf1r insulin-like growth factor I receptor gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12215457 10766 Igf1r insulin-like growth factor I receptor gene MP:0009673 increased birth weight IAGP N RGD:5509061 20141003 MGI PMID:8806828 10766 Igf1r insulin-like growth factor I receptor gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:8806828 10766 Igf1r insulin-like growth factor I receptor gene MP:0009728 abnormal calcaneum morphology IAGP N RGD:5509061 20141003 MGI PMID:11846487 10766 Igf1r insulin-like growth factor I receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18443199 10766 Igf1r insulin-like growth factor I receptor gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19174523 10766 Igf1r insulin-like growth factor I receptor gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0010862 decreased respiratory mucosa goblet cell number IAGP N RGD:5509061 20170803 MGI PMID:28207927 10766 Igf1r insulin-like growth factor I receptor gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:12215457 10766 Igf1r insulin-like growth factor I receptor gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:12215457 10766 Igf1r insulin-like growth factor I receptor gene MP:0010897 abnormal bronchiole epithelium morphology IAGP N RGD:5509061 20160714 MGI PMID:25238791 10766 Igf1r insulin-like growth factor I receptor gene MP:0010897 abnormal bronchiole epithelium morphology IAGP N RGD:5509061 20170720 MGI PMID:27861515 10766 Igf1r insulin-like growth factor I receptor gene MP:0010901 abnormal pulmonary alveolar parenchyma morphology IAGP N RGD:5509061 20160714 MGI PMID:25238791 10766 Igf1r insulin-like growth factor I receptor gene MP:0011061 abnormal inner hair cell kinocilium morphology IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17189427 10766 Igf1r insulin-like growth factor I receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8806824 10766 Igf1r insulin-like growth factor I receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8806828 10766 Igf1r insulin-like growth factor I receptor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10875258 10766 Igf1r insulin-like growth factor I receptor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22159122 10766 Igf1r insulin-like growth factor I receptor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8402901 10766 Igf1r insulin-like growth factor I receptor gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11846487 10766 Igf1r insulin-like growth factor I receptor gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8806828 10766 Igf1r insulin-like growth factor I receptor gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:19174523 10766 Igf1r insulin-like growth factor I receptor gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:12215457 10766 Igf1r insulin-like growth factor I receptor gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:12215457 10766 Igf1r insulin-like growth factor I receptor gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20170803 MGI PMID:28207927 10766 Igf1r insulin-like growth factor I receptor gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20170720 MGI PMID:28655914 10766 Igf1r insulin-like growth factor I receptor gene MP:0030279 thin neurocranium IAGP N RGD:5509061 20171102 MGI PMID:12215457 10766 Igf1r insulin-like growth factor I receptor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:17189427 10766453 Char11_m P. chabaudi malaria resistance QTL 11 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20160211 MGI PMID:9398835 10766453 Char11_m P. chabaudi malaria resistance QTL 11 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:9398835 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0000691 enlarged spleen IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0001829 increased activated T cell number IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0001859 kidney inflammation IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0002083 premature death IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0002871 albuminuria IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20160211 MGI PMID:16943797 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20160211 MGI PMID:16943797 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20160211 MGI PMID:16943797 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20160211 MGI PMID:16943797 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20160211 MGI PMID:16943797 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0005014 increased B cell number IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:16943797 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:16943797 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16943797 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:16943797 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:16943797 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:16943797 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:16943797 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0008500 increased IgG2a level IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:16943797 10766456 Sle21_m systematic lupus erythematosus susceptibility 21 (mouse) qtl MP:0011508 abnormal glomerular capillary thrombosis IAGP N RGD:5509061 20160211 MGI PMID:21724994 10766458 Nba12_m New Zealand Black autoimmunity 12 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20160211 MGI PMID:12215897 10766458 Nba12_m New Zealand Black autoimmunity 12 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:12215897 10770 Igf2 insulin-like growth factor 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:8402901 10770 Igf2 insulin-like growth factor 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8402901 10770 Igf2 insulin-like growth factor 2 gene MP:0001238 thin epidermis stratum spinosum IAGP N RGD:5509061 20141003 MGI PMID:8402901 10770 Igf2 insulin-like growth factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11846487 10770 Igf2 insulin-like growth factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:1997210 10770 Igf2 insulin-like growth factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:2330056 10770 Igf2 insulin-like growth factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7536897 10770 Igf2 insulin-like growth factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8402901 10770 Igf2 insulin-like growth factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11743023 10770 Igf2 insulin-like growth factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8806828 10770 Igf2 insulin-like growth factor 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:8806828 10770 Igf2 insulin-like growth factor 2 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:11017078 10770 Igf2 insulin-like growth factor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:8402901 10770 Igf2 insulin-like growth factor 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:11017078 10770 Igf2 insulin-like growth factor 2 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:11743023 10770 Igf2 insulin-like growth factor 2 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:11846487 10770 Igf2 insulin-like growth factor 2 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:15150410 10770 Igf2 insulin-like growth factor 2 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:1997210 10770 Igf2 insulin-like growth factor 2 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:8402901 10770 Igf2 insulin-like growth factor 2 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:8402901 10770 Igf2 insulin-like growth factor 2 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:11432838 10770 Igf2 insulin-like growth factor 2 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0003956 abnormal body size IAGP N RGD:5509061 20141003 MGI PMID:11846487 10770 Igf2 insulin-like growth factor 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12087403 10770 Igf2 insulin-like growth factor 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0004196 abnormal prenatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:12087403 10770 Igf2 insulin-like growth factor 2 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:12087403 10770 Igf2 insulin-like growth factor 2 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:15150410 10770 Igf2 insulin-like growth factor 2 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:8806828 10770 Igf2 insulin-like growth factor 2 gene MP:0004265 abnormal placental transport IAGP N RGD:5509061 20141003 MGI PMID:12087403 10770 Igf2 insulin-like growth factor 2 gene MP:0004265 abnormal placental transport IAGP N RGD:5509061 20141003 MGI PMID:15150410 10770 Igf2 insulin-like growth factor 2 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:12032310 10770 Igf2 insulin-like growth factor 2 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:15150410 10770 Igf2 insulin-like growth factor 2 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0009265 delayed eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:12032310 10770 Igf2 insulin-like growth factor 2 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:15150410 10770 Igf2 insulin-like growth factor 2 gene MP:0009432 increased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0009673 increased birth weight IAGP N RGD:5509061 20141003 MGI PMID:8806828 10770 Igf2 insulin-like growth factor 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:8402901 10770 Igf2 insulin-like growth factor 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:8806828 10770 Igf2 insulin-like growth factor 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:11017078 10770 Igf2 insulin-like growth factor 2 gene MP:0010591 enlarged aortic valve IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0010600 enlarged pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0010865 prenatal growth retardation IEA N RGD:5509061 20141003 MGI 10770 Igf2 insulin-like growth factor 2 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0010970 abnormal compact bone lamellar structure IAGP N RGD:5509061 20141003 MGI PMID:21148188 10770 Igf2 insulin-like growth factor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8806828 10770 Igf2 insulin-like growth factor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8402901 10770 Igf2 insulin-like growth factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9389646 10770 Igf2 insulin-like growth factor 2 gene MP:0012098 increased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:12032310 10770 Igf2 insulin-like growth factor 2 gene MP:0013309 adrenal gland cyst IAGP N RGD:5509061 20141120 MGI PMID:9389646 10771 Igfbp2 insulin-like growth factor binding protein 2 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:10976924 10771 Igfbp2 insulin-like growth factor binding protein 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 10771 Igfbp2 insulin-like growth factor binding protein 2 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:10976924 10771 Igfbp2 insulin-like growth factor binding protein 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:10976924 10771 Igfbp2 insulin-like growth factor binding protein 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:10976924 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16675541 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20926583 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16675541 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:20926583 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20926583 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160421 MGI 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16675541 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20926583 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16675541 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20926583 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20926583 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20200109 MGI PMID:31526985 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20211021 MGI 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20926583 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:16675541 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200109 MGI PMID:31526985 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0003900 shortened QT interval IEA N RGD:5509061 20230601 MGI 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:16675541 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:20926583 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16675541 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20926583 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16675541 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16675541 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20200109 MGI PMID:31526985 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16675541 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0008961 abnormal basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:20926583 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0009427 increased tibialis anterior weight IAGP N RGD:5509061 20141003 MGI PMID:20926583 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0010226 increased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:20926583 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:16675541 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0010571 shortened ST segment IEA N RGD:5509061 20201022 MGI 10774 Igfbp3 insulin-like growth factor binding protein 3 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200109 MGI PMID:31526985 10775 Igfbp4 insulin-like growth factor binding protein 4 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16675541 10775 Igfbp4 insulin-like growth factor binding protein 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16675541 10775 Igfbp4 insulin-like growth factor binding protein 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16675541 10775 Igfbp4 insulin-like growth factor binding protein 4 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16675541 10775 Igfbp4 insulin-like growth factor binding protein 4 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:16675541 10775 Igfbp4 insulin-like growth factor binding protein 4 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:16675541 10775 Igfbp4 insulin-like growth factor binding protein 4 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16675541 10775 Igfbp4 insulin-like growth factor binding protein 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16675541 10775 Igfbp4 insulin-like growth factor binding protein 4 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16675541 10775 Igfbp4 insulin-like growth factor binding protein 4 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16675541 10775 Igfbp4 insulin-like growth factor binding protein 4 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16675541 10775 Igfbp4 insulin-like growth factor binding protein 4 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:16675541 10775 Igfbp4 insulin-like growth factor binding protein 4 gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:16675541 10776 Igfbp5 insulin-like growth factor binding protein 5 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16675541 10776 Igfbp5 insulin-like growth factor binding protein 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16675541 10776 Igfbp5 insulin-like growth factor binding protein 5 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16675541 10776 Igfbp5 insulin-like growth factor binding protein 5 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16675541 10776 Igfbp5 insulin-like growth factor binding protein 5 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:16675541 10776 Igfbp5 insulin-like growth factor binding protein 5 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:16675541 10776 Igfbp5 insulin-like growth factor binding protein 5 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16675541 10776 Igfbp5 insulin-like growth factor binding protein 5 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16675541 10776 Igfbp5 insulin-like growth factor binding protein 5 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16675541 10776 Igfbp5 insulin-like growth factor binding protein 5 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16675541 10776 Igfbp5 insulin-like growth factor binding protein 5 gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:16675541 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20111116 MGI PMID:18925577 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20111116 MGI PMID:20458139 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20111116 MGI PMID:9103198 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:20512127 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0002495 increased IgA level IAGP N RGD:5509061 20111116 MGI PMID:20512127 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0002497 increased IgE level IAGP N RGD:5509061 20111116 MGI PMID:18925577 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0002606 increased basophil cell number IAGP N RGD:5509061 20111116 MGI PMID:20512127 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:20512127 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:20512127 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20111116 MGI PMID:20512127 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20111116 MGI PMID:18925577 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20111116 MGI PMID:20458139 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20111116 MGI PMID:9103198 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20111116 MGI PMID:18354212 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0008728 increased memory B cell number IAGP N RGD:5509061 20111116 MGI PMID:18925577 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0010215 abnormal circulating complement protein level IAGP N RGD:5509061 20111116 MGI PMID:20512127 10780 Igh-7 immunoglobulin heavy chain 7 (heavy chain of IgE) gene MP:0014471 enhanced B cell migration IAGP N RGD:5509061 20240613 MGI PMID:18925577 10783 Igkc immunoglobulin kappa constant gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20111116 MGI PMID:16785310 10783 Igkc immunoglobulin kappa constant gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20111116 MGI PMID:12538695 10783 Igkc immunoglobulin kappa constant gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20111116 MGI PMID:8458339 10783 Igkc immunoglobulin kappa constant gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20111116 MGI PMID:7664778 10783 Igkc immunoglobulin kappa constant gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20111116 MGI PMID:7664778 10783 Igkc immunoglobulin kappa constant gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20111116 MGI PMID:12538695 10783 Igkc immunoglobulin kappa constant gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20111116 MGI PMID:8075633 10783 Igkc immunoglobulin kappa constant gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20111116 MGI PMID:9687526 10783 Igkc immunoglobulin kappa constant gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20111116 MGI PMID:18086860 10783 Igkc immunoglobulin kappa constant gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20111116 MGI PMID:18086860 10783 Igkc immunoglobulin kappa constant gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20111116 MGI PMID:18086860 10783 Igkc immunoglobulin kappa constant gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20111116 MGI PMID:8235658 10783 Igkc immunoglobulin kappa constant gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20111116 MGI PMID:8458339 10783 Igkc immunoglobulin kappa constant gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20111116 MGI PMID:9687526 10783 Igkc immunoglobulin kappa constant gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20111116 MGI PMID:7664778 10783 Igkc immunoglobulin kappa constant gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20111116 MGI PMID:18086860 10783 Igkc immunoglobulin kappa constant gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20111116 MGI PMID:12538695 10783 Igkc immunoglobulin kappa constant gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20111116 MGI PMID:7664778 10783 Igkc immunoglobulin kappa constant gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20130503 MGI PMID:23296705 10783 Igkc immunoglobulin kappa constant gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20111116 MGI PMID:8075633 10783 Igkc immunoglobulin kappa constant gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20111116 MGI PMID:9020839 10783 Igkc immunoglobulin kappa constant gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20111116 MGI PMID:9687526 10783 Igkc immunoglobulin kappa constant gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20130503 MGI PMID:23296705 10783 Igkc immunoglobulin kappa constant gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20111116 MGI PMID:9687526 10783 Igkc immunoglobulin kappa constant gene MP:0003134 increased late pro-B cell number IAGP N RGD:5509061 20111116 MGI PMID:9687526 10783 Igkc immunoglobulin kappa constant gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20111116 MGI PMID:8075633 10783 Igkc immunoglobulin kappa constant gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20111116 MGI PMID:9020839 10783 Igkc immunoglobulin kappa constant gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20111116 MGI PMID:9687526 10783 Igkc immunoglobulin kappa constant gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20111116 MGI PMID:12538695 10783 Igkc immunoglobulin kappa constant gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20111116 MGI PMID:16785310 10783 Igkc immunoglobulin kappa constant gene MP:0005022 abnormal immature B cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12538695 10783 Igkc immunoglobulin kappa constant gene MP:0008071 absent B cells IAGP N RGD:5509061 20111116 MGI PMID:12538695 10783 Igkc immunoglobulin kappa constant gene MP:0008071 absent B cells IAGP N RGD:5509061 20111116 MGI PMID:8075633 10783 Igkc immunoglobulin kappa constant gene MP:0008202 absent B-1 B cells IAGP N RGD:5509061 20111116 MGI PMID:12538695 10783 Igkc immunoglobulin kappa constant gene MP:0008205 absent B-2 B cells IAGP N RGD:5509061 20111116 MGI PMID:12538695 10783 Igkc immunoglobulin kappa constant gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20111116 MGI PMID:9687526 10783 Igkc immunoglobulin kappa constant gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20111116 MGI PMID:8075633 10783 Igkc immunoglobulin kappa constant gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20111116 MGI PMID:8458339 10783 Igkc immunoglobulin kappa constant gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20111116 MGI PMID:9020839 10783 Igkc immunoglobulin kappa constant gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20111116 MGI PMID:8458339 10783 Igkc immunoglobulin kappa constant gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20111116 MGI PMID:9687526 10783 Igkc immunoglobulin kappa constant gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20111116 MGI PMID:12538695 10783 Igkc immunoglobulin kappa constant gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20111116 MGI PMID:9020839 10783 Igkc immunoglobulin kappa constant gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20111116 MGI PMID:9687526 10783 Igkc immunoglobulin kappa constant gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20111116 MGI PMID:8458339 10783 Igkc immunoglobulin kappa constant gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20111116 MGI PMID:9687526 10783 Igkc immunoglobulin kappa constant gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20111116 MGI PMID:18086860 10783 Igkc immunoglobulin kappa constant gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20111116 MGI PMID:9020839 10783 Igkc immunoglobulin kappa constant gene MP:0008761 abnormal immunoglobulin light chain V-J recombination IAGP N RGD:5509061 20111116 MGI PMID:19116268 10783 Igkc immunoglobulin kappa constant gene MP:0008761 abnormal immunoglobulin light chain V-J recombination IAGP N RGD:5509061 20111116 MGI PMID:9020839 10783 Igkc immunoglobulin kappa constant gene MP:0008761 abnormal immunoglobulin light chain V-J recombination IAGP N RGD:5509061 20111116 MGI PMID:9687526 10784 Igl immunoglobulin lambda chain complex gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12538695 10784 Igl immunoglobulin lambda chain complex gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12538695 10784 Igl immunoglobulin lambda chain complex gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:18086860 10784 Igl immunoglobulin lambda chain complex gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:18086860 10784 Igl immunoglobulin lambda chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18086860 10784 Igl immunoglobulin lambda chain complex gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18086860 10784 Igl immunoglobulin lambda chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12538695 10784 Igl immunoglobulin lambda chain complex gene MP:0005022 abnormal immature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12538695 10784 Igl immunoglobulin lambda chain complex gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:12538695 10784 Igl immunoglobulin lambda chain complex gene MP:0008202 absent B-1 B cells IAGP N RGD:5509061 20141003 MGI PMID:12538695 10784 Igl immunoglobulin lambda chain complex gene MP:0008205 absent B-2 B cells IAGP N RGD:5509061 20141003 MGI PMID:12538695 10784 Igl immunoglobulin lambda chain complex gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:12538695 10784 Igl immunoglobulin lambda chain complex gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:18086860 10785 Il10 interleukin 10 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15362035 10785 Il10 interleukin 10 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12765335 10785 Il10 interleukin 10 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12765335 10785 Il10 interleukin 10 gene MP:0000199 abnormal circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:15362035 10785 Il10 interleukin 10 gene MP:0000216 absent erythroid progenitor cell IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:8770874 10785 Il10 interleukin 10 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:8770874 10785 Il10 interleukin 10 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20141003 MGI PMID:15534372 10785 Il10 interleukin 10 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:15534372 10785 Il10 interleukin 10 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:17617560 10785 Il10 interleukin 10 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:24442434 10785 Il10 interleukin 10 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20160324 MGI PMID:25172014 10785 Il10 interleukin 10 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:11285204 10785 Il10 interleukin 10 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:15534372 10785 Il10 interleukin 10 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:15534372 10785 Il10 interleukin 10 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:16709607 10785 Il10 interleukin 10 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19620304 10785 Il10 interleukin 10 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8770874 10785 Il10 interleukin 10 gene MP:0000745 tremors IEA N RGD:5509061 20170126 MGI 10785 Il10 interleukin 10 gene MP:0000880 decreased Purkinje cell number IEA N RGD:5509061 20170126 MGI 10785 Il10 interleukin 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10579119 10785 Il10 interleukin 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12823276 10785 Il10 interleukin 10 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10859330 10785 Il10 interleukin 10 gene MP:0001393 ataxia IEA N RGD:5509061 20170126 MGI 10785 Il10 interleukin 10 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18650318 10785 Il10 interleukin 10 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:11353686 10785 Il10 interleukin 10 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:15362035 10785 Il10 interleukin 10 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:16709607 10785 Il10 interleukin 10 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:16497487 10785 Il10 interleukin 10 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:18375937 10785 Il10 interleukin 10 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16709607 10785 Il10 interleukin 10 gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:10859330 10785 Il10 interleukin 10 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:8770874 10785 Il10 interleukin 10 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17111348 10785 Il10 interleukin 10 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:15534372 10785 Il10 interleukin 10 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:17003481 10785 Il10 interleukin 10 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:17015721 10785 Il10 interleukin 10 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:8770874 10785 Il10 interleukin 10 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15534372 10785 Il10 interleukin 10 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18387831 10785 Il10 interleukin 10 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:18026113 10785 Il10 interleukin 10 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:12799032 10785 Il10 interleukin 10 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17579057 10785 Il10 interleukin 10 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16709607 10785 Il10 interleukin 10 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0002083 premature death IAGP N RGD:5509061 20160324 MGI PMID:25172014 10785 Il10 interleukin 10 gene MP:0002148 abnormal hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:15534372 10785 Il10 interleukin 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15534372 10785 Il10 interleukin 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17137799 10785 Il10 interleukin 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19620304 10785 Il10 interleukin 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21844394 10785 Il10 interleukin 10 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:10811896 10785 Il10 interleukin 10 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:15618456 10785 Il10 interleukin 10 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:15534372 10785 Il10 interleukin 10 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15534372 10785 Il10 interleukin 10 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:15534372 10785 Il10 interleukin 10 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18832734 10785 Il10 interleukin 10 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:10811896 10785 Il10 interleukin 10 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0002534 abnormal type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18387831 10785 Il10 interleukin 10 gene MP:0002534 abnormal type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:8823360 10785 Il10 interleukin 10 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:12765335 10785 Il10 interleukin 10 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:17200193 10785 Il10 interleukin 10 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16709607 10785 Il10 interleukin 10 gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:10579119 10785 Il10 interleukin 10 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:11285204 10785 Il10 interleukin 10 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:12823276 10785 Il10 interleukin 10 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:18375937 10785 Il10 interleukin 10 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:18387831 10785 Il10 interleukin 10 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:24442434 10785 Il10 interleukin 10 gene MP:0002816 colitis IAGP N RGD:5509061 20160324 MGI PMID:25172014 10785 Il10 interleukin 10 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16709607 10785 Il10 interleukin 10 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:15362035 10785 Il10 interleukin 10 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11285204 10785 Il10 interleukin 10 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15534372 10785 Il10 interleukin 10 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17111348 10785 Il10 interleukin 10 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:19074677 10785 Il10 interleukin 10 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:10512928 10785 Il10 interleukin 10 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:11406467 10785 Il10 interleukin 10 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:15362035 10785 Il10 interleukin 10 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:15534372 10785 Il10 interleukin 10 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:17617560 10785 Il10 interleukin 10 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:8770874 10785 Il10 interleukin 10 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:8770874 10785 Il10 interleukin 10 gene MP:0003434 decreased susceptibility to induced choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:16903779 10785 Il10 interleukin 10 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:15362035 10785 Il10 interleukin 10 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16497487 10785 Il10 interleukin 10 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15618456 10785 Il10 interleukin 10 gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19620304 10785 Il10 interleukin 10 gene MP:0004504 decreased incidence of tumors by UV induction IAGP N RGD:5509061 20141003 MGI PMID:17579057 10785 Il10 interleukin 10 gene MP:0004752 decreased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:9366559 10785 Il10 interleukin 10 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:18832734 10785 Il10 interleukin 10 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:10947805 10785 Il10 interleukin 10 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19074677 10785 Il10 interleukin 10 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12391195 10785 Il10 interleukin 10 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18387831 10785 Il10 interleukin 10 gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:15362035 10785 Il10 interleukin 10 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19620304 10785 Il10 interleukin 10 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19620304 10785 Il10 interleukin 10 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15534372 10785 Il10 interleukin 10 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17600128 10785 Il10 interleukin 10 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:19941312 10785 Il10 interleukin 10 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:24442434 10785 Il10 interleukin 10 gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0005046 absent spleen white pulp IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17579057 10785 Il10 interleukin 10 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12765335 10785 Il10 interleukin 10 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16709607 10785 Il10 interleukin 10 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16709607 10785 Il10 interleukin 10 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16709607 10785 Il10 interleukin 10 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12765335 10785 Il10 interleukin 10 gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9886396 10785 Il10 interleukin 10 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:16497487 10785 Il10 interleukin 10 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:18375937 10785 Il10 interleukin 10 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:18375937 10785 Il10 interleukin 10 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15362035 10785 Il10 interleukin 10 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:15362035 10785 Il10 interleukin 10 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:9886396 10785 Il10 interleukin 10 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:10947805 10785 Il10 interleukin 10 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19620304 10785 Il10 interleukin 10 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8770874 10785 Il10 interleukin 10 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16778988 10785 Il10 interleukin 10 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16778988 10785 Il10 interleukin 10 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:19620304 10785 Il10 interleukin 10 gene MP:0008121 increased myeloid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:19620304 10785 Il10 interleukin 10 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:10947805 10785 Il10 interleukin 10 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8770874 10785 Il10 interleukin 10 gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19620304 10785 Il10 interleukin 10 gene MP:0008387 hypochromic anemia IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:15362035 10785 Il10 interleukin 10 gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20141003 MGI PMID:16709607 10785 Il10 interleukin 10 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17574631 10785 Il10 interleukin 10 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:10811896 10785 Il10 interleukin 10 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:10811896 10785 Il10 interleukin 10 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:19941312 10785 Il10 interleukin 10 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:18375937 10785 Il10 interleukin 10 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16380512 10785 Il10 interleukin 10 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19941312 10785 Il10 interleukin 10 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 10785 Il10 interleukin 10 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16778988 10785 Il10 interleukin 10 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18375937 10785 Il10 interleukin 10 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:12765335 10785 Il10 interleukin 10 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:19941312 10785 Il10 interleukin 10 gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:19620304 10785 Il10 interleukin 10 gene MP:0008595 abnormal circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:23241891 10785 Il10 interleukin 10 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18650318 10785 Il10 interleukin 10 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:19941312 10785 Il10 interleukin 10 gene MP:0008599 increased circulating interleukin-2 level IAGP N RGD:5509061 20141003 MGI PMID:19941312 10785 Il10 interleukin 10 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:19941312 10785 Il10 interleukin 10 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:12765335 10785 Il10 interleukin 10 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:16380512 10785 Il10 interleukin 10 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:19941312 10785 Il10 interleukin 10 gene MP:0008638 increased circulating interleukin-1 alpha level IAGP N RGD:5509061 20141003 MGI PMID:19941312 10785 Il10 interleukin 10 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:18650318 10785 Il10 interleukin 10 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:19941312 10785 Il10 interleukin 10 gene MP:0008646 abnormal circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:23241891 10785 Il10 interleukin 10 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:18387831 10785 Il10 interleukin 10 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 10785 Il10 interleukin 10 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21460847 10785 Il10 interleukin 10 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:24442434 10785 Il10 interleukin 10 gene MP:0008666 increased interleukin-12a secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 10785 Il10 interleukin 10 gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 10785 Il10 interleukin 10 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:16778988 10785 Il10 interleukin 10 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:18375937 10785 Il10 interleukin 10 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 10785 Il10 interleukin 10 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18650318 10785 Il10 interleukin 10 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:19941312 10785 Il10 interleukin 10 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:8770874 10785 Il10 interleukin 10 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:19941312 10785 Il10 interleukin 10 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16380512 10785 Il10 interleukin 10 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17111348 10785 Il10 interleukin 10 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:19620304 10785 Il10 interleukin 10 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:17579057 10785 Il10 interleukin 10 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:8770874 10785 Il10 interleukin 10 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:8770874 10785 Il10 interleukin 10 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:9886396 10785 Il10 interleukin 10 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:9886396 10785 Il10 interleukin 10 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12842419 10785 Il10 interleukin 10 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:8402911 10785 Il10 interleukin 10 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15618456 10785 Il10 interleukin 10 gene MP:0009310 increased large intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8770874 10785 Il10 interleukin 10 gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17617560 10785 Il10 interleukin 10 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:15362035 10785 Il10 interleukin 10 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16709607 10785 Il10 interleukin 10 gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20141003 MGI PMID:19941312 10785 Il10 interleukin 10 gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20141003 MGI PMID:8770874 10785 Il10 interleukin 10 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:16476050 10785 Il10 interleukin 10 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15534372 10785 Il10 interleukin 10 gene MP:0009816 increased leukotriene level IAGP N RGD:5509061 20141003 MGI PMID:10811896 10785 Il10 interleukin 10 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:15362035 10785 Il10 interleukin 10 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:10579119 10785 Il10 interleukin 10 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:12765335 10785 Il10 interleukin 10 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20160324 MGI PMID:25172014 10785 Il10 interleukin 10 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:15362035 10785 Il10 interleukin 10 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:15362035 10785 Il10 interleukin 10 gene MP:0010962 decreased compact bone mass IAGP N RGD:5509061 20141003 MGI PMID:15362035 10785 Il10 interleukin 10 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:11353686 10785 Il10 interleukin 10 gene MP:0011520 increased placental labyrinth size IAGP N RGD:5509061 20141003 MGI PMID:12842419 10785 Il10 interleukin 10 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:18650318 10785 Il10 interleukin 10 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:24442434 10785 Il10 interleukin 10 gene MP:0030466 alveolar process atrophy IAGP N RGD:5509061 20171221 MGI PMID:17305866 10785 Il10 interleukin 10 gene MP:0031157 abnormal arterial thrombosis IAGP N RGD:5509061 20201210 MGI PMID:12765335 10786 Il15 interleukin 15 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20180111 MGI PMID:21964024 10786 Il15 interleukin 15 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200402 MGI 10786 Il15 interleukin 15 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:10704459 10786 Il15 interleukin 15 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12816981 10786 Il15 interleukin 15 gene MP:0001513 limb grasping IEA N RGD:5509061 20160421 MGI 10786 Il15 interleukin 15 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:10704459 10786 Il15 interleukin 15 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:10704459 10786 Il15 interleukin 15 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15845528 10786 Il15 interleukin 15 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15845528 10786 Il15 interleukin 15 gene MP:0002083 premature death IAGP N RGD:5509061 20180111 MGI PMID:21964024 10786 Il15 interleukin 15 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10704459 10786 Il15 interleukin 15 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16020505 10786 Il15 interleukin 15 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15845528 10786 Il15 interleukin 15 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10704459 10786 Il15 interleukin 15 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15845528 10786 Il15 interleukin 15 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:12816981 10786 Il15 interleukin 15 gene MP:0003995 abnormal uterine artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12816981 10786 Il15 interleukin 15 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15630141 10786 Il15 interleukin 15 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20180111 MGI PMID:21964024 10786 Il15 interleukin 15 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20180111 MGI PMID:21964024 10786 Il15 interleukin 15 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23805138 10786 Il15 interleukin 15 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15845528 10786 Il15 interleukin 15 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:15845528 10786 Il15 interleukin 15 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 10786 Il15 interleukin 15 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:14635060 10786 Il15 interleukin 15 gene MP:0008038 abnormal NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:22346732 10786 Il15 interleukin 15 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:22346732 10786 Il15 interleukin 15 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:10704459 10786 Il15 interleukin 15 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:12586624 10786 Il15 interleukin 15 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:16449532 10786 Il15 interleukin 15 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19084435 10786 Il15 interleukin 15 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:22346732 10786 Il15 interleukin 15 gene MP:0008047 absent uterine NK cells IAGP N RGD:5509061 20141003 MGI PMID:12816981 10786 Il15 interleukin 15 gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16449532 10786 Il15 interleukin 15 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20151231 MGI PMID:24516120 10786 Il15 interleukin 15 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10704459 10786 Il15 interleukin 15 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16860759 10786 Il15 interleukin 15 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16880398 10786 Il15 interleukin 15 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23109710 10786 Il15 interleukin 15 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16880398 10786 Il15 interleukin 15 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:15845528 10786 Il15 interleukin 15 gene MP:0008363 decreased CD8-positive, gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:19913445 10786 Il15 interleukin 15 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20180111 MGI PMID:21964024 10786 Il15 interleukin 15 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20180111 MGI PMID:21964024 10786 Il15 interleukin 15 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20180111 MGI PMID:21964024 10786 Il15 interleukin 15 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20180111 MGI PMID:21964024 10786 Il15 interleukin 15 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15845528 10786 Il15 interleukin 15 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22346732 10786 Il15 interleukin 15 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:22346732 10786 Il15 interleukin 15 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:15845528 10786 Il15 interleukin 15 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16880398 10786 Il15 interleukin 15 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20180111 MGI PMID:21964024 10786 Il15 interleukin 15 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12816981 10786 Il15 interleukin 15 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 10786 Il15 interleukin 15 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:21964024 10786 Il15 interleukin 15 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:15767447 10786 Il15 interleukin 15 gene MP:0031034 increased susceptibility to Poxviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:10704459 10787 Il17a interleukin 17A gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23064362 10787 Il17a interleukin 17A gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 10787 Il17a interleukin 17A gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 10787 Il17a interleukin 17A gene MP:0000623 decreased salivation IAGP N RGD:5509061 20161110 MGI PMID:25411202 10787 Il17a interleukin 17A gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 10787 Il17a interleukin 17A gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 10787 Il17a interleukin 17A gene MP:0001194 dermatitis IAGP N RGD:5509061 20181122 MGI PMID:25902485 10787 Il17a interleukin 17A gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:19075395 10787 Il17a interleukin 17A gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12354389 10787 Il17a interleukin 17A gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:18411338 10787 Il17a interleukin 17A gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:23123062 10787 Il17a interleukin 17A gene MP:0001866 nasal inflammation IAGP N RGD:5509061 20141003 MGI PMID:19144317 10787 Il17a interleukin 17A gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20200730 MGI PMID:29980436 10787 Il17a interleukin 17A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23123062 10787 Il17a interleukin 17A gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 10787 Il17a interleukin 17A gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:19144317 10787 Il17a interleukin 17A gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22770884 10787 Il17a interleukin 17A gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12354389 10787 Il17a interleukin 17A gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12354389 10787 Il17a interleukin 17A gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:18411338 10787 Il17a interleukin 17A gene MP:0002742 enlarged submandibular lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19144317 10787 Il17a interleukin 17A gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:23123062 10787 Il17a interleukin 17A gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 10787 Il17a interleukin 17A gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:12721360 10787 Il17a interleukin 17A gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20141003 MGI PMID:19144317 10787 Il17a interleukin 17A gene MP:0003747 mouth mucosal ulcer IAGP N RGD:5509061 20141003 MGI PMID:19144317 10787 Il17a interleukin 17A gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23123062 10787 Il17a interleukin 17A gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:23123062 10787 Il17a interleukin 17A gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:18411338 10787 Il17a interleukin 17A gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:23123062 10787 Il17a interleukin 17A gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 10787 Il17a interleukin 17A gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22770884 10787 Il17a interleukin 17A gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20161110 MGI PMID:25411202 10787 Il17a interleukin 17A gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12354389 10787 Il17a interleukin 17A gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:12354389 10787 Il17a interleukin 17A gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18411338 10787 Il17a interleukin 17A gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 10787 Il17a interleukin 17A gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22770884 10787 Il17a interleukin 17A gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23064362 10787 Il17a interleukin 17A gene MP:0008348 absent gamma-delta T cells IAGP N RGD:5509061 20141003 MGI PMID:22770884 10787 Il17a interleukin 17A gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:23123062 10787 Il17a interleukin 17A gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12354389 10787 Il17a interleukin 17A gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18411338 10787 Il17a interleukin 17A gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:18411338 10787 Il17a interleukin 17A gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:18411338 10787 Il17a interleukin 17A gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:19144317 10787 Il17a interleukin 17A gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19144317 10787 Il17a interleukin 17A gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:19144317 10787 Il17a interleukin 17A gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:19144317 10787 Il17a interleukin 17A gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:18411338 10787 Il17a interleukin 17A gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12354389 10787 Il17a interleukin 17A gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:18411338 10787 Il17a interleukin 17A gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:22770884 10787 Il17a interleukin 17A gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:12354389 10787 Il17a interleukin 17A gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:23123062 10787 Il17a interleukin 17A gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17919941 10787 Il17a interleukin 17A gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23064362 10787 Il17a interleukin 17A gene MP:0009787 increased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20493731 10787 Il17a interleukin 17A gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200723 MGI PMID:29980436 10787 Il17a interleukin 17A gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 10789 Il1a interleukin 1 alpha gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 10789 Il1a interleukin 1 alpha gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23219391 10789 Il1a interleukin 1 alpha gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:12151598 10789 Il1a interleukin 1 alpha gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:12598651 10789 Il1a interleukin 1 alpha gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 10789 Il1a interleukin 1 alpha gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 10789 Il1a interleukin 1 alpha gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23219391 10789 Il1a interleukin 1 alpha gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:9565638 10789 Il1a interleukin 1 alpha gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 10789 Il1a interleukin 1 alpha gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 10789 Il1a interleukin 1 alpha gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20141003 MGI PMID:9565638 10789 Il1a interleukin 1 alpha gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:20937871 10789 Il1a interleukin 1 alpha gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 10789 Il1a interleukin 1 alpha gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:20937871 10789 Il1a interleukin 1 alpha gene MP:0008639 decreased circulating interleukin-1 alpha level IAGP N RGD:5509061 20141003 MGI PMID:9565638 10789 Il1a interleukin 1 alpha gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:9565638 10789 Il1a interleukin 1 alpha gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:9565638 10789 Il1a interleukin 1 alpha gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:9809553 10789 Il1a interleukin 1 alpha gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:12598651 10789 Il1a interleukin 1 alpha gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 10790 Il1b interleukin 1 beta gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20180719 MGI PMID:11549714 10790 Il1b interleukin 1 beta gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20180719 MGI PMID:11549714 10790 Il1b interleukin 1 beta gene MP:0001194 dermatitis IAGP N RGD:5509061 20180719 MGI PMID:12151598 10790 Il1b interleukin 1 beta gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20180719 MGI PMID:10639148 10790 Il1b interleukin 1 beta gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20180719 MGI PMID:12598651 10790 Il1b interleukin 1 beta gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20180719 MGI PMID:7621081 10790 Il1b interleukin 1 beta gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20180719 MGI PMID:18194440 10790 Il1b interleukin 1 beta gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:16861683 10790 Il1b interleukin 1 beta gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20180719 MGI PMID:18493980 10790 Il1b interleukin 1 beta gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20180719 MGI PMID:9565638 10790 Il1b interleukin 1 beta gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20180719 MGI PMID:10639148 10790 Il1b interleukin 1 beta gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20180719 MGI PMID:12598651 10790 Il1b interleukin 1 beta gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20180719 MGI PMID:7621081 10790 Il1b interleukin 1 beta gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20180719 MGI PMID:9565638 10790 Il1b interleukin 1 beta gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20180719 MGI PMID:11265638 10790 Il1b interleukin 1 beta gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180719 MGI PMID:20937871 10790 Il1b interleukin 1 beta gene MP:0004824 decreased susceptibility to experimental autoimmune myasthenia gravis IAGP N RGD:5509061 20180719 MGI PMID:11265638 10790 Il1b interleukin 1 beta gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20180719 MGI PMID:16565512 10790 Il1b interleukin 1 beta gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20180719 MGI PMID:7621081 10790 Il1b interleukin 1 beta gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180719 MGI PMID:11589427 10790 Il1b interleukin 1 beta gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180719 MGI PMID:16439700 10790 Il1b interleukin 1 beta gene MP:0005167 abnormal blood-brain barrier function IAGP N RGD:5509061 20180719 MGI PMID:11589427 10790 Il1b interleukin 1 beta gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20180719 MGI PMID:20937871 10790 Il1b interleukin 1 beta gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20180719 MGI PMID:8666901 10790 Il1b interleukin 1 beta gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20180719 MGI PMID:12598651 10790 Il1b interleukin 1 beta gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:11265638 10790 Il1b interleukin 1 beta gene MP:0008639 decreased circulating interleukin-1 alpha level IAGP N RGD:5509061 20180719 MGI PMID:9565638 10790 Il1b interleukin 1 beta gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20180719 MGI PMID:7621081 10790 Il1b interleukin 1 beta gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20180719 MGI PMID:9565638 10790 Il1b interleukin 1 beta gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20180719 MGI PMID:18493980 10790 Il1b interleukin 1 beta gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20180719 MGI PMID:8666901 10790 Il1b interleukin 1 beta gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20180719 MGI PMID:11265638 10790 Il1b interleukin 1 beta gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20180719 MGI PMID:11265638 10790 Il1b interleukin 1 beta gene MP:0008704 abnormal interleukin-6 secretion IAGP N RGD:5509061 20180719 MGI PMID:7621081 10790 Il1b interleukin 1 beta gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20180719 MGI PMID:9809553 10790 Il1b interleukin 1 beta gene MP:0008831 abnormal insulin-like growth factor I level IAGP N RGD:5509061 20180719 MGI PMID:11549714 10790 Il1b interleukin 1 beta gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180719 MGI PMID:10639148 10790 Il1b interleukin 1 beta gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180719 MGI PMID:11265638 10790 Il1b interleukin 1 beta gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180719 MGI PMID:12598651 10790 Il1b interleukin 1 beta gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20180719 MGI PMID:18493980 10790 Il1b interleukin 1 beta gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20180719 MGI PMID:12598651 10790 Il1b interleukin 1 beta gene MP:0020941 decreased susceptibility to Togaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:9971844 10790 Il1b interleukin 1 beta gene MP:0030524 abnormal tooth root resorption IAGP N RGD:5509061 20180719 MGI PMID:15758271 10790 Il1b interleukin 1 beta gene MP:0031041 decreased susceptibility to Togaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:9971844 10791 Il1rap interleukin 1 receptor accessory protein gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:17908936 10791 Il1rap interleukin 1 receptor accessory protein gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:9820540 10796 Il4 interleukin 4 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20180719 MGI PMID:17913905 10796 Il4 interleukin 4 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180719 MGI PMID:23851689 10796 Il4 interleukin 4 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20180719 MGI PMID:16547221 10796 Il4 interleukin 4 gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20180719 MGI PMID:20512127 10796 Il4 interleukin 4 gene MP:0000466 esophageal epithelium hyperplasia IAGP N RGD:5509061 20180719 MGI PMID:23851689 10796 Il4 interleukin 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180719 MGI PMID:9109438 10796 Il4 interleukin 4 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20180719 MGI PMID:9109438 10796 Il4 interleukin 4 gene MP:0000701 abnormal lymph node size IAGP N RGD:5509061 20180719 MGI PMID:9109438 10796 Il4 interleukin 4 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20180719 MGI PMID:10330435 10796 Il4 interleukin 4 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20180719 MGI PMID:10679097 10796 Il4 interleukin 4 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20180719 MGI PMID:12150887 10796 Il4 interleukin 4 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20180719 MGI PMID:18250447 10796 Il4 interleukin 4 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20180719 MGI PMID:10330435 10796 Il4 interleukin 4 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20180719 MGI PMID:10330435 10796 Il4 interleukin 4 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20180719 MGI PMID:7517363 10796 Il4 interleukin 4 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20180719 MGI PMID:7609051 10796 Il4 interleukin 4 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20180719 MGI PMID:12446913 10796 Il4 interleukin 4 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20180719 MGI PMID:8906833 10796 Il4 interleukin 4 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20180719 MGI PMID:12446913 10796 Il4 interleukin 4 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20180719 MGI PMID:9109438 10796 Il4 interleukin 4 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20180719 MGI PMID:9703318 10796 Il4 interleukin 4 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20180719 MGI PMID:23851689 10796 Il4 interleukin 4 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180719 MGI PMID:11342667 10796 Il4 interleukin 4 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20180719 MGI PMID:23851689 10796 Il4 interleukin 4 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20180719 MGI PMID:16413168 10796 Il4 interleukin 4 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20180719 MGI PMID:10878379 10796 Il4 interleukin 4 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20180719 MGI PMID:10679097 10796 Il4 interleukin 4 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20180719 MGI PMID:20937871 10796 Il4 interleukin 4 gene MP:0001958 emphysema IAGP N RGD:5509061 20180719 MGI PMID:10486156 10796 Il4 interleukin 4 gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:23851689 10796 Il4 interleukin 4 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20180719 MGI PMID:12709397 10796 Il4 interleukin 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:10069422 10796 Il4 interleukin 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:16226507 10796 Il4 interleukin 4 gene MP:0002224 abnormal spleen size IAGP N RGD:5509061 20180719 MGI PMID:9109438 10796 Il4 interleukin 4 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20180719 MGI PMID:21131966 10796 Il4 interleukin 4 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20180719 MGI PMID:12150890 10796 Il4 interleukin 4 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20180719 MGI PMID:17182558 10796 Il4 interleukin 4 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20180719 MGI PMID:9109438 10796 Il4 interleukin 4 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20180719 MGI PMID:12446913 10796 Il4 interleukin 4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:11591797 10796 Il4 interleukin 4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:11745342 10796 Il4 interleukin 4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:12150887 10796 Il4 interleukin 4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:18719110 10796 Il4 interleukin 4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:1948049 10796 Il4 interleukin 4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:20512127 10796 Il4 interleukin 4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:21131966 10796 Il4 interleukin 4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:22138715 10796 Il4 interleukin 4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:22326582 10796 Il4 interleukin 4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:7598937 10796 Il4 interleukin 4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:8384701 10796 Il4 interleukin 4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:8584936 10796 Il4 interleukin 4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:8906833 10796 Il4 interleukin 4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:9109438 10796 Il4 interleukin 4 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20180719 MGI PMID:8384701 10796 Il4 interleukin 4 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20180719 MGI PMID:20512127 10796 Il4 interleukin 4 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20180719 MGI PMID:20512127 10796 Il4 interleukin 4 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20180719 MGI PMID:8906833 10796 Il4 interleukin 4 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20180719 MGI PMID:12150887 10796 Il4 interleukin 4 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20180719 MGI PMID:8906833 10796 Il4 interleukin 4 gene MP:0002606 increased basophil cell number IAGP N RGD:5509061 20180719 MGI PMID:20512127 10796 Il4 interleukin 4 gene MP:0002607 decreased basophil cell number IAGP N RGD:5509061 20180719 MGI PMID:22326582 10796 Il4 interleukin 4 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20180719 MGI PMID:18055812 10796 Il4 interleukin 4 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180719 MGI PMID:11342667 10796 Il4 interleukin 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20180719 MGI PMID:16547221 10796 Il4 interleukin 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20180719 MGI PMID:1948049 10796 Il4 interleukin 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20180719 MGI PMID:9703318 10796 Il4 interleukin 4 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20180719 MGI PMID:7517363 10796 Il4 interleukin 4 gene MP:0003278 esophageal inflammation IAGP N RGD:5509061 20180719 MGI PMID:23851689 10796 Il4 interleukin 4 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20180719 MGI PMID:12150887 10796 Il4 interleukin 4 gene MP:0004031 insulitis IAGP N RGD:5509061 20180719 MGI PMID:9703318 10796 Il4 interleukin 4 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20180719 MGI PMID:20512127 10796 Il4 interleukin 4 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20180719 MGI PMID:20512127 10796 Il4 interleukin 4 gene MP:0004795 decreased anti-nuclear antigen antibody level IAGP N RGD:5509061 20180719 MGI PMID:9109438 10796 Il4 interleukin 4 gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20180719 MGI PMID:9109438 10796 Il4 interleukin 4 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20180719 MGI PMID:9703318 10796 Il4 interleukin 4 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20180719 MGI PMID:9109438 10796 Il4 interleukin 4 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20180719 MGI PMID:12150887 10796 Il4 interleukin 4 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20180719 MGI PMID:23851689 10796 Il4 interleukin 4 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20180719 MGI PMID:22138715 10796 Il4 interleukin 4 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20180719 MGI PMID:7598937 10796 Il4 interleukin 4 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20180719 MGI PMID:23851689 10796 Il4 interleukin 4 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180719 MGI PMID:20512127 10796 Il4 interleukin 4 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20180719 MGI PMID:16547221 10796 Il4 interleukin 4 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20180719 MGI PMID:8384701 10796 Il4 interleukin 4 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20180719 MGI PMID:11745342 10796 Il4 interleukin 4 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20180719 MGI PMID:10330435 10796 Il4 interleukin 4 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20180719 MGI PMID:10679097 10796 Il4 interleukin 4 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20180719 MGI PMID:12150887 10796 Il4 interleukin 4 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20180719 MGI PMID:22138715 10796 Il4 interleukin 4 gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20180719 MGI PMID:7609051 10796 Il4 interleukin 4 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:7517363 10796 Il4 interleukin 4 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180719 MGI PMID:15034018 10796 Il4 interleukin 4 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20180719 MGI PMID:22101429 10796 Il4 interleukin 4 gene MP:0005310 abnormal salivary gland physiology IAGP N RGD:5509061 20180719 MGI PMID:16413168 10796 Il4 interleukin 4 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:7517363 10796 Il4 interleukin 4 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20180719 MGI PMID:15613333 10796 Il4 interleukin 4 gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20180719 MGI PMID:11591797 10796 Il4 interleukin 4 gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20180719 MGI PMID:15613333 10796 Il4 interleukin 4 gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20180719 MGI PMID:17182558 10796 Il4 interleukin 4 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20180719 MGI PMID:10330435 10796 Il4 interleukin 4 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20180719 MGI PMID:12150890 10796 Il4 interleukin 4 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20180719 MGI PMID:16547221 10796 Il4 interleukin 4 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20180719 MGI PMID:19682930 10796 Il4 interleukin 4 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20180719 MGI PMID:8906833 10796 Il4 interleukin 4 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20180719 MGI PMID:20147633 10796 Il4 interleukin 4 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20180719 MGI PMID:9109438 10796 Il4 interleukin 4 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20180719 MGI PMID:15613333 10796 Il4 interleukin 4 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180719 MGI PMID:16413168 10796 Il4 interleukin 4 gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20180719 MGI PMID:17913905 10796 Il4 interleukin 4 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20180719 MGI PMID:17611223 10796 Il4 interleukin 4 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:23851689 10796 Il4 interleukin 4 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20180719 MGI PMID:16778988 10796 Il4 interleukin 4 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20180719 MGI PMID:18719110 10796 Il4 interleukin 4 gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20180719 MGI PMID:17182558 10796 Il4 interleukin 4 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20180719 MGI PMID:7517363 10796 Il4 interleukin 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:11745342 10796 Il4 interleukin 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:12446913 10796 Il4 interleukin 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:1948049 10796 Il4 interleukin 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:20512127 10796 Il4 interleukin 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:21131966 10796 Il4 interleukin 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:22138715 10796 Il4 interleukin 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:22326582 10796 Il4 interleukin 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:8384701 10796 Il4 interleukin 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:8584936 10796 Il4 interleukin 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:8906833 10796 Il4 interleukin 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:9109438 10796 Il4 interleukin 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:9647229 10796 Il4 interleukin 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:9703318 10796 Il4 interleukin 4 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20180719 MGI PMID:12446913 10796 Il4 interleukin 4 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20180719 MGI PMID:12446913 10796 Il4 interleukin 4 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20180719 MGI PMID:12446913 10796 Il4 interleukin 4 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20180719 MGI PMID:9109438 10796 Il4 interleukin 4 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20180719 MGI PMID:11591797 10796 Il4 interleukin 4 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20180719 MGI PMID:20512127 10796 Il4 interleukin 4 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20180719 MGI PMID:9647229 10796 Il4 interleukin 4 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20180719 MGI PMID:20512127 10796 Il4 interleukin 4 gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20180719 MGI PMID:12446913 10796 Il4 interleukin 4 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:10878379 10796 Il4 interleukin 4 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:16778988 10796 Il4 interleukin 4 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:17182558 10796 Il4 interleukin 4 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:8906833 10796 Il4 interleukin 4 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:11591797 10796 Il4 interleukin 4 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20180719 MGI PMID:10878379 10796 Il4 interleukin 4 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20180719 MGI PMID:8384701 10796 Il4 interleukin 4 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20180719 MGI PMID:8906833 10796 Il4 interleukin 4 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20180719 MGI PMID:21131966 10796 Il4 interleukin 4 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20180719 MGI PMID:11591797 10796 Il4 interleukin 4 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20180719 MGI PMID:12150890 10796 Il4 interleukin 4 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20180719 MGI PMID:17182558 10796 Il4 interleukin 4 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20180719 MGI PMID:23851689 10796 Il4 interleukin 4 gene MP:0008697 decreased interleukin-3 secretion IAGP N RGD:5509061 20180719 MGI PMID:8384701 10796 Il4 interleukin 4 gene MP:0008698 abnormal interleukin-4 secretion IAGP N RGD:5509061 20180719 MGI PMID:11591797 10796 Il4 interleukin 4 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20180719 MGI PMID:10486156 10796 Il4 interleukin 4 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20180719 MGI PMID:11163225 10796 Il4 interleukin 4 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20180719 MGI PMID:11323701 10796 Il4 interleukin 4 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20180719 MGI PMID:12150890 10796 Il4 interleukin 4 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20180719 MGI PMID:21131966 10796 Il4 interleukin 4 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20180719 MGI PMID:22326582 10796 Il4 interleukin 4 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20180719 MGI PMID:8384701 10796 Il4 interleukin 4 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20180719 MGI PMID:8906833 10796 Il4 interleukin 4 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20180719 MGI PMID:21131966 10796 Il4 interleukin 4 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20180719 MGI PMID:11591797 10796 Il4 interleukin 4 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20180719 MGI PMID:17182558 10796 Il4 interleukin 4 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20180719 MGI PMID:7598937 10796 Il4 interleukin 4 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20180719 MGI PMID:8384701 10796 Il4 interleukin 4 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20180719 MGI PMID:8906833 10796 Il4 interleukin 4 gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20180719 MGI PMID:18719110 10796 Il4 interleukin 4 gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20180719 MGI PMID:21131966 10796 Il4 interleukin 4 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20180719 MGI PMID:9647229 10796 Il4 interleukin 4 gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20180719 MGI PMID:16413168 10796 Il4 interleukin 4 gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20180719 MGI PMID:18055812 10796 Il4 interleukin 4 gene MP:0008896 increased IgG2c level IAGP N RGD:5509061 20180719 MGI PMID:21131966 10796 Il4 interleukin 4 gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20180719 MGI PMID:10679097 10796 Il4 interleukin 4 gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20180719 MGI PMID:11745342 10796 Il4 interleukin 4 gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20180719 MGI PMID:10679097 10796 Il4 interleukin 4 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20180719 MGI PMID:22101429 10796 Il4 interleukin 4 gene MP:0010215 abnormal circulating complement protein level IAGP N RGD:5509061 20180719 MGI PMID:20512127 10796 Il4 interleukin 4 gene MP:0010750 increased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20180719 MGI PMID:10679097 10796 Il4 interleukin 4 gene MP:0010945 lung epithelium hyperplasia IAGP N RGD:5509061 20180719 MGI PMID:23851689 10796 Il4 interleukin 4 gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20180719 MGI PMID:22101429 10796 Il4 interleukin 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:11342667 10796 Il4 interleukin 4 gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:22101429 10796 Il4 interleukin 4 gene MP:0020912 abnormal susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:7609051 10796 Il4 interleukin 4 gene MP:0030466 alveolar process atrophy IAGP N RGD:5509061 20180719 MGI PMID:17305866 10798 Il4ra interleukin 4 receptor, alpha gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17913905 10798 Il4ra interleukin 4 receptor, alpha gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19770271 10798 Il4ra interleukin 4 receptor, alpha gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18220315 10798 Il4ra interleukin 4 receptor, alpha gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18220315 10798 Il4ra interleukin 4 receptor, alpha gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:11168809 10798 Il4ra interleukin 4 receptor, alpha gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:11168809 10798 Il4ra interleukin 4 receptor, alpha gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15142530 10798 Il4ra interleukin 4 receptor, alpha gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:15142530 10798 Il4ra interleukin 4 receptor, alpha gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:10358179 10798 Il4ra interleukin 4 receptor, alpha gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:18250447 10798 Il4ra interleukin 4 receptor, alpha gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15142530 10798 Il4ra interleukin 4 receptor, alpha gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:14557412 10798 Il4ra interleukin 4 receptor, alpha gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:19770271 10798 Il4ra interleukin 4 receptor, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15142530 10798 Il4ra interleukin 4 receptor, alpha gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:19770271 10798 Il4ra interleukin 4 receptor, alpha gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:14557412 10798 Il4ra interleukin 4 receptor, alpha gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:19770271 10798 Il4ra interleukin 4 receptor, alpha gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:15142530 10798 Il4ra interleukin 4 receptor, alpha gene MP:0002434 abnormal T-helper 2 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14557412 10798 Il4ra interleukin 4 receptor, alpha gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15142530 10798 Il4ra interleukin 4 receptor, alpha gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:9380721 10798 Il4ra interleukin 4 receptor, alpha gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:14557412 10798 Il4ra interleukin 4 receptor, alpha gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:14557412 10798 Il4ra interleukin 4 receptor, alpha gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:19770271 10798 Il4ra interleukin 4 receptor, alpha gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:20392476 10798 Il4ra interleukin 4 receptor, alpha gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:15142530 10798 Il4ra interleukin 4 receptor, alpha gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:14557412 10798 Il4ra interleukin 4 receptor, alpha gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15142530 10798 Il4ra interleukin 4 receptor, alpha gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15142530 10798 Il4ra interleukin 4 receptor, alpha gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15142530 10798 Il4ra interleukin 4 receptor, alpha gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:11168809 10798 Il4ra interleukin 4 receptor, alpha gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15142530 10798 Il4ra interleukin 4 receptor, alpha gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19770271 10798 Il4ra interleukin 4 receptor, alpha gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15142530 10798 Il4ra interleukin 4 receptor, alpha gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15142530 10798 Il4ra interleukin 4 receptor, alpha gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9492006 10798 Il4ra interleukin 4 receptor, alpha gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14557412 10798 Il4ra interleukin 4 receptor, alpha gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22101429 10798 Il4ra interleukin 4 receptor, alpha gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:19770271 10798 Il4ra interleukin 4 receptor, alpha gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:9380721 10798 Il4ra interleukin 4 receptor, alpha gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:19770271 10798 Il4ra interleukin 4 receptor, alpha gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:20392476 10798 Il4ra interleukin 4 receptor, alpha gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23109710 10798 Il4ra interleukin 4 receptor, alpha gene MP:0008091 decreased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:21460847 10798 Il4ra interleukin 4 receptor, alpha gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:11168809 10798 Il4ra interleukin 4 receptor, alpha gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9380721 10798 Il4ra interleukin 4 receptor, alpha gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9380721 10798 Il4ra interleukin 4 receptor, alpha gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9492006 10798 Il4ra interleukin 4 receptor, alpha gene MP:0008551 abnormal circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:18220315 10798 Il4ra interleukin 4 receptor, alpha gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:18220315 10798 Il4ra interleukin 4 receptor, alpha gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:19770271 10798 Il4ra interleukin 4 receptor, alpha gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:9380721 10798 Il4ra interleukin 4 receptor, alpha gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20392476 10798 Il4ra interleukin 4 receptor, alpha gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:9380721 10798 Il4ra interleukin 4 receptor, alpha gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:9380721 10798 Il4ra interleukin 4 receptor, alpha gene MP:0008837 increased transforming growth factor beta level IAGP N RGD:5509061 20141003 MGI PMID:18220315 10798 Il4ra interleukin 4 receptor, alpha gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18220315 10798 Il4ra interleukin 4 receptor, alpha gene MP:0010861 increased respiratory mucosa goblet cell number IAGP N RGD:5509061 20141003 MGI PMID:19770271 10798 Il4ra interleukin 4 receptor, alpha gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:22101429 10798 Il4ra interleukin 4 receptor, alpha gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20141003 MGI PMID:20392476 10799 Il5 interleukin 5 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180719 MGI PMID:8551223 10799 Il5 interleukin 5 gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20180719 MGI PMID:12150887 10799 Il5 interleukin 5 gene MP:0001260 increased body weight IAGP N RGD:5509061 20180719 MGI PMID:11058459 10799 Il5 interleukin 5 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20180719 MGI PMID:22174445 10799 Il5 interleukin 5 gene MP:0001376 abnormal mating receptivity IAGP N RGD:5509061 20180719 MGI PMID:11058459 10799 Il5 interleukin 5 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20180719 MGI PMID:24037376 10799 Il5 interleukin 5 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20180719 MGI PMID:12150887 10799 Il5 interleukin 5 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20180719 MGI PMID:12150887 10799 Il5 interleukin 5 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20180719 MGI PMID:8551223 10799 Il5 interleukin 5 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20180719 MGI PMID:12150887 10799 Il5 interleukin 5 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20180719 MGI PMID:12150887 10799 Il5 interleukin 5 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:12150887 10799 Il5 interleukin 5 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20180719 MGI PMID:12150887 10799 Il5 interleukin 5 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20180719 MGI PMID:16495517 10799 Il5 interleukin 5 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180719 MGI PMID:16495517 10799 Il5 interleukin 5 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20180719 MGI PMID:12150887 10799 Il5 interleukin 5 gene MP:0004260 enlarged placenta IAGP N RGD:5509061 20180719 MGI PMID:11058459 10799 Il5 interleukin 5 gene MP:0004940 abnormal B-1 B cell morphology IAGP N RGD:5509061 20180719 MGI PMID:22174445 10799 Il5 interleukin 5 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20180719 MGI PMID:12150887 10799 Il5 interleukin 5 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20180719 MGI PMID:8574848 10799 Il5 interleukin 5 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20180719 MGI PMID:12150887 10799 Il5 interleukin 5 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:8551223 10799 Il5 interleukin 5 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20180719 MGI PMID:12150887 10799 Il5 interleukin 5 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:16495517 10799 Il5 interleukin 5 gene MP:0008627 decreased circulating interleukin-5 level IAGP N RGD:5509061 20180719 MGI PMID:24037376 10799 Il5 interleukin 5 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20180719 MGI PMID:22174445 10799 Il5 interleukin 5 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20180719 MGI PMID:12150887 10799 Il5 interleukin 5 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20180719 MGI PMID:11058459 10802 Il6 interleukin 6 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17921078 10802 Il6 interleukin 6 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11018077 10802 Il6 interleukin 6 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8131749 10802 Il6 interleukin 6 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:8131749 10802 Il6 interleukin 6 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12223557 10802 Il6 interleukin 6 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12957371 10802 Il6 interleukin 6 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:19234091 10802 Il6 interleukin 6 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:19234091 10802 Il6 interleukin 6 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 10802 Il6 interleukin 6 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:19234091 10802 Il6 interleukin 6 gene MP:0000436 abnormal head movements IAGP N RGD:5509061 20141003 MGI PMID:23085146 10802 Il6 interleukin 6 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:8910279 10802 Il6 interleukin 6 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9169772 10802 Il6 interleukin 6 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10415153 10802 Il6 interleukin 6 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:10415153 10802 Il6 interleukin 6 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12223557 10802 Il6 interleukin 6 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:19918056 10802 Il6 interleukin 6 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:19918056 10802 Il6 interleukin 6 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:11006436 10802 Il6 interleukin 6 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23085146 10802 Il6 interleukin 6 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:14988384 10802 Il6 interleukin 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14988384 10802 Il6 interleukin 6 gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:9875345 10802 Il6 interleukin 6 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:11006436 10802 Il6 interleukin 6 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:9875345 10802 Il6 interleukin 6 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12946594 10802 Il6 interleukin 6 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16843000 10802 Il6 interleukin 6 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19378383 10802 Il6 interleukin 6 gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:11006436 10802 Il6 interleukin 6 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23085146 10802 Il6 interleukin 6 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:19378383 10802 Il6 interleukin 6 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:19436757 10802 Il6 interleukin 6 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15265638 10802 Il6 interleukin 6 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19378383 10802 Il6 interleukin 6 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:15581736 10802 Il6 interleukin 6 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:18367337 10802 Il6 interleukin 6 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:11018077 10802 Il6 interleukin 6 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:8131749 10802 Il6 interleukin 6 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:19234091 10802 Il6 interleukin 6 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15831701 10802 Il6 interleukin 6 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:17615358 10802 Il6 interleukin 6 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:8910279 10802 Il6 interleukin 6 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14988384 10802 Il6 interleukin 6 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:11006436 10802 Il6 interleukin 6 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:20483735 10802 Il6 interleukin 6 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:8666893 10802 Il6 interleukin 6 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12957371 10802 Il6 interleukin 6 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:20483735 10802 Il6 interleukin 6 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:24012418 10802 Il6 interleukin 6 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:9169772 10802 Il6 interleukin 6 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11208530 10802 Il6 interleukin 6 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9284817 10802 Il6 interleukin 6 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:12358740 10802 Il6 interleukin 6 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:10215902 10802 Il6 interleukin 6 gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18056981 10802 Il6 interleukin 6 gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:9284817 10802 Il6 interleukin 6 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:15265638 10802 Il6 interleukin 6 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:19378383 10802 Il6 interleukin 6 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10861297 10802 Il6 interleukin 6 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16581004 10802 Il6 interleukin 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10415153 10802 Il6 interleukin 6 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8127368 10802 Il6 interleukin 6 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12223557 10802 Il6 interleukin 6 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:10415153 10802 Il6 interleukin 6 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:12957371 10802 Il6 interleukin 6 gene MP:0002332 abnormal exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:14988384 10802 Il6 interleukin 6 gene MP:0002336 abnormal pulmonary gas exchange IAGP N RGD:5509061 20141003 MGI PMID:14988384 10802 Il6 interleukin 6 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15831701 10802 Il6 interleukin 6 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:7768607 10802 Il6 interleukin 6 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8127368 10802 Il6 interleukin 6 gene MP:0002433 abnormal T-helper 1 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8666893 10802 Il6 interleukin 6 gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18504307 10802 Il6 interleukin 6 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20083667 10802 Il6 interleukin 6 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:8666893 10802 Il6 interleukin 6 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:7768607 10802 Il6 interleukin 6 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:8666893 10802 Il6 interleukin 6 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:8666893 10802 Il6 interleukin 6 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:16843000 10802 Il6 interleukin 6 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:19378383 10802 Il6 interleukin 6 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:23085146 10802 Il6 interleukin 6 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:16843000 10802 Il6 interleukin 6 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:19378383 10802 Il6 interleukin 6 gene MP:0002711 decreased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:18719127 10802 Il6 interleukin 6 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:10215902 10802 Il6 interleukin 6 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:19234091 10802 Il6 interleukin 6 gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:15265638 10802 Il6 interleukin 6 gene MP:0002801 abnormal long-term object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:19436757 10802 Il6 interleukin 6 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19234091 10802 Il6 interleukin 6 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12223557 10802 Il6 interleukin 6 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:20483735 10802 Il6 interleukin 6 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:8131749 10802 Il6 interleukin 6 gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20141003 MGI PMID:17921078 10802 Il6 interleukin 6 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:18719127 10802 Il6 interleukin 6 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18177723 10802 Il6 interleukin 6 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:17615358 10802 Il6 interleukin 6 gene MP:0003194 abnormal frequency of paradoxical sleep IAGP N RGD:5509061 20141003 MGI PMID:15581736 10802 Il6 interleukin 6 gene MP:0003278 esophageal inflammation IAGP N RGD:5509061 20141003 MGI PMID:22264787 10802 Il6 interleukin 6 gene MP:0003326 liver failure IAGP N RGD:5509061 20141003 MGI PMID:8910279 10802 Il6 interleukin 6 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24332041 10802 Il6 interleukin 6 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:24012418 10802 Il6 interleukin 6 gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:16843000 10802 Il6 interleukin 6 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:19436757 10802 Il6 interleukin 6 gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10712626 10802 Il6 interleukin 6 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:19234091 10802 Il6 interleukin 6 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17314284 10802 Il6 interleukin 6 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12957371 10802 Il6 interleukin 6 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:24012418 10802 Il6 interleukin 6 gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20141003 MGI PMID:8551238 10802 Il6 interleukin 6 gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20141003 MGI PMID:9688988 10802 Il6 interleukin 6 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19436757 10802 Il6 interleukin 6 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17615358 10802 Il6 interleukin 6 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:17581588 10802 Il6 interleukin 6 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15831701 10802 Il6 interleukin 6 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19436757 10802 Il6 interleukin 6 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:11006436 10802 Il6 interleukin 6 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:19918056 10802 Il6 interleukin 6 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:17581588 10802 Il6 interleukin 6 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8127368 10802 Il6 interleukin 6 gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:20483735 10802 Il6 interleukin 6 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9169772 10802 Il6 interleukin 6 gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:8127368 10802 Il6 interleukin 6 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19234091 10802 Il6 interleukin 6 gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9284817 10802 Il6 interleukin 6 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:10712626 10802 Il6 interleukin 6 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:11208530 10802 Il6 interleukin 6 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:18423196 10802 Il6 interleukin 6 gene MP:0005167 abnormal blood-brain barrier function IAGP N RGD:5509061 20141003 MGI PMID:10415153 10802 Il6 interleukin 6 gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:14988384 10802 Il6 interleukin 6 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18719127 10802 Il6 interleukin 6 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19234091 10802 Il6 interleukin 6 gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:8666893 10802 Il6 interleukin 6 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:12223557 10802 Il6 interleukin 6 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:9688988 10802 Il6 interleukin 6 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:8666893 10802 Il6 interleukin 6 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:8666893 10802 Il6 interleukin 6 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:8910279 10802 Il6 interleukin 6 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:15581736 10802 Il6 interleukin 6 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:18367337 10802 Il6 interleukin 6 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:14988384 10802 Il6 interleukin 6 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220714 MGI PMID:31664153 10802 Il6 interleukin 6 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:9875345 10802 Il6 interleukin 6 gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:12456808 10802 Il6 interleukin 6 gene MP:0008046 absent NK cells IAGP N RGD:5509061 20141003 MGI PMID:9169772 10802 Il6 interleukin 6 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17581588 10802 Il6 interleukin 6 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15831701 10802 Il6 interleukin 6 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:11018077 10802 Il6 interleukin 6 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:11018077 10802 Il6 interleukin 6 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:8666893 10802 Il6 interleukin 6 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:18378582 10802 Il6 interleukin 6 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:12219085 10802 Il6 interleukin 6 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17581589 10802 Il6 interleukin 6 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:8666893 10802 Il6 interleukin 6 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:17581588 10802 Il6 interleukin 6 gene MP:0008618 decreased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:8666893 10802 Il6 interleukin 6 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:17581588 10802 Il6 interleukin 6 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:20083667 10802 Il6 interleukin 6 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:17581589 10802 Il6 interleukin 6 gene MP:0008704 abnormal interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:16581004 10802 Il6 interleukin 6 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:11208530 10802 Il6 interleukin 6 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:21148800 10802 Il6 interleukin 6 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:9169772 10802 Il6 interleukin 6 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:10415153 10802 Il6 interleukin 6 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23085146 10802 Il6 interleukin 6 gene MP:0009410 abnormal skeletal muscle satellite cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18177723 10802 Il6 interleukin 6 gene MP:0009753 enhanced behavioral response to morphine IAGP N RGD:5509061 20141003 MGI PMID:10215902 10802 Il6 interleukin 6 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:8910279 10802 Il6 interleukin 6 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9688988 10802 Il6 interleukin 6 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18264109 10802 Il6 interleukin 6 gene MP:0009978 abnormal cerebellum white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:10415153 10802 Il6 interleukin 6 gene MP:0010042 abnormal oval cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11120777 10802 Il6 interleukin 6 gene MP:0010119 abnormal bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:11018077 10802 Il6 interleukin 6 gene MP:0010211 abnormal acute phase protein level IAGP N RGD:5509061 20141003 MGI PMID:8127368 10802 Il6 interleukin 6 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24332041 10802 Il6 interleukin 6 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23085146 10802 Il6 interleukin 6 gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:12358740 10802 Il6 interleukin 6 gene MP:0012563 increased tumor incidence following infection IAGP N RGD:5509061 20241114 MGI PMID:36103821 10802 Il6 interleukin 6 gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20141003 MGI PMID:12358740 10802 Il6 interleukin 6 gene MP:0014190 abnormal epididymis physiology IAGP N RGD:5509061 20220714 MGI PMID:31664153 10802 Il6 interleukin 6 gene MP:0014315 decreased heart left ventricle anterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:19234091 10802 Il6 interleukin 6 gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:19234091 10802 Il6 interleukin 6 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:19378383 10802 Il6 interleukin 6 gene MP:0020340 abnormal inhibitory learning IAGP N RGD:5509061 20160915 MGI PMID:19378383 10802 Il6 interleukin 6 gene MP:0020928 increased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:8127368 10802 Il6 interleukin 6 gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:19234091 10802 Il6 interleukin 6 gene MP:0030587 abnormal pancreatic alpha cell mass IAGP N RGD:5509061 20180614 MGI PMID:18719127 10802 Il6 interleukin 6 gene MP:0030945 abnormal myoblast migration IAGP N RGD:5509061 20190725 MGI PMID:18177723 10802 Il6 interleukin 6 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:12946594 10802 Il6 interleukin 6 gene MP:0031425 enhanced male fertility IAGP N RGD:5509061 20220714 MGI PMID:31664153 10802 Il6 interleukin 6 gene MP:0031426 increased sperm motility IAGP N RGD:5509061 20220714 MGI PMID:31664153 10802 Il6 interleukin 6 gene MP:0031427 increased sperm progressive motility IAGP N RGD:5509061 20220714 MGI PMID:31664153 10803 Il6ra interleukin 6 receptor, alpha gene MP:0000436 abnormal head movements IAGP N RGD:5509061 20141003 MGI PMID:23085146 10803 Il6ra interleukin 6 receptor, alpha gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23378927 10803 Il6ra interleukin 6 receptor, alpha gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23378927 10803 Il6ra interleukin 6 receptor, alpha gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:20483735 10803 Il6ra interleukin 6 receptor, alpha gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:23954788 10803 Il6ra interleukin 6 receptor, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20483735 10803 Il6ra interleukin 6 receptor, alpha gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:23085146 10803 Il6ra interleukin 6 receptor, alpha gene MP:0002714 increased glycogen catabolism rate IAGP N RGD:5509061 20141003 MGI PMID:20816090 10803 Il6ra interleukin 6 receptor, alpha gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20816090 10803 Il6ra interleukin 6 receptor, alpha gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20816090 10803 Il6ra interleukin 6 receptor, alpha gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23954788 10803 Il6ra interleukin 6 receptor, alpha gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23954788 10803 Il6ra interleukin 6 receptor, alpha gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23954788 10803 Il6ra interleukin 6 receptor, alpha gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23954788 10803 Il6ra interleukin 6 receptor, alpha gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23378927 10803 Il6ra interleukin 6 receptor, alpha gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:20483735 10803 Il6ra interleukin 6 receptor, alpha gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:22467660 10803 Il6ra interleukin 6 receptor, alpha gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:20483735 10803 Il6ra interleukin 6 receptor, alpha gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20816090 10803 Il6ra interleukin 6 receptor, alpha gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:20816090 10803 Il6ra interleukin 6 receptor, alpha gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23954788 10803 Il6ra interleukin 6 receptor, alpha gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20816090 10803 Il6ra interleukin 6 receptor, alpha gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20083667 10803 Il6ra interleukin 6 receptor, alpha gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:23378927 10803 Il6ra interleukin 6 receptor, alpha gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:23378927 10803 Il6ra interleukin 6 receptor, alpha gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:20816090 10803 Il6ra interleukin 6 receptor, alpha gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22467660 10803 Il6ra interleukin 6 receptor, alpha gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20816090 10803 Il6ra interleukin 6 receptor, alpha gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:22467660 10803 Il6ra interleukin 6 receptor, alpha gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 10803 Il6ra interleukin 6 receptor, alpha gene MP:0010214 abnormal circulating serum amyloid protein level IAGP N RGD:5509061 20141003 MGI PMID:23378927 10803 Il6ra interleukin 6 receptor, alpha gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:20816090 10803 Il6ra interleukin 6 receptor, alpha gene MP:0010751 decreased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22467660 10803 Il6ra interleukin 6 receptor, alpha gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23085146 10803 Il6ra interleukin 6 receptor, alpha gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:20816090 10804 Kpnb1 karyopherin subunit beta 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16414015 10804 Kpnb1 karyopherin subunit beta 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20151112 MGI PMID:22841314 10804 Kpnb1 karyopherin subunit beta 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16414015 10806 Ina internexin neuronal intermediate filament protein, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10350642 10806 Ina internexin neuronal intermediate filament protein, alpha gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:17005864 10808 Inha inhibin alpha gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:8090730 10808 Inha inhibin alpha gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:8090730 10808 Inha inhibin alpha gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0001123 dilated uterus IAGP N RGD:5509061 20141003 MGI PMID:8895659 10808 Inha inhibin alpha gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20230629 MGI PMID:35255139 10808 Inha inhibin alpha gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:17652186 10808 Inha inhibin alpha gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:1448148 10808 Inha inhibin alpha gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:1448148 10808 Inha inhibin alpha gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:1448148 10808 Inha inhibin alpha gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8090730 10808 Inha inhibin alpha gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8090730 10808 Inha inhibin alpha gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:1448148 10808 Inha inhibin alpha gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20230629 MGI PMID:35255139 10808 Inha inhibin alpha gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:1448148 10808 Inha inhibin alpha gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:1448148 10808 Inha inhibin alpha gene MP:0001934 increased litter size IAGP N RGD:5509061 20230629 MGI PMID:35255139 10808 Inha inhibin alpha gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:8895659 10808 Inha inhibin alpha gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8895659 10808 Inha inhibin alpha gene MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17652186 10808 Inha inhibin alpha gene MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8090730 10808 Inha inhibin alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8828479 10808 Inha inhibin alpha gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0002776 increased Sertoli cell number IAGP N RGD:5509061 20220630 MGI PMID:17652186 10808 Inha inhibin alpha gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:8895659 10808 Inha inhibin alpha gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0003718 maternal effect IAGP N RGD:5509061 20230629 MGI PMID:35255139 10808 Inha inhibin alpha gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:1448148 10808 Inha inhibin alpha gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17652186 10808 Inha inhibin alpha gene MP:0004855 increased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:17652186 10808 Inha inhibin alpha gene MP:0004855 increased ovary weight IAGP N RGD:5509061 20230629 MGI PMID:35255139 10808 Inha inhibin alpha gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20230629 MGI PMID:35255139 10808 Inha inhibin alpha gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:8090730 10808 Inha inhibin alpha gene MP:0005151 diffuse hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:8090730 10808 Inha inhibin alpha gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:8090730 10808 Inha inhibin alpha gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17652186 10808 Inha inhibin alpha gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8895659 10808 Inha inhibin alpha gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:1448148 10808 Inha inhibin alpha gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17652186 10808 Inha inhibin alpha gene MP:0009257 dilated seminiferous tubule IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0009590 increased gonad tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:1448148 10808 Inha inhibin alpha gene MP:0009592 increased Leydig cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8895659 10808 Inha inhibin alpha gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:12855748 10808 Inha inhibin alpha gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:8090730 10808 Inha inhibin alpha gene MP:0011124 increased primary ovarian follicle number IAGP N RGD:5509061 20230629 MGI PMID:35255139 10808 Inha inhibin alpha gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8895659 10808 Inha inhibin alpha gene MP:0031301 chronic liver inflammation IAGP N RGD:5509061 20211028 MGI PMID:8090730 10808 Inha inhibin alpha gene MP:0031407 increased Sertoli cell proliferation IAGP N RGD:5509061 20220630 MGI PMID:17652186 10808 Inha inhibin alpha gene MP:0031411 increased ovulation rate IAGP N RGD:5509061 20230629 MGI PMID:35255139 10808 Inha inhibin alpha gene MP:0031421 increased superovulation rate IAGP N RGD:5509061 20230629 MGI PMID:35255139 10808 Inha inhibin alpha gene MP:0031424 enhanced female fertility IAGP N RGD:5509061 20230629 MGI PMID:35255139 10810 Inhbb inhibin beta-B gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:7885473 10810 Inhbb inhibin beta-B gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8125256 10810 Inhbb inhibin beta-B gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17609433 10810 Inhbb inhibin beta-B gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:7885473 10810 Inhbb inhibin beta-B gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:8125256 10810 Inhbb inhibin beta-B gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:7885473 10810 Inhbb inhibin beta-B gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:8125256 10810 Inhbb inhibin beta-B gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:8125256 10810 Inhbb inhibin beta-B gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:7947320 10810 Inhbb inhibin beta-B gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:8125256 10810 Inhbb inhibin beta-B gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:7947320 10810 Inhbb inhibin beta-B gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:7947320 10810 Inhbb inhibin beta-B gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210128 MGI 10810 Inhbb inhibin beta-B gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 10810 Inhbb inhibin beta-B gene MP:0001406 abnormal gait IEA N RGD:5509061 20210128 MGI 10810 Inhbb inhibin beta-B gene MP:0001523 impaired righting response IEA N RGD:5509061 20210128 MGI 10810 Inhbb inhibin beta-B gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20210128 MGI 10810 Inhbb inhibin beta-B gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:8125256 10810 Inhbb inhibin beta-B gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17609433 10810 Inhbb inhibin beta-B gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:8125256 10810 Inhbb inhibin beta-B gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17609433 10810 Inhbb inhibin beta-B gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17609433 10810 Inhbb inhibin beta-B gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:8125256 10810 Inhbb inhibin beta-B gene MP:0002293 long gestation period IAGP N RGD:5509061 20141003 MGI PMID:8125256 10810 Inhbb inhibin beta-B gene MP:0002681 increased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:17609433 10810 Inhbb inhibin beta-B gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 10810 Inhbb inhibin beta-B gene MP:0003153 early eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:7947320 10810 Inhbb inhibin beta-B gene MP:0003346 abnormal pectoral muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:20810712 10810 Inhbb inhibin beta-B gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:17609433 10810 Inhbb inhibin beta-B gene MP:0004855 increased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:17609433 10810 Inhbb inhibin beta-B gene MP:0005131 increased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17609433 10810 Inhbb inhibin beta-B gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:7947320 10810 Inhbb inhibin beta-B gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8125256 10810 Inhbb inhibin beta-B gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:8125256 10810 Inhbb inhibin beta-B gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17609433 10810 Inhbb inhibin beta-B gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20220407 MGI PMID:17609433 10810 Inhbb inhibin beta-B gene MP:0009505 abnormal mammary gland lobule morphology IAGP N RGD:5509061 20150402 MGI PMID:8125256 10810 Inhbb inhibin beta-B gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:7885473 10810 Inhbb inhibin beta-B gene MP:0010238 increased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:20810712 10810 Inhbb inhibin beta-B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8125256 10810 Inhbb inhibin beta-B gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7885473 10810 Inhbb inhibin beta-B gene MP:0013718 galactostasis IAGP N RGD:5509061 20150402 MGI PMID:8125256 10811 Ins1 insulin I gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180719 MGI PMID:9144203 10811 Ins1 insulin I gene MP:0001265 decreased body size IAGP N RGD:5509061 20180719 MGI PMID:9144203 10811 Ins1 insulin I gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20180719 MGI PMID:9144203 10811 Ins1 insulin I gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20180719 MGI PMID:19680229 10811 Ins1 insulin I gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20180719 MGI PMID:19680229 10811 Ins1 insulin I gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20180719 MGI PMID:9144203 10811 Ins1 insulin I gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20180719 MGI PMID:19680229 10811 Ins1 insulin I gene MP:0001844 autoimmune response IAGP N RGD:5509061 20180719 MGI PMID:15889095 10811 Ins1 insulin I gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20180719 MGI PMID:19680229 10811 Ins1 insulin I gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20180719 MGI PMID:15889095 10811 Ins1 insulin I gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180719 MGI PMID:11272179 10811 Ins1 insulin I gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180719 MGI PMID:9144203 10811 Ins1 insulin I gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26769314 10811 Ins1 insulin I gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20180719 MGI PMID:19680229 10811 Ins1 insulin I gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180719 MGI PMID:9144203 10811 Ins1 insulin I gene MP:0002869 increased anti-insulin autoantibody level IAGP N RGD:5509061 20180719 MGI PMID:19680229 10811 Ins1 insulin I gene MP:0002870 decreased anti-insulin autoantibody level IAGP N RGD:5509061 20180719 MGI PMID:15889095 10811 Ins1 insulin I gene MP:0003031 acidosis IAGP N RGD:5509061 20180719 MGI PMID:9144203 10811 Ins1 insulin I gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20210617 MGI PMID:29864031 10811 Ins1 insulin I gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20210617 MGI PMID:29864031 10811 Ins1 insulin I gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20180719 MGI PMID:19680229 10811 Ins1 insulin I gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20180719 MGI PMID:19680229 10811 Ins1 insulin I gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20180719 MGI PMID:11272179 10811 Ins1 insulin I gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180719 MGI PMID:9144203 10811 Ins1 insulin I gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20180719 MGI PMID:15889095 10811 Ins1 insulin I gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20180719 MGI PMID:12925730 10811 Ins1 insulin I gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20180719 MGI PMID:15889095 10811 Ins1 insulin I gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210617 MGI PMID:29864031 10811 Ins1 insulin I gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20180719 MGI PMID:15889095 10811 Ins1 insulin I gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20180719 MGI PMID:19680229 10811 Ins1 insulin I gene MP:0008559 abnormal interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:19680229 10811 Ins1 insulin I gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20180719 MGI PMID:11272179 10811 Ins1 insulin I gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20180719 MGI PMID:11897712 10811 Ins1 insulin I gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20180719 MGI PMID:11897712 10811 Ins1 insulin I gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20180719 MGI PMID:9144203 10811 Ins1 insulin I gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20180719 MGI PMID:11897712 10811 Ins1 insulin I gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20180719 MGI PMID:11897712 10811 Ins1 insulin I gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:19680229 10811 Ins1 insulin I gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:9144203 10811 Ins1 insulin I gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:11897712 10811 Ins1 insulin I gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20210617 MGI PMID:29864031 10811 Ins1 insulin I gene MP:0014109 increased pancreatic alpha cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:11897712 10811 Ins1 insulin I gene MP:0014122 decreased pancreatic islet cell apoptosis IAGP N RGD:5509061 20180719 MGI PMID:11897712 10811 Ins1 insulin I gene MP:0014122 decreased pancreatic islet cell apoptosis IAGP N RGD:5509061 20180719 MGI PMID:25830089 10811 Ins1 insulin I gene MP:0030589 increased pancreatic alpha cell mass IAGP N RGD:5509061 20180719 MGI PMID:11897712 10812 Ins2 insulin II gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16604193 10812 Ins2 insulin II gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15914643 10812 Ins2 insulin II gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16604193 10812 Ins2 insulin II gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21606463 10812 Ins2 insulin II gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15731364 10812 Ins2 insulin II gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16964447 10812 Ins2 insulin II gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20170413 MGI PMID:27820699 10812 Ins2 insulin II gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15914643 10812 Ins2 insulin II gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18563383 10812 Ins2 insulin II gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18563383 10812 Ins2 insulin II gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16604193 10812 Ins2 insulin II gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16604193 10812 Ins2 insulin II gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:9133560 10812 Ins2 insulin II gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:9144203 10812 Ins2 insulin II gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16964447 10812 Ins2 insulin II gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15914643 10812 Ins2 insulin II gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17303807 10812 Ins2 insulin II gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17334640 10812 Ins2 insulin II gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21606463 10812 Ins2 insulin II gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22297672 10812 Ins2 insulin II gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23410753 10812 Ins2 insulin II gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240801 MGI PMID:35108512 10812 Ins2 insulin II gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9144203 10812 Ins2 insulin II gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17334640 10812 Ins2 insulin II gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17334640 10812 Ins2 insulin II gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:9133560 10812 Ins2 insulin II gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:15587270 10812 Ins2 insulin II gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:17334640 10812 Ins2 insulin II gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21606463 10812 Ins2 insulin II gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9144203 10812 Ins2 insulin II gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21606463 10812 Ins2 insulin II gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:11981430 10812 Ins2 insulin II gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15914643 10812 Ins2 insulin II gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17303807 10812 Ins2 insulin II gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17334640 10812 Ins2 insulin II gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:18056790 10812 Ins2 insulin II gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:18563383 10812 Ins2 insulin II gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19680229 10812 Ins2 insulin II gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19955657 10812 Ins2 insulin II gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21606463 10812 Ins2 insulin II gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:22297672 10812 Ins2 insulin II gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:9133560 10812 Ins2 insulin II gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:9593767 10812 Ins2 insulin II gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20201224 MGI PMID:32699230 10812 Ins2 insulin II gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19680229 10812 Ins2 insulin II gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15587270 10812 Ins2 insulin II gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9133560 10812 Ins2 insulin II gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:15587270 10812 Ins2 insulin II gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:17303807 10812 Ins2 insulin II gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:9144203 10812 Ins2 insulin II gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:9133560 10812 Ins2 insulin II gene MP:0001762 polyuria IAGP N RGD:5509061 20201224 MGI PMID:32699230 10812 Ins2 insulin II gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20201224 MGI PMID:32699230 10812 Ins2 insulin II gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:19680229 10812 Ins2 insulin II gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:15889095 10812 Ins2 insulin II gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:19680229 10812 Ins2 insulin II gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:15889095 10812 Ins2 insulin II gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11272179 10812 Ins2 insulin II gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12925730 10812 Ins2 insulin II gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18563383 10812 Ins2 insulin II gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9144203 10812 Ins2 insulin II gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20210422 MGI PMID:32640216 10812 Ins2 insulin II gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16964447 10812 Ins2 insulin II gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9593767 10812 Ins2 insulin II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11981430 10812 Ins2 insulin II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16604193 10812 Ins2 insulin II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17303807 10812 Ins2 insulin II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21606463 10812 Ins2 insulin II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22297672 10812 Ins2 insulin II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9133560 10812 Ins2 insulin II gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19684026 10812 Ins2 insulin II gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15914643 10812 Ins2 insulin II gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16604193 10812 Ins2 insulin II gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19680229 10812 Ins2 insulin II gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:15587270 10812 Ins2 insulin II gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15587270 10812 Ins2 insulin II gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:9144203 10812 Ins2 insulin II gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:17334640 10812 Ins2 insulin II gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:19955657 10812 Ins2 insulin II gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17303807 10812 Ins2 insulin II gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19955657 10812 Ins2 insulin II gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21606463 10812 Ins2 insulin II gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9133560 10812 Ins2 insulin II gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20240801 MGI PMID:35108512 10812 Ins2 insulin II gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16604193 10812 Ins2 insulin II gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15914643 10812 Ins2 insulin II gene MP:0002869 increased anti-insulin autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:12925730 10812 Ins2 insulin II gene MP:0002869 increased anti-insulin autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:15889095 10812 Ins2 insulin II gene MP:0002869 increased anti-insulin autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:19680229 10812 Ins2 insulin II gene MP:0002870 decreased anti-insulin autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:15889095 10812 Ins2 insulin II gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:22297672 10812 Ins2 insulin II gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11981430 10812 Ins2 insulin II gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0003031 acidosis IAGP N RGD:5509061 20141003 MGI PMID:9144203 10812 Ins2 insulin II gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20150611 MGI PMID:11272179 10812 Ins2 insulin II gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19955657 10812 Ins2 insulin II gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20308425 10812 Ins2 insulin II gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:23410753 10812 Ins2 insulin II gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:9133560 10812 Ins2 insulin II gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:9593767 10812 Ins2 insulin II gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20150611 MGI PMID:17303807 10812 Ins2 insulin II gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:15914643 10812 Ins2 insulin II gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18563383 10812 Ins2 insulin II gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:15587270 10812 Ins2 insulin II gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:17303807 10812 Ins2 insulin II gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:19680229 10812 Ins2 insulin II gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:23410753 10812 Ins2 insulin II gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20240801 MGI PMID:35108512 10812 Ins2 insulin II gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17303807 10812 Ins2 insulin II gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19680229 10812 Ins2 insulin II gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:11272179 10812 Ins2 insulin II gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9144203 10812 Ins2 insulin II gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:12925730 10812 Ins2 insulin II gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:16804066 10812 Ins2 insulin II gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:17303807 10812 Ins2 insulin II gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:15889095 10812 Ins2 insulin II gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20240801 MGI PMID:35108512 10812 Ins2 insulin II gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21606463 10812 Ins2 insulin II gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21606463 10812 Ins2 insulin II gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:17303807 10812 Ins2 insulin II gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:18563383 10812 Ins2 insulin II gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:23410753 10812 Ins2 insulin II gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20201224 MGI PMID:32699230 10812 Ins2 insulin II gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20240801 MGI PMID:35108512 10812 Ins2 insulin II gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9593767 10812 Ins2 insulin II gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17303807 10812 Ins2 insulin II gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9593767 10812 Ins2 insulin II gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20201224 MGI PMID:32699230 10812 Ins2 insulin II gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15914643 10812 Ins2 insulin II gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:22297672 10812 Ins2 insulin II gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20308425 10812 Ins2 insulin II gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21606463 10812 Ins2 insulin II gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23410753 10812 Ins2 insulin II gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:9133560 10812 Ins2 insulin II gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20201224 MGI PMID:32699230 10812 Ins2 insulin II gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20240801 MGI PMID:35108512 10812 Ins2 insulin II gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17303807 10812 Ins2 insulin II gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:21606463 10812 Ins2 insulin II gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18563383 10812 Ins2 insulin II gene MP:0005527 increased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:22297672 10812 Ins2 insulin II gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15889095 10812 Ins2 insulin II gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16804066 10812 Ins2 insulin II gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16964447 10812 Ins2 insulin II gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17303807 10812 Ins2 insulin II gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19680229 10812 Ins2 insulin II gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19955657 10812 Ins2 insulin II gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20308425 10812 Ins2 insulin II gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23410753 10812 Ins2 insulin II gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20210422 MGI PMID:32640216 10812 Ins2 insulin II gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23410753 10812 Ins2 insulin II gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:11981430 10812 Ins2 insulin II gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:16604193 10812 Ins2 insulin II gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15914643 10812 Ins2 insulin II gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:16604193 10812 Ins2 insulin II gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:18563383 10812 Ins2 insulin II gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:18563383 10812 Ins2 insulin II gene MP:0008559 abnormal interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19680229 10812 Ins2 insulin II gene MP:0008817 hematoma IAGP N RGD:5509061 20141003 MGI PMID:21258336 10812 Ins2 insulin II gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16604193 10812 Ins2 insulin II gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0009112 abnormal pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:19955657 10812 Ins2 insulin II gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:11272179 10812 Ins2 insulin II gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:11897712 10812 Ins2 insulin II gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:19955657 10812 Ins2 insulin II gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20210422 MGI PMID:32640216 10812 Ins2 insulin II gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:11897712 10812 Ins2 insulin II gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:9144203 10812 Ins2 insulin II gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:15587270 10812 Ins2 insulin II gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:20308425 10812 Ins2 insulin II gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:9593767 10812 Ins2 insulin II gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20201224 MGI PMID:32699230 10812 Ins2 insulin II gene MP:0009174 absent pancreatic beta cells IAGP N RGD:5509061 20141003 MGI PMID:15587270 10812 Ins2 insulin II gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:17303807 10812 Ins2 insulin II gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:15587270 10812 Ins2 insulin II gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:17303807 10812 Ins2 insulin II gene MP:0009255 degranulated pancreatic beta cells IAGP N RGD:5509061 20141003 MGI PMID:9593767 10812 Ins2 insulin II gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:11897712 10812 Ins2 insulin II gene MP:0009488 abnormal pancreatic islet cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19955657 10812 Ins2 insulin II gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:11897712 10812 Ins2 insulin II gene MP:0010145 abnormal spermatic cord morphology IAGP N RGD:5509061 20220324 MGI PMID:16604193 10812 Ins2 insulin II gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20240801 MGI PMID:35108512 10812 Ins2 insulin II gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15587270 10812 Ins2 insulin II gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18563383 10812 Ins2 insulin II gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19680229 10812 Ins2 insulin II gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9144203 10812 Ins2 insulin II gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:22297672 10812 Ins2 insulin II gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:22297672 10812 Ins2 insulin II gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:22297672 10812 Ins2 insulin II gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:22297672 10812 Ins2 insulin II gene MP:0011425 abnormal kidney interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:22297672 10812 Ins2 insulin II gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:22297672 10812 Ins2 insulin II gene MP:0011638 abnormal mitochondrial chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:16604193 10812 Ins2 insulin II gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20180614 MGI PMID:11897712 10812 Ins2 insulin II gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20210422 MGI PMID:32640216 10812 Ins2 insulin II gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:23410753 10812 Ins2 insulin II gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:17334640 10812 Ins2 insulin II gene MP:0014109 increased pancreatic alpha cell proliferation IAGP N RGD:5509061 20180614 MGI PMID:11897712 10812 Ins2 insulin II gene MP:0014117 increased pancreatic beta cell apoptosis IAGP N RGD:5509061 20210422 MGI PMID:32640216 10812 Ins2 insulin II gene MP:0014121 increased pancreatic islet cell apoptosis IAGP N RGD:5509061 20160324 MGI PMID:19955657 10812 Ins2 insulin II gene MP:0014122 decreased pancreatic islet cell apoptosis IAGP N RGD:5509061 20180614 MGI PMID:11897712 10812 Ins2 insulin II gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20170803 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:22297672 10812 Ins2 insulin II gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:15914643 10812 Ins2 insulin II gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0030589 increased pancreatic alpha cell mass IAGP N RGD:5509061 20180614 MGI PMID:11897712 10812 Ins2 insulin II gene MP:0031414 decreased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:17911348 10812 Ins2 insulin II gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:17911348 10813 Insr insulin receptor gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11000114 10813 Insr insulin receptor gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18288891 10813 Insr insulin receptor gene MP:0000199 abnormal circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20200402 MGI PMID:11877471 10813 Insr insulin receptor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20211118 MGI PMID:27374329 10813 Insr insulin receptor gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:8612577 10813 Insr insulin receptor gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:15713666 10813 Insr insulin receptor gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20211118 MGI PMID:27374329 10813 Insr insulin receptor gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:23119079 10813 Insr insulin receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:23119079 10813 Insr insulin receptor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11000114 10813 Insr insulin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11000114 10813 Insr insulin receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12459269 10813 Insr insulin receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17416680 10813 Insr insulin receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8612577 10813 Insr insulin receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12459269 10813 Insr insulin receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:17416680 10813 Insr insulin receptor gene MP:0001426 polydipsia IAGP N RGD:5509061 20180628 MGI PMID:26868295 10813 Insr insulin receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:11000114 10813 Insr insulin receptor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20200402 MGI PMID:11877471 10813 Insr insulin receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11000114 10813 Insr insulin receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:8612577 10813 Insr insulin receptor gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20191226 MGI PMID:8612577 10813 Insr insulin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:11463843 10813 Insr insulin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15713666 10813 Insr insulin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17416680 10813 Insr insulin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:23119079 10813 Insr insulin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:8528241 10813 Insr insulin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:8612577 10813 Insr insulin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:9844629 10813 Insr insulin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20180628 MGI PMID:26868295 10813 Insr insulin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20211118 MGI PMID:27374329 10813 Insr insulin receptor gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18288891 10813 Insr insulin receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15713666 10813 Insr insulin receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:12459269 10813 Insr insulin receptor gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20180628 MGI PMID:26868295 10813 Insr insulin receptor gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20191226 MGI PMID:8612577 10813 Insr insulin receptor gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:17416680 10813 Insr insulin receptor gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:23119079 10813 Insr insulin receptor gene MP:0001868 ovary inflammation IAGP N RGD:5509061 20141003 MGI PMID:23119079 10813 Insr insulin receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11000114 10813 Insr insulin receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12219087 10813 Insr insulin receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12488434 10813 Insr insulin receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16581004 10813 Insr insulin receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200402 MGI PMID:11877471 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11000114 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11463843 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15713666 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17416680 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18288891 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18477811 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22055502 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:8528241 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:8612577 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9844629 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180628 MGI PMID:26868295 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20211118 MGI PMID:27374329 10813 Insr insulin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20220811 MGI PMID:34460911 10813 Insr insulin receptor gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12219087 10813 Insr insulin receptor gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12459269 10813 Insr insulin receptor gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12488434 10813 Insr insulin receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17416680 10813 Insr insulin receptor gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200402 MGI PMID:11877471 10813 Insr insulin receptor gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0002188 small heart IAGP N RGD:5509061 20200402 MGI PMID:11877471 10813 Insr insulin receptor gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:14628051 10813 Insr insulin receptor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11000114 10813 Insr insulin receptor gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12459269 10813 Insr insulin receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:8528241 10813 Insr insulin receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:8612577 10813 Insr insulin receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:11000114 10813 Insr insulin receptor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11000114 10813 Insr insulin receptor gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:11000114 10813 Insr insulin receptor gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20220811 MGI PMID:34460911 10813 Insr insulin receptor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0002865 increased growth rate IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15713666 10813 Insr insulin receptor gene MP:0002893 ketoaciduria IAGP N RGD:5509061 20141003 MGI PMID:11463843 10813 Insr insulin receptor gene MP:0002893 ketoaciduria IAGP N RGD:5509061 20141003 MGI PMID:12459269 10813 Insr insulin receptor gene MP:0002893 ketoaciduria IAGP N RGD:5509061 20141003 MGI PMID:8528241 10813 Insr insulin receptor gene MP:0002893 ketoaciduria IAGP N RGD:5509061 20141003 MGI PMID:8612577 10813 Insr insulin receptor gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:14628051 10813 Insr insulin receptor gene MP:0002996 ovotestis IAGP N RGD:5509061 20141003 MGI PMID:14628051 10813 Insr insulin receptor gene MP:0003023 decreased coronary flow rate IAGP N RGD:5509061 20200402 MGI PMID:11877471 10813 Insr insulin receptor gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:18477811 10813 Insr insulin receptor gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17416680 10813 Insr insulin receptor gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:23119079 10813 Insr insulin receptor gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20200402 MGI PMID:11877471 10813 Insr insulin receptor gene MP:0003839 abnormal insulin clearance IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0003916 decreased heart left ventricle weight IAGP N RGD:5509061 20231109 MGI PMID:11877471 10813 Insr insulin receptor gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0003959 abnormal lean body mass IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23119079 10813 Insr insulin receptor gene MP:0004039 abnormal cardiac muscle cell glucose uptake IAGP N RGD:5509061 20200402 MGI PMID:11877471 10813 Insr insulin receptor gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20200402 MGI PMID:11877471 10813 Insr insulin receptor gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:15372107 10813 Insr insulin receptor gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:9844629 10813 Insr insulin receptor gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18288891 10813 Insr insulin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11463843 10813 Insr insulin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15713666 10813 Insr insulin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17416680 10813 Insr insulin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18477811 10813 Insr insulin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180628 MGI PMID:26868295 10813 Insr insulin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20211118 MGI PMID:27374329 10813 Insr insulin receptor gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12459269 10813 Insr insulin receptor gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9844629 10813 Insr insulin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11000114 10813 Insr insulin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15713666 10813 Insr insulin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17416680 10813 Insr insulin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:18288891 10813 Insr insulin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22055502 10813 Insr insulin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180628 MGI PMID:26868295 10813 Insr insulin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20211118 MGI PMID:27374329 10813 Insr insulin receptor gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:9844629 10813 Insr insulin receptor gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:23119079 10813 Insr insulin receptor gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:12459269 10813 Insr insulin receptor gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:23119079 10813 Insr insulin receptor gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15372107 10813 Insr insulin receptor gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:11000114 10813 Insr insulin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12459269 10813 Insr insulin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12219087 10813 Insr insulin receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17416680 10813 Insr insulin receptor gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20211118 MGI PMID:27374329 10813 Insr insulin receptor gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11000114 10813 Insr insulin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23119079 10813 Insr insulin receptor gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23119079 10813 Insr insulin receptor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0006353 increased glycosylated hemoglobin level IEA N RGD:5509061 20111116 MGI 10813 Insr insulin receptor gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20190103 MGI 10813 Insr insulin receptor gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:15372107 10813 Insr insulin receptor gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:17416680 10813 Insr insulin receptor gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:18288891 10813 Insr insulin receptor gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20180628 MGI PMID:26868295 10813 Insr insulin receptor gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:17416680 10813 Insr insulin receptor gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:18288891 10813 Insr insulin receptor gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20180614 MGI PMID:15372107 10813 Insr insulin receptor gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0009174 absent pancreatic beta cells IAGP N RGD:5509061 20180614 MGI PMID:12488434 10813 Insr insulin receptor gene MP:0009342 enlarged gallbladder IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0009462 skeletal muscle hypotrophy IAGP N RGD:5509061 20141003 MGI PMID:8612577 10813 Insr insulin receptor gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17416680 10813 Insr insulin receptor gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15713666 10813 Insr insulin receptor gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15713666 10813 Insr insulin receptor gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12459269 10813 Insr insulin receptor gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15713666 10813 Insr insulin receptor gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20211118 MGI PMID:27374329 10813 Insr insulin receptor gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20220811 MGI PMID:34460911 10813 Insr insulin receptor gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20220811 MGI PMID:34460911 10813 Insr insulin receptor gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:12459269 10813 Insr insulin receptor gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:8612577 10813 Insr insulin receptor gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20211118 MGI PMID:27374329 10813 Insr insulin receptor gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11463843 10813 Insr insulin receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12459269 10813 Insr insulin receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15254588 10813 Insr insulin receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15713666 10813 Insr insulin receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17189427 10813 Insr insulin receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8528241 10813 Insr insulin receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8612577 10813 Insr insulin receptor gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:11000114 10813 Insr insulin receptor gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:10949030 10813 Insr insulin receptor gene MP:0011943 abnormal circadian feeding behavior IAGP N RGD:5509061 20141003 MGI PMID:21266328 10813 Insr insulin receptor gene MP:0013925 abnormal vascular plexus formation IAGP N RGD:5509061 20220811 MGI PMID:34460911 10813 Insr insulin receptor gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20200402 MGI PMID:11877471 10813 Insr insulin receptor gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:11877471 10813 Insr insulin receptor gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20170202 MGI PMID:23119079 10813 Insr insulin receptor gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20200402 MGI PMID:11877471 10813 Insr insulin receptor gene MP:0030020 decreased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20200402 MGI PMID:11877471 10813 Insr insulin receptor gene MP:0030971 ketoacidosis IAGP N RGD:5509061 20190815 MGI PMID:15713666 10813 Insr insulin receptor gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240321 MGI PMID:23119079 10813 Insr insulin receptor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:11877471 10813 Insr insulin receptor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:17189427 10815 Irf1 interferon regulatory factor 1 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:7957048 10815 Irf1 interferon regulatory factor 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:16541466 10815 Irf1 interferon regulatory factor 1 gene MP:0001573 abnormal circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:16410367 10815 Irf1 interferon regulatory factor 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:9317154 10815 Irf1 interferon regulatory factor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10346812 10815 Irf1 interferon regulatory factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16541466 10815 Irf1 interferon regulatory factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8402903 10815 Irf1 interferon regulatory factor 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:9317154 10815 Irf1 interferon regulatory factor 1 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16123129 10815 Irf1 interferon regulatory factor 1 gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10346812 10815 Irf1 interferon regulatory factor 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16541466 10815 Irf1 interferon regulatory factor 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:16541466 10815 Irf1 interferon regulatory factor 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16541466 10815 Irf1 interferon regulatory factor 1 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:9317154 10815 Irf1 interferon regulatory factor 1 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10346812 10815 Irf1 interferon regulatory factor 1 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15240709 10815 Irf1 interferon regulatory factor 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15240709 10815 Irf1 interferon regulatory factor 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:16541466 10815 Irf1 interferon regulatory factor 1 gene MP:0004798 decreased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:16541466 10815 Irf1 interferon regulatory factor 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12807824 10815 Irf1 interferon regulatory factor 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:12499398 10815 Irf1 interferon regulatory factor 1 gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20190110 MGI 10815 Irf1 interferon regulatory factor 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:8402903 10815 Irf1 interferon regulatory factor 1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IEA N RGD:5509061 20111116 MGI 10815 Irf1 interferon regulatory factor 1 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8402903 10815 Irf1 interferon regulatory factor 1 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12807824 10815 Irf1 interferon regulatory factor 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16541466 10815 Irf1 interferon regulatory factor 1 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:8402903 10815 Irf1 interferon regulatory factor 1 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7957048 10815 Irf1 interferon regulatory factor 1 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8885869 10815 Irf1 interferon regulatory factor 1 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20111116 MGI 10815 Irf1 interferon regulatory factor 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:9472983 10815 Irf1 interferon regulatory factor 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16541466 10815 Irf1 interferon regulatory factor 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8402903 10815 Irf1 interferon regulatory factor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:7957048 10815 Irf1 interferon regulatory factor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8402903 10815 Irf1 interferon regulatory factor 1 gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:9379011 10815 Irf1 interferon regulatory factor 1 gene MP:0008563 decreased interferon-alpha secretion IEA N RGD:5509061 20111116 MGI 10815 Irf1 interferon regulatory factor 1 gene MP:0008565 decreased interferon-beta secretion IEA N RGD:5509061 20111116 MGI 10815 Irf1 interferon regulatory factor 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15240709 10815 Irf1 interferon regulatory factor 1 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:9379011 10815 Irf1 interferon regulatory factor 1 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:12807824 10815 Irf1 interferon regulatory factor 1 gene MP:0008590 abnormal circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:12807824 10815 Irf1 interferon regulatory factor 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:12807824 10815 Irf1 interferon regulatory factor 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:9379011 10815 Irf1 interferon regulatory factor 1 gene MP:0008600 decreased circulating interleukin-2 level IAGP N RGD:5509061 20141003 MGI PMID:9379011 10815 Irf1 interferon regulatory factor 1 gene MP:0008601 abnormal circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:12807824 10815 Irf1 interferon regulatory factor 1 gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:9379011 10815 Irf1 interferon regulatory factor 1 gene MP:0008608 increased circulating interleukin-13 level IAGP N RGD:5509061 20141003 MGI PMID:12807824 10815 Irf1 interferon regulatory factor 1 gene MP:0008623 increased circulating interleukin-3 level IAGP N RGD:5509061 20141003 MGI PMID:9379011 10815 Irf1 interferon regulatory factor 1 gene MP:0008626 increased circulating interleukin-5 level IAGP N RGD:5509061 20141003 MGI PMID:12807824 10815 Irf1 interferon regulatory factor 1 gene MP:0008626 increased circulating interleukin-5 level IAGP N RGD:5509061 20141003 MGI PMID:9379011 10815 Irf1 interferon regulatory factor 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:12807824 10815 Irf1 interferon regulatory factor 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:9379011 10815 Irf1 interferon regulatory factor 1 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:8885869 10815 Irf1 interferon regulatory factor 1 gene MP:0009332 abnormal splenocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7957048 10815 Irf1 interferon regulatory factor 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15240709 10815 Irf1 interferon regulatory factor 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10346812 10815 Irf1 interferon regulatory factor 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15240709 10815 Irf1 interferon regulatory factor 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:10346812 10815 Irf1 interferon regulatory factor 1 gene MP:0020916 increased susceptibility to Herpesvirales infection IEA N RGD:5509061 20200430 MGI 10815 Irf1 interferon regulatory factor 1 gene MP:0020928 increased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16123129 10816 Irs1 insulin receptor substrate 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:10749573 10816 Irs1 insulin receptor substrate 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20074531 10816 Irs1 insulin receptor substrate 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20160929 MGI PMID:27534441 10816 Irs1 insulin receptor substrate 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10749573 10816 Irs1 insulin receptor substrate 1 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:10749573 10816 Irs1 insulin receptor substrate 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:14736890 10816 Irs1 insulin receptor substrate 1 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:10749573 10816 Irs1 insulin receptor substrate 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18590693 10816 Irs1 insulin receptor substrate 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9541510 10816 Irs1 insulin receptor substrate 1 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18590693 10816 Irs1 insulin receptor substrate 1 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:9541510 10816 Irs1 insulin receptor substrate 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14736890 10816 Irs1 insulin receptor substrate 1 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0000589 thin tail IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:20837540 10816 Irs1 insulin receptor substrate 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:20074531 10816 Irs1 insulin receptor substrate 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15467829 10816 Irs1 insulin receptor substrate 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20074531 10816 Irs1 insulin receptor substrate 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20837540 10816 Irs1 insulin receptor substrate 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7526222 10816 Irs1 insulin receptor substrate 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7969452 10816 Irs1 insulin receptor substrate 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9062343 10816 Irs1 insulin receptor substrate 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9541510 10816 Irs1 insulin receptor substrate 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18590693 10816 Irs1 insulin receptor substrate 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20837540 10816 Irs1 insulin receptor substrate 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7526222 10816 Irs1 insulin receptor substrate 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9892694 10816 Irs1 insulin receptor substrate 1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:10749573 10816 Irs1 insulin receptor substrate 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:9541510 10816 Irs1 insulin receptor substrate 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12810606 10816 Irs1 insulin receptor substrate 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9541510 10816 Irs1 insulin receptor substrate 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12810606 10816 Irs1 insulin receptor substrate 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12502742 10816 Irs1 insulin receptor substrate 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15467829 10816 Irs1 insulin receptor substrate 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:18590693 10816 Irs1 insulin receptor substrate 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12502742 10816 Irs1 insulin receptor substrate 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7969452 10816 Irs1 insulin receptor substrate 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9062343 10816 Irs1 insulin receptor substrate 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160929 MGI PMID:27534441 10816 Irs1 insulin receptor substrate 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11259600 10816 Irs1 insulin receptor substrate 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12502742 10816 Irs1 insulin receptor substrate 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7969452 10816 Irs1 insulin receptor substrate 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10749573 10816 Irs1 insulin receptor substrate 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12502742 10816 Irs1 insulin receptor substrate 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18590692 10816 Irs1 insulin receptor substrate 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18590693 10816 Irs1 insulin receptor substrate 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20074531 10816 Irs1 insulin receptor substrate 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:7526222 10816 Irs1 insulin receptor substrate 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:7969452 10816 Irs1 insulin receptor substrate 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9062343 10816 Irs1 insulin receptor substrate 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20837540 10816 Irs1 insulin receptor substrate 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20837540 10816 Irs1 insulin receptor substrate 1 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:7969452 10816 Irs1 insulin receptor substrate 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:20837540 10816 Irs1 insulin receptor substrate 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12502742 10816 Irs1 insulin receptor substrate 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18590693 10816 Irs1 insulin receptor substrate 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12502742 10816 Irs1 insulin receptor substrate 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18590693 10816 Irs1 insulin receptor substrate 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15467829 10816 Irs1 insulin receptor substrate 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:10749573 10816 Irs1 insulin receptor substrate 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20141003 MGI PMID:14736890 10816 Irs1 insulin receptor substrate 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:11078455 10816 Irs1 insulin receptor substrate 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:10749573 10816 Irs1 insulin receptor substrate 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:14736890 10816 Irs1 insulin receptor substrate 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7969452 10816 Irs1 insulin receptor substrate 1 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:18590692 10816 Irs1 insulin receptor substrate 1 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:18590693 10816 Irs1 insulin receptor substrate 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:12810606 10816 Irs1 insulin receptor substrate 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:10749573 10816 Irs1 insulin receptor substrate 1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:10749573 10816 Irs1 insulin receptor substrate 1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11259600 10816 Irs1 insulin receptor substrate 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18590693 10816 Irs1 insulin receptor substrate 1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15467829 10816 Irs1 insulin receptor substrate 1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20074531 10816 Irs1 insulin receptor substrate 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12502742 10816 Irs1 insulin receptor substrate 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18590693 10816 Irs1 insulin receptor substrate 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20074531 10816 Irs1 insulin receptor substrate 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:7526222 10816 Irs1 insulin receptor substrate 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:9062343 10816 Irs1 insulin receptor substrate 1 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12502742 10816 Irs1 insulin receptor substrate 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12502742 10816 Irs1 insulin receptor substrate 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12810606 10816 Irs1 insulin receptor substrate 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:18590692 10816 Irs1 insulin receptor substrate 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:18590693 10816 Irs1 insulin receptor substrate 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:20074531 10816 Irs1 insulin receptor substrate 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:7526222 10816 Irs1 insulin receptor substrate 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:7969452 10816 Irs1 insulin receptor substrate 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:9062343 10816 Irs1 insulin receptor substrate 1 gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:12502742 10816 Irs1 insulin receptor substrate 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12502742 10816 Irs1 insulin receptor substrate 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9062343 10816 Irs1 insulin receptor substrate 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18590693 10816 Irs1 insulin receptor substrate 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:12810606 10816 Irs1 insulin receptor substrate 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12502742 10816 Irs1 insulin receptor substrate 1 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9541510 10816 Irs1 insulin receptor substrate 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12810606 10816 Irs1 insulin receptor substrate 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9541510 10816 Irs1 insulin receptor substrate 1 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:10749573 10816 Irs1 insulin receptor substrate 1 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:9541510 10816 Irs1 insulin receptor substrate 1 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:10749573 10816 Irs1 insulin receptor substrate 1 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:12502742 10816 Irs1 insulin receptor substrate 1 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:9062343 10816 Irs1 insulin receptor substrate 1 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:7969452 10816 Irs1 insulin receptor substrate 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:7526222 10816 Irs1 insulin receptor substrate 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:20837540 10816 Irs1 insulin receptor substrate 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:14736890 10816 Irs1 insulin receptor substrate 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:18590693 10816 Irs1 insulin receptor substrate 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10816 Irs1 insulin receptor substrate 1 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20032200 10816 Irs1 insulin receptor substrate 1 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:10749573 10816 Irs1 insulin receptor substrate 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 10816 Irs1 insulin receptor substrate 1 gene MP:0030439 decreased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:20032200 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20105241 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12904471 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12904471 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20570943 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:7508365 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:20570943 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:7508365 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:7508365 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20171228 MGI PMID:28806779 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7508365 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7508365 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20570943 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:20570943 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:7508365 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:7508365 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:20570943 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20570943 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7508365 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:7508365 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:20570943 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:7508365 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:7508365 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:20105241 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0006323 abnormal extraembryonic mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:7508365 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0006325 impaired hearing IAGP N RGD:5509061 20171228 MGI PMID:28806779 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:20570943 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20570943 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0010466 vascular ring IAGP N RGD:5509061 20141003 MGI PMID:20570943 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20570943 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20570943 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7508365 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20570943 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20171228 MGI PMID:28806779 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:7508365 10817 Itga5 integrin alpha 5 (fibronectin receptor alpha) gene MP:0012183 decreased paraxial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:7508365 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0001265 decreased body size IAGP N RGD:5509061 20201001 MGI PMID:30856165 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0004092 absent Z line IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19498443 10820 Itpa inosine triphosphatase (nucleoside triphosphate pyrophosphatase) gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19498443 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:9302515 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:8538767 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:23884927 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:23884927 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8530061 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8987786 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9302515 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20170216 MGI PMID:27108798 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:8530061 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:8987786 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:23884927 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:8538767 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9302515 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20150730 MGI 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0001523 impaired righting response IEA N RGD:5509061 20111116 MGI 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0001525 impaired balance IEA N RGD:5509061 20111116 MGI 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20170105 MGI 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:23884927 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:8530061 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:8538767 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:8987786 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:9302515 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17590087 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:23884927 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0002880 opisthotonus IEA N RGD:5509061 20111116 MGI 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:8538767 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:23884927 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20150827 MGI PMID:26168218 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:9302515 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:17590087 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:8538767 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0004930 small epididymis IEA N RGD:5509061 20170105 MGI 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20150827 MGI PMID:26168218 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9302515 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0006156 abnormal visual pursuit IAGP N RGD:5509061 20141003 MGI PMID:23884927 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:23884927 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8530061 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8987786 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8538767 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8538767 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 10821 Itpr1 inositol 1,4,5-trisphosphate receptor 1 gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:23884927 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0000018 small ears IAGP N RGD:5509061 20151112 MGI PMID:26234751 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:3996911 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0000416 sparse hair IEA N RGD:5509061 20141003 MGI 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0000427 abnormal hair cycle IEA N RGD:5509061 20141003 MGI 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20151112 MGI PMID:26234751 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20151112 MGI PMID:26234751 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:16195467 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220811 MGI 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220811 MGI 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0000753 paralysis IAGP N RGD:5509061 20151112 MGI PMID:26234751 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20160512 MGI PMID:25879444 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23859941 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20160512 MGI PMID:18728777 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16195467 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16195467 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151112 MGI PMID:26234751 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0001314 cornea opacity IEA N RGD:5509061 20210520 MGI 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160512 MGI PMID:17559418 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20160512 MGI PMID:17559418 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20141003 MGI PMID:23859941 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20160512 MGI PMID:17559418 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20160512 MGI PMID:18728777 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16195467 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0001985 abnormal gustatory system physiology IAGP N RGD:5509061 20141003 MGI PMID:23859941 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:3996911 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:924142 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16195467 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20151112 MGI PMID:26234751 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16195467 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20160512 MGI PMID:25879444 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20160512 MGI PMID:25879444 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20151112 MGI PMID:26234751 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0002694 abnormal pancreas secretion IAGP N RGD:5509061 20141003 MGI PMID:16195467 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0002791 steatorrhea IAGP N RGD:5509061 20141003 MGI PMID:16195467 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0002865 increased growth rate IAGP N RGD:5509061 20160512 MGI PMID:18728777 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0002969 impaired social transmission of food preference IAGP N RGD:5509061 20160512 MGI PMID:17559418 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20160512 MGI PMID:17559418 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20141003 MGI PMID:16195467 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:16195467 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0004179 transmission ratio distortion IEA N RGD:5509061 20141003 MGI 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0005310 abnormal salivary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:16195467 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0005323 dystonia IAGP N RGD:5509061 20151112 MGI PMID:26234751 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:16195467 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16195467 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20151112 MGI PMID:26234751 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0008222 decreased hippocampal commissure size IAGP N RGD:5509061 20160512 MGI PMID:25879444 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20160512 MGI PMID:25879444 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20160609 MGI PMID:26234751 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20160512 MGI PMID:25879444 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16195467 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0009161 pancreatic acinar cell zymogen granule accumulation IAGP N RGD:5509061 20141003 MGI PMID:16195467 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20151112 MGI PMID:26234751 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0011000 abnormal allogrooming behavior IAGP N RGD:5509061 20160512 MGI PMID:17559418 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:23859941 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0012347 low sweet preference IAGP N RGD:5509061 20141003 MGI PMID:23859941 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0013140 excessive vocalization IAGP N RGD:5509061 20160512 MGI PMID:18728777 10822 Itpr3 inositol 1,4,5-triphosphate receptor 3 gene MP:0014476 abnormal feces lipid level IAGP N RGD:5509061 20240704 MGI PMID:16195467 10823 Jak2 Janus kinase 2 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20150702 MGI PMID:25552701 10823 Jak2 Janus kinase 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20211104 MGI PMID:26692333 10823 Jak2 Janus kinase 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:9590173 10823 Jak2 Janus kinase 2 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0000239 absent common myeloid progenitor cells IAGP N RGD:5509061 20141003 MGI PMID:9590174 10823 Jak2 Janus kinase 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9590173 10823 Jak2 Janus kinase 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:15169911 10823 Jak2 Janus kinase 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:16887119 10823 Jak2 Janus kinase 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:9590173 10823 Jak2 Janus kinase 2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:24169825 10823 Jak2 Janus kinase 2 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:15169911 10823 Jak2 Janus kinase 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:24086539 10823 Jak2 Janus kinase 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9590174 10823 Jak2 Janus kinase 2 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9590174 10823 Jak2 Janus kinase 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16887119 10823 Jak2 Janus kinase 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220203 MGI PMID:21209203 10823 Jak2 Janus kinase 2 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20220203 MGI PMID:21209203 10823 Jak2 Janus kinase 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220203 MGI PMID:21209203 10823 Jak2 Janus kinase 2 gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20220203 MGI PMID:21209203 10823 Jak2 Janus kinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15169911 10823 Jak2 Janus kinase 2 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20150702 MGI PMID:25552701 10823 Jak2 Janus kinase 2 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20150702 MGI PMID:25552701 10823 Jak2 Janus kinase 2 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20220203 MGI PMID:21209203 10823 Jak2 Janus kinase 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20150702 MGI PMID:25552701 10823 Jak2 Janus kinase 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20220203 MGI PMID:21209203 10823 Jak2 Janus kinase 2 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20220203 MGI PMID:21209203 10823 Jak2 Janus kinase 2 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20150702 MGI PMID:25552701 10823 Jak2 Janus kinase 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24086539 10823 Jak2 Janus kinase 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20150702 MGI PMID:25552701 10823 Jak2 Janus kinase 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20150702 MGI PMID:25552701 10823 Jak2 Janus kinase 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20220203 MGI PMID:21209203 10823 Jak2 Janus kinase 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:24169825 10823 Jak2 Janus kinase 2 gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:24169825 10823 Jak2 Janus kinase 2 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20211104 MGI PMID:26692333 10823 Jak2 Janus kinase 2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20220203 MGI PMID:21209203 10823 Jak2 Janus kinase 2 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220203 MGI PMID:21209203 10823 Jak2 Janus kinase 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20211104 MGI PMID:26692333 10823 Jak2 Janus kinase 2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0005426 tachypnea IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20211104 MGI PMID:26692333 10823 Jak2 Janus kinase 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:24086539 10823 Jak2 Janus kinase 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20150702 MGI PMID:25552701 10823 Jak2 Janus kinase 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20211104 MGI PMID:26692333 10823 Jak2 Janus kinase 2 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20150702 MGI PMID:25552701 10823 Jak2 Janus kinase 2 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20150702 MGI PMID:25552701 10823 Jak2 Janus kinase 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16887119 10823 Jak2 Janus kinase 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24169825 10823 Jak2 Janus kinase 2 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20150702 MGI PMID:25552701 10823 Jak2 Janus kinase 2 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:15169911 10823 Jak2 Janus kinase 2 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:15169911 10823 Jak2 Janus kinase 2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20150702 MGI PMID:25552701 10823 Jak2 Janus kinase 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20150702 MGI PMID:25552701 10823 Jak2 Janus kinase 2 gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24086539 10823 Jak2 Janus kinase 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20150702 MGI PMID:25552701 10823 Jak2 Janus kinase 2 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20211104 MGI PMID:26692333 10823 Jak2 Janus kinase 2 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:20472827 10823 Jak2 Janus kinase 2 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0008976 delayed female fertility IAGP N RGD:5509061 20220203 MGI PMID:21209203 10823 Jak2 Janus kinase 2 gene MP:0009008 delayed estrous cycle IAGP N RGD:5509061 20220203 MGI PMID:21209203 10823 Jak2 Janus kinase 2 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20220203 MGI PMID:21209203 10823 Jak2 Janus kinase 2 gene MP:0009015 short proestrus IAGP N RGD:5509061 20220203 MGI PMID:21209203 10823 Jak2 Janus kinase 2 gene MP:0009020 prolonged metestrus IAGP N RGD:5509061 20220203 MGI PMID:21209203 10823 Jak2 Janus kinase 2 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:15169911 10823 Jak2 Janus kinase 2 gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15169911 10823 Jak2 Janus kinase 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9590173 10823 Jak2 Janus kinase 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16887119 10823 Jak2 Janus kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24169825 10823 Jak2 Janus kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9590174 10823 Jak2 Janus kinase 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24086539 10823 Jak2 Janus kinase 2 gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0011746 spleen fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0011746 spleen fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0011747 myelofibrosis IAGP N RGD:5509061 20141003 MGI PMID:22144185 10823 Jak2 Janus kinase 2 gene MP:0011747 myelofibrosis IAGP N RGD:5509061 20141003 MGI PMID:23863895 10823 Jak2 Janus kinase 2 gene MP:0011747 myelofibrosis IAGP N RGD:5509061 20211104 MGI PMID:20489053 10823 Jak2 Janus kinase 2 gene MP:0013147 limb paralysis IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0020399 enhanced megakaryocyte emperipolesis IAGP N RGD:5509061 20170803 MGI PMID:20541703 10823 Jak2 Janus kinase 2 gene MP:0020463 increased megakaryocyte progenitor cell number IAGP N RGD:5509061 20190905 MGI PMID:29202466 10823 Jak2 Janus kinase 2 gene MP:0030025 giant platelets IAGP N RGD:5509061 20170803 MGI PMID:20472827 10824 Jak3 Janus kinase 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10419884 10824 Jak3 Janus kinase 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10419884 10824 Jak3 Janus kinase 3 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10419884 10824 Jak3 Janus kinase 3 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20111116 MGI 10824 Jak3 Janus kinase 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:10419884 10824 Jak3 Janus kinase 3 gene MP:0000493 rectal prolapse IEA N RGD:5509061 20111116 MGI 10824 Jak3 Janus kinase 3 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:10419884 10824 Jak3 Janus kinase 3 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:16878135 10824 Jak3 Janus kinase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10419884 10824 Jak3 Janus kinase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22363534 10824 Jak3 Janus kinase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:8887051 10824 Jak3 Janus kinase 3 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0000692 small spleen IAGP N RGD:5509061 20181220 MGI PMID:30372741 10824 Jak3 Janus kinase 3 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 10824 Jak3 Janus kinase 3 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:16878135 10824 Jak3 Janus kinase 3 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:22363534 10824 Jak3 Janus kinase 3 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0000706 small thymus IAGP N RGD:5509061 20181220 MGI PMID:30372741 10824 Jak3 Janus kinase 3 gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11034372 10824 Jak3 Janus kinase 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 10824 Jak3 Janus kinase 3 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20181220 MGI PMID:30372741 10824 Jak3 Janus kinase 3 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20231207 MGI 10824 Jak3 Janus kinase 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 10824 Jak3 Janus kinase 3 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 10824 Jak3 Janus kinase 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 10824 Jak3 Janus kinase 3 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10419884 10824 Jak3 Janus kinase 3 gene MP:0001606 impaired hematopoiesis IEA N RGD:5509061 20151119 MGI 10824 Jak3 Janus kinase 3 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230601 MGI 10824 Jak3 Janus kinase 3 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8887051 10824 Jak3 Janus kinase 3 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0001806 decreased IgM level IEA N RGD:5509061 20190606 MGI 10824 Jak3 Janus kinase 3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8887051 10824 Jak3 Janus kinase 3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9016869 10824 Jak3 Janus kinase 3 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:10419884 10824 Jak3 Janus kinase 3 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:9016869 10824 Jak3 Janus kinase 3 gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 10824 Jak3 Janus kinase 3 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14993294 10824 Jak3 Janus kinase 3 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11034372 10824 Jak3 Janus kinase 3 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210520 MGI 10824 Jak3 Janus kinase 3 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8887051 10824 Jak3 Janus kinase 3 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:16878135 10824 Jak3 Janus kinase 3 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:10419884 10824 Jak3 Janus kinase 3 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16020505 10824 Jak3 Janus kinase 3 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16878135 10824 Jak3 Janus kinase 3 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:22363534 10824 Jak3 Janus kinase 3 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15147562 10824 Jak3 Janus kinase 3 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9016869 10824 Jak3 Janus kinase 3 gene MP:0002497 increased IgE level IEA N RGD:5509061 20150305 MGI 10824 Jak3 Janus kinase 3 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:10419884 10824 Jak3 Janus kinase 3 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16878135 10824 Jak3 Janus kinase 3 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 10824 Jak3 Janus kinase 3 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:16878135 10824 Jak3 Janus kinase 3 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20181220 MGI PMID:30372741 10824 Jak3 Janus kinase 3 gene MP:0003304 large intestinal inflammation IEA N RGD:5509061 20111116 MGI 10824 Jak3 Janus kinase 3 gene MP:0003944 abnormal T cell subpopulation ratio IEA N RGD:5509061 20111116 MGI 10824 Jak3 Janus kinase 3 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15147562 10824 Jak3 Janus kinase 3 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20181220 MGI PMID:30372741 10824 Jak3 Janus kinase 3 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20181220 MGI PMID:30372741 10824 Jak3 Janus kinase 3 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22363534 10824 Jak3 Janus kinase 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 10824 Jak3 Janus kinase 3 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20181220 MGI PMID:30372741 10824 Jak3 Janus kinase 3 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20181220 MGI PMID:30372741 10824 Jak3 Janus kinase 3 gene MP:0004978 decreased B-1 B cell number IEA N RGD:5509061 20151119 MGI 10824 Jak3 Janus kinase 3 gene MP:0005014 increased B cell number IEA N RGD:5509061 20150305 MGI 10824 Jak3 Janus kinase 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10419884 10824 Jak3 Janus kinase 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:14993294 10824 Jak3 Janus kinase 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22363534 10824 Jak3 Janus kinase 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20111116 MGI 10824 Jak3 Janus kinase 3 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0005036 diarrhea IEA N RGD:5509061 20111116 MGI 10824 Jak3 Janus kinase 3 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8887051 10824 Jak3 Janus kinase 3 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9016869 10824 Jak3 Janus kinase 3 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20181220 MGI PMID:30372741 10824 Jak3 Janus kinase 3 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20181220 MGI PMID:30372741 10824 Jak3 Janus kinase 3 gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0005425 increased macrophage cell number IEA N RGD:5509061 20151119 MGI 10824 Jak3 Janus kinase 3 gene MP:0005461 abnormal dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16020505 10824 Jak3 Janus kinase 3 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20181220 MGI PMID:30372741 10824 Jak3 Janus kinase 3 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9016869 10824 Jak3 Janus kinase 3 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20190411 MGI 10824 Jak3 Janus kinase 3 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:22363534 10824 Jak3 Janus kinase 3 gene MP:0008046 absent NK cells IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:22363534 10824 Jak3 Janus kinase 3 gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:9016869 10824 Jak3 Janus kinase 3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22363534 10824 Jak3 Janus kinase 3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8887051 10824 Jak3 Janus kinase 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16020505 10824 Jak3 Janus kinase 3 gene MP:0008076 abnormal CD4-positive T cell differentiation IEA N RGD:5509061 20190411 MGI 10824 Jak3 Janus kinase 3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22363534 10824 Jak3 Janus kinase 3 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16020505 10824 Jak3 Janus kinase 3 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8887051 10824 Jak3 Janus kinase 3 gene MP:0008082 increased single-positive T cell number IEA N RGD:5509061 20150305 MGI 10824 Jak3 Janus kinase 3 gene MP:0008083 decreased single-positive T cell number IEA N RGD:5509061 20150305 MGI 10824 Jak3 Janus kinase 3 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16020505 10824 Jak3 Janus kinase 3 gene MP:0008121 increased myeloid dendritic cell number IEA N RGD:5509061 20151119 MGI 10824 Jak3 Janus kinase 3 gene MP:0008122 decreased myeloid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:16020505 10824 Jak3 Janus kinase 3 gene MP:0008127 decreased dendritic cell number IEA N RGD:5509061 20190606 MGI 10824 Jak3 Janus kinase 3 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20190606 MGI 10824 Jak3 Janus kinase 3 gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20190606 MGI 10824 Jak3 Janus kinase 3 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10419884 10824 Jak3 Janus kinase 3 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22363534 10824 Jak3 Janus kinase 3 gene MP:0008728 increased memory B cell number IEA N RGD:5509061 20150305 MGI 10824 Jak3 Janus kinase 3 gene MP:0008729 decreased memory B cell number IEA N RGD:5509061 20151119 MGI 10824 Jak3 Janus kinase 3 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:10419884 10824 Jak3 Janus kinase 3 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16020505 10824 Jak3 Janus kinase 3 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:7481767 10824 Jak3 Janus kinase 3 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:9016869 10824 Jak3 Janus kinase 3 gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20181220 MGI PMID:30372741 10824 Jak3 Janus kinase 3 gene MP:0009540 absent Hassall's corpuscle IAGP N RGD:5509061 20141003 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20150326 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22363534 10824 Jak3 Janus kinase 3 gene MP:0010751 decreased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22363534 10824 Jak3 Janus kinase 3 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20150305 MGI 10824 Jak3 Janus kinase 3 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20150305 MGI 10824 Jak3 Janus kinase 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 10824 Jak3 Janus kinase 3 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20181220 MGI PMID:30372741 10824 Jak3 Janus kinase 3 gene MP:0012671 retina spots IAGP N RGD:5509061 20181220 MGI PMID:30372741 10824 Jak3 Janus kinase 3 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20190606 MGI 10824 Jak3 Janus kinase 3 gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:8777722 10824 Jak3 Janus kinase 3 gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20150305 MGI 10824 Jak3 Janus kinase 3 gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20150305 MGI 10824 Jak3 Janus kinase 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 10824 Jak3 Janus kinase 3 gene MP:0020916 increased susceptibility to Herpesvirales infection IEA N RGD:5509061 20200430 MGI 10825 Espn espin gene MP:0000026 abnormal inner ear morphology IEA N RGD:5509061 20111116 MGI 10825 Espn espin gene MP:0000034 abnormal inner ear vestibule morphology IEA N RGD:5509061 20111116 MGI 10825 Espn espin gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:6871029 10825 Espn espin gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:1636414 10825 Espn espin gene MP:0000048 abnormal stria vascularis morphology IEA N RGD:5509061 20111116 MGI 10825 Espn espin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:5955164 10825 Espn espin gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:16588504 10825 Espn espin gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:5955164 10825 Espn espin gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:5955164 10825 Espn espin gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:5955164 10825 Espn espin gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:16588504 10825 Espn espin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:5955164 10825 Espn espin gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:5955164 10825 Espn espin gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:16235133 10825 Espn espin gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16588504 10825 Espn espin gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:16235133 10825 Espn espin gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:16588504 10825 Espn espin gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:5955164 10825 Espn espin gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1636414 10825 Espn espin gene MP:0002630 abnormal endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:6871029 10825 Espn espin gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:16588504 10825 Espn espin gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:5955164 10825 Espn espin gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:5955164 10825 Espn espin gene MP:0002855 abnormal cochlear ganglion morphology IEA N RGD:5509061 20111116 MGI 10825 Espn espin gene MP:0002857 cochlear ganglion degeneration IEA N RGD:5509061 20111116 MGI 10825 Espn espin gene MP:0002895 abnormal otolithic membrane morphology IEA N RGD:5509061 20111229 MGI 10825 Espn espin gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:5955164 10825 Espn espin gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:6871029 10825 Espn espin gene MP:0003150 detached tectorial membrane IEA N RGD:5509061 20111116 MGI 10825 Espn espin gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:5955164 10825 Espn espin gene MP:0003878 abnormal ear physiology IEA N RGD:5509061 20111116 MGI 10825 Espn espin gene MP:0004324 vestibular hair cell degeneration IEA N RGD:5509061 20111116 MGI 10825 Espn espin gene MP:0004331 vestibular saccular macula degeneration IEA N RGD:5509061 20111116 MGI 10825 Espn espin gene MP:0004333 abnormal utricular macula morphology IEA N RGD:5509061 20111116 MGI 10825 Espn espin gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:1636414 10825 Espn espin gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:6871029 10825 Espn espin gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:1636414 10825 Espn espin gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:6871029 10825 Espn espin gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:1636414 10825 Espn espin gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:6871029 10825 Espn espin gene MP:0004409 abnormal crista ampullaris neuroepithelium morphology IEA N RGD:5509061 20111116 MGI 10825 Espn espin gene MP:0004413 absent cochlear microphonics IAGP N RGD:5509061 20141003 MGI PMID:6871029 10825 Espn espin gene MP:0004416 absent cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:6871029 10825 Espn espin gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20240321 MGI PMID:26926603 10825 Espn espin gene MP:0004519 thin vestibular hair cell stereocilia IAGP N RGD:5509061 20240321 MGI PMID:26926603 10825 Espn espin gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:1636414 10825 Espn espin gene MP:0004523 decreased cochlear hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:16206170 10825 Espn espin gene MP:0004524 short cochlear hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:16206170 10825 Espn espin gene MP:0004525 thin cochlear hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:16206170 10825 Espn espin gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20240321 MGI PMID:26926603 10825 Espn espin gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:1636414 10825 Espn espin gene MP:0004586 pillar cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:1636414 10825 Espn espin gene MP:0004586 pillar cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:6871029 10825 Espn espin gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12209292 10825 Espn espin gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 10825 Espn espin gene MP:0004814 reduced linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 10825 Espn espin gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 10825 Espn espin gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160804 MGI 10825 Espn espin gene MP:0006335 abnormal hearing electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:6871029 10825 Espn espin gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20141003 MGI 10825 Espn espin gene MP:0008763 abnormal mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:8962054 10825 Espn espin gene MP:0010323 retropulsion IAGP N RGD:5509061 20141003 MGI PMID:16588504 10825 Espn espin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12209292 10825 Espn espin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:1636414 10828 Jun jun proto-oncogene gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12441295 10828 Jun jun proto-oncogene gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:12441295 10828 Jun jun proto-oncogene gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:8371760 10828 Jun jun proto-oncogene gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231214 MGI PMID:23437302 10828 Jun jun proto-oncogene gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11818961 10828 Jun jun proto-oncogene gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10080190 10828 Jun jun proto-oncogene gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20300111 10828 Jun jun proto-oncogene gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20201022 MGI 10828 Jun jun proto-oncogene gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:8371760 10828 Jun jun proto-oncogene gene MP:0000608 dissociated hepatocytes IAGP N RGD:5509061 20141003 MGI PMID:8371760 10828 Jun jun proto-oncogene gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 10828 Jun jun proto-oncogene gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:8371760 10828 Jun jun proto-oncogene gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:21827743 10828 Jun jun proto-oncogene gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21827743 10828 Jun jun proto-oncogene gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20300111 10828 Jun jun proto-oncogene gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:16163348 10828 Jun jun proto-oncogene gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:16163348 10828 Jun jun proto-oncogene gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:16163348 10828 Jun jun proto-oncogene gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12441295 10828 Jun jun proto-oncogene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10080190 10828 Jun jun proto-oncogene gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10080190 10828 Jun jun proto-oncogene gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11927562 10828 Jun jun proto-oncogene gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12441295 10828 Jun jun proto-oncogene gene MP:0001293 anophthalmia IEA N RGD:5509061 20201022 MGI 10828 Jun jun proto-oncogene gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:12791271 10828 Jun jun proto-oncogene gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:11818961 10828 Jun jun proto-oncogene gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:12441295 10828 Jun jun proto-oncogene gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:12791271 10828 Jun jun proto-oncogene gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:20300111 10828 Jun jun proto-oncogene gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:12791271 10828 Jun jun proto-oncogene gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 10828 Jun jun proto-oncogene gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11818961 10828 Jun jun proto-oncogene gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16163348 10828 Jun jun proto-oncogene gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:8371760 10828 Jun jun proto-oncogene gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 10828 Jun jun proto-oncogene gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:8371760 10828 Jun jun proto-oncogene gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:12791271 10828 Jun jun proto-oncogene gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16163348 10828 Jun jun proto-oncogene gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:22265050 10828 Jun jun proto-oncogene gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 10828 Jun jun proto-oncogene gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:22265050 10828 Jun jun proto-oncogene gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:16163348 10828 Jun jun proto-oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11818961 10828 Jun jun proto-oncogene gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20201022 MGI 10828 Jun jun proto-oncogene gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20300111 10828 Jun jun proto-oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10080190 10828 Jun jun proto-oncogene gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 10828 Jun jun proto-oncogene gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:10352021 10828 Jun jun proto-oncogene gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:11818961 10828 Jun jun proto-oncogene gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:20300111 10828 Jun jun proto-oncogene gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12791271 10828 Jun jun proto-oncogene gene MP:0002658 abnormal liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:11927562 10828 Jun jun proto-oncogene gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20231214 MGI PMID:23437302 10828 Jun jun proto-oncogene gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20231214 MGI PMID:23437302 10828 Jun jun proto-oncogene gene MP:0002748 abnormal pulmonary valve morphology IAGP N RGD:5509061 20231214 MGI PMID:23437302 10828 Jun jun proto-oncogene gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:10080190 10828 Jun jun proto-oncogene gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:12791271 10828 Jun jun proto-oncogene gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:8371760 10828 Jun jun proto-oncogene gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:16163348 10828 Jun jun proto-oncogene gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20935640 10828 Jun jun proto-oncogene gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12163468 10828 Jun jun proto-oncogene gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21893599 10828 Jun jun proto-oncogene gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:11927562 10828 Jun jun proto-oncogene gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:16163348 10828 Jun jun proto-oncogene gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:12791271 10828 Jun jun proto-oncogene gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:20300111 10828 Jun jun proto-oncogene gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16163348 10828 Jun jun proto-oncogene gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10352021 10828 Jun jun proto-oncogene gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8371760 10828 Jun jun proto-oncogene gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20300111 10828 Jun jun proto-oncogene gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:10352021 10828 Jun jun proto-oncogene gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:10352021 10828 Jun jun proto-oncogene gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20231214 MGI PMID:23437302 10828 Jun jun proto-oncogene gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:12441295 10828 Jun jun proto-oncogene gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:12441295 10828 Jun jun proto-oncogene gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:16163348 10828 Jun jun proto-oncogene gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20141003 MGI PMID:20935640 10828 Jun jun proto-oncogene gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231214 MGI PMID:23437302 10828 Jun jun proto-oncogene gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20300111 10828 Jun jun proto-oncogene gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:10080190 10828 Jun jun proto-oncogene gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:10080190 10828 Jun jun proto-oncogene gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:22265050 10828 Jun jun proto-oncogene gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22265050 10828 Jun jun proto-oncogene gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20210128 MGI 10828 Jun jun proto-oncogene gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:11818961 10828 Jun jun proto-oncogene gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:12791271 10828 Jun jun proto-oncogene gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20141003 MGI PMID:21827743 10828 Jun jun proto-oncogene gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8371760 10828 Jun jun proto-oncogene gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12791271 10828 Jun jun proto-oncogene gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20141003 MGI PMID:12791271 10828 Jun jun proto-oncogene gene MP:0009859 eye opacity IAGP N RGD:5509061 20141003 MGI PMID:12791271 10828 Jun jun proto-oncogene gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:10352021 10828 Jun jun proto-oncogene gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11818961 10828 Jun jun proto-oncogene gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231214 MGI PMID:23437302 10828 Jun jun proto-oncogene gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20231214 MGI PMID:23437302 10828 Jun jun proto-oncogene gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:11818961 10828 Jun jun proto-oncogene gene MP:0010602 abnormal pulmonary valve cusp morphology IAGP N RGD:5509061 20231214 MGI PMID:23437302 10828 Jun jun proto-oncogene gene MP:0010605 thick pulmonary valve cusps IAGP N RGD:5509061 20231214 MGI PMID:23437302 10828 Jun jun proto-oncogene gene MP:0010617 thick mitral valve cusps IAGP N RGD:5509061 20231214 MGI PMID:23437302 10828 Jun jun proto-oncogene gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20141003 MGI PMID:22265050 10828 Jun jun proto-oncogene gene MP:0010901 abnormal pulmonary alveolar parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:22265050 10828 Jun jun proto-oncogene gene MP:0010971 abnormal periosteum morphology IAGP N RGD:5509061 20141003 MGI PMID:16163348 10828 Jun jun proto-oncogene gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11818961 10828 Jun jun proto-oncogene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11818961 10828 Jun jun proto-oncogene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12441295 10828 Jun jun proto-oncogene gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20300111 10828 Jun jun proto-oncogene gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11818961 10828 Jun jun proto-oncogene gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11818961 10828 Jun jun proto-oncogene gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20300111 10828 Jun jun proto-oncogene gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8330736 10828 Jun jun proto-oncogene gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11818961 10828 Jun jun proto-oncogene gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8371760 10828 Jun jun proto-oncogene gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10828 Jun jun proto-oncogene gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12441295 10828 Jun jun proto-oncogene gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20300111 10828 Jun jun proto-oncogene gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8371760 10828 Jun jun proto-oncogene gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:23437302 10828 Jun jun proto-oncogene gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20300111 10828 Jun jun proto-oncogene gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:8330736 10828 Jun jun proto-oncogene gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:10352021 10828 Jun jun proto-oncogene gene MP:0021160 decreased heart right ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:10352021 10828 Jun jun proto-oncogene gene MP:0030002 increased lung apoptosis IAGP N RGD:5509061 20200917 MGI PMID:22265050 10828 Jun jun proto-oncogene gene MP:0031524 mitral valve hyperplasia IAGP N RGD:5509061 20240104 MGI PMID:23437302 10828 Jun jun proto-oncogene gene MP:0031526 thin right ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:23437302 10828 Jun jun proto-oncogene gene MP:0031529 pulmonary valve hyperplasia IAGP N RGD:5509061 20240104 MGI PMID:23437302 10828 Jun jun proto-oncogene gene MP:0031581 semilunar valve hyperplasia IAGP N RGD:5509061 20240125 MGI PMID:23437302 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17634333 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17925011 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:17925011 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:17634333 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:17925011 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17634333 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:17634333 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:17634333 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:17634333 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:17634333 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:17925011 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:17634333 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20240523 MGI 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0010540 long stride length IAGP N RGD:5509061 20141003 MGI PMID:20696761 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17634333 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17925011 10830 Kcna2 potassium voltage-gated channel, shaker-related subfamily, member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 10831 Kcna4 potassium voltage-gated channel, shaker-related subfamily, member 4 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:9547391 10832 Kcna5 potassium voltage-gated channel, shaker-related subfamily, member 5 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17055293 10832 Kcna5 potassium voltage-gated channel, shaker-related subfamily, member 5 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17055293 10832 Kcna5 potassium voltage-gated channel, shaker-related subfamily, member 5 gene MP:0001200 thick skin IEA N RGD:5509061 20210520 MGI 10832 Kcna5 potassium voltage-gated channel, shaker-related subfamily, member 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 10832 Kcna5 potassium voltage-gated channel, shaker-related subfamily, member 5 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17055293 10832 Kcna5 potassium voltage-gated channel, shaker-related subfamily, member 5 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:11481235 10832 Kcna5 potassium voltage-gated channel, shaker-related subfamily, member 5 gene MP:0003488 decreased channel response intensity IAGP N RGD:5509061 20141003 MGI PMID:17055293 10832 Kcna5 potassium voltage-gated channel, shaker-related subfamily, member 5 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17055293 10832 Kcna5 potassium voltage-gated channel, shaker-related subfamily, member 5 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11481235 10832 Kcna5 potassium voltage-gated channel, shaker-related subfamily, member 5 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11349004 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:11517255 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11517255 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11517255 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11517255 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11517255 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11517255 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11517255 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:11517255 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11517255 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230601 MGI 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:11517255 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:11517255 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11517255 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:11517255 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11517255 10833 Kcnc1 potassium voltage gated channel, Shaw-related subfamily, member 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:11517255 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:11223304 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0000044 absent organ of Corti IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0000745 tremors IEA N RGD:5509061 20200514 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20201022 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201231 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:16235133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001396 unidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20200514 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:11438691 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001454 abnormal cued conditioning behavior IEA N RGD:5509061 20211021 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200514 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001512 trunk curl IEA N RGD:5509061 20200514 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:16235133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:11438691 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:16235133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20200514 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11438691 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:11438691 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20200514 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200514 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:11438691 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0003169 abnormal scala media morphology IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:11438691 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0003349 abnormal circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:11438691 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:11438691 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0003878 abnormal ear physiology IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200514 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004114 abnormal atrioventricular node morphology IAGP N RGD:5509061 20221006 MGI PMID:34459252 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004117 abnormal atrioventricular bundle morphology IAGP N RGD:5509061 20221006 MGI PMID:34459252 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004119 hypokalemia IAGP N RGD:5509061 20141003 MGI PMID:11438691 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:9933245 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11223304 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004331 vestibular saccular macula degeneration IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004334 utricular macular degeneration IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004397 absent cochlear inner hair cells IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004403 absent cochlear outer hair cells IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004409 abnormal crista ampullaris neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11223304 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004530 absent outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20111116 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004775 abnormal vestibular dark cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11223304 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004775 abnormal vestibular dark cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11438691 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004776 vestibular dark cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11438691 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004845 absent vestibuloocular reflex IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20200514 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0005633 increased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:11438691 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:15243133 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:8982171 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0008308 small scala media IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:11438691 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200514 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11003695 10834 Kcne1 potassium voltage-gated channel, Isk-related subfamily, member 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0000231 hypertension IAGP N RGD:5509061 20181122 MGI PMID:23974906 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0001263 weight loss IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0001596 hypotension IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:11984590 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:18026101 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11984590 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0002083 premature death IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:11984590 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20181122 MGI PMID:23974906 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:18026101 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18026101 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0010575 aortic arch dilation IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20200220 MGI PMID:30089727 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:16688530 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:18026101 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:16688530 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:18026101 10835 Kcnj8 potassium inwardly-rectifying channel, subfamily J, member 8 gene MP:0031192 coronary artery spasm IAGP N RGD:5509061 20201119 MGI PMID:11984590 10836 Kdr kinase insert domain protein receptor gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:20065093 10836 Kdr kinase insert domain protein receptor gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:21606590 10836 Kdr kinase insert domain protein receptor gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:23178125 10836 Kdr kinase insert domain protein receptor gene MP:0000263 absent organized vascular network IAGP N RGD:5509061 20141003 MGI PMID:15601855 10836 Kdr kinase insert domain protein receptor gene MP:0000263 absent organized vascular network IAGP N RGD:5509061 20141003 MGI PMID:15644447 10836 Kdr kinase insert domain protein receptor gene MP:0000263 absent organized vascular network IAGP N RGD:5509061 20141003 MGI PMID:7596435 10836 Kdr kinase insert domain protein receptor gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:21606590 10836 Kdr kinase insert domain protein receptor gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:23178125 10836 Kdr kinase insert domain protein receptor gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:15944181 10836 Kdr kinase insert domain protein receptor gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20170928 MGI PMID:21305688 10836 Kdr kinase insert domain protein receptor gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:23023706 10836 Kdr kinase insert domain protein receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23178125 10836 Kdr kinase insert domain protein receptor gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20160211 MGI PMID:25417109 10836 Kdr kinase insert domain protein receptor gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:19668192 10836 Kdr kinase insert domain protein receptor gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15644447 10836 Kdr kinase insert domain protein receptor gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20010698 10836 Kdr kinase insert domain protein receptor gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:19023080 10836 Kdr kinase insert domain protein receptor gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:21396893 10836 Kdr kinase insert domain protein receptor gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:23023706 10836 Kdr kinase insert domain protein receptor gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20170928 MGI PMID:21305688 10836 Kdr kinase insert domain protein receptor gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:19644017 10836 Kdr kinase insert domain protein receptor gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:19668192 10836 Kdr kinase insert domain protein receptor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21606590 10836 Kdr kinase insert domain protein receptor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7596435 10836 Kdr kinase insert domain protein receptor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170928 MGI PMID:21305688 10836 Kdr kinase insert domain protein receptor gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:15644447 10836 Kdr kinase insert domain protein receptor gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:7596435 10836 Kdr kinase insert domain protein receptor gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20141003 MGI PMID:15644447 10836 Kdr kinase insert domain protein receptor gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20141003 MGI PMID:7596435 10836 Kdr kinase insert domain protein receptor gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:16514057 10836 Kdr kinase insert domain protein receptor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19668192 10836 Kdr kinase insert domain protein receptor gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19023080 10836 Kdr kinase insert domain protein receptor gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15601855 10836 Kdr kinase insert domain protein receptor gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7596435 10836 Kdr kinase insert domain protein receptor gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:20010698 10836 Kdr kinase insert domain protein receptor gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7596435 10836 Kdr kinase insert domain protein receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15644447 10836 Kdr kinase insert domain protein receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 10836 Kdr kinase insert domain protein receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7596435 10836 Kdr kinase insert domain protein receptor gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20160211 MGI PMID:25417109 10836 Kdr kinase insert domain protein receptor gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0003543 abnormal vascular endothelial cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15601855 10836 Kdr kinase insert domain protein receptor gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:15601855 10836 Kdr kinase insert domain protein receptor gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:20010698 10836 Kdr kinase insert domain protein receptor gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20170928 MGI PMID:21305688 10836 Kdr kinase insert domain protein receptor gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:21396893 10836 Kdr kinase insert domain protein receptor gene MP:0004106 lymphatic vessel hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19668192 10836 Kdr kinase insert domain protein receptor gene MP:0004106 lymphatic vessel hyperplasia IAGP N RGD:5509061 20160211 MGI PMID:25417109 10836 Kdr kinase insert domain protein receptor gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23178125 10836 Kdr kinase insert domain protein receptor gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:20010698 10836 Kdr kinase insert domain protein receptor gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:19668192 10836 Kdr kinase insert domain protein receptor gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15644447 10836 Kdr kinase insert domain protein receptor gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21606590 10836 Kdr kinase insert domain protein receptor gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:19668192 10836 Kdr kinase insert domain protein receptor gene MP:0005167 abnormal blood-brain barrier function IAGP N RGD:5509061 20141003 MGI PMID:19023080 10836 Kdr kinase insert domain protein receptor gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:22753193 10836 Kdr kinase insert domain protein receptor gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:20010698 10836 Kdr kinase insert domain protein receptor gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19023080 10836 Kdr kinase insert domain protein receptor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:7596435 10836 Kdr kinase insert domain protein receptor gene MP:0006323 abnormal extraembryonic mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:15644447 10836 Kdr kinase insert domain protein receptor gene MP:0006338 abnormal second pharyngeal arch morphology IAGP N RGD:5509061 20170928 MGI PMID:21305688 10836 Kdr kinase insert domain protein receptor gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20160211 MGI PMID:25417109 10836 Kdr kinase insert domain protein receptor gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19668192 10836 Kdr kinase insert domain protein receptor gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22987638 10836 Kdr kinase insert domain protein receptor gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20170928 MGI PMID:21305688 10836 Kdr kinase insert domain protein receptor gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:21505259 10836 Kdr kinase insert domain protein receptor gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23178125 10836 Kdr kinase insert domain protein receptor gene MP:0010196 abnormal lymphatic vessel smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:20439428 10836 Kdr kinase insert domain protein receptor gene MP:0010200 enlarged lymphatic vessel IAGP N RGD:5509061 20141003 MGI PMID:20439428 10836 Kdr kinase insert domain protein receptor gene MP:0010200 enlarged lymphatic vessel IAGP N RGD:5509061 20160211 MGI PMID:25417109 10836 Kdr kinase insert domain protein receptor gene MP:0010642 absent third pharyngeal arch IAGP N RGD:5509061 20170928 MGI PMID:21305688 10836 Kdr kinase insert domain protein receptor gene MP:0010643 absent fourth pharyngeal arch IAGP N RGD:5509061 20170928 MGI PMID:21305688 10836 Kdr kinase insert domain protein receptor gene MP:0010939 abnormal mandibular prominence morphology IAGP N RGD:5509061 20170928 MGI PMID:21305688 10836 Kdr kinase insert domain protein receptor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20065093 10836 Kdr kinase insert domain protein receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15644447 10836 Kdr kinase insert domain protein receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16887829 10836 Kdr kinase insert domain protein receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19023080 10836 Kdr kinase insert domain protein receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21606590 10836 Kdr kinase insert domain protein receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7596435 10836 Kdr kinase insert domain protein receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170928 MGI PMID:21305688 10836 Kdr kinase insert domain protein receptor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23178125 10836 Kdr kinase insert domain protein receptor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15601855 10836 Kdr kinase insert domain protein receptor gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20160211 MGI PMID:25417109 10836 Kdr kinase insert domain protein receptor gene MP:0012756 impaired cranial neural crest cell differentiation IAGP N RGD:5509061 20170928 MGI PMID:21305688 10836 Kdr kinase insert domain protein receptor gene MP:0012757 abnormal cranial neural crest cell migration IAGP N RGD:5509061 20170928 MGI PMID:21305688 10836 Kdr kinase insert domain protein receptor gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:7596435 10838 Zfp354a zinc finger protein 354A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 10838 Zfp354a zinc finger protein 354A gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 10838 Zfp354a zinc finger protein 354A gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 10838 Zfp354a zinc finger protein 354A gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 10838 Zfp354a zinc finger protein 354A gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 10838 Zfp354a zinc finger protein 354A gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 10838 Zfp354a zinc finger protein 354A gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230119 MGI 10838 Zfp354a zinc finger protein 354A gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230119 MGI 10838 Zfp354a zinc finger protein 354A gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20231207 MGI 10843 Klkb1 kallikrein B, plasma 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201022 MGI 10843 Klkb1 kallikrein B, plasma 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201231 MGI 10843 Klkb1 kallikrein B, plasma 1 gene MP:0008817 hematoma IAGP N RGD:5509061 20141003 MGI PMID:21258336 10843 Klkb1 kallikrein B, plasma 1 gene MP:0012359 increased partial thromboplastin time IAGP N RGD:5509061 20141003 MGI PMID:21258336 10850 L1cam L1 cell adhesion molecule gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20141003 MGI PMID:11164829 10850 L1cam L1 cell adhesion molecule gene MP:0000583 long toenails IAGP N RGD:5509061 20141003 MGI PMID:9427628 10850 L1cam L1 cell adhesion molecule gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:9427628 10850 L1cam L1 cell adhesion molecule gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:11164829 10850 L1cam L1 cell adhesion molecule gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11164829 10850 L1cam L1 cell adhesion molecule gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:9580664 10850 L1cam L1 cell adhesion molecule gene MP:0000828 abnormal fourth ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9580664 10850 L1cam L1 cell adhesion molecule gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:9580664 10850 L1cam L1 cell adhesion molecule gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:11564762 10850 L1cam L1 cell adhesion molecule gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:11564762 10850 L1cam L1 cell adhesion molecule gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:11564762 10850 L1cam L1 cell adhesion molecule gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9580664 10850 L1cam L1 cell adhesion molecule gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11564762 10850 L1cam L1 cell adhesion molecule gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11564762 10850 L1cam L1 cell adhesion molecule gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:18550718 10850 L1cam L1 cell adhesion molecule gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9354804 10850 L1cam L1 cell adhesion molecule gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11564762 10850 L1cam L1 cell adhesion molecule gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9580664 10850 L1cam L1 cell adhesion molecule gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11164829 10850 L1cam L1 cell adhesion molecule gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9354804 10850 L1cam L1 cell adhesion molecule gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9427628 10850 L1cam L1 cell adhesion molecule gene MP:0001349 excessive tearing IAGP N RGD:5509061 20141003 MGI PMID:9427628 10850 L1cam L1 cell adhesion molecule gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160512 MGI PMID:26079769 10850 L1cam L1 cell adhesion molecule gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:14614101 10850 L1cam L1 cell adhesion molecule gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:14614101 10850 L1cam L1 cell adhesion molecule gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9580664 10850 L1cam L1 cell adhesion molecule gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20127821 10850 L1cam L1 cell adhesion molecule gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9580664 10850 L1cam L1 cell adhesion molecule gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:14614101 10850 L1cam L1 cell adhesion molecule gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20160512 MGI PMID:26079769 10850 L1cam L1 cell adhesion molecule gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:14614101 10850 L1cam L1 cell adhesion molecule gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:9580664 10850 L1cam L1 cell adhesion molecule gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:9354804 10850 L1cam L1 cell adhesion molecule gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:11164829 10850 L1cam L1 cell adhesion molecule gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:15067019 10850 L1cam L1 cell adhesion molecule gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9427628 10850 L1cam L1 cell adhesion molecule gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:9354804 10850 L1cam L1 cell adhesion molecule gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:9427628 10850 L1cam L1 cell adhesion molecule gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9427628 10850 L1cam L1 cell adhesion molecule gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11564762 10850 L1cam L1 cell adhesion molecule gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9580664 10850 L1cam L1 cell adhesion molecule gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:14614101 10850 L1cam L1 cell adhesion molecule gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:9580664 10850 L1cam L1 cell adhesion molecule gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:14614101 10850 L1cam L1 cell adhesion molecule gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20141003 MGI PMID:9354804 10850 L1cam L1 cell adhesion molecule gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:9580664 10850 L1cam L1 cell adhesion molecule gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:9427628 10850 L1cam L1 cell adhesion molecule gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9354804 10850 L1cam L1 cell adhesion molecule gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:18171935 10850 L1cam L1 cell adhesion molecule gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:9427628 10850 L1cam L1 cell adhesion molecule gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:9580664 10850 L1cam L1 cell adhesion molecule gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11564762 10850 L1cam L1 cell adhesion molecule gene MP:0005316 abnormal response to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:9354804 10850 L1cam L1 cell adhesion molecule gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20211118 MGI PMID:18171935 10850 L1cam L1 cell adhesion molecule gene MP:0005423 abnormal somatic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18550718 10850 L1cam L1 cell adhesion molecule gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:11164829 10850 L1cam L1 cell adhesion molecule gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:9580664 10850 L1cam L1 cell adhesion molecule gene MP:0006198 enophthalmos IAGP N RGD:5509061 20141003 MGI PMID:9354804 10850 L1cam L1 cell adhesion molecule gene MP:0006198 enophthalmos IAGP N RGD:5509061 20141003 MGI PMID:9427628 10850 L1cam L1 cell adhesion molecule gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:11164829 10850 L1cam L1 cell adhesion molecule gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:18550718 10850 L1cam L1 cell adhesion molecule gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18171935 10850 L1cam L1 cell adhesion molecule gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:20127821 10850 L1cam L1 cell adhesion molecule gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:9427628 10850 L1cam L1 cell adhesion molecule gene MP:0008534 enlarged fourth ventricle IAGP N RGD:5509061 20141003 MGI PMID:9580664 10850 L1cam L1 cell adhesion molecule gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:9354804 10850 L1cam L1 cell adhesion molecule gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15067019 10850 L1cam L1 cell adhesion molecule gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11564762 10850 L1cam L1 cell adhesion molecule gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15067019 10850 L1cam L1 cell adhesion molecule gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9427628 10850 L1cam L1 cell adhesion molecule gene MP:0011275 abnormal behavioral response to light IAGP N RGD:5509061 20160512 MGI PMID:26079769 10850 L1cam L1 cell adhesion molecule gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:11164829 10850 L1cam L1 cell adhesion molecule gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:9354804 10850 L1cam L1 cell adhesion molecule gene MP:0012484 decreased corticospinal tract size IAGP N RGD:5509061 20141003 MGI PMID:9354804 10850 L1cam L1 cell adhesion molecule gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:11164829 10853 Lalba lactalbumin, alpha gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8022817 10853 Lalba lactalbumin, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7708733 10853 Lalba lactalbumin, alpha gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:7708733 10853 Lalba lactalbumin, alpha gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:8022817 10854 Lamb2 laminin, beta 2 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:10531444 10854 Lamb2 laminin, beta 2 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10531444 10854 Lamb2 laminin, beta 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:7885444 10854 Lamb2 laminin, beta 2 gene MP:0001054 failure of neuromuscular synapse presynaptic differentiation IAGP N RGD:5509061 20141003 MGI PMID:7885444 10854 Lamb2 laminin, beta 2 gene MP:0001055 failure of neuromuscular synapse postsynaptic differentiation IAGP N RGD:5509061 20141003 MGI PMID:7885444 10854 Lamb2 laminin, beta 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24293254 10854 Lamb2 laminin, beta 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:10531444 10854 Lamb2 laminin, beta 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17711601 10854 Lamb2 laminin, beta 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:24293254 10854 Lamb2 laminin, beta 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7670489 10854 Lamb2 laminin, beta 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7885444 10854 Lamb2 laminin, beta 2 gene MP:0002083 premature death IAGP N RGD:5509061 20191212 MGI PMID:29263159 10854 Lamb2 laminin, beta 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:24293254 10854 Lamb2 laminin, beta 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20191212 MGI PMID:29263159 10854 Lamb2 laminin, beta 2 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:24293254 10854 Lamb2 laminin, beta 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:7885444 10854 Lamb2 laminin, beta 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:7670489 10854 Lamb2 laminin, beta 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20191212 MGI PMID:29263159 10854 Lamb2 laminin, beta 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:24293254 10854 Lamb2 laminin, beta 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:7670489 10854 Lamb2 laminin, beta 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:7885444 10854 Lamb2 laminin, beta 2 gene MP:0003606 kidney failure IAGP N RGD:5509061 20191212 MGI PMID:29263159 10854 Lamb2 laminin, beta 2 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10531444 10854 Lamb2 laminin, beta 2 gene MP:0004793 abnormal synaptic vesicle clustering IAGP N RGD:5509061 20141003 MGI PMID:17418794 10854 Lamb2 laminin, beta 2 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:7885444 10854 Lamb2 laminin, beta 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:24293254 10854 Lamb2 laminin, beta 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:10531444 10854 Lamb2 laminin, beta 2 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17711601 10854 Lamb2 laminin, beta 2 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:17711601 10854 Lamb2 laminin, beta 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20191212 MGI PMID:29263159 10854 Lamb2 laminin, beta 2 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:24293254 10854 Lamb2 laminin, beta 2 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17711601 10854 Lamb2 laminin, beta 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10531444 10854 Lamb2 laminin, beta 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20191212 MGI PMID:29263159 10854 Lamb2 laminin, beta 2 gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:24293254 10854 Lamb2 laminin, beta 2 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:17711601 10854 Lamb2 laminin, beta 2 gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:7885444 10854 Lamb2 laminin, beta 2 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20191212 MGI PMID:29263159 10854 Lamb2 laminin, beta 2 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:10531444 10854 Lamb2 laminin, beta 2 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:10531444 10854 Lamb2 laminin, beta 2 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24293254 10854 Lamb2 laminin, beta 2 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:17711601 10854 Lamb2 laminin, beta 2 gene MP:0010235 abnormal retina inner limiting membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17711601 10854 Lamb2 laminin, beta 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7885444 10854 Lamb2 laminin, beta 2 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:7670489 10854 Lamb2 laminin, beta 2 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20191212 MGI PMID:29263159 10854 Lamb2 laminin, beta 2 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:24293254 10854 Lamb2 laminin, beta 2 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:7670489 10854 Lamb2 laminin, beta 2 gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20191212 MGI PMID:29263159 10854 Lamb2 laminin, beta 2 gene MP:0011856 abnormal glomerular filtration barrier function IAGP N RGD:5509061 20141003 MGI PMID:7670489 10854 Lamb2 laminin, beta 2 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:10531444 10854 Lamb2 laminin, beta 2 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:10531444 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:15121881 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:15121881 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:15121881 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:15121881 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:15121881 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:15121881 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10212251 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0002188 small heart IEA N RGD:5509061 20210826 MGI 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:15121881 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:15121881 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15121881 10855 Lamp1 lysosomal-associated membrane protein 1 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:15121881 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:15121881 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:15121881 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:15121881 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:15121881 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:15121881 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0000603 pale liver IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:10972293 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10972293 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:15121881 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20181220 MGI PMID:28526246 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10972293 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10972293 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:15121881 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:10972293 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0003325 decreased liver function IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0003927 increased cellular glucose import IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0004114 abnormal atrioventricular node morphology IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0004117 abnormal atrioventricular bundle morphology IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20181220 MGI PMID:28526246 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20181220 MGI PMID:28526246 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:15121881 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10972293 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:10972293 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10972293 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20181220 MGI PMID:28526246 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:10972293 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0009122 decreased white fat cell lipid droplet size IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20181220 MGI PMID:28526246 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15121881 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:15121881 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20181220 MGI PMID:28526246 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20221006 MGI PMID:34459252 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0020103 decreased hepatic glucose production IAGP N RGD:5509061 20151112 MGI PMID:25043815 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:28526246 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20231109 MGI PMID:28526246 10857 Lamp2 lysosomal-associated membrane protein 2 gene MP:0031078 increased circulating troponin T level IAGP N RGD:5509061 20221006 MGI PMID:34459252 10858 Anpep alanyl aminopeptidase, membrane gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210520 MGI 10858 Anpep alanyl aminopeptidase, membrane gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20430777 10858 Anpep alanyl aminopeptidase, membrane gene MP:0003711 pathological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:17360568 10858 Anpep alanyl aminopeptidase, membrane gene MP:0005544 cornea deposits IEA N RGD:5509061 20210520 MGI 10858 Anpep alanyl aminopeptidase, membrane gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20210520 MGI 10858 Anpep alanyl aminopeptidase, membrane gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20430777 10858 Anpep alanyl aminopeptidase, membrane gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:17360568 10858 Anpep alanyl aminopeptidase, membrane gene MP:0012075 impaired mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:22983824 10859 Lcat lecithin cholesterol acyltransferase gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14668345 10859 Lcat lecithin cholesterol acyltransferase gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11278414 10859 Lcat lecithin cholesterol acyltransferase gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11893779 10859 Lcat lecithin cholesterol acyltransferase gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14668345 10859 Lcat lecithin cholesterol acyltransferase gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9054454 10859 Lcat lecithin cholesterol acyltransferase gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9188474 10859 Lcat lecithin cholesterol acyltransferase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9188474 10859 Lcat lecithin cholesterol acyltransferase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:11278414 10859 Lcat lecithin cholesterol acyltransferase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:9054454 10859 Lcat lecithin cholesterol acyltransferase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:9188474 10859 Lcat lecithin cholesterol acyltransferase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11278414 10859 Lcat lecithin cholesterol acyltransferase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11893779 10859 Lcat lecithin cholesterol acyltransferase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14668345 10859 Lcat lecithin cholesterol acyltransferase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9054454 10859 Lcat lecithin cholesterol acyltransferase gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:11278414 10859 Lcat lecithin cholesterol acyltransferase gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11893779 10859 Lcat lecithin cholesterol acyltransferase gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14668345 10859 Lcat lecithin cholesterol acyltransferase gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9188474 10859 Lcat lecithin cholesterol acyltransferase gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:11278414 10859 Lcat lecithin cholesterol acyltransferase gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14668345 10859 Lcat lecithin cholesterol acyltransferase gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11278414 10859 Lcat lecithin cholesterol acyltransferase gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9188474 10859 Lcat lecithin cholesterol acyltransferase gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9188474 10859 Lcat lecithin cholesterol acyltransferase gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11893779 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14668345 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11278414 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11893779 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11278414 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9054454 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9188474 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11278414 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11893779 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14668345 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9054454 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11278414 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:11893779 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:9188474 10859 Lcat lecithin cholesterol acyltransferase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:14668345 10859 Lcat lecithin cholesterol acyltransferase gene MP:0006084 abnormal circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:11278414 10859 Lcat lecithin cholesterol acyltransferase gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0011312 abnormal kidney afferent arteriole morphology IAGP N RGD:5509061 20141003 MGI PMID:11278414 10859 Lcat lecithin cholesterol acyltransferase gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:11278414 10859 Lcat lecithin cholesterol acyltransferase gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:11278414 10859 Lcat lecithin cholesterol acyltransferase gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:15466392 10859 Lcat lecithin cholesterol acyltransferase gene MP:0011579 decreased lipoprotein lipase activity IAGP N RGD:5509061 20141003 MGI PMID:14668345 10859 Lcat lecithin cholesterol acyltransferase gene MP:0031084 decreased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:11278414 10863 Ldhb lactate dehydrogenase B gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20181227 MGI 10864 Ldlr low density lipoprotein receptor gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16835442 10864 Ldlr low density lipoprotein receptor gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18410513 10864 Ldlr low density lipoprotein receptor gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11445560 10864 Ldlr low density lipoprotein receptor gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16127462 10864 Ldlr low density lipoprotein receptor gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9598833 10864 Ldlr low density lipoprotein receptor gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 10864 Ldlr low density lipoprotein receptor gene MP:0000181 abnormal circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12746448 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11138930 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11445560 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12746448 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15472122 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15840700 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16236385 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16368783 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16434491 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17080197 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17478727 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18160655 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18666258 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18820241 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21606463 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8994037 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9449704 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9701246 10864 Ldlr low density lipoprotein receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 10864 Ldlr low density lipoprotein receptor gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12639996 10864 Ldlr low density lipoprotein receptor gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14668345 10864 Ldlr low density lipoprotein receptor gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14739216 10864 Ldlr low density lipoprotein receptor gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15596719 10864 Ldlr low density lipoprotein receptor gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16873689 10864 Ldlr low density lipoprotein receptor gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18820241 10864 Ldlr low density lipoprotein receptor gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21149301 10864 Ldlr low density lipoprotein receptor gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20150101 MGI PMID:25176150 10864 Ldlr low density lipoprotein receptor gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20240425 MGI PMID:38417553 10864 Ldlr low density lipoprotein receptor gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11076954 10864 Ldlr low density lipoprotein receptor gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11893779 10864 Ldlr low density lipoprotein receptor gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14668345 10864 Ldlr low density lipoprotein receptor gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16873689 10864 Ldlr low density lipoprotein receptor gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17478727 10864 Ldlr low density lipoprotein receptor gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8994037 10864 Ldlr low density lipoprotein receptor gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 10864 Ldlr low density lipoprotein receptor gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11375415 10864 Ldlr low density lipoprotein receptor gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11375415 10864 Ldlr low density lipoprotein receptor gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11375415 10864 Ldlr low density lipoprotein receptor gene MP:0000231 hypertension IAGP N RGD:5509061 20170209 MGI PMID:18160459 10864 Ldlr low density lipoprotein receptor gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:15031124 10864 Ldlr low density lipoprotein receptor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:16236385 10864 Ldlr low density lipoprotein receptor gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:16150825 10864 Ldlr low density lipoprotein receptor gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:11530237 10864 Ldlr low density lipoprotein receptor gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:17720268 10864 Ldlr low density lipoprotein receptor gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10727439 10864 Ldlr low density lipoprotein receptor gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:11530237 10864 Ldlr low density lipoprotein receptor gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11530237 10864 Ldlr low density lipoprotein receptor gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18410513 10864 Ldlr low density lipoprotein receptor gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:10727439 10864 Ldlr low density lipoprotein receptor gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:10727439 10864 Ldlr low density lipoprotein receptor gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10727439 10864 Ldlr low density lipoprotein receptor gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16211093 10864 Ldlr low density lipoprotein receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18250194 10864 Ldlr low density lipoprotein receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:21690266 10864 Ldlr low density lipoprotein receptor gene MP:0001261 obese IAGP N RGD:5509061 20170209 MGI PMID:18160459 10864 Ldlr low density lipoprotein receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21606463 10864 Ldlr low density lipoprotein receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240425 MGI PMID:38417553 10864 Ldlr low density lipoprotein receptor gene MP:0001337 dry eyes IAGP N RGD:5509061 20141003 MGI PMID:10777503 10864 Ldlr low density lipoprotein receptor gene MP:0001345 Meibomian gland atrophy IAGP N RGD:5509061 20141003 MGI PMID:10777503 10864 Ldlr low density lipoprotein receptor gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16236385 10864 Ldlr low density lipoprotein receptor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16236385 10864 Ldlr low density lipoprotein receptor gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 10864 Ldlr low density lipoprotein receptor gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:16236385 10864 Ldlr low density lipoprotein receptor gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15207278 10864 Ldlr low density lipoprotein receptor gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16236385 10864 Ldlr low density lipoprotein receptor gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16835442 10864 Ldlr low density lipoprotein receptor gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:18466986 10864 Ldlr low density lipoprotein receptor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:16368783 10864 Ldlr low density lipoprotein receptor gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:7538675 10864 Ldlr low density lipoprotein receptor gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:11445560 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11445560 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11893779 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11983917 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12969990 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14668345 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15840700 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18410513 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18820241 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21149301 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21606463 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21690266 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:7538675 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:8941642 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:8994037 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9449704 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9598833 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9701246 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9734366 10864 Ldlr low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170209 MGI PMID:18160459 10864 Ldlr low density lipoprotein receptor gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21690266 10864 Ldlr low density lipoprotein receptor gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20170209 MGI PMID:18160459 10864 Ldlr low density lipoprotein receptor gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11445560 10864 Ldlr low density lipoprotein receptor gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15840700 10864 Ldlr low density lipoprotein receptor gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16368783 10864 Ldlr low density lipoprotein receptor gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18820241 10864 Ldlr low density lipoprotein receptor gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21606463 10864 Ldlr low density lipoprotein receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16127462 10864 Ldlr low density lipoprotein receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21606463 10864 Ldlr low density lipoprotein receptor gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:14739216 10864 Ldlr low density lipoprotein receptor gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:10727439 10864 Ldlr low density lipoprotein receptor gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:18566402 10864 Ldlr low density lipoprotein receptor gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15665085 10864 Ldlr low density lipoprotein receptor gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:21690266 10864 Ldlr low density lipoprotein receptor gene MP:0001863 blood vessel inflammation IAGP N RGD:5509061 20221215 MGI PMID:33356393 10864 Ldlr low density lipoprotein receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12847522 10864 Ldlr low density lipoprotein receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12847522 10864 Ldlr low density lipoprotein receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17872464 10864 Ldlr low density lipoprotein receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20170209 MGI PMID:18160459 10864 Ldlr low density lipoprotein receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15790756 10864 Ldlr low density lipoprotein receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18160655 10864 Ldlr low density lipoprotein receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21606463 10864 Ldlr low density lipoprotein receptor gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10777503 10864 Ldlr low density lipoprotein receptor gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11076954 10864 Ldlr low density lipoprotein receptor gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11893779 10864 Ldlr low density lipoprotein receptor gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14668345 10864 Ldlr low density lipoprotein receptor gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7961705 10864 Ldlr low density lipoprotein receptor gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10727439 10864 Ldlr low density lipoprotein receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12471052 10864 Ldlr low density lipoprotein receptor gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18410513 10864 Ldlr low density lipoprotein receptor gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20221215 MGI PMID:33356393 10864 Ldlr low density lipoprotein receptor gene MP:0002323 decreased susceptibility to hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:11076954 10864 Ldlr low density lipoprotein receptor gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16127462 10864 Ldlr low density lipoprotein receptor gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15665085 10864 Ldlr low density lipoprotein receptor gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:16434491 10864 Ldlr low density lipoprotein receptor gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 10864 Ldlr low density lipoprotein receptor gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14739216 10864 Ldlr low density lipoprotein receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18006500 10864 Ldlr low density lipoprotein receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19318355 10864 Ldlr low density lipoprotein receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22484817 10864 Ldlr low density lipoprotein receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9598833 10864 Ldlr low density lipoprotein receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20150101 MGI PMID:25176150 10864 Ldlr low density lipoprotein receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20240425 MGI PMID:38417553 10864 Ldlr low density lipoprotein receptor gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:16368783 10864 Ldlr low density lipoprotein receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14668345 10864 Ldlr low density lipoprotein receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21606463 10864 Ldlr low density lipoprotein receptor gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0002830 gallstones IEA N RGD:5509061 20111116 MGI 10864 Ldlr low density lipoprotein receptor gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21690266 10864 Ldlr low density lipoprotein receptor gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:15790756 10864 Ldlr low density lipoprotein receptor gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:21690266 10864 Ldlr low density lipoprotein receptor gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:15031124 10864 Ldlr low density lipoprotein receptor gene MP:0003075 abnormal response to CNS ischemic injury IAGP N RGD:5509061 20141003 MGI PMID:19147818 10864 Ldlr low density lipoprotein receptor gene MP:0003099 retina detachment IEA N RGD:5509061 20111116 MGI 10864 Ldlr low density lipoprotein receptor gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:15031124 10864 Ldlr low density lipoprotein receptor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:12639996 10864 Ldlr low density lipoprotein receptor gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21252156 10864 Ldlr low density lipoprotein receptor gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:12969990 10864 Ldlr low density lipoprotein receptor gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:16236385 10864 Ldlr low density lipoprotein receptor gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:18410513 10864 Ldlr low density lipoprotein receptor gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21690266 10864 Ldlr low density lipoprotein receptor gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20240425 MGI PMID:38417553 10864 Ldlr low density lipoprotein receptor gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:19188600 10864 Ldlr low density lipoprotein receptor gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:21690266 10864 Ldlr low density lipoprotein receptor gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19147818 10864 Ldlr low density lipoprotein receptor gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:10727439 10864 Ldlr low density lipoprotein receptor gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:10777503 10864 Ldlr low density lipoprotein receptor gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:19073773 10864 Ldlr low density lipoprotein receptor gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15596719 10864 Ldlr low density lipoprotein receptor gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17615372 10864 Ldlr low density lipoprotein receptor gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12639996 10864 Ldlr low density lipoprotein receptor gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:17885219 10864 Ldlr low density lipoprotein receptor gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18451340 10864 Ldlr low density lipoprotein receptor gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21690266 10864 Ldlr low density lipoprotein receptor gene MP:0003897 abnormal ST segment IAGP N RGD:5509061 20141003 MGI PMID:15031124 10864 Ldlr low density lipoprotein receptor gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0003947 abnormal cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9449704 10864 Ldlr low density lipoprotein receptor gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:11076954 10864 Ldlr low density lipoprotein receptor gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:12969990 10864 Ldlr low density lipoprotein receptor gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:12847522 10864 Ldlr low density lipoprotein receptor gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:8941642 10864 Ldlr low density lipoprotein receptor gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18160655 10864 Ldlr low density lipoprotein receptor gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20150101 MGI PMID:25176150 10864 Ldlr low density lipoprotein receptor gene MP:0003991 arteriosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17885219 10864 Ldlr low density lipoprotein receptor gene MP:0004112 abnormal arteriole morphology IAGP N RGD:5509061 20141003 MGI PMID:16835442 10864 Ldlr low density lipoprotein receptor gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230601 MGI 10864 Ldlr low density lipoprotein receptor gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20150101 MGI PMID:25176150 10864 Ldlr low density lipoprotein receptor gene MP:0004778 increased macrophage derived foam cell number IEA N RGD:5509061 20111116 MGI 10864 Ldlr low density lipoprotein receptor gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:10727439 10864 Ldlr low density lipoprotein receptor gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11375415 10864 Ldlr low density lipoprotein receptor gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12615659 10864 Ldlr low density lipoprotein receptor gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:15031124 10864 Ldlr low density lipoprotein receptor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0005144 abnormal circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16873689 10864 Ldlr low density lipoprotein receptor gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11893779 10864 Ldlr low density lipoprotein receptor gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14668345 10864 Ldlr low density lipoprotein receptor gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17478727 10864 Ldlr low density lipoprotein receptor gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18820241 10864 Ldlr low density lipoprotein receptor gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21606463 10864 Ldlr low density lipoprotein receptor gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8941642 10864 Ldlr low density lipoprotein receptor gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8994037 10864 Ldlr low density lipoprotein receptor gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9449704 10864 Ldlr low density lipoprotein receptor gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9734366 10864 Ldlr low density lipoprotein receptor gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14739216 10864 Ldlr low density lipoprotein receptor gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15591216 10864 Ldlr low density lipoprotein receptor gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16873689 10864 Ldlr low density lipoprotein receptor gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21149301 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10488949 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10712412 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10777503 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11445560 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11893779 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11983917 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12746448 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12969990 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15566430 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15665085 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15840700 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16236385 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16368783 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17885219 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18410513 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18466986 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21149301 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21606463 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21690266 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7538675 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8941642 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9449704 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9598833 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9701246 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20151001 MGI PMID:8656070 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20160218 MGI PMID:24935961 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 10864 Ldlr low density lipoprotein receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10727439 10864 Ldlr low density lipoprotein receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11076954 10864 Ldlr low density lipoprotein receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11375415 10864 Ldlr low density lipoprotein receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12639996 10864 Ldlr low density lipoprotein receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12746502 10864 Ldlr low density lipoprotein receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14739216 10864 Ldlr low density lipoprotein receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15596719 10864 Ldlr low density lipoprotein receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16211093 10864 Ldlr low density lipoprotein receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16873689 10864 Ldlr low density lipoprotein receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19318355 10864 Ldlr low density lipoprotein receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22484817 10864 Ldlr low density lipoprotein receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20220630 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20240425 MGI PMID:38417553 10864 Ldlr low density lipoprotein receptor gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18172117 10864 Ldlr low density lipoprotein receptor gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18385042 10864 Ldlr low density lipoprotein receptor gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:18172117 10864 Ldlr low density lipoprotein receptor gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11893779 10864 Ldlr low density lipoprotein receptor gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14668345 10864 Ldlr low density lipoprotein receptor gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18006500 10864 Ldlr low density lipoprotein receptor gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22484817 10864 Ldlr low density lipoprotein receptor gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20150101 MGI PMID:25176150 10864 Ldlr low density lipoprotein receptor gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16873689 10864 Ldlr low density lipoprotein receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12847522 10864 Ldlr low density lipoprotein receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17872464 10864 Ldlr low density lipoprotein receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21606463 10864 Ldlr low density lipoprotein receptor gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:19073773 10864 Ldlr low density lipoprotein receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12847522 10864 Ldlr low density lipoprotein receptor gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:10712412 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:10727439 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:10764675 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:11445560 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:12615659 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:12690199 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:12746502 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15031124 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15591216 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15665085 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15834123 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:16211093 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:16434491 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:16565511 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:16880330 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17038633 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17615372 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17872464 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:18250194 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:18451340 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:21149301 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:8994037 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:9701246 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20151001 MGI PMID:8656070 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20160218 MGI PMID:24935961 10864 Ldlr low density lipoprotein receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20170209 MGI PMID:18160459 10864 Ldlr low density lipoprotein receptor gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12690199 10864 Ldlr low density lipoprotein receptor gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:14739216 10864 Ldlr low density lipoprotein receptor gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15591216 10864 Ldlr low density lipoprotein receptor gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16127462 10864 Ldlr low density lipoprotein receptor gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17038633 10864 Ldlr low density lipoprotein receptor gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17478727 10864 Ldlr low density lipoprotein receptor gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18466986 10864 Ldlr low density lipoprotein receptor gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19188600 10864 Ldlr low density lipoprotein receptor gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19723498 10864 Ldlr low density lipoprotein receptor gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:21606463 10864 Ldlr low density lipoprotein receptor gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:22484817 10864 Ldlr low density lipoprotein receptor gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20151001 MGI PMID:8656070 10864 Ldlr low density lipoprotein receptor gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20160218 MGI PMID:24935961 10864 Ldlr low density lipoprotein receptor gene MP:0005340 abnormal susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15665085 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11375415 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11520791 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11581143 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11983917 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12639996 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15596719 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16565511 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16624897 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16873689 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17478727 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18006500 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18192239 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9734366 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20150101 MGI PMID:25176150 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20191219 MGI PMID:30944250 10864 Ldlr low density lipoprotein receptor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20201217 MGI PMID:31163988 10864 Ldlr low density lipoprotein receptor gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:11893779 10864 Ldlr low density lipoprotein receptor gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:14739216 10864 Ldlr low density lipoprotein receptor gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:16873689 10864 Ldlr low density lipoprotein receptor gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18385042 10864 Ldlr low density lipoprotein receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12746502 10864 Ldlr low density lipoprotein receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12847522 10864 Ldlr low density lipoprotein receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17872464 10864 Ldlr low density lipoprotein receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:14668345 10864 Ldlr low density lipoprotein receptor gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:16873689 10864 Ldlr low density lipoprotein receptor gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20201015 MGI PMID:28636934 10864 Ldlr low density lipoprotein receptor gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16880330 10864 Ldlr low density lipoprotein receptor gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:19147818 10864 Ldlr low density lipoprotein receptor gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:19147818 10864 Ldlr low density lipoprotein receptor gene MP:0006116 calcified aortic valve IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0006134 artery occlusion IAGP N RGD:5509061 20141003 MGI PMID:12690199 10864 Ldlr low density lipoprotein receptor gene MP:0006238 abnormal choriocapillaris morphology IAGP N RGD:5509061 20141003 MGI PMID:18172117 10864 Ldlr low density lipoprotein receptor gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:12690199 10864 Ldlr low density lipoprotein receptor gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0008243 abnormal macrophage derived foam cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17885219 10864 Ldlr low density lipoprotein receptor gene MP:0008294 abnormal adrenal gland zona fasciculata morphology IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0008431 abnormal short-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:15207278 10864 Ldlr low density lipoprotein receptor gene MP:0008431 abnormal short-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:16835442 10864 Ldlr low density lipoprotein receptor gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:16236385 10864 Ldlr low density lipoprotein receptor gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:18410513 10864 Ldlr low density lipoprotein receptor gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18250194 10864 Ldlr low density lipoprotein receptor gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15665085 10864 Ldlr low density lipoprotein receptor gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18192239 10864 Ldlr low density lipoprotein receptor gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:15665085 10864 Ldlr low density lipoprotein receptor gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:15207278 10864 Ldlr low density lipoprotein receptor gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:17720268 10864 Ldlr low density lipoprotein receptor gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:18172117 10864 Ldlr low density lipoprotein receptor gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:17478727 10864 Ldlr low density lipoprotein receptor gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:17478727 10864 Ldlr low density lipoprotein receptor gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18410513 10864 Ldlr low density lipoprotein receptor gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:18410513 10864 Ldlr low density lipoprotein receptor gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:12746502 10864 Ldlr low density lipoprotein receptor gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20181227 MGI 10864 Ldlr low density lipoprotein receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22484817 10864 Ldlr low density lipoprotein receptor gene MP:0008900 abnormal uterine fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11445560 10864 Ldlr low density lipoprotein receptor gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21690266 10864 Ldlr low density lipoprotein receptor gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20240425 MGI PMID:38417553 10864 Ldlr low density lipoprotein receptor gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:9326295 10864 Ldlr low density lipoprotein receptor gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12746502 10864 Ldlr low density lipoprotein receptor gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:18250194 10864 Ldlr low density lipoprotein receptor gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12690199 10864 Ldlr low density lipoprotein receptor gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:21252156 10864 Ldlr low density lipoprotein receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12847522 10864 Ldlr low density lipoprotein receptor gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20201015 MGI PMID:28636934 10864 Ldlr low density lipoprotein receptor gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20240425 MGI PMID:38417553 10864 Ldlr low density lipoprotein receptor gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11445560 10864 Ldlr low density lipoprotein receptor gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21690266 10864 Ldlr low density lipoprotein receptor gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22484817 10864 Ldlr low density lipoprotein receptor gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20150101 MGI PMID:25176150 10864 Ldlr low density lipoprotein receptor gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:18160655 10864 Ldlr low density lipoprotein receptor gene MP:0010052 increased grip strength IAGP N RGD:5509061 20141003 MGI PMID:18466986 10864 Ldlr low density lipoprotein receptor gene MP:0010072 increased pruritus IAGP N RGD:5509061 20141003 MGI PMID:12937162 10864 Ldlr low density lipoprotein receptor gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 10864 Ldlr low density lipoprotein receptor gene MP:0010139 aortitis IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0010161 decreased brain cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18160655 10864 Ldlr low density lipoprotein receptor gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:18466986 10864 Ldlr low density lipoprotein receptor gene MP:0010332 abnormal circulating apolipoprotein level IAGP N RGD:5509061 20141003 MGI PMID:9449704 10864 Ldlr low density lipoprotein receptor gene MP:0010333 abnormal circulating apolipoprotein E level IAGP N RGD:5509061 20141003 MGI PMID:9449704 10864 Ldlr low density lipoprotein receptor gene MP:0010574 dilated aorta IAGP N RGD:5509061 20141003 MGI PMID:12690199 10864 Ldlr low density lipoprotein receptor gene MP:0010659 abdominal aorta aneurysm IAGP N RGD:5509061 20141003 MGI PMID:12690199 10864 Ldlr low density lipoprotein receptor gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20141003 MGI PMID:12690199 10864 Ldlr low density lipoprotein receptor gene MP:0010997 decreased aorta wall thickness IAGP N RGD:5509061 20141003 MGI PMID:21252156 10864 Ldlr low density lipoprotein receptor gene MP:0011081 decreased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15834123 10864 Ldlr low density lipoprotein receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17155952 10864 Ldlr low density lipoprotein receptor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17615372 10864 Ldlr low density lipoprotein receptor gene MP:0011572 abnormal aorta bulb morphology IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0011579 decreased lipoprotein lipase activity IAGP N RGD:5509061 20141003 MGI PMID:14668345 10864 Ldlr low density lipoprotein receptor gene MP:0011897 decreased circulating unsaturated transferrin level IEA N RGD:5509061 20181227 MGI 10864 Ldlr low density lipoprotein receptor gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:17960025 10864 Ldlr low density lipoprotein receptor gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0012223 increased circulating prothrombin level IAGP N RGD:5509061 20141003 MGI PMID:16434491 10864 Ldlr low density lipoprotein receptor gene MP:0012224 abnormal sterol level IAGP N RGD:5509061 20150101 MGI PMID:25176150 10864 Ldlr low density lipoprotein receptor gene MP:0012326 increased circulating antithrombin level IAGP N RGD:5509061 20141003 MGI PMID:16434491 10864 Ldlr low density lipoprotein receptor gene MP:0012329 increased circulating factor VIII level IAGP N RGD:5509061 20201002 MGI PMID:14739216 10864 Ldlr low density lipoprotein receptor gene MP:0012329 increased circulating factor VIII level IAGP N RGD:5509061 20201002 MGI PMID:15840700 10864 Ldlr low density lipoprotein receptor gene MP:0012355 decreased prothrombin time IAGP N RGD:5509061 20141003 MGI PMID:16434491 10864 Ldlr low density lipoprotein receptor gene MP:0012358 decreased partial thromboplastin time IAGP N RGD:5509061 20201002 MGI PMID:16434491 10864 Ldlr low density lipoprotein receptor gene MP:0012688 abnormal heart ventricles weight IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0013277 abnormal fasting circulating glucose level IAGP N RGD:5509061 20160609 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:11530237 10864 Ldlr low density lipoprotein receptor gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:18410513 10864 Ldlr low density lipoprotein receptor gene MP:0014476 abnormal feces lipid level IAGP N RGD:5509061 20240704 MGI PMID:25176150 10864 Ldlr low density lipoprotein receptor gene MP:0020099 increased susceptibility to diet-induced aortic fatty streak lesions IAGP N RGD:5509061 20200820 MGI PMID:28917158 10864 Ldlr low density lipoprotein receptor gene MP:0020325 abnormal beige fat cell morphology IAGP N RGD:5509061 20201015 MGI PMID:28636934 10864 Ldlr low density lipoprotein receptor gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:11520791 10864 Ldlr low density lipoprotein receptor gene MP:0031076 decreased circulating troponin level IAGP N RGD:5509061 20200618 MGI PMID:15031124 10864 Ldlr low density lipoprotein receptor gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21690266 10864 Ldlr low density lipoprotein receptor gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21690266 10864 Ldlr low density lipoprotein receptor gene MP:0031165 increased circulating von Willebrand factor level IAGP N RGD:5509061 20201015 MGI PMID:14739216 10864 Ldlr low density lipoprotein receptor gene MP:0031165 increased circulating von Willebrand factor level IAGP N RGD:5509061 20201015 MGI PMID:15840700 10864 Ldlr low density lipoprotein receptor gene MP:0031273 decreased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:21252156 10864 Ldlr low density lipoprotein receptor gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:18466986 10864 Ldlr low density lipoprotein receptor gene MP:0031510 increased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:12690199 10864 Ldlr low density lipoprotein receptor gene MP:0031566 small aortic valve IAGP N RGD:5509061 20240125 MGI PMID:25231636 10864 Ldlr low density lipoprotein receptor gene MP:0031632 increased lung cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:18160655 10865 Lepr leptin receptor gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20170330 MGI PMID:26441241 10865 Lepr leptin receptor gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:3882910 10865 Lepr leptin receptor gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200402 MGI 10865 Lepr leptin receptor gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22414803 10865 Lepr leptin receptor gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177042 10865 Lepr leptin receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177042 10865 Lepr leptin receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12136396 10865 Lepr leptin receptor gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16123339 10865 Lepr leptin receptor gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21745644 10865 Lepr leptin receptor gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:9299565 10865 Lepr leptin receptor gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:6993269 10865 Lepr leptin receptor gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20200402 MGI 10865 Lepr leptin receptor gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16373670 10865 Lepr leptin receptor gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 10865 Lepr leptin receptor gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16373670 10865 Lepr leptin receptor gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22281595 10865 Lepr leptin receptor gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:431046 10865 Lepr leptin receptor gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20210415 MGI PMID:32233916 10865 Lepr leptin receptor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12885755 10865 Lepr leptin receptor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:431046 10865 Lepr leptin receptor gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22281595 10865 Lepr leptin receptor gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:16113078 10865 Lepr leptin receptor gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17023554 10865 Lepr leptin receptor gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:3882910 10865 Lepr leptin receptor gene MP:0000592 short tail IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:10708583 10865 Lepr leptin receptor gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:3882910 10865 Lepr leptin receptor gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:22414803 10865 Lepr leptin receptor gene MP:0000642 enlarged adrenal glands IEA N RGD:5509061 20111116 MGI 10865 Lepr leptin receptor gene MP:0000643 absent adrenal medulla IEA N RGD:5509061 20111116 MGI 10865 Lepr leptin receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22281595 10865 Lepr leptin receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:3882910 10865 Lepr leptin receptor gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22281595 10865 Lepr leptin receptor gene MP:0000745 tremors IEA N RGD:5509061 20170105 MGI 10865 Lepr leptin receptor gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:6991317 10865 Lepr leptin receptor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:12502493 10865 Lepr leptin receptor gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:23119079 10865 Lepr leptin receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:23119079 10865 Lepr leptin receptor gene MP:0001143 constricted vagina orifice IAGP N RGD:5509061 20141003 MGI PMID:378276 10865 Lepr leptin receptor gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20200402 MGI 10865 Lepr leptin receptor gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:15070774 10865 Lepr leptin receptor gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11602618 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12502493 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15885672 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16423694 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16919419 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16971655 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20852026 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:21084451 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:21745644 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:21907138 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22326220 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22522563 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23986522 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:5918576 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:6993269 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:9845674 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20150514 MGI PMID:25176149 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20151126 MGI PMID:25353183 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20151203 MGI PMID:24024119 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20190905 MGI PMID:22118645 10865 Lepr leptin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:10666131 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:10708583 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:11602618 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12136396 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12730408 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12885755 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15070774 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15207242 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15389315 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15685168 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:16113078 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:16123339 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:16423694 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:16443782 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:16735799 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:21084451 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:21346177 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:3882910 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:6991317 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:6993269 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:8177042 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:9845674 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20150416 MGI PMID:25157166 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20150514 MGI PMID:25176149 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20170330 MGI PMID:26441241 10865 Lepr leptin receptor gene MP:0001261 obese IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17415414 10865 Lepr leptin receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22510882 10865 Lepr leptin receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170713 MGI PMID:27402271 10865 Lepr leptin receptor gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15309293 10865 Lepr leptin receptor gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16123339 10865 Lepr leptin receptor gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:6993269 10865 Lepr leptin receptor gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:22326220 10865 Lepr leptin receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16735799 10865 Lepr leptin receptor gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16998795 10865 Lepr leptin receptor gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:16043866 10865 Lepr leptin receptor gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20230601 MGI 10865 Lepr leptin receptor gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:378276 10865 Lepr leptin receptor gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20220519 MGI PMID:35349646 10865 Lepr leptin receptor gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 10865 Lepr leptin receptor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21907138 10865 Lepr leptin receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22522563 10865 Lepr leptin receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0001405 impaired coordination IEA N RGD:5509061 20190110 MGI 10865 Lepr leptin receptor gene MP:0001406 abnormal gait IEA N RGD:5509061 20170105 MGI 10865 Lepr leptin receptor gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 10865 Lepr leptin receptor gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:10666131 10865 Lepr leptin receptor gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:10708583 10865 Lepr leptin receptor gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:5918576 10865 Lepr leptin receptor gene MP:0001426 polydipsia IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:10666131 10865 Lepr leptin receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:15389315 10865 Lepr leptin receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:15685168 10865 Lepr leptin receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:16123339 10865 Lepr leptin receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:21745644 10865 Lepr leptin receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:3882910 10865 Lepr leptin receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:5918576 10865 Lepr leptin receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:6993269 10865 Lepr leptin receptor gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12150780 10865 Lepr leptin receptor gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12150780 10865 Lepr leptin receptor gene MP:0001512 trunk curl IEA N RGD:5509061 20181227 MGI 10865 Lepr leptin receptor gene MP:0001513 limb grasping IEA N RGD:5509061 20181227 MGI 10865 Lepr leptin receptor gene MP:0001523 impaired righting response IEA N RGD:5509061 20181227 MGI 10865 Lepr leptin receptor gene MP:0001525 impaired balance IEA N RGD:5509061 20190110 MGI 10865 Lepr leptin receptor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12540618 10865 Lepr leptin receptor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16443782 10865 Lepr leptin receptor gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:21346177 10865 Lepr leptin receptor gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:15685168 10865 Lepr leptin receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:8177042 10865 Lepr leptin receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170330 MGI PMID:26441241 10865 Lepr leptin receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16443782 10865 Lepr leptin receptor gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20170330 MGI PMID:26441241 10865 Lepr leptin receptor gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23986522 10865 Lepr leptin receptor gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177042 10865 Lepr leptin receptor gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:10708583 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:11602618 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12136396 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12730408 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15389315 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15685168 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15885672 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16113078 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16123339 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16443782 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16735799 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16971655 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17268472 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19955657 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:22326220 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:22609345 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:23119079 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:23986522 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:24332968 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:3882910 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:6993269 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:8177042 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20150416 MGI PMID:25157166 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20170330 MGI PMID:26441241 10865 Lepr leptin receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11416008 10865 Lepr leptin receptor gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12136396 10865 Lepr leptin receptor gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 10865 Lepr leptin receptor gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:760211 10865 Lepr leptin receptor gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17023554 10865 Lepr leptin receptor gene MP:0001727 abnormal embryo implantation IAGP N RGD:5509061 20220519 MGI PMID:35349646 10865 Lepr leptin receptor gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15070774 10865 Lepr leptin receptor gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:22522563 10865 Lepr leptin receptor gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:10666131 10865 Lepr leptin receptor gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:10708583 10865 Lepr leptin receptor gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:23986522 10865 Lepr leptin receptor gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:10708583 10865 Lepr leptin receptor gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:23986522 10865 Lepr leptin receptor gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:5918576 10865 Lepr leptin receptor gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20150514 MGI PMID:25176149 10865 Lepr leptin receptor gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:17023554 10865 Lepr leptin receptor gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:23119079 10865 Lepr leptin receptor gene MP:0001860 liver inflammation IAGP N RGD:5509061 20190905 MGI PMID:22118645 10865 Lepr leptin receptor gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:16373670 10865 Lepr leptin receptor gene MP:0001868 ovary inflammation IAGP N RGD:5509061 20141003 MGI PMID:23119079 10865 Lepr leptin receptor gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:16123339 10865 Lepr leptin receptor gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:12150780 10865 Lepr leptin receptor gene MP:0001922 reduced male fertility IEA N RGD:5509061 20160721 MGI 10865 Lepr leptin receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:22522563 10865 Lepr leptin receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220519 MGI PMID:35349646 10865 Lepr leptin receptor gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:15389315 10865 Lepr leptin receptor gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:6993269 10865 Lepr leptin receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10666131 10865 Lepr leptin receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:3882910 10865 Lepr leptin receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10666131 10865 Lepr leptin receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:378276 10865 Lepr leptin receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:3882910 10865 Lepr leptin receptor gene MP:0001927 abnormal estrous cycle IEA N RGD:5509061 20120119 MGI 10865 Lepr leptin receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220519 MGI PMID:35349646 10865 Lepr leptin receptor gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:12150780 10865 Lepr leptin receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11416008 10865 Lepr leptin receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12136396 10865 Lepr leptin receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12502493 10865 Lepr leptin receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12540618 10865 Lepr leptin receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15389315 10865 Lepr leptin receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10666131 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10708583 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11602618 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12136396 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12502493 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12730408 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15070774 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15389315 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15685168 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15885672 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16113078 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16123339 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19955657 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20086094 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21745644 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22055502 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22414803 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22522563 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:3882910 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:5918576 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:6993269 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9845674 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20150416 MGI PMID:25157166 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20150514 MGI PMID:25176149 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20170330 MGI PMID:26441241 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10666131 10865 Lepr leptin receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16123339 10865 Lepr leptin receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16735799 10865 Lepr leptin receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:6993269 10865 Lepr leptin receptor gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:10660043 10865 Lepr leptin receptor gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:12540618 10865 Lepr leptin receptor gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16735799 10865 Lepr leptin receptor gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:23986522 10865 Lepr leptin receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11602618 10865 Lepr leptin receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15207242 10865 Lepr leptin receptor gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12150780 10865 Lepr leptin receptor gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16423694 10865 Lepr leptin receptor gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21745644 10865 Lepr leptin receptor gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21907138 10865 Lepr leptin receptor gene MP:0002306 abnormal functional residual capacity IAGP N RGD:5509061 20141003 MGI PMID:16373670 10865 Lepr leptin receptor gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20141003 MGI PMID:16373670 10865 Lepr leptin receptor gene MP:0002333 abnormal lung compliance IAGP N RGD:5509061 20141003 MGI PMID:16373670 10865 Lepr leptin receptor gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:23434755 10865 Lepr leptin receptor gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16380490 10865 Lepr leptin receptor gene MP:0002497 increased IgE level IEA N RGD:5509061 20161201 MGI 10865 Lepr leptin receptor gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:17023554 10865 Lepr leptin receptor gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20190905 MGI PMID:22118645 10865 Lepr leptin receptor gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20200402 MGI 10865 Lepr leptin receptor gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20181227 MGI 10865 Lepr leptin receptor gene MP:0002608 increased hematocrit IEA N RGD:5509061 20170105 MGI 10865 Lepr leptin receptor gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12885755 10865 Lepr leptin receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:11602618 10865 Lepr leptin receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:21346177 10865 Lepr leptin receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20170330 MGI PMID:26441241 10865 Lepr leptin receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20190905 MGI PMID:22118645 10865 Lepr leptin receptor gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:378276 10865 Lepr leptin receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15309293 10865 Lepr leptin receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0002680 decreased corpora lutea number IEA N RGD:5509061 20111116 MGI 10865 Lepr leptin receptor gene MP:0002682 decreased mature ovarian follicle number IEA N RGD:5509061 20111116 MGI 10865 Lepr leptin receptor gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:19955657 10865 Lepr leptin receptor gene MP:0002710 increased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:393618 10865 Lepr leptin receptor gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:6993269 10865 Lepr leptin receptor gene MP:0002716 small male preputial gland IAGP N RGD:5509061 20141003 MGI PMID:378276 10865 Lepr leptin receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15309293 10865 Lepr leptin receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17268472 10865 Lepr leptin receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17415414 10865 Lepr leptin receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9299565 10865 Lepr leptin receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20151126 MGI PMID:25353183 10865 Lepr leptin receptor gene MP:0002764 short tibia IEA N RGD:5509061 20190110 MGI 10865 Lepr leptin receptor gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20170330 MGI PMID:26441241 10865 Lepr leptin receptor gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16043866 10865 Lepr leptin receptor gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:12932425 10865 Lepr leptin receptor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:23986522 10865 Lepr leptin receptor gene MP:0002834 decreased heart weight IEA N RGD:5509061 20201022 MGI 10865 Lepr leptin receptor gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17095713 10865 Lepr leptin receptor gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:16735799 10865 Lepr leptin receptor gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:16971655 10865 Lepr leptin receptor gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:22326220 10865 Lepr leptin receptor gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:23986522 10865 Lepr leptin receptor gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12136396 10865 Lepr leptin receptor gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:22510882 10865 Lepr leptin receptor gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20170713 MGI PMID:27402271 10865 Lepr leptin receptor gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20220519 MGI PMID:35349646 10865 Lepr leptin receptor gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:22609345 10865 Lepr leptin receptor gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20200402 MGI 10865 Lepr leptin receptor gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21745644 10865 Lepr leptin receptor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:5009970 10865 Lepr leptin receptor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20210304 MGI PMID:33186558 10865 Lepr leptin receptor gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20200402 MGI 10865 Lepr leptin receptor gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200402 MGI 10865 Lepr leptin receptor gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20191128 MGI PMID:29551634 10865 Lepr leptin receptor gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23986522 10865 Lepr leptin receptor gene MP:0002981 increased liver weight IAGP N RGD:5509061 20170330 MGI PMID:26441241 10865 Lepr leptin receptor gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 10865 Lepr leptin receptor gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:15885672 10865 Lepr leptin receptor gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19103808 10865 Lepr leptin receptor gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20852026 10865 Lepr leptin receptor gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19103808 10865 Lepr leptin receptor gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:22326220 10865 Lepr leptin receptor gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:3882910 10865 Lepr leptin receptor gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20170105 MGI 10865 Lepr leptin receptor gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:20086094 10865 Lepr leptin receptor gene MP:0003213 decreased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:11101849 10865 Lepr leptin receptor gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:20086094 10865 Lepr leptin receptor gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:21907138 10865 Lepr leptin receptor gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20190905 MGI PMID:22118645 10865 Lepr leptin receptor gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:23119079 10865 Lepr leptin receptor gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:12540618 10865 Lepr leptin receptor gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:16443782 10865 Lepr leptin receptor gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:17360690 10865 Lepr leptin receptor gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24332968 10865 Lepr leptin receptor gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20151203 MGI PMID:24024119 10865 Lepr leptin receptor gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:6991317 10865 Lepr leptin receptor gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:20086094 10865 Lepr leptin receptor gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20150514 MGI PMID:25176149 10865 Lepr leptin receptor gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:12136396 10865 Lepr leptin receptor gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:15685168 10865 Lepr leptin receptor gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:6993269 10865 Lepr leptin receptor gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:16522636 10865 Lepr leptin receptor gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22326220 10865 Lepr leptin receptor gene MP:0003718 maternal effect IAGP N RGD:5509061 20151126 MGI PMID:25353183 10865 Lepr leptin receptor gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201022 MGI 10865 Lepr leptin receptor gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20191128 MGI PMID:29551634 10865 Lepr leptin receptor gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:16443782 10865 Lepr leptin receptor gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:6991317 10865 Lepr leptin receptor gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:16971655 10865 Lepr leptin receptor gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20190905 MGI PMID:22118645 10865 Lepr leptin receptor gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:22326220 10865 Lepr leptin receptor gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:23986522 10865 Lepr leptin receptor gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20170330 MGI PMID:26441241 10865 Lepr leptin receptor gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:8177042 10865 Lepr leptin receptor gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:11416008 10865 Lepr leptin receptor gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:378276 10865 Lepr leptin receptor gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:21084451 10865 Lepr leptin receptor gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:21907138 10865 Lepr leptin receptor gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23119079 10865 Lepr leptin receptor gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23986522 10865 Lepr leptin receptor gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20190905 MGI PMID:22118645 10865 Lepr leptin receptor gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0004120 cardiac ischemia IAGP N RGD:5509061 20141003 MGI PMID:12540618 10865 Lepr leptin receptor gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:19103808 10865 Lepr leptin receptor gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:5009970 10865 Lepr leptin receptor gene MP:0004195 abnormal kidney calyx morphology IAGP N RGD:5509061 20141003 MGI PMID:5009970 10865 Lepr leptin receptor gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:3882910 10865 Lepr leptin receptor gene MP:0004260 enlarged placenta IAGP N RGD:5509061 20151126 MGI PMID:25353183 10865 Lepr leptin receptor gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20190110 MGI 10865 Lepr leptin receptor gene MP:0004514 dystocia IAGP N RGD:5509061 20220519 MGI PMID:35349646 10865 Lepr leptin receptor gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:6339122 10865 Lepr leptin receptor gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21907138 10865 Lepr leptin receptor gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21346177 10865 Lepr leptin receptor gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:17095713 10865 Lepr leptin receptor gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20150514 MGI PMID:25176149 10865 Lepr leptin receptor gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:12502493 10865 Lepr leptin receptor gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:12502493 10865 Lepr leptin receptor gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:16549076 10865 Lepr leptin receptor gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20201022 MGI 10865 Lepr leptin receptor gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16380490 10865 Lepr leptin receptor gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 10865 Lepr leptin receptor gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 10865 Lepr leptin receptor gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:21393862 10865 Lepr leptin receptor gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:21084451 10865 Lepr leptin receptor gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:378276 10865 Lepr leptin receptor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16443782 10865 Lepr leptin receptor gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177042 10865 Lepr leptin receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:3882910 10865 Lepr leptin receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177042 10865 Lepr leptin receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20170330 MGI PMID:26441241 10865 Lepr leptin receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:15685168 10865 Lepr leptin receptor gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:16123339 10865 Lepr leptin receptor gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:20852026 10865 Lepr leptin receptor gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12730408 10865 Lepr leptin receptor gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15685168 10865 Lepr leptin receptor gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:6993269 10865 Lepr leptin receptor gene MP:0005257 abnormal intraocular pressure IAGP N RGD:5509061 20141003 MGI PMID:11532192 10865 Lepr leptin receptor gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16971655 10865 Lepr leptin receptor gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:20375117 10865 Lepr leptin receptor gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:23986522 10865 Lepr leptin receptor gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:20086094 10865 Lepr leptin receptor gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:11101849 10865 Lepr leptin receptor gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22510882 10865 Lepr leptin receptor gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20151203 MGI PMID:24024119 10865 Lepr leptin receptor gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21907138 10865 Lepr leptin receptor gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22522563 10865 Lepr leptin receptor gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20150514 MGI PMID:25176149 10865 Lepr leptin receptor gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22510882 10865 Lepr leptin receptor gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:9299565 10865 Lepr leptin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11416008 10865 Lepr leptin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12136396 10865 Lepr leptin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15070774 10865 Lepr leptin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22055502 10865 Lepr leptin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22414803 10865 Lepr leptin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20151126 MGI PMID:25353183 10865 Lepr leptin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12136396 10865 Lepr leptin receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16735799 10865 Lepr leptin receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16971655 10865 Lepr leptin receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:5009970 10865 Lepr leptin receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20210304 MGI PMID:33186558 10865 Lepr leptin receptor gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12540618 10865 Lepr leptin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:10666131 10865 Lepr leptin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12136396 10865 Lepr leptin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17268472 10865 Lepr leptin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:20852026 10865 Lepr leptin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21346177 10865 Lepr leptin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22414803 10865 Lepr leptin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20151203 MGI PMID:24024119 10865 Lepr leptin receptor gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12540618 10865 Lepr leptin receptor gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16443782 10865 Lepr leptin receptor gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15207242 10865 Lepr leptin receptor gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16423694 10865 Lepr leptin receptor gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16919419 10865 Lepr leptin receptor gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17415414 10865 Lepr leptin receptor gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16423694 10865 Lepr leptin receptor gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:23119079 10865 Lepr leptin receptor gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20200402 MGI 10865 Lepr leptin receptor gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:6991317 10865 Lepr leptin receptor gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:6991317 10865 Lepr leptin receptor gene MP:0005431 decreased oocyte number IEA N RGD:5509061 20111222 MGI 10865 Lepr leptin receptor gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:20086094 10865 Lepr leptin receptor gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:9299565 10865 Lepr leptin receptor gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:16423694 10865 Lepr leptin receptor gene MP:0005451 abnormal body composition IAGP N RGD:5509061 20141003 MGI PMID:11602618 10865 Lepr leptin receptor gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:11416008 10865 Lepr leptin receptor gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:15389315 10865 Lepr leptin receptor gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:16123339 10865 Lepr leptin receptor gene MP:0005457 abnormal percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:21907138 10865 Lepr leptin receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:16123339 10865 Lepr leptin receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:20086094 10865 Lepr leptin receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:23119079 10865 Lepr leptin receptor gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:22522563 10865 Lepr leptin receptor gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12136396 10865 Lepr leptin receptor gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:6993269 10865 Lepr leptin receptor gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:16971655 10865 Lepr leptin receptor gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:15685168 10865 Lepr leptin receptor gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0005535 abnormal body temperature IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0005540 decreased urine albumin level IAGP N RGD:5509061 20141003 MGI PMID:12651605 10865 Lepr leptin receptor gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16043866 10865 Lepr leptin receptor gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16971655 10865 Lepr leptin receptor gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:23986522 10865 Lepr leptin receptor gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0005557 increased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:12651605 10865 Lepr leptin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10666131 10865 Lepr leptin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11416008 10865 Lepr leptin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12502493 10865 Lepr leptin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15070774 10865 Lepr leptin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15389315 10865 Lepr leptin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16919419 10865 Lepr leptin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20086094 10865 Lepr leptin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22414803 10865 Lepr leptin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22522563 10865 Lepr leptin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:5918576 10865 Lepr leptin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:6991317 10865 Lepr leptin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:9845674 10865 Lepr leptin receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15309293 10865 Lepr leptin receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15389315 10865 Lepr leptin receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17268472 10865 Lepr leptin receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17360690 10865 Lepr leptin receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:9299565 10865 Lepr leptin receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20170713 MGI PMID:27402271 10865 Lepr leptin receptor gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 10865 Lepr leptin receptor gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20170105 MGI 10865 Lepr leptin receptor gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16735799 10865 Lepr leptin receptor gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20200402 MGI 10865 Lepr leptin receptor gene MP:0005576 decreased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:16373670 10865 Lepr leptin receptor gene MP:0005580 periinsulitis IAGP N RGD:5509061 20141003 MGI PMID:16123339 10865 Lepr leptin receptor gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16735799 10865 Lepr leptin receptor gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20210415 MGI PMID:32233916 10865 Lepr leptin receptor gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 10865 Lepr leptin receptor gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20141003 MGI PMID:378276 10865 Lepr leptin receptor gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:16423694 10865 Lepr leptin receptor gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:20086094 10865 Lepr leptin receptor gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20190905 MGI PMID:22118645 10865 Lepr leptin receptor gene MP:0005661 decreased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:19103808 10865 Lepr leptin receptor gene MP:0005664 decreased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:19103808 10865 Lepr leptin receptor gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20170713 MGI PMID:27402271 10865 Lepr leptin receptor gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17415414 10865 Lepr leptin receptor gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:20086094 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:10666131 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11602618 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15070774 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15207242 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15389315 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16123339 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16373670 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16423694 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:20086094 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21084451 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21907138 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22522563 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23119079 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:9845674 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20150514 MGI PMID:25176149 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20151126 MGI PMID:25353183 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20151203 MGI PMID:24024119 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20170330 MGI PMID:26441241 10865 Lepr leptin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:22326220 10865 Lepr leptin receptor gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23119079 10865 Lepr leptin receptor gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16971655 10865 Lepr leptin receptor gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12540618 10865 Lepr leptin receptor gene MP:0006315 abnormal urine protein level IAGP N RGD:5509061 20141003 MGI PMID:23986513 10865 Lepr leptin receptor gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15207242 10865 Lepr leptin receptor gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16691291 10865 Lepr leptin receptor gene MP:0006353 increased glycosylated hemoglobin level IAGP N RGD:5509061 20141003 MGI PMID:16113078 10865 Lepr leptin receptor gene MP:0006353 increased glycosylated hemoglobin level IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16373670 10865 Lepr leptin receptor gene MP:0008295 abnormal adrenal gland zona reticularis morphology IEA N RGD:5509061 20111116 MGI 10865 Lepr leptin receptor gene MP:0008329 decreased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:21084451 10865 Lepr leptin receptor gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:10660043 10865 Lepr leptin receptor gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:12150780 10865 Lepr leptin receptor gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:16373670 10865 Lepr leptin receptor gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17023554 10865 Lepr leptin receptor gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:16373670 10865 Lepr leptin receptor gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17023554 10865 Lepr leptin receptor gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17023554 10865 Lepr leptin receptor gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:16373670 10865 Lepr leptin receptor gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 10865 Lepr leptin receptor gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 10865 Lepr leptin receptor gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:21346177 10865 Lepr leptin receptor gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20170119 MGI PMID:22510882 10865 Lepr leptin receptor gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21393862 10865 Lepr leptin receptor gene MP:0008902 abnormal renal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15207242 10865 Lepr leptin receptor gene MP:0008902 abnormal renal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16423694 10865 Lepr leptin receptor gene MP:0008903 abnormal mesenteric fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15207242 10865 Lepr leptin receptor gene MP:0008903 abnormal mesenteric fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16423694 10865 Lepr leptin receptor gene MP:0008962 abnormal carbon dioxide production IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0009008 delayed estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0009008 delayed estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:22522563 10865 Lepr leptin receptor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:378276 10865 Lepr leptin receptor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20161027 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0009010 abnormal diestrus IAGP N RGD:5509061 20141003 MGI PMID:378276 10865 Lepr leptin receptor gene MP:0009019 abnormal metestrus IAGP N RGD:5509061 20141003 MGI PMID:378276 10865 Lepr leptin receptor gene MP:0009021 absent estrus IAGP N RGD:5509061 20141003 MGI PMID:12594516 10865 Lepr leptin receptor gene MP:0009021 absent estrus IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:19955657 10865 Lepr leptin receptor gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:22414803 10865 Lepr leptin receptor gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22510882 10865 Lepr leptin receptor gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:6993269 10865 Lepr leptin receptor gene MP:0009255 degranulated pancreatic beta cells IAGP N RGD:5509061 20141003 MGI PMID:16123339 10865 Lepr leptin receptor gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17415414 10865 Lepr leptin receptor gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21907138 10865 Lepr leptin receptor gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20150514 MGI PMID:25176149 10865 Lepr leptin receptor gene MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:20068132 10865 Lepr leptin receptor gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20150416 MGI PMID:25157166 10865 Lepr leptin receptor gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20170330 MGI PMID:26441241 10865 Lepr leptin receptor gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23864684 10865 Lepr leptin receptor gene MP:0009488 abnormal pancreatic islet cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19955657 10865 Lepr leptin receptor gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20170330 MGI PMID:26441241 10865 Lepr leptin receptor gene MP:0009673 increased birth weight IAGP N RGD:5509061 20151126 MGI PMID:25353183 10865 Lepr leptin receptor gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16113078 10865 Lepr leptin receptor gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:22609345 10865 Lepr leptin receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11416008 10865 Lepr leptin receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11602618 10865 Lepr leptin receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15070774 10865 Lepr leptin receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15207242 10865 Lepr leptin receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16423694 10865 Lepr leptin receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21084451 10865 Lepr leptin receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21745644 10865 Lepr leptin receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21907138 10865 Lepr leptin receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22522563 10865 Lepr leptin receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:3882910 10865 Lepr leptin receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20151203 MGI PMID:24024119 10865 Lepr leptin receptor gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0010045 increased omental fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 10865 Lepr leptin receptor gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20200402 MGI 10865 Lepr leptin receptor gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200402 MGI 10865 Lepr leptin receptor gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20141003 MGI PMID:21907138 10865 Lepr leptin receptor gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22326958 10865 Lepr leptin receptor gene MP:0010400 increased liver glycogen level IEA N RGD:5509061 20150611 MGI 10865 Lepr leptin receptor gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21084451 10865 Lepr leptin receptor gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190110 MGI 10865 Lepr leptin receptor gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190110 MGI 10865 Lepr leptin receptor gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:10660043 10865 Lepr leptin receptor gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20150514 MGI PMID:25176149 10865 Lepr leptin receptor gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:16443782 10865 Lepr leptin receptor gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:12540618 10865 Lepr leptin receptor gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:16443782 10865 Lepr leptin receptor gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20150514 MGI PMID:25176149 10865 Lepr leptin receptor gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19582570 10865 Lepr leptin receptor gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:15070774 10865 Lepr leptin receptor gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:15389315 10865 Lepr leptin receptor gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:19015522 10865 Lepr leptin receptor gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20141003 MGI PMID:22281595 10865 Lepr leptin receptor gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0011312 abnormal kidney afferent arteriole morphology IAGP N RGD:5509061 20141003 MGI PMID:16971655 10865 Lepr leptin receptor gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:16971655 10865 Lepr leptin receptor gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:22326220 10865 Lepr leptin receptor gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20210304 MGI PMID:33186558 10865 Lepr leptin receptor gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20240502 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0011369 increased renal glomerulus apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22326220 10865 Lepr leptin receptor gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16971655 10865 Lepr leptin receptor gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:16971655 10865 Lepr leptin receptor gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:22326220 10865 Lepr leptin receptor gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:16971655 10865 Lepr leptin receptor gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20240509 MGI PMID:36863097 10865 Lepr leptin receptor gene MP:0011561 renal glomerulus lipidosis IAGP N RGD:5509061 20210304 MGI PMID:33186558 10865 Lepr leptin receptor gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:11416008 10865 Lepr leptin receptor gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:16423694 10865 Lepr leptin receptor gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:22522563 10865 Lepr leptin receptor gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:23986522 10865 Lepr leptin receptor gene MP:0011939 increased food intake IAGP N RGD:5509061 20151203 MGI PMID:24024119 10865 Lepr leptin receptor gene MP:0011939 increased food intake IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:23986522 10865 Lepr leptin receptor gene MP:0012008 delayed parturition IAGP N RGD:5509061 20220519 MGI PMID:35349646 10865 Lepr leptin receptor gene MP:0012555 decreased cell death IEA N RGD:5509061 20161201 MGI 10865 Lepr leptin receptor gene MP:0013246 abnormal peptide metabolism IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20190110 MGI 10865 Lepr leptin receptor gene MP:0014121 increased pancreatic islet cell apoptosis IAGP N RGD:5509061 20160324 MGI PMID:19955657 10865 Lepr leptin receptor gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20170713 MGI PMID:27402271 10865 Lepr leptin receptor gene MP:0014441 decreased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:11416008 10865 Lepr leptin receptor gene MP:0014441 decreased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:21907138 10865 Lepr leptin receptor gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20161201 MGI 10865 Lepr leptin receptor gene MP:0020087 increased susceptibility to non-insulin-dependent diabetes IAGP N RGD:5509061 20150416 MGI PMID:25157166 10865 Lepr leptin receptor gene MP:0020089 increased susceptibility to diet-induced non-insulin dependent diabetes IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20170202 MGI PMID:23119079 10865 Lepr leptin receptor gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20171012 MGI PMID:15309293 10865 Lepr leptin receptor gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:823065 10865 Lepr leptin receptor gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:823065 10865 Lepr leptin receptor gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:16373670 10865 Lepr leptin receptor gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:22118645 10865 Lepr leptin receptor gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:22118645 10865 Lepr leptin receptor gene MP:0031269 increased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20231116 MGI PMID:34390703 10865 Lepr leptin receptor gene MP:0031419 delayed estrus IAGP N RGD:5509061 20220630 MGI PMID:24024119 10865 Lepr leptin receptor gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240321 MGI PMID:21346177 10865 Lepr leptin receptor gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240321 MGI PMID:23119079 10868 Lgals9 lectin, galactose binding, soluble 9 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 10868 Lgals9 lectin, galactose binding, soluble 9 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20150226 MGI PMID:23118208 10868 Lgals9 lectin, galactose binding, soluble 9 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20150226 MGI PMID:23118208 10868 Lgals9 lectin, galactose binding, soluble 9 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20150226 MGI PMID:23118208 10868 Lgals9 lectin, galactose binding, soluble 9 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:18282810 10868 Lgals9 lectin, galactose binding, soluble 9 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18282810 10868 Lgals9 lectin, galactose binding, soluble 9 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 10868 Lgals9 lectin, galactose binding, soluble 9 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20150226 MGI PMID:23118208 10868 Lgals9 lectin, galactose binding, soluble 9 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:18282810 10868 Lgals9 lectin, galactose binding, soluble 9 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20150226 MGI PMID:23118208 10868 Lgals9 lectin, galactose binding, soluble 9 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20150226 MGI PMID:23118208 10868 Lgals9 lectin, galactose binding, soluble 9 gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20150226 MGI PMID:23118208 10868 Lgals9 lectin, galactose binding, soluble 9 gene MP:0020155 enhanced humoral immune response IAGP N RGD:5509061 20150226 MGI PMID:23118208 10869 Lhb luteinizing hormone beta gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:17350160 10869 Lhb luteinizing hormone beta gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17350160 10869 Lhb luteinizing hormone beta gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17350160 10869 Lhb luteinizing hormone beta gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17350160 10869 Lhb luteinizing hormone beta gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17350160 10869 Lhb luteinizing hormone beta gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0002774 small prostate gland IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0002779 abnormal sex gland secretion IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0003527 small vulva IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:17350160 10869 Lhb luteinizing hormone beta gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:17350160 10869 Lhb luteinizing hormone beta gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17350160 10869 Lhb luteinizing hormone beta gene MP:0008258 thin endometrium IAGP N RGD:5509061 20141003 MGI PMID:17350160 10869 Lhb luteinizing hormone beta gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17350160 10869 Lhb luteinizing hormone beta gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:17350160 10869 Lhb luteinizing hormone beta gene MP:0009202 small external male genitalia IAGP N RGD:5509061 20141003 MGI PMID:15569941 10869 Lhb luteinizing hormone beta gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20220407 MGI PMID:17350160 10869 Lhb luteinizing hormone beta gene MP:0013602 abnormal Leydig cell differentiation IAGP N RGD:5509061 20150319 MGI PMID:17350160 10869 Lhb luteinizing hormone beta gene MP:0013737 small bulbourethral gland IAGP N RGD:5509061 20150416 MGI PMID:15569941 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20181227 MGI 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0000601 small liver IEA N RGD:5509061 20160811 MGI 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0000664 small prostate gland anterior lobe IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0000671 bulbourethral gland hypoplasia IAGP N RGD:5509061 20150416 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0000692 small spleen IEA N RGD:5509061 20160811 MGI 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0000706 small thymus IEA N RGD:5509061 20160811 MGI 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0000774 decreased brain size IEA N RGD:5509061 20160811 MGI 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001142 abnormal vagina orifice morphology IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:23861372 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001378 abnormal ejaculation IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002188 small heart IEA N RGD:5509061 20160811 MGI 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002254 reproductive system inflammation IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:12604639 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:12604639 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:12604639 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002691 small stomach IEA N RGD:5509061 20160811 MGI 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:23861372 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002774 small prostate gland IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:23861372 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002785 absent Leydig cells IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:23861372 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0002997 enlarged seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:23861372 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0003378 early sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:23861372 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0003531 abnormal vagina development IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0003596 epididymis inflammation IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0003608 prostate gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0003611 scrotum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0003611 scrotum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0003641 small lung IEA N RGD:5509061 20160811 MGI 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23861372 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004909 increased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:23861372 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004928 increased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:23861372 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004932 epididymis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004932 epididymis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12604639 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004958 enlarged prostate gland IAGP N RGD:5509061 20141003 MGI PMID:23861372 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0004961 increased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:23861372 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005147 prostate gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005147 prostate gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005148 seminal vesicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005148 seminal vesicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005188 small penis IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005188 small penis IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005188 small penis IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0008257 thin myometrium IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0008258 thin endometrium IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0009021 absent estrus IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0009081 thin uterus IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0009081 thin uterus IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0009088 thin uterine horn IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0009096 decreased endometrial gland number IAGP N RGD:5509061 20141003 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0009097 absent endometrial glands IAGP N RGD:5509061 20141003 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0009201 external male genitalia atrophy IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0009214 vas deferens hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20141003 MGI PMID:23861372 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0011533 increased urine major urinary protein level IAGP N RGD:5509061 20141003 MGI PMID:23861372 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0013307 increased adrenal gland weight IAGP N RGD:5509061 20150416 MGI PMID:15514086 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0013604 abnormal adult Leydig cell differentiation IAGP N RGD:5509061 20150319 MGI PMID:11145749 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0013604 abnormal adult Leydig cell differentiation IAGP N RGD:5509061 20150319 MGI PMID:23861372 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220421 MGI PMID:12604639 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0014193 decreased epididymal cell proliferation IAGP N RGD:5509061 20160526 MGI PMID:12604639 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0014269 decreased testes secretion IAGP N RGD:5509061 20230810 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0014270 decreased ovary secretion IAGP N RGD:5509061 20230810 MGI PMID:11145748 10870 Lhcgr luteinizing hormone/choriogonadotropin receptor gene MP:0031379 ambiguous external female genitalia IAGP N RGD:5509061 20220421 MGI PMID:11145749 10871 Lipc lipase, hepatic gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7852377 10871 Lipc lipase, hepatic gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16368783 10871 Lipc lipase, hepatic gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:11906928 10871 Lipc lipase, hepatic gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:16368783 10871 Lipc lipase, hepatic gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17431181 10871 Lipc lipase, hepatic gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16368783 10871 Lipc lipase, hepatic gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7852377 10871 Lipc lipase, hepatic gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:11906928 10871 Lipc lipase, hepatic gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11906928 10871 Lipc lipase, hepatic gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:16368783 10871 Lipc lipase, hepatic gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:11906928 10871 Lipc lipase, hepatic gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16368783 10871 Lipc lipase, hepatic gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17431181 10871 Lipc lipase, hepatic gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7852377 10871 Lipc lipase, hepatic gene MP:0006084 abnormal circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:7852377 10872 Lipe lipase, hormone sensitive gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11316346 10872 Lipe lipase, hormone sensitive gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:11316346 10872 Lipe lipase, hormone sensitive gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 10872 Lipe lipase, hormone sensitive gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11316346 10872 Lipe lipase, hormone sensitive gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11717312 10872 Lipe lipase, hormone sensitive gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 10872 Lipe lipase, hormone sensitive gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 10872 Lipe lipase, hormone sensitive gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:10639158 10872 Lipe lipase, hormone sensitive gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:10639158 10872 Lipe lipase, hormone sensitive gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18335062 10872 Lipe lipase, hormone sensitive gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 10872 Lipe lipase, hormone sensitive gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:11717312 10872 Lipe lipase, hormone sensitive gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19723498 10872 Lipe lipase, hormone sensitive gene MP:0001553 abnormal circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:11316346 10872 Lipe lipase, hormone sensitive gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19723498 10872 Lipe lipase, hormone sensitive gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12835327 10872 Lipe lipase, hormone sensitive gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18335062 10872 Lipe lipase, hormone sensitive gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11564684 10872 Lipe lipase, hormone sensitive gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10639158 10872 Lipe lipase, hormone sensitive gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11564684 10872 Lipe lipase, hormone sensitive gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12835327 10872 Lipe lipase, hormone sensitive gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11564684 10872 Lipe lipase, hormone sensitive gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19023560 10872 Lipe lipase, hormone sensitive gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12835327 10872 Lipe lipase, hormone sensitive gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16199803 10872 Lipe lipase, hormone sensitive gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:11564684 10872 Lipe lipase, hormone sensitive gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12865325 10872 Lipe lipase, hormone sensitive gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10639158 10872 Lipe lipase, hormone sensitive gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10639158 10872 Lipe lipase, hormone sensitive gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12835327 10872 Lipe lipase, hormone sensitive gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:10639158 10872 Lipe lipase, hormone sensitive gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12865325 10872 Lipe lipase, hormone sensitive gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12865325 10872 Lipe lipase, hormone sensitive gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10639158 10872 Lipe lipase, hormone sensitive gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10639158 10872 Lipe lipase, hormone sensitive gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:10639158 10872 Lipe lipase, hormone sensitive gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19023560 10872 Lipe lipase, hormone sensitive gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 10872 Lipe lipase, hormone sensitive gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19023560 10872 Lipe lipase, hormone sensitive gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11564684 10872 Lipe lipase, hormone sensitive gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:11564684 10872 Lipe lipase, hormone sensitive gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:11564684 10872 Lipe lipase, hormone sensitive gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19723498 10872 Lipe lipase, hormone sensitive gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19023560 10872 Lipe lipase, hormone sensitive gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:11717312 10872 Lipe lipase, hormone sensitive gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19723498 10872 Lipe lipase, hormone sensitive gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:11717312 10872 Lipe lipase, hormone sensitive gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:18335062 10872 Lipe lipase, hormone sensitive gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19023560 10872 Lipe lipase, hormone sensitive gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10639158 10872 Lipe lipase, hormone sensitive gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11717312 10872 Lipe lipase, hormone sensitive gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12835327 10872 Lipe lipase, hormone sensitive gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19723498 10872 Lipe lipase, hormone sensitive gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:19023560 10872 Lipe lipase, hormone sensitive gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12835327 10872 Lipe lipase, hormone sensitive gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11316346 10872 Lipe lipase, hormone sensitive gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12865325 10872 Lipe lipase, hormone sensitive gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19023560 10872 Lipe lipase, hormone sensitive gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19723498 10872 Lipe lipase, hormone sensitive gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:10639158 10872 Lipe lipase, hormone sensitive gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:18335062 10872 Lipe lipase, hormone sensitive gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:12835327 10872 Lipe lipase, hormone sensitive gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11316346 10872 Lipe lipase, hormone sensitive gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18335062 10872 Lipe lipase, hormone sensitive gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19023560 10872 Lipe lipase, hormone sensitive gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:10639158 10872 Lipe lipase, hormone sensitive gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:11717312 10872 Lipe lipase, hormone sensitive gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:10639158 10872 Lipe lipase, hormone sensitive gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:11564684 10872 Lipe lipase, hormone sensitive gene MP:0008032 abnormal lipolysis IAGP N RGD:5509061 20141003 MGI PMID:12835327 10872 Lipe lipase, hormone sensitive gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18335062 10872 Lipe lipase, hormone sensitive gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:12835327 10872 Lipe lipase, hormone sensitive gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:19023560 10872 Lipe lipase, hormone sensitive gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11316346 10872 Lipe lipase, hormone sensitive gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18335062 10872 Lipe lipase, hormone sensitive gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11316346 10872 Lipe lipase, hormone sensitive gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11717312 10872 Lipe lipase, hormone sensitive gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12865325 10872 Lipe lipase, hormone sensitive gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20191226 MGI PMID:16199803 10872 Lipe lipase, hormone sensitive gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:11717312 10872 Lipe lipase, hormone sensitive gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10639158 10872 Lipe lipase, hormone sensitive gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11564684 10872 Lipe lipase, hormone sensitive gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:18335062 10872 Lipe lipase, hormone sensitive gene MP:0014476 abnormal feces lipid level IAGP N RGD:5509061 20240704 MGI PMID:18335062 10872 Lipe lipase, hormone sensitive gene MP:0020101 abnormal hepatic glucose production IAGP N RGD:5509061 20190815 MGI PMID:12865325 10872 Lipe lipase, hormone sensitive gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:12865325 10872 Lipe lipase, hormone sensitive gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:18335062 10872 Lipe lipase, hormone sensitive gene MP:0031417 decreased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:11717312 10872 Lipe lipase, hormone sensitive gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:12835327 10876 Lpl lipoprotein lipase gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19481534 10876 Lpl lipoprotein lipase gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7759497 10876 Lpl lipoprotein lipase gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20170907 MGI PMID:12569168 10876 Lpl lipoprotein lipase gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170907 MGI PMID:12569168 10876 Lpl lipoprotein lipase gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170907 MGI PMID:12569168 10876 Lpl lipoprotein lipase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:7759497 10876 Lpl lipoprotein lipase gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18344982 10876 Lpl lipoprotein lipase gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16410253 10876 Lpl lipoprotein lipase gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20170907 MGI PMID:12569168 10876 Lpl lipoprotein lipase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:15028738 10876 Lpl lipoprotein lipase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20170907 MGI PMID:12569168 10876 Lpl lipoprotein lipase gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:19481534 10876 Lpl lipoprotein lipase gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:7759497 10876 Lpl lipoprotein lipase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16410253 10876 Lpl lipoprotein lipase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19481534 10876 Lpl lipoprotein lipase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:7759497 10876 Lpl lipoprotein lipase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:15028738 10876 Lpl lipoprotein lipase gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7759497 10876 Lpl lipoprotein lipase gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20170907 MGI PMID:12569168 10876 Lpl lipoprotein lipase gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15028738 10876 Lpl lipoprotein lipase gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16410253 10876 Lpl lipoprotein lipase gene MP:0002083 premature death IAGP N RGD:5509061 20170907 MGI PMID:12569168 10876 Lpl lipoprotein lipase gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7759497 10876 Lpl lipoprotein lipase gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20170907 MGI PMID:12569168 10876 Lpl lipoprotein lipase gene MP:0002833 increased heart weight IAGP N RGD:5509061 20170907 MGI PMID:12569168 10876 Lpl lipoprotein lipase gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16410253 10876 Lpl lipoprotein lipase gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:16410253 10876 Lpl lipoprotein lipase gene MP:0003820 increased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:16410253 10876 Lpl lipoprotein lipase gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:19481534 10876 Lpl lipoprotein lipase gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:7759497 10876 Lpl lipoprotein lipase gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:15028738 10876 Lpl lipoprotein lipase gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:7759497 10876 Lpl lipoprotein lipase gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18344982 10876 Lpl lipoprotein lipase gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:19481534 10876 Lpl lipoprotein lipase gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19481534 10876 Lpl lipoprotein lipase gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7759497 10876 Lpl lipoprotein lipase gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20170907 MGI PMID:12569168 10876 Lpl lipoprotein lipase gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20220630 MGI PMID:15028738 10876 Lpl lipoprotein lipase gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18344982 10876 Lpl lipoprotein lipase gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20170907 MGI PMID:12569168 10876 Lpl lipoprotein lipase gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16410253 10876 Lpl lipoprotein lipase gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18344982 10876 Lpl lipoprotein lipase gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20170907 MGI PMID:12569168 10876 Lpl lipoprotein lipase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16410253 10876 Lpl lipoprotein lipase gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:7759497 10876 Lpl lipoprotein lipase gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:7759497 10876 Lpl lipoprotein lipase gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20170907 MGI PMID:12569168 10876 Lpl lipoprotein lipase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7759497 10876 Lpl lipoprotein lipase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8675619 10876 Lpl lipoprotein lipase gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:15028738 10876 Lpl lipoprotein lipase gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:16410253 10876 Lpl lipoprotein lipase gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:19481534 10876 Lpl lipoprotein lipase gene MP:0031417 decreased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:15028738 10876 Lpl lipoprotein lipase gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:12569168 10876 Lpl lipoprotein lipase gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:16410253 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:7862670 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:7862670 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:7862670 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7862670 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:7862670 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:9184108 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:7862670 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:7862670 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:8922669 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7862670 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:7862670 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:7862670 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:8922669 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:7862670 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0003104 acrania IAGP N RGD:5509061 20141003 MGI PMID:8922669 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0008221 abnormal hippocampal commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:7862670 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:7862670 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7862670 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20141003 MGI PMID:9184108 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:7862670 10881 Marcks myristoylated alanine rich protein kinase C substrate gene MP:0030178 abnormal scalp morphology IAGP N RGD:5509061 20171214 MGI PMID:8922669 10882 Mal myelin and lymphocyte protein, T cell differentiation protein gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15337780 10882 Mal myelin and lymphocyte protein, T cell differentiation protein gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15337780 10883 Mat1a methionine adenosyltransferase 1A gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11320206 10883 Mat1a methionine adenosyltransferase 1A gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:11320206 10883 Mat1a methionine adenosyltransferase 1A gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11320206 10883 Mat1a methionine adenosyltransferase 1A gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:11320206 10883 Mat1a methionine adenosyltransferase 1A gene MP:0030644 increased circulating methionine level IAGP N RGD:5509061 20180920 MGI PMID:11320206 10883 Mat1a methionine adenosyltransferase 1A gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:11320206 10886 Mc5r melanocortin 5 receptor gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:9413988 10886 Mc5r melanocortin 5 receptor gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 10886 Mc5r melanocortin 5 receptor gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 10886 Mc5r melanocortin 5 receptor gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 10886 Mc5r melanocortin 5 receptor gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 10886 Mc5r melanocortin 5 receptor gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 10886 Mc5r melanocortin 5 receptor gene MP:0001348 abnormal lacrimal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:9413988 10886 Mc5r melanocortin 5 receptor gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230119 MGI 10886 Mc5r melanocortin 5 receptor gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 10886 Mc5r melanocortin 5 receptor gene MP:0002992 abnormal sebaceous lipid secretion IAGP N RGD:5509061 20141003 MGI PMID:9413988 10886 Mc5r melanocortin 5 receptor gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:14733892 10886 Mc5r melanocortin 5 receptor gene MP:0005238 increased brain size IEA N RGD:5509061 20230119 MGI 10886 Mc5r melanocortin 5 receptor gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:9413988 10886 Mc5r melanocortin 5 receptor gene MP:0013476 abnormal Harderian gland porphyrin secretion IAGP N RGD:5509061 20150212 MGI PMID:9413988 10890 Me1 malic enzyme 1, NADP(+)-dependent, cytosolic gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 10890 Me1 malic enzyme 1, NADP(+)-dependent, cytosolic gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19270708 10890 Me1 malic enzyme 1, NADP(+)-dependent, cytosolic gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200402 MGI 10890 Me1 malic enzyme 1, NADP(+)-dependent, cytosolic gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 10890 Me1 malic enzyme 1, NADP(+)-dependent, cytosolic gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:19270708 10890 Me1 malic enzyme 1, NADP(+)-dependent, cytosolic gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:7276516 10890 Me1 malic enzyme 1, NADP(+)-dependent, cytosolic gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 10891 Vps35 VPS35 retromer complex component gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 10891 Vps35 VPS35 retromer complex component gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20151119 MGI PMID:26203154 10891 Vps35 VPS35 retromer complex component gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20221117 MGI PMID:33745227 10891 Vps35 VPS35 retromer complex component gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20230511 MGI PMID:33257649 10891 Vps35 VPS35 retromer complex component gene MP:0001405 impaired coordination IAGP N RGD:5509061 20221117 MGI PMID:33745227 10891 Vps35 VPS35 retromer complex component gene MP:0001406 abnormal gait IEA N RGD:5509061 20200514 MGI 10891 Vps35 VPS35 retromer complex component gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:22105352 10891 Vps35 VPS35 retromer complex component gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22105352 10891 Vps35 VPS35 retromer complex component gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:22105352 10891 Vps35 VPS35 retromer complex component gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22105352 10891 Vps35 VPS35 retromer complex component gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 10891 Vps35 VPS35 retromer complex component gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20221117 MGI PMID:33745227 10891 Vps35 VPS35 retromer complex component gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20151119 MGI PMID:26203154 10891 Vps35 VPS35 retromer complex component gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:22105352 10891 Vps35 VPS35 retromer complex component gene MP:0002922 decreased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:22105352 10891 Vps35 VPS35 retromer complex component gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20200827 MGI PMID:31771656 10891 Vps35 VPS35 retromer complex component gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20151119 MGI PMID:26203154 10891 Vps35 VPS35 retromer complex component gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20221117 MGI PMID:33745227 10891 Vps35 VPS35 retromer complex component gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20151119 MGI PMID:26203154 10891 Vps35 VPS35 retromer complex component gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:22105352 10891 Vps35 VPS35 retromer complex component gene MP:0003354 astrocytosis IAGP N RGD:5509061 20221117 MGI PMID:33745227 10891 Vps35 VPS35 retromer complex component gene MP:0003674 oxidative stress IAGP N RGD:5509061 20230511 MGI PMID:33257649 10891 Vps35 VPS35 retromer complex component gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22105352 10891 Vps35 VPS35 retromer complex component gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20151119 MGI PMID:26203154 10891 Vps35 VPS35 retromer complex component gene MP:0005156 bradykinesia IAGP N RGD:5509061 20230511 MGI PMID:33257649 10891 Vps35 VPS35 retromer complex component gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20221117 MGI PMID:33745227 10891 Vps35 VPS35 retromer complex component gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20200827 MGI PMID:31771656 10891 Vps35 VPS35 retromer complex component gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20151119 MGI PMID:26203154 10891 Vps35 VPS35 retromer complex component gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20221117 MGI PMID:33745227 10891 Vps35 VPS35 retromer complex component gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20200827 MGI PMID:31771656 10891 Vps35 VPS35 retromer complex component gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20151119 MGI PMID:26203154 10891 Vps35 VPS35 retromer complex component gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20221117 MGI PMID:33745227 10891 Vps35 VPS35 retromer complex component gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20200827 MGI PMID:31771656 10891 Vps35 VPS35 retromer complex component gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200827 MGI PMID:31771656 10891 Vps35 VPS35 retromer complex component gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20200827 MGI PMID:31771656 10891 Vps35 VPS35 retromer complex component gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20200827 MGI PMID:31771656 10891 Vps35 VPS35 retromer complex component gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20200827 MGI PMID:31771656 10891 Vps35 VPS35 retromer complex component gene MP:0008837 increased transforming growth factor beta level IAGP N RGD:5509061 20200827 MGI PMID:31771656 10891 Vps35 VPS35 retromer complex component gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20221117 MGI PMID:33745227 10891 Vps35 VPS35 retromer complex component gene MP:0008918 microgliosis IAGP N RGD:5509061 20200827 MGI PMID:31771656 10891 Vps35 VPS35 retromer complex component gene MP:0008918 microgliosis IAGP N RGD:5509061 20221117 MGI PMID:33745227 10891 Vps35 VPS35 retromer complex component gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200827 MGI PMID:31771656 10891 Vps35 VPS35 retromer complex component gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20160304 MGI PMID:24130821 10891 Vps35 VPS35 retromer complex component gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22105352 10891 Vps35 VPS35 retromer complex component gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22105352 10891 Vps35 VPS35 retromer complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10891 Vps35 VPS35 retromer complex component gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20221117 MGI PMID:33745227 10891 Vps35 VPS35 retromer complex component gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20230511 MGI PMID:33257649 10891 Vps35 VPS35 retromer complex component gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20221117 MGI PMID:33745227 10891 Vps35 VPS35 retromer complex component gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20230511 MGI PMID:33257649 10891 Vps35 VPS35 retromer complex component gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20230511 MGI PMID:33257649 10891 Vps35 VPS35 retromer complex component gene MP:0020211 slow movement IAGP N RGD:5509061 20230511 MGI PMID:33257649 10891 Vps35 VPS35 retromer complex component gene MP:0020874 abnormal nervous system dopamine level IAGP N RGD:5509061 20221117 MGI PMID:30155515 10892 Mep1a meprin 1 alpha gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18971209 10892 Mep1a meprin 1 alpha gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19262505 10892 Mep1a meprin 1 alpha gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18971209 10892 Mep1a meprin 1 alpha gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18971209 10892 Mep1a meprin 1 alpha gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 10892 Mep1a meprin 1 alpha gene MP:0005265 abnormal blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18971209 10892 Mep1a meprin 1 alpha gene MP:0005328 abnormal circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:18971209 10892 Mep1a meprin 1 alpha gene MP:0005502 abnormal renal/urinary system physiology IAGP N RGD:5509061 20141003 MGI PMID:18971209 10892 Mep1a meprin 1 alpha gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:19262505 10892 Mep1a meprin 1 alpha gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:19262505 10892 Mep1a meprin 1 alpha gene MP:0008640 abnormal circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:18971209 10892 Mep1a meprin 1 alpha gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:19262505 10892 Mep1a meprin 1 alpha gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18971209 10892 Mep1a meprin 1 alpha gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:19262505 10892 Mep1a meprin 1 alpha gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:19262505 10892 Mep1a meprin 1 alpha gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:18971209 10892 Mep1a meprin 1 alpha gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18971209 10892 Mep1a meprin 1 alpha gene MP:0009646 urinary bladder inflammation IAGP N RGD:5509061 20141003 MGI PMID:18971209 10892 Mep1a meprin 1 alpha gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 10892 Mep1a meprin 1 alpha gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 10892 Mep1a meprin 1 alpha gene MP:0011352 proximal convoluted tubule brush border loss IAGP N RGD:5509061 20141003 MGI PMID:18971209 10892 Mep1a meprin 1 alpha gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 10893 Mep1b meprin 1 beta gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12556482 10893 Mep1b meprin 1 beta gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 10893 Mep1b meprin 1 beta gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18172000 10893 Mep1b meprin 1 beta gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12556482 10893 Mep1b meprin 1 beta gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:18172000 10893 Mep1b meprin 1 beta gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:18172000 10893 Mep1b meprin 1 beta gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18172000 10893 Mep1b meprin 1 beta gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18971209 10893 Mep1b meprin 1 beta gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18172000 10893 Mep1b meprin 1 beta gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12556482 10893 Mep1b meprin 1 beta gene MP:0011352 proximal convoluted tubule brush border loss IAGP N RGD:5509061 20141003 MGI PMID:18172000 10894 Met met proto-oncogene gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:15557554 10894 Met met proto-oncogene gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12397180 10894 Met met proto-oncogene gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:8898205 10894 Met met proto-oncogene gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:11430831 10894 Met met proto-oncogene gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:15070743 10894 Met met proto-oncogene gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:7651534 10894 Met met proto-oncogene gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:11430831 10894 Met met proto-oncogene gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:11430831 10894 Met met proto-oncogene gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:7651534 10894 Met met proto-oncogene gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:8898205 10894 Met met proto-oncogene gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:12388344 10894 Met met proto-oncogene gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:7651534 10894 Met met proto-oncogene gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20240808 MGI PMID:38438594 10894 Met met proto-oncogene gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:12397180 10894 Met met proto-oncogene gene MP:0000860 abnormal primary somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21195751 10894 Met met proto-oncogene gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:21813676 10894 Met met proto-oncogene gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:11430831 10894 Met met proto-oncogene gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:21813676 10894 Met met proto-oncogene gene MP:0001051 abnormal somatic motor system morphology IAGP N RGD:5509061 20141003 MGI PMID:11430831 10894 Met met proto-oncogene gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:21813676 10894 Met met proto-oncogene gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17923692 10894 Met met proto-oncogene gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17583691 10894 Met met proto-oncogene gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20180927 MGI PMID:29999500 10894 Met met proto-oncogene gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12397180 10894 Met met proto-oncogene gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21813676 10894 Met met proto-oncogene gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8898205 10894 Met met proto-oncogene gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:7651534 10894 Met met proto-oncogene gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:10995442 10894 Met met proto-oncogene gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10995442 10894 Met met proto-oncogene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8898205 10894 Met met proto-oncogene gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:15070743 10894 Met met proto-oncogene gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19567831 10894 Met met proto-oncogene gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11430831 10894 Met met proto-oncogene gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:8898205 10894 Met met proto-oncogene gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17923692 10894 Met met proto-oncogene gene MP:0001958 emphysema IAGP N RGD:5509061 20180927 MGI PMID:29999500 10894 Met met proto-oncogene gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15557554 10894 Met met proto-oncogene gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15557554 10894 Met met proto-oncogene gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19567831 10894 Met met proto-oncogene gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15557554 10894 Met met proto-oncogene gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:21195751 10894 Met met proto-oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15557554 10894 Met met proto-oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11430831 10894 Met met proto-oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15070743 10894 Met met proto-oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8898205 10894 Met met proto-oncogene gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20180927 MGI PMID:29999500 10894 Met met proto-oncogene gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:11430831 10894 Met met proto-oncogene gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:12388344 10894 Met met proto-oncogene gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22427375 10894 Met met proto-oncogene gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:15557554 10894 Met met proto-oncogene gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:22427375 10894 Met met proto-oncogene gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:12388344 10894 Met met proto-oncogene gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:7651534 10894 Met met proto-oncogene gene MP:0003326 liver failure IAGP N RGD:5509061 20141003 MGI PMID:15070743 10894 Met met proto-oncogene gene MP:0003359 hypaxial muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10995442 10894 Met met proto-oncogene gene MP:0003359 hypaxial muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12388344 10894 Met met proto-oncogene gene MP:0003359 hypaxial muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7651534 10894 Met met proto-oncogene gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:10995442 10894 Met met proto-oncogene gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:11430831 10894 Met met proto-oncogene gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22427375 10894 Met met proto-oncogene gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:21813676 10894 Met met proto-oncogene gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15557554 10894 Met met proto-oncogene gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19567831 10894 Met met proto-oncogene gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15070743 10894 Met met proto-oncogene gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15070743 10894 Met met proto-oncogene gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:12388344 10894 Met met proto-oncogene gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:15557554 10894 Met met proto-oncogene gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:21195751 10894 Met met proto-oncogene gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21195751 10894 Met met proto-oncogene gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8898205 10894 Met met proto-oncogene gene MP:0004170 abnormal orbitofrontal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21195751 10894 Met met proto-oncogene gene MP:0004197 abnormal fetal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:11430831 10894 Met met proto-oncogene gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:7651534 10894 Met met proto-oncogene gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15557554 10894 Met met proto-oncogene gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19567831 10894 Met met proto-oncogene gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:11430831 10894 Met met proto-oncogene gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:8898205 10894 Met met proto-oncogene gene MP:0004266 pale placenta IAGP N RGD:5509061 20141003 MGI PMID:8898205 10894 Met met proto-oncogene gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17923692 10894 Met met proto-oncogene gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21813676 10894 Met met proto-oncogene gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:11430831 10894 Met met proto-oncogene gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:8898205 10894 Met met proto-oncogene gene MP:0004846 absent skeletal muscle IAGP N RGD:5509061 20141003 MGI PMID:15653949 10894 Met met proto-oncogene gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:15070743 10894 Met met proto-oncogene gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:22427375 10894 Met met proto-oncogene gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22427375 10894 Met met proto-oncogene gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:15070743 10894 Met met proto-oncogene gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:15249655 10894 Met met proto-oncogene gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22427375 10894 Met met proto-oncogene gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:7651534 10894 Met met proto-oncogene gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:22427375 10894 Met met proto-oncogene gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15557554 10894 Met met proto-oncogene gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:8898205 10894 Met met proto-oncogene gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17923692 10894 Met met proto-oncogene gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20240808 MGI PMID:38438594 10894 Met met proto-oncogene gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21195751 10894 Met met proto-oncogene gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:12397180 10894 Met met proto-oncogene gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:17881575 10894 Met met proto-oncogene gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20141003 MGI PMID:7651534 10894 Met met proto-oncogene gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:12397180 10894 Met met proto-oncogene gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15070743 10894 Met met proto-oncogene gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9331067 10894 Met met proto-oncogene gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19567831 10894 Met met proto-oncogene gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:17923692 10894 Met met proto-oncogene gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:17583691 10894 Met met proto-oncogene gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17923692 10894 Met met proto-oncogene gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11430831 10894 Met met proto-oncogene gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12397180 10894 Met met proto-oncogene gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8898205 10894 Met met proto-oncogene gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17923692 10894 Met met proto-oncogene gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15070743 10894 Met met proto-oncogene gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15557554 10894 Met met proto-oncogene gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15557554 10894 Met met proto-oncogene gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11430831 10894 Met met proto-oncogene gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7651534 10894 Met met proto-oncogene gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8898205 10894 Met met proto-oncogene gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22427375 10894 Met met proto-oncogene gene MP:0011883 absent diaphragm IAGP N RGD:5509061 20141003 MGI PMID:8898205 10894 Met met proto-oncogene gene MP:0012043 increased myoepithelioma incidence IAGP N RGD:5509061 20141003 MGI PMID:19567831 10894 Met met proto-oncogene gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20141003 MGI PMID:7651534 10894 Met met proto-oncogene gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15557554 10894 Met met proto-oncogene gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:17923692 10894 Met met proto-oncogene gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20160915 MGI PMID:15070743 10894 Met met proto-oncogene gene MP:0030208 abnormal intrinsic tongue muscle morphology IAGP N RGD:5509061 20171026 MGI PMID:7651534 10894 Met met proto-oncogene gene MP:0030945 abnormal myoblast migration IAGP N RGD:5509061 20190725 MGI PMID:11430831 10894 Met met proto-oncogene gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:15249655 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:15155946 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15155946 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15834428 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16195353 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17638889 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15155946 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17638889 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:15155946 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:15834428 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:16195353 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:22723547 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:16275924 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12941270 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15834428 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:16195353 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:19240116 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12941270 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17638889 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:15834428 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:19240116 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:17638889 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:17638889 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:19240116 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:15834428 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:16275924 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:22723547 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20151119 MGI PMID:23443560 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:22723547 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0004934 epididymis epithelium degeneration IAGP N RGD:5509061 20141003 MGI PMID:19240116 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:15155946 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:16275924 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:16195353 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:16275924 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0008119 decreased Langerhans cell number IAGP N RGD:5509061 20141003 MGI PMID:17638889 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:15155946 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16195353 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0009824 spermatic granuloma IAGP N RGD:5509061 20141003 MGI PMID:19240116 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17638889 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0013148 mastitis IAGP N RGD:5509061 20150730 MGI PMID:16195353 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0013716 hypolactation IAGP N RGD:5509061 20150611 MGI PMID:16275924 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0014347 increased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:15155946 10895 Mfge8 milk fat globule EGF and factor V/VIII domain containing gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:12941270 10896 Mgmt O-6-methylguanine-DNA methyltransferase gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9560238 10896 Mgmt O-6-methylguanine-DNA methyltransferase gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9560238 10896 Mgmt O-6-methylguanine-DNA methyltransferase gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:17098815 10896 Mgmt O-6-methylguanine-DNA methyltransferase gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17098815 10896 Mgmt O-6-methylguanine-DNA methyltransferase gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9560238 10896 Mgmt O-6-methylguanine-DNA methyltransferase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 10896 Mgmt O-6-methylguanine-DNA methyltransferase gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:17098815 10896 Mgmt O-6-methylguanine-DNA methyltransferase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9560238 10898 Mip major intrinsic protein of lens fiber gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:12676560 10898 Mip major intrinsic protein of lens fiber gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:7333462 10898 Mip major intrinsic protein of lens fiber gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:11773604 10898 Mip major intrinsic protein of lens fiber gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:11773604 10898 Mip major intrinsic protein of lens fiber gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:12676560 10898 Mip major intrinsic protein of lens fiber gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:5786866 10898 Mip major intrinsic protein of lens fiber gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:7333462 10898 Mip major intrinsic protein of lens fiber gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:5786866 10898 Mip major intrinsic protein of lens fiber gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:7333462 10898 Mip major intrinsic protein of lens fiber gene MP:0001309 hydropic eye lens fibers IEA N RGD:5509061 20111116 MGI 10898 Mip major intrinsic protein of lens fiber gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:1026873 10898 Mip major intrinsic protein of lens fiber gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12676560 10898 Mip major intrinsic protein of lens fiber gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:5716581 10898 Mip major intrinsic protein of lens fiber gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:5786866 10898 Mip major intrinsic protein of lens fiber gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:7333462 10898 Mip major intrinsic protein of lens fiber gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12676560 10898 Mip major intrinsic protein of lens fiber gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:11773604 10898 Mip major intrinsic protein of lens fiber gene MP:0005545 abnormal lens development IEA N RGD:5509061 20141003 MGI 10898 Mip major intrinsic protein of lens fiber gene MP:0010263 total cataract IAGP N RGD:5509061 20141003 MGI PMID:7333462 10898 Mip major intrinsic protein of lens fiber gene MP:0011697 lens vacuoles IEA N RGD:5509061 20141003 MGI 10898 Mip major intrinsic protein of lens fiber gene MP:0031345 developmental cataract IAGP N RGD:5509061 20220217 MGI PMID:12676560 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000017 big ears IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:16618927 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:7477409 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15635450 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22674806 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:18371366 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000448 pointed snout IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:18371367 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:10393173 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:22516260 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:24122813 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21670200 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:12781363 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:15635450 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10393173 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12781363 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15635450 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16096649 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22516260 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22674806 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:24122813 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:24122813 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:19212323 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:19212323 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11536426 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:11536426 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23934123 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19212323 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:21670200 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15635450 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22674806 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7477409 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16981007 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:15635450 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19212323 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7477409 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:21670200 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:24040009 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21670200 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:24040009 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:7477409 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:15635450 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16096649 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:10393173 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:12781363 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:16096649 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:18977325 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:22674806 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:24122813 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10393173 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12781363 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18371366 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19212323 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22516260 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22674806 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24122813 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10393173 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18371366 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24040009 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24122813 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19212323 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:16096649 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:16096649 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:24040009 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:15635450 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:16981007 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21670200 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:19212323 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:11536426 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:7477409 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7477409 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11536426 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16981007 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7477409 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11536426 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:16981007 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:15635450 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:22674806 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:7477409 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:16981007 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:7477409 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004049 increased acute promyelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:22516260 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:19212323 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004569 glossopharyngeal nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23934123 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11536426 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:11536426 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:11536426 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:16618927 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16618927 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7477409 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11536426 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7477409 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16981007 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11536426 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16981007 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7477409 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:11536426 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18371366 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18371367 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18371366 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18371367 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21670200 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:24040009 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:10393173 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:12781363 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:19212323 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:7477409 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16981007 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0005649 increased spleen neoplasm incidence IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:19212323 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16981007 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21670200 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16981007 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18371367 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18371366 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:15635450 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18371366 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18371367 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21670200 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18371366 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18371367 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:7477409 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0009879 abnormal arcus anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:16618927 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0009879 abnormal arcus anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:23934123 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19212323 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:23934123 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16096649 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15635450 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22516260 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:24122813 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21670200 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16981007 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18977325 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18371366 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24040009 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7477409 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11536426 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18371366 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21670200 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18371367 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:22674806 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:16951254 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:23934123 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0012284 increased sternebra number IAGP N RGD:5509061 20141003 MGI PMID:16618927 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0013176 abnormal tail position or orientation IAGP N RGD:5509061 20141003 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0030066 short face IAGP N RGD:5509061 20170921 MGI PMID:16551973 10900 Kmt2a lysine (K)-specific methyltransferase 2A gene MP:0030956 abnormal neuronal precursor cell migration IAGP N RGD:5509061 20190725 MGI PMID:19212323 10905 Mmp11 matrix metallopeptidase 11 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 10905 Mmp11 matrix metallopeptidase 11 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:14522908 10905 Mmp11 matrix metallopeptidase 11 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14522908 10905 Mmp11 matrix metallopeptidase 11 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20181227 MGI 10905 Mmp11 matrix metallopeptidase 11 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:14522908 10905 Mmp11 matrix metallopeptidase 11 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:9508784 10905 Mmp11 matrix metallopeptidase 11 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:10591662 10905 Mmp11 matrix metallopeptidase 11 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 10905 Mmp11 matrix metallopeptidase 11 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 10905 Mmp11 matrix metallopeptidase 11 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 10905 Mmp11 matrix metallopeptidase 11 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14522908 10905 Mmp11 matrix metallopeptidase 11 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20181227 MGI 10905 Mmp11 matrix metallopeptidase 11 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 10906 Mmp7 matrix metallopeptidase 7 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:16769909 10906 Mmp7 matrix metallopeptidase 7 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:17617617 10906 Mmp7 matrix metallopeptidase 7 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17617617 10906 Mmp7 matrix metallopeptidase 7 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:9769324 10906 Mmp7 matrix metallopeptidase 7 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16397239 10906 Mmp7 matrix metallopeptidase 7 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9037065 10906 Mmp7 matrix metallopeptidase 7 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19002110 10906 Mmp7 matrix metallopeptidase 7 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15618213 10906 Mmp7 matrix metallopeptidase 7 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17923522 10906 Mmp7 matrix metallopeptidase 7 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10642592 10906 Mmp7 matrix metallopeptidase 7 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:19002110 10906 Mmp7 matrix metallopeptidase 7 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:9037065 10906 Mmp7 matrix metallopeptidase 7 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10642592 10906 Mmp7 matrix metallopeptidase 7 gene MP:0003901 abnormal PR interval IAGP N RGD:5509061 20141003 MGI PMID:16769909 10906 Mmp7 matrix metallopeptidase 7 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:17617617 10906 Mmp7 matrix metallopeptidase 7 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:12045257 10906 Mmp7 matrix metallopeptidase 7 gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:16769909 10906 Mmp7 matrix metallopeptidase 7 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:17617617 10906 Mmp7 matrix metallopeptidase 7 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:10642592 10906 Mmp7 matrix metallopeptidase 7 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:17617617 10906 Mmp7 matrix metallopeptidase 7 gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:12506066 10906 Mmp7 matrix metallopeptidase 7 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16769909 10906 Mmp7 matrix metallopeptidase 7 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17617617 10906 Mmp7 matrix metallopeptidase 7 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18676849 10908 Mobp myelin-associated oligodendrocytic basic protein gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:10103078 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15908920 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:18641296 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:19483694 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:15908920 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:15908920 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:18641296 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:19483694 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18641296 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:19483694 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15908920 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18641296 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18641296 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19483694 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18641296 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:18641296 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:15908920 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:18641296 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15908920 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:14624757 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15908920 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:15908920 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:19483694 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:19483694 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:14624757 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:19483694 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12925695 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16237080 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21068410 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20150806 MGI PMID:19487416 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14624757 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:14624757 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:19483694 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:14624757 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:14624757 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0010205 abnormal oligodendrocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21068410 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0030987 spinal cord inflammation IAGP N RGD:5509061 20191128 MGI PMID:18641296 10909 Mog myelin oligodendrocyte glycoprotein gene MP:0030991 optic nerve inflammation IAGP N RGD:5509061 20191128 MGI PMID:18641296 10910 Mos Moloney sarcoma oncogene gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:8015609 10910 Mos Moloney sarcoma oncogene gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:8015610 10910 Mos Moloney sarcoma oncogene gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:8692939 10910 Mos Moloney sarcoma oncogene gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8015610 10910 Mos Moloney sarcoma oncogene gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8015609 10910 Mos Moloney sarcoma oncogene gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8015610 10910 Mos Moloney sarcoma oncogene gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:8015609 10910 Mos Moloney sarcoma oncogene gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8015610 10910 Mos Moloney sarcoma oncogene gene MP:0002833 increased heart weight IEA N RGD:5509061 20220811 MGI 10910 Mos Moloney sarcoma oncogene gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20221215 MGI 10910 Mos Moloney sarcoma oncogene gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:8015609 10910 Mos Moloney sarcoma oncogene gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:8015610 10910 Mos Moloney sarcoma oncogene gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:8692939 10910 Mos Moloney sarcoma oncogene gene MP:0009443 parthenogenesis IAGP N RGD:5509061 20141003 MGI PMID:8692939 10910 Mos Moloney sarcoma oncogene gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:11069114 10910 Mos Moloney sarcoma oncogene gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:8015609 10910 Mos Moloney sarcoma oncogene gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:8692939 10910 Mos Moloney sarcoma oncogene gene MP:0012736 abnormal polar body morphology IAGP N RGD:5509061 20141003 MGI PMID:8015609 10910 Mos Moloney sarcoma oncogene gene MP:0012737 abnormal primary polar body morphology IAGP N RGD:5509061 20141003 MGI PMID:8692939 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:17098815 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11463841 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:14633693 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:17098815 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:11463841 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11463841 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17098815 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17098815 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:11463841 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11463841 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11463841 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:14633693 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9742100 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:17098815 10914 Mpg N-methylpurine-DNA glycosylase gene MP:0009488 abnormal pancreatic islet cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11463841 10915 Mpi mannose phosphate isomerase gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:16339137 10915 Mpi mannose phosphate isomerase gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16339137 10915 Mpi mannose phosphate isomerase gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16339137 10915 Mpi mannose phosphate isomerase gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:16339137 10915 Mpi mannose phosphate isomerase gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:16339137 10915 Mpi mannose phosphate isomerase gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:16339137 10915 Mpi mannose phosphate isomerase gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:16339137 10915 Mpi mannose phosphate isomerase gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 10915 Mpi mannose phosphate isomerase gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16339137 10915 Mpi mannose phosphate isomerase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16339137 10915 Mpi mannose phosphate isomerase gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:16339137 10915 Mpi mannose phosphate isomerase gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:16339137 10915 Mpi mannose phosphate isomerase gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16339137 10915 Mpi mannose phosphate isomerase gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16339137 10915 Mpi mannose phosphate isomerase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16339137 10915 Mpi mannose phosphate isomerase gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20141003 MGI 10915 Mpi mannose phosphate isomerase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16339137 10915 Mpi mannose phosphate isomerase gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150219 MGI PMID:16339137 10916 Mpo myeloperoxidase gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11181641 10916 Mpo myeloperoxidase gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16266986 10916 Mpo myeloperoxidase gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:10085024 10916 Mpo myeloperoxidase gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:11181641 10916 Mpo myeloperoxidase gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:15790660 10916 Mpo myeloperoxidase gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15790660 10916 Mpo myeloperoxidase gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:11108938 10916 Mpo myeloperoxidase gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:11593004 10916 Mpo myeloperoxidase gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:15790660 10916 Mpo myeloperoxidase gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:10085024 10916 Mpo myeloperoxidase gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:11181641 10916 Mpo myeloperoxidase gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15911707 10916 Mpo myeloperoxidase gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:10085024 10916 Mpo myeloperoxidase gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:11181641 10916 Mpo myeloperoxidase gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16266986 10916 Mpo myeloperoxidase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11181641 10916 Mpo myeloperoxidase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11593004 10917 Mpz myelin protein zero gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12616486 10917 Mpz myelin protein zero gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:10632602 10917 Mpz myelin protein zero gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:1384988 10917 Mpz myelin protein zero gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:22219655 10917 Mpz myelin protein zero gene MP:0000745 tremors IAGP N RGD:5509061 20180809 MGI PMID:22689911 10917 Mpz myelin protein zero gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:1384988 10917 Mpz myelin protein zero gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:12616486 10917 Mpz myelin protein zero gene MP:0000755 hindlimb paralysis IEA N RGD:5509061 20111116 MGI 10917 Mpz myelin protein zero gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:10632602 10917 Mpz myelin protein zero gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:11266447 10917 Mpz myelin protein zero gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:7581451 10917 Mpz myelin protein zero gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20190221 MGI PMID:16495463 10917 Mpz myelin protein zero gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:18326085 10917 Mpz myelin protein zero gene MP:0000921 demyelination IAGP N RGD:5509061 20190221 MGI PMID:16495463 10917 Mpz myelin protein zero gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1384988 10917 Mpz myelin protein zero gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20180809 MGI PMID:22689911 10917 Mpz myelin protein zero gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20181227 MGI 10917 Mpz myelin protein zero gene MP:0001393 ataxia IAGP N RGD:5509061 20180809 MGI PMID:22689911 10917 Mpz myelin protein zero gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20181227 MGI 10917 Mpz myelin protein zero gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180809 MGI PMID:22689911 10917 Mpz myelin protein zero gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190124 MGI PMID:30239779 10917 Mpz myelin protein zero gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190221 MGI PMID:16495463 10917 Mpz myelin protein zero gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12616486 10917 Mpz myelin protein zero gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:1384988 10917 Mpz myelin protein zero gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22219655 10917 Mpz myelin protein zero gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:1384988 10917 Mpz myelin protein zero gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22219655 10917 Mpz myelin protein zero gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:1384988 10917 Mpz myelin protein zero gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:10632602 10917 Mpz myelin protein zero gene MP:0001924 infertility IEA N RGD:5509061 20111116 MGI 10917 Mpz myelin protein zero gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 10917 Mpz myelin protein zero gene MP:0001926 female infertility IEA N RGD:5509061 20111116 MGI 10917 Mpz myelin protein zero gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 10917 Mpz myelin protein zero gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 10917 Mpz myelin protein zero gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 10917 Mpz myelin protein zero gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20180809 MGI PMID:22689911 10917 Mpz myelin protein zero gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10632602 10917 Mpz myelin protein zero gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:12616486 10917 Mpz myelin protein zero gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:18326085 10917 Mpz myelin protein zero gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:1384988 10917 Mpz myelin protein zero gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:10632602 10917 Mpz myelin protein zero gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:10632602 10917 Mpz myelin protein zero gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:10632602 10917 Mpz myelin protein zero gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20180809 MGI PMID:22689911 10917 Mpz myelin protein zero gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20190221 MGI PMID:16495463 10917 Mpz myelin protein zero gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20190228 MGI PMID:11086005 10917 Mpz myelin protein zero gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18326085 10917 Mpz myelin protein zero gene MP:0004263 abnormal limb posture IEA N RGD:5509061 20181011 MGI 10917 Mpz myelin protein zero gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10632602 10917 Mpz myelin protein zero gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20180809 MGI PMID:22689911 10917 Mpz myelin protein zero gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20190221 MGI PMID:16495463 10917 Mpz myelin protein zero gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:10632602 10917 Mpz myelin protein zero gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:7581451 10917 Mpz myelin protein zero gene MP:0005405 axon degeneration IAGP N RGD:5509061 20190221 MGI PMID:16495463 10917 Mpz myelin protein zero gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18326085 10917 Mpz myelin protein zero gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:12616486 10917 Mpz myelin protein zero gene MP:0008243 abnormal macrophage derived foam cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18326085 10917 Mpz myelin protein zero gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18326085 10917 Mpz myelin protein zero gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:10632602 10917 Mpz myelin protein zero gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20180809 MGI PMID:22689911 10917 Mpz myelin protein zero gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20190221 MGI PMID:16495463 10917 Mpz myelin protein zero gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20190228 MGI PMID:11086005 10917 Mpz myelin protein zero gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 10917 Mpz myelin protein zero gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 10917 Mpz myelin protein zero gene MP:0010742 increased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:10632602 10917 Mpz myelin protein zero gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:11266447 10917 Mpz myelin protein zero gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20180809 MGI PMID:22689911 10917 Mpz myelin protein zero gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20190221 MGI PMID:16495463 10917 Mpz myelin protein zero gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20190228 MGI PMID:11086005 10917 Mpz myelin protein zero gene MP:0011906 increased Schwann cell proliferation IAGP N RGD:5509061 20180809 MGI PMID:22689911 10917 Mpz myelin protein zero gene MP:0012674 tomacula IAGP N RGD:5509061 20190228 MGI PMID:11086005 10917 Mpz myelin protein zero gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 10917 Mpz myelin protein zero gene MP:0013438 dysmyelination IAGP N RGD:5509061 20180809 MGI PMID:22689911 10917 Mpz myelin protein zero gene MP:0013438 dysmyelination IAGP N RGD:5509061 20190124 MGI PMID:30239779 10917 Mpz myelin protein zero gene MP:0013438 dysmyelination IAGP N RGD:5509061 20190221 MGI PMID:16495463 10917 Mpz myelin protein zero gene MP:0013438 dysmyelination IAGP N RGD:5509061 20190228 MGI PMID:11086005 10917 Mpz myelin protein zero gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20180809 MGI PMID:22689911 10917 Mpz myelin protein zero gene MP:0020452 abnormal axon radial sorting IAGP N RGD:5509061 20190124 MGI PMID:30239779 10918 Mras muscle and microspikes RAS gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20230601 MGI 10918 Mras muscle and microspikes RAS gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 10918 Mras muscle and microspikes RAS gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 10918 Mras muscle and microspikes RAS gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16980617 10918 Mras muscle and microspikes RAS gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20230601 MGI 10918 Mras muscle and microspikes RAS gene MP:0003960 increased lean body mass IEA N RGD:5509061 20230601 MGI 10918 Mras muscle and microspikes RAS gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 10918 Mras muscle and microspikes RAS gene MP:0005017 decreased B cell number IEA N RGD:5509061 20141003 MGI 10918 Mras muscle and microspikes RAS gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230119 MGI 10918 Mras muscle and microspikes RAS gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230601 MGI 10919 Abcc1 ATP-binding cassette, sub-family C member 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21881209 10919 Abcc1 ATP-binding cassette, sub-family C member 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9393741 10919 Abcc1 ATP-binding cassette, sub-family C member 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9359705 10919 Abcc1 ATP-binding cassette, sub-family C member 1 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9359705 10919 Abcc1 ATP-binding cassette, sub-family C member 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:21881209 10919 Abcc1 ATP-binding cassette, sub-family C member 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9359705 10919 Abcc1 ATP-binding cassette, sub-family C member 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9393741 10919 Abcc1 ATP-binding cassette, sub-family C member 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:21881209 10919 Abcc1 ATP-binding cassette, sub-family C member 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9359705 10921 Msx2 msh homeobox 2 gene MP:0000017 big ears IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:12701100 10921 Msx2 msh homeobox 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17654563 10921 Msx2 msh homeobox 2 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14597577 10921 Msx2 msh homeobox 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:18442049 10921 Msx2 msh homeobox 2 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000126 brittle teeth IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000127 degenerate molars IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000129 ameloblast degeneration IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20150903 MGI PMID:18667074 10921 Msx2 msh homeobox 2 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20150903 MGI PMID:18667074 10921 Msx2 msh homeobox 2 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:17654563 10921 Msx2 msh homeobox 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:18442049 10921 Msx2 msh homeobox 2 gene MP:0000423 delayed hair regrowth IEA N RGD:5509061 20141003 MGI 10921 Msx2 msh homeobox 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:18442049 10921 Msx2 msh homeobox 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:18442049 10921 Msx2 msh homeobox 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:15930102 10921 Msx2 msh homeobox 2 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15930102 10921 Msx2 msh homeobox 2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:14597577 10921 Msx2 msh homeobox 2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:15930102 10921 Msx2 msh homeobox 2 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:15930102 10921 Msx2 msh homeobox 2 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:15930102 10921 Msx2 msh homeobox 2 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:21387539 10921 Msx2 msh homeobox 2 gene MP:0000580 deformed nails IAGP N RGD:5509061 20141003 MGI PMID:21387539 10921 Msx2 msh homeobox 2 gene MP:0000583 long toenails IAGP N RGD:5509061 20141003 MGI PMID:21387539 10921 Msx2 msh homeobox 2 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:12874124 10921 Msx2 msh homeobox 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:18442049 10921 Msx2 msh homeobox 2 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000867 abnormal cerebellum anterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000870 absent cerebellum vermis lobule VIII IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000871 absent cerebellum vermis lobule IX IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000884 delaminated Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000887 delaminated cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12874124 10921 Msx2 msh homeobox 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18442049 10921 Msx2 msh homeobox 2 gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20150205 MGI PMID:24715462 10921 Msx2 msh homeobox 2 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:11744114 10921 Msx2 msh homeobox 2 gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141003 MGI PMID:11744114 10921 Msx2 msh homeobox 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20141003 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:15930102 10921 Msx2 msh homeobox 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12874124 10921 Msx2 msh homeobox 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20150205 MGI PMID:24715462 10921 Msx2 msh homeobox 2 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21693521 10921 Msx2 msh homeobox 2 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23090744 10921 Msx2 msh homeobox 2 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18442049 10921 Msx2 msh homeobox 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:18442049 10921 Msx2 msh homeobox 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20150205 MGI PMID:24715462 10921 Msx2 msh homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18442049 10921 Msx2 msh homeobox 2 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21693521 10921 Msx2 msh homeobox 2 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:12874124 10921 Msx2 msh homeobox 2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0003110 absent malleus processus brevis IAGP N RGD:5509061 20141003 MGI PMID:12701100 10921 Msx2 msh homeobox 2 gene MP:0003110 absent malleus processus brevis IAGP N RGD:5509061 20141003 MGI PMID:23090744 10921 Msx2 msh homeobox 2 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:12701100 10921 Msx2 msh homeobox 2 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21693521 10921 Msx2 msh homeobox 2 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:18442049 10921 Msx2 msh homeobox 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18442049 10921 Msx2 msh homeobox 2 gene MP:0004135 abnormal mammary gland embryonic development IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0004181 abnormal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21693521 10921 Msx2 msh homeobox 2 gene MP:0004343 small scapula IAGP N RGD:5509061 20141003 MGI PMID:15930102 10921 Msx2 msh homeobox 2 gene MP:0004378 frontal bone foramen IAGP N RGD:5509061 20141003 MGI PMID:14597577 10921 Msx2 msh homeobox 2 gene MP:0004378 frontal bone foramen IAGP N RGD:5509061 20171207 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0004444 small supraoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15930102 10921 Msx2 msh homeobox 2 gene MP:0004575 small limb buds IAGP N RGD:5509061 20141003 MGI PMID:15930102 10921 Msx2 msh homeobox 2 gene MP:0004691 absent pubis IAGP N RGD:5509061 20141003 MGI PMID:15930102 10921 Msx2 msh homeobox 2 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15930102 10921 Msx2 msh homeobox 2 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12701100 10921 Msx2 msh homeobox 2 gene MP:0005114 premature hair loss IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12701100 10921 Msx2 msh homeobox 2 gene MP:0006033 abnormal external auditory canal morphology IAGP N RGD:5509061 20141003 MGI PMID:12701100 10921 Msx2 msh homeobox 2 gene MP:0006200 vitreous body deposition IAGP N RGD:5509061 20141003 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:18442049 10921 Msx2 msh homeobox 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0008372 small malleus IAGP N RGD:5509061 20141003 MGI PMID:12701100 10921 Msx2 msh homeobox 2 gene MP:0008377 absent malleus manubrium IAGP N RGD:5509061 20141003 MGI PMID:12701100 10921 Msx2 msh homeobox 2 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20150903 MGI PMID:18667074 10921 Msx2 msh homeobox 2 gene MP:0008861 abnormal hair shedding IEA N RGD:5509061 20141003 MGI 10921 Msx2 msh homeobox 2 gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:23090744 10921 Msx2 msh homeobox 2 gene MP:0009742 increased cornea stroma thickness IAGP N RGD:5509061 20160310 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:23090744 10921 Msx2 msh homeobox 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20150903 MGI PMID:18667074 10921 Msx2 msh homeobox 2 gene MP:0010478 intracranial aneurysm IAGP N RGD:5509061 20141003 MGI PMID:21693521 10921 Msx2 msh homeobox 2 gene MP:0010747 abnormal enamel organ morphology IAGP N RGD:5509061 20180118 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15930102 10921 Msx2 msh homeobox 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18442049 10921 Msx2 msh homeobox 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12874124 10921 Msx2 msh homeobox 2 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141003 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0011513 abnormal vertebral artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21693521 10921 Msx2 msh homeobox 2 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20160310 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0012399 short nails IAGP N RGD:5509061 20141003 MGI PMID:21387539 10921 Msx2 msh homeobox 2 gene MP:0012401 long nails IAGP N RGD:5509061 20141003 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0012402 abnormal nail bed morphology IAGP N RGD:5509061 20141003 MGI PMID:21387539 10921 Msx2 msh homeobox 2 gene MP:0012403 abnormal nail plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21387539 10921 Msx2 msh homeobox 2 gene MP:0012405 abnormal nail matrix morphology IAGP N RGD:5509061 20141003 MGI PMID:21387539 10921 Msx2 msh homeobox 2 gene MP:0013765 iris hyperplasia IAGP N RGD:5509061 20150430 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:22503753 10921 Msx2 msh homeobox 2 gene MP:0030522 abnormal stellate reticulum morphology IAGP N RGD:5509061 20180118 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0030523 abnormal stratum intermedium morphology IAGP N RGD:5509061 20180118 MGI PMID:10742104 10921 Msx2 msh homeobox 2 gene MP:0030579 thoracoabdominoschisis IAGP N RGD:5509061 20180607 MGI PMID:18442049 10921 Msx2 msh homeobox 2 gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:23090744 10921 Msx2 msh homeobox 2 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20191128 MGI PMID:18667074 10927 Muc1 mucin 1, transmembrane gene MP:0000505 decreased digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:18719000 10927 Muc1 mucin 1, transmembrane gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17638868 10927 Muc1 mucin 1, transmembrane gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20377894 10927 Muc1 mucin 1, transmembrane gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:15075252 10927 Muc1 mucin 1, transmembrane gene MP:0002830 gallstones IAGP N RGD:5509061 20141003 MGI PMID:14703511 10927 Muc1 mucin 1, transmembrane gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:12618757 10927 Muc1 mucin 1, transmembrane gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:8530414 10927 Muc1 mucin 1, transmembrane gene MP:0005085 abnormal gallbladder physiology IAGP N RGD:5509061 20141003 MGI PMID:14703511 10927 Muc1 mucin 1, transmembrane gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:15075252 10927 Muc1 mucin 1, transmembrane gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17638868 10928 Muc2 mucin 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11872843 10928 Muc2 mucin 2 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11872843 10928 Muc2 mucin 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20150319 MGI PMID:24945909 10928 Muc2 mucin 2 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20150319 MGI PMID:24945909 10928 Muc2 mucin 2 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20150319 MGI PMID:24945909 10928 Muc2 mucin 2 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20111116 MGI 10928 Muc2 mucin 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0001666 abnormal intestinal absorption IEA N RGD:5509061 20111116 MGI 10928 Muc2 mucin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0002816 colitis IAGP N RGD:5509061 20150319 MGI PMID:24945909 10928 Muc2 mucin 2 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11872843 10928 Muc2 mucin 2 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:11872843 10928 Muc2 mucin 2 gene MP:0003292 melena IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20150319 MGI PMID:24945909 10928 Muc2 mucin 2 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11872843 10928 Muc2 mucin 2 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20150319 MGI PMID:24945909 10928 Muc2 mucin 2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0005036 diarrhea IEA N RGD:5509061 20111116 MGI 10928 Muc2 mucin 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11872843 10928 Muc2 mucin 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20150319 MGI PMID:11872843 10928 Muc2 mucin 2 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20150319 MGI PMID:24945909 10928 Muc2 mucin 2 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:18318598 10928 Muc2 mucin 2 gene MP:0014234 decreased enterocyte apoptosis IAGP N RGD:5509061 20230323 MGI PMID:11872843 10928 Muc2 mucin 2 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20161013 MGI PMID:18318598 10941 Mycl v-myc avian myelocytomatosis viral oncogene lung carcinoma derived gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8657155 10941 Mycl v-myc avian myelocytomatosis viral oncogene lung carcinoma derived gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24509714 10941 Mycl v-myc avian myelocytomatosis viral oncogene lung carcinoma derived gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:24509714 10941 Mycl v-myc avian myelocytomatosis viral oncogene lung carcinoma derived gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:24509714 10946 Myf6 myogenic factor 6 gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:10694423 10946 Myf6 myogenic factor 6 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:7588068 10946 Myf6 myogenic factor 6 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:7720708 10946 Myf6 myogenic factor 6 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:7797078 10946 Myf6 myogenic factor 6 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9268580 10946 Myf6 myogenic factor 6 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:7588068 10946 Myf6 myogenic factor 6 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:7797078 10946 Myf6 myogenic factor 6 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:9268580 10946 Myf6 myogenic factor 6 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:7588068 10946 Myf6 myogenic factor 6 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9268580 10946 Myf6 myogenic factor 6 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10694423 10946 Myf6 myogenic factor 6 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:18331721 10946 Myf6 myogenic factor 6 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:21212806 10946 Myf6 myogenic factor 6 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:10694423 10946 Myf6 myogenic factor 6 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:15386014 10946 Myf6 myogenic factor 6 gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10694423 10946 Myf6 myogenic factor 6 gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:7588068 10946 Myf6 myogenic factor 6 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:9268580 10946 Myf6 myogenic factor 6 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:17418413 10946 Myf6 myogenic factor 6 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17418413 10946 Myf6 myogenic factor 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:7720708 10946 Myf6 myogenic factor 6 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:7588068 10946 Myf6 myogenic factor 6 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9268580 10946 Myf6 myogenic factor 6 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15489287 10946 Myf6 myogenic factor 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17418413 10946 Myf6 myogenic factor 6 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:7720708 10946 Myf6 myogenic factor 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15489287 10946 Myf6 myogenic factor 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:7588068 10946 Myf6 myogenic factor 6 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:7797078 10946 Myf6 myogenic factor 6 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7588068 10946 Myf6 myogenic factor 6 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18331721 10946 Myf6 myogenic factor 6 gene MP:0003818 abnormal eye muscle development IAGP N RGD:5509061 20141003 MGI PMID:19531352 10946 Myf6 myogenic factor 6 gene MP:0003939 abnormal myotome morphology IAGP N RGD:5509061 20141003 MGI PMID:7588068 10946 Myf6 myogenic factor 6 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:10694423 10946 Myf6 myogenic factor 6 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:9268580 10946 Myf6 myogenic factor 6 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:7588068 10946 Myf6 myogenic factor 6 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:7720708 10946 Myf6 myogenic factor 6 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:8626014 10946 Myf6 myogenic factor 6 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:9268580 10946 Myf6 myogenic factor 6 gene MP:0004677 truncated ribs IAGP N RGD:5509061 20141003 MGI PMID:7588068 10946 Myf6 myogenic factor 6 gene MP:0004846 absent skeletal muscle IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0005247 abnormal extraocular muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19531352 10946 Myf6 myogenic factor 6 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:7588068 10946 Myf6 myogenic factor 6 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:7720708 10946 Myf6 myogenic factor 6 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9268580 10946 Myf6 myogenic factor 6 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:7588068 10946 Myf6 myogenic factor 6 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:7720708 10946 Myf6 myogenic factor 6 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21212806 10946 Myf6 myogenic factor 6 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:17418413 10946 Myf6 myogenic factor 6 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17418413 10946 Myf6 myogenic factor 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10694423 10946 Myf6 myogenic factor 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18331721 10946 Myf6 myogenic factor 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7588068 10946 Myf6 myogenic factor 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7720708 10946 Myf6 myogenic factor 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9609818 10946 Myf6 myogenic factor 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8626014 10946 Myf6 myogenic factor 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9268580 10946 Myf6 myogenic factor 6 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9268580 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10854329 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:10854329 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:19011095 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:19011095 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:10854329 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:10854329 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:19011095 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11715025 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0000741 impaired contractility of urinary bladder detrusor smooth muscle IAGP N RGD:5509061 20141003 MGI PMID:10854329 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19011095 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19011095 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0002328 abnormal airway resistance IAGP N RGD:5509061 20141003 MGI PMID:12959948 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:10854329 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:10854329 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:22511748 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:10854329 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:10854329 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:22511748 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0003622 ischuria IAGP N RGD:5509061 20141003 MGI PMID:19011095 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0003624 anuria IAGP N RGD:5509061 20141003 MGI PMID:10854329 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:10854329 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:19011095 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10854329 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:22511748 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:22511748 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19011095 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:10854329 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19011095 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21041690 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19011095 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10854329 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0012125 decreased bronchoconstrictive response IAGP N RGD:5509061 20141003 MGI PMID:12959948 10947 Myh11 myosin, heavy polypeptide 11, smooth muscle gene MP:0031510 increased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:22511748 10950 Myh3 myosin, heavy polypeptide 3, skeletal muscle, embryonic gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210513 MGI PMID:32094117 10950 Myh3 myosin, heavy polypeptide 3, skeletal muscle, embryonic gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20210513 MGI PMID:32094117 10950 Myh3 myosin, heavy polypeptide 3, skeletal muscle, embryonic gene MP:0009405 increased skeletal muscle fiber number IAGP N RGD:5509061 20210513 MGI PMID:32094117 10950 Myh3 myosin, heavy polypeptide 3, skeletal muscle, embryonic gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20210513 MGI PMID:32094117 10950 Myh3 myosin, heavy polypeptide 3, skeletal muscle, embryonic gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20210513 MGI PMID:32094117 10950 Myh3 myosin, heavy polypeptide 3, skeletal muscle, embryonic gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20210513 MGI PMID:32094117 10950 Myh3 myosin, heavy polypeptide 3, skeletal muscle, embryonic gene MP:0012185 abnormal muscle precursor cell morphology IAGP N RGD:5509061 20210513 MGI PMID:32094117 10950 Myh3 myosin, heavy polypeptide 3, skeletal muscle, embryonic gene MP:0030972 increased myoblast apoptosis IAGP N RGD:5509061 20210513 MGI PMID:32094117 10959 Myo1e myosin IE gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:17143286 10959 Myo1e myosin IE gene MP:0000315 hemoglobinuria IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0000767 abnormal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 10959 Myo1e myosin IE gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17143286 10959 Myo1e myosin IE gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 10959 Myo1e myosin IE gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17143286 10959 Myo1e myosin IE gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:17143286 10959 Myo1e myosin IE gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:17143286 10959 Myo1e myosin IE gene MP:0002847 abnormal renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:22811491 10959 Myo1e myosin IE gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:17143286 10959 Myo1e myosin IE gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17143286 10959 Myo1e myosin IE gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:17143286 10959 Myo1e myosin IE gene MP:0005161 hematuria IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:22811491 10959 Myo1e myosin IE gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 10959 Myo1e myosin IE gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17143286 10959 Myo1e myosin IE gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:22811491 10959 Myo1e myosin IE gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:22811491 10959 Myo1e myosin IE gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17143286 10959 Myo1e myosin IE gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:22811491 10959 Myo1e myosin IE gene MP:0011352 proximal convoluted tubule brush border loss IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:22811491 10959 Myo1e myosin IE gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:22811491 10959 Myo1e myosin IE gene MP:0011418 leukocyturia IAGP N RGD:5509061 20141003 MGI PMID:19005011 10959 Myo1e myosin IE gene MP:0011868 podocyte microvillus transformation IAGP N RGD:5509061 20141003 MGI PMID:22811491 10960 Myo1c myosin IC gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23593477 10960 Myo1c myosin IC gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23593477 10960 Myo1c myosin IC gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:23593477 10960 Myo1c myosin IC gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23593477 10960 Myo1c myosin IC gene MP:0004438 abnormal vestibular hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16102537 10960 Myo1c myosin IC gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:23593477 10960 Myo1c myosin IC gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:23593477 10961 Myo9b myosin IXb gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20566876 10961 Myo9b myosin IXb gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20566876 10961 Myo9b myosin IXb gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20566876 10961 Myo9b myosin IXb gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20566876 10962 Myo5b myosin VB gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20160407 MGI PMID:26201991 10962 Myo5b myosin VB gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20160407 MGI PMID:26201991 10962 Myo5b myosin VB gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20160922 MGI PMID:26392529 10962 Myo5b myosin VB gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20160407 MGI PMID:26201991 10962 Myo5b myosin VB gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20160922 MGI PMID:26392529 10962 Myo5b myosin VB gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20160407 MGI PMID:26201991 10962 Myo5b myosin VB gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160407 MGI PMID:26201991 10962 Myo5b myosin VB gene MP:0001263 weight loss IAGP N RGD:5509061 20160922 MGI PMID:26392529 10962 Myo5b myosin VB gene MP:0001429 dehydration IAGP N RGD:5509061 20160922 MGI PMID:26392529 10962 Myo5b myosin VB gene MP:0005036 diarrhea IAGP N RGD:5509061 20160407 MGI PMID:26201991 10962 Myo5b myosin VB gene MP:0005036 diarrhea IAGP N RGD:5509061 20160922 MGI PMID:26392529 10962 Myo5b myosin VB gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20160922 MGI PMID:26392529 10962 Myo5b myosin VB gene MP:0008109 abnormal small intestinal microvillus morphology IAGP N RGD:5509061 20160407 MGI PMID:26201991 10962 Myo5b myosin VB gene MP:0008109 abnormal small intestinal microvillus morphology IAGP N RGD:5509061 20160922 MGI PMID:26392529 10962 Myo5b myosin VB gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20160407 MGI PMID:26201991 10962 Myo5b myosin VB gene MP:0014078 small intestinal villus atrophy IAGP N RGD:5509061 20160922 MGI PMID:26392529 10962 Myo5b myosin VB gene MP:0014080 fused small intestinal villi IAGP N RGD:5509061 20160922 MGI PMID:26392529 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20231207 MGI 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20220714 MGI PMID:18812566 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0000736 delayed muscle development IAGP N RGD:5509061 20220714 MGI PMID:18812566 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0000745 tremors IEA N RGD:5509061 20230601 MGI 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0001116 small gonad IAGP N RGD:5509061 20220714 MGI PMID:35075134 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220714 MGI PMID:18812566 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0001406 abnormal gait IEA N RGD:5509061 20230601 MGI 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20220714 MGI PMID:18812566 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220714 MGI PMID:18812566 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18931680 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20159449 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20220714 MGI PMID:35075134 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0002058 neonatal lethality IEA N RGD:5509061 20111116 MGI 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0002210 abnormal sex determination IAGP N RGD:5509061 20220714 MGI PMID:35075134 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:18931680 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20159449 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20220714 MGI PMID:35075134 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20220714 MGI PMID:35075134 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20220714 MGI PMID:35075134 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20220714 MGI PMID:18812566 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20159449 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20220714 MGI PMID:35075134 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0004445 small exoccipital bone IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0004447 small basioccipital bone IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0004540 small maxilla IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0004592 small mandible IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20159449 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:20159449 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20221215 MGI 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20210520 MGI 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18931680 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18931680 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18931680 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20181227 MGI 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210128 MGI 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0005652 sex reversal IAGP N RGD:5509061 20220714 MGI PMID:35075134 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:20159449 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18931680 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18931680 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:20159449 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18931680 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:18931680 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:18931680 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:20159449 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:18931680 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20220714 MGI PMID:18812566 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20220714 MGI PMID:18812566 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20220714 MGI PMID:18812566 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20159449 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20220714 MGI PMID:18812566 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18931680 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20159449 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20220714 MGI PMID:18812566 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18562292 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20220714 MGI PMID:35075134 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20220714 MGI PMID:18812566 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20159449 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20220714 MGI PMID:18812566 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:20159449 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20220714 MGI PMID:18812566 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0012745 abnormal neural crest cell physiology IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0012755 decreased cranial neural crest cell number IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0012761 increased cranial neural crest cell apoptosis IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0030049 prominent forehead IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0030320 abnormal temporal bone tympanic part morphology IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:24080509 10967 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 gene MP:0031458 absent palate bones IAGP N RGD:5509061 20221124 MGI PMID:24080509 10969 Nefh neurofilament, heavy polypeptide gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:10402469 10969 Nefh neurofilament, heavy polypeptide gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9763429 10969 Nefh neurofilament, heavy polypeptide gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:10461886 10969 Nefh neurofilament, heavy polypeptide gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9763429 10969 Nefh neurofilament, heavy polypeptide gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10461886 10969 Nefh neurofilament, heavy polypeptide gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 10969 Nefh neurofilament, heavy polypeptide gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:9763429 10969 Nefh neurofilament, heavy polypeptide gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:10461886 10969 Nefh neurofilament, heavy polypeptide gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:17005864 10969 Nefh neurofilament, heavy polypeptide gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:14662745 10969 Nefh neurofilament, heavy polypeptide gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:10402469 10969 Nefh neurofilament, heavy polypeptide gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:10461886 10969 Nefh neurofilament, heavy polypeptide gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:12186852 10969 Nefh neurofilament, heavy polypeptide gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:14662745 10969 Nefh neurofilament, heavy polypeptide gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:9763431 10969 Nefh neurofilament, heavy polypeptide gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:10402469 10969 Nefh neurofilament, heavy polypeptide gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210520 MGI 10969 Nefh neurofilament, heavy polypeptide gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:14662745 10970 Nefm neurofilament, medium polypeptide gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:10402469 10970 Nefm neurofilament, medium polypeptide gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:22553027 10970 Nefm neurofilament, medium polypeptide gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10461886 10970 Nefm neurofilament, medium polypeptide gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:10461886 10970 Nefm neurofilament, medium polypeptide gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10461886 10970 Nefm neurofilament, medium polypeptide gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:22553027 10970 Nefm neurofilament, medium polypeptide gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:10461886 10970 Nefm neurofilament, medium polypeptide gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:17005864 10970 Nefm neurofilament, medium polypeptide gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:14662745 10970 Nefm neurofilament, medium polypeptide gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:10402469 10970 Nefm neurofilament, medium polypeptide gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:10461886 10970 Nefm neurofilament, medium polypeptide gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:14662745 10970 Nefm neurofilament, medium polypeptide gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:14662746 10970 Nefm neurofilament, medium polypeptide gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19193875 10970 Nefm neurofilament, medium polypeptide gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:9566972 10970 Nefm neurofilament, medium polypeptide gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:10402469 10970 Nefm neurofilament, medium polypeptide gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:14662745 10970 Nefm neurofilament, medium polypeptide gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:14662746 10970 Nefm neurofilament, medium polypeptide gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:22553027 10971 Nes nestin gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:21832185 10971 Nes nestin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21832185 10971 Nes nestin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20963821 10971 Nes nestin gene MP:0002833 increased heart weight IEA N RGD:5509061 20240523 MGI 10971 Nes nestin gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 10971 Nes nestin gene MP:0003631 nervous system phenotype IAGP N RGD:5509061 20230406 MGI PMID:34739481 10971 Nes nestin gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:20963821 10971 Nes nestin gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 10971 Nes nestin gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20230406 MGI PMID:34739481 10971 Nes nestin gene MP:0005380 embryo phenotype IAGP N RGD:5509061 20230406 MGI PMID:34739481 10971 Nes nestin gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:20963821 10971 Nes nestin gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:20963821 10971 Nes nestin gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20963821 10971 Nes nestin gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20963821 10971 Nes nestin gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20963821 10972 Neu1 neuraminidase 1 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19217813 10972 Neu1 neuraminidase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0003201 extremity edema IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0003622 ischuria IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19217813 10972 Neu1 neuraminidase 1 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0005060 accumulation of giant lysosomes in kidney/renal tubule cells IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:19217813 10972 Neu1 neuraminidase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:9363440 10972 Neu1 neuraminidase 1 gene MP:0006167 eyelid edema IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12023988 10972 Neu1 neuraminidase 1 gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19217813 10972 Neu1 neuraminidase 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12023988 10973 Nf1 neurofibromin 1 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:22868293 10973 Nf1 neurofibromin 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22868293 10973 Nf1 neurofibromin 1 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20600672 10973 Nf1 neurofibromin 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:22868293 10973 Nf1 neurofibromin 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20233966 10973 Nf1 neurofibromin 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:22118770 10973 Nf1 neurofibromin 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11297510 10973 Nf1 neurofibromin 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:7920653 10973 Nf1 neurofibromin 1 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:7920653 10973 Nf1 neurofibromin 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22118770 10973 Nf1 neurofibromin 1 gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:21478499 10973 Nf1 neurofibromin 1 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20151001 MGI PMID:12533510 10973 Nf1 neurofibromin 1 gene MP:0000597 delayed hepatic development IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:18614544 10973 Nf1 neurofibromin 1 gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:16906226 10973 Nf1 neurofibromin 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16906226 10973 Nf1 neurofibromin 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20160915 MGI PMID:23412344 10973 Nf1 neurofibromin 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:21478499 10973 Nf1 neurofibromin 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:21478499 10973 Nf1 neurofibromin 1 gene MP:0000736 delayed muscle development IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:10973261 10973 Nf1 neurofibromin 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20190207 MGI PMID:27482814 10973 Nf1 neurofibromin 1 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20151001 MGI PMID:12533510 10973 Nf1 neurofibromin 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11297510 10973 Nf1 neurofibromin 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:18371380 10973 Nf1 neurofibromin 1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0000863 abnormal secondary somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18371380 10973 Nf1 neurofibromin 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:18371380 10973 Nf1 neurofibromin 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:20600672 10973 Nf1 neurofibromin 1 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18371380 10973 Nf1 neurofibromin 1 gene MP:0000959 abnormal somatic sensory system morphology IAGP N RGD:5509061 20141003 MGI PMID:16906226 10973 Nf1 neurofibromin 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16906226 10973 Nf1 neurofibromin 1 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16906226 10973 Nf1 neurofibromin 1 gene MP:0001009 paravertebral ganglia hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0001010 prevertebral ganglia hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20190207 MGI PMID:27482814 10973 Nf1 neurofibromin 1 gene MP:0001148 enlarged testis IAGP N RGD:5509061 20190404 MGI PMID:30571760 10973 Nf1 neurofibromin 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20190404 MGI PMID:30571760 10973 Nf1 neurofibromin 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20190404 MGI PMID:30571760 10973 Nf1 neurofibromin 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20190207 MGI PMID:27482814 10973 Nf1 neurofibromin 1 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 10973 Nf1 neurofibromin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11297510 10973 Nf1 neurofibromin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18371380 10973 Nf1 neurofibromin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18614544 10973 Nf1 neurofibromin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21478499 10973 Nf1 neurofibromin 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20190207 MGI PMID:27482814 10973 Nf1 neurofibromin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0001267 enlarged chest IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160915 MGI PMID:23412344 10973 Nf1 neurofibromin 1 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20160915 MGI PMID:23412344 10973 Nf1 neurofibromin 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11297510 10973 Nf1 neurofibromin 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20600672 10973 Nf1 neurofibromin 1 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:21896734 10973 Nf1 neurofibromin 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10973261 10973 Nf1 neurofibromin 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18451155 10973 Nf1 neurofibromin 1 gene MP:0001396 unidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:18451155 10973 Nf1 neurofibromin 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11279521 10973 Nf1 neurofibromin 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20190207 MGI PMID:27482814 10973 Nf1 neurofibromin 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11279521 10973 Nf1 neurofibromin 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:9054942 10973 Nf1 neurofibromin 1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18451155 10973 Nf1 neurofibromin 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0001577 anemia IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11297510 10973 Nf1 neurofibromin 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18371380 10973 Nf1 neurofibromin 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18614544 10973 Nf1 neurofibromin 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:11297510 10973 Nf1 neurofibromin 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11297510 10973 Nf1 neurofibromin 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20190404 MGI PMID:30571760 10973 Nf1 neurofibromin 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20190404 MGI PMID:30571760 10973 Nf1 neurofibromin 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15652750 10973 Nf1 neurofibromin 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10591652 10973 Nf1 neurofibromin 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:7920653 10973 Nf1 neurofibromin 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 10973 Nf1 neurofibromin 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:18242513 10973 Nf1 neurofibromin 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:7920653 10973 Nf1 neurofibromin 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7920653 10973 Nf1 neurofibromin 1 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591652 10973 Nf1 neurofibromin 1 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 10973 Nf1 neurofibromin 1 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16397217 10973 Nf1 neurofibromin 1 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18242513 10973 Nf1 neurofibromin 1 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7920653 10973 Nf1 neurofibromin 1 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 10973 Nf1 neurofibromin 1 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20160929 MGI PMID:23858101 10973 Nf1 neurofibromin 1 gene MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:7920653 10973 Nf1 neurofibromin 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591652 10973 Nf1 neurofibromin 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 10973 Nf1 neurofibromin 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15652750 10973 Nf1 neurofibromin 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20160915 MGI PMID:23412344 10973 Nf1 neurofibromin 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20160929 MGI PMID:23858101 10973 Nf1 neurofibromin 1 gene MP:0002033 increased malignant triton tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 10973 Nf1 neurofibromin 1 gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 10973 Nf1 neurofibromin 1 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 10973 Nf1 neurofibromin 1 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20160929 MGI PMID:23858101 10973 Nf1 neurofibromin 1 gene MP:0002037 increased fibrohistocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 10973 Nf1 neurofibromin 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 10973 Nf1 neurofibromin 1 gene MP:0002039 increased neuroblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 10973 Nf1 neurofibromin 1 gene MP:0002039 increased neuroblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9214616 10973 Nf1 neurofibromin 1 gene MP:0002039 increased neuroblastoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 10973 Nf1 neurofibromin 1 gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7920653 10973 Nf1 neurofibromin 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15319471 10973 Nf1 neurofibromin 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15652750 10973 Nf1 neurofibromin 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16397217 10973 Nf1 neurofibromin 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:11297510 10973 Nf1 neurofibromin 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:18451155 10973 Nf1 neurofibromin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10591652 10973 Nf1 neurofibromin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10591653 10973 Nf1 neurofibromin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18242513 10973 Nf1 neurofibromin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18371380 10973 Nf1 neurofibromin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18451155 10973 Nf1 neurofibromin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19477430 10973 Nf1 neurofibromin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20233966 10973 Nf1 neurofibromin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21896734 10973 Nf1 neurofibromin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20160107 MGI PMID:25119042 10973 Nf1 neurofibromin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20160915 MGI PMID:23412344 10973 Nf1 neurofibromin 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21478499 10973 Nf1 neurofibromin 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10591652 10973 Nf1 neurofibromin 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21478499 10973 Nf1 neurofibromin 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10591652 10973 Nf1 neurofibromin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190207 MGI PMID:27482814 10973 Nf1 neurofibromin 1 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18371380 10973 Nf1 neurofibromin 1 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20600672 10973 Nf1 neurofibromin 1 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:7920653 10973 Nf1 neurofibromin 1 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 10973 Nf1 neurofibromin 1 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18768391 10973 Nf1 neurofibromin 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:15652750 10973 Nf1 neurofibromin 1 gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20190207 MGI PMID:27482814 10973 Nf1 neurofibromin 1 gene MP:0002802 abnormal discrimination learning IAGP N RGD:5509061 20141003 MGI PMID:11279521 10973 Nf1 neurofibromin 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20160107 MGI PMID:25119042 10973 Nf1 neurofibromin 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 10973 Nf1 neurofibromin 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20141003 MGI PMID:22868293 10973 Nf1 neurofibromin 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 10973 Nf1 neurofibromin 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:11297510 10973 Nf1 neurofibromin 1 gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20141003 MGI PMID:18371380 10973 Nf1 neurofibromin 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:15652750 10973 Nf1 neurofibromin 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18371380 10973 Nf1 neurofibromin 1 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 10973 Nf1 neurofibromin 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:7920653 10973 Nf1 neurofibromin 1 gene MP:0003808 increased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0003808 increased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141003 MGI PMID:18614544 10973 Nf1 neurofibromin 1 gene MP:0003834 abnormal adrenergic chromaffin cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:18614544 10973 Nf1 neurofibromin 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22118770 10973 Nf1 neurofibromin 1 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21478499 10973 Nf1 neurofibromin 1 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20190404 MGI PMID:30571760 10973 Nf1 neurofibromin 1 gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:21478499 10973 Nf1 neurofibromin 1 gene MP:0004309 absent otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0004573 absent limb buds IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:21478499 10973 Nf1 neurofibromin 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:18371380 10973 Nf1 neurofibromin 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:18371380 10973 Nf1 neurofibromin 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:22868293 10973 Nf1 neurofibromin 1 gene MP:0004987 abnormal osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:22868293 10973 Nf1 neurofibromin 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:18614544 10973 Nf1 neurofibromin 1 gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11297510 10973 Nf1 neurofibromin 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20190207 MGI PMID:27482814 10973 Nf1 neurofibromin 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20190207 MGI PMID:27482814 10973 Nf1 neurofibromin 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:16906226 10973 Nf1 neurofibromin 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7920653 10973 Nf1 neurofibromin 1 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:18614544 10973 Nf1 neurofibromin 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:20600672 10973 Nf1 neurofibromin 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20190404 MGI PMID:30571760 10973 Nf1 neurofibromin 1 gene MP:0005571 decreased lactate dehydrogenase level IEA N RGD:5509061 20160804 MGI 10973 Nf1 neurofibromin 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16906226 10973 Nf1 neurofibromin 1 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 10973 Nf1 neurofibromin 1 gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20141003 MGI PMID:18614544 10973 Nf1 neurofibromin 1 gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:18614544 10973 Nf1 neurofibromin 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22118770 10973 Nf1 neurofibromin 1 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:11297510 10973 Nf1 neurofibromin 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20190404 MGI PMID:30571760 10973 Nf1 neurofibromin 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:20600672 10973 Nf1 neurofibromin 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18371380 10973 Nf1 neurofibromin 1 gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22868293 10973 Nf1 neurofibromin 1 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0008301 adrenal medulla hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16906226 10973 Nf1 neurofibromin 1 gene MP:0008302 thin adrenal cortex IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141127 MGI PMID:18614544 10973 Nf1 neurofibromin 1 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:16906226 10973 Nf1 neurofibromin 1 gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:18768391 10973 Nf1 neurofibromin 1 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20190124 MGI PMID:25340873 10973 Nf1 neurofibromin 1 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20600672 10973 Nf1 neurofibromin 1 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21896734 10973 Nf1 neurofibromin 1 gene MP:0009233 enlarged sperm head IAGP N RGD:5509061 20190404 MGI PMID:30571760 10973 Nf1 neurofibromin 1 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10973261 10973 Nf1 neurofibromin 1 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15652750 10973 Nf1 neurofibromin 1 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18451155 10973 Nf1 neurofibromin 1 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 10973 Nf1 neurofibromin 1 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:21478499 10973 Nf1 neurofibromin 1 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21478499 10973 Nf1 neurofibromin 1 gene MP:0009460 skeletal muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0009770 abnormal optic chiasm morphology IAGP N RGD:5509061 20141003 MGI PMID:20600672 10973 Nf1 neurofibromin 1 gene MP:0009845 abnormal neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18242513 10973 Nf1 neurofibromin 1 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:21896734 10973 Nf1 neurofibromin 1 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141003 MGI PMID:20600672 10973 Nf1 neurofibromin 1 gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:18371380 10973 Nf1 neurofibromin 1 gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7920653 10973 Nf1 neurofibromin 1 gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10973261 10973 Nf1 neurofibromin 1 gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15319471 10973 Nf1 neurofibromin 1 gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18451155 10973 Nf1 neurofibromin 1 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:19477430 10973 Nf1 neurofibromin 1 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:20600672 10973 Nf1 neurofibromin 1 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:21896734 10973 Nf1 neurofibromin 1 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 10973 Nf1 neurofibromin 1 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:19477430 10973 Nf1 neurofibromin 1 gene MP:0010310 increased Schwannoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 10973 Nf1 neurofibromin 1 gene MP:0010314 increased neurofibroma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591652 10973 Nf1 neurofibromin 1 gene MP:0010314 increased neurofibroma incidence IAGP N RGD:5509061 20141003 MGI PMID:18242513 10973 Nf1 neurofibromin 1 gene MP:0010314 increased neurofibroma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 10973 Nf1 neurofibromin 1 gene MP:0010314 increased neurofibroma incidence IAGP N RGD:5509061 20190207 MGI PMID:27482814 10973 Nf1 neurofibromin 1 gene MP:0010334 pleural effusion IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0010361 increased gangliosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0010362 increased ganglioneuroma incidence IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7920653 10973 Nf1 neurofibromin 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12469121 10973 Nf1 neurofibromin 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0010614 abnormal mitral valve cusp morphology IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0010727 increased glioblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10973261 10973 Nf1 neurofibromin 1 gene MP:0010924 abnormal osteoid morphology IAGP N RGD:5509061 20141003 MGI PMID:22868293 10973 Nf1 neurofibromin 1 gene MP:0010929 increased osteoid thickness IAGP N RGD:5509061 20141003 MGI PMID:22868293 10973 Nf1 neurofibromin 1 gene MP:0010964 increased compact bone volume IAGP N RGD:5509061 20141003 MGI PMID:22868293 10973 Nf1 neurofibromin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10591652 10973 Nf1 neurofibromin 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10591653 10973 Nf1 neurofibromin 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18371380 10973 Nf1 neurofibromin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16906226 10973 Nf1 neurofibromin 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16906226 10973 Nf1 neurofibromin 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20151001 MGI PMID:12533510 10973 Nf1 neurofibromin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11297510 10973 Nf1 neurofibromin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16906226 10973 Nf1 neurofibromin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7920653 10973 Nf1 neurofibromin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190207 MGI PMID:27482814 10973 Nf1 neurofibromin 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10973 Nf1 neurofibromin 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16906226 10973 Nf1 neurofibromin 1 gene MP:0011180 abnormal hematopoietic cell number IAGP N RGD:5509061 20141003 MGI PMID:14982883 10973 Nf1 neurofibromin 1 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20151001 MGI PMID:12533510 10973 Nf1 neurofibromin 1 gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20151001 MGI PMID:12533510 10973 Nf1 neurofibromin 1 gene MP:0011364 abnormal metanephros morphology IAGP N RGD:5509061 20141003 MGI PMID:7926784 10973 Nf1 neurofibromin 1 gene MP:0011746 spleen fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16906226 10973 Nf1 neurofibromin 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20190404 MGI PMID:30571760 10973 Nf1 neurofibromin 1 gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21478499 10973 Nf1 neurofibromin 1 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:11297510 10973 Nf1 neurofibromin 1 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0012415 decreased sarcoma incidence IAGP N RGD:5509061 20160915 MGI PMID:23412344 10973 Nf1 neurofibromin 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 10973 Nf1 neurofibromin 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18242513 10973 Nf1 neurofibromin 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7920653 10973 Nf1 neurofibromin 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 10973 Nf1 neurofibromin 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160915 MGI PMID:23412344 10973 Nf1 neurofibromin 1 gene MP:0012761 increased cranial neural crest cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:7477259 10973 Nf1 neurofibromin 1 gene MP:0013693 abnormal hemopoiesis IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0014049 increased T cell acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20160818 MGI PMID:26764354 10973 Nf1 neurofibromin 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:10973261 10973 Nf1 neurofibromin 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:15652750 10973 Nf1 neurofibromin 1 gene MP:0020355 abnormal Sertoli cell barrier morphology IAGP N RGD:5509061 20190404 MGI PMID:30571760 10973 Nf1 neurofibromin 1 gene MP:0020549 increased optic chiasm size IAGP N RGD:5509061 20180301 MGI PMID:21896734 10973 Nf1 neurofibromin 1 gene MP:0030603 increased sperm number IAGP N RGD:5509061 20190404 MGI PMID:30571760 10973 Nf1 neurofibromin 1 gene MP:0030947 increased myoblast proliferation IAGP N RGD:5509061 20190725 MGI PMID:21478499 10973 Nf1 neurofibromin 1 gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:7926784 10974 Nfia nuclear factor I/A gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:17530927 10974 Nfia nuclear factor I/A gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:17530927 10974 Nfia nuclear factor I/A gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10518556 10974 Nfia nuclear factor I/A gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:12514217 10974 Nfia nuclear factor I/A gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:12514217 10974 Nfia nuclear factor I/A gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:10518556 10974 Nfia nuclear factor I/A gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:10518556 10974 Nfia nuclear factor I/A gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:17553984 10974 Nfia nuclear factor I/A gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:17553984 10974 Nfia nuclear factor I/A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10518556 10974 Nfia nuclear factor I/A gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:10518556 10974 Nfia nuclear factor I/A gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10518556 10974 Nfia nuclear factor I/A gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10518556 10974 Nfia nuclear factor I/A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17553984 10974 Nfia nuclear factor I/A gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17530927 10974 Nfia nuclear factor I/A gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:10518556 10974 Nfia nuclear factor I/A gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:17530927 10974 Nfia nuclear factor I/A gene MP:0003586 dilated ureter IAGP N RGD:5509061 20141003 MGI PMID:17530927 10974 Nfia nuclear factor I/A gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12514217 10974 Nfia nuclear factor I/A gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:12514217 10974 Nfia nuclear factor I/A gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:17530927 10974 Nfia nuclear factor I/A gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17530927 10974 Nfia nuclear factor I/A gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:10518556 10974 Nfia nuclear factor I/A gene MP:0004017 duplex kidney IAGP N RGD:5509061 20141003 MGI PMID:17530927 10974 Nfia nuclear factor I/A gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17553984 10974 Nfia nuclear factor I/A gene MP:0008221 abnormal hippocampal commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:12514217 10974 Nfia nuclear factor I/A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10518556 10974 Nfia nuclear factor I/A gene MP:0011488 abnormal ureterovesical junction morphology IAGP N RGD:5509061 20141003 MGI PMID:17530927 10974 Nfia nuclear factor I/A gene MP:0011493 double ureter IAGP N RGD:5509061 20141003 MGI PMID:17530927 10974 Nfia nuclear factor I/A gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20141003 MGI PMID:10518556 10974 Nfia nuclear factor I/A gene MP:0012545 syringomyelia IAGP N RGD:5509061 20141003 MGI PMID:17530927 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7590249 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:15845452 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:15845452 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:15845452 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:7590249 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:7590249 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:7590249 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:7590249 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7590249 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15845452 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14665694 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14665694 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9743524 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15845452 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0002869 increased anti-insulin autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:7590249 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:7590249 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:7590249 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14665694 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:7590249 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008180 abnormal marginal zone B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:14665694 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:14665694 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008638 increased circulating interleukin-1 alpha level IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14665694 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:20696914 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0010674 increased activation-induced B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0010836 decreased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21333553 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11067893 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15845452 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7590249 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8628301 10975 Nfkbia nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14665694 10978 Ngf nerve growth factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23091165 10978 Ngf nerve growth factor gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:19755105 10978 Ngf nerve growth factor gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:21151121 10978 Ngf nerve growth factor gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0001014 absent superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20200213 MGI PMID:31685654 10978 Ngf nerve growth factor gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:30612733 10978 Ngf nerve growth factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:30612733 10978 Ngf nerve growth factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20200213 MGI PMID:31685654 10978 Ngf nerve growth factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23091165 10978 Ngf nerve growth factor gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20200213 MGI PMID:31685654 10978 Ngf nerve growth factor gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20200213 MGI PMID:31685654 10978 Ngf nerve growth factor gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23091165 10978 Ngf nerve growth factor gene MP:0002083 premature death IAGP N RGD:5509061 20200213 MGI PMID:31685654 10978 Ngf nerve growth factor gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:30612733 10978 Ngf nerve growth factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23091165 10978 Ngf nerve growth factor gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20200213 MGI PMID:31685654 10978 Ngf nerve growth factor gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:23091165 10978 Ngf nerve growth factor gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:23091165 10978 Ngf nerve growth factor gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:23091165 10978 Ngf nerve growth factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:23091165 10978 Ngf nerve growth factor gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19755105 10978 Ngf nerve growth factor gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:23091165 10978 Ngf nerve growth factor gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23091165 10978 Ngf nerve growth factor gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23091165 10978 Ngf nerve growth factor gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23091165 10978 Ngf nerve growth factor gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20200310 MGI PMID:30612733 10978 Ngf nerve growth factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:23091165 10978 Ngf nerve growth factor gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23091165 10978 Ngf nerve growth factor gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23091165 10978 Ngf nerve growth factor gene MP:0006408 dorsal root ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20200213 MGI PMID:31685654 10978 Ngf nerve growth factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8137419 10978 Ngf nerve growth factor gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200213 MGI PMID:31685654 10978 Ngf nerve growth factor gene MP:0014488 abnormal skin sensory neuron innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:31685654 10978 Ngf nerve growth factor gene MP:0014488 abnormal skin sensory neuron innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:8137419 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:16564506 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20141003 MGI PMID:1317267 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0000578 ulcerated autopod IAGP N RGD:5509061 20141003 MGI PMID:1317267 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:10188952 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0000745 tremors IEA N RGD:5509061 20160421 MGI 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15126035 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:18786358 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:11745667 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10188952 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:10188952 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:1317267 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15126035 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:8128229 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:9268129 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001021 small L4 dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:10188952 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001022 abnormal L5 dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11559852 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10762318 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:15126035 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18772898 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:11559852 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10188952 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11559852 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17395831 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10188952 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11559852 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10188952 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11559852 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10762318 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:11559852 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:21413144 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11559852 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:17395831 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21413144 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11559852 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:1317267 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17395831 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:9268129 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10188952 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20160421 MGI 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21413144 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:11724766 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11559852 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:21413144 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:9268129 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:16564506 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17934455 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:18786358 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:23091165 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0003201 extremity edema IAGP N RGD:5509061 20141003 MGI PMID:1317267 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9472042 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10995552 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:15647357 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:18032673 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:18382462 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17395831 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17395831 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0003932 abnormal molar crown morphology IAGP N RGD:5509061 20141003 MGI PMID:9268129 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:11559852 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0004220 abnormal peripheral nervous system regeneration IAGP N RGD:5509061 20141003 MGI PMID:11745667 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10188952 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16564506 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:16564506 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:16564506 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16519950 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:12242267 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17493809 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:20133718 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:10188952 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0006070 increased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:12589782 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0006258 abnormal circumvallate papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:15126035 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0006260 abnormal gustatory papilla taste bud morphology IAGP N RGD:5509061 20141003 MGI PMID:15126035 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18786358 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17395831 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0008468 absent muscle spindles IAGP N RGD:5509061 20141003 MGI PMID:10188952 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0008486 decreased muscle spindle number IAGP N RGD:5509061 20141003 MGI PMID:10188952 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:20133718 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:17934455 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0008960 abnormal axon pruning IAGP N RGD:5509061 20141003 MGI PMID:18382462 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18032673 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10188952 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10188952 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11559852 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16564506 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0013818 abnormal oral cavity morphology IAGP N RGD:5509061 20230810 MGI PMID:9268129 10983 Ngfr nerve growth factor receptor (TNFR superfamily, member 16) gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 10985 Ninj1 ninjurin 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141009 MGI PMID:24347169 10985 Ninj1 ninjurin 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141009 MGI PMID:24347169 10985 Ninj1 ninjurin 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23690620 10985 Ninj1 ninjurin 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141009 MGI PMID:24347169 10985 Ninj1 ninjurin 1 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:23690620 10985 Ninj1 ninjurin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23690620 10985 Ninj1 ninjurin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23690620 10985 Ninj1 ninjurin 1 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141009 MGI PMID:24347169 10985 Ninj1 ninjurin 1 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141009 MGI PMID:24347169 10985 Ninj1 ninjurin 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141009 MGI PMID:24347169 10985 Ninj1 ninjurin 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141009 MGI PMID:24347169 10985 Ninj1 ninjurin 1 gene MP:0008007 abnormal cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:23690620 10987 Nmbr neuromedin B receptor gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:12231437 10987 Nmbr neuromedin B receptor gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9920658 10988 Nnt nicotinamide nucleotide transhydrogenase gene MP:0001406 abnormal gait IEA N RGD:5509061 20200514 MGI 10988 Nnt nicotinamide nucleotide transhydrogenase gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20161216 MGI PMID:22634753 10988 Nnt nicotinamide nucleotide transhydrogenase gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:16399503 10988 Nnt nicotinamide nucleotide transhydrogenase gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:16804088 10988 Nnt nicotinamide nucleotide transhydrogenase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16399503 10988 Nnt nicotinamide nucleotide transhydrogenase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16804088 10988 Nnt nicotinamide nucleotide transhydrogenase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16399503 10988 Nnt nicotinamide nucleotide transhydrogenase gene MP:0008291 abnormal adrenocortical cell morphology IAGP N RGD:5509061 20161216 MGI PMID:22634753 10988 Nnt nicotinamide nucleotide transhydrogenase gene MP:0014285 disorganized adrenal gland zona fasciculata IAGP N RGD:5509061 20230907 MGI PMID:22634753 10989 Nog noggin gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18096605 10989 Nog noggin gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:20063299 10989 Nog noggin gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:18096605 10989 Nog noggin gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11330864 10989 Nog noggin gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11330864 10989 Nog noggin gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11330864 10989 Nog noggin gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:21303853 10989 Nog noggin gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:21303853 10989 Nog noggin gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:21303853 10989 Nog noggin gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:21303853 10989 Nog noggin gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 10989 Nog noggin gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:17359964 10989 Nog noggin gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201022 MGI 10989 Nog noggin gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:17260385 10989 Nog noggin gene MP:0000537 abnormal urethra morphology IAGP N RGD:5509061 20141003 MGI PMID:18028901 10989 Nog noggin gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:11330864 10989 Nog noggin gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:9585504 10989 Nog noggin gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:17359964 10989 Nog noggin gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:21303853 10989 Nog noggin gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11330864 10989 Nog noggin gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:17260385 10989 Nog noggin gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:9585504 10989 Nog noggin gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11330864 10989 Nog noggin gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17260385 10989 Nog noggin gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21303853 10989 Nog noggin gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:9585504 10989 Nog noggin gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18028901 10989 Nog noggin gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:18028901 10989 Nog noggin gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12781691 10989 Nog noggin gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:12781691 10989 Nog noggin gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:9585504 10989 Nog noggin gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20210520 MGI 10989 Nog noggin gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:21303853 10989 Nog noggin gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:9585504 10989 Nog noggin gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20210520 MGI 10989 Nog noggin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9585504 10989 Nog noggin gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20210520 MGI 10989 Nog noggin gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 10989 Nog noggin gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20210520 MGI 10989 Nog noggin gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11330864 10989 Nog noggin gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:20508035 10989 Nog noggin gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:21303853 10989 Nog noggin gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9585504 10989 Nog noggin gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 10989 Nog noggin gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17260385 10989 Nog noggin gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17359964 10989 Nog noggin gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21303853 10989 Nog noggin gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9585504 10989 Nog noggin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:20508035 10989 Nog noggin gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:18028901 10989 Nog noggin gene MP:0002632 vestigial tail IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0002632 vestigial tail IAGP N RGD:5509061 20141003 MGI PMID:9585504 10989 Nog noggin gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20220811 MGI 10989 Nog noggin gene MP:0002770 absent bulbourethral gland IAGP N RGD:5509061 20141003 MGI PMID:18028901 10989 Nog noggin gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:17260385 10989 Nog noggin gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:9585504 10989 Nog noggin gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20210520 MGI 10989 Nog noggin gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 10989 Nog noggin gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 10989 Nog noggin gene MP:0003125 abnormal septation of the cloaca IAGP N RGD:5509061 20141003 MGI PMID:18028901 10989 Nog noggin gene MP:0003130 anal atresia IAGP N RGD:5509061 20141003 MGI PMID:18028901 10989 Nog noggin gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:20063299 10989 Nog noggin gene MP:0003160 abnormal esophagus development IAGP N RGD:5509061 20141003 MGI PMID:17260385 10989 Nog noggin gene MP:0003190 fused synovial joints IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20210520 MGI 10989 Nog noggin gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0003276 esophageal atresia IAGP N RGD:5509061 20141003 MGI PMID:17260385 10989 Nog noggin gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:17260385 10989 Nog noggin gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:21303853 10989 Nog noggin gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20230601 MGI 10989 Nog noggin gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:11330864 10989 Nog noggin gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:18028901 10989 Nog noggin gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:10559902 10989 Nog noggin gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:11330864 10989 Nog noggin gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0003740 fusion of middle ear ossicles IAGP N RGD:5509061 20141003 MGI PMID:18096605 10989 Nog noggin gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210128 MGI 10989 Nog noggin gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141003 MGI PMID:17359964 10989 Nog noggin gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20141003 MGI PMID:9585504 10989 Nog noggin gene MP:0003942 abnormal urinary system development IAGP N RGD:5509061 20141003 MGI PMID:18028901 10989 Nog noggin gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 10989 Nog noggin gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:18550712 10989 Nog noggin gene MP:0004387 abnormal prechordal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20508035 10989 Nog noggin gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:20063299 10989 Nog noggin gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:20063299 10989 Nog noggin gene MP:0004554 small pharynx IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0004575 small limb buds IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0004603 absent vertebral arch IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11134349 10989 Nog noggin gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20141003 MGI PMID:18096605 10989 Nog noggin gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18096605 10989 Nog noggin gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:18096605 10989 Nog noggin gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:18096605 10989 Nog noggin gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:20508035 10989 Nog noggin gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11330864 10989 Nog noggin gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0005315 absent pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:17359964 10989 Nog noggin gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:17359964 10989 Nog noggin gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20141003 MGI PMID:21303853 10989 Nog noggin gene MP:0006290 proboscis IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0006291 aprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0006293 absent nasal placodes IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0006295 absent sclerotome IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0006295 absent sclerotome IAGP N RGD:5509061 20141003 MGI PMID:21303853 10989 Nog noggin gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:18096605 10989 Nog noggin gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:18096605 10989 Nog noggin gene MP:0008320 absent adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:17359964 10989 Nog noggin gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:9585504 10989 Nog noggin gene MP:0008817 hematoma IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0008926 abnormal anterior definitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:20508035 10989 Nog noggin gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:20508035 10989 Nog noggin gene MP:0009570 abnormal right lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12781691 10989 Nog noggin gene MP:0009735 abnormal prostate gland development IAGP N RGD:5509061 20141003 MGI PMID:18028901 10989 Nog noggin gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11330864 10989 Nog noggin gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0010116 abnormal primitive urogenital sinus morphology IAGP N RGD:5509061 20141003 MGI PMID:18028901 10989 Nog noggin gene MP:0010884 esophagus stenosis IAGP N RGD:5509061 20150319 MGI PMID:17260385 10989 Nog noggin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11330864 10989 Nog noggin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16712836 10989 Nog noggin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9585504 10989 Nog noggin gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17260385 10989 Nog noggin gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16598734 10989 Nog noggin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10989 Nog noggin gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0011361 pelvic kidney IAGP N RGD:5509061 20141003 MGI PMID:18028901 10989 Nog noggin gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:21303853 10989 Nog noggin gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:9585504 10989 Nog noggin gene MP:0011759 absent Rathke's pouch IAGP N RGD:5509061 20141003 MGI PMID:17359964 10989 Nog noggin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18096605 10989 Nog noggin gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:10688202 10989 Nog noggin gene MP:0012176 abnormal head development IAGP N RGD:5509061 20141003 MGI PMID:21303853 10989 Nog noggin gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:17359964 10989 Nog noggin gene MP:0013352 abnormal Rathke's pouch apoptosis IAGP N RGD:5509061 20141218 MGI PMID:17359964 10989 Nog noggin gene MP:0014198 absent pituitary infundibular stalk IAGP N RGD:5509061 20160526 MGI PMID:17359964 10989 Nog noggin gene MP:0030066 short face IAGP N RGD:5509061 20170921 MGI PMID:16712836 10989 Nog noggin gene MP:0031362 decreased prostate gland ventral lobe weight IAGP N RGD:5509061 20220303 MGI PMID:18028901 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18413498 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15297441 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18433298 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15297441 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18433298 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18413498 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18413498 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:18413498 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11920687 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16246868 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18206129 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18206129 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:9681470 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9852587 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:10727738 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22522563 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10652188 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12072412 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18852886 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:11158630 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:11235982 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:7477374 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001356 increased aggression towards female mice IAGP N RGD:5509061 20141003 MGI PMID:7477374 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15158692 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001377 abnormal mating frequency IAGP N RGD:5509061 20141003 MGI PMID:12072412 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001377 abnormal mating frequency IAGP N RGD:5509061 20141003 MGI PMID:7477374 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22522563 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20141003 MGI PMID:12351742 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:15158692 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15158692 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:8978606 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12738065 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:10077313 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:18433298 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:18433298 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15155789 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:18413498 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18413498 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:15155789 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:10982771 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:22522563 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:12072412 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001752 abnormal hypothalamus secretion IAGP N RGD:5509061 20141003 MGI PMID:12072412 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12562678 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:10456061 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12072412 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:22522563 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12072412 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:9679181 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22522563 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12788381 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18413498 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7505721 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:10677545 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11992469 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:15297441 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:18413498 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:16246868 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:7518615 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:10362674 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11907582 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12788381 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11709397 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11907582 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12788381 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:12072412 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16246868 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12072412 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:10652188 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18852886 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:18433298 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18413498 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:18433298 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003023 decreased coronary flow rate IAGP N RGD:5509061 20141003 MGI PMID:10652188 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003063 increased coping response IAGP N RGD:5509061 20141003 MGI PMID:15158692 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003285 gastric hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10982771 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003307 pyloric stenosis IAGP N RGD:5509061 20141003 MGI PMID:12072412 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003307 pyloric stenosis IAGP N RGD:5509061 20141003 MGI PMID:7505721 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20220804 MGI PMID:9848082 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003434 decreased susceptibility to induced choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:11920687 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:12351742 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:10362674 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12781920 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15381772 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:18852886 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:10479702 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:18433298 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003821 decreased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:12788381 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:15158692 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:10479702 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:10982771 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:12072412 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:7505721 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0003991 arteriosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18413498 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18413498 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004036 abnormal muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:10444441 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004036 abnormal muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:10677545 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:11907582 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:12081996 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:12788381 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004220 abnormal peripheral nervous system regeneration IAGP N RGD:5509061 20141003 MGI PMID:11992469 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:10652188 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004495 decreased synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:9692709 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004545 enlarged esophagus IAGP N RGD:5509061 20141003 MGI PMID:10982771 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12072412 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:12072412 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10966931 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:12397095 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:18413498 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:18413498 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:18433298 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:12738065 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11907582 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:15381772 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005167 abnormal blood-brain barrier function IAGP N RGD:5509061 20141003 MGI PMID:17446423 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:9679181 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:9679181 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22522563 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:11158630 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:10905473 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:22522563 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22522563 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:9679181 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005575 increased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:9679181 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005585 increased tidal volume IAGP N RGD:5509061 20141003 MGI PMID:9679181 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11907582 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12788381 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005600 increased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12081996 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12788381 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22522563 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:16246868 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:11062295 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:7522345 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:11062295 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11907582 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12788381 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:9852587 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17446423 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:8667023 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:15297441 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:12788381 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0008779 abnormal maternal behavior IAGP N RGD:5509061 20141003 MGI PMID:10479702 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15155789 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9679181 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0008962 abnormal carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:9679181 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0009008 delayed estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:22522563 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:15297441 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0009349 increased urine pH IAGP N RGD:5509061 20141003 MGI PMID:10966931 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0009357 abnormal seizure response to inducing agent IAGP N RGD:5509061 20141003 MGI PMID:12781920 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:12351742 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:12351742 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9679181 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0009854 impaired gastric peristalsis IAGP N RGD:5509061 20150702 MGI PMID:10982771 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:12886012 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010017 visceral vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22522563 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010106 abnormal circulating pyruvate kinase level IAGP N RGD:5509061 20141003 MGI PMID:9681470 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:10966931 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010108 abnormal renal water reabsorption IAGP N RGD:5509061 20141003 MGI PMID:10966931 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:15297441 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010154 abnormal gastroesophageal sphincter physiology IAGP N RGD:5509061 20141003 MGI PMID:10444441 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010154 abnormal gastroesophageal sphincter physiology IAGP N RGD:5509061 20141003 MGI PMID:11438492 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:18852886 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010654 slow Wallerian degeneration IAGP N RGD:5509061 20220120 MGI PMID:11992469 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010781 pyloric sphincter hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10982771 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010781 pyloric sphincter hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010781 pyloric sphincter hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:7505721 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010782 stomach smooth muscle circular layer hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:7505721 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010783 abnormal stomach wall morphology IAGP N RGD:5509061 20141003 MGI PMID:7505721 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:15297441 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12704728 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0011462 increased urine bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:10966931 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0011508 abnormal glomerular capillary thrombosis IAGP N RGD:5509061 20141003 MGI PMID:16024729 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0011749 perivascular fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18413498 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0011882 enlarged duodenum IAGP N RGD:5509061 20150702 MGI PMID:10982771 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:22522563 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20170921 MGI PMID:10966931 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0020333 enhanced leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:10362674 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0020844 abnormal pulmonary respiratory rate response IAGP N RGD:5509061 20181101 MGI PMID:9679181 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0031182 abnormal cerebral blood flow rate IAGP N RGD:5509061 20201231 MGI PMID:12623792 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0031330 delayed peripheral nervous system regeneration IAGP N RGD:5509061 20220120 MGI PMID:11992469 10991 Nos1 nitric oxide synthase 1, neuronal gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:9848082 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18413498 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18433298 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18433298 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18413498 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10919259 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18413498 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000199 abnormal circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:11369002 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15971084 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:18413498 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11920687 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11435211 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000505 decreased digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:18719000 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:15199408 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:11751989 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20150716 MGI PMID:18272675 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:12090918 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12810565 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:10975863 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15821017 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15894526 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:16876161 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12738065 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:18433298 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:18433298 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11369002 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:18413498 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18413498 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:12016261 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:12646421 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9886418 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15556608 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:9886418 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:9236188 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9236188 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12562678 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9886418 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:10919259 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12562678 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:7539113 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001881 abnormal mammary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:20345368 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:12810565 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12090918 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17206489 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11731407 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17206489 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:9364062 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:11379816 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10919259 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12879252 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18413498 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:15821017 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:18413498 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:10919259 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11504701 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12810565 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:15205363 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20150716 MGI PMID:18272675 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16027239 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:7538909 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:15199408 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10788454 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9236188 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:14617760 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002602 abnormal eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9886418 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:11254671 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:15520837 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20141003 MGI PMID:11379816 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:14747298 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002865 increased growth rate IAGP N RGD:5509061 20141003 MGI PMID:11590438 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11590438 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:12054156 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:18433298 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:16460714 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:9486966 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19443702 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18413498 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:18433298 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12016261 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20141003 MGI PMID:15894526 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:11406467 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:14747298 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003177 allodynia IAGP N RGD:5509061 20141003 MGI PMID:11379816 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003194 abnormal frequency of paradoxical sleep IAGP N RGD:5509061 20141003 MGI PMID:12738065 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20150716 MGI PMID:18272675 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:11379816 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:16908860 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:19096157 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:16908860 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:19096157 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20150716 MGI PMID:18272675 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15567150 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003434 decreased susceptibility to induced choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:11920687 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:11731407 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:17206489 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:15546953 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:17206489 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:12054156 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:18433298 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003823 increased left ventricle developed pressure IAGP N RGD:5509061 20141003 MGI PMID:11509452 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003930 abnormal tooth hard tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15777672 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:16631135 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003966 abnormal adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:16631135 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10975863 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003991 arteriosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18413498 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:15546953 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0003995 abnormal uterine artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12090918 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18413498 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:10484522 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19096157 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:12016261 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004220 abnormal peripheral nervous system regeneration IAGP N RGD:5509061 20141003 MGI PMID:11379816 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20150716 MGI PMID:18272675 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004389 abnormal respiratory bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:11504701 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:9989972 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20141003 MGI PMID:16917077 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:9510198 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12810565 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:14747298 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:18413498 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:18413498 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:10948185 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:12054156 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:15777672 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:18433298 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:15777672 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20220922 MGI PMID:15777672 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:12738065 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9886418 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:15777672 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:7539113 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005124 increased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:20345368 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12016261 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:19443702 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12810565 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11369002 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005183 abnormal circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:10377046 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11590438 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11435211 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15821017 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005316 abnormal response to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11379816 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:12682064 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11504701 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12016261 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:10975863 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:11369002 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15199408 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7539113 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005410 abnormal fertilization IAGP N RGD:5509061 20141003 MGI PMID:16087361 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:14617760 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:7539113 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:11369002 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:12682064 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005582 increased renin activity IAGP N RGD:5509061 20141003 MGI PMID:18413498 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005610 increased circulating antidiuretic hormone level IAGP N RGD:5509061 20141003 MGI PMID:15971084 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19443702 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15556608 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:9364062 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0006141 abnormal atrioventricular node conduction IAGP N RGD:5509061 20141003 MGI PMID:12016261 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11369002 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16055518 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:20345368 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0006308 enlarged seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:12810565 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008011 intestine polyps IAGP N RGD:5509061 20150611 MGI PMID:23741483 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:15199408 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:19096157 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20150716 MGI PMID:18272675 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008287 abnormal subiculum morphology IAGP N RGD:5509061 20141003 MGI PMID:19096157 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:15777672 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20150716 MGI PMID:18272675 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:19096157 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9886418 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:14665440 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:7539113 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9886418 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:7538909 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:7539113 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008775 abnormal heart ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:12016261 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:19096157 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:10377046 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0009349 increased urine pH IAGP N RGD:5509061 20141003 MGI PMID:10966931 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0009548 abnormal platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:10788454 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0009623 enlarged inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15199408 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11369002 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12682064 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9236188 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9236188 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:11254671 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12682064 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:11751989 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:12749913 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:17206489 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0010017 visceral vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:17206489 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:12016261 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0010755 abnormal heart right ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:10484454 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0010781 pyloric sphincter hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:15777672 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0010961 increased compact bone mass IAGP N RGD:5509061 20141003 MGI PMID:15777672 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12704728 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0011508 abnormal glomerular capillary thrombosis IAGP N RGD:5509061 20141003 MGI PMID:16024729 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0011564 decreased urine prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:10788454 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0011742 decreased urine nitrite level IAGP N RGD:5509061 20141003 MGI PMID:9236188 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0011749 perivascular fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18413498 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:11590438 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20211021 MGI 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0013717 hyperlactation IAGP N RGD:5509061 20150611 MGI PMID:20345368 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:15777672 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0020478 abnormal circadian sleep/wake cycle IAGP N RGD:5509061 20171012 MGI PMID:12738065 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0020537 decreased subiculum size IAGP N RGD:5509061 20180301 MGI PMID:18272675 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0020537 decreased subiculum size IAGP N RGD:5509061 20180301 MGI PMID:19096157 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220519 MGI 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0030013 enhanced central nervous system regeneration IAGP N RGD:5509061 20170713 MGI PMID:15520837 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0030603 increased sperm number IAGP N RGD:5509061 20180621 MGI PMID:12810565 10996 Nos2 nitric oxide synthase 2, inducible gene MP:0031330 delayed peripheral nervous system regeneration IAGP N RGD:5509061 20220120 MGI PMID:11379816 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18413498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16763060 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18433298 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:11141498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16763060 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18433298 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18413498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18413498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20211021 MGI 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12781920 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15350840 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9201025 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:10435012 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:10652188 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:11457755 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:15350840 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:18413498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:7545787 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:9468189 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:9201025 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220804 MGI PMID:11779605 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:11907582 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:15699263 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11920687 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15016731 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12176963 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15350840 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:12176963 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:15350840 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15821017 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:9843834 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:11141498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:9843834 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18206129 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18206129 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:18206129 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:15305857 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:10727738 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9607805 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:18663015 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:18663015 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:9607805 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:15016731 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:15016731 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15016731 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16971655 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18206129 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12588707 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15350840 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15821017 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8917564 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10964974 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001378 abnormal ejaculation IAGP N RGD:5509061 20141003 MGI PMID:10549894 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001379 abnormal penile erection IAGP N RGD:5509061 20141003 MGI PMID:11904450 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10964974 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10964974 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:8978606 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:18433298 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:16763060 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:18433298 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15821017 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:18413498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:11457755 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11457755 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18413498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22467476 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:11457755 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16971655 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15016731 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:10435012 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:9201025 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15350840 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15841206 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:18663015 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12562678 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:10964974 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9607805 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:9607805 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10534440 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9607805 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15016731 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:15305857 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:10964974 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11457755 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11457755 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12788381 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15350840 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18413498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:9843834 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:10683374 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:15821017 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:18413498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17200185 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:10785232 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22467476 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12588707 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15016731 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11706934 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:10362674 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11907582 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12788381 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11907582 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12788381 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15350840 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:9201025 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:18206129 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:18663015 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18206129 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:11468208 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15350840 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:15350840 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10484454 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15350840 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:8917564 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:16971655 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15305857 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:11141498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:18433298 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18413498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:18433298 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0002989 small kidney IEA N RGD:5509061 20210128 MGI 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003023 decreased coronary flow rate IAGP N RGD:5509061 20141003 MGI PMID:10652188 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:10435012 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:10484454 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:9468189 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003033 abnormal pulmonary vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:9201025 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11141498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:16886062 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:11141498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11468208 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20141003 MGI PMID:15841206 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17200185 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:15016731 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:8917564 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:18663015 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20220804 MGI PMID:10377046 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17200185 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20141003 MGI PMID:9607805 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003547 abnormal pulmonary pressure IAGP N RGD:5509061 20141003 MGI PMID:10484454 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20141003 MGI PMID:9201025 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:10362674 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12781920 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:9201025 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003670 dilated renal glomerular capsule IAGP N RGD:5509061 20141003 MGI PMID:17200185 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:9607805 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:18433298 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003820 increased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:15841206 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003821 decreased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:12788381 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:16971655 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:10683374 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:22467476 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11907582 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:9692709 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0003991 arteriosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18413498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18413498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12588707 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15016731 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004044 aortic dissection IAGP N RGD:5509061 20141003 MGI PMID:11468208 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:11907582 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:12788381 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:9843834 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:16763060 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17200185 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:17200185 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15016731 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18256327 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:11907582 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17200185 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:10821808 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004857 abnormal heart weight IAGP N RGD:5509061 20141003 MGI PMID:15821017 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10362674 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11468208 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15821017 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22467476 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004877 abnormal systemic vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:9201025 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:18413498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:9502763 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:9616228 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:18413498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:15305857 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:18433298 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:11141498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:16763060 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20220811 MGI 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11468208 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11907582 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12176963 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15350840 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005167 abnormal blood-brain barrier function IAGP N RGD:5509061 20141003 MGI PMID:17446423 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:9607805 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11457755 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:10377046 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:9607805 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:10377046 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:11133872 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16971655 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17200185 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:10964974 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:10683374 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11141498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16971655 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17200185 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:22467476 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:10905473 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11457755 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:10435012 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:10652188 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:22467476 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:8917564 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:9468189 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:10683374 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:10683374 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11468208 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:16763060 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18206129 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:16971655 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:16886062 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:10683374 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16971655 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22467476 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18206129 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:10435012 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:11457755 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:7545787 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11907582 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12788381 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005600 increased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15841206 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12788381 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0006057 decreased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15350840 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10683374 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11907582 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12788381 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15350840 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15699263 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16971655 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22467476 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22081021 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22081021 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:8667023 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20151112 MGI 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:12176963 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:12788381 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20141003 MGI PMID:12176963 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0008823 abnormal interventricular septum membranous part morphology IAGP N RGD:5509061 20141003 MGI PMID:12176963 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:18663015 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15699263 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0008976 delayed female fertility IAGP N RGD:5509061 20141003 MGI PMID:10785232 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20220804 MGI PMID:10785232 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:10377046 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009007 short estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:10534440 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:10377046 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23291238 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009345 abnormal trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:11141498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009357 abnormal seizure response to inducing agent IAGP N RGD:5509061 20141003 MGI PMID:12781920 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:17200185 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11457755 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:18663015 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009648 abnormal superovulation IAGP N RGD:5509061 20220804 MGI PMID:10534440 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009648 abnormal superovulation IAGP N RGD:5509061 20220804 MGI PMID:10785232 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:11133872 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:11920687 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:18663015 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16886062 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11706934 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:15699263 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010017 visceral vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:12176963 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010180 increased susceptibility to weight loss IEA N RGD:5509061 20151112 MGI 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12176963 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010405 ostium secundum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:12176963 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12176963 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010483 aortic sinus aneurysm IAGP N RGD:5509061 20141003 MGI PMID:10683374 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20141003 MGI PMID:10821808 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010563 increased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:12176963 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:12176963 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:11468208 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010755 abnormal heart right ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:10484454 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010755 abnormal heart right ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:15821017 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010755 abnormal heart right ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010781 pyloric sphincter hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010814 absent alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:15016731 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0010894 pulmonary alveolar edema IAGP N RGD:5509061 20141003 MGI PMID:12176963 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12176963 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9843834 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15016731 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12704728 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011312 abnormal kidney afferent arteriole morphology IAGP N RGD:5509061 20141003 MGI PMID:16971655 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:16971655 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16971655 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011392 increased fetal cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12176963 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:16971655 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:16971655 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011508 abnormal glomerular capillary thrombosis IAGP N RGD:5509061 20141003 MGI PMID:16024729 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011508 abnormal glomerular capillary thrombosis IAGP N RGD:5509061 20141003 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011561 renal glomerulus lipidosis IAGP N RGD:5509061 20141003 MGI PMID:17200185 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0011749 perivascular fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18413498 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0012737 abnormal primary polar body morphology IAGP N RGD:5509061 20141003 MGI PMID:9607805 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231221 MGI PMID:15350840 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0014368 enhanced long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:10964974 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0020333 enhanced leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:10362674 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0021161 increased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:11468208 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0030984 increased circulating osteocalcin level IAGP N RGD:5509061 20201001 MGI PMID:16763060 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0031182 abnormal cerebral blood flow rate IAGP N RGD:5509061 20201231 MGI PMID:12781920 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0031274 increased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:11468208 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0031274 increased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:19036847 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:10785232 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:11779605 10997 Nos3 nitric oxide synthase 3, endothelial cell gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:9607805 10998 Notch1 notch 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:22484060 10998 Notch1 notch 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21562564 10998 Notch1 notch 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:17229764 10998 Notch1 notch 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:21305688 10998 Notch1 notch 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18227520 10998 Notch1 notch 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:10879540 10998 Notch1 notch 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:7789282 10998 Notch1 notch 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17336907 10998 Notch1 notch 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:23095891 10998 Notch1 notch 1 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:7789282 10998 Notch1 notch 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:17080428 10998 Notch1 notch 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15525534 10998 Notch1 notch 1 gene MP:0000387 disorganized inner root sheath cells IAGP N RGD:5509061 20141003 MGI PMID:15525534 10998 Notch1 notch 1 gene MP:0000388 absent hair follicle inner root sheath IAGP N RGD:5509061 20141003 MGI PMID:15525534 10998 Notch1 notch 1 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:15525534 10998 Notch1 notch 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:23293291 10998 Notch1 notch 1 gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:15525534 10998 Notch1 notch 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0000648 absent sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:15525534 10998 Notch1 notch 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:21562564 10998 Notch1 notch 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21562564 10998 Notch1 notch 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:10367900 10998 Notch1 notch 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:10367900 10998 Notch1 notch 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10367900 10998 Notch1 notch 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:18227520 10998 Notch1 notch 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10837027 10998 Notch1 notch 1 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 10998 Notch1 notch 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:15525534 10998 Notch1 notch 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:15525534 10998 Notch1 notch 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15525534 10998 Notch1 notch 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10367900 10998 Notch1 notch 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0001337 dry eyes IAGP N RGD:5509061 20141003 MGI PMID:23293291 10998 Notch1 notch 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 10998 Notch1 notch 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18227520 10998 Notch1 notch 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:18227520 10998 Notch1 notch 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17229764 10998 Notch1 notch 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15081359 10998 Notch1 notch 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:14595837 10998 Notch1 notch 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:10879540 10998 Notch1 notch 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:7789282 10998 Notch1 notch 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:10837027 10998 Notch1 notch 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18227520 10998 Notch1 notch 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21305688 10998 Notch1 notch 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7789282 10998 Notch1 notch 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10837027 10998 Notch1 notch 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12730124 10998 Notch1 notch 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:10837027 10998 Notch1 notch 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:10879540 10998 Notch1 notch 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:10837027 10998 Notch1 notch 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10879540 10998 Notch1 notch 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:7789282 10998 Notch1 notch 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10367900 10998 Notch1 notch 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10837027 10998 Notch1 notch 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18227520 10998 Notch1 notch 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8573724 10998 Notch1 notch 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:10837027 10998 Notch1 notch 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17658279 10998 Notch1 notch 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19110448 10998 Notch1 notch 1 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17261636 10998 Notch1 notch 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21311046 10998 Notch1 notch 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21562564 10998 Notch1 notch 1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:15525534 10998 Notch1 notch 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10367900 10998 Notch1 notch 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15525534 10998 Notch1 notch 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:14595837 10998 Notch1 notch 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:14595837 10998 Notch1 notch 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16885355 10998 Notch1 notch 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21562564 10998 Notch1 notch 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17261636 10998 Notch1 notch 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19110448 10998 Notch1 notch 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10367900 10998 Notch1 notch 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17261636 10998 Notch1 notch 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18227520 10998 Notch1 notch 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10367900 10998 Notch1 notch 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21991352 10998 Notch1 notch 1 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:17336907 10998 Notch1 notch 1 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 10998 Notch1 notch 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:10837027 10998 Notch1 notch 1 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20231109 MGI PMID:36325906 10998 Notch1 notch 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20160609 MGI PMID:26563570 10998 Notch1 notch 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20240530 MGI PMID:28395734 10998 Notch1 notch 1 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0003044 impaired basement membrane formation IAGP N RGD:5509061 20160609 MGI PMID:26563570 10998 Notch1 notch 1 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20240530 MGI PMID:28395734 10998 Notch1 notch 1 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:10837027 10998 Notch1 notch 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:10879540 10998 Notch1 notch 1 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:15525534 10998 Notch1 notch 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23806616 10998 Notch1 notch 1 gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20160609 MGI PMID:26563570 10998 Notch1 notch 1 gene MP:0003794 delayed somite formation IAGP N RGD:5509061 20141003 MGI PMID:7789282 10998 Notch1 notch 1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:15525534 10998 Notch1 notch 1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:21305688 10998 Notch1 notch 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:18635610 10998 Notch1 notch 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10879540 10998 Notch1 notch 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14595837 10998 Notch1 notch 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16885355 10998 Notch1 notch 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18227520 10998 Notch1 notch 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7926761 10998 Notch1 notch 1 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:21311046 10998 Notch1 notch 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0004125 abnormal venule morphology IAGP N RGD:5509061 20160609 MGI PMID:26563570 10998 Notch1 notch 1 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:18635610 10998 Notch1 notch 1 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:12730124 10998 Notch1 notch 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18227520 10998 Notch1 notch 1 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16163386 10998 Notch1 notch 1 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:16163386 10998 Notch1 notch 1 gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17080428 10998 Notch1 notch 1 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20240229 MGI PMID:37369584 10998 Notch1 notch 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16141228 10998 Notch1 notch 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20240229 MGI PMID:37369584 10998 Notch1 notch 1 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10837254 10998 Notch1 notch 1 gene MP:0004497 decreased organ of Corti supporting cell number IAGP N RGD:5509061 20141003 MGI PMID:16141228 10998 Notch1 notch 1 gene MP:0004712 notochord degeneration IAGP N RGD:5509061 20141003 MGI PMID:7789282 10998 Notch1 notch 1 gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:10837027 10998 Notch1 notch 1 gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:10837027 10998 Notch1 notch 1 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19110448 10998 Notch1 notch 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18227520 10998 Notch1 notch 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17658279 10998 Notch1 notch 1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:10367900 10998 Notch1 notch 1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:18227520 10998 Notch1 notch 1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:19110448 10998 Notch1 notch 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10367900 10998 Notch1 notch 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19110448 10998 Notch1 notch 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10879540 10998 Notch1 notch 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:7789282 10998 Notch1 notch 1 gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:7789282 10998 Notch1 notch 1 gene MP:0005224 abnormal left-right axis symmetry of the somites IAGP N RGD:5509061 20141003 MGI PMID:7789282 10998 Notch1 notch 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:21311046 10998 Notch1 notch 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17336907 10998 Notch1 notch 1 gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0005544 cornea deposits IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20160609 MGI PMID:26563570 10998 Notch1 notch 1 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10837027 10998 Notch1 notch 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20160609 MGI PMID:26563570 10998 Notch1 notch 1 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:21311046 10998 Notch1 notch 1 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:21305688 10998 Notch1 notch 1 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18227520 10998 Notch1 notch 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10367900 10998 Notch1 notch 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10367900 10998 Notch1 notch 1 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19110448 10998 Notch1 notch 1 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10367900 10998 Notch1 notch 1 gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19110448 10998 Notch1 notch 1 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18824585 10998 Notch1 notch 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:21562564 10998 Notch1 notch 1 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:17658279 10998 Notch1 notch 1 gene MP:0008758 abnormal T cell receptor beta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:19110448 10998 Notch1 notch 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:21991352 10998 Notch1 notch 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:17303760 10998 Notch1 notch 1 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:23095891 10998 Notch1 notch 1 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:10367900 10998 Notch1 notch 1 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18824585 10998 Notch1 notch 1 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:15081359 10998 Notch1 notch 1 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0008987 abnormal liver lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20141003 MGI PMID:15525534 10998 Notch1 notch 1 gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:18635610 10998 Notch1 notch 1 gene MP:0009165 abnormal endocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:18635610 10998 Notch1 notch 1 gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:18635610 10998 Notch1 notch 1 gene MP:0009328 delayed heart looping IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:20935640 10998 Notch1 notch 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20221215 MGI 10998 Notch1 notch 1 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20160609 MGI PMID:26563570 10998 Notch1 notch 1 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20231109 MGI PMID:36325906 10998 Notch1 notch 1 gene MP:0010500 myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21311046 10998 Notch1 notch 1 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21311046 10998 Notch1 notch 1 gene MP:0010561 absent coronary vessels IAGP N RGD:5509061 20141003 MGI PMID:21311046 10998 Notch1 notch 1 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20181122 MGI PMID:21493891 10998 Notch1 notch 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16163386 10998 Notch1 notch 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23806616 10998 Notch1 notch 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22156581 10998 Notch1 notch 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10879540 10998 Notch1 notch 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10367900 10998 Notch1 notch 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16885355 10998 Notch1 notch 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17215306 10998 Notch1 notch 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17229764 10998 Notch1 notch 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18227520 10998 Notch1 notch 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21305688 10998 Notch1 notch 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7789282 10998 Notch1 notch 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7926761 10998 Notch1 notch 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 10998 Notch1 notch 1 gene MP:0011181 increased hematopoietic cell number IAGP N RGD:5509061 20141003 MGI PMID:21562564 10998 Notch1 notch 1 gene MP:0011934 abnormal branching involved in pancreas development IAGP N RGD:5509061 20141003 MGI PMID:18635610 10998 Notch1 notch 1 gene MP:0011935 abnormal pancreatic bud formation IAGP N RGD:5509061 20141003 MGI PMID:18635610 10998 Notch1 notch 1 gene MP:0012246 abnormal hepatic cord morphology IAGP N RGD:5509061 20141003 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10837027 10998 Notch1 notch 1 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0012509 neural tube degeneration IAGP N RGD:5509061 20141003 MGI PMID:15809373 10998 Notch1 notch 1 gene MP:0012725 small sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:15525534 10998 Notch1 notch 1 gene MP:0013464 decreased conjunctiva goblet cell number IAGP N RGD:5509061 20150205 MGI PMID:23293291 10998 Notch1 notch 1 gene MP:0013925 abnormal vascular plexus formation IAGP N RGD:5509061 20160609 MGI PMID:26563570 10998 Notch1 notch 1 gene MP:0014148 lacrimal gland degeneration IAGP N RGD:5509061 20160407 MGI PMID:23293291 10998 Notch1 notch 1 gene MP:0014154 Meibomian gland degeneration IAGP N RGD:5509061 20160407 MGI PMID:23293291 10998 Notch1 notch 1 gene MP:0031124 aortic valve inflammation IAGP N RGD:5509061 20200917 MGI PMID:21493891 10998 Notch1 notch 1 gene MP:0031301 chronic liver inflammation IAGP N RGD:5509061 20211028 MGI PMID:21266774 10998 Notch1 notch 1 gene MP:0031518 calcified aortic valve cusp IAGP N RGD:5509061 20240118 MGI PMID:21493891 10999 Pnp purine-nucleoside phosphorylase gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9122228 10999 Pnp purine-nucleoside phosphorylase gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10859343 10999 Pnp purine-nucleoside phosphorylase gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9122228 10999 Pnp purine-nucleoside phosphorylase gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:10859343 10999 Pnp purine-nucleoside phosphorylase gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:9122228 10999 Pnp purine-nucleoside phosphorylase gene MP:0002494 increased IgM level IEA N RGD:5509061 20181011 MGI 10999 Pnp purine-nucleoside phosphorylase gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10859343 10999 Pnp purine-nucleoside phosphorylase gene MP:0005018 decreased T cell number IEA N RGD:5509061 20181011 MGI 10999 Pnp purine-nucleoside phosphorylase gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:10859343 10999 Pnp purine-nucleoside phosphorylase gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:10859343 10999 Pnp purine-nucleoside phosphorylase gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:1781357 10999 Pnp purine-nucleoside phosphorylase gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:9122228 10999 Pnp purine-nucleoside phosphorylase gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10859343 10999 Pnp purine-nucleoside phosphorylase gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9122228 10999 Pnp purine-nucleoside phosphorylase gene MP:0005093 decreased B cell proliferation IEA N RGD:5509061 20141003 MGI 10999 Pnp purine-nucleoside phosphorylase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:10859343 10999 Pnp purine-nucleoside phosphorylase gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:10859343 10999 Pnp purine-nucleoside phosphorylase gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:10859343 10999 Pnp purine-nucleoside phosphorylase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10859343 10999 Pnp purine-nucleoside phosphorylase gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10859343 10999 Pnp purine-nucleoside phosphorylase gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9122228 10999 Pnp purine-nucleoside phosphorylase gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10859343 10999 Pnp purine-nucleoside phosphorylase gene MP:0008168 decreased B-1a cell number IEA N RGD:5509061 20181011 MGI 10999 Pnp purine-nucleoside phosphorylase gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20181011 MGI 10999 Pnp purine-nucleoside phosphorylase gene MP:0008182 decreased marginal zone B cell number IEA N RGD:5509061 20141003 MGI 10999 Pnp purine-nucleoside phosphorylase gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20181011 MGI 10999 Pnp purine-nucleoside phosphorylase gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10859343 10999 Pnp purine-nucleoside phosphorylase gene MP:0010186 increased T follicular helper cell number IEA N RGD:5509061 20141003 MGI 10999 Pnp purine-nucleoside phosphorylase gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20181011 MGI 10999 Pnp purine-nucleoside phosphorylase gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 10999 Pnp purine-nucleoside phosphorylase gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 10999 Pnp purine-nucleoside phosphorylase gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 10999 Pnp purine-nucleoside phosphorylase gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 10999 Pnp purine-nucleoside phosphorylase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1781356 10999 Pnp purine-nucleoside phosphorylase gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1781356 10999 Pnp purine-nucleoside phosphorylase gene MP:0011476 abnormal urine nucleotide level IAGP N RGD:5509061 20141003 MGI PMID:2516826 10999 Pnp purine-nucleoside phosphorylase gene MP:0011477 abnormal urine nucleoside level IAGP N RGD:5509061 20141003 MGI PMID:10859343 10999 Pnp purine-nucleoside phosphorylase gene MP:0011597 decreased purine-nucleoside phosphorylase activity IAGP N RGD:5509061 20141003 MGI PMID:10859343 10999 Pnp purine-nucleoside phosphorylase gene MP:0011597 decreased purine-nucleoside phosphorylase activity IAGP N RGD:5509061 20141003 MGI PMID:1781357 10999 Pnp purine-nucleoside phosphorylase gene MP:0011597 decreased purine-nucleoside phosphorylase activity IAGP N RGD:5509061 20141003 MGI PMID:2516826 10999 Pnp purine-nucleoside phosphorylase gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 10999 Pnp purine-nucleoside phosphorylase gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20181011 MGI 11000 Npm1 nucleophosmin 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23226219 11000 Npm1 nucleophosmin 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23226219 11000 Npm1 nucleophosmin 1 gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20171109 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23226219 11000 Npm1 nucleophosmin 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20171109 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:23226219 11000 Npm1 nucleophosmin 1 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16199867 11000 Npm1 nucleophosmin 1 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20171109 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23226219 11000 Npm1 nucleophosmin 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16199867 11000 Npm1 nucleophosmin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16199867 11000 Npm1 nucleophosmin 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:16199867 11000 Npm1 nucleophosmin 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16199867 11000 Npm1 nucleophosmin 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:23226219 11000 Npm1 nucleophosmin 1 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20171109 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20171109 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20171109 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20171109 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0004049 increased acute promyelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21979879 11000 Npm1 nucleophosmin 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23226219 11000 Npm1 nucleophosmin 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20190418 MGI PMID:30692594 11000 Npm1 nucleophosmin 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23226219 11000 Npm1 nucleophosmin 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:23226219 11000 Npm1 nucleophosmin 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16199867 11000 Npm1 nucleophosmin 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23226219 11000 Npm1 nucleophosmin 1 gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:23226219 11000 Npm1 nucleophosmin 1 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:23226219 11000 Npm1 nucleophosmin 1 gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20171109 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20190418 MGI PMID:30692594 11000 Npm1 nucleophosmin 1 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23226219 11000 Npm1 nucleophosmin 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21979879 11000 Npm1 nucleophosmin 1 gene MP:0011087 neonatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 11000 Npm1 nucleophosmin 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21979879 11000 Npm1 nucleophosmin 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23226219 11000 Npm1 nucleophosmin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16199867 11000 Npm1 nucleophosmin 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20171109 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:16199867 11000 Npm1 nucleophosmin 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0011877 absent liver IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21441929 11000 Npm1 nucleophosmin 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16199867 11000 Npm1 nucleophosmin 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16007073 11000 Npm1 nucleophosmin 1 gene MP:0013660 abnormal bone marrow hematopoietic cell morphology IAGP N RGD:5509061 20190418 MGI PMID:30692594 11000 Npm1 nucleophosmin 1 gene MP:0013696 increased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20190418 MGI PMID:30692594 11003 Nppa natriuretic peptide type A gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20180719 MGI PMID:7839143 11003 Nppa natriuretic peptide type A gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20180719 MGI PMID:10848509 11003 Nppa natriuretic peptide type A gene MP:0000231 hypertension IAGP N RGD:5509061 20180719 MGI PMID:7839143 11003 Nppa natriuretic peptide type A gene MP:0000274 enlarged heart IAGP N RGD:5509061 20180719 MGI PMID:7839143 11003 Nppa natriuretic peptide type A gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20180719 MGI PMID:10330043 11003 Nppa natriuretic peptide type A gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20180719 MGI PMID:10956626 11003 Nppa natriuretic peptide type A gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20180719 MGI PMID:10100923 11003 Nppa natriuretic peptide type A gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20180719 MGI PMID:10330043 11003 Nppa natriuretic peptide type A gene MP:0002626 increased heart rate IAGP N RGD:5509061 20180719 MGI PMID:10484477 11003 Nppa natriuretic peptide type A gene MP:0002833 increased heart weight IAGP N RGD:5509061 20180719 MGI PMID:7839143 11003 Nppa natriuretic peptide type A gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20180719 MGI PMID:10100923 11003 Nppa natriuretic peptide type A gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20180719 MGI PMID:10330043 11003 Nppa natriuretic peptide type A gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20180719 MGI PMID:10484477 11003 Nppa natriuretic peptide type A gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20180719 MGI PMID:7839143 11003 Nppa natriuretic peptide type A gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20180719 MGI PMID:9458926 11003 Nppa natriuretic peptide type A gene MP:0005532 abnormal vascular resistance IAGP N RGD:5509061 20180719 MGI PMID:10100923 11003 Nppa natriuretic peptide type A gene MP:0005581 abnormal renin activity IAGP N RGD:5509061 20180719 MGI PMID:9458926 11003 Nppa natriuretic peptide type A gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20180719 MGI PMID:10330043 11003 Nppa natriuretic peptide type A gene MP:0005662 increased circulating adrenaline level IAGP N RGD:5509061 20180719 MGI PMID:10484477 11003 Nppa natriuretic peptide type A gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20180719 MGI PMID:10100923 11003 Nppa natriuretic peptide type A gene MP:0008776 increased right ventricle peak pressure IAGP N RGD:5509061 20180719 MGI PMID:10330043 11003 Nppa natriuretic peptide type A gene MP:0008776 increased right ventricle peak pressure IAGP N RGD:5509061 20180719 MGI PMID:10956626 11003 Nppa natriuretic peptide type A gene MP:0010109 abnormal renal sodium reabsorption IAGP N RGD:5509061 20180719 MGI PMID:9458926 11003 Nppa natriuretic peptide type A gene MP:0010755 abnormal heart right ventricle pressure IAGP N RGD:5509061 20180719 MGI PMID:10956626 11004 Nppb natriuretic peptide type B gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10737768 11004 Nppb natriuretic peptide type B gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10737768 11004 Nppb natriuretic peptide type B gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:10737768 11007 Npr1 natriuretic peptide receptor 1 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11997476 11007 Npr1 natriuretic peptide receptor 1 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9287305 11007 Npr1 natriuretic peptide receptor 1 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:12124219 11007 Npr1 natriuretic peptide receptor 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:12124219 11007 Npr1 natriuretic peptide receptor 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12727932 11007 Npr1 natriuretic peptide receptor 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160929 MGI PMID:25775533 11007 Npr1 natriuretic peptide receptor 1 gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:12727932 11007 Npr1 natriuretic peptide receptor 1 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:11997476 11007 Npr1 natriuretic peptide receptor 1 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:9287305 11007 Npr1 natriuretic peptide receptor 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12124219 11007 Npr1 natriuretic peptide receptor 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12727932 11007 Npr1 natriuretic peptide receptor 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15769452 11007 Npr1 natriuretic peptide receptor 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:23464624 11007 Npr1 natriuretic peptide receptor 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9405681 11007 Npr1 natriuretic peptide receptor 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20160929 MGI PMID:25775533 11007 Npr1 natriuretic peptide receptor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15769452 11007 Npr1 natriuretic peptide receptor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9405681 11007 Npr1 natriuretic peptide receptor 1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:7477288 11007 Npr1 natriuretic peptide receptor 1 gene MP:0002295 abnormal pulmonary circulation IAGP N RGD:5509061 20141003 MGI PMID:9405681 11007 Npr1 natriuretic peptide receptor 1 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:23464624 11007 Npr1 natriuretic peptide receptor 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:9405681 11007 Npr1 natriuretic peptide receptor 1 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:9405681 11007 Npr1 natriuretic peptide receptor 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:10537139 11007 Npr1 natriuretic peptide receptor 1 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:10537139 11007 Npr1 natriuretic peptide receptor 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:23464624 11007 Npr1 natriuretic peptide receptor 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7477288 11007 Npr1 natriuretic peptide receptor 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9482923 11007 Npr1 natriuretic peptide receptor 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20160929 MGI PMID:25775533 11007 Npr1 natriuretic peptide receptor 1 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9482923 11007 Npr1 natriuretic peptide receptor 1 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:11457873 11007 Npr1 natriuretic peptide receptor 1 gene MP:0003353 decreased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:9405681 11007 Npr1 natriuretic peptide receptor 1 gene MP:0004044 aortic dissection IAGP N RGD:5509061 20141003 MGI PMID:9405681 11007 Npr1 natriuretic peptide receptor 1 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:12727932 11007 Npr1 natriuretic peptide receptor 1 gene MP:0004216 salt-resistant hypertension IAGP N RGD:5509061 20141003 MGI PMID:7477288 11007 Npr1 natriuretic peptide receptor 1 gene MP:0004216 salt-resistant hypertension IAGP N RGD:5509061 20141003 MGI PMID:9405681 11007 Npr1 natriuretic peptide receptor 1 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23464624 11007 Npr1 natriuretic peptide receptor 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9405681 11007 Npr1 natriuretic peptide receptor 1 gene MP:0005522 increased circulating atrial natriuretic factor IAGP N RGD:5509061 20141003 MGI PMID:12124219 11007 Npr1 natriuretic peptide receptor 1 gene MP:0005522 increased circulating atrial natriuretic factor IAGP N RGD:5509061 20141003 MGI PMID:12727932 11007 Npr1 natriuretic peptide receptor 1 gene MP:0005522 increased circulating atrial natriuretic factor IAGP N RGD:5509061 20141003 MGI PMID:9287305 11007 Npr1 natriuretic peptide receptor 1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12727932 11007 Npr1 natriuretic peptide receptor 1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9405681 11007 Npr1 natriuretic peptide receptor 1 gene MP:0005647 abnormal sex gland physiology IAGP N RGD:5509061 20141003 MGI PMID:10537139 11007 Npr1 natriuretic peptide receptor 1 gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:9405681 11007 Npr1 natriuretic peptide receptor 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:12727932 11007 Npr1 natriuretic peptide receptor 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:15769452 11007 Npr1 natriuretic peptide receptor 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:9405681 11007 Npr1 natriuretic peptide receptor 1 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7477288 11007 Npr1 natriuretic peptide receptor 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23464624 11007 Npr1 natriuretic peptide receptor 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7477288 11007 Npr1 natriuretic peptide receptor 1 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12727932 11007 Npr1 natriuretic peptide receptor 1 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:11457873 11007 Npr1 natriuretic peptide receptor 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20160929 MGI PMID:25775533 11007 Npr1 natriuretic peptide receptor 1 gene MP:0031080 pulmonary embolism IAGP N RGD:5509061 20200709 MGI PMID:9405681 11008 Npr3 natriuretic peptide receptor 3 gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20190110 MGI PMID:27959934 11008 Npr3 natriuretic peptide receptor 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20150917 MGI PMID:23979929 11008 Npr3 natriuretic peptide receptor 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20190110 MGI PMID:27959934 11008 Npr3 natriuretic peptide receptor 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 11008 Npr3 natriuretic peptide receptor 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 11008 Npr3 natriuretic peptide receptor 3 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20150917 MGI PMID:23979929 11008 Npr3 natriuretic peptide receptor 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 11008 Npr3 natriuretic peptide receptor 3 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 11008 Npr3 natriuretic peptide receptor 3 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0001257 increased body length IAGP N RGD:5509061 20150917 MGI PMID:23979929 11008 Npr3 natriuretic peptide receptor 3 gene MP:0001257 increased body length IAGP N RGD:5509061 20190110 MGI PMID:27959934 11008 Npr3 natriuretic peptide receptor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 11008 Npr3 natriuretic peptide receptor 3 gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20111116 MGI 11008 Npr3 natriuretic peptide receptor 3 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20150917 MGI PMID:23979929 11008 Npr3 natriuretic peptide receptor 3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0002758 long tail IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20190110 MGI PMID:27959934 11008 Npr3 natriuretic peptide receptor 3 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20190110 MGI PMID:27959934 11008 Npr3 natriuretic peptide receptor 3 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20190110 MGI PMID:27959934 11008 Npr3 natriuretic peptide receptor 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20190110 MGI PMID:27959934 11008 Npr3 natriuretic peptide receptor 3 gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20150917 MGI PMID:23979929 11008 Npr3 natriuretic peptide receptor 3 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0004641 elongated metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0004651 increased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0004685 calcified intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0004695 increased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0004695 increased length of long bones IAGP N RGD:5509061 20190110 MGI PMID:27959934 11008 Npr3 natriuretic peptide receptor 3 gene MP:0004703 abnormal vertebral column morphology IEA N RGD:5509061 20111116 MGI 11008 Npr3 natriuretic peptide receptor 3 gene MP:0004705 elongated vertebral body IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0004705 elongated vertebral body IAGP N RGD:5509061 20190110 MGI PMID:27959934 11008 Npr3 natriuretic peptide receptor 3 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0006253 clinodactyly IEA N RGD:5509061 20111116 MGI 11008 Npr3 natriuretic peptide receptor 3 gene MP:0006296 arachnodactyly IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0006296 arachnodactyly IAGP N RGD:5509061 20150917 MGI PMID:23979929 11008 Npr3 natriuretic peptide receptor 3 gene MP:0006320 abnormal interscapular fat pad morphology IAGP N RGD:5509061 20180111 MGI PMID:22307324 11008 Npr3 natriuretic peptide receptor 3 gene MP:0006392 abnormal nucleus pulposus morphology IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0006393 absent nucleus pulposus IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0006394 abnormal vertebral epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10468599 11008 Npr3 natriuretic peptide receptor 3 gene MP:0006394 abnormal vertebral epiphyseal plate morphology IAGP N RGD:5509061 20190110 MGI PMID:27959934 11008 Npr3 natriuretic peptide receptor 3 gene MP:0008771 elongated vertebral column IEA N RGD:5509061 20111116 MGI 11008 Npr3 natriuretic peptide receptor 3 gene MP:0008833 caudal hemivertebra IAGP N RGD:5509061 20150917 MGI PMID:23979929 11008 Npr3 natriuretic peptide receptor 3 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20180111 MGI PMID:22307324 11008 Npr3 natriuretic peptide receptor 3 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20180111 MGI PMID:22307324 11008 Npr3 natriuretic peptide receptor 3 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20180111 MGI PMID:22307324 11008 Npr3 natriuretic peptide receptor 3 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20180111 MGI PMID:22307324 11008 Npr3 natriuretic peptide receptor 3 gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20180111 MGI PMID:22307324 11008 Npr3 natriuretic peptide receptor 3 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20180111 MGI PMID:22307324 11008 Npr3 natriuretic peptide receptor 3 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20190110 MGI PMID:27959934 11008 Npr3 natriuretic peptide receptor 3 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20190110 MGI PMID:27959934 11008 Npr3 natriuretic peptide receptor 3 gene MP:0010128 hypovolemia IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0011476 abnormal urine nucleotide level IAGP N RGD:5509061 20141003 MGI PMID:10377427 11008 Npr3 natriuretic peptide receptor 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20141003 MGI 11008 Npr3 natriuretic peptide receptor 3 gene MP:0013138 thin body IAGP N RGD:5509061 20150917 MGI PMID:23979929 11016 Npy neuropeptide Y gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:8632796 11016 Npy neuropeptide Y gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16339312 11016 Npy neuropeptide Y gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18616565 11016 Npy neuropeptide Y gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18616565 11016 Npy neuropeptide Y gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:18616565 11016 Npy neuropeptide Y gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20613867 11016 Npy neuropeptide Y gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12077332 11016 Npy neuropeptide Y gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160310 MGI PMID:26402609 11016 Npy neuropeptide Y gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:18616565 11016 Npy neuropeptide Y gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:16339312 11016 Npy neuropeptide Y gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:8632796 11016 Npy neuropeptide Y gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:20613867 11016 Npy neuropeptide Y gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20141003 MGI PMID:18616565 11016 Npy neuropeptide Y gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:20613867 11016 Npy neuropeptide Y gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:20613867 11016 Npy neuropeptide Y gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:20613867 11016 Npy neuropeptide Y gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16339312 11016 Npy neuropeptide Y gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20613867 11016 Npy neuropeptide Y gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:20613867 11016 Npy neuropeptide Y gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20160407 MGI PMID:20613867 11016 Npy neuropeptide Y gene MP:0014145 increased white adipose tissue mass IAGP N RGD:5509061 20160407 MGI PMID:20613867 11016 Npy neuropeptide Y gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20160407 MGI PMID:20613867 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20151119 MGI PMID:22768253 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:9623983 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0001260 increased body weight IAGP N RGD:5509061 20151119 MGI PMID:22768253 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:10698177 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:14525913 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:9623983 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20151119 MGI PMID:22768253 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20151119 MGI PMID:22768253 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:9623983 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230119 MGI 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:14525913 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14525913 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:9623983 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230119 MGI 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230119 MGI 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20151119 MGI PMID:22768253 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20151119 MGI PMID:22768253 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20151119 MGI PMID:22768253 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:16636293 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:14525913 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:9623983 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:14525913 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:9623983 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20151119 MGI PMID:22768253 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20151119 MGI PMID:22768253 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20151119 MGI PMID:22768253 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20151119 MGI PMID:22768253 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:10698177 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20151119 MGI PMID:22768253 11017 Npy5r neuropeptide Y receptor Y5 gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20151119 MGI PMID:22768253 11018 Nras neuroblastoma ras oncogene gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:22876308 11018 Nras neuroblastoma ras oncogene gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:23733505 11018 Nras neuroblastoma ras oncogene gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180719 MGI PMID:23733505 11018 Nras neuroblastoma ras oncogene gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:23733505 11018 Nras neuroblastoma ras oncogene gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:22876308 11018 Nras neuroblastoma ras oncogene gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0000292 distended pericardium IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20180719 MGI PMID:22876308 11018 Nras neuroblastoma ras oncogene gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20180719 MGI PMID:23303902 11018 Nras neuroblastoma ras oncogene gene MP:0000592 short tail IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0000601 small liver IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0000603 pale liver IAGP N RGD:5509061 20180719 MGI PMID:22876308 11018 Nras neuroblastoma ras oncogene gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180719 MGI PMID:21586752 11018 Nras neuroblastoma ras oncogene gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180719 MGI PMID:23733505 11018 Nras neuroblastoma ras oncogene gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20180719 MGI PMID:22876308 11018 Nras neuroblastoma ras oncogene gene MP:0000745 tremors IAGP N RGD:5509061 20180719 MGI PMID:23303902 11018 Nras neuroblastoma ras oncogene gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20180719 MGI PMID:23303902 11018 Nras neuroblastoma ras oncogene gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20180719 MGI PMID:25252692 11018 Nras neuroblastoma ras oncogene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180719 MGI PMID:22876308 11018 Nras neuroblastoma ras oncogene gene MP:0001263 weight loss IAGP N RGD:5509061 20180719 MGI PMID:22876308 11018 Nras neuroblastoma ras oncogene gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20180719 MGI PMID:25252692 11018 Nras neuroblastoma ras oncogene gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180719 MGI PMID:23303902 11018 Nras neuroblastoma ras oncogene gene MP:0001406 abnormal gait IAGP N RGD:5509061 20180719 MGI PMID:23303902 11018 Nras neuroblastoma ras oncogene gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 11018 Nras neuroblastoma ras oncogene gene MP:0001577 anemia IAGP N RGD:5509061 20180719 MGI PMID:23733505 11018 Nras neuroblastoma ras oncogene gene MP:0001577 anemia IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20180719 MGI PMID:21586752 11018 Nras neuroblastoma ras oncogene gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180719 MGI PMID:22876308 11018 Nras neuroblastoma ras oncogene gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20180719 MGI PMID:20179099 11018 Nras neuroblastoma ras oncogene gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20180719 MGI PMID:23303902 11018 Nras neuroblastoma ras oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:23303902 11018 Nras neuroblastoma ras oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:23733505 11018 Nras neuroblastoma ras oncogene gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20180719 MGI PMID:23733505 11018 Nras neuroblastoma ras oncogene gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:11238881 11018 Nras neuroblastoma ras oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:18059342 11018 Nras neuroblastoma ras oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:23418499 11018 Nras neuroblastoma ras oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:7878045 11018 Nras neuroblastoma ras oncogene gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0002652 thin myocardium IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20180719 MGI PMID:23303902 11018 Nras neuroblastoma ras oncogene gene MP:0002764 short tibia IEA N RGD:5509061 20220811 MGI 11018 Nras neuroblastoma ras oncogene gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20180719 MGI PMID:23303902 11018 Nras neuroblastoma ras oncogene gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0003717 pallor IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0003717 pallor IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20180719 MGI PMID:23303902 11018 Nras neuroblastoma ras oncogene gene MP:0004937 dilated heart IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20180719 MGI PMID:22876308 11018 Nras neuroblastoma ras oncogene gene MP:0005015 increased T cell number IAGP N RGD:5509061 20180719 MGI PMID:22876308 11018 Nras neuroblastoma ras oncogene gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20210128 MGI 11018 Nras neuroblastoma ras oncogene gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20180719 MGI PMID:22876308 11018 Nras neuroblastoma ras oncogene gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180719 MGI PMID:18372904 11018 Nras neuroblastoma ras oncogene gene MP:0009391 abnormal leptomeninges pigmentation IAGP N RGD:5509061 20180719 MGI PMID:23303902 11018 Nras neuroblastoma ras oncogene gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20180719 MGI PMID:23303902 11018 Nras neuroblastoma ras oncogene gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20200402 MGI PMID:27135738 11018 Nras neuroblastoma ras oncogene gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20180719 MGI PMID:25252692 11018 Nras neuroblastoma ras oncogene gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20180719 MGI PMID:23733505 11018 Nras neuroblastoma ras oncogene gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20180719 MGI PMID:23733505 11018 Nras neuroblastoma ras oncogene gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0010741 abnormal melanocyte proliferation IAGP N RGD:5509061 20180719 MGI PMID:23303902 11018 Nras neuroblastoma ras oncogene gene MP:0010741 abnormal melanocyte proliferation IAGP N RGD:5509061 20180719 MGI PMID:25252692 11018 Nras neuroblastoma ras oncogene gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:18059342 11018 Nras neuroblastoma ras oncogene gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:18059342 11018 Nras neuroblastoma ras oncogene gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:21586752 11018 Nras neuroblastoma ras oncogene gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:22876308 11018 Nras neuroblastoma ras oncogene gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:18059342 11018 Nras neuroblastoma ras oncogene gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0011246 abnormal fetal liver hematopoietic progenitor cell morphology IAGP N RGD:5509061 20231109 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0011995 decreased leukemia incidence IAGP N RGD:5509061 20211021 MGI PMID:26493479 11018 Nras neuroblastoma ras oncogene gene MP:0012080 chylous ascites IAGP N RGD:5509061 20180719 MGI PMID:20179099 11018 Nras neuroblastoma ras oncogene gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20180719 MGI PMID:9334313 11018 Nras neuroblastoma ras oncogene gene MP:0014518 myocardial hypertrabeculation IAGP N RGD:5509061 20240822 MGI PMID:33681212 11018 Nras neuroblastoma ras oncogene gene MP:0031555 abnormal pulmonary valve development IAGP N RGD:5509061 20240125 MGI PMID:33681212 11020 Nrdc nardilysin convertase gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19935654 11020 Nrdc nardilysin convertase gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:19935654 11020 Nrdc nardilysin convertase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19935654 11020 Nrdc nardilysin convertase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19935654 11020 Nrdc nardilysin convertase gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:19935654 11020 Nrdc nardilysin convertase gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:19935654 11020 Nrdc nardilysin convertase gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19935654 11020 Nrdc nardilysin convertase gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:19935654 11020 Nrdc nardilysin convertase gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19935654 11020 Nrdc nardilysin convertase gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:19935654 11020 Nrdc nardilysin convertase gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:19935654 11020 Nrdc nardilysin convertase gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:19935654 11020 Nrdc nardilysin convertase gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:19935654 11020 Nrdc nardilysin convertase gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19935654 11020 Nrdc nardilysin convertase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19935654 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16337809 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0000160 kyphosis IAGP N RGD:5509061 20170720 MGI PMID:25810523 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:16337809 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20170720 MGI PMID:25810523 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:8653786 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:8653786 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:16337809 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:8653786 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20170720 MGI PMID:25810523 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001054 failure of neuromuscular synapse presynaptic differentiation IAGP N RGD:5509061 20141003 MGI PMID:8653786 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001055 failure of neuromuscular synapse postsynaptic differentiation IAGP N RGD:5509061 20141003 MGI PMID:8653786 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170720 MGI PMID:25810523 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16337809 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20170720 MGI PMID:25810523 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:8653786 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:8653786 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8653786 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:8653786 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0001953 respiratory failure IAGP N RGD:5509061 20170720 MGI PMID:25810523 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20170720 MGI PMID:25810523 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16337809 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20170720 MGI PMID:25810523 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20170720 MGI PMID:25810523 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20170720 MGI PMID:25810523 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20170720 MGI PMID:25810523 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16337809 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:18718936 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20170720 MGI PMID:25810523 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170720 MGI PMID:25810523 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16337809 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8653786 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20141003 MGI PMID:16337809 11021 Musk muscle, skeletal, receptor tyrosine kinase gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20170720 MGI PMID:25810523 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:12925599 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20181227 MGI 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:23776632 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10798407 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20141003 MGI PMID:19158294 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:9728915 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10798407 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000910 small facial motor nucleus IAGP N RGD:5509061 20141003 MGI PMID:8402890 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:10571233 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:8402890 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000959 abnormal somatic sensory system morphology IAGP N RGD:5509061 20141003 MGI PMID:11877382 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000959 abnormal somatic sensory system morphology IAGP N RGD:5509061 20141003 MGI PMID:9728915 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:8402890 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:10725924 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:11877382 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:11877382 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12654337 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:16009525 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:7588071 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000972 abnormal mechanoreceptor morphology IAGP N RGD:5509061 20231026 MGI PMID:30126905 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0000980 absent hair-down neurons IAGP N RGD:5509061 20141003 MGI PMID:9728915 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001021 small L4 dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:12654337 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001072 abnormal vestibulocochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11877382 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:12654337 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:12654337 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:12654337 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:9728915 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:12654337 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:8402890 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:15013804 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23776632 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19158294 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11681842 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23776632 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10516311 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23776632 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11681842 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:10516311 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:19158294 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10725924 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:9728915 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18832146 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:23774276 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:10725924 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001411 spinning IAGP N RGD:5509061 20141003 MGI PMID:10725924 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001435 absent suckling reflex IAGP N RGD:5509061 20141003 MGI PMID:8402890 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001437 no swallowing reflex IAGP N RGD:5509061 20141003 MGI PMID:8402890 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001462 abnormal avoidance learning behavior IAGP N RGD:5509061 20141003 MGI PMID:10571233 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10571233 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:10571233 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10571233 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18832146 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:23064382 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001490 abnormal vibrissae reflex IAGP N RGD:5509061 20141003 MGI PMID:8402890 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001500 decreased kindling response IAGP N RGD:5509061 20141003 MGI PMID:15233915 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10516311 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23776632 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:12367511 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:10516311 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:10571233 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:10516311 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10571233 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15820690 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:21192928 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:21192928 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12367511 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:21192928 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002638 abnormal pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:10516311 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002664 decreased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:22232675 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:22232675 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:12654337 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15013804 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:10571233 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:18832146 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:19158294 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:7588071 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:7588071 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10798407 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:12367511 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21192928 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12925599 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003357 impaired granulosa cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15013804 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:23776632 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:23064382 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:23064382 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003986 small cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:12654337 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003986 small cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:7588071 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:12654337 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:7588071 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:9728915 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0003989 abnormal barrel cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16009525 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10516311 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0004220 abnormal peripheral nervous system regeneration IAGP N RGD:5509061 20141003 MGI PMID:11745667 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:7588071 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0004409 abnormal crista ampullaris neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7588071 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0004427 abnormal vestibular labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0004428 abnormal type I vestibular cell IAGP N RGD:5509061 20141003 MGI PMID:12925599 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0004716 abnormal cochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11877382 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0004718 abnormal vestibular nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11877382 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0004718 abnormal vestibular nerve morphology IAGP N RGD:5509061 20240801 MGI PMID:7588071 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0004747 abnormal cochlear OHC afferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12925599 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0004747 abnormal cochlear OHC afferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:7588071 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:22232675 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:11681842 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:23776632 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11681842 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17611278 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:10516311 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:10798407 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:17611278 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18832146 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19158294 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0008299 adrenal cortical hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:23064382 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:10516311 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:9728915 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23774276 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:10798407 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20160421 MGI 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:11877382 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:23776632 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:23774276 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:10516311 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18832146 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20150312 MGI PMID:25525881 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10516311 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11681842 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12654337 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15372074 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23776632 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22196735 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8402890 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:21192928 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:21192928 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0011987 abnormal GABAergic neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0014286 increased adrenal gland zona fasciculata size IAGP N RGD:5509061 20230907 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:12925599 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0014490 abnormal inner ear vestibular sensory neuron innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:11877382 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0014490 abnormal inner ear vestibular sensory neuron innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:12925599 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0014490 abnormal inner ear vestibular sensory neuron innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:7588071 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0014491 abnormal mammary gland sensory innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:23224557 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:24619096 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0031018 decreased granulosa cell proliferation IAGP N RGD:5509061 20200130 MGI PMID:15013804 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:15013804 11023 Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:23774276 11024 Nxph1 neurexophilin 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:9856994 11024 Nxph1 neurexophilin 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9856994 11027 Oca2 oculocutaneous albinism II gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:8389469 11027 Oca2 oculocutaneous albinism II gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15051828 11027 Oca2 oculocutaneous albinism II gene MP:0000184 abnormal circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15051828 11027 Oca2 oculocutaneous albinism II gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:12644183 11027 Oca2 oculocutaneous albinism II gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:13943454 11027 Oca2 oculocutaneous albinism II gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:1495987 11027 Oca2 oculocutaneous albinism II gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:1509264 11027 Oca2 oculocutaneous albinism II gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:8575552 11027 Oca2 oculocutaneous albinism II gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:8601493 11027 Oca2 oculocutaneous albinism II gene MP:0000421 mottled coat IAGP N RGD:5509061 20141003 MGI PMID:1673574 11027 Oca2 oculocutaneous albinism II gene MP:0000421 mottled coat IAGP N RGD:5509061 20141003 MGI PMID:5094803 11027 Oca2 oculocutaneous albinism II gene MP:0000423 delayed hair regrowth IEA N RGD:5509061 20111116 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0000427 abnormal hair cycle IEA N RGD:5509061 20111116 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:8601493 11027 Oca2 oculocutaneous albinism II gene MP:0001124 abnormal gametes IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:9689098 11027 Oca2 oculocutaneous albinism II gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15051828 11027 Oca2 oculocutaneous albinism II gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14402638 11027 Oca2 oculocutaneous albinism II gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8601493 11027 Oca2 oculocutaneous albinism II gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:13943454 11027 Oca2 oculocutaneous albinism II gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1673574 11027 Oca2 oculocutaneous albinism II gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8575552 11027 Oca2 oculocutaneous albinism II gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:9689098 11027 Oca2 oculocutaneous albinism II gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:14402638 11027 Oca2 oculocutaneous albinism II gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:9689098 11027 Oca2 oculocutaneous albinism II gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:14402638 11027 Oca2 oculocutaneous albinism II gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15051828 11027 Oca2 oculocutaneous albinism II gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15051828 11027 Oca2 oculocutaneous albinism II gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:1495987 11027 Oca2 oculocutaneous albinism II gene MP:0001922 reduced male fertility IEA N RGD:5509061 20111116 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14402638 11027 Oca2 oculocutaneous albinism II gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:7317942 11027 Oca2 oculocutaneous albinism II gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8601493 11027 Oca2 oculocutaneous albinism II gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8601493 11027 Oca2 oculocutaneous albinism II gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:9689098 11027 Oca2 oculocutaneous albinism II gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14402638 11027 Oca2 oculocutaneous albinism II gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:7317942 11027 Oca2 oculocutaneous albinism II gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8389469 11027 Oca2 oculocutaneous albinism II gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20111116 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1495987 11027 Oca2 oculocutaneous albinism II gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17247308 11027 Oca2 oculocutaneous albinism II gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8575552 11027 Oca2 oculocutaneous albinism II gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15051828 11027 Oca2 oculocutaneous albinism II gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15051828 11027 Oca2 oculocutaneous albinism II gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12644183 11027 Oca2 oculocutaneous albinism II gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:1495987 11027 Oca2 oculocutaneous albinism II gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8601493 11027 Oca2 oculocutaneous albinism II gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8601493 11027 Oca2 oculocutaneous albinism II gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8601493 11027 Oca2 oculocutaneous albinism II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14402638 11027 Oca2 oculocutaneous albinism II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7317942 11027 Oca2 oculocutaneous albinism II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8601493 11027 Oca2 oculocutaneous albinism II gene MP:0002089 abnormal postnatal growth/weight/body size IEA N RGD:5509061 20111116 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15051828 11027 Oca2 oculocutaneous albinism II gene MP:0002161 abnormal fertility/fecundity IEA N RGD:5509061 20111116 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20120126 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0002412 increased susceptibility to bacterial infection IEA N RGD:5509061 20111116 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15051828 11027 Oca2 oculocutaneous albinism II gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:11074018 11027 Oca2 oculocutaneous albinism II gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:15051828 11027 Oca2 oculocutaneous albinism II gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:8575552 11027 Oca2 oculocutaneous albinism II gene MP:0003171 phenotypic reversion IAGP N RGD:5509061 20141003 MGI PMID:1495987 11027 Oca2 oculocutaneous albinism II gene MP:0003171 phenotypic reversion IAGP N RGD:5509061 20141003 MGI PMID:1673574 11027 Oca2 oculocutaneous albinism II gene MP:0003171 phenotypic reversion IAGP N RGD:5509061 20141003 MGI PMID:8419934 11027 Oca2 oculocutaneous albinism II gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:8601493 11027 Oca2 oculocutaneous albinism II gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:11074018 11027 Oca2 oculocutaneous albinism II gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:15051828 11027 Oca2 oculocutaneous albinism II gene MP:0004381 abnormal hair follicle melanocyte morphology IEA N RGD:5509061 20141003 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11074018 11027 Oca2 oculocutaneous albinism II gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:15051828 11027 Oca2 oculocutaneous albinism II gene MP:0005072 abnormal hair follicle melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:17247308 11027 Oca2 oculocutaneous albinism II gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 11027 Oca2 oculocutaneous albinism II gene MP:0005077 abnormal melanogenesis IAGP N RGD:5509061 20141003 MGI PMID:4634048 11027 Oca2 oculocutaneous albinism II gene MP:0005114 premature hair loss IEA N RGD:5509061 20111116 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:14402638 11027 Oca2 oculocutaneous albinism II gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1495987 11027 Oca2 oculocutaneous albinism II gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1509264 11027 Oca2 oculocutaneous albinism II gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1673574 11027 Oca2 oculocutaneous albinism II gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8601493 11027 Oca2 oculocutaneous albinism II gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15051828 11027 Oca2 oculocutaneous albinism II gene MP:0005366 variegated coat color IAGP N RGD:5509061 20141003 MGI PMID:1673574 11027 Oca2 oculocutaneous albinism II gene MP:0005409 darkened coat color IEA N RGD:5509061 20111116 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:1495987 11027 Oca2 oculocutaneous albinism II gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:14402638 11027 Oca2 oculocutaneous albinism II gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:7317942 11027 Oca2 oculocutaneous albinism II gene MP:0006159 ocular albinism IEA N RGD:5509061 20111116 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0008480 absent eye pigmentation IEA N RGD:5509061 20111116 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20180927 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11074018 11027 Oca2 oculocutaneous albinism II gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15051828 11027 Oca2 oculocutaneous albinism II gene MP:0008912 nervous IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0009233 enlarged sperm head IAGP N RGD:5509061 20141003 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0009554 abnormal hair follicle melanin granule shape IAGP N RGD:5509061 20141003 MGI PMID:17247308 11027 Oca2 oculocutaneous albinism II gene MP:0009555 abnormal hair follicle melanin granule distribution IAGP N RGD:5509061 20141003 MGI PMID:17247308 11027 Oca2 oculocutaneous albinism II gene MP:0010193 abnormal choroid melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 11027 Oca2 oculocutaneous albinism II gene MP:0010389 mosaic coat color IEA N RGD:5509061 20150507 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0010766 abnormal NK cell physiology IEA N RGD:5509061 20111116 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8601493 11027 Oca2 oculocutaneous albinism II gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7317942 11027 Oca2 oculocutaneous albinism II gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8601493 11027 Oca2 oculocutaneous albinism II gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8601493 11027 Oca2 oculocutaneous albinism II gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1495987 11027 Oca2 oculocutaneous albinism II gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11074018 11027 Oca2 oculocutaneous albinism II gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15051828 11027 Oca2 oculocutaneous albinism II gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8601493 11027 Oca2 oculocutaneous albinism II gene MP:0011277 decreased tail pigmentation IEA N RGD:5509061 20120126 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0011279 decreased ear pigmentation IEA N RGD:5509061 20141003 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0011400 lethality, complete penetrance IEA N RGD:5509061 20120126 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0011627 decreased skin pigmentation IEA N RGD:5509061 20141003 MGI 11027 Oca2 oculocutaneous albinism II gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:5565073 11027 Oca2 oculocutaneous albinism II gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:9689098 11028 Ocm oncomodulin gene MP:0001967 deafness IEA N RGD:5509061 20111116 MGI 11028 Ocm oncomodulin gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20190613 MGI PMID:26843644 11028 Ocm oncomodulin gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20190613 MGI PMID:26843644 11028 Ocm oncomodulin gene MP:0004586 pillar cell degeneration IAGP N RGD:5509061 20190613 MGI PMID:26843644 11028 Ocm oncomodulin gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20190613 MGI PMID:26843644 11028 Ocm oncomodulin gene MP:0006325 impaired hearing IAGP N RGD:5509061 20190613 MGI PMID:26843644 11028 Ocm oncomodulin gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20170105 MGI 11028 Ocm oncomodulin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20190613 MGI PMID:26843644 11028 Ocm oncomodulin gene MP:0011968 decreased threshold for auditory brainstem response IAGP N RGD:5509061 20190613 MGI PMID:26843644 11032 Odf1 outer dense fiber of sperm tails 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 11032 Odf1 outer dense fiber of sperm tails 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22037768 11032 Odf1 outer dense fiber of sperm tails 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22037768 11032 Odf1 outer dense fiber of sperm tails 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22037768 11032 Odf1 outer dense fiber of sperm tails 1 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:22037768 11032 Odf1 outer dense fiber of sperm tails 1 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20211021 MGI 11032 Odf1 outer dense fiber of sperm tails 1 gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:22037768 11032 Odf1 outer dense fiber of sperm tails 1 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:22037768 11032 Odf1 outer dense fiber of sperm tails 1 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:22037768 11032 Odf1 outer dense fiber of sperm tails 1 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:22037768 11034 Omp olfactory marker protein gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:15157418 11034 Omp olfactory marker protein gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17537788 11034 Omp olfactory marker protein gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:21613506 11034 Omp olfactory marker protein gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20161229 MGI PMID:23884929 11034 Omp olfactory marker protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22057188 11034 Omp olfactory marker protein gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20210805 MGI PMID:34186026 11034 Omp olfactory marker protein gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:22057188 11034 Omp olfactory marker protein gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:23637188 11034 Omp olfactory marker protein gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:8790421 11034 Omp olfactory marker protein gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:21613506 11034 Omp olfactory marker protein gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20160623 MGI PMID:26046438 11034 Omp olfactory marker protein gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 11034 Omp olfactory marker protein gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20161229 MGI PMID:21957232 11034 Omp olfactory marker protein gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:8790421 11034 Omp olfactory marker protein gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20161229 MGI PMID:23884929 11034 Omp olfactory marker protein gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20180322 MGI PMID:29118104 11034 Omp olfactory marker protein gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20180322 MGI PMID:29118104 11034 Omp olfactory marker protein gene MP:0003462 abnormal response to novel odor IAGP N RGD:5509061 20210805 MGI PMID:34186026 11034 Omp olfactory marker protein gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20191226 MGI PMID:31653840 11034 Omp olfactory marker protein gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15157418 11034 Omp olfactory marker protein gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17493809 11034 Omp olfactory marker protein gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17537788 11034 Omp olfactory marker protein gene MP:0005499 abnormal olfactory system morphology IAGP N RGD:5509061 20141003 MGI PMID:23637188 11034 Omp olfactory marker protein gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:8790421 11034 Omp olfactory marker protein gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17521568 11034 Omp olfactory marker protein gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23035080 11034 Omp olfactory marker protein gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20161229 MGI PMID:23884929 11034 Omp olfactory marker protein gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20180322 MGI PMID:29118104 11034 Omp olfactory marker protein gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:22057188 11034 Omp olfactory marker protein gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:23637188 11034 Omp olfactory marker protein gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20161229 MGI PMID:23884929 11034 Omp olfactory marker protein gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20171116 MGI PMID:28495971 11034 Omp olfactory marker protein gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20180322 MGI PMID:29118104 11034 Omp olfactory marker protein gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20161229 MGI PMID:23884929 11034 Omp olfactory marker protein gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:23637188 11034 Omp olfactory marker protein gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20180322 MGI PMID:29118104 11034 Omp olfactory marker protein gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23035080 11034 Omp olfactory marker protein gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20161229 MGI PMID:21957232 11034 Omp olfactory marker protein gene MP:0009946 abnormal olfactory bulb layer morphology IAGP N RGD:5509061 20161229 MGI PMID:23884929 11034 Omp olfactory marker protein gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20161229 MGI PMID:23884929 11034 Omp olfactory marker protein gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20180322 MGI PMID:29118104 11034 Omp olfactory marker protein gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20190425 MGI PMID:28815295 11034 Omp olfactory marker protein gene MP:0010055 abnormal sensory neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22057188 11034 Omp olfactory marker protein gene MP:0010057 abnormal olfactory bulb outer nerve layer morphology IAGP N RGD:5509061 20161229 MGI PMID:23884929 11034 Omp olfactory marker protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180322 MGI PMID:29118104 11034 Omp olfactory marker protein gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:23637188 11034 Omp olfactory marker protein gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20161229 MGI PMID:21957232 11034 Omp olfactory marker protein gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20171116 MGI PMID:28495971 11034 Omp olfactory marker protein gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20180322 MGI PMID:29118104 11034 Omp olfactory marker protein gene MP:0011678 abnormal vomeronasal sensory neuron physiology IAGP N RGD:5509061 20191226 MGI PMID:31653840 11034 Omp olfactory marker protein gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:23035080 11034 Omp olfactory marker protein gene MP:0012020 abnormal olfactory epithelium physiology IAGP N RGD:5509061 20180322 MGI PMID:29118104 11034 Omp olfactory marker protein gene MP:0020348 decreased olfactory sensory neuron number IAGP N RGD:5509061 20161229 MGI PMID:21957232 11034 Omp olfactory marker protein gene MP:0020348 decreased olfactory sensory neuron number IAGP N RGD:5509061 20161229 MGI PMID:23884929 11034 Omp olfactory marker protein gene MP:0020348 decreased olfactory sensory neuron number IAGP N RGD:5509061 20180322 MGI PMID:29118104 11034 Omp olfactory marker protein gene MP:0020852 abnormal olfactory behavior IAGP N RGD:5509061 20240229 MGI PMID:36330924 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:16467704 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:16564235 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16467704 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16564235 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:16467704 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:16467704 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:16564235 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:9573043 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:9647741 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:11160187 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16564235 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:9573043 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:9647741 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:16467704 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:9573043 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:9647741 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9573043 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9647741 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9573043 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16840715 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:11160187 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:11160187 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0000774 decreased brain size IEA N RGD:5509061 20210520 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12446599 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9573043 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0001314 cornea opacity IEA N RGD:5509061 20201022 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:16564235 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:16564235 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210520 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9647741 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:11160187 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:16467704 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:16564235 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210520 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:11160187 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11160187 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:16467704 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9647741 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0003068 enlarged kidney IEA N RGD:5509061 20201022 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:12446599 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11160187 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:11160187 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16564235 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11160187 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9573043 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0004290 abnormal stapes footplate morphology IAGP N RGD:5509061 20141003 MGI PMID:16467704 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0004290 abnormal stapes footplate morphology IAGP N RGD:5509061 20141003 MGI PMID:16564235 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:16467704 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:16467704 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0004897 otosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16467704 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:9573043 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:12446599 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:9573043 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11160187 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12446599 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16564235 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:16564235 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:16840715 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0006133 calcified artery IAGP N RGD:5509061 20141003 MGI PMID:9573043 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:11160187 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11160187 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11160187 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0008233 abnormal pro-B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11160187 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:16564235 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:9647741 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0009084 blind uterus IEA N RGD:5509061 20210826 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0010663 abnormal brachiocephalic trunk morphology IAGP N RGD:5509061 20141003 MGI PMID:16840715 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0010870 absent bone trabeculae IAGP N RGD:5509061 20141003 MGI PMID:9573043 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:9573043 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9573043 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9647741 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16467704 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16564235 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:16467704 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0030281 thin parietal bone IAGP N RGD:5509061 20171102 MGI PMID:9573043 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0030399 abnormal incus body morphology IAGP N RGD:5509061 20171207 MGI PMID:16564235 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0030400 abnormal stapes annular ligament morphology IAGP N RGD:5509061 20171207 MGI PMID:16564235 11035 Tnfrsf11b tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) gene MP:0030793 short femur neck IAGP N RGD:5509061 20181018 MGI PMID:11160187 11036 Oprd1 opioid receptor, delta 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10835636 11036 Oprd1 opioid receptor, delta 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10835636 11036 Oprd1 opioid receptor, delta 1 gene MP:0001980 abnormal chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:12486185 11036 Oprd1 opioid receptor, delta 1 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:21295407 11036 Oprd1 opioid receptor, delta 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20111116 MGI 11036 Oprd1 opioid receptor, delta 1 gene MP:0003064 decreased coping response IAGP N RGD:5509061 20141003 MGI PMID:10835636 11036 Oprd1 opioid receptor, delta 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17544222 11036 Oprd1 opioid receptor, delta 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21295407 11036 Oprd1 opioid receptor, delta 1 gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:12486185 11036 Oprd1 opioid receptor, delta 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20141003 MGI PMID:17544222 11036 Oprd1 opioid receptor, delta 1 gene MP:0009778 impaired behavioral response to anesthetic IAGP N RGD:5509061 20141003 MGI PMID:17544222 11038694 Pas19_m pulmonary adenoma susceptibility 19 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20160219 MGI Created by mouse qtl pipeline PMID:12810665 11038694 Pas19_m pulmonary adenoma susceptibility 19 (mouse) qtl MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20160225 MGI PMID:7813906 11038694 Pas19_m pulmonary adenoma susceptibility 19 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12810665 11038830 Trdn triadin gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20160304 MGI PMID:19843516 11038830 Trdn triadin gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20160304 MGI PMID:19843516 11038830 Trdn triadin gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20160304 MGI PMID:19843516 11038830 Trdn triadin gene MP:0009411 abnormal skeletal muscle fiber triad morphology IAGP N RGD:5509061 20160304 MGI PMID:17981799 11038830 Trdn triadin gene MP:0009411 abnormal skeletal muscle fiber triad morphology IAGP N RGD:5509061 20160304 MGI PMID:19843516 11038830 Trdn triadin gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20160304 MGI PMID:19843516 11038830 Trdn triadin gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160304 MGI PMID:19843516 11039 Otc ornithine transcarbamylase gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0000414 alopecia IEA N RGD:5509061 20111116 MGI 11039 Otc ornithine transcarbamylase gene MP:0000416 sparse hair IAGP N RGD:5509061 20180719 MGI PMID:25647322 11039 Otc ornithine transcarbamylase gene MP:0000416 sparse hair IAGP N RGD:5509061 20180719 MGI PMID:3162766 11039 Otc ornithine transcarbamylase gene MP:0000416 sparse hair IAGP N RGD:5509061 20180719 MGI PMID:4603259 11039 Otc ornithine transcarbamylase gene MP:0000416 sparse hair IAGP N RGD:5509061 20180719 MGI PMID:5727 11039 Otc ornithine transcarbamylase gene MP:0000416 sparse hair IAGP N RGD:5509061 20180719 MGI PMID:7707692 11039 Otc ornithine transcarbamylase gene MP:0000416 sparse hair IAGP N RGD:5509061 20180719 MGI PMID:8461026 11039 Otc ornithine transcarbamylase gene MP:0000416 sparse hair IAGP N RGD:5509061 20180719 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0000418 focal hair loss IEA N RGD:5509061 20111116 MGI 11039 Otc ornithine transcarbamylase gene MP:0000422 delayed hair appearance IEA N RGD:5509061 20111116 MGI 11039 Otc ornithine transcarbamylase gene MP:0000436 abnormal head movements IAGP N RGD:5509061 20180719 MGI PMID:1531355 11039 Otc ornithine transcarbamylase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180719 MGI PMID:7707692 11039 Otc ornithine transcarbamylase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180719 MGI PMID:8108192 11039 Otc ornithine transcarbamylase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180719 MGI PMID:2920015 11039 Otc ornithine transcarbamylase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220519 MGI 11039 Otc ornithine transcarbamylase gene MP:0000745 tremors IAGP N RGD:5509061 20180719 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0000774 decreased brain size IAGP N RGD:5509061 20180719 MGI PMID:9630607 11039 Otc ornithine transcarbamylase gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20180719 MGI PMID:7816342 11039 Otc ornithine transcarbamylase gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20180719 MGI PMID:8108192 11039 Otc ornithine transcarbamylase gene MP:0001194 dermatitis IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20180719 MGI PMID:3162766 11039 Otc ornithine transcarbamylase gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20180719 MGI PMID:5727 11039 Otc ornithine transcarbamylase gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20180719 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0001212 skin lesions IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0001263 weight loss IAGP N RGD:5509061 20180719 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20180719 MGI PMID:16497529 11039 Otc ornithine transcarbamylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20180719 MGI PMID:25647322 11039 Otc ornithine transcarbamylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20180719 MGI PMID:5727 11039 Otc ornithine transcarbamylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20180719 MGI PMID:7707692 11039 Otc ornithine transcarbamylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20180719 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0001394 circling IAGP N RGD:5509061 20180719 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20180719 MGI PMID:7707692 11039 Otc ornithine transcarbamylase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180719 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20180719 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20180719 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20180719 MGI PMID:16497529 11039 Otc ornithine transcarbamylase gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20111116 MGI 11039 Otc ornithine transcarbamylase gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20220519 MGI 11039 Otc ornithine transcarbamylase gene MP:0001577 anemia IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20180719 MGI PMID:7827141 11039 Otc ornithine transcarbamylase gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20180719 MGI PMID:1531355 11039 Otc ornithine transcarbamylase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20180719 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20180719 MGI PMID:4603259 11039 Otc ornithine transcarbamylase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20180719 MGI PMID:25647322 11039 Otc ornithine transcarbamylase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20180719 MGI PMID:5727 11039 Otc ornithine transcarbamylase gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:8461026 11039 Otc ornithine transcarbamylase gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20180719 MGI PMID:8108192 11039 Otc ornithine transcarbamylase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180719 MGI PMID:1531355 11039 Otc ornithine transcarbamylase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180719 MGI PMID:7707692 11039 Otc ornithine transcarbamylase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180719 MGI PMID:7816342 11039 Otc ornithine transcarbamylase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180719 MGI PMID:8041507 11039 Otc ornithine transcarbamylase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180719 MGI PMID:8108192 11039 Otc ornithine transcarbamylase gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0002493 increased IgG level IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220519 MGI 11039 Otc ornithine transcarbamylase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180719 MGI PMID:2920015 11039 Otc ornithine transcarbamylase gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0003415 priapism IAGP N RGD:5509061 20180719 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20180719 MGI PMID:1627360 11039 Otc ornithine transcarbamylase gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20180719 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20180719 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20180719 MGI PMID:7827141 11039 Otc ornithine transcarbamylase gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20180719 MGI PMID:1575747 11039 Otc ornithine transcarbamylase gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20180719 MGI PMID:8424807 11039 Otc ornithine transcarbamylase gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20180719 MGI PMID:1575747 11039 Otc ornithine transcarbamylase gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20180719 MGI PMID:16497529 11039 Otc ornithine transcarbamylase gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20180719 MGI PMID:3162766 11039 Otc ornithine transcarbamylase gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20180719 MGI PMID:7707692 11039 Otc ornithine transcarbamylase gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20180719 MGI PMID:7816342 11039 Otc ornithine transcarbamylase gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20180719 MGI PMID:8424807 11039 Otc ornithine transcarbamylase gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20180719 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20180719 MGI PMID:25647322 11039 Otc ornithine transcarbamylase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20180719 MGI PMID:7707692 11039 Otc ornithine transcarbamylase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20180719 MGI PMID:7828023 11039 Otc ornithine transcarbamylase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20180719 MGI PMID:1575747 11039 Otc ornithine transcarbamylase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20180719 MGI PMID:25647322 11039 Otc ornithine transcarbamylase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20180719 MGI PMID:7828023 11039 Otc ornithine transcarbamylase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180719 MGI PMID:2920015 11039 Otc ornithine transcarbamylase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180719 MGI PMID:7707692 11039 Otc ornithine transcarbamylase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180719 MGI PMID:7816342 11039 Otc ornithine transcarbamylase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180719 MGI PMID:8041507 11039 Otc ornithine transcarbamylase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180719 MGI PMID:8424807 11039 Otc ornithine transcarbamylase gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180719 MGI PMID:2920015 11039 Otc ornithine transcarbamylase gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20180719 MGI PMID:9630607 11039 Otc ornithine transcarbamylase gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20180719 MGI PMID:16497529 11039 Otc ornithine transcarbamylase gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20180719 MGI PMID:16497529 11039 Otc ornithine transcarbamylase gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20180719 MGI PMID:2920015 11039 Otc ornithine transcarbamylase gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20180719 MGI PMID:16497529 11039 Otc ornithine transcarbamylase gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20180719 MGI PMID:25647322 11039 Otc ornithine transcarbamylase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180719 MGI PMID:7827141 11039 Otc ornithine transcarbamylase gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20180719 MGI PMID:9630607 11039 Otc ornithine transcarbamylase gene MP:0010028 aciduria IAGP N RGD:5509061 20180719 MGI PMID:8461026 11039 Otc ornithine transcarbamylase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:7930593 11039 Otc ornithine transcarbamylase gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20180719 MGI PMID:9630607 11039 Otc ornithine transcarbamylase gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20180719 MGI 11039 Otc ornithine transcarbamylase gene MP:0011588 decreased ornithine carbamoyltransferase activity IAGP N RGD:5509061 20180719 MGI PMID:3981356 11039 Otc ornithine transcarbamylase gene MP:0011588 decreased ornithine carbamoyltransferase activity IAGP N RGD:5509061 20180719 MGI PMID:5727 11039 Otc ornithine transcarbamylase gene MP:0011588 decreased ornithine carbamoyltransferase activity IAGP N RGD:5509061 20180719 MGI PMID:6623083 11039 Otc ornithine transcarbamylase gene MP:0011588 decreased ornithine carbamoyltransferase activity IAGP N RGD:5509061 20180719 MGI PMID:7707692 11039 Otc ornithine transcarbamylase gene MP:0011588 decreased ornithine carbamoyltransferase activity IAGP N RGD:5509061 20180719 MGI PMID:7816342 11039 Otc ornithine transcarbamylase gene MP:0011588 decreased ornithine carbamoyltransferase activity IAGP N RGD:5509061 20180719 MGI PMID:7828023 11039 Otc ornithine transcarbamylase gene MP:0011626 orotic acid urinary bladder stones IAGP N RGD:5509061 20180719 MGI PMID:5727 11039 Otc ornithine transcarbamylase gene MP:0011765 oroticaciduria IAGP N RGD:5509061 20180719 MGI PMID:3162766 11039 Otc ornithine transcarbamylase gene MP:0011765 oroticaciduria IAGP N RGD:5509061 20180719 MGI PMID:7707692 11039 Otc ornithine transcarbamylase gene MP:0011765 oroticaciduria IAGP N RGD:5509061 20180719 MGI PMID:7827141 11039 Otc ornithine transcarbamylase gene MP:0011765 oroticaciduria IAGP N RGD:5509061 20180719 MGI PMID:8221965 11039 Otc ornithine transcarbamylase gene MP:0011765 oroticaciduria IAGP N RGD:5509061 20180719 MGI PMID:8461026 11039 Otc ornithine transcarbamylase gene MP:0011765 oroticaciduria IAGP N RGD:5509061 20180920 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0020837 decreased circulating citrulline level IAGP N RGD:5509061 20180913 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0030648 decreased ornithine level IAGP N RGD:5509061 20180913 MGI PMID:7828023 11039 Otc ornithine transcarbamylase gene MP:0030651 decreased circulating ornithine level IAGP N RGD:5509061 20180913 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0030662 decreased circulating arginine level IAGP N RGD:5509061 20180913 MGI PMID:8750014 11039 Otc ornithine transcarbamylase gene MP:0030706 increased glutamine level IAGP N RGD:5509061 20180920 MGI PMID:1575747 11039 Otc ornithine transcarbamylase gene MP:0030709 increased circulating glutamine level IAGP N RGD:5509061 20180920 MGI PMID:1575747 11039 Otc ornithine transcarbamylase gene MP:0030709 increased circulating glutamine level IAGP N RGD:5509061 20180920 MGI PMID:8750014 11040 Oxt oxytocin gene MP:0001261 obese IAGP N RGD:5509061 20150129 MGI PMID:25157144 11040 Oxt oxytocin gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:16249339 11040 Oxt oxytocin gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:10888874 11040 Oxt oxytocin gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12746288 11040 Oxt oxytocin gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:8876199 11040 Oxt oxytocin gene MP:0001422 abnormal drinking behavior IAGP N RGD:5509061 20141003 MGI PMID:11573985 11040 Oxt oxytocin gene MP:0001432 abnormal food preference IAGP N RGD:5509061 20141003 MGI PMID:11573985 11040 Oxt oxytocin gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:9181490 11040 Oxt oxytocin gene MP:0001460 abnormal olfactory discrimination memory IAGP N RGD:5509061 20141003 MGI PMID:10888874 11040 Oxt oxytocin gene MP:0001460 abnormal olfactory discrimination memory IAGP N RGD:5509061 20141003 MGI PMID:11588199 11040 Oxt oxytocin gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12531722 11040 Oxt oxytocin gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:12531722 11040 Oxt oxytocin gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:10026810 11040 Oxt oxytocin gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:8933362 11040 Oxt oxytocin gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:10888874 11040 Oxt oxytocin gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20141003 MGI PMID:17895964 11040 Oxt oxytocin gene MP:0003838 abnormal milk ejection IAGP N RGD:5509061 20141003 MGI PMID:8876199 11040 Oxt oxytocin gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:9181490 11040 Oxt oxytocin gene MP:0004184 abnormal baroreceptor physiology IAGP N RGD:5509061 20141003 MGI PMID:12531722 11040 Oxt oxytocin gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:23028821 11040 Oxt oxytocin gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:10026810 11040 Oxt oxytocin gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:9181490 11040 Oxt oxytocin gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:23028821 11040 Oxt oxytocin gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:10026810 11040 Oxt oxytocin gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:17895964 11040 Oxt oxytocin gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:9751758 11040 Oxt oxytocin gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23028821 11040 Oxt oxytocin gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:9751758 11040 Oxt oxytocin gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:15718385 11040 Oxt oxytocin gene MP:0012008 delayed parturition IAGP N RGD:5509061 20191219 MGI PMID:9751758 11040 Oxt oxytocin gene MP:0013718 galactostasis IAGP N RGD:5509061 20150409 MGI PMID:10026810 11040 Oxt oxytocin gene MP:0013718 galactostasis IAGP N RGD:5509061 20150409 MGI PMID:8933362 11040 Oxt oxytocin gene MP:0014441 decreased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:23028821 11040 Oxt oxytocin gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:11573985 11040 Oxt oxytocin gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:17895964 11040464 Gm30731 predicted gene, 30731 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20200130 MGI PMID:31112699 11040464 Gm30731 predicted gene, 30731 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20200130 MGI PMID:31112699 11040464 Gm30731 predicted gene, 30731 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20200130 MGI PMID:31112699 11040464 Gm30731 predicted gene, 30731 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20200130 MGI PMID:31112699 11040464 Gm30731 predicted gene, 30731 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20200130 MGI PMID:31112699 11040464 Gm30731 predicted gene, 30731 gene MP:0012204 abnormal neuronal stem cell physiology IAGP N RGD:5509061 20200130 MGI PMID:31112699 11041 Oxtr oxytocin receptor gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20211021 MGI 11041 Oxtr oxytocin receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18356275 11041 Oxtr oxytocin receptor gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:16249339 11041 Oxtr oxytocin receptor gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:16249339 11041 Oxtr oxytocin receptor gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:18356275 11041 Oxtr oxytocin receptor gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:23872596 11041 Oxtr oxytocin receptor gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:16249339 11041 Oxtr oxytocin receptor gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:16249339 11041 Oxtr oxytocin receptor gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23872596 11041 Oxtr oxytocin receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18356275 11041 Oxtr oxytocin receptor gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:23872596 11041 Oxtr oxytocin receptor gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:18356275 11041 Oxtr oxytocin receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18356275 11041 Oxtr oxytocin receptor gene MP:0003838 abnormal milk ejection IAGP N RGD:5509061 20141003 MGI PMID:18356275 11041 Oxtr oxytocin receptor gene MP:0009326 absent maternal crouching IAGP N RGD:5509061 20141003 MGI PMID:16249339 11041 Oxtr oxytocin receptor gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:16249339 11041 Oxtr oxytocin receptor gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:16249339 11041 Oxtr oxytocin receptor gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:16249339 11042 P2rx1 purinergic receptor P2X, ligand-gated ion channel, 1 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:10638758 11042 P2rx1 purinergic receptor P2X, ligand-gated ion channel, 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10638758 11042 P2rx1 purinergic receptor P2X, ligand-gated ion channel, 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10638758 11042 P2rx1 purinergic receptor P2X, ligand-gated ion channel, 1 gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:10638758 11042 P2rx1 purinergic receptor P2X, ligand-gated ion channel, 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:10638758 11043 P2ry1 purinergic receptor P2Y, G-protein coupled 1 gene MP:0003422 abnormal thrombolysis IAGP N RGD:5509061 20141003 MGI PMID:10502826 11043 P2ry1 purinergic receptor P2Y, G-protein coupled 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:10502826 11043 P2ry1 purinergic receptor P2Y, G-protein coupled 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:10606627 11043 P2ry1 purinergic receptor P2Y, G-protein coupled 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:10502826 11043 P2ry1 purinergic receptor P2Y, G-protein coupled 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:10606627 11043 P2ry1 purinergic receptor P2Y, G-protein coupled 1 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201001 MGI PMID:10606627 11045 P2rx6 purinergic receptor P2X, ligand-gated ion channel, 6 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20141003 MGI 11045 P2rx6 purinergic receptor P2X, ligand-gated ion channel, 6 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20141003 MGI 11046 P4hb prolyl 4-hydroxylase, beta polypeptide gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23460613 11046 P4hb prolyl 4-hydroxylase, beta polypeptide gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 11046 P4hb prolyl 4-hydroxylase, beta polypeptide gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20191205 MGI PMID:26529254 11046 P4hb prolyl 4-hydroxylase, beta polypeptide gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:23460613 11046 P4hb prolyl 4-hydroxylase, beta polypeptide gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20191205 MGI PMID:26529254 11046 P4hb prolyl 4-hydroxylase, beta polypeptide gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20191205 MGI PMID:26529254 11046 P4hb prolyl 4-hydroxylase, beta polypeptide gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 11046 P4hb prolyl 4-hydroxylase, beta polypeptide gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 11046 P4hb prolyl 4-hydroxylase, beta polypeptide gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:26529254 11049307 Cdiptos CDIP transferase, opposite strand gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20240801 MGI PMID:35122073 11050 Pah phenylalanine hydroxylase gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 11050 Pah phenylalanine hydroxylase gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:8375656 11050 Pah phenylalanine hydroxylase gene MP:0000692 small spleen IEA N RGD:5509061 20220519 MGI 11050 Pah phenylalanine hydroxylase gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21640623 11050 Pah phenylalanine hydroxylase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 11050 Pah phenylalanine hydroxylase gene MP:0001297 microphthalmia IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0001304 cataract IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 11050 Pah phenylalanine hydroxylase gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0001460 abnormal olfactory discrimination memory IAGP N RGD:5509061 20141003 MGI PMID:10407053 11050 Pah phenylalanine hydroxylase gene MP:0001496 audiogenic seizures IEA N RGD:5509061 20111116 MGI 11050 Pah phenylalanine hydroxylase gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:8375656 11050 Pah phenylalanine hydroxylase gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:8375656 11050 Pah phenylalanine hydroxylase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8375656 11050 Pah phenylalanine hydroxylase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230601 MGI PMID:11487255 11050 Pah phenylalanine hydroxylase gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 11050 Pah phenylalanine hydroxylase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10767173 11050 Pah phenylalanine hydroxylase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8375656 11050 Pah phenylalanine hydroxylase gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:10407053 11050 Pah phenylalanine hydroxylase gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:8375656 11050 Pah phenylalanine hydroxylase gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 11050 Pah phenylalanine hydroxylase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0002204 abnormal synaptic neurotransmitter level IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0002768 small adrenal glands IEA N RGD:5509061 20220519 MGI 11050 Pah phenylalanine hydroxylase gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:8375656 11050 Pah phenylalanine hydroxylase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:10767173 11050 Pah phenylalanine hydroxylase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:2308957 11050 Pah phenylalanine hydroxylase gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:21640623 11050 Pah phenylalanine hydroxylase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:8375656 11050 Pah phenylalanine hydroxylase gene MP:0008732 reduced hair shaft melanin granule number IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0009358 environmentally induced seizures IEA N RGD:5509061 20111116 MGI 11050 Pah phenylalanine hydroxylase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8375656 11050 Pah phenylalanine hydroxylase gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:12499868 11050 Pah phenylalanine hydroxylase gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0013438 dysmyelination IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0013724 decreased circulating tyrosine level IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0020875 decreased nervous system dopamine level IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0030670 increased circulating phenylalanine level IAGP N RGD:5509061 20180920 MGI PMID:8375656 11050 Pah phenylalanine hydroxylase gene MP:0030670 increased circulating phenylalanine level IAGP N RGD:5509061 20210617 MGI PMID:33790381 11050 Pah phenylalanine hydroxylase gene MP:0030697 increased phenylalanine level IAGP N RGD:5509061 20180920 MGI PMID:21640623 11050 Pah phenylalanine hydroxylase gene MP:0030697 increased phenylalanine level IAGP N RGD:5509061 20210617 MGI PMID:33790381 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20201022 MGI 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:15869599 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20201022 MGI 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:8550840 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20200625 MGI PMID:23919993 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:14747283 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:16735799 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15869599 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15869599 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16735799 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16735799 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:15297377 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11481248 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16735799 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:11141484 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16735799 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:11104787 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17723219 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:15869599 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:11696429 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:12897066 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:16735799 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:12897066 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15297377 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17561000 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:15869599 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10712412 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16735799 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:14747283 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11481248 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16735799 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:10712412 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:14747283 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:14747283 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16735799 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:15869599 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16735799 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17561000 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11557572 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11059781 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:14747283 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:15869599 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20160512 MGI PMID:25799354 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:15869599 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:11481248 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:14747283 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14747283 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17723219 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20160512 MGI PMID:25799354 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:12897066 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200625 MGI PMID:23919993 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200625 MGI PMID:23919993 11055 Serpine1 serine (or cysteine) peptidase inhibitor, clade E, member 1 gene MP:0031414 decreased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:14747283 11056 Pam peptidylglycine alpha-amidating monooxygenase gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16225857 11056 Pam peptidylglycine alpha-amidating monooxygenase gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16225857 11056 Pam peptidylglycine alpha-amidating monooxygenase gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16225857 11056 Pam peptidylglycine alpha-amidating monooxygenase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16225857 11056 Pam peptidylglycine alpha-amidating monooxygenase gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16225857 11056 Pam peptidylglycine alpha-amidating monooxygenase gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 11056 Pam peptidylglycine alpha-amidating monooxygenase gene MP:0010943 abnormal bronchus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16225857 11056 Pam peptidylglycine alpha-amidating monooxygenase gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16225857 11056 Pam peptidylglycine alpha-amidating monooxygenase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11056 Pam peptidylglycine alpha-amidating monooxygenase gene MP:0012303 umbilical vein stenosis IAGP N RGD:5509061 20141003 MGI PMID:16225857 11057 Reg3b regenerating islet-derived 3 beta gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 11057 Reg3b regenerating islet-derived 3 beta gene MP:0000601 small liver IEA N RGD:5509061 20230601 MGI 11057 Reg3b regenerating islet-derived 3 beta gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 11057 Reg3b regenerating islet-derived 3 beta gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 11057 Reg3b regenerating islet-derived 3 beta gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 11057 Reg3b regenerating islet-derived 3 beta gene MP:0001148 enlarged testis IEA N RGD:5509061 20230601 MGI 11057 Reg3b regenerating islet-derived 3 beta gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20141003 MGI 11057 Reg3b regenerating islet-derived 3 beta gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 11058 Pax1 paired box 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7875377 11058 Pax1 paired box 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20150528 MGI PMID:8187635 11058 Pax1 paired box 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20200123 MGI PMID:24538930 11058 Pax1 paired box 1 gene MP:0000139 absent vertebral transverse processes IAGP N RGD:5509061 20141003 MGI PMID:7875377 11058 Pax1 paired box 1 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:10656775 11058 Pax1 paired box 1 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20200123 MGI PMID:24538930 11058 Pax1 paired box 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20200123 MGI PMID:24538930 11058 Pax1 paired box 1 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:19378260 11058 Pax1 paired box 1 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23377878 11058 Pax1 paired box 1 gene MP:0000454 abnormal jaw morphology IEA N RGD:5509061 20111116 MGI 11058 Pax1 paired box 1 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:16315099 11058 Pax1 paired box 1 gene MP:0000564 syndactyly IEA N RGD:5509061 20111116 MGI 11058 Pax1 paired box 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:19378260 11058 Pax1 paired box 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:23377878 11058 Pax1 paired box 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20200123 MGI PMID:24538930 11058 Pax1 paired box 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:23377878 11058 Pax1 paired box 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0000592 short tail IAGP N RGD:5509061 20200123 MGI PMID:24538930 11058 Pax1 paired box 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16315099 11058 Pax1 paired box 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23377878 11058 Pax1 paired box 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:16315099 11058 Pax1 paired box 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:19378260 11058 Pax1 paired box 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20200123 MGI PMID:24538930 11058 Pax1 paired box 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10656775 11058 Pax1 paired box 1 gene MP:0002116 abnormal craniofacial bone morphology IEA N RGD:5509061 20111116 MGI 11058 Pax1 paired box 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16315099 11058 Pax1 paired box 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19633672 11058 Pax1 paired box 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23377878 11058 Pax1 paired box 1 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20200123 MGI PMID:24538930 11058 Pax1 paired box 1 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:7550316 11058 Pax1 paired box 1 gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:7550316 11058 Pax1 paired box 1 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10656775 11058 Pax1 paired box 1 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7875377 11058 Pax1 paired box 1 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10656775 11058 Pax1 paired box 1 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19378260 11058 Pax1 paired box 1 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7875377 11058 Pax1 paired box 1 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:16315099 11058 Pax1 paired box 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:16315099 11058 Pax1 paired box 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:16315099 11058 Pax1 paired box 1 gene MP:0004083 polysyndactyly IEA N RGD:5509061 20111116 MGI 11058 Pax1 paired box 1 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0004346 absent acromion IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0004346 absent acromion IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0004346 absent acromion IAGP N RGD:5509061 20200123 MGI PMID:24538930 11058 Pax1 paired box 1 gene MP:0004347 abnormal scapular spine morphology IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0004604 abnormal vertebral pedicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0004604 abnormal vertebral pedicle morphology IAGP N RGD:5509061 20141003 MGI PMID:7875377 11058 Pax1 paired box 1 gene MP:0004605 abnormal vertebral lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:19378260 11058 Pax1 paired box 1 gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0004626 vertebral compression IAGP N RGD:5509061 20141003 MGI PMID:19378260 11058 Pax1 paired box 1 gene MP:0004626 vertebral compression IAGP N RGD:5509061 20141003 MGI PMID:7875377 11058 Pax1 paired box 1 gene MP:0004652 small caudal vertebrae IAGP N RGD:5509061 20200123 MGI PMID:24538930 11058 Pax1 paired box 1 gene MP:0004658 abnormal ventral tubercle of atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0004658 abnormal ventral tubercle of atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0004667 vertebral body hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0004668 absent vertebral body IAGP N RGD:5509061 20141003 MGI PMID:7875377 11058 Pax1 paired box 1 gene MP:0004668 absent vertebral body IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0004668 absent vertebral body IAGP N RGD:5509061 20150528 MGI PMID:8187635 11058 Pax1 paired box 1 gene MP:0004670 small vertebral body IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:7875377 11058 Pax1 paired box 1 gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20150528 MGI PMID:8187635 11058 Pax1 paired box 1 gene MP:0004687 split vertebrae IAGP N RGD:5509061 20141003 MGI PMID:7875377 11058 Pax1 paired box 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:7875377 11058 Pax1 paired box 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0005226 abnormal vertebral arch development IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0005229 abnormal intervertebral disk development IEA N RGD:5509061 20111116 MGI 11058 Pax1 paired box 1 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:7550316 11058 Pax1 paired box 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0006295 absent sclerotome IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0008149 abnormal costovertebral joint morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0008149 abnormal costovertebral joint morphology IAGP N RGD:5509061 20141003 MGI PMID:7875377 11058 Pax1 paired box 1 gene MP:0008149 abnormal costovertebral joint morphology IAGP N RGD:5509061 20150528 MGI PMID:8187635 11058 Pax1 paired box 1 gene MP:0009037 abnormal subarachnoid space development IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0009929 meningomyelocele IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0010701 fusion of atlas and odontoid process IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0010701 fusion of atlas and odontoid process IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0010701 fusion of atlas and odontoid process IAGP N RGD:5509061 20141003 MGI PMID:9671740 11058 Pax1 paired box 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16315099 11058 Pax1 paired box 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10364424 11058 Pax1 paired box 1 gene MP:0011400 lethality, complete penetrance IEA N RGD:5509061 20150528 MGI 11058 Pax1 paired box 1 gene MP:0013176 abnormal tail position or orientation IAGP N RGD:5509061 20141003 MGI PMID:16093716 11058 Pax1 paired box 1 gene MP:0013179 wavy tail IEA N RGD:5509061 20150528 MGI 11058 Pax1 paired box 1 gene MP:0030833 small acromion IAGP N RGD:5509061 20181018 MGI PMID:10656775 11058 Pax1 paired box 1 gene MP:0030833 small acromion IAGP N RGD:5509061 20200123 MGI PMID:24538930 11059 Pax6 paired box 6 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0000111 cleft palate IEA N RGD:5509061 20210826 MGI 11059 Pax6 paired box 6 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:11779807 11059 Pax6 paired box 6 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:1684639 11059 Pax6 paired box 6 gene MP:0000450 absent snout IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 11059 Pax6 paired box 6 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 11059 Pax6 paired box 6 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:19474196 11059 Pax6 paired box 6 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9232602 11059 Pax6 paired box 6 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19474196 11059 Pax6 paired box 6 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15548580 11059 Pax6 paired box 6 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 11059 Pax6 paired box 6 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:19500363 11059 Pax6 paired box 6 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 11059 Pax6 paired box 6 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16979618 11059 Pax6 paired box 6 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20141003 MGI PMID:15917450 11059 Pax6 paired box 6 gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 11059 Pax6 paired box 6 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 11059 Pax6 paired box 6 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 11059 Pax6 paired box 6 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:16289327 11059 Pax6 paired box 6 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:16289327 11059 Pax6 paired box 6 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16289327 11059 Pax6 paired box 6 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:16289327 11059 Pax6 paired box 6 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:17942732 11059 Pax6 paired box 6 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:15548580 11059 Pax6 paired box 6 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:19500363 11059 Pax6 paired box 6 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:23515312 11059 Pax6 paired box 6 gene MP:0001258 decreased body length IEA N RGD:5509061 20111116 MGI 11059 Pax6 paired box 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:11076764 11059 Pax6 paired box 6 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:23515312 11059 Pax6 paired box 6 gene MP:0001288 abnormal lens induction IAGP N RGD:5509061 20141003 MGI PMID:9851982 11059 Pax6 paired box 6 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:11481423 11059 Pax6 paired box 6 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:11714668 11059 Pax6 paired box 6 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:12714618 11059 Pax6 paired box 6 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:17064680 11059 Pax6 paired box 6 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:7035547 11059 Pax6 paired box 6 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:7789273 11059 Pax6 paired box 6 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:9166583 11059 Pax6 paired box 6 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:11062307 11059 Pax6 paired box 6 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:11779807 11059 Pax6 paired box 6 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:1684639 11059 Pax6 paired box 6 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:23592925 11059 Pax6 paired box 6 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:7035547 11059 Pax6 paired box 6 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:7649798 11059 Pax6 paired box 6 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:9163426 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10886015 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11062307 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11481423 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11779807 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11929848 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:12714618 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:16303964 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:1684639 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19474196 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19570848 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:20538882 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:22240097 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:23592925 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:9166583 11059 Pax6 paired box 6 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:11481423 11059 Pax6 paired box 6 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:11714668 11059 Pax6 paired box 6 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:11983873 11059 Pax6 paired box 6 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:17140559 11059 Pax6 paired box 6 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:19570848 11059 Pax6 paired box 6 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:22240097 11059 Pax6 paired box 6 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:9166583 11059 Pax6 paired box 6 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:10886015 11059 Pax6 paired box 6 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:11779807 11059 Pax6 paired box 6 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:16303964 11059 Pax6 paired box 6 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:19570848 11059 Pax6 paired box 6 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:7035547 11059 Pax6 paired box 6 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:19570848 11059 Pax6 paired box 6 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:20538882 11059 Pax6 paired box 6 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:23592925 11059 Pax6 paired box 6 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20141003 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20141003 MGI PMID:11929848 11059 Pax6 paired box 6 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20141003 MGI PMID:16303964 11059 Pax6 paired box 6 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20141003 MGI PMID:19474196 11059 Pax6 paired box 6 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20141003 MGI PMID:20538882 11059 Pax6 paired box 6 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20141003 MGI PMID:7035547 11059 Pax6 paired box 6 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20141003 MGI PMID:9166583 11059 Pax6 paired box 6 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20160310 MGI PMID:6877261 11059 Pax6 paired box 6 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:12714618 11059 Pax6 paired box 6 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:17064680 11059 Pax6 paired box 6 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:9166583 11059 Pax6 paired box 6 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:11062307 11059 Pax6 paired box 6 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:16303964 11059 Pax6 paired box 6 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:19474196 11059 Pax6 paired box 6 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:6877261 11059 Pax6 paired box 6 gene MP:0001317 abnormal pupil morphology IAGP N RGD:5509061 20141003 MGI PMID:11779807 11059 Pax6 paired box 6 gene MP:0001317 abnormal pupil morphology IAGP N RGD:5509061 20141003 MGI PMID:11983873 11059 Pax6 paired box 6 gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20141003 MGI PMID:11779807 11059 Pax6 paired box 6 gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:11062307 11059 Pax6 paired box 6 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:11779807 11059 Pax6 paired box 6 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:11983873 11059 Pax6 paired box 6 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11983873 11059 Pax6 paired box 6 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:4972360 11059 Pax6 paired box 6 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20538882 11059 Pax6 paired box 6 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7649798 11059 Pax6 paired box 6 gene MP:0001346 abnormal lacrimal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:22240097 11059 Pax6 paired box 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 11059 Pax6 paired box 6 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15110714 11059 Pax6 paired box 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210520 MGI 11059 Pax6 paired box 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15110714 11059 Pax6 paired box 6 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:19034419 11059 Pax6 paired box 6 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:7649798 11059 Pax6 paired box 6 gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:23592925 11059 Pax6 paired box 6 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17660683 11059 Pax6 paired box 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17660683 11059 Pax6 paired box 6 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11929848 11059 Pax6 paired box 6 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:19500363 11059 Pax6 paired box 6 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:23592925 11059 Pax6 paired box 6 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9363853 11059 Pax6 paired box 6 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 11059 Pax6 paired box 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19500363 11059 Pax6 paired box 6 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 11059 Pax6 paired box 6 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:9232602 11059 Pax6 paired box 6 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:16525473 11059 Pax6 paired box 6 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:7649798 11059 Pax6 paired box 6 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:1684639 11059 Pax6 paired box 6 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17660683 11059 Pax6 paired box 6 gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:11983873 11059 Pax6 paired box 6 gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:15110714 11059 Pax6 paired box 6 gene MP:0002697 abnormal eye size IAGP N RGD:5509061 20141003 MGI PMID:23592925 11059 Pax6 paired box 6 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:9166583 11059 Pax6 paired box 6 gene MP:0002700 increased opacity of vitreous body IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15110714 11059 Pax6 paired box 6 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11481423 11059 Pax6 paired box 6 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11714668 11059 Pax6 paired box 6 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19570848 11059 Pax6 paired box 6 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22240097 11059 Pax6 paired box 6 gene MP:0002938 white spotting IEA N RGD:5509061 20111116 MGI 11059 Pax6 paired box 6 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0003093 abnormal cornea anterior stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:12714618 11059 Pax6 paired box 6 gene MP:0003115 abnormal respiratory system development IAGP N RGD:5509061 20141003 MGI PMID:7789273 11059 Pax6 paired box 6 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210826 MGI 11059 Pax6 paired box 6 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:15548580 11059 Pax6 paired box 6 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11714668 11059 Pax6 paired box 6 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11983873 11059 Pax6 paired box 6 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19570848 11059 Pax6 paired box 6 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:4972360 11059 Pax6 paired box 6 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:15110714 11059 Pax6 paired box 6 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:11069887 11059 Pax6 paired box 6 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:7789273 11059 Pax6 paired box 6 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:9232602 11059 Pax6 paired box 6 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:9163426 11059 Pax6 paired box 6 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:14762144 11059 Pax6 paired box 6 gene MP:0003687 abnormal intraocular muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:4972360 11059 Pax6 paired box 6 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:19500363 11059 Pax6 paired box 6 gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11731698 11059 Pax6 paired box 6 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:11779807 11059 Pax6 paired box 6 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:19034419 11059 Pax6 paired box 6 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:9224716 11059 Pax6 paired box 6 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16289327 11059 Pax6 paired box 6 gene MP:0004171 abnormal pallium development IAGP N RGD:5509061 20141003 MGI PMID:11124115 11059 Pax6 paired box 6 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:17064680 11059 Pax6 paired box 6 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:20538882 11059 Pax6 paired box 6 gene MP:0004224 absent trabecular meshwork IAGP N RGD:5509061 20141003 MGI PMID:20538882 11059 Pax6 paired box 6 gene MP:0004226 absent Schlemm's canal IAGP N RGD:5509061 20141003 MGI PMID:20538882 11059 Pax6 paired box 6 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:11069887 11059 Pax6 paired box 6 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:1684639 11059 Pax6 paired box 6 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15548580 11059 Pax6 paired box 6 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 11059 Pax6 paired box 6 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:19474196 11059 Pax6 paired box 6 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:9363853 11059 Pax6 paired box 6 gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20141003 MGI PMID:17660683 11059 Pax6 paired box 6 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:16525473 11059 Pax6 paired box 6 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:23515312 11059 Pax6 paired box 6 gene MP:0004979 abnormal neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:23643363 11059 Pax6 paired box 6 gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:10451227 11059 Pax6 paired box 6 gene MP:0005128 decreased adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:19034419 11059 Pax6 paired box 6 gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:11481423 11059 Pax6 paired box 6 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:4972360 11059 Pax6 paired box 6 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20190808 MGI PMID:22792072 11059 Pax6 paired box 6 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:11481423 11059 Pax6 paired box 6 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:12714618 11059 Pax6 paired box 6 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:9166583 11059 Pax6 paired box 6 gene MP:0005208 abnormal iris stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:20538882 11059 Pax6 paired box 6 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11074448 11059 Pax6 paired box 6 gene MP:0005241 abnormal retina ganglion layer morphology IEA N RGD:5509061 20111116 MGI 11059 Pax6 paired box 6 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20141003 MGI PMID:20538882 11059 Pax6 paired box 6 gene MP:0005261 aniridia IAGP N RGD:5509061 20141003 MGI PMID:11983873 11059 Pax6 paired box 6 gene MP:0005261 aniridia IAGP N RGD:5509061 20141003 MGI PMID:2173141 11059 Pax6 paired box 6 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:22240097 11059 Pax6 paired box 6 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:9166583 11059 Pax6 paired box 6 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19034419 11059 Pax6 paired box 6 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:11983873 11059 Pax6 paired box 6 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:12692153 11059 Pax6 paired box 6 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:12714618 11059 Pax6 paired box 6 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:20538882 11059 Pax6 paired box 6 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:9166583 11059 Pax6 paired box 6 gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17064680 11059 Pax6 paired box 6 gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9166583 11059 Pax6 paired box 6 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:12714618 11059 Pax6 paired box 6 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:17051153 11059 Pax6 paired box 6 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:17064680 11059 Pax6 paired box 6 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:11076764 11059 Pax6 paired box 6 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:11481423 11059 Pax6 paired box 6 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:19570848 11059 Pax6 paired box 6 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12692153 11059 Pax6 paired box 6 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:4972360 11059 Pax6 paired box 6 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0006095 absent amacrine cells IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 11059 Pax6 paired box 6 gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20141003 MGI PMID:20538882 11059 Pax6 paired box 6 gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20538882 11059 Pax6 paired box 6 gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11983873 11059 Pax6 paired box 6 gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12714618 11059 Pax6 paired box 6 gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16979618 11059 Pax6 paired box 6 gene MP:0006293 absent nasal placodes IAGP N RGD:5509061 20141003 MGI PMID:7789273 11059 Pax6 paired box 6 gene MP:0006369 supernumerary incisors IAGP N RGD:5509061 20141003 MGI PMID:9363853 11059 Pax6 paired box 6 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:19500363 11059 Pax6 paired box 6 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:23515312 11059 Pax6 paired box 6 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20141003 MGI PMID:15548580 11059 Pax6 paired box 6 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20141003 MGI PMID:23515312 11059 Pax6 paired box 6 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:19474196 11059 Pax6 paired box 6 gene MP:0008521 abnormal Bowman membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12714618 11059 Pax6 paired box 6 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23643363 11059 Pax6 paired box 6 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11074448 11059 Pax6 paired box 6 gene MP:0008794 increased lens epithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19570848 11059 Pax6 paired box 6 gene MP:0008797 facial cleft IEA N RGD:5509061 20210520 MGI 11059 Pax6 paired box 6 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:15917450 11059 Pax6 paired box 6 gene MP:0008946 abnormal neuron number IAGP N RGD:5509061 20141003 MGI PMID:23643363 11059 Pax6 paired box 6 gene MP:0009174 absent pancreatic beta cells IAGP N RGD:5509061 20141003 MGI PMID:9224716 11059 Pax6 paired box 6 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:15110714 11059 Pax6 paired box 6 gene MP:0009178 absent pancreatic alpha cells IAGP N RGD:5509061 20141003 MGI PMID:9163426 11059 Pax6 paired box 6 gene MP:0009178 absent pancreatic alpha cells IAGP N RGD:5509061 20141003 MGI PMID:9224716 11059 Pax6 paired box 6 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:9163426 11059 Pax6 paired box 6 gene MP:0009265 delayed eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:11481423 11059 Pax6 paired box 6 gene MP:0009522 submandibular gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11731698 11059 Pax6 paired box 6 gene MP:0009637 abnormal pretectal region morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 11059 Pax6 paired box 6 gene MP:0009703 decreased birth body size IEA N RGD:5509061 20111116 MGI 11059 Pax6 paired box 6 gene MP:0009725 absent lens vesicle IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0009725 absent lens vesicle IAGP N RGD:5509061 20141003 MGI PMID:7789273 11059 Pax6 paired box 6 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:23515312 11059 Pax6 paired box 6 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0009859 eye opacity IAGP N RGD:5509061 20141003 MGI PMID:19474196 11059 Pax6 paired box 6 gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:11779807 11059 Pax6 paired box 6 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:11779807 11059 Pax6 paired box 6 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15548580 11059 Pax6 paired box 6 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16950124 11059 Pax6 paired box 6 gene MP:0010259 anterior polar cataract IAGP N RGD:5509061 20141003 MGI PMID:10886015 11059 Pax6 paired box 6 gene MP:0010259 anterior polar cataract IAGP N RGD:5509061 20141003 MGI PMID:11779807 11059 Pax6 paired box 6 gene MP:0010259 anterior polar cataract IAGP N RGD:5509061 20141003 MGI PMID:6877261 11059 Pax6 paired box 6 gene MP:0010259 anterior polar cataract IAGP N RGD:5509061 20141003 MGI PMID:9166583 11059 Pax6 paired box 6 gene MP:0010292 increased alimentary system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17660683 11059 Pax6 paired box 6 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17660683 11059 Pax6 paired box 6 gene MP:0010709 absent eye anterior chamber IAGP N RGD:5509061 20201119 MGI PMID:20538882 11059 Pax6 paired box 6 gene MP:0010713 corneal-lenticular stalk IAGP N RGD:5509061 20141003 MGI PMID:16303964 11059 Pax6 paired box 6 gene MP:0010713 corneal-lenticular stalk IAGP N RGD:5509061 20141003 MGI PMID:22240097 11059 Pax6 paired box 6 gene MP:0010713 corneal-lenticular stalk IAGP N RGD:5509061 20141003 MGI PMID:23515312 11059 Pax6 paired box 6 gene MP:0010713 corneal-lenticular stalk IAGP N RGD:5509061 20141003 MGI PMID:23592925 11059 Pax6 paired box 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11779807 11059 Pax6 paired box 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15110714 11059 Pax6 paired box 6 gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 11059 Pax6 paired box 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10451227 11059 Pax6 paired box 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1684639 11059 Pax6 paired box 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9163426 11059 Pax6 paired box 6 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23592925 11059 Pax6 paired box 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7649798 11059 Pax6 paired box 6 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11062307 11059 Pax6 paired box 6 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 11059 Pax6 paired box 6 gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 11059 Pax6 paired box 6 gene MP:0011102 embryonic lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 11059 Pax6 paired box 6 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IEA N RGD:5509061 20111116 MGI 11059 Pax6 paired box 6 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141003 MGI PMID:10886015 11059 Pax6 paired box 6 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141003 MGI PMID:11779807 11059 Pax6 paired box 6 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141003 MGI PMID:12714618 11059 Pax6 paired box 6 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141003 MGI PMID:17064680 11059 Pax6 paired box 6 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141003 MGI PMID:20538882 11059 Pax6 paired box 6 gene MP:0011932 abnormal endocrine pancreas development IAGP N RGD:5509061 20141003 MGI PMID:18199433 11059 Pax6 paired box 6 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20230810 MGI PMID:19570848 11059 Pax6 paired box 6 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0012168 abnormal optic placode morphology IAGP N RGD:5509061 20141003 MGI PMID:11714668 11059 Pax6 paired box 6 gene MP:0012168 abnormal optic placode morphology IAGP N RGD:5509061 20141003 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0012170 absent optic placodes IAGP N RGD:5509061 20141003 MGI PMID:11069887 11059 Pax6 paired box 6 gene MP:0012517 absent diencephalon IAGP N RGD:5509061 20141003 MGI PMID:15917450 11059 Pax6 paired box 6 gene MP:0013742 absent ciliary body IAGP N RGD:5509061 20150416 MGI PMID:19563798 11059 Pax6 paired box 6 gene MP:0013791 absent external nares IAGP N RGD:5509061 20150611 MGI PMID:11062307 11059 Pax6 paired box 6 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:15917450 11059 Pax6 paired box 6 gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:12692153 11059 Pax6 paired box 6 gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:12714618 11059 Pax6 paired box 6 gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:17051153 11059 Pax6 paired box 6 gene MP:0021101 abnormal ventral interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:16525473 11059 Pax6 paired box 6 gene MP:0021102 abnormal ventral interneuron 0 morphology IAGP N RGD:5509061 20220310 MGI PMID:16525473 11059 Pax6 paired box 6 gene MP:0021103 abnormal ventral interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:14762144 11059 Pax6 paired box 6 gene MP:0021103 abnormal ventral interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:16525473 11059 Pax6 paired box 6 gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:16525473 11059 Pax6 paired box 6 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:103464 11059 Pax6 paired box 6 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:24523460 11059 Pax6 paired box 6 gene MP:0030060 absent nasal pit IAGP N RGD:5509061 20170921 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20171109 MGI PMID:3794606 11059 Pax6 paired box 6 gene MP:0031345 developmental cataract IEA N RGD:5509061 20220217 MGI 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:10938127 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16300682 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:10938127 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:10938127 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10938127 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10938127 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16300682 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:10938127 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:11792850 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:16300682 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11792850 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10938127 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:16300682 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16300682 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11792850 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:10938127 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:11792850 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:10938127 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:16300682 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:10938127 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:16300682 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:16300682 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:16300682 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16300682 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16300682 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:11792850 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11792850 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11792850 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11792850 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0009122 decreased white fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:11792850 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0009128 decreased brown fat cell number IAGP N RGD:5509061 20141003 MGI PMID:11792850 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:11792850 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20141003 MGI PMID:11792850 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11792850 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10938127 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11792850 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:10938127 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:10938127 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:16300682 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10938127 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16300682 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20141003 MGI PMID:11792850 11062 Pck1 phosphoenolpyruvate carboxykinase 1, cytosolic gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:16300682 11062069 Bpq31_m blood pressure QTL 31 (mouse) qtl MP:0000231 hypertension IAGP N RGD:5509061 20160428 MGI PMID:12118100 11062069 Bpq31_m blood pressure QTL 31 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20160422 MGI Created by mouse qtl pipeline PMID:12118100 11062078 Axtofd7_m anxiety-open field defecation 7 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160422 MGI Created by mouse qtl pipeline PMID:11454769 11062079 Axtofd6_m anxiety-open field defecation 6 (mouse) qtl MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20160428 MGI PMID:14990867 11062079 Axtofd6_m anxiety-open field defecation 6 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160422 MGI Created by mouse qtl pipeline PMID:11454769 11062080 Axtofa10_m anxiety-open field activity 10 (mouse) qtl MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160428 MGI PMID:14990867 11062080 Axtofa10_m anxiety-open field activity 10 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160422 MGI Created by mouse qtl pipeline PMID:11454769 11062081 Axtofa9_m anxiety-open field activity 9 (mouse) qtl MP:0001399 hyperactivity IAGP N RGD:5509061 20160428 MGI PMID:14990867 11062081 Axtofa9_m anxiety-open field activity 9 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160422 MGI Created by mouse qtl pipeline PMID:11418486|PMID:11454769 11062082 Axtofa8_m anxiety-open field activity 8 (mouse) qtl MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160428 MGI PMID:14990867 11062082 Axtofa8_m anxiety-open field activity 8 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160422 MGI Created by mouse qtl pipeline PMID:11454769 11063 Pcp4 Purkinje cell protein 4 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20180215 MGI PMID:28069794 11063 Pcp4 Purkinje cell protein 4 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:21576365 11063 Pcp4 Purkinje cell protein 4 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:21576365 11063 Pcp4 Purkinje cell protein 4 gene MP:0005238 increased brain size IAGP N RGD:5509061 20180215 MGI PMID:28069794 11063 Pcp4 Purkinje cell protein 4 gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20180215 MGI PMID:28069794 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20141003 MGI 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20150903 MGI PMID:26272049 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20150903 MGI PMID:26272049 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20150903 MGI PMID:26272049 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20150903 MGI PMID:26272049 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20150903 MGI PMID:26272049 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20150903 MGI PMID:26272049 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20150903 MGI PMID:26272049 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0002923 increased post-tetanic potentiation IAGP N RGD:5509061 20150903 MGI PMID:26272049 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20150903 MGI PMID:26272049 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0008025 brain vacuoles IEA N RGD:5509061 20141003 MGI 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:12032334 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16034090 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:15585880 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15585880 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20150903 MGI PMID:26272049 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16034090 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20150903 MGI PMID:26272049 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15585880 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0012314 enhanced learning IAGP N RGD:5509061 20150903 MGI PMID:26272049 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0014369 enhanced spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:26272049 11065 Pde4b phosphodiesterase 4B, cAMP specific gene MP:0020507 increased dendritic spine density IAGP N RGD:5509061 20211014 MGI PMID:26272049 11066 Pde4d phosphodiesterase 4D, cAMP specific gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10518565 11066 Pde4d phosphodiesterase 4D, cAMP specific gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10518565 11066 Pde4d phosphodiesterase 4D, cAMP specific gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10518565 11066 Pde4d phosphodiesterase 4D, cAMP specific gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10518565 11066 Pde4d phosphodiesterase 4D, cAMP specific gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15644445 11066 Pde4d phosphodiesterase 4D, cAMP specific gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:15585880 11066 Pde4d phosphodiesterase 4D, cAMP specific gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15585880 11066 Pde4d phosphodiesterase 4D, cAMP specific gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15585880 11066 Pde4d phosphodiesterase 4D, cAMP specific gene MP:0009777 abnormal behavioral response to anesthetic IAGP N RGD:5509061 20210513 MGI PMID:33609559 11066 Pde4d phosphodiesterase 4D, cAMP specific gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10518565 11066 Pde4d phosphodiesterase 4D, cAMP specific gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15585880 11066 Pde4d phosphodiesterase 4D, cAMP specific gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:10518565 11067 Pdgfa platelet derived growth factor, alpha gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:23938297 11067 Pdgfa platelet derived growth factor, alpha gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:23938297 11067 Pdgfa platelet derived growth factor, alpha gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:14522834 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:14522834 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:23938297 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001184 absent pulmonary alveoli IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23938297 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:14522834 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:23938297 11067 Pdgfa platelet derived growth factor, alpha gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:23938297 11067 Pdgfa platelet derived growth factor, alpha gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:14522834 11067 Pdgfa platelet derived growth factor, alpha gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:23938297 11067 Pdgfa platelet derived growth factor, alpha gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0004735 enlarged thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14522834 11067 Pdgfa platelet derived growth factor, alpha gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:23938297 11067 Pdgfa platelet derived growth factor, alpha gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0010822 pneumothorax IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0010901 abnormal pulmonary alveolar parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14522834 11067 Pdgfa platelet derived growth factor, alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15361870 11067 Pdgfa platelet derived growth factor, alpha gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8681381 11067 Pdgfa platelet derived growth factor, alpha gene MP:0014079 decreased small intestinal villus number IAGP N RGD:5509061 20160414 MGI PMID:23938297 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15084468 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:12169633 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11331305 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20944627 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20200910 MGI PMID:15084468 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20944627 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:15084468 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:15084468 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12169633 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:15084468 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:10419690 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:15084468 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11331305 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:11331305 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:15084468 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:20944627 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10419690 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12169633 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15084468 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20944627 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10419690 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0005096 erythroblastosis IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:15084468 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11331305 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:11331305 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12169633 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0006186 retina fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10419690 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0010451 kidney microaneurysm IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0010479 brain aneurysm IAGP N RGD:5509061 20141003 MGI PMID:15084468 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0010574 dilated aorta IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0011428 decreased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0011428 decreased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:15084468 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0011428 decreased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0011429 absent mesangial cell IAGP N RGD:5509061 20141003 MGI PMID:7958863 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0011509 dilated glomerular capillary IAGP N RGD:5509061 20141003 MGI PMID:12897053 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0011509 dilated glomerular capillary IAGP N RGD:5509061 20141003 MGI PMID:15084468 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0020329 decreased capillary density IAGP N RGD:5509061 20160714 MGI PMID:15084468 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0020329 decreased capillary density IAGP N RGD:5509061 20160714 MGI PMID:20944627 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0020331 increased capillary tortuosity IAGP N RGD:5509061 20160714 MGI PMID:15084468 11068 Pdgfb platelet derived growth factor, B polypeptide gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:20944627 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000091 short premaxilla IAGP N RGD:5509061 20141003 MGI PMID:17143286 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:17143286 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12490557 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000105 impaired ossification of basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12490557 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:12490557 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:17143286 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17143286 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17499702 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000158 absent sternum IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:12490557 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000445 short snout IAGP N RGD:5509061 20171019 MGI PMID:17143286 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:17499702 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12490557 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000924 absent roof plate IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:23938297 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17568391 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20231109 MGI PMID:20071345 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21576357 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21576357 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17499702 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17143286 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23335233 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:12490557 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001699 increased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17499702 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12490557 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:23938297 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12490557 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:21576357 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11239463 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:23938297 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:12490557 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:17499702 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002683 delayed fertility IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0002990 short ureter IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:17003488 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20231109 MGI PMID:20071345 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003586 dilated ureter IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003587 ureter obstruction IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:23335233 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:17568391 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003939 abnormal myotome morphology IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:17499702 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0004199 increased fetal size IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0004202 pulmonary hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0004260 enlarged placenta IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:17143286 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0004506 abnormal pubis morphology IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0004508 abnormal pectoral girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0004546 esophagus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:21576357 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:12490557 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21576357 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0006418 abnormal testis cord formation IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:21576357 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0008856 fetal bleb IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0008856 fetal bleb IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0009370 decreased theca cell number IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:12490557 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17499702 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17568391 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12490557 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0010440 anomalous pulmonary venous connection IAGP N RGD:5509061 20231109 MGI PMID:20071345 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0010441 total anomalous pulmonary venous connection IAGP N RGD:5509061 20231109 MGI PMID:20071345 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0010528 pulmonary vein hypoplasia IAGP N RGD:5509061 20231109 MGI PMID:20071345 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0010548 abnormal dorsal mesocardium morphology IAGP N RGD:5509061 20231109 MGI PMID:20071345 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0010901 abnormal pulmonary alveolar parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:17003488 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11782318 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17499702 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23335233 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17568391 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:20071345 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011147 increased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011180 abnormal hematopoietic cell number IAGP N RGD:5509061 20141003 MGI PMID:23335233 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011185 absent primitive endoderm IAGP N RGD:5509061 20160728 MGI PMID:24835466 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20141003 MGI PMID:19056881 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011426 abnormal ureter smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011683 dual inferior vena cava IAGP N RGD:5509061 20231109 MGI PMID:20071345 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20170223 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0011748 intestinal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:17499702 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20141003 MGI PMID:17568391 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0012279 wide sternum IAGP N RGD:5509061 20141003 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:17499702 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0012754 abnormal cranial neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0014166 ectopic cranial bone IAGP N RGD:5509061 20160407 MGI PMID:12748302 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0020417 increased fibroblast chemotaxis IAGP N RGD:5509061 20170223 MGI PMID:19217431 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:17143286 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0030189 broad snout IAGP N RGD:5509061 20171019 MGI PMID:17143286 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0030834 acromion hypoplasia IAGP N RGD:5509061 20181018 MGI PMID:9226440 11069 Pdgfra platelet derived growth factor receptor, alpha polypeptide gene MP:0031138 testicular hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:19056881 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:11782318 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17499702 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:11782318 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16690964 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20150326 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20150326 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000314 schistocytosis IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15590688 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000445 short snout IEA N RGD:5509061 20150326 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000484 abnormal pulmonary artery morphology IEA N RGD:5509061 20150326 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:17499702 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000767 abnormal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11782318 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19056881 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160915 MGI PMID:25803852 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210826 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17499702 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11331305 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11782318 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:15590688 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17499702 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19056881 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19056881 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20160811 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:11124809 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:17143286 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20160915 MGI PMID:25803852 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:17499702 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002635 reduced sensorimotor gating IAGP N RGD:5509061 20160915 MGI PMID:25803852 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002639 micrognathia IEA N RGD:5509061 20150326 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:16037818 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:19056881 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20151001 MGI PMID:23633653 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20151001 MGI PMID:23633653 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003099 retina detachment IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:10419690 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16690964 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10419690 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20151001 MGI PMID:23633653 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11782318 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0004125 abnormal venule morphology IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0004158 right aortic arch IEA N RGD:5509061 20150326 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:17499702 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20151001 MGI PMID:23633653 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10419690 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:16805849 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0005327 abnormal mesangial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11124809 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0005327 abnormal mesangial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0005489 vascular smooth muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17143286 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16690964 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15590688 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11331305 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:11331305 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0006185 retina hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0006203 eye hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0006203 eye hemorrhage IAGP N RGD:5509061 20151001 MGI PMID:23633653 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0006253 clinodactyly IEA N RGD:5509061 20150326 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20151001 MGI PMID:23633653 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20151001 MGI PMID:23633653 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0008137 absent podocytes IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:16805849 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10419690 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0008816 petechiae IEA N RGD:5509061 20150326 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0008856 fetal bleb IAGP N RGD:5509061 20141003 MGI PMID:11782318 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0008903 abnormal mesenteric fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20160915 MGI PMID:25803852 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0009130 increased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20160915 MGI PMID:25803852 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:11782318 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0009859 eye opacity IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0009869 abnormal descending aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0009870 abnormal abdominal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20151001 MGI PMID:23633653 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20151001 MGI PMID:23633653 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17499702 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20150326 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17499702 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20150326 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0010451 kidney microaneurysm IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0010466 vascular ring IEA N RGD:5509061 20150326 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0010468 abnormal thoracic aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0010488 abnormal left subclavian artery morphology IEA N RGD:5509061 20150326 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0010574 dilated aorta IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17499702 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19056881 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011156 abnormal hypodermis fat layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011169 abnormal white fat cell differentation IAGP N RGD:5509061 20141003 MGI PMID:21664579 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011359 decreased glomerular capillary number IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011429 absent mesangial cell IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011437 glomerulus hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11124809 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011508 abnormal glomerular capillary thrombosis IAGP N RGD:5509061 20141003 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011514 skin hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14624252 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011515 purpura IAGP N RGD:5509061 20141003 MGI PMID:7958864 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:11124809 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0011706 abnormal fibroblast migration IAGP N RGD:5509061 20150212 MGI PMID:15284236 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:17499702 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:15284236 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0014179 abnormal blood-retina barrier function IAGP N RGD:5509061 20160526 MGI PMID:23633653 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:23633653 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:11239463 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0031138 testicular hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:19056881 11070 Pdgfrb platelet derived growth factor receptor, beta polypeptide gene MP:0031510 increased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:21664579 11074 Pepc peptidase C gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 11074 Pepc peptidase C gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20180329 MGI PMID:29440507 11074 Pepc peptidase C gene MP:0009785 abnormal susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20180329 MGI PMID:29440507 11074 Pepc peptidase C gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20180329 MGI PMID:29440507 11074 Pepc peptidase C gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:29440507 11074 Pepc peptidase C gene MP:0031045 decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:29440507 11075 Pepd peptidase D gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 11075 Pepd peptidase D gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20220519 MGI 11075 Pepd peptidase D gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 11075 Pepd peptidase D gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0000372 irregular coat pigmentation IEA N RGD:5509061 20141211 MGI 11075 Pepd peptidase D gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220811 MGI 11075 Pepd peptidase D gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141211 MGI PMID:18821597 11075 Pepd peptidase D gene MP:0001147 small testis IAGP N RGD:5509061 20141211 MGI PMID:18821597 11075 Pepd peptidase D gene MP:0001261 obese IAGP N RGD:5509061 20141218 MGI PMID:18821597 11075 Pepd peptidase D gene MP:0001265 decreased body size IAGP N RGD:5509061 20141218 MGI PMID:18821597 11075 Pepd peptidase D gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201231 MGI 11075 Pepd peptidase D gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 11075 Pepd peptidase D gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20240627 MGI 11075 Pepd peptidase D gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 11075 Pepd peptidase D gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 11075 Pepd peptidase D gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 11075 Pepd peptidase D gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141211 MGI PMID:18821597 11075 Pepd peptidase D gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 11075 Pepd peptidase D gene MP:0002691 small stomach IEA N RGD:5509061 20181227 MGI 11075 Pepd peptidase D gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20210128 MGI 11075 Pepd peptidase D gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 11075 Pepd peptidase D gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141211 MGI PMID:18821597 11075 Pepd peptidase D gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20210128 MGI 11075 Pepd peptidase D gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20181227 MGI 11075 Pepd peptidase D gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141218 MGI PMID:18821597 11075 Pepd peptidase D gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20181227 MGI 11075 Pepd peptidase D gene MP:0003808 increased atrioventricular cushion size IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20201022 MGI 11075 Pepd peptidase D gene MP:0004924 abnormal behavior IEA N RGD:5509061 20181227 MGI 11075 Pepd peptidase D gene MP:0005017 decreased B cell number IEA N RGD:5509061 20230601 MGI 11075 Pepd peptidase D gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 11075 Pepd peptidase D gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20201022 MGI 11075 Pepd peptidase D gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141211 MGI PMID:18821597 11075 Pepd peptidase D gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0005431 decreased oocyte number IEA N RGD:5509061 20141211 MGI 11075 Pepd peptidase D gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 11075 Pepd peptidase D gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141211 MGI PMID:18821597 11075 Pepd peptidase D gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 11075 Pepd peptidase D gene MP:0008174 decreased follicular B cell number IEA N RGD:5509061 20220811 MGI 11075 Pepd peptidase D gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20230601 MGI 11075 Pepd peptidase D gene MP:0008215 decreased immature B cell number IEA N RGD:5509061 20201231 MGI 11075 Pepd peptidase D gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20181227 MGI 11075 Pepd peptidase D gene MP:0009643 abnormal urine homeostasis IEA N RGD:5509061 20141211 MGI 11075 Pepd peptidase D gene MP:0009923 decreased transitional stage T1 B cell number IEA N RGD:5509061 20201231 MGI 11075 Pepd peptidase D gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 11075 Pepd peptidase D gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 11075 Pepd peptidase D gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0010770 preweaning lethality IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 11075 Pepd peptidase D gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0011416 abnormal testis interstitial tissue morphology IAGP N RGD:5509061 20141211 MGI PMID:18821597 11075 Pepd peptidase D gene MP:0011640 abnormal aorta collagen fibril morphology IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0011896 increased circulating unsaturated transferrin level IEA N RGD:5509061 20211021 MGI 11075 Pepd peptidase D gene MP:0012076 abnormal agouti pigmentation IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0013427 increased memory-marker NK cell number IEA N RGD:5509061 20201231 MGI 11075 Pepd peptidase D gene MP:0013430 increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 11075 Pepd peptidase D gene MP:0013514 increased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 11075 Pepd peptidase D gene MP:0013678 decreased Ly6C-positive NK T cell number IEA N RGD:5509061 20201231 MGI 11075 Pepd peptidase D gene MP:0013691 decreased CD5-positive Ly6C-positive T cell number IEA N RGD:5509061 20220811 MGI 11075 Pepd peptidase D gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20201231 MGI 11075 Pepd peptidase D gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20141211 MGI PMID:21472842 11075 Pepd peptidase D gene MP:0031609 increased fetal cardiomyocyte size IAGP N RGD:5509061 20240321 MGI PMID:21472842 11075102 Modc2_m modifier of Odc2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20160506 MGI Created by mouse qtl pipeline PMID:16086382 11075102 Modc2_m modifier of Odc2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20160506 MGI Created by mouse qtl pipeline PMID:16086382 11075105 Modc1_m modifier of Odc1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20160506 MGI Created by mouse qtl pipeline PMID:11944982 11082165 Cd300ld2 CD300 molecule like family member D2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 11082165 Cd300ld2 CD300 molecule like family member D2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 11082165 Cd300ld2 CD300 molecule like family member D2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20210128 MGI 11082165 Cd300ld2 CD300 molecule like family member D2 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20210128 MGI 11082585 4931422A03Rik RIKEN cDNA 4931422A03 gene gene MP:0001257 increased body length IEA N RGD:5509061 20211021 MGI 11082624 Prr35 proline rich 35 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20230720 MGI 11082624 Prr35 proline rich 35 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20230720 MGI 11085 Pfkfb2 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20160421 MGI 11085 Pfkfb2 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20201022 MGI 11085 Pfkfb2 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 11085 Pfkfb2 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 11085 Pfkfb2 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20201119 MGI PMID:32884050 11085 Pfkfb2 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20201119 MGI PMID:32884050 11085 Pfkfb2 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 11085 Pfkfb2 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20160421 MGI 11085 Pfkfb2 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20201119 MGI PMID:32884050 11085 Pfkfb2 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 11085 Pfkfb2 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 gene MP:0031003 increased kidney glycogen level IAGP N RGD:5509061 20201119 MGI PMID:32884050 11087 Pgd phosphogluconate dehydrogenase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0001265 decreased body size IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0001849 ear inflammation IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0002083 premature death IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20210909 MGI PMID:33691103 11087 Pgd phosphogluconate dehydrogenase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0002495 increased IgA level IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0002496 increased IgD level IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0002497 increased IgE level IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 11087 Pgd phosphogluconate dehydrogenase gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20210909 MGI PMID:33691103 11087 Pgd phosphogluconate dehydrogenase gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20210909 MGI PMID:33691103 11087 Pgd phosphogluconate dehydrogenase gene MP:0005015 increased T cell number IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20210909 MGI PMID:33691103 11087 Pgd phosphogluconate dehydrogenase gene MP:0005251 blepharitis IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0005440 increased glycogen level IAGP N RGD:5509061 20210909 MGI PMID:33691103 11087 Pgd phosphogluconate dehydrogenase gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20210909 MGI PMID:33691103 11087 Pgd phosphogluconate dehydrogenase gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20210909 MGI PMID:33691103 11087 Pgd phosphogluconate dehydrogenase gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0008626 increased circulating interleukin-5 level IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0010183 abnormal CD4-positive helper T cell morphology IAGP N RGD:5509061 20240627 MGI PMID:34709178 11087 Pgd phosphogluconate dehydrogenase gene MP:0012762 abnormal alpha-beta T cell morphology IAGP N RGD:5509061 20210909 MGI PMID:33691103 11091 Pgm1 phosphoglucomutase 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20210422 MGI 11091 Pgm1 phosphoglucomutase 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20210422 MGI 11091 Pgm1 phosphoglucomutase 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20210422 MGI 11091 Pgm1 phosphoglucomutase 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210422 MGI 11091 Pgm1 phosphoglucomutase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20230629 MGI PMID:31077402 11091 Pgm1 phosphoglucomutase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 11091 Pgm1 phosphoglucomutase 1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20230629 MGI PMID:31077402 11091 Pgm1 phosphoglucomutase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20230629 MGI PMID:31077402 11091 Pgm1 phosphoglucomutase 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210520 MGI 11092 Pgr progesterone receptor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18276762 11092 Pgr progesterone receptor gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:18276762 11092 Pgr progesterone receptor gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:21862609 11092 Pgr progesterone receptor gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:12403837 11092 Pgr progesterone receptor gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:7557380 11092 Pgr progesterone receptor gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:12897242 11092 Pgr progesterone receptor gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:17045797 11092 Pgr progesterone receptor gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:7557380 11092 Pgr progesterone receptor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12403837 11092 Pgr progesterone receptor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17941046 11092 Pgr progesterone receptor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:19439667 11092 Pgr progesterone receptor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:21209023 11092 Pgr progesterone receptor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:7557380 11092 Pgr progesterone receptor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20170622 MGI PMID:25043182 11092 Pgr progesterone receptor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20190215 MGI PMID:27018534 11092 Pgr progesterone receptor gene MP:0001123 dilated uterus IAGP N RGD:5509061 20141003 MGI PMID:7557380 11092 Pgr progesterone receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:12403837 11092 Pgr progesterone receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:7557380 11092 Pgr progesterone receptor gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:20418913 11092 Pgr progesterone receptor gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20150709 MGI PMID:23820898 11092 Pgr progesterone receptor gene MP:0001376 abnormal mating receptivity IAGP N RGD:5509061 20141003 MGI PMID:7557380 11092 Pgr progesterone receptor gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20220519 MGI PMID:35349646 11092 Pgr progesterone receptor gene MP:0001619 abnormal vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:24485460 11092 Pgr progesterone receptor gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20150709 MGI PMID:23820898 11092 Pgr progesterone receptor gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20170622 MGI PMID:25043182 11092 Pgr progesterone receptor gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20230302 MGI PMID:35194044 11092 Pgr progesterone receptor gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20170622 MGI PMID:25043182 11092 Pgr progesterone receptor gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20230302 MGI PMID:35194044 11092 Pgr progesterone receptor gene MP:0001727 abnormal embryo implantation IAGP N RGD:5509061 20220519 MGI PMID:35349646 11092 Pgr progesterone receptor gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:17045797 11092 Pgr progesterone receptor gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20190321 MGI PMID:30626716 11092 Pgr progesterone receptor gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20220303 MGI PMID:22233806 11092 Pgr progesterone receptor gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20220512 MGI PMID:27783953 11092 Pgr progesterone receptor gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20220602 MGI PMID:33590845 11092 Pgr progesterone receptor gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:24485460 11092 Pgr progesterone receptor gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20170622 MGI PMID:25043182 11092 Pgr progesterone receptor gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20220120 MGI PMID:31875883 11092 Pgr progesterone receptor gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20220203 MGI PMID:20484741 11092 Pgr progesterone receptor gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20220303 MGI PMID:22233806 11092 Pgr progesterone receptor gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20230302 MGI PMID:35194044 11092 Pgr progesterone receptor gene MP:0001881 abnormal mammary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:20029965 11092 Pgr progesterone receptor gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:12897242 11092 Pgr progesterone receptor gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:12403837 11092 Pgr progesterone receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20170622 MGI PMID:25043182 11092 Pgr progesterone receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20180315 MGI PMID:28005395 11092 Pgr progesterone receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20211209 MGI PMID:30954472 11092 Pgr progesterone receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220120 MGI PMID:31875883 11092 Pgr progesterone receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220203 MGI PMID:20484741 11092 Pgr progesterone receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220303 MGI PMID:22233806 11092 Pgr progesterone receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220519 MGI PMID:35349646 11092 Pgr progesterone receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220602 MGI PMID:33590845 11092 Pgr progesterone receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20230302 MGI PMID:35194044 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10976068 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12403837 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16868919 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17045797 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17941046 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19439667 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20382891 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:21209023 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:21508348 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:23079602 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:7557380 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20190215 MGI PMID:27018534 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20190321 MGI PMID:30626716 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20220303 MGI PMID:22233806 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20220512 MGI PMID:27783953 11092 Pgr progesterone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20220602 MGI PMID:33590845 11092 Pgr progesterone receptor gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20141003 MGI PMID:12403837 11092 Pgr progesterone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20170622 MGI PMID:25043182 11092 Pgr progesterone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20180315 MGI PMID:28005395 11092 Pgr progesterone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20211209 MGI PMID:30954472 11092 Pgr progesterone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220120 MGI PMID:31875883 11092 Pgr progesterone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220203 MGI PMID:20484741 11092 Pgr progesterone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220303 MGI PMID:22233806 11092 Pgr progesterone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220519 MGI PMID:35349646 11092 Pgr progesterone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220602 MGI PMID:33590845 11092 Pgr progesterone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20230302 MGI PMID:35194044 11092 Pgr progesterone receptor gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20160728 MGI PMID:25377472 11092 Pgr progesterone receptor gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:24474556 11092 Pgr progesterone receptor gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:14667968 11092 Pgr progesterone receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12438645 11092 Pgr progesterone receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18632614 11092 Pgr progesterone receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20418913 11092 Pgr progesterone receptor gene MP:0002083 premature death IAGP N RGD:5509061 20160728 MGI PMID:25377472 11092 Pgr progesterone receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12403837 11092 Pgr progesterone receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16868919 11092 Pgr progesterone receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23663785 11092 Pgr progesterone receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25377472 11092 Pgr progesterone receptor gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:12403837 11092 Pgr progesterone receptor gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:17941046 11092 Pgr progesterone receptor gene MP:0002676 uterus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10976068 11092 Pgr progesterone receptor gene MP:0002676 uterus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12403837 11092 Pgr progesterone receptor gene MP:0002676 uterus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7557380 11092 Pgr progesterone receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:10433223 11092 Pgr progesterone receptor gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20211209 MGI PMID:30954472 11092 Pgr progesterone receptor gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20220519 MGI PMID:35349646 11092 Pgr progesterone receptor gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:18026113 11092 Pgr progesterone receptor gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:12438645 11092 Pgr progesterone receptor gene MP:0003356 impaired luteinization IAGP N RGD:5509061 20141003 MGI PMID:7557380 11092 Pgr progesterone receptor gene MP:0003570 increased uterus leiomyoma incidence IAGP N RGD:5509061 20150709 MGI PMID:23820898 11092 Pgr progesterone receptor gene MP:0003572 abnormal uterus development IAGP N RGD:5509061 20141003 MGI PMID:24485460 11092 Pgr progesterone receptor gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20141003 MGI PMID:24474556 11092 Pgr progesterone receptor gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:11518735 11092 Pgr progesterone receptor gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:12438645 11092 Pgr progesterone receptor gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:10976068 11092 Pgr progesterone receptor gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:17045797 11092 Pgr progesterone receptor gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:23079602 11092 Pgr progesterone receptor gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:7557380 11092 Pgr progesterone receptor gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20190215 MGI PMID:27018534 11092 Pgr progesterone receptor gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20190321 MGI PMID:30626716 11092 Pgr progesterone receptor gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220120 MGI PMID:31875883 11092 Pgr progesterone receptor gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220203 MGI PMID:20484741 11092 Pgr progesterone receptor gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220303 MGI PMID:22233806 11092 Pgr progesterone receptor gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220512 MGI PMID:27783953 11092 Pgr progesterone receptor gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220602 MGI PMID:33590845 11092 Pgr progesterone receptor gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220915 MGI PMID:30213224 11092 Pgr progesterone receptor gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20230302 MGI PMID:35194044 11092 Pgr progesterone receptor gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20220922 MGI PMID:35654036 11092 Pgr progesterone receptor gene MP:0003967 abnormal follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10433223 11092 Pgr progesterone receptor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20230302 MGI PMID:35194044 11092 Pgr progesterone receptor gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:10976068 11092 Pgr progesterone receptor gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20220602 MGI PMID:33590845 11092 Pgr progesterone receptor gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:18276762 11092 Pgr progesterone receptor gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20170622 MGI PMID:25043182 11092 Pgr progesterone receptor gene MP:0004514 dystocia IAGP N RGD:5509061 20211209 MGI PMID:30954472 11092 Pgr progesterone receptor gene MP:0004514 dystocia IAGP N RGD:5509061 20220519 MGI PMID:35349646 11092 Pgr progesterone receptor gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18632614 11092 Pgr progesterone receptor gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19439667 11092 Pgr progesterone receptor gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20418913 11092 Pgr progesterone receptor gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20160728 MGI PMID:25377472 11092 Pgr progesterone receptor gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:11518735 11092 Pgr progesterone receptor gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:20418913 11092 Pgr progesterone receptor gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:21209023 11092 Pgr progesterone receptor gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20180315 MGI PMID:28005395 11092 Pgr progesterone receptor gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20190215 MGI PMID:27018534 11092 Pgr progesterone receptor gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20190321 MGI PMID:30626716 11092 Pgr progesterone receptor gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20211209 MGI PMID:30954472 11092 Pgr progesterone receptor gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20220512 MGI PMID:27783953 11092 Pgr progesterone receptor gene MP:0004902 abnormal uterus size IAGP N RGD:5509061 20141003 MGI PMID:21209023 11092 Pgr progesterone receptor gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:19439667 11092 Pgr progesterone receptor gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:20418913 11092 Pgr progesterone receptor gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20150709 MGI PMID:23820898 11092 Pgr progesterone receptor gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20160728 MGI PMID:25377472 11092 Pgr progesterone receptor gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:21209023 11092 Pgr progesterone receptor gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20160728 MGI PMID:25377472 11092 Pgr progesterone receptor gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:18632614 11092 Pgr progesterone receptor gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20150709 MGI PMID:23820898 11092 Pgr progesterone receptor gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:18276762 11092 Pgr progesterone receptor gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20230302 MGI PMID:35194044 11092 Pgr progesterone receptor gene MP:0005124 increased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:12897242 11092 Pgr progesterone receptor gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20180315 MGI PMID:28005395 11092 Pgr progesterone receptor gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12438645 11092 Pgr progesterone receptor gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:18276762 11092 Pgr progesterone receptor gene MP:0005489 vascular smooth muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11518735 11092 Pgr progesterone receptor gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12438645 11092 Pgr progesterone receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12438645 11092 Pgr progesterone receptor gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:18276762 11092 Pgr progesterone receptor gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:12897242 11092 Pgr progesterone receptor gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24474556 11092 Pgr progesterone receptor gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20150709 MGI PMID:23820898 11092 Pgr progesterone receptor gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20150709 MGI PMID:23820898 11092 Pgr progesterone receptor gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18276762 11092 Pgr progesterone receptor gene MP:0008870 increased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:7557380 11092 Pgr progesterone receptor gene MP:0008876 decreased uterine NK cell number IAGP N RGD:5509061 20180315 MGI PMID:28005395 11092 Pgr progesterone receptor gene MP:0008876 decreased uterine NK cell number IAGP N RGD:5509061 20211209 MGI PMID:30954472 11092 Pgr progesterone receptor gene MP:0008876 decreased uterine NK cell number IAGP N RGD:5509061 20230302 MGI PMID:35194044 11092 Pgr progesterone receptor gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20230302 MGI PMID:35194044 11092 Pgr progesterone receptor gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20180315 MGI PMID:28005395 11092 Pgr progesterone receptor gene MP:0009080 uterus inflammation IAGP N RGD:5509061 20141003 MGI PMID:7557380 11092 Pgr progesterone receptor gene MP:0009080 uterus inflammation IAGP N RGD:5509061 20190215 MGI PMID:27018534 11092 Pgr progesterone receptor gene MP:0009082 uterus cyst IAGP N RGD:5509061 20180315 MGI PMID:28005395 11092 Pgr progesterone receptor gene MP:0009082 uterus cyst IAGP N RGD:5509061 20190215 MGI PMID:27018534 11092 Pgr progesterone receptor gene MP:0009088 thin uterine horn IAGP N RGD:5509061 20141003 MGI PMID:21209023 11092 Pgr progesterone receptor gene MP:0009091 endometrium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21209023 11092 Pgr progesterone receptor gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18632614 11092 Pgr progesterone receptor gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19439667 11092 Pgr progesterone receptor gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20418913 11092 Pgr progesterone receptor gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:24474556 11092 Pgr progesterone receptor gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20150709 MGI PMID:23820898 11092 Pgr progesterone receptor gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20160728 MGI PMID:25377472 11092 Pgr progesterone receptor gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20211209 MGI PMID:30954472 11092 Pgr progesterone receptor gene MP:0009094 abnormal endometrial gland morphology IAGP N RGD:5509061 20180315 MGI PMID:28005395 11092 Pgr progesterone receptor gene MP:0009094 abnormal endometrial gland morphology IAGP N RGD:5509061 20190215 MGI PMID:27018534 11092 Pgr progesterone receptor gene MP:0009094 abnormal endometrial gland morphology IAGP N RGD:5509061 20211209 MGI PMID:30954472 11092 Pgr progesterone receptor gene MP:0009094 abnormal endometrial gland morphology IAGP N RGD:5509061 20220602 MGI PMID:33590845 11092 Pgr progesterone receptor gene MP:0009096 decreased endometrial gland number IAGP N RGD:5509061 20220203 MGI PMID:20484741 11092 Pgr progesterone receptor gene MP:0009097 absent endometrial glands IAGP N RGD:5509061 20141003 MGI PMID:21508348 11092 Pgr progesterone receptor gene MP:0009209 abnormal internal female genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:24474556 11092 Pgr progesterone receptor gene MP:0009251 enlarged endometrial glands IAGP N RGD:5509061 20141003 MGI PMID:7557380 11092 Pgr progesterone receptor gene MP:0009251 enlarged endometrial glands IAGP N RGD:5509061 20180315 MGI PMID:28005395 11092 Pgr progesterone receptor gene MP:0009251 enlarged endometrial glands IAGP N RGD:5509061 20190215 MGI PMID:27018534 11092 Pgr progesterone receptor gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:18276762 11092 Pgr progesterone receptor gene MP:0009352 impaired spacing of implantation sites IAGP N RGD:5509061 20170622 MGI PMID:25043182 11092 Pgr progesterone receptor gene MP:0009353 twin decidual capsule IAGP N RGD:5509061 20170622 MGI PMID:25043182 11092 Pgr progesterone receptor gene MP:0009360 endometrium inflammation IAGP N RGD:5509061 20220602 MGI PMID:33590845 11092 Pgr progesterone receptor gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:21862609 11092 Pgr progesterone receptor gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12897242 11092 Pgr progesterone receptor gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14667968 11092 Pgr progesterone receptor gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12897242 11092 Pgr progesterone receptor gene MP:0009649 delayed embryo implantation IAGP N RGD:5509061 20220602 MGI PMID:33590845 11092 Pgr progesterone receptor gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20220602 MGI PMID:33590845 11092 Pgr progesterone receptor gene MP:0009662 abnormal uterine receptivity IAGP N RGD:5509061 20141003 MGI PMID:23079602 11092 Pgr progesterone receptor gene MP:0009662 abnormal uterine receptivity IAGP N RGD:5509061 20190321 MGI PMID:30626716 11092 Pgr progesterone receptor gene MP:0009662 abnormal uterine receptivity IAGP N RGD:5509061 20220303 MGI PMID:22233806 11092 Pgr progesterone receptor gene MP:0009663 abnormal uterine-embryonic axis IAGP N RGD:5509061 20170622 MGI PMID:25043182 11092 Pgr progesterone receptor gene MP:0009663 abnormal uterine-embryonic axis IAGP N RGD:5509061 20220602 MGI PMID:33590845 11092 Pgr progesterone receptor gene MP:0009664 abnormal luminal closure IAGP N RGD:5509061 20141003 MGI PMID:23079602 11092 Pgr progesterone receptor gene MP:0009664 abnormal luminal closure IAGP N RGD:5509061 20220602 MGI PMID:33590845 11092 Pgr progesterone receptor gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20170622 MGI PMID:25043182 11092 Pgr progesterone receptor gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20190321 MGI PMID:30626716 11092 Pgr progesterone receptor gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20220303 MGI PMID:22233806 11092 Pgr progesterone receptor gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20220602 MGI PMID:33590845 11092 Pgr progesterone receptor gene MP:0009667 abnormal embryo invasion IAGP N RGD:5509061 20220203 MGI PMID:20484741 11092 Pgr progesterone receptor gene MP:0009669 abnormal postimplantation uterine environment IAGP N RGD:5509061 20141003 MGI PMID:21508348 11092 Pgr progesterone receptor gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20141003 MGI PMID:20029965 11092 Pgr progesterone receptor gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20141003 MGI PMID:20962251 11092 Pgr progesterone receptor gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20141003 MGI PMID:24485460 11092 Pgr progesterone receptor gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20160728 MGI PMID:20418913 11092 Pgr progesterone receptor gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20160728 MGI PMID:25377472 11092 Pgr progesterone receptor gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20190321 MGI PMID:30626716 11092 Pgr progesterone receptor gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20220203 MGI PMID:20484741 11092 Pgr progesterone receptor gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20220512 MGI PMID:27783953 11092 Pgr progesterone receptor gene MP:0010039 abnormal trophoblast giant cell proliferation IAGP N RGD:5509061 20170622 MGI PMID:25043182 11092 Pgr progesterone receptor gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12897242 11092 Pgr progesterone receptor gene MP:0010287 increased reproductive system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24474556 11092 Pgr progesterone receptor gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20170622 MGI PMID:25043182 11092 Pgr progesterone receptor gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20150611 MGI PMID:12438645 11092 Pgr progesterone receptor gene MP:0011873 enlarged uterine horn IAGP N RGD:5509061 20190215 MGI PMID:27018534 11092 Pgr progesterone receptor gene MP:0011873 enlarged uterine horn IAGP N RGD:5509061 20211209 MGI PMID:30954472 11092 Pgr progesterone receptor gene MP:0012008 delayed parturition IAGP N RGD:5509061 20220519 MGI PMID:35349646 11092 Pgr progesterone receptor gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24474556 11092 Pgr progesterone receptor gene MP:0013399 endometrium fibrosis IAGP N RGD:5509061 20190321 MGI PMID:30626716 11092 Pgr progesterone receptor gene MP:0013400 abnormal endometrial gland development IAGP N RGD:5509061 20190215 MGI PMID:27018534 11092 Pgr progesterone receptor gene MP:0013400 abnormal endometrial gland development IAGP N RGD:5509061 20220203 MGI PMID:20484741 11092 Pgr progesterone receptor gene MP:0013401 increased endometrial gland number IAGP N RGD:5509061 20141218 MGI PMID:19439667 11092 Pgr progesterone receptor gene MP:0013401 increased endometrial gland number IAGP N RGD:5509061 20141218 MGI PMID:20962251 11092 Pgr progesterone receptor gene MP:0013401 increased endometrial gland number IAGP N RGD:5509061 20150709 MGI PMID:23820898 11092 Pgr progesterone receptor gene MP:0013401 increased endometrial gland number IAGP N RGD:5509061 20180315 MGI PMID:28005395 11092 Pgr progesterone receptor gene MP:0013401 increased endometrial gland number IAGP N RGD:5509061 20211209 MGI PMID:30954472 11092 Pgr progesterone receptor gene MP:0013401 increased endometrial gland number IAGP N RGD:5509061 20230302 MGI PMID:35194044 11092 Pgr progesterone receptor gene MP:0020253 increased collagen level IAGP N RGD:5509061 20190321 MGI PMID:30626716 11092 Pgr progesterone receptor gene MP:0031336 abnormal uterine epithelium development IAGP N RGD:5509061 20220120 MGI PMID:30954472 11092 Pgr progesterone receptor gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:10976068 11092 Pgr progesterone receptor gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220804 MGI PMID:16868919 11092 Pgr progesterone receptor gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220804 MGI PMID:20029965 11092 Pgr progesterone receptor gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220804 MGI PMID:7557380 11092 Pgr progesterone receptor gene MP:0031434 increased miscarriage rate IAGP N RGD:5509061 20230302 MGI PMID:35194044 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210826 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000202 abnormal circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:8106172 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000203 abnormal circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:8106172 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20150326 MGI PMID:14752830 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:7977654 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20150326 MGI PMID:14752830 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8106172 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20150326 MGI PMID:21292027 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000610 cholestasis IAGP N RGD:5509061 20141003 MGI PMID:7977654 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000610 cholestasis IAGP N RGD:5509061 20150326 MGI PMID:25068656 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20150903 MGI PMID:25478810 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0001263 weight loss IAGP N RGD:5509061 20150903 MGI PMID:25478810 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0001569 abnormal circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:8106172 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:11368757 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20150326 MGI PMID:14752830 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0001573 abnormal circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:8106172 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:7977654 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20150326 MGI PMID:21292027 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:8106172 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20150326 MGI PMID:21292027 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:7977654 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11368757 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002138 abnormal hepatobiliary system morphology IAGP N RGD:5509061 20141003 MGI PMID:7977654 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002139 abnormal hepatobiliary system physiology IAGP N RGD:5509061 20141003 MGI PMID:7977654 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:11368757 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:15930516 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002830 gallstones IAGP N RGD:5509061 20150326 MGI PMID:14752830 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:8106172 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20150326 MGI PMID:14752830 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:11368757 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:15930516 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20150326 MGI PMID:21292027 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20150326 MGI PMID:25068656 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20150903 MGI PMID:25478810 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20150326 MGI PMID:21292027 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20150326 MGI PMID:14752830 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20150326 MGI PMID:25068656 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20150903 MGI PMID:25478810 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20150326 MGI PMID:25068656 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003046 liver cirrhosis IAGP N RGD:5509061 20150903 MGI PMID:25478810 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20141003 MGI PMID:8106172 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20150326 MGI PMID:14752830 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003254 bile duct inflammation IAGP N RGD:5509061 20141003 MGI PMID:7977654 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003254 bile duct inflammation IAGP N RGD:5509061 20141003 MGI PMID:8106172 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003254 bile duct inflammation IAGP N RGD:5509061 20150326 MGI PMID:14752830 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003254 bile duct inflammation IAGP N RGD:5509061 20150326 MGI PMID:20921947 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003254 bile duct inflammation IAGP N RGD:5509061 20150326 MGI PMID:21292027 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20141003 MGI PMID:7977654 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20150326 MGI PMID:25068656 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003256 biliary cirrhosis IAGP N RGD:5509061 20141003 MGI PMID:7977654 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003328 portal hypertension IAGP N RGD:5509061 20150903 MGI PMID:25478810 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7977654 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20150903 MGI PMID:25478810 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20150326 MGI PMID:20921947 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20150326 MGI PMID:25068656 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20150903 MGI PMID:25478810 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:15930516 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7977654 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20150326 MGI PMID:25068656 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20141003 MGI PMID:8106172 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:15930516 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:8106172 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20150326 MGI PMID:14752830 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20150326 MGI PMID:21292027 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20150326 MGI PMID:25068656 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210128 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11368757 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:11368757 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:15930516 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20150903 MGI PMID:25478810 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:11368757 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20150326 MGI PMID:14752830 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20150326 MGI PMID:25068656 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20150903 MGI PMID:25478810 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20150326 MGI PMID:25068656 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20141003 MGI PMID:8106172 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20150326 MGI PMID:14752830 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20150326 MGI PMID:21292027 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20210128 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210826 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210826 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20150326 MGI PMID:20921947 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20230601 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0008837 increased transforming growth factor beta level IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0008991 abnormal bile canaliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:7977654 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0008991 abnormal bile canaliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:8106172 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0008993 abnormal portal triad morphology IAGP N RGD:5509061 20141003 MGI PMID:7977654 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8106172 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20150326 MGI PMID:21292027 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0010877 abnormal trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0011977 abnormal sodium ion homeostasis IAGP N RGD:5509061 20150326 MGI PMID:21292027 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0012336 decreased vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0012338 decreased bile salt level IAGP N RGD:5509061 20150326 MGI PMID:21292027 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0014476 abnormal feces lipid level IAGP N RGD:5509061 20240704 MGI PMID:15930516 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0014478 increased feces bile salt level IAGP N RGD:5509061 20240704 MGI PMID:21292027 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0014479 decreased feces bile salt level IAGP N RGD:5509061 20240704 MGI PMID:21292027 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:23545228 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0020134 abnormal gallbladder size IAGP N RGD:5509061 20150326 MGI PMID:14752830 11094 Abcb4 ATP-binding cassette, sub-family B member 4 gene MP:0021029 increased tumor necrosis factor (ligand) superfamily member 11 level IAGP N RGD:5509061 20220106 MGI PMID:23545228 11096 Phb1 prohibitin 1 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:17932104 11096 Phb1 prohibitin 1 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:21209023 11096 Phb1 prohibitin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21209023 11096 Phb1 prohibitin 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:21209023 11096 Phb1 prohibitin 1 gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:21209023 11096 Phb1 prohibitin 1 gene MP:0004902 abnormal uterus size IAGP N RGD:5509061 20141003 MGI PMID:21209023 11096 Phb1 prohibitin 1 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:21209023 11096 Phb1 prohibitin 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 11096 Phb1 prohibitin 1 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20231207 MGI 11096 Phb1 prohibitin 1 gene MP:0009088 thin uterine horn IAGP N RGD:5509061 20141003 MGI PMID:21209023 11096 Phb1 prohibitin 1 gene MP:0009091 endometrium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21209023 11096 Phb1 prohibitin 1 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 11096 Phb1 prohibitin 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21209023 11096 Phb1 prohibitin 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17932104 11096 Phb1 prohibitin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 11096 Phb1 prohibitin 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21209023 11096 Phb1 prohibitin 1 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20231207 MGI 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:18289812 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17710565 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22161748 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20181004 MGI PMID:29735309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:1962291 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000091 short premaxilla IAGP N RGD:5509061 20141003 MGI PMID:1962291 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:15579309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:22161748 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20220915 MGI PMID:17710565 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:11713245 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:14751570 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:15976027 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:17710565 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:18172553 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:22161748 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:22527485 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:3460077 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:8266820 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20181004 MGI PMID:29735309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:18289812 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:1962291 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:1962291 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:15579309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:17710565 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17710565 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8266820 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17710565 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18289812 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22527485 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:22527485 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18289812 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:18289812 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001562 abnormal circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001565 abnormal circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:15579309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:3145795 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:8266820 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001849 ear inflammation IAGP N RGD:5509061 20141003 MGI PMID:18289812 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:18289812 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:17710565 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:14751570 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:1962291 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:18289812 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:11713245 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:15579309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:17710565 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:3460077 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20181004 MGI PMID:29735309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20181004 MGI PMID:29735309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:22527485 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:22161748 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:22527485 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:3460077 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20181004 MGI PMID:29735309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:15579309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:18172553 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:22161748 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:11713245 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:15976027 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003167 abnormal scala tympani morphology IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15976027 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003432 increased activity of parathyroid IAGP N RGD:5509061 20181004 MGI PMID:29735309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003620 oliguria IAGP N RGD:5509061 20181004 MGI PMID:29735309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:14751570 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22161748 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22161748 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20181004 MGI PMID:29735309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:11713245 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004338 small clavicle IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004348 long femur IAGP N RGD:5509061 20141003 MGI PMID:15579309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004348 long femur IAGP N RGD:5509061 20181011 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004380 short frontal bone IAGP N RGD:5509061 20141003 MGI PMID:1962291 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:1962291 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004652 small caudal vertebrae IAGP N RGD:5509061 20141003 MGI PMID:14751570 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:18172553 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:22161748 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004699 unilateral deafness IAGP N RGD:5509061 20141003 MGI PMID:18289812 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0005353 abnormal patella morphology IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17710565 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0005628 decreased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0006025 distended Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:18289812 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:18289812 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20181004 MGI PMID:29735309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20231130 MGI PMID:17710565 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:18289812 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:17710565 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0006431 abnormal fibrocartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:23038738 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:15579309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:15579309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:22161748 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:1962291 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0009445 osteomalacia IAGP N RGD:5509061 20141003 MGI PMID:11713245 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0009445 osteomalacia IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0009445 osteomalacia IAGP N RGD:5509061 20141003 MGI PMID:14751570 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0009445 osteomalacia IAGP N RGD:5509061 20141003 MGI PMID:18172553 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0009445 osteomalacia IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20181004 MGI PMID:29735309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20160310 MGI PMID:15976027 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0009877 exostosis IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0010110 abnormal renal phosphate reabsorption IAGP N RGD:5509061 20141003 MGI PMID:18172553 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20220915 MGI PMID:17710565 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0010924 abnormal osteoid morphology IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0011221 decreased intestinal calcium absorption IAGP N RGD:5509061 20141003 MGI PMID:8266820 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:16449303 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0011447 abnormal renal glucose reabsorption IAGP N RGD:5509061 20141003 MGI PMID:3460077 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0011470 increased urine creatinine level IAGP N RGD:5509061 20181004 MGI PMID:29735309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0011476 abnormal urine nucleotide level IAGP N RGD:5509061 20141003 MGI PMID:3460077 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0011504 abnormal limb long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0011505 camptomelia IAGP N RGD:5509061 20141003 MGI PMID:22573557 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18289812 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0012336 decreased vitamin D level IAGP N RGD:5509061 20181004 MGI PMID:29735309 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0013942 enthesitis IAGP N RGD:5509061 20160310 MGI PMID:23038738 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0014104 decreased chondrocyte apoptosis IAGP N RGD:5509061 20171221 MGI PMID:17710565 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:15029877 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:17710565 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:22527485 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:11159866 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0021186 decreased bone mineral density of vertebrae IAGP N RGD:5509061 20220915 MGI PMID:17710565 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0030484 abnormal osteocyte lacuna morphology IAGP N RGD:5509061 20171221 MGI PMID:18172553 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0030485 abnormal osteocyte lacunocanalicular system morphology IAGP N RGD:5509061 20171221 MGI PMID:18172553 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0030828 abnormal obturator foramen morphology IAGP N RGD:5509061 20181018 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0030830 abnormal acetabulum morphology IAGP N RGD:5509061 20181018 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0030876 abnormal costochondral joint morphology IAGP N RGD:5509061 20181101 MGI PMID:12414538 11097 Phex phosphate regulating endopeptidase homolog, X-linked gene MP:0031060 decreased circulating C-reactive protein level IAGP N RGD:5509061 20200618 MGI PMID:29735309 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10377440 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0000111 cleft palate IAGP N RGD:5509061 20190822 MGI PMID:31232685 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:10092065 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:12692150 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:11535627 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:10092065 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10092065 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001124 abnormal gametes IAGP N RGD:5509061 20141003 MGI PMID:12692150 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:9207103 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:9207103 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:9207103 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20190530 MGI PMID:15304084 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:9207103 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11535627 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11535627 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11535627 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001429 dehydration IAGP N RGD:5509061 20190530 MGI PMID:15304084 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:10377440 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10092065 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:10092065 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20190530 MGI PMID:19679885 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:9207103 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12692150 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11535627 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10092065 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20190822 MGI PMID:31232685 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10556176 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20190530 MGI PMID:19679885 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10556176 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:10556176 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20190530 MGI PMID:15304084 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:11535627 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10556176 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:10377440 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0003950 abnormal plasma membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:8611683 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20190822 MGI PMID:31232685 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20190530 MGI PMID:15304084 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20190530 MGI PMID:19679885 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20190530 MGI PMID:15304084 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20190530 MGI PMID:19679885 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9207103 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10556176 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10092065 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8611683 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0031010 failure of sperm-egg fusion IAGP N RGD:5509061 20200130 MGI PMID:12692150 11100 Piga phosphatidylinositol glycan anchor biosynthesis, class A gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:10556176 11102 Pigr polymeric immunoglobulin receptor gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:12594279 11102 Pigr polymeric immunoglobulin receptor gene MP:0000501 abnormal digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:17056558 11102 Pigr polymeric immunoglobulin receptor gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12594279 11102 Pigr polymeric immunoglobulin receptor gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10510081 11102 Pigr polymeric immunoglobulin receptor gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:10510081 11102 Pigr polymeric immunoglobulin receptor gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:10553061 11102 Pigr polymeric immunoglobulin receptor gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12594279 11102 Pigr polymeric immunoglobulin receptor gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:16569672 11102 Pigr polymeric immunoglobulin receptor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16569672 11102 Pigr polymeric immunoglobulin receptor gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:10510081 11102 Pigr polymeric immunoglobulin receptor gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12594279 11102 Pigr polymeric immunoglobulin receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:10510081 11102 Pigr polymeric immunoglobulin receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:10553061 11102 Pigr polymeric immunoglobulin receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12594279 11102 Pigr polymeric immunoglobulin receptor gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:10510081 11102 Pigr polymeric immunoglobulin receptor gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:10553061 11102 Pigr polymeric immunoglobulin receptor gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12594279 11102 Pigr polymeric immunoglobulin receptor gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15770700 11102 Pigr polymeric immunoglobulin receptor gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:16569672 11102 Pigr polymeric immunoglobulin receptor gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:17056558 11102 Pigr polymeric immunoglobulin receptor gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:10553061 11102 Pigr polymeric immunoglobulin receptor gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15770700 11102 Pigr polymeric immunoglobulin receptor gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15770700 11102 Pigr polymeric immunoglobulin receptor gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17056558 11102 Pigr polymeric immunoglobulin receptor gene MP:0008401 abnormal CD8 positive, alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15770700 11102 Pigr polymeric immunoglobulin receptor gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16569672 11102 Pigr polymeric immunoglobulin receptor gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16569672 11102 Pigr polymeric immunoglobulin receptor gene MP:0008895 abnormal intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:15770700 11102 Pigr polymeric immunoglobulin receptor gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:10510081 11102 Pigr polymeric immunoglobulin receptor gene MP:0010223 abnormal immunoglobulin transcytosis IAGP N RGD:5509061 20141003 MGI PMID:10510081 11102 Pigr polymeric immunoglobulin receptor gene MP:0010223 abnormal immunoglobulin transcytosis IAGP N RGD:5509061 20141003 MGI PMID:12594279 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11062485 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:9988280 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0000245 abnormal erythropoiesis IEA N RGD:5509061 20111116 MGI 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20200109 MGI PMID:21398281 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20161124 MGI PMID:27708159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16354682 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:11062485 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:9888854 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16354682 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9888855 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11062485 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14673165 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9888854 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14673165 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16354682 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16227599 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9888854 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16114097 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11062485 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14673165 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9988280 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20161124 MGI PMID:27708159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:16227599 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:11062485 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:14673165 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:9988280 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20161124 MGI PMID:27708159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11062485 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:16227599 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0004978 decreased B-1 B cell number IEA N RGD:5509061 20180215 MGI 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9888854 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16114097 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9888854 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9888855 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11062485 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14673165 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:14673165 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:9988280 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20161124 MGI PMID:27708159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19029981 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20180215 MGI 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008168 decreased B-1a cell number IEA N RGD:5509061 20180215 MGI 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20180215 MGI 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008170 decreased B-1b cell number IEA N RGD:5509061 20180215 MGI 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16354682 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20180215 MGI 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:9888854 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16354682 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:9888854 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16354682 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9888854 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9888855 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16354682 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20200109 MGI PMID:21398281 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16354682 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14673165 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:11062485 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20200109 MGI PMID:21398281 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20180215 MGI 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19029981 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20180215 MGI 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9888855 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0011089 perinatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16354682 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0012080 chylous ascites IAGP N RGD:5509061 20141003 MGI PMID:11062485 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200109 MGI PMID:21398281 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20161124 MGI PMID:27708159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0020359 abnormal ribbon synapse morphology IAGP N RGD:5509061 20200109 MGI PMID:21398281 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:9988280 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20190215 MGI PMID:26974159 11103 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1 gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:9988280 11104 Pim1 proviral integration site 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:8233823 11104 Pim1 proviral integration site 1 gene MP:0001588 abnormal hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:8233823 11104 Pim1 proviral integration site 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15199164 11104 Pim1 proviral integration site 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23509290 11104 Pim1 proviral integration site 1 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:15199164 11104 Pim1 proviral integration site 1 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7689870 11104 Pim1 proviral integration site 1 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8361211 11104 Pim1 proviral integration site 1 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:15199164 11104 Pim1 proviral integration site 1 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:8233823 11104 Pim1 proviral integration site 1 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 11104 Pim1 proviral integration site 1 gene MP:0003133 increased early pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 11104 Pim1 proviral integration site 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 11104 Pim1 proviral integration site 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15199164 11104 Pim1 proviral integration site 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15199164 11104 Pim1 proviral integration site 1 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 11104 Pim1 proviral integration site 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 11104 Pim1 proviral integration site 1 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 11104 Pim1 proviral integration site 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15199164 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000088 short mandible IAGP N RGD:5509061 20180111 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000091 short premaxilla IAGP N RGD:5509061 20180111 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000097 short maxilla IAGP N RGD:5509061 20180111 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000276 heart right ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:12095915 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000299 failure of atrioventricular cushion closure IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:9326937 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17575307 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000608 dissociated hepatocytes IAGP N RGD:5509061 20141003 MGI PMID:9988265 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19774080 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:19774080 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:19774080 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9326937 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15496422 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16400024 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18003909 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16400024 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:15496422 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:16400024 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:18003909 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:9326937 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:18263604 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10677526 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12140187 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:20862291 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:20862291 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15496422 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16400024 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17575307 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:15579506 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:11818962 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:12140187 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15579506 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:18385665 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19774080 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20862291 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:10677526 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:12095915 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:17928412 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:15496422 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:9988265 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:19774080 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10677526 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12140187 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15579506 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19774080 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20862291 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:16400024 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:20862291 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9326937 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18003909 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15496422 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16400024 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17575307 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18003909 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18385665 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002083 premature death IAGP N RGD:5509061 20151203 MGI PMID:25574838 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002083 premature death IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:16400024 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16400024 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:18263604 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:20075061 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:20562878 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:23236168 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15496422 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19255143 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19774080 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:10677526 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:9326937 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002639 micrognathia IEA N RGD:5509061 20141003 MGI 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:17928412 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:17932118 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18003909 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:23439951 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:9988265 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20200310 MGI PMID:30799240 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:9988265 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:11818962 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:16400024 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:17575307 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:18003909 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:20075061 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:23236168 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:9326937 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15496422 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16400024 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9988265 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:20862291 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20141003 MGI PMID:15496422 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003254 bile duct inflammation IAGP N RGD:5509061 20141003 MGI PMID:9988265 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003266 biliary cyst IAGP N RGD:5509061 20141003 MGI PMID:15496422 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003325 decreased liver function IAGP N RGD:5509061 20141003 MGI PMID:9988265 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:12140187 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:15579506 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:17575307 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:17928412 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:17932118 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:9988265 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003334 pancreas fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:10677526 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:12007403 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:12140187 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:15496422 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:15579506 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:16400024 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:17575307 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:17928412 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:9326937 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003338 pancreas lipomatosis IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18579360 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003432 increased activity of parathyroid IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20141003 MGI PMID:11818962 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003602 increased renal hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:18263604 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:19774080 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:9326937 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003674 oxidative stress IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:10677526 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:11818962 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12007403 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12095915 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12140187 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12514735 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:15496422 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:15579506 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:16400024 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17575307 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17928412 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17932118 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18263604 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:19774080 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:20075061 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:20862291 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:21685914 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:9326937 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:9988265 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141030 MGI PMID:24700869 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003675 kidney cyst IAGP N RGD:5509061 20240328 MGI PMID:37953472 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:12140187 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18579360 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:17932118 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:18263604 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:21685914 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141030 MGI PMID:24700869 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20151203 MGI PMID:25574838 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20200310 MGI PMID:30799240 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20075061 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004020 polyhydramnios IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004020 polyhydramnios IAGP N RGD:5509061 20141003 MGI PMID:15579506 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004020 polyhydramnios IAGP N RGD:5509061 20141003 MGI PMID:16301212 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004020 polyhydramnios IAGP N RGD:5509061 20141003 MGI PMID:18385665 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004020 polyhydramnios IAGP N RGD:5509061 20141003 MGI PMID:20862291 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004044 aortic dissection IAGP N RGD:5509061 20141003 MGI PMID:15496422 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18385665 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004380 short frontal bone IAGP N RGD:5509061 20180111 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004451 short presphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004471 short nasal bone IAGP N RGD:5509061 20180111 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:17575307 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:21685914 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19774080 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004967 abnormal kidney epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12514735 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:17932118 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18263604 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005328 abnormal circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:9988265 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:23236168 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18263604 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16400024 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18003909 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18263604 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:20075061 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:21685914 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23236168 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20151203 MGI PMID:25574838 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20180726 MGI PMID:21465620 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20200310 MGI PMID:30799240 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:18263604 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:15496422 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0006322 abnormal perichondrium morphology IAGP N RGD:5509061 20141003 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0006357 abnormal circulating mineral level IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:17932118 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:18003909 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:18263604 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:18385665 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:18579360 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:20562878 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:23236168 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:23439951 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20151203 MGI PMID:25574838 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20180726 MGI PMID:21465620 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20200310 MGI PMID:30799240 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:9326937 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:9326937 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0009164 exocrine pancreas atrophy IAGP N RGD:5509061 20150611 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:9326937 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0009495 abnormal common bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18003909 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0009644 uremia IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:19959710 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0010656 thick myocardium IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0010962 decreased compact bone mass IAGP N RGD:5509061 20141003 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18263604 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18579360 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19774080 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9326937 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12140187 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18385665 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20862291 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17575307 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20862291 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9326937 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15579506 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17932118 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18003909 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19255143 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10677526 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11593033 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12007403 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17928412 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19774080 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18385665 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12140187 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11689485 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12095915 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18385665 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20862291 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20141003 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20141003 MGI PMID:9326937 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011344 abnormal loop of Henle ascending limb thick segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21685914 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20075061 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20180222 MGI PMID:21685914 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20180726 MGI PMID:21465620 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20151203 MGI PMID:25574838 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17932118 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20075061 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20180222 MGI PMID:21685914 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20180726 MGI PMID:21465620 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20240328 MGI PMID:37953472 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0011744 abnormal kidney epithelial cell primary cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:12514735 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0012172 abnormal amniotic fluid composition IAGP N RGD:5509061 20141003 MGI PMID:16301212 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0014010 abnormal peroxisome morphology IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20190725 MGI PMID:28205547 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0020382 increased kidney epithelial cell primary cilium length IAGP N RGD:5509061 20161013 MGI PMID:23064367 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0030438 increased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:23029375 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0030444 premature cranial synchondrosis closure IAGP N RGD:5509061 20180111 MGI PMID:18579360 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0030445 abnormal sphenooccipital synchondrosis IAGP N RGD:5509061 20180111 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0030446 premature sphenooccipital synchondrosis closure IAGP N RGD:5509061 20180111 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0030447 abnormal presphenoid synchondrosis IAGP N RGD:5509061 20180111 MGI PMID:18652813 11105 Pkd1 polycystin 1, transient receptor potential channel interacting gene MP:0030448 premature presphenoid synchondrosis closure IAGP N RGD:5509061 20180111 MGI PMID:18652813 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:7492793 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:17466543 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:7492793 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:14595440 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23078545 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7492793 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17466543 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23078545 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:14595440 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:7492793 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:7579416 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10886019 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14595440 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23078545 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:7492793 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:14595440 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:17466543 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:23078545 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:7492793 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:17466543 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:7492793 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7492793 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:7579416 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23078545 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:14595440 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17466543 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20240125 MGI PMID:35988463 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0005286 decreased saturated fatty acids level IAGP N RGD:5509061 20240125 MGI PMID:35988463 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:7492793 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:7579416 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20141003 MGI PMID:7492793 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7492793 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7492793 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17998386 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20240125 MGI PMID:35988463 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0010035 increased erythrocyte clearance IAGP N RGD:5509061 20141003 MGI PMID:17466543 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0010751 decreased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17466543 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:7492793 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0020583 decreased ceramide level IAGP N RGD:5509061 20240125 MGI PMID:35988463 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:23078545 11113 Pklr pyruvate kinase liver and red blood cell gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240125 MGI PMID:35988463 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:12808451 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11249852 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18931664 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:18931664 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12808451 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:9832165 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9403693 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9403692 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9403693 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15996660 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:9403692 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12808451 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:12045263 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:11249852 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0003033 abnormal pulmonary vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:12045263 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:11249852 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:9403693 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:12808451 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12045263 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12808451 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:15996660 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:12808451 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15033900 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:12808451 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16172261 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:12045263 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15996660 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0005462 abnormal mast cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10220374 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:9403692 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:9403693 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:9403693 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:11274413 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16172261 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16172261 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:16172261 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:10220374 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9832165 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20191017 MGI PMID:24297180 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:11249852 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:12808451 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0010936 decreased airway resistance IAGP N RGD:5509061 20141003 MGI PMID:9403692 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:9832165 11116 Pla2g4a phospholipase A2, group IVA (cytosolic, calcium-dependent) gene MP:0012010 parturition failure IAGP N RGD:5509061 20141003 MGI PMID:9403692 11120 Plcb4 phospholipase C, beta 4 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9305844 11120 Plcb4 phospholipase C, beta 4 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:9305844 11120 Plcb4 phospholipase C, beta 4 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9305844 11120 Plcb4 phospholipase C, beta 4 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 11120 Plcb4 phospholipase C, beta 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9305844 11120 Plcb4 phospholipase C, beta 4 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 11120 Plcb4 phospholipase C, beta 4 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9305844 11120 Plcb4 phospholipase C, beta 4 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9861037 11120 Plcb4 phospholipase C, beta 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9305844 11120 Plcb4 phospholipase C, beta 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9861037 11120 Plcb4 phospholipase C, beta 4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9305844 11120 Plcb4 phospholipase C, beta 4 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:9861037 11120 Plcb4 phospholipase C, beta 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 11120 Plcb4 phospholipase C, beta 4 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:11551922 11120 Plcb4 phospholipase C, beta 4 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:8962098 11120 Plcb4 phospholipase C, beta 4 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230601 MGI 11120 Plcb4 phospholipase C, beta 4 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:9861037 11120 Plcb4 phospholipase C, beta 4 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:11551922 11120 Plcb4 phospholipase C, beta 4 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:9305844 11120 Plcb4 phospholipase C, beta 4 gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20141003 MGI PMID:9861037 11120 Plcb4 phospholipase C, beta 4 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 11120 Plcb4 phospholipase C, beta 4 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:8962098 11120 Plcb4 phospholipase C, beta 4 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 11120 Plcb4 phospholipase C, beta 4 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20181227 MGI 11120 Plcb4 phospholipase C, beta 4 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20181227 MGI 11120 Plcb4 phospholipase C, beta 4 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 11120 Plcb4 phospholipase C, beta 4 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 11120 Plcb4 phospholipase C, beta 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20181227 MGI 11120 Plcb4 phospholipase C, beta 4 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20181227 MGI 11120 Plcb4 phospholipase C, beta 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9305844 11120 Plcb4 phospholipase C, beta 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 11121 Plk1 polo like kinase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18794363 11121 Plk1 polo like kinase 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18794363 11121 Plk1 polo like kinase 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18794363 11121 Plk1 polo like kinase 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18794363 11121 Plk1 polo like kinase 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:18794363 11121 Plk1 polo like kinase 1 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18794363 11121 Plk1 polo like kinase 1 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18794363 11121 Plk1 polo like kinase 1 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:18794363 11121 Plk1 polo like kinase 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18794363 11121 Plk1 polo like kinase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 11121 Plk1 polo like kinase 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18794363 11121 Plk1 polo like kinase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 11121 Plk1 polo like kinase 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 11123 Plp2 proteolipid protein 2 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20161027 MGI PMID:26512060 11123 Plp2 proteolipid protein 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20161027 MGI PMID:26512060 11123 Plp2 proteolipid protein 2 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20161027 MGI PMID:26512060 11123 Plp2 proteolipid protein 2 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20161027 MGI PMID:26512060 11123 Plp2 proteolipid protein 2 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20161027 MGI PMID:26512060 11123 Plp2 proteolipid protein 2 gene MP:0030949 abnormal Golgi vesicle transport IAGP N RGD:5509061 20190725 MGI PMID:26512060 11125 Pmp22 peripheral myelin protein 22 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12359155 11125 Pmp22 peripheral myelin protein 22 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16436605 11125 Pmp22 peripheral myelin protein 22 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:22258617 11125 Pmp22 peripheral myelin protein 22 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:3388045 11125 Pmp22 peripheral myelin protein 22 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:6313869 11125 Pmp22 peripheral myelin protein 22 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:7581450 11125 Pmp22 peripheral myelin protein 22 gene MP:0000745 tremors IAGP N RGD:5509061 20180412 MGI PMID:22527485 11125 Pmp22 peripheral myelin protein 22 gene MP:0000745 tremors IAGP N RGD:5509061 20200123 MGI PMID:24539699 11125 Pmp22 peripheral myelin protein 22 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:16436605 11125 Pmp22 peripheral myelin protein 22 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:9147228 11125 Pmp22 peripheral myelin protein 22 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:16436605 11125 Pmp22 peripheral myelin protein 22 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:7581450 11125 Pmp22 peripheral myelin protein 22 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20200123 MGI PMID:24539699 11125 Pmp22 peripheral myelin protein 22 gene MP:0000756 forelimb paralysis IAGP N RGD:5509061 20200123 MGI PMID:24539699 11125 Pmp22 peripheral myelin protein 22 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15703401 11125 Pmp22 peripheral myelin protein 22 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15755691 11125 Pmp22 peripheral myelin protein 22 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:6313869 11125 Pmp22 peripheral myelin protein 22 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:7581450 11125 Pmp22 peripheral myelin protein 22 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:9147228 11125 Pmp22 peripheral myelin protein 22 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:9219937 11125 Pmp22 peripheral myelin protein 22 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:10932191 11125 Pmp22 peripheral myelin protein 22 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:12359155 11125 Pmp22 peripheral myelin protein 22 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:15363066 11125 Pmp22 peripheral myelin protein 22 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:16436605 11125 Pmp22 peripheral myelin protein 22 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:3388045 11125 Pmp22 peripheral myelin protein 22 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:9219937 11125 Pmp22 peripheral myelin protein 22 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:7581450 11125 Pmp22 peripheral myelin protein 22 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20200123 MGI PMID:24539699 11125 Pmp22 peripheral myelin protein 22 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9147228 11125 Pmp22 peripheral myelin protein 22 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12359155 11125 Pmp22 peripheral myelin protein 22 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15755691 11125 Pmp22 peripheral myelin protein 22 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16436605 11125 Pmp22 peripheral myelin protein 22 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17701891 11125 Pmp22 peripheral myelin protein 22 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:3388045 11125 Pmp22 peripheral myelin protein 22 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:6313869 11125 Pmp22 peripheral myelin protein 22 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9147228 11125 Pmp22 peripheral myelin protein 22 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9219937 11125 Pmp22 peripheral myelin protein 22 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200123 MGI PMID:24539699 11125 Pmp22 peripheral myelin protein 22 gene MP:0001393 ataxia IEA N RGD:5509061 20141003 MGI 11125 Pmp22 peripheral myelin protein 22 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12359155 11125 Pmp22 peripheral myelin protein 22 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12359155 11125 Pmp22 peripheral myelin protein 22 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17701891 11125 Pmp22 peripheral myelin protein 22 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12359155 11125 Pmp22 peripheral myelin protein 22 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16436605 11125 Pmp22 peripheral myelin protein 22 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:3388045 11125 Pmp22 peripheral myelin protein 22 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:6313869 11125 Pmp22 peripheral myelin protein 22 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9147228 11125 Pmp22 peripheral myelin protein 22 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9219937 11125 Pmp22 peripheral myelin protein 22 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200123 MGI PMID:24539699 11125 Pmp22 peripheral myelin protein 22 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16436605 11125 Pmp22 peripheral myelin protein 22 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:12359155 11125 Pmp22 peripheral myelin protein 22 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:6681440 11125 Pmp22 peripheral myelin protein 22 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:7581450 11125 Pmp22 peripheral myelin protein 22 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:12359155 11125 Pmp22 peripheral myelin protein 22 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16436605 11125 Pmp22 peripheral myelin protein 22 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200123 MGI PMID:24539699 11125 Pmp22 peripheral myelin protein 22 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200123 MGI PMID:24539699 11125 Pmp22 peripheral myelin protein 22 gene MP:0001967 deafness IEA N RGD:5509061 20141003 MGI 11125 Pmp22 peripheral myelin protein 22 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:6313869 11125 Pmp22 peripheral myelin protein 22 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:16436605 11125 Pmp22 peripheral myelin protein 22 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:6681440 11125 Pmp22 peripheral myelin protein 22 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:16436605 11125 Pmp22 peripheral myelin protein 22 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16436605 11125 Pmp22 peripheral myelin protein 22 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20180412 MGI PMID:22527485 11125 Pmp22 peripheral myelin protein 22 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:16436605 11125 Pmp22 peripheral myelin protein 22 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:7581450 11125 Pmp22 peripheral myelin protein 22 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:15363066 11125 Pmp22 peripheral myelin protein 22 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:7581450 11125 Pmp22 peripheral myelin protein 22 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:16436605 11125 Pmp22 peripheral myelin protein 22 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:17701891 11125 Pmp22 peripheral myelin protein 22 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:7581450 11125 Pmp22 peripheral myelin protein 22 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:12359155 11125 Pmp22 peripheral myelin protein 22 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20160714 MGI PMID:12090404 11125 Pmp22 peripheral myelin protein 22 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15748170 11125 Pmp22 peripheral myelin protein 22 gene MP:0006325 impaired hearing IEA N RGD:5509061 20141003 MGI 11125 Pmp22 peripheral myelin protein 22 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:17174099 11125 Pmp22 peripheral myelin protein 22 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:6681440 11125 Pmp22 peripheral myelin protein 22 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:7581450 11125 Pmp22 peripheral myelin protein 22 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:12359155 11125 Pmp22 peripheral myelin protein 22 gene MP:0010742 increased Schwann cell number IAGP N RGD:5509061 20160714 MGI PMID:12090404 11125 Pmp22 peripheral myelin protein 22 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20200123 MGI PMID:24539699 11125 Pmp22 peripheral myelin protein 22 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20160714 MGI PMID:12090404 11125 Pmp22 peripheral myelin protein 22 gene MP:0011904 abnormal Schwann cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15755691 11125 Pmp22 peripheral myelin protein 22 gene MP:0011906 increased Schwann cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15755691 11125 Pmp22 peripheral myelin protein 22 gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20141003 MGI 11125 Pmp22 peripheral myelin protein 22 gene MP:0012051 spasticity IEA N RGD:5509061 20141003 MGI 11125 Pmp22 peripheral myelin protein 22 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20160714 MGI PMID:12090404 11126 Pnmt phenylethanolamine-N-methyltransferase gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17698731 11126 Pnmt phenylethanolamine-N-methyltransferase gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:17698731 11126 Pnmt phenylethanolamine-N-methyltransferase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 11126 Pnmt phenylethanolamine-N-methyltransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22706789 11126 Pnmt phenylethanolamine-N-methyltransferase gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:17698731 11126 Pnmt phenylethanolamine-N-methyltransferase gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 11126 Pnmt phenylethanolamine-N-methyltransferase gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20141003 MGI PMID:17698731 11126 Pnmt phenylethanolamine-N-methyltransferase gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160421 MGI 11126 Pnmt phenylethanolamine-N-methyltransferase gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:15517585 11126 Pnmt phenylethanolamine-N-methyltransferase gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:17698731 11126 Pnmt phenylethanolamine-N-methyltransferase gene MP:0030762 decreased adrenaline level IAGP N RGD:5509061 20180927 MGI PMID:15517585 11127 Pole polymerase (DNA directed), epsilon gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19805137 11127 Pole polymerase (DNA directed), epsilon gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 11127 Pole polymerase (DNA directed), epsilon gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 11127 Pole polymerase (DNA directed), epsilon gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19805137 11127 Pole polymerase (DNA directed), epsilon gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 11127 Pole polymerase (DNA directed), epsilon gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 11127 Pole polymerase (DNA directed), epsilon gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 11127 Pole polymerase (DNA directed), epsilon gene MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 11127 Pole polymerase (DNA directed), epsilon gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 11127 Pole polymerase (DNA directed), epsilon gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 11127 Pole polymerase (DNA directed), epsilon gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 11127 Pole polymerase (DNA directed), epsilon gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 11127 Pole polymerase (DNA directed), epsilon gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19805137 11127 Pole polymerase (DNA directed), epsilon gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20111116 MGI 11127 Pole polymerase (DNA directed), epsilon gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19805137 11127 Pole polymerase (DNA directed), epsilon gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20151112 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:9779941 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:9779941 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:9779941 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9779941 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16556738 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:11718806 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:16577229 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0001967 deafness IAGP N RGD:5509061 20151112 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:9779941 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20151112 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20151112 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0003879 abnormal hair cell physiology IAGP N RGD:5509061 20151112 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:16556738 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0004367 abnormal strial intermediate cell morphology IAGP N RGD:5509061 20151112 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20151112 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20151112 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20151112 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0004413 absent cochlear microphonics IAGP N RGD:5509061 20151112 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0004466 short cochlear outer hair cells IAGP N RGD:5509061 20151112 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20151112 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20151112 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9300691 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:7075549 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:7285859 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0005138 decreased prolactin level IAGP N RGD:5509061 20141003 MGI PMID:7285859 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:9779941 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0008330 absent somatotrophs IAGP N RGD:5509061 20141003 MGI PMID:6194978 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0008333 absent lactotrophs IAGP N RGD:5509061 20141003 MGI PMID:6194978 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0008333 absent lactotrophs IAGP N RGD:5509061 20141003 MGI PMID:7075549 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0008338 decreased thyrotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:13819893 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0008365 adenohypophysis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16556738 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:16577229 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9779941 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:9779941 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220519 MGI 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0011968 decreased threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21840860 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0013344 increased pituitary gland apoptosis IAGP N RGD:5509061 20141211 MGI PMID:16556738 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0013808 abnormal tunnel of Corti morphology IAGP N RGD:5509061 20151112 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0013961 abnormal Hensen stripe morphology IAGP N RGD:5509061 20160310 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0014091 abnormal tectorial membrane striated-sheet matrix morphology IAGP N RGD:5509061 20160421 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20190704 MGI PMID:19176829 11129 Pou1f1 POU domain, class 1, transcription factor 1 gene MP:0030494 abnormal molar root morphology IAGP N RGD:5509061 20180125 MGI PMID:16577229 11131 Ppia peptidylprolyl isomerase A gene MP:0000495 abnormal colon morphology IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0001258 decreased body length IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0001297 microphthalmia IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0002731 megacolon IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0002834 decreased heart weight IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230119 MGI 11131 Ppia peptidylprolyl isomerase A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15308100 11131 Ppia peptidylprolyl isomerase A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15308100 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:16735444 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12773574 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16735444 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16735444 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9084440 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0002987 abnormal urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:16735444 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:16735444 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8627154 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16735444 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16735444 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16735444 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:8627154 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:8627154 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:8627154 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:12773574 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:12773574 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:12773574 11134 Ppp3ca protein phosphatase 3, catalytic subunit, alpha isoform gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16735444 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11904392 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12773574 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16648267 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12091710 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20240523 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12091710 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:11904392 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16648267 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0002619 abnormal lymphocyte morphology IEA N RGD:5509061 20190418 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0002833 increased heart weight IAGP N RGD:5509061 20170601 MGI PMID:27114035 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16648267 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20240523 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IEA N RGD:5509061 20161201 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:11904392 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:16648267 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:11904392 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16648267 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12091710 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12091710 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16648267 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170601 MGI PMID:27114035 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:16648267 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0005387 immune system phenotype IEA N RGD:5509061 20240523 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16648267 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0008037 abnormal T cell morphology IEA N RGD:5509061 20190418 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20240523 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12091710 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:12773574 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0009405 increased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:12773574 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:12773574 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20170601 MGI PMID:27114035 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20170601 MGI PMID:27114035 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0010766 abnormal NK cell physiology IEA N RGD:5509061 20161201 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0010839 decreased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20180215 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20240523 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0011822 increased CD8-positive, alpha-beta memory T cell proliferation IEA N RGD:5509061 20161201 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0013519 decreased CD4-positive NK T cell number IEA N RGD:5509061 20240523 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0013522 decreased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20240523 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0013764 decreased T-helper cell number IEA N RGD:5509061 20240523 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20240523 MGI 11135 Ppp3cb protein phosphatase 3, catalytic subunit, beta isoform gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20161201 MGI 11138 Ppy pancreatic polypeptide gene MP:0001488 increased startle reflex IEA N RGD:5509061 20181227 MGI 11138 Ppy pancreatic polypeptide gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 11138 Ppy pancreatic polypeptide gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210826 MGI 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0009568 abnormal red blood cell deformability IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0010035 increased erythrocyte clearance IAGP N RGD:5509061 20141003 MGI PMID:20881209 11139 Prkag1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:20881209 11140 Prkar1b protein kinase, cAMP dependent regulatory, type I beta gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:8548807 11140 Prkar1b protein kinase, cAMP dependent regulatory, type I beta gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:7568030 11140 Prkar1b protein kinase, cAMP dependent regulatory, type I beta gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9295392 11140 Prkar1b protein kinase, cAMP dependent regulatory, type I beta gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:9295392 11140 Prkar1b protein kinase, cAMP dependent regulatory, type I beta gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:9295392 11147 Prkcg protein kinase C, gamma gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20220224 MGI PMID:33478986 11147 Prkcg protein kinase C, gamma gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10979601 11147 Prkcg protein kinase C, gamma gene MP:0001393 ataxia IAGP N RGD:5509061 20220224 MGI PMID:33478986 11147 Prkcg protein kinase C, gamma gene MP:0001405 impaired coordination IAGP N RGD:5509061 20220224 MGI PMID:33478986 11147 Prkcg protein kinase C, gamma gene MP:0001406 abnormal gait IAGP N RGD:5509061 20220224 MGI PMID:33478986 11147 Prkcg protein kinase C, gamma gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:8269510 11147 Prkcg protein kinase C, gamma gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:8269510 11147 Prkcg protein kinase C, gamma gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:8269509 11147 Prkcg protein kinase C, gamma gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:7731960 11147 Prkcg protein kinase C, gamma gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:7731960 11147 Prkcg protein kinase C, gamma gene MP:0001987 alcohol preference IAGP N RGD:5509061 20141003 MGI PMID:11606660 11147 Prkcg protein kinase C, gamma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16106361 11147 Prkcg protein kinase C, gamma gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20220224 MGI PMID:33478986 11147 Prkcg protein kinase C, gamma gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:7731960 11147 Prkcg protein kinase C, gamma gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20392936 11147 Prkcg protein kinase C, gamma gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20220224 MGI PMID:33478986 11147 Prkcg protein kinase C, gamma gene MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:10195808 11147 Prkcg protein kinase C, gamma gene MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:10195808 11147 Prkcg protein kinase C, gamma gene MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:7731960 11147 Prkcg protein kinase C, gamma gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20141003 MGI PMID:11606660 11149 Prkg2 protein kinase, cGMP-dependent, type II gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:8953039 11149 Prkg2 protein kinase, cGMP-dependent, type II gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:8953039 11149 Prkg2 protein kinase, cGMP-dependent, type II gene MP:0000505 decreased digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:8953039 11149 Prkg2 protein kinase, cGMP-dependent, type II gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:8953039 11149 Prkg2 protein kinase, cGMP-dependent, type II gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:8953039 11149 Prkg2 protein kinase, cGMP-dependent, type II gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8953039 11149 Prkg2 protein kinase, cGMP-dependent, type II gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:8953039 11149 Prkg2 protein kinase, cGMP-dependent, type II gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:8953039 11149 Prkg2 protein kinase, cGMP-dependent, type II gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:8953039 11149 Prkg2 protein kinase, cGMP-dependent, type II gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:8953039 11149 Prkg2 protein kinase, cGMP-dependent, type II gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:8953039 11149 Prkg2 protein kinase, cGMP-dependent, type II gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:8953039 11149 Prkg2 protein kinase, cGMP-dependent, type II gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:8953039 11152 Prl prolactin gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9384572 11152 Prl prolactin gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:9384572 11152 Prl prolactin gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12399440 11152 Prl prolactin gene MP:0000635 pituitary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12399440 11152 Prl prolactin gene MP:0000636 enlarged pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:12399440 11152 Prl prolactin gene MP:0000636 enlarged pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:9724019 11152 Prl prolactin gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:9384572 11152 Prl prolactin gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:9384572 11152 Prl prolactin gene MP:0001746 abnormal pituitary secretion IAGP N RGD:5509061 20141003 MGI PMID:9724019 11152 Prl prolactin gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9384572 11152 Prl prolactin gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:9384572 11152 Prl prolactin gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12399440 11152 Prl prolactin gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:9724019 11152 Prl prolactin gene MP:0003371 decreased circulating estrogen level IAGP N RGD:5509061 20141003 MGI PMID:12399440 11152 Prl prolactin gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:9724019 11152 Prl prolactin gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:9724019 11152 Prl prolactin gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:9384572 11152 Prl prolactin gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:9724019 11152 Prl prolactin gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:9724019 11152 Prl prolactin gene MP:0005138 decreased prolactin level IAGP N RGD:5509061 20141003 MGI PMID:9384572 11152 Prl prolactin gene MP:0005138 decreased prolactin level IAGP N RGD:5509061 20141003 MGI PMID:9724019 11152 Prl prolactin gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:12399440 11152 Prl prolactin gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:9724019 11152 Prl prolactin gene MP:0008325 abnormal gonadotroph morphology IAGP N RGD:5509061 20141003 MGI PMID:12399440 11152 Prl prolactin gene MP:0008332 decreased lactotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9384572 11152 Prl prolactin gene MP:0008939 increased pituitary gland weight IAGP N RGD:5509061 20141003 MGI PMID:9724019 11152 Prl prolactin gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:9384572 11152 Prl prolactin gene MP:0009007 short estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:9384572 11152 Prl prolactin gene MP:0009014 prolonged proestrus IAGP N RGD:5509061 20141003 MGI PMID:9384572 11152 Prl prolactin gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20141003 MGI PMID:9384572 11152 Prl prolactin gene MP:0013336 pituitary gland hypertrophy IAGP N RGD:5509061 20141204 MGI PMID:12399440 11152 Prl prolactin gene MP:0031362 decreased prostate gland ventral lobe weight IAGP N RGD:5509061 20220303 MGI PMID:9724019 11153 Prl4a1 prolactin family 4, subfamily a, member 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15545614 11153 Prl4a1 prolactin family 4, subfamily a, member 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:15545614 11153 Prl4a1 prolactin family 4, subfamily a, member 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:15545614 11153 Prl4a1 prolactin family 4, subfamily a, member 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15545614 11153 Prl4a1 prolactin family 4, subfamily a, member 1 gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:15545614 11153 Prl4a1 prolactin family 4, subfamily a, member 1 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15545614 11157 Prlr prolactin receptor gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9886812 11157 Prlr prolactin receptor gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15388648 11157 Prlr prolactin receptor gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:11356702 11157 Prlr prolactin receptor gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:11356702 11157 Prlr prolactin receptor gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:11445538 11157 Prlr prolactin receptor gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:9009200 11157 Prlr prolactin receptor gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:16166330 11157 Prlr prolactin receptor gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12810576 11157 Prlr prolactin receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11159821 11157 Prlr prolactin receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15388648 11157 Prlr prolactin receptor gene MP:0001346 abnormal lacrimal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11133844 11157 Prlr prolactin receptor gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:9009200 11157 Prlr prolactin receptor gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:9751488 11157 Prlr prolactin receptor gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:9009200 11157 Prlr prolactin receptor gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:15388648 11157 Prlr prolactin receptor gene MP:0001562 abnormal circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:9886812 11157 Prlr prolactin receptor gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:9009200 11157 Prlr prolactin receptor gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:9009200 11157 Prlr prolactin receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12810576 11157 Prlr prolactin receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:9009200 11157 Prlr prolactin receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12810576 11157 Prlr prolactin receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9009200 11157 Prlr prolactin receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9009200 11157 Prlr prolactin receptor gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:9009200 11157 Prlr prolactin receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15388648 11157 Prlr prolactin receptor gene MP:0002832 coarse hair IAGP N RGD:5509061 20141003 MGI PMID:11356702 11157 Prlr prolactin receptor gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:9886812 11157 Prlr prolactin receptor gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:9886812 11157 Prlr prolactin receptor gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:11897695 11157 Prlr prolactin receptor gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:15388648 11157 Prlr prolactin receptor gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:15388648 11157 Prlr prolactin receptor gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20220804 MGI PMID:9009200 11157 Prlr prolactin receptor gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:9009200 11157 Prlr prolactin receptor gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:15388648 11157 Prlr prolactin receptor gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:9009200 11157 Prlr prolactin receptor gene MP:0004015 abnormal oviduct environment IAGP N RGD:5509061 20141003 MGI PMID:9009200 11157 Prlr prolactin receptor gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:9886812 11157 Prlr prolactin receptor gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:15388648 11157 Prlr prolactin receptor gene MP:0004909 increased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:12810576 11157 Prlr prolactin receptor gene MP:0005124 increased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:9886812 11157 Prlr prolactin receptor gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:9886812 11157 Prlr prolactin receptor gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:9886812 11157 Prlr prolactin receptor gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:11897695 11157 Prlr prolactin receptor gene MP:0005248 abnormal Harderian gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11133844 11157 Prlr prolactin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11897695 11157 Prlr prolactin receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15388648 11157 Prlr prolactin receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15388648 11157 Prlr prolactin receptor gene MP:0005471 decreased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:16166330 11157 Prlr prolactin receptor gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:16166330 11157 Prlr prolactin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15388648 11157 Prlr prolactin receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15388648 11157 Prlr prolactin receptor gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11159821 11157 Prlr prolactin receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15388648 11157 Prlr prolactin receptor gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9886812 11157 Prlr prolactin receptor gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11159821 11157 Prlr prolactin receptor gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:15388648 11157 Prlr prolactin receptor gene MP:0008779 abnormal maternal behavior IAGP N RGD:5509061 20141003 MGI PMID:9751488 11157 Prlr prolactin receptor gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:11897695 11157 Prlr prolactin receptor gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:11897695 11157 Prlr prolactin receptor gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:12810576 11157 Prlr prolactin receptor gene MP:0009287 decreased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11159821 11157 Prlr prolactin receptor gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:12511652 11157 Prlr prolactin receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15388648 11157 Prlr prolactin receptor gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16166330 11157 Prlr prolactin receptor gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:9009200 11157 Prlr prolactin receptor gene MP:0011988 increased mating frequency IAGP N RGD:5509061 20240627 MGI PMID:9009200 11157 Prlr prolactin receptor gene MP:0013476 abnormal Harderian gland porphyrin secretion IAGP N RGD:5509061 20150212 MGI PMID:11133844 11157 Prlr prolactin receptor gene MP:0031364 increased prostate gland ventral lobe weight IAGP N RGD:5509061 20220303 MGI PMID:12810576 11158 Prm1 protamine 1 gene MP:0001924 infertility IAGP N RGD:5509061 20180719 MGI PMID:11326282 11158 Prm1 protamine 1 gene MP:0005410 abnormal fertilization IAGP N RGD:5509061 20180719 MGI PMID:11326282 11158 Prm1 protamine 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20180719 MGI PMID:11326282 11158 Prm1 protamine 1 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220714 MGI PMID:11326282 11159 Prm2 protamine 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:11326282 11159 Prm2 protamine 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:12620939 11159 Prm2 protamine 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20220407 MGI PMID:27833122 11159 Prm2 protamine 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20230413 MGI PMID:32727081 11159 Prm2 protamine 2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220407 MGI PMID:27833122 11159 Prm2 protamine 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20230413 MGI PMID:32727081 11159 Prm2 protamine 2 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20220407 MGI PMID:27833122 11159 Prm2 protamine 2 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20230413 MGI PMID:32727081 11159 Prm2 protamine 2 gene MP:0005410 abnormal fertilization IAGP N RGD:5509061 20141003 MGI PMID:11326282 11159 Prm2 protamine 2 gene MP:0005410 abnormal fertilization IAGP N RGD:5509061 20141003 MGI PMID:12620939 11159 Prm2 protamine 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11326282 11159 Prm2 protamine 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12620939 11159 Prm2 protamine 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220407 MGI PMID:27833122 11159 Prm2 protamine 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220407 MGI PMID:27833122 11159 Prm2 protamine 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20230413 MGI PMID:32727081 11159 Prm2 protamine 2 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20220407 MGI PMID:27833122 11159 Prm2 protamine 2 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220407 MGI PMID:27833122 11159 Prm2 protamine 2 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20230413 MGI PMID:32727081 11159 Prm2 protamine 2 gene MP:0009235 small sperm head IAGP N RGD:5509061 20230413 MGI PMID:32727081 11159 Prm2 protamine 2 gene MP:0009325 necrospermia IAGP N RGD:5509061 20230413 MGI PMID:32727081 11159 Prm2 protamine 2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220407 MGI PMID:27833122 11159 Prm2 protamine 2 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220407 MGI PMID:27833122 11159 Prm2 protamine 2 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220714 MGI PMID:11326282 11160 Prnp prion protein gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19038218 11160 Prnp prion protein gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22072968 11160 Prnp prion protein gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:15161660 11160 Prnp prion protein gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:22072968 11160 Prnp prion protein gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17709374 11160 Prnp prion protein gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16517717 11160 Prnp prion protein gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11179214 11160 Prnp prion protein gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15351724 11160 Prnp prion protein gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:22072968 11160 Prnp prion protein gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:22619325 11160 Prnp prion protein gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:22072968 11160 Prnp prion protein gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:8635458 11160 Prnp prion protein gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20190307 MGI PMID:27440899 11160 Prnp prion protein gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:11179214 11160 Prnp prion protein gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19666958 11160 Prnp prion protein gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:8606772 11160 Prnp prion protein gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:11179214 11160 Prnp prion protein gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:11179214 11160 Prnp prion protein gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:19666958 11160 Prnp prion protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19666958 11160 Prnp prion protein gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19666958 11160 Prnp prion protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10525406 11160 Prnp prion protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11179214 11160 Prnp prion protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15351724 11160 Prnp prion protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19038218 11160 Prnp prion protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19675240 11160 Prnp prion protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22619325 11160 Prnp prion protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:8606772 11160 Prnp prion protein gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17270731 11160 Prnp prion protein gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19666958 11160 Prnp prion protein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17270731 11160 Prnp prion protein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19666958 11160 Prnp prion protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:8606772 11160 Prnp prion protein gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19666958 11160 Prnp prion protein gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19675240 11160 Prnp prion protein gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:17270731 11160 Prnp prion protein gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:17270731 11160 Prnp prion protein gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:8035877 11160 Prnp prion protein gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:19038218 11160 Prnp prion protein gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:19666958 11160 Prnp prion protein gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22072968 11160 Prnp prion protein gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22619325 11160 Prnp prion protein gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:19675240 11160 Prnp prion protein gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:19038218 11160 Prnp prion protein gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:17709374 11160 Prnp prion protein gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16517717 11160 Prnp prion protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15007175 11160 Prnp prion protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15161660 11160 Prnp prion protein gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:19666958 11160 Prnp prion protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19038218 11160 Prnp prion protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19675240 11160 Prnp prion protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22072968 11160 Prnp prion protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8698234 11160 Prnp prion protein gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11179214 11160 Prnp prion protein gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:22072968 11160 Prnp prion protein gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16517717 11160 Prnp prion protein gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17709374 11160 Prnp prion protein gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:8698234 11160 Prnp prion protein gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20190307 MGI PMID:27440899 11160 Prnp prion protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11179214 11160 Prnp prion protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16219759 11160 Prnp prion protein gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:15007175 11160 Prnp prion protein gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0002183 gliosis IAGP N RGD:5509061 20160428 MGI PMID:12456643 11160 Prnp prion protein gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:8035877 11160 Prnp prion protein gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:22072968 11160 Prnp prion protein gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:17270731 11160 Prnp prion protein gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:8698234 11160 Prnp prion protein gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20160428 MGI PMID:12456643 11160 Prnp prion protein gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20190307 MGI PMID:27440899 11160 Prnp prion protein gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:19666958 11160 Prnp prion protein gene MP:0002911 abnormal inhibitory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:8035877 11160 Prnp prion protein gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:17270731 11160 Prnp prion protein gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:8035877 11160 Prnp prion protein gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:22072968 11160 Prnp prion protein gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0003314 dysmetria IAGP N RGD:5509061 20141003 MGI PMID:22619325 11160 Prnp prion protein gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:19675240 11160 Prnp prion protein gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:20445063 11160 Prnp prion protein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:20445063 11160 Prnp prion protein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22072968 11160 Prnp prion protein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:8698234 11160 Prnp prion protein gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20141003 MGI PMID:11823413 11160 Prnp prion protein gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:16492732 11160 Prnp prion protein gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:17270731 11160 Prnp prion protein gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:8698234 11160 Prnp prion protein gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:16517717 11160 Prnp prion protein gene MP:0003952 abnormal copper level IAGP N RGD:5509061 20141003 MGI PMID:16517717 11160 Prnp prion protein gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:19666958 11160 Prnp prion protein gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:15161660 11160 Prnp prion protein gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17270731 11160 Prnp prion protein gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16517717 11160 Prnp prion protein gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:16492732 11160 Prnp prion protein gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16517717 11160 Prnp prion protein gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16517717 11160 Prnp prion protein gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:14633630 11160 Prnp prion protein gene MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:15170227 11160 Prnp prion protein gene MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:15354287 11160 Prnp prion protein gene MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:16480953 11160 Prnp prion protein gene MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:17709374 11160 Prnp prion protein gene MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:2890436 11160 Prnp prion protein gene MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:7494265 11160 Prnp prion protein gene MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20200416 MGI PMID:11823413 11160 Prnp prion protein gene MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20200416 MGI PMID:17270731 11160 Prnp prion protein gene MP:0005364 increased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:14633630 11160 Prnp prion protein gene MP:0005364 increased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:16480953 11160 Prnp prion protein gene MP:0005364 increased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:17709374 11160 Prnp prion protein gene MP:0005364 increased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:2890436 11160 Prnp prion protein gene MP:0005364 increased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:8635458 11160 Prnp prion protein gene MP:0005364 increased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:8698234 11160 Prnp prion protein gene MP:0005364 increased susceptibility to prion infection IAGP N RGD:5509061 20160428 MGI PMID:12456643 11160 Prnp prion protein gene MP:0005364 increased susceptibility to prion infection IAGP N RGD:5509061 20190307 MGI PMID:27440899 11160 Prnp prion protein gene MP:0005364 increased susceptibility to prion infection IAGP N RGD:5509061 20200416 MGI PMID:11823413 11160 Prnp prion protein gene MP:0005364 increased susceptibility to prion infection IAGP N RGD:5509061 20200416 MGI PMID:17270731 11160 Prnp prion protein gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15007175 11160 Prnp prion protein gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:19675240 11160 Prnp prion protein gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16517717 11160 Prnp prion protein gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16517717 11160 Prnp prion protein gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16517717 11160 Prnp prion protein gene MP:0008232 abnormal cingulum morphology IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16517717 11160 Prnp prion protein gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:22072968 11160 Prnp prion protein gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11823413 11160 Prnp prion protein gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16492732 11160 Prnp prion protein gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0010072 increased pruritus IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0010132 decreased DN2 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16517717 11160 Prnp prion protein gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16517717 11160 Prnp prion protein gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16517717 11160 Prnp prion protein gene MP:0011149 abnormal hippocampus stratum lacunosum morphology IAGP N RGD:5509061 20141003 MGI PMID:19073920 11160 Prnp prion protein gene MP:0011214 increased brain copper level IAGP N RGD:5509061 20141003 MGI PMID:14511115 11160 Prnp prion protein gene MP:0011215 decreased brain copper level IAGP N RGD:5509061 20141003 MGI PMID:14511115 11160 Prnp prion protein gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:19709627 11160 Prnp prion protein gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:23959875 11160 Prnp prion protein gene MP:0011979 abnormal magnesium ion homeostasis IAGP N RGD:5509061 20161201 MGI PMID:14511115 11160 Prnp prion protein gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:19709627 11160 Prnp prion protein gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:19666958 11160 Prnp prion protein gene MP:0020187 abnormal susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:10581259 11160 Prnp prion protein gene MP:0020187 abnormal susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:9462739 11160 Prnp prion protein gene MP:0021198 abnormal sleep duration IAGP N RGD:5509061 20220922 MGI PMID:23959875 11161 Proc protein C gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9788960 11161 Proc protein C gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10749569 11161 Proc protein C gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:9788960 11161 Proc protein C gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:9788960 11161 Proc protein C gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10749569 11161 Proc protein C gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9788960 11161 Proc protein C gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:10749569 11161 Proc protein C gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0002343 abnormal lymph node cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:9788960 11161 Proc protein C gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:10749569 11161 Proc protein C gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:9788960 11161 Proc protein C gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:9788960 11161 Proc protein C gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9788960 11161 Proc protein C gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:10749569 11161 Proc protein C gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0009275 bruising IAGP N RGD:5509061 20141003 MGI PMID:9788960 11161 Proc protein C gene MP:0010178 increased number of Howell-Jolly bodies IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10749569 11161 Proc protein C gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9788960 11161 Proc protein C gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11159184 11161 Proc protein C gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9788960 11161 Proc protein C gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20201210 MGI PMID:9788960 11161 Proc protein C gene MP:0031051 lymph node hemorrhage IAGP N RGD:5509061 20200618 MGI PMID:11159184 11161 Proc protein C gene MP:0031126 gangrene IAGP N RGD:5509061 20200917 MGI PMID:11159184 11161 Proc protein C gene MP:0031167 abnormal lung thrombosis IAGP N RGD:5509061 20201210 MGI PMID:9788960 11161 Proc protein C gene MP:0031168 abnormal brain thrombosis IAGP N RGD:5509061 20201210 MGI PMID:9788960 11166 Prph peripherin gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12065660 11166 Prph peripherin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:12065660 11168 Prps2 phosphoribosyl pyrophosphate synthetase 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20150827 MGI PMID:24855946 11168 Prps2 phosphoribosyl pyrophosphate synthetase 2 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20150827 MGI PMID:24855946 11168 Prps2 phosphoribosyl pyrophosphate synthetase 2 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20150827 MGI PMID:24855946 11168 Prps2 phosphoribosyl pyrophosphate synthetase 2 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20150827 MGI PMID:24855946 11178 Psap prosaposin gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:17167097 11178 Psap prosaposin gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:17167097 11178 Psap prosaposin gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0000436 abnormal head movements IAGP N RGD:5509061 20141003 MGI PMID:8776585 11178 Psap prosaposin gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:15345707 11178 Psap prosaposin gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15345707 11178 Psap prosaposin gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:18480170 11178 Psap prosaposin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:8776585 11178 Psap prosaposin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0000745 tremors IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:8776585 11178 Psap prosaposin gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:15345707 11178 Psap prosaposin gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15345707 11178 Psap prosaposin gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:11726558 11178 Psap prosaposin gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:8776585 11178 Psap prosaposin gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11105903 11178 Psap prosaposin gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11105903 11178 Psap prosaposin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18480170 11178 Psap prosaposin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8776585 11178 Psap prosaposin gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15345707 11178 Psap prosaposin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18480170 11178 Psap prosaposin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:8776585 11178 Psap prosaposin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18480170 11178 Psap prosaposin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11726558 11178 Psap prosaposin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15345707 11178 Psap prosaposin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:11726558 11178 Psap prosaposin gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:15345707 11178 Psap prosaposin gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:18480170 11178 Psap prosaposin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0001513 limb grasping IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:15345707 11178 Psap prosaposin gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:18480170 11178 Psap prosaposin gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:11726558 11178 Psap prosaposin gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:12810822 11178 Psap prosaposin gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:15345707 11178 Psap prosaposin gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:18480170 11178 Psap prosaposin gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:17167097 11178 Psap prosaposin gene MP:0002059 abnormal seminal vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11105903 11178 Psap prosaposin gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11726558 11178 Psap prosaposin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12810822 11178 Psap prosaposin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15345707 11178 Psap prosaposin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8776585 11178 Psap prosaposin gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:18480170 11178 Psap prosaposin gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:18480170 11178 Psap prosaposin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15743835 11178 Psap prosaposin gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:11105903 11178 Psap prosaposin gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15345707 11178 Psap prosaposin gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:8776585 11178 Psap prosaposin gene MP:0002809 increased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:8776585 11178 Psap prosaposin gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:8776585 11178 Psap prosaposin gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:21700325 11178 Psap prosaposin gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0003382 straub tail IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:11105903 11178 Psap prosaposin gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:11726558 11178 Psap prosaposin gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18480170 11178 Psap prosaposin gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:11726558 11178 Psap prosaposin gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:11105903 11178 Psap prosaposin gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0004302 abnormal Deiters cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17167097 11178 Psap prosaposin gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17167097 11178 Psap prosaposin gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17167097 11178 Psap prosaposin gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17167097 11178 Psap prosaposin gene MP:0004632 abnormal cochlear OHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17167097 11178 Psap prosaposin gene MP:0004633 abnormal cochlear IHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17167097 11178 Psap prosaposin gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:17167097 11178 Psap prosaposin gene MP:0004746 abnormal cochlear IHC afferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17167097 11178 Psap prosaposin gene MP:0004757 abnormal distal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18480170 11178 Psap prosaposin gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11105903 11178 Psap prosaposin gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:11105903 11178 Psap prosaposin gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:11105903 11178 Psap prosaposin gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:11105903 11178 Psap prosaposin gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11105903 11178 Psap prosaposin gene MP:0004962 decreased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:11105903 11178 Psap prosaposin gene MP:0005180 abnormal circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:11105903 11178 Psap prosaposin gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0005302 neurogenic bladder IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:17353235 11178 Psap prosaposin gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:18480170 11178 Psap prosaposin gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:11371512 11178 Psap prosaposin gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:8776585 11178 Psap prosaposin gene MP:0008285 abnormal hippocampus granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18480170 11178 Psap prosaposin gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20141003 MGI PMID:20015957 11178 Psap prosaposin gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20141003 MGI PMID:9678511 11178 Psap prosaposin gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8776585 11178 Psap prosaposin gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8776585 11178 Psap prosaposin gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12810822 11178 Psap prosaposin gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8776585 11178 Psap prosaposin gene MP:0011617 abnormal habituation IAGP N RGD:5509061 20141003 MGI PMID:23446636 11178 Psap prosaposin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17167097 11178 Psap prosaposin gene MP:0014062 nervous system inclusion bodies IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0014409 decreased distortion product otoacoustic emission amplitude IAGP N RGD:5509061 20240405 MGI PMID:17167097 11178 Psap prosaposin gene MP:0020261 increased beta-galactosidase level IAGP N RGD:5509061 20200806 MGI PMID:20175216 11178 Psap prosaposin gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20190711 MGI PMID:23446636 11180 Psmb9 proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2) gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:7600282 11180 Psmb9 proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2) gene MP:0001836 abnormal antigen presentation via MHC class I IAGP N RGD:5509061 20141003 MGI PMID:22197977 11180 Psmb9 proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2) gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:22197977 11180 Psmb9 proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2) gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11169961 11180 Psmb9 proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2) gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11169961 11180 Psmb9 proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2) gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11782352 11180 Psmb9 proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2) gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7600282 11180 Psmb9 proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2) gene MP:0002453 abnormal B lymphocyte antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:22197977 11180 Psmb9 proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2) gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:22197977 11180 Psmb9 proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2) gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11782352 11180 Psmb9 proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2) gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11782352 11180 Psmb9 proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22197977 11180 Psmb9 proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:7600282 11180 Psmb9 proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2) gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11169961 11180 Psmb9 proteasome (prosome, macropain) subunit, beta type 9 (large multifunctional peptidase 2) gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:7600282 11181 Pspn persephin gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:12093930 11181 Pspn persephin gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:12093930 11182 Ptgds prostaglandin D2 synthase (brain) gene MP:0000362 decreased mast cell histamine storage IAGP N RGD:5509061 20141003 MGI PMID:23624557 11182 Ptgds prostaglandin D2 synthase (brain) gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20211118 MGI PMID:33972431 11182 Ptgds prostaglandin D2 synthase (brain) gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23624557 11182 Ptgds prostaglandin D2 synthase (brain) gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:9892701 11182 Ptgds prostaglandin D2 synthase (brain) gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21242963 11182 Ptgds prostaglandin D2 synthase (brain) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21242963 11182 Ptgds prostaglandin D2 synthase (brain) gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17283118 11182 Ptgds prostaglandin D2 synthase (brain) gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21242963 11182 Ptgds prostaglandin D2 synthase (brain) gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23624557 11182 Ptgds prostaglandin D2 synthase (brain) gene MP:0008020 abnormal dermal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23624557 11182 Ptgds prostaglandin D2 synthase (brain) gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:23624557 11182 Ptgds prostaglandin D2 synthase (brain) gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20211118 MGI PMID:33972431 11182 Ptgds prostaglandin D2 synthase (brain) gene MP:0010281 increased nervous system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21242963 11182 Ptgds prostaglandin D2 synthase (brain) gene MP:0010311 increased meningioma incidence IAGP N RGD:5509061 20141003 MGI PMID:21242963 11182 Ptgds prostaglandin D2 synthase (brain) gene MP:0010313 increased osteoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21242963 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0000532 kidney vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210128 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0002833 increased heart weight IEA N RGD:5509061 20201022 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0002989 small kidney IEA N RGD:5509061 20210128 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0003670 dilated renal glomerular capsule IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0003918 decreased kidney weight IEA N RGD:5509061 20201022 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0003946 renal necrosis IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0005238 increased brain size IEA N RGD:5509061 20210128 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210128 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0009818 abnormal thromboxane level IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0009871 abnormal aorta tunica adventitia morphology IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0010468 abnormal thoracic aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12403673 11183 Ptgis prostaglandin I2 (prostacyclin) synthase gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20141003 MGI PMID:12403673 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:15883230 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:15699263 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17219415 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20230601 MGI 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0000505 decreased digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:15542509 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10683376 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0001422 abnormal drinking behavior IAGP N RGD:5509061 20141003 MGI PMID:12183660 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11158594 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15776109 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:8521478 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11158594 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:16556900 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:11052981 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10987272 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17110378 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10987272 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:8521478 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:8521478 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:14630706 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:9751758 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:16556900 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20141003 MGI PMID:9751758 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:10944235 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:11158594 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16732282 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0003177 allodynia IAGP N RGD:5509061 20141003 MGI PMID:16556900 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:16556900 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:12183660 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:18833324 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:8521478 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:19056763 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:11705824 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230601 MGI 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:11052981 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15883230 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:12118094 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:10683376 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:9751758 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0005527 increased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:15883230 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0005531 increased renal vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:15883230 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:15776109 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15699263 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0008004 abnormal stomach pH IAGP N RGD:5509061 20141003 MGI PMID:15542509 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:10987272 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:10683376 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20061361 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:11832369 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11052981 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11282894 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15542509 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15699263 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19056763 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20230601 MGI 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20200917 MGI PMID:15776109 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20200917 MGI PMID:8521478 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15883230 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10683376 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:11444591 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:10683376 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:10987272 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:11052981 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:11705824 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:14630706 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:15699263 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:16204198 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:17219415 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:8521478 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:9751758 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0009818 abnormal thromboxane level IAGP N RGD:5509061 20141003 MGI PMID:16614756 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:9751758 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0011021 abnormal circadian regulation of heart rate IAGP N RGD:5509061 20141003 MGI PMID:15883230 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0011022 abnormal circadian regulation of systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15883230 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11158594 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10944235 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16732282 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11158594 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10944235 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0011564 decreased urine prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:15883230 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0011564 decreased urine prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:16614756 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0012008 delayed parturition IAGP N RGD:5509061 20141003 MGI PMID:10944235 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0012008 delayed parturition IAGP N RGD:5509061 20141003 MGI PMID:11158594 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0012008 delayed parturition IAGP N RGD:5509061 20141003 MGI PMID:18833324 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0012008 delayed parturition IAGP N RGD:5509061 20191219 MGI PMID:9751758 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0012009 early parturition IAGP N RGD:5509061 20191219 MGI PMID:18833324 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0012124 increased bronchoconstrictive response IAGP N RGD:5509061 20141003 MGI PMID:18753249 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:15776109 11184 Ptgs1 prostaglandin-endoperoxide synthase 1 gene MP:0031180 decreased brain blood flow rate IAGP N RGD:5509061 20201119 MGI PMID:11282894 11186 Pth parathyroid hormone gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20211021 MGI 11186 Pth parathyroid hormone gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20201022 MGI 11186 Pth parathyroid hormone gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 11186 Pth parathyroid hormone gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0003112 enlarged parathyroid gland IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0004635 short metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0004670 small vertebral body IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20171221 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0030441 increased osteoblast apoptosis IAGP N RGD:5509061 20171221 MGI PMID:11994406 11186 Pth parathyroid hormone gene MP:0030479 increased osteocyte apoptosis IAGP N RGD:5509061 20171221 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16138191 11188 Pthlh parathyroid hormone-like peptide gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:11316774 11188 Pthlh parathyroid hormone-like peptide gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:11760831 11188 Pthlh parathyroid hormone-like peptide gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:9391087 11188 Pthlh parathyroid hormone-like peptide gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:11792564 11188 Pthlh parathyroid hormone-like peptide gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:9391087 11188 Pthlh parathyroid hormone-like peptide gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11760831 11188 Pthlh parathyroid hormone-like peptide gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16138191 11188 Pthlh parathyroid hormone-like peptide gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:14751559 11188 Pthlh parathyroid hormone-like peptide gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15951842 11188 Pthlh parathyroid hormone-like peptide gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0000168 abnormal bone marrow development IAGP N RGD:5509061 20141003 MGI PMID:15951842 11188 Pthlh parathyroid hormone-like peptide gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20170105 MGI 11188 Pthlh parathyroid hormone-like peptide gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20141003 MGI 11188 Pthlh parathyroid hormone-like peptide gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:11316774 11188 Pthlh parathyroid hormone-like peptide gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:11760831 11188 Pthlh parathyroid hormone-like peptide gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:14751559 11188 Pthlh parathyroid hormone-like peptide gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:9391087 11188 Pthlh parathyroid hormone-like peptide gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:11760831 11188 Pthlh parathyroid hormone-like peptide gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0000447 flattened snout IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:11760831 11188 Pthlh parathyroid hormone-like peptide gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:14751559 11188 Pthlh parathyroid hormone-like peptide gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20180830 MGI 11188 Pthlh parathyroid hormone-like peptide gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20180830 MGI 11188 Pthlh parathyroid hormone-like peptide gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:11316774 11188 Pthlh parathyroid hormone-like peptide gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0001562 abnormal circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:8938591 11188 Pthlh parathyroid hormone-like peptide gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:9391087 11188 Pthlh parathyroid hormone-like peptide gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11316774 11188 Pthlh parathyroid hormone-like peptide gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9391087 11188 Pthlh parathyroid hormone-like peptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:9391087 11188 Pthlh parathyroid hormone-like peptide gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:14751559 11188 Pthlh parathyroid hormone-like peptide gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20180830 MGI 11188 Pthlh parathyroid hormone-like peptide gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:9391087 11188 Pthlh parathyroid hormone-like peptide gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:16355280 11188 Pthlh parathyroid hormone-like peptide gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:15951842 11188 Pthlh parathyroid hormone-like peptide gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11316774 11188 Pthlh parathyroid hormone-like peptide gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:14751559 11188 Pthlh parathyroid hormone-like peptide gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:15951842 11188 Pthlh parathyroid hormone-like peptide gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9391087 11188 Pthlh parathyroid hormone-like peptide gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:14751559 11188 Pthlh parathyroid hormone-like peptide gene MP:0003112 enlarged parathyroid gland IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:14751559 11188 Pthlh parathyroid hormone-like peptide gene MP:0003416 premature bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9391087 11188 Pthlh parathyroid hormone-like peptide gene MP:0003417 premature endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11316774 11188 Pthlh parathyroid hormone-like peptide gene MP:0003417 premature endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:11316774 11188 Pthlh parathyroid hormone-like peptide gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:16355280 11188 Pthlh parathyroid hormone-like peptide gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9391087 11188 Pthlh parathyroid hormone-like peptide gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8938591 11188 Pthlh parathyroid hormone-like peptide gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:14751559 11188 Pthlh parathyroid hormone-like peptide gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:14751559 11188 Pthlh parathyroid hormone-like peptide gene MP:0004357 long tibia IAGP N RGD:5509061 20141003 MGI PMID:15951842 11188 Pthlh parathyroid hormone-like peptide gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:14751559 11188 Pthlh parathyroid hormone-like peptide gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:14751559 11188 Pthlh parathyroid hormone-like peptide gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:16355280 11188 Pthlh parathyroid hormone-like peptide gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0004673 splayed ribs IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:9391087 11188 Pthlh parathyroid hormone-like peptide gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:11316774 11188 Pthlh parathyroid hormone-like peptide gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0004950 abnormal brain vasculature morphology IEA N RGD:5509061 20180830 MGI 11188 Pthlh parathyroid hormone-like peptide gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:14597768 11188 Pthlh parathyroid hormone-like peptide gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:16138191 11188 Pthlh parathyroid hormone-like peptide gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:16138191 11188 Pthlh parathyroid hormone-like peptide gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:11760831 11188 Pthlh parathyroid hormone-like peptide gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:16138191 11188 Pthlh parathyroid hormone-like peptide gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:16138191 11188 Pthlh parathyroid hormone-like peptide gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11760831 11188 Pthlh parathyroid hormone-like peptide gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:14597768 11188 Pthlh parathyroid hormone-like peptide gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 11188 Pthlh parathyroid hormone-like peptide gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:14597768 11188 Pthlh parathyroid hormone-like peptide gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20180830 MGI 11188 Pthlh parathyroid hormone-like peptide gene MP:0006213 shallow orbits IAGP N RGD:5509061 20171019 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:14751559 11188 Pthlh parathyroid hormone-like peptide gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:15951842 11188 Pthlh parathyroid hormone-like peptide gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:9391087 11188 Pthlh parathyroid hormone-like peptide gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:11316774 11188 Pthlh parathyroid hormone-like peptide gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:14597768 11188 Pthlh parathyroid hormone-like peptide gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15951842 11188 Pthlh parathyroid hormone-like peptide gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16138191 11188 Pthlh parathyroid hormone-like peptide gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:16138191 11188 Pthlh parathyroid hormone-like peptide gene MP:0008922 abnormal cervical rib IEA N RGD:5509061 20180830 MGI 11188 Pthlh parathyroid hormone-like peptide gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14597768 11188 Pthlh parathyroid hormone-like peptide gene MP:0009908 protruding tongue IAGP N RGD:5509061 20141003 MGI PMID:11316774 11188 Pthlh parathyroid hormone-like peptide gene MP:0009908 protruding tongue IAGP N RGD:5509061 20141003 MGI PMID:11760831 11188 Pthlh parathyroid hormone-like peptide gene MP:0009908 protruding tongue IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0010817 absent type I pneumocytes IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0010827 small lung saccule IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0010890 decreased alveolar lamellar body number IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0010898 abnormal pulmonary alveolus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11316774 11188 Pthlh parathyroid hormone-like peptide gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14751559 11188 Pthlh parathyroid hormone-like peptide gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8314082 11188 Pthlh parathyroid hormone-like peptide gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11188 Pthlh parathyroid hormone-like peptide gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0011145 abnormal mesenchymal cell differentiation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:15162506 11188 Pthlh parathyroid hormone-like peptide gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:14597768 11188 Pthlh parathyroid hormone-like peptide gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20180830 MGI 11188 Pthlh parathyroid hormone-like peptide gene MP:0014018 embryo tumor IEA N RGD:5509061 20180830 MGI 11188 Pthlh parathyroid hormone-like peptide gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:19091948 11188 Pthlh parathyroid hormone-like peptide gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20171221 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:15951842 11188 Pthlh parathyroid hormone-like peptide gene MP:0030082 long lower incisors IAGP N RGD:5509061 20170928 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0030262 frontal bossing IAGP N RGD:5509061 20171026 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0030441 increased osteoblast apoptosis IAGP N RGD:5509061 20171221 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0030449 tooth ankylosis IAGP N RGD:5509061 20171221 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0030453 abnormal odontoblast morphology IAGP N RGD:5509061 20180215 MGI PMID:9391087 11188 Pthlh parathyroid hormone-like peptide gene MP:0030479 increased osteocyte apoptosis IAGP N RGD:5509061 20171221 MGI PMID:11994406 11188 Pthlh parathyroid hormone-like peptide gene MP:0030495 absent tooth root IAGP N RGD:5509061 20191219 MGI PMID:9751753 11188 Pthlh parathyroid hormone-like peptide gene MP:0030505 tooth impaction IAGP N RGD:5509061 20191219 MGI PMID:9751753 11190 Ptn pleiotrophin gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0001127 small ovary IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0001140 abnormal vagina epithelium morphology IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0001142 abnormal vagina orifice morphology IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0001143 constricted vagina orifice IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:15482347 11190 Ptn pleiotrophin gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16619002 11190 Ptn pleiotrophin gene MP:0001926 female infertility IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:16619002 11190 Ptn pleiotrophin gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:11414790 11190 Ptn pleiotrophin gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11414790 11190 Ptn pleiotrophin gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:15482347 11190 Ptn pleiotrophin gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15482347 11190 Ptn pleiotrophin gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:15482347 11190 Ptn pleiotrophin gene MP:0004895 vagina atrophy IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:15482347 11190 Ptn pleiotrophin gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0009014 prolonged proestrus IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0009018 short estrus IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0009708 vaginal septum IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20220120 MGI PMID:17121547 11190 Ptn pleiotrophin gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:17121547 11192 Ptprg protein tyrosine phosphatase receptor type G gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23029056 11192 Ptprg protein tyrosine phosphatase receptor type G gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16782895 11192 Ptprg protein tyrosine phosphatase receptor type G gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16782895 11192 Ptprg protein tyrosine phosphatase receptor type G gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:16782895 11192 Ptprg protein tyrosine phosphatase receptor type G gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20141003 MGI PMID:16782895 11192 Ptprg protein tyrosine phosphatase receptor type G gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:16782895 11192 Ptprg protein tyrosine phosphatase receptor type G gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:23029056 11194 Ptpra protein tyrosine phosphatase receptor type A gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12932834 11194 Ptpra protein tyrosine phosphatase receptor type A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12932834 11194 Ptpra protein tyrosine phosphatase receptor type A gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12932834 11194 Ptpra protein tyrosine phosphatase receptor type A gene MP:0001488 increased startle reflex IEA N RGD:5509061 20181227 MGI 11194 Ptpra protein tyrosine phosphatase receptor type A gene MP:0002068 abnormal parental behavior IAGP N RGD:5509061 20141003 MGI PMID:10339427 11194 Ptpra protein tyrosine phosphatase receptor type A gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:10339427 11194 Ptpra protein tyrosine phosphatase receptor type A gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12932834 11194 Ptpra protein tyrosine phosphatase receptor type A gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:10339427 11194 Ptpra protein tyrosine phosphatase receptor type A gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20210429 MGI PMID:32491951 11194 Ptpra protein tyrosine phosphatase receptor type A gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 11194 Ptpra protein tyrosine phosphatase receptor type A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10339427 11194 Ptpra protein tyrosine phosphatase receptor type A gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20201022 MGI 11194 Ptpra protein tyrosine phosphatase receptor type A gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18046458 11194 Ptpra protein tyrosine phosphatase receptor type A gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:18779349 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20150129 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20151119 MGI PMID:22724066 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10508267 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8666928 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10970857 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8334701 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8666928 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20151203 MGI PMID:24068938 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15823427 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15823427 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:18779349 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20151203 MGI PMID:24068938 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20150129 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10508267 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20346773 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20346773 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10970857 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10508267 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20346773 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22988576 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8666928 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9725213 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10508267 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18779349 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8666928 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10508267 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:8666928 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002492 decreased IgE level IEA N RGD:5509061 20190418 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002619 abnormal lymphocyte morphology IEA N RGD:5509061 20190411 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15867094 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:8334701 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0004917 abnormal T cell selection IEA N RGD:5509061 20111116 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:10508267 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20150129 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:18779349 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IEA N RGD:5509061 20190418 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20151119 MGI PMID:22724066 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8334701 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8666928 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20151119 MGI PMID:22724066 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:8334701 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:10508267 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:8334701 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:9725213 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:10508267 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:8334701 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:8666928 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20151203 MGI PMID:24068938 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10508267 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20346773 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8666928 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8334701 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8334701 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:8046327 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20151203 MGI PMID:24068938 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0006264 decreased systemic arterial systolic blood pressure IEA N RGD:5509061 20190411 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9725213 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008037 abnormal T cell morphology IEA N RGD:5509061 20111116 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20190103 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:15867094 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20190411 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008048 abnormal memory T cell number IEA N RGD:5509061 20111116 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008050 decreased memory T cell number IEA N RGD:5509061 20150129 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008070 absent T cells IEA N RGD:5509061 20111116 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10508267 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20346773 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8334701 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8666928 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20151203 MGI PMID:24068938 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190411 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10508267 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8334701 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8666928 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20151203 MGI PMID:24068938 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008082 increased single-positive T cell number IEA N RGD:5509061 20150129 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008083 decreased single-positive T cell number IEA N RGD:5509061 20150129 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008126 increased dendritic cell number IEA N RGD:5509061 20150129 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008168 decreased B-1a cell number IEA N RGD:5509061 20150129 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20150129 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008170 decreased B-1b cell number IEA N RGD:5509061 20181011 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008172 abnormal follicular B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008188 abnormal transitional stage B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008191 abnormal follicular B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20150129 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:19299707 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008246 abnormal leukocyte morphology IEA N RGD:5509061 20111116 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:9725213 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008400 abnormal CD4-positive, alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9725213 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008524 increased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:11163182 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15867094 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008729 decreased memory B cell number IEA N RGD:5509061 20150129 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20180329 MGI PMID:29440507 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:8046327 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008894 abnormal intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9725213 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0008895 abnormal intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:9725213 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0009785 abnormal susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20180329 MGI PMID:29440507 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:15823427 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20151203 MGI PMID:24068938 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20151203 MGI PMID:24068938 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15867094 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16627620 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20180329 MGI PMID:29440507 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0010836 decreased CD4-positive, alpha-beta memory T cell number IEA N RGD:5509061 20150129 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0010839 decreased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20150129 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181004 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181004 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0010845 decreased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190613 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20181004 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0010848 decreased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20190613 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181004 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10508267 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20181004 MGI 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:18249142 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:24068938 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:29440507 11196 Ptprc protein tyrosine phosphatase receptor type C gene MP:0031045 decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:29440507 11199 Pvalb parvalbumin gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200604 MGI PMID:28442491 11199 Pvalb parvalbumin gene MP:0000231 hypertension IAGP N RGD:5509061 20200604 MGI PMID:28442491 11199 Pvalb parvalbumin gene MP:0000436 abnormal head movements IAGP N RGD:5509061 20170105 MGI PMID:27131348 11199 Pvalb parvalbumin gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16860487 11199 Pvalb parvalbumin gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15836427 11199 Pvalb parvalbumin gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20160407 MGI PMID:25116249 11199 Pvalb parvalbumin gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160304 MGI PMID:26590342 11199 Pvalb parvalbumin gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20150122 MGI PMID:24430185 11199 Pvalb parvalbumin gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20170105 MGI PMID:27131348 11199 Pvalb parvalbumin gene MP:0001393 ataxia IAGP N RGD:5509061 20160304 MGI PMID:26590342 11199 Pvalb parvalbumin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20150917 MGI PMID:24995986 11199 Pvalb parvalbumin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160304 MGI PMID:26590342 11199 Pvalb parvalbumin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160407 MGI PMID:25116249 11199 Pvalb parvalbumin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160304 MGI PMID:26590342 11199 Pvalb parvalbumin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20230330 MGI PMID:36828548 11199 Pvalb parvalbumin gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20170105 MGI PMID:27131348 11199 Pvalb parvalbumin gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20170105 MGI PMID:27131348 11199 Pvalb parvalbumin gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20170105 MGI PMID:27131348 11199 Pvalb parvalbumin gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20160304 MGI PMID:26590342 11199 Pvalb parvalbumin gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20150122 MGI PMID:24430185 11199 Pvalb parvalbumin gene MP:0002083 premature death IAGP N RGD:5509061 20160304 MGI PMID:26590342 11199 Pvalb parvalbumin gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20200604 MGI PMID:28442491 11199 Pvalb parvalbumin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20023653 11199 Pvalb parvalbumin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20231123 MGI PMID:27618674 11199 Pvalb parvalbumin gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20150122 MGI PMID:24430185 11199 Pvalb parvalbumin gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20150122 MGI PMID:24430185 11199 Pvalb parvalbumin gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20170105 MGI PMID:27131348 11199 Pvalb parvalbumin gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20230330 MGI PMID:36828548 11199 Pvalb parvalbumin gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22378872 11199 Pvalb parvalbumin gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20200604 MGI PMID:28442491 11199 Pvalb parvalbumin gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20200604 MGI PMID:28442491 11199 Pvalb parvalbumin gene MP:0004167 abnormal cingulate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:23671099 11199 Pvalb parvalbumin gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20200604 MGI PMID:28442491 11199 Pvalb parvalbumin gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20170105 MGI PMID:27131348 11199 Pvalb parvalbumin gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20190620 MGI PMID:27253061 11199 Pvalb parvalbumin gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20230330 MGI PMID:36828548 11199 Pvalb parvalbumin gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20200604 MGI PMID:28442491 11199 Pvalb parvalbumin gene MP:0005583 decreased renin activity IAGP N RGD:5509061 20200604 MGI PMID:28442491 11199 Pvalb parvalbumin gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20200604 MGI PMID:28442491 11199 Pvalb parvalbumin gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9950767 11199 Pvalb parvalbumin gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:16860487 11199 Pvalb parvalbumin gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:22378872 11199 Pvalb parvalbumin gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20160304 MGI PMID:26590342 11199 Pvalb parvalbumin gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20170105 MGI PMID:27131348 11199 Pvalb parvalbumin gene MP:0012318 slow extinction of fear memory IAGP N RGD:5509061 20170105 MGI PMID:27131348 11199 Pvalb parvalbumin gene MP:0012339 hyperkalemia IAGP N RGD:5509061 20200604 MGI PMID:28442491 11199 Pvalb parvalbumin gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20200604 MGI PMID:28442491 11199 Pvalb parvalbumin gene MP:0014331 abnormal Purkinje cell mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:16860487 11199 Pvalb parvalbumin gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:27131348 11199 Pvalb parvalbumin gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20170105 MGI PMID:27131348 11199 Pvalb parvalbumin gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22378872 11204 Slc39a7 solute carrier family 39 (zinc transporter), member 7 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20170629 MGI PMID:27736879 11204 Slc39a7 solute carrier family 39 (zinc transporter), member 7 gene MP:0002083 premature death IAGP N RGD:5509061 20170629 MGI PMID:27736879 11204 Slc39a7 solute carrier family 39 (zinc transporter), member 7 gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20170629 MGI PMID:27736879 11204 Slc39a7 solute carrier family 39 (zinc transporter), member 7 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20170629 MGI PMID:27736879 11204 Slc39a7 solute carrier family 39 (zinc transporter), member 7 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20170629 MGI PMID:27736879 11204 Slc39a7 solute carrier family 39 (zinc transporter), member 7 gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20170629 MGI PMID:27736879 11204 Slc39a7 solute carrier family 39 (zinc transporter), member 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 11204 Slc39a7 solute carrier family 39 (zinc transporter), member 7 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20231207 MGI 11204 Slc39a7 solute carrier family 39 (zinc transporter), member 7 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20231207 MGI 11204 Slc39a7 solute carrier family 39 (zinc transporter), member 7 gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20170629 MGI PMID:27736879 11205 H2-M3 histocompatibility 2, M region locus 3 gene MP:0001830 decreased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:16476767 11205 H2-M3 histocompatibility 2, M region locus 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16476767 11205 H2-M3 histocompatibility 2, M region locus 3 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:16476767 11205 H2-M3 histocompatibility 2, M region locus 3 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16476767 11205 H2-M3 histocompatibility 2, M region locus 3 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:16476767 11205 H2-M3 histocompatibility 2, M region locus 3 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16476767 11205 H2-M3 histocompatibility 2, M region locus 3 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16476767 11205 H2-M3 histocompatibility 2, M region locus 3 gene MP:0011077 decreased macrophage nitric oxide production IAGP N RGD:5509061 20141003 MGI PMID:16476767 11210 Art2a ADP-ribosyltransferase 2a gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9300695 11210 Art2a ADP-ribosyltransferase 2a gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:16585549 11210 Art2a ADP-ribosyltransferase 2a gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16585549 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15269275 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:15269275 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15269275 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:15269275 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15269275 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15269275 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15269275 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:16436611 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15269275 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16436611 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:7911226 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:16436611 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:15269275 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:15269275 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15269275 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15269275 11212 Rab3a RAB3A, member RAS oncogene family gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:12244319 11213 Rab4a RAB4A, member RAS oncogene family gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 11213 Rab4a RAB4A, member RAS oncogene family gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210128 MGI 11213 Rab4a RAB4A, member RAS oncogene family gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210128 MGI 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20150910 MGI PMID:18952847 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:16527894 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15467832 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20150910 MGI PMID:18952847 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18922468 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21514245 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000380 small hair follicles IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000447 flattened snout IAGP N RGD:5509061 20171019 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20150910 MGI PMID:18952847 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11296227 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20150910 MGI PMID:18952847 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20150910 MGI PMID:18952847 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17396120 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17396120 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11296227 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20170105 MGI 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001304 cataract IEA N RGD:5509061 20170105 MGI 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11296227 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11296227 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11296227 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:11296227 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11296227 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:11296227 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:11296227 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11296227 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17396120 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11296227 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11296227 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21514245 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11296227 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17396120 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21514245 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:17396120 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20150910 MGI PMID:18952847 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:15467832 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15467832 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20150910 MGI PMID:18952847 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15467832 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15467832 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:17396120 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0003820 increased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18922468 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15467832 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11157055 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16527894 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0006207 embryonic lethality during organogenesis IEA N RGD:5509061 20111116 MGI 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0008526 decreased cranium width IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0008727 increased heart right atrium size IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:18922468 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23453624 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0010031 abnormal cranium size IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0010283 decreased classified tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21514245 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20150910 MGI PMID:18952847 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0010583 abnormal conotruncus morphology IAGP N RGD:5509061 20150910 MGI PMID:18952847 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17396120 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16432225 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17396120 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18922468 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20150910 MGI PMID:18952847 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:21339642 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:22826437 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0012244 increased hepatoblast apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:11296228 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:18922468 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:9767153 11215 Raf1 v-raf-leukemia viral oncogene 1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15467832 11216 Rara retinoic acid receptor, alpha gene MP:0000044 absent organ of Corti IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000075 absent neurocranium IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000099 absent vomer bone IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000111 cleft palate IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000154 rib fusion IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0000161 scoliosis IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0000435 shortened head IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000445 short snout IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:10021334 11216 Rara retinoic acid receptor, alpha gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0000553 absent radius IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000562 polydactyly IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000565 oligodactyly IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:8394014 11216 Rara retinoic acid receptor, alpha gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000914 exencephaly IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000929 open neural tube IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0000935 abnormal folding of telencephalic vesicles IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0001070 abnormal abducens nerve morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:11857786 11216 Rara retinoic acid receptor, alpha gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:8394014 11216 Rara retinoic acid receptor, alpha gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:8394014 11216 Rara retinoic acid receptor, alpha gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:8394014 11216 Rara retinoic acid receptor, alpha gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0001310 abnormal conjunctiva morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8394014 11216 Rara retinoic acid receptor, alpha gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11857786 11216 Rara retinoic acid receptor, alpha gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15901285 11216 Rara retinoic acid receptor, alpha gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8394014 11216 Rara retinoic acid receptor, alpha gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15901285 11216 Rara retinoic acid receptor, alpha gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8394014 11216 Rara retinoic acid receptor, alpha gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7679509 11216 Rara retinoic acid receptor, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8394014 11216 Rara retinoic acid receptor, alpha gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0002257 abnormal arytenoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0002257 abnormal arytenoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0002265 abnormal left major bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0002266 abnormal right major bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20150122 MGI PMID:24458645 11216 Rara retinoic acid receptor, alpha gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15901285 11216 Rara retinoic acid receptor, alpha gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8394014 11216 Rara retinoic acid receptor, alpha gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0002765 short fibula IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:10021334 11216 Rara retinoic acid receptor, alpha gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0003078 aphakia IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0003146 absent cochlear ganglion IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0003558 absent uterus IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0003558 absent uterus IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0003575 absent oviduct IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0003575 absent oviduct IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0003600 ectopic kidney IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18026104 11216 Rara retinoic acid receptor, alpha gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0004358 bowed tibia IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0004380 short frontal bone IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0004550 short trachea IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0004553 absent tracheal cartilage rings IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0004666 absent stapedial artery IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0004666 absent stapedial artery IAGP N RGD:5509061 20170921 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0004790 absent upper incisors IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10021334 11216 Rara retinoic acid receptor, alpha gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15901285 11216 Rara retinoic acid receptor, alpha gene MP:0005579 absent outer ear IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0005623 abnormal meninges morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0006063 abnormal inferior vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0006289 otic capsule hypoplasia IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:15901285 11216 Rara retinoic acid receptor, alpha gene MP:0006425 absent Mullerian ducts IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0006425 absent Mullerian ducts IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15901285 11216 Rara retinoic acid receptor, alpha gene MP:0008380 abnormal gonial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0008823 abnormal interventricular septum membranous part morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0008881 absent Harderian gland IAGP N RGD:5509061 20150205 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0008881 absent Harderian gland IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0009054 absent anal canal IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0009054 absent anal canal IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0009072 absent cranial vagina IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0009072 absent cranial vagina IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0009075 rudimentary Wolffian ducts IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0009076 rudimentary Mullerian ducts IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0009438 cricoid and tracheal cartilage fusion IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0009525 abnormal submandibular duct morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0009526 absent sublingual gland IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0009527 abnormal sublingual duct morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0009569 abnormal left lung morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0009570 abnormal right lung morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0009571 abnormal right lung accessory lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0010146 umbilical hernia IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0010502 ventricle myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0010565 absent fetal ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0010572 persistent right dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0010584 abnormal conotruncus septation IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0010595 abnormal aortic valve cusp morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0010701 fusion of atlas and odontoid process IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0010702 split cervical atlas IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0010703 split cervical axis IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0010709 absent eye anterior chamber IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0010712 absent nasolacrimal duct IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0010713 corneal-lenticular stalk IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0010715 retina coloboma IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0010717 optic nerve coloboma IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0010720 absent sublingual duct IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0010721 short sublingual duct IAGP N RGD:5509061 20171207 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0010721 short sublingual duct IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0010722 persistent cervical thymus IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0010722 persistent cervical thymus IAGP N RGD:5509061 20171207 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0010772 abnormal pollex morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0010980 ectopic ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:10021334 11216 Rara retinoic acid receptor, alpha gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0010987 abnormal nephrogenic mesenchyme morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10021334 11216 Rara retinoic acid receptor, alpha gene MP:0010989 fused bronchial cartilage rings IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8394014 11216 Rara retinoic acid receptor, alpha gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:10021334 11216 Rara retinoic acid receptor, alpha gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0011306 absent kidney pelvis IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0011407 absent nephrogenic zone IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0011486 ectopic ureter IAGP N RGD:5509061 20141003 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0011486 ectopic ureter IAGP N RGD:5509061 20141003 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0012141 absent hindbrain IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0012247 absent cornea IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0012523 abnormal upper lip morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0013233 ectopic thyroid gland IAGP N RGD:5509061 20150122 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0013331 abnormal lacrimal gland development IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0013439 abnormal Harderian gland development IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0013574 ectopic parathyroid gland IAGP N RGD:5509061 20150305 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0013744 abnormal conjunctival sac morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0013826 absent hypoglossal canal IAGP N RGD:5509061 20171026 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0030137 abnormal upper incisor morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0030200 abnormal nasal septum cartilage morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0030304 abnormal cribriform plate morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0030394 abnormal incus short process morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11216 Rara retinoic acid receptor, alpha gene MP:0030406 absent stapes obturator foramen IAGP N RGD:5509061 20171207 MGI PMID:9240560 11216 Rara retinoic acid receptor, alpha gene MP:0030416 absent temporal bone zygomatic process IAGP N RGD:5509061 20171214 MGI PMID:9376317 11216 Rara retinoic acid receptor, alpha gene MP:0030867 small thyroid cartilage IAGP N RGD:5509061 20181101 MGI PMID:7607068 11216 Rara retinoic acid receptor, alpha gene MP:0031445 midline cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:10021334 11217 Rarb retinoic acid receptor, beta gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:11074013 11217 Rarb retinoic acid receptor, beta gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:15635054 11217 Rarb retinoic acid receptor, beta gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15635054 11217 Rarb retinoic acid receptor, beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:16207763 11217 Rarb retinoic acid receptor, beta gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:9883728 11217 Rarb retinoic acid receptor, beta gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:9883728 11217 Rarb retinoic acid receptor, beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:9883728 11217 Rarb retinoic acid receptor, beta gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7958449 11217 Rarb retinoic acid receptor, beta gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0002257 abnormal arytenoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0002265 abnormal left major bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0002266 abnormal right major bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0002271 abnormal pulmonary alveolar duct morphology IAGP N RGD:5509061 20141003 MGI PMID:15635054 11217 Rarb retinoic acid receptor, beta gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20141003 MGI PMID:15635054 11217 Rarb retinoic acid receptor, beta gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0002765 short fibula IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:9883728 11217 Rarb retinoic acid receptor, beta gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:10021334 11217 Rarb retinoic acid receptor, beta gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0003182 decreased pulmonary endothelial cell surface IAGP N RGD:5509061 20141003 MGI PMID:15635054 11217 Rarb retinoic acid receptor, beta gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0003558 absent uterus IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0003558 absent uterus IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0003575 absent oviduct IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0003575 absent oviduct IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0003600 ectopic kidney IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:9376317 11217 Rarb retinoic acid receptor, beta gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0004666 absent stapedial artery IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10021334 11217 Rarb retinoic acid receptor, beta gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0005208 abnormal iris stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:15635054 11217 Rarb retinoic acid receptor, beta gene MP:0006063 abnormal inferior vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0006200 vitreous body deposition IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0006425 absent Mullerian ducts IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0006425 absent Mullerian ducts IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0008380 abnormal gonial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0008514 absent retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0008823 abnormal interventricular septum membranous part morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0008881 absent Harderian gland IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0008972 ethmoturbinate hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0009054 absent anal canal IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0009054 absent anal canal IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0009072 absent cranial vagina IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0009072 absent cranial vagina IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0009076 rudimentary Mullerian ducts IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0009438 cricoid and tracheal cartilage fusion IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0009438 cricoid and tracheal cartilage fusion IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0009569 abnormal left lung morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0009570 abnormal right lung morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0009571 abnormal right lung accessory lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0010565 absent fetal ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0010572 persistent right dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0010584 abnormal conotruncus septation IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010595 abnormal aortic valve cusp morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0010701 fusion of atlas and odontoid process IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010702 split cervical atlas IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010703 split cervical axis IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010705 absent metoptic pillar IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010706 ventral rotation of lens IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010706 ventral rotation of lens IAGP N RGD:5509061 20160324 MGI PMID:16207763 11217 Rarb retinoic acid receptor, beta gene MP:0010707 decreased ventral retina size IAGP N RGD:5509061 20160324 MGI PMID:16207763 11217 Rarb retinoic acid receptor, beta gene MP:0010709 absent eye anterior chamber IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0010709 absent eye anterior chamber IAGP N RGD:5509061 20201119 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010710 absent sclera IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:11857787 11217 Rarb retinoic acid receptor, beta gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:16207763 11217 Rarb retinoic acid receptor, beta gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0010712 absent nasolacrimal duct IAGP N RGD:5509061 20141211 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010712 absent nasolacrimal duct IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0010714 iris coloboma IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010715 retina coloboma IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0010716 optic disk coloboma IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010717 optic nerve coloboma IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0010721 short sublingual duct IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010721 short sublingual duct IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0010722 persistent cervical thymus IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0010722 persistent cervical thymus IAGP N RGD:5509061 20171207 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20141003 MGI PMID:15635054 11217 Rarb retinoic acid receptor, beta gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20141003 MGI PMID:11074013 11217 Rarb retinoic acid receptor, beta gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20141003 MGI PMID:15635054 11217 Rarb retinoic acid receptor, beta gene MP:0010980 ectopic ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:10021334 11217 Rarb retinoic acid receptor, beta gene MP:0010987 abnormal nephrogenic mesenchyme morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10021334 11217 Rarb retinoic acid receptor, beta gene MP:0010989 fused bronchial cartilage rings IAGP N RGD:5509061 20150212 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0010995 abnormal lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:11074013 11217 Rarb retinoic acid receptor, beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:10021334 11217 Rarb retinoic acid receptor, beta gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0011407 absent nephrogenic zone IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0011486 ectopic ureter IAGP N RGD:5509061 20141003 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0011486 ectopic ureter IAGP N RGD:5509061 20141003 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0013331 abnormal lacrimal gland development IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0013439 abnormal Harderian gland development IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0013574 ectopic parathyroid gland IAGP N RGD:5509061 20150305 MGI PMID:7607068 11217 Rarb retinoic acid receptor, beta gene MP:0013744 abnormal conjunctival sac morphology IAGP N RGD:5509061 20150416 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0013744 abnormal conjunctival sac morphology IAGP N RGD:5509061 20160324 MGI PMID:16207763 11217 Rarb retinoic acid receptor, beta gene MP:0013744 abnormal conjunctival sac morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0013826 absent hypoglossal canal IAGP N RGD:5509061 20171026 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:9240560 11217 Rarb retinoic acid receptor, beta gene MP:0030326 decreased periocular mesenchyme apoptosis IAGP N RGD:5509061 20171109 MGI PMID:16207763 11217 Rarb retinoic acid receptor, beta gene MP:0030394 abnormal incus short process morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11217 Rarb retinoic acid receptor, beta gene MP:0030406 absent stapes obturator foramen IAGP N RGD:5509061 20171207 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0000044 absent organ of Corti IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000075 absent neurocranium IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10559481 11218 Rarg retinoic acid receptor, gamma gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000099 absent vomer bone IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000111 cleft palate IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0000154 rib fusion IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000161 scoliosis IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0000435 shortened head IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000445 short snout IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0000553 absent radius IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000562 polydactyly IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000565 oligodactyly IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000914 exencephaly IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000929 open neural tube IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0000935 abnormal folding of telencephalic vesicles IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0001070 abnormal abducens nerve morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:16751185 11218 Rarg retinoic acid receptor, gamma gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 11218 Rarg retinoic acid receptor, gamma gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 11218 Rarg retinoic acid receptor, gamma gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7631783 11218 Rarg retinoic acid receptor, gamma gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10559481 11218 Rarg retinoic acid receptor, gamma gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:16207763 11218 Rarg retinoic acid receptor, gamma gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0001310 abnormal conjunctiva morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:7631783 11218 Rarg retinoic acid receptor, gamma gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10559481 11218 Rarg retinoic acid receptor, gamma gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11857788 11218 Rarg retinoic acid receptor, gamma gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 11218 Rarg retinoic acid receptor, gamma gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7631783 11218 Rarg retinoic acid receptor, gamma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0002257 abnormal arytenoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 11218 Rarg retinoic acid receptor, gamma gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0002765 short fibula IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:16751185 11218 Rarg retinoic acid receptor, gamma gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10559481 11218 Rarg retinoic acid receptor, gamma gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0003078 aphakia IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0003146 absent cochlear ganglion IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0003558 absent uterus IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0003639 abnormal response to vitamins IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0004358 bowed tibia IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0004380 short frontal bone IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0004550 short trachea IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0004552 fused tracheal cartilage rings IAGP N RGD:5509061 20141003 MGI PMID:7631783 11218 Rarg retinoic acid receptor, gamma gene MP:0004552 fused tracheal cartilage rings IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0004552 fused tracheal cartilage rings IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0004553 absent tracheal cartilage rings IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:14660544 11218 Rarg retinoic acid receptor, gamma gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20141003 MGI PMID:14660544 11218 Rarg retinoic acid receptor, gamma gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:14660544 11218 Rarg retinoic acid receptor, gamma gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:14660544 11218 Rarg retinoic acid receptor, gamma gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0004658 abnormal ventral tubercle of atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:14660544 11218 Rarg retinoic acid receptor, gamma gene MP:0004666 absent stapedial artery IAGP N RGD:5509061 20170921 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0004790 absent upper incisors IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0005208 abnormal iris stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0005248 abnormal Harderian gland morphology IAGP N RGD:5509061 20141003 MGI PMID:7631783 11218 Rarg retinoic acid receptor, gamma gene MP:0005248 abnormal Harderian gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0005579 absent outer ear IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0005623 abnormal meninges morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0006289 otic capsule hypoplasia IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0008514 absent retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0008823 abnormal interventricular septum membranous part morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:7631783 11218 Rarg retinoic acid receptor, gamma gene MP:0008881 absent Harderian gland IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0008881 absent Harderian gland IAGP N RGD:5509061 20150205 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0008881 absent Harderian gland IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0008972 ethmoturbinate hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0009072 absent cranial vagina IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0009075 rudimentary Wolffian ducts IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0009076 rudimentary Mullerian ducts IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0009438 cricoid and tracheal cartilage fusion IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0009438 cricoid and tracheal cartilage fusion IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0009525 abnormal submandibular duct morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0009526 absent sublingual gland IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0009527 abnormal sublingual duct morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 11218 Rarg retinoic acid receptor, gamma gene MP:0010146 umbilical hernia IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0010502 ventricle myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0010565 absent fetal ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0010572 persistent right dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0010701 fusion of atlas and odontoid process IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0010702 split cervical atlas IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0010703 split cervical axis IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0010705 absent metoptic pillar IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0010706 ventral rotation of lens IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0010706 ventral rotation of lens IAGP N RGD:5509061 20160324 MGI PMID:16207763 11218 Rarg retinoic acid receptor, gamma gene MP:0010707 decreased ventral retina size IAGP N RGD:5509061 20160324 MGI PMID:16207763 11218 Rarg retinoic acid receptor, gamma gene MP:0010709 absent eye anterior chamber IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0010709 absent eye anterior chamber IAGP N RGD:5509061 20201119 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0010710 absent sclera IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:16207763 11218 Rarg retinoic acid receptor, gamma gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0010712 absent nasolacrimal duct IAGP N RGD:5509061 20141211 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0010712 absent nasolacrimal duct IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0010713 corneal-lenticular stalk IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0010714 iris coloboma IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0010715 retina coloboma IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0010716 optic disk coloboma IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0010717 optic nerve coloboma IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0010720 absent sublingual duct IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0010721 short sublingual duct IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0010721 short sublingual duct IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0010722 persistent cervical thymus IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20141003 MGI PMID:10559481 11218 Rarg retinoic acid receptor, gamma gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20141003 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0010772 abnormal pollex morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0010989 fused bronchial cartilage rings IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0011306 absent kidney pelvis IAGP N RGD:5509061 20141003 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0011486 ectopic ureter IAGP N RGD:5509061 20141003 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0012141 absent hindbrain IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0012247 absent cornea IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0012523 abnormal upper lip morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0013233 ectopic thyroid gland IAGP N RGD:5509061 20150122 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0013319 seminal vesicle atrophy IAGP N RGD:5509061 20141204 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0013321 squamous metaplasia of seminal vesicles IAGP N RGD:5509061 20141204 MGI PMID:11857788 11218 Rarg retinoic acid receptor, gamma gene MP:0013321 squamous metaplasia of seminal vesicles IAGP N RGD:5509061 20141204 MGI PMID:7631783 11218 Rarg retinoic acid receptor, gamma gene MP:0013321 squamous metaplasia of seminal vesicles IAGP N RGD:5509061 20141204 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0013322 squamous metaplasia of prostate gland IAGP N RGD:5509061 20141204 MGI PMID:11857788 11218 Rarg retinoic acid receptor, gamma gene MP:0013322 squamous metaplasia of prostate gland IAGP N RGD:5509061 20141204 MGI PMID:7631783 11218 Rarg retinoic acid receptor, gamma gene MP:0013322 squamous metaplasia of prostate gland IAGP N RGD:5509061 20141204 MGI PMID:8388780 11218 Rarg retinoic acid receptor, gamma gene MP:0013331 abnormal lacrimal gland development IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0013439 abnormal Harderian gland development IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0013574 ectopic parathyroid gland IAGP N RGD:5509061 20150305 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0013744 abnormal conjunctival sac morphology IAGP N RGD:5509061 20150416 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0013744 abnormal conjunctival sac morphology IAGP N RGD:5509061 20160324 MGI PMID:16207763 11218 Rarg retinoic acid receptor, gamma gene MP:0013744 abnormal conjunctival sac morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:9240560 11218 Rarg retinoic acid receptor, gamma gene MP:0030137 abnormal upper incisor morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0030200 abnormal nasal septum cartilage morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0030304 abnormal cribriform plate morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0030326 decreased periocular mesenchyme apoptosis IAGP N RGD:5509061 20171109 MGI PMID:16207763 11218 Rarg retinoic acid receptor, gamma gene MP:0030394 abnormal incus short process morphology IAGP N RGD:5509061 20200102 MGI PMID:7607067 11218 Rarg retinoic acid receptor, gamma gene MP:0030416 absent temporal bone zygomatic process IAGP N RGD:5509061 20171214 MGI PMID:9376317 11218 Rarg retinoic acid receptor, gamma gene MP:0030867 small thyroid cartilage IAGP N RGD:5509061 20181101 MGI PMID:7607068 11218 Rarg retinoic acid receptor, gamma gene MP:0031445 midline cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:7607067 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:15653467 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:15843406 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:16648263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:8957005 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:1406933 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:7925271 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:8957005 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15743840 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17363591 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12498715 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22556269 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:16227443 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:1406933 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12529408 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:1406933 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:7925271 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7925270 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19506017 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000631 abnormal neuroendocrine gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8134105 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9537419 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:12529408 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:8957005 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10783170 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8957005 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000798 abnormal frontal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000828 abnormal fourth ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000829 dilated fourth ventricle IAGP N RGD:5509061 20141003 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12810584 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:12810584 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12810584 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:12810584 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12810584 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7925270 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:7925270 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12810584 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:12810584 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23858447 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23858447 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:22611036 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16103190 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16103190 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:16103190 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:8134105 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151008 MGI PMID:24292676 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16227443 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:12839925 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17893233 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18559481 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23047698 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23486187 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:8134105 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20151008 MGI PMID:24292676 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20220519 MGI PMID:34099734 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20230608 MGI PMID:33594717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:7925270 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17235288 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17363591 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:17363591 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:8957005 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10783170 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12810584 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10783170 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:16648263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10783170 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20141003 MGI PMID:12360286 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:12529408 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:8957005 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:16648263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:10783170 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:1406933 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18559481 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15743840 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:1406933 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:1406933 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23079656 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001885 mammary gland duct hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19506017 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001885 mammary gland duct hyperplasia IAGP N RGD:5509061 20150212 MGI PMID:24662053 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23858447 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15743840 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20150212 MGI PMID:24662053 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:15653467 11219 Rb1 RB transcriptional corepressor 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:16648263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:7925270 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:22574128 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12096340 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16029419 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18559481 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19176372 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22556269 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:7951317 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9537419 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19151761 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19765830 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:14522252 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7951317 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20151008 MGI PMID:24292676 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7951317 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20676140 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22574128 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002039 increased neuroblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9214616 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7925270 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8134105 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9671308 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16227443 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12498715 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15653467 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23047698 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12234974 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12498715 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15743840 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16227443 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17235288 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17893233 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18559481 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19151761 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20406986 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21788502 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22574128 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22611036 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23486187 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7951317 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9537419 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9671308 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20160512 MGI PMID:17637742 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20161013 MGI PMID:26659571 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20220519 MGI PMID:34099734 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20230601 MGI PMID:30093633 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20230608 MGI PMID:33594717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20230615 MGI PMID:28655788 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12234974 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:23858447 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15743840 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20027616 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9671308 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:12529408 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:7925271 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:19151761 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:12498715 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:1406933 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:1406933 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16648263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002623 abnormal vestibular hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15843406 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002623 abnormal vestibular hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16648263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16227443 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20151008 MGI PMID:24292676 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15743840 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:7925271 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:8957005 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16029419 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:9537419 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16227443 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:23486187 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16271529 11219 Rb1 RB transcriptional corepressor 1 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17235288 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:8957005 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12529408 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12810584 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:1406933 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003315 abnormal perineum morphology IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21573126 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21875955 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:12810584 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003365 increased glucagonoma incidence IAGP N RGD:5509061 20151008 MGI PMID:24292676 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20230608 MGI PMID:33594717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:12096340 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:12234974 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:19151761 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:7951317 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20230601 MGI PMID:35700263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003496 increased thyroid adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9537419 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12839925 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:19506017 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:16612004 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20676140 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20230601 MGI PMID:30093633 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003745 abnormal oral mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:19176372 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:17043311 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18559481 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23486187 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20161013 MGI PMID:26659571 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:29743593 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:30093633 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:35700263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:36073547 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230608 MGI PMID:33594717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230615 MGI PMID:28655788 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003838 abnormal milk ejection IAGP N RGD:5509061 20141003 MGI PMID:19506017 11219 Rb1 RB transcriptional corepressor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:16612004 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:15843406 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:21573126 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:16612004 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12810584 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12810584 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12810584 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:8957005 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20676140 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:15743840 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004265 abnormal placental transport IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16648263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004327 increased vestibular hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15653467 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004327 increased vestibular hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15843406 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:15843406 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16648263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15653467 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15843406 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16648263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16648263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15653467 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15843406 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16648263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16648263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004407 increased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15653467 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004407 increased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15843406 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004478 increased testicular teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16227443 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004498 increased organ of Corti supporting cell number IAGP N RGD:5509061 20141003 MGI PMID:15843406 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15843406 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:15743840 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16648263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:15843406 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:8957005 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004840 increased Deiters cell number IAGP N RGD:5509061 20141003 MGI PMID:15653467 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23858447 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004898 uterine hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9537419 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:12810584 11219 Rb1 RB transcriptional corepressor 1 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:15353549 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:12529408 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21788502 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23079656 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23079656 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:1406933 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:7925270 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:8134105 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005161 hematuria IAGP N RGD:5509061 20160915 MGI PMID:25252918 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:12360286 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:17363591 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:12529408 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17235288 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005299 abnormal eye posterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:17363591 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15743840 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005488 bronchial epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7951317 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:12529408 11219 Rb1 RB transcriptional corepressor 1 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:8957005 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15843406 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8957005 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12360286 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16227443 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17235288 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17235288 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12360286 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006087 increased body mass index IAGP N RGD:5509061 20141003 MGI PMID:12584165 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006096 absent retina bipolar cells IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006096 absent retina bipolar cells IAGP N RGD:5509061 20141003 MGI PMID:17235288 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:7925270 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10783170 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22574128 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006310 increased retinoblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006310 increased retinoblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17235288 11219 Rb1 RB transcriptional corepressor 1 gene MP:0006310 increased retinoblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17363591 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12839925 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19151761 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19765830 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20406986 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20676140 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21573126 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008068 absent retina ganglion cell IAGP N RGD:5509061 20141003 MGI PMID:17235288 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008130 abnormal pituitary intermediate lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:9671308 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:11076674 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008301 adrenal medulla hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9537419 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008306 abnormal organ of Corti supporting cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15653467 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008306 abnormal organ of Corti supporting cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16648263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008371 pituitary intermediate lobe hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9671308 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:17235288 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008534 enlarged fourth ventricle IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:14522252 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008715 increased lung small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19765830 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008715 increased lung small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20406986 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008715 increased lung small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22611036 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008715 increased lung small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23047698 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008715 increased lung small cell carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:14522252 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008796 increased lens fiber apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:20676140 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:17043311 11219 Rb1 RB transcriptional corepressor 1 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20150212 MGI PMID:24662053 11219 Rb1 RB transcriptional corepressor 1 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 11219 Rb1 RB transcriptional corepressor 1 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20220519 MGI PMID:34099734 11219 Rb1 RB transcriptional corepressor 1 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0009320 increased lymphoblastic lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 11219 Rb1 RB transcriptional corepressor 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12529408 11219 Rb1 RB transcriptional corepressor 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0009408 decreased skeletal muscle fiber density IAGP N RGD:5509061 20141003 MGI PMID:8957005 11219 Rb1 RB transcriptional corepressor 1 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20150212 MGI PMID:24662053 11219 Rb1 RB transcriptional corepressor 1 gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20160915 MGI PMID:25252918 11219 Rb1 RB transcriptional corepressor 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12360286 11219 Rb1 RB transcriptional corepressor 1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12360286 11219 Rb1 RB transcriptional corepressor 1 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20230615 MGI PMID:28655788 11219 Rb1 RB transcriptional corepressor 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:12529408 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:12670909 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010281 increased nervous system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23887970 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20676140 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20230601 MGI PMID:30093633 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20230601 MGI PMID:36073547 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12498715 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21788502 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22556269 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23047698 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:7951317 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12498715 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:1406933 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21788502 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22556269 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22574128 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9537419 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20150212 MGI PMID:24662053 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20160512 MGI PMID:17637742 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010321 increased parathyroid gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010344 increased hibernoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23486187 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010345 increased thyroid C-cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010345 increased thyroid C-cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19765830 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:14522252 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010348 increased pancreatic islet cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7951317 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010348 increased pancreatic islet cell carcinoma incidence IAGP N RGD:5509061 20151008 MGI PMID:24292676 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010350 increased pituitary adenohypophysis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12096340 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010350 increased pituitary adenohypophysis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010350 increased pituitary adenohypophysis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010351 increased pituitary melanotroph tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12096340 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010351 increased pituitary melanotroph tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010351 increased pituitary melanotroph tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010351 increased pituitary melanotroph tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:7925271 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010351 increased pituitary melanotroph tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:7951317 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20220519 MGI PMID:34099734 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20160204 MGI PMID:14522252 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20230608 MGI PMID:33594717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0010918 abnormal pulmonary neuroendocrine body morphology IAGP N RGD:5509061 20141003 MGI PMID:23047698 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16029419 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20150212 MGI PMID:24662053 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12529408 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20150212 MGI PMID:24662053 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8957005 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9537419 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21788502 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12096340 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12498715 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1406932 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1406933 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12360286 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16029419 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:21788502 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:16449662 11219 Rb1 RB transcriptional corepressor 1 gene MP:0011804 increased cell migration IAGP N RGD:5509061 20161013 MGI PMID:26659571 11219 Rb1 RB transcriptional corepressor 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16227443 11219 Rb1 RB transcriptional corepressor 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20200409 MGI PMID:27889452 11219 Rb1 RB transcriptional corepressor 1 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:29743593 11219 Rb1 RB transcriptional corepressor 1 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:33594717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:35700263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230615 MGI PMID:28655788 11219 Rb1 RB transcriptional corepressor 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:12839925 11219 Rb1 RB transcriptional corepressor 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:16029419 11219 Rb1 RB transcriptional corepressor 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:21573126 11219 Rb1 RB transcriptional corepressor 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:24292676 11219 Rb1 RB transcriptional corepressor 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:27889452 11219 Rb1 RB transcriptional corepressor 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:29743593 11219 Rb1 RB transcriptional corepressor 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:35700263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:8682293 11219 Rb1 RB transcriptional corepressor 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:9671308 11219 Rb1 RB transcriptional corepressor 1 gene MP:0021056 abnormal tumor vascular morphology IAGP N RGD:5509061 20230601 MGI PMID:35700263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:15231717 11219 Rb1 RB transcriptional corepressor 1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:17235288 11219 Rb1 RB transcriptional corepressor 1 gene MP:0030006 decreased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:12360286 11219 Rb1 RB transcriptional corepressor 1 gene MP:0030047 flat forehead IAGP N RGD:5509061 20170921 MGI PMID:1406937 11219 Rb1 RB transcriptional corepressor 1 gene MP:0031278 decreased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:29743593 11219 Rb1 RB transcriptional corepressor 1 gene MP:0031278 decreased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:35700263 11219 Rb1 RB transcriptional corepressor 1 gene MP:0031278 decreased osteosarcoma incidence IAGP N RGD:5509061 20230615 MGI PMID:28655788 11219 Rb1 RB transcriptional corepressor 1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15743840 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15743840 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000397 abnormal guard hair morphology IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:19151761 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17235288 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15743840 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15743840 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19151761 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15743840 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17235288 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19151761 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20406986 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:19151761 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002683 delayed fertility IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15743840 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002765 short fibula IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17235288 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0003109 short femur IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21875955 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:19151761 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:19151761 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:15231717 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:15743840 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004347 abnormal scapular spine morphology IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004355 short radius IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004385 interparietal bone hypoplasia IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004385 interparietal bone hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004444 small supraoccipital bone IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:15743840 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0005161 hematuria IAGP N RGD:5509061 20160915 MGI PMID:25252918 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17235288 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15743840 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17235288 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17235288 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15231717 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0006096 absent retina bipolar cells IAGP N RGD:5509061 20141003 MGI PMID:17235288 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0006310 increased retinoblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15231717 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0006310 increased retinoblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17235288 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19151761 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20406986 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0008068 absent retina ganglion cell IAGP N RGD:5509061 20141003 MGI PMID:17235288 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0008160 increased diameter of humerus IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0008161 increased diameter of radius IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0008163 increased diameter of ulna IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0008218 delayed emergence of vibrissae IAGP N RGD:5509061 20141003 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:17235288 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0008715 increased lung small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20406986 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20160915 MGI PMID:25252918 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20150212 MGI PMID:24710275 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0013168 absent hindlimb buds IAGP N RGD:5509061 20150528 MGI PMID:9806916 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:15231717 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:8682294 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:17235288 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0030079 small incisors IAGP N RGD:5509061 20170928 MGI PMID:12702649 11220 Rbl2 RB transcriptional corepressor like 2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15743840 11221 Rbp1 retinol binding protein 1, cellular gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11222375 11221 Rbp1 retinol binding protein 1, cellular gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:11222375 11221 Rbp1 retinol binding protein 1, cellular gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:10487743 11221 Rbp1 retinol binding protein 1, cellular gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:10487743 11221 Rbp1 retinol binding protein 1, cellular gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:10487743 11221 Rbp1 retinol binding protein 1, cellular gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:10487743 11221 Rbp1 retinol binding protein 1, cellular gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10487743 11221 Rbp1 retinol binding protein 1, cellular gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10487743 11221 Rbp1 retinol binding protein 1, cellular gene MP:0003011 delayed dark adaptation IAGP N RGD:5509061 20141003 MGI PMID:12036972 11221 Rbp1 retinol binding protein 1, cellular gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:10487743 11221 Rbp1 retinol binding protein 1, cellular gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10487743 11221 Rbp1 retinol binding protein 1, cellular gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:10487743 11221 Rbp1 retinol binding protein 1, cellular gene MP:0005444 abnormal retinol metabolism IAGP N RGD:5509061 20141003 MGI PMID:10487743 11221 Rbp1 retinol binding protein 1, cellular gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10487743 11221 Rbp1 retinol binding protein 1, cellular gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 11221 Rbp1 retinol binding protein 1, cellular gene MP:0011234 abnormal retinol level IAGP N RGD:5509061 20141003 MGI PMID:10487743 11221 Rbp1 retinol binding protein 1, cellular gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10487743 11221 Rbp1 retinol binding protein 1, cellular gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 11226 Rbp2 retinol binding protein 2, cellular gene MP:0001671 abnormal vitamin absorption IAGP N RGD:5509061 20141003 MGI PMID:12138113 11226 Rbp2 retinol binding protein 2, cellular gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:12138113 11226 Rbp2 retinol binding protein 2, cellular gene MP:0011234 abnormal retinol level IAGP N RGD:5509061 20141003 MGI PMID:12138113 11227 Rbp3 retinol binding protein 3, interstitial gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:9614228 11227 Rbp3 retinol binding protein 3, interstitial gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:9614228 11227 Rbp3 retinol binding protein 3, interstitial gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:10508404 11227 Rbp3 retinol binding protein 3, interstitial gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:9614228 11227 Rbp3 retinol binding protein 3, interstitial gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:9614228 11227 Rbp3 retinol binding protein 3, interstitial gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:9614228 11234 Ret ret proto-oncogene gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11641220 11234 Ret ret proto-oncogene gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:16565500 11234 Ret ret proto-oncogene gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:18414682 11234 Ret ret proto-oncogene gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:15340065 11234 Ret ret proto-oncogene gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:15469971 11234 Ret ret proto-oncogene gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:17050626 11234 Ret ret proto-oncogene gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:15340065 11234 Ret ret proto-oncogene gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:16565500 11234 Ret ret proto-oncogene gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:10675330 11234 Ret ret proto-oncogene gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:11641220 11234 Ret ret proto-oncogene gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:16565500 11234 Ret ret proto-oncogene gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:17047028 11234 Ret ret proto-oncogene gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:17065462 11234 Ret ret proto-oncogene gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:17372903 11234 Ret ret proto-oncogene gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:18414682 11234 Ret ret proto-oncogene gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:20392943 11234 Ret ret proto-oncogene gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:7595168 11234 Ret ret proto-oncogene gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:8114940 11234 Ret ret proto-oncogene gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:15469971 11234 Ret ret proto-oncogene gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:18216204 11234 Ret ret proto-oncogene gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:7595168 11234 Ret ret proto-oncogene gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:8114940 11234 Ret ret proto-oncogene gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:16565500 11234 Ret ret proto-oncogene gene MP:0000576 clubfoot IAGP N RGD:5509061 20141003 MGI PMID:16600854 11234 Ret ret proto-oncogene gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10675330 11234 Ret ret proto-oncogene gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17372903 11234 Ret ret proto-oncogene gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:17553423 11234 Ret ret proto-oncogene gene MP:0000909 abnormal facial motor nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18216204 11234 Ret ret proto-oncogene gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:18305247 11234 Ret ret proto-oncogene gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:18305247 11234 Ret ret proto-oncogene gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:17553423 11234 Ret ret proto-oncogene gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10675330 11234 Ret ret proto-oncogene gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11641220 11234 Ret ret proto-oncogene gene MP:0001014 absent superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:8565847 11234 Ret ret proto-oncogene gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:11641220 11234 Ret ret proto-oncogene gene MP:0001017 abnormal stellate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8565847 11234 Ret ret proto-oncogene gene MP:0001025 abnormal sympathetic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11641220 11234 Ret ret proto-oncogene gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:15340065 11234 Ret ret proto-oncogene gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:15469971 11234 Ret ret proto-oncogene gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:18414682 11234 Ret ret proto-oncogene gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:11562352 11234 Ret ret proto-oncogene gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:15340065 11234 Ret ret proto-oncogene gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:15469971 11234 Ret ret proto-oncogene gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:16227613 11234 Ret ret proto-oncogene gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:16565500 11234 Ret ret proto-oncogene gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:17050626 11234 Ret ret proto-oncogene gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:17372903 11234 Ret ret proto-oncogene gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:18414682 11234 Ret ret proto-oncogene gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12668632 11234 Ret ret proto-oncogene gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16565500 11234 Ret ret proto-oncogene gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17050626 11234 Ret ret proto-oncogene gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17065462 11234 Ret ret proto-oncogene gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20392943 11234 Ret ret proto-oncogene gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:11641220 11234 Ret ret proto-oncogene gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:16565500 11234 Ret ret proto-oncogene gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:17050626 11234 Ret ret proto-oncogene gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:17065462 11234 Ret ret proto-oncogene gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:17553423 11234 Ret ret proto-oncogene gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:20392943 11234 Ret ret proto-oncogene gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:7595168 11234 Ret ret proto-oncogene gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:8114940 11234 Ret ret proto-oncogene gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:8565847 11234 Ret ret proto-oncogene gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:16600854 11234 Ret ret proto-oncogene gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:18216204 11234 Ret ret proto-oncogene gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:15469971 11234 Ret ret proto-oncogene gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15469971 11234 Ret ret proto-oncogene gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15469971 11234 Ret ret proto-oncogene gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:7595168 11234 Ret ret proto-oncogene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20392943 11234 Ret ret proto-oncogene gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:15340065 11234 Ret ret proto-oncogene gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:17553423 11234 Ret ret proto-oncogene gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17065462 11234 Ret ret proto-oncogene gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20180517 MGI PMID:29192291 11234 Ret ret proto-oncogene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11562352 11234 Ret ret proto-oncogene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15340065 11234 Ret ret proto-oncogene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20392943 11234 Ret ret proto-oncogene gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10675330 11234 Ret ret proto-oncogene gene MP:0002039 increased neuroblastoma incidence IAGP N RGD:5509061 20180920 MGI PMID:29321660 11234 Ret ret proto-oncogene gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10675330 11234 Ret ret proto-oncogene gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19321127 11234 Ret ret proto-oncogene gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16227613 11234 Ret ret proto-oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15469971 11234 Ret ret proto-oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20392943 11234 Ret ret proto-oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20180920 MGI PMID:29321660 11234 Ret ret proto-oncogene gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11562352 11234 Ret ret proto-oncogene gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16227613 11234 Ret ret proto-oncogene gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:7595168 11234 Ret ret proto-oncogene gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:8114940 11234 Ret ret proto-oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11562352 11234 Ret ret proto-oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15469971 11234 Ret ret proto-oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15541311 11234 Ret ret proto-oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16227613 11234 Ret ret proto-oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18216204 11234 Ret ret proto-oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20064391 11234 Ret ret proto-oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 11234 Ret ret proto-oncogene gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:15242795 11234 Ret ret proto-oncogene gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:18305247 11234 Ret ret proto-oncogene gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:7595168 11234 Ret ret proto-oncogene gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17553423 11234 Ret ret proto-oncogene gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19755105 11234 Ret ret proto-oncogene gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20141003 MGI PMID:17553423 11234 Ret ret proto-oncogene gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20141003 MGI PMID:18414682 11234 Ret ret proto-oncogene gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:16600854 11234 Ret ret proto-oncogene gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:12783789 11234 Ret ret proto-oncogene gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:16227613 11234 Ret ret proto-oncogene gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:7595168 11234 Ret ret proto-oncogene gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20141003 MGI PMID:18305247 11234 Ret ret proto-oncogene gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11641220 11234 Ret ret proto-oncogene gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18414682 11234 Ret ret proto-oncogene gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20392943 11234 Ret ret proto-oncogene gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:22841315 11234 Ret ret proto-oncogene gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20141003 MGI PMID:10675330 11234 Ret ret proto-oncogene gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20141003 MGI PMID:16227613 11234 Ret ret proto-oncogene gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:12668632 11234 Ret ret proto-oncogene gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:7595168 11234 Ret ret proto-oncogene gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:8114940 11234 Ret ret proto-oncogene gene MP:0003358 abnormal hypaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:18305247 11234 Ret ret proto-oncogene gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11562352 11234 Ret ret proto-oncogene gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15469971 11234 Ret ret proto-oncogene gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16227613 11234 Ret ret proto-oncogene gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17047028 11234 Ret ret proto-oncogene gene MP:0003496 increased thyroid adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17372903 11234 Ret ret proto-oncogene gene MP:0003498 thyroid gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10675330 11234 Ret ret proto-oncogene gene MP:0003585 large ureter IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0003586 dilated ureter IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0003587 ureter obstruction IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0003588 ureter stenosis IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0003600 ectopic kidney IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:17047028 11234 Ret ret proto-oncogene gene MP:0003613 abnormal kidney medulla development IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0003670 dilated renal glomerular capsule IAGP N RGD:5509061 20141003 MGI PMID:7595168 11234 Ret ret proto-oncogene gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:8114940 11234 Ret ret proto-oncogene gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:11562352 11234 Ret ret proto-oncogene gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:15340065 11234 Ret ret proto-oncogene gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:15469971 11234 Ret ret proto-oncogene gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:16227613 11234 Ret ret proto-oncogene gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0003685 abnormal cardiac ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10974669 11234 Ret ret proto-oncogene gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:17047028 11234 Ret ret proto-oncogene gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:7595168 11234 Ret ret proto-oncogene gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:8114940 11234 Ret ret proto-oncogene gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11641220 11234 Ret ret proto-oncogene gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:20392943 11234 Ret ret proto-oncogene gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:20392943 11234 Ret ret proto-oncogene gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:15340065 11234 Ret ret proto-oncogene gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20141003 MGI PMID:17553423 11234 Ret ret proto-oncogene gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:18305247 11234 Ret ret proto-oncogene gene MP:0004281 abnormal hypoglossal nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18216204 11234 Ret ret proto-oncogene gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:15469971 11234 Ret ret proto-oncogene gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:16227613 11234 Ret ret proto-oncogene gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:17047028 11234 Ret ret proto-oncogene gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:8114940 11234 Ret ret proto-oncogene gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:11562352 11234 Ret ret proto-oncogene gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12783789 11234 Ret ret proto-oncogene gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:16227613 11234 Ret ret proto-oncogene gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17047028 11234 Ret ret proto-oncogene gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141016 MGI PMID:24780737 11234 Ret ret proto-oncogene gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:12668632 11234 Ret ret proto-oncogene gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17050626 11234 Ret ret proto-oncogene gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:15340065 11234 Ret ret proto-oncogene gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0008289 abnormal adrenal medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:10675330 11234 Ret ret proto-oncogene gene MP:0008298 adrenergic chromaffin cell hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10675330 11234 Ret ret proto-oncogene gene MP:0008299 adrenal cortical hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17372903 11234 Ret ret proto-oncogene gene MP:0008312 abnormal sympathetic postganglionic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11641220 11234 Ret ret proto-oncogene gene MP:0008313 abnormal parasympathetic postganglionic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10974669 11234 Ret ret proto-oncogene gene MP:0008314 abnormal pterygopalatine ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15469971 11234 Ret ret proto-oncogene gene MP:0008316 abnormal prevertebral ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11641220 11234 Ret ret proto-oncogene gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:17553423 11234 Ret ret proto-oncogene gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20141003 MGI PMID:8674430 11234 Ret ret proto-oncogene gene MP:0009483 enlarged ileum IAGP N RGD:5509061 20141003 MGI PMID:17553423 11234 Ret ret proto-oncogene gene MP:0009485 distended ileum IAGP N RGD:5509061 20141003 MGI PMID:15469971 11234 Ret ret proto-oncogene gene MP:0009843 decreased neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:18414682 11234 Ret ret proto-oncogene gene MP:0009857 absent kidney cortex IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17372903 11234 Ret ret proto-oncogene gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20141003 MGI PMID:22841315 11234 Ret ret proto-oncogene gene MP:0010362 increased ganglioneuroma incidence IAGP N RGD:5509061 20141003 MGI PMID:10675330 11234 Ret ret proto-oncogene gene MP:0010980 ectopic ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0010981 abnormal branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:8674430 11234 Ret ret proto-oncogene gene MP:0010982 abnormal ureteric bud elongation IAGP N RGD:5509061 20141003 MGI PMID:8674430 11234 Ret ret proto-oncogene gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:8674430 11234 Ret ret proto-oncogene gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:8674430 11234 Ret ret proto-oncogene gene MP:0010985 abnormal kidney mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:8114940 11234 Ret ret proto-oncogene gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15340065 11234 Ret ret proto-oncogene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17553423 11234 Ret ret proto-oncogene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20392943 11234 Ret ret proto-oncogene gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10675330 11234 Ret ret proto-oncogene gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11641220 11234 Ret ret proto-oncogene gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16565500 11234 Ret ret proto-oncogene gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17372903 11234 Ret ret proto-oncogene gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7595168 11234 Ret ret proto-oncogene gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8114940 11234 Ret ret proto-oncogene gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18216204 11234 Ret ret proto-oncogene gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11562352 11234 Ret ret proto-oncogene gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17047028 11234 Ret ret proto-oncogene gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8674430 11234 Ret ret proto-oncogene gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:15469971 11234 Ret ret proto-oncogene gene MP:0011407 absent nephrogenic zone IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0011407 absent nephrogenic zone IAGP N RGD:5509061 20141003 MGI PMID:8114940 11234 Ret ret proto-oncogene gene MP:0011410 ectopic testis IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0011438 absent kidney medulla IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0011727 ectopic ovary IAGP N RGD:5509061 20141003 MGI PMID:16452504 11234 Ret ret proto-oncogene gene MP:0011797 blind ureter IAGP N RGD:5509061 20141003 MGI PMID:7595168 11234 Ret ret proto-oncogene gene MP:0011797 blind ureter IAGP N RGD:5509061 20141003 MGI PMID:8114940 11234 Ret ret proto-oncogene gene MP:0012171 oligohydramnios IAGP N RGD:5509061 20141003 MGI PMID:7595168 11234 Ret ret proto-oncogene gene MP:0013001 abnormal enteric neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17050626 11234 Ret ret proto-oncogene gene MP:0013003 absent enteric neural crest cell IAGP N RGD:5509061 20141003 MGI PMID:11562352 11234 Ret ret proto-oncogene gene MP:0013003 absent enteric neural crest cell IAGP N RGD:5509061 20141003 MGI PMID:16227613 11234 Ret ret proto-oncogene gene MP:0013006 abnormal enteric neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:11562352 11234 Ret ret proto-oncogene gene MP:0013006 abnormal enteric neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:17050626 11234 Ret ret proto-oncogene gene MP:0013006 abnormal enteric neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:18414682 11234 Ret ret proto-oncogene gene MP:0013006 abnormal enteric neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:20392943 11234 Ret ret proto-oncogene gene MP:0013006 abnormal enteric neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:8565847 11234 Ret ret proto-oncogene gene MP:0014484 decreased feces water content IAGP N RGD:5509061 20240704 MGI PMID:20392943 11237 Rgn regucalcin gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16585534 11237 Rgn regucalcin gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:19733551 11237 Rgn regucalcin gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:19482009 11237 Rgn regucalcin gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14975739 11237 Rgn regucalcin gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:19482009 11237 Rgn regucalcin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14975739 11237 Rgn regucalcin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16585534 11237 Rgn regucalcin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16728709 11237 Rgn regucalcin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16585534 11237 Rgn regucalcin gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:16728709 11237 Rgn regucalcin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14975739 11237 Rgn regucalcin gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:16500693 11237 Rgn regucalcin gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:14975739 11237 Rgn regucalcin gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19482009 11237 Rgn regucalcin gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:19733551 11237 Rgn regucalcin gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:16500693 11237 Rgn regucalcin gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:16728709 11237 Rgn regucalcin gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12368201 11237 Rgn regucalcin gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:14975739 11237 Rgn regucalcin gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:16585534 11237 Rgn regucalcin gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:16585534 11237 Rgn regucalcin gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:16585534 11237 Rgn regucalcin gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16585534 11237 Rgn regucalcin gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:16728709 11237 Rgn regucalcin gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14975739 11237 Rgn regucalcin gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16585534 11237 Rgn regucalcin gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:14975739 11237 Rgn regucalcin gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14975739 11237 Rgn regucalcin gene MP:0010252 anterior subcapsular cataract IAGP N RGD:5509061 20141003 MGI PMID:22155581 11237 Rgn regucalcin gene MP:0010911 abnormal pulmonary acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:14989739 11237 Rgn regucalcin gene MP:0010911 abnormal pulmonary acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:16728709 11237 Rgn regucalcin gene MP:0011229 abnormal vitamin C level IAGP N RGD:5509061 20141003 MGI PMID:16585534 11237 Rgn regucalcin gene MP:0011229 abnormal vitamin C level IAGP N RGD:5509061 20141003 MGI PMID:19482009 11237 Rgn regucalcin gene MP:0011229 abnormal vitamin C level IAGP N RGD:5509061 20141003 MGI PMID:19733551 11237 Rgn regucalcin gene MP:0011229 abnormal vitamin C level IAGP N RGD:5509061 20141003 MGI PMID:22155581 11237 Rgn regucalcin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:19733551 11237 Rgn regucalcin gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:14975739 11237 Rgn regucalcin gene MP:0030679 decreased hydroxyproline level IAGP N RGD:5509061 20180920 MGI PMID:19482009 11237 Rgn regucalcin gene MP:0030827 femur fracture IAGP N RGD:5509061 20181101 MGI PMID:16585534 11237 Rgn regucalcin gene MP:0030884 rachitic rosary IAGP N RGD:5509061 20181101 MGI PMID:16585534 11238 Rgs16 regulator of G-protein signaling 16 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:22593615 11238 Rgs16 regulator of G-protein signaling 16 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:21357625 11238 Rgs16 regulator of G-protein signaling 16 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:22593615 11238 Rgs16 regulator of G-protein signaling 16 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:22593615 11238 Rgs16 regulator of G-protein signaling 16 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:22593615 11238 Rgs16 regulator of G-protein signaling 16 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22593615 11238 Rgs16 regulator of G-protein signaling 16 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:22593615 11238 Rgs16 regulator of G-protein signaling 16 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:22593615 11238 Rgs16 regulator of G-protein signaling 16 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:22593615 11238 Rgs16 regulator of G-protein signaling 16 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:21357625 11238 Rgs16 regulator of G-protein signaling 16 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:21610730 11239 Rho rhodopsin gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:16979686 11239 Rho rhodopsin gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:22252712 11239 Rho rhodopsin gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:23221340 11239 Rho rhodopsin gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:9020854 11239 Rho rhodopsin gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15161873 11239 Rho rhodopsin gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19741247 11239 Rho rhodopsin gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:9892703 11239 Rho rhodopsin gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:22110080 11239 Rho rhodopsin gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:22252712 11239 Rho rhodopsin gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23221340 11239 Rho rhodopsin gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23940033 11239 Rho rhodopsin gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20150129 MGI PMID:22183357 11239 Rho rhodopsin gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:15184660 11239 Rho rhodopsin gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:15851469 11239 Rho rhodopsin gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:16979686 11239 Rho rhodopsin gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:19741247 11239 Rho rhodopsin gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:21224384 11239 Rho rhodopsin gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:22110080 11239 Rho rhodopsin gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:23940033 11239 Rho rhodopsin gene MP:0001326 retina degeneration IAGP N RGD:5509061 20150129 MGI PMID:21052544 11239 Rho rhodopsin gene MP:0001326 retina degeneration IAGP N RGD:5509061 20150129 MGI PMID:22183357 11239 Rho rhodopsin gene MP:0001326 retina degeneration IAGP N RGD:5509061 20191212 MGI PMID:22809998 11239 Rho rhodopsin gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:15161873 11239 Rho rhodopsin gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:21224384 11239 Rho rhodopsin gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:23221340 11239 Rho rhodopsin gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:9892703 11239 Rho rhodopsin gene MP:0001999 photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:20207741 11239 Rho rhodopsin gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:9892703 11239 Rho rhodopsin gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19741247 11239 Rho rhodopsin gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:23221340 11239 Rho rhodopsin gene MP:0003011 delayed dark adaptation IAGP N RGD:5509061 20141003 MGI PMID:20207741 11239 Rho rhodopsin gene MP:0003099 retina detachment IAGP N RGD:5509061 20141003 MGI PMID:23221340 11239 Rho rhodopsin gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16979686 11239 Rho rhodopsin gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21224384 11239 Rho rhodopsin gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20150129 MGI PMID:22183357 11239 Rho rhodopsin gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16979686 11239 Rho rhodopsin gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:20207741 11239 Rho rhodopsin gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15939043 11239 Rho rhodopsin gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19741247 11239 Rho rhodopsin gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11466416 11239 Rho rhodopsin gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16723493 11239 Rho rhodopsin gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17194706 11239 Rho rhodopsin gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21224384 11239 Rho rhodopsin gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22110080 11239 Rho rhodopsin gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23221340 11239 Rho rhodopsin gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:9020854 11239 Rho rhodopsin gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20171207 MGI PMID:28859131 11239 Rho rhodopsin gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21224384 11239 Rho rhodopsin gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23221340 11239 Rho rhodopsin gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:9020854 11239 Rho rhodopsin gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:19741247 11239 Rho rhodopsin gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20207741 11239 Rho rhodopsin gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20171207 MGI PMID:28859131 11239 Rho rhodopsin gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11466416 11239 Rho rhodopsin gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15161873 11239 Rho rhodopsin gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16723493 11239 Rho rhodopsin gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19741247 11239 Rho rhodopsin gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15161873 11239 Rho rhodopsin gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15161873 11239 Rho rhodopsin gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15161873 11239 Rho rhodopsin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:11466416 11239 Rho rhodopsin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:15161873 11239 Rho rhodopsin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:15939043 11239 Rho rhodopsin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:16979686 11239 Rho rhodopsin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:20081859 11239 Rho rhodopsin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:20207741 11239 Rho rhodopsin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21224384 11239 Rho rhodopsin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:22110080 11239 Rho rhodopsin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:23221340 11239 Rho rhodopsin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20171214 MGI PMID:28859131 11239 Rho rhodopsin gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21224384 11239 Rho rhodopsin gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20141003 MGI PMID:15851469 11239 Rho rhodopsin gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20141003 MGI PMID:21224384 11239 Rho rhodopsin gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15939043 11239 Rho rhodopsin gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21224384 11239 Rho rhodopsin gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20150129 MGI PMID:22183357 11239 Rho rhodopsin gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:11466416 11239 Rho rhodopsin gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15851469 11239 Rho rhodopsin gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:16979686 11239 Rho rhodopsin gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21224384 11239 Rho rhodopsin gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:22252712 11239 Rho rhodopsin gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:23221340 11239 Rho rhodopsin gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:9020854 11239 Rho rhodopsin gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:9892703 11239 Rho rhodopsin gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20150129 MGI PMID:22183357 11239 Rho rhodopsin gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20207741 11239 Rho rhodopsin gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:19741247 11239 Rho rhodopsin gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:20207741 11239 Rho rhodopsin gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:9892703 11239 Rho rhodopsin gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20191212 MGI PMID:22809998 11239 Rho rhodopsin gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20150129 MGI PMID:22183357 11239 Rho rhodopsin gene MP:0008581 disorganized photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:20207741 11239 Rho rhodopsin gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:19741247 11239 Rho rhodopsin gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:20081859 11239 Rho rhodopsin gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:23940033 11239 Rho rhodopsin gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:9020854 11239 Rho rhodopsin gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:9892703 11239 Rho rhodopsin gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:20207741 11239 Rho rhodopsin gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:21224384 11239 Rho rhodopsin gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:23221340 11239 Rho rhodopsin gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:9020854 11239 Rho rhodopsin gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:19741247 11239 Rho rhodopsin gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:22252712 11239 Rho rhodopsin gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:9020854 11239 Rho rhodopsin gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:9892703 11239 Rho rhodopsin gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20191212 MGI PMID:22809998 11239 Rho rhodopsin gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23221340 11239 Rho rhodopsin gene MP:0011234 abnormal retinol level IAGP N RGD:5509061 20141003 MGI PMID:20207741 11239 Rho rhodopsin gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20171207 MGI PMID:28859131 11239 Rho rhodopsin gene MP:0012034 abnormal a-wave shape IAGP N RGD:5509061 20191212 MGI PMID:22809998 11239 Rho rhodopsin gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20141003 MGI PMID:22252712 11239 Rho rhodopsin gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20141003 MGI PMID:22252712 11239 Rho rhodopsin gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:15851469 11239 Rho rhodopsin gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:21224384 11239 Rho rhodopsin gene MP:0020439 absent b-wave IAGP N RGD:5509061 20191212 MGI PMID:22809998 11239 Rho rhodopsin gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:19741247 11239 Rho rhodopsin gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:20207741 11239 Rho rhodopsin gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:23940033 11239 Rho rhodopsin gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:9020854 11239 Rho rhodopsin gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:9892703 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20151112 MGI PMID:25910808 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23271052 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19456252 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12832488 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19456252 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:19456252 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20151112 MGI PMID:18718479 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20151112 MGI PMID:25910808 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:12832488 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12832488 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12832488 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12832488 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20151112 MGI PMID:25910808 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20151112 MGI PMID:25910808 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20151112 MGI PMID:18718479 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20151112 MGI PMID:18718479 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20160128 MGI PMID:24135024 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0005260 ocular hypotension IAGP N RGD:5509061 20141003 MGI PMID:19456252 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20151112 MGI PMID:25910808 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20141003 MGI PMID:23271052 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20160128 MGI PMID:24135024 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20151112 MGI PMID:25910808 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:19456252 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20151112 MGI PMID:18718479 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19456252 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160128 MGI PMID:24135024 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12832488 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0012046 decreased susceptibility to hypertension IAGP N RGD:5509061 20160128 MGI PMID:24135024 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0020510 increased dendritic spine length IAGP N RGD:5509061 20211014 MGI PMID:18718479 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20190704 MGI PMID:18718479 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0031212 decreased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:19456252 11243 Rock2 Rho-associated coiled-coil containing protein kinase 2 gene MP:0031509 decreased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:24135024 11244 Ros1 Ros1 proto-oncogene gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:8675006 11244 Ros1 Ros1 proto-oncogene gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10906072 11244 Ros1 Ros1 proto-oncogene gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:24971615 11244 Ros1 Ros1 proto-oncogene gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8675006 11244 Ros1 Ros1 proto-oncogene gene MP:0001925 male infertility IAGP N RGD:5509061 20201022 MGI PMID:32499443 11244 Ros1 Ros1 proto-oncogene gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:8675006 11244 Ros1 Ros1 proto-oncogene gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:8675006 11244 Ros1 Ros1 proto-oncogene gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10906072 11244 Ros1 Ros1 proto-oncogene gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220714 MGI PMID:24971615 11244 Ros1 Ros1 proto-oncogene gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24971615 11244 Ros1 Ros1 proto-oncogene gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8675006 11244 Ros1 Ros1 proto-oncogene gene MP:0004935 epididymis degeneration IAGP N RGD:5509061 20230601 MGI PMID:37095084 11244 Ros1 Ros1 proto-oncogene gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:10906072 11244 Ros1 Ros1 proto-oncogene gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:24971615 11244 Ros1 Ros1 proto-oncogene gene MP:0009248 small caput epididymis IAGP N RGD:5509061 20141003 MGI PMID:8675006 11244 Ros1 Ros1 proto-oncogene gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220714 MGI PMID:24971615 11244 Ros1 Ros1 proto-oncogene gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20201022 MGI PMID:32499443 11244 Ros1 Ros1 proto-oncogene gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220303 MGI PMID:10906072 11244 Ros1 Ros1 proto-oncogene gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220303 MGI PMID:8675006 11247 Rrm1 ribonucleotide reductase M1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20160707 MGI PMID:26077802 11247 Rrm1 ribonucleotide reductase M1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 11247 Rrm1 ribonucleotide reductase M1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 11248 Rrm2 ribonucleotide reductase M2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 11248 Rrm2 ribonucleotide reductase M2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11248 Rrm2 ribonucleotide reductase M2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 11249 War warfarin resistance gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20150514 MGI PMID:1063212 11249 War warfarin resistance gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20150514 MGI PMID:1063212 11250 Rxra retinoid X receptor alpha gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16259011 11250 Rxra retinoid X receptor alpha gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:7638202 11250 Rxra retinoid X receptor alpha gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20170824 MGI PMID:10675365 11250 Rxra retinoid X receptor alpha gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0000288 abnormal pericardium morphology IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0000299 failure of atrioventricular cushion closure IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:16259011 11250 Rxra retinoid X receptor alpha gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0000384 distorted hair follicle pattern IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0000389 disorganized outer root sheath cells IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16259011 11250 Rxra retinoid X receptor alpha gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0000597 delayed hepatic development IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12183441 11250 Rxra retinoid X receptor alpha gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:16751185 11250 Rxra retinoid X receptor alpha gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:16751185 11250 Rxra retinoid X receptor alpha gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 11250 Rxra retinoid X receptor alpha gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:16259011 11250 Rxra retinoid X receptor alpha gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:16259011 11250 Rxra retinoid X receptor alpha gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:14742273 11250 Rxra retinoid X receptor alpha gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0001849 ear inflammation IAGP N RGD:5509061 20141003 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 11250 Rxra retinoid X receptor alpha gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:7923367 11250 Rxra retinoid X receptor alpha gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9356169 11250 Rxra retinoid X receptor alpha gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:11493527 11250 Rxra retinoid X receptor alpha gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:7923367 11250 Rxra retinoid X receptor alpha gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11493527 11250 Rxra retinoid X receptor alpha gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:7923367 11250 Rxra retinoid X receptor alpha gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:11493527 11250 Rxra retinoid X receptor alpha gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:11493527 11250 Rxra retinoid X receptor alpha gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11493527 11250 Rxra retinoid X receptor alpha gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:11493527 11250 Rxra retinoid X receptor alpha gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:7923367 11250 Rxra retinoid X receptor alpha gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9550726 11250 Rxra retinoid X receptor alpha gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11250 Rxra retinoid X receptor alpha gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16259011 11250 Rxra retinoid X receptor alpha gene MP:0002434 abnormal T-helper 2 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16259011 11250 Rxra retinoid X receptor alpha gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 11250 Rxra retinoid X receptor alpha gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0003011 delayed dark adaptation IAGP N RGD:5509061 20141003 MGI PMID:14742273 11250 Rxra retinoid X receptor alpha gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:7638202 11250 Rxra retinoid X receptor alpha gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:12183441 11250 Rxra retinoid X receptor alpha gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:14742273 11250 Rxra retinoid X receptor alpha gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14742273 11250 Rxra retinoid X receptor alpha gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0003923 abnormal heart left atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:7638202 11250 Rxra retinoid X receptor alpha gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16751185 11250 Rxra retinoid X receptor alpha gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:14742273 11250 Rxra retinoid X receptor alpha gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:14742273 11250 Rxra retinoid X receptor alpha gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0004058 abnormal ventricle papillary muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0004062 dilated heart right atrium IAGP N RGD:5509061 20231221 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0004126 thin hypodermis IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16259011 11250 Rxra retinoid X receptor alpha gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0004971 dermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:14742273 11250 Rxra retinoid X receptor alpha gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:9376317 11250 Rxra retinoid X receptor alpha gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14742273 11250 Rxra retinoid X receptor alpha gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:7638202 11250 Rxra retinoid X receptor alpha gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20141003 MGI PMID:14742273 11250 Rxra retinoid X receptor alpha gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0006119 mitral valve atresia IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0006122 mitral valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:7638202 11250 Rxra retinoid X receptor alpha gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:9550726 11250 Rxra retinoid X receptor alpha gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20200618 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0008117 abnormal Langerhans cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0008244 abnormal peritoneal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0008259 abnormal optic disk morphology IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0008542 enlarged cervical lymph nodes IAGP N RGD:5509061 20200618 MGI PMID:16199515 11250 Rxra retinoid X receptor alpha gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:14742273 11250 Rxra retinoid X receptor alpha gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:14742273 11250 Rxra retinoid X receptor alpha gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0008860 abnormal hair cycle telogen phase IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0008881 absent Harderian gland IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:12183441 11250 Rxra retinoid X receptor alpha gene MP:0009555 abnormal hair follicle melanin granule distribution IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0009612 thick epidermis suprabasal layer IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0009736 abnormal prostate gland branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12183441 11250 Rxra retinoid X receptor alpha gene MP:0010064 increased circulating creatine level IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:7638202 11250 Rxra retinoid X receptor alpha gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0010455 aortopulmonary window IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0010457 pulmonary artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:7638202 11250 Rxra retinoid X receptor alpha gene MP:0010559 heart block IAGP N RGD:5509061 20141003 MGI PMID:7638202 11250 Rxra retinoid X receptor alpha gene MP:0010584 abnormal conotruncus septation IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0010640 ventricular myocardium compact layer hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0010640 ventricular myocardium compact layer hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0010706 ventral rotation of lens IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0010707 decreased ventral retina size IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0010710 absent sclera IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0010716 optic disk coloboma IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0010720 absent sublingual duct IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11493527 11250 Rxra retinoid X receptor alpha gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9550726 11250 Rxra retinoid X receptor alpha gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20170824 MGI PMID:10675365 11250 Rxra retinoid X receptor alpha gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0011369 increased renal glomerulus apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:21135166 11250 Rxra retinoid X receptor alpha gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0012802 increased rhombomere 5 size IAGP N RGD:5509061 20141003 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0013269 third pharyngeal arch hypoplasia IAGP N RGD:5509061 20171109 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231221 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0021160 decreased heart right ventricle wall thickness IAGP N RGD:5509061 20231221 MGI PMID:8823298 11250 Rxra retinoid X receptor alpha gene MP:0030335 absent third pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:19255444 11250 Rxra retinoid X receptor alpha gene MP:0030570 abnormal piliary canal morphology IAGP N RGD:5509061 20180524 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0030571 dilated piliary canal IAGP N RGD:5509061 20180524 MGI PMID:11171393 11250 Rxra retinoid X receptor alpha gene MP:0031530 abnormal heart ventricle shape IAGP N RGD:5509061 20240104 MGI PMID:7638202 11250 Rxra retinoid X receptor alpha gene MP:0031530 abnormal heart ventricle shape IAGP N RGD:5509061 20240104 MGI PMID:7926783 11250 Rxra retinoid X receptor alpha gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:7638202 11251 Rxrb retinoid X receptor beta gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:8557197 11251 Rxrb retinoid X receptor beta gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:8557197 11251 Rxrb retinoid X receptor beta gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:16751185 11251 Rxrb retinoid X receptor beta gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:16751185 11251 Rxrb retinoid X receptor beta gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 11251 Rxrb retinoid X receptor beta gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:19255444 11251 Rxrb retinoid X receptor beta gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:19255444 11251 Rxrb retinoid X receptor beta gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:19255444 11251 Rxrb retinoid X receptor beta gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:9883728 11251 Rxrb retinoid X receptor beta gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:9883728 11251 Rxrb retinoid X receptor beta gene MP:0001849 ear inflammation IAGP N RGD:5509061 20141003 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:9883728 11251 Rxrb retinoid X receptor beta gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8557197 11251 Rxrb retinoid X receptor beta gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 11251 Rxrb retinoid X receptor beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16751185 11251 Rxrb retinoid X receptor beta gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:8557197 11251 Rxrb retinoid X receptor beta gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:8557197 11251 Rxrb retinoid X receptor beta gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 11251 Rxrb retinoid X receptor beta gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8557197 11251 Rxrb retinoid X receptor beta gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8557197 11251 Rxrb retinoid X receptor beta gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14993927 11251 Rxrb retinoid X receptor beta gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:19255444 11251 Rxrb retinoid X receptor beta gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:9883728 11251 Rxrb retinoid X receptor beta gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20141003 MGI PMID:14993927 11251 Rxrb retinoid X receptor beta gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16751185 11251 Rxrb retinoid X receptor beta gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19255444 11251 Rxrb retinoid X receptor beta gene MP:0004971 dermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:19255444 11251 Rxrb retinoid X receptor beta gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8557197 11251 Rxrb retinoid X receptor beta gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:19255444 11251 Rxrb retinoid X receptor beta gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20200618 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0008542 enlarged cervical lymph nodes IAGP N RGD:5509061 20200618 MGI PMID:16199515 11251 Rxrb retinoid X receptor beta gene MP:0008839 absent acrosome IAGP N RGD:5509061 20141003 MGI PMID:8557197 11251 Rxrb retinoid X receptor beta gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:8557197 11251 Rxrb retinoid X receptor beta gene MP:0009231 detached acrosome IAGP N RGD:5509061 20141003 MGI PMID:8557197 11251 Rxrb retinoid X receptor beta gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:8557197 11251 Rxrb retinoid X receptor beta gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:8557197 11251 Rxrb retinoid X receptor beta gene MP:0010584 abnormal conotruncus septation IAGP N RGD:5509061 20141003 MGI PMID:19255444 11251 Rxrb retinoid X receptor beta gene MP:0010640 ventricular myocardium compact layer hypoplasia IAGP N RGD:5509061 20240118 MGI PMID:19255444 11251 Rxrb retinoid X receptor beta gene MP:0010706 ventral rotation of lens IAGP N RGD:5509061 20141003 MGI PMID:19255444 11251 Rxrb retinoid X receptor beta gene MP:0010716 optic disk coloboma IAGP N RGD:5509061 20141003 MGI PMID:19255444 11251 Rxrb retinoid X receptor beta gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8557197 11251 Rxrb retinoid X receptor beta gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8557197 11251 Rxrb retinoid X receptor beta gene MP:0012802 increased rhombomere 5 size IAGP N RGD:5509061 20141003 MGI PMID:19255444 11251 Rxrb retinoid X receptor beta gene MP:0013269 third pharyngeal arch hypoplasia IAGP N RGD:5509061 20171109 MGI PMID:19255444 11251 Rxrb retinoid X receptor beta gene MP:0030335 absent third pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:19255444 11252 S100b S100 protein, beta polypeptide, neural gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11872254 11252 S100b S100 protein, beta polypeptide, neural gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160915 MGI PMID:24652767 11252 S100b S100 protein, beta polypeptide, neural gene MP:0003177 allodynia IAGP N RGD:5509061 20141003 MGI PMID:16600520 11252 S100b S100 protein, beta polypeptide, neural gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20160804 MGI 11254 Sag S-antigen, retina and pineal gland (arrestin) gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20201022 MGI 11254 Sag S-antigen, retina and pineal gland (arrestin) gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20150108 MGI 11254 Sag S-antigen, retina and pineal gland (arrestin) gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 11254 Sag S-antigen, retina and pineal gland (arrestin) gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17194706 11254 Sag S-antigen, retina and pineal gland (arrestin) gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:9333241 11254 Sag S-antigen, retina and pineal gland (arrestin) gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18701071 11254 Sag S-antigen, retina and pineal gland (arrestin) gene MP:0004222 iris synechia IEA N RGD:5509061 20201231 MGI 11254 Sag S-antigen, retina and pineal gland (arrestin) gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:9333241 11254 Sag S-antigen, retina and pineal gland (arrestin) gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 11254 Sag S-antigen, retina and pineal gland (arrestin) gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 11258 Atxn1 ataxin 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:17322884 11258 Atxn1 ataxin 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:22053053 11258 Atxn1 ataxin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22053053 11258 Atxn1 ataxin 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20190215 MGI PMID:28288114 11258 Atxn1 ataxin 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17322884 11258 Atxn1 ataxin 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9353120 11258 Atxn1 ataxin 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22053053 11258 Atxn1 ataxin 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10749985 11258 Atxn1 ataxin 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17322884 11258 Atxn1 ataxin 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22053053 11258 Atxn1 ataxin 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23719801 11258 Atxn1 ataxin 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9651231 11258 Atxn1 ataxin 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:9651231 11258 Atxn1 ataxin 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:22014525 11258 Atxn1 ataxin 1 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:22053053 11258 Atxn1 ataxin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17322884 11258 Atxn1 ataxin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22053053 11258 Atxn1 ataxin 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:9651231 11258 Atxn1 ataxin 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:22014525 11258 Atxn1 ataxin 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:17322884 11258 Atxn1 ataxin 1 gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:22053053 11258 Atxn1 ataxin 1 gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:9353120 11258 Atxn1 ataxin 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20190215 MGI PMID:28288114 11258 Atxn1 ataxin 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:9651231 11258 Atxn1 ataxin 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:22014525 11258 Atxn1 ataxin 1 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:22014525 11258 Atxn1 ataxin 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:17322884 11258 Atxn1 ataxin 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20190215 MGI PMID:28288114 11258 Atxn1 ataxin 1 gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20141003 MGI PMID:22014525 11258 Atxn1 ataxin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22014525 11258 Atxn1 ataxin 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22014525 11258 Atxn1 ataxin 1 gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20190215 MGI PMID:28288114 11258 Atxn1 ataxin 1 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:12086639 11258 Atxn1 ataxin 1 gene MP:0020594 decreased cerebral cortex cell number IAGP N RGD:5509061 20190215 MGI PMID:28288114 11258 Atxn1 ataxin 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:28288114 11259 Scg2 secretogranin II gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20220120 MGI PMID:33299180 11264658 Traj33 T cell receptor alpha joining 33 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20191003 MGI PMID:31113973 11266 Scn2b sodium channel, voltage-gated, type II, beta gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12481039 11266 Scn2b sodium channel, voltage-gated, type II, beta gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:12481039 11266 Scn2b sodium channel, voltage-gated, type II, beta gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20170323 MGI 11266 Scn2b sodium channel, voltage-gated, type II, beta gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20220519 MGI 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:18317596 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:21881211 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:18317596 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18317596 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:18317596 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0001954 respiratory distress IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:18317596 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0002690 akinesia IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18317596 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18317596 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:18317596 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:18317596 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0004037 increased muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:18317596 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21881211 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21881211 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18317596 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20211021 MGI 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0009046 muscle twitch IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:18317596 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:18317596 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20150219 MGI PMID:25348630 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18317596 11268 Scn4a sodium channel, voltage-gated, type IV, alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:8589728 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:8589728 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8589728 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9326675 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:8589728 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11857811 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:9326675 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:9326675 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:9326675 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0010109 abnormal renal sodium reabsorption IAGP N RGD:5509061 20141003 MGI PMID:9326675 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9326675 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8589728 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11857811 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0011417 abnormal renal transport IAGP N RGD:5509061 20141003 MGI PMID:20389022 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0011463 decreased urine bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:9326675 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20170921 MGI PMID:9326675 11269 Scnn1a sodium channel, nonvoltage-gated 1 alpha gene MP:0014206 decreased intestinal epithelial sodium ion transmembrane transport IAGP N RGD:5509061 20160526 MGI PMID:9326675 11269910 Iglc1 immunoglobulin lambda constant 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20160630 MGI PMID:11257137 11269910 Iglc1 immunoglobulin lambda constant 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20160630 MGI PMID:11869685 11269910 Iglc1 immunoglobulin lambda constant 1 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20160630 MGI PMID:11257137 11269910 Iglc1 immunoglobulin lambda constant 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20160630 MGI PMID:11257137 11269910 Iglc1 immunoglobulin lambda constant 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20160630 MGI PMID:11257137 11269910 Iglc1 immunoglobulin lambda constant 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160630 MGI PMID:11257137 11269910 Iglc1 immunoglobulin lambda constant 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160630 MGI PMID:11869685 11269910 Iglc1 immunoglobulin lambda constant 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160630 MGI PMID:16860389 11269910 Iglc1 immunoglobulin lambda constant 1 gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20160630 MGI PMID:16860389 11269910 Iglc1 immunoglobulin lambda constant 1 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20160630 MGI PMID:11869685 11269910 Iglc1 immunoglobulin lambda constant 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20160630 MGI PMID:11869685 11269910 Iglc1 immunoglobulin lambda constant 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20160630 MGI PMID:11869685 11269910 Iglc1 immunoglobulin lambda constant 1 gene MP:0008761 abnormal immunoglobulin light chain V-J recombination IAGP N RGD:5509061 20160630 MGI PMID:11869685 11269910 Iglc1 immunoglobulin lambda constant 1 gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20160630 MGI PMID:11869685 11269910 Iglc1 immunoglobulin lambda constant 1 gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20160630 MGI PMID:11869685 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9990092 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10589691 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:10589691 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:10589691 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19036848 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9990093 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:9990092 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:10589691 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:9990092 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0003028 alkalosis IAGP N RGD:5509061 20141003 MGI PMID:10589691 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0004119 hypokalemia IAGP N RGD:5509061 20141003 MGI PMID:10589691 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20141003 MGI PMID:10589691 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20160421 MGI 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:9990092 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0005634 decreased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:9990092 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10589691 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9990092 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0010127 hypervolemia IAGP N RGD:5509061 20141003 MGI PMID:10589691 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19036848 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9990092 11272 Scnn1b sodium channel, nonvoltage-gated 1 beta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11273 Scp2 sterol carrier protein 2, liver gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11673458 11273 Scp2 sterol carrier protein 2, liver gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11673458 11273 Scp2 sterol carrier protein 2, liver gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17068117 11273 Scp2 sterol carrier protein 2, liver gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:17068117 11273 Scp2 sterol carrier protein 2, liver gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:17068117 11273 Scp2 sterol carrier protein 2, liver gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17609524 11273 Scp2 sterol carrier protein 2, liver gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:17068117 11273 Scp2 sterol carrier protein 2, liver gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:9553048 11273 Scp2 sterol carrier protein 2, liver gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9553048 11273 Scp2 sterol carrier protein 2, liver gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11673458 11273 Scp2 sterol carrier protein 2, liver gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:17068117 11273 Scp2 sterol carrier protein 2, liver gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17068117 11273 Scp2 sterol carrier protein 2, liver gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:9553048 11273 Scp2 sterol carrier protein 2, liver gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17068117 11273 Scp2 sterol carrier protein 2, liver gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20141003 MGI PMID:11673458 11273 Scp2 sterol carrier protein 2, liver gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:11673458 11273 Scp2 sterol carrier protein 2, liver gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11673458 11273 Scp2 sterol carrier protein 2, liver gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17068117 11273 Scp2 sterol carrier protein 2, liver gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17068117 11273 Scp2 sterol carrier protein 2, liver gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:9553048 11273 Scp2 sterol carrier protein 2, liver gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:9553048 11273 Scp2 sterol carrier protein 2, liver gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17068117 11273 Scp2 sterol carrier protein 2, liver gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9553048 11273 Scp2 sterol carrier protein 2, liver gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17068117 11273 Scp2 sterol carrier protein 2, liver gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11673458 11273 Scp2 sterol carrier protein 2, liver gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9553048 11273 Scp2 sterol carrier protein 2, liver gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:17068117 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0000122 premature tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:12151080 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23637822 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17135576 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11257138 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:15774854 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17135576 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:18326085 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:20093502 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17473219 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17652758 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23637822 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:19641038 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:20093502 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:16105698 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9734366 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:19641038 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17652758 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20220922 MGI PMID:35775484 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0001987 alcohol preference IAGP N RGD:5509061 20141003 MGI PMID:16105698 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17473219 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17473219 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:17135576 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23603910 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21458307 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16728728 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:19641038 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:23637822 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:19641140 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:14566334 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002570 alcohol aversion IAGP N RGD:5509061 20141003 MGI PMID:16105698 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002620 abnormal monocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17364026 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002620 abnormal monocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9463410 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16691291 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16691291 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:16105698 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16691291 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:11485904 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11257138 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:21458307 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:18326085 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:16691291 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003397 increased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:17135576 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:16105698 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:16105698 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17301181 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:15718500 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:23637822 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:11257138 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15774854 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17135576 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17431224 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:19641140 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:9463410 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:17135576 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:14566334 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:17431224 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18326085 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:9884336 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15774854 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:10395330 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:11257138 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20220922 MGI PMID:35775484 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0004892 increased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:16691291 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:17473219 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:12151080 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17431224 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:19641038 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005098 abnormal optic choroid morphology IAGP N RGD:5509061 20141003 MGI PMID:14566334 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17652758 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:23637822 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9734366 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:17135576 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:9884336 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14566334 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17652758 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:14566334 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17652758 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:23637822 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23637822 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16691291 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17473219 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17473219 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9734366 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:20093502 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20220922 MGI PMID:35775484 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18326085 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:20093502 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17473219 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005546 choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:14566334 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005546 choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:17652758 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23637822 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20141003 MGI PMID:17652758 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20141003 MGI PMID:23637822 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005549 retina pigment epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17652758 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17473219 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:19641038 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11485904 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:9463410 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17473219 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17473219 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0006187 retina deposits IAGP N RGD:5509061 20141003 MGI PMID:14566334 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0006187 retina deposits IAGP N RGD:5509061 20141003 MGI PMID:17652758 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0006238 abnormal choriocapillaris morphology IAGP N RGD:5509061 20141003 MGI PMID:14566334 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16691291 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11257138 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23603910 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17301181 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008243 abnormal macrophage derived foam cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18326085 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:14566334 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:17652758 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:23637822 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11257138 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:14566334 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:16728728 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19641038 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11257138 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16728728 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9463410 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:19641038 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:17652758 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:23637822 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:19641038 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:16728728 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:11257138 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:16728728 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:9463410 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:9463410 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18326085 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:17135576 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:19641140 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:19641140 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:20093502 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20141003 MGI PMID:14566334 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16691201 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17431224 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17473219 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:16691291 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16728728 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0009787 increased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19641038 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0010016 variable depigmentation IAGP N RGD:5509061 20141003 MGI PMID:17652758 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20093502 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0010740 abnormal dendritic cell chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:23603910 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12151080 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:16728728 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:16105698 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:17135576 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:23637822 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:16691291 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:14566334 11275 Ccl2 C-C motif chemokine ligand 2 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:23637822 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15517609 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19729478 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:15155903 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:16105698 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15155903 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11875005 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0002570 alcohol aversion IAGP N RGD:5509061 20141003 MGI PMID:16105698 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:16105698 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20141003 MGI PMID:15155903 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:16105698 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0005614 decreased susceptibility to type III hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:15517609 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:15155903 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:19729478 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15155903 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19729478 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20141003 MGI PMID:11875005 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:16105698 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0020449 decreased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:19729478 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0020938 decreased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:7667639 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0020945 abnormal susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:11875005 11276 Ccl3 C-C motif chemokine ligand 3 gene MP:0020947 decreased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:11875005 11279 Sdc4 syndecan 4 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20201022 MGI 11279 Sdc4 syndecan 4 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:11160142 11279 Sdc4 syndecan 4 gene MP:0002546 mydriasis IEA N RGD:5509061 20170105 MGI 11279 Sdc4 syndecan 4 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:11304570 11279 Sdc4 syndecan 4 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:11160142 11279 Sdc4 syndecan 4 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:10681494 11279 Sdc4 syndecan 4 gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:22869749 11279 Sdc4 syndecan 4 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 11279 Sdc4 syndecan 4 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 11279 Sdc4 syndecan 4 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:11304570 11279 Sdc4 syndecan 4 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 11279 Sdc4 syndecan 4 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11160142 11279 Sdc4 syndecan 4 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11084653 11279 Sdc4 syndecan 4 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11304570 11279 Sdc4 syndecan 4 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18158320 11279 Sdc4 syndecan 4 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 11279 Sdc4 syndecan 4 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:22869749 11279 Sdc4 syndecan 4 gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:22869749 11279 Sdc4 syndecan 4 gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:11304570 11279 Sdc4 syndecan 4 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11304570 11279 Sdc4 syndecan 4 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18158320 11279 Sdc4 syndecan 4 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 11279 Sdc4 syndecan 4 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 11279 Sdc4 syndecan 4 gene MP:0010238 increased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:22869749 11279 Sdc4 syndecan 4 gene MP:0011333 abnormal kidney inner medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:11304570 11279 Sdc4 syndecan 4 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:11160142 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20833981 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23434755 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:9634237 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0000262 poor arterial differentiation IAGP N RGD:5509061 20141003 MGI PMID:23395391 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20850355 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:23434755 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:23434756 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:8757135 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:9689100 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:9689100 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:9689100 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:20833981 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:20850355 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9689100 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:20850355 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20850355 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23434755 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:12707343 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20850355 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:23434755 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:20850355 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:23434756 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20141003 MGI PMID:12684531 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:23035208 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20850355 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20850355 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20833981 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20833981 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20850355 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23434755 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23434756 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20181227 MGI 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23434755 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23434756 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23395391 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20833981 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20850355 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:8757135 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:8757135 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20850355 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23434756 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20850355 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20850355 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:23434756 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20850355 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23434755 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23434756 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:23395391 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:8757135 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20833981 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23434756 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8757135 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23434755 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8757135 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0011816 decreased pre-pro B cell number IAGP N RGD:5509061 20141003 MGI PMID:23434756 11280 Cxcl12 C-X-C motif chemokine ligand 12 gene MP:0014273 abnormal skin vasculature morphology IAGP N RGD:5509061 20230810 MGI PMID:23395391 11283 Sele selectin, endothelial cell gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9329976 11283 Sele selectin, endothelial cell gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10500197 11283 Sele selectin, endothelial cell gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10228023 11283 Sele selectin, endothelial cell gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10500197 11283 Sele selectin, endothelial cell gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11050049 11283 Sele selectin, endothelial cell gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9329976 11283 Sele selectin, endothelial cell gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10500197 11283 Sele selectin, endothelial cell gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:17456770 11283 Sele selectin, endothelial cell gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:17456770 11283 Sele selectin, endothelial cell gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:11050049 11283 Sele selectin, endothelial cell gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9329976 11283 Sele selectin, endothelial cell gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9329976 11283 Sele selectin, endothelial cell gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:10228023 11283 Sele selectin, endothelial cell gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:9329976 11283 Sele selectin, endothelial cell gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9329976 11283 Sele selectin, endothelial cell gene MP:0001411 spinning IAGP N RGD:5509061 20141003 MGI PMID:9329976 11283 Sele selectin, endothelial cell gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20141003 MGI PMID:9329976 11283 Sele selectin, endothelial cell gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:11050049 11283 Sele selectin, endothelial cell gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:10228023 11283 Sele selectin, endothelial cell gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:9329976 11283 Sele selectin, endothelial cell gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7541306 11283 Sele selectin, endothelial cell gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7587631 11283 Sele selectin, endothelial cell gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0002346 abnormal lymph node secondary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0002351 abnormal cervical lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9329976 11283 Sele selectin, endothelial cell gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12096034 11283 Sele selectin, endothelial cell gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:10228023 11283 Sele selectin, endothelial cell gene MP:0002534 abnormal type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:17456770 11283 Sele selectin, endothelial cell gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:11050049 11283 Sele selectin, endothelial cell gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:9789256 11283 Sele selectin, endothelial cell gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10500197 11283 Sele selectin, endothelial cell gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:10228023 11283 Sele selectin, endothelial cell gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:9329976 11283 Sele selectin, endothelial cell gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0008623 increased circulating interleukin-3 level IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:10500197 11283 Sele selectin, endothelial cell gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10228023 11283 Sele selectin, endothelial cell gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:10500197 11283 Sele selectin, endothelial cell gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20240104 MGI PMID:11050049 11283 Sele selectin, endothelial cell gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20240104 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0014351 abnormal spleen B cell follicle shape IAGP N RGD:5509061 20240104 MGI PMID:11050049 11283 Sele selectin, endothelial cell gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:10500197 11283 Sele selectin, endothelial cell gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:11468173 11283 Sele selectin, endothelial cell gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:8598043 11283 Sele selectin, endothelial cell gene MP:0020333 enhanced leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:10500197 11284 Selenow selenoprotein W gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20220120 MGI PMID:33859201 11284 Selenow selenoprotein W gene MP:0001260 increased body weight IAGP N RGD:5509061 20220120 MGI PMID:33859201 11284 Selenow selenoprotein W gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20220120 MGI PMID:33859201 11284 Selenow selenoprotein W gene MP:0005605 increased bone mass IAGP N RGD:5509061 20220120 MGI PMID:33859201 11284 Selenow selenoprotein W gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20220120 MGI PMID:33859201 11284 Selenow selenoprotein W gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20220120 MGI PMID:33859201 11284 Selenow selenoprotein W gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20220120 MGI PMID:33859201 11284 Selenow selenoprotein W gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20220120 MGI PMID:33859201 11284 Selenow selenoprotein W gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20220120 MGI PMID:33859201 11285 Mapk10 mitogen-activated protein kinase 10 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:17174920 11285 Mapk10 mitogen-activated protein kinase 10 gene MP:0001051 abnormal somatic motor system morphology IAGP N RGD:5509061 20141003 MGI PMID:15528206 11285 Mapk10 mitogen-activated protein kinase 10 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:14704277 11285 Mapk10 mitogen-activated protein kinase 10 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:14704277 11285 Mapk10 mitogen-activated protein kinase 10 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:9349820 11285 Mapk10 mitogen-activated protein kinase 10 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11567045 11285 Mapk10 mitogen-activated protein kinase 10 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:9349820 11285 Mapk10 mitogen-activated protein kinase 10 gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:14704277 11287 Sftpd surfactant associated protein D gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11698462 11287 Sftpd surfactant associated protein D gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12376353 11287 Sftpd surfactant associated protein D gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:10801980 11287 Sftpd surfactant associated protein D gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12376353 11287 Sftpd surfactant associated protein D gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:9751757 11287 Sftpd surfactant associated protein D gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:9774472 11287 Sftpd surfactant associated protein D gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:10801980 11287 Sftpd surfactant associated protein D gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:12376353 11287 Sftpd surfactant associated protein D gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:15310555 11287 Sftpd surfactant associated protein D gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:10801980 11287 Sftpd surfactant associated protein D gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:15310555 11287 Sftpd surfactant associated protein D gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:16500946 11287 Sftpd surfactant associated protein D gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:9751757 11287 Sftpd surfactant associated protein D gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:9774472 11287 Sftpd surfactant associated protein D gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10801980 11287 Sftpd surfactant associated protein D gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11698462 11287 Sftpd surfactant associated protein D gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:10801980 11287 Sftpd surfactant associated protein D gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:9774472 11287 Sftpd surfactant associated protein D gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20141003 MGI PMID:10801980 11287 Sftpd surfactant associated protein D gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:10801980 11287 Sftpd surfactant associated protein D gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:15310555 11287 Sftpd surfactant associated protein D gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9774472 11287 Sftpd surfactant associated protein D gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12376353 11287 Sftpd surfactant associated protein D gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:9751757 11287 Sftpd surfactant associated protein D gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:9774472 11287 Sftpd surfactant associated protein D gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:10801980 11287 Sftpd surfactant associated protein D gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:9774472 11287 Sftpd surfactant associated protein D gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10801980 11287 Sftpd surfactant associated protein D gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15310555 11287 Sftpd surfactant associated protein D gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:11698462 11287 Sftpd surfactant associated protein D gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10801980 11287 Sftpd surfactant associated protein D gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:12376353 11287 Sftpd surfactant associated protein D gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:11698462 11287 Sftpd surfactant associated protein D gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:15310555 11287 Sftpd surfactant associated protein D gene MP:0004781 abnormal surfactant composition IAGP N RGD:5509061 20141003 MGI PMID:11698462 11287 Sftpd surfactant associated protein D gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20141003 MGI PMID:15310555 11287 Sftpd surfactant associated protein D gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9751757 11287 Sftpd surfactant associated protein D gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:10801980 11287 Sftpd surfactant associated protein D gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:9774472 11287 Sftpd surfactant associated protein D gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10801980 11287 Sftpd surfactant associated protein D gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:12376353 11287 Sftpd surfactant associated protein D gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:15310555 11287 Sftpd surfactant associated protein D gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:9751757 11287 Sftpd surfactant associated protein D gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:9774472 11287 Sftpd surfactant associated protein D gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:10801980 11287 Sftpd surfactant associated protein D gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:11698462 11287 Sftpd surfactant associated protein D gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:11698462 11287 Sftpd surfactant associated protein D gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:15310555 11287 Sftpd surfactant associated protein D gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:9751757 11287 Sftpd surfactant associated protein D gene MP:0010815 enlarged alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:15310555 11287 Sftpd surfactant associated protein D gene MP:0010815 enlarged alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:9751757 11287 Sftpd surfactant associated protein D gene MP:0010898 abnormal pulmonary alveolus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12376353 11287 Sftpd surfactant associated protein D gene MP:0010898 abnormal pulmonary alveolus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15310555 11287 Sftpd surfactant associated protein D gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:11698462 11290 Shox2 SHOX homeobox 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:16537395 11290 Shox2 SHOX homeobox 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16141225 11290 Shox2 SHOX homeobox 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:17372176 11290 Shox2 SHOX homeobox 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:16537395 11290 Shox2 SHOX homeobox 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16141225 11290 Shox2 SHOX homeobox 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:21454626 11290 Shox2 SHOX homeobox 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:17372176 11290 Shox2 SHOX homeobox 2 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:16537395 11290 Shox2 SHOX homeobox 2 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16537395 11290 Shox2 SHOX homeobox 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16537395 11290 Shox2 SHOX homeobox 2 gene MP:0003228 abnormal sinus venosus morphology IAGP N RGD:5509061 20141003 MGI PMID:17372176 11290 Shox2 SHOX homeobox 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:24267650 11290 Shox2 SHOX homeobox 2 gene MP:0003854 abnormal forelimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:16537395 11290 Shox2 SHOX homeobox 2 gene MP:0003856 abnormal hindlimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:16537395 11290 Shox2 SHOX homeobox 2 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:16537395 11290 Shox2 SHOX homeobox 2 gene MP:0004349 absent femur IAGP N RGD:5509061 20141003 MGI PMID:16537395 11290 Shox2 SHOX homeobox 2 gene MP:0004352 absent humerus IAGP N RGD:5509061 20141003 MGI PMID:16537395 11290 Shox2 SHOX homeobox 2 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:16537395 11290 Shox2 SHOX homeobox 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:21454626 11290 Shox2 SHOX homeobox 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21454626 11290 Shox2 SHOX homeobox 2 gene MP:0008503 abnormal spinal cord grey matter morphology IAGP N RGD:5509061 20141003 MGI PMID:24267650 11290 Shox2 SHOX homeobox 2 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141003 MGI PMID:16141225 11290 Shox2 SHOX homeobox 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:21454626 11290 Shox2 SHOX homeobox 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:21454626 11290 Shox2 SHOX homeobox 2 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:16141225 11290 Shox2 SHOX homeobox 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16141225 11290 Shox2 SHOX homeobox 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 11290 Shox2 SHOX homeobox 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21454626 11290 Shox2 SHOX homeobox 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21454626 11290 Shox2 SHOX homeobox 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17372176 11290 Shox2 SHOX homeobox 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23620086 11290 Shox2 SHOX homeobox 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11290 Shox2 SHOX homeobox 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16141225 11290 Shox2 SHOX homeobox 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23620086 11290 Shox2 SHOX homeobox 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23620086 11290 Shox2 SHOX homeobox 2 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 11290 Shox2 SHOX homeobox 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20240523 MGI 11290 Shox2 SHOX homeobox 2 gene MP:0021214 anterior cleft palate IAGP N RGD:5509061 20221201 MGI PMID:16141225 11290 Shox2 SHOX homeobox 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:16141225 11290 Shox2 SHOX homeobox 2 gene MP:0030330 abnormal temporomandibular joint disk morphology IAGP N RGD:5509061 20171109 MGI PMID:21454626 11290 Shox2 SHOX homeobox 2 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:16141225 11290 Shox2 SHOX homeobox 2 gene MP:0031542 sinoatrial node hypoplasia IAGP N RGD:5509061 20240104 MGI PMID:23620086 11291488 Trbv13-2 T cell receptor beta, variable 13-2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20160630 MGI PMID:17410206 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20210520 MGI 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210429 MGI PMID:25641256 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210520 MGI 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20210429 MGI PMID:25641256 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20210429 MGI PMID:25641256 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20210429 MGI PMID:25641256 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20210429 MGI PMID:25641256 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20210520 MGI 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20210429 MGI PMID:25641256 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20210429 MGI PMID:25641256 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20210429 MGI PMID:25641256 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20210429 MGI PMID:25641256 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20210520 MGI 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20210429 MGI PMID:25641256 11295 Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210429 MGI PMID:25641256 11295908 Igha immunoglobulin heavy constant alpha gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160630 MGI PMID:15199411 11295908 Igha immunoglobulin heavy constant alpha gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160630 MGI PMID:20956327 11295908 Igha immunoglobulin heavy constant alpha gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20160630 MGI PMID:10072491 11295908 Igha immunoglobulin heavy constant alpha gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20160630 MGI PMID:11123296 11295908 Igha immunoglobulin heavy constant alpha gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20160630 MGI PMID:10072491 11295908 Igha immunoglobulin heavy constant alpha gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20160630 MGI PMID:15199411 11295908 Igha immunoglobulin heavy constant alpha gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20160630 MGI PMID:15199411 11295908 Igha immunoglobulin heavy constant alpha gene MP:0002083 premature death IAGP N RGD:5509061 20160630 MGI PMID:20956327 11295908 Igha immunoglobulin heavy constant alpha gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20160630 MGI PMID:11123296 11295908 Igha immunoglobulin heavy constant alpha gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20160630 MGI PMID:15199411 11295908 Igha immunoglobulin heavy constant alpha gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20160630 MGI PMID:11123296 11295908 Igha immunoglobulin heavy constant alpha gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20160630 MGI PMID:10072491 11295908 Igha immunoglobulin heavy constant alpha gene MP:0002493 increased IgG level IAGP N RGD:5509061 20160630 MGI PMID:10072491 11295908 Igha immunoglobulin heavy constant alpha gene MP:0002493 increased IgG level IAGP N RGD:5509061 20160630 MGI PMID:15199411 11295908 Igha immunoglobulin heavy constant alpha gene MP:0002494 increased IgM level IAGP N RGD:5509061 20160630 MGI PMID:10072491 11295908 Igha immunoglobulin heavy constant alpha gene MP:0002494 increased IgM level IAGP N RGD:5509061 20160630 MGI PMID:11123296 11295908 Igha immunoglobulin heavy constant alpha gene MP:0002494 increased IgM level IAGP N RGD:5509061 20160630 MGI PMID:15199411 11295908 Igha immunoglobulin heavy constant alpha gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20160630 MGI PMID:8567970 11295908 Igha immunoglobulin heavy constant alpha gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20160630 MGI PMID:20956327 11295908 Igha immunoglobulin heavy constant alpha gene MP:0005014 increased B cell number IAGP N RGD:5509061 20160630 MGI PMID:20956327 11295908 Igha immunoglobulin heavy constant alpha gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20160630 MGI PMID:11748158 11295908 Igha immunoglobulin heavy constant alpha gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20160630 MGI PMID:17056558 11295908 Igha immunoglobulin heavy constant alpha gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20160630 MGI PMID:11123296 11295908 Igha immunoglobulin heavy constant alpha gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20160630 MGI PMID:15199411 11295908 Igha immunoglobulin heavy constant alpha gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20160630 MGI PMID:11123296 11295908 Igha immunoglobulin heavy constant alpha gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20160630 MGI PMID:15199411 11295908 Igha immunoglobulin heavy constant alpha gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20160630 MGI PMID:20956327 11295908 Igha immunoglobulin heavy constant alpha gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20160630 MGI PMID:20956327 11295908 Igha immunoglobulin heavy constant alpha gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20160630 MGI PMID:10072491 11295908 Igha immunoglobulin heavy constant alpha gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:10072491 11295908 Igha immunoglobulin heavy constant alpha gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:11123296 11295908 Igha immunoglobulin heavy constant alpha gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20160630 MGI PMID:10072491 11295908 Igha immunoglobulin heavy constant alpha gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20160630 MGI PMID:10072491 11295908 Igha immunoglobulin heavy constant alpha gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20160630 MGI PMID:11123296 11295908 Igha immunoglobulin heavy constant alpha gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20160630 MGI PMID:10072491 11295908 Igha immunoglobulin heavy constant alpha gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20160630 MGI PMID:10072491 11295908 Igha immunoglobulin heavy constant alpha gene MP:0008781 abnormal B cell apoptosis IAGP N RGD:5509061 20160630 MGI PMID:15199411 11295908 Igha immunoglobulin heavy constant alpha gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20160630 MGI PMID:15199411 11295908 Igha immunoglobulin heavy constant alpha gene MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20160630 MGI PMID:15199411 11295908 Igha immunoglobulin heavy constant alpha gene MP:0010337 increased chronic lymphocytic leukemia incidence IAGP N RGD:5509061 20160630 MGI PMID:20956327 11295908 Igha immunoglobulin heavy constant alpha gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:15199411 11295908 Igha immunoglobulin heavy constant alpha gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:11123296 11296376 Ighd immunoglobulin heavy constant delta gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20160630 MGI PMID:8418208 11296376 Ighd immunoglobulin heavy constant delta gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20160630 MGI PMID:8446604 11296376 Ighd immunoglobulin heavy constant delta gene MP:0002490 abnormal immunoglobulin level IEA N RGD:5509061 20160630 MGI 11296376 Ighd immunoglobulin heavy constant delta gene MP:0002491 decreased IgD level IEA N RGD:5509061 20180215 MGI 11296376 Ighd immunoglobulin heavy constant delta gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20160630 MGI PMID:8418208 11296376 Ighd immunoglobulin heavy constant delta gene MP:0002495 increased IgA level IAGP N RGD:5509061 20160630 MGI PMID:8446604 11296376 Ighd immunoglobulin heavy constant delta gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160630 MGI PMID:8446604 11296376 Ighd immunoglobulin heavy constant delta gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20160630 MGI PMID:8446604 11296376 Ighd immunoglobulin heavy constant delta gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20160630 MGI PMID:8446604 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0000192 abnormal mineral level IAGP N RGD:5509061 20141003 MGI PMID:16807402 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:17264314 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:17264314 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:17264314 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0001771 abnormal circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:17215439 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17264314 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17264314 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:16807402 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:17215439 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:17264314 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0003028 alkalosis IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:17264314 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:17215439 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0003353 decreased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:16807402 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0003353 decreased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0003653 decreased skin turgor IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0005522 increased circulating atrial natriuretic factor IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:17264314 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0005557 increased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17264314 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17264314 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0005568 increased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0005582 increased renin activity IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0005633 increased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:17264314 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0008055 increased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0010092 increased circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:17215439 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0010108 abnormal renal water reabsorption IAGP N RGD:5509061 20141003 MGI PMID:17215439 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0011295 abnormal tubuloglomerular feedback response IAGP N RGD:5509061 20141003 MGI PMID:16807402 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0011296 decreased tubuloglomerular feedback response IAGP N RGD:5509061 20141003 MGI PMID:17215439 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20141003 MGI PMID:17264314 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0011403 pyelonephritis IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0011404 pyelitis IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0011424 decreased urine uric acid level IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0011435 increased urine magnesium level IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0011465 abnormal urine urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0011470 increased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:17264314 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0011563 increased urine prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:20219826 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20170921 MGI PMID:10779555 11297 Slc12a1 solute carrier family 12, member 1 gene MP:0031404 increased tubuloglomerular feedback response IAGP N RGD:5509061 20220630 MGI PMID:17215439 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:24367518 11299 Slc16a1 solute carrier family 16 (monocarboxylic acid transporters), member 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:24367518 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11463816 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9427250 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9427250 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19553450 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21814181 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17652604 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17898223 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19553450 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21814181 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9427251 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11463816 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:11463816 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:11463816 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20141003 MGI PMID:17307644 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20141003 MGI PMID:17898223 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:19553450 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9427251 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:9427251 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:17898223 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:19553450 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10521591 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9275230 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0002204 abnormal synaptic neurotransmitter level IAGP N RGD:5509061 20141003 MGI PMID:9427251 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:19553450 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:21814181 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:17898223 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:14980210 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003064 decreased coping response IAGP N RGD:5509061 20141003 MGI PMID:17898223 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003064 decreased coping response IAGP N RGD:5509061 20141003 MGI PMID:19553450 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:19553450 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:17652604 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:10521591 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15496457 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003444 abnormal neurotransmitter uptake IAGP N RGD:5509061 20141003 MGI PMID:9427251 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003462 abnormal response to novel odor IAGP N RGD:5509061 20141003 MGI PMID:19553450 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:17307644 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:19553450 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20141003 MGI PMID:19553450 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:17898223 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:11463816 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:19553450 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:9427250 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15496457 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:9427250 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:9427250 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:15496457 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:9427250 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:9427251 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:9427251 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:9427251 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:11463816 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:15496457 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:17652604 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:19553450 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:9427250 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:9427251 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20141003 MGI PMID:17652604 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:19553450 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9427251 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:9427250 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:9427251 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:17307644 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:9275230 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:9275230 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:9427251 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:9427251 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0009854 impaired gastric peristalsis IAGP N RGD:5509061 20141003 MGI PMID:19553450 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:11463816 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:19553450 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:21814181 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9275230 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9427250 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9427251 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21814181 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11463816 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9275230 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:17652604 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11463816 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:9275230 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0011479 abnormal catecholamine level IAGP N RGD:5509061 20141003 MGI PMID:21814181 11300 Slc18a2 solute carrier family 18 (vesicular monoamine), member 2 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:19553450 11301 Slc1a1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 gene MP:0001307 fused cornea and lens IEA N RGD:5509061 20201231 MGI 11301 Slc1a1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9233792 11301 Slc1a1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 11301 Slc1a1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20201022 MGI 11301 Slc1a1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 gene MP:0002944 increased lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:17607354 11301 Slc1a1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:15363892 11301 Slc1a1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 11301 Slc1a1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20141003 MGI PMID:17607354 11301 Slc1a1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:17607354 11301 Slc1a1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:17607354 11301 Slc1a1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 11301 Slc1a1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 gene MP:0030613 dicarboxylic aciduria IAGP N RGD:5509061 20180920 MGI PMID:9233792 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0000599 enlarged liver IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20231207 MGI PMID:32619424 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20160630 MGI PMID:23423996 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20160630 MGI PMID:22897848 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20160721 MGI PMID:26366712 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002083 premature death IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002083 premature death IAGP N RGD:5509061 20160630 MGI PMID:22897848 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002083 premature death IAGP N RGD:5509061 20160721 MGI PMID:26366712 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20231207 MGI PMID:32619424 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002440 abnormal memory B cell morphology IAGP N RGD:5509061 20160630 MGI PMID:16767092 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20160630 MGI PMID:9103199 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20160630 MGI PMID:23423996 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002494 increased IgM level IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002494 increased IgM level IAGP N RGD:5509061 20220616 MGI PMID:33343574 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002497 increased IgE level IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0002497 increased IgE level IAGP N RGD:5509061 20160630 MGI PMID:23423996 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20200402 MGI PMID:30287618 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20200402 MGI PMID:30287618 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200402 MGI PMID:30287618 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20210812 MGI PMID:33193409 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20220616 MGI PMID:33343574 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20160630 MGI PMID:16767092 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20160630 MGI PMID:22897848 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20160630 MGI PMID:7892607 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20160630 MGI PMID:8438159 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0005014 increased B cell number IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0005014 increased B cell number IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20160630 MGI PMID:23680150 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20160630 MGI PMID:23423996 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20160630 MGI PMID:23423996 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008094 absent memory B cells IAGP N RGD:5509061 20160630 MGI PMID:9103199 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20200402 MGI PMID:30287618 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20220616 MGI PMID:33343574 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20200402 MGI PMID:30287618 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008100 absent plasma cells IAGP N RGD:5509061 20160630 MGI PMID:16767092 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20200409 MGI PMID:30205047 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20160630 MGI PMID:22897848 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20160630 MGI PMID:23680150 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20190926 MGI PMID:30013024 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20200402 MGI PMID:30287618 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20200409 MGI PMID:30205047 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20220616 MGI PMID:33343574 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20160630 MGI PMID:22431510 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20160630 MGI PMID:23027924 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20160630 MGI PMID:23680150 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20200409 MGI PMID:30205047 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20160630 MGI PMID:23680150 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20160630 MGI PMID:23680150 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20160630 MGI PMID:23680150 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20160630 MGI PMID:23001146 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20160630 MGI PMID:23680150 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:16767092 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:23423996 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:23680150 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:7892607 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:8438159 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:9103199 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20160630 MGI PMID:23680150 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20160630 MGI PMID:23680150 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20200402 MGI PMID:30287618 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20160630 MGI PMID:23423996 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20160630 MGI PMID:23423996 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20160630 MGI PMID:21156282 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20210812 MGI PMID:33193409 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20220616 MGI PMID:33343574 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20160630 MGI PMID:23423996 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0009317 increased follicular lymphoma incidence IAGP N RGD:5509061 20160721 MGI PMID:26366712 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20160630 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20160630 MGI PMID:23423996 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20190926 MGI PMID:30013024 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:21339646 11302549 Ighg1 immunoglobulin heavy constant gamma 1 (G1m marker) gene MP:0020155 enhanced humoral immune response IAGP N RGD:5509061 20200402 MGI PMID:30287618 11303086 Ighm immunoglobulin heavy constant mu gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20160630 MGI PMID:17202317 11303086 Ighm immunoglobulin heavy constant mu gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20160630 MGI PMID:17202317 11303086 Ighm immunoglobulin heavy constant mu gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20160630 MGI PMID:17202317 11303086 Ighm immunoglobulin heavy constant mu gene MP:0000274 enlarged heart IAGP N RGD:5509061 20160630 MGI PMID:16751419 11303086 Ighm immunoglobulin heavy constant mu gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20160630 MGI PMID:15922720 11303086 Ighm immunoglobulin heavy constant mu gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20160630 MGI PMID:11884426 11303086 Ighm immunoglobulin heavy constant mu gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20160630 MGI PMID:15894265 11303086 Ighm immunoglobulin heavy constant mu gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20160630 MGI PMID:11733579 11303086 Ighm immunoglobulin heavy constant mu gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20160630 MGI PMID:15894265 11303086 Ighm immunoglobulin heavy constant mu gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20160630 MGI PMID:17899553 11303086 Ighm immunoglobulin heavy constant mu gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160630 MGI PMID:15894265 11303086 Ighm immunoglobulin heavy constant mu gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20160630 MGI PMID:11035071 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20160630 MGI PMID:11114377 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20200116 MGI PMID:16505059 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20160630 MGI PMID:22308431 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20160630 MGI PMID:15475246 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20160630 MGI PMID:9590224 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20160630 MGI PMID:11035071 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20160630 MGI PMID:9590224 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20160630 MGI PMID:11035071 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20160630 MGI PMID:1545868 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20160630 MGI PMID:15475246 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20160630 MGI PMID:1901381 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20160630 MGI PMID:11035071 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20160630 MGI PMID:11148220 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20160630 MGI PMID:11937563 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20160630 MGI PMID:18086860 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20160630 MGI PMID:19727123 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20160630 MGI PMID:11035071 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20160630 MGI PMID:11717190 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20160630 MGI PMID:12471099 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20160630 MGI PMID:1545868 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20160630 MGI PMID:18086860 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20160630 MGI PMID:9590224 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20160630 MGI PMID:9707605 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20160630 MGI PMID:19727123 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20160630 MGI PMID:15922720 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20160630 MGI PMID:10843660 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20160630 MGI PMID:15922720 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20160630 MGI PMID:22284419 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001853 heart inflammation IAGP N RGD:5509061 20160630 MGI PMID:16751419 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001856 myocarditis IAGP N RGD:5509061 20160630 MGI PMID:22284419 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20160630 MGI PMID:10748243 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20160630 MGI PMID:22284419 11303086 Ighm immunoglobulin heavy constant mu gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20160630 MGI PMID:16272283 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20160630 MGI PMID:15894265 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002083 premature death IAGP N RGD:5509061 20160630 MGI PMID:15894265 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002083 premature death IAGP N RGD:5509061 20160630 MGI PMID:15922720 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002083 premature death IAGP N RGD:5509061 20160630 MGI PMID:22284419 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20160630 MGI PMID:11937563 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20160630 MGI PMID:16272283 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20160630 MGI PMID:1545868 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20160630 MGI PMID:16204304 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20160630 MGI PMID:18086860 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20160630 MGI PMID:1901381 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20160630 MGI PMID:26832406 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160630 MGI PMID:10640761 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20160630 MGI PMID:17899553 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20160630 MGI PMID:17899553 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20160630 MGI PMID:15894265 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20160630 MGI PMID:9590224 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20160630 MGI PMID:17899553 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002363 abnormal spleen marginal sinus morphology IAGP N RGD:5509061 20160630 MGI PMID:15004164 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002453 abnormal B lymphocyte antigen presentation IAGP N RGD:5509061 20160630 MGI PMID:12516557 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20160630 MGI PMID:9590224 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20160630 MGI PMID:11035071 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20160630 MGI PMID:15475246 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20160630 MGI PMID:15894265 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20160630 MGI PMID:21987785 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002473 impaired complement classical pathway IAGP N RGD:5509061 20160630 MGI PMID:21987785 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20160630 MGI PMID:11035071 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20160630 MGI PMID:11937563 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002494 increased IgM level IAGP N RGD:5509061 20160630 MGI PMID:11148220 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002495 increased IgA level IAGP N RGD:5509061 20160630 MGI PMID:9590224 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002704 tubular nephritis IAGP N RGD:5509061 20160630 MGI PMID:22284419 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20160630 MGI PMID:21987785 11303086 Ighm immunoglobulin heavy constant mu gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20160630 MGI PMID:11035071 11303086 Ighm immunoglobulin heavy constant mu gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20160630 MGI PMID:11067910 11303086 Ighm immunoglobulin heavy constant mu gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20160630 MGI PMID:22284419 11303086 Ighm immunoglobulin heavy constant mu gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20160630 MGI PMID:21683627 11303086 Ighm immunoglobulin heavy constant mu gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20160630 MGI PMID:12486099 11303086 Ighm immunoglobulin heavy constant mu gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20160630 MGI PMID:20111715 11303086 Ighm immunoglobulin heavy constant mu gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20160630 MGI PMID:10748243 11303086 Ighm immunoglobulin heavy constant mu gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20160630 MGI PMID:11035071 11303086 Ighm immunoglobulin heavy constant mu gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20160630 MGI PMID:17202317 11303086 Ighm immunoglobulin heavy constant mu gene MP:0003901 abnormal PR interval IAGP N RGD:5509061 20160630 MGI PMID:16751419 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004031 insulitis IAGP N RGD:5509061 20160630 MGI PMID:11698422 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004031 insulitis IAGP N RGD:5509061 20160630 MGI PMID:12516557 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004031 insulitis IAGP N RGD:5509061 20160630 MGI PMID:15448087 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20160630 MGI PMID:10748243 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20180111 MGI PMID:24078696 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20160630 MGI PMID:11698422 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20160630 MGI PMID:15448087 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20160630 MGI PMID:8920894 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20160630 MGI PMID:12516557 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20160630 MGI PMID:8920894 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20160630 MGI PMID:11148220 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20160630 MGI PMID:21378751 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20160630 MGI PMID:11733579 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20160630 MGI PMID:11717190 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20160630 MGI PMID:9590224 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20160630 MGI PMID:20111715 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005014 increased B cell number IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005015 increased T cell number IAGP N RGD:5509061 20160630 MGI PMID:11035071 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160630 MGI PMID:16204304 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160630 MGI PMID:21378751 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005022 abnormal immature B cell morphology IAGP N RGD:5509061 20160630 MGI PMID:9707605 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20160630 MGI PMID:16272283 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20160630 MGI PMID:11748158 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20160630 MGI PMID:20664169 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20160630 MGI PMID:11717190 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20160630 MGI PMID:12516557 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20160630 MGI PMID:10843660 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005150 cachexia IAGP N RGD:5509061 20160630 MGI PMID:15922720 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20160630 MGI PMID:15894265 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20160630 MGI PMID:22308431 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20160630 MGI PMID:10843380 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20160630 MGI PMID:10843660 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20160630 MGI PMID:11698422 11303086 Ighm immunoglobulin heavy constant mu gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20160630 MGI PMID:10843660 11303086 Ighm immunoglobulin heavy constant mu gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20160630 MGI PMID:12516557 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008071 absent B cells IAGP N RGD:5509061 20160630 MGI PMID:12516557 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20160630 MGI PMID:11067910 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20160630 MGI PMID:11733579 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20160630 MGI PMID:11733579 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20160630 MGI PMID:12516557 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20160630 MGI PMID:15894265 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20160630 MGI PMID:11733579 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008164 abnormal B-1a B cell morphology IAGP N RGD:5509061 20160630 MGI PMID:12471099 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008164 abnormal B-1a B cell morphology IAGP N RGD:5509061 20160630 MGI PMID:9707605 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20160630 MGI PMID:12516557 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20160630 MGI PMID:9707605 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20160630 MGI PMID:12471099 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20160630 MGI PMID:12471099 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20160630 MGI PMID:21378751 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008198 abnormal follicular dendritic cell antigen presentation IAGP N RGD:5509061 20160630 MGI PMID:9590224 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008201 absent follicular dendritic cells IAGP N RGD:5509061 20160630 MGI PMID:15004164 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20160630 MGI PMID:21378751 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20160630 MGI PMID:11035071 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20160630 MGI PMID:11717190 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20160630 MGI PMID:1545868 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20160630 MGI PMID:15475246 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008213 absent immature B cells IAGP N RGD:5509061 20160630 MGI PMID:1545868 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20160630 MGI PMID:11717190 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20160630 MGI PMID:11717190 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008240 abnormal spleen marginal zone macrophage morphology IAGP N RGD:5509061 20160630 MGI PMID:15004164 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008241 abnormal metallophilic macrophage morphology IAGP N RGD:5509061 20160630 MGI PMID:15004164 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008241 abnormal metallophilic macrophage morphology IAGP N RGD:5509061 20160630 MGI PMID:17899553 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008401 abnormal CD8 positive, alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20160630 MGI PMID:11884426 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200116 MGI PMID:16505059 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20160630 MGI PMID:15894265 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20160630 MGI PMID:17899553 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20160630 MGI PMID:15894265 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20160630 MGI PMID:15894265 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:11148220 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:11937563 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:9590224 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160630 MGI PMID:9707605 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20160630 MGI PMID:11148220 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20160630 MGI PMID:9590224 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20160630 MGI PMID:11148220 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20160630 MGI PMID:20133609 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20160630 MGI PMID:9590224 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20160630 MGI PMID:9590224 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20160630 MGI PMID:9707605 11303086 Ighm immunoglobulin heavy constant mu gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20160630 MGI PMID:12471099 11303086 Ighm immunoglobulin heavy constant mu gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20160630 MGI PMID:17202317 11303086 Ighm immunoglobulin heavy constant mu gene MP:0010965 decreased compact bone volume IAGP N RGD:5509061 20160630 MGI PMID:17202317 11303086 Ighm immunoglobulin heavy constant mu gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160630 MGI PMID:12516557 11303086 Ighm immunoglobulin heavy constant mu gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160630 MGI PMID:22608497 11303086 Ighm immunoglobulin heavy constant mu gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:12516557 11303086 Ighm immunoglobulin heavy constant mu gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:9655395 11303386 Igkj1 immunoglobulin kappa joining 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160630 MGI PMID:15242641 11303386 Igkj1 immunoglobulin kappa joining 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20160630 MGI PMID:16703567 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23549084 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9354799 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20097878 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:9354799 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23549084 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9354799 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23549084 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9354799 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:9354799 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9354799 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:23549084 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0003926 decreased cellular glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:23549084 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:23549084 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:9354799 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:9354799 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:9354799 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23549084 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23549084 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0006353 increased glycosylated hemoglobin level IEA N RGD:5509061 20211021 MGI 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:9354799 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0009109 decreased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:9354799 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20180614 MGI PMID:9354799 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23549084 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23549084 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:23549084 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:20097878 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9354799 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0030589 increased pancreatic alpha cell mass IAGP N RGD:5509061 20180614 MGI PMID:9354799 11306 Slc2a2 solute carrier family 2 (facilitated glucose transporter), member 2 gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:23549084 11307 Slc2a3 solute carrier family 2 (facilitated glucose transporter), member 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18780771 11307 Slc2a3 solute carrier family 2 (facilitated glucose transporter), member 3 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18780771 11307 Slc2a3 solute carrier family 2 (facilitated glucose transporter), member 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17213475 11307 Slc2a3 solute carrier family 2 (facilitated glucose transporter), member 3 gene MP:0004265 abnormal placental transport IAGP N RGD:5509061 20141003 MGI PMID:17213475 11307 Slc2a3 solute carrier family 2 (facilitated glucose transporter), member 3 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:18780771 11307 Slc2a3 solute carrier family 2 (facilitated glucose transporter), member 3 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:18780771 11307 Slc2a3 solute carrier family 2 (facilitated glucose transporter), member 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17213475 11307 Slc2a3 solute carrier family 2 (facilitated glucose transporter), member 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17213475 11307 Slc2a3 solute carrier family 2 (facilitated glucose transporter), member 3 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21316350 11308558 Ighe Immunoglobulin heavy constant epsilon gene MP:0002492 decreased IgE level IEA N RGD:5509061 20190103 MGI 11308830 Trgc1 T cell receptor gamma, constant 1 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20160630 MGI PMID:15345225 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:23341620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:23341620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:15123620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23341620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:23341620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15123620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15123620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:14673081 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15123620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:15123620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:23341620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14673081 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15123620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14673081 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14673081 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14673081 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15123620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15123620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:15123620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14673081 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:14673081 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:14673081 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0002661 abnormal corpus epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:14673081 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:14673081 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23341620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15123620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15123620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:23341620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:14673081 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20141003 MGI PMID:14673081 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:23341620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0008003 achlorhydria IAGP N RGD:5509061 20141003 MGI PMID:15123620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23341620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15123620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23341620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:23341620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15123620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15123620 11311 Slc4a2 solute carrier family 4 (anion exchanger), member 2 gene MP:0013566 dilated gastric gland IAGP N RGD:5509061 20150312 MGI PMID:15123620 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22124465 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22124465 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:22124465 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22124465 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0004348 long femur IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:22124465 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22124465 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0009480 distended cecum IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:22124465 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22124465 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0011435 increased urine magnesium level IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0011447 abnormal renal glucose reabsorption IAGP N RGD:5509061 20141003 MGI PMID:22124465 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0011466 increased urine urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0011923 abnormal bladder urine volume IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313 Slc5a1 solute carrier family 5 (sodium/glucose cotransporter), member 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:23149623 11313297 Trbv14 T cell receptor beta, variable 14 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20160630 MGI PMID:15282302 11313684 Traj18 T cell receptor alpha joining 18 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20181115 MGI PMID:28986544 11313684 Traj18 T cell receptor alpha joining 18 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20160818 MGI PMID:26075912 11313684 Traj18 T cell receptor alpha joining 18 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20181115 MGI PMID:28986544 11313684 Traj18 T cell receptor alpha joining 18 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20181115 MGI PMID:28986544 11313684 Traj18 T cell receptor alpha joining 18 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20181115 MGI PMID:28986544 11313684 Traj18 T cell receptor alpha joining 18 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20181115 MGI PMID:28986544 11313684 Traj18 T cell receptor alpha joining 18 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20181115 MGI PMID:28986544 11313684 Traj18 T cell receptor alpha joining 18 gene MP:0008041 absent NK T cells IAGP N RGD:5509061 20160818 MGI PMID:26075912 11313684 Traj18 T cell receptor alpha joining 18 gene MP:0008041 absent NK T cells IAGP N RGD:5509061 20181115 MGI PMID:28986544 11313684 Traj18 T cell receptor alpha joining 18 gene MP:0008559 abnormal interferon-gamma secretion IAGP N RGD:5509061 20160818 MGI PMID:26075912 11313684 Traj18 T cell receptor alpha joining 18 gene MP:0008601 abnormal circulating interleukin-4 level IAGP N RGD:5509061 20160818 MGI PMID:26075912 11313684 Traj18 T cell receptor alpha joining 18 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20181115 MGI PMID:28986544 11313684 Traj18 T cell receptor alpha joining 18 gene MP:0010936 decreased airway resistance IAGP N RGD:5509061 20160818 MGI PMID:26075912 11313684 Traj18 T cell receptor alpha joining 18 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20181115 MGI PMID:28986544 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10841514 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16380550 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:19208814 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:10841514 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20190718 MGI PMID:27111230 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20190718 MGI PMID:27111230 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20190718 MGI PMID:27111230 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:19208814 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:19016890 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20190718 MGI PMID:22431635 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:14625138 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16873667 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21814181 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:9547354 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21814181 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9547354 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20190718 MGI PMID:22431635 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:14625138 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:11320258 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:16542782 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20190718 MGI PMID:22431635 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12598736 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20190718 MGI PMID:27111230 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11320258 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10565817 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20141003 MGI PMID:14625138 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18599790 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12634480 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15763133 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:19208814 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20190718 MGI PMID:22431635 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:21814181 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:16542782 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0002635 reduced sensorimotor gating IAGP N RGD:5509061 20141003 MGI PMID:19208814 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20141003 MGI PMID:12533631 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:16380550 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0002798 abnormal active avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:14625138 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16380550 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19646988 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20190718 MGI PMID:27111230 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20190718 MGI PMID:27111230 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0003444 abnormal neurotransmitter uptake IAGP N RGD:5509061 20190718 MGI PMID:22431635 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:16542782 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0003877 abnormal serotonergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:14625138 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0003958 heart valve hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16380550 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0003989 abnormal barrel cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11517274 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:11320258 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18599790 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21282638 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20190718 MGI PMID:27111230 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16380550 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:10841514 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:18599790 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:11320258 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:14625138 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:18599790 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20190718 MGI PMID:27111230 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0006002 abnormal small intestinal transit time IAGP N RGD:5509061 20190718 MGI PMID:27111230 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0006276 abnormal autonomic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18599790 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20190718 MGI PMID:27111230 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20190718 MGI PMID:27111230 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18599790 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20190718 MGI PMID:22431635 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21282638 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:19208814 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:11320258 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0009713 enhanced conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:9636213 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20190718 MGI PMID:22431635 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21282638 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20190718 MGI PMID:22431635 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:21814181 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:10841514 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:16380550 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:9547354 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20190718 MGI PMID:27111230 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0010758 increased right ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:10841514 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0011082 abnormal gastrointestinal motility IAGP N RGD:5509061 20190718 MGI PMID:27111230 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19646988 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21814181 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0011479 abnormal catecholamine level IAGP N RGD:5509061 20141003 MGI PMID:21814181 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20190718 MGI PMID:27111230 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20190718 MGI PMID:22431635 11314 Slc6a4 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20190718 MGI PMID:22431635 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:17227870 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17227870 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:22841315 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0000836 abnormal substantia nigra morphology IAGP N RGD:5509061 20141003 MGI PMID:22131425 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:19750226 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9247269 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160623 MGI PMID:27038906 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21768369 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12617953 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20016108 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:8628395 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:21768369 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16754872 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19750538 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20016108 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21743470 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21795541 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22841315 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23152632 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17065462 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17227870 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20016108 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22841315 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160623 MGI PMID:27038906 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12617953 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22131425 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150827 MGI PMID:25915474 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160623 MGI PMID:27038906 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22841315 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:12617953 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:15710042 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:20016108 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:11172062 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:11320258 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17227870 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:22131425 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001440 abnormal grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:15710042 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:9888856 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18701073 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20201029 MGI PMID:31365862 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11320258 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8628395 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9247269 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001746 abnormal pituitary secretion IAGP N RGD:5509061 20141003 MGI PMID:9247269 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:11172062 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:16950153 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:19750226 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22841315 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20150723 MGI PMID:25331903 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20180927 MGI PMID:16754872 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20170309 MGI PMID:26377476 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20160623 MGI PMID:27038906 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17227870 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22841315 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8628395 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20201022 MGI 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15763133 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16865686 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19666516 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22267337 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20150827 MGI PMID:25915474 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:22034972 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20150827 MGI PMID:25915474 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20180405 MGI PMID:29180115 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:9247269 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20180405 MGI PMID:29180115 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:11172062 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20240523 MGI 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12617953 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:20016108 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20150723 MGI PMID:25331903 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20160623 MGI PMID:27038906 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:12617953 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21743470 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21768369 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23152632 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18701073 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20223200 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21743470 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22034972 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20150723 MGI PMID:25331903 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:14980210 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20150827 MGI PMID:25915474 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20150827 MGI PMID:25915474 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:20016108 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:23152632 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20150402 MGI PMID:25609609 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16754872 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17227870 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19750226 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20016108 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20223200 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:17227870 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:21768369 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:22841315 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20150326 MGI PMID:25068655 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20150402 MGI PMID:25609609 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20160623 MGI PMID:27038906 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16754872 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003348 hypopituitarism IAGP N RGD:5509061 20141003 MGI PMID:9247269 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003444 abnormal neurotransmitter uptake IAGP N RGD:5509061 20141003 MGI PMID:16754872 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:11172062 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003462 abnormal response to novel odor IAGP N RGD:5509061 20141003 MGI PMID:16765459 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:21743470 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:19750226 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:20016108 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:22131425 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:11172062 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:19750226 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:22131425 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:21768369 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:11320258 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9247269 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:17227870 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:17227870 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:9247269 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18701073 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:21768369 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20150827 MGI PMID:25915474 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20150723 MGI PMID:25331903 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:16950153 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20150723 MGI PMID:24332984 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20150723 MGI PMID:25331903 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20150827 MGI PMID:25915474 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:11320258 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:16950153 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20150402 MGI PMID:25609609 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005603 neuron hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19750226 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160421 MGI 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:10564358 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:17227870 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:20016108 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:20223200 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22131425 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22143804 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22841315 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:23152632 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:8628395 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:9247269 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:9520487 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20150326 MGI PMID:25068655 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20150402 MGI PMID:25609609 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20150827 MGI PMID:25915474 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20160623 MGI PMID:27038906 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:9247269 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:22859504 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20150402 MGI PMID:25609609 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:21768369 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20150402 MGI PMID:25609609 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20150402 MGI PMID:25609609 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20150827 MGI PMID:25915474 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008329 decreased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9247269 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008332 decreased lactotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9247269 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008365 adenohypophysis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9247269 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008369 pituitary intermediate lobe hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9247269 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:22131425 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20150402 MGI PMID:25609609 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20150827 MGI PMID:25915474 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:22131425 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20150827 MGI PMID:25915474 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20160623 MGI PMID:27038906 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20160623 MGI PMID:27038906 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11172062 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21743470 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21743470 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20150723 MGI PMID:25331903 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21743470 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008918 microgliosis IAGP N RGD:5509061 20160623 MGI PMID:27038906 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22841315 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22841315 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20150827 MGI PMID:25915474 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:11320258 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:16754872 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:18701073 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:21795541 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19750226 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20150723 MGI PMID:25331903 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:18701073 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20141003 MGI PMID:21795541 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:21743470 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0009756 impaired behavioral response to nicotine IAGP N RGD:5509061 20141003 MGI PMID:21795541 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:20223200 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21057506 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:22131425 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20150723 MGI PMID:25331903 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180927 MGI PMID:20016108 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20141003 MGI PMID:21743470 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20141003 MGI PMID:21795541 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20141003 MGI PMID:22841315 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20150723 MGI PMID:25331903 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20170309 MGI PMID:26377476 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20180927 MGI PMID:16754872 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0010249 lactation failure IAGP N RGD:5509061 20150611 MGI PMID:9247269 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20150723 MGI PMID:24332984 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20016108 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:10564358 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:12617953 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:21057506 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20160623 MGI PMID:27038906 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:21057506 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:21057506 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:22143804 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20150402 MGI PMID:25609609 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20150402 MGI PMID:25609609 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0011975 neuronal cytoplasmic inclusions IAGP N RGD:5509061 20150402 MGI PMID:25609609 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0013218 abnormal substantia nigra pars reticulata morphology IAGP N RGD:5509061 20141003 MGI PMID:19750226 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20141003 MGI PMID:19750226 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20141003 MGI PMID:22914740 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20141003 MGI PMID:23152632 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:25915474 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0014373 increased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:18701073 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0014375 increased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:18701073 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0014381 abnormal miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:22034972 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:27038906 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0030610 absent teeth IEA N RGD:5509061 20201022 MGI 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:11172062 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:12617953 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:16436185 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22034972 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:25915474 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:8628395 11315 Slc6a3 solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:9888856 11315710 Trav1 T cell receptor alpha variable 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 11316 Slc7a1 solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9106662 11316 Slc7a1 solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9106662 11316 Slc7a1 solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9106662 11316 Slc7a1 solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:9106662 11316 Slc7a1 solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 gene MP:0002424 abnormal reticulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9106662 11316 Slc7a1 solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:9106662 11316 Slc7a1 solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:9106662 11316 Slc7a1 solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9106662 11316 Slc7a1 solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:9106662 11316 Slc7a1 solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9106662 11316 Slc7a1 solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9106662 11316 Slc7a1 solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9106662 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10199808 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:11358967 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:23904602 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:10199808 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:10199808 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:10199808 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10199808 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10199808 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:10199808 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0001443 poor grooming IAGP N RGD:5509061 20141003 MGI PMID:10199808 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:10199808 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12970112 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:12970112 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:23904602 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:23904602 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0008035 behavioral arrest IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20221215 MGI 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:23904602 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0009979 abnormal cerebellum deep nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0009980 abnormal cerebellum dentate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10199808 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9335342 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0013532 abnormal parotid gland physiology IAGP N RGD:5509061 20160310 MGI PMID:11358967 11317 Slc9a1 solute carrier family 9 (sodium/hydrogen exchanger), member 1 gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:23904602 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0008728 increased memory B cell number IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0008729 decreased memory B cell number IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0008896 increased IgG2c level IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20241031 MGI PMID:35133976 11317092 Ighg2c immunoglobulin heavy constant gamma 2C gene MP:0013654 increased CD103-positive CD11b-low dendritic cell number IAGP N RGD:5509061 20241031 MGI PMID:35133976 11318 Slc9a2 solute carrier family 9 (sodium/hydrogen exchanger), member 2 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11099134 11318 Slc9a2 solute carrier family 9 (sodium/hydrogen exchanger), member 2 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9502765 11318 Slc9a2 solute carrier family 9 (sodium/hydrogen exchanger), member 2 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:11099134 11318 Slc9a2 solute carrier family 9 (sodium/hydrogen exchanger), member 2 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:9502765 11318 Slc9a2 solute carrier family 9 (sodium/hydrogen exchanger), member 2 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9502765 11318 Slc9a2 solute carrier family 9 (sodium/hydrogen exchanger), member 2 gene MP:0008001 hypochlorhydria IAGP N RGD:5509061 20141003 MGI PMID:9502765 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20240523 MGI 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0000466 esophageal epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9662405 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9662405 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0000525 renal tubular acidosis IAGP N RGD:5509061 20141003 MGI PMID:9662405 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:9662405 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:9662405 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11698654 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:9662405 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:9662405 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0003027 abnormal blood pH regulation IAGP N RGD:5509061 20141003 MGI PMID:9662405 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:9662405 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0006423 dilated rete testis IAGP N RGD:5509061 20141003 MGI PMID:11698654 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0009140 dilated efferent ductule of testis IAGP N RGD:5509061 20141003 MGI PMID:11698654 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0009480 distended cecum IAGP N RGD:5509061 20141003 MGI PMID:9662405 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:9662405 11319 Slc9a3 solute carrier family 9 (sodium/hydrogen exchanger), member 3 gene MP:0010108 abnormal renal water reabsorption IAGP N RGD:5509061 20141003 MGI PMID:9662405 11320 Slc9a4 solute carrier family 9 (sodium/hydrogen exchanger), member 4 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160421 MGI 11320 Slc9a4 solute carrier family 9 (sodium/hydrogen exchanger), member 4 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15684419 11320 Slc9a4 solute carrier family 9 (sodium/hydrogen exchanger), member 4 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20160421 MGI 11320 Slc9a4 solute carrier family 9 (sodium/hydrogen exchanger), member 4 gene MP:0001653 gastric necrosis IAGP N RGD:5509061 20141003 MGI PMID:15684419 11320 Slc9a4 solute carrier family 9 (sodium/hydrogen exchanger), member 4 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:15684419 11320 Slc9a4 solute carrier family 9 (sodium/hydrogen exchanger), member 4 gene MP:0004138 abnormal mucous neck cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15684419 11320 Slc9a4 solute carrier family 9 (sodium/hydrogen exchanger), member 4 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15684419 11320 Slc9a4 solute carrier family 9 (sodium/hydrogen exchanger), member 4 gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15684419 11320 Slc9a4 solute carrier family 9 (sodium/hydrogen exchanger), member 4 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 11320 Slc9a4 solute carrier family 9 (sodium/hydrogen exchanger), member 4 gene MP:0008001 hypochlorhydria IAGP N RGD:5509061 20141003 MGI PMID:15684419 11320 Slc9a4 solute carrier family 9 (sodium/hydrogen exchanger), member 4 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 11320 Slc9a4 solute carrier family 9 (sodium/hydrogen exchanger), member 4 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160421 MGI 11320 Slc9a4 solute carrier family 9 (sodium/hydrogen exchanger), member 4 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:15684419 11321 Snai2 snail family zinc finger 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:17376812 11321 Snai2 snail family zinc finger 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17376812 11321 Snai2 snail family zinc finger 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20150409 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 11321 Snai2 snail family zinc finger 2 gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20150903 MGI PMID:18663143 11321 Snai2 snail family zinc finger 2 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20230601 MGI 11321 Snai2 snail family zinc finger 2 gene MP:0000370 head blaze IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 11321 Snai2 snail family zinc finger 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:17376812 11321 Snai2 snail family zinc finger 2 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 11321 Snai2 snail family zinc finger 2 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 11321 Snai2 snail family zinc finger 2 gene MP:0000692 small spleen IAGP N RGD:5509061 20150409 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20150409 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16801545 11321 Snai2 snail family zinc finger 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150409 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9659933 11321 Snai2 snail family zinc finger 2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 11321 Snai2 snail family zinc finger 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 11321 Snai2 snail family zinc finger 2 gene MP:0001310 abnormal conjunctiva morphology IAGP N RGD:5509061 20141003 MGI PMID:9659933 11321 Snai2 snail family zinc finger 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:12444107 11321 Snai2 snail family zinc finger 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12444107 11321 Snai2 snail family zinc finger 2 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:12398892 11321 Snai2 snail family zinc finger 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12398892 11321 Snai2 snail family zinc finger 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9659933 11321 Snai2 snail family zinc finger 2 gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20150409 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:9659933 11321 Snai2 snail family zinc finger 2 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 11321 Snai2 snail family zinc finger 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20150409 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20230601 MGI 11321 Snai2 snail family zinc finger 2 gene MP:0002083 premature death IAGP N RGD:5509061 20150409 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20150409 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20150409 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20150409 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12398892 11321 Snai2 snail family zinc finger 2 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:12444107 11321 Snai2 snail family zinc finger 2 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 11321 Snai2 snail family zinc finger 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12149208 11321 Snai2 snail family zinc finger 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16801545 11321 Snai2 snail family zinc finger 2 gene MP:0004378 frontal bone foramen IAGP N RGD:5509061 20141003 MGI PMID:17376812 11321 Snai2 snail family zinc finger 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20150409 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20150409 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:12398892 11321 Snai2 snail family zinc finger 2 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:9659933 11321 Snai2 snail family zinc finger 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20150409 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17376812 11321 Snai2 snail family zinc finger 2 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20150903 MGI PMID:18663143 11321 Snai2 snail family zinc finger 2 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20150409 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20150903 MGI PMID:18663143 11321 Snai2 snail family zinc finger 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:17376812 11321 Snai2 snail family zinc finger 2 gene MP:0009889 persistence of medial edge epithelium during palatal shelf fusion IAGP N RGD:5509061 20141003 MGI PMID:17376812 11321 Snai2 snail family zinc finger 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:17376812 11321 Snai2 snail family zinc finger 2 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20150409 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17376812 11321 Snai2 snail family zinc finger 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20150416 MGI PMID:17376812 11321 Snai2 snail family zinc finger 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 11321 Snai2 snail family zinc finger 2 gene MP:0014129 thymus fibrosis IAGP N RGD:5509061 20160324 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0014350 disorganized spleen B cell follicle IAGP N RGD:5509061 20240104 MGI PMID:23874916 11321 Snai2 snail family zinc finger 2 gene MP:0030054 decreased forehead pigmentation IAGP N RGD:5509061 20170921 MGI PMID:12444107 11321 Snai2 snail family zinc finger 2 gene MP:0030280 short parietal bone IAGP N RGD:5509061 20171207 MGI PMID:17376812 11321 Snai2 snail family zinc finger 2 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:17376812 11323 Tagln transgelin gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21693521 11323 Tagln transgelin gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17901360 11323 Tagln transgelin gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17901360 11323 Tagln transgelin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17901360 11323 Tagln transgelin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18311138 11323 Tagln transgelin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11158319 11323 Tagln transgelin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16484601 11323 Tagln transgelin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20428474 11323 Tagln transgelin gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21693521 11323 Tagln transgelin gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:20080989 11323 Tagln transgelin gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:18311138 11323 Tagln transgelin gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0003622 ischuria IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21693521 11323 Tagln transgelin gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:24016759 11323 Tagln transgelin gene MP:0004181 abnormal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21693521 11323 Tagln transgelin gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20160804 MGI PMID:25872946 11323 Tagln transgelin gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:24016759 11323 Tagln transgelin gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0008802 abnormal intestinal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0009485 distended ileum IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18311138 11323 Tagln transgelin gene MP:0010352 gastrointestinal tract polyps IAGP N RGD:5509061 20141003 MGI PMID:18311138 11323 Tagln transgelin gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0010478 intracranial aneurysm IAGP N RGD:5509061 20141003 MGI PMID:21693521 11323 Tagln transgelin gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:24016759 11323 Tagln transgelin gene MP:0011082 abnormal gastrointestinal motility IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0011503 distended jejunum IAGP N RGD:5509061 20141003 MGI PMID:18586037 11323 Tagln transgelin gene MP:0011513 abnormal vertebral artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21693521 11323 Tagln transgelin gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:18586037 11327892 Trbv19 T cell receptor beta, variable 19 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 11329 Sod1 superoxide dismutase 1, soluble gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:10464373 11329 Sod1 superoxide dismutase 1, soluble gene MP:0000160 kyphosis IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0000745 tremors IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:23729587 11329 Sod1 superoxide dismutase 1, soluble gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:23729587 11329 Sod1 superoxide dismutase 1, soluble gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:9724058 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:9724058 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:9724058 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:10679476 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001749 suppressed circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:9724058 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001860 liver inflammation IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9516486 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9724058 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9724058 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9516486 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9724058 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:16055286 11329 Sod1 superoxide dismutase 1, soluble gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0002083 premature death IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:23729587 11329 Sod1 superoxide dismutase 1, soluble gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:9724058 11329 Sod1 superoxide dismutase 1, soluble gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:9724058 11329 Sod1 superoxide dismutase 1, soluble gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:9724058 11329 Sod1 superoxide dismutase 1, soluble gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:10464373 11329 Sod1 superoxide dismutase 1, soluble gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:16055286 11329 Sod1 superoxide dismutase 1, soluble gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:10679476 11329 Sod1 superoxide dismutase 1, soluble gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0003354 astrocytosis IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:10679476 11329 Sod1 superoxide dismutase 1, soluble gene MP:0003674 oxidative stress IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10466888 11329 Sod1 superoxide dismutase 1, soluble gene MP:0004364 thin stria vascularis IAGP N RGD:5509061 20141003 MGI PMID:16055286 11329 Sod1 superoxide dismutase 1, soluble gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10464373 11329 Sod1 superoxide dismutase 1, soluble gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10466888 11329 Sod1 superoxide dismutase 1, soluble gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10464373 11329 Sod1 superoxide dismutase 1, soluble gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10466888 11329 Sod1 superoxide dismutase 1, soluble gene MP:0004586 pillar cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10466888 11329 Sod1 superoxide dismutase 1, soluble gene MP:0004597 increased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20141003 MGI PMID:10436316 11329 Sod1 superoxide dismutase 1, soluble gene MP:0004716 abnormal cochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10464373 11329 Sod1 superoxide dismutase 1, soluble gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:10464373 11329 Sod1 superoxide dismutase 1, soluble gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:23729587 11329 Sod1 superoxide dismutase 1, soluble gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10679476 11329 Sod1 superoxide dismutase 1, soluble gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21421868 11329 Sod1 superoxide dismutase 1, soluble gene MP:0005251 blepharitis IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0005252 abnormal Meibomian gland morphology IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:10679476 11329 Sod1 superoxide dismutase 1, soluble gene MP:0005356 positive geotaxis IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21421868 11329 Sod1 superoxide dismutase 1, soluble gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:10679476 11329 Sod1 superoxide dismutase 1, soluble gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:12485820 11329 Sod1 superoxide dismutase 1, soluble gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21421868 11329 Sod1 superoxide dismutase 1, soluble gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:21421868 11329 Sod1 superoxide dismutase 1, soluble gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200109 MGI PMID:18372426 11329 Sod1 superoxide dismutase 1, soluble gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20200109 MGI PMID:18372426 11329 Sod1 superoxide dismutase 1, soluble gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200109 MGI PMID:18372426 11329 Sod1 superoxide dismutase 1, soluble gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20200109 MGI PMID:18372426 11329 Sod1 superoxide dismutase 1, soluble gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0008918 microgliosis IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:23729587 11329 Sod1 superoxide dismutase 1, soluble gene MP:0009421 increased gastrocnemius weight IAGP N RGD:5509061 20141003 MGI PMID:23729587 11329 Sod1 superoxide dismutase 1, soluble gene MP:0009423 increased extensor digitorum longus weight IAGP N RGD:5509061 20141003 MGI PMID:23729587 11329 Sod1 superoxide dismutase 1, soluble gene MP:0009425 increased soleus weight IAGP N RGD:5509061 20141003 MGI PMID:23729587 11329 Sod1 superoxide dismutase 1, soluble gene MP:0009427 increased tibialis anterior weight IAGP N RGD:5509061 20141003 MGI PMID:23729587 11329 Sod1 superoxide dismutase 1, soluble gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9516486 11329 Sod1 superoxide dismutase 1, soluble gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9516486 11329 Sod1 superoxide dismutase 1, soluble gene MP:0009935 abnormal Meibomian gland acinus morphology IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11493445 11329 Sod1 superoxide dismutase 1, soluble gene MP:0010226 increased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:23729587 11329 Sod1 superoxide dismutase 1, soluble gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20150212 MGI PMID:9264557 11329 Sod1 superoxide dismutase 1, soluble gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:10464373 11329 Sod1 superoxide dismutase 1, soluble gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:10436316 11329 Sod1 superoxide dismutase 1, soluble gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:10464373 11329 Sod1 superoxide dismutase 1, soluble gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16055286 11329 Sod1 superoxide dismutase 1, soluble gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200109 MGI PMID:18372426 11329 Sod1 superoxide dismutase 1, soluble gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200109 MGI PMID:18372426 11329 Sod1 superoxide dismutase 1, soluble gene MP:0012320 abnormal body fat mass IAGP N RGD:5509061 20160304 MGI PMID:25468678 11329 Sod1 superoxide dismutase 1, soluble gene MP:0013391 abnormal Meibomian gland physiology IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0013392 Meibomian gland inflammation IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:9264557 11329 Sod1 superoxide dismutase 1, soluble gene MP:0020218 abnormal tear production IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0020220 decreased tear production IAGP N RGD:5509061 20150416 MGI PMID:25036096 11329 Sod1 superoxide dismutase 1, soluble gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:11493445 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15890620 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9462746 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19776389 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9462746 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000798 abnormal frontal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:9462746 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000906 abnormal trigeminal V mesencephalic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000911 abnormal trigeminal motor nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10762155 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:10762155 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001212 skin lesions IAGP N RGD:5509061 20161103 MGI PMID:26240345 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001218 thin epidermis IAGP N RGD:5509061 20161103 MGI PMID:26240345 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001219 thick epidermis IAGP N RGD:5509061 20161103 MGI PMID:26240345 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20161103 MGI PMID:26240345 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21571061 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19293248 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11527927 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200109 MGI PMID:26427390 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11527927 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9462746 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19293248 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10762155 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9462746 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:9462746 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:19293248 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15890620 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9462746 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:23862693 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14679299 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10762155 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19776389 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002319 hyperoxia IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002329 abnormal blood gas level IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:9462746 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:9462746 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20161103 MGI PMID:26240345 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20161103 MGI PMID:26240345 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20170914 MGI PMID:21195081 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:9462746 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170914 MGI PMID:21195081 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002833 increased heart weight IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002833 increased heart weight IAGP N RGD:5509061 20170914 MGI PMID:21195081 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002899 fatigue IAGP N RGD:5509061 20141003 MGI PMID:15890620 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002899 fatigue IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002899 fatigue IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002899 fatigue IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20161103 MGI PMID:26240345 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003027 abnormal blood pH regulation IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003031 acidosis IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003032 hypocapnia IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20141003 MGI PMID:19776389 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:19776389 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19293248 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20141003 MGI PMID:23862693 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003195 calcinosis IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15890620 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19293248 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:19776389 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:11226230 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:11514315 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:14679299 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:15890620 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:19293248 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:21571061 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003674 oxidative stress IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003674 oxidative stress IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003674 oxidative stress IAGP N RGD:5509061 20170914 MGI PMID:21195081 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11527927 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11226230 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19293248 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:19293248 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20170914 MGI PMID:21195081 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0004937 dilated heart IAGP N RGD:5509061 20170914 MGI PMID:21195081 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005098 abnormal optic choroid morphology IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005113 decreased spinal cord ventral horn cell number IAGP N RGD:5509061 20141003 MGI PMID:10762155 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11527927 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:9462746 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:19776389 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20200109 MGI PMID:26427390 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:19776389 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20170914 MGI PMID:21195081 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20170914 MGI PMID:21195081 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19776389 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9927656 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:11226230 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:11514315 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:19776389 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:19293248 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0006185 retina hemorrhage IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20161103 MGI PMID:26240345 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:9462746 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:11527927 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200109 MGI PMID:26427390 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20160616 MGI PMID:24985474 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19293248 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:10762155 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0009051 dilated distal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:21571061 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20161103 MGI PMID:26240345 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21571061 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:23862693 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:11226230 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:11514315 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20161103 MGI PMID:26240345 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:9927656 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20141003 MGI PMID:15721992 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20141003 MGI PMID:9927656 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011015 decreased body surface temperature IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15890620 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16497723 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19293248 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8790408 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9462746 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12176043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:21571061 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011687 decreased epidermal stem cell number IAGP N RGD:5509061 20161103 MGI PMID:26240345 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20170914 MGI PMID:21195081 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0011940 decreased food intake IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:19776389 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200109 MGI PMID:26427390 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200109 MGI PMID:26427390 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14679299 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20170921 MGI PMID:11677043 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20170921 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0012556 increased cell death IAGP N RGD:5509061 20141003 MGI PMID:23862693 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:7493016 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20170914 MGI PMID:16959785 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0014344 abnormal skeletal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:19776389 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0020543 decreased substantia nigra size IAGP N RGD:5509061 20180301 MGI PMID:10762155 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:19776389 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0030612 organic aciduria IAGP N RGD:5509061 20180906 MGI PMID:9927656 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:21195081 11330 Sod2 superoxide dismutase 2, mitochondrial gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:19293248 11331 Sod3 superoxide dismutase 3, extracellular gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20200402 MGI PMID:25085920 11331 Sod3 superoxide dismutase 3, extracellular gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20200402 MGI PMID:25085920 11331 Sod3 superoxide dismutase 3, extracellular gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18787098 11331 Sod3 superoxide dismutase 3, extracellular gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:15529385 11331 Sod3 superoxide dismutase 3, extracellular gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:15529385 11331 Sod3 superoxide dismutase 3, extracellular gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20200402 MGI PMID:25085920 11331 Sod3 superoxide dismutase 3, extracellular gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:7603981 11331 Sod3 superoxide dismutase 3, extracellular gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15529385 11331 Sod3 superoxide dismutase 3, extracellular gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20200402 MGI PMID:25085920 11331 Sod3 superoxide dismutase 3, extracellular gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:7603981 11331 Sod3 superoxide dismutase 3, extracellular gene MP:0010758 increased right ventricle systolic pressure IAGP N RGD:5509061 20200402 MGI PMID:25085920 11332 Sord sorbitol dehydrogenase gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:18760274 11332 Sord sorbitol dehydrogenase gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:18760274 11332 Sord sorbitol dehydrogenase gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:7708723 11332 Sord sorbitol dehydrogenase gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7708723 11332 Sord sorbitol dehydrogenase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9403062 11332 Sord sorbitol dehydrogenase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20220804 MGI PMID:35687590 11332 Sord sorbitol dehydrogenase gene MP:0005331 insulin resistance IAGP N RGD:5509061 20220804 MGI PMID:35687590 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:14585968 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14585968 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:14585968 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:14585968 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14585968 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:14585968 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23505376 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:14585968 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:14585968 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:14585968 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:14585968 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14585968 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:14585968 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0008221 abnormal hippocampal commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0009463 abnormal pituitary infundibular stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:23505376 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0013337 abnormal adenohypophysis development IAGP N RGD:5509061 20141211 MGI PMID:23505376 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0013342 bifurcated Rathke's pouch IAGP N RGD:5509061 20141204 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:14981518 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0014198 absent pituitary infundibular stalk IAGP N RGD:5509061 20160526 MGI PMID:23505376 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:14585968 11333 Sox3 SRY (sex determining region Y)-box 3 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:14981518 11334 Sp1 trans-acting transcription factor 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9160753 11334 Sp1 trans-acting transcription factor 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9160753 11334 Sp1 trans-acting transcription factor 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0010128 hypovolemia IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9160753 11334 Sp1 trans-acting transcription factor 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0011525 abnormal placenta intervillous maternal lacunae morphology IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0011527 disorganized placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0012109 decreased trophoblast glycogen cell number IAGP N RGD:5509061 20141003 MGI PMID:17584888 11334 Sp1 trans-acting transcription factor 1 gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20191219 MGI PMID:17584888 11335 Sp4 trans-acting transcription factor 4 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16430881 11335 Sp4 trans-acting transcription factor 4 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11532028 11335 Sp4 trans-acting transcription factor 4 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15558077 11335 Sp4 trans-acting transcription factor 4 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:15558077 11335 Sp4 trans-acting transcription factor 4 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11532028 11335 Sp4 trans-acting transcription factor 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11007485 11335 Sp4 trans-acting transcription factor 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16430881 11335 Sp4 trans-acting transcription factor 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8660867 11335 Sp4 trans-acting transcription factor 4 gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:8660867 11335 Sp4 trans-acting transcription factor 4 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:15558077 11335 Sp4 trans-acting transcription factor 4 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20634195 11335 Sp4 trans-acting transcription factor 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15558077 11335 Sp4 trans-acting transcription factor 4 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:15558077 11335 Sp4 trans-acting transcription factor 4 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:20634195 11335 Sp4 trans-acting transcription factor 4 gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15558077 11335 Sp4 trans-acting transcription factor 4 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:11007485 11335 Sp4 trans-acting transcription factor 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11532028 11335 Sp4 trans-acting transcription factor 4 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11532028 11335 Sp4 trans-acting transcription factor 4 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11532028 11335 Sp4 trans-acting transcription factor 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11532028 11335 Sp4 trans-acting transcription factor 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8660867 11335 Sp4 trans-acting transcription factor 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11007485 11335 Sp4 trans-acting transcription factor 4 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:15558077 11335 Sp4 trans-acting transcription factor 4 gene MP:0002635 reduced sensorimotor gating IAGP N RGD:5509061 20141003 MGI PMID:15558077 11335 Sp4 trans-acting transcription factor 4 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:11532028 11335 Sp4 trans-acting transcription factor 4 gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:11532028 11335 Sp4 trans-acting transcription factor 4 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:15558077 11335 Sp4 trans-acting transcription factor 4 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:11007485 11335 Sp4 trans-acting transcription factor 4 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:16430881 11335 Sp4 trans-acting transcription factor 4 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:15558077 11335 Sp4 trans-acting transcription factor 4 gene MP:0004085 abnormal heartbeat IAGP N RGD:5509061 20141003 MGI PMID:11007485 11335 Sp4 trans-acting transcription factor 4 gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:11007485 11335 Sp4 trans-acting transcription factor 4 gene MP:0004123 abnormal impulse conducting system morphology IAGP N RGD:5509061 20141003 MGI PMID:16430881 11335 Sp4 trans-acting transcription factor 4 gene MP:0004124 abnormal Purkinje fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11007485 11335 Sp4 trans-acting transcription factor 4 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:20634195 11335 Sp4 trans-acting transcription factor 4 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:8660867 11335 Sp4 trans-acting transcription factor 4 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:11007485 11335 Sp4 trans-acting transcription factor 4 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15558077 11335 Sp4 trans-acting transcription factor 4 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15558077 11335 Sp4 trans-acting transcription factor 4 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20141003 MGI PMID:11007485 11335 Sp4 trans-acting transcription factor 4 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:11007485 11335 Sp4 trans-acting transcription factor 4 gene MP:0010520 sinoatrial block IAGP N RGD:5509061 20141003 MGI PMID:11007485 11335 Sp4 trans-acting transcription factor 4 gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20141003 MGI PMID:11007485 11335 Sp4 trans-acting transcription factor 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11007485 11335 Sp4 trans-acting transcription factor 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11532028 11335 Sp4 trans-acting transcription factor 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8660867 11335 Sp4 trans-acting transcription factor 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16430881 11335 Sp4 trans-acting transcription factor 4 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20141003 MGI PMID:20634195 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:10749571 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10749571 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20160804 MGI 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0001258 decreased body length IEA N RGD:5509061 20160804 MGI 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:10079140 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:9856777 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0001304 cataract IEA N RGD:5509061 20141003 MGI 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:9856777 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9856777 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:10749571 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0001542 abnormal bone strength IAGP N RGD:5509061 20141003 MGI PMID:10749571 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:9856777 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20190124 MGI PMID:25340873 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20141003 MGI 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20141003 MGI 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:11748289 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0002834 decreased heart weight IEA N RGD:5509061 20160804 MGI 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10079140 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9856777 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:11532190 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:10749571 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0003099 retina detachment IAGP N RGD:5509061 20141003 MGI PMID:9856777 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0003236 abnormal lens capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:10079140 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0003236 abnormal lens capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:9856777 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10079140 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:12588887 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9524110 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:10749571 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:10749571 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:10749571 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:10749571 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20160804 MGI 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10749571 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0006201 vitreous body inflammation IAGP N RGD:5509061 20141003 MGI PMID:9856777 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20141003 MGI PMID:9856777 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0010096 abnormal incisor color IAGP N RGD:5509061 20190124 MGI PMID:25340873 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20141003 MGI 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0010251 subcapsular cataract IAGP N RGD:5509061 20141003 MGI PMID:9524110 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0010253 posterior subcapsular cataract IAGP N RGD:5509061 20141003 MGI PMID:10079140 11336 Sparc secreted acidic cysteine rich glycoprotein gene MP:0010255 cortical cataract IAGP N RGD:5509061 20141003 MGI PMID:9856777 11339 Spn sialophorin gene MP:0001257 increased body length IEA N RGD:5509061 20220519 MGI 11339 Spn sialophorin gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20200514 MGI 11339 Spn sialophorin gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 11339 Spn sialophorin gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11828253 11339 Spn sialophorin gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7566153 11339 Spn sialophorin gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 11339 Spn sialophorin gene MP:0004357 long tibia IEA N RGD:5509061 20211021 MGI 11339 Spn sialophorin gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:14662853 11339 Spn sialophorin gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201231 MGI 11339 Spn sialophorin gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7566153 11339 Spn sialophorin gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9645617 11339 Spn sialophorin gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 11339 Spn sialophorin gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20210128 MGI 11339 Spn sialophorin gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20211021 MGI 11340 Spp1 secreted phosphoprotein 1 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12073157 11340 Spp1 secreted phosphoprotein 1 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16939396 11340 Spp1 secreted phosphoprotein 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20170314 MGI PMID:18050311 11340 Spp1 secreted phosphoprotein 1 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17188882 11340 Spp1 secreted phosphoprotein 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18174176 11340 Spp1 secreted phosphoprotein 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14597759 11340 Spp1 secreted phosphoprotein 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19451692 11340 Spp1 secreted phosphoprotein 1 gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:12714436 11340 Spp1 secreted phosphoprotein 1 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:12714436 11340 Spp1 secreted phosphoprotein 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12391016 11340 Spp1 secreted phosphoprotein 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:15845900 11340 Spp1 secreted phosphoprotein 1 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19451692 11340 Spp1 secreted phosphoprotein 1 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:11375279 11340 Spp1 secreted phosphoprotein 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:15485631 11340 Spp1 secreted phosphoprotein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11737079 11340 Spp1 secreted phosphoprotein 1 gene MP:0000836 abnormal substantia nigra morphology IAGP N RGD:5509061 20141003 MGI PMID:17188882 11340 Spp1 secreted phosphoprotein 1 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:16105024 11340 Spp1 secreted phosphoprotein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16105024 11340 Spp1 secreted phosphoprotein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16939396 11340 Spp1 secreted phosphoprotein 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20201231 MGI 11340 Spp1 secreted phosphoprotein 1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:10393964 11340 Spp1 secreted phosphoprotein 1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:11278791 11340 Spp1 secreted phosphoprotein 1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20170314 MGI PMID:18050311 11340 Spp1 secreted phosphoprotein 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15165989 11340 Spp1 secreted phosphoprotein 1 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:18174176 11340 Spp1 secreted phosphoprotein 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12730087 11340 Spp1 secreted phosphoprotein 1 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:12714436 11340 Spp1 secreted phosphoprotein 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12714436 11340 Spp1 secreted phosphoprotein 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12391016 11340 Spp1 secreted phosphoprotein 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:11696588 11340 Spp1 secreted phosphoprotein 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:12466120 11340 Spp1 secreted phosphoprotein 1 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:10417195 11340 Spp1 secreted phosphoprotein 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:10657301 11340 Spp1 secreted phosphoprotein 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:11737079 11340 Spp1 secreted phosphoprotein 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16105024 11340 Spp1 secreted phosphoprotein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12391016 11340 Spp1 secreted phosphoprotein 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19451692 11340 Spp1 secreted phosphoprotein 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16105024 11340 Spp1 secreted phosphoprotein 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:415980 11340 Spp1 secreted phosphoprotein 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:415980 11340 Spp1 secreted phosphoprotein 1 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:15845900 11340 Spp1 secreted phosphoprotein 1 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:14597759 11340 Spp1 secreted phosphoprotein 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20170314 MGI PMID:18050311 11340 Spp1 secreted phosphoprotein 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:14597759 11340 Spp1 secreted phosphoprotein 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17823662 11340 Spp1 secreted phosphoprotein 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11737079 11340 Spp1 secreted phosphoprotein 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11737079 11340 Spp1 secreted phosphoprotein 1 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:10417195 11340 Spp1 secreted phosphoprotein 1 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:17003437 11340 Spp1 secreted phosphoprotein 1 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12714436 11340 Spp1 secreted phosphoprotein 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17823662 11340 Spp1 secreted phosphoprotein 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:10411681 11340 Spp1 secreted phosphoprotein 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17823662 11340 Spp1 secreted phosphoprotein 1 gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20160818 MGI PMID:22991301 11340 Spp1 secreted phosphoprotein 1 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:15165989 11340 Spp1 secreted phosphoprotein 1 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12714436 11340 Spp1 secreted phosphoprotein 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:18174176 11340 Spp1 secreted phosphoprotein 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:17823662 11340 Spp1 secreted phosphoprotein 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:12073157 11340 Spp1 secreted phosphoprotein 1 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:17898038 11340 Spp1 secreted phosphoprotein 1 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:17211411 11340 Spp1 secreted phosphoprotein 1 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:14597759 11340 Spp1 secreted phosphoprotein 1 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:17898038 11340 Spp1 secreted phosphoprotein 1 gene MP:0003279 aneurysm IAGP N RGD:5509061 20141003 MGI PMID:12391016 11340 Spp1 secreted phosphoprotein 1 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:11181551 11340 Spp1 secreted phosphoprotein 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12466120 11340 Spp1 secreted phosphoprotein 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:17823662 11340 Spp1 secreted phosphoprotein 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17823662 11340 Spp1 secreted phosphoprotein 1 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17898038 11340 Spp1 secreted phosphoprotein 1 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:17188882 11340 Spp1 secreted phosphoprotein 1 gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:10411681 11340 Spp1 secreted phosphoprotein 1 gene MP:0004262 abnormal physical strength IAGP N RGD:5509061 20141003 MGI PMID:19451692 11340 Spp1 secreted phosphoprotein 1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16849558 11340 Spp1 secreted phosphoprotein 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11737079 11340 Spp1 secreted phosphoprotein 1 gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11737079 11340 Spp1 secreted phosphoprotein 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:15845900 11340 Spp1 secreted phosphoprotein 1 gene MP:0004822 decreased susceptibility to experimental autoimmune uveoretinitis IAGP N RGD:5509061 20141003 MGI PMID:17003437 11340 Spp1 secreted phosphoprotein 1 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:17898038 11340 Spp1 secreted phosphoprotein 1 gene MP:0004880 lung cyst IAGP N RGD:5509061 20141003 MGI PMID:14977630 11340 Spp1 secreted phosphoprotein 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:12714436 11340 Spp1 secreted phosphoprotein 1 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19451692 11340 Spp1 secreted phosphoprotein 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:10393964 11340 Spp1 secreted phosphoprotein 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:9661074 11340 Spp1 secreted phosphoprotein 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:11181551 11340 Spp1 secreted phosphoprotein 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20170314 MGI PMID:18050311 11340 Spp1 secreted phosphoprotein 1 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:11181551 11340 Spp1 secreted phosphoprotein 1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:16939396 11340 Spp1 secreted phosphoprotein 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12714436 11340 Spp1 secreted phosphoprotein 1 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19451692 11340 Spp1 secreted phosphoprotein 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19451692 11340 Spp1 secreted phosphoprotein 1 gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:9525990 11340 Spp1 secreted phosphoprotein 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:10657301 11340 Spp1 secreted phosphoprotein 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:11751194 11340 Spp1 secreted phosphoprotein 1 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:15485631 11340 Spp1 secreted phosphoprotein 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15165989 11340 Spp1 secreted phosphoprotein 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:10411681 11340 Spp1 secreted phosphoprotein 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12730087 11340 Spp1 secreted phosphoprotein 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17823662 11340 Spp1 secreted phosphoprotein 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:14597759 11340 Spp1 secreted phosphoprotein 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12730087 11340 Spp1 secreted phosphoprotein 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:14597759 11340 Spp1 secreted phosphoprotein 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:6417017 11340 Spp1 secreted phosphoprotein 1 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:17301681 11340 Spp1 secreted phosphoprotein 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:10411681 11340 Spp1 secreted phosphoprotein 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17823662 11340 Spp1 secreted phosphoprotein 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:10411681 11340 Spp1 secreted phosphoprotein 1 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10657301 11340 Spp1 secreted phosphoprotein 1 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:11375279 11340 Spp1 secreted phosphoprotein 1 gene MP:0006133 calcified artery IAGP N RGD:5509061 20141003 MGI PMID:12391016 11340 Spp1 secreted phosphoprotein 1 gene MP:0006133 calcified artery IAGP N RGD:5509061 20141003 MGI PMID:12730087 11340 Spp1 secreted phosphoprotein 1 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12714436 11340 Spp1 secreted phosphoprotein 1 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:17898038 11340 Spp1 secreted phosphoprotein 1 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11737079 11340 Spp1 secreted phosphoprotein 1 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:11696588 11340 Spp1 secreted phosphoprotein 1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11737079 11340 Spp1 secreted phosphoprotein 1 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:11737079 11340 Spp1 secreted phosphoprotein 1 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:11737079 11340 Spp1 secreted phosphoprotein 1 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11737079 11340 Spp1 secreted phosphoprotein 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15485631 11340 Spp1 secreted phosphoprotein 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10657301 11340 Spp1 secreted phosphoprotein 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15485631 11340 Spp1 secreted phosphoprotein 1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:17823662 11340 Spp1 secreted phosphoprotein 1 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:10657301 11340 Spp1 secreted phosphoprotein 1 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:10657301 11340 Spp1 secreted phosphoprotein 1 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:10657301 11340 Spp1 secreted phosphoprotein 1 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:17823662 11340 Spp1 secreted phosphoprotein 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:14977630 11340 Spp1 secreted phosphoprotein 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11696588 11340 Spp1 secreted phosphoprotein 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15485631 11340 Spp1 secreted phosphoprotein 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17188882 11340 Spp1 secreted phosphoprotein 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:15165989 11340 Spp1 secreted phosphoprotein 1 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:17188882 11340 Spp1 secreted phosphoprotein 1 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:16939396 11340 Spp1 secreted phosphoprotein 1 gene MP:0009645 crystalluria IAGP N RGD:5509061 20141003 MGI PMID:12506146 11340 Spp1 secreted phosphoprotein 1 gene MP:0009645 crystalluria IAGP N RGD:5509061 20141003 MGI PMID:17898038 11340 Spp1 secreted phosphoprotein 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15845900 11340 Spp1 secreted phosphoprotein 1 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:6417017 11340 Spp1 secreted phosphoprotein 1 gene MP:0009810 increased urine uric acid level IAGP N RGD:5509061 20141003 MGI PMID:17898038 11340 Spp1 secreted phosphoprotein 1 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:17823662 11340 Spp1 secreted phosphoprotein 1 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10417195 11340 Spp1 secreted phosphoprotein 1 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20220922 MGI PMID:16939396 11340 Spp1 secreted phosphoprotein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16939396 11340 Spp1 secreted phosphoprotein 1 gene MP:0011165 abnormal tooth root development IAGP N RGD:5509061 20160818 MGI PMID:22991301 11340 Spp1 secreted phosphoprotein 1 gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17188882 11340 Spp1 secreted phosphoprotein 1 gene MP:0011460 decreased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:17898038 11340 Spp1 secreted phosphoprotein 1 gene MP:0011477 abnormal urine nucleoside level IAGP N RGD:5509061 20141003 MGI PMID:16105024 11340 Spp1 secreted phosphoprotein 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20220922 MGI PMID:16939396 11340 Spp1 secreted phosphoprotein 1 gene MP:0020416 decreased fibroblast chemotaxis IAGP N RGD:5509061 20170223 MGI PMID:10825241 11340 Spp1 secreted phosphoprotein 1 gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:10657301 11340 Spp1 secreted phosphoprotein 1 gene MP:0021189 increased bone mineral density of presacral vertebrae IAGP N RGD:5509061 20220922 MGI PMID:16939396 11340 Spp1 secreted phosphoprotein 1 gene MP:0021191 increased bone mineral density of lumbar vertebrae IAGP N RGD:5509061 20220922 MGI PMID:16939396 11340 Spp1 secreted phosphoprotein 1 gene MP:0031273 decreased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:14597759 11340 Spp1 secreted phosphoprotein 1 gene MP:0031518 calcified aortic valve cusp IAGP N RGD:5509061 20240118 MGI PMID:12466120 11340121 Trdc T cell receptor delta, constant region gene MP:0000706 small thymus IAGP N RGD:5509061 20160630 MGI PMID:22770884 11340121 Trdc T cell receptor delta, constant region gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160630 MGI PMID:16878135 11340121 Trdc T cell receptor delta, constant region gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20160630 MGI PMID:16878135 11340121 Trdc T cell receptor delta, constant region gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20160630 MGI PMID:22770884 11340121 Trdc T cell receptor delta, constant region gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20160630 MGI PMID:22770884 11340121 Trdc T cell receptor delta, constant region gene MP:0008348 absent gamma-delta T cells IAGP N RGD:5509061 20160630 MGI PMID:22770884 11341 Srd5a1 steroid 5 alpha-reductase 1 gene MP:0000664 small prostate gland anterior lobe IAGP N RGD:5509061 20141003 MGI PMID:11606430 11341 Srd5a1 steroid 5 alpha-reductase 1 gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:11606430 11341 Srd5a1 steroid 5 alpha-reductase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11606430 11341 Srd5a1 steroid 5 alpha-reductase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8721983 11341 Srd5a1 steroid 5 alpha-reductase 1 gene MP:0002774 small prostate gland IAGP N RGD:5509061 20141003 MGI PMID:11606430 11341 Srd5a1 steroid 5 alpha-reductase 1 gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20141003 MGI PMID:11606430 11341 Srd5a1 steroid 5 alpha-reductase 1 gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20141003 MGI PMID:8721983 11350 Star steroidogenic acute regulatory protein gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:10976923 11350 Star steroidogenic acute regulatory protein gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:10976923 11350 Star steroidogenic acute regulatory protein gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:10976923 11350 Star steroidogenic acute regulatory protein gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:10976923 11350 Star steroidogenic acute regulatory protein gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:10976923 11350 Star steroidogenic acute regulatory protein gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10976923 11350 Star steroidogenic acute regulatory protein gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:10976923 11350 Star steroidogenic acute regulatory protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0001754 increased circulating corticotropin-releasing hormone level IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0002774 small prostate gland IAGP N RGD:5509061 20141003 MGI PMID:10976923 11350 Star steroidogenic acute regulatory protein gene MP:0002774 small prostate gland IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10976923 11350 Star steroidogenic acute regulatory protein gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:10976923 11350 Star steroidogenic acute regulatory protein gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0004832 enlarged ovary IAGP N RGD:5509061 20141003 MGI PMID:10976923 11350 Star steroidogenic acute regulatory protein gene MP:0005129 increased adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0005147 prostate gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0005148 seminal vesicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0008299 adrenal cortical hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9326645 11350 Star steroidogenic acute regulatory protein gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9326645 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18552213 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19779039 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22520852 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9630227 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19779039 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9630227 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19779039 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19779039 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:15947484 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19779039 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15947484 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:9630227 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:9009201 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:15340066 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:9009201 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:9630227 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16493008 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10908145 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17158201 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:17599554 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:18286195 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17158201 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17504935 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9630227 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:18286195 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17158201 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18286195 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17599554 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18286195 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19779039 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9630227 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001881 abnormal mammary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:9630227 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9630227 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18286195 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16493008 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15340066 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22520852 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20180426 MGI PMID:28930659 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002415 abnormal neutrophil differentiation IAGP N RGD:5509061 20141003 MGI PMID:19779039 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:18552213 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12714518 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:19779039 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:16493008 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:18552213 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:18552213 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:18552213 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:9630227 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:18552213 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19779039 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:22520852 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18552213 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19779039 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22520852 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17599554 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:10908145 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0003838 abnormal milk ejection IAGP N RGD:5509061 20141003 MGI PMID:15340066 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:16493008 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:22520852 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:18286195 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17158201 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:17158201 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22520852 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19779039 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9630227 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:9841920 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22520852 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:18286195 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17158201 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17599554 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18286195 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:18286195 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18286195 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:9630227 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18286195 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19779039 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005462 abnormal mast cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12714518 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005462 abnormal mast cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15947484 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17599554 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:18552213 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17599554 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18286195 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18552213 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19779039 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:9009201 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:19833766 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:9009201 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22520852 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:22520852 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:9841920 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23727894 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16493008 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22520852 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22520852 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:18552213 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:17363300 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:17363300 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:18552213 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:18552213 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18286195 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18552213 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20200402 MGI PMID:31806625 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:17599554 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:9841920 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:15340066 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:19833766 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0009737 prostate gland cyst IAGP N RGD:5509061 20141003 MGI PMID:10908145 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17158201 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17599554 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18286195 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:18552213 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20200402 MGI PMID:31806625 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16493008 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0010172 abnormal mammary gland epithelium physiology IAGP N RGD:5509061 20160317 MGI PMID:15340066 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:19833766 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:9009201 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:18286195 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0011696 absent mast cells IAGP N RGD:5509061 20141003 MGI PMID:12714518 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20200402 MGI PMID:31806625 11351 Stat5a signal transducer and activator of transcription 5A gene MP:0014126 increased mammary gland apoptosis IAGP N RGD:5509061 20160317 MGI PMID:15340066 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18552213 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19779039 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22520852 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9630227 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19779039 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9630227 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19779039 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19779039 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19779039 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:9207075 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:9207075 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:9207075 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:9207075 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:9630227 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:9207075 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:15340066 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16493008 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:9841920 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9841920 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17158201 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:17599554 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:18286195 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:9207075 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17158201 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17504935 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9207075 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9630227 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:18286195 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17158201 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18286195 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17599554 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18286195 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19779039 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9630227 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001881 abnormal mammary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:9630227 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9630227 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:9207075 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18286195 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16493008 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15340066 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22520852 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20180426 MGI PMID:28930659 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9841920 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002415 abnormal neutrophil differentiation IAGP N RGD:5509061 20141003 MGI PMID:19779039 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:18552213 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12714518 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:19779039 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:16493008 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9841920 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:18552213 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:18552213 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:18552213 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:9630227 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:18552213 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19779039 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:22520852 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18552213 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19779039 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22520852 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17599554 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0003838 abnormal milk ejection IAGP N RGD:5509061 20141003 MGI PMID:15340066 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:16493008 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:22520852 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:18286195 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17158201 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:17158201 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:9207075 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22520852 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19779039 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9630227 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:9841920 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22520852 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9841920 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:9207075 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:18286195 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17158201 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17599554 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18286195 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:18286195 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18286195 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:9630227 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18286195 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19779039 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005462 abnormal mast cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12714518 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17599554 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:18552213 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17599554 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18286195 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18552213 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19779039 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:19833766 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22520852 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:22520852 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:9841920 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23727894 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16493008 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22520852 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9841920 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22520852 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:18552213 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:17363300 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:17363300 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:18552213 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:18552213 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18286195 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18552213 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:17599554 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:9841920 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:15340066 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:19833766 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17158201 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17599554 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18286195 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:9207075 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:18552213 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16493008 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0010172 abnormal mammary gland epithelium physiology IAGP N RGD:5509061 20160317 MGI PMID:15340066 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:19833766 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:18286195 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0011532 decreased urine major urinary protein level IAGP N RGD:5509061 20141003 MGI PMID:9207075 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0011696 absent mast cells IAGP N RGD:5509061 20141003 MGI PMID:12714518 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0013716 hypolactation IAGP N RGD:5509061 20150611 MGI PMID:9207075 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0014126 increased mammary gland apoptosis IAGP N RGD:5509061 20160317 MGI PMID:15340066 11352 Stat5b signal transducer and activator of transcription 5B gene MP:0031434 increased miscarriage rate IAGP N RGD:5509061 20220915 MGI PMID:9207075 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:11713234 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:11713234 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11713234 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15685171 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11713234 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15685171 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11713234 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:11713234 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11713234 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11713234 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0004909 increased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:11713234 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:11713234 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:15685171 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:15685171 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0012172 abnormal amniotic fluid composition IAGP N RGD:5509061 20141003 MGI PMID:15685171 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0013598 Leydig cell hypertrophy IAGP N RGD:5509061 20150319 MGI PMID:11713234 11353 Sult1e1 sulfotransferase family 1E, member 1 gene MP:0020407 abnormal placental thrombosis IAGP N RGD:5509061 20161124 MGI PMID:15685171 11354953 Mom21_m modifier of Min 21 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20160729 MGI Created by mouse qtl pipeline PMID:17435219 11354953 Mom21_m modifier of Min 21 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17435219 11354953 Mom21_m modifier of Min 21 (mouse) qtl MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20160804 MGI PMID:17435219 11361 Stxbp1 syntaxin binding protein 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 11361 Stxbp1 syntaxin binding protein 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:15255974 11361 Stxbp1 syntaxin binding protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15255974 11361 Stxbp1 syntaxin binding protein 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 11361 Stxbp1 syntaxin binding protein 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 11361 Stxbp1 syntaxin binding protein 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20220519 MGI 11361 Stxbp1 syntaxin binding protein 1 gene MP:0001785 edema IEA N RGD:5509061 20220519 MGI 11361 Stxbp1 syntaxin binding protein 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20220519 MGI 11361 Stxbp1 syntaxin binding protein 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:10657302 11361 Stxbp1 syntaxin binding protein 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 11361 Stxbp1 syntaxin binding protein 1 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20201022 MGI 11361 Stxbp1 syntaxin binding protein 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:15255974 11361 Stxbp1 syntaxin binding protein 1 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:10657302 11361 Stxbp1 syntaxin binding protein 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 11361 Stxbp1 syntaxin binding protein 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220811 MGI 11361 Stxbp1 syntaxin binding protein 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:12895513 11361 Stxbp1 syntaxin binding protein 1 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:10657302 11361 Stxbp1 syntaxin binding protein 1 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:15255974 11361 Stxbp1 syntaxin binding protein 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 11361 Stxbp1 syntaxin binding protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10657302 11361 Stxbp1 syntaxin binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11562480 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12122112 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:12122112 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20160602 MGI PMID:24648545 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20211202 MGI PMID:33529173 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20211202 MGI PMID:33529173 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0001596 hypotension IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11562480 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12122112 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0002083 premature death IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20200227 MGI PMID:31575858 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20160602 MGI PMID:24648545 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20200227 MGI PMID:31575858 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11562480 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20211202 MGI PMID:33529173 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20200227 MGI PMID:31575858 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20200227 MGI PMID:31575858 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20160602 MGI PMID:24648545 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0003897 abnormal ST segment IAGP N RGD:5509061 20141003 MGI PMID:12122112 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0004937 dilated heart IAGP N RGD:5509061 20211202 MGI PMID:33529173 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0005039 hypoxia IAGP N RGD:5509061 20160602 MGI PMID:24648545 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160602 MGI PMID:24648545 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20160602 MGI PMID:24648545 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11562480 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20160602 MGI PMID:24648545 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:12122112 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20160602 MGI PMID:24648545 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0006135 artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:12122112 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12122112 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12122112 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20160602 MGI PMID:24648545 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11562480 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20160602 MGI PMID:24648545 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20211202 MGI PMID:33529173 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20211202 MGI PMID:33529173 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0010468 abnormal thoracic aorta morphology IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0010574 dilated aorta IAGP N RGD:5509061 20211202 MGI PMID:33529173 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0010575 aortic arch dilation IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160602 MGI PMID:24648545 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20160602 MGI PMID:24648545 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20160602 MGI PMID:24648545 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20200227 MGI PMID:31575858 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20200220 MGI PMID:30089727 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20160602 MGI PMID:24648545 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:24648545 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0020345 abnormal myocardial fiber currents IAGP N RGD:5509061 20211202 MGI PMID:33529173 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0031192 coronary artery spasm IAGP N RGD:5509061 20201119 MGI PMID:12122112 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:11562480 11362 Abcc9 ATP-binding cassette, sub-family C member 9 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:31575858 11367 Sycp1 synaptonemal complex protein 1 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15937223 11367 Sycp1 synaptonemal complex protein 1 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15937223 11367 Sycp1 synaptonemal complex protein 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:15937223 11367 Sycp1 synaptonemal complex protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15937223 11367 Sycp1 synaptonemal complex protein 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15937223 11367 Sycp1 synaptonemal complex protein 1 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:15937223 11367 Sycp1 synaptonemal complex protein 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:15937223 11367 Sycp1 synaptonemal complex protein 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15937223 11367 Sycp1 synaptonemal complex protein 1 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:15937223 11367 Sycp1 synaptonemal complex protein 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:15937223 11367 Sycp1 synaptonemal complex protein 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:15937223 11367 Sycp1 synaptonemal complex protein 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:22761591 11367 Sycp1 synaptonemal complex protein 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:15937223 11368 Sycp3 synaptonemal complex protein 3 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:10678170 11368 Sycp3 synaptonemal complex protein 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12004129 11368 Sycp3 synaptonemal complex protein 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10678170 11368 Sycp3 synaptonemal complex protein 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12004129 11368 Sycp3 synaptonemal complex protein 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10678170 11368 Sycp3 synaptonemal complex protein 3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:10678170 11368 Sycp3 synaptonemal complex protein 3 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:12004129 11368 Sycp3 synaptonemal complex protein 3 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10678170 11368 Sycp3 synaptonemal complex protein 3 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:10678170 11368 Sycp3 synaptonemal complex protein 3 gene MP:0011954 shortened PQ interval IEA N RGD:5509061 20211021 MGI 11370 Syn1 synapsin I gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:7777057 11370 Syn1 synapsin I gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:7902212 11370 Syn1 synapsin I gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:23280234 11370 Syn1 synapsin I gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:23280234 11370 Syn1 synapsin I gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20141003 MGI PMID:7568108 11370 Syn1 synapsin I gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:23280234 11370 Syn1 synapsin I gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:7568108 11370 Syn1 synapsin I gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:7568108 11370 Syn1 synapsin I gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:7777057 11370 Syn1 synapsin I gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:7902212 11370 Syn1 synapsin I gene MP:0002922 decreased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:7777057 11370 Syn1 synapsin I gene MP:0002924 delayed CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:7568107 11370 Syn1 synapsin I gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:10352020 11370 Syn1 synapsin I gene MP:0002969 impaired social transmission of food preference IAGP N RGD:5509061 20141003 MGI PMID:23280234 11370 Syn1 synapsin I gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20151224 MGI PMID:21621590 11370 Syn1 synapsin I gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:10352020 11370 Syn1 synapsin I gene MP:0004793 abnormal synaptic vesicle clustering IAGP N RGD:5509061 20141003 MGI PMID:10352020 11370 Syn1 synapsin I gene MP:0004793 abnormal synaptic vesicle clustering IAGP N RGD:5509061 20141003 MGI PMID:7568108 11370 Syn1 synapsin I gene MP:0004793 abnormal synaptic vesicle clustering IAGP N RGD:5509061 20141003 MGI PMID:8557745 11370 Syn1 synapsin I gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20151224 MGI PMID:21621590 11370 Syn1 synapsin I gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:8557745 11370 Syn1 synapsin I gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:9513186 11370 Syn1 synapsin I gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:7568108 11370 Syn1 synapsin I gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20151224 MGI PMID:21621590 11370 Syn1 synapsin I gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7568107 11373 Syp synaptophysin gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10595519 11373 Syp synaptophysin gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:10595519 11373 Syp synaptophysin gene MP:0002064 seizures IEA N RGD:5509061 20150219 MGI 11373 Syp synaptophysin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8581936 11373 Syp synaptophysin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8643476 11373 Syp synaptophysin gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230601 MGI 11373 Syp synaptophysin gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:10595519 11373 Syp synaptophysin gene MP:0002922 decreased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:10595519 11379 Tac1 tachykinin 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12427862 11379 Tac1 tachykinin 1 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:11433347 11379 Tac1 tachykinin 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20240314 MGI 11379 Tac1 tachykinin 1 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:9482938 11379 Tac1 tachykinin 1 gene MP:0003063 increased coping response IAGP N RGD:5509061 20141003 MGI PMID:12427862 11379 Tac1 tachykinin 1 gene MP:0003280 urinary incontinence IAGP N RGD:5509061 20141003 MGI PMID:11684339 11379 Tac1 tachykinin 1 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:11684339 11380 Tacr3 tachykinin receptor 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220811 MGI 11380 Tacr3 tachykinin receptor 3 gene MP:0001147 small testis IAGP N RGD:5509061 20160421 MGI PMID:22253416 11380 Tacr3 tachykinin receptor 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17558564 11380 Tacr3 tachykinin receptor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160421 MGI PMID:22253416 11380 Tacr3 tachykinin receptor 3 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210826 MGI 11380 Tacr3 tachykinin receptor 3 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17558564 11380 Tacr3 tachykinin receptor 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20160421 MGI PMID:22253416 11380 Tacr3 tachykinin receptor 3 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 11380 Tacr3 tachykinin receptor 3 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20160421 MGI PMID:22253416 11380 Tacr3 tachykinin receptor 3 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20160421 MGI PMID:22253416 11380 Tacr3 tachykinin receptor 3 gene MP:0002798 abnormal active avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:17558564 11380 Tacr3 tachykinin receptor 3 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:17558564 11380 Tacr3 tachykinin receptor 3 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20160421 MGI PMID:22253416 11380 Tacr3 tachykinin receptor 3 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20160421 MGI PMID:22253416 11380 Tacr3 tachykinin receptor 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 11380 Tacr3 tachykinin receptor 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210520 MGI 11380 Tacr3 tachykinin receptor 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:1473153 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:11118151 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001606 impaired hematopoiesis IEA N RGD:5509061 20161201 MGI 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:16505142 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001836 abnormal antigen presentation via MHC class I IAGP N RGD:5509061 20141003 MGI PMID:10973281 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001836 abnormal antigen presentation via MHC class I IAGP N RGD:5509061 20141003 MGI PMID:16299505 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001836 abnormal antigen presentation via MHC class I IAGP N RGD:5509061 20141003 MGI PMID:17128277 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001837 defective assembly of class I molecules IAGP N RGD:5509061 20141003 MGI PMID:10981964 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001838 defective intracellular transport of class I molecules IAGP N RGD:5509061 20141003 MGI PMID:10981964 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001838 defective intracellular transport of class I molecules IAGP N RGD:5509061 20141003 MGI PMID:1473153 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:10973281 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:10981964 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:1473153 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:11118151 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17562770 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23243279 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:10973281 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:9892619 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11118151 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16505142 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0004165 abnormal lateral geniculate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11118151 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17420446 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:17420446 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20171214 MGI PMID:21964024 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:10973281 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:1473153 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:12634786 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10973281 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10981964 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17562770 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19721454 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:17562770 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:11118151 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:17420446 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0009222 increased uterus tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:17420446 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17562770 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20180215 MGI 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0010839 decreased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20180215 MGI 11387 Tap1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0020916 increased susceptibility to Herpesvirales infection IEA N RGD:5509061 20200430 MGI 11388 Tap2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0000727 absent CD8-positive, alpha-beta T cells IEA N RGD:5509061 20111116 MGI 11388 Tap2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001837 defective assembly of class I molecules IEA N RGD:5509061 20111116 MGI 11388 Tap2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0001841 decreased level of surface class I molecules IEA N RGD:5509061 20111116 MGI 11388 Tap2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0005078 abnormal cytotoxic T cell physiology IEA N RGD:5509061 20111116 MGI 11388 Tap2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20180215 MGI 11388 Tap2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20150205 MGI 11388 Tap2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19721454 11388 Tap2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0010766 abnormal NK cell physiology IEA N RGD:5509061 20111116 MGI 11388 Tap2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0010845 decreased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 11388 Tap2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 11388 Tap2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 11391 Tat tyrosine aminotransferase gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210128 MGI 11391 Tat tyrosine aminotransferase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210128 MGI 11391 Tat tyrosine aminotransferase gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 11391 Tat tyrosine aminotransferase gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 11391 Tat tyrosine aminotransferase gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 11391 Tat tyrosine aminotransferase gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220519 MGI 11391 Tat tyrosine aminotransferase gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210128 MGI 11391 Tat tyrosine aminotransferase gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 11391 Tat tyrosine aminotransferase gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220519 MGI 11391 Tat tyrosine aminotransferase gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 11391 Tat tyrosine aminotransferase gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20210520 MGI 11391 Tat tyrosine aminotransferase gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210128 MGI 11391 Tat tyrosine aminotransferase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 11392 Cntn2 contactin 2 gene MP:0000576 clubfoot IAGP N RGD:5509061 20141003 MGI PMID:23968836 11392 Cntn2 contactin 2 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:23968836 11392 Cntn2 contactin 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:23968836 11392 Cntn2 contactin 2 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:11178983 11392 Cntn2 contactin 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:18550718 11392 Cntn2 contactin 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:11178983 11392 Cntn2 contactin 2 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:23968836 11392 Cntn2 contactin 2 gene MP:0004103 abnormal ventral striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:23968836 11392 Cntn2 contactin 2 gene MP:0005423 abnormal somatic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18550718 11392 Cntn2 contactin 2 gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:18550718 11392 Cntn2 contactin 2 gene MP:0008129 absent brain internal capsule IAGP N RGD:5509061 20141003 MGI PMID:23968836 11392 Cntn2 contactin 2 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:23968836 11392 Cntn2 contactin 2 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:23968836 11392 Cntn2 contactin 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:23968836 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0000274 enlarged heart IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20170314 MGI PMID:26114544 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0001147 small testis IAGP N RGD:5509061 20170314 MGI PMID:26114544 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0001925 male infertility IAGP N RGD:5509061 20170314 MGI PMID:26114544 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0002083 premature death IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20170314 MGI PMID:26114544 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0005159 azoospermia IAGP N RGD:5509061 20170314 MGI PMID:26114544 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20170314 MGI PMID:26114544 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20170314 MGI PMID:26114544 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20230907 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:34129362 11393 Tafazzin tafazzin, phospholipid-lysophospholipid transacylase gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:34129362 11394 Tbxas1 thromboxane A synthase 1, platelet gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15010374 11394 Tbxas1 thromboxane A synthase 1, platelet gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:15010374 11394 Tbxas1 thromboxane A synthase 1, platelet gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:15010374 11395 Eloa elongin A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 11395 Eloa elongin A gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 11395 Eloa elongin A gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:17170753 11395 Eloa elongin A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17170753 11395 Eloa elongin A gene MP:0000597 delayed hepatic development IAGP N RGD:5509061 20141003 MGI PMID:17170753 11395 Eloa elongin A gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 11395 Eloa elongin A gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 11395 Eloa elongin A gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 11395 Eloa elongin A gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 11395 Eloa elongin A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17170753 11395 Eloa elongin A gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20210826 MGI 11395 Eloa elongin A gene MP:0001889 delayed brain development IAGP N RGD:5509061 20141003 MGI PMID:17170753 11395 Eloa elongin A gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 11395 Eloa elongin A gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 11395 Eloa elongin A gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17170753 11395 Eloa elongin A gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17170753 11395 Eloa elongin A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17170753 11395 Eloa elongin A gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17170753 11395 Eloa elongin A gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:17170753 11395 Eloa elongin A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17170753 11395 Eloa elongin A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11395 Eloa elongin A gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:17170753 11395 Eloa elongin A gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17170753 11395 Eloa elongin A gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17170753 11397 Hnf1a HNF1 homeobox A gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12529398 11397 Hnf1a HNF1 homeobox A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:12529398 11397 Hnf1a HNF1 homeobox A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20181220 MGI PMID:9593777 11397 Hnf1a HNF1 homeobox A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12529398 11397 Hnf1a HNF1 homeobox A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12529398 11397 Hnf1a HNF1 homeobox A gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:12529398 11397 Hnf1a HNF1 homeobox A gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12529398 11397 Hnf1a HNF1 homeobox A gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12529398 11397 Hnf1a HNF1 homeobox A gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0002985 abnormal urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20181220 MGI PMID:9593777 11397 Hnf1a HNF1 homeobox A gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0003325 decreased liver function IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20181220 MGI PMID:9593777 11397 Hnf1a HNF1 homeobox A gene MP:0008822 decreased blood uric acid level IAGP N RGD:5509061 20240912 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0009109 decreased pancreas weight IAGP N RGD:5509061 20181220 MGI PMID:9593777 11397 Hnf1a HNF1 homeobox A gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20181220 MGI PMID:9593777 11397 Hnf1a HNF1 homeobox A gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20181220 MGI PMID:9593777 11397 Hnf1a HNF1 homeobox A gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0009810 increased urine uric acid level IAGP N RGD:5509061 20161208 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9566924 11397 Hnf1a HNF1 homeobox A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20161208 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0011447 abnormal renal glucose reabsorption IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0011765 oroticaciduria IAGP N RGD:5509061 20141003 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0020401 argininuria IAGP N RGD:5509061 20161208 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0030662 decreased circulating arginine level IAGP N RGD:5509061 20240912 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0030670 increased circulating phenylalanine level IAGP N RGD:5509061 20240912 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0030681 increased circulating hydroxyproline level IAGP N RGD:5509061 20240912 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0030682 hydroxyprolinuria IAGP N RGD:5509061 20240912 MGI PMID:8598044 11397 Hnf1a HNF1 homeobox A gene MP:0030719 decreased circulating lysine level IAGP N RGD:5509061 20240912 MGI PMID:8598044 11398 Hnf1b HNF1 homeobox B gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:23362348 11398 Hnf1b HNF1 homeobox B gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20210701 MGI PMID:33527355 11398 Hnf1b HNF1 homeobox B gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:10518496 11398 Hnf1b HNF1 homeobox B gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:10518495 11398 Hnf1b HNF1 homeobox B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10518495 11398 Hnf1b HNF1 homeobox B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10518496 11398 Hnf1b HNF1 homeobox B gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:10518495 11398 Hnf1b HNF1 homeobox B gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10518495 11398 Hnf1b HNF1 homeobox B gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10518496 11398 Hnf1b HNF1 homeobox B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:10518496 11398 Hnf1b HNF1 homeobox B gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10518496 11398 Hnf1b HNF1 homeobox B gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10518496 11398 Hnf1b HNF1 homeobox B gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:23362348 11398 Hnf1b HNF1 homeobox B gene MP:0002138 abnormal hepatobiliary system morphology IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0002139 abnormal hepatobiliary system physiology IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:10518495 11398 Hnf1b HNF1 homeobox B gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:10518495 11398 Hnf1b HNF1 homeobox B gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23362348 11398 Hnf1b HNF1 homeobox B gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:10518496 11398 Hnf1b HNF1 homeobox B gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20210701 MGI PMID:33527355 11398 Hnf1b HNF1 homeobox B gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20210701 MGI PMID:33527355 11398 Hnf1b HNF1 homeobox B gene MP:0003252 abnormal bile duct physiology IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0003325 decreased liver function IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0003334 pancreas fibrosis IAGP N RGD:5509061 20210701 MGI PMID:33527355 11398 Hnf1b HNF1 homeobox B gene MP:0003338 pancreas lipomatosis IAGP N RGD:5509061 20210701 MGI PMID:33527355 11398 Hnf1b HNF1 homeobox B gene MP:0003341 chronic pancreas inflammation IAGP N RGD:5509061 20210701 MGI PMID:33527355 11398 Hnf1b HNF1 homeobox B gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:10518496 11398 Hnf1b HNF1 homeobox B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10518496 11398 Hnf1b HNF1 homeobox B gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:10518495 11398 Hnf1b HNF1 homeobox B gene MP:0004755 abnormal loop of Henle morphology IAGP N RGD:5509061 20141003 MGI PMID:23362348 11398 Hnf1b HNF1 homeobox B gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23362348 11398 Hnf1b HNF1 homeobox B gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210701 MGI PMID:33527355 11398 Hnf1b HNF1 homeobox B gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0009143 abnormal pancreatic duct morphology IAGP N RGD:5509061 20210701 MGI PMID:33527355 11398 Hnf1b HNF1 homeobox B gene MP:0009149 decreased pancreatic acinar cell number IAGP N RGD:5509061 20210701 MGI PMID:33527355 11398 Hnf1b HNF1 homeobox B gene MP:0009154 pancreatic acinar hypoplasia IAGP N RGD:5509061 20210701 MGI PMID:33527355 11398 Hnf1b HNF1 homeobox B gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20210701 MGI PMID:33527355 11398 Hnf1b HNF1 homeobox B gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20210701 MGI PMID:33527355 11398 Hnf1b HNF1 homeobox B gene MP:0009492 abnormal gallbladder epithelium morphology IAGP N RGD:5509061 20200102 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0009493 abnormal cystic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0009497 abnormal intrahepatic bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0009498 abnormal extrahepatic bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0009500 abnormal interlobular bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:11934849 11398 Hnf1b HNF1 homeobox B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23362348 11398 Hnf1b HNF1 homeobox B gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10518495 11398 Hnf1b HNF1 homeobox B gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10518496 11398 Hnf1b HNF1 homeobox B gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10518496 11398 Hnf1b HNF1 homeobox B gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10518495 11398 Hnf1b HNF1 homeobox B gene MP:0011198 absent proamniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:10518496 11398 Hnf1b HNF1 homeobox B gene MP:0011207 absent ectoplacental cavity IAGP N RGD:5509061 20141003 MGI PMID:10518496 11398 Hnf1b HNF1 homeobox B gene MP:0011364 abnormal metanephros morphology IAGP N RGD:5509061 20141003 MGI PMID:23362348 11398 Hnf1b HNF1 homeobox B gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:23362348 11398 Hnf1b HNF1 homeobox B gene MP:0012158 absent visceral endoderm IAGP N RGD:5509061 20141003 MGI PMID:10518496 11398 Hnf1b HNF1 homeobox B gene MP:0012162 absent parietal endoderm IAGP N RGD:5509061 20141003 MGI PMID:10518496 11398 Hnf1b HNF1 homeobox B gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20210701 MGI PMID:33527355 11398 Hnf1b HNF1 homeobox B gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20210701 MGI PMID:33527355 11402 Tcrb T cell receptor beta chain gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:22341446 11402 Tcrb T cell receptor beta chain gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22341446 11402 Tcrb T cell receptor beta chain gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19017966 11402 Tcrb T cell receptor beta chain gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:1359428 11402 Tcrb T cell receptor beta chain gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:18997009 11402 Tcrb T cell receptor beta chain gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:16103410 11402 Tcrb T cell receptor beta chain gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16103410 11402 Tcrb T cell receptor beta chain gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15964276 11402 Tcrb T cell receptor beta chain gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18997009 11402 Tcrb T cell receptor beta chain gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11937563 11402 Tcrb T cell receptor beta chain gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16272283 11402 Tcrb T cell receptor beta chain gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15770700 11402 Tcrb T cell receptor beta chain gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:1359428 11402 Tcrb T cell receptor beta chain gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17617584 11402 Tcrb T cell receptor beta chain gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10850719 11402 Tcrb T cell receptor beta chain gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:1359428 11402 Tcrb T cell receptor beta chain gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22341446 11402 Tcrb T cell receptor beta chain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18997009 11402 Tcrb T cell receptor beta chain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22341446 11402 Tcrb T cell receptor beta chain gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:16272283 11402 Tcrb T cell receptor beta chain gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11937563 11402 Tcrb T cell receptor beta chain gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:16272283 11402 Tcrb T cell receptor beta chain gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9075933 11402 Tcrb T cell receptor beta chain gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17410206 11402 Tcrb T cell receptor beta chain gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17617584 11402 Tcrb T cell receptor beta chain gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12847251 11402 Tcrb T cell receptor beta chain gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17617584 11402 Tcrb T cell receptor beta chain gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19380806 11402 Tcrb T cell receptor beta chain gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11937563 11402 Tcrb T cell receptor beta chain gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16103410 11402 Tcrb T cell receptor beta chain gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15770700 11402 Tcrb T cell receptor beta chain gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:8104709 11402 Tcrb T cell receptor beta chain gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18997009 11402 Tcrb T cell receptor beta chain gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:1359428 11402 Tcrb T cell receptor beta chain gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:19017966 11402 Tcrb T cell receptor beta chain gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9075933 11402 Tcrb T cell receptor beta chain gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:16103410 11402 Tcrb T cell receptor beta chain gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 11402 Tcrb T cell receptor beta chain gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:15770700 11402 Tcrb T cell receptor beta chain gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15770700 11402 Tcrb T cell receptor beta chain gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9075933 11402 Tcrb T cell receptor beta chain gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10850719 11402 Tcrb T cell receptor beta chain gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:16272283 11402 Tcrb T cell receptor beta chain gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17617584 11402 Tcrb T cell receptor beta chain gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:1359428 11402 Tcrb T cell receptor beta chain gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17617584 11402 Tcrb T cell receptor beta chain gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15964276 11402 Tcrb T cell receptor beta chain gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19380806 11402 Tcrb T cell receptor beta chain gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1359428 11402 Tcrb T cell receptor beta chain gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17617584 11402 Tcrb T cell receptor beta chain gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17617584 11402 Tcrb T cell receptor beta chain gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1359428 11402 Tcrb T cell receptor beta chain gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19380806 11402 Tcrb T cell receptor beta chain gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19380806 11402 Tcrb T cell receptor beta chain gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:19017966 11402 Tcrb T cell receptor beta chain gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0008188 abnormal transitional stage B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0008348 absent gamma-delta T cells IAGP N RGD:5509061 20141003 MGI PMID:17617584 11402 Tcrb T cell receptor beta chain gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11937563 11402 Tcrb T cell receptor beta chain gene MP:0008758 abnormal T cell receptor beta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:12530977 11402 Tcrb T cell receptor beta chain gene MP:0008758 abnormal T cell receptor beta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:18250443 11402 Tcrb T cell receptor beta chain gene MP:0008758 abnormal T cell receptor beta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:19070901 11402 Tcrb T cell receptor beta chain gene MP:0008758 abnormal T cell receptor beta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:19380806 11402 Tcrb T cell receptor beta chain gene MP:0009925 increased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0010229 increased transitional stage T3 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22341446 11402 Tcrb T cell receptor beta chain gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 11402 Tcrb T cell receptor beta chain gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:22585710 11403 Tcrg T cell receptor gamma chain gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:18242214 11403 Tcrg T cell receptor gamma chain gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16034115 11403 Tcrg T cell receptor gamma chain gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16034115 11403 Tcrg T cell receptor gamma chain gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16034115 11403 Tcrg T cell receptor gamma chain gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:16034115 11403 Tcrg T cell receptor gamma chain gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9497293 11403 Tcrg T cell receptor gamma chain gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:16034115 11403 Tcrg T cell receptor gamma chain gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:18242214 11403 Tcrg T cell receptor gamma chain gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:18242214 11403 Tcrg T cell receptor gamma chain gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16034115 11403 Tcrg T cell receptor gamma chain gene MP:0005074 impaired granulocyte bactericidal activity IAGP N RGD:5509061 20141003 MGI PMID:16034115 11403 Tcrg T cell receptor gamma chain gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16034115 11403 Tcrg T cell receptor gamma chain gene MP:0008348 absent gamma-delta T cells IAGP N RGD:5509061 20141003 MGI PMID:18242214 11403 Tcrg T cell receptor gamma chain gene MP:0008356 abnormal gamma-delta T cell differentiation IAGP N RGD:5509061 20221201 MGI PMID:11911829 11403 Tcrg T cell receptor gamma chain gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18242214 11403 Tcrg T cell receptor gamma chain gene MP:0008757 abnormal T cell receptor gamma chain V-J recombination IAGP N RGD:5509061 20141003 MGI PMID:18378791 11403 Tcrg T cell receptor gamma chain gene MP:0008757 abnormal T cell receptor gamma chain V-J recombination IAGP N RGD:5509061 20221201 MGI PMID:11911829 11404 Tead2 TEA domain family member 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 11404 Tead2 TEA domain family member 2 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:20596238 11404 Tead2 TEA domain family member 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17868131 11404 Tead2 TEA domain family member 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 11404 Tead2 TEA domain family member 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20596238 11404 Tead2 TEA domain family member 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17868131 11404 Tead2 TEA domain family member 2 gene MP:0013217 abnormal posterior definitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 11404 Tead2 TEA domain family member 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:18332127 11405 Tmbim6 transmembrane BAX inhibitor motif containing 6 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:15304216 11405 Tmbim6 transmembrane BAX inhibitor motif containing 6 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15304216 11406 Trf transferrin gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:3681112 11406 Trf transferrin gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210520 MGI 11406 Trf transferrin gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 11406 Trf transferrin gene MP:0001513 limb grasping IEA N RGD:5509061 20210520 MGI 11406 Trf transferrin gene MP:0001523 impaired righting response IEA N RGD:5509061 20210520 MGI 11406 Trf transferrin gene MP:0001565 abnormal circulating phosphate level IEA N RGD:5509061 20210520 MGI 11406 Trf transferrin gene MP:0001589 abnormal mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 11406 Trf transferrin gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 11406 Trf transferrin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:3681112 11406 Trf transferrin gene MP:0002424 abnormal reticulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:3681112 11406 Trf transferrin gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 11406 Trf transferrin gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:3681112 11406 Trf transferrin gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:3681112 11406 Trf transferrin gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:3681112 11406 Trf transferrin gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:3681112 11406 Trf transferrin gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:3681112 11406 Trf transferrin gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:3681112 11406 Trf transferrin gene MP:0003717 pallor IEA N RGD:5509061 20201022 MGI 11406 Trf transferrin gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20200514 MGI 11406 Trf transferrin gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 11406 Trf transferrin gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:3681112 11406 Trf transferrin gene MP:0005638 hemochromatosis IAGP N RGD:5509061 20141003 MGI PMID:3681112 11406 Trf transferrin gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:3681112 11406 Trf transferrin gene MP:0008387 hypochromic anemia IAGP N RGD:5509061 20141003 MGI PMID:3681112 11406 Trf transferrin gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:3681112 11406 Trf transferrin gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 11406 Trf transferrin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:3681112 11406 Trf transferrin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11407 Tff3 trefoil factor 3, intestinal gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8824194 11407 Tff3 trefoil factor 3, intestinal gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:8824194 11407 Tff3 trefoil factor 3, intestinal gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:8824194 11408 Tg thyroglobulin gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:3803305 11408 Tg thyroglobulin gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 11408 Tg thyroglobulin gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:1508304 11408 Tg thyroglobulin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:1508304 11408 Tg thyroglobulin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:3803305 11408 Tg thyroglobulin gene MP:0001265 decreased body size IAGP N RGD:5509061 20151119 MGI PMID:22724066 11408 Tg thyroglobulin gene MP:0001265 decreased body size IAGP N RGD:5509061 20210930 MGI PMID:33905568 11408 Tg thyroglobulin gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 11408 Tg thyroglobulin gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 11408 Tg thyroglobulin gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20190502 MGI 11408 Tg thyroglobulin gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:3803305 11408 Tg thyroglobulin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20151119 MGI PMID:22724066 11408 Tg thyroglobulin gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 11408 Tg thyroglobulin gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:1508304 11408 Tg thyroglobulin gene MP:0002427 disproportionate dwarf IEA N RGD:5509061 20111116 MGI 11408 Tg thyroglobulin gene MP:0002492 decreased IgE level IEA N RGD:5509061 20181025 MGI 11408 Tg thyroglobulin gene MP:0002497 increased IgE level IEA N RGD:5509061 20190411 MGI 11408 Tg thyroglobulin gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20230601 MGI 11408 Tg thyroglobulin gene MP:0002764 short tibia IEA N RGD:5509061 20181025 MGI 11408 Tg thyroglobulin gene MP:0002865 increased growth rate IEA N RGD:5509061 20111116 MGI 11408 Tg thyroglobulin gene MP:0003109 short femur IEA N RGD:5509061 20181025 MGI 11408 Tg thyroglobulin gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181025 MGI 11408 Tg thyroglobulin gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20181025 MGI 11408 Tg thyroglobulin gene MP:0004696 abnormal thyroid follicle morphology IEA N RGD:5509061 20111116 MGI 11408 Tg thyroglobulin gene MP:0004697 abnormal thyroid follicular cell morphology IEA N RGD:5509061 20111116 MGI 11408 Tg thyroglobulin gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 11408 Tg thyroglobulin gene MP:0005017 decreased B cell number IEA N RGD:5509061 20181025 MGI 11408 Tg thyroglobulin gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:3803305 11408 Tg thyroglobulin gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 11408 Tg thyroglobulin gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:3803305 11408 Tg thyroglobulin gene MP:0005425 increased macrophage cell number IEA N RGD:5509061 20190411 MGI 11408 Tg thyroglobulin gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:3803305 11408 Tg thyroglobulin gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:3803305 11408 Tg thyroglobulin gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190411 MGI 11408 Tg thyroglobulin gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190411 MGI 11408 Tg thyroglobulin gene MP:0008167 increased B-1a cell number IEA N RGD:5509061 20190411 MGI 11408 Tg thyroglobulin gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20190411 MGI 11408 Tg thyroglobulin gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20181025 MGI 11408 Tg thyroglobulin gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 11408 Tg thyroglobulin gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 11408 Tg thyroglobulin gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20231207 MGI 11408 Tg thyroglobulin gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190411 MGI 11408 Tg thyroglobulin gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20190411 MGI 11408 Tg thyroglobulin gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20190411 MGI 11408 Tg thyroglobulin gene MP:0014143 decreased body fat mass IEA N RGD:5509061 20181025 MGI 11411 Tgfa transforming growth factor alpha gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20111208 MGI 11411 Tgfa transforming growth factor alpha gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:8477444 11411 Tgfa transforming growth factor alpha gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0000396 increased curvature of hairs IAGP N RGD:5509061 20141003 MGI PMID:8477444 11411 Tgfa transforming growth factor alpha gene MP:0000402 abnormal zigzag hair morphology IEA N RGD:5509061 20111116 MGI 11411 Tgfa transforming growth factor alpha gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:10331984 11411 Tgfa transforming growth factor alpha gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:15456865 11411 Tgfa transforming growth factor alpha gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:8477444 11411 Tgfa transforming growth factor alpha gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:10331984 11411 Tgfa transforming growth factor alpha gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:11438495 11411 Tgfa transforming growth factor alpha gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:10331984 11411 Tgfa transforming growth factor alpha gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:10331984 11411 Tgfa transforming growth factor alpha gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:10331984 11411 Tgfa transforming growth factor alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11438495 11411 Tgfa transforming growth factor alpha gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10331984 11411 Tgfa transforming growth factor alpha gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 11411 Tgfa transforming growth factor alpha gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:10331984 11411 Tgfa transforming growth factor alpha gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:8477444 11411 Tgfa transforming growth factor alpha gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0001278 kinked vibrissae IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0001279 wavy vibrissae IEA N RGD:5509061 20111116 MGI 11411 Tgfa transforming growth factor alpha gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10331984 11411 Tgfa transforming growth factor alpha gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:13358719 11411 Tgfa transforming growth factor alpha gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:10331984 11411 Tgfa transforming growth factor alpha gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:13358719 11411 Tgfa transforming growth factor alpha gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15456865 11411 Tgfa transforming growth factor alpha gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:8477444 11411 Tgfa transforming growth factor alpha gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:8477444 11411 Tgfa transforming growth factor alpha gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:10331984 11411 Tgfa transforming growth factor alpha gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:13358719 11411 Tgfa transforming growth factor alpha gene MP:0001316 cornea scarring IAGP N RGD:5509061 20141003 MGI PMID:13358719 11411 Tgfa transforming growth factor alpha gene MP:0001316 cornea scarring IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20111116 MGI 11411 Tgfa transforming growth factor alpha gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10331984 11411 Tgfa transforming growth factor alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15366372 11411 Tgfa transforming growth factor alpha gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:13358719 11411 Tgfa transforming growth factor alpha gene MP:0002074 abnormal hair texture IEA N RGD:5509061 20111116 MGI 11411 Tgfa transforming growth factor alpha gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20111116 MGI 11411 Tgfa transforming growth factor alpha gene MP:0002580 duodenal lesions IAGP N RGD:5509061 20141003 MGI PMID:11438495 11411 Tgfa transforming growth factor alpha gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:11438495 11411 Tgfa transforming growth factor alpha gene MP:0003095 abnormal cornea stroma development IAGP N RGD:5509061 20141003 MGI PMID:13358719 11411 Tgfa transforming growth factor alpha gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11438495 11411 Tgfa transforming growth factor alpha gene MP:0003671 abnormal eyelid aperture IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0003704 abnormal hair follicle development IEA N RGD:5509061 20111116 MGI 11411 Tgfa transforming growth factor alpha gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0003812 abnormal hair medulla IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0004285 absent Descemet membrane IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:15366372 11411 Tgfa transforming growth factor alpha gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:11438495 11411 Tgfa transforming growth factor alpha gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0006194 keratoconjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:13358719 11411 Tgfa transforming growth factor alpha gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:10331984 11411 Tgfa transforming growth factor alpha gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20141225 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:13358719 11411 Tgfa transforming growth factor alpha gene MP:0009272 decreased guard hair length IEA N RGD:5509061 20111116 MGI 11411 Tgfa transforming growth factor alpha gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20141225 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0009742 increased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:13358719 11411 Tgfa transforming growth factor alpha gene MP:0010709 absent eye anterior chamber IAGP N RGD:5509061 20141225 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0013389 Meibomian gland hypoplasia IAGP N RGD:5509061 20141225 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0013396 eyelid hyperplasia IAGP N RGD:5509061 20141225 MGI PMID:8477445 11411 Tgfa transforming growth factor alpha gene MP:0013716 hypolactation IAGP N RGD:5509061 20150402 MGI PMID:10331984 11411 Tgfa transforming growth factor alpha gene MP:0030175 orbicularis oculi muscle hypoplasia IAGP N RGD:5509061 20171005 MGI PMID:8477445 11414 Th tyrosine hydroxylase gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:7715703 11414 Th tyrosine hydroxylase gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10212311 11414 Th tyrosine hydroxylase gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10212311 11414 Th tyrosine hydroxylase gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:7715703 11414 Th tyrosine hydroxylase gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:8548806 11414 Th tyrosine hydroxylase gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:7592982 11414 Th tyrosine hydroxylase gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:21040852 11414 Th tyrosine hydroxylase gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:21040852 11414 Th tyrosine hydroxylase gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:21040852 11414 Th tyrosine hydroxylase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7715703 11414 Th tyrosine hydroxylase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8548806 11414 Th tyrosine hydroxylase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:8548806 11414 Th tyrosine hydroxylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10212311 11414 Th tyrosine hydroxylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12704806 11414 Th tyrosine hydroxylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18701681 11414 Th tyrosine hydroxylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7715703 11414 Th tyrosine hydroxylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8548806 11414 Th tyrosine hydroxylase gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20180913 MGI PMID:22764207 11414 Th tyrosine hydroxylase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10518589 11414 Th tyrosine hydroxylase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10518589 11414 Th tyrosine hydroxylase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22711987 11414 Th tyrosine hydroxylase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:8548806 11414 Th tyrosine hydroxylase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10518589 11414 Th tyrosine hydroxylase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10518589 11414 Th tyrosine hydroxylase gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:10518589 11414 Th tyrosine hydroxylase gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:21040852 11414 Th tyrosine hydroxylase gene MP:0001428 adipsia IAGP N RGD:5509061 20141003 MGI PMID:8548806 11414 Th tyrosine hydroxylase gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:8548806 11414 Th tyrosine hydroxylase gene MP:0001443 poor grooming IAGP N RGD:5509061 20141003 MGI PMID:8548806 11414 Th tyrosine hydroxylase gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:10704516 11414 Th tyrosine hydroxylase gene MP:0001462 abnormal avoidance learning behavior IAGP N RGD:5509061 20141003 MGI PMID:19864633 11414 Th tyrosine hydroxylase gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:10518589 11414 Th tyrosine hydroxylase gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:8548806 11414 Th tyrosine hydroxylase gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:7715703 11414 Th tyrosine hydroxylase gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:7592982 11414 Th tyrosine hydroxylase gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:21040852 11414 Th tyrosine hydroxylase gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21040852 11414 Th tyrosine hydroxylase gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:21040852 11414 Th tyrosine hydroxylase gene MP:0002039 increased neuroblastoma incidence IAGP N RGD:5509061 20180913 MGI PMID:22764207 11414 Th tyrosine hydroxylase gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:10704516 11414 Th tyrosine hydroxylase gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:10704516 11414 Th tyrosine hydroxylase gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18701681 11414 Th tyrosine hydroxylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10518589 11414 Th tyrosine hydroxylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22711987 11414 Th tyrosine hydroxylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8548806 11414 Th tyrosine hydroxylase gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:22764243 11414 Th tyrosine hydroxylase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15452869 11414 Th tyrosine hydroxylase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16876957 11414 Th tyrosine hydroxylase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19116659 11414 Th tyrosine hydroxylase gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:18701681 11414 Th tyrosine hydroxylase gene MP:0002316 anoxia IAGP N RGD:5509061 20141003 MGI PMID:7592982 11414 Th tyrosine hydroxylase gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:10518589 11414 Th tyrosine hydroxylase gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0002798 abnormal active avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:10704516 11414 Th tyrosine hydroxylase gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:10704516 11414 Th tyrosine hydroxylase gene MP:0002822 catalepsy IAGP N RGD:5509061 20141003 MGI PMID:10518589 11414 Th tyrosine hydroxylase gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:10212311 11414 Th tyrosine hydroxylase gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:7715703 11414 Th tyrosine hydroxylase gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:10212311 11414 Th tyrosine hydroxylase gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:7715703 11414 Th tyrosine hydroxylase gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:18701681 11414 Th tyrosine hydroxylase gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22711987 11414 Th tyrosine hydroxylase gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:22711987 11414 Th tyrosine hydroxylase gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:8548806 11414 Th tyrosine hydroxylase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22711987 11414 Th tyrosine hydroxylase gene MP:0003897 abnormal ST segment IAGP N RGD:5509061 20141003 MGI PMID:7592982 11414 Th tyrosine hydroxylase gene MP:0003908 decreased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:8548806 11414 Th tyrosine hydroxylase gene MP:0003962 abnormal adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:10212311 11414 Th tyrosine hydroxylase gene MP:0003962 abnormal adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:7592982 11414 Th tyrosine hydroxylase gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:10212311 11414 Th tyrosine hydroxylase gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:10704516 11414 Th tyrosine hydroxylase gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:18701681 11414 Th tyrosine hydroxylase gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:7592982 11414 Th tyrosine hydroxylase gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:12704806 11414 Th tyrosine hydroxylase gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:22711987 11414 Th tyrosine hydroxylase gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:22764243 11414 Th tyrosine hydroxylase gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:7592982 11414 Th tyrosine hydroxylase gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:7715703 11414 Th tyrosine hydroxylase gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:10518589 11414 Th tyrosine hydroxylase gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22764243 11414 Th tyrosine hydroxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:10212311 11414 Th tyrosine hydroxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:12704806 11414 Th tyrosine hydroxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:18701681 11414 Th tyrosine hydroxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:19864633 11414 Th tyrosine hydroxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22027820 11414 Th tyrosine hydroxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22711987 11414 Th tyrosine hydroxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22764243 11414 Th tyrosine hydroxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:7592982 11414 Th tyrosine hydroxylase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:8548806 11414 Th tyrosine hydroxylase gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20141003 MGI PMID:18701681 11414 Th tyrosine hydroxylase gene MP:0008504 abnormal adrenal chromaffin cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22711987 11414 Th tyrosine hydroxylase gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22711987 11414 Th tyrosine hydroxylase gene MP:0009078 adrenal gland hyperplasia IAGP N RGD:5509061 20180913 MGI PMID:22764207 11414 Th tyrosine hydroxylase gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:22711987 11414 Th tyrosine hydroxylase gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:10518589 11414 Th tyrosine hydroxylase gene MP:0010017 visceral vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:10212311 11414 Th tyrosine hydroxylase gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:7715703 11414 Th tyrosine hydroxylase gene MP:0010021 heart vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:10212311 11414 Th tyrosine hydroxylase gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:12704806 11414 Th tyrosine hydroxylase gene MP:0010072 increased pruritus IAGP N RGD:5509061 20141003 MGI PMID:21040852 11414 Th tyrosine hydroxylase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18701681 11414 Th tyrosine hydroxylase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7715703 11414 Th tyrosine hydroxylase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7592982 11414 Th tyrosine hydroxylase gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7592982 11414 Th tyrosine hydroxylase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10212311 11414 Th tyrosine hydroxylase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16876957 11414 Th tyrosine hydroxylase gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20210325 MGI PMID:33208756 11414 Th tyrosine hydroxylase gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10212311 11414 Th tyrosine hydroxylase gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7715703 11414 Th tyrosine hydroxylase gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7592982 11414 Th tyrosine hydroxylase gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7715703 11414 Th tyrosine hydroxylase gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:10518589 11414 Th tyrosine hydroxylase gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:10518589 11414 Th tyrosine hydroxylase gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:16723393 11414 Th tyrosine hydroxylase gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20180920 MGI PMID:12704806 11414 Th tyrosine hydroxylase gene MP:0020843 abnormal type I cell of carotid body physiology IAGP N RGD:5509061 20240801 MGI PMID:38706960 11414 Th tyrosine hydroxylase gene MP:0031252 abnormal physiological response to hypoxia IAGP N RGD:5509061 20210729 MGI PMID:31848220 11414 Th tyrosine hydroxylase gene MP:0031613 fetal cardiomyocyte disarray IAGP N RGD:5509061 20240509 MGI PMID:7715703 11414 Th tyrosine hydroxylase gene MP:0031614 fetal cardiomyocyte vacuoles IAGP N RGD:5509061 20240509 MGI PMID:7715703 11415 Thra thyroid hormone receptor alpha gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:11739587 11415 Thra thyroid hormone receptor alpha gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20201022 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16051666 11415 Thra thyroid hormone receptor alpha gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0000478 delayed intestine development IAGP N RGD:5509061 20141003 MGI PMID:9927422 11415 Thra thyroid hormone receptor alpha gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11416151 11415 Thra thyroid hormone receptor alpha gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9927422 11415 Thra thyroid hormone receptor alpha gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:11416151 11415 Thra thyroid hormone receptor alpha gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:16131613 11415 Thra thyroid hormone receptor alpha gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20190725 MGI PMID:29205102 11415 Thra thyroid hormone receptor alpha gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16131613 11415 Thra thyroid hormone receptor alpha gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11734632 11415 Thra thyroid hormone receptor alpha gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11734632 11415 Thra thyroid hormone receptor alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12356724 11415 Thra thyroid hormone receptor alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15304375 11415 Thra thyroid hormone receptor alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17210747 11415 Thra thyroid hormone receptor alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9927422 11415 Thra thyroid hormone receptor alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11739587 11415 Thra thyroid hormone receptor alpha gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16131613 11415 Thra thyroid hormone receptor alpha gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0001399 hyperactivity IEA N RGD:5509061 20170105 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:16131613 11415 Thra thyroid hormone receptor alpha gene MP:0001469 abnormal contextual conditioning behavior IEA N RGD:5509061 20210128 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0001488 increased startle reflex IEA N RGD:5509061 20181227 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210128 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0001513 limb grasping IEA N RGD:5509061 20181227 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0001542 abnormal bone strength IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:12356724 11415 Thra thyroid hormone receptor alpha gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11726557 11415 Thra thyroid hormone receptor alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16051666 11415 Thra thyroid hormone receptor alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9927422 11415 Thra thyroid hormone receptor alpha gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:11734632 11415 Thra thyroid hormone receptor alpha gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11734632 11415 Thra thyroid hormone receptor alpha gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11734632 11415 Thra thyroid hormone receptor alpha gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11739587 11415 Thra thyroid hormone receptor alpha gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11734632 11415 Thra thyroid hormone receptor alpha gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11734632 11415 Thra thyroid hormone receptor alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9927422 11415 Thra thyroid hormone receptor alpha gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:15304375 11415 Thra thyroid hormone receptor alpha gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0002608 increased hematocrit IEA N RGD:5509061 20211021 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:17210747 11415 Thra thyroid hormone receptor alpha gene MP:0002710 increased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:16051666 11415 Thra thyroid hormone receptor alpha gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20190725 MGI PMID:29205102 11415 Thra thyroid hormone receptor alpha gene MP:0002876 abnormal thyroid gland physiology IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16051666 11415 Thra thyroid hormone receptor alpha gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16051666 11415 Thra thyroid hormone receptor alpha gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9927422 11415 Thra thyroid hormone receptor alpha gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0003109 short femur IAGP N RGD:5509061 20190725 MGI PMID:29205102 11415 Thra thyroid hormone receptor alpha gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11739587 11415 Thra thyroid hormone receptor alpha gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:9430637 11415 Thra thyroid hormone receptor alpha gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:16131613 11415 Thra thyroid hormone receptor alpha gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20739404 11415 Thra thyroid hormone receptor alpha gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:16051666 11415 Thra thyroid hormone receptor alpha gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16051666 11415 Thra thyroid hormone receptor alpha gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20190725 MGI PMID:29205102 11415 Thra thyroid hormone receptor alpha gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16051666 11415 Thra thyroid hormone receptor alpha gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11416151 11415 Thra thyroid hormone receptor alpha gene MP:0003498 thyroid gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9927422 11415 Thra thyroid hormone receptor alpha gene MP:0003499 thyroid gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9927422 11415 Thra thyroid hormone receptor alpha gene MP:0003502 increased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:11734632 11415 Thra thyroid hormone receptor alpha gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:9430637 11415 Thra thyroid hormone receptor alpha gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:12576486 11415 Thra thyroid hormone receptor alpha gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:16051666 11415 Thra thyroid hormone receptor alpha gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20181227 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16051666 11415 Thra thyroid hormone receptor alpha gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16051666 11415 Thra thyroid hormone receptor alpha gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11739587 11415 Thra thyroid hormone receptor alpha gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20210520 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0003965 abnormal pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:17210747 11415 Thra thyroid hormone receptor alpha gene MP:0003971 abnormal thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:16051666 11415 Thra thyroid hormone receptor alpha gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16803873 11415 Thra thyroid hormone receptor alpha gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:11739587 11415 Thra thyroid hormone receptor alpha gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11739587 11415 Thra thyroid hormone receptor alpha gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11739587 11415 Thra thyroid hormone receptor alpha gene MP:0004437 decreased cochlear outer hair cell electromotility IAGP N RGD:5509061 20141003 MGI PMID:11739587 11415 Thra thyroid hormone receptor alpha gene MP:0004591 enlarged tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:11739587 11415 Thra thyroid hormone receptor alpha gene MP:0004664 delayed inner ear development IAGP N RGD:5509061 20141003 MGI PMID:11739587 11415 Thra thyroid hormone receptor alpha gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11726557 11415 Thra thyroid hormone receptor alpha gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9927422 11415 Thra thyroid hormone receptor alpha gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11739587 11415 Thra thyroid hormone receptor alpha gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17210747 11415 Thra thyroid hormone receptor alpha gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15304375 11415 Thra thyroid hormone receptor alpha gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0005119 decreased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12576486 11415 Thra thyroid hormone receptor alpha gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11734632 11415 Thra thyroid hormone receptor alpha gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12576486 11415 Thra thyroid hormone receptor alpha gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15601836 11415 Thra thyroid hormone receptor alpha gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:9927422 11415 Thra thyroid hormone receptor alpha gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17210747 11415 Thra thyroid hormone receptor alpha gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:17210747 11415 Thra thyroid hormone receptor alpha gene MP:0005135 increased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17210747 11415 Thra thyroid hormone receptor alpha gene MP:0005135 increased thyroid-stimulating hormone level IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:17210747 11415 Thra thyroid hormone receptor alpha gene MP:0005138 decreased prolactin level IAGP N RGD:5509061 20141003 MGI PMID:17210747 11415 Thra thyroid hormone receptor alpha gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11159823 11415 Thra thyroid hormone receptor alpha gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:9430637 11415 Thra thyroid hormone receptor alpha gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:15601836 11415 Thra thyroid hormone receptor alpha gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:11726557 11415 Thra thyroid hormone receptor alpha gene MP:0005474 increased triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:9927422 11415 Thra thyroid hormone receptor alpha gene MP:0005474 increased triiodothyronine level IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0005474 increased triiodothyronine level IAGP N RGD:5509061 20190725 MGI PMID:29205102 11415 Thra thyroid hormone receptor alpha gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:12576486 11415 Thra thyroid hormone receptor alpha gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:15601836 11415 Thra thyroid hormone receptor alpha gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:9927422 11415 Thra thyroid hormone receptor alpha gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:11159823 11415 Thra thyroid hormone receptor alpha gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:11726557 11415 Thra thyroid hormone receptor alpha gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:12576486 11415 Thra thyroid hormone receptor alpha gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:11726557 11415 Thra thyroid hormone receptor alpha gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:11734632 11415 Thra thyroid hormone receptor alpha gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:12576486 11415 Thra thyroid hormone receptor alpha gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:15601836 11415 Thra thyroid hormone receptor alpha gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:20739404 11415 Thra thyroid hormone receptor alpha gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:9430637 11415 Thra thyroid hormone receptor alpha gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210826 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11416151 11415 Thra thyroid hormone receptor alpha gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11159823 11415 Thra thyroid hormone receptor alpha gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16051666 11415 Thra thyroid hormone receptor alpha gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20141003 MGI PMID:9927422 11415 Thra thyroid hormone receptor alpha gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11416151 11415 Thra thyroid hormone receptor alpha gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11416151 11415 Thra thyroid hormone receptor alpha gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20190725 MGI PMID:29205102 11415 Thra thyroid hormone receptor alpha gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20190725 MGI PMID:29205102 11415 Thra thyroid hormone receptor alpha gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:17327419 11415 Thra thyroid hormone receptor alpha gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11739587 11415 Thra thyroid hormone receptor alpha gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17065405 11415 Thra thyroid hormone receptor alpha gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0010122 abnormal bone mineral content IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:11159823 11415 Thra thyroid hormone receptor alpha gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:16051666 11415 Thra thyroid hormone receptor alpha gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0010964 increased compact bone volume IAGP N RGD:5509061 20150827 MGI PMID:24914936 11415 Thra thyroid hormone receptor alpha gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12356724 11415 Thra thyroid hormone receptor alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17622582 11415 Thra thyroid hormone receptor alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20190725 MGI PMID:29205102 11415 Thra thyroid hormone receptor alpha gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12356724 11415 Thra thyroid hormone receptor alpha gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:12869545 11415 Thra thyroid hormone receptor alpha gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:21914860 11415 Thra thyroid hormone receptor alpha gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20181227 MGI 11415 Thra thyroid hormone receptor alpha gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11739587 11415 Thra thyroid hormone receptor alpha gene MP:0013618 decreased areal bone mineral density IAGP N RGD:5509061 20150319 MGI PMID:11731613 11415 Thra thyroid hormone receptor alpha gene MP:0013958 decreased small intestine length IAGP N RGD:5509061 20160414 MGI PMID:9927422 11415 Thra thyroid hormone receptor alpha gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20160414 MGI PMID:11416151 11415 Thra thyroid hormone receptor alpha gene MP:0014091 abnormal tectorial membrane striated-sheet matrix morphology IAGP N RGD:5509061 20160421 MGI PMID:11739587 11415 Thra thyroid hormone receptor alpha gene MP:0014296 delayed skeletal maturation IAGP N RGD:5509061 20230824 MGI PMID:9927422 11415 Thra thyroid hormone receptor alpha gene MP:0030020 decreased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:15304375 11415 Thra thyroid hormone receptor alpha gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:16051666 11415 Thra thyroid hormone receptor alpha gene MP:0030388 large fontanelles IAGP N RGD:5509061 20171207 MGI PMID:16051666 11417 Thrsp thyroid hormone responsive gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:15890771 11417 Thrsp thyroid hormone responsive gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15890771 11417 Thrsp thyroid hormone responsive gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:15890771 11417 Thrsp thyroid hormone responsive gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15890771 11418 Thy1 thymus cell antigen 1, theta gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20180719 MGI PMID:8587606 11418 Thy1 thymus cell antigen 1, theta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:12031407 11418 Thy1 thymus cell antigen 1, theta gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20180719 MGI PMID:16049324 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16037568 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23524300 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:23144462 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:23524300 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15262835 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:23144462 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:11560951 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:16778336 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:11560951 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:19128402 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15262835 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19806081 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:11560951 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15262835 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16037568 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11560952 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:15322543 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15322543 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:11560952 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11560951 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:19806081 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11560951 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23144462 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11560951 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16778336 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23524300 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:11560951 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:11560951 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15262835 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:16037568 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15262835 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:16037568 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23524300 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:16778336 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16037568 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:18408187 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:15262835 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0003824 decreased left ventricle developed pressure IAGP N RGD:5509061 20141003 MGI PMID:15262835 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:16037568 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15322543 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16037568 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:15262835 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:16037568 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16037568 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:16778336 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12147610 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:11560951 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12147610 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20150319 MGI PMID:24736588 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:15322543 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20150319 MGI PMID:24736588 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:23524300 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15262835 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16037568 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0006026 dilated terminal bronchiole tube IAGP N RGD:5509061 20141003 MGI PMID:14499643 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:14499643 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:19128402 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0006083 abnormal blood vessel elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:23524300 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:16037568 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0006237 abnormal choroid vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18408187 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:11560952 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15322543 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20150319 MGI PMID:24736588 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0008987 abnormal liver lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:15322543 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15322543 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16037568 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210617 MGI PMID:23144462 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:23144462 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0009870 abnormal abdominal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:23144462 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20160421 MGI 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0010139 aortitis IAGP N RGD:5509061 20141003 MGI PMID:23144462 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0010659 abdominal aorta aneurysm IAGP N RGD:5509061 20141003 MGI PMID:23144462 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0011031 abnormal branching involved in terminal bronchiole morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:14499643 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0014474 decreased pulmonary alveolus wall thickness IAGP N RGD:5509061 20240704 MGI PMID:19128402 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20180125 MGI PMID:24736588 11419 Timp3 tissue inhibitor of metalloproteinase 3 gene MP:0031274 increased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:23144462 11420 Nkx2-1 NK2 homeobox 1 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:17522155 11420 Nkx2-1 NK2 homeobox 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:21345181 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:10208743 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:10401665 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17164424 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10401665 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12829717 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17182767 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11854318 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17182767 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17182767 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20141003 MGI PMID:17182767 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:17182767 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:12829717 11420 Nkx2-1 NK2 homeobox 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:21345181 11420 Nkx2-1 NK2 homeobox 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20160114 MGI 11420 Nkx2-1 NK2 homeobox 1 gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12829717 11420 Nkx2-1 NK2 homeobox 1 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10208743 11420 Nkx2-1 NK2 homeobox 1 gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:10208743 11420 Nkx2-1 NK2 homeobox 1 gene MP:0002295 abnormal pulmonary circulation IAGP N RGD:5509061 20141003 MGI PMID:10208743 11420 Nkx2-1 NK2 homeobox 1 gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12399445 11420 Nkx2-1 NK2 homeobox 1 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:15581879 11420 Nkx2-1 NK2 homeobox 1 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:16601074 11420 Nkx2-1 NK2 homeobox 1 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:10208743 11420 Nkx2-1 NK2 homeobox 1 gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:10208743 11420 Nkx2-1 NK2 homeobox 1 gene MP:0003421 abnormal thyroid gland development IAGP N RGD:5509061 20141003 MGI PMID:10401665 11420 Nkx2-1 NK2 homeobox 1 gene MP:0003421 abnormal thyroid gland development IAGP N RGD:5509061 20141003 MGI PMID:21345181 11420 Nkx2-1 NK2 homeobox 1 gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141003 MGI PMID:21345181 11420 Nkx2-1 NK2 homeobox 1 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:17182767 11420 Nkx2-1 NK2 homeobox 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12829717 11420 Nkx2-1 NK2 homeobox 1 gene MP:0004551 decreased tracheal cartilage ring number IAGP N RGD:5509061 20141003 MGI PMID:10208743 11420 Nkx2-1 NK2 homeobox 1 gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16601074 11420 Nkx2-1 NK2 homeobox 1 gene MP:0004733 abnormal thoracic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:10208743 11420 Nkx2-1 NK2 homeobox 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12399445 11420 Nkx2-1 NK2 homeobox 1 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11854318 11420 Nkx2-1 NK2 homeobox 1 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:16601074 11420 Nkx2-1 NK2 homeobox 1 gene MP:0005314 absent thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:21345181 11420 Nkx2-1 NK2 homeobox 1 gene MP:0005314 absent thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0005315 absent pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:21345181 11420 Nkx2-1 NK2 homeobox 1 gene MP:0005315 absent pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:10208743 11420 Nkx2-1 NK2 homeobox 1 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10208743 11420 Nkx2-1 NK2 homeobox 1 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17164424 11420 Nkx2-1 NK2 homeobox 1 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:17182767 11420 Nkx2-1 NK2 homeobox 1 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:17182767 11420 Nkx2-1 NK2 homeobox 1 gene MP:0009008 delayed estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:17182767 11420 Nkx2-1 NK2 homeobox 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16601074 11420 Nkx2-1 NK2 homeobox 1 gene MP:0010812 absent type II pneumocytes IAGP N RGD:5509061 20141003 MGI PMID:10208743 11420 Nkx2-1 NK2 homeobox 1 gene MP:0010814 absent alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:17164424 11420 Nkx2-1 NK2 homeobox 1 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:12829717 11420 Nkx2-1 NK2 homeobox 1 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:17164424 11420 Nkx2-1 NK2 homeobox 1 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:12829717 11420 Nkx2-1 NK2 homeobox 1 gene MP:0010898 abnormal pulmonary alveolus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17164424 11420 Nkx2-1 NK2 homeobox 1 gene MP:0010901 abnormal pulmonary alveolar parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0010911 abnormal pulmonary acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:12829717 11420 Nkx2-1 NK2 homeobox 1 gene MP:0010943 abnormal bronchus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:17164424 11420 Nkx2-1 NK2 homeobox 1 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12829717 11420 Nkx2-1 NK2 homeobox 1 gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10208743 11420 Nkx2-1 NK2 homeobox 1 gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0011034 impaired branching involved in respiratory bronchiole morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12829717 11420 Nkx2-1 NK2 homeobox 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17164424 11420 Nkx2-1 NK2 homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12829717 11420 Nkx2-1 NK2 homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21345181 11420 Nkx2-1 NK2 homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:17164424 11420 Nkx2-1 NK2 homeobox 1 gene MP:0011145 abnormal mesenchymal cell differentiation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:12829717 11420 Nkx2-1 NK2 homeobox 1 gene MP:0012684 abnormal pleural cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:10208743 11420 Nkx2-1 NK2 homeobox 1 gene MP:0012684 abnormal pleural cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0013337 abnormal adenohypophysis development IAGP N RGD:5509061 20141218 MGI PMID:9806931 11420 Nkx2-1 NK2 homeobox 1 gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:21345181 11420 Nkx2-1 NK2 homeobox 1 gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:9806931 11420 Nkx2-1 NK2 homeobox 1 gene MP:0013352 abnormal Rathke's pouch apoptosis IAGP N RGD:5509061 20141218 MGI PMID:9806931 11420 Nkx2-1 NK2 homeobox 1 gene MP:0013490 absent infundibular recess of third ventricle IAGP N RGD:5509061 20150212 MGI PMID:21345181 11420 Nkx2-1 NK2 homeobox 1 gene MP:0014198 absent pituitary infundibular stalk IAGP N RGD:5509061 20160526 MGI PMID:9806931 11420 Nkx2-1 NK2 homeobox 1 gene MP:0014269 decreased testes secretion IAGP N RGD:5509061 20230810 MGI PMID:12399445 11420 Nkx2-1 NK2 homeobox 1 gene MP:0020556 abnormal ventromedial hypothalamic nucleus morphology IAGP N RGD:5509061 20180315 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0020558 decreased ventromedial hypothalamic nucleus size IAGP N RGD:5509061 20180315 MGI PMID:8557195 11420 Nkx2-1 NK2 homeobox 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:17182767 11421 Tk1 thymidine kinase 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0003504 thyroid gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0003991 arteriosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0004035 abnormal sublingual gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0009161 pancreatic acinar cell zymogen granule accumulation IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0010138 arteritis IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10029690 11421 Tk1 thymidine kinase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12559842 11421 Tk1 thymidine kinase 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10029690 11421 Tk1 thymidine kinase 1 gene MP:0031071 lymph node atrophy IAGP N RGD:5509061 20200618 MGI PMID:12559842 11422 Tle4 transducin-like enhancer of split 4 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0000492 abnormal rectum morphology IEA N RGD:5509061 20210520 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0000599 enlarged liver IEA N RGD:5509061 20210826 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0002083 premature death IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20210128 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20231207 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220519 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20231207 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 11422 Tle4 transducin-like enhancer of split 4 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0010132 decreased DN2 thymocyte number IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0011816 decreased pre-pro B cell number IAGP N RGD:5509061 20160225 MGI PMID:25153823 11422 Tle4 transducin-like enhancer of split 4 gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:25153823 11425 Tmpo thymopoietin gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:18849980 11425 Tmpo thymopoietin gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:18849980 11425 Tmpo thymopoietin gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18849980 11425 Tmpo thymopoietin gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18849980 11425 Tmpo thymopoietin gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18849980 11425 Tmpo thymopoietin gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18849980 11425 Tmpo thymopoietin gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18849980 11429 Tnf tumor necrosis factor gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20180719 MGI PMID:17266397 11429 Tnf tumor necrosis factor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20180719 MGI PMID:17266397 11429 Tnf tumor necrosis factor gene MP:0000160 kyphosis IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:15832287 11429 Tnf tumor necrosis factor gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:8671586 11429 Tnf tumor necrosis factor gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:9368616 11429 Tnf tumor necrosis factor gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180719 MGI PMID:12496444 11429 Tnf tumor necrosis factor gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180719 MGI PMID:15832287 11429 Tnf tumor necrosis factor gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180719 MGI PMID:16037568 11429 Tnf tumor necrosis factor gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:15199130 11429 Tnf tumor necrosis factor gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20180719 MGI PMID:15199130 11429 Tnf tumor necrosis factor gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20180719 MGI PMID:15199130 11429 Tnf tumor necrosis factor gene MP:0000414 alopecia IAGP N RGD:5509061 20180719 MGI PMID:15366373 11429 Tnf tumor necrosis factor gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20180719 MGI PMID:23977323 11429 Tnf tumor necrosis factor gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180719 MGI PMID:16406654 11429 Tnf tumor necrosis factor gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180719 MGI PMID:10878371 11429 Tnf tumor necrosis factor gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20180719 MGI PMID:10586051 11429 Tnf tumor necrosis factor gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20180719 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20180719 MGI PMID:8671586 11429 Tnf tumor necrosis factor gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20180719 MGI PMID:9368616 11429 Tnf tumor necrosis factor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180719 MGI PMID:12486099 11429 Tnf tumor necrosis factor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180719 MGI PMID:9368616 11429 Tnf tumor necrosis factor gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20180719 MGI PMID:11672536 11429 Tnf tumor necrosis factor gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20180719 MGI PMID:16751399 11429 Tnf tumor necrosis factor gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20180719 MGI PMID:9177215 11429 Tnf tumor necrosis factor gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20180719 MGI PMID:9368616 11429 Tnf tumor necrosis factor gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20180719 MGI PMID:18299349 11429 Tnf tumor necrosis factor gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20180719 MGI PMID:10411942 11429 Tnf tumor necrosis factor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20180719 MGI PMID:18832037 11429 Tnf tumor necrosis factor gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20180719 MGI PMID:12496444 11429 Tnf tumor necrosis factor gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20210826 MGI PMID:33210082 11429 Tnf tumor necrosis factor gene MP:0001194 dermatitis IAGP N RGD:5509061 20180719 MGI PMID:23453632 11429 Tnf tumor necrosis factor gene MP:0001212 skin lesions IAGP N RGD:5509061 20180719 MGI PMID:12496444 11429 Tnf tumor necrosis factor gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20180719 MGI PMID:15199130 11429 Tnf tumor necrosis factor gene MP:0001218 thin epidermis IAGP N RGD:5509061 20180719 MGI PMID:15199130 11429 Tnf tumor necrosis factor gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20180719 MGI PMID:15199130 11429 Tnf tumor necrosis factor gene MP:0001257 increased body length IAGP N RGD:5509061 20180719 MGI PMID:16406654 11429 Tnf tumor necrosis factor gene MP:0001260 increased body weight IAGP N RGD:5509061 20180719 MGI PMID:16406654 11429 Tnf tumor necrosis factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180719 MGI PMID:10204494 11429 Tnf tumor necrosis factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180719 MGI PMID:9287059 11429 Tnf tumor necrosis factor gene MP:0001263 weight loss IAGP N RGD:5509061 20180719 MGI PMID:12486099 11429 Tnf tumor necrosis factor gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20180719 MGI PMID:21436282 11429 Tnf tumor necrosis factor gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20180719 MGI PMID:11063830 11429 Tnf tumor necrosis factor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180719 MGI PMID:11063830 11429 Tnf tumor necrosis factor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180719 MGI PMID:10411942 11429 Tnf tumor necrosis factor gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20180719 MGI PMID:11063830 11429 Tnf tumor necrosis factor gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20180719 MGI PMID:12163535 11429 Tnf tumor necrosis factor gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20180719 MGI PMID:10411942 11429 Tnf tumor necrosis factor gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20180719 MGI PMID:12486099 11429 Tnf tumor necrosis factor gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20180719 MGI PMID:24727475 11429 Tnf tumor necrosis factor gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20180719 MGI PMID:15664162 11429 Tnf tumor necrosis factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180719 MGI PMID:15199130 11429 Tnf tumor necrosis factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20210826 MGI PMID:33210082 11429 Tnf tumor necrosis factor gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20180719 MGI PMID:11672536 11429 Tnf tumor necrosis factor gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20180719 MGI PMID:9223320 11429 Tnf tumor necrosis factor gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20180719 MGI PMID:9834074 11429 Tnf tumor necrosis factor gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20180719 MGI PMID:8671586 11429 Tnf tumor necrosis factor gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20180719 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20180719 MGI PMID:18256672 11429 Tnf tumor necrosis factor gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20180719 MGI PMID:9223320 11429 Tnf tumor necrosis factor gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20180719 MGI PMID:8671586 11429 Tnf tumor necrosis factor gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20180719 MGI PMID:10204494 11429 Tnf tumor necrosis factor gene MP:0001844 autoimmune response IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20180719 MGI PMID:15334086 11429 Tnf tumor necrosis factor gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20180719 MGI PMID:18439426 11429 Tnf tumor necrosis factor gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20180719 MGI PMID:23453632 11429 Tnf tumor necrosis factor gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20180719 MGI PMID:18439426 11429 Tnf tumor necrosis factor gene MP:0001861 lung inflammation IAGP N RGD:5509061 20180719 MGI PMID:12496444 11429 Tnf tumor necrosis factor gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20180719 MGI PMID:10395330 11429 Tnf tumor necrosis factor gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20180719 MGI PMID:23977107 11429 Tnf tumor necrosis factor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180719 MGI PMID:23977107 11429 Tnf tumor necrosis factor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180719 MGI PMID:9287059 11429 Tnf tumor necrosis factor gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20180719 MGI PMID:16039576 11429 Tnf tumor necrosis factor gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:10204494 11429 Tnf tumor necrosis factor gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:12486099 11429 Tnf tumor necrosis factor gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:15334086 11429 Tnf tumor necrosis factor gene MP:0002083 premature death IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0002083 premature death IAGP N RGD:5509061 20210826 MGI PMID:33210082 11429 Tnf tumor necrosis factor gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180719 MGI PMID:9287059 11429 Tnf tumor necrosis factor gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20180719 MGI PMID:9177215 11429 Tnf tumor necrosis factor gene MP:0002345 abnormal lymph node primary follicle morphology IAGP N RGD:5509061 20180719 MGI PMID:11672536 11429 Tnf tumor necrosis factor gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20180719 MGI PMID:11672536 11429 Tnf tumor necrosis factor gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20180719 MGI PMID:12115620 11429 Tnf tumor necrosis factor gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20180719 MGI PMID:9368616 11429 Tnf tumor necrosis factor gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20180719 MGI PMID:8671586 11429 Tnf tumor necrosis factor gene MP:0002363 abnormal spleen marginal sinus morphology IAGP N RGD:5509061 20180719 MGI PMID:16751399 11429 Tnf tumor necrosis factor gene MP:0002363 abnormal spleen marginal sinus morphology IAGP N RGD:5509061 20180719 MGI PMID:9368616 11429 Tnf tumor necrosis factor gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20180719 MGI PMID:11672536 11429 Tnf tumor necrosis factor gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20180719 MGI PMID:15832287 11429 Tnf tumor necrosis factor gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20180719 MGI PMID:16751399 11429 Tnf tumor necrosis factor gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20180719 MGI PMID:9177215 11429 Tnf tumor necrosis factor gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20180719 MGI PMID:9368616 11429 Tnf tumor necrosis factor gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20180719 MGI PMID:15832287 11429 Tnf tumor necrosis factor gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20180719 MGI PMID:16751399 11429 Tnf tumor necrosis factor gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20180719 MGI PMID:9426403 11429 Tnf tumor necrosis factor gene MP:0002392 abnormal Peyer's patch T cell area morphology IAGP N RGD:5509061 20180719 MGI PMID:15832287 11429 Tnf tumor necrosis factor gene MP:0002392 abnormal Peyer's patch T cell area morphology IAGP N RGD:5509061 20180719 MGI PMID:16751399 11429 Tnf tumor necrosis factor gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:15832287 11429 Tnf tumor necrosis factor gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:15664162 11429 Tnf tumor necrosis factor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:15814712 11429 Tnf tumor necrosis factor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:16015367 11429 Tnf tumor necrosis factor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:16751399 11429 Tnf tumor necrosis factor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:8671586 11429 Tnf tumor necrosis factor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:8879212 11429 Tnf tumor necrosis factor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:9130661 11429 Tnf tumor necrosis factor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:9223320 11429 Tnf tumor necrosis factor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:9834074 11429 Tnf tumor necrosis factor gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20180719 MGI PMID:18439426 11429 Tnf tumor necrosis factor gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20180719 MGI PMID:9426403 11429 Tnf tumor necrosis factor gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20180719 MGI PMID:12496444 11429 Tnf tumor necrosis factor gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20180719 MGI PMID:9368616 11429 Tnf tumor necrosis factor gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20180719 MGI PMID:12496444 11429 Tnf tumor necrosis factor gene MP:0002494 increased IgM level IAGP N RGD:5509061 20180719 MGI PMID:9834074 11429 Tnf tumor necrosis factor gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20180719 MGI PMID:12486099 11429 Tnf tumor necrosis factor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180719 MGI PMID:16406654 11429 Tnf tumor necrosis factor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180719 MGI PMID:9287059 11429 Tnf tumor necrosis factor gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20180719 MGI PMID:15199130 11429 Tnf tumor necrosis factor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20180719 MGI PMID:18832037 11429 Tnf tumor necrosis factor gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180719 MGI PMID:9287059 11429 Tnf tumor necrosis factor gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20180719 MGI PMID:16037568 11429 Tnf tumor necrosis factor gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20180719 MGI PMID:11063830 11429 Tnf tumor necrosis factor gene MP:0002791 steatorrhea IAGP N RGD:5509061 20180719 MGI PMID:23977107 11429 Tnf tumor necrosis factor gene MP:0002816 colitis IAGP N RGD:5509061 20180719 MGI PMID:12727921 11429 Tnf tumor necrosis factor gene MP:0002816 colitis IAGP N RGD:5509061 20180719 MGI PMID:21804564 11429 Tnf tumor necrosis factor gene MP:0002816 colitis IAGP N RGD:5509061 20210826 MGI PMID:33210082 11429 Tnf tumor necrosis factor gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20180719 MGI PMID:10586051 11429 Tnf tumor necrosis factor gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20180719 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20180719 MGI PMID:15832287 11429 Tnf tumor necrosis factor gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20180719 MGI PMID:8671586 11429 Tnf tumor necrosis factor gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20180719 MGI PMID:9368616 11429 Tnf tumor necrosis factor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20180719 MGI PMID:16406654 11429 Tnf tumor necrosis factor gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0002933 joint inflammation IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180719 MGI PMID:16406654 11429 Tnf tumor necrosis factor gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20180719 MGI PMID:15366373 11429 Tnf tumor necrosis factor gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20180719 MGI PMID:16287858 11429 Tnf tumor necrosis factor gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20180719 MGI PMID:18250193 11429 Tnf tumor necrosis factor gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20180719 MGI PMID:18439426 11429 Tnf tumor necrosis factor gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20210826 MGI PMID:33210082 11429 Tnf tumor necrosis factor gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20180719 MGI PMID:15334086 11429 Tnf tumor necrosis factor gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20180719 MGI PMID:9223320 11429 Tnf tumor necrosis factor gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20180719 MGI PMID:9426403 11429 Tnf tumor necrosis factor gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0003064 decreased coping response IAGP N RGD:5509061 20180719 MGI PMID:11063830 11429 Tnf tumor necrosis factor gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20180719 MGI PMID:15199130 11429 Tnf tumor necrosis factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0003278 esophageal inflammation IAGP N RGD:5509061 20210826 MGI PMID:33210082 11429 Tnf tumor necrosis factor gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20180719 MGI PMID:23977323 11429 Tnf tumor necrosis factor gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20180719 MGI PMID:10204494 11429 Tnf tumor necrosis factor gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20180719 MGI PMID:12486099 11429 Tnf tumor necrosis factor gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20180719 MGI PMID:15366373 11429 Tnf tumor necrosis factor gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20180719 MGI PMID:18250193 11429 Tnf tumor necrosis factor gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20180719 MGI PMID:23977107 11429 Tnf tumor necrosis factor gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20180719 MGI PMID:23977323 11429 Tnf tumor necrosis factor gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20180719 MGI PMID:9834074 11429 Tnf tumor necrosis factor gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20180719 MGI PMID:10204494 11429 Tnf tumor necrosis factor gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20180719 MGI PMID:15905096 11429 Tnf tumor necrosis factor gene MP:0003674 oxidative stress IAGP N RGD:5509061 20180719 MGI PMID:24727475 11429 Tnf tumor necrosis factor gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20180719 MGI PMID:10639149 11429 Tnf tumor necrosis factor gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20180719 MGI PMID:18439426 11429 Tnf tumor necrosis factor gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20180719 MGI PMID:18832037 11429 Tnf tumor necrosis factor gene MP:0004357 long tibia IAGP N RGD:5509061 20180719 MGI PMID:16406654 11429 Tnf tumor necrosis factor gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20180719 MGI PMID:10395330 11429 Tnf tumor necrosis factor gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180719 MGI PMID:10064079 11429 Tnf tumor necrosis factor gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180719 MGI PMID:11672536 11429 Tnf tumor necrosis factor gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180719 MGI PMID:12471141 11429 Tnf tumor necrosis factor gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180719 MGI PMID:9348316 11429 Tnf tumor necrosis factor gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180719 MGI PMID:9565643 11429 Tnf tumor necrosis factor gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20180719 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180719 MGI PMID:18832037 11429 Tnf tumor necrosis factor gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20180719 MGI PMID:18832037 11429 Tnf tumor necrosis factor gene MP:0004947 skin inflammation IAGP N RGD:5509061 20180719 MGI PMID:12496444 11429 Tnf tumor necrosis factor gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20180719 MGI PMID:16406654 11429 Tnf tumor necrosis factor gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20180719 MGI PMID:17266397 11429 Tnf tumor necrosis factor gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20180719 MGI PMID:18250468 11429 Tnf tumor necrosis factor gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20180719 MGI PMID:18439426 11429 Tnf tumor necrosis factor gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:15832287 11429 Tnf tumor necrosis factor gene MP:0005014 increased B cell number IAGP N RGD:5509061 20180719 MGI PMID:8671586 11429 Tnf tumor necrosis factor gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20180719 MGI PMID:8671586 11429 Tnf tumor necrosis factor gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20180719 MGI PMID:9006341 11429 Tnf tumor necrosis factor gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20180719 MGI PMID:12496444 11429 Tnf tumor necrosis factor gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20180719 MGI PMID:15832287 11429 Tnf tumor necrosis factor gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20180719 MGI PMID:12486099 11429 Tnf tumor necrosis factor gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20180719 MGI PMID:18256672 11429 Tnf tumor necrosis factor gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20180719 MGI PMID:18256672 11429 Tnf tumor necrosis factor gene MP:0005150 cachexia IAGP N RGD:5509061 20180719 MGI PMID:15334086 11429 Tnf tumor necrosis factor gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20180719 MGI PMID:10698075 11429 Tnf tumor necrosis factor gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20180719 MGI PMID:10586051 11429 Tnf tumor necrosis factor gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20180719 MGI PMID:9426403 11429 Tnf tumor necrosis factor gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20180719 MGI PMID:9287059 11429 Tnf tumor necrosis factor gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20180719 MGI PMID:15664162 11429 Tnf tumor necrosis factor gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20180719 MGI PMID:9223320 11429 Tnf tumor necrosis factor gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20180719 MGI PMID:23977107 11429 Tnf tumor necrosis factor gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20180719 MGI PMID:9287059 11429 Tnf tumor necrosis factor gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20180719 MGI PMID:18439426 11429 Tnf tumor necrosis factor gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20180719 MGI PMID:18854186 11429 Tnf tumor necrosis factor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180719 MGI PMID:9287059 11429 Tnf tumor necrosis factor gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20180719 MGI PMID:16037568 11429 Tnf tumor necrosis factor gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20180719 MGI PMID:8879212 11429 Tnf tumor necrosis factor gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180719 MGI PMID:16406654 11429 Tnf tumor necrosis factor gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180719 MGI PMID:23977107 11429 Tnf tumor necrosis factor gene MP:0005667 abnormal circulating leptin level IAGP N RGD:5509061 20180719 MGI PMID:23977107 11429 Tnf tumor necrosis factor gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20180719 MGI PMID:9287059 11429 Tnf tumor necrosis factor gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20180719 MGI PMID:12486099 11429 Tnf tumor necrosis factor gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20180719 MGI PMID:12486099 11429 Tnf tumor necrosis factor gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20180719 MGI PMID:12486099 11429 Tnf tumor necrosis factor gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20180719 MGI PMID:12496444 11429 Tnf tumor necrosis factor gene MP:0006087 increased body mass index IAGP N RGD:5509061 20180719 MGI PMID:16406654 11429 Tnf tumor necrosis factor gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0006167 eyelid edema IAGP N RGD:5509061 20180719 MGI PMID:23453632 11429 Tnf tumor necrosis factor gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:8671586 11429 Tnf tumor necrosis factor gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:9368616 11429 Tnf tumor necrosis factor gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:18854186 11429 Tnf tumor necrosis factor gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:12486099 11429 Tnf tumor necrosis factor gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20180719 MGI PMID:12486099 11429 Tnf tumor necrosis factor gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20180719 MGI PMID:12496444 11429 Tnf tumor necrosis factor gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20180719 MGI PMID:23977323 11429 Tnf tumor necrosis factor gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20180719 MGI PMID:23977107 11429 Tnf tumor necrosis factor gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20180719 MGI PMID:15832287 11429 Tnf tumor necrosis factor gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20180719 MGI PMID:16751399 11429 Tnf tumor necrosis factor gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20180719 MGI PMID:9177215 11429 Tnf tumor necrosis factor gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20180719 MGI PMID:9368616 11429 Tnf tumor necrosis factor gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20180719 MGI PMID:15832287 11429 Tnf tumor necrosis factor gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20180719 MGI PMID:9368616 11429 Tnf tumor necrosis factor gene MP:0008179 absent germinal center B cells IAGP N RGD:5509061 20180719 MGI PMID:10586051 11429 Tnf tumor necrosis factor gene MP:0008197 abnormal follicular dendritic cell physiology IAGP N RGD:5509061 20180719 MGI PMID:9223320 11429 Tnf tumor necrosis factor gene MP:0008200 decreased follicular dendritic cell number IAGP N RGD:5509061 20180719 MGI PMID:16751399 11429 Tnf tumor necrosis factor gene MP:0008200 decreased follicular dendritic cell number IAGP N RGD:5509061 20180719 MGI PMID:9368616 11429 Tnf tumor necrosis factor gene MP:0008201 absent follicular dendritic cells IAGP N RGD:5509061 20180719 MGI PMID:10586051 11429 Tnf tumor necrosis factor gene MP:0008201 absent follicular dendritic cells IAGP N RGD:5509061 20180719 MGI PMID:15832287 11429 Tnf tumor necrosis factor gene MP:0008201 absent follicular dendritic cells IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0008201 absent follicular dendritic cells IAGP N RGD:5509061 20180719 MGI PMID:9177215 11429 Tnf tumor necrosis factor gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20180719 MGI PMID:10586051 11429 Tnf tumor necrosis factor gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20180719 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0008241 abnormal metallophilic macrophage morphology IAGP N RGD:5509061 20180719 MGI PMID:11672536 11429 Tnf tumor necrosis factor gene MP:0008241 abnormal metallophilic macrophage morphology IAGP N RGD:5509061 20180719 MGI PMID:16751399 11429 Tnf tumor necrosis factor gene MP:0008343 abnormal gamma-delta T cell morphology IAGP N RGD:5509061 20180719 MGI PMID:21419662 11429 Tnf tumor necrosis factor gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20180719 MGI PMID:18439426 11429 Tnf tumor necrosis factor gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20180719 MGI PMID:17218256 11429 Tnf tumor necrosis factor gene MP:0008399 abnormal alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20180719 MGI PMID:18439426 11429 Tnf tumor necrosis factor gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20180719 MGI PMID:10411942 11429 Tnf tumor necrosis factor gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20180719 MGI PMID:21436282 11429 Tnf tumor necrosis factor gene MP:0008464 absent peripheral lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:10586051 11429 Tnf tumor necrosis factor gene MP:0008465 absent mesenteric lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20180719 MGI PMID:12115620 11429 Tnf tumor necrosis factor gene MP:0008471 abnormal spleen primary B follicle morphology IAGP N RGD:5509061 20180719 MGI PMID:11672536 11429 Tnf tumor necrosis factor gene MP:0008471 abnormal spleen primary B follicle morphology IAGP N RGD:5509061 20180719 MGI PMID:16751399 11429 Tnf tumor necrosis factor gene MP:0008471 abnormal spleen primary B follicle morphology IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0008471 abnormal spleen primary B follicle morphology IAGP N RGD:5509061 20180719 MGI PMID:8879212 11429 Tnf tumor necrosis factor gene MP:0008471 abnormal spleen primary B follicle morphology IAGP N RGD:5509061 20180719 MGI PMID:9368616 11429 Tnf tumor necrosis factor gene MP:0008473 abnormal spleen follicular dendritic cell network IAGP N RGD:5509061 20180719 MGI PMID:11672536 11429 Tnf tumor necrosis factor gene MP:0008473 abnormal spleen follicular dendritic cell network IAGP N RGD:5509061 20180719 MGI PMID:16751399 11429 Tnf tumor necrosis factor gene MP:0008473 abnormal spleen follicular dendritic cell network IAGP N RGD:5509061 20180719 MGI PMID:9287059 11429 Tnf tumor necrosis factor gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20180719 MGI PMID:11672536 11429 Tnf tumor necrosis factor gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20180719 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20180719 MGI PMID:16751399 11429 Tnf tumor necrosis factor gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20180719 MGI PMID:8879212 11429 Tnf tumor necrosis factor gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20180719 MGI PMID:9223320 11429 Tnf tumor necrosis factor gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20180719 MGI PMID:9426403 11429 Tnf tumor necrosis factor gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20180719 MGI PMID:10586051 11429 Tnf tumor necrosis factor gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20180719 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20180719 MGI PMID:16705172 11429 Tnf tumor necrosis factor gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20180719 MGI PMID:11672536 11429 Tnf tumor necrosis factor gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20180719 MGI PMID:11672536 11429 Tnf tumor necrosis factor gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:18256672 11429 Tnf tumor necrosis factor gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:9834074 11429 Tnf tumor necrosis factor gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20180719 MGI PMID:18256672 11429 Tnf tumor necrosis factor gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20180719 MGI PMID:9834074 11429 Tnf tumor necrosis factor gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20180719 MGI PMID:9834074 11429 Tnf tumor necrosis factor gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20180719 MGI PMID:21436282 11429 Tnf tumor necrosis factor gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20180719 MGI PMID:21436282 11429 Tnf tumor necrosis factor gene MP:0008523 absent lymph node germinal center IAGP N RGD:5509061 20180719 MGI PMID:9426403 11429 Tnf tumor necrosis factor gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20180719 MGI PMID:10204494 11429 Tnf tumor necrosis factor gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20180719 MGI PMID:23977107 11429 Tnf tumor necrosis factor gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20180719 MGI PMID:23977323 11429 Tnf tumor necrosis factor gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20180719 MGI PMID:15664162 11429 Tnf tumor necrosis factor gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20180719 MGI PMID:10204494 11429 Tnf tumor necrosis factor gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20180719 MGI PMID:18854186 11429 Tnf tumor necrosis factor gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20180719 MGI PMID:9130661 11429 Tnf tumor necrosis factor gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:12496444 11429 Tnf tumor necrosis factor gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:12727921 11429 Tnf tumor necrosis factor gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:18250468 11429 Tnf tumor necrosis factor gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:18256672 11429 Tnf tumor necrosis factor gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:9834074 11429 Tnf tumor necrosis factor gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20180719 MGI PMID:9426403 11429 Tnf tumor necrosis factor gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20180719 MGI PMID:9834074 11429 Tnf tumor necrosis factor gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20180719 MGI PMID:9426403 11429 Tnf tumor necrosis factor gene MP:0008639 decreased circulating interleukin-1 alpha level IAGP N RGD:5509061 20180719 MGI PMID:9426403 11429 Tnf tumor necrosis factor gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20180719 MGI PMID:9426403 11429 Tnf tumor necrosis factor gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20180719 MGI PMID:12727921 11429 Tnf tumor necrosis factor gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20180719 MGI PMID:18854186 11429 Tnf tumor necrosis factor gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20180719 MGI PMID:12727921 11429 Tnf tumor necrosis factor gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20180719 MGI PMID:12471141 11429 Tnf tumor necrosis factor gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20180719 MGI PMID:15664162 11429 Tnf tumor necrosis factor gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20180719 MGI PMID:11672536 11429 Tnf tumor necrosis factor gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20180719 MGI PMID:15664162 11429 Tnf tumor necrosis factor gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20180719 MGI PMID:9130661 11429 Tnf tumor necrosis factor gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20180719 MGI PMID:9223320 11429 Tnf tumor necrosis factor gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20180719 MGI PMID:9426403 11429 Tnf tumor necrosis factor gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20180719 MGI PMID:10204494 11429 Tnf tumor necrosis factor gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20180719 MGI PMID:12496444 11429 Tnf tumor necrosis factor gene MP:0008852 retina neovascularization IMP N RGD:7394795|PMID:19342600 20131105 RGD 11429 Tnf tumor necrosis factor gene MP:0008978 abnormal vagina weight IAGP N RGD:5509061 20180719 MGI PMID:10453074 11429 Tnf tumor necrosis factor gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20180719 MGI PMID:10453074 11429 Tnf tumor necrosis factor gene MP:0009384 cardiac valve regurgitation IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20180719 MGI PMID:18299349 11429 Tnf tumor necrosis factor gene MP:0009405 increased skeletal muscle fiber number IAGP N RGD:5509061 20180719 MGI PMID:18299349 11429 Tnf tumor necrosis factor gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20180719 MGI PMID:21804564 11429 Tnf tumor necrosis factor gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20180719 MGI PMID:16287858 11429 Tnf tumor necrosis factor gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20180719 MGI PMID:18250468 11429 Tnf tumor necrosis factor gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20180719 MGI PMID:18854186 11429 Tnf tumor necrosis factor gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20180719 MGI PMID:23977107 11429 Tnf tumor necrosis factor gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20180719 MGI PMID:23977323 11429 Tnf tumor necrosis factor gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20210826 MGI PMID:33210082 11429 Tnf tumor necrosis factor gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20180719 MGI PMID:10395330 11429 Tnf tumor necrosis factor gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:10586051 11429 Tnf tumor necrosis factor gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0009628 absent brachial lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:10586051 11429 Tnf tumor necrosis factor gene MP:0009628 absent brachial lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:10586051 11429 Tnf tumor necrosis factor gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0009633 absent cervical lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:10586051 11429 Tnf tumor necrosis factor gene MP:0009634 absent popliteal lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:10586051 11429 Tnf tumor necrosis factor gene MP:0009634 absent popliteal lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180719 MGI PMID:10698075 11429 Tnf tumor necrosis factor gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180719 MGI PMID:15664162 11429 Tnf tumor necrosis factor gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180719 MGI PMID:16015367 11429 Tnf tumor necrosis factor gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180719 MGI PMID:8671586 11429 Tnf tumor necrosis factor gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180719 MGI PMID:8671586 11429 Tnf tumor necrosis factor gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20180719 MGI PMID:9834074 11429 Tnf tumor necrosis factor gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:11063830 11429 Tnf tumor necrosis factor gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20180719 MGI PMID:23977107 11429 Tnf tumor necrosis factor gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20180719 MGI PMID:23977107 11429 Tnf tumor necrosis factor gene MP:0010222 abnormal T-helper 17 cell physiology IAGP N RGD:5509061 20180719 MGI PMID:23977107 11429 Tnf tumor necrosis factor gene MP:0010360 decreased liver free fatty acids level IAGP N RGD:5509061 20180719 MGI PMID:16406654 11429 Tnf tumor necrosis factor gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20180719 MGI PMID:16983719 11429 Tnf tumor necrosis factor gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20231221 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0010620 thick mitral valve IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20180719 MGI PMID:18854186 11429 Tnf tumor necrosis factor gene MP:0011079 decreased macrophage cytokine production IEA N RGD:5509061 20180719 MGI 11429 Tnf tumor necrosis factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:15199130 11429 Tnf tumor necrosis factor gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:19060883 11429 Tnf tumor necrosis factor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210826 MGI PMID:33210082 11429 Tnf tumor necrosis factor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20210826 MGI PMID:33210082 11429 Tnf tumor necrosis factor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:12771125 11429 Tnf tumor necrosis factor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:15199130 11429 Tnf tumor necrosis factor gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210826 MGI PMID:33210082 11429 Tnf tumor necrosis factor gene MP:0011572 abnormal aorta bulb morphology IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0011709 increased fibroblast cell migration IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0011804 increased cell migration IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0011929 abnormal aortic valve flow IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0013147 limb paralysis IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20180719 MGI PMID:21804564 11429 Tnf tumor necrosis factor gene MP:0014079 decreased small intestinal villus number IAGP N RGD:5509061 20180719 MGI PMID:23977323 11429 Tnf tumor necrosis factor gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20210826 MGI PMID:33210082 11429 Tnf tumor necrosis factor gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:12446781 11429 Tnf tumor necrosis factor gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:15664162 11429 Tnf tumor necrosis factor gene MP:0014269 decreased testes secretion IAGP N RGD:5509061 20230810 MGI PMID:18832037 11429 Tnf tumor necrosis factor gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20180906 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:8671586 11429 Tnf tumor necrosis factor gene MP:0020928 increased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:8671586 11429 Tnf tumor necrosis factor gene MP:0030332 accelerated temporomandibular joint osteoarthritis IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0030466 alveolar process atrophy IAGP N RGD:5509061 20180719 MGI PMID:17305866 11429 Tnf tumor necrosis factor gene MP:0030582 abnormal hair follicle placode formation IAGP N RGD:5509061 20180719 MGI PMID:15199130 11429 Tnf tumor necrosis factor gene MP:0030795 joint dislocation IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0030814 abnormal wrist joint morphology IAGP N RGD:5509061 20190117 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0031118 cardiovalvulitis IAGP N RGD:5509061 20210826 MGI PMID:33210082 11429 Tnf tumor necrosis factor gene MP:0031118 cardiovalvulitis IAGP N RGD:5509061 20240118 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0031124 aortic valve inflammation IAGP N RGD:5509061 20200917 MGI PMID:29618659 11429 Tnf tumor necrosis factor gene MP:0031124 aortic valve inflammation IAGP N RGD:5509061 20240118 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0031516 mitral valve inflammation IAGP N RGD:5509061 20240118 MGI PMID:26195802 11429 Tnf tumor necrosis factor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:29618659 11434 Tnnt2 troponin T2, cardiac gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:17556660 11434 Tnnt2 troponin T2, cardiac gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:18671960 11434 Tnnt2 troponin T2, cardiac gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17556660 11434 Tnnt2 troponin T2, cardiac gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20171012 MGI PMID:27936050 11434 Tnnt2 troponin T2, cardiac gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18671960 11434 Tnnt2 troponin T2, cardiac gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17556660 11434 Tnnt2 troponin T2, cardiac gene MP:0002083 premature death IAGP N RGD:5509061 20171012 MGI PMID:27936050 11434 Tnnt2 troponin T2, cardiac gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18671960 11434 Tnnt2 troponin T2, cardiac gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18671960 11434 Tnnt2 troponin T2, cardiac gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20171012 MGI PMID:27936050 11434 Tnnt2 troponin T2, cardiac gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20171012 MGI PMID:27936050 11434 Tnnt2 troponin T2, cardiac gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17556660 11434 Tnnt2 troponin T2, cardiac gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:17556660 11434 Tnnt2 troponin T2, cardiac gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:17556660 11434 Tnnt2 troponin T2, cardiac gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17556660 11434 Tnnt2 troponin T2, cardiac gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:18671960 11434 Tnnt2 troponin T2, cardiac gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:18671960 11434 Tnnt2 troponin T2, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:17556660 11434 Tnnt2 troponin T2, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20171012 MGI PMID:27936050 11434 Tnnt2 troponin T2, cardiac gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:18671960 11434 Tnnt2 troponin T2, cardiac gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:18671960 11434 Tnnt2 troponin T2, cardiac gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20171012 MGI PMID:27936050 11434 Tnnt2 troponin T2, cardiac gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20171012 MGI PMID:27936050 11434 Tnnt2 troponin T2, cardiac gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20171012 MGI PMID:27936050 11434 Tnnt2 troponin T2, cardiac gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17556660 11434 Tnnt2 troponin T2, cardiac gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20171012 MGI PMID:27936050 11434 Tnnt2 troponin T2, cardiac gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20171012 MGI PMID:27936050 11434 Tnnt2 troponin T2, cardiac gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0010553 prolonged HV interval IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18671960 11434 Tnnt2 troponin T2, cardiac gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18612386 11434 Tnnt2 troponin T2, cardiac gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20171012 MGI PMID:27936050 11434 Tnnt2 troponin T2, cardiac gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:17556660 11436 Tnnt3 troponin T3, skeletal, fast gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23775847 11436 Tnnt3 troponin T3, skeletal, fast gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:23775847 11436 Tnnt3 troponin T3, skeletal, fast gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:23775847 11436 Tnnt3 troponin T3, skeletal, fast gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23775847 11436 Tnnt3 troponin T3, skeletal, fast gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23775847 11436 Tnnt3 troponin T3, skeletal, fast gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23775847 11436 Tnnt3 troponin T3, skeletal, fast gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:23775847 11436 Tnnt3 troponin T3, skeletal, fast gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23775847 11436 Tnnt3 troponin T3, skeletal, fast gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:23775847 11436 Tnnt3 troponin T3, skeletal, fast gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:23775847 11436 Tnnt3 troponin T3, skeletal, fast gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23775847 11437 Tnp1 transition protein 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10781074 11437 Tnp1 transition protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10781074 11437 Tnp1 transition protein 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10781074 11437 Tnp1 transition protein 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10781074 11437 Tnp1 transition protein 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10781074 11437 Tnp1 transition protein 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:10781074 11437 Tnp1 transition protein 1 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:10781074 11437 Tnp1 transition protein 1 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:10781074 11438 Tnp2 transition protein 2 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:15685642 11438 Tnp2 transition protein 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15685642 11438 Tnp2 transition protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11385107 11438 Tnp2 transition protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15685642 11438 Tnp2 transition protein 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11585907 11438 Tnp2 transition protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11385107 11438 Tnp2 transition protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11585907 11438 Tnp2 transition protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12930723 11438 Tnp2 transition protein 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11385107 11438 Tnp2 transition protein 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11585907 11438 Tnp2 transition protein 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15685642 11438 Tnp2 transition protein 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11385107 11438 Tnp2 transition protein 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11585907 11438 Tnp2 transition protein 2 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:11385107 11438 Tnp2 transition protein 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:11385107 11438 Tnp2 transition protein 2 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20141003 MGI PMID:11385107 11438 Tnp2 transition protein 2 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11585907 11438 Tnp2 transition protein 2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:11585907 11438 Tnp2 transition protein 2 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20141003 MGI PMID:11585907 11438 Tnp2 transition protein 2 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:11385107 11438 Tnp2 transition protein 2 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:15685642 11438 Tnp2 transition protein 2 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191017 MGI PMID:15685642 11438 Tnp2 transition protein 2 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20200227 MGI PMID:15685642 11438 Tnp2 transition protein 2 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220811 MGI PMID:11585907 11440 Trp53 transformation related protein 53 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20190711 MGI PMID:29635765 11440 Trp53 transformation related protein 53 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:19620979 11440 Trp53 transformation related protein 53 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:14706339 11440 Trp53 transformation related protein 53 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:15607980 11440 Trp53 transformation related protein 53 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:16757976 11440 Trp53 transformation related protein 53 gene MP:0000088 short mandible IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22940690 11440 Trp53 transformation related protein 53 gene MP:0000111 cleft palate IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230309 MGI PMID:35593225 11440 Trp53 transformation related protein 53 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19620979 11440 Trp53 transformation related protein 53 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20230615 MGI PMID:23656786 11440 Trp53 transformation related protein 53 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20230622 MGI PMID:25671302 11440 Trp53 transformation related protein 53 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180830 MGI PMID:29479066 11440 Trp53 transformation related protein 53 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20180712 MGI PMID:29754823 11440 Trp53 transformation related protein 53 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20180830 MGI PMID:29479066 11440 Trp53 transformation related protein 53 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20180712 MGI PMID:29754823 11440 Trp53 transformation related protein 53 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20230615 MGI PMID:23656786 11440 Trp53 transformation related protein 53 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:16790550 11440 Trp53 transformation related protein 53 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:22044588 11440 Trp53 transformation related protein 53 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:15654339 11440 Trp53 transformation related protein 53 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:17070800 11440 Trp53 transformation related protein 53 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:17251932 11440 Trp53 transformation related protein 53 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:23798389 11440 Trp53 transformation related protein 53 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20180712 MGI PMID:29754823 11440 Trp53 transformation related protein 53 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21674502 11440 Trp53 transformation related protein 53 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20160225 MGI PMID:25144937 11440 Trp53 transformation related protein 53 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:16533502 11440 Trp53 transformation related protein 53 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:22044588 11440 Trp53 transformation related protein 53 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17363591 11440 Trp53 transformation related protein 53 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7504233 11440 Trp53 transformation related protein 53 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15607980 11440 Trp53 transformation related protein 53 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16597604 11440 Trp53 transformation related protein 53 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16616333 11440 Trp53 transformation related protein 53 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17070800 11440 Trp53 transformation related protein 53 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17332334 11440 Trp53 transformation related protein 53 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18591425 11440 Trp53 transformation related protein 53 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19176372 11440 Trp53 transformation related protein 53 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22228755 11440 Trp53 transformation related protein 53 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16616333 11440 Trp53 transformation related protein 53 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17000755 11440 Trp53 transformation related protein 53 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21487039 11440 Trp53 transformation related protein 53 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8943369 11440 Trp53 transformation related protein 53 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:23382688 11440 Trp53 transformation related protein 53 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20150326 MGI PMID:24979267 11440 Trp53 transformation related protein 53 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0000423 delayed hair regrowth IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0000423 delayed hair regrowth IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20150326 MGI PMID:24979267 11440 Trp53 transformation related protein 53 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:21549111 11440 Trp53 transformation related protein 53 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 11440 Trp53 transformation related protein 53 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:19620979 11440 Trp53 transformation related protein 53 gene MP:0000433 microcephaly IAGP N RGD:5509061 20190912 MGI PMID:31197172 11440 Trp53 transformation related protein 53 gene MP:0000433 microcephaly IAGP N RGD:5509061 20210204 MGI PMID:33110058 11440 Trp53 transformation related protein 53 gene MP:0000433 microcephaly IAGP N RGD:5509061 20230309 MGI PMID:35593225 11440 Trp53 transformation related protein 53 gene MP:0000433 microcephaly IAGP N RGD:5509061 20240718 MGI PMID:34237032 11440 Trp53 transformation related protein 53 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:22940690 11440 Trp53 transformation related protein 53 gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20141003 MGI PMID:16670198 11440 Trp53 transformation related protein 53 gene MP:0000445 short snout IAGP N RGD:5509061 20230309 MGI PMID:35593225 11440 Trp53 transformation related protein 53 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 11440 Trp53 transformation related protein 53 gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17363841 11440 Trp53 transformation related protein 53 gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17363841 11440 Trp53 transformation related protein 53 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20200820 MGI PMID:32728212 11440 Trp53 transformation related protein 53 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:12509446 11440 Trp53 transformation related protein 53 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20220721 MGI PMID:34376666 11440 Trp53 transformation related protein 53 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:16227443 11440 Trp53 transformation related protein 53 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0000569 abnormal digit pigmentation IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21674502 11440 Trp53 transformation related protein 53 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20141003 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 11440 Trp53 transformation related protein 53 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:19679647 11440 Trp53 transformation related protein 53 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:19234449 11440 Trp53 transformation related protein 53 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210422 MGI PMID:32381628 11440 Trp53 transformation related protein 53 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:18328429 11440 Trp53 transformation related protein 53 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:23166633 11440 Trp53 transformation related protein 53 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20160225 MGI PMID:25144937 11440 Trp53 transformation related protein 53 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16278673 11440 Trp53 transformation related protein 53 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20210422 MGI PMID:32381628 11440 Trp53 transformation related protein 53 gene MP:0000610 cholestasis IAGP N RGD:5509061 20141003 MGI PMID:15894267 11440 Trp53 transformation related protein 53 gene MP:0000621 increased salivary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17212342 11440 Trp53 transformation related protein 53 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:17212342 11440 Trp53 transformation related protein 53 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:17996864 11440 Trp53 transformation related protein 53 gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20473325 11440 Trp53 transformation related protein 53 gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:20585617 11440 Trp53 transformation related protein 53 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:16715125 11440 Trp53 transformation related protein 53 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:20473325 11440 Trp53 transformation related protein 53 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23166633 11440 Trp53 transformation related protein 53 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160225 MGI PMID:25144937 11440 Trp53 transformation related protein 53 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180830 MGI PMID:29479066 11440 Trp53 transformation related protein 53 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23665223 11440 Trp53 transformation related protein 53 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20160915 MGI PMID:23412344 11440 Trp53 transformation related protein 53 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20160225 MGI PMID:25144937 11440 Trp53 transformation related protein 53 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0000706 small thymus IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10077642 11440 Trp53 transformation related protein 53 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:10077642 11440 Trp53 transformation related protein 53 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:12555066 11440 Trp53 transformation related protein 53 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10911993 11440 Trp53 transformation related protein 53 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:18268034 11440 Trp53 transformation related protein 53 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20170817 MGI PMID:21804542 11440 Trp53 transformation related protein 53 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10783170 11440 Trp53 transformation related protein 53 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19477430 11440 Trp53 transformation related protein 53 gene MP:0000745 tremors IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:19176372 11440 Trp53 transformation related protein 53 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:10973261 11440 Trp53 transformation related protein 53 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:18948956 11440 Trp53 transformation related protein 53 gene MP:0000753 paralysis IAGP N RGD:5509061 20160804 MGI PMID:24141783 11440 Trp53 transformation related protein 53 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20190912 MGI PMID:31197172 11440 Trp53 transformation related protein 53 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20170314 MGI PMID:27815386 11440 Trp53 transformation related protein 53 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:21674502 11440 Trp53 transformation related protein 53 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:15821748 11440 Trp53 transformation related protein 53 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:16670198 11440 Trp53 transformation related protein 53 gene MP:0000865 absent cerebellum vermis IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21674502 11440 Trp53 transformation related protein 53 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15821748 11440 Trp53 transformation related protein 53 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16670198 11440 Trp53 transformation related protein 53 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12588846 11440 Trp53 transformation related protein 53 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16537918 11440 Trp53 transformation related protein 53 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21127973 11440 Trp53 transformation related protein 53 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21549111 11440 Trp53 transformation related protein 53 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:24209622 11440 Trp53 transformation related protein 53 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9171368 11440 Trp53 transformation related protein 53 gene MP:0000914 exencephaly IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0000914 exencephaly IAGP N RGD:5509061 20180809 MGI PMID:22815056 11440 Trp53 transformation related protein 53 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11914272 11440 Trp53 transformation related protein 53 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:12832489 11440 Trp53 transformation related protein 53 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21350561 11440 Trp53 transformation related protein 53 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:24209622 11440 Trp53 transformation related protein 53 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12208847 11440 Trp53 transformation related protein 53 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12642502 11440 Trp53 transformation related protein 53 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:22342750 11440 Trp53 transformation related protein 53 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:21124965 11440 Trp53 transformation related protein 53 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220224 MGI PMID:21277975 11440 Trp53 transformation related protein 53 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12642502 11440 Trp53 transformation related protein 53 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220224 MGI PMID:21277975 11440 Trp53 transformation related protein 53 gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:20585617 11440 Trp53 transformation related protein 53 gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16288012 11440 Trp53 transformation related protein 53 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:17299132 11440 Trp53 transformation related protein 53 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:22611036 11440 Trp53 transformation related protein 53 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20150910 MGI PMID:17676035 11440 Trp53 transformation related protein 53 gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:20697345 11440 Trp53 transformation related protein 53 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:11581300 11440 Trp53 transformation related protein 53 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:16757976 11440 Trp53 transformation related protein 53 gene MP:0001203 increased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:15735727 11440 Trp53 transformation related protein 53 gene MP:0001204 decreased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:10514395 11440 Trp53 transformation related protein 53 gene MP:0001204 decreased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:11581300 11440 Trp53 transformation related protein 53 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:15674344 11440 Trp53 transformation related protein 53 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:21502497 11440 Trp53 transformation related protein 53 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:23166633 11440 Trp53 transformation related protein 53 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20181129 MGI PMID:28878021 11440 Trp53 transformation related protein 53 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20150326 MGI PMID:24979267 11440 Trp53 transformation related protein 53 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20150326 MGI PMID:24979267 11440 Trp53 transformation related protein 53 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20181129 MGI PMID:28878021 11440 Trp53 transformation related protein 53 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15674344 11440 Trp53 transformation related protein 53 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10911993 11440 Trp53 transformation related protein 53 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16777961 11440 Trp53 transformation related protein 53 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19620979 11440 Trp53 transformation related protein 53 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20847051 11440 Trp53 transformation related protein 53 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151008 MGI PMID:24292676 11440 Trp53 transformation related protein 53 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190711 MGI PMID:29635765 11440 Trp53 transformation related protein 53 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210204 MGI PMID:33110058 11440 Trp53 transformation related protein 53 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230615 MGI PMID:23656786 11440 Trp53 transformation related protein 53 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230622 MGI PMID:25671302 11440 Trp53 transformation related protein 53 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16227443 11440 Trp53 transformation related protein 53 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22964582 11440 Trp53 transformation related protein 53 gene MP:0001263 weight loss IAGP N RGD:5509061 20150924 MGI PMID:25035393 11440 Trp53 transformation related protein 53 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16757976 11440 Trp53 transformation related protein 53 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17289567 11440 Trp53 transformation related protein 53 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:15894267 11440 Trp53 transformation related protein 53 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:16357136 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:10760284 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:12839925 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:15607980 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:15607981 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16288016 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16397237 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16585505 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17097565 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17349585 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17486075 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17607363 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17676052 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17906694 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18328429 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18559481 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:19767771 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:21674502 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:21799785 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22266220 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22341455 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22358843 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23047698 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23486187 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23845441 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:24029233 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:24120138 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20150319 MGI PMID:22617326 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20150514 MGI PMID:24784840 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20150910 MGI PMID:17676035 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20151008 MGI PMID:24292676 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160204 MGI PMID:25180607 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160204 MGI PMID:25815421 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160804 MGI PMID:24141783 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160915 MGI PMID:23412344 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20170601 MGI PMID:22190384 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20170608 MGI PMID:24711431 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20170615 MGI PMID:26411367 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20190516 MGI PMID:28790031 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20190523 MGI PMID:21282721 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20230608 MGI PMID:33594717 11440 Trp53 transformation related protein 53 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20230622 MGI PMID:25671302 11440 Trp53 transformation related protein 53 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:11956084 11440 Trp53 transformation related protein 53 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16473278 11440 Trp53 transformation related protein 53 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20160204 MGI PMID:25180607 11440 Trp53 transformation related protein 53 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20160915 MGI PMID:23412344 11440 Trp53 transformation related protein 53 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20180215 MGI PMID:28294115 11440 Trp53 transformation related protein 53 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20210506 MGI PMID:31794893 11440 Trp53 transformation related protein 53 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20240905 MGI PMID:38733589 11440 Trp53 transformation related protein 53 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201022 MGI 11440 Trp53 transformation related protein 53 gene MP:0001296 macrophthalmia IAGP N RGD:5509061 20141003 MGI PMID:20484573 11440 Trp53 transformation related protein 53 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:20484573 11440 Trp53 transformation related protein 53 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20210204 MGI PMID:33110058 11440 Trp53 transformation related protein 53 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:10885750 11440 Trp53 transformation related protein 53 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:20484573 11440 Trp53 transformation related protein 53 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:15231717 11440 Trp53 transformation related protein 53 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17363591 11440 Trp53 transformation related protein 53 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:15231717 11440 Trp53 transformation related protein 53 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10393064 11440 Trp53 transformation related protein 53 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10783170 11440 Trp53 transformation related protein 53 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10804210 11440 Trp53 transformation related protein 53 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10973261 11440 Trp53 transformation related protein 53 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17289567 11440 Trp53 transformation related protein 53 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18451155 11440 Trp53 transformation related protein 53 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18948956 11440 Trp53 transformation related protein 53 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19477430 11440 Trp53 transformation related protein 53 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0001393 ataxia IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10783170 11440 Trp53 transformation related protein 53 gene MP:0001394 circling IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0001396 unidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:18451155 11440 Trp53 transformation related protein 53 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180712 MGI PMID:29754823 11440 Trp53 transformation related protein 53 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10783170 11440 Trp53 transformation related protein 53 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0001412 excessive scratching IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:16751807 11440 Trp53 transformation related protein 53 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18451155 11440 Trp53 transformation related protein 53 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:11076674 11440 Trp53 transformation related protein 53 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:22964582 11440 Trp53 transformation related protein 53 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:10783170 11440 Trp53 transformation related protein 53 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:15821748 11440 Trp53 transformation related protein 53 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16751807 11440 Trp53 transformation related protein 53 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:19477430 11440 Trp53 transformation related protein 53 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17334357 11440 Trp53 transformation related protein 53 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:20362536 11440 Trp53 transformation related protein 53 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170615 MGI PMID:26411367 11440 Trp53 transformation related protein 53 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:22187431 11440 Trp53 transformation related protein 53 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:24332968 11440 Trp53 transformation related protein 53 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21674502 11440 Trp53 transformation related protein 53 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0001577 anemia IAGP N RGD:5509061 20180830 MGI PMID:29479066 11440 Trp53 transformation related protein 53 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17334357 11440 Trp53 transformation related protein 53 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14702042 11440 Trp53 transformation related protein 53 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15081359 11440 Trp53 transformation related protein 53 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16199867 11440 Trp53 transformation related protein 53 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16757976 11440 Trp53 transformation related protein 53 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20150129 MGI PMID:24706806 11440 Trp53 transformation related protein 53 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:19779492 11440 Trp53 transformation related protein 53 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20210506 MGI PMID:31794893 11440 Trp53 transformation related protein 53 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0001661 extended life span IAGP N RGD:5509061 20170831 MGI PMID:17533180 11440 Trp53 transformation related protein 53 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:15361844 11440 Trp53 transformation related protein 53 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17289567 11440 Trp53 transformation related protein 53 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20826531 11440 Trp53 transformation related protein 53 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20962274 11440 Trp53 transformation related protein 53 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20240620 MGI PMID:32628936 11440 Trp53 transformation related protein 53 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:17325035 11440 Trp53 transformation related protein 53 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10191063 11440 Trp53 transformation related protein 53 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11172041 11440 Trp53 transformation related protein 53 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11980714 11440 Trp53 transformation related protein 53 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12101245 11440 Trp53 transformation related protein 53 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12832489 11440 Trp53 transformation related protein 53 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16790550 11440 Trp53 transformation related protein 53 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17325035 11440 Trp53 transformation related protein 53 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21317535 11440 Trp53 transformation related protein 53 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22579044 11440 Trp53 transformation related protein 53 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9207798 11440 Trp53 transformation related protein 53 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9872327 11440 Trp53 transformation related protein 53 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20190328 MGI PMID:30232008 11440 Trp53 transformation related protein 53 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17325035 11440 Trp53 transformation related protein 53 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20150129 MGI PMID:24706806 11440 Trp53 transformation related protein 53 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:9207798 11440 Trp53 transformation related protein 53 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:20826531 11440 Trp53 transformation related protein 53 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:9207798 11440 Trp53 transformation related protein 53 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10191063 11440 Trp53 transformation related protein 53 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17000755 11440 Trp53 transformation related protein 53 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:20858271 11440 Trp53 transformation related protein 53 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10786799 11440 Trp53 transformation related protein 53 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18559481 11440 Trp53 transformation related protein 53 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20210617 MGI PMID:28747430 11440 Trp53 transformation related protein 53 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22213803 11440 Trp53 transformation related protein 53 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20348955 11440 Trp53 transformation related protein 53 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:12414647 11440 Trp53 transformation related protein 53 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20190711 MGI PMID:29635765 11440 Trp53 transformation related protein 53 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20190711 MGI PMID:29635765 11440 Trp53 transformation related protein 53 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:22964582 11440 Trp53 transformation related protein 53 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20190711 MGI PMID:29635765 11440 Trp53 transformation related protein 53 gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18304521 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11694875 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15131084 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15150107 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16715125 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17097565 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17510390 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20473325 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21324922 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22358843 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20150514 MGI PMID:24784840 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20160331 MGI PMID:25330770 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20160428 MGI PMID:16166291 11440 Trp53 transformation related protein 53 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20190523 MGI PMID:21282721 11440 Trp53 transformation related protein 53 gene MP:0001884 mammary gland alveolar hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17653086 11440 Trp53 transformation related protein 53 gene MP:0001885 mammary gland duct hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16715125 11440 Trp53 transformation related protein 53 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:9851974 11440 Trp53 transformation related protein 53 gene MP:0001914 hemorrhage IEA N RGD:5509061 20111116 MGI 11440 Trp53 transformation related protein 53 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20230622 MGI PMID:25671302 11440 Trp53 transformation related protein 53 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21124965 11440 Trp53 transformation related protein 53 gene MP:0001925 male infertility IAGP N RGD:5509061 20220224 MGI PMID:21277975 11440 Trp53 transformation related protein 53 gene MP:0001926 female infertility IAGP N RGD:5509061 20220224 MGI PMID:21277975 11440 Trp53 transformation related protein 53 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20170608 MGI PMID:24711431 11440 Trp53 transformation related protein 53 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10077642 11440 Trp53 transformation related protein 53 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12555066 11440 Trp53 transformation related protein 53 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16751807 11440 Trp53 transformation related protein 53 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22964582 11440 Trp53 transformation related protein 53 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20150924 MGI PMID:25035393 11440 Trp53 transformation related protein 53 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20230622 MGI PMID:25671302 11440 Trp53 transformation related protein 53 gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:17653086 11440 Trp53 transformation related protein 53 gene MP:0002013 increased pilomatricoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17097565 11440 Trp53 transformation related protein 53 gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:15894267 11440 Trp53 transformation related protein 53 gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:17486075 11440 Trp53 transformation related protein 53 gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:22574128 11440 Trp53 transformation related protein 53 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:23741457 11440 Trp53 transformation related protein 53 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20161222 MGI PMID:27354067 11440 Trp53 transformation related protein 53 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12414647 11440 Trp53 transformation related protein 53 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15652750 11440 Trp53 transformation related protein 53 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21056012 11440 Trp53 transformation related protein 53 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20180809 MGI PMID:11159909 11440 Trp53 transformation related protein 53 gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15314658 11440 Trp53 transformation related protein 53 gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16702401 11440 Trp53 transformation related protein 53 gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16757976 11440 Trp53 transformation related protein 53 gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17417627 11440 Trp53 transformation related protein 53 gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21674502 11440 Trp53 transformation related protein 53 gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22896338 11440 Trp53 transformation related protein 53 gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20201224 MGI PMID:31483066 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10077642 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10346812 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10591652 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10760284 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11169961 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11280729 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11323676 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11544182 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11694875 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12096340 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12414647 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12432262 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12914700 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14647411 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14702042 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15131084 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15150107 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:1552940 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15607980 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15821748 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16278673 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16616333 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16670198 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16702401 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16757976 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16767157 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16785989 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17158963 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17417627 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17486075 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17728759 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17906694 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18199537 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18559481 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18835033 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19251665 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19881536 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20473325 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21552324 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22358843 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22682249 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23474986 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23665223 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23754438 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24239359 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:7504233 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:7922305 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:7951317 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8048955 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20170314 MGI PMID:27815386 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20170831 MGI PMID:17533180 11440 Trp53 transformation related protein 53 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20220224 MGI PMID:21277975 11440 Trp53 transformation related protein 53 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:12914701 11440 Trp53 transformation related protein 53 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10786799 11440 Trp53 transformation related protein 53 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12914700 11440 Trp53 transformation related protein 53 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15343266 11440 Trp53 transformation related protein 53 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15607980 11440 Trp53 transformation related protein 53 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 11440 Trp53 transformation related protein 53 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17728759 11440 Trp53 transformation related protein 53 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18775323 11440 Trp53 transformation related protein 53 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21349429 11440 Trp53 transformation related protein 53 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21552324 11440 Trp53 transformation related protein 53 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22689981 11440 Trp53 transformation related protein 53 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20160225 MGI PMID:25144937 11440 Trp53 transformation related protein 53 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20160915 MGI PMID:23538418 11440 Trp53 transformation related protein 53 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20201224 MGI PMID:31483066 11440 Trp53 transformation related protein 53 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20230615 MGI PMID:23656786 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10077642 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10760284 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11323676 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12208847 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12555066 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12914700 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14647411 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14702042 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14706337 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15131084 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15607980 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15894267 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15924142 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16260620 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16473278 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16670198 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16751807 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17417627 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17984302 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18775323 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19126872 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19767771 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20215524 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20348955 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21324922 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21349429 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21368836 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21685933 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23665223 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7504233 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7922305 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9584189 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20160225 MGI PMID:25144937 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20160915 MGI PMID:23538418 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20170608 MGI PMID:23979016 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20180712 MGI PMID:29754823 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20180809 MGI PMID:22815056 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20180906 MGI PMID:25565005 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20201224 MGI PMID:31483066 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20211021 MGI PMID:28076792 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20230615 MGI PMID:23656786 11440 Trp53 transformation related protein 53 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20230622 MGI PMID:25671302 11440 Trp53 transformation related protein 53 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:17906694 11440 Trp53 transformation related protein 53 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 11440 Trp53 transformation related protein 53 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:19332766 11440 Trp53 transformation related protein 53 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20160915 MGI PMID:23538418 11440 Trp53 transformation related protein 53 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20180906 MGI PMID:25565005 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15607980 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16288016 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17299132 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19765830 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19847165 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21317887 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22228755 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22611036 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22964582 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23285300 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23565506 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20150910 MGI PMID:17676035 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20150924 MGI PMID:25035393 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:14522252 11440 Trp53 transformation related protein 53 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20171116 MGI PMID:11751631 11440 Trp53 transformation related protein 53 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591652 11440 Trp53 transformation related protein 53 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 11440 Trp53 transformation related protein 53 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16397217 11440 Trp53 transformation related protein 53 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18242513 11440 Trp53 transformation related protein 53 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591652 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10760284 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11169961 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12914700 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14647411 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14702042 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15343266 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:1552940 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15607981 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15652750 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15674344 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15821748 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16260620 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16357136 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16751807 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17417627 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17486075 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17676052 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18835033 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19477430 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19881536 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19956606 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21056012 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21512139 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21552324 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22228755 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22293175 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23166633 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23754438 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24115439 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24239359 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7922305 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7951317 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141127 MGI PMID:9861017 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20151008 MGI PMID:24292676 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20160428 MGI PMID:16166291 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20160915 MGI PMID:23412344 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20160915 MGI PMID:23538418 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20170608 MGI PMID:23979016 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20201224 MGI PMID:31483066 11440 Trp53 transformation related protein 53 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20230615 MGI PMID:23656786 11440 Trp53 transformation related protein 53 gene MP:0002033 increased malignant triton tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 11440 Trp53 transformation related protein 53 gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 11440 Trp53 transformation related protein 53 gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23665223 11440 Trp53 transformation related protein 53 gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7922305 11440 Trp53 transformation related protein 53 gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7951317 11440 Trp53 transformation related protein 53 gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20211021 MGI PMID:28076792 11440 Trp53 transformation related protein 53 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 11440 Trp53 transformation related protein 53 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14706339 11440 Trp53 transformation related protein 53 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15489287 11440 Trp53 transformation related protein 53 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16785989 11440 Trp53 transformation related protein 53 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17452975 11440 Trp53 transformation related protein 53 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 11440 Trp53 transformation related protein 53 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7922305 11440 Trp53 transformation related protein 53 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141127 MGI PMID:9861017 11440 Trp53 transformation related protein 53 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20211021 MGI PMID:28076792 11440 Trp53 transformation related protein 53 gene MP:0002037 increased fibrohistocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10760284 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15314658 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15607980 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15607981 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16079851 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17363841 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17486075 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17607363 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18835033 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19176372 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19261747 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20215524 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20676140 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21331045 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21502497 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21799785 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22574128 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23665223 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141127 MGI PMID:9861017 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20150319 MGI PMID:22617326 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:25815421 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20160915 MGI PMID:23538418 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20201224 MGI PMID:31483066 11440 Trp53 transformation related protein 53 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20230615 MGI PMID:23656786 11440 Trp53 transformation related protein 53 gene MP:0002039 increased neuroblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 11440 Trp53 transformation related protein 53 gene MP:0002039 increased neuroblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9214616 11440 Trp53 transformation related protein 53 gene MP:0002039 increased neuroblastoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 11440 Trp53 transformation related protein 53 gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16751807 11440 Trp53 transformation related protein 53 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16227443 11440 Trp53 transformation related protein 53 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24029233 11440 Trp53 transformation related protein 53 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20200820 MGI PMID:32728212 11440 Trp53 transformation related protein 53 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16288016 11440 Trp53 transformation related protein 53 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17486075 11440 Trp53 transformation related protein 53 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22411819 11440 Trp53 transformation related protein 53 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23285300 11440 Trp53 transformation related protein 53 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24239348 11440 Trp53 transformation related protein 53 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20151112 MGI PMID:22606359 11440 Trp53 transformation related protein 53 gene MP:0002049 increased extremity angiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:11323676 11440 Trp53 transformation related protein 53 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:15456863 11440 Trp53 transformation related protein 53 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14729946 11440 Trp53 transformation related protein 53 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15319471 11440 Trp53 transformation related protein 53 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15652750 11440 Trp53 transformation related protein 53 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16357136 11440 Trp53 transformation related protein 53 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16397217 11440 Trp53 transformation related protein 53 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16767157 11440 Trp53 transformation related protein 53 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 11440 Trp53 transformation related protein 53 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20473325 11440 Trp53 transformation related protein 53 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24209622 11440 Trp53 transformation related protein 53 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9584189 11440 Trp53 transformation related protein 53 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20151015 MGI PMID:25512531 11440 Trp53 transformation related protein 53 gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:19847165 11440 Trp53 transformation related protein 53 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:15674344 11440 Trp53 transformation related protein 53 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:18451155 11440 Trp53 transformation related protein 53 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:18948956 11440 Trp53 transformation related protein 53 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:19477430 11440 Trp53 transformation related protein 53 gene MP:0002064 seizures IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9171368 11440 Trp53 transformation related protein 53 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11076674 11440 Trp53 transformation related protein 53 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17936560 11440 Trp53 transformation related protein 53 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23047698 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10077642 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10591652 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10591653 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10757812 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10786799 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10911993 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11323676 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11544182 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11967151 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12208847 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12234974 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12555066 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12670909 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12914700 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12914701 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14706337 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15131084 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15343266 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:1552940 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15607980 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15607981 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15674344 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15894267 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16079851 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16227443 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16260620 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16278673 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16288016 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16357136 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16397237 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16670198 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16751807 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16777961 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17158963 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17349585 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17417627 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17452975 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17486075 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17728759 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17967868 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18328429 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18451155 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18559481 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18632614 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19126872 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19164512 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19176372 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19261747 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19477430 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19620979 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19633665 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19767771 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19881536 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20215524 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20348955 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20406986 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20697345 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20847051 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21056012 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21242963 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21324922 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21331045 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21368836 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21436583 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21625383 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21799785 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22232209 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22266220 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22341455 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22411819 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22611036 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22689981 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23166633 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23486187 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23665223 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23754438 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24115439 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7951317 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9584189 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20141225 MGI PMID:24652652 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20150326 MGI PMID:24979267 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20150507 MGI PMID:23851502 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20150514 MGI PMID:24784840 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20150910 MGI PMID:17676035 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20150924 MGI PMID:25035393 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20151015 MGI PMID:25512531 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20160107 MGI PMID:25119042 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20160204 MGI PMID:25815421 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20160225 MGI PMID:25144937 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20160324 MGI PMID:12426394 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20160428 MGI PMID:16166291 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20160915 MGI PMID:23412344 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20160915 MGI PMID:23538418 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20161013 MGI PMID:26659571 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20170601 MGI PMID:22190384 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20170608 MGI PMID:24711431 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20170615 MGI PMID:26411367 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20180809 MGI PMID:22815056 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20180830 MGI PMID:29479066 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20190131 MGI PMID:28934293 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20190516 MGI PMID:28790031 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20190711 MGI PMID:29635765 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20191205 MGI PMID:25453901 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20191205 MGI PMID:31685994 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20200423 MGI PMID:30858608 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20200806 MGI PMID:31677819 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20201224 MGI PMID:31483066 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20210225 MGI PMID:30952657 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20230601 MGI PMID:30093633 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20230608 MGI PMID:33594717 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20230615 MGI PMID:23656786 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20230615 MGI PMID:28655788 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20230615 MGI PMID:34803166 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20230622 MGI PMID:25671302 11440 Trp53 transformation related protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20241024 MGI PMID:31048544 11440 Trp53 transformation related protein 53 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11884603 11440 Trp53 transformation related protein 53 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15361844 11440 Trp53 transformation related protein 53 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9171368 11440 Trp53 transformation related protein 53 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9872327 11440 Trp53 transformation related protein 53 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11891301 11440 Trp53 transformation related protein 53 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:15231717 11440 Trp53 transformation related protein 53 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11076674 11440 Trp53 transformation related protein 53 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20150129 MGI PMID:24706806 11440 Trp53 transformation related protein 53 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17129780 11440 Trp53 transformation related protein 53 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20151015 MGI PMID:25512531 11440 Trp53 transformation related protein 53 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10783170 11440 Trp53 transformation related protein 53 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11694875 11440 Trp53 transformation related protein 53 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16354690 11440 Trp53 transformation related protein 53 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17289567 11440 Trp53 transformation related protein 53 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17998932 11440 Trp53 transformation related protein 53 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19556538 11440 Trp53 transformation related protein 53 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21730163 11440 Trp53 transformation related protein 53 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7477326 11440 Trp53 transformation related protein 53 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7477327 11440 Trp53 transformation related protein 53 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0002183 gliosis IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:22411819 11440 Trp53 transformation related protein 53 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:23166633 11440 Trp53 transformation related protein 53 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:23166633 11440 Trp53 transformation related protein 53 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20181227 MGI PMID:18641651 11440 Trp53 transformation related protein 53 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12509446 11440 Trp53 transformation related protein 53 gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20826531 11440 Trp53 transformation related protein 53 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10786799 11440 Trp53 transformation related protein 53 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20200820 MGI PMID:32728212 11440 Trp53 transformation related protein 53 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16473278 11440 Trp53 transformation related protein 53 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16473278 11440 Trp53 transformation related protein 53 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:12944479 11440 Trp53 transformation related protein 53 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:19966810 11440 Trp53 transformation related protein 53 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10346812 11440 Trp53 transformation related protein 53 gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11967151 11440 Trp53 transformation related protein 53 gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12914700 11440 Trp53 transformation related protein 53 gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16227443 11440 Trp53 transformation related protein 53 gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18835033 11440 Trp53 transformation related protein 53 gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23665223 11440 Trp53 transformation related protein 53 gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24115439 11440 Trp53 transformation related protein 53 gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7922305 11440 Trp53 transformation related protein 53 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20151015 MGI PMID:25512531 11440 Trp53 transformation related protein 53 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:19620979 11440 Trp53 transformation related protein 53 gene MP:0002639 micrognathia IAGP N RGD:5509061 20230309 MGI PMID:35593225 11440 Trp53 transformation related protein 53 gene MP:0002661 abnormal corpus epididymis morphology IAGP N RGD:5509061 20141204 MGI PMID:22678923 11440 Trp53 transformation related protein 53 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:20858271 11440 Trp53 transformation related protein 53 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21124965 11440 Trp53 transformation related protein 53 gene MP:0002700 increased opacity of vitreous body IAGP N RGD:5509061 20141003 MGI PMID:10393064 11440 Trp53 transformation related protein 53 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20151008 MGI PMID:24292676 11440 Trp53 transformation related protein 53 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:21831840 11440 Trp53 transformation related protein 53 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10393064 11440 Trp53 transformation related protein 53 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20230615 MGI PMID:23656786 11440 Trp53 transformation related protein 53 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10885750 11440 Trp53 transformation related protein 53 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:10393064 11440 Trp53 transformation related protein 53 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19966810 11440 Trp53 transformation related protein 53 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20180830 MGI PMID:29479066 11440 Trp53 transformation related protein 53 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20230622 MGI PMID:25671302 11440 Trp53 transformation related protein 53 gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20697345 11440 Trp53 transformation related protein 53 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:17510390 11440 Trp53 transformation related protein 53 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16227443 11440 Trp53 transformation related protein 53 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20150514 MGI PMID:24784840 11440 Trp53 transformation related protein 53 gene MP:0002989 small kidney IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0003010 decreased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12509446 11440 Trp53 transformation related protein 53 gene MP:0003010 decreased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0003010 decreased mortality induced by ionizing radiation IAGP N RGD:5509061 20151015 MGI PMID:25512531 11440 Trp53 transformation related protein 53 gene MP:0003046 liver cirrhosis IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0003051 curly tail IAGP N RGD:5509061 20180809 MGI PMID:22815056 11440 Trp53 transformation related protein 53 gene MP:0003054 spina bifida IAGP N RGD:5509061 20180809 MGI PMID:22815056 11440 Trp53 transformation related protein 53 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:10973245 11440 Trp53 transformation related protein 53 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:11076674 11440 Trp53 transformation related protein 53 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15607981 11440 Trp53 transformation related protein 53 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15654339 11440 Trp53 transformation related protein 53 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16006521 11440 Trp53 transformation related protein 53 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16616333 11440 Trp53 transformation related protein 53 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:17158931 11440 Trp53 transformation related protein 53 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18160036 11440 Trp53 transformation related protein 53 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18216268 11440 Trp53 transformation related protein 53 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:21127973 11440 Trp53 transformation related protein 53 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:22682249 11440 Trp53 transformation related protein 53 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:9472983 11440 Trp53 transformation related protein 53 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11076674 11440 Trp53 transformation related protein 53 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:21831840 11440 Trp53 transformation related protein 53 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:22579044 11440 Trp53 transformation related protein 53 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19966810 11440 Trp53 transformation related protein 53 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20180830 MGI PMID:29479066 11440 Trp53 transformation related protein 53 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20230622 MGI PMID:25671302 11440 Trp53 transformation related protein 53 gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22266795 11440 Trp53 transformation related protein 53 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10911993 11440 Trp53 transformation related protein 53 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11150333 11440 Trp53 transformation related protein 53 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16777961 11440 Trp53 transformation related protein 53 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:16757976 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:10973245 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:12097646 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:12192050 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:15343266 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:15607980 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:15607981 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:15924142 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:17158931 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:19779492 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:20194434 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:21565614 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:22682249 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:23665223 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20160915 MGI PMID:23538418 11440 Trp53 transformation related protein 53 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20220922 MGI PMID:27668660 11440 Trp53 transformation related protein 53 gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22044588 11440 Trp53 transformation related protein 53 gene MP:0003236 abnormal lens capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:11891301 11440 Trp53 transformation related protein 53 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17129780 11440 Trp53 transformation related protein 53 gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:16357136 11440 Trp53 transformation related protein 53 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:15894267 11440 Trp53 transformation related protein 53 gene MP:0003277 increased esophageal papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:15894267 11440 Trp53 transformation related protein 53 gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:16357136 11440 Trp53 transformation related protein 53 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20190711 MGI PMID:29635765 11440 Trp53 transformation related protein 53 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19234449 11440 Trp53 transformation related protein 53 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15607980 11440 Trp53 transformation related protein 53 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16278673 11440 Trp53 transformation related protein 53 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16397237 11440 Trp53 transformation related protein 53 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16751807 11440 Trp53 transformation related protein 53 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19234449 11440 Trp53 transformation related protein 53 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 11440 Trp53 transformation related protein 53 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24029233 11440 Trp53 transformation related protein 53 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20191205 MGI PMID:25453901 11440 Trp53 transformation related protein 53 gene MP:0003335 exocrine pancreatic insufficiency IAGP N RGD:5509061 20141003 MGI PMID:21056012 11440 Trp53 transformation related protein 53 gene MP:0003365 increased glucagonoma incidence IAGP N RGD:5509061 20151008 MGI PMID:24292676 11440 Trp53 transformation related protein 53 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:15314658 11440 Trp53 transformation related protein 53 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:19847165 11440 Trp53 transformation related protein 53 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22341455 11440 Trp53 transformation related protein 53 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20191205 MGI PMID:31685994 11440 Trp53 transformation related protein 53 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20230608 MGI PMID:33594717 11440 Trp53 transformation related protein 53 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:12096340 11440 Trp53 transformation related protein 53 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:17486075 11440 Trp53 transformation related protein 53 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:17607363 11440 Trp53 transformation related protein 53 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:18835033 11440 Trp53 transformation related protein 53 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:19164512 11440 Trp53 transformation related protein 53 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:19176372 11440 Trp53 transformation related protein 53 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:19847165 11440 Trp53 transformation related protein 53 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:20473325 11440 Trp53 transformation related protein 53 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:22172724 11440 Trp53 transformation related protein 53 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:23657012 11440 Trp53 transformation related protein 53 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:7922305 11440 Trp53 transformation related protein 53 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:7951317 11440 Trp53 transformation related protein 53 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20230601 MGI PMID:35700263 11440 Trp53 transformation related protein 53 gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20161222 MGI PMID:27354067 11440 Trp53 transformation related protein 53 gene MP:0003570 increased uterus leiomyoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 11440 Trp53 transformation related protein 53 gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20150319 MGI PMID:22617326 11440 Trp53 transformation related protein 53 gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12839925 11440 Trp53 transformation related protein 53 gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20150319 MGI PMID:22617326 11440 Trp53 transformation related protein 53 gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:25815421 11440 Trp53 transformation related protein 53 gene MP:0003587 ureter obstruction IAGP N RGD:5509061 20141003 MGI PMID:17653086 11440 Trp53 transformation related protein 53 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:16079851 11440 Trp53 transformation related protein 53 gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:20585617 11440 Trp53 transformation related protein 53 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:22266795 11440 Trp53 transformation related protein 53 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10077642 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10346812 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10760284 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11323676 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:1552940 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15607980 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16751807 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17486075 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20587514 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21552324 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23665223 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7922305 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141127 MGI PMID:9861017 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 11440 Trp53 transformation related protein 53 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20211021 MGI PMID:28076792 11440 Trp53 transformation related protein 53 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22044588 11440 Trp53 transformation related protein 53 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22682249 11440 Trp53 transformation related protein 53 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23665223 11440 Trp53 transformation related protein 53 gene MP:0003701 elevated level of mitotic sister chromatid exchange IAGP N RGD:5509061 20141003 MGI PMID:16839876 11440 Trp53 transformation related protein 53 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:12414647 11440 Trp53 transformation related protein 53 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:16839876 11440 Trp53 transformation related protein 53 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:20473325 11440 Trp53 transformation related protein 53 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:21368836 11440 Trp53 transformation related protein 53 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:22341455 11440 Trp53 transformation related protein 53 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:22579044 11440 Trp53 transformation related protein 53 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:15314658 11440 Trp53 transformation related protein 53 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20676140 11440 Trp53 transformation related protein 53 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20697345 11440 Trp53 transformation related protein 53 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21625383 11440 Trp53 transformation related protein 53 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22228755 11440 Trp53 transformation related protein 53 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22896338 11440 Trp53 transformation related protein 53 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20210506 MGI PMID:31794893 11440 Trp53 transformation related protein 53 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20230601 MGI PMID:30093633 11440 Trp53 transformation related protein 53 gene MP:0003750 increased mouth tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23657012 11440 Trp53 transformation related protein 53 gene MP:0003750 increased mouth tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24029233 11440 Trp53 transformation related protein 53 gene MP:0003751 oral leukoplakia IAGP N RGD:5509061 20141003 MGI PMID:19679647 11440 Trp53 transformation related protein 53 gene MP:0003751 oral leukoplakia IAGP N RGD:5509061 20141003 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:19881536 11440 Trp53 transformation related protein 53 gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:21127973 11440 Trp53 transformation related protein 53 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:19620979 11440 Trp53 transformation related protein 53 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10760284 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12414647 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:1552940 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16357136 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16546942 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17486075 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18559481 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20215524 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20587514 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21242963 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23486187 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7922305 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141127 MGI PMID:9861017 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20160804 MGI PMID:24141783 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20161013 MGI PMID:26659571 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:26360410 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:29743593 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:30093633 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:35700263 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:36073547 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230608 MGI PMID:33594717 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230615 MGI PMID:23656786 11440 Trp53 transformation related protein 53 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230615 MGI PMID:28655788 11440 Trp53 transformation related protein 53 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20150326 MGI PMID:24979267 11440 Trp53 transformation related protein 53 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:20826531 11440 Trp53 transformation related protein 53 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20210422 MGI PMID:32381628 11440 Trp53 transformation related protein 53 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20210422 MGI PMID:32381628 11440 Trp53 transformation related protein 53 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0003927 increased cellular glucose import IAGP N RGD:5509061 20141003 MGI PMID:22682249 11440 Trp53 transformation related protein 53 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15361844 11440 Trp53 transformation related protein 53 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17170753 11440 Trp53 transformation related protein 53 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17325035 11440 Trp53 transformation related protein 53 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20826531 11440 Trp53 transformation related protein 53 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20962274 11440 Trp53 transformation related protein 53 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21317535 11440 Trp53 transformation related protein 53 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22579044 11440 Trp53 transformation related protein 53 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9171368 11440 Trp53 transformation related protein 53 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9207798 11440 Trp53 transformation related protein 53 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20141003 MGI PMID:10508513 11440 Trp53 transformation related protein 53 gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20141003 MGI PMID:17251932 11440 Trp53 transformation related protein 53 gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20141003 MGI PMID:9872327 11440 Trp53 transformation related protein 53 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:14702042 11440 Trp53 transformation related protein 53 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:16767157 11440 Trp53 transformation related protein 53 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:20473325 11440 Trp53 transformation related protein 53 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:21368836 11440 Trp53 transformation related protein 53 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:21799785 11440 Trp53 transformation related protein 53 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20160225 MGI PMID:25144937 11440 Trp53 transformation related protein 53 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20190912 MGI PMID:31197172 11440 Trp53 transformation related protein 53 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20210211 MGI PMID:31662330 11440 Trp53 transformation related protein 53 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:11076674 11440 Trp53 transformation related protein 53 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:16715125 11440 Trp53 transformation related protein 53 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:16757976 11440 Trp53 transformation related protein 53 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:12832489 11440 Trp53 transformation related protein 53 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:16839876 11440 Trp53 transformation related protein 53 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:10881179 11440 Trp53 transformation related protein 53 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:17417627 11440 Trp53 transformation related protein 53 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:17713479 11440 Trp53 transformation related protein 53 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:19126872 11440 Trp53 transformation related protein 53 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:9872327 11440 Trp53 transformation related protein 53 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:10677503 11440 Trp53 transformation related protein 53 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:11431698 11440 Trp53 transformation related protein 53 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:12097646 11440 Trp53 transformation related protein 53 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:12101245 11440 Trp53 transformation related protein 53 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:12192050 11440 Trp53 transformation related protein 53 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:15654339 11440 Trp53 transformation related protein 53 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:17417627 11440 Trp53 transformation related protein 53 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:19881536 11440 Trp53 transformation related protein 53 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20150129 MGI PMID:24706806 11440 Trp53 transformation related protein 53 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20210204 MGI PMID:33110058 11440 Trp53 transformation related protein 53 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20240718 MGI PMID:34237032 11440 Trp53 transformation related protein 53 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:15181534 11440 Trp53 transformation related protein 53 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9207798 11440 Trp53 transformation related protein 53 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20180503 MGI PMID:29358667 11440 Trp53 transformation related protein 53 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10760284 11440 Trp53 transformation related protein 53 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15607980 11440 Trp53 transformation related protein 53 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17097565 11440 Trp53 transformation related protein 53 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17486075 11440 Trp53 transformation related protein 53 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17607363 11440 Trp53 transformation related protein 53 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19176372 11440 Trp53 transformation related protein 53 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20676140 11440 Trp53 transformation related protein 53 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141127 MGI PMID:9861017 11440 Trp53 transformation related protein 53 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20150514 MGI PMID:24784840 11440 Trp53 transformation related protein 53 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20211021 MGI PMID:28076792 11440 Trp53 transformation related protein 53 gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20150326 MGI PMID:24979267 11440 Trp53 transformation related protein 53 gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20180913 MGI PMID:24162662 11440 Trp53 transformation related protein 53 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:10911993 11440 Trp53 transformation related protein 53 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:16943427 11440 Trp53 transformation related protein 53 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17122775 11440 Trp53 transformation related protein 53 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17332334 11440 Trp53 transformation related protein 53 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17713479 11440 Trp53 transformation related protein 53 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:20587514 11440 Trp53 transformation related protein 53 gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:10514395 11440 Trp53 transformation related protein 53 gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12414647 11440 Trp53 transformation related protein 53 gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12909629 11440 Trp53 transformation related protein 53 gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:14729946 11440 Trp53 transformation related protein 53 gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17332334 11440 Trp53 transformation related protein 53 gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:20587514 11440 Trp53 transformation related protein 53 gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:21127973 11440 Trp53 transformation related protein 53 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20150129 MGI PMID:24706806 11440 Trp53 transformation related protein 53 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0004351 short humerus IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0004390 abnormal bronchoalveolar duct junction morphology IAGP N RGD:5509061 20141003 MGI PMID:22411819 11440 Trp53 transformation related protein 53 gene MP:0004478 increased testicular teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16227443 11440 Trp53 transformation related protein 53 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16651430 11440 Trp53 transformation related protein 53 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17363841 11440 Trp53 transformation related protein 53 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17607363 11440 Trp53 transformation related protein 53 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:21151170 11440 Trp53 transformation related protein 53 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20160428 MGI PMID:16166291 11440 Trp53 transformation related protein 53 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20181129 MGI PMID:30042151 11440 Trp53 transformation related protein 53 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:19779492 11440 Trp53 transformation related protein 53 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:20962274 11440 Trp53 transformation related protein 53 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:21317535 11440 Trp53 transformation related protein 53 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:22896338 11440 Trp53 transformation related protein 53 gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20150827 MGI PMID:20718941 11440 Trp53 transformation related protein 53 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:12566297 11440 Trp53 transformation related protein 53 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15314658 11440 Trp53 transformation related protein 53 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17607363 11440 Trp53 transformation related protein 53 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:16785989 11440 Trp53 transformation related protein 53 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:22940690 11440 Trp53 transformation related protein 53 gene MP:0004684 intervertebral disk degeneration IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:17996864 11440 Trp53 transformation related protein 53 gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:19620979 11440 Trp53 transformation related protein 53 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21844206 11440 Trp53 transformation related protein 53 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20160915 MGI PMID:23538418 11440 Trp53 transformation related protein 53 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20180830 MGI PMID:29479066 11440 Trp53 transformation related protein 53 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19966810 11440 Trp53 transformation related protein 53 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23230003 11440 Trp53 transformation related protein 53 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:17713479 11440 Trp53 transformation related protein 53 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22213803 11440 Trp53 transformation related protein 53 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21124965 11440 Trp53 transformation related protein 53 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220224 MGI PMID:21277975 11440 Trp53 transformation related protein 53 gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18632614 11440 Trp53 transformation related protein 53 gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141204 MGI PMID:22678923 11440 Trp53 transformation related protein 53 gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141204 MGI PMID:24930886 11440 Trp53 transformation related protein 53 gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141204 MGI PMID:22678923 11440 Trp53 transformation related protein 53 gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:18632614 11440 Trp53 transformation related protein 53 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20230622 MGI PMID:25671302 11440 Trp53 transformation related protein 53 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20230622 MGI PMID:25671302 11440 Trp53 transformation related protein 53 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10911993 11440 Trp53 transformation related protein 53 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20180712 MGI PMID:29754823 11440 Trp53 transformation related protein 53 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 11440 Trp53 transformation related protein 53 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16757976 11440 Trp53 transformation related protein 53 gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20170601 MGI PMID:22190384 11440 Trp53 transformation related protein 53 gene MP:0005135 increased thyroid-stimulating hormone level IAGP N RGD:5509061 20170608 MGI PMID:24711431 11440 Trp53 transformation related protein 53 gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20962274 11440 Trp53 transformation related protein 53 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:15894267 11440 Trp53 transformation related protein 53 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:19620979 11440 Trp53 transformation related protein 53 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:12642502 11440 Trp53 transformation related protein 53 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22232209 11440 Trp53 transformation related protein 53 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12642502 11440 Trp53 transformation related protein 53 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20170615 MGI PMID:26411367 11440 Trp53 transformation related protein 53 gene MP:0005195 abnormal posterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:10393064 11440 Trp53 transformation related protein 53 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0005202 lethargy IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:17363591 11440 Trp53 transformation related protein 53 gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:7478622 11440 Trp53 transformation related protein 53 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:19477430 11440 Trp53 transformation related protein 53 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0005299 abnormal eye posterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:17363591 11440 Trp53 transformation related protein 53 gene MP:0005323 dystonia IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0005324 ascites IAGP N RGD:5509061 20160204 MGI PMID:25815421 11440 Trp53 transformation related protein 53 gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20170601 MGI PMID:22190384 11440 Trp53 transformation related protein 53 gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:12432262 11440 Trp53 transformation related protein 53 gene MP:0005409 darkened coat color IAGP N RGD:5509061 20181227 MGI PMID:18641651 11440 Trp53 transformation related protein 53 gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:22266220 11440 Trp53 transformation related protein 53 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20180830 MGI PMID:29479066 11440 Trp53 transformation related protein 53 gene MP:0005488 bronchial epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7951317 11440 Trp53 transformation related protein 53 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11076674 11440 Trp53 transformation related protein 53 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:19570515 11440 Trp53 transformation related protein 53 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20150326 MGI PMID:24979267 11440 Trp53 transformation related protein 53 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20847051 11440 Trp53 transformation related protein 53 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22044588 11440 Trp53 transformation related protein 53 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17334357 11440 Trp53 transformation related protein 53 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10508513 11440 Trp53 transformation related protein 53 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16597604 11440 Trp53 transformation related protein 53 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16839876 11440 Trp53 transformation related protein 53 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17172844 11440 Trp53 transformation related protein 53 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21831840 11440 Trp53 transformation related protein 53 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22682249 11440 Trp53 transformation related protein 53 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23665223 11440 Trp53 transformation related protein 53 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23798389 11440 Trp53 transformation related protein 53 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20210204 MGI PMID:33110058 11440 Trp53 transformation related protein 53 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20210617 MGI PMID:28747430 11440 Trp53 transformation related protein 53 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20210617 MGI PMID:28747430 11440 Trp53 transformation related protein 53 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:22044588 11440 Trp53 transformation related protein 53 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10859164 11440 Trp53 transformation related protein 53 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21124965 11440 Trp53 transformation related protein 53 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21331045 11440 Trp53 transformation related protein 53 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20190912 MGI PMID:31197172 11440 Trp53 transformation related protein 53 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11150333 11440 Trp53 transformation related protein 53 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16227443 11440 Trp53 transformation related protein 53 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16616333 11440 Trp53 transformation related protein 53 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17158931 11440 Trp53 transformation related protein 53 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17332334 11440 Trp53 transformation related protein 53 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17417627 11440 Trp53 transformation related protein 53 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21565614 11440 Trp53 transformation related protein 53 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22358843 11440 Trp53 transformation related protein 53 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11076674 11440 Trp53 transformation related protein 53 gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0006206 embryonic lethality between somite formation and embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10567591 11440 Trp53 transformation related protein 53 gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20141003 MGI PMID:10393064 11440 Trp53 transformation related protein 53 gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10393064 11440 Trp53 transformation related protein 53 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20201224 MGI PMID:31483066 11440 Trp53 transformation related protein 53 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20190523 MGI PMID:21282721 11440 Trp53 transformation related protein 53 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:22940690 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10783170 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16260494 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16670198 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16751807 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17452975 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18775323 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19164512 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19213072 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19477430 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19633665 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22343890 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22574128 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22722829 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24115439 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141127 MGI PMID:9861017 11440 Trp53 transformation related protein 53 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20170314 MGI PMID:27815386 11440 Trp53 transformation related protein 53 gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20160915 MGI PMID:23538418 11440 Trp53 transformation related protein 53 gene MP:0006310 increased retinoblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17363591 11440 Trp53 transformation related protein 53 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:12642502 11440 Trp53 transformation related protein 53 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16757976 11440 Trp53 transformation related protein 53 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12839925 11440 Trp53 transformation related protein 53 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16278673 11440 Trp53 transformation related protein 53 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 11440 Trp53 transformation related protein 53 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20150319 MGI PMID:22617326 11440 Trp53 transformation related protein 53 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20161222 MGI PMID:27354067 11440 Trp53 transformation related protein 53 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:18216268 11440 Trp53 transformation related protein 53 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:19570515 11440 Trp53 transformation related protein 53 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21831840 11440 Trp53 transformation related protein 53 gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21127973 11440 Trp53 transformation related protein 53 gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:22228755 11440 Trp53 transformation related protein 53 gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:22682249 11440 Trp53 transformation related protein 53 gene MP:0008010 increased gastric adenocarcinoma incidence IAGP N RGD:5509061 20150514 MGI PMID:24784840 11440 Trp53 transformation related protein 53 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16288016 11440 Trp53 transformation related protein 53 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17299132 11440 Trp53 transformation related protein 53 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19765830 11440 Trp53 transformation related protein 53 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20406986 11440 Trp53 transformation related protein 53 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20676140 11440 Trp53 transformation related protein 53 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21317887 11440 Trp53 transformation related protein 53 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 11440 Trp53 transformation related protein 53 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22964582 11440 Trp53 transformation related protein 53 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20150910 MGI PMID:17676035 11440 Trp53 transformation related protein 53 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20150924 MGI PMID:25035393 11440 Trp53 transformation related protein 53 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20160428 MGI PMID:16166291 11440 Trp53 transformation related protein 53 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20171116 MGI PMID:11751631 11440 Trp53 transformation related protein 53 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16278673 11440 Trp53 transformation related protein 53 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20962274 11440 Trp53 transformation related protein 53 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 11440 Trp53 transformation related protein 53 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24029233 11440 Trp53 transformation related protein 53 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24120138 11440 Trp53 transformation related protein 53 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:23207905 11440 Trp53 transformation related protein 53 gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20141003 MGI PMID:19620979 11440 Trp53 transformation related protein 53 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:19779492 11440 Trp53 transformation related protein 53 gene MP:0008203 absent B-1a cells IAGP N RGD:5509061 20141003 MGI PMID:22213803 11440 Trp53 transformation related protein 53 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20151001 MGI PMID:25201955 11440 Trp53 transformation related protein 53 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 11440 Trp53 transformation related protein 53 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:22044588 11440 Trp53 transformation related protein 53 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12642502 11440 Trp53 transformation related protein 53 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20230309 MGI PMID:35593225 11440 Trp53 transformation related protein 53 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0008402 increased cellular sensitivity to alkylating agents IAGP N RGD:5509061 20141003 MGI PMID:22579044 11440 Trp53 transformation related protein 53 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:20587514 11440 Trp53 transformation related protein 53 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:12101245 11440 Trp53 transformation related protein 53 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:12909629 11440 Trp53 transformation related protein 53 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:12952892 11440 Trp53 transformation related protein 53 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:15456863 11440 Trp53 transformation related protein 53 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:15654339 11440 Trp53 transformation related protein 53 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:16537918 11440 Trp53 transformation related protein 53 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:17510390 11440 Trp53 transformation related protein 53 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:18216268 11440 Trp53 transformation related protein 53 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:20587514 11440 Trp53 transformation related protein 53 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:21127973 11440 Trp53 transformation related protein 53 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:21487039 11440 Trp53 transformation related protein 53 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20240718 MGI PMID:34237032 11440 Trp53 transformation related protein 53 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20210617 MGI PMID:28747430 11440 Trp53 transformation related protein 53 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20151015 MGI PMID:25512531 11440 Trp53 transformation related protein 53 gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22213803 11440 Trp53 transformation related protein 53 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15231717 11440 Trp53 transformation related protein 53 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20240718 MGI PMID:34237032 11440 Trp53 transformation related protein 53 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20210617 MGI PMID:33753942 11440 Trp53 transformation related protein 53 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0008623 increased circulating interleukin-3 level IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0008626 increased circulating interleukin-5 level IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20170615 MGI PMID:26411367 11440 Trp53 transformation related protein 53 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 11440 Trp53 transformation related protein 53 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:14522252 11440 Trp53 transformation related protein 53 gene MP:0008715 increased lung small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19765830 11440 Trp53 transformation related protein 53 gene MP:0008715 increased lung small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20406986 11440 Trp53 transformation related protein 53 gene MP:0008715 increased lung small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22611036 11440 Trp53 transformation related protein 53 gene MP:0008715 increased lung small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23047698 11440 Trp53 transformation related protein 53 gene MP:0008715 increased lung small cell carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:14522252 11440 Trp53 transformation related protein 53 gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22611036 11440 Trp53 transformation related protein 53 gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22964582 11440 Trp53 transformation related protein 53 gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:23207905 11440 Trp53 transformation related protein 53 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:21966279 11440 Trp53 transformation related protein 53 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:16546942 11440 Trp53 transformation related protein 53 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18835033 11440 Trp53 transformation related protein 53 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19126872 11440 Trp53 transformation related protein 53 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0008780 increased pancreatic acinar cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0008780 increased pancreatic acinar cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16169464 11440 Trp53 transformation related protein 53 gene MP:0008780 increased pancreatic acinar cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21056012 11440 Trp53 transformation related protein 53 gene MP:0008780 increased pancreatic acinar cell carcinoma incidence IAGP N RGD:5509061 20150326 MGI PMID:7478622 11440 Trp53 transformation related protein 53 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0008830 abnormal nucleolus morphology IAGP N RGD:5509061 20220324 MGI PMID:35139074 11440 Trp53 transformation related protein 53 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:10881179 11440 Trp53 transformation related protein 53 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:15894267 11440 Trp53 transformation related protein 53 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:19881536 11440 Trp53 transformation related protein 53 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:20676140 11440 Trp53 transformation related protein 53 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:22579044 11440 Trp53 transformation related protein 53 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:23754438 11440 Trp53 transformation related protein 53 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20160225 MGI PMID:25144937 11440 Trp53 transformation related protein 53 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20190328 MGI PMID:30232008 11440 Trp53 transformation related protein 53 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21331045 11440 Trp53 transformation related protein 53 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20200820 MGI PMID:32728212 11440 Trp53 transformation related protein 53 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0008891 decreased hepatocyte apoptosis IAGP N RGD:5509061 20191205 MGI PMID:25453901 11440 Trp53 transformation related protein 53 gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:21674502 11440 Trp53 transformation related protein 53 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:12952892 11440 Trp53 transformation related protein 53 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:19779492 11440 Trp53 transformation related protein 53 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:10508513 11440 Trp53 transformation related protein 53 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:12097646 11440 Trp53 transformation related protein 53 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:17158931 11440 Trp53 transformation related protein 53 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19966810 11440 Trp53 transformation related protein 53 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:19620979 11440 Trp53 transformation related protein 53 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20220224 MGI PMID:21277975 11440 Trp53 transformation related protein 53 gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20150326 MGI PMID:24979267 11440 Trp53 transformation related protein 53 gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18632614 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15894267 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16169464 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16585505 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17349585 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21056012 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22232209 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23453624 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20150528 MGI PMID:25878147 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20150827 MGI PMID:22541435 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20180809 MGI PMID:11159909 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20190131 MGI PMID:28934293 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20190516 MGI PMID:28790031 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20191205 MGI PMID:31685994 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200423 MGI PMID:30858608 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20210225 MGI PMID:30952657 11440 Trp53 transformation related protein 53 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20241024 MGI PMID:31048544 11440 Trp53 transformation related protein 53 gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:15894267 11440 Trp53 transformation related protein 53 gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22232209 11440 Trp53 transformation related protein 53 gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20190131 MGI PMID:28934293 11440 Trp53 transformation related protein 53 gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20190516 MGI PMID:28790031 11440 Trp53 transformation related protein 53 gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20191205 MGI PMID:31685994 11440 Trp53 transformation related protein 53 gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20241024 MGI PMID:31048544 11440 Trp53 transformation related protein 53 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16585505 11440 Trp53 transformation related protein 53 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20170615 MGI PMID:26411367 11440 Trp53 transformation related protein 53 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20180809 MGI PMID:11159909 11440 Trp53 transformation related protein 53 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20241024 MGI PMID:31048544 11440 Trp53 transformation related protein 53 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:20585617 11440 Trp53 transformation related protein 53 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22341455 11440 Trp53 transformation related protein 53 gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22341455 11440 Trp53 transformation related protein 53 gene MP:0009258 abnormal thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12909629 11440 Trp53 transformation related protein 53 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10973261 11440 Trp53 transformation related protein 53 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15652750 11440 Trp53 transformation related protein 53 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18451155 11440 Trp53 transformation related protein 53 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20170314 MGI PMID:27815386 11440 Trp53 transformation related protein 53 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21799785 11440 Trp53 transformation related protein 53 gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16288016 11440 Trp53 transformation related protein 53 gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22411819 11440 Trp53 transformation related protein 53 gene MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0009311 increased duodenum adenocarcinoma incidence IAGP N RGD:5509061 20150514 MGI PMID:24784840 11440 Trp53 transformation related protein 53 gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12914700 11440 Trp53 transformation related protein 53 gene MP:0009317 increased follicular lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19779492 11440 Trp53 transformation related protein 53 gene MP:0009318 increased splenic marginal zone lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23166633 11440 Trp53 transformation related protein 53 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 11440 Trp53 transformation related protein 53 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20211021 MGI PMID:28076792 11440 Trp53 transformation related protein 53 gene MP:0009332 abnormal splenocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21799785 11440 Trp53 transformation related protein 53 gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21799785 11440 Trp53 transformation related protein 53 gene MP:0009341 decreased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23166633 11440 Trp53 transformation related protein 53 gene MP:0009442 increased ovarian teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23741457 11440 Trp53 transformation related protein 53 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20190523 MGI PMID:21282721 11440 Trp53 transformation related protein 53 gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16715125 11440 Trp53 transformation related protein 53 gene MP:0009505 abnormal mammary gland lobule morphology IAGP N RGD:5509061 20190523 MGI PMID:21282721 11440 Trp53 transformation related protein 53 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:20473325 11440 Trp53 transformation related protein 53 gene MP:0009508 increased mammary gland ductal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17212342 11440 Trp53 transformation related protein 53 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17172844 11440 Trp53 transformation related protein 53 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10677503 11440 Trp53 transformation related protein 53 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19881536 11440 Trp53 transformation related protein 53 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20194434 11440 Trp53 transformation related protein 53 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20362536 11440 Trp53 transformation related protein 53 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21317535 11440 Trp53 transformation related protein 53 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22682249 11440 Trp53 transformation related protein 53 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23166633 11440 Trp53 transformation related protein 53 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23207905 11440 Trp53 transformation related protein 53 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23665223 11440 Trp53 transformation related protein 53 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20160324 MGI PMID:12426394 11440 Trp53 transformation related protein 53 gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19261747 11440 Trp53 transformation related protein 53 gene MP:0009551 increased urinary bladder transitional cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 11440 Trp53 transformation related protein 53 gene MP:0009552 urinary bladder obstruction IAGP N RGD:5509061 20141003 MGI PMID:16079851 11440 Trp53 transformation related protein 53 gene MP:0009566 meiotic nondisjunction IAGP N RGD:5509061 20141003 MGI PMID:12642502 11440 Trp53 transformation related protein 53 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19176372 11440 Trp53 transformation related protein 53 gene MP:0009591 increased liver adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0009591 increased liver adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0009600 hypergranulosis IAGP N RGD:5509061 20150326 MGI PMID:24979267 11440 Trp53 transformation related protein 53 gene MP:0009625 abnormal abdominal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20230824 MGI PMID:34257081 11440 Trp53 transformation related protein 53 gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19679647 11440 Trp53 transformation related protein 53 gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21502497 11440 Trp53 transformation related protein 53 gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20150326 MGI PMID:24979267 11440 Trp53 transformation related protein 53 gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20180913 MGI PMID:24162662 11440 Trp53 transformation related protein 53 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16533502 11440 Trp53 transformation related protein 53 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17363841 11440 Trp53 transformation related protein 53 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:20858271 11440 Trp53 transformation related protein 53 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:15150107 11440 Trp53 transformation related protein 53 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:16616333 11440 Trp53 transformation related protein 53 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:16757976 11440 Trp53 transformation related protein 53 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:21674502 11440 Trp53 transformation related protein 53 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22034435 11440 Trp53 transformation related protein 53 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22172724 11440 Trp53 transformation related protein 53 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20230615 MGI PMID:28655788 11440 Trp53 transformation related protein 53 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16260494 11440 Trp53 transformation related protein 53 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19633665 11440 Trp53 transformation related protein 53 gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:22266795 11440 Trp53 transformation related protein 53 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12533509 11440 Trp53 transformation related protein 53 gene MP:0010091 decreased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 11440 Trp53 transformation related protein 53 gene MP:0010094 abnormal chromosome stability IAGP N RGD:5509061 20141003 MGI PMID:23754438 11440 Trp53 transformation related protein 53 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:17097565 11440 Trp53 transformation related protein 53 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:20473325 11440 Trp53 transformation related protein 53 gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20200820 MGI PMID:32728212 11440 Trp53 transformation related protein 53 gene MP:0010173 increased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17653086 11440 Trp53 transformation related protein 53 gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20141003 MGI PMID:24115439 11440 Trp53 transformation related protein 53 gene MP:0010249 lactation failure IAGP N RGD:5509061 20190523 MGI PMID:21282721 11440 Trp53 transformation related protein 53 gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20587514 11440 Trp53 transformation related protein 53 gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21674502 11440 Trp53 transformation related protein 53 gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21685933 11440 Trp53 transformation related protein 53 gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20170608 MGI PMID:23979016 11440 Trp53 transformation related protein 53 gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22172724 11440 Trp53 transformation related protein 53 gene MP:0010273 increased classified tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22358843 11440 Trp53 transformation related protein 53 gene MP:0010274 increased organ/body region tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21565614 11440 Trp53 transformation related protein 53 gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20697345 11440 Trp53 transformation related protein 53 gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10973261 11440 Trp53 transformation related protein 53 gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15319471 11440 Trp53 transformation related protein 53 gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18451155 11440 Trp53 transformation related protein 53 gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18948956 11440 Trp53 transformation related protein 53 gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23887970 11440 Trp53 transformation related protein 53 gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20160922 MGI PMID:26704996 11440 Trp53 transformation related protein 53 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:12670909 11440 Trp53 transformation related protein 53 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:18948956 11440 Trp53 transformation related protein 53 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:19477430 11440 Trp53 transformation related protein 53 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:23887970 11440 Trp53 transformation related protein 53 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:9851974 11440 Trp53 transformation related protein 53 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 11440 Trp53 transformation related protein 53 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20160505 MGI PMID:26282165 11440 Trp53 transformation related protein 53 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20160922 MGI PMID:26704996 11440 Trp53 transformation related protein 53 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20170314 MGI PMID:27815386 11440 Trp53 transformation related protein 53 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 11440 Trp53 transformation related protein 53 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20160512 MGI PMID:21502497 11440 Trp53 transformation related protein 53 gene MP:0010280 increased skeletal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0010281 increased nervous system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0010281 increased nervous system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21242963 11440 Trp53 transformation related protein 53 gene MP:0010281 increased nervous system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23887970 11440 Trp53 transformation related protein 53 gene MP:0010285 decreased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22172724 11440 Trp53 transformation related protein 53 gene MP:0010287 increased reproductive system tumor incidence IAGP N RGD:5509061 20160915 MGI PMID:23538418 11440 Trp53 transformation related protein 53 gene MP:0010289 increased urinary system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21151170 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10319859 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11431698 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11694875 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15150107 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16546942 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17212342 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17525270 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17626182 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17653086 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20215524 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20473325 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20676140 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21324922 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22172724 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23657012 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24120138 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20160331 MGI PMID:25330770 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20160428 MGI PMID:16166291 11440 Trp53 transformation related protein 53 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20190523 MGI PMID:21282721 11440 Trp53 transformation related protein 53 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11694875 11440 Trp53 transformation related protein 53 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15456863 11440 Trp53 transformation related protein 53 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 11440 Trp53 transformation related protein 53 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17097565 11440 Trp53 transformation related protein 53 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17510390 11440 Trp53 transformation related protein 53 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17626182 11440 Trp53 transformation related protein 53 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21502497 11440 Trp53 transformation related protein 53 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22172724 11440 Trp53 transformation related protein 53 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23657012 11440 Trp53 transformation related protein 53 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20150326 MGI PMID:24979267 11440 Trp53 transformation related protein 53 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20180913 MGI PMID:24162662 11440 Trp53 transformation related protein 53 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16546942 11440 Trp53 transformation related protein 53 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16751807 11440 Trp53 transformation related protein 53 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24029233 11440 Trp53 transformation related protein 53 gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16278673 11440 Trp53 transformation related protein 53 gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16357136 11440 Trp53 transformation related protein 53 gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22266220 11440 Trp53 transformation related protein 53 gene MP:0010307 abnormal tumor latency IAGP N RGD:5509061 20141003 MGI PMID:16702401 11440 Trp53 transformation related protein 53 gene MP:0010307 abnormal tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22358843 11440 Trp53 transformation related protein 53 gene MP:0010307 abnormal tumor latency IAGP N RGD:5509061 20210506 MGI PMID:31794893 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:11280729 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:11694875 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:11967151 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:14744934 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:16023597 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:16767157 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:19477430 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22034435 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22172724 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:23657012 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:24115439 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20151015 MGI PMID:25512531 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20160915 MGI PMID:23538418 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20180712 MGI PMID:29754823 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20210506 MGI PMID:31794893 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20211021 MGI PMID:28076792 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20230601 MGI PMID:30093633 11440 Trp53 transformation related protein 53 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20230601 MGI PMID:36073547 11440 Trp53 transformation related protein 53 gene MP:0010309 increased mesothelioma incidence IAGP N RGD:5509061 20141003 MGI PMID:17486075 11440 Trp53 transformation related protein 53 gene MP:0010309 increased mesothelioma incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 11440 Trp53 transformation related protein 53 gene MP:0010309 increased mesothelioma incidence IAGP N RGD:5509061 20150507 MGI PMID:23851502 11440 Trp53 transformation related protein 53 gene MP:0010310 increased Schwannoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0010310 increased Schwannoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 11440 Trp53 transformation related protein 53 gene MP:0010312 increased oligodendroglioma incidence IAGP N RGD:5509061 20141003 MGI PMID:12670909 11440 Trp53 transformation related protein 53 gene MP:0010312 increased oligodendroglioma incidence IAGP N RGD:5509061 20141003 MGI PMID:23887970 11440 Trp53 transformation related protein 53 gene MP:0010312 increased oligodendroglioma incidence IAGP N RGD:5509061 20160505 MGI PMID:26282165 11440 Trp53 transformation related protein 53 gene MP:0010312 increased oligodendroglioma incidence IAGP N RGD:5509061 20160922 MGI PMID:26704996 11440 Trp53 transformation related protein 53 gene MP:0010313 increased osteoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0010314 increased neurofibroma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22266220 11440 Trp53 transformation related protein 53 gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23047698 11440 Trp53 transformation related protein 53 gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:7951317 11440 Trp53 transformation related protein 53 gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20160811 MGI PMID:26359368 11440 Trp53 transformation related protein 53 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15231717 11440 Trp53 transformation related protein 53 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22574128 11440 Trp53 transformation related protein 53 gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20150827 MGI PMID:20718941 11440 Trp53 transformation related protein 53 gene MP:0010334 pleural effusion IAGP N RGD:5509061 20141003 MGI PMID:18328429 11440 Trp53 transformation related protein 53 gene MP:0010337 increased chronic lymphocytic leukemia incidence IAGP N RGD:5509061 20160707 MGI PMID:19332766 11440 Trp53 transformation related protein 53 gene MP:0010343 increased lipoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0010343 increased lipoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0010344 increased hibernoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0010344 increased hibernoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23486187 11440 Trp53 transformation related protein 53 gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19765830 11440 Trp53 transformation related protein 53 gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:14522252 11440 Trp53 transformation related protein 53 gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20170601 MGI PMID:22190384 11440 Trp53 transformation related protein 53 gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20170608 MGI PMID:24711431 11440 Trp53 transformation related protein 53 gene MP:0010347 osseous metaplasia IAGP N RGD:5509061 20141003 MGI PMID:15221010 11440 Trp53 transformation related protein 53 gene MP:0010348 increased pancreatic islet cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7951317 11440 Trp53 transformation related protein 53 gene MP:0010348 increased pancreatic islet cell carcinoma incidence IAGP N RGD:5509061 20151008 MGI PMID:24292676 11440 Trp53 transformation related protein 53 gene MP:0010349 increased teratocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15894267 11440 Trp53 transformation related protein 53 gene MP:0010351 increased pituitary melanotroph tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:7951317 11440 Trp53 transformation related protein 53 gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16079851 11440 Trp53 transformation related protein 53 gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10760284 11440 Trp53 transformation related protein 53 gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11323676 11440 Trp53 transformation related protein 53 gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17486075 11440 Trp53 transformation related protein 53 gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19779492 11440 Trp53 transformation related protein 53 gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7922305 11440 Trp53 transformation related protein 53 gene MP:0010367 increased spindle cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17607363 11440 Trp53 transformation related protein 53 gene MP:0010367 increased spindle cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20697345 11440 Trp53 transformation related protein 53 gene MP:0010367 increased spindle cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0010367 increased spindle cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22358843 11440 Trp53 transformation related protein 53 gene MP:0010367 increased spindle cell carcinoma incidence IAGP N RGD:5509061 20160331 MGI PMID:25330770 11440 Trp53 transformation related protein 53 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0010537 tumor regression IAGP N RGD:5509061 20141003 MGI PMID:17251932 11440 Trp53 transformation related protein 53 gene MP:0010537 tumor regression IAGP N RGD:5509061 20141003 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0010537 tumor regression IAGP N RGD:5509061 20200423 MGI PMID:25208064 11440 Trp53 transformation related protein 53 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20141003 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20141003 MGI PMID:21799785 11440 Trp53 transformation related protein 53 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20141003 MGI PMID:22172724 11440 Trp53 transformation related protein 53 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20141003 MGI PMID:23845441 11440 Trp53 transformation related protein 53 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20160204 MGI PMID:14522252 11440 Trp53 transformation related protein 53 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20230601 MGI PMID:26360410 11440 Trp53 transformation related protein 53 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20230608 MGI PMID:33594717 11440 Trp53 transformation related protein 53 gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:11891301 11440 Trp53 transformation related protein 53 gene MP:0010715 retina coloboma IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0010727 increased glioblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10973261 11440 Trp53 transformation related protein 53 gene MP:0010727 increased glioblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18948956 11440 Trp53 transformation related protein 53 gene MP:0010727 increased glioblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21625383 11440 Trp53 transformation related protein 53 gene MP:0010727 increased glioblastoma incidence IAGP N RGD:5509061 20200806 MGI PMID:31677819 11440 Trp53 transformation related protein 53 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21724834 11440 Trp53 transformation related protein 53 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23230003 11440 Trp53 transformation related protein 53 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20180215 MGI PMID:28294115 11440 Trp53 transformation related protein 53 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20180503 MGI PMID:29358667 11440 Trp53 transformation related protein 53 gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:23285300 11440 Trp53 transformation related protein 53 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20181129 MGI PMID:30042151 11440 Trp53 transformation related protein 53 gene MP:0010918 abnormal pulmonary neuroendocrine body morphology IAGP N RGD:5509061 20141003 MGI PMID:23047698 11440 Trp53 transformation related protein 53 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18835033 11440 Trp53 transformation related protein 53 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22940690 11440 Trp53 transformation related protein 53 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:31197172 11440 Trp53 transformation related protein 53 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20230824 MGI PMID:34257081 11440 Trp53 transformation related protein 53 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10591653 11440 Trp53 transformation related protein 53 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24332968 11440 Trp53 transformation related protein 53 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14744934 11440 Trp53 transformation related protein 53 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17129780 11440 Trp53 transformation related protein 53 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21350561 11440 Trp53 transformation related protein 53 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20230309 MGI PMID:35593225 11440 Trp53 transformation related protein 53 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16777961 11440 Trp53 transformation related protein 53 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18835033 11440 Trp53 transformation related protein 53 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21549111 11440 Trp53 transformation related protein 53 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12588846 11440 Trp53 transformation related protein 53 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12944479 11440 Trp53 transformation related protein 53 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14729946 11440 Trp53 transformation related protein 53 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15607981 11440 Trp53 transformation related protein 53 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16616333 11440 Trp53 transformation related protein 53 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18216268 11440 Trp53 transformation related protein 53 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20671749 11440 Trp53 transformation related protein 53 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21317535 11440 Trp53 transformation related protein 53 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:30858352 11440 Trp53 transformation related protein 53 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240620 MGI PMID:38453366 11440 Trp53 transformation related protein 53 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10191063 11440 Trp53 transformation related protein 53 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11172041 11440 Trp53 transformation related protein 53 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15282321 11440 Trp53 transformation related protein 53 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16007073 11440 Trp53 transformation related protein 53 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17172844 11440 Trp53 transformation related protein 53 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18337066 11440 Trp53 transformation related protein 53 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20826531 11440 Trp53 transformation related protein 53 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21674502 11440 Trp53 transformation related protein 53 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20190328 MGI PMID:30232008 11440 Trp53 transformation related protein 53 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20190418 MGI PMID:27528230 11440 Trp53 transformation related protein 53 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10859164 11440 Trp53 transformation related protein 53 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17906694 11440 Trp53 transformation related protein 53 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29262616 11440 Trp53 transformation related protein 53 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11980714 11440 Trp53 transformation related protein 53 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15361844 11440 Trp53 transformation related protein 53 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8943369 11440 Trp53 transformation related protein 53 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11884603 11440 Trp53 transformation related protein 53 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12832489 11440 Trp53 transformation related protein 53 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15654339 11440 Trp53 transformation related protein 53 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16199867 11440 Trp53 transformation related protein 53 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16702401 11440 Trp53 transformation related protein 53 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16790550 11440 Trp53 transformation related protein 53 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17000755 11440 Trp53 transformation related protein 53 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17170753 11440 Trp53 transformation related protein 53 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24209622 11440 Trp53 transformation related protein 53 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9207798 11440 Trp53 transformation related protein 53 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9872327 11440 Trp53 transformation related protein 53 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20240718 MGI PMID:34237032 11440 Trp53 transformation related protein 53 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16007073 11440 Trp53 transformation related protein 53 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20160310 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12101245 11440 Trp53 transformation related protein 53 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15361844 11440 Trp53 transformation related protein 53 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19340312 11440 Trp53 transformation related protein 53 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20818388 11440 Trp53 transformation related protein 53 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20826531 11440 Trp53 transformation related protein 53 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20975950 11440 Trp53 transformation related protein 53 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20170608 MGI PMID:23979016 11440 Trp53 transformation related protein 53 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20220721 MGI PMID:34601382 11440 Trp53 transformation related protein 53 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20240808 MGI PMID:37306301 11440 Trp53 transformation related protein 53 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10911993 11440 Trp53 transformation related protein 53 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12588846 11440 Trp53 transformation related protein 53 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15081359 11440 Trp53 transformation related protein 53 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15181534 11440 Trp53 transformation related protein 53 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15607980 11440 Trp53 transformation related protein 53 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16702401 11440 Trp53 transformation related protein 53 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19620979 11440 Trp53 transformation related protein 53 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20180712 MGI PMID:29754823 11440 Trp53 transformation related protein 53 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20230615 MGI PMID:23656786 11440 Trp53 transformation related protein 53 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18835033 11440 Trp53 transformation related protein 53 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20170608 MGI PMID:23979016 11440 Trp53 transformation related protein 53 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14744934 11440 Trp53 transformation related protein 53 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17325035 11440 Trp53 transformation related protein 53 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17470788 11440 Trp53 transformation related protein 53 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20962274 11440 Trp53 transformation related protein 53 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21127973 11440 Trp53 transformation related protein 53 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20220721 MGI PMID:34601382 11440 Trp53 transformation related protein 53 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18835033 11440 Trp53 transformation related protein 53 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21127973 11440 Trp53 transformation related protein 53 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17289567 11440 Trp53 transformation related protein 53 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7922305 11440 Trp53 transformation related protein 53 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180809 MGI PMID:22815056 11440 Trp53 transformation related protein 53 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20190328 MGI PMID:30232008 11440 Trp53 transformation related protein 53 gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 11440 Trp53 transformation related protein 53 gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 11440 Trp53 transformation related protein 53 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21502497 11440 Trp53 transformation related protein 53 gene MP:0011638 abnormal mitochondrial chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:22044588 11440 Trp53 transformation related protein 53 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:16199867 11440 Trp53 transformation related protein 53 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:21127973 11440 Trp53 transformation related protein 53 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22682249 11440 Trp53 transformation related protein 53 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150212 MGI PMID:10508513 11440 Trp53 transformation related protein 53 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:10911993 11440 Trp53 transformation related protein 53 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:10973245 11440 Trp53 transformation related protein 53 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:11431698 11440 Trp53 transformation related protein 53 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:12101245 11440 Trp53 transformation related protein 53 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:15607980 11440 Trp53 transformation related protein 53 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:15607981 11440 Trp53 transformation related protein 53 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:16007073 11440 Trp53 transformation related protein 53 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:16023597 11440 Trp53 transformation related protein 53 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20151112 MGI PMID:22606359 11440 Trp53 transformation related protein 53 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20190711 MGI PMID:29635765 11440 Trp53 transformation related protein 53 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:16616333 11440 Trp53 transformation related protein 53 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:23798389 11440 Trp53 transformation related protein 53 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20240718 MGI PMID:34237032 11440 Trp53 transformation related protein 53 gene MP:0011804 increased cell migration IAGP N RGD:5509061 20161013 MGI PMID:26659571 11440 Trp53 transformation related protein 53 gene MP:0011903 decreased hematopoietic stem cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0012043 increased myoepithelioma incidence IAGP N RGD:5509061 20160331 MGI PMID:25330770 11440 Trp53 transformation related protein 53 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20210128 MGI 11440 Trp53 transformation related protein 53 gene MP:0012400 nail dystrophy IAGP N RGD:5509061 20141003 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20160204 MGI PMID:25815421 11440 Trp53 transformation related protein 53 gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20161222 MGI PMID:27354067 11440 Trp53 transformation related protein 53 gene MP:0012415 decreased sarcoma incidence IAGP N RGD:5509061 20151015 MGI PMID:25512531 11440 Trp53 transformation related protein 53 gene MP:0012415 decreased sarcoma incidence IAGP N RGD:5509061 20160915 MGI PMID:23412344 11440 Trp53 transformation related protein 53 gene MP:0012416 decreased gland tumor incidence IAGP N RGD:5509061 20231102 MGI PMID:36241718 11440 Trp53 transformation related protein 53 gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20200820 MGI PMID:32728212 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10346812 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10591653 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10760284 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10911993 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11169961 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11956084 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11967151 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12414647 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12914700 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12914701 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14702042 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15150107 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:1552940 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15607981 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15821748 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16227443 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16260620 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16357136 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16702401 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16751807 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17417627 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17452975 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17486075 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17510390 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17906694 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17984302 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18835033 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19767771 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19881536 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20473325 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20962274 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21324922 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21368836 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21799785 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22896338 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23665223 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23754438 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24029233 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24115439 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7922305 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141127 MGI PMID:9861017 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20151015 MGI PMID:25512531 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160225 MGI PMID:25144937 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160428 MGI PMID:16166291 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160602 MGI PMID:23459151 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160915 MGI PMID:23412344 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160915 MGI PMID:23538418 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20170608 MGI PMID:23979016 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20190711 MGI PMID:29635765 11440 Trp53 transformation related protein 53 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20230615 MGI PMID:23656786 11440 Trp53 transformation related protein 53 gene MP:0012690 abnormal stride length IAGP N RGD:5509061 20160609 MGI PMID:26363008 11440 Trp53 transformation related protein 53 gene MP:0013177 abnormal tail tip morphology IAGP N RGD:5509061 20141003 MGI PMID:24013501 11440 Trp53 transformation related protein 53 gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20141003 MGI PMID:15894267 11440 Trp53 transformation related protein 53 gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20150319 MGI PMID:22617326 11440 Trp53 transformation related protein 53 gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20150507 MGI PMID:23851502 11440 Trp53 transformation related protein 53 gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20241024 MGI PMID:31048544 11440 Trp53 transformation related protein 53 gene MP:0013236 ovary degeneration IAGP N RGD:5509061 20141003 MGI PMID:23741457 11440 Trp53 transformation related protein 53 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:16790550 11440 Trp53 transformation related protein 53 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20200423 MGI PMID:30858608 11440 Trp53 transformation related protein 53 gene MP:0013374 increased sebaceous gland tumor incidence IAGP N RGD:5509061 20180913 MGI PMID:24162662 11440 Trp53 transformation related protein 53 gene MP:0013483 abnormal jejunum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200820 MGI PMID:32728212 11440 Trp53 transformation related protein 53 gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16616333 11440 Trp53 transformation related protein 53 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17170753 11440 Trp53 transformation related protein 53 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:19620979 11440 Trp53 transformation related protein 53 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150219 MGI PMID:11431698 11440 Trp53 transformation related protein 53 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20190328 MGI PMID:30232008 11440 Trp53 transformation related protein 53 gene MP:0013505 decreased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17325035 11440 Trp53 transformation related protein 53 gene MP:0013539 increased ovary adenoma incidence IAGP N RGD:5509061 20161222 MGI PMID:27354067 11440 Trp53 transformation related protein 53 gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20180830 MGI PMID:29479066 11440 Trp53 transformation related protein 53 gene MP:0013696 increased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20180830 MGI PMID:29479066 11440 Trp53 transformation related protein 53 gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20150409 MGI PMID:19966810 11440 Trp53 transformation related protein 53 gene MP:0013705 decreased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20150409 MGI PMID:19966810 11440 Trp53 transformation related protein 53 gene MP:0013716 hypolactation IAGP N RGD:5509061 20190523 MGI PMID:21282721 11440 Trp53 transformation related protein 53 gene MP:0013751 increased cystadenoma incidence IAGP N RGD:5509061 20170615 MGI PMID:26411367 11440 Trp53 transformation related protein 53 gene MP:0013958 decreased small intestine length IAGP N RGD:5509061 20220721 MGI PMID:34376666 11440 Trp53 transformation related protein 53 gene MP:0014040 increased cellular sensitivity to DNA damaging agents IAGP N RGD:5509061 20181129 MGI PMID:30042151 11440 Trp53 transformation related protein 53 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:12642502 11440 Trp53 transformation related protein 53 gene MP:0014127 increased thymoma incidence IAGP N RGD:5509061 20160317 MGI PMID:21552324 11440 Trp53 transformation related protein 53 gene MP:0014127 increased thymoma incidence IAGP N RGD:5509061 20160317 MGI PMID:9584189 11440 Trp53 transformation related protein 53 gene MP:0014127 increased thymoma incidence IAGP N RGD:5509061 20180906 MGI PMID:25565005 11440 Trp53 transformation related protein 53 gene MP:0014234 decreased enterocyte apoptosis IAGP N RGD:5509061 20230323 MGI PMID:10097137 11440 Trp53 transformation related protein 53 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:21674502 11440 Trp53 transformation related protein 53 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:25985210 11440 Trp53 transformation related protein 53 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:29743593 11440 Trp53 transformation related protein 53 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:33594717 11440 Trp53 transformation related protein 53 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:35700263 11440 Trp53 transformation related protein 53 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230615 MGI PMID:28655788 11440 Trp53 transformation related protein 53 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230615 MGI PMID:34803166 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:10077642 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:10346812 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:10760284 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:10973261 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:12839925 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:14647411 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:14702042 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:15231717 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:15652750 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:17417627 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:17533180 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:17906694 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:18202109 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:19767771 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:21277975 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:21285512 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:22341455 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:22411819 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:22682249 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:22896338 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:23285300 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:24029233 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:24120138 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:24292676 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:24711431 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:29743593 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:31483066 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:35700263 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:7922305 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230615 MGI PMID:23656786 11440 Trp53 transformation related protein 53 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230615 MGI PMID:34803166 11440 Trp53 transformation related protein 53 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0020069 decreased neocortex size IAGP N RGD:5509061 20240718 MGI PMID:34237032 11440 Trp53 transformation related protein 53 gene MP:0020386 adipose tissue inflammation IAGP N RGD:5509061 20161117 MGI PMID:21411755 11440 Trp53 transformation related protein 53 gene MP:0020410 increased liposarcoma incidence IAGP N RGD:5509061 20180111 MGI PMID:22293175 11440 Trp53 transformation related protein 53 gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20210422 MGI PMID:32381628 11440 Trp53 transformation related protein 53 gene MP:0021056 abnormal tumor vascular morphology IAGP N RGD:5509061 20230601 MGI PMID:35700263 11440 Trp53 transformation related protein 53 gene MP:0021085 increased DNA replication IAGP N RGD:5509061 20220310 MGI PMID:15607981 11440 Trp53 transformation related protein 53 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:10393064 11440 Trp53 transformation related protein 53 gene MP:0021184 decreased bone mineral density of humerus IAGP N RGD:5509061 20220915 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:15231717 11440 Trp53 transformation related protein 53 gene MP:0030073 square face IAGP N RGD:5509061 20170921 MGI PMID:25119037 11440 Trp53 transformation related protein 53 gene MP:0030737 decreased glutamic acid level IAGP N RGD:5509061 20191205 MGI PMID:31685994 11440 Trp53 transformation related protein 53 gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:22341455 11440 Trp53 transformation related protein 53 gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:23770245 11440 Trp53 transformation related protein 53 gene MP:0030928 increased telomere length IAGP N RGD:5509061 20190117 MGI PMID:22341455 11440 Trp53 transformation related protein 53 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:17607363 11440 Trp53 transformation related protein 53 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:24706806 11440 Trp53 transformation related protein 53 gene MP:0031058 hepatosplenomegaly IAGP N RGD:5509061 20230615 MGI PMID:23656786 11440 Trp53 transformation related protein 53 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:11780111 11440 Trp53 transformation related protein 53 gene MP:0031278 decreased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:29743593 11440 Trp53 transformation related protein 53 gene MP:0031278 decreased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:35700263 11440 Trp53 transformation related protein 53 gene MP:0031278 decreased osteosarcoma incidence IAGP N RGD:5509061 20230615 MGI PMID:28655788 11440 Trp53 transformation related protein 53 gene MP:0031278 decreased osteosarcoma incidence IAGP N RGD:5509061 20230615 MGI PMID:34803166 11445 Tpm1 tropomyosin 1, alpha gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20230601 MGI PMID:35243414 11445 Tpm1 tropomyosin 1, alpha gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9400381 11445 Tpm1 tropomyosin 1, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9440710 11445 Tpm1 tropomyosin 1, alpha gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20230601 MGI PMID:35243414 11445 Tpm1 tropomyosin 1, alpha gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20230601 MGI PMID:35243414 11445 Tpm1 tropomyosin 1, alpha gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20230601 MGI PMID:35243414 11445 Tpm1 tropomyosin 1, alpha gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20230601 MGI PMID:35243414 11445 Tpm1 tropomyosin 1, alpha gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9440710 11445 Tpm1 tropomyosin 1, alpha gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20230601 MGI PMID:35243414 11445 Tpm1 tropomyosin 1, alpha gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9400381 11445 Tpm1 tropomyosin 1, alpha gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20230601 MGI PMID:35243414 11445 Tpm1 tropomyosin 1, alpha gene MP:0012700 abnormal endocardial heart tube morphology IAGP N RGD:5509061 20230601 MGI PMID:35243414 11452 Trh thyrotropin releasing hormone gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 11452 Trh thyrotropin releasing hormone gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20181227 MGI 11452 Trh thyrotropin releasing hormone gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 11452 Trh thyrotropin releasing hormone gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20221215 MGI 11452 Trh thyrotropin releasing hormone gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 11452 Trh thyrotropin releasing hormone gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:9380725 11452 Trh thyrotropin releasing hormone gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9380725 11452 Trh thyrotropin releasing hormone gene MP:0002188 small heart IEA N RGD:5509061 20181227 MGI 11452 Trh thyrotropin releasing hormone gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9380725 11452 Trh thyrotropin releasing hormone gene MP:0002834 decreased heart weight IEA N RGD:5509061 20181227 MGI 11452 Trh thyrotropin releasing hormone gene MP:0002989 small kidney IEA N RGD:5509061 20181227 MGI 11452 Trh thyrotropin releasing hormone gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:9380725 11452 Trh thyrotropin releasing hormone gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141003 MGI PMID:10628753 11452 Trh thyrotropin releasing hormone gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141003 MGI PMID:9380725 11452 Trh thyrotropin releasing hormone gene MP:0005119 decreased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10628753 11452 Trh thyrotropin releasing hormone gene MP:0005135 increased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:9380725 11452 Trh thyrotropin releasing hormone gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20200402 MGI 11452 Trh thyrotropin releasing hormone gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220519 MGI 11452 Trh thyrotropin releasing hormone gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:10628753 11452 Trh thyrotropin releasing hormone gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20231207 MGI 11452 Trh thyrotropin releasing hormone gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 11453 Trhr thyrotropin releasing hormone receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150611 MGI PMID:25490146 11453 Trhr thyrotropin releasing hormone receptor gene MP:0001263 weight loss IAGP N RGD:5509061 20150611 MGI PMID:25490146 11453 Trhr thyrotropin releasing hormone receptor gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17666589 11453 Trhr thyrotropin releasing hormone receptor gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:17666589 11453 Trhr thyrotropin releasing hormone receptor gene MP:0003351 decreased circulating levels of thyroid hormone IAGP N RGD:5509061 20150611 MGI PMID:25490146 11453 Trhr thyrotropin releasing hormone receptor gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20150611 MGI PMID:25490146 11453 Trhr thyrotropin releasing hormone receptor gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:14988432 11453 Trhr thyrotropin releasing hormone receptor gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20150611 MGI PMID:25490146 11453 Trhr thyrotropin releasing hormone receptor gene MP:0005471 decreased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:14988432 11453 Trhr thyrotropin releasing hormone receptor gene MP:0005473 decreased triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:14988432 11453 Trhr thyrotropin releasing hormone receptor gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:17666589 11453 Trhr thyrotropin releasing hormone receptor gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20150611 MGI PMID:25490146 11453 Trhr thyrotropin releasing hormone receptor gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20150611 MGI PMID:25490146 11453 Trhr thyrotropin releasing hormone receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17666589 11453 Trhr thyrotropin releasing hormone receptor gene MP:0011611 abnormal circulating ghrelin level IAGP N RGD:5509061 20150611 MGI PMID:25490146 11453 Trhr thyrotropin releasing hormone receptor gene MP:0011612 increased circulating ghrelin level IAGP N RGD:5509061 20150611 MGI PMID:25490146 11453 Trhr thyrotropin releasing hormone receptor gene MP:0011613 decreased circulating ghrelin level IAGP N RGD:5509061 20150611 MGI PMID:25490146 11457 Tsc2 TSC complex subunit 2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:18316403 11457 Tsc2 TSC complex subunit 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:19357198 11457 Tsc2 TSC complex subunit 2 gene MP:0000275 heart hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10096549 11457 Tsc2 TSC complex subunit 2 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10491404 11457 Tsc2 TSC complex subunit 2 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19357198 11457 Tsc2 TSC complex subunit 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20399730 11457 Tsc2 TSC complex subunit 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21419848 11457 Tsc2 TSC complex subunit 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21419848 11457 Tsc2 TSC complex subunit 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:10096549 11457 Tsc2 TSC complex subunit 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17245776 11457 Tsc2 TSC complex subunit 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 11457 Tsc2 TSC complex subunit 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:22791749 11457 Tsc2 TSC complex subunit 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22791749 11457 Tsc2 TSC complex subunit 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18316403 11457 Tsc2 TSC complex subunit 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23359422 11457 Tsc2 TSC complex subunit 2 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20150709 MGI PMID:23820898 11457 Tsc2 TSC complex subunit 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20150702 MGI PMID:23250422 11457 Tsc2 TSC complex subunit 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20170223 MGI PMID:25155956 11457 Tsc2 TSC complex subunit 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21419848 11457 Tsc2 TSC complex subunit 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21419848 11457 Tsc2 TSC complex subunit 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21419848 11457 Tsc2 TSC complex subunit 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:18568033 11457 Tsc2 TSC complex subunit 2 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18568033 11457 Tsc2 TSC complex subunit 2 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19357198 11457 Tsc2 TSC complex subunit 2 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20150709 MGI PMID:23820898 11457 Tsc2 TSC complex subunit 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10096549 11457 Tsc2 TSC complex subunit 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17245776 11457 Tsc2 TSC complex subunit 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23359422 11457 Tsc2 TSC complex subunit 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10491404 11457 Tsc2 TSC complex subunit 2 gene MP:0002045 increased renal cystadenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10491404 11457 Tsc2 TSC complex subunit 2 gene MP:0002045 increased renal cystadenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19357198 11457 Tsc2 TSC complex subunit 2 gene MP:0002047 increased hepatic hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:10096549 11457 Tsc2 TSC complex subunit 2 gene MP:0002047 increased hepatic hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:10491404 11457 Tsc2 TSC complex subunit 2 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10491404 11457 Tsc2 TSC complex subunit 2 gene MP:0002049 increased extremity angiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10491404 11457 Tsc2 TSC complex subunit 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:21062901 11457 Tsc2 TSC complex subunit 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:21419848 11457 Tsc2 TSC complex subunit 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18316403 11457 Tsc2 TSC complex subunit 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21062901 11457 Tsc2 TSC complex subunit 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17245776 11457 Tsc2 TSC complex subunit 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18316403 11457 Tsc2 TSC complex subunit 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19357198 11457 Tsc2 TSC complex subunit 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23359422 11457 Tsc2 TSC complex subunit 2 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:21062901 11457 Tsc2 TSC complex subunit 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 11457 Tsc2 TSC complex subunit 2 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20150702 MGI PMID:23250422 11457 Tsc2 TSC complex subunit 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18316403 11457 Tsc2 TSC complex subunit 2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 11457 Tsc2 TSC complex subunit 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:18316403 11457 Tsc2 TSC complex subunit 2 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18568033 11457 Tsc2 TSC complex subunit 2 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:21737790 11457 Tsc2 TSC complex subunit 2 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:21737790 11457 Tsc2 TSC complex subunit 2 gene MP:0003064 decreased coping response IAGP N RGD:5509061 20150702 MGI PMID:23250422 11457 Tsc2 TSC complex subunit 2 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:18316403 11457 Tsc2 TSC complex subunit 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21062901 11457 Tsc2 TSC complex subunit 2 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19357198 11457 Tsc2 TSC complex subunit 2 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20170223 MGI PMID:25155956 11457 Tsc2 TSC complex subunit 2 gene MP:0003570 increased uterus leiomyoma incidence IAGP N RGD:5509061 20150709 MGI PMID:23820898 11457 Tsc2 TSC complex subunit 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17245776 11457 Tsc2 TSC complex subunit 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17245776 11457 Tsc2 TSC complex subunit 2 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:10096549 11457 Tsc2 TSC complex subunit 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10096549 11457 Tsc2 TSC complex subunit 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17245776 11457 Tsc2 TSC complex subunit 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19357198 11457 Tsc2 TSC complex subunit 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22791749 11457 Tsc2 TSC complex subunit 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:22791749 11457 Tsc2 TSC complex subunit 2 gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20150709 MGI PMID:23820898 11457 Tsc2 TSC complex subunit 2 gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20150709 MGI PMID:23820898 11457 Tsc2 TSC complex subunit 2 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:19357198 11457 Tsc2 TSC complex subunit 2 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:18316403 11457 Tsc2 TSC complex subunit 2 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:21062901 11457 Tsc2 TSC complex subunit 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18316403 11457 Tsc2 TSC complex subunit 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:10096549 11457 Tsc2 TSC complex subunit 2 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18316403 11457 Tsc2 TSC complex subunit 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18316403 11457 Tsc2 TSC complex subunit 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19357198 11457 Tsc2 TSC complex subunit 2 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20150709 MGI PMID:23820898 11457 Tsc2 TSC complex subunit 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20160519 MGI PMID:25880340 11457 Tsc2 TSC complex subunit 2 gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20150709 MGI PMID:23820898 11457 Tsc2 TSC complex subunit 2 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20170223 MGI PMID:25155956 11457 Tsc2 TSC complex subunit 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21062901 11457 Tsc2 TSC complex subunit 2 gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20150709 MGI PMID:23820898 11457 Tsc2 TSC complex subunit 2 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:18316403 11457 Tsc2 TSC complex subunit 2 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:23359422 11457 Tsc2 TSC complex subunit 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20160519 MGI PMID:25880340 11457 Tsc2 TSC complex subunit 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20170223 MGI PMID:25155956 11457 Tsc2 TSC complex subunit 2 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21062901 11457 Tsc2 TSC complex subunit 2 gene MP:0010294 increased kidney tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18316403 11457 Tsc2 TSC complex subunit 2 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17245776 11457 Tsc2 TSC complex subunit 2 gene MP:0010384 increased renal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10096549 11457 Tsc2 TSC complex subunit 2 gene MP:0010384 increased renal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10491404 11457 Tsc2 TSC complex subunit 2 gene MP:0010656 thick myocardium IAGP N RGD:5509061 20141003 MGI PMID:10096549 11457 Tsc2 TSC complex subunit 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23359422 11457 Tsc2 TSC complex subunit 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21419848 11457 Tsc2 TSC complex subunit 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17245776 11457 Tsc2 TSC complex subunit 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10491404 11457 Tsc2 TSC complex subunit 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19357198 11457 Tsc2 TSC complex subunit 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23359422 11457 Tsc2 TSC complex subunit 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10096549 11457 Tsc2 TSC complex subunit 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17245776 11457 Tsc2 TSC complex subunit 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17245776 11457 Tsc2 TSC complex subunit 2 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 11457 Tsc2 TSC complex subunit 2 gene MP:0013401 increased endometrial gland number IAGP N RGD:5509061 20150709 MGI PMID:23820898 11457 Tsc2 TSC complex subunit 2 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20170223 MGI PMID:25155956 11457 Tsc2 TSC complex subunit 2 gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20190711 MGI PMID:25155956 11457 Tsc2 TSC complex subunit 2 gene MP:0031407 increased Sertoli cell proliferation IAGP N RGD:5509061 20220630 MGI PMID:22791749 11458 Tshr thyroid stimulating hormone receptor gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:10575115 11458 Tshr thyroid stimulating hormone receptor gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20151112 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20151112 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0000547 short limbs IAGP N RGD:5509061 20151112 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11530227 11458 Tshr thyroid stimulating hormone receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11530227 11458 Tshr thyroid stimulating hormone receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11530227 11458 Tshr thyroid stimulating hormone receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7209519 11458 Tshr thyroid stimulating hormone receptor gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11530227 11458 Tshr thyroid stimulating hormone receptor gene MP:0001396 unidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:11530227 11458 Tshr thyroid stimulating hormone receptor gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:11530227 11458 Tshr thyroid stimulating hormone receptor gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7209519 11458 Tshr thyroid stimulating hormone receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12432094 11458 Tshr thyroid stimulating hormone receptor gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:12432094 11458 Tshr thyroid stimulating hormone receptor gene MP:0001922 reduced male fertility IEA N RGD:5509061 20141003 MGI 11458 Tshr thyroid stimulating hormone receptor gene MP:0001923 reduced female fertility IEA N RGD:5509061 20141003 MGI 11458 Tshr thyroid stimulating hormone receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:7209519 11458 Tshr thyroid stimulating hormone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:7209519 11458 Tshr thyroid stimulating hormone receptor gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:16780814 11458 Tshr thyroid stimulating hormone receptor gene MP:0002083 premature death IEA N RGD:5509061 20141003 MGI 11458 Tshr thyroid stimulating hormone receptor gene MP:0002876 abnormal thyroid gland physiology IAGP N RGD:5509061 20141003 MGI PMID:12432094 11458 Tshr thyroid stimulating hormone receptor gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20151112 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:12432094 11458 Tshr thyroid stimulating hormone receptor gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20160714 MGI PMID:21220306 11458 Tshr thyroid stimulating hormone receptor gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20151112 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:10575115 11458 Tshr thyroid stimulating hormone receptor gene MP:0003194 abnormal frequency of paradoxical sleep IAGP N RGD:5509061 20141003 MGI PMID:11690529 11458 Tshr thyroid stimulating hormone receptor gene MP:0003351 decreased circulating levels of thyroid hormone IAGP N RGD:5509061 20141003 MGI PMID:12432094 11458 Tshr thyroid stimulating hormone receptor gene MP:0003356 impaired luteinization IAGP N RGD:5509061 20141003 MGI PMID:11690529 11458 Tshr thyroid stimulating hormone receptor gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20151112 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0003501 iodide oxidation defect IAGP N RGD:5509061 20141003 MGI PMID:12432094 11458 Tshr thyroid stimulating hormone receptor gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:12432094 11458 Tshr thyroid stimulating hormone receptor gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20151112 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20151112 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0003718 maternal effect IEA N RGD:5509061 20141003 MGI 11458 Tshr thyroid stimulating hormone receptor gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:11690529 11458 Tshr thyroid stimulating hormone receptor gene MP:0004022 abnormal cone electrophysiology IEA N RGD:5509061 20141003 MGI 11458 Tshr thyroid stimulating hormone receptor gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10575115 11458 Tshr thyroid stimulating hormone receptor gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:10575115 11458 Tshr thyroid stimulating hormone receptor gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:10575115 11458 Tshr thyroid stimulating hormone receptor gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12432094 11458 Tshr thyroid stimulating hormone receptor gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:7209519 11458 Tshr thyroid stimulating hormone receptor gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20160714 MGI PMID:21220306 11458 Tshr thyroid stimulating hormone receptor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10570273 11458 Tshr thyroid stimulating hormone receptor gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12432094 11458 Tshr thyroid stimulating hormone receptor gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:7209519 11458 Tshr thyroid stimulating hormone receptor gene MP:0005135 increased thyroid-stimulating hormone level IAGP N RGD:5509061 20151112 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7209519 11458 Tshr thyroid stimulating hormone receptor gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:11690529 11458 Tshr thyroid stimulating hormone receptor gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:12432094 11458 Tshr thyroid stimulating hormone receptor gene MP:0005471 decreased thyroxine level IAGP N RGD:5509061 20151112 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:12432094 11458 Tshr thyroid stimulating hormone receptor gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:7209519 11458 Tshr thyroid stimulating hormone receptor gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:12432094 11458 Tshr thyroid stimulating hormone receptor gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20151112 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10570273 11458 Tshr thyroid stimulating hormone receptor gene MP:0008337 increased thyrotroph cell number IEA N RGD:5509061 20141127 MGI 11458 Tshr thyroid stimulating hormone receptor gene MP:0008974 proportional dwarf IEA N RGD:5509061 20141003 MGI 11458 Tshr thyroid stimulating hormone receptor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:11690529 11458 Tshr thyroid stimulating hormone receptor gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20160714 MGI PMID:21220306 11458 Tshr thyroid stimulating hormone receptor gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20151112 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20151112 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20171228 MGI PMID:18559984 11458 Tshr thyroid stimulating hormone receptor gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12432094 11458 Tshr thyroid stimulating hormone receptor gene MP:0011084 lethality at weaning, incomplete penetrance IEA N RGD:5509061 20141003 MGI 11458 Tshr thyroid stimulating hormone receptor gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20141003 MGI 11458 Tshr thyroid stimulating hormone receptor gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:11530227 11458 Tshr thyroid stimulating hormone receptor gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:10575115 11458 Tshr thyroid stimulating hormone receptor gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16780814 11458 Tshr thyroid stimulating hormone receptor gene MP:0012144 decreased b-wave amplitude IEA N RGD:5509061 20141003 MGI 11458 Tshr thyroid stimulating hormone receptor gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20151112 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:10575115 11458 Tshr thyroid stimulating hormone receptor gene MP:0014409 decreased distortion product otoacoustic emission amplitude IAGP N RGD:5509061 20240405 MGI PMID:10575115 11458 Tshr thyroid stimulating hormone receptor gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20151112 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0021194 decreased bone mineral density of caudal vertebrae IAGP N RGD:5509061 20220915 MGI PMID:17932107 11458 Tshr thyroid stimulating hormone receptor gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:11690529 11459 Tspy-ps testis specific protein-Y encoded, pseudogene gene MP:0003397 increased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:15851664 11459 Tspy-ps testis specific protein-Y encoded, pseudogene gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:15851664 11460 Tst thiosulfate sulfurtransferase, mitochondrial gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 11460 Tst thiosulfate sulfurtransferase, mitochondrial gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170105 MGI 11460 Tst thiosulfate sulfurtransferase, mitochondrial gene MP:0001147 small testis IEA N RGD:5509061 20170105 MGI 11460 Tst thiosulfate sulfurtransferase, mitochondrial gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 11460 Tst thiosulfate sulfurtransferase, mitochondrial gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 11460 Tst thiosulfate sulfurtransferase, mitochondrial gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20160811 MGI 11460 Tst thiosulfate sulfurtransferase, mitochondrial gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20160811 MGI 11460 Tst thiosulfate sulfurtransferase, mitochondrial gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20221215 MGI 11460 Tst thiosulfate sulfurtransferase, mitochondrial gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 11466 Tyr tyrosinase gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:521742 11466 Tyr tyrosinase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:1033984 11466 Tyr tyrosinase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:12215665 11466 Tyr tyrosinase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:15572362 11466 Tyr tyrosinase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:21968110 11466 Tyr tyrosinase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:4296364 11466 Tyr tyrosinase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:4823665 11466 Tyr tyrosinase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:6793688 11466 Tyr tyrosinase gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1822431 11466 Tyr tyrosinase gene MP:0000373 belly spot IEA N RGD:5509061 20120202 MGI 11466 Tyr tyrosinase gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20141003 MGI PMID:6793688 11466 Tyr tyrosinase gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20141003 MGI PMID:9023352 11466 Tyr tyrosinase gene MP:0000411 shiny fur IEA N RGD:5509061 20111116 MGI 11466 Tyr tyrosinase gene MP:0000421 mottled coat IAGP N RGD:5509061 20141003 MGI PMID:9023352 11466 Tyr tyrosinase gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:11925014 11466 Tyr tyrosinase gene MP:0001189 absent skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10325425 11466 Tyr tyrosinase gene MP:0001189 absent skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21943097 11466 Tyr tyrosinase gene MP:0001189 absent skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:6793688 11466 Tyr tyrosinase gene MP:0001189 absent skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8921397 11466 Tyr tyrosinase gene MP:0001224 abnormal keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16988713 11466 Tyr tyrosinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20181206 MGI PMID:18469339 11466 Tyr tyrosinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15489520 11466 Tyr tyrosinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20130004 11466 Tyr tyrosinase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20111116 MGI 11466 Tyr tyrosinase gene MP:0001304 cataract IEA N RGD:5509061 20111116 MGI 11466 Tyr tyrosinase gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15572362 11466 Tyr tyrosinase gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:20130004 11466 Tyr tyrosinase gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:12040030 11466 Tyr tyrosinase gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:15161869 11466 Tyr tyrosinase gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:15161869 11466 Tyr tyrosinase gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20181206 MGI PMID:18469339 11466 Tyr tyrosinase gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20181206 MGI PMID:18469339 11466 Tyr tyrosinase gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20180614 MGI 11466 Tyr tyrosinase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20181206 MGI PMID:17024248 11466 Tyr tyrosinase gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20181206 MGI PMID:17024248 11466 Tyr tyrosinase gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20181206 MGI PMID:18469339 11466 Tyr tyrosinase gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20181206 MGI PMID:17024248 11466 Tyr tyrosinase gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20111116 MGI 11466 Tyr tyrosinase gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:15489520 11466 Tyr tyrosinase gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:24124512 11466 Tyr tyrosinase gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:24124512 11466 Tyr tyrosinase gene MP:0001925 male infertility IEA N RGD:5509061 20120202 MGI 11466 Tyr tyrosinase gene MP:0001926 female infertility IEA N RGD:5509061 20180614 MGI 11466 Tyr tyrosinase gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:20130004 11466 Tyr tyrosinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1033984 11466 Tyr tyrosinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12955145 11466 Tyr tyrosinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1618394 11466 Tyr tyrosinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1822431 11466 Tyr tyrosinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:20130004 11466 Tyr tyrosinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4296364 11466 Tyr tyrosinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4823665 11466 Tyr tyrosinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8200511 11466 Tyr tyrosinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9023352 11466 Tyr tyrosinase gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:2304907 11466 Tyr tyrosinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21625383 11466 Tyr tyrosinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:574104 11466 Tyr tyrosinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7117820 11466 Tyr tyrosinase gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:11925014 11466 Tyr tyrosinase gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9023352 11466 Tyr tyrosinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24823394 11466 Tyr tyrosinase gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20181206 MGI PMID:18469339 11466 Tyr tyrosinase gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21494554 11466 Tyr tyrosinase gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20181206 MGI PMID:18469339 11466 Tyr tyrosinase gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20181206 MGI PMID:17024248 11466 Tyr tyrosinase gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:521742 11466 Tyr tyrosinase gene MP:0003136 yellow coat color IEA N RGD:5509061 20111116 MGI 11466 Tyr tyrosinase gene MP:0003234 enhanced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20130004 11466 Tyr tyrosinase gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:15489520 11466 Tyr tyrosinase gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:521742 11466 Tyr tyrosinase gene MP:0003604 single kidney IEA N RGD:5509061 20120202 MGI 11466 Tyr tyrosinase gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20120202 MGI 11466 Tyr tyrosinase gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:4141683 11466 Tyr tyrosinase gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21625383 11466 Tyr tyrosinase gene MP:0003962 abnormal adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:10212311 11466 Tyr tyrosinase gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:10212311 11466 Tyr tyrosinase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15489520 11466 Tyr tyrosinase gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20130004 11466 Tyr tyrosinase gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:4823665 11466 Tyr tyrosinase gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:4141683 11466 Tyr tyrosinase gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:4823665 11466 Tyr tyrosinase gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:12624268 11466 Tyr tyrosinase gene MP:0004222 iris synechia IAGP N RGD:5509061 20141003 MGI PMID:12624268 11466 Tyr tyrosinase gene MP:0004226 absent Schlemm's canal IAGP N RGD:5509061 20141003 MGI PMID:12624268 11466 Tyr tyrosinase gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:16988713 11466 Tyr tyrosinase gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21943097 11466 Tyr tyrosinase gene MP:0004382 abnormal hair follicle melanogenesis IAGP N RGD:5509061 20141003 MGI PMID:6793688 11466 Tyr tyrosinase gene MP:0004382 abnormal hair follicle melanogenesis IAGP N RGD:5509061 20141003 MGI PMID:7688401 11466 Tyr tyrosinase gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:15489520 11466 Tyr tyrosinase gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:15489520 11466 Tyr tyrosinase gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:15489520 11466 Tyr tyrosinase gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:21968110 11466 Tyr tyrosinase gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 11466 Tyr tyrosinase gene MP:0005077 abnormal melanogenesis IAGP N RGD:5509061 20141003 MGI PMID:4634048 11466 Tyr tyrosinase gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21968110 11466 Tyr tyrosinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10325425 11466 Tyr tyrosinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1352884 11466 Tyr tyrosinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1618394 11466 Tyr tyrosinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:20130004 11466 Tyr tyrosinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21968110 11466 Tyr tyrosinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:24879364 11466 Tyr tyrosinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4296364 11466 Tyr tyrosinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8200511 11466 Tyr tyrosinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141016 MGI PMID:24599260 11466 Tyr tyrosinase gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10325425 11466 Tyr tyrosinase gene MP:0005174 abnormal tail pigmentation IEA N RGD:5509061 20170209 MGI 11466 Tyr tyrosinase gene MP:0005198 abnormal aqueous drainage system morphology IAGP N RGD:5509061 20141003 MGI PMID:12624268 11466 Tyr tyrosinase gene MP:0005203 abnormal trabecular meshwork morphology IAGP N RGD:5509061 20141003 MGI PMID:12624268 11466 Tyr tyrosinase gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12040030 11466 Tyr tyrosinase gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:3596986 11466 Tyr tyrosinase gene MP:0005257 abnormal intraocular pressure IAGP N RGD:5509061 20141003 MGI PMID:11532192 11466 Tyr tyrosinase gene MP:0005366 variegated coat color IAGP N RGD:5509061 20141003 MGI PMID:15572362 11466 Tyr tyrosinase gene MP:0005408 hypopigmentation IEA N RGD:5509061 20111116 MGI 11466 Tyr tyrosinase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:10212311 11466 Tyr tyrosinase gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:15489520 11466 Tyr tyrosinase gene MP:0006159 ocular albinism IAGP N RGD:5509061 20141003 MGI PMID:18715234 11466 Tyr tyrosinase gene MP:0006159 ocular albinism IAGP N RGD:5509061 20141003 MGI PMID:21968110 11466 Tyr tyrosinase gene MP:0006159 ocular albinism IAGP N RGD:5509061 20141003 MGI PMID:9023352 11466 Tyr tyrosinase gene MP:0006370 abnormal hair follicle pheomelanosome pheomelanin content IEA N RGD:5509061 20141003 MGI 11466 Tyr tyrosinase gene MP:0008480 absent eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12215665 11466 Tyr tyrosinase gene MP:0008480 absent eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1618394 11466 Tyr tyrosinase gene MP:0008480 absent eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:24879364 11466 Tyr tyrosinase gene MP:0008480 absent eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8200511 11466 Tyr tyrosinase gene MP:0008480 absent eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9023352 11466 Tyr tyrosinase gene MP:0008480 absent eye pigmentation IAGP N RGD:5509061 20141016 MGI PMID:24599260 11466 Tyr tyrosinase gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:21494554 11466 Tyr tyrosinase gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20141003 MGI PMID:21494554 11466 Tyr tyrosinase gene MP:0008770 decreased survivor rate IEA N RGD:5509061 20111116 MGI 11466 Tyr tyrosinase gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20150514 MGI PMID:1063212 11466 Tyr tyrosinase gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20150514 MGI PMID:1063212 11466 Tyr tyrosinase gene MP:0009287 decreased abdominal fat pad weight IAGP N RGD:5509061 20181206 MGI PMID:18469339 11466 Tyr tyrosinase gene MP:0010192 abnormal retina melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 11466 Tyr tyrosinase gene MP:0010193 abnormal choroid melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 11466 Tyr tyrosinase gene MP:0010231 transverse fur striping IAGP N RGD:5509061 20141003 MGI PMID:1822431 11466 Tyr tyrosinase gene MP:0010727 increased glioblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21625383 11466 Tyr tyrosinase gene MP:0010769 abnormal survival IEA N RGD:5509061 20120202 MGI 11466 Tyr tyrosinase gene MP:0011002 enhanced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20130004 11466 Tyr tyrosinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20130004 11466 Tyr tyrosinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:574104 11466 Tyr tyrosinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7117820 11466 Tyr tyrosinase gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12215665 11466 Tyr tyrosinase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10212311 11466 Tyr tyrosinase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15489520 11466 Tyr tyrosinase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2304907 11466 Tyr tyrosinase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8200511 11466 Tyr tyrosinase gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:574104 11466 Tyr tyrosinase gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7117820 11466 Tyr tyrosinase gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:521742 11466 Tyr tyrosinase gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:574104 11466 Tyr tyrosinase gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7117820 11466 Tyr tyrosinase gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:24124512 11466 Tyr tyrosinase gene MP:0011233 abnormal vitamin A metabolism IAGP N RGD:5509061 20141003 MGI PMID:18606814 11466 Tyr tyrosinase gene MP:0011277 decreased tail pigmentation IEA N RGD:5509061 20170126 MGI 11466 Tyr tyrosinase gene MP:0011279 decreased ear pigmentation IEA N RGD:5509061 20170126 MGI 11466 Tyr tyrosinase gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20150430 MGI PMID:12624268 11466 Tyr tyrosinase gene MP:0011551 variegated eye pigmentation pattern IEA N RGD:5509061 20170126 MGI 11466 Tyr tyrosinase gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20141003 MGI PMID:15161869 11466 Tyr tyrosinase gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20141003 MGI PMID:15161869 11466 Tyr tyrosinase gene MP:0014375 increased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:20130004 11466 Tyr tyrosinase gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20181206 MGI PMID:18469339 11466 Tyr tyrosinase gene MP:0031434 increased miscarriage rate IEA N RGD:5509061 20220915 MGI 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0000436 abnormal head movements IAGP N RGD:5509061 20190425 MGI PMID:28093506 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0000745 tremors IAGP N RGD:5509061 20190425 MGI PMID:28093506 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:18787040 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20190425 MGI PMID:28093506 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:18393392 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:18393392 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20230119 MGI 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20190425 MGI PMID:28093506 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:18787040 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20190425 MGI PMID:28093506 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230119 MGI 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230119 MGI 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0002425 abnormal susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18787040 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:18787040 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0004083 polysyndactyly IEA N RGD:5509061 20230119 MGI 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20190425 MGI PMID:28093506 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:18393392 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20230119 MGI 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0005150 cachexia IAGP N RGD:5509061 20190425 MGI PMID:28093506 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20240523 MGI 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:18787040 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18787040 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20201119 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20190425 MGI PMID:28093506 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:11452127 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:18787040 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0009008 delayed estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:18787040 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0009012 short diestrus IAGP N RGD:5509061 20141003 MGI PMID:18787040 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0009014 prolonged proestrus IAGP N RGD:5509061 20141003 MGI PMID:18787040 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0009322 increased splenocyte apoptosis IAGP N RGD:5509061 20201119 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0009357 abnormal seizure response to inducing agent IAGP N RGD:5509061 20141003 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0009396 small endometrial glands IAGP N RGD:5509061 20150326 MGI PMID:18393392 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0009853 decreased Sertoli cell phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:18159085 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20190425 MGI PMID:28093506 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20150219 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20201119 MGI PMID:10227296 11467 Tyro3 TYRO3 protein tyrosine kinase 3 gene MP:0031168 abnormal brain thrombosis IAGP N RGD:5509061 20201119 MGI PMID:11452127 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0000018 small ears IEA N RGD:5509061 20141003 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:8248019 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:8248019 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:12644183 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:1303241 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:15415586 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:5726144 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0000372 irregular coat pigmentation IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0000423 delayed hair regrowth IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0000427 abnormal hair cycle IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20171109 MGI PMID:20460369 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0000440 domed cranium IEA N RGD:5509061 20141003 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20171109 MGI PMID:20460369 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20141003 MGI PMID:10192392 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:16827931 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17247639 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20171109 MGI PMID:6831040 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0001922 reduced male fertility IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0001923 reduced female fertility IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:8248019 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15415586 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17247639 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:2245917 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:5726144 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8248019 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:8248019 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:18354038 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0002630 abnormal endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:8248019 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17247639 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:5726144 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0002938 white spotting IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0003136 yellow coat color IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0003878 abnormal ear physiology IAGP N RGD:5509061 20141003 MGI PMID:8248019 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20171109 MGI PMID:6466874 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20171109 MGI PMID:6466874 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0004367 abnormal strial intermediate cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8248019 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:8248019 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0005071 enlarged hair follicle melanin granules IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0005072 abnormal hair follicle melanin granule morphology IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16827931 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18715234 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0005114 premature hair loss IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0005172 decreased eye pigmentation IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0005199 abnormal iris pigment epithelium IAGP N RGD:5509061 20141003 MGI PMID:10192392 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0005208 abnormal iris stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:10192392 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0005257 abnormal intraocular pressure IAGP N RGD:5509061 20141003 MGI PMID:16827931 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:6696991 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:6696991 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0006228 iris atrophy IAGP N RGD:5509061 20141003 MGI PMID:16827931 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10192392 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0008238 abnormal dorsoventral coat patterning IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0008731 abnormal hair shaft melanin granule morphology IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0008732 reduced hair shaft melanin granule number IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0008733 abnormal hair shaft melanin granule distribution IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20171109 MGI PMID:16219534 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0010192 abnormal retina melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0010193 abnormal choroid melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0011089 perinatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0011277 decreased tail pigmentation IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0011279 decreased ear pigmentation IEA N RGD:5509061 20111116 MGI 11468 Tyrp1 tyrosinase-related protein 1 gene MP:0012010 parturition failure IAGP N RGD:5509061 20191219 MGI PMID:1756209 11469 Ube2i ubiquitin-conjugating enzyme E2I gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20220811 MGI 11469 Ube2i ubiquitin-conjugating enzyme E2I gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 11469 Ube2i ubiquitin-conjugating enzyme E2I gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201022 MGI 11469 Ube2i ubiquitin-conjugating enzyme E2I gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 11469 Ube2i ubiquitin-conjugating enzyme E2I gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 11469 Ube2i ubiquitin-conjugating enzyme E2I gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16326389 11469 Ube2i ubiquitin-conjugating enzyme E2I gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 11469 Ube2i ubiquitin-conjugating enzyme E2I gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:16326389 11469 Ube2i ubiquitin-conjugating enzyme E2I gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 11469 Ube2i ubiquitin-conjugating enzyme E2I gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 11469 Ube2i ubiquitin-conjugating enzyme E2I gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16326389 11469 Ube2i ubiquitin-conjugating enzyme E2I gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16326389 11469 Ube2i ubiquitin-conjugating enzyme E2I gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11469 Ube2i ubiquitin-conjugating enzyme E2I gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 11474 Ucp3 uncoupling protein 3 (mitochondrial, proton carrier) gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:10748195 11474 Ucp3 uncoupling protein 3 (mitochondrial, proton carrier) gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:18713955 11474 Ucp3 uncoupling protein 3 (mitochondrial, proton carrier) gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:10748196 11474 Ucp3 uncoupling protein 3 (mitochondrial, proton carrier) gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:10748195 11474 Ucp3 uncoupling protein 3 (mitochondrial, proton carrier) gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18713955 11474 Ucp3 uncoupling protein 3 (mitochondrial, proton carrier) gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10748195 11474 Ucp3 uncoupling protein 3 (mitochondrial, proton carrier) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:10748195 11474 Ucp3 uncoupling protein 3 (mitochondrial, proton carrier) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:11707458 11474 Ucp3 uncoupling protein 3 (mitochondrial, proton carrier) gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18713955 11474 Ucp3 uncoupling protein 3 (mitochondrial, proton carrier) gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:10748196 11474 Ucp3 uncoupling protein 3 (mitochondrial, proton carrier) gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:11274222 11474 Ucp3 uncoupling protein 3 (mitochondrial, proton carrier) gene MP:0031414 decreased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:16455084 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:9162006 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:9162006 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:18281487 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18281487 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:9162006 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18281487 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18281487 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20548776 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18281487 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22411819 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18281487 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:11045570 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:22675208 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:9162006 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18281487 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18543320 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19497281 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0002277 abnormal respiratory mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:8897914 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20190627 MGI PMID:10470078 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:9162006 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0003115 abnormal respiratory system development IAGP N RGD:5509061 20141003 MGI PMID:22675208 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0004390 abnormal bronchoalveolar duct junction morphology IAGP N RGD:5509061 20141003 MGI PMID:22411819 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:9162006 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0005161 hematuria IAGP N RGD:5509061 20190627 MGI PMID:10470078 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22675208 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20190627 MGI PMID:10470078 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0005426 tachypnea IAGP N RGD:5509061 20141003 MGI PMID:18281487 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0005488 bronchial epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20548776 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18281487 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18281487 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:8897914 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0009148 pancreas necrosis IAGP N RGD:5509061 20141003 MGI PMID:9162006 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22411819 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20190627 MGI PMID:10470078 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0011566 abnormal complement protein level IAGP N RGD:5509061 20190627 MGI PMID:10470078 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:22411819 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:28513596 11475 Scgb1a1 secretoglobin, family 1A, member 1 gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:28513596 11477 Umod uromodulin gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17264314 11477 Umod uromodulin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180712 MGI PMID:28990932 11477 Umod uromodulin gene MP:0001263 weight loss IAGP N RGD:5509061 20190321 MGI PMID:24324041 11477 Umod uromodulin gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:15522986 11477 Umod uromodulin gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:17264314 11477 Umod uromodulin gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0001762 polyuria IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0001762 polyuria IAGP N RGD:5509061 20190321 MGI PMID:24324041 11477 Umod uromodulin gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20180712 MGI PMID:28990932 11477 Umod uromodulin gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20190321 MGI PMID:24324041 11477 Umod uromodulin gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:14665435 11477 Umod uromodulin gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0002829 abnormal juxtaglomerular apparatus morphology IAGP N RGD:5509061 20141003 MGI PMID:15522986 11477 Umod uromodulin gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:17898038 11477 Umod uromodulin gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0002963 decreased urine protein level IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0002987 abnormal urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:15522986 11477 Umod uromodulin gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:17898038 11477 Umod uromodulin gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20180712 MGI PMID:28990932 11477 Umod uromodulin gene MP:0003606 kidney failure IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0003606 kidney failure IAGP N RGD:5509061 20180712 MGI PMID:28990932 11477 Umod uromodulin gene MP:0003670 dilated renal glomerular capsule IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20180712 MGI PMID:28990932 11477 Umod uromodulin gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17898038 11477 Umod uromodulin gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20180712 MGI PMID:28990932 11477 Umod uromodulin gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:17898038 11477 Umod uromodulin gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0005360 urolithiasis IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0005527 increased renal glomerular filtration rate IAGP N RGD:5509061 20190321 MGI PMID:24324041 11477 Umod uromodulin gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:15522986 11477 Umod uromodulin gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:17264314 11477 Umod uromodulin gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20190321 MGI PMID:24324041 11477 Umod uromodulin gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:17264314 11477 Umod uromodulin gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20180712 MGI PMID:28990932 11477 Umod uromodulin gene MP:0005557 increased creatinine clearance IAGP N RGD:5509061 20190321 MGI PMID:24324041 11477 Umod uromodulin gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:15522986 11477 Umod uromodulin gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20190321 MGI PMID:24324041 11477 Umod uromodulin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17264314 11477 Umod uromodulin gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17264314 11477 Umod uromodulin gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20180712 MGI PMID:28990932 11477 Umod uromodulin gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:17264314 11477 Umod uromodulin gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20190321 MGI PMID:24324041 11477 Umod uromodulin gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20190321 MGI PMID:24324041 11477 Umod uromodulin gene MP:0006272 abnormal urine organic anion level IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:17898038 11477 Umod uromodulin gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20190321 MGI PMID:24324041 11477 Umod uromodulin gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:17264314 11477 Umod uromodulin gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20180712 MGI PMID:28990932 11477 Umod uromodulin gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17898038 11477 Umod uromodulin gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20190321 MGI PMID:24324041 11477 Umod uromodulin gene MP:0009644 uremia IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0009645 crystalluria IAGP N RGD:5509061 20141003 MGI PMID:17898038 11477 Umod uromodulin gene MP:0009810 increased urine uric acid level IAGP N RGD:5509061 20141003 MGI PMID:17898038 11477 Umod uromodulin gene MP:0009810 increased urine uric acid level IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17264314 11477 Umod uromodulin gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:19692485 11477 Umod uromodulin gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0011331 abnormal papillary duct morphology IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0011344 abnormal loop of Henle ascending limb thick segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15522986 11477 Umod uromodulin gene MP:0011344 abnormal loop of Henle ascending limb thick segment morphology IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20180712 MGI PMID:28990932 11477 Umod uromodulin gene MP:0011424 decreased urine uric acid level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0011424 decreased urine uric acid level IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0011431 increased urine flow rate IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0011432 decreased urine flow rate IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0011435 increased urine magnesium level IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0011435 increased urine magnesium level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:17898038 11477 Umod uromodulin gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20190321 MGI PMID:24324041 11477 Umod uromodulin gene MP:0011465 abnormal urine urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0011470 increased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:17264314 11477 Umod uromodulin gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20180628 MGI PMID:28325753 11477 Umod uromodulin gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0011735 increased urine ammonia level IAGP N RGD:5509061 20141003 MGI PMID:20591941 11477 Umod uromodulin gene MP:0011891 decreased circulating ferritin level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0011894 decreased circulating transferrin level IAGP N RGD:5509061 20141003 MGI PMID:23748428 11477 Umod uromodulin gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:17264314 11477 Umod uromodulin gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:17264314 11477 Umod uromodulin gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20190321 MGI PMID:24324041 11477 Umod uromodulin gene MP:0012046 decreased susceptibility to hypertension IAGP N RGD:5509061 20190321 MGI PMID:24324041 11477 Umod uromodulin gene MP:0013305 isosthenuria IAGP N RGD:5509061 20180712 MGI PMID:28990932 11477 Umod uromodulin gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:19692485 11477 Umod uromodulin gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20160421 MGI PMID:19692485 11477 Umod uromodulin gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20180712 MGI PMID:28990932 11477 Umod uromodulin gene MP:0030779 decreased urine citrate level IAGP N RGD:5509061 20181004 MGI PMID:20591941 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11257140 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11375415 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15769895 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11375415 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11375415 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:7539357 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:7587631 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:11257140 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:15769895 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17379066 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15769895 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15769895 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7539357 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7587631 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:7587631 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:11257141 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9322371 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7539357 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:7539357 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:7539357 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:7587631 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:15769895 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:17379066 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:15769895 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:17379066 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:11375415 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:7587631 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0003057 abnormal epicardium morphology IAGP N RGD:5509061 20141003 MGI PMID:7587631 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20160128 MGI PMID:26034041 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11257140 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11257140 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0004557 dilated allantois IAGP N RGD:5509061 20141003 MGI PMID:7539357 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11375415 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11257141 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11375415 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11375415 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11257140 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11257141 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11375415 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:7539357 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:7587631 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7539357 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11375415 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11257140 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11257140 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11257140 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:11257141 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:11257141 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11257141 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11257141 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11257140 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11257141 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11257140 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:15769895 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:7539357 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0010555 absent epicardium IAGP N RGD:5509061 20240229 MGI PMID:7539357 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:7539357 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:7587631 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7539357 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7587631 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9322371 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11375415 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0011825 decreased cell chemotaxis IAGP N RGD:5509061 20160128 MGI PMID:26034041 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0012299 hydropic allantois IAGP N RGD:5509061 20141003 MGI PMID:7587631 11481 Vcam1 vascular cell adhesion molecule 1 gene MP:0014472 impaired B cell migration IAGP N RGD:5509061 20240613 MGI PMID:11257140 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:11687634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:14584880 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17123805 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17959935 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20151001 MGI PMID:25147982 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17099775 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15976027 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:10746634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:11385068 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:11532865 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:11687634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:11697802 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:12089348 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:12122115 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:14584880 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:15998839 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:17959935 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:21947295 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:9275211 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20151001 MGI PMID:25147982 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:15976027 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:15998839 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:17123805 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20151001 MGI PMID:25147982 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:12122115 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:11851870 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:11171393 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:11851870 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12089348 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:15639181 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:17959935 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:21947295 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:9275211 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20240523 MGI 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17962355 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:11532865 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:17962355 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:17962355 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:9275211 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:15998839 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0000745 tremors IEA N RGD:5509061 20240523 MGI 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10746634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10746634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:16880407 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:11851870 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:16880407 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:11851870 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:9275211 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11687634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15998839 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21947295 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9275211 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17962355 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15639181 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001283 sparse vibrissae IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15639181 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15639181 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001406 abnormal gait IEA N RGD:5509061 20240523 MGI 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:15639181 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:15639181 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15639181 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20240523 MGI 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20151001 MGI PMID:25147982 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:17099775 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17275288 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21947295 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11851870 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15998839 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17959935 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9275211 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10746634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:10746634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:12122115 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001849 ear inflammation IAGP N RGD:5509061 20141003 MGI PMID:16880407 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11385068 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11385068 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11385068 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11385068 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:10746634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:10746634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11385068 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17551101 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10746634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10746634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:15639181 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:9275211 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002764 short tibia IAGP N RGD:5509061 20151001 MGI PMID:25147982 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12122115 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17275288 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17275289 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:11697802 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:14584880 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:9275211 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:10910362 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:11687634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:12089348 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:12122115 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:15998839 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:17123805 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:9275211 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20151001 MGI PMID:25147982 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:21947295 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:17123805 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:15998839 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:9275211 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003112 enlarged parathyroid gland IAGP N RGD:5509061 20141003 MGI PMID:9275211 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:11687634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:11851870 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:12089348 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:14584880 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:15976027 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:9275211 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003116 rickets IAGP N RGD:5509061 20151001 MGI PMID:25147982 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17275288 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:15639181 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:12122115 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15976027 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15998839 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:9275211 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:17123805 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17099775 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003432 increased activity of parathyroid IAGP N RGD:5509061 20141003 MGI PMID:12089348 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003432 increased activity of parathyroid IAGP N RGD:5509061 20141003 MGI PMID:21947295 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003432 increased activity of parathyroid IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003432 increased activity of parathyroid IAGP N RGD:5509061 20151001 MGI PMID:25147982 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003493 parathyroid gland hyperplasia IAGP N RGD:5509061 20151001 MGI PMID:25147982 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003639 abnormal response to vitamins IAGP N RGD:5509061 20141003 MGI PMID:12089348 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:21947295 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20141003 MGI PMID:11851870 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17551101 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:17974622 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:21947295 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:17959935 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:11697802 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:11532865 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17962355 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10746634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21947295 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:14584880 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:17959935 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17099775 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17551101 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005046 absent spleen white pulp IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17959935 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21947295 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005401 abnormal fat-soluble vitamin level IAGP N RGD:5509061 20141003 MGI PMID:11532865 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005401 abnormal fat-soluble vitamin level IAGP N RGD:5509061 20141003 MGI PMID:11697802 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:12089348 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005522 increased circulating atrial natriuretic factor IAGP N RGD:5509061 20141003 MGI PMID:21947295 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005581 abnormal renin activity IAGP N RGD:5509061 20141003 MGI PMID:17275289 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005582 increased renin activity IAGP N RGD:5509061 20141003 MGI PMID:12122115 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17275288 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17099775 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:12122115 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005636 abnormal mineral homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15976027 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0005636 abnormal mineral homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17099775 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12122115 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12122115 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21947295 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17275289 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:12122115 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0006375 increased circulating angiotensinogen level IAGP N RGD:5509061 20141003 MGI PMID:12122115 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:17959935 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20151001 MGI PMID:25147982 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:9275211 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:17959935 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17959935 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:12089348 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:17962355 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008650 abnormal interleukin-1 secretion IAGP N RGD:5509061 20141003 MGI PMID:17959935 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17959935 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17959935 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20240523 MGI 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:15639181 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0009257 dilated seminiferous tubule IAGP N RGD:5509061 20141003 MGI PMID:10746634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11697802 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:16476050 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11697802 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14584880 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17962355 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0010699 dilated hair follicle IAGP N RGD:5509061 20181129 MGI PMID:11851870 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0010699 dilated hair follicle IAGP N RGD:5509061 20181129 MGI PMID:9275211 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:21947295 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:11697802 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0010926 increased osteoid volume IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0011221 decreased intestinal calcium absorption IAGP N RGD:5509061 20141003 MGI PMID:11687634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:11687634 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:12089348 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:14584880 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:15998839 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:17099775 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:23389957 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:12122115 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0012175 flat face IAGP N RGD:5509061 20141003 MGI PMID:9241280 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20151001 MGI PMID:25147982 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:15998839 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0030575 decreased hair follicle cell proliferation IAGP N RGD:5509061 20181129 MGI PMID:11851870 11484 Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor gene MP:0031232 increased circulating angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:12122115 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14500363 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20399150 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:18497742 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18497742 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:18497742 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:19252526 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16510575 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11171994 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:14500363 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:11171994 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001138 abnormal uterine cervix squamous epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18474617 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:14500363 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:14500363 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11171994 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:15798202 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11171994 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:14500363 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16652107 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19252526 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:22977222 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:16652107 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:15489957 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16652107 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:9256442 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:16652107 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12628185 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:16510575 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16652107 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14500363 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:19252526 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18474617 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002047 increased hepatic hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:11171994 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002047 increased hepatic hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:14500363 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002047 increased hepatic hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:15798202 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11171994 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14500363 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20733101 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16510575 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11171994 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:11171994 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15798202 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:18474617 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:14500363 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20160211 MGI PMID:25417109 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:20733101 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:11171994 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:15798202 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9651579 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16652107 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:22977222 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:19340311 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20141003 MGI PMID:18474617 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003597 increased epididymal cystadenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18474617 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:16510575 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18497742 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16652107 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:18497742 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20733101 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9651579 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:18957870 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:14604887 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:19252526 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0004967 abnormal kidney epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18497742 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9256442 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:19340311 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:19340311 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20141003 MGI PMID:14500363 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:20733101 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:22977222 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:18957870 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:15798202 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18957870 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20733101 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20733101 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:9651579 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:15798202 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:15489957 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16652107 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9256442 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0009043 increased pancreas adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19340311 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18474617 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20150326 MGI PMID:19252526 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16977322 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18474617 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:22977222 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:18497742 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22977222 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19340311 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11171994 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9256442 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9651579 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16652107 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17992257 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19252526 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011286 decreased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:22464323 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20141003 MGI PMID:18497742 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011336 abnormal kidney pelvis urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18497742 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011372 decreased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18957870 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18497742 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011509 dilated glomerular capillary IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:16652107 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:20733101 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20141003 MGI PMID:20522651 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:16652107 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0014241 abnormal intracellular organelle physiology IAGP N RGD:5509061 20230615 MGI PMID:23541568 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:14500363 11485 Vhl von Hippel-Lindau tumor suppressor gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:9256442 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:21697765 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21697765 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21697765 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0001393 ataxia IEA N RGD:5509061 20141003 MGI 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20141003 MGI 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0001405 impaired coordination IEA N RGD:5509061 20141003 MGI 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20141003 MGI 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0001505 hunched posture IEA N RGD:5509061 20141003 MGI 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21697765 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21697765 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21697765 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:21697765 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:21697765 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21697765 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21697765 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:21697765 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0009476 enlarged cecum IAGP N RGD:5509061 20141003 MGI PMID:21697765 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21697765 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21697765 11486 Vipr1 vasoactive intestinal peptide receptor 1 gene MP:0031155 small intestine hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:21697765 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:11181696 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10221657 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11181696 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11181696 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12055243 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0002403 abnormal pre-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10221657 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11181696 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16361315 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0003134 increased late pro-B cell number IAGP N RGD:5509061 20240404 MGI PMID:12055243 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12055243 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0005022 abnormal immature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11181696 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:11181696 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:12055243 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11181696 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12055243 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16361315 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11181696 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12055243 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16361315 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12055243 11487 Vpreb1a V-set pre-B cell surrogate light chain 1A gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:11181696 11489 Foxn1 forkhead box N1 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17202317 11489 Foxn1 forkhead box N1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17202317 11489 Foxn1 forkhead box N1 gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8629026 11489 Foxn1 forkhead box N1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20111116 MGI 11489 Foxn1 forkhead box N1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:4929778 11489 Foxn1 forkhead box N1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:5639157 11489 Foxn1 forkhead box N1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:721133 11489 Foxn1 forkhead box N1 gene MP:0000322 increased granulocyte number IEA N RGD:5509061 20111116 MGI 11489 Foxn1 forkhead box N1 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:15610506 11489 Foxn1 forkhead box N1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:2288204 11489 Foxn1 forkhead box N1 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:12893877 11489 Foxn1 forkhead box N1 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:15610506 11489 Foxn1 forkhead box N1 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:21387539 11489 Foxn1 forkhead box N1 gene MP:0000580 deformed nails IAGP N RGD:5509061 20141003 MGI PMID:15610506 11489 Foxn1 forkhead box N1 gene MP:0000580 deformed nails IAGP N RGD:5509061 20141003 MGI PMID:21387539 11489 Foxn1 forkhead box N1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0000685 abnormal immune system morphology IEA N RGD:5509061 20111116 MGI 11489 Foxn1 forkhead box N1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:5784127 11489 Foxn1 forkhead box N1 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:721133 11489 Foxn1 forkhead box N1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:5784127 11489 Foxn1 forkhead box N1 gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20111116 MGI 11489 Foxn1 forkhead box N1 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:721133 11489 Foxn1 forkhead box N1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:19955175 11489 Foxn1 forkhead box N1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:22179202 11489 Foxn1 forkhead box N1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:5493276 11489 Foxn1 forkhead box N1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:6698273 11489 Foxn1 forkhead box N1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:8629026 11489 Foxn1 forkhead box N1 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:10878619 11489 Foxn1 forkhead box N1 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:4007044 11489 Foxn1 forkhead box N1 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:7405870 11489 Foxn1 forkhead box N1 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:8629026 11489 Foxn1 forkhead box N1 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141120 MGI PMID:25053428 11489 Foxn1 forkhead box N1 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20150319 MGI PMID:14528302 11489 Foxn1 forkhead box N1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:10878619 11489 Foxn1 forkhead box N1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:11259083 11489 Foxn1 forkhead box N1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:15699117 11489 Foxn1 forkhead box N1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:19955175 11489 Foxn1 forkhead box N1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:5639157 11489 Foxn1 forkhead box N1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:5784127 11489 Foxn1 forkhead box N1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:721133 11489 Foxn1 forkhead box N1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:8629026 11489 Foxn1 forkhead box N1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:8671685 11489 Foxn1 forkhead box N1 gene MP:0000705 athymia IAGP N RGD:5509061 20160204 MGI PMID:16972005 11489 Foxn1 forkhead box N1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:19955175 11489 Foxn1 forkhead box N1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:22072979 11489 Foxn1 forkhead box N1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:6698273 11489 Foxn1 forkhead box N1 gene MP:0000706 small thymus IAGP N RGD:5509061 20160324 MGI PMID:14528302 11489 Foxn1 forkhead box N1 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22072979 11489 Foxn1 forkhead box N1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:14528302 11489 Foxn1 forkhead box N1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:18824585 11489 Foxn1 forkhead box N1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19955175 11489 Foxn1 forkhead box N1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141120 MGI PMID:25053428 11489 Foxn1 forkhead box N1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20190919 MGI PMID:30982661 11489 Foxn1 forkhead box N1 gene MP:0000716 abnormal immune system cell morphology IEA N RGD:5509061 20111116 MGI 11489 Foxn1 forkhead box N1 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22072979 11489 Foxn1 forkhead box N1 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 11489 Foxn1 forkhead box N1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0001211 wrinkled skin IEA N RGD:5509061 20141003 MGI 11489 Foxn1 forkhead box N1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:2288204 11489 Foxn1 forkhead box N1 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:2288204 11489 Foxn1 forkhead box N1 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:2288204 11489 Foxn1 forkhead box N1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:2288204 11489 Foxn1 forkhead box N1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18064304 11489 Foxn1 forkhead box N1 gene MP:0001274 curly vibrissae IEA N RGD:5509061 20141003 MGI 11489 Foxn1 forkhead box N1 gene MP:0001279 wavy vibrissae IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0001283 sparse vibrissae IEA N RGD:5509061 20141003 MGI 11489 Foxn1 forkhead box N1 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:1287512 11489 Foxn1 forkhead box N1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0001790 abnormal immune system physiology IEA N RGD:5509061 20111116 MGI 11489 Foxn1 forkhead box N1 gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20111116 MGI 11489 Foxn1 forkhead box N1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22072979 11489 Foxn1 forkhead box N1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141120 MGI PMID:25053428 11489 Foxn1 forkhead box N1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20190919 MGI PMID:30982661 11489 Foxn1 forkhead box N1 gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:22179202 11489 Foxn1 forkhead box N1 gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20150205 MGI PMID:24715454 11489 Foxn1 forkhead box N1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:4929778 11489 Foxn1 forkhead box N1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15922720 11489 Foxn1 forkhead box N1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0001923 reduced female fertility IEA N RGD:5509061 20141003 MGI 11489 Foxn1 forkhead box N1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:8671685 11489 Foxn1 forkhead box N1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0001935 decreased litter size IEA N RGD:5509061 20141003 MGI 11489 Foxn1 forkhead box N1 gene MP:0002032 increased sarcoma incidence IEA N RGD:5509061 20111116 MGI 11489 Foxn1 forkhead box N1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12724523 11489 Foxn1 forkhead box N1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 11489 Foxn1 forkhead box N1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:22072979 11489 Foxn1 forkhead box N1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:1104226 11489 Foxn1 forkhead box N1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15922720 11489 Foxn1 forkhead box N1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7405870 11489 Foxn1 forkhead box N1 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12893877 11489 Foxn1 forkhead box N1 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20141003 MGI 11489 Foxn1 forkhead box N1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15694130 11489 Foxn1 forkhead box N1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14528302 11489 Foxn1 forkhead box N1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18824585 11489 Foxn1 forkhead box N1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11038184 11489 Foxn1 forkhead box N1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14528302 11489 Foxn1 forkhead box N1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19955175 11489 Foxn1 forkhead box N1 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:5428870 11489 Foxn1 forkhead box N1 gene MP:0002347 abnormal lymph node T cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:5784127 11489 Foxn1 forkhead box N1 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22179202 11489 Foxn1 forkhead box N1 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:19955175 11489 Foxn1 forkhead box N1 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:22179202 11489 Foxn1 forkhead box N1 gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:5784127 11489 Foxn1 forkhead box N1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9820556 11489 Foxn1 forkhead box N1 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14528302 11489 Foxn1 forkhead box N1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15922720 11489 Foxn1 forkhead box N1 gene MP:0002460 decreased immunoglobulin level IEA N RGD:5509061 20111116 MGI 11489 Foxn1 forkhead box N1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:721133 11489 Foxn1 forkhead box N1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0002722 abnormal immune system organ morphology IEA N RGD:5509061 20111116 MGI 11489 Foxn1 forkhead box N1 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:11259083 11489 Foxn1 forkhead box N1 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11259083 11489 Foxn1 forkhead box N1 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:15699117 11489 Foxn1 forkhead box N1 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:9820556 11489 Foxn1 forkhead box N1 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:721133 11489 Foxn1 forkhead box N1 gene MP:0003361 abnormal circulating gonadotropin level IAGP N RGD:5509061 20141003 MGI PMID:11259083 11489 Foxn1 forkhead box N1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18064304 11489 Foxn1 forkhead box N1 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:19955175 11489 Foxn1 forkhead box N1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:10767081 11489 Foxn1 forkhead box N1 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:22179202 11489 Foxn1 forkhead box N1 gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:22179202 11489 Foxn1 forkhead box N1 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17202317 11489 Foxn1 forkhead box N1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:2288204 11489 Foxn1 forkhead box N1 gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20141003 MGI PMID:2288204 11489 Foxn1 forkhead box N1 gene MP:0003811 abnormal hair cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:2288204 11489 Foxn1 forkhead box N1 gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:10878619 11489 Foxn1 forkhead box N1 gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:12893877 11489 Foxn1 forkhead box N1 gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:16791198 11489 Foxn1 forkhead box N1 gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:19955175 11489 Foxn1 forkhead box N1 gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:8629026 11489 Foxn1 forkhead box N1 gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:8671685 11489 Foxn1 forkhead box N1 gene MP:0003815 hairless IAGP N RGD:5509061 20160204 MGI PMID:16972005 11489 Foxn1 forkhead box N1 gene MP:0003848 brittle hair IEA N RGD:5509061 20141003 MGI 11489 Foxn1 forkhead box N1 gene MP:0004125 abnormal venule morphology IAGP N RGD:5509061 20141003 MGI PMID:5784127 11489 Foxn1 forkhead box N1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:9328433 11489 Foxn1 forkhead box N1 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:4929778 11489 Foxn1 forkhead box N1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:15694130 11489 Foxn1 forkhead box N1 gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:22179202 11489 Foxn1 forkhead box N1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20190919 MGI PMID:30982661 11489 Foxn1 forkhead box N1 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14528302 11489 Foxn1 forkhead box N1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20111116 MGI 11489 Foxn1 forkhead box N1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8629026 11489 Foxn1 forkhead box N1 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16791198 11489 Foxn1 forkhead box N1 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20150205 MGI PMID:24715454 11489 Foxn1 forkhead box N1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:4929778 11489 Foxn1 forkhead box N1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:14528302 11489 Foxn1 forkhead box N1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:15699117 11489 Foxn1 forkhead box N1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:5428870 11489 Foxn1 forkhead box N1 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9164958 11489 Foxn1 forkhead box N1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:14528302 11489 Foxn1 forkhead box N1 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22072979 11489 Foxn1 forkhead box N1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14528302 11489 Foxn1 forkhead box N1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18824585 11489 Foxn1 forkhead box N1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19955175 11489 Foxn1 forkhead box N1 gene MP:0005150 cachexia IEA N RGD:5509061 20111116 MGI 11489 Foxn1 forkhead box N1 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:1287512 11489 Foxn1 forkhead box N1 gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:1729694 11489 Foxn1 forkhead box N1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:721133 11489 Foxn1 forkhead box N1 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:1287512 11489 Foxn1 forkhead box N1 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15699117 11489 Foxn1 forkhead box N1 gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:10878619 11489 Foxn1 forkhead box N1 gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:22072979 11489 Foxn1 forkhead box N1 gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:8629026 11489 Foxn1 forkhead box N1 gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:15699117 11489 Foxn1 forkhead box N1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14528302 11489 Foxn1 forkhead box N1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18824585 11489 Foxn1 forkhead box N1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22179202 11489 Foxn1 forkhead box N1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18824585 11489 Foxn1 forkhead box N1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22179202 11489 Foxn1 forkhead box N1 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22072979 11489 Foxn1 forkhead box N1 gene MP:0008101 lymph node hypoplasia IEA N RGD:5509061 20111116 MGI 11489 Foxn1 forkhead box N1 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18824585 11489 Foxn1 forkhead box N1 gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:15699117 11489 Foxn1 forkhead box N1 gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20200813 MGI PMID:27641500 11489 Foxn1 forkhead box N1 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:2288204 11489 Foxn1 forkhead box N1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:9820556 11489 Foxn1 forkhead box N1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9820556 11489 Foxn1 forkhead box N1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:9820556 11489 Foxn1 forkhead box N1 gene MP:0008600 decreased circulating interleukin-2 level IAGP N RGD:5509061 20141003 MGI PMID:9820556 11489 Foxn1 forkhead box N1 gene MP:0008732 reduced hair shaft melanin granule number IAGP N RGD:5509061 20141003 MGI PMID:2288204 11489 Foxn1 forkhead box N1 gene MP:0008737 abnormal spleen physiology IAGP N RGD:5509061 20141003 MGI PMID:4929778 11489 Foxn1 forkhead box N1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:5784127 11489 Foxn1 forkhead box N1 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18824585 11489 Foxn1 forkhead box N1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:1729694 11489 Foxn1 forkhead box N1 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:15694130 11489 Foxn1 forkhead box N1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:15694130 11489 Foxn1 forkhead box N1 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19955175 11489 Foxn1 forkhead box N1 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:19955175 11489 Foxn1 forkhead box N1 gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14528302 11489 Foxn1 forkhead box N1 gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19955175 11489 Foxn1 forkhead box N1 gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22072979 11489 Foxn1 forkhead box N1 gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22179202 11489 Foxn1 forkhead box N1 gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20141120 MGI PMID:25053428 11489 Foxn1 forkhead box N1 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 11489 Foxn1 forkhead box N1 gene MP:0009801 abnormal hair cortex keratinization IAGP N RGD:5509061 20141003 MGI PMID:2288204 11489 Foxn1 forkhead box N1 gene MP:0010129 increased DN1 thymic pro-T cell number IAGP N RGD:5509061 20141003 MGI PMID:22072979 11489 Foxn1 forkhead box N1 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:9820556 11489 Foxn1 forkhead box N1 gene MP:0010250 absent thymus cortex IAGP N RGD:5509061 20141003 MGI PMID:14528302 11489 Foxn1 forkhead box N1 gene MP:0010268 decreased lymphoma incidence IEA N RGD:5509061 20111116 MGI 11489 Foxn1 forkhead box N1 gene MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:1729694 11489 Foxn1 forkhead box N1 gene MP:0010681 abnormal hair follicle bulb morphology IEA N RGD:5509061 20141003 MGI 11489 Foxn1 forkhead box N1 gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:2288204 11489 Foxn1 forkhead box N1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:5980117 11489 Foxn1 forkhead box N1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 11489 Foxn1 forkhead box N1 gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20141003 MGI 11489 Foxn1 forkhead box N1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15141078 11489 Foxn1 forkhead box N1 gene MP:0012399 short nails IAGP N RGD:5509061 20141003 MGI PMID:15610506 11489 Foxn1 forkhead box N1 gene MP:0012399 short nails IAGP N RGD:5509061 20141003 MGI PMID:21387539 11489 Foxn1 forkhead box N1 gene MP:0012400 nail dystrophy IAGP N RGD:5509061 20141003 MGI PMID:15610506 11489 Foxn1 forkhead box N1 gene MP:0012402 abnormal nail bed morphology IAGP N RGD:5509061 20141003 MGI PMID:21387539 11489 Foxn1 forkhead box N1 gene MP:0012403 abnormal nail plate morphology IAGP N RGD:5509061 20141003 MGI PMID:15610506 11489 Foxn1 forkhead box N1 gene MP:0012403 abnormal nail plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21387539 11489 Foxn1 forkhead box N1 gene MP:0012405 abnormal nail matrix morphology IAGP N RGD:5509061 20141003 MGI PMID:15610506 11489 Foxn1 forkhead box N1 gene MP:0012405 abnormal nail matrix morphology IAGP N RGD:5509061 20141003 MGI PMID:21387539 11489 Foxn1 forkhead box N1 gene MP:0013225 abnormal third pharyngeal pouch morphology IAGP N RGD:5509061 20141120 MGI PMID:25053428 11489 Foxn1 forkhead box N1 gene MP:0013587 absent thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:14528302 11489 Foxn1 forkhead box N1 gene MP:0014130 thymus cyst IAGP N RGD:5509061 20160324 MGI PMID:14528302 11489 Foxn1 forkhead box N1 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:1287512 11489 Foxn1 forkhead box N1 gene MP:0020935 decreased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:1232464 11489 Foxn1 forkhead box N1 gene MP:0020935 decreased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:185426 11489 Foxn1 forkhead box N1 gene MP:0030605 abnormal corneocyte morphology IAGP N RGD:5509061 20180628 MGI PMID:2288204 11489 Foxn1 forkhead box N1 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:1287512 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11920562 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:9811581 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000776 abnormal inferior colliculus morphology IEA N RGD:5509061 20111116 MGI 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:2205396 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000798 abnormal frontal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:2202907 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:23444360 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:2202907 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:2205396 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:2202907 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:2205396 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000854 abnormal cerebellum development IEA N RGD:5509061 20111116 MGI 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000867 abnormal cerebellum anterior vermis morphology IEA N RGD:5509061 20111116 MGI 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:2202907 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:23444360 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:23444360 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:2202907 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0001504 abnormal posture IEA N RGD:5509061 20111116 MGI 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:2202907 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0001522 impaired swimming IEA N RGD:5509061 20111116 MGI 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:2202907 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:23444360 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0003312 abnormal locomotor coordination IEA N RGD:5509061 20111116 MGI 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:23444360 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:2205396 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0004096 abnormal midbrain-hindbrain boundary development IAGP N RGD:5509061 20141003 MGI PMID:2205396 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0004097 abnormal cerebellar cortex morphology IEA N RGD:5509061 20111116 MGI 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0004143 muscle hypertonia IEA N RGD:5509061 20111116 MGI 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0004203 abnormal cranial flexure morphology IAGP N RGD:5509061 20141003 MGI PMID:2205396 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0004205 absent hyoid bone IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20141003 MGI PMID:9811581 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0004459 small alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0004814 reduced linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:23444360 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20221215 MGI 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20201022 MGI 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:23041177 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:9441669 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0006288 small otic capsule IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0008026 abnormal brain white matter morphology IEA N RGD:5509061 20111116 MGI 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0008913 weaving IEA N RGD:5509061 20111116 MGI 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23444360 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20181122 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0009845 abnormal neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2205396 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2202907 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9441669 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2202907 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:2205396 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:9441669 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:23444360 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20141003 MGI PMID:8555108 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0012516 absent metencephalon IAGP N RGD:5509061 20141003 MGI PMID:9441669 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0012785 decreased rhombomere 1 size IAGP N RGD:5509061 20141003 MGI PMID:2205396 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0012785 decreased rhombomere 1 size IAGP N RGD:5509061 20141003 MGI PMID:23444360 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20171005 MGI PMID:9353119 11491 Wnt1 wingless-type MMTV integration site family, member 1 gene MP:0030383 small presphenoid bone IAGP N RGD:5509061 20171207 MGI PMID:9353119 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:12569130 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12569130 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12569130 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:12569130 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12569130 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:21228006 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:12569130 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0001679 thin apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:12569130 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:12569130 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0001697 abnormal embryo size IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0001710 absent amniotic folds IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18171685 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0003895 increased ectoderm apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12569130 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:12569130 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:23469192 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0009593 absent chorion IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10431243 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0011206 absent visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:10431240 11492 Wnt3 wingless-type MMTV integration site family, member 3 gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:12569130 11493 Wt1 WT1 transcription factor gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:19411759 11493 Wt1 WT1 transcription factor gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:14603255 11493 Wt1 WT1 transcription factor gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:14603255 11493 Wt1 WT1 transcription factor gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:8395349 11493 Wt1 WT1 transcription factor gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20150625 MGI PMID:24732380 11493 Wt1 WT1 transcription factor gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:10469569 11493 Wt1 WT1 transcription factor gene MP:0001127 small ovary IAGP N RGD:5509061 20220519 MGI PMID:24009315 11493 Wt1 WT1 transcription factor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220519 MGI PMID:24009315 11493 Wt1 WT1 transcription factor gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:16877546 11493 Wt1 WT1 transcription factor gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:16877546 11493 Wt1 WT1 transcription factor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16245160 11493 Wt1 WT1 transcription factor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16877546 11493 Wt1 WT1 transcription factor gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:8395349 11493 Wt1 WT1 transcription factor gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20161013 MGI PMID:17071579 11493 Wt1 WT1 transcription factor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:20023660 11493 Wt1 WT1 transcription factor gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:20023660 11493 Wt1 WT1 transcription factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20023660 11493 Wt1 WT1 transcription factor gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:8395349 11493 Wt1 WT1 transcription factor gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:16245160 11493 Wt1 WT1 transcription factor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220519 MGI PMID:24009315 11493 Wt1 WT1 transcription factor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16877546 11493 Wt1 WT1 transcription factor gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15509792 11493 Wt1 WT1 transcription factor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15509792 11493 Wt1 WT1 transcription factor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19797313 11493 Wt1 WT1 transcription factor gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8395349 11493 Wt1 WT1 transcription factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12024052 11493 Wt1 WT1 transcription factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12640141 11493 Wt1 WT1 transcription factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16877546 11493 Wt1 WT1 transcription factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17525726 11493 Wt1 WT1 transcription factor gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:8395349 11493 Wt1 WT1 transcription factor gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:11509181 11493 Wt1 WT1 transcription factor gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:11509181 11493 Wt1 WT1 transcription factor gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:16877546 11493 Wt1 WT1 transcription factor gene MP:0002214 streak gonad IAGP N RGD:5509061 20141003 MGI PMID:11509181 11493 Wt1 WT1 transcription factor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16877546 11493 Wt1 WT1 transcription factor gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16877546 11493 Wt1 WT1 transcription factor gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:23502960 11493 Wt1 WT1 transcription factor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:15509792 11493 Wt1 WT1 transcription factor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:19797313 11493 Wt1 WT1 transcription factor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20220331 MGI PMID:30367465 11493 Wt1 WT1 transcription factor gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:11509181 11493 Wt1 WT1 transcription factor gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:14603255 11493 Wt1 WT1 transcription factor gene MP:0002989 small kidney IAGP N RGD:5509061 20150625 MGI PMID:24732380 11493 Wt1 WT1 transcription factor gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:11509181 11493 Wt1 WT1 transcription factor gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20220519 MGI PMID:24009315 11493 Wt1 WT1 transcription factor gene MP:0003357 impaired granulosa cell differentiation IAGP N RGD:5509061 20220519 MGI PMID:24009315 11493 Wt1 WT1 transcription factor gene MP:0003578 absent ovary IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0003626 kidney medulla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14603255 11493 Wt1 WT1 transcription factor gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0003675 kidney cyst IAGP N RGD:5509061 20150625 MGI PMID:24732380 11493 Wt1 WT1 transcription factor gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20023660 11493 Wt1 WT1 transcription factor gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:8395349 11493 Wt1 WT1 transcription factor gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20161013 MGI PMID:17071579 11493 Wt1 WT1 transcription factor gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20170302 MGI PMID:27642710 11493 Wt1 WT1 transcription factor gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:19411759 11493 Wt1 WT1 transcription factor gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20141003 MGI PMID:16877546 11493 Wt1 WT1 transcription factor gene MP:0004195 abnormal kidney calyx morphology IAGP N RGD:5509061 20141003 MGI PMID:14603255 11493 Wt1 WT1 transcription factor gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:14603255 11493 Wt1 WT1 transcription factor gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:14603255 11493 Wt1 WT1 transcription factor gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:16245160 11493 Wt1 WT1 transcription factor gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:20023660 11493 Wt1 WT1 transcription factor gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:8395349 11493 Wt1 WT1 transcription factor gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15509792 11493 Wt1 WT1 transcription factor gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19797313 11493 Wt1 WT1 transcription factor gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:23502960 11493 Wt1 WT1 transcription factor gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20141003 MGI PMID:10469569 11493 Wt1 WT1 transcription factor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11509181 11493 Wt1 WT1 transcription factor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:19797313 11493 Wt1 WT1 transcription factor gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19797313 11493 Wt1 WT1 transcription factor gene MP:0005327 abnormal mesangial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0005327 abnormal mesangial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0005327 abnormal mesangial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19797313 11493 Wt1 WT1 transcription factor gene MP:0005644 agonadal IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20170302 MGI PMID:27642710 11493 Wt1 WT1 transcription factor gene MP:0006415 absent testes IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0008138 absent podocyte foot process IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:15509792 11493 Wt1 WT1 transcription factor gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20220519 MGI PMID:24009315 11493 Wt1 WT1 transcription factor gene MP:0009322 increased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10469569 11493 Wt1 WT1 transcription factor gene MP:0009323 abnormal spleen development IAGP N RGD:5509061 20141003 MGI PMID:10469569 11493 Wt1 WT1 transcription factor gene MP:0009362 abnormal primary ovarian follicle morphology IAGP N RGD:5509061 20220519 MGI PMID:24009315 11493 Wt1 WT1 transcription factor gene MP:0010118 abnormal intermediate mesoderm morphology IAGP N RGD:5509061 20170302 MGI PMID:27642710 11493 Wt1 WT1 transcription factor gene MP:0010294 increased kidney tumor incidence IAGP N RGD:5509061 20150625 MGI PMID:24732380 11493 Wt1 WT1 transcription factor gene MP:0010500 myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20170302 MGI PMID:26739565 11493 Wt1 WT1 transcription factor gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20170302 MGI PMID:26739565 11493 Wt1 WT1 transcription factor gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:10469569 11493 Wt1 WT1 transcription factor gene MP:0010985 abnormal kidney mesenchyme morphology IAGP N RGD:5509061 20150625 MGI PMID:24732380 11493 Wt1 WT1 transcription factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14603255 11493 Wt1 WT1 transcription factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10469569 11493 Wt1 WT1 transcription factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11509181 11493 Wt1 WT1 transcription factor gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10469569 11493 Wt1 WT1 transcription factor gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17525726 11493 Wt1 WT1 transcription factor gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411759 11493 Wt1 WT1 transcription factor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12024052 11493 Wt1 WT1 transcription factor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16877546 11493 Wt1 WT1 transcription factor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20023660 11493 Wt1 WT1 transcription factor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8395349 11493 Wt1 WT1 transcription factor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10469569 11493 Wt1 WT1 transcription factor gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14603255 11493 Wt1 WT1 transcription factor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20170302 MGI PMID:26739565 11493 Wt1 WT1 transcription factor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20170302 MGI PMID:27642710 11493 Wt1 WT1 transcription factor gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:14603255 11493 Wt1 WT1 transcription factor gene MP:0011301 juxtaglomerular cell hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0011316 abnormal kidney interlobular artery morphology IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:19797313 11493 Wt1 WT1 transcription factor gene MP:0011366 absent metanephros IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14603255 11493 Wt1 WT1 transcription factor gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8395349 11493 Wt1 WT1 transcription factor gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:19797313 11493 Wt1 WT1 transcription factor gene MP:0011411 abnormal gonadal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:8395349 11493 Wt1 WT1 transcription factor gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:19797313 11493 Wt1 WT1 transcription factor gene MP:0011498 abnormal glomerular capsule parietal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19797313 11493 Wt1 WT1 transcription factor gene MP:0011500 decreased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0011868 podocyte microvillus transformation IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0011871 podocyte hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10077614 11493 Wt1 WT1 transcription factor gene MP:0011871 podocyte hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0011871 podocyte hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19797313 11493 Wt1 WT1 transcription factor gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20161013 MGI PMID:17071579 11493 Wt1 WT1 transcription factor gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20170302 MGI PMID:27642710 11493 Wt1 WT1 transcription factor gene MP:0012496 abnormal pleuropericardial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:22984617 11493 Wt1 WT1 transcription factor gene MP:0012515 abnormal heart apex morphology IAGP N RGD:5509061 20141003 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0012515 abnormal heart apex morphology IAGP N RGD:5509061 20141003 MGI PMID:8395349 11493 Wt1 WT1 transcription factor gene MP:0012684 abnormal pleural cavity morphology IAGP N RGD:5509061 20170302 MGI PMID:27642710 11493 Wt1 WT1 transcription factor gene MP:0013310 abnormal adrenal gland development IAGP N RGD:5509061 20141120 MGI PMID:18040647 11493 Wt1 WT1 transcription factor gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:24009315 11493 Wt1 WT1 transcription factor gene MP:0031590 abnormal epicardium development IAGP N RGD:5509061 20240229 MGI PMID:19369973 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0000160 kyphosis IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0000161 scoliosis IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20190530 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:12531011 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0000692 small spleen IAGP N RGD:5509061 20170413 MGI PMID:27798842 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9294146 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0000705 athymia IAGP N RGD:5509061 20170413 MGI PMID:27798842 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0000706 small thymus IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001147 small testis IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12531386 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170413 MGI PMID:27798842 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:14642570 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:12531386 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:16751807 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16751807 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:12810694 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8756720 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8756720 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9294146 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8756720 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001925 male infertility IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001926 female infertility IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12531386 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16751807 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16751807 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16751807 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16751807 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8756720 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0002145 abnormal T cell differentiation IEA N RGD:5509061 20190530 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:9294146 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12531011 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0002764 short tibia IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10716994 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0003393 decreased cardiac output IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:12531011 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12531386 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:9294146 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:12810694 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20190530 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:8756720 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0005270 abnormal zygomatic bone morphology IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16751807 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:8756720 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190530 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190530 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190530 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20190530 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8756720 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0008126 increased dendritic cell number IEA N RGD:5509061 20190530 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0008167 increased B-1a cell number IEA N RGD:5509061 20190530 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20190530 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20190530 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0008925 increased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:16751807 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:12531386 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16751807 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0010463 aorta stenosis IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0010580 decreased heart left ventricle size IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190530 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190530 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:9294146 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12531386 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170413 MGI PMID:27798842 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12531011 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0011952 decreased cardiac stroke volume IEA N RGD:5509061 20240523 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16751807 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20190530 MGI 11495 Xrcc5 X-ray repair complementing defective repair in Chinese hamster cells 5 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:14642570 11497 Ywhaq tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 11497 Ywhaq tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17145769 11497 Ywhaq tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17145769 11497 Ywhaq tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17145769 11497 Ywhaq tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:17145769 11497 Ywhaq tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:17145769 11497 Ywhaq tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17145769 11497 Ywhaq tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17145769 11497 Ywhaq tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17145769 11497 Ywhaq tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17145769 11497 Ywhaq tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17145769 11497 Ywhaq tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17145769 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20160421 MGI 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0000373 belly spot IAGP N RGD:5509061 20181227 MGI PMID:27001213 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20160811 MGI 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20160505 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20181227 MGI PMID:27001213 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20160505 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20160505 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20160505 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160505 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20160811 MGI 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20181227 MGI PMID:27001213 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20160505 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20160505 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20211021 MGI 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20160505 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20160505 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20160505 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20160505 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20181227 MGI PMID:27001213 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20160505 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20160505 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0010011 ectopic hippocampus pyramidal cells IAGP N RGD:5509061 20160505 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160505 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20181227 MGI PMID:27001213 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:22124272 11498 Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22124272 11500 Yy1 YY1 transcription factor gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16611997 11500 Yy1 YY1 transcription factor gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20181122 MGI PMID:22570637 11500 Yy1 YY1 transcription factor gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10490658 11500 Yy1 YY1 transcription factor gene MP:0000932 absent notochord IAGP N RGD:5509061 20240627 MGI PMID:22669107 11500 Yy1 YY1 transcription factor gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20220609 MGI PMID:21123818 11500 Yy1 YY1 transcription factor gene MP:0001127 small ovary IAGP N RGD:5509061 20220609 MGI PMID:21123818 11500 Yy1 YY1 transcription factor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220609 MGI PMID:21123818 11500 Yy1 YY1 transcription factor gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20220609 MGI PMID:21123818 11500 Yy1 YY1 transcription factor gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:16611997 11500 Yy1 YY1 transcription factor gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20240627 MGI PMID:22669107 11500 Yy1 YY1 transcription factor gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20240627 MGI PMID:22669107 11500 Yy1 YY1 transcription factor gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20141003 MGI PMID:10490658 11500 Yy1 YY1 transcription factor gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20240627 MGI PMID:22669107 11500 Yy1 YY1 transcription factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10490658 11500 Yy1 YY1 transcription factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20240627 MGI PMID:22669107 11500 Yy1 YY1 transcription factor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220609 MGI PMID:21123818 11500 Yy1 YY1 transcription factor gene MP:0001926 female infertility IAGP N RGD:5509061 20220609 MGI PMID:21123818 11500 Yy1 YY1 transcription factor gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:16611997 11500 Yy1 YY1 transcription factor gene MP:0001953 respiratory failure IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20181122 MGI PMID:22570637 11500 Yy1 YY1 transcription factor gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20240627 MGI PMID:22669107 11500 Yy1 YY1 transcription factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16611997 11500 Yy1 YY1 transcription factor gene MP:0002174 abnormal gastrulation movements IAGP N RGD:5509061 20240627 MGI PMID:22669107 11500 Yy1 YY1 transcription factor gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20240627 MGI PMID:22669107 11500 Yy1 YY1 transcription factor gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20220609 MGI PMID:21123818 11500 Yy1 YY1 transcription factor gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16611997 11500 Yy1 YY1 transcription factor gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20181122 MGI PMID:22570637 11500 Yy1 YY1 transcription factor gene MP:0004880 lung cyst IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0005072 abnormal hair follicle melanin granule morphology IAGP N RGD:5509061 20181122 MGI PMID:22570637 11500 Yy1 YY1 transcription factor gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20240627 MGI PMID:22669107 11500 Yy1 YY1 transcription factor gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20220609 MGI PMID:21123818 11500 Yy1 YY1 transcription factor gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0008021 increased blastoma incidence IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0008238 abnormal dorsoventral coat patterning IAGP N RGD:5509061 20181122 MGI PMID:22570637 11500 Yy1 YY1 transcription factor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20220609 MGI PMID:21123818 11500 Yy1 YY1 transcription factor gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20220609 MGI PMID:21123818 11500 Yy1 YY1 transcription factor gene MP:0009331 absent primitive node IAGP N RGD:5509061 20240627 MGI PMID:22669107 11500 Yy1 YY1 transcription factor gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:16611997 11500 Yy1 YY1 transcription factor gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20181122 MGI PMID:22570637 11500 Yy1 YY1 transcription factor gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20240627 MGI PMID:22669107 11500 Yy1 YY1 transcription factor gene MP:0010862 decreased respiratory mucosa goblet cell number IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0010883 trachea stenosis IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0010949 decreased club cell number IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16611997 11500 Yy1 YY1 transcription factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10490658 11500 Yy1 YY1 transcription factor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16611997 11500 Yy1 YY1 transcription factor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16611997 11500 Yy1 YY1 transcription factor gene MP:0011113 abnormal airway basal cell morphology IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0011124 increased primary ovarian follicle number IAGP N RGD:5509061 20220609 MGI PMID:21123818 11500 Yy1 YY1 transcription factor gene MP:0011130 absent tertiary ovarian follicles IAGP N RGD:5509061 20220609 MGI PMID:21123818 11500 Yy1 YY1 transcription factor gene MP:0011142 abnormal lung-associated mesenchyme development IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20240627 MGI PMID:22669107 11500 Yy1 YY1 transcription factor gene MP:0011627 decreased skin pigmentation IAGP N RGD:5509061 20181122 MGI PMID:22570637 11500 Yy1 YY1 transcription factor gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20181122 MGI PMID:22570637 11500 Yy1 YY1 transcription factor gene MP:0012197 impaired myofibroblast differentiation IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20240627 MGI PMID:22669107 11500 Yy1 YY1 transcription factor gene MP:0012724 absent head fold IAGP N RGD:5509061 20240627 MGI PMID:22669107 11500 Yy1 YY1 transcription factor gene MP:0014200 abnormal respiratory epithelium physiology IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0021106 abnormal secondary ovarian follicle morphology IAGP N RGD:5509061 20220609 MGI PMID:21123818 11500 Yy1 YY1 transcription factor gene MP:0030002 increased lung apoptosis IAGP N RGD:5509061 20170622 MGI PMID:26329601 11500 Yy1 YY1 transcription factor gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220609 MGI PMID:21123818 11500 Yy1 YY1 transcription factor gene MP:0031436 decreased copulatory plug deposition IAGP N RGD:5509061 20220922 MGI PMID:21123818 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0000727 absent CD8-positive, alpha-beta T cells IEA N RGD:5509061 20111116 MGI 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0001606 impaired hematopoiesis IEA N RGD:5509061 20161201 MGI 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17767948 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22761313 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9208839 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9208839 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9794398 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0001828 abnormal T cell activation IEA N RGD:5509061 20111116 MGI 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11567635 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17767948 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24164480 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9794398 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9794398 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24164480 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24164480 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9208839 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:17767948 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0002935 chronic joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0002936 joint swelling IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11514605 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0003790 absent CD4-positive, alpha-beta T cells IEA N RGD:5509061 20111116 MGI 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0003944 abnormal T cell subpopulation ratio IEA N RGD:5509061 20111116 MGI 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22761313 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0004917 abnormal T cell selection IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0004972 abnormal regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:24164480 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0005002 abnormal T cell clonal deletion IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17767948 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9208839 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:15750595 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:24164480 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11514605 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11514605 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008070 absent T cells IEA N RGD:5509061 20111116 MGI 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11567635 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17767948 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24164480 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14647385 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17767948 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24164480 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008233 abnormal pro-B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18356083 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:17767948 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008501 increased IgG2b level IEA N RGD:5509061 20111116 MGI 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:9794398 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:11514605 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:11514605 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:19841086 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:9794398 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20180215 MGI 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20180215 MGI 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20151112 MGI 11501 Zap70 zeta-chain (TCR) associated protein kinase gene MP:0030795 joint dislocation IAGP N RGD:5509061 20181018 MGI PMID:14647385 11502 Rnf112 ring finger protein 112 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20161013 MGI PMID:26212327 11502 Rnf112 ring finger protein 112 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 11502 Rnf112 ring finger protein 112 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20161013 MGI PMID:26212327 11502 Rnf112 ring finger protein 112 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 11502 Rnf112 ring finger protein 112 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20161013 MGI PMID:26212327 11502 Rnf112 ring finger protein 112 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20161013 MGI PMID:26212327 11502 Rnf112 ring finger protein 112 gene MP:0021018 decreased dendritic spine number IAGP N RGD:5509061 20211014 MGI PMID:26212327 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:17108173 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17108173 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17108173 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:17901218 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21893599 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19287387 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17108173 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20211021 MGI 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21893599 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20211028 MGI PMID:27511108 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:21893599 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0005237 abnormal olfactory tract morphology IAGP N RGD:5509061 20141003 MGI PMID:17108173 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17108173 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20211028 MGI PMID:27511108 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17108173 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:23431164 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:17108173 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:17108173 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0008129 absent brain internal capsule IAGP N RGD:5509061 20141003 MGI PMID:17901218 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:17108173 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:17901218 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0008232 abnormal cingulum morphology IAGP N RGD:5509061 20141003 MGI PMID:17108173 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21893599 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20210128 MGI 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0010654 slow Wallerian degeneration IAGP N RGD:5509061 20141003 MGI PMID:19287387 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0010859 abnormal anterior commissure pars anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:17108173 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0010860 abnormal anterior commissure pars posterior morphology IAGP N RGD:5509061 20141003 MGI PMID:17108173 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17108173 11503 Map3k12 mitogen-activated protein kinase kinase kinase 12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 11522747 Eae41_m experimental allergic encephalomyelitis susceptibility 41 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20160805 MGI Created by mouse qtl pipeline PMID:12517969 11522747 Eae41_m experimental allergic encephalomyelitis susceptibility 41 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20160805 MGI Created by mouse qtl pipeline PMID:12517969 11522747 Eae41_m experimental allergic encephalomyelitis susceptibility 41 (mouse) qtl MP:0006082 CNS inflammation IAGP N RGD:5509061 20160811 MGI PMID:12517969 12436784 Bend2 BEN domain containing 2 gene MP:0001147 small testis IAGP N RGD:5509061 20220804 MGI PMID:35613276 12436784 Bend2 BEN domain containing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20220804 MGI PMID:35613276 12436784 Bend2 BEN domain containing 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220804 MGI PMID:35613276 12436784 Bend2 BEN domain containing 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20220804 MGI PMID:35613276 12436784 Bend2 BEN domain containing 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220804 MGI PMID:35613276 12436820 S2bpcox16 synaptojanin 2 binding protein Cox16 readthrough gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20231207 MGI 12436820 S2bpcox16 synaptojanin 2 binding protein Cox16 readthrough gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 12436820 S2bpcox16 synaptojanin 2 binding protein Cox16 readthrough gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20240523 MGI 12436820 S2bpcox16 synaptojanin 2 binding protein Cox16 readthrough gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 12436820 S2bpcox16 synaptojanin 2 binding protein Cox16 readthrough gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20240523 MGI 12879483 Asp1_m audiogenic seizure prone 1 (mouse) qtl MP:0001399 hyperactivity IAGP N RGD:5509061 20170427 MGI PMID:7399258 12879483 Asp1_m audiogenic seizure prone 1 (mouse) qtl MP:0001496 audiogenic seizures IAGP N RGD:5509061 20170427 MGI PMID:7399258 12879483 Asp1_m audiogenic seizure prone 1 (mouse) qtl MP:0002083 premature death IAGP N RGD:5509061 20170427 MGI PMID:7399258 12879483 Asp1_m audiogenic seizure prone 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20170421 MGI Created by mouse qtl pipeline PMID:7399258 12879483 Asp1_m audiogenic seizure prone 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20170421 MGI Created by mouse qtl pipeline PMID:7399258 12879483 Asp1_m audiogenic seizure prone 1 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20170421 MGI Created by mouse qtl pipeline PMID:7399258 12879484 Asp2_m audiogenic seizure prone 2 (mouse) qtl MP:0001496 audiogenic seizures IAGP N RGD:5509061 20170427 MGI PMID:2052619 12879484 Asp2_m audiogenic seizure prone 2 (mouse) qtl MP:0001496 audiogenic seizures IAGP N RGD:5509061 20170427 MGI PMID:5698855 12879484 Asp2_m audiogenic seizure prone 2 (mouse) qtl MP:0002083 premature death IAGP N RGD:5509061 20170427 MGI PMID:2052619 12879484 Asp2_m audiogenic seizure prone 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20170421 MGI Created by mouse qtl pipeline PMID:5698855|PMID:5527661 12879484 Asp2_m audiogenic seizure prone 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20170421 MGI Created by mouse qtl pipeline PMID:5698855|PMID:5527661 12879484 Asp2_m audiogenic seizure prone 2 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20170421 MGI Created by mouse qtl pipeline PMID:5698855|PMID:5527661 12879484 Asp2_m audiogenic seizure prone 2 (mouse) qtl MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:2052619 12904746 Litsq1_m litter size QTL 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20170519 MGI Created by mouse qtl pipeline PMID:18239664 12910120 Mahl_m modifier of age related hearing loss (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20170616 MGI Created by mouse qtl pipeline PMID:28287619 12910120 Mahl_m modifier of age related hearing loss (mouse) qtl MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20170615 MGI PMID:28287619 12910120 Mahl_m modifier of age related hearing loss (mouse) qtl MP:0005377 hearing/vestibular/ear phenotype IEA N RGD:704405 20170616 MGI Created by mouse qtl pipeline PMID:28287619 12910120 Mahl_m modifier of age related hearing loss (mouse) qtl MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20170615 MGI PMID:28287619 1300528 Ssial3_m susceptibility to sialadenitis 3 (mouse) qtl MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20111116 MGI PMID:11937580 1300528 Ssial3_m susceptibility to sialadenitis 3 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11937580 1300528 Ssial3_m susceptibility to sialadenitis 3 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11937580 1300528 Ssial3_m susceptibility to sialadenitis 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11937580 1300529 Idd9.3_m insulin dependent diabetes susceptibility 9.3 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:10933399 1300529 Idd9.3_m insulin dependent diabetes susceptibility 9.3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10933399 1300530 Livq2_m percent liver QTL 2 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:10353911 1300530 Livq2_m percent liver QTL 2 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1300530 Livq2_m percent liver QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:10353911 1300532 Tbs2_m tuberculosis severity 2 (mouse) qtl MP:0001263 weight loss IAGP N RGD:5509061 20111116 MGI PMID:12496157 1300532 Tbs2_m tuberculosis severity 2 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:12496157 1300532 Tbs2_m tuberculosis severity 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353873 1300532 Tbs2_m tuberculosis severity 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353873 1300533 Aem3_m anti-erythrocyte autoantibody modifier 3 (mouse) qtl MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20111116 MGI PMID:10607744 1300533 Aem3_m anti-erythrocyte autoantibody modifier 3 (mouse) qtl MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:10607744 1300533 Aem3_m anti-erythrocyte autoantibody modifier 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10607744 1300534 Bmd15_m bone mineral density 15 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:11450694 1300534 Bmd15_m bone mineral density 15 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11450694 1300535 Char3_m P. chabaudi malaria resistance QTL 3 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:10630291 1300535 Char3_m P. chabaudi malaria resistance QTL 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15170228|PMID:10630291 1300535 Char3_m P. chabaudi malaria resistance QTL 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:10630291 1300537 Ap3q_m alcohol preference 3 QTL (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:9726281 1300537 Ap3q_m alcohol preference 3 QTL (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9726281 1300538 Disso2_m dissociation of activity 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11381025 1300538 Disso2_m dissociation of activity 2 (mouse) qtl MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:11381025 1300540 Igfbp3q1_m insulin-like growth factor binding protein 3 QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11292658 1300540 Igfbp3q1_m insulin-like growth factor binding protein 3 QTL 1 (mouse) qtl MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20111116 MGI PMID:11292658 1300542 Lbm7_m lean body mass 7 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:12185457 1300542 Lbm7_m lean body mass 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12185457 1300544 Hypn_m hyperinsulinemia (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:12765967 1300544 Hypn_m hyperinsulinemia (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:15561960 1300544 Hypn_m hyperinsulinemia (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12765967 1300545 Lifespan3_m life span 3 (mouse) qtl MP:0001661 extended life span IAGP N RGD:5509061 20111116 MGI PMID:11773201 1300545 Lifespan3_m life span 3 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11773201 1300547 Cypr2_m cytokine production 2 (mouse) qtl MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20111116 MGI PMID:9887350 1300547 Cypr2_m cytokine production 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9887350 1300548 Adaz1_m anti-dsDNA antibody production in NZM 1 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:11513551 1300548 Adaz1_m anti-dsDNA antibody production in NZM 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11513551 1300549 Bbaa17_m B. burgdorferi-associated arthritis 17 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11704805 1300549 Bbaa17_m B. burgdorferi-associated arthritis 17 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11704805 1300550 Szv2_m seizure severity 2 (mouse) qtl MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20111116 MGI PMID:9069121 1300550 Szv2_m seizure severity 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9069121 1300550 Szv2_m seizure severity 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9069121 1300551 Lprm3_m lymphoproliferation modifier 3 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:9403730 1300551 Lprm3_m lymphoproliferation modifier 3 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9403730 1300551 Lprm3_m lymphoproliferation modifier 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9403730 1300552 Lrnx8_m learning-contextual 8 (mouse) qtl MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20111116 MGI PMID:9354800 1300552 Lrnx8_m learning-contextual 8 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9354800 1300553 Athsq1_m atherosclerosis susceptibility QTL 1 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:11438740 1300553 Athsq1_m atherosclerosis susceptibility QTL 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17641228|PMID:11438740 1300553 Athsq1_m atherosclerosis susceptibility QTL 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20150206 MGI Created by mouse qtl pipeline PMID:11438740 1300554 Giq1_m glucose intolerance QTL 1 (mouse) qtl MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20111116 MGI PMID:12439655 1300554 Giq1_m glucose intolerance QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12439655 1300556 Cia6_m collagen induced arthritis QTL 6 (mouse) qtl MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10453039 1300556 Cia6_m collagen induced arthritis QTL 6 (mouse) qtl MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10453039 1300556 Cia6_m collagen induced arthritis QTL 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10453039 1300558 Bw5_m body weight QTL 5 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:9725853 1300558 Bw5_m body weight QTL 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089|PMID:9725853 1300558 Bw5_m body weight QTL 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:9725853 1300560 Tgl1_m triglyceride level 1 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:11473059 1300560 Tgl1_m triglyceride level 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11473059 1300561 Heal7_m wound healing/regeneration 7 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:9751744 1300561 Heal7_m wound healing/regeneration 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12682777|PMID:9751744 1300561 Heal7_m wound healing/regeneration 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:9751744 1300563 Pgia5_m proteoglycan induced arthritis 5 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10615997 1300563 Pgia5_m proteoglycan induced arthritis 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10615997|PMID:15084914 1300563 Pgia5_m proteoglycan induced arthritis 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150925 MGI Created by mouse qtl pipeline PMID:10615997 1300564 Hlq5_m heat loss QTL 5 (mouse) qtl MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20111116 MGI PMID:10353911 1300564 Hlq5_m heat loss QTL 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1300565 Batq1_m brown fat QTL 1 (mouse) qtl MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:10353911 1300565 Batq1_m brown fat QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1300567 Bwq3_m body weight (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11515095 1300567 Bwq3_m body weight (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11515095 1300568 Hdl1_m high density lipoprotein (HDL) level 1 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:11108726 1300568 Hdl1_m high density lipoprotein (HDL) level 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11108726|PMID:12588951 1300568 Hdl1_m high density lipoprotein (HDL) level 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:11108726 1300569 Eae6b_m susceptibility to experimental allergic encephalomyelitis 6b (mouse) qtl MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:10438970 1300569 Eae6b_m susceptibility to experimental allergic encephalomyelitis 6b (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9712054 1300573 Elsgp2_m elevated serum gp70 2 (mouse) qtl MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20111116 MGI PMID:10903778 1300573 Elsgp2_m elevated serum gp70 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10903778 1300574 Im2_m immunoregulatory 2 (mouse) qtl MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20111116 MGI PMID:11058581 1300574 Im2_m immunoregulatory 2 (mouse) qtl MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20111116 MGI PMID:8962125 1300574 Im2_m immunoregulatory 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11058581 1300576 Yaail_m Yaa interacting locus (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:9862363 1300576 Yaail_m Yaa interacting locus (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:9862363 1300576 Yaail_m Yaa interacting locus (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9862363 1300576 Yaail_m Yaa interacting locus (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9862363 1300577 Capsq1_m capsaicin sensitivity related QTL 1 (mouse) qtl MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20111116 MGI PMID:14499433 1300577 Capsq1_m capsaicin sensitivity related QTL 1 (mouse) qtl MP:0005394 taste/olfaction phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14499433 1300578 Cd8ts3_m CD8 T cell subset 3 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12595899 1300578 Cd8ts3_m CD8 T cell subset 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300578 Cd8ts3_m CD8 T cell subset 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300578 Cd8ts3_m CD8 T cell subset 3 (mouse) qtl MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20111116 MGI PMID:12595899 1300579 Thypr1_m thymocyte proliferative response 1 (mouse) qtl MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:12044964 1300579 Thypr1_m thymocyte proliferative response 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12044964 1300579 Thypr1_m thymocyte proliferative response 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12044964 1300579 Thypr1_m thymocyte proliferative response 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12044964 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0001785 edema IAGP N RGD:5509061 20111116 MGI PMID:15814738 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0001805 decreased IgG level IAGP N RGD:5509061 20111116 MGI PMID:15814738 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0001806 decreased IgM level IAGP N RGD:5509061 20111116 MGI PMID:15814738 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0002083 premature death IAGP N RGD:5509061 20111116 MGI PMID:15814738 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0002083 premature death IAGP N RGD:5509061 20111116 MGI PMID:7937857 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0002083 premature death IAGP N RGD:5509061 20111116 MGI PMID:9449705 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:7937857 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:9449705 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0002962 increased urine protein level IAGP N RGD:5509061 20111116 MGI PMID:15814738 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:15814738 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:15814738 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20111116 MGI PMID:15814738 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:15814738 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7937857 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20170127 MGI Created by mouse qtl pipeline PMID:22371393|PMID:7937857 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7937857 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20170127 MGI Created by mouse qtl pipeline PMID:22371393|PMID:7937857 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:7937857 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7937857 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20170127 MGI Created by mouse qtl pipeline PMID:22371393|PMID:7937857 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7937857 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20170127 MGI Created by mouse qtl pipeline PMID:22371393|PMID:7937857 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7937857 1300580 Lbw2_m lupus NZB x NZW 2 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20170127 MGI Created by mouse qtl pipeline PMID:22371393|PMID:7937857 1300581 Tbrs1_m tuberculosis resistance 1 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:11197687 1300581 Tbrs1_m tuberculosis resistance 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11197687 1300583 Pbwg2_m postnatal body weight growth 2 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 1300583 Pbwg2_m postnatal body weight growth 2 (mouse) qtl MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20111116 MGI PMID:15056934 1300583 Pbwg2_m postnatal body weight growth 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15056934 1300585 Pgia12_m proteoglycan induced arthritis 12 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10615997 1300585 Pgia12_m proteoglycan induced arthritis 12 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10615997|PMID:15084914 1300585 Pgia12_m proteoglycan induced arthritis 12 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150925 MGI Created by mouse qtl pipeline PMID:10615997 1300586 Cdcs5_m cytokine deficiency colitis susceptibility 5 (mouse) qtl MP:0001858 intestinal inflammation IAGP N RGD:5509061 20111116 MGI PMID:11707574 1300586 Cdcs5_m cytokine deficiency colitis susceptibility 5 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11707574 1300586 Cdcs5_m cytokine deficiency colitis susceptibility 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11707574 1300591 Pas3_m pulmonary adenoma susceptibility 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7894154|PMID:7813906 1300592 Pcyts5_m plasmacytoma susceptibility 5 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12149518 1300592 Pcyts5_m plasmacytoma susceptibility 5 (mouse) qtl MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20111116 MGI PMID:12149518 1300593 Skull4_m skull morphology 4 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1300593 Skull4_m skull morphology 4 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300593 Skull4_m skull morphology 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300594 Eae2_m susceptibility to experimental allergic encephalomyelitis 2 (mouse) qtl MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20111116 MGI PMID:15611280 1300594 Eae2_m susceptibility to experimental allergic encephalomyelitis 2 (mouse) qtl MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:15611280 1300594 Eae2_m susceptibility to experimental allergic encephalomyelitis 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7545492 1300594 Eae2_m susceptibility to experimental allergic encephalomyelitis 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7545492 1300597 Skull14_m skull morphology 14 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1300597 Skull14_m skull morphology 14 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300597 Skull14_m skull morphology 14 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300598 Disso1_m dissociation of activity 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11381025 1300598 Disso1_m dissociation of activity 1 (mouse) qtl MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:11381025 1300600 Hdl2_m high density lipoprotein (HDL) level 2 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:11108726 1300600 Hdl2_m high density lipoprotein (HDL) level 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11108726 1300602 Eye2_m eye weight 2 (mouse) qtl MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20111116 MGI PMID:10102277 1300602 Eye2_m eye weight 2 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10102277 1300603 Cd8ts2_m CD8 T cell subset 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300603 Cd8ts2_m CD8 T cell subset 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300603 Cd8ts2_m CD8 T cell subset 2 (mouse) qtl MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20111116 MGI PMID:12595899 1300604 Mndl1_m mandible length 1 (mouse) qtl MP:0000088 short mandible IAGP N RGD:5509061 20111116 MGI PMID:12161465 1300604 Mndl1_m mandible length 1 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12161465 1300604 Mndl1_m mandible length 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12161465 1300605 El5_m epilepsy 5 (mouse) qtl MP:0002064 seizures IAGP N RGD:5509061 20111116 MGI PMID:8747920 1300605 El5_m epilepsy 5 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8747920 1300605 El5_m epilepsy 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8747920 1300606 Axtofa6_m anxiety-open field activity 6 (mouse) qtl MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20111116 MGI PMID:14990867 1300606 Axtofa6_m anxiety-open field activity 6 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11454769|PMID:14990867 1300606 Axtofa6_m anxiety-open field activity 6 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160422 MGI Created by mouse qtl pipeline PMID:11493566|PMID:11454769 1300607 Tnbs2_m tri-nitrobenzene sulfonic acid susceptible 2 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300607 Tnbs2_m tri-nitrobenzene sulfonic acid susceptible 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300607 Tnbs2_m tri-nitrobenzene sulfonic acid susceptible 2 (mouse) qtl MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20111116 MGI PMID:12145808 1300607 Tnbs2_m tri-nitrobenzene sulfonic acid susceptible 2 (mouse) qtl MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20111116 MGI PMID:12145808 1300611 Tlln_m tail length (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:10051315 1300611 Tlln_m tail length (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:17541685 1300611 Tlln_m tail length (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10051315 1300612 Idd13_m insulin dependent diabetes susceptibility 13 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:7931087 1300612 Idd13_m insulin dependent diabetes susceptibility 13 (mouse) qtl MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20111116 MGI PMID:12759418 1300612 Idd13_m insulin dependent diabetes susceptibility 13 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12759418|PMID:7931087 1300612 Idd13_m insulin dependent diabetes susceptibility 13 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12759418|PMID:7931087 1300612 Idd13_m insulin dependent diabetes susceptibility 13 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:12759418|PMID:7931087 1300612 Idd13_m insulin dependent diabetes susceptibility 13 (mouse) qtl MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20111116 MGI PMID:12759418 1300613 Pcyts4_m plasmacytoma susceptibility 4 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12149518 1300613 Pcyts4_m plasmacytoma susceptibility 4 (mouse) qtl MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20111116 MGI PMID:12149518 1300614 Afw6_m abdominal fat weight QTL 6 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089|PMID:9725853 1300615 Hpic4_m haloperidol induced catalepsy 4 (mouse) qtl MP:0002822 catalepsy IAGP N RGD:5509061 20111116 MGI PMID:10454512 1300615 Hpic4_m haloperidol induced catalepsy 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11166067 1300615 Hpic4_m haloperidol induced catalepsy 4 (mouse) qtl MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20111116 MGI PMID:10454512 1300617 Naq1_m nurturing ability QTL 1 (mouse) qtl MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20111116 MGI PMID:11869186 1300617 Naq1_m nurturing ability QTL 1 (mouse) qtl MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20111116 MGI PMID:15472464 1300617 Naq1_m nurturing ability QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11869186 1300619 Cdcs1_m cytokine deficiency colitis susceptibility 1 (mouse) qtl MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20111116 MGI PMID:11707574 1300619 Cdcs1_m cytokine deficiency colitis susceptibility 1 (mouse) qtl MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20111116 MGI PMID:11707574 1300619 Cdcs1_m cytokine deficiency colitis susceptibility 1 (mouse) qtl MP:0002816 colitis IAGP N RGD:5509061 20150702 MGI PMID:11707574 1300619 Cdcs1_m cytokine deficiency colitis susceptibility 1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11707574 1300619 Cdcs1_m cytokine deficiency colitis susceptibility 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11707574 1300621 Tpnr1_m thermal pain response 1 (mouse) qtl MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20111116 MGI PMID:9150302 1300621 Tpnr1_m thermal pain response 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9150302 1300621 Tpnr1_m thermal pain response 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9150302 1300622 Cfld1_m cystic fibrosis lung disease 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:12461645 1300622 Cfld1_m cystic fibrosis lung disease 1 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12461645 1300622 Cfld1_m cystic fibrosis lung disease 1 (mouse) qtl MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20111116 MGI PMID:12461645 1300624 Insq7_m insulin QTL 7 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:10871196 1300624 Insq7_m insulin QTL 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10871196 1300625 Cosz2_m cocaine seizure 2 (mouse) qtl MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20111116 MGI PMID:10734168 1300625 Cosz2_m cocaine seizure 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10734168 1300625 Cosz2_m cocaine seizure 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10734168 1300626 Idd9.2_m insulin dependent diabetes susceptibility 9.2 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:10933399 1300626 Idd9.2_m insulin dependent diabetes susceptibility 9.2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10933399 1300627 Sluc26_m susceptibility to lung cancer 26 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1300627 Sluc26_m susceptibility to lung cancer 26 (mouse) qtl MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20111116 MGI PMID:11584065 1300627 Sluc26_m susceptibility to lung cancer 26 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1300627 Sluc26_m susceptibility to lung cancer 26 (mouse) qtl MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1300627 Sluc26_m susceptibility to lung cancer 26 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:11584065 1300628 Lgth6_m body length 6 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12185457 1300628 Lgth6_m body length 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:12185457 1300628 Lgth6_m body length 6 (mouse) qtl MP:0010024 increased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:16254318 1300629 Fbgl2_m fasting blood glucose 2 (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:11473059 1300629 Fbgl2_m fasting blood glucose 2 (mouse) qtl MP:0002871 albuminuria IAGP N RGD:5509061 20111116 MGI PMID:15769825 1300629 Fbgl2_m fasting blood glucose 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11473059 1300629 Fbgl2_m fasting blood glucose 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11473059 1300630 Livq3_m percent liver QTL 3 (mouse) qtl MP:0003402 decreased liver weight IAGP N RGD:5509061 20111116 MGI PMID:10353911 1300630 Livq3_m percent liver QTL 3 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1300632 Loca2_m locomotor activity 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14694905 1300632 Loca2_m locomotor activity 2 (mouse) qtl MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:14694905 1300633 Cdcs7_m cytokine deficiency colitis susceptibility 7 (mouse) qtl MP:0001858 intestinal inflammation IAGP N RGD:5509061 20111116 MGI PMID:12213197 1300633 Cdcs7_m cytokine deficiency colitis susceptibility 7 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12213197 1300633 Cdcs7_m cytokine deficiency colitis susceptibility 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12213197 1300634 Sluc25_m susceptibility to lung cancer 25 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1300634 Sluc25_m susceptibility to lung cancer 25 (mouse) qtl MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20111116 MGI PMID:11584065 1300634 Sluc25_m susceptibility to lung cancer 25 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1300634 Sluc25_m susceptibility to lung cancer 25 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:11584065 1300637 Batq2_m brown fat QTL 2 (mouse) qtl MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:10353911 1300637 Batq2_m brown fat QTL 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1300638 Im7_m immunoregulatory 7 (mouse) qtl MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20111116 MGI PMID:8962125 1300638 Im7_m immunoregulatory 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8962125 1300644 Fob3_m F-line obesity QTL 3 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:10602985 1300644 Fob3_m F-line obesity QTL 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10602985 1300645 Alcp1_m alcohol preference locus 1 (mouse) qtl MP:0001425 abnormal alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:8640219 1300645 Alcp1_m alcohol preference locus 1 (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:15547446 1300645 Alcp1_m alcohol preference locus 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10443995|PMID:9880657 1300645 Alcp1_m alcohol preference locus 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:9880657 1300646 Rapop4_m radiation-induced apoptosis 4 (mouse) qtl MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20111116 MGI PMID:9367689 1300646 Rapop4_m radiation-induced apoptosis 4 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9367689 1300647 Nktcn2_m natural killer T cell numbers 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12960309 1300647 Nktcn2_m natural killer T cell numbers 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12960309 1300647 Nktcn2_m natural killer T cell numbers 2 (mouse) qtl MP:0008039 increased NK T cell number IAGP N RGD:5509061 20111116 MGI PMID:12960309 1300648 Dbsty4_m diabesity 4 (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:11042154 1300648 Dbsty4_m diabesity 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11042154 1300650 Bw18_m body weight QTL 18 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11109545 1300650 Bw18_m body weight QTL 18 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:11109545 1300650 Bw18_m body weight QTL 18 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11109545 1300651 Pcyts3_m plasmacytoma susceptibility 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12149518 1300651 Pcyts3_m plasmacytoma susceptibility 3 (mouse) qtl MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20111116 MGI PMID:12149518 1300652 Vmbic9_m ventral midbrain iron content 9 (mouse) qtl MP:0000192 abnormal mineral level IAGP N RGD:5509061 20111116 MGI PMID:16910173 1300652 Vmbic9_m ventral midbrain iron content 9 (mouse) qtl MP:0003952 abnormal copper level IAGP N RGD:5509061 20111116 MGI PMID:16910173 1300652 Vmbic9_m ventral midbrain iron content 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14744041 1300652 Vmbic9_m ventral midbrain iron content 9 (mouse) qtl MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20111116 MGI PMID:16910173 1300653 Imh1_m IgM hypergammaglobulinemia 1 (mouse) qtl MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:6334582 1300653 Imh1_m IgM hypergammaglobulinemia 1 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:6334582 1300653 Imh1_m IgM hypergammaglobulinemia 1 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:7696204 1300653 Imh1_m IgM hypergammaglobulinemia 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6334582 1300653 Imh1_m IgM hypergammaglobulinemia 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:6334582 1300655 Nidds_m non-insulin-dependent diabetes mellitus in SJL (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:10969845 1300655 Nidds_m non-insulin-dependent diabetes mellitus in SJL (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:10969845 1300655 Nidds_m non-insulin-dependent diabetes mellitus in SJL (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:12107726 1300655 Nidds_m non-insulin-dependent diabetes mellitus in SJL (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:12107726 1300655 Nidds_m non-insulin-dependent diabetes mellitus in SJL (mouse) qtl MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:10969845 1300655 Nidds_m non-insulin-dependent diabetes mellitus in SJL (mouse) qtl MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12107726 1300655 Nidds_m non-insulin-dependent diabetes mellitus in SJL (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12107726 1300655 Nidds_m non-insulin-dependent diabetes mellitus in SJL (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12107726 1300655 Nidds_m non-insulin-dependent diabetes mellitus in SJL (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12107726 1300658 Cara1_m carcass ash in high growth mice 1 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:11309659 1300658 Cara1_m carcass ash in high growth mice 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1300659 Pcd8ts1_m p-glycoprotein positive CD8 T cell subset 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300659 Pcd8ts1_m p-glycoprotein positive CD8 T cell subset 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300659 Pcd8ts1_m p-glycoprotein positive CD8 T cell subset 1 (mouse) qtl MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20111116 MGI PMID:12595899 1300663 Start2_m startle response 2 (mouse) qtl MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20111116 MGI PMID:10086232 1300663 Start2_m startle response 2 (mouse) qtl MP:0005377 hearing/vestibular/ear phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10086232 1300663 Start2_m startle response 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10086232 1300665 Pbw2_m pentobarbital withdrawal QTL 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11978849 1300665 Pbw2_m pentobarbital withdrawal QTL 2 (mouse) qtl MP:0009775 increased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:11978849 1300665 Pbw2_m pentobarbital withdrawal QTL 2 (mouse) qtl MP:0009776 decreased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:11978849 1300665 Pbw2_m pentobarbital withdrawal QTL 2 (mouse) qtl MP:0009776 decreased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:15208631 1300667 Lbw4_m lupus NZB x NZW 4 (mouse) qtl MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20111116 MGI PMID:9922399 1300667 Lbw4_m lupus NZB x NZW 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9922399|PMID:12215897 1300667 Lbw4_m lupus NZB x NZW 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:7937857 1300667 Lbw4_m lupus NZB x NZW 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:9922399|PMID:12215897 1300667 Lbw4_m lupus NZB x NZW 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:7937857 1300670 Sluc19_m susceptibility to lung cancer 19 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1300670 Sluc19_m susceptibility to lung cancer 19 (mouse) qtl MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1300672 Hdlq26_m HDL QTL 26 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14993241 1300672 Hdlq26_m HDL QTL 26 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14993241 1300673 Cosz1_m cocaine seizure 1 (mouse) qtl MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20111116 MGI PMID:10734168 1300673 Cosz1_m cocaine seizure 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10734168 1300673 Cosz1_m cocaine seizure 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10734168 1300674 Nidd3n_m non-insulin-dependent diabetes mellitus 3 in NSY (mouse) qtl MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20111116 MGI PMID:10331425 1300674 Nidd3n_m non-insulin-dependent diabetes mellitus 3 in NSY (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10331425 1300675 Laq1_m lupus associated arthritis quantitative trait locus 1 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20111116 MGI PMID:9449705 1300675 Laq1_m lupus associated arthritis quantitative trait locus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9449705 1300676 Prdt2_m prion disease incubation time 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11353827 1300676 Prdt2_m prion disease incubation time 2 (mouse) qtl MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20111116 MGI PMID:11353827 1300677 Bmd9_m bone mineral density 9 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16355279|PMID:11450694 1300677 Bmd9_m bone mineral density 9 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:11450694 1300677 Bmd9_m bone mineral density 9 (mouse) qtl MP:0021186 decreased bone mineral density of vertebrae IAGP N RGD:5509061 20220915 MGI PMID:11450694 1300677 Bmd9_m bone mineral density 9 (mouse) qtl MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20220922 MGI PMID:16355279 1300679 Nociq2_m nociceptive sensitivity inflammatory QTL 2 (mouse) qtl MP:0002735 abnormal chemical nociception IAGP N RGD:5509061 20111116 MGI PMID:11973013 1300679 Nociq2_m nociceptive sensitivity inflammatory QTL 2 (mouse) qtl MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20111116 MGI PMID:11973013 1300679 Nociq2_m nociceptive sensitivity inflammatory QTL 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11973013 1300679 Nociq2_m nociceptive sensitivity inflammatory QTL 2 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11973013 1300685 Scc5_m colon tumor susceptibility 5 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8944029 1300685 Scc5_m colon tumor susceptibility 5 (mouse) qtl MP:0002020 increased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:14562056 1300685 Scc5_m colon tumor susceptibility 5 (mouse) qtl MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8944029 1300685 Scc5_m colon tumor susceptibility 5 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:8944029 1300686 C10bw4_m castaneus 10 week body weight 4 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:11003694 1300686 C10bw4_m castaneus 10 week body weight 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11003694 1300688 Nidd2k_m Nidd2 on KK-A (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:12115031 1300688 Nidd2k_m Nidd2 on KK-A (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:12115031 1300688 Nidd2k_m Nidd2 on KK-A (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115031 1300688 Nidd2k_m Nidd2 on KK-A (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115031 1300688 Nidd2k_m Nidd2 on KK-A (mouse) qtl MP:0006087 increased body mass index IAGP N RGD:5509061 20111116 MGI PMID:12115031 1300689 Dob1_m Dietary obesity 1 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:8000138 1300689 Dob1_m Dietary obesity 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8000138 1300691 Skmw3_m skeletal muscle weight 3 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:14679300 1300691 Skmw3_m skeletal muscle weight 3 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14679300 1300692 Blmpf1_m bleomycin-induced pulmonary fibrosis 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:12140188 1300692 Blmpf1_m bleomycin-induced pulmonary fibrosis 1 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12140188 1300692 Blmpf1_m bleomycin-induced pulmonary fibrosis 1 (mouse) qtl MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20111116 MGI PMID:12140188 1300694 Tmevd7_m Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 7 (mouse) qtl MP:0000921 demyelination IAGP N RGD:5509061 20111116 MGI PMID:12663542 1300694 Tmevd7_m Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 7 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12663542 1300696 Bpq2_m blood pressure QTL 2 (mouse) qtl MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20111116 MGI PMID:11161799 1300696 Bpq2_m blood pressure QTL 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11161799 1300697 Sle2_m systemic lupus erythmatosus susceptibility 2 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:7889410 1300697 Sle2_m systemic lupus erythmatosus susceptibility 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7889410 1300697 Sle2_m systemic lupus erythmatosus susceptibility 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7889410 1300697 Sle2_m systemic lupus erythmatosus susceptibility 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7889410 1300697 Sle2_m systemic lupus erythmatosus susceptibility 2 (mouse) qtl MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20111116 MGI PMID:18607347 1300697 Sle2_m systemic lupus erythmatosus susceptibility 2 (mouse) qtl MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20111116 MGI PMID:18607347 1300700 Sprol1_m spontaneous proliferation 1 (mouse) qtl MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:10384038 1300700 Sprol1_m spontaneous proliferation 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10384038 1300700 Sprol1_m spontaneous proliferation 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10384038 1300701 Cd8ts1_m CD8 T cell subset 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300701 Cd8ts1_m CD8 T cell subset 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300701 Cd8ts1_m CD8 T cell subset 1 (mouse) qtl MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20111116 MGI PMID:12595899 1300702 Fcsa4_m femoral cross-sectional area 4 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12369778 1300702 Fcsa4_m femoral cross-sectional area 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12369778 1300702 Fcsa4_m femoral cross-sectional area 4 (mouse) qtl MP:0008158 increased diameter of femur IAGP N RGD:5509061 20111116 MGI PMID:12369778 1300704 Cia3_m collagen induced arthritis QTL 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10051620|PMID:19234197 1300704 Cia3_m collagen induced arthritis QTL 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10051620|PMID:19234197 1300705 Lipq2_m lipoprotein QTL 2 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14722362 1300705 Lipq2_m lipoprotein QTL 2 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14722362 1300705 Lipq2_m lipoprotein QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14722362 1300708 Pbwm_m pentobarbital withdrawal modifier (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11529278 1300708 Pbwm_m pentobarbital withdrawal modifier (mouse) qtl MP:0009775 increased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:11529278 1300710 Pcd4ts2_m p-glycoprotein positive CD4 T cell subset 2 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12595899 1300710 Pcd4ts2_m p-glycoprotein positive CD4 T cell subset 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300710 Pcd4ts2_m p-glycoprotein positive CD4 T cell subset 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300712 El2_m epilepsy 2 (mouse) qtl MP:0002064 seizures IAGP N RGD:5509061 20111116 MGI PMID:17010098 1300712 El2_m epilepsy 2 (mouse) qtl MP:0002064 seizures IAGP N RGD:5509061 20111116 MGI PMID:1871601 1300712 El2_m epilepsy 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1871601 1300712 El2_m epilepsy 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1871601 1300714 Idd7_m insulin dependent diabetes susceptibility 7 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:7556956 1300714 Idd7_m insulin dependent diabetes susceptibility 7 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:8401590 1300714 Idd7_m insulin dependent diabetes susceptibility 7 (mouse) qtl MP:0005002 abnormal T cell clonal deletion IAGP N RGD:5509061 20111116 MGI PMID:18292549 1300714 Idd7_m insulin dependent diabetes susceptibility 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8401590|PMID:18292549|PMID:7556956 1300714 Idd7_m insulin dependent diabetes susceptibility 7 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8401590|PMID:18292549|PMID:7556956 1300714 Idd7_m insulin dependent diabetes susceptibility 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8401590|PMID:18292549|PMID:7556956 1300714 Idd7_m insulin dependent diabetes susceptibility 7 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8401590|PMID:18292549|PMID:7556956 1300716 Cd4ts4_m CD4 T cell subset 4 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12595899 1300716 Cd4ts4_m CD4 T cell subset 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300716 Cd4ts4_m CD4 T cell subset 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300720 Skl2_m skeletal size (tail length) 2 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:11178736 1300720 Skl2_m skeletal size (tail length) 2 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1300721 Cfbw3_m cystic fibrosis body weight 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:12461646 1300721 Cfbw3_m cystic fibrosis body weight 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12461646 1300722 Sle3_m systemic lupus erythmatosus susceptibility 3 (mouse) qtl MP:0002493 increased IgG level IAGP N RGD:5509061 20111116 MGI PMID:9922399 1300722 Sle3_m systemic lupus erythmatosus susceptibility 3 (mouse) qtl MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:9922399 1300722 Sle3_m systemic lupus erythmatosus susceptibility 3 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:9922399 1300722 Sle3_m systemic lupus erythmatosus susceptibility 3 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10352264 1300722 Sle3_m systemic lupus erythmatosus susceptibility 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10352264 1300722 Sle3_m systemic lupus erythmatosus susceptibility 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10352264 1300722 Sle3_m systemic lupus erythmatosus susceptibility 3 (mouse) qtl MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20111116 MGI PMID:18607347 1300722 Sle3_m systemic lupus erythmatosus susceptibility 3 (mouse) qtl MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20111116 MGI PMID:18607347 1300724 Idd5a_m insulin dependent diabetes susceptibility 5a (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:11016460 1300724 Idd5a_m insulin dependent diabetes susceptibility 5a (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:11723074 1300724 Idd5a_m insulin dependent diabetes susceptibility 5a (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:15210771 1300724 Idd5a_m insulin dependent diabetes susceptibility 5a (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:18056379 1300726 Pitm4_m prion incubation time 4 (mouse) qtl MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20111116 MGI PMID:11404459 1300726 Pitm4_m prion incubation time 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11404459 1300727 Mptp1_m MPTP sensitivity 1 (mouse) qtl MP:0000836 abnormal substantia nigra morphology IAGP N RGD:5509061 20111116 MGI PMID:12591164 1300727 Mptp1_m MPTP sensitivity 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12591164 1300729 Paam2_m progression of autoimmune arthritis in MRL mice 2 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20111116 MGI PMID:11953986 1300729 Paam2_m progression of autoimmune arthritis in MRL mice 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11953986 1300731 Smdq3_m segregation of mitochondrial DNA QTL 3 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12539044 1300731 Smdq3_m segregation of mitochondrial DNA QTL 3 (mouse) qtl MP:0006037 abnormal mitochondrial fission IAGP N RGD:5509061 20111116 MGI PMID:12539044 1300732 Melm2_m melanoma modifier 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11092979 1300732 Melm2_m melanoma modifier 2 (mouse) qtl MP:0009828 increased tumor latency IAGP N RGD:5509061 20111116 MGI PMID:11092979 1300732 Melm2_m melanoma modifier 2 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:11092979 1300732 Melm2_m melanoma modifier 2 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11092979 1300734 Hdlq25_m HDL QTL 25 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14993241 1300734 Hdlq25_m HDL QTL 25 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14993241 1300740 Tne1_m total number errors (mouse) qtl MP:0001405 impaired coordination IAGP N RGD:5509061 20111116 MGI PMID:11529272 1300740 Tne1_m total number errors (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11529272 1300741 Idd17_m insulin dependent diabetes susceptibility 17 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:9257847 1300741 Idd17_m insulin dependent diabetes susceptibility 17 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9257847 1300743 Skull6_m skull morphology 6 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1300743 Skull6_m skull morphology 6 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300743 Skull6_m skull morphology 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300745 Gvhd1_m graft-versus-host disease 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10233703 1300745 Gvhd1_m graft-versus-host disease 1 (mouse) qtl MP:0005672 increased susceptibility to graft versus host disease IAGP N RGD:5509061 20111116 MGI PMID:10233703 1300746 Skl1_m skeletal size (tail length) 1 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:11178736 1300746 Skl1_m skeletal size (tail length) 1 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1300747 Skts2_m skin tumor susceptibility 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7670492 1300747 Skts2_m skin tumor susceptibility 2 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:7670492 1300747 Skts2_m skin tumor susceptibility 2 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7670492 1300752 Ap6q_m alcohol preference 6 QTL (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:11523702 1300752 Ap6q_m alcohol preference 6 QTL (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:9726281 1300752 Ap6q_m alcohol preference 6 QTL (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9726281 1300753 Eae10_m susceptibility to experimental allergic encephalomyelitis 10 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:9712054 1300753 Eae10_m susceptibility to experimental allergic encephalomyelitis 10 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9712054 1300754 Lith4_m lithogenic gene 4 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:16151694 1300754 Lith4_m lithogenic gene 4 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151694 1300755 Wg3_m weight gain in high growth mice 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11309659 1300755 Wg3_m weight gain in high growth mice 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1300756 Pgia16_m proteoglycan induced arthritis 16 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20111116 MGI PMID:11046062 1300756 Pgia16_m proteoglycan induced arthritis 16 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15084914|PMID:11046062 1300756 Pgia16_m proteoglycan induced arthritis 16 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150925 MGI Created by mouse qtl pipeline PMID:11046062 1300757 Cocia9_m cocaine induced activation 9 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12777963 1300757 Cocia9_m cocaine induced activation 9 (mouse) qtl MP:0008911 induced hyperactivity IAGP N RGD:5509061 20220421 MGI PMID:12777963 1300757 Cocia9_m cocaine induced activation 9 (mouse) qtl MP:0020871 abnormal locomotor response to cocaine IAGP N RGD:5509061 20220421 MGI PMID:12777963 1300758 Bomd4_m bone mineral density 4 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:11697792 1300758 Bomd4_m bone mineral density 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11697792 1300759 Geot_m geotaxia (mouse) qtl MP:0001961 abnormal reflex IAGP N RGD:5509061 20111116 MGI PMID:10086232 1300759 Geot_m geotaxia (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10086232 1300760 Nobq1_m New Zealand obese QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18931681|PMID:11151768 1300760 Nobq1_m New Zealand obese QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18931681|PMID:11151768 1300760 Nobq1_m New Zealand obese QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18931681|PMID:11151768 1300766 Skull16_m skull morphology 16 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1300766 Skull16_m skull morphology 16 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300766 Skull16_m skull morphology 16 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300767 Aliq4_m acute lung injury QTL 4 (mouse) qtl MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20111116 MGI PMID:12718980 1300767 Aliq4_m acute lung injury QTL 4 (mouse) qtl MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20111116 MGI PMID:11954676 1300767 Aliq4_m acute lung injury QTL 4 (mouse) qtl MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20111116 MGI PMID:12718980 1300767 Aliq4_m acute lung injury QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11415940 1300769 Pcyts2_m plasmacytoma susceptibility 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12149518 1300769 Pcyts2_m plasmacytoma susceptibility 2 (mouse) qtl MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20111116 MGI PMID:12149518 1300770 Ltsd6_m lung tumor shape-determining 6 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517788 1300770 Ltsd6_m lung tumor shape-determining 6 (mouse) qtl MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20111116 MGI PMID:12517788 1300771 Fob2_m F-line obesity QTL 2 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:10602985 1300771 Fob2_m F-line obesity QTL 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10602985 1300773 Asbb2_m autoimmune susceptibility in C57BL/6J and BALB/c 2 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:11994421 1300773 Asbb2_m autoimmune susceptibility in C57BL/6J and BALB/c 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11994421 1300774 Pgia7_m proteoglycan induced arthritis 7 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:10615997 1300774 Pgia7_m proteoglycan induced arthritis 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10615997|PMID:15084914 1300774 Pgia7_m proteoglycan induced arthritis 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:10615997 1300775 Scpro1_m stem cell proliferation 1 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:10094931 1300775 Scpro1_m stem cell proliferation 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10094931 1300775 Scpro1_m stem cell proliferation 1 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10094931 1300776 Lfp3_m long free running period 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309657 1300776 Lfp3_m long free running period 3 (mouse) qtl MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:11309657 1300777 Chol10_m cholesterol 10 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14872007 1300777 Chol10_m cholesterol 10 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14872007 1300778 Lprm4_m lymphoproliferation modifier 4 (mouse) qtl MP:0000691 enlarged spleen IAGP N RGD:5509061 20111116 MGI PMID:9403730 1300778 Lprm4_m lymphoproliferation modifier 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9403730 1300778 Lprm4_m lymphoproliferation modifier 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9403730 1300778 Lprm4_m lymphoproliferation modifier 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9403730 1300779 Dyscalc4_m dystrophic cardiac calcinosis 4 (mouse) qtl MP:0002838 decreased susceptibility to dystrophic cardiac calcinosis IAGP N RGD:5509061 20111116 MGI PMID:11526197 1300779 Dyscalc4_m dystrophic cardiac calcinosis 4 (mouse) qtl MP:0002839 increased susceptibility to dystrophic cardiac calcinosis IAGP N RGD:5509061 20111116 MGI PMID:11526197 1300779 Dyscalc4_m dystrophic cardiac calcinosis 4 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11526197 1300781 Lith8_m lithogenic gene 8 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:12949731 1300781 Lith8_m lithogenic gene 8 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12949731 1300782 Rear1_m rearing 1 (mouse) qtl MP:0002574 increased vertical activity IAGP N RGD:5509061 20111116 MGI PMID:14694905 1300782 Rear1_m rearing 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14694905 1300784 Prdt3_m prion disease incubation time 3 (mouse) qtl MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20111116 MGI PMID:12481985 1300784 Prdt3_m prion disease incubation time 3 (mouse) qtl MP:0005364 increased susceptibility to prion infection IAGP N RGD:5509061 20111116 MGI PMID:12481985 1300784 Prdt3_m prion disease incubation time 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11353827 1300786 Bw7_m body weight QTL 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089|PMID:9725853 1300787 Cd8mts5_m CD8 memory T cell subset 5 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12595899 1300787 Cd8mts5_m CD8 memory T cell subset 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300787 Cd8mts5_m CD8 memory T cell subset 5 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300787 Cd8mts5_m CD8 memory T cell subset 5 (mouse) qtl MP:0008049 increased memory T cell number IAGP N RGD:5509061 20111116 MGI PMID:12595899 1300788 Cia2_m collagen induced arthritis QTL 2 (mouse) qtl MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20111116 MGI PMID:10051620 1300788 Cia2_m collagen induced arthritis QTL 2 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17082620 1300788 Cia2_m collagen induced arthritis QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11433381|PMID:10051620|PMID:15529344 1300788 Cia2_m collagen induced arthritis QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20140425 MGI Created by mouse qtl pipeline PMID:10051620 1300788 Cia2_m collagen induced arthritis QTL 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11433381|PMID:10051620|PMID:15529344 1300788 Cia2_m collagen induced arthritis QTL 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20140425 MGI Created by mouse qtl pipeline PMID:10051620 1300789 Idd18_m insulin dependent diabetes susceptibility 18 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:9530623 1300789 Idd18_m insulin dependent diabetes susceptibility 18 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9530623 1300790 Pgia6_m proteoglycan induced arthritis 6 (mouse) qtl MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:12794840 1300790 Pgia6_m proteoglycan induced arthritis 6 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:12794840 1300790 Pgia6_m proteoglycan induced arthritis 6 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:10615997 1300790 Pgia6_m proteoglycan induced arthritis 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10615997 1300790 Pgia6_m proteoglycan induced arthritis 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10615997 1300791 Abbp3_m A/J and C57BL/6 blood pressure 3 (mouse) qtl MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20111116 MGI PMID:14612590 1300791 Abbp3_m A/J and C57BL/6 blood pressure 3 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14612590 1300792 Ltsd8_m lung tumor shape-determining 8 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517788 1300792 Ltsd8_m lung tumor shape-determining 8 (mouse) qtl MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20111116 MGI PMID:12517788 1300794 Spha2_m sperm head anomaly 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15020476 1300794 Spha2_m sperm head anomaly 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15020476 1300794 Spha2_m sperm head anomaly 2 (mouse) qtl MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20111116 MGI PMID:15020476 1300795 Stia2_m serum transfer induced arthritis 2 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11489951 1300795 Stia2_m serum transfer induced arthritis 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11489951 1300796 Lmr5_m leishmaniasis resistance 5 (mouse) qtl MP:0001212 skin lesions IAGP N RGD:5509061 20111116 MGI PMID:11196712 1300796 Lmr5_m leishmaniasis resistance 5 (mouse) qtl MP:0002497 increased IgE level IAGP N RGD:5509061 20111116 MGI PMID:11196712 1300796 Lmr5_m leishmaniasis resistance 5 (mouse) qtl MP:0002497 increased IgE level IAGP N RGD:5509061 20111116 MGI PMID:12058253 1300796 Lmr5_m leishmaniasis resistance 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11196712 1300796 Lmr5_m leishmaniasis resistance 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11196712 1300796 Lmr5_m leishmaniasis resistance 5 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:11196712 1300796 Lmr5_m leishmaniasis resistance 5 (mouse) qtl MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20111116 MGI PMID:16511555 1300796 Lmr5_m leishmaniasis resistance 5 (mouse) qtl MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20111116 MGI PMID:11196712 1300796 Lmr5_m leishmaniasis resistance 5 (mouse) qtl MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20111116 MGI PMID:11196712 1300796 Lmr5_m leishmaniasis resistance 5 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11196712 1300797 Sluc22_m susceptibility to lung cancer 22 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1300797 Sluc22_m susceptibility to lung cancer 22 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1300799 Cfld2_m cystic fibrosis lung disease 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:12461645 1300799 Cfld2_m cystic fibrosis lung disease 2 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12461645 1300799 Cfld2_m cystic fibrosis lung disease 2 (mouse) qtl MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20111116 MGI PMID:12461645 1300800 Ses3_m salmonella enteritidis susceptibility 3 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:12058254 1300800 Ses3_m salmonella enteritidis susceptibility 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058254|PMID:15973461 1300800 Ses3_m salmonella enteritidis susceptibility 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20131011 MGI Created by mouse qtl pipeline PMID:15973461|PMID:12058254 1300800 Ses3_m salmonella enteritidis susceptibility 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20151113 MGI Created by mouse qtl pipeline PMID:12058254 1300804 Bw15_m body weight QTL 15 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:11116089 1300804 Bw15_m body weight QTL 15 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089 1300806 Aod4_m autoimmune ovarian dysgenesis 4 (mouse) qtl MP:0004833 ovary atrophy IAGP N RGD:5509061 20111116 MGI PMID:12133995 1300806 Aod4_m autoimmune ovarian dysgenesis 4 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12133995 1300806 Aod4_m autoimmune ovarian dysgenesis 4 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12133995 1300807 Nidd1k_m Nidd1 on KK-A (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:12115031 1300807 Nidd1k_m Nidd1 on KK-A (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115031 1300808 Afw3_m abdominal fat weight QTL 3 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141016 MGI PMID:9725853 1300808 Afw3_m abdominal fat weight QTL 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089|PMID:9725853 1300808 Afw3_m abdominal fat weight QTL 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20141017 MGI Created by mouse qtl pipeline PMID:9725853 1300809 Ccrs2_m corpus callosum hemisphere surface size 2 (mouse) qtl MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20111116 MGI PMID:9804947 1300809 Ccrs2_m corpus callosum hemisphere surface size 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9804947 1300811 Obq3_m obesity QTL 3 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:9268627 1300811 Obq3_m obesity QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9268627 1300812 Oriq1_m ovulation rate QTL 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300814 Artles_m arterial lesions (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:11463718 1300814 Artles_m arterial lesions (mouse) qtl MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:11463718 1300814 Artles_m arterial lesions (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:11463718 1300814 Artles_m arterial lesions (mouse) qtl MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:11463718 1300814 Artles_m arterial lesions (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11463718 1300814 Artles_m arterial lesions (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11463718 1300817 Orgwq6_m organ weight QTL 6 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1300817 Orgwq6_m organ weight QTL 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12118102 1300817 Orgwq6_m organ weight QTL 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1300817 Orgwq6_m organ weight QTL 6 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1300818 Bbaa10_m B.burgdorferi-associated arthritis 10 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11704805 1300818 Bbaa10_m B.burgdorferi-associated arthritis 10 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11704805 1300819 Hpic3_m haloperidol induced catalepsy 3 (mouse) qtl MP:0002822 catalepsy IAGP N RGD:5509061 20111116 MGI PMID:10454512 1300819 Hpic3_m haloperidol induced catalepsy 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11166067 1300819 Hpic3_m haloperidol induced catalepsy 3 (mouse) qtl MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20111116 MGI PMID:10454512 1300821 Lore1_m loss of righting induced by ethanol 1 (mouse) qtl MP:0001523 impaired righting response IAGP N RGD:5509061 20111116 MGI PMID:11964553 1300821 Lore1_m loss of righting induced by ethanol 1 (mouse) qtl MP:0001523 impaired righting response IAGP N RGD:5509061 20111116 MGI PMID:8974320 1300821 Lore1_m loss of righting induced by ethanol 1 (mouse) qtl MP:0002863 improved righting response IAGP N RGD:5509061 20111116 MGI PMID:11964553 1300821 Lore1_m loss of righting induced by ethanol 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8974320 1300821 Lore1_m loss of righting induced by ethanol 1 (mouse) qtl MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20111116 MGI PMID:15365296 1300821 Lore1_m loss of righting induced by ethanol 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8974320 1300821 Lore1_m loss of righting induced by ethanol 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8974320 1300821 Lore1_m loss of righting induced by ethanol 1 (mouse) qtl MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20111116 MGI PMID:11964553 1300822 Esmr_m experimental severe malaria resistance (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:11796577 1300822 Esmr_m experimental severe malaria resistance (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11796577 1300823 Ath9_m atherosclerosis 9 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:11973313 1300823 Ath9_m atherosclerosis 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11973313 1300825 Wg1_m weight gain in high growth mice 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11309659 1300825 Wg1_m weight gain in high growth mice 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1300827 Cora1_m correlation in cytokine production 1 (mouse) qtl MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20111116 MGI PMID:9887350 1300827 Cora1_m correlation in cytokine production 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9887350 1300828 Aod3_m autoimmune ovarian dysgenesis 3 (mouse) qtl MP:0001868 ovary inflammation IAGP N RGD:5509061 20111116 MGI PMID:12133995 1300828 Aod3_m autoimmune ovarian dysgenesis 3 (mouse) qtl MP:0004833 ovary atrophy IAGP N RGD:5509061 20111116 MGI PMID:12133995 1300828 Aod3_m autoimmune ovarian dysgenesis 3 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12133995 1300828 Aod3_m autoimmune ovarian dysgenesis 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12133995 1300828 Aod3_m autoimmune ovarian dysgenesis 3 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12133995 1300830 Bgeq1_m body growth early QTL 1 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:10689807 1300830 Bgeq1_m body growth early QTL 1 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:8846907 1300830 Bgeq1_m body growth early QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8846907 1300835 Mwq1_m molecular weight of quadriceps QTL 1 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:11116089 1300835 Mwq1_m molecular weight of quadriceps QTL 1 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089 1300838 Orgwq3_m organ weight QTL 3 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1300838 Orgwq3_m organ weight QTL 3 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1300838 Orgwq3_m organ weight QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12118102 1300839 Dyscalc2_m dystrophic cardiac calcinosis 2 (mouse) qtl MP:0002838 decreased susceptibility to dystrophic cardiac calcinosis IAGP N RGD:5509061 20111116 MGI PMID:11526197 1300839 Dyscalc2_m dystrophic cardiac calcinosis 2 (mouse) qtl MP:0002839 increased susceptibility to dystrophic cardiac calcinosis IAGP N RGD:5509061 20111116 MGI PMID:11526197 1300839 Dyscalc2_m dystrophic cardiac calcinosis 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11526197 1300840 Cdcs3_m cytokine deficiency colitis susceptibility 3 (mouse) qtl MP:0001858 intestinal inflammation IAGP N RGD:5509061 20111116 MGI PMID:11707574 1300840 Cdcs3_m cytokine deficiency colitis susceptibility 3 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11707574 1300840 Cdcs3_m cytokine deficiency colitis susceptibility 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11707574 1300841 Ssial1_m susceptibility to sialadenitis 1 (mouse) qtl MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20111116 MGI PMID:11937580 1300841 Ssial1_m susceptibility to sialadenitis 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11937580 1300841 Ssial1_m susceptibility to sialadenitis 1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11937580 1300841 Ssial1_m susceptibility to sialadenitis 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11937580 1300841 Ssial1_m susceptibility to sialadenitis 1 (mouse) qtl MP:0005580 periinsulitis IAGP N RGD:5509061 20111116 MGI PMID:1896073 1300842 Sle9_m systematic lupus erythematosus susceptibility 9 (mouse) qtl MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:10693874 1300842 Sle9_m systematic lupus erythematosus susceptibility 9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10693874 1300844 Emo2_m emotionality 2 (mouse) qtl MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20111116 MGI PMID:10556431 1300844 Emo2_m emotionality 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10556431 1300845 Leg1_m longevity extending gene 1 (mouse) qtl MP:0001661 extended life span IAGP N RGD:5509061 20111116 MGI PMID:11568309 1300845 Leg1_m longevity extending gene 1 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11568309 1300847 Par1_m pulmonary adenoma resistance 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20160222 MGI Created by mouse qtl pipeline PMID:8630506 1300847 Par1_m pulmonary adenoma resistance 1 (mouse) qtl MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20160218 MGI PMID:17363568 1300847 Par1_m pulmonary adenoma resistance 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20160222 MGI Created by mouse qtl pipeline PMID:8630506 1300848 Skull13_m skull morphology 13 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1300848 Skull13_m skull morphology 13 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300848 Skull13_m skull morphology 13 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300849 Sles4_m systemic lupus erythmatosus suppressor 4 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:10485648 1300849 Sles4_m systemic lupus erythmatosus suppressor 4 (mouse) qtl MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:10485648 1300849 Sles4_m systemic lupus erythmatosus suppressor 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10485648 1300850 Mwq4_m molecular weight of quadriceps QTL 4 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:11116089 1300850 Mwq4_m molecular weight of quadriceps QTL 4 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089 1300851 Heal4_m wound healing/regeneration 4 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:12682777 1300851 Heal4_m wound healing/regeneration 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12682777 1300852 Lmr14_m leishmaniasis resistance 14 (mouse) qtl MP:0000599 enlarged liver IAGP N RGD:5509061 20111116 MGI PMID:12654824 1300852 Lmr14_m leishmaniasis resistance 14 (mouse) qtl MP:0000691 enlarged spleen IAGP N RGD:5509061 20111116 MGI PMID:12654824 1300852 Lmr14_m leishmaniasis resistance 14 (mouse) qtl MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20111116 MGI PMID:16511555 1300852 Lmr14_m leishmaniasis resistance 14 (mouse) qtl MP:0002497 increased IgE level IAGP N RGD:5509061 20111116 MGI PMID:11196712 1300852 Lmr14_m leishmaniasis resistance 14 (mouse) qtl MP:0002497 increased IgE level IAGP N RGD:5509061 20111116 MGI PMID:12058253 1300852 Lmr14_m leishmaniasis resistance 14 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1300852 Lmr14_m leishmaniasis resistance 14 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1300852 Lmr14_m leishmaniasis resistance 14 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12058253 1300852 Lmr14_m leishmaniasis resistance 14 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1300852 Lmr14_m leishmaniasis resistance 14 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1300852 Lmr14_m leishmaniasis resistance 14 (mouse) qtl MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20111116 MGI PMID:16511555 1300852 Lmr14_m leishmaniasis resistance 14 (mouse) qtl MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20111116 MGI PMID:16511555 1300852 Lmr14_m leishmaniasis resistance 14 (mouse) qtl MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20111116 MGI PMID:16511555 1300852 Lmr14_m leishmaniasis resistance 14 (mouse) qtl MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20111116 MGI PMID:16511555 1300853 Aggr2_m aggression 2 (mouse) qtl MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20111116 MGI PMID:11826145 1300853 Aggr2_m aggression 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11826145 1300854 Lmr3_m leishmaniasis resistance 3 (mouse) qtl MP:0000599 enlarged liver IAGP N RGD:5509061 20111116 MGI PMID:11196712 1300854 Lmr3_m leishmaniasis resistance 3 (mouse) qtl MP:0000691 enlarged spleen IAGP N RGD:5509061 20111116 MGI PMID:11196712 1300854 Lmr3_m leishmaniasis resistance 3 (mouse) qtl MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20111116 MGI PMID:16511555 1300854 Lmr3_m leishmaniasis resistance 3 (mouse) qtl MP:0002497 increased IgE level IAGP N RGD:5509061 20111116 MGI PMID:11196712 1300854 Lmr3_m leishmaniasis resistance 3 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11196712 1300854 Lmr3_m leishmaniasis resistance 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11196712 1300854 Lmr3_m leishmaniasis resistance 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:11196712 1300854 Lmr3_m leishmaniasis resistance 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11196712 1300854 Lmr3_m leishmaniasis resistance 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11196712 1300854 Lmr3_m leishmaniasis resistance 3 (mouse) qtl MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20111116 MGI PMID:16511555 1300854 Lmr3_m leishmaniasis resistance 3 (mouse) qtl MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20111116 MGI PMID:11196712 1300856 Nobq2_m New Zealand obese QTL 2 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:11151768 1300856 Nobq2_m New Zealand obese QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11151768 1300858 Tafat_m tally ho associated mesenteric fat pad weight (mouse) qtl MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11414755 1300858 Tafat_m tally ho associated mesenteric fat pad weight (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11414755 1300859 Skull8_m skull morphology 8 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1300859 Skull8_m skull morphology 8 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300859 Skull8_m skull morphology 8 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300861 Bfq1_m body fat QTL 1 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:9276742 1300861 Bfq1_m body fat QTL 1 (mouse) qtl MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:9276742 1300861 Bfq1_m body fat QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9276742 1300861 Bfq1_m body fat QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9276742 1300861 Bfq1_m body fat QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9276742 1300861 Bfq1_m body fat QTL 1 (mouse) qtl MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:9276742 1300861 Bfq1_m body fat QTL 1 (mouse) qtl MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:9276742 1300862 Cfbw5_m cystic fibrosis body weight 5 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:12461646 1300862 Cfbw5_m cystic fibrosis body weight 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12461646 1300863 Ltsd4_m lung tumor shape-determining 4 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517788 1300863 Ltsd4_m lung tumor shape-determining 4 (mouse) qtl MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20111116 MGI PMID:12517788 1300864 Eae25_m susceptibility to experimental allergic encephalomyelitis 25 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10706738 1300864 Eae25_m susceptibility to experimental allergic encephalomyelitis 25 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10706738 1300864 Eae25_m susceptibility to experimental allergic encephalomyelitis 25 (mouse) qtl MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20111116 MGI PMID:10706738 1300864 Eae25_m susceptibility to experimental allergic encephalomyelitis 25 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10706738 1300867 Lore2_m loss of righting induced by ethanol 2 (mouse) qtl MP:0001523 impaired righting response IAGP N RGD:5509061 20111116 MGI PMID:11964553 1300867 Lore2_m loss of righting induced by ethanol 2 (mouse) qtl MP:0001523 impaired righting response IAGP N RGD:5509061 20111116 MGI PMID:9880661 1300867 Lore2_m loss of righting induced by ethanol 2 (mouse) qtl MP:0002863 improved righting response IAGP N RGD:5509061 20111116 MGI PMID:11964553 1300867 Lore2_m loss of righting induced by ethanol 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9880661 1300867 Lore2_m loss of righting induced by ethanol 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9880661 1300867 Lore2_m loss of righting induced by ethanol 2 (mouse) qtl MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20111116 MGI PMID:11964553 1300868 Tlf_m T lymphocyte fraction (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9754812 1300868 Tlf_m T lymphocyte fraction (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9754812 1300868 Tlf_m T lymphocyte fraction (mouse) qtl MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20111116 MGI PMID:9754812 1300869 Stheal5_m soft tissue heal 5 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:11731492 1300869 Stheal5_m soft tissue heal 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11731492 1300870 Ath18_m atherosclerosis 18 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:14592847 1300870 Ath18_m atherosclerosis 18 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592847 1300871 Mob5_m multigenic obesity 5 (mouse) qtl MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16873689 1300871 Mob5_m multigenic obesity 5 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16873689 1300871 Mob5_m multigenic obesity 5 (mouse) qtl MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:9616220 1300871 Mob5_m multigenic obesity 5 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:16873689 1300871 Mob5_m multigenic obesity 5 (mouse) qtl MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:16873689 1300871 Mob5_m multigenic obesity 5 (mouse) qtl MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20111116 MGI PMID:16873689 1300871 Mob5_m multigenic obesity 5 (mouse) qtl MP:0005144 abnormal circulating VLDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16873689 1300871 Mob5_m multigenic obesity 5 (mouse) qtl MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16873689 1300871 Mob5_m multigenic obesity 5 (mouse) qtl MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:16873689 1300871 Mob5_m multigenic obesity 5 (mouse) qtl MP:0011582 decreased triglyceride lipase activity IAGP N RGD:5509061 20120209 MGI PMID:9616220 1300871 Mob5_m multigenic obesity 5 (mouse) qtl MP:0011939 increased food intake IAGP N RGD:5509061 20130517 MGI PMID:16873689 1300872 Afpq2_m abdominal fat percent QTL 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089|PMID:9725853 1300874 Gasa2_m gastritis type A susceptibility locus 2 (mouse) qtl MP:0001873 stomach inflammation IAGP N RGD:5509061 20111116 MGI PMID:10227980 1300874 Gasa2_m gastritis type A susceptibility locus 2 (mouse) qtl MP:0001873 stomach inflammation IAGP N RGD:5509061 20111116 MGI PMID:11862406 1300874 Gasa2_m gastritis type A susceptibility locus 2 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10227980 1300874 Gasa2_m gastritis type A susceptibility locus 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10227980 1300876 Tanidd2_m tally ho associated non-insulin dependednt diabetes mellitus 2 (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:11414755 1300876 Tanidd2_m tally ho associated non-insulin dependednt diabetes mellitus 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11414755 1300877 Adip8_m adiposity 8 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11178736 1300877 Adip8_m adiposity 8 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1300878 Skts1_m skin tumor susceptibility 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309660|PMID:7670492 1300878 Skts1_m skin tumor susceptibility 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20150703 MGI Created by mouse qtl pipeline PMID:7670492 1300878 Skts1_m skin tumor susceptibility 1 (mouse) qtl MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:7670492 1300878 Skts1_m skin tumor susceptibility 1 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:7670492 1300878 Skts1_m skin tumor susceptibility 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309660|PMID:7670492 1300878 Skts1_m skin tumor susceptibility 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20150703 MGI Created by mouse qtl pipeline PMID:7670492 1300879 Sle1b_m systematic lupus erythematosus susceptibility 1b (mouse) qtl MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20111116 MGI PMID:11172029 1300879 Sle1b_m systematic lupus erythematosus susceptibility 1b (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11172029 1300881 Sluc29_m susceptibility to lung cancer 29 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1300881 Sluc29_m susceptibility to lung cancer 29 (mouse) qtl MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1300882 Ath17_m atherosclerosis 17 (mouse) qtl MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:14592847 1300882 Ath17_m atherosclerosis 17 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592847 1300883 Ath21_m atherosclerosis 21 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:14592847 1300883 Ath21_m atherosclerosis 21 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592847 1300885 Mbis4_m Mycobacterium bovis-induced systemic lupus erythematosus 4 (mouse) qtl MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:10903779 1300885 Mbis4_m Mycobacterium bovis-induced systemic lupus erythematosus 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10903779 1300887 Pabr1_m plasma apolipoprotein B (human) regulator 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11352992 1300887 Pabr1_m plasma apolipoprotein B (human) regulator 1 (mouse) qtl MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20111116 MGI PMID:11352992 1300888 Berr1_m berghei resistance locus 1 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:12114535 1300888 Berr1_m berghei resistance locus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12114535 1300889 Lith9_m lithogenic gene 9 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:12949731 1300889 Lith9_m lithogenic gene 9 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:16151694 1300889 Lith9_m lithogenic gene 9 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151694|PMID:12949731 1300889 Lith9_m lithogenic gene 9 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20150724 MGI Created by mouse qtl pipeline PMID:12949731 1300890 Bhr3_m bronchial hyperresponsiveness 3 (mouse) qtl MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20111116 MGI PMID:7550342 1300890 Bhr3_m bronchial hyperresponsiveness 3 (mouse) qtl MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20111116 MGI PMID:7550342 1300890 Bhr3_m bronchial hyperresponsiveness 3 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7550342 1300891 Obq8_m obesity QTL 8 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11210195 1300891 Obq8_m obesity QTL 8 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11210195 1300892 Szs10_m seizure susceptibility 10 (mouse) qtl MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20111116 MGI PMID:11472065 1300892 Szs10_m seizure susceptibility 10 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1300892 Szs10_m seizure susceptibility 10 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1300894 Capop_m cyclophosphamide induced apoptosis (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11247636 1300894 Capop_m cyclophosphamide induced apoptosis (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11247636 1300894 Capop_m cyclophosphamide induced apoptosis (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:11247636 1300894 Capop_m cyclophosphamide induced apoptosis (mouse) qtl MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20111116 MGI PMID:11247636 1300895 Hdl5_m HDL level 5 (mouse) qtl MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12925895 1300895 Hdl5_m HDL level 5 (mouse) qtl MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18048852 1300895 Hdl5_m HDL level 5 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12925895 1300895 Hdl5_m HDL level 5 (mouse) qtl MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18048852 1300895 Hdl5_m HDL level 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18048852|PMID:12925895 1300895 Hdl5_m HDL level 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:12925895 1300897 Cocia12_m cocaine induced activation 12 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12777963 1300897 Cocia12_m cocaine induced activation 12 (mouse) qtl MP:0008911 induced hyperactivity IAGP N RGD:5509061 20220421 MGI PMID:12777963 1300897 Cocia12_m cocaine induced activation 12 (mouse) qtl MP:0020871 abnormal locomotor response to cocaine IAGP N RGD:5509061 20220421 MGI PMID:12777963 1300898 Cfid_m cystic fibrosis intestinal distress (mouse) qtl MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20111116 MGI PMID:12441405 1300898 Cfid_m cystic fibrosis intestinal distress (mouse) qtl MP:0002083 premature death IAGP N RGD:5509061 20111116 MGI PMID:12441405 1300898 Cfid_m cystic fibrosis intestinal distress (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12441405 1300898 Cfid_m cystic fibrosis intestinal distress (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12441405 1300899 Chol6_m cholesterol 6 (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12588951 1300899 Chol6_m cholesterol 6 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12588951 1300899 Chol6_m cholesterol 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12588951 1300901 Skts10_m skin tumor susceptibility 10 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1300901 Skts10_m skin tumor susceptibility 10 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:10611333 1300901 Skts10_m skin tumor susceptibility 10 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1300902 Hdl3_m high density lipoprotein (HDL) level 3 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:11108726 1300902 Hdl3_m high density lipoprotein (HDL) level 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11108726 1300904 Chab5_m cholesterol absorption 5 (mouse) qtl MP:0002646 increased intestinal cholesterol absorption IAGP N RGD:5509061 20111116 MGI PMID:11714849 1300904 Chab5_m cholesterol absorption 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11714849 1300904 Chab5_m cholesterol absorption 5 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11714849 1300905 Scc6_m colon tumor susceptibility 6 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10485458 1300905 Scc6_m colon tumor susceptibility 6 (mouse) qtl MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20111116 MGI PMID:10485458 1300905 Scc6_m colon tumor susceptibility 6 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:10485458 1300906 Ap8q_m alcohol preference 8 QTL (mouse) qtl MP:0001425 abnormal alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:12176933 1300906 Ap8q_m alcohol preference 8 QTL (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:12176933 1300906 Ap8q_m alcohol preference 8 QTL (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12176933 1300908 Insq4_m insulin QTL 4 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:11109545 1300908 Insq4_m insulin QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11109545 1300909 Ath13_m atherosclerosis 13 (mouse) qtl MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20111116 MGI PMID:11973313 1300909 Ath13_m atherosclerosis 13 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11973313 1300911 Idd19_m insulin dependent diabetes susceptibility 19 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:11386752 1300911 Idd19_m insulin dependent diabetes susceptibility 19 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:9647636 1300911 Idd19_m insulin dependent diabetes susceptibility 19 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11386752|PMID:9647636 1300913 Bwefm_m body weight females and males day 10 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:10086232 1300913 Bwefm_m body weight females and males day 10 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10086232 1300915 Lmr12_m leishmaniasis resistance 12 (mouse) qtl MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20111116 MGI PMID:16511555 1300915 Lmr12_m leishmaniasis resistance 12 (mouse) qtl MP:0002492 decreased IgE level IAGP N RGD:5509061 20111116 MGI PMID:12058253 1300915 Lmr12_m leishmaniasis resistance 12 (mouse) qtl MP:0002497 increased IgE level IAGP N RGD:5509061 20111116 MGI PMID:12058253 1300915 Lmr12_m leishmaniasis resistance 12 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1300915 Lmr12_m leishmaniasis resistance 12 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12058253 1300915 Lmr12_m leishmaniasis resistance 12 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1300915 Lmr12_m leishmaniasis resistance 12 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1300915 Lmr12_m leishmaniasis resistance 12 (mouse) qtl MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20111116 MGI PMID:16511555 1300915 Lmr12_m leishmaniasis resistance 12 (mouse) qtl MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20111116 MGI PMID:16511555 1300916 Mobe2_m modifier of obesity 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:14693723 1300916 Mobe2_m modifier of obesity 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14693723 1300917 Gasa1_m gastritis type A susceptibility locus 1 (mouse) qtl MP:0001873 stomach inflammation IAGP N RGD:5509061 20111116 MGI PMID:10227980 1300917 Gasa1_m gastritis type A susceptibility locus 1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10227980 1300917 Gasa1_m gastritis type A susceptibility locus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10227980 1300918 Stheal4_m soft tissue heal 4 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:11731492 1300918 Stheal4_m soft tissue heal 4 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:16341671 1300918 Stheal4_m soft tissue heal 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16341671|PMID:11731492 1300918 Stheal4_m soft tissue heal 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:11731492 1300919 Nidd2_m non-insulin-dependent diabetes mellitus 2 (mouse) qtl MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:9703330 1300919 Nidd2_m non-insulin-dependent diabetes mellitus 2 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:9703330 1300919 Nidd2_m non-insulin-dependent diabetes mellitus 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9703330 1300920 Pitm3_m prion incubation time 3 (mouse) qtl MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20111116 MGI PMID:11404459 1300920 Pitm3_m prion incubation time 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11404459 1300921 Skl4_m skeletal size (tail length) 4 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:11178736 1300921 Skl4_m skeletal size (tail length) 4 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1300922 Actd1_m activity-distance traveled 1 (mouse) qtl MP:0001399 hyperactivity IAGP N RGD:5509061 20111116 MGI PMID:11105390 1300922 Actd1_m activity-distance traveled 1 (mouse) qtl MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20111116 MGI PMID:11105390 1300922 Actd1_m activity-distance traveled 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11105390 1300923 Bits4_m bitterness sensitivity 4 (mouse) qtl MP:0004210 abnormal bitter taste sensitivity IAGP N RGD:5509061 20111116 MGI PMID:10609087 1300923 Bits4_m bitterness sensitivity 4 (mouse) qtl MP:0005394 taste/olfaction phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10609087 1300924 Ity2_m immunity to S. typhimurium 2 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:9479490 1300924 Ity2_m immunity to S. typhimurium 2 (mouse) qtl MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:17660555 1300924 Ity2_m immunity to S. typhimurium 2 (mouse) qtl MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:9479490 1300924 Ity2_m immunity to S. typhimurium 2 (mouse) qtl MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20111116 MGI PMID:16688529 1300924 Ity2_m immunity to S. typhimurium 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9479490 1300925 Lbm4_m lean body mass 4 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:12185457 1300925 Lbm4_m lean body mass 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12185457 1300926 Hpi2_m hepatic PMN infiltration 2 (mouse) qtl MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11053246 1300926 Hpi2_m hepatic PMN infiltration 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11053246 1300929 Pcyts1_m plasmacytoma susceptibility 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12149518 1300929 Pcyts1_m plasmacytoma susceptibility 1 (mouse) qtl MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20111116 MGI PMID:12149518 1300932 Hdlq17_m HDL QTL 17 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14592847 1300932 Hdlq17_m HDL QTL 17 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14872007 1300932 Hdlq17_m HDL QTL 17 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592847|PMID:14872007 1300932 Hdlq17_m HDL QTL 17 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:14592847 1300933 Cdcs9_m cytokine deficiency colitis susceptibility 9 (mouse) qtl MP:0001858 intestinal inflammation IAGP N RGD:5509061 20111116 MGI PMID:12213197 1300933 Cdcs9_m cytokine deficiency colitis susceptibility 9 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12213197 1300933 Cdcs9_m cytokine deficiency colitis susceptibility 9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12213197 1300934 Cfbw1_m cystic fibrosis body weight 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:12461646 1300934 Cfbw1_m cystic fibrosis body weight 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12461646 1300936 Dloc2_m duration of locomotor activity 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14694905 1300936 Dloc2_m duration of locomotor activity 2 (mouse) qtl MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:14694905 1300938 Bulb3_m bulb size 3 (mouse) qtl MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20111116 MGI PMID:11529276 1300938 Bulb3_m bulb size 3 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11529276 1300939 Hrtfm6_m heart failure modifier 6 (mouse) qtl MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20111116 MGI PMID:14519689 1300939 Hrtfm6_m heart failure modifier 6 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14519689 1300939 Hrtfm6_m heart failure modifier 6 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14519689 1300940 Actd3_m activity-distance traveled 3 (mouse) qtl MP:0001399 hyperactivity IAGP N RGD:5509061 20111116 MGI PMID:11105390 1300940 Actd3_m activity-distance traveled 3 (mouse) qtl MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20111116 MGI PMID:11105390 1300940 Actd3_m activity-distance traveled 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11105390 1300941 Skl6_m skeletal size (tail length) 6 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:11178736 1300941 Skl6_m skeletal size (tail length) 6 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1300943 Skts9_m skin tumor susceptibility 9 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1300943 Skts9_m skin tumor susceptibility 9 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:10611333 1300943 Skts9_m skin tumor susceptibility 9 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1300945 Bglq7_m body growth late QTL 7 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:8846907 1300945 Bglq7_m body growth late QTL 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8846907 1300946 Sle1c_m systematic lupus erythematosus susceptibility 1c (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:17372026 1300946 Sle1c_m systematic lupus erythematosus susceptibility 1c (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:17372026 1300946 Sle1c_m systematic lupus erythematosus susceptibility 1c (mouse) qtl MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20111116 MGI PMID:11172029 1300946 Sle1c_m systematic lupus erythematosus susceptibility 1c (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11172029|PMID:17372026 1300946 Sle1c_m systematic lupus erythematosus susceptibility 1c (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11172029|PMID:17372026 1300946 Sle1c_m systematic lupus erythematosus susceptibility 1c (mouse) qtl MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:17372026 1300948 Fglu2_m fasting glucose 2 (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:12439655 1300948 Fglu2_m fasting glucose 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12439655 1300949 Lore5_m loss of righting induced by ethanol 5 (mouse) qtl MP:0001523 impaired righting response IAGP N RGD:5509061 20111116 MGI PMID:11964553 1300949 Lore5_m loss of righting induced by ethanol 5 (mouse) qtl MP:0002863 improved righting response IAGP N RGD:5509061 20111116 MGI PMID:11964553 1300949 Lore5_m loss of righting induced by ethanol 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11964553 1300951 Gbvq1_m gallstone bladder volume QTL 1 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12837957 1300951 Gbvq1_m gallstone bladder volume QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12837957 1300951 Gbvq1_m gallstone bladder volume QTL 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12837957 1300951 Gbvq1_m gallstone bladder volume QTL 1 (mouse) qtl MP:0020132 increased gallbladder volume IAGP N RGD:5509061 20200116 MGI PMID:12837957 1300952 Hcs1_m hepatocarcinogenesis susceptibility 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8417808 1300952 Hcs1_m hepatocarcinogenesis susceptibility 1 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:8417808 1300952 Hcs1_m hepatocarcinogenesis susceptibility 1 (mouse) qtl MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8417808 1300954 Fcsa1_m femoral cross-sectional area 1 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12369778 1300954 Fcsa1_m femoral cross-sectional area 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12369778 1300954 Fcsa1_m femoral cross-sectional area 1 (mouse) qtl MP:0008158 increased diameter of femur IAGP N RGD:5509061 20111116 MGI PMID:12369778 1300955 Pcpila2_m PCP induced locomotor activity 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8914121 1300955 Pcpila2_m PCP induced locomotor activity 2 (mouse) qtl MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20111116 MGI PMID:8914121 1300956 Sle15_m systematic lupus erythematosus susceptibility 15 (mouse) qtl MP:0002493 increased IgG level IAGP N RGD:5509061 20111116 MGI PMID:15034079 1300956 Sle15_m systematic lupus erythematosus susceptibility 15 (mouse) qtl MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:15034079 1300956 Sle15_m systematic lupus erythematosus susceptibility 15 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:15034079 1300956 Sle15_m systematic lupus erythematosus susceptibility 15 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:15034079 1300956 Sle15_m systematic lupus erythematosus susceptibility 15 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:15034079 1300957 Pbd1_m peak bone density 1 (mouse) qtl MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20111116 MGI PMID:9922384 1300957 Pbd1_m peak bone density 1 (mouse) qtl MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20111116 MGI PMID:17295603 1300957 Pbd1_m peak bone density 1 (mouse) qtl MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20111116 MGI PMID:9922384 1300957 Pbd1_m peak bone density 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9922384 1300959 Lxw2_m lupus BXSB x NZW 2 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:14662843 1300959 Lxw2_m lupus BXSB x NZW 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14662843 1300959 Lxw2_m lupus BXSB x NZW 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14662843 1300960 Hpic2_m haloperidol induced catalepsy 2 (mouse) qtl MP:0002822 catalepsy IAGP N RGD:5509061 20111116 MGI PMID:10765558 1300960 Hpic2_m haloperidol induced catalepsy 2 (mouse) qtl MP:0002822 catalepsy IAGP N RGD:5509061 20111116 MGI PMID:17696997 1300960 Hpic2_m haloperidol induced catalepsy 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10765558 1300961 Bh4p_m bar holding four paws (mouse) qtl MP:0004262 abnormal physical strength IAGP N RGD:5509061 20111116 MGI PMID:10086232 1300961 Bh4p_m bar holding four paws (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10086232 1300962 Cd8mts4_m CD8 memory T cell subset 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300962 Cd8mts4_m CD8 memory T cell subset 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1300962 Cd8mts4_m CD8 memory T cell subset 4 (mouse) qtl MP:0008049 increased memory T cell number IAGP N RGD:5509061 20111116 MGI PMID:12595899 1300963 Hrl_m herpes resistance locus (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14557652 1300963 Hrl_m herpes resistance locus (mouse) qtl MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:14557652 1300964 Hdlq22_m HDL QTL 22 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14993241 1300964 Hdlq22_m HDL QTL 22 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14993241 1300966 Pabr2_m plasma apolipoprotein B (human) regulator 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11352992 1300966 Pabr2_m plasma apolipoprotein B (human) regulator 2 (mouse) qtl MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20111116 MGI PMID:11352992 1300968 Skts4_m skin tumor susceptibility 4 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9667751 1300968 Skts4_m skin tumor susceptibility 4 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:9667751 1300968 Skts4_m skin tumor susceptibility 4 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9667751 1300969 Sluc5_m susceptibility to lung cancer 5 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9809979 1300969 Sluc5_m susceptibility to lung cancer 5 (mouse) qtl MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20111116 MGI PMID:11584065 1300969 Sluc5_m susceptibility to lung cancer 5 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1300969 Sluc5_m susceptibility to lung cancer 5 (mouse) qtl MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1300969 Sluc5_m susceptibility to lung cancer 5 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9809979 1300970 Cdcs4_m cytokine deficiency colitis susceptibility 4 (mouse) qtl MP:0001858 intestinal inflammation IAGP N RGD:5509061 20111116 MGI PMID:11707574 1300970 Cdcs4_m cytokine deficiency colitis susceptibility 4 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11707574 1300970 Cdcs4_m cytokine deficiency colitis susceptibility 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11707574 1300971 Pgia14_m proteoglycan induced arthritis 14 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:11046062 1300971 Pgia14_m proteoglycan induced arthritis 14 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11046062 1300971 Pgia14_m proteoglycan induced arthritis 14 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11046062 1300972 Cocia11_m cocaine induced activation 11 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12777963 1300972 Cocia11_m cocaine induced activation 11 (mouse) qtl MP:0008911 induced hyperactivity IAGP N RGD:5509061 20220421 MGI PMID:12777963 1300972 Cocia11_m cocaine induced activation 11 (mouse) qtl MP:0020871 abnormal locomotor response to cocaine IAGP N RGD:5509061 20220421 MGI PMID:12777963 1300973 Abmm_m antibody mediated myocarditis (mouse) qtl MP:0001856 myocarditis IAGP N RGD:5509061 20111116 MGI PMID:9887344 1300973 Abmm_m antibody mediated myocarditis (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9887344 1300973 Abmm_m antibody mediated myocarditis (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9887344 1300974 Pgia9_m proteoglycan induced arthritis 9 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10615997 1300974 Pgia9_m proteoglycan induced arthritis 9 (mouse) qtl MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:18606685 1300974 Pgia9_m proteoglycan induced arthritis 9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18606685|PMID:10615997|PMID:15084914 1300974 Pgia9_m proteoglycan induced arthritis 9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150925 MGI Created by mouse qtl pipeline PMID:18606685|PMID:10615997 1300974 Pgia9_m proteoglycan induced arthritis 9 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18606685|PMID:10615997|PMID:15084914 1300974 Pgia9_m proteoglycan induced arthritis 9 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20150925 MGI Created by mouse qtl pipeline PMID:18606685|PMID:10615997 1300974 Pgia9_m proteoglycan induced arthritis 9 (mouse) qtl MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20111116 MGI PMID:18606685 1300974 Pgia9_m proteoglycan induced arthritis 9 (mouse) qtl MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20111116 MGI PMID:18606685 1300975 Fembrs3_m femur breaking strength 3 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:11991724 1300975 Fembrs3_m femur breaking strength 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11991724 1300976 Bmd19_m bone mineral density 19 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12568393 1300976 Bmd19_m bone mineral density 19 (mouse) qtl MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:12568393 1300977 Mopkd1_m modifier of polycystic kidney disease progression 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9329956 1300977 Mopkd1_m modifier of polycystic kidney disease progression 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9329956 1300977 Mopkd1_m modifier of polycystic kidney disease progression 1 (mouse) qtl MP:0008528 polycystic kidney IAGP N RGD:5509061 20111116 MGI PMID:9329956 1300979 Sbmd3_m spinal bone mineral density 3 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:10780854 1300979 Sbmd3_m spinal bone mineral density 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10780854 1300982 Lmr11_m leishmaniasis resistance 11 (mouse) qtl MP:0002492 decreased IgE level IAGP N RGD:5509061 20111116 MGI PMID:12058253 1300982 Lmr11_m leishmaniasis resistance 11 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1300982 Lmr11_m leishmaniasis resistance 11 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1300982 Lmr11_m leishmaniasis resistance 11 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:12058253 1300982 Lmr11_m leishmaniasis resistance 11 (mouse) qtl MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20111116 MGI PMID:16511555 1300984 Start1_m startle response 1 (mouse) qtl MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20111116 MGI PMID:10086232 1300984 Start1_m startle response 1 (mouse) qtl MP:0005377 hearing/vestibular/ear phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10086232 1300984 Start1_m startle response 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10086232 1300985 Bmd13_m bone mineral density 13 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:11450694 1300985 Bmd13_m bone mineral density 13 (mouse) qtl MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20111116 MGI PMID:17371164 1300985 Bmd13_m bone mineral density 13 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11450694|PMID:12568393 1300986 Hdlq2_m HDL QTL 2 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12006675 1300986 Hdlq2_m HDL QTL 2 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14993241 1300986 Hdlq2_m HDL QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12006675 1300987 Skull23_m skull morphology 23 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1300987 Skull23_m skull morphology 23 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300987 Skull23_m skull morphology 23 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1300989 Lrdg1_m light induced retinal degeneration 1 (mouse) qtl MP:0001326 retina degeneration IAGP N RGD:5509061 20111116 MGI PMID:15112105 1300989 Lrdg1_m light induced retinal degeneration 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15112105 1300990 Bits3_m bitterness sensitivity 3 (mouse) qtl MP:0004210 abnormal bitter taste sensitivity IAGP N RGD:5509061 20111116 MGI PMID:10609087 1300990 Bits3_m bitterness sensitivity 3 (mouse) qtl MP:0005394 taste/olfaction phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10609087 1300991 Cpfd4_m cerebellum pattern fissures (mouse) qtl MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20111116 MGI PMID:11529272 1300991 Cpfd4_m cerebellum pattern fissures (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11529272 1300992 Cocia14_m cocaine induced activation 14 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12777963 1300992 Cocia14_m cocaine induced activation 14 (mouse) qtl MP:0008911 induced hyperactivity IAGP N RGD:5509061 20220421 MGI PMID:12777963 1300992 Cocia14_m cocaine induced activation 14 (mouse) qtl MP:0020871 abnormal locomotor response to cocaine IAGP N RGD:5509061 20220421 MGI PMID:12777963 1300995 Fembrs4_m femur breaking strength 4 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:11991724 1300995 Fembrs4_m femur breaking strength 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11991724 1300996 Aorls2_m aortic lesion size 2 (mouse) qtl MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20111116 MGI PMID:12925895 1300996 Aorls2_m aortic lesion size 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12925895 1300997 Eae15_m susceptibility to experimental allergic encephalomyelitis 15 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10934166 1300997 Eae15_m susceptibility to experimental allergic encephalomyelitis 15 (mouse) qtl MP:0021002 brain lesion IAGP N RGD:5509061 20210805 MGI PMID:10934166 1300999 Carp1_m carcass protein in high growth mice 1 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:11309659 1300999 Carp1_m carcass protein in high growth mice 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301000 Obq5_m obesity QTL 5 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:10501964 1301000 Obq5_m obesity QTL 5 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10501964 1301003 Lmblgq4_m limb length QTL 4 (mouse) qtl MP:0002764 short tibia IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301003 Lmblgq4_m limb length QTL 4 (mouse) qtl MP:0003109 short femur IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301003 Lmblgq4_m limb length QTL 4 (mouse) qtl MP:0004351 short humerus IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301003 Lmblgq4_m limb length QTL 4 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301003 Lmblgq4_m limb length QTL 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301004 Hdlq27_m HDL QTL 27 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14993241 1301004 Hdlq27_m HDL QTL 27 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14993241 1301005 Idd16_m insulin dependent diabetes susceptibility 16 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:12086944 1301005 Idd16_m insulin dependent diabetes susceptibility 16 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:14513297 1301005 Idd16_m insulin dependent diabetes susceptibility 16 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:15561967 1301005 Idd16_m insulin dependent diabetes susceptibility 16 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14513297|PMID:15561967 1301006 Hfib1_m hepatic fibrogenesis 1 (mouse) qtl MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20111116 MGI PMID:12454860 1301006 Hfib1_m hepatic fibrogenesis 1 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12454860 1301007 Pid2_m prion incubation determinant 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11013074 1301007 Pid2_m prion incubation determinant 2 (mouse) qtl MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20111116 MGI PMID:11013074 1301009 Pbwg7_m postnatal body weight growth 7 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 1301009 Pbwg7_m postnatal body weight growth 7 (mouse) qtl MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20111116 MGI PMID:15056934 1301009 Pbwg7_m postnatal body weight growth 7 (mouse) qtl MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20111116 MGI PMID:16174331 1301009 Pbwg7_m postnatal body weight growth 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15056934 1301010 ahl2_m age related hearing loss 2 (mouse) qtl MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20111116 MGI PMID:12408962 1301010 ahl2_m age related hearing loss 2 (mouse) qtl MP:0005377 hearing/vestibular/ear phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12408962 1301012 Vispl_m visual placing (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10086232 1301013 Capsq4_m capsaicin sensitivity related QTL 4 (mouse) qtl MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20111116 MGI PMID:14499433 1301013 Capsq4_m capsaicin sensitivity related QTL 4 (mouse) qtl MP:0005394 taste/olfaction phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14499433 1301014 Dob7_m dietary obesity 7 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:9321464 1301014 Dob7_m dietary obesity 7 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:9321464 1301014 Dob7_m dietary obesity 7 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9321464 1301014 Dob7_m dietary obesity 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9321464 1301015 Sysbp2_m systolic blood pressure 2 (mouse) qtl MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20111116 MGI PMID:10523337 1301015 Sysbp2_m systolic blood pressure 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10523337 1301016 Szs1_m seizure susceptibility 1 (mouse) qtl MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20111116 MGI PMID:10436030 1301016 Szs1_m seizure susceptibility 1 (mouse) qtl MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20111116 MGI PMID:11472065 1301016 Szs1_m seizure susceptibility 1 (mouse) qtl MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20111116 MGI PMID:15112102 1301016 Szs1_m seizure susceptibility 1 (mouse) qtl MP:0002064 seizures IAGP N RGD:5509061 20111116 MGI PMID:9069121 1301016 Szs1_m seizure susceptibility 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1301016 Szs1_m seizure susceptibility 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1301019 Bmd6_m bone mineral density 6 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:11450694 1301019 Bmd6_m bone mineral density 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11450694 1301022 Morph4_m morphine antinociception 4 (mouse) qtl MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20111116 MGI PMID:11420618 1301022 Morph4_m morphine antinociception 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11420618 1301022 Morph4_m morphine antinociception 4 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11420618 1301023 Sluc24_m susceptibility to lung cancer 24 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1301023 Sluc24_m susceptibility to lung cancer 24 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301024 Tbrs2_m tuberculosis resistance 2 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:11197687 1301024 Tbrs2_m tuberculosis resistance 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11197687 1301025 Lbw7_m lupus NZB x NZW 7 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:7937857 1301025 Lbw7_m lupus NZB x NZW 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7937857 1301027 Hdlq12_m HDL QTL 12 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12588951 1301027 Hdlq12_m HDL QTL 12 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12588951 1301030 Bw4_m body weight QTL 4 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:9725853 1301030 Bw4_m body weight QTL 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9725853 1301031 Bdln3_m body length 3 (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20111116 MGI PMID:12856282 1301031 Bdln3_m body length 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12856282 1301032 Tauph_m tau phosphorylation (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12514215 1301032 Tauph_m tau phosphorylation (mouse) qtl MP:0004250 tau protein deposits IAGP N RGD:5509061 20140213 MGI PMID:12514215 1301033 Abbp2_m A/J and C57BL/6 blood pressure 2 (mouse) qtl MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20111116 MGI PMID:14612590 1301033 Abbp2_m A/J and C57BL/6 blood pressure 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14612590 1301034 Egrm2_m early growth rate (mouse) qtl MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20111116 MGI PMID:12242647 1301034 Egrm2_m early growth rate (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12242647 1301036 Axtofd4_m anxiety-open field defecation 4 (mouse) qtl MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:14990867 1301036 Axtofd4_m anxiety-open field defecation 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11454769|PMID:14990867 1301036 Axtofd4_m anxiety-open field defecation 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160422 MGI Created by mouse qtl pipeline PMID:14990867 1301036 Axtofd4_m anxiety-open field defecation 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160506 MGI Created by mouse qtl pipeline PMID:11454769 1301037 Cd4ts5_m CD4 T cell subset 5 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12595899 1301037 Cd4ts5_m CD4 T cell subset 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301037 Cd4ts5_m CD4 T cell subset 5 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301037 Cd4ts5_m CD4 T cell subset 5 (mouse) qtl MP:0008049 increased memory T cell number IAGP N RGD:5509061 20111116 MGI PMID:12595899 1301038 C10bw3_m castaneus 10 week body weight 3 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:11003694 1301038 C10bw3_m castaneus 10 week body weight 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11003694 1301039 Cbm4_m cerebellum weight 4 (mouse) qtl MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20111116 MGI PMID:11438585 1301039 Cbm4_m cerebellum weight 4 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11438585 1301041 Prnr2_m prion resistance 2 (mouse) qtl MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20111116 MGI PMID:14704188 1301041 Prnr2_m prion resistance 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14704188 1301042 Elmaz1_m elevated maze behavior 1 (mouse) qtl MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20111116 MGI PMID:11420611 1301042 Elmaz1_m elevated maze behavior 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11420611 1301045 Sluc10_m susceptibility to lung cancer 10 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9809979 1301045 Sluc10_m susceptibility to lung cancer 10 (mouse) qtl MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301045 Sluc10_m susceptibility to lung cancer 10 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301045 Sluc10_m susceptibility to lung cancer 10 (mouse) qtl MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301045 Sluc10_m susceptibility to lung cancer 10 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9809979 1301046 Par3_m pulmonary adenoma resistance 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11195459 1301046 Par3_m pulmonary adenoma resistance 3 (mouse) qtl MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20111116 MGI PMID:11195459 1301046 Par3_m pulmonary adenoma resistance 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11195459 1301047 Bglq9_m body growth late QTL 9 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:8846907 1301047 Bglq9_m body growth late QTL 9 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8846907 1301048 Actre2_m activity response to ethanol 2 (mouse) qtl MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20111116 MGI PMID:11529277 1301048 Actre2_m activity response to ethanol 2 (mouse) qtl MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20111116 MGI PMID:17143586 1301048 Actre2_m activity response to ethanol 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17143586|PMID:11529277 1301048 Actre2_m activity response to ethanol 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20151225 MGI Created by mouse qtl pipeline PMID:11529277 1301049 El4_m epilepsy 4 (mouse) qtl MP:0002064 seizures IAGP N RGD:5509061 20111116 MGI PMID:17010098 1301049 El4_m epilepsy 4 (mouse) qtl MP:0002064 seizures IAGP N RGD:5509061 20111116 MGI PMID:8747920 1301049 El4_m epilepsy 4 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8747920 1301049 El4_m epilepsy 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8747920 1301051 Eae9_m susceptibility to experimental allergic encephalomyelitis 9 (mouse) qtl MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:9712054 1301051 Eae9_m susceptibility to experimental allergic encephalomyelitis 9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7561115|PMID:9712054 1301051 Eae9_m susceptibility to experimental allergic encephalomyelitis 9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20160729 MGI Created by mouse qtl pipeline PMID:9712054 1301053 Idd6_m insulin dependent diabetes susceptibility 6 (mouse) qtl MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20111116 MGI PMID:12829632 1301053 Idd6_m insulin dependent diabetes susceptibility 6 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:11160299 1301053 Idd6_m insulin dependent diabetes susceptibility 6 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:11386752 1301053 Idd6_m insulin dependent diabetes susceptibility 6 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:7556956 1301053 Idd6_m insulin dependent diabetes susceptibility 6 (mouse) qtl MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:11484085 1301053 Idd6_m insulin dependent diabetes susceptibility 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11386752|PMID:8401590|PMID:11484085|PMID:11160299|PMID:7556956 1301053 Idd6_m insulin dependent diabetes susceptibility 6 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11386752|PMID:8401590|PMID:11484085|PMID:11160299|PMID:7556956 1301053 Idd6_m insulin dependent diabetes susceptibility 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11386752|PMID:8401590|PMID:11484085|PMID:11160299|PMID:7556956 1301053 Idd6_m insulin dependent diabetes susceptibility 6 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11386752|PMID:8401590|PMID:11484085|PMID:11160299|PMID:7556956 1301053 Idd6_m insulin dependent diabetes susceptibility 6 (mouse) qtl MP:0006043 decreased apoptosis IAGP N RGD:5509061 20111116 MGI PMID:12829632 1301053 Idd6_m insulin dependent diabetes susceptibility 6 (mouse) qtl MP:0008045 decreased NK cell number IAGP N RGD:5509061 20111116 MGI PMID:18641312 1301053 Idd6_m insulin dependent diabetes susceptibility 6 (mouse) qtl MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20111116 MGI PMID:18641312 1301053 Idd6_m insulin dependent diabetes susceptibility 6 (mouse) qtl MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20111116 MGI PMID:18641312 1301053 Idd6_m insulin dependent diabetes susceptibility 6 (mouse) qtl MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20111116 MGI PMID:12759418 1301054 Pcpila3_m PCP induced locomotor activity 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8914121 1301054 Pcpila3_m PCP induced locomotor activity 3 (mouse) qtl MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20111116 MGI PMID:8914121 1301056 Pas2_m pulmonary adenoma susceptibility 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12810665|PMID:7813906 1301056 Pas2_m pulmonary adenoma susceptibility 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20160212 MGI Created by mouse qtl pipeline PMID:7813906|PMID:12810665 1301057 Nidd4_m non-insulin-dependent diabetes mellitus 4 (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:10331427 1301057 Nidd4_m non-insulin-dependent diabetes mellitus 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10331427 1301058 Musz2_m muscle size 2 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:12185459 1301058 Musz2_m muscle size 2 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12185459 1301059 Hrtfm1_m heart failure modifier 1 (mouse) qtl MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20111116 MGI PMID:11956126 1301059 Hrtfm1_m heart failure modifier 1 (mouse) qtl MP:0002083 premature death IAGP N RGD:5509061 20111116 MGI PMID:11956126 1301059 Hrtfm1_m heart failure modifier 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11956126 1301059 Hrtfm1_m heart failure modifier 1 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11956126 1301061 Nidd5_m non-insulin-dependent diabetes mellitus 5 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:10331427 1301061 Nidd5_m non-insulin-dependent diabetes mellitus 5 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16688528 1301061 Nidd5_m non-insulin-dependent diabetes mellitus 5 (mouse) qtl MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:10331427 1301061 Nidd5_m non-insulin-dependent diabetes mellitus 5 (mouse) qtl MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20111116 MGI PMID:10331427 1301061 Nidd5_m non-insulin-dependent diabetes mellitus 5 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10331427 1301061 Nidd5_m non-insulin-dependent diabetes mellitus 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10331427 1301061 Nidd5_m non-insulin-dependent diabetes mellitus 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10331427 1301061 Nidd5_m non-insulin-dependent diabetes mellitus 5 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10331427 1301061 Nidd5_m non-insulin-dependent diabetes mellitus 5 (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:16688528 1301062 Pltpq4_m phospholipid transfer protein activity QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592843 1301062 Pltpq4_m phospholipid transfer protein activity QTL 4 (mouse) qtl MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20111116 MGI PMID:14592843 1301064 Bwq4_m body weight (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11515095 1301064 Bwq4_m body weight (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11515095 1301065 Morph3_m morphine antinociception 3 (mouse) qtl MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20111116 MGI PMID:11420618 1301065 Morph3_m morphine antinociception 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11420618 1301065 Morph3_m morphine antinociception 3 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11420618 1301066 Otx2m2_m orthodenticle homolog 2 (Drosophila) modifier 2 (mouse) qtl MP:0000087 absent mandible IAGP N RGD:5509061 20111116 MGI PMID:12183386 1301066 Otx2m2_m orthodenticle homolog 2 (Drosophila) modifier 2 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12183386 1301066 Otx2m2_m orthodenticle homolog 2 (Drosophila) modifier 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12183386 1301069 Bw10_m body weight QTL 10 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:9725853 1301069 Bw10_m body weight QTL 10 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9725853 1301070 Cypr1_m cytokine production 1 (mouse) qtl MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20111116 MGI PMID:9887350 1301070 Cypr1_m cytokine production 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9887350 1301072 Eae22_m experimental allergic encephalomyelitis 22 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10934166 1301072 Eae22_m experimental allergic encephalomyelitis 22 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10934166 1301072 Eae22_m experimental allergic encephalomyelitis 22 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10934166 1301072 Eae22_m experimental allergic encephalomyelitis 22 (mouse) qtl MP:0021002 brain lesion IAGP N RGD:5509061 20210805 MGI PMID:10934166 1301073 Orch5_m autoimmune orchitis resistance 5 (mouse) qtl MP:0001875 testis inflammation IAGP N RGD:5509061 20111116 MGI PMID:7777570 1301073 Orch5_m autoimmune orchitis resistance 5 (mouse) qtl MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:7777570 1301073 Orch5_m autoimmune orchitis resistance 5 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20141219 MGI Created by mouse qtl pipeline PMID:7777570 1301073 Orch5_m autoimmune orchitis resistance 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7777570 1301073 Orch5_m autoimmune orchitis resistance 5 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7777570 1301074 Axtofa3_m anxiety-open field activity 3 (mouse) qtl MP:0001399 hyperactivity IAGP N RGD:5509061 20111116 MGI PMID:14990867 1301074 Axtofa3_m anxiety-open field activity 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11454769|PMID:14990867 1301074 Axtofa3_m anxiety-open field activity 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160422 MGI Created by mouse qtl pipeline PMID:14990867 1301074 Axtofa3_m anxiety-open field activity 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160506 MGI Created by mouse qtl pipeline PMID:11454769 1301075 Obq10_m obesity QTL 10 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11210195 1301075 Obq10_m obesity QTL 10 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11210195 1301076 Idd10_m insulin dependent diabetes susceptibility 10 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:15850792 1301076 Idd10_m insulin dependent diabetes susceptibility 10 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:9257847 1301076 Idd10_m insulin dependent diabetes susceptibility 10 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:9530623 1301076 Idd10_m insulin dependent diabetes susceptibility 10 (mouse) qtl MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20111116 MGI PMID:12759418 1301076 Idd10_m insulin dependent diabetes susceptibility 10 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8401590|PMID:9257847|PMID:15850792|PMID:7556956 1301076 Idd10_m insulin dependent diabetes susceptibility 10 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20180330 MGI Created by mouse qtl pipeline PMID:9257847|PMID:15850792|PMID:8401590|PMID:7556956 1301076 Idd10_m insulin dependent diabetes susceptibility 10 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8401590|PMID:9257847|PMID:15850792|PMID:7556956 1301076 Idd10_m insulin dependent diabetes susceptibility 10 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20180330 MGI Created by mouse qtl pipeline PMID:9257847|PMID:15850792|PMID:8401590|PMID:7556956 1301076 Idd10_m insulin dependent diabetes susceptibility 10 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:8401590|PMID:9257847|PMID:15850792|PMID:7556956 1301076 Idd10_m insulin dependent diabetes susceptibility 10 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20180330 MGI Created by mouse qtl pipeline PMID:9257847|PMID:15850792|PMID:8401590|PMID:7556956 1301076 Idd10_m insulin dependent diabetes susceptibility 10 (mouse) qtl MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20111116 MGI PMID:12759418 1301077 Pcpila1_m PCP induced locomotor activity 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8914121 1301077 Pcpila1_m PCP induced locomotor activity 1 (mouse) qtl MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20111116 MGI PMID:8914121 1301078 Alcp2_m alcohol preference locus 2 (mouse) qtl MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20120301 MGI PMID:8640219 1301078 Alcp2_m alcohol preference locus 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8640219 1301080 Sluc9_m susceptibility to lung cancer 9 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9809979 1301080 Sluc9_m susceptibility to lung cancer 9 (mouse) qtl MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301080 Sluc9_m susceptibility to lung cancer 9 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301080 Sluc9_m susceptibility to lung cancer 9 (mouse) qtl MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301080 Sluc9_m susceptibility to lung cancer 9 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9809979 1301081 Cfsw3_m cystic fibrosis survival to weaning 3 (mouse) qtl MP:0002082 postnatal lethality IAGP N RGD:5509061 20111116 MGI PMID:12441405 1301081 Cfsw3_m cystic fibrosis survival to weaning 3 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12441405 1301082 Bbaa16_m B.burgdorferi-associated arthritis 16 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11704805 1301082 Bbaa16_m B.burgdorferi-associated arthritis 16 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11704805 1301083 Bhr5_m bronchial hyperresponsiveness 5 (mouse) qtl MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20150402 MGI PMID:8624254 1301083 Bhr5_m bronchial hyperresponsiveness 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10600881|PMID:15657107 1301083 Bhr5_m bronchial hyperresponsiveness 5 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10600881|PMID:15657107 1301083 Bhr5_m bronchial hyperresponsiveness 5 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:8624254 1301084 Bpq5_m blood pressure QTL 5 (mouse) qtl MP:0000231 hypertension IAGP N RGD:5509061 20111116 MGI PMID:11161799 1301084 Bpq5_m blood pressure QTL 5 (mouse) qtl MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20111116 MGI PMID:11161799 1301084 Bpq5_m blood pressure QTL 5 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11161799 1301085 Lrnx10_m learning-contextual 10 (mouse) qtl MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20111116 MGI PMID:9354800 1301085 Lrnx10_m learning-contextual 10 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9354800 1301086 Lprm5_m lymphoproliferation modifier 5 (mouse) qtl MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20111116 MGI PMID:9403730 1301086 Lprm5_m lymphoproliferation modifier 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9403730 1301087 Bbaa15_m B.burgdorferi-associated arthritis 15 (mouse) qtl MP:0002493 increased IgG level IAGP N RGD:5509061 20111116 MGI PMID:11704805 1301087 Bbaa15_m B.burgdorferi-associated arthritis 15 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11704805 1301087 Bbaa15_m B.burgdorferi-associated arthritis 15 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:11704805 1301090 Eae23_m experimental allergic encephalomyelitis 23 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10934166 1301090 Eae23_m experimental allergic encephalomyelitis 23 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10934166 1301090 Eae23_m experimental allergic encephalomyelitis 23 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10934166 1301090 Eae23_m experimental allergic encephalomyelitis 23 (mouse) qtl MP:0021002 brain lesion IAGP N RGD:5509061 20210805 MGI PMID:10934166 1301091 Bbaa21_m B.burgdorferi-associated arthritis 21 (mouse) qtl MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:11704805 1301091 Bbaa21_m B.burgdorferi-associated arthritis 21 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11704805 1301093 Igfbp3q2_m insulin-like growth factor binding protein 3 QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11292658 1301093 Igfbp3q2_m insulin-like growth factor binding protein 3 QTL 2 (mouse) qtl MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20111116 MGI PMID:11292658 1301095 El6_m epilepsy 6 (mouse) qtl MP:0002064 seizures IAGP N RGD:5509061 20111116 MGI PMID:8747920 1301095 El6_m epilepsy 6 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8747920 1301095 El6_m epilepsy 6 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8747920 1301096 Obq1_m obesity QTL 1 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:8786140 1301096 Obq1_m obesity QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8786140 1301097 Bplpf1_m bleomycin pulmonary fibrosis 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:9393751 1301097 Bplpf1_m bleomycin pulmonary fibrosis 1 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9393751 1301097 Bplpf1_m bleomycin pulmonary fibrosis 1 (mouse) qtl MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20111116 MGI PMID:9393751 1301098 Cd8mts3_m CD8 memory T cell subset 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301098 Cd8mts3_m CD8 memory T cell subset 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301098 Cd8mts3_m CD8 memory T cell subset 3 (mouse) qtl MP:0008049 increased memory T cell number IAGP N RGD:5509061 20111116 MGI PMID:12595899 1301099 Cbm2_m cerebellum weight 2 (mouse) qtl MP:0000774 decreased brain size IAGP N RGD:5509061 20111116 MGI PMID:11438585 1301099 Cbm2_m cerebellum weight 2 (mouse) qtl MP:0002175 decreased brain weight IAGP N RGD:5509061 20111116 MGI PMID:11438585 1301099 Cbm2_m cerebellum weight 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11438585 1301101 Hpnr4_m Heligmosomoides polygyrus nematode resistance 4 (mouse) qtl MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20111116 MGI PMID:14507332 1301103 Pgia11_m proteoglycan induced arthritis 11 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:10615997 1301103 Pgia11_m proteoglycan induced arthritis 11 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10615997|PMID:15084914 1301103 Pgia11_m proteoglycan induced arthritis 11 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:10615997 1301105 Cfld4_m cystic fibrosis lung disease 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:12461645 1301105 Cfld4_m cystic fibrosis lung disease 4 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12461645 1301105 Cfld4_m cystic fibrosis lung disease 4 (mouse) qtl MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20111116 MGI PMID:12461645 1301106 Skts7_m skin tumor susceptibility 7 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1301106 Skts7_m skin tumor susceptibility 7 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:10611333 1301106 Skts7_m skin tumor susceptibility 7 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1301107 Scc4_m colon tumor susceptibility 4 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8944029 1301107 Scc4_m colon tumor susceptibility 4 (mouse) qtl MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8944029 1301107 Scc4_m colon tumor susceptibility 4 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:8944029 1301108 Scon2_m sucrose consumption 2 (mouse) qtl MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20111116 MGI PMID:9250857 1301108 Scon2_m sucrose consumption 2 (mouse) qtl MP:0005394 taste/olfaction phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9250857|PMID:10776660 1301108 Scon2_m sucrose consumption 2 (mouse) qtl MP:0005394 taste/olfaction phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:9250857 1301109 Dntcs2_m dental caries susceptibility 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:14767162 1301109 Dntcs2_m dental caries susceptibility 2 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14767162 1301109 Dntcs2_m dental caries susceptibility 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20170929 MGI Created by mouse qtl pipeline PMID:14767162 1301109 Dntcs2_m dental caries susceptibility 2 (mouse) qtl MP:0030101 carious teeth IAGP N RGD:5509061 20170928 MGI PMID:14767162 1301111 Mwq2_m molecular weight of quadriceps QTL 2 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:11116089 1301111 Mwq2_m molecular weight of quadriceps QTL 2 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089 1301112 Szs9_m seizure susceptibility 9 (mouse) qtl MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20111116 MGI PMID:11472065 1301112 Szs9_m seizure susceptibility 9 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1301112 Szs9_m seizure susceptibility 9 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1301114 Ssial2_m susceptibility to sialadenitis 2 (mouse) qtl MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20111116 MGI PMID:11937580 1301114 Ssial2_m susceptibility to sialadenitis 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11937580 1301114 Ssial2_m susceptibility to sialadenitis 2 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11937580 1301114 Ssial2_m susceptibility to sialadenitis 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11937580 1301115 Lrdm1_m lymphoproliferation (Fas) renal disease modifier 1 (mouse) qtl MP:0001859 kidney inflammation IAGP N RGD:5509061 20111116 MGI PMID:1460423 1301115 Lrdm1_m lymphoproliferation (Fas) renal disease modifier 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9922399|PMID:1460423 1301115 Lrdm1_m lymphoproliferation (Fas) renal disease modifier 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20150724 MGI Created by mouse qtl pipeline PMID:1460423 1301115 Lrdm1_m lymphoproliferation (Fas) renal disease modifier 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9922399|PMID:1460423 1301115 Lrdm1_m lymphoproliferation (Fas) renal disease modifier 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150724 MGI Created by mouse qtl pipeline PMID:1460423 1301116 Hdlq5_m HDL QTL 5 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12805272 1301116 Hdlq5_m HDL QTL 5 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12805272 1301116 Hdlq5_m HDL QTL 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14872007|PMID:14701919|PMID:12805272 1301116 Hdlq5_m HDL QTL 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:12805272 1301117 Fecq1_m fecundity QTL 1 (mouse) qtl MP:0001934 increased litter size IAGP N RGD:5509061 20111116 MGI PMID:9457667 1301117 Fecq1_m fecundity QTL 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9457667 1301118 Bbaa23_m B.burgdorferi-associated arthritis 23 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11704805 1301118 Bbaa23_m B.burgdorferi-associated arthritis 23 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11431140 1301121 Obq13_m obesity QTL 13 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11210195 1301121 Obq13_m obesity QTL 13 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11210195 1301122 Cd8mts1_m CD8 T memory cell subset 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301122 Cd8mts1_m CD8 T memory cell subset 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301122 Cd8mts1_m CD8 T memory cell subset 1 (mouse) qtl MP:0008049 increased memory T cell number IAGP N RGD:5509061 20111116 MGI PMID:12595899 1301123 Cd8mts2_m CD8 memory T cell subset 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301123 Cd8mts2_m CD8 memory T cell subset 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301123 Cd8mts2_m CD8 memory T cell subset 2 (mouse) qtl MP:0008049 increased memory T cell number IAGP N RGD:5509061 20111116 MGI PMID:12595899 1301125 Sluc27_m susceptibility to lung cancer 27 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1301125 Sluc27_m susceptibility to lung cancer 27 (mouse) qtl MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301126 Bwem1_m body weight day 30 males 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:10086232 1301126 Bwem1_m body weight day 30 males 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10086232 1301127 Hpnr2_m Heligmosomoides polygyrus nematode resistance 2 (mouse) qtl MP:0002492 decreased IgE level IAGP N RGD:5509061 20111116 MGI PMID:14507332 1301127 Hpnr2_m Heligmosomoides polygyrus nematode resistance 2 (mouse) qtl MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20111116 MGI PMID:14507332 1301127 Hpnr2_m Heligmosomoides polygyrus nematode resistance 2 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:12647241 1301127 Hpnr2_m Heligmosomoides polygyrus nematode resistance 2 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:16783640 1301128 Sluc20_m susceptibility to lung cancer 20 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1301128 Sluc20_m susceptibility to lung cancer 20 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301128 Sluc20_m susceptibility to lung cancer 20 (mouse) qtl MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301130 Sle1a_m systematic lupus erythematosus susceptibility 1a (mouse) qtl MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20111116 MGI PMID:11172029 1301130 Sle1a_m systematic lupus erythematosus susceptibility 1a (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11172029 1301132 Mors1_m modifier of obesity related sterility 1 (mouse) qtl MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20111116 MGI PMID:9927300 1301132 Mors1_m modifier of obesity related sterility 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9927300 1301133 Mob8_m multigenic obesity 8 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:9616220 1301134 Bmd1_m bone mineral density 1 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:10556421 1301134 Bmd1_m bone mineral density 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10556421 1301135 Pas8_m pulmonary adenoma susceptibility 8 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9790761 1301135 Pas8_m pulmonary adenoma susceptibility 8 (mouse) qtl MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20111116 MGI PMID:9790761 1301135 Pas8_m pulmonary adenoma susceptibility 8 (mouse) qtl MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20111116 MGI PMID:9790761 1301135 Pas8_m pulmonary adenoma susceptibility 8 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9790761 1301135 Pas8_m pulmonary adenoma susceptibility 8 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9790761 1301136 Pgia8_m proteoglycan induced arthritis 8 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10615997 1301136 Pgia8_m proteoglycan induced arthritis 8 (mouse) qtl MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:18606685 1301136 Pgia8_m proteoglycan induced arthritis 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18606685|PMID:10615997|PMID:15084914 1301136 Pgia8_m proteoglycan induced arthritis 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150925 MGI Created by mouse qtl pipeline PMID:18606685|PMID:10615997 1301136 Pgia8_m proteoglycan induced arthritis 8 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18606685|PMID:10615997|PMID:15084914 1301136 Pgia8_m proteoglycan induced arthritis 8 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20150925 MGI Created by mouse qtl pipeline PMID:18606685|PMID:10615997 1301136 Pgia8_m proteoglycan induced arthritis 8 (mouse) qtl MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20111116 MGI PMID:18606685 1301136 Pgia8_m proteoglycan induced arthritis 8 (mouse) qtl MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20111116 MGI PMID:18606685 1301137 Cocia8_m cocaine induced activation 8 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12777963 1301137 Cocia8_m cocaine induced activation 8 (mouse) qtl MP:0008911 induced hyperactivity IAGP N RGD:5509061 20220421 MGI PMID:12777963 1301137 Cocia8_m cocaine induced activation 8 (mouse) qtl MP:0020871 abnormal locomotor response to cocaine IAGP N RGD:5509061 20220421 MGI PMID:12777963 1301138 Pcd4ts3_m p-glycoprotein positive CD4 T cell subset 3 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12595899 1301138 Pcd4ts3_m p-glycoprotein positive CD4 T cell subset 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301138 Pcd4ts3_m p-glycoprotein positive CD4 T cell subset 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301139 Lmr10_m leishmaniasis resistance 10 (mouse) qtl MP:0002492 decreased IgE level IAGP N RGD:5509061 20111116 MGI PMID:12058253 1301139 Lmr10_m leishmaniasis resistance 10 (mouse) qtl MP:0002497 increased IgE level IAGP N RGD:5509061 20111116 MGI PMID:12058253 1301139 Lmr10_m leishmaniasis resistance 10 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1301139 Lmr10_m leishmaniasis resistance 10 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:12058253 1301140 Bbaa12_m B.burgdorferi-associated arthritis 12 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11704805 1301140 Bbaa12_m B.burgdorferi-associated arthritis 12 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11704805 1301142 Heal2_m wound healing/regeneration 2 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:9751744 1301142 Heal2_m wound healing/regeneration 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12682777|PMID:9751744 1301142 Heal2_m wound healing/regeneration 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:9751744 1301143 Skull17_m skull morphology 17 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301143 Skull17_m skull morphology 17 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301143 Skull17_m skull morphology 17 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301145 Mob2_m multigenic obesity 2 (mouse) qtl MP:0009290 increased femoral fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:7706460 1301146 Obq11_m obesity QTL 11 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11210195 1301146 Obq11_m obesity QTL 11 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11210195 1301147 Diet1_m variability in response to cholestrol enriched atherogenic diet (mouse) qtl MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:10744778 1301147 Diet1_m variability in response to cholestrol enriched atherogenic diet (mouse) qtl MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1301147 Diet1_m variability in response to cholestrol enriched atherogenic diet (mouse) qtl MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1301147 Diet1_m variability in response to cholestrol enriched atherogenic diet (mouse) qtl MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1301147 Diet1_m variability in response to cholestrol enriched atherogenic diet (mouse) qtl MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1301147 Diet1_m variability in response to cholestrol enriched atherogenic diet (mouse) qtl MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1301147 Diet1_m variability in response to cholestrol enriched atherogenic diet (mouse) qtl MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1301147 Diet1_m variability in response to cholestrol enriched atherogenic diet (mouse) qtl MP:0002139 abnormal hepatobiliary system physiology IAGP N RGD:5509061 20111116 MGI PMID:11682476 1301147 Diet1_m variability in response to cholestrol enriched atherogenic diet (mouse) qtl MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1301147 Diet1_m variability in response to cholestrol enriched atherogenic diet (mouse) qtl MP:0005085 abnormal gallbladder physiology IAGP N RGD:5509061 20111116 MGI PMID:11682476 1301147 Diet1_m variability in response to cholestrol enriched atherogenic diet (mouse) qtl MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:10744778 1301147 Diet1_m variability in response to cholestrol enriched atherogenic diet (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10744778|PMID:11682476 1301147 Diet1_m variability in response to cholestrol enriched atherogenic diet (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10744778|PMID:11682476 1301150 Cara3_m carcass ash in high growth mice 3 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:11309659 1301150 Cara3_m carcass ash in high growth mice 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301151 Hdlq14_m HDL QTL 14 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14592847 1301151 Hdlq14_m HDL QTL 14 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14592847 1301151 Hdlq14_m HDL QTL 14 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592847 1301152 Athsq2_m atherosclerosis susceptibility QTL 2 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:11438740 1301152 Athsq2_m atherosclerosis susceptibility QTL 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11438740 1301153 Estq3_m estradiol regulated response QTL 3 (mouse) qtl MP:0004904 increased uterus weight IAGP N RGD:5509061 20111116 MGI PMID:9927277 1301153 Estq3_m estradiol regulated response QTL 3 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9927277 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0001869 pancreas inflammation IAGP N RGD:5509061 20111116 MGI PMID:11016460 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0001873 stomach inflammation IAGP N RGD:5509061 20111116 MGI PMID:16172259 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:10955330 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:11016460 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:15905556 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:8661724 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20111116 MGI PMID:16172259 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10955330|PMID:8661724|PMID:15905556|PMID:11016460|PMID:8401590|PMID:8384947 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20131011 MGI Created by mouse qtl pipeline PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20220121 MGI Created by mouse qtl pipeline PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590|PMID:26512207 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10955330|PMID:8661724|PMID:15905556|PMID:11016460|PMID:8401590|PMID:8384947 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20131011 MGI Created by mouse qtl pipeline PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20220121 MGI Created by mouse qtl pipeline PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590|PMID:26512207 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10955330|PMID:8661724|PMID:15905556|PMID:11016460|PMID:8401590|PMID:8384947 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20131011 MGI Created by mouse qtl pipeline PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20220121 MGI Created by mouse qtl pipeline PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590|PMID:26512207 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10955330|PMID:8661724|PMID:15905556|PMID:11016460|PMID:8401590|PMID:8384947 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20131011 MGI Created by mouse qtl pipeline PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20220121 MGI Created by mouse qtl pipeline PMID:10955330|PMID:8661724|PMID:8384947|PMID:15905556|PMID:11016460|PMID:8401590|PMID:26512207 1301154 Idd5_m insulin dependent diabetes susceptibility 5 (mouse) qtl MP:0005580 periinsulitis IAGP N RGD:5509061 20111116 MGI PMID:8661724 1301155 Bpq7_m blood pressure QTL 7 (mouse) qtl MP:0000231 hypertension IAGP N RGD:5509061 20111116 MGI PMID:12118100 1301155 Bpq7_m blood pressure QTL 7 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118100 1301156 Lbm1_m lean body mass 1 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:12185457 1301156 Lbm1_m lean body mass 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12185457 1301157 Wt10q1_m body weight (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:10353911 1301157 Wt10q1_m body weight (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1301158 Eae4_m susceptibility to experimental allergic encephalomyelitis 4 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:7561115 1301158 Eae4_m susceptibility to experimental allergic encephalomyelitis 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7561115|PMID:10072563 1301158 Eae4_m susceptibility to experimental allergic encephalomyelitis 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150717 MGI Created by mouse qtl pipeline PMID:7561115 1301159 Fob4_m F-line obesity QTL 4 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:10602985 1301159 Fob4_m F-line obesity QTL 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10602985 1301160 Eae14_m susceptibility to experimental allergic encephalomyelitis 14 (mouse) qtl MP:0000921 demyelination IAGP N RGD:5509061 20111116 MGI PMID:10706738 1301160 Eae14_m susceptibility to experimental allergic encephalomyelitis 14 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10706738 1301160 Eae14_m susceptibility to experimental allergic encephalomyelitis 14 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:10706738 1301160 Eae14_m susceptibility to experimental allergic encephalomyelitis 14 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10706738 1301162 Skull1_m skull morphology 1 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301162 Skull1_m skull morphology 1 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301162 Skull1_m skull morphology 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301163 Eae16_m susceptibility to experimental allergic encephalomyelitis 16 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10934166 1301163 Eae16_m susceptibility to experimental allergic encephalomyelitis 16 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10934166 1301163 Eae16_m susceptibility to experimental allergic encephalomyelitis 16 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10934166 1301163 Eae16_m susceptibility to experimental allergic encephalomyelitis 16 (mouse) qtl MP:0021002 brain lesion IAGP N RGD:5509061 20210805 MGI PMID:10934166 1301165 Lith7_m lithogenic gene 7 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:12949731 1301165 Lith7_m lithogenic gene 7 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12949731 1301166 Thypr2_m thymocyte proliferative response 2 (mouse) qtl MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:12044964 1301166 Thypr2_m thymocyte proliferative response 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12044964 1301166 Thypr2_m thymocyte proliferative response 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12044964 1301166 Thypr2_m thymocyte proliferative response 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12044964 1301167 Bgeq2_m body growth early QTL 2 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:8846907 1301167 Bgeq2_m body growth early QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10689807 1301170 Lith13_m lithogenic gene 13 (mouse) qtl MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20111116 MGI PMID:12837957 1301170 Lith13_m lithogenic gene 13 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12837957 1301172 Fembrs6_m femur breaking strength 6 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:11991724 1301172 Fembrs6_m femur breaking strength 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11991724 1301175 Ap7q_m alcohol preference 7 QTL (mouse) qtl MP:0001425 abnormal alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:12176933 1301175 Ap7q_m alcohol preference 7 QTL (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12176933 1301177 Vent3_m ventricular size 3 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12746874 1301177 Vent3_m ventricular size 3 (mouse) qtl MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20140220 MGI PMID:12746874 1301178 Lith10_m lithogenic gene 10 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:12810825 1301178 Lith10_m lithogenic gene 10 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12810825 1301179 Fembm4_m femoral bone morphometry 4 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11518254 1301179 Fembm4_m femoral bone morphometry 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11518254 1301179 Fembm4_m femoral bone morphometry 4 (mouse) qtl MP:0030823 increased femur size IAGP N RGD:5509061 20181018 MGI PMID:11518254 1301181 Lbm6_m lean body mass 6 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:12185457 1301181 Lbm6_m lean body mass 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12185457 1301183 Cadfar_m cadmium-induced forelimb autopod reduction defect (mouse) qtl MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20111116 MGI PMID:10673332 1301183 Cadfar_m cadmium-induced forelimb autopod reduction defect (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10673332 1301184 Bdln4_m body length 4 (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20111116 MGI PMID:12856282 1301184 Bdln4_m body length 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12856282 1301185 Hdlq4_m HDL QTL 4 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12006675 1301185 Hdlq4_m HDL QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12006675 1301186 Hlq2_m heat loss QTL 2 (mouse) qtl MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20111116 MGI PMID:10353911 1301186 Hlq2_m heat loss QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1301187 Adip9_m adiposity 9 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:12856282 1301187 Adip9_m adiposity 9 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12856282 1301188 Heal6_m wound healing/regeneration 6 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:9751744 1301188 Heal6_m wound healing/regeneration 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12682777|PMID:9751744 1301188 Heal6_m wound healing/regeneration 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:9751744 1301189 Lmr8_m leishmaniasis resistance 8 (mouse) qtl MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20111116 MGI PMID:16511555 1301189 Lmr8_m leishmaniasis resistance 8 (mouse) qtl MP:0002492 decreased IgE level IAGP N RGD:5509061 20111116 MGI PMID:12058253 1301189 Lmr8_m leishmaniasis resistance 8 (mouse) qtl MP:0002497 increased IgE level IAGP N RGD:5509061 20111116 MGI PMID:12058253 1301189 Lmr8_m leishmaniasis resistance 8 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12058253 1301189 Lmr8_m leishmaniasis resistance 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1301189 Lmr8_m leishmaniasis resistance 8 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1301190 Cd4ts2_m CD4 T cell subset 2 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12595899 1301190 Cd4ts2_m CD4 T cell subset 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301190 Cd4ts2_m CD4 T cell subset 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301191 Stia1_m serum transfer induced arthritis 1 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11489951 1301191 Stia1_m serum transfer induced arthritis 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11489951 1301192 Skts6_m skin tumor susceptibility 6 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1301192 Skts6_m skin tumor susceptibility 6 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:10611333 1301192 Skts6_m skin tumor susceptibility 6 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1301193 Lxw3_m lupus BXSB x NZW 3 (mouse) qtl MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20111116 MGI PMID:14662843 1301193 Lxw3_m lupus BXSB x NZW 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14662843 1301196 Mnif1_m macronutrient intake (mouse) qtl MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20111116 MGI PMID:12388789 1301196 Mnif1_m macronutrient intake (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12388789 1301197 Tlyr1_m thymic lymphoma resistance 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12242666 1301197 Tlyr1_m thymic lymphoma resistance 1 (mouse) qtl MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:12242666 1301198 Hdlq3_m HDL QTL 3 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12006675 1301198 Hdlq3_m HDL QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12006675 1301200 Mob1_m multigenic obesity 1 (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20111116 MGI PMID:14981222 1301200 Mob1_m multigenic obesity 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:14981222 1301200 Mob1_m multigenic obesity 1 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:7706460 1301200 Mob1_m multigenic obesity 1 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14981222 1301200 Mob1_m multigenic obesity 1 (mouse) qtl MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:7706460 1301200 Mob1_m multigenic obesity 1 (mouse) qtl MP:0005449 abnormal food intake IAGP N RGD:5509061 20111116 MGI PMID:14981222 1301200 Mob1_m multigenic obesity 1 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:14981222 1301200 Mob1_m multigenic obesity 1 (mouse) qtl MP:0005534 decreased body temperature IAGP N RGD:5509061 20111116 MGI PMID:14981222 1301200 Mob1_m multigenic obesity 1 (mouse) qtl MP:0010024 increased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:14981222 1301200 Mob1_m multigenic obesity 1 (mouse) qtl MP:0010024 increased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:7706460 1301200 Mob1_m multigenic obesity 1 (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:7706460 1301200 Mob1_m multigenic obesity 1 (mouse) qtl MP:0011582 decreased triglyceride lipase activity IAGP N RGD:5509061 20120209 MGI PMID:14981222 1301200 Mob1_m multigenic obesity 1 (mouse) qtl MP:0011582 decreased triglyceride lipase activity IAGP N RGD:5509061 20120209 MGI PMID:7706460 1301201 Chab1_m cholesterol absorption 1 (mouse) qtl MP:0002646 increased intestinal cholesterol absorption IAGP N RGD:5509061 20111116 MGI PMID:11714849 1301201 Chab1_m cholesterol absorption 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11714849 1301201 Chab1_m cholesterol absorption 1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11714849 1301202 Yaa4_m Y-linked autoimmune acceleration 4 (mouse) qtl MP:0001859 kidney inflammation IAGP N RGD:5509061 20111116 MGI PMID:9743333 1301202 Yaa4_m Y-linked autoimmune acceleration 4 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9743333 1301202 Yaa4_m Y-linked autoimmune acceleration 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9743333 1301204 Mob4_m Multigenic obesity 4 (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:7706460 1301205 Cms2_m resistance to Coccidioides immitis 2 (mouse) qtl MP:0002409 decreased susceptibility to infection IAGP N RGD:5509061 20111116 MGI PMID:10338499 1301205 Cms2_m resistance to Coccidioides immitis 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10338499 1301206 Idd12_m insulin dependent diabetes susceptibility 12 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:8016086 1301206 Idd12_m insulin dependent diabetes susceptibility 12 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8016086 1301207 Circp1_m circadian photosensitivity 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12465884 1301207 Circp1_m circadian photosensitivity 1 (mouse) qtl MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:12465884 1301210 Krcn_m keratoconus (mouse) qtl MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20111116 MGI PMID:11773012 1301211 Bbaa11_m B.burgdorferi-associated arthritis 11 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11704805 1301211 Bbaa11_m B.burgdorferi-associated arthritis 11 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11704805 1301212 Bw19_m body weight QTL 19 (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20111116 MGI PMID:11535651 1301212 Bw19_m body weight QTL 19 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:11535651 1301212 Bw19_m body weight QTL 19 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:11535651 1301212 Bw19_m body weight QTL 19 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9449189 1301212 Bw19_m body weight QTL 19 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9449189 1301212 Bw19_m body weight QTL 19 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9449189 1301212 Bw19_m body weight QTL 19 (mouse) qtl MP:0011939 increased food intake IAGP N RGD:5509061 20130328 MGI PMID:11535651 1301215 Thcr_m T helper cell response (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14568935 1301215 Thcr_m T helper cell response (mouse) qtl MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20111116 MGI PMID:14568935 1301215 Thcr_m T helper cell response (mouse) qtl MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20111116 MGI PMID:14568935 1301215 Thcr_m T helper cell response (mouse) qtl MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20111116 MGI PMID:14568935 1301215 Thcr_m T helper cell response (mouse) qtl MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20111116 MGI PMID:14568935 1301216 Cbm1_m cerebellum weight 1 (mouse) qtl MP:0000774 decreased brain size IAGP N RGD:5509061 20111116 MGI PMID:11438585 1301216 Cbm1_m cerebellum weight 1 (mouse) qtl MP:0002175 decreased brain weight IAGP N RGD:5509061 20111116 MGI PMID:11438585 1301216 Cbm1_m cerebellum weight 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11438585 1301220 Chol4_m cholesterol 4 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:10101257 1301220 Chol4_m cholesterol 4 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16679719 1301221 Hrtfm2_m heart failure modifier 2 (mouse) qtl MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20111116 MGI PMID:11956126 1301221 Hrtfm2_m heart failure modifier 2 (mouse) qtl MP:0002082 postnatal lethality IAGP N RGD:5509061 20111116 MGI PMID:16075368 1301221 Hrtfm2_m heart failure modifier 2 (mouse) qtl MP:0002083 premature death IAGP N RGD:5509061 20111116 MGI PMID:11956126 1301221 Hrtfm2_m heart failure modifier 2 (mouse) qtl MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20111116 MGI PMID:16075368 1301221 Hrtfm2_m heart failure modifier 2 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16075368|PMID:11956126 1301221 Hrtfm2_m heart failure modifier 2 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:11956126 1301221 Hrtfm2_m heart failure modifier 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16075368|PMID:11956126 1301221 Hrtfm2_m heart failure modifier 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:11956126 1301221 Hrtfm2_m heart failure modifier 2 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16075368|PMID:11956126 1301221 Hrtfm2_m heart failure modifier 2 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:11956126 1301222 Scc7_m colon tumor susceptibility 7 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10485458 1301222 Scc7_m colon tumor susceptibility 7 (mouse) qtl MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20111116 MGI PMID:10485458 1301222 Scc7_m colon tumor susceptibility 7 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:10485458 1301223 Hdlq7_m HDL QTL 7 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12805272 1301223 Hdlq7_m HDL QTL 7 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12805272 1301223 Hdlq7_m HDL QTL 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12805272 1301224 Carfhg1_m carcass fat in high growth mice 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301224 Carfhg1_m carcass fat in high growth mice 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:11309659 1301224 Carfhg1_m carcass fat in high growth mice 1 (mouse) qtl MP:0010024 increased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:11309659 1301225 Sle7_m systematic lupus erythematosus susceptibility 7 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:10693874 1301225 Sle7_m systematic lupus erythematosus susceptibility 7 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10693874 1301225 Sle7_m systematic lupus erythematosus susceptibility 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10693874 1301226 Bbaa2_m B.burgdorferi-associated arthritis 2 (mouse) qtl MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20111116 MGI PMID:9916719 1301226 Bbaa2_m B.burgdorferi-associated arthritis 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9916719 1301227 Skull19_m skull morphology 19 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301227 Skull19_m skull morphology 19 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301227 Skull19_m skull morphology 19 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301228 Iba4_m induction of brown adipocytes 4 (mouse) qtl MP:0003012 obsolete no phenotypic analysis IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10931824 1301229 Bpq1_m blood pressure QTL 1 (mouse) qtl MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20111116 MGI PMID:11161799 1301229 Bpq1_m blood pressure QTL 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11161799 1301230 Idd5b_m insulin dependent diabetes susceptibility 5b (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:11016460 1301230 Idd5b_m insulin dependent diabetes susceptibility 5b (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:15210771 1301230 Idd5b_m insulin dependent diabetes susceptibility 5b (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:18056379 1301230 Idd5b_m insulin dependent diabetes susceptibility 5b (mouse) qtl MP:0004031 insulitis IAGP N RGD:5509061 20111116 MGI PMID:18056379 1301231 Chab6_m cholesterol absorption 6 (mouse) qtl MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20111116 MGI PMID:11714849 1301231 Chab6_m cholesterol absorption 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11714849 1301231 Chab6_m cholesterol absorption 6 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11714849 1301232 Hcs7_m hepatocarcinogenesis susceptibility 7 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15238534 1301232 Hcs7_m hepatocarcinogenesis susceptibility 7 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20151113 MGI Created by mouse qtl pipeline 1301232 Hcs7_m hepatocarcinogenesis susceptibility 7 (mouse) qtl MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20111116 MGI PMID:15238534 1301232 Hcs7_m hepatocarcinogenesis susceptibility 7 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline 1301232 Hcs7_m hepatocarcinogenesis susceptibility 7 (mouse) qtl MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20111116 MGI PMID:15238534 1301232 Hcs7_m hepatocarcinogenesis susceptibility 7 (mouse) qtl MP:0010266 decreased liver tumor incidence IEA N RGD:5509061 20111116 MGI 1301233 Sbw2_m splenomegaly-NZB x NZW 2 (mouse) qtl MP:0000691 enlarged spleen IAGP N RGD:5509061 20111116 MGI PMID:7937857 1301233 Sbw2_m splenomegaly-NZB x NZW 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:7937857 1301233 Sbw2_m splenomegaly-NZB x NZW 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7937857 1301233 Sbw2_m splenomegaly-NZB x NZW 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7937857 1301234 Hscfr_m hematopoietic stem cell frequency regulator (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:11777956 1301234 Hscfr_m hematopoietic stem cell frequency regulator (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11777956 1301235 Alcw4_m alcohol withdrawal 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8974318 1301235 Alcw4_m alcohol withdrawal 4 (mouse) qtl MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20111116 MGI PMID:8974318 1301240 Sluc15_m susceptibility to lung cancer 15 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1301240 Sluc15_m susceptibility to lung cancer 15 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301241 Renf1_m renal failure 1 (mouse) qtl MP:0003606 kidney failure IAGP N RGD:5509061 20111116 MGI PMID:11839593 1301241 Renf1_m renal failure 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11839593 1301242 Lbm5_m lean body mass 5 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:12185457 1301242 Lbm5_m lean body mass 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12185457 1301243 Bmd2_m bone mineral density 2 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:10556421 1301243 Bmd2_m bone mineral density 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10556421 1301244 Ichs_m immediate cutaneous hypersensitivity QTL (mouse) qtl MP:0002531 abnormal type I hypersensitivity reaction IAGP N RGD:5509061 20111116 MGI PMID:10941834 1301244 Ichs_m immediate cutaneous hypersensitivity QTL (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10941834 1301247 Chol3_m cholesterol 3 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:10101257 1301248 Alaa1_m alopecia areata (mouse) qtl MP:0000414 alopecia IAGP N RGD:5509061 20111116 MGI PMID:12713579 1301248 Alaa1_m alopecia areata (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12713579 1301249 Sbw1_m splenomegaly-NZB x NZW 1 (mouse) qtl MP:0000691 enlarged spleen IAGP N RGD:5509061 20111116 MGI PMID:7937857 1301249 Sbw1_m splenomegaly-NZB x NZW 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:7937857 1301249 Sbw1_m splenomegaly-NZB x NZW 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7937857 1301249 Sbw1_m splenomegaly-NZB x NZW 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7937857 1301251 Scc3_m colon tumor susceptibility 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8944029 1301251 Scc3_m colon tumor susceptibility 3 (mouse) qtl MP:0002020 increased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:14562056 1301252 Etohc3_m ethanol consumption 3 (mouse) qtl MP:0001425 abnormal alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:7978106 1301252 Etohc3_m ethanol consumption 3 (mouse) qtl MP:0001425 abnormal alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:9880656 1301252 Etohc3_m ethanol consumption 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9880656 1301253 Skmw2_m skeletal muscle weight 2 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:14679300 1301253 Skmw2_m skeletal muscle weight 2 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14679300 1301253 Skmw2_m skeletal muscle weight 2 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:14679300 1301253 Skmw2_m skeletal muscle weight 2 (mouse) qtl MP:0009423 increased extensor digitorum longus weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 1301254 Skts11_m skin tumor susceptibility 11 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1301254 Skts11_m skin tumor susceptibility 11 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:10611333 1301254 Skts11_m skin tumor susceptibility 11 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1301255 Cd4ts6_m CD4 T cell subset 6 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12595899 1301255 Cd4ts6_m CD4 T cell subset 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301255 Cd4ts6_m CD4 T cell subset 6 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301256 Skmw1_m skeletal muscle weight 1 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:14679300 1301256 Skmw1_m skeletal muscle weight 1 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14679300 1301256 Skmw1_m skeletal muscle weight 1 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:14679300 1301256 Skmw1_m skeletal muscle weight 1 (mouse) qtl MP:0009421 increased gastrocnemius weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 1301257 Yaa3_m Y-linked autoimmune acceleration 3 (mouse) qtl MP:0001859 kidney inflammation IAGP N RGD:5509061 20111116 MGI PMID:9743333 1301257 Yaa3_m Y-linked autoimmune acceleration 3 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9743333 1301257 Yaa3_m Y-linked autoimmune acceleration 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9743333 1301259 Hcs2_m hepatocarcinogenesis susceptibility 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8417808 1301259 Hcs2_m hepatocarcinogenesis susceptibility 2 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:8417808 1301259 Hcs2_m hepatocarcinogenesis susceptibility 2 (mouse) qtl MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8417808 1301260 Exen1_m exencephaly 1 (mouse) qtl MP:0000914 exencephaly IAGP N RGD:5509061 20111116 MGI PMID:12856282 1301260 Exen1_m exencephaly 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11598925 1301261 Hdl4_m high density lipoprotein (HDL) level 4 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:11108726 1301261 Hdl4_m high density lipoprotein (HDL) level 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11108726 1301262 Gasa3_m gastritis type A susceptibility locus 3 (mouse) qtl MP:0001873 stomach inflammation IAGP N RGD:5509061 20111116 MGI PMID:11862406 1301262 Gasa3_m gastritis type A susceptibility locus 3 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11862406 1301262 Gasa3_m gastritis type A susceptibility locus 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11862406 1301263 Szs11_m seizure susceptibility 11 (mouse) qtl MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20111116 MGI PMID:11472065 1301263 Szs11_m seizure susceptibility 11 (mouse) qtl MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20111116 MGI PMID:17698926 1301263 Szs11_m seizure susceptibility 11 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1301263 Szs11_m seizure susceptibility 11 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1301264 Cocia6_m cocaine induced activation 6 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12777963 1301264 Cocia6_m cocaine induced activation 6 (mouse) qtl MP:0008911 induced hyperactivity IAGP N RGD:5509061 20220421 MGI PMID:12777963 1301264 Cocia6_m cocaine induced activation 6 (mouse) qtl MP:0020871 abnormal locomotor response to cocaine IAGP N RGD:5509061 20220421 MGI PMID:12777963 1301265 Idd21_m insulin dependent diabetes susceptibility 21 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:12856285 1301265 Idd21_m insulin dependent diabetes susceptibility 21 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12856285 1301266 Lmr4_m leishmaniasis resistance 4 (mouse) qtl MP:0001212 skin lesions IAGP N RGD:5509061 20111116 MGI PMID:11196712 1301266 Lmr4_m leishmaniasis resistance 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11196712 1301266 Lmr4_m leishmaniasis resistance 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11196712 1301266 Lmr4_m leishmaniasis resistance 4 (mouse) qtl MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20111116 MGI PMID:11196712 1301266 Lmr4_m leishmaniasis resistance 4 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11196712 1301267 Bcmd2_m B cell maturation defect 2 (mouse) qtl MP:0000324 increased mast cell number IAGP N RGD:5509061 20111116 MGI PMID:11862404 1301267 Bcmd2_m B cell maturation defect 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11862404 1301267 Bcmd2_m B cell maturation defect 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11862404 1301268 Bmd14_m bone mineral density 14 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11450694 1301268 Bmd14_m bone mineral density 14 (mouse) qtl MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:11450694 1301268 Bmd14_m bone mineral density 14 (mouse) qtl MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20220922 MGI PMID:11450694 1301269 Sluc12_m susceptibility to lung cancer 12 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9809979 1301269 Sluc12_m susceptibility to lung cancer 12 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301269 Sluc12_m susceptibility to lung cancer 12 (mouse) qtl MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301270 Dloc1_m duration of locomotor activity 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14694905 1301270 Dloc1_m duration of locomotor activity 1 (mouse) qtl MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:14694905 1301271 Datd_m dopamine transporter density (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11454925 1301271 Datd_m dopamine transporter density (mouse) qtl MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20111116 MGI PMID:11454925 1301272 Cfsw1_m cystic fibrosis survival to weaning 1 (mouse) qtl MP:0002082 postnatal lethality IAGP N RGD:5509061 20111116 MGI PMID:12441405 1301272 Cfsw1_m cystic fibrosis survival to weaning 1 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12441405 1301273 Wt6q1_m body weight (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:10353911 1301273 Wt6q1_m body weight (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1301274 Lmr9_m leishmaniasis resistance 9 (mouse) qtl MP:0002492 decreased IgE level IAGP N RGD:5509061 20111116 MGI PMID:12058253 1301274 Lmr9_m leishmaniasis resistance 9 (mouse) qtl MP:0002497 increased IgE level IAGP N RGD:5509061 20111116 MGI PMID:12058253 1301274 Lmr9_m leishmaniasis resistance 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1301274 Lmr9_m leishmaniasis resistance 9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1301274 Lmr9_m leishmaniasis resistance 9 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:12058253 1301274 Lmr9_m leishmaniasis resistance 9 (mouse) qtl MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20111116 MGI PMID:16511555 1301275 Sle10_m systematic lupus erythematosus susceptibility 10 (mouse) qtl MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20111116 MGI PMID:10693874 1301275 Sle10_m systematic lupus erythematosus susceptibility 10 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10693874 1301276 Tswt_m testis weight (mouse) qtl MP:0004852 decreased testis weight IAGP N RGD:5509061 20111116 MGI PMID:15020476 1301276 Tswt_m testis weight (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15020476 1301276 Tswt_m testis weight (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15020476 1301277 nctm1_m Nakano cataract modifier 1 (mouse) qtl MP:0001304 cataract IAGP N RGD:5509061 20111116 MGI PMID:12470976 1301277 nctm1_m Nakano cataract modifier 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12470976 1301278 Bdln1_m body length 1 (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20111116 MGI PMID:8833234 1301278 Bdln1_m body length 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8833234 1301279 Obq4_m obesity QTL 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9268627|PMID:11210195 1301279 Obq4_m obesity QTL 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:9268627 1301279 Obq4_m obesity QTL 4 (mouse) qtl MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:9268627 1301281 Frp2_m free running period 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11381025 1301281 Frp2_m free running period 2 (mouse) qtl MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:11381025 1301282 Ses1_m salmonella enteritidis susceptibility 1 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:12058254 1301282 Ses1_m salmonella enteritidis susceptibility 1 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:15973461 1301283 Alcw3_m alcohol withdrawal 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12893462|PMID:16436183|PMID:12925894 1301283 Alcw3_m alcohol withdrawal 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12893462|PMID:16436183|PMID:12925894 1301283 Alcw3_m alcohol withdrawal 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:12893462 1301283 Alcw3_m alcohol withdrawal 3 (mouse) qtl MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20111116 MGI PMID:12893462 1301283 Alcw3_m alcohol withdrawal 3 (mouse) qtl MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20111116 MGI PMID:12893462 1301284 Cosz3_m cocaine seizure 3 (mouse) qtl MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20111116 MGI PMID:10734168 1301284 Cosz3_m cocaine seizure 3 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10734168 1301284 Cosz3_m cocaine seizure 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10734168 1301287 Feml2_m femur length in high growth mice 2 (mouse) qtl MP:0001258 decreased body length IAGP N RGD:5509061 20111116 MGI PMID:16670015 1301287 Feml2_m femur length in high growth mice 2 (mouse) qtl MP:0004348 long femur IAGP N RGD:5509061 20111116 MGI PMID:11309659 1301287 Feml2_m femur length in high growth mice 2 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301287 Feml2_m femur length in high growth mice 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301287 Feml2_m femur length in high growth mice 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301288 Bw13_m body weight QTL 13 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11116089 1301288 Bw13_m body weight QTL 13 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089 1301289 Axtofa1_m anxiety-open field activity 1 (mouse) qtl MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20111116 MGI PMID:14990867 1301289 Axtofa1_m anxiety-open field activity 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11454769|PMID:14990867 1301289 Axtofa1_m anxiety-open field activity 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160422 MGI Created by mouse qtl pipeline PMID:11454769 1301290 Smgd1_m submucosal gland distribution 1 (mouse) qtl MP:0002277 abnormal respiratory mucosa morphology IAGP N RGD:5509061 20111116 MGI PMID:11210181 1301290 Smgd1_m submucosal gland distribution 1 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11210181 1301292 Cfbw2_m cystic fibrosis body weight 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:12461646 1301292 Cfbw2_m cystic fibrosis body weight 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12461646 1301293 Pgia13_m proteoglycan induced arthritis 13 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:11046062 1301293 Pgia13_m proteoglycan induced arthritis 13 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15084914|PMID:11046062 1301293 Pgia13_m proteoglycan induced arthritis 13 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150925 MGI Created by mouse qtl pipeline PMID:11046062 1301293 Pgia13_m proteoglycan induced arthritis 13 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15084914|PMID:11046062 1301293 Pgia13_m proteoglycan induced arthritis 13 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20150925 MGI Created by mouse qtl pipeline PMID:11046062 1301294 Hrtfm5_m heart failure modifier 5 (mouse) qtl MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20111116 MGI PMID:14519689 1301294 Hrtfm5_m heart failure modifier 5 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14519689 1301294 Hrtfm5_m heart failure modifier 5 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14519689 1301295 Prdt1_m prion disease incubation time 1 (mouse) qtl MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20111116 MGI PMID:12481985 1301295 Prdt1_m prion disease incubation time 1 (mouse) qtl MP:0005364 increased susceptibility to prion infection IAGP N RGD:5509061 20111116 MGI PMID:12481985 1301295 Prdt1_m prion disease incubation time 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11353827 1301298 Pgia4_m proteoglycan induced arthritis 4 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:10615997 1301298 Pgia4_m proteoglycan induced arthritis 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10615997|PMID:15084914 1301298 Pgia4_m proteoglycan induced arthritis 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:10615997 1301299 Sluc23_m susceptibility to lung cancer 23 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1301299 Sluc23_m susceptibility to lung cancer 23 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301299 Sluc23_m susceptibility to lung cancer 23 (mouse) qtl MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301300 Lbm3_m lean body mass 3 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:12185457 1301300 Lbm3_m lean body mass 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12185457 1301301 Sle1_m systemic lupus erythmatosus susceptibility 1 (mouse) qtl MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20111116 MGI PMID:16002707 1301301 Sle1_m systemic lupus erythmatosus susceptibility 1 (mouse) qtl MP:0002493 increased IgG level IAGP N RGD:5509061 20111116 MGI PMID:15986357 1301301 Sle1_m systemic lupus erythmatosus susceptibility 1 (mouse) qtl MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:15986357 1301301 Sle1_m systemic lupus erythmatosus susceptibility 1 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:15986357 1301301 Sle1_m systemic lupus erythmatosus susceptibility 1 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:15986357 1301301 Sle1_m systemic lupus erythmatosus susceptibility 1 (mouse) qtl MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:16002707 1301301 Sle1_m systemic lupus erythmatosus susceptibility 1 (mouse) qtl MP:0005014 increased B cell number IAGP N RGD:5509061 20111116 MGI PMID:15986357 1301301 Sle1_m systemic lupus erythmatosus susceptibility 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8661718|PMID:16002707 1301301 Sle1_m systemic lupus erythmatosus susceptibility 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8661718|PMID:16002707 1301301 Sle1_m systemic lupus erythmatosus susceptibility 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8661718|PMID:16002707 1301301 Sle1_m systemic lupus erythmatosus susceptibility 1 (mouse) qtl MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20111116 MGI PMID:15986357 1301301 Sle1_m systemic lupus erythmatosus susceptibility 1 (mouse) qtl MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20111116 MGI PMID:18607347 1301301 Sle1_m systemic lupus erythmatosus susceptibility 1 (mouse) qtl MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20111116 MGI PMID:18607347 1301303 Alcp4_m alcohol preference locus 4 (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:10443995 1301303 Alcp4_m alcohol preference locus 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9880657 1301304 Hrq3_m heart rate quantitative locus 3 (mouse) qtl MP:0002626 increased heart rate IAGP N RGD:5509061 20111116 MGI PMID:12118100 1301304 Hrq3_m heart rate quantitative locus 3 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118100 1301307 Phospq1_m phospholipid QTL 1 (mouse) qtl MP:0001547 abnormal lipid level IAGP N RGD:5509061 20111116 MGI PMID:11109545 1301307 Phospq1_m phospholipid QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11109545 1301308 Prdt4_m prion disease incubation time 4 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11353827 1301308 Prdt4_m prion disease incubation time 4 (mouse) qtl MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20111116 MGI PMID:11353827 1301309 Emo1_m emotionality 1 (mouse) qtl MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20111116 MGI PMID:10556431 1301309 Emo1_m emotionality 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10556431 1301310 Tmevd5_m Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 5 (mouse) qtl MP:0000921 demyelination IAGP N RGD:5509061 20111116 MGI PMID:10482543 1301310 Tmevd5_m Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 5 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10482543 1301312 Hsm1_m hereditary spherocytosis modifer 1 (mouse) qtl MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20111116 MGI PMID:15070709 1301312 Hsm1_m hereditary spherocytosis modifer 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15070709 1301313 Pas5a_m pulmonary adenoma susceptibility 5a (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11195459|PMID:8630506 1301313 Pas5a_m pulmonary adenoma susceptibility 5a (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20160219 MGI Created by mouse qtl pipeline PMID:11195459 1301313 Pas5a_m pulmonary adenoma susceptibility 5a (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11195459|PMID:8630506 1301316 Dntcs1_m dental caries susceptibility 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:14767162 1301316 Dntcs1_m dental caries susceptibility 1 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14767162 1301316 Dntcs1_m dental caries susceptibility 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20170929 MGI Created by mouse qtl pipeline PMID:14767162 1301316 Dntcs1_m dental caries susceptibility 1 (mouse) qtl MP:0030101 carious teeth IAGP N RGD:5509061 20170928 MGI PMID:14767162 1301320 Ots1_m ovarian teratoma susceptibility 1 (mouse) qtl MP:0002016 ovary cyst IAGP N RGD:5509061 20111116 MGI PMID:9044831 1301320 Ots1_m ovarian teratoma susceptibility 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9044831 1301320 Ots1_m ovarian teratoma susceptibility 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9044831 1301320 Ots1_m ovarian teratoma susceptibility 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9044831 1301322 Lbm2_m lean body mass 2 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:12185457 1301322 Lbm2_m lean body mass 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12185457 1301323 Asm2_m autoimmune sialadenitis in MRL mice 2 (mouse) qtl MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20111116 MGI PMID:10616009 1301323 Asm2_m autoimmune sialadenitis in MRL mice 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10616009 1301323 Asm2_m autoimmune sialadenitis in MRL mice 2 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10616009 1301323 Asm2_m autoimmune sialadenitis in MRL mice 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10616009 1301325 Pgia15_m proteoglycan induced arthritis 15 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:11046062 1301325 Pgia15_m proteoglycan induced arthritis 15 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15084914|PMID:11046062 1301325 Pgia15_m proteoglycan induced arthritis 15 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150925 MGI Created by mouse qtl pipeline PMID:11046062 1301325 Pgia15_m proteoglycan induced arthritis 15 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15084914|PMID:11046062 1301325 Pgia15_m proteoglycan induced arthritis 15 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20150925 MGI Created by mouse qtl pipeline PMID:11046062 1301327 Lmr7_m leishmaniasis resistance 7 (mouse) qtl MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20111116 MGI PMID:11196712 1301327 Lmr7_m leishmaniasis resistance 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:11196712 1301327 Lmr7_m leishmaniasis resistance 7 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11196712 1301327 Lmr7_m leishmaniasis resistance 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11196712 1301327 Lmr7_m leishmaniasis resistance 7 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11196712 1301327 Lmr7_m leishmaniasis resistance 7 (mouse) qtl MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20111116 MGI PMID:16511555 1301332 Estq1_m estradiol regulated response QTL 1 (mouse) qtl MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20111116 MGI PMID:9927277 1301332 Estq1_m estradiol regulated response QTL 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9176411 1301333 Mop3_m morphine preference 3 (mouse) qtl MP:0002554 aversion to addictive substance IAGP N RGD:5509061 20111116 MGI PMID:8075641 1301333 Mop3_m morphine preference 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8075641 1301334 Cocia10_m cocaine induced activation 10 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12777963 1301334 Cocia10_m cocaine induced activation 10 (mouse) qtl MP:0008911 induced hyperactivity IAGP N RGD:5509061 20220421 MGI PMID:12777963 1301334 Cocia10_m cocaine induced activation 10 (mouse) qtl MP:0020871 abnormal locomotor response to cocaine IAGP N RGD:5509061 20220421 MGI PMID:12777963 1301335 Axtofa4_m anxiety-open field activity 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11454769 1301337 Cdcs8_m cytokine deficiency colitis susceptibility 8 (mouse) qtl MP:0001858 intestinal inflammation IAGP N RGD:5509061 20111116 MGI PMID:12213197 1301337 Cdcs8_m cytokine deficiency colitis susceptibility 8 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12213197 1301337 Cdcs8_m cytokine deficiency colitis susceptibility 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12213197 1301338 Lmr1_m leishmaniasis resistance 1 (mouse) qtl MP:0001792 impaired wound healing IAGP N RGD:5509061 20111116 MGI PMID:16223880 1301338 Lmr1_m leishmaniasis resistance 1 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:16223880 1301338 Lmr1_m leishmaniasis resistance 1 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:9151907 1301338 Lmr1_m leishmaniasis resistance 1 (mouse) qtl MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:10508279 1301338 Lmr1_m leishmaniasis resistance 1 (mouse) qtl MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:9151907 1301338 Lmr1_m leishmaniasis resistance 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9151907 1301338 Lmr1_m leishmaniasis resistance 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9151907 1301339 Hdlq15_m HDL QTL 15 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14592847 1301339 Hdlq15_m HDL QTL 15 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14592847 1301339 Hdlq15_m HDL QTL 15 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18772481 1301339 Hdlq15_m HDL QTL 15 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592847|PMID:18048852 1301339 Hdlq15_m HDL QTL 15 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:14592847 1301340 Bw16_m body weight QTL 16 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11116089 1301340 Bw16_m body weight QTL 16 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089 1301344 Lith1_m lithogenic gene 1 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:11074014 1301344 Lith1_m lithogenic gene 1 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11074014|PMID:12810825 1301344 Lith1_m lithogenic gene 1 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20150717 MGI Created by mouse qtl pipeline PMID:11074014 1301346 Tmevd8_m Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 8 (mouse) qtl MP:0000921 demyelination IAGP N RGD:5509061 20111116 MGI PMID:12663542 1301346 Tmevd8_m Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 8 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12663542 1301347 Fpli_m fasting plasma insulin (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:12439655 1301347 Fpli_m fasting plasma insulin (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12439655 1301349 Pgia26_m proteoglycan induced arthritis 26 (mouse) qtl MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:12794840 1301349 Pgia26_m proteoglycan induced arthritis 26 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:12794840 1301349 Pgia26_m proteoglycan induced arthritis 26 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:12794840 1301349 Pgia26_m proteoglycan induced arthritis 26 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12794840 1301349 Pgia26_m proteoglycan induced arthritis 26 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12794840 1301350 Nidd4k_m Nidd4 on KK-A (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:12115031 1301350 Nidd4k_m Nidd4 on KK-A (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115031 1301351 Obq6_m obesity QTL 6 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10501964 1301351 Obq6_m obesity QTL 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:10501964 1301351 Obq6_m obesity QTL 6 (mouse) qtl MP:0010024 increased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:10501964 1301352 Bis4_m beta-carboline induced seizures 4 (mouse) qtl MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20111116 MGI PMID:10234005 1301352 Bis4_m beta-carboline induced seizures 4 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10234005 1301352 Bis4_m beta-carboline induced seizures 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10234005 1301353 Lbw6_m lupus NZB x NZW 6 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:7937857 1301353 Lbw6_m lupus NZB x NZW 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7937857 1301354 Hcs4_m hepatocarcinogenesis susceptibility 4 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7829059 1301354 Hcs4_m hepatocarcinogenesis susceptibility 4 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:7829059 1301354 Hcs4_m hepatocarcinogenesis susceptibility 4 (mouse) qtl MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20111116 MGI PMID:7829059 1301355 Hipp2_m hippocampal weight 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11331379 1301355 Hipp2_m hippocampal weight 2 (mouse) qtl MP:0008282 enlarged hippocampus IAGP N RGD:5509061 20111116 MGI PMID:11331379 1301356 Idd8_m insulin dependent diabetes susceptibility 8 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:8401590 1301356 Idd8_m insulin dependent diabetes susceptibility 8 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8401590 1301357 Hdlq32_m HDL QTL 32 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14993241 1301357 Hdlq32_m HDL QTL 32 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14993241 1301358 Eae20_m experimental allergic encephalomyelitis 20 (mouse) qtl MP:0000921 demyelination IAGP N RGD:5509061 20111116 MGI PMID:10934166 1301358 Eae20_m experimental allergic encephalomyelitis 20 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10934166 1301360 Stheal1_m soft tissue heal 1 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:11731492 1301360 Stheal1_m soft tissue heal 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11731492 1301361 Idd14_m insulin dependent diabetes susceptibility 14 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:7556956 1301361 Idd14_m insulin dependent diabetes susceptibility 14 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17982459|PMID:7556956 1301362 Prnr1_m prion resistance 1 (mouse) qtl MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20111116 MGI PMID:14704188 1301362 Prnr1_m prion resistance 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14704188 1301364 Lith14_m lithogenic gene 14 (mouse) qtl MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20111116 MGI PMID:12837957 1301364 Lith14_m lithogenic gene 14 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12837957|PMID:16151694 1301364 Lith14_m lithogenic gene 14 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12837957|PMID:16151694 1301364 Lith14_m lithogenic gene 14 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150724 MGI Created by mouse qtl pipeline PMID:12837957 1301365 Ap5q_m alcohol preference 5 QTL (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:9726281 1301365 Ap5q_m alcohol preference 5 QTL (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9726281 1301368 Par2_m pulmonary adenoma resistance 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11195460|PMID:11494126|PMID:9331067 1301368 Par2_m pulmonary adenoma resistance 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20160729 MGI Created by mouse qtl pipeline PMID:11195460|PMID:11494126 1301368 Par2_m pulmonary adenoma resistance 2 (mouse) qtl MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20111116 MGI PMID:11494126 1301368 Par2_m pulmonary adenoma resistance 2 (mouse) qtl MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23955086 1301368 Par2_m pulmonary adenoma resistance 2 (mouse) qtl MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20111116 MGI PMID:8895504 1301368 Par2_m pulmonary adenoma resistance 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11195460|PMID:11494126|PMID:9331067 1301368 Par2_m pulmonary adenoma resistance 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20160729 MGI Created by mouse qtl pipeline PMID:11195460|PMID:11494126 1301368 Par2_m pulmonary adenoma resistance 2 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:11195460|PMID:11494126 1301369 Im4_m immunoregulatory 4 (mouse) qtl MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20111116 MGI PMID:8962125 1301369 Im4_m immunoregulatory 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8962125 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11178736 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180621 MGI PMID:20388922 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20180621 MGI PMID:20388922 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0002833 increased heart weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180621 MGI PMID:20388922 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180621 MGI PMID:20388922 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20180621 MGI PMID:20388922 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 1301370 Adip1_m adiposity 1 (mouse) qtl MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 1301373 Vent2_m ventricular size 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12746874 1301373 Vent2_m ventricular size 2 (mouse) qtl MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20140220 MGI PMID:12746874 1301375 Tria4_m T-cell receptor induced activation 4 (mouse) qtl MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20111116 MGI PMID:10384038 1301375 Tria4_m T-cell receptor induced activation 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10384038 1301375 Tria4_m T-cell receptor induced activation 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:10384038 1301376 Etohc1_m ethanol consumption 1 (mouse) qtl MP:0001425 abnormal alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:9880656 1301376 Etohc1_m ethanol consumption 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9880656 1301377 Mprf_m maternal performance (mouse) qtl MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20111116 MGI PMID:12454078 1301377 Mprf_m maternal performance (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12454078 1301378 Hpdty_m hindlimb polydactyly (mouse) qtl MP:0000562 polydactyly IAGP N RGD:5509061 20111116 MGI PMID:15170224 1301378 Hpdty_m hindlimb polydactyly (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15170224 1301379 Sials_m sialoadenitis susceptibility (mouse) qtl MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20111116 MGI PMID:10980337 1301379 Sials_m sialoadenitis susceptibility (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10980337 1301379 Sials_m sialoadenitis susceptibility (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10980337 1301379 Sials_m sialoadenitis susceptibility (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10980337 1301380 Cia8_m collagen induced arthritis QTL 8 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10453039 1301380 Cia8_m collagen induced arthritis QTL 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10453039|PMID:15761851 1301380 Cia8_m collagen induced arthritis QTL 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:10453039 1301380 Cia8_m collagen induced arthritis QTL 8 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10453039|PMID:15761851 1301381 Bomb1_m bone marrow pre-B 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10363979 1301381 Bomb1_m bone marrow pre-B 1 (mouse) qtl MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20111116 MGI PMID:10363979 1301381 Bomb1_m bone marrow pre-B 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10363979 1301381 Bomb1_m bone marrow pre-B 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10363979 1301381 Bomb1_m bone marrow pre-B 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10363979 1301381 Bomb1_m bone marrow pre-B 1 (mouse) qtl MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20131226 MGI PMID:10363979 1301382 Arvm2_m autoimmune renal vasculitis 2 (mouse) qtl MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20111116 MGI PMID:10940892 1301382 Arvm2_m autoimmune renal vasculitis 2 (mouse) qtl MP:0001864 vascular inflammation IAGP N RGD:5509061 20111116 MGI PMID:10940892 1301382 Arvm2_m autoimmune renal vasculitis 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10940892 1301382 Arvm2_m autoimmune renal vasculitis 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10940892 1301383 Aem2_m anti-erythrocyte autoantibody modifier 2 (mouse) qtl MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:10607744 1301383 Aem2_m anti-erythrocyte autoantibody modifier 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10607744 1301385 Radpf2_m radiation pulmonary fibrosis 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:12097289 1301385 Radpf2_m radiation pulmonary fibrosis 2 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12097289 1301385 Radpf2_m radiation pulmonary fibrosis 2 (mouse) qtl MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20111116 MGI PMID:12097289 1301386 Sysbp1_m systolic blood pressure 1 (mouse) qtl MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20111116 MGI PMID:10523337 1301386 Sysbp1_m systolic blood pressure 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10523337 1301387 Chol8_m cholesterol 8 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14701919 1301387 Chol8_m cholesterol 8 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14701919 1301388 Hdlq21_m HDL QTL 21 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14993241 1301388 Hdlq21_m HDL QTL 21 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18772481|PMID:14993241 1301388 Hdlq21_m HDL QTL 21 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:14993241 1301390 Hpnr6_m Heligmosomoides polygyrus nematode resistance 6 (mouse) qtl MP:0002497 increased IgE level IAGP N RGD:5509061 20111116 MGI PMID:14507332 1301392 Eae3_m susceptibility to experimental allergic encephalomyelitis 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7545492|PMID:8757345 1301393 Dyscalc3_m dystrophic cardiac calcinosis 3 (mouse) qtl MP:0002838 decreased susceptibility to dystrophic cardiac calcinosis IAGP N RGD:5509061 20111116 MGI PMID:11526197 1301393 Dyscalc3_m dystrophic cardiac calcinosis 3 (mouse) qtl MP:0002839 increased susceptibility to dystrophic cardiac calcinosis IAGP N RGD:5509061 20111116 MGI PMID:11526197 1301393 Dyscalc3_m dystrophic cardiac calcinosis 3 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11526197 1301394 Eae11_m susceptibility to experimental allergic encephalomyelitis 11 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517969|PMID:10072563 1301394 Eae11_m susceptibility to experimental allergic encephalomyelitis 11 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:10072563 1301394 Eae11_m susceptibility to experimental allergic encephalomyelitis 11 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517969|PMID:10072563 1301394 Eae11_m susceptibility to experimental allergic encephalomyelitis 11 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150717 MGI Created by mouse qtl pipeline PMID:10072563 1301395 Wt10q3_m body weight (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:10353911 1301395 Wt10q3_m body weight (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1301396 Apmt2_m accelerator of polyoma-induced mammary tumors 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11003704 1301396 Apmt2_m accelerator of polyoma-induced mammary tumors 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:11003704 1301396 Apmt2_m accelerator of polyoma-induced mammary tumors 2 (mouse) qtl MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:11003704 1301396 Apmt2_m accelerator of polyoma-induced mammary tumors 2 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:11003704 1301397 Amp2_m amplitude of circadian rhythm 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11381025 1301397 Amp2_m amplitude of circadian rhythm 2 (mouse) qtl MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:11381025 1301398 Rapop3_m radiation-induced apoptosis 3 (mouse) qtl MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20111116 MGI PMID:8825642 1301398 Rapop3_m radiation-induced apoptosis 3 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8825642 1301399 Cpfd3_m cerebellum pattern fissures (mouse) qtl MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20111116 MGI PMID:11529272 1301399 Cpfd3_m cerebellum pattern fissures (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11529272 1301400 Lmr13_m leishmaniasis resistance 13 (mouse) qtl MP:0001212 skin lesions IAGP N RGD:5509061 20111116 MGI PMID:12058253 1301400 Lmr13_m leishmaniasis resistance 13 (mouse) qtl MP:0002492 decreased IgE level IAGP N RGD:5509061 20111116 MGI PMID:12058253 1301400 Lmr13_m leishmaniasis resistance 13 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1301400 Lmr13_m leishmaniasis resistance 13 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1301400 Lmr13_m leishmaniasis resistance 13 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:12058253 1301400 Lmr13_m leishmaniasis resistance 13 (mouse) qtl MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20111116 MGI PMID:16511555 1301400 Lmr13_m leishmaniasis resistance 13 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058253 1301401 Odsm1_m ocular degeneration with sex reversal modifier 1 (mouse) qtl MP:0001939 secondary sex reversal IAGP N RGD:5509061 20111116 MGI PMID:12588798 1301401 Odsm1_m ocular degeneration with sex reversal modifier 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12588798 1301402 Ap2q_m alcohol preference 2 QTL (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:11523702 1301402 Ap2q_m alcohol preference 2 QTL (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:9726281 1301402 Ap2q_m alcohol preference 2 QTL (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9726281 1301404 Sbmd4_m spinal bone mineral density 4 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:10780854 1301404 Sbmd4_m spinal bone mineral density 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10780854 1301405 Etohr_m ethanol response acute (mouse) qtl MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20111116 MGI PMID:9880575 1301405 Etohr_m ethanol response acute (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9880575 1301405 Etohr_m ethanol response acute (mouse) qtl MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20111116 MGI PMID:9880575 1301407 Rapop2_m radiation-induced apoptosis 2 (mouse) qtl MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20111116 MGI PMID:8825642 1301407 Rapop2_m radiation-induced apoptosis 2 (mouse) qtl MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20111116 MGI PMID:9545495 1301407 Rapop2_m radiation-induced apoptosis 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9545495|PMID:9367689 1301407 Rapop2_m radiation-induced apoptosis 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:9545495 1301408 Lore8_m loss of righting induced by ethanol 8 (mouse) qtl MP:0001523 impaired righting response IAGP N RGD:5509061 20111116 MGI PMID:11003198 1301408 Lore8_m loss of righting induced by ethanol 8 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11003198 1301410 Cd8mts6_m CD8 memory T cell subset 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301410 Cd8mts6_m CD8 memory T cell subset 6 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301410 Cd8mts6_m CD8 memory T cell subset 6 (mouse) qtl MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20111116 MGI PMID:12595899 1301411 Pitm1_m prion incubation time 1 (mouse) qtl MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20111116 MGI PMID:11404459 1301411 Pitm1_m prion incubation time 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11404459 1301414 Heal10_m wound healing/regeneration 10 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:12682777 1301414 Heal10_m wound healing/regeneration 10 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12682777 1301417 Ltsd5_m lung tumor shape-determining 5 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517788 1301417 Ltsd5_m lung tumor shape-determining 5 (mouse) qtl MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20111116 MGI PMID:12517788 1301419 Cypr3_m cytokine production 3 (mouse) qtl MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20111116 MGI PMID:9887350 1301419 Cypr3_m cytokine production 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9887350 1301422 Sle11_m systematic lupus erythematosus susceptibility 11 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10693874 1301422 Sle11_m systematic lupus erythematosus susceptibility 11 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:10693874 1301422 Sle11_m systematic lupus erythematosus susceptibility 11 (mouse) qtl MP:0008502 increased IgG3 level IAGP N RGD:5509061 20111116 MGI PMID:10693874 1301424 Skull21_m skull morphology 21 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301424 Skull21_m skull morphology 21 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301424 Skull21_m skull morphology 21 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301426 Desp2_m despair 2 (mouse) qtl MP:0002573 behavioral despair IAGP N RGD:5509061 20111116 MGI PMID:11875023 1301426 Desp2_m despair 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11875023 1301430 Cdcs2_m cytokine deficiency colitis susceptibility 2 (mouse) qtl MP:0001858 intestinal inflammation IAGP N RGD:5509061 20111116 MGI PMID:11707574 1301430 Cdcs2_m cytokine deficiency colitis susceptibility 2 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11707574 1301430 Cdcs2_m cytokine deficiency colitis susceptibility 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11707574 1301432 Hpnr1_m Heligmosomoides polygyrus nematode resistance 1 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:12647241 1301432 Hpnr1_m Heligmosomoides polygyrus nematode resistance 1 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:14507332 1301432 Hpnr1_m Heligmosomoides polygyrus nematode resistance 1 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:16783640 1301435 Trigq1_m triglyceride QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18048852|PMID:14974682 1301435 Trigq1_m triglyceride QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:14974682 1301436 Wg2_m weight gain in high growth mice 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11309659 1301436 Wg2_m weight gain in high growth mice 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301437 Scon1_m sucrose consumption 1 (mouse) qtl MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20111116 MGI PMID:9250857 1301437 Scon1_m sucrose consumption 1 (mouse) qtl MP:0005394 taste/olfaction phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9250857 1301438 Ltsd2_m lung tumor shape-determining 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517788 1301438 Ltsd2_m lung tumor shape-determining 2 (mouse) qtl MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20111116 MGI PMID:12517788 1301439 Morph2_m morphine antinociception 2 (mouse) qtl MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20111116 MGI PMID:11420618 1301439 Morph2_m morphine antinociception 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11420618 1301439 Morph2_m morphine antinociception 2 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11420618 1301441 Skull11_m skull morphology 11 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301441 Skull11_m skull morphology 11 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301441 Skull11_m skull morphology 11 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301442 Pltpq1_m phospholipid transfer protein activity QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592843 1301442 Pltpq1_m phospholipid transfer protein activity QTL 1 (mouse) qtl MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20111116 MGI PMID:14592843 1301443 Mopkd2_m modifier of polycystic kidney disease progression 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9329956 1301443 Mopkd2_m modifier of polycystic kidney disease progression 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9329956 1301443 Mopkd2_m modifier of polycystic kidney disease progression 2 (mouse) qtl MP:0008528 polycystic kidney IAGP N RGD:5509061 20111116 MGI PMID:9329956 1301445 Listr2_m listeriosis resistance 2 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:11242105 1301445 Listr2_m listeriosis resistance 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11242105 1301446 Elsgp4_m elevated serum gp70 4 (mouse) qtl MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20111116 MGI PMID:15067091 1301446 Elsgp4_m elevated serum gp70 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15067091 1301447 Fembm3_m femoral bone morphometry 3 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11518254 1301447 Fembm3_m femoral bone morphometry 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11518254 1301447 Fembm3_m femoral bone morphometry 3 (mouse) qtl MP:0030823 increased femur size IAGP N RGD:5509061 20181018 MGI PMID:11518254 1301449 Cia10_m collagen induced arthritis 10 (mouse) qtl MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:9808201 1301449 Cia10_m collagen induced arthritis 10 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9808201 1301450 Bpq6_m blood pressure QTL 6 (mouse) qtl MP:0000231 hypertension IAGP N RGD:5509061 20111116 MGI PMID:11161799 1301450 Bpq6_m blood pressure QTL 6 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11161799|PMID:12118100 1301450 Bpq6_m blood pressure QTL 6 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20160422 MGI Created by mouse qtl pipeline PMID:11161799 1301451 Ath16_m atherosclerosis 16 (mouse) qtl MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20111116 MGI PMID:11973313 1301451 Ath16_m atherosclerosis 16 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11973313 1301452 Elsgp1_m elevated serum gp70 1 (mouse) qtl MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20111116 MGI PMID:10903778 1301452 Elsgp1_m elevated serum gp70 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15067091|PMID:10903778 1301452 Elsgp1_m elevated serum gp70 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150703 MGI Created by mouse qtl pipeline PMID:10903778 1301454 Eae5_m susceptibility to experimental allergic encephalomyelitis 5 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:9712054 1301454 Eae5_m susceptibility to experimental allergic encephalomyelitis 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9712054 1301455 Bmd3_m bone mineral density 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12568393|PMID:10556421 1301455 Bmd3_m bone mineral density 3 (mouse) qtl MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:12568393 1301456 Adip5_m adiposity 5 (mouse) qtl MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11178736 1301456 Adip5_m adiposity 5 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12856282|PMID:11178736 1301456 Adip5_m adiposity 5 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:11178736 1301456 Adip5_m adiposity 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12856282|PMID:11178736 1301457 Cfsw2_m cystic fibrosis survival to weaning 2 (mouse) qtl MP:0002082 postnatal lethality IAGP N RGD:5509061 20111116 MGI PMID:12441405 1301457 Cfsw2_m cystic fibrosis survival to weaning 2 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12441405 1301458 Skts8_m skin tumor susceptibility 8 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1301458 Skts8_m skin tumor susceptibility 8 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:10611333 1301458 Skts8_m skin tumor susceptibility 8 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1301460 C10bw6_m castaneus 10 week body weight 6 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:11003694 1301460 C10bw6_m castaneus 10 week body weight 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11003694 1301461 Chol9_m cholesterol 9 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14701919 1301461 Chol9_m cholesterol 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14701919 1301462 Nhdlq2_m non-HDL QTL 2 (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14701919 1301462 Nhdlq2_m non-HDL QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14701919 1301463 Szs5_m seizure susceptibility 5 (mouse) qtl MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20111116 MGI PMID:10436030 1301463 Szs5_m seizure susceptibility 5 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10436030 1301463 Szs5_m seizure susceptibility 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10436030 1301466 T2dm2_m type 2 diabetes mellitus 2 (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:11078464 1301466 T2dm2_m type 2 diabetes mellitus 2 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:11078464 1301466 T2dm2_m type 2 diabetes mellitus 2 (mouse) qtl MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:16682971 1301466 T2dm2_m type 2 diabetes mellitus 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11078464 1301468 Eye1_m eye weight 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10102277 1301469 Cara2_m carcass ash in high growth mice 2 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:11309659 1301469 Cara2_m carcass ash in high growth mice 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301470 Vmbic3_m ventral midbrain iron content 3 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14744041 1301470 Vmbic3_m ventral midbrain iron content 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14744041 1301470 Vmbic3_m ventral midbrain iron content 3 (mouse) qtl MP:0020365 increased brain iron level IAGP N RGD:5509061 20161020 MGI PMID:14744041 1301471 Obq2_m obesity QTL 2 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:8786140 1301471 Obq2_m obesity QTL 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8786140 1301472 Pain1_m pain 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11427320|PMID:15979798 1301472 Pain1_m pain 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11427320|PMID:15979798 1301473 Triglq1_m triglyceride QTL 1 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:11109545 1301473 Triglq1_m triglyceride QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11109545 1301475 Tnbs1_m tri-nitrobenzene sulfonic acid susceptible 1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301475 Tnbs1_m tri-nitrobenzene sulfonic acid susceptible 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301475 Tnbs1_m tri-nitrobenzene sulfonic acid susceptible 1 (mouse) qtl MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20111116 MGI PMID:12145808 1301477 Rencd_m renal cystic disease severity (mouse) qtl MP:0003675 kidney cyst IAGP N RGD:5509061 20111116 MGI PMID:10864581 1301477 Rencd_m renal cystic disease severity (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10864581 1301477 Rencd_m renal cystic disease severity (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:10864581 1301478 Eae26_m susceptibility to experimental allergic encephalomyelitis 26 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:11751755 1301478 Eae26_m susceptibility to experimental allergic encephalomyelitis 26 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11751755 1301479 Sluc1_m susceptibility to lung cancer 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20160222 MGI Created by mouse qtl pipeline PMID:11584065 1301479 Sluc1_m susceptibility to lung cancer 1 (mouse) qtl MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20160225 MGI PMID:11584065 1301480 Pbwg1_m postnatal body weight growth 1 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:11003694 1301480 Pbwg1_m postnatal body weight growth 1 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 1301480 Pbwg1_m postnatal body weight growth 1 (mouse) qtl MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20111116 MGI PMID:15056934 1301480 Pbwg1_m postnatal body weight growth 1 (mouse) qtl MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20111116 MGI PMID:16174331 1301480 Pbwg1_m postnatal body weight growth 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11003694 1301481 Lith11_m lithogenic gene 11 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:12810825 1301481 Lith11_m lithogenic gene 11 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12810825 1301482 Morph1_m morphine antinociception 1 (mouse) qtl MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20111116 MGI PMID:11420618 1301482 Morph1_m morphine antinociception 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11420618 1301482 Morph1_m morphine antinociception 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11420618 1301483 Obq12_m obesity QTL 12 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11210195 1301483 Obq12_m obesity QTL 12 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11210195 1301484 Bwq6_m body weight (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:12856282 1301484 Bwq6_m body weight (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12856282 1301485 Asthm1_m asthma 1 (mouse) qtl MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20111116 MGI PMID:10072427 1301485 Asthm1_m asthma 1 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10072427 1301487 Nociq1_m nociceptive sensitivity inflammatory QTL 1 (mouse) qtl MP:0002735 abnormal chemical nociception IAGP N RGD:5509061 20111116 MGI PMID:11973013 1301487 Nociq1_m nociceptive sensitivity inflammatory QTL 1 (mouse) qtl MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20111116 MGI PMID:11973013 1301487 Nociq1_m nociceptive sensitivity inflammatory QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11973013 1301487 Nociq1_m nociceptive sensitivity inflammatory QTL 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11973013 1301489 Lbm10_m lean body mass 10 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:12185457 1301489 Lbm10_m lean body mass 10 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12185457 1301490 Pltpq2_m phospholipid transfer protein activity QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592843 1301490 Pltpq2_m phospholipid transfer protein activity QTL 2 (mouse) qtl MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20111116 MGI PMID:14592843 1301491 Abbp4_m A/J and C57BL/6 blood pressure 4 (mouse) qtl MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20111116 MGI PMID:14612590 1301491 Abbp4_m A/J and C57BL/6 blood pressure 4 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14612590 1301492 Dbsty3_m diabesity 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11042154 1301492 Dbsty3_m diabesity 3 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:11042154 1301492 Dbsty3_m diabesity 3 (mouse) qtl MP:0005331 insulin resistance IAGP N RGD:5509061 20111116 MGI PMID:11042154 1301492 Dbsty3_m diabesity 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11042154 1301492 Dbsty3_m diabesity 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11042154 1301495 Cocia13_m cocaine induced activation 13 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12777963 1301495 Cocia13_m cocaine induced activation 13 (mouse) qtl MP:0008911 induced hyperactivity IAGP N RGD:5509061 20220421 MGI PMID:12777963 1301495 Cocia13_m cocaine induced activation 13 (mouse) qtl MP:0020871 abnormal locomotor response to cocaine IAGP N RGD:5509061 20220421 MGI PMID:12777963 1301497 Tgls1_m triglyceride level suppressor 1 (mouse) qtl MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:11473059 1301497 Tgls1_m triglyceride level suppressor 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11473059 1301498 Oriq2_m ovulation rate QTL 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301501 Lmr2_m leishmaniasis resistance 2 (mouse) qtl MP:0001792 impaired wound healing IAGP N RGD:5509061 20111116 MGI PMID:16223880 1301501 Lmr2_m leishmaniasis resistance 2 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:16223880 1301501 Lmr2_m leishmaniasis resistance 2 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:9151907 1301501 Lmr2_m leishmaniasis resistance 2 (mouse) qtl MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:9151907 1301501 Lmr2_m leishmaniasis resistance 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9151907 1301501 Lmr2_m leishmaniasis resistance 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9151907 1301502 Eae17_m susceptibility to experimental allergic encephalomyelitis 17 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:10706738 1301502 Eae17_m susceptibility to experimental allergic encephalomyelitis 17 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10706738 1301505 Tir1_m trypanosome infection response 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9171834|PMID:12847546 1301505 Tir1_m trypanosome infection response 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:9171834|PMID:12847546|PMID:8988870 1301505 Tir1_m trypanosome infection response 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150626 MGI Created by mouse qtl pipeline PMID:9171834|PMID:8988870 1301506 Aevm1_m autoimmune extremity vasculitis in MRL mice 1 (mouse) qtl MP:0001864 vascular inflammation IAGP N RGD:5509061 20111116 MGI PMID:12746919 1301506 Aevm1_m autoimmune extremity vasculitis in MRL mice 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12746919 1301506 Aevm1_m autoimmune extremity vasculitis in MRL mice 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12746919 1301507 Actre1_m activity response to ethanol 1 (mouse) qtl MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20111116 MGI PMID:12882366 1301507 Actre1_m activity response to ethanol 1 (mouse) qtl MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20111116 MGI PMID:17143586 1301507 Actre1_m activity response to ethanol 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12882366|PMID:11529277|PMID:17143586 1301507 Actre1_m activity response to ethanol 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20151204 MGI Created by mouse qtl pipeline PMID:11529277|PMID:17143586 1301507 Actre1_m activity response to ethanol 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20151225 MGI Created by mouse qtl pipeline PMID:11529277 1301508 Bulb4_m bulb size 4 (mouse) qtl MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20111116 MGI PMID:11529276 1301508 Bulb4_m bulb size 4 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11529276 1301510 Bbaa13_m B.burgdorferi-associated arthritis 13 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11704805 1301510 Bbaa13_m B.burgdorferi-associated arthritis 13 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11704805 1301513 Idd9_m insulin dependent diabetes susceptibility 9 (mouse) qtl MP:0001869 pancreas inflammation IAGP N RGD:5509061 20111116 MGI PMID:15905556 1301513 Idd9_m insulin dependent diabetes susceptibility 9 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:10933399 1301513 Idd9_m insulin dependent diabetes susceptibility 9 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:7556956 1301513 Idd9_m insulin dependent diabetes susceptibility 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8199406|PMID:15905556|PMID:7556956 1301513 Idd9_m insulin dependent diabetes susceptibility 9 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8199406|PMID:15905556|PMID:7556956 1301513 Idd9_m insulin dependent diabetes susceptibility 9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8199406|PMID:15905556|PMID:7556956 1301514 Rigs1_m radiation induced gastroschisis 1 (mouse) qtl MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20111116 MGI PMID:9880666 1301514 Rigs1_m radiation induced gastroschisis 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9880666 1301515 Fembm1_m femoral bone morphometry 1 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11518254 1301515 Fembm1_m femoral bone morphometry 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11518254 1301515 Fembm1_m femoral bone morphometry 1 (mouse) qtl MP:0030823 increased femur size IAGP N RGD:5509061 20181018 MGI PMID:11518254 1301516 Alan2_m alloantigen response 2 (mouse) qtl MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20111116 MGI PMID:11197689 1301516 Alan2_m alloantigen response 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11197689 1301518 Bbaa5_m B.burgdorferi-associated arthritis 5 (mouse) qtl MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:9916719 1301518 Bbaa5_m B.burgdorferi-associated arthritis 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9916719 1301518 Bbaa5_m B.burgdorferi-associated arthritis 5 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:9916719 1301519 Mbis1_m Mycobacterium bovis-induced systemic lupus erythematosus 1 (mouse) qtl MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:10903779 1301519 Mbis1_m Mycobacterium bovis-induced systemic lupus erythematosus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10903779 1301521 Pas1c_m pulmonary adenoma susceptibility 1c (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9790761 1301521 Pas1c_m pulmonary adenoma susceptibility 1c (mouse) qtl MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20111116 MGI PMID:9790761 1301521 Pas1c_m pulmonary adenoma susceptibility 1c (mouse) qtl MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20111116 MGI PMID:9790761 1301521 Pas1c_m pulmonary adenoma susceptibility 1c (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9790761 1301521 Pas1c_m pulmonary adenoma susceptibility 1c (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9790761 1301523 Ccrs1_m corpus callosum hemisphere surface size 1 (mouse) qtl MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20111116 MGI PMID:9804947 1301523 Ccrs1_m corpus callosum hemisphere surface size 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9804947 1301524 Lmb2_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0000691 enlarged spleen IAGP N RGD:5509061 20111116 MGI PMID:9449705 1301524 Lmb2_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20111116 MGI PMID:9449705 1301524 Lmb2_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:9449705 1301524 Lmb2_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20111116 MGI PMID:17548658 1301524 Lmb2_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9449705 1301524 Lmb2_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9449705 1301524 Lmb2_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9449705 1301524 Lmb2_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9449705 1301525 Lmb1_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0000691 enlarged spleen IAGP N RGD:5509061 20111116 MGI PMID:9449705 1301525 Lmb1_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20111116 MGI PMID:17548658 1301525 Lmb1_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20111116 MGI PMID:9449705 1301525 Lmb1_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:9449705 1301525 Lmb1_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:17548658 1301525 Lmb1_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20111116 MGI PMID:17548658 1301525 Lmb1_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9449705 1301525 Lmb1_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9449705 1301525 Lmb1_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9449705 1301525 Lmb1_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9449705 1301525 Lmb1_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20111116 MGI PMID:17548658 1301527 Vmbic8_m ventral midbrain iron content 8 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14744041 1301527 Vmbic8_m ventral midbrain iron content 8 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14744041 1301527 Vmbic8_m ventral midbrain iron content 8 (mouse) qtl MP:0008807 increased liver iron level IAGP N RGD:5509061 20111116 MGI PMID:14744041 1301528 Loco1_m locomotor activity 1 (mouse) qtl MP:0001399 hyperactivity IAGP N RGD:5509061 20111116 MGI PMID:12226705 1301528 Loco1_m locomotor activity 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12226705 1301529 Nnc1_m neuron number control 1 (mouse) qtl MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20111116 MGI PMID:9412494 1301529 Nnc1_m neuron number control 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9412494 1301529 Nnc1_m neuron number control 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9412494 1301530 Bglu2_m blood glucose level 2 (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:10894496 1301530 Bglu2_m blood glucose level 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10894496 1301532 Scc8_m colon tumor susceptibility 8 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10485458 1301532 Scc8_m colon tumor susceptibility 8 (mouse) qtl MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20111116 MGI PMID:10485458 1301532 Scc8_m colon tumor susceptibility 8 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:10485458 1301534 Idd20_m insulin dependent diabetes susceptibility 20 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11386752 1301535 Pas5b_m pulmonary adenoma susceptibility 5b (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9790761 1301535 Pas5b_m pulmonary adenoma susceptibility 5b (mouse) qtl MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20111116 MGI PMID:9790761 1301535 Pas5b_m pulmonary adenoma susceptibility 5b (mouse) qtl MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20111116 MGI PMID:9790761 1301535 Pas5b_m pulmonary adenoma susceptibility 5b (mouse) qtl MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20111116 MGI PMID:9790761 1301535 Pas5b_m pulmonary adenoma susceptibility 5b (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9790761 1301535 Pas5b_m pulmonary adenoma susceptibility 5b (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9790761 1301536 Pbbcp1_m peripheral blood B cell percentage 1 (mouse) qtl MP:0005014 increased B cell number IAGP N RGD:5509061 20111116 MGI PMID:11781239 1301536 Pbbcp1_m peripheral blood B cell percentage 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11781239 1301536 Pbbcp1_m peripheral blood B cell percentage 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11781239 1301539 Mwq5_m molecular weight of quadriceps QTL 5 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:11116089 1301539 Mwq5_m molecular weight of quadriceps QTL 5 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089 1301540 Axtofa2_m anxiety-open field activity 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11454769|PMID:14990867 1301542 Paam1_m progression of autoimmune arthritis in MRL mice 1 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20111116 MGI PMID:11953986 1301542 Paam1_m progression of autoimmune arthritis in MRL mice 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11953986 1301543 Hypch_m hypercholesterolemia (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12727230 1301543 Hypch_m hypercholesterolemia (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12727230 1301544 Iba3_m induction of brown adipocytes 3 (mouse) qtl MP:0003012 obsolete no phenotypic analysis IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10931824 1301545 Gauc_m glucose area under curve (mouse) qtl MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20111116 MGI PMID:12439655 1301545 Gauc_m glucose area under curve (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12439655 1301548 Idd4_m insulin dependent diabetes susceptibility 4 (mouse) qtl MP:0001869 pancreas inflammation IAGP N RGD:5509061 20111116 MGI PMID:11756344 1301548 Idd4_m insulin dependent diabetes susceptibility 4 (mouse) qtl MP:0001869 pancreas inflammation IAGP N RGD:5509061 20111116 MGI PMID:15905556 1301548 Idd4_m insulin dependent diabetes susceptibility 4 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:11756344 1301548 Idd4_m insulin dependent diabetes susceptibility 4 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:15905556 1301548 Idd4_m insulin dependent diabetes susceptibility 4 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:1675432 1301548 Idd4_m insulin dependent diabetes susceptibility 4 (mouse) qtl MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20111116 MGI PMID:12759418 1301548 Idd4_m insulin dependent diabetes susceptibility 4 (mouse) qtl MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:7789623 1301548 Idd4_m insulin dependent diabetes susceptibility 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1675432|PMID:8661724|PMID:11756344|PMID:7789623|PMID:15905556|PMID:8401590 1301548 Idd4_m insulin dependent diabetes susceptibility 4 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1675432|PMID:8661724|PMID:11756344|PMID:7789623|PMID:15905556|PMID:8401590 1301548 Idd4_m insulin dependent diabetes susceptibility 4 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1675432|PMID:8661724|PMID:11756344|PMID:7789623|PMID:15905556|PMID:8401590 1301548 Idd4_m insulin dependent diabetes susceptibility 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1675432|PMID:8661724|PMID:11756344|PMID:7789623|PMID:15905556|PMID:8401590 1301548 Idd4_m insulin dependent diabetes susceptibility 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1675432|PMID:8661724|PMID:11756344|PMID:7789623|PMID:15905556|PMID:8401590 1301548 Idd4_m insulin dependent diabetes susceptibility 4 (mouse) qtl MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20111116 MGI PMID:12759418 1301549 Bbaa9_m B.burgdorferi-associated arthritis 9 (mouse) qtl MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20111116 MGI PMID:9916719 1301549 Bbaa9_m B.burgdorferi-associated arthritis 9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9916719 1301549 Bbaa9_m B.burgdorferi-associated arthritis 9 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:9916719 1301550 Fembrs2_m femur breaking strength 2 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:11991724 1301550 Fembrs2_m femur breaking strength 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11991724 1301551 Spha1_m sperm head anomaly 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15020476 1301551 Spha1_m sperm head anomaly 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15020476 1301551 Spha1_m sperm head anomaly 1 (mouse) qtl MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20111116 MGI PMID:15020476 1301554 Fatq1_m percent fat (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:10353911 1301554 Fatq1_m percent fat (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1301556 Cd4vts1_m CD4 virgin T cell subset 1 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12595899 1301556 Cd4vts1_m CD4 virgin T cell subset 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301556 Cd4vts1_m CD4 virgin T cell subset 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301557 Bbaa22_m B.burgdorferi-associated arthritis 22 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11704805 1301557 Bbaa22_m B.burgdorferi-associated arthritis 22 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11704805 1301558 Stheal8_m soft tissue heal 8 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:11731492 1301558 Stheal8_m soft tissue heal 8 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:18028142 1301558 Stheal8_m soft tissue heal 8 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11731492 1301559 Bbaa19_m B.burgdorferi-associated arthritis 19 (mouse) qtl MP:0002493 increased IgG level IAGP N RGD:5509061 20111116 MGI PMID:11704805 1301559 Bbaa19_m B.burgdorferi-associated arthritis 19 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11704805 1301559 Bbaa19_m B.burgdorferi-associated arthritis 19 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:11704805 1301560 Siafq1_m stress induced analgesia (mouse) qtl MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20111116 MGI PMID:9315917 1301560 Siafq1_m stress induced analgesia (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9315917 1301561 Chab2_m cholesterol absorption 2 (mouse) qtl MP:0002646 increased intestinal cholesterol absorption IAGP N RGD:5509061 20111116 MGI PMID:11714849 1301561 Chab2_m cholesterol absorption 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11714849 1301561 Chab2_m cholesterol absorption 2 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11714849 1301562 Hwq1_m heart weight quantitative locus 1 (mouse) qtl MP:0002833 increased heart weight IAGP N RGD:5509061 20111116 MGI PMID:12118100 1301562 Hwq1_m heart weight quantitative locus 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12118100 1301562 Hwq1_m heart weight quantitative locus 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118100 1301563 Alcp3_m alcohol preference locus 3 (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:9880657 1301563 Alcp3_m alcohol preference locus 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9880657 1301564 Pltpq3_m phospholipid transfer protein activity QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592843 1301564 Pltpq3_m phospholipid transfer protein activity QTL 3 (mouse) qtl MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20111116 MGI PMID:14592843 1301565 Mnotch_m modifier of Notch (mouse) qtl MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20111116 MGI PMID:12388777 1301565 Mnotch_m modifier of Notch (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12388777 1301566 Adip3_m adiposity 3 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11178736 1301566 Adip3_m adiposity 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301569 Axtofd3_m anxiety-open field defecation 3 (mouse) qtl MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:14990867 1301569 Axtofd3_m anxiety-open field defecation 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11454769|PMID:14990867 1301569 Axtofd3_m anxiety-open field defecation 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160422 MGI Created by mouse qtl pipeline PMID:11454769 1301571 Arrd1_m age-related retinal degeneration 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12766041 1301571 Arrd1_m age-related retinal degeneration 1 (mouse) qtl MP:0031605 decreased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:12766041 1301572 Sluc30_m susceptibility to lung cancer 30 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1301572 Sluc30_m susceptibility to lung cancer 30 (mouse) qtl MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301574 Lmblgq5_m limb length QTL 5 (mouse) qtl MP:0004348 long femur IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301574 Lmblgq5_m limb length QTL 5 (mouse) qtl MP:0004357 long tibia IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301574 Lmblgq5_m limb length QTL 5 (mouse) qtl MP:0004370 long ulna IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301574 Lmblgq5_m limb length QTL 5 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301574 Lmblgq5_m limb length QTL 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301575 Tanidd3_m tally ho associated non-insulin dependednt diabetes mellitus 3 (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:11414755 1301575 Tanidd3_m tally ho associated non-insulin dependednt diabetes mellitus 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11414755 1301576 Wt6q2_m body weight (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:10353911 1301576 Wt6q2_m body weight (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1301578 Feml3_m femur length in high growth mice 3 (mouse) qtl MP:0001258 decreased body length IAGP N RGD:5509061 20111116 MGI PMID:16670015 1301578 Feml3_m femur length in high growth mice 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16670015 1301578 Feml3_m femur length in high growth mice 3 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16670015 1301578 Feml3_m femur length in high growth mice 3 (mouse) qtl MP:0003109 short femur IAGP N RGD:5509061 20111116 MGI PMID:16670015 1301578 Feml3_m femur length in high growth mice 3 (mouse) qtl MP:0004348 long femur IAGP N RGD:5509061 20111116 MGI PMID:11309659 1301578 Feml3_m femur length in high growth mice 3 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301578 Feml3_m femur length in high growth mice 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301578 Feml3_m femur length in high growth mice 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301580 Hrq2_m heart rate quantitative locus 2 (mouse) qtl MP:0002626 increased heart rate IAGP N RGD:5509061 20111116 MGI PMID:12118100 1301580 Hrq2_m heart rate quantitative locus 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118100 1301581 Char2_m P. chabaudi malaria resistance QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9398835|PMID:15170228|PMID:9398834 1301584 Lrdg2_m light induced retinal degeneration 2 (mouse) qtl MP:0001326 retina degeneration IAGP N RGD:5509061 20111116 MGI PMID:15112105 1301584 Lrdg2_m light induced retinal degeneration 2 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15112105 1301585 Cd4ts1_m CD4 T cell subset 1 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12595899 1301585 Cd4ts1_m CD4 T cell subset 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301585 Cd4ts1_m CD4 T cell subset 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301586 Stheal3_m soft tissue heal 3 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:11731492 1301586 Stheal3_m soft tissue heal 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11731492 1301587 Rrodp2_m rotarod performance 2 (mouse) qtl MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20111116 MGI PMID:14694905 1301587 Rrodp2_m rotarod performance 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14694905 1301588 Hrec_m hemotopoietic response to early cytokines (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:12010793 1301588 Hrec_m hemotopoietic response to early cytokines (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12010793 1301589 Obq14_m obesity QTL 14 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11210195 1301589 Obq14_m obesity QTL 14 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11210195 1301590 Pbwg3_m postnatal body weight growth 3 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 1301590 Pbwg3_m postnatal body weight growth 3 (mouse) qtl MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20111116 MGI PMID:15056934 1301590 Pbwg3_m postnatal body weight growth 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15056934 1301591 Chol7_m cholesterol 7 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14701919 1301591 Chol7_m cholesterol 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14701919 1301593 Heal8_m wound healing/regeneration 8 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:9751744 1301593 Heal8_m wound healing/regeneration 8 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12682777|PMID:9751744 1301593 Heal8_m wound healing/regeneration 8 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:9751744 1301594 Aod1b_m autoimmune ovarian dysgenesis 1b (mouse) qtl MP:0001868 ovary inflammation IAGP N RGD:5509061 20111116 MGI PMID:12794114 1301594 Aod1b_m autoimmune ovarian dysgenesis 1b (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12794114 1301594 Aod1b_m autoimmune ovarian dysgenesis 1b (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12794114 1301594 Aod1b_m autoimmune ovarian dysgenesis 1b (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12794114 1301595 Wt3q1_m body weight (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:10353911 1301595 Wt3q1_m body weight (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1301597 Anxty_m anxiety (mouse) qtl MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:12719372 1301597 Anxty_m anxiety (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12719372 1301598 Renf2_m renal failure 2 (mouse) qtl MP:0003606 kidney failure IAGP N RGD:5509061 20111116 MGI PMID:11839593 1301598 Renf2_m renal failure 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11839593 1301600 Hdlq29_m HDL QTL 29 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14993241 1301600 Hdlq29_m HDL QTL 29 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14993241 1301602 Bslm4_m basal locomotor activity 4 (mouse) qtl MP:0001399 hyperactivity IAGP N RGD:5509061 20111116 MGI PMID:14722723 1301602 Bslm4_m basal locomotor activity 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14722723 1301603 Hdl6_m HDL level 6 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12925895 1301603 Hdl6_m HDL level 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12925895 1301604 Eae1_m susceptibility to experimental allergic encephalomyelitis 1 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:2579140 1301604 Eae1_m susceptibility to experimental allergic encephalomyelitis 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:2579140 1301606 Hdlq6_m HDL QTL 6 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12805272 1301606 Hdlq6_m HDL QTL 6 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12805272 1301606 Hdlq6_m HDL QTL 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12805272 1301608 Emo3_m emotionality 3 (mouse) qtl MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20111116 MGI PMID:10080185 1301608 Emo3_m emotionality 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10080185 1301612 Skmw4_m skeletal muscle weight 4 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:14679300 1301612 Skmw4_m skeletal muscle weight 4 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14679300 1301614 Cgnz1_m chronic glomerulonephritis in NZM 1 (mouse) qtl MP:0001859 kidney inflammation IAGP N RGD:5509061 20111116 MGI PMID:11513551 1301614 Cgnz1_m chronic glomerulonephritis in NZM 1 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:11513551 1301614 Cgnz1_m chronic glomerulonephritis in NZM 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11513551 1301614 Cgnz1_m chronic glomerulonephritis in NZM 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11513551 1301615 Cfld3_m cystic fibrosis lung disease 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:12461645 1301615 Cfld3_m cystic fibrosis lung disease 3 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12461645 1301615 Cfld3_m cystic fibrosis lung disease 3 (mouse) qtl MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20111116 MGI PMID:12461645 1301616 Yaa2_m Y-linked autoimmune acceleration 2 (mouse) qtl MP:0001859 kidney inflammation IAGP N RGD:5509061 20111116 MGI PMID:9743333 1301616 Yaa2_m Y-linked autoimmune acceleration 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9743333 1301616 Yaa2_m Y-linked autoimmune acceleration 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9743333 1301618 Bglu1_m blood glucose level 1 (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:10894496 1301618 Bglu1_m blood glucose level 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10894496 1301620 Insq8_m insulin QTL 8 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:10871196 1301620 Insq8_m insulin QTL 8 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10871196 1301622 Eae12_m susceptibility to experimental allergic encephalomyelitis 12 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:10072563 1301622 Eae12_m susceptibility to experimental allergic encephalomyelitis 12 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10072563 1301623 Hipp1_m hippocampal weight 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11331379 1301623 Hipp1_m hippocampal weight 1 (mouse) qtl MP:0008282 enlarged hippocampus IAGP N RGD:5509061 20111116 MGI PMID:11331379 1301624 Aevm2_m autoimmune extremity vasculitis in MRL mice 2 (mouse) qtl MP:0001864 vascular inflammation IAGP N RGD:5509061 20111116 MGI PMID:12746919 1301624 Aevm2_m autoimmune extremity vasculitis in MRL mice 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12746919 1301624 Aevm2_m autoimmune extremity vasculitis in MRL mice 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12746919 1301626 Ltsd7_m lung tumor shape-determining 7 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517788 1301626 Ltsd7_m lung tumor shape-determining 7 (mouse) qtl MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20111116 MGI PMID:12517788 1301629 Obq7_m obesity QTL 7 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11210195 1301629 Obq7_m obesity QTL 7 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11210195 1301631 Orgwq7_m organ weight QTL 7 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301631 Orgwq7_m organ weight QTL 7 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301631 Orgwq7_m organ weight QTL 7 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301631 Orgwq7_m organ weight QTL 7 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301631 Orgwq7_m organ weight QTL 7 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301631 Orgwq7_m organ weight QTL 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12118102 1301631 Orgwq7_m organ weight QTL 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301631 Orgwq7_m organ weight QTL 7 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301632 Bw8q1_m body weight at 8 weeks QTL 1 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:12855751 1301632 Bw8q1_m body weight at 8 weeks QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12855751 1301632 Bw8q1_m body weight at 8 weeks QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12855751 1301632 Bw8q1_m body weight at 8 weeks QTL 1 (mouse) qtl MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:12855751 1301634 Eae6a_m susceptibility to experimental allergic encephalomyelitis 6a (mouse) qtl MP:0001847 brain inflammation IAGP N RGD:5509061 20111116 MGI PMID:9712054 1301634 Eae6a_m susceptibility to experimental allergic encephalomyelitis 6a (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9712054 1301634 Eae6a_m susceptibility to experimental allergic encephalomyelitis 6a (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:10438970 1301634 Eae6a_m susceptibility to experimental allergic encephalomyelitis 6a (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9712054 1301636 Lith5_m lithogenic gene 5 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:11842132 1301636 Lith5_m lithogenic gene 5 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11842132 1301639 Stnn_m striatal neuron number (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11319941 1301639 Stnn_m striatal neuron number (mouse) qtl MP:0008947 increased neuron number IAGP N RGD:5509061 20111116 MGI PMID:11319941 1301640 Lore4_m loss of righting induced by ethanol 4 (mouse) qtl MP:0001523 impaired righting response IAGP N RGD:5509061 20111116 MGI PMID:11964553 1301640 Lore4_m loss of righting induced by ethanol 4 (mouse) qtl MP:0002863 improved righting response IAGP N RGD:5509061 20111116 MGI PMID:11964553 1301640 Lore4_m loss of righting induced by ethanol 4 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11964553 1301640 Lore4_m loss of righting induced by ethanol 4 (mouse) qtl MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20111116 MGI PMID:15365296 1301640 Lore4_m loss of righting induced by ethanol 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11964553 1301641 Sbmd2_m spinal bone mineral density 2 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:10780854 1301641 Sbmd2_m spinal bone mineral density 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10780854 1301642 Hdlq20_m HDL QTL 20 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14993241 1301642 Hdlq20_m HDL QTL 20 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14993241 1301643 Melm3_m melanoma modifier 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11092979 1301643 Melm3_m melanoma modifier 3 (mouse) qtl MP:0009828 increased tumor latency IAGP N RGD:5509061 20111116 MGI PMID:11092979 1301643 Melm3_m melanoma modifier 3 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:11092979 1301643 Melm3_m melanoma modifier 3 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11092979 1301644 Lrnx7_m learning-contextual 7 (mouse) qtl MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20111116 MGI PMID:11105392 1301644 Lrnx7_m learning-contextual 7 (mouse) qtl MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20111116 MGI PMID:9354800 1301644 Lrnx7_m learning-contextual 7 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11105392 1301645 Loca1_m locomotor activity 1 (mouse) qtl MP:0002574 increased vertical activity IAGP N RGD:5509061 20111116 MGI PMID:14694905 1301645 Loca1_m locomotor activity 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14694905 1301645 Loca1_m locomotor activity 1 (mouse) qtl MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:14694905 1301647 Elpt_m elevated leptin (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:12765967 1301647 Elpt_m elevated leptin (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12765967 1301647 Elpt_m elevated leptin (mouse) qtl MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20201001 MGI PMID:12765967 1301649 Psl1_m promotion susceptibility QTL 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9364205 1301649 Psl1_m promotion susceptibility QTL 1 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:9364205 1301649 Psl1_m promotion susceptibility QTL 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9364205 1301650 Asbb1_m autoimmune susceptibility in C57BL/6J and BALB/c 1 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:11994421 1301650 Asbb1_m autoimmune susceptibility in C57BL/6J and BALB/c 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11994421 1301651 Tlf2_m T lymphocyte fraction 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9754812 1301651 Tlf2_m T lymphocyte fraction 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9754812 1301651 Tlf2_m T lymphocyte fraction 2 (mouse) qtl MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20111116 MGI PMID:9754812 1301652 Cpfd2_m cerebellum pattern fissures (mouse) qtl MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20111116 MGI PMID:11529272 1301652 Cpfd2_m cerebellum pattern fissures (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11529272 1301653 Obq15_m obesity QTL 15 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11210195 1301653 Obq15_m obesity QTL 15 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11210195 1301655 Bmd12_m bone mineral density 12 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11450694 1301655 Bmd12_m bone mineral density 12 (mouse) qtl MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:11450694 1301656 Hpnr5_m Heligmosomoides polygyrus nematode resistance 5 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:14507332 1301657 Afw2_m abdominal fat weight QTL 2 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141016 MGI PMID:9725853 1301657 Afw2_m abdominal fat weight QTL 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089|PMID:9725853 1301657 Afw2_m abdominal fat weight QTL 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20141017 MGI Created by mouse qtl pipeline PMID:9725853 1301658 Radpf3_m radiation pulmonary fibrosis 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:12097289 1301658 Radpf3_m radiation pulmonary fibrosis 3 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12097289 1301658 Radpf3_m radiation pulmonary fibrosis 3 (mouse) qtl MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20111116 MGI PMID:12097289 1301659 Arrd2_m age-related retinal degeneration 2 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20170811 MGI Created by mouse qtl pipeline PMID:12766041 1301659 Arrd2_m age-related retinal degeneration 2 (mouse) qtl MP:0031605 decreased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:12766041 1301660 Iba1_m induction of brown adipocytes 1 (mouse) qtl MP:0003012 obsolete no phenotypic analysis IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10931824 1301663 Skull9_m skull morphology 9 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301663 Skull9_m skull morphology 9 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301663 Skull9_m skull morphology 9 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301664 Feml1_m femur length in high growth mice 1 (mouse) qtl MP:0004348 long femur IAGP N RGD:5509061 20111116 MGI PMID:11309659 1301664 Feml1_m femur length in high growth mice 1 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301664 Feml1_m femur length in high growth mice 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301666 Eae13_m susceptibility to experimental allergic encephalomyelitis 13 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:10072563 1301666 Eae13_m susceptibility to experimental allergic encephalomyelitis 13 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10072563 1301667 Lxw5_m lupus BXSB x NZW 5 (mouse) qtl MP:0000691 enlarged spleen IAGP N RGD:5509061 20111116 MGI PMID:14662843 1301667 Lxw5_m lupus BXSB x NZW 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:14662843 1301667 Lxw5_m lupus BXSB x NZW 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14662843 1301667 Lxw5_m lupus BXSB x NZW 5 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14662843 1301668 nctm2_m Nakano cataract modifier 2 (mouse) qtl MP:0001304 cataract IAGP N RGD:5509061 20111116 MGI PMID:12470976 1301668 nctm2_m Nakano cataract modifier 2 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12470976 1301669 Hdlq28_m HDL QTL 28 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14993241 1301669 Hdlq28_m HDL QTL 28 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14993241 1301671 Lorp1_m loss of righting due to propofol 1 (mouse) qtl MP:0002863 improved righting response IAGP N RGD:5509061 20111116 MGI PMID:9477059 1301671 Lorp1_m loss of righting due to propofol 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9477059 1301671 Lorp1_m loss of righting due to propofol 1 (mouse) qtl MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20111116 MGI PMID:9477059 1301672 Lipq1_m lipoprotein QTL 1 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14722362 1301672 Lipq1_m lipoprotein QTL 1 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14722362 1301672 Lipq1_m lipoprotein QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14722362 1301673 Gvhd5_m graft-versus host disease 5 (mouse) qtl MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:11100271 1301673 Gvhd5_m graft-versus host disease 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11100271 1301674 Asthm2_m asthma 2 (mouse) qtl MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20111116 MGI PMID:10072427 1301674 Asthm2_m asthma 2 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10072427 1301676 Nidd6_m non-insulin-dependent diabetes mellitus 6 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:10331427 1301676 Nidd6_m non-insulin-dependent diabetes mellitus 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10331427 1301678 Abpr_m aberrant B cell proliferation (mouse) qtl MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:14695357 1301680 Vpantd_m VPA induced neural tube defect (mouse) qtl MP:0000914 exencephaly IAGP N RGD:5509061 20111116 MGI PMID:15170225 1301680 Vpantd_m VPA induced neural tube defect (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15170225 1301680 Vpantd_m VPA induced neural tube defect (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20150302 MGI Created by mouse qtl pipeline PMID:15170225 1301680 Vpantd_m VPA induced neural tube defect (mouse) qtl MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20150305 MGI PMID:15170225 1301682 Bglq5_m body growth late QTL 5 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:8846907 1301682 Bglq5_m body growth late QTL 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10689807 1301685 Estq2_m estradiol regulated response QTL 2 (mouse) qtl MP:0004904 increased uterus weight IAGP N RGD:5509061 20111116 MGI PMID:9927277 1301685 Estq2_m estradiol regulated response QTL 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9927277 1301686 Trmq1_m T cell ratio modifier QTL 1 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12070778 1301686 Trmq1_m T cell ratio modifier QTL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12070778 1301686 Trmq1_m T cell ratio modifier QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12070778 1301687 Mnic2_m macronutrient intake (mouse) qtl MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20111116 MGI PMID:12388789 1301687 Mnic2_m macronutrient intake (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12388789 1301689 Skull18_m skull morphology 18 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301689 Skull18_m skull morphology 18 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301689 Skull18_m skull morphology 18 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301690 Hdlq9_m HDL QTL 9 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12805272 1301690 Hdlq9_m HDL QTL 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12805272 1301691 Cdcs10_m cytokine deficiency colitis susceptibility 10 (mouse) qtl MP:0001858 intestinal inflammation IAGP N RGD:5509061 20111116 MGI PMID:11707574 1301691 Cdcs10_m cytokine deficiency colitis susceptibility 10 (mouse) qtl MP:0001858 intestinal inflammation IAGP N RGD:5509061 20111116 MGI PMID:12213197 1301691 Cdcs10_m cytokine deficiency colitis susceptibility 10 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12213197 1301691 Cdcs10_m cytokine deficiency colitis susceptibility 10 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12213197 1301693 Sle6_m systemic lupus erythematosus susceptibility 6 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:10485648 1301693 Sle6_m systemic lupus erythematosus susceptibility 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10485648 1301694 Rear2_m rearing 2 (mouse) qtl MP:0002574 increased vertical activity IAGP N RGD:5509061 20111116 MGI PMID:14694905 1301694 Rear2_m rearing 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14694905 1301696 Wt6q3_m body weight (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:10353911 1301696 Wt6q3_m body weight (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1301697 Sluc18_m susceptibility to lung cancer 18 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1301697 Sluc18_m susceptibility to lung cancer 18 (mouse) qtl MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301697 Sluc18_m susceptibility to lung cancer 18 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:11584065 1301699 Pbwg6_m postnatal body weight growth 6 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:11003694 1301699 Pbwg6_m postnatal body weight growth 6 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 1301699 Pbwg6_m postnatal body weight growth 6 (mouse) qtl MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20111116 MGI PMID:15056934 1301699 Pbwg6_m postnatal body weight growth 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11003694 1301700 Pctr2_m plasmacytoma resistance 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8313388 1301700 Pctr2_m plasmacytoma resistance 2 (mouse) qtl MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:8313388 1301701 Aggr1_m aggression 1 (mouse) qtl MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20111116 MGI PMID:11826145 1301701 Aggr1_m aggression 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11826145 1301703 Bomd3_m bone mineral density 3 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:11697791 1301703 Bomd3_m bone mineral density 3 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:11697792 1301703 Bomd3_m bone mineral density 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11697792 1301704 Dbsty1_m diabesity 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11042154 1301704 Dbsty1_m diabesity 1 (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:11042154 1301704 Dbsty1_m diabesity 1 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:11042154 1301704 Dbsty1_m diabesity 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11042154 1301704 Dbsty1_m diabesity 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11042154 1301705 Sles3_m systemic lupus erythmatosus suppressor 3 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:10485648 1301705 Sles3_m systemic lupus erythmatosus suppressor 3 (mouse) qtl MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:10485648 1301705 Sles3_m systemic lupus erythmatosus suppressor 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10485648 1301706 Cdcs6_m cytokine deficiency colitis susceptibility 6 (mouse) qtl MP:0001858 intestinal inflammation IAGP N RGD:5509061 20111116 MGI PMID:11707574 1301706 Cdcs6_m cytokine deficiency colitis susceptibility 6 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11707574 1301706 Cdcs6_m cytokine deficiency colitis susceptibility 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11707574 1301707 Mwq3_m molecular weight of quadriceps QTL 3 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:11116089 1301707 Mwq3_m molecular weight of quadriceps QTL 3 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089 1301710 Bmd5_m bone mineral density 5 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:12568393 1301710 Bmd5_m bone mineral density 5 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:14667144 1301710 Bmd5_m bone mineral density 5 (mouse) qtl MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20111116 MGI PMID:17371164 1301710 Bmd5_m bone mineral density 5 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11450694|PMID:12568393 1301710 Bmd5_m bone mineral density 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11450694|PMID:12568393 1301710 Bmd5_m bone mineral density 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11450694|PMID:12568393 1301710 Bmd5_m bone mineral density 5 (mouse) qtl MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20111215 MGI PMID:12568393 1301710 Bmd5_m bone mineral density 5 (mouse) qtl MP:0010968 decreased compact bone area IAGP N RGD:5509061 20220922 MGI PMID:14667144 1301710 Bmd5_m bone mineral density 5 (mouse) qtl MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:11450694 1301710 Bmd5_m bone mineral density 5 (mouse) qtl MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:12568393 1301710 Bmd5_m bone mineral density 5 (mouse) qtl MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20220922 MGI PMID:11450694 1301710 Bmd5_m bone mineral density 5 (mouse) qtl MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20220922 MGI PMID:12568393 1301711 Tbrs3_m tuberculosis resistance 3 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:11197687 1301711 Tbrs3_m tuberculosis resistance 3 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:12740444 1301711 Tbrs3_m tuberculosis resistance 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11197687 1301712 Idd9.1_m insulin dependent diabetes susceptibility 9.1 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:10933399 1301712 Idd9.1_m insulin dependent diabetes susceptibility 9.1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10933399 1301712 Idd9.1_m insulin dependent diabetes susceptibility 9.1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10933399 1301712 Idd9.1_m insulin dependent diabetes susceptibility 9.1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10933399 1301712 Idd9.1_m insulin dependent diabetes susceptibility 9.1 (mouse) qtl MP:0008039 increased NK T cell number IAGP N RGD:5509061 20111116 MGI PMID:12759418 1301713 Dbsty2_m diabesity 2 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11042154 1301713 Dbsty2_m diabesity 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11042154 1301714 Vertcling_m vertical clinging (mouse) qtl MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20111116 MGI PMID:10086232 1301714 Vertcling_m vertical clinging (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10086232 1301715 Elmaz2_m elevated maze behavior 2 (mouse) qtl MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20111116 MGI PMID:11420611 1301715 Elmaz2_m elevated maze behavior 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11420611 1301716 Aeyo_m age of eyelid opening (mouse) qtl MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20111116 MGI PMID:10086232 1301716 Aeyo_m age of eyelid opening (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10086232 1301717 Adip4_m adiposity 4 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11178736 1301717 Adip4_m adiposity 4 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:11178736 1301717 Adip4_m adiposity 4 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301717 Adip4_m adiposity 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301718 Pbw3_m pentobarbital withdrawal QTL 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11529278|PMID:16436183 1301718 Pbw3_m pentobarbital withdrawal QTL 3 (mouse) qtl MP:0009775 increased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:11529278 1301718 Pbw3_m pentobarbital withdrawal QTL 3 (mouse) qtl MP:0009775 increased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:16436183 1301720 Hpnr8_m Heligmosomoides polygyrus nematode resistance 8 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:14507332 1301721 Lipq3_m lipoprotein QTL 3 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14722362 1301721 Lipq3_m lipoprotein QTL 3 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14722362 1301721 Lipq3_m lipoprotein QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14722362 1301722 Cia9_m collagen induced arthritis QTL 9 (mouse) qtl MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20111116 MGI PMID:11433381 1301722 Cia9_m collagen induced arthritis QTL 9 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11433381 1301722 Cia9_m collagen induced arthritis QTL 9 (mouse) qtl MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11433381 1301722 Cia9_m collagen induced arthritis QTL 9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11433381 1301723 Fcsa7_m femoral cross-sectional area 7 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12369778 1301723 Fcsa7_m femoral cross-sectional area 7 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12369778 1301723 Fcsa7_m femoral cross-sectional area 7 (mouse) qtl MP:0008158 increased diameter of femur IAGP N RGD:5509061 20111116 MGI PMID:12369778 1301724 Pcd4ts1_m p-glycoprotein positive CD4 T cell subset 1 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12595899 1301724 Pcd4ts1_m p-glycoprotein positive CD4 T cell subset 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301724 Pcd4ts1_m p-glycoprotein positive CD4 T cell subset 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301725 Lifespan1_m life span 1 (mouse) qtl MP:0001661 extended life span IAGP N RGD:5509061 20111116 MGI PMID:11773201 1301725 Lifespan1_m life span 1 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11773201 1301726 Tlq1_m telomere length QTL 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9671732 1301726 Tlq1_m telomere length QTL 1 (mouse) qtl MP:0030927 decreased telomere length IAGP N RGD:5509061 20230824 MGI PMID:9671732 1301726 Tlq1_m telomere length QTL 1 (mouse) qtl MP:0030928 increased telomere length IAGP N RGD:5509061 20230824 MGI PMID:9671732 1301728 Ffal1_m free fatty acid level 1 (mouse) qtl MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20111116 MGI PMID:12925895 1301728 Ffal1_m free fatty acid level 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12925895 1301730 Szv3_m seizure severity 3 (mouse) qtl MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20111116 MGI PMID:11472065 1301730 Szv3_m seizure severity 3 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1301730 Szv3_m seizure severity 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1301733 Heal3_m wound healing/regeneration 3 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:9751744 1301733 Heal3_m wound healing/regeneration 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12682777|PMID:9751744 1301733 Heal3_m wound healing/regeneration 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:9751744 1301734 Acsns2_m Angiostrongylus costaricensis nematode susceptibility 2 (mouse) qtl MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:11862393 1301734 Acsns2_m Angiostrongylus costaricensis nematode susceptibility 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11862393 1301737 Insq9_m insulin QTL 9 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:10871196 1301737 Insq9_m insulin QTL 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10871196 1301738 Rhs1_m resistance to herpes simplex virus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11342599 1301738 Rhs1_m resistance to herpes simplex virus 1 (mouse) qtl MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:11342599 1301739 Pitm2_m prion incubation time 2 (mouse) qtl MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20111116 MGI PMID:11404459 1301739 Pitm2_m prion incubation time 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11404459 1301740 Bwq2_m body weight QTL 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15472465 1301740 Bwq2_m body weight QTL 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:18227763 1301740 Bwq2_m body weight QTL 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:9657845 1301740 Bwq2_m body weight QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9657845 1301740 Bwq2_m body weight QTL 2 (mouse) qtl MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20111116 MGI PMID:15472465 1301741 Lith2_m lithogenic gene 2 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:11074014 1301741 Lith2_m lithogenic gene 2 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11074014 1301742 Tnfp_m tumor necrosis factor protection (mouse) qtl MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20111116 MGI PMID:10049582 1301742 Tnfp_m tumor necrosis factor protection (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10049582 1301744 Hdlq11_m HDL QTL 11 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12588951 1301744 Hdlq11_m HDL QTL 11 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12588951 1301747 Eae21_m experimental allergic encephalomyelitis 21 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10934166 1301747 Eae21_m experimental allergic encephalomyelitis 21 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10934166 1301747 Eae21_m experimental allergic encephalomyelitis 21 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10934166 1301747 Eae21_m experimental allergic encephalomyelitis 21 (mouse) qtl MP:0021002 brain lesion IAGP N RGD:5509061 20210805 MGI PMID:10934166 1301748 Abbp1_m A/J and C57BL/6 blood pressure 1 (mouse) qtl MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20111116 MGI PMID:14612590 1301748 Abbp1_m A/J and C57BL/6 blood pressure 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14612590 1301749 Orgwq1_m organ weight QTL 1 (mouse) qtl MP:0002834 decreased heart weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301749 Orgwq1_m organ weight QTL 1 (mouse) qtl MP:0003918 decreased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301749 Orgwq1_m organ weight QTL 1 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301749 Orgwq1_m organ weight QTL 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301749 Orgwq1_m organ weight QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12118102 1301749 Orgwq1_m organ weight QTL 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301749 Orgwq1_m organ weight QTL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301749 Orgwq1_m organ weight QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301754 Cocia5_m cocaine induced activation 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12777963 1301754 Cocia5_m cocaine induced activation 5 (mouse) qtl MP:0008911 induced hyperactivity IAGP N RGD:5509061 20220421 MGI PMID:12777963 1301754 Cocia5_m cocaine induced activation 5 (mouse) qtl MP:0020871 abnormal locomotor response to cocaine IAGP N RGD:5509061 20220421 MGI PMID:12777963 1301755 Hrq1_m heart rate quantitative locus 1 (mouse) qtl MP:0002626 increased heart rate IAGP N RGD:5509061 20111116 MGI PMID:12118100 1301755 Hrq1_m heart rate quantitative locus 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118100 1301756 Pgia1_m proteoglycan induced arthritis 1 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:10615997 1301756 Pgia1_m proteoglycan induced arthritis 1 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20111116 MGI PMID:10615997 1301756 Pgia1_m proteoglycan induced arthritis 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10615997|PMID:15084914 1301756 Pgia1_m proteoglycan induced arthritis 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:10615997 1301758 Fcsa3_m femoral cross-sectional area 3 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12369778 1301758 Fcsa3_m femoral cross-sectional area 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12369778 1301758 Fcsa3_m femoral cross-sectional area 3 (mouse) qtl MP:0008158 increased diameter of femur IAGP N RGD:5509061 20111116 MGI PMID:12369778 1301759 Sles1_m systemic lupus erythmatosus suppressor 1 (mouse) qtl MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20111116 MGI PMID:10485648 1301759 Sles1_m systemic lupus erythmatosus suppressor 1 (mouse) qtl MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20111116 MGI PMID:16002707 1301759 Sles1_m systemic lupus erythmatosus suppressor 1 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:10485648 1301759 Sles1_m systemic lupus erythmatosus suppressor 1 (mouse) qtl MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:10485648 1301759 Sles1_m systemic lupus erythmatosus suppressor 1 (mouse) qtl MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:16002707 1301759 Sles1_m systemic lupus erythmatosus suppressor 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10485648 1301759 Sles1_m systemic lupus erythmatosus suppressor 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:10485648 1301762 Nidd2n_m non-insulin-dependent diabetes mellitus 2 in NSY (mouse) qtl MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20111116 MGI PMID:10331425 1301762 Nidd2n_m non-insulin-dependent diabetes mellitus 2 in NSY (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10331425 1301764 Chab4_m cholesterol absorption 4 (mouse) qtl MP:0002646 increased intestinal cholesterol absorption IAGP N RGD:5509061 20111116 MGI PMID:11714849 1301764 Chab4_m cholesterol absorption 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11714849 1301764 Chab4_m cholesterol absorption 4 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11714849 1301765 Skull15_m skull morphology 15 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301765 Skull15_m skull morphology 15 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301765 Skull15_m skull morphology 15 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301766 Desp1_m despair 1 (mouse) qtl MP:0002573 behavioral despair IAGP N RGD:5509061 20111116 MGI PMID:11875023 1301766 Desp1_m despair 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11875023 1301767 Fcsa2_m femoral cross-sectional area 2 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12369778 1301767 Fcsa2_m femoral cross-sectional area 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12369778 1301767 Fcsa2_m femoral cross-sectional area 2 (mouse) qtl MP:0008158 increased diameter of femur IAGP N RGD:5509061 20111116 MGI PMID:12369778 1301768 Bw14_m body weight QTL 14 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11116089 1301768 Bw14_m body weight QTL 14 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089 1301769 Orgwq2_m organ weight QTL 2 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301769 Orgwq2_m organ weight QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12118102 1301769 Orgwq2_m organ weight QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301769 Orgwq2_m organ weight QTL 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301771 Pcyts6_m plasmacytoma susceptibility 6 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12149518 1301771 Pcyts6_m plasmacytoma susceptibility 6 (mouse) qtl MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20111116 MGI PMID:12149518 1301772 Skull3_m skull morphology 3 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301772 Skull3_m skull morphology 3 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301772 Skull3_m skull morphology 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301773 Stheal7_m soft tissue heal 7 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:11731492 1301773 Stheal7_m soft tissue heal 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11731492 1301775 Hdis_m horizontal distance traveled (mouse) qtl MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20111116 MGI PMID:14694905 1301775 Hdis_m horizontal distance traveled (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14694905 1301779 Dpml_m dopamine loss (mouse) qtl MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20111116 MGI PMID:12967986 1301779 Dpml_m dopamine loss (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12967986 1301779 Dpml_m dopamine loss (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12967986 1301780 Tir3_m trypanosome infection response 3 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:15859356 1301780 Tir3_m trypanosome infection response 3 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:18253157 1301780 Tir3_m trypanosome infection response 3 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:9171834 1301780 Tir3_m trypanosome infection response 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9171834 1301781 Capsq3_m capsaicin sensitivity related QTL 3 (mouse) qtl MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20111116 MGI PMID:14499433 1301781 Capsq3_m capsaicin sensitivity related QTL 3 (mouse) qtl MP:0005394 taste/olfaction phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14499433 1301782 Chol11_m cholesterol 11 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14872007 1301782 Chol11_m cholesterol 11 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14872007 1301783 Bhr1_m bronchial hyperresponsiveness 1 (mouse) qtl MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20111116 MGI PMID:15657107 1301783 Bhr1_m bronchial hyperresponsiveness 1 (mouse) qtl MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20111116 MGI PMID:7550342 1301783 Bhr1_m bronchial hyperresponsiveness 1 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7550342 1301784 Ses2_m salmonella enteritidis susceptibility 2 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:12058254 1301784 Ses2_m salmonella enteritidis susceptibility 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058254 1301785 Lmblgq1_m limb length QTL 1 (mouse) qtl MP:0002764 short tibia IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301785 Lmblgq1_m limb length QTL 1 (mouse) qtl MP:0003109 short femur IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301785 Lmblgq1_m limb length QTL 1 (mouse) qtl MP:0004351 short humerus IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301785 Lmblgq1_m limb length QTL 1 (mouse) qtl MP:0004359 short ulna IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301785 Lmblgq1_m limb length QTL 1 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301785 Lmblgq1_m limb length QTL 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301786 Bpq3_m blood pressure QTL 3 (mouse) qtl MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20111116 MGI PMID:11161799 1301786 Bpq3_m blood pressure QTL 3 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11161799 1301787 Bsc1_m brain size control 1 (mouse) qtl MP:0002176 increased brain weight IAGP N RGD:5509061 20111116 MGI PMID:11319941 1301787 Bsc1_m brain size control 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11319941 1301787 Bsc1_m brain size control 1 (mouse) qtl MP:0005238 increased brain size IAGP N RGD:5509061 20111116 MGI PMID:11319941 1301788 Lbw8_m lupus NZB x NZW 8 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20111116 MGI PMID:7937857 1301788 Lbw8_m lupus NZB x NZW 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7937857 1301789 Pbwg4_m postnatal body weight growth 4 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 1301789 Pbwg4_m postnatal body weight growth 4 (mouse) qtl MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20111116 MGI PMID:15056934 1301789 Pbwg4_m postnatal body weight growth 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15056934 1301791 Char4_m P. chabaudi malaria resistance QTL 4 (mouse) qtl MP:0002640 reticulocytosis IAGP N RGD:5509061 20111116 MGI PMID:14595440 1301791 Char4_m P. chabaudi malaria resistance QTL 4 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:11535821 1301791 Char4_m P. chabaudi malaria resistance QTL 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11535821 1301791 Char4_m P. chabaudi malaria resistance QTL 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11535821 1301792 Hdlq10_m HDL QTL 10 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12588951 1301792 Hdlq10_m HDL QTL 10 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14701919 1301792 Hdlq10_m HDL QTL 10 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14701919|PMID:12588951|PMID:16685081 1301792 Hdlq10_m HDL QTL 10 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:12588951 1301795 Cbm3_m cerebellum weight 3 (mouse) qtl MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20111116 MGI PMID:11438585 1301795 Cbm3_m cerebellum weight 3 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11438585 1301796 Mop2_m morphine preference 2 (mouse) qtl MP:0002553 preference for addictive substance IAGP N RGD:5509061 20111116 MGI PMID:15508023 1301796 Mop2_m morphine preference 2 (mouse) qtl MP:0002553 preference for addictive substance IAGP N RGD:5509061 20111116 MGI PMID:8075641 1301796 Mop2_m morphine preference 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8075641 1301797 Idd1_m insulin dependent diabetes susceptibility 1 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:2576007 1301797 Idd1_m insulin dependent diabetes susceptibility 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8661724|PMID:2576007 1301797 Idd1_m insulin dependent diabetes susceptibility 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8661724|PMID:2576007 1301797 Idd1_m insulin dependent diabetes susceptibility 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8661724|PMID:2576007 1301797 Idd1_m insulin dependent diabetes susceptibility 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8661724|PMID:2576007 1301797 Idd1_m insulin dependent diabetes susceptibility 1 (mouse) qtl MP:0005580 periinsulitis IAGP N RGD:5509061 20111116 MGI PMID:8661724 1301797 Idd1_m insulin dependent diabetes susceptibility 1 (mouse) qtl MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20111116 MGI PMID:15309345 1301798 Hdlq31_m HDL QTL 31 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14993241 1301798 Hdlq31_m HDL QTL 31 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14993241 1301801 Cpfd5_m cerebellum pattern fissures (mouse) qtl MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20111116 MGI PMID:11529272 1301801 Cpfd5_m cerebellum pattern fissures (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11529272 1301802 Bglq8_m body growth late QTL 8 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:8846907 1301802 Bglq8_m body growth late QTL 8 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8846907 1301803 Stheal9_m soft tissue heal 9 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:11731492 1301803 Stheal9_m soft tissue heal 9 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:16341671 1301803 Stheal9_m soft tissue heal 9 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:18028142 1301803 Stheal9_m soft tissue heal 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16341671|PMID:11731492 1301803 Stheal9_m soft tissue heal 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:11731492 1301804 Bulb2_m bulb size 2 (mouse) qtl MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20111116 MGI PMID:11529276 1301804 Bulb2_m bulb size 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11529276 1301805 Mors2_m modifier of obesity related sterility 2 (mouse) qtl MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20111116 MGI PMID:9927300 1301805 Mors2_m modifier of obesity related sterility 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9927300 1301806 Actd2_m activity-distance traveled 2 (mouse) qtl MP:0001399 hyperactivity IAGP N RGD:5509061 20111116 MGI PMID:11105390 1301806 Actd2_m activity-distance traveled 2 (mouse) qtl MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20111116 MGI PMID:11105390 1301806 Actd2_m activity-distance traveled 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11105390 1301807 Alcp19_m alcohol preference locus 19 (mouse) qtl MP:0001425 abnormal alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:9880655 1301807 Alcp19_m alcohol preference locus 19 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9880655 1301808 Nhdlq1_m non-HDL QTL 1 (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14701919 1301808 Nhdlq1_m non-HDL QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15210844|PMID:14701919 1301808 Nhdlq1_m non-HDL QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20151113 MGI Created by mouse qtl pipeline PMID:14701919 1301809 Axtofd1_m anxiety-open field defecation 1 (mouse) qtl MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:14990867 1301809 Axtofd1_m anxiety-open field defecation 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11454769|PMID:14990867 1301809 Axtofd1_m anxiety-open field defecation 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160422 MGI Created by mouse qtl pipeline PMID:11454769 1301812 Hpnr3_m Heligmosomoides polygyrus nematode resistance 3 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:14507332 1301812 Hpnr3_m Heligmosomoides polygyrus nematode resistance 3 (mouse) qtl MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:12647241 1301812 Hpnr3_m Heligmosomoides polygyrus nematode resistance 3 (mouse) qtl MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:14507332 1301813 Skl3_m skeletal size (tail length) 3 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:11178736 1301813 Skl3_m skeletal size (tail length) 3 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301815 Sles2_m systemic lupus erythmatosus suppressor 2 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:10485648 1301815 Sles2_m systemic lupus erythmatosus suppressor 2 (mouse) qtl MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:10485648 1301815 Sles2_m systemic lupus erythmatosus suppressor 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10485648 1301816 Cocia7_m cocaine induced activation 7 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12777963 1301816 Cocia7_m cocaine induced activation 7 (mouse) qtl MP:0008911 induced hyperactivity IAGP N RGD:5509061 20220421 MGI PMID:12777963 1301816 Cocia7_m cocaine induced activation 7 (mouse) qtl MP:0020871 abnormal locomotor response to cocaine IAGP N RGD:5509061 20220421 MGI PMID:12777963 1301818 Ap1q_m alcohol preference 1 QTL (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:9726281 1301818 Ap1q_m alcohol preference 1 QTL (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9726281 1301820 Mop1_m morphine preference 1 (mouse) qtl MP:0002553 preference for addictive substance IAGP N RGD:5509061 20111116 MGI PMID:8075641 1301820 Mop1_m morphine preference 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8075641 1301821 Tapr_m T-cell and airway phenotype regulator (mouse) qtl MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11725301 1301821 Tapr_m T-cell and airway phenotype regulator (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11725301 1301822 Pgia2_m proteoglycan induced arthritis 2 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:10615997 1301822 Pgia2_m proteoglycan induced arthritis 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10615997 1301823 Bmd7_m bone mineral density 7 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:12490544 1301823 Bmd7_m bone mineral density 7 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:14667144 1301823 Bmd7_m bone mineral density 7 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20220923 MGI Created by mouse qtl pipeline PMID:11450694 1301823 Bmd7_m bone mineral density 7 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11450694 1301823 Bmd7_m bone mineral density 7 (mouse) qtl MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:11450694 1301823 Bmd7_m bone mineral density 7 (mouse) qtl MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:12568393 1301823 Bmd7_m bone mineral density 7 (mouse) qtl MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:12490544 1301823 Bmd7_m bone mineral density 7 (mouse) qtl MP:0021183 increased femoral compact bone area IAGP N RGD:5509061 20220922 MGI PMID:14667144 1301823 Bmd7_m bone mineral density 7 (mouse) qtl MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20220922 MGI PMID:11450694 1301823 Bmd7_m bone mineral density 7 (mouse) qtl MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20220922 MGI PMID:12568393 1301824 Susp_m suppressor of superoxide production (mouse) qtl MP:0005266 abnormal metabolism IAGP N RGD:5509061 20111116 MGI PMID:11937300 1301824 Susp_m suppressor of superoxide production (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11937300 1301825 Pbrgcsf1_m peripheral blood stem cell response to granulocyte colony stimulating factor 1 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:14725902 1301825 Pbrgcsf1_m peripheral blood stem cell response to granulocyte colony stimulating factor 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10688851 1301826 Pgia3_m proteoglycan induced arthritis 3 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10615997 1301826 Pgia3_m proteoglycan induced arthritis 3 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:10615997 1301826 Pgia3_m proteoglycan induced arthritis 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10615997 1301828 Insq5_m insulin QTL 5 (mouse) qtl MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:11109545 1301828 Insq5_m insulin QTL 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11109545 1301829 Thyls2_m thymic lymphoma susceptibility 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14514657 1301829 Thyls2_m thymic lymphoma susceptibility 2 (mouse) qtl MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20111215 MGI PMID:14514657 1301829 Thyls2_m thymic lymphoma susceptibility 2 (mouse) qtl MP:0004503 decreased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20111116 MGI PMID:14514657 1301829 Thyls2_m thymic lymphoma susceptibility 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:14514657 1301829 Thyls2_m thymic lymphoma susceptibility 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20241101 MGI Created by mouse qtl pipeline PMID:14514657 1301829 Thyls2_m thymic lymphoma susceptibility 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20241101 MGI Created by mouse qtl pipeline PMID:14514657 1301832 Bw17_m body weight QTL 17 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11109545 1301832 Bw17_m body weight QTL 17 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:11109545 1301832 Bw17_m body weight QTL 17 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11109545 1301834 Bits1_m bitterness sensitivity 1 (mouse) qtl MP:0004210 abnormal bitter taste sensitivity IAGP N RGD:5509061 20111116 MGI PMID:10609087 1301834 Bits1_m bitterness sensitivity 1 (mouse) qtl MP:0005394 taste/olfaction phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10609087 1301835 Carp3_m carcass protein in high growth mice 3 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:11309659 1301835 Carp3_m carcass protein in high growth mice 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301836 Heal5_m wound healing/regeneration 5 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:12682777 1301836 Heal5_m wound healing/regeneration 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12682777 1301837 Alcw2_m alcohol withdrawal 2 (mouse) qtl MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20111116 MGI PMID:18815268 1301837 Alcw2_m alcohol withdrawal 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9133412 1301837 Alcw2_m alcohol withdrawal 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9133412 1301837 Alcw2_m alcohol withdrawal 2 (mouse) qtl MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20111116 MGI PMID:18815268 1301837 Alcw2_m alcohol withdrawal 2 (mouse) qtl MP:0009775 increased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:12893462 1301837 Alcw2_m alcohol withdrawal 2 (mouse) qtl MP:0009775 increased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:14960011 1301837 Alcw2_m alcohol withdrawal 2 (mouse) qtl MP:0009776 decreased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:11978849 1301837 Alcw2_m alcohol withdrawal 2 (mouse) qtl MP:0009776 decreased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:14960011 1301837 Alcw2_m alcohol withdrawal 2 (mouse) qtl MP:0009776 decreased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:18815268 1301838 Sluc16_m susceptibility to lung cancer 16 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1301838 Sluc16_m susceptibility to lung cancer 16 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1301840 Ssial4_m susceptibility to sialadenitiss 4 (mouse) qtl MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20111116 MGI PMID:11937580 1301840 Ssial4_m susceptibility to sialadenitiss 4 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11937580 1301840 Ssial4_m susceptibility to sialadenitiss 4 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11937580 1301840 Ssial4_m susceptibility to sialadenitiss 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11937580 1301841 Lrnx9_m learning-contextual 9 (mouse) qtl MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20111116 MGI PMID:9354800 1301841 Lrnx9_m learning-contextual 9 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9354800 1301842 Gvhd4_m graft-versus host disease 4 (mouse) qtl MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20111116 MGI PMID:11100271 1301842 Gvhd4_m graft-versus host disease 4 (mouse) qtl MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:11100271 1301842 Gvhd4_m graft-versus host disease 4 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11100271 1301842 Gvhd4_m graft-versus host disease 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11100271 1301843 Listr1_m listeriosis resistance 1 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:11242105 1301843 Listr1_m listeriosis resistance 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11242105 1301845 Lxw4_m lupus BXSB x NZW 4 (mouse) qtl MP:0002082 postnatal lethality IAGP N RGD:5509061 20111116 MGI PMID:14662843 1301845 Lxw4_m lupus BXSB x NZW 4 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14662843 1301847 Fecq2_m fecundity QTL 2 (mouse) qtl MP:0001934 increased litter size IAGP N RGD:5509061 20111116 MGI PMID:9457667 1301847 Fecq2_m fecundity QTL 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9457667 1301849 Derm1_m dermititis 1 (mouse) qtl MP:0001194 dermatitis IAGP N RGD:5509061 20111116 MGI PMID:11261926 1301849 Derm1_m dermititis 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11261926 1301849 Derm1_m dermititis 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11261926 1301850 Fglu_m fasting glucose (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:9916873 1301850 Fglu_m fasting glucose (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9916873 1301851 Tria5_m T-cell receptor induced activation 5 (mouse) qtl MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20111116 MGI PMID:10384038 1301851 Tria5_m T-cell receptor induced activation 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10384038 1301851 Tria5_m T-cell receptor induced activation 5 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:10384038 1301852 Ltry_m laterality (mouse) qtl MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20111116 MGI PMID:12663540 1301852 Ltry_m laterality (mouse) qtl MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20111116 MGI PMID:12663540 1301852 Ltry_m laterality (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12663540 1301852 Ltry_m laterality (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12663540 1301853 Heal9_m wound healing/regeneration 9 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:12682777 1301853 Heal9_m wound healing/regeneration 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12682777 1301858 Smdq1_m segregation of mitochondrial DNA QTL 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12539044 1301858 Smdq1_m segregation of mitochondrial DNA QTL 1 (mouse) qtl MP:0006037 abnormal mitochondrial fission IAGP N RGD:5509061 20111116 MGI PMID:12539044 1301861 Scpro2_m stem cell proliferation 2 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:10094931 1301861 Scpro2_m stem cell proliferation 2 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:12200366 1301861 Scpro2_m stem cell proliferation 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10094931 1301861 Scpro2_m stem cell proliferation 2 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10094931 1301862 Tchol1_m total cholesterol level 1 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:11473059 1301862 Tchol1_m total cholesterol level 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11473059 1301863 Skull5_m skull morphology 5 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301863 Skull5_m skull morphology 5 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301863 Skull5_m skull morphology 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301864 Afw9_m abdominal fat weight QTL 9 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:11116089 1301864 Afw9_m abdominal fat weight QTL 9 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089 1301865 Hdlq19_m HDL QTL 19 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14592847 1301865 Hdlq19_m HDL QTL 19 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18048852 1301865 Hdlq19_m HDL QTL 19 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592847|PMID:18048852 1301865 Hdlq19_m HDL QTL 19 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:14592847 1301866 Cplaq3_m circadian period of locomotor activity 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14667146|PMID:8917949|PMID:10547923 1301867 Idd11_m insulin dependent diabetes susceptibility 11 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:8016086 1301867 Idd11_m insulin dependent diabetes susceptibility 11 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8016086|PMID:15814708 1301868 Fbgl1_m fasting blood glucose 1 (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:11473059 1301868 Fbgl1_m fasting blood glucose 1 (mouse) qtl MP:0002871 albuminuria IAGP N RGD:5509061 20111116 MGI PMID:15769825 1301868 Fbgl1_m fasting blood glucose 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11473059 1301868 Fbgl1_m fasting blood glucose 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11473059 1301871 Frp1_m free running period 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11381025 1301871 Frp1_m free running period 1 (mouse) qtl MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:11381025 1301872 Cd4ts3_m CD4 T cell subset 3 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12595899 1301872 Cd4ts3_m CD4 T cell subset 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301872 Cd4ts3_m CD4 T cell subset 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12595899 1301873 Hsl1_m hyperoxia susceptibility locus 1 (mouse) qtl MP:0002319 hyperoxia IAGP N RGD:5509061 20111116 MGI PMID:11751202 1301873 Hsl1_m hyperoxia susceptibility locus 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11751202 1301874 Hdlq16_m HDL QTL 16 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18772481 1301874 Hdlq16_m HDL QTL 16 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14592847 1301874 Hdlq16_m HDL QTL 16 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592847 1301875 Apmt1_m accelerator of polyoma-induced mammary tumors 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11003704 1301875 Apmt1_m accelerator of polyoma-induced mammary tumors 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:11003704 1301875 Apmt1_m accelerator of polyoma-induced mammary tumors 1 (mouse) qtl MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:11003704 1301875 Apmt1_m accelerator of polyoma-induced mammary tumors 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:11003704 1301876 Bits2_m bitterness sensitivity 2 (mouse) qtl MP:0004210 abnormal bitter taste sensitivity IAGP N RGD:5509061 20111116 MGI PMID:10609087 1301876 Bits2_m bitterness sensitivity 2 (mouse) qtl MP:0005394 taste/olfaction phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10609087 1301877 Bbaa3_m B.burgdorferi-associated arthritis 3 (mouse) qtl MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11704805 1301877 Bbaa3_m B.burgdorferi-associated arthritis 3 (mouse) qtl MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:9916719 1301877 Bbaa3_m B.burgdorferi-associated arthritis 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9916719 1301879 Insq10_m insulin QTL 10 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:10871196 1301879 Insq10_m insulin QTL 10 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10871196 1301880 Hypt_m hypertension (mouse) qtl MP:0000231 hypertension IAGP N RGD:5509061 20111116 MGI PMID:12697907 1301880 Hypt_m hypertension (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12697907 1301881 Trmq2_m T cell ratio modifier QTL 2 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:12070778 1301881 Trmq2_m T cell ratio modifier QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12070778 1301881 Trmq2_m T cell ratio modifier QTL 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12070778 1301882 Etohc2_m ethanol consumption 2 (mouse) qtl MP:0001425 abnormal alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:9880656 1301882 Etohc2_m ethanol consumption 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9880656 1301883 Skull12_m skull morphology 12 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301883 Skull12_m skull morphology 12 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301883 Skull12_m skull morphology 12 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301884 Musz3_m muscle size 3 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:12185459 1301884 Musz3_m muscle size 3 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12185459 1301886 Hdlq24_m HDL QTL 24 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14993241 1301886 Hdlq24_m HDL QTL 24 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14993241 1301887 Nidd4n_m non-insulin-dependent diabetes mellitus 4 in NSY (mouse) qtl MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20111116 MGI PMID:10331425 1301887 Nidd4n_m non-insulin-dependent diabetes mellitus 4 in NSY (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10331425 1301889 Tcsz3_m tooth central size 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:11973311 1301889 Tcsz3_m tooth central size 3 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11973311 1301889 Tcsz3_m tooth central size 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20171006 MGI Created by mouse qtl pipeline PMID:11973311 1301889 Tcsz3_m tooth central size 3 (mouse) qtl MP:0030091 macrodontia IAGP N RGD:5509061 20171005 MGI PMID:11973311 1301890 Adip7_m adiposity 7 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11178736 1301890 Adip7_m adiposity 7 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301891 Alcp25_m alcohol preference locus 25 (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:10443995 1301891 Alcp25_m alcohol preference locus 25 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10443995 1301892 Szs6_m seizure susceptibility 6 (mouse) qtl MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20111116 MGI PMID:10436030 1301892 Szs6_m seizure susceptibility 6 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10436030 1301892 Szs6_m seizure susceptibility 6 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10436030 1301894 Skull2_m skull morphology 2 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301894 Skull2_m skull morphology 2 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301894 Skull2_m skull morphology 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301895 Exq1_m exploratory and excitability QTL 1 (mouse) qtl MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20111116 MGI PMID:10234005 1301895 Exq1_m exploratory and excitability QTL 1 (mouse) qtl MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20111116 MGI PMID:10234005 1301895 Exq1_m exploratory and excitability QTL 1 (mouse) qtl MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20111116 MGI PMID:10234005 1301895 Exq1_m exploratory and excitability QTL 1 (mouse) qtl MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20111116 MGI PMID:10234005 1301895 Exq1_m exploratory and excitability QTL 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10234005|PMID:16104379 1301895 Exq1_m exploratory and excitability QTL 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20151016 MGI Created by mouse qtl pipeline PMID:10234005 1301895 Exq1_m exploratory and excitability QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10234005|PMID:16104379 1301895 Exq1_m exploratory and excitability QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20151016 MGI Created by mouse qtl pipeline PMID:10234005 1301897 Scc2_m colon tumor susceptibility 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8944029 1301897 Scc2_m colon tumor susceptibility 2 (mouse) qtl MP:0002020 increased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:8577718 1301897 Scc2_m colon tumor susceptibility 2 (mouse) qtl MP:0002020 increased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:8944029 1301901 Im5_m immunoregulatory 5 (mouse) qtl MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20111116 MGI PMID:8962125 1301901 Im5_m immunoregulatory 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8962125 1301902 Hrtfm4_m heart failure modifier 4 (mouse) qtl MP:0001661 extended life span IAGP N RGD:5509061 20111116 MGI PMID:14519689 1301902 Hrtfm4_m heart failure modifier 4 (mouse) qtl MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20111116 MGI PMID:14519689 1301902 Hrtfm4_m heart failure modifier 4 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14519689 1301902 Hrtfm4_m heart failure modifier 4 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14519689 1301902 Hrtfm4_m heart failure modifier 4 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14519689 1301903 Tlsm1_m thymic lymphoma susceptible 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7964490|PMID:9209340 1301903 Tlsm1_m thymic lymphoma susceptible 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20151113 MGI Created by mouse qtl pipeline PMID:9209340 1301903 Tlsm1_m thymic lymphoma susceptible 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20180406 MGI Created by mouse qtl pipeline PMID:7964490 1301903 Tlsm1_m thymic lymphoma susceptible 1 (mouse) qtl MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20111215 MGI PMID:7964490 1301903 Tlsm1_m thymic lymphoma susceptible 1 (mouse) qtl MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20111215 MGI PMID:8641972 1301903 Tlsm1_m thymic lymphoma susceptible 1 (mouse) qtl MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20111215 MGI PMID:9209340 1301903 Tlsm1_m thymic lymphoma susceptible 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:7964490 1301903 Tlsm1_m thymic lymphoma susceptible 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20241101 MGI Created by mouse qtl pipeline PMID:7964490 1301903 Tlsm1_m thymic lymphoma susceptible 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20241101 MGI Created by mouse qtl pipeline PMID:7964490 1301904 Iba2_m induction of brown adipocytes 2 (mouse) qtl MP:0003012 obsolete no phenotypic analysis IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10931824 1301907 Rends_m renal disease susceptibility (mouse) qtl MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20111116 MGI PMID:11884477 1301907 Rends_m renal disease susceptibility (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11884477 1301908 Lrdm2_m lymphoproliferation (Fas) renal disease modifier 2 (mouse) qtl MP:0001859 kidney inflammation IAGP N RGD:5509061 20111116 MGI PMID:1460423 1301908 Lrdm2_m lymphoproliferation (Fas) renal disease modifier 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1460423 1301908 Lrdm2_m lymphoproliferation (Fas) renal disease modifier 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1460423 1301909 Smdq2_m segregation of mitochondrial DNA QTL 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12539044 1301909 Smdq2_m segregation of mitochondrial DNA QTL 2 (mouse) qtl MP:0006037 abnormal mitochondrial fission IAGP N RGD:5509061 20111116 MGI PMID:12539044 1301911 Lbm9_m lean body mass 9 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:12185457 1301911 Lbm9_m lean body mass 9 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12185457 1301912 Oriq5_m ovulation rate QTL 5 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10491617 1301913 Frp3_m free running period 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11381025 1301913 Frp3_m free running period 3 (mouse) qtl MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:11381025 1301914 Ksc1_m keratinocyte stem cell locus 1 (mouse) qtl MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20111116 MGI PMID:12663500 1301914 Ksc1_m keratinocyte stem cell locus 1 (mouse) qtl MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20111116 MGI PMID:14594209 1301914 Ksc1_m keratinocyte stem cell locus 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12663500 1301915 Chab3_m cholesterol absorption 3 (mouse) qtl MP:0002646 increased intestinal cholesterol absorption IAGP N RGD:5509061 20111116 MGI PMID:11714849 1301915 Chab3_m cholesterol absorption 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11714849 1301915 Chab3_m cholesterol absorption 3 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11714849 1301918 Skull22_m skull morphology 22 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301918 Skull22_m skull morphology 22 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301918 Skull22_m skull morphology 22 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301919 Mnek1b_m modifier of Nek1 (NIMA-related expressed kinase 1 (mouse) qtl MP:0000208 decreased hematocrit IAGP N RGD:5509061 20111116 MGI PMID:10366444 1301919 Mnek1b_m modifier of Nek1 (NIMA-related expressed kinase 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10366444 1301920 Hpnr7_m Heligmosomoides polygyrus nematode resistance 7 (mouse) qtl MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20111116 MGI PMID:14507332 1301920 Hpnr7_m Heligmosomoides polygyrus nematode resistance 7 (mouse) qtl MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20111116 MGI PMID:14507332 1301921 Stheal2_m soft tissue heal 2 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:11731492 1301921 Stheal2_m soft tissue heal 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11731492 1301923 Lith6_m lithogenic gene 6 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:12810825 1301923 Lith6_m lithogenic gene 6 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12837957|PMID:12810825 1301923 Lith6_m lithogenic gene 6 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20150717 MGI Created by mouse qtl pipeline PMID:12810825 1301923 Lith6_m lithogenic gene 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12837957|PMID:12810825 1301924 Bmd10_m bone mineral density 10 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11450694|PMID:11957111 1301924 Bmd10_m bone mineral density 10 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:11450694 1301924 Bmd10_m bone mineral density 10 (mouse) qtl MP:0021186 decreased bone mineral density of vertebrae IAGP N RGD:5509061 20220915 MGI PMID:11450694 1301925 Ath6_m atherosclerosis 6 (mouse) qtl MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20111116 MGI PMID:10393218 1301925 Ath6_m atherosclerosis 6 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10393218 1301926 Adip6_m adiposity 6 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:11178736 1301926 Adip6_m adiposity 6 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301926 Adip6_m adiposity 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301926 Adip6_m adiposity 6 (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:11178736 1301928 Ltsd3_m lung tumor shape-determining 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517788 1301928 Ltsd3_m lung tumor shape-determining 3 (mouse) qtl MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20111116 MGI PMID:12517788 1301930 Papg1_m pulmonary adenoma progression 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9331067 1301930 Papg1_m pulmonary adenoma progression 1 (mouse) qtl MP:0002020 increased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:9331067 1301931 Pas9_m pulmonary adenoma susceptibility 9 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9790761 1301931 Pas9_m pulmonary adenoma susceptibility 9 (mouse) qtl MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20111116 MGI PMID:9790761 1301931 Pas9_m pulmonary adenoma susceptibility 9 (mouse) qtl MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20111116 MGI PMID:9790761 1301931 Pas9_m pulmonary adenoma susceptibility 9 (mouse) qtl MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20111116 MGI PMID:9790761 1301931 Pas9_m pulmonary adenoma susceptibility 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9790761 1301931 Pas9_m pulmonary adenoma susceptibility 9 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9790761 1301933 Insq6_m insulin QTL 6 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:10871196 1301933 Insq6_m insulin QTL 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10871196 1301934 Adip2_m adiposity 2 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11178736 1301934 Adip2_m adiposity 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301935 Skull24_m skull morphology 24 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301935 Skull24_m skull morphology 24 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301935 Skull24_m skull morphology 24 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301936 Trigq2_m triglyceride QTL 2 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:14974682 1301936 Trigq2_m triglyceride QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14974682 1301937 Skull10_m skull morphology 10 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301937 Skull10_m skull morphology 10 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301937 Skull10_m skull morphology 10 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301940 Carp2_m carcass protein in high growth mice 2 (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20111116 MGI PMID:16670015 1301940 Carp2_m carcass protein in high growth mice 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16670015 1301940 Carp2_m carcass protein in high growth mice 2 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:11309659 1301940 Carp2_m carcass protein in high growth mice 2 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:16670015 1301940 Carp2_m carcass protein in high growth mice 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301940 Carp2_m carcass protein in high growth mice 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1301940 Carp2_m carcass protein in high growth mice 2 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:16670015 1301940 Carp2_m carcass protein in high growth mice 2 (mouse) qtl MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16670015 1301944 Lmblgq3_m limb length QTL 3 (mouse) qtl MP:0002764 short tibia IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301944 Lmblgq3_m limb length QTL 3 (mouse) qtl MP:0003109 short femur IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301944 Lmblgq3_m limb length QTL 3 (mouse) qtl MP:0004351 short humerus IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301944 Lmblgq3_m limb length QTL 3 (mouse) qtl MP:0004359 short ulna IAGP N RGD:5509061 20111116 MGI PMID:12118102 1301944 Lmblgq3_m limb length QTL 3 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301944 Lmblgq3_m limb length QTL 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1301945 Skl7_m skeletal size (tail length) 7 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:11178736 1301945 Skl7_m skeletal size (tail length) 7 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301948 Elsgp3_m elevated serum gp70 3 (mouse) qtl MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20111116 MGI PMID:10903778 1301948 Elsgp3_m elevated serum gp70 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10903778 1301949 Skull20_m skull morphology 20 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1301949 Skull20_m skull morphology 20 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301949 Skull20_m skull morphology 20 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1301950 Otx2m1_m orthodenticle homolog 2 (Drosophila) modifier 1 (mouse) qtl MP:0000087 absent mandible IAGP N RGD:5509061 20111116 MGI PMID:12183386 1301950 Otx2m1_m orthodenticle homolog 2 (Drosophila) modifier 1 (mouse) qtl MP:0000088 short mandible IAGP N RGD:5509061 20111116 MGI PMID:12183386 1301950 Otx2m1_m orthodenticle homolog 2 (Drosophila) modifier 1 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12183386 1301950 Otx2m1_m orthodenticle homolog 2 (Drosophila) modifier 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12183386 1301951 Eila3_m ethanol induced locomotor activity 3 (mouse) qtl MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20111116 MGI PMID:12931787 1301951 Eila3_m ethanol induced locomotor activity 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12931787 1301952 Im3_m immunoregulatory 3 (mouse) qtl MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20111116 MGI PMID:9472069 1301952 Im3_m immunoregulatory 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9472069 1301953 Tmevd9_m Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 9 (mouse) qtl MP:0000921 demyelination IAGP N RGD:5509061 20111116 MGI PMID:12663542 1301953 Tmevd9_m Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 9 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12663542 1301955 Amp1_m amplitude of circadian rhythm 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11381025 1301955 Amp1_m amplitude of circadian rhythm 1 (mouse) qtl MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:11381025 1301956 Orch3_m autoimmune orchitis resistance 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7777570 1301956 Orch3_m autoimmune orchitis resistance 3 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7777570 1301959 Afw5_m abdominal fat weight QTL 5 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:9725853 1301959 Afw5_m abdominal fat weight QTL 5 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089|PMID:9725853 1301959 Afw5_m abdominal fat weight QTL 5 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20141017 MGI Created by mouse qtl pipeline PMID:9725853|PMID:11116089 1301959 Afw5_m abdominal fat weight QTL 5 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20141031 MGI Created by mouse qtl pipeline PMID:9725853 1301961 Bts1_m bladder tumor susceptibility 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9879827 1301961 Bts1_m bladder tumor susceptibility 1 (mouse) qtl MP:0002020 increased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:9879827 1301961 Bts1_m bladder tumor susceptibility 1 (mouse) qtl MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20111116 MGI PMID:9879827 1301961 Bts1_m bladder tumor susceptibility 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9879827 1301962 Eila2_m ethanol induced locomotor activity 2 (mouse) qtl MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20111116 MGI PMID:12931787 1301962 Eila2_m ethanol induced locomotor activity 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12931787 1301964 Bw8q2_m body weight at 8 weeks QTL 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:12855751 1301964 Bw8q2_m body weight at 8 weeks QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12855751 1301966 Lifespan2_m life span 2 (mouse) qtl MP:0001661 extended life span IAGP N RGD:5509061 20111116 MGI PMID:11773201 1301966 Lifespan2_m life span 2 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11773201 1301967 Hlq4_m heat loss QTL 4 (mouse) qtl MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20111116 MGI PMID:10353911 1301967 Hlq4_m heat loss QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1301968 Estq4_m estradiol regulated response QTL 4 (mouse) qtl MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20111116 MGI PMID:9927277 1301968 Estq4_m estradiol regulated response QTL 4 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9927277 1301969 Lbw5_m lupus NZB x NZW 5 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:7937857 1301969 Lbw5_m lupus NZB x NZW 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9922399|PMID:7937857 1301969 Lbw5_m lupus NZB x NZW 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:7937857 1301970 Heal11_m wound healing/regeneration 11 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:12682777 1301970 Heal11_m wound healing/regeneration 11 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12682777 1301971 Cia5_m collagen induced arthritis QTL 5 (mouse) qtl MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:9808201 1301971 Cia5_m collagen induced arthritis QTL 5 (mouse) qtl MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20111116 MGI PMID:15611280 1301971 Cia5_m collagen induced arthritis QTL 5 (mouse) qtl MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:15611280 1301971 Cia5_m collagen induced arthritis QTL 5 (mouse) qtl MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:15716976 1301971 Cia5_m collagen induced arthritis QTL 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15611280|PMID:15084914|PMID:9808201 1301971 Cia5_m collagen induced arthritis QTL 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:15611280|PMID:9808201 1301971 Cia5_m collagen induced arthritis QTL 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15611280|PMID:15084914|PMID:9808201 1301971 Cia5_m collagen induced arthritis QTL 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:15611280|PMID:9808201 1301974 Chab7_m cholesterol absorption 7 (mouse) qtl MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20111116 MGI PMID:11714849 1301974 Chab7_m cholesterol absorption 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11714849 1301974 Chab7_m cholesterol absorption 7 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11714849 1301975 Mol1_m modifier of LPS-response 1 (mouse) qtl MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:10585765 1301975 Mol1_m modifier of LPS-response 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10585765 1301975 Mol1_m modifier of LPS-response 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10585765 1301975 Mol1_m modifier of LPS-response 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10585765 1301977 Szs8_m seizure susceptibility 8 (mouse) qtl MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20111116 MGI PMID:11472065 1301977 Szs8_m seizure susceptibility 8 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1301977 Szs8_m seizure susceptibility 8 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1301978 Tmevd6_m Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 6 (mouse) qtl MP:0000921 demyelination IAGP N RGD:5509061 20111116 MGI PMID:12663542 1301978 Tmevd6_m Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 6 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12663542 1301979 Melm1_m melanoma modifier 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11092979 1301979 Melm1_m melanoma modifier 1 (mouse) qtl MP:0009828 increased tumor latency IAGP N RGD:5509061 20111116 MGI PMID:11092979 1301979 Melm1_m melanoma modifier 1 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:11092979 1301979 Melm1_m melanoma modifier 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11092979 1301980 Fcsa5_m femoral cross-sectional area 5 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12369778 1301980 Fcsa5_m femoral cross-sectional area 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12369778 1301980 Fcsa5_m femoral cross-sectional area 5 (mouse) qtl MP:0008158 increased diameter of femur IAGP N RGD:5509061 20111116 MGI PMID:12369778 1301981 Aaq1_m alcohol acceptance QTL 1 (mouse) qtl MP:0001425 abnormal alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:9399693 1301981 Aaq1_m alcohol acceptance QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9399693 1301982 Pltiq1_m phospholipid transfer protein inducibility QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592843 1301982 Pltiq1_m phospholipid transfer protein inducibility QTL 1 (mouse) qtl MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20111116 MGI PMID:14592843 1301983 Berr2_m berghei resistance locus 2 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:12114535 1301983 Berr2_m berghei resistance locus 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12114535 1301984 Pbd2_m peak bone density 2 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:12140680 1301984 Pbd2_m peak bone density 2 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:17002585 1301984 Pbd2_m peak bone density 2 (mouse) qtl MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:12140680 1301984 Pbd2_m peak bone density 2 (mouse) qtl MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20111116 MGI PMID:9922384 1301984 Pbd2_m peak bone density 2 (mouse) qtl MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20111116 MGI PMID:9922384 1301984 Pbd2_m peak bone density 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11697793 1301986 Bpq4_m blood pressure QTL 4 (mouse) qtl MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20111116 MGI PMID:11161799 1301986 Bpq4_m blood pressure QTL 4 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11161799 1301988 Bmd11_m bone mineral density 11 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11450694 1301988 Bmd11_m bone mineral density 11 (mouse) qtl MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:11450694 1301988 Bmd11_m bone mineral density 11 (mouse) qtl MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20220922 MGI PMID:11450694 1301988 Bmd11_m bone mineral density 11 (mouse) qtl MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20220922 MGI PMID:12568393 1301989 Hdlq18_m HDL QTL 18 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18772481 1301989 Hdlq18_m HDL QTL 18 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14592847 1301989 Hdlq18_m HDL QTL 18 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14872007 1301989 Hdlq18_m HDL QTL 18 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592847|PMID:14872007 1301989 Hdlq18_m HDL QTL 18 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:14592847 1301990 Arvm1_m autoimmune renal vasculitis 1 (mouse) qtl MP:0001864 vascular inflammation IAGP N RGD:5509061 20111116 MGI PMID:10940892 1301990 Arvm1_m autoimmune renal vasculitis 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10940892 1301990 Arvm1_m autoimmune renal vasculitis 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10940892 1301991 Wta3_m weight adult 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11178736 1301991 Wta3_m weight adult 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1301993 Cocia4_m cocaine induced activation 4 (mouse) qtl MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20111116 MGI PMID:12777963 1301993 Cocia4_m cocaine induced activation 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12777963 1301994 Ksc2_m keratinocyte stem cell locus 2 (mouse) qtl MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20111116 MGI PMID:12663500 1301994 Ksc2_m keratinocyte stem cell locus 2 (mouse) qtl MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20111116 MGI PMID:14594209 1301994 Ksc2_m keratinocyte stem cell locus 2 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12663500 1301995 Lprm1_m lymphoproliferation modifier 1 (mouse) qtl MP:0001864 vascular inflammation IAGP N RGD:5509061 20111116 MGI PMID:9403730 1301995 Lprm1_m lymphoproliferation modifier 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9403730 1301995 Lprm1_m lymphoproliferation modifier 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9403730 1301997 Cia7_m collagen induced arthritis QTL 7 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10453039 1301997 Cia7_m collagen induced arthritis QTL 7 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17312155 1301997 Cia7_m collagen induced arthritis QTL 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10453039 1301997 Cia7_m collagen induced arthritis QTL 7 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10453039 1301998 Bts2_m bladder tumor susceptibility 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9879827 1301998 Bts2_m bladder tumor susceptibility 2 (mouse) qtl MP:0002020 increased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:9879827 1301998 Bts2_m bladder tumor susceptibility 2 (mouse) qtl MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20111116 MGI PMID:9879827 1301998 Bts2_m bladder tumor susceptibility 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9879827 1301999 Lmr15_m leishmaniasis resistance 15 (mouse) qtl MP:0000599 enlarged liver IAGP N RGD:5509061 20111116 MGI PMID:12654824 1301999 Lmr15_m leishmaniasis resistance 15 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12654824 1301999 Lmr15_m leishmaniasis resistance 15 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12654824 1301999 Lmr15_m leishmaniasis resistance 15 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12654824 1301999 Lmr15_m leishmaniasis resistance 15 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12654824 1301999 Lmr15_m leishmaniasis resistance 15 (mouse) qtl MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20111116 MGI PMID:16511555 1302000 Pgia25_m proteoglycan induced arthritis 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12594249|PMID:12794840 1302000 Pgia25_m proteoglycan induced arthritis 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12594249|PMID:12794840 1302001 Bdln5_m body length 5 (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20111116 MGI PMID:12856282 1302001 Bdln5_m body length 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12856282 1302003 Sluc17_m susceptibility to lung cancer 17 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1302003 Sluc17_m susceptibility to lung cancer 17 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1302004 Lfp2_m long free running period 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309657 1302004 Lfp2_m long free running period 2 (mouse) qtl MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:11309657 1302005 Loco2_m locomotor activity 2 (mouse) qtl MP:0001399 hyperactivity IAGP N RGD:5509061 20111116 MGI PMID:12226705 1302005 Loco2_m locomotor activity 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12226705 1302006 Szs2_m seizure susceptibility 2 (mouse) qtl MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20111116 MGI PMID:9069121 1302006 Szs2_m seizure susceptibility 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9069121 1302006 Szs2_m seizure susceptibility 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9069121 1302007 Bbaa14_m B.burgdorferi-associated arthritis 14 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11704805 1302007 Bbaa14_m B.burgdorferi-associated arthritis 14 (mouse) qtl MP:0002493 increased IgG level IAGP N RGD:5509061 20111116 MGI PMID:11704805 1302007 Bbaa14_m B.burgdorferi-associated arthritis 14 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11704805 1302007 Bbaa14_m B.burgdorferi-associated arthritis 14 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:11704805 1302008 Gasa4_m gastritis type A susceptibility locus 4 (mouse) qtl MP:0001873 stomach inflammation IAGP N RGD:5509061 20111116 MGI PMID:11862406 1302008 Gasa4_m gastritis type A susceptibility locus 4 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11862406 1302008 Gasa4_m gastritis type A susceptibility locus 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11862406 1302009 Sbmd1_m spinal bone mineral density 1 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:10780854 1302009 Sbmd1_m spinal bone mineral density 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10780854 1302010 Wta1_m weight adult 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11178736 1302010 Wta1_m weight adult 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1302014 Hdlq23_m HDL QTL 23 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14993241 1302014 Hdlq23_m HDL QTL 23 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14993241 1302015 C10bw2_m castaneus 10 week body weight 2 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:11003694 1302015 C10bw2_m castaneus 10 week body weight 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11003694 1302016 Ltsd1_m lung tumor shape-determining 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517788 1302016 Ltsd1_m lung tumor shape-determining 1 (mouse) qtl MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20111116 MGI PMID:12517788 1302018 Wt3q2_m body weight (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:10353911 1302018 Wt3q2_m body weight (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1302020 Bbaa20_m B.burgdorferi-associated arthritis 20 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11704805 1302020 Bbaa20_m B.burgdorferi-associated arthritis 20 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11704805 1302021 Nidd1n_m non-insulin-dependent diabetes mellitus 1 in NSY (mouse) qtl MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20111116 MGI PMID:10331425 1302021 Nidd1n_m non-insulin-dependent diabetes mellitus 1 in NSY (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10331425 1302023 Orch4_m autoimmune orchitis resistance 4 (mouse) qtl MP:0001875 testis inflammation IAGP N RGD:5509061 20111116 MGI PMID:7777570 1302023 Orch4_m autoimmune orchitis resistance 4 (mouse) qtl MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:7777570 1302023 Orch4_m autoimmune orchitis resistance 4 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20141219 MGI Created by mouse qtl pipeline PMID:7777570 1302023 Orch4_m autoimmune orchitis resistance 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7777570 1302023 Orch4_m autoimmune orchitis resistance 4 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7777570 1302024 Skull7_m skull morphology 7 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1302024 Skull7_m skull morphology 7 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1302024 Skull7_m skull morphology 7 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1302025 Pas1_m pulmonary adenoma susceptibility 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9659579|PMID:7813906|PMID:8499946|PMID:8666392 1302025 Pas1_m pulmonary adenoma susceptibility 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20151225 MGI Created by mouse qtl pipeline PMID:9659579|PMID:8499946|PMID:8666392 1302025 Pas1_m pulmonary adenoma susceptibility 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20160101 MGI Created by mouse qtl pipeline PMID:8499946 1302025 Pas1_m pulmonary adenoma susceptibility 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:9659579|PMID:7813906|PMID:8499946|PMID:8666392 1302025 Pas1_m pulmonary adenoma susceptibility 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20151225 MGI Created by mouse qtl pipeline PMID:9659579|PMID:8499946|PMID:8666392 1302025 Pas1_m pulmonary adenoma susceptibility 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:9659579|PMID:7813906|PMID:8499946|PMID:8666392 1302025 Pas1_m pulmonary adenoma susceptibility 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20151225 MGI Created by mouse qtl pipeline PMID:9659579|PMID:8499946|PMID:8666392 1302028 Asbb3_m autoimmune susceptibility in C57BL/6J and BALB/c 3 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:11994421 1302028 Asbb3_m autoimmune susceptibility in C57BL/6J and BALB/c 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11994421 1302029 Sst1_m susceptibility to tuberculosis 1 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:10890913 1302029 Sst1_m susceptibility to tuberculosis 1 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:15470055 1302029 Sst1_m susceptibility to tuberculosis 1 (mouse) qtl MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:10890913 1302029 Sst1_m susceptibility to tuberculosis 1 (mouse) qtl MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20221201 MGI PMID:34151776 1302029 Sst1_m susceptibility to tuberculosis 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10890913 1302029 Sst1_m susceptibility to tuberculosis 1 (mouse) qtl MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20221201 MGI PMID:34151776 1302029 Sst1_m susceptibility to tuberculosis 1 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20221202 MGI Created by mouse qtl pipeline PMID:10890913 1302031 Bulb1_m bulb size 1 (mouse) qtl MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20111116 MGI PMID:11529276 1302031 Bulb1_m bulb size 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11529276 1302033 Nsv1_m Neuroadapted Sindbis viral RNA level 1 (mouse) qtl MP:0002418 increased susceptibility to viral infection IAGP N RGD:5509061 20111116 MGI PMID:11507212 1302033 Nsv1_m Neuroadapted Sindbis viral RNA level 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11507212 1302035 Lmb4_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0000691 enlarged spleen IAGP N RGD:5509061 20111116 MGI PMID:9449705 1302035 Lmb4_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20111116 MGI PMID:17548658 1302035 Lmb4_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20111116 MGI PMID:9449705 1302035 Lmb4_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9449705 1302035 Lmb4_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9449705 1302035 Lmb4_m lupus in MRL and B6 F2 cross (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9449705 1302037 Nktcn1_m natural killer T cell numbers 1 (mouse) qtl MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20111116 MGI PMID:17237411 1302037 Nktcn1_m natural killer T cell numbers 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12960309 1302037 Nktcn1_m natural killer T cell numbers 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12960309 1302037 Nktcn1_m natural killer T cell numbers 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12960309 1302037 Nktcn1_m natural killer T cell numbers 1 (mouse) qtl MP:0008039 increased NK T cell number IAGP N RGD:5509061 20111116 MGI PMID:12960309 1302037 Nktcn1_m natural killer T cell numbers 1 (mouse) qtl MP:0008039 increased NK T cell number IAGP N RGD:5509061 20111116 MGI PMID:17237411 1302038 Radpf1_m radiation pulmonary fibrosis 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:9393751 1302038 Radpf1_m radiation pulmonary fibrosis 1 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9393751 1302038 Radpf1_m radiation pulmonary fibrosis 1 (mouse) qtl MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20111116 MGI PMID:12097289 1302038 Radpf1_m radiation pulmonary fibrosis 1 (mouse) qtl MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20111116 MGI PMID:9393751 1302039 Oriq4_m ovulation rate QTL 4 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1302041 Tcsz2_m tooth central size 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:11973311 1302041 Tcsz2_m tooth central size 2 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11973311 1302041 Tcsz2_m tooth central size 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20171006 MGI Created by mouse qtl pipeline PMID:11973311 1302041 Tcsz2_m tooth central size 2 (mouse) qtl MP:0030091 macrodontia IAGP N RGD:5509061 20171005 MGI PMID:11973311 1302042 Acsns3_m Angiostrongylus costaricensis nematode susceptibility 3 (mouse) qtl MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:11862393 1302042 Acsns3_m Angiostrongylus costaricensis nematode susceptibility 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11862393 1302044 Nss1_m NOD Sjogren's syndrome 1 (mouse) qtl MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20111116 MGI PMID:11782015 1302044 Nss1_m NOD Sjogren's syndrome 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11782015 1302044 Nss1_m NOD Sjogren's syndrome 1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11782015 1302044 Nss1_m NOD Sjogren's syndrome 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11782015 1302047 Fubi1_m failure of ureteric bud invasion 1 (mouse) qtl MP:0000527 abnormal kidney development IAGP N RGD:5509061 20111116 MGI PMID:11733383 1302047 Fubi1_m failure of ureteric bud invasion 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11733383 1302049 Heal1_m wound healing/regeneration 1 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:9751744 1302049 Heal1_m wound healing/regeneration 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12682777|PMID:9751744 1302049 Heal1_m wound healing/regeneration 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:9751744 1302050 Radpf4_m radiation pulmonary fibrosis 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:12097289 1302050 Radpf4_m radiation pulmonary fibrosis 4 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12097289 1302050 Radpf4_m radiation pulmonary fibrosis 4 (mouse) qtl MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20111116 MGI PMID:12097289 1302054 Gct4_m granulosa cell tumorigenesis 4 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14678975|PMID:9721880 1302054 Gct4_m granulosa cell tumorigenesis 4 (mouse) qtl MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:14678975 1302054 Gct4_m granulosa cell tumorigenesis 4 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:14678975|PMID:9721880 1302054 Gct4_m granulosa cell tumorigenesis 4 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:14678975|PMID:9721880 1302054 Gct4_m granulosa cell tumorigenesis 4 (mouse) qtl MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20131226 MGI PMID:9721880 1302054 Gct4_m granulosa cell tumorigenesis 4 (mouse) qtl MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20131227 MGI PMID:14678975 1302055 Mob6_m multigenic obesity 6 (mouse) qtl MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16873689 1302055 Mob6_m multigenic obesity 6 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16873689 1302055 Mob6_m multigenic obesity 6 (mouse) qtl MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:9616220 1302055 Mob6_m multigenic obesity 6 (mouse) qtl MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16873689 1302055 Mob6_m multigenic obesity 6 (mouse) qtl MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16873689 1302055 Mob6_m multigenic obesity 6 (mouse) qtl MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20111116 MGI PMID:16873689 1302055 Mob6_m multigenic obesity 6 (mouse) qtl MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16873689 1302055 Mob6_m multigenic obesity 6 (mouse) qtl MP:0005449 abnormal food intake IAGP N RGD:5509061 20111116 MGI PMID:16873689 1302055 Mob6_m multigenic obesity 6 (mouse) qtl MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20111116 MGI PMID:16873689 1302055 Mob6_m multigenic obesity 6 (mouse) qtl MP:0011582 decreased triglyceride lipase activity IAGP N RGD:5509061 20120209 MGI PMID:9616220 1302056 Orgwq4_m organ weight QTL 4 (mouse) qtl MP:0002833 increased heart weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1302056 Orgwq4_m organ weight QTL 4 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1302056 Orgwq4_m organ weight QTL 4 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1302056 Orgwq4_m organ weight QTL 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12118102 1302056 Orgwq4_m organ weight QTL 4 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1302058 Hrtfm3_m heart failure modifier 3 (mouse) qtl MP:0001661 extended life span IAGP N RGD:5509061 20111116 MGI PMID:14519689 1302058 Hrtfm3_m heart failure modifier 3 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14519689 1302060 El3_m epilepsy 3 (mouse) qtl MP:0002064 seizures IAGP N RGD:5509061 20111116 MGI PMID:8747920 1302060 El3_m epilepsy 3 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8747920 1302060 El3_m epilepsy 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8747920 1302061 Szv1_m seizure severity 1 (mouse) qtl MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20111116 MGI PMID:9069121 1302061 Szv1_m seizure severity 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9069121 1302061 Szv1_m seizure severity 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9069121 1302062 Stheal6_m soft tissue heal 6 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:11731492 1302062 Stheal6_m soft tissue heal 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11731492 1302063 Eae19_m experimental allergic encephalomyelitis 19 (mouse) qtl MP:0000921 demyelination IAGP N RGD:5509061 20111116 MGI PMID:10934166 1302063 Eae19_m experimental allergic encephalomyelitis 19 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10934166 1302064 Pbwg5_m postnatal body weight growth 5 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 1302064 Pbwg5_m postnatal body weight growth 5 (mouse) qtl MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20111116 MGI PMID:15056934 1302064 Pbwg5_m postnatal body weight growth 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15056934 1302065 El1_m epilepsy 1 (mouse) qtl MP:0002064 seizures IAGP N RGD:5509061 20111116 MGI PMID:1871601 1302065 El1_m epilepsy 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1871601 1302065 El1_m epilepsy 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1871601 1302066 Insq2_m insulin QTL 2 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:11109545 1302066 Insq2_m insulin QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11109545 1302067 Scc9_m colon tumor susceptibility 9 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10485458 1302067 Scc9_m colon tumor susceptibility 9 (mouse) qtl MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20111116 MGI PMID:10485458 1302067 Scc9_m colon tumor susceptibility 9 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:10485458 1302071 Fembrs1_m femur breaking strength 1 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:11991724 1302071 Fembrs1_m femur breaking strength 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11991724 1302072 Axtofa7_m anxiety-open field activity 7 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11454769|PMID:14990867 1302072 Axtofa7_m anxiety-open field activity 7 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160422 MGI Created by mouse qtl pipeline PMID:11418486|PMID:11454769 1302072 Axtofa7_m anxiety-open field activity 7 (mouse) qtl MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:14990867 1302073 Pgct1_m primordial germ cell tumor locus 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10890890 1302073 Pgct1_m primordial germ cell tumor locus 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:10890890 1302073 Pgct1_m primordial germ cell tumor locus 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:10890890 1302073 Pgct1_m primordial germ cell tumor locus 1 (mouse) qtl MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:10890890 1302075 Bdln6_m body length 6 (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20111116 MGI PMID:12856282 1302075 Bdln6_m body length 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12856282 1302078 Sluc21_m susceptibility to lung cancer 21 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1302078 Sluc21_m susceptibility to lung cancer 21 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1302078 Sluc21_m susceptibility to lung cancer 21 (mouse) qtl MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1302079 Lbw3_m lupus NZB x NZW 3 (mouse) qtl MP:0002083 premature death IAGP N RGD:5509061 20111116 MGI PMID:7937857 1302079 Lbw3_m lupus NZB x NZW 3 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7937857 1302080 Szs13_m seizure susceptibility 13 (mouse) qtl MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20111116 MGI PMID:11472065 1302080 Szs13_m seizure susceptibility 13 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1302080 Szs13_m seizure susceptibility 13 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1302084 Ckds_m cystic kidney disease severity (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11773599 1302084 Ckds_m cystic kidney disease severity (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:11773599 1302084 Ckds_m cystic kidney disease severity (mouse) qtl MP:0008528 polycystic kidney IAGP N RGD:5509061 20111116 MGI PMID:11773599 1302085 Mobe1_m modifier of obesity 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:14693723 1302085 Mobe1_m modifier of obesity 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14693723 1302086 Obq9_m obesity QTL 9 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:11210195 1302086 Obq9_m obesity QTL 9 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11210195 1302087 Axtofa5_m anxiety-open field activity 5 (mouse) qtl MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20111116 MGI PMID:14990867 1302087 Axtofa5_m anxiety-open field activity 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11454769|PMID:14990867 1302087 Axtofa5_m anxiety-open field activity 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160422 MGI Created by mouse qtl pipeline PMID:14990867 1302087 Axtofa5_m anxiety-open field activity 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160506 MGI Created by mouse qtl pipeline PMID:11454769 1302088 Gvhd2_m graft-versus-host disease 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10233703 1302088 Gvhd2_m graft-versus-host disease 2 (mouse) qtl MP:0005672 increased susceptibility to graft versus host disease IAGP N RGD:5509061 20111116 MGI PMID:10233703 1302089 Wta2_m weight adult 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11178736 1302089 Wta2_m weight adult 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1302090 Bdt3_m bone density traits 3 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:16200066 1302090 Bdt3_m bone density traits 3 (mouse) qtl MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16200066 1302090 Bdt3_m bone density traits 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11328966 1302090 Bdt3_m bone density traits 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11328966 1302090 Bdt3_m bone density traits 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11328966 1302090 Bdt3_m bone density traits 3 (mouse) qtl MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20111116 MGI PMID:16200066 1302090 Bdt3_m bone density traits 3 (mouse) qtl MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16200066 1302092 Ath11_m atherosclerosis 11 (mouse) qtl MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20111116 MGI PMID:11973313 1302092 Ath11_m atherosclerosis 11 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11973313 1302093 Orgwq5_m organ weight QTL 5 (mouse) qtl MP:0002834 decreased heart weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1302093 Orgwq5_m organ weight QTL 5 (mouse) qtl MP:0003918 decreased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1302093 Orgwq5_m organ weight QTL 5 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1302093 Orgwq5_m organ weight QTL 5 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1302094 Rrodp1_m rotarod performance 1 (mouse) qtl MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20111116 MGI PMID:14694905 1302094 Rrodp1_m rotarod performance 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14694905 1302096 Aod1a_m autoimmune ovarian dysgenesis 1a (mouse) qtl MP:0001868 ovary inflammation IAGP N RGD:5509061 20111116 MGI PMID:12794114 1302096 Aod1a_m autoimmune ovarian dysgenesis 1a (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12794114 1302096 Aod1a_m autoimmune ovarian dysgenesis 1a (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12794114 1302096 Aod1a_m autoimmune ovarian dysgenesis 1a (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12794114 1302098 Eila1_m ethanol induced locomotor activity 1 (mouse) qtl MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20111116 MGI PMID:12931787 1302098 Eila1_m ethanol induced locomotor activity 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12931787 1302099 Hdlq30_m HDL QTL 30 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14993241 1302099 Hdlq30_m HDL QTL 30 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14993241 1302100 Circp2_m circadian photosensitivity 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12465884 1302100 Circp2_m circadian photosensitivity 2 (mouse) qtl MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:12465884 1302102 Bis1_m beta-carboline-induced seizures 1 (mouse) qtl MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20111116 MGI PMID:10234005 1302102 Bis1_m beta-carboline-induced seizures 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10234005|PMID:7657995 1302102 Bis1_m beta-carboline-induced seizures 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10234005|PMID:7657995 1302103 Dob2_m dietary obesity 2 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:7929816 1302103 Dob2_m dietary obesity 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7929816 1302104 Lfp1_m long free running period 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309657 1302104 Lfp1_m long free running period 1 (mouse) qtl MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:11309657 1302105 Im1_m Immunoregulatory 1 (mouse) qtl MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20111116 MGI PMID:9472069 1302105 Im1_m Immunoregulatory 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9472069 1302106 Rapop1_m radiation-induced apoptosis 1 (mouse) qtl MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20111116 MGI PMID:9545495 1302106 Rapop1_m radiation-induced apoptosis 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9545495|PMID:9367689 1302106 Rapop1_m radiation-induced apoptosis 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:9545495 1302108 Skl5_m skeletal size (tail length) 5 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11178736 1302108 Skl5_m skeletal size (tail length) 5 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:11178736 1302108 Skl5_m skeletal size (tail length) 5 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1302108 Skl5_m skeletal size (tail length) 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1302109 Sluc28_m susceptibility to lung cancer 28 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 1302109 Sluc28_m susceptibility to lung cancer 28 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1302109 Sluc28_m susceptibility to lung cancer 28 (mouse) qtl MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:11584065 1302110 Szs12_m seizure susceptibility 12 (mouse) qtl MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20111116 MGI PMID:11472065 1302110 Szs12_m seizure susceptibility 12 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1302110 Szs12_m seizure susceptibility 12 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1302112 Gct_m granulosa cell tumorigenesis (mouse) qtl MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20131226 MGI PMID:9721880 1302113 Chol5_m cholesterol 5 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16679719 1302114 Tbs1_m tuberculosis severity 1 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:12496157 1302114 Tbs1_m tuberculosis severity 1 (mouse) qtl MP:0005150 cachexia IAGP N RGD:5509061 20111116 MGI PMID:12496157 1302114 Tbs1_m tuberculosis severity 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353873 1302114 Tbs1_m tuberculosis severity 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353873 1302116 Bbaa1_m B.burgdorferi-associated arthritis 1 (mouse) qtl MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:9916719 1302116 Bbaa1_m B.burgdorferi-associated arthritis 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9916719 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0001869 pancreas inflammation IAGP N RGD:5509061 20111116 MGI PMID:11016460 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0001869 pancreas inflammation IAGP N RGD:5509061 20111116 MGI PMID:8384947 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0001873 stomach inflammation IAGP N RGD:5509061 20111116 MGI PMID:16172259 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:10857762 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:10955330 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:11016460 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:1675432 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:18056379 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:8384947 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:9257847 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:9988264 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20111116 MGI PMID:16172259 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20111116 MGI PMID:12759418 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0004031 insulitis IAGP N RGD:5509061 20111116 MGI PMID:18056379 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20111116 MGI PMID:17277778 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20111116 MGI PMID:17277778 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10857762|PMID:17277778|PMID:1675432|PMID:11016460|PMID:9988264|PMID:7556956 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20180330 MGI Created by mouse qtl pipeline PMID:10857762|PMID:17277778|PMID:11016460|PMID:9988264|PMID:7556956 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10857762|PMID:17277778|PMID:1675432|PMID:11016460|PMID:9988264|PMID:7556956 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20180330 MGI Created by mouse qtl pipeline PMID:10857762|PMID:17277778|PMID:11016460|PMID:9988264|PMID:7556956 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10857762|PMID:17277778|PMID:1675432|PMID:11016460|PMID:9988264|PMID:7556956 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20180330 MGI Created by mouse qtl pipeline PMID:10857762|PMID:17277778|PMID:11016460|PMID:9988264|PMID:7556956 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10857762|PMID:17277778|PMID:1675432|PMID:11016460|PMID:9988264|PMID:7556956 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20180330 MGI Created by mouse qtl pipeline PMID:10857762|PMID:17277778|PMID:11016460|PMID:9988264|PMID:7556956 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:10857762|PMID:17277778|PMID:1675432|PMID:11016460|PMID:9988264|PMID:7556956 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20180330 MGI Created by mouse qtl pipeline PMID:10857762|PMID:17277778|PMID:11016460|PMID:9988264|PMID:7556956 1302117 Idd3_m insulin dependent diabetes susceptibility 3 (mouse) qtl MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20111116 MGI PMID:12759418 1302121 Cliff_m cliff drop aversion (mouse) qtl MP:0001961 abnormal reflex IAGP N RGD:5509061 20111116 MGI PMID:10086232 1302121 Cliff_m cliff drop aversion (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10086232 1302122 Eae8_m susceptibility to experimental allergic encephalomyelitis 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9712054|PMID:8757345 1302122 Eae8_m susceptibility to experimental allergic encephalomyelitis 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20131011 MGI Created by mouse qtl pipeline PMID:8757345|PMID:9712054 1302124 Eae7_m susceptibility to experimental allergic encephalomyelitis 7 (mouse) qtl MP:0001847 brain inflammation IAGP N RGD:5509061 20111116 MGI PMID:9712054 1302124 Eae7_m susceptibility to experimental allergic encephalomyelitis 7 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9712054 1302124 Eae7_m susceptibility to experimental allergic encephalomyelitis 7 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:9712054 1302124 Eae7_m susceptibility to experimental allergic encephalomyelitis 7 (mouse) qtl MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:9712054 1302124 Eae7_m susceptibility to experimental allergic encephalomyelitis 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9712054 1302125 Lxw1_m lupus BXSB x NZW 1 (mouse) qtl MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20111116 MGI PMID:14662843 1302125 Lxw1_m lupus BXSB x NZW 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14662843 1302126 Skull26_m skull morphology 26 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1302126 Skull26_m skull morphology 26 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1302126 Skull26_m skull morphology 26 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1302127 Hlq3_m heat loss QTL 3 (mouse) qtl MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20111116 MGI PMID:10353911 1302127 Hlq3_m heat loss QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1302128 Ity3_m immunity to S. typhimurium 3 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:17660555 1302128 Ity3_m immunity to S. typhimurium 3 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:9479490 1302128 Ity3_m immunity to S. typhimurium 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9479490 1302130 Fembm5_m femoral bone morphometry 5 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11518254 1302130 Fembm5_m femoral bone morphometry 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11518254 1302130 Fembm5_m femoral bone morphometry 5 (mouse) qtl MP:0030823 increased femur size IAGP N RGD:5509061 20181018 MGI PMID:11518254 1302131 Bmd8_m bone mineral density 8 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:12568393 1302131 Bmd8_m bone mineral density 8 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:14667144 1302131 Bmd8_m bone mineral density 8 (mouse) qtl MP:0004991 decreased bone strength IAGP N RGD:5509061 20111116 MGI PMID:14667144 1302131 Bmd8_m bone mineral density 8 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11450694 1302131 Bmd8_m bone mineral density 8 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11450694 1302131 Bmd8_m bone mineral density 8 (mouse) qtl MP:0013616 decreased volumetric bone mineral density IAGP N RGD:5509061 20220915 MGI PMID:14667144 1302131 Bmd8_m bone mineral density 8 (mouse) qtl MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:11450694 1302131 Bmd8_m bone mineral density 8 (mouse) qtl MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:12568393 1302132 Pbw1_m pentobarbital withdrawal QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10337613 1302132 Pbw1_m pentobarbital withdrawal QTL 1 (mouse) qtl MP:0009775 increased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:10337613 1302132 Pbw1_m pentobarbital withdrawal QTL 1 (mouse) qtl MP:0009776 decreased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:10337613 1302136 Insq3_m insulin QTL 3 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:11109545 1302136 Insq3_m insulin QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11109545 1302137 Livq1_m percent liver QTL 1 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:10353911 1302137 Livq1_m percent liver QTL 1 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1302137 Livq1_m percent liver QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:10353911 1302138 Im6_m immunoregulatory 6 (mouse) qtl MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20111116 MGI PMID:8962125 1302138 Im6_m immunoregulatory 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8962125 1302140 Wta4_m weight adult 4 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:11178736 1302140 Wta4_m weight adult 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11178736 1302141 Fcsa6_m femoral cross-sectional area 6 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12369778 1302141 Fcsa6_m femoral cross-sectional area 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12369778 1302141 Fcsa6_m femoral cross-sectional area 6 (mouse) qtl MP:0008158 increased diameter of femur IAGP N RGD:5509061 20111116 MGI PMID:12369778 1302143 Bwq5_m body weight (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:12856282 1302143 Bwq5_m body weight (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12856282 1302144 Oriq3_m ovulation rate QTL 3 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1302145 Triglq2_m triglyceride QTL 2 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:11109545 1302145 Triglq2_m triglyceride QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11109545 1302147 Skts12_m skin tumor susceptibility 12 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1302147 Skts12_m skin tumor susceptibility 12 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:7670492 1302147 Skts12_m skin tumor susceptibility 12 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1302150 Bbaa18_m B.burgdorferi-associated arthritis 18 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11704805 1302150 Bbaa18_m B.burgdorferi-associated arthritis 18 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11704805|PMID:11431140 1302151 Lprm2_m lymphoproliferation modifier 2 (mouse) qtl MP:0001864 vascular inflammation IAGP N RGD:5509061 20111116 MGI PMID:10940892 1302151 Lprm2_m lymphoproliferation modifier 2 (mouse) qtl MP:0001864 vascular inflammation IAGP N RGD:5509061 20111116 MGI PMID:9403730 1302151 Lprm2_m lymphoproliferation modifier 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10940892 1302151 Lprm2_m lymphoproliferation modifier 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10940892 1302152 Skull25_m skull morphology 25 (mouse) qtl MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1302152 Skull25_m skull morphology 25 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1302152 Skull25_m skull morphology 25 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1302153 Fob1_m F-line obesity QTL 1 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:10602985 1302153 Fob1_m F-line obesity QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10602985 1302154 Skmw5_m skeletal muscle weight 5 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:14679300 1302154 Skmw5_m skeletal muscle weight 5 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14679300 1302157 Bwem2_m body weight day 30 males 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:10086232 1302157 Bwem2_m body weight day 30 males 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10086232 1302158 Fembrs5_m femur breaking strength 5 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:11991724 1302158 Fembrs5_m femur breaking strength 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11991724 1302159 Sle8_m systematic lupus erythematosus susceptibility 8 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:10693874 1302159 Sle8_m systematic lupus erythematosus susceptibility 8 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10693874 1302159 Sle8_m systematic lupus erythematosus susceptibility 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10693874 1302160 Mbis2_m Mycobacterium bovis-induced systemic lupus erythematosus 2 (mouse) qtl MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:10903779 1302160 Mbis2_m Mycobacterium bovis-induced systemic lupus erythematosus 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10903779 1302163 Bmd16_m bone mineral density 16 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:12568393 1302163 Bmd16_m bone mineral density 16 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:14667144 1302163 Bmd16_m bone mineral density 16 (mouse) qtl MP:0004991 decreased bone strength IAGP N RGD:5509061 20111116 MGI PMID:14667144 1302163 Bmd16_m bone mineral density 16 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11450694 1302163 Bmd16_m bone mineral density 16 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11450694 1302163 Bmd16_m bone mineral density 16 (mouse) qtl MP:0010968 decreased compact bone area IAGP N RGD:5509061 20220922 MGI PMID:14667144 1302163 Bmd16_m bone mineral density 16 (mouse) qtl MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:11450694 1302163 Bmd16_m bone mineral density 16 (mouse) qtl MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:12568393 1302163 Bmd16_m bone mineral density 16 (mouse) qtl MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20220922 MGI PMID:11450694 1302163 Bmd16_m bone mineral density 16 (mouse) qtl MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20220922 MGI PMID:12568393 1302164 Psl2_m promotion susceptibility QTL 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12782578 1302164 Psl2_m promotion susceptibility QTL 2 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:12782578 1302164 Psl2_m promotion susceptibility QTL 2 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12782578 1302168 Imgt1_m impaired glucose tolerance 1 (mouse) qtl MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20111116 MGI PMID:11473059 1302168 Imgt1_m impaired glucose tolerance 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11473059 1302170 Tanidd1_m tally ho associated non-insulin dependednt diabetes mellitus 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15870394 1302170 Tanidd1_m tally ho associated non-insulin dependednt diabetes mellitus 1 (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:11414755 1302170 Tanidd1_m tally ho associated non-insulin dependednt diabetes mellitus 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11414755 1302170 Tanidd1_m tally ho associated non-insulin dependednt diabetes mellitus 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11414755 1302170 Tanidd1_m tally ho associated non-insulin dependednt diabetes mellitus 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11414755 1302170 Tanidd1_m tally ho associated non-insulin dependednt diabetes mellitus 1 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:15870394 1302170 Tanidd1_m tally ho associated non-insulin dependednt diabetes mellitus 1 (mouse) qtl MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15870394 1302172 Skts5_m skin tumor susceptibility 5 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1302172 Skts5_m skin tumor susceptibility 5 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:10611333 1302172 Skts5_m skin tumor susceptibility 5 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10611333 1302173 Vent1_m ventricular size 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12746874 1302173 Vent1_m ventricular size 1 (mouse) qtl MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20140220 MGI PMID:12746874 1302174 Dssc2_m dextran sodium sulfate induced colitis QTL2 (mouse) qtl MP:0002816 colitis IAGP N RGD:5509061 20111116 MGI PMID:9933561 1302174 Dssc2_m dextran sodium sulfate induced colitis QTL2 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9933561 1302174 Dssc2_m dextran sodium sulfate induced colitis QTL2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9933561 1302175 Dssc1_m dextran sodium sulfate induced colitis QTL1 (mouse) qtl MP:0002816 colitis IAGP N RGD:5509061 20111116 MGI PMID:9933561 1302175 Dssc1_m dextran sodium sulfate induced colitis QTL1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9933561 1302175 Dssc1_m dextran sodium sulfate induced colitis QTL1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9933561 1302176 Afw1_m abdominal fat weight QTL 1 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141016 MGI PMID:9725853 1302176 Afw1_m abdominal fat weight QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089|PMID:9725853 1302176 Afw1_m abdominal fat weight QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20141017 MGI Created by mouse qtl pipeline PMID:9725853 1302179 Mndl2_m mandible length 2 (mouse) qtl MP:0004593 long mandible IAGP N RGD:5509061 20111116 MGI PMID:12161465 1302179 Mndl2_m mandible length 2 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12161465 1302179 Mndl2_m mandible length 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12161465 1302180 Actd4_m activity-distance traveled 4 (mouse) qtl MP:0001399 hyperactivity IAGP N RGD:5509061 20111116 MGI PMID:11105390 1302180 Actd4_m activity-distance traveled 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11105390 1302182 Mob7_m multigenic obesity 7 (mouse) qtl MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:9616220 1302183 Pas7_m pulmonary adenoma susceptibility 7 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9790761 1302183 Pas7_m pulmonary adenoma susceptibility 7 (mouse) qtl MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20111116 MGI PMID:9790761 1302183 Pas7_m pulmonary adenoma susceptibility 7 (mouse) qtl MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20111116 MGI PMID:9790761 1302183 Pas7_m pulmonary adenoma susceptibility 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9790761 1302183 Pas7_m pulmonary adenoma susceptibility 7 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9790761 1302184 Aaom1_m autoimmune aoritis in MRL mice 1 (mouse) qtl MP:0001864 vascular inflammation IAGP N RGD:5509061 20111116 MGI PMID:12746919 1302184 Aaom1_m autoimmune aoritis in MRL mice 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12746919 1302184 Aaom1_m autoimmune aoritis in MRL mice 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12746919 1302185 Pkcal_m protein kinase C activity in lungs (mouse) qtl MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20111116 MGI PMID:10926556 1302185 Pkcal_m protein kinase C activity in lungs (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10926556 1302186 Blmpf2_m bleomycin-induced pulmonary fibrosis 2 (mouse) qtl MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20111116 MGI PMID:12140188 1302186 Blmpf2_m bleomycin-induced pulmonary fibrosis 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:12140188 1302186 Blmpf2_m bleomycin-induced pulmonary fibrosis 2 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12140188 1302186 Blmpf2_m bleomycin-induced pulmonary fibrosis 2 (mouse) qtl MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20111116 MGI PMID:12140188 1302188 Lxw6_m lupus BXSB x NZW 6 (mouse) qtl MP:0000691 enlarged spleen IAGP N RGD:5509061 20111116 MGI PMID:14662843 1302188 Lxw6_m lupus BXSB x NZW 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:14662843 1302188 Lxw6_m lupus BXSB x NZW 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14662843 1302188 Lxw6_m lupus BXSB x NZW 6 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14662843 1302191 Mtes1_m Metastasis efficiency suppressor gene 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11751410|PMID:15859357 1302191 Mtes1_m Metastasis efficiency suppressor gene 1 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:15859357 1302191 Mtes1_m Metastasis efficiency suppressor gene 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:11751410|PMID:15859357 1302191 Mtes1_m Metastasis efficiency suppressor gene 1 (mouse) qtl MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:11751410 1302191 Mtes1_m Metastasis efficiency suppressor gene 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:11751410|PMID:15859357 1302192 Tir2_m trypanosome infection response 2 (mouse) qtl MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20111116 MGI PMID:9171834 1302192 Tir2_m trypanosome infection response 2 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:15859356 1302192 Tir2_m trypanosome infection response 2 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:18253157 1302192 Tir2_m trypanosome infection response 2 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:9171834 1302192 Tir2_m trypanosome infection response 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9171834|PMID:12847546 1302192 Tir2_m trypanosome infection response 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20150626 MGI Created by mouse qtl pipeline PMID:9171834 1302193 Cpfd1_m cerebellum pattern fissures (mouse) qtl MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20111116 MGI PMID:11529272 1302193 Cpfd1_m cerebellum pattern fissures (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11529272 1302194 Pgia10_m proteoglycan induced arthritis 10 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10615997 1302194 Pgia10_m proteoglycan induced arthritis 10 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:10615997 1302194 Pgia10_m proteoglycan induced arthritis 10 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10615997 1302197 Bhr2_m bronchial hyperresponsiveness 2 (mouse) qtl MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20111116 MGI PMID:7550342 1302197 Bhr2_m bronchial hyperresponsiveness 2 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7550342 1302198 Lrncs1_m learning-conditioned stimulus 1 (mouse) qtl MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20111116 MGI PMID:9106670 1302198 Lrncs1_m learning-conditioned stimulus 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9106670 1302199 Mob3_m multigenic obesity 3 (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:7706460 1302200 Sle12_m systematic lupus erythematosus susceptibility 12 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:9922399 1302200 Sle12_m systematic lupus erythematosus susceptibility 12 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9922399 1302200 Sle12_m systematic lupus erythematosus susceptibility 12 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9922399 1302201 Alcw1_m alcohol withdrawal 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9133412 1302201 Alcw1_m alcohol withdrawal 1 (mouse) qtl MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20111116 MGI PMID:10443995 1302201 Alcw1_m alcohol withdrawal 1 (mouse) qtl MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20111116 MGI PMID:10443995 1302202 Dob3_m Dietary obesity 3 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:7929816 1302202 Dob3_m Dietary obesity 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7929816 1302203 Gvhd3_m graft-versus host disease 3 (mouse) qtl MP:0001263 weight loss IAGP N RGD:5509061 20111116 MGI PMID:10382959 1302203 Gvhd3_m graft-versus host disease 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10382959 1302204 Spm1_m splenomegaly modifier (mouse) qtl MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20111116 MGI PMID:10607744 1302204 Spm1_m splenomegaly modifier (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10607744 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:10441321 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:10678176 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10441321 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:10441321 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:10441321 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10678176 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10678176 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190801 MGI PMID:29360879 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:10678176 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10441321 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10678176 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0003199 calcified muscle IAGP N RGD:5509061 20141003 MGI PMID:10678176 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0003279 aneurysm IAGP N RGD:5509061 20141003 MGI PMID:10678176 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:10678176 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:10441321 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:10678176 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0005412 vascular stenosis IAGP N RGD:5509061 20141003 MGI PMID:10678176 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10678176 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:10678176 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:10441321 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:10441321 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:10441321 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0009421 increased gastrocnemius weight IAGP N RGD:5509061 20141003 MGI PMID:10441321 1312051 Sgcb sarcoglycan, beta (dystrophin-associated glycoprotein) gene MP:0009427 increased tibialis anterior weight IAGP N RGD:5509061 20141003 MGI PMID:10441321 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0000111 cleft palate IAGP N RGD:5509061 20230420 MGI PMID:27811357 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210128 MGI 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:17086203 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0002235 abnormal external nares morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0002243 abnormal vomeronasal organ morphology IAGP N RGD:5509061 20230420 MGI PMID:27811357 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20230420 MGI PMID:27811357 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0006290 proboscis IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0009654 abnormal primary palate development IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20230420 MGI PMID:27811357 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20230420 MGI PMID:27811357 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20221201 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20230420 MGI PMID:27811357 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0009897 decreased maxillary shelf size IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0009909 bifid tongue IAGP N RGD:5509061 20230420 MGI PMID:27811357 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0012523 abnormal upper lip morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0013788 external nares atresia IAGP N RGD:5509061 20150611 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0014276 lobar holoprosencephaly IAGP N RGD:5509061 20230810 MGI PMID:21183473 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230420 MGI PMID:27811357 1312052 Boc BOC cell adhesion associated, oncogene regulated gene MP:0030314 absent primary palate IAGP N RGD:5509061 20171109 MGI PMID:21183473 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:19893577 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0002492 decreased IgE level IEA N RGD:5509061 20160804 MGI 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20141003 MGI 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20141003 MGI 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:19897489 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20170413 MGI PMID:19893577 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:19897489 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:19897489 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19897489 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20160804 MGI 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0005316 abnormal response to tactile stimuli IEA N RGD:5509061 20141003 MGI 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20160804 MGI 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19897489 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0008210 increased mature B cell number IEA N RGD:5509061 20160804 MGI 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0008495 decreased IgG1 level IEA N RGD:5509061 20160804 MGI 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20170413 MGI PMID:19893577 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:19897489 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20170413 MGI PMID:19893577 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20170413 MGI PMID:19893577 1312055 Arhgef4 Rho guanine nucleotide exchange factor 4 gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20170413 MGI PMID:19893577 1312057 Ifi35 interferon-induced protein 35 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20211021 MGI PMID:29038465 1312057 Ifi35 interferon-induced protein 35 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20211021 MGI PMID:29038465 1312057 Ifi35 interferon-induced protein 35 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20211021 MGI PMID:29038465 1312057 Ifi35 interferon-induced protein 35 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20211021 MGI PMID:29038465 1312060 Cog3 component of oligomeric golgi complex 3 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1312060 Cog3 component of oligomeric golgi complex 3 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1312060 Cog3 component of oligomeric golgi complex 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312064 Pglyrp3 peptidoglycan recognition protein 3 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20709292 1312064 Pglyrp3 peptidoglycan recognition protein 3 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20709292 1312064 Pglyrp3 peptidoglycan recognition protein 3 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:20709292 1312064 Pglyrp3 peptidoglycan recognition protein 3 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:20709292 1312064 Pglyrp3 peptidoglycan recognition protein 3 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:20709292 1312064 Pglyrp3 peptidoglycan recognition protein 3 gene MP:0001262 decreased body weight IEA N RGD:5509061 20240523 MGI 1312064 Pglyrp3 peptidoglycan recognition protein 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20709292 1312064 Pglyrp3 peptidoglycan recognition protein 3 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20240523 MGI 1312064 Pglyrp3 peptidoglycan recognition protein 3 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20709292 1312064 Pglyrp3 peptidoglycan recognition protein 3 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20709292 1312064 Pglyrp3 peptidoglycan recognition protein 3 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20709292 1312064 Pglyrp3 peptidoglycan recognition protein 3 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20709292 1312064 Pglyrp3 peptidoglycan recognition protein 3 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20709292 1312064 Pglyrp3 peptidoglycan recognition protein 3 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20141003 MGI PMID:20709292 1312066 Dstn destrin gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20190502 MGI 1312066 Dstn destrin gene MP:0000274 enlarged heart IEA N RGD:5509061 20190502 MGI 1312066 Dstn destrin gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8603845 1312066 Dstn destrin gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:8603845 1312066 Dstn destrin gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:17875668 1312066 Dstn destrin gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:18628996 1312066 Dstn destrin gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:23406901 1312066 Dstn destrin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17875668 1312066 Dstn destrin gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:23406901 1312066 Dstn destrin gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:12700171 1312066 Dstn destrin gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:15855638 1312066 Dstn destrin gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:17051153 1312066 Dstn destrin gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:18628996 1312066 Dstn destrin gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:8603845 1312066 Dstn destrin gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15855638 1312066 Dstn destrin gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12700171 1312066 Dstn destrin gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17051153 1312066 Dstn destrin gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8603845 1312066 Dstn destrin gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:23406901 1312066 Dstn destrin gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15855638 1312066 Dstn destrin gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23406901 1312066 Dstn destrin gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1312066 Dstn destrin gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1312066 Dstn destrin gene MP:0020854 increased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:8603845 1312066 Dstn destrin gene MP:0020857 cornea epithelium hyperplasia IAGP N RGD:5509061 20181101 MGI PMID:11182022 1312066 Dstn destrin gene MP:0020857 cornea epithelium hyperplasia IAGP N RGD:5509061 20181101 MGI PMID:12700171 1312068 Wnt6 wingless-type MMTV integration site family, member 6 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23175771 1312068 Wnt6 wingless-type MMTV integration site family, member 6 gene MP:0001727 abnormal embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:23175771 1312068 Wnt6 wingless-type MMTV integration site family, member 6 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23175771 1312068 Wnt6 wingless-type MMTV integration site family, member 6 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:23175771 1312068 Wnt6 wingless-type MMTV integration site family, member 6 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:23175771 1312068 Wnt6 wingless-type MMTV integration site family, member 6 gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23175771 1312068 Wnt6 wingless-type MMTV integration site family, member 6 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20201022 MGI 1312068 Wnt6 wingless-type MMTV integration site family, member 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170105 MGI 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11151768 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23892475 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23892475 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12107726 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11151768 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22318952 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23892475 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0004130 abnormal muscle cell glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:23892475 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18931681 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:18931681 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:23892475 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:23892475 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18931681 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23892475 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:23892475 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0010951 abnormal lipid oxidation IAGP N RGD:5509061 20141003 MGI PMID:23892475 1312071 Tbc1d1 TBC1 domain family, member 1 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:23892475 1312073 Syne3 spectrin repeat containing, nuclear envelope family member 3 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1312073 Syne3 spectrin repeat containing, nuclear envelope family member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20211125 MGI PMID:23761073 1312073 Syne3 spectrin repeat containing, nuclear envelope family member 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1312075 Rufy2 RUN and FYVE domain-containing 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1312077 Senp6 SUMO/sentrin specific peptidase 6 gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 1312079 Igsf9 immunoglobulin superfamily, member 9 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1312079 Igsf9 immunoglobulin superfamily, member 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18268009 1312079 Igsf9 immunoglobulin superfamily, member 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150212 MGI PMID:24647940 1312079 Igsf9 immunoglobulin superfamily, member 9 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20150212 MGI PMID:24647940 1312079 Igsf9 immunoglobulin superfamily, member 9 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1312079 Igsf9 immunoglobulin superfamily, member 9 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20150212 MGI PMID:24647940 1312079 Igsf9 immunoglobulin superfamily, member 9 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1312079 Igsf9 immunoglobulin superfamily, member 9 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:24647940 1312080 A430005L14Rik RIKEN cDNA A430005L14 gene gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20211021 MGI 1312080 A430005L14Rik RIKEN cDNA A430005L14 gene gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 1312080 A430005L14Rik RIKEN cDNA A430005L14 gene gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20231207 MGI 1312080 A430005L14Rik RIKEN cDNA A430005L14 gene gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1312082 P3h2 prolyl 3-hydroxylase 2 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20200514 MGI 1312082 P3h2 prolyl 3-hydroxylase 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1312082 P3h2 prolyl 3-hydroxylase 2 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141016 MGI PMID:24368846 1312082 P3h2 prolyl 3-hydroxylase 2 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20180809 MGI PMID:25645914 1312082 P3h2 prolyl 3-hydroxylase 2 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 1312082 P3h2 prolyl 3-hydroxylase 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1312082 P3h2 prolyl 3-hydroxylase 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141016 MGI PMID:24368846 1312082 P3h2 prolyl 3-hydroxylase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141016 MGI PMID:24368846 1312082 P3h2 prolyl 3-hydroxylase 2 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141016 MGI PMID:24368846 1312084 Fem1b fem 1 homolog b gene MP:0000666 decreased prostate gland duct number IAGP N RGD:5509061 20141003 MGI PMID:18816836 1312084 Fem1b fem 1 homolog b gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:16024793 1312084 Fem1b fem 1 homolog b gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16024793 1312084 Fem1b fem 1 homolog b gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16024793 1312090 Mast2 microtubule associated serine/threonine kinase 2 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 1312090 Mast2 microtubule associated serine/threonine kinase 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20150430 MGI 1312091 Selenon selenoprotein N gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:21131290 1312091 Selenon selenoprotein N gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23325319 1312091 Selenon selenoprotein N gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:23325319 1312091 Selenon selenoprotein N gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23325319 1312091 Selenon selenoprotein N gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20141003 MGI PMID:23325319 1312091 Selenon selenoprotein N gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21131290 1312091 Selenon selenoprotein N gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:23325319 1312091 Selenon selenoprotein N gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:23325319 1312091 Selenon selenoprotein N gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:21131290 1312091 Selenon selenoprotein N gene MP:0004609 vertebral fusion IEA N RGD:5509061 20141003 MGI 1312091 Selenon selenoprotein N gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23325319 1312091 Selenon selenoprotein N gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:21131290 1312091 Selenon selenoprotein N gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0009422 decreased gastrocnemius weight IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0009424 decreased extensor digitorum longus weight IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0009426 decreased soleus weight IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0009428 decreased tibialis anterior weight IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:23325319 1312091 Selenon selenoprotein N gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:21858002 1312091 Selenon selenoprotein N gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:23325319 1312091 Selenon selenoprotein N gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20141003 MGI PMID:23325319 1312091 Selenon selenoprotein N gene MP:0011045 decreased lung elastance IAGP N RGD:5509061 20141003 MGI PMID:23325319 1312091 Selenon selenoprotein N gene MP:0012107 enhanced exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:23325319 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:10700190 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:10700190 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10700190 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10700190 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:10700190 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19265138 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19223432 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19265138 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20190307 MGI PMID:25625206 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:10700190 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:10700190 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:19223432 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19223432 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19265138 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19223432 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10700190 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10700190 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20190307 MGI PMID:25625206 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19223432 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19265138 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19223432 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19265138 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19223432 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19223432 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19223432 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10700190 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10700190 1312093 Map3k3 mitogen-activated protein kinase kinase kinase 3 gene MP:0031593 decreased cardiac jelly amount IAGP N RGD:5509061 20240229 MGI PMID:25625206 1312096 Zfp13 zinc finger protein 13 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20160804 MGI 1312096 Zfp13 zinc finger protein 13 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20160804 MGI 1312098 Hsd17b14 hydroxysteroid (17-beta) dehydrogenase 14 gene MP:0001925 male infertility IEA N RGD:5509061 20170413 MGI 1312098 Hsd17b14 hydroxysteroid (17-beta) dehydrogenase 14 gene MP:0002687 oligozoospermia IEA N RGD:5509061 20170413 MGI 1312098 Hsd17b14 hydroxysteroid (17-beta) dehydrogenase 14 gene MP:0008500 increased IgG2a level IEA N RGD:5509061 20170413 MGI 1312098 Hsd17b14 hydroxysteroid (17-beta) dehydrogenase 14 gene MP:0010166 increased response to stress-induced hyperthermia IEA N RGD:5509061 20170413 MGI 1312098 Hsd17b14 hydroxysteroid (17-beta) dehydrogenase 14 gene MP:0013600 testis degeneration IEA N RGD:5509061 20170413 MGI 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:23109424 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23109424 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23109424 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:23109424 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:23109424 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0004262 abnormal physical strength IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:23109424 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:23109424 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:23109424 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0009422 decreased gastrocnemius weight IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0009428 decreased tibialis anterior weight IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23109424 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:22068590 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12391329 1312104 Mtm1 X-linked myotubular myopathy gene 1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:23109424 1312106 Ago4 argonaute RISC catalytic subunit 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22863743 1312106 Ago4 argonaute RISC catalytic subunit 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22863743 1312106 Ago4 argonaute RISC catalytic subunit 4 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:22863743 1312106 Ago4 argonaute RISC catalytic subunit 4 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22863743 1312106 Ago4 argonaute RISC catalytic subunit 4 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:22863743 1312106 Ago4 argonaute RISC catalytic subunit 4 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:22863743 1312115 Lpin2 lipin 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20160811 MGI 1312115 Lpin2 lipin 2 gene MP:0000745 tremors IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0001577 anemia IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20160421 MGI 1312115 Lpin2 lipin 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 1312115 Lpin2 lipin 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1312115 Lpin2 lipin 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 1312115 Lpin2 lipin 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20160811 MGI 1312115 Lpin2 lipin 2 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312115 Lpin2 lipin 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 1312115 Lpin2 lipin 2 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20160128 MGI PMID:22908270 1312117 Snapc2 small nuclear RNA activating complex, polypeptide 2 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20240926 MGI 1312117 Snapc2 small nuclear RNA activating complex, polypeptide 2 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20191205 MGI 1312117 Snapc2 small nuclear RNA activating complex, polypeptide 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20191205 MGI 1312117 Snapc2 small nuclear RNA activating complex, polypeptide 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312117 Snapc2 small nuclear RNA activating complex, polypeptide 2 gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20191205 MGI 1312117 Snapc2 small nuclear RNA activating complex, polypeptide 2 gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20191205 MGI 1312117 Snapc2 small nuclear RNA activating complex, polypeptide 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1312118 Rap1gap2 RAP1 GTPase activating protein 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1312118 Rap1gap2 RAP1 GTPase activating protein 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20201022 MGI 1312118 Rap1gap2 RAP1 GTPase activating protein 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20181227 MGI 1312118 Rap1gap2 RAP1 GTPase activating protein 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1312118 Rap1gap2 RAP1 GTPase activating protein 2 gene MP:0005655 increased aggression IEA N RGD:5509061 20181227 MGI 1312120 Art1 ADP-ribosyltransferase 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220519 MGI 1312120 Art1 ADP-ribosyltransferase 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1312120 Art1 ADP-ribosyltransferase 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1312120 Art1 ADP-ribosyltransferase 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1312120 Art1 ADP-ribosyltransferase 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1312120 Art1 ADP-ribosyltransferase 1 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20221215 MGI 1312120 Art1 ADP-ribosyltransferase 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1312120 Art1 ADP-ribosyltransferase 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20221215 MGI 1312120 Art1 ADP-ribosyltransferase 1 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20220519 MGI 1312120 Art1 ADP-ribosyltransferase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0001261 obese IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0005661 decreased circulating adrenaline level IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0009138 increased brown fat lipid droplet number IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0020103 decreased hepatic glucose production IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0020426 abnormal beige fat cell physiology IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0020867 increased lipogenesis IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0030020 decreased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0030761 increased adrenaline level IAGP N RGD:5509061 20200409 MGI PMID:29378832 1312121 C2cd5 C2 calcium-dependent domain containing 5 gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:29378832 1312124 Cog1 component of oligomeric golgi complex 1 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241010 MGI 1312124 Cog1 component of oligomeric golgi complex 1 gene MP:0002718 abnormal inner cell mass morphology IEA N RGD:5509061 20241010 MGI 1312124 Cog1 component of oligomeric golgi complex 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1312124 Cog1 component of oligomeric golgi complex 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1312126 Tmem268 transmembrane protein 268 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20240822 MGI PMID:38730209 1312126 Tmem268 transmembrane protein 268 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20240822 MGI PMID:38730209 1312126 Tmem268 transmembrane protein 268 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20240822 MGI PMID:38730209 1312126 Tmem268 transmembrane protein 268 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20240822 MGI PMID:38730209 1312126 Tmem268 transmembrane protein 268 gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20240822 MGI PMID:38730209 1312126 Tmem268 transmembrane protein 268 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20240822 MGI PMID:38730209 1312126 Tmem268 transmembrane protein 268 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20240822 MGI PMID:38730209 1312126 Tmem268 transmembrane protein 268 gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20240822 MGI PMID:38730209 1312126 Tmem268 transmembrane protein 268 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20240822 MGI PMID:38730209 1312126 Tmem268 transmembrane protein 268 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20240822 MGI PMID:38730209 1312126 Tmem268 transmembrane protein 268 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20240822 MGI PMID:38730209 1312126 Tmem268 transmembrane protein 268 gene MP:0012440 abnormal neutrophil cell number IAGP N RGD:5509061 20240822 MGI PMID:38730209 1312126 Tmem268 transmembrane protein 268 gene MP:0012441 abnormal monocyte cell number IAGP N RGD:5509061 20240822 MGI PMID:38730209 1312126 Tmem268 transmembrane protein 268 gene MP:0014431 increased chemokine level IAGP N RGD:5509061 20240822 MGI PMID:38730209 1312126 Tmem268 transmembrane protein 268 gene MP:0020212 impaired leukocyte migration IAGP N RGD:5509061 20240822 MGI PMID:38730209 1312127 Ccdc65 coiled-coil domain containing 65 gene MP:0000434 megacephaly IAGP N RGD:5509061 20240307 MGI PMID:35844805 1312127 Ccdc65 coiled-coil domain containing 65 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240307 MGI PMID:35844805 1312127 Ccdc65 coiled-coil domain containing 65 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20240307 MGI PMID:35844805 1312127 Ccdc65 coiled-coil domain containing 65 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20240307 MGI PMID:35844805 1312127 Ccdc65 coiled-coil domain containing 65 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20240307 MGI PMID:35844805 1312127 Ccdc65 coiled-coil domain containing 65 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20240307 MGI PMID:35844805 1312127 Ccdc65 coiled-coil domain containing 65 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20240307 MGI PMID:35844805 1312127 Ccdc65 coiled-coil domain containing 65 gene MP:0009709 hydrometra IEA N RGD:5509061 20210128 MGI 1312127 Ccdc65 coiled-coil domain containing 65 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20240307 MGI PMID:35844805 1312127 Ccdc65 coiled-coil domain containing 65 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240307 MGI PMID:35844805 1312127 Ccdc65 coiled-coil domain containing 65 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1312127 Ccdc65 coiled-coil domain containing 65 gene MP:0013907 abnormal cerebrospinal fluid flow IAGP N RGD:5509061 20240307 MGI PMID:35844805 1312129 Ndufa7 NADH:ubiquinone oxidoreductase subunit A7 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20230601 MGI 1312129 Ndufa7 NADH:ubiquinone oxidoreductase subunit A7 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20230601 MGI 1312132 Polrmt polymerase (RNA) mitochondrial (DNA directed) gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1312132 Polrmt polymerase (RNA) mitochondrial (DNA directed) gene MP:0001891 hydrocephaly IEA N RGD:5509061 20210128 MGI 1312132 Polrmt polymerase (RNA) mitochondrial (DNA directed) gene MP:0002083 premature death IAGP N RGD:5509061 20180412 MGI PMID:27532055 1312132 Polrmt polymerase (RNA) mitochondrial (DNA directed) gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210128 MGI 1312132 Polrmt polymerase (RNA) mitochondrial (DNA directed) gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1312132 Polrmt polymerase (RNA) mitochondrial (DNA directed) gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20180412 MGI PMID:27532055 1312132 Polrmt polymerase (RNA) mitochondrial (DNA directed) gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20180412 MGI PMID:27532055 1312132 Polrmt polymerase (RNA) mitochondrial (DNA directed) gene MP:0003929 decreased heart rate variability IAGP N RGD:5509061 20180412 MGI PMID:27532055 1312132 Polrmt polymerase (RNA) mitochondrial (DNA directed) gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20180412 MGI PMID:27532055 1312132 Polrmt polymerase (RNA) mitochondrial (DNA directed) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180412 MGI PMID:27532055 1312132 Polrmt polymerase (RNA) mitochondrial (DNA directed) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1312132 Polrmt polymerase (RNA) mitochondrial (DNA directed) gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20180412 MGI PMID:27532055 1312136 Crtam cytotoxic and regulatory T cell molecule gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18329370 1312136 Crtam cytotoxic and regulatory T cell molecule gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18329370 1312136 Crtam cytotoxic and regulatory T cell molecule gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:19752223 1312136 Crtam cytotoxic and regulatory T cell molecule gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18329370 1312136 Crtam cytotoxic and regulatory T cell molecule gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18329370 1312136 Crtam cytotoxic and regulatory T cell molecule gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:18329370 1312136 Crtam cytotoxic and regulatory T cell molecule gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18329370 1312136 Crtam cytotoxic and regulatory T cell molecule gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18329370 1312136 Crtam cytotoxic and regulatory T cell molecule gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18329370 1312136 Crtam cytotoxic and regulatory T cell molecule gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:18329370 1312136 Crtam cytotoxic and regulatory T cell molecule gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:18329370 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11134350 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:11134350 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0008510 absent retina ganglion layer IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11134350 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312138 Nrf1 nuclear respiratory factor 1 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200116 MGI PMID:30333037 1312143 Agr2 anterior gradient 2 gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:19359471 1312143 Agr2 anterior gradient 2 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20231228 MGI PMID:25666625 1312143 Agr2 anterior gradient 2 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20025862 1312143 Agr2 anterior gradient 2 gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:19359471 1312143 Agr2 anterior gradient 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:19359471 1312143 Agr2 anterior gradient 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20231228 MGI PMID:25666625 1312143 Agr2 anterior gradient 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20025862 1312143 Agr2 anterior gradient 2 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:20025862 1312143 Agr2 anterior gradient 2 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20025862 1312143 Agr2 anterior gradient 2 gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:20025862 1312143 Agr2 anterior gradient 2 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:19359471 1312143 Agr2 anterior gradient 2 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20025862 1312143 Agr2 anterior gradient 2 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20025862 1312143 Agr2 anterior gradient 2 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20141003 MGI PMID:20025862 1312143 Agr2 anterior gradient 2 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0010799 stomach mucosa hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0010803 abnormal stomach enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23209296 1312143 Agr2 anterior gradient 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20231228 MGI PMID:25666625 1312143 Agr2 anterior gradient 2 gene MP:0013485 increased Paneth cell number IAGP N RGD:5509061 20150312 MGI PMID:20025862 1312144 Tmem216 transmembrane protein 216 gene MP:0000111 cleft palate IAGP N RGD:5509061 20240328 MGI PMID:38261656 1312144 Tmem216 transmembrane protein 216 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20240328 MGI PMID:38261656 1312144 Tmem216 transmembrane protein 216 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20240328 MGI PMID:38261656 1312144 Tmem216 transmembrane protein 216 gene MP:0002639 micrognathia IAGP N RGD:5509061 20240328 MGI PMID:38261656 1312144 Tmem216 transmembrane protein 216 gene MP:0003052 omphalocele IAGP N RGD:5509061 20240328 MGI PMID:38261656 1312144 Tmem216 transmembrane protein 216 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20240328 MGI PMID:38261656 1312144 Tmem216 transmembrane protein 216 gene MP:0004320 split sternum IAGP N RGD:5509061 20240328 MGI PMID:38261656 1312144 Tmem216 transmembrane protein 216 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20240328 MGI PMID:38261656 1312144 Tmem216 transmembrane protein 216 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20240328 MGI PMID:38261656 1312144 Tmem216 transmembrane protein 216 gene MP:0009744 postaxial polydactyly IAGP N RGD:5509061 20240328 MGI PMID:38261656 1312144 Tmem216 transmembrane protein 216 gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20240328 MGI PMID:38261656 1312144 Tmem216 transmembrane protein 216 gene MP:0011065 abnormal kidney epithelial cell primary cilium morphology IAGP N RGD:5509061 20240328 MGI PMID:38261656 1312144 Tmem216 transmembrane protein 216 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20240328 MGI PMID:38261656 1312144 Tmem216 transmembrane protein 216 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20240328 MGI PMID:38261656 1312144 Tmem216 transmembrane protein 216 gene MP:0020383 decreased kidney epithelial cell primary cilium length IAGP N RGD:5509061 20240328 MGI PMID:38261656 1312145 Tecrl trans-2,3-enoyl-CoA reductase-like gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 1312145 Tecrl trans-2,3-enoyl-CoA reductase-like gene MP:0003674 oxidative stress IAGP N RGD:5509061 20240822 MGI PMID:35577932 1312145 Tecrl trans-2,3-enoyl-CoA reductase-like gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20240822 MGI PMID:35577932 1312145 Tecrl trans-2,3-enoyl-CoA reductase-like gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20240822 MGI PMID:35577932 1312145 Tecrl trans-2,3-enoyl-CoA reductase-like gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1312145 Tecrl trans-2,3-enoyl-CoA reductase-like gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20240822 MGI PMID:35577932 1312145 Tecrl trans-2,3-enoyl-CoA reductase-like gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20240822 MGI PMID:35577932 1312145 Tecrl trans-2,3-enoyl-CoA reductase-like gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240822 MGI PMID:35577932 1312145 Tecrl trans-2,3-enoyl-CoA reductase-like gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240822 MGI PMID:35577932 1312147 Actr6 ARP6 actin-related protein 6 gene MP:0003443 increased circulating glycerol level IEA N RGD:5509061 20211021 MGI 1312147 Actr6 ARP6 actin-related protein 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312149 Atg14 autophagy related 14 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24185898 1312149 Atg14 autophagy related 14 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1312149 Atg14 autophagy related 14 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 1312149 Atg14 autophagy related 14 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 1312149 Atg14 autophagy related 14 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1312149 Atg14 autophagy related 14 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1312149 Atg14 autophagy related 14 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1312149 Atg14 autophagy related 14 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1312153 Rasgrp3 RAS, guanyl releasing protein 3 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20200514 MGI 1312153 Rasgrp3 RAS, guanyl releasing protein 3 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:16301621 1312153 Rasgrp3 RAS, guanyl releasing protein 3 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16301621 1312153 Rasgrp3 RAS, guanyl releasing protein 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200514 MGI 1312153 Rasgrp3 RAS, guanyl releasing protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15572660 1312153 Rasgrp3 RAS, guanyl releasing protein 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16301621 1312153 Rasgrp3 RAS, guanyl releasing protein 3 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20201022 MGI 1312153 Rasgrp3 RAS, guanyl releasing protein 3 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:16301621 1312153 Rasgrp3 RAS, guanyl releasing protein 3 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16301621 1312153 Rasgrp3 RAS, guanyl releasing protein 3 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16301621 1312153 Rasgrp3 RAS, guanyl releasing protein 3 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20200514 MGI 1312153 Rasgrp3 RAS, guanyl releasing protein 3 gene MP:0009453 enhanced contextual conditioning behavior IEA N RGD:5509061 20240523 MGI 1312153 Rasgrp3 RAS, guanyl releasing protein 3 gene MP:0013436 increased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20211021 MGI 1312155 Epha6 Eph receptor A6 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1312155 Epha6 Eph receptor A6 gene MP:0000599 enlarged liver IEA N RGD:5509061 20210128 MGI 1312155 Epha6 Eph receptor A6 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20170105 MGI 1312155 Epha6 Eph receptor A6 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18450376 1312155 Epha6 Eph receptor A6 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:18450376 1312155 Epha6 Eph receptor A6 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18450376 1312155 Epha6 Eph receptor A6 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20170105 MGI 1312155 Epha6 Eph receptor A6 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170105 MGI 1312155 Epha6 Eph receptor A6 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170105 MGI 1312155 Epha6 Eph receptor A6 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20170105 MGI 1312155 Epha6 Eph receptor A6 gene MP:0020340 abnormal inhibitory learning IAGP N RGD:5509061 20160915 MGI PMID:18450376 1312159 Nop2 NOP2 nucleolar protein gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20160421 MGI PMID:18405070 1312160 Med12l mediator complex subunit 12-like gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20201022 MGI 1312160 Med12l mediator complex subunit 12-like gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1312160 Med12l mediator complex subunit 12-like gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1312160 Med12l mediator complex subunit 12-like gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1312160 Med12l mediator complex subunit 12-like gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1312160 Med12l mediator complex subunit 12-like gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210826 MGI 1312162 Kdelr2 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 2 gene MP:0000111 cleft palate IEA N RGD:5509061 20210520 MGI 1312162 Kdelr2 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 2 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20200402 MGI 1312162 Kdelr2 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20190502 MGI 1312162 Kdelr2 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1312164 Ago1 argonaute RISC catalytic subunit 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:22474261 1312164 Ago1 argonaute RISC catalytic subunit 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:22474261 1312164 Ago1 argonaute RISC catalytic subunit 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:22474261 1312164 Ago1 argonaute RISC catalytic subunit 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1312164 Ago1 argonaute RISC catalytic subunit 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160804 MGI 1312164 Ago1 argonaute RISC catalytic subunit 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22474261 1312164 Ago1 argonaute RISC catalytic subunit 1 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:22474261 1312164 Ago1 argonaute RISC catalytic subunit 1 gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:22474261 1312164 Ago1 argonaute RISC catalytic subunit 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:22474261 1312164 Ago1 argonaute RISC catalytic subunit 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1312164 Ago1 argonaute RISC catalytic subunit 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:22474261 1312164 Ago1 argonaute RISC catalytic subunit 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1312165 Rabgap1l RAB GTPase activating protein 1-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:10585558 1312169 2700097O09Rik RIKEN cDNA 2700097O09 gene gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1312169 2700097O09Rik RIKEN cDNA 2700097O09 gene gene MP:0001513 limb grasping IEA N RGD:5509061 20181227 MGI 1312169 2700097O09Rik RIKEN cDNA 2700097O09 gene gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1312169 2700097O09Rik RIKEN cDNA 2700097O09 gene gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1312169 2700097O09Rik RIKEN cDNA 2700097O09 gene gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 1312169 2700097O09Rik RIKEN cDNA 2700097O09 gene gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1312171 Map3k6 mitogen-activated protein kinase kinase kinase 6 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:19214184 1312171 Map3k6 mitogen-activated protein kinase kinase kinase 6 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19214184 1312171 Map3k6 mitogen-activated protein kinase kinase kinase 6 gene MP:0009581 decreased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19214184 1312177 Fnip1 folliculin interacting protein 1 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20161124 MGI PMID:27303042 1312177 Fnip1 folliculin interacting protein 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20161124 MGI PMID:27303042 1312177 Fnip1 folliculin interacting protein 1 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:22709692 1312177 Fnip1 folliculin interacting protein 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0000706 small thymus IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22608497 1312177 Fnip1 folliculin interacting protein 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20161124 MGI PMID:27303042 1312177 Fnip1 folliculin interacting protein 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20161124 MGI PMID:27303042 1312177 Fnip1 folliculin interacting protein 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20161124 MGI PMID:27303042 1312177 Fnip1 folliculin interacting protein 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20170525 MGI PMID:25775561 1312177 Fnip1 folliculin interacting protein 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22608497 1312177 Fnip1 folliculin interacting protein 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22709692 1312177 Fnip1 folliculin interacting protein 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22608497 1312177 Fnip1 folliculin interacting protein 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22608497 1312177 Fnip1 folliculin interacting protein 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20161124 MGI PMID:27303042 1312177 Fnip1 folliculin interacting protein 1 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20170525 MGI PMID:25775561 1312177 Fnip1 folliculin interacting protein 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20170525 MGI PMID:25775561 1312177 Fnip1 folliculin interacting protein 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20170525 MGI PMID:25775561 1312177 Fnip1 folliculin interacting protein 1 gene MP:0002144 abnormal B cell differentiation IEA N RGD:5509061 20190418 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0002311 abnormal inspiratory capacity IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22608497 1312177 Fnip1 folliculin interacting protein 1 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:22608497 1312177 Fnip1 folliculin interacting protein 1 gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0002981 increased liver weight IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20170525 MGI PMID:25775561 1312177 Fnip1 folliculin interacting protein 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20170525 MGI PMID:25775561 1312177 Fnip1 folliculin interacting protein 1 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20231207 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20181011 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22608497 1312177 Fnip1 folliculin interacting protein 1 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22709692 1312177 Fnip1 folliculin interacting protein 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22709692 1312177 Fnip1 folliculin interacting protein 1 gene MP:0005015 increased T cell number IEA N RGD:5509061 20181011 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22709692 1312177 Fnip1 folliculin interacting protein 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:22608497 1312177 Fnip1 folliculin interacting protein 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20170525 MGI PMID:25775561 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:22608497 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:22709692 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008071 absent B cells IAGP N RGD:5509061 20161124 MGI PMID:27303042 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008082 increased single-positive T cell number IEA N RGD:5509061 20181011 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20161124 MGI PMID:27303042 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22709692 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:22709692 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008205 absent B-2 B cells IAGP N RGD:5509061 20141003 MGI PMID:22709692 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22709692 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22709692 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22709692 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20161124 MGI PMID:27303042 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22608497 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:22608497 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20170525 MGI PMID:25775561 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22608497 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22709692 1312177 Fnip1 folliculin interacting protein 1 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0009332 abnormal splenocyte morphology IAGP N RGD:5509061 20161124 MGI PMID:27303042 1312177 Fnip1 folliculin interacting protein 1 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0010294 increased kidney tumor incidence IAGP N RGD:5509061 20170525 MGI PMID:25775561 1312177 Fnip1 folliculin interacting protein 1 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20161124 MGI PMID:27303042 1312177 Fnip1 folliculin interacting protein 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:22608497 1312177 Fnip1 folliculin interacting protein 1 gene MP:0010511 shortened PR interval IAGP N RGD:5509061 20161124 MGI PMID:27303042 1312177 Fnip1 folliculin interacting protein 1 gene MP:0010574 dilated aorta IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0010895 increased lung compliance IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0010936 decreased airway resistance IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0011045 decreased lung elastance IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0011048 decreased lung tissue damping IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170525 MGI PMID:25775561 1312177 Fnip1 folliculin interacting protein 1 gene MP:0011951 increased cardiac stroke volume IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20161124 MGI PMID:27303042 1312177 Fnip1 folliculin interacting protein 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20240523 MGI 1312177 Fnip1 folliculin interacting protein 1 gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20190711 MGI PMID:27303042 1312181 Socs6 suppressor of cytokine signaling 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12052866 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:8934568 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8934568 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8934568 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8934568 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8934568 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8934568 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:8934568 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0001805 decreased IgG level IEA N RGD:5509061 20150305 MGI 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8934568 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18313334 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8934568 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18313334 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8934568 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18313334 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18313334 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18313334 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18313334 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18313334 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008211 decreased mature B cell number IEA N RGD:5509061 20141003 MGI 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17723217 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17015635 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8934568 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20150305 MGI 1312183 Traf3 TNF receptor-associated factor 3 gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20141003 MGI 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:15277503 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:17409257 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:23360997 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:15277503 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:23360997 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:15277503 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:15780988 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15780988 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15277503 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:23360997 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15277503 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15277503 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23360997 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:15277503 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15780988 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15277503 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:15780988 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15780988 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15277503 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15277503 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15277503 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:15277503 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15277503 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:17409257 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:23360997 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:17409257 1312189 Sema4a sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:23360997 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17554302 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10911993 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9823897 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:19171781 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:12531011 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:9823897 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10911993 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000727 absent CD8-positive, alpha-beta T cells IEA N RGD:5509061 20111116 MGI 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:19171781 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10716994 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:19171781 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10911993 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11040211 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17554302 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19171781 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17554302 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10911993 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9823897 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:9823897 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19171781 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10911993 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16777961 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19164512 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9823897 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10911993 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:19171781 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9823897 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:17554302 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002491 decreased IgD level IEA N RGD:5509061 20190110 MGI 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12531011 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10911993 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11040211 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16777961 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9889105 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10911993 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11040211 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16777961 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:19164512 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:19164512 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:12531011 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:17713479 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:18854157 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:10716994 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:9823897 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:10911993 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17713479 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:18854157 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:19171781 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:17554302 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:17713479 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:20133803 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004941 abnormal regulatory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10911993 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17554302 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17554302 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:10716994 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10716994 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9823897 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:10716994 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19164512 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0008044 increased NK cell number IEA N RGD:5509061 20190110 MGI 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:17554302 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:19171781 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190110 MGI 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0008758 abnormal T cell receptor beta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:18854157 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:20133615 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190110 MGI 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20190110 MGI 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20161013 MGI PMID:26290337 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11040211 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16777961 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19171781 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19171781 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16777961 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10911993 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12531011 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19171781 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20170413 MGI PMID:27798842 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9889105 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10911993 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12531011 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17554302 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9823897 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:10911993 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:17554302 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10911993 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0012504 increased forebrain apoptosis IAGP N RGD:5509061 20160428 MGI PMID:10716994 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0013182 increased spinal cord apoptosis IAGP N RGD:5509061 20160428 MGI PMID:10716994 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20190110 MGI 1312195 Lig4 ligase IV, DNA, ATP-dependent gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20190110 MGI 1312199 Stim2 stromal interaction molecule 2 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:21530328 1312199 Stim2 stromal interaction molecule 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 1312199 Stim2 stromal interaction molecule 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1312199 Stim2 stromal interaction molecule 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19843959 1312199 Stim2 stromal interaction molecule 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 1312199 Stim2 stromal interaction molecule 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19843959 1312199 Stim2 stromal interaction molecule 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0002221 abnormal lymph organ size IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21530328 1312199 Stim2 stromal interaction molecule 2 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19843959 1312199 Stim2 stromal interaction molecule 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1312199 Stim2 stromal interaction molecule 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1312199 Stim2 stromal interaction molecule 2 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21530328 1312199 Stim2 stromal interaction molecule 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19843959 1312199 Stim2 stromal interaction molecule 2 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21530328 1312199 Stim2 stromal interaction molecule 2 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21530328 1312199 Stim2 stromal interaction molecule 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:19843959 1312199 Stim2 stromal interaction molecule 2 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:19843959 1312199 Stim2 stromal interaction molecule 2 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20181227 MGI 1312199 Stim2 stromal interaction molecule 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21530328 1312199 Stim2 stromal interaction molecule 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21530328 1312199 Stim2 stromal interaction molecule 2 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0008407 decreased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:21746875 1312199 Stim2 stromal interaction molecule 2 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:21530328 1312199 Stim2 stromal interaction molecule 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21530328 1312199 Stim2 stromal interaction molecule 2 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21530328 1312199 Stim2 stromal interaction molecule 2 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:21530328 1312199 Stim2 stromal interaction molecule 2 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:18327260 1312199 Stim2 stromal interaction molecule 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20181227 MGI 1312199 Stim2 stromal interaction molecule 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19843959 1312199 Stim2 stromal interaction molecule 2 gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:21530328 1312201 Foxd2 forkhead box D2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:10648626 1312201 Foxd2 forkhead box D2 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:10648626 1312201 Foxd2 forkhead box D2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1312201 Foxd2 forkhead box D2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1312201 Foxd2 forkhead box D2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1312201 Foxd2 forkhead box D2 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20240523 MGI 1312201 Foxd2 forkhead box D2 gene MP:0002764 short tibia IEA N RGD:5509061 20240523 MGI 1312201 Foxd2 forkhead box D2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:10648626 1312201 Foxd2 forkhead box D2 gene MP:0002990 short ureter IAGP N RGD:5509061 20141003 MGI PMID:10648626 1312201 Foxd2 forkhead box D2 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20240523 MGI 1312201 Foxd2 forkhead box D2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1312202 Aste1 asteroid homolog 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20160804 MGI 1312202 Aste1 asteroid homolog 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20190926 MGI PMID:26660539 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190926 MGI PMID:26660539 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0001505 hunched posture IAGP N RGD:5509061 20190926 MGI PMID:26660539 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20190926 MGI PMID:26660539 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20160804 MGI 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0002764 short tibia IAGP N RGD:5509061 20190926 MGI PMID:26660539 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0002931 glutaricadicuria IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0003109 short femur IAGP N RGD:5509061 20190926 MGI PMID:26660539 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0004019 abnormal vitamin homeostasis IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0004265 abnormal placental transport IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20190926 MGI PMID:26660539 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0005202 lethargy IAGP N RGD:5509061 20190926 MGI PMID:26660539 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0005400 abnormal vitamin level IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0005400 abnormal vitamin level IAGP N RGD:5509061 20190926 MGI PMID:26660539 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20190926 MGI PMID:26660539 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0013754 abnormal ocular surface morphology IAGP N RGD:5509061 20190926 MGI PMID:26660539 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0014174 decreased fatty acid beta-oxidation IAGP N RGD:5509061 20161222 MGI PMID:27272163 1312204 Slc52a3 solute carrier protein family 52, member 3 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:26660539 1312207 Dis3 DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1312207 Dis3 DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease gene MP:0001488 increased startle reflex IEA N RGD:5509061 20190502 MGI 1312207 Dis3 DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1312207 Dis3 DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20210513 MGI PMID:33526923 1312207 Dis3 DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20210513 MGI PMID:33526923 1312207 Dis3 DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20210513 MGI PMID:33526923 1312207 Dis3 DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1312207 Dis3 DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1312207 Dis3 DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312209 Snx6 sorting nexin 6 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 1312209 Snx6 sorting nexin 6 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1312209 Snx6 sorting nexin 6 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1312209 Snx6 sorting nexin 6 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20191114 MGI PMID:28134614 1312209 Snx6 sorting nexin 6 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20191114 MGI PMID:28134614 1312209 Snx6 sorting nexin 6 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20191114 MGI PMID:28134614 1312209 Snx6 sorting nexin 6 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20191114 MGI PMID:28134614 1312209 Snx6 sorting nexin 6 gene MP:0020360 abnormal asymmetric synapse morphology IAGP N RGD:5509061 20191114 MGI PMID:28134614 1312209 Snx6 sorting nexin 6 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20191114 MGI PMID:28134614 1312209 Snx6 sorting nexin 6 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20210506 MGI PMID:29293958 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210506 MGI PMID:32679235 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0001925 male infertility IAGP N RGD:5509061 20210506 MGI PMID:29293958 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0001967 deafness IAGP N RGD:5509061 20210506 MGI PMID:29293958 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210506 MGI PMID:32679235 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210506 MGI PMID:29293958 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20210506 MGI PMID:29293958 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20210506 MGI PMID:29293958 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20210506 MGI PMID:29293958 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0004408 decreased cochlear hair cell number IAGP N RGD:5509061 20210506 MGI PMID:32679235 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20210506 MGI PMID:32679235 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0004528 fused outer hair cell stereocilia IAGP N RGD:5509061 20210506 MGI PMID:29293958 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20210506 MGI PMID:29293958 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20210506 MGI PMID:29293958 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20210506 MGI PMID:29293958 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20210506 MGI PMID:32679235 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210506 MGI PMID:29293958 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210506 MGI PMID:32679235 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0006325 impaired hearing IAGP N RGD:5509061 20210506 MGI PMID:32679235 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20210506 MGI PMID:32679235 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210506 MGI PMID:32679235 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20210506 MGI PMID:32679235 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0009234 absent sperm head IAGP N RGD:5509061 20210506 MGI PMID:32679235 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20210506 MGI PMID:32679235 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0010723 paternal effect IAGP N RGD:5509061 20210506 MGI PMID:32679235 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210506 MGI PMID:29293958 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20210506 MGI PMID:29293958 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20210506 MGI PMID:32679235 1312212 Cdc14a CDC14 cell division cycle 14A gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210506 MGI PMID:32679235 1312215 Ppp1r13b protein phosphatase 1, regulatory subunit 13B gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:18304521 1312215 Ppp1r13b protein phosphatase 1, regulatory subunit 13B gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18304521 1312215 Ppp1r13b protein phosphatase 1, regulatory subunit 13B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15090446 1312215 Ppp1r13b protein phosphatase 1, regulatory subunit 13B gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20141003 MGI PMID:18304521 1312215 Ppp1r13b protein phosphatase 1, regulatory subunit 13B gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18304521 1312219 Mad1l1 MAD1 mitotic arrest deficient 1-like 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17210695 1312219 Mad1l1 MAD1 mitotic arrest deficient 1-like 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17210695 1312219 Mad1l1 MAD1 mitotic arrest deficient 1-like 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17210695 1312219 Mad1l1 MAD1 mitotic arrest deficient 1-like 1 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17210695 1312219 Mad1l1 MAD1 mitotic arrest deficient 1-like 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17210695 1312219 Mad1l1 MAD1 mitotic arrest deficient 1-like 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17210695 1312219 Mad1l1 MAD1 mitotic arrest deficient 1-like 1 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17210695 1312219 Mad1l1 MAD1 mitotic arrest deficient 1-like 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17210695 1312219 Mad1l1 MAD1 mitotic arrest deficient 1-like 1 gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20141003 MGI PMID:17210695 1312219 Mad1l1 MAD1 mitotic arrest deficient 1-like 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:17210695 1312219 Mad1l1 MAD1 mitotic arrest deficient 1-like 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17210695 1312219 Mad1l1 MAD1 mitotic arrest deficient 1-like 1 gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20141003 MGI PMID:17210695 1312219 Mad1l1 MAD1 mitotic arrest deficient 1-like 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17210695 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20201022 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:22915103 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:22915103 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:22915103 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22915103 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22915103 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10224267 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22915103 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0001293 anophthalmia IEA N RGD:5509061 20220519 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0001314 cornea opacity IEA N RGD:5509061 20210128 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20220519 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20210520 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20210128 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20190502 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20210826 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:22915103 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:22915103 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220519 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0010205 abnormal oligodendrocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22915103 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10224267 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15489520 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20190502 MGI 1312225 Tenm4 teneurin transmembrane protein 4 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20180201 MGI PMID:28453519 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20180201 MGI PMID:28453519 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20180201 MGI PMID:28453519 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210520 MGI 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:24270516 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20221215 MGI 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210826 MGI 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20180201 MGI PMID:28453519 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20220811 MGI 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20180201 MGI PMID:28453519 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:24270516 1312227 Arhgef2 Rho/Rac guanine nucleotide exchange factor 2 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:24270516 1312229 Ccl27a C-C motif chemokine ligand 27A gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20240613 MGI PMID:35663027 1312229 Ccl27a C-C motif chemokine ligand 27A gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20240613 MGI PMID:35663027 1312229 Ccl27a C-C motif chemokine ligand 27A gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20240613 MGI PMID:35663027 1312229 Ccl27a C-C motif chemokine ligand 27A gene MP:0009080 uterus inflammation IAGP N RGD:5509061 20240613 MGI PMID:35663027 1312229 Ccl27a C-C motif chemokine ligand 27A gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20240613 MGI PMID:35663027 1312229 Ccl27a C-C motif chemokine ligand 27A gene MP:0012572 increased susceptibility to chemically induced skin inflammation IAGP N RGD:5509061 20240613 MGI PMID:35663027 1312229 Ccl27a C-C motif chemokine ligand 27A gene MP:0020212 impaired leukocyte migration IAGP N RGD:5509061 20240613 MGI PMID:35663027 1312233 Pla2g12a phospholipase A2, group XIIA gene MP:0020099 increased susceptibility to diet-induced aortic fatty streak lesions IAGP N RGD:5509061 20200820 MGI PMID:28917158 1312235 Tnfaip2 tumor necrosis factor, alpha-induced protein 2 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20231221 MGI PMID:33722931 1312235 Tnfaip2 tumor necrosis factor, alpha-induced protein 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20231221 MGI PMID:33722931 1312235 Tnfaip2 tumor necrosis factor, alpha-induced protein 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20231221 MGI PMID:33722931 1312235 Tnfaip2 tumor necrosis factor, alpha-induced protein 2 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20231221 MGI PMID:33722931 1312235 Tnfaip2 tumor necrosis factor, alpha-induced protein 2 gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20231221 MGI PMID:33722931 1312235 Tnfaip2 tumor necrosis factor, alpha-induced protein 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20231221 MGI PMID:33722931 1312235 Tnfaip2 tumor necrosis factor, alpha-induced protein 2 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20231221 MGI PMID:33722931 1312235 Tnfaip2 tumor necrosis factor, alpha-induced protein 2 gene MP:0011282 increased podocyte apoptosis IAGP N RGD:5509061 20231221 MGI PMID:33722931 1312235 Tnfaip2 tumor necrosis factor, alpha-induced protein 2 gene MP:0011293 dilated nephron IAGP N RGD:5509061 20231221 MGI PMID:33722931 1312235 Tnfaip2 tumor necrosis factor, alpha-induced protein 2 gene MP:0011402 renal cast IAGP N RGD:5509061 20231221 MGI PMID:33722931 1312235 Tnfaip2 tumor necrosis factor, alpha-induced protein 2 gene MP:0011498 abnormal glomerular capsule parietal layer morphology IAGP N RGD:5509061 20231221 MGI PMID:33722931 1312235 Tnfaip2 tumor necrosis factor, alpha-induced protein 2 gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20231221 MGI PMID:33722931 1312235 Tnfaip2 tumor necrosis factor, alpha-induced protein 2 gene MP:0011863 abnormal podocyte physiology IAGP N RGD:5509061 20231221 MGI PMID:33722931 1312241 Paip2 polyadenylate-binding protein-interacting protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20739757 1312241 Paip2 polyadenylate-binding protein-interacting protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20739757 1312241 Paip2 polyadenylate-binding protein-interacting protein 2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20739757 1312241 Paip2 polyadenylate-binding protein-interacting protein 2 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:20739757 1312241 Paip2 polyadenylate-binding protein-interacting protein 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:20739757 1312241 Paip2 polyadenylate-binding protein-interacting protein 2 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:20739757 1312241 Paip2 polyadenylate-binding protein-interacting protein 2 gene MP:0004962 decreased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:20739757 1312241 Paip2 polyadenylate-binding protein-interacting protein 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:20739757 1312241 Paip2 polyadenylate-binding protein-interacting protein 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20739757 1312241 Paip2 polyadenylate-binding protein-interacting protein 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:20739757 1312241 Paip2 polyadenylate-binding protein-interacting protein 2 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20141003 MGI PMID:20739757 1312241 Paip2 polyadenylate-binding protein-interacting protein 2 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:20739757 1312241 Paip2 polyadenylate-binding protein-interacting protein 2 gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20141003 MGI PMID:20739757 1312245 Blmh bleomycin hydrolase gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:10200322 1312245 Blmh bleomycin hydrolase gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:10200322 1312245 Blmh bleomycin hydrolase gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:10200322 1312245 Blmh bleomycin hydrolase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10200322 1312245 Blmh bleomycin hydrolase gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:10200322 1312245 Blmh bleomycin hydrolase gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10200322 1312245 Blmh bleomycin hydrolase gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10200322 1312245 Blmh bleomycin hydrolase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10200322 1312247 Ccndbp1 cyclin D-type binding-protein 1 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17256742 1312247 Ccndbp1 cyclin D-type binding-protein 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17256742 1312247 Ccndbp1 cyclin D-type binding-protein 1 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17256742 1312247 Ccndbp1 cyclin D-type binding-protein 1 gene MP:0031324 delayed liver regeneration IAGP N RGD:5509061 20220106 MGI PMID:17256742 1312250 Snapc1 small nuclear RNA activating complex, polypeptide 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 1312250 Snapc1 small nuclear RNA activating complex, polypeptide 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 1312250 Snapc1 small nuclear RNA activating complex, polypeptide 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312250 Snapc1 small nuclear RNA activating complex, polypeptide 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1312250 Snapc1 small nuclear RNA activating complex, polypeptide 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1312253 Oxct1 3-oxoacid CoA transferase 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:21209089 1312253 Oxct1 3-oxoacid CoA transferase 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21209089 1312253 Oxct1 3-oxoacid CoA transferase 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21209089 1312253 Oxct1 3-oxoacid CoA transferase 1 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:21209089 1312253 Oxct1 3-oxoacid CoA transferase 1 gene MP:0003031 acidosis IAGP N RGD:5509061 20141003 MGI PMID:21209089 1312253 Oxct1 3-oxoacid CoA transferase 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:21209089 1312253 Oxct1 3-oxoacid CoA transferase 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:21209089 1312253 Oxct1 3-oxoacid CoA transferase 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21209089 1312253 Oxct1 3-oxoacid CoA transferase 1 gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:21209089 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17658952 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17658952 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11375938 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17658952 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:11375938 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0000447 flattened snout IAGP N RGD:5509061 20171019 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0001142 abnormal vagina orifice morphology IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11375938 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11375938 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170314 MGI PMID:27264173 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20170314 MGI PMID:27264173 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11375938 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0001924 infertility IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0001924 infertility IAGP N RGD:5509061 20170314 MGI PMID:27264173 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0002188 small heart IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:11375938 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20220804 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:11375938 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:11375938 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:11375938 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:17658952 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20220804 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11375938 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:17658952 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20170314 MGI PMID:27264173 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0013599 Leydig cell atrophy IAGP N RGD:5509061 20220804 MGI PMID:18483174 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20160428 MGI PMID:24993042 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0030066 short face IEA N RGD:5509061 20171019 MGI 1312255 Ddr2 discoidin domain receptor family, member 2 gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220804 MGI PMID:18483174 1312256 Plch2 phospholipase C, eta 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20060933 1312258 Tollip toll interacting protein gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16428431 1312258 Tollip toll interacting protein gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:16428431 1312258 Tollip toll interacting protein gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:16428431 1312260 Pank1 pantothenate kinase 1 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20559429 1312260 Pank1 pantothenate kinase 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1312260 Pank1 pantothenate kinase 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:20559429 1312260 Pank1 pantothenate kinase 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20559429 1312260 Pank1 pantothenate kinase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1312260 Pank1 pantothenate kinase 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:20559429 1312260 Pank1 pantothenate kinase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:20559429 1312260 Pank1 pantothenate kinase 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20559429 1312260 Pank1 pantothenate kinase 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:20559429 1312260 Pank1 pantothenate kinase 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:20559429 1312260 Pank1 pantothenate kinase 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20559429 1312260 Pank1 pantothenate kinase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:20559429 1312260 Pank1 pantothenate kinase 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20559429 1312260 Pank1 pantothenate kinase 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20559429 1312260 Pank1 pantothenate kinase 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20559429 1312260 Pank1 pantothenate kinase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22815849 1312260 Pank1 pantothenate kinase 1 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:22815849 1312262 Gdf1 growth differentiation factor 1 gene MP:0000087 absent mandible IAGP N RGD:5509061 20171026 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18615710 1312262 Gdf1 growth differentiation factor 1 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:10700179 1312262 Gdf1 growth differentiation factor 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:10700179 1312262 Gdf1 growth differentiation factor 1 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:10700179 1312262 Gdf1 growth differentiation factor 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:10700179 1312262 Gdf1 growth differentiation factor 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:17936261 1312262 Gdf1 growth differentiation factor 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10700179 1312262 Gdf1 growth differentiation factor 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:10700179 1312262 Gdf1 growth differentiation factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17936261 1312262 Gdf1 growth differentiation factor 1 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:17936261 1312262 Gdf1 growth differentiation factor 1 gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:10700179 1312262 Gdf1 growth differentiation factor 1 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:10700179 1312262 Gdf1 growth differentiation factor 1 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:18615710 1312262 Gdf1 growth differentiation factor 1 gene MP:0004388 absent prechordal plate IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0004714 truncated notochord IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0006062 abnormal vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:10700179 1312262 Gdf1 growth differentiation factor 1 gene MP:0006261 annular pancreas IAGP N RGD:5509061 20141003 MGI PMID:10700179 1312262 Gdf1 growth differentiation factor 1 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17936261 1312262 Gdf1 growth differentiation factor 1 gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0009905 absent tongue IAGP N RGD:5509061 20171026 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0010335 fused first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:10700179 1312262 Gdf1 growth differentiation factor 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:10700179 1312262 Gdf1 growth differentiation factor 1 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:10700179 1312262 Gdf1 growth differentiation factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10700179 1312262 Gdf1 growth differentiation factor 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18615710 1312262 Gdf1 growth differentiation factor 1 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17936261 1312262 Gdf1 growth differentiation factor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10700179 1312262 Gdf1 growth differentiation factor 1 gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20141003 MGI PMID:17936261 1312262 Gdf1 growth differentiation factor 1 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:16564040 1312262 Gdf1 growth differentiation factor 1 gene MP:0012159 absent anterior visceral endoderm IAGP N RGD:5509061 20141003 MGI PMID:17936261 1312262 Gdf1 growth differentiation factor 1 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:17936261 1312262 Gdf1 growth differentiation factor 1 gene MP:0030198 nasal septum hypoplasia IAGP N RGD:5509061 20171012 MGI PMID:16564040 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0001304 cataract IEA N RGD:5509061 20210520 MGI 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0001577 anemia IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0002083 premature death IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20220519 MGI 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:20230755 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0010039 abnormal trophoblast giant cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20230755 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20230755 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20230755 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:20230755 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0013415 increased myeloid cell number in bone marrow IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20150730 MGI PMID:25678499 1312264 Chordc1 cysteine and histidine rich domain containing 1 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:25678499 1312266 Epha1 Eph receptor A1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:18802966 1312266 Epha1 Eph receptor A1 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:18802966 1312266 Epha1 Eph receptor A1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:18802966 1312266 Epha1 Eph receptor A1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18802966 1312266 Epha1 Eph receptor A1 gene MP:0003537 hydrometrocolpos IAGP N RGD:5509061 20141003 MGI PMID:18802966 1312266 Epha1 Eph receptor A1 gene MP:0003541 vaginal inflammation IAGP N RGD:5509061 20141003 MGI PMID:18802966 1312266 Epha1 Eph receptor A1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18802966 1312266 Epha1 Eph receptor A1 gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:18802966 1312266 Epha1 Eph receptor A1 gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:18802966 1312266 Epha1 Eph receptor A1 gene MP:0009087 dilated uterine horn IAGP N RGD:5509061 20141003 MGI PMID:18802966 1312266 Epha1 Eph receptor A1 gene MP:0009360 endometrium inflammation IAGP N RGD:5509061 20141003 MGI PMID:18802966 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11807096 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15381686 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16235133 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:1634998 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17197442 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0000753 paralysis IEA N RGD:5509061 20150312 MGI 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:1634998 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0000755 hindlimb paralysis IEA N RGD:5509061 20150312 MGI 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:15381686 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:17197442 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15381686 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:1634998 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15381686 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0001377 abnormal mating frequency IAGP N RGD:5509061 20141003 MGI PMID:11807096 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11807096 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15381686 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:1634998 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0001410 head bobbing IEA N RGD:5509061 20111116 MGI 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0001504 abnormal posture IEA N RGD:5509061 20111116 MGI 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:11807096 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0001525 impaired balance IEA N RGD:5509061 20111116 MGI 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0001851 eye inflammation IEA N RGD:5509061 20150312 MGI 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:1634998 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0001967 deafness IAGP N RGD:5509061 20150312 MGI PMID:4067076 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20111116 MGI 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15381686 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20141003 MGI PMID:1634998 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0003314 dysmetria IAGP N RGD:5509061 20141003 MGI PMID:15381686 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0003415 priapism IEA N RGD:5509061 20150312 MGI 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0004631 abnormal auditory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11528393 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11528393 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15381686 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0004814 reduced linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:17197442 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11807096 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17197442 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0006325 impaired hearing IEA N RGD:5509061 20111116 MGI 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0009434 paraparesis IEA N RGD:5509061 20111116 MGI 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:11528393 1312270 Sptbn4 spectrin beta, non-erythrocytic 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11528393 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11095744 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16603466 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20190131 MGI PMID:19815523 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16603466 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20160407 MGI PMID:25712131 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20190131 MGI PMID:19815523 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0004213 abnormal umami taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15342734 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:11095744 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0005423 abnormal somatic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15342734 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18367617 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20190314 MGI PMID:19815523 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11095744 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20230713 MGI PMID:12808468 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:18367617 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:23221340 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:11095744 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:11095744 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:23221340 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20160407 MGI PMID:25712131 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:11095744 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:12808468 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:12808468 1312272 Gnat1 G protein subunit alpha transducin 1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:11095744 1312274 Poglut2 protein O-glucosyltransferase 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20240801 MGI PMID:38844137 1312274 Poglut2 protein O-glucosyltransferase 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1312274 Poglut2 protein O-glucosyltransferase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240801 MGI PMID:38844137 1312274 Poglut2 protein O-glucosyltransferase 2 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20240801 MGI PMID:38844137 1312274 Poglut2 protein O-glucosyltransferase 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1312274 Poglut2 protein O-glucosyltransferase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240801 MGI PMID:38844137 1312274 Poglut2 protein O-glucosyltransferase 2 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1312274 Poglut2 protein O-glucosyltransferase 2 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1312274 Poglut2 protein O-glucosyltransferase 2 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1312274 Poglut2 protein O-glucosyltransferase 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20240801 MGI PMID:38844137 1312274 Poglut2 protein O-glucosyltransferase 2 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1312274 Poglut2 protein O-glucosyltransferase 2 gene MP:0006083 abnormal blood vessel elastic tissue morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1312274 Poglut2 protein O-glucosyltransferase 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20240801 MGI PMID:38844137 1312274 Poglut2 protein O-glucosyltransferase 2 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1312274 Poglut2 protein O-glucosyltransferase 2 gene MP:0031392 hypoactivity IAGP N RGD:5509061 20240801 MGI PMID:38844137 1312277 Eif1ad eukaryotic translation initiation factor 1A domain containing gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1312277 Eif1ad eukaryotic translation initiation factor 1A domain containing gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312277 Eif1ad eukaryotic translation initiation factor 1A domain containing gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 1312277 Eif1ad eukaryotic translation initiation factor 1A domain containing gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1312277 Eif1ad eukaryotic translation initiation factor 1A domain containing gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1312278 Alkbh8 alkB homolog 8, tRNA methyltransferase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1312278 Alkbh8 alkB homolog 8, tRNA methyltransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20123966 1312278 Alkbh8 alkB homolog 8, tRNA methyltransferase gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1312278 Alkbh8 alkB homolog 8, tRNA methyltransferase gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1312278 Alkbh8 alkB homolog 8, tRNA methyltransferase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1312282 Eml4 echinoderm microtubule associated protein like 4 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1312282 Eml4 echinoderm microtubule associated protein like 4 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1312282 Eml4 echinoderm microtubule associated protein like 4 gene MP:0003896 prolonged PR interval IEA N RGD:5509061 20240523 MGI 1312282 Eml4 echinoderm microtubule associated protein like 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0000692 small spleen IEA N RGD:5509061 20200514 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0001259 abnormal body weight IEA N RGD:5509061 20240523 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20200514 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20200514 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20240523 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20220811 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210826 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200514 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210826 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 1312284 Rabgap1 RAB GTPase activating protein 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1312288 5031439G07Rik RIKEN cDNA 5031439G07 gene gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1312293 Actl7a actin-like 7a gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20211209 MGI PMID:32923619 1312293 Actl7a actin-like 7a gene MP:0001925 male infertility IAGP N RGD:5509061 20211209 MGI PMID:32923619 1312293 Actl7a actin-like 7a gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20211209 MGI PMID:32923619 1312293 Actl7a actin-like 7a gene MP:0009231 detached acrosome IAGP N RGD:5509061 20211209 MGI PMID:32923619 1312296 Naxe NAD(P)HX epimerase gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210128 MGI 1312296 Naxe NAD(P)HX epimerase gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20190228 MGI PMID:28325782 1312296 Naxe NAD(P)HX epimerase gene MP:0003711 pathological neovascularization IAGP N RGD:5509061 20190228 MGI PMID:28325782 1312296 Naxe NAD(P)HX epimerase gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20190228 MGI PMID:28325782 1312298 Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:10466727 1312298 Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10466727 1312298 Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 gene MP:0000361 decreased mast cell protease storage IAGP N RGD:5509061 20141003 MGI PMID:10466726 1312298 Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 gene MP:0000361 decreased mast cell protease storage IAGP N RGD:5509061 20141003 MGI PMID:10466727 1312298 Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 gene MP:0000362 decreased mast cell histamine storage IAGP N RGD:5509061 20141003 MGI PMID:10466726 1312298 Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 gene MP:0000362 decreased mast cell histamine storage IAGP N RGD:5509061 20141003 MGI PMID:10466727 1312298 Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20141003 MGI PMID:18077586 1312298 Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20141003 MGI PMID:22745308 1312298 Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:19109198 1312298 Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:10466726 1312298 Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 gene MP:0005462 abnormal mast cell differentiation IAGP N RGD:5509061 20150416 MGI PMID:19109198 1312298 Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:10466726 1312298 Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:10466727 1312298 Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16056228 1312298 Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 gene MP:0013331 abnormal lacrimal gland development IAGP N RGD:5509061 20141204 MGI PMID:22745308 1312304 Tnfrsf17 tumor necrosis factor receptor superfamily, member 17 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11509691 1312304 Tnfrsf17 tumor necrosis factor receptor superfamily, member 17 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210128 MGI 1312304 Tnfrsf17 tumor necrosis factor receptor superfamily, member 17 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:14707116 1312304 Tnfrsf17 tumor necrosis factor receptor superfamily, member 17 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210826 MGI 1312306 Rtraf RNA transcription, translation and transport factor gene MP:0000745 tremors IEA N RGD:5509061 20170105 MGI 1312306 Rtraf RNA transcription, translation and transport factor gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1312306 Rtraf RNA transcription, translation and transport factor gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20210128 MGI 1312306 Rtraf RNA transcription, translation and transport factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312306 Rtraf RNA transcription, translation and transport factor gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1312308 Tmem147 transmembrane protein 147 gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20210826 MGI 1312308 Tmem147 transmembrane protein 147 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20210826 MGI 1312308 Tmem147 transmembrane protein 147 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312314 Car8 carbonic anhydrase 8 gene MP:0000745 tremors IAGP N RGD:5509061 20160519 MGI PMID:26586559 1312314 Car8 carbonic anhydrase 8 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20160519 MGI PMID:26586559 1312314 Car8 carbonic anhydrase 8 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20160519 MGI PMID:26586559 1312314 Car8 carbonic anhydrase 8 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16118194 1312314 Car8 carbonic anhydrase 8 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160519 MGI PMID:26586559 1312314 Car8 carbonic anhydrase 8 gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 1312314 Car8 carbonic anhydrase 8 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20160519 MGI PMID:26586559 1312314 Car8 carbonic anhydrase 8 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20160519 MGI PMID:26586559 1312314 Car8 carbonic anhydrase 8 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20141003 MGI 1312314 Car8 carbonic anhydrase 8 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20160519 MGI PMID:26586559 1312319 Jcad junctional cadherin 5 associated gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191031 MGI PMID:28705794 1312319 Jcad junctional cadherin 5 associated gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1312319 Jcad junctional cadherin 5 associated gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230601 MGI 1312319 Jcad junctional cadherin 5 associated gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20191031 MGI PMID:28705794 1312319 Jcad junctional cadherin 5 associated gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210520 MGI 1312319 Jcad junctional cadherin 5 associated gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20191031 MGI PMID:28705794 1312319 Jcad junctional cadherin 5 associated gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20191031 MGI PMID:28705794 1312319 Jcad junctional cadherin 5 associated gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1312319 Jcad junctional cadherin 5 associated gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1312321 Eral1 Era like 12S mitochondrial rRNA chaperone 1 gene MP:0003896 prolonged PR interval IEA N RGD:5509061 20221215 MGI 1312321 Eral1 Era like 12S mitochondrial rRNA chaperone 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312321 Eral1 Era like 12S mitochondrial rRNA chaperone 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1312325 Cxcl17 C-X-C motif chemokine ligand 17 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1312325 Cxcl17 C-X-C motif chemokine ligand 17 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1312325 Cxcl17 C-X-C motif chemokine ligand 17 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1312325 Cxcl17 C-X-C motif chemokine ligand 17 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20170105 MGI 1312325 Cxcl17 C-X-C motif chemokine ligand 17 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201231 MGI 1312325 Cxcl17 C-X-C motif chemokine ligand 17 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1312325 Cxcl17 C-X-C motif chemokine ligand 17 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1312325 Cxcl17 C-X-C motif chemokine ligand 17 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1312325 Cxcl17 C-X-C motif chemokine ligand 17 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210520 MGI 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20201029 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20201029 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20201029 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20201029 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20201029 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20201029 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20201029 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20201029 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20201022 MGI PMID:26062998 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20201029 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20201029 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20201029 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20201022 MGI PMID:26062998 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0008141 decreased small intestinal microvillus size IAGP N RGD:5509061 20201029 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20201029 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20201029 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20201029 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0014262 increased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:31296356 1312329 Ikzf4 IKAROS family zinc finger 4 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1312332 Cadm4 cell adhesion molecule 4 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:23825401 1312332 Cadm4 cell adhesion molecule 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23825401 1312332 Cadm4 cell adhesion molecule 4 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:23825401 1312332 Cadm4 cell adhesion molecule 4 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:23825401 1312332 Cadm4 cell adhesion molecule 4 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:23825401 1312332 Cadm4 cell adhesion molecule 4 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:23825401 1312332 Cadm4 cell adhesion molecule 4 gene MP:0010734 abnormal paranode morphology IAGP N RGD:5509061 20141003 MGI PMID:23825401 1312333 Them4 thioesterase superfamily member 4 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:19421406 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230119 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20230119 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20231207 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:19470461 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0000601 small liver IEA N RGD:5509061 20230119 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:19470461 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19470461 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20231207 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20230119 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230119 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230119 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230119 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:19470461 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20141003 MGI PMID:19470461 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20231207 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20230119 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20231207 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20231207 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 1312335 Sox21 SRY (sex determining region Y)-box 21 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 1312337 Dnajb1 DnaJ heat shock protein family (Hsp40) member B1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17050614 1312340 4933427D14Rik RIKEN cDNA 4933427D14 gene gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191128 MGI 1312340 4933427D14Rik RIKEN cDNA 4933427D14 gene gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20191128 MGI 1312340 4933427D14Rik RIKEN cDNA 4933427D14 gene gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20191128 MGI 1312340 4933427D14Rik RIKEN cDNA 4933427D14 gene gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240620 MGI 1312342 Sfn stratifin gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17041603 1312342 Sfn stratifin gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:24075906 1312342 Sfn stratifin gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20439433 1312342 Sfn stratifin gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0000384 distorted hair follicle pattern IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0000416 sparse hair IEA N RGD:5509061 20111116 MGI 1312342 Sfn stratifin gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0000447 flattened snout IAGP N RGD:5509061 20141003 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20141003 MGI PMID:17041603 1312342 Sfn stratifin gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:16239341 1312342 Sfn stratifin gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:17041603 1312342 Sfn stratifin gene MP:0000564 syndactyly IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:17041603 1312342 Sfn stratifin gene MP:0000585 kinked tail IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:16239341 1312342 Sfn stratifin gene MP:0000592 short tail IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:21205887 1312342 Sfn stratifin gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:16239341 1312342 Sfn stratifin gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:6174530 1312342 Sfn stratifin gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17041603 1312342 Sfn stratifin gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:6174530 1312342 Sfn stratifin gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0001218 thin epidermis IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:16239341 1312342 Sfn stratifin gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:17041603 1312342 Sfn stratifin gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:24075906 1312342 Sfn stratifin gene MP:0001219 thick epidermis IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16239341 1312342 Sfn stratifin gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:6174530 1312342 Sfn stratifin gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17041603 1312342 Sfn stratifin gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:6174530 1312342 Sfn stratifin gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:24075906 1312342 Sfn stratifin gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:6174530 1312342 Sfn stratifin gene MP:0001241 absent epidermis stratum corneum IAGP N RGD:5509061 20141003 MGI PMID:16239341 1312342 Sfn stratifin gene MP:0001241 absent epidermis stratum corneum IAGP N RGD:5509061 20141003 MGI PMID:17041603 1312342 Sfn stratifin gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0001297 microphthalmia IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:6374282 1312342 Sfn stratifin gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:21205887 1312342 Sfn stratifin gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21205887 1312342 Sfn stratifin gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16239341 1312342 Sfn stratifin gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:2989601 1312342 Sfn stratifin gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:17041603 1312342 Sfn stratifin gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21205887 1312342 Sfn stratifin gene MP:0002234 abnormal pharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0002251 abnormal nasopharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:16239341 1312342 Sfn stratifin gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:24075906 1312342 Sfn stratifin gene MP:0003130 anal atresia IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0003160 abnormal esophagus development IAGP N RGD:5509061 20141003 MGI PMID:17041603 1312342 Sfn stratifin gene MP:0003315 abnormal perineum morphology IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0003385 abnormal body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:17041603 1312342 Sfn stratifin gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:20439433 1312342 Sfn stratifin gene MP:0003671 abnormal eyelid aperture IAGP N RGD:5509061 20141003 MGI PMID:6374282 1312342 Sfn stratifin gene MP:0003775 thin lip IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:2989601 1312342 Sfn stratifin gene MP:0004575 small limb buds IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0004576 abnormal embryonic autopod plate morphology IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21205887 1312342 Sfn stratifin gene MP:0005114 premature hair loss IAGP N RGD:5509061 20141003 MGI PMID:16239341 1312342 Sfn stratifin gene MP:0005114 premature hair loss IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21205887 1312342 Sfn stratifin gene MP:0005155 herniated intestine IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0006033 abnormal external auditory canal morphology IAGP N RGD:5509061 20141003 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:21205887 1312342 Sfn stratifin gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21205887 1312342 Sfn stratifin gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21205887 1312342 Sfn stratifin gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:21205887 1312342 Sfn stratifin gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:21205887 1312342 Sfn stratifin gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21205887 1312342 Sfn stratifin gene MP:0009263 abnormal eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:6374282 1312342 Sfn stratifin gene MP:0009474 thick epidermis stratum spinosum IAGP N RGD:5509061 20141003 MGI PMID:17041603 1312342 Sfn stratifin gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:20439433 1312342 Sfn stratifin gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20439433 1312342 Sfn stratifin gene MP:0009553 fused lips IAGP N RGD:5509061 20141003 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0009553 fused lips IAGP N RGD:5509061 20230601 MGI PMID:6746880 1312342 Sfn stratifin gene MP:0009560 absent epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:16239341 1312342 Sfn stratifin gene MP:0009560 absent epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:17041603 1312342 Sfn stratifin gene MP:0009576 oral atresia IAGP N RGD:5509061 20141003 MGI PMID:24075906 1312342 Sfn stratifin gene MP:0009576 oral atresia IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0009884 palatal shelf fusion with tongue or mandible IAGP N RGD:5509061 20141003 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:479550 1312342 Sfn stratifin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16239341 1312342 Sfn stratifin gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24075906 1312342 Sfn stratifin gene MP:0012175 flat face IAGP N RGD:5509061 20171019 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0013789 small external nares IAGP N RGD:5509061 20150611 MGI PMID:479550 1312342 Sfn stratifin gene MP:0013789 small external nares IAGP N RGD:5509061 20150611 MGI PMID:6643653 1312342 Sfn stratifin gene MP:0013818 abnormal oral cavity morphology IAGP N RGD:5509061 20170914 MGI PMID:479550 1312342 Sfn stratifin gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:21205887 1312342 Sfn stratifin gene MP:0021208 median cleft palate IAGP N RGD:5509061 20221201 MGI PMID:479550 1312342 Sfn stratifin gene MP:0030179 abnormal oral epithelium morphology IAGP N RGD:5509061 20171005 MGI PMID:16239341 1312342 Sfn stratifin gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:21205887 1312346 Styx serine/threonine/tyrosine interaction protein gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11842224 1312346 Styx serine/threonine/tyrosine interaction protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11842224 1312346 Styx serine/threonine/tyrosine interaction protein gene MP:0002208 abnormal germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11842224 1312346 Styx serine/threonine/tyrosine interaction protein gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11842224 1312346 Styx serine/threonine/tyrosine interaction protein gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11842224 1312346 Styx serine/threonine/tyrosine interaction protein gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11842224 1312346 Styx serine/threonine/tyrosine interaction protein gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:11842224 1312349 Elmo3 engulfment and cell motility 3 gene MP:0001314 cornea opacity IEA N RGD:5509061 20170105 MGI 1312349 Elmo3 engulfment and cell motility 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20534472 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:20547853 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:20547853 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20534472 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20547853 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:20534472 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:20547853 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:20534472 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:20547853 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:20534472 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:20547853 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:20534472 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:20547853 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20547853 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:20547853 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:20534472 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:20547853 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:20534472 1312350 Mov10l1 Mov10 like RISC complex RNA helicase 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:20547853 1312354 Zfr2 zinc finger RNA binding protein 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1312356 Ube4b ubiquitination factor E4B gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240627 MGI PMID:36440598 1312356 Ube4b ubiquitination factor E4B gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20240627 MGI PMID:36440598 1312356 Ube4b ubiquitination factor E4B gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20240627 MGI PMID:36440598 1312356 Ube4b ubiquitination factor E4B gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20240627 MGI PMID:36440598 1312356 Ube4b ubiquitination factor E4B gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16314518 1312356 Ube4b ubiquitination factor E4B gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20240627 MGI PMID:36440598 1312356 Ube4b ubiquitination factor E4B gene MP:0021090 abnormal dendrite arborization pattern IAGP N RGD:5509061 20240627 MGI PMID:36440598 1312358 Exosc3 exosome component 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1312358 Exosc3 exosome component 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1312358 Exosc3 exosome component 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1312358 Exosc3 exosome component 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 1312358 Exosc3 exosome component 3 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210128 MGI 1312358 Exosc3 exosome component 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1312358 Exosc3 exosome component 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1312358 Exosc3 exosome component 3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220519 MGI 1312358 Exosc3 exosome component 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1312358 Exosc3 exosome component 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220519 MGI 1312362 Rab37 RAB37, member RAS oncogene family gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20230406 MGI PMID:36109708 1312362 Rab37 RAB37, member RAS oncogene family gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20230406 MGI PMID:36109708 1312366 Stx11 syntaxin 11 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1312366 Stx11 syntaxin 11 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1312366 Stx11 syntaxin 11 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1312366 Stx11 syntaxin 11 gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:23042080 1312366 Stx11 syntaxin 11 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:23042080 1312366 Stx11 syntaxin 11 gene MP:0002833 increased heart weight IEA N RGD:5509061 20201022 MGI 1312366 Stx11 syntaxin 11 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1312366 Stx11 syntaxin 11 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:23042080 1312366 Stx11 syntaxin 11 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23042080 1312366 Stx11 syntaxin 11 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1312366 Stx11 syntaxin 11 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:23042080 1312366 Stx11 syntaxin 11 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210520 MGI 1312366 Stx11 syntaxin 11 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23042080 1312366 Stx11 syntaxin 11 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23042080 1312366 Stx11 syntaxin 11 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0008791 decreased NK cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1312366 Stx11 syntaxin 11 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1312366 Stx11 syntaxin 11 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:23160464 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20220519 MGI PMID:34420035 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20220519 MGI PMID:34420035 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:11274056 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:11274056 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20220519 MGI PMID:34420035 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20220519 MGI PMID:34420035 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20220519 MGI PMID:34420035 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11274056 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12730693 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:11242117 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11242117 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12730693 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20220519 MGI PMID:34420035 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20220519 MGI PMID:34420035 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:12730693 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0004031 insulitis IAGP N RGD:5509061 20220519 MGI PMID:34420035 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20220519 MGI PMID:34420035 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20220519 MGI PMID:34420035 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20220519 MGI PMID:34420035 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20220519 MGI PMID:34420035 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20220519 MGI PMID:34420035 1312369 Mbd2 methyl-CpG binding domain protein 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11274056 1312371 Adcy9 adenylate cyclase 9 gene MP:0000497 abnormal small intestine placement IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20190221 MGI PMID:28717248 1312371 Adcy9 adenylate cyclase 9 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1312371 Adcy9 adenylate cyclase 9 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20211021 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0003888 liver hemorrhage IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0004666 absent stapedial artery IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0005272 abnormal temporal bone morphology IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20190221 MGI PMID:28717248 1312371 Adcy9 adenylate cyclase 9 gene MP:0008499 increased IgG1 level IEA N RGD:5509061 20111116 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0009571 abnormal right lung accessory lobe morphology IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20190221 MGI PMID:28717248 1312371 Adcy9 adenylate cyclase 9 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1312371 Adcy9 adenylate cyclase 9 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0013847 retropleural edema IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0013852 abnormal Mullerian duct topology IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0013985 abnormal umbilical vein topology IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0014003 additional anastomosis between intracranial vertebral arteries IEA N RGD:5509061 20170504 MGI 1312371 Adcy9 adenylate cyclase 9 gene MP:0014087 retrolental blood IEA N RGD:5509061 20180628 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15469977 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15537447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:15469977 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:21237142 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:21237142 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000107 abnormal frontal bone morphology IEA N RGD:5509061 20111116 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21237142 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000116 abnormal tooth development IEA N RGD:5509061 20111116 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000119 abnormal tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:5893447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000128 growth retardation of molars IEA N RGD:5509061 20111116 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15469977 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000138 absent vertebrae IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:15469977 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20151119 MGI PMID:24506864 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:5893447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:21237142 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:21228006 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000436 abnormal head movements IEA N RGD:5509061 20111116 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15537447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:15537447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15537447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000555 absent carpal bone IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:15537447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:15469977 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000566 synostosis IAGP N RGD:5509061 20141003 MGI PMID:15537447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:10545599 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:15384171 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:16126904 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:21228006 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:24203697 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:15469977 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:22232553 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20151119 MGI PMID:25917329 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20151119 MGI PMID:24506864 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:22232553 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:21228006 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21228006 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:21228006 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10545599 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15384171 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16126904 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:23968836 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:15469977 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22232553 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10545599 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001293 anophthalmia IEA N RGD:5509061 20111116 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:5893447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20111116 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20151119 MGI PMID:24506864 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20151119 MGI PMID:24506864 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001677 absent apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16126904 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:15469977 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15384171 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001732 postnatal growth retardation IEA N RGD:5509061 20111116 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20151119 MGI PMID:25917329 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16126904 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:15537447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18948618 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20151119 MGI PMID:24506864 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002177 abnormal outer ear morphology IEA N RGD:5509061 20111116 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002233 abnormal nose morphology IEA N RGD:5509061 20111116 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20151119 MGI PMID:24506864 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20151119 MGI PMID:25917329 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002632 vestigial tail IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19718039 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:19718039 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16126904 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002861 abnormal tail bud morphology IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:22232553 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:22232553 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:19718039 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16126904 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003050 abnormal sacral vertebrae morphology IEA N RGD:5509061 20111116 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:15469977 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:24203697 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:23968836 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:24203697 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003074 absent metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003126 abnormal external female genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:15384171 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20151119 MGI PMID:25917329 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003445 sirenomelia IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003445 sirenomelia IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:19718039 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:23968836 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003800 monodactyly IAGP N RGD:5509061 20141003 MGI PMID:15537447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20151119 MGI PMID:24506864 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20151119 MGI PMID:24506864 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:15537447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:21228006 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:24203697 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15469977 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:16126904 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:16126904 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0004652 small caudal vertebrae IEA N RGD:5509061 20111116 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0004830 short incisors IEA N RGD:5509061 20171005 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15537447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:21237142 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:15469977 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:16126904 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20151119 MGI PMID:24506864 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22232553 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:15469977 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20151119 MGI PMID:24506864 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20151119 MGI PMID:24506864 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20151119 MGI PMID:24506864 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005352 small cranium IEA N RGD:5509061 20111116 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005430 absent fibula IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:19718039 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22232553 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22232553 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0006400 decreased molar number IAGP N RGD:5509061 20141003 MGI PMID:5893447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0006402 small molars IAGP N RGD:5509061 20141003 MGI PMID:5893447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15469977 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0008274 failure of bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:21237142 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:23968836 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0008832 hemivertebra IAGP N RGD:5509061 20141003 MGI PMID:16126904 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0009039 absent inferior colliculus IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0009127 increased brown fat cell number IAGP N RGD:5509061 20141003 MGI PMID:22232553 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0009199 abnormal external male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20151119 MGI PMID:24506864 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22232553 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0009703 decreased birth body size IEA N RGD:5509061 20111116 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20151119 MGI PMID:24506864 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20151119 MGI PMID:25917329 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0010715 retina coloboma IAGP N RGD:5509061 20141003 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0010743 delayed cranial suture closure IEA N RGD:5509061 20111116 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15469977 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21924256 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10545599 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21237142 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10545599 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20111201 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0011496 abnormal head size IAGP N RGD:5509061 20141003 MGI PMID:21228006 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:16126904 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0012062 small tail bud IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0012078 abnormal tail ring morphology IAGP N RGD:5509061 20170309 MGI PMID:5893447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0012139 increased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0012184 absent paraxial mesoderm IAGP N RGD:5509061 20141003 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0012547 spina bifida cystica IAGP N RGD:5509061 20141003 MGI PMID:15469977 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0013207 absent endoderm IAGP N RGD:5509061 20141003 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:21237142 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:11029008 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:15142971 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:15537447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:19653321 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20180125 MGI PMID:22232553 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0030080 small lower incisors IAGP N RGD:5509061 20170928 MGI PMID:5893447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0030083 long upper incisors IEA N RGD:5509061 20180125 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0030279 thin neurocranium IEA N RGD:5509061 20171102 MGI 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20171221 MGI PMID:5893447 1312374 Lrp6 low density lipoprotein receptor-related protein 6 gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:22232553 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:19014927 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0001147 small testis IAGP N RGD:5509061 20150917 MGI PMID:18339773 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20150917 MGI PMID:18339773 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19014927 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20150917 MGI PMID:18339773 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18753606 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19014927 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:19014927 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:19014927 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:19014927 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20150917 MGI PMID:18339773 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0003357 impaired granulosa cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18753606 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:18753606 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:19014927 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20150917 MGI PMID:18339773 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20150917 MGI PMID:18339773 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:18753606 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:19014927 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20150917 MGI PMID:18339773 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19014927 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20150917 MGI PMID:18339773 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:18753606 1312378 Sohlh2 spermatogenesis and oogenesis specific basic helix-loop-helix 2 gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:18753606 1312381 Hcls1 hematopoietic cell specific Lyn substrate 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1312381 Hcls1 hematopoietic cell specific Lyn substrate 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 1312381 Hcls1 hematopoietic cell specific Lyn substrate 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 1312381 Hcls1 hematopoietic cell specific Lyn substrate 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 1312381 Hcls1 hematopoietic cell specific Lyn substrate 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20240523 MGI 1312381 Hcls1 hematopoietic cell specific Lyn substrate 1 gene MP:0001147 small testis IEA N RGD:5509061 20240523 MGI 1312381 Hcls1 hematopoietic cell specific Lyn substrate 1 gene MP:0001333 absent optic nerve IEA N RGD:5509061 20240523 MGI 1312381 Hcls1 hematopoietic cell specific Lyn substrate 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:7641686 1312381 Hcls1 hematopoietic cell specific Lyn substrate 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 1312381 Hcls1 hematopoietic cell specific Lyn substrate 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7641686 1312381 Hcls1 hematopoietic cell specific Lyn substrate 1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20240523 MGI 1312381 Hcls1 hematopoietic cell specific Lyn substrate 1 gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:7641686 1312381 Hcls1 hematopoietic cell specific Lyn substrate 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:7641686 1312381 Hcls1 hematopoietic cell specific Lyn substrate 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:7641686 1312381 Hcls1 hematopoietic cell specific Lyn substrate 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7641686 1312383 Phlda2 pleckstrin homology like domain, family A, member 2 gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:12032310 1312383 Phlda2 pleckstrin homology like domain, family A, member 2 gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:12032310 1312383 Phlda2 pleckstrin homology like domain, family A, member 2 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:12032310 1312383 Phlda2 pleckstrin homology like domain, family A, member 2 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:12032310 1312383 Phlda2 pleckstrin homology like domain, family A, member 2 gene MP:0012098 increased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:12032310 1312383 Phlda2 pleckstrin homology like domain, family A, member 2 gene MP:0012108 increased trophoblast glycogen cell number IAGP N RGD:5509061 20141003 MGI PMID:12032310 1312385 Fank1 fibronectin type 3 and ankyrin repeat domains 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:31086747 1312388 Palb2 partner and localizer of BRCA2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:23657012 1312388 Palb2 partner and localizer of BRCA2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:23657012 1312388 Palb2 partner and localizer of BRCA2 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:20484223 1312388 Palb2 partner and localizer of BRCA2 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:20484223 1312388 Palb2 partner and localizer of BRCA2 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:20484223 1312388 Palb2 partner and localizer of BRCA2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20484223 1312388 Palb2 partner and localizer of BRCA2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23657012 1312388 Palb2 partner and localizer of BRCA2 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1312388 Palb2 partner and localizer of BRCA2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:20484223 1312388 Palb2 partner and localizer of BRCA2 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20211021 MGI 1312388 Palb2 partner and localizer of BRCA2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:20484223 1312388 Palb2 partner and localizer of BRCA2 gene MP:0002861 abnormal tail bud morphology IAGP N RGD:5509061 20141003 MGI PMID:20484223 1312388 Palb2 partner and localizer of BRCA2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23657012 1312388 Palb2 partner and localizer of BRCA2 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:23657012 1312388 Palb2 partner and localizer of BRCA2 gene MP:0003750 increased mouth tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23657012 1312388 Palb2 partner and localizer of BRCA2 gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:20484223 1312388 Palb2 partner and localizer of BRCA2 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:23657012 1312388 Palb2 partner and localizer of BRCA2 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23657012 1312388 Palb2 partner and localizer of BRCA2 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:20484223 1312388 Palb2 partner and localizer of BRCA2 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:20484223 1312388 Palb2 partner and localizer of BRCA2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23657012 1312388 Palb2 partner and localizer of BRCA2 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23657012 1312388 Palb2 partner and localizer of BRCA2 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23657012 1312388 Palb2 partner and localizer of BRCA2 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:23657012 1312388 Palb2 partner and localizer of BRCA2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20484223 1312388 Palb2 partner and localizer of BRCA2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23657012 1312388 Palb2 partner and localizer of BRCA2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23657012 1312388 Palb2 partner and localizer of BRCA2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312388 Palb2 partner and localizer of BRCA2 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23657012 1312388 Palb2 partner and localizer of BRCA2 gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20484223 1312388 Palb2 partner and localizer of BRCA2 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:20484223 1312388 Palb2 partner and localizer of BRCA2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1312399 Ano6 anoctamin 6 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1312399 Ano6 anoctamin 6 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23021219 1312399 Ano6 anoctamin 6 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20201022 MGI 1312399 Ano6 anoctamin 6 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:23021219 1312399 Ano6 anoctamin 6 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:23021219 1312399 Ano6 anoctamin 6 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20180503 MGI PMID:24974903 1312399 Ano6 anoctamin 6 gene MP:0009445 osteomalacia IAGP N RGD:5509061 20141003 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0010926 increased osteoid volume IAGP N RGD:5509061 20141003 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0010929 increased osteoid thickness IAGP N RGD:5509061 20141003 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 1312399 Ano6 anoctamin 6 gene MP:0011954 shortened PQ interval IEA N RGD:5509061 20210826 MGI 1312399 Ano6 anoctamin 6 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0020138 delayed bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0030857 absent olecranon IAGP N RGD:5509061 20181025 MGI PMID:22936354 1312399 Ano6 anoctamin 6 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:23021219 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0000624 xerostomia IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:20660351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:20660351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0001337 dry eyes IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20660351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20660351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002360 abnormal spleen B cell corona morphology IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:20660351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002742 enlarged submandibular lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:19155511 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0003746 stomatitis IAGP N RGD:5509061 20170907 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:19155511 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:19155511 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008121 increased myeloid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:15485634 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008188 abnormal transitional stage B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008524 increased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008542 enlarged cervical lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:19155511 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:19155511 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:19155511 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:23123062 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008879 submandibular gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0008896 increased IgG2c level IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0009521 increased submandibular gland size IAGP N RGD:5509061 20141003 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0010072 increased pruritus IAGP N RGD:5509061 20141003 MGI PMID:20660351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0013367 parotid gland inflammation IAGP N RGD:5509061 20141225 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0013558 abnormal exocrine gland morphology IAGP N RGD:5509061 20170907 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:18624351 1312404 Traf3ip2 TRAF3 interacting protein 2 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:22585710 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20150101 MGI PMID:24550297 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20150101 MGI PMID:24550297 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20150101 MGI PMID:24550297 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20150101 MGI PMID:24550297 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20371351 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20180503 MGI PMID:29438013 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0000601 small liver IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:20371351 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20371351 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20180503 MGI PMID:29438013 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0002083 premature death IAGP N RGD:5509061 20180503 MGI PMID:29438013 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20150101 MGI PMID:24550297 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:20371351 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20230601 MGI 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:20371351 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20180503 MGI PMID:29438013 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20150101 MGI PMID:24550297 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20371351 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20180503 MGI PMID:29438013 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0003824 decreased left ventricle developed pressure IAGP N RGD:5509061 20141003 MGI PMID:20371351 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20180503 MGI PMID:29438013 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20150101 MGI PMID:24550297 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20150101 MGI PMID:24550297 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20371351 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20180503 MGI PMID:29438013 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20180503 MGI PMID:29438013 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20160407 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20180503 MGI PMID:29438013 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20150101 MGI PMID:24550297 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0009198 abnormal male genitalia morphology IEA N RGD:5509061 20230601 MGI 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0009204 absent external male genitalia IEA N RGD:5509061 20230601 MGI 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20150101 MGI PMID:24550297 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0009709 hydrometra IEA N RGD:5509061 20230601 MGI 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230601 MGI 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:20371351 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20180503 MGI PMID:29438013 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20150101 MGI PMID:24550297 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20150101 MGI PMID:24550297 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20371351 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20150101 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20160407 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20190711 MGI PMID:29438013 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:21897366 1312408 Cnot3 CCR4-NOT transcription complex, subunit 3 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:20371351 1312411 Castor1 cytosolic arginine sensor for mTORC1 subunit 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16708114 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19843512 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:19843512 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16708114 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:19843512 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19843512 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19843512 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:19843512 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0004093 diffuse Z line IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19843512 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19843512 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:16708114 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0010393 shortened QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:19843512 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0010554 shortened HV interval IAGP N RGD:5509061 20141003 MGI PMID:19843512 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0020345 abnormal myocardial fiber currents IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0020346 abnormal myocardial fiber calcium currents IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0020347 abnormal myocardial fiber sodium currents IAGP N RGD:5509061 20170824 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0030566 abnormal A band morphology IAGP N RGD:5509061 20180531 MGI PMID:17766470 1312414 Xirp1 xin actin-binding repeat containing 1 gene MP:0030567 abnormal I band morphology IAGP N RGD:5509061 20180531 MGI PMID:17766470 1312419 Lrrc23 leucine rich repeat containing 23 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220310 MGI PMID:34585727 1312419 Lrrc23 leucine rich repeat containing 23 gene MP:0001925 male infertility IAGP N RGD:5509061 20220310 MGI PMID:34585727 1312419 Lrrc23 leucine rich repeat containing 23 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220310 MGI PMID:34585727 1312419 Lrrc23 leucine rich repeat containing 23 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1312419 Lrrc23 leucine rich repeat containing 23 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220310 MGI PMID:34585727 1312419 Lrrc23 leucine rich repeat containing 23 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220310 MGI PMID:34585727 1312419 Lrrc23 leucine rich repeat containing 23 gene MP:0031438 abnormal sperm radial spoke morphology IAGP N RGD:5509061 20220915 MGI PMID:34585727 1312421 Spats2 spermatogenesis associated, serine-rich 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230119 MGI 1312421 Spats2 spermatogenesis associated, serine-rich 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1312423 Trit1 tRNA isopentenyltransferase 1 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1312423 Trit1 tRNA isopentenyltransferase 1 gene MP:0009331 absent primitive node IEA N RGD:5509061 20240627 MGI 1312423 Trit1 tRNA isopentenyltransferase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 1312423 Trit1 tRNA isopentenyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312423 Trit1 tRNA isopentenyltransferase 1 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IEA N RGD:5509061 20241017 MGI 1312423 Trit1 tRNA isopentenyltransferase 1 gene MP:0012724 absent head fold IEA N RGD:5509061 20240627 MGI 1312423 Trit1 tRNA isopentenyltransferase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1312423 Trit1 tRNA isopentenyltransferase 1 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241017 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000035 abnormal membranous labyrinth morphology IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:1638738 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000566 synostosis IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000585 kinked tail IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:10444330 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:17019651 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000774 decreased brain size IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:1638738 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000828 abnormal fourth ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19741143 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:1638738 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:19741143 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17019651 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19741143 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:1638738 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:19741143 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:1638738 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:17019651 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000869 abnormal cerebellum posterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:17019651 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000923 abnormal roof plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000923 abnormal roof plate morphology IAGP N RGD:5509061 20141003 MGI PMID:14251482 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10444330 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10444330 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17019651 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10444330 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:14914015 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001395 bidirectional circling IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10444330 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:14914015 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17019651 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150827 MGI PMID:25915474 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10444330 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001891 hydrocephaly IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001924 infertility IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10444330 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10444330 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:10444330 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:14914015 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:14251482 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0002161 abnormal fertility/fecundity IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20150827 MGI PMID:25915474 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20150827 MGI PMID:25915474 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0002428 abnormal semicircular canal morphology IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0002671 belted IAGP N RGD:5509061 20141003 MGI PMID:10444330 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0002671 belted IAGP N RGD:5509061 20141003 MGI PMID:14914015 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0002862 abnormal righting response IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:10444330 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:17019651 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20150827 MGI PMID:25915474 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20150827 MGI PMID:25915474 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0003938 abnormal ear development IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0004289 abnormal bony labyrinth IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0004315 absent vestibular saccule IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0004369 absent utricle IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0004426 abnormal cochlear labyrinth morphology IEA N RGD:5509061 20111215 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0004427 abnormal vestibular labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0004750 syndromic hearing loss IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20150827 MGI PMID:25915474 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20150827 MGI PMID:25915474 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0005226 abnormal vertebral arch development IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:14914015 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8242357 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20150827 MGI PMID:25915474 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20211125 MGI PMID:1638738 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0006014 dilated endolymphatic sac IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0006281 abnormal tail development IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0006286 inner ear hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20150827 MGI PMID:25915474 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:1638738 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:1638738 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0008307 short scala media IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20150827 MGI PMID:25915474 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20150827 MGI PMID:25915474 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:21752929 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0008854 bleb IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0009393 abnormal resting posture IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20150827 MGI PMID:25915474 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0009719 reduced cerebellar foliation IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21752929 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:21752929 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23226461 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0012792 abnormal rhombomere 3 morphology IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0012796 abnormal rhombomere 4 morphology IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0012800 abnormal rhombomere 5 morphology IAGP N RGD:5509061 20141003 MGI PMID:10842066 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:25915474 1312427 Lmx1a LIM homeobox transcription factor 1 alpha gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:25915474 1312430 Rbpjl recombination signal binding protein for immunoglobulin kappa J region-like gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1312430 Rbpjl recombination signal binding protein for immunoglobulin kappa J region-like gene MP:0001410 head bobbing IEA N RGD:5509061 20200402 MGI 1312430 Rbpjl recombination signal binding protein for immunoglobulin kappa J region-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10502683 1312430 Rbpjl recombination signal binding protein for immunoglobulin kappa J region-like gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20181227 MGI 1312434 Lactb lactamase, beta gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1312434 Lactb lactamase, beta gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1312434 Lactb lactamase, beta gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20181227 MGI 1312434 Lactb lactamase, beta gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1312434 Lactb lactamase, beta gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20181227 MGI 1312434 Lactb lactamase, beta gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20190502 MGI 1312434 Lactb lactamase, beta gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1312434 Lactb lactamase, beta gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20181227 MGI 1312434 Lactb lactamase, beta gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1312437 Fam43a family with sequence similarity 43, member A gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1312437 Fam43a family with sequence similarity 43, member A gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1312442 Tmem222 transmembrane protein 222 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20181227 MGI 1312442 Tmem222 transmembrane protein 222 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1312442 Tmem222 transmembrane protein 222 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1312444 Cenpb centromere protein B gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10645947 1312444 Cenpb centromere protein B gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:10645947 1312444 Cenpb centromere protein B gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:15016956 1312444 Cenpb centromere protein B gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10645947 1312444 Cenpb centromere protein B gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:10645947 1312444 Cenpb centromere protein B gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9548711 1312444 Cenpb centromere protein B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10645947 1312444 Cenpb centromere protein B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9548711 1312444 Cenpb centromere protein B gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10645947 1312444 Cenpb centromere protein B gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:10645947 1312444 Cenpb centromere protein B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9740654 1312444 Cenpb centromere protein B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9933410 1312444 Cenpb centromere protein B gene MP:0002292 abnormal gestational length IAGP N RGD:5509061 20141003 MGI PMID:10645947 1312444 Cenpb centromere protein B gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:9548711 1312444 Cenpb centromere protein B gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:10645947 1312444 Cenpb centromere protein B gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:10645947 1312444 Cenpb centromere protein B gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:15016956 1312444 Cenpb centromere protein B gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:10645947 1312444 Cenpb centromere protein B gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:10645947 1312444 Cenpb centromere protein B gene MP:0009096 decreased endometrial gland number IAGP N RGD:5509061 20141003 MGI PMID:10645947 1312444 Cenpb centromere protein B gene MP:0012008 delayed parturition IAGP N RGD:5509061 20141003 MGI PMID:10645947 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0001148 enlarged testis IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25336629 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0003917 increased kidney weight IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20210826 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0010935 increased airway resistance IEA N RGD:5509061 20211021 MGI 1312446 Apbb1ip amyloid beta precursor protein binding family B member 1 interacting protein gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20210826 MGI 1312450 B3galnt1 UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 1 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:11463849 1312450 B3galnt1 UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1312450 B3galnt1 UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 1 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11463849 1312454 Dguok deoxyguanosine kinase gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220811 MGI 1312454 Dguok deoxyguanosine kinase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0001263 weight loss IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20190502 MGI 1312454 Dguok deoxyguanosine kinase gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20190502 MGI 1312454 Dguok deoxyguanosine kinase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1312454 Dguok deoxyguanosine kinase gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1312454 Dguok deoxyguanosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0002833 increased heart weight IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220811 MGI 1312454 Dguok deoxyguanosine kinase gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0005516 enhanced liver regeneration IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1312454 Dguok deoxyguanosine kinase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 1312454 Dguok deoxyguanosine kinase gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1312454 Dguok deoxyguanosine kinase gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0012017 grizzled coat color IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0014388 decreased hepatocyte mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0014389 decreased skeletal muscle fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0014390 decreased myocardial fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:31127938 1312454 Dguok deoxyguanosine kinase gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20201022 MGI PMID:31127938 1312456 Gga2 golgi associated, gamma adaptin ear containing, ARF binding protein 2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:22291915 1312456 Gga2 golgi associated, gamma adaptin ear containing, ARF binding protein 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:22291915 1312456 Gga2 golgi associated, gamma adaptin ear containing, ARF binding protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22291915 1312456 Gga2 golgi associated, gamma adaptin ear containing, ARF binding protein 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22291915 1312456 Gga2 golgi associated, gamma adaptin ear containing, ARF binding protein 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22291915 1312458 S1pr4 sphingosine-1-phosphate receptor 4 gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20686109 1312458 S1pr4 sphingosine-1-phosphate receptor 4 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20686109 1312458 S1pr4 sphingosine-1-phosphate receptor 4 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20111116 MGI 1312458 S1pr4 sphingosine-1-phosphate receptor 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IEA N RGD:5509061 20111116 MGI 1312460 Frmd3 FERM domain containing 3 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1312460 Frmd3 FERM domain containing 3 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20220811 MGI 1312460 Frmd3 FERM domain containing 3 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210520 MGI 1312460 Frmd3 FERM domain containing 3 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230601 MGI 1312463 Tll2 tolloid-like 2 gene MP:0003397 increased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:18286185 1312466 Tcaf2 TRPM8 channel-associated factor 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1312466 Tcaf2 TRPM8 channel-associated factor 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1312466 Tcaf2 TRPM8 channel-associated factor 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1312466 Tcaf2 TRPM8 channel-associated factor 2 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1312466 Tcaf2 TRPM8 channel-associated factor 2 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1312466 Tcaf2 TRPM8 channel-associated factor 2 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230601 MGI 1312466 Tcaf2 TRPM8 channel-associated factor 2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1312466 Tcaf2 TRPM8 channel-associated factor 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1312466 Tcaf2 TRPM8 channel-associated factor 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1312466 Tcaf2 TRPM8 channel-associated factor 2 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20230601 MGI 1312466 Tcaf2 TRPM8 channel-associated factor 2 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20230601 MGI 1312466 Tcaf2 TRPM8 channel-associated factor 2 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20230601 MGI 1312472 Trmt9b tRNA methyltransferase 9B gene MP:0001304 cataract IEA N RGD:5509061 20200514 MGI 1312474 Tmc4 transmembrane channel-like gene family 4 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1312474 Tmc4 transmembrane channel-like gene family 4 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1312474 Tmc4 transmembrane channel-like gene family 4 gene MP:0001985 abnormal gustatory system physiology IAGP N RGD:5509061 20220421 MGI PMID:34429071 1312474 Tmc4 transmembrane channel-like gene family 4 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1312474 Tmc4 transmembrane channel-like gene family 4 gene MP:0004212 abnormal salty taste sensitivity IAGP N RGD:5509061 20220421 MGI PMID:34429071 1312474 Tmc4 transmembrane channel-like gene family 4 gene MP:0005655 increased aggression IEA N RGD:5509061 20240523 MGI 1312485 Cdc23 CDC23 cell division cycle 23 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1312485 Cdc23 CDC23 cell division cycle 23 gene MP:0001926 female infertility IAGP N RGD:5509061 20240314 MGI PMID:37768355 1312485 Cdc23 CDC23 cell division cycle 23 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1312485 Cdc23 CDC23 cell division cycle 23 gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20240314 MGI PMID:37768355 1312485 Cdc23 CDC23 cell division cycle 23 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312485 Cdc23 CDC23 cell division cycle 23 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1312486 Palld palladin, cytoskeletal associated protein gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15950489 1312486 Palld palladin, cytoskeletal associated protein gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:15950489 1312486 Palld palladin, cytoskeletal associated protein gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:15950489 1312486 Palld palladin, cytoskeletal associated protein gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15950489 1312486 Palld palladin, cytoskeletal associated protein gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:15950489 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22241836 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:22402282 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22241836 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22402282 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:22402282 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:22241836 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:22241836 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:22241836 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0002078 abnormal glucose homeostasis IEA N RGD:5509061 20141003 MGI 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22241836 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22241836 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22241836 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22402282 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201231 MGI 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0005014 increased B cell number IEA N RGD:5509061 20160804 MGI 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0005102 abnormal iris pigmentation IEA N RGD:5509061 20141003 MGI 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0005316 abnormal response to tactile stimuli IEA N RGD:5509061 20141003 MGI 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22241836 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22241836 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22402282 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22241836 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22241836 1312489 Kdm8 lysine (K)-specific demethylase 8 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1312491 Fam136a family with sequence similarity 136, member A gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20240215 MGI PMID:37461313 1312496 Med13 mediator complex subunit 13 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22541436 1312496 Med13 mediator complex subunit 13 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22541436 1312496 Med13 mediator complex subunit 13 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22541436 1312496 Med13 mediator complex subunit 13 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22541436 1312496 Med13 mediator complex subunit 13 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22541436 1312496 Med13 mediator complex subunit 13 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:22541436 1312496 Med13 mediator complex subunit 13 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22541436 1312496 Med13 mediator complex subunit 13 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22541436 1312496 Med13 mediator complex subunit 13 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22541436 1312496 Med13 mediator complex subunit 13 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22541436 1312496 Med13 mediator complex subunit 13 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22541436 1312496 Med13 mediator complex subunit 13 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22541436 1312496 Med13 mediator complex subunit 13 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22541436 1312496 Med13 mediator complex subunit 13 gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20170202 MGI PMID:22541436 1312499 Il4i1 interleukin 4 induced 1 gene MP:0001454 abnormal cued conditioning behavior IEA N RGD:5509061 20111116 MGI 1312499 Il4i1 interleukin 4 induced 1 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20210128 MGI 1312499 Il4i1 interleukin 4 induced 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1312499 Il4i1 interleukin 4 induced 1 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20150219 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20150219 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:16906134 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16906134 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16906134 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20150219 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20180927 MGI PMID:29769718 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150219 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150219 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16906134 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20180927 MGI PMID:29769718 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:16906134 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16906134 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20150219 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0002188 small heart IAGP N RGD:5509061 20150219 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20150219 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20180927 MGI PMID:29769718 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20150219 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:16906134 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:16906134 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20150219 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20150219 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20150219 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20150219 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0010688 hair follicle outer root sheath hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16906134 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180927 MGI PMID:29769718 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:25422440 1312501 Aars1 alanyl-tRNA synthetase 1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:25422440 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23583642 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:23583642 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23583642 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23583642 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:23583642 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23583642 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:23583642 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0010995 abnormal lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0011078 increased macrophage cytokine production IAGP N RGD:5509061 20141003 MGI PMID:23583642 1312503 Rc3h2 ring finger and CCCH-type zinc finger domains 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23583643 1312506 Calhm6 calcium homeostasis modulator family member 6 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20211021 MGI 1312510 Hdac2 histone deacetylase 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20150205 MGI PMID:23696608 1312510 Hdac2 histone deacetylase 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:17322895 1312510 Hdac2 histone deacetylase 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20240118 MGI PMID:17322895 1312510 Hdac2 histone deacetylase 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20194438 1312510 Hdac2 histone deacetylase 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20571512 1312510 Hdac2 histone deacetylase 2 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:17909008 1312510 Hdac2 histone deacetylase 2 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20141218 MGI PMID:23792463 1312510 Hdac2 histone deacetylase 2 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141218 MGI PMID:23792463 1312510 Hdac2 histone deacetylase 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:20194438 1312510 Hdac2 histone deacetylase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:19424149 1312510 Hdac2 histone deacetylase 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17909008 1312510 Hdac2 histone deacetylase 2 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141218 MGI PMID:23792463 1312510 Hdac2 histone deacetylase 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141218 MGI PMID:23792463 1312510 Hdac2 histone deacetylase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17909008 1312510 Hdac2 histone deacetylase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17322895 1312510 Hdac2 histone deacetylase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19424149 1312510 Hdac2 histone deacetylase 2 gene MP:0001267 enlarged chest IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141218 MGI PMID:23792463 1312510 Hdac2 histone deacetylase 2 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20240523 MGI 1312510 Hdac2 histone deacetylase 2 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20240523 MGI 1312510 Hdac2 histone deacetylase 2 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141218 MGI PMID:23792463 1312510 Hdac2 histone deacetylase 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17322895 1312510 Hdac2 histone deacetylase 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17639084 1312510 Hdac2 histone deacetylase 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20571512 1312510 Hdac2 histone deacetylase 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17322895 1312510 Hdac2 histone deacetylase 2 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20571512 1312510 Hdac2 histone deacetylase 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:17639084 1312510 Hdac2 histone deacetylase 2 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20194438 1312510 Hdac2 histone deacetylase 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:19424149 1312510 Hdac2 histone deacetylase 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17909008 1312510 Hdac2 histone deacetylase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20571512 1312510 Hdac2 histone deacetylase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141218 MGI PMID:23792463 1312510 Hdac2 histone deacetylase 2 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:17322895 1312510 Hdac2 histone deacetylase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17639084 1312510 Hdac2 histone deacetylase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19605684 1312510 Hdac2 histone deacetylase 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:17909008 1312510 Hdac2 histone deacetylase 2 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:17322895 1312510 Hdac2 histone deacetylase 2 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20571512 1312510 Hdac2 histone deacetylase 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20571512 1312510 Hdac2 histone deacetylase 2 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:17322895 1312510 Hdac2 histone deacetylase 2 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19424149 1312510 Hdac2 histone deacetylase 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:20194438 1312510 Hdac2 histone deacetylase 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20571512 1312510 Hdac2 histone deacetylase 2 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17639084 1312510 Hdac2 histone deacetylase 2 gene MP:0003429 insensitivity to growth hormone IAGP N RGD:5509061 20141003 MGI PMID:17909008 1312510 Hdac2 histone deacetylase 2 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17639084 1312510 Hdac2 histone deacetylase 2 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17639084 1312510 Hdac2 histone deacetylase 2 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0004027 trisomy IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20571512 1312510 Hdac2 histone deacetylase 2 gene MP:0004093 diffuse Z line IAGP N RGD:5509061 20180531 MGI PMID:17322895 1312510 Hdac2 histone deacetylase 2 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17909008 1312510 Hdac2 histone deacetylase 2 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:17909008 1312510 Hdac2 histone deacetylase 2 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17909008 1312510 Hdac2 histone deacetylase 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20194438 1312510 Hdac2 histone deacetylase 2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20194438 1312510 Hdac2 histone deacetylase 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:17322895 1312510 Hdac2 histone deacetylase 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:20571512 1312510 Hdac2 histone deacetylase 2 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141218 MGI PMID:23792463 1312510 Hdac2 histone deacetylase 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17322895 1312510 Hdac2 histone deacetylase 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17639084 1312510 Hdac2 histone deacetylase 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20150205 MGI PMID:23696608 1312510 Hdac2 histone deacetylase 2 gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21474102 1312510 Hdac2 histone deacetylase 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20571512 1312510 Hdac2 histone deacetylase 2 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20571512 1312510 Hdac2 histone deacetylase 2 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:17639084 1312510 Hdac2 histone deacetylase 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20194438 1312510 Hdac2 histone deacetylase 2 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20194438 1312510 Hdac2 histone deacetylase 2 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20571512 1312510 Hdac2 histone deacetylase 2 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:19424149 1312510 Hdac2 histone deacetylase 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17909008 1312510 Hdac2 histone deacetylase 2 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20194438 1312510 Hdac2 histone deacetylase 2 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17909008 1312510 Hdac2 histone deacetylase 2 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19424149 1312510 Hdac2 histone deacetylase 2 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:23287868 1312510 Hdac2 histone deacetylase 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:20194438 1312510 Hdac2 histone deacetylase 2 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19424149 1312510 Hdac2 histone deacetylase 2 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:17639084 1312510 Hdac2 histone deacetylase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17322895 1312510 Hdac2 histone deacetylase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17639084 1312510 Hdac2 histone deacetylase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17639084 1312510 Hdac2 histone deacetylase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20150205 MGI PMID:23696608 1312510 Hdac2 histone deacetylase 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20194438 1312510 Hdac2 histone deacetylase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1312510 Hdac2 histone deacetylase 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17322895 1312510 Hdac2 histone deacetylase 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19424149 1312510 Hdac2 histone deacetylase 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17909008 1312510 Hdac2 histone deacetylase 2 gene MP:0011394 increased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20240118 MGI PMID:17322895 1312510 Hdac2 histone deacetylase 2 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20571512 1312510 Hdac2 histone deacetylase 2 gene MP:0011963 abnormal total retina thickness IAGP N RGD:5509061 20150205 MGI PMID:23696608 1312510 Hdac2 histone deacetylase 2 gene MP:0012050 decreased susceptilbility to retina ischemic injury IAGP N RGD:5509061 20150205 MGI PMID:23696608 1312510 Hdac2 histone deacetylase 2 gene MP:0012404 abnormal nail color IAGP N RGD:5509061 20141218 MGI PMID:23792463 1312510 Hdac2 histone deacetylase 2 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:20194438 1312510 Hdac2 histone deacetylase 2 gene MP:0013916 decreased intestine length IAGP N RGD:5509061 20180719 MGI PMID:17909008 1312510 Hdac2 histone deacetylase 2 gene MP:0030564 thick myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:17322895 1312513 Ctdspl CTD small phosphatase like gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20160421 MGI 1312513 Ctdspl CTD small phosphatase like gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1312513 Ctdspl CTD small phosphatase like gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1312513 Ctdspl CTD small phosphatase like gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 1312516 Uck2 uridine-cytidine kinase 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 1312516 Uck2 uridine-cytidine kinase 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1312516 Uck2 uridine-cytidine kinase 2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1312518 Ercc4 excision repair cross-complementing rodent repair deficiency, complementation group 4 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:14729965 1312518 Ercc4 excision repair cross-complementing rodent repair deficiency, complementation group 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14729965 1312518 Ercc4 excision repair cross-complementing rodent repair deficiency, complementation group 4 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1312518 Ercc4 excision repair cross-complementing rodent repair deficiency, complementation group 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14729965 1312518 Ercc4 excision repair cross-complementing rodent repair deficiency, complementation group 4 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20181220 MGI PMID:14729965 1312518 Ercc4 excision repair cross-complementing rodent repair deficiency, complementation group 4 gene MP:0008402 increased cellular sensitivity to alkylating agents IAGP N RGD:5509061 20181220 MGI PMID:14729965 1312518 Ercc4 excision repair cross-complementing rodent repair deficiency, complementation group 4 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20181220 MGI PMID:14729965 1312518 Ercc4 excision repair cross-complementing rodent repair deficiency, complementation group 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1312518 Ercc4 excision repair cross-complementing rodent repair deficiency, complementation group 4 gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20181220 MGI PMID:16142233 1312518 Ercc4 excision repair cross-complementing rodent repair deficiency, complementation group 4 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14729965 1312518 Ercc4 excision repair cross-complementing rodent repair deficiency, complementation group 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1312518 Ercc4 excision repair cross-complementing rodent repair deficiency, complementation group 4 gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20181220 MGI PMID:14729965 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11604513 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:11604513 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:11604513 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11604513 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11604513 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:11604513 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11604513 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20150611 MGI PMID:18773073 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20141003 MGI PMID:11604513 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22427636 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11604513 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22427636 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0002403 abnormal pre-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22427636 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:11604513 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0004838 abnormal neural fold elevation formation IAGP N RGD:5509061 20141003 MGI PMID:11604513 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22427636 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0005022 abnormal immature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22427636 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22427636 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20150611 MGI PMID:18773073 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0005432 abnormal pro-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22427636 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:22427636 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22427636 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22427636 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:22427636 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22427636 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11604513 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20150611 MGI PMID:18773073 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0013207 absent endoderm IAGP N RGD:5509061 20141003 MGI PMID:11604513 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0014403 decreased early pro-B cell number IAGP N RGD:5509061 20240405 MGI PMID:22427636 1312525 Smarcc1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 gene MP:0014404 decreased late pro-B cell number IAGP N RGD:5509061 20240405 MGI PMID:22427636 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0003109 short femur IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0010702 split cervical atlas IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0010703 split cervical axis IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0010730 absent odontoid process IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312527 Cdk10 cyclin dependent kinase 10 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20181025 MGI PMID:28886341 1312530 Dlx2 distal-less homeobox 2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:12902388 1312530 Dlx2 distal-less homeobox 2 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1312530 Dlx2 distal-less homeobox 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20171026 MGI PMID:18697905 1312530 Dlx2 distal-less homeobox 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0001068 abnormal mandibular nerve branching IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:12902388 1312530 Dlx2 distal-less homeobox 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:12902388 1312530 Dlx2 distal-less homeobox 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12902388 1312530 Dlx2 distal-less homeobox 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12902388 1312530 Dlx2 distal-less homeobox 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1312530 Dlx2 distal-less homeobox 2 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20171005 MGI PMID:18697905 1312530 Dlx2 distal-less homeobox 2 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:12902388 1312530 Dlx2 distal-less homeobox 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1312530 Dlx2 distal-less homeobox 2 gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0004456 small pterygoid bone IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0004666 absent stapedial artery IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1312530 Dlx2 distal-less homeobox 2 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:18697905 1312530 Dlx2 distal-less homeobox 2 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0009882 absent palatal shelf IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1312530 Dlx2 distal-less homeobox 2 gene MP:0009917 abnormal hyoid bone body morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1312530 Dlx2 distal-less homeobox 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20151224 MGI PMID:24507192 1312530 Dlx2 distal-less homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12902388 1312530 Dlx2 distal-less homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20151224 MGI PMID:24507192 1312530 Dlx2 distal-less homeobox 2 gene MP:0030108 abnormal incudostapedial joint morphology IAGP N RGD:5509061 20171005 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0030108 abnormal incudostapedial joint morphology IAGP N RGD:5509061 20171005 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0030127 small stapes IAGP N RGD:5509061 20170928 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0030395 absent incus short process IAGP N RGD:5509061 20171207 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0030395 absent incus short process IAGP N RGD:5509061 20171207 MGI PMID:9187081 1312530 Dlx2 distal-less homeobox 2 gene MP:0030406 absent stapes obturator foramen IAGP N RGD:5509061 20171207 MGI PMID:7590232 1312530 Dlx2 distal-less homeobox 2 gene MP:0030406 absent stapes obturator foramen IAGP N RGD:5509061 20171207 MGI PMID:9187081 1312533 Capn7 calpain 7 gene MP:0001262 decreased body weight IEA N RGD:5509061 20111116 MGI 1312533 Capn7 calpain 7 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 1312533 Capn7 calpain 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1312536 Slf1 SMC5-SMC6 complex localization factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15632077 1312538 Vps39 VPS39 HOPS complex subunit gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20211104 MGI PMID:20961651 1312538 Vps39 VPS39 HOPS complex subunit gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20211104 MGI PMID:20961651 1312540 Sh3glb1 SH3-domain GRB2-like B1 (endophilin) gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16227588 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:17608689 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17608689 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17608689 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:17608689 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0001346 abnormal lacrimal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17898284 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12752681 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23974926 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17608689 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17898284 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:17608689 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23974926 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17608689 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12023342 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12752681 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:23974926 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:17608689 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:17608689 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:12752681 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:17608689 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0005014 increased B cell number IEA N RGD:5509061 20181011 MGI 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12023342 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12752681 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17608689 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17898284 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12023342 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:12752681 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12023342 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17244673 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17608689 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17898284 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008083 decreased single-positive T cell number IEA N RGD:5509061 20181011 MGI 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008206 increased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:17608689 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:17608689 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12752681 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12023342 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12752681 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:12023342 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12752681 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:12752681 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12023342 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:12752681 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:12023342 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:17898284 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:12023342 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:17898284 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12752681 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12752681 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0013452 increased lacrimal gland apoptosis IAGP N RGD:5509061 20150205 MGI PMID:17898284 1312547 Tnfrsf9 tumor necrosis factor receptor superfamily, member 9 gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:17608689 1312549 Tfap2d transcription factor AP-2, delta gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21858141 1312549 Tfap2d transcription factor AP-2, delta gene MP:0009039 absent inferior colliculus IAGP N RGD:5509061 20141003 MGI PMID:21858141 1312553 Lrrtm3 leucine rich repeat transmembrane neuronal 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180920 MGI PMID:22710909 1312553 Lrrtm3 leucine rich repeat transmembrane neuronal 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20180920 MGI PMID:26776509 1312553 Lrrtm3 leucine rich repeat transmembrane neuronal 3 gene MP:0002915 abnormal synaptic depression IAGP N RGD:5509061 20180920 MGI PMID:26776509 1312553 Lrrtm3 leucine rich repeat transmembrane neuronal 3 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20180920 MGI PMID:26776509 1312553 Lrrtm3 leucine rich repeat transmembrane neuronal 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20180920 MGI PMID:26776509 1312553 Lrrtm3 leucine rich repeat transmembrane neuronal 3 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20180920 MGI PMID:26776509 1312553 Lrrtm3 leucine rich repeat transmembrane neuronal 3 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20180920 MGI PMID:26776509 1312553 Lrrtm3 leucine rich repeat transmembrane neuronal 3 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20180920 MGI PMID:26776509 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20160804 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190704 MGI PMID:26854227 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20190704 MGI PMID:26854227 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0002747 abnormal aortic valve morphology IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20160804 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20190704 MGI PMID:26854227 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0004160 retroesophageal right subclavian artery IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20190704 MGI PMID:26854227 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0005244 hemopericardium IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20190704 MGI PMID:26854227 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0008922 abnormal cervical rib IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0008923 thoracoschisis IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20190704 MGI PMID:26854227 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20190704 MGI PMID:26854227 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0009820 abnormal liver vasculature morphology IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20190704 MGI PMID:26854227 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0010490 abnormal inferior vena cava valve morphology IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0011513 abnormal vertebral artery morphology IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20190704 MGI PMID:26854227 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20190704 MGI PMID:26854227 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0013875 increased trigeminal neuroma incidence IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0013878 abnormal ductus venosus valve topology IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0013936 abnormal thymus topology IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0013975 abnormal coronary sinus connection IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0014018 embryo tumor IEA N RGD:5509061 20171228 MGI 1312558 Prmt7 protein arginine N-methyltransferase 7 gene MP:0014021 heterochrony IEA N RGD:5509061 20171228 MGI 1312563 Ifit1bl2 interferon induced protein with tetratricopeptide repeats 1B like 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1312563 Ifit1bl2 interferon induced protein with tetratricopeptide repeats 1B like 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20200514 MGI 1312565 Mrtfa myocardin related transcription factor A gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22279050 1312565 Mrtfa myocardin related transcription factor A gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0001881 abnormal mammary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:16847332 1312565 Mrtfa myocardin related transcription factor A gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:22279050 1312565 Mrtfa myocardin related transcription factor A gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:22279050 1312565 Mrtfa myocardin related transcription factor A gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:22279050 1312565 Mrtfa myocardin related transcription factor A gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:16847332 1312565 Mrtfa myocardin related transcription factor A gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:16847332 1312565 Mrtfa myocardin related transcription factor A gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0009410 abnormal skeletal muscle satellite cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22279050 1312565 Mrtfa myocardin related transcription factor A gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20150402 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20150402 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:22279050 1312565 Mrtfa myocardin related transcription factor A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22279050 1312565 Mrtfa myocardin related transcription factor A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0011707 impaired fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:20534669 1312565 Mrtfa myocardin related transcription factor A gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:22279050 1312565 Mrtfa myocardin related transcription factor A gene MP:0013718 galactostasis IAGP N RGD:5509061 20150402 MGI PMID:16847332 1312565 Mrtfa myocardin related transcription factor A gene MP:0013718 galactostasis IAGP N RGD:5509061 20150402 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0013719 pale mammary gland IAGP N RGD:5509061 20150402 MGI PMID:16847332 1312565 Mrtfa myocardin related transcription factor A gene MP:0013719 pale mammary gland IAGP N RGD:5509061 20150402 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0013778 abnormal mammary gland myoepithelium morphology IAGP N RGD:5509061 20150611 MGI PMID:16847332 1312565 Mrtfa myocardin related transcription factor A gene MP:0013779 abnormal mammary gland myoepithelium physiology IAGP N RGD:5509061 20150611 MGI PMID:16847332 1312565 Mrtfa myocardin related transcription factor A gene MP:0013779 abnormal mammary gland myoepithelium physiology IAGP N RGD:5509061 20150611 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0014126 increased mammary gland apoptosis IAGP N RGD:5509061 20160317 MGI PMID:16847332 1312565 Mrtfa myocardin related transcription factor A gene MP:0014126 increased mammary gland apoptosis IAGP N RGD:5509061 20160317 MGI PMID:16847333 1312565 Mrtfa myocardin related transcription factor A gene MP:0014342 abnormal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:16847333 1312568 Dlx3 distal-less homeobox 3 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20231207 MGI 1312568 Dlx3 distal-less homeobox 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1312568 Dlx3 distal-less homeobox 3 gene MP:0000288 abnormal pericardium morphology IAGP N RGD:5509061 20141003 MGI PMID:9874789 1312568 Dlx3 distal-less homeobox 3 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18684741 1312568 Dlx3 distal-less homeobox 3 gene MP:0000392 accelerated hair follicle regression IAGP N RGD:5509061 20141003 MGI PMID:18684741 1312568 Dlx3 distal-less homeobox 3 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:18684741 1312568 Dlx3 distal-less homeobox 3 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:18684741 1312568 Dlx3 distal-less homeobox 3 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18684741 1312568 Dlx3 distal-less homeobox 3 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:18684741 1312568 Dlx3 distal-less homeobox 3 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18684741 1312568 Dlx3 distal-less homeobox 3 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:18684741 1312568 Dlx3 distal-less homeobox 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18684741 1312568 Dlx3 distal-less homeobox 3 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:9874789 1312568 Dlx3 distal-less homeobox 3 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:9874789 1312568 Dlx3 distal-less homeobox 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9874789 1312568 Dlx3 distal-less homeobox 3 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:18684741 1312568 Dlx3 distal-less homeobox 3 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1312568 Dlx3 distal-less homeobox 3 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1312568 Dlx3 distal-less homeobox 3 gene MP:0002188 small heart IEA N RGD:5509061 20210128 MGI 1312568 Dlx3 distal-less homeobox 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1312568 Dlx3 distal-less homeobox 3 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:9874789 1312568 Dlx3 distal-less homeobox 3 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:18684741 1312568 Dlx3 distal-less homeobox 3 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:18684741 1312568 Dlx3 distal-less homeobox 3 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1312568 Dlx3 distal-less homeobox 3 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9874789 1312568 Dlx3 distal-less homeobox 3 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9874789 1312568 Dlx3 distal-less homeobox 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18684741 1312568 Dlx3 distal-less homeobox 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9874789 1312568 Dlx3 distal-less homeobox 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312568 Dlx3 distal-less homeobox 3 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1312568 Dlx3 distal-less homeobox 3 gene MP:0030574 increased hair follicle cell proliferation IAGP N RGD:5509061 20181129 MGI PMID:18684741 1312573 Atg2b autophagy related 2B gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210128 MGI 1312573 Atg2b autophagy related 2B gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 1312573 Atg2b autophagy related 2B gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1312573 Atg2b autophagy related 2B gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20220811 MGI 1312573 Atg2b autophagy related 2B gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 1312573 Atg2b autophagy related 2B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1312573 Atg2b autophagy related 2B gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1312576 Dcaf15 DDB1 and CUL4 associated factor 15 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20231207 MGI 1312576 Dcaf15 DDB1 and CUL4 associated factor 15 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20231207 MGI 1312576 Dcaf15 DDB1 and CUL4 associated factor 15 gene MP:0000154 rib fusion IEA N RGD:5509061 20231207 MGI 1312576 Dcaf15 DDB1 and CUL4 associated factor 15 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20231207 MGI 1312576 Dcaf15 DDB1 and CUL4 associated factor 15 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20231207 MGI 1312576 Dcaf15 DDB1 and CUL4 associated factor 15 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20231207 MGI 1312577 Cts6 cathepsin 6 gene MP:0000745 tremors IEA N RGD:5509061 20190502 MGI 1312579 Clpx caseinolytic mitochondrial matrix peptidase chaperone subunit gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191128 MGI 1312579 Clpx caseinolytic mitochondrial matrix peptidase chaperone subunit gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1312579 Clpx caseinolytic mitochondrial matrix peptidase chaperone subunit gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191128 MGI 1312579 Clpx caseinolytic mitochondrial matrix peptidase chaperone subunit gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1312579 Clpx caseinolytic mitochondrial matrix peptidase chaperone subunit gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191128 MGI 1312579 Clpx caseinolytic mitochondrial matrix peptidase chaperone subunit gene MP:0009331 absent primitive node IEA N RGD:5509061 20191128 MGI 1312579 Clpx caseinolytic mitochondrial matrix peptidase chaperone subunit gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1312579 Clpx caseinolytic mitochondrial matrix peptidase chaperone subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312579 Clpx caseinolytic mitochondrial matrix peptidase chaperone subunit gene MP:0012724 absent head fold IEA N RGD:5509061 20191128 MGI 1312579 Clpx caseinolytic mitochondrial matrix peptidase chaperone subunit gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20190502 MGI 1312580 6430548M08Rik RIKEN cDNA 6430548M08 gene gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20231207 MGI 1312580 6430548M08Rik RIKEN cDNA 6430548M08 gene gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1312580 6430548M08Rik RIKEN cDNA 6430548M08 gene gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1312580 6430548M08Rik RIKEN cDNA 6430548M08 gene gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1312580 6430548M08Rik RIKEN cDNA 6430548M08 gene gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1312580 6430548M08Rik RIKEN cDNA 6430548M08 gene gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1312584 Dscaml1 DS cell adhesion molecule like 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:19945391 1312584 Dscaml1 DS cell adhesion molecule like 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19945391 1312584 Dscaml1 DS cell adhesion molecule like 1 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19945391 1312584 Dscaml1 DS cell adhesion molecule like 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19945391 1312584 Dscaml1 DS cell adhesion molecule like 1 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19945391 1312584 Dscaml1 DS cell adhesion molecule like 1 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19945391 1312584 Dscaml1 DS cell adhesion molecule like 1 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19945391 1312584 Dscaml1 DS cell adhesion molecule like 1 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19945391 1312584 Dscaml1 DS cell adhesion molecule like 1 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19945391 1312584 Dscaml1 DS cell adhesion molecule like 1 gene MP:0008105 increased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:19945391 1312584 Dscaml1 DS cell adhesion molecule like 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19945391 1312584 Dscaml1 DS cell adhesion molecule like 1 gene MP:0014265 thick retina inner plexiform layer IAGP N RGD:5509061 20230706 MGI PMID:19945391 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20210812 MGI PMID:33484482 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20210812 MGI PMID:33484482 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0001306 small lens IAGP N RGD:5509061 20210812 MGI PMID:33484482 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21555074 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:21555074 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0003236 abnormal lens capsule morphology IAGP N RGD:5509061 20210812 MGI PMID:33484482 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20210812 MGI PMID:33484482 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0003663 abnormal thermosensation IAGP N RGD:5509061 20141003 MGI PMID:21555074 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0005199 abnormal iris pigment epithelium IAGP N RGD:5509061 20210812 MGI PMID:33484482 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210812 MGI PMID:33484482 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21555074 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0010055 abnormal sensory neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21555074 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0010259 anterior polar cataract IAGP N RGD:5509061 20210812 MGI PMID:33484482 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0010768 mortality/aging IAGP N RGD:5509061 20210812 MGI PMID:33484482 1312586 Trpm3 transient receptor potential cation channel, subfamily M, member 3 gene MP:0020486 abnormal lens topology IAGP N RGD:5509061 20210812 MGI PMID:33484482 1312587 Gpr18 G protein-coupled receptor 18 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20170525 MGI PMID:26195725 1312587 Gpr18 G protein-coupled receptor 18 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20170525 MGI PMID:26195725 1312587 Gpr18 G protein-coupled receptor 18 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20160310 MGI PMID:25348153 1312587 Gpr18 G protein-coupled receptor 18 gene MP:0008363 decreased CD8-positive, gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20160310 MGI PMID:25348153 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000239 absent common myeloid progenitor cells IAGP N RGD:5509061 20141003 MGI PMID:16702405 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:16702405 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20170518 MGI PMID:24646517 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000486 abnormal pulmonary trunk morphology IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16702405 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:16702405 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19264921 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19264921 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:19922872 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16702405 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:16702405 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19264921 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16702405 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19264921 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:16702405 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19264921 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25757017 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:19922872 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19922872 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:19922872 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16702405 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20170518 MGI PMID:24646517 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:19922872 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:19922872 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0004648 decreased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19922872 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19264921 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:16702405 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19264921 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19264921 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:19264921 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16702405 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20170518 MGI PMID:24646517 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:19264921 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:19264921 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:19264921 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19264921 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19264921 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0010432 common ventricle IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16651658 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16702405 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312591 Kat6a K(lysine) acetyltransferase 6A gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20141003 MGI PMID:22921202 1312593 Ccr8 C-C motif chemokine receptor 8 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 1312593 Ccr8 C-C motif chemokine receptor 8 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1312593 Ccr8 C-C motif chemokine receptor 8 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1312593 Ccr8 C-C motif chemokine receptor 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12496446 1312593 Ccr8 C-C motif chemokine receptor 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12574386 1312593 Ccr8 C-C motif chemokine receptor 8 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12471141 1312593 Ccr8 C-C motif chemokine receptor 8 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1312593 Ccr8 C-C motif chemokine receptor 8 gene MP:0009084 blind uterus IEA N RGD:5509061 20210826 MGI 1312593 Ccr8 C-C motif chemokine receptor 8 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1312597 Ddx31 DEAD/H box helicase 31 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20220811 MGI 1312597 Ddx31 DEAD/H box helicase 31 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1312602 Prtn3 proteinase 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20160225 MGI PMID:25180606 1312602 Prtn3 proteinase 3 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20160225 MGI PMID:25180606 1312602 Prtn3 proteinase 3 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20160225 MGI PMID:25180606 1312604 Myt1 myelin transcription factor 1 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:17928203 1312604 Myt1 myelin transcription factor 1 gene MP:0002694 abnormal pancreas secretion IAGP N RGD:5509061 20141003 MGI PMID:17928203 1312604 Myt1 myelin transcription factor 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17928203 1312604 Myt1 myelin transcription factor 1 gene MP:0003563 abnormal pancreatic alpha cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17928203 1312604 Myt1 myelin transcription factor 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:17928203 1312604 Myt1 myelin transcription factor 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17928203 1312604 Myt1 myelin transcription factor 1 gene MP:0008953 abnormal pancreatic somatostatin secretion IAGP N RGD:5509061 20141003 MGI PMID:17928203 1312604 Myt1 myelin transcription factor 1 gene MP:0009195 abnormal PP cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17928203 1312604 Myt1 myelin transcription factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21267777 1312604 Myt1 myelin transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17928203 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20240425 MGI PMID:21052544 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20160421 MGI 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:19861548 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0002546 mydriasis IEA N RGD:5509061 20190502 MGI 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:22896717 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20240425 MGI PMID:21052544 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19861548 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19966281 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22896717 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19861548 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19966281 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:19861548 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19861548 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21052544 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20190502 MGI 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0008519 thin retina outer plexiform layer IEA N RGD:5509061 20240425 MGI 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0012029 abnormal electroretinogram waveform feature IEA N RGD:5509061 20240425 MGI 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0012671 retina spots IEA N RGD:5509061 20240425 MGI 1312608 Trpm1 transient receptor potential cation channel, subfamily M, member 1 gene MP:0020439 absent b-wave IEA N RGD:5509061 20240425 MGI 1312609 Nlrc3 NLR family, CARD domain containing 3 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22863753 1312609 Nlrc3 NLR family, CARD domain containing 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22863753 1312609 Nlrc3 NLR family, CARD domain containing 3 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:22863753 1312609 Nlrc3 NLR family, CARD domain containing 3 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22863753 1312609 Nlrc3 NLR family, CARD domain containing 3 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22863753 1312609 Nlrc3 NLR family, CARD domain containing 3 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:22863753 1312609 Nlrc3 NLR family, CARD domain containing 3 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:22863753 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0001914 hemorrhage IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0004158 right aortic arch IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0004846 absent skeletal muscle IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0004938 dilated vasculature IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0006093 arteriovenous malformation IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0010572 persistent right dorsal aorta IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0010602 abnormal pulmonary valve cusp morphology IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0011697 lens vacuoles IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0013826 absent hypoglossal canal IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0013847 retropleural edema IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0013917 persistent right 6th pharyngeal arch artery IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0013953 left sided brachiocephalic trunk IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20170504 MGI 1312610 Prrc2b proline-rich coiled-coil 2B gene MP:0020500 persistent trigeminal artery IEA N RGD:5509061 20180628 MGI 1312611 Gpat2 glycerol-3-phosphate acyltransferase 2, mitochondrial gene MP:0001147 small testis IAGP N RGD:5509061 20191114 MGI PMID:30951587 1312611 Gpat2 glycerol-3-phosphate acyltransferase 2, mitochondrial gene MP:0001925 male infertility IAGP N RGD:5509061 20191114 MGI PMID:30951587 1312611 Gpat2 glycerol-3-phosphate acyltransferase 2, mitochondrial gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20191114 MGI PMID:30951587 1312611 Gpat2 glycerol-3-phosphate acyltransferase 2, mitochondrial gene MP:0005159 azoospermia IAGP N RGD:5509061 20191114 MGI PMID:30951587 1312611 Gpat2 glycerol-3-phosphate acyltransferase 2, mitochondrial gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20191114 MGI PMID:30951587 1312611 Gpat2 glycerol-3-phosphate acyltransferase 2, mitochondrial gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20191114 MGI PMID:30951587 1312611 Gpat2 glycerol-3-phosphate acyltransferase 2, mitochondrial gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20191114 MGI PMID:30951587 1312611 Gpat2 glycerol-3-phosphate acyltransferase 2, mitochondrial gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20191114 MGI PMID:30951587 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0001258 decreased body length IEA N RGD:5509061 20201022 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0002833 increased heart weight IEA N RGD:5509061 20201022 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20201022 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210520 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20201022 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20190502 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1312614 Trappc2l trafficking protein particle complex 2L gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20231207 MGI 1312616 Cog2 component of oligomeric golgi complex 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1312616 Cog2 component of oligomeric golgi complex 2 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1312616 Cog2 component of oligomeric golgi complex 2 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20160804 MGI 1312616 Cog2 component of oligomeric golgi complex 2 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1312616 Cog2 component of oligomeric golgi complex 2 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20160804 MGI 1312616 Cog2 component of oligomeric golgi complex 2 gene MP:0005571 decreased lactate dehydrogenase level IEA N RGD:5509061 20160804 MGI 1312616 Cog2 component of oligomeric golgi complex 2 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 1312616 Cog2 component of oligomeric golgi complex 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312618 Cenph centromere protein H gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20221215 MGI 1312618 Cenph centromere protein H gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312620 Ddx42 DEAD box helicase 42 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1312620 Ddx42 DEAD box helicase 42 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1312620 Ddx42 DEAD box helicase 42 gene MP:0005477 increased circulating thyroxine level IEA N RGD:5509061 20211021 MGI 1312620 Ddx42 DEAD box helicase 42 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1312620 Ddx42 DEAD box helicase 42 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312632 Optc opticin gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:22159013 1312635 Asf1b anti-silencing function 1B histone chaperone gene MP:0002497 increased IgE level IEA N RGD:5509061 20190103 MGI 1312640 Cdc27 cell division cycle 27 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1312640 Cdc27 cell division cycle 27 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1312640 Cdc27 cell division cycle 27 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1312642 Irf2 interferon regulatory factor 2 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:11114377 1312642 Irf2 interferon regulatory factor 2 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:11114377 1312642 Irf2 interferon regulatory factor 2 gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:17709541 1312642 Irf2 interferon regulatory factor 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:11114377 1312642 Irf2 interferon regulatory factor 2 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:11114377 1312642 Irf2 interferon regulatory factor 2 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:8402903 1312642 Irf2 interferon regulatory factor 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:11114377 1312642 Irf2 interferon regulatory factor 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:8402903 1312642 Irf2 interferon regulatory factor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8402903 1312642 Irf2 interferon regulatory factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8402903 1312642 Irf2 interferon regulatory factor 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8402903 1312642 Irf2 interferon regulatory factor 2 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:8402903 1312642 Irf2 interferon regulatory factor 2 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8402903 1312642 Irf2 interferon regulatory factor 2 gene MP:0005114 premature hair loss IAGP N RGD:5509061 20141003 MGI PMID:11114377 1312642 Irf2 interferon regulatory factor 2 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:11114377 1312642 Irf2 interferon regulatory factor 2 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11114377 1312642 Irf2 interferon regulatory factor 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:8402903 1312642 Irf2 interferon regulatory factor 2 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:8402903 1312642 Irf2 interferon regulatory factor 2 gene MP:0009623 enlarged inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11114377 1312642 Irf2 interferon regulatory factor 2 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11114377 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20421391 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:20421391 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:20421391 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:19578362 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:20421391 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20421391 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19578362 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20421391 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0008179 absent germinal center B cells IAGP N RGD:5509061 20141003 MGI PMID:20421391 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20421391 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:19578362 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:20421391 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20421391 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20141003 MGI PMID:20421391 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0009058 decreased interleukin-21 secretion IAGP N RGD:5509061 20141003 MGI PMID:19578362 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:20421391 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0010187 decreased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:20421391 1312644 Batf basic leucine zipper transcription factor, ATF-like gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:20421391 1312651 Fam135a family with sequence similarity 135, member A gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230119 MGI 1312651 Fam135a family with sequence similarity 135, member A gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1312651 Fam135a family with sequence similarity 135, member A gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20230119 MGI 1312651 Fam135a family with sequence similarity 135, member A gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230119 MGI 1312651 Fam135a family with sequence similarity 135, member A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1312651 Fam135a family with sequence similarity 135, member A gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1312651 Fam135a family with sequence similarity 135, member A gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230119 MGI 1312651 Fam135a family with sequence similarity 135, member A gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1312651 Fam135a family with sequence similarity 135, member A gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1312651 Fam135a family with sequence similarity 135, member A gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230119 MGI 1312651 Fam135a family with sequence similarity 135, member A gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230119 MGI 1312653 Hmx1 H6 homeobox 1 gene MP:0000023 abnormal ear position IAGP N RGD:5509061 20141003 MGI PMID:16024820 1312653 Hmx1 H6 homeobox 1 gene MP:0000023 abnormal ear position IAGP N RGD:5509061 20141003 MGI PMID:19379485 1312653 Hmx1 H6 homeobox 1 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:16024820 1312653 Hmx1 H6 homeobox 1 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:19379485 1312653 Hmx1 H6 homeobox 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19379485 1312653 Hmx1 H6 homeobox 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19379485 1312653 Hmx1 H6 homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19379485 1312653 Hmx1 H6 homeobox 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19379485 1312653 Hmx1 H6 homeobox 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:23591430 1312653 Hmx1 H6 homeobox 1 gene MP:0008383 enlarged gonial bone IAGP N RGD:5509061 20141003 MGI PMID:19379485 1312653 Hmx1 H6 homeobox 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:23591430 1312653 Hmx1 H6 homeobox 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19379485 1312653 Hmx1 H6 homeobox 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19379485 1312653 Hmx1 H6 homeobox 1 gene MP:0030119 abnormal retrotympanic process morphology IAGP N RGD:5509061 20171005 MGI PMID:19379485 1312653 Hmx1 H6 homeobox 1 gene MP:0030213 gonial bone hyperplasia IAGP N RGD:5509061 20171019 MGI PMID:19379485 1312655 Rubcnl RUN and cysteine rich domain containing beclin 1 interacting protein like gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20191010 MGI PMID:30704899 1312655 Rubcnl RUN and cysteine rich domain containing beclin 1 interacting protein like gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20191010 MGI PMID:30704899 1312655 Rubcnl RUN and cysteine rich domain containing beclin 1 interacting protein like gene MP:0002981 increased liver weight IAGP N RGD:5509061 20191010 MGI PMID:30704899 1312655 Rubcnl RUN and cysteine rich domain containing beclin 1 interacting protein like gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20191010 MGI PMID:30704899 1312655 Rubcnl RUN and cysteine rich domain containing beclin 1 interacting protein like gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20191010 MGI PMID:30704899 1312655 Rubcnl RUN and cysteine rich domain containing beclin 1 interacting protein like gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20191010 MGI PMID:30704899 1312655 Rubcnl RUN and cysteine rich domain containing beclin 1 interacting protein like gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20191010 MGI PMID:30704899 1312655 Rubcnl RUN and cysteine rich domain containing beclin 1 interacting protein like gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20191010 MGI PMID:30704899 1312657 Perm1 PPARGC1 and ESRR induced regulator, muscle 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20230406 MGI PMID:36419485 1312659 Haus3 HAUS augmin-like complex, subunit 3 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:21118569 1312668 Exoc1 exocyst complex component 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 1312668 Exoc1 exocyst complex component 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20170330 MGI PMID:26346620 1312668 Exoc1 exocyst complex component 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312668 Exoc1 exocyst complex component 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1312670 Atf7 activating transcription factor 7 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20190502 MGI 1312670 Atf7 activating transcription factor 7 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17699753 1312670 Atf7 activating transcription factor 7 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17699753 1312670 Atf7 activating transcription factor 7 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17699753 1312670 Atf7 activating transcription factor 7 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201022 MGI 1312670 Atf7 activating transcription factor 7 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19893493 1312670 Atf7 activating transcription factor 7 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:19893493 1312670 Atf7 activating transcription factor 7 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17699753 1312670 Atf7 activating transcription factor 7 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17699753 1312670 Atf7 activating transcription factor 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17699753 1312670 Atf7 activating transcription factor 7 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17699753 1312670 Atf7 activating transcription factor 7 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17699753 1312670 Atf7 activating transcription factor 7 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17699753 1312670 Atf7 activating transcription factor 7 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:17699753 1312670 Atf7 activating transcription factor 7 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17699753 1312670 Atf7 activating transcription factor 7 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17699753 1312670 Atf7 activating transcription factor 7 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:19893493 1312670 Atf7 activating transcription factor 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17699753 1312672 Hipk1 homeodomain interacting protein kinase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16537918 1312672 Hipk1 homeodomain interacting protein kinase 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16537918 1312672 Hipk1 homeodomain interacting protein kinase 1 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:16537918 1312672 Hipk1 homeodomain interacting protein kinase 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16537918 1312672 Hipk1 homeodomain interacting protein kinase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16537918 1312672 Hipk1 homeodomain interacting protein kinase 1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:12702766 1312672 Hipk1 homeodomain interacting protein kinase 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16537918 1312672 Hipk1 homeodomain interacting protein kinase 1 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:16537918 1312672 Hipk1 homeodomain interacting protein kinase 1 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:16537918 1312672 Hipk1 homeodomain interacting protein kinase 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16537918 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20844119 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:11583983 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:11583983 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:11583983 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20844119 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20844119 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20141003 MGI PMID:20844119 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11583983 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:11583983 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:11583983 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:11583983 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11583983 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:11583983 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20844119 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:20844119 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0004836 abnormal synaptic acetylcholine release IAGP N RGD:5509061 20141003 MGI PMID:20844119 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:11583983 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:11583983 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0009426 decreased soleus weight IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:11583983 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0030950 abnormal synaptic vesicle exocytosis IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312682 Col13a1 collagen, type XIII, alpha 1 gene MP:0030951 abnormal endocytosis IAGP N RGD:5509061 20190725 MGI PMID:28369367 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0000111 cleft palate IAGP N RGD:5509061 20221006 MGI PMID:35212626 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0000380 small hair follicles IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20200402 MGI PMID:27135738 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22431509 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200402 MGI PMID:27135738 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22431509 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200402 MGI PMID:27135738 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22431509 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20180607 MGI PMID:28041882 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0001260 increased body weight IAGP N RGD:5509061 20190221 MGI PMID:29244146 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0001260 increased body weight IAGP N RGD:5509061 20240328 MGI PMID:38015625 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:11390661 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:18311137 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20190221 MGI PMID:29244146 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18311137 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20211209 MGI PMID:30954472 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0001935 decreased litter size IAGP N RGD:5509061 20211209 MGI PMID:30954472 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20200402 MGI PMID:27135738 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:22431509 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20200402 MGI PMID:27135738 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0002083 premature death IAGP N RGD:5509061 20200402 MGI PMID:27135738 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11390661 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11390661 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12496962 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12496962 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20200402 MGI PMID:27135738 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0002833 increased heart weight IAGP N RGD:5509061 20190221 MGI PMID:29244146 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0002865 increased growth rate IAGP N RGD:5509061 20190221 MGI PMID:29244146 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20211209 MGI PMID:30954472 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20190221 MGI PMID:29244146 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11390661 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19026780 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:22215809 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0004514 dystocia IAGP N RGD:5509061 20211209 MGI PMID:30954472 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20211209 MGI PMID:30954472 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20190221 MGI PMID:29244146 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20240328 MGI PMID:38015625 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:22431509 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22431509 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23680150 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0005432 abnormal pro-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12496962 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:23680150 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12496962 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12496962 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:23680150 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:23680150 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:23680150 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:23680150 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:23680150 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0008755 abnormal immunoglobulin V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:12496962 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0008876 decreased uterine NK cell number IAGP N RGD:5509061 20211209 MGI PMID:30954472 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20211209 MGI PMID:30954472 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0009094 abnormal endometrial gland morphology IAGP N RGD:5509061 20211209 MGI PMID:30954472 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19755104 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20160804 MGI 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20200402 MGI PMID:27135738 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0010682 abnormal hair follicle infundibulum morphology IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0010684 abnormal hair follicle outer root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20190221 MGI PMID:29244146 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22215809 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20190221 MGI PMID:29244146 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12496962 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11390661 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18311137 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19026780 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20240328 MGI PMID:38015625 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0011195 increased hair follicle apoptosis IAGP N RGD:5509061 20181129 MGI PMID:21317239 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0011873 enlarged uterine horn IAGP N RGD:5509061 20211209 MGI PMID:30954472 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:11390661 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0013401 increased endometrial gland number IAGP N RGD:5509061 20211209 MGI PMID:30954472 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0013438 dysmyelination IAGP N RGD:5509061 20180607 MGI PMID:28041882 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0013620 increased internal diameter of femur IAGP N RGD:5509061 20240328 MGI PMID:38015625 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0013623 increased femur compact bone thickness IAGP N RGD:5509061 20240328 MGI PMID:38015625 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0014519 myocardial ventricular hypertrabeculation IAGP N RGD:5509061 20240822 MGI PMID:22215809 1312684 Ezh2 enhancer of zeste 2 polycomb repressive complex 2 subunit gene MP:0031336 abnormal uterine epithelium development IAGP N RGD:5509061 20220120 MGI PMID:30954472 1312686 Card10 caspase recruitment domain family, member 10 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:17438001 1312686 Card10 caspase recruitment domain family, member 10 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17438001 1312688 Il21r interleukin 21 receptor gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:17077330 1312688 Il21r interleukin 21 receptor gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:17077330 1312688 Il21r interleukin 21 receptor gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 1312688 Il21r interleukin 21 receptor gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20111116 MGI 1312688 Il21r interleukin 21 receptor gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17077330 1312688 Il21r interleukin 21 receptor gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:16778988 1312688 Il21r interleukin 21 receptor gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12446913 1312688 Il21r interleukin 21 receptor gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12446913 1312688 Il21r interleukin 21 receptor gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:17077330 1312688 Il21r interleukin 21 receptor gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:11970879 1312688 Il21r interleukin 21 receptor gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1312688 Il21r interleukin 21 receptor gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1312688 Il21r interleukin 21 receptor gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19075398 1312688 Il21r interleukin 21 receptor gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17077330 1312688 Il21r interleukin 21 receptor gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11970879 1312688 Il21r interleukin 21 receptor gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12446913 1312688 Il21r interleukin 21 receptor gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17077330 1312688 Il21r interleukin 21 receptor gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:19075398 1312688 Il21r interleukin 21 receptor gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11970879 1312688 Il21r interleukin 21 receptor gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12446913 1312688 Il21r interleukin 21 receptor gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:17077330 1312688 Il21r interleukin 21 receptor gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:17077330 1312688 Il21r interleukin 21 receptor gene MP:0002607 decreased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17077330 1312688 Il21r interleukin 21 receptor gene MP:0003068 enlarged kidney IEA N RGD:5509061 20201022 MGI 1312688 Il21r interleukin 21 receptor gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:11970879 1312688 Il21r interleukin 21 receptor gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17077330 1312688 Il21r interleukin 21 receptor gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15630141 1312688 Il21r interleukin 21 receptor gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:18546146 1312688 Il21r interleukin 21 receptor gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20180111 MGI PMID:19164519 1312688 Il21r interleukin 21 receptor gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:18779574 1312688 Il21r interleukin 21 receptor gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17077330 1312688 Il21r interleukin 21 receptor gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11970879 1312688 Il21r interleukin 21 receptor gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:11970879 1312688 Il21r interleukin 21 receptor gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:15630141 1312688 Il21r interleukin 21 receptor gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18779574 1312688 Il21r interleukin 21 receptor gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19075398 1312688 Il21r interleukin 21 receptor gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:17077330 1312688 Il21r interleukin 21 receptor gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:16778988 1312688 Il21r interleukin 21 receptor gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:17077330 1312688 Il21r interleukin 21 receptor gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:19075398 1312688 Il21r interleukin 21 receptor gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11970879 1312688 Il21r interleukin 21 receptor gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17581588 1312688 Il21r interleukin 21 receptor gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17581588 1312688 Il21r interleukin 21 receptor gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18474630 1312688 Il21r interleukin 21 receptor gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18779574 1312688 Il21r interleukin 21 receptor gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11970879 1312688 Il21r interleukin 21 receptor gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12446913 1312688 Il21r interleukin 21 receptor gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16778988 1312688 Il21r interleukin 21 receptor gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:17077330 1312688 Il21r interleukin 21 receptor gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19075398 1312688 Il21r interleukin 21 receptor gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12446913 1312688 Il21r interleukin 21 receptor gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:19075398 1312688 Il21r interleukin 21 receptor gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:11970879 1312688 Il21r interleukin 21 receptor gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:12446913 1312688 Il21r interleukin 21 receptor gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:16778988 1312688 Il21r interleukin 21 receptor gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:12446913 1312688 Il21r interleukin 21 receptor gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:12446913 1312688 Il21r interleukin 21 receptor gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11970879 1312688 Il21r interleukin 21 receptor gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17581588 1312688 Il21r interleukin 21 receptor gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19075398 1312688 Il21r interleukin 21 receptor gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:16778988 1312688 Il21r interleukin 21 receptor gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:19075398 1312688 Il21r interleukin 21 receptor gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:17581537 1312688 Il21r interleukin 21 receptor gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:17581588 1312688 Il21r interleukin 21 receptor gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:18779574 1312688 Il21r interleukin 21 receptor gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:16778988 1312688 Il21r interleukin 21 receptor gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19075398 1312688 Il21r interleukin 21 receptor gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:17077330 1312688 Il21r interleukin 21 receptor gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19075398 1312688 Il21r interleukin 21 receptor gene MP:0009058 decreased interleukin-21 secretion IAGP N RGD:5509061 20141003 MGI PMID:16778988 1312688 Il21r interleukin 21 receptor gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11970879 1312691 Pianp PILR alpha associated neural protein gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0001361 social withdrawal IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0002918 abnormal paired-pulse facilitation IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0003063 increased coping response IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0010052 increased grip strength IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0030585 enhanced behavioral response to amphetamine IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312691 Pianp PILR alpha associated neural protein gene MP:0030735 abnormal glutamic acid level IAGP N RGD:5509061 20191031 MGI PMID:31511635 1312694 Pold2 polymerase (DNA directed), delta 2, regulatory subunit gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20241017 MGI PMID:36528861 1312694 Pold2 polymerase (DNA directed), delta 2, regulatory subunit gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20240613 MGI PMID:36528861 1312694 Pold2 polymerase (DNA directed), delta 2, regulatory subunit gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20240613 MGI PMID:36528861 1312694 Pold2 polymerase (DNA directed), delta 2, regulatory subunit gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20240801 MGI PMID:36528861 1312694 Pold2 polymerase (DNA directed), delta 2, regulatory subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312694 Pold2 polymerase (DNA directed), delta 2, regulatory subunit gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1312696 Armc3 armadillo repeat containing 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20211216 MGI PMID:34428398 1312696 Armc3 armadillo repeat containing 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20211216 MGI PMID:34428398 1312696 Armc3 armadillo repeat containing 3 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20211216 MGI PMID:34428398 1312696 Armc3 armadillo repeat containing 3 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20211216 MGI PMID:34428398 1312696 Armc3 armadillo repeat containing 3 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20211216 MGI PMID:34428398 1312697 Ebf3 early B cell factor 3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:14993187 1312697 Ebf3 early B cell factor 3 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:14993187 1312697 Ebf3 early B cell factor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14993187 1312697 Ebf3 early B cell factor 3 gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:14993187 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:23293286 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16690048 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:11493566 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:16690048 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11156601 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11493566 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:18321480 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:20969844 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:22609278 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11156601 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18787067 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:22609278 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:23293286 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:22609278 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:11493566 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:18787067 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:22609278 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:23481413 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001334 absent optic tract IAGP N RGD:5509061 20141003 MGI PMID:15980246 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11493566 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19459208 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11493566 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23481413 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18321480 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16690048 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:23481413 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:11493566 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23293286 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11493566 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11493566 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22609278 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18321480 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23481413 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15980246 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18321480 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21903076 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006070 increased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:18787067 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23481413 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15980246 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23481413 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15980246 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18321480 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006075 abnormal retina cone bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15980246 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006075 abnormal retina cone bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17092954 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18321480 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18787067 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11156601 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22609278 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:11156601 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:14623245 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:18321480 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:18787067 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:20969844 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:21903076 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:23293286 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:23481413 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11156601 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18321480 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008068 absent retina ganglion cell IAGP N RGD:5509061 20141003 MGI PMID:11493566 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008068 absent retina ganglion cell IAGP N RGD:5509061 20141003 MGI PMID:18787067 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008105 increased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:11156601 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008105 increased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:17092954 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:18321480 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008445 increased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:11493566 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008445 increased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:23481413 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20141003 MGI PMID:15980246 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20141003 MGI PMID:23481413 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:18321480 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008510 absent retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:11493566 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:11493566 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15980246 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:18321480 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:11493566 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:15980246 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15980246 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:18321480 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:15980246 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:20969844 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:23481413 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:11156601 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:11493566 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:23481413 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:15980246 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0020548 decreased optic chiasm size IAGP N RGD:5509061 20180301 MGI PMID:11156601 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:18321480 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:18787067 1312699 Atoh7 atonal bHLH transcription factor 7 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:23481413 1312702 Rdh13 retinol dehydrogenase 13 (all-trans and 9-cis) gene MP:0003312 abnormal locomotor coordination IEA N RGD:5509061 20170413 MGI 1312702 Rdh13 retinol dehydrogenase 13 (all-trans and 9-cis) gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22605914 1312702 Rdh13 retinol dehydrogenase 13 (all-trans and 9-cis) gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:22605914 1312702 Rdh13 retinol dehydrogenase 13 (all-trans and 9-cis) gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22605914 1312702 Rdh13 retinol dehydrogenase 13 (all-trans and 9-cis) gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22605914 1312702 Rdh13 retinol dehydrogenase 13 (all-trans and 9-cis) gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:22605914 1312702 Rdh13 retinol dehydrogenase 13 (all-trans and 9-cis) gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:22605914 1312708 Pcare photoreceptor cilium actin regulator gene MP:0001326 retina degeneration IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0009392 retina gliosis IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20160414 MGI PMID:25616964 1312708 Pcare photoreceptor cilium actin regulator gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:25616964 1312710 Aifm2 apoptosis-inducing factor, mitochondrion-associated 2 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16186796 1312712 Rhoc ras homolog family member C gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16107613 1312712 Rhoc ras homolog family member C gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16107613 1312712 Rhoc ras homolog family member C gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16107613 1312721 Stil Scl/Tal1 interrupting locus gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:10385121 1312721 Stil Scl/Tal1 interrupting locus gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10385121 1312721 Stil Scl/Tal1 interrupting locus gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11668681 1312721 Stil Scl/Tal1 interrupting locus gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10385121 1312721 Stil Scl/Tal1 interrupting locus gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10385121 1312721 Stil Scl/Tal1 interrupting locus gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:10385121 1312721 Stil Scl/Tal1 interrupting locus gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10385121 1312721 Stil Scl/Tal1 interrupting locus gene MP:0004712 notochord degeneration IAGP N RGD:5509061 20141003 MGI PMID:10385121 1312721 Stil Scl/Tal1 interrupting locus gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:10385121 1312721 Stil Scl/Tal1 interrupting locus gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:11668681 1312721 Stil Scl/Tal1 interrupting locus gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10385121 1312721 Stil Scl/Tal1 interrupting locus gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11668681 1312723 Mospd3 motile sperm domain containing 3 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15533722 1312723 Mospd3 motile sperm domain containing 3 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15533722 1312723 Mospd3 motile sperm domain containing 3 gene MP:0000486 abnormal pulmonary trunk morphology IAGP N RGD:5509061 20141003 MGI PMID:15533722 1312723 Mospd3 motile sperm domain containing 3 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15533722 1312723 Mospd3 motile sperm domain containing 3 gene MP:0004061 papillary muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15533722 1312723 Mospd3 motile sperm domain containing 3 gene MP:0010428 abnormal heart right ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:15533722 1312723 Mospd3 motile sperm domain containing 3 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20231221 MGI PMID:15533722 1312723 Mospd3 motile sperm domain containing 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15533722 1312723 Mospd3 motile sperm domain containing 3 gene MP:0021160 decreased heart right ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:15533722 1312726 Rad52 RAD52 homolog, DNA repair protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15122331 1312726 Rad52 RAD52 homolog, DNA repair protein gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:15122331 1312726 Rad52 RAD52 homolog, DNA repair protein gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15122331 1312726 Rad52 RAD52 homolog, DNA repair protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15122331 1312726 Rad52 RAD52 homolog, DNA repair protein gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16009599 1312726 Rad52 RAD52 homolog, DNA repair protein gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:16009599 1312726 Rad52 RAD52 homolog, DNA repair protein gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15122331 1312726 Rad52 RAD52 homolog, DNA repair protein gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15122331 1312726 Rad52 RAD52 homolog, DNA repair protein gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16009599 1312726 Rad52 RAD52 homolog, DNA repair protein gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15122331 1312731 Usp8 ubiquitin specific peptidase 8 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:17452457 1312731 Usp8 ubiquitin specific peptidase 8 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17452457 1312731 Usp8 ubiquitin specific peptidase 8 gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:17452457 1312731 Usp8 ubiquitin specific peptidase 8 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:17452457 1312731 Usp8 ubiquitin specific peptidase 8 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17452457 1312731 Usp8 ubiquitin specific peptidase 8 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:17452457 1312731 Usp8 ubiquitin specific peptidase 8 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17452457 1312731 Usp8 ubiquitin specific peptidase 8 gene MP:0003326 liver failure IAGP N RGD:5509061 20141003 MGI PMID:17452457 1312731 Usp8 ubiquitin specific peptidase 8 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17452457 1312731 Usp8 ubiquitin specific peptidase 8 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17452457 1312731 Usp8 ubiquitin specific peptidase 8 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:17452457 1312731 Usp8 ubiquitin specific peptidase 8 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17452457 1312735 Lpxn leupaxin gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20210617 MGI PMID:32269569 1312735 Lpxn leupaxin gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20210617 MGI PMID:32269569 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0001284 absent vibrissae IEA N RGD:5509061 20210128 MGI 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21685914 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20210128 MGI 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:21685914 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:21685914 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:21685914 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:21685914 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:21685914 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21685914 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0011344 abnormal loop of Henle ascending limb thick segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21685914 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20180222 MGI PMID:21685914 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20180222 MGI PMID:21685914 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1312739 Sec63 SEC63 homolog, protein translocation regulator gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1312743 Mettl9 methyltransferase like 9 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20210506 MGI PMID:33563959 1312745 Wnt10b wingless-type MMTV integration site family, member 10B gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1312745 Wnt10b wingless-type MMTV integration site family, member 10B gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210128 MGI 1312745 Wnt10b wingless-type MMTV integration site family, member 10B gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:15673614 1312745 Wnt10b wingless-type MMTV integration site family, member 10B gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:15673614 1312745 Wnt10b wingless-type MMTV integration site family, member 10B gene MP:0001891 hydrocephaly IEA N RGD:5509061 20181227 MGI 1312745 Wnt10b wingless-type MMTV integration site family, member 10B gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20181227 MGI 1312745 Wnt10b wingless-type MMTV integration site family, member 10B gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20190502 MGI 1312747 Tnfrsf25 tumor necrosis factor receptor superfamily, member 25 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:11313471 1312747 Tnfrsf25 tumor necrosis factor receptor superfamily, member 25 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:11313471 1312747 Tnfrsf25 tumor necrosis factor receptor superfamily, member 25 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11313471 1312747 Tnfrsf25 tumor necrosis factor receptor superfamily, member 25 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11313471 1312747 Tnfrsf25 tumor necrosis factor receptor superfamily, member 25 gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:11313471 1312747 Tnfrsf25 tumor necrosis factor receptor superfamily, member 25 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11313471 1312747 Tnfrsf25 tumor necrosis factor receptor superfamily, member 25 gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20150219 MGI PMID:24557836 1312749 Kctd5 potassium channel tetramerisation domain containing 5 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20230601 MGI 1312749 Kctd5 potassium channel tetramerisation domain containing 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1312749 Kctd5 potassium channel tetramerisation domain containing 5 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210520 MGI 1312750 Thoc5 THO complex 5 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20051105 1312750 Thoc5 THO complex 5 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20051105 1312750 Thoc5 THO complex 5 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20051105 1312750 Thoc5 THO complex 5 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:20051105 1312750 Thoc5 THO complex 5 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20051105 1312750 Thoc5 THO complex 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20051105 1312750 Thoc5 THO complex 5 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20051105 1312750 Thoc5 THO complex 5 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20051105 1312750 Thoc5 THO complex 5 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20051105 1312750 Thoc5 THO complex 5 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20051105 1312750 Thoc5 THO complex 5 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20051105 1312750 Thoc5 THO complex 5 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:20051105 1312750 Thoc5 THO complex 5 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20051105 1312750 Thoc5 THO complex 5 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20051105 1312750 Thoc5 THO complex 5 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20051105 1312754 Drg1 developmentally regulated GTP binding protein 1 gene MP:0000613 abnormal salivary gland morphology IEA N RGD:5509061 20230119 MGI 1312754 Drg1 developmentally regulated GTP binding protein 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1312754 Drg1 developmentally regulated GTP binding protein 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230119 MGI 1312754 Drg1 developmentally regulated GTP binding protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20240215 MGI PMID:37179472 1312756 Cebpz CCAAT/enhancer binding protein zeta gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1312760 Kif1a kinesin family member 1A gene MP:0000755 hindlimb paralysis IEA N RGD:5509061 20160407 MGI 1312760 Kif1a kinesin family member 1A gene MP:0001265 decreased body size IEA N RGD:5509061 20160407 MGI 1312760 Kif1a kinesin family member 1A gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9548721 1312760 Kif1a kinesin family member 1A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9548721 1312760 Kif1a kinesin family member 1A gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:9548721 1312760 Kif1a kinesin family member 1A gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:9548721 1312760 Kif1a kinesin family member 1A gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:9548721 1312760 Kif1a kinesin family member 1A gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:9548721 1312760 Kif1a kinesin family member 1A gene MP:0003312 abnormal locomotor coordination IEA N RGD:5509061 20160407 MGI 1312760 Kif1a kinesin family member 1A gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:9548721 1312760 Kif1a kinesin family member 1A gene MP:0004263 abnormal limb posture IEA N RGD:5509061 20160407 MGI 1312760 Kif1a kinesin family member 1A gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:9548721 1312760 Kif1a kinesin family member 1A gene MP:0004793 abnormal synaptic vesicle clustering IAGP N RGD:5509061 20141003 MGI PMID:9548721 1312760 Kif1a kinesin family member 1A gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:9548721 1312760 Kif1a kinesin family member 1A gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:9548721 1312760 Kif1a kinesin family member 1A gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:9548721 1312760 Kif1a kinesin family member 1A gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:9548721 1312760 Kif1a kinesin family member 1A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9548721 1312760 Kif1a kinesin family member 1A gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9548721 1312760 Kif1a kinesin family member 1A gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20160407 MGI 1312760 Kif1a kinesin family member 1A gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20160407 MGI 1312762 Sec61b SEC61 translocon subunit beta gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 1312762 Sec61b SEC61 translocon subunit beta gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1312762 Sec61b SEC61 translocon subunit beta gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20231207 MGI 1312764 Ddx21 DExD box helicase 21 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241010 MGI 1312764 Ddx21 DExD box helicase 21 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241010 MGI 1312764 Ddx21 DExD box helicase 21 gene MP:0008762 embryonic lethality IEA N RGD:5509061 20141003 MGI 1312764 Ddx21 DExD box helicase 21 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1312764 Ddx21 DExD box helicase 21 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241010 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20150122 MGI PMID:24833722 1312765 Fam161a family with sequence similarity 161, member A gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20160421 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0001488 increased startle reflex IEA N RGD:5509061 20190502 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0002090 abnormal vision IAGP N RGD:5509061 20150122 MGI PMID:24833722 1312765 Fam161a family with sequence similarity 161, member A gene MP:0002626 increased heart rate IEA N RGD:5509061 20160421 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0003064 decreased coping response IEA N RGD:5509061 20160421 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20150122 MGI PMID:24833722 1312765 Fam161a family with sequence similarity 161, member A gene MP:0003960 increased lean body mass IEA N RGD:5509061 20221215 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220811 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20240523 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20150122 MGI PMID:24833722 1312765 Fam161a family with sequence similarity 161, member A gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20150122 MGI PMID:24833722 1312765 Fam161a family with sequence similarity 161, member A gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20150122 MGI PMID:24833722 1312765 Fam161a family with sequence similarity 161, member A gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20150122 MGI PMID:24833722 1312765 Fam161a family with sequence similarity 161, member A gene MP:0008918 microgliosis IAGP N RGD:5509061 20150122 MGI PMID:24833722 1312765 Fam161a family with sequence similarity 161, member A gene MP:0010052 increased grip strength IEA N RGD:5509061 20160421 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0010507 shortened RR interval IEA N RGD:5509061 20160421 MGI 1312765 Fam161a family with sequence similarity 161, member A gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20150122 MGI PMID:24833722 1312765 Fam161a family with sequence similarity 161, member A gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20150122 MGI PMID:24833722 1312765 Fam161a family with sequence similarity 161, member A gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20150122 MGI PMID:24833722 1312765 Fam161a family with sequence similarity 161, member A gene MP:0012147 increased a-wave implicit time IAGP N RGD:5509061 20150122 MGI PMID:24833722 1312765 Fam161a family with sequence similarity 161, member A gene MP:0012150 increased b-wave implicit time IAGP N RGD:5509061 20150122 MGI PMID:24833722 1312765 Fam161a family with sequence similarity 161, member A gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20160304 MGI PMID:24833722 1312765 Fam161a family with sequence similarity 161, member A gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:24833722 1312765 Fam161a family with sequence similarity 161, member A gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:24833722 1312767 Cldn19 claudin 19 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15883201 1312767 Cldn19 claudin 19 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15883201 1312767 Cldn19 claudin 19 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15883201 1312767 Cldn19 claudin 19 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20240523 MGI 1312767 Cldn19 claudin 19 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1312767 Cldn19 claudin 19 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1312767 Cldn19 claudin 19 gene MP:0010511 shortened PR interval IEA N RGD:5509061 20211021 MGI 1312767 Cldn19 claudin 19 gene MP:0010571 shortened ST segment IEA N RGD:5509061 20210128 MGI 1312767 Cldn19 claudin 19 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20170105 MGI 1312767 Cldn19 claudin 19 gene MP:0011954 shortened PQ interval IEA N RGD:5509061 20210128 MGI 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0001147 small testis IAGP N RGD:5509061 20220324 MGI PMID:29293683 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220324 MGI PMID:29293683 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220324 MGI PMID:29293683 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0001262 decreased body weight IEA N RGD:5509061 20111116 MGI 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16314502 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23133585 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23133585 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22240097 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:23133585 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20220324 MGI PMID:29293683 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0004196 abnormal prenatal growth/weight/body size IAGP N RGD:5509061 20160331 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220324 MGI PMID:29293683 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220324 MGI PMID:29293683 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16314502 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23133585 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0005159 azoospermia IAGP N RGD:5509061 20220324 MGI PMID:29293683 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0005459 decreased percent body fat/body weight IEA N RGD:5509061 20111116 MGI 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20220324 MGI PMID:29293683 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16314502 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16314502 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:23133585 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:23133585 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23133585 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:16314502 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22240097 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16847320 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16314502 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0012159 absent anterior visceral endoderm IAGP N RGD:5509061 20141003 MGI PMID:20826531 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20220324 MGI PMID:29293683 1312772 Pknox1 Pbx/knotted 1 homeobox gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220324 MGI PMID:29293683 1312774 Sfswap splicing factor SWAP gene MP:0000026 abnormal inner ear morphology IEA N RGD:5509061 20111116 MGI 1312774 Sfswap splicing factor SWAP gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1312774 Sfswap splicing factor SWAP gene MP:0003491 abnormal voluntary movement IEA N RGD:5509061 20111116 MGI 1312774 Sfswap splicing factor SWAP gene MP:0005333 decreased heart rate IEA N RGD:5509061 20240523 MGI 1312774 Sfswap splicing factor SWAP gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1312774 Sfswap splicing factor SWAP gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20240523 MGI 1312774 Sfswap splicing factor SWAP gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1312774 Sfswap splicing factor SWAP gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1312776 Lamtor5 late endosomal/lysosomal adaptor, MAPK and MTOR activator 5 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20231207 MGI 1312776 Lamtor5 late endosomal/lysosomal adaptor, MAPK and MTOR activator 5 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20191114 MGI PMID:29259128 1312776 Lamtor5 late endosomal/lysosomal adaptor, MAPK and MTOR activator 5 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20191114 MGI PMID:29259128 1312776 Lamtor5 late endosomal/lysosomal adaptor, MAPK and MTOR activator 5 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20191114 MGI PMID:29259128 1312776 Lamtor5 late endosomal/lysosomal adaptor, MAPK and MTOR activator 5 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20191114 MGI PMID:29259128 1312776 Lamtor5 late endosomal/lysosomal adaptor, MAPK and MTOR activator 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312776 Lamtor5 late endosomal/lysosomal adaptor, MAPK and MTOR activator 5 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1312776 Lamtor5 late endosomal/lysosomal adaptor, MAPK and MTOR activator 5 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1312776 Lamtor5 late endosomal/lysosomal adaptor, MAPK and MTOR activator 5 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20191114 MGI PMID:29259128 1312776 Lamtor5 late endosomal/lysosomal adaptor, MAPK and MTOR activator 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1312780 Suclg2 succinate-Coenzyme A ligase, GDP-forming, beta subunit gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20180510 MGI PMID:27496549 1312780 Suclg2 succinate-Coenzyme A ligase, GDP-forming, beta subunit gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1312780 Suclg2 succinate-Coenzyme A ligase, GDP-forming, beta subunit gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20180510 MGI PMID:27496549 1312780 Suclg2 succinate-Coenzyme A ligase, GDP-forming, beta subunit gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180510 MGI PMID:27496549 1312780 Suclg2 succinate-Coenzyme A ligase, GDP-forming, beta subunit gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20180510 MGI PMID:27496549 1312780 Suclg2 succinate-Coenzyme A ligase, GDP-forming, beta subunit gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20180510 MGI PMID:27496549 1312780 Suclg2 succinate-Coenzyme A ligase, GDP-forming, beta subunit gene MP:0014388 decreased hepatocyte mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:27496549 1312782 Dnajc9 DnaJ heat shock protein family (Hsp40) member C9 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20181227 MGI 1312782 Dnajc9 DnaJ heat shock protein family (Hsp40) member C9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312782 Dnajc9 DnaJ heat shock protein family (Hsp40) member C9 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1312782 Dnajc9 DnaJ heat shock protein family (Hsp40) member C9 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1312784 C1qtnf3 C1q and tumor necrosis factor related protein 3 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:24269820 1312784 C1qtnf3 C1q and tumor necrosis factor related protein 3 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:24269820 1312784 C1qtnf3 C1q and tumor necrosis factor related protein 3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20221215 MGI 1312784 C1qtnf3 C1q and tumor necrosis factor related protein 3 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:24269820 1312784 C1qtnf3 C1q and tumor necrosis factor related protein 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20221215 MGI 1312784 C1qtnf3 C1q and tumor necrosis factor related protein 3 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20221215 MGI 1312793 Pabpc4 poly(A) binding protein, cytoplasmic 4 gene MP:0002833 increased heart weight IEA N RGD:5509061 20181227 MGI 1312793 Pabpc4 poly(A) binding protein, cytoplasmic 4 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20160114 MGI 1312793 Pabpc4 poly(A) binding protein, cytoplasmic 4 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20150108 MGI 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0004447 small basioccipital bone IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0008818 abnormal interfrontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0009899 hyoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312798 Wnt9a wingless-type MMTV integration site family, member 9A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16818445 1312800 Cerk ceramide kinase gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18292572 1312800 Cerk ceramide kinase gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18292572 1312800 Cerk ceramide kinase gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18292572 1312800 Cerk ceramide kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18292572 1312800 Cerk ceramide kinase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17888878 1312800 Cerk ceramide kinase gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18292572 1312800 Cerk ceramide kinase gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20141003 MGI PMID:17888878 1312800 Cerk ceramide kinase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18292572 1312800 Cerk ceramide kinase gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20160721 MGI PMID:18555012 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:17303760 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21989910 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:19631204 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21989910 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21989910 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17303760 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:17303760 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:21989910 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:21989910 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0006006 increased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:19631204 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:17303760 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20141003 MGI PMID:17303760 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:17303760 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:21989910 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:21989910 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0009410 abnormal skeletal muscle satellite cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21989910 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17303760 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:17303760 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:17303760 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17303760 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21989910 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20201022 MGI 1312806 Heyl hairy/enhancer-of-split related with YRPW motif-like gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:21989910 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:23122289 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0000380 small hair follicles IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:23122289 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0002223 lymphoid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23122289 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23122289 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23122289 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20210128 MGI 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:23122289 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:23122289 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:23122289 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23122289 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23122289 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:23122289 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:23122289 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:23122289 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23122289 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0010682 abnormal hair follicle infundibulum morphology IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0010684 abnormal hair follicle outer root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23122289 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21317239 1312814 Ezh1 enhancer of zeste 1 polycomb repressive complex 2 subunit gene MP:0011195 increased hair follicle apoptosis IAGP N RGD:5509061 20181129 MGI PMID:21317239 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:15004160 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:16301622 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:18375937 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15585875 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11672539 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16301622 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:18375937 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:15004160 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:19620301 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0004798 decreased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:16301622 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0004822 decreased susceptibility to experimental autoimmune uveoretinitis IAGP N RGD:5509061 20141003 MGI PMID:17118967 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15585875 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:11672539 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:15004160 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11672539 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:11672539 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:15585875 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:17118967 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:18375937 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:16301622 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:18375937 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:18375937 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15004160 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15004160 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11672539 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16301622 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17118967 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18375937 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:15004160 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:17118967 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:15004160 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:15004160 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:15004160 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008626 increased circulating interleukin-5 level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:15004160 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:18375937 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15004160 1312816 Il27ra interleukin 27 receptor, alpha gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15004160 1312822 Tmprss4 transmembrane protease, serine 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20161117 MGI PMID:26309024 1312824 Net1 neuroepithelial cell transforming gene 1 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20160225 MGI PMID:25321414 1312824 Net1 neuroepithelial cell transforming gene 1 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20160225 MGI PMID:25321414 1312824 Net1 neuroepithelial cell transforming gene 1 gene MP:0008904 abnormal mammary fat pad morphology IAGP N RGD:5509061 20160225 MGI PMID:25321414 1312824 Net1 neuroepithelial cell transforming gene 1 gene MP:0013784 abnormal mammary gland bud elongation IAGP N RGD:5509061 20160225 MGI PMID:25321414 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20201022 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20240523 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0003960 increased lean body mass IEA N RGD:5509061 20240523 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20240523 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220519 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0005505 thrombocytosis IEA N RGD:5509061 20240523 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20240523 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220519 MGI 1312826 Mmaa methylmalonic aciduria (cobalamin deficiency) type A gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220811 MGI 1312831 Icam5 intercellular adhesion molecule 5, telencephalin gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:11135016 1312831 Icam5 intercellular adhesion molecule 5, telencephalin gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20201022 MGI 1312831 Icam5 intercellular adhesion molecule 5, telencephalin gene MP:0002634 abnormal sensorimotor gating IAGP N RGD:5509061 20141003 MGI PMID:11135016 1312831 Icam5 intercellular adhesion molecule 5, telencephalin gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11135016 1312833 Six5 sine oculis-related homeobox 5 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:15163633 1312833 Six5 sine oculis-related homeobox 5 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15163633 1312833 Six5 sine oculis-related homeobox 5 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:15163633 1312833 Six5 sine oculis-related homeobox 5 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:15163633 1312833 Six5 sine oculis-related homeobox 5 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:15163633 1312833 Six5 sine oculis-related homeobox 5 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15163633 1312833 Six5 sine oculis-related homeobox 5 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:10802667 1312833 Six5 sine oculis-related homeobox 5 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:10802668 1312833 Six5 sine oculis-related homeobox 5 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15163633 1312833 Six5 sine oculis-related homeobox 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15163633 1312833 Six5 sine oculis-related homeobox 5 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15163633 1312833 Six5 sine oculis-related homeobox 5 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15163633 1312833 Six5 sine oculis-related homeobox 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:15163633 1312833 Six5 sine oculis-related homeobox 5 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20141003 MGI PMID:15163633 1312833 Six5 sine oculis-related homeobox 5 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:15163633 1312833 Six5 sine oculis-related homeobox 5 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:10802668 1312838 Zan zonadhesin gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20200102 MGI PMID:20529856 1312840 Emc7 ER membrane protein complex subunit 7 gene MP:0010166 increased response to stress-induced hyperthermia IEA N RGD:5509061 20170323 MGI 1312840 Emc7 ER membrane protein complex subunit 7 gene MP:0010770 preweaning lethality IEA N RGD:5509061 20170323 MGI 1312840 Emc7 ER membrane protein complex subunit 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1312842 Stk11ip serine/threonine kinase 11 interacting protein gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20221201 MGI PMID:33486894 1312842 Stk11ip serine/threonine kinase 11 interacting protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312842 Stk11ip serine/threonine kinase 11 interacting protein gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20210520 MGI 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20170504 MGI 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20160616 MGI PMID:25432536 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160616 MGI PMID:25432536 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20160616 MGI PMID:25432536 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20160616 MGI PMID:25432536 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20171228 MGI 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0003584 bifid ureter IEA N RGD:5509061 20171228 MGI 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0003586 dilated ureter IEA N RGD:5509061 20170504 MGI 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0004017 duplex kidney IEA N RGD:5509061 20171228 MGI 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20160616 MGI PMID:25432536 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:24357318 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:24357318 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:24357318 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20160616 MGI PMID:25432536 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0010484 bicuspid aortic valve IEA N RGD:5509061 20171228 MGI 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0010490 abnormal inferior vena cava valve morphology IEA N RGD:5509061 20170504 MGI 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160616 MGI PMID:25432536 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24357318 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1312846 Cyfip2 cytoplasmic FMR1 interacting protein 2 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:24357318 1312851 Pgs1 phosphatidylglycerophosphate synthase 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1312851 Pgs1 phosphatidylglycerophosphate synthase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312853 Arhgap18 Rho GTPase activating protein 18 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20160804 MGI 1312853 Arhgap18 Rho GTPase activating protein 18 gene MP:0001257 increased body length IEA N RGD:5509061 20160804 MGI 1312855 Dntt deoxynucleotidyltransferase, terminal gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:8356451 1312855 Dntt deoxynucleotidyltransferase, terminal gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10792495 1312855 Dntt deoxynucleotidyltransferase, terminal gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1312855 Dntt deoxynucleotidyltransferase, terminal gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8356452 1312855 Dntt deoxynucleotidyltransferase, terminal gene MP:0003063 increased coping response IEA N RGD:5509061 20211021 MGI 1312855 Dntt deoxynucleotidyltransferase, terminal gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:10607487 1312855 Dntt deoxynucleotidyltransferase, terminal gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1312855 Dntt deoxynucleotidyltransferase, terminal gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1312855 Dntt deoxynucleotidyltransferase, terminal gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10792495 1312855 Dntt deoxynucleotidyltransferase, terminal gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10792495 1312855 Dntt deoxynucleotidyltransferase, terminal gene MP:0008761 abnormal immunoglobulin light chain V-J recombination IAGP N RGD:5509061 20141003 MGI PMID:16860755 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0003031 acidosis IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0004119 hypokalemia IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0004410 absent endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0008309 dilated scala media IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0011625 cystolithiasis IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312857 Atp6v0a4 ATPase, H+ transporting, lysosomal V0 subunit A4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:22872862 1312860 Nagk N-acetylglucosamine kinase gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1312860 Nagk N-acetylglucosamine kinase gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1312860 Nagk N-acetylglucosamine kinase gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1312860 Nagk N-acetylglucosamine kinase gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 1312860 Nagk N-acetylglucosamine kinase gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1312862 Rab34 RAB34, member RAS oncogene family gene MP:0000111 cleft palate IEA N RGD:5509061 20210520 MGI 1312862 Rab34 RAB34, member RAS oncogene family gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20160811 MGI 1312862 Rab34 RAB34, member RAS oncogene family gene MP:0000562 polydactyly IEA N RGD:5509061 20210520 MGI 1312862 Rab34 RAB34, member RAS oncogene family gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1312862 Rab34 RAB34, member RAS oncogene family gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1312862 Rab34 RAB34, member RAS oncogene family gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20160421 MGI 1312862 Rab34 RAB34, member RAS oncogene family gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1312862 Rab34 RAB34, member RAS oncogene family gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20160811 MGI 1312862 Rab34 RAB34, member RAS oncogene family gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20160811 MGI 1312862 Rab34 RAB34, member RAS oncogene family gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20160421 MGI 1312862 Rab34 RAB34, member RAS oncogene family gene MP:0008797 facial cleft IEA N RGD:5509061 20210520 MGI 1312862 Rab34 RAB34, member RAS oncogene family gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312862 Rab34 RAB34, member RAS oncogene family gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1312864 Rbm5 RNA binding motif protein 5 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20160526 MGI PMID:23935508 1312864 Rbm5 RNA binding motif protein 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20160526 MGI PMID:23935508 1312864 Rbm5 RNA binding motif protein 5 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20160526 MGI PMID:23935508 1312864 Rbm5 RNA binding motif protein 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20160526 MGI PMID:23935508 1312864 Rbm5 RNA binding motif protein 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20160526 MGI PMID:23935508 1312864 Rbm5 RNA binding motif protein 5 gene MP:0006380 abnormal spermatid morphology IEA N RGD:5509061 20141003 MGI 1312864 Rbm5 RNA binding motif protein 5 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20160526 MGI PMID:23935508 1312864 Rbm5 RNA binding motif protein 5 gene MP:0008280 abnormal male germ cell apoptosis IEA N RGD:5509061 20141003 MGI 1312864 Rbm5 RNA binding motif protein 5 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20160526 MGI PMID:23935508 1312867 Tppp3 tubulin polymerization-promoting protein family member 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1312867 Tppp3 tubulin polymerization-promoting protein family member 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1312867 Tppp3 tubulin polymerization-promoting protein family member 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1312867 Tppp3 tubulin polymerization-promoting protein family member 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1312867 Tppp3 tubulin polymerization-promoting protein family member 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1312867 Tppp3 tubulin polymerization-promoting protein family member 3 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230601 MGI 1312867 Tppp3 tubulin polymerization-promoting protein family member 3 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1312867 Tppp3 tubulin polymerization-promoting protein family member 3 gene MP:0008039 increased NK T cell number IEA N RGD:5509061 20240523 MGI 1312867 Tppp3 tubulin polymerization-promoting protein family member 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1312867 Tppp3 tubulin polymerization-promoting protein family member 3 gene MP:0013129 abnormal tooth color IEA N RGD:5509061 20230601 MGI 1312867 Tppp3 tubulin polymerization-promoting protein family member 3 gene MP:0013520 increased CD4-positive NK T cell number IEA N RGD:5509061 20230601 MGI 1312867 Tppp3 tubulin polymerization-promoting protein family member 3 gene MP:0013523 increased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20230601 MGI 1312876 Tnfsf18 tumor necrosis factor (ligand) superfamily, member 18 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20240502 MGI PMID:38321001 1312876 Tnfsf18 tumor necrosis factor (ligand) superfamily, member 18 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20240502 MGI PMID:38321001 1312876 Tnfsf18 tumor necrosis factor (ligand) superfamily, member 18 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20211021 MGI 1312876 Tnfsf18 tumor necrosis factor (ligand) superfamily, member 18 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20240502 MGI PMID:38321001 1312876 Tnfsf18 tumor necrosis factor (ligand) superfamily, member 18 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1312876 Tnfsf18 tumor necrosis factor (ligand) superfamily, member 18 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20240502 MGI PMID:38321001 1312876 Tnfsf18 tumor necrosis factor (ligand) superfamily, member 18 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20240502 MGI PMID:38321001 1312876 Tnfsf18 tumor necrosis factor (ligand) superfamily, member 18 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20240502 MGI PMID:38321001 1312876 Tnfsf18 tumor necrosis factor (ligand) superfamily, member 18 gene MP:0012243 decreased hepatoblast number IAGP N RGD:5509061 20240502 MGI PMID:38321001 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160225 MGI PMID:25320092 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160225 MGI PMID:25320092 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20160225 MGI PMID:25320092 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0002673 abnormal sperm number IAGP N RGD:5509061 20160225 MGI PMID:25320092 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20160225 MGI PMID:25320092 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0005410 abnormal fertilization IAGP N RGD:5509061 20160225 MGI PMID:25320092 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20160225 MGI PMID:25320092 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20160225 MGI PMID:25320092 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20160225 MGI PMID:25320092 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20160225 MGI PMID:25320092 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20170105 MGI 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160225 MGI PMID:25320092 1312878 Ube2j1 ubiquitin-conjugating enzyme E2J 1 gene MP:0011941 increased fluid intake IEA N RGD:5509061 20211021 MGI 1312881 Smad6 SMAD family member 6 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20141003 MGI 1312881 Smad6 SMAD family member 6 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1312881 Smad6 SMAD family member 6 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0003958 heart valve hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0006123 tricuspid valve atresia IEA N RGD:5509061 20141003 MGI 1312881 Smad6 SMAD family member 6 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20141003 MGI 1312881 Smad6 SMAD family member 6 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20141003 MGI 1312881 Smad6 SMAD family member 6 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0011665 d-loop transposition of the great arteries IEA N RGD:5509061 20141003 MGI 1312881 Smad6 SMAD family member 6 gene MP:0031524 mitral valve hyperplasia IAGP N RGD:5509061 20240104 MGI PMID:10655064 1312881 Smad6 SMAD family member 6 gene MP:0031529 pulmonary valve hyperplasia IAGP N RGD:5509061 20240104 MGI PMID:10655064 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0000599 enlarged liver IEA N RGD:5509061 20210520 MGI 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20161103 MGI PMID:25118264 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0002698 abnormal sclera morphology IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0005098 abnormal optic choroid morphology IAGP N RGD:5509061 20161103 MGI PMID:25118264 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20161103 MGI PMID:25118264 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0006187 retina deposits IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20240208 MGI PMID:35230417 1312887 Cyp4v3 cytochrome P450, family 4, subfamily v, polypeptide 3 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:35230417 1312889 Trim69 tripartite motif-containing 69 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:33273151 1312889 Trim69 tripartite motif-containing 69 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210826 MGI 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0000410 waved hair IAGP N RGD:5509061 20200827 MGI PMID:32646486 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20161103 MGI PMID:25918388 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20200827 MGI PMID:32646486 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17218265 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17218265 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20161103 MGI PMID:25918388 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200820 MGI PMID:32646486 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25918388 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:17218265 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:17218265 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:17218265 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:17218265 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:17218265 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20161103 MGI PMID:25918388 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17218265 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:17218265 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0009154 pancreatic acinar hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0009162 absent pancreatic acinar cell zymogen granule IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20161103 MGI PMID:25918388 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0010591 enlarged aortic valve IAGP N RGD:5509061 20161103 MGI PMID:25918388 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20161103 MGI PMID:25918388 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0010600 enlarged pulmonary valve IAGP N RGD:5509061 20161103 MGI PMID:25918388 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0010605 thick pulmonary valve cusps IAGP N RGD:5509061 20161103 MGI PMID:25918388 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0010626 thick tricuspid valve cusps IAGP N RGD:5509061 20161103 MGI PMID:25918388 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0010627 enlarged tricuspid valve IAGP N RGD:5509061 20161103 MGI PMID:25918388 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17218265 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17218265 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17218265 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0011945 increased eating frequency IAGP N RGD:5509061 20141003 MGI PMID:23969955 1312891 Rhbdf1 rhomboid 5 homolog 1 gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20161124 MGI PMID:23969955 1312893 Cdc16 CDC16 cell division cycle 16 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312896 Sulf2 sulfatase 2 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17593974 1312896 Sulf2 sulfatase 2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:17593974 1312896 Sulf2 sulfatase 2 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22298771 1312896 Sulf2 sulfatase 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17720696 1312896 Sulf2 sulfatase 2 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17720696 1312896 Sulf2 sulfatase 2 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17720696 1312896 Sulf2 sulfatase 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17116694 1312896 Sulf2 sulfatase 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17593974 1312896 Sulf2 sulfatase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16901266 1312896 Sulf2 sulfatase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17116694 1312896 Sulf2 sulfatase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17593974 1312896 Sulf2 sulfatase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17720696 1312896 Sulf2 sulfatase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17116694 1312896 Sulf2 sulfatase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17720696 1312896 Sulf2 sulfatase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17720696 1312896 Sulf2 sulfatase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17116694 1312896 Sulf2 sulfatase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17720696 1312896 Sulf2 sulfatase 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:17720696 1312896 Sulf2 sulfatase 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17116694 1312896 Sulf2 sulfatase 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17116694 1312896 Sulf2 sulfatase 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:16901266 1312896 Sulf2 sulfatase 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17116694 1312896 Sulf2 sulfatase 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20210211 MGI PMID:17720696 1312896 Sulf2 sulfatase 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17593974 1312896 Sulf2 sulfatase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16901266 1312896 Sulf2 sulfatase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17593974 1312896 Sulf2 sulfatase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:16901266 1312896 Sulf2 sulfatase 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:17593974 1312896 Sulf2 sulfatase 2 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:17593974 1312896 Sulf2 sulfatase 2 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0004545 enlarged esophagus IAGP N RGD:5509061 20141003 MGI PMID:17720696 1312896 Sulf2 sulfatase 2 gene MP:0004548 dilated esophagus IAGP N RGD:5509061 20141003 MGI PMID:17720696 1312896 Sulf2 sulfatase 2 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0004622 sacral vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0004687 split vertebrae IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0004831 long incisors IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16901266 1312896 Sulf2 sulfatase 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17593974 1312896 Sulf2 sulfatase 2 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:17593974 1312896 Sulf2 sulfatase 2 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:17593974 1312896 Sulf2 sulfatase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17116694 1312896 Sulf2 sulfatase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17720696 1312896 Sulf2 sulfatase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22298771 1312896 Sulf2 sulfatase 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17593974 1312896 Sulf2 sulfatase 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17116694 1312896 Sulf2 sulfatase 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17116694 1312896 Sulf2 sulfatase 2 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:16901266 1312896 Sulf2 sulfatase 2 gene MP:0012279 wide sternum IAGP N RGD:5509061 20141003 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20180125 MGI PMID:18213582 1312896 Sulf2 sulfatase 2 gene MP:0031088 coughing IAGP N RGD:5509061 20210211 MGI PMID:17720696 1312898 Dse dermatan sulfate epimerase gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:19687302 1312898 Dse dermatan sulfate epimerase gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19687302 1312898 Dse dermatan sulfate epimerase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19687302 1312898 Dse dermatan sulfate epimerase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19687302 1312898 Dse dermatan sulfate epimerase gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:19687302 1312898 Dse dermatan sulfate epimerase gene MP:0003705 abnormal hypodermis morphology IAGP N RGD:5509061 20141003 MGI PMID:19687302 1312898 Dse dermatan sulfate epimerase gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1312898 Dse dermatan sulfate epimerase gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:19687302 1312898 Dse dermatan sulfate epimerase gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19687302 1312898 Dse dermatan sulfate epimerase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312902 Aif1l allograft inflammatory factor 1-like gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20160811 MGI 1312902 Aif1l allograft inflammatory factor 1-like gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20160811 MGI 1312902 Aif1l allograft inflammatory factor 1-like gene MP:0000691 enlarged spleen IEA N RGD:5509061 20160811 MGI 1312902 Aif1l allograft inflammatory factor 1-like gene MP:0000706 small thymus IEA N RGD:5509061 20160811 MGI 1312902 Aif1l allograft inflammatory factor 1-like gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20160811 MGI 1312902 Aif1l allograft inflammatory factor 1-like gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1312902 Aif1l allograft inflammatory factor 1-like gene MP:0004952 increased spleen weight IEA N RGD:5509061 20220811 MGI 1312908 Matn3 matrilin 3 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17517694 1312908 Matn3 matrilin 3 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17517694 1312908 Matn3 matrilin 3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1312908 Matn3 matrilin 3 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17517694 1312908 Matn3 matrilin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17517694 1312908 Matn3 matrilin 3 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:17517694 1312908 Matn3 matrilin 3 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:17517694 1312908 Matn3 matrilin 3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1312908 Matn3 matrilin 3 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17517694 1312908 Matn3 matrilin 3 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:16877353 1312908 Matn3 matrilin 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:16877353 1312908 Matn3 matrilin 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:17517694 1312908 Matn3 matrilin 3 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17517694 1312908 Matn3 matrilin 3 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1312908 Matn3 matrilin 3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1312908 Matn3 matrilin 3 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:16877353 1312908 Matn3 matrilin 3 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1312908 Matn3 matrilin 3 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20210812 MGI PMID:27573814 1312908 Matn3 matrilin 3 gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20210812 MGI PMID:27573814 1312908 Matn3 matrilin 3 gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:17517694 1312908 Matn3 matrilin 3 gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20171221 MGI PMID:17517694 1312910 Slc9b1 solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1312910 Slc9b1 solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1312910 Slc9b1 solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1312910 Slc9b1 solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 gene MP:0000599 enlarged liver IEA N RGD:5509061 20210520 MGI 1312910 Slc9b1 solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1312910 Slc9b1 solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1312910 Slc9b1 solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20201022 MGI 1312910 Slc9b1 solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 1312910 Slc9b1 solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1312910 Slc9b1 solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1312910 Slc9b1 solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20201022 MGI 1312910 Slc9b1 solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20240523 MGI 1312910 Slc9b1 solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1312914 Prorp protein only RNase P catalytic subunit gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20190919 MGI PMID:27498866 1312914 Prorp protein only RNase P catalytic subunit gene MP:0002083 premature death IAGP N RGD:5509061 20190919 MGI PMID:27498866 1312914 Prorp protein only RNase P catalytic subunit gene MP:0002833 increased heart weight IAGP N RGD:5509061 20190919 MGI PMID:27498866 1312914 Prorp protein only RNase P catalytic subunit gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20190919 MGI PMID:27498866 1312914 Prorp protein only RNase P catalytic subunit gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20190919 MGI PMID:27498866 1312914 Prorp protein only RNase P catalytic subunit gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20190919 MGI PMID:27498866 1312914 Prorp protein only RNase P catalytic subunit gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20190919 MGI PMID:27498866 1312914 Prorp protein only RNase P catalytic subunit gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20190919 MGI PMID:27498866 1312915 Sh3d21 SH3 domain containing 21 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240627 MGI PMID:38835510 1312917 Msrb1 methionine sulfoxide reductase B1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22521563 1312917 Msrb1 methionine sulfoxide reductase B1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22521563 1312917 Msrb1 methionine sulfoxide reductase B1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:18990697 1312920 Mxd4 Max dimerization protein 4 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20230601 MGI 1312920 Mxd4 Max dimerization protein 4 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20240523 MGI 1312920 Mxd4 Max dimerization protein 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1312920 Mxd4 Max dimerization protein 4 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20230601 MGI 1312923 Fbxo24 F-box protein 24 gene MP:0001925 male infertility IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0014468 disorganized sperm mitochondrial sheath IAGP N RGD:5509061 20240613 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20240523 MGI PMID:38470475 1312923 Fbxo24 F-box protein 24 gene MP:0031620 abnormal chromatoid body morphology IAGP N RGD:5509061 20240613 MGI PMID:38470475 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0002083 premature death IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0004697 abnormal thyroid follicular cell morphology IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0006350 increased circulating copper level IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0020365 increased brain iron level IAGP N RGD:5509061 20180614 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0030593 abnormal manganese level IAGP N RGD:5509061 20180621 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0030595 increased brain manganese level IAGP N RGD:5509061 20180621 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0030598 increased liver manganese level IAGP N RGD:5509061 20180621 MGI PMID:28461334 1312928 Slc30a10 solute carrier family 30, member 10 gene MP:0030601 increased circulating manganese level IAGP N RGD:5509061 20180621 MGI PMID:28461334 1312930 Rufy1 RUN and FYVE domain containing 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1312932 Lpar2 lysophosphatidic acid receptor 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:22427635 1312932 Lpar2 lysophosphatidic acid receptor 2 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:22427635 1312932 Lpar2 lysophosphatidic acid receptor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12215548 1312932 Lpar2 lysophosphatidic acid receptor 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22427635 1312932 Lpar2 lysophosphatidic acid receptor 2 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:22427635 1312932 Lpar2 lysophosphatidic acid receptor 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19766573 1312932 Lpar2 lysophosphatidic acid receptor 2 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:22427635 1312932 Lpar2 lysophosphatidic acid receptor 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22427635 1312932 Lpar2 lysophosphatidic acid receptor 2 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:22427635 1312932 Lpar2 lysophosphatidic acid receptor 2 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:22427635 1312932 Lpar2 lysophosphatidic acid receptor 2 gene MP:0010935 increased airway resistance IAGP N RGD:5509061 20141003 MGI PMID:22427635 1312936 Scel sciellin gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1312936 Scel sciellin gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1312936 Scel sciellin gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1312936 Scel sciellin gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1312936 Scel sciellin gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1312936 Scel sciellin gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1312936 Scel sciellin gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230601 MGI 1312936 Scel sciellin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16028229 1312936 Scel sciellin gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20230601 MGI 1312938 Csmd1 CUB and Sushi multiple domains 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:24244513 1312938 Csmd1 CUB and Sushi multiple domains 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:24244513 1312938 Csmd1 CUB and Sushi multiple domains 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:24244513 1312938 Csmd1 CUB and Sushi multiple domains 1 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:24244513 1312938 Csmd1 CUB and Sushi multiple domains 1 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:24244513 1312938 Csmd1 CUB and Sushi multiple domains 1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:24244513 1312938 Csmd1 CUB and Sushi multiple domains 1 gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20141003 MGI PMID:24244513 1312938 Csmd1 CUB and Sushi multiple domains 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:24244513 1312938 Csmd1 CUB and Sushi multiple domains 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20181227 MGI 1312938 Csmd1 CUB and Sushi multiple domains 1 gene MP:0010099 abnormal thoracic cage shape IEA N RGD:5509061 20181227 MGI 1312938 Csmd1 CUB and Sushi multiple domains 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:24244513 1312940 Ankrd2 ankyrin repeat domain 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141225 MGI PMID:24434510 1312940 Ankrd2 ankyrin repeat domain 2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141225 MGI PMID:24434510 1312940 Ankrd2 ankyrin repeat domain 2 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:17392382 1312940 Ankrd2 ankyrin repeat domain 2 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:17392382 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12910269 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0000371 diluted coat color IAGP N RGD:5509061 20150813 MGI PMID:24636991 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0000418 focal hair loss IAGP N RGD:5509061 20150813 MGI PMID:24636991 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0000676 abnormal body water content IAGP N RGD:5509061 20150813 MGI PMID:24636991 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0001212 skin lesions IAGP N RGD:5509061 20150813 MGI PMID:24636991 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0001258 decreased body length IEA N RGD:5509061 20190502 MGI 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210520 MGI 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0001314 cornea opacity IEA N RGD:5509061 20210520 MGI 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0001337 dry eyes IAGP N RGD:5509061 20150813 MGI PMID:24636991 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20150813 MGI PMID:24636991 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20150813 MGI PMID:24636991 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12910269 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12910269 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12910269 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0002992 abnormal sebaceous lipid secretion IAGP N RGD:5509061 20150813 MGI PMID:24636991 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20211021 MGI 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12910269 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:12910269 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20160414 MGI PMID:24636991 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0009935 abnormal Meibomian gland acinus morphology IAGP N RGD:5509061 20150813 MGI PMID:24636991 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0013116 focal hair loss in head/neck region IAGP N RGD:5509061 20150813 MGI PMID:24636991 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0013375 abnormal sebocyte morphology IAGP N RGD:5509061 20150813 MGI PMID:24636991 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0014053 dry hair IAGP N RGD:5509061 20160304 MGI PMID:24636991 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:12910269 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:12910269 1312943 Cidea cell death-inducing DNA fragmentation factor, alpha subunit-like effector A gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20180125 MGI PMID:12910269 1312945 Srpk2 serine/arginine-rich protein specific kinase 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20233966 1312945 Srpk2 serine/arginine-rich protein specific kinase 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20233966 1312945 Srpk2 serine/arginine-rich protein specific kinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20233966 1312945 Srpk2 serine/arginine-rich protein specific kinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20233966 1312945 Srpk2 serine/arginine-rich protein specific kinase 2 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20233966 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:23467409 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0000277 abnormal heart shape IEA N RGD:5509061 20210520 MGI 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:23467409 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210826 MGI 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221103 MGI 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23467409 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:23467409 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18084302 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:18084302 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23467409 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20221103 MGI 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23467409 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23467409 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19409815 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23467409 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23467409 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23467409 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23467409 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23467409 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:23467409 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0011702 abnormal fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:23467409 1312951 Arhgef12 Rho guanine nucleotide exchange factor 12 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:23467409 1312952 Tex2 testis expressed gene 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20240523 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20200514 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0004222 iris synechia IEA N RGD:5509061 20200514 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210128 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20240523 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20231207 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1312952 Tex2 testis expressed gene 2 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1312954 Nubp2 nucleotide binding protein 2 gene MP:0000087 absent mandible IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0000450 absent snout IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 1312954 Nubp2 nucleotide binding protein 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0008384 absent nasal capsule IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0008736 micromelia IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0008817 hematoma IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20210826 MGI 1312954 Nubp2 nucleotide binding protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312954 Nubp2 nucleotide binding protein 2 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0012260 encephalomeningocele IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0012522 abnormal stomodeum morphology IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0012761 increased cranial neural crest cell apoptosis IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0030202 nasal septum cartilage hypoplasia IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0030249 small frontonasal prominence IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0030342 small maxillary prominence IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0030344 absent maxillary prominence IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312954 Nubp2 nucleotide binding protein 2 gene MP:0030346 small mandibular prominence IAGP N RGD:5509061 20200917 MGI PMID:31733190 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0003547 abnormal pulmonary pressure IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0004009 abnormal diastolic filling velocity IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0004092 absent Z line IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0004093 diffuse Z line IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0004146 absent M line IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20180531 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20160421 MGI 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0010759 decreased right ventricle systolic pressure IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180503 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20170223 MGI PMID:21177343 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0030564 thick myocardium compact layer IAGP N RGD:5509061 20180524 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0030566 abnormal A band morphology IAGP N RGD:5509061 20180531 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0030567 abnormal I band morphology IAGP N RGD:5509061 20180531 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0030568 abnormal H zone morphology IAGP N RGD:5509061 20180531 MGI PMID:26526197 1312963 Daam1 dishevelled associated activator of morphogenesis 1 gene MP:0031613 fetal cardiomyocyte disarray IAGP N RGD:5509061 20240321 MGI PMID:21177343 1312968 Itpk1 inositol 1,3,4-triphosphate 5/6 kinase gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:19482943 1312968 Itpk1 inositol 1,3,4-triphosphate 5/6 kinase gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:19482943 1312968 Itpk1 inositol 1,3,4-triphosphate 5/6 kinase gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19482943 1312968 Itpk1 inositol 1,3,4-triphosphate 5/6 kinase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19482943 1312968 Itpk1 inositol 1,3,4-triphosphate 5/6 kinase gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:19482943 1312968 Itpk1 inositol 1,3,4-triphosphate 5/6 kinase gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:19482943 1312968 Itpk1 inositol 1,3,4-triphosphate 5/6 kinase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19482943 1312968 Itpk1 inositol 1,3,4-triphosphate 5/6 kinase gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:19482943 1312968 Itpk1 inositol 1,3,4-triphosphate 5/6 kinase gene MP:0009929 meningomyelocele IAGP N RGD:5509061 20141003 MGI PMID:19482943 1312968 Itpk1 inositol 1,3,4-triphosphate 5/6 kinase gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20150305 MGI PMID:19482943 1312970 Tbrg1 transforming growth factor beta regulated gene 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160324 MGI PMID:25393878 1312970 Tbrg1 transforming growth factor beta regulated gene 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20160324 MGI PMID:25393878 1312970 Tbrg1 transforming growth factor beta regulated gene 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20160324 MGI PMID:25393878 1312970 Tbrg1 transforming growth factor beta regulated gene 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20160324 MGI PMID:25393878 1312970 Tbrg1 transforming growth factor beta regulated gene 1 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20160324 MGI PMID:25393878 1312970 Tbrg1 transforming growth factor beta regulated gene 1 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20160324 MGI PMID:25393878 1312970 Tbrg1 transforming growth factor beta regulated gene 1 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20160324 MGI PMID:25393878 1312970 Tbrg1 transforming growth factor beta regulated gene 1 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20160324 MGI PMID:25393878 1312970 Tbrg1 transforming growth factor beta regulated gene 1 gene MP:0013329 abnormal preputial gland morphology IAGP N RGD:5509061 20160324 MGI PMID:25393878 1312970 Tbrg1 transforming growth factor beta regulated gene 1 gene MP:0013538 increased Harderian gland adenoma incidence IAGP N RGD:5509061 20160324 MGI PMID:25393878 1312972 Cilp cartilage intermediate layer protein, nucleotide pyrophosphohydrolase gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20201231 MGI 1312974 Atl2 atlastin GTPase 2 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20181227 MGI 1312974 Atl2 atlastin GTPase 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1312974 Atl2 atlastin GTPase 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1312974 Atl2 atlastin GTPase 2 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 1312974 Atl2 atlastin GTPase 2 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20170105 MGI 1312974 Atl2 atlastin GTPase 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20170105 MGI 1312974 Atl2 atlastin GTPase 2 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1312974 Atl2 atlastin GTPase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312974 Atl2 atlastin GTPase 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1312976 Kif21a kinesin family member 21A gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20181122 MGI PMID:24656932 1312976 Kif21a kinesin family member 21A gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20181122 MGI PMID:24656932 1312976 Kif21a kinesin family member 21A gene MP:0001061 abnormal oculomotor nerve morphology IAGP N RGD:5509061 20181122 MGI PMID:24656932 1312976 Kif21a kinesin family member 21A gene MP:0001070 abnormal abducens nerve morphology IAGP N RGD:5509061 20181122 MGI PMID:24656932 1312976 Kif21a kinesin family member 21A gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20181122 MGI PMID:24656932 1312976 Kif21a kinesin family member 21A gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20181122 MGI PMID:24656932 1312976 Kif21a kinesin family member 21A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20181122 MGI PMID:24656932 1312976 Kif21a kinesin family member 21A gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20181122 MGI PMID:24656932 1312976 Kif21a kinesin family member 21A gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20181122 MGI PMID:24656932 1312976 Kif21a kinesin family member 21A gene MP:0005247 abnormal extraocular muscle morphology IAGP N RGD:5509061 20181122 MGI PMID:24656932 1312976 Kif21a kinesin family member 21A gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20181122 MGI PMID:24656932 1312976 Kif21a kinesin family member 21A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20181122 MGI PMID:24656932 1312976 Kif21a kinesin family member 21A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312976 Kif21a kinesin family member 21A gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20200402 MGI 1312976 Kif21a kinesin family member 21A gene MP:0013827 thin oculomotor nerve IAGP N RGD:5509061 20181122 MGI PMID:24656932 1312979 Polg2 polymerase (DNA directed), gamma 2, accessory subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23197651 1312979 Polg2 polymerase (DNA directed), gamma 2, accessory subunit gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20191114 MGI PMID:30395686 1312979 Polg2 polymerase (DNA directed), gamma 2, accessory subunit gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:23197651 1312979 Polg2 polymerase (DNA directed), gamma 2, accessory subunit gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:23197651 1312979 Polg2 polymerase (DNA directed), gamma 2, accessory subunit gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:23197651 1312979 Polg2 polymerase (DNA directed), gamma 2, accessory subunit gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23197651 1312979 Polg2 polymerase (DNA directed), gamma 2, accessory subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312979 Polg2 polymerase (DNA directed), gamma 2, accessory subunit gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20141003 MGI PMID:23197651 1312979 Polg2 polymerase (DNA directed), gamma 2, accessory subunit gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20141003 MGI PMID:23197651 1312985 Twf2 twinfilin actin binding protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21876732 1312989 Slc25a28 solute carrier family 25, member 28 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201231 MGI 1312989 Slc25a28 solute carrier family 25, member 28 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210415 MGI PMID:32518166 1312989 Slc25a28 solute carrier family 25, member 28 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210415 MGI PMID:32518166 1312989 Slc25a28 solute carrier family 25, member 28 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210415 MGI PMID:32518166 1312989 Slc25a28 solute carrier family 25, member 28 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20210415 MGI PMID:32518166 1312989 Slc25a28 solute carrier family 25, member 28 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20210415 MGI PMID:32518166 1312989 Slc25a28 solute carrier family 25, member 28 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20210415 MGI PMID:32518166 1312997 Zfp281 zinc finger protein 281 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1312997 Zfp281 zinc finger protein 281 gene MP:0000692 small spleen IEA N RGD:5509061 20201022 MGI 1312997 Zfp281 zinc finger protein 281 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20231207 MGI 1312997 Zfp281 zinc finger protein 281 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1312997 Zfp281 zinc finger protein 281 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1312997 Zfp281 zinc finger protein 281 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 1312997 Zfp281 zinc finger protein 281 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21915945 1312997 Zfp281 zinc finger protein 281 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21915945 1312997 Zfp281 zinc finger protein 281 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1312997 Zfp281 zinc finger protein 281 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1312997 Zfp281 zinc finger protein 281 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15060135 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17550782 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:17550782 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15060135 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15060135 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15060135 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15060135 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:17550782 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:15060135 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15060135 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0003364 increased insulinoma incidence IAGP N RGD:5509061 20170406 MGI PMID:18846252 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:15060135 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20170406 MGI PMID:18846252 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:17550782 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:17550782 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20150611 MGI PMID:17550782 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:17550782 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15060135 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15060135 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15060135 1313004 Rps6kb2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0014173 increased fatty acid beta-oxidation IAGP N RGD:5509061 20160421 MGI PMID:17550782 1313005 Nars2 asparaginyl-tRNA synthetase 2 (mitochondrial)(putative) gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1313005 Nars2 asparaginyl-tRNA synthetase 2 (mitochondrial)(putative) gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20181227 MGI 1313005 Nars2 asparaginyl-tRNA synthetase 2 (mitochondrial)(putative) gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191205 MGI 1313005 Nars2 asparaginyl-tRNA synthetase 2 (mitochondrial)(putative) gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1313005 Nars2 asparaginyl-tRNA synthetase 2 (mitochondrial)(putative) gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191205 MGI 1313005 Nars2 asparaginyl-tRNA synthetase 2 (mitochondrial)(putative) gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1313005 Nars2 asparaginyl-tRNA synthetase 2 (mitochondrial)(putative) gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 1313005 Nars2 asparaginyl-tRNA synthetase 2 (mitochondrial)(putative) gene MP:0009331 absent primitive node IEA N RGD:5509061 20191205 MGI 1313005 Nars2 asparaginyl-tRNA synthetase 2 (mitochondrial)(putative) gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1313005 Nars2 asparaginyl-tRNA synthetase 2 (mitochondrial)(putative) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313005 Nars2 asparaginyl-tRNA synthetase 2 (mitochondrial)(putative) gene MP:0012724 absent head fold IEA N RGD:5509061 20191205 MGI 1313005 Nars2 asparaginyl-tRNA synthetase 2 (mitochondrial)(putative) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191205 MGI 1313005 Nars2 asparaginyl-tRNA synthetase 2 (mitochondrial)(putative) gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1313007 Pcnx4 pecanex homolog 4 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1313007 Pcnx4 pecanex homolog 4 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:19913445 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:15322176 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:11777964 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18796634 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:19913445 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:18796634 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15322176 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18796634 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15322176 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0006412 abnormal T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11777964 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:11777964 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:18796634 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:11777964 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:14607906 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:18796634 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19913445 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:11777964 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18796634 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19913445 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19913445 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11777964 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11777964 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18796634 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19913445 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11777964 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11777964 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008363 decreased CD8-positive, gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:19913445 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:15322176 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11777964 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14607906 1313010 Il15ra interleukin 15 receptor, alpha chain gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19913445 1313013 B3gnt3 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 gene MP:0003998 decreased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 1313015 Itga10 integrin, alpha 10 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:15713743 1313015 Itga10 integrin, alpha 10 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:15713743 1313015 Itga10 integrin, alpha 10 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:15713743 1313015 Itga10 integrin, alpha 10 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:15713743 1313015 Itga10 integrin, alpha 10 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15713743 1313019 Adamtsl3 ADAMTS-like 3 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1313019 Adamtsl3 ADAMTS-like 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20220519 MGI 1313019 Adamtsl3 ADAMTS-like 3 gene MP:0000692 small spleen IEA N RGD:5509061 20210826 MGI 1313019 Adamtsl3 ADAMTS-like 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1313019 Adamtsl3 ADAMTS-like 3 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20220519 MGI 1313019 Adamtsl3 ADAMTS-like 3 gene MP:0002637 small uterus IEA N RGD:5509061 20220519 MGI 1313019 Adamtsl3 ADAMTS-like 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20230202 MGI PMID:36539599 1313019 Adamtsl3 ADAMTS-like 3 gene MP:0004357 long tibia IAGP N RGD:5509061 20230202 MGI PMID:36539599 1313019 Adamtsl3 ADAMTS-like 3 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20230202 MGI PMID:36539599 1313019 Adamtsl3 ADAMTS-like 3 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210826 MGI 1313026 Atpaf2 ATP synthase mitochondrial F1 complex assembly factor 2 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20141003 MGI 1313026 Atpaf2 ATP synthase mitochondrial F1 complex assembly factor 2 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20160804 MGI 1313026 Atpaf2 ATP synthase mitochondrial F1 complex assembly factor 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1313026 Atpaf2 ATP synthase mitochondrial F1 complex assembly factor 2 gene MP:0003345 decreased rib number IEA N RGD:5509061 20160804 MGI 1313026 Atpaf2 ATP synthase mitochondrial F1 complex assembly factor 2 gene MP:0004648 decreased thoracic vertebrae number IEA N RGD:5509061 20160804 MGI 1313026 Atpaf2 ATP synthase mitochondrial F1 complex assembly factor 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313034 Tctn3 tectonic family member 3 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1313034 Tctn3 tectonic family member 3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20191003 MGI PMID:28800946 1313034 Tctn3 tectonic family member 3 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20191003 MGI PMID:28800946 1313034 Tctn3 tectonic family member 3 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1313034 Tctn3 tectonic family member 3 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1313034 Tctn3 tectonic family member 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1313034 Tctn3 tectonic family member 3 gene MP:0001785 edema IAGP N RGD:5509061 20191003 MGI PMID:28800946 1313034 Tctn3 tectonic family member 3 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20201022 MGI 1313034 Tctn3 tectonic family member 3 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20191003 MGI PMID:28800946 1313034 Tctn3 tectonic family member 3 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20191003 MGI PMID:28800946 1313034 Tctn3 tectonic family member 3 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20220811 MGI 1313034 Tctn3 tectonic family member 3 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1313034 Tctn3 tectonic family member 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20191003 MGI PMID:28800946 1313034 Tctn3 tectonic family member 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20191003 MGI PMID:28800946 1313034 Tctn3 tectonic family member 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313034 Tctn3 tectonic family member 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20191003 MGI PMID:28800946 1313034 Tctn3 tectonic family member 3 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20191003 MGI PMID:28800946 1313034 Tctn3 tectonic family member 3 gene MP:0013214 decreased embryonic neuroepithelium primary cilium number IAGP N RGD:5509061 20191003 MGI PMID:28800946 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20210520 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0001314 cornea opacity IEA N RGD:5509061 20220811 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0002626 increased heart rate IEA N RGD:5509061 20210826 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210520 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210826 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1313035 Fsd2 fibronectin type III and SPRY domain containing 2 gene MP:0010507 shortened RR interval IEA N RGD:5509061 20210826 MGI 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0002083 premature death IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0003717 pallor IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0011243 decreased fetal derived definitive erythrocyte cell number IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0011903 decreased hematopoietic stem cell proliferation IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0011913 abnormal reticulocyte cell number IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20170907 MGI PMID:26456157 1313037 Mcm3 minichromosome maintenance complex component 3 gene MP:0021086 decreased DNA replication IAGP N RGD:5509061 20220310 MGI PMID:26456157 1313039 Pank2 pantothenate kinase 2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20231207 MGI 1313039 Pank2 pantothenate kinase 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20231207 MGI 1313039 Pank2 pantothenate kinase 2 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20231207 MGI 1313039 Pank2 pantothenate kinase 2 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20231207 MGI 1313039 Pank2 pantothenate kinase 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15525657 1313039 Pank2 pantothenate kinase 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15525657 1313039 Pank2 pantothenate kinase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15525657 1313039 Pank2 pantothenate kinase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15525657 1313039 Pank2 pantothenate kinase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1313039 Pank2 pantothenate kinase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15525657 1313039 Pank2 pantothenate kinase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15525657 1313039 Pank2 pantothenate kinase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0001926 female infertility IEA N RGD:5509061 20231207 MGI 1313039 Pank2 pantothenate kinase 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15525657 1313039 Pank2 pantothenate kinase 2 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20231207 MGI 1313039 Pank2 pantothenate kinase 2 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0002638 abnormal pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:15525657 1313039 Pank2 pantothenate kinase 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15525657 1313039 Pank2 pantothenate kinase 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 1313039 Pank2 pantothenate kinase 2 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:15525657 1313039 Pank2 pantothenate kinase 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0005387 immune system phenotype IEA N RGD:5509061 20231207 MGI 1313039 Pank2 pantothenate kinase 2 gene MP:0008455 abnormal retina rod cell inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15525657 1313039 Pank2 pantothenate kinase 2 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15525657 1313039 Pank2 pantothenate kinase 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20231207 MGI 1313039 Pank2 pantothenate kinase 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:22815849 1313039 Pank2 pantothenate kinase 2 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1313039 Pank2 pantothenate kinase 2 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:15525657 1313048 Magoh mago homolog, exon junction complex core component gene MP:0000373 belly spot IAGP N RGD:5509061 20151126 MGI PMID:24771530 1313048 Magoh mago homolog, exon junction complex core component gene MP:0000433 microcephaly IAGP N RGD:5509061 20200102 MGI PMID:27618312 1313048 Magoh mago homolog, exon junction complex core component gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:20364144 1313048 Magoh mago homolog, exon junction complex core component gene MP:0000774 decreased brain size IAGP N RGD:5509061 20151126 MGI PMID:24771530 1313048 Magoh mago homolog, exon junction complex core component gene MP:0000774 decreased brain size IAGP N RGD:5509061 20170511 MGI PMID:27780844 1313048 Magoh mago homolog, exon junction complex core component gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:20364144 1313048 Magoh mago homolog, exon junction complex core component gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20364144 1313048 Magoh mago homolog, exon junction complex core component gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151203 MGI PMID:24771530 1313048 Magoh mago homolog, exon junction complex core component gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20364144 1313048 Magoh mago homolog, exon junction complex core component gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20170511 MGI PMID:27780844 1313048 Magoh mago homolog, exon junction complex core component gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:20364144 1313048 Magoh mago homolog, exon junction complex core component gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20151126 MGI PMID:24771530 1313048 Magoh mago homolog, exon junction complex core component gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20151126 MGI PMID:24771530 1313048 Magoh mago homolog, exon junction complex core component gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:20364144 1313048 Magoh mago homolog, exon junction complex core component gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:20364144 1313048 Magoh mago homolog, exon junction complex core component gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:20364144 1313048 Magoh mago homolog, exon junction complex core component gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:20364144 1313048 Magoh mago homolog, exon junction complex core component gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20364144 1313048 Magoh mago homolog, exon junction complex core component gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20364144 1313048 Magoh mago homolog, exon junction complex core component gene MP:0011724 ectopic cortical neuron IAGP N RGD:5509061 20170511 MGI PMID:27780844 1313048 Magoh mago homolog, exon junction complex core component gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20170511 MGI PMID:27780844 1313048 Magoh mago homolog, exon junction complex core component gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20170511 MGI PMID:27780844 1313048 Magoh mago homolog, exon junction complex core component gene MP:0020069 decreased neocortex size IAGP N RGD:5509061 20170511 MGI PMID:27780844 1313049 Dcaf1 DDB1 and CUL4 associated factor 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18606781 1313049 Dcaf1 DDB1 and CUL4 associated factor 1 gene MP:0006204 embryonic lethality before implantation IEA N RGD:5509061 20111116 MGI 1313049 Dcaf1 DDB1 and CUL4 associated factor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18606781 1313049 Dcaf1 DDB1 and CUL4 associated factor 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20150212 MGI PMID:18606781 1313049 Dcaf1 DDB1 and CUL4 associated factor 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:18606781 1313050 Lctl lactase-like gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20190207 MGI PMID:29425878 1313050 Lctl lactase-like gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170406 MGI 1313050 Lctl lactase-like gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20190207 MGI PMID:29425878 1313050 Lctl lactase-like gene MP:0010255 cortical cataract IAGP N RGD:5509061 20190207 MGI PMID:29425878 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0001193 psoriasis IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313053 N4bp1 NEDD4 binding protein 1 gene MP:0013022 increased Ly6C high monocyte number IAGP N RGD:5509061 20210128 MGI PMID:32971525 1313055 Pbxip1 pre B cell leukemia transcription factor interacting protein 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20191024 MGI PMID:30659184 1313055 Pbxip1 pre B cell leukemia transcription factor interacting protein 1 gene MP:0003109 short femur IAGP N RGD:5509061 20191024 MGI PMID:30659184 1313055 Pbxip1 pre B cell leukemia transcription factor interacting protein 1 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20191024 MGI PMID:30659184 1313055 Pbxip1 pre B cell leukemia transcription factor interacting protein 1 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20191024 MGI PMID:30659184 1313055 Pbxip1 pre B cell leukemia transcription factor interacting protein 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20191024 MGI PMID:30659184 1313055 Pbxip1 pre B cell leukemia transcription factor interacting protein 1 gene MP:0004351 short humerus IAGP N RGD:5509061 20191024 MGI PMID:30659184 1313055 Pbxip1 pre B cell leukemia transcription factor interacting protein 1 gene MP:0004355 short radius IAGP N RGD:5509061 20191024 MGI PMID:30659184 1313055 Pbxip1 pre B cell leukemia transcription factor interacting protein 1 gene MP:0004359 short ulna IAGP N RGD:5509061 20191024 MGI PMID:30659184 1313055 Pbxip1 pre B cell leukemia transcription factor interacting protein 1 gene MP:0004708 short lumbar vertebrae IAGP N RGD:5509061 20191024 MGI PMID:30659184 1313055 Pbxip1 pre B cell leukemia transcription factor interacting protein 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20191024 MGI PMID:30659184 1313055 Pbxip1 pre B cell leukemia transcription factor interacting protein 1 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20191024 MGI PMID:30659184 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15987682 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15987682 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:15987682 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15987682 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0001400 hyperresponsive IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15987682 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:15987682 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0001513 limb grasping IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0001525 impaired balance IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15987682 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15987682 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180809 MGI PMID:28429368 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:15987682 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20180809 MGI PMID:28429368 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:15987682 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180809 MGI PMID:15987682 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180809 MGI PMID:28429368 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0030585 enhanced behavioral response to amphetamine IAGP N RGD:5509061 20180809 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0030635 increased taurine level IAGP N RGD:5509061 20180913 MGI PMID:28429368 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0030733 decreased gamma-aminobutyric acid level IAGP N RGD:5509061 20180927 MGI PMID:23216354 1313057 Slc25a12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:23216354 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:19578028 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:16051690 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:19578028 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0004284 abnormal Descemet membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16051690 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0004284 abnormal Descemet membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:22002996 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0004284 abnormal Descemet membrane morphology IAGP N RGD:5509061 20161013 MGI PMID:23422828 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16051690 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:16051690 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:19578028 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16051690 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22002996 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20161013 MGI PMID:23422828 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:16051690 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:19578028 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19578028 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:22002996 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22002996 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20161013 MGI PMID:23422828 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:22002996 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20161013 MGI PMID:23422828 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0009829 enlarged eye anterior chamber IAGP N RGD:5509061 20141003 MGI PMID:19578028 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0031177 decreased Descemet membrane thickness IAGP N RGD:5509061 20201119 MGI PMID:16051690 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0031177 decreased Descemet membrane thickness IAGP N RGD:5509061 20201119 MGI PMID:19578028 1313059 Col8a2 collagen, type VIII, alpha 2 gene MP:0031213 increased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:16051690 1313061 Cep76 centrosomal protein 76 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20161201 MGI 1313065 Ubap1 ubiquitin-associated protein 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20230119 MGI PMID:35962060 1313065 Ubap1 ubiquitin-associated protein 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20230119 MGI PMID:35962060 1313065 Ubap1 ubiquitin-associated protein 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20230119 MGI PMID:35962060 1313065 Ubap1 ubiquitin-associated protein 1 gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20230119 MGI PMID:35962060 1313065 Ubap1 ubiquitin-associated protein 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20230119 MGI PMID:35962060 1313065 Ubap1 ubiquitin-associated protein 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230119 MGI PMID:35962060 1313065 Ubap1 ubiquitin-associated protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313065 Ubap1 ubiquitin-associated protein 1 gene MP:0012051 spasticity IAGP N RGD:5509061 20230119 MGI PMID:35962060 1313065 Ubap1 ubiquitin-associated protein 1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20230119 MGI PMID:35962060 1313065 Ubap1 ubiquitin-associated protein 1 gene MP:0031204 hindlimb paresis IAGP N RGD:5509061 20230119 MGI PMID:35962060 1313073 Kifap3 kinesin-associated protein 3 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15834408 1313073 Kifap3 kinesin-associated protein 3 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:15834408 1313073 Kifap3 kinesin-associated protein 3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15834408 1313073 Kifap3 kinesin-associated protein 3 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15834408 1313073 Kifap3 kinesin-associated protein 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15834408 1313073 Kifap3 kinesin-associated protein 3 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:15834408 1313073 Kifap3 kinesin-associated protein 3 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1313073 Kifap3 kinesin-associated protein 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15834408 1313073 Kifap3 kinesin-associated protein 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313075 Sema7a sema domain, immunoglobulin domain (Ig), and GPI membrane anchor, (semaphorin) 7A gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:12879062 1313075 Sema7a sema domain, immunoglobulin domain (Ig), and GPI membrane anchor, (semaphorin) 7A gene MP:0005237 abnormal olfactory tract morphology IAGP N RGD:5509061 20141003 MGI PMID:12879062 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:1934076 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:7059672 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:14451913 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:7059672 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:7059672 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:7059672 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000314 schistocytosis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000314 schistocytosis IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:7059672 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000422 delayed hair appearance IEA N RGD:5509061 20111116 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:14451913 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:14451913 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:14451913 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:11154235 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:14451913 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:7059672 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11154235 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7059672 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001386 abnormal maternal nurturing IEA N RGD:5509061 20111116 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20200514 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11154235 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:14451913 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:1934076 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:7059672 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001923 reduced female fertility IEA N RGD:5509061 20111116 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002082 postnatal lethality IEA N RGD:5509061 20111116 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002095 abnormal skin pigmentation IEA N RGD:5509061 20111116 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002161 abnormal fertility/fecundity IEA N RGD:5509061 20111116 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002397 abnormal bone marrow morphology IEA N RGD:5509061 20111116 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002424 abnormal reticulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:6234993 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10772878 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:6234993 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20111116 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:7059672 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:14451913 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002704 tubular nephritis IAGP N RGD:5509061 20141003 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002810 microcytic anemia IEA N RGD:5509061 20111116 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:14451913 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:7059672 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:10772878 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:7059672 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002830 gallstones IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:14451913 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:11154235 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:7059672 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:7492791 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0003657 abnormal erythrocyte osmotic lysis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:14451913 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0003868 abnormal feces composition IEA N RGD:5509061 20111116 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0003946 renal necrosis IAGP N RGD:5509061 20141003 MGI PMID:11154235 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:1934076 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:1934076 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:1934076 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:1832936 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005096 erythroblastosis IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:1934076 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:14451913 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:1934076 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1934076 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1934076 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:1934076 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0008388 hypochromic microcytic anemia IEA N RGD:5509061 20111116 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:1934076 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:1934076 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0008956 decreased cellular hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0009547 elliptocytosis IAGP N RGD:5509061 20141003 MGI PMID:10772878 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0009547 elliptocytosis IAGP N RGD:5509061 20141003 MGI PMID:11154235 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0009547 elliptocytosis IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0009568 abnormal red blood cell deformability IAGP N RGD:5509061 20141003 MGI PMID:12393645 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:14451913 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0010035 increased erythrocyte clearance IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0010163 hemolysis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20141003 MGI PMID:20056793 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20141003 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0010922 alveolitis IAGP N RGD:5509061 20141003 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0011085 postnatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6841965 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14451913 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0011088 neonatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0011188 increased erythrocyte protoporphyrin level IAGP N RGD:5509061 20141003 MGI PMID:1832936 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0011188 increased erythrocyte protoporphyrin level IAGP N RGD:5509061 20141003 MGI PMID:658175 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0011188 increased erythrocyte protoporphyrin level IAGP N RGD:5509061 20141003 MGI PMID:7059672 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0014473 increased pulmonary alveolus wall thickness IAGP N RGD:5509061 20240704 MGI PMID:8355480 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20161124 MGI PMID:10772878 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20161124 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0021002 brain lesion IAGP N RGD:5509061 20210805 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0021003 cerebral infarct IAGP N RGD:5509061 20210805 MGI PMID:9373273 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:6763106 1313078 Spta1 spectrin alpha, erythrocytic 1 gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:6841965 1313082 Jph2 junctophilin 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10949023 1313082 Jph2 junctophilin 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:10949023 1313082 Jph2 junctophilin 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:10949023 1313082 Jph2 junctophilin 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10949023 1313084 Nrl neural retina leucine zipper gene gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:11694879 1313084 Nrl neural retina leucine zipper gene gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:12853434 1313084 Nrl neural retina leucine zipper gene gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:23319618 1313084 Nrl neural retina leucine zipper gene gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20161124 MGI PMID:21659555 1313084 Nrl neural retina leucine zipper gene gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20161124 MGI PMID:21659555 1313084 Nrl neural retina leucine zipper gene gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20161124 MGI PMID:21659555 1313084 Nrl neural retina leucine zipper gene gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:11694879 1313084 Nrl neural retina leucine zipper gene gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20161124 MGI PMID:21659555 1313084 Nrl neural retina leucine zipper gene gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11694879 1313084 Nrl neural retina leucine zipper gene gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21813673 1313084 Nrl neural retina leucine zipper gene gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11694879 1313084 Nrl neural retina leucine zipper gene gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21813673 1313084 Nrl neural retina leucine zipper gene gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23319618 1313084 Nrl neural retina leucine zipper gene gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11694879 1313084 Nrl neural retina leucine zipper gene gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21245082 1313084 Nrl neural retina leucine zipper gene gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23319618 1313084 Nrl neural retina leucine zipper gene gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20161124 MGI PMID:21659555 1313084 Nrl neural retina leucine zipper gene gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:21813673 1313084 Nrl neural retina leucine zipper gene gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:23319618 1313084 Nrl neural retina leucine zipper gene gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20161124 MGI PMID:21659555 1313084 Nrl neural retina leucine zipper gene gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180201 MGI PMID:26247368 1313084 Nrl neural retina leucine zipper gene gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20180201 MGI PMID:26247368 1313084 Nrl neural retina leucine zipper gene gene MP:0008445 increased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:21813673 1313084 Nrl neural retina leucine zipper gene gene MP:0008445 increased retina cone cell number IAGP N RGD:5509061 20161124 MGI PMID:21659555 1313084 Nrl neural retina leucine zipper gene gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20191003 MGI PMID:30228185 1313084 Nrl neural retina leucine zipper gene gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21245082 1313084 Nrl neural retina leucine zipper gene gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20161124 MGI PMID:21659555 1313084 Nrl neural retina leucine zipper gene gene MP:0008454 absent retina rod cells IAGP N RGD:5509061 20141003 MGI PMID:21813673 1313084 Nrl neural retina leucine zipper gene gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20180201 MGI PMID:26247368 1313084 Nrl neural retina leucine zipper gene gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:21813673 1313084 Nrl neural retina leucine zipper gene gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20180201 MGI PMID:26247368 1313084 Nrl neural retina leucine zipper gene gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20180201 MGI PMID:26247368 1313090 Ccm2l cerebral cavernous malformation 2-like gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22898778 1313090 Ccm2l cerebral cavernous malformation 2-like gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22898778 1313090 Ccm2l cerebral cavernous malformation 2-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22898778 1313090 Ccm2l cerebral cavernous malformation 2-like gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:22898778 1313090 Ccm2l cerebral cavernous malformation 2-like gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:22898778 1313090 Ccm2l cerebral cavernous malformation 2-like gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:22898778 1313090 Ccm2l cerebral cavernous malformation 2-like gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:22898778 1313090 Ccm2l cerebral cavernous malformation 2-like gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22898778 1313090 Ccm2l cerebral cavernous malformation 2-like gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22898778 1313090 Ccm2l cerebral cavernous malformation 2-like gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:22898778 1313090 Ccm2l cerebral cavernous malformation 2-like gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22898778 1313090 Ccm2l cerebral cavernous malformation 2-like gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22898778 1313090 Ccm2l cerebral cavernous malformation 2-like gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22898778 1313090 Ccm2l cerebral cavernous malformation 2-like gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:22898778 1313092 Bag1 BCL2-associated athanogene 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15560850 1313092 Bag1 BCL2-associated athanogene 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1313092 Bag1 BCL2-associated athanogene 1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160804 MGI 1313092 Bag1 BCL2-associated athanogene 1 gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15560850 1313092 Bag1 BCL2-associated athanogene 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15560850 1313096 Ipo4 importin 4 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210128 MGI 1313096 Ipo4 importin 4 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1313096 Ipo4 importin 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1313100 Ldlrad4 low density lipoprotein receptor class A domain containing 4 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20201231 MGI 1313100 Ldlrad4 low density lipoprotein receptor class A domain containing 4 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1313102 Lipt2 lipoyl(octanoyl) transferase 2 (putative) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1313104 Poli polymerase (DNA directed), iota gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:17015482 1313104 Poli polymerase (DNA directed), iota gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15824086 1313104 Poli polymerase (DNA directed), iota gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23955086 1313104 Poli polymerase (DNA directed), iota gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23955086 1313104 Poli polymerase (DNA directed), iota gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1313106 Pnn pinin gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19892877 1313106 Pnn pinin gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:19892877 1313106 Pnn pinin gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:19892877 1313106 Pnn pinin gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20141003 MGI PMID:19892877 1313106 Pnn pinin gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:19892877 1313106 Pnn pinin gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17654715 1313106 Pnn pinin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160211 MGI 1313106 Pnn pinin gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313106 Pnn pinin gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1313109 Usb1 U6 snRNA biogenesis 1 gene MP:0001785 edema IEA N RGD:5509061 20221215 MGI 1313109 Usb1 U6 snRNA biogenesis 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313109 Usb1 U6 snRNA biogenesis 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1313111 Sirt6 sirtuin 6 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20816089 1313111 Sirt6 sirtuin 6 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0001258 decreased body length IAGP N RGD:5509061 20160310 MGI PMID:26629408 1313111 Sirt6 sirtuin 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160310 MGI PMID:26629408 1313111 Sirt6 sirtuin 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0001316 cornea scarring IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0002083 premature death IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:20816089 1313111 Sirt6 sirtuin 6 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20816089 1313111 Sirt6 sirtuin 6 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20141003 MGI 1313111 Sirt6 sirtuin 6 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20816089 1313111 Sirt6 sirtuin 6 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 1313111 Sirt6 sirtuin 6 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0008402 increased cellular sensitivity to alkylating agents IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0008737 abnormal spleen physiology IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0020860 abnormal cornea physiology IAGP N RGD:5509061 20200116 MGI PMID:28448551 1313111 Sirt6 sirtuin 6 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:16439206 1313111 Sirt6 sirtuin 6 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:20847051 1313111 Sirt6 sirtuin 6 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:28448551 1313113 Foxb1 forkhead box B1 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11170346 1313113 Foxb1 forkhead box B1 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:15654859 1313113 Foxb1 forkhead box B1 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0000867 abnormal cerebellum anterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:9118797 1313113 Foxb1 forkhead box B1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9118797 1313113 Foxb1 forkhead box B1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9136764 1313113 Foxb1 forkhead box B1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:9136764 1313113 Foxb1 forkhead box B1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9136764 1313113 Foxb1 forkhead box B1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9136764 1313113 Foxb1 forkhead box B1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15654859 1313113 Foxb1 forkhead box B1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:9118797 1313113 Foxb1 forkhead box B1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:9136764 1313113 Foxb1 forkhead box B1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9118797 1313113 Foxb1 forkhead box B1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9136764 1313113 Foxb1 forkhead box B1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10662642 1313113 Foxb1 forkhead box B1 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:9118797 1313113 Foxb1 forkhead box B1 gene MP:0004162 abnormal mammillary body morphology IAGP N RGD:5509061 20141003 MGI PMID:11170346 1313113 Foxb1 forkhead box B1 gene MP:0004162 abnormal mammillary body morphology IAGP N RGD:5509061 20141003 MGI PMID:15654859 1313113 Foxb1 forkhead box B1 gene MP:0004162 abnormal mammillary body morphology IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:15654859 1313113 Foxb1 forkhead box B1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:9118797 1313113 Foxb1 forkhead box B1 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:11170346 1313113 Foxb1 forkhead box B1 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11170346 1313113 Foxb1 forkhead box B1 gene MP:0009505 abnormal mammary gland lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:11170346 1313113 Foxb1 forkhead box B1 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:11170346 1313113 Foxb1 forkhead box B1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:9136764 1313113 Foxb1 forkhead box B1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9118797 1313113 Foxb1 forkhead box B1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9136764 1313113 Foxb1 forkhead box B1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9118797 1313113 Foxb1 forkhead box B1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9409663 1313113 Foxb1 forkhead box B1 gene MP:0013718 galactostasis IAGP N RGD:5509061 20150409 MGI PMID:11170346 1313113 Foxb1 forkhead box B1 gene MP:0013718 galactostasis IAGP N RGD:5509061 20150409 MGI PMID:9118797 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220407 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0009362 abnormal primary ovarian follicle morphology IAGP N RGD:5509061 20220407 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313115 Mcm8 minichromosome maintenance 8 homologous recombination repair factor gene MP:0013539 increased ovary adenoma incidence IAGP N RGD:5509061 20150219 MGI PMID:22771120 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0000562 polydactyly IEA N RGD:5509061 20221215 MGI 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0000914 exencephaly IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0000929 open neural tube IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0001293 anophthalmia IEA N RGD:5509061 20221215 MGI 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20221215 MGI 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20221215 MGI 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0004979 abnormal neuronal precursor cell number IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0008797 facial cleft IEA N RGD:5509061 20221215 MGI 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0013210 abnormal primary cilium physiology IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0013213 abnormal embryonic neuroepithelium primary cilium morphology IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313117 Cdk20 cyclin dependent kinase 20 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20180215 MGI PMID:28817564 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20180308 MGI PMID:27680501 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20180308 MGI PMID:27680501 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18344982 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180308 MGI PMID:27680501 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0001513 limb grasping IAGP N RGD:5509061 20180308 MGI PMID:27680501 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20180308 MGI PMID:27680501 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18344982 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18344982 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20180308 MGI PMID:27680501 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18344982 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18344982 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20180308 MGI PMID:27680501 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20180308 MGI PMID:27680501 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20180308 MGI PMID:27680501 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20180308 MGI PMID:27680501 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18344982 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180308 MGI PMID:27680501 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180308 MGI PMID:27680501 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20180308 MGI PMID:27680501 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20180308 MGI PMID:27680501 1313119 Ppm1l protein phosphatase 1 (formerly 2C)-like gene MP:0013438 dysmyelination IAGP N RGD:5509061 20180308 MGI PMID:27680501 1313121 Pgm3 phosphoglucomutase 3 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0008175 absent follicular B cells IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0009154 pancreatic acinar hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17548465 1313121 Pgm3 phosphoglucomutase 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1313125 Sln sarcolipin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200514 MGI PMID:31833196 1313125 Sln sarcolipin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313125 Sln sarcolipin gene MP:0002083 premature death IAGP N RGD:5509061 20200514 MGI PMID:31833196 1313125 Sln sarcolipin gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313125 Sln sarcolipin gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313125 Sln sarcolipin gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313125 Sln sarcolipin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313125 Sln sarcolipin gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313125 Sln sarcolipin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313125 Sln sarcolipin gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17971438 1313125 Sln sarcolipin gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313125 Sln sarcolipin gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313125 Sln sarcolipin gene MP:0009121 increased white fat cell lipid droplet size IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313125 Sln sarcolipin gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313125 Sln sarcolipin gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313125 Sln sarcolipin gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313125 Sln sarcolipin gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313125 Sln sarcolipin gene MP:0011940 decreased food intake IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313125 Sln sarcolipin gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20180111 MGI PMID:22961106 1313126 Ccdc174 coiled-coil domain containing 174 gene MP:0006205 embryonic lethality between implantation and somite formation IEA N RGD:5509061 20141003 MGI 1313126 Ccdc174 coiled-coil domain containing 174 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313126 Ccdc174 coiled-coil domain containing 174 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313127 Kmt5c lysine methyltransferase 5C gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18676810 1313127 Kmt5c lysine methyltransferase 5C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18676810 1313127 Kmt5c lysine methyltransferase 5C gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:18676810 1313127 Kmt5c lysine methyltransferase 5C gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18676810 1313127 Kmt5c lysine methyltransferase 5C gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18676810 1313127 Kmt5c lysine methyltransferase 5C gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:18676810 1313127 Kmt5c lysine methyltransferase 5C gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18676810 1313127 Kmt5c lysine methyltransferase 5C gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18676810 1313127 Kmt5c lysine methyltransferase 5C gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:18676810 1313127 Kmt5c lysine methyltransferase 5C gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:18676810 1313127 Kmt5c lysine methyltransferase 5C gene MP:0008409 increased cellular sensitivity to hydroxyurea IAGP N RGD:5509061 20141003 MGI PMID:18676810 1313127 Kmt5c lysine methyltransferase 5C gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:18676810 1313127 Kmt5c lysine methyltransferase 5C gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18676810 1313127 Kmt5c lysine methyltransferase 5C gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18676810 1313127 Kmt5c lysine methyltransferase 5C gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:18676810 1313129 Smc2 structural maintenance of chromosomes 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20160204 MGI PMID:25474630 1313129 Smc2 structural maintenance of chromosomes 2 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20160204 MGI PMID:25474630 1313129 Smc2 structural maintenance of chromosomes 2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20160204 MGI PMID:25474630 1313129 Smc2 structural maintenance of chromosomes 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20160204 MGI PMID:25474630 1313129 Smc2 structural maintenance of chromosomes 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20160204 MGI PMID:25474630 1313129 Smc2 structural maintenance of chromosomes 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160204 MGI PMID:25474630 1313129 Smc2 structural maintenance of chromosomes 2 gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20160204 MGI PMID:25474630 1313129 Smc2 structural maintenance of chromosomes 2 gene MP:0012204 abnormal neuronal stem cell physiology IAGP N RGD:5509061 20160204 MGI PMID:25474630 1313131 Phf2 PHD finger protein 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23274892 1313131 Phf2 PHD finger protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23274892 1313131 Phf2 PHD finger protein 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23274892 1313131 Phf2 PHD finger protein 2 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:23274892 1313131 Phf2 PHD finger protein 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23274892 1313131 Phf2 PHD finger protein 2 gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:23274892 1313131 Phf2 PHD finger protein 2 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23274892 1313131 Phf2 PHD finger protein 2 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23274892 1313131 Phf2 PHD finger protein 2 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23274892 1313131 Phf2 PHD finger protein 2 gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23274892 1313131 Phf2 PHD finger protein 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23274892 1313131 Phf2 PHD finger protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23274892 1313131 Phf2 PHD finger protein 2 gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20141003 MGI PMID:23274892 1313133 Frmpd1 FERM and PDZ domain containing 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1313133 Frmpd1 FERM and PDZ domain containing 1 gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20240523 MGI 1313133 Frmpd1 FERM and PDZ domain containing 1 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20240523 MGI 1313133 Frmpd1 FERM and PDZ domain containing 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1313135 Reep1 receptor accessory protein 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20150730 MGI PMID:24051375 1313135 Reep1 receptor accessory protein 1 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:24051375 1313135 Reep1 receptor accessory protein 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:24051375 1313135 Reep1 receptor accessory protein 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:24051375 1313135 Reep1 receptor accessory protein 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:24051375 1313135 Reep1 receptor accessory protein 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0005248 abnormal Harderian gland morphology IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:24051375 1313135 Reep1 receptor accessory protein 1 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0009122 decreased white fat cell lipid droplet size IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0010946 hyperpnea IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0012051 spasticity IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0012051 spasticity IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0020211 slow movement IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313135 Reep1 receptor accessory protein 1 gene MP:0030736 increased glutamic acid level IAGP N RGD:5509061 20181004 MGI PMID:27638887 1313135 Reep1 receptor accessory protein 1 gene MP:0031204 hindlimb paresis IAGP N RGD:5509061 20230504 MGI PMID:35348668 1313139 Slc5a10 solute carrier family 5 (sodium/glucose cotransporter), member 10 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23451068 1313139 Slc5a10 solute carrier family 5 (sodium/glucose cotransporter), member 10 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23451068 1313139 Slc5a10 solute carrier family 5 (sodium/glucose cotransporter), member 10 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23451068 1313139 Slc5a10 solute carrier family 5 (sodium/glucose cotransporter), member 10 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23451068 1313139 Slc5a10 solute carrier family 5 (sodium/glucose cotransporter), member 10 gene MP:0002965 increased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:23451068 1313139 Slc5a10 solute carrier family 5 (sodium/glucose cotransporter), member 10 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23451068 1313139 Slc5a10 solute carrier family 5 (sodium/glucose cotransporter), member 10 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23451068 1313139 Slc5a10 solute carrier family 5 (sodium/glucose cotransporter), member 10 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23451068 1313139 Slc5a10 solute carrier family 5 (sodium/glucose cotransporter), member 10 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23451068 1313139 Slc5a10 solute carrier family 5 (sodium/glucose cotransporter), member 10 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23451068 1313139 Slc5a10 solute carrier family 5 (sodium/glucose cotransporter), member 10 gene MP:0010052 increased grip strength IEA N RGD:5509061 20231207 MGI 1313139 Slc5a10 solute carrier family 5 (sodium/glucose cotransporter), member 10 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:23451068 1313139 Slc5a10 solute carrier family 5 (sodium/glucose cotransporter), member 10 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:23451068 1313141 Havcr2 hepatitis A virus cellular receptor 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1313141 Havcr2 hepatitis A virus cellular receptor 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1313141 Havcr2 hepatitis A virus cellular receptor 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1313141 Havcr2 hepatitis A virus cellular receptor 2 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22875804 1313141 Havcr2 hepatitis A virus cellular receptor 2 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230601 MGI 1313141 Havcr2 hepatitis A virus cellular receptor 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20160128 MGI PMID:24567532 1313141 Havcr2 hepatitis A virus cellular receptor 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22875804 1313141 Havcr2 hepatitis A virus cellular receptor 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22875804 1313141 Havcr2 hepatitis A virus cellular receptor 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20160128 MGI PMID:24567532 1313141 Havcr2 hepatitis A virus cellular receptor 2 gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:22875804 1313141 Havcr2 hepatitis A virus cellular receptor 2 gene MP:0010677 decreased activation-induced cell death of T cells IAGP N RGD:5509061 20141003 MGI PMID:22875804 1313141 Havcr2 hepatitis A virus cellular receptor 2 gene MP:0020947 decreased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:22875804 1313141 Havcr2 hepatitis A virus cellular receptor 2 gene MP:0031045 decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:22875804 1313143 Ythdf3 YTH N6-methyladenosine RNA binding protein 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20201022 MGI 1313143 Ythdf3 YTH N6-methyladenosine RNA binding protein 3 gene MP:0000601 small liver IEA N RGD:5509061 20201022 MGI 1313143 Ythdf3 YTH N6-methyladenosine RNA binding protein 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 1313143 Ythdf3 YTH N6-methyladenosine RNA binding protein 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 1313143 Ythdf3 YTH N6-methyladenosine RNA binding protein 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20201224 MGI PMID:30591559 1313143 Ythdf3 YTH N6-methyladenosine RNA binding protein 3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1313143 Ythdf3 YTH N6-methyladenosine RNA binding protein 3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20210128 MGI PMID:32943573 1313143 Ythdf3 YTH N6-methyladenosine RNA binding protein 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20210128 MGI PMID:32943573 1313143 Ythdf3 YTH N6-methyladenosine RNA binding protein 3 gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20201224 MGI PMID:30591559 1313143 Ythdf3 YTH N6-methyladenosine RNA binding protein 3 gene MP:0031023 decreased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20201224 MGI PMID:30591559 1313147 Psmd13 proteasome (prosome, macropain) 26S subunit, non-ATPase, 13 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313147 Psmd13 proteasome (prosome, macropain) 26S subunit, non-ATPase, 13 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313151 Trim32 tripartite motif-containing 32 gene MP:0000730 increased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:22299041 1313151 Trim32 tripartite motif-containing 32 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:21775502 1313151 Trim32 tripartite motif-containing 32 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:19155210 1313151 Trim32 tripartite motif-containing 32 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:22299041 1313151 Trim32 tripartite motif-containing 32 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:21775502 1313151 Trim32 tripartite motif-containing 32 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22299041 1313151 Trim32 tripartite motif-containing 32 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19155210 1313151 Trim32 tripartite motif-containing 32 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19155210 1313151 Trim32 tripartite motif-containing 32 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:19155210 1313151 Trim32 tripartite motif-containing 32 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19155210 1313151 Trim32 tripartite motif-containing 32 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:22299041 1313151 Trim32 tripartite motif-containing 32 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19155210 1313151 Trim32 tripartite motif-containing 32 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21775502 1313151 Trim32 tripartite motif-containing 32 gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:19155210 1313151 Trim32 tripartite motif-containing 32 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19155210 1313151 Trim32 tripartite motif-containing 32 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22299041 1313151 Trim32 tripartite motif-containing 32 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:19155210 1313151 Trim32 tripartite motif-containing 32 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:19155210 1313151 Trim32 tripartite motif-containing 32 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:19155210 1313151 Trim32 tripartite motif-containing 32 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:21775502 1313151 Trim32 tripartite motif-containing 32 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:22299041 1313151 Trim32 tripartite motif-containing 32 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:19155210 1313151 Trim32 tripartite motif-containing 32 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19155210 1313151 Trim32 tripartite motif-containing 32 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:21775502 1313151 Trim32 tripartite motif-containing 32 gene MP:0031328 delayed skeletal muscle regeneration IAGP N RGD:5509061 20220106 MGI PMID:22299041 1313156 Zkscan7 zinc finger with KRAB and SCAN domains 7 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1313156 Zkscan7 zinc finger with KRAB and SCAN domains 7 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1313156 Zkscan7 zinc finger with KRAB and SCAN domains 7 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1313156 Zkscan7 zinc finger with KRAB and SCAN domains 7 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1313156 Zkscan7 zinc finger with KRAB and SCAN domains 7 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1313156 Zkscan7 zinc finger with KRAB and SCAN domains 7 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1313159 Plekha3 pleckstrin homology domain-containing, family A (phosphoinositide binding specific) member 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1313159 Plekha3 pleckstrin homology domain-containing, family A (phosphoinositide binding specific) member 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 1313159 Plekha3 pleckstrin homology domain-containing, family A (phosphoinositide binding specific) member 3 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20181227 MGI 1313163 Abhd17b abhydrolase domain containing 17B gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210128 MGI 1313163 Abhd17b abhydrolase domain containing 17B gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210128 MGI 1313163 Abhd17b abhydrolase domain containing 17B gene MP:0002546 mydriasis IEA N RGD:5509061 20210128 MGI 1313163 Abhd17b abhydrolase domain containing 17B gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1313168 Snrpe small nuclear ribonucleoprotein E gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22258617 1313168 Snrpe small nuclear ribonucleoprotein E gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22258617 1313170 Pdzrn3 PDZ domain containing RING finger 3 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1313170 Pdzrn3 PDZ domain containing RING finger 3 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20160310 MGI PMID:25198863 1313170 Pdzrn3 PDZ domain containing RING finger 3 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20160310 MGI PMID:25198863 1313170 Pdzrn3 PDZ domain containing RING finger 3 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20160310 MGI PMID:25198863 1313170 Pdzrn3 PDZ domain containing RING finger 3 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20160310 MGI PMID:25198863 1313170 Pdzrn3 PDZ domain containing RING finger 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20160310 MGI PMID:25198863 1313170 Pdzrn3 PDZ domain containing RING finger 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160310 MGI PMID:25198863 1313170 Pdzrn3 PDZ domain containing RING finger 3 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20160310 MGI PMID:25198863 1313170 Pdzrn3 PDZ domain containing RING finger 3 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20160310 MGI PMID:25198863 1313170 Pdzrn3 PDZ domain containing RING finger 3 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20160310 MGI PMID:25198863 1313170 Pdzrn3 PDZ domain containing RING finger 3 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20160310 MGI PMID:25198863 1313170 Pdzrn3 PDZ domain containing RING finger 3 gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20160310 MGI PMID:25198863 1313170 Pdzrn3 PDZ domain containing RING finger 3 gene MP:0010664 abnormal vitelline artery morphology IAGP N RGD:5509061 20160310 MGI PMID:25198863 1313170 Pdzrn3 PDZ domain containing RING finger 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1313170 Pdzrn3 PDZ domain containing RING finger 3 gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20160310 MGI PMID:25198863 1313177 Tbc1d30 TBC1 domain family, member 30 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20220811 MGI 1313177 Tbc1d30 TBC1 domain family, member 30 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20181227 MGI 1313177 Tbc1d30 TBC1 domain family, member 30 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1313177 Tbc1d30 TBC1 domain family, member 30 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1313177 Tbc1d30 TBC1 domain family, member 30 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210826 MGI 1313177 Tbc1d30 TBC1 domain family, member 30 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210826 MGI 1313179 Lrrn4 leucine rich repeat neuronal 4 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15870286 1313179 Lrrn4 leucine rich repeat neuronal 4 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15870286 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:2917690 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:8642395 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:18337413 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:18337413 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:8642395 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:23041622 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:18337413 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8642395 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:8642395 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:18337413 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:2917690 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:2917690 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8642395 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18337413 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:2917690 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18337413 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:8642395 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23041622 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:18337413 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:2917690 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:8642395 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:2917690 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0002183 gliosis IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:23041622 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:2917690 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:8642395 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23041622 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18337413 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18337413 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23041622 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:2917690 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0004835 abnormal miniature endplate potential IEA N RGD:5509061 20111116 MGI 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:18337413 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:2917690 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:23041622 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:18337413 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23041622 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23041622 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:18337413 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:2917690 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:18337413 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0009684 abnormal spinal cord lateral motor column morphology IAGP N RGD:5509061 20141003 MGI PMID:8642395 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0010387 abnormal Bergmann glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23041622 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:23041622 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:18337413 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18337413 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20151203 MGI PMID:19625515 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0011730 increased myelin sheath thickness IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20170126 MGI PMID:27911893 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0014331 abnormal Purkinje cell mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:23041622 1313184 Afg3l2 AFG3-like AAA ATPase 2 gene MP:0014345 abnormal neuron mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:19625515 1313186 Cyp4f18 cytochrome P450, family 4, subfamily f, polypeptide 18 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:24632148 1313186 Cyp4f18 cytochrome P450, family 4, subfamily f, polypeptide 18 gene MP:0009817 decreased leukotriene level IAGP N RGD:5509061 20170314 MGI PMID:24632148 1313186 Cyp4f18 cytochrome P450, family 4, subfamily f, polypeptide 18 gene MP:0010953 abnormal fatty acid oxidation IAGP N RGD:5509061 20170314 MGI PMID:24632148 1313188 Golga3 golgin A3 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:23495255 1313188 Golga3 golgin A3 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:23495255 1313188 Golga3 golgin A3 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9892724 1313188 Golga3 golgin A3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23495255 1313188 Golga3 golgin A3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23495255 1313188 Golga3 golgin A3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9892724 1313188 Golga3 golgin A3 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:23495255 1313188 Golga3 golgin A3 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23495255 1313188 Golga3 golgin A3 gene MP:0002686 globozoospermia IEA N RGD:5509061 20141003 MGI 1313188 Golga3 golgin A3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:9892724 1313188 Golga3 golgin A3 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210128 MGI 1313188 Golga3 golgin A3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1313188 Golga3 golgin A3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160421 MGI 1313188 Golga3 golgin A3 gene MP:0004852 decreased testis weight IEA N RGD:5509061 20141003 MGI 1313188 Golga3 golgin A3 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:23495255 1313188 Golga3 golgin A3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:23495255 1313188 Golga3 golgin A3 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20160421 MGI 1313188 Golga3 golgin A3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1313188 Golga3 golgin A3 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23495255 1313188 Golga3 golgin A3 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23495255 1313188 Golga3 golgin A3 gene MP:0008545 absent sperm flagellum IEA N RGD:5509061 20141003 MGI 1313188 Golga3 golgin A3 gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:23495255 1313188 Golga3 golgin A3 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:23495255 1313188 Golga3 golgin A3 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:9892724 1313188 Golga3 golgin A3 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:23495255 1313193 Phf10 PHD finger protein 10 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1313193 Phf10 PHD finger protein 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313195 Arhgap32 Rho GTPase activating protein 32 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20161229 MGI PMID:26979507 1313195 Arhgap32 Rho GTPase activating protein 32 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20161229 MGI PMID:26979507 1313195 Arhgap32 Rho GTPase activating protein 32 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20161229 MGI PMID:26979507 1313195 Arhgap32 Rho GTPase activating protein 32 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20161229 MGI PMID:26979507 1313195 Arhgap32 Rho GTPase activating protein 32 gene MP:0001513 limb grasping IAGP N RGD:5509061 20161229 MGI PMID:26979507 1313195 Arhgap32 Rho GTPase activating protein 32 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20161229 MGI PMID:26979507 1313195 Arhgap32 Rho GTPase activating protein 32 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20161229 MGI PMID:26979507 1313195 Arhgap32 Rho GTPase activating protein 32 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16716191 1313195 Arhgap32 Rho GTPase activating protein 32 gene MP:0011622 abnormal habituation to a novel odor IAGP N RGD:5509061 20161229 MGI PMID:26979507 1313195 Arhgap32 Rho GTPase activating protein 32 gene MP:0012315 impaired learning IAGP N RGD:5509061 20161229 MGI PMID:26979507 1313195 Arhgap32 Rho GTPase activating protein 32 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:26979507 1313195 Arhgap32 Rho GTPase activating protein 32 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161229 MGI PMID:26979507 1313195 Arhgap32 Rho GTPase activating protein 32 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20161229 MGI PMID:26979507 1313195 Arhgap32 Rho GTPase activating protein 32 gene MP:0021117 abnormal huddling behavior IAGP N RGD:5509061 20220519 MGI PMID:26979507 1313197 Amotl1 angiomotin-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190516 MGI PMID:30375152 1313197 Amotl1 angiomotin-like 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20210729 MGI PMID:27464479 1313197 Amotl1 angiomotin-like 1 gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20210729 MGI PMID:27464479 1313197 Amotl1 angiomotin-like 1 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20210729 MGI PMID:27464479 1313197 Amotl1 angiomotin-like 1 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20210729 MGI PMID:27464479 1313197 Amotl1 angiomotin-like 1 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20210729 MGI PMID:27464479 1313197 Amotl1 angiomotin-like 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20190516 MGI PMID:30375152 1313197 Amotl1 angiomotin-like 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20190516 MGI PMID:30375152 1313197 Amotl1 angiomotin-like 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20190516 MGI PMID:30375152 1313198 Limch1 LIM and calponin homology domains 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20240307 MGI PMID:36977593 1313198 Limch1 LIM and calponin homology domains 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1313198 Limch1 LIM and calponin homology domains 1 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20240307 MGI PMID:36977593 1313198 Limch1 LIM and calponin homology domains 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20240307 MGI PMID:36977593 1313198 Limch1 LIM and calponin homology domains 1 gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20240307 MGI PMID:36977593 1313198 Limch1 LIM and calponin homology domains 1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20240307 MGI PMID:36977593 1313198 Limch1 LIM and calponin homology domains 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20240307 MGI PMID:36977593 1313198 Limch1 LIM and calponin homology domains 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1313198 Limch1 LIM and calponin homology domains 1 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20211021 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0000160 kyphosis IAGP N RGD:5509061 20240808 MGI PMID:20429939 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20240523 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240808 MGI PMID:20429939 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0001265 decreased body size IAGP N RGD:5509061 20240808 MGI PMID:20429939 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0001314 cornea opacity IEA N RGD:5509061 20240523 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0001399 hyperactivity IEA N RGD:5509061 20230119 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0001926 female infertility IEA N RGD:5509061 20230119 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20240808 MGI PMID:20429939 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0002083 premature death IAGP N RGD:5509061 20240808 MGI PMID:20429939 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0002574 increased vertical activity IEA N RGD:5509061 20240523 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0002834 decreased heart weight IEA N RGD:5509061 20240523 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20240523 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20240523 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0004024 aneuploidy IAGP N RGD:5509061 20240808 MGI PMID:20429939 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20240808 MGI PMID:20429939 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230119 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0005333 decreased heart rate IEA N RGD:5509061 20240523 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20240523 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20240523 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20240523 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20240523 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20240523 MGI 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20240808 MGI PMID:20429939 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20240808 MGI PMID:20429939 1313200 Topors topoisomerase I binding, arginine/serine-rich gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20240808 MGI PMID:20429939 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20240118 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16317048 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0010496 abnormal pectinate muscle morphology IAGP N RGD:5509061 20240118 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0020135 abnormal heart ventricle wall thickness IAGP N RGD:5509061 20240118 MGI PMID:19652092 1313205 Lims2 LIM and senescent cell antigen like domains 2 gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:19652092 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:18606138 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:10651906 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:10651906 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000158 absent sternum IAGP N RGD:5509061 20141003 MGI PMID:11713269 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:10651906 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11713269 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:10651906 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:11713269 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11713269 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20210520 MGI 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17572674 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:22343533 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:17572674 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22343533 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20171214 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001349 excessive tearing IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10651906 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10651906 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210520 MGI 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:22216013 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20170622 MGI PMID:25043182 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20170622 MGI PMID:25043182 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10651906 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22216013 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:22343533 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:10651906 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18606138 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20221215 MGI 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20141003 MGI PMID:22216013 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210826 MGI 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11713269 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:22343533 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003854 abnormal forelimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003856 abnormal hindlimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003856 abnormal hindlimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20171214 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:22343533 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:10651906 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:11713269 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20170622 MGI PMID:25043182 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18606138 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004472 broad nasal bone IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004595 abnormal mandibular condyloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004622 sacral vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004652 small caudal vertebrae IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004657 small sacral vertebrae IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004667 vertebral body hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004708 short lumbar vertebrae IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:10651906 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17572674 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0006165 entropion IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0006212 large orbits IAGP N RGD:5509061 20170928 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20141003 MGI PMID:22216013 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0008391 abnormal primordial germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22216013 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:22216013 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0008786 abnormal hindgut morphology IAGP N RGD:5509061 20141003 MGI PMID:22216013 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0009284 abnormal sympathetic neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:22343533 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0009575 abnormal pubic symphysis morphology IAGP N RGD:5509061 20181018 MGI PMID:11713269 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10651906 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20170622 MGI PMID:25043182 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:17572674 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:22216013 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11713269 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:10651906 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:18353862 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10651906 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10700181 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11713269 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22343533 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0011772 genital tubercle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0012062 small tail bud IAGP N RGD:5509061 20141003 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20171214 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0014106 delayed chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:10651906 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0014106 delayed chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0030321 abnormal tegmen tympani morphology IAGP N RGD:5509061 20171109 MGI PMID:14745966 1313208 Ror2 receptor tyrosine kinase-like orphan receptor 2 gene MP:0030935 increased primordial germ cell apoptosis IAGP N RGD:5509061 20190411 MGI PMID:22216013 1313213 Adam33 a disintegrin and metallopeptidase domain 33 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16943435 1313213 Adam33 a disintegrin and metallopeptidase domain 33 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1313213 Adam33 a disintegrin and metallopeptidase domain 33 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20211021 MGI 1313215 Cherp calcium homeostasis endoplasmic reticulum protein gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210826 MGI 1313215 Cherp calcium homeostasis endoplasmic reticulum protein gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20240926 MGI 1313215 Cherp calcium homeostasis endoplasmic reticulum protein gene MP:0002718 abnormal inner cell mass morphology IEA N RGD:5509061 20240926 MGI 1313215 Cherp calcium homeostasis endoplasmic reticulum protein gene MP:0005028 abnormal trophectoderm morphology IEA N RGD:5509061 20240926 MGI 1313215 Cherp calcium homeostasis endoplasmic reticulum protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1313215 Cherp calcium homeostasis endoplasmic reticulum protein gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20240926 MGI 1313215 Cherp calcium homeostasis endoplasmic reticulum protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1313215 Cherp calcium homeostasis endoplasmic reticulum protein gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240926 MGI 1313217 Dazap1 DAZ associated protein 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1313217 Dazap1 DAZ associated protein 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1313217 Dazap1 DAZ associated protein 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1313217 Dazap1 DAZ associated protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20230601 MGI 1313217 Dazap1 DAZ associated protein 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20230601 MGI 1313217 Dazap1 DAZ associated protein 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230601 MGI 1313217 Dazap1 DAZ associated protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1313217 Dazap1 DAZ associated protein 1 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18669443 1313217 Dazap1 DAZ associated protein 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:18669443 1313219 Mfsd14a major facilitator superfamily domain containing 14A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160505 MGI PMID:27107036 1313219 Mfsd14a major facilitator superfamily domain containing 14A gene MP:0001925 male infertility IAGP N RGD:5509061 20160505 MGI PMID:27107036 1313219 Mfsd14a major facilitator superfamily domain containing 14A gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20160505 MGI PMID:27107036 1313219 Mfsd14a major facilitator superfamily domain containing 14A gene MP:0002686 globozoospermia IAGP N RGD:5509061 20160505 MGI PMID:27107036 1313219 Mfsd14a major facilitator superfamily domain containing 14A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20160505 MGI PMID:27107036 1313219 Mfsd14a major facilitator superfamily domain containing 14A gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20160505 MGI PMID:27107036 1313219 Mfsd14a major facilitator superfamily domain containing 14A gene MP:0008839 absent acrosome IAGP N RGD:5509061 20160505 MGI PMID:27107036 1313219 Mfsd14a major facilitator superfamily domain containing 14A gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20160505 MGI PMID:27107036 1313219 Mfsd14a major facilitator superfamily domain containing 14A gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20160505 MGI PMID:27107036 1313224 Postn periostin, osteoblast specific factor gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23505553 1313224 Postn periostin, osteoblast specific factor gene MP:0000119 abnormal tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:16497272 1313224 Postn periostin, osteoblast specific factor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:17569887 1313224 Postn periostin, osteoblast specific factor gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:18208976 1313224 Postn periostin, osteoblast specific factor gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:23505553 1313224 Postn periostin, osteoblast specific factor gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1313224 Postn periostin, osteoblast specific factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17569887 1313224 Postn periostin, osteoblast specific factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1313224 Postn periostin, osteoblast specific factor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:20811150 1313224 Postn periostin, osteoblast specific factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:17569887 1313224 Postn periostin, osteoblast specific factor gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:16497272 1313224 Postn periostin, osteoblast specific factor gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:23505553 1313224 Postn periostin, osteoblast specific factor gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:16497272 1313224 Postn periostin, osteoblast specific factor gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20141003 MGI PMID:16497272 1313224 Postn periostin, osteoblast specific factor gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1313224 Postn periostin, osteoblast specific factor gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20811150 1313224 Postn periostin, osteoblast specific factor gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:17569887 1313224 Postn periostin, osteoblast specific factor gene MP:0003668 abnormal periodontal ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0003668 abnormal periodontal ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:16497272 1313224 Postn periostin, osteoblast specific factor gene MP:0003668 abnormal periodontal ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:23505553 1313224 Postn periostin, osteoblast specific factor gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:18190787 1313224 Postn periostin, osteoblast specific factor gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1313224 Postn periostin, osteoblast specific factor gene MP:0003930 abnormal tooth hard tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0003930 abnormal tooth hard tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16497272 1313224 Postn periostin, osteoblast specific factor gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20141003 MGI PMID:23505553 1313224 Postn periostin, osteoblast specific factor gene MP:0004343 small scapula IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0004674 thin ribs IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:23505553 1313224 Postn periostin, osteoblast specific factor gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:17569887 1313224 Postn periostin, osteoblast specific factor gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0005505 thrombocytosis IEA N RGD:5509061 20211021 MGI 1313224 Postn periostin, osteoblast specific factor gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23505553 1313224 Postn periostin, osteoblast specific factor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20811150 1313224 Postn periostin, osteoblast specific factor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0009070 small oviduct IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18208976 1313224 Postn periostin, osteoblast specific factor gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1313224 Postn periostin, osteoblast specific factor gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230601 MGI 1313224 Postn periostin, osteoblast specific factor gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1313224 Postn periostin, osteoblast specific factor gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:23505553 1313224 Postn periostin, osteoblast specific factor gene MP:0010965 decreased compact bone volume IAGP N RGD:5509061 20141003 MGI PMID:23505553 1313224 Postn periostin, osteoblast specific factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20201231 MGI 1313224 Postn periostin, osteoblast specific factor gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:23505553 1313224 Postn periostin, osteoblast specific factor gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1313224 Postn periostin, osteoblast specific factor gene MP:0030132 periodontium inflammation IAGP N RGD:5509061 20171005 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0030451 abnormal dentin mineralization IAGP N RGD:5509061 20180215 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0030494 abnormal molar root morphology IAGP N RGD:5509061 20180125 MGI PMID:16314533 1313224 Postn periostin, osteoblast specific factor gene MP:0030524 abnormal tooth root resorption IAGP N RGD:5509061 20180118 MGI PMID:16314533 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20200514 MGI 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20200514 MGI 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:15606491 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20201022 MGI 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15606491 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15606491 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15606491 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0002059 abnormal seminal vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15606491 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220519 MGI 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:15606491 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:15606491 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0013319 seminal vesicle atrophy IAGP N RGD:5509061 20141204 MGI PMID:15606491 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20210128 MGI 1313226 Plag1 pleiomorphic adenoma gene 1 gene MP:0031362 decreased prostate gland ventral lobe weight IAGP N RGD:5509061 20220303 MGI PMID:15606491 1313229 Haus4 HAUS augmin-like complex, subunit 4 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20240919 MGI 1313229 Haus4 HAUS augmin-like complex, subunit 4 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241017 MGI 1313229 Haus4 HAUS augmin-like complex, subunit 4 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1313229 Haus4 HAUS augmin-like complex, subunit 4 gene MP:0004964 absent inner cell mass IEA N RGD:5509061 20240919 MGI 1313229 Haus4 HAUS augmin-like complex, subunit 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1313229 Haus4 HAUS augmin-like complex, subunit 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1313229 Haus4 HAUS augmin-like complex, subunit 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1313234 Rasip1 Ras interacting protein 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:21396893 1313234 Rasip1 Ras interacting protein 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:21396893 1313234 Rasip1 Ras interacting protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23886837 1313234 Rasip1 Ras interacting protein 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:21396893 1313234 Rasip1 Ras interacting protein 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21396893 1313234 Rasip1 Ras interacting protein 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23886837 1313234 Rasip1 Ras interacting protein 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:23886837 1313234 Rasip1 Ras interacting protein 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23886837 1313234 Rasip1 Ras interacting protein 1 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:21396893 1313234 Rasip1 Ras interacting protein 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21396893 1313234 Rasip1 Ras interacting protein 1 gene MP:0003542 abnormal vascular endothelial cell development IAGP N RGD:5509061 20141003 MGI PMID:21396893 1313234 Rasip1 Ras interacting protein 1 gene MP:0003543 abnormal vascular endothelial cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21396893 1313234 Rasip1 Ras interacting protein 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:23886837 1313234 Rasip1 Ras interacting protein 1 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:21396893 1313234 Rasip1 Ras interacting protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21396893 1313234 Rasip1 Ras interacting protein 1 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:23886837 1313234 Rasip1 Ras interacting protein 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:21396893 1313234 Rasip1 Ras interacting protein 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:23886837 1313234 Rasip1 Ras interacting protein 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:21396893 1313234 Rasip1 Ras interacting protein 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:23886837 1313234 Rasip1 Ras interacting protein 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23886837 1313234 Rasip1 Ras interacting protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21396893 1313234 Rasip1 Ras interacting protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23886837 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220811 MGI 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:11032820 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:11032820 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:11032820 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11032820 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11032820 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11032820 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1313239 Eif4g2 eukaryotic translation initiation factor 4, gamma 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313246 Arid3a AT-rich interaction domain 3A gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1313246 Arid3a AT-rich interaction domain 3A gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20680960 1313246 Arid3a AT-rich interaction domain 3A gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20220519 MGI 1313246 Arid3a AT-rich interaction domain 3A gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1313246 Arid3a AT-rich interaction domain 3A gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1313246 Arid3a AT-rich interaction domain 3A gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20201231 MGI 1313246 Arid3a AT-rich interaction domain 3A gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1313246 Arid3a AT-rich interaction domain 3A gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1313246 Arid3a AT-rich interaction domain 3A gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 1313246 Arid3a AT-rich interaction domain 3A gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1313246 Arid3a AT-rich interaction domain 3A gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1313246 Arid3a AT-rich interaction domain 3A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20680960 1313246 Arid3a AT-rich interaction domain 3A gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20201231 MGI 1313246 Arid3a AT-rich interaction domain 3A gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313246 Arid3a AT-rich interaction domain 3A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313246 Arid3a AT-rich interaction domain 3A gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20680960 1313246 Arid3a AT-rich interaction domain 3A gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21199920 1313248 Krt32 keratin 32 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20231207 MGI 1313248 Krt32 keratin 32 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1313248 Krt32 keratin 32 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1313248 Krt32 keratin 32 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20230601 MGI 1313248 Krt32 keratin 32 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20230601 MGI 1313250 Abce1 ATP-binding cassette, sub-family E member 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1313250 Abce1 ATP-binding cassette, sub-family E member 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1313250 Abce1 ATP-binding cassette, sub-family E member 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20201231 MGI 1313250 Abce1 ATP-binding cassette, sub-family E member 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 1313250 Abce1 ATP-binding cassette, sub-family E member 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1313250 Abce1 ATP-binding cassette, sub-family E member 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1313250 Abce1 ATP-binding cassette, sub-family E member 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20141003 MGI 1313250 Abce1 ATP-binding cassette, sub-family E member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1313250 Abce1 ATP-binding cassette, sub-family E member 1 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 1313250 Abce1 ATP-binding cassette, sub-family E member 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313251 Cdkn2aip CDKN2A interacting protein gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220811 MGI 1313251 Cdkn2aip CDKN2A interacting protein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1313251 Cdkn2aip CDKN2A interacting protein gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20230601 MGI 1313251 Cdkn2aip CDKN2A interacting protein gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11923871 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11923871 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11923871 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17337443 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17485511 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:17470642 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11923871 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17485511 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:11923871 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17470642 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:11923871 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17470642 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17485511 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22550345 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:17470642 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:17485511 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:17470642 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:11923871 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008592 decreased circulating interleukin-1 level IAGP N RGD:5509061 20141003 MGI PMID:11923871 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:11923871 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:17470642 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:17485511 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:11923871 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17470642 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17485511 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:11923871 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17337443 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17470642 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:11923871 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17470642 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17485511 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11923871 1313253 Irak4 interleukin-1 receptor-associated kinase 4 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20230608 MGI PMID:17337443 1313255 Etnk2 ethanolamine kinase 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:16861741 1313255 Etnk2 ethanolamine kinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18755794 1313255 Etnk2 ethanolamine kinase 2 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:16861741 1313259 Epb42 erythrocyte membrane protein band 4.2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:10359562 1313259 Epb42 erythrocyte membrane protein band 4.2 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:10359562 1313259 Epb42 erythrocyte membrane protein band 4.2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10359562 1313259 Epb42 erythrocyte membrane protein band 4.2 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10359562 1313259 Epb42 erythrocyte membrane protein band 4.2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10359562 1313259 Epb42 erythrocyte membrane protein band 4.2 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:10359562 1313259 Epb42 erythrocyte membrane protein band 4.2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:10359562 1313259 Epb42 erythrocyte membrane protein band 4.2 gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:10359562 1313259 Epb42 erythrocyte membrane protein band 4.2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:10359562 1313259 Epb42 erythrocyte membrane protein band 4.2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10359562 1313259 Epb42 erythrocyte membrane protein band 4.2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:10359562 1313259 Epb42 erythrocyte membrane protein band 4.2 gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:10359562 1313259 Epb42 erythrocyte membrane protein band 4.2 gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:10359562 1313262 Zdhhc1 zinc finger, DHHC domain containing 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20201015 MGI PMID:25299331 1313262 Zdhhc1 zinc finger, DHHC domain containing 1 gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20201015 MGI PMID:25299331 1313262 Zdhhc1 zinc finger, DHHC domain containing 1 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20201015 MGI PMID:25299331 1313262 Zdhhc1 zinc finger, DHHC domain containing 1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20201015 MGI PMID:25299331 1313262 Zdhhc1 zinc finger, DHHC domain containing 1 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20201015 MGI PMID:25299331 1313262 Zdhhc1 zinc finger, DHHC domain containing 1 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20201015 MGI PMID:25299331 1313262 Zdhhc1 zinc finger, DHHC domain containing 1 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20201015 MGI PMID:25299331 1313263 Xpnpep3 X-prolyl aminopeptidase 3, mitochondrial gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1313263 Xpnpep3 X-prolyl aminopeptidase 3, mitochondrial gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1313265 Neto2 neuropilin (NRP) and tolloid (TLL)-like 2 gene MP:0000745 tremors IEA N RGD:5509061 20200514 MGI 1313265 Neto2 neuropilin (NRP) and tolloid (TLL)-like 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1313265 Neto2 neuropilin (NRP) and tolloid (TLL)-like 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21734292 1313265 Neto2 neuropilin (NRP) and tolloid (TLL)-like 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1313265 Neto2 neuropilin (NRP) and tolloid (TLL)-like 2 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210520 MGI 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0001127 small ovary IEA N RGD:5509061 20210520 MGI 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:15199137 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15107851 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:15199137 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:15199137 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:15107851 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:15199137 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210128 MGI 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15107851 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15199137 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:15199137 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15107851 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15107851 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15199137 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15107851 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200514 MGI 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15199137 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:15199137 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20141003 MGI PMID:15199137 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15107851 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15199137 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:15107851 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:15107851 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:15107851 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:15107851 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20200514 MGI 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20210513 MGI PMID:31924127 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:15107851 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:15107851 1313269 Cnot7 CCR4-NOT transcription complex, subunit 7 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1313272 Rnf115 ring finger protein 115 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1313272 Rnf115 ring finger protein 115 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1313272 Rnf115 ring finger protein 115 gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20210429 MGI PMID:33139700 1313272 Rnf115 ring finger protein 115 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1313272 Rnf115 ring finger protein 115 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20240523 MGI 1313272 Rnf115 ring finger protein 115 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20210429 MGI PMID:33139700 1313272 Rnf115 ring finger protein 115 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20210429 MGI PMID:33139700 1313272 Rnf115 ring finger protein 115 gene MP:0009790 decreased susceptibility to viral infection induced morbidity/mortality IAGP N RGD:5509061 20210429 MGI PMID:33139700 1313272 Rnf115 ring finger protein 115 gene MP:0009791 increased susceptibility to viral infection induced morbidity/mortality IAGP N RGD:5509061 20210429 MGI PMID:33139700 1313274 Btd biotinidase gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313274 Btd biotinidase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313274 Btd biotinidase gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313274 Btd biotinidase gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313274 Btd biotinidase gene MP:0000756 forelimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313274 Btd biotinidase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313274 Btd biotinidase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313274 Btd biotinidase gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313274 Btd biotinidase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313274 Btd biotinidase gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313274 Btd biotinidase gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313274 Btd biotinidase gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313274 Btd biotinidase gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313274 Btd biotinidase gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313274 Btd biotinidase gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313274 Btd biotinidase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21051254 1313276 Foxb2 forkhead box B2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1313276 Foxb2 forkhead box B2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1313281 Mars1 methionine-tRNA synthetase 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1313281 Mars1 methionine-tRNA synthetase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1313283 Map4k4 mitogen-activated protein kinase kinase kinase kinase 4 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:11290295 1313283 Map4k4 mitogen-activated protein kinase kinase kinase kinase 4 gene MP:0003445 sirenomelia IAGP N RGD:5509061 20141003 MGI PMID:11290295 1313283 Map4k4 mitogen-activated protein kinase kinase kinase kinase 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11290295 1313283 Map4k4 mitogen-activated protein kinase kinase kinase kinase 4 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:11290295 1313283 Map4k4 mitogen-activated protein kinase kinase kinase kinase 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11290295 1313283 Map4k4 mitogen-activated protein kinase kinase kinase kinase 4 gene MP:0012739 abnormal anterior primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:11290295 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201231 MGI 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0001314 cornea opacity IEA N RGD:5509061 20201231 MGI 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:12904583 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20200514 MGI 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0002544 brachydactyly IEA N RGD:5509061 20200514 MGI 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0002764 short tibia IAGP N RGD:5509061 20220714 MGI PMID:34423857 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20141003 MGI PMID:16890158 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0004391 abnormal respiratory conducting tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200514 MGI 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0010079 increased osteochondroma incidence IAGP N RGD:5509061 20220714 MGI PMID:34423857 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20200514 MGI 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0014277 alobar holoprosencephaly IAGP N RGD:5509061 20230810 MGI PMID:17156747 1313287 Spry4 sprouty RTK signaling antagonist 4 gene MP:0031283 increased enchondroma incidence IAGP N RGD:5509061 20220714 MGI PMID:34423857 1313289 Plxna2 plexin A2 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:18327254 1313289 Plxna2 plexin A2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18327254 1313289 Plxna2 plexin A2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18327254 1313289 Plxna2 plexin A2 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20170525 MGI PMID:26319580 1313289 Plxna2 plexin A2 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17296555 1313289 Plxna2 plexin A2 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20484647 1313289 Plxna2 plexin A2 gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:18327254 1313289 Plxna2 plexin A2 gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24179230 1313289 Plxna2 plexin A2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:24179230 1313289 Plxna2 plexin A2 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24179230 1313289 Plxna2 plexin A2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1313289 Plxna2 plexin A2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:18327254 1313289 Plxna2 plexin A2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:24179230 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210805 MGI 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210805 MGI 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210805 MGI 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0001147 small testis IEA N RGD:5509061 20210805 MGI 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20210805 MGI 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210805 MGI 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210805 MGI 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20221215 MGI 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20210805 MGI 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20210819 MGI PMID:29535165 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20210819 MGI PMID:29535165 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20210819 MGI PMID:29535165 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20210805 MGI 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 1313293 Txndc5 thioredoxin domain containing 5 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20240627 MGI 1313294 D5Ertd579e DNA segment, Chr 5, ERATO Doi 579, expressed gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1313294 D5Ertd579e DNA segment, Chr 5, ERATO Doi 579, expressed gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1313294 D5Ertd579e DNA segment, Chr 5, ERATO Doi 579, expressed gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 1313294 D5Ertd579e DNA segment, Chr 5, ERATO Doi 579, expressed gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1313294 D5Ertd579e DNA segment, Chr 5, ERATO Doi 579, expressed gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:17403930 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:17429434 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:17403930 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:17429434 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:17403930 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:17429434 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:17403930 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:22832496 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:17403930 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:17429434 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:22832496 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:17403930 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:17429434 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:22832496 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:17403930 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:17429434 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:17429434 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17403930 1313296 Alox12b arachidonate 12-lipoxygenase, 12R type gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17429434 1313298 Tpst2 protein-tyrosine sulfotransferase 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:18075202 1313298 Tpst2 protein-tyrosine sulfotransferase 2 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:16469738 1313298 Tpst2 protein-tyrosine sulfotransferase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7964294 1313298 Tpst2 protein-tyrosine sulfotransferase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16469738 1313298 Tpst2 protein-tyrosine sulfotransferase 2 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:7964294 1313298 Tpst2 protein-tyrosine sulfotransferase 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18075202 1313298 Tpst2 protein-tyrosine sulfotransferase 2 gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:17456791 1313298 Tpst2 protein-tyrosine sulfotransferase 2 gene MP:0003968 abnormal growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:7964294 1313298 Tpst2 protein-tyrosine sulfotransferase 2 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:7964294 1313298 Tpst2 protein-tyrosine sulfotransferase 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18075202 1313298 Tpst2 protein-tyrosine sulfotransferase 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:18075202 1313298 Tpst2 protein-tyrosine sulfotransferase 2 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:7964294 1313298 Tpst2 protein-tyrosine sulfotransferase 2 gene MP:0008366 enlarged adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:7964294 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21724834 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16354690 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21674502 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:23770245 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20832751 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21674502 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:22624716 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:20832751 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22624716 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20832751 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:20832751 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:21724834 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:20832751 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:21674502 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21674502 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21285512 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21285512 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16354690 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:20362536 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21674502 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:17936560 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16354690 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17936560 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16354690 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22624716 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22624716 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22624716 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17936560 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20832751 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23770245 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15361844 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7477326 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7477327 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:16354690 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:22624716 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11857802 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11857803 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7477326 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7477327 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:16354690 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:21724834 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:16354690 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21724834 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003010 decreased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003010 decreased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:22624716 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16616333 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:22624716 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21724834 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16354690 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:21724834 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17936560 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:21724834 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16354690 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22624716 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0008136 enlarged Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:20832751 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:21674502 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22624716 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0009591 increased liver adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20141003 MGI PMID:7477326 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0010318 increased salivary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22624716 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0010343 increased lipoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21285512 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11857803 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14729946 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15607981 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16616333 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20671749 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21674502 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11431694 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21285512 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17936560 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7477326 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7477327 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15361844 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16354690 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12509446 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832750 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832751 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17526734 1313300 Mdm2 transformed mouse 3T3 cell double minute 2 gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:23770245 1313305 Ciz1 CDKN1A interacting zinc finger protein 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20160602 MGI PMID:27163549 1313305 Ciz1 CDKN1A interacting zinc finger protein 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20160602 MGI PMID:27163549 1313305 Ciz1 CDKN1A interacting zinc finger protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180412 MGI PMID:23583447 1313305 Ciz1 CDKN1A interacting zinc finger protein 1 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20180412 MGI PMID:23583447 1313305 Ciz1 CDKN1A interacting zinc finger protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160602 MGI PMID:27163549 1313305 Ciz1 CDKN1A interacting zinc finger protein 1 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20160602 MGI PMID:27163549 1313305 Ciz1 CDKN1A interacting zinc finger protein 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160602 MGI PMID:27163549 1313305 Ciz1 CDKN1A interacting zinc finger protein 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160602 MGI PMID:27163549 1313305 Ciz1 CDKN1A interacting zinc finger protein 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160602 MGI PMID:27163549 1313305 Ciz1 CDKN1A interacting zinc finger protein 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20160602 MGI PMID:27163549 1313305 Ciz1 CDKN1A interacting zinc finger protein 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20160602 MGI PMID:27163549 1313305 Ciz1 CDKN1A interacting zinc finger protein 1 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20180412 MGI PMID:23583447 1313305 Ciz1 CDKN1A interacting zinc finger protein 1 gene MP:0008409 increased cellular sensitivity to hydroxyurea IAGP N RGD:5509061 20180412 MGI PMID:23583447 1313305 Ciz1 CDKN1A interacting zinc finger protein 1 gene MP:0012563 increased tumor incidence following infection IAGP N RGD:5509061 20180412 MGI PMID:23583447 1313308 Hic2 hypermethylated in cancer 2 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20160218 MGI PMID:24748541 1313308 Hic2 hypermethylated in cancer 2 gene MP:0001785 edema IAGP N RGD:5509061 20160218 MGI PMID:24748541 1313308 Hic2 hypermethylated in cancer 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160218 MGI PMID:24748541 1313308 Hic2 hypermethylated in cancer 2 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20160218 MGI PMID:24748541 1313308 Hic2 hypermethylated in cancer 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20160218 MGI PMID:24748541 1313308 Hic2 hypermethylated in cancer 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160218 MGI PMID:24748541 1313308 Hic2 hypermethylated in cancer 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20160218 MGI PMID:24748541 1313308 Hic2 hypermethylated in cancer 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20160218 MGI PMID:24748541 1313308 Hic2 hypermethylated in cancer 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20160218 MGI PMID:24748541 1313308 Hic2 hypermethylated in cancer 2 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20160218 MGI PMID:24748541 1313308 Hic2 hypermethylated in cancer 2 gene MP:0010770 preweaning lethality IAGP N RGD:5509061 20160218 MGI PMID:24748541 1313308 Hic2 hypermethylated in cancer 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160218 MGI PMID:24748541 1313308 Hic2 hypermethylated in cancer 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20160218 MGI PMID:24748541 1313308 Hic2 hypermethylated in cancer 2 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20160218 MGI PMID:24748541 1313308 Hic2 hypermethylated in cancer 2 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20160218 MGI PMID:24748541 1313310 Dap3 death associated protein 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17135360 1313310 Dap3 death associated protein 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17135360 1313310 Dap3 death associated protein 3 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:17135360 1313310 Dap3 death associated protein 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1313310 Dap3 death associated protein 3 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17135360 1313310 Dap3 death associated protein 3 gene MP:0004258 abnormal placenta size IAGP N RGD:5509061 20141003 MGI PMID:17135360 1313310 Dap3 death associated protein 3 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:17135360 1313310 Dap3 death associated protein 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17135360 1313310 Dap3 death associated protein 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313310 Dap3 death associated protein 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313310 Dap3 death associated protein 3 gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17135360 1313317 Emilin2 elastin microfibril interfacer 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1313317 Emilin2 elastin microfibril interfacer 2 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20160414 MGI PMID:25658937 1313317 Emilin2 elastin microfibril interfacer 2 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20160414 MGI PMID:25658937 1313317 Emilin2 elastin microfibril interfacer 2 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20160414 MGI PMID:25658937 1313317 Emilin2 elastin microfibril interfacer 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1313318 Iglon5 IgLON family member 5 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1313318 Iglon5 IgLON family member 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1313318 Iglon5 IgLON family member 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1313318 Iglon5 IgLON family member 5 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1313318 Iglon5 IgLON family member 5 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20240404 MGI PMID:38370417 1313318 Iglon5 IgLON family member 5 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20240404 MGI PMID:38370417 1313318 Iglon5 IgLON family member 5 gene MP:0001525 impaired balance IAGP N RGD:5509061 20240404 MGI PMID:38370417 1313318 Iglon5 IgLON family member 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1313318 Iglon5 IgLON family member 5 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1313318 Iglon5 IgLON family member 5 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1313318 Iglon5 IgLON family member 5 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1313318 Iglon5 IgLON family member 5 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20240404 MGI PMID:38370417 1313318 Iglon5 IgLON family member 5 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1313318 Iglon5 IgLON family member 5 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20221215 MGI 1313318 Iglon5 IgLON family member 5 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1313318 Iglon5 IgLON family member 5 gene MP:0009710 anhedonia IAGP N RGD:5509061 20240404 MGI PMID:38370417 1313318 Iglon5 IgLON family member 5 gene MP:0020379 abnormal sucrose solution preference IAGP N RGD:5509061 20240404 MGI PMID:38370417 1313321 Farp1 FERM, ARH/RhoGEF and pleckstrin domain protein 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210128 MGI 1313321 Farp1 FERM, ARH/RhoGEF and pleckstrin domain protein 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 1313321 Farp1 FERM, ARH/RhoGEF and pleckstrin domain protein 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1313321 Farp1 FERM, ARH/RhoGEF and pleckstrin domain protein 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1313323 Cep152 centrosomal protein 152 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20150129 MGI PMID:24706806 1313323 Cep152 centrosomal protein 152 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20150129 MGI PMID:24706806 1313323 Cep152 centrosomal protein 152 gene MP:0013214 decreased embryonic neuroepithelium primary cilium number IAGP N RGD:5509061 20150129 MGI PMID:24706806 1313323 Cep152 centrosomal protein 152 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:24706806 1313327 Lyar Ly1 antibody reactive clone gene MP:0000914 exencephaly IAGP N RGD:5509061 20180809 MGI PMID:22815056 1313327 Lyar Ly1 antibody reactive clone gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20180809 MGI PMID:22815056 1313327 Lyar Ly1 antibody reactive clone gene MP:0002083 premature death IAGP N RGD:5509061 20180809 MGI PMID:22815056 1313327 Lyar Ly1 antibody reactive clone gene MP:0003051 curly tail IAGP N RGD:5509061 20180809 MGI PMID:22815056 1313327 Lyar Ly1 antibody reactive clone gene MP:0003054 spina bifida IAGP N RGD:5509061 20180809 MGI PMID:22815056 1313327 Lyar Ly1 antibody reactive clone gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210520 MGI 1313327 Lyar Ly1 antibody reactive clone gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1313327 Lyar Ly1 antibody reactive clone gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180809 MGI PMID:22815056 1313327 Lyar Ly1 antibody reactive clone gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20180809 MGI PMID:22815056 1313329 Matn2 matrilin 2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1313329 Matn2 matrilin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15296947 1313329 Matn2 matrilin 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1313329 Matn2 matrilin 2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1313329 Matn2 matrilin 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1313329 Matn2 matrilin 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1313329 Matn2 matrilin 2 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20210812 MGI PMID:27573814 1313329 Matn2 matrilin 2 gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20210812 MGI PMID:27573814 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0001304 cataract IEA N RGD:5509061 20190502 MGI 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0001762 polyuria IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0002083 premature death IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0002083 premature death IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0002871 albuminuria IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0003606 kidney failure IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0004969 pale kidney IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0005161 hematuria IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0005161 hematuria IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0006325 impaired hearing IEA N RGD:5509061 20111116 MGI 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0009511 distended stomach IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0009644 uremia IEA N RGD:5509061 20111116 MGI 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0011402 renal cast IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0011402 renal cast IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0011418 leukocyturia IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0011425 abnormal kidney interstitium morphology IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0011483 renal glomerular synechia IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20151126 MGI PMID:24522496 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0011871 podocyte hypertrophy IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20210211 MGI PMID:31892712 1313333 Col4a4 collagen, type IV, alpha 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21196518 1313335 Unc45a unc-45 myosin chaperone A gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1313335 Unc45a unc-45 myosin chaperone A gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210128 MGI 1313335 Unc45a unc-45 myosin chaperone A gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210128 MGI 1313335 Unc45a unc-45 myosin chaperone A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313337 B4galt2 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:19265195 1313337 B4galt2 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:19265195 1313337 B4galt2 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:19265195 1313337 B4galt2 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19265195 1313337 B4galt2 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19265195 1313337 B4galt2 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:19265195 1313337 B4galt2 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:19265195 1313337 B4galt2 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:19265195 1313337 B4galt2 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:19265195 1313340 Acap1 ArfGAP with coiled-coil, ankyrin repeat and PH domains 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1313345 Mapkap1 mitogen-activated protein kinase associated protein 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1313345 Mapkap1 mitogen-activated protein kinase associated protein 1 gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20190502 MGI 1313345 Mapkap1 mitogen-activated protein kinase associated protein 1 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:16962653 1313345 Mapkap1 mitogen-activated protein kinase associated protein 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16962653 1313345 Mapkap1 mitogen-activated protein kinase associated protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313345 Mapkap1 mitogen-activated protein kinase associated protein 1 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20210520 MGI 1313345 Mapkap1 mitogen-activated protein kinase associated protein 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1313345 Mapkap1 mitogen-activated protein kinase associated protein 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1313345 Mapkap1 mitogen-activated protein kinase associated protein 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16962653 1313347 Tes testin LIM domain protein gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16033868 1313347 Tes testin LIM domain protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17937400 1313347 Tes testin LIM domain protein gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16033868 1313347 Tes testin LIM domain protein gene MP:0013575 abnormal forestomach-glandular stomach junction morphology IAGP N RGD:5509061 20150305 MGI PMID:16033868 1313347 Tes testin LIM domain protein gene MP:0013576 small forestomach IAGP N RGD:5509061 20150305 MGI PMID:16033868 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:19889634 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:9637690 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:9637690 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9637690 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:9637690 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:9637690 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19889634 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19889634 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:9637690 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:9637690 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:9637690 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9637690 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:9637690 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16807321 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:9637690 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:9637690 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19889634 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0010714 iris coloboma IAGP N RGD:5509061 20141003 MGI PMID:9637690 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19889634 1313349 Hs2st1 heparan sulfate 2-O-sulfotransferase 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9637690 1313351 Gtpbp3 GTP binding protein 3 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1313351 Gtpbp3 GTP binding protein 3 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1313351 Gtpbp3 GTP binding protein 3 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1313351 Gtpbp3 GTP binding protein 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1313353 Klhl40 kelch-like 40 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20160616 MGI PMID:24960163 1313353 Klhl40 kelch-like 40 gene MP:0000751 myopathy IAGP N RGD:5509061 20160616 MGI PMID:24960163 1313353 Klhl40 kelch-like 40 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20160616 MGI PMID:24960163 1313353 Klhl40 kelch-like 40 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160526 MGI PMID:25940086 1313353 Klhl40 kelch-like 40 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160616 MGI PMID:24960163 1313353 Klhl40 kelch-like 40 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160616 MGI PMID:24960163 1313353 Klhl40 kelch-like 40 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20160616 MGI PMID:24960163 1313353 Klhl40 kelch-like 40 gene MP:0002188 small heart IAGP N RGD:5509061 20160616 MGI PMID:24960163 1313353 Klhl40 kelch-like 40 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20160616 MGI PMID:24960163 1313353 Klhl40 kelch-like 40 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20160526 MGI PMID:25940086 1313353 Klhl40 kelch-like 40 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20160616 MGI PMID:24960163 1313353 Klhl40 kelch-like 40 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20160616 MGI PMID:24960163 1313353 Klhl40 kelch-like 40 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20160616 MGI PMID:24960163 1313353 Klhl40 kelch-like 40 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20160526 MGI PMID:25940086 1313353 Klhl40 kelch-like 40 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20160526 MGI PMID:25940086 1313353 Klhl40 kelch-like 40 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160526 MGI PMID:25940086 1313353 Klhl40 kelch-like 40 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160616 MGI PMID:24960163 1313353 Klhl40 kelch-like 40 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1313353 Klhl40 kelch-like 40 gene MP:0020240 increased skeletal muscle cell apoptosis IAGP N RGD:5509061 20160526 MGI PMID:25940086 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:12204261 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:12204261 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:12204261 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:12204261 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11002344 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000615 abnormal palatine gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000615 abnormal palatine gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11002344 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000616 decreased ductal branching in the palatine gland IAGP N RGD:5509061 20141003 MGI PMID:11002344 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000617 increased salivary gland mucosal cell number IAGP N RGD:5509061 20141003 MGI PMID:11002344 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000618 small salivary gland IAGP N RGD:5509061 20141003 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000619 salivary gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000620 narrow salivary ducts IAGP N RGD:5509061 20141003 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000660 prostate gland lateral lobe hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11002344 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000661 small prostate gland ventral lobe IAGP N RGD:5509061 20141003 MGI PMID:11002344 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000664 small prostate gland anterior lobe IAGP N RGD:5509061 20141003 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000664 small prostate gland anterior lobe IAGP N RGD:5509061 20141003 MGI PMID:11002344 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000665 decreased ductal branching in the coagulating gland IAGP N RGD:5509061 20141003 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000665 decreased ductal branching in the coagulating gland IAGP N RGD:5509061 20141003 MGI PMID:11002344 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000666 decreased prostate gland duct number IAGP N RGD:5509061 20141003 MGI PMID:10215624 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000666 decreased prostate gland duct number IAGP N RGD:5509061 20141003 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000666 decreased prostate gland duct number IAGP N RGD:5509061 20141003 MGI PMID:11002344 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0000671 bulbourethral gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10215624 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:11002344 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11002344 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001163 abnormal prostate gland anterior lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:10215624 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001163 abnormal prostate gland anterior lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:11002344 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001163 abnormal prostate gland anterior lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:19494112 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001163 abnormal prostate gland anterior lobe morphology IAGP N RGD:5509061 20220303 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10215624 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11002344 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10215624 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11002344 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001169 abnormal bulbourethral gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22836754 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:10215624 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:10215624 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:11839815 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:15111307 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22836754 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12204261 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12204261 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:10215624 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0003791 abnormal minor salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:12204261 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:12204261 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0005305 prostate gland anterior lobe hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10215624 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0005305 prostate gland anterior lobe hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:12204261 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:11839815 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:11854455 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:15111307 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:18245377 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:19741607 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22836754 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19741607 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22836754 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0009517 abnormal salivary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0009734 abnormal prostate gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:19494112 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0009736 abnormal prostate gland branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10215624 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0009736 abnormal prostate gland branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19494112 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0009736 abnormal prostate gland branching morphogenesis IAGP N RGD:5509061 20220303 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11854455 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22836754 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12204261 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0011781 abnormal bulbourethral gland physiology IAGP N RGD:5509061 20150326 MGI PMID:10215624 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0013736 abnormal bulbourethral gland development IAGP N RGD:5509061 20150416 MGI PMID:10215624 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0013736 abnormal bulbourethral gland development IAGP N RGD:5509061 20150416 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0013737 small bulbourethral gland IAGP N RGD:5509061 20150416 MGI PMID:10906459 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0031369 prostate gland dorsolateral lobe hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:10215624 1313355 Nkx3-1 NK3 homeobox 1 gene MP:0031369 prostate gland dorsolateral lobe hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:10906459 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20160324 MGI PMID:25141153 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17655922 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17655922 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:11973269 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20180215 MGI PMID:23293295 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180215 MGI PMID:28432216 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17655922 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180215 MGI PMID:23293295 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0000610 cholestasis IAGP N RGD:5509061 20180215 MGI PMID:23293295 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0000610 cholestasis IAGP N RGD:5509061 20180215 MGI PMID:28432216 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17655922 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230706 MGI PMID:27606604 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:11973269 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0001687 thin endoderm IAGP N RGD:5509061 20141003 MGI PMID:11973269 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20221006 MGI PMID:36046192 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17655922 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17655922 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180215 MGI PMID:23293295 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180215 MGI PMID:28432216 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160929 MGI PMID:25596186 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20160324 MGI PMID:25141153 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19548312 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22121118 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0002188 small heart IAGP N RGD:5509061 20230706 MGI PMID:27606604 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20160929 MGI PMID:25596186 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:19619492 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20180215 MGI PMID:23293295 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180215 MGI PMID:23293295 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20180215 MGI PMID:23293295 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20160929 MGI PMID:25596186 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17655922 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0003250 absent gallbladder IAGP N RGD:5509061 20141003 MGI PMID:19619492 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0003251 gallbladder inflammation IAGP N RGD:5509061 20180215 MGI PMID:28432216 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0003279 aneurysm IAGP N RGD:5509061 20160929 MGI PMID:25596186 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17655922 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20180215 MGI PMID:23293295 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20160324 MGI PMID:25141153 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0003655 absent pancreas IAGP N RGD:5509061 20141003 MGI PMID:19619492 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17655922 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0004044 aortic dissection IAGP N RGD:5509061 20160929 MGI PMID:25596186 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11973269 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20221006 MGI PMID:36046192 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20180215 MGI PMID:23293295 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:17655922 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20160324 MGI PMID:25141153 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0005084 abnormal gallbladder morphology IAGP N RGD:5509061 20180215 MGI PMID:23293295 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0005084 abnormal gallbladder morphology IAGP N RGD:5509061 20180215 MGI PMID:28432216 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0005085 abnormal gallbladder physiology IAGP N RGD:5509061 20180215 MGI PMID:28432216 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:11973269 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:17655922 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20160324 MGI PMID:25141153 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20160324 MGI PMID:25141153 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20230706 MGI PMID:27606604 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0005385 cardiovascular system phenotype IAGP N RGD:5509061 20230706 MGI PMID:27606604 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0005414 extrahepatic cholestasis IAGP N RGD:5509061 20180215 MGI PMID:23293295 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20160929 MGI PMID:25596186 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0005675 small gallbladder IAGP N RGD:5509061 20180215 MGI PMID:28432216 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0008786 abnormal hindgut morphology IAGP N RGD:5509061 20141003 MGI PMID:11973269 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0008987 abnormal liver lobule morphology IAGP N RGD:5509061 20180215 MGI PMID:23293295 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20160324 MGI PMID:25141153 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0009489 abnormal blood vessel endothelium morphology IAGP N RGD:5509061 20160929 MGI PMID:25596186 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0009492 abnormal gallbladder epithelium morphology IAGP N RGD:5509061 20180215 MGI PMID:23293295 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0009492 abnormal gallbladder epithelium morphology IAGP N RGD:5509061 20180215 MGI PMID:28432216 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0009493 abnormal cystic duct morphology IAGP N RGD:5509061 20180215 MGI PMID:28432216 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0009495 abnormal common bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:19619492 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0009498 abnormal extrahepatic bile duct morphology IAGP N RGD:5509061 20180215 MGI PMID:23293295 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20160324 MGI PMID:25141153 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0009705 abnormal midgut morphology IAGP N RGD:5509061 20141003 MGI PMID:11973269 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0009870 abnormal abdominal aorta morphology IAGP N RGD:5509061 20160929 MGI PMID:25596186 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20230706 MGI PMID:27606604 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0010468 abnormal thoracic aorta morphology IAGP N RGD:5509061 20160929 MGI PMID:25596186 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17655922 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20180215 MGI PMID:28432216 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20180215 MGI PMID:23293295 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11973269 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17655922 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0012084 truncated foregut IAGP N RGD:5509061 20221006 MGI PMID:36046192 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0012201 decreased endothelial cell proliferation IAGP N RGD:5509061 20160929 MGI PMID:25596186 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20160324 MGI PMID:25141153 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20160324 MGI PMID:25141153 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0014010 abnormal peroxisome morphology IAGP N RGD:5509061 20160324 MGI PMID:25141153 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0020134 abnormal gallbladder size IAGP N RGD:5509061 20180215 MGI PMID:28432216 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0031021 abnormal gallbladder smooth muscle morphology IAGP N RGD:5509061 20200227 MGI PMID:28432216 1313359 Sox17 SRY (sex determining region Y)-box 17 gene MP:0031315 biliary atresia IAGP N RGD:5509061 20211104 MGI PMID:28432216 1313361 Ncbp2 nuclear cap binding protein subunit 2 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20181227 MGI 1313361 Ncbp2 nuclear cap binding protein subunit 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313361 Ncbp2 nuclear cap binding protein subunit 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313363 Eif6 eukaryotic translation initiation factor 6 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18784653 1313363 Eif6 eukaryotic translation initiation factor 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18784653 1313363 Eif6 eukaryotic translation initiation factor 6 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:18784653 1313363 Eif6 eukaryotic translation initiation factor 6 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:18784653 1313363 Eif6 eukaryotic translation initiation factor 6 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18784653 1313363 Eif6 eukaryotic translation initiation factor 6 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18784653 1313363 Eif6 eukaryotic translation initiation factor 6 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18784653 1313363 Eif6 eukaryotic translation initiation factor 6 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18784653 1313363 Eif6 eukaryotic translation initiation factor 6 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18784653 1313369 Best2 bestrophin 2 gene MP:0005257 abnormal intraocular pressure IAGP N RGD:5509061 20141003 MGI PMID:18385076 1313369 Best2 bestrophin 2 gene MP:0005260 ocular hypotension IAGP N RGD:5509061 20141003 MGI PMID:18385076 1313369 Best2 bestrophin 2 gene MP:0005544 cornea deposits IEA N RGD:5509061 20201231 MGI 1313369 Best2 bestrophin 2 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18385076 1313369 Best2 bestrophin 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1313373 Clcn6 chloride channel, voltage-sensitive 6 gene MP:0001297 microphthalmia IEA N RGD:5509061 20231207 MGI 1313373 Clcn6 chloride channel, voltage-sensitive 6 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16950870 1313373 Clcn6 chloride channel, voltage-sensitive 6 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16950870 1313373 Clcn6 chloride channel, voltage-sensitive 6 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 1313373 Clcn6 chloride channel, voltage-sensitive 6 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:16950870 1313373 Clcn6 chloride channel, voltage-sensitive 6 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 1313373 Clcn6 chloride channel, voltage-sensitive 6 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:16950870 1313373 Clcn6 chloride channel, voltage-sensitive 6 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16950870 1313373 Clcn6 chloride channel, voltage-sensitive 6 gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20141003 MGI PMID:16950870 1313373 Clcn6 chloride channel, voltage-sensitive 6 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:16950870 1313373 Clcn6 chloride channel, voltage-sensitive 6 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20240523 MGI 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9819431 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:9819431 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17363591 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9819431 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000397 abnormal guard hair morphology IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12810584 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:12810584 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12810584 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:12810584 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:9819431 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9819431 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16271529 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9819431 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:17608565 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:15231717 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17235288 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17363591 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17608565 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:17363591 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17608565 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12810584 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9819431 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16271529 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9819431 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15231717 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9819431 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:9819431 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9819431 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:9819431 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16271529 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002683 delayed fertility IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002765 short fibula IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16271529 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0003109 short femur IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12810584 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0003315 abnormal perineum morphology IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21875955 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17608565 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17608565 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17608565 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17608565 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12810584 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15353549 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004347 abnormal scapular spine morphology IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004355 short radius IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004359 short ulna IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004385 interparietal bone hypoplasia IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004385 interparietal bone hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004444 small supraoccipital bone IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:12810584 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:15353549 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:15353549 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0005161 hematuria IAGP N RGD:5509061 20160915 MGI PMID:25252918 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:17363591 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17608565 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:16271529 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0005299 abnormal eye posterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:17363591 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:16271529 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15231717 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17608565 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:17608565 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0006310 increased retinoblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17235288 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0006310 increased retinoblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17363591 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9819431 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0008160 increased diameter of humerus IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0008161 increased diameter of radius IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0008163 increased diameter of ulna IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0008218 delayed emergence of vibrissae IAGP N RGD:5509061 20141003 MGI PMID:12702649 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20141003 MGI PMID:17608565 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:17608565 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16271529 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:16271529 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16271529 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16271529 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16271529 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20160915 MGI PMID:25252918 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20211021 MGI 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16271529 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20150212 MGI PMID:24710275 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:9819431 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:20585628 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:8682293 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:8682294 1313375 Rbl1 RB transcriptional corepressor like 1 gene MP:0030079 small incisors IAGP N RGD:5509061 20170928 MGI PMID:12702649 1313377 Relt RELT tumor necrosis factor receptor gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20200402 MGI PMID:30138536 1313377 Relt RELT tumor necrosis factor receptor gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20191128 MGI PMID:30506946 1313377 Relt RELT tumor necrosis factor receptor gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20200402 MGI PMID:30138536 1313377 Relt RELT tumor necrosis factor receptor gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20200402 MGI PMID:30138536 1313377 Relt RELT tumor necrosis factor receptor gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20191128 MGI PMID:30506946 1313379 Ube2c ubiquitin-conjugating enzyme E2C gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20240829 MGI PMID:36548081 1313379 Ube2c ubiquitin-conjugating enzyme E2C gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1313379 Ube2c ubiquitin-conjugating enzyme E2C gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1313379 Ube2c ubiquitin-conjugating enzyme E2C gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20240829 MGI PMID:36548081 1313379 Ube2c ubiquitin-conjugating enzyme E2C gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20240829 MGI PMID:36548081 1313379 Ube2c ubiquitin-conjugating enzyme E2C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313379 Ube2c ubiquitin-conjugating enzyme E2C gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20240829 MGI PMID:36548081 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9307064 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0008626 increased circulating interleukin-5 level IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0014350 disorganized spleen B cell follicle IAGP N RGD:5509061 20240104 MGI PMID:17142749 1313381 Arhgdib Rho, GDP dissociation inhibitor beta gene MP:0014471 enhanced B cell migration IAGP N RGD:5509061 20240613 MGI PMID:17142749 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20160915 MGI PMID:23412344 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16651524 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20160915 MGI PMID:23412344 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:22539351 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:22539351 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:16651524 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16651524 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19224198 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0002175 decreased brain weight IEA N RGD:5509061 20210128 MGI 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16651524 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:16651524 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:19224198 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:16651524 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19224198 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20240801 MGI PMID:19224198 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:22539351 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:16651524 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0012415 decreased sarcoma incidence IAGP N RGD:5509061 20160915 MGI PMID:23412344 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0030974 enhanced gluconeogenesis IAGP N RGD:5509061 20200102 MGI PMID:19224198 1313383 Cpt1c carnitine palmitoyltransferase 1c gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:19224198 1313385 Asb16 ankyrin repeat and SOCS box-containing 16 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200514 MGI 1313385 Asb16 ankyrin repeat and SOCS box-containing 16 gene MP:0000277 abnormal heart shape IEA N RGD:5509061 20200514 MGI 1313385 Asb16 ankyrin repeat and SOCS box-containing 16 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20200514 MGI 1313385 Asb16 ankyrin repeat and SOCS box-containing 16 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20200514 MGI 1313385 Asb16 ankyrin repeat and SOCS box-containing 16 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1313393 Plk4 polo like kinase 4 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21791561 1313393 Plk4 polo like kinase 4 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11301255 1313393 Plk4 polo like kinase 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11301255 1313393 Plk4 polo like kinase 4 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11301255 1313393 Plk4 polo like kinase 4 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:21791561 1313393 Plk4 polo like kinase 4 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11301255 1313393 Plk4 polo like kinase 4 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:11301255 1313393 Plk4 polo like kinase 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21791561 1313393 Plk4 polo like kinase 4 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:21791561 1313393 Plk4 polo like kinase 4 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:11301255 1313393 Plk4 polo like kinase 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21791561 1313393 Plk4 polo like kinase 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11301255 1313397 Cpne6 copine VI gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20190307 MGI PMID:27194588 1313397 Cpne6 copine VI gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20190307 MGI PMID:27194588 1313397 Cpne6 copine VI gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20190307 MGI PMID:27194588 1313397 Cpne6 copine VI gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20190307 MGI PMID:27194588 1313397 Cpne6 copine VI gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20190307 MGI PMID:27194588 1313401 Jmjd6 jumonji domain containing 6 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:15345036 1313401 Jmjd6 jumonji domain containing 6 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15615595 1313401 Jmjd6 jumonji domain containing 6 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:15345036 1313401 Jmjd6 jumonji domain containing 6 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15615595 1313401 Jmjd6 jumonji domain containing 6 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:15345036 1313401 Jmjd6 jumonji domain containing 6 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:15615595 1313401 Jmjd6 jumonji domain containing 6 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15345036 1313401 Jmjd6 jumonji domain containing 6 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:15345036 1313401 Jmjd6 jumonji domain containing 6 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1313401 Jmjd6 jumonji domain containing 6 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1313401 Jmjd6 jumonji domain containing 6 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1313401 Jmjd6 jumonji domain containing 6 gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20211021 MGI 1313401 Jmjd6 jumonji domain containing 6 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:15345036 1313401 Jmjd6 jumonji domain containing 6 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:15615595 1313401 Jmjd6 jumonji domain containing 6 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15615595 1313401 Jmjd6 jumonji domain containing 6 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:15345036 1313401 Jmjd6 jumonji domain containing 6 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20181227 MGI 1313401 Jmjd6 jumonji domain containing 6 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:15345036 1313401 Jmjd6 jumonji domain containing 6 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:15615595 1313401 Jmjd6 jumonji domain containing 6 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15345036 1313401 Jmjd6 jumonji domain containing 6 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15615595 1313401 Jmjd6 jumonji domain containing 6 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210520 MGI 1313401 Jmjd6 jumonji domain containing 6 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15345036 1313401 Jmjd6 jumonji domain containing 6 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20181227 MGI 1313401 Jmjd6 jumonji domain containing 6 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15615595 1313401 Jmjd6 jumonji domain containing 6 gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15615595 1313401 Jmjd6 jumonji domain containing 6 gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20141003 MGI PMID:15345036 1313401 Jmjd6 jumonji domain containing 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15345036 1313401 Jmjd6 jumonji domain containing 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313401 Jmjd6 jumonji domain containing 6 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15345036 1313401 Jmjd6 jumonji domain containing 6 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20141003 MGI PMID:15345036 1313403 Rsu1 Ras suppressor protein 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20220811 MGI 1313403 Rsu1 Ras suppressor protein 1 gene MP:0003717 pallor IEA N RGD:5509061 20220811 MGI 1313403 Rsu1 Ras suppressor protein 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210520 MGI 1313403 Rsu1 Ras suppressor protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313405 Rbsn rabenosyn, RAB effector gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20240919 MGI 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0003087 absent allantois IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0005030 absent amnion IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0009593 absent chorion IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0011208 small proamniotic cavity IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0012724 absent head fold IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313407 Taf13 TATA-box binding protein associated factor 13 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20240606 MGI PMID:38593904 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:11961557 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7479980 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20170223 MGI PMID:26114879 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17066036 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170223 MGI PMID:26114879 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20210211 MGI PMID:9696838 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:11114377 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20220407 MGI PMID:34625556 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20210211 MGI PMID:9696838 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17066036 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17066036 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:17426143 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16455962 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12960379 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20210211 MGI PMID:9696838 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20210211 MGI PMID:9696838 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:17548588 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12960379 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17135325 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:17066036 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:7479980 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20201224 MGI PMID:30591559 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16123129 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20150312 MGI PMID:24530055 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:17066036 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20170223 MGI PMID:26114879 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200423 MGI PMID:16985170 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:12960379 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:21458307 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20210211 MGI PMID:9696838 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20141003 MGI PMID:17066036 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20170223 MGI PMID:26114879 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:17190817 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20170223 MGI PMID:26114879 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20200423 MGI PMID:16985170 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20171026 MGI PMID:22802351 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10209048 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17548588 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:17066036 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0004795 decreased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20210211 MGI PMID:9696838 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20170223 MGI PMID:26114879 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:11961557 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:16148148 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17082622 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:12370359 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17190817 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17548588 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20210211 MGI PMID:9696838 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20220616 MGI PMID:34343497 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:17051153 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:7479980 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20200827 MGI PMID:26867177 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:17548588 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200827 MGI PMID:26867177 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200827 MGI PMID:26867177 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008248 abnormal mononuclear phagocyte morphology IAGP N RGD:5509061 20200827 MGI PMID:26867177 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17066036 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16455962 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16455962 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:16455962 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17066036 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20170223 MGI PMID:26114879 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008559 abnormal interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10209048 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:24014876 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:17389237 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:17389237 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20170223 MGI PMID:26114879 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:10209048 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:17066036 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:24014876 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:17066036 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20200827 MGI PMID:26867177 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20210211 MGI PMID:9696838 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17066036 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:24014876 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0009851 abnormal Sertoli cell phagocytosis IAGP N RGD:5509061 20240404 MGI PMID:31712393 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0010750 increased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17082622 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12370359 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18656388 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0010855 pulmonary hyperemia IAGP N RGD:5509061 20210211 MGI PMID:9696838 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20171026 MGI PMID:22802351 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0013023 decreased Ly6C high monocyte number IAGP N RGD:5509061 20200827 MGI PMID:26867177 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:10209048 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:11390995 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:23449591 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0020928 increased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16123129 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0020931 increased susceptibility to Adenoviridae infection IEA N RGD:5509061 20200430 MGI 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16625202 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200514 MGI PMID:7479980 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0020940 increased susceptibility to Togaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:11390995 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0020940 increased susceptibility to Togaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:7479980 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:10400797 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0020947 decreased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:10400797 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16985170 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200827 MGI PMID:26867177 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0020952 increased susceptibility to Paramyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:17135325 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0020952 increased susceptibility to Paramyxoviridae infection IAGP N RGD:5509061 20210211 MGI PMID:9696838 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:9687534 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0031040 increased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:7479980 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0031042 increased susceptibility to Togaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:7479980 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0031045 decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:10400797 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200827 MGI PMID:26867177 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200827 MGI PMID:16985170 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200827 MGI PMID:26867177 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0031050 increased susceptibility to Paramyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20210211 MGI PMID:9696838 1313409 Ifnar1 interferon (alpha and beta) receptor 1 gene MP:0031110 meningitis IAGP N RGD:5509061 20210211 MGI PMID:9696838 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20230119 MGI 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0002175 decreased brain weight IEA N RGD:5509061 20210128 MGI 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20231207 MGI 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20230119 MGI 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0009127 increased brown fat cell number IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0020868 decreased lipogenesis IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313410 Ccdc92 coiled-coil domain containing 92 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20230202 MGI PMID:36594018 1313414 Commd8 COMM domain containing 8 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20190912 MGI PMID:31088898 1313414 Commd8 COMM domain containing 8 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20190912 MGI PMID:31088898 1313414 Commd8 COMM domain containing 8 gene MP:0008191 abnormal follicular B cell physiology IAGP N RGD:5509061 20190912 MGI PMID:31088898 1313414 Commd8 COMM domain containing 8 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20190912 MGI PMID:31088898 1313414 Commd8 COMM domain containing 8 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20190912 MGI PMID:31088898 1313414 Commd8 COMM domain containing 8 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20190912 MGI PMID:31088898 1313414 Commd8 COMM domain containing 8 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20190912 MGI PMID:31088898 1313414 Commd8 COMM domain containing 8 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20190912 MGI PMID:31088898 1313414 Commd8 COMM domain containing 8 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20190912 MGI PMID:31088898 1313414 Commd8 COMM domain containing 8 gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20190912 MGI PMID:31088898 1313414 Commd8 COMM domain containing 8 gene MP:0013940 abnormal plasmablast number IAGP N RGD:5509061 20190912 MGI PMID:31088898 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:22251704 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:22251704 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:22251704 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15210819 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:22251704 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22251704 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22251704 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15210819 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:22251704 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15210819 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22251704 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22251704 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:15210819 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15210819 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:22251704 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22251704 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22251704 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:22251704 1313417 Lect2 leukocyte cell-derived chemotaxin 2 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:22251704 1313420 Smarcd1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20171116 MGI PMID:26586440 1313420 Smarcd1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20171116 MGI PMID:26586440 1313420 Smarcd1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20171116 MGI PMID:26586440 1313420 Smarcd1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20171116 MGI PMID:26586440 1313420 Smarcd1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20171116 MGI PMID:26586440 1313420 Smarcd1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20171116 MGI PMID:26586440 1313420 Smarcd1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20171116 MGI PMID:26586440 1313420 Smarcd1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20171116 MGI PMID:26586440 1313420 Smarcd1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20171116 MGI PMID:26586440 1313420 Smarcd1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20171116 MGI PMID:26586440 1313420 Smarcd1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20171116 MGI PMID:26586440 1313420 Smarcd1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 gene MP:0012338 decreased bile salt level IAGP N RGD:5509061 20171116 MGI PMID:26586440 1313420 Smarcd1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 gene MP:0014480 increased feces cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:26586440 1313422 Ky kyphoscoliosis peptidase gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:7864091 1313422 Ky kyphoscoliosis peptidase gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:4123573 1313422 Ky kyphoscoliosis peptidase gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:6527158 1313422 Ky kyphoscoliosis peptidase gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1313422 Ky kyphoscoliosis peptidase gene MP:0000745 tremors IEA N RGD:5509061 20220519 MGI 1313422 Ky kyphoscoliosis peptidase gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:1372391 1313422 Ky kyphoscoliosis peptidase gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:1372391 1313422 Ky kyphoscoliosis peptidase gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:11136708 1313422 Ky kyphoscoliosis peptidase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:4123573 1313422 Ky kyphoscoliosis peptidase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7864091 1313422 Ky kyphoscoliosis peptidase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:1372391 1313422 Ky kyphoscoliosis peptidase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1313422 Ky kyphoscoliosis peptidase gene MP:0001523 impaired righting response IEA N RGD:5509061 20220519 MGI 1313422 Ky kyphoscoliosis peptidase gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:4123573 1313422 Ky kyphoscoliosis peptidase gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:6527158 1313422 Ky kyphoscoliosis peptidase gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:7864091 1313422 Ky kyphoscoliosis peptidase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:4123573 1313422 Ky kyphoscoliosis peptidase gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:4123573 1313422 Ky kyphoscoliosis peptidase gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:1372391 1313422 Ky kyphoscoliosis peptidase gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:7864091 1313422 Ky kyphoscoliosis peptidase gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:4123573 1313422 Ky kyphoscoliosis peptidase gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:1372391 1313422 Ky kyphoscoliosis peptidase gene MP:0004243 abnormal motor nerve collateral sprouting IAGP N RGD:5509061 20141003 MGI PMID:1372391 1313422 Ky kyphoscoliosis peptidase gene MP:0004684 intervertebral disk degeneration IAGP N RGD:5509061 20141003 MGI PMID:6527158 1313422 Ky kyphoscoliosis peptidase gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220519 MGI 1313422 Ky kyphoscoliosis peptidase gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1313422 Ky kyphoscoliosis peptidase gene MP:0006392 abnormal nucleus pulposus morphology IAGP N RGD:5509061 20141003 MGI PMID:6527158 1313422 Ky kyphoscoliosis peptidase gene MP:0006393 absent nucleus pulposus IAGP N RGD:5509061 20141003 MGI PMID:6527158 1313422 Ky kyphoscoliosis peptidase gene MP:0009424 decreased extensor digitorum longus weight IAGP N RGD:5509061 20141003 MGI PMID:7864091 1313422 Ky kyphoscoliosis peptidase gene MP:0009426 decreased soleus weight IAGP N RGD:5509061 20141003 MGI PMID:7864091 1313422 Ky kyphoscoliosis peptidase gene MP:0010052 increased grip strength IEA N RGD:5509061 20220519 MGI 1313422 Ky kyphoscoliosis peptidase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1313429 Cdc34 cell division cycle 34 gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20181227 MGI 1313429 Cdc34 cell division cycle 34 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1313429 Cdc34 cell division cycle 34 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1313429 Cdc34 cell division cycle 34 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210520 MGI 1313433 Uchl5 ubiquitin carboxyl-terminal esterase L5 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21048919 1313433 Uchl5 ubiquitin carboxyl-terminal esterase L5 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21048919 1313433 Uchl5 ubiquitin carboxyl-terminal esterase L5 gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21048919 1313433 Uchl5 ubiquitin carboxyl-terminal esterase L5 gene MP:0000828 abnormal fourth ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21048919 1313433 Uchl5 ubiquitin carboxyl-terminal esterase L5 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:21048919 1313433 Uchl5 ubiquitin carboxyl-terminal esterase L5 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:21048919 1313433 Uchl5 ubiquitin carboxyl-terminal esterase L5 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20181227 MGI 1313433 Uchl5 ubiquitin carboxyl-terminal esterase L5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21048919 1313433 Uchl5 ubiquitin carboxyl-terminal esterase L5 gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:21048919 1313433 Uchl5 ubiquitin carboxyl-terminal esterase L5 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21048919 1313433 Uchl5 ubiquitin carboxyl-terminal esterase L5 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21048919 1313433 Uchl5 ubiquitin carboxyl-terminal esterase L5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313440 Rars2 arginyl-tRNA synthetase 2, mitochondrial gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1313440 Rars2 arginyl-tRNA synthetase 2, mitochondrial gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1313442 Trmo tRNA methyltransferase O gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1313442 Trmo tRNA methyltransferase O gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20180920 MGI PMID:26098576 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20180920 MGI PMID:26098576 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0002493 increased IgG level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313444 Rubcn RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1313445 Efcab3 EF-hand calcium binding domain 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1313445 Efcab3 EF-hand calcium binding domain 3 gene MP:0005238 increased brain size IAGP N RGD:5509061 20200220 MGI PMID:30275530 1313445 Efcab3 EF-hand calcium binding domain 3 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20200220 MGI PMID:30275530 1313445 Efcab3 EF-hand calcium binding domain 3 gene MP:0008914 enlarged cerebellum IAGP N RGD:5509061 20200220 MGI PMID:30275530 1313445 Efcab3 EF-hand calcium binding domain 3 gene MP:0020563 increased pontine nuclei size IAGP N RGD:5509061 20200220 MGI PMID:30275530 1313450 Supt3 SPT3, SAGA and STAGA complex component gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1313450 Supt3 SPT3, SAGA and STAGA complex component gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1313450 Supt3 SPT3, SAGA and STAGA complex component gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1313450 Supt3 SPT3, SAGA and STAGA complex component gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1313450 Supt3 SPT3, SAGA and STAGA complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313453 Kdm5a lysine demethylase 5A gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17320163 1313453 Kdm5a lysine demethylase 5A gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1313453 Kdm5a lysine demethylase 5A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21788502 1313453 Kdm5a lysine demethylase 5A gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17320163 1313453 Kdm5a lysine demethylase 5A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17320163 1313453 Kdm5a lysine demethylase 5A gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:17320163 1313453 Kdm5a lysine demethylase 5A gene MP:0003364 increased insulinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21788502 1313453 Kdm5a lysine demethylase 5A gene MP:0003492 abnormal involuntary movement IEA N RGD:5509061 20111116 MGI 1313453 Kdm5a lysine demethylase 5A gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17320163 1313453 Kdm5a lysine demethylase 5A gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17320163 1313453 Kdm5a lysine demethylase 5A gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21788502 1313453 Kdm5a lysine demethylase 5A gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:21788502 1313453 Kdm5a lysine demethylase 5A gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21788502 1313453 Kdm5a lysine demethylase 5A gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21788502 1313453 Kdm5a lysine demethylase 5A gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21788502 1313453 Kdm5a lysine demethylase 5A gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21788502 1313453 Kdm5a lysine demethylase 5A gene MP:0011087 neonatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1313453 Kdm5a lysine demethylase 5A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21788502 1313453 Kdm5a lysine demethylase 5A gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:21788502 1313459 Siglecf sialic acid binding Ig-like lectin F gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17272508 1313459 Siglecf sialic acid binding Ig-like lectin F gene MP:0002443 abnormal eosinophil differentiation IAGP N RGD:5509061 20141003 MGI PMID:17272508 1313459 Siglecf sialic acid binding Ig-like lectin F gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17272508 1313459 Siglecf sialic acid binding Ig-like lectin F gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17272508 1313460 Gramd1c GRAM domain containing 1C gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20240530 MGI PMID:38694206 1313460 Gramd1c GRAM domain containing 1C gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20210826 MGI 1313460 Gramd1c GRAM domain containing 1C gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210128 MGI 1313460 Gramd1c GRAM domain containing 1C gene MP:0001513 limb grasping IEA N RGD:5509061 20181227 MGI 1313460 Gramd1c GRAM domain containing 1C gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20240523 MGI 1313460 Gramd1c GRAM domain containing 1C gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20240530 MGI PMID:38694206 1313460 Gramd1c GRAM domain containing 1C gene MP:0002959 increased urine microalbumin level IEA N RGD:5509061 20211021 MGI 1313460 Gramd1c GRAM domain containing 1C gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 1313460 Gramd1c GRAM domain containing 1C gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1313460 Gramd1c GRAM domain containing 1C gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1313460 Gramd1c GRAM domain containing 1C gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20240530 MGI PMID:38694206 1313460 Gramd1c GRAM domain containing 1C gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20240530 MGI PMID:38694206 1313460 Gramd1c GRAM domain containing 1C gene MP:0012338 decreased bile salt level IAGP N RGD:5509061 20240530 MGI PMID:38694206 1313460 Gramd1c GRAM domain containing 1C gene MP:0013275 abnormal xenobiotic metabolism IAGP N RGD:5509061 20240530 MGI PMID:38694206 1313460 Gramd1c GRAM domain containing 1C gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1313460 Gramd1c GRAM domain containing 1C gene MP:0014161 increased circulating cortisol level IAGP N RGD:5509061 20240530 MGI PMID:38694206 1313467 Tex14 testis expressed gene 14 intercellular bridge forming factor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16549803 1313467 Tex14 testis expressed gene 14 intercellular bridge forming factor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16549803 1313467 Tex14 testis expressed gene 14 intercellular bridge forming factor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16549803 1313467 Tex14 testis expressed gene 14 intercellular bridge forming factor gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:16549803 1313467 Tex14 testis expressed gene 14 intercellular bridge forming factor gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16549803 1313467 Tex14 testis expressed gene 14 intercellular bridge forming factor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16549803 1313467 Tex14 testis expressed gene 14 intercellular bridge forming factor gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16549803 1313467 Tex14 testis expressed gene 14 intercellular bridge forming factor gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:16549803 1313469 Cdh20 cadherin 20 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20240523 MGI 1313469 Cdh20 cadherin 20 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1313471 Ubox5 U box domain containing 5 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20220519 MGI 1313471 Ubox5 U box domain containing 5 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200310 MGI 1313471 Ubox5 U box domain containing 5 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1313474 Gramd1b GRAM domain containing 1B gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20191024 MGI PMID:30220461 1313474 Gramd1b GRAM domain containing 1B gene MP:0000914 exencephaly IEA N RGD:5509061 20210520 MGI 1313474 Gramd1b GRAM domain containing 1B gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1313474 Gramd1b GRAM domain containing 1B gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20210520 MGI 1313474 Gramd1b GRAM domain containing 1B gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20191024 MGI PMID:30220461 1313474 Gramd1b GRAM domain containing 1B gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20191024 MGI PMID:30220461 1313474 Gramd1b GRAM domain containing 1B gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20191024 MGI PMID:30220461 1313474 Gramd1b GRAM domain containing 1B gene MP:0008294 abnormal adrenal gland zona fasciculata morphology IAGP N RGD:5509061 20191024 MGI PMID:30220461 1313474 Gramd1b GRAM domain containing 1B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1313474 Gramd1b GRAM domain containing 1B gene MP:0011495 abnormal head shape IEA N RGD:5509061 20210520 MGI 1313476 Prrg2 proline-rich Gla (G-carboxyglutamic acid) polypeptide 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 1313476 Prrg2 proline-rich Gla (G-carboxyglutamic acid) polypeptide 2 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1313478 Ltf lactotransferrin gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20160915 MGI PMID:25057912 1313478 Ltf lactotransferrin gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20220630 MGI PMID:35383354 1313478 Ltf lactotransferrin gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20220630 MGI PMID:35383354 1313478 Ltf lactotransferrin gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220630 MGI PMID:35383354 1313478 Ltf lactotransferrin gene MP:0001926 female infertility IAGP N RGD:5509061 20220630 MGI PMID:35383354 1313478 Ltf lactotransferrin gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220630 MGI PMID:35383354 1313478 Ltf lactotransferrin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24823394 1313478 Ltf lactotransferrin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25057912 1313478 Ltf lactotransferrin gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220630 MGI PMID:35383354 1313478 Ltf lactotransferrin gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20160915 MGI PMID:25057912 1313478 Ltf lactotransferrin gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12482971 1313478 Ltf lactotransferrin gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20160915 MGI PMID:25057912 1313478 Ltf lactotransferrin gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:12482971 1313478 Ltf lactotransferrin gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:12482971 1313478 Ltf lactotransferrin gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:12482971 1313478 Ltf lactotransferrin gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20220630 MGI PMID:35383354 1313478 Ltf lactotransferrin gene MP:0009649 delayed embryo implantation IAGP N RGD:5509061 20220630 MGI PMID:35383354 1313478 Ltf lactotransferrin gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20220630 MGI PMID:35383354 1313478 Ltf lactotransferrin gene MP:0009662 abnormal uterine receptivity IAGP N RGD:5509061 20220630 MGI PMID:35383354 1313478 Ltf lactotransferrin gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20220630 MGI PMID:35383354 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21452199 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:24297939 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21452199 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:24297939 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0003954 abnormal Reichert's membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0008030 abnormal Cajal-Retzius cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20141003 MGI PMID:21452199 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24297939 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21452199 1313481 Pomt2 protein-O-mannosyltransferase 2 gene MP:0012129 failure of blastocyst formation IAGP N RGD:5509061 20141003 MGI PMID:24297939 1313483 Trim11 tripartite motif-containing 11 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20221027 MGI PMID:36192394 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:18957218 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:18957218 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18957218 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18957218 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0000861 disorganized barrel cortex IAGP N RGD:5509061 20141003 MGI PMID:18957218 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18957218 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:17092954 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:20346763 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:22284184 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17092954 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18957218 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:20346763 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:22284184 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:22284184 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:20346763 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:22284184 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0002735 abnormal chemical nociception IAGP N RGD:5509061 20141003 MGI PMID:20346763 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:24327562 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:18957218 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:22284184 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:20346763 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0004562 abnormal inner hair cell synaptic ribbon morphology IAGP N RGD:5509061 20141003 MGI PMID:24327562 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:20346763 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0006075 abnormal retina cone bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17092954 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:20346763 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:17092954 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:22284184 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:22284184 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:17092954 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:20346763 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0009681 abnormal pyramidal decussation morphology IAGP N RGD:5509061 20141003 MGI PMID:18957218 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0009682 abnormal anterior corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:18957218 1313487 Bhlhe22 basic helix-loop-helix family, member e22 gene MP:0009682 abnormal anterior corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:22284184 1313489 Cct8 chaperonin containing TCP1 subunit 8 gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20240926 MGI 1313489 Cct8 chaperonin containing TCP1 subunit 8 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240926 MGI 1313489 Cct8 chaperonin containing TCP1 subunit 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1313489 Cct8 chaperonin containing TCP1 subunit 8 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230601 MGI 1313489 Cct8 chaperonin containing TCP1 subunit 8 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240926 MGI 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0001314 cornea opacity IEA N RGD:5509061 20201231 MGI 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20190502 MGI 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20190502 MGI 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20190502 MGI 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20190502 MGI 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20190502 MGI 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0012246 abnormal hepatic cord morphology IAGP N RGD:5509061 20141003 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20161201 MGI PMID:20498273 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313492 Psmg1 proteasome (prosome, macropain) assembly chaperone 1 gene MP:0013551 decreased cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20161201 MGI PMID:20498273 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000413 polyphalangy IAGP N RGD:5509061 20200310 MGI PMID:6067640 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000464 increased presacral vertebrae number IEA N RGD:5509061 20111116 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000480 increased rib number IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000480 increased rib number IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000482 long fibula IEA N RGD:5509061 20111116 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:6067640 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20200310 MGI PMID:6067640 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000568 ectopic digits IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000568 ectopic digits IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20231207 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000585 kinked tail IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000585 kinked tail IAGP N RGD:5509061 20200310 MGI PMID:6067640 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000592 short tail IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000601 small liver IEA N RGD:5509061 20230119 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000692 small spleen IEA N RGD:5509061 20230119 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0000774 decreased brain size IEA N RGD:5509061 20230119 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20200310 MGI PMID:23727884 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:15156142 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:15156143 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20200310 MGI PMID:15156143 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:15156143 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:15156143 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001314 cornea opacity IEA N RGD:5509061 20230119 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001406 abnormal gait IEA N RGD:5509061 20231207 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001922 reduced male fertility IEA N RGD:5509061 20111116 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:5088020 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:6067640 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20111116 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20200310 MGI PMID:6067640 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230119 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0002543 brachyphalangia IEA N RGD:5509061 20111116 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:15156143 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20200310 MGI PMID:15156143 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:15156143 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0002764 short tibia IAGP N RGD:5509061 20200310 MGI PMID:6067640 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20200310 MGI PMID:15156143 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20200310 MGI PMID:15156143 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20230119 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0004049 increased acute promyelocytic leukemia incidence IAGP N RGD:5509061 20200310 MGI PMID:11106752 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0004372 bowed fibula IEA N RGD:5509061 20111116 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0004642 fused metatarsal bones IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0004642 fused metatarsal bones IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0004651 increased thoracic vertebrae number IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0004679 xiphoid process foramen IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0004694 absent patella IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230119 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200310 MGI PMID:15156142 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0005109 abnormal talus morphology IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0005109 abnormal talus morphology IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:15156142 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:5088020 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0005353 abnormal patella morphology IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0005430 absent fibula IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0005430 absent fibula IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20200310 MGI PMID:15156143 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20200310 MGI PMID:18703361 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0008159 increased diameter of fibula IAGP N RGD:5509061 20200310 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0008159 increased diameter of fibula IAGP N RGD:5509061 20200310 MGI PMID:20338044 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0008159 increased diameter of fibula IAGP N RGD:5509061 20200310 MGI PMID:6067640 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20230119 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:23727884 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20200310 MGI PMID:23727884 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0008985 hemimelia IEA N RGD:5509061 20111116 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20200310 MGI PMID:23727884 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230119 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20200310 MGI PMID:23727884 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0012284 increased sternebra number IEA N RGD:5509061 20200310 MGI 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:15156143 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:10835630 1313496 Zbtb16 zinc finger and BTB domain containing 16 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17158963 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17158963 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17158963 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19619499 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11809801 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19619499 1313499 Ppm1d protein phosphatase 1D magnesium-dependent, delta isoform gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:11809801 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:16702401 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0000537 abnormal urethra morphology IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0000632 abnormal pineal gland morphology IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0000653 abnormal sex gland morphology IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16702401 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16702401 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19251665 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16702401 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19251665 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16702401 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19251665 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16702401 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0003742 narrow head IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:19251665 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16702401 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:16702401 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:19251665 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0005262 coloboma IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20211021 MGI 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0009688 abnormal spinal cord central canal morphology IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16702401 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16702401 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19251665 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16702401 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16702401 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0012303 umbilical vein stenosis IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16702401 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0012704 abnormal embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0012705 increased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20619750 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0013362 absent pineal gland IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0013842 ductus venosus stenosis IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313501 Trp53bp2 transformation related protein 53 binding protein 2 gene MP:0013849 absent abducens nerve IAGP N RGD:5509061 20180809 MGI PMID:27447114 1313503 Gpt2 glutamic pyruvate transaminase (alanine aminotransferase) 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20170216 MGI PMID:27601654 1313503 Gpt2 glutamic pyruvate transaminase (alanine aminotransferase) 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20170216 MGI PMID:27601654 1313503 Gpt2 glutamic pyruvate transaminase (alanine aminotransferase) 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20170216 MGI PMID:27601654 1313503 Gpt2 glutamic pyruvate transaminase (alanine aminotransferase) 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20170216 MGI PMID:27601654 1313503 Gpt2 glutamic pyruvate transaminase (alanine aminotransferase) 2 gene MP:0002083 premature death IAGP N RGD:5509061 20170216 MGI PMID:27601654 1313503 Gpt2 glutamic pyruvate transaminase (alanine aminotransferase) 2 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20170216 MGI PMID:27601654 1313503 Gpt2 glutamic pyruvate transaminase (alanine aminotransferase) 2 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20170216 MGI PMID:27601654 1313503 Gpt2 glutamic pyruvate transaminase (alanine aminotransferase) 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20170216 MGI PMID:27601654 1313503 Gpt2 glutamic pyruvate transaminase (alanine aminotransferase) 2 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20170216 MGI PMID:27601654 1313503 Gpt2 glutamic pyruvate transaminase (alanine aminotransferase) 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20170216 MGI PMID:27601654 1313503 Gpt2 glutamic pyruvate transaminase (alanine aminotransferase) 2 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20170216 MGI PMID:27601654 1313503 Gpt2 glutamic pyruvate transaminase (alanine aminotransferase) 2 gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20170216 MGI PMID:27601654 1313503 Gpt2 glutamic pyruvate transaminase (alanine aminotransferase) 2 gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20170216 MGI PMID:27601654 1313505 Map4k1 mitogen-activated protein kinase kinase kinase kinase 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17115060 1313505 Map4k1 mitogen-activated protein kinase kinase kinase kinase 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19414772 1313505 Map4k1 mitogen-activated protein kinase kinase kinase kinase 1 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:19414772 1313505 Map4k1 mitogen-activated protein kinase kinase kinase kinase 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17115060 1313505 Map4k1 mitogen-activated protein kinase kinase kinase kinase 1 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:17115060 1313505 Map4k1 mitogen-activated protein kinase kinase kinase kinase 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17115060 1313505 Map4k1 mitogen-activated protein kinase kinase kinase kinase 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19414772 1313505 Map4k1 mitogen-activated protein kinase kinase kinase kinase 1 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:19414772 1313505 Map4k1 mitogen-activated protein kinase kinase kinase kinase 1 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:19414772 1313505 Map4k1 mitogen-activated protein kinase kinase kinase kinase 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:19414772 1313508 Fbxo10 F-box protein 10 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210128 MGI 1313508 Fbxo10 F-box protein 10 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1313508 Fbxo10 F-box protein 10 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210128 MGI 1313508 Fbxo10 F-box protein 10 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20210128 MGI 1313508 Fbxo10 F-box protein 10 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1313508 Fbxo10 F-box protein 10 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1313508 Fbxo10 F-box protein 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210729 MGI PMID:33914737 1313508 Fbxo10 F-box protein 10 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1313508 Fbxo10 F-box protein 10 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20201022 MGI 1313508 Fbxo10 F-box protein 10 gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20210128 MGI 1313508 Fbxo10 F-box protein 10 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1313508 Fbxo10 F-box protein 10 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20181227 MGI 1313508 Fbxo10 F-box protein 10 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20181227 MGI 1313511 Prpf8 pre-mRNA processing factor 8 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:20811066 1313511 Prpf8 pre-mRNA processing factor 8 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 1313511 Prpf8 pre-mRNA processing factor 8 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20231207 MGI 1313511 Prpf8 pre-mRNA processing factor 8 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1313511 Prpf8 pre-mRNA processing factor 8 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20811066 1313511 Prpf8 pre-mRNA processing factor 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1313513 Alg8 ALG8 alpha-1,3-glucosyltransferase gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1313513 Alg8 ALG8 alpha-1,3-glucosyltransferase gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1313513 Alg8 ALG8 alpha-1,3-glucosyltransferase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1313513 Alg8 ALG8 alpha-1,3-glucosyltransferase gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20181227 MGI 1313513 Alg8 ALG8 alpha-1,3-glucosyltransferase gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 1313513 Alg8 ALG8 alpha-1,3-glucosyltransferase gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20181227 MGI 1313513 Alg8 ALG8 alpha-1,3-glucosyltransferase gene MP:0002824 abnormal chorioallantoic fusion IEA N RGD:5509061 20181227 MGI 1313513 Alg8 ALG8 alpha-1,3-glucosyltransferase gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1313513 Alg8 ALG8 alpha-1,3-glucosyltransferase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1313513 Alg8 ALG8 alpha-1,3-glucosyltransferase gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1313513 Alg8 ALG8 alpha-1,3-glucosyltransferase gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1313513 Alg8 ALG8 alpha-1,3-glucosyltransferase gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1313513 Alg8 ALG8 alpha-1,3-glucosyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313513 Alg8 ALG8 alpha-1,3-glucosyltransferase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1313518 Atf6 activating transcription factor 6 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17765679 1313518 Atf6 activating transcription factor 6 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17765679 1313518 Atf6 activating transcription factor 6 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20150212 MGI PMID:24225943 1313518 Atf6 activating transcription factor 6 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20220310 MGI PMID:26029869 1313518 Atf6 activating transcription factor 6 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20220310 MGI PMID:26029869 1313518 Atf6 activating transcription factor 6 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20220310 MGI PMID:26029869 1313518 Atf6 activating transcription factor 6 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17765679 1313518 Atf6 activating transcription factor 6 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20220310 MGI PMID:26029869 1313518 Atf6 activating transcription factor 6 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17765679 1313518 Atf6 activating transcription factor 6 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20150212 MGI PMID:24225943 1313518 Atf6 activating transcription factor 6 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:17765680 1313518 Atf6 activating transcription factor 6 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17765679 1313518 Atf6 activating transcription factor 6 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17765680 1313518 Atf6 activating transcription factor 6 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20220310 MGI PMID:26029869 1313518 Atf6 activating transcription factor 6 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20220310 MGI PMID:26029869 1313518 Atf6 activating transcription factor 6 gene MP:0014121 increased pancreatic islet cell apoptosis IAGP N RGD:5509061 20160324 MGI PMID:24225943 1313518 Atf6 activating transcription factor 6 gene MP:0020352 abnormal endoplasmic reticulum physiology IAGP N RGD:5509061 20161013 MGI PMID:17765679 1313518 Atf6 activating transcription factor 6 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:26029869 1313523 L3mbtl3 L3MBTL3 histone methyl-lysine binding protein gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20181227 MGI 1313523 L3mbtl3 L3MBTL3 histone methyl-lysine binding protein gene MP:0000562 polydactyly IEA N RGD:5509061 20210520 MGI 1313523 L3mbtl3 L3MBTL3 histone methyl-lysine binding protein gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20231207 MGI 1313523 L3mbtl3 L3MBTL3 histone methyl-lysine binding protein gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15889154 1313523 L3mbtl3 L3MBTL3 histone methyl-lysine binding protein gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1313523 L3mbtl3 L3MBTL3 histone methyl-lysine binding protein gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1313523 L3mbtl3 L3MBTL3 histone methyl-lysine binding protein gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1313523 L3mbtl3 L3MBTL3 histone methyl-lysine binding protein gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15889154 1313523 L3mbtl3 L3MBTL3 histone methyl-lysine binding protein gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15889154 1313523 L3mbtl3 L3MBTL3 histone methyl-lysine binding protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1313524 Thoc7 THO complex 7 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20240919 MGI 1313524 Thoc7 THO complex 7 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1313524 Thoc7 THO complex 7 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1313524 Thoc7 THO complex 7 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1313524 Thoc7 THO complex 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1313524 Thoc7 THO complex 7 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313526 Mki67 antigen identified by monoclonal antibody Ki 67 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20240523 MGI 1313526 Mki67 antigen identified by monoclonal antibody Ki 67 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20240523 MGI 1313526 Mki67 antigen identified by monoclonal antibody Ki 67 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20240523 MGI 1313526 Mki67 antigen identified by monoclonal antibody Ki 67 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150924 MGI PMID:25092767 1313526 Mki67 antigen identified by monoclonal antibody Ki 67 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 1313526 Mki67 antigen identified by monoclonal antibody Ki 67 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20240523 MGI 1313526 Mki67 antigen identified by monoclonal antibody Ki 67 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20240523 MGI 1313526 Mki67 antigen identified by monoclonal antibody Ki 67 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20210617 MGI PMID:33658388 1313526 Mki67 antigen identified by monoclonal antibody Ki 67 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20210617 MGI PMID:33658388 1313526 Mki67 antigen identified by monoclonal antibody Ki 67 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20210617 MGI PMID:33658388 1313526 Mki67 antigen identified by monoclonal antibody Ki 67 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20240523 MGI 1313526 Mki67 antigen identified by monoclonal antibody Ki 67 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20240523 MGI 1313526 Mki67 antigen identified by monoclonal antibody Ki 67 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 1313526 Mki67 antigen identified by monoclonal antibody Ki 67 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20240523 MGI 1313528 Elp6 elongator acetyltransferase complex subunit 6 gene MP:0001405 impaired coordination IEA N RGD:5509061 20170525 MGI 1313528 Elp6 elongator acetyltransferase complex subunit 6 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1313528 Elp6 elongator acetyltransferase complex subunit 6 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1313528 Elp6 elongator acetyltransferase complex subunit 6 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220519 MGI 1313528 Elp6 elongator acetyltransferase complex subunit 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1313528 Elp6 elongator acetyltransferase complex subunit 6 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1313533 Sfr1 SWI5 dependent recombination repair 1 gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20200402 MGI 1313533 Sfr1 SWI5 dependent recombination repair 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200402 MGI 1313533 Sfr1 SWI5 dependent recombination repair 1 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20200402 MGI 1313533 Sfr1 SWI5 dependent recombination repair 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1313533 Sfr1 SWI5 dependent recombination repair 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1313533 Sfr1 SWI5 dependent recombination repair 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313535 Lrrn2 leucine rich repeat protein 2, neuronal gene MP:0004924 abnormal behavior IEA N RGD:5509061 20141003 MGI 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:17785530 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:7628019 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17785530 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7628019 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17785530 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17785530 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18264106 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9515784 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9515784 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:7628019 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:7628019 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20150326 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:10753224 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:7628019 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17785530 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:9515784 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0008011 intestine polyps IAGP N RGD:5509061 20211021 MGI PMID:34489406 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18264106 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:17785530 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:17785530 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17785530 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:7628019 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0009797 abnormal mismatch repair IAGP N RGD:5509061 20141003 MGI PMID:18264106 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0009797 abnormal mismatch repair IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0009797 abnormal mismatch repair IAGP N RGD:5509061 20141003 MGI PMID:7628019 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17785530 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20624957 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7628019 1313537 Pms2 PMS1 homolog2, mismatch repair system component gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:17785530 1313539 Dpep3 dipeptidase 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210107 MGI PMID:31212048 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210128 MGI 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11265752 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0009706 absent midgut IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11463846 1313547 Runx1t1 RUNX1 translocation partner 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313549 Rnf2 ring finger protein 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12183370 1313549 Rnf2 ring finger protein 2 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18039844 1313549 Rnf2 ring finger protein 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:18039844 1313549 Rnf2 ring finger protein 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:18039844 1313549 Rnf2 ring finger protein 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18039844 1313549 Rnf2 ring finger protein 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18039844 1313549 Rnf2 ring finger protein 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18039844 1313549 Rnf2 ring finger protein 2 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18039844 1313549 Rnf2 ring finger protein 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18039844 1313549 Rnf2 ring finger protein 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12183370 1313549 Rnf2 ring finger protein 2 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12183370 1313549 Rnf2 ring finger protein 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18039844 1313549 Rnf2 ring finger protein 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:18039844 1313549 Rnf2 ring finger protein 2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18039844 1313549 Rnf2 ring finger protein 2 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:12183370 1313549 Rnf2 ring finger protein 2 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:12183370 1313549 Rnf2 ring finger protein 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19755104 1313549 Rnf2 ring finger protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12589020 1313549 Rnf2 ring finger protein 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18039844 1313550 Gpbp1 GC-rich promoter binding protein 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 1313550 Gpbp1 GC-rich promoter binding protein 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 1313550 Gpbp1 GC-rich promoter binding protein 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 1313550 Gpbp1 GC-rich promoter binding protein 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20210128 MGI 1313550 Gpbp1 GC-rich promoter binding protein 1 gene MP:0010511 shortened PR interval IEA N RGD:5509061 20201022 MGI 1313550 Gpbp1 GC-rich promoter binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313550 Gpbp1 GC-rich promoter binding protein 1 gene MP:0011954 shortened PQ interval IEA N RGD:5509061 20201022 MGI 1313555 Plxnb2 plexin B2 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:21122816 1313555 Plxnb2 plexin B2 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20161222 MGI PMID:26579598 1313555 Plxnb2 plexin B2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20161222 MGI PMID:26579598 1313555 Plxnb2 plexin B2 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:17554007 1313555 Plxnb2 plexin B2 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17554007 1313555 Plxnb2 plexin B2 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:17554007 1313555 Plxnb2 plexin B2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:17554007 1313555 Plxnb2 plexin B2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:17554007 1313555 Plxnb2 plexin B2 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17554007 1313555 Plxnb2 plexin B2 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21122816 1313555 Plxnb2 plexin B2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17554007 1313555 Plxnb2 plexin B2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21559415 1313555 Plxnb2 plexin B2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17554007 1313555 Plxnb2 plexin B2 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1313555 Plxnb2 plexin B2 gene MP:0001756 abnormal urination IEA N RGD:5509061 20160804 MGI 1313555 Plxnb2 plexin B2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20161222 MGI PMID:21035938 1313555 Plxnb2 plexin B2 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21122816 1313555 Plxnb2 plexin B2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21559415 1313555 Plxnb2 plexin B2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17554007 1313555 Plxnb2 plexin B2 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20161222 MGI PMID:26579598 1313555 Plxnb2 plexin B2 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:17554007 1313555 Plxnb2 plexin B2 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20161222 MGI PMID:26579598 1313555 Plxnb2 plexin B2 gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20161222 MGI PMID:26579598 1313555 Plxnb2 plexin B2 gene MP:0002989 small kidney IAGP N RGD:5509061 20161222 MGI PMID:21035938 1313555 Plxnb2 plexin B2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:17554007 1313555 Plxnb2 plexin B2 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20161222 MGI PMID:26579598 1313555 Plxnb2 plexin B2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20161222 MGI PMID:21035938 1313555 Plxnb2 plexin B2 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0004017 duplex kidney IAGP N RGD:5509061 20161222 MGI PMID:21035938 1313555 Plxnb2 plexin B2 gene MP:0004041 increased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20161201 MGI PMID:25892012 1313555 Plxnb2 plexin B2 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:17554007 1313555 Plxnb2 plexin B2 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17554007 1313555 Plxnb2 plexin B2 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20161222 MGI PMID:23175841 1313555 Plxnb2 plexin B2 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20161222 MGI PMID:26579598 1313555 Plxnb2 plexin B2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20161222 MGI PMID:21035938 1313555 Plxnb2 plexin B2 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20161222 MGI PMID:26579598 1313555 Plxnb2 plexin B2 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20161222 MGI PMID:26579598 1313555 Plxnb2 plexin B2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20161222 MGI PMID:26579598 1313555 Plxnb2 plexin B2 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20161222 MGI PMID:26579598 1313555 Plxnb2 plexin B2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20161222 MGI PMID:26579598 1313555 Plxnb2 plexin B2 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20161222 MGI PMID:21035938 1313555 Plxnb2 plexin B2 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20161201 MGI PMID:25892012 1313555 Plxnb2 plexin B2 gene MP:0009941 abnormal olfactory bulb interneuron morphology IAGP N RGD:5509061 20161222 MGI PMID:23175841 1313555 Plxnb2 plexin B2 gene MP:0009942 abnormal olfactory bulb granule cell morphology IAGP N RGD:5509061 20161222 MGI PMID:23175841 1313555 Plxnb2 plexin B2 gene MP:0009943 abnormal olfactory bulb periglomerular cell morphology IAGP N RGD:5509061 20161222 MGI PMID:23175841 1313555 Plxnb2 plexin B2 gene MP:0009946 abnormal olfactory bulb layer morphology IAGP N RGD:5509061 20161222 MGI PMID:23175841 1313555 Plxnb2 plexin B2 gene MP:0009950 abnormal olfactory bulb internal plexiform layer morphology IAGP N RGD:5509061 20161222 MGI PMID:23175841 1313555 Plxnb2 plexin B2 gene MP:0009951 abnormal olfactory bulb mitral cell layer morphology IAGP N RGD:5509061 20161222 MGI PMID:23175841 1313555 Plxnb2 plexin B2 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20141003 MGI PMID:21122816 1313555 Plxnb2 plexin B2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17554007 1313555 Plxnb2 plexin B2 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:17554007 1313555 Plxnb2 plexin B2 gene MP:0011493 double ureter IAGP N RGD:5509061 20161222 MGI PMID:21035938 1313555 Plxnb2 plexin B2 gene MP:0011760 abnormal ureteric bud tip morphology IAGP N RGD:5509061 20161222 MGI PMID:21035938 1313555 Plxnb2 plexin B2 gene MP:0011761 abnormal ureteric bud trunk morphology IAGP N RGD:5509061 20161222 MGI PMID:21035938 1313555 Plxnb2 plexin B2 gene MP:0011803 double kidney pelvis IAGP N RGD:5509061 20161222 MGI PMID:21035938 1313555 Plxnb2 plexin B2 gene MP:0012707 incomplete caudal neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:17409257 1313555 Plxnb2 plexin B2 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20161222 MGI PMID:23175841 1313555 Plxnb2 plexin B2 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20161222 MGI PMID:26579598 1313555 Plxnb2 plexin B2 gene MP:0030956 abnormal neuronal precursor cell migration IAGP N RGD:5509061 20190725 MGI PMID:23175841 1313555 Plxnb2 plexin B2 gene MP:0030956 abnormal neuronal precursor cell migration IAGP N RGD:5509061 20190725 MGI PMID:26579598 1313557 Msc musculin gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:12493912 1313557 Msc musculin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12493912 1313557 Msc musculin gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:12493912 1313557 Msc musculin gene MP:0004234 abnormal masticatory muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12493912 1313557 Msc musculin gene MP:0004236 absent masseter muscle IAGP N RGD:5509061 20141003 MGI PMID:12493912 1313557 Msc musculin gene MP:0004237 abnormal pterygoid muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12493912 1313557 Msc musculin gene MP:0004238 absent pterygoid muscle IAGP N RGD:5509061 20141003 MGI PMID:12493912 1313557 Msc musculin gene MP:0004240 absent temporalis muscle IAGP N RGD:5509061 20141003 MGI PMID:12493912 1313557 Msc musculin gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:12493912 1313557 Msc musculin gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:12493912 1313557 Msc musculin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12493912 1313559 Mis18bp1 MIS18 binding protein 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20160804 MGI 1313561 Cotl1 coactosin like F-actin binding protein 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1313561 Cotl1 coactosin like F-actin binding protein 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20170105 MGI 1313561 Cotl1 coactosin like F-actin binding protein 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160811 MGI 1313561 Cotl1 coactosin like F-actin binding protein 1 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1313565 Fam204a family with sequence similarity 204, member A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1313571 Adck5 aarF domain containing kinase 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1313571 Adck5 aarF domain containing kinase 5 gene MP:0002959 increased urine microalbumin level IEA N RGD:5509061 20240523 MGI 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0000125 absent incisors IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0000373 belly spot IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0000380 small hair follicles IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0000416 sparse hair IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0001199 thin skin IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0001212 skin lesions IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0004380 short frontal bone IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0004790 absent upper incisors IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0004791 absent lower incisors IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0005367 renal/urinary system phenotype IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0005385 cardiovascular system phenotype IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0011940 decreased food intake IEA N RGD:5509061 20210128 MGI 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0012725 small sebaceous gland IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0013370 anhidrosis IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0013458 decreased eccrine gland number IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0030178 abnormal scalp morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0030431 wide metopic suture IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313573 Kctd15 potassium channel tetramerisation domain containing 15 gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1313576 Dnpep aspartyl aminopeptidase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:29122955 1313576 Dnpep aspartyl aminopeptidase gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1313576 Dnpep aspartyl aminopeptidase gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1313582 Ppl periplakin gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1313582 Ppl periplakin gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1313582 Ppl periplakin gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1313582 Ppl periplakin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15226441 1313582 Ppl periplakin gene MP:0002989 small kidney IEA N RGD:5509061 20181227 MGI 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20210513 MGI PMID:29853563 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20210513 MGI PMID:29853563 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20141003 MGI 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20210513 MGI PMID:29853563 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0002816 colitis IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20210513 MGI PMID:29853563 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20210513 MGI PMID:29853563 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0013023 decreased Ly6C high monocyte number IAGP N RGD:5509061 20210513 MGI PMID:29853563 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0013799 abnormal intestinal goblet cell physiology IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0013956 decreased colon length IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0014201 abnormal intestinal epithelium physiology IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0014219 decreased intestinal mucosa thickness IAGP N RGD:5509061 20210513 MGI PMID:33219235 1313584 Fam3d FAM3 metabolism regulating signaling molecule D gene MP:0014413 decreased depression-related behavior IEA N RGD:5509061 20240425 MGI 1313585 Rnf31 ring finger protein 31 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20190502 MGI 1313585 Rnf31 ring finger protein 31 gene MP:0000274 enlarged heart IEA N RGD:5509061 20190502 MGI 1313585 Rnf31 ring finger protein 31 gene MP:0001257 increased body length IEA N RGD:5509061 20230720 MGI 1313585 Rnf31 ring finger protein 31 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221103 MGI 1313585 Rnf31 ring finger protein 31 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:23942237 1313585 Rnf31 ring finger protein 31 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23942237 1313585 Rnf31 ring finger protein 31 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:23942237 1313585 Rnf31 ring finger protein 31 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1313585 Rnf31 ring finger protein 31 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20221103 MGI 1313585 Rnf31 ring finger protein 31 gene MP:0004940 abnormal B-1 B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23942237 1313585 Rnf31 ring finger protein 31 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20221103 MGI 1313585 Rnf31 ring finger protein 31 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:23942237 1313585 Rnf31 ring finger protein 31 gene MP:0008170 decreased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:23942237 1313585 Rnf31 ring finger protein 31 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:23942237 1313585 Rnf31 ring finger protein 31 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:23942237 1313585 Rnf31 ring finger protein 31 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:23942237 1313585 Rnf31 ring finger protein 31 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:23942237 1313585 Rnf31 ring finger protein 31 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23942237 1313585 Rnf31 ring finger protein 31 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1313585 Rnf31 ring finger protein 31 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20221103 MGI 1313590 Cables1 CDK5 and Abl enzyme substrate 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:20967545 1313590 Cables1 CDK5 and Abl enzyme substrate 1 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20967545 1313590 Cables1 CDK5 and Abl enzyme substrate 1 gene MP:0001123 dilated uterus IAGP N RGD:5509061 20141003 MGI PMID:14729625 1313590 Cables1 CDK5 and Abl enzyme substrate 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:20967545 1313590 Cables1 CDK5 and Abl enzyme substrate 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:14729625 1313590 Cables1 CDK5 and Abl enzyme substrate 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:14729625 1313590 Cables1 CDK5 and Abl enzyme substrate 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:20967545 1313590 Cables1 CDK5 and Abl enzyme substrate 1 gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14729625 1313590 Cables1 CDK5 and Abl enzyme substrate 1 gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:14729625 1313590 Cables1 CDK5 and Abl enzyme substrate 1 gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:14729625 1313590 Cables1 CDK5 and Abl enzyme substrate 1 gene MP:0008222 decreased hippocampal commissure size IAGP N RGD:5509061 20141003 MGI PMID:20967545 1313590 Cables1 CDK5 and Abl enzyme substrate 1 gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:20967545 1313590 Cables1 CDK5 and Abl enzyme substrate 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:20967545 1313590 Cables1 CDK5 and Abl enzyme substrate 1 gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:14729625 1313590 Cables1 CDK5 and Abl enzyme substrate 1 gene MP:0009094 abnormal endometrial gland morphology IAGP N RGD:5509061 20141003 MGI PMID:14729625 1313597 Gnpda2 glucosamine-6-phosphate deaminase 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 1313597 Gnpda2 glucosamine-6-phosphate deaminase 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20221215 MGI 1313598 B9d1 B9 protein domain 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:22179047 1313598 B9d1 B9 protein domain 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0001260 increased body weight IEA N RGD:5509061 20141003 MGI 1313598 B9d1 B9 protein domain 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:22179047 1313598 B9d1 B9 protein domain 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20141003 MGI 1313598 B9d1 B9 protein domain 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:22179047 1313598 B9d1 B9 protein domain 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0002138 abnormal hepatobiliary system morphology IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:22179047 1313598 B9d1 B9 protein domain 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22179047 1313598 B9d1 B9 protein domain 1 gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0005316 abnormal response to tactile stimuli IEA N RGD:5509061 20141003 MGI 1313598 B9d1 B9 protein domain 1 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22179047 1313598 B9d1 B9 protein domain 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0011293 dilated nephron IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0011408 renal tubule hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0011998 decreased embryonic cilium length IAGP N RGD:5509061 20141120 MGI PMID:21763481 1313598 B9d1 B9 protein domain 1 gene MP:0013197 decreased embryonic cilium number IAGP N RGD:5509061 20141120 MGI PMID:21763481 1313601 Nt5dc2 5'-nucleotidase domain containing 2 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20240523 MGI 1313601 Nt5dc2 5'-nucleotidase domain containing 2 gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1313601 Nt5dc2 5'-nucleotidase domain containing 2 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1313601 Nt5dc2 5'-nucleotidase domain containing 2 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20240523 MGI 1313601 Nt5dc2 5'-nucleotidase domain containing 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1313601 Nt5dc2 5'-nucleotidase domain containing 2 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20220811 MGI 1313601 Nt5dc2 5'-nucleotidase domain containing 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1313603 Pou5f2 POU domain class 5, transcription factor 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:9207130 1313609 Ccl25 C-C motif chemokine ligand 25 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1313609 Ccl25 C-C motif chemokine ligand 25 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:18439426 1313609 Ccl25 C-C motif chemokine ligand 25 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:17548595 1313609 Ccl25 C-C motif chemokine ligand 25 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:18439426 1313609 Ccl25 C-C motif chemokine ligand 25 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1313609 Ccl25 C-C motif chemokine ligand 25 gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:17548595 1313609 Ccl25 C-C motif chemokine ligand 25 gene MP:0008345 abnormal gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17548595 1313609 Ccl25 C-C motif chemokine ligand 25 gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:17548595 1313609 Ccl25 C-C motif chemokine ligand 25 gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:18439426 1313609 Ccl25 C-C motif chemokine ligand 25 gene MP:0008399 abnormal alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18439426 1313609 Ccl25 C-C motif chemokine ligand 25 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21421850 1313609 Ccl25 C-C motif chemokine ligand 25 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1313609 Ccl25 C-C motif chemokine ligand 25 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210826 MGI 1313611 Hspa12a heat shock protein 12A gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20210408 MGI PMID:30455376 1313611 Hspa12a heat shock protein 12A gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20210408 MGI PMID:30742088 1313611 Hspa12a heat shock protein 12A gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20210408 MGI PMID:29530582 1313611 Hspa12a heat shock protein 12A gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20210408 MGI PMID:30742088 1313611 Hspa12a heat shock protein 12A gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20210408 MGI PMID:29530582 1313611 Hspa12a heat shock protein 12A gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20210408 MGI PMID:32332915 1313611 Hspa12a heat shock protein 12A gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210408 MGI PMID:30455376 1313611 Hspa12a heat shock protein 12A gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20210408 MGI PMID:30742088 1313611 Hspa12a heat shock protein 12A gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:30455376 1313615 Tbce tubulin-specific chaperone E gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:1641039 1313615 Tbce tubulin-specific chaperone E gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:2022963 1313615 Tbce tubulin-specific chaperone E gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:1641039 1313615 Tbce tubulin-specific chaperone E gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:1641039 1313615 Tbce tubulin-specific chaperone E gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:1641039 1313615 Tbce tubulin-specific chaperone E gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1313615 Tbce tubulin-specific chaperone E gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1313615 Tbce tubulin-specific chaperone E gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:1641039 1313615 Tbce tubulin-specific chaperone E gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:2022963 1313615 Tbce tubulin-specific chaperone E gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:1641039 1313615 Tbce tubulin-specific chaperone E gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:2022963 1313615 Tbce tubulin-specific chaperone E gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:2022963 1313615 Tbce tubulin-specific chaperone E gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:2022963 1313615 Tbce tubulin-specific chaperone E gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0000098 abnormal vomer bone morphology IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0000440 domed cranium IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0001575 cyanosis IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0002200 abnormal brain ventricular system morphology IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0004450 presphenoid bone hypoplasia IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20160407 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0006302 abnormal ectomesenchyme morphology IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0008581 disorganized photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:20333246 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0008583 absent photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20141003 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:22139371 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0030137 abnormal upper incisor morphology IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0030197 small nasal septum IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0030420 short basicranium IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0030443 abnormal cranial synchondrosis IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0030445 abnormal sphenooccipital synchondrosis IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0030447 abnormal presphenoid synchondrosis IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0030498 abnormal dental lamina morphology IAGP N RGD:5509061 20230413 MGI PMID:27170093 1313619 Arl6 ADP-ribosylation factor-like 6 gene MP:0030966 decreased brain ependyma motile cilium number IAGP N RGD:5509061 20190725 MGI PMID:22139371 1313621 Hectd2 HECT domain E3 ubiquitin protein ligase 2 gene MP:0000149 abnormal scapula morphology IEA N RGD:5509061 20160421 MGI 1313621 Hectd2 HECT domain E3 ubiquitin protein ligase 2 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20160811 MGI 1313621 Hectd2 HECT domain E3 ubiquitin protein ligase 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1313621 Hectd2 HECT domain E3 ubiquitin protein ligase 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1313624 Cfap91 cilia and flagella associated protein 91 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1313624 Cfap91 cilia and flagella associated protein 91 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1313624 Cfap91 cilia and flagella associated protein 91 gene MP:0001925 male infertility IEA N RGD:5509061 20230601 MGI 1313624 Cfap91 cilia and flagella associated protein 91 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1313624 Cfap91 cilia and flagella associated protein 91 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230601 MGI 1313624 Cfap91 cilia and flagella associated protein 91 gene MP:0005238 increased brain size IEA N RGD:5509061 20230601 MGI 1313629 Fbl fibrillarin gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:14612397 1313629 Fbl fibrillarin gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14612397 1313629 Fbl fibrillarin gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14612397 1313633 Cdk14 cyclin dependent kinase 14 gene MP:0002946 delayed axon extension IAGP N RGD:5509061 20231123 MGI PMID:37907898 1313633 Cdk14 cyclin dependent kinase 14 gene MP:0010093 decreased circulating magnesium level IEA N RGD:5509061 20181227 MGI 1313637 Anapc2 anaphase promoting complex subunit 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14724179 1313637 Anapc2 anaphase promoting complex subunit 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:14724179 1313637 Anapc2 anaphase promoting complex subunit 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:14724179 1313637 Anapc2 anaphase promoting complex subunit 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14724179 1313637 Anapc2 anaphase promoting complex subunit 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20120112 MGI 1313637 Anapc2 anaphase promoting complex subunit 2 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:14724179 1313637 Anapc2 anaphase promoting complex subunit 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:14724179 1313637 Anapc2 anaphase promoting complex subunit 2 gene MP:0003326 liver failure IAGP N RGD:5509061 20141003 MGI PMID:14724179 1313637 Anapc2 anaphase promoting complex subunit 2 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:14724179 1313637 Anapc2 anaphase promoting complex subunit 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:14724179 1313637 Anapc2 anaphase promoting complex subunit 2 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:14724179 1313637 Anapc2 anaphase promoting complex subunit 2 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:14724179 1313637 Anapc2 anaphase promoting complex subunit 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14724179 1313638 Ints2 integrator complex subunit 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23226392 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0001194 dermatitis IAGP N RGD:5509061 20160922 MGI PMID:24652767 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0001577 anemia IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:23226392 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:23226392 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0003717 pallor IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0004573 absent limb buds IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23226392 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23226392 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20160922 MGI PMID:24652767 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20160922 MGI PMID:24652767 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0008180 abnormal marginal zone B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23226392 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:23226392 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:23226392 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0009328 delayed heart looping IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0009922 increased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:23226392 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0011733 fused somites IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313643 Eps15 epidermal growth factor receptor pathway substrate 15 gene MP:0030951 abnormal endocytosis IAGP N RGD:5509061 20210318 MGI PMID:30692166 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313645 Rassf2 Ras association (RalGDS/AF-6) domain family member 2 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:22227519 1313652 Nelfa negative elongation factor complex member A, Whsc2 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20231207 MGI 1313652 Nelfa negative elongation factor complex member A, Whsc2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1313652 Nelfa negative elongation factor complex member A, Whsc2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 1313652 Nelfa negative elongation factor complex member A, Whsc2 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 1313652 Nelfa negative elongation factor complex member A, Whsc2 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20231207 MGI 1313652 Nelfa negative elongation factor complex member A, Whsc2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20220519 MGI 1313652 Nelfa negative elongation factor complex member A, Whsc2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1313652 Nelfa negative elongation factor complex member A, Whsc2 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20231207 MGI 1313652 Nelfa negative elongation factor complex member A, Whsc2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313652 Nelfa negative elongation factor complex member A, Whsc2 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1313656 Ttk Ttk protein kinase gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20240919 MGI 1313656 Ttk Ttk protein kinase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:21558374 1313656 Ttk Ttk protein kinase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21558374 1313656 Ttk Ttk protein kinase gene MP:0002718 abnormal inner cell mass morphology IEA N RGD:5509061 20240919 MGI 1313656 Ttk Ttk protein kinase gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:21558374 1313656 Ttk Ttk protein kinase gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:21558374 1313656 Ttk Ttk protein kinase gene MP:0009769 abnormal meiotic spindle assembly checkpoint IAGP N RGD:5509061 20141003 MGI PMID:21558374 1313656 Ttk Ttk protein kinase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1313656 Ttk Ttk protein kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1313656 Ttk Ttk protein kinase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 1313656 Ttk Ttk protein kinase gene MP:0014444 enhanced polar body extrusion IAGP N RGD:5509061 20240509 MGI PMID:21558374 1313659 Nyap2 neuronal tyrosine-phophorylated phosphoinositide 3-kinase adaptor 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20180118 MGI PMID:21946561 1313659 Nyap2 neuronal tyrosine-phophorylated phosphoinositide 3-kinase adaptor 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20180118 MGI PMID:21946561 1313659 Nyap2 neuronal tyrosine-phophorylated phosphoinositide 3-kinase adaptor 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20180118 MGI PMID:21946561 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20220616 MGI PMID:29127143 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:10716941 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:10716941 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10716941 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10716941 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:10716941 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:10716941 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10716941 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23142661 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10716941 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20220616 MGI PMID:29127143 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20220616 MGI PMID:29127143 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20220616 MGI PMID:29127143 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20220616 MGI PMID:29127143 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20220721 MGI PMID:28319097 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10716941 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10716941 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20220721 MGI PMID:28319097 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IEA N RGD:5509061 20141003 MGI 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20160421 MGI 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20220616 MGI PMID:29127143 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20220616 MGI PMID:29127143 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23142661 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20220616 MGI PMID:29127143 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0004975 absent regulatory T cells IAGP N RGD:5509061 20220616 MGI PMID:29127143 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IEA N RGD:5509061 20141003 MGI 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10716941 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20220616 MGI PMID:29127143 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20220616 MGI PMID:29127143 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20220721 MGI PMID:28319097 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10716941 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23142661 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0013583 salivary gland degeneration IAGP N RGD:5509061 20220616 MGI PMID:29127143 1313661 Satb1 special AT-rich sequence binding protein 1 gene MP:0013893 decreased common lymphocyte progenitor cell number IAGP N RGD:5509061 20220721 MGI PMID:28319097 1313663 Xpot exportin, tRNA (nuclear export receptor for tRNAs) gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1313663 Xpot exportin, tRNA (nuclear export receptor for tRNAs) gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20161201 MGI 1313663 Xpot exportin, tRNA (nuclear export receptor for tRNAs) gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20161201 MGI 1313663 Xpot exportin, tRNA (nuclear export receptor for tRNAs) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1313663 Xpot exportin, tRNA (nuclear export receptor for tRNAs) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17961633 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20141003 MGI PMID:22562243 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22562243 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:22562243 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:17961633 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22562243 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:17961633 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17961633 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0009600 hypergranulosis IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19145458 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17961633 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22562243 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22562243 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17961633 1313668 Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) gene MP:0013192 decreased sebaceous gland number IAGP N RGD:5509061 20141127 MGI PMID:19145458 1313670 Upp1 uridine phosphorylase 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313670 Upp1 uridine phosphorylase 1 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:12077348 1313670 Upp1 uridine phosphorylase 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12077348 1313670 Upp1 uridine phosphorylase 1 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:12077348 1313670 Upp1 uridine phosphorylase 1 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:15772079 1313670 Upp1 uridine phosphorylase 1 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313670 Upp1 uridine phosphorylase 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:12077348 1313670 Upp1 uridine phosphorylase 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:12077348 1313670 Upp1 uridine phosphorylase 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:15772079 1313670 Upp1 uridine phosphorylase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:15772079 1313670 Upp1 uridine phosphorylase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313670 Upp1 uridine phosphorylase 1 gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313670 Upp1 uridine phosphorylase 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313670 Upp1 uridine phosphorylase 1 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313670 Upp1 uridine phosphorylase 1 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313670 Upp1 uridine phosphorylase 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15772079 1313670 Upp1 uridine phosphorylase 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15772079 1313670 Upp1 uridine phosphorylase 1 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15772079 1313670 Upp1 uridine phosphorylase 1 gene MP:0009980 abnormal cerebellum dentate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313670 Upp1 uridine phosphorylase 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313670 Upp1 uridine phosphorylase 1 gene MP:0011477 abnormal urine nucleoside level IAGP N RGD:5509061 20141003 MGI PMID:15772079 1313672 Lrfn3 leucine rich repeat and fibronectin type III domain containing 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210520 MGI 1313672 Lrfn3 leucine rich repeat and fibronectin type III domain containing 3 gene MP:0001147 small testis IEA N RGD:5509061 20210520 MGI 1313672 Lrfn3 leucine rich repeat and fibronectin type III domain containing 3 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20171116 MGI PMID:27480238 1313672 Lrfn3 leucine rich repeat and fibronectin type III domain containing 3 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20171116 MGI PMID:27480238 1313672 Lrfn3 leucine rich repeat and fibronectin type III domain containing 3 gene MP:0014375 increased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:27480238 1313672 Lrfn3 leucine rich repeat and fibronectin type III domain containing 3 gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:27480238 1313672 Lrfn3 leucine rich repeat and fibronectin type III domain containing 3 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20180301 MGI PMID:27480238 1313674 Pax2 paired box 2 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11804780 1313674 Pax2 paired box 2 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1313674 Pax2 paired box 2 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1313674 Pax2 paired box 2 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1313674 Pax2 paired box 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0000044 absent organ of Corti IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:11804780 1313674 Pax2 paired box 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:14603255 1313674 Pax2 paired box 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:17047028 1313674 Pax2 paired box 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:22410172 1313674 Pax2 paired box 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:12435636 1313674 Pax2 paired box 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:14603255 1313674 Pax2 paired box 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:22410172 1313674 Pax2 paired box 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:17881463 1313674 Pax2 paired box 2 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:17881463 1313674 Pax2 paired box 2 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0000899 abnormal corpora quadrigemina morphology IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22410172 1313674 Pax2 paired box 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:12435636 1313674 Pax2 paired box 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11929848 1313674 Pax2 paired box 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12435636 1313674 Pax2 paired box 2 gene MP:0001948 vesicoureteral reflux IAGP N RGD:5509061 20141003 MGI PMID:17881463 1313674 Pax2 paired box 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11929848 1313674 Pax2 paired box 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1313674 Pax2 paired box 2 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:10587573 1313674 Pax2 paired box 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:14603255 1313674 Pax2 paired box 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:17881463 1313674 Pax2 paired box 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0003146 absent cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0003146 absent cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:11804780 1313674 Pax2 paired box 2 gene MP:0003146 absent cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0003146 absent cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0003147 absent cochlea IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0003147 absent cochlea IAGP N RGD:5509061 20141003 MGI PMID:11804780 1313674 Pax2 paired box 2 gene MP:0003147 absent cochlea IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0003147 absent cochlea IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:16916509 1313674 Pax2 paired box 2 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:16916509 1313674 Pax2 paired box 2 gene MP:0003164 decreased posterior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:16916509 1313674 Pax2 paired box 2 gene MP:0003166 decreased superior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:16916509 1313674 Pax2 paired box 2 gene MP:0003169 abnormal scala media morphology IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10587573 1313674 Pax2 paired box 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12435636 1313674 Pax2 paired box 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17047028 1313674 Pax2 paired box 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22410172 1313674 Pax2 paired box 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0003534 blind vagina IAGP N RGD:5509061 20141003 MGI PMID:12435636 1313674 Pax2 paired box 2 gene MP:0003535 absent vagina IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0003535 absent vagina IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:12435636 1313674 Pax2 paired box 2 gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0003558 absent uterus IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0003575 absent oviduct IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0003575 absent oviduct IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0003584 bifid ureter IAGP N RGD:5509061 20141003 MGI PMID:17881463 1313674 Pax2 paired box 2 gene MP:0003586 dilated ureter IAGP N RGD:5509061 20141003 MGI PMID:17881463 1313674 Pax2 paired box 2 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:10587573 1313674 Pax2 paired box 2 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:17047028 1313674 Pax2 paired box 2 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0003626 kidney medulla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10587573 1313674 Pax2 paired box 2 gene MP:0003626 kidney medulla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14603255 1313674 Pax2 paired box 2 gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:17881463 1313674 Pax2 paired box 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:10587573 1313674 Pax2 paired box 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:11804780 1313674 Pax2 paired box 2 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:12435636 1313674 Pax2 paired box 2 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:17047028 1313674 Pax2 paired box 2 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0004017 duplex kidney IAGP N RGD:5509061 20141003 MGI PMID:17881463 1313674 Pax2 paired box 2 gene MP:0004195 abnormal kidney calyx morphology IAGP N RGD:5509061 20141003 MGI PMID:14603255 1313674 Pax2 paired box 2 gene MP:0004195 abnormal kidney calyx morphology IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0004267 abnormal optic tract morphology IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0004315 absent vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0004315 absent vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0004317 small vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:16916509 1313674 Pax2 paired box 2 gene MP:0004330 abnormal vestibular saccular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0004369 absent utricle IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0004425 abnormal otolith organ morphology IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:10587573 1313674 Pax2 paired box 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:12435636 1313674 Pax2 paired box 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:14603255 1313674 Pax2 paired box 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:17047028 1313674 Pax2 paired box 2 gene MP:0004717 absent cochlear nerve IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0004729 absent efferent ductules of testis IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:14603255 1313674 Pax2 paired box 2 gene MP:0004922 abnormal common crus morphology IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10587573 1313674 Pax2 paired box 2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17047028 1313674 Pax2 paired box 2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17881463 1313674 Pax2 paired box 2 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15012626 1313674 Pax2 paired box 2 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1313674 Pax2 paired box 2 gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:17881463 1313674 Pax2 paired box 2 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1313674 Pax2 paired box 2 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1313674 Pax2 paired box 2 gene MP:0006106 absent tectum IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0006426 Mullerian duct degeneration IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0006426 Mullerian duct degeneration IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0008065 short endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0008065 short endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:16916509 1313674 Pax2 paired box 2 gene MP:0008066 small endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0008259 abnormal optic disk morphology IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0008259 abnormal optic disk morphology IAGP N RGD:5509061 20190411 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0008307 short scala media IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20141003 MGI PMID:15242798 1313674 Pax2 paired box 2 gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1313674 Pax2 paired box 2 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0009074 Wolffian duct degeneration IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0009074 Wolffian duct degeneration IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0009075 rudimentary Wolffian ducts IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0009076 rudimentary Mullerian ducts IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:15012626 1313674 Pax2 paired box 2 gene MP:0009167 increased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:15012626 1313674 Pax2 paired box 2 gene MP:0009215 absent uterine horn IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0009262 absent semicircular canal ampulla IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0009771 absent optic chiasm IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0009846 abnormal neural crest morphology IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0010118 abnormal intermediate mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0010716 optic disk coloboma IAGP N RGD:5509061 20141003 MGI PMID:11929848 1313674 Pax2 paired box 2 gene MP:0010717 optic nerve coloboma IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0010980 ectopic ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:17881463 1313674 Pax2 paired box 2 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:12435636 1313674 Pax2 paired box 2 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0010986 abnormal mesonephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14603255 1313674 Pax2 paired box 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15012626 1313674 Pax2 paired box 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22410172 1313674 Pax2 paired box 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14603255 1313674 Pax2 paired box 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17047028 1313674 Pax2 paired box 2 gene MP:0011238 abnormal inner ear development IAGP N RGD:5509061 20240822 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:10587573 1313674 Pax2 paired box 2 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:12435636 1313674 Pax2 paired box 2 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:14603255 1313674 Pax2 paired box 2 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:22410172 1313674 Pax2 paired box 2 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20141003 MGI PMID:22410172 1313674 Pax2 paired box 2 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:10587573 1313674 Pax2 paired box 2 gene MP:0011360 kidney cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0011365 small metanephros IAGP N RGD:5509061 20141003 MGI PMID:12435636 1313674 Pax2 paired box 2 gene MP:0011366 absent metanephros IAGP N RGD:5509061 20141003 MGI PMID:12435636 1313674 Pax2 paired box 2 gene MP:0011366 absent metanephros IAGP N RGD:5509061 20141003 MGI PMID:8575306 1313674 Pax2 paired box 2 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10587573 1313674 Pax2 paired box 2 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14603255 1313674 Pax2 paired box 2 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16609680 1313674 Pax2 paired box 2 gene MP:0011382 abnormal kidney lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:22410172 1313674 Pax2 paired box 2 gene MP:0011493 double ureter IAGP N RGD:5509061 20141003 MGI PMID:17881463 1313674 Pax2 paired box 2 gene MP:0011493 double ureter IAGP N RGD:5509061 20141003 MGI PMID:22410172 1313674 Pax2 paired box 2 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20141003 MGI PMID:8943028 1313674 Pax2 paired box 2 gene MP:0012533 uveal coloboma IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313674 Pax2 paired box 2 gene MP:0012535 abnormal optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:10934015 1313674 Pax2 paired box 2 gene MP:0012535 abnormal optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:8951055 1313674 Pax2 paired box 2 gene MP:0012536 delayed optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:20221250 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:15608054 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:16484451 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:16511604 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:15608054 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:20805469 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:20805469 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:15608054 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000469 abnormal esophageal squamous epithelium morphology IAGP N RGD:5509061 20160407 MGI PMID:25652409 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20160407 MGI PMID:25652409 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:15608054 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:15608054 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001221 epidermal atrophy IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20421363 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20439468 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20805469 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:20421363 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:15608054 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:16484451 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:16511604 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:16484451 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15608054 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16511604 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15608054 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16511604 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20421363 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20805469 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:15608054 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0002980 abnormal postural reflex IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15608054 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16511604 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:20805469 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0004548 dilated esophagus IAGP N RGD:5509061 20160407 MGI PMID:25652409 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0004675 rib fractures IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0004675 rib fractures IAGP N RGD:5509061 20141003 MGI PMID:20421363 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0004675 rib fractures IAGP N RGD:5509061 20141003 MGI PMID:20439468 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:20805469 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0005114 premature hair loss IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:20805469 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15608054 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:15608054 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:16484451 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:20421363 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:20421363 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20805469 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0009480 distended cecum IAGP N RGD:5509061 20160407 MGI PMID:25652409 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0009878 decreased susceptibility to bone fracture IAGP N RGD:5509061 20141003 MGI PMID:20439468 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0011009 increased circulating glutamate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20439468 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0011195 increased hair follicle apoptosis IAGP N RGD:5509061 20181129 MGI PMID:11923874 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0011570 esophageal achalasia IAGP N RGD:5509061 20160407 MGI PMID:25652409 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0021188 decreased bone mineral density of presacral vertebrae IAGP N RGD:5509061 20220915 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0030082 long lower incisors IAGP N RGD:5509061 20171005 MGI PMID:12235369 1313678 Zmpste24 zinc metallopeptidase, STE24 gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:12235369 1313680 Cnnm4 cyclin M4 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20150618 MGI PMID:24339795 1313680 Cnnm4 cyclin M4 gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20150618 MGI PMID:24339795 1313680 Cnnm4 cyclin M4 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20150618 MGI PMID:24339795 1313680 Cnnm4 cyclin M4 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20210429 MGI PMID:28033128 1313680 Cnnm4 cyclin M4 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20210429 MGI PMID:28033128 1313680 Cnnm4 cyclin M4 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20150618 MGI PMID:24339795 1313680 Cnnm4 cyclin M4 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20150618 MGI PMID:24339795 1313680 Cnnm4 cyclin M4 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20210429 MGI PMID:28033128 1313680 Cnnm4 cyclin M4 gene MP:0011436 decreased urine magnesium level IAGP N RGD:5509061 20150618 MGI PMID:24339795 1313680 Cnnm4 cyclin M4 gene MP:0013129 abnormal tooth color IAGP N RGD:5509061 20150618 MGI PMID:24339795 1313680 Cnnm4 cyclin M4 gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20171221 MGI PMID:24339795 1313683 Rpl38 ribosomal protein L38 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:21062742 1313683 Rpl38 ribosomal protein L38 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10889952 1313683 Rpl38 ribosomal protein L38 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0000154 rib fusion IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0000267 abnormal heart development IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:21062742 1313683 Rpl38 ribosomal protein L38 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:10889952 1313683 Rpl38 ribosomal protein L38 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:10889952 1313683 Rpl38 ribosomal protein L38 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:10889952 1313683 Rpl38 ribosomal protein L38 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:10889952 1313683 Rpl38 ribosomal protein L38 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:21062742 1313683 Rpl38 ribosomal protein L38 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:465735 1313683 Rpl38 ribosomal protein L38 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:9615218 1313683 Rpl38 ribosomal protein L38 gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:10889952 1313683 Rpl38 ribosomal protein L38 gene MP:0000819 abnormal olfactory bulb morphology IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10889952 1313683 Rpl38 ribosomal protein L38 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0000930 wavy neural tube IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21062742 1313683 Rpl38 ribosomal protein L38 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:21062742 1313683 Rpl38 ribosomal protein L38 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7373273 1313683 Rpl38 ribosomal protein L38 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:7373273 1313683 Rpl38 ribosomal protein L38 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:21062742 1313683 Rpl38 ribosomal protein L38 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:465735 1313683 Rpl38 ribosomal protein L38 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:21062742 1313683 Rpl38 ribosomal protein L38 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:10889952 1313683 Rpl38 ribosomal protein L38 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0002237 abnormal nasal cavity morphology IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:7373273 1313683 Rpl38 ribosomal protein L38 gene MP:0002764 short tibia IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:2980249 1313683 Rpl38 ribosomal protein L38 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0003050 abnormal sacral vertebrae morphology IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:10889952 1313683 Rpl38 ribosomal protein L38 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:465735 1313683 Rpl38 ribosomal protein L38 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0003072 abnormal metatarsal bone morphology IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0003073 abnormal metacarpal bone morphology IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0003109 short femur IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0003208 abnormal neuromere morphology IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0003330 abnormal auditory tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21062742 1313683 Rpl38 ribosomal protein L38 gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:465735 1313683 Rpl38 ribosomal protein L38 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7373273 1313683 Rpl38 ribosomal protein L38 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:465735 1313683 Rpl38 ribosomal protein L38 gene MP:0004322 abnormal sternebra morphology IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0004351 short humerus IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0004355 short radius IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0004479 abnormal oval window morphology IAGP N RGD:5509061 20141003 MGI PMID:21062742 1313683 Rpl38 ribosomal protein L38 gene MP:0004480 abnormal round window morphology IAGP N RGD:5509061 20141003 MGI PMID:21062742 1313683 Rpl38 ribosomal protein L38 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0004600 abnormal vertebral transverse process morphology IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0004604 abnormal vertebral pedicle morphology IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0004605 abnormal vertebral lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0004614 caudal vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0004651 increased thoracic vertebrae number IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0004652 small caudal vertebrae IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0004653 absent caudal vertebrae IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0004686 decreased length of long bones IEA N RGD:5509061 20141003 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:21062742 1313683 Rpl38 ribosomal protein L38 gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20141003 MGI PMID:21062742 1313683 Rpl38 ribosomal protein L38 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:7373273 1313683 Rpl38 ribosomal protein L38 gene MP:0004963 abnormal blastocoele morphology IAGP N RGD:5509061 20141003 MGI PMID:7373273 1313683 Rpl38 ribosomal protein L38 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:10889952 1313683 Rpl38 ribosomal protein L38 gene MP:0005225 abnormal vertebrae development IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20111116 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19011615 1313683 Rpl38 ribosomal protein L38 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0008830 abnormal nucleolus morphology IAGP N RGD:5509061 20141003 MGI PMID:7373273 1313683 Rpl38 ribosomal protein L38 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:7373273 1313683 Rpl38 ribosomal protein L38 gene MP:0010082 sternebra fusion IEA N RGD:5509061 20141003 MGI 1313683 Rpl38 ribosomal protein L38 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9615218 1313683 Rpl38 ribosomal protein L38 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10889952 1313683 Rpl38 ribosomal protein L38 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14779008 1313683 Rpl38 ribosomal protein L38 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8995757 1313683 Rpl38 ribosomal protein L38 gene MP:0011103 embryonic lethality at implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7373273 1313683 Rpl38 ribosomal protein L38 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21062742 1313683 Rpl38 ribosomal protein L38 gene MP:0012284 increased sternebra number IEA N RGD:5509061 20141003 MGI 1313684 Polr3a polymerase (RNA) III (DNA directed) polypeptide A gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220811 MGI 1313684 Polr3a polymerase (RNA) III (DNA directed) polypeptide A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:28407788 1313684 Polr3a polymerase (RNA) III (DNA directed) polypeptide A gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20220811 MGI 1313684 Polr3a polymerase (RNA) III (DNA directed) polypeptide A gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1313684 Polr3a polymerase (RNA) III (DNA directed) polypeptide A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28407788 1313684 Polr3a polymerase (RNA) III (DNA directed) polypeptide A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1313684 Polr3a polymerase (RNA) III (DNA directed) polypeptide A gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220811 MGI 1313684 Polr3a polymerase (RNA) III (DNA directed) polypeptide A gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220811 MGI 1313684 Polr3a polymerase (RNA) III (DNA directed) polypeptide A gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220811 MGI 1313688 Kif9 kinesin family member 9 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1313688 Kif9 kinesin family member 9 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1313688 Kif9 kinesin family member 9 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1313688 Kif9 kinesin family member 9 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20211209 MGI PMID:32072696 1313688 Kif9 kinesin family member 9 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1313688 Kif9 kinesin family member 9 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 1313688 Kif9 kinesin family member 9 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20211209 MGI PMID:32072696 1313688 Kif9 kinesin family member 9 gene MP:0009084 blind uterus IEA N RGD:5509061 20210520 MGI 1313688 Kif9 kinesin family member 9 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20211209 MGI PMID:32072696 1313688 Kif9 kinesin family member 9 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20211209 MGI PMID:32072696 1313688 Kif9 kinesin family member 9 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20211209 MGI PMID:32072696 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17008428 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17717065 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20838603 1313690 Mcm2 minichromosome maintenance complex component 2 gene MP:0014127 increased thymoma incidence IAGP N RGD:5509061 20160317 MGI PMID:17717065 1313692 Swap70 SWA-70 protein gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:11500831 1313692 Swap70 SWA-70 protein gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11500831 1313692 Swap70 SWA-70 protein gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:11500831 1313692 Swap70 SWA-70 protein gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:11500831 1313695 Itgb2 integrin beta 2 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:16172402 1313695 Itgb2 integrin beta 2 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:16172402 1313695 Itgb2 integrin beta 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10528208 1313695 Itgb2 integrin beta 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8101543 1313695 Itgb2 integrin beta 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10228023 1313695 Itgb2 integrin beta 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10528208 1313695 Itgb2 integrin beta 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23823319 1313695 Itgb2 integrin beta 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10528208 1313695 Itgb2 integrin beta 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20181011 MGI 1313695 Itgb2 integrin beta 2 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:8101543 1313695 Itgb2 integrin beta 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12819024 1313695 Itgb2 integrin beta 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:14634077 1313695 Itgb2 integrin beta 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23823319 1313695 Itgb2 integrin beta 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:12819024 1313695 Itgb2 integrin beta 2 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:12819024 1313695 Itgb2 integrin beta 2 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:14634077 1313695 Itgb2 integrin beta 2 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:12819024 1313695 Itgb2 integrin beta 2 gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:14634077 1313695 Itgb2 integrin beta 2 gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:16982899 1313695 Itgb2 integrin beta 2 gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:18390736 1313695 Itgb2 integrin beta 2 gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:12819024 1313695 Itgb2 integrin beta 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:14634077 1313695 Itgb2 integrin beta 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:10228023 1313695 Itgb2 integrin beta 2 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:12819024 1313695 Itgb2 integrin beta 2 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:12766082 1313695 Itgb2 integrin beta 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:15231732 1313695 Itgb2 integrin beta 2 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20200116 MGI PMID:16505059 1313695 Itgb2 integrin beta 2 gene MP:0001805 decreased IgG level IEA N RGD:5509061 20181011 MGI 1313695 Itgb2 integrin beta 2 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:14634077 1313695 Itgb2 integrin beta 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:12819024 1313695 Itgb2 integrin beta 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:8101543 1313695 Itgb2 integrin beta 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15231732 1313695 Itgb2 integrin beta 2 gene MP:0002145 abnormal T cell differentiation IEA N RGD:5509061 20190418 MGI 1313695 Itgb2 integrin beta 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22711877 1313695 Itgb2 integrin beta 2 gene MP:0002221 abnormal lymph organ size IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:8101543 1313695 Itgb2 integrin beta 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18451854 1313695 Itgb2 integrin beta 2 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15585877 1313695 Itgb2 integrin beta 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23823319 1313695 Itgb2 integrin beta 2 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0002497 increased IgE level IEA N RGD:5509061 20181011 MGI 1313695 Itgb2 integrin beta 2 gene MP:0002606 increased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15231732 1313695 Itgb2 integrin beta 2 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:10528208 1313695 Itgb2 integrin beta 2 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:12819024 1313695 Itgb2 integrin beta 2 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0003434 decreased susceptibility to induced choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:12766082 1313695 Itgb2 integrin beta 2 gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20141003 MGI PMID:18390736 1313695 Itgb2 integrin beta 2 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:10528208 1313695 Itgb2 integrin beta 2 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16172402 1313695 Itgb2 integrin beta 2 gene MP:0003813 abnormal hair follicle dermal papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0003884 decreased macrophage cell number IEA N RGD:5509061 20181011 MGI 1313695 Itgb2 integrin beta 2 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10528208 1313695 Itgb2 integrin beta 2 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10528208 1313695 Itgb2 integrin beta 2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8101543 1313695 Itgb2 integrin beta 2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23823319 1313695 Itgb2 integrin beta 2 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:14634077 1313695 Itgb2 integrin beta 2 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23823319 1313695 Itgb2 integrin beta 2 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20181011 MGI 1313695 Itgb2 integrin beta 2 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IEA N RGD:5509061 20181011 MGI 1313695 Itgb2 integrin beta 2 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:10228023 1313695 Itgb2 integrin beta 2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1313695 Itgb2 integrin beta 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1313695 Itgb2 integrin beta 2 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15210787 1313695 Itgb2 integrin beta 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23823319 1313695 Itgb2 integrin beta 2 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:15231732 1313695 Itgb2 integrin beta 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15231732 1313695 Itgb2 integrin beta 2 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:14634077 1313695 Itgb2 integrin beta 2 gene MP:0008039 increased NK T cell number IEA N RGD:5509061 20181011 MGI 1313695 Itgb2 integrin beta 2 gene MP:0008053 abnormal NK cell differentiation IEA N RGD:5509061 20111116 MGI 1313695 Itgb2 integrin beta 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1313695 Itgb2 integrin beta 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1313695 Itgb2 integrin beta 2 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1313695 Itgb2 integrin beta 2 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:14634077 1313695 Itgb2 integrin beta 2 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23823319 1313695 Itgb2 integrin beta 2 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23823319 1313695 Itgb2 integrin beta 2 gene MP:0008127 decreased dendritic cell number IEA N RGD:5509061 20181011 MGI 1313695 Itgb2 integrin beta 2 gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20190418 MGI 1313695 Itgb2 integrin beta 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200116 MGI PMID:16505059 1313695 Itgb2 integrin beta 2 gene MP:0008564 increased interferon-beta secretion IEA N RGD:5509061 20181011 MGI 1313695 Itgb2 integrin beta 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:14634077 1313695 Itgb2 integrin beta 2 gene MP:0008567 decreased interferon-gamma secretion IEA N RGD:5509061 20111116 MGI 1313695 Itgb2 integrin beta 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0008623 increased circulating interleukin-3 level IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:14634077 1313695 Itgb2 integrin beta 2 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:10228023 1313695 Itgb2 integrin beta 2 gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20141003 MGI PMID:12819024 1313695 Itgb2 integrin beta 2 gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:18451854 1313695 Itgb2 integrin beta 2 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8101543 1313695 Itgb2 integrin beta 2 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8700894 1313695 Itgb2 integrin beta 2 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1313695 Itgb2 integrin beta 2 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:16172402 1313695 Itgb2 integrin beta 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9653089 1313695 Itgb2 integrin beta 2 gene MP:0013280 abnormal cytotoxic T cell cytolysis IEA N RGD:5509061 20181011 MGI 1313695 Itgb2 integrin beta 2 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:16172402 1313695 Itgb2 integrin beta 2 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:16172402 1313695 Itgb2 integrin beta 2 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:16172402 1313695 Itgb2 integrin beta 2 gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20181011 MGI 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0001128 ovary hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0006361 abnormal female germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:21987787 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22771120 1313697 Mcm9 minichromosome maintenance 9 homologous recombination repair factor gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20200130 MGI PMID:21987787 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20150122 MGI PMID:24733397 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20150122 MGI PMID:24733397 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20150122 MGI PMID:24733397 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0001785 edema IAGP N RGD:5509061 20150122 MGI PMID:24733397 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0003889 enhanced sensorimotor gating IEA N RGD:5509061 20141003 MGI 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0005444 abnormal retinol metabolism IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0005444 abnormal retinol metabolism IAGP N RGD:5509061 20150122 MGI PMID:24733397 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20150122 MGI PMID:24733397 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20150122 MGI PMID:24733397 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24005908 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 1313700 Dhrs3 dehydrogenase/reductase 3 gene MP:0011234 abnormal retinol level IAGP N RGD:5509061 20150122 MGI PMID:24733397 1313702 Col6a2 collagen, type VI, alpha 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20180215 MGI 1313702 Col6a2 collagen, type VI, alpha 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160114 MGI 1313707 Rag2 recombination activating gene 2 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10614672 1313707 Rag2 recombination activating gene 2 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12871643 1313707 Rag2 recombination activating gene 2 gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:11602643 1313707 Rag2 recombination activating gene 2 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:10614672 1313707 Rag2 recombination activating gene 2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:12871643 1313707 Rag2 recombination activating gene 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11884426 1313707 Rag2 recombination activating gene 2 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17923086 1313707 Rag2 recombination activating gene 2 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7595226 1313707 Rag2 recombination activating gene 2 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:17923086 1313707 Rag2 recombination activating gene 2 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:7595226 1313707 Rag2 recombination activating gene 2 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10982764 1313707 Rag2 recombination activating gene 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19283781 1313707 Rag2 recombination activating gene 2 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:12618483 1313707 Rag2 recombination activating gene 2 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10843678 1313707 Rag2 recombination activating gene 2 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20937703 1313707 Rag2 recombination activating gene 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10523604 1313707 Rag2 recombination activating gene 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:12618483 1313707 Rag2 recombination activating gene 2 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12531919 1313707 Rag2 recombination activating gene 2 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:17442925 1313707 Rag2 recombination activating gene 2 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:10610182 1313707 Rag2 recombination activating gene 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:10610182 1313707 Rag2 recombination activating gene 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20151217 MGI PMID:26099023 1313707 Rag2 recombination activating gene 2 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20151217 MGI PMID:26099023 1313707 Rag2 recombination activating gene 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10614672 1313707 Rag2 recombination activating gene 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20151112 MGI PMID:22089030 1313707 Rag2 recombination activating gene 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18676849 1313707 Rag2 recombination activating gene 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:7595226 1313707 Rag2 recombination activating gene 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7595226 1313707 Rag2 recombination activating gene 2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17923086 1313707 Rag2 recombination activating gene 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17515402 1313707 Rag2 recombination activating gene 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:21791433 1313707 Rag2 recombination activating gene 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:23661644 1313707 Rag2 recombination activating gene 2 gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20141003 MGI 1313707 Rag2 recombination activating gene 2 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11602643 1313707 Rag2 recombination activating gene 2 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12531919 1313707 Rag2 recombination activating gene 2 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12618483 1313707 Rag2 recombination activating gene 2 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12531919 1313707 Rag2 recombination activating gene 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19283781 1313707 Rag2 recombination activating gene 2 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11602643 1313707 Rag2 recombination activating gene 2 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12531919 1313707 Rag2 recombination activating gene 2 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12618483 1313707 Rag2 recombination activating gene 2 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15197172 1313707 Rag2 recombination activating gene 2 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19597497 1313707 Rag2 recombination activating gene 2 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9341770 1313707 Rag2 recombination activating gene 2 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:9285410 1313707 Rag2 recombination activating gene 2 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:24021673 1313707 Rag2 recombination activating gene 2 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:10610182 1313707 Rag2 recombination activating gene 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17082625 1313707 Rag2 recombination activating gene 2 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20160505 MGI PMID:22264274 1313707 Rag2 recombination activating gene 2 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21349429 1313707 Rag2 recombination activating gene 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21349429 1313707 Rag2 recombination activating gene 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21368836 1313707 Rag2 recombination activating gene 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9584189 1313707 Rag2 recombination activating gene 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20161222 MGI PMID:26753883 1313707 Rag2 recombination activating gene 2 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20161222 MGI PMID:26753883 1313707 Rag2 recombination activating gene 2 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16397239 1313707 Rag2 recombination activating gene 2 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:17908936 1313707 Rag2 recombination activating gene 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21368836 1313707 Rag2 recombination activating gene 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9584189 1313707 Rag2 recombination activating gene 2 gene MP:0002083 premature death IAGP N RGD:5509061 20151217 MGI PMID:26099023 1313707 Rag2 recombination activating gene 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12871643 1313707 Rag2 recombination activating gene 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16186486 1313707 Rag2 recombination activating gene 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15238603 1313707 Rag2 recombination activating gene 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18776904 1313707 Rag2 recombination activating gene 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20937703 1313707 Rag2 recombination activating gene 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21746917 1313707 Rag2 recombination activating gene 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10485655 1313707 Rag2 recombination activating gene 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11602643 1313707 Rag2 recombination activating gene 2 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12433370 1313707 Rag2 recombination activating gene 2 gene MP:0002403 abnormal pre-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12433370 1313707 Rag2 recombination activating gene 2 gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15021880 1313707 Rag2 recombination activating gene 2 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17617584 1313707 Rag2 recombination activating gene 2 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15021880 1313707 Rag2 recombination activating gene 2 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17579027 1313707 Rag2 recombination activating gene 2 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9285410 1313707 Rag2 recombination activating gene 2 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17082625 1313707 Rag2 recombination activating gene 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17082625 1313707 Rag2 recombination activating gene 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:19084435 1313707 Rag2 recombination activating gene 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20951970 1313707 Rag2 recombination activating gene 2 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:7595226 1313707 Rag2 recombination activating gene 2 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9285410 1313707 Rag2 recombination activating gene 2 gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11239447 1313707 Rag2 recombination activating gene 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18539897 1313707 Rag2 recombination activating gene 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17082625 1313707 Rag2 recombination activating gene 2 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:12531919 1313707 Rag2 recombination activating gene 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12871643 1313707 Rag2 recombination activating gene 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20170824 MGI PMID:25398911 1313707 Rag2 recombination activating gene 2 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20151217 MGI PMID:26099023 1313707 Rag2 recombination activating gene 2 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:17081782 1313707 Rag2 recombination activating gene 2 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:17923086 1313707 Rag2 recombination activating gene 2 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:7595226 1313707 Rag2 recombination activating gene 2 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11239447 1313707 Rag2 recombination activating gene 2 gene MP:0003080 increased natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17515402 1313707 Rag2 recombination activating gene 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21262827 1313707 Rag2 recombination activating gene 2 gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7595226 1313707 Rag2 recombination activating gene 2 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:17923086 1313707 Rag2 recombination activating gene 2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20161222 MGI PMID:26753883 1313707 Rag2 recombination activating gene 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:18676849 1313707 Rag2 recombination activating gene 2 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:18676849 1313707 Rag2 recombination activating gene 2 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7595226 1313707 Rag2 recombination activating gene 2 gene MP:0003454 erythroderma IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0003504 thyroid gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:9285410 1313707 Rag2 recombination activating gene 2 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:16087873 1313707 Rag2 recombination activating gene 2 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:21368836 1313707 Rag2 recombination activating gene 2 gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:17442925 1313707 Rag2 recombination activating gene 2 gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:17641034 1313707 Rag2 recombination activating gene 2 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15383179 1313707 Rag2 recombination activating gene 2 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:21368836 1313707 Rag2 recombination activating gene 2 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:19587764 1313707 Rag2 recombination activating gene 2 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17873878 1313707 Rag2 recombination activating gene 2 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:19483694 1313707 Rag2 recombination activating gene 2 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:19587764 1313707 Rag2 recombination activating gene 2 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17923086 1313707 Rag2 recombination activating gene 2 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20151112 MGI PMID:22089030 1313707 Rag2 recombination activating gene 2 gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:10614672 1313707 Rag2 recombination activating gene 2 gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:10843678 1313707 Rag2 recombination activating gene 2 gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:19283781 1313707 Rag2 recombination activating gene 2 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11751756 1313707 Rag2 recombination activating gene 2 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17873878 1313707 Rag2 recombination activating gene 2 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20170824 MGI PMID:25398911 1313707 Rag2 recombination activating gene 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24021673 1313707 Rag2 recombination activating gene 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12618483 1313707 Rag2 recombination activating gene 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12871643 1313707 Rag2 recombination activating gene 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:15021880 1313707 Rag2 recombination activating gene 2 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9164958 1313707 Rag2 recombination activating gene 2 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:7595226 1313707 Rag2 recombination activating gene 2 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11163198 1313707 Rag2 recombination activating gene 2 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9341770 1313707 Rag2 recombination activating gene 2 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:11751756 1313707 Rag2 recombination activating gene 2 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12531919 1313707 Rag2 recombination activating gene 2 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:15197172 1313707 Rag2 recombination activating gene 2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:15197172 1313707 Rag2 recombination activating gene 2 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10843678 1313707 Rag2 recombination activating gene 2 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442925 1313707 Rag2 recombination activating gene 2 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17617584 1313707 Rag2 recombination activating gene 2 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597497 1313707 Rag2 recombination activating gene 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12618483 1313707 Rag2 recombination activating gene 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18923423 1313707 Rag2 recombination activating gene 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19283781 1313707 Rag2 recombination activating gene 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22653054 1313707 Rag2 recombination activating gene 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9285410 1313707 Rag2 recombination activating gene 2 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9285410 1313707 Rag2 recombination activating gene 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17641034 1313707 Rag2 recombination activating gene 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21746917 1313707 Rag2 recombination activating gene 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:7595226 1313707 Rag2 recombination activating gene 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10614672 1313707 Rag2 recombination activating gene 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14706337 1313707 Rag2 recombination activating gene 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9341770 1313707 Rag2 recombination activating gene 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9285410 1313707 Rag2 recombination activating gene 2 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:17081782 1313707 Rag2 recombination activating gene 2 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:15383179 1313707 Rag2 recombination activating gene 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12498815 1313707 Rag2 recombination activating gene 2 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:20937871 1313707 Rag2 recombination activating gene 2 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:17081782 1313707 Rag2 recombination activating gene 2 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:20951970 1313707 Rag2 recombination activating gene 2 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:21262803 1313707 Rag2 recombination activating gene 2 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:21262827 1313707 Rag2 recombination activating gene 2 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141211 MGI PMID:24633240 1313707 Rag2 recombination activating gene 2 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20210506 MGI PMID:32381589 1313707 Rag2 recombination activating gene 2 gene MP:0005673 decreased susceptibility to graft versus host disease IAGP N RGD:5509061 20141003 MGI PMID:24021673 1313707 Rag2 recombination activating gene 2 gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:10610182 1313707 Rag2 recombination activating gene 2 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:17363300 1313707 Rag2 recombination activating gene 2 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15021880 1313707 Rag2 recombination activating gene 2 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:12586624 1313707 Rag2 recombination activating gene 2 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19084435 1313707 Rag2 recombination activating gene 2 gene MP:0008046 absent NK cells IAGP N RGD:5509061 20141003 MGI PMID:12586624 1313707 Rag2 recombination activating gene 2 gene MP:0008046 absent NK cells IAGP N RGD:5509061 20141003 MGI PMID:17082625 1313707 Rag2 recombination activating gene 2 gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:12586624 1313707 Rag2 recombination activating gene 2 gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:17082625 1313707 Rag2 recombination activating gene 2 gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:12586624 1313707 Rag2 recombination activating gene 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17918199 1313707 Rag2 recombination activating gene 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10843678 1313707 Rag2 recombination activating gene 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17617584 1313707 Rag2 recombination activating gene 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19283781 1313707 Rag2 recombination activating gene 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24021673 1313707 Rag2 recombination activating gene 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9285410 1313707 Rag2 recombination activating gene 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9341770 1313707 Rag2 recombination activating gene 2 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10843678 1313707 Rag2 recombination activating gene 2 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17918199 1313707 Rag2 recombination activating gene 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17617584 1313707 Rag2 recombination activating gene 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24021673 1313707 Rag2 recombination activating gene 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9341770 1313707 Rag2 recombination activating gene 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9341770 1313707 Rag2 recombination activating gene 2 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19283781 1313707 Rag2 recombination activating gene 2 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597497 1313707 Rag2 recombination activating gene 2 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:11602643 1313707 Rag2 recombination activating gene 2 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19283781 1313707 Rag2 recombination activating gene 2 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:11602643 1313707 Rag2 recombination activating gene 2 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:11602643 1313707 Rag2 recombination activating gene 2 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20151224 MGI PMID:24509509 1313707 Rag2 recombination activating gene 2 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12433370 1313707 Rag2 recombination activating gene 2 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12531919 1313707 Rag2 recombination activating gene 2 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12871643 1313707 Rag2 recombination activating gene 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11602643 1313707 Rag2 recombination activating gene 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12531919 1313707 Rag2 recombination activating gene 2 gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0008213 absent immature B cells IAGP N RGD:5509061 20141003 MGI PMID:11602643 1313707 Rag2 recombination activating gene 2 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12531919 1313707 Rag2 recombination activating gene 2 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12531919 1313707 Rag2 recombination activating gene 2 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:11602643 1313707 Rag2 recombination activating gene 2 gene MP:0008348 absent gamma-delta T cells IAGP N RGD:5509061 20141003 MGI PMID:17617584 1313707 Rag2 recombination activating gene 2 gene MP:0008356 abnormal gamma-delta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12531919 1313707 Rag2 recombination activating gene 2 gene MP:0008464 absent peripheral lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:24021673 1313707 Rag2 recombination activating gene 2 gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7595226 1313707 Rag2 recombination activating gene 2 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20141003 MGI PMID:17082625 1313707 Rag2 recombination activating gene 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17923086 1313707 Rag2 recombination activating gene 2 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:19084435 1313707 Rag2 recombination activating gene 2 gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20151112 MGI PMID:22089030 1313707 Rag2 recombination activating gene 2 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20151112 MGI PMID:22089030 1313707 Rag2 recombination activating gene 2 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17641034 1313707 Rag2 recombination activating gene 2 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17082625 1313707 Rag2 recombination activating gene 2 gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0008755 abnormal immunoglobulin V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:1547487 1313707 Rag2 recombination activating gene 2 gene MP:0008755 abnormal immunoglobulin V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:21349429 1313707 Rag2 recombination activating gene 2 gene MP:0008759 abnormal T cell receptor delta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:17579065 1313707 Rag2 recombination activating gene 2 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:9285410 1313707 Rag2 recombination activating gene 2 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20937703 1313707 Rag2 recombination activating gene 2 gene MP:0009515 increased gastrointestinal stromal tumor incidence IAGP N RGD:5509061 20161222 MGI PMID:26753883 1313707 Rag2 recombination activating gene 2 gene MP:0009540 absent Hassall's corpuscle IAGP N RGD:5509061 20141003 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0009624 small inguinal lymph nodes IAGP N RGD:5509061 20170713 MGI PMID:17476358 1313707 Rag2 recombination activating gene 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17082625 1313707 Rag2 recombination activating gene 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20639491 1313707 Rag2 recombination activating gene 2 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17082625 1313707 Rag2 recombination activating gene 2 gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:12433370 1313707 Rag2 recombination activating gene 2 gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20161222 MGI PMID:26753883 1313707 Rag2 recombination activating gene 2 gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:17363300 1313707 Rag2 recombination activating gene 2 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20160505 MGI PMID:22264274 1313707 Rag2 recombination activating gene 2 gene MP:0010365 increased thymus tumor incidence IAGP N RGD:5509061 20161222 MGI PMID:26753883 1313707 Rag2 recombination activating gene 2 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10982764 1313707 Rag2 recombination activating gene 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20190207 MGI PMID:26880576 1313707 Rag2 recombination activating gene 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21368836 1313707 Rag2 recombination activating gene 2 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:22089030 1313707 Rag2 recombination activating gene 2 gene MP:0020184 abnormal susceptibility to parasitic infection IAGP N RGD:5509061 20170824 MGI PMID:25398911 1313707 Rag2 recombination activating gene 2 gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:24021673 1313707 Rag2 recombination activating gene 2 gene MP:0030011 small cervical lymph nodes IAGP N RGD:5509061 20170713 MGI PMID:17476358 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0000601 small liver IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0001147 small testis IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230601 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20230601 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0002833 increased heart weight IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20150716 MGI PMID:24958848 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20230119 MGI 1313709 Fgd5 FYVE, RhoGEF and PH domain containing 5 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20141003 MGI 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20220908 MGI PMID:33964306 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0001191 abnormal skin condition IEA N RGD:5509061 20160804 MGI 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20160804 MGI 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20220908 MGI PMID:33964306 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20160804 MGI 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0002791 steatorrhea IAGP N RGD:5509061 20220908 MGI PMID:33964306 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20220908 MGI PMID:33964306 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20220908 MGI PMID:33964306 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20220908 MGI PMID:33964306 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20220908 MGI PMID:33964306 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20220908 MGI PMID:33964306 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20220908 MGI PMID:33964306 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0020151 abnormal circulating non-HDL cholesterol level IAGP N RGD:5509061 20220908 MGI PMID:33964306 1313711 Sar1b secretion associated Ras related GTPase 1B gene MP:0020868 decreased lipogenesis IAGP N RGD:5509061 20220908 MGI PMID:33964306 1313713 Slc37a2 solute carrier family 37 (glycerol-3-phosphate transporter), member 2 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20240523 MGI 1313713 Slc37a2 solute carrier family 37 (glycerol-3-phosphate transporter), member 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1313713 Slc37a2 solute carrier family 37 (glycerol-3-phosphate transporter), member 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1313713 Slc37a2 solute carrier family 37 (glycerol-3-phosphate transporter), member 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1313713 Slc37a2 solute carrier family 37 (glycerol-3-phosphate transporter), member 2 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 1313713 Slc37a2 solute carrier family 37 (glycerol-3-phosphate transporter), member 2 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1313713 Slc37a2 solute carrier family 37 (glycerol-3-phosphate transporter), member 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230119 MGI 1313713 Slc37a2 solute carrier family 37 (glycerol-3-phosphate transporter), member 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20211021 MGI PMID:32428862 1313713 Slc37a2 solute carrier family 37 (glycerol-3-phosphate transporter), member 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1313713 Slc37a2 solute carrier family 37 (glycerol-3-phosphate transporter), member 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20211021 MGI PMID:32428862 1313713 Slc37a2 solute carrier family 37 (glycerol-3-phosphate transporter), member 2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20211021 MGI PMID:32428862 1313713 Slc37a2 solute carrier family 37 (glycerol-3-phosphate transporter), member 2 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20211021 MGI PMID:32428862 1313713 Slc37a2 solute carrier family 37 (glycerol-3-phosphate transporter), member 2 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20211021 MGI PMID:32428862 1313713 Slc37a2 solute carrier family 37 (glycerol-3-phosphate transporter), member 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20240523 MGI 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0003794 delayed somite formation IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0003891 increased allantois apoptosis IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0004559 small allantois IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0011200 abnormal extraembryonic coelom morphology IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0020515 abnormal visceral yolk sac endoderm morphology IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313714 Pagr1a PAXIP1 associated glutamate rich protein 1A gene MP:0020517 abnormal visceral yolk sac physiology IAGP N RGD:5509061 20180712 MGI PMID:24633704 1313716 Evx2 even-skipped homeobox 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:8978698 1313716 Evx2 even-skipped homeobox 2 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:8674109 1313716 Evx2 even-skipped homeobox 2 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8674109 1313716 Evx2 even-skipped homeobox 2 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8978698 1313716 Evx2 even-skipped homeobox 2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:8978698 1313716 Evx2 even-skipped homeobox 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8978698 1313716 Evx2 even-skipped homeobox 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8978698 1313716 Evx2 even-skipped homeobox 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8978698 1313716 Evx2 even-skipped homeobox 2 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:8978698 1313716 Evx2 even-skipped homeobox 2 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:8674109 1313716 Evx2 even-skipped homeobox 2 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:8978698 1313716 Evx2 even-skipped homeobox 2 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:8674109 1313716 Evx2 even-skipped homeobox 2 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8978698 1313716 Evx2 even-skipped homeobox 2 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:8674109 1313716 Evx2 even-skipped homeobox 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:8674109 1313716 Evx2 even-skipped homeobox 2 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20141003 MGI PMID:8674109 1313716 Evx2 even-skipped homeobox 2 gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:8674109 1313716 Evx2 even-skipped homeobox 2 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:8978698 1313716 Evx2 even-skipped homeobox 2 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8978698 1313716 Evx2 even-skipped homeobox 2 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:8978698 1313718 Adgre5 adhesion G protein-coupled receptor E5 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:17158902 1313718 Adgre5 adhesion G protein-coupled receptor E5 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18941248 1313718 Adgre5 adhesion G protein-coupled receptor E5 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1313718 Adgre5 adhesion G protein-coupled receptor E5 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17158902 1313718 Adgre5 adhesion G protein-coupled receptor E5 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17158902 1313722 Gba2 glucosidase beta 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17080196 1313722 Gba2 glucosidase beta 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:17080196 1313722 Gba2 glucosidase beta 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17080196 1313722 Gba2 glucosidase beta 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17080196 1313722 Gba2 glucosidase beta 2 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17080196 1313722 Gba2 glucosidase beta 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17080196 1313722 Gba2 glucosidase beta 2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17080196 1313722 Gba2 glucosidase beta 2 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20160804 MGI 1313722 Gba2 glucosidase beta 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17080196 1313722 Gba2 glucosidase beta 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17080196 1313722 Gba2 glucosidase beta 2 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17080196 1313722 Gba2 glucosidase beta 2 gene MP:0009257 dilated seminiferous tubule IAGP N RGD:5509061 20220922 MGI PMID:17080196 1313722 Gba2 glucosidase beta 2 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:17080196 1313724 U2af1l4 U2 small nuclear RNA auxiliary factor 1-like 4 gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:24837677 1313728 Ephb3 Eph receptor B3 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:10839360 1313728 Ephb3 Eph receptor B3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21539827 1313728 Ephb3 Eph receptor B3 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:23143520 1313728 Ephb3 Eph receptor B3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:10839360 1313728 Ephb3 Eph receptor B3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10839360 1313728 Ephb3 Eph receptor B3 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:19914164 1313728 Ephb3 Eph receptor B3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10839360 1313728 Ephb3 Eph receptor B3 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:12971893 1313728 Ephb3 Eph receptor B3 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:10839360 1313728 Ephb3 Eph receptor B3 gene MP:0002946 delayed axon extension IAGP N RGD:5509061 20141003 MGI PMID:10839360 1313728 Ephb3 Eph receptor B3 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:10839360 1313728 Ephb3 Eph receptor B3 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:21539827 1313728 Ephb3 Eph receptor B3 gene MP:0003124 hypospadia IAGP N RGD:5509061 20141003 MGI PMID:15223334 1313728 Ephb3 Eph receptor B3 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:23143520 1313728 Ephb3 Eph receptor B3 gene MP:0004267 abnormal optic tract morphology IAGP N RGD:5509061 20141003 MGI PMID:12971893 1313728 Ephb3 Eph receptor B3 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:10839360 1313728 Ephb3 Eph receptor B3 gene MP:0004775 abnormal vestibular dark cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10839360 1313728 Ephb3 Eph receptor B3 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:16777604 1313728 Ephb3 Eph receptor B3 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16777604 1313728 Ephb3 Eph receptor B3 gene MP:0004885 abnormal endolymph physiology IAGP N RGD:5509061 20141003 MGI PMID:17158005 1313728 Ephb3 Eph receptor B3 gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20141003 MGI PMID:15223334 1313728 Ephb3 Eph receptor B3 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19182796 1313728 Ephb3 Eph receptor B3 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:21847105 1313728 Ephb3 Eph receptor B3 gene MP:0006389 abnormal vestibular endolymph physiology IAGP N RGD:5509061 20141003 MGI PMID:17158005 1313728 Ephb3 Eph receptor B3 gene MP:0006391 abnormal vestibular endolymph ionic homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17158005 1313728 Ephb3 Eph receptor B3 gene MP:0008066 small endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:10839360 1313728 Ephb3 Eph receptor B3 gene MP:0008960 abnormal axon pruning IAGP N RGD:5509061 20141003 MGI PMID:19182796 1313728 Ephb3 Eph receptor B3 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19914164 1313728 Ephb3 Eph receptor B3 gene MP:0014077 ectopic Paneth cells IAGP N RGD:5509061 20160310 MGI PMID:19914164 1313730 Pfdn1 prefoldin 1 gene MP:0000111 cleft palate IEA N RGD:5509061 20210520 MGI 1313730 Pfdn1 prefoldin 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20220811 MGI 1313730 Pfdn1 prefoldin 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1313730 Pfdn1 prefoldin 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20220811 MGI 1313730 Pfdn1 prefoldin 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210128 MGI 1313730 Pfdn1 prefoldin 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0001872 sinus inflammation IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1313730 Pfdn1 prefoldin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20210128 MGI 1313730 Pfdn1 prefoldin 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:18566413 1313730 Pfdn1 prefoldin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1313731 Ccdc30 coiled-coil domain containing 30 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1313734 Otud4 OTU domain containing 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1313736 Adamtsl5 ADAMTS-like 5 gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 1313738 Adgrb1 adhesion G protein-coupled receptor B1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20141003 MGI 1313738 Adgrb1 adhesion G protein-coupled receptor B1 gene MP:0001413 abnormal response to new environment IEA N RGD:5509061 20200402 MGI 1313738 Adgrb1 adhesion G protein-coupled receptor B1 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20201015 MGI PMID:25751059 1313738 Adgrb1 adhesion G protein-coupled receptor B1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20201015 MGI PMID:25751059 1313738 Adgrb1 adhesion G protein-coupled receptor B1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20201015 MGI PMID:25751059 1313738 Adgrb1 adhesion G protein-coupled receptor B1 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1313738 Adgrb1 adhesion G protein-coupled receptor B1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20201015 MGI PMID:25751059 1313738 Adgrb1 adhesion G protein-coupled receptor B1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20150625 MGI 1313738 Adgrb1 adhesion G protein-coupled receptor B1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1313738 Adgrb1 adhesion G protein-coupled receptor B1 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20201015 MGI PMID:25751059 1313738 Adgrb1 adhesion G protein-coupled receptor B1 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20201015 MGI PMID:25751059 1313738 Adgrb1 adhesion G protein-coupled receptor B1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20201015 MGI PMID:25751059 1313738 Adgrb1 adhesion G protein-coupled receptor B1 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20201015 MGI PMID:25751059 1313740 Shcbp1l Shc SH2-domain binding protein 1-like gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20160317 MGI PMID:24557841 1313740 Shcbp1l Shc SH2-domain binding protein 1-like gene MP:0001935 decreased litter size IAGP N RGD:5509061 20160317 MGI PMID:24557841 1313740 Shcbp1l Shc SH2-domain binding protein 1-like gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20160317 MGI PMID:24557841 1313740 Shcbp1l Shc SH2-domain binding protein 1-like gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20160317 MGI PMID:24557841 1313740 Shcbp1l Shc SH2-domain binding protein 1-like gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20160317 MGI PMID:24557841 1313740 Shcbp1l Shc SH2-domain binding protein 1-like gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20160317 MGI PMID:24557841 1313740 Shcbp1l Shc SH2-domain binding protein 1-like gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20160317 MGI PMID:24557841 1313742 Sh3tc1 SH3 domain and tetratricopeptide repeats 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1313742 Sh3tc1 SH3 domain and tetratricopeptide repeats 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20201022 MGI 1313742 Sh3tc1 SH3 domain and tetratricopeptide repeats 1 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1313742 Sh3tc1 SH3 domain and tetratricopeptide repeats 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20211021 MGI 1313742 Sh3tc1 SH3 domain and tetratricopeptide repeats 1 gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20210128 MGI 1313742 Sh3tc1 SH3 domain and tetratricopeptide repeats 1 gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20211021 MGI 1313742 Sh3tc1 SH3 domain and tetratricopeptide repeats 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1313742 Sh3tc1 SH3 domain and tetratricopeptide repeats 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1313742 Sh3tc1 SH3 domain and tetratricopeptide repeats 1 gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20210128 MGI 1313744 Smarce1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1313744 Smarce1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1313744 Smarce1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23198860 1313744 Smarce1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1313744 Smarce1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IEA N RGD:5509061 20241017 MGI 1313744 Smarce1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 gene MP:0014134 abnormal embryo morphology IEA N RGD:5509061 20240926 MGI 1313744 Smarce1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240926 MGI 1313746 Spns1 SPNS lysolipid transporter 1, lysophospholipid gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20160804 MGI 1313746 Spns1 SPNS lysolipid transporter 1, lysophospholipid gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1313753 Tbk1 TANK-binding kinase 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0001214 skin hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:18256672 1313753 Tbk1 TANK-binding kinase 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:23023393 1313753 Tbk1 TANK-binding kinase 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23023393 1313753 Tbk1 TANK-binding kinase 1 gene MP:0002451 abnormal macrophage physiology IEA N RGD:5509061 20141003 MGI 1313753 Tbk1 TANK-binding kinase 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23023393 1313753 Tbk1 TANK-binding kinase 1 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1313753 Tbk1 TANK-binding kinase 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1313753 Tbk1 TANK-binding kinase 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1313753 Tbk1 TANK-binding kinase 1 gene MP:0002607 decreased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1313753 Tbk1 TANK-binding kinase 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:10990461 1313753 Tbk1 TANK-binding kinase 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:10990461 1313753 Tbk1 TANK-binding kinase 1 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10990461 1313753 Tbk1 TANK-binding kinase 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1313753 Tbk1 TANK-binding kinase 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1313753 Tbk1 TANK-binding kinase 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:23023393 1313753 Tbk1 TANK-binding kinase 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0004971 dermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18256672 1313753 Tbk1 TANK-binding kinase 1 gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:18256672 1313753 Tbk1 TANK-binding kinase 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1313753 Tbk1 TANK-binding kinase 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:23023393 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18256672 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:18256672 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008555 abnormal interferon secretion IEA N RGD:5509061 20141003 MGI 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18256672 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313753 Tbk1 TANK-binding kinase 1 gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 1313753 Tbk1 TANK-binding kinase 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10990461 1313753 Tbk1 TANK-binding kinase 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15210742 1313753 Tbk1 TANK-binding kinase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20651301 1313755 Ndufab1 NADH:ubiquinone oxidoreductase subunit AB1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20201217 MGI PMID:31530015 1313755 Ndufab1 NADH:ubiquinone oxidoreductase subunit AB1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20201217 MGI PMID:31530015 1313755 Ndufab1 NADH:ubiquinone oxidoreductase subunit AB1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20201217 MGI PMID:31530015 1313755 Ndufab1 NADH:ubiquinone oxidoreductase subunit AB1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20201217 MGI PMID:31530015 1313755 Ndufab1 NADH:ubiquinone oxidoreductase subunit AB1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20201217 MGI PMID:31530015 1313755 Ndufab1 NADH:ubiquinone oxidoreductase subunit AB1 gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20201217 MGI PMID:31530015 1313755 Ndufab1 NADH:ubiquinone oxidoreductase subunit AB1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20201217 MGI PMID:31530015 1313755 Ndufab1 NADH:ubiquinone oxidoreductase subunit AB1 gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20201217 MGI PMID:31530015 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20210128 MGI 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20210617 MGI PMID:30814308 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20210617 MGI PMID:30814308 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20210617 MGI PMID:30814308 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20210617 MGI PMID:30814308 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20210617 MGI PMID:30814308 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0011017 increased body surface temperature IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20210422 MGI PMID:33177714 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20210617 MGI PMID:30814308 1313759 Usp20 ubiquitin specific peptidase 20 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20210617 MGI PMID:30814308 1313762 Mrps34 mitochondrial ribosomal protein S34 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20160512 MGI PMID:25816300 1313762 Mrps34 mitochondrial ribosomal protein S34 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160512 MGI PMID:25816300 1313762 Mrps34 mitochondrial ribosomal protein S34 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20160512 MGI PMID:25816300 1313762 Mrps34 mitochondrial ribosomal protein S34 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20160512 MGI PMID:25816300 1313762 Mrps34 mitochondrial ribosomal protein S34 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20160512 MGI PMID:25816300 1313762 Mrps34 mitochondrial ribosomal protein S34 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20160512 MGI PMID:25816300 1313762 Mrps34 mitochondrial ribosomal protein S34 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20160512 MGI PMID:25816300 1313762 Mrps34 mitochondrial ribosomal protein S34 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20160512 MGI PMID:25816300 1313762 Mrps34 mitochondrial ribosomal protein S34 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20160512 MGI PMID:25816300 1313762 Mrps34 mitochondrial ribosomal protein S34 gene MP:0014238 abnormal ribosome morphology IAGP N RGD:5509061 20230615 MGI PMID:25816300 1313764 Palmd palmdelphin gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1313764 Palmd palmdelphin gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1313764 Palmd palmdelphin gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20220310 MGI PMID:34636652 1313764 Palmd palmdelphin gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1313765 Tmem123 transmembrane protein 123 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1313767 Taf11 TATA-box binding protein associated factor 11 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313771 Ctdsp1 CTD small phosphatase 1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20220811 MGI 1313771 Ctdsp1 CTD small phosphatase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1313771 Ctdsp1 CTD small phosphatase 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20170105 MGI 1313771 Ctdsp1 CTD small phosphatase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20170105 MGI 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23479632 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:17356513 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:17304340 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:17304340 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:17304340 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17356513 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:17304340 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:17356513 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191003 MGI PMID:29168048 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17304340 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20191003 MGI PMID:29168048 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:16877435 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17003453 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20191003 MGI PMID:29168048 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0002064 seizures IAGP N RGD:5509061 20191003 MGI PMID:29168048 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17304340 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:17356513 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:17003453 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:16877435 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20191003 MGI PMID:29168048 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20191003 MGI PMID:29168048 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17254625 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:17304340 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:17356513 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20191003 MGI PMID:29168048 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16877435 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:17003453 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:17254625 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17003453 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0003927 increased cellular glucose import IAGP N RGD:5509061 20191003 MGI PMID:29168048 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17254625 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17356513 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17003453 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17254625 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:17254625 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20191003 MGI PMID:29168048 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17003453 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17356513 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:17356513 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17003453 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0005285 decreased unsaturated fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23479632 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20191003 MGI PMID:29168048 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17003453 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17003453 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:17003453 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17003453 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:17003453 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:17254625 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:17304340 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20191003 MGI PMID:29168048 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17356513 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16877435 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230601 MGI 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:17254625 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:16877435 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:17003453 1313773 Elovl4 ELOVL fatty acid elongase 4 gene MP:0030950 abnormal synaptic vesicle exocytosis IAGP N RGD:5509061 20191003 MGI PMID:29168048 1313774 Cox19 cytochrome c oxidase assembly protein 19 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1313774 Cox19 cytochrome c oxidase assembly protein 19 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20160421 MGI 1313774 Cox19 cytochrome c oxidase assembly protein 19 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1313774 Cox19 cytochrome c oxidase assembly protein 19 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313774 Cox19 cytochrome c oxidase assembly protein 19 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1313776 Ash2l ASH2 like histone lysine methyltransferase complex subunit gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20221215 MGI 1313776 Ash2l ASH2 like histone lysine methyltransferase complex subunit gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20463296 1313776 Ash2l ASH2 like histone lysine methyltransferase complex subunit gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20463296 1313776 Ash2l ASH2 like histone lysine methyltransferase complex subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313776 Ash2l ASH2 like histone lysine methyltransferase complex subunit gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20191128 MGI 1313776 Ash2l ASH2 like histone lysine methyltransferase complex subunit gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313778 Rrp1b ribosomal RNA processing 1B gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20191128 MGI 1313780 Ddx27 DEAD box helicase 27 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1313782 Il1f10 interleukin 1 family, member 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20191114 MGI PMID:29554104 1313792 Ormdl2 ORM1-like 2 (S. cerevisiae) gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20230202 MGI PMID:33643282 1313792 Ormdl2 ORM1-like 2 (S. cerevisiae) gene MP:0002531 abnormal type I hypersensitivity reaction IAGP N RGD:5509061 20230202 MGI PMID:33643282 1313792 Ormdl2 ORM1-like 2 (S. cerevisiae) gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20230202 MGI PMID:33643282 1313792 Ormdl2 ORM1-like 2 (S. cerevisiae) gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20230202 MGI PMID:33643282 1313792 Ormdl2 ORM1-like 2 (S. cerevisiae) gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20230202 MGI PMID:33643282 1313792 Ormdl2 ORM1-like 2 (S. cerevisiae) gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20230202 MGI PMID:33643282 1313792 Ormdl2 ORM1-like 2 (S. cerevisiae) gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240627 MGI PMID:37316542 1313792 Ormdl2 ORM1-like 2 (S. cerevisiae) gene MP:0020116 increased sphingosine level IAGP N RGD:5509061 20230202 MGI PMID:33643282 1313792 Ormdl2 ORM1-like 2 (S. cerevisiae) gene MP:0020582 increased ceramide level IAGP N RGD:5509061 20230202 MGI PMID:33643282 1313795 Ube2e2 ubiquitin-conjugating enzyme E2E 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1313796 Ecrg4 ECRG4 augurin precursor gene MP:0001257 increased body length IEA N RGD:5509061 20210128 MGI 1313796 Ecrg4 ECRG4 augurin precursor gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170323 MGI 1313796 Ecrg4 ECRG4 augurin precursor gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 1313796 Ecrg4 ECRG4 augurin precursor gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1313796 Ecrg4 ECRG4 augurin precursor gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1313796 Ecrg4 ECRG4 augurin precursor gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1313796 Ecrg4 ECRG4 augurin precursor gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20191003 MGI PMID:30745428 1313796 Ecrg4 ECRG4 augurin precursor gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20200402 MGI 1313796 Ecrg4 ECRG4 augurin precursor gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20211021 MGI 1313796 Ecrg4 ECRG4 augurin precursor gene MP:0012206 increased neuronal stem cell self-renewal IAGP N RGD:5509061 20191003 MGI PMID:30745428 1313796 Ecrg4 ECRG4 augurin precursor gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20191003 MGI PMID:30745428 1313796 Ecrg4 ECRG4 augurin precursor gene MP:0012361 decreased large unstained cell number IEA N RGD:5509061 20211021 MGI 1313798 Chit1 chitinase 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:22826322 1313801 Fbxo7 F-box protein 7 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1313801 Fbxo7 F-box protein 7 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0001577 anemia IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:21652635 1313801 Fbxo7 F-box protein 7 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21652635 1313801 Fbxo7 F-box protein 7 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20141003 MGI 1313801 Fbxo7 F-box protein 7 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20150430 MGI 1313801 Fbxo7 F-box protein 7 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1313801 Fbxo7 F-box protein 7 gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21652635 1313801 Fbxo7 F-box protein 7 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0008945 hyperchromic macrocytic anemia IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0010035 increased erythrocyte clearance IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1313801 Fbxo7 F-box protein 7 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:21652635 1313801 Fbxo7 F-box protein 7 gene MP:0011913 abnormal reticulocyte cell number IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0013762 abnormal effector T cell number IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313801 Fbxo7 F-box protein 7 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20190418 MGI PMID:30840666 1313802 Xkr8 X-linked Kx blood group related 8 gene MP:0001147 small testis IAGP N RGD:5509061 20240404 MGI PMID:31712393 1313802 Xkr8 X-linked Kx blood group related 8 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20240404 MGI PMID:31712393 1313802 Xkr8 X-linked Kx blood group related 8 gene MP:0001925 male infertility IAGP N RGD:5509061 20240404 MGI PMID:31712393 1313802 Xkr8 X-linked Kx blood group related 8 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20240404 MGI PMID:31712393 1313802 Xkr8 X-linked Kx blood group related 8 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20240404 MGI PMID:31712393 1313802 Xkr8 X-linked Kx blood group related 8 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20240404 MGI PMID:31712393 1313802 Xkr8 X-linked Kx blood group related 8 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240404 MGI PMID:31712393 1313802 Xkr8 X-linked Kx blood group related 8 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20240404 MGI PMID:31712393 1313802 Xkr8 X-linked Kx blood group related 8 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20240404 MGI PMID:31712393 1313802 Xkr8 X-linked Kx blood group related 8 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20240404 MGI PMID:31712393 1313802 Xkr8 X-linked Kx blood group related 8 gene MP:0006428 ectopic Sertoli cells IAGP N RGD:5509061 20240404 MGI PMID:31712393 1313802 Xkr8 X-linked Kx blood group related 8 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20240404 MGI PMID:31712393 1313802 Xkr8 X-linked Kx blood group related 8 gene MP:0009851 abnormal Sertoli cell phagocytosis IAGP N RGD:5509061 20240404 MGI PMID:31712393 1313802 Xkr8 X-linked Kx blood group related 8 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20240404 MGI PMID:31712393 1313804 Mgat4a mannoside acetylglucosaminyltransferase 4, isoenzyme A gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16377570 1313804 Mgat4a mannoside acetylglucosaminyltransferase 4, isoenzyme A gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16377570 1313804 Mgat4a mannoside acetylglucosaminyltransferase 4, isoenzyme A gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16377570 1313804 Mgat4a mannoside acetylglucosaminyltransferase 4, isoenzyme A gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:20015870 1313804 Mgat4a mannoside acetylglucosaminyltransferase 4, isoenzyme A gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16377570 1313804 Mgat4a mannoside acetylglucosaminyltransferase 4, isoenzyme A gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16377570 1313804 Mgat4a mannoside acetylglucosaminyltransferase 4, isoenzyme A gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16377570 1313804 Mgat4a mannoside acetylglucosaminyltransferase 4, isoenzyme A gene MP:0003926 decreased cellular glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:16377570 1313804 Mgat4a mannoside acetylglucosaminyltransferase 4, isoenzyme A gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16377570 1313804 Mgat4a mannoside acetylglucosaminyltransferase 4, isoenzyme A gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:16377570 1313804 Mgat4a mannoside acetylglucosaminyltransferase 4, isoenzyme A gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:16377570 1313804 Mgat4a mannoside acetylglucosaminyltransferase 4, isoenzyme A gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16377570 1313804 Mgat4a mannoside acetylglucosaminyltransferase 4, isoenzyme A gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16377570 1313805 Ccnq cyclin Q gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1313805 Ccnq cyclin Q gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1313805 Ccnq cyclin Q gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1313805 Ccnq cyclin Q gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313805 Ccnq cyclin Q gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313805 Ccnq cyclin Q gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1313807 Mkx mohawk homeobox gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:20498044 1313807 Mkx mohawk homeobox gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:20696843 1313807 Mkx mohawk homeobox gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:21254332 1313807 Mkx mohawk homeobox gene MP:0013179 wavy tail IAGP N RGD:5509061 20141003 MGI PMID:20696843 1313807 Mkx mohawk homeobox gene MP:0030799 abnormal tendon sheath morphology IAGP N RGD:5509061 20181011 MGI PMID:20696843 1313808 Pear1 platelet endothelial aggregation receptor 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20201022 MGI 1313808 Pear1 platelet endothelial aggregation receptor 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 1313808 Pear1 platelet endothelial aggregation receptor 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20170202 MGI PMID:27614188 1313811 Actl7b actin-like 7b gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1313811 Actl7b actin-like 7b gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1313811 Actl7b actin-like 7b gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 1313811 Actl7b actin-like 7b gene MP:0001147 small testis IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0001925 male infertility IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313811 Actl7b actin-like 7b gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20230622 MGI PMID:36617158 1313817 Taf1c TATA-box binding protein associated factor, RNA polymerase I, C gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1313817 Taf1c TATA-box binding protein associated factor, RNA polymerase I, C gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20241010 MGI 1313817 Taf1c TATA-box binding protein associated factor, RNA polymerase I, C gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241010 MGI 1313817 Taf1c TATA-box binding protein associated factor, RNA polymerase I, C gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241017 MGI 1313817 Taf1c TATA-box binding protein associated factor, RNA polymerase I, C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21349843 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0000371 diluted coat color IAGP N RGD:5509061 20181206 MGI PMID:29584722 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23673157 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23673157 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20181206 MGI PMID:29584722 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23673157 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23673157 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:21349843 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:21349843 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:23673157 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:23673157 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0003292 melena IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20181206 MGI PMID:29584722 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:21349843 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0004963 abnormal blastocoele morphology IAGP N RGD:5509061 20141003 MGI PMID:21349843 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20180531 MGI PMID:28533230 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20180531 MGI PMID:28533230 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:21349843 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23673157 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23673157 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20180531 MGI PMID:28533230 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0006064 abnormal superior vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23673157 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0008109 abnormal small intestinal microvillus morphology IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0008141 decreased small intestinal microvillus size IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20180531 MGI PMID:28533230 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20180531 MGI PMID:28533230 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20180531 MGI PMID:28533230 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0008727 increased heart right atrium size IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0008732 reduced hair shaft melanin granule number IAGP N RGD:5509061 20181227 MGI PMID:29584722 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23673157 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23673157 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0009979 abnormal cerebellum deep nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23673157 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0010493 abnormal atrium myocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23047693 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21349843 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21349843 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0011748 intestinal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0012028 abnormal visceral endoderm physiology IAGP N RGD:5509061 20141003 MGI PMID:23322734 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0014226 abnormal alveolar macrophage physiology IAGP N RGD:5509061 20180531 MGI PMID:28533230 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0014229 decreased alveolar macrophage number IAGP N RGD:5509061 20180531 MGI PMID:28533230 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0021086 decreased DNA replication IAGP N RGD:5509061 20220310 MGI PMID:21349843 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:23673157 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0030022 decreased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:23673157 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0030914 abnormal endosome to melanosome transport IAGP N RGD:5509061 20181227 MGI PMID:29584722 1313819 Pikfyve phosphoinositide kinase, FYVE type zinc finger containing gene MP:0030915 abnormal melanosome maturation IAGP N RGD:5509061 20181227 MGI PMID:29584722 1313823 Fbxw5 F-box and WD-40 domain protein 5 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20210114 MGI PMID:32971071 1313823 Fbxw5 F-box and WD-40 domain protein 5 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20210114 MGI PMID:32971071 1313823 Fbxw5 F-box and WD-40 domain protein 5 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20210114 MGI PMID:32971071 1313823 Fbxw5 F-box and WD-40 domain protein 5 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20210114 MGI PMID:32971071 1313823 Fbxw5 F-box and WD-40 domain protein 5 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20210114 MGI PMID:32971071 1313823 Fbxw5 F-box and WD-40 domain protein 5 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38697008 1313823 Fbxw5 F-box and WD-40 domain protein 5 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20210114 MGI PMID:32971071 1313823 Fbxw5 F-box and WD-40 domain protein 5 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20210114 MGI PMID:32971071 1313823 Fbxw5 F-box and WD-40 domain protein 5 gene MP:0031217 increased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20210114 MGI PMID:32971071 1313825 Zfp143 zinc finger protein 143 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:12904583 1313827 Rab40b Rab40B, member RAS oncogene family gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20231207 MGI 1313831 Unc45b unc-45 myosin chaperone B gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20111116 MGI 1313831 Unc45b unc-45 myosin chaperone B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313833 Vsx1 visual system homeobox 1 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20240523 MGI 1313833 Vsx1 visual system homeobox 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15043821 1313833 Vsx1 visual system homeobox 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:14745032 1313833 Vsx1 visual system homeobox 1 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23172916 1313833 Vsx1 visual system homeobox 1 gene MP:0006075 abnormal retina cone bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14745032 1313833 Vsx1 visual system homeobox 1 gene MP:0006075 abnormal retina cone bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15043821 1313835 Paip1 polyadenylate binding protein-interacting protein 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230119 MGI 1313835 Paip1 polyadenylate binding protein-interacting protein 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1313835 Paip1 polyadenylate binding protein-interacting protein 1 gene MP:0001925 male infertility IEA N RGD:5509061 20230119 MGI 1313835 Paip1 polyadenylate binding protein-interacting protein 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1313835 Paip1 polyadenylate binding protein-interacting protein 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230119 MGI 1313835 Paip1 polyadenylate binding protein-interacting protein 1 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20230119 MGI 1313835 Paip1 polyadenylate binding protein-interacting protein 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1313835 Paip1 polyadenylate binding protein-interacting protein 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230119 MGI 1313838 Lmo4 LIM domain only 4 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:19913004 1313838 Lmo4 LIM domain only 4 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:19913004 1313838 Lmo4 LIM domain only 4 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14966286 1313838 Lmo4 LIM domain only 4 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:14966285 1313838 Lmo4 LIM domain only 4 gene MP:0000861 disorganized barrel cortex IAGP N RGD:5509061 20141003 MGI PMID:16862160 1313838 Lmo4 LIM domain only 4 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:14966285 1313838 Lmo4 LIM domain only 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:14966285 1313838 Lmo4 LIM domain only 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:14966286 1313838 Lmo4 LIM domain only 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15691703 1313838 Lmo4 LIM domain only 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16949565 1313838 Lmo4 LIM domain only 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19913004 1313838 Lmo4 LIM domain only 4 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:15691703 1313838 Lmo4 LIM domain only 4 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:14966286 1313838 Lmo4 LIM domain only 4 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:14966286 1313838 Lmo4 LIM domain only 4 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:14966286 1313838 Lmo4 LIM domain only 4 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16949565 1313838 Lmo4 LIM domain only 4 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:16949565 1313838 Lmo4 LIM domain only 4 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:16949565 1313838 Lmo4 LIM domain only 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14966285 1313838 Lmo4 LIM domain only 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15691703 1313838 Lmo4 LIM domain only 4 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:14966285 1313838 Lmo4 LIM domain only 4 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:14966285 1313838 Lmo4 LIM domain only 4 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20171019 MGI PMID:14966285 1313838 Lmo4 LIM domain only 4 gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20200206 MGI PMID:31434684 1313838 Lmo4 LIM domain only 4 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20200206 MGI PMID:31434684 1313838 Lmo4 LIM domain only 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200206 MGI PMID:31434684 1313838 Lmo4 LIM domain only 4 gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20200206 MGI PMID:31434684 1313838 Lmo4 LIM domain only 4 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:16949565 1313838 Lmo4 LIM domain only 4 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:16949565 1313838 Lmo4 LIM domain only 4 gene MP:0003104 acrania IAGP N RGD:5509061 20141003 MGI PMID:19913004 1313838 Lmo4 LIM domain only 4 gene MP:0003104 acrania IAGP N RGD:5509061 20171019 MGI PMID:14966285 1313838 Lmo4 LIM domain only 4 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:19913004 1313838 Lmo4 LIM domain only 4 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:14966285 1313838 Lmo4 LIM domain only 4 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:19913004 1313838 Lmo4 LIM domain only 4 gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20141003 MGI PMID:19913004 1313838 Lmo4 LIM domain only 4 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20200206 MGI PMID:31434684 1313838 Lmo4 LIM domain only 4 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15691703 1313838 Lmo4 LIM domain only 4 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:19913004 1313838 Lmo4 LIM domain only 4 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:14966286 1313838 Lmo4 LIM domain only 4 gene MP:0004568 fusion of glossopharyngeal and vagus nerve IAGP N RGD:5509061 20141003 MGI PMID:14966286 1313838 Lmo4 LIM domain only 4 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:14966286 1313838 Lmo4 LIM domain only 4 gene MP:0004838 abnormal neural fold elevation formation IAGP N RGD:5509061 20141003 MGI PMID:15691703 1313838 Lmo4 LIM domain only 4 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:19913004 1313838 Lmo4 LIM domain only 4 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20200206 MGI PMID:31434684 1313838 Lmo4 LIM domain only 4 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:14966286 1313838 Lmo4 LIM domain only 4 gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20141003 MGI PMID:19913004 1313838 Lmo4 LIM domain only 4 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20618444 1313838 Lmo4 LIM domain only 4 gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20141003 MGI PMID:16949565 1313838 Lmo4 LIM domain only 4 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:20618444 1313838 Lmo4 LIM domain only 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14966286 1313838 Lmo4 LIM domain only 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14966285 1313838 Lmo4 LIM domain only 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19913004 1313838 Lmo4 LIM domain only 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14966285 1313838 Lmo4 LIM domain only 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15691703 1313838 Lmo4 LIM domain only 4 gene MP:0012686 everted embryonic neuroepithelium IAGP N RGD:5509061 20141003 MGI PMID:15691703 1313838 Lmo4 LIM domain only 4 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15691703 1313838 Lmo4 LIM domain only 4 gene MP:0012704 abnormal embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15691703 1313839 Dip2b disco interacting protein 2 homolog B gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20160804 MGI 1313839 Dip2b disco interacting protein 2 homolog B gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20160804 MGI 1313841 Spock3 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20210819 MGI PMID:25138526 1313841 Spock3 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20210819 MGI PMID:25138526 1313841 Spock3 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20210819 MGI PMID:25138526 1313841 Spock3 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20210819 MGI PMID:25138526 1313841 Spock3 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23418755 1313841 Spock3 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20210819 MGI PMID:25138526 1313841 Spock3 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3 gene MP:0005603 neuron hypertrophy IAGP N RGD:5509061 20210819 MGI PMID:25138526 1313841 Spock3 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3 gene MP:0008946 abnormal neuron number IAGP N RGD:5509061 20210819 MGI PMID:25138526 1313841 Spock3 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3 gene MP:0020067 increased neocortex size IAGP N RGD:5509061 20210819 MGI PMID:25138526 1313841 Spock3 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20210819 MGI PMID:25138526 1313842 Prdm11 PR domain containing 11 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20191226 MGI PMID:26263558 1313842 Prdm11 PR domain containing 11 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20191226 MGI PMID:26263558 1313842 Prdm11 PR domain containing 11 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20191226 MGI PMID:25499759 1313842 Prdm11 PR domain containing 11 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20191226 MGI PMID:26263558 1313842 Prdm11 PR domain containing 11 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20191226 MGI PMID:25499759 1313842 Prdm11 PR domain containing 11 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20191226 MGI PMID:26263558 1313842 Prdm11 PR domain containing 11 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20191226 MGI PMID:26263558 1313842 Prdm11 PR domain containing 11 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20191226 MGI PMID:26263558 1313842 Prdm11 PR domain containing 11 gene MP:0013707 abnormal hematopoietic precursor cell morphology IAGP N RGD:5509061 20191226 MGI PMID:23978475 1313842 Prdm11 PR domain containing 11 gene MP:0020464 decreased megakaryocyte progenitor cell number IAGP N RGD:5509061 20191226 MGI PMID:23978475 1313842 Prdm11 PR domain containing 11 gene MP:0020466 increased megakaryocyte progenitor cell proliferation IAGP N RGD:5509061 20191226 MGI PMID:23978475 1313846 Tmem126a transmembrane protein 126A gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1313846 Tmem126a transmembrane protein 126A gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1313846 Tmem126a transmembrane protein 126A gene MP:0013764 decreased T-helper cell number IEA N RGD:5509061 20201231 MGI 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20200514 MGI 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20201022 MGI PMID:30571485 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0001786 skin edema IAGP N RGD:5509061 20201022 MGI PMID:30571485 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20201022 MGI PMID:30571485 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0001914 hemorrhage IAGP N RGD:5509061 20201022 MGI PMID:30571485 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20201022 MGI PMID:30571485 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20210114 MGI PMID:32152231 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20201022 MGI PMID:30571485 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20201022 MGI PMID:30571485 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20201022 MGI PMID:30571485 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20201022 MGI PMID:30571485 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20201022 MGI PMID:30571485 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20210114 MGI PMID:32152231 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0013258 abnormal extracellular matrix morphology IAGP N RGD:5509061 20201022 MGI PMID:30571485 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0014264 abnormal perivascular vein cell coverage IAGP N RGD:5509061 20230706 MGI PMID:30571485 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0020326 dilated capillary IAGP N RGD:5509061 20201022 MGI PMID:30571485 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0020327 abnormal capillary branching pattern IAGP N RGD:5509061 20201022 MGI PMID:30571485 1313850 Adtrp androgen dependent TFPI regulating protein gene MP:0020331 increased capillary tortuosity IAGP N RGD:5509061 20201022 MGI PMID:30571485 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20240523 MGI 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0001625 cardiac hypertrophy IEA N RGD:5509061 20141003 MGI 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20141003 MGI 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0001925 male infertility IEA N RGD:5509061 20230119 MGI 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20240523 MGI 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20141003 MGI 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20240523 MGI 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20240523 MGI 1313852 Bicral BRD4 interacting chromatin remodeling complex associated protein like gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IEA N RGD:5509061 20141003 MGI 1313856 Cmtm7 CKLF-like MARVEL transmembrane domain containing 7 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20171228 MGI PMID:24080084 1313856 Cmtm7 CKLF-like MARVEL transmembrane domain containing 7 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20171228 MGI PMID:24080084 1313856 Cmtm7 CKLF-like MARVEL transmembrane domain containing 7 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1313856 Cmtm7 CKLF-like MARVEL transmembrane domain containing 7 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20171228 MGI PMID:24080084 1313856 Cmtm7 CKLF-like MARVEL transmembrane domain containing 7 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20171228 MGI PMID:24080084 1313856 Cmtm7 CKLF-like MARVEL transmembrane domain containing 7 gene MP:0008164 abnormal B-1a B cell morphology IAGP N RGD:5509061 20171228 MGI PMID:24080084 1313856 Cmtm7 CKLF-like MARVEL transmembrane domain containing 7 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20171228 MGI PMID:24080084 1313856 Cmtm7 CKLF-like MARVEL transmembrane domain containing 7 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20171228 MGI PMID:24080084 1313856 Cmtm7 CKLF-like MARVEL transmembrane domain containing 7 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20171228 MGI PMID:24080084 1313860 Naa25 N(alpha)-acetyltransferase 25, NatB auxiliary subunit gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210826 MGI 1313860 Naa25 N(alpha)-acetyltransferase 25, NatB auxiliary subunit gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1313860 Naa25 N(alpha)-acetyltransferase 25, NatB auxiliary subunit gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220519 MGI 1313860 Naa25 N(alpha)-acetyltransferase 25, NatB auxiliary subunit gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220519 MGI 1313860 Naa25 N(alpha)-acetyltransferase 25, NatB auxiliary subunit gene MP:0001399 hyperactivity IEA N RGD:5509061 20221215 MGI 1313860 Naa25 N(alpha)-acetyltransferase 25, NatB auxiliary subunit gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1313860 Naa25 N(alpha)-acetyltransferase 25, NatB auxiliary subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1313860 Naa25 N(alpha)-acetyltransferase 25, NatB auxiliary subunit gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313860 Naa25 N(alpha)-acetyltransferase 25, NatB auxiliary subunit gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1313862 Rnasek ribonuclease, RNase K gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1313862 Rnasek ribonuclease, RNase K gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20170105 MGI 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220519 MGI 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20221215 MGI 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0002981 increased liver weight IEA N RGD:5509061 20220519 MGI 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20170105 MGI 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20221215 MGI 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0011402 renal cast IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0011483 renal glomerular synechia IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313864 Rhpn1 rhophilin, Rho GTPase binding protein 1 gene MP:0011868 podocyte microvillus transformation IAGP N RGD:5509061 20191003 MGI PMID:25071083 1313866 Tmem254 transmembrane protein 254 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20231207 MGI 1313867 Slc25a42 solute carrier family 25, member 42 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1313867 Slc25a42 solute carrier family 25, member 42 gene MP:0001925 male infertility IEA N RGD:5509061 20220811 MGI 1313867 Slc25a42 solute carrier family 25, member 42 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1313867 Slc25a42 solute carrier family 25, member 42 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1313868 Il34 interleukin 34 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22729249 1313868 Il34 interleukin 34 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22729249 1313868 Il34 interleukin 34 gene MP:0005398 decreased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:22729249 1313868 Il34 interleukin 34 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:22729249 1313868 Il34 interleukin 34 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22729249 1313868 Il34 interleukin 34 gene MP:0008118 absent Langerhans cell IAGP N RGD:5509061 20141003 MGI PMID:22729249 1313868 Il34 interleukin 34 gene MP:0008119 decreased Langerhans cell number IAGP N RGD:5509061 20141003 MGI PMID:22729249 1313868 Il34 interleukin 34 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22729249 1313868 Il34 interleukin 34 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22729249 1313868 Il34 interleukin 34 gene MP:0020943 increased susceptibility to Flaviviridae infection IAGP N RGD:5509061 20200430 MGI PMID:22729249 1313868 Il34 interleukin 34 gene MP:0031044 increased susceptibility to Flaviviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:22729249 1313869 Sarnp SAP domain containing ribonucleoprotein gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1313869 Sarnp SAP domain containing ribonucleoprotein gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 1313869 Sarnp SAP domain containing ribonucleoprotein gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1313869 Sarnp SAP domain containing ribonucleoprotein gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1313869 Sarnp SAP domain containing ribonucleoprotein gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1313869 Sarnp SAP domain containing ribonucleoprotein gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1313869 Sarnp SAP domain containing ribonucleoprotein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1313869 Sarnp SAP domain containing ribonucleoprotein gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 1313871 Abhd8 abhydrolase domain containing 8 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210128 MGI 1313871 Abhd8 abhydrolase domain containing 8 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1313871 Abhd8 abhydrolase domain containing 8 gene MP:0001399 hyperactivity IEA N RGD:5509061 20170105 MGI 1313871 Abhd8 abhydrolase domain containing 8 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 1313871 Abhd8 abhydrolase domain containing 8 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1313871 Abhd8 abhydrolase domain containing 8 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 1313871 Abhd8 abhydrolase domain containing 8 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1313875 Lsm14a LSM14A mRNA processing body assembly factor gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1313875 Lsm14a LSM14A mRNA processing body assembly factor gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1313875 Lsm14a LSM14A mRNA processing body assembly factor gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1313875 Lsm14a LSM14A mRNA processing body assembly factor gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1313875 Lsm14a LSM14A mRNA processing body assembly factor gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1313877 Hsh2d hematopoietic SH2 domain containing gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16880512 1313877 Hsh2d hematopoietic SH2 domain containing gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16880512 1313877 Hsh2d hematopoietic SH2 domain containing gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16880512 1313877 Hsh2d hematopoietic SH2 domain containing gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16880512 1313877 Hsh2d hematopoietic SH2 domain containing gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:16880512 1313880 Taf1a TATA-box binding protein associated factor, RNA polymerase I, A gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241010 MGI 1313880 Taf1a TATA-box binding protein associated factor, RNA polymerase I, A gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241017 MGI 1313880 Taf1a TATA-box binding protein associated factor, RNA polymerase I, A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1313880 Taf1a TATA-box binding protein associated factor, RNA polymerase I, A gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20241010 MGI 1313882 P3h3 prolyl 3-hydroxylase 3 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1313882 P3h3 prolyl 3-hydroxylase 3 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1313882 P3h3 prolyl 3-hydroxylase 3 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20170810 MGI PMID:28115524 1313882 P3h3 prolyl 3-hydroxylase 3 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20170810 MGI PMID:28115524 1313884 Catsper3 cation channel, sperm associated 3 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210520 MGI 1313884 Catsper3 cation channel, sperm associated 3 gene MP:0000642 enlarged adrenal glands IEA N RGD:5509061 20210520 MGI 1313884 Catsper3 cation channel, sperm associated 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17227845 1313884 Catsper3 cation channel, sperm associated 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17344468 1313884 Catsper3 cation channel, sperm associated 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1313884 Catsper3 cation channel, sperm associated 3 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:17227845 1313884 Catsper3 cation channel, sperm associated 3 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:17344468 1313884 Catsper3 cation channel, sperm associated 3 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17227845 1313884 Catsper3 cation channel, sperm associated 3 gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20141003 MGI PMID:17227845 1313884 Catsper3 cation channel, sperm associated 3 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:17227845 1313884 Catsper3 cation channel, sperm associated 3 gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 1313884 Catsper3 cation channel, sperm associated 3 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17227845 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12130785 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12130785 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:14614141 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0005230 ectrodactyly IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12130785 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12417741 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:12130785 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:14614141 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21765423 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:14614141 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12417741 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0010395 abnormal pharyngeal arch development IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0011998 decreased embryonic cilium length IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0012531 delayed limb development IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0012720 elongated neck IAGP N RGD:5509061 20141003 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:19000668 1313886 Mbd4 methyl-CpG binding domain protein 4 gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:19000668 1313888 Tbx5 T-box 5 gene MP:0000158 absent sternum IAGP N RGD:5509061 20141003 MGI PMID:12736217 1313888 Tbx5 T-box 5 gene MP:0000158 absent sternum IAGP N RGD:5509061 20150903 MGI PMID:25468972 1313888 Tbx5 T-box 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16380715 1313888 Tbx5 T-box 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16380715 1313888 Tbx5 T-box 5 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:16380715 1313888 Tbx5 T-box 5 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:20152185 1313888 Tbx5 T-box 5 gene MP:0000551 absent forelimb IAGP N RGD:5509061 20141003 MGI PMID:12736217 1313888 Tbx5 T-box 5 gene MP:0000551 absent forelimb IAGP N RGD:5509061 20150903 MGI PMID:25468972 1313888 Tbx5 T-box 5 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:22728936 1313888 Tbx5 T-box 5 gene MP:0001657 abnormal induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22728936 1313888 Tbx5 T-box 5 gene MP:0001677 absent apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:12736217 1313888 Tbx5 T-box 5 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12736217 1313888 Tbx5 T-box 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22728936 1313888 Tbx5 T-box 5 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:16380715 1313888 Tbx5 T-box 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16380715 1313888 Tbx5 T-box 5 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:15289437 1313888 Tbx5 T-box 5 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:22728936 1313888 Tbx5 T-box 5 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20150903 MGI PMID:25468972 1313888 Tbx5 T-box 5 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0004055 heart atrium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0004116 abnormal atrioventricular bundle conduction IAGP N RGD:5509061 20141003 MGI PMID:22728936 1313888 Tbx5 T-box 5 gene MP:0004117 abnormal atrioventricular bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15289437 1313888 Tbx5 T-box 5 gene MP:0004122 abnormal sinus arrhythmia IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0004123 abnormal impulse conducting system morphology IAGP N RGD:5509061 20141003 MGI PMID:15289437 1313888 Tbx5 T-box 5 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0004339 absent clavicle IAGP N RGD:5509061 20141003 MGI PMID:12736217 1313888 Tbx5 T-box 5 gene MP:0004341 absent scapula IAGP N RGD:5509061 20141003 MGI PMID:12736217 1313888 Tbx5 T-box 5 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:12736217 1313888 Tbx5 T-box 5 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20150903 MGI PMID:25468972 1313888 Tbx5 T-box 5 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:20152185 1313888 Tbx5 T-box 5 gene MP:0006141 abnormal atrioventricular node conduction IAGP N RGD:5509061 20141003 MGI PMID:15289437 1313888 Tbx5 T-box 5 gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:20152185 1313888 Tbx5 T-box 5 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:22728936 1313888 Tbx5 T-box 5 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20141003 MGI PMID:22728936 1313888 Tbx5 T-box 5 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:15289437 1313888 Tbx5 T-box 5 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:16380715 1313888 Tbx5 T-box 5 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16380715 1313888 Tbx5 T-box 5 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16380715 1313888 Tbx5 T-box 5 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:22728936 1313888 Tbx5 T-box 5 gene MP:0010520 sinoatrial block IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0010566 abnormal left posterior bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15289437 1313888 Tbx5 T-box 5 gene MP:0010567 abnormal right bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15289437 1313888 Tbx5 T-box 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11572777 1313888 Tbx5 T-box 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16380715 1313888 Tbx5 T-box 5 gene MP:0011953 prolonged PQ interval IAGP N RGD:5509061 20141003 MGI PMID:15289437 1313888 Tbx5 T-box 5 gene MP:0011953 prolonged PQ interval IAGP N RGD:5509061 20141003 MGI PMID:16870172 1313888 Tbx5 T-box 5 gene MP:0013164 abnormal forelimb bud morphology IAGP N RGD:5509061 20150528 MGI PMID:12736217 1313888 Tbx5 T-box 5 gene MP:0013165 absent forelimb buds IAGP N RGD:5509061 20150528 MGI PMID:12736217 1313888 Tbx5 T-box 5 gene MP:0031530 abnormal heart ventricle shape IAGP N RGD:5509061 20240104 MGI PMID:11572777 1313891 Larp4 La ribonucleoprotein 4 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20230831 MGI PMID:28895529 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19615442 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:11731460 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:19615442 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:11532921 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11820816 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000445 short snout IAGP N RGD:5509061 20171012 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:16845372 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:16845372 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:19615442 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20150122 MGI PMID:24457099 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20816794 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23364326 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20141003 MGI PMID:15917450 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:23364326 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:17980036 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:11820816 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:9521907 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11820816 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16845372 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:17980036 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9521907 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000906 abnormal trigeminal V mesencephalic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000906 abnormal trigeminal V mesencephalic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:11532921 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:11820816 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:15201224 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:17980036 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:20816794 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11532921 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11731460 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11820816 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19615442 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11532921 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11820816 1313893 Otx2 orthodenticle homeobox 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001061 abnormal oculomotor nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001061 abnormal oculomotor nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001063 abnormal trochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001063 abnormal trochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11731460 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16845372 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:16845372 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001329 retina hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:19615442 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001684 abnormal axial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16845372 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:11532921 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:11820816 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:11532921 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23811236 1313893 Otx2 orthodenticle homeobox 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23811236 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:11532921 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16845372 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9521907 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11820816 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12915318 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19615442 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:11291865 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002243 abnormal vomeronasal organ morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002698 abnormal sclera morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:23811236 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12764108 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003006 abnormal hippocampal fornix morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:11532921 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:11731460 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:15201223 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:16845372 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:19615442 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:20667915 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:9811592 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12764108 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:16845372 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:23364326 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:17980036 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:11820816 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:11532921 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:11731460 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:19615442 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:9811592 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003877 abnormal serotonergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12764108 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:9811592 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004096 abnormal midbrain-hindbrain boundary development IAGP N RGD:5509061 20141003 MGI PMID:11731460 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004162 abnormal mammillary body morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9811592 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20150122 MGI PMID:24457099 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20816794 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004280 abnormal oculomotor nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004450 presphenoid bone hypoplasia IAGP N RGD:5509061 20171207 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004457 abnormal orbitosphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004539 absent maxilla IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23811236 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20171012 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:12652306 1313893 Otx2 orthodenticle homeobox 2 gene MP:0004990 abnormal ciliary ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10985852 1313893 Otx2 orthodenticle homeobox 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:11291865 1313893 Otx2 orthodenticle homeobox 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16256739 1313893 Otx2 orthodenticle homeobox 2 gene MP:0005247 abnormal extraocular muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0005261 aniridia IAGP N RGD:5509061 20160310 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0005315 absent pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0005549 retina pigment epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006100 abnormal tegmentum morphology IAGP N RGD:5509061 20141003 MGI PMID:12652306 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006100 abnormal tegmentum morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006101 absent tegmentum IAGP N RGD:5509061 20141003 MGI PMID:20816794 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006105 small tectum IAGP N RGD:5509061 20141003 MGI PMID:12652306 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006106 absent tectum IAGP N RGD:5509061 20141003 MGI PMID:20816794 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:9449667 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006293 absent nasal placodes IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006293 absent nasal placodes IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006294 absent optic vesicle IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006294 absent optic vesicle IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11532921 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11731460 1313893 Otx2 orthodenticle homeobox 2 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9811592 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008262 abnormal hippocampus region morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008325 abnormal gonadotroph morphology IAGP N RGD:5509061 20141003 MGI PMID:23811236 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008335 decreased gonadotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:23811236 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008384 absent nasal capsule IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008914 enlarged cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008914 enlarged cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:23364326 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20161103 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20161103 MGI PMID:15917450 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:16845372 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009048 enlarged tectum IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009324 absent hippocampal fimbria IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009578 otocephaly IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009579 acephaly IAGP N RGD:5509061 20141003 MGI PMID:10985852 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009579 acephaly IAGP N RGD:5509061 20141003 MGI PMID:11532921 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009579 acephaly IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009579 acephaly IAGP N RGD:5509061 20141003 MGI PMID:11731460 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009579 acephaly IAGP N RGD:5509061 20141003 MGI PMID:19615442 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009579 acephaly IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009579 acephaly IAGP N RGD:5509061 20141003 MGI PMID:9811592 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009579 acephaly IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009637 abnormal pretectal region morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009637 abnormal pretectal region morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009905 absent tongue IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21057506 1313893 Otx2 orthodenticle homeobox 2 gene MP:0009951 abnormal olfactory bulb mitral cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0010893 abnormal posterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0010893 abnormal posterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:11532921 1313893 Otx2 orthodenticle homeobox 2 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:11731460 1313893 Otx2 orthodenticle homeobox 2 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:9811592 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11820816 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17980036 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12652306 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9521907 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11820816 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23811236 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20141003 MGI PMID:9811592 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:21057506 1313893 Otx2 orthodenticle homeobox 2 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012083 absent foregut IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:15201223 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:15201224 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:20816794 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:9449667 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:11532921 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012090 midbrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:24234651 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:11820816 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:12652306 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:20816794 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:16845372 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:15201223 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:9449667 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:11532921 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:7588062 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:9811592 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012170 absent optic placodes IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012176 abnormal head development IAGP N RGD:5509061 20141003 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012247 absent cornea IAGP N RGD:5509061 20160310 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012267 abnormal red nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012276 absent prechordal mesoderm IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012516 absent metencephalon IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012516 absent metencephalon IAGP N RGD:5509061 20141003 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012517 absent diencephalon IAGP N RGD:5509061 20141003 MGI PMID:11820816 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012517 absent diencephalon IAGP N RGD:5509061 20141003 MGI PMID:15201223 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012517 absent diencephalon IAGP N RGD:5509061 20141003 MGI PMID:15201224 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012517 absent diencephalon IAGP N RGD:5509061 20141003 MGI PMID:20667915 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012517 absent diencephalon IAGP N RGD:5509061 20141003 MGI PMID:20816794 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012525 abnormal rhombic lip morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:11291865 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0012786 increased rhombomere 1 size IAGP N RGD:5509061 20141003 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0013595 absent vomeronasal organ IAGP N RGD:5509061 20150319 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0013906 absent embryonic telencephalon IAGP N RGD:5509061 20150924 MGI PMID:11731459 1313893 Otx2 orthodenticle homeobox 2 gene MP:0013906 absent embryonic telencephalon IAGP N RGD:5509061 20150924 MGI PMID:11820816 1313893 Otx2 orthodenticle homeobox 2 gene MP:0014061 ethmocephaly IAGP N RGD:5509061 20230810 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0020515 abnormal visceral yolk sac endoderm morphology IAGP N RGD:5509061 20180125 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0020516 abnormal visceral yolk sac mesenchyme morphology IAGP N RGD:5509061 20180125 MGI PMID:8565836 1313893 Otx2 orthodenticle homeobox 2 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0020534 increased pons size IAGP N RGD:5509061 20180301 MGI PMID:20816794 1313893 Otx2 orthodenticle homeobox 2 gene MP:0020534 increased pons size IAGP N RGD:5509061 20180301 MGI PMID:9895322 1313893 Otx2 orthodenticle homeobox 2 gene MP:0020543 decreased substantia nigra size IAGP N RGD:5509061 20180301 MGI PMID:9077465 1313893 Otx2 orthodenticle homeobox 2 gene MP:0030102 absent orbitosphenoid bone IAGP N RGD:5509061 20170928 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0030320 abnormal temporal bone tympanic part morphology IAGP N RGD:5509061 20171109 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0030324 abnormal anterior head development IAGP N RGD:5509061 20171109 MGI PMID:9811592 1313893 Otx2 orthodenticle homeobox 2 gene MP:0030324 abnormal anterior head development IAGP N RGD:5509061 20180118 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0030558 absent nasopharynx IAGP N RGD:5509061 20191219 MGI PMID:7590242 1313893 Otx2 orthodenticle homeobox 2 gene MP:0031442 enlarged cerebral aqueduct IAGP N RGD:5509061 20221103 MGI PMID:9077465 1313895 H1f1 H1.1 linker histone, cluster member gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:15685642 1313895 H1f1 H1.1 linker histone, cluster member gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15685642 1313895 H1f1 H1.1 linker histone, cluster member gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15685642 1313895 H1f1 H1.1 linker histone, cluster member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10666340 1313895 H1f1 H1.1 linker histone, cluster member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12930723 1313895 H1f1 H1.1 linker histone, cluster member gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15685642 1313895 H1f1 H1.1 linker histone, cluster member gene MP:0003718 maternal effect IAGP N RGD:5509061 20231207 MGI PMID:37062716 1313895 H1f1 H1.1 linker histone, cluster member gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:15685642 1313895 H1f1 H1.1 linker histone, cluster member gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191017 MGI PMID:15685642 1313895 H1f1 H1.1 linker histone, cluster member gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20200227 MGI PMID:15685642 1313897 Caprin1 cell cycle associated protein 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:20861386 1313897 Caprin1 cell cycle associated protein 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:20861386 1313897 Caprin1 cell cycle associated protein 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:20861386 1313897 Caprin1 cell cycle associated protein 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20861386 1313897 Caprin1 cell cycle associated protein 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:20861386 1313897 Caprin1 cell cycle associated protein 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20861386 1313897 Caprin1 cell cycle associated protein 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:20861386 1313897 Caprin1 cell cycle associated protein 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:20861386 1313897 Caprin1 cell cycle associated protein 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20861386 1313897 Caprin1 cell cycle associated protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20861386 1313899 D7Ertd443e DNA segment, Chr 7, ERATO Doi 443, expressed gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1313899 D7Ertd443e DNA segment, Chr 7, ERATO Doi 443, expressed gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1313899 D7Ertd443e DNA segment, Chr 7, ERATO Doi 443, expressed gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1313901 Armh3 armadillo-like helical domain containing 3 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1313901 Armh3 armadillo-like helical domain containing 3 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1313901 Armh3 armadillo-like helical domain containing 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20160114 MGI 1313901 Armh3 armadillo-like helical domain containing 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1313903 Ap1g2 adaptor protein complex AP-1, gamma 2 subunit gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1313903 Ap1g2 adaptor protein complex AP-1, gamma 2 subunit gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 1313905 Foxn3 forkhead box N3 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0000120 malocclusion IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0000161 scoliosis IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0000433 microcephaly IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1313905 Foxn3 forkhead box N3 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0009891 abnormal palate bone morphology IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313905 Foxn3 forkhead box N3 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0030082 long lower incisors IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0030083 long upper incisors IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0030279 thin neurocranium IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313905 Foxn3 forkhead box N3 gene MP:0030320 abnormal temporal bone tympanic part morphology IAGP N RGD:5509061 20180315 MGI PMID:20691664 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20201022 MGI 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20181227 MGI 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20181227 MGI 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20210128 MGI 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20170105 MGI 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20210128 MGI 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1313911 Zswim1 zinc finger SWIM-type containing 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1313913 Hat1 histone aminotransferase 1 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0003786 premature aging IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0005649 increased spleen neoplasm incidence IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0010294 increased kidney tumor incidence IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:23754951 1313913 Hat1 histone aminotransferase 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313913 Hat1 histone aminotransferase 1 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20220929 MGI PMID:31290578 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0001147 small testis IAGP N RGD:5509061 20180222 MGI PMID:29247201 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0001147 small testis IAGP N RGD:5509061 20181220 MGI PMID:29848638 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0001147 small testis IAGP N RGD:5509061 20220721 MGI PMID:29866902 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20181220 MGI PMID:29848638 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20180222 MGI PMID:29247201 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20190502 MGI 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0001925 male infertility IAGP N RGD:5509061 20180222 MGI PMID:29247201 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0001925 male infertility IAGP N RGD:5509061 20181220 MGI PMID:29848638 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0001925 male infertility IAGP N RGD:5509061 20220721 MGI PMID:29866902 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20220721 MGI PMID:29866902 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20211021 MGI 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220721 MGI PMID:29866902 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0004930 small epididymis IAGP N RGD:5509061 20181220 MGI PMID:29848638 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0005159 azoospermia IAGP N RGD:5509061 20180222 MGI PMID:29247201 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220721 MGI PMID:29866902 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220721 MGI PMID:29866902 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20180222 MGI PMID:29247201 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220721 MGI PMID:29866902 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20180222 MGI PMID:29247201 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20220721 MGI PMID:29866902 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20181220 MGI PMID:29848638 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220721 MGI PMID:29866902 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:29247201 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220721 MGI PMID:29866902 1313914 Sox30 SRY (sex determining region Y)-box 30 gene MP:0031355 abnormal proacrosomal vesicle fusion IAGP N RGD:5509061 20220721 MGI PMID:29866902 1313916 Nat8l N-acetyltransferase 8-like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160609 MGI PMID:26511242 1313916 Nat8l N-acetyltransferase 8-like gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:22940080 1313916 Nat8l N-acetyltransferase 8-like gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22940080 1313916 Nat8l N-acetyltransferase 8-like gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160609 MGI PMID:26511242 1313916 Nat8l N-acetyltransferase 8-like gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:22940080 1313916 Nat8l N-acetyltransferase 8-like gene MP:0002083 premature death IAGP N RGD:5509061 20160609 MGI PMID:26511242 1313916 Nat8l N-acetyltransferase 8-like gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20160609 MGI PMID:26511242 1313916 Nat8l N-acetyltransferase 8-like gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20160609 MGI PMID:26511242 1313916 Nat8l N-acetyltransferase 8-like gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:22940080 1313916 Nat8l N-acetyltransferase 8-like gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20160609 MGI PMID:26511242 1313916 Nat8l N-acetyltransferase 8-like gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20160609 MGI PMID:26511242 1313916 Nat8l N-acetyltransferase 8-like gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:22940080 1313916 Nat8l N-acetyltransferase 8-like gene MP:0003354 astrocytosis IAGP N RGD:5509061 20160609 MGI PMID:26511242 1313916 Nat8l N-acetyltransferase 8-like gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20160609 MGI PMID:26511242 1313916 Nat8l N-acetyltransferase 8-like gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20160609 MGI PMID:26511242 1313916 Nat8l N-acetyltransferase 8-like gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20160609 MGI PMID:26511242 1313916 Nat8l N-acetyltransferase 8-like gene MP:0011621 abnormal habituation to a novel object IAGP N RGD:5509061 20141003 MGI PMID:22940080 1313916 Nat8l N-acetyltransferase 8-like gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:33638175 1313921 Tmem14c transmembrane protein 14C gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:25157825 1313921 Tmem14c transmembrane protein 14C gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:25157825 1313921 Tmem14c transmembrane protein 14C gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:25157825 1313921 Tmem14c transmembrane protein 14C gene MP:0001588 abnormal hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:25157825 1313921 Tmem14c transmembrane protein 14C gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:25157825 1313921 Tmem14c transmembrane protein 14C gene MP:0008956 decreased cellular hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:25157825 1313921 Tmem14c transmembrane protein 14C gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:25157825 1313921 Tmem14c transmembrane protein 14C gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:25157825 1313924 Fbxl4 F-box and leucine-rich repeat protein 4 gene MP:0000160 kyphosis IAGP N RGD:5509061 20210415 MGI PMID:32525278 1313924 Fbxl4 F-box and leucine-rich repeat protein 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210415 MGI PMID:32525278 1313924 Fbxl4 F-box and leucine-rich repeat protein 4 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20210415 MGI PMID:32525278 1313924 Fbxl4 F-box and leucine-rich repeat protein 4 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20210415 MGI PMID:32525278 1313924 Fbxl4 F-box and leucine-rich repeat protein 4 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20210415 MGI PMID:32525278 1313924 Fbxl4 F-box and leucine-rich repeat protein 4 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20210415 MGI PMID:32525278 1313924 Fbxl4 F-box and leucine-rich repeat protein 4 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210415 MGI PMID:32525278 1313924 Fbxl4 F-box and leucine-rich repeat protein 4 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20210415 MGI PMID:32525278 1313924 Fbxl4 F-box and leucine-rich repeat protein 4 gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20210415 MGI PMID:32525278 1313931 Mknk2 MAP kinase-interacting serine/threonine kinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15254222 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:17174920 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17330141 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000791 delaminated cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17330141 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:17174920 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12695510 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16102539 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16102539 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16102539 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12695510 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16102539 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12695510 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:17174920 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:12695510 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17174920 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:17330141 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12695510 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:12695510 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:12695510 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:12695510 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20180301 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:12695510 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:12695510 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10380922 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16481437 1313933 Lrp8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor gene MP:0030956 abnormal neuronal precursor cell migration IAGP N RGD:5509061 20190725 MGI PMID:17494763 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:15798193 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15798193 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15798193 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15798193 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20240118 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16317048 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:15798193 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0010496 abnormal pectinate muscle morphology IAGP N RGD:5509061 20240118 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15976450 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15798193 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0011198 absent proamniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:15798193 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0020135 abnormal heart ventricle wall thickness IAGP N RGD:5509061 20240118 MGI PMID:19652092 1313938 Lims1 LIM and senescent cell antigen-like domains 1 gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:19652092 1313939 Bmerb1 bMERB domain containing 1 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20200402 MGI 1313939 Bmerb1 bMERB domain containing 1 gene MP:0000613 abnormal salivary gland morphology IEA N RGD:5509061 20200402 MGI 1313939 Bmerb1 bMERB domain containing 1 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20200402 MGI 1313939 Bmerb1 bMERB domain containing 1 gene MP:0000642 enlarged adrenal glands IEA N RGD:5509061 20200402 MGI 1313939 Bmerb1 bMERB domain containing 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 1313939 Bmerb1 bMERB domain containing 1 gene MP:0010574 dilated aorta IEA N RGD:5509061 20240523 MGI 1313941 Ilf2 interleukin enhancer binding factor 2 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:20051514 1313947 Upf1 UPF1 RNA helicase and ATPase gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:11152657 1313947 Upf1 UPF1 RNA helicase and ATPase gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11152657 1313947 Upf1 UPF1 RNA helicase and ATPase gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20141003 MGI PMID:11152657 1313947 Upf1 UPF1 RNA helicase and ATPase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11152657 1313950 Adam23 a disintegrin and metallopeptidase domain 23 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11431694 1313950 Adam23 a disintegrin and metallopeptidase domain 23 gene MP:0000745 tremors IAGP N RGD:5509061 20150205 MGI PMID:24715463 1313950 Adam23 a disintegrin and metallopeptidase domain 23 gene MP:0000745 tremors IAGP N RGD:5509061 20230330 MGI PMID:36828548 1313950 Adam23 a disintegrin and metallopeptidase domain 23 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11431694 1313950 Adam23 a disintegrin and metallopeptidase domain 23 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20230330 MGI PMID:36828548 1313950 Adam23 a disintegrin and metallopeptidase domain 23 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230330 MGI PMID:36828548 1313950 Adam23 a disintegrin and metallopeptidase domain 23 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20160421 MGI 1313950 Adam23 a disintegrin and metallopeptidase domain 23 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20230330 MGI PMID:36828548 1313950 Adam23 a disintegrin and metallopeptidase domain 23 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20230330 MGI PMID:36828548 1313950 Adam23 a disintegrin and metallopeptidase domain 23 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11431694 1313950 Adam23 a disintegrin and metallopeptidase domain 23 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20150205 MGI PMID:24715463 1313950 Adam23 a disintegrin and metallopeptidase domain 23 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20230330 MGI PMID:36828548 1313950 Adam23 a disintegrin and metallopeptidase domain 23 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1313952 Cybrd1 cytochrome b reductase 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1313952 Cybrd1 cytochrome b reductase 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:15961514 1313952 Cybrd1 cytochrome b reductase 1 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:15961514 1313956 Tia1 cytotoxic granule-associated RNA binding protein 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:14769925 1313956 Tia1 cytotoxic granule-associated RNA binding protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14769925 1313956 Tia1 cytotoxic granule-associated RNA binding protein 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10921895 1313956 Tia1 cytotoxic granule-associated RNA binding protein 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:14769925 1313956 Tia1 cytotoxic granule-associated RNA binding protein 1 gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:14769925 1313956 Tia1 cytotoxic granule-associated RNA binding protein 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:10921895 1313956 Tia1 cytotoxic granule-associated RNA binding protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10921895 1313959 Tcte1 t-complex-associated testis expressed 1 gene MP:0001124 abnormal gametes IAGP N RGD:5509061 20180208 MGI PMID:28630322 1313959 Tcte1 t-complex-associated testis expressed 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20180208 MGI PMID:28630322 1313959 Tcte1 t-complex-associated testis expressed 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20180208 MGI PMID:28630322 1313959 Tcte1 t-complex-associated testis expressed 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20180208 MGI PMID:28630322 1313961 Stac src homology three (SH3) and cysteine rich domain gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20220519 MGI 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15041039 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0001314 cornea opacity IEA N RGD:5509061 20210520 MGI 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15041039 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:12709397 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20693420 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:24285835 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0002425 abnormal susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:10553062 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16200068 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15041039 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:8700209 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:10553062 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:15721841 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10553062 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:15041039 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:15721841 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10553062 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8700209 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15041039 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:8700209 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:8700209 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19119024 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15721841 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10553062 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:24285835 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:8700209 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:12370359 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:15041039 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:20693420 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:24285835 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0008600 decreased circulating interleukin-2 level IAGP N RGD:5509061 20141003 MGI PMID:15041039 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:24285835 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15721841 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15721841 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20693420 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:24285835 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12370359 1313965 Stat4 signal transducer and activator of transcription 4 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8700209 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:20534475 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:20534475 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:20534475 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:20534475 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:14605369 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:14605369 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:14605369 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:20534475 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0001341 absent eyelids IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:22411800 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22411800 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:22411800 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:22411800 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10926768 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:10926768 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:20080592 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10926768 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20080592 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:10926768 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10926768 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10926768 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11431694 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:11431694 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:14605369 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:14605369 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22411800 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:14605369 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:14605369 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:22411800 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:22411800 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:15777636 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:10926768 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:22411800 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:20534475 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22411800 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0005198 abnormal aqueous drainage system morphology IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0005203 abnormal trabecular meshwork morphology IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0005204 abnormal canal of Schlemm morphology IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15777636 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:20534475 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:14605369 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20534475 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0008161 increased diameter of radius IAGP N RGD:5509061 20141003 MGI PMID:20534475 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0008163 increased diameter of ulna IAGP N RGD:5509061 20141003 MGI PMID:20534475 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:14605369 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:14605369 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:20080592 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0009039 absent inferior colliculus IAGP N RGD:5509061 20141003 MGI PMID:14605369 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0009877 exostosis IAGP N RGD:5509061 20141003 MGI PMID:20534475 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0009894 absent hard palate IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20171228 MGI PMID:28445472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0010079 increased osteochondroma incidence IAGP N RGD:5509061 20141003 MGI PMID:20534475 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0010079 increased osteochondroma incidence IAGP N RGD:5509061 20171228 MGI PMID:20080592 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0010079 increased osteochondroma incidence IAGP N RGD:5509061 20171228 MGI PMID:28445472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0010714 iris coloboma IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0010719 ciliary body coloboma IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22411800 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14605369 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11431694 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10926768 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20080592 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20080592 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20080592 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0012760 decreased cranial neural crest cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:22411800 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0030443 abnormal cranial synchondrosis IAGP N RGD:5509061 20171228 MGI PMID:28445472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0030883 dislocated radius head IAGP N RGD:5509061 20181101 MGI PMID:20534475 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0031212 decreased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:19509472 1313967 Ext1 exostosin glycosyltransferase 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22411800 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:791749 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:19956733 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:791749 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0000416 sparse hair IEA N RGD:5509061 20111116 MGI 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:791749 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0000427 abnormal hair cycle IEA N RGD:5509061 20111116 MGI 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:19956733 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19956733 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:791749 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:19956733 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:19956733 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:791749 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0002991 abnormal sebaceous gland physiology IAGP N RGD:5509061 20141003 MGI PMID:19956733 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:19956733 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0003846 matted coat IEA N RGD:5509061 20111116 MGI 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0003849 greasy coat IAGP N RGD:5509061 20141003 MGI PMID:19956733 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0005114 premature hair loss IEA N RGD:5509061 20111116 MGI 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:19956733 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0008731 abnormal hair shaft melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:791749 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0008767 abnormal hair medullary septa cells IAGP N RGD:5509061 20141003 MGI PMID:791749 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0009794 sebaceous gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19956733 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0010683 dilated hair follicle infundibulum IAGP N RGD:5509061 20141003 MGI PMID:19956733 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0011194 abnormal hair follicle physiology IAGP N RGD:5509061 20141003 MGI PMID:19956733 1313970 Zdhhc21 zinc finger, DHHC domain containing 21 gene MP:0013373 increased sebum secretion IAGP N RGD:5509061 20141218 MGI PMID:19956733 1313973 Psmd2 proteasome (prosome, macropain) 26S subunit, non-ATPase, 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1313973 Psmd2 proteasome (prosome, macropain) 26S subunit, non-ATPase, 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 1313980 Tymp thymidine phosphorylase gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313980 Tymp thymidine phosphorylase gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:12077348 1313980 Tymp thymidine phosphorylase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12077348 1313980 Tymp thymidine phosphorylase gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:12077348 1313980 Tymp thymidine phosphorylase gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313980 Tymp thymidine phosphorylase gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:12077348 1313980 Tymp thymidine phosphorylase gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:12077348 1313980 Tymp thymidine phosphorylase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313980 Tymp thymidine phosphorylase gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313980 Tymp thymidine phosphorylase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313980 Tymp thymidine phosphorylase gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313980 Tymp thymidine phosphorylase gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313980 Tymp thymidine phosphorylase gene MP:0009980 abnormal cerebellum dentate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313980 Tymp thymidine phosphorylase gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:19028666 1313983 Clmp CXADR-like membrane protein gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0001265 decreased body size IEA N RGD:5509061 20170323 MGI 1313983 Clmp CXADR-like membrane protein gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20180726 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0003589 abnormal ureter physiology IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0004142 abnormal muscle tone IAGP N RGD:5509061 20180726 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0004924 abnormal behavior IEA N RGD:5509061 20170323 MGI 1313983 Clmp CXADR-like membrane protein gene MP:0006144 increased systemic arterial systolic blood pressure IEA N RGD:5509061 20170323 MGI 1313983 Clmp CXADR-like membrane protein gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0008802 abnormal intestinal smooth muscle morphology IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0009480 distended cecum IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0009642 abnormal blood homeostasis IEA N RGD:5509061 20170323 MGI 1313983 Clmp CXADR-like membrane protein gene MP:0009854 impaired gastric peristalsis IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0011082 abnormal gastrointestinal motility IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180726 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20200310 MGI 1313983 Clmp CXADR-like membrane protein gene MP:0011426 abnormal ureter smooth muscle morphology IAGP N RGD:5509061 20180726 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0011480 impaired ureteric peristalsis IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0013862 abnormal cecum position IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0013954 increased intestine length IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0014022 abnormal duodenum topology IAGP N RGD:5509061 20180719 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0014023 abnormal intestine placement IAGP N RGD:5509061 20180726 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0014279 abnormal intestinal rotation IAGP N RGD:5509061 20230810 MGI PMID:29361518 1313983 Clmp CXADR-like membrane protein gene MP:0020989 increased urine lipocalin 2 level IAGP N RGD:5509061 20211216 MGI PMID:29361518 1313985 Pxn paxillin gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:11784865 1313985 Pxn paxillin gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:11784865 1313985 Pxn paxillin gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:11784865 1313985 Pxn paxillin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11784865 1313985 Pxn paxillin gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:11784865 1313985 Pxn paxillin gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:11784865 1313985 Pxn paxillin gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:11784865 1313985 Pxn paxillin gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:11784865 1313985 Pxn paxillin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11784865 1313985 Pxn paxillin gene MP:0012499 absent cardiogenic plate IAGP N RGD:5509061 20141003 MGI PMID:11784865 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17127714 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:22393014 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001203 increased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:17127714 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001203 increased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:7675084 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:16988713 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:16988713 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17127714 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16988713 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12509261 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16141330 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22393014 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22393014 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22393014 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:22393014 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22393014 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17326724 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22393014 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0001999 photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:7675084 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11454706 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16988713 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16141330 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16141330 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12509261 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16141330 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:17326724 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15533840 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:11454706 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:22393014 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16988713 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:12509261 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:7675084 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:17326724 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:22393014 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7675084 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16141330 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:12555660 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:15533840 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:17326724 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:19841728 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22393014 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0009796 abnormal base-excision repair IAGP N RGD:5509061 20141003 MGI PMID:17326724 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22393014 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17326724 1313987 Xpc xeroderma pigmentosum, complementation group C gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17326724 1313989 Mylip myosin regulatory light chain interacting protein gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 1313989 Mylip myosin regulatory light chain interacting protein gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1313989 Mylip myosin regulatory light chain interacting protein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1313989 Mylip myosin regulatory light chain interacting protein gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1313989 Mylip myosin regulatory light chain interacting protein gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1313991 Ebna1bp2 EBNA1 binding protein 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1313991 Ebna1bp2 EBNA1 binding protein 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230119 MGI 1313991 Ebna1bp2 EBNA1 binding protein 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230119 MGI 1313991 Ebna1bp2 EBNA1 binding protein 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230119 MGI 1313991 Ebna1bp2 EBNA1 binding protein 2 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241010 MGI 1313991 Ebna1bp2 EBNA1 binding protein 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1313991 Ebna1bp2 EBNA1 binding protein 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241017 MGI 1313991 Ebna1bp2 EBNA1 binding protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1313991 Ebna1bp2 EBNA1 binding protein 2 gene MP:0012111 failure of morula compaction IEA N RGD:5509061 20241010 MGI 1313991 Ebna1bp2 EBNA1 binding protein 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230119 MGI 1313994 Nusap1 nucleolar and spindle associated protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20807801 1313994 Nusap1 nucleolar and spindle associated protein 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:20807801 1313994 Nusap1 nucleolar and spindle associated protein 1 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:20807801 1313994 Nusap1 nucleolar and spindle associated protein 1 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:20807801 1313994 Nusap1 nucleolar and spindle associated protein 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20807801 1313994 Nusap1 nucleolar and spindle associated protein 1 gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:20807801 1313994 Nusap1 nucleolar and spindle associated protein 1 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:20807801 1313994 Nusap1 nucleolar and spindle associated protein 1 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20807801 1313994 Nusap1 nucleolar and spindle associated protein 1 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20807801 1313999 Cpsf3 cleavage and polyadenylation specificity factor 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1313999 Cpsf3 cleavage and polyadenylation specificity factor 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1313999 Cpsf3 cleavage and polyadenylation specificity factor 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1313999 Cpsf3 cleavage and polyadenylation specificity factor 3 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141127 MGI PMID:25296918 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0000754 paresis IAGP N RGD:5509061 20141127 MGI PMID:25296918 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141127 MGI PMID:25296918 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18560593 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141127 MGI PMID:25296918 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19492057 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:22265660 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141127 MGI PMID:25296918 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19492057 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141127 MGI PMID:25296918 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22265660 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17563363 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:17563363 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0001661 extended life span IAGP N RGD:5509061 20141127 MGI PMID:25296918 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:22265660 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:22265660 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141127 MGI PMID:25296918 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180215 MGI PMID:28360124 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20190314 MGI PMID:30578322 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:22265660 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141127 MGI PMID:25296918 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19285945 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141127 MGI PMID:25296918 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18560593 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20190314 MGI PMID:30578322 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21421046 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20180215 MGI PMID:28360124 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:17563363 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:21385841 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:21421046 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0003908 decreased stereotypic behavior IAGP N RGD:5509061 20141127 MGI PMID:25296918 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19285945 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21421046 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:18560593 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21385841 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20180215 MGI PMID:28360124 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:17563363 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:19492057 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:21249202 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:21385841 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:22265660 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20150402 MGI PMID:25609609 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:19492057 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:21249202 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:21385841 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141127 MGI PMID:25296918 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20141127 MGI PMID:25296918 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:21249202 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21249202 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:21249202 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0008830 abnormal nucleolus morphology IAGP N RGD:5509061 20180215 MGI PMID:28360124 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210520 MGI 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:21421046 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22265660 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:19285945 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:19492057 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:19492057 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:19285945 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:19492057 1314002 Pink1 PTEN induced putative kinase 1 gene MP:0011975 neuronal cytoplasmic inclusions IAGP N RGD:5509061 20150402 MGI PMID:25609609 1314004 Rbm22 RNA binding motif protein 22 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20230601 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20201022 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0003049 abnormal lumbar vertebrae morphology IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0003050 abnormal sacral vertebrae morphology IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210520 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0009709 hydrometra IEA N RGD:5509061 20210826 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210520 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1314004 Rbm22 RNA binding motif protein 22 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1314006 Casp8ap2 caspase 8 associated protein 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21725362 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:21795391 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:21795391 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:21998026 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:19154719 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:21795391 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:21998026 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:21998026 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:21795391 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:21795391 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21998026 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:19154719 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19154719 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:21998026 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0004612 fusion of vertebral bodies IAGP N RGD:5509061 20141003 MGI PMID:21998026 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:21998026 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:21998026 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0004622 sacral vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:21998026 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:21998026 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:21795391 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:21998026 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19154719 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:21498671 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0012670 prolonged somite segmentation clock period IAGP N RGD:5509061 20141003 MGI PMID:21795391 1314007 Nrarp Notch-regulated ankyrin repeat protein gene MP:0020316 decreased vascular endothelial cell proliferation IAGP N RGD:5509061 20160616 MGI PMID:19154719 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20191226 MGI PMID:26987296 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0001265 decreased body size IEA N RGD:5509061 20141003 MGI 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20160519 MGI PMID:24949970 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20220811 MGI 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0002083 premature death IEA N RGD:5509061 20141003 MGI 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20141003 MGI 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:24949970 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20160519 MGI PMID:24949970 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20220811 MGI 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20160519 MGI PMID:24949970 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20160519 MGI PMID:24949970 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20160519 MGI PMID:24949970 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0005287 narrow eye opening IEA N RGD:5509061 20141003 MGI 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20160519 MGI PMID:24949970 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20160519 MGI PMID:24949970 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20160519 MGI PMID:24949970 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0006325 impaired hearing IEA N RGD:5509061 20141003 MGI 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20160519 MGI PMID:24949970 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0011090 perinatal lethality, incomplete penetrance IEA N RGD:5509061 20141003 MGI 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20141003 MGI 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20160519 MGI PMID:24949970 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20160519 MGI PMID:24949970 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20141003 MGI 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0013179 wavy tail IEA N RGD:5509061 20141003 MGI 1314008 Clec16a C-type lectin domain family 16, member A gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20160519 MGI PMID:24949970 1314014 Inpp5f inositol polyphosphate-5-phosphatase F gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19875726 1314014 Inpp5f inositol polyphosphate-5-phosphatase F gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19875726 1314014 Inpp5f inositol polyphosphate-5-phosphatase F gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19875726 1314014 Inpp5f inositol polyphosphate-5-phosphatase F gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:19875726 1314018 Atmin ATM interactor gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20889973 1314018 Atmin ATM interactor gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19235720 1314018 Atmin ATM interactor gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:20889973 1314018 Atmin ATM interactor gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:19235720 1314018 Atmin ATM interactor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22891272 1314018 Atmin ATM interactor gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:22891272 1314018 Atmin ATM interactor gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19235720 1314018 Atmin ATM interactor gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20889973 1314018 Atmin ATM interactor gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20975950 1314018 Atmin ATM interactor gene MP:0000914 exencephaly IAGP N RGD:5509061 20150409 MGI PMID:25294941 1314018 Atmin ATM interactor gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:19235720 1314018 Atmin ATM interactor gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:20975950 1314018 Atmin ATM interactor gene MP:0001181 absent lungs IAGP N RGD:5509061 20150416 MGI PMID:25294941 1314018 Atmin ATM interactor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20889973 1314018 Atmin ATM interactor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20150409 MGI PMID:25294941 1314018 Atmin ATM interactor gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20889973 1314018 Atmin ATM interactor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20889973 1314018 Atmin ATM interactor gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19235720 1314018 Atmin ATM interactor gene MP:0001785 edema IAGP N RGD:5509061 20150409 MGI PMID:25294941 1314018 Atmin ATM interactor gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20975950 1314018 Atmin ATM interactor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20889973 1314018 Atmin ATM interactor gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:19235720 1314018 Atmin ATM interactor gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22891272 1314018 Atmin ATM interactor gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20160414 MGI PMID:26832406 1314018 Atmin ATM interactor gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:20889973 1314018 Atmin ATM interactor gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22891272 1314018 Atmin ATM interactor gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:19235720 1314018 Atmin ATM interactor gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:19235720 1314018 Atmin ATM interactor gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1314018 Atmin ATM interactor gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:24852369 1314018 Atmin ATM interactor gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:19235720 1314018 Atmin ATM interactor gene MP:0003115 abnormal respiratory system development IAGP N RGD:5509061 20141003 MGI PMID:20975950 1314018 Atmin ATM interactor gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1314018 Atmin ATM interactor gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:19235720 1314018 Atmin ATM interactor gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20150409 MGI PMID:25294941 1314018 Atmin ATM interactor gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:20889973 1314018 Atmin ATM interactor gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:20889973 1314018 Atmin ATM interactor gene MP:0003641 small lung IAGP N RGD:5509061 20150409 MGI PMID:25294941 1314018 Atmin ATM interactor gene MP:0004131 abnormal motile primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:19235720 1314018 Atmin ATM interactor gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:19235720 1314018 Atmin ATM interactor gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20150409 MGI PMID:25294941 1314018 Atmin ATM interactor gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:19235720 1314018 Atmin ATM interactor gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20975950 1314018 Atmin ATM interactor gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:24852369 1314018 Atmin ATM interactor gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22891272 1314018 Atmin ATM interactor gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22891272 1314018 Atmin ATM interactor gene MP:0004967 abnormal kidney epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24852369 1314018 Atmin ATM interactor gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1314018 Atmin ATM interactor gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1314018 Atmin ATM interactor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1314018 Atmin ATM interactor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160414 MGI PMID:26832406 1314018 Atmin ATM interactor gene MP:0005262 coloboma IAGP N RGD:5509061 20150409 MGI PMID:25294941 1314018 Atmin ATM interactor gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20889973 1314018 Atmin ATM interactor gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:20975950 1314018 Atmin ATM interactor gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20150409 MGI PMID:25294941 1314018 Atmin ATM interactor gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20889973 1314018 Atmin ATM interactor gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20975950 1314018 Atmin ATM interactor gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1314018 Atmin ATM interactor gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1314018 Atmin ATM interactor gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1314018 Atmin ATM interactor gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1314018 Atmin ATM interactor gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20160414 MGI PMID:26832406 1314018 Atmin ATM interactor gene MP:0008404 increased cellular sensitivity to methylmethanesulfonate IAGP N RGD:5509061 20141003 MGI PMID:20975950 1314018 Atmin ATM interactor gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:20975950 1314018 Atmin ATM interactor gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160414 MGI PMID:26832406 1314018 Atmin ATM interactor gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20160414 MGI PMID:26832406 1314018 Atmin ATM interactor gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:20889973 1314018 Atmin ATM interactor gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:20975950 1314018 Atmin ATM interactor gene MP:0009796 abnormal base-excision repair IAGP N RGD:5509061 20141003 MGI PMID:20975950 1314018 Atmin ATM interactor gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20160414 MGI PMID:26832406 1314018 Atmin ATM interactor gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20160414 MGI PMID:26832406 1314018 Atmin ATM interactor gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:19235720 1314018 Atmin ATM interactor gene MP:0010885 absent trachea IAGP N RGD:5509061 20150212 MGI PMID:20975950 1314018 Atmin ATM interactor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20889973 1314018 Atmin ATM interactor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20975950 1314018 Atmin ATM interactor gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20975950 1314018 Atmin ATM interactor gene MP:0011998 decreased embryonic cilium length IAGP N RGD:5509061 20150409 MGI PMID:25294941 1314018 Atmin ATM interactor gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160414 MGI PMID:26832406 1314018 Atmin ATM interactor gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20150409 MGI PMID:25294941 1314018 Atmin ATM interactor gene MP:0013213 abnormal embryonic neuroepithelium primary cilium morphology IAGP N RGD:5509061 20150409 MGI PMID:25294941 1314018 Atmin ATM interactor gene MP:0013496 abnormal trachea development IAGP N RGD:5509061 20150212 MGI PMID:20975950 1314018 Atmin ATM interactor gene MP:0030169 thick upper lip IAGP N RGD:5509061 20171005 MGI PMID:25294941 1314020 Snx10 sorting nexin 10 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0001258 decreased body length IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0002083 premature death IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1314020 Snx10 sorting nexin 10 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0003116 rickets IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0005190 osteomyelitis IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0009445 osteomalacia IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0010926 increased osteoid volume IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0012336 decreased vitamin D level IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0012336 decreased vitamin D level IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0013639 decreased bone stiffness IAGP N RGD:5509061 20151112 MGI PMID:25811986 1314020 Snx10 sorting nexin 10 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0030505 tooth impaction IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314020 Snx10 sorting nexin 10 gene MP:0030610 absent teeth IAGP N RGD:5509061 20200730 MGI PMID:32278070 1314022 Hmgxb4 HMG box domain containing 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240613 MGI PMID:33563757 1314022 Hmgxb4 HMG box domain containing 4 gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20240613 MGI PMID:33563757 1314022 Hmgxb4 HMG box domain containing 4 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20240613 MGI PMID:33563757 1314022 Hmgxb4 HMG box domain containing 4 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20240613 MGI PMID:33563757 1314022 Hmgxb4 HMG box domain containing 4 gene MP:0011077 decreased macrophage nitric oxide production IAGP N RGD:5509061 20240613 MGI PMID:33563757 1314024 Elmo2 engulfment and cell motility 2 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20231109 MGI PMID:36400788 1314024 Elmo2 engulfment and cell motility 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20231109 MGI PMID:36400788 1314024 Elmo2 engulfment and cell motility 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20231109 MGI PMID:36400788 1314024 Elmo2 engulfment and cell motility 2 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20231109 MGI PMID:36400788 1314024 Elmo2 engulfment and cell motility 2 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20231109 MGI PMID:36400788 1314024 Elmo2 engulfment and cell motility 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36400788 1314024 Elmo2 engulfment and cell motility 2 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36400788 1314024 Elmo2 engulfment and cell motility 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36400788 1314024 Elmo2 engulfment and cell motility 2 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36400788 1314024 Elmo2 engulfment and cell motility 2 gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20231109 MGI PMID:36400788 1314024 Elmo2 engulfment and cell motility 2 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20231109 MGI PMID:36400788 1314024 Elmo2 engulfment and cell motility 2 gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20231109 MGI PMID:36400788 1314026 Manba mannosidase, beta A, lysosomal gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16377659 1314026 Manba mannosidase, beta A, lysosomal gene MP:0000798 abnormal frontal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:16377659 1314026 Manba mannosidase, beta A, lysosomal gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:16377659 1314026 Manba mannosidase, beta A, lysosomal gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20141003 MGI PMID:16377659 1314026 Manba mannosidase, beta A, lysosomal gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:16377659 1314026 Manba mannosidase, beta A, lysosomal gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:16377659 1314026 Manba mannosidase, beta A, lysosomal gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16377659 1314026 Manba mannosidase, beta A, lysosomal gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:16377659 1314026 Manba mannosidase, beta A, lysosomal gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:16377659 1314026 Manba mannosidase, beta A, lysosomal gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:16377659 1314026 Manba mannosidase, beta A, lysosomal gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16377659 1314026 Manba mannosidase, beta A, lysosomal gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16377659 1314026 Manba mannosidase, beta A, lysosomal gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16377659 1314026 Manba mannosidase, beta A, lysosomal gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16377659 1314026 Manba mannosidase, beta A, lysosomal gene MP:0009979 abnormal cerebellum deep nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16377659 1314026 Manba mannosidase, beta A, lysosomal gene MP:0031148 abnormal liver sinusoidal endothelial cell morphology IAGP N RGD:5509061 20201015 MGI PMID:16377659 1314028 Plek2 pleckstrin 2 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210128 MGI 1314028 Plek2 pleckstrin 2 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20190905 MGI PMID:29202466 1314028 Plek2 pleckstrin 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20190905 MGI PMID:29202466 1314028 Plek2 pleckstrin 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20190905 MGI PMID:29202466 1314028 Plek2 pleckstrin 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20190905 MGI PMID:29202466 1314028 Plek2 pleckstrin 2 gene MP:0001577 anemia IAGP N RGD:5509061 20190905 MGI PMID:29202466 1314028 Plek2 pleckstrin 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1314028 Plek2 pleckstrin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20190905 MGI PMID:29202466 1314028 Plek2 pleckstrin 2 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20190905 MGI PMID:29202466 1314028 Plek2 pleckstrin 2 gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20190905 MGI PMID:29202466 1314028 Plek2 pleckstrin 2 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20190905 MGI PMID:29202466 1314028 Plek2 pleckstrin 2 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20190905 MGI PMID:29202466 1314028 Plek2 pleckstrin 2 gene MP:0011913 abnormal reticulocyte cell number IAGP N RGD:5509061 20190905 MGI PMID:29202466 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20171221 MGI PMID:28578315 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200102 MGI PMID:28578316 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200102 MGI PMID:28578316 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20171221 MGI PMID:28578315 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20200102 MGI PMID:28578316 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20171221 MGI PMID:28578315 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20171221 MGI PMID:28578315 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20200102 MGI PMID:28578316 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20200102 MGI PMID:28578316 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20171221 MGI PMID:28578315 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20200102 MGI PMID:28578316 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0005571 decreased lactate dehydrogenase level IEA N RGD:5509061 20160804 MGI 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20171221 MGI PMID:28578315 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200102 MGI PMID:28578316 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0008581 disorganized photoreceptor inner segment IAGP N RGD:5509061 20200102 MGI PMID:28578316 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20200102 MGI PMID:28578316 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20200102 MGI PMID:28578316 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200102 MGI PMID:28578316 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20171221 MGI PMID:28578315 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160804 MGI 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200102 MGI PMID:28578316 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200102 MGI PMID:28578316 1314030 Agpat3 1-acylglycerol-3-phosphate O-acyltransferase 3 gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20200102 MGI PMID:28578316 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:17215307 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20200514 MGI 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:17215307 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17215307 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17215307 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17215307 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17215307 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17215307 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:17215307 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23207902 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23207902 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23207902 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23207902 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:17215307 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:17215307 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17215307 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17215307 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20200514 MGI 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23207902 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0011246 abnormal fetal liver hematopoietic progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23207902 1314032 Scmh1 sex comb on midleg homolog 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:17215307 1314034 Wdr1 WD repeat domain 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12955145 1314034 Wdr1 WD repeat domain 1 gene MP:0001849 ear inflammation IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0002083 premature death IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151112 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20170803 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0003405 abnormal platelet shape IAGP N RGD:5509061 20170803 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0004721 abnormal platelet dense granule morphology IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0010505 abnormal T wave IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0010570 prolonged ST segment IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20151015 MGI PMID:24840128 1314034 Wdr1 WD repeat domain 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314034 Wdr1 WD repeat domain 1 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1314034 Wdr1 WD repeat domain 1 gene MP:0014060 abnormal platelet alpha-granule morphology IAGP N RGD:5509061 20170803 MGI PMID:17515402 1314034 Wdr1 WD repeat domain 1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:24840128 1314038 Snx8 sorting nexin 8 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20181227 MGI 1314038 Snx8 sorting nexin 8 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210520 MGI 1314038 Snx8 sorting nexin 8 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20210708 MGI PMID:29180417 1314038 Snx8 sorting nexin 8 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20210708 MGI PMID:29180417 1314038 Snx8 sorting nexin 8 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20210708 MGI PMID:29180417 1314038 Snx8 sorting nexin 8 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1314038 Snx8 sorting nexin 8 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1314038 Snx8 sorting nexin 8 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1314038 Snx8 sorting nexin 8 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 1314038 Snx8 sorting nexin 8 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1314038 Snx8 sorting nexin 8 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20210708 MGI PMID:29180417 1314038 Snx8 sorting nexin 8 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20210708 MGI PMID:29180417 1314038 Snx8 sorting nexin 8 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20210708 MGI PMID:29180417 1314038 Snx8 sorting nexin 8 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20181227 MGI 1314038 Snx8 sorting nexin 8 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20210708 MGI PMID:29180417 1314038 Snx8 sorting nexin 8 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20210708 MGI PMID:29180417 1314038 Snx8 sorting nexin 8 gene MP:0031219 decreased circulating CXCL10 level IAGP N RGD:5509061 20210708 MGI PMID:29180417 1314038 Snx8 sorting nexin 8 gene MP:0031222 decreased CXCL10 secretion IAGP N RGD:5509061 20210708 MGI PMID:29180417 1314040 Krt36 keratin 36 gene MP:0000763 abnormal filiform papillae morphology IEA N RGD:5509061 20170420 MGI 1314040 Krt36 keratin 36 gene MP:0001242 hyperkeratosis IEA N RGD:5509061 20170420 MGI 1314040 Krt36 keratin 36 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20170420 MGI 1314042 Wbp1l WW domain binding protein 1 like gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210520 MGI 1314042 Wbp1l WW domain binding protein 1 like gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1314042 Wbp1l WW domain binding protein 1 like gene MP:0001488 increased startle reflex IEA N RGD:5509061 20201022 MGI 1314042 Wbp1l WW domain binding protein 1 like gene MP:0002403 abnormal pre-B cell morphology IAGP N RGD:5509061 20201015 MGI PMID:31845480 1314042 Wbp1l WW domain binding protein 1 like gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20200402 MGI 1314042 Wbp1l WW domain binding protein 1 like gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20201015 MGI PMID:31845480 1314042 Wbp1l WW domain binding protein 1 like gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20201015 MGI PMID:31845480 1314042 Wbp1l WW domain binding protein 1 like gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20201015 MGI PMID:31845480 1314042 Wbp1l WW domain binding protein 1 like gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20201015 MGI PMID:31845480 1314042 Wbp1l WW domain binding protein 1 like gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1314042 Wbp1l WW domain binding protein 1 like gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210520 MGI 1314042 Wbp1l WW domain binding protein 1 like gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210520 MGI 1314042 Wbp1l WW domain binding protein 1 like gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20201015 MGI PMID:31845480 1314042 Wbp1l WW domain binding protein 1 like gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20201015 MGI PMID:31845480 1314042 Wbp1l WW domain binding protein 1 like gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20201015 MGI PMID:31845480 1314042 Wbp1l WW domain binding protein 1 like gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20201015 MGI PMID:31845480 1314042 Wbp1l WW domain binding protein 1 like gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20190502 MGI 1314042 Wbp1l WW domain binding protein 1 like gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20201015 MGI PMID:31845480 1314042 Wbp1l WW domain binding protein 1 like gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1314042 Wbp1l WW domain binding protein 1 like gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20211021 MGI 1314042 Wbp1l WW domain binding protein 1 like gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20200402 MGI 1314042 Wbp1l WW domain binding protein 1 like gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 1314046 Trim21 tripartite motif-containing 21 gene MP:0000622 increased salivation IAGP N RGD:5509061 20240516 MGI PMID:33957127 1314046 Trim21 tripartite motif-containing 21 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19635858 1314046 Trim21 tripartite motif-containing 21 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19635858 1314046 Trim21 tripartite motif-containing 21 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:19635858 1314046 Trim21 tripartite motif-containing 21 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:19635858 1314046 Trim21 tripartite motif-containing 21 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:19635858 1314046 Trim21 tripartite motif-containing 21 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:19635858 1314046 Trim21 tripartite motif-containing 21 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:19494276 1314046 Trim21 tripartite motif-containing 21 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:19635858 1314046 Trim21 tripartite motif-containing 21 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:19635858 1314046 Trim21 tripartite motif-containing 21 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:19635858 1314046 Trim21 tripartite motif-containing 21 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19635858 1314046 Trim21 tripartite motif-containing 21 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19635858 1314049 Ttc39b tetratricopeptide repeat domain 39B gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1314049 Ttc39b tetratricopeptide repeat domain 39B gene MP:0005505 thrombocytosis IEA N RGD:5509061 20160804 MGI 1314049 Ttc39b tetratricopeptide repeat domain 39B gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20160804 MGI 1314051 Mboat2 membrane bound O-acyltransferase domain containing 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1314051 Mboat2 membrane bound O-acyltransferase domain containing 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1314051 Mboat2 membrane bound O-acyltransferase domain containing 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1314051 Mboat2 membrane bound O-acyltransferase domain containing 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1314051 Mboat2 membrane bound O-acyltransferase domain containing 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1314051 Mboat2 membrane bound O-acyltransferase domain containing 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1314051 Mboat2 membrane bound O-acyltransferase domain containing 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 1314051 Mboat2 membrane bound O-acyltransferase domain containing 2 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20220811 MGI 1314057 Hoxc9 homeobox C9 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314057 Hoxc9 homeobox C9 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:7547473 1314057 Hoxc9 homeobox C9 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:7547473 1314057 Hoxc9 homeobox C9 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:7547473 1314057 Hoxc9 homeobox C9 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:7547473 1314057 Hoxc9 homeobox C9 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314057 Hoxc9 homeobox C9 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7547473 1314057 Hoxc9 homeobox C9 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314057 Hoxc9 homeobox C9 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314057 Hoxc9 homeobox C9 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314057 Hoxc9 homeobox C9 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7547473 1314057 Hoxc9 homeobox C9 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314057 Hoxc9 homeobox C9 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314057 Hoxc9 homeobox C9 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314057 Hoxc9 homeobox C9 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7547473 1314057 Hoxc9 homeobox C9 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314057 Hoxc9 homeobox C9 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7547473 1314057 Hoxc9 homeobox C9 gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314057 Hoxc9 homeobox C9 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:7547473 1314057 Hoxc9 homeobox C9 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:7547473 1314057 Hoxc9 homeobox C9 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314057 Hoxc9 homeobox C9 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314059 Snx15 sorting nexin 15 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1314059 Snx15 sorting nexin 15 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20211021 MGI 1314059 Snx15 sorting nexin 15 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201231 MGI 1314059 Snx15 sorting nexin 15 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20201022 MGI 1314059 Snx15 sorting nexin 15 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 1314059 Snx15 sorting nexin 15 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1314059 Snx15 sorting nexin 15 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1314061 Dusp2 dual specificity phosphatase 2 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16474395 1314061 Dusp2 dual specificity phosphatase 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16474395 1314061 Dusp2 dual specificity phosphatase 2 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:16474395 1314061 Dusp2 dual specificity phosphatase 2 gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20141003 MGI PMID:16474395 1314065 Stra6l STRA6-like gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1314065 Stra6l STRA6-like gene MP:0001314 cornea opacity IEA N RGD:5509061 20170105 MGI 1314065 Stra6l STRA6-like gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1314065 Stra6l STRA6-like gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1314065 Stra6l STRA6-like gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1314065 Stra6l STRA6-like gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1314065 Stra6l STRA6-like gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1314065 Stra6l STRA6-like gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1314073 Osr2 odd-skipped related 2 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:15175245 1314073 Osr2 odd-skipped related 2 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:19389375 1314073 Osr2 odd-skipped related 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19341725 1314073 Osr2 odd-skipped related 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19631205 1314073 Osr2 odd-skipped related 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:24785830 1314073 Osr2 odd-skipped related 2 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:19631205 1314073 Osr2 odd-skipped related 2 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:21420399 1314073 Osr2 odd-skipped related 2 gene MP:0000128 growth retardation of molars IAGP N RGD:5509061 20141003 MGI PMID:19631205 1314073 Osr2 odd-skipped related 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:19341725 1314073 Osr2 odd-skipped related 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20170921 MGI PMID:19341725 1314073 Osr2 odd-skipped related 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:19389375 1314073 Osr2 odd-skipped related 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15175245 1314073 Osr2 odd-skipped related 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:19389375 1314073 Osr2 odd-skipped related 2 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15175245 1314073 Osr2 odd-skipped related 2 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19631205 1314073 Osr2 odd-skipped related 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17941042 1314073 Osr2 odd-skipped related 2 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:21262216 1314073 Osr2 odd-skipped related 2 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:21262216 1314073 Osr2 odd-skipped related 2 gene MP:0003190 fused synovial joints IAGP N RGD:5509061 20141003 MGI PMID:21262216 1314073 Osr2 odd-skipped related 2 gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20141003 MGI PMID:19389375 1314073 Osr2 odd-skipped related 2 gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20141003 MGI PMID:21420399 1314073 Osr2 odd-skipped related 2 gene MP:0005359 growth retardation of incisors IAGP N RGD:5509061 20141003 MGI PMID:19631205 1314073 Osr2 odd-skipped related 2 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:19389375 1314073 Osr2 odd-skipped related 2 gene MP:0009263 abnormal eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:19389375 1314073 Osr2 odd-skipped related 2 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:19389375 1314073 Osr2 odd-skipped related 2 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:21262216 1314073 Osr2 odd-skipped related 2 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221027 MGI PMID:34557486 1314073 Osr2 odd-skipped related 2 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34557486 1314073 Osr2 odd-skipped related 2 gene MP:0009884 palatal shelf fusion with tongue or mandible IAGP N RGD:5509061 20180201 MGI PMID:24785830 1314073 Osr2 odd-skipped related 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:15175245 1314073 Osr2 odd-skipped related 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20180201 MGI PMID:24785830 1314073 Osr2 odd-skipped related 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15175245 1314073 Osr2 odd-skipped related 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:19631205 1314073 Osr2 odd-skipped related 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:21420399 1314073 Osr2 odd-skipped related 2 gene MP:0010864 abnormal enamel knot morphology IAGP N RGD:5509061 20171221 MGI PMID:19631205 1314073 Osr2 odd-skipped related 2 gene MP:0011087 neonatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1314073 Osr2 odd-skipped related 2 gene MP:0012163 abnormal dental mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:19631205 1314073 Osr2 odd-skipped related 2 gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20230302 MGI PMID:19389375 1314073 Osr2 odd-skipped related 2 gene MP:0021202 abnormal palatopharyngeus muscle morphology IAGP N RGD:5509061 20221103 MGI PMID:34557486 1314073 Osr2 odd-skipped related 2 gene MP:0021203 abnormal palatine aponeurosis morphology IAGP N RGD:5509061 20221103 MGI PMID:34557486 1314073 Osr2 odd-skipped related 2 gene MP:0021204 abnormal superior pharyngeal constrictor muscle morphology IAGP N RGD:5509061 20221103 MGI PMID:34557486 1314073 Osr2 odd-skipped related 2 gene MP:0021210 bilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:15175245 1314073 Osr2 odd-skipped related 2 gene MP:0021210 bilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:19389375 1314073 Osr2 odd-skipped related 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:15175245 1314073 Osr2 odd-skipped related 2 gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:21420399 1314073 Osr2 odd-skipped related 2 gene MP:0030293 small tensor veli palatini muscle IAGP N RGD:5509061 20221027 MGI PMID:34557486 1314073 Osr2 odd-skipped related 2 gene MP:0030295 small levator veli palatini muscle IAGP N RGD:5509061 20221027 MGI PMID:34557486 1314079 Kera keratocan gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17911102 1314079 Kera keratocan gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17911102 1314079 Kera keratocan gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:12665512 1314079 Kera keratocan gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20201231 MGI 1314079 Kera keratocan gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:12665512 1314079 Kera keratocan gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:17911102 1314088 Cep20 centrosomal protein 20 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314088 Cep20 centrosomal protein 20 gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20220505 MGI PMID:33686659 1314091 Tpte transmembrane phosphatase with tensin homology gene MP:0000160 kyphosis IEA N RGD:5509061 20230601 MGI 1314091 Tpte transmembrane phosphatase with tensin homology gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20201015 MGI PMID:31776261 1314091 Tpte transmembrane phosphatase with tensin homology gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1314091 Tpte transmembrane phosphatase with tensin homology gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20201015 MGI PMID:31776261 1314091 Tpte transmembrane phosphatase with tensin homology gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20230601 MGI 1314091 Tpte transmembrane phosphatase with tensin homology gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20201015 MGI PMID:31776261 1314091 Tpte transmembrane phosphatase with tensin homology gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20201015 MGI PMID:31776261 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20220324 MGI PMID:35216179 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20230330 MGI PMID:36512060 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20230330 MGI PMID:36512060 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0001260 increased body weight IAGP N RGD:5509061 20220324 MGI PMID:35216179 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20230330 MGI PMID:36512060 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20220324 MGI PMID:35216179 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20230330 MGI PMID:36512060 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20230330 MGI PMID:36512060 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20230330 MGI PMID:36512060 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20230330 MGI PMID:36512060 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20230330 MGI PMID:36512060 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20230330 MGI PMID:36512060 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20230330 MGI PMID:36512060 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20230330 MGI PMID:36512060 1314093 Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20230330 MGI PMID:36512060 1314095 Cndp2 CNDP dipeptidase 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1314095 Cndp2 CNDP dipeptidase 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1314095 Cndp2 CNDP dipeptidase 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1314095 Cndp2 CNDP dipeptidase 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1314095 Cndp2 CNDP dipeptidase 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1314095 Cndp2 CNDP dipeptidase 2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1314095 Cndp2 CNDP dipeptidase 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230601 MGI 1314095 Cndp2 CNDP dipeptidase 2 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210128 MGI 1314095 Cndp2 CNDP dipeptidase 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1314095 Cndp2 CNDP dipeptidase 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1314095 Cndp2 CNDP dipeptidase 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1314095 Cndp2 CNDP dipeptidase 2 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210128 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20201022 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0000553 absent radius IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0000614 absent salivary gland IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20200514 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0001181 absent lungs IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0001196 shiny skin IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0001394 circling IEA N RGD:5509061 20141003 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20141003 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0001785 edema IEA N RGD:5509061 20230601 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20230601 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210826 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0003853 dry skin IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0004197 abnormal fetal growth/weight/body size IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0004352 absent humerus IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0004475 palatine bone hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0004870 small premaxilla IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0006306 abnormal nasal pit morphology IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0008797 facial cleft IEA N RGD:5509061 20230601 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0009893 cleft primary palate IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0009893 cleft primary palate IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0009898 maxillary shelf hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0013545 cleft hard palate IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0013546 cleft soft palate IAGP N RGD:5509061 20160218 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0021210 bilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0021210 bilateral cleft palate IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:26371508 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230309 MGI PMID:32253237 1314096 Esrp1 epithelial splicing regulatory protein 1 gene MP:0031504 increased mouth width IAGP N RGD:5509061 20230810 MGI PMID:26371508 1314100 Calhm4 calcium homeostasis modulator family member 4 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1314100 Calhm4 calcium homeostasis modulator family member 4 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1314100 Calhm4 calcium homeostasis modulator family member 4 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1314105 Zgrf1 zinc finger, GRF-type containing 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1314107 Tectb tectorin beta gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17220887 1314107 Tectb tectorin beta gene MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:17220887 1314107 Tectb tectorin beta gene MP:0004591 enlarged tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:17220887 1314107 Tectb tectorin beta gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:17220887 1314107 Tectb tectorin beta gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:17220887 1314107 Tectb tectorin beta gene MP:0006384 enhanced cochlear frequency tuning IAGP N RGD:5509061 20141003 MGI PMID:17220887 1314107 Tectb tectorin beta gene MP:0013962 absent Hensen stripe IAGP N RGD:5509061 20160310 MGI PMID:17220887 1314107 Tectb tectorin beta gene MP:0014089 abnormal tectorial membrane marginal band morphology IAGP N RGD:5509061 20160421 MGI PMID:17220887 1314107 Tectb tectorin beta gene MP:0014091 abnormal tectorial membrane striated-sheet matrix morphology IAGP N RGD:5509061 20160421 MGI PMID:17220887 1314109 Rasgef1a RasGEF domain family, member 1A gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1314112 Dppa5a developmental pluripotency associated 5A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16504174 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20181227 MGI 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23179078 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:23179078 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:23179078 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23179078 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20170504 MGI 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23179078 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:23179078 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:23179078 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23179078 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23179078 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:23179078 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23179078 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20181227 MGI 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:23179078 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23179078 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23179078 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314114 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 gene MP:0011625 cystolithiasis IEA N RGD:5509061 20181227 MGI 1314116 Abcg4 ATP binding cassette subfamily G member 4 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:18039927 1314116 Abcg4 ATP binding cassette subfamily G member 4 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18039927 1314116 Abcg4 ATP binding cassette subfamily G member 4 gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20141003 MGI PMID:18039927 1314116 Abcg4 ATP binding cassette subfamily G member 4 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18039927 1314121 Caln1 calneuron 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20231019 MGI PMID:37355986 1314121 Caln1 calneuron 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20231019 MGI PMID:37355986 1314121 Caln1 calneuron 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20231019 MGI PMID:37355986 1314121 Caln1 calneuron 1 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20231019 MGI PMID:37355986 1314121 Caln1 calneuron 1 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20231019 MGI PMID:37355986 1314121 Caln1 calneuron 1 gene MP:0011149 abnormal hippocampus stratum lacunosum morphology IAGP N RGD:5509061 20231019 MGI PMID:37355986 1314121 Caln1 calneuron 1 gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20231019 MGI PMID:37355986 1314121 Caln1 calneuron 1 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20231019 MGI PMID:37355986 1314125 Spopl speckle-type BTB/POZ protein-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170518 MGI PMID:27930311 1314125 Spopl speckle-type BTB/POZ protein-like gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20150430 MGI 1314127 Arpc2 actin related protein 2/3 complex, subunit 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1314127 Arpc2 actin related protein 2/3 complex, subunit 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160804 MGI 1314127 Arpc2 actin related protein 2/3 complex, subunit 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1314127 Arpc2 actin related protein 2/3 complex, subunit 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20141003 MGI 1314127 Arpc2 actin related protein 2/3 complex, subunit 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314129 Rin3 Ras and Rab interactor 3 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20221215 MGI 1314129 Rin3 Ras and Rab interactor 3 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 1314129 Rin3 Ras and Rab interactor 3 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20211021 MGI 1314129 Rin3 Ras and Rab interactor 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170105 MGI 1314129 Rin3 Ras and Rab interactor 3 gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20211021 MGI 1314129 Rin3 Ras and Rab interactor 3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1314131 Astn2 astrotactin 2 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20180118 MGI PMID:26418459 1314131 Astn2 astrotactin 2 gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20180118 MGI PMID:26418459 1314132 Tex261 testis expressed gene 261 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20200514 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20210128 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20200514 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20200514 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210128 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200514 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200514 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20200514 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20200514 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200514 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20200514 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1314132 Tex261 testis expressed gene 261 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20200514 MGI 1314134 Fkrp fukutin related protein gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:24234655 1314134 Fkrp fukutin related protein gene MP:0000751 myopathy IAGP N RGD:5509061 20200430 MGI PMID:26574668 1314134 Fkrp fukutin related protein gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:24234655 1314134 Fkrp fukutin related protein gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20171214 MGI PMID:28859131 1314134 Fkrp fukutin related protein gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19155270 1314134 Fkrp fukutin related protein gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19155270 1314134 Fkrp fukutin related protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24234655 1314134 Fkrp fukutin related protein gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19155270 1314134 Fkrp fukutin related protein gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:24234655 1314134 Fkrp fukutin related protein gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:24234655 1314134 Fkrp fukutin related protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24234655 1314134 Fkrp fukutin related protein gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:24234655 1314134 Fkrp fukutin related protein gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:24234655 1314134 Fkrp fukutin related protein gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19155270 1314134 Fkrp fukutin related protein gene MP:0002697 abnormal eye size IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:19155270 1314134 Fkrp fukutin related protein gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20171214 MGI PMID:28859131 1314134 Fkrp fukutin related protein gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:19155270 1314134 Fkrp fukutin related protein gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200430 MGI PMID:26574668 1314134 Fkrp fukutin related protein gene MP:0003199 calcified muscle IAGP N RGD:5509061 20141003 MGI PMID:24234655 1314134 Fkrp fukutin related protein gene MP:0003381 vitreal fibroplasia IAGP N RGD:5509061 20171214 MGI PMID:28859131 1314134 Fkrp fukutin related protein gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19155270 1314134 Fkrp fukutin related protein gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20171214 MGI PMID:28859131 1314134 Fkrp fukutin related protein gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20171214 MGI PMID:28859131 1314134 Fkrp fukutin related protein gene MP:0004246 abnormal extensor digitorum longus morphology IAGP N RGD:5509061 20141003 MGI PMID:19155270 1314134 Fkrp fukutin related protein gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:24234655 1314134 Fkrp fukutin related protein gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20171214 MGI PMID:28859131 1314134 Fkrp fukutin related protein gene MP:0005623 abnormal meninges morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0008030 abnormal Cajal-Retzius cell morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0008259 abnormal optic disk morphology IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20171214 MGI PMID:28859131 1314134 Fkrp fukutin related protein gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20171214 MGI PMID:28859131 1314134 Fkrp fukutin related protein gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0009026 abnormal brain pia mater morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20200430 MGI PMID:26574668 1314134 Fkrp fukutin related protein gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20200430 MGI PMID:26574668 1314134 Fkrp fukutin related protein gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:19155270 1314134 Fkrp fukutin related protein gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:24234655 1314134 Fkrp fukutin related protein gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20171214 MGI PMID:28859131 1314134 Fkrp fukutin related protein gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:19155270 1314134 Fkrp fukutin related protein gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20200430 MGI PMID:26574668 1314134 Fkrp fukutin related protein gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:24234655 1314134 Fkrp fukutin related protein gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20200430 MGI PMID:26574668 1314134 Fkrp fukutin related protein gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:24234655 1314134 Fkrp fukutin related protein gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0009959 abnormal cerebellar hemisphere morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0010235 abnormal retina inner limiting membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24234655 1314134 Fkrp fukutin related protein gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19155270 1314134 Fkrp fukutin related protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20675713 1314134 Fkrp fukutin related protein gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20190530 MGI PMID:26306834 1314134 Fkrp fukutin related protein gene MP:0012031 abnormal b-wave amplitude IAGP N RGD:5509061 20171214 MGI PMID:28859131 1314134 Fkrp fukutin related protein gene MP:0012145 increased a-wave amplitude IAGP N RGD:5509061 20171214 MGI PMID:28859131 1314134 Fkrp fukutin related protein gene MP:0014257 embryonic lethality prior to tooth bud stage, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:26574668 1314134 Fkrp fukutin related protein gene MP:0030265 parietal bossing IAGP N RGD:5509061 20171026 MGI PMID:20675713 1314137 Dbf4 DBF4 zinc finger gene MP:0001513 limb grasping IEA N RGD:5509061 20201231 MGI 1314137 Dbf4 DBF4 zinc finger gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314137 Dbf4 DBF4 zinc finger gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1314137 Dbf4 DBF4 zinc finger gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1314142 Cdc42ep3 CDC42 effector protein 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20221215 MGI 1314142 Cdc42ep3 CDC42 effector protein 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1314144 Elf5 E74-like factor 5 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:15650748 1314144 Elf5 E74-like factor 5 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:19269284 1314144 Elf5 E74-like factor 5 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:15829518 1314144 Elf5 E74-like factor 5 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:15829518 1314144 Elf5 E74-like factor 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15829518 1314144 Elf5 E74-like factor 5 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:15650748 1314144 Elf5 E74-like factor 5 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:19269284 1314144 Elf5 E74-like factor 5 gene MP:0002583 absent extraembryonic ectoderm IAGP N RGD:5509061 20141003 MGI PMID:15829518 1314144 Elf5 E74-like factor 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15829518 1314144 Elf5 E74-like factor 5 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15829518 1314144 Elf5 E74-like factor 5 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:19269284 1314144 Elf5 E74-like factor 5 gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:15829518 1314144 Elf5 E74-like factor 5 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19269284 1314144 Elf5 E74-like factor 5 gene MP:0009593 absent chorion IAGP N RGD:5509061 20141003 MGI PMID:15829518 1314144 Elf5 E74-like factor 5 gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:15650748 1314144 Elf5 E74-like factor 5 gene MP:0010249 lactation failure IAGP N RGD:5509061 20150402 MGI PMID:19269284 1314144 Elf5 E74-like factor 5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17938949 1314144 Elf5 E74-like factor 5 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15650748 1314144 Elf5 E74-like factor 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15829518 1314151 Stk32c serine/threonine kinase 32C gene MP:0001513 limb grasping IEA N RGD:5509061 20201231 MGI 1314151 Stk32c serine/threonine kinase 32C gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20240523 MGI 1314151 Stk32c serine/threonine kinase 32C gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1314153 Zfp451 zinc finger protein 451 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1314153 Zfp451 zinc finger protein 451 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20160811 MGI 1314153 Zfp451 zinc finger protein 451 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20160811 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20200514 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0000416 sparse hair IAGP N RGD:5509061 20180628 MGI PMID:26788537 1314154 Fam83h family with sequence similarity 83, member H gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20201022 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0000746 weakness IAGP N RGD:5509061 20180628 MGI PMID:26788537 1314154 Fam83h family with sequence similarity 83, member H gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20201022 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0001147 small testis IEA N RGD:5509061 20201022 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0001192 scaly skin IAGP N RGD:5509061 20180628 MGI PMID:26788537 1314154 Fam83h family with sequence similarity 83, member H gene MP:0001265 decreased body size IAGP N RGD:5509061 20180628 MGI PMID:26788537 1314154 Fam83h family with sequence similarity 83, member H gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180628 MGI PMID:26788537 1314154 Fam83h family with sequence similarity 83, member H gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200514 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0001511 disheveled coat IAGP N RGD:5509061 20180628 MGI PMID:26788537 1314154 Fam83h family with sequence similarity 83, member H gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20201022 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0002083 premature death IAGP N RGD:5509061 20180628 MGI PMID:26788537 1314154 Fam83h family with sequence similarity 83, member H gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0002188 small heart IEA N RGD:5509061 20201022 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0003053 delayed tooth eruption IAGP N RGD:5509061 20180628 MGI PMID:26788537 1314154 Fam83h family with sequence similarity 83, member H gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210128 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20201022 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20220519 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20220519 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20211021 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180628 MGI PMID:26788537 1314154 Fam83h family with sequence similarity 83, member H gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1314154 Fam83h family with sequence similarity 83, member H gene MP:0013818 abnormal oral cavity morphology IAGP N RGD:5509061 20180628 MGI PMID:26788537 1314154 Fam83h family with sequence similarity 83, member H gene MP:0030490 periodontal pocket IAGP N RGD:5509061 20180628 MGI PMID:26788537 1314156 Snph syntaphilin gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1314156 Snph syntaphilin gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1314156 Snph syntaphilin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18191227 1314156 Snph syntaphilin gene MP:0002175 decreased brain weight IEA N RGD:5509061 20210128 MGI 1314156 Snph syntaphilin gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:18191227 1314156 Snph syntaphilin gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18191227 1314156 Snph syntaphilin gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:18191227 1314156 Snph syntaphilin gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:18191227 1314156 Snph syntaphilin gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:18191227 1314156 Snph syntaphilin gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 1314159 Asxl3 ASXL transcriptional regulator 3 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20240208 MGI PMID:32696347 1314159 Asxl3 ASXL transcriptional regulator 3 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20240208 MGI PMID:32696347 1314159 Asxl3 ASXL transcriptional regulator 3 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20240208 MGI PMID:32696347 1314159 Asxl3 ASXL transcriptional regulator 3 gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20231109 MGI PMID:36325906 1314159 Asxl3 ASXL transcriptional regulator 3 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20231109 MGI PMID:36325906 1314159 Asxl3 ASXL transcriptional regulator 3 gene MP:0004937 dilated heart IAGP N RGD:5509061 20231109 MGI PMID:36325906 1314159 Asxl3 ASXL transcriptional regulator 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20240208 MGI PMID:32696347 1314159 Asxl3 ASXL transcriptional regulator 3 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20240208 MGI PMID:32696347 1314159 Asxl3 ASXL transcriptional regulator 3 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20231109 MGI PMID:36325906 1314159 Asxl3 ASXL transcriptional regulator 3 gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20240208 MGI PMID:32696347 1314159 Asxl3 ASXL transcriptional regulator 3 gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20240208 MGI PMID:32696347 1314159 Asxl3 ASXL transcriptional regulator 3 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20240208 MGI PMID:32696347 1314159 Asxl3 ASXL transcriptional regulator 3 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20240208 MGI PMID:32696347 1314161 Pcdh18 protocadherin 18 gene MP:0000564 syndactyly IEA N RGD:5509061 20201231 MGI 1314161 Pcdh18 protocadherin 18 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210128 MGI 1314161 Pcdh18 protocadherin 18 gene MP:0001314 cornea opacity IEA N RGD:5509061 20160114 MGI 1314161 Pcdh18 protocadherin 18 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1314161 Pcdh18 protocadherin 18 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1314161 Pcdh18 protocadherin 18 gene MP:0003900 shortened QT interval IEA N RGD:5509061 20210826 MGI 1314161 Pcdh18 protocadherin 18 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160114 MGI 1314161 Pcdh18 protocadherin 18 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20240627 MGI 1314161 Pcdh18 protocadherin 18 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20150430 MGI 1314161 Pcdh18 protocadherin 18 gene MP:0010571 shortened ST segment IEA N RGD:5509061 20210128 MGI 1314161 Pcdh18 protocadherin 18 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:14988498 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:14988498 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:19016524 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14729948 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:14988498 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:19016524 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:14988498 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19016524 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:14988498 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:14988498 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:14988498 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:19016524 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19016524 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19016524 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:19016524 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:19016524 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:19016524 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:19016524 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:19016524 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19016524 1314163 Tnfsf13 tumor necrosis factor (ligand) superfamily, member 13 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:19016524 1314165 Naalad2 N-acetylated alpha-linked acidic dipeptidase 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20240718 MGI PMID:37349952 1314165 Naalad2 N-acetylated alpha-linked acidic dipeptidase 2 gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20240718 MGI PMID:37349952 1314165 Naalad2 N-acetylated alpha-linked acidic dipeptidase 2 gene MP:0030737 decreased glutamic acid level IAGP N RGD:5509061 20240718 MGI PMID:37349952 1314167 Rin2 Ras and Rab interactor 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1314171 Sirt7 sirtuin 7 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:24210820 1314171 Sirt7 sirtuin 7 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:24210820 1314171 Sirt7 sirtuin 7 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24210820 1314171 Sirt7 sirtuin 7 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:24210820 1314171 Sirt7 sirtuin 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24210820 1314171 Sirt7 sirtuin 7 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:24210820 1314171 Sirt7 sirtuin 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24210820 1314171 Sirt7 sirtuin 7 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:24210820 1314171 Sirt7 sirtuin 7 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:24210820 1314171 Sirt7 sirtuin 7 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:24210820 1314171 Sirt7 sirtuin 7 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:24210820 1314171 Sirt7 sirtuin 7 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:18239138 1314171 Sirt7 sirtuin 7 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:24210820 1314171 Sirt7 sirtuin 7 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:24210820 1314171 Sirt7 sirtuin 7 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:24210820 1314173 Gns glucosamine (N-acetyl)-6-sulfatase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180111 MGI PMID:28334745 1314173 Gns glucosamine (N-acetyl)-6-sulfatase gene MP:0002083 premature death IAGP N RGD:5509061 20180111 MGI PMID:28334745 1314173 Gns glucosamine (N-acetyl)-6-sulfatase gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20180111 MGI PMID:28334745 1314173 Gns glucosamine (N-acetyl)-6-sulfatase gene MP:0003354 astrocytosis IAGP N RGD:5509061 20180111 MGI PMID:28334745 1314173 Gns glucosamine (N-acetyl)-6-sulfatase gene MP:0008918 microgliosis IAGP N RGD:5509061 20180111 MGI PMID:28334745 1314175 Cldn12 claudin 12 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0000745 tremors IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0001258 decreased body length IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0001260 increased body weight IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1314175 Cldn12 claudin 12 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1314175 Cldn12 claudin 12 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0010511 shortened PR interval IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0011954 shortened PQ interval IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314175 Cldn12 claudin 12 gene MP:0020151 abnormal circulating non-HDL cholesterol level IAGP N RGD:5509061 20191114 MGI PMID:31511021 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20220825 MGI PMID:23968836 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230601 MGI PMID:35736367 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20230601 MGI PMID:35736367 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20220825 MGI PMID:23968836 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20230601 MGI PMID:35736367 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20220825 MGI PMID:23968836 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12756295 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20220825 MGI PMID:23968836 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20230601 MGI PMID:35736367 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19897492 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19897492 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220428 MGI PMID:29659998 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220428 MGI PMID:29659998 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220428 MGI PMID:29659998 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220428 MGI PMID:29659998 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:12756295 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20220825 MGI PMID:23968836 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20230601 MGI PMID:35736367 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20230601 MGI PMID:35736367 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220428 MGI PMID:29659998 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220428 MGI PMID:29659998 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220428 MGI PMID:29659998 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20220825 MGI PMID:23968836 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20230601 MGI PMID:35736367 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0003808 increased atrioventricular cushion size IAGP N RGD:5509061 20230601 MGI PMID:35736367 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0003923 abnormal heart left atrium morphology IAGP N RGD:5509061 20230601 MGI PMID:35736367 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:12756295 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:19897492 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220428 MGI PMID:29659998 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220428 MGI PMID:29659998 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0005243 hemothorax IAGP N RGD:5509061 20230601 MGI PMID:35736367 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220428 MGI PMID:29659998 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0008727 increased heart right atrium size IAGP N RGD:5509061 20230601 MGI PMID:35736367 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220428 MGI PMID:29659998 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20220428 MGI PMID:29659998 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20231221 MGI PMID:35736367 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220428 MGI PMID:29659998 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20230601 MGI PMID:35736367 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0010647 heart left atrium hypoplasia IAGP N RGD:5509061 20230601 MGI PMID:35736367 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12756295 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19897492 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12756295 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20230601 MGI PMID:35736367 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12756295 1314177 Carm1 coactivator-associated arginine methyltransferase 1 gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20141003 MGI PMID:19897492 1314179 Cmpk2 cytidine/uridine monophosphate kinase 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1314179 Cmpk2 cytidine/uridine monophosphate kinase 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 1314179 Cmpk2 cytidine/uridine monophosphate kinase 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20170105 MGI 1314179 Cmpk2 cytidine/uridine monophosphate kinase 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1314179 Cmpk2 cytidine/uridine monophosphate kinase 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20170105 MGI 1314181 Gpr107 G protein-coupled receptor 107 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160526 MGI PMID:24849652 1314181 Gpr107 G protein-coupled receptor 107 gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20160526 MGI PMID:24849652 1314181 Gpr107 G protein-coupled receptor 107 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160526 MGI PMID:24849652 1314181 Gpr107 G protein-coupled receptor 107 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314182 Pcnx2 pecanex homolog 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220811 MGI 1314182 Pcnx2 pecanex homolog 2 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1314182 Pcnx2 pecanex homolog 2 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20220811 MGI 1314182 Pcnx2 pecanex homolog 2 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20170202 MGI PMID:25010494 1314182 Pcnx2 pecanex homolog 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1314187 Sh3glb2 SH3-domain GRB2-like endophilin B2 gene MP:0004043 abnormal pH regulation IAGP N RGD:5509061 20230629 MGI PMID:28455444 1314187 Sh3glb2 SH3-domain GRB2-like endophilin B2 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20230629 MGI PMID:28455444 1314187 Sh3glb2 SH3-domain GRB2-like endophilin B2 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20230629 MGI PMID:28455444 1314187 Sh3glb2 SH3-domain GRB2-like endophilin B2 gene MP:0030951 abnormal endocytosis IAGP N RGD:5509061 20230629 MGI PMID:28455444 1314192 Polr3h polymerase (RNA) III (DNA directed) polypeptide H gene MP:0001921 reduced fertility IAGP N RGD:5509061 20210520 MGI PMID:30830215 1314192 Polr3h polymerase (RNA) III (DNA directed) polypeptide H gene MP:0001935 decreased litter size IAGP N RGD:5509061 20210520 MGI PMID:30830215 1314192 Polr3h polymerase (RNA) III (DNA directed) polypeptide H gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20210520 MGI PMID:30830215 1314192 Polr3h polymerase (RNA) III (DNA directed) polypeptide H gene MP:0008940 delayed balanopreputial separation IAGP N RGD:5509061 20210520 MGI PMID:30830215 1314192 Polr3h polymerase (RNA) III (DNA directed) polypeptide H gene MP:0009008 delayed estrous cycle IAGP N RGD:5509061 20210520 MGI PMID:30830215 1314192 Polr3h polymerase (RNA) III (DNA directed) polypeptide H gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20210520 MGI PMID:30830215 1314192 Polr3h polymerase (RNA) III (DNA directed) polypeptide H gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20210520 MGI PMID:30830215 1314192 Polr3h polymerase (RNA) III (DNA directed) polypeptide H gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20210520 MGI PMID:30830215 1314195 Spire1 spire type actin nucleation factor 1 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20151231 MGI PMID:24345451 1314195 Spire1 spire type actin nucleation factor 1 gene MP:0009455 enhanced cued conditioning behavior IAGP N RGD:5509061 20151231 MGI PMID:24345451 1314195 Spire1 spire type actin nucleation factor 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20151231 MGI PMID:24345451 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20150219 MGI PMID:15866165 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:22393260 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0000550 abnormal forelimb morphology IEA N RGD:5509061 20141003 MGI 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0000564 syndactyly IEA N RGD:5509061 20141003 MGI 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7870176 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:10090727 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0001304 cataract IEA N RGD:5509061 20141003 MGI 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:22393260 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0001677 absent apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:10090727 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:10090727 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:10090727 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7870176 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10090727 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10090727 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7870176 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10090727 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10489374 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20141003 MGI 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:15866165 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:15866165 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0005014 increased B cell number IEA N RGD:5509061 20141003 MGI 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:7870176 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:7870176 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0005316 abnormal response to tactile stimuli IEA N RGD:5509061 20141003 MGI 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:10090727 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0006302 abnormal ectomesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:10090727 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0006422 increased mammary adenoacanthoma incidence IAGP N RGD:5509061 20150219 MGI PMID:10489374 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22875805 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20141003 MGI 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22875805 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:7870176 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22875805 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0010318 increased salivary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10489374 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10090727 1314198 Tcf7 transcription factor 7, T cell specific gene MP:0013166 small forelimb buds IAGP N RGD:5509061 20141003 MGI PMID:10090727 1314199 Abca13 ATP-binding cassette, sub-family A member 13 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1314199 Abca13 ATP-binding cassette, sub-family A member 13 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20220901 MGI PMID:33478937 1314199 Abca13 ATP-binding cassette, sub-family A member 13 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20220901 MGI PMID:33478937 1314199 Abca13 ATP-binding cassette, sub-family A member 13 gene MP:0009198 abnormal male genitalia morphology IEA N RGD:5509061 20201231 MGI 1314199 Abca13 ATP-binding cassette, sub-family A member 13 gene MP:0021013 abnormal synaptic vesicle endocytosis IAGP N RGD:5509061 20220901 MGI PMID:33478937 1314207 Spart spartin gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1314207 Spart spartin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0003707 increased cell nucleus count IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22619377 1314207 Spart spartin gene MP:0010574 dilated aorta IEA N RGD:5509061 20230601 MGI 1314207 Spart spartin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1314207 Spart spartin gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1314210 Kat2b K(lysine) acetyltransferase 2B gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1314210 Kat2b K(lysine) acetyltransferase 2B gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:11017084 1314210 Kat2b K(lysine) acetyltransferase 2B gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11017084 1314210 Kat2b K(lysine) acetyltransferase 2B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11017084 1314210 Kat2b K(lysine) acetyltransferase 2B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11027331 1314210 Kat2b K(lysine) acetyltransferase 2B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11017084 1314210 Kat2b K(lysine) acetyltransferase 2B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11027331 1314210 Kat2b K(lysine) acetyltransferase 2B gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1314210 Kat2b K(lysine) acetyltransferase 2B gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1314210 Kat2b K(lysine) acetyltransferase 2B gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20181227 MGI 1314210 Kat2b K(lysine) acetyltransferase 2B gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1314210 Kat2b K(lysine) acetyltransferase 2B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11027331 1314210 Kat2b K(lysine) acetyltransferase 2B gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11017084 1314213 Epyc epiphycan gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160505 MGI PMID:19932218 1314213 Epyc epiphycan gene MP:0003109 short femur IAGP N RGD:5509061 20160505 MGI PMID:19932218 1314213 Epyc epiphycan gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20160505 MGI PMID:19932218 1314213 Epyc epiphycan gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20190530 MGI PMID:28864419 1314213 Epyc epiphycan gene MP:0013304 osteophytes IAGP N RGD:5509061 20160505 MGI PMID:19932218 1314213 Epyc epiphycan gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20160505 MGI PMID:19932218 1314217 Lats2 large tumor suppressor 2 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15343267 1314217 Lats2 large tumor suppressor 2 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15343267 1314217 Lats2 large tumor suppressor 2 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15343267 1314217 Lats2 large tumor suppressor 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15343267 1314217 Lats2 large tumor suppressor 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20150910 MGI PMID:26109051 1314217 Lats2 large tumor suppressor 2 gene MP:0000736 delayed muscle development IAGP N RGD:5509061 20141003 MGI PMID:17478426 1314217 Lats2 large tumor suppressor 2 gene MP:0000828 abnormal fourth ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17478426 1314217 Lats2 large tumor suppressor 2 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:15343267 1314217 Lats2 large tumor suppressor 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:17478426 1314217 Lats2 large tumor suppressor 2 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20111116 MGI 1314217 Lats2 large tumor suppressor 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17478426 1314217 Lats2 large tumor suppressor 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15343267 1314217 Lats2 large tumor suppressor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150910 MGI PMID:26109051 1314217 Lats2 large tumor suppressor 2 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:17478426 1314217 Lats2 large tumor suppressor 2 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:17478426 1314217 Lats2 large tumor suppressor 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20150910 MGI PMID:26109051 1314217 Lats2 large tumor suppressor 2 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:15343267 1314217 Lats2 large tumor suppressor 2 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:17478426 1314217 Lats2 large tumor suppressor 2 gene MP:0003707 increased cell nucleus count IAGP N RGD:5509061 20141003 MGI PMID:17478426 1314217 Lats2 large tumor suppressor 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15343267 1314217 Lats2 large tumor suppressor 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17478426 1314217 Lats2 large tumor suppressor 2 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:17478426 1314217 Lats2 large tumor suppressor 2 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:15343267 1314217 Lats2 large tumor suppressor 2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:17478426 1314217 Lats2 large tumor suppressor 2 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:15343267 1314217 Lats2 large tumor suppressor 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17478426 1314217 Lats2 large tumor suppressor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15343267 1314217 Lats2 large tumor suppressor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17478426 1314217 Lats2 large tumor suppressor 2 gene MP:0013182 increased spinal cord apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17478426 1314217 Lats2 large tumor suppressor 2 gene MP:0013611 abnormal bile duct epithelium morphology IAGP N RGD:5509061 20150910 MGI PMID:26109051 1314217 Lats2 large tumor suppressor 2 gene MP:0014239 abnormal intracellular organelle morphology IAGP N RGD:5509061 20230615 MGI PMID:17478426 1314217 Lats2 large tumor suppressor 2 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:23230145 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:16039642 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:16039642 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16039642 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:16039642 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0001241 absent epidermis stratum corneum IAGP N RGD:5509061 20141003 MGI PMID:16039642 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:16039642 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12773572 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:16039642 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:12773572 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:16039642 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:16039642 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:12773572 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12773572 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12773572 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:16039642 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12773572 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16039642 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12773572 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0011184 absent embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:12773572 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:12773572 1314219 Taf10 TATA-box binding protein associated factor 10 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:12773572 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20240111 MGI PMID:37459052 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20160602 MGI PMID:25948814 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20240111 MGI PMID:37459052 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20160602 MGI PMID:25948814 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20240111 MGI PMID:37459052 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20240111 MGI PMID:37459052 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0000692 small spleen IAGP N RGD:5509061 20160602 MGI PMID:25948814 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240111 MGI PMID:37459052 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0001505 hunched posture IAGP N RGD:5509061 20240111 MGI PMID:37459052 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20240111 MGI PMID:37459052 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0002816 colitis IAGP N RGD:5509061 20240111 MGI PMID:37459052 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20240111 MGI PMID:37459052 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20240111 MGI PMID:37459052 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20160602 MGI PMID:25948814 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20160602 MGI PMID:25948814 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20160602 MGI PMID:25948814 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20160602 MGI PMID:25948814 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20160602 MGI PMID:25948814 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20160602 MGI PMID:25948814 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20160602 MGI PMID:25948814 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20160602 MGI PMID:25948814 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20240111 MGI PMID:37459052 1314221 Tnfaip8 tumor necrosis factor, alpha-induced protein 8 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20240111 MGI PMID:37459052 1314223 Ndufb5 NADH:ubiquinone oxidoreductase subunit B5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1314223 Ndufb5 NADH:ubiquinone oxidoreductase subunit B5 gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20230601 MGI 1314223 Ndufb5 NADH:ubiquinone oxidoreductase subunit B5 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 1314223 Ndufb5 NADH:ubiquinone oxidoreductase subunit B5 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20230601 MGI 1314223 Ndufb5 NADH:ubiquinone oxidoreductase subunit B5 gene MP:0001726 abnormal allantois morphology IEA N RGD:5509061 20230601 MGI 1314223 Ndufb5 NADH:ubiquinone oxidoreductase subunit B5 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20230601 MGI 1314223 Ndufb5 NADH:ubiquinone oxidoreductase subunit B5 gene MP:0002861 abnormal tail bud morphology IEA N RGD:5509061 20230601 MGI 1314223 Ndufb5 NADH:ubiquinone oxidoreductase subunit B5 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20230601 MGI 1314223 Ndufb5 NADH:ubiquinone oxidoreductase subunit B5 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20230601 MGI 1314223 Ndufb5 NADH:ubiquinone oxidoreductase subunit B5 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20230601 MGI 1314223 Ndufb5 NADH:ubiquinone oxidoreductase subunit B5 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1314223 Ndufb5 NADH:ubiquinone oxidoreductase subunit B5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1314223 Ndufb5 NADH:ubiquinone oxidoreductase subunit B5 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20230601 MGI 1314225 Sorcs1 sortilin-related VPS10 domain containing receptor 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:20881129 1314227 Ap1s1 adaptor protein complex AP-1, sigma 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:18541143 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0001147 small testis IAGP N RGD:5509061 20220217 MGI PMID:24355749 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220217 MGI PMID:24355749 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220217 MGI PMID:24355749 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18541143 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220217 MGI PMID:24355749 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18541143 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18541143 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18541143 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220217 MGI PMID:24355749 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18541143 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20220217 MGI PMID:24355749 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20220217 MGI PMID:24355749 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:11287179 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220217 MGI PMID:24355749 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220217 MGI PMID:24355749 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220217 MGI PMID:24355749 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:11287179 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:11287179 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220217 MGI PMID:24355749 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20220217 MGI PMID:24355749 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18541143 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18541143 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11287179 1314229 Racgap1 Rac GTPase-activating protein 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220217 MGI PMID:24355749 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20210805 MGI PMID:34142127 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:22326607 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:22484060 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20180215 MGI PMID:25248974 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:22326607 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20180215 MGI PMID:25248974 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:22326607 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:15170214 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:22326607 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000585 kinked tail IAGP N RGD:5509061 20210805 MGI PMID:34142127 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:19956724 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:22326607 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0000592 short tail IAGP N RGD:5509061 20180215 MGI PMID:25248974 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0001258 decreased body length IAGP N RGD:5509061 20180215 MGI PMID:25248974 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:22326607 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20180215 MGI PMID:25248974 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:15170214 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20180215 MGI PMID:25248974 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19956724 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:22326607 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:19956724 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20180215 MGI PMID:25248974 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:19956724 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:22326607 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0004612 fusion of vertebral bodies IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0004645 decreased vertebrae number IAGP N RGD:5509061 20180215 MGI PMID:25248974 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:22326607 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20210805 MGI PMID:34142127 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0005224 abnormal left-right axis symmetry of the somites IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20180215 MGI PMID:25248974 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0005227 abnormal vertebral body development IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22326607 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19956724 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22326607 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19956724 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11641270 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:15170214 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0012669 abnormal somite segmentation clock IAGP N RGD:5509061 20180215 MGI PMID:25248974 1314232 Hes7 hes family bHLH transcription factor 7 gene MP:0012728 abnormal somite border morphology IAGP N RGD:5509061 20180215 MGI PMID:25248974 1314241 Pkn3 protein kinase N3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20151015 MGI PMID:25234167 1314241 Pkn3 protein kinase N3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20151015 MGI PMID:25234167 1314241 Pkn3 protein kinase N3 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20151015 MGI PMID:25234167 1314241 Pkn3 protein kinase N3 gene MP:0002083 premature death IAGP N RGD:5509061 20151015 MGI PMID:25234167 1314241 Pkn3 protein kinase N3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151015 MGI PMID:25234167 1314241 Pkn3 protein kinase N3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20171109 MGI PMID:26774483 1314241 Pkn3 protein kinase N3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 1314241 Pkn3 protein kinase N3 gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20151015 MGI PMID:25234167 1314241 Pkn3 protein kinase N3 gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20151015 MGI PMID:25234167 1314241 Pkn3 protein kinase N3 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1314243 Bfsp2 beaded filament structural protein 2, phakinin gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:12454043 1314243 Bfsp2 beaded filament structural protein 2, phakinin gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:12573667 1314243 Bfsp2 beaded filament structural protein 2, phakinin gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12573667 1314243 Bfsp2 beaded filament structural protein 2, phakinin gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:14667833 1314243 Bfsp2 beaded filament structural protein 2, phakinin gene MP:0003096 increased corneal light-scattering IAGP N RGD:5509061 20141003 MGI PMID:12573667 1314243 Bfsp2 beaded filament structural protein 2, phakinin gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20161013 MGI PMID:12573667 1314243 Bfsp2 beaded filament structural protein 2, phakinin gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20161013 MGI PMID:14667833 1314244 Zfp60 zinc finger protein 60 gene MP:0000745 tremors IEA N RGD:5509061 20201022 MGI 1314244 Zfp60 zinc finger protein 60 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1314244 Zfp60 zinc finger protein 60 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1314244 Zfp60 zinc finger protein 60 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210826 MGI 1314244 Zfp60 zinc finger protein 60 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:9553047 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12077323 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:9553047 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:14614148 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:14614148 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:9553047 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:9553047 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9553047 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9553047 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9553047 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:9553047 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:14614148 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14614148 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11940669 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12077323 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:14614148 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20643340 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9553047 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:14614148 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:9553047 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:9553047 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0008850 increased hemoglobin concentration distribution width IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0008850 increased hemoglobin concentration distribution width IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:20643340 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:14614148 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:14614148 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:14614148 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:14614148 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9553047 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14614148 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20010697 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19927129 1314246 Zfpm1 zinc finger protein, multitype 1 gene MP:0020431 decreased platelet alpha-granule number IAGP N RGD:5509061 20170720 MGI PMID:19927129 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:19099580 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:19099580 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:19099580 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20170921 MGI PMID:19099580 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19099580 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19099580 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19099580 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0003387 aorta coarctation IAGP N RGD:5509061 20141003 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:19099580 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0004418 small parietal bone IAGP N RGD:5509061 20141003 MGI PMID:19099580 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:19099580 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19099580 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160804 MGI 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160804 MGI 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0006411 upturned snout IAGP N RGD:5509061 20170921 MGI PMID:19099580 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0010563 increased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0013270 fourth pharyngeal arch hypoplasia IAGP N RGD:5509061 20171109 MGI PMID:19470456 1314249 Baz1b bromodomain adjacent to zinc finger domain, 1B gene MP:0030049 prominent forehead IAGP N RGD:5509061 20170921 MGI PMID:19099580 1314255 Abca9 ATP-binding cassette, sub-family A member 9 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1314261 Pnpla3 patatin-like phospholipase domain containing 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180927 MGI PMID:24917523 1314261 Pnpla3 patatin-like phospholipase domain containing 3 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20180927 MGI PMID:24917523 1314261 Pnpla3 patatin-like phospholipase domain containing 3 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20180927 MGI PMID:24917523 1314261 Pnpla3 patatin-like phospholipase domain containing 3 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180927 MGI PMID:24917523 1314264 Rimoc1 RAB7A interacting MON1-CCZ1 complex subunit 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20230720 MGI 1314264 Rimoc1 RAB7A interacting MON1-CCZ1 complex subunit 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20240523 MGI 1314264 Rimoc1 RAB7A interacting MON1-CCZ1 complex subunit 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20230720 MGI 1314264 Rimoc1 RAB7A interacting MON1-CCZ1 complex subunit 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20230720 MGI 1314264 Rimoc1 RAB7A interacting MON1-CCZ1 complex subunit 1 gene MP:0005533 increased body temperature IEA N RGD:5509061 20230720 MGI 1314264 Rimoc1 RAB7A interacting MON1-CCZ1 complex subunit 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230720 MGI 1314264 Rimoc1 RAB7A interacting MON1-CCZ1 complex subunit 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20230720 MGI 1314265 Fam227a family with sequence similarity 227, member A gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 1314268 Plcl2 phospholipase C-like 2 gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:14517301 1314268 Plcl2 phospholipase C-like 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:14517301 1314268 Plcl2 phospholipase C-like 2 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14517301 1314268 Plcl2 phospholipase C-like 2 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:14517301 1314268 Plcl2 phospholipase C-like 2 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14517301 1314268 Plcl2 phospholipase C-like 2 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:14517301 1314268 Plcl2 phospholipase C-like 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:14517301 1314268 Plcl2 phospholipase C-like 2 gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:14517301 1314270 Rai14 retinoic acid induced 14 gene MP:0001575 cyanosis IEA N RGD:5509061 20210520 MGI 1314270 Rai14 retinoic acid induced 14 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1314270 Rai14 retinoic acid induced 14 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1314270 Rai14 retinoic acid induced 14 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20181227 MGI 1314270 Rai14 retinoic acid induced 14 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1314270 Rai14 retinoic acid induced 14 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1314272 Ncf4 neutrophil cytosolic factor 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16880254 1314272 Ncf4 neutrophil cytosolic factor 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16990793 1314272 Ncf4 neutrophil cytosolic factor 4 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16880254 1314272 Ncf4 neutrophil cytosolic factor 4 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16990793 1314272 Ncf4 neutrophil cytosolic factor 4 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20181227 MGI 1314272 Ncf4 neutrophil cytosolic factor 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16990793 1314276 Slamf9 SLAM family member 9 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20191107 MGI PMID:31346085 1314276 Slamf9 SLAM family member 9 gene MP:0008524 increased plasmacytoid dendritic cell number IAGP N RGD:5509061 20191107 MGI PMID:31346085 1314276 Slamf9 SLAM family member 9 gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20191107 MGI PMID:31346085 1314278 Efna2 ephrin A2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20170209 MGI PMID:15713841 1314278 Efna2 ephrin A2 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20170209 MGI PMID:16025107 1314278 Efna2 ephrin A2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20170209 MGI PMID:10774725 1314278 Efna2 ephrin A2 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20170209 MGI PMID:25281279 1314278 Efna2 ephrin A2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20170209 MGI PMID:25281279 1314278 Efna2 ephrin A2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1314278 Efna2 ephrin A2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20170209 MGI PMID:25281279 1314278 Efna2 ephrin A2 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20170209 MGI PMID:25281279 1314278 Efna2 ephrin A2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20170209 MGI PMID:25281279 1314278 Efna2 ephrin A2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20170209 MGI PMID:25281279 1314278 Efna2 ephrin A2 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20170209 MGI PMID:25281279 1314278 Efna2 ephrin A2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20170209 MGI PMID:15713841 1314278 Efna2 ephrin A2 gene MP:0002634 abnormal sensorimotor gating IAGP N RGD:5509061 20170209 MGI PMID:25281279 1314278 Efna2 ephrin A2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20170209 MGI PMID:25281279 1314278 Efna2 ephrin A2 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20170209 MGI PMID:25281279 1314278 Efna2 ephrin A2 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20170209 MGI PMID:25281279 1314278 Efna2 ephrin A2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20170209 MGI PMID:15713841 1314280 Ift57 intraflagellar transport 57 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0004203 abnormal cranial flexure morphology IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314280 Ift57 intraflagellar transport 57 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17027958 1314282 Sec61a2 SEC61 translocon subunit alpha 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 1314282 Sec61a2 SEC61 translocon subunit alpha 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1314282 Sec61a2 SEC61 translocon subunit alpha 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11909824 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0001413 abnormal response to new environment IEA N RGD:5509061 20141003 MGI 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11909824 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16380103 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20151112 MGI PMID:26241864 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15249187 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19590044 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20171005 MGI PMID:22465693 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:11909824 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15059932 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:22829020 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15059932 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:15059932 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19590044 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002833 increased heart weight IAGP N RGD:5509061 20151112 MGI PMID:26241864 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15059932 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16380103 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20160804 MGI 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22829020 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:15249187 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19590044 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:22829020 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0004058 abnormal ventricle papillary muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0004063 dilated heart left atrium IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:15059932 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20171005 MGI PMID:22465693 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0004094 abnormal M line morphology IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:14500336 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20171005 MGI PMID:22465693 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:22829020 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:19590044 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:22829020 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20151112 MGI PMID:26241864 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11909824 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15249187 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19590044 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20171005 MGI PMID:22465693 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:11909824 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22829020 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15059932 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11909824 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15249187 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19590044 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22829020 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20151112 MGI PMID:26241864 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20141003 MGI 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20151112 MGI PMID:26241864 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20171005 MGI PMID:22465693 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:15059932 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:26241864 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:11909824 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:22829020 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:10545522 1314285 Mybpc3 myosin binding protein C, cardiac gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:11909824 1314292 Pop4 processing of precursor 4, ribonuclease P/MRP family, (S. cerevisiae) gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20160107 MGI 1314292 Pop4 processing of precursor 4, ribonuclease P/MRP family, (S. cerevisiae) gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20201231 MGI 1314292 Pop4 processing of precursor 4, ribonuclease P/MRP family, (S. cerevisiae) gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20160107 MGI 1314292 Pop4 processing of precursor 4, ribonuclease P/MRP family, (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314294 Tdrd6 tudor domain containing 6 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19345099 1314294 Tdrd6 tudor domain containing 6 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19345099 1314294 Tdrd6 tudor domain containing 6 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19345099 1314294 Tdrd6 tudor domain containing 6 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21670278 1314294 Tdrd6 tudor domain containing 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19345099 1314294 Tdrd6 tudor domain containing 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21670278 1314294 Tdrd6 tudor domain containing 6 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:19345099 1314294 Tdrd6 tudor domain containing 6 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:19345099 1314295 Tnk2 tyrosine kinase, non-receptor, 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1314296 Mtmr10 myotubularin related protein 10 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20210121 MGI PMID:32876667 1314296 Mtmr10 myotubularin related protein 10 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1314297 Mesp2 mesoderm posterior 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16996494 1314297 Mesp2 mesoderm posterior 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18849530 1314297 Mesp2 mesoderm posterior 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:21098559 1314297 Mesp2 mesoderm posterior 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:22484060 1314297 Mesp2 mesoderm posterior 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:16996494 1314297 Mesp2 mesoderm posterior 2 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20171102 MGI PMID:9739106 1314297 Mesp2 mesoderm posterior 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:11973278 1314297 Mesp2 mesoderm posterior 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:16996494 1314297 Mesp2 mesoderm posterior 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:18849530 1314297 Mesp2 mesoderm posterior 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:21098559 1314297 Mesp2 mesoderm posterior 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20171102 MGI PMID:9739106 1314297 Mesp2 mesoderm posterior 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:10887078 1314297 Mesp2 mesoderm posterior 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:11973278 1314297 Mesp2 mesoderm posterior 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:21098559 1314297 Mesp2 mesoderm posterior 2 gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:16996494 1314297 Mesp2 mesoderm posterior 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:21098559 1314297 Mesp2 mesoderm posterior 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9739106 1314297 Mesp2 mesoderm posterior 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10887078 1314297 Mesp2 mesoderm posterior 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:10887078 1314297 Mesp2 mesoderm posterior 2 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:10887078 1314297 Mesp2 mesoderm posterior 2 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:10887078 1314297 Mesp2 mesoderm posterior 2 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10887078 1314297 Mesp2 mesoderm posterior 2 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:10887078 1314297 Mesp2 mesoderm posterior 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:10932180 1314297 Mesp2 mesoderm posterior 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:11973278 1314297 Mesp2 mesoderm posterior 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16996494 1314297 Mesp2 mesoderm posterior 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:17306789 1314297 Mesp2 mesoderm posterior 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:20335362 1314297 Mesp2 mesoderm posterior 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:21098559 1314297 Mesp2 mesoderm posterior 2 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:17306789 1314297 Mesp2 mesoderm posterior 2 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:15677726 1314297 Mesp2 mesoderm posterior 2 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:10887078 1314297 Mesp2 mesoderm posterior 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10887078 1314297 Mesp2 mesoderm posterior 2 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18849530 1314297 Mesp2 mesoderm posterior 2 gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:10887078 1314297 Mesp2 mesoderm posterior 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20171102 MGI PMID:9739106 1314297 Mesp2 mesoderm posterior 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18849530 1314297 Mesp2 mesoderm posterior 2 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:10887078 1314297 Mesp2 mesoderm posterior 2 gene MP:0002632 vestigial tail IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16996494 1314297 Mesp2 mesoderm posterior 2 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16996494 1314297 Mesp2 mesoderm posterior 2 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16996494 1314297 Mesp2 mesoderm posterior 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0003794 delayed somite formation IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:10932180 1314297 Mesp2 mesoderm posterior 2 gene MP:0004600 abnormal vertebral transverse process morphology IAGP N RGD:5509061 20141003 MGI PMID:10932180 1314297 Mesp2 mesoderm posterior 2 gene MP:0004604 abnormal vertebral pedicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10932180 1314297 Mesp2 mesoderm posterior 2 gene MP:0004605 abnormal vertebral lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:10932180 1314297 Mesp2 mesoderm posterior 2 gene MP:0004605 abnormal vertebral lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:11973278 1314297 Mesp2 mesoderm posterior 2 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:16996494 1314297 Mesp2 mesoderm posterior 2 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:21098559 1314297 Mesp2 mesoderm posterior 2 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:16996494 1314297 Mesp2 mesoderm posterior 2 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:21098559 1314297 Mesp2 mesoderm posterior 2 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:18849530 1314297 Mesp2 mesoderm posterior 2 gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:20335362 1314297 Mesp2 mesoderm posterior 2 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:16996494 1314297 Mesp2 mesoderm posterior 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18849530 1314297 Mesp2 mesoderm posterior 2 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:10887078 1314297 Mesp2 mesoderm posterior 2 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:11973278 1314297 Mesp2 mesoderm posterior 2 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:11973278 1314297 Mesp2 mesoderm posterior 2 gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:21098559 1314297 Mesp2 mesoderm posterior 2 gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11973278 1314297 Mesp2 mesoderm posterior 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314297 Mesp2 mesoderm posterior 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10887078 1314297 Mesp2 mesoderm posterior 2 gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:10887078 1314297 Mesp2 mesoderm posterior 2 gene MP:0012184 absent paraxial mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10887078 1314297 Mesp2 mesoderm posterior 2 gene MP:0012728 abnormal somite border morphology IAGP N RGD:5509061 20141003 MGI PMID:11973278 1314297 Mesp2 mesoderm posterior 2 gene MP:0012728 abnormal somite border morphology IAGP N RGD:5509061 20141003 MGI PMID:17306789 1314297 Mesp2 mesoderm posterior 2 gene MP:0012728 abnormal somite border morphology IAGP N RGD:5509061 20141003 MGI PMID:9242490 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0000160 kyphosis IAGP N RGD:5509061 20180927 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0000746 weakness IAGP N RGD:5509061 20180927 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180927 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20180927 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:23372768 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:23372768 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:23372768 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:23372768 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0001705 abnormal proximal-distal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:23372768 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0001717 absent ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:23372768 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:23372768 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0002583 absent extraembryonic ectoderm IAGP N RGD:5509061 20141003 MGI PMID:23372768 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23372768 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20180927 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:23372768 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:23372768 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0005150 cachexia IAGP N RGD:5509061 20180927 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200402 MGI 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20180927 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20180927 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20180927 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20180927 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20180927 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:23372768 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20180927 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23372768 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:23372768 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20180927 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20180927 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20180927 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0014342 abnormal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:29898916 1314305 Atad3a ATPase family, AAA domain containing 3A gene MP:0014389 decreased skeletal muscle fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:29898916 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:12808099 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:12808099 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16525419 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18093944 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18093944 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18093944 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:12808099 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0001876 decreased inflammatory response IEA N RGD:5509061 20220811 MGI 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12808099 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12808099 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12808099 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12808099 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12808099 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:18093944 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:16525419 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:18093944 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0003880 abnormal central pattern generator function IAGP N RGD:5509061 20141003 MGI PMID:18093944 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0004557 dilated allantois IAGP N RGD:5509061 20141003 MGI PMID:12808099 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0004712 notochord degeneration IAGP N RGD:5509061 20141003 MGI PMID:12808099 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16525419 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16525419 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16525419 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12808099 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:16525419 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:16525419 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0008503 abnormal spinal cord grey matter morphology IAGP N RGD:5509061 20141003 MGI PMID:18093944 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12808099 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:18093944 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18093944 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808099 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:16525419 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0011856 abnormal glomerular filtration barrier function IAGP N RGD:5509061 20141003 MGI PMID:16525419 1314307 Nck2 non-catalytic region of tyrosine kinase adaptor protein 2 gene MP:0020100 decreased susceptibility to diet-induced aortic fatty streak lesions IEA N RGD:5509061 20220811 MGI 1314309 Klf16 Kruppel-like transcription factor 16 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1314309 Klf16 Kruppel-like transcription factor 16 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1314309 Klf16 Kruppel-like transcription factor 16 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 1314309 Klf16 Kruppel-like transcription factor 16 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1314309 Klf16 Kruppel-like transcription factor 16 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1314309 Klf16 Kruppel-like transcription factor 16 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1314309 Klf16 Kruppel-like transcription factor 16 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1314309 Klf16 Kruppel-like transcription factor 16 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1314309 Klf16 Kruppel-like transcription factor 16 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1314309 Klf16 Kruppel-like transcription factor 16 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20211021 MGI 1314309 Klf16 Kruppel-like transcription factor 16 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1314311 Cux2 cut-like homeobox 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18223201 1314311 Cux2 cut-like homeobox 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20230413 MGI PMID:35379703 1314311 Cux2 cut-like homeobox 2 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20230413 MGI PMID:35379703 1314311 Cux2 cut-like homeobox 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18033766 1314311 Cux2 cut-like homeobox 2 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:18033766 1314311 Cux2 cut-like homeobox 2 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20230413 MGI PMID:35379703 1314311 Cux2 cut-like homeobox 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18223201 1314311 Cux2 cut-like homeobox 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18223201 1314311 Cux2 cut-like homeobox 2 gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:19542352 1314311 Cux2 cut-like homeobox 2 gene MP:0004100 abnormal spinal cord interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19542352 1314311 Cux2 cut-like homeobox 2 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:18033766 1314311 Cux2 cut-like homeobox 2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:18033766 1314311 Cux2 cut-like homeobox 2 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:18033766 1314311 Cux2 cut-like homeobox 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:21315259 1314311 Cux2 cut-like homeobox 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20230413 MGI PMID:35379703 1314311 Cux2 cut-like homeobox 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20230413 MGI PMID:35379703 1314311 Cux2 cut-like homeobox 2 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20230413 MGI PMID:35379703 1314311 Cux2 cut-like homeobox 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20230413 MGI PMID:35379703 1314311 Cux2 cut-like homeobox 2 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18033766 1314311 Cux2 cut-like homeobox 2 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21315259 1314311 Cux2 cut-like homeobox 2 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:18033766 1314311 Cux2 cut-like homeobox 2 gene MP:0009689 abnormal neural tube ventricular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19542352 1314311 Cux2 cut-like homeobox 2 gene MP:0009691 abnormal neural tube marginal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18223201 1314311 Cux2 cut-like homeobox 2 gene MP:0009691 abnormal neural tube marginal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19542352 1314311 Cux2 cut-like homeobox 2 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20230413 MGI PMID:35379703 1314311 Cux2 cut-like homeobox 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18223201 1314311 Cux2 cut-like homeobox 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18033766 1314311 Cux2 cut-like homeobox 2 gene MP:0020337 abnormal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20230413 MGI PMID:35379703 1314311 Cux2 cut-like homeobox 2 gene MP:0021090 abnormal dendrite arborization pattern IAGP N RGD:5509061 20230413 MGI PMID:35379703 1314315 Vps4b vacuolar protein sorting 4B gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20201015 MGI PMID:26720614 1314315 Vps4b vacuolar protein sorting 4B gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20210506 MGI PMID:33682352 1314315 Vps4b vacuolar protein sorting 4B gene MP:0001714 absent trophoblast giant cells IAGP N RGD:5509061 20210506 MGI PMID:33682352 1314315 Vps4b vacuolar protein sorting 4B gene MP:0001914 hemorrhage IAGP N RGD:5509061 20210506 MGI PMID:33682352 1314315 Vps4b vacuolar protein sorting 4B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210506 MGI PMID:33682352 1314315 Vps4b vacuolar protein sorting 4B gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20210506 MGI PMID:33682352 1314315 Vps4b vacuolar protein sorting 4B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20210506 MGI PMID:33682352 1314315 Vps4b vacuolar protein sorting 4B gene MP:0004259 small placenta IAGP N RGD:5509061 20210506 MGI PMID:33682352 1314315 Vps4b vacuolar protein sorting 4B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20210506 MGI PMID:33682352 1314315 Vps4b vacuolar protein sorting 4B gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20210506 MGI PMID:33682352 1314317 Cd68 CD68 antigen gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:21991369 1314317 Cd68 CD68 antigen gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21991369 1314317 Cd68 CD68 antigen gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20231207 MGI 1314317 Cd68 CD68 antigen gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:21991369 1314317 Cd68 CD68 antigen gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:21572087 1314317 Cd68 CD68 antigen gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:21991369 1314317 Cd68 CD68 antigen gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:21991369 1314317 Cd68 CD68 antigen gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:21991369 1314317 Cd68 CD68 antigen gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:21991369 1314317 Cd68 CD68 antigen gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1314317 Cd68 CD68 antigen gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:21991369 1314319 Lsm3 LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated gene MP:0008573 increased circulating interferon-alpha level IAGP N RGD:5509061 20180830 MGI PMID:29706547 1314319 Lsm3 LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20180830 MGI PMID:29706547 1314319 Lsm3 LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20180830 MGI PMID:29706547 1314319 Lsm3 LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:29706547 1314319 Lsm3 LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated gene MP:0020947 decreased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:29706547 1314319 Lsm3 LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated gene MP:0031023 decreased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:29706547 1314322 Sectm1a secreted and transmembrane 1A gene MP:0001853 heart inflammation IAGP N RGD:5509061 20220127 MGI PMID:32170929 1314322 Sectm1a secreted and transmembrane 1A gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20220127 MGI PMID:32170929 1314322 Sectm1a secreted and transmembrane 1A gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20220127 MGI PMID:32170929 1314322 Sectm1a secreted and transmembrane 1A gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20220127 MGI PMID:32170929 1314322 Sectm1a secreted and transmembrane 1A gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20220127 MGI PMID:32170929 1314322 Sectm1a secreted and transmembrane 1A gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20220127 MGI PMID:32170929 1314322 Sectm1a secreted and transmembrane 1A gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20220127 MGI PMID:32170929 1314322 Sectm1a secreted and transmembrane 1A gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20220127 MGI PMID:32170929 1314322 Sectm1a secreted and transmembrane 1A gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20220127 MGI PMID:32170929 1314325 Efr3a EFR3 homolog A gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20190919 MGI PMID:28193719 1314325 Efr3a EFR3 homolog A gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20190919 MGI PMID:28193719 1314327 Thbs3 thrombospondin 3 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:15964815 1314327 Thbs3 thrombospondin 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15964815 1314327 Thbs3 thrombospondin 3 gene MP:0003416 premature bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15964815 1314329 Glipr1 GLI pathogenesis related 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18199537 1314329 Glipr1 GLI pathogenesis related 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230601 MGI 1314329 Glipr1 GLI pathogenesis related 1 gene MP:0008403 decreased cellular sensitivity to alkylating agents IAGP N RGD:5509061 20150212 MGI PMID:18199537 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:12644183 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:1339316 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:5556347 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:9071596 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:9475750 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000018 small ears IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000019 thick ears IEA N RGD:5509061 20111116 MGI 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000022 abnormal ear shape IEA N RGD:5509061 20111116 MGI 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000024 lowered ear position IEA N RGD:5509061 20111116 MGI 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20111116 MGI 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000088 short mandible IAGP N RGD:5509061 20151112 MGI PMID:26234751 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000097 short maxilla IEA N RGD:5509061 20111116 MGI 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9664685 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:1339316 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:9664685 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:13563786 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000445 short snout IAGP N RGD:5509061 20151112 MGI PMID:26234751 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000592 short tail IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0001394 circling IEA N RGD:5509061 20111116 MGI 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:5021246 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:5021246 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9664685 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9664685 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12644183 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20111116 MGI 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0002177 abnormal outer ear morphology IEA N RGD:5509061 20111116 MGI 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0002233 abnormal nose morphology IEA N RGD:5509061 20111116 MGI 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0002249 abnormal larynx morphology IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0002256 abnormal laryngeal cartilage morphology IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20190523 MGI PMID:20284341 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0003230 abnormal umbilical artery morphology IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:1339316 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20190523 MGI PMID:20284341 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0003585 large ureter IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0004350 long humerus IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0004357 long tibia IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0004359 short ulna IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0004360 absent ulna IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:9664685 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0004680 small xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:9664685 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0004695 increased length of long bones IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0004880 lung cyst IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0005352 small cranium IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:1339316 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0006325 impaired hearing IEA N RGD:5509061 20111116 MGI 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0008150 decreased diameter of long bones IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0008150 decreased diameter of long bones IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0008154 decreased diameter of humerus IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:13563786 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:9664685 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0008525 decreased cranium height IEA N RGD:5509061 20111116 MGI 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0009005 abnormal sesamoid bone of gastrocnemius morphology IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:5021246 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0010031 abnormal cranium size IAGP N RGD:5509061 20151112 MGI PMID:26234751 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0010113 abnormal sacrum morphology IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20151112 MGI PMID:26234751 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0010146 umbilical hernia IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:5021246 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0010770 preweaning lethality IEA N RGD:5509061 20111229 MGI 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1339316 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:5556347 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:5021246 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:5980120 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0011318 abnormal right renal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0011727 ectopic ovary IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0011835 abnormal urogenital fold morphology IAGP N RGD:5509061 20141003 MGI PMID:5692092 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20151112 MGI PMID:26234751 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0011872 absent xiphoid process IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0013618 decreased areal bone mineral density IAGP N RGD:5509061 20151112 MGI PMID:26234751 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0020084 short ears IAGP N RGD:5509061 20151112 MGI PMID:26234751 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0020084 short ears IAGP N RGD:5509061 20170914 MGI PMID:1339316 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0020084 short ears IAGP N RGD:5509061 20170914 MGI PMID:5556347 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0020084 short ears IAGP N RGD:5509061 20180315 MGI PMID:7710253 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0030422 abnormal outer ear cartilage morphology IEA N RGD:5509061 20171214 MGI 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0030867 small thyroid cartilage IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0030872 small cricoid cartilage IAGP N RGD:5509061 20230601 MGI PMID:24539717 1314331 Bmp5 bone morphogenetic protein 5 gene MP:0031286 unilateral cryptorchism IAGP N RGD:5509061 20211014 MGI PMID:5692092 1314333 Mbd1 methyl-CpG binding domain protein 1 gene MP:0000162 lordosis IEA N RGD:5509061 20181227 MGI 1314333 Mbd1 methyl-CpG binding domain protein 1 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:12748381 1314333 Mbd1 methyl-CpG binding domain protein 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:12748381 1314333 Mbd1 methyl-CpG binding domain protein 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12748381 1314333 Mbd1 methyl-CpG binding domain protein 1 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1314333 Mbd1 methyl-CpG binding domain protein 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:12748381 1314333 Mbd1 methyl-CpG binding domain protein 1 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12748381 1314333 Mbd1 methyl-CpG binding domain protein 1 gene MP:0003036 vertebral transformation IEA N RGD:5509061 20181227 MGI 1314333 Mbd1 methyl-CpG binding domain protein 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:12748381 1314333 Mbd1 methyl-CpG binding domain protein 1 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:12748381 1314333 Mbd1 methyl-CpG binding domain protein 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1314333 Mbd1 methyl-CpG binding domain protein 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:12748381 1314333 Mbd1 methyl-CpG binding domain protein 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:12748381 1314336 Ciao3 cytosolic iron-sulfur assembly component 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21367862 1314336 Ciao3 cytosolic iron-sulfur assembly component 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21367862 1314336 Ciao3 cytosolic iron-sulfur assembly component 3 gene MP:0006205 embryonic lethality between implantation and somite formation IEA N RGD:5509061 20141003 MGI 1314336 Ciao3 cytosolic iron-sulfur assembly component 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21367862 1314336 Ciao3 cytosolic iron-sulfur assembly component 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21367862 1314338 Pttg1ip pituitary tumor-transforming 1 interacting protein gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 1314338 Pttg1ip pituitary tumor-transforming 1 interacting protein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1314338 Pttg1ip pituitary tumor-transforming 1 interacting protein gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20200402 MGI 1314338 Pttg1ip pituitary tumor-transforming 1 interacting protein gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1314338 Pttg1ip pituitary tumor-transforming 1 interacting protein gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 1314338 Pttg1ip pituitary tumor-transforming 1 interacting protein gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1314342 Suds3 suppressor of defective silencing 3 homolog (S. cerevisiae) gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16767157 1314342 Suds3 suppressor of defective silencing 3 homolog (S. cerevisiae) gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16767157 1314342 Suds3 suppressor of defective silencing 3 homolog (S. cerevisiae) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16767157 1314342 Suds3 suppressor of defective silencing 3 homolog (S. cerevisiae) gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:14522945 1314342 Suds3 suppressor of defective silencing 3 homolog (S. cerevisiae) gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:14522945 1314342 Suds3 suppressor of defective silencing 3 homolog (S. cerevisiae) gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:14522945 1314342 Suds3 suppressor of defective silencing 3 homolog (S. cerevisiae) gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:16767157 1314342 Suds3 suppressor of defective silencing 3 homolog (S. cerevisiae) gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:14522945 1314342 Suds3 suppressor of defective silencing 3 homolog (S. cerevisiae) gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:16767157 1314342 Suds3 suppressor of defective silencing 3 homolog (S. cerevisiae) gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14522945 1314348 Dusp15 dual specificity phosphatase-like 15 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1314348 Dusp15 dual specificity phosphatase-like 15 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1314350 Procr protein C receptor, endothelial gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20160922 MGI PMID:26045607 1314350 Procr protein C receptor, endothelial gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20160922 MGI PMID:26045607 1314350 Procr protein C receptor, endothelial gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160922 MGI PMID:26045607 1314350 Procr protein C receptor, endothelial gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12218060 1314350 Procr protein C receptor, endothelial gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12218060 1314350 Procr protein C receptor, endothelial gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12218060 1314350 Procr protein C receptor, endothelial gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12353077 1314350 Procr protein C receptor, endothelial gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:15956290 1314350 Procr protein C receptor, endothelial gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:12218060 1314350 Procr protein C receptor, endothelial gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:17023579 1314350 Procr protein C receptor, endothelial gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:15956290 1314350 Procr protein C receptor, endothelial gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17023579 1314350 Procr protein C receptor, endothelial gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20160922 MGI PMID:26045607 1314350 Procr protein C receptor, endothelial gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12218060 1314350 Procr protein C receptor, endothelial gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20160922 MGI PMID:26045607 1314350 Procr protein C receptor, endothelial gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20160922 MGI PMID:26045607 1314350 Procr protein C receptor, endothelial gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20160922 MGI PMID:26045607 1314350 Procr protein C receptor, endothelial gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20160922 MGI PMID:26045607 1314350 Procr protein C receptor, endothelial gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20160922 MGI PMID:26045607 1314350 Procr protein C receptor, endothelial gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20160922 MGI PMID:26045607 1314350 Procr protein C receptor, endothelial gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15956290 1314350 Procr protein C receptor, endothelial gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17023579 1314350 Procr protein C receptor, endothelial gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12218060 1314350 Procr protein C receptor, endothelial gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15956290 1314350 Procr protein C receptor, endothelial gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160128 MGI PMID:25327250 1314350 Procr protein C receptor, endothelial gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15956290 1314350 Procr protein C receptor, endothelial gene MP:0012330 decreased circulating fibrinogen level IAGP N RGD:5509061 20200618 MGI PMID:15956290 1314350 Procr protein C receptor, endothelial gene MP:0013776 bone marrow failure IAGP N RGD:5509061 20160922 MGI PMID:26045607 1314350 Procr protein C receptor, endothelial gene MP:0020407 abnormal placental thrombosis IAGP N RGD:5509061 20161124 MGI PMID:12218060 1314350 Procr protein C receptor, endothelial gene MP:0031059 increased circulating C-reactive protein level IAGP N RGD:5509061 20200618 MGI PMID:15956290 1314350 Procr protein C receptor, endothelial gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:26045607 1314353 Trim46 tripartite motif-containing 46 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1314353 Trim46 tripartite motif-containing 46 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1314353 Trim46 tripartite motif-containing 46 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1314353 Trim46 tripartite motif-containing 46 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20220519 MGI 1314353 Trim46 tripartite motif-containing 46 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220519 MGI 1314355 Nodal nodal growth differentiation factor gene MP:0000087 absent mandible IAGP N RGD:5509061 20171026 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12231623 1314355 Nodal nodal growth differentiation factor gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12842913 1314355 Nodal nodal growth differentiation factor gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:12842913 1314355 Nodal nodal growth differentiation factor gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:21089073 1314355 Nodal nodal growth differentiation factor gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:9655392 1314355 Nodal nodal growth differentiation factor gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:15454269 1314355 Nodal nodal growth differentiation factor gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:18773491 1314355 Nodal nodal growth differentiation factor gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:12842913 1314355 Nodal nodal growth differentiation factor gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15454269 1314355 Nodal nodal growth differentiation factor gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:9655392 1314355 Nodal nodal growth differentiation factor gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:10452853 1314355 Nodal nodal growth differentiation factor gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:20730911 1314355 Nodal nodal growth differentiation factor gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:12842913 1314355 Nodal nodal growth differentiation factor gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0000508 right-sided isomerism IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0000508 right-sided isomerism IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:12231623 1314355 Nodal nodal growth differentiation factor gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:15454269 1314355 Nodal nodal growth differentiation factor gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:18773491 1314355 Nodal nodal growth differentiation factor gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:9655392 1314355 Nodal nodal growth differentiation factor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:18773491 1314355 Nodal nodal growth differentiation factor gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:12231623 1314355 Nodal nodal growth differentiation factor gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:18773491 1314355 Nodal nodal growth differentiation factor gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20160929 MGI PMID:22383895 1314355 Nodal nodal growth differentiation factor gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1314355 Nodal nodal growth differentiation factor gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1314355 Nodal nodal growth differentiation factor gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1314355 Nodal nodal growth differentiation factor gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:10518210 1314355 Nodal nodal growth differentiation factor gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:12431380 1314355 Nodal nodal growth differentiation factor gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:15302604 1314355 Nodal nodal growth differentiation factor gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:7924997 1314355 Nodal nodal growth differentiation factor gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20190228 MGI PMID:8429908 1314355 Nodal nodal growth differentiation factor gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:15302604 1314355 Nodal nodal growth differentiation factor gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:7924997 1314355 Nodal nodal growth differentiation factor gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:10452853 1314355 Nodal nodal growth differentiation factor gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:12471260 1314355 Nodal nodal growth differentiation factor gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:9655392 1314355 Nodal nodal growth differentiation factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:1879365 1314355 Nodal nodal growth differentiation factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8610012 1314355 Nodal nodal growth differentiation factor gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0001705 abnormal proximal-distal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15302604 1314355 Nodal nodal growth differentiation factor gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:18773491 1314355 Nodal nodal growth differentiation factor gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:20040491 1314355 Nodal nodal growth differentiation factor gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9655392 1314355 Nodal nodal growth differentiation factor gene MP:0001710 absent amniotic folds IAGP N RGD:5509061 20141003 MGI PMID:7924997 1314355 Nodal nodal growth differentiation factor gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:15302604 1314355 Nodal nodal growth differentiation factor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16950123 1314355 Nodal nodal growth differentiation factor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:7924997 1314355 Nodal nodal growth differentiation factor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:8610012 1314355 Nodal nodal growth differentiation factor gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:12842913 1314355 Nodal nodal growth differentiation factor gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12431380 1314355 Nodal nodal growth differentiation factor gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:15302604 1314355 Nodal nodal growth differentiation factor gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:1879365 1314355 Nodal nodal growth differentiation factor gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:8610012 1314355 Nodal nodal growth differentiation factor gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1314355 Nodal nodal growth differentiation factor gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:1879365 1314355 Nodal nodal growth differentiation factor gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:20508035 1314355 Nodal nodal growth differentiation factor gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7924997 1314355 Nodal nodal growth differentiation factor gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8610012 1314355 Nodal nodal growth differentiation factor gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7924997 1314355 Nodal nodal growth differentiation factor gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8610012 1314355 Nodal nodal growth differentiation factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12231623 1314355 Nodal nodal growth differentiation factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15454269 1314355 Nodal nodal growth differentiation factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15736223 1314355 Nodal nodal growth differentiation factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18773491 1314355 Nodal nodal growth differentiation factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8610012 1314355 Nodal nodal growth differentiation factor gene MP:0002174 abnormal gastrulation movements IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:12471260 1314355 Nodal nodal growth differentiation factor gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:16950123 1314355 Nodal nodal growth differentiation factor gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:1879365 1314355 Nodal nodal growth differentiation factor gene MP:0002767 situs ambiguus IAGP N RGD:5509061 20141003 MGI PMID:12231623 1314355 Nodal nodal growth differentiation factor gene MP:0002767 situs ambiguus IAGP N RGD:5509061 20141003 MGI PMID:8610012 1314355 Nodal nodal growth differentiation factor gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0002844 aortic hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:1879365 1314355 Nodal nodal growth differentiation factor gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20160929 MGI PMID:22383895 1314355 Nodal nodal growth differentiation factor gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:11456449 1314355 Nodal nodal growth differentiation factor gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1314355 Nodal nodal growth differentiation factor gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:12842913 1314355 Nodal nodal growth differentiation factor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160929 MGI PMID:22383895 1314355 Nodal nodal growth differentiation factor gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:15454269 1314355 Nodal nodal growth differentiation factor gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:12231623 1314355 Nodal nodal growth differentiation factor gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:18773491 1314355 Nodal nodal growth differentiation factor gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:9655392 1314355 Nodal nodal growth differentiation factor gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:12231623 1314355 Nodal nodal growth differentiation factor gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:8610012 1314355 Nodal nodal growth differentiation factor gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:8610012 1314355 Nodal nodal growth differentiation factor gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9655392 1314355 Nodal nodal growth differentiation factor gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:12231623 1314355 Nodal nodal growth differentiation factor gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:15454269 1314355 Nodal nodal growth differentiation factor gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:15466485 1314355 Nodal nodal growth differentiation factor gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:18773491 1314355 Nodal nodal growth differentiation factor gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:20508035 1314355 Nodal nodal growth differentiation factor gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11456449 1314355 Nodal nodal growth differentiation factor gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12842913 1314355 Nodal nodal growth differentiation factor gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20160929 MGI PMID:22383895 1314355 Nodal nodal growth differentiation factor gene MP:0004387 abnormal prechordal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0004387 abnormal prechordal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20508035 1314355 Nodal nodal growth differentiation factor gene MP:0004388 absent prechordal plate IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0004388 absent prechordal plate IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0004714 truncated notochord IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0004714 truncated notochord IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:1879365 1314355 Nodal nodal growth differentiation factor gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:20508035 1314355 Nodal nodal growth differentiation factor gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20160929 MGI PMID:22383895 1314355 Nodal nodal growth differentiation factor gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:10452853 1314355 Nodal nodal growth differentiation factor gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:9655392 1314355 Nodal nodal growth differentiation factor gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1314355 Nodal nodal growth differentiation factor gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0005542 cornea vascularization IEA N RGD:5509061 20201231 MGI 1314355 Nodal nodal growth differentiation factor gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0006290 proboscis IAGP N RGD:5509061 20160929 MGI PMID:22383895 1314355 Nodal nodal growth differentiation factor gene MP:0006323 abnormal extraembryonic mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:7924997 1314355 Nodal nodal growth differentiation factor gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23221368 1314355 Nodal nodal growth differentiation factor gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:1879365 1314355 Nodal nodal growth differentiation factor gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0008533 abnormal anterior visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0008786 abnormal hindgut morphology IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20160929 MGI PMID:22383895 1314355 Nodal nodal growth differentiation factor gene MP:0008926 abnormal anterior definitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:20508035 1314355 Nodal nodal growth differentiation factor gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:16950123 1314355 Nodal nodal growth differentiation factor gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:20508035 1314355 Nodal nodal growth differentiation factor gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20170314 MGI PMID:27466203 1314355 Nodal nodal growth differentiation factor gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:11456449 1314355 Nodal nodal growth differentiation factor gene MP:0009905 absent tongue IAGP N RGD:5509061 20171026 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1314355 Nodal nodal growth differentiation factor gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9655392 1314355 Nodal nodal growth differentiation factor gene MP:0010126 abnormal distal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15302604 1314355 Nodal nodal growth differentiation factor gene MP:0010335 fused first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0010335 fused first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:20508035 1314355 Nodal nodal growth differentiation factor gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:12231623 1314355 Nodal nodal growth differentiation factor gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:12231623 1314355 Nodal nodal growth differentiation factor gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:15454269 1314355 Nodal nodal growth differentiation factor gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:7924997 1314355 Nodal nodal growth differentiation factor gene MP:0010807 abnormal stomach position or orientation IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0010807 abnormal stomach position or orientation IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12231623 1314355 Nodal nodal growth differentiation factor gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12842913 1314355 Nodal nodal growth differentiation factor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1879365 1314355 Nodal nodal growth differentiation factor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8610012 1314355 Nodal nodal growth differentiation factor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10452853 1314355 Nodal nodal growth differentiation factor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12471260 1314355 Nodal nodal growth differentiation factor gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10518210 1314355 Nodal nodal growth differentiation factor gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16950123 1314355 Nodal nodal growth differentiation factor gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12842913 1314355 Nodal nodal growth differentiation factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314355 Nodal nodal growth differentiation factor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12842913 1314355 Nodal nodal growth differentiation factor gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12654299 1314355 Nodal nodal growth differentiation factor gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16564040 1314355 Nodal nodal growth differentiation factor gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0011203 abnormal parietal yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:1879365 1314355 Nodal nodal growth differentiation factor gene MP:0011206 absent visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:1879365 1314355 Nodal nodal growth differentiation factor gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:11456449 1314355 Nodal nodal growth differentiation factor gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0012081 absent heart tube IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:15454269 1314355 Nodal nodal growth differentiation factor gene MP:0012083 absent foregut IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0012084 truncated foregut IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:12842913 1314355 Nodal nodal growth differentiation factor gene MP:0012098 increased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:11456449 1314355 Nodal nodal growth differentiation factor gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:12842913 1314355 Nodal nodal growth differentiation factor gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:10452853 1314355 Nodal nodal growth differentiation factor gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20160929 MGI PMID:22383895 1314355 Nodal nodal growth differentiation factor gene MP:0012156 rostral-caudal axis duplication IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:12842913 1314355 Nodal nodal growth differentiation factor gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:15302604 1314355 Nodal nodal growth differentiation factor gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:9655392 1314355 Nodal nodal growth differentiation factor gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20160929 MGI PMID:22383895 1314355 Nodal nodal growth differentiation factor gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20170314 MGI PMID:27466203 1314355 Nodal nodal growth differentiation factor gene MP:0012160 expanded anterior visceral endoderm IAGP N RGD:5509061 20141003 MGI PMID:20573697 1314355 Nodal nodal growth differentiation factor gene MP:0012176 abnormal head development IAGP N RGD:5509061 20171109 MGI PMID:11311163 1314355 Nodal nodal growth differentiation factor gene MP:0012181 increased somite number IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 1314355 Nodal nodal growth differentiation factor gene MP:0012515 abnormal heart apex morphology IAGP N RGD:5509061 20141003 MGI PMID:12091315 1314355 Nodal nodal growth differentiation factor gene MP:0012675 enlarged floor plate IAGP N RGD:5509061 20141003 MGI PMID:18171685 1314355 Nodal nodal growth differentiation factor gene MP:0012706 decreased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12842913 1314355 Nodal nodal growth differentiation factor gene MP:0012724 absent head fold IAGP N RGD:5509061 20141003 MGI PMID:1879365 1314355 Nodal nodal growth differentiation factor gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1314355 Nodal nodal growth differentiation factor gene MP:0030198 nasal septum hypoplasia IAGP N RGD:5509061 20171012 MGI PMID:16564040 1314359 Olig3 oligodendrocyte transcription factor 3 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:19357274 1314359 Olig3 oligodendrocyte transcription factor 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:18829970 1314359 Olig3 oligodendrocyte transcription factor 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:18829970 1314359 Olig3 oligodendrocyte transcription factor 3 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18829970 1314359 Olig3 oligodendrocyte transcription factor 3 gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:15769945 1314359 Olig3 oligodendrocyte transcription factor 3 gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:19088088 1314359 Olig3 oligodendrocyte transcription factor 3 gene MP:0003684 abnormal inferior olivary complex morphology IAGP N RGD:5509061 20141003 MGI PMID:18829970 1314359 Olig3 oligodendrocyte transcription factor 3 gene MP:0004165 abnormal lateral geniculate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19357274 1314359 Olig3 oligodendrocyte transcription factor 3 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:18829970 1314359 Olig3 oligodendrocyte transcription factor 3 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:15769945 1314359 Olig3 oligodendrocyte transcription factor 3 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15769945 1314359 Olig3 oligodendrocyte transcription factor 3 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18829970 1314359 Olig3 oligodendrocyte transcription factor 3 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19088088 1314359 Olig3 oligodendrocyte transcription factor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18829970 1314359 Olig3 oligodendrocyte transcription factor 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19357274 1314361 Klk8 kallikrein related-peptidase 8 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1314361 Klk8 kallikrein related-peptidase 8 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1314361 Klk8 kallikrein related-peptidase 8 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:11273653 1314361 Klk8 kallikrein related-peptidase 8 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1314361 Klk8 kallikrein related-peptidase 8 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:11549709 1314361 Klk8 kallikrein related-peptidase 8 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:11549709 1314361 Klk8 kallikrein related-peptidase 8 gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11273653 1314361 Klk8 kallikrein related-peptidase 8 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11273653 1314361 Klk8 kallikrein related-peptidase 8 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:11273653 1314361 Klk8 kallikrein related-peptidase 8 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1314361 Klk8 kallikrein related-peptidase 8 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:11273653 1314361 Klk8 kallikrein related-peptidase 8 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:11273653 1314361 Klk8 kallikrein related-peptidase 8 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11549709 1314361 Klk8 kallikrein related-peptidase 8 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11273653 1314363 Csrnp1 cysteine-serine-rich nuclear protein 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314363 Csrnp1 cysteine-serine-rich nuclear protein 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314363 Csrnp1 cysteine-serine-rich nuclear protein 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17726538 1314363 Csrnp1 cysteine-serine-rich nuclear protein 1 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314363 Csrnp1 cysteine-serine-rich nuclear protein 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314363 Csrnp1 cysteine-serine-rich nuclear protein 1 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314363 Csrnp1 cysteine-serine-rich nuclear protein 1 gene MP:0009895 decreased palatine bone horizontal plate size IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314363 Csrnp1 cysteine-serine-rich nuclear protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17726538 1314363 Csrnp1 cysteine-serine-rich nuclear protein 1 gene MP:0030383 small presphenoid bone IAGP N RGD:5509061 20171207 MGI PMID:17143286 1314367 Tnn tenascin N gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0000119 abnormal tooth eruption IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 1314367 Tnn tenascin N gene MP:0000601 small liver IEA N RGD:5509061 20230601 MGI 1314367 Tnn tenascin N gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1314367 Tnn tenascin N gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1314367 Tnn tenascin N gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0001263 weight loss IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0002083 premature death IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0003668 abnormal periodontal ligament morphology IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0011940 decreased food intake IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0013250 abnormal dental pulp morphology IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0030131 abnormal periodontium morphology IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0030137 abnormal upper incisor morphology IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0030456 abnormal odontoblast differentiation IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0030471 abnormal ameloblast differentiation IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0030508 abnormal dental epithelium morphology IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0030542 abnormal dentin development IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314367 Tnn tenascin N gene MP:0030544 abnormal enamel development IAGP N RGD:5509061 20210506 MGI PMID:33552067 1314370 Alg3 ALG3 alpha-1,3- mannosyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1314371 Slc38a11 solute carrier family 38, member 11 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1314371 Slc38a11 solute carrier family 38, member 11 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1314371 Slc38a11 solute carrier family 38, member 11 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20231207 MGI 1314373 Brms1l breast cancer metastasis-suppressor 1-like gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20240523 MGI 1314373 Brms1l breast cancer metastasis-suppressor 1-like gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20240523 MGI 1314373 Brms1l breast cancer metastasis-suppressor 1-like gene MP:0005655 increased aggression IEA N RGD:5509061 20201022 MGI 1314373 Brms1l breast cancer metastasis-suppressor 1-like gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1314373 Brms1l breast cancer metastasis-suppressor 1-like gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20240523 MGI 1314377 Armc12 armadillo repeat containing 12 gene MP:0001925 male infertility IAGP N RGD:5509061 20210415 MGI PMID:33536340 1314377 Armc12 armadillo repeat containing 12 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20210415 MGI PMID:33536340 1314377 Armc12 armadillo repeat containing 12 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20210415 MGI PMID:33536340 1314377 Armc12 armadillo repeat containing 12 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20210415 MGI PMID:33536340 1314377 Armc12 armadillo repeat containing 12 gene MP:0014468 disorganized sperm mitochondrial sheath IAGP N RGD:5509061 20240613 MGI PMID:33536340 1314377 Armc12 armadillo repeat containing 12 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210415 MGI PMID:33536340 1314377 Armc12 armadillo repeat containing 12 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20210415 MGI PMID:33536340 1314377 Armc12 armadillo repeat containing 12 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20210415 MGI PMID:33536340 1314382 Rnf126 ring finger protein 126 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20240822 MGI PMID:36563124 1314382 Rnf126 ring finger protein 126 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20240822 MGI PMID:36563124 1314382 Rnf126 ring finger protein 126 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1314382 Rnf126 ring finger protein 126 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240822 MGI PMID:36563124 1314382 Rnf126 ring finger protein 126 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1314382 Rnf126 ring finger protein 126 gene MP:0012734 abnormal response to radiation IAGP N RGD:5509061 20240822 MGI PMID:36563124 1314384 Tsga13 testis specific gene A13 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20220811 MGI 1314384 Tsga13 testis specific gene A13 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1314384 Tsga13 testis specific gene A13 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20190502 MGI 1314386 Scarf2 scavenger receptor class F, member 2 gene MP:0004357 long tibia IEA N RGD:5509061 20160114 MGI 1314391 Myo1g myosin IG gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1314391 Myo1g myosin IG gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1314391 Myo1g myosin IG gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:25083865 1314391 Myo1g myosin IG gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24310084 1314391 Myo1g myosin IG gene MP:0003917 increased kidney weight IEA N RGD:5509061 20230601 MGI 1314391 Myo1g myosin IG gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20240523 MGI 1314391 Myo1g myosin IG gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:24310084 1314391 Myo1g myosin IG gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:24310084 1314391 Myo1g myosin IG gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 1314391 Myo1g myosin IG gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1314391 Myo1g myosin IG gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:24310084 1314391 Myo1g myosin IG gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1314391 Myo1g myosin IG gene MP:0014472 impaired B cell migration IAGP N RGD:5509061 20240613 MGI PMID:24310084 1314396 Alppl2 alkaline phosphatase, placental-like 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10767088 1314396 Alppl2 alkaline phosphatase, placental-like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9056646 1314396 Alppl2 alkaline phosphatase, placental-like 2 gene MP:0002293 long gestation period IAGP N RGD:5509061 20141003 MGI PMID:10767088 1314396 Alppl2 alkaline phosphatase, placental-like 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10767088 1314396 Alppl2 alkaline phosphatase, placental-like 2 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:10767088 1314396 Alppl2 alkaline phosphatase, placental-like 2 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10767088 1314402 Dnajc8 DnaJ heat shock protein family (Hsp40) member C8 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1314402 Dnajc8 DnaJ heat shock protein family (Hsp40) member C8 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1314402 Dnajc8 DnaJ heat shock protein family (Hsp40) member C8 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1314402 Dnajc8 DnaJ heat shock protein family (Hsp40) member C8 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1314402 Dnajc8 DnaJ heat shock protein family (Hsp40) member C8 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1314402 Dnajc8 DnaJ heat shock protein family (Hsp40) member C8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314402 Dnajc8 DnaJ heat shock protein family (Hsp40) member C8 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1314404 Naga N-acetyl galactosaminidase, alpha gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20201022 MGI 1314408 Epc1 enhancer of polycomb homolog 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20160804 MGI 1314408 Epc1 enhancer of polycomb homolog 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:19359245 1314408 Epc1 enhancer of polycomb homolog 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1314408 Epc1 enhancer of polycomb homolog 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1314408 Epc1 enhancer of polycomb homolog 1 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1314408 Epc1 enhancer of polycomb homolog 1 gene MP:0002944 increased lactate dehydrogenase level IEA N RGD:5509061 20160804 MGI 1314408 Epc1 enhancer of polycomb homolog 1 gene MP:0003062 abnormal coping response IEA N RGD:5509061 20160804 MGI 1314408 Epc1 enhancer of polycomb homolog 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1314408 Epc1 enhancer of polycomb homolog 1 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20160804 MGI 1314408 Epc1 enhancer of polycomb homolog 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19359245 1314409 Aifm3 apoptosis-inducing factor, mitochondrion-associated 3 gene MP:0000181 abnormal circulating LDL cholesterol level IEA N RGD:5509061 20211021 MGI 1314409 Aifm3 apoptosis-inducing factor, mitochondrion-associated 3 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20211021 MGI 1314409 Aifm3 apoptosis-inducing factor, mitochondrion-associated 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1314409 Aifm3 apoptosis-inducing factor, mitochondrion-associated 3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20181227 MGI 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20181227 MGI 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0001523 impaired righting response IEA N RGD:5509061 20181227 MGI 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0001956 hypopnea IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0003005 abnormal hippocampal fimbria morphology IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314411 Klf7 Kruppel-like transcription factor 7 (ubiquitous) gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15964824 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23963447 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23963447 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23963447 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:23963447 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18281502 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23963447 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:23963447 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:18281502 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0008121 increased myeloid dendritic cell number IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23963447 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23963447 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:23963447 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0010963 abnormal compact bone volume IAGP N RGD:5509061 20141003 MGI PMID:23963447 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0013693 abnormal hemopoiesis IAGP N RGD:5509061 20161124 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0030007 abnormal bone marrow adipose tissue morphology IAGP N RGD:5509061 20170706 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0030009 increased bone marrow adipose tissue amount IAGP N RGD:5509061 20170706 MGI PMID:27445989 1314414 Mfap2 microfibrillar-associated protein 2 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201001 MGI PMID:18281502 1314420 Epb41l4a erythrocyte membrane protein band 4.1 like 4a gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1314420 Epb41l4a erythrocyte membrane protein band 4.1 like 4a gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1314420 Epb41l4a erythrocyte membrane protein band 4.1 like 4a gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210826 MGI 1314420 Epb41l4a erythrocyte membrane protein band 4.1 like 4a gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1314420 Epb41l4a erythrocyte membrane protein band 4.1 like 4a gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210520 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0000826 abnormal third ventricle morphology IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0000914 exencephaly IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200806 MGI PMID:31677819 1314426 Coro1c coronin, actin binding protein 1C gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20200806 MGI PMID:31677819 1314426 Coro1c coronin, actin binding protein 1C gene MP:0002083 premature death IAGP N RGD:5509061 20200806 MGI PMID:31677819 1314426 Coro1c coronin, actin binding protein 1C gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20200806 MGI PMID:31677819 1314426 Coro1c coronin, actin binding protein 1C gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0003253 dilated bile duct IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0003595 epididymal cyst IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0004463 basisphenoid bone foramen IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20200806 MGI PMID:31677819 1314426 Coro1c coronin, actin binding protein 1C gene MP:0005274 abnormal viscerocranium morphology IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20200806 MGI PMID:31677819 1314426 Coro1c coronin, actin binding protein 1C gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0008922 abnormal cervical rib IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0009493 abnormal cystic duct morphology IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0009532 decreased parotid gland size IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0010490 abnormal inferior vena cava valve morphology IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0010727 increased glioblastoma incidence IAGP N RGD:5509061 20200806 MGI PMID:31677819 1314426 Coro1c coronin, actin binding protein 1C gene MP:0011536 decreased urination frequency IAGP N RGD:5509061 20200806 MGI PMID:31677819 1314426 Coro1c coronin, actin binding protein 1C gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200806 MGI PMID:31677819 1314426 Coro1c coronin, actin binding protein 1C gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0013968 multiple persisting craniopharyngeal ducts IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0013975 abnormal coronary sinus connection IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0014018 embryo tumor IEA N RGD:5509061 20170504 MGI 1314426 Coro1c coronin, actin binding protein 1C gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1314428 C1ql1 complement component 1, q subcomponent-like 1 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20170518 MGI PMID:25611509 1314428 C1ql1 complement component 1, q subcomponent-like 1 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20170518 MGI PMID:25611509 1314428 C1ql1 complement component 1, q subcomponent-like 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20170518 MGI PMID:25611509 1314428 C1ql1 complement component 1, q subcomponent-like 1 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20170518 MGI PMID:25611509 1314428 C1ql1 complement component 1, q subcomponent-like 1 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20170518 MGI PMID:25611509 1314431 Ttc38 tetratricopeptide repeat domain 38 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20240523 MGI 1314435 Dmrt3 doublesex and mab-3 related transcription factor 3 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:17803355 1314435 Dmrt3 doublesex and mab-3 related transcription factor 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20151217 MGI PMID:22932389 1314435 Dmrt3 doublesex and mab-3 related transcription factor 3 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20151217 MGI PMID:22932389 1314435 Dmrt3 doublesex and mab-3 related transcription factor 3 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20151217 MGI PMID:22932389 1314435 Dmrt3 doublesex and mab-3 related transcription factor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17803355 1314435 Dmrt3 doublesex and mab-3 related transcription factor 3 gene MP:0003880 abnormal central pattern generator function IAGP N RGD:5509061 20151217 MGI PMID:22932389 1314435 Dmrt3 doublesex and mab-3 related transcription factor 3 gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20141003 MGI PMID:17803355 1314435 Dmrt3 doublesex and mab-3 related transcription factor 3 gene MP:0004100 abnormal spinal cord interneuron morphology IAGP N RGD:5509061 20151217 MGI PMID:22932389 1314435 Dmrt3 doublesex and mab-3 related transcription factor 3 gene MP:0005424 jerky movement IAGP N RGD:5509061 20151217 MGI PMID:22932389 1314435 Dmrt3 doublesex and mab-3 related transcription factor 3 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23056351 1314435 Dmrt3 doublesex and mab-3 related transcription factor 3 gene MP:0010540 long stride length IAGP N RGD:5509061 20151217 MGI PMID:22932389 1314441 Reep5 receptor accessory protein 5 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1314444 Smox spermine oxidase gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170323 MGI 1314446 Gdap2 ganglioside-induced differentiation-associated-protein 2 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20200402 MGI 1314446 Gdap2 ganglioside-induced differentiation-associated-protein 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1314446 Gdap2 ganglioside-induced differentiation-associated-protein 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20181227 MGI 1314446 Gdap2 ganglioside-induced differentiation-associated-protein 2 gene MP:0005478 decreased circulating thyroxine level IEA N RGD:5509061 20181227 MGI 1314446 Gdap2 ganglioside-induced differentiation-associated-protein 2 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20211021 MGI 1314446 Gdap2 ganglioside-induced differentiation-associated-protein 2 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20201231 MGI 1314446 Gdap2 ganglioside-induced differentiation-associated-protein 2 gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20210128 MGI 1314446 Gdap2 ganglioside-induced differentiation-associated-protein 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200402 MGI 1314446 Gdap2 ganglioside-induced differentiation-associated-protein 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20181227 MGI 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0000231 hypertension IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0002708 nephrolithiasis IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0009810 increased urine uric acid level IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0010092 increased circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0011435 increased urine magnesium level IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0011537 uraturia IAGP N RGD:5509061 20141003 MGI PMID:19706426 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314451 Slc2a9 solute carrier family 2 (facilitated glucose transporter), member 9 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20160428 MGI PMID:25100214 1314453 Pea15a proliferation and apoptosis adaptor protein 15A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10493725 1314453 Pea15a proliferation and apoptosis adaptor protein 15A gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10493725 1314453 Pea15a proliferation and apoptosis adaptor protein 15A gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:17504918 1314454 Helz2 helicase with zinc finger 2, transcriptional coactivator gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20160218 MGI PMID:25004093 1314454 Helz2 helicase with zinc finger 2, transcriptional coactivator gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20160218 MGI PMID:25004093 1314454 Helz2 helicase with zinc finger 2, transcriptional coactivator gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160218 MGI PMID:25004093 1314454 Helz2 helicase with zinc finger 2, transcriptional coactivator gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20160218 MGI PMID:25004093 1314454 Helz2 helicase with zinc finger 2, transcriptional coactivator gene MP:0003948 abnormal gas homeostasis IAGP N RGD:5509061 20160218 MGI PMID:25004093 1314454 Helz2 helicase with zinc finger 2, transcriptional coactivator gene MP:0004848 abnormal liver size IAGP N RGD:5509061 20160218 MGI PMID:25004093 1314454 Helz2 helicase with zinc finger 2, transcriptional coactivator gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20160218 MGI PMID:25004093 1314454 Helz2 helicase with zinc finger 2, transcriptional coactivator gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20160218 MGI PMID:25004093 1314454 Helz2 helicase with zinc finger 2, transcriptional coactivator gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20160218 MGI PMID:25004093 1314454 Helz2 helicase with zinc finger 2, transcriptional coactivator gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20160218 MGI PMID:25004093 1314454 Helz2 helicase with zinc finger 2, transcriptional coactivator gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20160218 MGI PMID:25004093 1314454 Helz2 helicase with zinc finger 2, transcriptional coactivator gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20160218 MGI PMID:25004093 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200123 MGI PMID:27783952 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:16815997 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:16815997 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16815997 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:18854161 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20200123 MGI PMID:27783952 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20200123 MGI PMID:27783952 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20200123 MGI PMID:27783952 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0008221 abnormal hippocampal commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200123 MGI PMID:27783952 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:27783952 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0008583 absent photoreceptor inner segment IAGP N RGD:5509061 20200123 MGI PMID:27783952 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20200123 MGI PMID:27783952 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20200123 MGI PMID:27783952 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0010011 ectopic hippocampus pyramidal cells IAGP N RGD:5509061 20141003 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16815997 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20200123 MGI PMID:27783952 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200123 MGI PMID:27783952 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200123 MGI PMID:27783952 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200123 MGI PMID:27783952 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0012194 decreased keratinocyte migration IAGP N RGD:5509061 20141204 MGI PMID:18854161 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0013908 small lateral ventricles IAGP N RGD:5509061 20161103 MGI PMID:20170731 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20200123 MGI PMID:27783952 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0020439 absent b-wave IAGP N RGD:5509061 20200123 MGI PMID:27783952 1314455 Macf1 microtubule-actin crosslinking factor 1 gene MP:0030577 increased keratinocyte adhesion IAGP N RGD:5509061 20180607 MGI PMID:18854161 1314458 Onecut3 one cut domain, family member 3 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:17400205 1314458 Onecut3 one cut domain, family member 3 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:17400205 1314458 Onecut3 one cut domain, family member 3 gene MP:0009111 pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17400205 1314460 Pgm2 phosphoglucomutase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:162283 1314460 Pgm2 phosphoglucomutase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:6457600 1314462 Skic3 SKI3 subunit of superkiller complex gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1314462 Skic3 SKI3 subunit of superkiller complex gene MP:0001304 cataract IEA N RGD:5509061 20230601 MGI 1314462 Skic3 SKI3 subunit of superkiller complex gene MP:0001698 decreased embryo size IEA N RGD:5509061 20241010 MGI 1314462 Skic3 SKI3 subunit of superkiller complex gene MP:0002582 disorganized extraembryonic tissue IEA N RGD:5509061 20241010 MGI 1314462 Skic3 SKI3 subunit of superkiller complex gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20241010 MGI 1314462 Skic3 SKI3 subunit of superkiller complex gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241010 MGI 1314462 Skic3 SKI3 subunit of superkiller complex gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20230601 MGI 1314462 Skic3 SKI3 subunit of superkiller complex gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230601 MGI 1314462 Skic3 SKI3 subunit of superkiller complex gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1314462 Skic3 SKI3 subunit of superkiller complex gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1314462 Skic3 SKI3 subunit of superkiller complex gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20230601 MGI 1314462 Skic3 SKI3 subunit of superkiller complex gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230601 MGI 1314462 Skic3 SKI3 subunit of superkiller complex gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 1314463 Cep15 centrosomal protein 15 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230720 MGI 1314464 Dennd6a DENN domain containing 6A gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16157885 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16157885 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16157885 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16157885 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16157885 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16157885 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16157885 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16157885 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16157885 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16157885 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20220915 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:17227869 1314471 Arhgap1 Rho GTPase activating protein 1 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:17227869 1314473 Vrk1 vaccinia related kinase 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220224 MGI PMID:21277975 1314473 Vrk1 vaccinia related kinase 1 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20220407 MGI PMID:22741057 1314473 Vrk1 vaccinia related kinase 1 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220407 MGI PMID:22741057 1314473 Vrk1 vaccinia related kinase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19696012 1314473 Vrk1 vaccinia related kinase 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:19696012 1314473 Vrk1 vaccinia related kinase 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220224 MGI PMID:21277975 1314473 Vrk1 vaccinia related kinase 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19696012 1314473 Vrk1 vaccinia related kinase 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220224 MGI PMID:21277975 1314473 Vrk1 vaccinia related kinase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19696012 1314473 Vrk1 vaccinia related kinase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220224 MGI PMID:21277975 1314473 Vrk1 vaccinia related kinase 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19696012 1314473 Vrk1 vaccinia related kinase 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20220224 MGI PMID:21277975 1314473 Vrk1 vaccinia related kinase 1 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20220224 MGI PMID:21277975 1314473 Vrk1 vaccinia related kinase 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20220224 MGI PMID:21277975 1314473 Vrk1 vaccinia related kinase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19696012 1314473 Vrk1 vaccinia related kinase 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19696012 1314473 Vrk1 vaccinia related kinase 1 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:19696012 1314473 Vrk1 vaccinia related kinase 1 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20141003 MGI PMID:19696012 1314473 Vrk1 vaccinia related kinase 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1314473 Vrk1 vaccinia related kinase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220224 MGI PMID:21277975 1314473 Vrk1 vaccinia related kinase 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:19696012 1314473 Vrk1 vaccinia related kinase 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220224 MGI PMID:21277975 1314473 Vrk1 vaccinia related kinase 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 1314473 Vrk1 vaccinia related kinase 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:19696012 1314473 Vrk1 vaccinia related kinase 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20220224 MGI PMID:21277975 1314473 Vrk1 vaccinia related kinase 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220519 MGI 1314473 Vrk1 vaccinia related kinase 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:19696012 1314473 Vrk1 vaccinia related kinase 1 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20220224 MGI PMID:21277975 1314473 Vrk1 vaccinia related kinase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314473 Vrk1 vaccinia related kinase 1 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:22741057 1314473 Vrk1 vaccinia related kinase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1314473 Vrk1 vaccinia related kinase 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220519 MGI 1314473 Vrk1 vaccinia related kinase 1 gene MP:0014011 abnormal ovary tissue architecture IAGP N RGD:5509061 20220407 MGI PMID:22741057 1314473 Vrk1 vaccinia related kinase 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:21277975 1314473 Vrk1 vaccinia related kinase 1 gene MP:0014443 impaired polar body extrusion IAGP N RGD:5509061 20240509 MGI PMID:21277975 1314473 Vrk1 vaccinia related kinase 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1314473 Vrk1 vaccinia related kinase 1 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:22741057 1314475 Rom1 rod outer segment membrane protein 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:10802659 1314475 Rom1 rod outer segment membrane protein 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:20300562 1314475 Rom1 rod outer segment membrane protein 1 gene MP:0001326 retina degeneration IEA N RGD:5509061 20111116 MGI 1314475 Rom1 rod outer segment membrane protein 1 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:20300562 1314475 Rom1 rod outer segment membrane protein 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10802659 1314475 Rom1 rod outer segment membrane protein 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20300562 1314475 Rom1 rod outer segment membrane protein 1 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10802659 1314475 Rom1 rod outer segment membrane protein 1 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:10802659 1314475 Rom1 rod outer segment membrane protein 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:10802659 1314475 Rom1 rod outer segment membrane protein 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20300562 1314475 Rom1 rod outer segment membrane protein 1 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:20300562 1314475 Rom1 rod outer segment membrane protein 1 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:20300562 1314475 Rom1 rod outer segment membrane protein 1 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20300562 1314477 Inpp1 inositol polyphosphate-1-phosphatase gene MP:0001258 decreased body length IEA N RGD:5509061 20160804 MGI 1314477 Inpp1 inositol polyphosphate-1-phosphatase gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1314477 Inpp1 inositol polyphosphate-1-phosphatase gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1314477 Inpp1 inositol polyphosphate-1-phosphatase gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201231 MGI 1314477 Inpp1 inositol polyphosphate-1-phosphatase gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20160922 MGI PMID:24652767 1314477 Inpp1 inositol polyphosphate-1-phosphatase gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0001147 small testis IAGP N RGD:5509061 20201015 MGI PMID:32345962 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0001147 small testis IAGP N RGD:5509061 20201022 MGI PMID:32463460 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0001147 small testis IAGP N RGD:5509061 20220616 MGI PMID:32845237 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220616 MGI PMID:32845237 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20201015 MGI PMID:32345962 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20201022 MGI PMID:32463460 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220616 MGI PMID:32845237 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20201022 MGI PMID:32463460 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20201015 MGI PMID:32345962 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20201022 MGI PMID:32463460 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220616 MGI PMID:32845237 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20201015 MGI PMID:32345962 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20201022 MGI PMID:32463460 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20220616 MGI PMID:32845237 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20201022 MGI PMID:32463460 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20201022 MGI PMID:32463460 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20220616 MGI PMID:32845237 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20201015 MGI PMID:32345962 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20201015 MGI PMID:32345962 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20220616 MGI PMID:32845237 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20201015 MGI PMID:32345962 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20201022 MGI PMID:32463460 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20201015 MGI PMID:32345962 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20201015 MGI PMID:32345962 1314478 Brme1 break repair meiotic recombinase recruitment factor 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20201022 MGI PMID:32463460 1314479 Obsl1 obscurin-like 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20201217 MGI PMID:31098411 1314479 Obsl1 obscurin-like 1 gene MP:0002713 abnormal glycogen catabolism IAGP N RGD:5509061 20201217 MGI PMID:31098411 1314479 Obsl1 obscurin-like 1 gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20201217 MGI PMID:31098411 1314479 Obsl1 obscurin-like 1 gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20201217 MGI PMID:31098411 1314479 Obsl1 obscurin-like 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20201217 MGI PMID:31098411 1314479 Obsl1 obscurin-like 1 gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20201217 MGI PMID:31098411 1314479 Obsl1 obscurin-like 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20201217 MGI PMID:31098411 1314479 Obsl1 obscurin-like 1 gene MP:0009423 increased extensor digitorum longus weight IAGP N RGD:5509061 20201217 MGI PMID:31098411 1314479 Obsl1 obscurin-like 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20201217 MGI PMID:31098411 1314479 Obsl1 obscurin-like 1 gene MP:0012655 increased catalase level IAGP N RGD:5509061 20201217 MGI PMID:31098411 1314479 Obsl1 obscurin-like 1 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:31098411 1314480 Mymk myomaker, myoblast fusion factor gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:23868259 1314480 Mymk myomaker, myoblast fusion factor gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:23868259 1314480 Mymk myomaker, myoblast fusion factor gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:23868259 1314480 Mymk myomaker, myoblast fusion factor gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23868259 1314480 Mymk myomaker, myoblast fusion factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23868259 1314480 Mymk myomaker, myoblast fusion factor gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:23868259 1314480 Mymk myomaker, myoblast fusion factor gene MP:0030959 abnormal myoblast fusion IAGP N RGD:5509061 20190725 MGI PMID:23868259 1314482 Srp72 signal recognition particle 72 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230119 MGI 1314482 Srp72 signal recognition particle 72 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230119 MGI 1314482 Srp72 signal recognition particle 72 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230119 MGI 1314482 Srp72 signal recognition particle 72 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1314482 Srp72 signal recognition particle 72 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230119 MGI 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:16446448 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16446448 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:16446448 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:16446448 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:16446448 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:16446448 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16446448 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:16446448 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16446448 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16446448 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16446448 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0002933 joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:16446448 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16446448 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20160804 MGI PMID:22914735 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16446448 1314486 Neil1 nei endonuclease VIII-like 1 (E. coli) gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16446448 1314488 Cyp2s1 cytochrome P450, family 2, subfamily s, polypeptide 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23073733 1314491 Blvrb biliverdin reductase B gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20211021 MGI 1314491 Blvrb biliverdin reductase B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1314491 Blvrb biliverdin reductase B gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1314494 Cabp4 calcium binding protein 4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1314494 Cabp4 calcium binding protein 4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1314494 Cabp4 calcium binding protein 4 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15452577 1314494 Cabp4 calcium binding protein 4 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15452577 1314494 Cabp4 calcium binding protein 4 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:15452577 1314494 Cabp4 calcium binding protein 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1314494 Cabp4 calcium binding protein 4 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20181227 MGI 1314494 Cabp4 calcium binding protein 4 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20181227 MGI 1314494 Cabp4 calcium binding protein 4 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15452577 1314494 Cabp4 calcium binding protein 4 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15452577 1314494 Cabp4 calcium binding protein 4 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:15452577 1314494 Cabp4 calcium binding protein 4 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15452577 1314494 Cabp4 calcium binding protein 4 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15452577 1314494 Cabp4 calcium binding protein 4 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15452577 1314494 Cabp4 calcium binding protein 4 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15452577 1314494 Cabp4 calcium binding protein 4 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:15452577 1314494 Cabp4 calcium binding protein 4 gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:15452577 1314500 Riok1 RIO kinase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314500 Riok1 RIO kinase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1314500 Riok1 RIO kinase 1 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240801 MGI 1314502 Auh AU RNA binding protein/enoyl-coenzyme A hydratase gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20181227 MGI 1314502 Auh AU RNA binding protein/enoyl-coenzyme A hydratase gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1314502 Auh AU RNA binding protein/enoyl-coenzyme A hydratase gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20221215 MGI 1314504 Sfxn4 sideroflexin 4 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210520 MGI 1314510 Arhgap31 Rho GTPase activating protein 31 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20211028 MGI PMID:27270835 1314510 Arhgap31 Rho GTPase activating protein 31 gene MP:0000603 pale liver IAGP N RGD:5509061 20211028 MGI PMID:27270835 1314510 Arhgap31 Rho GTPase activating protein 31 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20211028 MGI PMID:27270835 1314510 Arhgap31 Rho GTPase activating protein 31 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1314510 Arhgap31 Rho GTPase activating protein 31 gene MP:0001785 edema IEA N RGD:5509061 20221215 MGI 1314510 Arhgap31 Rho GTPase activating protein 31 gene MP:0001914 hemorrhage IEA N RGD:5509061 20221215 MGI 1314510 Arhgap31 Rho GTPase activating protein 31 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20211028 MGI PMID:27270835 1314510 Arhgap31 Rho GTPase activating protein 31 gene MP:0009022 abnormal brain meninges morphology IAGP N RGD:5509061 20211028 MGI PMID:27270835 1314510 Arhgap31 Rho GTPase activating protein 31 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1314510 Arhgap31 Rho GTPase activating protein 31 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1314510 Arhgap31 Rho GTPase activating protein 31 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20211028 MGI PMID:27270835 1314510 Arhgap31 Rho GTPase activating protein 31 gene MP:0013848 subcutaneous edema IAGP N RGD:5509061 20211028 MGI PMID:27270835 1314510 Arhgap31 Rho GTPase activating protein 31 gene MP:0031152 subcutaneous hemorrhage IAGP N RGD:5509061 20211028 MGI PMID:27270835 1314516 Dop1b DOP1 leucine zipper like protein B gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20150108 MGI 1314516 Dop1b DOP1 leucine zipper like protein B gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1314516 Dop1b DOP1 leucine zipper like protein B gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201022 MGI 1314516 Dop1b DOP1 leucine zipper like protein B gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20211021 MGI 1314516 Dop1b DOP1 leucine zipper like protein B gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20150108 MGI 1314516 Dop1b DOP1 leucine zipper like protein B gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1314516 Dop1b DOP1 leucine zipper like protein B gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1314516 Dop1b DOP1 leucine zipper like protein B gene MP:0010052 increased grip strength IEA N RGD:5509061 20181227 MGI 1314516 Dop1b DOP1 leucine zipper like protein B gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1314517 Sae1 SUMO1 activating enzyme subunit 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1314521 Cmip c-Maf inducing protein gene MP:0000489 abnormal large intestine morphology IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0000496 abnormal small intestine morphology IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0001879 abnormal lymphatic vessel morphology IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0002951 small thyroid gland IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0003262 intestinal/bowel diverticulum IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0004160 retroesophageal right subclavian artery IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0009820 abnormal liver vasculature morphology IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314521 Cmip c-Maf inducing protein gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0013963 jugular vein stenosis IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0013968 multiple persisting craniopharyngeal ducts IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0013975 abnormal coronary sinus connection IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0014018 embryo tumor IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0014019 embryo cyst IEA N RGD:5509061 20170504 MGI 1314521 Cmip c-Maf inducing protein gene MP:0020500 persistent trigeminal artery IEA N RGD:5509061 20180628 MGI 1314536 Eif3f eukaryotic translation initiation factor 3, subunit F gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200514 MGI 1314536 Eif3f eukaryotic translation initiation factor 3, subunit F gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20201015 MGI PMID:31026345 1314536 Eif3f eukaryotic translation initiation factor 3, subunit F gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20201015 MGI PMID:31026345 1314536 Eif3f eukaryotic translation initiation factor 3, subunit F gene MP:0004065 increased susceptibility to induced muscular atrophy IAGP N RGD:5509061 20201015 MGI PMID:31026345 1314536 Eif3f eukaryotic translation initiation factor 3, subunit F gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20201015 MGI PMID:31026345 1314536 Eif3f eukaryotic translation initiation factor 3, subunit F gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20201015 MGI PMID:31026345 1314536 Eif3f eukaryotic translation initiation factor 3, subunit F gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20201015 MGI PMID:31026345 1314536 Eif3f eukaryotic translation initiation factor 3, subunit F gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20201015 MGI PMID:31026345 1314536 Eif3f eukaryotic translation initiation factor 3, subunit F gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314536 Eif3f eukaryotic translation initiation factor 3, subunit F gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20201015 MGI PMID:31026345 1314536 Eif3f eukaryotic translation initiation factor 3, subunit F gene MP:0013272 abnormal translation IAGP N RGD:5509061 20201015 MGI PMID:31026345 1314538 Fjx1 four jointed box 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:18604206 1314538 Fjx1 four jointed box 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1314538 Fjx1 four jointed box 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18028897 1314538 Fjx1 four jointed box 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:18604206 1314538 Fjx1 four jointed box 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18604206 1314538 Fjx1 four jointed box 1 gene MP:0004017 duplex kidney IAGP N RGD:5509061 20141003 MGI PMID:18604206 1314538 Fjx1 four jointed box 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21903076 1314538 Fjx1 four jointed box 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18028897 1314538 Fjx1 four jointed box 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1314538 Fjx1 four jointed box 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18604206 1314538 Fjx1 four jointed box 1 gene MP:0011493 double ureter IAGP N RGD:5509061 20141003 MGI PMID:18604206 1314543 Fhip2a FHF complex subunit HOOK interacting protein 2A gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230601 MGI 1314543 Fhip2a FHF complex subunit HOOK interacting protein 2A gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1314543 Fhip2a FHF complex subunit HOOK interacting protein 2A gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1314543 Fhip2a FHF complex subunit HOOK interacting protein 2A gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1314543 Fhip2a FHF complex subunit HOOK interacting protein 2A gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230601 MGI 1314543 Fhip2a FHF complex subunit HOOK interacting protein 2A gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20230601 MGI 1314546 Enox1 ecto-NOX disulfide-thiol exchanger 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1314546 Enox1 ecto-NOX disulfide-thiol exchanger 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20221215 MGI 1314546 Enox1 ecto-NOX disulfide-thiol exchanger 1 gene MP:0011954 shortened PQ interval IEA N RGD:5509061 20220519 MGI 1314548 Mideas mitotic deacetylase associated SANT domain protein gene MP:0000215 absent erythrocytes IAGP N RGD:5509061 20201224 MGI PMID:32591534 1314548 Mideas mitotic deacetylase associated SANT domain protein gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20201224 MGI PMID:32591534 1314548 Mideas mitotic deacetylase associated SANT domain protein gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20201224 MGI PMID:32591534 1314548 Mideas mitotic deacetylase associated SANT domain protein gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20201224 MGI PMID:32591534 1314548 Mideas mitotic deacetylase associated SANT domain protein gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20201224 MGI PMID:32591534 1314548 Mideas mitotic deacetylase associated SANT domain protein gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20201224 MGI PMID:32591534 1314548 Mideas mitotic deacetylase associated SANT domain protein gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20201224 MGI PMID:32591534 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000023 abnormal ear position IAGP N RGD:5509061 20170209 MGI PMID:8387379 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20170209 MGI PMID:19906844 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20170209 MGI PMID:20570969 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000075 absent neurocranium IAGP N RGD:5509061 20171102 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20170209 MGI PMID:7202526 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20170209 MGI PMID:15728667 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20170209 MGI PMID:23792766 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20170209 MGI PMID:19549984 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20170209 MGI PMID:5806166 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20170209 MGI PMID:19549984 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20170209 MGI PMID:23792766 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000288 abnormal pericardium morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000373 belly spot IAGP N RGD:5509061 20170209 MGI PMID:18397875 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000373 belly spot IAGP N RGD:5509061 20170209 MGI PMID:5806166 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000413 polyphalangy IAGP N RGD:5509061 20170209 MGI PMID:17400206 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000413 polyphalangy IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20170209 MGI PMID:12112872 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20170209 MGI PMID:23645682 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000547 short limbs IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000547 short limbs IAGP N RGD:5509061 20170209 MGI PMID:19906844 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000547 short limbs IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000553 absent radius IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000553 absent radius IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000561 adactyly IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:10725236 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:11748151 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:12112872 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:12385751 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:12435627 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:17266131 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:17400206 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:17504940 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:19223390 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:19549984 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:1983115 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:20386744 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:22465667 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:23792766 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:24700818 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:6062373 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:7202526 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:7628698 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:8387379 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170209 MGI PMID:9268572 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000564 syndactyly IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000564 syndactyly IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000564 syndactyly IAGP N RGD:5509061 20170209 MGI PMID:5806166 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000564 syndactyly IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000564 syndactyly IAGP N RGD:5509061 20170209 MGI PMID:8387379 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000566 synostosis IAGP N RGD:5509061 20170209 MGI PMID:17400206 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000566 synostosis IAGP N RGD:5509061 20170209 MGI PMID:7202526 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20170209 MGI PMID:17400206 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20170209 MGI PMID:20386744 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20170209 MGI PMID:9268572 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20170209 MGI PMID:12112872 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20170209 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20170209 MGI PMID:7976186 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20170209 MGI PMID:9232833 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20170209 MGI PMID:2323034 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20190228 MGI PMID:2323034 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20190228 MGI PMID:8026071 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20170209 MGI PMID:7976186 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20170209 MGI PMID:7976186 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20190228 MGI PMID:8026071 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20190228 MGI PMID:8026071 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20170209 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20170209 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20170209 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20170209 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20170209 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20170209 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20170209 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20170209 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20170209 MGI PMID:12112872 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20170209 MGI PMID:19549984 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20170209 MGI PMID:22383895 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20170209 MGI PMID:5806166 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20170209 MGI PMID:7202526 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20170209 MGI PMID:8387379 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20170209 MGI PMID:22698544 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20170209 MGI PMID:14723851 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20170209 MGI PMID:7976186 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20170209 MGI PMID:8387379 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20170209 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20170209 MGI PMID:18397875 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20170209 MGI PMID:7976186 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000935 abnormal folding of telencephalic vesicles IAGP N RGD:5509061 20170209 MGI PMID:7976186 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20170209 MGI PMID:14723851 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20170209 MGI PMID:14723851 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20170209 MGI PMID:15215207 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20170209 MGI PMID:14723851 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001181 absent lungs IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20170209 MGI PMID:16720875 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170209 MGI PMID:19906844 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20170209 MGI PMID:8387379 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20170209 MGI PMID:12112872 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20170209 MGI PMID:12112872 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20170209 MGI PMID:7202526 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20170209 MGI PMID:12112872 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001678 thick apical ectodermal ridge IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001699 increased embryo size IAGP N RGD:5509061 20170209 MGI PMID:9268579 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001785 edema IAGP N RGD:5509061 20170209 MGI PMID:19549984 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001785 edema IAGP N RGD:5509061 20170209 MGI PMID:5806166 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001785 edema IAGP N RGD:5509061 20170209 MGI PMID:8387379 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001785 edema IAGP N RGD:5509061 20170209 MGI PMID:9268579 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001786 skin edema IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20170209 MGI PMID:12112872 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20170209 MGI PMID:2323034 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20190228 MGI PMID:8026071 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001925 male infertility IAGP N RGD:5509061 20170209 MGI PMID:11748151 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20170209 MGI PMID:12112872 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20170209 MGI 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20170209 MGI PMID:12112872 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20170209 MGI PMID:18397875 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20170209 MGI PMID:7202526 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002083 premature death IAGP N RGD:5509061 20170209 MGI PMID:11748151 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20170209 MGI PMID:16720875 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20170209 MGI PMID:22465667 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20170209 MGI PMID:8387379 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20170209 MGI PMID:12112872 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20170209 MGI PMID:17400206 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20170209 MGI PMID:17400206 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20170209 MGI PMID:5806166 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20170209 MGI PMID:6062373 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20170209 MGI PMID:7202526 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20170209 MGI PMID:12435627 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20170209 MGI PMID:19666503 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20180215 MGI PMID:28817564 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20170209 MGI PMID:12385751 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20170209 MGI PMID:22465667 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20170209 MGI PMID:8387379 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20170209 MGI PMID:12112872 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20170209 MGI PMID:2323034 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20190228 MGI PMID:8026071 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002256 abnormal laryngeal cartilage morphology IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20170209 MGI PMID:6062373 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20170209 MGI PMID:7976186 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20170209 MGI PMID:2323034 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20190228 MGI PMID:8026071 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002671 belted IAGP N RGD:5509061 20170209 MGI PMID:18397875 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002728 absent tibia IAGP N RGD:5509061 20170209 MGI PMID:17400206 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002728 absent tibia IAGP N RGD:5509061 20170209 MGI PMID:23792766 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002728 absent tibia IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002764 short tibia IAGP N RGD:5509061 20170209 MGI PMID:17400206 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002764 short tibia IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002764 short tibia IAGP N RGD:5509061 20170209 MGI PMID:23792766 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002764 short tibia IAGP N RGD:5509061 20170209 MGI PMID:7202526 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002764 short tibia IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002765 short fibula IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002765 short fibula IAGP N RGD:5509061 20170209 MGI PMID:7202526 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002765 short fibula IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003006 abnormal hippocampal fornix morphology IAGP N RGD:5509061 20190228 MGI PMID:8026071 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003052 omphalocele IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003109 short femur IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003109 short femur IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003109 short femur IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003130 anal atresia IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003160 abnormal esophagus development IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20170209 MGI PMID:22383895 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003276 esophageal atresia IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20170209 MGI PMID:23792766 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20170209 MGI PMID:2323034 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20170209 MGI PMID:7976186 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20170209 MGI PMID:9232833 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20190228 MGI PMID:8026071 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003604 single kidney IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003641 small lung IAGP N RGD:5509061 20170209 MGI PMID:9268579 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20170209 MGI PMID:9232833 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20170209 MGI PMID:5806166 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003841 abnormal lambdoid suture morphology IAGP N RGD:5509061 20170209 MGI PMID:20570969 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003854 abnormal forelimb stylopod morphology IAGP N RGD:5509061 20170209 MGI PMID:20386744 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20170209 MGI PMID:20386744 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20170209 MGI PMID:8387379 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20170209 MGI PMID:19223390 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20170209 MGI PMID:6062373 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004135 abnormal mammary gland embryonic development IAGP N RGD:5509061 20170209 MGI PMID:16914490 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20170209 MGI PMID:19906844 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004320 split sternum IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004321 short sternum IAGP N RGD:5509061 20170209 MGI PMID:5806166 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004340 short scapula IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004342 scapular bone foramen IAGP N RGD:5509061 20170209 MGI PMID:15728667 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004343 small scapula IAGP N RGD:5509061 20170209 MGI PMID:15728667 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004351 short humerus IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004351 short humerus IAGP N RGD:5509061 20170209 MGI PMID:23792766 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004351 short humerus IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004355 short radius IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004355 short radius IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004359 short ulna IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004359 short ulna IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004360 absent ulna IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004372 bowed fibula IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004374 bowed radius IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004374 bowed radius IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004457 abnormal orbitosphenoid bone morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004506 abnormal pubis morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004537 abnormal palatine bone horizontal plate morphology IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004544 absent esophagus IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004576 abnormal embryonic autopod plate morphology IAGP N RGD:5509061 20170209 MGI PMID:8387379 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004622 sacral vertebral fusion IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20170209 MGI PMID:23792766 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20170209 MGI PMID:14723851 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004979 abnormal neuronal precursor cell number IAGP N RGD:5509061 20170209 MGI PMID:14723851 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20170209 MGI PMID:14723851 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20170209 MGI PMID:2323034 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20190228 MGI PMID:8026071 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005237 abnormal olfactory tract morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20170209 MGI PMID:17400206 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20170209 MGI PMID:6062373 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20170209 MGI PMID:18397875 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005430 absent fibula IAGP N RGD:5509061 20170209 MGI PMID:23792766 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20170209 MGI PMID:12112872 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20170209 MGI PMID:9268579 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20170209 MGI PMID:9232833 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20170209 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20170209 MGI PMID:9232833 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20170209 MGI PMID:20386744 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20170209 MGI PMID:1983115 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0006292 abnormal nasal placode morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0006322 abnormal perichondrium morphology IAGP N RGD:5509061 20170209 MGI PMID:19906844 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0006343 enlarged first pharyngeal arch IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008160 increased diameter of humerus IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008161 increased diameter of radius IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008163 increased diameter of ulna IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20170209 MGI PMID:2323034 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20170209 MGI PMID:2323034 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20190228 MGI PMID:8026071 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20170209 MGI PMID:23792766 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008275 failure of endochondral bone ossification IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20190228 MGI PMID:8026071 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20170209 MGI PMID:2323034 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20170209 MGI PMID:7976186 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20170209 MGI PMID:18397875 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20170209 MGI PMID:22383895 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008818 abnormal interfrontal bone morphology IAGP N RGD:5509061 20170209 MGI PMID:5806166 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008818 abnormal interfrontal bone morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008854 bleb IAGP N RGD:5509061 20170209 MGI PMID:5806166 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008919 fused tarsal bones IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0008985 hemimelia IAGP N RGD:5509061 20170209 MGI PMID:23792766 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009003 abnormal vibrissa number IAGP N RGD:5509061 20170209 MGI PMID:8387379 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20170209 MGI PMID:11748151 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009039 absent inferior colliculus IAGP N RGD:5509061 20170209 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009048 enlarged tectum IAGP N RGD:5509061 20170209 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009049 abnormal hallux morphology IAGP N RGD:5509061 20170209 MGI PMID:5806166 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009049 abnormal hallux morphology IAGP N RGD:5509061 20170209 MGI PMID:6062373 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009569 abnormal left lung morphology IAGP N RGD:5509061 20170209 MGI PMID:9268579 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009571 abnormal right lung accessory lobe morphology IAGP N RGD:5509061 20170209 MGI PMID:9268579 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009573 abnormal right lung middle lobe morphology IAGP N RGD:5509061 20170209 MGI PMID:9268579 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009574 abnormal right lung caudal lobe morphology IAGP N RGD:5509061 20170209 MGI PMID:9268579 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20180301 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20170209 MGI PMID:12112872 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20170209 MGI PMID:20386744 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009744 postaxial polydactyly IAGP N RGD:5509061 20170209 MGI PMID:20386744 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009770 abnormal optic chiasm morphology IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20170209 MGI PMID:18397875 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20170209 MGI PMID:14723851 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20170209 MGI PMID:5806166 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0010883 trachea stenosis IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0010885 absent trachea IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0010906 abnormal lung bud morphology IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:17266131 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:17400206 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:19906844 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:8387379 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:9006072 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:6062373 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:16914490 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:19223390 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:8387379 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:9268579 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011238 abnormal inner ear development IAGP N RGD:5509061 20240822 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20170209 MGI PMID:22383895 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011362 ectopic adrenal gland IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011505 camptomelia IAGP N RGD:5509061 20170209 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011727 ectopic ovary IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0011964 increased total retina thickness IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0012101 acoria IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20170209 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0012139 increased forebrain size IAGP N RGD:5509061 20171207 MGI PMID:20570969 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0012260 encephalomeningocele IAGP N RGD:5509061 20190228 MGI PMID:8026071 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0012667 split sternal manubrium IAGP N RGD:5509061 20170209 MGI PMID:7202526 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0012706 decreased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20170209 MGI PMID:22383895 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0013261 absent epiglottis IAGP N RGD:5509061 20181108 MGI PMID:11978771 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0013362 absent pineal gland IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0013362 absent pineal gland IAGP N RGD:5509061 20190228 MGI PMID:8026071 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0013443 Harderian gland hyperplasia IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0013496 abnormal trachea development IAGP N RGD:5509061 20170209 MGI PMID:9731531 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0013529 decreased nipple number IAGP N RGD:5509061 20170209 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0013720 abnormal mammary line morphology IAGP N RGD:5509061 20170209 MGI PMID:16720875 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0013721 abnormal mammary placode morphology IAGP N RGD:5509061 20170209 MGI PMID:16914490 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0013785 abnormal mammary gland bud morphology IAGP N RGD:5509061 20170209 MGI PMID:16720875 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0013785 abnormal mammary gland bud morphology IAGP N RGD:5509061 20170209 MGI PMID:16914490 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0014291 decreased autopod size IAGP N RGD:5509061 20230824 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:23644062 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0021101 abnormal ventral interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:14723851 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0021101 abnormal ventral interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:15215207 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0021102 abnormal ventral interneuron 0 morphology IAGP N RGD:5509061 20220310 MGI PMID:15215207 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0021103 abnormal ventral interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:15215207 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:15215207 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:14723851 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:15215207 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0030031 abnormal forehead morphology IAGP N RGD:5509061 20171123 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0030203 short nasal septum IAGP N RGD:5509061 20171012 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0030205 thick nasal septum IAGP N RGD:5509061 20171012 MGI PMID:6049666 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0030353 wide sagittal suture IAGP N RGD:5509061 20171207 MGI PMID:20570969 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0030356 premature lambdoid suture closure IAGP N RGD:5509061 20171207 MGI PMID:20570969 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0030431 wide metopic suture IAGP N RGD:5509061 20171214 MGI PMID:20570969 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0030833 small acromion IAGP N RGD:5509061 20181018 MGI PMID:15728667 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0031442 enlarged cerebral aqueduct IAGP N RGD:5509061 20221103 MGI PMID:18480159 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0031447 unilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:5806166 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:5806166 1314554 Gli3 GLI-Kruppel family member GLI3 gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:6049666 1314559 Anapc5 anaphase-promoting complex subunit 5 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 1314559 Anapc5 anaphase-promoting complex subunit 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1314562 Pip5k1a phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:22321832 1314562 Pip5k1a phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:22321832 1314562 Pip5k1a phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:22321832 1314562 Pip5k1a phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22321832 1314562 Pip5k1a phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:22321832 1314562 Pip5k1a phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1314562 Pip5k1a phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22321832 1314562 Pip5k1a phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22321832 1314562 Pip5k1a phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20141003 MGI PMID:22321832 1314562 Pip5k1a phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22321832 1314562 Pip5k1a phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:22321832 1314562 Pip5k1a phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:22321832 1314562 Pip5k1a phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:22321832 1314562 Pip5k1a phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:22321832 1314562 Pip5k1a phosphatidylinositol-4-phosphate 5-kinase, type 1 alpha gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22321832 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20141003 MGI 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20141003 MGI 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20150430 MGI 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20141003 MGI 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20180503 MGI PMID:26526197 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20180503 MGI PMID:26526197 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0004092 absent Z line IAGP N RGD:5509061 20180503 MGI PMID:26526197 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0004093 diffuse Z line IAGP N RGD:5509061 20180503 MGI PMID:26526197 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0004146 absent M line IAGP N RGD:5509061 20180503 MGI PMID:26526197 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20180531 MGI PMID:26526197 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20211021 MGI 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0010759 decreased right ventricle systolic pressure IAGP N RGD:5509061 20180503 MGI PMID:26526197 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0030566 abnormal A band morphology IAGP N RGD:5509061 20180531 MGI PMID:26526197 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0030567 abnormal I band morphology IAGP N RGD:5509061 20180531 MGI PMID:26526197 1314564 Daam2 dishevelled associated activator of morphogenesis 2 gene MP:0030568 abnormal H zone morphology IAGP N RGD:5509061 20180531 MGI PMID:26526197 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0014391 increased hepatocyte mitochondrial DNA content IAGP N RGD:5509061 20240328 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314566 Thrap3 thyroid hormone receptor associated protein 3 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20231012 MGI PMID:37524868 1314568 Ovol2 ovo like zinc finger 2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0002188 small heart IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0004387 abnormal prechordal plate morphology IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0006305 abnormal optic eminence morphology IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0008786 abnormal hindgut morphology IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0010432 common ventricle IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0012155 abnormal optic pit morphology IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0012254 absent intersomitic vessels IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0012510 abnormal aortic sac morphology IAGP N RGD:5509061 20200310 MGI PMID:17573777 1314568 Ovol2 ovo like zinc finger 2 gene MP:0012532 abnormal surface ectoderm morphology IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0012702 increased embryonic neuroepithelium thickness IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0012706 decreased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0012744 increased neural crest cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0012746 abnormal neural crest cell delamination IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314568 Ovol2 ovo like zinc finger 2 gene MP:0030061 absent otic pit IAGP N RGD:5509061 20200310 MGI PMID:16423343 1314572 Ly6d lymphocyte antigen 6 family member D gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220811 MGI 1314574 Lsp1 lymphocyte specific 1 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:10961883 1314574 Lsp1 lymphocyte specific 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10961883 1314574 Lsp1 lymphocyte specific 1 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11261799 1314574 Lsp1 lymphocyte specific 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:10961883 1314574 Lsp1 lymphocyte specific 1 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:11261799 1314574 Lsp1 lymphocyte specific 1 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:15684321 1314576 Smarcal1 SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:22378147 1314576 Smarcal1 SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22378147 1314576 Smarcal1 SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22378147 1314576 Smarcal1 SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22378147 1314576 Smarcal1 SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:22378147 1314576 Smarcal1 SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1314576 Smarcal1 SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22378147 1314576 Smarcal1 SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:22378147 1314576 Smarcal1 SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:22378147 1314576 Smarcal1 SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22378147 1314576 Smarcal1 SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1314576 Smarcal1 SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160804 MGI 1314576 Smarcal1 SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22378147 1314576 Smarcal1 SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22378147 1314576 Smarcal1 SWI/SNF related matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22378147 1314580 Acsf3 acyl-CoA synthetase family member 3 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20230601 MGI 1314585 Tdrd1 tudor domain containing 1 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17038506 1314585 Tdrd1 tudor domain containing 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17038506 1314585 Tdrd1 tudor domain containing 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17038506 1314585 Tdrd1 tudor domain containing 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17038506 1314585 Tdrd1 tudor domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17038506 1314585 Tdrd1 tudor domain containing 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:17038506 1314585 Tdrd1 tudor domain containing 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17038506 1314585 Tdrd1 tudor domain containing 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17038506 1314585 Tdrd1 tudor domain containing 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:17038506 1314585 Tdrd1 tudor domain containing 1 gene MP:0031620 abnormal chromatoid body morphology IAGP N RGD:5509061 20240613 MGI PMID:17038506 1314587 Evpl envoplakin gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20141003 MGI PMID:11564887 1314590 Tbc1d24 TBC1 domain family, member 24 gene MP:0002064 seizures IAGP N RGD:5509061 20210121 MGI PMID:32987832 1314590 Tbc1d24 TBC1 domain family, member 24 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20190912 MGI PMID:30335140 1314590 Tbc1d24 TBC1 domain family, member 24 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20190912 MGI PMID:30335140 1314590 Tbc1d24 TBC1 domain family, member 24 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20190613 MGI PMID:30602030 1314590 Tbc1d24 TBC1 domain family, member 24 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20190912 MGI PMID:30335140 1314590 Tbc1d24 TBC1 domain family, member 24 gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20190912 MGI PMID:30335140 1314590 Tbc1d24 TBC1 domain family, member 24 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20190912 MGI PMID:30335140 1314590 Tbc1d24 TBC1 domain family, member 24 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20190912 MGI PMID:30335140 1314590 Tbc1d24 TBC1 domain family, member 24 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20190613 MGI PMID:30602030 1314590 Tbc1d24 TBC1 domain family, member 24 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210121 MGI PMID:32987832 1314590 Tbc1d24 TBC1 domain family, member 24 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20190613 MGI PMID:30602030 1314590 Tbc1d24 TBC1 domain family, member 24 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210121 MGI PMID:32987832 1314590 Tbc1d24 TBC1 domain family, member 24 gene MP:0030951 abnormal endocytosis IAGP N RGD:5509061 20190912 MGI PMID:30335140 1314595 Pask PAS domain containing serine/threonine kinase gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17878307 1314595 Pask PAS domain containing serine/threonine kinase gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:17878307 1314595 Pask PAS domain containing serine/threonine kinase gene MP:0002338 abnormal pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:18509100 1314595 Pask PAS domain containing serine/threonine kinase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17878307 1314595 Pask PAS domain containing serine/threonine kinase gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:17878307 1314595 Pask PAS domain containing serine/threonine kinase gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17878307 1314595 Pask PAS domain containing serine/threonine kinase gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18509100 1314595 Pask PAS domain containing serine/threonine kinase gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:17878307 1314595 Pask PAS domain containing serine/threonine kinase gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:17878307 1314595 Pask PAS domain containing serine/threonine kinase gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17878307 1314595 Pask PAS domain containing serine/threonine kinase gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17878307 1314595 Pask PAS domain containing serine/threonine kinase gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17878307 1314595 Pask PAS domain containing serine/threonine kinase gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:17878307 1314599 Ecpas Ecm29 proteasome adaptor and scaffold gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1314599 Ecpas Ecm29 proteasome adaptor and scaffold gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1314599 Ecpas Ecm29 proteasome adaptor and scaffold gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1314599 Ecpas Ecm29 proteasome adaptor and scaffold gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1314599 Ecpas Ecm29 proteasome adaptor and scaffold gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200213 MGI PMID:31910261 1314599 Ecpas Ecm29 proteasome adaptor and scaffold gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20200213 MGI PMID:31910261 1314599 Ecpas Ecm29 proteasome adaptor and scaffold gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20200213 MGI PMID:31910261 1314599 Ecpas Ecm29 proteasome adaptor and scaffold gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1314599 Ecpas Ecm29 proteasome adaptor and scaffold gene MP:0010733 abnormal axon initial segment morphology IAGP N RGD:5509061 20200213 MGI PMID:31910261 1314599 Ecpas Ecm29 proteasome adaptor and scaffold gene MP:0011987 abnormal GABAergic neuron physiology IAGP N RGD:5509061 20200213 MGI PMID:31910261 1314599 Ecpas Ecm29 proteasome adaptor and scaffold gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210520 MGI 1314600 Nkx2-6 NK2 homeobox 6 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:11390666 1314600 Nkx2-6 NK2 homeobox 6 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11390666 1314600 Nkx2-6 NK2 homeobox 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10733590 1314600 Nkx2-6 NK2 homeobox 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11390666 1314600 Nkx2-6 NK2 homeobox 6 gene MP:0002234 abnormal pharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:11390666 1314600 Nkx2-6 NK2 homeobox 6 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220519 MGI 1314600 Nkx2-6 NK2 homeobox 6 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:11390666 1314600 Nkx2-6 NK2 homeobox 6 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11390666 1314600 Nkx2-6 NK2 homeobox 6 gene MP:0004555 pharynx hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11390666 1314600 Nkx2-6 NK2 homeobox 6 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:11390666 1314600 Nkx2-6 NK2 homeobox 6 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20220519 MGI 1314600 Nkx2-6 NK2 homeobox 6 gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20141003 MGI PMID:11390666 1314600 Nkx2-6 NK2 homeobox 6 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11390666 1314600 Nkx2-6 NK2 homeobox 6 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:11390666 1314600 Nkx2-6 NK2 homeobox 6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11390666 1314602 Atp10a ATPase, class V, type 10A gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20231207 MGI 1314602 Atp10a ATPase, class V, type 10A gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20240523 MGI 1314602 Atp10a ATPase, class V, type 10A gene MP:0001925 male infertility IEA N RGD:5509061 20240523 MGI 1314602 Atp10a ATPase, class V, type 10A gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1314602 Atp10a ATPase, class V, type 10A gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1314603 Fam234b family with sequence similarity 234, member B gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 1314603 Fam234b family with sequence similarity 234, member B gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20160804 MGI 1314603 Fam234b family with sequence similarity 234, member B gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1314603 Fam234b family with sequence similarity 234, member B gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1314603 Fam234b family with sequence similarity 234, member B gene MP:0005571 decreased lactate dehydrogenase level IEA N RGD:5509061 20160804 MGI 1314603 Fam234b family with sequence similarity 234, member B gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20160804 MGI 1314605 Abhd12 abhydrolase domain containing 12 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:23297193 1314605 Abhd12 abhydrolase domain containing 12 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:23297193 1314605 Abhd12 abhydrolase domain containing 12 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23297193 1314605 Abhd12 abhydrolase domain containing 12 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23297193 1314605 Abhd12 abhydrolase domain containing 12 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:23297193 1314605 Abhd12 abhydrolase domain containing 12 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:23297193 1314605 Abhd12 abhydrolase domain containing 12 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:23297193 1314605 Abhd12 abhydrolase domain containing 12 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:23297193 1314605 Abhd12 abhydrolase domain containing 12 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23297193 1314605 Abhd12 abhydrolase domain containing 12 gene MP:0011579 decreased lipoprotein lipase activity IAGP N RGD:5509061 20141003 MGI PMID:23297193 1314605 Abhd12 abhydrolase domain containing 12 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:23297193 1314606 Tmem231 transmembrane protein 231 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:22179047 1314606 Tmem231 transmembrane protein 231 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:22179047 1314606 Tmem231 transmembrane protein 231 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:22179047 1314606 Tmem231 transmembrane protein 231 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:22179047 1314606 Tmem231 transmembrane protein 231 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22179047 1314606 Tmem231 transmembrane protein 231 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22179047 1314609 Radil Ras association and DIL domains gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 1314609 Radil Ras association and DIL domains gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1314611 Dclre1a DNA cross-link repair 1A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16260620 1314611 Dclre1a DNA cross-link repair 1A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16260620 1314611 Dclre1a DNA cross-link repair 1A gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16260620 1314611 Dclre1a DNA cross-link repair 1A gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16260620 1314611 Dclre1a DNA cross-link repair 1A gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16260620 1314611 Dclre1a DNA cross-link repair 1A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16260620 1314611 Dclre1a DNA cross-link repair 1A gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16260620 1314611 Dclre1a DNA cross-link repair 1A gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:18180189 1314611 Dclre1a DNA cross-link repair 1A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10848582 1314611 Dclre1a DNA cross-link repair 1A gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16260620 1314611 Dclre1a DNA cross-link repair 1A gene MP:0009442 increased ovarian teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16260620 1314611 Dclre1a DNA cross-link repair 1A gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10848582 1314611 Dclre1a DNA cross-link repair 1A gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16260620 1314611 Dclre1a DNA cross-link repair 1A gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:16260620 1314611 Dclre1a DNA cross-link repair 1A gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16260620 1314611 Dclre1a DNA cross-link repair 1A gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18180189 1314611 Dclre1a DNA cross-link repair 1A gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16260620 1314612 Prmt9 protein arginine methyltransferase 9 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1314612 Prmt9 protein arginine methyltransferase 9 gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20220929 MGI PMID:36028484 1314612 Prmt9 protein arginine methyltransferase 9 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1314612 Prmt9 protein arginine methyltransferase 9 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1314612 Prmt9 protein arginine methyltransferase 9 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20220811 MGI 1314612 Prmt9 protein arginine methyltransferase 9 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1314612 Prmt9 protein arginine methyltransferase 9 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20220929 MGI PMID:36028484 1314612 Prmt9 protein arginine methyltransferase 9 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20220929 MGI PMID:36028484 1314612 Prmt9 protein arginine methyltransferase 9 gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 1314614 Hoxb9 homeobox B9 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314614 Hoxb9 homeobox B9 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9013929 1314614 Hoxb9 homeobox B9 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:9013929 1314614 Hoxb9 homeobox B9 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:9892669 1314614 Hoxb9 homeobox B9 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:9013929 1314614 Hoxb9 homeobox B9 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314614 Hoxb9 homeobox B9 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:9892669 1314614 Hoxb9 homeobox B9 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314614 Hoxb9 homeobox B9 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314614 Hoxb9 homeobox B9 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9013929 1314614 Hoxb9 homeobox B9 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314614 Hoxb9 homeobox B9 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314614 Hoxb9 homeobox B9 gene MP:0003344 mammary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9892669 1314614 Hoxb9 homeobox B9 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314614 Hoxb9 homeobox B9 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:9013929 1314614 Hoxb9 homeobox B9 gene MP:0004323 sternum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9013929 1314614 Hoxb9 homeobox B9 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314614 Hoxb9 homeobox B9 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314614 Hoxb9 homeobox B9 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:9013929 1314614 Hoxb9 homeobox B9 gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314614 Hoxb9 homeobox B9 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9013929 1314614 Hoxb9 homeobox B9 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314614 Hoxb9 homeobox B9 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:17626057 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20160811 MGI 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20160811 MGI 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20220519 MGI 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1314616 Atp6v0d1 ATPase, H+ transporting, lysosomal V0 subunit D1 gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20240404 MGI PMID:38505620 1314618 Lrp1b low density lipoprotein-related protein 1B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15082773 1314618 Lrp1b low density lipoprotein-related protein 1B gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20220519 MGI 1314618 Lrp1b low density lipoprotein-related protein 1B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20383322 1314618 Lrp1b low density lipoprotein-related protein 1B gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20383322 1314618 Lrp1b low density lipoprotein-related protein 1B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220519 MGI 1314618 Lrp1b low density lipoprotein-related protein 1B gene MP:0011897 decreased circulating unsaturated transferrin level IEA N RGD:5509061 20230601 MGI 1314618 Lrp1b low density lipoprotein-related protein 1B gene MP:0011939 increased food intake IEA N RGD:5509061 20230601 MGI 1314620 Fkbp11 FK506 binding protein 11 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20111116 MGI 1314620 Fkbp11 FK506 binding protein 11 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1314620 Fkbp11 FK506 binding protein 11 gene MP:0000692 small spleen IEA N RGD:5509061 20210128 MGI 1314620 Fkbp11 FK506 binding protein 11 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1314620 Fkbp11 FK506 binding protein 11 gene MP:0001846 increased inflammatory response IEA N RGD:5509061 20111116 MGI 1314620 Fkbp11 FK506 binding protein 11 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1314620 Fkbp11 FK506 binding protein 11 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20201022 MGI 1314620 Fkbp11 FK506 binding protein 11 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1314620 Fkbp11 FK506 binding protein 11 gene MP:0002461 increased immunoglobulin level IEA N RGD:5509061 20111116 MGI 1314620 Fkbp11 FK506 binding protein 11 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20111116 MGI 1314624 Ephb6 Eph receptor B6 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:21540454 1314624 Ephb6 Eph receptor B6 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:21540454 1314624 Ephb6 Eph receptor B6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12379224 1314624 Ephb6 Eph receptor B6 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21540454 1314624 Ephb6 Eph receptor B6 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15599401 1314624 Ephb6 Eph receptor B6 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:15599401 1314624 Ephb6 Eph receptor B6 gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21540454 1314624 Ephb6 Eph receptor B6 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15599401 1314624 Ephb6 Eph receptor B6 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:15599401 1314624 Ephb6 Eph receptor B6 gene MP:0009325 necrospermia IAGP N RGD:5509061 20141003 MGI PMID:21540454 1314624 Ephb6 Eph receptor B6 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:21540454 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20200514 MGI 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20191024 MGI PMID:30605677 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20191024 MGI PMID:30605677 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20191024 MGI PMID:30605677 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20200514 MGI 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230601 MGI 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0004793 abnormal synaptic vesicle clustering IAGP N RGD:5509061 20240530 MGI PMID:36097267 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20191024 MGI PMID:30605677 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20200514 MGI 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20190516 MGI PMID:20178993 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20240530 MGI PMID:36097267 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20240523 MGI 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0010511 shortened PR interval IEA N RGD:5509061 20211021 MGI 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20190516 MGI PMID:20178993 1314628 Zdhhc5 zinc finger, DHHC domain containing 5 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:24113144 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:24113144 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16111477 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16111477 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:24113144 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:24113144 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:24113144 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:24113144 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:24113144 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14532117 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14532117 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:24113144 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:14532117 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20180517 MGI PMID:28593200 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20180517 MGI PMID:28593200 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20141003 MGI PMID:16111477 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:24113144 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:24113144 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:14532117 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20180517 MGI PMID:29242247 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14532117 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20180517 MGI PMID:29242247 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0008055 increased urine osmolality IAGP N RGD:5509061 20180517 MGI PMID:29242247 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:24113144 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20180517 MGI PMID:28593200 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14532117 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14532117 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16111477 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14532117 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20180517 MGI PMID:29242247 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0011466 increased urine urea nitrogen level IAGP N RGD:5509061 20180517 MGI PMID:29242247 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0011470 increased urine creatinine level IAGP N RGD:5509061 20180517 MGI PMID:29242247 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20180517 MGI PMID:29242247 1314630 Stub1 STIP1 homology and U-Box containing protein 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20141003 MGI PMID:24113144 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0000852 small cerebellum IAGP N RGD:5509061 20180222 MGI PMID:26051944 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20180222 MGI PMID:26051944 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180222 MGI PMID:26051944 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0001265 decreased body size IAGP N RGD:5509061 20180222 MGI PMID:26051944 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0001393 ataxia IAGP N RGD:5509061 20180222 MGI PMID:26051944 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180222 MGI PMID:26051944 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230119 MGI 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0001785 edema IEA N RGD:5509061 20230119 MGI 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0002183 gliosis IAGP N RGD:5509061 20180222 MGI PMID:26051944 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0003717 pallor IEA N RGD:5509061 20230119 MGI 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230119 MGI 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180222 MGI PMID:26051944 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20180222 MGI PMID:26051944 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230119 MGI 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180222 MGI PMID:26051944 1314632 Inpp5a inositol polyphosphate-5-phosphatase A gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20230119 MGI 1314634 Exosc8 exosome component 8 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20240523 MGI 1314634 Exosc8 exosome component 8 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1314634 Exosc8 exosome component 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314634 Exosc8 exosome component 8 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1314634 Exosc8 exosome component 8 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0000091 short premaxilla IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0000445 short snout IAGP N RGD:5509061 20171019 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20200827 MGI PMID:25975270 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20181227 MGI 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0000767 abnormal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0001192 scaly skin IEA N RGD:5509061 20181227 MGI 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20200827 MGI PMID:25975270 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:19056881 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19056881 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19056881 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:19056881 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0002293 long gestation period IAGP N RGD:5509061 20141003 MGI PMID:19056881 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200827 MGI PMID:25975270 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0002681 increased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:19056881 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200827 MGI PMID:25975270 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0003103 liver degeneration IAGP N RGD:5509061 20200827 MGI PMID:25975270 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0004832 enlarged ovary IAGP N RGD:5509061 20141003 MGI PMID:19056881 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:19056881 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:19056881 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200827 MGI PMID:25975270 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:19056881 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20200827 MGI PMID:25975270 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0009895 decreased palatine bone horizontal plate size IAGP N RGD:5509061 20141003 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20200827 MGI PMID:25975270 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0011128 increased tertiary ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:19056881 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20200827 MGI PMID:25975270 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0030189 broad snout IAGP N RGD:5509061 20171019 MGI PMID:17143286 1314637 Tiparp TCDD-inducible poly(ADP-ribose) polymerase gene MP:0030383 small presphenoid bone IAGP N RGD:5509061 20171207 MGI PMID:17143286 1314643 Lhx6 LIM homeobox protein 6 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:17376969 1314643 Lhx6 LIM homeobox protein 6 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17376969 1314643 Lhx6 LIM homeobox protein 6 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:17376969 1314643 Lhx6 LIM homeobox protein 6 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1314643 Lhx6 LIM homeobox protein 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22710612 1314643 Lhx6 LIM homeobox protein 6 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:22710612 1314643 Lhx6 LIM homeobox protein 6 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22710612 1314643 Lhx6 LIM homeobox protein 6 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:22710612 1314643 Lhx6 LIM homeobox protein 6 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17376969 1314643 Lhx6 LIM homeobox protein 6 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22710612 1314643 Lhx6 LIM homeobox protein 6 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23142661 1314643 Lhx6 LIM homeobox protein 6 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17376969 1314643 Lhx6 LIM homeobox protein 6 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:22710612 1314643 Lhx6 LIM homeobox protein 6 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22710612 1314643 Lhx6 LIM homeobox protein 6 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:22710612 1314643 Lhx6 LIM homeobox protein 6 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:22710612 1314643 Lhx6 LIM homeobox protein 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17376969 1314643 Lhx6 LIM homeobox protein 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1314643 Lhx6 LIM homeobox protein 6 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17376969 1314643 Lhx6 LIM homeobox protein 6 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1314643 Lhx6 LIM homeobox protein 6 gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:22710612 1314654 Tmem150b transmembrane protein 150B gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20200514 MGI 1314654 Tmem150b transmembrane protein 150B gene MP:0001284 absent vibrissae IEA N RGD:5509061 20210520 MGI 1314654 Tmem150b transmembrane protein 150B gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201022 MGI 1314654 Tmem150b transmembrane protein 150B gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1314654 Tmem150b transmembrane protein 150B gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20200514 MGI 1314654 Tmem150b transmembrane protein 150B gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1314654 Tmem150b transmembrane protein 150B gene MP:0003068 enlarged kidney IEA N RGD:5509061 20200514 MGI 1314654 Tmem150b transmembrane protein 150B gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20210520 MGI 1314654 Tmem150b transmembrane protein 150B gene MP:0013522 decreased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20210520 MGI 1314654 Tmem150b transmembrane protein 150B gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1314656 Phospho1 phosphatase, orphan 1 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0004371 bowed femur IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0004372 bowed fibula IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0004373 bowed humerus IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0008274 failure of bone ossification IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0009445 osteomalacia IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:20684022 1314656 Phospho1 phosphatase, orphan 1 gene MP:0021184 decreased bone mineral density of humerus IAGP N RGD:5509061 20220915 MGI PMID:20684022 1314661 Pramel13 PRAME like 13 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1314661 Pramel13 PRAME like 13 gene MP:0001147 small testis IAGP N RGD:5509061 20210805 MGI PMID:31729367 1314661 Pramel13 PRAME like 13 gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 1314661 Pramel13 PRAME like 13 gene MP:0001925 male infertility IAGP N RGD:5509061 20210805 MGI PMID:31729367 1314661 Pramel13 PRAME like 13 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1314661 Pramel13 PRAME like 13 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20210805 MGI PMID:31729367 1314661 Pramel13 PRAME like 13 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 1314661 Pramel13 PRAME like 13 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210805 MGI PMID:31729367 1314661 Pramel13 PRAME like 13 gene MP:0005159 azoospermia IAGP N RGD:5509061 20210805 MGI PMID:31729367 1314661 Pramel13 PRAME like 13 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210805 MGI PMID:31729367 1314661 Pramel13 PRAME like 13 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20210805 MGI PMID:31729367 1314663 Ivl involucrin gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1314663 Ivl involucrin gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1314663 Ivl involucrin gene MP:0001891 hydrocephaly IEA N RGD:5509061 20210128 MGI 1314663 Ivl involucrin gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1314663 Ivl involucrin gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210128 MGI 1314663 Ivl involucrin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11038184 1314663 Ivl involucrin gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1314667 Wdr37 WD repeat domain 37 gene MP:0000160 kyphosis IEA N RGD:5509061 20150430 MGI 1314667 Wdr37 WD repeat domain 37 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20141003 MGI 1314667 Wdr37 WD repeat domain 37 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20141003 MGI 1314667 Wdr37 WD repeat domain 37 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1314667 Wdr37 WD repeat domain 37 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1314667 Wdr37 WD repeat domain 37 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1314667 Wdr37 WD repeat domain 37 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20160114 MGI 1314667 Wdr37 WD repeat domain 37 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20170105 MGI 1314667 Wdr37 WD repeat domain 37 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20150430 MGI 1314667 Wdr37 WD repeat domain 37 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20141003 MGI 1314667 Wdr37 WD repeat domain 37 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20150108 MGI 1314675 Eif5a2 eukaryotic translation initiation factor 5A2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170706 MGI PMID:26037925 1314684 Igfbp7 insulin-like growth factor binding protein 7 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20150917 MGI PMID:24505323 1314684 Igfbp7 insulin-like growth factor binding protein 7 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20150917 MGI PMID:24505323 1314684 Igfbp7 insulin-like growth factor binding protein 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150917 MGI PMID:24505323 1314684 Igfbp7 insulin-like growth factor binding protein 7 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20150917 MGI PMID:24505323 1314684 Igfbp7 insulin-like growth factor binding protein 7 gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20150917 MGI PMID:24505323 1314684 Igfbp7 insulin-like growth factor binding protein 7 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20150917 MGI PMID:24505323 1314684 Igfbp7 insulin-like growth factor binding protein 7 gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20150917 MGI PMID:24505323 1314684 Igfbp7 insulin-like growth factor binding protein 7 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20150917 MGI PMID:24505323 1314684 Igfbp7 insulin-like growth factor binding protein 7 gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20150917 MGI PMID:24505323 1314684 Igfbp7 insulin-like growth factor binding protein 7 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20191128 MGI 1314684 Igfbp7 insulin-like growth factor binding protein 7 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20150917 MGI PMID:24505323 1314684 Igfbp7 insulin-like growth factor binding protein 7 gene MP:0012075 impaired mammary gland growth during pregnancy IAGP N RGD:5509061 20150917 MGI PMID:24505323 1314684 Igfbp7 insulin-like growth factor binding protein 7 gene MP:0013782 abnormal mammary duct terminal end bud morphology IAGP N RGD:5509061 20150917 MGI PMID:24505323 1314688 Serpinb1a serine (or cysteine) peptidase inhibitor, clade B, member 1a gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17664292 1314688 Serpinb1a serine (or cysteine) peptidase inhibitor, clade B, member 1a gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17664292 1314688 Serpinb1a serine (or cysteine) peptidase inhibitor, clade B, member 1a gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17664292 1314688 Serpinb1a serine (or cysteine) peptidase inhibitor, clade B, member 1a gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17664292 1314688 Serpinb1a serine (or cysteine) peptidase inhibitor, clade B, member 1a gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20141003 MGI PMID:17664292 1314688 Serpinb1a serine (or cysteine) peptidase inhibitor, clade B, member 1a gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:17664292 1314688 Serpinb1a serine (or cysteine) peptidase inhibitor, clade B, member 1a gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20160225 MGI PMID:25180606 1314688 Serpinb1a serine (or cysteine) peptidase inhibitor, clade B, member 1a gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17664292 1314688 Serpinb1a serine (or cysteine) peptidase inhibitor, clade B, member 1a gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:17664292 1314688 Serpinb1a serine (or cysteine) peptidase inhibitor, clade B, member 1a gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17664292 1314688 Serpinb1a serine (or cysteine) peptidase inhibitor, clade B, member 1a gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17664292 1314688 Serpinb1a serine (or cysteine) peptidase inhibitor, clade B, member 1a gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17664292 1314688 Serpinb1a serine (or cysteine) peptidase inhibitor, clade B, member 1a gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:17664292 1314690 Pde6d phosphodiesterase 6D, cGMP-specific, rod, delta gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20160204 MGI PMID:17496142 1314690 Pde6d phosphodiesterase 6D, cGMP-specific, rod, delta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160204 MGI PMID:17496142 1314690 Pde6d phosphodiesterase 6D, cGMP-specific, rod, delta gene MP:0001326 retina degeneration IAGP N RGD:5509061 20160204 MGI PMID:17496142 1314690 Pde6d phosphodiesterase 6D, cGMP-specific, rod, delta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160204 MGI PMID:17496142 1314690 Pde6d phosphodiesterase 6D, cGMP-specific, rod, delta gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20160204 MGI PMID:17496142 1314690 Pde6d phosphodiesterase 6D, cGMP-specific, rod, delta gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20160204 MGI PMID:17496142 1314690 Pde6d phosphodiesterase 6D, cGMP-specific, rod, delta gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20160204 MGI PMID:17496142 1314690 Pde6d phosphodiesterase 6D, cGMP-specific, rod, delta gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20160204 MGI PMID:17496142 1314690 Pde6d phosphodiesterase 6D, cGMP-specific, rod, delta gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20160204 MGI PMID:17496142 1314690 Pde6d phosphodiesterase 6D, cGMP-specific, rod, delta gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:17496142 1314692 Fzd7 frizzled class receptor 7 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314692 Fzd7 frizzled class receptor 7 gene MP:0011203 abnormal parietal yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:23095888 1314693 Kif21b kinesin family member 21B gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1314693 Kif21b kinesin family member 21B gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160804 MGI 1314693 Kif21b kinesin family member 21B gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160804 MGI 1314693 Kif21b kinesin family member 21B gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 1314693 Kif21b kinesin family member 21B gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20180125 MGI PMID:27117409 1314693 Kif21b kinesin family member 21B gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20180125 MGI PMID:27117409 1314693 Kif21b kinesin family member 21B gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20180125 MGI PMID:27117409 1314693 Kif21b kinesin family member 21B gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20180125 MGI PMID:27117409 1314693 Kif21b kinesin family member 21B gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20180125 MGI PMID:27117409 1314693 Kif21b kinesin family member 21B gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20180125 MGI PMID:27117409 1314696 Lkaaear1 LKAAEAR motif containing 1 (IKAAEAR murine motif) gene MP:0000745 tremors IEA N RGD:5509061 20240523 MGI 1314697 Zfp746 zinc finger protein 746 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220519 MGI 1314697 Zfp746 zinc finger protein 746 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20241114 MGI PMID:31237944 1314697 Zfp746 zinc finger protein 746 gene MP:0001661 extended life span IAGP N RGD:5509061 20241114 MGI PMID:31237944 1314697 Zfp746 zinc finger protein 746 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1314697 Zfp746 zinc finger protein 746 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20241114 MGI PMID:31237944 1314697 Zfp746 zinc finger protein 746 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20241114 MGI PMID:31237944 1314697 Zfp746 zinc finger protein 746 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20240523 MGI 1314697 Zfp746 zinc finger protein 746 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220519 MGI 1314697 Zfp746 zinc finger protein 746 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1314697 Zfp746 zinc finger protein 746 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20240314 MGI PMID:34062393 1314697 Zfp746 zinc finger protein 746 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220519 MGI 1314697 Zfp746 zinc finger protein 746 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1314697 Zfp746 zinc finger protein 746 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20240523 MGI 1314699 Spin1 spindlin 1 gene MP:0000161 scoliosis IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 1314699 Spin1 spindlin 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1314699 Spin1 spindlin 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1314699 Spin1 spindlin 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1314699 Spin1 spindlin 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1314699 Spin1 spindlin 1 gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0004094 abnormal M line morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20181227 MGI 1314699 Spin1 spindlin 1 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20141003 MGI PMID:23894536 1314699 Spin1 spindlin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23894536 1314699 Spin1 spindlin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20210401 MGI PMID:29168801 1314699 Spin1 spindlin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000192 abnormal mineral level IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:7579418 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20201022 MGI 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000414 alopecia IEA N RGD:5509061 20111116 MGI 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:1325193 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000472 abnormal stomach non-glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:1325193 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:7650236 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000580 deformed nails IAGP N RGD:5509061 20141003 MGI PMID:7650236 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:7579418 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7579418 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:7579418 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7579418 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001195 flaky skin IEA N RGD:5509061 20111116 MGI 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001212 skin lesions IEA N RGD:5509061 20111116 MGI 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7650236 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:7650236 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20171012 MGI PMID:8406628 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001220 epidermal necrosis IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001239 abnormal epidermis stratum granulosum morphology IEA N RGD:5509061 20111116 MGI 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001243 abnormal dermal layer morphology IEA N RGD:5509061 20111116 MGI 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7579418 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:1325193 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001586 abnormal erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001586 abnormal erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:1325193 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:1325193 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7650236 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:7650236 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20170921 MGI PMID:7650236 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20200402 MGI 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0004152 abnormal circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0005096 erythroblastosis IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0005096 erythroblastosis IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0005174 abnormal tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:15155459 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0009600 hypergranulosis IAGP N RGD:5509061 20141003 MGI PMID:7650236 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0009602 abnormal keratohyalin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:7650236 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0009675 orthokeratosis IEA N RGD:5509061 20111116 MGI 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20200402 MGI 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0010176 dacryocytosis IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0010177 acanthocytosis IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0010784 abnormal forestomach morphology IAGP N RGD:5509061 20141003 MGI PMID:1325193 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:1325193 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0011242 increased fetal derived definitive erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16093647 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0011413 colorless urine IAGP N RGD:5509061 20141003 MGI PMID:6678340 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0013409 increased dendritic epidermal T cell number IAGP N RGD:5509061 20171012 MGI PMID:8406628 1314701 Ttc7 tetratricopeptide repeat domain 7 gene MP:0013412 increased Langerhans cell number IAGP N RGD:5509061 20171012 MGI PMID:8406628 1314704 Pak6 p21 (RAC1) activated kinase 6 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18675265 1314704 Pak6 p21 (RAC1) activated kinase 6 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:18675265 1314704 Pak6 p21 (RAC1) activated kinase 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18675265 1314704 Pak6 p21 (RAC1) activated kinase 6 gene MP:0002798 abnormal active avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:18675265 1314704 Pak6 p21 (RAC1) activated kinase 6 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18675265 1314704 Pak6 p21 (RAC1) activated kinase 6 gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:18675265 1314704 Pak6 p21 (RAC1) activated kinase 6 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:18675265 1314704 Pak6 p21 (RAC1) activated kinase 6 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:18675265 1314704 Pak6 p21 (RAC1) activated kinase 6 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:18675265 1314704 Pak6 p21 (RAC1) activated kinase 6 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1314704 Pak6 p21 (RAC1) activated kinase 6 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20201231 MGI 1314705 Csrnp3 cysteine-serine-rich nuclear protein 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17726538 1314705 Csrnp3 cysteine-serine-rich nuclear protein 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17726538 1314706 Paxx non-homologous end joining factor gene MP:0000692 small spleen IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1314706 Paxx non-homologous end joining factor gene MP:0000705 athymia IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0000726 absent lymphocyte IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1314706 Paxx non-homologous end joining factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1314706 Paxx non-homologous end joining factor gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20170413 MGI PMID:27798842 1314706 Paxx non-homologous end joining factor gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20240523 MGI 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20141003 MGI 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:18693278 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:18693278 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18693278 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22972987 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:18693278 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0004113 abnormal aortic arch morphology IEA N RGD:5509061 20141003 MGI 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141003 MGI 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18693278 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12464436 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0011659 interrupted aortic arch, type b IEA N RGD:5509061 20231214 MGI 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0011662 persistent truncus arteriosus type ii IEA N RGD:5509061 20231228 MGI 1314708 Tab1 TGF-beta activated kinase 1/MAP3K7 binding protein 1 gene MP:0011676 aortic arch obstruction IEA N RGD:5509061 20231228 MGI 1314710 Pcp2 Purkinje cell protein 2 (L7) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17270300 1314710 Pcp2 Purkinje cell protein 2 (L7) gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:17270300 1314710 Pcp2 Purkinje cell protein 2 (L7) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15883005 1314710 Pcp2 Purkinje cell protein 2 (L7) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9191112 1314710 Pcp2 Purkinje cell protein 2 (L7) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9204480 1314710 Pcp2 Purkinje cell protein 2 (L7) gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17270300 1314718 Aqr aquarius gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12904583 1314718 Aqr aquarius gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8643689 1314718 Aqr aquarius gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9626505 1314720 Gtsf1l gametocyte specific factor 1-like gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1314720 Gtsf1l gametocyte specific factor 1-like gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1314722 Tprg1 transformation related protein 63 regulated 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20231207 MGI 1314722 Tprg1 transformation related protein 63 regulated 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 1314722 Tprg1 transformation related protein 63 regulated 1 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20231207 MGI 1314722 Tprg1 transformation related protein 63 regulated 1 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20231207 MGI 1314722 Tprg1 transformation related protein 63 regulated 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1314723 4833420G17Rik RIKEN cDNA 4833420G17 gene gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1314723 4833420G17Rik RIKEN cDNA 4833420G17 gene gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1314723 4833420G17Rik RIKEN cDNA 4833420G17 gene gene MP:0001258 decreased body length IEA N RGD:5509061 20230601 MGI 1314723 4833420G17Rik RIKEN cDNA 4833420G17 gene gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1314723 4833420G17Rik RIKEN cDNA 4833420G17 gene gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220519 MGI 1314726 Setbp1 SET binding protein 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20210826 MGI 1314726 Setbp1 SET binding protein 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20170105 MGI 1314726 Setbp1 SET binding protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1314727 Henmt1 HEN1 methyltransferase homolog 1 (Arabidopsis) gene MP:0001925 male infertility IAGP N RGD:5509061 20171109 MGI PMID:26496356 1314727 Henmt1 HEN1 methyltransferase homolog 1 (Arabidopsis) gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20171109 MGI PMID:26496356 1314727 Henmt1 HEN1 methyltransferase homolog 1 (Arabidopsis) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20171109 MGI PMID:26496356 1314727 Henmt1 HEN1 methyltransferase homolog 1 (Arabidopsis) gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20171109 MGI PMID:26496356 1314727 Henmt1 HEN1 methyltransferase homolog 1 (Arabidopsis) gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20171109 MGI PMID:26496356 1314727 Henmt1 HEN1 methyltransferase homolog 1 (Arabidopsis) gene MP:0008261 arrest of male meiosis IEA N RGD:5509061 20220721 MGI 1314727 Henmt1 HEN1 methyltransferase homolog 1 (Arabidopsis) gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20171109 MGI PMID:26496356 1314727 Henmt1 HEN1 methyltransferase homolog 1 (Arabidopsis) gene MP:0009236 pinhead sperm IAGP N RGD:5509061 20171109 MGI PMID:26496356 1314727 Henmt1 HEN1 methyltransferase homolog 1 (Arabidopsis) gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20171109 MGI PMID:26496356 1314727 Henmt1 HEN1 methyltransferase homolog 1 (Arabidopsis) gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20171109 MGI PMID:26496356 1314727 Henmt1 HEN1 methyltransferase homolog 1 (Arabidopsis) gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20171109 MGI PMID:26496356 1314729 Rwdd2a RWD domain containing 2A gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230105 MGI 1314729 Rwdd2a RWD domain containing 2A gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20230105 MGI 1314729 Rwdd2a RWD domain containing 2A gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1314729 Rwdd2a RWD domain containing 2A gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230105 MGI 1314729 Rwdd2a RWD domain containing 2A gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1314729 Rwdd2a RWD domain containing 2A gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230105 MGI 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0000650 mesocardia IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20220120 MGI PMID:34715025 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170504 MGI 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0002766 situs inversus IAGP N RGD:5509061 20220120 MGI PMID:34715025 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0002767 situs ambiguus IAGP N RGD:5509061 20220120 MGI PMID:34715025 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0008933 abnormal motile primary cilium physiology IAGP N RGD:5509061 20220120 MGI PMID:34715025 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0008987 abnormal liver lobule morphology IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230720 MGI 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0010595 abnormal aortic valve cusp morphology IEA N RGD:5509061 20170504 MGI 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0010853 abnormal lung position or orientation IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20220120 MGI PMID:34715025 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20220120 MGI PMID:34715025 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20220120 MGI PMID:34715025 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0011252 situs inversus totalis IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0013847 retropleural edema IEA N RGD:5509061 20170504 MGI 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1314732 Pierce1 piercer of microtubule wall 1 gene MP:0020494 left sided inferior vena cava IAGP N RGD:5509061 20180222 MGI PMID:27305836 1314739 Kctd7 potassium channel tetramerisation domain containing 7 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20190711 MGI 1314739 Kctd7 potassium channel tetramerisation domain containing 7 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1314739 Kctd7 potassium channel tetramerisation domain containing 7 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230601 MGI 1314739 Kctd7 potassium channel tetramerisation domain containing 7 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1314760 Krt33a keratin 33A gene MP:0000411 shiny fur IEA N RGD:5509061 20111116 MGI 1314760 Krt33a keratin 33A gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1314760 Krt33a keratin 33A gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1314760 Krt33a keratin 33A gene MP:0001511 disheveled coat IEA N RGD:5509061 20111116 MGI 1314760 Krt33a keratin 33A gene MP:0003849 greasy coat IEA N RGD:5509061 20111116 MGI 1314760 Krt33a keratin 33A gene MP:0011047 increased lung tissue damping IEA N RGD:5509061 20211021 MGI 1314764 Elavl2 ELAV like RNA binding protein 1 gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20231207 MGI 1314764 Elavl2 ELAV like RNA binding protein 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20230928 MGI PMID:31657143 1314764 Elavl2 ELAV like RNA binding protein 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20230928 MGI PMID:31657143 1314764 Elavl2 ELAV like RNA binding protein 1 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20240523 MGI 1314764 Elavl2 ELAV like RNA binding protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230928 MGI PMID:31657143 1314764 Elavl2 ELAV like RNA binding protein 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20230928 MGI PMID:31657143 1314764 Elavl2 ELAV like RNA binding protein 1 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20230928 MGI PMID:31657143 1314764 Elavl2 ELAV like RNA binding protein 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20230928 MGI PMID:31657143 1314764 Elavl2 ELAV like RNA binding protein 1 gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20230928 MGI PMID:31657143 1314764 Elavl2 ELAV like RNA binding protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20230928 MGI PMID:31657143 1314764 Elavl2 ELAV like RNA binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1314764 Elavl2 ELAV like RNA binding protein 1 gene MP:0011122 absent primordial ovarian follicles IAGP N RGD:5509061 20230928 MGI PMID:31657143 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20201022 MGI 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:22832496 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:22832496 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22832496 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:22832496 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:22832496 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20201022 MGI 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:22832496 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0009597 impaired stratum corneum desquamation IAGP N RGD:5509061 20141003 MGI PMID:22832496 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22832496 1314766 Aloxe3 arachidonate lipoxygenase 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314770 Ap2a1 adaptor-related protein complex 2, alpha 1 subunit gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1314770 Ap2a1 adaptor-related protein complex 2, alpha 1 subunit gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1314770 Ap2a1 adaptor-related protein complex 2, alpha 1 subunit gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1314770 Ap2a1 adaptor-related protein complex 2, alpha 1 subunit gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1314770 Ap2a1 adaptor-related protein complex 2, alpha 1 subunit gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20220811 MGI 1314770 Ap2a1 adaptor-related protein complex 2, alpha 1 subunit gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1314770 Ap2a1 adaptor-related protein complex 2, alpha 1 subunit gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1314770 Ap2a1 adaptor-related protein complex 2, alpha 1 subunit gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0001722 pale yolk sac IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0001785 edema IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0002861 abnormal tail bud morphology IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20240523 MGI 1314771 Sass6 SAS-6 centriolar assembly protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1314776 Clca1 chloride channel accessory 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16645179 1314776 Clca1 chloride channel accessory 1 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1314776 Clca1 chloride channel accessory 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15947424 1314776 Clca1 chloride channel accessory 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16645179 1314776 Clca1 chloride channel accessory 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:16645179 1314776 Clca1 chloride channel accessory 1 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20210128 MGI 1314776 Clca1 chloride channel accessory 1 gene MP:0002281 abnormal respiratory mucosa goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16645179 1314776 Clca1 chloride channel accessory 1 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16645179 1314776 Clca1 chloride channel accessory 1 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:16645179 1314776 Clca1 chloride channel accessory 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1314776 Clca1 chloride channel accessory 1 gene MP:0010936 decreased airway resistance IAGP N RGD:5509061 20141003 MGI PMID:16645179 1314781 Btbd7 BTB domain containing 7 gene MP:0000162 lordosis IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0002311 abnormal inspiratory capacity IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20181227 MGI PMID:28506999 1314781 Btbd7 BTB domain containing 7 gene MP:0009520 decreased submandibular gland size IAGP N RGD:5509061 20181227 MGI PMID:28506999 1314781 Btbd7 BTB domain containing 7 gene MP:0009709 hydrometra IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20181227 MGI PMID:28506999 1314781 Btbd7 BTB domain containing 7 gene MP:0010895 increased lung compliance IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20181227 MGI PMID:28506999 1314781 Btbd7 BTB domain containing 7 gene MP:0011045 decreased lung elastance IEA N RGD:5509061 20230119 MGI 1314781 Btbd7 BTB domain containing 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20181227 MGI PMID:28506999 1314781 Btbd7 BTB domain containing 7 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20181227 MGI PMID:28506999 1314781 Btbd7 BTB domain containing 7 gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20181227 MGI PMID:28506999 1314781 Btbd7 BTB domain containing 7 gene MP:0013541 abnormal submandibular gland development IAGP N RGD:5509061 20181227 MGI PMID:28506999 1314781 Btbd7 BTB domain containing 7 gene MP:0013542 abnormal submandibular gland branching morphogenesis IAGP N RGD:5509061 20181227 MGI PMID:28506999 1314783 Slamf8 SLAM family member 8 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:22593622 1314783 Slamf8 SLAM family member 8 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:22593622 1314785 Zfp763 zinc finger protein 763 gene MP:0003443 increased circulating glycerol level IEA N RGD:5509061 20211021 MGI 1314787 Capza1 capping actin protein of muscle Z-line subunit alpha 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230119 MGI 1314787 Capza1 capping actin protein of muscle Z-line subunit alpha 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20230119 MGI 1314787 Capza1 capping actin protein of muscle Z-line subunit alpha 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230119 MGI 1314787 Capza1 capping actin protein of muscle Z-line subunit alpha 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1314787 Capza1 capping actin protein of muscle Z-line subunit alpha 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1314787 Capza1 capping actin protein of muscle Z-line subunit alpha 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20230119 MGI 1314787 Capza1 capping actin protein of muscle Z-line subunit alpha 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1314787 Capza1 capping actin protein of muscle Z-line subunit alpha 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 1314787 Capza1 capping actin protein of muscle Z-line subunit alpha 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230119 MGI 1314787 Capza1 capping actin protein of muscle Z-line subunit alpha 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20230119 MGI 1314787 Capza1 capping actin protein of muscle Z-line subunit alpha 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20230119 MGI 1314787 Capza1 capping actin protein of muscle Z-line subunit alpha 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230119 MGI 1314787 Capza1 capping actin protein of muscle Z-line subunit alpha 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230119 MGI 1314793 Sipa1l2 signal-induced proliferation-associated 1 like 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20200730 MGI PMID:31784514 1314793 Sipa1l2 signal-induced proliferation-associated 1 like 2 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20200730 MGI PMID:31784514 1314794 Acad11 acyl-Coenzyme A dehydrogenase family, member 11 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1314794 Acad11 acyl-Coenzyme A dehydrogenase family, member 11 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1314794 Acad11 acyl-Coenzyme A dehydrogenase family, member 11 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20211021 MGI 1314795 D630045J12Rik RIKEN cDNA D630045J12 gene gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20160811 MGI 1314795 D630045J12Rik RIKEN cDNA D630045J12 gene gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 1314795 D630045J12Rik RIKEN cDNA D630045J12 gene gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1314795 D630045J12Rik RIKEN cDNA D630045J12 gene gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20170105 MGI 1314795 D630045J12Rik RIKEN cDNA D630045J12 gene gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20190502 MGI 1314795 D630045J12Rik RIKEN cDNA D630045J12 gene gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1314795 D630045J12Rik RIKEN cDNA D630045J12 gene gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1314795 D630045J12Rik RIKEN cDNA D630045J12 gene gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1314797 Spic Spi-C transcription factor (Spi-1/PU.1 related) gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:19037245 1314797 Spic Spi-C transcription factor (Spi-1/PU.1 related) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24630724 1314797 Spic Spi-C transcription factor (Spi-1/PU.1 related) gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:19037245 1314797 Spic Spi-C transcription factor (Spi-1/PU.1 related) gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:24630724 1314797 Spic Spi-C transcription factor (Spi-1/PU.1 related) gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19037245 1314797 Spic Spi-C transcription factor (Spi-1/PU.1 related) gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:19037245 1314797 Spic Spi-C transcription factor (Spi-1/PU.1 related) gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19037245 1314799 Fer FER tyrosine kinase gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1314799 Fer FER tyrosine kinase gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201022 MGI 1314799 Fer FER tyrosine kinase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1314799 Fer FER tyrosine kinase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1314799 Fer FER tyrosine kinase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1314799 Fer FER tyrosine kinase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20221215 MGI 1314799 Fer FER tyrosine kinase gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1314799 Fer FER tyrosine kinase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1314799 Fer FER tyrosine kinase gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220519 MGI 1314799 Fer FER tyrosine kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11134346 1314799 Fer FER tyrosine kinase gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 1314799 Fer FER tyrosine kinase gene MP:0002989 small kidney IEA N RGD:5509061 20220519 MGI 1314799 Fer FER tyrosine kinase gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1314799 Fer FER tyrosine kinase gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 1314799 Fer FER tyrosine kinase gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1314799 Fer FER tyrosine kinase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201022 MGI 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16148091 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16148091 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:16148091 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:16148091 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16148091 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16148091 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20171116 MGI PMID:26683084 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0008168 decreased B-1a cell number IEA N RGD:5509061 20190110 MGI 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0008170 decreased B-1b cell number IEA N RGD:5509061 20190110 MGI 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:16148091 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16148091 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0008191 abnormal follicular B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16148091 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20171116 MGI PMID:26683084 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20171116 MGI PMID:26683084 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0020335 abnormal dentate gyrus neuron dendrite morphology IAGP N RGD:5509061 20171116 MGI PMID:26683084 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20211014 MGI PMID:26683084 1314804 Nedd9 neural precursor cell expressed, developmentally down-regulated gene 9 gene MP:0020916 increased susceptibility to Herpesvirales infection IEA N RGD:5509061 20200430 MGI 1314807 Zfp282 zinc finger protein 282 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240822 MGI PMID:38050179 1314809 Abr active BCR-related gene gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:11921339 1314809 Abr active BCR-related gene gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:11684658 1314809 Abr active BCR-related gene gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:11684658 1314809 Abr active BCR-related gene gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11684658 1314809 Abr active BCR-related gene gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11684658 1314809 Abr active BCR-related gene gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11921339 1314809 Abr active BCR-related gene gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11684658 1314809 Abr active BCR-related gene gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11921339 1314809 Abr active BCR-related gene gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11684658 1314809 Abr active BCR-related gene gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11921339 1314809 Abr active BCR-related gene gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:11921339 1314809 Abr active BCR-related gene gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11921339 1314809 Abr active BCR-related gene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11684658 1314809 Abr active BCR-related gene gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11684658 1314809 Abr active BCR-related gene gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:11684658 1314809 Abr active BCR-related gene gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:11684658 1314809 Abr active BCR-related gene gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:11684658 1314809 Abr active BCR-related gene gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:11921339 1314809 Abr active BCR-related gene gene MP:0003143 enlarged otoliths IAGP N RGD:5509061 20141003 MGI PMID:11921339 1314809 Abr active BCR-related gene gene MP:0003144 decreased otolith number IAGP N RGD:5509061 20141003 MGI PMID:11921339 1314809 Abr active BCR-related gene gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11684658 1314809 Abr active BCR-related gene gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:11921339 1314809 Abr active BCR-related gene gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11921339 1314809 Abr active BCR-related gene gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11684658 1314809 Abr active BCR-related gene gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11684658 1314809 Abr active BCR-related gene gene MP:0011238 abnormal inner ear development IAGP N RGD:5509061 20240822 MGI PMID:11921339 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:15199142 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:15199142 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:15199142 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15199142 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0001717 absent ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:15199142 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20170216 MGI PMID:27068806 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:15199142 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15199142 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20170216 MGI PMID:27068806 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20170216 MGI PMID:27068806 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20170216 MGI PMID:27068806 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20170216 MGI PMID:27068806 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0010040 abnormal oval cell morphology IAGP N RGD:5509061 20170216 MGI PMID:27068806 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0010042 abnormal oval cell physiology IAGP N RGD:5509061 20170216 MGI PMID:27068806 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15199142 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15199142 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0011197 abnormal proamniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:15199142 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0011198 absent proamniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:15199142 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0011208 small proamniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:15199142 1314811 Ppp1r8 protein phosphatase 1, regulatory subunit 8 gene MP:0014233 bile duct epithelium hyperplasia IAGP N RGD:5509061 20170216 MGI PMID:27068806 1314813 Aamp angio-associated migratory protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1314813 Aamp angio-associated migratory protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1314816 Ndufa8 NADH:ubiquinone oxidoreductase subunit A8 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20220811 MGI 1314816 Ndufa8 NADH:ubiquinone oxidoreductase subunit A8 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1314816 Ndufa8 NADH:ubiquinone oxidoreductase subunit A8 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20220811 MGI 1314816 Ndufa8 NADH:ubiquinone oxidoreductase subunit A8 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20160804 MGI 1314816 Ndufa8 NADH:ubiquinone oxidoreductase subunit A8 gene MP:0010052 increased grip strength IEA N RGD:5509061 20160804 MGI 1314816 Ndufa8 NADH:ubiquinone oxidoreductase subunit A8 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1314816 Ndufa8 NADH:ubiquinone oxidoreductase subunit A8 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1314816 Ndufa8 NADH:ubiquinone oxidoreductase subunit A8 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220811 MGI 1314816 Ndufa8 NADH:ubiquinone oxidoreductase subunit A8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314816 Ndufa8 NADH:ubiquinone oxidoreductase subunit A8 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20160421 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20230601 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20221215 MGI PMID:36099048 1314817 Mettl23 methyltransferase like 23 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230601 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230601 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230601 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20230316 MGI PMID:28930672 1314817 Mettl23 methyltransferase like 23 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230601 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0002981 increased liver weight IEA N RGD:5509061 20240523 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20221215 MGI PMID:36099048 1314817 Mettl23 methyltransferase like 23 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230601 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0005391 vision/eye phenotype IAGP N RGD:5509061 20221215 MGI PMID:36099048 1314817 Mettl23 methyltransferase like 23 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20221215 MGI PMID:36099048 1314817 Mettl23 methyltransferase like 23 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20230601 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20221215 MGI PMID:36099048 1314817 Mettl23 methyltransferase like 23 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20230316 MGI PMID:28930672 1314817 Mettl23 methyltransferase like 23 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20230316 MGI PMID:28930672 1314817 Mettl23 methyltransferase like 23 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20230316 MGI PMID:28930672 1314817 Mettl23 methyltransferase like 23 gene MP:0011496 abnormal head size IEA N RGD:5509061 20230601 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0011896 increased circulating unsaturated transferrin level IEA N RGD:5509061 20230601 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20230601 MGI 1314817 Mettl23 methyltransferase like 23 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1314819 Vav2 vav 2 oncogene gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19139088 1314819 Vav2 vav 2 oncogene gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:19139088 1314819 Vav2 vav 2 oncogene gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15848800 1314819 Vav2 vav 2 oncogene gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:19139088 1314819 Vav2 vav 2 oncogene gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11376342 1314819 Vav2 vav 2 oncogene gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:20140222 1314819 Vav2 vav 2 oncogene gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17158234 1314819 Vav2 vav 2 oncogene gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17158234 1314819 Vav2 vav 2 oncogene gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15848800 1314819 Vav2 vav 2 oncogene gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0003184 increased angiotensin I-converting enzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:16782872 1314819 Vav2 vav 2 oncogene gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:16782872 1314819 Vav2 vav 2 oncogene gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16782872 1314819 Vav2 vav 2 oncogene gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:20140222 1314819 Vav2 vav 2 oncogene gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:11376342 1314819 Vav2 vav 2 oncogene gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11376342 1314819 Vav2 vav 2 oncogene gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11376342 1314819 Vav2 vav 2 oncogene gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20141003 MGI PMID:20140222 1314819 Vav2 vav 2 oncogene gene MP:0005489 vascular smooth muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0005497 optic nerve cupping IAGP N RGD:5509061 20141003 MGI PMID:20140222 1314819 Vav2 vav 2 oncogene gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0005582 increased renin activity IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16782872 1314819 Vav2 vav 2 oncogene gene MP:0005610 increased circulating antidiuretic hormone level IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0005662 increased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0005665 increased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:20140222 1314819 Vav2 vav 2 oncogene gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11376342 1314819 Vav2 vav 2 oncogene gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11376342 1314819 Vav2 vav 2 oncogene gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:11376342 1314819 Vav2 vav 2 oncogene gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11376342 1314819 Vav2 vav 2 oncogene gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11376342 1314819 Vav2 vav 2 oncogene gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0008300 enlarged adrenal medulla IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0008301 adrenal medulla hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:11376342 1314819 Vav2 vav 2 oncogene gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11376342 1314819 Vav2 vav 2 oncogene gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:11376342 1314819 Vav2 vav 2 oncogene gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11376342 1314819 Vav2 vav 2 oncogene gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17158234 1314819 Vav2 vav 2 oncogene gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:17158234 1314819 Vav2 vav 2 oncogene gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:11376343 1314819 Vav2 vav 2 oncogene gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20140222 1314819 Vav2 vav 2 oncogene gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20140222 1314819 Vav2 vav 2 oncogene gene MP:0009274 buphthalmos IAGP N RGD:5509061 20141003 MGI PMID:20140222 1314819 Vav2 vav 2 oncogene gene MP:0009812 abnormal bradykinin level IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:17202406 1314819 Vav2 vav 2 oncogene gene MP:0009922 increased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1314819 Vav2 vav 2 oncogene gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22683124 1314819 Vav2 vav 2 oncogene gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20150430 MGI PMID:20140222 1314819 Vav2 vav 2 oncogene gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:11376342 1314819 Vav2 vav 2 oncogene gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:14623913 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20230601 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0000745 tremors IEA N RGD:5509061 20190404 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0001394 circling IEA N RGD:5509061 20190404 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0001406 abnormal gait IEA N RGD:5509061 20210128 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0001443 poor grooming IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210128 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0002083 premature death IAGP N RGD:5509061 20200206 MGI PMID:27715390 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0002626 increased heart rate IEA N RGD:5509061 20230601 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0002764 short tibia IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200206 MGI PMID:27715390 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20200206 MGI PMID:27715390 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20200206 MGI PMID:27715390 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200206 MGI PMID:27715390 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20200206 MGI PMID:27715390 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200206 MGI PMID:27715390 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200206 MGI PMID:27715390 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0009122 decreased white fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0009974 decreased cerebral cortex pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0011975 neuronal cytoplasmic inclusions IAGP N RGD:5509061 20141003 MGI PMID:23479740 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200206 MGI PMID:27715390 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200206 MGI PMID:27715390 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20210826 MGI 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0020811 abnormal photoreceptor outer segment size IAGP N RGD:5509061 20200206 MGI PMID:27715390 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20200206 MGI PMID:27715390 1314820 Epg5 ectopic P-granules 5 autophagy tethering factor gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200206 MGI PMID:27715390 1314821 Zfc3h1 zinc finger, C3H1-type containing gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220811 MGI 1314821 Zfc3h1 zinc finger, C3H1-type containing gene MP:0000601 small liver IEA N RGD:5509061 20220811 MGI 1314821 Zfc3h1 zinc finger, C3H1-type containing gene MP:0001257 increased body length IEA N RGD:5509061 20231207 MGI 1314821 Zfc3h1 zinc finger, C3H1-type containing gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1314821 Zfc3h1 zinc finger, C3H1-type containing gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20231207 MGI 1314821 Zfc3h1 zinc finger, C3H1-type containing gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1314821 Zfc3h1 zinc finger, C3H1-type containing gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1314825 Ivns1abp influenza virus NS1A binding protein gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15485691 1314825 Ivns1abp influenza virus NS1A binding protein gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15485691 1314825 Ivns1abp influenza virus NS1A binding protein gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:15485691 1314825 Ivns1abp influenza virus NS1A binding protein gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15485691 1314825 Ivns1abp influenza virus NS1A binding protein gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:15485691 1314825 Ivns1abp influenza virus NS1A binding protein gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15485691 1314825 Ivns1abp influenza virus NS1A binding protein gene MP:0010334 pleural effusion IAGP N RGD:5509061 20141003 MGI PMID:15485691 1314825 Ivns1abp influenza virus NS1A binding protein gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15485691 1314827 Slc39a2 solute carrier family 39 (zinc transporter), member 2 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:17506078 1314827 Slc39a2 solute carrier family 39 (zinc transporter), member 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:17506078 1314827 Slc39a2 solute carrier family 39 (zinc transporter), member 2 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:17506078 1314827 Slc39a2 solute carrier family 39 (zinc transporter), member 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17506078 1314827 Slc39a2 solute carrier family 39 (zinc transporter), member 2 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17506078 1314827 Slc39a2 solute carrier family 39 (zinc transporter), member 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:17506078 1314827 Slc39a2 solute carrier family 39 (zinc transporter), member 2 gene MP:0008738 abnormal liver iron level IAGP N RGD:5509061 20141003 MGI PMID:17506078 1314829 Trdmt1 tRNA aspartic acid methyltransferase 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1314829 Trdmt1 tRNA aspartic acid methyltransferase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1314829 Trdmt1 tRNA aspartic acid methyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16424344 1314829 Trdmt1 tRNA aspartic acid methyltransferase 1 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20111116 MGI 1314829 Trdmt1 tRNA aspartic acid methyltransferase 1 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 1314829 Trdmt1 tRNA aspartic acid methyltransferase 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1314829 Trdmt1 tRNA aspartic acid methyltransferase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1314831 Skil SKI-like gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12861029 1314831 Skil SKI-like gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12861029 1314831 Skil SKI-like gene MP:0001881 abnormal mammary gland physiology IAGP N RGD:5509061 20161208 MGI PMID:22833129 1314831 Skil SKI-like gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10811619 1314831 Skil SKI-like gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10811619 1314831 Skil SKI-like gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:12861029 1314831 Skil SKI-like gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:10811619 1314831 Skil SKI-like gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:19745809 1314831 Skil SKI-like gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:10811619 1314831 Skil SKI-like gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:19745809 1314831 Skil SKI-like gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12861029 1314831 Skil SKI-like gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10811619 1314831 Skil SKI-like gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20161208 MGI PMID:22833129 1314831 Skil SKI-like gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:19745809 1314831 Skil SKI-like gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20161208 MGI PMID:22833129 1314831 Skil SKI-like gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20161208 MGI PMID:22833129 1314831 Skil SKI-like gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10811619 1314831 Skil SKI-like gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20221215 MGI 1314831 Skil SKI-like gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10811619 1314831 Skil SKI-like gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19745809 1314831 Skil SKI-like gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:19745809 1314831 Skil SKI-like gene MP:0012075 impaired mammary gland growth during pregnancy IAGP N RGD:5509061 20161208 MGI PMID:22833129 1314831 Skil SKI-like gene MP:0013716 hypolactation IAGP N RGD:5509061 20161208 MGI PMID:22833129 1314831 Skil SKI-like gene MP:0013781 abnormal mammary gland luminal epithelium morphology IAGP N RGD:5509061 20161208 MGI PMID:22833129 1314836 Rapsn receptor-associated protein of the synapse gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:7675108 1314836 Rapsn receptor-associated protein of the synapse gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:7675108 1314836 Rapsn receptor-associated protein of the synapse gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20200220 MGI PMID:31549961 1314836 Rapsn receptor-associated protein of the synapse gene MP:0001055 failure of neuromuscular synapse postsynaptic differentiation IAGP N RGD:5509061 20141003 MGI PMID:7675108 1314836 Rapsn receptor-associated protein of the synapse gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1314836 Rapsn receptor-associated protein of the synapse gene MP:0001575 cyanosis IAGP N RGD:5509061 20200220 MGI PMID:31549961 1314836 Rapsn receptor-associated protein of the synapse gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:7675108 1314836 Rapsn receptor-associated protein of the synapse gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20200220 MGI PMID:31549961 1314836 Rapsn receptor-associated protein of the synapse gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20200220 MGI PMID:31549961 1314836 Rapsn receptor-associated protein of the synapse gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200220 MGI PMID:31549961 1314836 Rapsn receptor-associated protein of the synapse gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7675108 1314836 Rapsn receptor-associated protein of the synapse gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314838 Pcdh20 protocadherin 20 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1314838 Pcdh20 protocadherin 20 gene MP:0001410 head bobbing IEA N RGD:5509061 20200514 MGI 1314838 Pcdh20 protocadherin 20 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1314838 Pcdh20 protocadherin 20 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1314842 Ipp IAP promoted placental gene gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1314842 Ipp IAP promoted placental gene gene MP:0001523 impaired righting response IEA N RGD:5509061 20181227 MGI 1314842 Ipp IAP promoted placental gene gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1314842 Ipp IAP promoted placental gene gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20220811 MGI 1314842 Ipp IAP promoted placental gene gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1314842 Ipp IAP promoted placental gene gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20211021 MGI 1314843 Eef1akmt2 EEF1A lysine methyltransferase 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201022 MGI 1314843 Eef1akmt2 EEF1A lysine methyltransferase 2 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1314843 Eef1akmt2 EEF1A lysine methyltransferase 2 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20201022 MGI 1314847 Adam21 a disintegrin and metallopeptidase domain 21 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:34631320 1314848 Tmem203 transmembrane protein 203 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1314848 Tmem203 transmembrane protein 203 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20181227 MGI 1314848 Tmem203 transmembrane protein 203 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20160602 MGI PMID:25996873 1314848 Tmem203 transmembrane protein 203 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20160602 MGI PMID:25996873 1314848 Tmem203 transmembrane protein 203 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160602 MGI PMID:25996873 1314848 Tmem203 transmembrane protein 203 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1314848 Tmem203 transmembrane protein 203 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1314848 Tmem203 transmembrane protein 203 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20160602 MGI PMID:25996873 1314848 Tmem203 transmembrane protein 203 gene MP:0001925 male infertility IAGP N RGD:5509061 20160602 MGI PMID:25996873 1314848 Tmem203 transmembrane protein 203 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 1314848 Tmem203 transmembrane protein 203 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1314848 Tmem203 transmembrane protein 203 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20160602 MGI PMID:25996873 1314848 Tmem203 transmembrane protein 203 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20160602 MGI PMID:25996873 1314848 Tmem203 transmembrane protein 203 gene MP:0005159 azoospermia IAGP N RGD:5509061 20160602 MGI PMID:25996873 1314848 Tmem203 transmembrane protein 203 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1314848 Tmem203 transmembrane protein 203 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210128 MGI 1314848 Tmem203 transmembrane protein 203 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1314848 Tmem203 transmembrane protein 203 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20160602 MGI PMID:25996873 1314848 Tmem203 transmembrane protein 203 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1314848 Tmem203 transmembrane protein 203 gene MP:0020352 abnormal endoplasmic reticulum physiology IAGP N RGD:5509061 20161013 MGI PMID:25996873 1314850 Tjp1 tight junction protein 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0000601 small liver IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23977053 1314850 Tjp1 tight junction protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0003891 increased allantois apoptosis IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0004557 dilated allantois IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0004969 pale kidney IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0008991 abnormal bile canaliculus morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0009501 abnormal hepatic duct morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0011402 renal cast IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0011534 granular kidney IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0011855 abnormal glomerular filtration barrier morphology IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0011869 detached podocyte IAGP N RGD:5509061 20160602 MGI PMID:25184792 1314850 Tjp1 tight junction protein 1 gene MP:0012246 abnormal hepatic cord morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 1314850 Tjp1 tight junction protein 1 gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314850 Tjp1 tight junction protein 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20151203 MGI PMID:18353970 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20191010 MGI PMID:12787314 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20191010 MGI PMID:12787314 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20191010 MGI PMID:12787314 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20191010 MGI PMID:12787314 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20191010 MGI PMID:12787314 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000745 tremors IEA N RGD:5509061 20111116 MGI 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:1061118 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:2726749 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:1061118 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:11884758 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20191010 MGI PMID:12787313 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:16465590 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20191010 MGI PMID:12787313 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20191010 MGI PMID:12787313 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:3678603 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:7891151 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:1061118 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11884758 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16465590 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:2726749 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:2077109 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:3678603 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20191010 MGI PMID:12787313 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:1061118 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11884758 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20191010 MGI PMID:12787313 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21824473 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001017 abnormal stellate ganglion morphology IAGP N RGD:5509061 20191010 MGI PMID:12787313 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20191010 MGI PMID:12787313 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20181011 MGI PMID:27831556 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:16465590 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:1061118 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11884758 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16465590 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:2726749 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20191010 MGI PMID:12787313 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20191010 MGI PMID:12787314 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20181011 MGI PMID:27831556 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20191010 MGI PMID:12787313 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:11884758 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001921 reduced fertility IEA N RGD:5509061 20111116 MGI 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11884758 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:1061118 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001924 infertility IEA N RGD:5509061 20111116 MGI 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:1061118 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11884758 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16465590 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:2726749 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20191010 MGI PMID:12787313 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20191010 MGI PMID:12787313 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:2726749 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20191010 MGI PMID:12787314 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20191010 MGI PMID:12787313 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20191010 MGI PMID:12787314 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:1061118 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11884758 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:1061118 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11884758 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20191010 MGI PMID:12787313 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0003205 testicular atrophy IEA N RGD:5509061 20111116 MGI 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0003727 abnormal retina layer morphology IEA N RGD:5509061 20111116 MGI 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16465590 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16465590 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16465590 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21824473 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21824473 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20191010 MGI PMID:12787314 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0003993 abnormal ventral spinal root morphology IEA N RGD:5509061 20111116 MGI 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21824473 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21824473 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20111116 MGI 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20191010 MGI PMID:12787314 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20191010 MGI PMID:12787314 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:2726749 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21824473 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0005578 teratozoospermia IEA N RGD:5509061 20111116 MGI 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20191010 MGI PMID:12787313 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1061118 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11884758 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20191010 MGI PMID:12787314 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20191010 MGI PMID:12787314 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:21824473 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0008282 enlarged hippocampus IEA N RGD:5509061 20111116 MGI 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:1061118 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:11884758 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21824473 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:2726749 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200123 MGI PMID:28104815 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:16465590 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21824473 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:7891151 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0009280 decreased activated sperm motility IEA N RGD:5509061 20111116 MGI 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0009400 decreased skeletal muscle fiber size IEA N RGD:5509061 20111116 MGI 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0009434 paraparesis IEA N RGD:5509061 20111116 MGI 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0009954 abnormal mitral cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11884758 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0012490 abnormal cochlear VIII nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:2077109 1314854 Agtpbp1 ATP/GTP binding protein 1 gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20200123 MGI PMID:28104815 1314856 Mettl16 methyltransferase 16, N6-methyladenosine gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1314856 Mettl16 methyltransferase 16, N6-methyladenosine gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1314856 Mettl16 methyltransferase 16, N6-methyladenosine gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160421 MGI 1314856 Mettl16 methyltransferase 16, N6-methyladenosine gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 1314856 Mettl16 methyltransferase 16, N6-methyladenosine gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1314856 Mettl16 methyltransferase 16, N6-methyladenosine gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1314856 Mettl16 methyltransferase 16, N6-methyladenosine gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20181004 MGI PMID:30197299 1314856 Mettl16 methyltransferase 16, N6-methyladenosine gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314856 Mettl16 methyltransferase 16, N6-methyladenosine gene MP:0011471 decreased urine creatinine level IEA N RGD:5509061 20211021 MGI 1314856 Mettl16 methyltransferase 16, N6-methyladenosine gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1314856 Mettl16 methyltransferase 16, N6-methyladenosine gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1314858 Mbip MAP3K12 binding inhibitory protein 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1314858 Mbip MAP3K12 binding inhibitory protein 1 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20240919 MGI 1314858 Mbip MAP3K12 binding inhibitory protein 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1314858 Mbip MAP3K12 binding inhibitory protein 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1314858 Mbip MAP3K12 binding inhibitory protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1314858 Mbip MAP3K12 binding inhibitory protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 1314860 Lamb1 laminin B1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180118 MGI PMID:26705335 1314860 Lamb1 laminin B1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20180118 MGI PMID:26705335 1314860 Lamb1 laminin B1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20180118 MGI PMID:26705335 1314860 Lamb1 laminin B1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20180118 MGI PMID:26705335 1314860 Lamb1 laminin B1 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:15102706 1314860 Lamb1 laminin B1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20180118 MGI PMID:26705335 1314860 Lamb1 laminin B1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15102706 1314860 Lamb1 laminin B1 gene MP:0002980 abnormal postural reflex IAGP N RGD:5509061 20180118 MGI PMID:26705335 1314860 Lamb1 laminin B1 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20180118 MGI PMID:26705335 1314860 Lamb1 laminin B1 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20180118 MGI PMID:26705335 1314860 Lamb1 laminin B1 gene MP:0005323 dystonia IAGP N RGD:5509061 20180118 MGI PMID:26705335 1314860 Lamb1 laminin B1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15102706 1314860 Lamb1 laminin B1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1314860 Lamb1 laminin B1 gene MP:0011187 abnormal parietal endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15102706 1314860 Lamb1 laminin B1 gene MP:0012057 abnormal mural trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15102706 1314860 Lamb1 laminin B1 gene MP:0013179 wavy tail IAGP N RGD:5509061 20180118 MGI PMID:26705335 1314862 Wnt8a wingless-type MMTV integration site family, member 8A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23041177 1314862 Wnt8a wingless-type MMTV integration site family, member 8A gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:23041177 1314866 Rpl3l ribosomal protein L3-like gene MP:0002188 small heart IAGP N RGD:5509061 20230302 MGI PMID:36733907 1314866 Rpl3l ribosomal protein L3-like gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20230302 MGI PMID:36733907 1314866 Rpl3l ribosomal protein L3-like gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20230601 MGI PMID:37080962 1314866 Rpl3l ribosomal protein L3-like gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20230601 MGI PMID:37080962 1314870 Sec61g SEC61 translocon subunit gamma gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241017 MGI 1314870 Sec61g SEC61 translocon subunit gamma gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1314870 Sec61g SEC61 translocon subunit gamma gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241017 MGI 1314872 Rpl12 ribosomal protein L12 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1314872 Rpl12 ribosomal protein L12 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1314872 Rpl12 ribosomal protein L12 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1314872 Rpl12 ribosomal protein L12 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1314872 Rpl12 ribosomal protein L12 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1314872 Rpl12 ribosomal protein L12 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20210128 MGI 1314872 Rpl12 ribosomal protein L12 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1314872 Rpl12 ribosomal protein L12 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1314872 Rpl12 ribosomal protein L12 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1314872 Rpl12 ribosomal protein L12 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1314872 Rpl12 ribosomal protein L12 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1314872 Rpl12 ribosomal protein L12 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1314872 Rpl12 ribosomal protein L12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314872 Rpl12 ribosomal protein L12 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1314876 Tfap2b transcription factor AP-2 beta gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0000532 kidney vascular congestion IAGP N RGD:5509061 20200402 MGI PMID:29804851 1314876 Tfap2b transcription factor AP-2 beta gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200402 MGI PMID:29804851 1314876 Tfap2b transcription factor AP-2 beta gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0002183 gliosis IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20200402 MGI PMID:29804851 1314876 Tfap2b transcription factor AP-2 beta gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:9271117 1314876 Tfap2b transcription factor AP-2 beta gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:21829553 1314876 Tfap2b transcription factor AP-2 beta gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20200402 MGI PMID:29804851 1314876 Tfap2b transcription factor AP-2 beta gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:9271117 1314876 Tfap2b transcription factor AP-2 beta gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200402 MGI PMID:29804851 1314876 Tfap2b transcription factor AP-2 beta gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9271117 1314876 Tfap2b transcription factor AP-2 beta gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0004222 iris synechia IEA N RGD:5509061 20220811 MGI 1314876 Tfap2b transcription factor AP-2 beta gene MP:0004283 absent cornea endothelium IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0005497 optic nerve cupping IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20200402 MGI PMID:29804851 1314876 Tfap2b transcription factor AP-2 beta gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:21829553 1314876 Tfap2b transcription factor AP-2 beta gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0008259 abnormal optic disk morphology IAGP N RGD:5509061 20190411 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0009744 postaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:21829553 1314876 Tfap2b transcription factor AP-2 beta gene MP:0009859 eye opacity IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:21829553 1314876 Tfap2b transcription factor AP-2 beta gene MP:0010052 increased grip strength IEA N RGD:5509061 20181227 MGI 1314876 Tfap2b transcription factor AP-2 beta gene MP:0010252 anterior subcapsular cataract IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0010564 abnormal fetal ductus arteriosus morphology IAGP N RGD:5509061 20200402 MGI PMID:29804851 1314876 Tfap2b transcription factor AP-2 beta gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20141003 MGI PMID:21829553 1314876 Tfap2b transcription factor AP-2 beta gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12695560 1314876 Tfap2b transcription factor AP-2 beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9271117 1314876 Tfap2b transcription factor AP-2 beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200402 MGI PMID:29804851 1314876 Tfap2b transcription factor AP-2 beta gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21829553 1314876 Tfap2b transcription factor AP-2 beta gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240516 MGI PMID:32878901 1314876 Tfap2b transcription factor AP-2 beta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314876 Tfap2b transcription factor AP-2 beta gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9271117 1314876 Tfap2b transcription factor AP-2 beta gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20180503 MGI PMID:27483349 1314876 Tfap2b transcription factor AP-2 beta gene MP:0012287 increased frequency of paradoxical sleep IAGP N RGD:5509061 20240516 MGI PMID:32878901 1314876 Tfap2b transcription factor AP-2 beta gene MP:0012289 abnormal non-rapid eye movement sleep pattern IAGP N RGD:5509061 20240516 MGI PMID:32878901 1314876 Tfap2b transcription factor AP-2 beta gene MP:0020478 abnormal circadian sleep/wake cycle IAGP N RGD:5509061 20240516 MGI PMID:32878901 1314876 Tfap2b transcription factor AP-2 beta gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:27483349 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:18776146 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:18776146 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:18776146 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:18776146 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20220428 MGI PMID:31060802 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:18776146 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20220428 MGI PMID:31060802 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20220428 MGI PMID:31060802 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:18776146 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20220428 MGI PMID:31060802 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20220428 MGI PMID:31060802 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0003586 dilated ureter IAGP N RGD:5509061 20141003 MGI PMID:18776146 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20220428 MGI PMID:31060802 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:18776146 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20141003 MGI PMID:18776146 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20220428 MGI PMID:31060802 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20220428 MGI PMID:31060802 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:18776146 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18776146 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0011426 abnormal ureter smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:18776146 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0011480 impaired ureteric peristalsis IAGP N RGD:5509061 20141003 MGI PMID:18776146 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20220428 MGI PMID:31060802 1314878 Tshz3 teashirt zinc finger family member 3 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20220428 MGI PMID:31060802 1314885 Tada3 transcriptional adaptor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22736770 1314885 Tada3 transcriptional adaptor 3 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:22736770 1314885 Tada3 transcriptional adaptor 3 gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:22736770 1314885 Tada3 transcriptional adaptor 3 gene MP:0010039 abnormal trophoblast giant cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22736770 1314885 Tada3 transcriptional adaptor 3 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22736770 1314885 Tada3 transcriptional adaptor 3 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22736770 1314885 Tada3 transcriptional adaptor 3 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22736770 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17332334 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16170338 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17332334 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16170338 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17332334 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:16170338 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:16170338 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16170338 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17332334 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16170338 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16170338 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17332334 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17332334 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:17693408 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:16170338 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17332334 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:17332334 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:17693408 1314891 Ing1 inhibitor of growth family, member 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17332334 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0000751 myopathy IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0021206 abnormal limb muscle morphology IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314893 Asnsd1 asparagine synthetase domain containing 1 gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20240418 MGI PMID:32638637 1314898 Arid3b AT-rich interaction domain 3B gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16530748 1314898 Arid3b AT-rich interaction domain 3B gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:16530748 1314898 Arid3b AT-rich interaction domain 3B gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:16530748 1314898 Arid3b AT-rich interaction domain 3B gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:16530748 1314898 Arid3b AT-rich interaction domain 3B gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:27537840 1314898 Arid3b AT-rich interaction domain 3B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21199920 1314898 Arid3b AT-rich interaction domain 3B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16530748 1314898 Arid3b AT-rich interaction domain 3B gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:16530748 1314898 Arid3b AT-rich interaction domain 3B gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170209 MGI PMID:27537840 1314898 Arid3b AT-rich interaction domain 3B gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16530748 1314898 Arid3b AT-rich interaction domain 3B gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:16530748 1314898 Arid3b AT-rich interaction domain 3B gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20170209 MGI PMID:27537840 1314898 Arid3b AT-rich interaction domain 3B gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20170209 MGI PMID:27537840 1314898 Arid3b AT-rich interaction domain 3B gene MP:0008170 decreased B-1b cell number IAGP N RGD:5509061 20170209 MGI PMID:27537840 1314898 Arid3b AT-rich interaction domain 3B gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20170209 MGI PMID:27537840 1314898 Arid3b AT-rich interaction domain 3B gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20170209 MGI PMID:27537840 1314898 Arid3b AT-rich interaction domain 3B gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20170209 MGI PMID:27537840 1314898 Arid3b AT-rich interaction domain 3B gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20170209 MGI PMID:27537840 1314898 Arid3b AT-rich interaction domain 3B gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20170209 MGI PMID:27537840 1314898 Arid3b AT-rich interaction domain 3B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21199920 1314898 Arid3b AT-rich interaction domain 3B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16530748 1314898 Arid3b AT-rich interaction domain 3B gene MP:0011816 decreased pre-pro B cell number IAGP N RGD:5509061 20170209 MGI PMID:27537840 1314898 Arid3b AT-rich interaction domain 3B gene MP:0013893 decreased common lymphocyte progenitor cell number IAGP N RGD:5509061 20170209 MGI PMID:27537840 1314900 Acp6 acid phosphatase 6, lysophosphatidic gene MP:0000745 tremors IEA N RGD:5509061 20230119 MGI 1314900 Acp6 acid phosphatase 6, lysophosphatidic gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1314900 Acp6 acid phosphatase 6, lysophosphatidic gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20230119 MGI 1314900 Acp6 acid phosphatase 6, lysophosphatidic gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230119 MGI 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0003794 delayed somite formation IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0004573 absent limb buds IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0004785 abnormal posterior cardinal vein morphology IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0006294 absent optic vesicle IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0010951 abnormal lipid oxidation IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0012177 delayed head development IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0012552 lactic acidosis IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0012708 delayed rostral neuropore closure IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0013906 absent embryonic telencephalon IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0014012 abnormal cranial blood vasculature morphology IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314902 Hacd2 3-hydroxyacyl-CoA dehydratase 2 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20230406 MGI PMID:36693621 1314905 Zfp110 zinc finger protein 110 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10545116 1314905 Zfp110 zinc finger protein 110 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10545116 1314905 Zfp110 zinc finger protein 110 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10545116 1314905 Zfp110 zinc finger protein 110 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10545116 1314905 Zfp110 zinc finger protein 110 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10545116 1314905 Zfp110 zinc finger protein 110 gene MP:0030006 decreased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:10545116 1314906 Diaph3 diaphanous related formin 3 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20201002 MGI PMID:26471482 1314906 Diaph3 diaphanous related formin 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24239357 1314906 Diaph3 diaphanous related formin 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20201002 MGI PMID:26471482 1314906 Diaph3 diaphanous related formin 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20201002 MGI PMID:26471482 1314906 Diaph3 diaphanous related formin 3 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20160811 MGI 1314906 Diaph3 diaphanous related formin 3 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20160811 MGI 1314906 Diaph3 diaphanous related formin 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20201002 MGI PMID:26471482 1314906 Diaph3 diaphanous related formin 3 gene MP:0001577 anemia IAGP N RGD:5509061 20201002 MGI PMID:26471482 1314906 Diaph3 diaphanous related formin 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1314906 Diaph3 diaphanous related formin 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:24239357 1314906 Diaph3 diaphanous related formin 3 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20160811 MGI 1314906 Diaph3 diaphanous related formin 3 gene MP:0002546 mydriasis IEA N RGD:5509061 20210520 MGI 1314906 Diaph3 diaphanous related formin 3 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20160421 MGI 1314906 Diaph3 diaphanous related formin 3 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20201002 MGI PMID:26471482 1314906 Diaph3 diaphanous related formin 3 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20220519 MGI 1314906 Diaph3 diaphanous related formin 3 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20220519 MGI 1314906 Diaph3 diaphanous related formin 3 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20201002 MGI PMID:26471482 1314906 Diaph3 diaphanous related formin 3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20201002 MGI PMID:26471482 1314906 Diaph3 diaphanous related formin 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:24239357 1314906 Diaph3 diaphanous related formin 3 gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1314906 Diaph3 diaphanous related formin 3 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1314906 Diaph3 diaphanous related formin 3 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20201002 MGI PMID:26471482 1314906 Diaph3 diaphanous related formin 3 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160421 MGI 1314906 Diaph3 diaphanous related formin 3 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20201002 MGI PMID:26471482 1314906 Diaph3 diaphanous related formin 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24239357 1314906 Diaph3 diaphanous related formin 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20201001 MGI PMID:26471482 1314906 Diaph3 diaphanous related formin 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314906 Diaph3 diaphanous related formin 3 gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:24239357 1314906 Diaph3 diaphanous related formin 3 gene MP:0012397 abnormal nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24239357 1314910 Tvp23b trans-golgi network vesicle protein 23B gene MP:0005036 diarrhea IAGP N RGD:5509061 20231102 MGI PMID:37339972 1314910 Tvp23b trans-golgi network vesicle protein 23B gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20231102 MGI PMID:37339972 1314910 Tvp23b trans-golgi network vesicle protein 23B gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1314910 Tvp23b trans-golgi network vesicle protein 23B gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20231102 MGI PMID:37339972 1314910 Tvp23b trans-golgi network vesicle protein 23B gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20231102 MGI PMID:37339972 1314910 Tvp23b trans-golgi network vesicle protein 23B gene MP:0013799 abnormal intestinal goblet cell physiology IAGP N RGD:5509061 20231102 MGI PMID:37339972 1314910 Tvp23b trans-golgi network vesicle protein 23B gene MP:0014222 decreased colon goblet cell number IAGP N RGD:5509061 20231102 MGI PMID:37339972 1314911 Znfx1 zinc finger, NFX1-type containing 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1314911 Znfx1 zinc finger, NFX1-type containing 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1314914 Ubxn7 UBX domain protein 7 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20190502 MGI 1314914 Ubxn7 UBX domain protein 7 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1314914 Ubxn7 UBX domain protein 7 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1314914 Ubxn7 UBX domain protein 7 gene MP:0009931 abnormal skin appearance IEA N RGD:5509061 20190502 MGI 1314914 Ubxn7 UBX domain protein 7 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1314914 Ubxn7 UBX domain protein 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314914 Ubxn7 UBX domain protein 7 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0000480 increased rib number IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0001265 decreased body size IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20170105 MGI 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0001926 female infertility IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0002637 small uterus IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0002673 abnormal sperm number IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0002833 increased heart weight IEA N RGD:5509061 20181227 MGI 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0005251 blepharitis IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0006236 absent Meibomian glands IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20170105 MGI 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0008258 thin endometrium IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0009096 decreased endometrial gland number IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0009669 abnormal postimplantation uterine environment IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0010855 pulmonary hyperemia IAGP N RGD:5509061 20141003 MGI PMID:24012418 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0013192 decreased sebaceous gland number IAGP N RGD:5509061 20160317 MGI PMID:26333994 1314919 Ash1l ASH1 like histone lysine methyltransferase gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1314920 Tmtc3 transmembrane and tetratricopeptide repeat containing 3 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:21956870 1314920 Tmtc3 transmembrane and tetratricopeptide repeat containing 3 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:21956870 1314920 Tmtc3 transmembrane and tetratricopeptide repeat containing 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:21956870 1314920 Tmtc3 transmembrane and tetratricopeptide repeat containing 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21956870 1314920 Tmtc3 transmembrane and tetratricopeptide repeat containing 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:21956870 1314920 Tmtc3 transmembrane and tetratricopeptide repeat containing 3 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20211021 MGI 1314920 Tmtc3 transmembrane and tetratricopeptide repeat containing 3 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20211021 MGI 1314920 Tmtc3 transmembrane and tetratricopeptide repeat containing 3 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21956870 1314920 Tmtc3 transmembrane and tetratricopeptide repeat containing 3 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:21956870 1314920 Tmtc3 transmembrane and tetratricopeptide repeat containing 3 gene MP:0010906 abnormal lung bud morphology IAGP N RGD:5509061 20141003 MGI PMID:21956870 1314920 Tmtc3 transmembrane and tetratricopeptide repeat containing 3 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:21956870 1314920 Tmtc3 transmembrane and tetratricopeptide repeat containing 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21956870 1314920 Tmtc3 transmembrane and tetratricopeptide repeat containing 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1314922 Fbxo3 F-box protein 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1314925 Svil supervillin gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:22550155 1314925 Svil supervillin gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:22550155 1314925 Svil supervillin gene MP:0009586 increased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:22550155 1314925 Svil supervillin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230119 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20160922 MGI PMID:24652767 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20160922 MGI PMID:24652767 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20141003 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20160804 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20160804 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0001258 decreased body length IAGP N RGD:5509061 20160922 MGI PMID:24652767 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160922 MGI PMID:24652767 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20141003 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20141003 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20141003 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20141003 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20141003 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20141003 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20141003 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20160922 MGI PMID:24652767 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20160922 MGI PMID:24652767 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20160922 MGI PMID:24652767 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20160922 MGI PMID:24652767 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0005316 abnormal response to tactile stimuli IEA N RGD:5509061 20141003 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20141003 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20160804 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20160804 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0008805 decreased circulating amylase level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20160922 MGI PMID:24652767 1314927 Slc38a10 solute carrier family 38, member 10 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20160922 MGI PMID:24652767 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20231207 MGI 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0001148 enlarged testis IEA N RGD:5509061 20210826 MGI 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20190926 MGI PMID:28945193 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20190926 MGI PMID:28945193 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20221215 MGI 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210826 MGI 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20211021 MGI 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20190926 MGI PMID:28945193 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20190926 MGI PMID:28945193 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20190926 MGI PMID:28945193 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20190926 MGI PMID:28945193 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20190926 MGI PMID:28945193 1314929 Sun5 Sad1 and UNC84 domain containing 5 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20190926 MGI PMID:28945193 1314933 Chfr checkpoint with forkhead and ring finger domains gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15793587 1314933 Chfr checkpoint with forkhead and ring finger domains gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15793587 1314933 Chfr checkpoint with forkhead and ring finger domains gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:15793587 1314933 Chfr checkpoint with forkhead and ring finger domains gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:15793587 1314933 Chfr checkpoint with forkhead and ring finger domains gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15793587 1314933 Chfr checkpoint with forkhead and ring finger domains gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15793587 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11756548 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001260 increased body weight IAGP N RGD:5509061 20141030 MGI PMID:24385930 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001399 hyperactivity IEA N RGD:5509061 20200514 MGI 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15921919 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141030 MGI PMID:24385930 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160204 MGI PMID:25866966 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11895368 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141030 MGI PMID:24385930 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160204 MGI PMID:25866966 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20160204 MGI PMID:25866966 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11895368 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20160204 MGI PMID:25866966 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:15921919 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:15921919 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22916201 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11756548 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11756548 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11756548 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20201022 MGI 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:15921919 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:15921919 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:11895368 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141030 MGI PMID:24385930 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20160204 MGI PMID:25866966 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15590147 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141030 MGI PMID:24385930 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20160204 MGI PMID:25866966 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20230907 MGI PMID:37389991 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002608 increased hematocrit IEA N RGD:5509061 20211021 MGI 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11756548 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20200514 MGI 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20170413 MGI PMID:26869263 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20230907 MGI PMID:37389991 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:17940072 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20160204 MGI PMID:25866966 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0003356 impaired luteinization IAGP N RGD:5509061 20141003 MGI PMID:11756548 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20160204 MGI PMID:25866966 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20141003 MGI PMID:11756548 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0003962 abnormal adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:22916201 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20170413 MGI PMID:26869263 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11756548 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:11756548 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:11756548 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0004962 decreased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:11756548 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:15921919 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:11756548 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:11756548 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:17940072 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:11895368 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:15590147 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:15921919 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11895368 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141030 MGI PMID:24385930 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:22916201 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20210128 MGI 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9808466 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0011940 decreased food intake IEA N RGD:5509061 20200514 MGI 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0020870 decreased thigmotaxis IAGP N RGD:5509061 20230907 MGI PMID:37389991 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20230907 MGI PMID:37389991 1314935 Ube3a ubiquitin protein ligase E3A gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20230907 MGI PMID:37389991 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0001314 cornea opacity IEA N RGD:5509061 20231207 MGI 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20231207 MGI 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0002649 abnormal enamel rod pattern IAGP N RGD:5509061 20141003 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0002764 short tibia IEA N RGD:5509061 20160114 MGI 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0003404 absent enamel IAGP N RGD:5509061 20141003 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0006133 calcified artery IAGP N RGD:5509061 20141003 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0006402 small molars IAGP N RGD:5509061 20141003 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20231207 MGI 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0010923 calcified pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0011309 abnormal kidney arterial blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0030138 abnormal lower incisor color IAGP N RGD:5509061 20171005 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0030139 abnormal upper incisor color IAGP N RGD:5509061 20171005 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20171228 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0030458 abnormal tooth wear IAGP N RGD:5509061 20171228 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0030460 enamel pits IAGP N RGD:5509061 20171221 MGI PMID:22732358 1314940 Fam20a FAM20A, golgi associated secretory pathway pseudokinase gene MP:0030500 conical molar IAGP N RGD:5509061 20171228 MGI PMID:22732358 1314944 Gtpbp2 GTP binding protein 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20160811 MGI 1314944 Gtpbp2 GTP binding protein 2 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1314944 Gtpbp2 GTP binding protein 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20141003 MGI 1314944 Gtpbp2 GTP binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20210826 MGI 1314944 Gtpbp2 GTP binding protein 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0008103 amacrine cell degeneration IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0008265 abnormal hippocampus CA2 region morphology IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20190815 MGI PMID:25061210 1314944 Gtpbp2 GTP binding protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20160421 MGI 1314944 Gtpbp2 GTP binding protein 2 gene MP:0021081 abnormal ribosomal stalling IAGP N RGD:5509061 20220310 MGI PMID:25061210 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19139201 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19139201 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:17565376 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:17565376 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15692052 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17565376 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:15692051 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:19139201 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15692051 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210826 MGI 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:17565376 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18261938 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:15692052 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:14560001 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15692051 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18261938 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:19898471 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:19139201 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16407890 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:19218085 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17565376 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:19139201 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17565376 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:19139201 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17565376 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008132 increased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:17565376 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008136 enlarged Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:17565376 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:19898471 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:15692052 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:17565376 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19139201 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18261938 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:19139201 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008599 increased circulating interleukin-2 level IAGP N RGD:5509061 20141003 MGI PMID:19139201 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:15692052 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:18261938 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:15692052 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:17565376 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:14560001 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:15692051 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:17565376 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:17565376 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17565376 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15692052 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19139201 1314946 Nod2 nucleotide-binding oligomerization domain containing 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20240627 MGI 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20181108 MGI PMID:26755066 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20220428 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0004043 abnormal pH regulation IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0011000 abnormal allogrooming behavior IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0011617 abnormal habituation IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20181108 MGI PMID:26755066 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20181108 MGI PMID:26755066 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0020396 abnormal social recognition IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0020437 abnormal social play behavior IAGP N RGD:5509061 20181025 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0020852 abnormal olfactory behavior IAGP N RGD:5509061 20181101 MGI PMID:29362376 1314948 Slc9a9 solute carrier family 9 (sodium/hydrogen exchanger), member 9 gene MP:0030950 abnormal synaptic vesicle exocytosis IAGP N RGD:5509061 20190725 MGI PMID:29362376 1314954 Mgst3 microsomal glutathione S-transferase 3 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1314954 Mgst3 microsomal glutathione S-transferase 3 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0000243 myoclonus IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20150827 MGI PMID:24859200 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0000917 obstructive hydrocephaly IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0002064 seizures IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20181227 MGI 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20150827 MGI PMID:24859200 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20150827 MGI PMID:24859200 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20150827 MGI PMID:24859200 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20181227 MGI 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20181227 MGI 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20150827 MGI PMID:24859200 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20150827 MGI PMID:24859200 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20150827 MGI PMID:24859200 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0011724 ectopic cortical neuron IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0012474 decreased cingulate cortex size IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0012506 brain atrophy IAGP N RGD:5509061 20150618 MGI PMID:18562329 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0013908 small lateral ventricles IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0020762 abnormal dorsal subiculum morphology IAGP N RGD:5509061 20201210 MGI PMID:31173351 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20210429 MGI PMID:32221352 1314955 Eml1 echinoderm microtubule associated protein like 1 gene MP:0030245 round head IEA N RGD:5509061 20190418 MGI 1314959 Alkbh2 alkB homolog 2, alpha-ketoglutarate-dependent dioxygenase gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:16642038 1314961 Kdm4a lysine (K)-specific demethylase 4A gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21555854 1314961 Kdm4a lysine (K)-specific demethylase 4A gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21555854 1314961 Kdm4a lysine (K)-specific demethylase 4A gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:21555854 1314961 Kdm4a lysine (K)-specific demethylase 4A gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:21555854 1314961 Kdm4a lysine (K)-specific demethylase 4A gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21555854 1314964 Gulp1 GULP, engulfment adaptor PTB domain containing 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1314964 Gulp1 GULP, engulfment adaptor PTB domain containing 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1314967 Taf1b TATA-box binding protein associated factor, RNA polymerase I, B gene MP:0008830 abnormal nucleolus morphology IAGP N RGD:5509061 20220324 MGI PMID:35139074 1314967 Taf1b TATA-box binding protein associated factor, RNA polymerase I, B gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20220324 MGI PMID:35139074 1314967 Taf1b TATA-box binding protein associated factor, RNA polymerase I, B gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20220324 MGI PMID:35139074 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201231 MGI 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:12055593 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:9009202 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0001805 decreased IgG level IEA N RGD:5509061 20180215 MGI 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12055593 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:12055593 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0002392 abnormal Peyer's patch T cell area morphology IAGP N RGD:5509061 20141003 MGI PMID:12055593 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16148099 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9009202 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:16148099 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16148099 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24244019 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0002491 decreased IgD level IEA N RGD:5509061 20181004 MGI 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0002492 decreased IgE level IEA N RGD:5509061 20180215 MGI 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0002494 increased IgM level IEA N RGD:5509061 20181004 MGI 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16148099 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20181227 MGI 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210128 MGI 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20180215 MGI 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12055593 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24244019 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24244019 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0005425 increased macrophage cell number IEA N RGD:5509061 20180215 MGI 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16148099 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0006173 abnormal myeloid dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12055593 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181004 MGI 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008125 abnormal dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:12055593 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:12055593 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12055593 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008170 decreased B-1b cell number IEA N RGD:5509061 20180215 MGI 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:24244019 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:24244019 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008196 abnormal follicular dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12055593 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008240 abnormal spleen marginal zone macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008241 abnormal metallophilic macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:9009202 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008524 increased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:12055593 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9133427 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:24244019 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:24244019 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20181004 MGI 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0010848 decreased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20190606 MGI 1314972 Bcl3 B cell leukemia/lymphoma 3 gene MP:0014350 disorganized spleen B cell follicle IAGP N RGD:5509061 20240104 MGI PMID:9133427 1314974 Mrpl18 mitochondrial ribosomal protein L18 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 1314974 Mrpl18 mitochondrial ribosomal protein L18 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1314974 Mrpl18 mitochondrial ribosomal protein L18 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314974 Mrpl18 mitochondrial ribosomal protein L18 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1314976 Klhl2 kelch-like 2, Mayven gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20191010 MGI PMID:28414128 1314976 Klhl2 kelch-like 2, Mayven gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1314978 Foxn4 forkhead box N4 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15363391 1314978 Foxn4 forkhead box N4 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15363391 1314978 Foxn4 forkhead box N4 gene MP:0006070 increased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:15363391 1314978 Foxn4 forkhead box N4 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15363391 1314978 Foxn4 forkhead box N4 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:15363391 1314978 Foxn4 forkhead box N4 gene MP:0008107 absent retina horizontal cells IAGP N RGD:5509061 20141003 MGI PMID:15363391 1314978 Foxn4 forkhead box N4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15363391 1314978 Foxn4 forkhead box N4 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:15363391 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20200924 MGI PMID:32341096 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0001505 hunched posture IAGP N RGD:5509061 20200723 MGI PMID:21217823 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20200723 MGI PMID:21217823 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0002083 premature death IAGP N RGD:5509061 20200723 MGI PMID:21217823 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200723 MGI PMID:21217823 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200924 MGI PMID:32341096 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20200723 MGI PMID:21217823 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191205 MGI 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0003087 absent allantois IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200723 MGI PMID:21217823 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0005150 cachexia IAGP N RGD:5509061 20200723 MGI PMID:21217823 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0005202 lethargy IAGP N RGD:5509061 20200723 MGI PMID:21217823 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20230601 MGI 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20200723 MGI PMID:21217823 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0008912 nervous IAGP N RGD:5509061 20200723 MGI PMID:21217823 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200924 MGI PMID:32341096 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0012315 impaired learning IAGP N RGD:5509061 20200924 MGI PMID:32341096 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0012724 absent head fold IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191205 MGI 1314982 Mrpl3 mitochondrial ribosomal protein L3 gene MP:0014246 decreased cellular ATP level IAGP N RGD:5509061 20241024 MGI PMID:32376682 1314988 Tctn2 tectonic family member 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21565611 1314988 Tctn2 tectonic family member 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21565611 1314988 Tctn2 tectonic family member 2 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:21565611 1314988 Tctn2 tectonic family member 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21565611 1314988 Tctn2 tectonic family member 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:21565611 1314988 Tctn2 tectonic family member 2 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:21725307 1314988 Tctn2 tectonic family member 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21725307 1314988 Tctn2 tectonic family member 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:21725307 1314988 Tctn2 tectonic family member 2 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:21565611 1314988 Tctn2 tectonic family member 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:21565611 1314988 Tctn2 tectonic family member 2 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:21565611 1314988 Tctn2 tectonic family member 2 gene MP:0011261 abnormal limb mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:21725307 1314989 Cpsf4l cleavage and polyadenylation specific factor 4-like gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1314993 Ccnj cyclin J gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1314993 Ccnj cyclin J gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 1314993 Ccnj cyclin J gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1314996 Cnot8 CCR4-NOT transcription complex, subunit 8 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20210513 MGI PMID:31924127 1314996 Cnot8 CCR4-NOT transcription complex, subunit 8 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20210513 MGI PMID:31924127 1314997 Pus10 pseudouridylate synthase 10 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 1315003 Isg20 interferon-stimulated protein gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20240620 MGI PMID:37452495 1315003 Isg20 interferon-stimulated protein gene MP:0004041 increased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20240620 MGI PMID:37452495 1315003 Isg20 interferon-stimulated protein gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20240620 MGI PMID:37452495 1315003 Isg20 interferon-stimulated protein gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20240620 MGI PMID:37452495 1315005 Kcmf1 potassium channel modulatory factor 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:20473331 1315005 Kcmf1 potassium channel modulatory factor 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20473331 1315005 Kcmf1 potassium channel modulatory factor 1 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:20473331 1315005 Kcmf1 potassium channel modulatory factor 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:20473331 1315005 Kcmf1 potassium channel modulatory factor 1 gene MP:0009109 decreased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:20473331 1315005 Kcmf1 potassium channel modulatory factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20473331 1315005 Kcmf1 potassium channel modulatory factor 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20473331 1315009 Serf2 small EDRK-rich factor 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315011 Pop7 processing of precursor 7, ribonuclease P family, (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1315011 Pop7 processing of precursor 7, ribonuclease P family, (S. cerevisiae) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20190808 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190808 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23632887 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20190808 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20220519 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0005015 increased T cell number IEA N RGD:5509061 20201022 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20220811 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20210128 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0008126 increased dendritic cell number IEA N RGD:5509061 20220519 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20190808 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0013669 decreased Ly6C-positive immature NK cell number IEA N RGD:5509061 20201022 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0013670 increased Ly6C-positive immature NK cell number IEA N RGD:5509061 20201022 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0013676 increased Ly6C-positive mature NK cell number IEA N RGD:5509061 20201022 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0013679 increased Ly6C-positive NK T cell number IEA N RGD:5509061 20211021 MGI 1315013 Asb2 ankyrin repeat and SOCS box-containing 2 gene MP:0013771 decreased effector memory T-helper cell number IEA N RGD:5509061 20210128 MGI 1315017 Epn3 epsin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21115825 1315017 Epn3 epsin 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1315017 Epn3 epsin 3 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0000745 tremors IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0002083 premature death IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0004144 hypotonia IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0020070 decreased neocortex volume IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315023 Elp2 elongator acetyltransferase complex subunit 2 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20210909 MGI PMID:33976153 1315025 Klk7 kallikrein related-peptidase 7 (chymotryptic, stratum corneum) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180628 MGI PMID:29311134 1315025 Klk7 kallikrein related-peptidase 7 (chymotryptic, stratum corneum) gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20180628 MGI PMID:29311134 1315028 Cct7 chaperonin containing TCP1 subunit 7 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20240523 MGI 1315028 Cct7 chaperonin containing TCP1 subunit 7 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240926 MGI 1315028 Cct7 chaperonin containing TCP1 subunit 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1315028 Cct7 chaperonin containing TCP1 subunit 7 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1315028 Cct7 chaperonin containing TCP1 subunit 7 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240926 MGI 1315031 Snx17 sorting nexin 17 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20141003 MGI 1315031 Snx17 sorting nexin 17 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1315031 Snx17 sorting nexin 17 gene MP:0001293 anophthalmia IEA N RGD:5509061 20141003 MGI 1315031 Snx17 sorting nexin 17 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1315031 Snx17 sorting nexin 17 gene MP:0011661 persistent truncus arteriosus type i IEA N RGD:5509061 20141003 MGI 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20160825 MGI PMID:27225478 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0000774 decreased brain size IEA N RGD:5509061 20210520 MGI 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210520 MGI 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0002175 decreased brain weight IEA N RGD:5509061 20210826 MGI 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220519 MGI 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20160825 MGI PMID:27225478 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20160825 MGI PMID:27225478 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20231207 MGI 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20160825 MGI PMID:27225478 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0010580 decreased heart left ventricle size IAGP N RGD:5509061 20160825 MGI PMID:27225478 1315033 Dusp8 dual specificity phosphatase 8 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20160825 MGI PMID:27225478 1315035 Car9 carbonic anhydrase 9 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:16217040 1315035 Car9 carbonic anhydrase 9 gene MP:0002580 duodenal lesions IAGP N RGD:5509061 20141003 MGI PMID:12454846 1315035 Car9 carbonic anhydrase 9 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:16217040 1315035 Car9 carbonic anhydrase 9 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12454846 1315035 Car9 carbonic anhydrase 9 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:16217040 1315035 Car9 carbonic anhydrase 9 gene MP:0005493 stomach epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12454846 1315035 Car9 carbonic anhydrase 9 gene MP:0005493 stomach epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16217040 1315035 Car9 carbonic anhydrase 9 gene MP:0008210 increased mature B cell number IEA N RGD:5509061 20170323 MGI 1315035 Car9 carbonic anhydrase 9 gene MP:0010787 gastric cyst IAGP N RGD:5509061 20141003 MGI PMID:16217040 1315035 Car9 carbonic anhydrase 9 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:12454846 1315035 Car9 carbonic anhydrase 9 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16217040 1315035 Car9 carbonic anhydrase 9 gene MP:0013567 gastric gland atrophy IAGP N RGD:5509061 20150312 MGI PMID:16217040 1315041 Nmb neuromedin B gene MP:0001440 abnormal grooming behavior IAGP N RGD:5509061 20180201 MGI PMID:29133874 1315044 Map3k5 mitogen-activated protein kinase kinase kinase 5 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:14665690 1315044 Map3k5 mitogen-activated protein kinase kinase kinase 5 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:14665690 1315044 Map3k5 mitogen-activated protein kinase kinase kinase 5 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19214184 1315044 Map3k5 mitogen-activated protein kinase kinase kinase 5 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:11266364 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0000215 absent erythrocytes IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210520 MGI 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20595512 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20141003 MGI PMID:17826737 1315048 Rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1315051 Rabl3 RAB, member RAS oncogene family-like 3 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20200730 MGI PMID:32220963 1315051 Rabl3 RAB, member RAS oncogene family-like 3 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20200730 MGI PMID:32220963 1315051 Rabl3 RAB, member RAS oncogene family-like 3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20200730 MGI PMID:32220963 1315051 Rabl3 RAB, member RAS oncogene family-like 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200730 MGI PMID:32220963 1315051 Rabl3 RAB, member RAS oncogene family-like 3 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20200730 MGI PMID:32220963 1315051 Rabl3 RAB, member RAS oncogene family-like 3 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20200730 MGI PMID:32220963 1315051 Rabl3 RAB, member RAS oncogene family-like 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20200730 MGI PMID:32220963 1315051 Rabl3 RAB, member RAS oncogene family-like 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200730 MGI PMID:32220963 1315051 Rabl3 RAB, member RAS oncogene family-like 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200730 MGI PMID:32220963 1315055 Tent2 terminal nucleotidyltransferase 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17927953 1315059 Sh3yl1 Sh3 domain YSC-like 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20210121 MGI PMID:33086058 1315059 Sh3yl1 Sh3 domain YSC-like 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20210121 MGI PMID:33086058 1315059 Sh3yl1 Sh3 domain YSC-like 1 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20210121 MGI PMID:33086058 1315059 Sh3yl1 Sh3 domain YSC-like 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20210121 MGI PMID:33086058 1315059 Sh3yl1 Sh3 domain YSC-like 1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210121 MGI PMID:33086058 1315059 Sh3yl1 Sh3 domain YSC-like 1 gene MP:0011371 decreased kidney apoptosis IAGP N RGD:5509061 20210121 MGI PMID:33086058 1315059 Sh3yl1 Sh3 domain YSC-like 1 gene MP:0011372 decreased renal tubule apoptosis IAGP N RGD:5509061 20210121 MGI PMID:33086058 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19213845 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:19213845 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:19213845 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0001147 small testis IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:19213845 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:19213845 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19213845 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19213845 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20170713 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19213845 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20170713 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:19213845 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:19213845 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20150226 MGI PMID:23118208 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0003195 calcinosis IAGP N RGD:5509061 20141003 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0003196 calcified skin IAGP N RGD:5509061 20141003 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20170713 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0003199 calcified muscle IAGP N RGD:5509061 20170713 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20170713 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20170713 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19213845 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0010522 calcified aorta IAGP N RGD:5509061 20141003 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0010964 increased compact bone volume IAGP N RGD:5509061 20141003 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:19213845 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20170713 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0011585 decreased alkaline phosphatase activity IAGP N RGD:5509061 20170713 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0012337 increased vitamin D level IAGP N RGD:5509061 20170713 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20170713 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0031197 calcified testicular artery IAGP N RGD:5509061 20201119 MGI PMID:22912827 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315064 Galnt3 polypeptide N-acetylgalactosaminyltransferase 3 gene MP:0031355 abnormal proacrosomal vesicle fusion IAGP N RGD:5509061 20220407 MGI PMID:23052838 1315068 Tmprss11g transmembrane protease, serine 11g gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20191031 MGI PMID:31501243 1315070 Samd8 sterile alpha motif domain containing 8 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20170824 MGI PMID:25605874 1315070 Samd8 sterile alpha motif domain containing 8 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20170824 MGI PMID:25667419 1315070 Samd8 sterile alpha motif domain containing 8 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20170824 MGI PMID:25605874 1315070 Samd8 sterile alpha motif domain containing 8 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20170824 MGI PMID:25667419 1315070 Samd8 sterile alpha motif domain containing 8 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20170824 MGI PMID:25605874 1315070 Samd8 sterile alpha motif domain containing 8 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20170824 MGI PMID:25667419 1315073 Stk33 serine/threonine kinase 33 gene MP:0001925 male infertility IAGP N RGD:5509061 20191114 MGI PMID:29155043 1315073 Stk33 serine/threonine kinase 33 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20191114 MGI PMID:29155043 1315073 Stk33 serine/threonine kinase 33 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 1315073 Stk33 serine/threonine kinase 33 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20191114 MGI PMID:29155043 1315073 Stk33 serine/threonine kinase 33 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1315075 Psmd11 proteasome (prosome, macropain) 26S subunit, non-ATPase, 11 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240613 MGI PMID:33517884 1315075 Psmd11 proteasome (prosome, macropain) 26S subunit, non-ATPase, 11 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20240613 MGI PMID:33517884 1315075 Psmd11 proteasome (prosome, macropain) 26S subunit, non-ATPase, 11 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20240613 MGI PMID:33517884 1315075 Psmd11 proteasome (prosome, macropain) 26S subunit, non-ATPase, 11 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20240613 MGI PMID:33517884 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20160811 MGI 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11106738 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:11106738 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:23039116 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:23870400 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:23870400 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11106738 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:23039116 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11106738 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23870400 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21478856 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23754961 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11106738 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11106738 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21807948 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23754961 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23870400 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11106738 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:21807948 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:23754961 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:11106738 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:21807948 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:22549958 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:23754961 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:23754961 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11106738 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:23870400 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:11106738 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11106738 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20150212 MGI PMID:24532689 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:23870400 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0003572 abnormal uterus development IAGP N RGD:5509061 20141003 MGI PMID:23870400 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0004805 absent oocytes IAGP N RGD:5509061 20170601 MGI PMID:26742488 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:23039116 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0004952 increased spleen weight IEA N RGD:5509061 20220811 MGI 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:23870400 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005159 azoospermia IAGP N RGD:5509061 20170601 MGI PMID:26742488 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:11106738 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:21478856 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:21807948 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:23039116 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141030 MGI PMID:22530760 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18694567 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21478856 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21807948 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:22761591 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23318132 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141030 MGI PMID:22530760 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20150226 MGI PMID:24589552 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20201015 MGI PMID:32345962 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:21478856 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:22549958 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:23039116 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:11106738 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18694567 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23318132 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23870400 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20150226 MGI PMID:24589552 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20170601 MGI PMID:26742488 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20231123 MGI PMID:37891173 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141030 MGI PMID:22530760 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:23870400 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20150226 MGI PMID:24589552 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:21478856 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:21807948 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:23754961 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20150226 MGI PMID:24589552 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20170615 MGI PMID:27760146 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:23754961 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:23870400 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20150226 MGI PMID:24589552 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20170615 MGI PMID:27760146 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20210304 MGI PMID:30853435 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:11106739 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23754961 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23870400 1315082 Spo11 SPO11 initiator of meiotic double stranded breaks gene MP:0031474 increased female germ cell apoptosis IAGP N RGD:5509061 20230615 MGI PMID:21478856 1315085 Art4 ADP-ribosyltransferase 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1315085 Art4 ADP-ribosyltransferase 4 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1315088 Clstn1 calsyntenin 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20160421 MGI 1315088 Clstn1 calsyntenin 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20151022 MGI PMID:24966372 1315088 Clstn1 calsyntenin 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1315088 Clstn1 calsyntenin 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1315088 Clstn1 calsyntenin 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20210128 MGI 1315088 Clstn1 calsyntenin 1 gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20151022 MGI PMID:24966372 1315088 Clstn1 calsyntenin 1 gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20151022 MGI PMID:24966372 1315088 Clstn1 calsyntenin 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20151022 MGI PMID:24966372 1315088 Clstn1 calsyntenin 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20151022 MGI PMID:24966372 1315088 Clstn1 calsyntenin 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20151022 MGI PMID:24966372 1315088 Clstn1 calsyntenin 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20151022 MGI PMID:24966372 1315088 Clstn1 calsyntenin 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1315088 Clstn1 calsyntenin 1 gene MP:0011273 prolonged excitatory postsynaptic current decay time IAGP N RGD:5509061 20151022 MGI PMID:24966372 1315088 Clstn1 calsyntenin 1 gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:24966372 1315090 Cntnap4 contactin associated protein-like 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200521 MGI PMID:32194851 1315090 Cntnap4 contactin associated protein-like 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200521 MGI PMID:32194851 1315090 Cntnap4 contactin associated protein-like 4 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141009 MGI PMID:24870235 1315090 Cntnap4 contactin associated protein-like 4 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141009 MGI PMID:24870235 1315090 Cntnap4 contactin associated protein-like 4 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141009 MGI PMID:24870235 1315090 Cntnap4 contactin associated protein-like 4 gene MP:0002064 seizures IAGP N RGD:5509061 20141009 MGI PMID:24870235 1315090 Cntnap4 contactin associated protein-like 4 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141009 MGI PMID:24870235 1315090 Cntnap4 contactin associated protein-like 4 gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20141009 MGI PMID:24870235 1315090 Cntnap4 contactin associated protein-like 4 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20200521 MGI PMID:32194851 1315090 Cntnap4 contactin associated protein-like 4 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20141009 MGI PMID:24870235 1315090 Cntnap4 contactin associated protein-like 4 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141009 MGI PMID:24870235 1315090 Cntnap4 contactin associated protein-like 4 gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20200521 MGI PMID:32194851 1315090 Cntnap4 contactin associated protein-like 4 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20180301 MGI PMID:24870235 1315090 Cntnap4 contactin associated protein-like 4 gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20200521 MGI PMID:32194851 1315092 Gpr63 G protein-coupled receptor 63 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20231207 MGI 1315092 Gpr63 G protein-coupled receptor 63 gene MP:0000433 microcephaly IAGP N RGD:5509061 20200416 MGI PMID:31730647 1315092 Gpr63 G protein-coupled receptor 63 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200402 MGI PMID:31730647 1315092 Gpr63 G protein-coupled receptor 63 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20200402 MGI PMID:31730647 1315092 Gpr63 G protein-coupled receptor 63 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200402 MGI PMID:31730647 1315092 Gpr63 G protein-coupled receptor 63 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1315092 Gpr63 G protein-coupled receptor 63 gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20200402 MGI PMID:31730647 1315092 Gpr63 G protein-coupled receptor 63 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200402 MGI PMID:31730647 1315092 Gpr63 G protein-coupled receptor 63 gene MP:0012547 spina bifida cystica IAGP N RGD:5509061 20200402 MGI PMID:31730647 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21925315 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:21925315 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20200402 MGI 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20200402 MGI 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:21925315 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0003671 abnormal eyelid aperture IEA N RGD:5509061 20201231 MGI 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:21925315 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20200402 MGI 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20211021 MGI 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:21925315 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0010924 abnormal osteoid morphology IAGP N RGD:5509061 20141003 MGI PMID:21925315 1315094 Usp1 ubiquitin specific peptidase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19217432 1315095 Ttll8 tubulin tyrosine ligase-like family, member 8 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210422 MGI PMID:33414192 1315095 Ttll8 tubulin tyrosine ligase-like family, member 8 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210422 MGI PMID:33414192 1315095 Ttll8 tubulin tyrosine ligase-like family, member 8 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230119 MGI 1315095 Ttll8 tubulin tyrosine ligase-like family, member 8 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20210422 MGI PMID:33414192 1315095 Ttll8 tubulin tyrosine ligase-like family, member 8 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20210422 MGI PMID:33414192 1315095 Ttll8 tubulin tyrosine ligase-like family, member 8 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210422 MGI PMID:33414192 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0001712 abnormal placenta development IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0002861 abnormal tail bud morphology IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20221215 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1315098 Slc30a9 solute carrier family 30 (zinc transporter), member 9 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220811 MGI 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:13892780 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:5798244 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:11518730 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:11518730 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20150101 MGI PMID:17008558 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9680329 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12395314 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10225971 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9680329 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10225971 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11518730 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:9680329 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0002534 abnormal type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11518730 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0002534 abnormal type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:9680329 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20150101 MGI PMID:17008558 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20150101 MGI PMID:17008558 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:11518730 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20150101 MGI PMID:17008558 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20150101 MGI PMID:17008558 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:11518730 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20150101 MGI PMID:17008558 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10225971 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:13892780 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:17008558 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:5798244 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0020935 decreased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:13892780 1315100 Mst1r macrophage stimulating 1 receptor (c-met-related tyrosine kinase) gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:14505749 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17720808 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10669418 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17720808 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:12297047 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15294162 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17723215 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:16304053 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:17720808 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18250413 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12297047 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16304053 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17720808 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18412166 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16304053 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0002367 abnormal thymus lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:16304053 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10669418 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10669418 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16304053 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17720808 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:10669417 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:10669418 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17041586 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:18412166 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10669418 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15294162 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17720808 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:17720808 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:12297047 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18250413 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0004867 decreased platelet calcium level IAGP N RGD:5509061 20141003 MGI PMID:15705797 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16304053 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16304053 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17723215 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:18250413 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:17723215 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16304053 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17483449 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15294162 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17483449 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:15705797 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12297047 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20171116 MGI PMID:17499227 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:17723215 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17723215 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16304053 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16304053 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18250413 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17720808 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17723215 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:17720808 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17720808 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:10669418 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:15294162 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:17041586 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18412166 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10669416 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10669417 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10669418 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17041586 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17720808 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:18412166 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20170713 MGI PMID:25605974 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:15705797 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:19515725 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18250413 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0020928 increased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:18250413 1315104 Pik3cg phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201001 MGI PMID:15705797 1315108 Il19 interleukin 19 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20160512 MGI PMID:25794104 1315108 Il19 interleukin 19 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20160512 MGI PMID:25794104 1315108 Il19 interleukin 19 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20160512 MGI PMID:25794104 1315108 Il19 interleukin 19 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20160512 MGI PMID:25794104 1315108 Il19 interleukin 19 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20160512 MGI PMID:25794104 1315108 Il19 interleukin 19 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20160512 MGI PMID:25794104 1315108 Il19 interleukin 19 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20160512 MGI PMID:25794104 1315108 Il19 interleukin 19 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20160512 MGI PMID:25794104 1315108 Il19 interleukin 19 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20160512 MGI PMID:25794104 1315108 Il19 interleukin 19 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20160512 MGI PMID:25794104 1315108 Il19 interleukin 19 gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20160512 MGI PMID:25794104 1315108 Il19 interleukin 19 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160512 MGI PMID:25794104 1315111 Mtx2 metaxin 2 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210826 MGI 1315111 Mtx2 metaxin 2 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1315111 Mtx2 metaxin 2 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20240919 MGI 1315111 Mtx2 metaxin 2 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20240919 MGI 1315111 Mtx2 metaxin 2 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20240919 MGI 1315111 Mtx2 metaxin 2 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20240919 MGI 1315111 Mtx2 metaxin 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230601 MGI 1315111 Mtx2 metaxin 2 gene MP:0009331 absent primitive node IEA N RGD:5509061 20240919 MGI 1315111 Mtx2 metaxin 2 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1315111 Mtx2 metaxin 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315111 Mtx2 metaxin 2 gene MP:0012724 absent head fold IEA N RGD:5509061 20240919 MGI 1315111 Mtx2 metaxin 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 1315112 Lyz3 lysozyme 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230720 MGI 1315112 Lyz3 lysozyme 3 gene MP:0001257 increased body length IEA N RGD:5509061 20231207 MGI 1315112 Lyz3 lysozyme 3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230720 MGI 1315112 Lyz3 lysozyme 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230720 MGI 1315115 Rhbdd1 rhomboid domain containing 1 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20240404 MGI PMID:38453906 1315115 Rhbdd1 rhomboid domain containing 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20240404 MGI PMID:38453906 1315115 Rhbdd1 rhomboid domain containing 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20240404 MGI PMID:38453906 1315115 Rhbdd1 rhomboid domain containing 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20240404 MGI PMID:38453906 1315115 Rhbdd1 rhomboid domain containing 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20240404 MGI PMID:35436469 1315115 Rhbdd1 rhomboid domain containing 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20240404 MGI PMID:38453906 1315115 Rhbdd1 rhomboid domain containing 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20240404 MGI PMID:35436469 1315115 Rhbdd1 rhomboid domain containing 1 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20240404 MGI PMID:35436469 1315115 Rhbdd1 rhomboid domain containing 1 gene MP:0031265 increased susceptibility to hepatic steatosis IAGP N RGD:5509061 20240404 MGI PMID:35436469 1315117 Rab20 RAB20, member RAS oncogene family gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20180215 MGI PMID:28494243 1315117 Rab20 RAB20, member RAS oncogene family gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220811 MGI 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0000601 small liver IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0000692 small spleen IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0000706 small thymus IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0001263 weight loss IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0001785 edema IEA N RGD:5509061 20220519 MGI 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0001861 lung inflammation IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0001914 hemorrhage IEA N RGD:5509061 20220519 MGI 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0002083 premature death IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0003717 pallor IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0003846 matted coat IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20220519 MGI 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20240627 MGI PMID:38011999 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20240627 MGI PMID:38011999 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0011940 decreased food intake IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315119 Eif4b eukaryotic translation initiation factor 4B gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20211118 MGI PMID:34566982 1315123 Txk TXK tyrosine kinase gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:10213685 1315123 Txk TXK tyrosine kinase gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16860759 1315123 Txk TXK tyrosine kinase gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:10213685 1315123 Txk TXK tyrosine kinase gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10213685 1315123 Txk TXK tyrosine kinase gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16860759 1315123 Txk TXK tyrosine kinase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10213685 1315123 Txk TXK tyrosine kinase gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16860759 1315123 Txk TXK tyrosine kinase gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10213685 1315123 Txk TXK tyrosine kinase gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16860759 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20180809 MGI PMID:24549051 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20180809 MGI PMID:24549051 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180809 MGI PMID:24549051 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0001847 brain inflammation IAGP N RGD:5509061 20180809 MGI PMID:24549051 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180809 MGI PMID:24549051 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20180809 MGI PMID:24549051 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20180809 MGI PMID:24549051 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20180809 MGI PMID:24549051 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20180809 MGI PMID:24549051 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0004018 abnormal galactose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11286504 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0004018 abnormal galactose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8902187 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0004018 abnormal galactose homeostasis IAGP N RGD:5509061 20180809 MGI PMID:24549051 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20180809 MGI PMID:24549051 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180809 MGI PMID:24549051 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0011854 cerebral edema IAGP N RGD:5509061 20180809 MGI PMID:24549051 1315127 Galt galactose-1-phosphate uridyl transferase gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:24549051 1315130 Bcas2 BCAS2 pre-mRNA processing factor gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220519 MGI PMID:34972250 1315130 Bcas2 BCAS2 pre-mRNA processing factor gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20220519 MGI PMID:34972250 1315130 Bcas2 BCAS2 pre-mRNA processing factor gene MP:0001127 small ovary IAGP N RGD:5509061 20220519 MGI PMID:34972250 1315130 Bcas2 BCAS2 pre-mRNA processing factor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220519 MGI PMID:34972250 1315130 Bcas2 BCAS2 pre-mRNA processing factor gene MP:0001926 female infertility IAGP N RGD:5509061 20171005 MGI PMID:26428007 1315130 Bcas2 BCAS2 pre-mRNA processing factor gene MP:0001926 female infertility IAGP N RGD:5509061 20220519 MGI PMID:34972250 1315130 Bcas2 BCAS2 pre-mRNA processing factor gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20220519 MGI PMID:34972250 1315130 Bcas2 BCAS2 pre-mRNA processing factor gene MP:0003718 maternal effect IAGP N RGD:5509061 20171005 MGI PMID:26428007 1315130 Bcas2 BCAS2 pre-mRNA processing factor gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20220519 MGI PMID:34972250 1315130 Bcas2 BCAS2 pre-mRNA processing factor gene MP:0011124 increased primary ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:34972250 1315130 Bcas2 BCAS2 pre-mRNA processing factor gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:34972250 1315130 Bcas2 BCAS2 pre-mRNA processing factor gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20171005 MGI PMID:26428007 1315130 Bcas2 BCAS2 pre-mRNA processing factor gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:34972250 1315130 Bcas2 BCAS2 pre-mRNA processing factor gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:34972250 1315132 Habp4 hyaluronic acid binding protein 4 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20211014 MGI PMID:33245729 1315132 Habp4 hyaluronic acid binding protein 4 gene MP:0014201 abnormal intestinal epithelium physiology IAGP N RGD:5509061 20211014 MGI PMID:33245729 1315133 Rab3gap1 RAB3 GTPase activating protein subunit 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1315133 Rab3gap1 RAB3 GTPase activating protein subunit 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1315133 Rab3gap1 RAB3 GTPase activating protein subunit 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16782817 1315133 Rab3gap1 RAB3 GTPase activating protein subunit 1 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:16782817 1315133 Rab3gap1 RAB3 GTPase activating protein subunit 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1315133 Rab3gap1 RAB3 GTPase activating protein subunit 1 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:16782817 1315133 Rab3gap1 RAB3 GTPase activating protein subunit 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1315133 Rab3gap1 RAB3 GTPase activating protein subunit 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 1315135 Appbp2 amyloid beta precursor protein binding protein 2 gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20201022 MGI 1315135 Appbp2 amyloid beta precursor protein binding protein 2 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201022 MGI 1315135 Appbp2 amyloid beta precursor protein binding protein 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1315135 Appbp2 amyloid beta precursor protein binding protein 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1315135 Appbp2 amyloid beta precursor protein binding protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1315137 Rab5b RAB5B, member RAS oncogene family gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 1315137 Rab5b RAB5B, member RAS oncogene family gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220811 MGI 1315137 Rab5b RAB5B, member RAS oncogene family gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1315141 Nin ninein gene MP:0001199 thin skin IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0001218 thin epidermis IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0001238 thin epidermis stratum spinosum IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210128 MGI 1315141 Nin ninein gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1315141 Nin ninein gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20170105 MGI 1315141 Nin ninein gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1315141 Nin ninein gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20170105 MGI 1315141 Nin ninein gene MP:0009441 delayed skin barrier formation IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0009598 thin epidermis stratum granulosum IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0009605 decreased keratohyalin granule number IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0009607 decreased keratohyalin granule size IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0009714 thin epidermis stratum basale IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315141 Nin ninein gene MP:0030605 abnormal corneocyte morphology IAGP N RGD:5509061 20190919 MGI PMID:30923192 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220519 MGI 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20220519 MGI 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20240321 MGI PMID:37228654 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20240321 MGI PMID:37228654 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20220519 MGI 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0001785 edema IAGP N RGD:5509061 20240321 MGI PMID:37228654 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20240321 MGI PMID:37228654 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20220519 MGI 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20240321 MGI PMID:37228654 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20240321 MGI PMID:37228654 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20240321 MGI PMID:37228654 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20240321 MGI PMID:37228654 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20240321 MGI PMID:37228654 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0012270 cardiac edema IAGP N RGD:5509061 20240321 MGI PMID:37228654 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20240321 MGI PMID:37228654 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220519 MGI 1315142 Dync2i1 dynein 2 intermediate chain 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1315143 Vopp1 vesicular, overexpressed in cancer, prosurvival protein 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20201231 MGI 1315143 Vopp1 vesicular, overexpressed in cancer, prosurvival protein 1 gene MP:0002546 mydriasis IEA N RGD:5509061 20240523 MGI 1315143 Vopp1 vesicular, overexpressed in cancer, prosurvival protein 1 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20181227 MGI 1315143 Vopp1 vesicular, overexpressed in cancer, prosurvival protein 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1315146 Rad1 RAD1 checkpoint DNA exonuclease gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1315146 Rad1 RAD1 checkpoint DNA exonuclease gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1315146 Rad1 RAD1 checkpoint DNA exonuclease gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20181227 MGI 1315146 Rad1 RAD1 checkpoint DNA exonuclease gene MP:0002608 increased hematocrit IEA N RGD:5509061 20231207 MGI 1315146 Rad1 RAD1 checkpoint DNA exonuclease gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20210520 MGI 1315146 Rad1 RAD1 checkpoint DNA exonuclease gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1315146 Rad1 RAD1 checkpoint DNA exonuclease gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220519 MGI 1315146 Rad1 RAD1 checkpoint DNA exonuclease gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220519 MGI 1315146 Rad1 RAD1 checkpoint DNA exonuclease gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315146 Rad1 RAD1 checkpoint DNA exonuclease gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1315146 Rad1 RAD1 checkpoint DNA exonuclease gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1315152 Knop1 lysine rich nucleolar protein 1 gene MP:0000745 tremors IEA N RGD:5509061 20190502 MGI 1315152 Knop1 lysine rich nucleolar protein 1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20210128 MGI 1315152 Knop1 lysine rich nucleolar protein 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20220811 MGI 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0005380 embryo phenotype IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0005387 immune system phenotype IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0008651 increased interleukin-1 secretion IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315156 Socs4 suppressor of cytokine signaling 4 gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20240229 MGI PMID:24809749 1315158 Klhdc2 kelch domain containing 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1315158 Klhdc2 kelch domain containing 2 gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20160421 MGI 1315158 Klhdc2 kelch domain containing 2 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20160421 MGI 1315158 Klhdc2 kelch domain containing 2 gene MP:0000745 tremors IEA N RGD:5509061 20141003 MGI 1315158 Klhdc2 kelch domain containing 2 gene MP:0001260 increased body weight IEA N RGD:5509061 20141003 MGI 1315158 Klhdc2 kelch domain containing 2 gene MP:0001314 cornea opacity IEA N RGD:5509061 20141003 MGI 1315158 Klhdc2 kelch domain containing 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20141003 MGI 1315158 Klhdc2 kelch domain containing 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20170105 MGI 1315158 Klhdc2 kelch domain containing 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1315158 Klhdc2 kelch domain containing 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1315158 Klhdc2 kelch domain containing 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1315158 Klhdc2 kelch domain containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315162 Rad54b RAD54 homolog B (S. cerevisiae) gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:16428451 1315162 Rad54b RAD54 homolog B (S. cerevisiae) gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16428451 1315162 Rad54b RAD54 homolog B (S. cerevisiae) gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16428451 1315162 Rad54b RAD54 homolog B (S. cerevisiae) gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16428451 1315164 Erlec1 endoplasmic reticulum lectin 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1315164 Erlec1 endoplasmic reticulum lectin 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1315164 Erlec1 endoplasmic reticulum lectin 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1315164 Erlec1 endoplasmic reticulum lectin 1 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20191128 MGI 1315164 Erlec1 endoplasmic reticulum lectin 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20221215 MGI 1315166 Ruvbl2 RuvB-like AAA ATPase 2 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:22761313 1315166 Ruvbl2 RuvB-like AAA ATPase 2 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1315166 Ruvbl2 RuvB-like AAA ATPase 2 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241017 MGI 1315166 Ruvbl2 RuvB-like AAA ATPase 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1315166 Ruvbl2 RuvB-like AAA ATPase 2 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1315166 Ruvbl2 RuvB-like AAA ATPase 2 gene MP:0002718 abnormal inner cell mass morphology IEA N RGD:5509061 20241017 MGI 1315166 Ruvbl2 RuvB-like AAA ATPase 2 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22761313 1315166 Ruvbl2 RuvB-like AAA ATPase 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1315166 Ruvbl2 RuvB-like AAA ATPase 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1315166 Ruvbl2 RuvB-like AAA ATPase 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1315166 Ruvbl2 RuvB-like AAA ATPase 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1315166 Ruvbl2 RuvB-like AAA ATPase 2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1315166 Ruvbl2 RuvB-like AAA ATPase 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1315166 Ruvbl2 RuvB-like AAA ATPase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1315166 Ruvbl2 RuvB-like AAA ATPase 2 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22761313 1315170 Hoxd10 homeobox D10 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:12869760 1315170 Hoxd10 homeobox D10 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9409668 1315170 Hoxd10 homeobox D10 gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:9409668 1315170 Hoxd10 homeobox D10 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9409668 1315170 Hoxd10 homeobox D10 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:17626057 1315170 Hoxd10 homeobox D10 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9409668 1315170 Hoxd10 homeobox D10 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1315170 Hoxd10 homeobox D10 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1315170 Hoxd10 homeobox D10 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1315170 Hoxd10 homeobox D10 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9409668 1315170 Hoxd10 homeobox D10 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:12869760 1315170 Hoxd10 homeobox D10 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:9409668 1315170 Hoxd10 homeobox D10 gene MP:0003854 abnormal forelimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1315170 Hoxd10 homeobox D10 gene MP:0003856 abnormal hindlimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1315170 Hoxd10 homeobox D10 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:12869760 1315170 Hoxd10 homeobox D10 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:12869760 1315170 Hoxd10 homeobox D10 gene MP:0004600 abnormal vertebral transverse process morphology IAGP N RGD:5509061 20141003 MGI PMID:9409668 1315170 Hoxd10 homeobox D10 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12869760 1315170 Hoxd10 homeobox D10 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12869760 1315170 Hoxd10 homeobox D10 gene MP:0004622 sacral vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0004622 sacral vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:9409668 1315170 Hoxd10 homeobox D10 gene MP:0004654 absent lumbar vertebrae IAGP N RGD:5509061 20141003 MGI PMID:12869760 1315170 Hoxd10 homeobox D10 gene MP:0004694 absent patella IAGP N RGD:5509061 20141003 MGI PMID:12869760 1315170 Hoxd10 homeobox D10 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0005353 abnormal patella morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0005353 abnormal patella morphology IAGP N RGD:5509061 20141003 MGI PMID:9409668 1315170 Hoxd10 homeobox D10 gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0009005 abnormal sesamoid bone of gastrocnemius morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315170 Hoxd10 homeobox D10 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:10642795 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0001260 increased body weight IAGP N RGD:5509061 20180111 MGI PMID:24072708 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20180111 MGI PMID:24072708 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20180111 MGI PMID:24072708 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20180111 MGI PMID:24072708 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20180111 MGI PMID:24072708 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20180111 MGI PMID:24072708 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20180111 MGI PMID:24072708 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0011016 increased core body temperature IAGP N RGD:5509061 20180111 MGI PMID:24072708 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0011019 abnormal adaptive thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:24072708 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20180111 MGI PMID:24072708 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0011939 increased food intake IAGP N RGD:5509061 20180111 MGI PMID:24072708 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20180111 MGI PMID:24072708 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0014476 abnormal feces lipid level IAGP N RGD:5509061 20240704 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20160421 MGI PMID:22345407 1315173 Acot13 acyl-CoA thioesterase 13 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:22345407 1315175 Capn15 calpain 15 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210121 MGI PMID:32885237 1315175 Capn15 calpain 15 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20210121 MGI PMID:32885237 1315175 Capn15 calpain 15 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20210121 MGI PMID:32885237 1315175 Capn15 calpain 15 gene MP:0001304 cataract IAGP N RGD:5509061 20210121 MGI PMID:32885237 1315175 Capn15 calpain 15 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210121 MGI PMID:32885237 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:24143185 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:24143185 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:12766770 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:22730198 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:23469164 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:24143185 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:15838507 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:22730198 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:12766770 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:15838507 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000576 clubfoot IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0000592 short tail IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:15623520 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:15623520 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0001195 flaky skin IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:12766770 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:22730198 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:24143185 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0001208 blistering IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20111116 MGI 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:23469164 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22730198 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20111116 MGI 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0002639 micrognathia IEA N RGD:5509061 20150903 MGI 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:24143185 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15623520 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:15623520 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:24143185 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0005242 cryptophthalmos IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0005242 cryptophthalmos IAGP N RGD:5509061 20141003 MGI PMID:12766770 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0005242 cryptophthalmos IAGP N RGD:5509061 20141003 MGI PMID:15838507 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:22730198 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:24143185 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:22730198 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15623520 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0008854 bleb IAGP N RGD:5509061 20141003 MGI PMID:23469164 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0008854 bleb IAGP N RGD:5509061 20141003 MGI PMID:24143185 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0008856 fetal bleb IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0008856 fetal bleb IAGP N RGD:5509061 20141003 MGI PMID:15838507 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:23469164 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:24143185 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0009874 abnormal interdigital cell death IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:24143185 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:23469164 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:24143185 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20150903 MGI 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0010977 fused right lung lobes IAGP N RGD:5509061 20141003 MGI PMID:15623520 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12766770 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15838507 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12766770 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:22730198 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:22730198 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0011364 abnormal metanephros morphology IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12766769 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0011499 abnormal glomerular capsule space morphology IAGP N RGD:5509061 20141003 MGI PMID:22730198 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0013177 abnormal tail tip morphology IAGP N RGD:5509061 20221201 MGI PMID:26813283 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:24143185 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0031152 subcutaneous hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:24143185 1315179 Fras1 Fraser extracellular matrix complex subunit 1 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:24143185 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0000561 adactyly IAGP N RGD:5509061 20141003 MGI PMID:9733575 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:10471509 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:8666395 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:9733575 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:9733575 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0001677 absent apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:9733575 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0001679 thin apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:9733575 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0004576 abnormal embryonic autopod plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9733575 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0005109 abnormal talus morphology IAGP N RGD:5509061 20141003 MGI PMID:9733575 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0005230 ectrodactyly IAGP N RGD:5509061 20141003 MGI PMID:10471509 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0005230 ectrodactyly IAGP N RGD:5509061 20141003 MGI PMID:8666395 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0005230 ectrodactyly IAGP N RGD:5509061 20141003 MGI PMID:9733575 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:9733575 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:9733575 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:9733575 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9733575 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10471509 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8666395 1315183 Fbxw4 F-box and WD-40 domain protein 4 gene MP:0014291 decreased autopod size IAGP N RGD:5509061 20230824 MGI PMID:9733575 1315186 Efl1 elongation factor like GTPase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160929 MGI PMID:27534441 1315186 Efl1 elongation factor like GTPase 1 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20241010 MGI 1315186 Efl1 elongation factor like GTPase 1 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20241010 MGI 1315186 Efl1 elongation factor like GTPase 1 gene MP:0002582 disorganized extraembryonic tissue IEA N RGD:5509061 20241010 MGI 1315186 Efl1 elongation factor like GTPase 1 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20241010 MGI 1315186 Efl1 elongation factor like GTPase 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241010 MGI 1315186 Efl1 elongation factor like GTPase 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1315186 Efl1 elongation factor like GTPase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315188 Rgs18 regulator of G-protein signaling 18 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20160324 MGI PMID:25405900 1315188 Rgs18 regulator of G-protein signaling 18 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20160324 MGI PMID:25405900 1315188 Rgs18 regulator of G-protein signaling 18 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20160324 MGI PMID:25405900 1315188 Rgs18 regulator of G-protein signaling 18 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20160324 MGI PMID:25405900 1315188 Rgs18 regulator of G-protein signaling 18 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20160324 MGI PMID:25405900 1315188 Rgs18 regulator of G-protein signaling 18 gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20160324 MGI PMID:25969426 1315188 Rgs18 regulator of G-protein signaling 18 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20160324 MGI PMID:25405900 1315188 Rgs18 regulator of G-protein signaling 18 gene MP:0009586 increased platelet aggregation IAGP N RGD:5509061 20160324 MGI PMID:25405900 1315188 Rgs18 regulator of G-protein signaling 18 gene MP:0009586 increased platelet aggregation IAGP N RGD:5509061 20160324 MGI PMID:25969426 1315188 Rgs18 regulator of G-protein signaling 18 gene MP:0009676 abnormal hemostasis IAGP N RGD:5509061 20160324 MGI PMID:25969426 1315188 Rgs18 regulator of G-protein signaling 18 gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:25969426 1315191 Etv4 ets variant 4 gene MP:0000413 polyphalangy IAGP N RGD:5509061 20141003 MGI PMID:19386269 1315191 Etv4 ets variant 4 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:19898483 1315191 Etv4 ets variant 4 gene MP:0000524 decreased renal tubule number IAGP N RGD:5509061 20141003 MGI PMID:19898483 1315191 Etv4 ets variant 4 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19386269 1315191 Etv4 ets variant 4 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:14635793 1315191 Etv4 ets variant 4 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12372283 1315191 Etv4 ets variant 4 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:12372283 1315191 Etv4 ets variant 4 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12372283 1315191 Etv4 ets variant 4 gene MP:0000959 abnormal somatic sensory system morphology IAGP N RGD:5509061 20141003 MGI PMID:16493690 1315191 Etv4 ets variant 4 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:23522042 1315191 Etv4 ets variant 4 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:12372283 1315191 Etv4 ets variant 4 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:14635793 1315191 Etv4 ets variant 4 gene MP:0001378 abnormal ejaculation IAGP N RGD:5509061 20141003 MGI PMID:11094084 1315191 Etv4 ets variant 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1315191 Etv4 ets variant 4 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:12372283 1315191 Etv4 ets variant 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11094084 1315191 Etv4 ets variant 4 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19898483 1315191 Etv4 ets variant 4 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19898483 1315191 Etv4 ets variant 4 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:19898483 1315191 Etv4 ets variant 4 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:19898483 1315191 Etv4 ets variant 4 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:19898483 1315191 Etv4 ets variant 4 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:19898483 1315191 Etv4 ets variant 4 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23522042 1315191 Etv4 ets variant 4 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:19898483 1315191 Etv4 ets variant 4 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:19386269 1315191 Etv4 ets variant 4 gene MP:0008486 decreased muscle spindle number IAGP N RGD:5509061 20141003 MGI PMID:23522042 1315191 Etv4 ets variant 4 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19386269 1315191 Etv4 ets variant 4 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14635793 1315191 Etv4 ets variant 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19386269 1315191 Etv4 ets variant 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19386269 1315191 Etv4 ets variant 4 gene MP:0030996 decreased pacinian corpuscle number IAGP N RGD:5509061 20200130 MGI PMID:16493690 1315191 Etv4 ets variant 4 gene MP:0030998 small pacinian corpuscles IAGP N RGD:5509061 20200130 MGI PMID:16493690 1315193 Mlana melan-A gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:21943097 1315193 Mlana melan-A gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:21943097 1315193 Mlana melan-A gene MP:0001189 absent skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21943097 1315193 Mlana melan-A gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21943097 1315194 Inka2 inka box actin regulator 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20230323 MGI PMID:36301793 1315194 Inka2 inka box actin regulator 2 gene MP:0020337 abnormal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20230323 MGI PMID:36301793 1315194 Inka2 inka box actin regulator 2 gene MP:0021018 decreased dendritic spine number IAGP N RGD:5509061 20230323 MGI PMID:36301793 1315194 Inka2 inka box actin regulator 2 gene MP:0021090 abnormal dendrite arborization pattern IAGP N RGD:5509061 20230323 MGI PMID:36301793 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14684813 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210617 MGI PMID:33524375 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14684813 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14684813 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14684813 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14684813 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14684813 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20210617 MGI PMID:33524375 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20210617 MGI PMID:33524375 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14684813 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20210701 MGI PMID:33524375 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:14684813 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0008903 abnormal mesenteric fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:14684813 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20210617 MGI PMID:33524375 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210617 MGI PMID:33524375 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14684813 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0012224 abnormal sterol level IAGP N RGD:5509061 20210617 MGI PMID:33524375 1315198 Dhcr24 24-dehydrocholesterol reductase gene MP:0013600 testis degeneration IAGP N RGD:5509061 20150312 MGI PMID:14684813 1315200 Krt34 keratin 34 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1315200 Krt34 keratin 34 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1315200 Krt34 keratin 34 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1315200 Krt34 keratin 34 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1315200 Krt34 keratin 34 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1315200 Krt34 keratin 34 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1315200 Krt34 keratin 34 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1315200 Krt34 keratin 34 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1315200 Krt34 keratin 34 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1315200 Krt34 keratin 34 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1315200 Krt34 keratin 34 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20240523 MGI 1315200 Krt34 keratin 34 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20240523 MGI 1315200 Krt34 keratin 34 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1315202 Ndst4 N-deacetylase/N-sulfotransferase (heparin glucosaminyl) 4 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20180301 MGI PMID:27793051 1315202 Ndst4 N-deacetylase/N-sulfotransferase (heparin glucosaminyl) 4 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20180301 MGI PMID:27793051 1315202 Ndst4 N-deacetylase/N-sulfotransferase (heparin glucosaminyl) 4 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20180301 MGI PMID:27793051 1315202 Ndst4 N-deacetylase/N-sulfotransferase (heparin glucosaminyl) 4 gene MP:0014221 increased colon goblet cell number IAGP N RGD:5509061 20180301 MGI PMID:27793051 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16243035 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:16243035 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18334636 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16243035 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18334636 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160908 MGI PMID:26621702 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160908 MGI PMID:26621702 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18334636 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18334636 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:18334636 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20160908 MGI PMID:26621702 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20160908 MGI PMID:26621702 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20160908 MGI PMID:26621702 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:18334636 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20160908 MGI PMID:26621702 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18334636 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:16243035 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:16243035 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:16243036 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20160908 MGI PMID:26621702 1315206 Prex1 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:26621702 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0000692 small spleen IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0001262 decreased body weight IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0002764 short tibia IEA N RGD:5509061 20231207 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20240523 MGI 1315208 Dcaf5 DDB1 and CUL4 associated factor 5 gene MP:0011044 increased lung elastance IEA N RGD:5509061 20240523 MGI 1315211 Orai3 ORAI calcium release-activated calcium modulator 3 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20240516 MGI PMID:36803766 1315211 Orai3 ORAI calcium release-activated calcium modulator 3 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1315211 Orai3 ORAI calcium release-activated calcium modulator 3 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20240516 MGI PMID:36803766 1315211 Orai3 ORAI calcium release-activated calcium modulator 3 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20240516 MGI PMID:36803766 1315211 Orai3 ORAI calcium release-activated calcium modulator 3 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20240516 MGI PMID:36803766 1315212 Scara5 scavenger receptor class A, member 5 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:23499552 1315212 Scara5 scavenger receptor class A, member 5 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:23499552 1315212 Scara5 scavenger receptor class A, member 5 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23499552 1315212 Scara5 scavenger receptor class A, member 5 gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:23499552 1315212 Scara5 scavenger receptor class A, member 5 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23499552 1315212 Scara5 scavenger receptor class A, member 5 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:23499552 1315212 Scara5 scavenger receptor class A, member 5 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:23499552 1315212 Scara5 scavenger receptor class A, member 5 gene MP:0009646 urinary bladder inflammation IAGP N RGD:5509061 20141003 MGI PMID:23499552 1315212 Scara5 scavenger receptor class A, member 5 gene MP:0020386 adipose tissue inflammation IAGP N RGD:5509061 20161117 MGI PMID:23499552 1315221 Wdr35 WD repeat domain 35 gene MP:0000151 absent ribs IAGP N RGD:5509061 20141003 MGI PMID:21473986 1315221 Wdr35 WD repeat domain 35 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21473986 1315221 Wdr35 WD repeat domain 35 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21473986 1315221 Wdr35 WD repeat domain 35 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:21473986 1315221 Wdr35 WD repeat domain 35 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21473986 1315221 Wdr35 WD repeat domain 35 gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:21473986 1315221 Wdr35 WD repeat domain 35 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:21473986 1315221 Wdr35 WD repeat domain 35 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20141003 MGI PMID:21473986 1315221 Wdr35 WD repeat domain 35 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:21473986 1315221 Wdr35 WD repeat domain 35 gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:21473986 1315221 Wdr35 WD repeat domain 35 gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:21473986 1315221 Wdr35 WD repeat domain 35 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:21473986 1315221 Wdr35 WD repeat domain 35 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:21473986 1315221 Wdr35 WD repeat domain 35 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:21473986 1315221 Wdr35 WD repeat domain 35 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21473986 1315224 Myef2 myelin basic protein expression factor 2, repressor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200514 MGI 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20201022 MGI 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:23200860 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20181227 MGI 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23200860 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23200860 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23200860 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20141003 MGI PMID:23200860 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:23200860 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:23200860 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:23200860 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23200860 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23200860 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23200860 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23200860 1315226 Stard10 StAR related lipid transfer domain containing 10 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:23200860 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20829512 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170209 MGI 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23592719 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0000445 short snout IEA N RGD:5509061 20170209 MGI 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20170209 MGI 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:20829512 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23592719 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:20829512 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20829512 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20170209 MGI 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23592719 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0002192 hydrops fetalis IEA N RGD:5509061 20170209 MGI 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20170209 MGI 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0002639 micrognathia IEA N RGD:5509061 20170209 MGI 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23592719 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:20829512 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23592719 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0006130 pulmonary valve atresia IEA N RGD:5509061 20170209 MGI 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:23592719 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23592719 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20829512 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20170209 MGI 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0010428 abnormal heart right ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:20829512 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0010617 thick mitral valve cusps IAGP N RGD:5509061 20141003 MGI PMID:20829512 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20829512 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315228 Dock1 dedicator of cytokinesis 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20829512 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21298075 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20221117 MGI PMID:23543054 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20221117 MGI PMID:23543054 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21298075 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21298075 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:21298075 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0001967 deafness IAGP N RGD:5509061 20221117 MGI PMID:23543054 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19936227 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0003100 myopia IAGP N RGD:5509061 20221117 MGI PMID:23543054 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0003986 small cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:19936227 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:19936227 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:19936227 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0004409 abnormal crista ampullaris neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19936227 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0004632 abnormal cochlear OHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:19936227 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0004633 abnormal cochlear IHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:19936227 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0004746 abnormal cochlear IHC afferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:19936227 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19936227 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:21298075 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0011041 abnormal vertical vestibuloocular reflex IAGP N RGD:5509061 20141003 MGI PMID:21298075 1315230 Slitrk6 SLIT and NTRK-like family, member 6 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21298075 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20160811 MGI 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0000603 pale liver IEA N RGD:5509061 20210520 MGI 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20201022 MGI 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20181227 MGI 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20160811 MGI 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0008480 absent eye pigmentation IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0020389 increased radial glial cell number IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315232 Bloc1s2 biogenesis of lysosomal organelles complex-1, subunit 2 gene MP:0020393 increased neuronal precursor proliferation IAGP N RGD:5509061 20170518 MGI PMID:27719760 1315234 Slc2a10 solute carrier family 2 (facilitated glucose transporter), member 10 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:19028722 1315234 Slc2a10 solute carrier family 2 (facilitated glucose transporter), member 10 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19028722 1315234 Slc2a10 solute carrier family 2 (facilitated glucose transporter), member 10 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:19028722 1315234 Slc2a10 solute carrier family 2 (facilitated glucose transporter), member 10 gene MP:0002964 aortic elastic tissue lesions IAGP N RGD:5509061 20141003 MGI PMID:19028722 1315234 Slc2a10 solute carrier family 2 (facilitated glucose transporter), member 10 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19028722 1315234 Slc2a10 solute carrier family 2 (facilitated glucose transporter), member 10 gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19028722 1315234 Slc2a10 solute carrier family 2 (facilitated glucose transporter), member 10 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19028722 1315234 Slc2a10 solute carrier family 2 (facilitated glucose transporter), member 10 gene MP:0006083 abnormal blood vessel elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:19028722 1315234 Slc2a10 solute carrier family 2 (facilitated glucose transporter), member 10 gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:19028722 1315234 Slc2a10 solute carrier family 2 (facilitated glucose transporter), member 10 gene MP:0009869 abnormal descending aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:19028722 1315234 Slc2a10 solute carrier family 2 (facilitated glucose transporter), member 10 gene MP:0010903 abnormal pulmonary alveolus wall morphology IAGP N RGD:5509061 20141003 MGI PMID:19028722 1315234 Slc2a10 solute carrier family 2 (facilitated glucose transporter), member 10 gene MP:0011309 abnormal kidney arterial blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19028722 1315236 Armc5 armadillo repeat containing 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180607 MGI PMID:28911199 1315236 Armc5 armadillo repeat containing 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180607 MGI PMID:28911199 1315236 Armc5 armadillo repeat containing 5 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20180607 MGI PMID:28911199 1315236 Armc5 armadillo repeat containing 5 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20180607 MGI PMID:28911199 1315236 Armc5 armadillo repeat containing 5 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20180607 MGI PMID:28911199 1315236 Armc5 armadillo repeat containing 5 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20180607 MGI PMID:28911199 1315236 Armc5 armadillo repeat containing 5 gene MP:0005129 increased adrenocorticotropin level IAGP N RGD:5509061 20180607 MGI PMID:28911199 1315236 Armc5 armadillo repeat containing 5 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20180607 MGI PMID:28911199 1315236 Armc5 armadillo repeat containing 5 gene MP:0008294 abnormal adrenal gland zona fasciculata morphology IAGP N RGD:5509061 20180607 MGI PMID:28911199 1315236 Armc5 armadillo repeat containing 5 gene MP:0008302 thin adrenal cortex IAGP N RGD:5509061 20180607 MGI PMID:28911199 1315236 Armc5 armadillo repeat containing 5 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20180607 MGI PMID:28911199 1315236 Armc5 armadillo repeat containing 5 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180607 MGI PMID:28911199 1315238 Xpr1 xenotropic and polytropic retrovirus receptor 1 gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:2991590 1315241 2900026A02Rik RIKEN cDNA 2900026A02 gene gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20141003 MGI 1315241 2900026A02Rik RIKEN cDNA 2900026A02 gene gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20141003 MGI 1315247 Il17ra interleukin 17 receptor A gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11514607 1315247 Il17ra interleukin 17 receptor A gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1315247 Il17ra interleukin 17 receptor A gene MP:0000601 small liver IEA N RGD:5509061 20230119 MGI 1315247 Il17ra interleukin 17 receptor A gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230119 MGI 1315247 Il17ra interleukin 17 receptor A gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20230119 MGI 1315247 Il17ra interleukin 17 receptor A gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:22951726 1315247 Il17ra interleukin 17 receptor A gene MP:0001406 abnormal gait IEA N RGD:5509061 20231207 MGI 1315247 Il17ra interleukin 17 receptor A gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1315247 Il17ra interleukin 17 receptor A gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18768888 1315247 Il17ra interleukin 17 receptor A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1315247 Il17ra interleukin 17 receptor A gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:11514607 1315247 Il17ra interleukin 17 receptor A gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230601 MGI 1315247 Il17ra interleukin 17 receptor A gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23034650 1315247 Il17ra interleukin 17 receptor A gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:11514607 1315247 Il17ra interleukin 17 receptor A gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:22951726 1315247 Il17ra interleukin 17 receptor A gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22951726 1315247 Il17ra interleukin 17 receptor A gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20154671 1315247 Il17ra interleukin 17 receptor A gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:11514607 1315247 Il17ra interleukin 17 receptor A gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22951726 1315247 Il17ra interleukin 17 receptor A gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:22951726 1315247 Il17ra interleukin 17 receptor A gene MP:0008671 abnormal interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:18768888 1315247 Il17ra interleukin 17 receptor A gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:22951726 1315247 Il17ra interleukin 17 receptor A gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:21982598 1315247 Il17ra interleukin 17 receptor A gene MP:0008701 abnormal interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:18768888 1315247 Il17ra interleukin 17 receptor A gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:22951726 1315247 Il17ra interleukin 17 receptor A gene MP:0008712 decreased interleukin-9 secretion IAGP N RGD:5509061 20141003 MGI PMID:20154671 1315247 Il17ra interleukin 17 receptor A gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:11514607 1315247 Il17ra interleukin 17 receptor A gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18411338 1315247 Il17ra interleukin 17 receptor A gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 1315247 Il17ra interleukin 17 receptor A gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20240523 MGI 1315247 Il17ra interleukin 17 receptor A gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:22951726 1315249 Rem1 rad and gem related GTP binding protein 1 gene MP:0020346 abnormal myocardial fiber calcium currents IAGP N RGD:5509061 20230223 MGI PMID:22854599 1315253 Ftmt ferritin mitochondrial gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1315255 Dst dystonin gene MP:0000333 decreased bone marrow cell number IEA N RGD:5509061 20111116 MGI 1315255 Dst dystonin gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:7736575 1315255 Dst dystonin gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:7736575 1315255 Dst dystonin gene MP:0000743 muscle spasm IEA N RGD:5509061 20111116 MGI 1315255 Dst dystonin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16087202 1315255 Dst dystonin gene MP:0000746 weakness IEA N RGD:5509061 20111116 MGI 1315255 Dst dystonin gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:10357897 1315255 Dst dystonin gene MP:0000754 paresis IEA N RGD:5509061 20111116 MGI 1315255 Dst dystonin gene MP:0000774 decreased brain size IAGP N RGD:5509061 20160304 MGI PMID:25195653 1315255 Dst dystonin gene MP:0000911 abnormal trigeminal motor nucleus morphology IAGP N RGD:5509061 20160304 MGI PMID:25195653 1315255 Dst dystonin gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:3138544 1315255 Dst dystonin gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:9570777 1315255 Dst dystonin gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:12859670 1315255 Dst dystonin gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:7217981 1315255 Dst dystonin gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:9570777 1315255 Dst dystonin gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:9618216 1315255 Dst dystonin gene MP:0000921 demyelination IAGP N RGD:5509061 20160304 MGI PMID:25195653 1315255 Dst dystonin gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0000958 peripheral nervous system degeneration IAGP N RGD:5509061 20141003 MGI PMID:9581287 1315255 Dst dystonin gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12859670 1315255 Dst dystonin gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:24381311 1315255 Dst dystonin gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9618216 1315255 Dst dystonin gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:24381311 1315255 Dst dystonin gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20160304 MGI PMID:25195653 1315255 Dst dystonin gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:24381311 1315255 Dst dystonin gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9581287 1315255 Dst dystonin gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:24381311 1315255 Dst dystonin gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16289886 1315255 Dst dystonin gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16289886 1315255 Dst dystonin gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9570777 1315255 Dst dystonin gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:7736575 1315255 Dst dystonin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16087202 1315255 Dst dystonin gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1315255 Dst dystonin gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 1315255 Dst dystonin gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20141003 MGI PMID:16087202 1315255 Dst dystonin gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:24381311 1315255 Dst dystonin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16087202 1315255 Dst dystonin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16087202 1315255 Dst dystonin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:24381311 1315255 Dst dystonin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:24381311 1315255 Dst dystonin gene MP:0001408 stereotypic behavior IEA N RGD:5509061 20150402 MGI 1315255 Dst dystonin gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:16087202 1315255 Dst dystonin gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1315255 Dst dystonin gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:16087202 1315255 Dst dystonin gene MP:0001504 abnormal posture IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:133598 1315255 Dst dystonin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:24381311 1315255 Dst dystonin gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:16087202 1315255 Dst dystonin gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:7736575 1315255 Dst dystonin gene MP:0001523 impaired righting response IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:133598 1315255 Dst dystonin gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:3138544 1315255 Dst dystonin gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20160304 MGI PMID:25195653 1315255 Dst dystonin gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16087202 1315255 Dst dystonin gene MP:0001527 athetotic walking movements IEA N RGD:5509061 20111116 MGI 1315255 Dst dystonin gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1315255 Dst dystonin gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:24381311 1315255 Dst dystonin gene MP:0002064 seizures IEA N RGD:5509061 20111116 MGI 1315255 Dst dystonin gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20111116 MGI 1315255 Dst dystonin gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:24381311 1315255 Dst dystonin gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:3138544 1315255 Dst dystonin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:133598 1315255 Dst dystonin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7736575 1315255 Dst dystonin gene MP:0002083 premature death IAGP N RGD:5509061 20160304 MGI PMID:25195653 1315255 Dst dystonin gene MP:0002083 premature death IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16087202 1315255 Dst dystonin gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:10357897 1315255 Dst dystonin gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:4655279 1315255 Dst dystonin gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:133598 1315255 Dst dystonin gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:4655279 1315255 Dst dystonin gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20160304 MGI PMID:25195653 1315255 Dst dystonin gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:7736575 1315255 Dst dystonin gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12859670 1315255 Dst dystonin gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:12859670 1315255 Dst dystonin gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10357897 1315255 Dst dystonin gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:7374955 1315255 Dst dystonin gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0002883 chromatolysis IEA N RGD:5509061 20111116 MGI 1315255 Dst dystonin gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:7736575 1315255 Dst dystonin gene MP:0002980 abnormal postural reflex IAGP N RGD:5509061 20141003 MGI PMID:16087202 1315255 Dst dystonin gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10357897 1315255 Dst dystonin gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:24381311 1315255 Dst dystonin gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20141003 MGI PMID:1634998 1315255 Dst dystonin gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20141003 MGI PMID:4655279 1315255 Dst dystonin gene MP:0003280 urinary incontinence IEA N RGD:5509061 20111116 MGI 1315255 Dst dystonin gene MP:0003281 fecal incontinence IEA N RGD:5509061 20111116 MGI 1315255 Dst dystonin gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141218 MGI PMID:4655279 1315255 Dst dystonin gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12859670 1315255 Dst dystonin gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:9570777 1315255 Dst dystonin gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:7736575 1315255 Dst dystonin gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:9570777 1315255 Dst dystonin gene MP:0003994 abnormal dorsal spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:3138544 1315255 Dst dystonin gene MP:0003994 abnormal dorsal spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:9581287 1315255 Dst dystonin gene MP:0003994 abnormal dorsal spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:9618216 1315255 Dst dystonin gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:24381311 1315255 Dst dystonin gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:10357897 1315255 Dst dystonin gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20160304 MGI PMID:25195653 1315255 Dst dystonin gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:12859670 1315255 Dst dystonin gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20160304 MGI PMID:25195653 1315255 Dst dystonin gene MP:0005150 cachexia IEA N RGD:5509061 20111116 MGI 1315255 Dst dystonin gene MP:0005191 head tilt IEA N RGD:5509061 20150402 MGI 1315255 Dst dystonin gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0005316 abnormal response to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:16087202 1315255 Dst dystonin gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:133598 1315255 Dst dystonin gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:7736575 1315255 Dst dystonin gene MP:0005323 dystonia IAGP N RGD:5509061 20160304 MGI PMID:25195653 1315255 Dst dystonin gene MP:0005323 dystonia IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0005356 positive geotaxis IAGP N RGD:5509061 20141003 MGI PMID:16087202 1315255 Dst dystonin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:12859670 1315255 Dst dystonin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:24381311 1315255 Dst dystonin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:9570777 1315255 Dst dystonin gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:12859670 1315255 Dst dystonin gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:24381311 1315255 Dst dystonin gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:7736575 1315255 Dst dystonin gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:9618216 1315255 Dst dystonin gene MP:0005405 axon degeneration IAGP N RGD:5509061 20160304 MGI PMID:25195653 1315255 Dst dystonin gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:16087202 1315255 Dst dystonin gene MP:0006198 enophthalmos IAGP N RGD:5509061 20141003 MGI PMID:16087202 1315255 Dst dystonin gene MP:0006258 abnormal circumvallate papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:16289886 1315255 Dst dystonin gene MP:0006260 abnormal gustatory papilla taste bud morphology IAGP N RGD:5509061 20230601 MGI PMID:16289886 1315255 Dst dystonin gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:24381311 1315255 Dst dystonin gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0009400 decreased skeletal muscle fiber size IEA N RGD:5509061 20111116 MGI 1315255 Dst dystonin gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1315255 Dst dystonin gene MP:0011085 postnatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1315255 Dst dystonin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1315255 Dst dystonin gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20160304 MGI PMID:25195653 1315255 Dst dystonin gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20180628 MGI PMID:27693510 1315255 Dst dystonin gene MP:0014344 abnormal skeletal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:10357897 1315260 Mtmr1 myotubularin related protein 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1315260 Mtmr1 myotubularin related protein 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1315260 Mtmr1 myotubularin related protein 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1315260 Mtmr1 myotubularin related protein 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0001147 small testis IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:21479251 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:21479251 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0006428 ectopic Sertoli cells IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:21479251 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0020356 abnormal Sertoli cell barrier function IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315262 Kpna6 karyopherin subunit alpha 6 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220721 MGI PMID:34473250 1315265 Anapc4 anaphase promoting complex subunit 4 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20240829 MGI PMID:38932933 1315265 Anapc4 anaphase promoting complex subunit 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315265 Anapc4 anaphase promoting complex subunit 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1315265 Anapc4 anaphase promoting complex subunit 4 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1315267 Exosc2 exosome component 2 gene MP:0001714 absent trophoblast giant cells IAGP N RGD:5509061 20240104 MGI PMID:37940010 1315267 Exosc2 exosome component 2 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20240104 MGI PMID:37940010 1315267 Exosc2 exosome component 2 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20240104 MGI PMID:37940010 1315267 Exosc2 exosome component 2 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20240104 MGI PMID:37940010 1315267 Exosc2 exosome component 2 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20240104 MGI PMID:37940010 1315267 Exosc2 exosome component 2 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20240104 MGI PMID:37940010 1315267 Exosc2 exosome component 2 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20240104 MGI PMID:37940010 1315267 Exosc2 exosome component 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315267 Exosc2 exosome component 2 gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20240104 MGI PMID:37940010 1315267 Exosc2 exosome component 2 gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20240104 MGI PMID:37940010 1315267 Exosc2 exosome component 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1315267 Exosc2 exosome component 2 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20240926 MGI PMID:37940010 1315269 Rfx1 regulatory factor X, 1 (influences HLA class II expression) gene MP:0001967 deafness IAGP N RGD:5509061 20170907 MGI PMID:26469318 1315269 Rfx1 regulatory factor X, 1 (influences HLA class II expression) gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20170907 MGI PMID:26469318 1315269 Rfx1 regulatory factor X, 1 (influences HLA class II expression) gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20170907 MGI PMID:26469318 1315269 Rfx1 regulatory factor X, 1 (influences HLA class II expression) gene MP:0004403 absent cochlear outer hair cells IAGP N RGD:5509061 20170907 MGI PMID:26469318 1315269 Rfx1 regulatory factor X, 1 (influences HLA class II expression) gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20170907 MGI PMID:26469318 1315269 Rfx1 regulatory factor X, 1 (influences HLA class II expression) gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20170907 MGI PMID:26469318 1315269 Rfx1 regulatory factor X, 1 (influences HLA class II expression) gene MP:0006325 impaired hearing IAGP N RGD:5509061 20170907 MGI PMID:26469318 1315269 Rfx1 regulatory factor X, 1 (influences HLA class II expression) gene MP:0011061 abnormal inner hair cell kinocilium morphology IAGP N RGD:5509061 20170907 MGI PMID:26469318 1315269 Rfx1 regulatory factor X, 1 (influences HLA class II expression) gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19559676 1315271 Lrpprc leucine-rich PPR-motif containing gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:22045337 1315271 Lrpprc leucine-rich PPR-motif containing gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22045337 1315271 Lrpprc leucine-rich PPR-motif containing gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21880015 1315271 Lrpprc leucine-rich PPR-motif containing gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1315271 Lrpprc leucine-rich PPR-motif containing gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:22045337 1315271 Lrpprc leucine-rich PPR-motif containing gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:21880015 1315271 Lrpprc leucine-rich PPR-motif containing gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22045337 1315271 Lrpprc leucine-rich PPR-motif containing gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:22045337 1315271 Lrpprc leucine-rich PPR-motif containing gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20190711 MGI PMID:22045337 1315274 Faf2 Fas associated factor family member 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161110 MGI PMID:25970332 1315274 Faf2 Fas associated factor family member 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20201022 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20201022 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20210128 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0001726 abnormal allantois morphology IEA N RGD:5509061 20201022 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210128 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20161110 MGI PMID:25970332 1315274 Faf2 Fas associated factor family member 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20161110 MGI PMID:25970332 1315274 Faf2 Fas associated factor family member 2 gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20201022 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20161110 MGI PMID:25970332 1315274 Faf2 Fas associated factor family member 2 gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20230601 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210128 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20210128 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20201022 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20210128 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20210128 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20161110 MGI PMID:25970332 1315274 Faf2 Fas associated factor family member 2 gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20161110 MGI PMID:25970332 1315274 Faf2 Fas associated factor family member 2 gene MP:0003981 decreased circulating phospholipid level IAGP N RGD:5509061 20161110 MGI PMID:25970332 1315274 Faf2 Fas associated factor family member 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20161110 MGI PMID:25970332 1315274 Faf2 Fas associated factor family member 2 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20201022 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0010331 abnormal apolipoprotein level IAGP N RGD:5509061 20161110 MGI PMID:25970332 1315274 Faf2 Fas associated factor family member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315274 Faf2 Fas associated factor family member 2 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:25970332 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0003786 premature aging IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0005114 premature hair loss IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0008869 anovulation IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20170330 MGI PMID:25843235 1315281 Ntmt1 N-terminal Xaa-Pro-Lys N-methyltransferase 1 gene MP:0014273 abnormal skin vasculature morphology IAGP N RGD:5509061 20230810 MGI PMID:25843235 1315288 Pkdrej polycystin (PKD) family receptor for egg jelly gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1315288 Pkdrej polycystin (PKD) family receptor for egg jelly gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20141003 MGI PMID:18562295 1315292 Gca grancalcin gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12529388 1315294 Agfg2 ArfGAP with FG repeats 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1315296 Tmem184b transmembrane protein 184b gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1315296 Tmem184b transmembrane protein 184b gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1315296 Tmem184b transmembrane protein 184b gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20160811 MGI PMID:27122027 1315296 Tmem184b transmembrane protein 184b gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1315296 Tmem184b transmembrane protein 184b gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1315296 Tmem184b transmembrane protein 184b gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1315296 Tmem184b transmembrane protein 184b gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1315296 Tmem184b transmembrane protein 184b gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1315296 Tmem184b transmembrane protein 184b gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20160811 MGI PMID:27122027 1315296 Tmem184b transmembrane protein 184b gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1315296 Tmem184b transmembrane protein 184b gene MP:0002574 increased vertical activity IEA N RGD:5509061 20231207 MGI 1315296 Tmem184b transmembrane protein 184b gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20160811 MGI PMID:27122027 1315296 Tmem184b transmembrane protein 184b gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20160811 MGI PMID:27122027 1315296 Tmem184b transmembrane protein 184b gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20160811 MGI PMID:27122027 1315296 Tmem184b transmembrane protein 184b gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 1315296 Tmem184b transmembrane protein 184b gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20160811 MGI PMID:27122027 1315296 Tmem184b transmembrane protein 184b gene MP:0005405 axon degeneration IAGP N RGD:5509061 20160811 MGI PMID:27122027 1315296 Tmem184b transmembrane protein 184b gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20160811 MGI PMID:27122027 1315296 Tmem184b transmembrane protein 184b gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20160811 MGI PMID:27122027 1315296 Tmem184b transmembrane protein 184b gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160811 MGI PMID:27122027 1315296 Tmem184b transmembrane protein 184b gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1315296 Tmem184b transmembrane protein 184b gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1315302 Oscp1 organic solute carrier partner 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 1315302 Oscp1 organic solute carrier partner 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20211021 MGI 1315304 Cyc1 cytochrome c-1 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20241010 MGI 1315304 Cyc1 cytochrome c-1 gene MP:0003886 abnormal embryonic epiblast morphology IEA N RGD:5509061 20241010 MGI 1315304 Cyc1 cytochrome c-1 gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IEA N RGD:5509061 20241010 MGI 1315304 Cyc1 cytochrome c-1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241010 MGI 1315304 Cyc1 cytochrome c-1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1315304 Cyc1 cytochrome c-1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1315308 Urm1 ubiquitin related modifier 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1315308 Urm1 ubiquitin related modifier 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 1315308 Urm1 ubiquitin related modifier 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1315308 Urm1 ubiquitin related modifier 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1315315 Cyp46a1 cytochrome P450, family 46, subfamily a, polypeptide 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12686551 1315317 Eppin epididymal peptidase inhibitor gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210826 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230601 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0009476 enlarged cecum IEA N RGD:5509061 20210826 MGI 1315317 Eppin epididymal peptidase inhibitor gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1315319 Trip12 thyroid hormone receptor interactor 12 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20200310 MGI PMID:22028794 1315319 Trip12 thyroid hormone receptor interactor 12 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20200310 MGI PMID:22028794 1315319 Trip12 thyroid hormone receptor interactor 12 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:23747016 1315319 Trip12 thyroid hormone receptor interactor 12 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:22028794 1315319 Trip12 thyroid hormone receptor interactor 12 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20200310 MGI PMID:23747016 1315319 Trip12 thyroid hormone receptor interactor 12 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22028794 1315324 Otog otogelin gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0001394 circling IAGP N RGD:5509061 20170427 MGI PMID:26636018 1315324 Otog otogelin gene MP:0001394 circling IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315324 Otog otogelin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315324 Otog otogelin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315324 Otog otogelin gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20170427 MGI PMID:26636018 1315324 Otog otogelin gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315324 Otog otogelin gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0001522 impaired swimming IAGP N RGD:5509061 20170427 MGI PMID:26636018 1315324 Otog otogelin gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0001523 impaired righting response IAGP N RGD:5509061 20170427 MGI PMID:26636018 1315324 Otog otogelin gene MP:0001523 impaired righting response IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315324 Otog otogelin gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0001525 impaired balance IAGP N RGD:5509061 20170427 MGI PMID:26636018 1315324 Otog otogelin gene MP:0001525 impaired balance IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315324 Otog otogelin gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315324 Otog otogelin gene MP:0001921 reduced fertility IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315324 Otog otogelin gene MP:0001967 deafness IEA N RGD:5509061 20111116 MGI 1315324 Otog otogelin gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20240523 MGI 1315324 Otog otogelin gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0002894 abnormal otolith morphology IEA N RGD:5509061 20111116 MGI 1315324 Otog otogelin gene MP:0002895 abnormal otolithic membrane morphology IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315324 Otog otogelin gene MP:0003145 detached otolithic membrane IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0003145 detached otolithic membrane IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315324 Otog otogelin gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0003878 abnormal ear physiology IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315324 Otog otogelin gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20170427 MGI PMID:26636018 1315324 Otog otogelin gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315324 Otog otogelin gene MP:0004330 abnormal vestibular saccular macula morphology IAGP N RGD:5509061 20170427 MGI PMID:26636018 1315324 Otog otogelin gene MP:0004517 decreased vestibular hair cell stereocilia number IAGP N RGD:5509061 20170427 MGI PMID:26636018 1315324 Otog otogelin gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1315324 Otog otogelin gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0005191 head tilt IAGP N RGD:5509061 20170427 MGI PMID:26636018 1315324 Otog otogelin gene MP:0005191 head tilt IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315324 Otog otogelin gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0006325 impaired hearing IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315324 Otog otogelin gene MP:0006328 nonsyndromic hearing impairment IAGP N RGD:5509061 20170427 MGI PMID:26636018 1315324 Otog otogelin gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315324 Otog otogelin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1315324 Otog otogelin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:10655058 1315324 Otog otogelin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20220407 MGI PMID:11178734 1315328 Car12 carbonic anhydrase 12 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16800892 1315330 Yae1d1 Yae1 domain containing 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1315330 Yae1d1 Yae1 domain containing 1 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1315330 Yae1d1 Yae1 domain containing 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1315330 Yae1d1 Yae1 domain containing 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1315330 Yae1d1 Yae1 domain containing 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1315330 Yae1d1 Yae1 domain containing 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1315330 Yae1d1 Yae1 domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315330 Yae1d1 Yae1 domain containing 1 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 1315335 Mcm5 minichromosome maintenance complex component 5 gene MP:0008762 embryonic lethality IEA N RGD:5509061 20141003 MGI 1315337 Sptlc1 serine palmitoyltransferase, long chain base subunit 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:16216550 1315337 Sptlc1 serine palmitoyltransferase, long chain base subunit 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1315337 Sptlc1 serine palmitoyltransferase, long chain base subunit 1 gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:16216550 1315337 Sptlc1 serine palmitoyltransferase, long chain base subunit 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1315337 Sptlc1 serine palmitoyltransferase, long chain base subunit 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16216550 1315337 Sptlc1 serine palmitoyltransferase, long chain base subunit 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315339 Prnd prion like protein doppel gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:15161660 1315339 Prnd prion like protein doppel gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12110578 1315339 Prnd prion like protein doppel gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15007175 1315339 Prnd prion like protein doppel gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15161660 1315339 Prnd prion like protein doppel gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12110578 1315339 Prnd prion like protein doppel gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12110578 1315339 Prnd prion like protein doppel gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12110578 1315339 Prnd prion like protein doppel gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:15161660 1315339 Prnd prion like protein doppel gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12110578 1315339 Prnd prion like protein doppel gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15007175 1315339 Prnd prion like protein doppel gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:12110578 1315339 Prnd prion like protein doppel gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:12110578 1315339 Prnd prion like protein doppel gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:12110578 1315339 Prnd prion like protein doppel gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20191017 MGI PMID:12110578 1315341 Cbx5 chromobox 5 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1315341 Cbx5 chromobox 5 gene MP:0003036 vertebral transformation IEA N RGD:5509061 20141003 MGI 1315341 Cbx5 chromobox 5 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20150430 MGI 1315341 Cbx5 chromobox 5 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20150430 MGI 1315341 Cbx5 chromobox 5 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:22763435 1315341 Cbx5 chromobox 5 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20201022 MGI 1315341 Cbx5 chromobox 5 gene MP:0008762 embryonic lethality IEA N RGD:5509061 20141003 MGI 1315341 Cbx5 chromobox 5 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1315341 Cbx5 chromobox 5 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22670227 1315343 Map2k3 mitogen-activated protein kinase kinase 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17723219 1315343 Map2k3 mitogen-activated protein kinase kinase 3 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12151339 1315343 Map2k3 mitogen-activated protein kinase kinase 3 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12151339 1315343 Map2k3 mitogen-activated protein kinase kinase 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17723219 1315347 Carmil1 capping protein regulator and myosin 1 linker 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160915 MGI PMID:24652767 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20180607 MGI PMID:28433741 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180607 MGI PMID:28433741 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20180607 MGI PMID:28433741 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20180607 MGI PMID:28433741 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180607 MGI PMID:28433741 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20180607 MGI PMID:28433741 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0001440 abnormal grooming behavior IAGP N RGD:5509061 20180607 MGI PMID:28433741 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20180607 MGI PMID:28433741 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0005655 increased aggression IEA N RGD:5509061 20220811 MGI 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20180607 MGI PMID:28433741 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180607 MGI PMID:28433741 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20180607 MGI PMID:28433741 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0013894 abnormal behavioral response to amphetamine IAGP N RGD:5509061 20180607 MGI PMID:28433741 1315348 Zswim6 zinc finger SWIM-type containing 6 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:28433741 1315349 Smim23 small integral membrane protein 23 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20201022 MGI 1315349 Smim23 small integral membrane protein 23 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1315349 Smim23 small integral membrane protein 23 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20201022 MGI 1315350 Tmbim7 transmembrane BAX inhibitor motif containing 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20161222 MGI PMID:26216965 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0000120 malocclusion IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20161222 MGI PMID:26216965 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0001261 obese IAGP N RGD:5509061 20161222 MGI PMID:26216965 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0001261 obese IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20211209 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20211209 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20211209 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20211209 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20211209 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20211209 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20161222 MGI PMID:26216965 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20211209 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20211209 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20161222 MGI PMID:26216965 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20161222 MGI PMID:26216965 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20161222 MGI PMID:26216965 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20161222 MGI PMID:26216965 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20161222 MGI PMID:26216965 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20161222 MGI PMID:26216965 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20211209 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20211209 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20211209 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20211209 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0009500 abnormal interlobular bile duct morphology IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20211209 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0009837 abnormal sperm end piece morphology IAGP N RGD:5509061 20220217 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20161222 MGI PMID:26216965 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20161222 MGI PMID:26216965 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20211209 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0011998 decreased embryonic cilium length IAGP N RGD:5509061 20230302 MGI PMID:30423168 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20161222 MGI PMID:26216965 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20161222 MGI PMID:26216965 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20211209 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0031351 abnormal sperm flagellum thickness IAGP N RGD:5509061 20220317 MGI PMID:34023333 1315353 Lztfl1 leucine zipper transcription factor-like 1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:26216965 1315354 Anapc1 anaphase promoting complex subunit 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1315354 Anapc1 anaphase promoting complex subunit 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1315354 Anapc1 anaphase promoting complex subunit 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1315354 Anapc1 anaphase promoting complex subunit 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315354 Anapc1 anaphase promoting complex subunit 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1315358 Deup1 deuterosome assembly protein 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20231207 MGI 1315358 Deup1 deuterosome assembly protein 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20231207 MGI 1315358 Deup1 deuterosome assembly protein 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20210520 MGI 1315358 Deup1 deuterosome assembly protein 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20231207 MGI 1315358 Deup1 deuterosome assembly protein 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20231207 MGI 1315358 Deup1 deuterosome assembly protein 1 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 1315361 Maz MYC-associated zinc finger protein (purine-binding transcription factor) gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20200514 MGI 1315361 Maz MYC-associated zinc finger protein (purine-binding transcription factor) gene MP:0000520 absent kidney IAGP N RGD:5509061 20180920 MGI PMID:29432158 1315361 Maz MYC-associated zinc finger protein (purine-binding transcription factor) gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1315361 Maz MYC-associated zinc finger protein (purine-binding transcription factor) gene MP:0001925 male infertility IAGP N RGD:5509061 20180920 MGI PMID:29432158 1315361 Maz MYC-associated zinc finger protein (purine-binding transcription factor) gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20180920 MGI PMID:29432158 1315361 Maz MYC-associated zinc finger protein (purine-binding transcription factor) gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20180920 MGI PMID:29432158 1315361 Maz MYC-associated zinc finger protein (purine-binding transcription factor) gene MP:0003604 single kidney IAGP N RGD:5509061 20180920 MGI PMID:29432158 1315361 Maz MYC-associated zinc finger protein (purine-binding transcription factor) gene MP:0003617 urinary bladder hypoplasia IAGP N RGD:5509061 20180920 MGI PMID:29432158 1315361 Maz MYC-associated zinc finger protein (purine-binding transcription factor) gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20180920 MGI PMID:29432158 1315361 Maz MYC-associated zinc finger protein (purine-binding transcription factor) gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1315361 Maz MYC-associated zinc finger protein (purine-binding transcription factor) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180920 MGI PMID:29432158 1315361 Maz MYC-associated zinc finger protein (purine-binding transcription factor) gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20180920 MGI PMID:29432158 1315361 Maz MYC-associated zinc finger protein (purine-binding transcription factor) gene MP:0011923 abnormal bladder urine volume IAGP N RGD:5509061 20180920 MGI PMID:29432158 1315362 Mrfap1 Morf4 family associated protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15367658 1315363 Asphd1 aspartate beta-hydroxylase domain containing 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1315363 Asphd1 aspartate beta-hydroxylase domain containing 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1315363 Asphd1 aspartate beta-hydroxylase domain containing 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1315363 Asphd1 aspartate beta-hydroxylase domain containing 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1315363 Asphd1 aspartate beta-hydroxylase domain containing 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230601 MGI 1315363 Asphd1 aspartate beta-hydroxylase domain containing 1 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230601 MGI 1315363 Asphd1 aspartate beta-hydroxylase domain containing 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20230601 MGI 1315363 Asphd1 aspartate beta-hydroxylase domain containing 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1315363 Asphd1 aspartate beta-hydroxylase domain containing 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20230601 MGI 1315363 Asphd1 aspartate beta-hydroxylase domain containing 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230601 MGI 1315365 Atxn2 ataxin 2 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16293225 1315365 Atxn2 ataxin 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22956915 1315365 Atxn2 ataxin 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16293225 1315365 Atxn2 ataxin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22956915 1315365 Atxn2 ataxin 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:18250099 1315365 Atxn2 ataxin 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16293225 1315365 Atxn2 ataxin 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22956915 1315365 Atxn2 ataxin 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:18250099 1315365 Atxn2 ataxin 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:18250099 1315365 Atxn2 ataxin 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18250099 1315365 Atxn2 ataxin 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18250099 1315365 Atxn2 ataxin 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16293225 1315365 Atxn2 ataxin 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:18250099 1315365 Atxn2 ataxin 2 gene MP:0002997 enlarged seminal vesicle IAGP N RGD:5509061 20141204 MGI PMID:16293225 1315365 Atxn2 ataxin 2 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:18250099 1315365 Atxn2 ataxin 2 gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:18250099 1315365 Atxn2 ataxin 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18250099 1315365 Atxn2 ataxin 2 gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20141003 MGI PMID:16293225 1315365 Atxn2 ataxin 2 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:18250099 1315365 Atxn2 ataxin 2 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18250099 1315365 Atxn2 ataxin 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18250099 1315365 Atxn2 ataxin 2 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18250099 1315365 Atxn2 ataxin 2 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:18250099 1315365 Atxn2 ataxin 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18250099 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:10481911 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:10862711 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:10481911 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:10862711 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20220519 MGI PMID:28797108 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20220519 MGI PMID:28797108 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:10481911 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10481911 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10862711 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:10862711 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20220519 MGI PMID:28797108 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:10481911 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20171109 MGI PMID:23695275 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0002833 increased heart weight IAGP N RGD:5509061 20171109 MGI PMID:23695275 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:10481911 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0003024 coronary artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:10481911 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20171109 MGI PMID:23695275 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10481911 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20171109 MGI PMID:23695275 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20220519 MGI PMID:28797108 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:10481911 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20171109 MGI PMID:23695275 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:10481911 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:10862711 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20220519 MGI PMID:28797108 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10862711 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:10481911 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20231221 MGI PMID:10481911 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0009416 cardiac muscle degeneration IAGP N RGD:5509061 20171109 MGI PMID:23695275 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20220519 MGI PMID:28797108 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10481911 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20220519 MGI PMID:28797108 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:10862711 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20220519 MGI PMID:28797108 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0010394 decreased QRS amplitude IAGP N RGD:5509061 20141003 MGI PMID:10481911 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20171109 MGI PMID:23695275 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20171109 MGI PMID:23695275 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0011749 perivascular fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10862711 1315367 Sgcd sarcoglycan, delta (dystrophin-associated glycoprotein) gene MP:0012735 abnormal response to exercise IAGP N RGD:5509061 20171109 MGI PMID:23695275 1315372 Tenm3 teneurin transmembrane protein 3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17803360 1315372 Tenm3 teneurin transmembrane protein 3 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:17803360 1315372 Tenm3 teneurin transmembrane protein 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17803360 1315375 Fam120a family with sequence similarity 120, member A gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20211021 MGI 1315375 Fam120a family with sequence similarity 120, member A gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1315375 Fam120a family with sequence similarity 120, member A gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1315375 Fam120a family with sequence similarity 120, member A gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20240523 MGI 1315375 Fam120a family with sequence similarity 120, member A gene MP:0002833 increased heart weight IEA N RGD:5509061 20220519 MGI 1315375 Fam120a family with sequence similarity 120, member A gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1315375 Fam120a family with sequence similarity 120, member A gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1315375 Fam120a family with sequence similarity 120, member A gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1315375 Fam120a family with sequence similarity 120, member A gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1315375 Fam120a family with sequence similarity 120, member A gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21741597 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:18787701 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21741597 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18787701 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:18787701 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21741597 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21741597 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18787701 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20190411 MGI PMID:28627522 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21741597 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21159644 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21741597 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21741597 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20190411 MGI PMID:28627522 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18787701 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21741597 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20190411 MGI PMID:28627522 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18787701 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:18787701 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21741597 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21741597 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21741597 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18787701 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20190411 MGI PMID:28627522 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21741597 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21741597 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0010559 heart block IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18285465 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18787701 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21159644 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0011394 increased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21289070 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20160428 MGI PMID:18787701 1315377 Dot1l DOT1 like histone lysine methyltransferase gene MP:0030928 increased telomere length IAGP N RGD:5509061 20190117 MGI PMID:18787701 1315378 Znrf1 zinc and ring finger 1 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20191114 MGI PMID:28593998 1315378 Znrf1 zinc and ring finger 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20191114 MGI PMID:28593998 1315383 Spryd4 SPRY domain containing 4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1315383 Spryd4 SPRY domain containing 4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20201022 MGI 1315383 Spryd4 SPRY domain containing 4 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20201022 MGI 1315383 Spryd4 SPRY domain containing 4 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20201022 MGI 1315383 Spryd4 SPRY domain containing 4 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220519 MGI 1315385 Lamc2 laminin, gamma 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20170209 MGI PMID:14632187 1315385 Lamc2 laminin, gamma 2 gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20170209 MGI PMID:14632187 1315385 Lamc2 laminin, gamma 2 gene MP:0000578 ulcerated autopod IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0000578 ulcerated autopod IAGP N RGD:5509061 20240822 MGI PMID:37796769 1315385 Lamc2 laminin, gamma 2 gene MP:0001190 reddish skin IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0001208 blistering IAGP N RGD:5509061 20170209 MGI PMID:14632187 1315385 Lamc2 laminin, gamma 2 gene MP:0001208 blistering IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0001208 blistering IAGP N RGD:5509061 20240822 MGI PMID:37796769 1315385 Lamc2 laminin, gamma 2 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0001438 aphagia IAGP N RGD:5509061 20170209 MGI PMID:14632187 1315385 Lamc2 laminin, gamma 2 gene MP:0001849 ear inflammation IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0001849 ear inflammation IAGP N RGD:5509061 20240822 MGI PMID:37796769 1315385 Lamc2 laminin, gamma 2 gene MP:0001874 acanthosis IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20170209 MGI PMID:14632187 1315385 Lamc2 laminin, gamma 2 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20240822 MGI PMID:37796769 1315385 Lamc2 laminin, gamma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20240829 MGI PMID:37796769 1315385 Lamc2 laminin, gamma 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20170209 MGI PMID:14632187 1315385 Lamc2 laminin, gamma 2 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20170209 MGI PMID:22507638 1315385 Lamc2 laminin, gamma 2 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20240822 MGI PMID:37796769 1315385 Lamc2 laminin, gamma 2 gene MP:0004273 abnormal basal lamina morphology IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0005275 abnormal skin tensile strength IAGP N RGD:5509061 20240822 MGI PMID:37796769 1315385 Lamc2 laminin, gamma 2 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0009827 skin detachment IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0009827 skin detachment IAGP N RGD:5509061 20240822 MGI PMID:37796769 1315385 Lamc2 laminin, gamma 2 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0010936 decreased airway resistance IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0011045 decreased lung elastance IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:14632187 1315385 Lamc2 laminin, gamma 2 gene MP:0011159 abnormal epidermal-dermal junction morphology IAGP N RGD:5509061 20170209 MGI PMID:22507638 1315385 Lamc2 laminin, gamma 2 gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20170209 MGI PMID:14632187 1315385 Lamc2 laminin, gamma 2 gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20170209 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20170209 MGI PMID:22507638 1315385 Lamc2 laminin, gamma 2 gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20240822 MGI PMID:37796769 1315385 Lamc2 laminin, gamma 2 gene MP:0012400 nail dystrophy IAGP N RGD:5509061 20240822 MGI PMID:37796769 1315385 Lamc2 laminin, gamma 2 gene MP:0012402 abnormal nail bed morphology IAGP N RGD:5509061 20240822 MGI PMID:37796769 1315385 Lamc2 laminin, gamma 2 gene MP:0030423 abnormal pinna cartilage morphology IAGP N RGD:5509061 20171214 MGI PMID:20336083 1315385 Lamc2 laminin, gamma 2 gene MP:0030460 enamel pits IAGP N RGD:5509061 20171221 MGI PMID:20336083 1315388 Prss16 serine protease 16 (thymus) gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19283781 1315388 Prss16 serine protease 16 (thymus) gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19283781 1315388 Prss16 serine protease 16 (thymus) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15632078 1315388 Prss16 serine protease 16 (thymus) gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19283781 1315388 Prss16 serine protease 16 (thymus) gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:19283781 1315388 Prss16 serine protease 16 (thymus) gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19283781 1315388 Prss16 serine protease 16 (thymus) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19283781 1315388 Prss16 serine protease 16 (thymus) gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19283781 1315388 Prss16 serine protease 16 (thymus) gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19283781 1315388 Prss16 serine protease 16 (thymus) gene MP:0008195 abnormal professional antigen presenting cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19283781 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12551952 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:16476774 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:16476774 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16476774 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:16476774 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:16476774 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:10995385 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:10995385 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:16476774 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:12551952 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:16476774 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:12551952 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:16476774 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:12551952 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:16476774 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:12551952 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:10995385 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:16476774 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0008007 abnormal cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:16476774 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16476774 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16476774 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10995385 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12551952 1315391 Bub3 BUB3 mitotic checkpoint protein gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:16476774 1315393 Arvcf armadillo repeat gene deleted in velocardiofacial syndrome gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20170105 MGI 1315393 Arvcf armadillo repeat gene deleted in velocardiofacial syndrome gene MP:0001304 cataract IEA N RGD:5509061 20141003 MGI 1315393 Arvcf armadillo repeat gene deleted in velocardiofacial syndrome gene MP:0001399 hyperactivity IEA N RGD:5509061 20160804 MGI 1315393 Arvcf armadillo repeat gene deleted in velocardiofacial syndrome gene MP:0001406 abnormal gait IEA N RGD:5509061 20141003 MGI 1315393 Arvcf armadillo repeat gene deleted in velocardiofacial syndrome gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1315393 Arvcf armadillo repeat gene deleted in velocardiofacial syndrome gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1315394 Inca1 inhibitor of CDK, cyclin A1 interacting protein 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21540187 1315394 Inca1 inhibitor of CDK, cyclin A1 interacting protein 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:21540187 1315394 Inca1 inhibitor of CDK, cyclin A1 interacting protein 1 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:21540187 1315394 Inca1 inhibitor of CDK, cyclin A1 interacting protein 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:21540187 1315394 Inca1 inhibitor of CDK, cyclin A1 interacting protein 1 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21540187 1315394 Inca1 inhibitor of CDK, cyclin A1 interacting protein 1 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:21540187 1315394 Inca1 inhibitor of CDK, cyclin A1 interacting protein 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:21540187 1315396 Usp32 ubiquitin specific peptidase 32 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1315396 Usp32 ubiquitin specific peptidase 32 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20230601 MGI 1315396 Usp32 ubiquitin specific peptidase 32 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1315396 Usp32 ubiquitin specific peptidase 32 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230601 MGI 1315396 Usp32 ubiquitin specific peptidase 32 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20230601 MGI 1315396 Usp32 ubiquitin specific peptidase 32 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 1315396 Usp32 ubiquitin specific peptidase 32 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20230601 MGI 1315396 Usp32 ubiquitin specific peptidase 32 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230601 MGI 1315396 Usp32 ubiquitin specific peptidase 32 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230601 MGI 1315396 Usp32 ubiquitin specific peptidase 32 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230601 MGI 1315396 Usp32 ubiquitin specific peptidase 32 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000098 abnormal vomer bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:18606991 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:10898787 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10898787 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:10898787 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10898787 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230119 MGI 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001147 small testis IEA N RGD:5509061 20230119 MGI 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001230 epidermal desquamation IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001241 absent epidermis stratum corneum IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001241 absent epidermis stratum corneum IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001297 microphthalmia IEA N RGD:5509061 20230119 MGI 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:11053261 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001310 abnormal conjunctiva morphology IAGP N RGD:5509061 20141003 MGI PMID:11053261 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:11053261 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18606991 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:11747812 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18606991 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230119 MGI 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20231207 MGI 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230119 MGI 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16973390 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002544 brachydactyly IAGP N RGD:5509061 20231130 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18606991 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18606991 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:16973390 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:10898787 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:10898787 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0003142 anotia IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0003276 esophageal atresia IAGP N RGD:5509061 20150319 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20231695 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10898787 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:22366192 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004379 wide frontal bone IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004418 small parietal bone IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004546 esophagus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004574 broad limb buds IAGP N RGD:5509061 20141003 MGI PMID:10898787 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004622 sacral vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004657 small sacral vertebrae IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20150319 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:16973390 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004838 abnormal neural fold elevation formation IAGP N RGD:5509061 20141003 MGI PMID:10898787 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004882 enlarged lung IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:18606991 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:11053261 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:11053261 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:18606991 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:14960276 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:22366192 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20141003 MGI PMID:18606991 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10898787 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:11747812 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16973390 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:16973390 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:16973390 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:16973390 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008717 increased lung squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:20231695 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20231695 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:18606991 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18606991 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0008991 abnormal bile canaliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:18606991 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0009343 dilated gallbladder IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11747812 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:11747812 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0009560 absent epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0009560 absent epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20150319 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0009709 hydrometra IEA N RGD:5509061 20230119 MGI 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20170309 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:14960276 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0010799 stomach mucosa hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23597566 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0010864 abnormal enamel knot morphology IAGP N RGD:5509061 20171221 MGI PMID:14960276 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0010880 small esophagus IAGP N RGD:5509061 20150319 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18772111 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10195895 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17351639 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10898787 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10898787 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0011706 abnormal fibroblast migration IAGP N RGD:5509061 20141003 MGI PMID:20231695 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20170223 MGI PMID:20231695 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10898787 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0012279 wide sternum IAGP N RGD:5509061 20141003 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10898787 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0013129 abnormal tooth color IEA N RGD:5509061 20230119 MGI 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0013182 increased spinal cord apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10898787 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0020416 decreased fibroblast chemotaxis IAGP N RGD:5509061 20170223 MGI PMID:20231695 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0020859 disorganized cornea epithelium IAGP N RGD:5509061 20181101 MGI PMID:11053261 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0030079 small incisors IAGP N RGD:5509061 20170928 MGI PMID:10346820 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0030197 small nasal septum IAGP N RGD:5509061 20171012 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0030266 small vomer bone IAGP N RGD:5509061 20171026 MGI PMID:10195896 1315402 Chuk conserved helix-loop-helix ubiquitous kinase gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20171221 MGI PMID:14960276 1315407 Fbxo22 F-box protein 22 gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20210128 MGI 1315407 Fbxo22 F-box protein 22 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1315407 Fbxo22 F-box protein 22 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1315407 Fbxo22 F-box protein 22 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20181227 MGI 1315407 Fbxo22 F-box protein 22 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20230831 MGI PMID:26868148 1315407 Fbxo22 F-box protein 22 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1315407 Fbxo22 F-box protein 22 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1315407 Fbxo22 F-box protein 22 gene MP:0010580 decreased heart left ventricle size IEA N RGD:5509061 20210128 MGI 1315407 Fbxo22 F-box protein 22 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20230831 MGI PMID:26868148 1315407 Fbxo22 F-box protein 22 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20230831 MGI PMID:26868148 1315411 Ppp2r5d protein phosphatase 2, regulatory subunit B', delta gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21482799 1315411 Ppp2r5d protein phosphatase 2, regulatory subunit B', delta gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20592205 1315411 Ppp2r5d protein phosphatase 2, regulatory subunit B', delta gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21482799 1315411 Ppp2r5d protein phosphatase 2, regulatory subunit B', delta gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:21482799 1315411 Ppp2r5d protein phosphatase 2, regulatory subunit B', delta gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:20592205 1315412 Prss34 serine protease 34 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20211202 MGI PMID:27789480 1315412 Prss34 serine protease 34 gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20211202 MGI PMID:27789480 1315414 Fis1 fission, mitochondrial 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20200806 MGI PMID:31526891 1315414 Fis1 fission, mitochondrial 1 gene MP:0001147 small testis IAGP N RGD:5509061 20210916 MGI PMID:34355730 1315414 Fis1 fission, mitochondrial 1 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20200806 MGI PMID:31526891 1315414 Fis1 fission, mitochondrial 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210916 MGI PMID:34355730 1315414 Fis1 fission, mitochondrial 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20210916 MGI PMID:34355730 1315414 Fis1 fission, mitochondrial 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20210128 MGI 1315414 Fis1 fission, mitochondrial 1 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20200806 MGI PMID:31526891 1315414 Fis1 fission, mitochondrial 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20200806 MGI PMID:31526891 1315414 Fis1 fission, mitochondrial 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210916 MGI PMID:34355730 1315414 Fis1 fission, mitochondrial 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20200806 MGI PMID:31526891 1315414 Fis1 fission, mitochondrial 1 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20200806 MGI PMID:31526891 1315414 Fis1 fission, mitochondrial 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20200806 MGI PMID:31526891 1315414 Fis1 fission, mitochondrial 1 gene MP:0008608 increased circulating interleukin-13 level IAGP N RGD:5509061 20200806 MGI PMID:31526891 1315414 Fis1 fission, mitochondrial 1 gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20200806 MGI PMID:31526891 1315414 Fis1 fission, mitochondrial 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315414 Fis1 fission, mitochondrial 1 gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20210916 MGI PMID:34355730 1315414 Fis1 fission, mitochondrial 1 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20200806 MGI PMID:31526891 1315414 Fis1 fission, mitochondrial 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20200806 MGI PMID:31526891 1315414 Fis1 fission, mitochondrial 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20200806 MGI PMID:31526891 1315414 Fis1 fission, mitochondrial 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20210916 MGI PMID:34355730 1315414 Fis1 fission, mitochondrial 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20210916 MGI PMID:34355730 1315414 Fis1 fission, mitochondrial 1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20210916 MGI PMID:34355730 1315416 Arhgap24 Rho GTPase activating protein 24 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20201022 MGI 1315416 Arhgap24 Rho GTPase activating protein 24 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20210128 MGI 1315416 Arhgap24 Rho GTPase activating protein 24 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20200402 MGI 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:12947200 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:12947200 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12947200 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12947200 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20190919 MGI PMID:28196692 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0004806 absent germ cells IAGP N RGD:5509061 20141003 MGI PMID:12947200 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12947200 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20190919 MGI PMID:28196692 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:12947200 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20240530 MGI PMID:38325858 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:18281459 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0006361 abnormal female germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18281459 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20190919 MGI PMID:28196692 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20240530 MGI PMID:38325858 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12947200 1315422 Nanos3 nanos C2HC-type zinc finger 3 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20190418 MGI PMID:27353389 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0001023 L5 dorsal root ganglion hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315430 Dock3 dedicator of cyto-kinesis 3 gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20141003 MGI PMID:19129390 1315432 Brdt bromodomain, testis-specific gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20160915 MGI PMID:26994494 1315432 Brdt bromodomain, testis-specific gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17728347 1315432 Brdt bromodomain, testis-specific gene MP:0001925 male infertility IAGP N RGD:5509061 20160915 MGI PMID:26994494 1315432 Brdt bromodomain, testis-specific gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20160915 MGI PMID:26994494 1315432 Brdt bromodomain, testis-specific gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20160915 MGI PMID:26994494 1315432 Brdt bromodomain, testis-specific gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220714 MGI PMID:17728347 1315432 Brdt bromodomain, testis-specific gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220714 MGI PMID:17728347 1315432 Brdt bromodomain, testis-specific gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20160915 MGI PMID:26994494 1315432 Brdt bromodomain, testis-specific gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20141003 MGI 1315432 Brdt bromodomain, testis-specific gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20160915 MGI PMID:26994494 1315432 Brdt bromodomain, testis-specific gene MP:0005159 azoospermia IAGP N RGD:5509061 20160915 MGI PMID:26994494 1315432 Brdt bromodomain, testis-specific gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220714 MGI PMID:17728347 1315432 Brdt bromodomain, testis-specific gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20160915 MGI PMID:26994494 1315432 Brdt bromodomain, testis-specific gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17728347 1315432 Brdt bromodomain, testis-specific gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20160915 MGI PMID:26994494 1315432 Brdt bromodomain, testis-specific gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:22922464 1315432 Brdt bromodomain, testis-specific gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20160915 MGI PMID:26994494 1315432 Brdt bromodomain, testis-specific gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220714 MGI PMID:17728347 1315432 Brdt bromodomain, testis-specific gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220714 MGI PMID:17728347 1315432 Brdt bromodomain, testis-specific gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220714 MGI PMID:17728347 1315432 Brdt bromodomain, testis-specific gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20141003 MGI 1315432 Brdt bromodomain, testis-specific gene MP:0013330 abnormal male accessory sex gland morphology IAGP N RGD:5509061 20160915 MGI PMID:26994494 1315432 Brdt bromodomain, testis-specific gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20160915 MGI PMID:26994494 1315432 Brdt bromodomain, testis-specific gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220714 MGI PMID:17728347 1315437 Smoc2 SPARC related modular calcium binding 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1315437 Smoc2 SPARC related modular calcium binding 2 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20180426 MGI PMID:28552356 1315437 Smoc2 SPARC related modular calcium binding 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20201022 MGI 1315437 Smoc2 SPARC related modular calcium binding 2 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 1315437 Smoc2 SPARC related modular calcium binding 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20221215 MGI 1315437 Smoc2 SPARC related modular calcium binding 2 gene MP:0003760 decreased palatal length IAGP N RGD:5509061 20180426 MGI PMID:28552356 1315437 Smoc2 SPARC related modular calcium binding 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201022 MGI 1315437 Smoc2 SPARC related modular calcium binding 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180308 MGI PMID:28422762 1315437 Smoc2 SPARC related modular calcium binding 2 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20221215 MGI 1315437 Smoc2 SPARC related modular calcium binding 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1315437 Smoc2 SPARC related modular calcium binding 2 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20180426 MGI PMID:28552356 1315442 Spaca3 sperm acrosome associated 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1315445 Mrpl51 mitochondrial ribosomal protein L51 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1315445 Mrpl51 mitochondrial ribosomal protein L51 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315445 Mrpl51 mitochondrial ribosomal protein L51 gene MP:0011435 increased urine magnesium level IEA N RGD:5509061 20210128 MGI 1315445 Mrpl51 mitochondrial ribosomal protein L51 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1315445 Mrpl51 mitochondrial ribosomal protein L51 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1315447 Noxa1 NADPH oxidase activator 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20645308 1315451 Mllt6 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200402 MGI 1315451 Mllt6 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20220519 MGI 1315451 Mllt6 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210826 MGI 1315451 Mllt6 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 1315451 Mllt6 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1315451 Mllt6 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1315451 Mllt6 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1315451 Mllt6 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1315451 Mllt6 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21170927 1315451 Mllt6 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20220519 MGI 1315451 Mllt6 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20210826 MGI 1315451 Mllt6 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 1315451 Mllt6 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20220519 MGI 1315451 Mllt6 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 6 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20181227 MGI 1315453 Slc45a2 solute carrier family 45, member 2 gene MP:0000371 diluted coat color IEA N RGD:5509061 20111116 MGI 1315453 Slc45a2 solute carrier family 45, member 2 gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9864865 1315453 Slc45a2 solute carrier family 45, member 2 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1315453 Slc45a2 solute carrier family 45, member 2 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9864865 1315453 Slc45a2 solute carrier family 45, member 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20111116 MGI 1315453 Slc45a2 solute carrier family 45, member 2 gene MP:0001924 infertility IEA N RGD:5509061 20111116 MGI 1315453 Slc45a2 solute carrier family 45, member 2 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15238537 1315453 Slc45a2 solute carrier family 45, member 2 gene MP:0002095 abnormal skin pigmentation IEA N RGD:5509061 20111116 MGI 1315453 Slc45a2 solute carrier family 45, member 2 gene MP:0005172 decreased eye pigmentation IEA N RGD:5509061 20111116 MGI 1315453 Slc45a2 solute carrier family 45, member 2 gene MP:0005408 hypopigmentation IEA N RGD:5509061 20111116 MGI 1315453 Slc45a2 solute carrier family 45, member 2 gene MP:0008480 absent eye pigmentation IEA N RGD:5509061 20141003 MGI 1315453 Slc45a2 solute carrier family 45, member 2 gene MP:0009928 abnormal pinna hair pigmentation IEA N RGD:5509061 20141003 MGI 1315453 Slc45a2 solute carrier family 45, member 2 gene MP:0011627 decreased skin pigmentation IEA N RGD:5509061 20141003 MGI 1315456 Serpinf2 serine (or cysteine) peptidase inhibitor, clade F, member 2 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:10090937 1315456 Serpinf2 serine (or cysteine) peptidase inhibitor, clade F, member 2 gene MP:0003422 abnormal thrombolysis IAGP N RGD:5509061 20201001 MGI PMID:10090937 1315456 Serpinf2 serine (or cysteine) peptidase inhibitor, clade F, member 2 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20201001 MGI PMID:10318667 1315458 Bach1 BTB and CNC homology 1, basic leucine zipper transcription factor 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20220811 MGI 1315458 Bach1 BTB and CNC homology 1, basic leucine zipper transcription factor 1 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16824198 1315458 Bach1 BTB and CNC homology 1, basic leucine zipper transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12356737 1315458 Bach1 BTB and CNC homology 1, basic leucine zipper transcription factor 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 1315458 Bach1 BTB and CNC homology 1, basic leucine zipper transcription factor 1 gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16824198 1315458 Bach1 BTB and CNC homology 1, basic leucine zipper transcription factor 1 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20230601 MGI 1315458 Bach1 BTB and CNC homology 1, basic leucine zipper transcription factor 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:16824198 1315458 Bach1 BTB and CNC homology 1, basic leucine zipper transcription factor 1 gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20230601 MGI 1315458 Bach1 BTB and CNC homology 1, basic leucine zipper transcription factor 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16824198 1315458 Bach1 BTB and CNC homology 1, basic leucine zipper transcription factor 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1315458 Bach1 BTB and CNC homology 1, basic leucine zipper transcription factor 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1315458 Bach1 BTB and CNC homology 1, basic leucine zipper transcription factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1315458 Bach1 BTB and CNC homology 1, basic leucine zipper transcription factor 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:21632933 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:22974978 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:21632933 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18264090 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22974978 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18264090 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21632933 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22974978 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20150305 MGI PMID:25378165 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22974978 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18264090 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21632933 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0002635 reduced sensorimotor gating IAGP N RGD:5509061 20150305 MGI PMID:25378165 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:21632933 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:21632933 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:22974978 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18264090 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0002801 abnormal long-term object recognition memory IAGP N RGD:5509061 20150305 MGI PMID:25378165 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20150305 MGI PMID:25378165 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21632933 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:21632933 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:22974978 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18264090 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21632933 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21632933 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20150305 MGI PMID:25378165 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20150305 MGI PMID:25378165 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20150305 MGI PMID:25378165 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21632933 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21632933 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0009949 abnormal olfactory bulb granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21632933 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0009951 abnormal olfactory bulb mitral cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21632933 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0009952 abnormal olfactory bulb subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21632933 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22974978 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20150305 MGI PMID:25378165 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20150305 MGI PMID:25378165 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:25378165 1315459 Ccdc88a coiled coil domain containing 88A gene MP:0030956 abnormal neuronal precursor cell migration IAGP N RGD:5509061 20190725 MGI PMID:21632933 1315461 Pltp phospholipid transfer protein gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10079112 1315461 Pltp phospholipid transfer protein gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10079112 1315461 Pltp phospholipid transfer protein gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10079112 1315461 Pltp phospholipid transfer protein gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20170629 MGI PMID:23846500 1315461 Pltp phospholipid transfer protein gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:16467369 1315461 Pltp phospholipid transfer protein gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:21514421 1315461 Pltp phospholipid transfer protein gene MP:0001337 dry eyes IAGP N RGD:5509061 20141003 MGI PMID:21514421 1315461 Pltp phospholipid transfer protein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:16467369 1315461 Pltp phospholipid transfer protein gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20170629 MGI PMID:23846500 1315461 Pltp phospholipid transfer protein gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:16467369 1315461 Pltp phospholipid transfer protein gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:16467369 1315461 Pltp phospholipid transfer protein gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16467369 1315461 Pltp phospholipid transfer protein gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20170629 MGI PMID:23846500 1315461 Pltp phospholipid transfer protein gene MP:0003981 decreased circulating phospholipid level IAGP N RGD:5509061 20170629 MGI PMID:23846500 1315461 Pltp phospholipid transfer protein gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:16467369 1315461 Pltp phospholipid transfer protein gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:10079112 1315461 Pltp phospholipid transfer protein gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10079112 1315461 Pltp phospholipid transfer protein gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20170629 MGI PMID:23846500 1315461 Pltp phospholipid transfer protein gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:21514421 1315461 Pltp phospholipid transfer protein gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21514421 1315461 Pltp phospholipid transfer protein gene MP:0011231 abnormal vitamin E level IAGP N RGD:5509061 20141003 MGI PMID:16467369 1315461 Pltp phospholipid transfer protein gene MP:0020126 decreased circulating HDL phospholipid level IAGP N RGD:5509061 20170629 MGI PMID:23846500 1315461 Pltp phospholipid transfer protein gene MP:0020129 decreased circulating non-HDL phospholipid level IAGP N RGD:5509061 20170629 MGI PMID:23846500 1315461 Pltp phospholipid transfer protein gene MP:0020151 abnormal circulating non-HDL cholesterol level IAGP N RGD:5509061 20170629 MGI PMID:23846500 1315461 Pltp phospholipid transfer protein gene MP:0020854 increased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:21514421 1315461 Pltp phospholipid transfer protein gene MP:0020859 disorganized cornea epithelium IAGP N RGD:5509061 20181101 MGI PMID:21514421 1315461 Pltp phospholipid transfer protein gene MP:0031432 cornea perforation IAGP N RGD:5509061 20220721 MGI PMID:21514421 1315463 Abcc10 ATP-binding cassette, sub-family C member 10 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1315463 Abcc10 ATP-binding cassette, sub-family C member 10 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21576088 1315463 Abcc10 ATP-binding cassette, sub-family C member 10 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21576088 1315463 Abcc10 ATP-binding cassette, sub-family C member 10 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:21576088 1315463 Abcc10 ATP-binding cassette, sub-family C member 10 gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21576088 1315463 Abcc10 ATP-binding cassette, sub-family C member 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21576088 1315463 Abcc10 ATP-binding cassette, sub-family C member 10 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:21576088 1315463 Abcc10 ATP-binding cassette, sub-family C member 10 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:21576088 1315463 Abcc10 ATP-binding cassette, sub-family C member 10 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:21576088 1315463 Abcc10 ATP-binding cassette, sub-family C member 10 gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:21576088 1315463 Abcc10 ATP-binding cassette, sub-family C member 10 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21576088 1315463 Abcc10 ATP-binding cassette, sub-family C member 10 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21576088 1315463 Abcc10 ATP-binding cassette, sub-family C member 10 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 1315464 Wdr91 WD repeat domain 91 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20191114 MGI PMID:28860274 1315464 Wdr91 WD repeat domain 91 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20191114 MGI PMID:28860274 1315464 Wdr91 WD repeat domain 91 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20220519 MGI 1315464 Wdr91 WD repeat domain 91 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20191114 MGI PMID:28860274 1315464 Wdr91 WD repeat domain 91 gene MP:0002083 premature death IAGP N RGD:5509061 20191114 MGI PMID:28860274 1315464 Wdr91 WD repeat domain 91 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20191114 MGI PMID:28860274 1315464 Wdr91 WD repeat domain 91 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20191114 MGI PMID:28860274 1315464 Wdr91 WD repeat domain 91 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20191114 MGI PMID:28860274 1315464 Wdr91 WD repeat domain 91 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20191114 MGI PMID:28860274 1315464 Wdr91 WD repeat domain 91 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20191114 MGI PMID:28860274 1315464 Wdr91 WD repeat domain 91 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20191114 MGI PMID:28860274 1315464 Wdr91 WD repeat domain 91 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20191114 MGI PMID:28860274 1315464 Wdr91 WD repeat domain 91 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0001573 abnormal circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0002424 abnormal reticulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0010072 increased pruritus IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:23077570 1315465 Mcat malonyl CoA:ACP acyltransferase (mitochondrial) gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:23077570 1315467 Fhod1 formin homology 2 domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201001 MGI PMID:31008549 1315467 Fhod1 formin homology 2 domain containing 1 gene MP:0002626 increased heart rate IEA N RGD:5509061 20210826 MGI 1315467 Fhod1 formin homology 2 domain containing 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220519 MGI 1315467 Fhod1 formin homology 2 domain containing 1 gene MP:0010507 shortened RR interval IEA N RGD:5509061 20210826 MGI 1315469 Zfp385a zinc finger protein 385A gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11927637 1315469 Zfp385a zinc finger protein 385A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11927637 1315469 Zfp385a zinc finger protein 385A gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11927637 1315469 Zfp385a zinc finger protein 385A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10585558 1315469 Zfp385a zinc finger protein 385A gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11927637 1315469 Zfp385a zinc finger protein 385A gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:11927637 1315469 Zfp385a zinc finger protein 385A gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:11927637 1315469 Zfp385a zinc finger protein 385A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11927637 1315469 Zfp385a zinc finger protein 385A gene MP:0020431 decreased platelet alpha-granule number IAGP N RGD:5509061 20170803 MGI PMID:11927637 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:16571658 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:22194846 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0000018 small ears IAGP N RGD:5509061 20151112 MGI PMID:26234751 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:16571658 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:22194846 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20151112 MGI PMID:26234751 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:16571658 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0000585 kinked tail IAGP N RGD:5509061 20151112 MGI PMID:26234751 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0000753 paralysis IAGP N RGD:5509061 20151112 MGI PMID:26234751 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16571658 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22194846 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16571658 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0001265 decreased body size IAGP N RGD:5509061 20151112 MGI PMID:26234751 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22194846 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0001921 reduced fertility IAGP N RGD:5509061 20151112 MGI PMID:26234751 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0001924 infertility IEA N RGD:5509061 20141003 MGI 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0001925 male infertility IEA N RGD:5509061 20230601 MGI 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:22194846 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0002083 premature death IAGP N RGD:5509061 20151112 MGI PMID:26234751 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20200514 MGI 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:16571658 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20151112 MGI PMID:26234751 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:22194846 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:22194846 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0004477 turbinate hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16571658 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16571658 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210520 MGI 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0005323 dystonia IAGP N RGD:5509061 20151112 MGI PMID:26234751 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20200514 MGI 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0006033 abnormal external auditory canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16571658 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0006325 impaired hearing IAGP N RGD:5509061 20151112 MGI PMID:26234751 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20160609 MGI PMID:26234751 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0010052 increased grip strength IEA N RGD:5509061 20200514 MGI 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20151112 MGI PMID:26234751 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18634873 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16571658 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:22194846 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0030188 round snout IAGP N RGD:5509061 20171019 MGI PMID:16571658 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0030258 small mandibular condyloid process IAGP N RGD:5509061 20171019 MGI PMID:22194846 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0030261 abnormal temporal bone zygomatic process morphology IAGP N RGD:5509061 20171214 MGI PMID:22194846 1315477 Prkra protein kinase, interferon inducible double stranded RNA dependent activator gene MP:0030283 small mandibular coronoid process IAGP N RGD:5509061 20171102 MGI PMID:22194846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10934170 1315479 Traf4 TNF receptor associated factor 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:10934170 1315479 Traf4 TNF receptor associated factor 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18284467 1315479 Traf4 TNF receptor associated factor 4 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:18284467 1315479 Traf4 TNF receptor associated factor 4 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:10934170 1315479 Traf4 TNF receptor associated factor 4 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0004549 small trachea IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0004552 fused tracheal cartilage rings IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:18773073 1315479 Traf4 TNF receptor associated factor 4 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0010883 trachea stenosis IAGP N RGD:5509061 20150212 MGI PMID:10934170 1315479 Traf4 TNF receptor associated factor 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18773073 1315479 Traf4 TNF receptor associated factor 4 gene MP:0012547 spina bifida cystica IAGP N RGD:5509061 20141003 MGI PMID:11943846 1315479 Traf4 TNF receptor associated factor 4 gene MP:0013752 stridor IAGP N RGD:5509061 20150416 MGI PMID:10934170 1315479 Traf4 TNF receptor associated factor 4 gene MP:0031086 wheezing IAGP N RGD:5509061 20200709 MGI PMID:11943846 1315486 Atp8b4 ATPase, class I, type 8B, member 4 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1315486 Atp8b4 ATPase, class I, type 8B, member 4 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1315486 Atp8b4 ATPase, class I, type 8B, member 4 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230601 MGI 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20160512 MGI PMID:25712208 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20160512 MGI PMID:25712208 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160512 MGI PMID:25712208 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0001586 abnormal erythrocyte cell number IAGP N RGD:5509061 20160512 MGI PMID:25712208 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0002309 abnormal vital capacity IAGP N RGD:5509061 20160512 MGI PMID:25712208 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20160616 MGI PMID:25712208 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20161027 MGI PMID:25843683 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20160512 MGI PMID:25712208 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20161027 MGI PMID:25843683 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20160512 MGI PMID:25712208 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0005585 increased tidal volume IAGP N RGD:5509061 20160512 MGI PMID:25712208 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0010042 abnormal oval cell physiology IAGP N RGD:5509061 20161027 MGI PMID:25843683 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0010896 decreased lung compliance IAGP N RGD:5509061 20160512 MGI PMID:25712208 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0010936 decreased airway resistance IAGP N RGD:5509061 20160512 MGI PMID:25712208 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0010937 increased total lung capacity IAGP N RGD:5509061 20160512 MGI PMID:25712208 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0014275 increased respiration IAGP N RGD:5509061 20230810 MGI PMID:25712208 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0020253 increased collagen level IAGP N RGD:5509061 20161027 MGI PMID:25843683 1315488 Adamts7 ADAM metallopeptidase with thrombospondin type 1 motif 7 gene MP:0020316 decreased vascular endothelial cell proliferation IAGP N RGD:5509061 20160616 MGI PMID:25712208 1315492 Rev1 REV1, DNA directed polymerase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16476771 1315492 Rev1 REV1, DNA directed polymerase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15653636 1315492 Rev1 REV1, DNA directed polymerase gene MP:0002223 lymphoid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16476771 1315492 Rev1 REV1, DNA directed polymerase gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:16476771 1315492 Rev1 REV1, DNA directed polymerase gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:19587019 1315492 Rev1 REV1, DNA directed polymerase gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16476771 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:20375278 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9590289 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18400300 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12794146 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:9590289 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20375278 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20375278 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20201022 MGI 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:20375278 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:16943797 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:16943797 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:16943797 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:9590289 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:9590289 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:16943797 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:16943797 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160421 MGI 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:20375278 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20375278 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0011369 increased renal glomerulus apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9590289 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:9590289 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0014375 increased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:20375278 1315494 C1qa complement component 1, q subcomponent, alpha polypeptide gene MP:0014378 increased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:20375278 1315495 Nat10 N-acetyltransferase 10 gene MP:0000160 kyphosis IAGP N RGD:5509061 20220721 MGI PMID:29703891 1315495 Nat10 N-acetyltransferase 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220721 MGI PMID:29703891 1315495 Nat10 N-acetyltransferase 10 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20220721 MGI PMID:29703891 1315495 Nat10 N-acetyltransferase 10 gene MP:0002083 premature death IAGP N RGD:5509061 20220721 MGI PMID:29703891 1315495 Nat10 N-acetyltransferase 10 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20220721 MGI PMID:29703891 1315495 Nat10 N-acetyltransferase 10 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20220721 MGI PMID:29703891 1315497 Adgrf4 adhesion G protein-coupled receptor F4 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20220811 MGI 1315498 Nudt7 nudix hydrolase 7 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20191128 MGI PMID:30143643 1315498 Nudt7 nudix hydrolase 7 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20191128 MGI PMID:30143643 1315498 Nudt7 nudix hydrolase 7 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20191128 MGI PMID:30143643 1315498 Nudt7 nudix hydrolase 7 gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20191128 MGI PMID:30143643 1315498 Nudt7 nudix hydrolase 7 gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20191128 MGI PMID:30143643 1315498 Nudt7 nudix hydrolase 7 gene MP:0020847 abnormal peroxisome physiology IAGP N RGD:5509061 20191128 MGI PMID:30143643 1315500 Mrps35 mitochondrial ribosomal protein S35 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1315500 Mrps35 mitochondrial ribosomal protein S35 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160804 MGI 1315500 Mrps35 mitochondrial ribosomal protein S35 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20160804 MGI 1315509 Six4 sine oculis-related homeobox 4 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15955062 1315509 Six4 sine oculis-related homeobox 4 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0001512 trunk curl IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11313460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0003142 anotia IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0004422 small temporal bone IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0006211 small orbits IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0006284 absent hypaxial muscle IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15955062 1315509 Six4 sine oculis-related homeobox 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0013929 absent eye muscles IAGP N RGD:5509061 20171026 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0013964 absent tongue muscles IAGP N RGD:5509061 20171026 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0030208 abnormal intrinsic tongue muscle morphology IAGP N RGD:5509061 20171026 MGI PMID:15788460 1315509 Six4 sine oculis-related homeobox 4 gene MP:0030210 abnormal genioglossus muscle morphology IAGP N RGD:5509061 20171026 MGI PMID:15788460 1315511 B3galt5 UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 5 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1315514 Bicdl2 BICD family like cargo adaptor 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1315514 Bicdl2 BICD family like cargo adaptor 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1315514 Bicdl2 BICD family like cargo adaptor 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1315514 Bicdl2 BICD family like cargo adaptor 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1315516 Mcmbp minichromosome maintenance complex binding protein gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1315516 Mcmbp minichromosome maintenance complex binding protein gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1315516 Mcmbp minichromosome maintenance complex binding protein gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20221215 MGI 1315516 Mcmbp minichromosome maintenance complex binding protein gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1315516 Mcmbp minichromosome maintenance complex binding protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315516 Mcmbp minichromosome maintenance complex binding protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1315518 Nrap nebulin-related anchoring protein gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20211021 MGI 1315519 Sigirr single immunoglobulin and toll-interleukin 1 receptor (TIR) domain gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12925853 1315519 Sigirr single immunoglobulin and toll-interleukin 1 receptor (TIR) domain gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14993616 1315519 Sigirr single immunoglobulin and toll-interleukin 1 receptor (TIR) domain gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:14993616 1315519 Sigirr single immunoglobulin and toll-interleukin 1 receptor (TIR) domain gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:14993616 1315519 Sigirr single immunoglobulin and toll-interleukin 1 receptor (TIR) domain gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:14993616 1315519 Sigirr single immunoglobulin and toll-interleukin 1 receptor (TIR) domain gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:12925853 1315519 Sigirr single immunoglobulin and toll-interleukin 1 receptor (TIR) domain gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:14993616 1315519 Sigirr single immunoglobulin and toll-interleukin 1 receptor (TIR) domain gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12925853 1315519 Sigirr single immunoglobulin and toll-interleukin 1 receptor (TIR) domain gene MP:0009334 abnormal splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12925853 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0002710 increased glucagon secretion IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20160707 MGI PMID:26086111 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0009180 increased pancreatic delta cell number IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20160707 MGI PMID:26086111 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0014117 increased pancreatic beta cell apoptosis IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315526 Aldh1b1 aldehyde dehydrogenase 1 family, member B1 gene MP:0014121 increased pancreatic islet cell apoptosis IAGP N RGD:5509061 20161013 MGI PMID:26518685 1315528 Tfcp2 transcription factor CP2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10995745 1315530 Cabcoco1 ciliary associated calcium binding coiled-coil 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1315530 Cabcoco1 ciliary associated calcium binding coiled-coil 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1315530 Cabcoco1 ciliary associated calcium binding coiled-coil 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1315530 Cabcoco1 ciliary associated calcium binding coiled-coil 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20240307 MGI PMID:37601242 1315530 Cabcoco1 ciliary associated calcium binding coiled-coil 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20240307 MGI PMID:37601242 1315530 Cabcoco1 ciliary associated calcium binding coiled-coil 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240307 MGI PMID:37601242 1315530 Cabcoco1 ciliary associated calcium binding coiled-coil 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240307 MGI PMID:37601242 1315530 Cabcoco1 ciliary associated calcium binding coiled-coil 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1315530 Cabcoco1 ciliary associated calcium binding coiled-coil 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1315530 Cabcoco1 ciliary associated calcium binding coiled-coil 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20240307 MGI PMID:37601242 1315530 Cabcoco1 ciliary associated calcium binding coiled-coil 1 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20240307 MGI PMID:37601242 1315530 Cabcoco1 ciliary associated calcium binding coiled-coil 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20240307 MGI PMID:37601242 1315530 Cabcoco1 ciliary associated calcium binding coiled-coil 1 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20240307 MGI PMID:37601242 1315530 Cabcoco1 ciliary associated calcium binding coiled-coil 1 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20240307 MGI PMID:37601242 1315530 Cabcoco1 ciliary associated calcium binding coiled-coil 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1315533 Clmn calmin gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0008599 increased circulating interleukin-2 level IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20190912 MGI PMID:31036553 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0011164 panniculitis IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315536 Mta2 metastasis-associated gene family, member 2 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18353770 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200402 MGI 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0000503 excessive digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:17030183 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17030183 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:17030183 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19213841 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:17030183 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17030183 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17030183 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:19213841 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17030183 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19213841 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0006003 abnormal large intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:17030183 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20181227 MGI 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0011082 abnormal gastrointestinal motility IAGP N RGD:5509061 20141003 MGI PMID:17030183 1315540 Gpr39 G protein-coupled receptor 39 gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:17030183 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000239 absent common myeloid progenitor cells IAGP N RGD:5509061 20141003 MGI PMID:7830794 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12552125 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:7624372 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:7830794 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:12552125 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000416 sparse hair IEA N RGD:5509061 20141003 MGI 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0000418 focal hair loss IEA N RGD:5509061 20141003 MGI 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20141003 MGI 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12540851 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12552125 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7830794 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12552125 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:7830794 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7830794 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:7624372 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:7624372 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20141003 MGI PMID:7624372 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20141003 MGI PMID:7830794 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:7624372 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:7624372 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:7624372 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12540851 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:12552125 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22401818 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12552125 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:12552125 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12552125 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12540851 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12552125 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7624372 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7830794 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:7624372 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:7830794 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7624372 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7830794 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22401818 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:16675709 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:7830794 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:12552125 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0009328 delayed heart looping IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1836514 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10572089 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7624372 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7830794 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18550854 1315544 Tal1 T cell acute lymphocytic leukemia 1 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:7830794 1315551 Pigk phosphatidylinositol glycan anchor biosynthesis, class K gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20240523 MGI 1315551 Pigk phosphatidylinositol glycan anchor biosynthesis, class K gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20230810 MGI PMID:33392778 1315551 Pigk phosphatidylinositol glycan anchor biosynthesis, class K gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315551 Pigk phosphatidylinositol glycan anchor biosynthesis, class K gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1315556 Tbcc tubulin-specific chaperone C gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20240926 MGI 1315556 Tbcc tubulin-specific chaperone C gene MP:0004964 absent inner cell mass IEA N RGD:5509061 20240926 MGI 1315556 Tbcc tubulin-specific chaperone C gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220519 MGI 1315556 Tbcc tubulin-specific chaperone C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1315556 Tbcc tubulin-specific chaperone C gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1315556 Tbcc tubulin-specific chaperone C gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240926 MGI 1315558 Rnf125 ring finger protein 125 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1315560 Gtpbp1 GTP binding protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10938096 1315566 Prodh2 proline dehydrogenase (oxidase) 2 gene MP:0006272 abnormal urine organic anion level IAGP N RGD:5509061 20201210 MGI PMID:31821850 1315566 Prodh2 proline dehydrogenase (oxidase) 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20201210 MGI PMID:31821850 1315566 Prodh2 proline dehydrogenase (oxidase) 2 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20201210 MGI PMID:31821850 1315566 Prodh2 proline dehydrogenase (oxidase) 2 gene MP:0011517 hyperoxaluria IAGP N RGD:5509061 20201210 MGI PMID:31821850 1315566 Prodh2 proline dehydrogenase (oxidase) 2 gene MP:0030681 increased circulating hydroxyproline level IAGP N RGD:5509061 20201210 MGI PMID:31821850 1315566 Prodh2 proline dehydrogenase (oxidase) 2 gene MP:0030682 hydroxyprolinuria IAGP N RGD:5509061 20201210 MGI PMID:31821850 1315570 Kdelr1 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20141003 MGI 1315570 Kdelr1 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20151022 MGI PMID:26438836 1315570 Kdelr1 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20151022 MGI PMID:26438836 1315570 Kdelr1 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20151022 MGI PMID:26438836 1315570 Kdelr1 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20151022 MGI PMID:26438836 1315570 Kdelr1 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20151022 MGI PMID:26438836 1315570 Kdelr1 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1 gene MP:0008041 absent NK T cells IAGP N RGD:5509061 20151022 MGI PMID:26438836 1315570 Kdelr1 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20151022 MGI PMID:26438836 1315570 Kdelr1 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20151022 MGI PMID:26438836 1315570 Kdelr1 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20151022 MGI PMID:26438836 1315570 Kdelr1 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20151022 MGI PMID:26438836 1315570 Kdelr1 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1 gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20151022 MGI PMID:26438836 1315570 Kdelr1 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1 gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20151022 MGI PMID:26438836 1315570 Kdelr1 KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:26438836 1315578 S100a16 S100 calcium binding protein A16 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1315578 S100a16 S100 calcium binding protein A16 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1315578 S100a16 S100 calcium binding protein A16 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20201022 MGI 1315578 S100a16 S100 calcium binding protein A16 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20221222 MGI PMID:35914619 1315578 S100a16 S100 calcium binding protein A16 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20221222 MGI PMID:35914619 1315578 S100a16 S100 calcium binding protein A16 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20221222 MGI PMID:35914619 1315578 S100a16 S100 calcium binding protein A16 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20221222 MGI PMID:35914619 1315578 S100a16 S100 calcium binding protein A16 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1315582 Ube3d ubiquitin protein ligase E3D gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20170314 MGI PMID:25872646 1315582 Ube3d ubiquitin protein ligase E3D gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20170314 MGI PMID:25872646 1315582 Ube3d ubiquitin protein ligase E3D gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20170314 MGI PMID:25872646 1315585 Glmn glomulin, FKBP associated protein gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20210930 MGI PMID:33905568 1315585 Glmn glomulin, FKBP associated protein gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:22405651 1315585 Glmn glomulin, FKBP associated protein gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0001722 pale yolk sac IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:22405651 1315585 Glmn glomulin, FKBP associated protein gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22405651 1315585 Glmn glomulin, FKBP associated protein gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:22405651 1315585 Glmn glomulin, FKBP associated protein gene MP:0002824 abnormal chorioallantoic fusion IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0002861 abnormal tail bud morphology IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0003717 pallor IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22405651 1315585 Glmn glomulin, FKBP associated protein gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:22405651 1315585 Glmn glomulin, FKBP associated protein gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22405651 1315585 Glmn glomulin, FKBP associated protein gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0008854 bleb IEA N RGD:5509061 20221215 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22405651 1315585 Glmn glomulin, FKBP associated protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1315585 Glmn glomulin, FKBP associated protein gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:22405651 1315585 Glmn glomulin, FKBP associated protein gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1315589 Rorb RAR-related orphan receptor beta gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20170803 MGI PMID:25296752 1315589 Rorb RAR-related orphan receptor beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9670004 1315589 Rorb RAR-related orphan receptor beta gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:9670004 1315589 Rorb RAR-related orphan receptor beta gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:9670004 1315589 Rorb RAR-related orphan receptor beta gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:9670004 1315589 Rorb RAR-related orphan receptor beta gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20230727 MGI PMID:37300435 1315589 Rorb RAR-related orphan receptor beta gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9670004 1315589 Rorb RAR-related orphan receptor beta gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23652001 1315589 Rorb RAR-related orphan receptor beta gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9670004 1315589 Rorb RAR-related orphan receptor beta gene MP:0001406 abnormal gait IAGP N RGD:5509061 20230720 MGI PMID:37300435 1315589 Rorb RAR-related orphan receptor beta gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:9670004 1315589 Rorb RAR-related orphan receptor beta gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:9670004 1315589 Rorb RAR-related orphan receptor beta gene MP:0001524 impaired limb coordination IEA N RGD:5509061 20150702 MGI 1315589 Rorb RAR-related orphan receptor beta gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 1315589 Rorb RAR-related orphan receptor beta gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:9670004 1315589 Rorb RAR-related orphan receptor beta gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:9670004 1315589 Rorb RAR-related orphan receptor beta gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1315589 Rorb RAR-related orphan receptor beta gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:9670004 1315589 Rorb RAR-related orphan receptor beta gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:9670004 1315589 Rorb RAR-related orphan receptor beta gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20230727 MGI PMID:37300435 1315589 Rorb RAR-related orphan receptor beta gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:23652001 1315589 Rorb RAR-related orphan receptor beta gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20230727 MGI PMID:37300435 1315589 Rorb RAR-related orphan receptor beta gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20230727 MGI PMID:37300435 1315589 Rorb RAR-related orphan receptor beta gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23652001 1315589 Rorb RAR-related orphan receptor beta gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20170803 MGI PMID:25296752 1315589 Rorb RAR-related orphan receptor beta gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20170803 MGI PMID:25296752 1315589 Rorb RAR-related orphan receptor beta gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20170803 MGI PMID:25296752 1315589 Rorb RAR-related orphan receptor beta gene MP:0005241 abnormal retina ganglion layer morphology IEA N RGD:5509061 20160428 MGI 1315589 Rorb RAR-related orphan receptor beta gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:9670004 1315589 Rorb RAR-related orphan receptor beta gene MP:0005551 abnormal eye electrophysiology IEA N RGD:5509061 20160428 MGI 1315589 Rorb RAR-related orphan receptor beta gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:9670004 1315589 Rorb RAR-related orphan receptor beta gene MP:0006095 absent amacrine cells IAGP N RGD:5509061 20141003 MGI PMID:23652001 1315589 Rorb RAR-related orphan receptor beta gene MP:0006095 absent amacrine cells IAGP N RGD:5509061 20170803 MGI PMID:25296752 1315589 Rorb RAR-related orphan receptor beta gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23652001 1315589 Rorb RAR-related orphan receptor beta gene MP:0008107 absent retina horizontal cells IAGP N RGD:5509061 20141003 MGI PMID:23652001 1315589 Rorb RAR-related orphan receptor beta gene MP:0008107 absent retina horizontal cells IAGP N RGD:5509061 20170803 MGI PMID:25296752 1315589 Rorb RAR-related orphan receptor beta gene MP:0008445 increased retina cone cell number IAGP N RGD:5509061 20170803 MGI PMID:25296752 1315589 Rorb RAR-related orphan receptor beta gene MP:0008448 abnormal retina cone cell inner segment morphology IAGP N RGD:5509061 20230727 MGI PMID:37300435 1315589 Rorb RAR-related orphan receptor beta gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20230727 MGI PMID:37300435 1315589 Rorb RAR-related orphan receptor beta gene MP:0008450 retina photoreceptor degeneration IEA N RGD:5509061 20160428 MGI 1315589 Rorb RAR-related orphan receptor beta gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20170803 MGI PMID:25296752 1315589 Rorb RAR-related orphan receptor beta gene MP:0008454 absent retina rod cells IAGP N RGD:5509061 20170803 MGI PMID:25296752 1315589 Rorb RAR-related orphan receptor beta gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:23652001 1315589 Rorb RAR-related orphan receptor beta gene MP:0008520 disorganized retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:23652001 1315589 Rorb RAR-related orphan receptor beta gene MP:0008520 disorganized retina outer plexiform layer IAGP N RGD:5509061 20170803 MGI PMID:25296752 1315589 Rorb RAR-related orphan receptor beta gene MP:0008581 disorganized photoreceptor inner segment IAGP N RGD:5509061 20230727 MGI PMID:37300435 1315589 Rorb RAR-related orphan receptor beta gene MP:0008583 absent photoreceptor inner segment IAGP N RGD:5509061 20170803 MGI PMID:25296752 1315589 Rorb RAR-related orphan receptor beta gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20170803 MGI PMID:25296752 1315589 Rorb RAR-related orphan receptor beta gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20230727 MGI PMID:37300435 1315589 Rorb RAR-related orphan receptor beta gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:23652001 1315589 Rorb RAR-related orphan receptor beta gene MP:0031606 increased susceptibility to age-related retinal degeneration IEA N RGD:5509061 20240404 MGI 1315591 Nav1 neuron navigator 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1315591 Nav1 neuron navigator 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1315591 Nav1 neuron navigator 1 gene MP:0000774 decreased brain size IEA N RGD:5509061 20210520 MGI 1315591 Nav1 neuron navigator 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1315591 Nav1 neuron navigator 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1315591 Nav1 neuron navigator 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1315591 Nav1 neuron navigator 1 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210520 MGI 1315591 Nav1 neuron navigator 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1315591 Nav1 neuron navigator 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1315591 Nav1 neuron navigator 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1315591 Nav1 neuron navigator 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1315591 Nav1 neuron navigator 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11352070 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11463376 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:11352070 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:11352070 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11352070 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11463376 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:11463376 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11352070 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11463376 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11463376 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11352070 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:11352070 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:11463376 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:11352070 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11352070 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11463376 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:11352070 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:11352070 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:11463376 1315593 Tbpl1 TATA box binding protein-like 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:11352070 1315600 Dmwd dystrophia myotonica-containing WD repeat motif gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1315600 Dmwd dystrophia myotonica-containing WD repeat motif gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1315600 Dmwd dystrophia myotonica-containing WD repeat motif gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:24086156 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0000379 decreased hair follicle number IEA N RGD:5509061 20220707 MGI 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0000384 distorted hair follicle pattern IAGP N RGD:5509061 20150709 MGI PMID:24721909 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12067728 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20190124 MGI PMID:25340873 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22464327 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0000588 thick tail IAGP N RGD:5509061 20141003 MGI PMID:12067728 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:24086156 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20190124 MGI PMID:25340873 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:12067728 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20150709 MGI PMID:24721909 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20190124 MGI PMID:25340873 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:12067728 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:12067728 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20150709 MGI PMID:24721909 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12067728 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:12067728 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20141003 MGI 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24086156 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:24086156 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:24086156 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20190124 MGI PMID:25340873 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:12067728 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24086156 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20141003 MGI 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22464327 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22464327 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:12067728 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:24086156 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0003164 decreased posterior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:24086156 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0003413 hair follicle degeneration IEA N RGD:5509061 20220707 MGI 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:12067728 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:12067728 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0003809 abnormal hair shaft morphology IEA N RGD:5509061 20220714 MGI 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0004425 abnormal otolith organ morphology IAGP N RGD:5509061 20141003 MGI PMID:24086156 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:24086156 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0008861 abnormal hair shedding IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0008861 abnormal hair shedding IAGP N RGD:5509061 20190124 MGI PMID:25340873 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0009545 abnormal dermis papillary layer morphology IEA N RGD:5509061 20220714 MGI 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12067728 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0010678 abnormal skin adnexa morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0010686 abnormal hair follicle matrix region morphology IEA N RGD:5509061 20220714 MGI 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24086156 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0011238 abnormal inner ear development IAGP N RGD:5509061 20141003 MGI PMID:24086156 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:24086156 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:24086156 1315603 Lrig1 leucine-rich repeats and immunoglobulin-like domains 1 gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:24086156 1315605 Mex3b mex3 RNA binding family member B gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20200514 MGI 1315605 Mex3b mex3 RNA binding family member B gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20200514 MGI 1315605 Mex3b mex3 RNA binding family member B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160526 MGI PMID:24803656 1315605 Mex3b mex3 RNA binding family member B gene MP:0001265 decreased body size IAGP N RGD:5509061 20160526 MGI PMID:24803656 1315605 Mex3b mex3 RNA binding family member B gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1315605 Mex3b mex3 RNA binding family member B gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20160526 MGI PMID:24803656 1315605 Mex3b mex3 RNA binding family member B gene MP:0001921 reduced fertility IAGP N RGD:5509061 20160526 MGI PMID:24803656 1315605 Mex3b mex3 RNA binding family member B gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20160526 MGI PMID:24803656 1315605 Mex3b mex3 RNA binding family member B gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20200514 MGI 1315605 Mex3b mex3 RNA binding family member B gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1315605 Mex3b mex3 RNA binding family member B gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20160526 MGI PMID:24803656 1315605 Mex3b mex3 RNA binding family member B gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20160526 MGI PMID:24803656 1315605 Mex3b mex3 RNA binding family member B gene MP:0002776 increased Sertoli cell number IAGP N RGD:5509061 20160526 MGI PMID:24803656 1315605 Mex3b mex3 RNA binding family member B gene MP:0003036 vertebral transformation IEA N RGD:5509061 20200514 MGI 1315605 Mex3b mex3 RNA binding family member B gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20200514 MGI 1315605 Mex3b mex3 RNA binding family member B gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20160526 MGI PMID:24803656 1315605 Mex3b mex3 RNA binding family member B gene MP:0009853 decreased Sertoli cell phagocytosis IAGP N RGD:5509061 20160526 MGI PMID:24803656 1315605 Mex3b mex3 RNA binding family member B gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20160526 MGI PMID:24803656 1315605 Mex3b mex3 RNA binding family member B gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20160526 MGI PMID:24803656 1315605 Mex3b mex3 RNA binding family member B gene MP:0020142 increased anti-sperm antibody level IAGP N RGD:5509061 20160616 MGI PMID:24803656 1315605 Mex3b mex3 RNA binding family member B gene MP:0020355 abnormal Sertoli cell barrier morphology IAGP N RGD:5509061 20160915 MGI PMID:24803656 1315605 Mex3b mex3 RNA binding family member B gene MP:0020356 abnormal Sertoli cell barrier function IAGP N RGD:5509061 20160915 MGI PMID:24803656 1315605 Mex3b mex3 RNA binding family member B gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20160421 MGI 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20160811 MGI 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20160225 MGI PMID:25480920 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20160225 MGI PMID:25480920 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20160225 MGI PMID:25480920 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160225 MGI PMID:25480920 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20160225 MGI PMID:25480920 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20160811 MGI 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20160421 MGI 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160707 MGI PMID:25620209 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0002583 absent extraembryonic ectoderm IAGP N RGD:5509061 20170629 MGI PMID:25480920 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20170629 MGI PMID:25480920 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20160225 MGI PMID:25480920 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20190502 MGI 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160225 MGI PMID:25480920 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20170629 MGI PMID:25480920 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0011191 increased embryonic epiblast cell apoptosis IAGP N RGD:5509061 20170629 MGI PMID:25480920 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0012159 absent anterior visceral endoderm IAGP N RGD:5509061 20170629 MGI PMID:25480920 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1315611 Chd1 chromodomain helicase DNA binding protein 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1315615 Enam enamelin gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0000122 premature tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:18252720 1315615 Enam enamelin gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1315615 Enam enamelin gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1315615 Enam enamelin gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20141003 MGI PMID:18252720 1315615 Enam enamelin gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20210520 MGI 1315615 Enam enamelin gene MP:0001258 decreased body length IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:15649948 1315615 Enam enamelin gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20160304 MGI PMID:24603688 1315615 Enam enamelin gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:15649948 1315615 Enam enamelin gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:18252720 1315615 Enam enamelin gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20160304 MGI PMID:24603688 1315615 Enam enamelin gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20141003 MGI PMID:15271968 1315615 Enam enamelin gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20160304 MGI PMID:24603688 1315615 Enam enamelin gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0002649 abnormal enamel rod pattern IAGP N RGD:5509061 20160304 MGI PMID:24603688 1315615 Enam enamelin gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20160304 MGI PMID:24603688 1315615 Enam enamelin gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:18252720 1315615 Enam enamelin gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20160304 MGI PMID:24603688 1315615 Enam enamelin gene MP:0002817 abnormal tooth mineralization IAGP N RGD:5509061 20160304 MGI PMID:24603688 1315615 Enam enamelin gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0003053 delayed tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:18252720 1315615 Enam enamelin gene MP:0003404 absent enamel IAGP N RGD:5509061 20141003 MGI PMID:15271968 1315615 Enam enamelin gene MP:0003404 absent enamel IAGP N RGD:5509061 20141003 MGI PMID:15649948 1315615 Enam enamelin gene MP:0003404 absent enamel IAGP N RGD:5509061 20141003 MGI PMID:18252720 1315615 Enam enamelin gene MP:0003404 absent enamel IAGP N RGD:5509061 20160304 MGI PMID:24603688 1315615 Enam enamelin gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0003932 abnormal molar crown morphology IAGP N RGD:5509061 20180125 MGI PMID:18252720 1315615 Enam enamelin gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:15649948 1315615 Enam enamelin gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:18252720 1315615 Enam enamelin gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20160304 MGI PMID:24603688 1315615 Enam enamelin gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0008851 decreased hemoglobin concentration distribution width IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1315615 Enam enamelin gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0010096 abnormal incisor color IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0010096 abnormal incisor color IAGP N RGD:5509061 20171005 MGI PMID:18252720 1315615 Enam enamelin gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0010747 abnormal enamel organ morphology IAGP N RGD:5509061 20160304 MGI PMID:24603688 1315615 Enam enamelin gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0011894 decreased circulating transferrin level IAGP N RGD:5509061 20151112 MGI PMID:22813216 1315615 Enam enamelin gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:18252720 1315615 Enam enamelin gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:24603688 1315615 Enam enamelin gene MP:0030137 abnormal upper incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:18252720 1315615 Enam enamelin gene MP:0030138 abnormal lower incisor color IAGP N RGD:5509061 20171005 MGI PMID:18252720 1315615 Enam enamelin gene MP:0030139 abnormal upper incisor color IAGP N RGD:5509061 20171005 MGI PMID:15271968 1315615 Enam enamelin gene MP:0030139 abnormal upper incisor color IAGP N RGD:5509061 20171005 MGI PMID:18252720 1315615 Enam enamelin gene MP:0030220 mandibular cyst IAGP N RGD:5509061 20171019 MGI PMID:24603688 1315615 Enam enamelin gene MP:0030221 maxillary cyst IAGP N RGD:5509061 20171019 MGI PMID:24603688 1315615 Enam enamelin gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20180125 MGI PMID:18252720 1315615 Enam enamelin gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20180125 MGI PMID:18252720 1315615 Enam enamelin gene MP:0030458 abnormal tooth wear IAGP N RGD:5509061 20180125 MGI PMID:18252720 1315615 Enam enamelin gene MP:0030459 abnormal tooth attrition IAGP N RGD:5509061 20180125 MGI PMID:18252720 1315615 Enam enamelin gene MP:0030514 absent Tomes' process IAGP N RGD:5509061 20180111 MGI PMID:24603688 1315619 Usp24 ubiquitin specific peptidase 24 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1315619 Usp24 ubiquitin specific peptidase 24 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20210617 MGI PMID:33355202 1315619 Usp24 ubiquitin specific peptidase 24 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20210617 MGI PMID:33355202 1315619 Usp24 ubiquitin specific peptidase 24 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1315619 Usp24 ubiquitin specific peptidase 24 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1315619 Usp24 ubiquitin specific peptidase 24 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20210617 MGI PMID:33355202 1315619 Usp24 ubiquitin specific peptidase 24 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20210617 MGI PMID:33355202 1315619 Usp24 ubiquitin specific peptidase 24 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20210617 MGI PMID:33355202 1315619 Usp24 ubiquitin specific peptidase 24 gene MP:0010343 increased lipoma incidence IAGP N RGD:5509061 20210617 MGI PMID:33355202 1315619 Usp24 ubiquitin specific peptidase 24 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20210617 MGI PMID:33355202 1315619 Usp24 ubiquitin specific peptidase 24 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20210617 MGI PMID:33355202 1315620 Rad51ap1 RAD51 associated protein 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1315620 Rad51ap1 RAD51 associated protein 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20240523 MGI 1315623 Naf1 nuclear assembly factor 1 ribonucleoprotein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170119 MGI PMID:27510903 1315623 Naf1 nuclear assembly factor 1 ribonucleoprotein gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20170119 MGI PMID:27510903 1315625 Mta3 metastasis associated 3 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 1315625 Mta3 metastasis associated 3 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1315625 Mta3 metastasis associated 3 gene MP:0001512 trunk curl IEA N RGD:5509061 20141003 MGI 1315625 Mta3 metastasis associated 3 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20160804 MGI 1315625 Mta3 metastasis associated 3 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1315625 Mta3 metastasis associated 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1315625 Mta3 metastasis associated 3 gene MP:0003062 abnormal coping response IEA N RGD:5509061 20160804 MGI 1315625 Mta3 metastasis associated 3 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1315625 Mta3 metastasis associated 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20160804 MGI 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:18213585 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150305 MGI PMID:22884328 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20150305 MGI PMID:22884328 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20150305 MGI PMID:22884328 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20150305 MGI PMID:22884328 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20150305 MGI PMID:22884328 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20150305 MGI PMID:22884328 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18213585 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:18213585 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18213585 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20150305 MGI PMID:22884328 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20150305 MGI PMID:22884328 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:18213585 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:18213585 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0009436 fragmentation of sleep/wake states IAGP N RGD:5509061 20150305 MGI PMID:22884328 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20150305 MGI PMID:22884328 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20150305 MGI PMID:24293317 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0012287 increased frequency of paradoxical sleep IAGP N RGD:5509061 20150305 MGI PMID:22884328 1315629 Mbnl2 muscleblind like splicing factor 2 gene MP:0012288 abnormal paradoxical sleep pattern IAGP N RGD:5509061 20150305 MGI PMID:22884328 1315631 Vpreb3 V-set pre-B cell surrogate light chain 3 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 1315633 Lsm4 LSM4 homolog, U6 small nuclear RNA and mRNA degradation associated gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10629062 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180301 MGI PMID:28923496 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0000603 pale liver IAGP N RGD:5509061 20180301 MGI PMID:28923496 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180301 MGI PMID:28923496 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20181227 MGI 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20180301 MGI PMID:28923496 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180301 MGI PMID:28923496 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20181227 MGI 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20181227 MGI 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180301 MGI PMID:28923496 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0003103 liver degeneration IAGP N RGD:5509061 20180301 MGI PMID:28923496 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180301 MGI PMID:28923496 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0003674 oxidative stress IAGP N RGD:5509061 20180301 MGI PMID:28923496 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20180301 MGI PMID:28923496 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20180301 MGI PMID:28923496 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180301 MGI PMID:28923496 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20180301 MGI PMID:28923496 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20180301 MGI PMID:28923496 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0030718 increased circulating lysine level IAGP N RGD:5509061 20180920 MGI PMID:28923496 1315634 Nadk2 NAD kinase 2, mitochondrial gene MP:0030721 increased lysine level IAGP N RGD:5509061 20180920 MGI PMID:28923496 1315637 Hepacam hepatocyte cell adhesion molecule gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20190425 MGI PMID:28695146 1315637 Hepacam hepatocyte cell adhesion molecule gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20150827 MGI PMID:24647135 1315637 Hepacam hepatocyte cell adhesion molecule gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20150827 MGI PMID:24647135 1315637 Hepacam hepatocyte cell adhesion molecule gene MP:0005238 increased brain size IAGP N RGD:5509061 20190425 MGI PMID:28695146 1315637 Hepacam hepatocyte cell adhesion molecule gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20150827 MGI PMID:24647135 1315637 Hepacam hepatocyte cell adhesion molecule gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20190425 MGI PMID:28695146 1315637 Hepacam hepatocyte cell adhesion molecule gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20150827 MGI PMID:24647135 1315637 Hepacam hepatocyte cell adhesion molecule gene MP:0011854 cerebral edema IAGP N RGD:5509061 20190425 MGI PMID:28695146 1315640 Acsm1 acyl-CoA synthetase medium-chain family member 1 gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20230601 MGI 1315640 Acsm1 acyl-CoA synthetase medium-chain family member 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1315640 Acsm1 acyl-CoA synthetase medium-chain family member 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20230601 MGI 1315640 Acsm1 acyl-CoA synthetase medium-chain family member 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20230601 MGI 1315644 Kif3b kinesin family member 3B gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:9865700 1315644 Kif3b kinesin family member 3B gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9865700 1315644 Kif3b kinesin family member 3B gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:9865700 1315644 Kif3b kinesin family member 3B gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:9865700 1315644 Kif3b kinesin family member 3B gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20220421 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9865700 1315644 Kif3b kinesin family member 3B gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9865700 1315644 Kif3b kinesin family member 3B gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9865700 1315644 Kif3b kinesin family member 3B gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:9865700 1315644 Kif3b kinesin family member 3B gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:9865700 1315644 Kif3b kinesin family member 3B gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1315644 Kif3b kinesin family member 3B gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1315644 Kif3b kinesin family member 3B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9865700 1315644 Kif3b kinesin family member 3B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315644 Kif3b kinesin family member 3B gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0012445 thin hippocampus stratum radiatum IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0012775 abnormal brain weight IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1315644 Kif3b kinesin family member 3B gene MP:0020512 abnormal dendritic mushroom spine morphology IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315644 Kif3b kinesin family member 3B gene MP:0020870 decreased thigmotaxis IAGP N RGD:5509061 20200528 MGI PMID:31746486 1315646 Fermt1 fermitin family member 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19057668 1315646 Fermt1 fermitin family member 1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:19057668 1315646 Fermt1 fermitin family member 1 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:19057668 1315646 Fermt1 fermitin family member 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:19057668 1315646 Fermt1 fermitin family member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19057668 1315646 Fermt1 fermitin family member 1 gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:19057668 1315646 Fermt1 fermitin family member 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:19057668 1315646 Fermt1 fermitin family member 1 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:19057668 1315646 Fermt1 fermitin family member 1 gene MP:0008055 increased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:19057668 1315646 Fermt1 fermitin family member 1 gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20141003 MGI PMID:19057668 1315646 Fermt1 fermitin family member 1 gene MP:0009485 distended ileum IAGP N RGD:5509061 20141003 MGI PMID:19057668 1315646 Fermt1 fermitin family member 1 gene MP:0009511 distended stomach IAGP N RGD:5509061 20141003 MGI PMID:19057668 1315646 Fermt1 fermitin family member 1 gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19057668 1315646 Fermt1 fermitin family member 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19057668 1315646 Fermt1 fermitin family member 1 gene MP:0030578 decreased keratinocyte adhesion IAGP N RGD:5509061 20180607 MGI PMID:19057668 1315646 Fermt1 fermitin family member 1 gene MP:0030584 skin atrophy IAGP N RGD:5509061 20180614 MGI PMID:19057668 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18218778 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:18218778 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20150521 MGI PMID:25574476 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20150521 MGI PMID:25574476 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:18218778 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20180809 MGI PMID:28175314 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0000751 myopathy IAGP N RGD:5509061 20180809 MGI PMID:28175314 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20180809 MGI PMID:28175314 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20150521 MGI PMID:25574476 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18218778 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20150521 MGI PMID:25574476 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20190221 MGI PMID:28175314 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20150521 MGI PMID:25574476 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18218778 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20150521 MGI PMID:25574476 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0003335 exocrine pancreatic insufficiency IAGP N RGD:5509061 20150521 MGI PMID:25574476 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20150521 MGI PMID:25574476 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20180809 MGI PMID:28175314 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0004248 abnormal epaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:18218778 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:18218778 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20150521 MGI PMID:25574476 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20150521 MGI PMID:25574476 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20190221 MGI PMID:28175314 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20180809 MGI PMID:28175314 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20180809 MGI PMID:28175314 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0009420 skeletal muscle endomysial fibrosis IAGP N RGD:5509061 20180809 MGI PMID:28175314 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18218778 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20150521 MGI PMID:25574476 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180809 MGI PMID:28175314 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:18218778 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:25574476 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0020309 increased creatine kinase activity IAGP N RGD:5509061 20180809 MGI PMID:28175314 1315650 Ptrh2 peptidyl-tRNA hydrolase 2 gene MP:0030798 joint contracture IAGP N RGD:5509061 20190221 MGI PMID:28175314 1315653 Myh14 myosin, heavy polypeptide 14 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20861308 1315653 Myh14 myosin, heavy polypeptide 14 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20861308 1315653 Myh14 myosin, heavy polypeptide 14 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20231214 MGI PMID:20861308 1315653 Myh14 myosin, heavy polypeptide 14 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20861308 1315653 Myh14 myosin, heavy polypeptide 14 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:20861308 1315653 Myh14 myosin, heavy polypeptide 14 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:20861308 1315653 Myh14 myosin, heavy polypeptide 14 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20231214 MGI PMID:20861308 1315653 Myh14 myosin, heavy polypeptide 14 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:20861308 1315653 Myh14 myosin, heavy polypeptide 14 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20861308 1315653 Myh14 myosin, heavy polypeptide 14 gene MP:0012431 increased lymphoma incidence IEA N RGD:5509061 20141003 MGI 1315653 Myh14 myosin, heavy polypeptide 14 gene MP:0020850 abnormal microtubule cytoskeleton morphology IAGP N RGD:5509061 20231214 MGI PMID:20861308 1315653 Myh14 myosin, heavy polypeptide 14 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20231214 MGI PMID:20861308 1315653 Myh14 myosin, heavy polypeptide 14 gene MP:0031611 decreased fetal cardiomyocyte number IAGP N RGD:5509061 20240321 MGI PMID:20861308 1315655 Carf calcium response factor gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:20519520 1315655 Carf calcium response factor gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20220519 MGI 1315655 Carf calcium response factor gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1315655 Carf calcium response factor gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:20519520 1315655 Carf calcium response factor gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:20519520 1315655 Carf calcium response factor gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20210128 MGI 1315655 Carf calcium response factor gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:20519520 1315657 Donson downstream neighbor of SON gene MP:0000433 microcephaly IAGP N RGD:5509061 20240104 MGI PMID:37590370 1315657 Donson downstream neighbor of SON gene MP:0000547 short limbs IAGP N RGD:5509061 20240104 MGI PMID:37590370 1315657 Donson downstream neighbor of SON gene MP:0001265 decreased body size IAGP N RGD:5509061 20240104 MGI PMID:37590370 1315657 Donson downstream neighbor of SON gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20240104 MGI PMID:37590370 1315657 Donson downstream neighbor of SON gene MP:0009850 embryonic lethality between implantation and placentation IAGP N RGD:5509061 20180524 MGI PMID:28630177 1315665 C1qc complement component 1, q subcomponent, C chain gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20230601 MGI 1315665 C1qc complement component 1, q subcomponent, C chain gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20210826 MGI 1315665 C1qc complement component 1, q subcomponent, C chain gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20210826 MGI 1315665 C1qc complement component 1, q subcomponent, C chain gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1315665 C1qc complement component 1, q subcomponent, C chain gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20240523 MGI 1315665 C1qc complement component 1, q subcomponent, C chain gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1315665 C1qc complement component 1, q subcomponent, C chain gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 1315665 C1qc complement component 1, q subcomponent, C chain gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1315667 Gpr33 G protein-coupled receptor 33 gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17965774 1315669 Stim1 stromal interaction molecule 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17965774 1315669 Stim1 stromal interaction molecule 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0000745 tremors IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0000751 myopathy IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0000754 paresis IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:21530328 1315669 Stim1 stromal interaction molecule 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0001304 cataract IEA N RGD:5509061 20210520 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:18559454 1315669 Stim1 stromal interaction molecule 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20220519 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18559454 1315669 Stim1 stromal interaction molecule 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17965774 1315669 Stim1 stromal interaction molecule 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:18059272 1315669 Stim1 stromal interaction molecule 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0002083 premature death IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20240509 MGI PMID:34359900 1315669 Stim1 stromal interaction molecule 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0002221 abnormal lymph organ size IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20201022 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:17965774 1315669 Stim1 stromal interaction molecule 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21530328 1315669 Stim1 stromal interaction molecule 1 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:18059272 1315669 Stim1 stromal interaction molecule 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20201022 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20240509 MGI PMID:34359900 1315669 Stim1 stromal interaction molecule 1 gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17965774 1315669 Stim1 stromal interaction molecule 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210128 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18559454 1315669 Stim1 stromal interaction molecule 1 gene MP:0004233 abnormal muscle weight IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0004510 myositis IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21530328 1315669 Stim1 stromal interaction molecule 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19843959 1315669 Stim1 stromal interaction molecule 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21530328 1315669 Stim1 stromal interaction molecule 1 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:17965774 1315669 Stim1 stromal interaction molecule 1 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:18559454 1315669 Stim1 stromal interaction molecule 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21530328 1315669 Stim1 stromal interaction molecule 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18059272 1315669 Stim1 stromal interaction molecule 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:17965774 1315669 Stim1 stromal interaction molecule 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21941299 1315669 Stim1 stromal interaction molecule 1 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:17965774 1315669 Stim1 stromal interaction molecule 1 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:18559454 1315669 Stim1 stromal interaction molecule 1 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21530328 1315669 Stim1 stromal interaction molecule 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21530328 1315669 Stim1 stromal interaction molecule 1 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17965774 1315669 Stim1 stromal interaction molecule 1 gene MP:0008407 decreased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:21746875 1315669 Stim1 stromal interaction molecule 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17965774 1315669 Stim1 stromal interaction molecule 1 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18059272 1315669 Stim1 stromal interaction molecule 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:21530328 1315669 Stim1 stromal interaction molecule 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:18059272 1315669 Stim1 stromal interaction molecule 1 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21530328 1315669 Stim1 stromal interaction molecule 1 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21530328 1315669 Stim1 stromal interaction molecule 1 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:18059272 1315669 Stim1 stromal interaction molecule 1 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:21530328 1315669 Stim1 stromal interaction molecule 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:18059272 1315669 Stim1 stromal interaction molecule 1 gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:18059272 1315669 Stim1 stromal interaction molecule 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0009420 skeletal muscle endomysial fibrosis IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0009422 decreased gastrocnemius weight IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0009422 decreased gastrocnemius weight IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0009425 increased soleus weight IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0009425 increased soleus weight IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:18559454 1315669 Stim1 stromal interaction molecule 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:18059272 1315669 Stim1 stromal interaction molecule 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0010089 abnormal circulating creatine kinase level IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20240509 MGI PMID:34359900 1315669 Stim1 stromal interaction molecule 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18559454 1315669 Stim1 stromal interaction molecule 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18059272 1315669 Stim1 stromal interaction molecule 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18327260 1315669 Stim1 stromal interaction molecule 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17965774 1315669 Stim1 stromal interaction molecule 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315669 Stim1 stromal interaction molecule 1 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17965774 1315669 Stim1 stromal interaction molecule 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0011585 decreased alkaline phosphatase activity IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20240509 MGI PMID:34359900 1315669 Stim1 stromal interaction molecule 1 gene MP:0011747 myelofibrosis IAGP N RGD:5509061 20141003 MGI PMID:17965774 1315669 Stim1 stromal interaction molecule 1 gene MP:0013022 increased Ly6C high monocyte number IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0013026 decreased Ly6C low monocyte number IAGP N RGD:5509061 20230420 MGI PMID:31666234 1315669 Stim1 stromal interaction molecule 1 gene MP:0013621 decreased internal diameter of femur IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0013639 decreased bone stiffness IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0014292 decreased internal diameter of tibia IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0014344 abnormal skeletal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315669 Stim1 stromal interaction molecule 1 gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:21530328 1315669 Stim1 stromal interaction molecule 1 gene MP:0020240 increased skeletal muscle cell apoptosis IAGP N RGD:5509061 20240509 MGI PMID:34359900 1315669 Stim1 stromal interaction molecule 1 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20240509 MGI PMID:34359900 1315669 Stim1 stromal interaction molecule 1 gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20240509 MGI PMID:34359900 1315669 Stim1 stromal interaction molecule 1 gene MP:0031402 decreased muscle fatigability IAGP N RGD:5509061 20240509 MGI PMID:30576443 1315673 Prima1 proline rich membrane anchor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19357277 1315673 Prima1 proline rich membrane anchor 1 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19357277 1315673 Prima1 proline rich membrane anchor 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19357277 1315675 Mcm3ap minichromosome maintenance complex component 3 associated protein gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:14715907 1315675 Mcm3ap minichromosome maintenance complex component 3 associated protein gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:14715907 1315675 Mcm3ap minichromosome maintenance complex component 3 associated protein gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:14715907 1315675 Mcm3ap minichromosome maintenance complex component 3 associated protein gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14715907 1315675 Mcm3ap minichromosome maintenance complex component 3 associated protein gene MP:0008093 abnormal memory B cell number IAGP N RGD:5509061 20141003 MGI PMID:14715907 1315675 Mcm3ap minichromosome maintenance complex component 3 associated protein gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:14715907 1315675 Mcm3ap minichromosome maintenance complex component 3 associated protein gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14715907 1315675 Mcm3ap minichromosome maintenance complex component 3 associated protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17903179 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220811 MGI 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0000274 enlarged heart IEA N RGD:5509061 20220811 MGI 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20181227 MGI 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0001326 retina degeneration IAGP N RGD:5509061 20150129 MGI PMID:21052544 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0001326 retina degeneration IAGP N RGD:5509061 20150129 MGI PMID:22183357 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:18849587 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210520 MGI 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220811 MGI 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:18849587 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20150129 MGI PMID:22183357 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18849587 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0008025 brain vacuoles IEA N RGD:5509061 20141003 MGI 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:18849587 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:18849587 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20150129 MGI PMID:22183357 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:18849587 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:18849587 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:18849587 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20141003 MGI PMID:18849587 1315677 Pde6a phosphodiesterase 6A, cGMP-specific, rod, alpha gene MP:0012671 retina spots IEA N RGD:5509061 20141003 MGI 1315682 Plgrkt plasminogen receptor, C-terminal lysine transmembrane protein gene MP:0001194 dermatitis IAGP N RGD:5509061 20200123 MGI PMID:27714956 1315682 Plgrkt plasminogen receptor, C-terminal lysine transmembrane protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200123 MGI PMID:27714956 1315682 Plgrkt plasminogen receptor, C-terminal lysine transmembrane protein gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200123 MGI PMID:27714956 1315682 Plgrkt plasminogen receptor, C-terminal lysine transmembrane protein gene MP:0003718 maternal effect IAGP N RGD:5509061 20200123 MGI PMID:27714956 1315682 Plgrkt plasminogen receptor, C-terminal lysine transmembrane protein gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20200123 MGI PMID:27714956 1315682 Plgrkt plasminogen receptor, C-terminal lysine transmembrane protein gene MP:0013716 hypolactation IAGP N RGD:5509061 20200123 MGI PMID:27714956 1315682 Plgrkt plasminogen receptor, C-terminal lysine transmembrane protein gene MP:0020212 impaired leukocyte migration IAGP N RGD:5509061 20200123 MGI PMID:27714956 1315685 Ints11 integrator complex subunit 11 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315687 Car7 carbonic anhydrase 7 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20210128 MGI 1315687 Car7 carbonic anhydrase 7 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220811 MGI 1315687 Car7 carbonic anhydrase 7 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:23881097 1315687 Car7 carbonic anhydrase 7 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1315687 Car7 carbonic anhydrase 7 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:23881097 1315690 Retreg2 reticulophagy regulator family member 2 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1315690 Retreg2 reticulophagy regulator family member 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200514 MGI 1315690 Retreg2 reticulophagy regulator family member 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200514 MGI 1315690 Retreg2 reticulophagy regulator family member 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200514 MGI 1315690 Retreg2 reticulophagy regulator family member 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1315690 Retreg2 reticulophagy regulator family member 2 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20240523 MGI 1315690 Retreg2 reticulophagy regulator family member 2 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1315692 Il18rap interleukin 18 receptor accessory protein gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20221215 MGI 1315692 Il18rap interleukin 18 receptor accessory protein gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1315692 Il18rap interleukin 18 receptor accessory protein gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20201022 MGI 1315692 Il18rap interleukin 18 receptor accessory protein gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15843532 1315692 Il18rap interleukin 18 receptor accessory protein gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15843532 1315692 Il18rap interleukin 18 receptor accessory protein gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20211021 MGI 1315692 Il18rap interleukin 18 receptor accessory protein gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20210826 MGI 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20231207 MGI 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:15009730 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20231207 MGI 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0001324 abnormal eye pigmentation IEA N RGD:5509061 20111116 MGI 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:15109702 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20231207 MGI 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20231207 MGI 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20231207 MGI 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20141003 MGI PMID:15109702 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0002963 decreased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:1912584 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:5367369 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0002980 abnormal postural reflex IEA N RGD:5509061 20111116 MGI 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0003173 decreased lysosomal enzyme secretion IAGP N RGD:5509061 20141003 MGI PMID:1912584 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0004721 abnormal platelet dense granule morphology IAGP N RGD:5509061 20141003 MGI PMID:1912584 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:1912584 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:1912584 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0004812 abnormal linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:15109702 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20141003 MGI PMID:1912584 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:15009730 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20160811 MGI PMID:11912185 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0005102 abnormal iris pigmentation IEA N RGD:5509061 20231207 MGI 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20160811 MGI PMID:11912185 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0005191 head tilt IEA N RGD:5509061 20111116 MGI 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:1912584 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20160811 MGI PMID:11912185 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:1912584 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:1912584 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20141003 MGI PMID:1912584 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20141003 MGI PMID:1912584 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:1912584 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20231207 MGI 1315694 Bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170720 MGI PMID:1912584 1315700 Xrcc3 X-ray repair complementing defective repair in Chinese hamster cells 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20220721 MGI PMID:34601382 1315700 Xrcc3 X-ray repair complementing defective repair in Chinese hamster cells 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20220721 MGI PMID:34601382 1315700 Xrcc3 X-ray repair complementing defective repair in Chinese hamster cells 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20220721 MGI PMID:34601382 1315700 Xrcc3 X-ray repair complementing defective repair in Chinese hamster cells 3 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1315700 Xrcc3 X-ray repair complementing defective repair in Chinese hamster cells 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20220721 MGI PMID:34601382 1315700 Xrcc3 X-ray repair complementing defective repair in Chinese hamster cells 3 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20220721 MGI PMID:34601382 1315700 Xrcc3 X-ray repair complementing defective repair in Chinese hamster cells 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20220721 MGI PMID:34601382 1315700 Xrcc3 X-ray repair complementing defective repair in Chinese hamster cells 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:10421844 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:14499111 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:10421844 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:12060722 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12060722 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000577 absent eccrine glands IAGP N RGD:5509061 20141003 MGI PMID:12060722 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:12060722 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12060722 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:14499111 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:14499111 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000819 abnormal olfactory bulb morphology IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0000914 exencephaly IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:12060722 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10421844 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10421844 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14499111 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10421844 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:18097000 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12060722 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0002199 abnormal brain commissure morphology IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0002219 decreased lymph node number IAGP N RGD:5509061 20141003 MGI PMID:10421844 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:14499111 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14499111 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0002717 abnormal male preputial gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12060722 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0003253 dilated bile duct IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0003262 intestinal/bowel diverticulum IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0003584 bifid ureter IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:14499111 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:12060722 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0003931 absent molars IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0004056 abnormal myocardium compact layer morphology IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0004666 absent stapedial artery IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0005004 abnormal lymphocyte anergy IAGP N RGD:5509061 20141003 MGI PMID:18097000 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0005046 absent spleen white pulp IAGP N RGD:5509061 20141003 MGI PMID:14499111 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18097000 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0005107 abnormal stapes morphology IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:18423196 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0006365 absent guard hair IAGP N RGD:5509061 20141003 MGI PMID:12060722 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18097000 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14499111 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:14499111 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10421844 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0008387 hypochromic anemia IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:10421844 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18423196 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:14499111 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:18097000 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:18097000 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:14499111 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0010572 persistent right dorsal aorta IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0010912 herniated liver IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10421844 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14499111 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10215628 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10421844 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0012303 umbilical vein stenosis IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0013382 small perianal sebaceous gland IAGP N RGD:5509061 20141218 MGI PMID:12060722 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0013385 abnormal Meibomian gland development IAGP N RGD:5509061 20141225 MGI PMID:12060722 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0013842 ductus venosus stenosis IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0013878 abnormal ductus venosus valve topology IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0013917 persistent right 6th pharyngeal arch artery IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0013918 abnormal endolymphatic sac topology IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0013968 multiple persisting craniopharyngeal ducts IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0013975 abnormal coronary sinus connection IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20170504 MGI 1315707 Traf6 TNF receptor-associated factor 6 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1315709 Mlf1 myeloid leukemia factor 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20190103 MGI PMID:26563351 1315709 Mlf1 myeloid leukemia factor 1 gene MP:0009341 decreased splenocyte apoptosis IAGP N RGD:5509061 20190103 MGI PMID:26563351 1315709 Mlf1 myeloid leukemia factor 1 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20190103 MGI PMID:26563351 1315713 Cdh7 cadherin 7, type 2 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1315718 Kin Kin17 DNA and RNA binding protein gene MP:0002626 increased heart rate IEA N RGD:5509061 20211021 MGI 1315718 Kin Kin17 DNA and RNA binding protein gene MP:0010507 shortened RR interval IEA N RGD:5509061 20220811 MGI 1315718 Kin Kin17 DNA and RNA binding protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1315718 Kin Kin17 DNA and RNA binding protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1315721 Ralgapb Ral GTPase activating protein, beta subunit (non-catalytic) gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20211021 MGI 1315721 Ralgapb Ral GTPase activating protein, beta subunit (non-catalytic) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315724 Cd34 CD34 antigen gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17483328 1315724 Cd34 CD34 antigen gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17483328 1315724 Cd34 CD34 antigen gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17483328 1315724 Cd34 CD34 antigen gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:17483328 1315724 Cd34 CD34 antigen gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:17483328 1315724 Cd34 CD34 antigen gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8555469 1315724 Cd34 CD34 antigen gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17483328 1315724 Cd34 CD34 antigen gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8611677 1315724 Cd34 CD34 antigen gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8555469 1315724 Cd34 CD34 antigen gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17483328 1315724 Cd34 CD34 antigen gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:8555469 1315724 Cd34 CD34 antigen gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:8555469 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:15755804 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9636176 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15755804 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9250866 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9636176 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0000926 absent floor plate IAGP N RGD:5509061 20180215 MGI PMID:28817564 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:9250866 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15755804 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:9250866 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0001288 abnormal lens induction IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:9250866 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:9636176 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9250866 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20180215 MGI PMID:28817564 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0002728 absent tibia IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:9250866 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:9250866 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:9250866 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0005226 abnormal vertebral arch development IAGP N RGD:5509061 20141003 MGI PMID:9250866 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:9250866 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0009688 abnormal spinal cord central canal morphology IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0009689 abnormal neural tube ventricular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7720556 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0009827 skin detachment IAGP N RGD:5509061 20170309 MGI PMID:9250866 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9636176 1315729 Rab23 RAB23, member RAS oncogene family gene MP:0012707 incomplete caudal neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:9636176 1315731 Brpf3 bromodomain and PHD finger containing, 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160804 MGI 1315731 Brpf3 bromodomain and PHD finger containing, 3 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20160804 MGI 1315733 Il36a interleukin 36A gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20201210 MGI PMID:29794016 1315733 Il36a interleukin 36A gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20201210 MGI PMID:29794016 1315736 Rhobtb1 Rho-related BTB domain containing 1 gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20200514 MGI 1315736 Rhobtb1 Rho-related BTB domain containing 1 gene MP:0005355 enlarged thyroid gland IEA N RGD:5509061 20200514 MGI 1315736 Rhobtb1 Rho-related BTB domain containing 1 gene MP:0013679 increased Ly6C-positive NK T cell number IEA N RGD:5509061 20210826 MGI 1315738 Dock5 dedicator of cytokinesis 5 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:9093026 1315738 Dock5 dedicator of cytokinesis 5 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315738 Dock5 dedicator of cytokinesis 5 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315738 Dock5 dedicator of cytokinesis 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18820033 1315739 Tecpr1 tectonin beta-propeller repeat containing 1 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:21575909 1315739 Tecpr1 tectonin beta-propeller repeat containing 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:21575909 1315748 Vps26c VPS26 endosomal protein sorting factor C gene MP:0000603 pale liver IEA N RGD:5509061 20210826 MGI 1315748 Vps26c VPS26 endosomal protein sorting factor C gene MP:0001284 absent vibrissae IEA N RGD:5509061 20220519 MGI 1315748 Vps26c VPS26 endosomal protein sorting factor C gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1315748 Vps26c VPS26 endosomal protein sorting factor C gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201022 MGI 1315748 Vps26c VPS26 endosomal protein sorting factor C gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20220519 MGI 1315748 Vps26c VPS26 endosomal protein sorting factor C gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20220519 MGI 1315748 Vps26c VPS26 endosomal protein sorting factor C gene MP:0002080 prenatal lethality IEA N RGD:5509061 20210826 MGI 1315748 Vps26c VPS26 endosomal protein sorting factor C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315749 Rimkla ribosomal modification protein rimK-like family member A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20230223 MGI PMID:33638175 1315749 Rimkla ribosomal modification protein rimK-like family member A gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:33638175 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20201022 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0001147 small testis IEA N RGD:5509061 20201022 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220407 MGI PMID:12950107 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10471512 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220407 MGI PMID:12950107 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0002188 small heart IEA N RGD:5509061 20201022 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210826 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20200514 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:10471512 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10471512 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10471512 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220407 MGI PMID:12950107 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200514 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20200514 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20200514 MGI 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10471512 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20220407 MGI PMID:12950107 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220407 MGI PMID:12950107 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:10471512 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220407 MGI PMID:12950107 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220407 MGI PMID:12950107 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:10471512 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0009231 detached acrosome IAGP N RGD:5509061 20141003 MGI PMID:10471512 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0009231 detached acrosome IAGP N RGD:5509061 20220407 MGI PMID:12950107 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:10471512 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:10471512 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220407 MGI PMID:12950107 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220407 MGI PMID:12950107 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220407 MGI PMID:10471512 1315752 Csnk2a2 casein kinase 2, alpha prime polypeptide gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1315753 Frrs1 ferric-chelate reductase 1 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20211021 MGI 1315753 Frrs1 ferric-chelate reductase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1315753 Frrs1 ferric-chelate reductase 1 gene MP:0011940 decreased food intake IEA N RGD:5509061 20211021 MGI 1315754 Grap GRB2-related adaptor protein gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11971956 1315754 Grap GRB2-related adaptor protein gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11971956 1315755 Fcrl2 Fc receptor like 2 gene MP:0001260 increased body weight IEA N RGD:5509061 20170406 MGI 1315755 Fcrl2 Fc receptor like 2 gene MP:0001264 increased body size IEA N RGD:5509061 20170406 MGI 1315755 Fcrl2 Fc receptor like 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20230601 MGI 1315755 Fcrl2 Fc receptor like 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20170406 MGI 1315755 Fcrl2 Fc receptor like 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 1315755 Fcrl2 Fc receptor like 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20170406 MGI 1315755 Fcrl2 Fc receptor like 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20170406 MGI 1315755 Fcrl2 Fc receptor like 2 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20230601 MGI 1315755 Fcrl2 Fc receptor like 2 gene MP:0012323 increased total tissue mass IEA N RGD:5509061 20170406 MGI 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16024820 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23135277 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:16024820 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23135277 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0003326 liver failure IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23135277 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0004264 abnormal extraembryonic tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23135277 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:23135277 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:23135277 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23135277 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16024820 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23135277 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0011897 decreased circulating unsaturated transferrin level IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210211 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0012356 increased prothrombin time IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0012359 increased partial thromboplastin time IAGP N RGD:5509061 20141003 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:21907140 1315758 Fbxl5 F-box and leucine-rich repeat protein 5 gene MP:0020369 increased intestinal iron level IAGP N RGD:5509061 20161020 MGI PMID:23135277 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11113182 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7774011 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:7774011 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:9716588 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7774011 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9558405 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7774011 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:11113182 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15060151 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7774011 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9716588 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:7774011 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:7774011 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:9558405 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:9716588 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0003714 absent platelets IAGP N RGD:5509061 20141003 MGI PMID:7774011 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:7774011 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:15005853 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:15005853 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7774011 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:7774011 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0009439 increased myeloid sarcoma incidence IAGP N RGD:5509061 20200813 MGI PMID:30755419 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11113182 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:15005853 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0010961 increased compact bone mass IAGP N RGD:5509061 20141003 MGI PMID:15005853 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7774011 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7774011 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:15005853 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0020399 enhanced megakaryocyte emperipolesis IAGP N RGD:5509061 20170803 MGI PMID:7774011 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0020838 increased acute myeloid leukemia incidence IAGP N RGD:5509061 20200813 MGI PMID:30755419 1315760 Nfe2 nuclear factor, erythroid derived 2 gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:11113182 1315764 Prox1 prospero homeobox 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20170831 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170831 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170831 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20170831 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:10888866 1315764 Prox1 prospero homeobox 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:10888866 1315764 Prox1 prospero homeobox 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20170831 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:22791897 1315764 Prox1 prospero homeobox 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:12692551 1315764 Prox1 prospero homeobox 1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:10080188 1315764 Prox1 prospero homeobox 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:12692551 1315764 Prox1 prospero homeobox 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:10499794 1315764 Prox1 prospero homeobox 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20360386 1315764 Prox1 prospero homeobox 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20170831 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20360386 1315764 Prox1 prospero homeobox 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20170831 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17908929 1315764 Prox1 prospero homeobox 1 gene MP:0002450 abnormal lymph organ development IAGP N RGD:5509061 20141003 MGI PMID:10499794 1315764 Prox1 prospero homeobox 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20170831 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170831 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20141003 MGI PMID:10499794 1315764 Prox1 prospero homeobox 1 gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0003660 chylothorax IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:10888866 1315764 Prox1 prospero homeobox 1 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:16122728 1315764 Prox1 prospero homeobox 1 gene MP:0004937 dilated heart IAGP N RGD:5509061 20170831 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:10080188 1315764 Prox1 prospero homeobox 1 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0008107 absent retina horizontal cells IAGP N RGD:5509061 20141003 MGI PMID:12692551 1315764 Prox1 prospero homeobox 1 gene MP:0008269 abnormal hippocampus CA4 region morphology IAGP N RGD:5509061 20141003 MGI PMID:22791897 1315764 Prox1 prospero homeobox 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:20360386 1315764 Prox1 prospero homeobox 1 gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0009159 increased pancreatic acinar cell number IAGP N RGD:5509061 20141003 MGI PMID:16122728 1315764 Prox1 prospero homeobox 1 gene MP:0009165 abnormal endocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:16122728 1315764 Prox1 prospero homeobox 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22791897 1315764 Prox1 prospero homeobox 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0010194 absent lymphatic vessels IAGP N RGD:5509061 20141003 MGI PMID:17908929 1315764 Prox1 prospero homeobox 1 gene MP:0010198 decreased lymphatic vessel endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:20360386 1315764 Prox1 prospero homeobox 1 gene MP:0010416 interventricular septum membranous part aneurysm IAGP N RGD:5509061 20170831 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0010498 abnormal interventricular septum muscular part morphology IAGP N RGD:5509061 20170831 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0010626 thick tricuspid valve cusps IAGP N RGD:5509061 20170831 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10080188 1315764 Prox1 prospero homeobox 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10080188 1315764 Prox1 prospero homeobox 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16170315 1315764 Prox1 prospero homeobox 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170831 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10080188 1315764 Prox1 prospero homeobox 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10499794 1315764 Prox1 prospero homeobox 1 gene MP:0011964 increased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:12692551 1315764 Prox1 prospero homeobox 1 gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20170831 MGI PMID:24938781 1315764 Prox1 prospero homeobox 1 gene MP:0031147 abnormal ventricular thrombosis IAGP N RGD:5509061 20201210 MGI PMID:24938781 1315766 Rbm4 RNA binding motif protein 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23129807 1315766 Rbm4 RNA binding motif protein 4 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:23129807 1315766 Rbm4 RNA binding motif protein 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23129807 1315766 Rbm4 RNA binding motif protein 4 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23129807 1315766 Rbm4 RNA binding motif protein 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23129807 1315766 Rbm4 RNA binding motif protein 4 gene MP:0008497 decreased IgG2b level IEA N RGD:5509061 20160804 MGI 1315766 Rbm4 RNA binding motif protein 4 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:23129807 1315766 Rbm4 RNA binding motif protein 4 gene MP:0010147 abnormal endocrine pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:23129807 1315768 Zfp580 zinc finger protein 580 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1315768 Zfp580 zinc finger protein 580 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1315768 Zfp580 zinc finger protein 580 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1315769 Spns3 SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative) gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20190502 MGI 1315769 Spns3 SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative) gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 1315769 Spns3 SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative) gene MP:0003068 enlarged kidney IEA N RGD:5509061 20190502 MGI 1315769 Spns3 SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative) gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1315769 Spns3 SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative) gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1315769 Spns3 SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative) gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20190502 MGI 1315772 Fmnl2 formin-like 2 gene MP:0002764 short tibia IEA N RGD:5509061 20210520 MGI 1315772 Fmnl2 formin-like 2 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20211021 MGI 1315772 Fmnl2 formin-like 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1315773 Igtp interferon gamma induced GTPase gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:10639151 1315773 Igtp interferon gamma induced GTPase gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15908352 1315773 Igtp interferon gamma induced GTPase gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20211118 MGI PMID:34078740 1315773 Igtp interferon gamma induced GTPase gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:10639151 1315773 Igtp interferon gamma induced GTPase gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:10639151 1315775 Edc3 enhancer of mRNA decapping 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20190502 MGI 1315775 Edc3 enhancer of mRNA decapping 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20190502 MGI 1315775 Edc3 enhancer of mRNA decapping 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20190502 MGI 1315775 Edc3 enhancer of mRNA decapping 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20190502 MGI 1315775 Edc3 enhancer of mRNA decapping 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20190502 MGI 1315775 Edc3 enhancer of mRNA decapping 3 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1315775 Edc3 enhancer of mRNA decapping 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20201022 MGI 1315775 Edc3 enhancer of mRNA decapping 3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20190502 MGI 1315775 Edc3 enhancer of mRNA decapping 3 gene MP:0003604 single kidney IEA N RGD:5509061 20190502 MGI 1315775 Edc3 enhancer of mRNA decapping 3 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20190502 MGI 1315778 Atp6v0d2 ATPase, H+ transporting, lysosomal V0 subunit D2 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:17128270 1315778 Atp6v0d2 ATPase, H+ transporting, lysosomal V0 subunit D2 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:17128270 1315778 Atp6v0d2 ATPase, H+ transporting, lysosomal V0 subunit D2 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:17128270 1315778 Atp6v0d2 ATPase, H+ transporting, lysosomal V0 subunit D2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:17128270 1315778 Atp6v0d2 ATPase, H+ transporting, lysosomal V0 subunit D2 gene MP:0031073 decreased circulating type I collagen C-terminal telopeptide level IAGP N RGD:5509061 20200618 MGI PMID:17128270 1315781 Psmd7 proteasome (prosome, macropain) 26S subunit, non-ATPase, 7 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2824282 1315793 Fitm1 fat storage-inducing transmembrane protein 1 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20210429 MGI PMID:30923760 1315793 Fitm1 fat storage-inducing transmembrane protein 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1315793 Fitm1 fat storage-inducing transmembrane protein 1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210429 MGI PMID:30923760 1315793 Fitm1 fat storage-inducing transmembrane protein 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1315795 Kyat1 kynurenine aminotransferase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1315795 Kyat1 kynurenine aminotransferase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1315795 Kyat1 kynurenine aminotransferase 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1315797 Pex19 peroxisomal biogenesis factor 19 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1315797 Pex19 peroxisomal biogenesis factor 19 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1315797 Pex19 peroxisomal biogenesis factor 19 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 1315797 Pex19 peroxisomal biogenesis factor 19 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0000679 increased percent water in carcass IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0003441 increased glycerol level IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20160414 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0010358 abnormal free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21969596 1315799 Lgals12 lectin, galactose binding, soluble 12 gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:21969596 1315802 Lmtk2 lemur tyrosine kinase 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1315802 Lmtk2 lemur tyrosine kinase 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1315802 Lmtk2 lemur tyrosine kinase 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1315802 Lmtk2 lemur tyrosine kinase 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17158803 1315802 Lmtk2 lemur tyrosine kinase 2 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17158803 1315802 Lmtk2 lemur tyrosine kinase 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 1315802 Lmtk2 lemur tyrosine kinase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17158803 1315802 Lmtk2 lemur tyrosine kinase 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1315802 Lmtk2 lemur tyrosine kinase 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1315802 Lmtk2 lemur tyrosine kinase 2 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1315802 Lmtk2 lemur tyrosine kinase 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:17158803 1315802 Lmtk2 lemur tyrosine kinase 2 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1315802 Lmtk2 lemur tyrosine kinase 2 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1315802 Lmtk2 lemur tyrosine kinase 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17158803 1315808 Sumo1 small ubiquitin-like modifier 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1315808 Sumo1 small ubiquitin-like modifier 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1315808 Sumo1 small ubiquitin-like modifier 1 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20231207 MGI 1315808 Sumo1 small ubiquitin-like modifier 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18573887 1315808 Sumo1 small ubiquitin-like modifier 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19033381 1315808 Sumo1 small ubiquitin-like modifier 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23213215 1315808 Sumo1 small ubiquitin-like modifier 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151112 MGI PMID:24891386 1315808 Sumo1 small ubiquitin-like modifier 1 gene MP:0008799 oblique facial cleft IAGP N RGD:5509061 20141003 MGI PMID:16990542 1315808 Sumo1 small ubiquitin-like modifier 1 gene MP:0008886 abnormal PML bodies IAGP N RGD:5509061 20141003 MGI PMID:19033381 1315808 Sumo1 small ubiquitin-like modifier 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16990542 1315808 Sumo1 small ubiquitin-like modifier 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16990542 1315808 Sumo1 small ubiquitin-like modifier 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16990542 1315808 Sumo1 small ubiquitin-like modifier 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1315810 Jade1 jade family PHD finger 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1315810 Jade1 jade family PHD finger 1 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1315810 Jade1 jade family PHD finger 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14612400 1315813 Aebp1 AE binding protein 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20190502 MGI 1315813 Aebp1 AE binding protein 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20190502 MGI 1315813 Aebp1 AE binding protein 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11438679 1315813 Aebp1 AE binding protein 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:11438679 1315813 Aebp1 AE binding protein 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:11438679 1315813 Aebp1 AE binding protein 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11438679 1315813 Aebp1 AE binding protein 1 gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:11438679 1315813 Aebp1 AE binding protein 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:11438679 1315813 Aebp1 AE binding protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17299101 1315813 Aebp1 AE binding protein 1 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:17299101 1315813 Aebp1 AE binding protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 1315813 Aebp1 AE binding protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17299101 1315813 Aebp1 AE binding protein 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17299101 1315813 Aebp1 AE binding protein 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:11438679 1315813 Aebp1 AE binding protein 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20221103 MGI 1315813 Aebp1 AE binding protein 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17299101 1315813 Aebp1 AE binding protein 1 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17299101 1315813 Aebp1 AE binding protein 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:11438679 1315813 Aebp1 AE binding protein 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17299101 1315813 Aebp1 AE binding protein 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17299101 1315813 Aebp1 AE binding protein 1 gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:17299101 1315813 Aebp1 AE binding protein 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:11438679 1315813 Aebp1 AE binding protein 1 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17299101 1315813 Aebp1 AE binding protein 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17299101 1315813 Aebp1 AE binding protein 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11438679 1315813 Aebp1 AE binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315813 Aebp1 AE binding protein 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17299101 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20220901 MGI PMID:31209365 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0000433 microcephaly IAGP N RGD:5509061 20220901 MGI PMID:31209365 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20240523 MGI 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20191128 MGI 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20220901 MGI PMID:31209365 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20220901 MGI PMID:31209365 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20220901 MGI PMID:31209365 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20220901 MGI PMID:31209365 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20220901 MGI PMID:31209365 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20220901 MGI PMID:31209365 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20220901 MGI PMID:31209365 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20220901 MGI PMID:31209365 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20220901 MGI PMID:31209365 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1315816 Tubgcp4 tubulin, gamma complex component 4 gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20220901 MGI PMID:31209365 1315817 Trappc2b trafficking protein particle complex 2B gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20230720 MGI 1315817 Trappc2b trafficking protein particle complex 2B gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1315817 Trappc2b trafficking protein particle complex 2B gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20230720 MGI 1315822 Dusp18 dual specificity phosphatase 18 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1315822 Dusp18 dual specificity phosphatase 18 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1315822 Dusp18 dual specificity phosphatase 18 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1315822 Dusp18 dual specificity phosphatase 18 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20240523 MGI 1315822 Dusp18 dual specificity phosphatase 18 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1315824 Dynlrb2 dynein light chain roadblock-type 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1315824 Dynlrb2 dynein light chain roadblock-type 2 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1315824 Dynlrb2 dynein light chain roadblock-type 2 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1315824 Dynlrb2 dynein light chain roadblock-type 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20160114 MGI 1315824 Dynlrb2 dynein light chain roadblock-type 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20170105 MGI 1315824 Dynlrb2 dynein light chain roadblock-type 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1315824 Dynlrb2 dynein light chain roadblock-type 2 gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20160114 MGI 1315824 Dynlrb2 dynein light chain roadblock-type 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1315824 Dynlrb2 dynein light chain roadblock-type 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315826 Slc30a5 solute carrier family 30 (zinc transporter), member 5 gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20141003 MGI PMID:12095919 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:23849778 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:23849778 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0000650 mesocardia IEA N RGD:5509061 20141003 MGI 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0000692 small spleen IEA N RGD:5509061 20220519 MGI 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20141003 MGI 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23849778 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0001925 male infertility IEA N RGD:5509061 20220519 MGI 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0001943 abnormal respiration IEA N RGD:5509061 20141003 MGI 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23849778 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:23849778 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0004880 lung cyst IEA N RGD:5509061 20141003 MGI 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23849778 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0005330 cardiomyopathy IEA N RGD:5509061 20141003 MGI 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141003 MGI 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23849778 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23849778 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0010808 right-sided stomach IEA N RGD:5509061 20141003 MGI 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:23849778 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:23849778 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0011250 abdominal situs ambiguus IAGP N RGD:5509061 20141003 MGI PMID:23849778 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0011252 situs inversus totalis IAGP N RGD:5509061 20141003 MGI PMID:23849778 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0011649 immotile respiratory cilia IAGP N RGD:5509061 20141003 MGI PMID:23849778 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0011666 double outlet right ventricle, ventricular defect committed to aorta IEA N RGD:5509061 20141003 MGI 1315829 Odad2 outer dynein arm docking complex subunit 2 gene MP:0011683 dual inferior vena cava IAGP N RGD:5509061 20141003 MGI PMID:23849778 1315831 Bcl9 B cell CLL/lymphoma 9 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:19699733 1315831 Bcl9 B cell CLL/lymphoma 9 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20231207 MGI 1315831 Bcl9 B cell CLL/lymphoma 9 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1315831 Bcl9 B cell CLL/lymphoma 9 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20231207 MGI 1315831 Bcl9 B cell CLL/lymphoma 9 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:19699733 1315831 Bcl9 B cell CLL/lymphoma 9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1315831 Bcl9 B cell CLL/lymphoma 9 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1315831 Bcl9 B cell CLL/lymphoma 9 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:19699733 1315837 Cpxm1 carboxypeptidase X, M14 family member 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20221215 MGI 1315837 Cpxm1 carboxypeptidase X, M14 family member 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1315837 Cpxm1 carboxypeptidase X, M14 family member 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20220519 MGI 1315837 Cpxm1 carboxypeptidase X, M14 family member 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:11207276 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11207276 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:21750041 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21750041 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:11207276 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21750041 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17072340 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:11207276 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11207276 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:21750041 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21750041 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21750041 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11207276 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:11207276 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:11207276 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11207276 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:11207276 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11207276 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:21750041 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9109487 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:21750041 1315841 Mybl1 myeloblastosis oncogene-like 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:9109487 1315847 Rad51d RAD51 paralog D gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10705376 1315847 Rad51d RAD51 paralog D gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:10705376 1315847 Rad51d RAD51 paralog D gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:10705376 1315847 Rad51d RAD51 paralog D gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10705376 1315847 Rad51d RAD51 paralog D gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:10705376 1315847 Rad51d RAD51 paralog D gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10705376 1315847 Rad51d RAD51 paralog D gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:10705376 1315847 Rad51d RAD51 paralog D gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:10705376 1315847 Rad51d RAD51 paralog D gene MP:0008405 decreased cellular sensitivity to methylmethanesulfonate IAGP N RGD:5509061 20141003 MGI PMID:10705376 1315847 Rad51d RAD51 paralog D gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10705376 1315854 Insm2 insulinoma-associated 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20230406 MGI PMID:30359270 1315854 Insm2 insulinoma-associated 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20230406 MGI PMID:30359270 1315854 Insm2 insulinoma-associated 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20230406 MGI PMID:30359270 1315854 Insm2 insulinoma-associated 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20230406 MGI PMID:30359270 1315854 Insm2 insulinoma-associated 2 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20230406 MGI PMID:30359270 1315854 Insm2 insulinoma-associated 2 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20230406 MGI PMID:30359270 1315864 Gkap1 G kinase anchoring protein 1 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20201119 MGI PMID:31318116 1315864 Gkap1 G kinase anchoring protein 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210520 MGI 1315864 Gkap1 G kinase anchoring protein 1 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20201119 MGI PMID:31318116 1315864 Gkap1 G kinase anchoring protein 1 gene MP:0004928 increased epididymis weight IAGP N RGD:5509061 20201119 MGI PMID:31318116 1315864 Gkap1 G kinase anchoring protein 1 gene MP:0004931 enlarged epididymis IAGP N RGD:5509061 20201119 MGI PMID:31318116 1315864 Gkap1 G kinase anchoring protein 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20201119 MGI PMID:31318116 1315864 Gkap1 G kinase anchoring protein 1 gene MP:0009256 enlarged corpus epididymis IAGP N RGD:5509061 20201119 MGI PMID:31318116 1315864 Gkap1 G kinase anchoring protein 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1315864 Gkap1 G kinase anchoring protein 1 gene MP:0030603 increased sperm number IAGP N RGD:5509061 20201119 MGI PMID:31318116 1315866 Ovol1 ovo like zinc finger 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1315866 Ovol1 ovo like zinc finger 1 gene MP:0000398 splitting of guard hairs IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0000405 abnormal auchene hair morphology IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0001123 dilated uterus IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0001136 dilated uterine cervix IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0001143 constricted vagina orifice IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201231 MGI 1315866 Ovol1 ovo like zinc finger 1 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20160421 MGI 1315866 Ovol1 ovo like zinc finger 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:17049212 1315866 Ovol1 ovo like zinc finger 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1315866 Ovol1 ovo like zinc finger 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1315866 Ovol1 ovo like zinc finger 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1315866 Ovol1 ovo like zinc finger 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17049212 1315866 Ovol1 ovo like zinc finger 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:9808631 1315866 Ovol1 ovo like zinc finger 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17049212 1315866 Ovol1 ovo like zinc finger 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17049212 1315870 Ppp2r3a protein phosphatase 2, regulatory subunit B'', alpha gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1315870 Ppp2r3a protein phosphatase 2, regulatory subunit B'', alpha gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14736746 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22020280 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23706823 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:22020280 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:14736746 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23706823 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:14736746 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22020280 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23706823 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:23706823 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23706823 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:14736746 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:22020280 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22020280 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23706823 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:22020280 1315878 Piwil2 piwi-like RNA-mediated gene silencing 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:14736746 1315880 Cln5 ceroid-lipofuscinosis, neuronal 5 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:15459177 1315880 Cln5 ceroid-lipofuscinosis, neuronal 5 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15459177 1315880 Cln5 ceroid-lipofuscinosis, neuronal 5 gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20141003 MGI PMID:15459177 1315885 Suv39h2 suppressor of variegation 3-9 2 gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:11701123 1315885 Suv39h2 suppressor of variegation 3-9 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11701123 1315885 Suv39h2 suppressor of variegation 3-9 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11701123 1315885 Suv39h2 suppressor of variegation 3-9 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:11701123 1315885 Suv39h2 suppressor of variegation 3-9 2 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11701123 1315885 Suv39h2 suppressor of variegation 3-9 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:11701123 1315885 Suv39h2 suppressor of variegation 3-9 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11701123 1315892 Rtp4 receptor transporter protein 4 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20231207 MGI 1315892 Rtp4 receptor transporter protein 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1315892 Rtp4 receptor transporter protein 4 gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20201112 MGI PMID:32709745 1315892 Rtp4 receptor transporter protein 4 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20240523 MGI 1315892 Rtp4 receptor transporter protein 4 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20201112 MGI PMID:32709745 1315892 Rtp4 receptor transporter protein 4 gene MP:0010751 decreased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20201112 MGI PMID:32709745 1315892 Rtp4 receptor transporter protein 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220519 MGI 1315894 Btbd9 BTB domain containing 9 gene MP:0000860 abnormal primary somatosensory cortex morphology IAGP N RGD:5509061 20210107 MGI PMID:31715135 1315894 Btbd9 BTB domain containing 9 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20210107 MGI PMID:32446853 1315894 Btbd9 BTB domain containing 9 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1315894 Btbd9 BTB domain containing 9 gene MP:0001396 unidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:22678064 1315894 Btbd9 BTB domain containing 9 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20210107 MGI PMID:31715135 1315894 Btbd9 BTB domain containing 9 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210107 MGI PMID:31715135 1315894 Btbd9 BTB domain containing 9 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:22678064 1315894 Btbd9 BTB domain containing 9 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20170105 MGI 1315894 Btbd9 BTB domain containing 9 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20210107 MGI PMID:31715135 1315894 Btbd9 BTB domain containing 9 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20210107 MGI PMID:32446853 1315894 Btbd9 BTB domain containing 9 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20210107 MGI PMID:31715135 1315894 Btbd9 BTB domain containing 9 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22536397 1315894 Btbd9 BTB domain containing 9 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20210107 MGI PMID:31715135 1315894 Btbd9 BTB domain containing 9 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20210107 MGI PMID:32446853 1315894 Btbd9 BTB domain containing 9 gene MP:0003663 abnormal thermosensation IAGP N RGD:5509061 20141003 MGI PMID:22678064 1315894 Btbd9 BTB domain containing 9 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22536397 1315894 Btbd9 BTB domain containing 9 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:22536397 1315894 Btbd9 BTB domain containing 9 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20210107 MGI PMID:31715135 1315894 Btbd9 BTB domain containing 9 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20170105 MGI 1315894 Btbd9 BTB domain containing 9 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:22678064 1315894 Btbd9 BTB domain containing 9 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:22678064 1315894 Btbd9 BTB domain containing 9 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22536397 1315894 Btbd9 BTB domain containing 9 gene MP:0009455 enhanced cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22536397 1315894 Btbd9 BTB domain containing 9 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1315894 Btbd9 BTB domain containing 9 gene MP:0011396 abnormal sleep behavior IAGP N RGD:5509061 20210107 MGI PMID:31715135 1315894 Btbd9 BTB domain containing 9 gene MP:0011396 abnormal sleep behavior IAGP N RGD:5509061 20210107 MGI PMID:32446853 1315894 Btbd9 BTB domain containing 9 gene MP:0012448 abnormal primary motor cortex morphology IAGP N RGD:5509061 20210107 MGI PMID:31715135 1315894 Btbd9 BTB domain containing 9 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1315894 Btbd9 BTB domain containing 9 gene MP:0014254 increased paired-pulse ratio IAGP N RGD:5509061 20230706 MGI PMID:22536397 1315894 Btbd9 BTB domain containing 9 gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:32446853 1315894 Btbd9 BTB domain containing 9 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22678064 1315894 Btbd9 BTB domain containing 9 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:32446853 1315897 Ptov1 prostate tumor over expressed gene 1 gene MP:0000111 cleft palate IEA N RGD:5509061 20221215 MGI 1315897 Ptov1 prostate tumor over expressed gene 1 gene MP:0000562 polydactyly IEA N RGD:5509061 20221215 MGI 1315897 Ptov1 prostate tumor over expressed gene 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1315897 Ptov1 prostate tumor over expressed gene 1 gene MP:0001785 edema IEA N RGD:5509061 20221215 MGI 1315897 Ptov1 prostate tumor over expressed gene 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20221215 MGI 1315897 Ptov1 prostate tumor over expressed gene 1 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20221215 MGI 1315897 Ptov1 prostate tumor over expressed gene 1 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20221215 MGI 1315897 Ptov1 prostate tumor over expressed gene 1 gene MP:0008797 facial cleft IEA N RGD:5509061 20221215 MGI 1315897 Ptov1 prostate tumor over expressed gene 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1315899 C1qtnf7 C1q and tumor necrosis factor related protein 7 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20180315 MGI PMID:28223291 1315899 C1qtnf7 C1q and tumor necrosis factor related protein 7 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180315 MGI PMID:28223291 1315899 C1qtnf7 C1q and tumor necrosis factor related protein 7 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180315 MGI PMID:28223291 1315899 C1qtnf7 C1q and tumor necrosis factor related protein 7 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20180315 MGI PMID:28223291 1315899 C1qtnf7 C1q and tumor necrosis factor related protein 7 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180315 MGI PMID:28223291 1315901 Ankrd60 ankyrin repeat domain 60 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20240523 MGI 1315901 Ankrd60 ankyrin repeat domain 60 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20240523 MGI 1315901 Ankrd60 ankyrin repeat domain 60 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1315903 Piwil1 piwi-like RNA-mediated gene silencing 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22121019 1315903 Piwil1 piwi-like RNA-mediated gene silencing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12062093 1315903 Piwil1 piwi-like RNA-mediated gene silencing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22121019 1315903 Piwil1 piwi-like RNA-mediated gene silencing 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12062093 1315903 Piwil1 piwi-like RNA-mediated gene silencing 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:22121019 1315903 Piwil1 piwi-like RNA-mediated gene silencing 1 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12062093 1315903 Piwil1 piwi-like RNA-mediated gene silencing 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:22121019 1315903 Piwil1 piwi-like RNA-mediated gene silencing 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12062093 1315903 Piwil1 piwi-like RNA-mediated gene silencing 1 gene MP:0031620 abnormal chromatoid body morphology IAGP N RGD:5509061 20240613 MGI PMID:22121019 1315907 Cfl2 cofilin 2, muscle gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315907 Cfl2 cofilin 2, muscle gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22343409 1315908 Tmem165 transmembrane protein 165 gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20160804 MGI 1315908 Tmem165 transmembrane protein 165 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1315910 Btn1a1 butyrophilin, subfamily 1, member A1 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:15226505 1315910 Btn1a1 butyrophilin, subfamily 1, member A1 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:15226505 1315910 Btn1a1 butyrophilin, subfamily 1, member A1 gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:15226505 1315912 Bcl2l13 BCL2 like 13 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240229 MGI PMID:36608143 1315913 Ttc29 tetratricopeptide repeat domain 29 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:31735294 1315913 Ttc29 tetratricopeptide repeat domain 29 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220714 MGI PMID:31735294 1315913 Ttc29 tetratricopeptide repeat domain 29 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20200310 MGI PMID:31735294 1315913 Ttc29 tetratricopeptide repeat domain 29 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20200310 MGI PMID:31735294 1315913 Ttc29 tetratricopeptide repeat domain 29 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20200310 MGI PMID:31735294 1315913 Ttc29 tetratricopeptide repeat domain 29 gene MP:0009837 abnormal sperm end piece morphology IAGP N RGD:5509061 20200310 MGI PMID:31735294 1315913 Ttc29 tetratricopeptide repeat domain 29 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20230601 MGI 1315913 Ttc29 tetratricopeptide repeat domain 29 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20200310 MGI PMID:31735294 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0000599 enlarged liver IEA N RGD:5509061 20210520 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210520 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210520 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20201022 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15175329 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:15175329 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:23254996 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1315917 Chst2 carbohydrate sulfotransferase 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9197240 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16682947 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22701168 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9197240 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:15280420 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:8275084 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9197240 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15280420 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:12466203 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12466203 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:9197240 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0001203 increased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:16682947 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22701168 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22701168 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9197240 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:9197240 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12466203 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12466203 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:12466203 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11713303 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22701168 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9197240 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12466203 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11713303 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:9197240 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0003031 acidosis IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:8275084 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:8275084 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0003325 decreased liver function IAGP N RGD:5509061 20141003 MGI PMID:8275084 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:11713303 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9197240 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20141003 MGI PMID:11713303 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:8275084 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:11713303 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:8275084 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20200206 MGI PMID:22257940 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:16682947 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20200206 MGI PMID:22257940 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22701168 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:15280420 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15280420 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20200206 MGI PMID:22257940 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12466203 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200206 MGI PMID:22257940 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22701168 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:9197240 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9197240 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22701168 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20200206 MGI PMID:22257940 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:16682947 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:8275084 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9197240 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15280420 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8275084 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16682947 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17183314 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9197240 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0011126 absent primary ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:12466203 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200206 MGI PMID:22257940 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:11713303 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20150409 MGI PMID:22701168 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0013705 decreased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20150409 MGI PMID:22701168 1315922 Ercc1 excision repair cross-complementing rodent repair deficiency, complementation group 1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20200206 MGI PMID:22257940 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20160804 MGI 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:19068231 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20160804 MGI 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:19068231 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0002074 abnormal hair texture IEA N RGD:5509061 20160804 MGI 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0002608 increased hematocrit IEA N RGD:5509061 20160804 MGI 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19068231 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:19068231 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:19068231 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20160922 MGI PMID:24652767 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1315924 Rad18 RAD18 E3 ubiquitin protein ligase gene MP:0010679 abnormal arrector pilli muscle morphology IAGP N RGD:5509061 20190124 MGI PMID:25340873 1315928 Psme3 proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki) gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10608895 1315928 Psme3 proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10608895 1315928 Psme3 proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15004203 1315928 Psme3 proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki) gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:15004203 1315928 Psme3 proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki) gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:15004203 1315928 Psme3 proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki) gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:15004203 1315928 Psme3 proteaseome (prosome, macropain) activator subunit 3 (PA28 gamma, Ki) gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:15004203 1315931 Thsd1 thrombospondin, type I, domain 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160421 MGI 1315931 Thsd1 thrombospondin, type I, domain 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20170105 MGI 1315933 Gpx7 glutathione peroxidase 7 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0001333 absent optic nerve IEA N RGD:5509061 20181227 MGI 1315933 Gpx7 glutathione peroxidase 7 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1315933 Gpx7 glutathione peroxidase 7 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20221215 MGI 1315933 Gpx7 glutathione peroxidase 7 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1315933 Gpx7 glutathione peroxidase 7 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0010318 increased salivary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0010799 stomach mucosa hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1315933 Gpx7 glutathione peroxidase 7 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23123197 1315933 Gpx7 glutathione peroxidase 7 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:23123197 1315947 Dcun1d5 defective in cullin neddylation 1 domain containing 5 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210826 MGI 1315947 Dcun1d5 defective in cullin neddylation 1 domain containing 5 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20221215 MGI 1315947 Dcun1d5 defective in cullin neddylation 1 domain containing 5 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20221215 MGI 1315951 Fxr2 FMR1 autosomal homolog 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11875043 1315951 Fxr2 FMR1 autosomal homolog 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11875043 1315951 Fxr2 FMR1 autosomal homolog 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11875043 1315951 Fxr2 FMR1 autosomal homolog 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11875043 1315951 Fxr2 FMR1 autosomal homolog 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:11875043 1315951 Fxr2 FMR1 autosomal homolog 2 gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:11875043 1315951 Fxr2 FMR1 autosomal homolog 2 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:11875043 1315951 Fxr2 FMR1 autosomal homolog 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1315951 Fxr2 FMR1 autosomal homolog 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:11875043 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000071 axial skeleton hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23479625 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:6119797 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:1269836 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:23479625 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:7202842 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:6151297 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:6151297 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:23479625 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:67117 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:23479625 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000588 thick tail IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20230601 MGI 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:624676 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:67117 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:1269836 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:15882565 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:6151297 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:67117 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:858816 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9671738 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:67117 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:6151297 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:67117 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:858816 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20230601 MGI 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:23479625 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0004340 short scapula IAGP N RGD:5509061 20141003 MGI PMID:23479625 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:23479625 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:23479625 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:23479625 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:23479625 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:23479625 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:9671738 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:8835524 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:67117 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:23479625 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:858816 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:6151297 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:5713631 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:858816 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0009908 protruding tongue IEA N RGD:5509061 20230601 MGI 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23479625 1315953 Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1315957 Mob1a MOB kinase activator 1A gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315957 Mob1a MOB kinase activator 1A gene MP:0000611 jaundice IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315957 Mob1a MOB kinase activator 1A gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0001257 increased body length IEA N RGD:5509061 20230119 MGI 1315957 Mob1a MOB kinase activator 1A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0002083 premature death IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315957 Mob1a MOB kinase activator 1A gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0002981 increased liver weight IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315957 Mob1a MOB kinase activator 1A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0003158 dysphagia IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20230601 MGI 1315957 Mob1a MOB kinase activator 1A gene MP:0003252 abnormal bile duct physiology IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315957 Mob1a MOB kinase activator 1A gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315957 Mob1a MOB kinase activator 1A gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315957 Mob1a MOB kinase activator 1A gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315957 Mob1a MOB kinase activator 1A gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0003769 abnormal lip morphology IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315957 Mob1a MOB kinase activator 1A gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315957 Mob1a MOB kinase activator 1A gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0009581 decreased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0009877 exostosis IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0010293 increased integument system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0010297 increased hepatobiliary system tumor incidence IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315957 Mob1a MOB kinase activator 1A gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315957 Mob1a MOB kinase activator 1A gene MP:0010318 increased salivary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315957 Mob1a MOB kinase activator 1A gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0011686 increased epidermal stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:23143302 1315957 Mob1a MOB kinase activator 1A gene MP:0012236 abnormal cholangiocyte morphology IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315957 Mob1a MOB kinase activator 1A gene MP:0013119 abdomen swellings IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315957 Mob1a MOB kinase activator 1A gene MP:0014038 increased hepatocyte number IAGP N RGD:5509061 20170601 MGI PMID:26699479 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20231207 MGI 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0000380 small hair follicles IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0000392 accelerated hair follicle regression IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0000674 abnormal sweat gland morphology IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0000763 abnormal filiform papillae morphology IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0001258 decreased body length IEA N RGD:5509061 20230601 MGI 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20231207 MGI 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20170119 MGI PMID:25629078 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0002992 abnormal sebaceous lipid secretion IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0003931 absent molars IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0003932 abnormal molar crown morphology IAGP N RGD:5509061 20170119 MGI PMID:25629078 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20170119 MGI PMID:25629078 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0006257 abnormal fungiform papillae morphology IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0006260 abnormal gustatory papilla taste bud morphology IAGP N RGD:5509061 20230601 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0006402 small molars IAGP N RGD:5509061 20170119 MGI PMID:25629078 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0006402 small molars IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20231207 MGI 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0010773 supernumerary molars IAGP N RGD:5509061 20170119 MGI PMID:25629078 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0010773 supernumerary molars IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0011194 abnormal hair follicle physiology IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0013371 hypohidrosis IAGP N RGD:5509061 20170810 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0030451 abnormal dentin mineralization IAGP N RGD:5509061 20180215 MGI PMID:25629078 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20171228 MGI PMID:25629078 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20180125 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0030491 dental pulp stones IAGP N RGD:5509061 20171228 MGI PMID:25629078 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0030494 abnormal molar root morphology IAGP N RGD:5509061 20180125 MGI PMID:28589954 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0030496 taurodontia IAGP N RGD:5509061 20171228 MGI PMID:25629078 1315959 Wnt10a wingless-type MMTV integration site family, member 10A gene MP:0030524 abnormal tooth root resorption IAGP N RGD:5509061 20180118 MGI PMID:25629078 1315961 Plscr3 phospholipid scramblase 3 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15328404 1315961 Plscr3 phospholipid scramblase 3 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15328404 1315961 Plscr3 phospholipid scramblase 3 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15328404 1315961 Plscr3 phospholipid scramblase 3 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15328404 1315961 Plscr3 phospholipid scramblase 3 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20190815 MGI PMID:15328404 1315961 Plscr3 phospholipid scramblase 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15328404 1315961 Plscr3 phospholipid scramblase 3 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15328404 1315961 Plscr3 phospholipid scramblase 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15328404 1315961 Plscr3 phospholipid scramblase 3 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15328404 1315961 Plscr3 phospholipid scramblase 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15328404 1315961 Plscr3 phospholipid scramblase 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15328404 1315961 Plscr3 phospholipid scramblase 3 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15328404 1315961 Plscr3 phospholipid scramblase 3 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:15328404 1315961 Plscr3 phospholipid scramblase 3 gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:15328404 1315964 Niban2 niban apoptosis regulator 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1315968 Poldip2 polymerase (DNA-directed), delta interacting protein 2 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23825363 1315968 Poldip2 polymerase (DNA-directed), delta interacting protein 2 gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:23825363 1315968 Poldip2 polymerase (DNA-directed), delta interacting protein 2 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:23825363 1315968 Poldip2 polymerase (DNA-directed), delta interacting protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23825363 1315968 Poldip2 polymerase (DNA-directed), delta interacting protein 2 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:23825363 1315968 Poldip2 polymerase (DNA-directed), delta interacting protein 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:23825363 1315968 Poldip2 polymerase (DNA-directed), delta interacting protein 2 gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:23825363 1315968 Poldip2 polymerase (DNA-directed), delta interacting protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23825363 1315968 Poldip2 polymerase (DNA-directed), delta interacting protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20220106 MGI PMID:34928942 1315970 Rhot1 ras homolog family member T1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20170817 MGI PMID:27705781 1315970 Rhot1 ras homolog family member T1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0001391 abnormal tail movements IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20170817 MGI PMID:27705781 1315970 Rhot1 ras homolog family member T1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0002083 premature death IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20170817 MGI PMID:27705781 1315970 Rhot1 ras homolog family member T1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20170817 MGI PMID:27705781 1315970 Rhot1 ras homolog family member T1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20170817 MGI PMID:27705781 1315970 Rhot1 ras homolog family member T1 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20170817 MGI PMID:27705781 1315970 Rhot1 ras homolog family member T1 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20170817 MGI PMID:27705781 1315970 Rhot1 ras homolog family member T1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20170817 MGI PMID:27705781 1315970 Rhot1 ras homolog family member T1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20170817 MGI PMID:27705781 1315970 Rhot1 ras homolog family member T1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20170817 MGI PMID:27705781 1315970 Rhot1 ras homolog family member T1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20170817 MGI PMID:27705781 1315970 Rhot1 ras homolog family member T1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170817 MGI PMID:27705781 1315970 Rhot1 ras homolog family member T1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315970 Rhot1 ras homolog family member T1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20170817 MGI PMID:27705781 1315970 Rhot1 ras homolog family member T1 gene MP:0012051 spasticity IAGP N RGD:5509061 20150402 MGI PMID:25136135 1315970 Rhot1 ras homolog family member T1 gene MP:0014345 abnormal neuron mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:27705781 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20161201 MGI 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20161201 MGI 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9806640 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9806640 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9806640 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9806640 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:9806640 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0002491 decreased IgD level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:9806640 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0002533 abnormal type III hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:9806640 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210128 MGI 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:9806640 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20161201 MGI 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9806640 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0005265 abnormal blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9806640 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:11371362 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:11371362 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:11371362 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0008185 decreased naive B cell number IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:12574333 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:9806640 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:9806640 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9806640 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9806640 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9806640 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0012361 decreased large unstained cell number IEA N RGD:5509061 20161201 MGI 1315972 Ikzf3 IKAROS family zinc finger 3 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:12574333 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20170223 MGI PMID:22374166 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20170223 MGI PMID:22374166 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0003968 abnormal growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20170223 MGI PMID:22374166 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20170223 MGI PMID:22374166 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0011924 abnormal liver zinc level IAGP N RGD:5509061 20170223 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0011924 abnormal liver zinc level IAGP N RGD:5509061 20170223 MGI PMID:22374166 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20170223 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20170223 MGI PMID:21445361 1315976 Slc39a14 solute carrier family 39 (zinc transporter), member 14 gene MP:0030126 torticollis IAGP N RGD:5509061 20171005 MGI PMID:21445361 1315980 Gfus GDP-L-fucose synthase gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315980 Gfus GDP-L-fucose synthase gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12186857 1315984 Strn4 striatin, calmodulin binding protein 4 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230119 MGI 1315984 Strn4 striatin, calmodulin binding protein 4 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230119 MGI 1315984 Strn4 striatin, calmodulin binding protein 4 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210826 MGI 1315984 Strn4 striatin, calmodulin binding protein 4 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230119 MGI 1315984 Strn4 striatin, calmodulin binding protein 4 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1315984 Strn4 striatin, calmodulin binding protein 4 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1315984 Strn4 striatin, calmodulin binding protein 4 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230119 MGI 1315984 Strn4 striatin, calmodulin binding protein 4 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20230119 MGI 1315984 Strn4 striatin, calmodulin binding protein 4 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230119 MGI 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20231207 MGI 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0001177 atelectasis IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:20106877 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:12904583 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:20106877 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0001958 emphysema IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19884661 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0002952 ventricular cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20106877 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0003305 proctitis IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0004882 enlarged lung IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:12904583 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0009310 increased large intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19884661 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0010052 increased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19884661 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19884661 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12904583 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:20106877 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20240704 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12208849 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20150709 MGI PMID:25713297 1315989 Ltbp4 latent transforming growth factor beta binding protein 4 gene MP:0021159 increased heart right ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:25713297 1315990 Fry FRY microtubule binding protein gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 1315990 Fry FRY microtubule binding protein gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 1315990 Fry FRY microtubule binding protein gene MP:0004692 small pubis IAGP N RGD:5509061 20210930 MGI PMID:33905568 1315992 Cadm3 cell adhesion molecule 3 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:19036974 1315993 Lypd8 LY6/PLAUR domain containing 8 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20210415 MGI PMID:27027293 1315993 Lypd8 LY6/PLAUR domain containing 8 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20210415 MGI PMID:27027293 1315993 Lypd8 LY6/PLAUR domain containing 8 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20210415 MGI PMID:27027293 1315993 Lypd8 LY6/PLAUR domain containing 8 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170323 MGI 1315993 Lypd8 LY6/PLAUR domain containing 8 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20210415 MGI PMID:27027293 1315993 Lypd8 LY6/PLAUR domain containing 8 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20210415 MGI PMID:27027293 1315993 Lypd8 LY6/PLAUR domain containing 8 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20210415 MGI PMID:27027293 1315993 Lypd8 LY6/PLAUR domain containing 8 gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20210415 MGI PMID:27027293 1315995 Tmc5 transmembrane channel-like gene family 5 gene MP:0001925 male infertility IEA N RGD:5509061 20220811 MGI 1315997 Dusp11 dual specificity phosphatase 11 (RNA/RNP complex 1-interacting) gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201231 MGI 1315997 Dusp11 dual specificity phosphatase 11 (RNA/RNP complex 1-interacting) gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 1315997 Dusp11 dual specificity phosphatase 11 (RNA/RNP complex 1-interacting) gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1315997 Dusp11 dual specificity phosphatase 11 (RNA/RNP complex 1-interacting) gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20210617 MGI PMID:32796023 1315997 Dusp11 dual specificity phosphatase 11 (RNA/RNP complex 1-interacting) gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20210617 MGI PMID:32796023 1315997 Dusp11 dual specificity phosphatase 11 (RNA/RNP complex 1-interacting) gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20210617 MGI PMID:32796023 1315997 Dusp11 dual specificity phosphatase 11 (RNA/RNP complex 1-interacting) gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20210617 MGI PMID:32796023 1315997 Dusp11 dual specificity phosphatase 11 (RNA/RNP complex 1-interacting) gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210617 MGI PMID:32796023 1315997 Dusp11 dual specificity phosphatase 11 (RNA/RNP complex 1-interacting) gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20211021 MGI 1315997 Dusp11 dual specificity phosphatase 11 (RNA/RNP complex 1-interacting) gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20210617 MGI PMID:32796023 1315997 Dusp11 dual specificity phosphatase 11 (RNA/RNP complex 1-interacting) gene MP:0011078 increased macrophage cytokine production IAGP N RGD:5509061 20210617 MGI PMID:32796023 1315997 Dusp11 dual specificity phosphatase 11 (RNA/RNP complex 1-interacting) gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20160421 MGI 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18974875 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20230928 MGI PMID:35604347 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20230928 MGI PMID:35604347 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20230928 MGI PMID:35604347 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230928 MGI PMID:35604347 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:18974875 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:18974875 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:18974875 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:18974875 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18974875 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0001705 abnormal proximal-distal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18974875 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20230928 MGI PMID:35604347 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20220721 MGI PMID:28319097 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20230928 MGI PMID:35604347 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20191107 MGI PMID:30224759 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20230928 MGI PMID:35604347 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20190502 MGI 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0004609 vertebral fusion IEA N RGD:5509061 20201231 MGI 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20230928 MGI PMID:35604347 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20230928 MGI PMID:35604347 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:18974875 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20211014 MGI PMID:25417106 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0008918 microgliosis IAGP N RGD:5509061 20230928 MGI PMID:35604347 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0009593 absent chorion IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20220721 MGI PMID:28319097 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20211014 MGI PMID:25417106 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18974875 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0011190 thick embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20230928 MGI PMID:35604347 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20230928 MGI PMID:35604347 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0012159 absent anterior visceral endoderm IAGP N RGD:5509061 20141003 MGI PMID:18974875 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0012161 absent distal visceral endoderm IAGP N RGD:5509061 20141003 MGI PMID:18974875 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:18794365 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0012734 abnormal response to radiation IAGP N RGD:5509061 20191107 MGI PMID:30224759 1315999 Bptf bromodomain PHD finger transcription factor gene MP:0013893 decreased common lymphocyte progenitor cell number IAGP N RGD:5509061 20220721 MGI PMID:28319097 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:9618507 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:9876179 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:9618507 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:9618507 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17875933 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:17875933 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:17875933 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17875933 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17875933 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17875933 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17875933 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17875933 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17875933 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:17875933 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9876179 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17875933 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17875933 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22114267 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:22114267 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:9618507 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9618507 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9618507 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:17875933 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:22114267 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17875933 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17875933 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9618507 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9096336 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9876179 1316001 Map2k4 mitogen-activated protein kinase kinase 4 gene MP:0012235 abnormal liver bud morphology IAGP N RGD:5509061 20141003 MGI PMID:9618507 1316002 Pcid2 PCI domain containing 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0002227 abnormal spleen capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:20870947 1316002 Pcid2 PCI domain containing 2 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:20870947 1316002 Pcid2 PCI domain containing 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:20870947 1316002 Pcid2 PCI domain containing 2 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20870947 1316002 Pcid2 PCI domain containing 2 gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18339895 1316002 Pcid2 PCI domain containing 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200220 MGI PMID:24167073 1316002 Pcid2 PCI domain containing 2 gene MP:0014078 small intestinal villus atrophy IAGP N RGD:5509061 20160414 MGI PMID:18339895 1316014 Helz helicase with zinc finger domain gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10471385 1316014 Helz helicase with zinc finger domain gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1316016 Steap2 six transmembrane epithelial antigen of prostate 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1316016 Steap2 six transmembrane epithelial antigen of prostate 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1316020 Pus7 pseudouridylate synthase 7 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20220811 MGI 1316020 Pus7 pseudouridylate synthase 7 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1316020 Pus7 pseudouridylate synthase 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1316023 Fhl5 four and a half LIM domains 5 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15247423 1316023 Fhl5 four and a half LIM domains 5 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15247423 1316023 Fhl5 four and a half LIM domains 5 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:15247423 1316023 Fhl5 four and a half LIM domains 5 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:15247423 1316023 Fhl5 four and a half LIM domains 5 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15247423 1316023 Fhl5 four and a half LIM domains 5 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15247423 1316023 Fhl5 four and a half LIM domains 5 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15247423 1316023 Fhl5 four and a half LIM domains 5 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:15247423 1316023 Fhl5 four and a half LIM domains 5 gene MP:0008975 delayed male fertility IAGP N RGD:5509061 20141003 MGI PMID:15247423 1316023 Fhl5 four and a half LIM domains 5 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:15247423 1316023 Fhl5 four and a half LIM domains 5 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20141003 MGI PMID:15247423 1316023 Fhl5 four and a half LIM domains 5 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15247423 1316023 Fhl5 four and a half LIM domains 5 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:15247423 1316025 C1qtnf6 C1q and tumor necrosis factor related protein 6 gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20191031 MGI PMID:26404464 1316025 C1qtnf6 C1q and tumor necrosis factor related protein 6 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20191031 MGI PMID:26404464 1316025 C1qtnf6 C1q and tumor necrosis factor related protein 6 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20191031 MGI PMID:26404464 1316025 C1qtnf6 C1q and tumor necrosis factor related protein 6 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20191031 MGI PMID:26404464 1316025 C1qtnf6 C1q and tumor necrosis factor related protein 6 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20191031 MGI PMID:26404464 1316025 C1qtnf6 C1q and tumor necrosis factor related protein 6 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20191031 MGI PMID:26404464 1316025 C1qtnf6 C1q and tumor necrosis factor related protein 6 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20191031 MGI PMID:26404464 1316025 C1qtnf6 C1q and tumor necrosis factor related protein 6 gene MP:0005615 increased susceptibility to type III hypersensitivity reaction IAGP N RGD:5509061 20191031 MGI PMID:26404464 1316025 C1qtnf6 C1q and tumor necrosis factor related protein 6 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20191031 MGI PMID:26404464 1316025 C1qtnf6 C1q and tumor necrosis factor related protein 6 gene MP:0011566 abnormal complement protein level IAGP N RGD:5509061 20191031 MGI PMID:26404464 1316025 C1qtnf6 C1q and tumor necrosis factor related protein 6 gene MP:0020217 increased circulating complement protein level IAGP N RGD:5509061 20191031 MGI PMID:26404464 1316027 C1qtnf12 C1q and tumor necrosis factor related 12 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1316027 C1qtnf12 C1q and tumor necrosis factor related 12 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210128 MGI 1316027 C1qtnf12 C1q and tumor necrosis factor related 12 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1316027 C1qtnf12 C1q and tumor necrosis factor related 12 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 1316027 C1qtnf12 C1q and tumor necrosis factor related 12 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 1316029 Arhgef28 Rho guanine nucleotide exchange factor 28 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151112 MGI PMID:22649559 1316029 Arhgef28 Rho guanine nucleotide exchange factor 28 gene MP:0002865 increased growth rate IAGP N RGD:5509061 20151112 MGI PMID:22649559 1316029 Arhgef28 Rho guanine nucleotide exchange factor 28 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1316029 Arhgef28 Rho guanine nucleotide exchange factor 28 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20151112 MGI PMID:22649559 1316029 Arhgef28 Rho guanine nucleotide exchange factor 28 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20151112 MGI PMID:22649559 1316031 Rhog ras homolog family member G gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:14701744 1316031 Rhog ras homolog family member G gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14701744 1316031 Rhog ras homolog family member G gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14701744 1316031 Rhog ras homolog family member G gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14701744 1316031 Rhog ras homolog family member G gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:14701744 1316040 Snta1 syntrophin, acidic 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:10995443 1316040 Snta1 syntrophin, acidic 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:15548643 1316040 Snta1 syntrophin, acidic 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15548643 1316040 Snta1 syntrophin, acidic 1 gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:12578959 1316040 Snta1 syntrophin, acidic 1 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12578959 1316040 Snta1 syntrophin, acidic 1 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10995443 1316040 Snta1 syntrophin, acidic 1 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:15548643 1316040 Snta1 syntrophin, acidic 1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:12578959 1316042 Abca8b ATP-binding cassette, sub-family A member 8b gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20190411 MGI PMID:28882873 1316042 Abca8b ATP-binding cassette, sub-family A member 8b gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20190411 MGI PMID:28882873 1316042 Abca8b ATP-binding cassette, sub-family A member 8b gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20190411 MGI PMID:28882873 1316042 Abca8b ATP-binding cassette, sub-family A member 8b gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20190411 MGI PMID:28882873 1316050 Cog8 component of oligomeric golgi complex 8 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1316050 Cog8 component of oligomeric golgi complex 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1316050 Cog8 component of oligomeric golgi complex 8 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 1316052 Elp3 elongator acetyltransferase complex subunit 3 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20170608 MGI PMID:26527802 1316052 Elp3 elongator acetyltransferase complex subunit 3 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20170608 MGI PMID:26527802 1316052 Elp3 elongator acetyltransferase complex subunit 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20170427 MGI PMID:27476491 1316052 Elp3 elongator acetyltransferase complex subunit 3 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20170608 MGI PMID:26527802 1316052 Elp3 elongator acetyltransferase complex subunit 3 gene MP:0010156 abnormal small intestinal crypt cell physiology IAGP N RGD:5509061 20170608 MGI PMID:26527802 1316052 Elp3 elongator acetyltransferase complex subunit 3 gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20170608 MGI PMID:26527802 1316052 Elp3 elongator acetyltransferase complex subunit 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20170427 MGI PMID:27476491 1316052 Elp3 elongator acetyltransferase complex subunit 3 gene MP:0014353 abnormal gastrointestinal brush cell morphology IAGP N RGD:5509061 20240104 MGI PMID:26527802 1316052 Elp3 elongator acetyltransferase complex subunit 3 gene MP:0031319 impaired intestine regeneration IAGP N RGD:5509061 20211125 MGI PMID:26527802 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12963709 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0003462 abnormal response to novel odor IAGP N RGD:5509061 20160310 MGI PMID:26647347 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0014115 cognitive inflexibility IAGP N RGD:5509061 20160317 MGI PMID:26647347 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0020340 abnormal inhibitory learning IAGP N RGD:5509061 20160915 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:21962519 1316053 Cntnap2 contactin associated protein-like 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:26647347 1316055 Rybp RING1 and YY1 binding protein gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16055728 1316055 Rybp RING1 and YY1 binding protein gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20141003 MGI PMID:17470285 1316055 Rybp RING1 and YY1 binding protein gene MP:0001329 retina hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17470285 1316055 Rybp RING1 and YY1 binding protein gene MP:0001714 absent trophoblast giant cells IAGP N RGD:5509061 20141003 MGI PMID:16055728 1316055 Rybp RING1 and YY1 binding protein gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:16055728 1316055 Rybp RING1 and YY1 binding protein gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:16055728 1316055 Rybp RING1 and YY1 binding protein gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:16055728 1316055 Rybp RING1 and YY1 binding protein gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:16055728 1316055 Rybp RING1 and YY1 binding protein gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:16055728 1316055 Rybp RING1 and YY1 binding protein gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16055728 1316055 Rybp RING1 and YY1 binding protein gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:17470285 1316055 Rybp RING1 and YY1 binding protein gene MP:0010706 ventral rotation of lens IAGP N RGD:5509061 20141003 MGI PMID:17470285 1316055 Rybp RING1 and YY1 binding protein gene MP:0010715 retina coloboma IAGP N RGD:5509061 20141003 MGI PMID:17470285 1316055 Rybp RING1 and YY1 binding protein gene MP:0010717 optic nerve coloboma IAGP N RGD:5509061 20141003 MGI PMID:17470285 1316055 Rybp RING1 and YY1 binding protein gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16055728 1316055 Rybp RING1 and YY1 binding protein gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16055728 1316055 Rybp RING1 and YY1 binding protein gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16055728 1316055 Rybp RING1 and YY1 binding protein gene MP:0011193 embryonic epiblast cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16055728 1316055 Rybp RING1 and YY1 binding protein gene MP:0012102 absent trophectoderm IAGP N RGD:5509061 20141003 MGI PMID:16055728 1316059 Slc4a1ap solute carrier family 4 (anion exchanger), member 1, adaptor protein gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1316059 Slc4a1ap solute carrier family 4 (anion exchanger), member 1, adaptor protein gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20210128 MGI 1316061 Pan3 PAN3 poly(A) specific ribonuclease subunit gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210128 MGI 1316061 Pan3 PAN3 poly(A) specific ribonuclease subunit gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1316061 Pan3 PAN3 poly(A) specific ribonuclease subunit gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1316061 Pan3 PAN3 poly(A) specific ribonuclease subunit gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1316061 Pan3 PAN3 poly(A) specific ribonuclease subunit gene MP:0009476 enlarged cecum IEA N RGD:5509061 20210128 MGI 1316061 Pan3 PAN3 poly(A) specific ribonuclease subunit gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1316063 Trp73 transformation related protein 73 gene MP:0000344 absent Cajal-Retzius cell IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0000487 absent enterocytes IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0000503 excessive digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20194434 1316063 Trp73 transformation related protein 73 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:19805388 1316063 Trp73 transformation related protein 73 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:22160706 1316063 Trp73 transformation related protein 73 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:22160706 1316063 Trp73 transformation related protein 73 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:19805388 1316063 Trp73 transformation related protein 73 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:19805388 1316063 Trp73 transformation related protein 73 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:19805388 1316063 Trp73 transformation related protein 73 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0001355 submission towards male mice IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0001788 periorbital edema IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0001867 rhinitis IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0001872 sinus inflammation IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0001893 non-obstructive hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0001911 abnormal cerebrospinal fluid production IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:19805388 1316063 Trp73 transformation related protein 73 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:20194434 1316063 Trp73 transformation related protein 73 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:20194434 1316063 Trp73 transformation related protein 73 gene MP:0002243 abnormal vomeronasal organ morphology IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0002243 abnormal vomeronasal organ morphology IAGP N RGD:5509061 20141003 MGI PMID:19805388 1316063 Trp73 transformation related protein 73 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22160706 1316063 Trp73 transformation related protein 73 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19805388 1316063 Trp73 transformation related protein 73 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:20194434 1316063 Trp73 transformation related protein 73 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:19805388 1316063 Trp73 transformation related protein 73 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0004684 intervertebral disk degeneration IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20211021 MGI 1316063 Trp73 transformation related protein 73 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20210826 MGI 1316063 Trp73 transformation related protein 73 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20211021 MGI 1316063 Trp73 transformation related protein 73 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1316063 Trp73 transformation related protein 73 gene MP:0008031 decreased Cajal-Retzius cell number IAGP N RGD:5509061 20141003 MGI PMID:19805388 1316063 Trp73 transformation related protein 73 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22160706 1316063 Trp73 transformation related protein 73 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:22160706 1316063 Trp73 transformation related protein 73 gene MP:0008780 increased pancreatic acinar cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20194434 1316063 Trp73 transformation related protein 73 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:20194434 1316063 Trp73 transformation related protein 73 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:20194434 1316063 Trp73 transformation related protein 73 gene MP:0009485 distended ileum IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20194434 1316063 Trp73 transformation related protein 73 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20194434 1316063 Trp73 transformation related protein 73 gene MP:0009648 abnormal superovulation IAGP N RGD:5509061 20220804 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22160706 1316063 Trp73 transformation related protein 73 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10716451 1316063 Trp73 transformation related protein 73 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20194434 1316063 Trp73 transformation related protein 73 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1316063 Trp73 transformation related protein 73 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0013537 increased salivary gland adenoma incidence IAGP N RGD:5509061 20150219 MGI PMID:15837625 1316063 Trp73 transformation related protein 73 gene MP:0014445 abnormal spindle assembly in female meiosis IAGP N RGD:5509061 20240509 MGI PMID:18805989 1316063 Trp73 transformation related protein 73 gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220804 MGI PMID:18805989 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191205 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191205 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191205 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20220519 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20211021 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191205 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210128 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191205 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0012724 absent head fold IEA N RGD:5509061 20191205 MGI 1316065 Ska2 spindle and kinetochore associated complex subunit 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20160804 MGI 1316067 Tm9sf1 transmembrane 9 superfamily member 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:11050392 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:11050392 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11050391 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11050392 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:11050392 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20151217 MGI PMID:11260255 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:11050392 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20215524 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20215524 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20215524 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11050392 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11050393 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11260255 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11884603 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11050392 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20215524 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:11050392 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11050392 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:11884603 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:19204108 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11050392 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11050392 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:19204108 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:22547703 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:19204108 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22547703 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19204108 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22547703 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20220811 MGI 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:11050392 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:19204108 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19204108 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20215524 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11050393 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11050391 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11050392 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11260255 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11884603 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0012509 neural tube degeneration IAGP N RGD:5509061 20141003 MGI PMID:11050392 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0012556 increased cell death IAGP N RGD:5509061 20141003 MGI PMID:11050392 1316070 Rev3l REV3 like, DNA directed polymerase zeta catalytic subunit gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20151217 MGI PMID:11260255 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20200514 MGI 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20240328 MGI PMID:31220454 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0003036 vertebral transformation IEA N RGD:5509061 20201231 MGI 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20240328 MGI PMID:31220454 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20240328 MGI PMID:31220454 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0004165 abnormal lateral geniculate nucleus morphology IAGP N RGD:5509061 20240328 MGI PMID:31220454 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20200514 MGI 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20210520 MGI 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20240328 MGI PMID:31220454 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20240523 MGI 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:18952058 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20240328 MGI PMID:34208876 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20240328 MGI PMID:27615440 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20240328 MGI PMID:31220454 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0013771 decreased effector memory T-helper cell number IEA N RGD:5509061 20211021 MGI 1316072 Hcar1 hydrocarboxylic acid receptor 1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20240328 MGI PMID:31220454 1316074 Ntng2 netrin G2 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17973922 1316074 Ntng2 netrin G2 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:17973922 1316076 Sbf1 SET binding factor 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0000601 small liver IEA N RGD:5509061 20221215 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0000774 decreased brain size IEA N RGD:5509061 20210826 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11994405 1316076 Sbf1 SET binding factor 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11994405 1316076 Sbf1 SET binding factor 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220811 MGI PMID:34718573 1316076 Sbf1 SET binding factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220811 MGI PMID:34718573 1316076 Sbf1 SET binding factor 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20220811 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11994405 1316076 Sbf1 SET binding factor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220811 MGI PMID:34718573 1316076 Sbf1 SET binding factor 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220811 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210826 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0002175 decreased brain weight IEA N RGD:5509061 20220811 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11994405 1316076 Sbf1 SET binding factor 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20220811 MGI PMID:34718573 1316076 Sbf1 SET binding factor 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20220811 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20220811 MGI PMID:34718573 1316076 Sbf1 SET binding factor 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220811 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:11994405 1316076 Sbf1 SET binding factor 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:11994405 1316076 Sbf1 SET binding factor 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220811 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20210826 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11994405 1316076 Sbf1 SET binding factor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20220811 MGI PMID:34718573 1316076 Sbf1 SET binding factor 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20231207 MGI 1316076 Sbf1 SET binding factor 1 gene MP:0020452 abnormal axon radial sorting IAGP N RGD:5509061 20220811 MGI PMID:34718573 1316076 Sbf1 SET binding factor 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220811 MGI 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0009488 abnormal pancreatic islet cell apoptosis IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316078 Tfb2m transcription factor B2, mitochondrial gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20210805 MGI PMID:28702322 1316081 Ppef2 protein phosphatase, EF hand calcium-binding domain 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11713293 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:24141881 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:24141881 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:24141881 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:24141881 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:24141881 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:24141881 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24141881 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0008276 failure of intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:24141881 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20141003 MGI PMID:24141881 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0010587 conotruncal ridge hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0010589 common truncal valve IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0010652 absent aorticopulmonary septum IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19412548 1316082 Pds5a PDS5 cohesin associated factor A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24141881 1316084 Rab5c RAB5C, member RAS oncogene family gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1316084 Rab5c RAB5C, member RAS oncogene family gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1316084 Rab5c RAB5C, member RAS oncogene family gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 1316084 Rab5c RAB5C, member RAS oncogene family gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1316084 Rab5c RAB5C, member RAS oncogene family gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0000111 cleft palate IEA N RGD:5509061 20230601 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20210128 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0000599 enlarged liver IEA N RGD:5509061 20210520 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20210128 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0001785 edema IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0003717 pallor IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20220519 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0004848 abnormal liver size IEA N RGD:5509061 20210128 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0008443 absent subplate IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20231130 MGI PMID:30428088 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0011724 ectopic cortical neuron IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0012139 increased forebrain size IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0014558 decreased cortical ventricular zone thickness IAGP N RGD:5509061 20241031 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0020067 increased neocortex size IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316087 Wdfy3 WD repeat and FYVE domain containing 3 gene MP:0020389 increased radial glial cell number IAGP N RGD:5509061 20170314 MGI PMID:25198012 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20200521 MGI PMID:32142668 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16436615 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19596243 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:16436615 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20210805 MGI PMID:30514900 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:23197710 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20200521 MGI PMID:32142668 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:16436615 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:19596243 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:11955447 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:11955448 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:12121626 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:22036570 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:22318233 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20190912 MGI PMID:31305241 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16436615 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20151203 MGI PMID:24423059 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:11955447 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:11955448 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:12121626 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:23197710 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20210805 MGI PMID:30514900 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:12121626 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:19596243 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:22036570 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:22318233 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22318233 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:22318233 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:24210822 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22295099 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210805 MGI PMID:30514900 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19596243 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19596243 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20200521 MGI PMID:32142668 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:11955448 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210805 MGI PMID:30514900 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:12121626 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:12121626 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16436615 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:11955448 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:12121626 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:19596243 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18691547 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20210805 MGI PMID:30514900 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20210805 MGI PMID:30514900 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20210805 MGI PMID:30514900 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:24210822 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0003647 absent oligodendrocytes IAGP N RGD:5509061 20141003 MGI PMID:11955447 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20200521 MGI PMID:32142668 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:11955447 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:12121626 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:11955447 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22318233 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24179156 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:12121626 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20200521 MGI PMID:32142668 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12121626 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:22036570 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:11955448 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18691547 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22036570 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20210805 MGI PMID:30514900 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:24210822 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20220324 MGI PMID:35022234 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20200521 MGI PMID:32142668 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22295099 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0009684 abnormal spinal cord lateral motor column morphology IAGP N RGD:5509061 20141003 MGI PMID:22036570 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0009684 abnormal spinal cord lateral motor column morphology IAGP N RGD:5509061 20190912 MGI PMID:31305241 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0009685 abnormal spinal cord motor column morphology IAGP N RGD:5509061 20141003 MGI PMID:22036570 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0009686 abnormal spinal cord medial motor column morphology IAGP N RGD:5509061 20141003 MGI PMID:22036570 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20210805 MGI PMID:30514900 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20220324 MGI PMID:35022234 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20210805 MGI PMID:30514900 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20200521 MGI PMID:32142668 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20200521 MGI PMID:32142668 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19596243 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20826664 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200521 MGI PMID:32142668 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12121626 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22036570 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11955447 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22036570 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22036570 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11955448 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22036570 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200521 MGI PMID:32142668 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20210805 MGI PMID:30514900 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20210805 MGI PMID:30514900 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20220324 MGI PMID:35022234 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0021103 abnormal ventral interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:22036570 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:11955447 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:11955448 1316089 Olig2 oligodendrocyte transcription factor 2 gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:22036570 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0000111 cleft palate IEA N RGD:5509061 20141003 MGI 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18219393 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:18219393 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18219393 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20160811 MGI 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0003330 abnormal auditory tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18219393 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:18219393 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18219393 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0006018 abnormal tympanic membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:18219393 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0009891 abnormal palate bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18219393 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18219393 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0011087 neonatal lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0020900 abnormal middle ear epithelium morphology IAGP N RGD:5509061 20191219 MGI PMID:18219393 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0020903 increased middle ear goblet cell number IAGP N RGD:5509061 20191219 MGI PMID:18219393 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0030154 abnormal tympanic cavity morphology IAGP N RGD:5509061 20171005 MGI PMID:18219393 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0030226 middle ear polyps IAGP N RGD:5509061 20171019 MGI PMID:18219393 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0030410 middle ear effusion IAGP N RGD:5509061 20171207 MGI PMID:18219393 1316091 Eya4 EYA transcriptional coactivator and phosphatase 4 gene MP:0030413 tympanic membrane retraction IAGP N RGD:5509061 20171207 MGI PMID:18219393 1316094 Lmo2 LIM domain only 2 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:8033210 1316094 Lmo2 LIM domain only 2 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:8033210 1316094 Lmo2 LIM domain only 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:12781363 1316094 Lmo2 LIM domain only 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12781363 1316094 Lmo2 LIM domain only 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16096649 1316094 Lmo2 LIM domain only 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8033210 1316094 Lmo2 LIM domain only 2 gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20141003 MGI PMID:8033210 1316094 Lmo2 LIM domain only 2 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:8033210 1316094 Lmo2 LIM domain only 2 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:8033210 1316094 Lmo2 LIM domain only 2 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:12781363 1316094 Lmo2 LIM domain only 2 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:16096649 1316094 Lmo2 LIM domain only 2 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10618416 1316094 Lmo2 LIM domain only 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12781363 1316094 Lmo2 LIM domain only 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:8033210 1316094 Lmo2 LIM domain only 2 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:16096649 1316094 Lmo2 LIM domain only 2 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:16096649 1316094 Lmo2 LIM domain only 2 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20150409 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8033210 1316094 Lmo2 LIM domain only 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:8033210 1316094 Lmo2 LIM domain only 2 gene MP:0003794 delayed somite formation IAGP N RGD:5509061 20141003 MGI PMID:8033210 1316094 Lmo2 LIM domain only 2 gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:8033210 1316094 Lmo2 LIM domain only 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:8033210 1316094 Lmo2 LIM domain only 2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:12781363 1316094 Lmo2 LIM domain only 2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16096649 1316094 Lmo2 LIM domain only 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8033210 1316094 Lmo2 LIM domain only 2 gene MP:0012131 small visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:8033210 1316094 Lmo2 LIM domain only 2 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:8033210 1316094 Lmo2 LIM domain only 2 gene MP:0013657 abnormal blood cell morphology IAGP N RGD:5509061 20150409 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20150409 MGI PMID:19966810 1316094 Lmo2 LIM domain only 2 gene MP:0013705 decreased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20150409 MGI PMID:19966810 1316098 Prpf6 pre-mRNA splicing factor 6 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 1316098 Prpf6 pre-mRNA splicing factor 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1316098 Prpf6 pre-mRNA splicing factor 6 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1316098 Prpf6 pre-mRNA splicing factor 6 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20170105 MGI 1316098 Prpf6 pre-mRNA splicing factor 6 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170105 MGI 1316098 Prpf6 pre-mRNA splicing factor 6 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1316098 Prpf6 pre-mRNA splicing factor 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316098 Prpf6 pre-mRNA splicing factor 6 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1316103 Ankrd27 ankyrin repeat domain 27 gene MP:0002764 short tibia IEA N RGD:5509061 20160421 MGI 1316103 Ankrd27 ankyrin repeat domain 27 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20160421 MGI 1316104 Pigz phosphatidylinositol glycan anchor biosynthesis, class Z gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1316104 Pigz phosphatidylinositol glycan anchor biosynthesis, class Z gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210826 MGI 1316104 Pigz phosphatidylinositol glycan anchor biosynthesis, class Z gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210826 MGI 1316108 Ndufs2 NADH:ubiquinone oxidoreductase core subunit S2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1316108 Ndufs2 NADH:ubiquinone oxidoreductase core subunit S2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1316108 Ndufs2 NADH:ubiquinone oxidoreductase core subunit S2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1316108 Ndufs2 NADH:ubiquinone oxidoreductase core subunit S2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1316114 Fignl1 fidgetin-like 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20231123 MGI PMID:37891173 1316114 Fignl1 fidgetin-like 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20231123 MGI PMID:37891173 1316114 Fignl1 fidgetin-like 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20231123 MGI PMID:37891173 1316114 Fignl1 fidgetin-like 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20231123 MGI PMID:37891173 1316114 Fignl1 fidgetin-like 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20231123 MGI PMID:37891173 1316114 Fignl1 fidgetin-like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316116 Zfand3 zinc finger, AN1-type domain 3 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1316116 Zfand3 zinc finger, AN1-type domain 3 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1316116 Zfand3 zinc finger, AN1-type domain 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1316116 Zfand3 zinc finger, AN1-type domain 3 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20231207 MGI 1316116 Zfand3 zinc finger, AN1-type domain 3 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1316116 Zfand3 zinc finger, AN1-type domain 3 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20230601 MGI 1316116 Zfand3 zinc finger, AN1-type domain 3 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1316116 Zfand3 zinc finger, AN1-type domain 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1316116 Zfand3 zinc finger, AN1-type domain 3 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1316118 Ndufb9 NADH:ubiquinone oxidoreductase subunit B9 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1316118 Ndufb9 NADH:ubiquinone oxidoreductase subunit B9 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1316118 Ndufb9 NADH:ubiquinone oxidoreductase subunit B9 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1316118 Ndufb9 NADH:ubiquinone oxidoreductase subunit B9 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1316118 Ndufb9 NADH:ubiquinone oxidoreductase subunit B9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316120 Cenpe centromere protein E gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1316120 Cenpe centromere protein E gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 1316120 Cenpe centromere protein E gene MP:0002658 abnormal liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:12361599 1316120 Cenpe centromere protein E gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:12361599 1316120 Cenpe centromere protein E gene MP:0004966 abnormal inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:12361599 1316120 Cenpe centromere protein E gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:12361599 1316120 Cenpe centromere protein E gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12361599 1316120 Cenpe centromere protein E gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316120 Cenpe centromere protein E gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 1316120 Cenpe centromere protein E gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 1316123 Cxcl11 chemokine (C-X-C motif) ligand 11 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20240418 MGI PMID:35233830 1316123 Cxcl11 chemokine (C-X-C motif) ligand 11 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20240418 MGI PMID:35233830 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20190530 MGI PMID:30622831 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20190530 MGI PMID:30622831 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20181018 MGI PMID:29428562 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0000692 small spleen IEA N RGD:5509061 20210826 MGI 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0001127 small ovary IEA N RGD:5509061 20210826 MGI 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190530 MGI PMID:30622831 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0001293 anophthalmia IEA N RGD:5509061 20231207 MGI 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0001577 anemia IAGP N RGD:5509061 20190530 MGI PMID:30622831 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20181018 MGI PMID:29428562 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20181227 MGI 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20181018 MGI PMID:29428562 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20181018 MGI PMID:29428562 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0002284 abnormal tracheal smooth muscle morphology IAGP N RGD:5509061 20181018 MGI PMID:29428562 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20190530 MGI PMID:30622831 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0002637 small uterus IEA N RGD:5509061 20210826 MGI 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20190530 MGI PMID:30622831 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20190530 MGI PMID:30622831 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20181018 MGI PMID:29428562 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0003604 single kidney IAGP N RGD:5509061 20190530 MGI PMID:26926082 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0003668 abnormal periodontal ligament morphology IAGP N RGD:5509061 20190530 MGI PMID:26926082 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20190530 MGI PMID:26926082 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0003933 abnormal cementum morphology IAGP N RGD:5509061 20190530 MGI PMID:26926082 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20190530 MGI PMID:26926082 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20190530 MGI PMID:30622831 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20190530 MGI PMID:30622831 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0004149 increased bone strength IAGP N RGD:5509061 20190530 MGI PMID:30622831 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0004551 decreased tracheal cartilage ring number IAGP N RGD:5509061 20181018 MGI PMID:29428562 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20240523 MGI 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210826 MGI 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0010883 trachea stenosis IAGP N RGD:5509061 20181018 MGI PMID:29428562 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20190530 MGI PMID:26926082 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0013251 dental pulp necrosis IAGP N RGD:5509061 20190530 MGI PMID:26926082 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0013496 abnormal trachea development IAGP N RGD:5509061 20181018 MGI PMID:29428562 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0013623 increased femur compact bone thickness IAGP N RGD:5509061 20190530 MGI PMID:30622831 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20190530 MGI PMID:30622831 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0030101 carious teeth IAGP N RGD:5509061 20190530 MGI PMID:26926082 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0030132 periodontium inflammation IAGP N RGD:5509061 20190530 MGI PMID:26926082 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0030453 abnormal odontoblast morphology IAGP N RGD:5509061 20190530 MGI PMID:26926082 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0030463 apical tooth abscess IAGP N RGD:5509061 20190530 MGI PMID:26926082 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0030494 abnormal molar root morphology IAGP N RGD:5509061 20190530 MGI PMID:26926082 1316125 Notum notum palmitoleoyl-protein carboxylesterase gene MP:0030542 abnormal dentin development IAGP N RGD:5509061 20190530 MGI PMID:26926082 1316127 Snrnp70 small nuclear ribonucleoprotein 70 (U1) gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241010 MGI 1316127 Snrnp70 small nuclear ribonucleoprotein 70 (U1) gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241017 MGI 1316127 Snrnp70 small nuclear ribonucleoprotein 70 (U1) gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241017 MGI 1316127 Snrnp70 small nuclear ribonucleoprotein 70 (U1) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20221215 MGI 1316130 Zc2hc1c zinc finger, C2HC-type containing 1C gene MP:0000160 kyphosis IEA N RGD:5509061 20220811 MGI 1316130 Zc2hc1c zinc finger, C2HC-type containing 1C gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220811 MGI 1316130 Zc2hc1c zinc finger, C2HC-type containing 1C gene MP:0000274 enlarged heart IEA N RGD:5509061 20220811 MGI 1316130 Zc2hc1c zinc finger, C2HC-type containing 1C gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220811 MGI 1316130 Zc2hc1c zinc finger, C2HC-type containing 1C gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220811 MGI 1316130 Zc2hc1c zinc finger, C2HC-type containing 1C gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220811 MGI 1316130 Zc2hc1c zinc finger, C2HC-type containing 1C gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220811 MGI 1316130 Zc2hc1c zinc finger, C2HC-type containing 1C gene MP:0001147 small testis IEA N RGD:5509061 20220811 MGI 1316130 Zc2hc1c zinc finger, C2HC-type containing 1C gene MP:0001148 enlarged testis IEA N RGD:5509061 20220811 MGI 1316130 Zc2hc1c zinc finger, C2HC-type containing 1C gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220811 MGI 1316130 Zc2hc1c zinc finger, C2HC-type containing 1C gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20221215 MGI 1316130 Zc2hc1c zinc finger, C2HC-type containing 1C gene MP:0009709 hydrometra IEA N RGD:5509061 20220811 MGI 1316131 Pcdhb9 protocadherin beta 9 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1316131 Pcdhb9 protocadherin beta 9 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1316131 Pcdhb9 protocadherin beta 9 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1316131 Pcdhb9 protocadherin beta 9 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20230601 MGI 1316132 Ankrd52 ankyrin repeat domain 52 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1316132 Ankrd52 ankyrin repeat domain 52 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1316132 Ankrd52 ankyrin repeat domain 52 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1316132 Ankrd52 ankyrin repeat domain 52 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1316132 Ankrd52 ankyrin repeat domain 52 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210128 MGI 1316132 Ankrd52 ankyrin repeat domain 52 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1316132 Ankrd52 ankyrin repeat domain 52 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200402 MGI 1316132 Ankrd52 ankyrin repeat domain 52 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316134 Kctd11 potassium channel tetramerisation domain containing 11 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1316134 Kctd11 potassium channel tetramerisation domain containing 11 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20220811 MGI 1316147 Lamtor3 late endosomal/lysosomal adaptor, MAPK and MTOR activator 3 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20230119 MGI 1316147 Lamtor3 late endosomal/lysosomal adaptor, MAPK and MTOR activator 3 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20230119 MGI 1316147 Lamtor3 late endosomal/lysosomal adaptor, MAPK and MTOR activator 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1316150 Zfp42 zinc finger protein 42 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1316150 Zfp42 zinc finger protein 42 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21233130 1316150 Zfp42 zinc finger protein 42 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21641340 1316150 Zfp42 zinc finger protein 42 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1316150 Zfp42 zinc finger protein 42 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:21641340 1316150 Zfp42 zinc finger protein 42 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:21233130 1316150 Zfp42 zinc finger protein 42 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:21641340 1316150 Zfp42 zinc finger protein 42 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20201022 MGI 1316150 Zfp42 zinc finger protein 42 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18433507 1316150 Zfp42 zinc finger protein 42 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21233130 1316150 Zfp42 zinc finger protein 42 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:21641340 1316150 Zfp42 zinc finger protein 42 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:21641340 1316150 Zfp42 zinc finger protein 42 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21233130 1316150 Zfp42 zinc finger protein 42 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21233130 1316150 Zfp42 zinc finger protein 42 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1316152 Zfp367 zinc finger protein 367 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20160804 MGI 1316153 Shc2 SHC (Src homology 2 domain containing) transforming protein 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11163269 1316153 Shc2 SHC (Src homology 2 domain containing) transforming protein 2 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:11163269 1316153 Shc2 SHC (Src homology 2 domain containing) transforming protein 2 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11163269 1316153 Shc2 SHC (Src homology 2 domain containing) transforming protein 2 gene MP:0000969 abnormal nociceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:11163269 1316153 Shc2 SHC (Src homology 2 domain containing) transforming protein 2 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:11163269 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20201022 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:22490684 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20190502 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18523150 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:18451267 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:18523150 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0000414 alopecia IAGP N RGD:5509061 20170406 MGI PMID:23300183 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0000418 focal hair loss IEA N RGD:5509061 20161201 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18451267 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20190502 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20190502 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18523150 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0001586 abnormal erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22490684 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0001670 abnormal intestinal mineral absorption IAGP N RGD:5509061 20141003 MGI PMID:18451267 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18523150 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:18523150 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0001923 reduced female fertility IEA N RGD:5509061 20111116 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18451267 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18523150 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20190502 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002224 abnormal spleen size IAGP N RGD:5509061 20141003 MGI PMID:22490684 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18523150 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22490684 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:18451267 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:22490684 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20170406 MGI PMID:23300183 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20170406 MGI PMID:23300183 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:18523150 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:18451267 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:22490684 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:18451267 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:22490684 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0003582 abnormal ovary development IAGP N RGD:5509061 20141003 MGI PMID:18523150 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:18523150 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:18451267 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:18523150 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20170406 MGI PMID:23300183 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0005387 immune system phenotype IEA N RGD:5509061 20201022 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20170406 MGI PMID:23300183 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0005563 abnormal hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:22490684 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18451267 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20170406 MGI PMID:23300183 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20201022 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201022 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0008738 abnormal liver iron level IAGP N RGD:5509061 20141003 MGI PMID:22490684 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0008739 abnormal spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:22490684 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20170406 MGI PMID:23300183 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22490684 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:18451267 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20141003 MGI PMID:22490684 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20141003 MGI PMID:18451267 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20190502 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0010682 abnormal hair follicle infundibulum morphology IAGP N RGD:5509061 20141003 MGI PMID:18523150 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0010689 thin hair follicle outer root sheath IAGP N RGD:5509061 20141003 MGI PMID:18523150 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201022 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0011284 abnormal circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:22490684 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:22490684 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0011896 increased circulating unsaturated transferrin level IAGP N RGD:5509061 20170406 MGI PMID:23300183 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20190502 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0013303 decreased pancreas iron level IAGP N RGD:5509061 20161020 MGI PMID:20200349 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0013648 increased CD11b-high dendritic cell number IEA N RGD:5509061 20211021 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0013676 increased Ly6C-positive mature NK cell number IEA N RGD:5509061 20201022 MGI 1316155 Tmprss6 transmembrane serine protease 6 gene MP:0020368 decreased heart iron level IAGP N RGD:5509061 20161020 MGI PMID:20200349 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20170105 MGI 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:19841728 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19114557 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170105 MGI 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1316157 Ercc3 excision repair cross-complementing rodent repair deficiency, complementation group 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1316160 Pls1 plastin 1 (I-isoform) gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20150129 MGI PMID:19321664 1316160 Pls1 plastin 1 (I-isoform) gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20150129 MGI PMID:25124451 1316160 Pls1 plastin 1 (I-isoform) gene MP:0004525 thin cochlear hair cell stereocilia IAGP N RGD:5509061 20150129 MGI PMID:25124451 1316160 Pls1 plastin 1 (I-isoform) gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20150129 MGI PMID:25124451 1316160 Pls1 plastin 1 (I-isoform) gene MP:0004528 fused outer hair cell stereocilia IAGP N RGD:5509061 20150129 MGI PMID:25124451 1316160 Pls1 plastin 1 (I-isoform) gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20150129 MGI PMID:25124451 1316160 Pls1 plastin 1 (I-isoform) gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20150129 MGI PMID:25124451 1316160 Pls1 plastin 1 (I-isoform) gene MP:0004536 short inner hair cell stereocilia IAGP N RGD:5509061 20150129 MGI PMID:25124451 1316160 Pls1 plastin 1 (I-isoform) gene MP:0006325 impaired hearing IAGP N RGD:5509061 20150129 MGI PMID:25124451 1316160 Pls1 plastin 1 (I-isoform) gene MP:0008141 decreased small intestinal microvillus size IAGP N RGD:5509061 20150129 MGI PMID:19321664 1316160 Pls1 plastin 1 (I-isoform) gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20150129 MGI PMID:19321664 1316160 Pls1 plastin 1 (I-isoform) gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20150129 MGI PMID:19321664 1316160 Pls1 plastin 1 (I-isoform) gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20150129 MGI PMID:19321664 1316160 Pls1 plastin 1 (I-isoform) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20150129 MGI PMID:25124451 1316160 Pls1 plastin 1 (I-isoform) gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20150129 MGI PMID:19321664 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:19622764 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:19622764 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:19622764 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19622764 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:19622764 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19617532 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:19622764 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:19622764 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0003668 abnormal periodontal ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:19622764 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:19617532 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19617532 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0010747 abnormal enamel organ morphology IAGP N RGD:5509061 20180125 MGI PMID:19622764 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0013258 abnormal extracellular matrix morphology IAGP N RGD:5509061 20141003 MGI PMID:19622764 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0030083 long upper incisors IAGP N RGD:5509061 20180125 MGI PMID:19622764 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20180125 MGI PMID:19617532 1316163 Antxr1 anthrax toxin receptor 1 gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20180125 MGI PMID:19622764 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316167 Dusp22 dual specificity phosphatase 22 gene MP:0011567 increased renal glomerulus lobularity IAGP N RGD:5509061 20191226 MGI PMID:24714587 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141211 MGI PMID:16598045 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0000791 delaminated cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11929848 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15905400 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:11929848 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:11929848 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20141003 MGI PMID:11929848 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20111116 MGI 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11929848 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20200910 MGI PMID:16598045 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001577 anemia IEA N RGD:5509061 20111116 MGI 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141211 MGI PMID:16598045 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20200910 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141211 MGI PMID:16598045 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20200910 MGI PMID:15905400 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15905400 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001924 infertility IEA N RGD:5509061 20111116 MGI 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141211 MGI PMID:16598045 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141211 MGI PMID:16598045 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141211 MGI PMID:16598045 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:15905400 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:15905400 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0002959 increased urine microalbumin level IAGP N RGD:5509061 20141211 MGI PMID:16598045 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0003236 abnormal lens capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0003381 vitreal fibroplasia IAGP N RGD:5509061 20141003 MGI PMID:11929848 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0003954 abnormal Reichert's membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:15905400 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141211 MGI PMID:16598045 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0005161 hematuria IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0006203 eye hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0009026 abnormal brain pia mater morphology IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0009274 buphthalmos IAGP N RGD:5509061 20141003 MGI PMID:11929848 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0009275 bruising IAGP N RGD:5509061 20141003 MGI PMID:11929848 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20141211 MGI PMID:16598045 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0010235 abnormal retina inner limiting membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0010252 anterior subcapsular cataract IAGP N RGD:5509061 20141003 MGI PMID:11929848 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0010259 anterior polar cataract IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0010261 sutural cataract IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0010263 total cataract IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15905400 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15905400 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011187 abnormal parietal endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15905400 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:21625620 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011402 renal cast IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011419 erythrocyturia IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141003 MGI PMID:11929848 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011498 abnormal glomerular capsule parietal layer morphology IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011502 parietal capsular epithelium metaplasia IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011509 dilated glomerular capillary IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:17179069 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0011843 abnormal kidney collecting duct epithelium morphology IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0020153 abnormal urine albumin level IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20170803 MGI PMID:26260163 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0021002 brain lesion IAGP N RGD:5509061 20210805 MGI PMID:15905400 1316171 Col4a1 collagen, type IV, alpha 1 gene MP:0031109 subarachnoid hemorrhage IAGP N RGD:5509061 20200910 MGI PMID:16598045 1316173 Spink8 serine peptidase inhibitor, Kazal type 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1316179 Mettl26 methyltransferase like 26 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1316179 Mettl26 methyltransferase like 26 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1316181 Pigt phosphatidylinositol glycan anchor biosynthesis, class T gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170413 MGI 1316184 Ccdc186 coiled-coil domain containing 186 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20230601 MGI 1316184 Ccdc186 coiled-coil domain containing 186 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1316184 Ccdc186 coiled-coil domain containing 186 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230601 MGI 1316184 Ccdc186 coiled-coil domain containing 186 gene MP:0001785 edema IEA N RGD:5509061 20230601 MGI 1316184 Ccdc186 coiled-coil domain containing 186 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1316184 Ccdc186 coiled-coil domain containing 186 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1316184 Ccdc186 coiled-coil domain containing 186 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1316184 Ccdc186 coiled-coil domain containing 186 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316193 Tyk2 tyrosine kinase 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1316193 Tyk2 tyrosine kinase 2 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220519 MGI 1316193 Tyk2 tyrosine kinase 2 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20220519 MGI 1316193 Tyk2 tyrosine kinase 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23217260 1316193 Tyk2 tyrosine kinase 2 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:23217260 1316193 Tyk2 tyrosine kinase 2 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23217260 1316193 Tyk2 tyrosine kinase 2 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23217260 1316193 Tyk2 tyrosine kinase 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11313413 1316193 Tyk2 tyrosine kinase 2 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20220519 MGI 1316193 Tyk2 tyrosine kinase 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1316193 Tyk2 tyrosine kinase 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23217260 1316193 Tyk2 tyrosine kinase 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11070174 1316193 Tyk2 tyrosine kinase 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11070174 1316193 Tyk2 tyrosine kinase 2 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:23217260 1316193 Tyk2 tyrosine kinase 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:14617019 1316193 Tyk2 tyrosine kinase 2 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:11313413 1316193 Tyk2 tyrosine kinase 2 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16148148 1316193 Tyk2 tyrosine kinase 2 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23217260 1316193 Tyk2 tyrosine kinase 2 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:23217260 1316193 Tyk2 tyrosine kinase 2 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:16148148 1316193 Tyk2 tyrosine kinase 2 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:11313414 1316193 Tyk2 tyrosine kinase 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23217260 1316193 Tyk2 tyrosine kinase 2 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:11313413 1316193 Tyk2 tyrosine kinase 2 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:23217260 1316193 Tyk2 tyrosine kinase 2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14617019 1316193 Tyk2 tyrosine kinase 2 gene MP:0008124 decreased plasmacytoid dendritic cell number IEA N RGD:5509061 20220519 MGI 1316193 Tyk2 tyrosine kinase 2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11313413 1316193 Tyk2 tyrosine kinase 2 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:11313413 1316193 Tyk2 tyrosine kinase 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11070173 1316193 Tyk2 tyrosine kinase 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11070174 1316193 Tyk2 tyrosine kinase 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11313413 1316193 Tyk2 tyrosine kinase 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11313414 1316193 Tyk2 tyrosine kinase 2 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:11313414 1316193 Tyk2 tyrosine kinase 2 gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11070174 1316193 Tyk2 tyrosine kinase 2 gene MP:0009791 increased susceptibility to viral infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11070173 1316193 Tyk2 tyrosine kinase 2 gene MP:0010580 decreased heart left ventricle size IEA N RGD:5509061 20240523 MGI 1316193 Tyk2 tyrosine kinase 2 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:23217260 1316193 Tyk2 tyrosine kinase 2 gene MP:0011077 decreased macrophage nitric oxide production IAGP N RGD:5509061 20141003 MGI PMID:11070173 1316193 Tyk2 tyrosine kinase 2 gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23217260 1316193 Tyk2 tyrosine kinase 2 gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20141003 MGI PMID:23217260 1316193 Tyk2 tyrosine kinase 2 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:11070173 1316193 Tyk2 tyrosine kinase 2 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:16148148 1316193 Tyk2 tyrosine kinase 2 gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:22723949 1316193 Tyk2 tyrosine kinase 2 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:16148148 1316193 Tyk2 tyrosine kinase 2 gene MP:0031040 increased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:22723949 1316199 Leprotl1 leptin receptor overlapping transcript-like 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1316199 Leprotl1 leptin receptor overlapping transcript-like 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1316199 Leprotl1 leptin receptor overlapping transcript-like 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20201231 MGI 1316199 Leprotl1 leptin receptor overlapping transcript-like 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1316199 Leprotl1 leptin receptor overlapping transcript-like 1 gene MP:0002626 increased heart rate IEA N RGD:5509061 20210128 MGI 1316199 Leprotl1 leptin receptor overlapping transcript-like 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1316199 Leprotl1 leptin receptor overlapping transcript-like 1 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20210128 MGI 1316199 Leprotl1 leptin receptor overlapping transcript-like 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1316199 Leprotl1 leptin receptor overlapping transcript-like 1 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20201231 MGI 1316199 Leprotl1 leptin receptor overlapping transcript-like 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201231 MGI 1316199 Leprotl1 leptin receptor overlapping transcript-like 1 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20230601 MGI 1316199 Leprotl1 leptin receptor overlapping transcript-like 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1316204 Ahsa2 AHA1, activator of heat shock protein ATPase 2 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210826 MGI 1316204 Ahsa2 AHA1, activator of heat shock protein ATPase 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1316205 Got1l1 glutamic-oxaloacetic transaminase 1-like 1 gene MP:0030707 decreased glutamine level IAGP N RGD:5509061 20210415 MGI PMID:25287256 1316205 Got1l1 glutamic-oxaloacetic transaminase 1-like 1 gene MP:0030737 decreased glutamic acid level IAGP N RGD:5509061 20210415 MGI PMID:25287256 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17267394 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17540762 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:17267394 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:17577581 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:17540762 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17142808 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17267394 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17577581 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17142808 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17267394 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17577581 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17577581 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17142808 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:17540762 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17267394 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17577581 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:17142808 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:17540762 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0004781 abnormal surfactant composition IAGP N RGD:5509061 20141003 MGI PMID:17267394 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20141003 MGI PMID:17540762 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20141003 MGI PMID:17577581 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:17142808 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:17577581 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:17267394 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:17267394 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:17577581 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0010814 absent alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:17142808 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0010814 absent alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:17267394 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0010814 absent alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:17540762 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0010817 absent type I pneumocytes IAGP N RGD:5509061 20141003 MGI PMID:17267394 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:17142808 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:17267394 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0010890 decreased alveolar lamellar body number IAGP N RGD:5509061 20141003 MGI PMID:17540762 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0010897 abnormal bronchiole epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17267394 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0010909 pulmonary alveolar hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17142808 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17142808 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17267394 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17540762 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17577581 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17540762 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:17267394 1316208 Abca3 ATP-binding cassette, sub-family A member 3 gene MP:0011163 increased wet-to-dry lung weight ratio IAGP N RGD:5509061 20141003 MGI PMID:17267394 1316211 Dpt dermatopontin gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:12230512 1316211 Dpt dermatopontin gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:12230512 1316211 Dpt dermatopontin gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:16877395 1316211 Dpt dermatopontin gene MP:0003094 abnormal cornea posterior stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:16877395 1316211 Dpt dermatopontin gene MP:0005275 abnormal skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:12230512 1316211 Dpt dermatopontin gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:16877395 1316211 Dpt dermatopontin gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:12230512 1316211 Dpt dermatopontin gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:16877395 1316211 Dpt dermatopontin gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:12230512 1316211 Dpt dermatopontin gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12230512 1316213 Jakmip3 janus kinase and microtubule interacting protein 3 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20240523 MGI 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:19581591 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15347806 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:15347806 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:15347806 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15347806 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:15347806 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:15347806 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15347806 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19581591 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:19581591 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:19581591 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:15347806 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19581591 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0004167 abnormal cingulate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:19581591 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0008534 enlarged fourth ventricle IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:19581591 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0010901 abnormal pulmonary alveolar parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:19581591 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0010935 increased airway resistance IAGP N RGD:5509061 20141003 MGI PMID:19581591 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0011012 bronchiectasis IAGP N RGD:5509061 20141003 MGI PMID:19581591 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0011026 impaired branching involved in trachea morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19581591 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19581591 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0012489 abnormal retrosplenial region morphology IAGP N RGD:5509061 20141003 MGI PMID:16190882 1316219 Npas3 neuronal PAS domain protein 3 gene MP:0031442 enlarged cerebral aqueduct IAGP N RGD:5509061 20221103 MGI PMID:16190882 1316220 Trem6l triggering receptor expressed on myeloid cells-like 6 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20240523 MGI 1316220 Trem6l triggering receptor expressed on myeloid cells-like 6 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20240523 MGI 1316220 Trem6l triggering receptor expressed on myeloid cells-like 6 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20240523 MGI 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210506 MGI PMID:26136667 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20210506 MGI PMID:26136667 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20210520 MGI 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20210506 MGI PMID:26136667 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20210506 MGI PMID:26136667 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20210506 MGI PMID:26136667 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20210506 MGI PMID:26136667 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20210506 MGI PMID:26136667 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0003908 decreased stereotypic behavior IAGP N RGD:5509061 20210506 MGI PMID:26136667 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20210415 MGI PMID:30673609 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210520 MGI 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20210506 MGI PMID:26136667 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20210506 MGI PMID:26136667 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20210506 MGI PMID:26136667 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20210506 MGI PMID:26136667 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200514 MGI 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20210415 MGI PMID:30673609 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 1316226 Cbarp calcium channel, voltage-dependent, beta subunit associated regulatory protein gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20210506 MGI PMID:26136667 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:9359707 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:9359707 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:9359707 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12391023 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:12055593 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9359707 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23023393 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002219 decreased lymph node number IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002343 abnormal lymph node cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002364 abnormal thymus size IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12055593 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:12055593 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002392 abnormal Peyer's patch T cell area morphology IAGP N RGD:5509061 20141003 MGI PMID:12055593 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:16973390 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:9359707 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9359707 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9359707 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:9359707 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12391023 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:9359707 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12055593 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12391023 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005046 absent spleen white pulp IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:9359707 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0005493 stomach epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0006173 abnormal myeloid dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12055593 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20190613 MGI 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008076 abnormal CD4-positive T cell differentiation IEA N RGD:5509061 20190613 MGI 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20190613 MGI 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008122 decreased myeloid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:12055593 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:12055593 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12055593 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008167 increased B-1a cell number IEA N RGD:5509061 20150702 MGI 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:12391023 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12391023 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16973390 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12391023 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12391023 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:16973390 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:16973390 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008240 abnormal spleen marginal zone macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008241 abnormal metallophilic macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:12391023 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008241 abnormal metallophilic macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008241 abnormal metallophilic macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008343 abnormal gamma-delta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21419662 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21419662 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:9359707 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:9407039 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008463 abnormal peripheral lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:12391023 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008463 abnormal peripheral lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008465 absent mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008471 abnormal spleen primary B follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008472 abnormal spleen secondary B follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12391023 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008473 abnormal spleen follicular dendritic cell network IAGP N RGD:5509061 20141003 MGI PMID:12391023 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008473 abnormal spleen follicular dendritic cell network IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008523 absent lymph node germinal center IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008524 increased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:12055593 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:9359707 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0009322 increased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9432976 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0009628 absent brachial lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0009633 absent cervical lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18025196 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9432973 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12391023 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0010798 abnormal stomach cardiac region morphology IAGP N RGD:5509061 20141003 MGI PMID:9314550 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0010851 decreased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190613 MGI 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17015635 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20170223 MGI PMID:20231695 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0013436 increased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20190613 MGI 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0020416 decreased fibroblast chemotaxis IAGP N RGD:5509061 20170223 MGI PMID:20231695 1316231 Nfkb2 nuclear factor of kappa light polypeptide gene enhancer in B cells 2, p49/p100 gene MP:0030505 tooth impaction IAGP N RGD:5509061 20191219 MGI PMID:9359707 1316233 Pum1 pumilio RNA-binding family member 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1316233 Pum1 pumilio RNA-binding family member 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1316233 Pum1 pumilio RNA-binding family member 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:22342750 1316233 Pum1 pumilio RNA-binding family member 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22342750 1316233 Pum1 pumilio RNA-binding family member 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 1316233 Pum1 pumilio RNA-binding family member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22342750 1316233 Pum1 pumilio RNA-binding family member 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:22342750 1316233 Pum1 pumilio RNA-binding family member 1 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22342750 1316233 Pum1 pumilio RNA-binding family member 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1316233 Pum1 pumilio RNA-binding family member 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22342750 1316233 Pum1 pumilio RNA-binding family member 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22342750 1316233 Pum1 pumilio RNA-binding family member 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1316233 Pum1 pumilio RNA-binding family member 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20160225 MGI PMID:25896760 1316233 Pum1 pumilio RNA-binding family member 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:22342750 1316237 Usp16 ubiquitin specific peptidase 16 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1316237 Usp16 ubiquitin specific peptidase 16 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1316237 Usp16 ubiquitin specific peptidase 16 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 1316237 Usp16 ubiquitin specific peptidase 16 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20111116 MGI 1316239 Myo10 myosin X gene MP:0000373 belly spot IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0000564 syndactyly IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0000585 kinked tail IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0000914 exencephaly IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0001265 decreased body size IEA N RGD:5509061 20141120 MGI 1316239 Myo10 myosin X gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0001293 anophthalmia IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0001297 microphthalmia IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1316239 Myo10 myosin X gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 1316239 Myo10 myosin X gene MP:0001307 fused cornea and lens IEA N RGD:5509061 20141003 MGI 1316239 Myo10 myosin X gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20150108 MGI 1316239 Myo10 myosin X gene MP:0001314 cornea opacity IEA N RGD:5509061 20141003 MGI 1316239 Myo10 myosin X gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20201231 MGI 1316239 Myo10 myosin X gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0001413 abnormal response to new environment IEA N RGD:5509061 20191128 MGI 1316239 Myo10 myosin X gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0001914 hemorrhage IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20170105 MGI 1316239 Myo10 myosin X gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20141120 MGI 1316239 Myo10 myosin X gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20170105 MGI 1316239 Myo10 myosin X gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20201231 MGI 1316239 Myo10 myosin X gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0002938 white spotting IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0003104 acrania IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0005174 abnormal tail pigmentation IEA N RGD:5509061 20141120 MGI 1316239 Myo10 myosin X gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1316239 Myo10 myosin X gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20150108 MGI 1316239 Myo10 myosin X gene MP:0008730 fused phalanges IEA N RGD:5509061 20141003 MGI 1316239 Myo10 myosin X gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0010714 iris coloboma IEA N RGD:5509061 20141120 MGI 1316239 Myo10 myosin X gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316239 Myo10 myosin X gene MP:0011277 decreased tail pigmentation IEA N RGD:5509061 20141120 MGI 1316239 Myo10 myosin X gene MP:0011877 absent liver IAGP N RGD:5509061 20180301 MGI PMID:29229982 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0000262 poor arterial differentiation IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:16061358 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:18505817 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:16061358 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16061358 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:16061358 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:16061358 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:16061358 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:16061358 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18505817 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20231109 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20231109 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16061358 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20231109 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:16061358 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:16061358 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20231109 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:22529374 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20240118 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20231109 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16061358 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0004937 dilated heart IAGP N RGD:5509061 20231109 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0005114 premature hair loss IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20231109 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16061358 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20231109 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231109 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:16061358 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20231109 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0008823 abnormal interventricular septum membranous part morphology IAGP N RGD:5509061 20231109 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0009163 absent pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:22529374 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22529374 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:16061358 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0009874 abnormal interdigital cell death IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20231109 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0010498 abnormal interventricular septum muscular part morphology IAGP N RGD:5509061 20231109 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20231109 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16061358 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18043734 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36325906 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0012254 absent intersomitic vessels IAGP N RGD:5509061 20141003 MGI PMID:16000382 1316243 Mib1 MIB E3 ubiquitin protein ligase 1 gene MP:0031525 thin left ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:36325906 1316247 Zfp612 zinc finger protein 612 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1316247 Zfp612 zinc finger protein 612 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1316247 Zfp612 zinc finger protein 612 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20160804 MGI 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21982646 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0001413 abnormal response to new environment IEA N RGD:5509061 20141003 MGI 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15466398 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21982646 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:15466398 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20160421 MGI 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0002321 hypoventilation IAGP N RGD:5509061 20141003 MGI PMID:15466398 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:21982646 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0002863 improved righting response IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0003578 absent ovary IEA N RGD:5509061 20160811 MGI 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20141003 MGI 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:21982646 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0005423 abnormal somatic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15466398 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21982646 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15466398 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18155191 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21982646 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0021210 bilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:21982646 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0021211 unilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:21982646 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0030190 small snout IAGP N RGD:5509061 20171019 MGI PMID:21982646 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0031447 unilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:21982646 1316249 Pbx3 pre B cell leukemia homeobox 3 gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:21982646 1316253 Ung uracil DNA glycosylase gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12934097 1316253 Ung uracil DNA glycosylase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12934097 1316253 Ung uracil DNA glycosylase gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12934097 1316253 Ung uracil DNA glycosylase gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12934097 1316253 Ung uracil DNA glycosylase gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:12934097 1316253 Ung uracil DNA glycosylase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22447450 1316253 Ung uracil DNA glycosylase gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12934097 1316253 Ung uracil DNA glycosylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12934097 1316253 Ung uracil DNA glycosylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22447450 1316253 Ung uracil DNA glycosylase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10912000 1316253 Ung uracil DNA glycosylase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12401169 1316253 Ung uracil DNA glycosylase gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:15199406 1316253 Ung uracil DNA glycosylase gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:19901081 1316253 Ung uracil DNA glycosylase gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:12401169 1316253 Ung uracil DNA glycosylase gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20210722 MGI PMID:31795137 1316253 Ung uracil DNA glycosylase gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:15199406 1316253 Ung uracil DNA glycosylase gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:12401169 1316253 Ung uracil DNA glycosylase gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:22447450 1316253 Ung uracil DNA glycosylase gene MP:0009796 abnormal base-excision repair IAGP N RGD:5509061 20141003 MGI PMID:22447450 1316253 Ung uracil DNA glycosylase gene MP:0009797 abnormal mismatch repair IAGP N RGD:5509061 20141003 MGI PMID:22447450 1316253 Ung uracil DNA glycosylase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22447450 1316253 Ung uracil DNA glycosylase gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22447450 1316256 Ubqlnl ubiquilin-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1316256 Ubqlnl ubiquilin-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26043068 1316259 Epha2 Eph receptor A2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:11287184 1316259 Epha2 Eph receptor A2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15054110 1316259 Epha2 Eph receptor A2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:11287184 1316259 Epha2 Eph receptor A2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:11287184 1316259 Epha2 Eph receptor A2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1316259 Epha2 Eph receptor A2 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16849550 1316259 Epha2 Eph receptor A2 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20180215 MGI PMID:28294115 1316259 Epha2 Eph receptor A2 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:19649315 1316259 Epha2 Eph receptor A2 gene MP:0001684 abnormal axial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11287184 1316259 Epha2 Eph receptor A2 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:11287184 1316259 Epha2 Eph receptor A2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11287184 1316259 Epha2 Eph receptor A2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8649815 1316259 Epha2 Eph receptor A2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1316259 Epha2 Eph receptor A2 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11287184 1316259 Epha2 Eph receptor A2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16849550 1316259 Epha2 Eph receptor A2 gene MP:0004713 split notochord IAGP N RGD:5509061 20141003 MGI PMID:11287184 1316259 Epha2 Eph receptor A2 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:11287184 1316259 Epha2 Eph receptor A2 gene MP:0010255 cortical cataract IAGP N RGD:5509061 20141003 MGI PMID:19649315 1316259 Epha2 Eph receptor A2 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20180215 MGI PMID:28294115 1316263 Ephx3 epoxide hydrolase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180125 MGI PMID:28384353 1316265 Lama1 laminin, alpha 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0001296 macrophthalmia IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20170105 MGI 1316265 Lama1 laminin, alpha 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1316265 Lama1 laminin, alpha 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 1316265 Lama1 laminin, alpha 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:15102706 1316265 Lama1 laminin, alpha 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15102706 1316265 Lama1 laminin, alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16100707 1316265 Lama1 laminin, alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:15668394 1316265 Lama1 laminin, alpha 1 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1316265 Lama1 laminin, alpha 1 gene MP:0003381 vitreal fibroplasia IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0003954 abnormal Reichert's membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:15668394 1316265 Lama1 laminin, alpha 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16100707 1316265 Lama1 laminin, alpha 1 gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:16100707 1316265 Lama1 laminin, alpha 1 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0009022 abnormal brain meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0009026 abnormal brain pia mater morphology IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0010235 abnormal retina inner limiting membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0010387 abnormal Bergmann glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15102706 1316265 Lama1 laminin, alpha 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15668394 1316265 Lama1 laminin, alpha 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16100707 1316265 Lama1 laminin, alpha 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316265 Lama1 laminin, alpha 1 gene MP:0011116 absent Reichert's membrane IAGP N RGD:5509061 20141003 MGI PMID:15102706 1316265 Lama1 laminin, alpha 1 gene MP:0011116 absent Reichert's membrane IAGP N RGD:5509061 20141003 MGI PMID:15668394 1316265 Lama1 laminin, alpha 1 gene MP:0011116 absent Reichert's membrane IAGP N RGD:5509061 20141003 MGI PMID:16100707 1316265 Lama1 laminin, alpha 1 gene MP:0011116 absent Reichert's membrane IAGP N RGD:5509061 20141003 MGI PMID:21983115 1316265 Lama1 laminin, alpha 1 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16100707 1316265 Lama1 laminin, alpha 1 gene MP:0011187 abnormal parietal endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16100707 1316265 Lama1 laminin, alpha 1 gene MP:0012671 retina spots IAGP N RGD:5509061 20141003 MGI PMID:20048158 1316265 Lama1 laminin, alpha 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16100707 1316266 Bahcc1 BAH domain and coiled-coil containing 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16807365 1316266 Bahcc1 BAH domain and coiled-coil containing 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16807365 1316266 Bahcc1 BAH domain and coiled-coil containing 1 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:16807365 1316266 Bahcc1 BAH domain and coiled-coil containing 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16807365 1316269 Mei1 meiotic double-stranded break formation protein 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:10700192 1316269 Mei1 meiotic double-stranded break formation protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10700192 1316269 Mei1 meiotic double-stranded break formation protein 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10700192 1316269 Mei1 meiotic double-stranded break formation protein 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:10700192 1316269 Mei1 meiotic double-stranded break formation protein 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:10700192 1316269 Mei1 meiotic double-stranded break formation protein 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23318132 1316269 Mei1 meiotic double-stranded break formation protein 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:10700192 1316272 Rnf44 ring finger protein 44 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1316272 Rnf44 ring finger protein 44 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1316272 Rnf44 ring finger protein 44 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1316272 Rnf44 ring finger protein 44 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1316280 Adgrg7 adhesion G protein-coupled receptor G7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180308 MGI PMID:24574718 1316280 Adgrg7 adhesion G protein-coupled receptor G7 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20211021 MGI 1316280 Adgrg7 adhesion G protein-coupled receptor G7 gene MP:0003291 interstinal hyperperistalsis IAGP N RGD:5509061 20180308 MGI PMID:24574718 1316280 Adgrg7 adhesion G protein-coupled receptor G7 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20211021 MGI 1316280 Adgrg7 adhesion G protein-coupled receptor G7 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180308 MGI PMID:24574718 1316280 Adgrg7 adhesion G protein-coupled receptor G7 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20211021 MGI 1316280 Adgrg7 adhesion G protein-coupled receptor G7 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0002764 short tibia IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0004658 abnormal ventral tubercle of atlas morphology IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0005364 increased susceptibility to prion infection IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0009787 increased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0011919 abnormal R wave IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0013670 increased Ly6C-positive immature NK cell number IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316282 Pgap4 post-GPI attachment to proteins GalNAc transferase 4 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20231026 MGI PMID:35151686 1316289 Dyrk1b dual-specificity tyrosine phosphorylation regulated kinase 1b gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1316289 Dyrk1b dual-specificity tyrosine phosphorylation regulated kinase 1b gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1316289 Dyrk1b dual-specificity tyrosine phosphorylation regulated kinase 1b gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1316289 Dyrk1b dual-specificity tyrosine phosphorylation regulated kinase 1b gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20201022 MGI 1316289 Dyrk1b dual-specificity tyrosine phosphorylation regulated kinase 1b gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20200402 MGI 1316289 Dyrk1b dual-specificity tyrosine phosphorylation regulated kinase 1b gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20240613 MGI PMID:35235343 1316289 Dyrk1b dual-specificity tyrosine phosphorylation regulated kinase 1b gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1316289 Dyrk1b dual-specificity tyrosine phosphorylation regulated kinase 1b gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1316289 Dyrk1b dual-specificity tyrosine phosphorylation regulated kinase 1b gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1316289 Dyrk1b dual-specificity tyrosine phosphorylation regulated kinase 1b gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1316289 Dyrk1b dual-specificity tyrosine phosphorylation regulated kinase 1b gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316289 Dyrk1b dual-specificity tyrosine phosphorylation regulated kinase 1b gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20200402 MGI 1316289 Dyrk1b dual-specificity tyrosine phosphorylation regulated kinase 1b gene MP:0012361 decreased large unstained cell number IEA N RGD:5509061 20170105 MGI 1316290 Fyb1 FYN binding protein 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11567141 1316290 Fyb1 FYN binding protein 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20231207 MGI 1316290 Fyb1 FYN binding protein 1 gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 1316290 Fyb1 FYN binding protein 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17646386 1316290 Fyb1 FYN binding protein 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:11567141 1316290 Fyb1 FYN binding protein 1 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:11567141 1316290 Fyb1 FYN binding protein 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11567141 1316290 Fyb1 FYN binding protein 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17646386 1316290 Fyb1 FYN binding protein 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:11567141 1316290 Fyb1 FYN binding protein 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17646386 1316290 Fyb1 FYN binding protein 1 gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20231207 MGI 1316291 Egfem1 EGF-like and EMI domain containing 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1316291 Egfem1 EGF-like and EMI domain containing 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1316291 Egfem1 EGF-like and EMI domain containing 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1316291 Egfem1 EGF-like and EMI domain containing 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1316291 Egfem1 EGF-like and EMI domain containing 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1316291 Egfem1 EGF-like and EMI domain containing 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1316291 Egfem1 EGF-like and EMI domain containing 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1316292 Tuba1c tubulin, alpha 1C gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 1316296 Raly hnRNP-associated with lethal yellow gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20181227 MGI 1316296 Raly hnRNP-associated with lethal yellow gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1316296 Raly hnRNP-associated with lethal yellow gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20181227 MGI 1316296 Raly hnRNP-associated with lethal yellow gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19168544 1316296 Raly hnRNP-associated with lethal yellow gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 1316299 Moap1 modulator of apoptosis 1 gene MP:0008891 decreased hepatocyte apoptosis IAGP N RGD:5509061 20180111 MGI PMID:27320914 1316304 Aebp2 AE binding protein 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:21949878 1316304 Aebp2 AE binding protein 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:21949878 1316304 Aebp2 AE binding protein 2 gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20141003 MGI PMID:21949878 1316304 Aebp2 AE binding protein 2 gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20141003 MGI PMID:21949878 1316304 Aebp2 AE binding protein 2 gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:21949878 1316304 Aebp2 AE binding protein 2 gene MP:0005175 non-pigmented tail tip IAGP N RGD:5509061 20141003 MGI PMID:21949878 1316304 Aebp2 AE binding protein 2 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:21949878 1316304 Aebp2 AE binding protein 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21949878 1316307 Relch RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1316307 Relch RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1316307 Relch RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20201022 MGI 1316307 Relch RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1316307 Relch RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1316307 Relch RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1316307 Relch RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1316307 Relch RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1316309 Lmod1 leiomodin 1 (smooth muscle) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1316311 Arhgap22 Rho GTPase activating protein 22 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20181227 MGI 1316311 Arhgap22 Rho GTPase activating protein 22 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 1316311 Arhgap22 Rho GTPase activating protein 22 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20201022 MGI 1316313 Nars1 asparaginyl-tRNA synthetase 1 gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20241010 MGI 1316313 Nars1 asparaginyl-tRNA synthetase 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241010 MGI 1316313 Nars1 asparaginyl-tRNA synthetase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20240627 MGI PMID:38495304 1316313 Nars1 asparaginyl-tRNA synthetase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1316313 Nars1 asparaginyl-tRNA synthetase 1 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241010 MGI 1316315 Dhx33 DEAH-box helicase 33 gene MP:0005477 increased circulating thyroxine level IEA N RGD:5509061 20211021 MGI 1316315 Dhx33 DEAH-box helicase 33 gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20210211 MGI PMID:32767810 1316315 Dhx33 DEAH-box helicase 33 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316315 Dhx33 DEAH-box helicase 33 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1316315 Dhx33 DEAH-box helicase 33 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0000160 kyphosis IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20211118 MGI PMID:27374329 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20170209 MGI PMID:14576056 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0000239 absent common myeloid progenitor cells IAGP N RGD:5509061 20170209 MGI PMID:14576056 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20211118 MGI PMID:27374329 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170209 MGI PMID:14576056 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20211118 MGI PMID:27374329 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0001304 cataract IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0001304 cataract IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0001304 cataract IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20211118 MGI PMID:27374329 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0001925 male infertility IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0001926 female infertility IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20170209 MGI PMID:14744753 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20170209 MGI PMID:14576056 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:14576056 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20211118 MGI PMID:27374329 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20170209 MGI PMID:14744753 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0003786 premature aging IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0003786 premature aging IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0004024 aneuploidy IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0004024 aneuploidy IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0004024 aneuploidy IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0004024 aneuploidy IAGP N RGD:5509061 20211118 MGI PMID:27374329 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0004025 polyploidy IAGP N RGD:5509061 20211118 MGI PMID:27374329 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20170209 MGI PMID:16476774 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20170209 MGI PMID:16476774 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20170209 MGI PMID:14576056 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0005150 cachexia IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20211118 MGI PMID:27374329 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0008007 abnormal cellular replicative senescence IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0008007 abnormal cellular replicative senescence IAGP N RGD:5509061 20170209 MGI PMID:16476774 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0009315 increased rectum adenocarcinoma incidence IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20170209 MGI PMID:14744753 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20211118 MGI PMID:27374329 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:14576056 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20211118 MGI PMID:27374329 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20170209 MGI PMID:23300461 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20170209 MGI PMID:23878276 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20201224 MGI PMID:31738183 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20170209 MGI PMID:14576056 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20211118 MGI PMID:27374329 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:15208629 1316317 Bub1b BUB1B, mitotic checkpoint serine/threonine kinase gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:23300461 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:18430026 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:18430026 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:17325035 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:22002997 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22002997 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:22002997 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:17325035 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17325035 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:17325035 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17325035 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:11017084 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:17325035 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22002997 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22002997 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22002997 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:11017084 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:17325035 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:17325035 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11027331 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17325035 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17325035 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:11017084 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11027331 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11027331 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22002997 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11017084 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11017084 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:18430026 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11027331 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:11027331 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11017084 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11027331 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17325035 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:18430026 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:18430026 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:18430026 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0004680 small xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:18430026 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:11017084 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11017084 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:22002997 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:22002997 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:22002997 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:22002997 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:22002997 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:22002997 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22002997 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11017084 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11027331 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11017084 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11027331 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18330926 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17325035 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0011200 abnormal extraembryonic coelom morphology IAGP N RGD:5509061 20141003 MGI PMID:11017084 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:11017084 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:17325035 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0012271 abnormal chordamesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11017084 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0012282 abnormal sternebra number IAGP N RGD:5509061 20141003 MGI PMID:18430026 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17325035 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0013505 decreased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17325035 1316320 Kat2a K(lysine) acetyltransferase 2A gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:22002997 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20240627 MGI PMID:33246328 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15472465 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18227763 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:9657845 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20240627 MGI PMID:33246328 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20240627 MGI PMID:33246328 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200402 MGI 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20240627 MGI PMID:33246328 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20240627 MGI PMID:33246328 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20240627 MGI PMID:33246328 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20240627 MGI PMID:33246328 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20240627 MGI PMID:33246328 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:15472465 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20240627 MGI PMID:33246328 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20240627 MGI PMID:33246328 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20240627 MGI PMID:33246328 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20240627 MGI PMID:33246328 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20240627 MGI PMID:33246328 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20240627 MGI PMID:33246328 1316322 Zc3h4 zinc finger CCCH-type containing 4 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240627 MGI 1316323 Slc25a44 solute carrier family 25, member 44 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210826 MGI 1316323 Slc25a44 solute carrier family 25, member 44 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1316323 Slc25a44 solute carrier family 25, member 44 gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20240307 MGI PMID:33944778 1316323 Slc25a44 solute carrier family 25, member 44 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20240307 MGI PMID:33944778 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15300255 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15485903 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:15300255 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210826 MGI 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:12904583 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:15485903 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15300255 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15485903 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15485903 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15485903 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12904583 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15300255 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:15485903 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15485903 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:15485903 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:15300255 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15485903 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15485903 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:15485903 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15485903 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0008762 embryonic lethality IEA N RGD:5509061 20141003 MGI 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15485903 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15300255 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20220519 MGI 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11431694 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15300255 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15485903 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15300255 1316327 Birc6 baculoviral IAP repeat-containing 6 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:15300255 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20230119 MGI 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20230119 MGI 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190207 MGI PMID:26880576 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20190207 MGI PMID:26880576 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0001488 increased startle reflex IEA N RGD:5509061 20231207 MGI 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20190207 MGI PMID:26880576 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0001924 infertility IAGP N RGD:5509061 20190207 MGI PMID:26880576 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20190207 MGI PMID:26880576 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0002938 white spotting IAGP N RGD:5509061 20190207 MGI PMID:26880576 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20190207 MGI PMID:26880576 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230119 MGI 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0005505 thrombocytosis IEA N RGD:5509061 20230119 MGI 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20190207 MGI PMID:26880576 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0008731 abnormal hair shaft melanin granule morphology IAGP N RGD:5509061 20190207 MGI PMID:26880576 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20190207 MGI PMID:26880576 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20190207 MGI PMID:26880576 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20230119 MGI 1316329 Rnaseh2a ribonuclease H2, large subunit gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:26880576 1316333 Hoxc10 homeobox C10 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:12869760 1316333 Hoxc10 homeobox C10 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316333 Hoxc10 homeobox C10 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316333 Hoxc10 homeobox C10 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1316333 Hoxc10 homeobox C10 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316333 Hoxc10 homeobox C10 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:12869760 1316333 Hoxc10 homeobox C10 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0003854 abnormal forelimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1316333 Hoxc10 homeobox C10 gene MP:0003856 abnormal hindlimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1316333 Hoxc10 homeobox C10 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:12869760 1316333 Hoxc10 homeobox C10 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:12869760 1316333 Hoxc10 homeobox C10 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0004614 caudal vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12869760 1316333 Hoxc10 homeobox C10 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12869760 1316333 Hoxc10 homeobox C10 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0004627 abnormal trochanter morphology IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0004654 absent lumbar vertebrae IAGP N RGD:5509061 20141003 MGI PMID:12869760 1316333 Hoxc10 homeobox C10 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0004694 absent patella IAGP N RGD:5509061 20141003 MGI PMID:12869760 1316333 Hoxc10 homeobox C10 gene MP:0006429 abnormal hyaline cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0010240 decreased skeletal muscle size IAGP N RGD:5509061 20141003 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0030774 abnormal ischiofemoral ligament morphology IAGP N RGD:5509061 20181004 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0030784 abnormal iliofemoral ligament morphology IAGP N RGD:5509061 20181004 MGI PMID:19623272 1316333 Hoxc10 homeobox C10 gene MP:0030830 abnormal acetabulum morphology IAGP N RGD:5509061 20181018 MGI PMID:19623272 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20180607 MGI PMID:24726366 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0001426 polydipsia IAGP N RGD:5509061 20180607 MGI PMID:24726366 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20180607 MGI PMID:24726366 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180607 MGI PMID:24726366 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180607 MGI PMID:24726366 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180607 MGI PMID:24726366 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20180607 MGI PMID:24726366 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20180607 MGI PMID:24726366 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20180607 MGI PMID:24726366 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20180531 MGI PMID:29082311 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20180531 MGI PMID:29082311 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20180531 MGI PMID:29082311 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20180531 MGI PMID:29082311 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20180531 MGI PMID:29082311 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20180531 MGI PMID:29082311 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180607 MGI PMID:24726366 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20180607 MGI PMID:24726366 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20180607 MGI PMID:24726366 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20180607 MGI PMID:24726366 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20180531 MGI PMID:29082311 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0013220 increased pancreas apoptosis IAGP N RGD:5509061 20180607 MGI PMID:24726366 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0013272 abnormal translation IAGP N RGD:5509061 20180531 MGI PMID:29082311 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0013272 abnormal translation IAGP N RGD:5509061 20180607 MGI PMID:24726366 1316337 Manf mesencephalic astrocyte-derived neurotrophic factor gene MP:0020599 increased cerebral cortex cell density IAGP N RGD:5509061 20180531 MGI PMID:29082311 1316339 Sav1 salvador family WW domain containing 1 gene MP:0000328 increased enterocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20404163 1316339 Sav1 salvador family WW domain containing 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:20404163 1316339 Sav1 salvador family WW domain containing 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20404163 1316339 Sav1 salvador family WW domain containing 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0001235 disorganized suprabasal layer IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0001329 retina hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20080689 1316339 Sav1 salvador family WW domain containing 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20404163 1316339 Sav1 salvador family WW domain containing 1 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20080689 1316339 Sav1 salvador family WW domain containing 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20404163 1316339 Sav1 salvador family WW domain containing 1 gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:21041407 1316339 Sav1 salvador family WW domain containing 1 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20160811 MGI PMID:26980762 1316339 Sav1 salvador family WW domain containing 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20080689 1316339 Sav1 salvador family WW domain containing 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20160811 MGI PMID:26980762 1316339 Sav1 salvador family WW domain containing 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20170223 MGI PMID:26131558 1316339 Sav1 salvador family WW domain containing 1 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20404163 1316339 Sav1 salvador family WW domain containing 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20080689 1316339 Sav1 salvador family WW domain containing 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20160811 MGI PMID:26980762 1316339 Sav1 salvador family WW domain containing 1 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:21041407 1316339 Sav1 salvador family WW domain containing 1 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:21041407 1316339 Sav1 salvador family WW domain containing 1 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20404163 1316339 Sav1 salvador family WW domain containing 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20080689 1316339 Sav1 salvador family WW domain containing 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20404163 1316339 Sav1 salvador family WW domain containing 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20160811 MGI PMID:26980762 1316339 Sav1 salvador family WW domain containing 1 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0008109 abnormal small intestinal microvillus morphology IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21041407 1316339 Sav1 salvador family WW domain containing 1 gene MP:0008992 abnormal portal lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:20404163 1316339 Sav1 salvador family WW domain containing 1 gene MP:0010040 abnormal oval cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20404163 1316339 Sav1 salvador family WW domain containing 1 gene MP:0010040 abnormal oval cell morphology IAGP N RGD:5509061 20160811 MGI PMID:26980762 1316339 Sav1 salvador family WW domain containing 1 gene MP:0010042 abnormal oval cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20404163 1316339 Sav1 salvador family WW domain containing 1 gene MP:0010054 increased hepatoblastoma incidence IAGP N RGD:5509061 20160811 MGI PMID:26980762 1316339 Sav1 salvador family WW domain containing 1 gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20404163 1316339 Sav1 salvador family WW domain containing 1 gene MP:0010802 abnormal intestinal enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0010945 lung epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20160811 MGI PMID:26980762 1316339 Sav1 salvador family WW domain containing 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18369314 1316339 Sav1 salvador family WW domain containing 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20404163 1316341 Gpalpp1 GPALPP motifs containing 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20230601 MGI 1316341 Gpalpp1 GPALPP motifs containing 1 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20230601 MGI 1316341 Gpalpp1 GPALPP motifs containing 1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20230601 MGI 1316343 Tbc1d31 TBC1 domain family, member 31 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1316343 Tbc1d31 TBC1 domain family, member 31 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1316347 Tmem67 transmembrane protein 67 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1316347 Tmem67 transmembrane protein 67 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0000829 dilated fourth ventricle IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0000923 abnormal roof plate morphology IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20230601 MGI 1316347 Tmem67 transmembrane protein 67 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21725307 1316347 Tmem67 transmembrane protein 67 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20160331 MGI PMID:21725307 1316347 Tmem67 transmembrane protein 67 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:21725307 1316347 Tmem67 transmembrane protein 67 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0003943 abnormal hepatobiliary system development IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 1316347 Tmem67 transmembrane protein 67 gene MP:0004157 interrupted aortic arch IEA N RGD:5509061 20141003 MGI 1316347 Tmem67 transmembrane protein 67 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0006100 abnormal tegmentum morphology IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0008282 enlarged hippocampus IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20141003 MGI 1316347 Tmem67 transmembrane protein 67 gene MP:0009689 abnormal neural tube ventricular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1316347 Tmem67 transmembrane protein 67 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1316347 Tmem67 transmembrane protein 67 gene MP:0010422 heart right ventricle hypoplasia IEA N RGD:5509061 20141003 MGI 1316347 Tmem67 transmembrane protein 67 gene MP:0010808 right-sided stomach IEA N RGD:5509061 20141003 MGI 1316347 Tmem67 transmembrane protein 67 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:21725307 1316347 Tmem67 transmembrane protein 67 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21725307 1316347 Tmem67 transmembrane protein 67 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21725307 1316347 Tmem67 transmembrane protein 67 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1316347 Tmem67 transmembrane protein 67 gene MP:0011253 situs inversus with levocardia IEA N RGD:5509061 20141003 MGI 1316347 Tmem67 transmembrane protein 67 gene MP:0011256 abnormal neural fold morphology IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0012139 increased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0012259 meningocele IAGP N RGD:5509061 20200910 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0012260 encephalomeningocele IAGP N RGD:5509061 20141003 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0012263 decreased hindbrain size IAGP N RGD:5509061 20171109 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0014278 semilobar holoprosencephaly IAGP N RGD:5509061 20230810 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0030309 abnormal posterior cranial fossa morphology IAGP N RGD:5509061 20171109 MGI PMID:23283079 1316347 Tmem67 transmembrane protein 67 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20230824 MGI PMID:23283079 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:14581464 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0000372 irregular coat pigmentation IEA N RGD:5509061 20150924 MGI 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:14581464 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:14581464 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0000420 ruffled hair IEA N RGD:5509061 20150924 MGI 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:14581464 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:14581464 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:14581464 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:14581464 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:14581464 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0001290 delayed eyelid opening IEA N RGD:5509061 20150924 MGI 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20150924 MGI 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0001511 disheveled coat IEA N RGD:5509061 20150924 MGI 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20150924 MGI 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:14581464 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0002991 abnormal sebaceous gland physiology IAGP N RGD:5509061 20141003 MGI PMID:14581464 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0002992 abnormal sebaceous lipid secretion IAGP N RGD:5509061 20141003 MGI PMID:14581464 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0003136 yellow coat color IEA N RGD:5509061 20150924 MGI 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0005072 abnormal hair follicle melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:14581464 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0011019 abnormal adaptive thermogenesis IAGP N RGD:5509061 20171228 MGI PMID:14581464 1316353 Elovl3 ELOVL fatty acid elongase 3 gene MP:0013146 eye lesions IEA N RGD:5509061 20150924 MGI 1316365 Lias lipoic acid synthetase gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:20450902 1316365 Lias lipoic acid synthetase gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20450902 1316365 Lias lipoic acid synthetase gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20450902 1316365 Lias lipoic acid synthetase gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15755804 1316365 Lias lipoic acid synthetase gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:20450902 1316365 Lias lipoic acid synthetase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16135825 1316365 Lias lipoic acid synthetase gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16135825 1316365 Lias lipoic acid synthetase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:20450902 1316365 Lias lipoic acid synthetase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20450902 1316365 Lias lipoic acid synthetase gene MP:0004387 abnormal prechordal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20450902 1316365 Lias lipoic acid synthetase gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:20450902 1316365 Lias lipoic acid synthetase gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16135825 1316365 Lias lipoic acid synthetase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 1316365 Lias lipoic acid synthetase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20450902 1316365 Lias lipoic acid synthetase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1316365 Lias lipoic acid synthetase gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:15755804 1316365 Lias lipoic acid synthetase gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:20450902 1316365 Lias lipoic acid synthetase gene MP:0012604 decreased glutathione level IAGP N RGD:5509061 20180920 MGI PMID:16135825 1316367 Epc2 enhancer of polycomb homolog 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1316367 Epc2 enhancer of polycomb homolog 2 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1316367 Epc2 enhancer of polycomb homolog 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1316367 Epc2 enhancer of polycomb homolog 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20201022 MGI 1316367 Epc2 enhancer of polycomb homolog 2 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20210826 MGI 1316367 Epc2 enhancer of polycomb homolog 2 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20160804 MGI 1316367 Epc2 enhancer of polycomb homolog 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210826 MGI 1316367 Epc2 enhancer of polycomb homolog 2 gene MP:0005571 decreased lactate dehydrogenase level IEA N RGD:5509061 20160804 MGI 1316367 Epc2 enhancer of polycomb homolog 2 gene MP:0005573 increased pulmonary respiratory rate IEA N RGD:5509061 20211021 MGI 1316367 Epc2 enhancer of polycomb homolog 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1316367 Epc2 enhancer of polycomb homolog 2 gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20210128 MGI 1316367 Epc2 enhancer of polycomb homolog 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316367 Epc2 enhancer of polycomb homolog 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:16598713 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20181115 MGI PMID:24769727 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16598713 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16598713 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:12522767 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16598713 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:16598713 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16598713 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:16162653 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:16162653 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:11857784 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16127714 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16598713 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:16127714 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12522767 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12522767 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16598713 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16598713 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16162653 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:16598713 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20181115 MGI PMID:24769727 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20181115 MGI PMID:24769727 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20181115 MGI PMID:24769727 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12522767 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16598713 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:16598713 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0006342 absent first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:12522767 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0008732 reduced hair shaft melanin granule number IAGP N RGD:5509061 20181115 MGI PMID:24769727 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0009759 abnormal hair follicle bulge morphology IAGP N RGD:5509061 20181115 MGI PMID:24769727 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20181115 MGI PMID:24769727 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0009784 abnormal melanoblast migration IAGP N RGD:5509061 20181115 MGI PMID:24769727 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16598713 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11857784 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12522767 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:16127714 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:16598713 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0012746 abnormal neural crest cell delamination IAGP N RGD:5509061 20141003 MGI PMID:12522767 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0012757 abnormal cranial neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:12522767 1316369 Zeb2 zinc finger E-box binding homeobox 2 gene MP:0013011 absent vagal neural crest cells IAGP N RGD:5509061 20141003 MGI PMID:12522767 1316371 Abcd4 ATP-binding cassette, sub-family D member 4 gene MP:0001413 abnormal response to new environment IEA N RGD:5509061 20141003 MGI 1316371 Abcd4 ATP-binding cassette, sub-family D member 4 gene MP:0005316 abnormal response to tactile stimuli IEA N RGD:5509061 20141003 MGI 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17668895 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:18690222 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17668895 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:18690222 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:18690222 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18690222 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0008644 increased circulating interleukin-12a level IAGP N RGD:5509061 20141003 MGI PMID:18690222 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:18690222 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0008666 increased interleukin-12a secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18690222 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:18690222 1316378 Rps6ka4 ribosomal protein S6 kinase, polypeptide 4 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18690222 1316382 Nkx6-2 NK6 homeobox 2 gene MP:0000909 abnormal facial motor nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18216204 1316382 Nkx6-2 NK6 homeobox 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15601927 1316382 Nkx6-2 NK6 homeobox 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:18216204 1316382 Nkx6-2 NK6 homeobox 2 gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16319924 1316382 Nkx6-2 NK6 homeobox 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15601927 1316382 Nkx6-2 NK6 homeobox 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15601927 1316382 Nkx6-2 NK6 homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11390667 1316382 Nkx6-2 NK6 homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11567614 1316382 Nkx6-2 NK6 homeobox 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:16319924 1316382 Nkx6-2 NK6 homeobox 2 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19363146 1316382 Nkx6-2 NK6 homeobox 2 gene MP:0004281 abnormal hypoglossal nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18216204 1316382 Nkx6-2 NK6 homeobox 2 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:15601927 1316382 Nkx6-2 NK6 homeobox 2 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:15601927 1316384 Sacs sacsin gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20181227 MGI 1316384 Sacs sacsin gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 1316384 Sacs sacsin gene MP:0000745 tremors IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0000747 muscle weakness IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20160128 MGI PMID:22307627 1316384 Sacs sacsin gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 1316384 Sacs sacsin gene MP:0001513 limb grasping IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0001525 impaired balance IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1316384 Sacs sacsin gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1316384 Sacs sacsin gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20190502 MGI 1316384 Sacs sacsin gene MP:0002637 small uterus IEA N RGD:5509061 20181227 MGI 1316384 Sacs sacsin gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0005405 axon degeneration IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20160128 MGI PMID:22307627 1316384 Sacs sacsin gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20160128 MGI PMID:22307627 1316384 Sacs sacsin gene MP:0009422 decreased gastrocnemius weight IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0009426 decreased soleus weight IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160304 MGI PMID:25260547 1316384 Sacs sacsin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 1316384 Sacs sacsin gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:25260547 1316386 Brd4 bromodomain containing 4 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20190502 MGI 1316386 Brd4 bromodomain containing 4 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0002764 short tibia IEA N RGD:5509061 20190502 MGI 1316386 Brd4 bromodomain containing 4 gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20191114 MGI PMID:30830987 1316386 Brd4 bromodomain containing 4 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1316386 Brd4 bromodomain containing 4 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1316386 Brd4 bromodomain containing 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1316386 Brd4 bromodomain containing 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1316386 Brd4 bromodomain containing 4 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1316386 Brd4 bromodomain containing 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11997514 1316386 Brd4 bromodomain containing 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316386 Brd4 bromodomain containing 4 gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20220811 MGI 1316386 Brd4 bromodomain containing 4 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1316386 Brd4 bromodomain containing 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1316390 Rrp1 ribosomal RNA processing 1 gene MP:0005534 decreased body temperature IEA N RGD:5509061 20220519 MGI 1316390 Rrp1 ribosomal RNA processing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316390 Rrp1 ribosomal RNA processing 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1316392 Sh2d3c SH2 domain containing 3C gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:20881139 1316392 Sh2d3c SH2 domain containing 3C gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20881139 1316392 Sh2d3c SH2 domain containing 3C gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:20881139 1316392 Sh2d3c SH2 domain containing 3C gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20881139 1316392 Sh2d3c SH2 domain containing 3C gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:20505138 1316392 Sh2d3c SH2 domain containing 3C gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20505138 1316392 Sh2d3c SH2 domain containing 3C gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20505138 1316392 Sh2d3c SH2 domain containing 3C gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:20505138 1316392 Sh2d3c SH2 domain containing 3C gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:20881139 1316392 Sh2d3c SH2 domain containing 3C gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:20881139 1316392 Sh2d3c SH2 domain containing 3C gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20881139 1316392 Sh2d3c SH2 domain containing 3C gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:20505138 1316392 Sh2d3c SH2 domain containing 3C gene MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20505138 1316392 Sh2d3c SH2 domain containing 3C gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20505138 1316392 Sh2d3c SH2 domain containing 3C gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:20505138 1316392 Sh2d3c SH2 domain containing 3C gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:20505138 1316392 Sh2d3c SH2 domain containing 3C gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20505138 1316392 Sh2d3c SH2 domain containing 3C gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:20603213 1316392 Sh2d3c SH2 domain containing 3C gene MP:0009946 abnormal olfactory bulb layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20881139 1316392 Sh2d3c SH2 domain containing 3C gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20881139 1316392 Sh2d3c SH2 domain containing 3C gene MP:0009951 abnormal olfactory bulb mitral cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20881139 1316392 Sh2d3c SH2 domain containing 3C gene MP:0010059 olfactory bulb hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20881139 1316392 Sh2d3c SH2 domain containing 3C gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20603213 1316392 Sh2d3c SH2 domain containing 3C gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20881139 1316397 Gcat glycine C-acetyltransferase (2-amino-3-ketobutyrate-coenzyme A ligase) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180503 MGI PMID:29323231 1316401 Ebag9 estrogen receptor-binding fragment-associated gene 9 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:19620783 1316401 Ebag9 estrogen receptor-binding fragment-associated gene 9 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19620783 1316401 Ebag9 estrogen receptor-binding fragment-associated gene 9 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19620783 1316401 Ebag9 estrogen receptor-binding fragment-associated gene 9 gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19620783 1316403 Osbpl11 oxysterol binding protein-like 11 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20210520 MGI 1316403 Osbpl11 oxysterol binding protein-like 11 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 1316403 Osbpl11 oxysterol binding protein-like 11 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1316403 Osbpl11 oxysterol binding protein-like 11 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316405 Rabgef1 RAB guanine nucleotide exchange factor (GEF) 1 gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15235600 1316405 Rabgef1 RAB guanine nucleotide exchange factor (GEF) 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15235600 1316405 Rabgef1 RAB guanine nucleotide exchange factor (GEF) 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15235600 1316405 Rabgef1 RAB guanine nucleotide exchange factor (GEF) 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15235600 1316405 Rabgef1 RAB guanine nucleotide exchange factor (GEF) 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15235600 1316405 Rabgef1 RAB guanine nucleotide exchange factor (GEF) 1 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:15235600 1316405 Rabgef1 RAB guanine nucleotide exchange factor (GEF) 1 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:15235600 1316405 Rabgef1 RAB guanine nucleotide exchange factor (GEF) 1 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15235600 1316405 Rabgef1 RAB guanine nucleotide exchange factor (GEF) 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15235600 1316405 Rabgef1 RAB guanine nucleotide exchange factor (GEF) 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:15235600 1316405 Rabgef1 RAB guanine nucleotide exchange factor (GEF) 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15235600 1316405 Rabgef1 RAB guanine nucleotide exchange factor (GEF) 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15235600 1316405 Rabgef1 RAB guanine nucleotide exchange factor (GEF) 1 gene MP:0030758 increased circulating histamine level IAGP N RGD:5509061 20180927 MGI PMID:15235600 1316405 Rabgef1 RAB guanine nucleotide exchange factor (GEF) 1 gene MP:0031395 cutaneous mastocytosis IAGP N RGD:5509061 20220721 MGI PMID:15235600 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0000435 shortened head IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0002649 abnormal enamel rod pattern IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0002764 short tibia IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0002772 brachypodia IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0003109 short femur IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0003742 narrow head IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0004351 short humerus IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0004355 short radius IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0004380 short frontal bone IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0004441 small occipital bone IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0010965 decreased compact bone volume IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316406 Slc10a7 solute carrier family 10 (sodium/bile acid cotransporter family), member 7 gene MP:0030245 round head IAGP N RGD:5509061 20181011 MGI PMID:30082715 1316410 Zic4 zinc finger protein of the cerebellum 4 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15338008 1316410 Zic4 zinc finger protein of the cerebellum 4 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:15338008 1316410 Zic4 zinc finger protein of the cerebellum 4 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:15338008 1316410 Zic4 zinc finger protein of the cerebellum 4 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15338008 1316410 Zic4 zinc finger protein of the cerebellum 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15338008 1316410 Zic4 zinc finger protein of the cerebellum 4 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15338008 1316410 Zic4 zinc finger protein of the cerebellum 4 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:15338008 1316410 Zic4 zinc finger protein of the cerebellum 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15338008 1316412 Wasf2 WASP family, member 2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20200514 MGI 1316412 Wasf2 WASP family, member 2 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12853475 1316412 Wasf2 WASP family, member 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:12853475 1316412 Wasf2 WASP family, member 2 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12853475 1316412 Wasf2 WASP family, member 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12853475 1316412 Wasf2 WASP family, member 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12853475 1316412 Wasf2 WASP family, member 2 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0003542 abnormal vascular endothelial cell development IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210128 MGI 1316412 Wasf2 WASP family, member 2 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12853475 1316412 Wasf2 WASP family, member 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12853475 1316412 Wasf2 WASP family, member 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1316412 Wasf2 WASP family, member 2 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0020327 abnormal capillary branching pattern IAGP N RGD:5509061 20160714 MGI PMID:12879075 1316412 Wasf2 WASP family, member 2 gene MP:0020329 decreased capillary density IAGP N RGD:5509061 20160714 MGI PMID:12879075 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:16284304 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16284304 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000738 impaired muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000747 muscle weakness IAGP N RGD:5509061 20160304 MGI PMID:25564733 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000747 muscle weakness IAGP N RGD:5509061 20240516 MGI PMID:30689883 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000747 muscle weakness IAGP N RGD:5509061 20240516 MGI PMID:31044239 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000751 myopathy IAGP N RGD:5509061 20160304 MGI PMID:25564733 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:11818962 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16284304 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21803290 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11818962 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11818962 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20240516 MGI PMID:30689883 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20240516 MGI PMID:31044239 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:7515481 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:7515481 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16284304 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20210422 MGI PMID:30236258 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20220421 MGI PMID:34257294 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16284304 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:7515481 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0002083 premature death IAGP N RGD:5509061 20210422 MGI PMID:30236258 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:16284304 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21803290 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:22139840 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:23070698 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20210422 MGI PMID:30236258 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20220421 MGI PMID:34257294 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:7515481 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:7515481 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0002318 hypercapnia IAGP N RGD:5509061 20141003 MGI PMID:17122579 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:7515481 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0003030 acidemia IAGP N RGD:5509061 20141003 MGI PMID:17122579 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0003030 acidemia IAGP N RGD:5509061 20141003 MGI PMID:22139840 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:16284304 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20141003 MGI PMID:22139840 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16284304 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23070698 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:7515481 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20160304 MGI PMID:25564733 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20240516 MGI PMID:31044239 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:22139840 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004032 abnormal interventricular groove morphology IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20240516 MGI PMID:32242214 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20160304 MGI PMID:25564733 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20160304 MGI PMID:25564733 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20160304 MGI PMID:25564733 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21289290 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:7515481 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17122579 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20240516 MGI PMID:30689883 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20240516 MGI PMID:31044239 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20240516 MGI PMID:32242214 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004674 thin ribs IAGP N RGD:5509061 20141003 MGI PMID:11818962 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0004952 increased spleen weight IEA N RGD:5509061 20181227 MGI 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0005247 abnormal extraocular muscle morphology IAGP N RGD:5509061 20240516 MGI PMID:32242214 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0005369 muscle phenotype IAGP N RGD:5509061 20240516 MGI PMID:32242214 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20240516 MGI PMID:31044239 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0005380 embryo phenotype IAGP N RGD:5509061 20240516 MGI PMID:31044239 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0005391 vision/eye phenotype IAGP N RGD:5509061 20240516 MGI PMID:32242214 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:17122579 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16284304 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21289290 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21803290 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9054435 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:16284304 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20160304 MGI PMID:25564733 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20160304 MGI PMID:25564733 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20240516 MGI PMID:31044239 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22139840 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20210422 MGI PMID:30236258 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20220421 MGI PMID:34257294 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009045 muscle tetany IAGP N RGD:5509061 20141003 MGI PMID:21289290 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009046 muscle twitch IAGP N RGD:5509061 20141003 MGI PMID:21289290 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:7515481 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:16284304 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:7515481 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:7515481 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20160304 MGI PMID:25564733 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:7515481 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009411 abnormal skeletal muscle fiber triad morphology IAGP N RGD:5509061 20240516 MGI PMID:30689883 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009411 abnormal skeletal muscle fiber triad morphology IAGP N RGD:5509061 20240516 MGI PMID:31044239 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20240516 MGI PMID:30689883 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20240516 MGI PMID:31044239 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16284304 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210422 MGI PMID:30236258 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17122579 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19959667 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23070698 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160304 MGI PMID:25564733 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:16284304 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20240516 MGI PMID:31044239 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20210128 MGI 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0010405 ostium secundum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0011016 increased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:22139840 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7515481 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16284304 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17122579 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20220421 MGI PMID:34257294 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20160304 MGI PMID:25564733 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0011978 abnormal potassium ion homeostasis IAGP N RGD:5509061 20160304 MGI PMID:25564733 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:18003898 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0012514 pectus excavatum IAGP N RGD:5509061 20141003 MGI PMID:16284304 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0014344 abnormal skeletal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240516 MGI PMID:31044239 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0020214 increased susceptibility to malignant hyperthermia IAGP N RGD:5509061 20141003 MGI PMID:17122579 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0020214 increased susceptibility to malignant hyperthermia IAGP N RGD:5509061 20141003 MGI PMID:22139840 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0020214 increased susceptibility to malignant hyperthermia IAGP N RGD:5509061 20210422 MGI PMID:30236258 1316414 Ryr1 ryanodine receptor 1, skeletal muscle gene MP:0020214 increased susceptibility to malignant hyperthermia IAGP N RGD:5509061 20220421 MGI PMID:34257294 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:21303696 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:21303696 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:21303696 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:15082788 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:21303696 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20221110 MGI PMID:35708320 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0000958 peripheral nervous system degeneration IAGP N RGD:5509061 20141003 MGI PMID:15082788 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20221110 MGI PMID:35708320 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21303696 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:21303696 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20221110 MGI PMID:35708320 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20221110 MGI PMID:35708320 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20221110 MGI PMID:35708320 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15082788 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:21303696 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20231207 MGI 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20221110 MGI PMID:35708320 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21303696 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20221110 MGI PMID:35708320 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20221110 MGI PMID:35708320 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20221110 MGI PMID:35708320 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:21303696 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20221110 MGI PMID:35708320 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:21303696 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:15082788 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20221110 MGI PMID:35708320 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1316420 Ndrg1 N-myc downstream regulated gene 1 gene MP:0031204 hindlimb paresis IAGP N RGD:5509061 20221110 MGI PMID:35708320 1316425 Ndufa9 NADH:ubiquinone oxidoreductase subunit A9 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191205 MGI 1316425 Ndufa9 NADH:ubiquinone oxidoreductase subunit A9 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1316425 Ndufa9 NADH:ubiquinone oxidoreductase subunit A9 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191205 MGI 1316425 Ndufa9 NADH:ubiquinone oxidoreductase subunit A9 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1316425 Ndufa9 NADH:ubiquinone oxidoreductase subunit A9 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191205 MGI 1316425 Ndufa9 NADH:ubiquinone oxidoreductase subunit A9 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191205 MGI 1316425 Ndufa9 NADH:ubiquinone oxidoreductase subunit A9 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1316425 Ndufa9 NADH:ubiquinone oxidoreductase subunit A9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316425 Ndufa9 NADH:ubiquinone oxidoreductase subunit A9 gene MP:0012724 absent head fold IEA N RGD:5509061 20191205 MGI 1316425 Ndufa9 NADH:ubiquinone oxidoreductase subunit A9 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20190502 MGI 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:21725297 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22340501 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:11714751 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11714751 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12515813 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11714751 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22340501 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11714751 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12515813 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11485735 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11714751 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:11485735 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:11485735 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:11714751 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11714751 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11714751 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11714751 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:12515813 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11714751 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12515813 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:11714751 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12515813 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:12515813 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:12515813 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11714751 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:11485735 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:11485735 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:11714751 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:11485735 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:11714751 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:11485735 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:21725297 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0010205 abnormal oligodendrocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21725297 1316427 Tnfrsf21 tumor necrosis factor receptor superfamily, member 21 gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:22340501 1316434 Ppp4r2 protein phosphatase 4, regulatory subunit 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1316434 Ppp4r2 protein phosphatase 4, regulatory subunit 2 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 1316434 Ppp4r2 protein phosphatase 4, regulatory subunit 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20161201 MGI 1316434 Ppp4r2 protein phosphatase 4, regulatory subunit 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:21228006 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:17127040 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20180118 MGI PMID:21228006 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:18505822 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0000568 ectopic digits IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:21228006 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:17127040 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17127040 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0001678 thick apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:18257070 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:18257070 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:21228006 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0002902 decreased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0002963 decreased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0003870 decreased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:21228006 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17481602 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0004539 absent maxilla IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0006293 absent nasal placodes IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0006294 absent optic vesicle IAGP N RGD:5509061 20141003 MGI PMID:17127040 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:17127040 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:18505822 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0010939 abnormal mandibular prominence morphology IAGP N RGD:5509061 20171109 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17133501 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21228006 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0011496 abnormal head size IAGP N RGD:5509061 20141003 MGI PMID:21228006 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0011843 abnormal kidney collecting duct epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0011858 elongated kidney papilla IAGP N RGD:5509061 20141003 MGI PMID:21354128 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:17127040 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:21228006 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0012178 absent frontonasal prominence IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0012182 abnormal presomitic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18257070 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0012517 absent diencephalon IAGP N RGD:5509061 20141003 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0030324 abnormal anterior head development IAGP N RGD:5509061 20171109 MGI PMID:11702953 1316436 Dkk1 dickkopf WNT signaling pathway inhibitor 1 gene MP:0030324 abnormal anterior head development IAGP N RGD:5509061 20180118 MGI PMID:17133501 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20201022 MGI 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20180208 MGI PMID:29078349 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0000416 sparse hair IAGP N RGD:5509061 20180208 MGI PMID:29078349 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0001190 reddish skin IAGP N RGD:5509061 20180208 MGI PMID:29078349 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20180208 MGI PMID:29078349 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20180208 MGI PMID:29078349 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20180208 MGI PMID:29078349 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20180208 MGI PMID:29078349 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20180208 MGI PMID:29078349 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20180208 MGI PMID:29078349 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20180208 MGI PMID:25074913 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20180208 MGI PMID:29078349 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180208 MGI PMID:25074913 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20180208 MGI PMID:25074913 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20180208 MGI PMID:29078349 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0009598 thin epidermis stratum granulosum IAGP N RGD:5509061 20180208 MGI PMID:29078349 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180208 MGI PMID:29078349 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0011687 decreased epidermal stem cell number IAGP N RGD:5509061 20180208 MGI PMID:29078349 1316446 Slc39a10 solute carrier family 39 (zinc transporter), member 10 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1316448 Scai suppressor of cancer cell invasion gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20170615 MGI PMID:27820601 1316448 Scai suppressor of cancer cell invasion gene MP:0001147 small testis IAGP N RGD:5509061 20170615 MGI PMID:27820601 1316448 Scai suppressor of cancer cell invasion gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20170615 MGI PMID:27820601 1316448 Scai suppressor of cancer cell invasion gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20170615 MGI PMID:27820601 1316448 Scai suppressor of cancer cell invasion gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20170615 MGI PMID:27820601 1316448 Scai suppressor of cancer cell invasion gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20170615 MGI PMID:27820601 1316448 Scai suppressor of cancer cell invasion gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20170615 MGI PMID:27820601 1316448 Scai suppressor of cancer cell invasion gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20170615 MGI PMID:27820601 1316448 Scai suppressor of cancer cell invasion gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20170615 MGI PMID:27820601 1316448 Scai suppressor of cancer cell invasion gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:27820601 1316450 Adamts12 ADAM metallopeptidase with thrombospondin type 1 motif 12 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1316450 Adamts12 ADAM metallopeptidase with thrombospondin type 1 motif 12 gene MP:0001148 enlarged testis IEA N RGD:5509061 20210826 MGI 1316450 Adamts12 ADAM metallopeptidase with thrombospondin type 1 motif 12 gene MP:0001304 cataract IEA N RGD:5509061 20210826 MGI 1316450 Adamts12 ADAM metallopeptidase with thrombospondin type 1 motif 12 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1316450 Adamts12 ADAM metallopeptidase with thrombospondin type 1 motif 12 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20208563 1316450 Adamts12 ADAM metallopeptidase with thrombospondin type 1 motif 12 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20208563 1316450 Adamts12 ADAM metallopeptidase with thrombospondin type 1 motif 12 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:20208563 1316451 Katnip katanin interacting protein gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210128 MGI 1316451 Katnip katanin interacting protein gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20170504 MGI PMID:26714646 1316451 Katnip katanin interacting protein gene MP:0000917 obstructive hydrocephaly IAGP N RGD:5509061 20170504 MGI PMID:26714646 1316451 Katnip katanin interacting protein gene MP:0001304 cataract IEA N RGD:5509061 20210826 MGI 1316451 Katnip katanin interacting protein gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1316451 Katnip katanin interacting protein gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1316451 Katnip katanin interacting protein gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1316451 Katnip katanin interacting protein gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20170504 MGI PMID:26714646 1316451 Katnip katanin interacting protein gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1316451 Katnip katanin interacting protein gene MP:0002958 cerebral aqueductal stenosis IAGP N RGD:5509061 20170504 MGI PMID:26714646 1316451 Katnip katanin interacting protein gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 1316451 Katnip katanin interacting protein gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20170504 MGI PMID:26714646 1316451 Katnip katanin interacting protein gene MP:0013907 abnormal cerebrospinal fluid flow IAGP N RGD:5509061 20170504 MGI PMID:26714646 1316459 Trim7 tripartite motif-containing 7 gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20201224 MGI PMID:32126128 1316459 Trim7 tripartite motif-containing 7 gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20201224 MGI PMID:32126128 1316461 Gle1 GLE1 RNA export mediator gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1316461 Gle1 GLE1 RNA export mediator gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:7595654 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000753 paralysis IAGP N RGD:5509061 20180802 MGI PMID:29437892 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:7595654 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17571074 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:17571074 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17571074 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:17571074 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20180802 MGI PMID:29437892 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:7595654 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20180802 MGI PMID:29437892 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20180802 MGI PMID:29437892 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0000958 peripheral nervous system degeneration IEA N RGD:5509061 20111116 MGI 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:7595654 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:7595654 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0001255 decreased body height IAGP N RGD:5509061 20180802 MGI PMID:29437892 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0001265 decreased body size IAGP N RGD:5509061 20180802 MGI PMID:29437892 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17571074 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:7595654 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0001391 abnormal tail movements IAGP N RGD:5509061 20141003 MGI PMID:7595654 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20111215 MGI 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0001393 ataxia IEA N RGD:5509061 20190530 MGI 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0001405 impaired coordination IEA N RGD:5509061 20190530 MGI 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180802 MGI PMID:29437892 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0001921 reduced fertility IEA N RGD:5509061 20111116 MGI 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0002183 gliosis IAGP N RGD:5509061 20180802 MGI PMID:29437892 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:7595654 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:7595654 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20180802 MGI PMID:29437892 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0002752 abnormal somatic nervous system morphology IEA N RGD:5509061 20111116 MGI 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0003492 abnormal involuntary movement IEA N RGD:5509061 20111116 MGI 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0003633 abnormal nervous system physiology IEA N RGD:5509061 20111116 MGI 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:17571074 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:7595654 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:7595654 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0004220 abnormal peripheral nervous system regeneration IEA N RGD:5509061 20111116 MGI 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0004243 abnormal motor nerve collateral sprouting IAGP N RGD:5509061 20141003 MGI PMID:7595654 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7595654 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0004819 decreased skeletal muscle mass IEA N RGD:5509061 20111116 MGI 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:17571074 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:17571074 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20180802 MGI PMID:29437892 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:7595654 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20180802 MGI PMID:29437892 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23175812 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:7595654 1316463 Scyl1 SCY1-like 1 (S. cerevisiae) gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20180802 MGI PMID:29437892 1316468 Abca8a ATP-binding cassette, sub-family A member 8a gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20240523 MGI 1316468 Abca8a ATP-binding cassette, sub-family A member 8a gene MP:0002608 increased hematocrit IEA N RGD:5509061 20230601 MGI 1316468 Abca8a ATP-binding cassette, sub-family A member 8a gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20637190 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:20637190 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20170105 MGI PMID:27297885 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20170105 MGI PMID:27297885 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:20637190 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20170105 MGI PMID:27297885 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0003543 abnormal vascular endothelial cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20637190 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:20637190 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0003954 abnormal Reichert's membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:20637190 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:20637190 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20170105 MGI PMID:27297885 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20637190 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0008533 abnormal anterior visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:20637190 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0008533 abnormal anterior visceral endoderm morphology IAGP N RGD:5509061 20170105 MGI PMID:27297885 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20161229 MGI PMID:27297885 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20637190 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:20637190 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:20637190 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20637190 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20637190 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170105 MGI PMID:27297885 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20170105 MGI PMID:27297885 1316470 Pofut2 protein O-fucosyltransferase 2 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20170105 MGI PMID:27297885 1316475 Wdfy2 WD repeat and FYVE domain containing 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20210513 MGI PMID:32641353 1316475 Wdfy2 WD repeat and FYVE domain containing 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20210513 MGI PMID:32641353 1316475 Wdfy2 WD repeat and FYVE domain containing 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20210513 MGI PMID:32641353 1316475 Wdfy2 WD repeat and FYVE domain containing 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20210513 MGI PMID:32641353 1316475 Wdfy2 WD repeat and FYVE domain containing 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20210513 MGI PMID:32641353 1316475 Wdfy2 WD repeat and FYVE domain containing 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210513 MGI PMID:32641353 1316475 Wdfy2 WD repeat and FYVE domain containing 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20210513 MGI PMID:32641353 1316475 Wdfy2 WD repeat and FYVE domain containing 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20210513 MGI PMID:32641353 1316475 Wdfy2 WD repeat and FYVE domain containing 2 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20210513 MGI PMID:32641353 1316475 Wdfy2 WD repeat and FYVE domain containing 2 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20210513 MGI PMID:32641353 1316475 Wdfy2 WD repeat and FYVE domain containing 2 gene MP:0020102 increased hepatic glucose production IAGP N RGD:5509061 20210513 MGI PMID:32641353 1316477 Igdcc3 immunoglobulin superfamily, DCC subclass, member 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11486040 1316479 Trim33 tripartite motif-containing 33 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20240523 MGI 1316479 Trim33 tripartite motif-containing 33 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1316479 Trim33 tripartite motif-containing 33 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0001314 cornea opacity IEA N RGD:5509061 20220519 MGI 1316479 Trim33 tripartite motif-containing 33 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:19629168 1316479 Trim33 tripartite motif-containing 33 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:19629168 1316479 Trim33 tripartite motif-containing 33 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18543301 1316479 Trim33 tripartite motif-containing 33 gene MP:0002583 absent extraembryonic ectoderm IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:19629168 1316479 Trim33 tripartite motif-containing 33 gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18543301 1316479 Trim33 tripartite motif-containing 33 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0008533 abnormal anterior visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0009110 pancreas hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19629168 1316479 Trim33 tripartite motif-containing 33 gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:19629168 1316479 Trim33 tripartite motif-containing 33 gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:19629168 1316479 Trim33 tripartite motif-containing 33 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19629168 1316479 Trim33 tripartite motif-containing 33 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19629168 1316479 Trim33 tripartite motif-containing 33 gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18543301 1316479 Trim33 tripartite motif-containing 33 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1316479 Trim33 tripartite motif-containing 33 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0011197 abnormal proamniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0012159 absent anterior visceral endoderm IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0012160 expanded anterior visceral endoderm IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316479 Trim33 tripartite motif-containing 33 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:20573697 1316481 Ptpn4 protein tyrosine phosphatase, non-receptor type 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170209 MGI PMID:17953619 1316481 Ptpn4 protein tyrosine phosphatase, non-receptor type 4 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20170209 MGI PMID:17953619 1316481 Ptpn4 protein tyrosine phosphatase, non-receptor type 4 gene MP:0002807 abnormal eye blink conditioning behavior IAGP N RGD:5509061 20170209 MGI PMID:17953619 1316483 Capn12 calpain 12 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1316483 Capn12 calpain 12 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1316483 Capn12 calpain 12 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1316483 Capn12 calpain 12 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1316483 Capn12 calpain 12 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1316483 Capn12 calpain 12 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20181227 MGI 1316483 Capn12 calpain 12 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1316483 Capn12 calpain 12 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 1316486 Herpud2 HERPUD family member 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1316489 Zfp521 zinc finger protein 521 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20951345 1316489 Zfp521 zinc finger protein 521 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21642473 1316489 Zfp521 zinc finger protein 521 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0002083 premature death IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20951345 1316489 Zfp521 zinc finger protein 521 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20951345 1316489 Zfp521 zinc finger protein 521 gene MP:0003063 increased coping response IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:20951345 1316489 Zfp521 zinc finger protein 521 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:20951345 1316489 Zfp521 zinc finger protein 521 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:20951345 1316489 Zfp521 zinc finger protein 521 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21173110 1316489 Zfp521 zinc finger protein 521 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:20951345 1316489 Zfp521 zinc finger protein 521 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:20951345 1316489 Zfp521 zinc finger protein 521 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:21642473 1316489 Zfp521 zinc finger protein 521 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:21173110 1316489 Zfp521 zinc finger protein 521 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:20951345 1316489 Zfp521 zinc finger protein 521 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0008938 decreased pituitary gland weight IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:20951345 1316489 Zfp521 zinc finger protein 521 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0009393 abnormal resting posture IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20951345 1316489 Zfp521 zinc finger protein 521 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21642473 1316489 Zfp521 zinc finger protein 521 gene MP:0009911 increased hyoid bone size IAGP N RGD:5509061 20141003 MGI PMID:21173110 1316489 Zfp521 zinc finger protein 521 gene MP:0009912 decreased hyoid bone size IAGP N RGD:5509061 20141003 MGI PMID:21173110 1316489 Zfp521 zinc finger protein 521 gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:20951345 1316489 Zfp521 zinc finger protein 521 gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0012204 abnormal neuronal stem cell physiology IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0013308 decreased adrenal gland weight IAGP N RGD:5509061 20151231 MGI PMID:24676388 1316489 Zfp521 zinc finger protein 521 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:24676388 1316491 Fbxo21 F-box protein 21 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20190502 MGI 1316491 Fbxo21 F-box protein 21 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1316491 Fbxo21 F-box protein 21 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20230330 MGI PMID:35987460 1316491 Fbxo21 F-box protein 21 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20230330 MGI PMID:35987460 1316491 Fbxo21 F-box protein 21 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20230330 MGI PMID:35987460 1316491 Fbxo21 F-box protein 21 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20230330 MGI PMID:35987460 1316491 Fbxo21 F-box protein 21 gene MP:0013696 increased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20230330 MGI PMID:35987460 1316491 Fbxo21 F-box protein 21 gene MP:0031276 abnormal stress erythropoiesis IAGP N RGD:5509061 20230330 MGI PMID:35987460 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20221215 MGI 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0009233 enlarged sperm head IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0009839 multiflagellated sperm IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0013538 increased Harderian gland adenoma incidence IAGP N RGD:5509061 20150219 MGI PMID:21124965 1316493 Ing2 inhibitor of growth family, member 2 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:21124965 1316495 Nhlrc2 NHL repeat containing 2 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20220519 MGI PMID:35258166 1316495 Nhlrc2 NHL repeat containing 2 gene MP:0003087 absent allantois IAGP N RGD:5509061 20220519 MGI PMID:35258166 1316495 Nhlrc2 NHL repeat containing 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20220519 MGI PMID:35258166 1316495 Nhlrc2 NHL repeat containing 2 gene MP:0005030 absent amnion IAGP N RGD:5509061 20220519 MGI PMID:35258166 1316495 Nhlrc2 NHL repeat containing 2 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1316495 Nhlrc2 NHL repeat containing 2 gene MP:0009593 absent chorion IAGP N RGD:5509061 20220519 MGI PMID:35258166 1316495 Nhlrc2 NHL repeat containing 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1316495 Nhlrc2 NHL repeat containing 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20220519 MGI PMID:35258166 1316495 Nhlrc2 NHL repeat containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316495 Nhlrc2 NHL repeat containing 2 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20220519 MGI PMID:35258166 1316496 Yju2 YJU2 splicing factor gene MP:0000745 tremors IEA N RGD:5509061 20201231 MGI 1316496 Yju2 YJU2 splicing factor gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1316496 Yju2 YJU2 splicing factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316496 Yju2 YJU2 splicing factor gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1316498 Glipr2 GLI pathogenesis-related 2 gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20211216 MGI PMID:33222586 1316499 Oasl2 2'-5' oligoadenylate synthetase-like 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160804 MGI 1316508 Tent4a terminal nucleotidyltransferase 4A gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20210826 MGI 1316508 Tent4a terminal nucleotidyltransferase 4A gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200514 MGI 1316508 Tent4a terminal nucleotidyltransferase 4A gene MP:0001147 small testis IEA N RGD:5509061 20200514 MGI 1316508 Tent4a terminal nucleotidyltransferase 4A gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1316508 Tent4a terminal nucleotidyltransferase 4A gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1316508 Tent4a terminal nucleotidyltransferase 4A gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1316508 Tent4a terminal nucleotidyltransferase 4A gene MP:0003036 vertebral transformation IEA N RGD:5509061 20210826 MGI 1316508 Tent4a terminal nucleotidyltransferase 4A gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20210826 MGI 1316508 Tent4a terminal nucleotidyltransferase 4A gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20200514 MGI 1316508 Tent4a terminal nucleotidyltransferase 4A gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20200514 MGI 1316509 Enkd1 enkurin domain containing 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1316509 Enkd1 enkurin domain containing 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1316509 Enkd1 enkurin domain containing 1 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20220825 MGI PMID:35301795 1316509 Enkd1 enkurin domain containing 1 gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20220825 MGI PMID:35301795 1316509 Enkd1 enkurin domain containing 1 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20220825 MGI PMID:35301795 1316509 Enkd1 enkurin domain containing 1 gene MP:0010393 shortened QRS complex duration IAGP N RGD:5509061 20220825 MGI PMID:35301795 1316509 Enkd1 enkurin domain containing 1 gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20220825 MGI PMID:35301795 1316509 Enkd1 enkurin domain containing 1 gene MP:0011065 abnormal kidney epithelial cell primary cilium morphology IAGP N RGD:5509061 20220825 MGI PMID:35301795 1316509 Enkd1 enkurin domain containing 1 gene MP:0011919 abnormal R wave IAGP N RGD:5509061 20220825 MGI PMID:35301795 1316509 Enkd1 enkurin domain containing 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20220825 MGI PMID:35301795 1316509 Enkd1 enkurin domain containing 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20220825 MGI PMID:35301795 1316509 Enkd1 enkurin domain containing 1 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20220825 MGI PMID:35301795 1316509 Enkd1 enkurin domain containing 1 gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20220825 MGI PMID:35301795 1316510 Lrrc10 leucine rich repeat containing 10 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170803 MGI PMID:23236519 1316510 Lrrc10 leucine rich repeat containing 10 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170803 MGI PMID:23236519 1316510 Lrrc10 leucine rich repeat containing 10 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20170803 MGI PMID:23236519 1316510 Lrrc10 leucine rich repeat containing 10 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20170803 MGI PMID:23236519 1316510 Lrrc10 leucine rich repeat containing 10 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170803 MGI PMID:23236519 1316510 Lrrc10 leucine rich repeat containing 10 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170803 MGI PMID:23236519 1316510 Lrrc10 leucine rich repeat containing 10 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1316512 Brd9 bromodomain containing 9 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1316512 Brd9 bromodomain containing 9 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1316512 Brd9 bromodomain containing 9 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1316512 Brd9 bromodomain containing 9 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1316512 Brd9 bromodomain containing 9 gene MP:0002637 small uterus IEA N RGD:5509061 20210826 MGI 1316512 Brd9 bromodomain containing 9 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20210826 MGI 1316512 Brd9 bromodomain containing 9 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1316512 Brd9 bromodomain containing 9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1316512 Brd9 bromodomain containing 9 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210826 MGI 1316514 Atf1 activating transcription factor 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11865068 1316514 Atf1 activating transcription factor 1 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:11865068 1316514 Atf1 activating transcription factor 1 gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20141003 MGI PMID:11865068 1316514 Atf1 activating transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11865068 1316514 Atf1 activating transcription factor 1 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:11865068 1316514 Atf1 activating transcription factor 1 gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:11865068 1316514 Atf1 activating transcription factor 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17376811 1316514 Atf1 activating transcription factor 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:11865068 1316514 Atf1 activating transcription factor 1 gene MP:0003695 delayed blastocyst hatching from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:11865068 1316514 Atf1 activating transcription factor 1 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:11865068 1316514 Atf1 activating transcription factor 1 gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:11865068 1316514 Atf1 activating transcription factor 1 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:11865068 1316514 Atf1 activating transcription factor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11865068 1316514 Atf1 activating transcription factor 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11865068 1316515 Bcl2l12 BCL2 like 12 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20181227 MGI 1316515 Bcl2l12 BCL2 like 12 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 1316515 Bcl2l12 BCL2 like 12 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20181227 MGI 1316515 Bcl2l12 BCL2 like 12 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20210128 MGI 1316515 Bcl2l12 BCL2 like 12 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1316515 Bcl2l12 BCL2 like 12 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1316517 Bccip BRCA2 and CDKN1A interacting protein gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1316517 Bccip BRCA2 and CDKN1A interacting protein gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1316517 Bccip BRCA2 and CDKN1A interacting protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316521 Spata13 spermatogenesis associated 13 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:19893577 1316521 Spata13 spermatogenesis associated 13 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20190613 MGI PMID:31020388 1316521 Spata13 spermatogenesis associated 13 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20190613 MGI PMID:31020388 1316521 Spata13 spermatogenesis associated 13 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20170413 MGI PMID:19893577 1316521 Spata13 spermatogenesis associated 13 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20190613 MGI PMID:31020388 1316521 Spata13 spermatogenesis associated 13 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20170413 MGI PMID:19893577 1316521 Spata13 spermatogenesis associated 13 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20170413 MGI PMID:19893577 1316521 Spata13 spermatogenesis associated 13 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20170413 MGI PMID:19893577 1316521 Spata13 spermatogenesis associated 13 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20170413 MGI PMID:19893577 1316521 Spata13 spermatogenesis associated 13 gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20170413 MGI PMID:19893577 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20221103 MGI PMID:34211969 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221103 MGI PMID:34211969 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20221215 MGI 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20221103 MGI PMID:34211969 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19004860 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20221103 MGI PMID:34211969 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19004860 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20221103 MGI PMID:34211969 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19004860 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220519 MGI 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200514 MGI 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:19004860 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:19004860 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:19004860 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20221103 MGI PMID:34211969 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20221103 MGI PMID:34211969 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20221103 MGI PMID:34211969 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:19004860 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:19004860 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0004203 abnormal cranial flexure morphology IAGP N RGD:5509061 20141003 MGI PMID:19004860 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0004203 abnormal cranial flexure morphology IAGP N RGD:5509061 20221103 MGI PMID:34211969 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:19004860 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20221215 MGI 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20221103 MGI PMID:34211969 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19004860 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20221103 MGI PMID:34211969 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200514 MGI 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20221103 MGI PMID:34211969 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0013208 abnormal cilium physiology IAGP N RGD:5509061 20221103 MGI PMID:34211969 1316524 C2cd3 C2 calcium-dependent domain containing 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1316526 Zbtb5 zinc finger and BTB domain containing 5 gene MP:0001293 anophthalmia IEA N RGD:5509061 20190502 MGI 1316526 Zbtb5 zinc finger and BTB domain containing 5 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1316526 Zbtb5 zinc finger and BTB domain containing 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1316526 Zbtb5 zinc finger and BTB domain containing 5 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1316526 Zbtb5 zinc finger and BTB domain containing 5 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20201022 MGI 1316526 Zbtb5 zinc finger and BTB domain containing 5 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20201022 MGI 1316526 Zbtb5 zinc finger and BTB domain containing 5 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1316526 Zbtb5 zinc finger and BTB domain containing 5 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1316526 Zbtb5 zinc finger and BTB domain containing 5 gene MP:0005287 narrow eye opening IEA N RGD:5509061 20201022 MGI 1316526 Zbtb5 zinc finger and BTB domain containing 5 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1316526 Zbtb5 zinc finger and BTB domain containing 5 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1316529 Smyd4 SET and MYND domain containing 4 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20160915 MGI PMID:24652767 1316529 Smyd4 SET and MYND domain containing 4 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1316529 Smyd4 SET and MYND domain containing 4 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20160915 MGI PMID:24652767 1316531 Cdh5 cadherin 5 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21857650 1316531 Cdh5 cadherin 5 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21857650 1316531 Cdh5 cadherin 5 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:10428027 1316531 Cdh5 cadherin 5 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10428027 1316531 Cdh5 cadherin 5 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20151001 MGI PMID:24567373 1316531 Cdh5 cadherin 5 gene MP:0000601 small liver IAGP N RGD:5509061 20151001 MGI PMID:24567373 1316531 Cdh5 cadherin 5 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20160623 MGI PMID:24858856 1316531 Cdh5 cadherin 5 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20160623 MGI PMID:24858856 1316531 Cdh5 cadherin 5 gene MP:0001619 abnormal vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:21857650 1316531 Cdh5 cadherin 5 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:10428027 1316531 Cdh5 cadherin 5 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:15855637 1316531 Cdh5 cadherin 5 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:10428027 1316531 Cdh5 cadherin 5 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10428027 1316531 Cdh5 cadherin 5 gene MP:0001785 edema IAGP N RGD:5509061 20160623 MGI PMID:24858856 1316531 Cdh5 cadherin 5 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20151001 MGI PMID:24567373 1316531 Cdh5 cadherin 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20230511 MGI PMID:33497368 1316531 Cdh5 cadherin 5 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20160623 MGI PMID:24858856 1316531 Cdh5 cadherin 5 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20151001 MGI PMID:24567373 1316531 Cdh5 cadherin 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21857650 1316531 Cdh5 cadherin 5 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22975327 1316531 Cdh5 cadherin 5 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20160623 MGI PMID:24858856 1316531 Cdh5 cadherin 5 gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:22025303 1316531 Cdh5 cadherin 5 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:21857650 1316531 Cdh5 cadherin 5 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10428027 1316531 Cdh5 cadherin 5 gene MP:0003230 abnormal umbilical artery morphology IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:10428027 1316531 Cdh5 cadherin 5 gene MP:0003390 lymphedema IAGP N RGD:5509061 20151001 MGI PMID:24567373 1316531 Cdh5 cadherin 5 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20151001 MGI PMID:24567373 1316531 Cdh5 cadherin 5 gene MP:0003411 abnormal vein development IAGP N RGD:5509061 20141003 MGI PMID:10428027 1316531 Cdh5 cadherin 5 gene MP:0003542 abnormal vascular endothelial cell development IAGP N RGD:5509061 20141003 MGI PMID:10428027 1316531 Cdh5 cadherin 5 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0004832 enlarged ovary IAGP N RGD:5509061 20160623 MGI PMID:24858856 1316531 Cdh5 cadherin 5 gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20160623 MGI PMID:24858856 1316531 Cdh5 cadherin 5 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:21857650 1316531 Cdh5 cadherin 5 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20230511 MGI PMID:33497368 1316531 Cdh5 cadherin 5 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20230511 MGI PMID:33497368 1316531 Cdh5 cadherin 5 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10428027 1316531 Cdh5 cadherin 5 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20160623 MGI PMID:24858856 1316531 Cdh5 cadherin 5 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:10428027 1316531 Cdh5 cadherin 5 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:10428027 1316531 Cdh5 cadherin 5 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20151001 MGI PMID:24567373 1316531 Cdh5 cadherin 5 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:22025303 1316531 Cdh5 cadherin 5 gene MP:0009083 uterus hypertrophy IAGP N RGD:5509061 20160623 MGI PMID:24858856 1316531 Cdh5 cadherin 5 gene MP:0009251 enlarged endometrial glands IAGP N RGD:5509061 20160623 MGI PMID:24858856 1316531 Cdh5 cadherin 5 gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20160623 MGI PMID:24858856 1316531 Cdh5 cadherin 5 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20230511 MGI PMID:33497368 1316531 Cdh5 cadherin 5 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:21857650 1316531 Cdh5 cadherin 5 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:22025303 1316531 Cdh5 cadherin 5 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20151217 MGI PMID:24487320 1316531 Cdh5 cadherin 5 gene MP:0010195 abnormal lymphatic vessel endothelium morphology IAGP N RGD:5509061 20151001 MGI PMID:24567373 1316531 Cdh5 cadherin 5 gene MP:0010197 abnormal lymphatic vessel endothelial cell morphology IAGP N RGD:5509061 20151001 MGI PMID:24567373 1316531 Cdh5 cadherin 5 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20151001 MGI PMID:24567373 1316531 Cdh5 cadherin 5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21857650 1316531 Cdh5 cadherin 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10428027 1316531 Cdh5 cadherin 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20151001 MGI PMID:24567373 1316531 Cdh5 cadherin 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20151001 MGI PMID:24567373 1316531 Cdh5 cadherin 5 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20151001 MGI PMID:24567373 1316531 Cdh5 cadherin 5 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21857650 1316531 Cdh5 cadherin 5 gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:10428027 1316531 Cdh5 cadherin 5 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10428027 1316531 Cdh5 cadherin 5 gene MP:0012300 abnormal umbilical cord blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10207135 1316531 Cdh5 cadherin 5 gene MP:0013398 uterus fibrosis IAGP N RGD:5509061 20160623 MGI PMID:24858856 1316531 Cdh5 cadherin 5 gene MP:0013607 ovary fibrosis IAGP N RGD:5509061 20160623 MGI PMID:24858856 1316531 Cdh5 cadherin 5 gene MP:0014400 increased hematopoietic precursor cell number IAGP N RGD:5509061 20240321 MGI PMID:24567373 1316537 Dnajb11 DnaJ heat shock protein family (Hsp40) member B11 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1316537 Dnajb11 DnaJ heat shock protein family (Hsp40) member B11 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1316537 Dnajb11 DnaJ heat shock protein family (Hsp40) member B11 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20201022 MGI 1316537 Dnajb11 DnaJ heat shock protein family (Hsp40) member B11 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1316537 Dnajb11 DnaJ heat shock protein family (Hsp40) member B11 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1316537 Dnajb11 DnaJ heat shock protein family (Hsp40) member B11 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1316537 Dnajb11 DnaJ heat shock protein family (Hsp40) member B11 gene MP:0010574 dilated aorta IEA N RGD:5509061 20211021 MGI 1316537 Dnajb11 DnaJ heat shock protein family (Hsp40) member B11 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1316540 Tarbp2 TARBP2, RISC loading complex RNA binding subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10369260 1316540 Tarbp2 TARBP2, RISC loading complex RNA binding subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150813 MGI PMID:26029872 1316540 Tarbp2 TARBP2, RISC loading complex RNA binding subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20150813 MGI PMID:26029872 1316540 Tarbp2 TARBP2, RISC loading complex RNA binding subunit gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10369260 1316540 Tarbp2 TARBP2, RISC loading complex RNA binding subunit gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10369260 1316540 Tarbp2 TARBP2, RISC loading complex RNA binding subunit gene MP:0002083 premature death IAGP N RGD:5509061 20150813 MGI PMID:26029872 1316540 Tarbp2 TARBP2, RISC loading complex RNA binding subunit gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10369260 1316540 Tarbp2 TARBP2, RISC loading complex RNA binding subunit gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20150813 MGI PMID:26029872 1316540 Tarbp2 TARBP2, RISC loading complex RNA binding subunit gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20150813 MGI PMID:26029872 1316540 Tarbp2 TARBP2, RISC loading complex RNA binding subunit gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20150813 MGI PMID:26029872 1316540 Tarbp2 TARBP2, RISC loading complex RNA binding subunit gene MP:0004937 dilated heart IAGP N RGD:5509061 20150813 MGI PMID:26029872 1316540 Tarbp2 TARBP2, RISC loading complex RNA binding subunit gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20150813 MGI PMID:26029872 1316540 Tarbp2 TARBP2, RISC loading complex RNA binding subunit gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10369260 1316540 Tarbp2 TARBP2, RISC loading complex RNA binding subunit gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20150813 MGI PMID:26029872 1316540 Tarbp2 TARBP2, RISC loading complex RNA binding subunit gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:26029872 1316542 Rpa1 replication protein A1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1316542 Rpa1 replication protein A1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15965476 1316542 Rpa1 replication protein A1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15965476 1316542 Rpa1 replication protein A1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15965476 1316542 Rpa1 replication protein A1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1316542 Rpa1 replication protein A1 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20211021 MGI 1316542 Rpa1 replication protein A1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 1316542 Rpa1 replication protein A1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1316542 Rpa1 replication protein A1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1316542 Rpa1 replication protein A1 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:15965476 1316542 Rpa1 replication protein A1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15965476 1316542 Rpa1 replication protein A1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20181227 MGI 1316542 Rpa1 replication protein A1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15965476 1316542 Rpa1 replication protein A1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316542 Rpa1 replication protein A1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15965476 1316542 Rpa1 replication protein A1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1316542 Rpa1 replication protein A1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1316543 Klc2 kinesin light chain 2 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20211021 MGI 1316543 Klc2 kinesin light chain 2 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20240321 MGI PMID:34014435 1316543 Klc2 kinesin light chain 2 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20240321 MGI PMID:34014435 1316543 Klc2 kinesin light chain 2 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20240321 MGI PMID:34014435 1316543 Klc2 kinesin light chain 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20240321 MGI PMID:34014435 1316543 Klc2 kinesin light chain 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1316543 Klc2 kinesin light chain 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20240321 MGI PMID:34014435 1316543 Klc2 kinesin light chain 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20240321 MGI PMID:34014435 1316543 Klc2 kinesin light chain 2 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20170105 MGI 1316544 Scart1 scavenger receptor family member expressed on T cells 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0003109 short femur IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230601 MGI 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20240523 MGI 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20240523 MGI 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0014107 premature chondrocyte differentiation IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316545 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20190919 MGI PMID:31246957 1316548 Jmjd8 jumonji domain containing 8 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20221201 MGI PMID:34957483 1316548 Jmjd8 jumonji domain containing 8 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20221201 MGI PMID:34957483 1316548 Jmjd8 jumonji domain containing 8 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20221201 MGI PMID:34957483 1316548 Jmjd8 jumonji domain containing 8 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20180315 MGI PMID:27199445 1316548 Jmjd8 jumonji domain containing 8 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220811 MGI 1316548 Jmjd8 jumonji domain containing 8 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20221201 MGI PMID:34957483 1316548 Jmjd8 jumonji domain containing 8 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20221201 MGI PMID:34957483 1316548 Jmjd8 jumonji domain containing 8 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20221201 MGI PMID:34957483 1316548 Jmjd8 jumonji domain containing 8 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20180315 MGI PMID:27199445 1316548 Jmjd8 jumonji domain containing 8 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20221201 MGI PMID:34957483 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:12697906 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:12697906 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12697906 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:12697906 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:12697906 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:12697906 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001220 epidermal necrosis IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:16354193 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20180531 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12697906 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001435 absent suckling reflex IAGP N RGD:5509061 20141003 MGI PMID:12697906 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:12697906 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:16354193 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:16354193 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0009602 abnormal keratohyalin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0009607 decreased keratohyalin granule size IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20170921 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12697906 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23226340 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14512415 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0011159 abnormal epidermal-dermal junction morphology IAGP N RGD:5509061 20180531 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0030572 abnormal pilosebaceous unit morphology IAGP N RGD:5509061 20180607 MGI PMID:12821645 1316552 Slc27a4 solute carrier family 27 (fatty acid transporter), member 4 gene MP:0030798 joint contracture IAGP N RGD:5509061 20181011 MGI PMID:12821645 1316554 Il21 interleukin 21 gene MP:0001148 enlarged testis IEA N RGD:5509061 20231207 MGI 1316554 Il21 interleukin 21 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17581589 1316554 Il21 interleukin 21 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22466669 1316554 Il21 interleukin 21 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:18602282 1316554 Il21 interleukin 21 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18602282 1316554 Il21 interleukin 21 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16979605 1316554 Il21 interleukin 21 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:18546146 1316554 Il21 interleukin 21 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:17581589 1316554 Il21 interleukin 21 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:16979605 1316554 Il21 interleukin 21 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18602282 1316554 Il21 interleukin 21 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17581589 1316554 Il21 interleukin 21 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:18602282 1316554 Il21 interleukin 21 gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18602282 1316554 Il21 interleukin 21 gene MP:0008343 abnormal gamma-delta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17581589 1316554 Il21 interleukin 21 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:18602282 1316554 Il21 interleukin 21 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18602282 1316554 Il21 interleukin 21 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:17581589 1316556 Hcfc2 host cell factor C2 gene MP:0002419 abnormal innate immunity IEA N RGD:5509061 20180125 MGI 1316556 Hcfc2 host cell factor C2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20180125 MGI PMID:28970238 1316556 Hcfc2 host cell factor C2 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20180125 MGI PMID:28970238 1316556 Hcfc2 host cell factor C2 gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20180125 MGI PMID:28970238 1316556 Hcfc2 host cell factor C2 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20180125 MGI PMID:28970238 1316556 Hcfc2 host cell factor C2 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:28970238 1316556 Hcfc2 host cell factor C2 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:28970238 1316556 Hcfc2 host cell factor C2 gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:28970238 1316558 Gem GTP binding protein overexpressed in skeletal muscle gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:22761801 1316558 Gem GTP binding protein overexpressed in skeletal muscle gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22761801 1316558 Gem GTP binding protein overexpressed in skeletal muscle gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:22761801 1316558 Gem GTP binding protein overexpressed in skeletal muscle gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22761801 1316560 Nlrp10 NLR family, pyrin domain containing 10 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22538615 1316560 Nlrp10 NLR family, pyrin domain containing 10 gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:22538615 1316560 Nlrp10 NLR family, pyrin domain containing 10 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:22538615 1316560 Nlrp10 NLR family, pyrin domain containing 10 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:22538615 1316560 Nlrp10 NLR family, pyrin domain containing 10 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22538615 1316560 Nlrp10 NLR family, pyrin domain containing 10 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22538615 1316560 Nlrp10 NLR family, pyrin domain containing 10 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22538615 1316560 Nlrp10 NLR family, pyrin domain containing 10 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:22538615 1316560 Nlrp10 NLR family, pyrin domain containing 10 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:22538615 1316561 Rtl1 retrotransposon Gaglike 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:18176565 1316561 Rtl1 retrotransposon Gaglike 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:18176565 1316561 Rtl1 retrotransposon Gaglike 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18176565 1316561 Rtl1 retrotransposon Gaglike 1 gene MP:0004258 abnormal placenta size IAGP N RGD:5509061 20141003 MGI PMID:18176565 1316561 Rtl1 retrotransposon Gaglike 1 gene MP:0004260 enlarged placenta IAGP N RGD:5509061 20141003 MGI PMID:18176565 1316561 Rtl1 retrotransposon Gaglike 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:18176565 1316561 Rtl1 retrotransposon Gaglike 1 gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:18176565 1316561 Rtl1 retrotransposon Gaglike 1 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:18176565 1316561 Rtl1 retrotransposon Gaglike 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18176565 1316561 Rtl1 retrotransposon Gaglike 1 gene MP:0006372 impaired placental function IAGP N RGD:5509061 20141003 MGI PMID:18176565 1316561 Rtl1 retrotransposon Gaglike 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18176565 1316561 Rtl1 retrotransposon Gaglike 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18176565 1316561 Rtl1 retrotransposon Gaglike 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18176565 1316561 Rtl1 retrotransposon Gaglike 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18176565 1316563 Mbd3 methyl-CpG binding domain protein 3 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21196933 1316563 Mbd3 methyl-CpG binding domain protein 3 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:21196933 1316563 Mbd3 methyl-CpG binding domain protein 3 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:21196933 1316563 Mbd3 methyl-CpG binding domain protein 3 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21196933 1316563 Mbd3 methyl-CpG binding domain protein 3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11274056 1316563 Mbd3 methyl-CpG binding domain protein 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11274056 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:3986619 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0000745 tremors IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0001394 circling IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:423972 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:23055939 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0001575 cyanosis IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20191212 MGI PMID:30995482 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:23055939 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:423972 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0002623 abnormal vestibular hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:3986619 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:423972 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:423972 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20191212 MGI PMID:30995482 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004249 abnormal crista ampullaris morphology IEA N RGD:5509061 20141003 MGI 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004312 absent pillar cells IAGP N RGD:5509061 20141003 MGI PMID:423972 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004328 decreased vestibular hair cell number IAGP N RGD:5509061 20141003 MGI PMID:23055939 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:3986619 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004334 utricular macular degeneration IAGP N RGD:5509061 20141003 MGI PMID:3986619 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:423972 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8820880 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:23055939 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004397 absent cochlear inner hair cells IAGP N RGD:5509061 20141003 MGI PMID:423972 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:8820880 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004518 absent vestibular hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:23055939 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004589 abnormal cochlear hair cell development IEA N RGD:5509061 20210805 MGI 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:16730938 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20191212 MGI PMID:30995482 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0005191 head tilt IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0005307 head tossing IEA N RGD:5509061 20210805 MGI 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0006335 abnormal hearing electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:4067076 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0006336 abnormal otoacoustic response IAGP N RGD:5509061 20141003 MGI PMID:4067076 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20191212 MGI PMID:30995482 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16730938 1316565 Srrm4 serine/arginine repetitive matrix 4 gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20161208 MGI PMID:25838543 1316568 Wdr89 WD repeat domain 89 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210520 MGI 1316575 Mrps21 mitochondrial ribosomal protein S21 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316579 Eepd1 endonuclease/exonuclease/phosphatase family domain containing 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1316580 Slc23a3 solute carrier family 23 (nucleobase transporters), member 3 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20181227 MGI 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18536716 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000692 small spleen IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000706 small thymus IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:12589020 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12589020 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:12589020 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001127 small ovary IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001147 small testis IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12589020 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12589020 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12589020 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12589020 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:23955081 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190808 MGI 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12589020 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001925 male infertility IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001926 female infertility IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23410975 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12589020 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18536716 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12589020 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17395774 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160204 MGI PMID:23955081 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:12589020 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18536716 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23955081 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0002861 abnormal tail bud morphology IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0003582 abnormal ovary development IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004342 scapular bone foramen IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004446 split exoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004710 small notochord IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004713 split notochord IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:23955081 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23955081 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0006305 abnormal optic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0006338 abnormal second pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20808772 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18536716 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:12589020 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0009015 short proestrus IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0009018 short estrus IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0009020 prolonged metestrus IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0009231 detached acrosome IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0009233 enlarged sperm head IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7926765 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20141003 MGI PMID:18366140 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0012180 abnormal somatic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0012264 hindbrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23955081 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23955081 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0012435 decreased colon tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23955081 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0012659 decreased superoxide dismutase level IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0013482 abnormal duodenum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20150319 MGI PMID:18536716 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0013483 abnormal jejunum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20150319 MGI PMID:18536716 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0013662 decreased myeloid cell number IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0013693 abnormal hemopoiesis IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0013892 increased common lymphocyte progenitor cell number IAGP N RGD:5509061 20151112 MGI PMID:22185780 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0014269 decreased testes secretion IAGP N RGD:5509061 20230810 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20220120 MGI PMID:29559852 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0030834 acromion hypoplasia IAGP N RGD:5509061 20181018 MGI PMID:11290297 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0031018 decreased granulosa cell proliferation IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220120 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:30906217 1316582 Bmi1 Bmi1 polycomb ring finger oncogene gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:30906217 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11018075 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11018075 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0002658 abnormal liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0002698 abnormal sclera morphology IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:11018075 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0003328 portal hypertension IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0003415 priapism IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20201001 MGI PMID:11018075 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:11018075 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0005098 abnormal optic choroid morphology IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0005187 abnormal penis morphology IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20150416 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0006137 venoocclusion IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11018075 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0020407 abnormal placental thrombosis IAGP N RGD:5509061 20161124 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20200917 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:14592998 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:11895779 1316584 Serpinc1 serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1 gene MP:0031432 cornea perforation IAGP N RGD:5509061 20220721 MGI PMID:14592998 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17130243 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17130243 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20230601 MGI 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17130243 1316587 Cxcl14 C-X-C motif chemokine ligand 14 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:17724031 1316589 Dazap2 DAZ associated protein 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1316589 Dazap2 DAZ associated protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10373015 1316589 Dazap2 DAZ associated protein 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20230119 MGI 1316589 Dazap2 DAZ associated protein 2 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20230119 MGI 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22615130 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22615130 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22851594 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20181227 MGI 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151210 MGI PMID:22851594 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22615127 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:22615130 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:22615130 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0005461 abnormal dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22851594 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:22615130 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22615130 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22851594 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22851594 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22615130 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22851594 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20141003 MGI PMID:22851594 1316590 Zbtb46 zinc finger and BTB domain containing 46 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1316592 Tepsin TEPSIN, adaptor related protein complex 4 accessory protein gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1316595 Ido2 indoleamine 2,3-dioxygenase 2 gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20240215 MGI PMID:34965962 1316595 Ido2 indoleamine 2,3-dioxygenase 2 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141030 MGI PMID:24402311 1316595 Ido2 indoleamine 2,3-dioxygenase 2 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141030 MGI PMID:24402311 1316595 Ido2 indoleamine 2,3-dioxygenase 2 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20240215 MGI PMID:34965962 1316595 Ido2 indoleamine 2,3-dioxygenase 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141030 MGI PMID:24402311 1316595 Ido2 indoleamine 2,3-dioxygenase 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141030 MGI PMID:24402311 1316595 Ido2 indoleamine 2,3-dioxygenase 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141030 MGI PMID:24402311 1316595 Ido2 indoleamine 2,3-dioxygenase 2 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141030 MGI PMID:24402311 1316599 Dusp14 dual specificity phosphatase 14 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20180920 MGI PMID:26891723 1316599 Dusp14 dual specificity phosphatase 14 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20190418 MGI PMID:24403530 1316599 Dusp14 dual specificity phosphatase 14 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20190418 MGI PMID:24403530 1316599 Dusp14 dual specificity phosphatase 14 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20180920 MGI PMID:26891723 1316599 Dusp14 dual specificity phosphatase 14 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20190418 MGI PMID:24403530 1316599 Dusp14 dual specificity phosphatase 14 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20180920 MGI PMID:26891723 1316599 Dusp14 dual specificity phosphatase 14 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20180920 MGI PMID:26891723 1316599 Dusp14 dual specificity phosphatase 14 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20180920 MGI PMID:26891723 1316599 Dusp14 dual specificity phosphatase 14 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20190418 MGI PMID:24403530 1316599 Dusp14 dual specificity phosphatase 14 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20180920 MGI PMID:26891723 1316599 Dusp14 dual specificity phosphatase 14 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20190418 MGI PMID:24403530 1316599 Dusp14 dual specificity phosphatase 14 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20180920 MGI PMID:26891723 1316599 Dusp14 dual specificity phosphatase 14 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20190418 MGI PMID:24403530 1316599 Dusp14 dual specificity phosphatase 14 gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20190418 MGI PMID:24403530 1316599 Dusp14 dual specificity phosphatase 14 gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20180920 MGI PMID:26891723 1316608 Plxnc1 plexin C1 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20231207 MGI 1316608 Plxnc1 plexin C1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1316608 Plxnc1 plexin C1 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1316608 Plxnc1 plexin C1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1316608 Plxnc1 plexin C1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1316608 Plxnc1 plexin C1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1316608 Plxnc1 plexin C1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12879062 1316608 Plxnc1 plexin C1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1316608 Plxnc1 plexin C1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17356169 1316608 Plxnc1 plexin C1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1316608 Plxnc1 plexin C1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1316608 Plxnc1 plexin C1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1316608 Plxnc1 plexin C1 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 1316608 Plxnc1 plexin C1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17356169 1316610 Foxi1 forkhead box I1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:9843211 1316610 Foxi1 forkhead box I1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0000525 renal tubular acidosis IAGP N RGD:5509061 20141003 MGI PMID:15173882 1316610 Foxi1 forkhead box I1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:9843211 1316610 Foxi1 forkhead box I1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:9843211 1316610 Foxi1 forkhead box I1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:9843211 1316610 Foxi1 forkhead box I1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16932748 1316610 Foxi1 forkhead box I1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:16932748 1316610 Foxi1 forkhead box I1 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0003147 absent cochlea IAGP N RGD:5509061 20141003 MGI PMID:9843211 1316610 Foxi1 forkhead box I1 gene MP:0003226 absent cochlear modiolus IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0004314 absent inner ear vestibule IAGP N RGD:5509061 20141003 MGI PMID:9843211 1316610 Foxi1 forkhead box I1 gene MP:0004316 enlarged vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0004335 enlarged utricle IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0004410 absent endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:16932748 1316610 Foxi1 forkhead box I1 gene MP:0004922 abnormal common crus morphology IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0004928 increased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:16932748 1316610 Foxi1 forkhead box I1 gene MP:0004931 enlarged epididymis IAGP N RGD:5509061 20141003 MGI PMID:16932748 1316610 Foxi1 forkhead box I1 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:9843211 1316610 Foxi1 forkhead box I1 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0006014 dilated endolymphatic sac IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0006015 dilated lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0006016 dilated posterior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0006287 inner ear cyst IAGP N RGD:5509061 20141003 MGI PMID:12642503 1316610 Foxi1 forkhead box I1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:9843211 1316610 Foxi1 forkhead box I1 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:9843211 1316610 Foxi1 forkhead box I1 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:16932748 1316610 Foxi1 forkhead box I1 gene MP:0009349 increased urine pH IAGP N RGD:5509061 20141003 MGI PMID:15173882 1316610 Foxi1 forkhead box I1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9843211 1316610 Foxi1 forkhead box I1 gene MP:0011843 abnormal kidney collecting duct epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15173882 1316610 Foxi1 forkhead box I1 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220303 MGI PMID:16932748 1316611 Fcamr Fc receptor, IgA, IgM, high affinity gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:19549827 1316611 Fcamr Fc receptor, IgA, IgM, high affinity gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:19549827 1316611 Fcamr Fc receptor, IgA, IgM, high affinity gene MP:0008095 abnormal memory B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19549827 1316611 Fcamr Fc receptor, IgA, IgM, high affinity gene MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19549827 1316611 Fcamr Fc receptor, IgA, IgM, high affinity gene MP:0008198 abnormal follicular dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:19549827 1316611 Fcamr Fc receptor, IgA, IgM, high affinity gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:19549827 1316611 Fcamr Fc receptor, IgA, IgM, high affinity gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:19549827 1316612 Tmem97 transmembrane protein 97 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20231207 MGI 1316612 Tmem97 transmembrane protein 97 gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 1316612 Tmem97 transmembrane protein 97 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20230601 MGI 1316612 Tmem97 transmembrane protein 97 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20231207 MGI 1316612 Tmem97 transmembrane protein 97 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20231207 MGI 1316612 Tmem97 transmembrane protein 97 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201022 MGI PMID:32588039 1316612 Tmem97 transmembrane protein 97 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1316614 Irx3 Iroquois related homeobox 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:22992950 1316614 Irx3 Iroquois related homeobox 3 gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20141003 MGI PMID:22992950 1316614 Irx3 Iroquois related homeobox 3 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:22992950 1316614 Irx3 Iroquois related homeobox 3 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20200402 MGI 1316614 Irx3 Iroquois related homeobox 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150305 MGI PMID:24646999 1316614 Irx3 Iroquois related homeobox 3 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20181227 MGI 1316614 Irx3 Iroquois related homeobox 3 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:22992950 1316614 Irx3 Iroquois related homeobox 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20150305 MGI PMID:24646999 1316614 Irx3 Iroquois related homeobox 3 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:21825130 1316614 Irx3 Iroquois related homeobox 3 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:22992950 1316614 Irx3 Iroquois related homeobox 3 gene MP:0003898 abnormal QRS complex IAGP N RGD:5509061 20141003 MGI PMID:21825130 1316614 Irx3 Iroquois related homeobox 3 gene MP:0004116 abnormal atrioventricular bundle conduction IAGP N RGD:5509061 20141003 MGI PMID:21825130 1316614 Irx3 Iroquois related homeobox 3 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20150305 MGI PMID:24646999 1316614 Irx3 Iroquois related homeobox 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20150305 MGI PMID:24646999 1316614 Irx3 Iroquois related homeobox 3 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20150305 MGI PMID:24646999 1316614 Irx3 Iroquois related homeobox 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20150305 MGI PMID:24646999 1316614 Irx3 Iroquois related homeobox 3 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20150305 MGI PMID:24646999 1316614 Irx3 Iroquois related homeobox 3 gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141003 MGI PMID:22992950 1316614 Irx3 Iroquois related homeobox 3 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:22992950 1316614 Irx3 Iroquois related homeobox 3 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20150305 MGI PMID:24646999 1316614 Irx3 Iroquois related homeobox 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1316614 Irx3 Iroquois related homeobox 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1316614 Irx3 Iroquois related homeobox 3 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:21825130 1316614 Irx3 Iroquois related homeobox 3 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:22992950 1316614 Irx3 Iroquois related homeobox 3 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:22992950 1316614 Irx3 Iroquois related homeobox 3 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:22992950 1316614 Irx3 Iroquois related homeobox 3 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:21825130 1316614 Irx3 Iroquois related homeobox 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22992950 1316614 Irx3 Iroquois related homeobox 3 gene MP:0011919 abnormal R wave IAGP N RGD:5509061 20141003 MGI PMID:21825130 1316614 Irx3 Iroquois related homeobox 3 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1316614 Irx3 Iroquois related homeobox 3 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:24646999 1316616 Srsf7 serine and arginine-rich splicing factor 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20211028 MGI PMID:32146325 1316616 Srsf7 serine and arginine-rich splicing factor 7 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20211028 MGI PMID:32146325 1316616 Srsf7 serine and arginine-rich splicing factor 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316616 Srsf7 serine and arginine-rich splicing factor 7 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:32146325 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0000414 alopecia IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0000705 athymia IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0001836 abnormal antigen presentation via MHC class I IAGP N RGD:5509061 20141003 MGI PMID:22197977 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:22197977 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0002083 premature death IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16709825 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0002453 abnormal B lymphocyte antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:22197977 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:22197977 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0005046 absent spleen white pulp IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16709825 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16709825 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16709825 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22197977 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0008591 increased circulating interleukin-1 level IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316620 Psmb10 proteasome (prosome, macropain) subunit, beta type 10 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20180524 MGI PMID:29654304 1316630 Tbc1d2b TBC1 domain family, member 2B gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1316630 Tbc1d2b TBC1 domain family, member 2B gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160804 MGI 1316630 Tbc1d2b TBC1 domain family, member 2B gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20141003 MGI 1316635 Siglecg sialic acid binding Ig-like lectin G gene MP:0001806 decreased IgM level IEA N RGD:5509061 20181011 MGI 1316635 Siglecg sialic acid binding Ig-like lectin G gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:17572677 1316635 Siglecg sialic acid binding Ig-like lectin G gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:17572677 1316635 Siglecg sialic acid binding Ig-like lectin G gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:17912374 1316635 Siglecg sialic acid binding Ig-like lectin G gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:17912374 1316635 Siglecg sialic acid binding Ig-like lectin G gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:17572677 1316635 Siglecg sialic acid binding Ig-like lectin G gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17572677 1316635 Siglecg sialic acid binding Ig-like lectin G gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:17572677 1316635 Siglecg sialic acid binding Ig-like lectin G gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:17912374 1316635 Siglecg sialic acid binding Ig-like lectin G gene MP:0008169 increased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:17572677 1316635 Siglecg sialic acid binding Ig-like lectin G gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20181011 MGI 1316635 Siglecg sialic acid binding Ig-like lectin G gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:17572677 1316635 Siglecg sialic acid binding Ig-like lectin G gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20181011 MGI 1316635 Siglecg sialic acid binding Ig-like lectin G gene MP:0010839 decreased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20181011 MGI 1316637 Arid4a AT-rich interaction domain 4A gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0002445 abnormal mononuclear cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 1316637 Arid4a AT-rich interaction domain 4A gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 1316637 Arid4a AT-rich interaction domain 4A gene MP:0003121 genetic imprinting IAGP N RGD:5509061 20141003 MGI PMID:17043311 1316637 Arid4a AT-rich interaction domain 4A gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:17043311 1316637 Arid4a AT-rich interaction domain 4A gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:17043311 1316637 Arid4a AT-rich interaction domain 4A gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0004692 small pubis IAGP N RGD:5509061 20210930 MGI PMID:33905568 1316637 Arid4a AT-rich interaction domain 4A gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:17043311 1316637 Arid4a AT-rich interaction domain 4A gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:17043311 1316637 Arid4a AT-rich interaction domain 4A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17043311 1316637 Arid4a AT-rich interaction domain 4A gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1316637 Arid4a AT-rich interaction domain 4A gene MP:0011747 myelofibrosis IAGP N RGD:5509061 20141003 MGI PMID:18728284 1316637 Arid4a AT-rich interaction domain 4A gene MP:0031070 hemophagocytosis IAGP N RGD:5509061 20200618 MGI PMID:18728284 1316638 D130043K22Rik RIKEN cDNA D130043K22 gene gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20180208 MGI PMID:27510895 1316638 D130043K22Rik RIKEN cDNA D130043K22 gene gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1316638 D130043K22Rik RIKEN cDNA D130043K22 gene gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20180208 MGI PMID:27510895 1316639 Tmigd1 transmembrane and immunoglobulin domain containing 1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20210225 MGI PMID:33129760 1316639 Tmigd1 transmembrane and immunoglobulin domain containing 1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20210225 MGI PMID:33129760 1316641 Trim6 tripartite motif-containing 6 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20220811 MGI PMID:35533195 1316642 Nlrp5 NLR family, pyrin domain containing 5 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18804437 1316642 Nlrp5 NLR family, pyrin domain containing 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11062459 1316642 Nlrp5 NLR family, pyrin domain containing 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18804437 1316642 Nlrp5 NLR family, pyrin domain containing 5 gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20200423 MGI PMID:25208553 1316642 Nlrp5 NLR family, pyrin domain containing 5 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:11062459 1316642 Nlrp5 NLR family, pyrin domain containing 5 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:18804437 1316642 Nlrp5 NLR family, pyrin domain containing 5 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20200423 MGI PMID:25208553 1316642 Nlrp5 NLR family, pyrin domain containing 5 gene MP:0020850 abnormal microtubule cytoskeleton morphology IAGP N RGD:5509061 20200423 MGI PMID:25208553 1316647 Gin1 gypsy retrotransposon integrase 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1316647 Gin1 gypsy retrotransposon integrase 1 gene MP:0000277 abnormal heart shape IEA N RGD:5509061 20210128 MGI 1316647 Gin1 gypsy retrotransposon integrase 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1316647 Gin1 gypsy retrotransposon integrase 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1316653 Klhl1 kelch-like 1 gene MP:0000160 kyphosis IEA N RGD:5509061 20230601 MGI 1316653 Klhl1 kelch-like 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220811 MGI 1316653 Klhl1 kelch-like 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220811 MGI 1316653 Klhl1 kelch-like 1 gene MP:0000692 small spleen IEA N RGD:5509061 20220811 MGI 1316653 Klhl1 kelch-like 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220811 MGI 1316653 Klhl1 kelch-like 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220811 MGI 1316653 Klhl1 kelch-like 1 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:17005861 1316653 Klhl1 kelch-like 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220811 MGI 1316653 Klhl1 kelch-like 1 gene MP:0001147 small testis IEA N RGD:5509061 20220811 MGI 1316653 Klhl1 kelch-like 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20220519 MGI 1316653 Klhl1 kelch-like 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17005861 1316653 Klhl1 kelch-like 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17005861 1316653 Klhl1 kelch-like 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20221215 MGI 1316653 Klhl1 kelch-like 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220811 MGI 1316653 Klhl1 kelch-like 1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20220811 MGI 1316653 Klhl1 kelch-like 1 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20231207 MGI 1316653 Klhl1 kelch-like 1 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20220811 MGI 1316658 Tiam1 T cell lymphoma invasion and metastasis 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12075356 1316658 Tiam1 T cell lymphoma invasion and metastasis 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:22661025 1316658 Tiam1 T cell lymphoma invasion and metastasis 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:22661025 1316658 Tiam1 T cell lymphoma invasion and metastasis 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22661025 1316658 Tiam1 T cell lymphoma invasion and metastasis 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1316658 Tiam1 T cell lymphoma invasion and metastasis 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1316658 Tiam1 T cell lymphoma invasion and metastasis 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12075356 1316658 Tiam1 T cell lymphoma invasion and metastasis 1 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:22661025 1316658 Tiam1 T cell lymphoma invasion and metastasis 1 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12075356 1316658 Tiam1 T cell lymphoma invasion and metastasis 1 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12075356 1316658 Tiam1 T cell lymphoma invasion and metastasis 1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:12075356 1316658 Tiam1 T cell lymphoma invasion and metastasis 1 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20211021 MGI 1316664 Smpdl3b sphingomyelin phosphodiesterase, acid-like 3B gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20161124 MGI PMID:26095358 1316664 Smpdl3b sphingomyelin phosphodiesterase, acid-like 3B gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20141003 MGI 1316664 Smpdl3b sphingomyelin phosphodiesterase, acid-like 3B gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20161124 MGI PMID:26095358 1316664 Smpdl3b sphingomyelin phosphodiesterase, acid-like 3B gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20161124 MGI PMID:26095358 1316664 Smpdl3b sphingomyelin phosphodiesterase, acid-like 3B gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20161124 MGI PMID:26095358 1316664 Smpdl3b sphingomyelin phosphodiesterase, acid-like 3B gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20161124 MGI PMID:26095358 1316664 Smpdl3b sphingomyelin phosphodiesterase, acid-like 3B gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20161124 MGI PMID:26095358 1316664 Smpdl3b sphingomyelin phosphodiesterase, acid-like 3B gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20161124 MGI PMID:26095358 1316664 Smpdl3b sphingomyelin phosphodiesterase, acid-like 3B gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20161124 MGI PMID:26095358 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20220519 MGI 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20111116 MGI 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:8887273 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11944981 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:8476712 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:8887273 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:11944981 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0000644 dextrocardia IEA N RGD:5509061 20111116 MGI 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:11944981 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:1557392 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8887273 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:11944981 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:7723240 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:8341011 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:8476712 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:8887273 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20201022 MGI 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0001924 infertility IEA N RGD:5509061 20111116 MGI 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8476712 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11944981 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:19666828 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0002767 situs ambiguus IAGP N RGD:5509061 20141003 MGI PMID:19666828 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:8887273 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0002989 small kidney IEA N RGD:5509061 20201022 MGI 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:11944981 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:20215348 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:8341011 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:8476712 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:8887273 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20141003 MGI PMID:7723240 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003266 biliary cyst IAGP N RGD:5509061 20141003 MGI PMID:11944981 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003266 biliary cyst IAGP N RGD:5509061 20141003 MGI PMID:20215348 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:20215348 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:19666828 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:8476712 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:11944981 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:1557392 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:22258617 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:7723240 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:8341011 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:8476712 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:8887273 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0004133 heterotaxia IEA N RGD:5509061 20111116 MGI 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8476712 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:8341011 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:8476712 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:11944981 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:20215348 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0008933 abnormal motile primary cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:19666828 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:11944981 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0008992 abnormal portal lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:8887273 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0008993 abnormal portal triad morphology IAGP N RGD:5509061 20141003 MGI PMID:8887273 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:7723240 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0009342 enlarged gallbladder IAGP N RGD:5509061 20141003 MGI PMID:7723240 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0009343 dilated gallbladder IAGP N RGD:5509061 20141003 MGI PMID:8887273 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0009494 abnormal biliary ductule morphology IAGP N RGD:5509061 20141003 MGI PMID:11944981 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0009500 abnormal interlobular bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:11944981 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:11944981 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19666828 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1557392 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19666828 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7723240 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8887273 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11944981 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11944981 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20215348 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19666828 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20215348 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0011252 situs inversus totalis IEA N RGD:5509061 20111116 MGI 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20215348 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:8887273 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0011665 d-loop transposition of the great arteries IEA N RGD:5509061 20141003 MGI 1316666 Bicc1 BicC family RNA binding protein 1 gene MP:0012027 abnormal embryonic cilium location or orientation IAGP N RGD:5509061 20141003 MGI PMID:19666828 1316670 Cldn17 claudin 17 gene MP:0001426 polydipsia IAGP N RGD:5509061 20220714 MGI PMID:35681477 1316670 Cldn17 claudin 17 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220714 MGI PMID:35681477 1316670 Cldn17 claudin 17 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20220714 MGI PMID:35681477 1316670 Cldn17 claudin 17 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20220714 MGI PMID:35681477 1316670 Cldn17 claudin 17 gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20220714 MGI PMID:35681477 1316670 Cldn17 claudin 17 gene MP:0003016 increased circulating bicarbonate level IAGP N RGD:5509061 20220714 MGI PMID:35681477 1316670 Cldn17 claudin 17 gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20220714 MGI PMID:35681477 1316670 Cldn17 claudin 17 gene MP:0003267 constipation IAGP N RGD:5509061 20220714 MGI PMID:35681477 1316670 Cldn17 claudin 17 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220714 MGI PMID:35681477 1316670 Cldn17 claudin 17 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20220714 MGI PMID:35681477 1316670 Cldn17 claudin 17 gene MP:0005634 decreased circulating sodium level IAGP N RGD:5509061 20220714 MGI PMID:35681477 1316670 Cldn17 claudin 17 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20220714 MGI PMID:35681477 1316670 Cldn17 claudin 17 gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20220714 MGI PMID:35681477 1316670 Cldn17 claudin 17 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20220714 MGI PMID:35681477 1316670 Cldn17 claudin 17 gene MP:0012311 decreased defecation amount IAGP N RGD:5509061 20220714 MGI PMID:35681477 1316672 Krt14 keratin 14 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:17635993 1316672 Krt14 keratin 14 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17635993 1316672 Krt14 keratin 14 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:23792458 1316672 Krt14 keratin 14 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:17635993 1316672 Krt14 keratin 14 gene MP:0000404 decreased curvature of zigzag hairs IAGP N RGD:5509061 20141003 MGI PMID:17635993 1316672 Krt14 keratin 14 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:11371349 1316672 Krt14 keratin 14 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:19118220 1316672 Krt14 keratin 14 gene MP:0000414 alopecia IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:17635993 1316672 Krt14 keratin 14 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0000416 sparse hair IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1316672 Krt14 keratin 14 gene MP:0000467 abnormal esophagus morphology IAGP N RGD:5509061 20141003 MGI PMID:7539810 1316672 Krt14 keratin 14 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1316672 Krt14 keratin 14 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1316672 Krt14 keratin 14 gene MP:0000648 absent sebaceous gland IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0001140 abnormal vagina epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7539810 1316672 Krt14 keratin 14 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0001192 scaly skin IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0001193 psoriasis IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0001194 dermatitis IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:19118220 1316672 Krt14 keratin 14 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:11157990 1316672 Krt14 keratin 14 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:19118220 1316672 Krt14 keratin 14 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:7539810 1316672 Krt14 keratin 14 gene MP:0001212 skin lesions IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17118961 1316672 Krt14 keratin 14 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17635993 1316672 Krt14 keratin 14 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:23792458 1316672 Krt14 keratin 14 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0001224 abnormal keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17118961 1316672 Krt14 keratin 14 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:7539810 1316672 Krt14 keratin 14 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:17118961 1316672 Krt14 keratin 14 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:17635993 1316672 Krt14 keratin 14 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20181220 MGI PMID:22975380 1316672 Krt14 keratin 14 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20190124 MGI PMID:28096290 1316672 Krt14 keratin 14 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1316672 Krt14 keratin 14 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1316672 Krt14 keratin 14 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0001874 acanthosis IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1316672 Krt14 keratin 14 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:17118961 1316672 Krt14 keratin 14 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:11371349 1316672 Krt14 keratin 14 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:7539810 1316672 Krt14 keratin 14 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11157990 1316672 Krt14 keratin 14 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7539810 1316672 Krt14 keratin 14 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:19118220 1316672 Krt14 keratin 14 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20190124 MGI PMID:28096290 1316672 Krt14 keratin 14 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1316672 Krt14 keratin 14 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23792458 1316672 Krt14 keratin 14 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20181220 MGI PMID:22975380 1316672 Krt14 keratin 14 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20181220 MGI PMID:22975380 1316672 Krt14 keratin 14 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20190124 MGI PMID:28096290 1316672 Krt14 keratin 14 gene MP:0003853 dry skin IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0004126 thin hypodermis IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23736260 1316672 Krt14 keratin 14 gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20180913 MGI PMID:24162662 1316672 Krt14 keratin 14 gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17635993 1316672 Krt14 keratin 14 gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20190124 MGI PMID:28096290 1316672 Krt14 keratin 14 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20181220 MGI PMID:22975380 1316672 Krt14 keratin 14 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20190124 MGI PMID:28096290 1316672 Krt14 keratin 14 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23792458 1316672 Krt14 keratin 14 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20181220 MGI PMID:22975380 1316672 Krt14 keratin 14 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:19118220 1316672 Krt14 keratin 14 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:17635993 1316672 Krt14 keratin 14 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0008538 decreased zigzag hair amount IAGP N RGD:5509061 20141003 MGI PMID:17635993 1316672 Krt14 keratin 14 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:7539810 1316672 Krt14 keratin 14 gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20190124 MGI PMID:28096290 1316672 Krt14 keratin 14 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17635993 1316672 Krt14 keratin 14 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23792458 1316672 Krt14 keratin 14 gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20180913 MGI PMID:24162662 1316672 Krt14 keratin 14 gene MP:0009795 epidermal spongiosis IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20181220 MGI PMID:22975380 1316672 Krt14 keratin 14 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:17635993 1316672 Krt14 keratin 14 gene MP:0010202 focal dorsal hair loss IAGP N RGD:5509061 20141003 MGI PMID:17635993 1316672 Krt14 keratin 14 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20180913 MGI PMID:24162662 1316672 Krt14 keratin 14 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20181220 MGI PMID:22975380 1316672 Krt14 keratin 14 gene MP:0010318 increased salivary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23736260 1316672 Krt14 keratin 14 gene MP:0011015 decreased body surface temperature IAGP N RGD:5509061 20141003 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11157990 1316672 Krt14 keratin 14 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7539810 1316672 Krt14 keratin 14 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316672 Krt14 keratin 14 gene MP:0012022 increased melanocyte number IAGP N RGD:5509061 20190124 MGI PMID:28096290 1316672 Krt14 keratin 14 gene MP:0012110 increased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:23736260 1316672 Krt14 keratin 14 gene MP:0012193 increased keratinocyte migration IAGP N RGD:5509061 20141003 MGI PMID:23792458 1316672 Krt14 keratin 14 gene MP:0013374 increased sebaceous gland tumor incidence IAGP N RGD:5509061 20180913 MGI PMID:24162662 1316672 Krt14 keratin 14 gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:23918954 1316672 Krt14 keratin 14 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:23736260 1316672 Krt14 keratin 14 gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:7539810 1316672 Krt14 keratin 14 gene MP:0030529 abnormal head skin morphology IAGP N RGD:5509061 20180222 MGI PMID:29113991 1316672 Krt14 keratin 14 gene MP:0031395 cutaneous mastocytosis IAGP N RGD:5509061 20220721 MGI PMID:23918954 1316674 Banp BTG3 associated nuclear protein gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1316674 Banp BTG3 associated nuclear protein gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210826 MGI 1316674 Banp BTG3 associated nuclear protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316674 Banp BTG3 associated nuclear protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1316676 Mgme1 mitochondrial genome maintenance exonuclease 1 gene MP:0001577 anemia IAGP N RGD:5509061 20180503 MGI PMID:29572490 1316676 Mgme1 mitochondrial genome maintenance exonuclease 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1316676 Mgme1 mitochondrial genome maintenance exonuclease 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20180503 MGI PMID:29572490 1316676 Mgme1 mitochondrial genome maintenance exonuclease 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1316676 Mgme1 mitochondrial genome maintenance exonuclease 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20220519 MGI 1316676 Mgme1 mitochondrial genome maintenance exonuclease 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1316676 Mgme1 mitochondrial genome maintenance exonuclease 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180503 MGI PMID:29572490 1316676 Mgme1 mitochondrial genome maintenance exonuclease 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 1316676 Mgme1 mitochondrial genome maintenance exonuclease 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1316676 Mgme1 mitochondrial genome maintenance exonuclease 1 gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20180503 MGI PMID:29572490 1316676 Mgme1 mitochondrial genome maintenance exonuclease 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1316678 Cpne7 copine VII gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210128 MGI 1316678 Cpne7 copine VII gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1316678 Cpne7 copine VII gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20240530 MGI PMID:38105557 1316678 Cpne7 copine VII gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20240530 MGI PMID:38105557 1316678 Cpne7 copine VII gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201022 MGI 1316678 Cpne7 copine VII gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20240530 MGI PMID:38105557 1316678 Cpne7 copine VII gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1316678 Cpne7 copine VII gene MP:0013250 abnormal dental pulp morphology IAGP N RGD:5509061 20240530 MGI PMID:38105557 1316678 Cpne7 copine VII gene MP:0030453 abnormal odontoblast morphology IAGP N RGD:5509061 20240530 MGI PMID:38105557 1316678 Cpne7 copine VII gene MP:0030559 abnormal dental pulp canal morphology IAGP N RGD:5509061 20240530 MGI PMID:38105557 1316678 Cpne7 copine VII gene MP:0031626 increased dental pulp cell apoptosis IAGP N RGD:5509061 20240620 MGI PMID:38105557 1316680 Set SET nuclear oncogene gene MP:0000929 open neural tube IAGP N RGD:5509061 20190912 MGI PMID:30858352 1316680 Set SET nuclear oncogene gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20190912 MGI PMID:30858352 1316680 Set SET nuclear oncogene gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:30858352 1316680 Set SET nuclear oncogene gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:30858352 1316680 Set SET nuclear oncogene gene MP:0012270 cardiac edema IAGP N RGD:5509061 20190912 MGI PMID:30858352 1316681 Rell1 RELT-like 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1316681 Rell1 RELT-like 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1316681 Rell1 RELT-like 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1316681 Rell1 RELT-like 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220519 MGI 1316683 Zfp276 zinc finger protein (C2H2 type) 276 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20240425 MGI PMID:35137157 1316683 Zfp276 zinc finger protein (C2H2 type) 276 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20240425 MGI PMID:35137157 1316683 Zfp276 zinc finger protein (C2H2 type) 276 gene MP:0014318 abnormal oligodendrocyte differentiation IAGP N RGD:5509061 20240425 MGI PMID:35137157 1316683 Zfp276 zinc finger protein (C2H2 type) 276 gene MP:0020868 decreased lipogenesis IAGP N RGD:5509061 20240425 MGI PMID:35137157 1316686 Cyp39a1 cytochrome P450, family 39, subfamily a, polypeptide 1 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20240523 MGI 1316688 Pkp1 plakophilin 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0009598 thin epidermis stratum granulosum IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170601 MGI PMID:27033150 1316688 Pkp1 plakophilin 1 gene MP:0030605 abnormal corneocyte morphology IAGP N RGD:5509061 20180628 MGI PMID:27033150 1316689 Doc2g double C2, gamma gene MP:0002915 abnormal synaptic depression IAGP N RGD:5509061 20241031 MGI PMID:33753311 1316689 Doc2g double C2, gamma gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20241031 MGI PMID:33753311 1316689 Doc2g double C2, gamma gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20241031 MGI PMID:33753311 1316689 Doc2g double C2, gamma gene MP:0014253 decreased paired-pulse ratio IAGP N RGD:5509061 20241031 MGI PMID:33753311 1316700 Wdr3 WD repeat domain 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230406 MGI PMID:36463953 1316700 Wdr3 WD repeat domain 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20230406 MGI PMID:36463953 1316701 Ciao2a cytosolic iron-sulfur assembly component 2A gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20231207 MGI 1316703 Arid1b AT-rich interaction domain 1B gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 1316703 Arid1b AT-rich interaction domain 1B gene MP:0000747 muscle weakness IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001258 decreased body length IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001265 decreased body size IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20221215 MGI 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1316703 Arid1b AT-rich interaction domain 1B gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0002188 small heart IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0002989 small kidney IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20231207 MGI 1316703 Arid1b AT-rich interaction domain 1B gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0008831 abnormal insulin-like growth factor I level IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0009455 enhanced cued conditioning behavior IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0009456 impaired cued conditioning behavior IEA N RGD:5509061 20210128 MGI 1316703 Arid1b AT-rich interaction domain 1B gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1316703 Arid1b AT-rich interaction domain 1B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1316703 Arid1b AT-rich interaction domain 1B gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0012318 slow extinction of fear memory IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1316703 Arid1b AT-rich interaction domain 1B gene MP:0014115 cognitive inflexibility IAGP N RGD:5509061 20190418 MGI PMID:28867767 1316703 Arid1b AT-rich interaction domain 1B gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20201022 MGI 1316703 Arid1b AT-rich interaction domain 1B gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20210128 MGI 1316703 Arid1b AT-rich interaction domain 1B gene MP:0020594 decreased cerebral cortex cell number IAGP N RGD:5509061 20180621 MGI PMID:28695822 1316703 Arid1b AT-rich interaction domain 1B gene MP:0030981 abnormal dentate gyrus subgranular zone morphology IAGP N RGD:5509061 20191017 MGI PMID:28695822 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20141003 MGI 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20160804 MGI 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20170629 MGI PMID:25568313 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170629 MGI PMID:25568313 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20170629 MGI PMID:25568313 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20170629 MGI PMID:25568313 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20170518 MGI PMID:24646517 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:24646517 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20170629 MGI PMID:25568313 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20160804 MGI 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20170629 MGI PMID:27939640 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0008262 abnormal hippocampus region morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20170629 MGI PMID:25568313 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20170629 MGI PMID:25568313 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20170629 MGI PMID:25568313 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170629 MGI PMID:25568313 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20170518 MGI PMID:24646517 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170518 MGI PMID:24646517 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170629 MGI PMID:25568313 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20170518 MGI PMID:24646517 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20170629 MGI PMID:25568313 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20170518 MGI PMID:24646517 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0020069 decreased neocortex size IAGP N RGD:5509061 20170629 MGI PMID:25568313 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0020388 decreased radial glial cell number IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20170518 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20170629 MGI PMID:25568313 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0020536 increased subiculum size IAGP N RGD:5509061 20180301 MGI PMID:25757017 1316706 Brpf1 bromodomain and PHD finger containing, 1 gene MP:0030956 abnormal neuronal precursor cell migration IAGP N RGD:5509061 20190725 MGI PMID:25757017 1316708 Cpeb2 cytoplasmic polyadenylation element binding protein 2 gene MP:0001037 abnormal parasympathetic neuron morphology IAGP N RGD:5509061 20170420 MGI PMID:27810937 1316708 Cpeb2 cytoplasmic polyadenylation element binding protein 2 gene MP:0001945 bronchoconstriction IAGP N RGD:5509061 20170420 MGI PMID:27810937 1316708 Cpeb2 cytoplasmic polyadenylation element binding protein 2 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20170420 MGI PMID:27810937 1316708 Cpeb2 cytoplasmic polyadenylation element binding protein 2 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20170420 MGI PMID:27810937 1316708 Cpeb2 cytoplasmic polyadenylation element binding protein 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20170420 MGI PMID:27810937 1316708 Cpeb2 cytoplasmic polyadenylation element binding protein 2 gene MP:0001957 apnea IAGP N RGD:5509061 20170420 MGI PMID:27810937 1316708 Cpeb2 cytoplasmic polyadenylation element binding protein 2 gene MP:0002337 abnormal whole-body plethysmography IAGP N RGD:5509061 20170420 MGI PMID:27810937 1316708 Cpeb2 cytoplasmic polyadenylation element binding protein 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20170420 MGI PMID:27810937 1316708 Cpeb2 cytoplasmic polyadenylation element binding protein 2 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20170420 MGI PMID:27810937 1316708 Cpeb2 cytoplasmic polyadenylation element binding protein 2 gene MP:0006277 abnormal parasympathetic nervous system physiology IAGP N RGD:5509061 20170420 MGI PMID:27810937 1316708 Cpeb2 cytoplasmic polyadenylation element binding protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170420 MGI PMID:27810937 1316708 Cpeb2 cytoplasmic polyadenylation element binding protein 2 gene MP:0012593 increased brain choline acetyltransferase activity IAGP N RGD:5509061 20170420 MGI PMID:27810937 1316708 Cpeb2 cytoplasmic polyadenylation element binding protein 2 gene MP:0030676 increased acetylcholine level IAGP N RGD:5509061 20180927 MGI PMID:27810937 1316710 Hba-x hemoglobin X, alpha-like embryonic chain in Hba complex gene MP:0000226 abnormal mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:9242562 1316710 Hba-x hemoglobin X, alpha-like embryonic chain in Hba complex gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9242562 1316710 Hba-x hemoglobin X, alpha-like embryonic chain in Hba complex gene MP:0001588 abnormal hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:9242562 1316710 Hba-x hemoglobin X, alpha-like embryonic chain in Hba complex gene MP:0001589 abnormal mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:9242562 1316710 Hba-x hemoglobin X, alpha-like embryonic chain in Hba complex gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9242562 1316710 Hba-x hemoglobin X, alpha-like embryonic chain in Hba complex gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9242562 1316710 Hba-x hemoglobin X, alpha-like embryonic chain in Hba complex gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9242562 1316710 Hba-x hemoglobin X, alpha-like embryonic chain in Hba complex gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:9242562 1316710 Hba-x hemoglobin X, alpha-like embryonic chain in Hba complex gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:9242562 1316710 Hba-x hemoglobin X, alpha-like embryonic chain in Hba complex gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:9242562 1316710 Hba-x hemoglobin X, alpha-like embryonic chain in Hba complex gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:9242562 1316710 Hba-x hemoglobin X, alpha-like embryonic chain in Hba complex gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9242562 1316710 Hba-x hemoglobin X, alpha-like embryonic chain in Hba complex gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9242562 1316712 Cntrob centrobin, centrosomal BRCA2 interacting protein gene MP:0001925 male infertility IEA N RGD:5509061 20231207 MGI 1316713 AU040320 expressed sequence AU040320 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20181227 MGI 1316713 AU040320 expressed sequence AU040320 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20210520 MGI 1316713 AU040320 expressed sequence AU040320 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1316713 AU040320 expressed sequence AU040320 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1316713 AU040320 expressed sequence AU040320 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1316713 AU040320 expressed sequence AU040320 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1316713 AU040320 expressed sequence AU040320 gene MP:0001513 limb grasping IEA N RGD:5509061 20210128 MGI 1316713 AU040320 expressed sequence AU040320 gene MP:0001523 impaired righting response IEA N RGD:5509061 20210128 MGI 1316713 AU040320 expressed sequence AU040320 gene MP:0001925 male infertility IAGP N RGD:5509061 20220224 MGI PMID:29991750 1316713 AU040320 expressed sequence AU040320 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220224 MGI PMID:29991750 1316713 AU040320 expressed sequence AU040320 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210520 MGI 1316713 AU040320 expressed sequence AU040320 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220224 MGI PMID:29991750 1316713 AU040320 expressed sequence AU040320 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220224 MGI PMID:29991750 1316713 AU040320 expressed sequence AU040320 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220224 MGI PMID:29991750 1316713 AU040320 expressed sequence AU040320 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220519 MGI 1316713 AU040320 expressed sequence AU040320 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20220224 MGI PMID:29991750 1316713 AU040320 expressed sequence AU040320 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220224 MGI PMID:29991750 1316713 AU040320 expressed sequence AU040320 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220224 MGI PMID:29991750 1316713 AU040320 expressed sequence AU040320 gene MP:0009235 small sperm head IAGP N RGD:5509061 20220224 MGI PMID:29991750 1316713 AU040320 expressed sequence AU040320 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220224 MGI PMID:29991750 1316713 AU040320 expressed sequence AU040320 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220224 MGI PMID:29991750 1316713 AU040320 expressed sequence AU040320 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220224 MGI PMID:29991750 1316713 AU040320 expressed sequence AU040320 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220519 MGI 1316713 AU040320 expressed sequence AU040320 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1316713 AU040320 expressed sequence AU040320 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 1316713 AU040320 expressed sequence AU040320 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:29991750 1316713 AU040320 expressed sequence AU040320 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220224 MGI PMID:29991750 1316713 AU040320 expressed sequence AU040320 gene MP:0020923 decreased susceptibility to Parvoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:26814968 1316713 AU040320 expressed sequence AU040320 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220303 MGI PMID:29991750 1316713 AU040320 expressed sequence AU040320 gene MP:0031355 abnormal proacrosomal vesicle fusion IAGP N RGD:5509061 20220303 MGI PMID:29991750 1316717 Rfx6 regulatory factor X, 6 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1316717 Rfx6 regulatory factor X, 6 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:20148032 1316717 Rfx6 regulatory factor X, 6 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:20148032 1316717 Rfx6 regulatory factor X, 6 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20148032 1316717 Rfx6 regulatory factor X, 6 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:20148032 1316717 Rfx6 regulatory factor X, 6 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:20148032 1316717 Rfx6 regulatory factor X, 6 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1316717 Rfx6 regulatory factor X, 6 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1316717 Rfx6 regulatory factor X, 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20240627 MGI 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0000745 tremors IEA N RGD:5509061 20160421 MGI 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20170629 MGI PMID:26919979 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20170629 MGI PMID:26919979 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20170629 MGI PMID:26919979 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20170629 MGI PMID:26919979 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20201022 MGI 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0009567 mitotic nondisjunction IAGP N RGD:5509061 20170629 MGI PMID:26919979 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20170629 MGI PMID:26919979 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20170629 MGI PMID:26919979 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316719 Smc5 structural maintenance of chromosomes 5 gene MP:0012556 increased cell death IAGP N RGD:5509061 20170629 MGI PMID:26919979 1316724 Arl5c ADP-ribosylation factor-like 5C gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20221215 MGI 1316724 Arl5c ADP-ribosylation factor-like 5C gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20160811 MGI 1316724 Arl5c ADP-ribosylation factor-like 5C gene MP:0000274 enlarged heart IEA N RGD:5509061 20160811 MGI 1316724 Arl5c ADP-ribosylation factor-like 5C gene MP:0001891 hydrocephaly IEA N RGD:5509061 20160811 MGI 1316724 Arl5c ADP-ribosylation factor-like 5C gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20160811 MGI 1316724 Arl5c ADP-ribosylation factor-like 5C gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1316724 Arl5c ADP-ribosylation factor-like 5C gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20231207 MGI 1316724 Arl5c ADP-ribosylation factor-like 5C gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20221215 MGI 1316728 Rad51 RAD51 recombinase gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8943369 1316728 Rad51 RAD51 recombinase gene MP:0001147 small testis IAGP N RGD:5509061 20220721 MGI PMID:35292640 1316728 Rad51 RAD51 recombinase gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220721 MGI PMID:35292640 1316728 Rad51 RAD51 recombinase gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:8943369 1316728 Rad51 RAD51 recombinase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8943369 1316728 Rad51 RAD51 recombinase gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:8943369 1316728 Rad51 RAD51 recombinase gene MP:0001925 male infertility IAGP N RGD:5509061 20220721 MGI PMID:35292640 1316728 Rad51 RAD51 recombinase gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:8943369 1316728 Rad51 RAD51 recombinase gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8943369 1316728 Rad51 RAD51 recombinase gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220721 MGI PMID:35292640 1316728 Rad51 RAD51 recombinase gene MP:0002776 increased Sertoli cell number IAGP N RGD:5509061 20220721 MGI PMID:35292640 1316728 Rad51 RAD51 recombinase gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220721 MGI PMID:35292640 1316728 Rad51 RAD51 recombinase gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220721 MGI PMID:35292640 1316728 Rad51 RAD51 recombinase gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20220721 MGI PMID:35292640 1316728 Rad51 RAD51 recombinase gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20220721 MGI PMID:35292640 1316728 Rad51 RAD51 recombinase gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220721 MGI PMID:35292640 1316728 Rad51 RAD51 recombinase gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20220721 MGI PMID:35292640 1316728 Rad51 RAD51 recombinase gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8692798 1316728 Rad51 RAD51 recombinase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8943369 1316728 Rad51 RAD51 recombinase gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8943369 1316728 Rad51 RAD51 recombinase gene MP:0011191 increased embryonic epiblast cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8943369 1316728 Rad51 RAD51 recombinase gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:8943369 1316728 Rad51 RAD51 recombinase gene MP:0012142 absent amniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:8943369 1316728 Rad51 RAD51 recombinase gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220721 MGI PMID:35292640 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0000339 decreased enterocyte cell number IAGP N RGD:5509061 20141009 MGI PMID:24356953 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141009 MGI PMID:24356953 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001116 small gonad IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141009 MGI PMID:24356953 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141009 MGI PMID:24356953 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001147 small testis IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001155 arrest of spermatogenesis IEA N RGD:5509061 20141009 MGI 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141009 MGI PMID:24356953 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141009 MGI PMID:24356953 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141009 MGI PMID:24356953 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0003578 absent ovary IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0004806 absent germ cells IAGP N RGD:5509061 20141009 MGI PMID:24356953 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0004806 absent germ cells IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0004901 decreased male germ cell number IEA N RGD:5509061 20141009 MGI 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0005431 decreased oocyte number IEA N RGD:5509061 20141009 MGI 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0006428 ectopic Sertoli cells IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0008391 abnormal primordial germ cell morphology IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141009 MGI PMID:24356953 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0008393 absent primordial germ cells IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0008393 absent primordial germ cells IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141009 MGI PMID:24356953 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20141009 MGI PMID:24356953 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141009 MGI PMID:24356953 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0011610 abnormal primordial germ cell apoptosis IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20160526 MGI PMID:24009519 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0012504 increased forebrain apoptosis IAGP N RGD:5509061 20190411 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0030935 increased primordial germ cell apoptosis IAGP N RGD:5509061 20190411 MGI PMID:23463509 1316730 Mad2l2 MAD2 mitotic arrest deficient-like 2 gene MP:0030935 increased primordial germ cell apoptosis IAGP N RGD:5509061 20190411 MGI PMID:24009519 1316731 Rnf214 ring finger protein 214 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20220811 MGI 1316731 Rnf214 ring finger protein 214 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1316731 Rnf214 ring finger protein 214 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1316731 Rnf214 ring finger protein 214 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1316731 Rnf214 ring finger protein 214 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1316734 Ppfibp2 PTPRF interacting protein, binding protein 2 (liprin beta 2) gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20220519 MGI 1316734 Ppfibp2 PTPRF interacting protein, binding protein 2 (liprin beta 2) gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1316734 Ppfibp2 PTPRF interacting protein, binding protein 2 (liprin beta 2) gene MP:0001200 thick skin IEA N RGD:5509061 20220519 MGI 1316734 Ppfibp2 PTPRF interacting protein, binding protein 2 (liprin beta 2) gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20210128 MGI 1316734 Ppfibp2 PTPRF interacting protein, binding protein 2 (liprin beta 2) gene MP:0001304 cataract IEA N RGD:5509061 20240627 MGI 1316734 Ppfibp2 PTPRF interacting protein, binding protein 2 (liprin beta 2) gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20210128 MGI 1316734 Ppfibp2 PTPRF interacting protein, binding protein 2 (liprin beta 2) gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1316734 Ppfibp2 PTPRF interacting protein, binding protein 2 (liprin beta 2) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1316734 Ppfibp2 PTPRF interacting protein, binding protein 2 (liprin beta 2) gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200402 MGI 1316734 Ppfibp2 PTPRF interacting protein, binding protein 2 (liprin beta 2) gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1316736 Tecpr2 tectonin beta-propeller repeat containing 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1316736 Tecpr2 tectonin beta-propeller repeat containing 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20210527 MGI PMID:33218264 1316736 Tecpr2 tectonin beta-propeller repeat containing 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1316736 Tecpr2 tectonin beta-propeller repeat containing 2 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20220519 MGI 1316736 Tecpr2 tectonin beta-propeller repeat containing 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20210527 MGI PMID:33218264 1316736 Tecpr2 tectonin beta-propeller repeat containing 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1316736 Tecpr2 tectonin beta-propeller repeat containing 2 gene MP:0003043 hypoalgesia IEA N RGD:5509061 20220519 MGI 1316736 Tecpr2 tectonin beta-propeller repeat containing 2 gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20210527 MGI PMID:33218264 1316736 Tecpr2 tectonin beta-propeller repeat containing 2 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20210527 MGI PMID:33218264 1316736 Tecpr2 tectonin beta-propeller repeat containing 2 gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20210527 MGI PMID:33218264 1316736 Tecpr2 tectonin beta-propeller repeat containing 2 gene MP:0020954 decreased mechanical nociceptive threshold IEA N RGD:5509061 20220519 MGI 1316736 Tecpr2 tectonin beta-propeller repeat containing 2 gene MP:0020955 increased mechanical nociceptive threshold IAGP N RGD:5509061 20210527 MGI PMID:33218264 1316736 Tecpr2 tectonin beta-propeller repeat containing 2 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20210527 MGI PMID:33218264 1316741 Gpx8 glutathione peroxidase 8 (putative) gene MP:0001194 dermatitis IEA N RGD:5509061 20170406 MGI 1316741 Gpx8 glutathione peroxidase 8 (putative) gene MP:0001222 epidermal hyperplasia IEA N RGD:5509061 20170406 MGI 1316741 Gpx8 glutathione peroxidase 8 (putative) gene MP:0001242 hyperkeratosis IEA N RGD:5509061 20170406 MGI 1316742 Mosmo modulator of smoothened gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0000644 dextrocardia IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0000650 mesocardia IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0000914 exencephaly IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0002764 short tibia IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0002766 situs inversus IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0004133 heterotaxia IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0004320 split sternum IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0010854 lung situs inversus IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316742 Mosmo modulator of smoothened gene MP:0031284 abdominal situs abnormality IAGP N RGD:5509061 20211104 MGI PMID:34486668 1316744 Pif1 PIF1 5'-to-3' DNA helicase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17130244 1316744 Pif1 PIF1 5'-to-3' DNA helicase gene MP:0030928 increased telomere length IAGP N RGD:5509061 20190117 MGI PMID:17130244 1316752 Pmel premelanosome protein gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:21949658 1316752 Pmel premelanosome protein gene MP:0000372 irregular coat pigmentation IEA N RGD:5509061 20111116 MGI 1316752 Pmel premelanosome protein gene MP:0001488 increased startle reflex IEA N RGD:5509061 20181227 MGI 1316752 Pmel premelanosome protein gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:21949658 1316752 Pmel premelanosome protein gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20210826 MGI 1316752 Pmel premelanosome protein gene MP:0008732 reduced hair shaft melanin granule number IEA N RGD:5509061 20111116 MGI 1316752 Pmel premelanosome protein gene MP:0009933 abnormal tail hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21949658 1316752 Pmel premelanosome protein gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1316752 Pmel premelanosome protein gene MP:0010192 abnormal retina melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:21949658 1316752 Pmel premelanosome protein gene MP:0010193 abnormal choroid melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:21949658 1316755 Adam11 a disintegrin and metallopeptidase domain 11 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210520 MGI 1316755 Adam11 a disintegrin and metallopeptidase domain 11 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16504143 1316755 Adam11 a disintegrin and metallopeptidase domain 11 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16504143 1316756 Ccdc32 coiled-coil domain containing 32 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20240523 MGI 1316756 Ccdc32 coiled-coil domain containing 32 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1316758 Sesn1 sestrin 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170810 MGI PMID:28114291 1316758 Sesn1 sestrin 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1316758 Sesn1 sestrin 1 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20170810 MGI PMID:28114291 1316758 Sesn1 sestrin 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1316758 Sesn1 sestrin 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20170810 MGI PMID:28114291 1316758 Sesn1 sestrin 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170810 MGI PMID:28114291 1316758 Sesn1 sestrin 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20170810 MGI PMID:28114291 1316758 Sesn1 sestrin 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1316758 Sesn1 sestrin 1 gene MP:0005655 increased aggression IEA N RGD:5509061 20181227 MGI 1316758 Sesn1 sestrin 1 gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20170810 MGI PMID:28114291 1316758 Sesn1 sestrin 1 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20170810 MGI PMID:28114291 1316758 Sesn1 sestrin 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20240523 MGI 1316758 Sesn1 sestrin 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20170810 MGI PMID:28114291 1316758 Sesn1 sestrin 1 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20170810 MGI PMID:28114291 1316758 Sesn1 sestrin 1 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20170810 MGI PMID:28114291 1316758 Sesn1 sestrin 1 gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20170810 MGI PMID:28114291 1316758 Sesn1 sestrin 1 gene MP:0013762 abnormal effector T cell number IAGP N RGD:5509061 20170810 MGI PMID:28114291 1316762 Fam32a family with sequence similarity 32, member A gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210128 MGI 1316762 Fam32a family with sequence similarity 32, member A gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1316762 Fam32a family with sequence similarity 32, member A gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1316762 Fam32a family with sequence similarity 32, member A gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1316762 Fam32a family with sequence similarity 32, member A gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210826 MGI 1316762 Fam32a family with sequence similarity 32, member A gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1316762 Fam32a family with sequence similarity 32, member A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316762 Fam32a family with sequence similarity 32, member A gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1316762 Fam32a family with sequence similarity 32, member A gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1316765 Klhl6 kelch-like 6 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0000274 enlarged heart IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:16166635 1316765 Klhl6 kelch-like 6 gene MP:0000692 small spleen IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16166635 1316765 Klhl6 kelch-like 6 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0001147 small testis IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16166635 1316765 Klhl6 kelch-like 6 gene MP:0002311 abnormal inspiratory capacity IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:16166635 1316765 Klhl6 kelch-like 6 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0003450 enlarged pancreas IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16166635 1316765 Klhl6 kelch-like 6 gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20190411 MGI 1316765 Klhl6 kelch-like 6 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0005015 increased T cell number IEA N RGD:5509061 20181011 MGI 1316765 Klhl6 kelch-like 6 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16166635 1316765 Klhl6 kelch-like 6 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1316765 Klhl6 kelch-like 6 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190110 MGI 1316765 Klhl6 kelch-like 6 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1316765 Klhl6 kelch-like 6 gene MP:0008082 increased single-positive T cell number IEA N RGD:5509061 20181011 MGI 1316765 Klhl6 kelch-like 6 gene MP:0008167 increased B-1a cell number IEA N RGD:5509061 20190110 MGI 1316765 Klhl6 kelch-like 6 gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20181011 MGI 1316765 Klhl6 kelch-like 6 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:16166635 1316765 Klhl6 kelch-like 6 gene MP:0008211 decreased mature B cell number IEA N RGD:5509061 20141003 MGI 1316765 Klhl6 kelch-like 6 gene MP:0008214 increased immature B cell number IEA N RGD:5509061 20141003 MGI 1316765 Klhl6 kelch-like 6 gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:16166635 1316765 Klhl6 kelch-like 6 gene MP:0010842 decreased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1316765 Klhl6 kelch-like 6 gene MP:0010851 decreased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20190110 MGI 1316765 Klhl6 kelch-like 6 gene MP:0013436 increased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0013763 increased T-helper cell number IEA N RGD:5509061 20240523 MGI 1316765 Klhl6 kelch-like 6 gene MP:0013771 decreased effector memory T-helper cell number IEA N RGD:5509061 20240523 MGI 1316769 Oxa1l oxidase assembly 1-like gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20220811 MGI 1316769 Oxa1l oxidase assembly 1-like gene MP:0003043 hypoalgesia IEA N RGD:5509061 20220519 MGI 1316769 Oxa1l oxidase assembly 1-like gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20220811 MGI 1316769 Oxa1l oxidase assembly 1-like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316769 Oxa1l oxidase assembly 1-like gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1316769 Oxa1l oxidase assembly 1-like gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1316775 Hic1 hypermethylated in cancer 1 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:12539045 1316775 Hic1 hypermethylated in cancer 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:12539045 1316775 Hic1 hypermethylated in cancer 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12539045 1316775 Hic1 hypermethylated in cancer 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12539045 1316775 Hic1 hypermethylated in cancer 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12539045 1316775 Hic1 hypermethylated in cancer 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12539045 1316775 Hic1 hypermethylated in cancer 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21309068 1316775 Hic1 hypermethylated in cancer 1 gene MP:0003104 acrania IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12539045 1316775 Hic1 hypermethylated in cancer 1 gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12539045 1316775 Hic1 hypermethylated in cancer 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0009025 abnormal brain dura mater morphology IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0010348 increased pancreatic islet cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12539045 1316775 Hic1 hypermethylated in cancer 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10655551 1316775 Hic1 hypermethylated in cancer 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21309068 1316775 Hic1 hypermethylated in cancer 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12539045 1316777 Kdm4c lysine (K)-specific demethylase 4C gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20160804 MGI 1316777 Kdm4c lysine (K)-specific demethylase 4C gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20190124 MGI PMID:25340873 1316777 Kdm4c lysine (K)-specific demethylase 4C gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161201 MGI PMID:26248577 1316777 Kdm4c lysine (K)-specific demethylase 4C gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20160804 MGI 1316777 Kdm4c lysine (K)-specific demethylase 4C gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20161201 MGI PMID:26248577 1316777 Kdm4c lysine (K)-specific demethylase 4C gene MP:0005014 increased B cell number IEA N RGD:5509061 20160804 MGI 1316777 Kdm4c lysine (K)-specific demethylase 4C gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170518 MGI PMID:24396064 1316777 Kdm4c lysine (K)-specific demethylase 4C gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20161201 MGI PMID:26248577 1316778 Fmn2 formin 2 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12447394 1316778 Fmn2 formin 2 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:12447394 1316778 Fmn2 formin 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12447394 1316778 Fmn2 formin 2 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:12447394 1316778 Fmn2 formin 2 gene MP:0012737 abnormal primary polar body morphology IAGP N RGD:5509061 20141003 MGI PMID:12447394 1316778 Fmn2 formin 2 gene MP:0014443 impaired polar body extrusion IAGP N RGD:5509061 20240509 MGI PMID:12447394 1316783 Ifngr2 interferon gamma receptor 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9653170 1316783 Ifngr2 interferon gamma receptor 2 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:11714835 1316783 Ifngr2 interferon gamma receptor 2 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:9653170 1316783 Ifngr2 interferon gamma receptor 2 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11714835 1316783 Ifngr2 interferon gamma receptor 2 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:11118001 1316783 Ifngr2 interferon gamma receptor 2 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:9653170 1316783 Ifngr2 interferon gamma receptor 2 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9653170 1316783 Ifngr2 interferon gamma receptor 2 gene MP:0030960 abnormal diapedesis IAGP N RGD:5509061 20190725 MGI PMID:11714835 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15840700 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9449704 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14739216 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20230601 MGI 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16382151 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:16382151 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:12522008 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:9634821 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000757 herniated abdominal wall IEA N RGD:5509061 20141003 MGI 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20230601 MGI 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001512 trunk curl IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15840700 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9449704 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15840700 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:14739216 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:1423604 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:18566402 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20220519 MGI 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16382151 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19856143 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14739216 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:19729608 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0003052 omphalocele IEA N RGD:5509061 20141003 MGI 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0003075 abnormal response to CNS ischemic injury IAGP N RGD:5509061 20141003 MGI PMID:19147818 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:16382151 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:23152628 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23152628 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20141003 MGI 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19147818 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0003924 diaphragmatic hernia IEA N RGD:5509061 20141003 MGI 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0003947 abnormal cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9449704 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:1423604 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0004254 cerebral amyloid angiopathy IAGP N RGD:5509061 20141003 MGI PMID:23152628 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:19729608 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9449704 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14739216 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15840700 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9449704 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14739216 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:12690199 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17038633 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12690199 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:14739216 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17038633 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:14739216 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:15840700 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19729608 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20201231 MGI 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:19147818 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:19147818 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0006134 artery occlusion IAGP N RGD:5509061 20141003 MGI PMID:12690199 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0006265 increased pulse pressure IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:12690199 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0008988 abnormal liver perisinusoidal space morphology IAGP N RGD:5509061 20141003 MGI PMID:16382151 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009137 decreased brown fat lipid droplet number IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12522008 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12690199 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:19729608 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19729608 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:19729608 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0010161 decreased brain cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0010224 abnormal heart ventricle outflow tract morphology IEA N RGD:5509061 20141003 MGI 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0010332 abnormal circulating apolipoprotein level IAGP N RGD:5509061 20141003 MGI PMID:9449704 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0010333 abnormal circulating apolipoprotein E level IAGP N RGD:5509061 20141003 MGI PMID:9449704 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0010470 dilated ascending aorta IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0010574 dilated aorta IAGP N RGD:5509061 20141003 MGI PMID:12690199 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0010659 abdominal aorta aneurysm IAGP N RGD:5509061 20141003 MGI PMID:12690199 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20141003 MGI PMID:12690199 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0011015 decreased body surface temperature IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16382151 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1423604 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19856143 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16382151 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0011575 dilated aorta bulb IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0011749 perivascular fibrosis IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20171228 MGI PMID:24312398 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:15456862 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:17948131 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0012329 increased circulating factor VIII level IAGP N RGD:5509061 20201002 MGI PMID:14739216 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0012329 increased circulating factor VIII level IAGP N RGD:5509061 20201002 MGI PMID:15840700 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0012329 increased circulating factor VIII level IAGP N RGD:5509061 20201015 MGI PMID:12522008 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20211014 MGI PMID:21159977 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0031165 increased circulating von Willebrand factor level IAGP N RGD:5509061 20201015 MGI PMID:12522008 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0031165 increased circulating von Willebrand factor level IAGP N RGD:5509061 20201015 MGI PMID:14739216 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0031165 increased circulating von Willebrand factor level IAGP N RGD:5509061 20201015 MGI PMID:15840700 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0031510 increased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:12690199 1316787 Lrp1 low density lipoprotein receptor-related protein 1 gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:17948131 1316789 Cse1l chromosome segregation 1 like gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11564884 1316789 Cse1l chromosome segregation 1 like gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11564884 1316789 Cse1l chromosome segregation 1 like gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11564884 1316790 Tex56 testis expressed 56 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1316794 Tnrc18 trinucleotide repeat containing 18 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240215 MGI PMID:37938770 1316794 Tnrc18 trinucleotide repeat containing 18 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240215 MGI PMID:37938770 1316798 Fbxo33 F-box protein 33 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1316798 Fbxo33 F-box protein 33 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1316798 Fbxo33 F-box protein 33 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20170105 MGI 1316802 Anxa13 annexin A13 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1316802 Anxa13 annexin A13 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20230601 MGI 1316802 Anxa13 annexin A13 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0000263 absent organized vascular network IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17925232 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0010241 abnormal aortic arch development IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17925232 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16024820 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16024820 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18710940 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150219 MGI PMID:12588986 1316805 Paxip1 PAX interacting (with transcription-activation domain) protein 1 gene MP:0021086 decreased DNA replication IAGP N RGD:5509061 20220310 MGI PMID:12588986 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20201022 MGI 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0001513 limb grasping IEA N RGD:5509061 20210128 MGI 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20190502 MGI 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0005238 increased brain size IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20190502 MGI 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20221215 MGI 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0020337 abnormal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0020512 abnormal dendritic mushroom spine morphology IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0021018 decreased dendritic spine number IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316807 Csmd3 CUB and Sushi multiple domains 3 gene MP:0021090 abnormal dendrite arborization pattern IAGP N RGD:5509061 20220421 MGI PMID:35245678 1316809 Dctn6 dynactin 6 gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20240801 MGI 1316809 Dctn6 dynactin 6 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20191205 MGI 1316809 Dctn6 dynactin 6 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1316809 Dctn6 dynactin 6 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241017 MGI 1316809 Dctn6 dynactin 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316809 Dctn6 dynactin 6 gene MP:0011184 absent embryonic epiblast IEA N RGD:5509061 20191205 MGI 1316809 Dctn6 dynactin 6 gene MP:0011185 absent primitive endoderm IEA N RGD:5509061 20191205 MGI 1316809 Dctn6 dynactin 6 gene MP:0012102 absent trophectoderm IEA N RGD:5509061 20191205 MGI 1316809 Dctn6 dynactin 6 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1316811 Sugt1 SGT1, suppressor of G2 allele of SKP1 (S. cerevisiae) gene MP:0001258 decreased body length IEA N RGD:5509061 20221215 MGI 1316811 Sugt1 SGT1, suppressor of G2 allele of SKP1 (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316811 Sugt1 SGT1, suppressor of G2 allele of SKP1 (S. cerevisiae) gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20151203 MGI PMID:25985210 1316811 Sugt1 SGT1, suppressor of G2 allele of SKP1 (S. cerevisiae) gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1316811 Sugt1 SGT1, suppressor of G2 allele of SKP1 (S. cerevisiae) gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:25985210 1316814 Qsox2 quiescin Q6 sulfhydryl oxidase 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20231207 MGI 1316816 Foxe3 forkhead box E3 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20170330 MGI PMID:26854927 1316816 Foxe3 forkhead box E3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20201022 MGI 1316816 Foxe3 forkhead box E3 gene MP:0001147 small testis IEA N RGD:5509061 20201022 MGI 1316816 Foxe3 forkhead box E3 gene MP:0001288 abnormal lens induction IAGP N RGD:5509061 20170209 MGI PMID:16199865 1316816 Foxe3 forkhead box E3 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20170209 MGI PMID:10652278 1316816 Foxe3 forkhead box E3 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20170209 MGI PMID:109409 1316816 Foxe3 forkhead box E3 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20170209 MGI PMID:6373332 1316816 Foxe3 forkhead box E3 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210826 MGI 1316816 Foxe3 forkhead box E3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20170209 MGI PMID:109409 1316816 Foxe3 forkhead box E3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20170209 MGI PMID:11309658 1316816 Foxe3 forkhead box E3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20170209 MGI PMID:16199865 1316816 Foxe3 forkhead box E3 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20170209 MGI PMID:109409 1316816 Foxe3 forkhead box E3 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20170209 MGI PMID:11309658 1316816 Foxe3 forkhead box E3 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20170209 MGI PMID:22002806 1316816 Foxe3 forkhead box E3 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20170209 MGI PMID:6373332 1316816 Foxe3 forkhead box E3 gene MP:0001304 cataract IAGP N RGD:5509061 20170209 MGI PMID:10652278 1316816 Foxe3 forkhead box E3 gene MP:0001304 cataract IAGP N RGD:5509061 20170209 MGI PMID:11309658 1316816 Foxe3 forkhead box E3 gene MP:0001304 cataract IAGP N RGD:5509061 20170209 MGI PMID:11980846 1316816 Foxe3 forkhead box E3 gene MP:0001304 cataract IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0001306 small lens IAGP N RGD:5509061 20170209 MGI PMID:10652278 1316816 Foxe3 forkhead box E3 gene MP:0001306 small lens IAGP N RGD:5509061 20170209 MGI PMID:109409 1316816 Foxe3 forkhead box E3 gene MP:0001306 small lens IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0001306 small lens IAGP N RGD:5509061 20170209 MGI PMID:6373332 1316816 Foxe3 forkhead box E3 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20170209 MGI PMID:10652278 1316816 Foxe3 forkhead box E3 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20170209 MGI PMID:11980846 1316816 Foxe3 forkhead box E3 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20170209 MGI PMID:109409 1316816 Foxe3 forkhead box E3 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20170209 MGI PMID:11980846 1316816 Foxe3 forkhead box E3 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20170209 MGI PMID:16199865 1316816 Foxe3 forkhead box E3 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20170209 MGI PMID:6373332 1316816 Foxe3 forkhead box E3 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20170209 MGI PMID:109409 1316816 Foxe3 forkhead box E3 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20170209 MGI PMID:11980846 1316816 Foxe3 forkhead box E3 gene MP:0001320 small pupil IAGP N RGD:5509061 20170209 MGI PMID:109409 1316816 Foxe3 forkhead box E3 gene MP:0001320 small pupil IAGP N RGD:5509061 20170209 MGI PMID:16199865 1316816 Foxe3 forkhead box E3 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20170209 MGI PMID:109409 1316816 Foxe3 forkhead box E3 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1316816 Foxe3 forkhead box E3 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20220811 MGI 1316816 Foxe3 forkhead box E3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 1316816 Foxe3 forkhead box E3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20201022 MGI 1316816 Foxe3 forkhead box E3 gene MP:0002579 disorganized secondary lens fibers IAGP N RGD:5509061 20170209 MGI PMID:22002806 1316816 Foxe3 forkhead box E3 gene MP:0002638 abnormal pupillary reflex IAGP N RGD:5509061 20170209 MGI PMID:109409 1316816 Foxe3 forkhead box E3 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20170209 MGI PMID:10652278 1316816 Foxe3 forkhead box E3 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20170209 MGI PMID:109409 1316816 Foxe3 forkhead box E3 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20170209 MGI PMID:16199865 1316816 Foxe3 forkhead box E3 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20170209 MGI PMID:22002806 1316816 Foxe3 forkhead box E3 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20170209 MGI PMID:6373332 1316816 Foxe3 forkhead box E3 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20170209 MGI PMID:10652278 1316816 Foxe3 forkhead box E3 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20170209 MGI PMID:16199865 1316816 Foxe3 forkhead box E3 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20170209 MGI PMID:22002806 1316816 Foxe3 forkhead box E3 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20170330 MGI PMID:26854927 1316816 Foxe3 forkhead box E3 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0004224 absent trabecular meshwork IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0004283 absent cornea endothelium IAGP N RGD:5509061 20170209 MGI PMID:16199865 1316816 Foxe3 forkhead box E3 gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20170330 MGI PMID:26854927 1316816 Foxe3 forkhead box E3 gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20170209 MGI PMID:16199865 1316816 Foxe3 forkhead box E3 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0005204 abnormal canal of Schlemm morphology IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20170209 MGI PMID:16199865 1316816 Foxe3 forkhead box E3 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20170209 MGI PMID:11980846 1316816 Foxe3 forkhead box E3 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20170209 MGI PMID:16199865 1316816 Foxe3 forkhead box E3 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20170209 MGI PMID:109409 1316816 Foxe3 forkhead box E3 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20170209 MGI PMID:16199865 1316816 Foxe3 forkhead box E3 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20170209 MGI PMID:22002806 1316816 Foxe3 forkhead box E3 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20170209 MGI PMID:6373332 1316816 Foxe3 forkhead box E3 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20170330 MGI PMID:26854927 1316816 Foxe3 forkhead box E3 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20170209 MGI PMID:109409 1316816 Foxe3 forkhead box E3 gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0008817 hematoma IAGP N RGD:5509061 20170330 MGI PMID:26854927 1316816 Foxe3 forkhead box E3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20170330 MGI PMID:26854927 1316816 Foxe3 forkhead box E3 gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20170330 MGI PMID:26854927 1316816 Foxe3 forkhead box E3 gene MP:0010255 cortical cataract IAGP N RGD:5509061 20170209 MGI PMID:22002806 1316816 Foxe3 forkhead box E3 gene MP:0010259 anterior polar cataract IAGP N RGD:5509061 20170209 MGI PMID:22002806 1316816 Foxe3 forkhead box E3 gene MP:0010470 dilated ascending aorta IAGP N RGD:5509061 20170330 MGI PMID:26854927 1316816 Foxe3 forkhead box E3 gene MP:0010713 corneal-lenticular stalk IAGP N RGD:5509061 20170209 MGI PMID:11980846 1316816 Foxe3 forkhead box E3 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20170209 MGI PMID:17064680 1316816 Foxe3 forkhead box E3 gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20170209 MGI PMID:16199865 1316816 Foxe3 forkhead box E3 gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:16199865 1316816 Foxe3 forkhead box E3 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:16199865 1316816 Foxe3 forkhead box E3 gene MP:0031345 developmental cataract IAGP N RGD:5509061 20220217 MGI PMID:109409 1316816 Foxe3 forkhead box E3 gene MP:0031345 developmental cataract IAGP N RGD:5509061 20220217 MGI PMID:6373332 1316820 Fech ferrochelatase gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0000611 jaundice IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0001202 skin photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:12149233 1316820 Fech ferrochelatase gene MP:0001202 skin photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0001202 skin photosensitivity IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0001265 decreased body size IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:18780836 1316820 Fech ferrochelatase gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:18780836 1316820 Fech ferrochelatase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0004147 increased porphyrin level IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0004147 increased porphyrin level IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0008387 hypochromic anemia IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0008991 abnormal bile canaliculus morphology IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0010175 leptocytosis IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12149233 1316820 Fech ferrochelatase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20190808 MGI PMID:28093505 1316820 Fech ferrochelatase gene MP:0011188 increased erythrocyte protoporphyrin level IAGP N RGD:5509061 20141003 MGI PMID:18780836 1316820 Fech ferrochelatase gene MP:0011188 increased erythrocyte protoporphyrin level IAGP N RGD:5509061 20141003 MGI PMID:1939658 1316820 Fech ferrochelatase gene MP:0031084 decreased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:1939658 1316822 Pstpip1 proline-serine-threonine phosphatase-interacting protein 1 gene MP:0000162 lordosis IEA N RGD:5509061 20220811 MGI 1316822 Pstpip1 proline-serine-threonine phosphatase-interacting protein 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220811 MGI 1316822 Pstpip1 proline-serine-threonine phosphatase-interacting protein 1 gene MP:0000599 enlarged liver IEA N RGD:5509061 20220811 MGI 1316822 Pstpip1 proline-serine-threonine phosphatase-interacting protein 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220811 MGI 1316822 Pstpip1 proline-serine-threonine phosphatase-interacting protein 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220811 MGI 1316822 Pstpip1 proline-serine-threonine phosphatase-interacting protein 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220811 MGI 1316822 Pstpip1 proline-serine-threonine phosphatase-interacting protein 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220811 MGI 1316822 Pstpip1 proline-serine-threonine phosphatase-interacting protein 1 gene MP:0000716 abnormal immune system cell morphology IEA N RGD:5509061 20111215 MGI 1316822 Pstpip1 proline-serine-threonine phosphatase-interacting protein 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220811 MGI 1316822 Pstpip1 proline-serine-threonine phosphatase-interacting protein 1 gene MP:0002444 abnormal T cell physiology IEA N RGD:5509061 20111215 MGI 1316822 Pstpip1 proline-serine-threonine phosphatase-interacting protein 1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20220811 MGI 1316822 Pstpip1 proline-serine-threonine phosphatase-interacting protein 1 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20220811 MGI 1316822 Pstpip1 proline-serine-threonine phosphatase-interacting protein 1 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20220811 MGI 1316822 Pstpip1 proline-serine-threonine phosphatase-interacting protein 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20221215 MGI 1316822 Pstpip1 proline-serine-threonine phosphatase-interacting protein 1 gene MP:0013763 increased T-helper cell number IEA N RGD:5509061 20220811 MGI 1316824 Rcc1l reculator of chromosome condensation 1 like gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20200310 MGI PMID:28746876 1316824 Rcc1l reculator of chromosome condensation 1 like gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20200310 MGI PMID:28746876 1316824 Rcc1l reculator of chromosome condensation 1 like gene MP:0008495 decreased IgG1 level IEA N RGD:5509061 20160804 MGI 1316824 Rcc1l reculator of chromosome condensation 1 like gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20200310 MGI PMID:28746876 1316824 Rcc1l reculator of chromosome condensation 1 like gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:28746876 1316834 Bloc1s1 biogenesis of lysosomal organelles complex-1, subunit 1 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20170413 MGI PMID:25183008 1316834 Bloc1s1 biogenesis of lysosomal organelles complex-1, subunit 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1316834 Bloc1s1 biogenesis of lysosomal organelles complex-1, subunit 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20170323 MGI PMID:24356961 1316834 Bloc1s1 biogenesis of lysosomal organelles complex-1, subunit 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20170323 MGI PMID:24356961 1316834 Bloc1s1 biogenesis of lysosomal organelles complex-1, subunit 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20170413 MGI PMID:25183008 1316834 Bloc1s1 biogenesis of lysosomal organelles complex-1, subunit 1 gene MP:0008480 absent eye pigmentation IAGP N RGD:5509061 20170413 MGI PMID:25183008 1316834 Bloc1s1 biogenesis of lysosomal organelles complex-1, subunit 1 gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20170413 MGI PMID:25183008 1316834 Bloc1s1 biogenesis of lysosomal organelles complex-1, subunit 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20170413 MGI PMID:25183008 1316834 Bloc1s1 biogenesis of lysosomal organelles complex-1, subunit 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20170323 MGI PMID:24356961 1316834 Bloc1s1 biogenesis of lysosomal organelles complex-1, subunit 1 gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20170323 MGI PMID:24356961 1316840 Rac2 Rac family small GTPase 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10072071 1316840 Rac2 Rac family small GTPase 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10072071 1316840 Rac2 Rac family small GTPase 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20201210 MGI PMID:30723080 1316840 Rac2 Rac family small GTPase 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10072071 1316840 Rac2 Rac family small GTPase 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20201210 MGI PMID:30723080 1316840 Rac2 Rac family small GTPase 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10072071 1316840 Rac2 Rac family small GTPase 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0001606 impaired hematopoiesis IEA N RGD:5509061 20161201 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14564011 1316840 Rac2 Rac family small GTPase 2 gene MP:0001805 decreased IgG level IEA N RGD:5509061 20180222 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0001806 decreased IgM level IEA N RGD:5509061 20150702 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:11581314 1316840 Rac2 Rac family small GTPase 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10072071 1316840 Rac2 Rac family small GTPase 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:10072071 1316840 Rac2 Rac family small GTPase 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:12759446 1316840 Rac2 Rac family small GTPase 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:18068132 1316840 Rac2 Rac family small GTPase 2 gene MP:0002492 decreased IgE level IEA N RGD:5509061 20180222 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0002494 increased IgM level IEA N RGD:5509061 20180222 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:18068132 1316840 Rac2 Rac family small GTPase 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20201210 MGI PMID:30723080 1316840 Rac2 Rac family small GTPase 2 gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20161201 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:14564011 1316840 Rac2 Rac family small GTPase 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20201210 MGI PMID:30723080 1316840 Rac2 Rac family small GTPase 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:14564011 1316840 Rac2 Rac family small GTPase 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20201210 MGI PMID:30723080 1316840 Rac2 Rac family small GTPase 2 gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:18068132 1316840 Rac2 Rac family small GTPase 2 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20201210 MGI PMID:30723080 1316840 Rac2 Rac family small GTPase 2 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IEA N RGD:5509061 20180222 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0005078 abnormal cytotoxic T cell physiology IEA N RGD:5509061 20180222 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11581314 1316840 Rac2 Rac family small GTPase 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18068132 1316840 Rac2 Rac family small GTPase 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20201210 MGI PMID:30723080 1316840 Rac2 Rac family small GTPase 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20180222 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20201210 MGI PMID:30723080 1316840 Rac2 Rac family small GTPase 2 gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:10072071 1316840 Rac2 Rac family small GTPase 2 gene MP:0008168 decreased B-1a cell number IEA N RGD:5509061 20160616 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20160616 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:14564011 1316840 Rac2 Rac family small GTPase 2 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:14564011 1316840 Rac2 Rac family small GTPase 2 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:14564011 1316840 Rac2 Rac family small GTPase 2 gene MP:0008600 decreased circulating interleukin-2 level IAGP N RGD:5509061 20141003 MGI PMID:11581314 1316840 Rac2 Rac family small GTPase 2 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10072071 1316840 Rac2 Rac family small GTPase 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10072071 1316840 Rac2 Rac family small GTPase 2 gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180222 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180222 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20180222 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20180222 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20180222 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0012765 decreased alpha-beta T cell number IAGP N RGD:5509061 20201210 MGI PMID:30723080 1316840 Rac2 Rac family small GTPase 2 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20180222 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20161201 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20150702 MGI 1316840 Rac2 Rac family small GTPase 2 gene MP:0020316 decreased vascular endothelial cell proliferation IAGP N RGD:5509061 20160616 MGI PMID:18068132 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:12732718 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15477599 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15477599 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12393491 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0000239 absent common myeloid progenitor cells IAGP N RGD:5509061 20141003 MGI PMID:15477599 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15477599 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:12393491 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15477599 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:15477599 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15477599 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:15477599 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12393491 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12393491 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12591281 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9271586 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:15477599 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12393491 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15477599 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:12732718 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:12732718 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:12732718 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12393491 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9271586 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:15477599 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:12393491 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12393491 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12732718 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12393491 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12393491 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:12732718 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:12732718 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15477599 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12732718 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:12732718 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15477599 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:12732718 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0010927 decreased osteoid volume IAGP N RGD:5509061 20141003 MGI PMID:12732718 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9271586 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12393491 1316843 Ly6a lymphocyte antigen 6 family member A gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:12732718 1316845 Bphl biphenyl hydrolase like gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20211021 MGI 1316846 Tmem119 transmembrane protein 119 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:22416756 1316846 Tmem119 transmembrane protein 119 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170105 MGI 1316846 Tmem119 transmembrane protein 119 gene MP:0001147 small testis IEA N RGD:5509061 20170105 MGI 1316846 Tmem119 transmembrane protein 119 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22416756 1316846 Tmem119 transmembrane protein 119 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22416756 1316846 Tmem119 transmembrane protein 119 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22416756 1316846 Tmem119 transmembrane protein 119 gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20231026 MGI PMID:37532932 1316846 Tmem119 transmembrane protein 119 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22416756 1316846 Tmem119 transmembrane protein 119 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:22416756 1316846 Tmem119 transmembrane protein 119 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:22416756 1316846 Tmem119 transmembrane protein 119 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:22416756 1316846 Tmem119 transmembrane protein 119 gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:22416756 1316846 Tmem119 transmembrane protein 119 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:22416756 1316846 Tmem119 transmembrane protein 119 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20231026 MGI PMID:37532932 1316848 Nat3 N-acetyltransferase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17403913 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0000440 domed cranium IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0001925 male infertility IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0030966 decreased brain ependyma motile cilium number IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316852 Cfap70 cilia and flagella associated protein 70 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20240229 MGI PMID:37352829 1316853 Mapkbp1 mitogen-activated protein kinase binding protein 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1316853 Mapkbp1 mitogen-activated protein kinase binding protein 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1316853 Mapkbp1 mitogen-activated protein kinase binding protein 1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 1316853 Mapkbp1 mitogen-activated protein kinase binding protein 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1316853 Mapkbp1 mitogen-activated protein kinase binding protein 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1316853 Mapkbp1 mitogen-activated protein kinase binding protein 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20160421 MGI 1316855 Numbl numb-like gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17174898 1316855 Numbl numb-like gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17174898 1316855 Numbl numb-like gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12410312 1316855 Numbl numb-like gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17174898 1316855 Numbl numb-like gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12410312 1316855 Numbl numb-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12410312 1316855 Numbl numb-like gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0002653 abnormal ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:17174898 1316855 Numbl numb-like gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17174898 1316855 Numbl numb-like gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12410312 1316855 Numbl numb-like gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17174898 1316855 Numbl numb-like gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:17174898 1316855 Numbl numb-like gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:12410312 1316855 Numbl numb-like gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:17174898 1316855 Numbl numb-like gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12410312 1316855 Numbl numb-like gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0011724 ectopic cortical neuron IAGP N RGD:5509061 20141003 MGI PMID:14687546 1316855 Numbl numb-like gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:12410312 1316855 Numbl numb-like gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:14687546 1316857 Fbxo4 F-box protein 4 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21911473 1316857 Fbxo4 F-box protein 4 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21911473 1316857 Fbxo4 F-box protein 4 gene MP:0002047 increased hepatic hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:21911473 1316857 Fbxo4 F-box protein 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21911473 1316857 Fbxo4 F-box protein 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22124152 1316857 Fbxo4 F-box protein 4 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:21911473 1316857 Fbxo4 F-box protein 4 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21911473 1316857 Fbxo4 F-box protein 4 gene MP:0009222 increased uterus tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21911473 1316857 Fbxo4 F-box protein 4 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21911473 1316857 Fbxo4 F-box protein 4 gene MP:0009439 increased myeloid sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21911473 1316857 Fbxo4 F-box protein 4 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21911473 1316857 Fbxo4 F-box protein 4 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21911473 1316857 Fbxo4 F-box protein 4 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:21911473 1316857 Fbxo4 F-box protein 4 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21911473 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:23160237 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15322545 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20201022 MGI 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:15322545 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20200514 MGI 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23160237 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20201022 MGI 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0002188 small heart IEA N RGD:5509061 20201022 MGI 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23160237 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210128 MGI 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20161222 MGI PMID:26216965 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16170314 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:16170314 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:23160237 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15322545 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0008581 disorganized photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20161222 MGI PMID:26216965 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15322545 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0011059 abnormal ependyma motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15322545 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16170314 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0011281 abnormal olfactory epithelium cilium morphology IAGP N RGD:5509061 20160407 MGI PMID:15322545 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:18032602 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20160218 MGI PMID:23160237 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20161117 MGI PMID:23160237 1316859 Bbs1 Bardet-Biedl syndrome 1 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20191128 MGI PMID:31479441 1316862 Hoxc5 homeobox C5 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316862 Hoxc5 homeobox C5 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316862 Hoxc5 homeobox C5 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316862 Hoxc5 homeobox C5 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316862 Hoxc5 homeobox C5 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316862 Hoxc5 homeobox C5 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316862 Hoxc5 homeobox C5 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316862 Hoxc5 homeobox C5 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316862 Hoxc5 homeobox C5 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316862 Hoxc5 homeobox C5 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316862 Hoxc5 homeobox C5 gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316862 Hoxc5 homeobox C5 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316862 Hoxc5 homeobox C5 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316862 Hoxc5 homeobox C5 gene MP:0012668 absent sternal manubrium IAGP N RGD:5509061 20141003 MGI PMID:17626057 1316864 Efhd2 EF hand domain containing 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20160225 MGI PMID:25092375 1316864 Efhd2 EF hand domain containing 2 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20160225 MGI PMID:25092375 1316864 Efhd2 EF hand domain containing 2 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20160225 MGI PMID:25133820 1316864 Efhd2 EF hand domain containing 2 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20160225 MGI PMID:25092375 1316864 Efhd2 EF hand domain containing 2 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20160225 MGI PMID:25092375 1316864 Efhd2 EF hand domain containing 2 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20160225 MGI PMID:25092375 1316864 Efhd2 EF hand domain containing 2 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20160225 MGI PMID:25092375 1316864 Efhd2 EF hand domain containing 2 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20160225 MGI PMID:25092375 1316864 Efhd2 EF hand domain containing 2 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20160225 MGI PMID:25092375 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20161013 MGI PMID:25637356 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0000120 malocclusion IAGP N RGD:5509061 20161013 MGI PMID:25637356 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20181227 MGI 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:23892084 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:15774718 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:20005824 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001314 cornea opacity IEA N RGD:5509061 20160421 MGI 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:19896504 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19896504 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20005824 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20150827 MGI PMID:19896504 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19896504 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20005824 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:19896504 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:20005824 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20141003 MGI PMID:20005824 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20161013 MGI PMID:25637356 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:23175442 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:23175442 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:20005824 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:15774718 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20161013 MGI PMID:25637356 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:23175442 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:23175442 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:23175442 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23892084 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23892084 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:19896504 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20160421 MGI 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:19896504 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:20005824 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20201022 MGI 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:23175442 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20161013 MGI PMID:25637356 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:19896504 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:23175442 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0003842 abnormal metopic suture morphology IAGP N RGD:5509061 20161013 MGI PMID:25637356 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160421 MGI 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15774718 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23175442 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160421 MGI 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20170105 MGI 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20181227 MGI 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:23175442 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20161013 MGI PMID:25637356 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009121 increased white fat cell lipid droplet size IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009137 decreased brown fat lipid droplet number IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20161013 MGI PMID:25637356 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20161013 MGI PMID:25637356 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:20005824 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23175442 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:20005824 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23175442 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20161013 MGI PMID:25637356 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20161013 MGI PMID:25637356 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20005824 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:23175442 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23175442 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23892084 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0010614 abnormal mitral valve cusp morphology IAGP N RGD:5509061 20141003 MGI PMID:23892084 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0010625 absent tricuspid valve cusps IAGP N RGD:5509061 20141003 MGI PMID:23892084 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20161013 MGI PMID:25637356 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20161013 MGI PMID:25637356 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23892084 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15774718 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20161013 MGI PMID:25637356 1316869 Ehmt1 euchromatic histone methyltransferase 1 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20180111 MGI PMID:24196706 1316871 Thap1 THAP domain containing, apoptosis associated protein 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20180118 MGI PMID:26376866 1316871 Thap1 THAP domain containing, apoptosis associated protein 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20180118 MGI PMID:26376866 1316871 Thap1 THAP domain containing, apoptosis associated protein 1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20190502 MGI 1316871 Thap1 THAP domain containing, apoptosis associated protein 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20180118 MGI PMID:26376866 1316871 Thap1 THAP domain containing, apoptosis associated protein 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20180118 MGI PMID:26376866 1316871 Thap1 THAP domain containing, apoptosis associated protein 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1316871 Thap1 THAP domain containing, apoptosis associated protein 1 gene MP:0009980 abnormal cerebellum dentate nucleus morphology IAGP N RGD:5509061 20180118 MGI PMID:26376866 1316871 Thap1 THAP domain containing, apoptosis associated protein 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20221215 MGI 1316871 Thap1 THAP domain containing, apoptosis associated protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180118 MGI PMID:26376866 1316871 Thap1 THAP domain containing, apoptosis associated protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180118 MGI PMID:26376866 1316871 Thap1 THAP domain containing, apoptosis associated protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316871 Thap1 THAP domain containing, apoptosis associated protein 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20180118 MGI PMID:26376866 1316871 Thap1 THAP domain containing, apoptosis associated protein 1 gene MP:0011877 absent liver IAGP N RGD:5509061 20180118 MGI PMID:26376866 1316871 Thap1 THAP domain containing, apoptosis associated protein 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1316873 Flii flightless I actin binding protein gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190808 MGI 1316873 Flii flightless I actin binding protein gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11971982 1316873 Flii flightless I actin binding protein gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1316873 Flii flightless I actin binding protein gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:17326236 1316873 Flii flightless I actin binding protein gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1316873 Flii flightless I actin binding protein gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11971982 1316873 Flii flightless I actin binding protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316873 Flii flightless I actin binding protein gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1316877 Lin28a lin-28 homolog A gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23378032 1316877 Lin28a lin-28 homolog A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23378032 1316877 Lin28a lin-28 homolog A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:23378032 1316877 Lin28a lin-28 homolog A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:23378032 1316877 Lin28a lin-28 homolog A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23378032 1316877 Lin28a lin-28 homolog A gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:23378032 1316877 Lin28a lin-28 homolog A gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23378032 1316877 Lin28a lin-28 homolog A gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1316877 Lin28a lin-28 homolog A gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:23378032 1316877 Lin28a lin-28 homolog A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23378032 1316877 Lin28a lin-28 homolog A gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:23378032 1316877 Lin28a lin-28 homolog A gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:23378032 1316877 Lin28a lin-28 homolog A gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:23378032 1316877 Lin28a lin-28 homolog A gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21962509 1316877 Lin28a lin-28 homolog A gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21962509 1316877 Lin28a lin-28 homolog A gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:23378032 1316877 Lin28a lin-28 homolog A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:23378032 1316877 Lin28a lin-28 homolog A gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:20512147 1316877 Lin28a lin-28 homolog A gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20512147 1316877 Lin28a lin-28 homolog A gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316877 Lin28a lin-28 homolog A gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:23378032 1316877 Lin28a lin-28 homolog A gene MP:0012681 collapsed brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:23666760 1316885 Arel1 apoptosis resistant E3 ubiquitin protein ligase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1316885 Arel1 apoptosis resistant E3 ubiquitin protein ligase 1 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20200402 MGI PMID:31578312 1316885 Arel1 apoptosis resistant E3 ubiquitin protein ligase 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1316885 Arel1 apoptosis resistant E3 ubiquitin protein ligase 1 gene MP:0020001 decreased response to antigen IAGP N RGD:5509061 20200402 MGI PMID:31578312 1316890 Ifitm1 interferon induced transmembrane protein 1 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:23115618 1316890 Ifitm1 interferon induced transmembrane protein 1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20200402 MGI 1316890 Ifitm1 interferon induced transmembrane protein 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:23115618 1316890 Ifitm1 interferon induced transmembrane protein 1 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:23115618 1316890 Ifitm1 interferon induced transmembrane protein 1 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:23115618 1316890 Ifitm1 interferon induced transmembrane protein 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23115618 1316890 Ifitm1 interferon induced transmembrane protein 1 gene MP:0003858 enhanced coordination IEA N RGD:5509061 20141003 MGI 1316890 Ifitm1 interferon induced transmembrane protein 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 1316890 Ifitm1 interferon induced transmembrane protein 1 gene MP:0004357 long tibia IEA N RGD:5509061 20211021 MGI 1316890 Ifitm1 interferon induced transmembrane protein 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23115618 1316890 Ifitm1 interferon induced transmembrane protein 1 gene MP:0005180 abnormal circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:23115618 1316890 Ifitm1 interferon induced transmembrane protein 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:23115618 1316899 Hexb hexosaminidase B gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9184660 1316899 Hexb hexosaminidase B gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9184660 1316899 Hexb hexosaminidase B gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9184660 1316899 Hexb hexosaminidase B gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20181227 MGI 1316899 Hexb hexosaminidase B gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:12617783 1316899 Hexb hexosaminidase B gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9184660 1316899 Hexb hexosaminidase B gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:7550345 1316899 Hexb hexosaminidase B gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7550345 1316899 Hexb hexosaminidase B gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23028353 1316899 Hexb hexosaminidase B gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:8789434 1316899 Hexb hexosaminidase B gene MP:0000745 tremors IAGP N RGD:5509061 20160929 MGI PMID:27534441 1316899 Hexb hexosaminidase B gene MP:0000745 tremors IAGP N RGD:5509061 20210304 MGI PMID:31547903 1316899 Hexb hexosaminidase B gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:8789434 1316899 Hexb hexosaminidase B gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:8789434 1316899 Hexb hexosaminidase B gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10021458 1316899 Hexb hexosaminidase B gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:14722612 1316899 Hexb hexosaminidase B gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10021458 1316899 Hexb hexosaminidase B gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:9184660 1316899 Hexb hexosaminidase B gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9184660 1316899 Hexb hexosaminidase B gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:8789434 1316899 Hexb hexosaminidase B gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:10021458 1316899 Hexb hexosaminidase B gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23028353 1316899 Hexb hexosaminidase B gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 1316899 Hexb hexosaminidase B gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10021458 1316899 Hexb hexosaminidase B gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:8789434 1316899 Hexb hexosaminidase B gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:14722612 1316899 Hexb hexosaminidase B gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10021458 1316899 Hexb hexosaminidase B gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:14722612 1316899 Hexb hexosaminidase B gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:7550345 1316899 Hexb hexosaminidase B gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:7550345 1316899 Hexb hexosaminidase B gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1316899 Hexb hexosaminidase B gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:14722612 1316899 Hexb hexosaminidase B gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:14722612 1316899 Hexb hexosaminidase B gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:15155903 1316899 Hexb hexosaminidase B gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10021458 1316899 Hexb hexosaminidase B gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:23028353 1316899 Hexb hexosaminidase B gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:14722612 1316899 Hexb hexosaminidase B gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20141003 MGI PMID:8789434 1316899 Hexb hexosaminidase B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:23028353 1316899 Hexb hexosaminidase B gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:7550345 1316899 Hexb hexosaminidase B gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10021458 1316899 Hexb hexosaminidase B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14722612 1316899 Hexb hexosaminidase B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15155903 1316899 Hexb hexosaminidase B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23028353 1316899 Hexb hexosaminidase B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8789434 1316899 Hexb hexosaminidase B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:9184660 1316899 Hexb hexosaminidase B gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20210304 MGI PMID:31547903 1316899 Hexb hexosaminidase B gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:23028353 1316899 Hexb hexosaminidase B gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:12617783 1316899 Hexb hexosaminidase B gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:9645704 1316899 Hexb hexosaminidase B gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20210304 MGI PMID:31547903 1316899 Hexb hexosaminidase B gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:14722612 1316899 Hexb hexosaminidase B gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:7550345 1316899 Hexb hexosaminidase B gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:10021458 1316899 Hexb hexosaminidase B gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14722612 1316899 Hexb hexosaminidase B gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:12617783 1316899 Hexb hexosaminidase B gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:9645704 1316899 Hexb hexosaminidase B gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20141003 MGI PMID:15155903 1316899 Hexb hexosaminidase B gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10021458 1316899 Hexb hexosaminidase B gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:7550345 1316899 Hexb hexosaminidase B gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 1316899 Hexb hexosaminidase B gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:8789434 1316899 Hexb hexosaminidase B gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:9184660 1316899 Hexb hexosaminidase B gene MP:0003807 camptodactyly IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0004100 abnormal spinal cord interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23028353 1316899 Hexb hexosaminidase B gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:23028353 1316899 Hexb hexosaminidase B gene MP:0004676 wide ribs IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0004728 abnormal efferent ductules of testis morphology IAGP N RGD:5509061 20141003 MGI PMID:9645704 1316899 Hexb hexosaminidase B gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:7550345 1316899 Hexb hexosaminidase B gene MP:0004928 increased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:9645704 1316899 Hexb hexosaminidase B gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20210304 MGI PMID:31547903 1316899 Hexb hexosaminidase B gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:23028353 1316899 Hexb hexosaminidase B gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:8789434 1316899 Hexb hexosaminidase B gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20181227 MGI 1316899 Hexb hexosaminidase B gene MP:0005505 thrombocytosis IEA N RGD:5509061 20210128 MGI 1316899 Hexb hexosaminidase B gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14722612 1316899 Hexb hexosaminidase B gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:15155903 1316899 Hexb hexosaminidase B gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:14722612 1316899 Hexb hexosaminidase B gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15155903 1316899 Hexb hexosaminidase B gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20211021 MGI 1316899 Hexb hexosaminidase B gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23028353 1316899 Hexb hexosaminidase B gene MP:0009249 enlarged caput epididymis IAGP N RGD:5509061 20141003 MGI PMID:9645704 1316899 Hexb hexosaminidase B gene MP:0009256 enlarged corpus epididymis IAGP N RGD:5509061 20141003 MGI PMID:9645704 1316899 Hexb hexosaminidase B gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10021458 1316899 Hexb hexosaminidase B gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:14722612 1316899 Hexb hexosaminidase B gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20181227 MGI 1316899 Hexb hexosaminidase B gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0011473 increased urine glycosaminoglycan level IAGP N RGD:5509061 20141003 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0012504 increased forebrain apoptosis IAGP N RGD:5509061 20160428 MGI PMID:14722612 1316899 Hexb hexosaminidase B gene MP:0020851 abnormal vacuole morphology IAGP N RGD:5509061 20210304 MGI PMID:31547903 1316899 Hexb hexosaminidase B gene MP:0030189 broad snout IAGP N RGD:5509061 20171019 MGI PMID:8896570 1316899 Hexb hexosaminidase B gene MP:0030262 frontal bossing IAGP N RGD:5509061 20171026 MGI PMID:8896570 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0000277 abnormal heart shape IEA N RGD:5509061 20210520 MGI 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20220811 MGI 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20201022 MGI 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0001260 increased body weight IAGP N RGD:5509061 20241031 MGI PMID:38574733 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20241031 MGI PMID:38574733 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210826 MGI 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20201022 MGI 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20201022 MGI 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0004155 decreased susceptibility to induced pancreatitis IAGP N RGD:5509061 20241031 MGI PMID:38574733 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0004247 small pancreas IAGP N RGD:5509061 20241031 MGI PMID:38574733 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20201022 MGI 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20241031 MGI PMID:38574733 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316900 Ube2f ubiquitin-conjugating enzyme E2F (putative) gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1316902 Trim13 tripartite motif-containing 13 gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20220519 MGI 1316902 Trim13 tripartite motif-containing 13 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220519 MGI 1316902 Trim13 tripartite motif-containing 13 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20210826 MGI 1316902 Trim13 tripartite motif-containing 13 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1316902 Trim13 tripartite motif-containing 13 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20200514 MGI 1316902 Trim13 tripartite motif-containing 13 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1316902 Trim13 tripartite motif-containing 13 gene MP:0002637 small uterus IEA N RGD:5509061 20220519 MGI 1316902 Trim13 tripartite motif-containing 13 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20220519 MGI 1316902 Trim13 tripartite motif-containing 13 gene MP:0008548 abnormal circulating interferon level IAGP N RGD:5509061 20190117 MGI PMID:25008915 1316902 Trim13 tripartite motif-containing 13 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20190117 MGI PMID:25008915 1316902 Trim13 tripartite motif-containing 13 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20190117 MGI PMID:25008915 1316902 Trim13 tripartite motif-containing 13 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1316902 Trim13 tripartite motif-containing 13 gene MP:0031039 decreased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:25008915 1316903 Raver2 ribonucleoprotein, PTB-binding 2 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1316903 Raver2 ribonucleoprotein, PTB-binding 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:9660954 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17425408 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9660954 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:9660953 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:9660954 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17425408 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:9660953 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:9660954 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10700192 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17425408 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9660953 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9660954 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17425408 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9660953 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:9660953 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:9660954 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:9660953 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:9660954 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10700192 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:9660953 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10700192 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:17425408 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:9660953 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:9660954 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:22549958 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:9660953 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:9660954 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:9660953 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:9660953 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10700192 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:9660953 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:9660954 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:17425408 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:9660953 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23318132 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:17425408 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17425408 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17425408 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:9660953 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:9660954 1316905 Dmc1 DNA meiotic recombinase 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:21478856 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17643102 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0000478 delayed intestine development IAGP N RGD:5509061 20141003 MGI PMID:9288097 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:9288097 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:9288097 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17643102 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:9288097 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20210218 MGI PMID:17643102 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9288097 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:17643102 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17643102 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:16484321 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:16484321 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9288097 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17643102 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17643102 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0001889 delayed brain development IAGP N RGD:5509061 20141003 MGI PMID:9288097 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16484321 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:17643102 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9288097 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17643102 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:9288097 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:17643102 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16484321 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17643102 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9288097 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16484321 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17442273 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:17643102 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:17643102 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:17643102 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0010952 abnormal fatty acid beta-oxidation IAGP N RGD:5509061 20141003 MGI PMID:17442273 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9288097 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0011634 abnormal mitochondrial inner membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:15732085 1316907 Pex5 peroxisomal biogenesis factor 5 gene MP:0031204 hindlimb paresis IAGP N RGD:5509061 20210218 MGI PMID:17643102 1316909 Stard7 StAR related lipid transfer domain containing 7 gene MP:0001194 dermatitis IAGP N RGD:5509061 20180111 MGI PMID:25980009 1316909 Stard7 StAR related lipid transfer domain containing 7 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20180111 MGI PMID:25980009 1316909 Stard7 StAR related lipid transfer domain containing 7 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20180111 MGI PMID:25980009 1316909 Stard7 StAR related lipid transfer domain containing 7 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20180111 MGI PMID:25980009 1316909 Stard7 StAR related lipid transfer domain containing 7 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210520 MGI 1316909 Stard7 StAR related lipid transfer domain containing 7 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20180111 MGI PMID:25980009 1316909 Stard7 StAR related lipid transfer domain containing 7 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20180111 MGI PMID:25980009 1316909 Stard7 StAR related lipid transfer domain containing 7 gene MP:0013648 increased CD11b-high dendritic cell number IAGP N RGD:5509061 20180111 MGI PMID:25980009 1316909 Stard7 StAR related lipid transfer domain containing 7 gene MP:0014026 abnormal respiratory epithelial transmembrane transport IAGP N RGD:5509061 20180111 MGI PMID:25980009 1316909 Stard7 StAR related lipid transfer domain containing 7 gene MP:0014032 abnormal mucous gland morphology IAGP N RGD:5509061 20180111 MGI PMID:25980009 1316911 Ube2m ubiquitin-conjugating enzyme E2M gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1316911 Ube2m ubiquitin-conjugating enzyme E2M gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191128 MGI 1316911 Ube2m ubiquitin-conjugating enzyme E2M gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191128 MGI 1316911 Ube2m ubiquitin-conjugating enzyme E2M gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1316911 Ube2m ubiquitin-conjugating enzyme E2M gene MP:0003886 abnormal embryonic epiblast morphology IEA N RGD:5509061 20191128 MGI 1316911 Ube2m ubiquitin-conjugating enzyme E2M gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1316911 Ube2m ubiquitin-conjugating enzyme E2M gene MP:0009331 absent primitive node IEA N RGD:5509061 20191128 MGI 1316911 Ube2m ubiquitin-conjugating enzyme E2M gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20181220 MGI PMID:25581363 1316911 Ube2m ubiquitin-conjugating enzyme E2M gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1316911 Ube2m ubiquitin-conjugating enzyme E2M gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316911 Ube2m ubiquitin-conjugating enzyme E2M gene MP:0012724 absent head fold IEA N RGD:5509061 20191128 MGI 1316911 Ube2m ubiquitin-conjugating enzyme E2M gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20170105 MGI 1316913 Rabl6 RAB, member RAS oncogene family-like 6 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20231207 MGI 1316913 Rabl6 RAB, member RAS oncogene family-like 6 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20231207 MGI 1316913 Rabl6 RAB, member RAS oncogene family-like 6 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1316915 Yars1 tyrosyl-tRNA synthetase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1316915 Yars1 tyrosyl-tRNA synthetase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20231207 MGI 1316915 Yars1 tyrosyl-tRNA synthetase 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20231207 MGI 1316915 Yars1 tyrosyl-tRNA synthetase 1 gene MP:0020845 abnormal DNA-templated transcription IAGP N RGD:5509061 20220407 MGI PMID:34516839 1316917 Adsl adenylosuccinate lyase gene MP:0001297 microphthalmia IEA N RGD:5509061 20190502 MGI 1316917 Adsl adenylosuccinate lyase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1316917 Adsl adenylosuccinate lyase gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20161201 MGI 1316917 Adsl adenylosuccinate lyase gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1316917 Adsl adenylosuccinate lyase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316917 Adsl adenylosuccinate lyase gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20210722 MGI PMID:33942714 1316917 Adsl adenylosuccinate lyase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0000071 axial skeleton hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20812917 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0000120 malocclusion IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0000161 scoliosis IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:20812917 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:21148564 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:20812917 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:20812917 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20812917 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20141003 MGI 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21148564 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:21148564 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:20812917 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:20812917 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:21148564 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:21148564 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0004351 short humerus IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:20812917 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:21148564 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:21148564 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0008797 facial cleft IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0008910 thin long bone epiphysis IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:21148564 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0009897 decreased maxillary shelf size IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0011475 abnormal glycosaminoglycan level IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0011650 abnormal cornea stroma collagen fibril morphology IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20180308 MGI PMID:29287114 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0030066 short face IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0030132 periodontium inflammation IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0030178 abnormal scalp morphology IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0030198 nasal septum hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0030245 round head IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0030445 abnormal sphenooccipital synchondrosis IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0030584 skin atrophy IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0030797 joint laxity IAGP N RGD:5509061 20221006 MGI PMID:30459452 1316918 Csgalnact1 chondroitin sulfate N-acetylgalactosaminyltransferase 1 gene MP:0031450 nasal cartilage hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:30459452 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:17470284 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000553 absent radius IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000561 adactyly IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20151112 MGI PMID:23358455 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17470284 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17470284 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17470284 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000914 exencephaly IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:17470284 1316920 Sp8 trans-acting transcription factor 8 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20150305 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 1316920 Sp8 trans-acting transcription factor 8 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 1316920 Sp8 trans-acting transcription factor 8 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0002728 absent tibia IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0002728 absent tibia IAGP N RGD:5509061 20151112 MGI PMID:23358455 1316920 Sp8 trans-acting transcription factor 8 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:17470284 1316920 Sp8 trans-acting transcription factor 8 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:16476661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0002764 short tibia IAGP N RGD:5509061 20151112 MGI PMID:23358455 1316920 Sp8 trans-acting transcription factor 8 gene MP:0002765 short fibula IAGP N RGD:5509061 20151112 MGI PMID:23358455 1316920 Sp8 trans-acting transcription factor 8 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0003124 hypospadia IAGP N RGD:5509061 20151112 MGI PMID:23358455 1316920 Sp8 trans-acting transcription factor 8 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17470284 1316920 Sp8 trans-acting transcription factor 8 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:17470284 1316920 Sp8 trans-acting transcription factor 8 gene MP:0003315 abnormal perineum morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 1316920 Sp8 trans-acting transcription factor 8 gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0004383 absent interparietal bone IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0004419 absent parietal bone IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0004444 small supraoccipital bone IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0004540 small maxilla IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0004653 absent caudal vertebrae IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0004656 absent sacral vertebrae IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0004870 small premaxilla IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:17470284 1316920 Sp8 trans-acting transcription factor 8 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:17470284 1316920 Sp8 trans-acting transcription factor 8 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0005430 absent fibula IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0005430 absent fibula IAGP N RGD:5509061 20151112 MGI PMID:23358455 1316920 Sp8 trans-acting transcription factor 8 gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17470284 1316920 Sp8 trans-acting transcription factor 8 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0006306 abnormal nasal pit morphology IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:17470284 1316920 Sp8 trans-acting transcription factor 8 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17470284 1316920 Sp8 trans-acting transcription factor 8 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20141003 MGI PMID:17470284 1316920 Sp8 trans-acting transcription factor 8 gene MP:0009053 abnormal anal canal morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 1316920 Sp8 trans-acting transcription factor 8 gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0009946 abnormal olfactory bulb layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16476661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0009947 abnormal olfactory bulb external plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16476661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16476661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0009950 abnormal olfactory bulb internal plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16476661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17470284 1316920 Sp8 trans-acting transcription factor 8 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0011771 abnormal genital tubercle morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 1316920 Sp8 trans-acting transcription factor 8 gene MP:0011772 genital tubercle hypoplasia IAGP N RGD:5509061 20151112 MGI PMID:23358455 1316920 Sp8 trans-acting transcription factor 8 gene MP:0012260 encephalomeningocele IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0012707 incomplete caudal neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:14526104 1316920 Sp8 trans-acting transcription factor 8 gene MP:0012760 decreased cranial neural crest cell proliferation IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0012761 increased cranial neural crest cell apoptosis IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0013164 abnormal forelimb bud morphology IAGP N RGD:5509061 20150528 MGI PMID:14597661 1316920 Sp8 trans-acting transcription factor 8 gene MP:0013199 increased head mesenchyme apoptosis IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0030190 small snout IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316920 Sp8 trans-acting transcription factor 8 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230309 MGI PMID:23872235 1316922 Catsper2 cation channel, sperm associated 2 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:14657366 1316922 Catsper2 cation channel, sperm associated 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14657366 1316922 Catsper2 cation channel, sperm associated 2 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:17227845 1316922 Catsper2 cation channel, sperm associated 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:14657366 1316922 Catsper2 cation channel, sperm associated 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17227845 1316922 Catsper2 cation channel, sperm associated 2 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:17227845 1316922 Catsper2 cation channel, sperm associated 2 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:14657366 1316926 Rhoh ras homolog family member H gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17028588 1316926 Rhoh ras homolog family member H gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17028588 1316926 Rhoh ras homolog family member H gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19124738 1316926 Rhoh ras homolog family member H gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17028588 1316926 Rhoh ras homolog family member H gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17028588 1316926 Rhoh ras homolog family member H gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:19124738 1316926 Rhoh ras homolog family member H gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316926 Rhoh ras homolog family member H gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:19124738 1316926 Rhoh ras homolog family member H gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:17119112 1316928 Borcs5 BLOC-1 related complex subunit 5 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20210401 MGI PMID:32553155 1316928 Borcs5 BLOC-1 related complex subunit 5 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 1316928 Borcs5 BLOC-1 related complex subunit 5 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20210401 MGI PMID:32553155 1316928 Borcs5 BLOC-1 related complex subunit 5 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20210401 MGI PMID:32553155 1316928 Borcs5 BLOC-1 related complex subunit 5 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20210401 MGI PMID:32553155 1316928 Borcs5 BLOC-1 related complex subunit 5 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20210401 MGI PMID:32553155 1316928 Borcs5 BLOC-1 related complex subunit 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1316930 Kel Kell blood group gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:19544475 1316930 Kel Kell blood group gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19544475 1316930 Kel Kell blood group gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19544475 1316930 Kel Kell blood group gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:19544475 1316930 Kel Kell blood group gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:19544475 1316930 Kel Kell blood group gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:23122227 1316930 Kel Kell blood group gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20151224 MGI PMID:23122227 1316930 Kel Kell blood group gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:24405768 1316930 Kel Kell blood group gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:19544475 1316930 Kel Kell blood group gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:24405768 1316930 Kel Kell blood group gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:19544475 1316930 Kel Kell blood group gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:19544475 1316930 Kel Kell blood group gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20151224 MGI PMID:23122227 1316930 Kel Kell blood group gene MP:0008850 increased hemoglobin concentration distribution width IAGP N RGD:5509061 20141003 MGI PMID:19544475 1316930 Kel Kell blood group gene MP:0008850 increased hemoglobin concentration distribution width IAGP N RGD:5509061 20141003 MGI PMID:23122227 1316930 Kel Kell blood group gene MP:0008954 abnormal cellular hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19544475 1316930 Kel Kell blood group gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:24405768 1316930 Kel Kell blood group gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:24405768 1316930 Kel Kell blood group gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:19544475 1316930 Kel Kell blood group gene MP:0010511 shortened PR interval IAGP N RGD:5509061 20141003 MGI PMID:19544475 1316930 Kel Kell blood group gene MP:0010738 abnormal internode morphology IAGP N RGD:5509061 20141003 MGI PMID:19544475 1316930 Kel Kell blood group gene MP:0010738 abnormal internode morphology IAGP N RGD:5509061 20141003 MGI PMID:24405768 1316930 Kel Kell blood group gene MP:0011730 increased myelin sheath thickness IAGP N RGD:5509061 20141003 MGI PMID:19544475 1316930 Kel Kell blood group gene MP:0011730 increased myelin sheath thickness IAGP N RGD:5509061 20141003 MGI PMID:24405768 1316930 Kel Kell blood group gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20141003 MGI PMID:24405768 1316930 Kel Kell blood group gene MP:0011913 abnormal reticulocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23122227 1316930 Kel Kell blood group gene MP:0011954 shortened PQ interval IAGP N RGD:5509061 20141003 MGI PMID:19544475 1316930 Kel Kell blood group gene MP:0012365 increased erythrocyte sodium level IAGP N RGD:5509061 20141003 MGI PMID:23122227 1316930 Kel Kell blood group gene MP:0012367 decreased erythrocyte magnesium level IAGP N RGD:5509061 20141003 MGI PMID:23122227 1316930 Kel Kell blood group gene MP:0012370 decreased erythrocyte potassium level IAGP N RGD:5509061 20141003 MGI PMID:23122227 1316930 Kel Kell blood group gene MP:0012372 abnormal erythrocyte ion content IAGP N RGD:5509061 20141003 MGI PMID:23122227 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0000111 cleft palate IAGP N RGD:5509061 20221006 MGI PMID:35212626 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0000160 kyphosis IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20160428 MGI PMID:23452852 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0000547 short limbs IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:23967333 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:20729857 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:20729857 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:23103168 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0001575 cyanosis IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20160428 MGI PMID:23452852 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20729857 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23967333 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20160428 MGI PMID:23452852 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0003154 abnormal soft palate morphology IAGP N RGD:5509061 20221006 MGI PMID:35212626 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:23103168 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0004351 short humerus IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:20729857 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20221006 MGI PMID:35212626 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:23967333 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:20729857 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20221006 MGI PMID:35212626 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20221006 MGI PMID:35212626 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0009896 palatine bone horizontal plate hypoplasia IAGP N RGD:5509061 20221006 MGI PMID:35212626 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0009898 maxillary shelf hypoplasia IAGP N RGD:5509061 20221006 MGI PMID:35212626 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0010745 abnormal pre-Botzinger complex morphology IAGP N RGD:5509061 20141003 MGI PMID:23103168 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0010746 abnormal pre-Botzinger complex physiology IAGP N RGD:5509061 20141003 MGI PMID:23103168 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23103168 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23103168 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221006 MGI PMID:35212626 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0012174 flat head IAGP N RGD:5509061 20221006 MGI PMID:35212626 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0013475 delayed reproductive senescence IAGP N RGD:5509061 20220616 MGI PMID:23967333 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0014106 delayed chondrocyte differentiation IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160929 MGI PMID:25587042 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:35212626 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:35212626 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0021216 abnormal palatal mesenchymal cell differentiation IAGP N RGD:5509061 20230302 MGI PMID:35212626 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0030224 abnormal soft palate muscle morphology IAGP N RGD:5509061 20221006 MGI PMID:35212626 1316935 Kdm6b KDM1 lysine (K)-specific demethylase 6B gene MP:0031425 enhanced male fertility IAGP N RGD:5509061 20220714 MGI PMID:23967333 1316941 Chaf1b chromatin assembly factor 1, subunit B gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 1316941 Chaf1b chromatin assembly factor 1, subunit B gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20190103 MGI PMID:30423293 1316941 Chaf1b chromatin assembly factor 1, subunit B gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20190103 MGI PMID:30423293 1316941 Chaf1b chromatin assembly factor 1, subunit B gene MP:0002083 premature death IAGP N RGD:5509061 20190103 MGI PMID:30423293 1316941 Chaf1b chromatin assembly factor 1, subunit B gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20190103 MGI PMID:30423293 1316941 Chaf1b chromatin assembly factor 1, subunit B gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20190103 MGI PMID:30423293 1316941 Chaf1b chromatin assembly factor 1, subunit B gene MP:0005152 pancytopenia IAGP N RGD:5509061 20190103 MGI PMID:30423293 1316941 Chaf1b chromatin assembly factor 1, subunit B gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20240523 MGI 1316941 Chaf1b chromatin assembly factor 1, subunit B gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20190103 MGI PMID:30423293 1316941 Chaf1b chromatin assembly factor 1, subunit B gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1316941 Chaf1b chromatin assembly factor 1, subunit B gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20190103 MGI PMID:30423293 1316941 Chaf1b chromatin assembly factor 1, subunit B gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20190103 MGI PMID:30423293 1316941 Chaf1b chromatin assembly factor 1, subunit B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316941 Chaf1b chromatin assembly factor 1, subunit B gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20190103 MGI PMID:30423293 1316941 Chaf1b chromatin assembly factor 1, subunit B gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 1316945 Zfp131 zinc finger protein 131 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20211021 MGI PMID:26136427 1316945 Zfp131 zinc finger protein 131 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20211021 MGI PMID:26136427 1316945 Zfp131 zinc finger protein 131 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20211021 MGI PMID:26136427 1316945 Zfp131 zinc finger protein 131 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20211021 MGI PMID:26136427 1316945 Zfp131 zinc finger protein 131 gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20211021 MGI PMID:26136427 1316945 Zfp131 zinc finger protein 131 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20211021 MGI PMID:26136427 1316945 Zfp131 zinc finger protein 131 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20211021 MGI PMID:26136427 1316945 Zfp131 zinc finger protein 131 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20211021 MGI PMID:26136427 1316945 Zfp131 zinc finger protein 131 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20211021 MGI PMID:26136427 1316945 Zfp131 zinc finger protein 131 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20211021 MGI PMID:26136427 1316945 Zfp131 zinc finger protein 131 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20211021 MGI PMID:26136427 1316945 Zfp131 zinc finger protein 131 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20211021 MGI PMID:26136427 1316945 Zfp131 zinc finger protein 131 gene MP:0010132 decreased DN2 thymocyte number IAGP N RGD:5509061 20211021 MGI PMID:26136427 1316945 Zfp131 zinc finger protein 131 gene MP:0010134 decreased DN3 thymocyte number IAGP N RGD:5509061 20211021 MGI PMID:26136427 1316945 Zfp131 zinc finger protein 131 gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20211021 MGI PMID:26136427 1316948 Arsj arylsulfatase J gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210826 MGI 1316948 Arsj arylsulfatase J gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1316948 Arsj arylsulfatase J gene MP:0002626 increased heart rate IEA N RGD:5509061 20210826 MGI 1316948 Arsj arylsulfatase J gene MP:0002833 increased heart weight IEA N RGD:5509061 20220519 MGI 1316948 Arsj arylsulfatase J gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210826 MGI 1316948 Arsj arylsulfatase J gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1316948 Arsj arylsulfatase J gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210826 MGI 1316948 Arsj arylsulfatase J gene MP:0010507 shortened RR interval IEA N RGD:5509061 20220519 MGI 1316958 Lpin1 lipin 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0000424 retarded hair growth IAGP N RGD:5509061 20141003 MGI PMID:2722772 1316958 Lpin1 lipin 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:11138012 1316958 Lpin1 lipin 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11138012 1316958 Lpin1 lipin 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:18559480 1316958 Lpin1 lipin 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:18559480 1316958 Lpin1 lipin 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0000958 peripheral nervous system degeneration IAGP N RGD:5509061 20141003 MGI PMID:11138012 1316958 Lpin1 lipin 1 gene MP:0001105 abnormal PNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18559480 1316958 Lpin1 lipin 1 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191226 MGI PMID:24634820 1316958 Lpin1 lipin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20191226 MGI PMID:24634820 1316958 Lpin1 lipin 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11138012 1316958 Lpin1 lipin 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18559480 1316958 Lpin1 lipin 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:18559480 1316958 Lpin1 lipin 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:2722772 1316958 Lpin1 lipin 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:2722772 1316958 Lpin1 lipin 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160128 MGI PMID:22908270 1316958 Lpin1 lipin 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11138012 1316958 Lpin1 lipin 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17130489 1316958 Lpin1 lipin 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18559480 1316958 Lpin1 lipin 1 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:11138012 1316958 Lpin1 lipin 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18559480 1316958 Lpin1 lipin 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20160128 MGI PMID:22908270 1316958 Lpin1 lipin 1 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:17130489 1316958 Lpin1 lipin 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18669885 1316958 Lpin1 lipin 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160128 MGI PMID:22908270 1316958 Lpin1 lipin 1 gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:17130489 1316958 Lpin1 lipin 1 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:17130489 1316958 Lpin1 lipin 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17130489 1316958 Lpin1 lipin 1 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20191226 MGI PMID:24634820 1316958 Lpin1 lipin 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:17130489 1316958 Lpin1 lipin 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11138012 1316958 Lpin1 lipin 1 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20191226 MGI PMID:24634820 1316958 Lpin1 lipin 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:18559480 1316958 Lpin1 lipin 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0005440 increased glycogen level IAGP N RGD:5509061 20141003 MGI PMID:17130489 1316958 Lpin1 lipin 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17130489 1316958 Lpin1 lipin 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20191226 MGI PMID:24634820 1316958 Lpin1 lipin 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11138012 1316958 Lpin1 lipin 1 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21397848 1316958 Lpin1 lipin 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:2722772 1316958 Lpin1 lipin 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:18559480 1316958 Lpin1 lipin 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0008976 delayed female fertility IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11138012 1316958 Lpin1 lipin 1 gene MP:0009122 decreased white fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:11138012 1316958 Lpin1 lipin 1 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:11138012 1316958 Lpin1 lipin 1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18669885 1316958 Lpin1 lipin 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:24634820 1316958 Lpin1 lipin 1 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0010052 increased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2722772 1316958 Lpin1 lipin 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160128 MGI PMID:22908270 1316958 Lpin1 lipin 1 gene MP:0011579 decreased lipoprotein lipase activity IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0011582 decreased triglyceride lipase activity IAGP N RGD:5509061 20141003 MGI PMID:2050689 1316958 Lpin1 lipin 1 gene MP:0011591 decreased hormone-sensitive lipase activity IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20160407 MGI PMID:11138012 1316958 Lpin1 lipin 1 gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:11138012 1316958 Lpin1 lipin 1 gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:10884287 1316958 Lpin1 lipin 1 gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:11138012 1316958 Lpin1 lipin 1 gene MP:0030863 decreased joint mobility IAGP N RGD:5509061 20181101 MGI PMID:19793967 1316958 Lpin1 lipin 1 gene MP:0031203 forelimb paresis IAGP N RGD:5509061 20210218 MGI PMID:19793967 1316960 Sytl2 synaptotagmin-like 2 gene MP:0000505 decreased digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:16716193 1316960 Sytl2 synaptotagmin-like 2 gene MP:0004137 abnormal gastric surface mucous cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16716193 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:20080492 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:21746835 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:20080492 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:21746835 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:20080492 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:21746835 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20080492 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21746835 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20080492 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:21746835 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21746835 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20080492 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21746835 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0002236 abnormal internal nares morphology IAGP N RGD:5509061 20141003 MGI PMID:21746835 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20080492 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21746835 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20080492 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21746835 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:20080492 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:21746835 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20080492 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:20080492 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:21746835 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20141003 MGI PMID:20080492 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20141003 MGI PMID:21746835 1316961 Dpcd deleted in primary ciliary dyskinesia gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:20080492 1316963 Wdr6 WD repeat domain 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1316963 Wdr6 WD repeat domain 6 gene MP:0001513 limb grasping IEA N RGD:5509061 20220811 MGI 1316963 Wdr6 WD repeat domain 6 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20220811 MGI 1316963 Wdr6 WD repeat domain 6 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20231207 MGI 1316963 Wdr6 WD repeat domain 6 gene MP:0010507 shortened RR interval IEA N RGD:5509061 20240523 MGI 1316963 Wdr6 WD repeat domain 6 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20231207 MGI 1316967 Cblc Casitas B-lineage lymphoma c gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14560016 1316968 Psg16 pregnancy specific beta-1-glycoprotein 16 gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 1316970 Ap1m1 adaptor-related protein complex AP-1, mu subunit 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10811610 1316970 Ap1m1 adaptor-related protein complex AP-1, mu subunit 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10811610 1316972 Rit1 Ras-like without CAAX 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0000445 short snout IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0001255 decreased body height IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1316972 Rit1 Ras-like without CAAX 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0001577 anemia IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0002083 premature death IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1316972 Rit1 Ras-like without CAAX 1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1316972 Rit1 Ras-like without CAAX 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1316972 Rit1 Ras-like without CAAX 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1316972 Rit1 Ras-like without CAAX 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:21737674 1316972 Rit1 Ras-like without CAAX 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1316972 Rit1 Ras-like without CAAX 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316972 Rit1 Ras-like without CAAX 1 gene MP:0030245 round head IAGP N RGD:5509061 20190905 MGI PMID:30898653 1316975 Dppa1 developmental pluripotency associated 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20141003 MGI 1316975 Dppa1 developmental pluripotency associated 1 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20181227 MGI 1316975 Dppa1 developmental pluripotency associated 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20170105 MGI 1316975 Dppa1 developmental pluripotency associated 1 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20181227 MGI 1316975 Dppa1 developmental pluripotency associated 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1316975 Dppa1 developmental pluripotency associated 1 gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20210128 MGI 1316975 Dppa1 developmental pluripotency associated 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316975 Dppa1 developmental pluripotency associated 1 gene MP:0011939 increased food intake IEA N RGD:5509061 20211021 MGI 1316975 Dppa1 developmental pluripotency associated 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1316982 Tbc1d7 TBC1 domain family, member 7 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20220630 MGI PMID:35584673 1316982 Tbc1d7 TBC1 domain family, member 7 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20220630 MGI PMID:35584673 1316982 Tbc1d7 TBC1 domain family, member 7 gene MP:0001407 short stride length IAGP N RGD:5509061 20220630 MGI PMID:35584673 1316982 Tbc1d7 TBC1 domain family, member 7 gene MP:0001513 limb grasping IAGP N RGD:5509061 20220630 MGI PMID:35584673 1316982 Tbc1d7 TBC1 domain family, member 7 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20220630 MGI PMID:35584673 1316982 Tbc1d7 TBC1 domain family, member 7 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20220630 MGI PMID:35584673 1316982 Tbc1d7 TBC1 domain family, member 7 gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20220630 MGI PMID:35584673 1316982 Tbc1d7 TBC1 domain family, member 7 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20220630 MGI PMID:35584673 1316982 Tbc1d7 TBC1 domain family, member 7 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20220630 MGI PMID:35584673 1316982 Tbc1d7 TBC1 domain family, member 7 gene MP:0005238 increased brain size IAGP N RGD:5509061 20220630 MGI PMID:35584673 1316982 Tbc1d7 TBC1 domain family, member 7 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20220630 MGI PMID:35584673 1316982 Tbc1d7 TBC1 domain family, member 7 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20220630 MGI PMID:35584673 1316982 Tbc1d7 TBC1 domain family, member 7 gene MP:0031392 hypoactivity IAGP N RGD:5509061 20220630 MGI PMID:35584673 1316984 Ankrd9 ankyrin repeat domain 9 gene MP:0001257 increased body length IEA N RGD:5509061 20201022 MGI 1316984 Ankrd9 ankyrin repeat domain 9 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1316984 Ankrd9 ankyrin repeat domain 9 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1316984 Ankrd9 ankyrin repeat domain 9 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150430 MGI 1316984 Ankrd9 ankyrin repeat domain 9 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20150430 MGI 1316984 Ankrd9 ankyrin repeat domain 9 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20150430 MGI 1316986 Peg12 paternally expressed 12 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15681612 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20160818 MGI PMID:25708872 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0000914 exencephaly IAGP N RGD:5509061 20160818 MGI PMID:25708872 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20160818 MGI PMID:25708872 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0000929 open neural tube IAGP N RGD:5509061 20160818 MGI PMID:25708872 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20160818 MGI PMID:25708872 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20160818 MGI PMID:25708872 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160818 MGI PMID:25708872 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20160818 MGI PMID:25708872 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:20858271 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:20858271 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20160818 MGI PMID:25708872 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160818 MGI PMID:25708872 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:20858271 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20210128 MGI 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20160818 MGI PMID:25708872 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0008830 abnormal nucleolus morphology IAGP N RGD:5509061 20141003 MGI PMID:20858271 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:20858271 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20858271 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160818 MGI PMID:25708872 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1316987 Emg1 EMG1 N1-specific pseudouridine methyltransferase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1316993 Myoz2 myozenin 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:22987565 1316993 Myoz2 myozenin 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:22987565 1316993 Myoz2 myozenin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:22987565 1316993 Myoz2 myozenin 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:22987565 1316993 Myoz2 myozenin 2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:22987565 1316993 Myoz2 myozenin 2 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:22987565 1316993 Myoz2 myozenin 2 gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22987565 1316993 Myoz2 myozenin 2 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:15543153 1316993 Myoz2 myozenin 2 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:22987565 1316996 Med23 mediator complex subunit 23 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0000128 growth retardation of molars IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:19417216 1316996 Med23 mediator complex subunit 23 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20210128 MGI PMID:21305688 1316996 Med23 mediator complex subunit 23 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1316996 Med23 mediator complex subunit 23 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20210128 MGI PMID:21305688 1316996 Med23 mediator complex subunit 23 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20210128 MGI PMID:21305688 1316996 Med23 mediator complex subunit 23 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1316996 Med23 mediator complex subunit 23 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1316996 Med23 mediator complex subunit 23 gene MP:0002639 micrognathia IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1316996 Med23 mediator complex subunit 23 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:19417216 1316996 Med23 mediator complex subunit 23 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20210128 MGI PMID:21305688 1316996 Med23 mediator complex subunit 23 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210520 MGI 1316996 Med23 mediator complex subunit 23 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19417216 1316996 Med23 mediator complex subunit 23 gene MP:0004424 temporal bone hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0004592 small mandible IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1316996 Med23 mediator complex subunit 23 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1316996 Med23 mediator complex subunit 23 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22972934 1316996 Med23 mediator complex subunit 23 gene MP:0005359 growth retardation of incisors IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20210128 MGI PMID:21305688 1316996 Med23 mediator complex subunit 23 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210520 MGI 1316996 Med23 mediator complex subunit 23 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1316996 Med23 mediator complex subunit 23 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 1316996 Med23 mediator complex subunit 23 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19417216 1316996 Med23 mediator complex subunit 23 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20210128 MGI PMID:21305688 1316996 Med23 mediator complex subunit 23 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1316996 Med23 mediator complex subunit 23 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1316996 Med23 mediator complex subunit 23 gene MP:0012756 impaired cranial neural crest cell differentiation IAGP N RGD:5509061 20210128 MGI PMID:21305688 1316996 Med23 mediator complex subunit 23 gene MP:0013268 second pharyngeal arch hypoplasia IAGP N RGD:5509061 20210128 MGI PMID:21305688 1316996 Med23 mediator complex subunit 23 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0030080 small lower incisors IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0030170 absent mandibular symphysis IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0030249 small frontonasal prominence IAGP N RGD:5509061 20210128 MGI PMID:21305688 1316996 Med23 mediator complex subunit 23 gene MP:0030259 mandibular condyloid process hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0030374 Meckel's cartilage hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0030467 abnormal cranial cartilage development IAGP N RGD:5509061 20221020 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0031444 glossoptosis IAGP N RGD:5509061 20221027 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:33155500 1316996 Med23 mediator complex subunit 23 gene MP:0031450 nasal cartilage hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:33155500 1316998 Zup1 zinc finger containing ubiquitin peptidase 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20240829 MGI PMID:38460305 1316998 Zup1 zinc finger containing ubiquitin peptidase 1 gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20240829 MGI PMID:38460305 1316998 Zup1 zinc finger containing ubiquitin peptidase 1 gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20240829 MGI PMID:38460305 1316999 Mcur1 mitochondrial calcium uniporter regulator 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20171116 MGI PMID:27184846 1316999 Mcur1 mitochondrial calcium uniporter regulator 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20171116 MGI PMID:27184846 1316999 Mcur1 mitochondrial calcium uniporter regulator 1 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20171116 MGI PMID:27184846 1316999 Mcur1 mitochondrial calcium uniporter regulator 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20171116 MGI PMID:27184846 1316999 Mcur1 mitochondrial calcium uniporter regulator 1 gene MP:0011134 decreased lung endothelial cell migration IAGP N RGD:5509061 20171116 MGI PMID:27184846 1316999 Mcur1 mitochondrial calcium uniporter regulator 1 gene MP:0011140 decreased lung endothelial cell proliferation IAGP N RGD:5509061 20171116 MGI PMID:27184846 1317001 Slmap sarcolemma associated protein gene MP:0000111 cleft palate IEA N RGD:5509061 20111116 MGI 1317001 Slmap sarcolemma associated protein gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20240808 MGI PMID:38474134 1317001 Slmap sarcolemma associated protein gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20240808 MGI PMID:38474134 1317001 Slmap sarcolemma associated protein gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1317001 Slmap sarcolemma associated protein gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20201022 MGI 1317001 Slmap sarcolemma associated protein gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20201022 MGI 1317001 Slmap sarcolemma associated protein gene MP:0002188 small heart IAGP N RGD:5509061 20240808 MGI PMID:38474134 1317001 Slmap sarcolemma associated protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317001 Slmap sarcolemma associated protein gene MP:0011495 abnormal head shape IEA N RGD:5509061 20201022 MGI 1317001 Slmap sarcolemma associated protein gene MP:0011496 abnormal head size IEA N RGD:5509061 20201022 MGI 1317001 Slmap sarcolemma associated protein gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20240808 MGI PMID:38474134 1317001 Slmap sarcolemma associated protein gene MP:0031536 decreased heart atrium wall thickness IAGP N RGD:5509061 20240808 MGI PMID:38474134 1317001 Slmap sarcolemma associated protein gene MP:0031608 decreased fetal cardiomyocyte size IAGP N RGD:5509061 20240808 MGI PMID:38474134 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12421714 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:12372301 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:12372301 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:12421714 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:12372258 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12372258 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:15315763 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:12421714 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:12421714 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:12372258 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15755804 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:12372301 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12372301 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12372301 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12421714 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12372301 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15755804 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:12372258 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:16611729 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12372258 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12372301 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12421714 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0002243 abnormal vomeronasal organ morphology IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0002251 abnormal nasopharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0002659 pituitary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:12372301 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12372258 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20141003 MGI PMID:12421714 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:12372258 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:12421714 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0004419 absent parietal bone IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0004419 absent parietal bone IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0004440 absent occipital bone IAGP N RGD:5509061 20171102 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0004790 absent upper incisors IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:12372301 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:12421714 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:12421714 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0005224 abnormal left-right axis symmetry of the somites IAGP N RGD:5509061 20141003 MGI PMID:12421714 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0005315 absent pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12372301 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:12421714 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20171019 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0006290 proboscis IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0006306 abnormal nasal pit morphology IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:12372301 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0008385 absent basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:16611729 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0010335 fused first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:12372301 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16611729 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12372258 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15576405 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12372258 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12372301 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12421714 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20141003 MGI PMID:12372258 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0012258 philtrum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0013595 absent vomeronasal organ IAGP N RGD:5509061 20150319 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0014106 delayed chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:15269168 1317003 Disp1 dispatched RND transporter family member 1 gene MP:0030314 absent primary palate IAGP N RGD:5509061 20171109 MGI PMID:15269168 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20150521 MGI PMID:24766809 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0000160 kyphosis IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0000433 microcephaly IAGP N RGD:5509061 20150521 MGI PMID:24766809 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0000745 tremors IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0000774 decreased brain size IAGP N RGD:5509061 20150521 MGI PMID:24766809 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20150521 MGI PMID:24766809 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0001080 defasiculated phrenic nerve IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0001406 abnormal gait IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20150521 MGI PMID:24766809 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20150521 MGI PMID:24766809 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20150521 MGI PMID:24766809 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20150521 MGI PMID:24766809 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0009959 abnormal cerebellar hemisphere morphology IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0009980 abnormal cerebellum dentate nucleus morphology IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20141003 MGI PMID:23474986 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20211021 MGI PMID:34548404 1317008 Clp1 CLP1, cleavage and polyadenylation factor I subunit gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:34548404 1317011 Ctsg cathepsin G gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12750176 1317011 Ctsg cathepsin G gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12750176 1317011 Ctsg cathepsin G gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:12750176 1317011 Ctsg cathepsin G gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:20647568 1317011 Ctsg cathepsin G gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12750176 1317011 Ctsg cathepsin G gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20647568 1317011 Ctsg cathepsin G gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12750176 1317011 Ctsg cathepsin G gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12750176 1317011 Ctsg cathepsin G gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14636558 1317011 Ctsg cathepsin G gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:12750176 1317011 Ctsg cathepsin G gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:14636558 1317011 Ctsg cathepsin G gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20647568 1317011 Ctsg cathepsin G gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10590073 1317011 Ctsg cathepsin G gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12750176 1317011 Ctsg cathepsin G gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20647568 1317011 Ctsg cathepsin G gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12750176 1317011 Ctsg cathepsin G gene MP:0004049 increased acute promyelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:20647568 1317011 Ctsg cathepsin G gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:20647568 1317011 Ctsg cathepsin G gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:10714686 1317011 Ctsg cathepsin G gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20647568 1317011 Ctsg cathepsin G gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:10714686 1317011 Ctsg cathepsin G gene MP:0009787 increased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10714686 1317011 Ctsg cathepsin G gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10714686 1317012 Ift46 intraflagellar transport 46 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20160421 MGI PMID:25722189 1317012 Ift46 intraflagellar transport 46 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20160421 MGI PMID:25722189 1317012 Ift46 intraflagellar transport 46 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20160421 MGI PMID:25722189 1317012 Ift46 intraflagellar transport 46 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20160421 MGI PMID:25722189 1317012 Ift46 intraflagellar transport 46 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20160421 MGI PMID:25722189 1317012 Ift46 intraflagellar transport 46 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160421 MGI PMID:25722189 1317012 Ift46 intraflagellar transport 46 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20160421 MGI PMID:25722189 1317012 Ift46 intraflagellar transport 46 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20160421 MGI PMID:25722189 1317012 Ift46 intraflagellar transport 46 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160421 MGI PMID:25722189 1317012 Ift46 intraflagellar transport 46 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20160421 MGI PMID:25722189 1317012 Ift46 intraflagellar transport 46 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20160421 MGI PMID:25722189 1317012 Ift46 intraflagellar transport 46 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20160421 MGI PMID:25722189 1317012 Ift46 intraflagellar transport 46 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160421 MGI PMID:25722189 1317012 Ift46 intraflagellar transport 46 gene MP:0012093 absent nodal flow IAGP N RGD:5509061 20160421 MGI PMID:25722189 1317012 Ift46 intraflagellar transport 46 gene MP:0012270 cardiac edema IAGP N RGD:5509061 20160421 MGI PMID:25722189 1317016 Extl2 exostosin-like glycosyltransferase 2 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23395820 1317018 Cavin1 caveolae associated 1 gene MP:0000741 impaired contractility of urinary bladder detrusor smooth muscle IAGP N RGD:5509061 20150219 MGI PMID:22643325 1317018 Cavin1 caveolae associated 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20150312 MGI PMID:24303100 1317018 Cavin1 caveolae associated 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18840361 1317018 Cavin1 caveolae associated 1 gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:18840361 1317018 Cavin1 caveolae associated 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18840361 1317018 Cavin1 caveolae associated 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18840361 1317018 Cavin1 caveolae associated 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18840361 1317018 Cavin1 caveolae associated 1 gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20150312 MGI PMID:24303100 1317018 Cavin1 caveolae associated 1 gene MP:0003913 increased heart right ventricle weight IAGP N RGD:5509061 20150312 MGI PMID:24303100 1317018 Cavin1 caveolae associated 1 gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:18840361 1317018 Cavin1 caveolae associated 1 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:18840361 1317018 Cavin1 caveolae associated 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23652019 1317018 Cavin1 caveolae associated 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20150312 MGI PMID:24303100 1317018 Cavin1 caveolae associated 1 gene MP:0004150 absent caveolae IAGP N RGD:5509061 20141003 MGI PMID:18840361 1317018 Cavin1 caveolae associated 1 gene MP:0004150 absent caveolae IAGP N RGD:5509061 20141003 MGI PMID:23652019 1317018 Cavin1 caveolae associated 1 gene MP:0004150 absent caveolae IAGP N RGD:5509061 20150312 MGI PMID:22643325 1317018 Cavin1 caveolae associated 1 gene MP:0004150 absent caveolae IAGP N RGD:5509061 20150312 MGI PMID:24303100 1317018 Cavin1 caveolae associated 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18840361 1317018 Cavin1 caveolae associated 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:18840361 1317018 Cavin1 caveolae associated 1 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:18840361 1317018 Cavin1 caveolae associated 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18840361 1317018 Cavin1 caveolae associated 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23652019 1317018 Cavin1 caveolae associated 1 gene MP:0010758 increased right ventricle systolic pressure IAGP N RGD:5509061 20150312 MGI PMID:24303100 1317018 Cavin1 caveolae associated 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20150219 MGI PMID:22643325 1317018 Cavin1 caveolae associated 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20150219 MGI PMID:22643325 1317018 Cavin1 caveolae associated 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23652019 1317018 Cavin1 caveolae associated 1 gene MP:0011774 abnormal urinary bladder detrusor smooth muscle morphology IAGP N RGD:5509061 20150219 MGI PMID:22643325 1317018 Cavin1 caveolae associated 1 gene MP:0011799 increased urinary bladder weight IAGP N RGD:5509061 20150219 MGI PMID:22643325 1317018 Cavin1 caveolae associated 1 gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20160421 MGI PMID:18840361 1317021 Isy1 ISY1 splicing factor homolog gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1317021 Isy1 ISY1 splicing factor homolog gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20240926 MGI 1317021 Isy1 ISY1 splicing factor homolog gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240926 MGI 1317021 Isy1 ISY1 splicing factor homolog gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20240926 MGI 1317021 Isy1 ISY1 splicing factor homolog gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1317021 Isy1 ISY1 splicing factor homolog gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20240926 MGI 1317021 Isy1 ISY1 splicing factor homolog gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16554754 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16554754 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:16554754 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9442388 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9710223 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9846484 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9442388 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9710223 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:9710223 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9846484 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12787506 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12787506 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16554754 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12787506 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9846484 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:9442388 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:9710223 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:9710223 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9846484 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:9846484 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17579027 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:9442388 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:9846484 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:9710223 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:9710223 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17579027 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12150890 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9442388 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9710223 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:9710223 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21464221 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9710223 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14573689 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:14573689 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:16554754 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:9442388 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16554754 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:9710223 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:16554754 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16554754 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9442388 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9442388 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9846484 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9442388 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9846484 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9846484 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:9846484 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14573689 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:14573689 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:14573689 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17579027 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9442388 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:14573689 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:12150890 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:14573689 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:9442388 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:12150890 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:21464221 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20240509 MGI PMID:38457343 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:14573689 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:12150890 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:14573689 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:12787506 1317024 Nfatc2 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16554754 1317030 Kifc3 kinesin family member C3 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20220811 MGI 1317033 Kif20a kinesin family member 20A gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1317033 Kif20a kinesin family member 20A gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1317033 Kif20a kinesin family member 20A gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160421 MGI 1317033 Kif20a kinesin family member 20A gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20240523 MGI 1317033 Kif20a kinesin family member 20A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20181227 MGI 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0000603 pale liver IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0003914 decreased heart right ventricle weight IAGP N RGD:5509061 20210429 MGI PMID:30923760 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0009137 decreased brown fat lipid droplet number IAGP N RGD:5509061 20160218 MGI PMID:24519944 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20221215 MGI 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210429 MGI PMID:30923760 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0010580 decreased heart left ventricle size IAGP N RGD:5509061 20210429 MGI PMID:30923760 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20210429 MGI PMID:30923760 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317035 Fitm2 fat storage-inducing transmembrane protein 2 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20210520 MGI 1317038 Ptpdc1 protein tyrosine phosphatase domain containing 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1317038 Ptpdc1 protein tyrosine phosphatase domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200102 MGI PMID:26306008 1317038 Ptpdc1 protein tyrosine phosphatase domain containing 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20190502 MGI 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20190502 MGI 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20190502 MGI 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220714 MGI PMID:31664153 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20220714 MGI PMID:31664153 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220714 MGI PMID:31664153 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0002833 increased heart weight IEA N RGD:5509061 20221215 MGI 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20231207 MGI 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220714 MGI PMID:31664153 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220714 MGI PMID:31664153 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0009709 hydrometra IEA N RGD:5509061 20190502 MGI 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220714 MGI PMID:31664153 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20221103 MGI 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0014190 abnormal epididymis physiology IAGP N RGD:5509061 20220714 MGI PMID:31664153 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:31664153 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220714 MGI PMID:31664153 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0031301 chronic liver inflammation IAGP N RGD:5509061 20211028 MGI PMID:24332041 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0031425 enhanced male fertility IAGP N RGD:5509061 20220714 MGI PMID:31664153 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0031426 increased sperm motility IAGP N RGD:5509061 20220714 MGI PMID:31664153 1317044 Ncoa5 nuclear receptor coactivator 5 gene MP:0031427 increased sperm progressive motility IAGP N RGD:5509061 20220714 MGI PMID:31664153 1317047 Riox1 ribosomal oxygenase 1 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0001257 increased body length IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0009673 increased birth weight IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20160505 MGI PMID:25736226 1317047 Riox1 ribosomal oxygenase 1 gene MP:0030278 thick neurocranium IAGP N RGD:5509061 20171102 MGI PMID:25736226 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:14517283 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19464366 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:14517283 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14517283 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19464366 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:19464366 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:19464366 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:19464366 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:14517283 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:14517283 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:14517283 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:19464366 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:14517283 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:14517283 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:19464366 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:14517283 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19464366 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:19464366 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0004266 pale placenta IAGP N RGD:5509061 20141003 MGI PMID:19464366 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:14517283 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:14517283 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19464366 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:14517283 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14517283 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19464366 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:14517283 1317049 Pak4 p21 (RAC1) activated kinase 4 gene MP:0021101 abnormal ventral interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:14517283 1317051 Commd9 COMM domain containing 9 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1317051 Commd9 COMM domain containing 9 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1317051 Commd9 COMM domain containing 9 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317051 Commd9 COMM domain containing 9 gene MP:0001785 edema IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317051 Commd9 COMM domain containing 9 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317051 Commd9 COMM domain containing 9 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317051 Commd9 COMM domain containing 9 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317051 Commd9 COMM domain containing 9 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317051 Commd9 COMM domain containing 9 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317051 Commd9 COMM domain containing 9 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317051 Commd9 COMM domain containing 9 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210128 MGI 1317051 Commd9 COMM domain containing 9 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1317051 Commd9 COMM domain containing 9 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317051 Commd9 COMM domain containing 9 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317051 Commd9 COMM domain containing 9 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1317051 Commd9 COMM domain containing 9 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317051 Commd9 COMM domain containing 9 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1317051 Commd9 COMM domain containing 9 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160421 MGI 1317051 Commd9 COMM domain containing 9 gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317051 Commd9 COMM domain containing 9 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1317051 Commd9 COMM domain containing 9 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20160421 MGI 1317051 Commd9 COMM domain containing 9 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317051 Commd9 COMM domain containing 9 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317051 Commd9 COMM domain containing 9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317051 Commd9 COMM domain containing 9 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317051 Commd9 COMM domain containing 9 gene MP:0014012 abnormal cranial blood vasculature morphology IAGP N RGD:5509061 20161013 MGI PMID:26553930 1317053 Ext2 exostosin glycosyltransferase 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:16236767 1317053 Ext2 exostosin glycosyltransferase 2 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:16236767 1317053 Ext2 exostosin glycosyltransferase 2 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:16236767 1317053 Ext2 exostosin glycosyltransferase 2 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:16236767 1317053 Ext2 exostosin glycosyltransferase 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:16236767 1317053 Ext2 exostosin glycosyltransferase 2 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:16236767 1317053 Ext2 exostosin glycosyltransferase 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16236767 1317053 Ext2 exostosin glycosyltransferase 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16236767 1317053 Ext2 exostosin glycosyltransferase 2 gene MP:0009877 exostosis IAGP N RGD:5509061 20141003 MGI PMID:16236767 1317053 Ext2 exostosin glycosyltransferase 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16236767 1317053 Ext2 exostosin glycosyltransferase 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17116694 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:14517553 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000041 absent endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000041 absent endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000041 absent endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000044 absent organ of Corti IAGP N RGD:5509061 20141003 MGI PMID:10072433 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:12783782 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:14628042 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:12070080 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0001072 abnormal vestibulocochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0001086 absent petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10072433 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:14517553 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:10072433 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:14517553 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10072433 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:10072433 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22340499 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0002659 pituitary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14628042 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:14517553 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003110 absent malleus processus brevis IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003142 anotia IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003147 absent cochlea IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003147 absent cochlea IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:10072433 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:10072433 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003164 decreased posterior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003164 decreased posterior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003166 decreased superior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003166 decreased superior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10072433 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12783782 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14628042 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003499 thyroid gland hypoplasia IAGP N RGD:5509061 20150122 MGI PMID:12070080 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:10072433 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:12783782 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:14628042 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003740 fusion of middle ear ossicles IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004248 abnormal epaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:14628042 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004299 absent vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004314 absent inner ear vestibule IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004315 absent vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004317 small vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004328 decreased vestibular hair cell number IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:22340499 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:22340499 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004427 abnormal vestibular labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004506 abnormal pubis morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004507 abnormal ischium morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004539 absent maxilla IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004922 abnormal common crus morphology IAGP N RGD:5509061 20141003 MGI PMID:10072433 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12783782 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0005247 abnormal extraocular muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:14628042 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:10072433 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006018 abnormal tympanic membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:12783782 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006033 abnormal external auditory canal morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006284 absent hypaxial muscle IAGP N RGD:5509061 20141003 MGI PMID:14628042 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006285 absent inner ear IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0006285 absent inner ear IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0008063 increased otic epithelial cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0008063 increased otic epithelial cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0008064 decreased otic epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0008065 short endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0008065 short endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20141003 MGI PMID:18678597 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0009707 absent external auditory canal IAGP N RGD:5509061 20170921 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16990542 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0009895 decreased palatine bone horizontal plate size IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0009897 decreased maxillary shelf size IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0010466 vascular ring IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10072433 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:10072433 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:14517553 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0013163 absent thyroid gland isthmus IAGP N RGD:5509061 20150122 MGI PMID:12070080 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0013222 abnormal first pharyngeal pouch morphology IAGP N RGD:5509061 20150101 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0013290 persistent ultimobranchial bodies IAGP N RGD:5509061 20150129 MGI PMID:12070080 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0030097 preauricular pit IAGP N RGD:5509061 20170928 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0030155 absent tympanic cavity IAGP N RGD:5509061 20171005 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0030161 absent auditory bulla IAGP N RGD:5509061 20171005 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0030204 large nasal septum IAGP N RGD:5509061 20171012 MGI PMID:10471511 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0030421 tongue muscle hypoplasia IAGP N RGD:5509061 20171214 MGI PMID:21364285 1317055 Eya1 EYA transcriptional coactivator and phosphatase 1 gene MP:0030426 facial muscle hypoplasia IAGP N RGD:5509061 20171214 MGI PMID:21364285 1317062 Rsph1 radial spoke head 1 homolog (Chlamydomonas) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18453535 1317062 Rsph1 radial spoke head 1 homolog (Chlamydomonas) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18453535 1317062 Rsph1 radial spoke head 1 homolog (Chlamydomonas) gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18453535 1317062 Rsph1 radial spoke head 1 homolog (Chlamydomonas) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18453535 1317062 Rsph1 radial spoke head 1 homolog (Chlamydomonas) gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:18453535 1317062 Rsph1 radial spoke head 1 homolog (Chlamydomonas) gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:18453535 1317062 Rsph1 radial spoke head 1 homolog (Chlamydomonas) gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220303 MGI PMID:18453535 1317062 Rsph1 radial spoke head 1 homolog (Chlamydomonas) gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220303 MGI PMID:18453535 1317062 Rsph1 radial spoke head 1 homolog (Chlamydomonas) gene MP:0009852 increased Sertoli cell phagocytosis IAGP N RGD:5509061 20220303 MGI PMID:18453535 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20180329 MGI PMID:28028151 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0001194 dermatitis IAGP N RGD:5509061 20240613 MGI PMID:31405606 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:19898472 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22461490 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0001806 decreased IgM level IEA N RGD:5509061 20141003 MGI 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0001830 decreased activated T cell number IEA N RGD:5509061 20141003 MGI 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0002144 abnormal B cell differentiation IEA N RGD:5509061 20190606 MGI 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0002145 abnormal T cell differentiation IEA N RGD:5509061 20190606 MGI 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22461490 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180329 MGI PMID:28028151 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:19898472 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19898472 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22461490 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190606 MGI 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22461490 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0008076 abnormal CD4-positive T cell differentiation IEA N RGD:5509061 20190606 MGI 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22461490 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20190606 MGI 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:19898472 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:19898472 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:22461490 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0008183 absent marginal zone B cells IEA N RGD:5509061 20141003 MGI 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0008200 decreased follicular dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22461490 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:19898472 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20180329 MGI PMID:28028151 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0010072 increased pruritus IAGP N RGD:5509061 20240613 MGI PMID:31405606 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190606 MGI 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190606 MGI 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20190606 MGI 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190606 MGI 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20190606 MGI 1317066 Dock8 dedicator of cytokinesis 8 gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20160915 MGI 1317069 Tbx6 T-box 6 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20200730 MGI PMID:31888956 1317069 Tbx6 T-box 6 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0000154 rib fusion IAGP N RGD:5509061 20200730 MGI PMID:30307510 1317069 Tbx6 T-box 6 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:9490412 1317069 Tbx6 T-box 6 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18575602 1317069 Tbx6 T-box 6 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20150205 MGI PMID:21331042 1317069 Tbx6 T-box 6 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15755804 1317069 Tbx6 T-box 6 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20150205 MGI PMID:21331042 1317069 Tbx6 T-box 6 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:9490412 1317069 Tbx6 T-box 6 gene MP:0003401 enlarged tail bud IAGP N RGD:5509061 20141003 MGI PMID:9490412 1317069 Tbx6 T-box 6 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0004131 abnormal motile primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:18575602 1317069 Tbx6 T-box 6 gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:18575602 1317069 Tbx6 T-box 6 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:18575602 1317069 Tbx6 T-box 6 gene MP:0004600 abnormal vertebral transverse process morphology IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0004602 abnormal vertebral articular process morphology IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20200730 MGI PMID:30307510 1317069 Tbx6 T-box 6 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20200730 MGI PMID:31888956 1317069 Tbx6 T-box 6 gene MP:0004612 fusion of vertebral bodies IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0004669 enlarged vertebral body IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0004670 small vertebral body IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20200730 MGI PMID:30307510 1317069 Tbx6 T-box 6 gene MP:0005226 abnormal vertebral arch development IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0005227 abnormal vertebral body development IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15755804 1317069 Tbx6 T-box 6 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9490412 1317069 Tbx6 T-box 6 gene MP:0008817 hematoma IAGP N RGD:5509061 20141003 MGI PMID:9490412 1317069 Tbx6 T-box 6 gene MP:0008933 abnormal motile primary cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:18575602 1317069 Tbx6 T-box 6 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:9490412 1317069 Tbx6 T-box 6 gene MP:0010662 abnormal intersomitic artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9490412 1317069 Tbx6 T-box 6 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200730 MGI PMID:30307510 1317069 Tbx6 T-box 6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9490412 1317069 Tbx6 T-box 6 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:4073528 1317069 Tbx6 T-box 6 gene MP:0011998 decreased embryonic cilium length IAGP N RGD:5509061 20141003 MGI PMID:18575602 1317071 Tnip2 TNFAIP3 interacting protein 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16633345 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19801521 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10523604 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19801521 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11160319 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:11160319 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11160319 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11160319 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19017968 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11160319 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:19017968 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:19801521 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:11160319 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11160319 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19801521 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19801521 1317073 Cd3g CD3 antigen, gamma polypeptide gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11160319 1317075 Anxa8 annexin A8 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:24769558 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:16127460 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:15494444 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15494444 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15494444 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15494444 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15494444 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:15494444 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16127460 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:15494444 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:16127460 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15494444 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16127460 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15494444 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0002697 abnormal eye size IEA N RGD:5509061 20160804 MGI 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:15494444 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16127460 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:15494444 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16127460 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:24210661 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:15494444 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0009716 abnormal subcommissural organ morphology IAGP N RGD:5509061 20141003 MGI PMID:15494444 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0010167 decreased response to stress-induced hyperthermia IAGP N RGD:5509061 20160922 MGI PMID:24652767 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16127460 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0012538 persistent hyaloid artery IAGP N RGD:5509061 20160922 MGI PMID:24652767 1317077 Socs7 suppressor of cytokine signaling 7 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20160922 MGI PMID:24652767 1317079 Celf1 CUGBP, Elav-like family member 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17130239 1317079 Celf1 CUGBP, Elav-like family member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17130239 1317079 Celf1 CUGBP, Elav-like family member 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1317079 Celf1 CUGBP, Elav-like family member 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17130239 1317079 Celf1 CUGBP, Elav-like family member 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17130239 1317079 Celf1 CUGBP, Elav-like family member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17130239 1317079 Celf1 CUGBP, Elav-like family member 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17130239 1317079 Celf1 CUGBP, Elav-like family member 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17130239 1317079 Celf1 CUGBP, Elav-like family member 1 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:17130239 1317079 Celf1 CUGBP, Elav-like family member 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17130239 1317079 Celf1 CUGBP, Elav-like family member 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17130239 1317079 Celf1 CUGBP, Elav-like family member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317083 Dsel dermatan sulfate epimerase-like gene MP:0000192 abnormal mineral level IAGP N RGD:5509061 20141003 MGI PMID:22496542 1317083 Dsel dermatan sulfate epimerase-like gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:22496542 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0000111 cleft palate IAGP N RGD:5509061 20200514 MGI PMID:31600785 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0000373 belly spot IEA N RGD:5509061 20111116 MGI 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20141120 MGI PMID:24753090 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:19922873 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141120 MGI PMID:24753090 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:19922873 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200514 MGI PMID:31600785 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18454205 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0002095 abnormal skin pigmentation IEA N RGD:5509061 20171109 MGI 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0002671 belted IAGP N RGD:5509061 20141003 MGI PMID:10614578 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0002671 belted IAGP N RGD:5509061 20141003 MGI PMID:12925592 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0002671 belted IAGP N RGD:5509061 20141003 MGI PMID:14138974 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0002671 belted IAGP N RGD:5509061 20141003 MGI PMID:18454205 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0002671 belted IAGP N RGD:5509061 20141003 MGI PMID:5713933 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:10614578 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:18454205 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0002938 white spotting IAGP N RGD:5509061 20200514 MGI PMID:31600785 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0002940 variable body spotting IEA N RGD:5509061 20190103 MGI 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:5713933 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14138974 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0005072 abnormal hair follicle melanin granule morphology IAGP N RGD:5509061 20141120 MGI PMID:24753090 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0009555 abnormal hair follicle melanin granule distribution IAGP N RGD:5509061 20141003 MGI PMID:14138974 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:18454205 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20141120 MGI PMID:24753090 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0009784 abnormal melanoblast migration IAGP N RGD:5509061 20141003 MGI PMID:14138974 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0009784 abnormal melanoblast migration IAGP N RGD:5509061 20141003 MGI PMID:18454205 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0009874 abnormal interdigital cell death IAGP N RGD:5509061 20141003 MGI PMID:19922873 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141120 MGI PMID:24753090 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0010770 preweaning lethality IAGP N RGD:5509061 20200514 MGI PMID:31600785 1317085 Adamts20 ADAM metallopeptidase with thrombospondin type 1 motif 20 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18454205 1317091 Zc3h13 zinc finger CCCH type containing 13 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1317091 Zc3h13 zinc finger CCCH type containing 13 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201231 MGI 1317091 Zc3h13 zinc finger CCCH type containing 13 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1317091 Zc3h13 zinc finger CCCH type containing 13 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1317091 Zc3h13 zinc finger CCCH type containing 13 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1317091 Zc3h13 zinc finger CCCH type containing 13 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1317091 Zc3h13 zinc finger CCCH type containing 13 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 1317091 Zc3h13 zinc finger CCCH type containing 13 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1317091 Zc3h13 zinc finger CCCH type containing 13 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1317091 Zc3h13 zinc finger CCCH type containing 13 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317091 Zc3h13 zinc finger CCCH type containing 13 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20210520 MGI 1317093 Nfe2l3 nuclear factor, erythroid derived 2, like 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15060151 1317093 Nfe2l3 nuclear factor, erythroid derived 2, like 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15060151 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0000745 tremors IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0001513 limb grasping IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0002083 premature death IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0005150 cachexia IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0010129 increased DN1 thymic pro-T cell number IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0012051 spasticity IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0013585 thymus cortex atrophy IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317095 Dnajc11 DnaJ heat shock protein family (Hsp40) member C11 gene MP:0013590 enlarged thymus medulla IAGP N RGD:5509061 20160225 MGI PMID:25111180 1317097 Recql4 RecQ protein-like 4 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:15703196 1317097 Recql4 RecQ protein-like 4 gene MP:0000128 growth retardation of molars IAGP N RGD:5509061 20141003 MGI PMID:12915449 1317097 Recql4 RecQ protein-like 4 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:12915449 1317097 Recql4 RecQ protein-like 4 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20230601 MGI 1317097 Recql4 RecQ protein-like 4 gene MP:0000413 polyphalangy IAGP N RGD:5509061 20141003 MGI PMID:15703196 1317097 Recql4 RecQ protein-like 4 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12915449 1317097 Recql4 RecQ protein-like 4 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:12915449 1317097 Recql4 RecQ protein-like 4 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12915449 1317097 Recql4 RecQ protein-like 4 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:12915449 1317097 Recql4 RecQ protein-like 4 gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1317097 Recql4 RecQ protein-like 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12915449 1317097 Recql4 RecQ protein-like 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12915449 1317097 Recql4 RecQ protein-like 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12915449 1317097 Recql4 RecQ protein-like 4 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15703196 1317097 Recql4 RecQ protein-like 4 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15703196 1317097 Recql4 RecQ protein-like 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15703196 1317097 Recql4 RecQ protein-like 4 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15703196 1317097 Recql4 RecQ protein-like 4 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:15703196 1317097 Recql4 RecQ protein-like 4 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:15703196 1317097 Recql4 RecQ protein-like 4 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11979727 1317097 Recql4 RecQ protein-like 4 gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12915449 1317097 Recql4 RecQ protein-like 4 gene MP:0005174 abnormal tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15703196 1317097 Recql4 RecQ protein-like 4 gene MP:0005359 growth retardation of incisors IAGP N RGD:5509061 20141003 MGI PMID:12915449 1317097 Recql4 RecQ protein-like 4 gene MP:0005655 increased aggression IEA N RGD:5509061 20230601 MGI 1317097 Recql4 RecQ protein-like 4 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:12915449 1317097 Recql4 RecQ protein-like 4 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:12915449 1317097 Recql4 RecQ protein-like 4 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:15703196 1317097 Recql4 RecQ protein-like 4 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15703196 1317097 Recql4 RecQ protein-like 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12915449 1317097 Recql4 RecQ protein-like 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12915449 1317097 Recql4 RecQ protein-like 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15703196 1317097 Recql4 RecQ protein-like 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11979727 1317097 Recql4 RecQ protein-like 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317097 Recql4 RecQ protein-like 4 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:11979727 1317097 Recql4 RecQ protein-like 4 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15703196 1317097 Recql4 RecQ protein-like 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1317097 Recql4 RecQ protein-like 4 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:15703196 1317101 Tbx1 T-box 1 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0000022 abnormal ear shape IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:15084464 1317101 Tbx1 T-box 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:19247433 1317101 Tbx1 T-box 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:24009395 1317101 Tbx1 T-box 1 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 1317101 Tbx1 T-box 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20191010 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:12913075 1317101 Tbx1 T-box 1 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0000040 absent middle ear ossicles IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0000040 absent middle ear ossicles IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20191010 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20191010 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:12913075 1317101 Tbx1 T-box 1 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:19247433 1317101 Tbx1 T-box 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19247433 1317101 Tbx1 T-box 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22921202 1317101 Tbx1 T-box 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16556915 1317101 Tbx1 T-box 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15175244 1317101 Tbx1 T-box 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20231109 MGI PMID:34050709 1317101 Tbx1 T-box 1 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:16556915 1317101 Tbx1 T-box 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:16556915 1317101 Tbx1 T-box 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:23971992 1317101 Tbx1 T-box 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231109 MGI PMID:34050709 1317101 Tbx1 T-box 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:22921202 1317101 Tbx1 T-box 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:19247433 1317101 Tbx1 T-box 1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:15175244 1317101 Tbx1 T-box 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:22921202 1317101 Tbx1 T-box 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:15385444 1317101 Tbx1 T-box 1 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0001068 abnormal mandibular nerve branching IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0001068 abnormal mandibular nerve branching IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0001072 abnormal vestibulocochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0001075 abnormal accessory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0001075 abnormal accessory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 1317101 Tbx1 T-box 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230119 MGI 1317101 Tbx1 T-box 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1317101 Tbx1 T-box 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:24009395 1317101 Tbx1 T-box 1 gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:22219655 1317101 Tbx1 T-box 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:24009395 1317101 Tbx1 T-box 1 gene MP:0001410 head bobbing IEA N RGD:5509061 20191010 MGI 1317101 Tbx1 T-box 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:20439995 1317101 Tbx1 T-box 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:16556915 1317101 Tbx1 T-box 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23011393 1317101 Tbx1 T-box 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230119 MGI 1317101 Tbx1 T-box 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20439995 1317101 Tbx1 T-box 1 gene MP:0001785 edema IEA N RGD:5509061 20170413 MGI 1317101 Tbx1 T-box 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:20439995 1317101 Tbx1 T-box 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12223416 1317101 Tbx1 T-box 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20439995 1317101 Tbx1 T-box 1 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20230119 MGI 1317101 Tbx1 T-box 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0001967 deafness IAGP N RGD:5509061 20191010 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1317101 Tbx1 T-box 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:21908517 1317101 Tbx1 T-box 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1317101 Tbx1 T-box 1 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 1317101 Tbx1 T-box 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:21177346 1317101 Tbx1 T-box 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:22921202 1317101 Tbx1 T-box 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15175244 1317101 Tbx1 T-box 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19247433 1317101 Tbx1 T-box 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21107579 1317101 Tbx1 T-box 1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:12913075 1317101 Tbx1 T-box 1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:19247433 1317101 Tbx1 T-box 1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0002253 abnormal pharyngeal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19531352 1317101 Tbx1 T-box 1 gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0002263 abnormal laryngeal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15385444 1317101 Tbx1 T-box 1 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20191010 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:21908517 1317101 Tbx1 T-box 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15175244 1317101 Tbx1 T-box 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:19247433 1317101 Tbx1 T-box 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317101 Tbx1 T-box 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:23971992 1317101 Tbx1 T-box 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11242049 1317101 Tbx1 T-box 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12464426 1317101 Tbx1 T-box 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15175244 1317101 Tbx1 T-box 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:19247433 1317101 Tbx1 T-box 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23011393 1317101 Tbx1 T-box 1 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16556915 1317101 Tbx1 T-box 1 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:21908517 1317101 Tbx1 T-box 1 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15084464 1317101 Tbx1 T-box 1 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20191010 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20191010 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11242049 1317101 Tbx1 T-box 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15175244 1317101 Tbx1 T-box 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:21364285 1317101 Tbx1 T-box 1 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0003142 anotia IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0003142 anotia IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0003147 absent cochlea IAGP N RGD:5509061 20141003 MGI PMID:12913075 1317101 Tbx1 T-box 1 gene MP:0003147 absent cochlea IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0003147 absent cochlea IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0003395 abnormal subclavian artery morphology IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0003410 abnormal artery development IAGP N RGD:5509061 20141003 MGI PMID:23011393 1317101 Tbx1 T-box 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:21908517 1317101 Tbx1 T-box 1 gene MP:0003679 ear lobe hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12913075 1317101 Tbx1 T-box 1 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:22921202 1317101 Tbx1 T-box 1 gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23011393 1317101 Tbx1 T-box 1 gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:21107579 1317101 Tbx1 T-box 1 gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1317101 Tbx1 T-box 1 gene MP:0004038 lymphangiectasis IAGP N RGD:5509061 20141003 MGI PMID:20439995 1317101 Tbx1 T-box 1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:12223416 1317101 Tbx1 T-box 1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15175244 1317101 Tbx1 T-box 1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:22921202 1317101 Tbx1 T-box 1 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:11239417 1317101 Tbx1 T-box 1 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15789410 1317101 Tbx1 T-box 1 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:12223416 1317101 Tbx1 T-box 1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0004159 double aortic arch IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0004159 double aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0004159 double aortic arch IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:11239417 1317101 Tbx1 T-box 1 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:22921202 1317101 Tbx1 T-box 1 gene MP:0004161 cervical aortic arch IAGP N RGD:5509061 20141003 MGI PMID:11239417 1317101 Tbx1 T-box 1 gene MP:0004161 cervical aortic arch IAGP N RGD:5509061 20141003 MGI PMID:12223416 1317101 Tbx1 T-box 1 gene MP:0004161 cervical aortic arch IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0004236 absent masseter muscle IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0004236 absent masseter muscle IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0004238 absent pterygoid muscle IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0004238 absent pterygoid muscle IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:24009395 1317101 Tbx1 T-box 1 gene MP:0004300 abnormal organ of Corti supporting cell morphology IAGP N RGD:5509061 20191010 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:12913075 1317101 Tbx1 T-box 1 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0004311 otic vesicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15084464 1317101 Tbx1 T-box 1 gene MP:0004311 otic vesicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0004314 absent inner ear vestibule IAGP N RGD:5509061 20141003 MGI PMID:12913075 1317101 Tbx1 T-box 1 gene MP:0004314 absent inner ear vestibule IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0004314 absent inner ear vestibule IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0004329 vestibular saccular degeneration IAGP N RGD:5509061 20141003 MGI PMID:24009395 1317101 Tbx1 T-box 1 gene MP:0004332 utricular degeneration IAGP N RGD:5509061 20141003 MGI PMID:24009395 1317101 Tbx1 T-box 1 gene MP:0004366 abnormal strial marginal cell morphology IAGP N RGD:5509061 20191010 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0004424 temporal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0004555 pharynx hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0004555 pharynx hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0004555 pharynx hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0004568 fusion of glossopharyngeal and vagus nerve IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0004569 glossopharyngeal nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0004569 glossopharyngeal nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0004572 fusion of basioccipital and basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0004572 fusion of basioccipital and basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0004572 fusion of basioccipital and basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0004572 fusion of basioccipital and basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0004612 fusion of vertebral bodies IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0004668 absent vertebral body IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20191010 MGI 1317101 Tbx1 T-box 1 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0004758 absent strial marginal cells IAGP N RGD:5509061 20191010 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:15175244 1317101 Tbx1 T-box 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:11242049 1317101 Tbx1 T-box 1 gene MP:0004790 absent upper incisors IAGP N RGD:5509061 20170928 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0004900 absent zygomatic arch IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0004914 absent ultimobranchial body IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0004922 abnormal common crus morphology IAGP N RGD:5509061 20191010 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:22219655 1317101 Tbx1 T-box 1 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16556915 1317101 Tbx1 T-box 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22921202 1317101 Tbx1 T-box 1 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 1317101 Tbx1 T-box 1 gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:24009395 1317101 Tbx1 T-box 1 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20191010 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20141003 MGI PMID:21177346 1317101 Tbx1 T-box 1 gene MP:0006033 abnormal external auditory canal morphology IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20439995 1317101 Tbx1 T-box 1 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 1317101 Tbx1 T-box 1 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16556915 1317101 Tbx1 T-box 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231109 MGI PMID:34050709 1317101 Tbx1 T-box 1 gene MP:0006285 absent inner ear IAGP N RGD:5509061 20141003 MGI PMID:12913075 1317101 Tbx1 T-box 1 gene MP:0006285 absent inner ear IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0006286 inner ear hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0006286 inner ear hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0006289 otic capsule hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0006339 abnormal third pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0006339 abnormal third pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0006340 abnormal fourth pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0006340 abnormal fourth pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0006340 abnormal fourth pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:21177346 1317101 Tbx1 T-box 1 gene MP:0006340 abnormal fourth pharyngeal arch morphology IAGP N RGD:5509061 20171116 MGI PMID:12858556 1317101 Tbx1 T-box 1 gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11242049 1317101 Tbx1 T-box 1 gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:21177346 1317101 Tbx1 T-box 1 gene MP:0006347 abnormal sixth pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11242049 1317101 Tbx1 T-box 1 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12223416 1317101 Tbx1 T-box 1 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12858556 1317101 Tbx1 T-box 1 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23011393 1317101 Tbx1 T-box 1 gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11242049 1317101 Tbx1 T-box 1 gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11242049 1317101 Tbx1 T-box 1 gene MP:0008304 abnormal organ of Corti supporting cell differentiation IAGP N RGD:5509061 20191010 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0008308 small scala media IAGP N RGD:5509061 20191010 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:21908517 1317101 Tbx1 T-box 1 gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20191010 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20439995 1317101 Tbx1 T-box 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:16684884 1317101 Tbx1 T-box 1 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20221006 MGI PMID:26689739 1317101 Tbx1 T-box 1 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221006 MGI PMID:26689739 1317101 Tbx1 T-box 1 gene MP:0009879 abnormal arcus anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:12858556 1317101 Tbx1 T-box 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:12858556 1317101 Tbx1 T-box 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15175244 1317101 Tbx1 T-box 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0009899 hyoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15084464 1317101 Tbx1 T-box 1 gene MP:0010241 abnormal aortic arch development IAGP N RGD:5509061 20141003 MGI PMID:12223416 1317101 Tbx1 T-box 1 gene MP:0010241 abnormal aortic arch development IAGP N RGD:5509061 20141003 MGI PMID:15789410 1317101 Tbx1 T-box 1 gene MP:0010326 malleus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0010328 thin malleus neck IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0010356 abnormal second pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11242049 1317101 Tbx1 T-box 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15175244 1317101 Tbx1 T-box 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16556915 1317101 Tbx1 T-box 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:22921202 1317101 Tbx1 T-box 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23971992 1317101 Tbx1 T-box 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:16556915 1317101 Tbx1 T-box 1 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15789410 1317101 Tbx1 T-box 1 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:34050709 1317101 Tbx1 T-box 1 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15789410 1317101 Tbx1 T-box 1 gene MP:0010425 abnormal heart and great vessel attachment IAGP N RGD:5509061 20141003 MGI PMID:16556915 1317101 Tbx1 T-box 1 gene MP:0010440 anomalous pulmonary venous connection IAGP N RGD:5509061 20141003 MGI PMID:16556915 1317101 Tbx1 T-box 1 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0010459 supravalvar pulmonary trunk stenosis IAGP N RGD:5509061 20141003 MGI PMID:16556915 1317101 Tbx1 T-box 1 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:11239417 1317101 Tbx1 T-box 1 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:15789410 1317101 Tbx1 T-box 1 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0010487 abnormal right subclavian artery morphology IAGP N RGD:5509061 20231109 MGI PMID:34050709 1317101 Tbx1 T-box 1 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16556915 1317101 Tbx1 T-box 1 gene MP:0010583 abnormal conotruncus morphology IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0010584 abnormal conotruncus septation IAGP N RGD:5509061 20141003 MGI PMID:11971873 1317101 Tbx1 T-box 1 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:16556915 1317101 Tbx1 T-box 1 gene MP:0010642 absent third pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11242049 1317101 Tbx1 T-box 1 gene MP:0010642 absent third pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15652707 1317101 Tbx1 T-box 1 gene MP:0010642 absent third pharyngeal arch IAGP N RGD:5509061 20171109 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0010643 absent fourth pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11242049 1317101 Tbx1 T-box 1 gene MP:0010643 absent fourth pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0010644 absent sixth pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11242049 1317101 Tbx1 T-box 1 gene MP:0010644 absent sixth pharyngeal arch IAGP N RGD:5509061 20171109 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0010729 absent arcus anterior IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20439995 1317101 Tbx1 T-box 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23971992 1317101 Tbx1 T-box 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16556915 1317101 Tbx1 T-box 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1317101 Tbx1 T-box 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22921202 1317101 Tbx1 T-box 1 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20141003 MGI PMID:22921202 1317101 Tbx1 T-box 1 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:12223416 1317101 Tbx1 T-box 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15190012 1317101 Tbx1 T-box 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20191017 MGI PMID:31550482 1317101 Tbx1 T-box 1 gene MP:0012080 chylous ascites IAGP N RGD:5509061 20141003 MGI PMID:20439995 1317101 Tbx1 T-box 1 gene MP:0012493 absent pharyngeal arch arteries IAGP N RGD:5509061 20141003 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0012721 short neck IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0012757 abnormal cranial neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0013174 pharynx stenosis IAGP N RGD:5509061 20141003 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0013265 abnormal fourth pharyngeal pouch morphology IAGP N RGD:5509061 20150101 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0013268 second pharyngeal arch hypoplasia IAGP N RGD:5509061 20171109 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0013270 fourth pharyngeal arch hypoplasia IAGP N RGD:5509061 20171116 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0014516 abnormal middle ear development IAGP N RGD:5509061 20240912 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:21908517 1317101 Tbx1 T-box 1 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:26689739 1317101 Tbx1 T-box 1 gene MP:0030040 absent facial muscle IAGP N RGD:5509061 20170914 MGI PMID:16452092 1317101 Tbx1 T-box 1 gene MP:0030137 abnormal upper incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0030228 absent tubotympanic recess IAGP N RGD:5509061 20171019 MGI PMID:16600992 1317101 Tbx1 T-box 1 gene MP:0030334 absent sixth pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:11242049 1317101 Tbx1 T-box 1 gene MP:0030334 absent sixth pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0030335 absent third pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:11242049 1317101 Tbx1 T-box 1 gene MP:0030335 absent third pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0030340 absent fourth pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:11242049 1317101 Tbx1 T-box 1 gene MP:0030340 absent fourth pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:15175244 1317101 Tbx1 T-box 1 gene MP:0030340 absent fourth pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:16914493 1317101 Tbx1 T-box 1 gene MP:0030340 absent fourth pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0030341 fourth pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20171116 MGI PMID:12858556 1317101 Tbx1 T-box 1 gene MP:0030341 fourth pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20171116 MGI PMID:15175244 1317101 Tbx1 T-box 1 gene MP:0030341 fourth pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20171116 MGI PMID:16696966 1317101 Tbx1 T-box 1 gene MP:0030341 fourth pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20171116 MGI PMID:19855134 1317101 Tbx1 T-box 1 gene MP:0030535 abnormal hypoglossal cord morphology IAGP N RGD:5509061 20180125 MGI PMID:15385444 1317101 Tbx1 T-box 1 gene MP:0030867 small thyroid cartilage IAGP N RGD:5509061 20181101 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0030872 small cricoid cartilage IAGP N RGD:5509061 20181101 MGI PMID:11242110 1317101 Tbx1 T-box 1 gene MP:0030872 small cricoid cartilage IAGP N RGD:5509061 20181101 MGI PMID:15469978 1317101 Tbx1 T-box 1 gene MP:0031461 abnormal palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:26689739 1317101 Tbx1 T-box 1 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:26689739 1317101 Tbx1 T-box 1 gene MP:0031463 increased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:26689739 1317101 Tbx1 T-box 1 gene MP:0031510 increased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:23011393 1317105 Syngr4 synaptogyrin 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1317106 Zfp54 zinc finger protein 54 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20201022 MGI 1317109 Natd1 N-acetyltransferase domain containing 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160421 MGI 1317109 Natd1 N-acetyltransferase domain containing 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 1317109 Natd1 N-acetyltransferase domain containing 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20200402 MGI 1317113 Pappa pregnancy-associated plasma protein A gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:14973274 1317113 Pappa pregnancy-associated plasma protein A gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20210930 MGI PMID:33905568 1317113 Pappa pregnancy-associated plasma protein A gene MP:0001127 small ovary IAGP N RGD:5509061 20220519 MGI PMID:20130263 1317113 Pappa pregnancy-associated plasma protein A gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:14973274 1317113 Pappa pregnancy-associated plasma protein A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14973274 1317113 Pappa pregnancy-associated plasma protein A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220519 MGI PMID:20130263 1317113 Pappa pregnancy-associated plasma protein A gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220519 MGI PMID:20130263 1317113 Pappa pregnancy-associated plasma protein A gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220519 MGI PMID:20130263 1317113 Pappa pregnancy-associated plasma protein A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23748359 1317113 Pappa pregnancy-associated plasma protein A gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 1317113 Pappa pregnancy-associated plasma protein A gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20190418 MGI 1317113 Pappa pregnancy-associated plasma protein A gene MP:0004692 small pubis IAGP N RGD:5509061 20210930 MGI PMID:33905568 1317113 Pappa pregnancy-associated plasma protein A gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220519 MGI PMID:20130263 1317113 Pappa pregnancy-associated plasma protein A gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:23748359 1317113 Pappa pregnancy-associated plasma protein A gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20220519 MGI PMID:20130263 1317113 Pappa pregnancy-associated plasma protein A gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20220519 MGI PMID:20130263 1317113 Pappa pregnancy-associated plasma protein A gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20220519 MGI PMID:20130263 1317113 Pappa pregnancy-associated plasma protein A gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20220519 MGI PMID:20130263 1317113 Pappa pregnancy-associated plasma protein A gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20220519 MGI PMID:20130263 1317113 Pappa pregnancy-associated plasma protein A gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:14973274 1317113 Pappa pregnancy-associated plasma protein A gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:14973274 1317113 Pappa pregnancy-associated plasma protein A gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20190418 MGI 1317113 Pappa pregnancy-associated plasma protein A gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 1317113 Pappa pregnancy-associated plasma protein A gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:20130263 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11877477 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22761313 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11877477 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11877477 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11877477 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0002494 increased IgM level IEA N RGD:5509061 20180222 MGI 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0004978 decreased B-1 B cell number IEA N RGD:5509061 20190404 MGI 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12833156 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12833156 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20201022 MGI 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0008168 decreased B-1a cell number IEA N RGD:5509061 20180222 MGI 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20180222 MGI 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:12833156 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0008203 absent B-1a cells IAGP N RGD:5509061 20141003 MGI PMID:12833156 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11877477 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:11877477 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11877477 1317116 Pik3ap1 phosphoinositide-3-kinase adaptor protein 1 gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20180222 MGI 1317117 Cep131 centrosomal protein 131 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20151231 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20220428 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20151231 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0001925 male infertility IAGP N RGD:5509061 20151231 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20151231 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20151231 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20151231 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220428 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20151231 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20151231 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20151231 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20151231 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220428 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220428 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20151231 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20151231 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20160204 MGI PMID:24415959 1317117 Cep131 centrosomal protein 131 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220428 MGI PMID:24415959 1317122 Exoc3l4 exocyst complex component 3-like 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1317124 Nedd1 neural precursor cell expressed, developmentally down-regulated gene 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 1317124 Nedd1 neural precursor cell expressed, developmentally down-regulated gene 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20200514 MGI 1317124 Nedd1 neural precursor cell expressed, developmentally down-regulated gene 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20211021 MGI 1317124 Nedd1 neural precursor cell expressed, developmentally down-regulated gene 1 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1317124 Nedd1 neural precursor cell expressed, developmentally down-regulated gene 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317124 Nedd1 neural precursor cell expressed, developmentally down-regulated gene 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1317128 Wipi1 WD repeat domain, phosphoinositide interacting 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1317128 Wipi1 WD repeat domain, phosphoinositide interacting 1 gene MP:0000601 small liver IEA N RGD:5509061 20230119 MGI 1317128 Wipi1 WD repeat domain, phosphoinositide interacting 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1317128 Wipi1 WD repeat domain, phosphoinositide interacting 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1317128 Wipi1 WD repeat domain, phosphoinositide interacting 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1317128 Wipi1 WD repeat domain, phosphoinositide interacting 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1317128 Wipi1 WD repeat domain, phosphoinositide interacting 1 gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 1317129 Nepn nephrocan gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20231207 MGI 1317132 Sphk2 sphingosine kinase 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17363629 1317132 Sphk2 sphingosine kinase 2 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20026661 1317132 Sphk2 sphingosine kinase 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20026661 1317132 Sphk2 sphingosine kinase 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23995678 1317132 Sphk2 sphingosine kinase 2 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17363629 1317132 Sphk2 sphingosine kinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:20026661 1317132 Sphk2 sphingosine kinase 2 gene MP:0002392 abnormal Peyer's patch T cell area morphology IAGP N RGD:5509061 20141003 MGI PMID:20026661 1317132 Sphk2 sphingosine kinase 2 gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:17363629 1317132 Sphk2 sphingosine kinase 2 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:23995678 1317132 Sphk2 sphingosine kinase 2 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:20026661 1317132 Sphk2 sphingosine kinase 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16223773 1317132 Sphk2 sphingosine kinase 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17363629 1317132 Sphk2 sphingosine kinase 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20026661 1317132 Sphk2 sphingosine kinase 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17363629 1317132 Sphk2 sphingosine kinase 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20026661 1317132 Sphk2 sphingosine kinase 2 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17947634 1317132 Sphk2 sphingosine kinase 2 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19808259 1317132 Sphk2 sphingosine kinase 2 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19808259 1317132 Sphk2 sphingosine kinase 2 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19808259 1317132 Sphk2 sphingosine kinase 2 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:17363629 1317132 Sphk2 sphingosine kinase 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16093248 1317132 Sphk2 sphingosine kinase 2 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:20026661 1317132 Sphk2 sphingosine kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0012503 increased midbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:16314531 1317132 Sphk2 sphingosine kinase 2 gene MP:0014470 abnormal B cell migration IAGP N RGD:5509061 20240613 MGI PMID:16223773 1317134 Aprt adenine phosphoribosyl transferase gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:9689017 1317134 Aprt adenine phosphoribosyl transferase gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:16105024 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16105024 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:8643571 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:9689017 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9776749 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230119 MGI 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:9776749 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:8643571 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:9776749 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:8643571 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:9689017 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:8643571 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:9776749 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:8643571 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:9776749 1317134 Aprt adenine phosphoribosyl transferase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16105024 1317134 Aprt adenine phosphoribosyl transferase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8643571 1317134 Aprt adenine phosphoribosyl transferase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9776749 1317134 Aprt adenine phosphoribosyl transferase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16105024 1317134 Aprt adenine phosphoribosyl transferase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:9776749 1317134 Aprt adenine phosphoribosyl transferase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:8643571 1317134 Aprt adenine phosphoribosyl transferase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0002708 nephrolithiasis IAGP N RGD:5509061 20141003 MGI PMID:11532086 1317134 Aprt adenine phosphoribosyl transferase gene MP:0002708 nephrolithiasis IAGP N RGD:5509061 20141003 MGI PMID:8643571 1317134 Aprt adenine phosphoribosyl transferase gene MP:0002708 nephrolithiasis IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0002708 nephrolithiasis IAGP N RGD:5509061 20141003 MGI PMID:9689017 1317134 Aprt adenine phosphoribosyl transferase gene MP:0002708 nephrolithiasis IAGP N RGD:5509061 20141003 MGI PMID:9776749 1317134 Aprt adenine phosphoribosyl transferase gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11532086 1317134 Aprt adenine phosphoribosyl transferase gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:8643571 1317134 Aprt adenine phosphoribosyl transferase gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:9776749 1317134 Aprt adenine phosphoribosyl transferase gene MP:0003670 dilated renal glomerular capsule IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:9689017 1317134 Aprt adenine phosphoribosyl transferase gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:8643571 1317134 Aprt adenine phosphoribosyl transferase gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9776749 1317134 Aprt adenine phosphoribosyl transferase gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:8643571 1317134 Aprt adenine phosphoribosyl transferase gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:9689017 1317134 Aprt adenine phosphoribosyl transferase gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:9689017 1317134 Aprt adenine phosphoribosyl transferase gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:9689017 1317134 Aprt adenine phosphoribosyl transferase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:9689017 1317134 Aprt adenine phosphoribosyl transferase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0009645 crystalluria IAGP N RGD:5509061 20141003 MGI PMID:9689017 1317134 Aprt adenine phosphoribosyl transferase gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20230601 MGI 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9776749 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:11532086 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011403 pyelonephritis IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011413 colorless urine IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011422 kidney medulla atrophy IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011424 decreased urine uric acid level IAGP N RGD:5509061 20141003 MGI PMID:8643571 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011477 abnormal urine nucleoside level IAGP N RGD:5509061 20141003 MGI PMID:16105024 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011477 abnormal urine nucleoside level IAGP N RGD:5509061 20141003 MGI PMID:8643571 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011477 abnormal urine nucleoside level IAGP N RGD:5509061 20141003 MGI PMID:8864750 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011625 cystolithiasis IAGP N RGD:5509061 20141003 MGI PMID:11532086 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011625 cystolithiasis IAGP N RGD:5509061 20141003 MGI PMID:8643571 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011844 kidney collecting duct atrophy IAGP N RGD:5509061 20141003 MGI PMID:11532086 1317134 Aprt adenine phosphoribosyl transferase gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:9689017 1317136 Nemf nuclear export mediator factor gene MP:0000958 peripheral nervous system degeneration IAGP N RGD:5509061 20210715 MGI PMID:32934225 1317136 Nemf nuclear export mediator factor gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20210722 MGI PMID:32934225 1317136 Nemf nuclear export mediator factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210722 MGI PMID:32934225 1317136 Nemf nuclear export mediator factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20210715 MGI PMID:32934225 1317136 Nemf nuclear export mediator factor gene MP:0001406 abnormal gait IAGP N RGD:5509061 20210715 MGI PMID:32934225 1317136 Nemf nuclear export mediator factor gene MP:0001954 respiratory distress IAGP N RGD:5509061 20220120 MGI PMID:32934225 1317136 Nemf nuclear export mediator factor gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20181227 MGI 1317136 Nemf nuclear export mediator factor gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20210715 MGI PMID:32934225 1317136 Nemf nuclear export mediator factor gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20210722 MGI PMID:32934225 1317136 Nemf nuclear export mediator factor gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1317136 Nemf nuclear export mediator factor gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20210715 MGI PMID:32934225 1317136 Nemf nuclear export mediator factor gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1317136 Nemf nuclear export mediator factor gene MP:0005405 axon degeneration IAGP N RGD:5509061 20210722 MGI PMID:32934225 1317136 Nemf nuclear export mediator factor gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1317136 Nemf nuclear export mediator factor gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20210715 MGI PMID:32934225 1317136 Nemf nuclear export mediator factor gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20210722 MGI PMID:32934225 1317136 Nemf nuclear export mediator factor gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20210722 MGI PMID:32934225 1317136 Nemf nuclear export mediator factor gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20220120 MGI PMID:32934225 1317136 Nemf nuclear export mediator factor gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20210722 MGI PMID:32934225 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0001203 increased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:12660172 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16061652 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141030 MGI PMID:23620591 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:16061652 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:16061652 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16061652 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16061652 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16061652 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141030 MGI PMID:23620591 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141030 MGI PMID:23620591 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:16061652 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:16061652 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:16061652 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12660172 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:12660172 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141030 MGI PMID:23620591 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12660172 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:16061652 1317139 Hmgn1 high mobility group nucleosomal binding domain 1 gene MP:0011940 decreased food intake IEA N RGD:5509061 20211021 MGI 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:11566878 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11566878 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11566878 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20200514 MGI 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11566878 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11566878 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11566878 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20160915 MGI PMID:25203538 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0003660 chylothorax IAGP N RGD:5509061 20141003 MGI PMID:11566878 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0003660 chylothorax IAGP N RGD:5509061 20160915 MGI PMID:25203538 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0004038 lymphangiectasis IAGP N RGD:5509061 20141003 MGI PMID:11566878 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20160915 MGI PMID:25203538 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20160915 MGI PMID:25203538 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20160915 MGI PMID:25203538 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0010820 abnormal pleura morphology IAGP N RGD:5509061 20141003 MGI PMID:11566878 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11566878 1317144 Elk3 ELK3, member of ETS oncogene family gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160915 MGI PMID:25203538 1317146 Cmtm6 CKLF-like MARVEL transmembrane domain containing 6 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20210401 MGI PMID:32908139 1317146 Cmtm6 CKLF-like MARVEL transmembrane domain containing 6 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20210401 MGI PMID:32908139 1317146 Cmtm6 CKLF-like MARVEL transmembrane domain containing 6 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20210401 MGI PMID:32908139 1317146 Cmtm6 CKLF-like MARVEL transmembrane domain containing 6 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20210401 MGI PMID:32908139 1317146 Cmtm6 CKLF-like MARVEL transmembrane domain containing 6 gene MP:0005572 abnormal pulmonary respiratory rate IAGP N RGD:5509061 20210401 MGI PMID:32908139 1317146 Cmtm6 CKLF-like MARVEL transmembrane domain containing 6 gene MP:0011994 increased nerve conduction velocity IAGP N RGD:5509061 20210401 MGI PMID:32908139 1317148 Gan giant axonal neuropathy gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16303566 1317148 Gan giant axonal neuropathy gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:16565160 1317148 Gan giant axonal neuropathy gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:16565160 1317148 Gan giant axonal neuropathy gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:16565160 1317148 Gan giant axonal neuropathy gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:18680552 1317148 Gan giant axonal neuropathy gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16565160 1317148 Gan giant axonal neuropathy gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16565160 1317148 Gan giant axonal neuropathy gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:16565160 1317148 Gan giant axonal neuropathy gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16565160 1317148 Gan giant axonal neuropathy gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16565160 1317148 Gan giant axonal neuropathy gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:16565160 1317148 Gan giant axonal neuropathy gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:18680552 1317148 Gan giant axonal neuropathy gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16565160 1317148 Gan giant axonal neuropathy gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:18680552 1317148 Gan giant axonal neuropathy gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:16565160 1317148 Gan giant axonal neuropathy gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:18680552 1317148 Gan giant axonal neuropathy gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:16565160 1317148 Gan giant axonal neuropathy gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:16565160 1317151 Tm9sf4 transmembrane 9 superfamily member 4 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20211021 MGI 1317151 Tm9sf4 transmembrane 9 superfamily member 4 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 1317151 Tm9sf4 transmembrane 9 superfamily member 4 gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 1317151 Tm9sf4 transmembrane 9 superfamily member 4 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1317151 Tm9sf4 transmembrane 9 superfamily member 4 gene MP:0003036 vertebral transformation IEA N RGD:5509061 20141003 MGI 1317151 Tm9sf4 transmembrane 9 superfamily member 4 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1317151 Tm9sf4 transmembrane 9 superfamily member 4 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 1317151 Tm9sf4 transmembrane 9 superfamily member 4 gene MP:0010099 abnormal thoracic cage shape IEA N RGD:5509061 20150430 MGI 1317151 Tm9sf4 transmembrane 9 superfamily member 4 gene MP:0012725 small sebaceous gland IAGP N RGD:5509061 20150709 MGI PMID:24721909 1317153 Ttc8 tetratricopeptide repeat domain 8 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:21646512 1317153 Ttc8 tetratricopeptide repeat domain 8 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21646512 1317153 Ttc8 tetratricopeptide repeat domain 8 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:21646512 1317153 Ttc8 tetratricopeptide repeat domain 8 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:21646512 1317153 Ttc8 tetratricopeptide repeat domain 8 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:21646512 1317153 Ttc8 tetratricopeptide repeat domain 8 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21646512 1317153 Ttc8 tetratricopeptide repeat domain 8 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21646512 1317153 Ttc8 tetratricopeptide repeat domain 8 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:21646512 1317153 Ttc8 tetratricopeptide repeat domain 8 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:21646512 1317153 Ttc8 tetratricopeptide repeat domain 8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21646512 1317153 Ttc8 tetratricopeptide repeat domain 8 gene MP:0011281 abnormal olfactory epithelium cilium morphology IAGP N RGD:5509061 20160407 MGI PMID:21646512 1317155 Gga1 golgi associated, gamma adaptin ear containing, ARF binding protein 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:22291915 1317155 Gga1 golgi associated, gamma adaptin ear containing, ARF binding protein 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1317155 Gga1 golgi associated, gamma adaptin ear containing, ARF binding protein 1 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1317155 Gga1 golgi associated, gamma adaptin ear containing, ARF binding protein 1 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:22291915 1317155 Gga1 golgi associated, gamma adaptin ear containing, ARF binding protein 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:22291915 1317155 Gga1 golgi associated, gamma adaptin ear containing, ARF binding protein 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1317155 Gga1 golgi associated, gamma adaptin ear containing, ARF binding protein 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1317155 Gga1 golgi associated, gamma adaptin ear containing, ARF binding protein 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:22291915 1317155 Gga1 golgi associated, gamma adaptin ear containing, ARF binding protein 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:22291915 1317155 Gga1 golgi associated, gamma adaptin ear containing, ARF binding protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22291915 1317155 Gga1 golgi associated, gamma adaptin ear containing, ARF binding protein 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22291915 1317156 Wiz widely-interspaced zinc finger motifs gene MP:0000111 cleft palate IAGP N RGD:5509061 20220721 MGI PMID:34150743 1317156 Wiz widely-interspaced zinc finger motifs gene MP:0000445 short snout IAGP N RGD:5509061 20220721 MGI PMID:34150743 1317156 Wiz widely-interspaced zinc finger motifs gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1317156 Wiz widely-interspaced zinc finger motifs gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20220811 MGI 1317156 Wiz widely-interspaced zinc finger motifs gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20220721 MGI PMID:34150743 1317156 Wiz widely-interspaced zinc finger motifs gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20220519 MGI 1317156 Wiz widely-interspaced zinc finger motifs gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20220721 MGI PMID:34150743 1317156 Wiz widely-interspaced zinc finger motifs gene MP:0010099 abnormal thoracic cage shape IEA N RGD:5509061 20220811 MGI 1317156 Wiz widely-interspaced zinc finger motifs gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20220721 MGI PMID:34150743 1317156 Wiz widely-interspaced zinc finger motifs gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24025402 1317156 Wiz widely-interspaced zinc finger motifs gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1317156 Wiz widely-interspaced zinc finger motifs gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20220721 MGI PMID:34150743 1317156 Wiz widely-interspaced zinc finger motifs gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20141003 MGI PMID:24025402 1317156 Wiz widely-interspaced zinc finger motifs gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20220721 MGI PMID:34150743 1317160 Nup37 nucleoporin 37 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20240523 MGI 1317160 Nup37 nucleoporin 37 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1317160 Nup37 nucleoporin 37 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20181227 MGI 1317160 Nup37 nucleoporin 37 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220519 MGI 1317164 Opalin oligodendrocytic myelin paranodal and inner loop protein gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20190926 MGI PMID:27855200 1317166 Rbms1 RNA binding motif, single stranded interacting protein 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1317166 Rbms1 RNA binding motif, single stranded interacting protein 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20181227 MGI 1317166 Rbms1 RNA binding motif, single stranded interacting protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11737267 1317166 Rbms1 RNA binding motif, single stranded interacting protein 1 gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:11737267 1317166 Rbms1 RNA binding motif, single stranded interacting protein 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1317166 Rbms1 RNA binding motif, single stranded interacting protein 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1317166 Rbms1 RNA binding motif, single stranded interacting protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11737267 1317166 Rbms1 RNA binding motif, single stranded interacting protein 1 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:11737267 1317166 Rbms1 RNA binding motif, single stranded interacting protein 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220811 MGI 1317166 Rbms1 RNA binding motif, single stranded interacting protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317166 Rbms1 RNA binding motif, single stranded interacting protein 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11737267 1317166 Rbms1 RNA binding motif, single stranded interacting protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11737267 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:15121860 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0000650 mesocardia IAGP N RGD:5509061 20141003 MGI PMID:15121860 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15121860 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15121860 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0001967 deafness IAGP N RGD:5509061 20170907 MGI PMID:26469318 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15121860 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:15121860 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0004131 abnormal motile primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:15121860 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15121860 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:15121860 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20170907 MGI PMID:26469318 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20170907 MGI PMID:26469318 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0004403 absent cochlear outer hair cells IAGP N RGD:5509061 20170907 MGI PMID:26469318 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20170907 MGI PMID:26469318 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0005330 cardiomyopathy IEA N RGD:5509061 20141003 MGI 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20170907 MGI PMID:26469318 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0006325 impaired hearing IAGP N RGD:5509061 20170907 MGI PMID:26469318 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15121860 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141003 MGI 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0011061 abnormal inner hair cell kinocilium morphology IAGP N RGD:5509061 20170907 MGI PMID:26469318 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15121860 1317169 Rfx3 regulatory factor X, 3 (influences HLA class II expression) gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15121860 1317173 Cdkn3 cyclin dependent kinase inhibitor 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1317173 Cdkn3 cyclin dependent kinase inhibitor 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1317176 Ccne2 cyclin E2 gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12970191 1317176 Ccne2 cyclin E2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:21944720 1317176 Ccne2 cyclin E2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21944720 1317176 Ccne2 cyclin E2 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:12970191 1317176 Ccne2 cyclin E2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21944720 1317176 Ccne2 cyclin E2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12970191 1317176 Ccne2 cyclin E2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12970191 1317176 Ccne2 cyclin E2 gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:12970191 1317176 Ccne2 cyclin E2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12970191 1317176 Ccne2 cyclin E2 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:12970191 1317176 Ccne2 cyclin E2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21944720 1317176 Ccne2 cyclin E2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12970191 1317176 Ccne2 cyclin E2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:21944720 1317176 Ccne2 cyclin E2 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12970191 1317176 Ccne2 cyclin E2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12970191 1317176 Ccne2 cyclin E2 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12970191 1317176 Ccne2 cyclin E2 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:21944720 1317176 Ccne2 cyclin E2 gene MP:0010241 abnormal aortic arch development IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12970191 1317176 Ccne2 cyclin E2 gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:21944720 1317176 Ccne2 cyclin E2 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:12941272 1317176 Ccne2 cyclin E2 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20180301 MGI PMID:21944720 1317178 Prpf4b pre-mRNA processing factor 4B gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20241017 MGI 1317178 Prpf4b pre-mRNA processing factor 4B gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20191205 MGI 1317178 Prpf4b pre-mRNA processing factor 4B gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241017 MGI 1317178 Prpf4b pre-mRNA processing factor 4B gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20191205 MGI 1317178 Prpf4b pre-mRNA processing factor 4B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317178 Prpf4b pre-mRNA processing factor 4B gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20191205 MGI 1317178 Prpf4b pre-mRNA processing factor 4B gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1317178 Prpf4b pre-mRNA processing factor 4B gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1317182 Snx20 sorting nexin 20 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18196517 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0000088 short mandible IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0000373 belly spot IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0000585 kinked tail IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0000692 small spleen IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0000705 athymia IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0000828 abnormal fourth ventricle morphology IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0000852 small cerebellum IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0000923 abnormal roof plate morphology IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0001258 decreased body length IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0001393 ataxia IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0001577 anemia IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0001921 reduced fertility IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0002764 short tibia IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0003051 curly tail IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0008409 increased cellular sensitivity to hydroxyurea IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0010250 absent thymus cortex IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0012504 increased forebrain apoptosis IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317191 Pole4 polymerase (DNA-directed), epsilon 4 (p12 subunit) gene MP:0030049 prominent forehead IAGP N RGD:5509061 20180712 MGI PMID:29754823 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20180125 MGI PMID:28737513 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16936253 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0001260 increased body weight IEA N RGD:5509061 20141003 MGI 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180517 MGI PMID:28737513 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16936253 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180125 MGI PMID:28737513 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16936253 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0002083 premature death IAGP N RGD:5509061 20180125 MGI PMID:28737513 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:16936253 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20180125 MGI PMID:28737513 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20180125 MGI PMID:28737513 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20180125 MGI PMID:28737513 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16936253 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:16936253 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20180531 MGI PMID:16936253 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20180125 MGI PMID:28737513 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:16936253 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20180125 MGI PMID:28737513 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20180125 MGI PMID:28737513 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:16936253 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20160804 MGI 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18840758 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20180517 MGI PMID:28737513 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20180125 MGI PMID:28737513 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20180125 MGI PMID:28737513 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20190711 MGI PMID:28737513 1317193 Bag3 BCL2-associated athanogene 3 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:28737513 1317195 Zfyve1 zinc finger, FYVE domain containing 1 gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20200924 MGI PMID:32251420 1317195 Zfyve1 zinc finger, FYVE domain containing 1 gene MP:0009790 decreased susceptibility to viral infection induced morbidity/mortality IAGP N RGD:5509061 20200924 MGI PMID:32251420 1317197 Igsf3 immunoglobulin superfamily, member 3 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20240516 MGI PMID:37821496 1317197 Igsf3 immunoglobulin superfamily, member 3 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20240516 MGI PMID:37821496 1317197 Igsf3 immunoglobulin superfamily, member 3 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20240516 MGI PMID:37821496 1317197 Igsf3 immunoglobulin superfamily, member 3 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20240516 MGI PMID:37821496 1317197 Igsf3 immunoglobulin superfamily, member 3 gene MP:0008802 abnormal intestinal smooth muscle morphology IAGP N RGD:5509061 20240516 MGI PMID:37821496 1317197 Igsf3 immunoglobulin superfamily, member 3 gene MP:0013007 abnormal vagal neural crest cell migration IAGP N RGD:5509061 20240516 MGI PMID:37821496 1317201 Ist1 increased sodium tolerance 1 homolog (yeast) gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1317201 Ist1 increased sodium tolerance 1 homolog (yeast) gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210520 MGI 1317201 Ist1 increased sodium tolerance 1 homolog (yeast) gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210520 MGI 1317201 Ist1 increased sodium tolerance 1 homolog (yeast) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317203 Apobec3 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16055735 1317203 Apobec3 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:18772436 1317203 Apobec3 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:286744 1317203 Apobec3 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3 gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:17259974 1317203 Apobec3 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3 gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:18772436 1317203 Apobec3 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3 gene MP:0020935 decreased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:286744 1317203 Apobec3 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3 gene MP:0031038 increased susceptibility to Retroviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:18772436 1317205 Cmtr1 cap methyltransferase 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220519 MGI 1317205 Cmtr1 cap methyltransferase 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20210211 MGI PMID:33086056 1317205 Cmtr1 cap methyltransferase 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20210211 MGI PMID:33086056 1317205 Cmtr1 cap methyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317205 Cmtr1 cap methyltransferase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1317205 Cmtr1 cap methyltransferase 1 gene MP:0020069 decreased neocortex size IAGP N RGD:5509061 20210211 MGI PMID:33086056 1317205 Cmtr1 cap methyltransferase 1 gene MP:0020912 abnormal susceptibility to Riboviria infection IAGP N RGD:5509061 20210211 MGI PMID:33086056 1317207 Noxo1 NADPH oxidase organizer 1 gene MP:0001394 circling IEA N RGD:5509061 20111116 MGI 1317207 Noxo1 NADPH oxidase organizer 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:16431374 1317207 Noxo1 NADPH oxidase organizer 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16431374 1317207 Noxo1 NADPH oxidase organizer 1 gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:16431374 1317207 Noxo1 NADPH oxidase organizer 1 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:16431374 1317207 Noxo1 NADPH oxidase organizer 1 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:16431374 1317208 Herc3 hect domain and RLD 3 gene MP:0000745 tremors IEA N RGD:5509061 20160804 MGI 1317208 Herc3 hect domain and RLD 3 gene MP:0001391 abnormal tail movements IEA N RGD:5509061 20160804 MGI 1317208 Herc3 hect domain and RLD 3 gene MP:0001512 trunk curl IEA N RGD:5509061 20160804 MGI 1317208 Herc3 hect domain and RLD 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1317208 Herc3 hect domain and RLD 3 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20160804 MGI 1317208 Herc3 hect domain and RLD 3 gene MP:0009759 abnormal hair follicle bulge morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:22615570 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22615570 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20191226 MGI PMID:26263558 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20191226 MGI PMID:26263558 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20191226 MGI PMID:26263558 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20191226 MGI PMID:26263558 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:24014876 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:24014876 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:24014876 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:24014876 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0008648 decreased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:24014876 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:24014876 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20220421 MGI PMID:22615570 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:24014876 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0020155 enhanced humoral immune response IAGP N RGD:5509061 20191226 MGI PMID:26263558 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:22615570 1317210 Ifit2 interferon-induced protein with tetratricopeptide repeats 2 gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:22615570 1317212 Fam209 family with sequence similarity 209 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1317212 Fam209 family with sequence similarity 209 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220224 MGI PMID:34471926 1317212 Fam209 family with sequence similarity 209 gene MP:0001925 male infertility IAGP N RGD:5509061 20220224 MGI PMID:34471926 1317212 Fam209 family with sequence similarity 209 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220224 MGI PMID:34471926 1317212 Fam209 family with sequence similarity 209 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220224 MGI PMID:34471926 1317212 Fam209 family with sequence similarity 209 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20220224 MGI PMID:34471926 1317212 Fam209 family with sequence similarity 209 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220224 MGI PMID:34471926 1317215 Rnf19a ring finger protein 19A gene MP:0001399 hyperactivity IAGP N RGD:5509061 20180712 MGI PMID:26553645 1317215 Rnf19a ring finger protein 19A gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20180712 MGI PMID:26553645 1317215 Rnf19a ring finger protein 19A gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20180712 MGI PMID:26553645 1317215 Rnf19a ring finger protein 19A gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20180712 MGI PMID:26553645 1317215 Rnf19a ring finger protein 19A gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20180712 MGI PMID:26553645 1317215 Rnf19a ring finger protein 19A gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20180712 MGI PMID:26553645 1317215 Rnf19a ring finger protein 19A gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20180712 MGI PMID:26553645 1317217 Efna4 ephrin A4 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20181227 MGI 1317217 Efna4 ephrin A4 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1317217 Efna4 ephrin A4 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20181227 MGI 1317217 Efna4 ephrin A4 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20220519 MGI 1317217 Efna4 ephrin A4 gene MP:0011471 decreased urine creatinine level IEA N RGD:5509061 20240523 MGI 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20171214 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9626504 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0003840 abnormal coronal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0004420 parietal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0030189 broad snout IAGP N RGD:5509061 20171019 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0030387 large posterior fontanelle IAGP N RGD:5509061 20171214 MGI PMID:17567669 1317221 Itgb1bp1 integrin beta 1 binding protein 1 gene MP:0030431 wide metopic suture IAGP N RGD:5509061 20171214 MGI PMID:17567669 1317223 Supt20 SPT20 SAGA complex component gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0002174 abnormal gastrulation movements IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0005224 abnormal left-right axis symmetry of the somites IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0011257 abnormal head fold morphology IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317223 Supt20 SPT20 SAGA complex component gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:16751104 1317225 Dnajc10 DnaJ heat shock protein family (Hsp40) member C10 gene MP:0001258 decreased body length IEA N RGD:5509061 20170323 MGI 1317225 Dnajc10 DnaJ heat shock protein family (Hsp40) member C10 gene MP:0001262 decreased body weight IEA N RGD:5509061 20170323 MGI 1317225 Dnajc10 DnaJ heat shock protein family (Hsp40) member C10 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20170323 MGI 1317225 Dnajc10 DnaJ heat shock protein family (Hsp40) member C10 gene MP:0005310 abnormal salivary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:19788412 1317225 Dnajc10 DnaJ heat shock protein family (Hsp40) member C10 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 1317225 Dnajc10 DnaJ heat shock protein family (Hsp40) member C10 gene MP:0012322 decreased total tissue mass IEA N RGD:5509061 20170323 MGI 1317225 Dnajc10 DnaJ heat shock protein family (Hsp40) member C10 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20161013 MGI PMID:19788412 1317231 Gas8 growth arrest specific 8 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20161103 MGI PMID:27472056 1317231 Gas8 growth arrest specific 8 gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20161103 MGI PMID:27472056 1317231 Gas8 growth arrest specific 8 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20161103 MGI PMID:27472056 1317231 Gas8 growth arrest specific 8 gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20161103 MGI PMID:27472056 1317231 Gas8 growth arrest specific 8 gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20161103 MGI PMID:27472056 1317231 Gas8 growth arrest specific 8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20161103 MGI PMID:27472056 1317231 Gas8 growth arrest specific 8 gene MP:0011253 situs inversus with levocardia IAGP N RGD:5509061 20161103 MGI PMID:27472056 1317233 Hint1 histidine triad nucleotide binding protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12810953 1317233 Hint1 histidine triad nucleotide binding protein 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12748294 1317233 Hint1 histidine triad nucleotide binding protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12748294 1317233 Hint1 histidine triad nucleotide binding protein 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20160804 MGI 1317233 Hint1 histidine triad nucleotide binding protein 1 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:12810953 1317233 Hint1 histidine triad nucleotide binding protein 1 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20211104 MGI PMID:33953175 1317233 Hint1 histidine triad nucleotide binding protein 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:12810953 1317233 Hint1 histidine triad nucleotide binding protein 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 1317233 Hint1 histidine triad nucleotide binding protein 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:12810953 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0000160 kyphosis IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0000745 tremors IAGP N RGD:5509061 20160929 MGI PMID:27534441 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0001393 ataxia IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0002804 abnormal motor learning IEA N RGD:5509061 20211021 MGI 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0002946 delayed axon extension IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20160929 MGI PMID:27534441 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20220519 MGI 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0011874 enlarged urinary bladder IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317237 Zfyve26 zinc finger, FYVE domain containing 26 gene MP:0012506 brain atrophy IAGP N RGD:5509061 20160304 MGI PMID:24367272 1317246 Kif13a kinesin family member 13A gene MP:0000445 short snout IAGP N RGD:5509061 20200130 MGI PMID:31487503 1317246 Kif13a kinesin family member 13A gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1317246 Kif13a kinesin family member 13A gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1317246 Kif13a kinesin family member 13A gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1317246 Kif13a kinesin family member 13A gene MP:0001148 enlarged testis IEA N RGD:5509061 20210826 MGI 1317246 Kif13a kinesin family member 13A gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1317246 Kif13a kinesin family member 13A gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23438369 1317246 Kif13a kinesin family member 13A gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1317246 Kif13a kinesin family member 13A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23438369 1317246 Kif13a kinesin family member 13A gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210826 MGI 1317246 Kif13a kinesin family member 13A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1317246 Kif13a kinesin family member 13A gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1317246 Kif13a kinesin family member 13A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200130 MGI PMID:31487503 1317246 Kif13a kinesin family member 13A gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1317246 Kif13a kinesin family member 13A gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:23438369 1317246 Kif13a kinesin family member 13A gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 1317246 Kif13a kinesin family member 13A gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1317246 Kif13a kinesin family member 13A gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23438369 1317246 Kif13a kinesin family member 13A gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210826 MGI 1317246 Kif13a kinesin family member 13A gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20200130 MGI PMID:31487503 1317246 Kif13a kinesin family member 13A gene MP:0009709 hydrometra IEA N RGD:5509061 20220811 MGI 1317246 Kif13a kinesin family member 13A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200130 MGI PMID:31487503 1317250 Nup133 nucleoporin 133 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18539113 1317250 Nup133 nucleoporin 133 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:18539113 1317250 Nup133 nucleoporin 133 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18539113 1317250 Nup133 nucleoporin 133 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:18539113 1317250 Nup133 nucleoporin 133 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15755804 1317250 Nup133 nucleoporin 133 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:18539113 1317250 Nup133 nucleoporin 133 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18539113 1317250 Nup133 nucleoporin 133 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:18539113 1317250 Nup133 nucleoporin 133 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:18539113 1317250 Nup133 nucleoporin 133 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:18539113 1317250 Nup133 nucleoporin 133 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:18539113 1317250 Nup133 nucleoporin 133 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18539113 1317250 Nup133 nucleoporin 133 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 1317250 Nup133 nucleoporin 133 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18539113 1317250 Nup133 nucleoporin 133 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317250 Nup133 nucleoporin 133 gene MP:0012183 decreased paraxial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:15755804 1317250 Nup133 nucleoporin 133 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1317252 Irf7 interferon regulatory factor 7 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1317252 Irf7 interferon regulatory factor 7 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20351692 1317252 Irf7 interferon regulatory factor 7 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15800576 1317252 Irf7 interferon regulatory factor 7 gene MP:0008563 decreased interferon-alpha secretion IEA N RGD:5509061 20111116 MGI 1317252 Irf7 interferon regulatory factor 7 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20351692 1317252 Irf7 interferon regulatory factor 7 gene MP:0008576 decreased circulating interferon-beta level IEA N RGD:5509061 20150305 MGI 1317252 Irf7 interferon regulatory factor 7 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20351692 1317252 Irf7 interferon regulatory factor 7 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:15800576 1317252 Irf7 interferon regulatory factor 7 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:15800576 1317252 Irf7 interferon regulatory factor 7 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:20351692 1317252 Irf7 interferon regulatory factor 7 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:15800576 1317252 Irf7 interferon regulatory factor 7 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:26329040 1317252 Irf7 interferon regulatory factor 7 gene MP:0020952 increased susceptibility to Paramyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:20351692 1317252 Irf7 interferon regulatory factor 7 gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:26329040 1317256 Nelfb negative elongation factor complex member B gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:19340312 1317256 Nelfb negative elongation factor complex member B gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:19340312 1317256 Nelfb negative elongation factor complex member B gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:19340312 1317256 Nelfb negative elongation factor complex member B gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19340312 1317256 Nelfb negative elongation factor complex member B gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19340312 1317256 Nelfb negative elongation factor complex member B gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19340312 1317258 Nrsn1 neurensin 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1317258 Nrsn1 neurensin 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1317258 Nrsn1 neurensin 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201231 MGI 1317258 Nrsn1 neurensin 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1317258 Nrsn1 neurensin 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1317258 Nrsn1 neurensin 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1317264 Zfp212 Zinc finger protein 212 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20211216 MGI PMID:34815492 1317264 Zfp212 Zinc finger protein 212 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20211216 MGI PMID:34815492 1317264 Zfp212 Zinc finger protein 212 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20211216 MGI PMID:34815492 1317264 Zfp212 Zinc finger protein 212 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20211216 MGI PMID:34815492 1317264 Zfp212 Zinc finger protein 212 gene MP:0002083 premature death IAGP N RGD:5509061 20211216 MGI PMID:34815492 1317264 Zfp212 Zinc finger protein 212 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20211216 MGI PMID:34815492 1317264 Zfp212 Zinc finger protein 212 gene MP:0020870 decreased thigmotaxis IAGP N RGD:5509061 20211216 MGI PMID:34815492 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15936750 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15936750 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20231221 MGI PMID:15936750 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12482960 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:14993236 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12482960 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:14993236 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20240104 MGI PMID:15936750 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0002748 abnormal pulmonary valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0009408 decreased skeletal muscle fiber density IAGP N RGD:5509061 20141003 MGI PMID:12482960 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15936750 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0010620 thick mitral valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0010620 thick mitral valve IAGP N RGD:5509061 20231221 MGI PMID:15936750 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0010629 thick tricuspid valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12482960 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15936750 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0031558 tricuspid valve hyperplasia IAGP N RGD:5509061 20240104 MGI PMID:15936750 1317266 Adam12 ADAM metallopeptidase domain 12 gene MP:0031581 semilunar valve hyperplasia IAGP N RGD:5509061 20240125 MGI PMID:15936750 1317268 Scaper S phase cyclin A-associated protein in the ER gene MP:0001147 small testis IAGP N RGD:5509061 20201022 MGI PMID:32510560 1317268 Scaper S phase cyclin A-associated protein in the ER gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20201022 MGI PMID:32510560 1317268 Scaper S phase cyclin A-associated protein in the ER gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20201022 MGI PMID:32510560 1317268 Scaper S phase cyclin A-associated protein in the ER gene MP:0001925 male infertility IAGP N RGD:5509061 20201022 MGI PMID:32510560 1317268 Scaper S phase cyclin A-associated protein in the ER gene MP:0001935 decreased litter size IAGP N RGD:5509061 20201022 MGI PMID:32510560 1317268 Scaper S phase cyclin A-associated protein in the ER gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20201022 MGI PMID:32510560 1317268 Scaper S phase cyclin A-associated protein in the ER gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20201022 MGI PMID:32510560 1317268 Scaper S phase cyclin A-associated protein in the ER gene MP:0005159 azoospermia IAGP N RGD:5509061 20201022 MGI PMID:32510560 1317268 Scaper S phase cyclin A-associated protein in the ER gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1317268 Scaper S phase cyclin A-associated protein in the ER gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1317268 Scaper S phase cyclin A-associated protein in the ER gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1317268 Scaper S phase cyclin A-associated protein in the ER gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20201022 MGI PMID:32510560 1317268 Scaper S phase cyclin A-associated protein in the ER gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20201022 MGI PMID:32510560 1317268 Scaper S phase cyclin A-associated protein in the ER gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:32510560 1317271 Mfap4 microfibrillar-associated protein 4 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1317271 Mfap4 microfibrillar-associated protein 4 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20160818 MGI PMID:26033354 1317271 Mfap4 microfibrillar-associated protein 4 gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20160818 MGI PMID:26033354 1317271 Mfap4 microfibrillar-associated protein 4 gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20160818 MGI PMID:26033354 1317271 Mfap4 microfibrillar-associated protein 4 gene MP:0010901 abnormal pulmonary alveolar parenchyma morphology IAGP N RGD:5509061 20160818 MGI PMID:26033354 1317271 Mfap4 microfibrillar-associated protein 4 gene MP:0010937 increased total lung capacity IAGP N RGD:5509061 20160818 MGI PMID:26033354 1317271 Mfap4 microfibrillar-associated protein 4 gene MP:0011045 decreased lung elastance IAGP N RGD:5509061 20160818 MGI PMID:26033354 1317274 Pias1 protein inhibitor of activated STAT 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15311277 1317274 Pias1 protein inhibitor of activated STAT 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:15311277 1317274 Pias1 protein inhibitor of activated STAT 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15311277 1317274 Pias1 protein inhibitor of activated STAT 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15311277 1317274 Pias1 protein inhibitor of activated STAT 1 gene MP:0031023 decreased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:15311277 1317275 Trak1 trafficking protein, kinesin binding 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16380713 1317275 Trak1 trafficking protein, kinesin binding 1 gene MP:0000746 weakness IEA N RGD:5509061 20111116 MGI 1317275 Trak1 trafficking protein, kinesin binding 1 gene MP:0001405 impaired coordination IEA N RGD:5509061 20111116 MGI 1317275 Trak1 trafficking protein, kinesin binding 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16380713 1317275 Trak1 trafficking protein, kinesin binding 1 gene MP:0001504 abnormal posture IEA N RGD:5509061 20111116 MGI 1317275 Trak1 trafficking protein, kinesin binding 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:16380713 1317275 Trak1 trafficking protein, kinesin binding 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16380713 1317275 Trak1 trafficking protein, kinesin binding 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:16380713 1317275 Trak1 trafficking protein, kinesin binding 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16380713 1317275 Trak1 trafficking protein, kinesin binding 1 gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:16380713 1317277 Ldlrad3 low density lipoprotein receptor class A domain containing 3 gene MP:0020941 decreased susceptibility to Togaviridae infection IAGP N RGD:5509061 20210325 MGI PMID:33208938 1317281 Usp33 ubiquitin specific peptidase 33 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1317281 Usp33 ubiquitin specific peptidase 33 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 1317281 Usp33 ubiquitin specific peptidase 33 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20160804 MGI 1317281 Usp33 ubiquitin specific peptidase 33 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20160804 MGI 1317281 Usp33 ubiquitin specific peptidase 33 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1317281 Usp33 ubiquitin specific peptidase 33 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1317283 Zfp395 zinc finger protein 395 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200402 MGI 1317283 Zfp395 zinc finger protein 395 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1317283 Zfp395 zinc finger protein 395 gene MP:0010571 shortened ST segment IEA N RGD:5509061 20200402 MGI 1317283 Zfp395 zinc finger protein 395 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20200402 MGI 1317288 Gpr87 G protein-coupled receptor 87 gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20141003 MGI 1317288 Gpr87 G protein-coupled receptor 87 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1317288 Gpr87 G protein-coupled receptor 87 gene MP:0004610 small vertebrae IEA N RGD:5509061 20141003 MGI 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20231207 MGI 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20240523 MGI 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20231207 MGI 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0000692 small spleen IEA N RGD:5509061 20231207 MGI 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20170420 MGI PMID:28355569 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0000745 tremors IAGP N RGD:5509061 20170420 MGI PMID:28355569 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:22144914 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20170420 MGI PMID:28355569 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20170420 MGI PMID:28355569 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:16982418 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:22144914 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20160331 MGI PMID:26985035 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20170420 MGI PMID:28355569 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20200402 MGI PMID:31557132 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22144914 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200402 MGI PMID:31557132 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170420 MGI PMID:28355569 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20231207 MGI 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0001732 postnatal growth retardation IEA N RGD:5509061 20111116 MGI 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20240523 MGI 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22144914 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16982418 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16982418 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:16982418 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20200402 MGI PMID:31557132 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:16982418 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20160331 MGI PMID:26985035 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20160331 MGI PMID:26985035 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:22144914 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20160331 MGI PMID:26985035 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:16982418 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:16982418 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:16982418 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22144914 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20170420 MGI PMID:28355569 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200402 MGI PMID:31557132 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:16982418 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20200402 MGI PMID:31557132 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:22144914 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20170420 MGI PMID:28355569 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20200402 MGI PMID:31557132 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20170420 MGI PMID:28355569 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0009428 decreased tibialis anterior weight IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:22144914 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160331 MGI PMID:26985035 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200402 MGI PMID:31557132 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22144914 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16982418 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19470612 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22144914 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20240523 MGI 1317293 Gars1 glycyl-tRNA synthetase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20231207 MGI 1317295 Rnf121 ring finger protein 121 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20240523 MGI 1317297 Trim29 tripartite motif-containing 29 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317297 Trim29 tripartite motif-containing 29 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317297 Trim29 tripartite motif-containing 29 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160421 MGI 1317297 Trim29 tripartite motif-containing 29 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317297 Trim29 tripartite motif-containing 29 gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317297 Trim29 tripartite motif-containing 29 gene MP:0008562 increased interferon-alpha secretion IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317297 Trim29 tripartite motif-containing 29 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317297 Trim29 tripartite motif-containing 29 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317297 Trim29 tripartite motif-containing 29 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317297 Trim29 tripartite motif-containing 29 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 1317297 Trim29 tripartite motif-containing 29 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1317297 Trim29 tripartite motif-containing 29 gene MP:0010091 decreased circulating creatine kinase level IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317297 Trim29 tripartite motif-containing 29 gene MP:0011393 decreased fetal cardiomyocyte apoptosis IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317297 Trim29 tripartite motif-containing 29 gene MP:0012416 decreased gland tumor incidence IAGP N RGD:5509061 20241024 MGI PMID:31048544 1317297 Trim29 tripartite motif-containing 29 gene MP:0013662 decreased myeloid cell number IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317297 Trim29 tripartite motif-containing 29 gene MP:0014435 increased interferon level IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317297 Trim29 tripartite motif-containing 29 gene MP:0014438 decreased interleukin level IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317297 Trim29 tripartite motif-containing 29 gene MP:0020938 decreased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317297 Trim29 tripartite motif-containing 29 gene MP:0031039 decreased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317297 Trim29 tripartite motif-containing 29 gene MP:0031601 decreased endoplasmic reticulum stress IAGP N RGD:5509061 20240718 MGI PMID:38664417 1317298 Fbxw16 F-box and WD-40 domain protein 16 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1317298 Fbxw16 F-box and WD-40 domain protein 16 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1317298 Fbxw16 F-box and WD-40 domain protein 16 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1317298 Fbxw16 F-box and WD-40 domain protein 16 gene MP:0000706 small thymus IEA N RGD:5509061 20210128 MGI 1317298 Fbxw16 F-box and WD-40 domain protein 16 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1317298 Fbxw16 F-box and WD-40 domain protein 16 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210128 MGI 1317298 Fbxw16 F-box and WD-40 domain protein 16 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20210128 MGI 1317298 Fbxw16 F-box and WD-40 domain protein 16 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1317298 Fbxw16 F-box and WD-40 domain protein 16 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1317298 Fbxw16 F-box and WD-40 domain protein 16 gene MP:0013436 increased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20210826 MGI 1317300 Napb N-ethylmaleimide sensitive fusion protein attachment protein beta gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20201022 MGI 1317300 Napb N-ethylmaleimide sensitive fusion protein attachment protein beta gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21040848 1317300 Napb N-ethylmaleimide sensitive fusion protein attachment protein beta gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1317300 Napb N-ethylmaleimide sensitive fusion protein attachment protein beta gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1317300 Napb N-ethylmaleimide sensitive fusion protein attachment protein beta gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:21040848 1317300 Napb N-ethylmaleimide sensitive fusion protein attachment protein beta gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:21040848 1317300 Napb N-ethylmaleimide sensitive fusion protein attachment protein beta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21040848 1317300 Napb N-ethylmaleimide sensitive fusion protein attachment protein beta gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21040848 1317300 Napb N-ethylmaleimide sensitive fusion protein attachment protein beta gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:21040848 1317300 Napb N-ethylmaleimide sensitive fusion protein attachment protein beta gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21040848 1317300 Napb N-ethylmaleimide sensitive fusion protein attachment protein beta gene MP:0004924 abnormal behavior IEA N RGD:5509061 20190502 MGI 1317300 Napb N-ethylmaleimide sensitive fusion protein attachment protein beta gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1317300 Napb N-ethylmaleimide sensitive fusion protein attachment protein beta gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1317304 Pycr1 pyrroline-5-carboxylate reductase 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20240314 MGI PMID:33734376 1317304 Pycr1 pyrroline-5-carboxylate reductase 1 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20230601 MGI 1317304 Pycr1 pyrroline-5-carboxylate reductase 1 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20240509 MGI PMID:36495058 1317304 Pycr1 pyrroline-5-carboxylate reductase 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20240314 MGI PMID:33734376 1317304 Pycr1 pyrroline-5-carboxylate reductase 1 gene MP:0031216 decreased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20240509 MGI PMID:36495058 1317306 Gatb glutamyl-tRNA amidotransferase subunit B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1317315 Fbxo36 F-box protein 36 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20181227 MGI 1317315 Fbxo36 F-box protein 36 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210128 MGI 1317315 Fbxo36 F-box protein 36 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20210128 MGI 1317315 Fbxo36 F-box protein 36 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20181227 MGI 1317315 Fbxo36 F-box protein 36 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1317315 Fbxo36 F-box protein 36 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20210128 MGI 1317315 Fbxo36 F-box protein 36 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20181227 MGI 1317315 Fbxo36 F-box protein 36 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20211021 MGI 1317315 Fbxo36 F-box protein 36 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20181227 MGI 1317315 Fbxo36 F-box protein 36 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20181227 MGI 1317315 Fbxo36 F-box protein 36 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1317315 Fbxo36 F-box protein 36 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1317318 Sema4b sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4B gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:21270411 1317318 Sema4b sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4B gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:21270411 1317318 Sema4b sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4B gene MP:0004041 increased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20161201 MGI PMID:25892012 1317318 Sema4b sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4B gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:21270411 1317318 Sema4b sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4B gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20161201 MGI PMID:25892012 1317320 Slc30a7 solute carrier family 30 (zinc transporter), member 7 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20240523 MGI 1317320 Slc30a7 solute carrier family 30 (zinc transporter), member 7 gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20240523 MGI 1317320 Slc30a7 solute carrier family 30 (zinc transporter), member 7 gene MP:0001670 abnormal intestinal mineral absorption IAGP N RGD:5509061 20141003 MGI PMID:17954933 1317320 Slc30a7 solute carrier family 30 (zinc transporter), member 7 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20231207 MGI 1317320 Slc30a7 solute carrier family 30 (zinc transporter), member 7 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20240523 MGI 1317320 Slc30a7 solute carrier family 30 (zinc transporter), member 7 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17954933 1317320 Slc30a7 solute carrier family 30 (zinc transporter), member 7 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17954933 1317320 Slc30a7 solute carrier family 30 (zinc transporter), member 7 gene MP:0009615 abnormal zinc homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17954933 1317320 Slc30a7 solute carrier family 30 (zinc transporter), member 7 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1317320 Slc30a7 solute carrier family 30 (zinc transporter), member 7 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:17954933 1317320 Slc30a7 solute carrier family 30 (zinc transporter), member 7 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20220811 MGI 1317320 Slc30a7 solute carrier family 30 (zinc transporter), member 7 gene MP:0031172 decreased circulating zinc level IAGP N RGD:5509061 20201119 MGI PMID:17954933 1317325 Lactb2 lactamase, beta 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:12374767 1317325 Lactb2 lactamase, beta 2 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:12374767 1317325 Lactb2 lactamase, beta 2 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:12374767 1317325 Lactb2 lactamase, beta 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12374767 1317325 Lactb2 lactamase, beta 2 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:12374767 1317325 Lactb2 lactamase, beta 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12374767 1317325 Lactb2 lactamase, beta 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12374767 1317325 Lactb2 lactamase, beta 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12374767 1317325 Lactb2 lactamase, beta 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:12374767 1317325 Lactb2 lactamase, beta 2 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:12374767 1317325 Lactb2 lactamase, beta 2 gene MP:0013317 abnormal seminal vesicle development IAGP N RGD:5509061 20141204 MGI PMID:12374767 1317325 Lactb2 lactamase, beta 2 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:12374767 1317326 Prss54 serine protease 54 gene MP:0000160 kyphosis IEA N RGD:5509061 20210520 MGI 1317326 Prss54 serine protease 54 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1317326 Prss54 serine protease 54 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1317326 Prss54 serine protease 54 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1317326 Prss54 serine protease 54 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1317326 Prss54 serine protease 54 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220519 MGI 1317326 Prss54 serine protease 54 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20230202 MGI PMID:35863763 1317326 Prss54 serine protease 54 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20240523 MGI 1317326 Prss54 serine protease 54 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20210520 MGI 1317326 Prss54 serine protease 54 gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20240523 MGI 1317326 Prss54 serine protease 54 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20230202 MGI PMID:35863763 1317326 Prss54 serine protease 54 gene MP:0013519 decreased CD4-positive NK T cell number IEA N RGD:5509061 20240523 MGI 1317326 Prss54 serine protease 54 gene MP:0013522 decreased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20240523 MGI 1317326 Prss54 serine protease 54 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20230202 MGI PMID:35863763 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20180111 MGI PMID:27480224 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20191010 MGI PMID:26746789 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20180111 MGI PMID:27480224 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180111 MGI PMID:27480224 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20191010 MGI PMID:26746789 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0001914 hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180111 MGI PMID:27480224 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180111 MGI PMID:27480224 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20150416 MGI PMID:25066056 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20191010 MGI PMID:26746789 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20191010 MGI PMID:26746789 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20150416 MGI PMID:25066056 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20150416 MGI PMID:25066056 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180111 MGI PMID:27480224 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20180111 MGI PMID:27480224 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20180111 MGI PMID:27480224 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20180111 MGI PMID:27480224 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20150416 MGI PMID:25066056 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20191010 MGI PMID:26746789 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20191010 MGI PMID:26746789 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0011131 abnormal lung endothelial cell physiology IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0011140 decreased lung endothelial cell proliferation IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0011141 increased lung endothelial cell apoptosis IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0012201 decreased endothelial cell proliferation IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0013848 subcutaneous edema IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0020321 increased vascular endothelial cell apoptosis IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0020517 abnormal visceral yolk sac physiology IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317329 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit gene MP:0020830 abnormal jugular lymph sac morphology IAGP N RGD:5509061 20191010 MGI PMID:26755743 1317336 Fastkd2 FAST kinase domains 2 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200402 MGI 1317336 Fastkd2 FAST kinase domains 2 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220519 MGI 1317336 Fastkd2 FAST kinase domains 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1317336 Fastkd2 FAST kinase domains 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1317338 Twnk twinkle mtDNA helicase gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:23393161 1317338 Twnk twinkle mtDNA helicase gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:23393161 1317338 Twnk twinkle mtDNA helicase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23393161 1317338 Twnk twinkle mtDNA helicase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:23393161 1317338 Twnk twinkle mtDNA helicase gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:23393161 1317338 Twnk twinkle mtDNA helicase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23393161 1317338 Twnk twinkle mtDNA helicase gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23393161 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20826270 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:20826270 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0001788 periorbital edema IAGP N RGD:5509061 20141003 MGI PMID:20826270 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0002989 small kidney IEA N RGD:5509061 20181227 MGI 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0003390 lymphedema IAGP N RGD:5509061 20141003 MGI PMID:20826270 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0003604 single kidney IEA N RGD:5509061 20210520 MGI 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0004106 lymphatic vessel hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20826270 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20181227 MGI 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1317340 Ptpn14 protein tyrosine phosphatase, non-receptor type 14 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1317342 Ube2d1 ubiquitin-conjugating enzyme E2D 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1317342 Ube2d1 ubiquitin-conjugating enzyme E2D 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200514 MGI 1317342 Ube2d1 ubiquitin-conjugating enzyme E2D 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1317342 Ube2d1 ubiquitin-conjugating enzyme E2D 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1317343 Patl2 protein associated with topoisomerase II homolog 2 (yeast) gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20181011 MGI PMID:29661911 1317343 Patl2 protein associated with topoisomerase II homolog 2 (yeast) gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20181011 MGI PMID:29661911 1317343 Patl2 protein associated with topoisomerase II homolog 2 (yeast) gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20181011 MGI PMID:29661911 1317343 Patl2 protein associated with topoisomerase II homolog 2 (yeast) gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20181011 MGI PMID:29661911 1317343 Patl2 protein associated with topoisomerase II homolog 2 (yeast) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20181011 MGI PMID:29661911 1317343 Patl2 protein associated with topoisomerase II homolog 2 (yeast) gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20181011 MGI PMID:29661911 1317343 Patl2 protein associated with topoisomerase II homolog 2 (yeast) gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20181011 MGI PMID:29661911 1317343 Patl2 protein associated with topoisomerase II homolog 2 (yeast) gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20181011 MGI PMID:29661911 1317343 Patl2 protein associated with topoisomerase II homolog 2 (yeast) gene MP:0011120 increased primordial ovarian follicle number IAGP N RGD:5509061 20181011 MGI PMID:29661911 1317343 Patl2 protein associated with topoisomerase II homolog 2 (yeast) gene MP:0014447 impaired spindle assembly in female meiosis IAGP N RGD:5509061 20240509 MGI PMID:29661911 1317343 Patl2 protein associated with topoisomerase II homolog 2 (yeast) gene MP:0031014 polyspermy IAGP N RGD:5509061 20200130 MGI PMID:29661911 1317347 Mynn myoneurin gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1317347 Mynn myoneurin gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210520 MGI 1317347 Mynn myoneurin gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1317347 Mynn myoneurin gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1317347 Mynn myoneurin gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210826 MGI 1317350 Adipor2 adiponectin receptor 2 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20160414 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17068142 1317350 Adipor2 adiponectin receptor 2 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17068142 1317350 Adipor2 adiponectin receptor 2 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17268472 1317350 Adipor2 adiponectin receptor 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1317350 Adipor2 adiponectin receptor 2 gene MP:0001147 small testis IEA N RGD:5509061 20200402 MGI 1317350 Adipor2 adiponectin receptor 2 gene MP:0001154 seminiferous tubule degeneration IEA N RGD:5509061 20111116 MGI 1317350 Adipor2 adiponectin receptor 2 gene MP:0001156 abnormal spermatogenesis IEA N RGD:5509061 20111116 MGI 1317350 Adipor2 adiponectin receptor 2 gene MP:0001513 limb grasping IEA N RGD:5509061 20170105 MGI 1317350 Adipor2 adiponectin receptor 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17268472 1317350 Adipor2 adiponectin receptor 2 gene MP:0001925 male infertility IEA N RGD:5509061 20230601 MGI 1317350 Adipor2 adiponectin receptor 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17068142 1317350 Adipor2 adiponectin receptor 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17268472 1317350 Adipor2 adiponectin receptor 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17268472 1317350 Adipor2 adiponectin receptor 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17068142 1317350 Adipor2 adiponectin receptor 2 gene MP:0002687 oligozoospermia IEA N RGD:5509061 20111116 MGI 1317350 Adipor2 adiponectin receptor 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17068142 1317350 Adipor2 adiponectin receptor 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:17068142 1317350 Adipor2 adiponectin receptor 2 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:17268472 1317350 Adipor2 adiponectin receptor 2 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0004929 decreased epididymis weight IEA N RGD:5509061 20111116 MGI 1317350 Adipor2 adiponectin receptor 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1317350 Adipor2 adiponectin receptor 2 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17068142 1317350 Adipor2 adiponectin receptor 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17068142 1317350 Adipor2 adiponectin receptor 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17268472 1317350 Adipor2 adiponectin receptor 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17268472 1317350 Adipor2 adiponectin receptor 2 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17068142 1317350 Adipor2 adiponectin receptor 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17268472 1317350 Adipor2 adiponectin receptor 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17068142 1317350 Adipor2 adiponectin receptor 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20160414 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20160414 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0009303 decreased renal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17268472 1317350 Adipor2 adiponectin receptor 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1317350 Adipor2 adiponectin receptor 2 gene MP:0011019 abnormal adaptive thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:24531262 1317350 Adipor2 adiponectin receptor 2 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:24531262 1317350 Adipor2 adiponectin receptor 2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0020550 multinucleated giant male germ cells IEA N RGD:5509061 20180301 MGI 1317350 Adipor2 adiponectin receptor 2 gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:17068142 1317350 Adipor2 adiponectin receptor 2 gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:17327425 1317350 Adipor2 adiponectin receptor 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:17327425 1317356 Wee1 WEE 1 homolog 1 (S. pombe) gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20160218 MGI PMID:16810330 1317356 Wee1 WEE 1 homolog 1 (S. pombe) gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20160218 MGI PMID:16810330 1317356 Wee1 WEE 1 homolog 1 (S. pombe) gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1317356 Wee1 WEE 1 homolog 1 (S. pombe) gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20160218 MGI PMID:16810330 1317356 Wee1 WEE 1 homolog 1 (S. pombe) gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20181227 MGI 1317356 Wee1 WEE 1 homolog 1 (S. pombe) gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20221215 MGI 1317356 Wee1 WEE 1 homolog 1 (S. pombe) gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20160218 MGI PMID:16810330 1317356 Wee1 WEE 1 homolog 1 (S. pombe) gene MP:0006205 embryonic lethality between implantation and somite formation IEA N RGD:5509061 20141003 MGI 1317356 Wee1 WEE 1 homolog 1 (S. pombe) gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20160218 MGI PMID:16810330 1317356 Wee1 WEE 1 homolog 1 (S. pombe) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1317356 Wee1 WEE 1 homolog 1 (S. pombe) gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20160218 MGI PMID:16810330 1317356 Wee1 WEE 1 homolog 1 (S. pombe) gene MP:0011191 increased embryonic epiblast cell apoptosis IAGP N RGD:5509061 20160218 MGI PMID:16810330 1317356 Wee1 WEE 1 homolog 1 (S. pombe) gene MP:0011192 decreased embryonic epiblast cell proliferation IAGP N RGD:5509061 20160218 MGI PMID:16810330 1317356 Wee1 WEE 1 homolog 1 (S. pombe) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1317356 Wee1 WEE 1 homolog 1 (S. pombe) gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1317357 Clptm1l CLPTM1-like gene MP:0001304 cataract IEA N RGD:5509061 20210826 MGI 1317357 Clptm1l CLPTM1-like gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1317357 Clptm1l CLPTM1-like gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1317357 Clptm1l CLPTM1-like gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1317357 Clptm1l CLPTM1-like gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1317357 Clptm1l CLPTM1-like gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1317357 Clptm1l CLPTM1-like gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1317357 Clptm1l CLPTM1-like gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20190314 MGI PMID:30042348 1317357 Clptm1l CLPTM1-like gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20190314 MGI PMID:30042348 1317357 Clptm1l CLPTM1-like gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20181227 MGI 1317357 Clptm1l CLPTM1-like gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1317357 Clptm1l CLPTM1-like gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1317357 Clptm1l CLPTM1-like gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20190314 MGI PMID:30042348 1317357 Clptm1l CLPTM1-like gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20190314 MGI PMID:30042348 1317361 Serpina1f serine (or cysteine) peptidase inhibitor, clade A, member 1F gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1317361 Serpina1f serine (or cysteine) peptidase inhibitor, clade A, member 1F gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0000088 short mandible IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20180906 MGI PMID:28880886 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20180906 MGI PMID:28880886 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20150122 MGI PMID:20838829 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20150122 MGI PMID:20838829 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0000547 short limbs IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180906 MGI PMID:28880886 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20150122 MGI PMID:20838829 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20150122 MGI PMID:20838829 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0003109 short femur IAGP N RGD:5509061 20180906 MGI PMID:28880886 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0004338 small clavicle IAGP N RGD:5509061 20150122 MGI PMID:20838829 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20150122 MGI PMID:20838829 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20150122 MGI PMID:20838829 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0004374 bowed radius IAGP N RGD:5509061 20150122 MGI PMID:20838829 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0004374 bowed radius IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20150122 MGI PMID:20838829 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20150122 MGI PMID:20838829 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20150122 MGI PMID:20838829 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20180906 MGI PMID:28880886 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20180906 MGI PMID:28880886 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20180906 MGI PMID:28880886 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0010926 increased osteoid volume IAGP N RGD:5509061 20180906 MGI PMID:28880886 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20180906 MGI PMID:28880886 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0010969 absent compact bone IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20150122 MGI PMID:20838829 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20150122 MGI PMID:20838829 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0011585 decreased alkaline phosphatase activity IAGP N RGD:5509061 20180906 MGI PMID:28880886 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0011585 decreased alkaline phosphatase activity IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20180906 MGI PMID:28880886 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20180906 MGI PMID:29174564 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0030275 thin frontal bone IAGP N RGD:5509061 20171102 MGI PMID:20838829 1317362 Ifitm5 interferon induced transmembrane protein 5 gene MP:0030850 abnormal ilium body morphology IAGP N RGD:5509061 20181025 MGI PMID:20838829 1317367 Stxbp4 syntaxin binding protein 4 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210128 MGI 1317367 Stxbp4 syntaxin binding protein 4 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1317370 Kntc1 kinetochore associated 1 gene MP:0000585 kinked tail IEA N RGD:5509061 20150730 MGI 1317370 Kntc1 kinetochore associated 1 gene MP:0005287 narrow eye opening IEA N RGD:5509061 20201231 MGI 1317370 Kntc1 kinetochore associated 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1317370 Kntc1 kinetochore associated 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1317372 Tmem87b transmembrane protein 87B gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1317374 Ing5 inhibitor of growth family, member 5 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20240523 MGI 1317374 Ing5 inhibitor of growth family, member 5 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20240307 MGI PMID:37275850 1317374 Ing5 inhibitor of growth family, member 5 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20240307 MGI PMID:37275850 1317374 Ing5 inhibitor of growth family, member 5 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20240307 MGI PMID:37275850 1317374 Ing5 inhibitor of growth family, member 5 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20240307 MGI PMID:37275850 1317374 Ing5 inhibitor of growth family, member 5 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1317374 Ing5 inhibitor of growth family, member 5 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210520 MGI 1317374 Ing5 inhibitor of growth family, member 5 gene MP:0005542 cornea vascularization IEA N RGD:5509061 20240523 MGI 1317374 Ing5 inhibitor of growth family, member 5 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20221215 MGI 1317374 Ing5 inhibitor of growth family, member 5 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20240307 MGI PMID:37275850 1317374 Ing5 inhibitor of growth family, member 5 gene MP:0011243 decreased fetal derived definitive erythrocyte cell number IAGP N RGD:5509061 20240307 MGI PMID:37275850 1317374 Ing5 inhibitor of growth family, member 5 gene MP:0011246 abnormal fetal liver hematopoietic progenitor cell morphology IAGP N RGD:5509061 20240307 MGI PMID:37275850 1317374 Ing5 inhibitor of growth family, member 5 gene MP:0012121 sclerocornea IEA N RGD:5509061 20240523 MGI 1317374 Ing5 inhibitor of growth family, member 5 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210520 MGI 1317377 Pcbp4 poly(rC) binding protein 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20171207 MGI PMID:26915821 1317377 Pcbp4 poly(rC) binding protein 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20171207 MGI PMID:26915821 1317377 Pcbp4 poly(rC) binding protein 4 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20171207 MGI PMID:26915821 1317377 Pcbp4 poly(rC) binding protein 4 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20171207 MGI PMID:26915821 1317377 Pcbp4 poly(rC) binding protein 4 gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20171207 MGI PMID:26915821 1317377 Pcbp4 poly(rC) binding protein 4 gene MP:0010294 increased kidney tumor incidence IAGP N RGD:5509061 20171207 MGI PMID:26915821 1317377 Pcbp4 poly(rC) binding protein 4 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20171207 MGI PMID:26915821 1317379 Wbp11 WW domain binding protein 11 gene MP:0000111 cleft palate IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0000467 abnormal esophagus morphology IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0000601 small liver IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0002989 small kidney IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0003641 small lung IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0004600 abnormal vertebral transverse process morphology IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0008832 hemivertebra IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0008922 abnormal cervical rib IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0008970 choanal atresia IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0011854 cerebral edema IAGP N RGD:5509061 20210325 MGI PMID:33276377 1317379 Wbp11 WW domain binding protein 11 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:33276377 1317381 Phc2 polyhomeotic 2 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21059868 1317381 Phc2 polyhomeotic 2 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0000080 abnormal exoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:24091011 1317381 Phc2 polyhomeotic 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17215307 1317381 Phc2 polyhomeotic 2 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:24091011 1317381 Phc2 polyhomeotic 2 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0004342 scapular bone foramen IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:21059868 1317381 Phc2 polyhomeotic 2 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:24091011 1317381 Phc2 polyhomeotic 2 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:21059868 1317381 Phc2 polyhomeotic 2 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:24091011 1317381 Phc2 polyhomeotic 2 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:21059868 1317381 Phc2 polyhomeotic 2 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:24091011 1317381 Phc2 polyhomeotic 2 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:24091011 1317381 Phc2 polyhomeotic 2 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21059868 1317381 Phc2 polyhomeotic 2 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0006338 abnormal second pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21059868 1317381 Phc2 polyhomeotic 2 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0010701 fusion of atlas and odontoid process IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0010702 split cervical atlas IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0010703 split cervical axis IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21059868 1317381 Phc2 polyhomeotic 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317381 Phc2 polyhomeotic 2 gene MP:0012062 small tail bud IAGP N RGD:5509061 20141003 MGI PMID:16024804 1317383 Ints15 integrator complex subunit 15 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0001304 cataract IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0005098 abnormal optic choroid morphology IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0006182 increased retina hemangioma incidence IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0008259 abnormal optic disk morphology IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0009392 retina gliosis IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0021107 retina fold IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317383 Ints15 integrator complex subunit 15 gene MP:0031428 lens dislocation IAGP N RGD:5509061 20240523 MGI PMID:36851842 1317385 Ptdss2 phosphatidylserine synthase 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12361952 1317385 Ptdss2 phosphatidylserine synthase 2 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:12361952 1317385 Ptdss2 phosphatidylserine synthase 2 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12361952 1317385 Ptdss2 phosphatidylserine synthase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12361952 1317385 Ptdss2 phosphatidylserine synthase 2 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:12361952 1317385 Ptdss2 phosphatidylserine synthase 2 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:18343815 1317385 Ptdss2 phosphatidylserine synthase 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12361952 1317385 Ptdss2 phosphatidylserine synthase 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18343815 1317386 Ammecr1l AMME chromosomal region gene 1-like gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20231207 MGI 1317386 Ammecr1l AMME chromosomal region gene 1-like gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1317389 Mmp1a matrix metallopeptidase 1a (interstitial collagenase) gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23548910 1317389 Mmp1a matrix metallopeptidase 1a (interstitial collagenase) gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23548910 1317389 Mmp1a matrix metallopeptidase 1a (interstitial collagenase) gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:23548910 1317389 Mmp1a matrix metallopeptidase 1a (interstitial collagenase) gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23548910 1317389 Mmp1a matrix metallopeptidase 1a (interstitial collagenase) gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23548910 1317389 Mmp1a matrix metallopeptidase 1a (interstitial collagenase) gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:23548910 1317389 Mmp1a matrix metallopeptidase 1a (interstitial collagenase) gene MP:0008654 increased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:23548910 1317389 Mmp1a matrix metallopeptidase 1a (interstitial collagenase) gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:23548910 1317389 Mmp1a matrix metallopeptidase 1a (interstitial collagenase) gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:23548910 1317392 Mfap5 microfibrillar associated protein 5 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23963447 1317392 Mfap5 microfibrillar associated protein 5 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23963447 1317392 Mfap5 microfibrillar associated protein 5 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23963447 1317392 Mfap5 microfibrillar associated protein 5 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:23963447 1317392 Mfap5 microfibrillar associated protein 5 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23963447 1317392 Mfap5 microfibrillar associated protein 5 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23963447 1317392 Mfap5 microfibrillar associated protein 5 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23963447 1317392 Mfap5 microfibrillar associated protein 5 gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:23963447 1317392 Mfap5 microfibrillar associated protein 5 gene MP:0010963 abnormal compact bone volume IAGP N RGD:5509061 20141003 MGI PMID:23963447 1317394 Tbc1d15 TBC1 domain family, member 15 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20240620 MGI PMID:35680100 1317394 Tbc1d15 TBC1 domain family, member 15 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20240620 MGI PMID:35680100 1317394 Tbc1d15 TBC1 domain family, member 15 gene MP:0014239 abnormal intracellular organelle morphology IAGP N RGD:5509061 20240620 MGI PMID:35680100 1317394 Tbc1d15 TBC1 domain family, member 15 gene MP:0031217 increased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20240620 MGI PMID:35680100 1317396 Ldb2 LIM domain binding 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1317398 Tmem9 transmembrane protein 9 gene MP:0001661 extended life span IAGP N RGD:5509061 20211125 MGI PMID:30374053 1317398 Tmem9 transmembrane protein 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:30374053 1317398 Tmem9 transmembrane protein 9 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20211125 MGI PMID:30374053 1317398 Tmem9 transmembrane protein 9 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20211125 MGI PMID:30374053 1317398 Tmem9 transmembrane protein 9 gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20211125 MGI PMID:30374053 1317408 Lamp3 lysosomal-associated membrane protein 3 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210826 MGI 1317408 Lamp3 lysosomal-associated membrane protein 3 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20230302 MGI PMID:34161347 1317408 Lamp3 lysosomal-associated membrane protein 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1317408 Lamp3 lysosomal-associated membrane protein 3 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1317408 Lamp3 lysosomal-associated membrane protein 3 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210826 MGI 1317408 Lamp3 lysosomal-associated membrane protein 3 gene MP:0004781 abnormal surfactant composition IAGP N RGD:5509061 20230302 MGI PMID:34161347 1317408 Lamp3 lysosomal-associated membrane protein 3 gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20230302 MGI PMID:34161347 1317408 Lamp3 lysosomal-associated membrane protein 3 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20230302 MGI PMID:34161347 1317408 Lamp3 lysosomal-associated membrane protein 3 gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20230302 MGI PMID:34161347 1317408 Lamp3 lysosomal-associated membrane protein 3 gene MP:0010935 increased airway resistance IAGP N RGD:5509061 20230302 MGI PMID:34161347 1317408 Lamp3 lysosomal-associated membrane protein 3 gene MP:0010992 increased surfactant secretion IAGP N RGD:5509061 20230302 MGI PMID:34161347 1317409 Bltp2 bridge-like lipid transfer protein family member 2 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 1317409 Bltp2 bridge-like lipid transfer protein family member 2 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20230601 MGI 1317409 Bltp2 bridge-like lipid transfer protein family member 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1317409 Bltp2 bridge-like lipid transfer protein family member 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1317409 Bltp2 bridge-like lipid transfer protein family member 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1317409 Bltp2 bridge-like lipid transfer protein family member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1317409 Bltp2 bridge-like lipid transfer protein family member 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20230601 MGI 1317410 Paip2b poly(A) binding protein interacting protein 2B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20739757 1317410 Paip2b poly(A) binding protein interacting protein 2B gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20739757 1317410 Paip2b poly(A) binding protein interacting protein 2B gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20739757 1317410 Paip2b poly(A) binding protein interacting protein 2B gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:20739757 1317410 Paip2b poly(A) binding protein interacting protein 2B gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:20739757 1317410 Paip2b poly(A) binding protein interacting protein 2B gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:20739757 1317410 Paip2b poly(A) binding protein interacting protein 2B gene MP:0004962 decreased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:20739757 1317410 Paip2b poly(A) binding protein interacting protein 2B gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:20739757 1317410 Paip2b poly(A) binding protein interacting protein 2B gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20739757 1317410 Paip2b poly(A) binding protein interacting protein 2B gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:20739757 1317410 Paip2b poly(A) binding protein interacting protein 2B gene MP:0009231 detached acrosome IAGP N RGD:5509061 20141003 MGI PMID:20739757 1317410 Paip2b poly(A) binding protein interacting protein 2B gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:20739757 1317410 Paip2b poly(A) binding protein interacting protein 2B gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20141003 MGI PMID:20739757 1317412 Pcnt pericentrin (kendrin) gene MP:0000111 cleft palate IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0000433 microcephaly IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:15314648 1317412 Pcnt pericentrin (kendrin) gene MP:0000562 polydactyly IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0000564 syndactyly IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:20096683 1317412 Pcnt pericentrin (kendrin) gene MP:0000774 decreased brain size IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15314648 1317412 Pcnt pericentrin (kendrin) gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:15314648 1317412 Pcnt pericentrin (kendrin) gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1317412 Pcnt pericentrin (kendrin) gene MP:0001147 small testis IEA N RGD:5509061 20230119 MGI 1317412 Pcnt pericentrin (kendrin) gene MP:0001177 atelectasis IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0001258 decreased body length IEA N RGD:5509061 20230119 MGI 1317412 Pcnt pericentrin (kendrin) gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 1317412 Pcnt pericentrin (kendrin) gene MP:0001293 anophthalmia IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0001297 microphthalmia IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1317412 Pcnt pericentrin (kendrin) gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1317412 Pcnt pericentrin (kendrin) gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15314648 1317412 Pcnt pericentrin (kendrin) gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20096683 1317412 Pcnt pericentrin (kendrin) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15314648 1317412 Pcnt pericentrin (kendrin) gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1317412 Pcnt pericentrin (kendrin) gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:20096683 1317412 Pcnt pericentrin (kendrin) gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 1317412 Pcnt pericentrin (kendrin) gene MP:0003675 kidney cyst IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20096683 1317412 Pcnt pericentrin (kendrin) gene MP:0004017 duplex kidney IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:20096683 1317412 Pcnt pericentrin (kendrin) gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:20096683 1317412 Pcnt pericentrin (kendrin) gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20096683 1317412 Pcnt pericentrin (kendrin) gene MP:0006045 mitral valve regurgitation IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:20096683 1317412 Pcnt pericentrin (kendrin) gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:20096683 1317412 Pcnt pericentrin (kendrin) gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1317412 Pcnt pericentrin (kendrin) gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317412 Pcnt pericentrin (kendrin) gene MP:0012285 misaligned sternebrae IAGP N RGD:5509061 20160211 MGI PMID:25220058 1317414 Cldn4 claudin 4 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:23284964 1317414 Cldn4 claudin 4 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:23284964 1317414 Cldn4 claudin 4 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:23284964 1317414 Cldn4 claudin 4 gene MP:0000535 ureter urothelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23284964 1317414 Cldn4 claudin 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150122 MGI PMID:25157135 1317414 Cldn4 claudin 4 gene MP:0001762 polyuria IAGP N RGD:5509061 20150122 MGI PMID:25157135 1317414 Cldn4 claudin 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23284964 1317414 Cldn4 claudin 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150129 MGI PMID:25106430 1317414 Cldn4 claudin 4 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20150122 MGI PMID:25157135 1317414 Cldn4 claudin 4 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20150122 MGI PMID:25157135 1317414 Cldn4 claudin 4 gene MP:0003016 increased circulating bicarbonate level IAGP N RGD:5509061 20150122 MGI PMID:25157135 1317414 Cldn4 claudin 4 gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20150122 MGI PMID:25157135 1317414 Cldn4 claudin 4 gene MP:0003028 alkalosis IAGP N RGD:5509061 20150122 MGI PMID:25157135 1317414 Cldn4 claudin 4 gene MP:0003589 abnormal ureter physiology IAGP N RGD:5509061 20141003 MGI PMID:23284964 1317414 Cldn4 claudin 4 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20150122 MGI PMID:25157135 1317414 Cldn4 claudin 4 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:23284964 1317414 Cldn4 claudin 4 gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20150122 MGI PMID:25157135 1317414 Cldn4 claudin 4 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20150122 MGI PMID:25157135 1317414 Cldn4 claudin 4 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:23284964 1317414 Cldn4 claudin 4 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20150122 MGI PMID:25157135 1317414 Cldn4 claudin 4 gene MP:0010109 abnormal renal sodium reabsorption IAGP N RGD:5509061 20150122 MGI PMID:25157135 1317414 Cldn4 claudin 4 gene MP:0010111 abnormal renal calcium reabsorption IAGP N RGD:5509061 20141003 MGI PMID:23284964 1317414 Cldn4 claudin 4 gene MP:0011336 abnormal kidney pelvis urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23284964 1317414 Cldn4 claudin 4 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23284964 1317414 Cldn4 claudin 4 gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:23284964 1317414 Cldn4 claudin 4 gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20150122 MGI PMID:25157135 1317418 R3hcc1l R3H domain and coiled-coil containing 1 like gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20181227 MGI 1317418 R3hcc1l R3H domain and coiled-coil containing 1 like gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1317418 R3hcc1l R3H domain and coiled-coil containing 1 like gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15798182 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:15798182 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:15798182 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15798182 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15923606 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:15798182 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:15798182 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:15798182 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:15798182 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:15798182 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0010017 visceral vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15798182 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15798182 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15798182 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0010020 spleen vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15798182 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15798182 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15923606 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15923606 1317424 Morf4l1 mortality factor 4 like 1 gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:15798182 1317428 Cemip2 cell migration inducing hyaluronidase 2 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20240404 MGI PMID:34624311 1317428 Cemip2 cell migration inducing hyaluronidase 2 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20240404 MGI PMID:34624311 1317428 Cemip2 cell migration inducing hyaluronidase 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20240404 MGI PMID:34624311 1317428 Cemip2 cell migration inducing hyaluronidase 2 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20240404 MGI PMID:34624311 1317428 Cemip2 cell migration inducing hyaluronidase 2 gene MP:0002827 abnormal renal corpuscle morphology IAGP N RGD:5509061 20240404 MGI PMID:34624311 1317428 Cemip2 cell migration inducing hyaluronidase 2 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20240404 MGI PMID:34624311 1317428 Cemip2 cell migration inducing hyaluronidase 2 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20240404 MGI PMID:34624311 1317428 Cemip2 cell migration inducing hyaluronidase 2 gene MP:0014427 increased circulating hyaluronic acid level IAGP N RGD:5509061 20240425 MGI PMID:34624311 1317428 Cemip2 cell migration inducing hyaluronidase 2 gene MP:0014429 increased hyaluronic acid level IAGP N RGD:5509061 20240425 MGI PMID:34624311 1317430 Mrpl58 mitochondrial ribosomal protein L58 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220811 MGI 1317430 Mrpl58 mitochondrial ribosomal protein L58 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1317430 Mrpl58 mitochondrial ribosomal protein L58 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1317430 Mrpl58 mitochondrial ribosomal protein L58 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1317430 Mrpl58 mitochondrial ribosomal protein L58 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0000256 echinocytosis IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317433 Ppp1r15b protein phosphatase 1, regulatory subunit 15B gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19181853 1317435 Def6 differentially expressed in FDCP 6 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16470246 1317435 Def6 differentially expressed in FDCP 6 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16470246 1317435 Def6 differentially expressed in FDCP 6 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:16470246 1317435 Def6 differentially expressed in FDCP 6 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16470246 1317435 Def6 differentially expressed in FDCP 6 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16470246 1317435 Def6 differentially expressed in FDCP 6 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16470246 1317435 Def6 differentially expressed in FDCP 6 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:16470246 1317435 Def6 differentially expressed in FDCP 6 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16470246 1317435 Def6 differentially expressed in FDCP 6 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16470246 1317435 Def6 differentially expressed in FDCP 6 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16470246 1317435 Def6 differentially expressed in FDCP 6 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16470246 1317437 Car14 carbonic anhydrase 14 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16260723 1317437 Car14 carbonic anhydrase 14 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1317437 Car14 carbonic anhydrase 14 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16260723 1317437 Car14 carbonic anhydrase 14 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16260723 1317437 Car14 carbonic anhydrase 14 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16260723 1317437 Car14 carbonic anhydrase 14 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1317437 Car14 carbonic anhydrase 14 gene MP:0004043 abnormal pH regulation IAGP N RGD:5509061 20141003 MGI PMID:16260723 1317437 Car14 carbonic anhydrase 14 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1317437 Car14 carbonic anhydrase 14 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20210128 MGI 1317437 Car14 carbonic anhydrase 14 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20190502 MGI 1317442 Usp30 ubiquitin specific peptidase 30 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1317442 Usp30 ubiquitin specific peptidase 30 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1317442 Usp30 ubiquitin specific peptidase 30 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210520 MGI 1317442 Usp30 ubiquitin specific peptidase 30 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20200423 MGI PMID:32142684 1317442 Usp30 ubiquitin specific peptidase 30 gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20200423 MGI PMID:32142684 1317444 Glrx2 glutaredoxin 2 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:21983434 1317444 Glrx2 glutaredoxin 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:21983434 1317448 Tmem104 transmembrane protein 104 gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 1317448 Tmem104 transmembrane protein 104 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1317448 Tmem104 transmembrane protein 104 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1317448 Tmem104 transmembrane protein 104 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1317449 Prr5 proline rich 5 (renal) gene MP:0001513 limb grasping IEA N RGD:5509061 20220811 MGI 1317449 Prr5 proline rich 5 (renal) gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1317449 Prr5 proline rich 5 (renal) gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220811 MGI 1317449 Prr5 proline rich 5 (renal) gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1317449 Prr5 proline rich 5 (renal) gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1317454 Actr5 ARP5 actin-related protein 5 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1317454 Actr5 ARP5 actin-related protein 5 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1317454 Actr5 ARP5 actin-related protein 5 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20181227 MGI 1317454 Actr5 ARP5 actin-related protein 5 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20181227 MGI 1317454 Actr5 ARP5 actin-related protein 5 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20181227 MGI 1317454 Actr5 ARP5 actin-related protein 5 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1317454 Actr5 ARP5 actin-related protein 5 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20181227 MGI 1317454 Actr5 ARP5 actin-related protein 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317454 Actr5 ARP5 actin-related protein 5 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1317465 Ppa2 pyrophosphatase (inorganic) 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1317465 Ppa2 pyrophosphatase (inorganic) 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210520 MGI 1317468 Phyhipl phytanoyl-CoA hydroxylase interacting protein-like gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20240314 MGI PMID:33712038 1317468 Phyhipl phytanoyl-CoA hydroxylase interacting protein-like gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20240314 MGI PMID:33712038 1317468 Phyhipl phytanoyl-CoA hydroxylase interacting protein-like gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20240314 MGI PMID:33712038 1317468 Phyhipl phytanoyl-CoA hydroxylase interacting protein-like gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20240314 MGI PMID:33712038 1317468 Phyhipl phytanoyl-CoA hydroxylase interacting protein-like gene MP:0001405 impaired coordination IAGP N RGD:5509061 20240314 MGI PMID:33712038 1317468 Phyhipl phytanoyl-CoA hydroxylase interacting protein-like gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20240314 MGI PMID:33712038 1317468 Phyhipl phytanoyl-CoA hydroxylase interacting protein-like gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20240314 MGI PMID:33712038 1317468 Phyhipl phytanoyl-CoA hydroxylase interacting protein-like gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20240314 MGI PMID:33712038 1317468 Phyhipl phytanoyl-CoA hydroxylase interacting protein-like gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240314 MGI PMID:33712038 1317471 Sync syncoilin gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:18367591 1317471 Sync syncoilin gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18594912 1317471 Sync syncoilin gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:18594912 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11927621 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10601352 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11927621 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:17142777 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17142777 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:17142777 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:11927621 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10601352 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11927621 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11927621 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:18550846 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10601352 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:17142777 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:12869507 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:10601352 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:11927621 1317473 Selplg selectin, platelet (p-selectin) ligand gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:18550846 1317475 Rilpl1 Rab interacting lysosomal protein-like 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1317475 Rilpl1 Rab interacting lysosomal protein-like 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 1317477 Pkd1l3 polycystic kidney disease 1 like 3 gene MP:0001985 abnormal gustatory system physiology IAGP N RGD:5509061 20141003 MGI PMID:21625513 1317477 Pkd1l3 polycystic kidney disease 1 like 3 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:21625513 1317487 Luc7l3 LUC7-like 3 (S. cerevisiae) gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1317487 Luc7l3 LUC7-like 3 (S. cerevisiae) gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1317487 Luc7l3 LUC7-like 3 (S. cerevisiae) gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1317487 Luc7l3 LUC7-like 3 (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1317487 Luc7l3 LUC7-like 3 (S. cerevisiae) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1317488 Ola1 Obg-like ATPase 1 gene MP:0000597 delayed hepatic development IAGP N RGD:5509061 20170608 MGI PMID:27481995 1317488 Ola1 Obg-like ATPase 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20170608 MGI PMID:27481995 1317488 Ola1 Obg-like ATPase 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20170608 MGI PMID:27481995 1317488 Ola1 Obg-like ATPase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170608 MGI PMID:27481995 1317488 Ola1 Obg-like ATPase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170608 MGI PMID:27481995 1317488 Ola1 Obg-like ATPase 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20170608 MGI PMID:27481995 1317488 Ola1 Obg-like ATPase 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1317488 Ola1 Obg-like ATPase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170608 MGI PMID:27481995 1317488 Ola1 Obg-like ATPase 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20170608 MGI PMID:27481995 1317488 Ola1 Obg-like ATPase 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20170608 MGI PMID:27481995 1317488 Ola1 Obg-like ATPase 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20170608 MGI PMID:27481995 1317488 Ola1 Obg-like ATPase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20170608 MGI PMID:27481995 1317488 Ola1 Obg-like ATPase 1 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20201022 MGI 1317488 Ola1 Obg-like ATPase 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20170608 MGI PMID:27481995 1317488 Ola1 Obg-like ATPase 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20170608 MGI PMID:27481995 1317488 Ola1 Obg-like ATPase 1 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20170608 MGI PMID:27481995 1317488 Ola1 Obg-like ATPase 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20170608 MGI PMID:27481995 1317488 Ola1 Obg-like ATPase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317495 Pnpt1 polyribonucleotide nucleotidyltransferase 1 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20160804 MGI 1317495 Pnpt1 polyribonucleotide nucleotidyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20691904 1317495 Pnpt1 polyribonucleotide nucleotidyltransferase 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1317495 Pnpt1 polyribonucleotide nucleotidyltransferase 1 gene MP:0005298 abnormal clavicle morphology IEA N RGD:5509061 20160804 MGI 1317495 Pnpt1 polyribonucleotide nucleotidyltransferase 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1317495 Pnpt1 polyribonucleotide nucleotidyltransferase 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:20691904 1317495 Pnpt1 polyribonucleotide nucleotidyltransferase 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:20691904 1317495 Pnpt1 polyribonucleotide nucleotidyltransferase 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:20691904 1317495 Pnpt1 polyribonucleotide nucleotidyltransferase 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:20691904 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0000745 tremors IEA N RGD:5509061 20111116 MGI 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20190418 MGI PMID:27528230 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190418 MGI PMID:27528230 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0001923 reduced female fertility IEA N RGD:5509061 20111116 MGI 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0001926 female infertility IEA N RGD:5509061 20111116 MGI 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0002680 decreased corpora lutea number IEA N RGD:5509061 20111116 MGI 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0002687 oligozoospermia IEA N RGD:5509061 20111116 MGI 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20160929 MGI PMID:27534441 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0004901 decreased male germ cell number IEA N RGD:5509061 20111116 MGI 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20111116 MGI 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20190418 MGI PMID:27528230 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0006380 abnormal spermatid morphology IEA N RGD:5509061 20111116 MGI 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20190418 MGI PMID:27528230 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20190418 MGI PMID:27528230 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20190418 MGI PMID:27528230 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0013159 Purkinje cell axonal dystrophy IAGP N RGD:5509061 20190418 MGI PMID:27528230 1317499 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20160929 MGI PMID:27534441 1317501 Cytip cytohesin 1 interacting protein gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16809763 1317501 Cytip cytohesin 1 interacting protein gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16809763 1317501 Cytip cytohesin 1 interacting protein gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16809763 1317501 Cytip cytohesin 1 interacting protein gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:16809763 1317501 Cytip cytohesin 1 interacting protein gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16809763 1317501 Cytip cytohesin 1 interacting protein gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:16914744 1317501 Cytip cytohesin 1 interacting protein gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16809763 1317501 Cytip cytohesin 1 interacting protein gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:16809763 1317503 Sh2d4a SH2 domain containing 4A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18641339 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0002080 prenatal lethality IEA N RGD:5509061 20201231 MGI 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191128 MGI 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0003087 absent allantois IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0009331 absent primitive node IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0012724 absent head fold IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191128 MGI 1317512 Mrps18c mitochondrial ribosomal protein S18C gene MP:0014246 decreased cellular ATP level IAGP N RGD:5509061 20241024 MGI PMID:32376682 1317515 Plagl2 pleiomorphic adenoma gene-like 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:17983586 1317515 Plagl2 pleiomorphic adenoma gene-like 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17983586 1317515 Plagl2 pleiomorphic adenoma gene-like 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17983586 1317515 Plagl2 pleiomorphic adenoma gene-like 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17983586 1317515 Plagl2 pleiomorphic adenoma gene-like 2 gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:17983586 1317515 Plagl2 pleiomorphic adenoma gene-like 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17983586 1317515 Plagl2 pleiomorphic adenoma gene-like 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17983586 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20210930 MGI PMID:33905568 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20181227 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20181227 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000458 abnormal mandible morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000552 abnormal radius morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0001340 abnormal eyelid morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0002187 abnormal fibula morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0004692 small pubis IAGP N RGD:5509061 20210930 MGI PMID:33905568 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20181227 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0005108 abnormal ulna morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0005270 abnormal zygomatic bone morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0005298 abnormal clavicle morphology IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20210128 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20211021 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20210128 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20160421 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20141003 MGI 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0012072 decreased susceptibility to osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:23526378 1317517 Lrrk1 leucine-rich repeat kinase 1 gene MP:0030610 absent teeth IEA N RGD:5509061 20180726 MGI 1317519 Med16 mediator complex subunit 16 gene MP:0000603 pale liver IEA N RGD:5509061 20210520 MGI 1317519 Med16 mediator complex subunit 16 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20170504 MGI 1317519 Med16 mediator complex subunit 16 gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1317519 Med16 mediator complex subunit 16 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1317519 Med16 mediator complex subunit 16 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20170504 MGI 1317519 Med16 mediator complex subunit 16 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317523 Farp2 FERM, RhoGEF and pleckstrin domain protein 2 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20190124 MGI PMID:25340873 1317523 Farp2 FERM, RhoGEF and pleckstrin domain protein 2 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:20702777 1317523 Farp2 FERM, RhoGEF and pleckstrin domain protein 2 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1317523 Farp2 FERM, RhoGEF and pleckstrin domain protein 2 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:20702777 1317523 Farp2 FERM, RhoGEF and pleckstrin domain protein 2 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:20702777 1317523 Farp2 FERM, RhoGEF and pleckstrin domain protein 2 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:20702777 1317523 Farp2 FERM, RhoGEF and pleckstrin domain protein 2 gene MP:0008861 abnormal hair shedding IAGP N RGD:5509061 20190124 MGI PMID:25340873 1317523 Farp2 FERM, RhoGEF and pleckstrin domain protein 2 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:20702777 1317523 Farp2 FERM, RhoGEF and pleckstrin domain protein 2 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:20702777 1317523 Farp2 FERM, RhoGEF and pleckstrin domain protein 2 gene MP:0010877 abnormal trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:20702777 1317525 Shpk sedoheptulokinase gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20240822 MGI PMID:34823997 1317525 Shpk sedoheptulokinase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20240822 MGI PMID:34823997 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:22044588 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:22044588 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:23726973 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22044588 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23726973 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22044588 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23726973 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22044588 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:22044588 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:22044588 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0008402 increased cellular sensitivity to alkylating agents IAGP N RGD:5509061 20141003 MGI PMID:23726973 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:23726973 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23726973 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23726973 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23726973 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0010156 abnormal small intestinal crypt cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23726973 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23726973 1317527 Tigar Trp53 induced glycolysis regulatory phosphatase gene MP:0011638 abnormal mitochondrial chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:22044588 1317529 Ccr1l1 C-C motif chemokine receptor 1 like 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1317529 Ccr1l1 C-C motif chemokine receptor 1 like 1 gene MP:0005387 immune system phenotype IAGP N RGD:5509061 20210617 MGI PMID:33548230 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20201022 MGI 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20160421 MGI 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20170518 MGI PMID:27777970 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0003173 decreased lysosomal enzyme secretion IAGP N RGD:5509061 20170518 MGI PMID:27777970 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20170518 MGI PMID:27777970 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20170518 MGI PMID:27777970 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20170518 MGI PMID:27777970 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20170518 MGI PMID:27777970 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20181227 MGI 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20160811 MGI 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20160421 MGI 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20160421 MGI 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20170518 MGI PMID:27777970 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20170518 MGI PMID:27777970 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20170518 MGI PMID:27777970 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20170518 MGI PMID:27777970 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20170518 MGI PMID:27777970 1317533 Plekhm1 pleckstrin homology domain containing, family M (with RUN domain) member 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20170518 MGI PMID:27777970 1317535 Efhc1 EF-hand domain (C-terminal) containing 1 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:19147686 1317535 Efhc1 EF-hand domain (C-terminal) containing 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:19147686 1317535 Efhc1 EF-hand domain (C-terminal) containing 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:19147686 1317535 Efhc1 EF-hand domain (C-terminal) containing 1 gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:19147686 1317535 Efhc1 EF-hand domain (C-terminal) containing 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:19147686 1317536 Dennd6b DENN domain containing 6B gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 1317536 Dennd6b DENN domain containing 6B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1317536 Dennd6b DENN domain containing 6B gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20230119 MGI 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:12203729 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:16291793 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:12024028 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12203729 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0002251 abnormal nasopharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:12203729 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:12203729 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0003760 decreased palatal length IAGP N RGD:5509061 20141003 MGI PMID:12203729 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:12203729 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:16291793 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:12024028 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:12203729 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12203729 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:12203729 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20141003 MGI PMID:12203729 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0010994 aerophagia IAGP N RGD:5509061 20141003 MGI PMID:12203729 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12203729 1317541 Sim2 single-minded family bHLH transcription factor 2 gene MP:0014429 increased hyaluronic acid level IAGP N RGD:5509061 20240425 MGI PMID:12203729 1317543 Rbm7 RNA binding motif protein 7 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20201001 MGI PMID:32187520 1317543 Rbm7 RNA binding motif protein 7 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20201001 MGI PMID:32187520 1317543 Rbm7 RNA binding motif protein 7 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20201001 MGI PMID:32187520 1317543 Rbm7 RNA binding motif protein 7 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20201001 MGI PMID:32187520 1317543 Rbm7 RNA binding motif protein 7 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20201001 MGI PMID:32187520 1317545 Ccnk cyclin K gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22012619 1317549 Cpne5 copine V gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20160811 MGI 1317549 Cpne5 copine V gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20230126 MGI PMID:28168849 1317551 Ppp2r5a protein phosphatase 2, regulatory subunit B', alpha gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20181004 MGI PMID:29190822 1317551 Ppp2r5a protein phosphatase 2, regulatory subunit B', alpha gene MP:0000414 alopecia IAGP N RGD:5509061 20181004 MGI PMID:29190822 1317551 Ppp2r5a protein phosphatase 2, regulatory subunit B', alpha gene MP:0000599 enlarged liver IAGP N RGD:5509061 20181004 MGI PMID:29190822 1317551 Ppp2r5a protein phosphatase 2, regulatory subunit B', alpha gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20181004 MGI PMID:29190822 1317551 Ppp2r5a protein phosphatase 2, regulatory subunit B', alpha gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1317551 Ppp2r5a protein phosphatase 2, regulatory subunit B', alpha gene MP:0001212 skin lesions IAGP N RGD:5509061 20181004 MGI PMID:29190822 1317551 Ppp2r5a protein phosphatase 2, regulatory subunit B', alpha gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20181004 MGI PMID:29190822 1317551 Ppp2r5a protein phosphatase 2, regulatory subunit B', alpha gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1317551 Ppp2r5a protein phosphatase 2, regulatory subunit B', alpha gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20181004 MGI PMID:29190822 1317551 Ppp2r5a protein phosphatase 2, regulatory subunit B', alpha gene MP:0004971 dermal hyperplasia IAGP N RGD:5509061 20181004 MGI PMID:29190822 1317551 Ppp2r5a protein phosphatase 2, regulatory subunit B', alpha gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20181004 MGI PMID:29190822 1317551 Ppp2r5a protein phosphatase 2, regulatory subunit B', alpha gene MP:0009794 sebaceous gland hyperplasia IAGP N RGD:5509061 20181004 MGI PMID:29190822 1317551 Ppp2r5a protein phosphatase 2, regulatory subunit B', alpha gene MP:0012110 increased hair follicle number IAGP N RGD:5509061 20181004 MGI PMID:29190822 1317552 Ralgapa2 Ral GTPase activating protein, alpha subunit 2 (catalytic) gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22450745 1317552 Ralgapa2 Ral GTPase activating protein, alpha subunit 2 (catalytic) gene MP:0010289 increased urinary system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22450745 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20240523 MGI 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0001147 small testis IEA N RGD:5509061 20240523 MGI 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20231123 MGI PMID:37891173 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0013507 increased ovary apoptosis IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20190502 MGI PMID:30305635 1317557 Swsap1 SWIM type zinc finger 7 associated protein 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20240523 MGI 1317559 Cldn10 claudin 10 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0006357 abnormal circulating mineral level IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0010092 increased circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0010111 abnormal renal calcium reabsorption IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0011436 decreased urine magnesium level IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317559 Cldn10 claudin 10 gene MP:0011467 decreased urine urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:22891322 1317561 Pdgfrl platelet-derived growth factor receptor-like gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1317561 Pdgfrl platelet-derived growth factor receptor-like gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210520 MGI 1317563 Eif5a eukaryotic translation initiation factor 5A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200521 MGI PMID:21850436 1317563 Eif5a eukaryotic translation initiation factor 5A gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20200521 MGI PMID:21850436 1317563 Eif5a eukaryotic translation initiation factor 5A gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200521 MGI PMID:21850436 1317564 Glis1 GLIS family zinc finger 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:12385751 1317564 Glis1 GLIS family zinc finger 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12385751 1317564 Glis1 GLIS family zinc finger 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12385751 1317565 Ccdc159 coiled-coil domain containing 159 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20240808 MGI PMID:38236177 1317565 Ccdc159 coiled-coil domain containing 159 gene MP:0001925 male infertility IAGP N RGD:5509061 20240808 MGI PMID:38236177 1317565 Ccdc159 coiled-coil domain containing 159 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20240808 MGI PMID:38236177 1317565 Ccdc159 coiled-coil domain containing 159 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20240808 MGI PMID:38236177 1317565 Ccdc159 coiled-coil domain containing 159 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20240808 MGI PMID:38236177 1317565 Ccdc159 coiled-coil domain containing 159 gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20240808 MGI PMID:38236177 1317565 Ccdc159 coiled-coil domain containing 159 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20240808 MGI PMID:38236177 1317565 Ccdc159 coiled-coil domain containing 159 gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20240808 MGI PMID:38236177 1317565 Ccdc159 coiled-coil domain containing 159 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20240808 MGI PMID:38236177 1317565 Ccdc159 coiled-coil domain containing 159 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20240808 MGI PMID:38236177 1317565 Ccdc159 coiled-coil domain containing 159 gene MP:0014468 disorganized sperm mitochondrial sheath IAGP N RGD:5509061 20240808 MGI PMID:38236177 1317565 Ccdc159 coiled-coil domain containing 159 gene MP:0030591 absent sperm fibrous sheath IAGP N RGD:5509061 20240808 MGI PMID:38236177 1317570 Ankrd6 ankyrin repeat domain 6 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20150924 MGI PMID:25218921 1317570 Ankrd6 ankyrin repeat domain 6 gene MP:0001926 female infertility IAGP N RGD:5509061 20150924 MGI PMID:25218921 1317570 Ankrd6 ankyrin repeat domain 6 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20150924 MGI PMID:25218921 1317570 Ankrd6 ankyrin repeat domain 6 gene MP:0002623 abnormal vestibular hair cell morphology IAGP N RGD:5509061 20151001 MGI PMID:25218921 1317570 Ankrd6 ankyrin repeat domain 6 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20150924 MGI PMID:25218921 1317572 Rnf8 ring finger protein 8 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317572 Rnf8 ring finger protein 8 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20385750 1317574 Setd1b SET domain containing 1B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24550110 1317574 Setd1b SET domain containing 1B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24550110 1317576 Vps11 VPS11, CORVET/HOPS core subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12578828 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12578828 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12578828 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:12578828 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12578828 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0001805 decreased IgG level IEA N RGD:5509061 20180215 MGI 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12578828 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12578828 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12578828 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0002491 decreased IgD level IEA N RGD:5509061 20180215 MGI 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:23657012 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:12578828 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:12578828 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:23254285 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:23333305 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20170615 MGI PMID:26774285 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:20368578 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:23254285 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20170615 MGI PMID:26774285 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20210826 MGI PMID:33857404 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20180215 MGI 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12578828 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23254285 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:23333305 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12578828 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0008409 increased cellular sensitivity to hydroxyurea IAGP N RGD:5509061 20141003 MGI PMID:23254285 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:23254285 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:12578828 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20210826 MGI PMID:33857404 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20170615 MGI PMID:26774285 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12640136 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1317578 Trp53bp1 transformation related protein 53 binding protein 1 gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20180215 MGI 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:17021036 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10624948 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11511537 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17021036 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17828260 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0000860 abnormal primary somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17828260 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0000862 absent barrels in primary somatosensory cortex IAGP N RGD:5509061 20141003 MGI PMID:10624948 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9271116 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220127 MGI PMID:31600777 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:20147377 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:20147377 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0001437 no swallowing reflex IAGP N RGD:5509061 20141003 MGI PMID:9271116 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20220127 MGI PMID:31600777 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20220127 MGI PMID:31600777 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20220127 MGI PMID:31600777 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20220127 MGI PMID:31600777 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20220127 MGI PMID:31600777 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:10624948 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17828260 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:17021036 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20181220 MGI PMID:30217595 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17021036 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:17021036 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:9271116 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16914494 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0003989 abnormal barrel cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17828260 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20220127 MGI PMID:31600777 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004144 hypotonia IAGP N RGD:5509061 20220127 MGI PMID:31600777 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004167 abnormal cingulate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:17021036 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:20147377 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004330 abnormal vestibular saccular macula morphology IAGP N RGD:5509061 20181220 MGI PMID:30217595 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20181220 MGI PMID:30217595 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20181220 MGI PMID:30217595 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16914494 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20181220 MGI PMID:30217595 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16914494 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004407 increased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16914494 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16914494 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16914494 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004589 abnormal cochlear hair cell development IAGP N RGD:5509061 20141003 MGI PMID:16914494 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0004840 increased Deiters cell number IAGP N RGD:5509061 20141003 MGI PMID:16914494 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20147377 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:20147377 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:17021036 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20181220 MGI PMID:30217595 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20220127 MGI PMID:31600777 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0008221 abnormal hippocampal commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:17021036 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:17021036 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0008304 abnormal organ of Corti supporting cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16914494 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0008307 short scala media IAGP N RGD:5509061 20141003 MGI PMID:16914494 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0008307 short scala media IAGP N RGD:5509061 20181220 MGI PMID:30217595 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20220127 MGI PMID:31600777 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9271116 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17021036 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0011389 absent optic disk IAGP N RGD:5509061 20141003 MGI PMID:20147377 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20181220 MGI PMID:30217595 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20220127 MGI PMID:31600777 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0012318 slow extinction of fear memory IAGP N RGD:5509061 20220127 MGI PMID:31600777 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0012535 abnormal optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:20147377 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0013911 fused vestibular saccule and utricle IAGP N RGD:5509061 20181220 MGI PMID:30217595 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0020068 increased neocortex volume IAGP N RGD:5509061 20220127 MGI PMID:31600777 1317579 Nr2f1 nuclear receptor subfamily 2, group F, member 1 gene MP:0020083 decreased hippocampus volume IAGP N RGD:5509061 20220127 MGI PMID:31600777 1317581 Tnfrsf10b tumor necrosis factor receptor superfamily, member 10b gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:15713653 1317581 Tnfrsf10b tumor necrosis factor receptor superfamily, member 10b gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18079967 1317581 Tnfrsf10b tumor necrosis factor receptor superfamily, member 10b gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:15589175 1317581 Tnfrsf10b tumor necrosis factor receptor superfamily, member 10b gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:15713653 1317581 Tnfrsf10b tumor necrosis factor receptor superfamily, member 10b gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:15589175 1317581 Tnfrsf10b tumor necrosis factor receptor superfamily, member 10b gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15589175 1317581 Tnfrsf10b tumor necrosis factor receptor superfamily, member 10b gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:15589175 1317581 Tnfrsf10b tumor necrosis factor receptor superfamily, member 10b gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:15589175 1317581 Tnfrsf10b tumor necrosis factor receptor superfamily, member 10b gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:15589175 1317581 Tnfrsf10b tumor necrosis factor receptor superfamily, member 10b gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:15589175 1317581 Tnfrsf10b tumor necrosis factor receptor superfamily, member 10b gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15713653 1317581 Tnfrsf10b tumor necrosis factor receptor superfamily, member 10b gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:15589175 1317581 Tnfrsf10b tumor necrosis factor receptor superfamily, member 10b gene MP:0031025 decreased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:15589175 1317584 Bms1 BMS1, ribosome biogenesis factor gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1317584 Bms1 BMS1, ribosome biogenesis factor gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1317584 Bms1 BMS1, ribosome biogenesis factor gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1317584 Bms1 BMS1, ribosome biogenesis factor gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20181227 MGI 1317584 Bms1 BMS1, ribosome biogenesis factor gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20211021 MGI 1317584 Bms1 BMS1, ribosome biogenesis factor gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20210128 MGI 1317584 Bms1 BMS1, ribosome biogenesis factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317586 Lhx4 LIM homeobox protein 4 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9865699 1317586 Lhx4 LIM homeobox protein 4 gene MP:0001070 abnormal abducens nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9865699 1317586 Lhx4 LIM homeobox protein 4 gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9865699 1317586 Lhx4 LIM homeobox protein 4 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9865699 1317586 Lhx4 LIM homeobox protein 4 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:7913017 1317586 Lhx4 LIM homeobox protein 4 gene MP:0002329 abnormal blood gas level IAGP N RGD:5509061 20141003 MGI PMID:7913017 1317586 Lhx4 LIM homeobox protein 4 gene MP:0003972 decreased pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:12183375 1317586 Lhx4 LIM homeobox protein 4 gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12183375 1317586 Lhx4 LIM homeobox protein 4 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:12183375 1317586 Lhx4 LIM homeobox protein 4 gene MP:0008320 absent adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:12183375 1317586 Lhx4 LIM homeobox protein 4 gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:12183375 1317586 Lhx4 LIM homeobox protein 4 gene MP:0008335 decreased gonadotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:12183375 1317586 Lhx4 LIM homeobox protein 4 gene MP:0008336 absent gonadotrophs IAGP N RGD:5509061 20141003 MGI PMID:12183375 1317586 Lhx4 LIM homeobox protein 4 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:7913017 1317586 Lhx4 LIM homeobox protein 4 gene MP:0010890 decreased alveolar lamellar body number IAGP N RGD:5509061 20141003 MGI PMID:12183375 1317586 Lhx4 LIM homeobox protein 4 gene MP:0010890 decreased alveolar lamellar body number IAGP N RGD:5509061 20141003 MGI PMID:7913017 1317586 Lhx4 LIM homeobox protein 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7913017 1317586 Lhx4 LIM homeobox protein 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9865699 1317586 Lhx4 LIM homeobox protein 4 gene MP:0013349 small Rathke's pouch IAGP N RGD:5509061 20141218 MGI PMID:12183375 1317586 Lhx4 LIM homeobox protein 4 gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:12183375 1317586 Lhx4 LIM homeobox protein 4 gene MP:0013352 abnormal Rathke's pouch apoptosis IAGP N RGD:5509061 20141218 MGI PMID:12183375 1317588 Usp12 ubiquitin specific peptidase 12 gene MP:0000565 oligodactyly IEA N RGD:5509061 20160804 MGI 1317588 Usp12 ubiquitin specific peptidase 12 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1317588 Usp12 ubiquitin specific peptidase 12 gene MP:0001807 decreased IgA level IEA N RGD:5509061 20160804 MGI 1317588 Usp12 ubiquitin specific peptidase 12 gene MP:0002833 increased heart weight IEA N RGD:5509061 20160804 MGI 1317588 Usp12 ubiquitin specific peptidase 12 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20160804 MGI 1317588 Usp12 ubiquitin specific peptidase 12 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1317588 Usp12 ubiquitin specific peptidase 12 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1317588 Usp12 ubiquitin specific peptidase 12 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1317588 Usp12 ubiquitin specific peptidase 12 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20201022 MGI 1317588 Usp12 ubiquitin specific peptidase 12 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 1317588 Usp12 ubiquitin specific peptidase 12 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20160804 MGI 1317590 Dnajc13 DnaJ heat shock protein family (Hsp40) member C13 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200507 MGI PMID:31082451 1317590 Dnajc13 DnaJ heat shock protein family (Hsp40) member C13 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1317590 Dnajc13 DnaJ heat shock protein family (Hsp40) member C13 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20231207 MGI 1317590 Dnajc13 DnaJ heat shock protein family (Hsp40) member C13 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1317590 Dnajc13 DnaJ heat shock protein family (Hsp40) member C13 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1317590 Dnajc13 DnaJ heat shock protein family (Hsp40) member C13 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1317590 Dnajc13 DnaJ heat shock protein family (Hsp40) member C13 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1317591 Gsx2 GS homeobox 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:19709628 1317591 Gsx2 GS homeobox 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:19709628 1317591 Gsx2 GS homeobox 2 gene MP:0000828 abnormal fourth ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9398437 1317591 Gsx2 GS homeobox 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:19208224 1317591 Gsx2 GS homeobox 2 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:19709628 1317591 Gsx2 GS homeobox 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9398437 1317591 Gsx2 GS homeobox 2 gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:9398437 1317591 Gsx2 GS homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19709628 1317591 Gsx2 GS homeobox 2 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:19709628 1317591 Gsx2 GS homeobox 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:9398437 1317591 Gsx2 GS homeobox 2 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:19208224 1317591 Gsx2 GS homeobox 2 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19208224 1317591 Gsx2 GS homeobox 2 gene MP:0004103 abnormal ventral striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:11731457 1317591 Gsx2 GS homeobox 2 gene MP:0004186 abnormal area postrema morphology IAGP N RGD:5509061 20141003 MGI PMID:9398437 1317591 Gsx2 GS homeobox 2 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:19208224 1317591 Gsx2 GS homeobox 2 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:19709628 1317591 Gsx2 GS homeobox 2 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:9398437 1317591 Gsx2 GS homeobox 2 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:19208224 1317591 Gsx2 GS homeobox 2 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:9398437 1317591 Gsx2 GS homeobox 2 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19208224 1317591 Gsx2 GS homeobox 2 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:9398437 1317591 Gsx2 GS homeobox 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:9398437 1317591 Gsx2 GS homeobox 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19709628 1317591 Gsx2 GS homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9398437 1317591 Gsx2 GS homeobox 2 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:11731457 1317591 Gsx2 GS homeobox 2 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:19709628 1317592 Pithd1 PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20200528 MGI PMID:31915251 1317592 Pithd1 PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200528 MGI PMID:31915251 1317592 Pithd1 PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200528 MGI PMID:31915251 1317592 Pithd1 PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20200528 MGI PMID:31915251 1317592 Pithd1 PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1 gene MP:0005379 endocrine/exocrine gland phenotype IAGP N RGD:5509061 20200528 MGI PMID:31915251 1317592 Pithd1 PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20200528 MGI PMID:31915251 1317592 Pithd1 PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20200528 MGI PMID:31915251 1317592 Pithd1 PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1 gene MP:0031408 multi-headed sperm IAGP N RGD:5509061 20220630 MGI PMID:31915251 1317595 Irf4 interferon regulatory factor 4 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210128 MGI 1317595 Irf4 interferon regulatory factor 4 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210520 MGI 1317595 Irf4 interferon regulatory factor 4 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210520 MGI 1317595 Irf4 interferon regulatory factor 4 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0001260 increased body weight IAGP N RGD:5509061 20180208 MGI PMID:24995979 1317595 Irf4 interferon regulatory factor 4 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20221215 MGI 1317595 Irf4 interferon regulatory factor 4 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12832394 1317595 Irf4 interferon regulatory factor 4 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1317595 Irf4 interferon regulatory factor 4 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12832394 1317595 Irf4 interferon regulatory factor 4 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1317595 Irf4 interferon regulatory factor 4 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12832394 1317595 Irf4 interferon regulatory factor 4 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16767092 1317595 Irf4 interferon regulatory factor 4 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0002403 abnormal pre-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12832394 1317595 Irf4 interferon regulatory factor 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12189207 1317595 Irf4 interferon regulatory factor 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12502720 1317595 Irf4 interferon regulatory factor 4 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12189207 1317595 Irf4 interferon regulatory factor 4 gene MP:0002440 abnormal memory B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16767092 1317595 Irf4 interferon regulatory factor 4 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16767092 1317595 Irf4 interferon regulatory factor 4 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12832394 1317595 Irf4 interferon regulatory factor 4 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:16767092 1317595 Irf4 interferon regulatory factor 4 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:21613984 1317595 Irf4 interferon regulatory factor 4 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22761313 1317595 Irf4 interferon regulatory factor 4 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 1317595 Irf4 interferon regulatory factor 4 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12832394 1317595 Irf4 interferon regulatory factor 4 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12832394 1317595 Irf4 interferon regulatory factor 4 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16767092 1317595 Irf4 interferon regulatory factor 4 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20180208 MGI PMID:24995979 1317595 Irf4 interferon regulatory factor 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180208 MGI PMID:24995979 1317595 Irf4 interferon regulatory factor 4 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180208 MGI PMID:24995979 1317595 Irf4 interferon regulatory factor 4 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20180208 MGI PMID:24995979 1317595 Irf4 interferon regulatory factor 4 gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:12832394 1317595 Irf4 interferon regulatory factor 4 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12189207 1317595 Irf4 interferon regulatory factor 4 gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21613984 1317595 Irf4 interferon regulatory factor 4 gene MP:0008100 absent plasma cells IAGP N RGD:5509061 20141003 MGI PMID:16767092 1317595 Irf4 interferon regulatory factor 4 gene MP:0008100 absent plasma cells IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:15728463 1317595 Irf4 interferon regulatory factor 4 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:15184678 1317595 Irf4 interferon regulatory factor 4 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:15728463 1317595 Irf4 interferon regulatory factor 4 gene MP:0008217 abnormal B cell activation IEA N RGD:5509061 20111116 MGI 1317595 Irf4 interferon regulatory factor 4 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:16767092 1317595 Irf4 interferon regulatory factor 4 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16767092 1317595 Irf4 interferon regulatory factor 4 gene MP:0008523 absent lymph node germinal center IAGP N RGD:5509061 20141003 MGI PMID:8999800 1317595 Irf4 interferon regulatory factor 4 gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20180208 MGI PMID:24995979 1317595 Irf4 interferon regulatory factor 4 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20180208 MGI PMID:24995979 1317595 Irf4 interferon regulatory factor 4 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20180208 MGI PMID:24995979 1317595 Irf4 interferon regulatory factor 4 gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20180208 MGI PMID:24995979 1317595 Irf4 interferon regulatory factor 4 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20180208 MGI PMID:24995979 1317595 Irf4 interferon regulatory factor 4 gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20180208 MGI PMID:24995979 1317595 Irf4 interferon regulatory factor 4 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180208 MGI PMID:24995979 1317595 Irf4 interferon regulatory factor 4 gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20180208 MGI PMID:24995979 1317595 Irf4 interferon regulatory factor 4 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20180208 MGI PMID:24995979 1317595 Irf4 interferon regulatory factor 4 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20180208 MGI PMID:24995979 1317595 Irf4 interferon regulatory factor 4 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:8999800 1317601 Poll polymerase (DNA directed), lambda gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16860755 1317601 Poll polymerase (DNA directed), lambda gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16860755 1317601 Poll polymerase (DNA directed), lambda gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:16860755 1317601 Poll polymerase (DNA directed), lambda gene MP:0008761 abnormal immunoglobulin light chain V-J recombination IAGP N RGD:5509061 20141003 MGI PMID:16860755 1317601 Poll polymerase (DNA directed), lambda gene MP:0009796 abnormal base-excision repair IAGP N RGD:5509061 20141003 MGI PMID:15749700 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20160804 MGI 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:17641034 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22761313 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0005017 decreased B cell number IEA N RGD:5509061 20160804 MGI 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22761313 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17641034 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:22761313 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:16413922 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16413922 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17641034 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:16413922 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:16413922 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17641034 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:16413922 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16413922 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22761313 1317603 Nfkbid nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, delta gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17641034 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20210128 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20201022 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0002989 small kidney IEA N RGD:5509061 20201022 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20210520 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20210520 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 1317605 Neurl4 neuralized E3 ubiquitin protein ligase 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:16410414 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:23095888 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:21559415 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:11335109 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23095888 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000344 absent Cajal-Retzius cell IAGP N RGD:5509061 20141003 MGI PMID:16410414 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:21559415 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:11029008 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:9811581 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16410414 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16410414 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:8299937 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:8299937 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:16410414 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:14832454 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:8299937 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:8299937 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:21559415 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:8299937 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0001756 abnormal urination IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:14832454 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16410414 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20111116 MGI 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20111116 MGI 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0002632 vestigial tail IAGP N RGD:5509061 20141003 MGI PMID:11029008 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0002632 vestigial tail IAGP N RGD:5509061 20141003 MGI PMID:14832454 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0002632 vestigial tail IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0002861 abnormal tail bud morphology IEA N RGD:5509061 20141003 MGI 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11335109 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:8299937 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0003445 sirenomelia IAGP N RGD:5509061 20141003 MGI PMID:11335109 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0003445 sirenomelia IAGP N RGD:5509061 20141003 MGI PMID:21559415 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:21559415 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:8299937 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:8299937 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:21559415 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:8299937 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004205 absent hyoid bone IAGP N RGD:5509061 20141003 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20141003 MGI PMID:9811581 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004459 small alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:11335109 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11335109 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11335109 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11335109 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11335109 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004648 decreased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004656 absent sacral vertebrae IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0004714 truncated notochord IAGP N RGD:5509061 20141003 MGI PMID:8299937 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:8299937 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0006288 small otic capsule IAGP N RGD:5509061 20141003 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0008031 decreased Cajal-Retzius cell number IAGP N RGD:5509061 20141003 MGI PMID:16410414 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0008031 decreased Cajal-Retzius cell number IAGP N RGD:5509061 20141003 MGI PMID:19805388 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:8595882 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0008787 abnormal tailgut morphology IEA N RGD:5509061 20141003 MGI 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:16410414 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20181122 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0009845 abnormal neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23095888 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8299937 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11335109 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0012063 absent tail bud IAGP N RGD:5509061 20141003 MGI PMID:8299937 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0012714 decreased ventral ectodermal ridge size IEA N RGD:5509061 20141003 MGI 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20171005 MGI PMID:9353119 1317607 Wnt3a wingless-type MMTV integration site family, member 3A gene MP:0030383 small presphenoid bone IAGP N RGD:5509061 20171207 MGI PMID:9353119 1317609 Vezf1 vascular endothelial zinc finger 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15882861 1317609 Vezf1 vascular endothelial zinc finger 1 gene MP:0000265 blood vessel atresia IAGP N RGD:5509061 20141003 MGI PMID:15882861 1317609 Vezf1 vascular endothelial zinc finger 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15882861 1317609 Vezf1 vascular endothelial zinc finger 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15882861 1317609 Vezf1 vascular endothelial zinc finger 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15882861 1317609 Vezf1 vascular endothelial zinc finger 1 gene MP:0001699 increased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15882861 1317609 Vezf1 vascular endothelial zinc finger 1 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15882861 1317609 Vezf1 vascular endothelial zinc finger 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15882861 1317609 Vezf1 vascular endothelial zinc finger 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15882861 1317609 Vezf1 vascular endothelial zinc finger 1 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:15882861 1317609 Vezf1 vascular endothelial zinc finger 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15882861 1317609 Vezf1 vascular endothelial zinc finger 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15882861 1317609 Vezf1 vascular endothelial zinc finger 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15882861 1317609 Vezf1 vascular endothelial zinc finger 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15882861 1317609 Vezf1 vascular endothelial zinc finger 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15882861 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:18252746 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:9744877 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20220519 MGI PMID:28797108 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20220519 MGI PMID:28797108 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:21890494 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20220519 MGI PMID:28797108 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12620894 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18252745 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21890494 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0003199 calcified muscle IAGP N RGD:5509061 20141003 MGI PMID:18252746 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0003199 calcified muscle IAGP N RGD:5509061 20141003 MGI PMID:9744877 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0003397 increased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:18252746 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21890494 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18252746 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9744877 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:18252746 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:9744877 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21890494 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:21890494 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20220519 MGI PMID:28797108 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18252746 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9744877 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:9744877 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20220519 MGI PMID:28797108 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0009423 increased extensor digitorum longus weight IAGP N RGD:5509061 20141003 MGI PMID:9744877 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0009425 increased soleus weight IAGP N RGD:5509061 20141003 MGI PMID:9744877 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20220519 MGI PMID:28797108 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:18252746 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:9744877 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20220519 MGI PMID:28797108 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0010106 abnormal circulating pyruvate kinase level IAGP N RGD:5509061 20141003 MGI PMID:9744877 1317617 Sgca sarcoglycan, alpha (dystrophin-associated glycoprotein) gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:21890494 1317619 Stard5 StAR related lipid transfer domain containing 5 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20160804 MGI 1317619 Stard5 StAR related lipid transfer domain containing 5 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1317619 Stard5 StAR related lipid transfer domain containing 5 gene MP:0004600 abnormal vertebral transverse process morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1317620 Mpv17l2 MPV17 mitochondrial membrane protein-like 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 1317620 Mpv17l2 MPV17 mitochondrial membrane protein-like 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20181227 MGI 1317620 Mpv17l2 MPV17 mitochondrial membrane protein-like 2 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20210128 MGI 1317620 Mpv17l2 MPV17 mitochondrial membrane protein-like 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20181227 MGI 1317620 Mpv17l2 MPV17 mitochondrial membrane protein-like 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 1317620 Mpv17l2 MPV17 mitochondrial membrane protein-like 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20181227 MGI 1317621 2610318N02Rik RIKEN cDNA 2610318N02 gene gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210520 MGI 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:21859843 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:19151727 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:19151727 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16465592 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:21490399 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21490399 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22898778 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21490399 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20190307 MGI PMID:25625206 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:22898778 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21859843 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:22898778 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0003228 abnormal sinus venosus morphology IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0003410 abnormal artery development IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0003542 abnormal vascular endothelial cell development IAGP N RGD:5509061 20141003 MGI PMID:19151727 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21490399 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19151727 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004266 pale placenta IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:19151727 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:19151727 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:21859843 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16465592 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21490399 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21859843 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20190307 MGI PMID:27513872 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:19151727 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16037064 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0006052 cerebellum hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0006052 cerebellum hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21859843 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21859843 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:21490399 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0006338 abnormal second pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0006339 abnormal third pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0010355 abnormal first pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0010356 abnormal second pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0010463 aorta stenosis IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21859843 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16465592 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19151727 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19151728 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22898778 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190307 MGI PMID:25625206 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22898778 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20240118 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0011514 skin hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21859843 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20240118 MGI PMID:19259391 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0012511 dilated aortic sac IAGP N RGD:5509061 20141003 MGI PMID:19151727 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0030044 short forehead IAGP N RGD:5509061 20170921 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:21596842 1317624 Ccm2 cerebral cavernous malformation 2 gene MP:0031593 decreased cardiac jelly amount IAGP N RGD:5509061 20240229 MGI PMID:25625206 1317626 Zfp346 zinc finger protein 346 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20220811 MGI 1317626 Zfp346 zinc finger protein 346 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1317628 Osbp oxysterol binding protein gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20230119 MGI 1317628 Osbp oxysterol binding protein gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1317628 Osbp oxysterol binding protein gene MP:0001714 absent trophoblast giant cells IEA N RGD:5509061 20241017 MGI 1317628 Osbp oxysterol binding protein gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241017 MGI 1317628 Osbp oxysterol binding protein gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1317628 Osbp oxysterol binding protein gene MP:0004964 absent inner cell mass IEA N RGD:5509061 20241017 MGI 1317628 Osbp oxysterol binding protein gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1317628 Osbp oxysterol binding protein gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1317628 Osbp oxysterol binding protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1317628 Osbp oxysterol binding protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230119 MGI 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0000015 abnormal ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:6031677 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:6031677 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:6031677 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:6031677 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0002963 decreased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:417081 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0002963 decreased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:6232310 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0003173 decreased lysosomal enzyme secretion IAGP N RGD:5509061 20141003 MGI PMID:10739679 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0003173 decreased lysosomal enzyme secretion IAGP N RGD:5509061 20141003 MGI PMID:417081 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0003174 increased lysosomal enzyme secretion IAGP N RGD:5509061 20141003 MGI PMID:6696991 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:864040 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0004721 abnormal platelet dense granule morphology IAGP N RGD:5509061 20141003 MGI PMID:6696991 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:2369371 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:6696991 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:12445206 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:6031677 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0005100 abnormal choroid pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11836498 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11836498 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:2369371 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:3516713 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:6696991 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20160114 MGI PMID:25477496 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20160114 MGI PMID:25477496 1317630 Hps4 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2 gene MP:0011279 decreased ear pigmentation IAGP N RGD:5509061 20170803 MGI PMID:864040 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0001401 jumpy IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0008509 disorganized retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0008583 absent photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20399730 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0010236 abnormal retina outer limiting membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:22398208 1317632 Pals1 protein associated with LIN7 1, MAGUK family member gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:22398208 1317634 Dhx15 DEAH-box helicase 15 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230119 MGI 1317634 Dhx15 DEAH-box helicase 15 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20200402 MGI PMID:31921164 1317634 Dhx15 DEAH-box helicase 15 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230119 MGI 1317634 Dhx15 DEAH-box helicase 15 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1317634 Dhx15 DEAH-box helicase 15 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20200402 MGI PMID:31921164 1317634 Dhx15 DEAH-box helicase 15 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1317634 Dhx15 DEAH-box helicase 15 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20230119 MGI 1317634 Dhx15 DEAH-box helicase 15 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241010 MGI 1317634 Dhx15 DEAH-box helicase 15 gene MP:0003900 shortened QT interval IEA N RGD:5509061 20230119 MGI 1317634 Dhx15 DEAH-box helicase 15 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20200402 MGI PMID:31921164 1317634 Dhx15 DEAH-box helicase 15 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200402 MGI PMID:31921164 1317634 Dhx15 DEAH-box helicase 15 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20200402 MGI PMID:31921164 1317634 Dhx15 DEAH-box helicase 15 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1317634 Dhx15 DEAH-box helicase 15 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200402 MGI PMID:31921164 1317634 Dhx15 DEAH-box helicase 15 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200402 MGI PMID:31921164 1317634 Dhx15 DEAH-box helicase 15 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20200402 MGI PMID:31921164 1317634 Dhx15 DEAH-box helicase 15 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230119 MGI 1317634 Dhx15 DEAH-box helicase 15 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1317634 Dhx15 DEAH-box helicase 15 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241010 MGI 1317637 Plxna4 plexin A4 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1317637 Plxna4 plexin A4 gene MP:0000601 small liver IEA N RGD:5509061 20230119 MGI 1317637 Plxna4 plexin A4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1317637 Plxna4 plexin A4 gene MP:0000692 small spleen IEA N RGD:5509061 20230119 MGI 1317637 Plxna4 plexin A4 gene MP:0000861 disorganized barrel cortex IAGP N RGD:5509061 20141003 MGI PMID:15814794 1317637 Plxna4 plexin A4 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:21270798 1317637 Plxna4 plexin A4 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15721238 1317637 Plxna4 plexin A4 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15814794 1317637 Plxna4 plexin A4 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15814794 1317637 Plxna4 plexin A4 gene MP:0001063 abnormal trochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15721238 1317637 Plxna4 plexin A4 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15721238 1317637 Plxna4 plexin A4 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15814794 1317637 Plxna4 plexin A4 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15814794 1317637 Plxna4 plexin A4 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15814794 1317637 Plxna4 plexin A4 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15814794 1317637 Plxna4 plexin A4 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15814794 1317637 Plxna4 plexin A4 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1317637 Plxna4 plexin A4 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 1317637 Plxna4 plexin A4 gene MP:0001258 decreased body length IEA N RGD:5509061 20230119 MGI 1317637 Plxna4 plexin A4 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 1317637 Plxna4 plexin A4 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1317637 Plxna4 plexin A4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1317637 Plxna4 plexin A4 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20231207 MGI 1317637 Plxna4 plexin A4 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1317637 Plxna4 plexin A4 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17296555 1317637 Plxna4 plexin A4 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20484647 1317637 Plxna4 plexin A4 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15721238 1317637 Plxna4 plexin A4 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15814794 1317637 Plxna4 plexin A4 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21270798 1317637 Plxna4 plexin A4 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 1317637 Plxna4 plexin A4 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20230119 MGI 1317637 Plxna4 plexin A4 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21270798 1317637 Plxna4 plexin A4 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:15814794 1317637 Plxna4 plexin A4 gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:15721238 1317637 Plxna4 plexin A4 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20230119 MGI 1317637 Plxna4 plexin A4 gene MP:0008312 abnormal sympathetic postganglionic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15814794 1317637 Plxna4 plexin A4 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:21270798 1317637 Plxna4 plexin A4 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17296555 1317637 Plxna4 plexin A4 gene MP:0010859 abnormal anterior commissure pars anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:15814794 1317637 Plxna4 plexin A4 gene MP:0010860 abnormal anterior commissure pars posterior morphology IAGP N RGD:5509061 20141003 MGI PMID:15814794 1317638 Tekt4 tektin 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17244819 1317638 Tekt4 tektin 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:18951373 1317638 Tekt4 tektin 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17244819 1317638 Tekt4 tektin 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17244819 1317638 Tekt4 tektin 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18951373 1317638 Tekt4 tektin 4 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:17244819 1317638 Tekt4 tektin 4 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17244819 1317638 Tekt4 tektin 4 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:17244819 1317638 Tekt4 tektin 4 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20180621 MGI PMID:17244819 1317641 Nrg3 neuregulin 3 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:10723730 1317641 Nrg3 neuregulin 3 gene MP:0000629 absent mammary gland IAGP N RGD:5509061 20141003 MGI PMID:10723730 1317641 Nrg3 neuregulin 3 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20190328 MGI PMID:27606322 1317641 Nrg3 neuregulin 3 gene MP:0002635 reduced sensorimotor gating IAGP N RGD:5509061 20190328 MGI PMID:27606322 1317641 Nrg3 neuregulin 3 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20190328 MGI PMID:27606322 1317641 Nrg3 neuregulin 3 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20190328 MGI PMID:27606322 1317641 Nrg3 neuregulin 3 gene MP:0009720 abnormal mammary gland pattern IAGP N RGD:5509061 20141003 MGI PMID:10723730 1317641 Nrg3 neuregulin 3 gene MP:0009721 increased mammary gland number IAGP N RGD:5509061 20141003 MGI PMID:10723730 1317641 Nrg3 neuregulin 3 gene MP:0009722 abnormal nipple development IAGP N RGD:5509061 20141003 MGI PMID:10723730 1317641 Nrg3 neuregulin 3 gene MP:0009723 increased nipple number IAGP N RGD:5509061 20141003 MGI PMID:10723730 1317641 Nrg3 neuregulin 3 gene MP:0009724 ectopic nipples IAGP N RGD:5509061 20141003 MGI PMID:10723730 1317641 Nrg3 neuregulin 3 gene MP:0009741 ectopic mammary gland IAGP N RGD:5509061 20141003 MGI PMID:10723730 1317643 Rad21 RAD21 cohesin complex component gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:20971813 1317643 Rad21 RAD21 cohesin complex component gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21832993 1317643 Rad21 RAD21 cohesin complex component gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21832993 1317643 Rad21 RAD21 cohesin complex component gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:21832993 1317643 Rad21 RAD21 cohesin complex component gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:20971813 1317643 Rad21 RAD21 cohesin complex component gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21832993 1317643 Rad21 RAD21 cohesin complex component gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21832993 1317643 Rad21 RAD21 cohesin complex component gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21832993 1317643 Rad21 RAD21 cohesin complex component gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20971813 1317647 Papss1 3'-phosphoadenosine 5'-phosphosulfate synthase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0000297 abnormal atrioventricular cushion morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0000706 small thymus IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0001061 abnormal oculomotor nerve morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0001092 abnormal trigeminal ganglion morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0002177 abnormal outer ear morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0002951 small thyroid gland IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0003078 aphakia IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0004160 retroesophageal right subclavian artery IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0005262 coloboma IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20221215 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20221215 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0006093 arteriovenous malformation IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0008922 abnormal cervical rib IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0008923 thoracoschisis IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0009274 buphthalmos IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0009569 abnormal left lung morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0009570 abnormal right lung morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20221215 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0010259 anterior polar cataract IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0010263 total cataract IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0010439 abnormal hepatic vein morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0010463 aorta stenosis IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0010484 bicuspid aortic valve IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0010713 corneal-lenticular stalk IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20160310 MGI PMID:17179069 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0013162 abnormal thyroid gland isthmus morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0013163 absent thyroid gland isthmus IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0013867 abnormal ventral pancreas morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0013875 increased trigeminal neuroma incidence IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0013913 absent costovertebral joint IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0013936 abnormal thymus topology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0014003 additional anastomosis between intracranial vertebral arteries IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0014012 abnormal cranial blood vasculature morphology IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0014018 embryo tumor IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0014019 embryo cyst IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0014021 heterochrony IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0014023 abnormal intestine placement IEA N RGD:5509061 20180628 MGI 1317653 Col4a2 collagen, type IV, alpha 2 gene MP:0014087 retrolental blood IEA N RGD:5509061 20180628 MGI 1317657 Ap5m1 adaptor-related protein complex 5, mu 1 subunit gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1317657 Ap5m1 adaptor-related protein complex 5, mu 1 subunit gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1317657 Ap5m1 adaptor-related protein complex 5, mu 1 subunit gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1317657 Ap5m1 adaptor-related protein complex 5, mu 1 subunit gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1317657 Ap5m1 adaptor-related protein complex 5, mu 1 subunit gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20231207 MGI 1317657 Ap5m1 adaptor-related protein complex 5, mu 1 subunit gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20231207 MGI 1317657 Ap5m1 adaptor-related protein complex 5, mu 1 subunit gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1317661 Phykpl 5-phosphohydroxy-L-lysine phospholyase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20141003 MGI 1317661 Phykpl 5-phosphohydroxy-L-lysine phospholyase gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1317661 Phykpl 5-phosphohydroxy-L-lysine phospholyase gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20141003 MGI 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20200730 MGI PMID:32169121 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20190103 MGI PMID:28545977 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190103 MGI PMID:28545977 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190103 MGI PMID:28545977 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20200730 MGI PMID:32169121 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20200730 MGI PMID:32169121 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20200730 MGI PMID:32169121 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20200730 MGI PMID:32169121 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20200730 MGI PMID:32169121 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20200730 MGI PMID:32169121 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20190103 MGI PMID:28545977 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200730 MGI PMID:32169121 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20200730 MGI PMID:32169121 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0010028 aciduria IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20200730 MGI PMID:32169121 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0010742 increased Schwann cell number IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20200730 MGI PMID:32169121 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20200730 MGI PMID:32169121 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20200730 MGI PMID:32169121 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0011904 abnormal Schwann cell physiology IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20181227 MGI PMID:29661920 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0012674 tomacula IAGP N RGD:5509061 20200730 MGI PMID:32169121 1317664 Dhtkd1 dehydrogenase E1 and transketolase domain containing 1 gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20190103 MGI PMID:28545977 1317665 Arhgef40 Rho guanine nucleotide exchange factor 40 gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20231207 MGI 1317668 Btf3 basic transcription factor 3 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230119 MGI 1317668 Btf3 basic transcription factor 3 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230119 MGI 1317668 Btf3 basic transcription factor 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1317668 Btf3 basic transcription factor 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1317668 Btf3 basic transcription factor 3 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1317668 Btf3 basic transcription factor 3 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20230119 MGI 1317668 Btf3 basic transcription factor 3 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1317668 Btf3 basic transcription factor 3 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1317668 Btf3 basic transcription factor 3 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20141003 MGI PMID:7655515 1317668 Btf3 basic transcription factor 3 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230119 MGI 1317668 Btf3 basic transcription factor 3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7655515 1317668 Btf3 basic transcription factor 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1317668 Btf3 basic transcription factor 3 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20230119 MGI 1317670 Cuedc2 CUE domain containing 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20191003 MGI PMID:24882011 1317670 Cuedc2 CUE domain containing 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20191003 MGI PMID:24882011 1317670 Cuedc2 CUE domain containing 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20191003 MGI PMID:24882011 1317670 Cuedc2 CUE domain containing 2 gene MP:0011078 increased macrophage cytokine production IAGP N RGD:5509061 20191003 MGI PMID:24882011 1317672 Actn2 actinin alpha 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20230601 MGI PMID:36899856 1317672 Actn2 actinin alpha 2 gene MP:0000486 abnormal pulmonary trunk morphology IAGP N RGD:5509061 20230601 MGI PMID:36899856 1317672 Actn2 actinin alpha 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20230601 MGI PMID:36899856 1317672 Actn2 actinin alpha 2 gene MP:0002748 abnormal pulmonary valve morphology IAGP N RGD:5509061 20230601 MGI PMID:36899856 1317672 Actn2 actinin alpha 2 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20230601 MGI PMID:36899856 1317672 Actn2 actinin alpha 2 gene MP:0003923 abnormal heart left atrium morphology IAGP N RGD:5509061 20230601 MGI PMID:36899856 1317672 Actn2 actinin alpha 2 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20230601 MGI PMID:36899856 1317672 Actn2 actinin alpha 2 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20230601 MGI PMID:36899856 1317672 Actn2 actinin alpha 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20230601 MGI PMID:36899856 1317672 Actn2 actinin alpha 2 gene MP:0010463 aorta stenosis IAGP N RGD:5509061 20230601 MGI PMID:36899856 1317672 Actn2 actinin alpha 2 gene MP:0010605 thick pulmonary valve cusps IAGP N RGD:5509061 20231221 MGI PMID:36899856 1317672 Actn2 actinin alpha 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20230601 MGI PMID:36899856 1317672 Actn2 actinin alpha 2 gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20230601 MGI PMID:36899856 1317672 Actn2 actinin alpha 2 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20230601 MGI PMID:36899856 1317672 Actn2 actinin alpha 2 gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20230601 MGI PMID:36899856 1317677 Tbcd tubulin-specific chaperone d gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1317677 Tbcd tubulin-specific chaperone d gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1317681 Plac8 placenta-specific 8 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17404296 1317681 Plac8 placenta-specific 8 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17404296 1317681 Plac8 placenta-specific 8 gene MP:0001260 increased body weight IAGP N RGD:5509061 20180111 MGI PMID:21982742 1317681 Plac8 placenta-specific 8 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1317681 Plac8 placenta-specific 8 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1317681 Plac8 placenta-specific 8 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1317681 Plac8 placenta-specific 8 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1317681 Plac8 placenta-specific 8 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20181227 MGI 1317681 Plac8 placenta-specific 8 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17404296 1317681 Plac8 placenta-specific 8 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17404296 1317681 Plac8 placenta-specific 8 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1317681 Plac8 placenta-specific 8 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1317681 Plac8 placenta-specific 8 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:17404296 1317681 Plac8 placenta-specific 8 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20180111 MGI PMID:21982742 1317681 Plac8 placenta-specific 8 gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20180111 MGI PMID:21982742 1317681 Plac8 placenta-specific 8 gene MP:0009137 decreased brown fat lipid droplet number IAGP N RGD:5509061 20180111 MGI PMID:21982742 1317681 Plac8 placenta-specific 8 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:21982742 1317681 Plac8 placenta-specific 8 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20180111 MGI PMID:21982742 1317681 Plac8 placenta-specific 8 gene MP:0020520 whitened brown adipose tissue morphology IAGP N RGD:5509061 20180208 MGI PMID:21982742 1317683 Usp39 ubiquitin specific peptidase 39 gene MP:0001192 scaly skin IAGP N RGD:5509061 20220630 MGI PMID:35440748 1317683 Usp39 ubiquitin specific peptidase 39 gene MP:0001200 thick skin IAGP N RGD:5509061 20220630 MGI PMID:35440748 1317683 Usp39 ubiquitin specific peptidase 39 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20220630 MGI PMID:35440748 1317683 Usp39 ubiquitin specific peptidase 39 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20220630 MGI PMID:35440748 1317683 Usp39 ubiquitin specific peptidase 39 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20220630 MGI PMID:35440748 1317683 Usp39 ubiquitin specific peptidase 39 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20170105 MGI 1317683 Usp39 ubiquitin specific peptidase 39 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20220630 MGI PMID:35440748 1317683 Usp39 ubiquitin specific peptidase 39 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20220630 MGI PMID:35440748 1317683 Usp39 ubiquitin specific peptidase 39 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20220630 MGI PMID:35440748 1317683 Usp39 ubiquitin specific peptidase 39 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1317683 Usp39 ubiquitin specific peptidase 39 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20220630 MGI PMID:35440748 1317683 Usp39 ubiquitin specific peptidase 39 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20220630 MGI PMID:35440748 1317683 Usp39 ubiquitin specific peptidase 39 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20220630 MGI PMID:35440748 1317683 Usp39 ubiquitin specific peptidase 39 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20220630 MGI PMID:35440748 1317683 Usp39 ubiquitin specific peptidase 39 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20220630 MGI PMID:35440748 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12874031 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12874031 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:12874031 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:12874031 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12874031 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:12874031 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:12874031 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:12874031 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16731514 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:16731514 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:16731514 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:17056543 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:12874031 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:12874031 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:12874031 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16107706 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11940661 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12874031 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:16107706 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11940661 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:16731514 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:11940661 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:16107706 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16731514 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16731514 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:11940661 1317687 Ksr1 kinase suppressor of ras 1 gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:12874031 1317692 Cabp5 calcium binding protein 5 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20210128 MGI 1317692 Cabp5 calcium binding protein 5 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20191114 MGI PMID:18586882 1317692 Cabp5 calcium binding protein 5 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1317701 Sugct succinyl-CoA glutarate-CoA transferase gene MP:0001260 increased body weight IAGP N RGD:5509061 20201015 MGI PMID:31722069 1317701 Sugct succinyl-CoA glutarate-CoA transferase gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20201015 MGI PMID:31722069 1317701 Sugct succinyl-CoA glutarate-CoA transferase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20201015 MGI PMID:31722069 1317701 Sugct succinyl-CoA glutarate-CoA transferase gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20201015 MGI PMID:31722069 1317701 Sugct succinyl-CoA glutarate-CoA transferase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20201015 MGI PMID:31722069 1317701 Sugct succinyl-CoA glutarate-CoA transferase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20201015 MGI PMID:31722069 1317701 Sugct succinyl-CoA glutarate-CoA transferase gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20201015 MGI PMID:31722069 1317701 Sugct succinyl-CoA glutarate-CoA transferase gene MP:0003675 kidney cyst IAGP N RGD:5509061 20201015 MGI PMID:31722069 1317701 Sugct succinyl-CoA glutarate-CoA transferase gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20201015 MGI PMID:31722069 1317701 Sugct succinyl-CoA glutarate-CoA transferase gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20201015 MGI PMID:31722069 1317701 Sugct succinyl-CoA glutarate-CoA transferase gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20201015 MGI PMID:31722069 1317701 Sugct succinyl-CoA glutarate-CoA transferase gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20201015 MGI PMID:31722069 1317701 Sugct succinyl-CoA glutarate-CoA transferase gene MP:0010999 proteinosis IAGP N RGD:5509061 20201015 MGI PMID:31722069 1317701 Sugct succinyl-CoA glutarate-CoA transferase gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20201015 MGI PMID:31722069 1317701 Sugct succinyl-CoA glutarate-CoA transferase gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240418 MGI PMID:31722069 1317703 Aatk apoptosis-associated tyrosine kinase gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:22573681 1317703 Aatk apoptosis-associated tyrosine kinase gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:22573681 1317703 Aatk apoptosis-associated tyrosine kinase gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22573681 1317703 Aatk apoptosis-associated tyrosine kinase gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:22573681 1317705 9930012K11Rik RIKEN cDNA 9930012K11 gene gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20230601 MGI 1317705 9930012K11Rik RIKEN cDNA 9930012K11 gene gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20201231 MGI 1317705 9930012K11Rik RIKEN cDNA 9930012K11 gene gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20211021 MGI 1317707 Sh3bgrl3 SH3 domain binding glutamic acid-rich protein-like 3 gene MP:0013406 abnormal epidermal immune compartment IEA N RGD:5509061 20201231 MGI 1317711 Zfp207 zinc finger protein 207 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1317711 Zfp207 zinc finger protein 207 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1317711 Zfp207 zinc finger protein 207 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1317711 Zfp207 zinc finger protein 207 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1317711 Zfp207 zinc finger protein 207 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20240523 MGI 1317711 Zfp207 zinc finger protein 207 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317713 Gna14 guanine nucleotide binding protein, alpha 14 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 1317717 Slc35f5 solute carrier family 35, member F5 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20230119 MGI 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210128 MGI 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210128 MGI 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20201022 MGI 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0002764 short tibia IEA N RGD:5509061 20230601 MGI 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20230105 MGI PMID:36217001 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20230105 MGI PMID:36217001 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20230105 MGI PMID:36217001 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20230105 MGI PMID:36217001 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200514 MGI 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210128 MGI 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20230105 MGI PMID:36217001 1317727 Arih1 ariadne RBR E3 ubiquitin protein ligase 1 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20230105 MGI PMID:36217001 1317730 Fam135b family with sequence similarity 135, member B gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220519 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20180621 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20150430 MGI PMID:24778225 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20150430 MGI PMID:24778225 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180621 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001406 abnormal gait IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001781 abnormal white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20161222 MGI PMID:24358199 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20180621 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001925 male infertility IAGP N RGD:5509061 20150430 MGI PMID:24778225 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20150430 MGI PMID:24778225 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20150430 MGI PMID:24778225 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20200402 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20150430 MGI PMID:24778225 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20150430 MGI PMID:24778225 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20161222 MGI PMID:24358199 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20180621 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20180621 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20180621 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20150430 MGI PMID:24778225 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20150430 MGI PMID:24778225 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20200402 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20150430 MGI PMID:24778225 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180621 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20161222 MGI PMID:24358199 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20161222 MGI PMID:24358199 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20150430 MGI PMID:24778225 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20150430 MGI PMID:24778225 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20180621 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20150430 MGI PMID:24778225 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20150430 MGI PMID:24778225 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009303 decreased renal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180621 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20180621 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20180621 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0011156 abnormal hypodermis fat layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0011169 abnormal white fat cell differentation IAGP N RGD:5509061 20141003 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20150430 MGI PMID:24778225 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20180621 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0011941 increased fluid intake IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20161222 MGI PMID:24358199 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20180621 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20180621 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0020521 browned white adipose tissue morphology IAGP N RGD:5509061 20180621 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0030880 abnormal infrapatellar fat pad morphology IAGP N RGD:5509061 20181101 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:22269949 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:23680914 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0031008 decreased bone marrow adipose tissue amount IAGP N RGD:5509061 20200130 MGI PMID:29459250 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21551454 1317733 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21551454 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20160811 MGI 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0001147 small testis IEA N RGD:5509061 20160811 MGI 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:20081859 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0001326 retina degeneration IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18684731 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18684731 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20141003 MGI PMID:18684731 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18684731 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:18684731 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0004906 enlarged uterus IEA N RGD:5509061 20170105 MGI 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18684731 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20081859 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:18684731 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0009709 hydrometra IEA N RGD:5509061 20170105 MGI 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0011308 kidney corticomedullary cyst IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0011408 renal tubule hypertrophy IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0013305 isosthenuria IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317735 Nphp1 nephronophthisis 1 (juvenile) homolog (human) gene MP:0031358 decreased urine output IAGP N RGD:5509061 20220609 MGI PMID:34415307 1317737 Gmnn geminin gene MP:0000216 absent erythroid progenitor cell IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17054725 1317737 Gmnn geminin gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20107189 1317737 Gmnn geminin gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20141003 MGI 1317737 Gmnn geminin gene MP:0001304 cataract IEA N RGD:5509061 20141003 MGI 1317737 Gmnn geminin gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16847348 1317737 Gmnn geminin gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21408022 1317737 Gmnn geminin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:17054725 1317737 Gmnn geminin gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16847348 1317737 Gmnn geminin gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:17054725 1317737 Gmnn geminin gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:17054725 1317737 Gmnn geminin gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:16847348 1317737 Gmnn geminin gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:16847348 1317737 Gmnn geminin gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16847348 1317737 Gmnn geminin gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16847348 1317737 Gmnn geminin gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20107189 1317737 Gmnn geminin gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20107189 1317737 Gmnn geminin gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:20107189 1317737 Gmnn geminin gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20107189 1317737 Gmnn geminin gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20107189 1317737 Gmnn geminin gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:16847348 1317737 Gmnn geminin gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:17054725 1317737 Gmnn geminin gene MP:0010130 decreased DN1 thymic pro-T cell number IAGP N RGD:5509061 20141003 MGI PMID:20107189 1317737 Gmnn geminin gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20107189 1317737 Gmnn geminin gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:20107189 1317737 Gmnn geminin gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16847348 1317737 Gmnn geminin gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17054725 1317737 Gmnn geminin gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20107189 1317737 Gmnn geminin gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0011903 decreased hematopoietic stem cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21041951 1317737 Gmnn geminin gene MP:0012102 absent trophectoderm IAGP N RGD:5509061 20141003 MGI PMID:17054725 1317738 Zpld1 zona pellucida like domain containing 1 gene MP:0001394 circling IAGP N RGD:5509061 20191128 MGI PMID:31455802 1317738 Zpld1 zona pellucida like domain containing 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20191128 MGI PMID:31455802 1317738 Zpld1 zona pellucida like domain containing 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20191128 MGI PMID:31455802 1317738 Zpld1 zona pellucida like domain containing 1 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20191128 MGI PMID:31455802 1317738 Zpld1 zona pellucida like domain containing 1 gene MP:0004844 abnormal vestibuloocular reflex IAGP N RGD:5509061 20191128 MGI PMID:31455802 1317738 Zpld1 zona pellucida like domain containing 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1317738 Zpld1 zona pellucida like domain containing 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1317739 Ncbp3 nuclear cap binding subunit 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1317739 Ncbp3 nuclear cap binding subunit 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1317739 Ncbp3 nuclear cap binding subunit 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1317739 Ncbp3 nuclear cap binding subunit 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1317744 Chst1 carbohydrate sulfotransferase 1 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:23254996 1317744 Chst1 carbohydrate sulfotransferase 1 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:23254996 1317744 Chst1 carbohydrate sulfotransferase 1 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23254996 1317744 Chst1 carbohydrate sulfotransferase 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23254996 1317745 Ppip5k2 diphosphoinositol pentakisphosphate kinase 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20181004 MGI PMID:29590114 1317745 Ppip5k2 diphosphoinositol pentakisphosphate kinase 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20181004 MGI PMID:29590114 1317745 Ppip5k2 diphosphoinositol pentakisphosphate kinase 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1317745 Ppip5k2 diphosphoinositol pentakisphosphate kinase 2 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20181004 MGI PMID:29590114 1317745 Ppip5k2 diphosphoinositol pentakisphosphate kinase 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20191219 MGI PMID:29590114 1317747 Ergic3 ERGIC and golgi 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20240229 MGI PMID:34994051 1317747 Ergic3 ERGIC and golgi 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20240229 MGI PMID:34994051 1317747 Ergic3 ERGIC and golgi 3 gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20240229 MGI PMID:34994051 1317747 Ergic3 ERGIC and golgi 3 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20240229 MGI PMID:34994051 1317747 Ergic3 ERGIC and golgi 3 gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20240229 MGI PMID:34994051 1317747 Ergic3 ERGIC and golgi 3 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20240229 MGI PMID:34994051 1317747 Ergic3 ERGIC and golgi 3 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20240229 MGI PMID:34994051 1317749 Phf13 PHD finger protein 13 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:21852425 1317749 Phf13 PHD finger protein 13 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21852425 1317749 Phf13 PHD finger protein 13 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21852425 1317749 Phf13 PHD finger protein 13 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:21852425 1317749 Phf13 PHD finger protein 13 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21852425 1317749 Phf13 PHD finger protein 13 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21852425 1317749 Phf13 PHD finger protein 13 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:21852425 1317749 Phf13 PHD finger protein 13 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:21852425 1317749 Phf13 PHD finger protein 13 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21852425 1317749 Phf13 PHD finger protein 13 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21852425 1317749 Phf13 PHD finger protein 13 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:21852425 1317749 Phf13 PHD finger protein 13 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21852425 1317749 Phf13 PHD finger protein 13 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21852425 1317749 Phf13 PHD finger protein 13 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21852425 1317749 Phf13 PHD finger protein 13 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21852425 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0031550 abnormal atrioventricular valve development IAGP N RGD:5509061 20240104 MGI PMID:20549726 1317751 Shoc2 Shoc2, leucine rich repeat scaffold protein gene MP:0031553 abnormal semilunar valve development IAGP N RGD:5509061 20240125 MGI PMID:20549726 1317754 Sgo1 shugoshin 1 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22262168 1317754 Sgo1 shugoshin 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160804 MGI 1317754 Sgo1 shugoshin 1 gene MP:0001304 cataract IEA N RGD:5509061 20160804 MGI 1317754 Sgo1 shugoshin 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22262168 1317754 Sgo1 shugoshin 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:22262168 1317754 Sgo1 shugoshin 1 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:22262168 1317754 Sgo1 shugoshin 1 gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20160804 MGI 1317754 Sgo1 shugoshin 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1317754 Sgo1 shugoshin 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1317754 Sgo1 shugoshin 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:22262168 1317754 Sgo1 shugoshin 1 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:22262168 1317754 Sgo1 shugoshin 1 gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20160804 MGI 1317754 Sgo1 shugoshin 1 gene MP:0012436 increased colon tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22262168 1317761 Creb3l3 cAMP responsive element binding protein 3-like 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18704925 1317761 Creb3l3 cAMP responsive element binding protein 3-like 3 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:18704925 1317761 Creb3l3 cAMP responsive element binding protein 3-like 3 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23409047 1317761 Creb3l3 cAMP responsive element binding protein 3-like 3 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23409047 1317761 Creb3l3 cAMP responsive element binding protein 3-like 3 gene MP:0031233 decreased circulating serum amyloid protein level IAGP N RGD:5509061 20210225 MGI PMID:18704925 1317763 Xxylt1 xyloside xylosyltransferase 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1317763 Xxylt1 xyloside xylosyltransferase 1 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20181227 MGI 1317763 Xxylt1 xyloside xylosyltransferase 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1317763 Xxylt1 xyloside xylosyltransferase 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1317767 Misp mitotic spindle positioning gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20230622 MGI PMID:36596561 1317767 Misp mitotic spindle positioning gene MP:0003292 melena IAGP N RGD:5509061 20230622 MGI PMID:36596561 1317767 Misp mitotic spindle positioning gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20230622 MGI PMID:36596561 1317767 Misp mitotic spindle positioning gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20230622 MGI PMID:36596561 1317767 Misp mitotic spindle positioning gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20230622 MGI PMID:36596561 1317767 Misp mitotic spindle positioning gene MP:0008838 decreased transforming growth factor beta level IAGP N RGD:5509061 20230622 MGI PMID:36596561 1317767 Misp mitotic spindle positioning gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20230622 MGI PMID:36596561 1317767 Misp mitotic spindle positioning gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20230622 MGI PMID:36596561 1317767 Misp mitotic spindle positioning gene MP:0014222 decreased colon goblet cell number IAGP N RGD:5509061 20230622 MGI PMID:36596561 1317767 Misp mitotic spindle positioning gene MP:0031319 impaired intestine regeneration IAGP N RGD:5509061 20230622 MGI PMID:36596561 1317769 Cul1 cullin 1 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:10508527 1317769 Cul1 cullin 1 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:10531039 1317769 Cul1 cullin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10508527 1317769 Cul1 cullin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10531039 1317769 Cul1 cullin 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10531039 1317769 Cul1 cullin 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20150129 MGI PMID:10508527 1317769 Cul1 cullin 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20150129 MGI PMID:10531039 1317769 Cul1 cullin 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10531039 1317769 Cul1 cullin 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10508527 1317769 Cul1 cullin 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10531039 1317772 Lnx1 ligand of numb-protein X 1 gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20141003 MGI 1317774 Ccdc178 coiled coil domain containing 178 gene MP:0001314 cornea opacity IEA N RGD:5509061 20210128 MGI 1317774 Ccdc178 coiled coil domain containing 178 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1317778 Cnnm2 cyclin M2 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 1317778 Cnnm2 cyclin M2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1317778 Cnnm2 cyclin M2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1317778 Cnnm2 cyclin M2 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20181227 MGI 1317778 Cnnm2 cyclin M2 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1317778 Cnnm2 cyclin M2 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1317778 Cnnm2 cyclin M2 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1317778 Cnnm2 cyclin M2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1317778 Cnnm2 cyclin M2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1317778 Cnnm2 cyclin M2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240627 MGI 1317778 Cnnm2 cyclin M2 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20210429 MGI PMID:28033128 1317778 Cnnm2 cyclin M2 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1317778 Cnnm2 cyclin M2 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1317778 Cnnm2 cyclin M2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1317778 Cnnm2 cyclin M2 gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20210429 MGI PMID:28033128 1317778 Cnnm2 cyclin M2 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20210429 MGI PMID:28033128 1317778 Cnnm2 cyclin M2 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20210429 MGI PMID:28033128 1317778 Cnnm2 cyclin M2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20210429 MGI PMID:28033128 1317778 Cnnm2 cyclin M2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317778 Cnnm2 cyclin M2 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20181227 MGI 1317778 Cnnm2 cyclin M2 gene MP:0011496 abnormal head size IEA N RGD:5509061 20181227 MGI 1317780 Golga5 golgin A5 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180503 MGI PMID:28509431 1317780 Golga5 golgin A5 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1317780 Golga5 golgin A5 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180503 MGI PMID:28509431 1317780 Golga5 golgin A5 gene MP:0000445 short snout IAGP N RGD:5509061 20180503 MGI PMID:28509431 1317780 Golga5 golgin A5 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1317780 Golga5 golgin A5 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20180503 MGI PMID:28509431 1317780 Golga5 golgin A5 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 1317780 Golga5 golgin A5 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1317780 Golga5 golgin A5 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1317780 Golga5 golgin A5 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220519 MGI 1317783 Msantd3 Myb/SANT-like DNA-binding domain containing 3 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20231207 MGI 1317783 Msantd3 Myb/SANT-like DNA-binding domain containing 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20201022 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:21673050 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000339 decreased enterocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9697701 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19718027 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20141003 MGI PMID:19718027 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:22393260 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21383188 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9697701 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9697701 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:21383188 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:21383188 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21383188 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000520 absent kidney IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000636 enlarged pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:12907761 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:21828091 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:19718027 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:19718027 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:19718027 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21673050 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21383188 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:19718027 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21673050 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:21673050 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:22393260 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23028378 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22717537 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21828091 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0002239 abnormal nasal septum morphology IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21383188 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21673050 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:22717537 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21383188 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:23028378 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:21828091 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:12907761 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150430 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:21673050 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0004160 retroesophageal right subclavian artery IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0004164 abnormal neurohypophysis morphology IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0004463 basisphenoid bone foramen IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0004609 vertebral fusion IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21673050 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22717537 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23028378 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:19718027 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23028378 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21673050 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0008130 abnormal pituitary intermediate lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:12907761 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0008366 enlarged adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:12907761 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20190103 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21383188 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22393260 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22393260 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:22717537 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:21383188 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:21673050 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19718027 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:21383188 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:21673050 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21673050 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23028378 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20150430 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20141003 MGI PMID:22393260 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0010589 common truncal valve IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0010602 abnormal pulmonary valve cusp morphology IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0010802 abnormal intestinal enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21383188 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21383188 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21673050 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9697701 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23028378 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0011513 abnormal vertebral artery morphology IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0013186 abnormal basilar artery morphology IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:21383188 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20160310 MGI PMID:22393260 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0013792 abnormal small intestine goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:21383188 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0013792 abnormal small intestine goblet cell morphology IAGP N RGD:5509061 20160310 MGI PMID:22393260 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:21383188 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0013862 abnormal cecum position IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0013879 duplication of ductus venosus IEA N RGD:5509061 20180628 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0013943 abnormal ureter topology IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0013945 abnormal elbow joint morphology IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0013977 symmetric azygos veins IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0013985 abnormal umbilical vein topology IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0014076 absent Paneth cells IAGP N RGD:5509061 20160310 MGI PMID:22393260 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0014077 ectopic Paneth cells IAGP N RGD:5509061 20160310 MGI PMID:22393260 1317787 Tcf7l2 transcription factor 7 like 2, T cell specific, HMG box gene MP:0020485 abnormal inferior vena cava topology IEA N RGD:5509061 20180628 MGI 1317788 Rnf213 ring finger protein 213 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23410753 1317788 Rnf213 ring finger protein 213 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160407 MGI PMID:26315378 1317788 Rnf213 ring finger protein 213 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:23410753 1317788 Rnf213 ring finger protein 213 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:23410753 1317788 Rnf213 ring finger protein 213 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20160304 MGI PMID:25446450 1317788 Rnf213 ring finger protein 213 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20160304 MGI PMID:25446450 1317788 Rnf213 ring finger protein 213 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:23410753 1317788 Rnf213 ring finger protein 213 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23410753 1317788 Rnf213 ring finger protein 213 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23410753 1317788 Rnf213 ring finger protein 213 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23410753 1317788 Rnf213 ring finger protein 213 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23410753 1317788 Rnf213 ring finger protein 213 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:23410753 1317794 Ogn osteoglycin gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1317794 Ogn osteoglycin gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:12432342 1317794 Ogn osteoglycin gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1317794 Ogn osteoglycin gene MP:0003966 abnormal adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:21664248 1317794 Ogn osteoglycin gene MP:0005275 abnormal skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:12432342 1317794 Ogn osteoglycin gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:12432342 1317794 Ogn osteoglycin gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1317794 Ogn osteoglycin gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23056351 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23056351 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20141003 MGI PMID:23056351 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:23056351 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:23056351 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:23056351 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0008031 decreased Cajal-Retzius cell number IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0008440 abnormal subplate morphology IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23056351 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317797 Dmrta2 doublesex and mab-3 related transcription factor like family A2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20150205 MGI PMID:22923088 1317799 Fign fidgetin gene MP:0000035 abnormal membranous labyrinth morphology IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:11017077 1317799 Fign fidgetin gene MP:0000039 abnormal otic capsule morphology IEA N RGD:5509061 20181025 MGI 1317799 Fign fidgetin gene MP:0000458 abnormal mandible morphology IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0000562 polydactyly IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0000929 open neural tube IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0001262 decreased body weight IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11017077 1317799 Fign fidgetin gene MP:0001306 small lens IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0001314 cornea opacity IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0001347 absent lacrimal glands IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0001386 abnormal maternal nurturing IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0001395 bidirectional circling IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0001405 impaired coordination IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0001488 increased startle reflex IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:16751186 1317799 Fign fidgetin gene MP:0001732 postnatal growth retardation IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0001851 eye inflammation IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0001852 conjunctivitis IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0001921 reduced fertility IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16751186 1317799 Fign fidgetin gene MP:0001967 deafness IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0002116 abnormal craniofacial bone morphology IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:11017077 1317799 Fign fidgetin gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:11017077 1317799 Fign fidgetin gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:1001817 1317799 Fign fidgetin gene MP:0003161 absent lateral semicircular canal IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0003312 abnormal locomotor coordination IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20150611 MGI PMID:1181211 1317799 Fign fidgetin gene MP:0004452 abnormal pterygoid process morphology IEA N RGD:5509061 20181025 MGI 1317799 Fign fidgetin gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0004748 increased susceptibility to age-related hearing loss IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0005542 cornea vascularization IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20141225 MGI PMID:1001817 1317799 Fign fidgetin gene MP:0006097 abnormal cerebellar lobule formation IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0008919 fused tarsal bones IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141225 MGI PMID:1001817 1317799 Fign fidgetin gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16751186 1317799 Fign fidgetin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16751186 1317799 Fign fidgetin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11017077 1317799 Fign fidgetin gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16751186 1317799 Fign fidgetin gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1317799 Fign fidgetin gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11017077 1317799 Fign fidgetin gene MP:0013387 Meibomian gland hypertrophy IEA N RGD:5509061 20141225 MGI 1317799 Fign fidgetin gene MP:0013447 Harderian gland hypertrophy IEA N RGD:5509061 20150205 MGI 1317799 Fign fidgetin gene MP:0030233 absent mandibular canal IEA N RGD:5509061 20171019 MGI 1317799 Fign fidgetin gene MP:0030235 absent mandibular foramen IEA N RGD:5509061 20171019 MGI 1317799 Fign fidgetin gene MP:0030237 absent mental foramen IEA N RGD:5509061 20171019 MGI 1317799 Fign fidgetin gene MP:0030796 hip dislocation IEA N RGD:5509061 20181018 MGI 1317799 Fign fidgetin gene MP:0030838 abnormal acetabular fossa morphology IEA N RGD:5509061 20181025 MGI 1317799 Fign fidgetin gene MP:0030842 absent subarcuate fossa IEA N RGD:5509061 20181025 MGI 1317799 Fign fidgetin gene MP:0031432 cornea perforation IEA N RGD:5509061 20220721 MGI 1317802 Ccnb2 cyclin B2 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:9539739 1317802 Ccnb2 cyclin B2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9539739 1317802 Ccnb2 cyclin B2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9539739 1317802 Ccnb2 cyclin B2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:9539739 1317802 Ccnb2 cyclin B2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9539739 1317806 Sgsm1 small G protein signaling modulator 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1317806 Sgsm1 small G protein signaling modulator 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1317806 Sgsm1 small G protein signaling modulator 1 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20211021 MGI 1317806 Sgsm1 small G protein signaling modulator 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1317810 Ctsf cathepsin F gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16508006 1317810 Ctsf cathepsin F gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16508006 1317810 Ctsf cathepsin F gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16508006 1317810 Ctsf cathepsin F gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:16508006 1317810 Ctsf cathepsin F gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:16508006 1317810 Ctsf cathepsin F gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16508006 1317810 Ctsf cathepsin F gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16508006 1317810 Ctsf cathepsin F gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:16508006 1317810 Ctsf cathepsin F gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16508006 1317810 Ctsf cathepsin F gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:16508006 1317810 Ctsf cathepsin F gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:16508006 1317810 Ctsf cathepsin F gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:16508006 1317810 Ctsf cathepsin F gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:16508006 1317812 Elmo1 engulfment and cell motility 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20141003 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20231109 MGI PMID:36400788 1317812 Elmo1 engulfment and cell motility 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:20844538 1317812 Elmo1 engulfment and cell motility 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20231109 MGI PMID:36400788 1317812 Elmo1 engulfment and cell motility 1 gene MP:0001806 decreased IgM level IEA N RGD:5509061 20181011 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:20844538 1317812 Elmo1 engulfment and cell motility 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20844538 1317812 Elmo1 engulfment and cell motility 1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20844538 1317812 Elmo1 engulfment and cell motility 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0004939 abnormal B cell morphology IEA N RGD:5509061 20190404 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20181011 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20181011 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20150108 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0008037 abnormal T cell morphology IEA N RGD:5509061 20190404 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20190328 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190404 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190328 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20844538 1317812 Elmo1 engulfment and cell motility 1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20231109 MGI PMID:36400788 1317812 Elmo1 engulfment and cell motility 1 gene MP:0009853 decreased Sertoli cell phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:20844538 1317812 Elmo1 engulfment and cell motility 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20150108 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20160804 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20181011 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0010848 decreased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20190328 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36400788 1317812 Elmo1 engulfment and cell motility 1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36400788 1317812 Elmo1 engulfment and cell motility 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36400788 1317812 Elmo1 engulfment and cell motility 1 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36400788 1317812 Elmo1 engulfment and cell motility 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20844538 1317812 Elmo1 engulfment and cell motility 1 gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20231109 MGI PMID:36400788 1317812 Elmo1 engulfment and cell motility 1 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20231109 MGI PMID:36400788 1317812 Elmo1 engulfment and cell motility 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20150108 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:20844538 1317812 Elmo1 engulfment and cell motility 1 gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20181011 MGI 1317812 Elmo1 engulfment and cell motility 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:20844538 1317818 C2cd4b C2 calcium-dependent domain containing 4B gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20201022 MGI 1317818 C2cd4b C2 calcium-dependent domain containing 4B gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1317818 C2cd4b C2 calcium-dependent domain containing 4B gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20181227 MGI 1317818 C2cd4b C2 calcium-dependent domain containing 4B gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1317818 C2cd4b C2 calcium-dependent domain containing 4B gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1317818 C2cd4b C2 calcium-dependent domain containing 4B gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20210128 MGI 1317818 C2cd4b C2 calcium-dependent domain containing 4B gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1317823 Gje1 gap junction protein, epsilon 1 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:18385072 1317823 Gje1 gap junction protein, epsilon 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:18385072 1317823 Gje1 gap junction protein, epsilon 1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:18385072 1317823 Gje1 gap junction protein, epsilon 1 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:18385072 1317823 Gje1 gap junction protein, epsilon 1 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:18385072 1317823 Gje1 gap junction protein, epsilon 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:18385072 1317823 Gje1 gap junction protein, epsilon 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160707 MGI PMID:27038752 1317823 Gje1 gap junction protein, epsilon 1 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18385072 1317823 Gje1 gap junction protein, epsilon 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20240523 MGI 1317823 Gje1 gap junction protein, epsilon 1 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:18385072 1317823 Gje1 gap junction protein, epsilon 1 gene MP:0010258 polar cataract IAGP N RGD:5509061 20141003 MGI PMID:18385072 1317823 Gje1 gap junction protein, epsilon 1 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20230810 MGI PMID:18385072 1317823 Gje1 gap junction protein, epsilon 1 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:18385072 1317825 Cul3 cullin 3 gene MP:0000231 hypertension IAGP N RGD:5509061 20160407 MGI PMID:26286618 1317825 Cul3 cullin 3 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20160407 MGI PMID:26286618 1317825 Cul3 cullin 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17339333 1317825 Cul3 cullin 3 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20200827 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200827 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0000839 hypothalamus hyperplasia IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20160407 MGI PMID:26286618 1317825 Cul3 cullin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160407 MGI PMID:26286618 1317825 Cul3 cullin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200827 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200827 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20160407 MGI PMID:26286618 1317825 Cul3 cullin 3 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:10500095 1317825 Cul3 cullin 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10500095 1317825 Cul3 cullin 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20200827 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20200827 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20200827 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:10500095 1317825 Cul3 cullin 3 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20160407 MGI PMID:26286618 1317825 Cul3 cullin 3 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20200827 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20200827 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17339333 1317825 Cul3 cullin 3 gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20160407 MGI PMID:26286618 1317825 Cul3 cullin 3 gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20170615 MGI PMID:26490675 1317825 Cul3 cullin 3 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20160407 MGI PMID:26286618 1317825 Cul3 cullin 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:17339333 1317825 Cul3 cullin 3 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0004043 abnormal pH regulation IAGP N RGD:5509061 20160407 MGI PMID:26286618 1317825 Cul3 cullin 3 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10500095 1317825 Cul3 cullin 3 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:10500095 1317825 Cul3 cullin 3 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10500095 1317825 Cul3 cullin 3 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200827 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20200827 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0006300 abnormal entorhinal cortex morphology IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0010092 increased circulating magnesium level IAGP N RGD:5509061 20160407 MGI PMID:26286618 1317825 Cul3 cullin 3 gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10500095 1317825 Cul3 cullin 3 gene MP:0010770 preweaning lethality IAGP N RGD:5509061 20200827 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20160407 MGI PMID:26286618 1317825 Cul3 cullin 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17339333 1317825 Cul3 cullin 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20160407 MGI PMID:26286618 1317825 Cul3 cullin 3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10500095 1317825 Cul3 cullin 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20170615 MGI PMID:26490675 1317825 Cul3 cullin 3 gene MP:0012339 hyperkalemia IAGP N RGD:5509061 20160407 MGI PMID:26286618 1317825 Cul3 cullin 3 gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20160407 MGI PMID:26286618 1317825 Cul3 cullin 3 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17339333 1317825 Cul3 cullin 3 gene MP:0014375 increased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20200827 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0020507 increased dendritic spine density IAGP N RGD:5509061 20200827 MGI PMID:31780330 1317825 Cul3 cullin 3 gene MP:0020511 decreased dendritic spine length IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317825 Cul3 cullin 3 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20230706 MGI PMID:33727673 1317827 Guca1b guanylate cyclase activator 1B gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11493703 1317827 Guca1b guanylate cyclase activator 1B gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18723510 1317827 Guca1b guanylate cyclase activator 1B gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21123569 1317827 Guca1b guanylate cyclase activator 1B gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11493703 1317827 Guca1b guanylate cyclase activator 1B gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15173221 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:22575219 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22575219 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:22575219 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20141003 MGI 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22575219 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0001925 male infertility IAGP N RGD:5509061 20220324 MGI PMID:28476888 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20160804 MGI 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:22575219 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220324 MGI PMID:28476888 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220324 MGI PMID:28476888 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0003017 decreased circulating bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:22575219 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0005103 abnormal retina pigmentation IEA N RGD:5509061 20141003 MGI 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20190103 MGI 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20220324 MGI PMID:28476888 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220324 MGI PMID:28476888 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220324 MGI PMID:28476888 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220324 MGI PMID:28476888 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20220324 MGI PMID:28476888 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0013481 abnormal ileum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20150319 MGI PMID:22575219 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:22575219 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220324 MGI PMID:28476888 1317830 Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8 gene MP:0031355 abnormal proacrosomal vesicle fusion IAGP N RGD:5509061 20220324 MGI PMID:28476888 1317832 Nanos1 nanos C2HC-type zinc finger 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12834871 1317833 Slurp2 secreted Ly6/Plaur domain containing 2 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20180621 MGI PMID:26967477 1317833 Slurp2 secreted Ly6/Plaur domain containing 2 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20180621 MGI PMID:26967477 1317833 Slurp2 secreted Ly6/Plaur domain containing 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20180621 MGI PMID:26967477 1317833 Slurp2 secreted Ly6/Plaur domain containing 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180621 MGI PMID:26967477 1317833 Slurp2 secreted Ly6/Plaur domain containing 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20180621 MGI PMID:26967477 1317833 Slurp2 secreted Ly6/Plaur domain containing 2 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20180621 MGI PMID:26967477 1317833 Slurp2 secreted Ly6/Plaur domain containing 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180621 MGI PMID:26967477 1317833 Slurp2 secreted Ly6/Plaur domain containing 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20180621 MGI PMID:26967477 1317833 Slurp2 secreted Ly6/Plaur domain containing 2 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20180621 MGI PMID:26967477 1317833 Slurp2 secreted Ly6/Plaur domain containing 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180621 MGI PMID:26967477 1317833 Slurp2 secreted Ly6/Plaur domain containing 2 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20180621 MGI PMID:26967477 1317833 Slurp2 secreted Ly6/Plaur domain containing 2 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20180621 MGI PMID:26967477 1317836 Dennd2c DENN domain containing 2C gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 1317836 Dennd2c DENN domain containing 2C gene MP:0011625 cystolithiasis IEA N RGD:5509061 20210128 MGI 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8706134 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20151112 MGI PMID:21679928 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20151112 MGI PMID:21679928 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:8706134 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:8706134 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:8706134 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20151112 MGI PMID:21679928 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20141003 MGI PMID:9712664 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:9712664 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20151112 MGI PMID:21679928 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0002068 abnormal parental behavior IAGP N RGD:5509061 20141003 MGI PMID:8706134 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20151112 MGI PMID:21679928 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0003068 enlarged kidney IEA N RGD:5509061 20181227 MGI 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0003194 abnormal frequency of paradoxical sleep IAGP N RGD:5509061 20141003 MGI PMID:11039731 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20151112 MGI PMID:21679928 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20151112 MGI PMID:21679928 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:8668344 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20151112 MGI PMID:21679928 1317838 Fosb FBJ osteosarcoma oncogene B gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:21679928 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15569927 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:17868091 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:16239343 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:16239343 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20180301 MGI PMID:28483978 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16239343 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:16239343 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0000856 abnormal cerebellar plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16239343 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:15569927 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15569927 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20180301 MGI PMID:28483978 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15870281 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:15569927 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15569927 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15870281 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:15569927 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16239343 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20180301 MGI PMID:28483978 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20180301 MGI PMID:28483978 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20180301 MGI PMID:28483978 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15870281 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15870281 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16239343 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20180301 MGI PMID:28483978 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15569927 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16239343 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11447289 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15870281 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17868091 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15870281 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:15870281 1317843 Frs2 fibroblast growth factor receptor substrate 2 gene MP:0030250 frontonasal prominence hypoplasia IAGP N RGD:5509061 20180301 MGI PMID:28483978 1317847 Etnk1 ethanolamine kinase 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20201022 MGI 1317847 Etnk1 ethanolamine kinase 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1317851 Iars1 isoleucyl-tRNA synthetase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20231109 MGI PMID:37108118 1317851 Iars1 isoleucyl-tRNA synthetase 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20231109 MGI PMID:37108118 1317851 Iars1 isoleucyl-tRNA synthetase 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20231109 MGI PMID:37108118 1317851 Iars1 isoleucyl-tRNA synthetase 1 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20231109 MGI PMID:37108118 1317852 Dnajb6 DnaJ heat shock protein family (Hsp40) member B6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10021343 1317852 Dnajb6 DnaJ heat shock protein family (Hsp40) member B6 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10021343 1317852 Dnajb6 DnaJ heat shock protein family (Hsp40) member B6 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10021343 1317852 Dnajb6 DnaJ heat shock protein family (Hsp40) member B6 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:10021343 1317852 Dnajb6 DnaJ heat shock protein family (Hsp40) member B6 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:10021343 1317852 Dnajb6 DnaJ heat shock protein family (Hsp40) member B6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10021343 1317856 Abhd17c abhydrolase domain containing 17C gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1317856 Abhd17c abhydrolase domain containing 17C gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1317856 Abhd17c abhydrolase domain containing 17C gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 1317856 Abhd17c abhydrolase domain containing 17C gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1317856 Abhd17c abhydrolase domain containing 17C gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1317856 Abhd17c abhydrolase domain containing 17C gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1317856 Abhd17c abhydrolase domain containing 17C gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1317856 Abhd17c abhydrolase domain containing 17C gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1317856 Abhd17c abhydrolase domain containing 17C gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1317856 Abhd17c abhydrolase domain containing 17C gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1317856 Abhd17c abhydrolase domain containing 17C gene MP:0002188 small heart IEA N RGD:5509061 20210826 MGI 1317856 Abhd17c abhydrolase domain containing 17C gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1317856 Abhd17c abhydrolase domain containing 17C gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1317856 Abhd17c abhydrolase domain containing 17C gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 1317856 Abhd17c abhydrolase domain containing 17C gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20210826 MGI 1317858 Klhdc1 kelch domain containing 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20230601 MGI 1317862 Chst12 carbohydrate sulfotransferase 12 gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 1317862 Chst12 carbohydrate sulfotransferase 12 gene MP:0004692 small pubis IAGP N RGD:5509061 20210930 MGI PMID:33905568 1317867 Ess2 ess-2 splicing factor gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20231130 MGI PMID:35933014 1317867 Ess2 ess-2 splicing factor gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20231130 MGI PMID:35933014 1317867 Ess2 ess-2 splicing factor gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20231130 MGI PMID:35933014 1317867 Ess2 ess-2 splicing factor gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20231130 MGI PMID:35933014 1317867 Ess2 ess-2 splicing factor gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20231130 MGI PMID:35933014 1317867 Ess2 ess-2 splicing factor gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20231130 MGI PMID:35933014 1317867 Ess2 ess-2 splicing factor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20231130 MGI PMID:35933014 1317867 Ess2 ess-2 splicing factor gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IAGP N RGD:5509061 20231130 MGI PMID:35933014 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240627 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0001785 edema IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20150903 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1317869 Zmym2 zinc finger, MYM-type 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20230119 MGI 1317875 Rad9b RAD9 checkpoint clamp component B gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:20842695 1317875 Rad9b RAD9 checkpoint clamp component B gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20842695 1317875 Rad9b RAD9 checkpoint clamp component B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20842695 1317875 Rad9b RAD9 checkpoint clamp component B gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:20842695 1317875 Rad9b RAD9 checkpoint clamp component B gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:20842695 1317875 Rad9b RAD9 checkpoint clamp component B gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:20842695 1317875 Rad9b RAD9 checkpoint clamp component B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20842695 1317875 Rad9b RAD9 checkpoint clamp component B gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20842695 1317875 Rad9b RAD9 checkpoint clamp component B gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:20842695 1317875 Rad9b RAD9 checkpoint clamp component B gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:20842695 1317875 Rad9b RAD9 checkpoint clamp component B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20842695 1317875 Rad9b RAD9 checkpoint clamp component B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20842695 1317875 Rad9b RAD9 checkpoint clamp component B gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20842695 1317875 Rad9b RAD9 checkpoint clamp component B gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20842695 1317877 Rag1 recombination activating 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20170209 MGI PMID:17218256 1317877 Rag1 recombination activating 1 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20170209 MGI PMID:17611620 1317877 Rag1 recombination activating 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20220519 MGI PMID:29178458 1317877 Rag1 recombination activating 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20170209 MGI PMID:19109567 1317877 Rag1 recombination activating 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:18563383 1317877 Rag1 recombination activating 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20170209 MGI PMID:16272283 1317877 Rag1 recombination activating 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170209 MGI PMID:16751419 1317877 Rag1 recombination activating 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20170209 MGI PMID:18563383 1317877 Rag1 recombination activating 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20170209 MGI PMID:17681821 1317877 Rag1 recombination activating 1 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20170209 MGI PMID:22773809 1317877 Rag1 recombination activating 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20170209 MGI PMID:18785974 1317877 Rag1 recombination activating 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20240627 MGI PMID:38438357 1317877 Rag1 recombination activating 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:1547488 1317877 Rag1 recombination activating 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20170209 MGI PMID:18785974 1317877 Rag1 recombination activating 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20170209 MGI PMID:16804066 1317877 Rag1 recombination activating 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20170209 MGI PMID:22770884 1317877 Rag1 recombination activating 1 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20170209 MGI PMID:17442925 1317877 Rag1 recombination activating 1 gene MP:0000726 absent lymphocyte IAGP N RGD:5509061 20170209 MGI PMID:14645513 1317877 Rag1 recombination activating 1 gene MP:0000726 absent lymphocyte IAGP N RGD:5509061 20170209 MGI PMID:23995678 1317877 Rag1 recombination activating 1 gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20170209 MGI PMID:10632602 1317877 Rag1 recombination activating 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20170209 MGI PMID:10632602 1317877 Rag1 recombination activating 1 gene MP:0001190 reddish skin IAGP N RGD:5509061 20170209 MGI PMID:19501000 1317877 Rag1 recombination activating 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20170209 MGI PMID:16880407 1317877 Rag1 recombination activating 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20170209 MGI PMID:19501000 1317877 Rag1 recombination activating 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20170209 MGI PMID:15845450 1317877 Rag1 recombination activating 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20170209 MGI PMID:16880407 1317877 Rag1 recombination activating 1 gene MP:0001200 thick skin IAGP N RGD:5509061 20170209 MGI PMID:16880407 1317877 Rag1 recombination activating 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20170209 MGI PMID:24029918 1317877 Rag1 recombination activating 1 gene MP:0001214 skin hyperplasia IAGP N RGD:5509061 20170209 MGI PMID:24029918 1317877 Rag1 recombination activating 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20170209 MGI PMID:16880407 1317877 Rag1 recombination activating 1 gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20170209 MGI PMID:16880407 1317877 Rag1 recombination activating 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220505 MGI PMID:35318366 1317877 Rag1 recombination activating 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240627 MGI PMID:38438357 1317877 Rag1 recombination activating 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20170209 MGI PMID:17681821 1317877 Rag1 recombination activating 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20170209 MGI PMID:18354038 1317877 Rag1 recombination activating 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20240926 MGI PMID:31675497 1317877 Rag1 recombination activating 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20170209 MGI PMID:16751807 1317877 Rag1 recombination activating 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20170209 MGI PMID:16751807 1317877 Rag1 recombination activating 1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20170209 MGI PMID:17611620 1317877 Rag1 recombination activating 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20170209 MGI PMID:18563383 1317877 Rag1 recombination activating 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20170209 MGI PMID:24037376 1317877 Rag1 recombination activating 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:19812384 1317877 Rag1 recombination activating 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20240328 MGI PMID:36037073 1317877 Rag1 recombination activating 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20170209 MGI PMID:22761313 1317877 Rag1 recombination activating 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20170209 MGI PMID:10066708 1317877 Rag1 recombination activating 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20170209 MGI PMID:1547488 1317877 Rag1 recombination activating 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20170209 MGI PMID:22761313 1317877 Rag1 recombination activating 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20171228 MGI PMID:24080084 1317877 Rag1 recombination activating 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:14581608 1317877 Rag1 recombination activating 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:1547488 1317877 Rag1 recombination activating 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:18684012 1317877 Rag1 recombination activating 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20240627 MGI PMID:38438357 1317877 Rag1 recombination activating 1 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:16169499 1317877 Rag1 recombination activating 1 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:18684012 1317877 Rag1 recombination activating 1 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20240328 MGI PMID:36037073 1317877 Rag1 recombination activating 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20170209 MGI PMID:10411922 1317877 Rag1 recombination activating 1 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20170209 MGI PMID:18354038 1317877 Rag1 recombination activating 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20170209 MGI PMID:17218256 1317877 Rag1 recombination activating 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20170209 MGI PMID:22888134 1317877 Rag1 recombination activating 1 gene MP:0001849 ear inflammation IAGP N RGD:5509061 20170209 MGI PMID:16880407 1317877 Rag1 recombination activating 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20170209 MGI PMID:16751419 1317877 Rag1 recombination activating 1 gene MP:0001856 myocarditis IAGP N RGD:5509061 20170209 MGI PMID:14764740 1317877 Rag1 recombination activating 1 gene MP:0001856 myocarditis IAGP N RGD:5509061 20170209 MGI PMID:16751419 1317877 Rag1 recombination activating 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20170209 MGI PMID:17062753 1317877 Rag1 recombination activating 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20170209 MGI PMID:17681821 1317877 Rag1 recombination activating 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20220505 MGI PMID:35318366 1317877 Rag1 recombination activating 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20170209 MGI PMID:15289505 1317877 Rag1 recombination activating 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20170209 MGI PMID:15545995 1317877 Rag1 recombination activating 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20170209 MGI PMID:19590497 1317877 Rag1 recombination activating 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20240627 MGI PMID:38438357 1317877 Rag1 recombination activating 1 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20170209 MGI PMID:16272283 1317877 Rag1 recombination activating 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20170209 MGI PMID:16751807 1317877 Rag1 recombination activating 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20170209 MGI PMID:15782166 1317877 Rag1 recombination activating 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20170209 MGI PMID:16751807 1317877 Rag1 recombination activating 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20170209 MGI PMID:9584189 1317877 Rag1 recombination activating 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20170209 MGI PMID:15782166 1317877 Rag1 recombination activating 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20170209 MGI PMID:16751807 1317877 Rag1 recombination activating 1 gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20170209 MGI PMID:16751807 1317877 Rag1 recombination activating 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20170209 MGI PMID:18354038 1317877 Rag1 recombination activating 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20170209 MGI PMID:18563383 1317877 Rag1 recombination activating 1 gene MP:0002083 premature death IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0002083 premature death IAGP N RGD:5509061 20170209 MGI PMID:16751807 1317877 Rag1 recombination activating 1 gene MP:0002083 premature death IAGP N RGD:5509061 20170209 MGI PMID:17062753 1317877 Rag1 recombination activating 1 gene MP:0002083 premature death IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0002083 premature death IAGP N RGD:5509061 20170209 MGI PMID:9584189 1317877 Rag1 recombination activating 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20170209 MGI PMID:18354038 1317877 Rag1 recombination activating 1 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20170209 MGI PMID:18354038 1317877 Rag1 recombination activating 1 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20170209 MGI PMID:16272283 1317877 Rag1 recombination activating 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20170209 MGI PMID:17062753 1317877 Rag1 recombination activating 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:14581608 1317877 Rag1 recombination activating 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:1547488 1317877 Rag1 recombination activating 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:11313471 1317877 Rag1 recombination activating 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:11696599 1317877 Rag1 recombination activating 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:14581608 1317877 Rag1 recombination activating 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:1547488 1317877 Rag1 recombination activating 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:18187659 1317877 Rag1 recombination activating 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:8934569 1317877 Rag1 recombination activating 1 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20170209 MGI PMID:18354038 1317877 Rag1 recombination activating 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170209 MGI PMID:15780990 1317877 Rag1 recombination activating 1 gene MP:0002343 abnormal lymph node cortex morphology IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0002353 abnormal inguinal lymph node morphology IAGP N RGD:5509061 20170209 MGI PMID:1547488 1317877 Rag1 recombination activating 1 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20170209 MGI PMID:11696599 1317877 Rag1 recombination activating 1 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20170209 MGI PMID:22773809 1317877 Rag1 recombination activating 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20170209 MGI PMID:14645513 1317877 Rag1 recombination activating 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20170209 MGI PMID:15831701 1317877 Rag1 recombination activating 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20170209 MGI PMID:15021880 1317877 Rag1 recombination activating 1 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20170209 MGI PMID:7520000 1317877 Rag1 recombination activating 1 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20170209 MGI PMID:15021880 1317877 Rag1 recombination activating 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20170209 MGI PMID:19109567 1317877 Rag1 recombination activating 1 gene MP:0002415 abnormal neutrophil differentiation IAGP N RGD:5509061 20170209 MGI PMID:19109567 1317877 Rag1 recombination activating 1 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20170209 MGI PMID:18785974 1317877 Rag1 recombination activating 1 gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20170209 MGI PMID:18785974 1317877 Rag1 recombination activating 1 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20170209 MGI PMID:17526724 1317877 Rag1 recombination activating 1 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20170209 MGI PMID:10762410 1317877 Rag1 recombination activating 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20171228 MGI PMID:24080084 1317877 Rag1 recombination activating 1 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20170209 MGI PMID:16880407 1317877 Rag1 recombination activating 1 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20170209 MGI PMID:11696599 1317877 Rag1 recombination activating 1 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20170209 MGI PMID:11696599 1317877 Rag1 recombination activating 1 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20170209 MGI PMID:15845450 1317877 Rag1 recombination activating 1 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20170209 MGI PMID:17062753 1317877 Rag1 recombination activating 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20170209 MGI PMID:17062753 1317877 Rag1 recombination activating 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20170209 MGI PMID:10632602 1317877 Rag1 recombination activating 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20170209 MGI PMID:17062753 1317877 Rag1 recombination activating 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20170209 MGI PMID:17681821 1317877 Rag1 recombination activating 1 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20170209 MGI PMID:17611620 1317877 Rag1 recombination activating 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20170209 MGI PMID:10066708 1317877 Rag1 recombination activating 1 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:18563383 1317877 Rag1 recombination activating 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20170209 MGI PMID:17062753 1317877 Rag1 recombination activating 1 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20220505 MGI PMID:35318366 1317877 Rag1 recombination activating 1 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20170209 MGI PMID:10204494 1317877 Rag1 recombination activating 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20170209 MGI PMID:16751807 1317877 Rag1 recombination activating 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20170209 MGI PMID:16804066 1317877 Rag1 recombination activating 1 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20170209 MGI PMID:15845450 1317877 Rag1 recombination activating 1 gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20170209 MGI PMID:10204494 1317877 Rag1 recombination activating 1 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20170209 MGI PMID:16751807 1317877 Rag1 recombination activating 1 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20170209 MGI PMID:25711213 1317877 Rag1 recombination activating 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20170209 MGI PMID:16751419 1317877 Rag1 recombination activating 1 gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20170209 MGI PMID:10632602 1317877 Rag1 recombination activating 1 gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20170209 MGI PMID:18187659 1317877 Rag1 recombination activating 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20170209 MGI PMID:10632602 1317877 Rag1 recombination activating 1 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20170209 MGI PMID:17681821 1317877 Rag1 recombination activating 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20170209 MGI PMID:18785974 1317877 Rag1 recombination activating 1 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20170209 MGI PMID:16751419 1317877 Rag1 recombination activating 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20170209 MGI PMID:18187659 1317877 Rag1 recombination activating 1 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0004031 insulitis IAGP N RGD:5509061 20170209 MGI PMID:16804066 1317877 Rag1 recombination activating 1 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20170209 MGI PMID:17062753 1317877 Rag1 recombination activating 1 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20170209 MGI PMID:12498815 1317877 Rag1 recombination activating 1 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20170209 MGI PMID:16804066 1317877 Rag1 recombination activating 1 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20170209 MGI PMID:16804066 1317877 Rag1 recombination activating 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20170209 MGI PMID:22761313 1317877 Rag1 recombination activating 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20170209 MGI PMID:16397132 1317877 Rag1 recombination activating 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20170209 MGI PMID:19109567 1317877 Rag1 recombination activating 1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20170209 MGI PMID:16804066 1317877 Rag1 recombination activating 1 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1317877 Rag1 recombination activating 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20220519 MGI PMID:29178458 1317877 Rag1 recombination activating 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20220519 MGI PMID:29178458 1317877 Rag1 recombination activating 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20170209 MGI PMID:16880407 1317877 Rag1 recombination activating 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:15782166 1317877 Rag1 recombination activating 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:16804066 1317877 Rag1 recombination activating 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:17526724 1317877 Rag1 recombination activating 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170209 MGI PMID:14581608 1317877 Rag1 recombination activating 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170209 MGI PMID:22761313 1317877 Rag1 recombination activating 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20170209 MGI PMID:15021880 1317877 Rag1 recombination activating 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20170209 MGI PMID:19285438 1317877 Rag1 recombination activating 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20170209 MGI PMID:22761313 1317877 Rag1 recombination activating 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20170209 MGI PMID:8934569 1317877 Rag1 recombination activating 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20170209 MGI PMID:16272283 1317877 Rag1 recombination activating 1 gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20170209 MGI PMID:17579183 1317877 Rag1 recombination activating 1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20170209 MGI PMID:14581608 1317877 Rag1 recombination activating 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20170209 MGI PMID:16804066 1317877 Rag1 recombination activating 1 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20170209 MGI PMID:17442925 1317877 Rag1 recombination activating 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20170209 MGI PMID:18684012 1317877 Rag1 recombination activating 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20171228 MGI PMID:24080084 1317877 Rag1 recombination activating 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20240627 MGI PMID:38438357 1317877 Rag1 recombination activating 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20170209 MGI PMID:18563383 1317877 Rag1 recombination activating 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20220505 MGI PMID:35318366 1317877 Rag1 recombination activating 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20220505 MGI PMID:35318366 1317877 Rag1 recombination activating 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20170209 MGI PMID:10411922 1317877 Rag1 recombination activating 1 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20190613 MGI PMID:7520367 1317877 Rag1 recombination activating 1 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20170209 MGI PMID:10632602 1317877 Rag1 recombination activating 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20170209 MGI PMID:18563383 1317877 Rag1 recombination activating 1 gene MP:0005434 absent late pro-B cells IEA N RGD:5509061 20170209 MGI 1317877 Rag1 recombination activating 1 gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20220505 MGI PMID:35318366 1317877 Rag1 recombination activating 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20170209 MGI PMID:15308121 1317877 Rag1 recombination activating 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20170209 MGI PMID:16804066 1317877 Rag1 recombination activating 1 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20170209 MGI PMID:17611620 1317877 Rag1 recombination activating 1 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20170209 MGI PMID:14764740 1317877 Rag1 recombination activating 1 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20170209 MGI PMID:15308121 1317877 Rag1 recombination activating 1 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20170209 MGI PMID:16751419 1317877 Rag1 recombination activating 1 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20170209 MGI PMID:18785974 1317877 Rag1 recombination activating 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20170209 MGI PMID:16751807 1317877 Rag1 recombination activating 1 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20170209 MGI PMID:18684012 1317877 Rag1 recombination activating 1 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20170209 MGI PMID:15021880 1317877 Rag1 recombination activating 1 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20170209 MGI PMID:1547488 1317877 Rag1 recombination activating 1 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20200910 MGI PMID:30111894 1317877 Rag1 recombination activating 1 gene MP:0008041 absent NK T cells IAGP N RGD:5509061 20170209 MGI PMID:18785974 1317877 Rag1 recombination activating 1 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0008070 absent T cells IAGP N RGD:5509061 20170209 MGI PMID:18563383 1317877 Rag1 recombination activating 1 gene MP:0008070 absent T cells IAGP N RGD:5509061 20170209 MGI PMID:19501000 1317877 Rag1 recombination activating 1 gene MP:0008070 absent T cells IAGP N RGD:5509061 20240328 MGI PMID:36037073 1317877 Rag1 recombination activating 1 gene MP:0008071 absent B cells IAGP N RGD:5509061 20170209 MGI PMID:19501000 1317877 Rag1 recombination activating 1 gene MP:0008071 absent B cells IAGP N RGD:5509061 20240328 MGI PMID:36037073 1317877 Rag1 recombination activating 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20170209 MGI PMID:10762410 1317877 Rag1 recombination activating 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20170209 MGI PMID:16169499 1317877 Rag1 recombination activating 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20170209 MGI PMID:16804066 1317877 Rag1 recombination activating 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:15345221 1317877 Rag1 recombination activating 1 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:25343476 1317877 Rag1 recombination activating 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20170209 MGI PMID:10762410 1317877 Rag1 recombination activating 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20170209 MGI PMID:18187659 1317877 Rag1 recombination activating 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20190404 MGI 1317877 Rag1 recombination activating 1 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20171228 MGI PMID:24080084 1317877 Rag1 recombination activating 1 gene MP:0008164 abnormal B-1a B cell morphology IAGP N RGD:5509061 20171228 MGI PMID:24080084 1317877 Rag1 recombination activating 1 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20171228 MGI PMID:24080084 1317877 Rag1 recombination activating 1 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20170209 MGI PMID:1547488 1317877 Rag1 recombination activating 1 gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20170209 MGI PMID:18563383 1317877 Rag1 recombination activating 1 gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0008213 absent immature B cells IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20170209 MGI PMID:14557749 1317877 Rag1 recombination activating 1 gene MP:0008244 abnormal peritoneal macrophage morphology IAGP N RGD:5509061 20200910 MGI PMID:30111894 1317877 Rag1 recombination activating 1 gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20170209 MGI PMID:22770884 1317877 Rag1 recombination activating 1 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20170209 MGI PMID:22770884 1317877 Rag1 recombination activating 1 gene MP:0008348 absent gamma-delta T cells IAGP N RGD:5509061 20170209 MGI PMID:22770884 1317877 Rag1 recombination activating 1 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20170209 MGI PMID:17218256 1317877 Rag1 recombination activating 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20170209 MGI PMID:19501000 1317877 Rag1 recombination activating 1 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20171228 MGI PMID:24080084 1317877 Rag1 recombination activating 1 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20170209 MGI PMID:22550081 1317877 Rag1 recombination activating 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20170209 MGI PMID:17218256 1317877 Rag1 recombination activating 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20170209 MGI PMID:15345221 1317877 Rag1 recombination activating 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20170209 MGI PMID:25711213 1317877 Rag1 recombination activating 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20170209 MGI PMID:15345221 1317877 Rag1 recombination activating 1 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20170209 MGI PMID:10411922 1317877 Rag1 recombination activating 1 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20170209 MGI PMID:15345221 1317877 Rag1 recombination activating 1 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20170209 MGI PMID:15345221 1317877 Rag1 recombination activating 1 gene MP:0008711 increased interleukin-9 secretion IAGP N RGD:5509061 20170209 MGI PMID:21600797 1317877 Rag1 recombination activating 1 gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20170209 MGI PMID:1547488 1317877 Rag1 recombination activating 1 gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20170209 MGI PMID:9584189 1317877 Rag1 recombination activating 1 gene MP:0008755 abnormal immunoglobulin V(D)J recombination IAGP N RGD:5509061 20170209 MGI PMID:10586023 1317877 Rag1 recombination activating 1 gene MP:0008755 abnormal immunoglobulin V(D)J recombination IAGP N RGD:5509061 20170209 MGI PMID:1547488 1317877 Rag1 recombination activating 1 gene MP:0008758 abnormal T cell receptor beta chain V(D)J recombination IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20170209 MGI PMID:19126872 1317877 Rag1 recombination activating 1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20170209 MGI PMID:10419884 1317877 Rag1 recombination activating 1 gene MP:0008925 increased cerebellar granule cell number IAGP N RGD:5509061 20170209 MGI PMID:16751807 1317877 Rag1 recombination activating 1 gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20170209 MGI PMID:17579183 1317877 Rag1 recombination activating 1 gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20170209 MGI PMID:17502664 1317877 Rag1 recombination activating 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20170209 MGI PMID:17579183 1317877 Rag1 recombination activating 1 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20170209 MGI PMID:19109567 1317877 Rag1 recombination activating 1 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20170209 MGI PMID:21179499 1317877 Rag1 recombination activating 1 gene MP:0010250 absent thymus cortex IAGP N RGD:5509061 20170209 MGI PMID:18785974 1317877 Rag1 recombination activating 1 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20170209 MGI PMID:16751807 1317877 Rag1 recombination activating 1 gene MP:0010742 increased Schwann cell number IAGP N RGD:5509061 20170209 MGI PMID:10632602 1317877 Rag1 recombination activating 1 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20190404 MGI 1317877 Rag1 recombination activating 1 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20170209 MGI PMID:17611620 1317877 Rag1 recombination activating 1 gene MP:0010932 increased trabecular bone connectivity density IAGP N RGD:5509061 20170209 MGI PMID:17611620 1317877 Rag1 recombination activating 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:18563383 1317877 Rag1 recombination activating 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:19501000 1317877 Rag1 recombination activating 1 gene MP:0011310 abnormal kidney capillary morphology IAGP N RGD:5509061 20220505 MGI PMID:35318366 1317877 Rag1 recombination activating 1 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20220505 MGI PMID:35318366 1317877 Rag1 recombination activating 1 gene MP:0011370 increased mesangial cell apoptosis IAGP N RGD:5509061 20170209 MGI PMID:17681821 1317877 Rag1 recombination activating 1 gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20220505 MGI PMID:35318366 1317877 Rag1 recombination activating 1 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20220505 MGI PMID:35318366 1317877 Rag1 recombination activating 1 gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20220505 MGI PMID:35318366 1317877 Rag1 recombination activating 1 gene MP:0012563 increased tumor incidence following infection IAGP N RGD:5509061 20241114 MGI PMID:36103821 1317877 Rag1 recombination activating 1 gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20190404 MGI 1317877 Rag1 recombination activating 1 gene MP:0013147 limb paralysis IAGP N RGD:5509061 20190613 MGI PMID:7520367 1317877 Rag1 recombination activating 1 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20190404 MGI 1317877 Rag1 recombination activating 1 gene MP:0013587 absent thymus medulla IAGP N RGD:5509061 20170209 MGI PMID:18785974 1317877 Rag1 recombination activating 1 gene MP:0014130 thymus cyst IAGP N RGD:5509061 20170209 MGI PMID:18785974 1317877 Rag1 recombination activating 1 gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:18785974 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0001925 male infertility IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0009231 detached acrosome IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20180809 MGI PMID:25781171 1317880 Lrguk leucine-rich repeats and guanylate kinase domain containing gene MP:0031373 abnormal manchette perinuclear ring morphology IAGP N RGD:5509061 20220407 MGI PMID:25781171 1317889 Akr1c12 aldo-keto reductase family 1, member C12 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1317891 Carns1 carnosine synthase 1 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20210114 MGI PMID:33040025 1317891 Carns1 carnosine synthase 1 gene MP:0020348 decreased olfactory sensory neuron number IAGP N RGD:5509061 20210114 MGI PMID:33040025 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20191010 MGI PMID:29337306 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20240125 MGI PMID:36056013 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20231102 MGI PMID:35784893 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0001596 hypotension IAGP N RGD:5509061 20231102 MGI PMID:35784893 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20231102 MGI PMID:35784893 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20231102 MGI PMID:35784893 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0001785 edema IAGP N RGD:5509061 20191010 MGI PMID:29337306 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20231102 MGI PMID:35784893 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20191010 MGI PMID:29337306 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20231102 MGI PMID:35784893 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20191010 MGI PMID:29337306 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20191010 MGI PMID:29337306 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20231102 MGI PMID:35784893 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20231102 MGI PMID:35784893 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20231102 MGI PMID:35784893 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0009617 decreased brain zinc level IAGP N RGD:5509061 20240125 MGI PMID:36056013 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20191010 MGI PMID:29337306 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20191010 MGI PMID:29337306 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0011394 increased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20191010 MGI PMID:29337306 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20240125 MGI PMID:36056013 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0020893 abnormal zinc level IAGP N RGD:5509061 20191010 MGI PMID:29337306 1317895 Slc39a8 solute carrier family 39 (metal ion transporter), member 8 gene MP:0031173 increased circulating zinc level IAGP N RGD:5509061 20240125 MGI PMID:36056013 1317897 Rorc RAR-related orphan receptor gamma gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:20226692 1317897 Rorc RAR-related orphan receptor gamma gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10963675 1317897 Rorc RAR-related orphan receptor gamma gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20180301 MGI PMID:28846085 1317897 Rorc RAR-related orphan receptor gamma gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14691482 1317897 Rorc RAR-related orphan receptor gamma gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20226692 1317897 Rorc RAR-related orphan receptor gamma gene MP:0001652 colonic necrosis IAGP N RGD:5509061 20141003 MGI PMID:20226692 1317897 Rorc RAR-related orphan receptor gamma gene MP:0001805 decreased IgG level IEA N RGD:5509061 20160915 MGI 1317897 Rorc RAR-related orphan receptor gamma gene MP:0001806 decreased IgM level IEA N RGD:5509061 20150305 MGI 1317897 Rorc RAR-related orphan receptor gamma gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10963675 1317897 Rorc RAR-related orphan receptor gamma gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17882258 1317897 Rorc RAR-related orphan receptor gamma gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20180301 MGI PMID:28846085 1317897 Rorc RAR-related orphan receptor gamma gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:14691482 1317897 Rorc RAR-related orphan receptor gamma gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15247480 1317897 Rorc RAR-related orphan receptor gamma gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20226692 1317897 Rorc RAR-related orphan receptor gamma gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IEA N RGD:5509061 20160915 MGI 1317897 Rorc RAR-related orphan receptor gamma gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10963675 1317897 Rorc RAR-related orphan receptor gamma gene MP:0002450 abnormal lymph organ development IAGP N RGD:5509061 20141003 MGI PMID:10963675 1317897 Rorc RAR-related orphan receptor gamma gene MP:0002450 abnormal lymph organ development IAGP N RGD:5509061 20141003 MGI PMID:14691482 1317897 Rorc RAR-related orphan receptor gamma gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:20226692 1317897 Rorc RAR-related orphan receptor gamma gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:10963675 1317897 Rorc RAR-related orphan receptor gamma gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:14691482 1317897 Rorc RAR-related orphan receptor gamma gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20180301 MGI PMID:28846085 1317897 Rorc RAR-related orphan receptor gamma gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20180301 MGI PMID:28846085 1317897 Rorc RAR-related orphan receptor gamma gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180301 MGI PMID:28846085 1317897 Rorc RAR-related orphan receptor gamma gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:10963675 1317897 Rorc RAR-related orphan receptor gamma gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10963675 1317897 Rorc RAR-related orphan receptor gamma gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:15247480 1317897 Rorc RAR-related orphan receptor gamma gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:10963675 1317897 Rorc RAR-related orphan receptor gamma gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10963675 1317897 Rorc RAR-related orphan receptor gamma gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14691482 1317897 Rorc RAR-related orphan receptor gamma gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20180301 MGI PMID:28846085 1317897 Rorc RAR-related orphan receptor gamma gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10963675 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10963675 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:14691482 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20180301 MGI PMID:28846085 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20180301 MGI PMID:28846085 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19084435 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10963675 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180301 MGI PMID:28846085 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20160915 MGI 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10963675 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20180301 MGI PMID:28846085 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008167 increased B-1a cell number IEA N RGD:5509061 20160915 MGI 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20160915 MGI 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20160915 MGI 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008400 abnormal CD4-positive, alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15247480 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008401 abnormal CD8 positive, alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15247480 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:17581589 1317897 Rorc RAR-related orphan receptor gamma gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:10963675 1317897 Rorc RAR-related orphan receptor gamma gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14691482 1317897 Rorc RAR-related orphan receptor gamma gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20180301 MGI PMID:28846085 1317897 Rorc RAR-related orphan receptor gamma gene MP:0009624 small inguinal lymph nodes IAGP N RGD:5509061 20180301 MGI PMID:28846085 1317897 Rorc RAR-related orphan receptor gamma gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20226692 1317897 Rorc RAR-related orphan receptor gamma gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20180301 MGI PMID:28846085 1317897 Rorc RAR-related orphan receptor gamma gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20160915 MGI 1317897 Rorc RAR-related orphan receptor gamma gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20160915 MGI 1317897 Rorc RAR-related orphan receptor gamma gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20160915 MGI 1317897 Rorc RAR-related orphan receptor gamma gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20150305 MGI 1317897 Rorc RAR-related orphan receptor gamma gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20150305 MGI 1317899 Cd209a CD209a antigen gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1317899 Cd209a CD209a antigen gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20150226 MGI PMID:23118208 1317899 Cd209a CD209a antigen gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:23254286 1317899 Cd209a CD209a antigen gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1317899 Cd209a CD209a antigen gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20150226 MGI PMID:23118208 1317899 Cd209a CD209a antigen gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1317899 Cd209a CD209a antigen gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1317899 Cd209a CD209a antigen gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1317899 Cd209a CD209a antigen gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20150226 MGI PMID:23118208 1317899 Cd209a CD209a antigen gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1317899 Cd209a CD209a antigen gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23254286 1317905 Tomm7 translocase of outer mitochondrial membrane 7 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20210513 MGI PMID:30354240 1317905 Tomm7 translocase of outer mitochondrial membrane 7 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20210513 MGI PMID:30354240 1317905 Tomm7 translocase of outer mitochondrial membrane 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210513 MGI PMID:30354240 1317905 Tomm7 translocase of outer mitochondrial membrane 7 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20210513 MGI PMID:30354240 1317905 Tomm7 translocase of outer mitochondrial membrane 7 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20210513 MGI PMID:30354240 1317905 Tomm7 translocase of outer mitochondrial membrane 7 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20210513 MGI PMID:30354240 1317910 Coq8a coenzyme Q8A gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20190926 MGI PMID:27499294 1317910 Coq8a coenzyme Q8A gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20190926 MGI PMID:27499294 1317910 Coq8a coenzyme Q8A gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20190926 MGI PMID:27499294 1317910 Coq8a coenzyme Q8A gene MP:0001393 ataxia IAGP N RGD:5509061 20190926 MGI PMID:27499294 1317910 Coq8a coenzyme Q8A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190926 MGI PMID:27499294 1317910 Coq8a coenzyme Q8A gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20190926 MGI PMID:27499294 1317910 Coq8a coenzyme Q8A gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20190926 MGI PMID:27499294 1317910 Coq8a coenzyme Q8A gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20190926 MGI PMID:27499294 1317910 Coq8a coenzyme Q8A gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20190926 MGI PMID:27499294 1317910 Coq8a coenzyme Q8A gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20190926 MGI PMID:27499294 1317910 Coq8a coenzyme Q8A gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20190926 MGI PMID:27499294 1317910 Coq8a coenzyme Q8A gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20190926 MGI PMID:27499294 1317910 Coq8a coenzyme Q8A gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20190926 MGI PMID:27499294 1317911 Ms4a4d membrane-spanning 4-domains, subfamily A, member 4D gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1317911 Ms4a4d membrane-spanning 4-domains, subfamily A, member 4D gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240627 MGI 1317911 Ms4a4d membrane-spanning 4-domains, subfamily A, member 4D gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1317913 Polm polymerase (DNA directed), mu gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:12932354 1317913 Polm polymerase (DNA directed), mu gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16860755 1317913 Polm polymerase (DNA directed), mu gene MP:0002223 lymphoid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12932354 1317913 Polm polymerase (DNA directed), mu gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:15789338 1317913 Polm polymerase (DNA directed), mu gene MP:0002619 abnormal lymphocyte morphology IEA N RGD:5509061 20190418 MGI 1317913 Polm polymerase (DNA directed), mu gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11937519 1317913 Polm polymerase (DNA directed), mu gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12932354 1317913 Polm polymerase (DNA directed), mu gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16860755 1317913 Polm polymerase (DNA directed), mu gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12932354 1317913 Polm polymerase (DNA directed), mu gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:16860755 1317913 Polm polymerase (DNA directed), mu gene MP:0008761 abnormal immunoglobulin light chain V-J recombination IAGP N RGD:5509061 20141003 MGI PMID:16860755 1317915 Pld3 phospholipase D family member 3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200910 MGI PMID:30111894 1317915 Pld3 phospholipase D family member 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200910 MGI PMID:30111894 1317915 Pld3 phospholipase D family member 3 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210128 MGI 1317915 Pld3 phospholipase D family member 3 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20170105 MGI 1317915 Pld3 phospholipase D family member 3 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20200910 MGI PMID:30111894 1317915 Pld3 phospholipase D family member 3 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20200910 MGI PMID:30111894 1317915 Pld3 phospholipase D family member 3 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20200910 MGI PMID:30111894 1317915 Pld3 phospholipase D family member 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20200910 MGI PMID:30111894 1317915 Pld3 phospholipase D family member 3 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20200910 MGI PMID:30111894 1317915 Pld3 phospholipase D family member 3 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200910 MGI PMID:30111894 1317915 Pld3 phospholipase D family member 3 gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20200910 MGI PMID:30111894 1317915 Pld3 phospholipase D family member 3 gene MP:0031070 hemophagocytosis IAGP N RGD:5509061 20200910 MGI PMID:30111894 1317915 Pld3 phospholipase D family member 3 gene MP:0031220 increased circulating CXCL10 level IAGP N RGD:5509061 20210204 MGI PMID:30111894 1317917 Fer1l4 fer-1 like family member 4 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20200402 MGI 1317918 Prxl2b peroxiredoxin like 2B gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20210819 MGI PMID:33418484 1317918 Prxl2b peroxiredoxin like 2B gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20210819 MGI PMID:33418484 1317918 Prxl2b peroxiredoxin like 2B gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1317920 Ffar4 free fatty acid receptor 4 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0001985 abnormal gustatory system physiology IAGP N RGD:5509061 20141003 MGI PMID:20573884 1317920 Ffar4 free fatty acid receptor 4 gene MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20573884 1317920 Ffar4 free fatty acid receptor 4 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20170608 MGI PMID:27853148 1317920 Ffar4 free fatty acid receptor 4 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20160721 MGI PMID:24663807 1317920 Ffar4 free fatty acid receptor 4 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20170608 MGI PMID:27853148 1317920 Ffar4 free fatty acid receptor 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20170608 MGI PMID:27853148 1317920 Ffar4 free fatty acid receptor 4 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20170608 MGI PMID:27853148 1317920 Ffar4 free fatty acid receptor 4 gene MP:0008953 abnormal pancreatic somatostatin secretion IAGP N RGD:5509061 20160721 MGI PMID:24663807 1317920 Ffar4 free fatty acid receptor 4 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0010055 abnormal sensory neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:20573884 1317920 Ffar4 free fatty acid receptor 4 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22343897 1317920 Ffar4 free fatty acid receptor 4 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20170608 MGI PMID:27853148 1317920 Ffar4 free fatty acid receptor 4 gene MP:0011169 abnormal white fat cell differentation IAGP N RGD:5509061 20170608 MGI PMID:27853148 1317920 Ffar4 free fatty acid receptor 4 gene MP:0011170 abnormal brown fat cell differentiation IAGP N RGD:5509061 20170608 MGI PMID:27853148 1317920 Ffar4 free fatty acid receptor 4 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20170608 MGI PMID:27853148 1317920 Ffar4 free fatty acid receptor 4 gene MP:0020426 abnormal beige fat cell physiology IAGP N RGD:5509061 20170803 MGI PMID:27853148 1317922 Bin3 bridging integrator 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18339847 1317922 Bin3 bridging integrator 3 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18339847 1317922 Bin3 bridging integrator 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18339847 1317922 Bin3 bridging integrator 3 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:18339847 1317922 Bin3 bridging integrator 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18339847 1317922 Bin3 bridging integrator 3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18339847 1317922 Bin3 bridging integrator 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18339847 1317922 Bin3 bridging integrator 3 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18339847 1317922 Bin3 bridging integrator 3 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18339847 1317922 Bin3 bridging integrator 3 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:18339847 1317922 Bin3 bridging integrator 3 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18339847 1317923 Ctf2 cardiotrophin 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1317925 Pmepa1 prostate transmembrane protein, androgen induced 1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20231109 MGI PMID:33484199 1317925 Pmepa1 prostate transmembrane protein, androgen induced 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20231109 MGI PMID:33484199 1317925 Pmepa1 prostate transmembrane protein, androgen induced 1 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20231109 MGI PMID:33484199 1317925 Pmepa1 prostate transmembrane protein, androgen induced 1 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20231109 MGI PMID:33484199 1317925 Pmepa1 prostate transmembrane protein, androgen induced 1 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20231109 MGI PMID:33484199 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0008285 abnormal hippocampus granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0009946 abnormal olfactory bulb layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0009951 abnormal olfactory bulb mitral cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0010011 ectopic hippocampus pyramidal cells IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317927 Apc2 APC regulator of WNT signaling pathway 2 gene MP:0010540 long stride length IAGP N RGD:5509061 20141003 MGI PMID:22573669 1317931 Mbd3l1 methyl-CpG binding domain protein 3-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15456747 1317931 Mbd3l1 methyl-CpG binding domain protein 3-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18942147 1317932 Ano10 anoctamin 10 gene MP:0014208 decreased intestinal epithelial chloride transmembrane transport IAGP N RGD:5509061 20180503 MGI PMID:24974903 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:12514127 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11786513 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15870258 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:12514127 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0010502 ventricle myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317935 Myl7 myosin, light polypeptide 7, regulatory gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:14573518 1317937 Adck1 aarF domain containing kinase 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1317939 Tbx21 T-box 21 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18635804 1317939 Tbx21 T-box 21 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17923086 1317939 Tbx21 T-box 21 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:17923086 1317939 Tbx21 T-box 21 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:14744755 1317939 Tbx21 T-box 21 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17923086 1317939 Tbx21 T-box 21 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:18635804 1317939 Tbx21 T-box 21 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15665085 1317939 Tbx21 T-box 21 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:11786643 1317939 Tbx21 T-box 21 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20713880 1317939 Tbx21 T-box 21 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:11786643 1317939 Tbx21 T-box 21 gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:11786643 1317939 Tbx21 T-box 21 gene MP:0002433 abnormal T-helper 1 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16273099 1317939 Tbx21 T-box 21 gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11786644 1317939 Tbx21 T-box 21 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18635804 1317939 Tbx21 T-box 21 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11786644 1317939 Tbx21 T-box 21 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15665085 1317939 Tbx21 T-box 21 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:17923086 1317939 Tbx21 T-box 21 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16827899 1317939 Tbx21 T-box 21 gene MP:0003080 increased natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11786644 1317939 Tbx21 T-box 21 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:20713880 1317939 Tbx21 T-box 21 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:17923086 1317939 Tbx21 T-box 21 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16827899 1317939 Tbx21 T-box 21 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17923086 1317939 Tbx21 T-box 21 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:11786644 1317939 Tbx21 T-box 21 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11786644 1317939 Tbx21 T-box 21 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15665085 1317939 Tbx21 T-box 21 gene MP:0005340 abnormal susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15665085 1317939 Tbx21 T-box 21 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16827899 1317939 Tbx21 T-box 21 gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:16827899 1317939 Tbx21 T-box 21 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18635804 1317939 Tbx21 T-box 21 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:16273099 1317939 Tbx21 T-box 21 gene MP:0008041 absent NK T cells IAGP N RGD:5509061 20141003 MGI PMID:16273099 1317939 Tbx21 T-box 21 gene MP:0008041 absent NK T cells IAGP N RGD:5509061 20141003 MGI PMID:19808259 1317939 Tbx21 T-box 21 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19808259 1317939 Tbx21 T-box 21 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:16273099 1317939 Tbx21 T-box 21 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19808259 1317939 Tbx21 T-box 21 gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16273099 1317939 Tbx21 T-box 21 gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18635804 1317939 Tbx21 T-box 21 gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:20713880 1317939 Tbx21 T-box 21 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19808259 1317939 Tbx21 T-box 21 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20151231 MGI PMID:24516120 1317939 Tbx21 T-box 21 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20713880 1317939 Tbx21 T-box 21 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19119024 1317939 Tbx21 T-box 21 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 1317939 Tbx21 T-box 21 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18635804 1317939 Tbx21 T-box 21 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20713880 1317939 Tbx21 T-box 21 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21623380 1317939 Tbx21 T-box 21 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18635804 1317939 Tbx21 T-box 21 gene MP:0008087 decreased T helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:11786644 1317939 Tbx21 T-box 21 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11786644 1317939 Tbx21 T-box 21 gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:11786644 1317939 Tbx21 T-box 21 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:17923086 1317939 Tbx21 T-box 21 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17923086 1317939 Tbx21 T-box 21 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21623380 1317939 Tbx21 T-box 21 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11786644 1317939 Tbx21 T-box 21 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15665085 1317939 Tbx21 T-box 21 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16273099 1317939 Tbx21 T-box 21 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20713880 1317939 Tbx21 T-box 21 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:24249732 1317939 Tbx21 T-box 21 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:15665085 1317939 Tbx21 T-box 21 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:20713880 1317939 Tbx21 T-box 21 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:21623380 1317939 Tbx21 T-box 21 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:21623380 1317939 Tbx21 T-box 21 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20713880 1317939 Tbx21 T-box 21 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:11786643 1317939 Tbx21 T-box 21 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:11786644 1317939 Tbx21 T-box 21 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:16200068 1317939 Tbx21 T-box 21 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:11786643 1317939 Tbx21 T-box 21 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:18635804 1317939 Tbx21 T-box 21 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:11786643 1317939 Tbx21 T-box 21 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:14744755 1317939 Tbx21 T-box 21 gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14744755 1317939 Tbx21 T-box 21 gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14744755 1317939 Tbx21 T-box 21 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11786644 1317939 Tbx21 T-box 21 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 1317939 Tbx21 T-box 21 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:18635804 1317939 Tbx21 T-box 21 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:21623380 1317945 Rprd2 regulation of nuclear pre-mRNA domain containing 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1317945 Rprd2 regulation of nuclear pre-mRNA domain containing 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1317945 Rprd2 regulation of nuclear pre-mRNA domain containing 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1317945 Rprd2 regulation of nuclear pre-mRNA domain containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317945 Rprd2 regulation of nuclear pre-mRNA domain containing 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1317947 Plek pleckstrin gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19190246 1317947 Plek pleckstrin gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:19190246 1317947 Plek pleckstrin gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:19190246 1317949 Kif1b kinesin family member 1B gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:11389829 1317949 Kif1b kinesin family member 1B gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:11389829 1317949 Kif1b kinesin family member 1B gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:11389829 1317949 Kif1b kinesin family member 1B gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:11389829 1317949 Kif1b kinesin family member 1B gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1317949 Kif1b kinesin family member 1B gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11389829 1317949 Kif1b kinesin family member 1B gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1317949 Kif1b kinesin family member 1B gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1317949 Kif1b kinesin family member 1B gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11389829 1317949 Kif1b kinesin family member 1B gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:11389829 1317949 Kif1b kinesin family member 1B gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1317949 Kif1b kinesin family member 1B gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1317949 Kif1b kinesin family member 1B gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11389829 1317949 Kif1b kinesin family member 1B gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20160811 MGI 1317949 Kif1b kinesin family member 1B gene MP:0002177 abnormal outer ear morphology IEA N RGD:5509061 20160811 MGI 1317949 Kif1b kinesin family member 1B gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:11389829 1317949 Kif1b kinesin family member 1B gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1317949 Kif1b kinesin family member 1B gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20210128 MGI 1317949 Kif1b kinesin family member 1B gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20160811 MGI 1317949 Kif1b kinesin family member 1B gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:11389829 1317949 Kif1b kinesin family member 1B gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:11389829 1317949 Kif1b kinesin family member 1B gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:11389829 1317949 Kif1b kinesin family member 1B gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:11389829 1317949 Kif1b kinesin family member 1B gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1317949 Kif1b kinesin family member 1B gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160421 MGI 1317949 Kif1b kinesin family member 1B gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 1317949 Kif1b kinesin family member 1B gene MP:0008762 embryonic lethality IEA N RGD:5509061 20141106 MGI 1317949 Kif1b kinesin family member 1B gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:11389829 1317949 Kif1b kinesin family member 1B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11389829 1317949 Kif1b kinesin family member 1B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317949 Kif1b kinesin family member 1B gene MP:0011495 abnormal head shape IEA N RGD:5509061 20160811 MGI 1317949 Kif1b kinesin family member 1B gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1317951 Srpk1 serine/arginine-rich protein specific kinase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20191226 MGI PMID:24703948 1317951 Srpk1 serine/arginine-rich protein specific kinase 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20191226 MGI PMID:24703948 1317951 Srpk1 serine/arginine-rich protein specific kinase 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IAGP N RGD:5509061 20191226 MGI PMID:24703948 1317958 Calhm2 calcium homeostasis modulator family member 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210128 MGI 1317958 Calhm2 calcium homeostasis modulator family member 2 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20181227 MGI 1317958 Calhm2 calcium homeostasis modulator family member 2 gene MP:0003450 enlarged pancreas IEA N RGD:5509061 20181227 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0000599 enlarged liver IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0001304 cataract IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0001523 impaired righting response IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1317962 Wars1 tryptophanyl-tRNA synthetase1 gene MP:0011897 decreased circulating unsaturated transferrin level IEA N RGD:5509061 20230601 MGI 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19450229 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:24051378 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19450229 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19706465 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19706465 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0003839 abnormal insulin clearance IAGP N RGD:5509061 20141003 MGI PMID:24051378 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24051378 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19706465 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:24051378 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19706465 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160804 MGI 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19706465 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0009615 abnormal zinc homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19450229 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0009615 abnormal zinc homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19706465 1317969 Slc30a8 solute carrier family 30 (zinc transporter), member 8 gene MP:0009615 abnormal zinc homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24051378 1317973 Stoml2 stomatin (Epb7.2)-like 2 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1317973 Stoml2 stomatin (Epb7.2)-like 2 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20231207 MGI 1317973 Stoml2 stomatin (Epb7.2)-like 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1317973 Stoml2 stomatin (Epb7.2)-like 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1317973 Stoml2 stomatin (Epb7.2)-like 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20231207 MGI 1317973 Stoml2 stomatin (Epb7.2)-like 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200514 MGI 1317978 Lcp1 lymphocyte cytosolic protein 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1317978 Lcp1 lymphocyte cytosolic protein 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12871642 1317978 Lcp1 lymphocyte cytosolic protein 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12871642 1317978 Lcp1 lymphocyte cytosolic protein 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:12871642 1317978 Lcp1 lymphocyte cytosolic protein 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1317978 Lcp1 lymphocyte cytosolic protein 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 1317978 Lcp1 lymphocyte cytosolic protein 1 gene MP:0008652 decreased interleukin-1 secretion IAGP N RGD:5509061 20141003 MGI PMID:12871642 1317978 Lcp1 lymphocyte cytosolic protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1317978 Lcp1 lymphocyte cytosolic protein 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1317983 Nudt15 nudix hydrolase 15 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20240307 MGI PMID:31645647 1317983 Nudt15 nudix hydrolase 15 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20240307 MGI PMID:31645647 1317983 Nudt15 nudix hydrolase 15 gene MP:0002083 premature death IAGP N RGD:5509061 20240307 MGI PMID:31645647 1317983 Nudt15 nudix hydrolase 15 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20240307 MGI PMID:31645647 1317983 Nudt15 nudix hydrolase 15 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20240307 MGI PMID:31645647 1317983 Nudt15 nudix hydrolase 15 gene MP:0014399 decreased hematopoietic precursor cell number IAGP N RGD:5509061 20240321 MGI PMID:31645647 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23785158 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160421 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210520 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:15470499 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210520 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15470499 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23785158 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001376 abnormal mating receptivity IAGP N RGD:5509061 20141003 MGI PMID:15465527 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:12419415 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:12077327 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15465527 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:15465527 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:12077327 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0002059 abnormal seminal vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12419415 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12077327 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210520 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:15465527 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:15470499 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0002716 small male preputial gland IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15470499 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:12419415 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:15470499 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20141003 MGI PMID:12419415 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0003578 absent ovary IEA N RGD:5509061 20210520 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210520 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160421 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0003918 decreased kidney weight IEA N RGD:5509061 20210128 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0003929 decreased heart rate variability IAGP N RGD:5509061 20141003 MGI PMID:12077327 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0004156 abnormal QT variability IAGP N RGD:5509061 20141003 MGI PMID:12077327 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0004727 absent epididymis IEA N RGD:5509061 20210520 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:23785158 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:23785158 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0005188 small penis IAGP N RGD:5509061 20141003 MGI PMID:15470499 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0005188 small penis IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20141003 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20181227 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:12419415 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20220804 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20231207 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0006110 ventricular fibrillation IAGP N RGD:5509061 20141003 MGI PMID:12077327 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0006277 abnormal parasympathetic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12077327 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0006415 absent testes IEA N RGD:5509061 20181227 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23785158 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:15470499 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23785158 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:15465527 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:15465527 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0009014 prolonged proestrus IAGP N RGD:5509061 20141003 MGI PMID:15465527 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0009018 short estrus IAGP N RGD:5509061 20141003 MGI PMID:15465527 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20141003 MGI PMID:12077327 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160421 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:12419415 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20141003 MGI PMID:23785158 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20170202 MGI PMID:23785158 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0031287 bilateral cryptorchism IAGP N RGD:5509061 20211014 MGI PMID:9090387 1317986 Nhlh2 nescient helix loop helix 2 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:15465527 1317988 Nxnl1 nucleoredoxin-like 1 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:20139892 1317988 Nxnl1 nucleoredoxin-like 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20139892 1317988 Nxnl1 nucleoredoxin-like 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20139892 1317988 Nxnl1 nucleoredoxin-like 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20139892 1317988 Nxnl1 nucleoredoxin-like 1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:20139892 1317988 Nxnl1 nucleoredoxin-like 1 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:20139892 1317988 Nxnl1 nucleoredoxin-like 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20139892 1317988 Nxnl1 nucleoredoxin-like 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:20139892 1317991 Mmp25 matrix metallopeptidase 25 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20240704 MGI PMID:27259858 1317991 Mmp25 matrix metallopeptidase 25 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20240704 MGI PMID:27259858 1317991 Mmp25 matrix metallopeptidase 25 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20240704 MGI PMID:38570687 1317991 Mmp25 matrix metallopeptidase 25 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20240704 MGI PMID:38570687 1317991 Mmp25 matrix metallopeptidase 25 gene MP:0008639 decreased circulating interleukin-1 alpha level IAGP N RGD:5509061 20240704 MGI PMID:27259858 1317991 Mmp25 matrix metallopeptidase 25 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20240704 MGI PMID:27259858 1317991 Mmp25 matrix metallopeptidase 25 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20240704 MGI PMID:27259858 1317991 Mmp25 matrix metallopeptidase 25 gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20240704 MGI PMID:27259858 1317994 H3f3a H3.3 histone A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23315948 1317994 H3f3a H3.3 histone A gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:10556297 1317994 H3f3a H3.3 histone A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10556297 1317994 H3f3a H3.3 histone A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10362650 1317994 H3f3a H3.3 histone A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23315948 1317994 H3f3a H3.3 histone A gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10362650 1317994 H3f3a H3.3 histone A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23315948 1317994 H3f3a H3.3 histone A gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10556297 1317996 Rrp8 ribosomal RNA processing 8 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1317996 Rrp8 ribosomal RNA processing 8 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1317996 Rrp8 ribosomal RNA processing 8 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20240523 MGI 1317996 Rrp8 ribosomal RNA processing 8 gene MP:0003064 decreased coping response IEA N RGD:5509061 20210128 MGI 1317996 Rrp8 ribosomal RNA processing 8 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1317996 Rrp8 ribosomal RNA processing 8 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1317996 Rrp8 ribosomal RNA processing 8 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1317998 Atp6v0b ATPase, H+ transporting, lysosomal V0 subunit B gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1317998 Atp6v0b ATPase, H+ transporting, lysosomal V0 subunit B gene MP:0001399 hyperactivity IEA N RGD:5509061 20221215 MGI 1317998 Atp6v0b ATPase, H+ transporting, lysosomal V0 subunit B gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20221215 MGI 1317998 Atp6v0b ATPase, H+ transporting, lysosomal V0 subunit B gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20221215 MGI 1317998 Atp6v0b ATPase, H+ transporting, lysosomal V0 subunit B gene MP:0002608 increased hematocrit IEA N RGD:5509061 20231207 MGI 1317998 Atp6v0b ATPase, H+ transporting, lysosomal V0 subunit B gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1317998 Atp6v0b ATPase, H+ transporting, lysosomal V0 subunit B gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1317998 Atp6v0b ATPase, H+ transporting, lysosomal V0 subunit B gene MP:0004924 abnormal behavior IEA N RGD:5509061 20240523 MGI 1317998 Atp6v0b ATPase, H+ transporting, lysosomal V0 subunit B gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1317998 Atp6v0b ATPase, H+ transporting, lysosomal V0 subunit B gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230601 MGI 1317998 Atp6v0b ATPase, H+ transporting, lysosomal V0 subunit B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1318002 Denr density-regulated protein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1318002 Denr density-regulated protein gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318002 Denr density-regulated protein gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318002 Denr density-regulated protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318002 Denr density-regulated protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318002 Denr density-regulated protein gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1318003 Pdpr pyruvate dehydrogenase phosphatase regulatory subunit gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1318003 Pdpr pyruvate dehydrogenase phosphatase regulatory subunit gene MP:0002608 increased hematocrit IEA N RGD:5509061 20201022 MGI 1318003 Pdpr pyruvate dehydrogenase phosphatase regulatory subunit gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20201022 MGI 1318003 Pdpr pyruvate dehydrogenase phosphatase regulatory subunit gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20181227 MGI 1318003 Pdpr pyruvate dehydrogenase phosphatase regulatory subunit gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1318003 Pdpr pyruvate dehydrogenase phosphatase regulatory subunit gene MP:0012361 decreased large unstained cell number IEA N RGD:5509061 20201022 MGI 1318003 Pdpr pyruvate dehydrogenase phosphatase regulatory subunit gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1318008 Eps8l3 EPS8-like 3 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20181227 MGI 1318008 Eps8l3 EPS8-like 3 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20160421 MGI 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20190131 MGI PMID:28939830 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21600797 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20190131 MGI PMID:28939830 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:21600797 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20210318 MGI PMID:32342103 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16717117 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16546100 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20190131 MGI PMID:28939830 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20190131 MGI PMID:28939830 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16407890 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20190131 MGI PMID:28939830 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20151224 MGI PMID:26642356 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200130 MGI PMID:30662948 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20190131 MGI PMID:28939830 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:16407890 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0005190 osteomyelitis IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0005571 decreased lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:22753929 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0005571 decreased lactate dehydrogenase level IAGP N RGD:5509061 20210318 MGI PMID:32342103 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:16546100 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20190131 MGI PMID:28939830 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008073 abnormal CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:21565393 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008608 increased circulating interleukin-13 level IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008623 increased circulating interleukin-3 level IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008627 decreased circulating interleukin-5 level IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008629 increased circulating interleukin-9 level IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:16546100 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:22002608 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:16546100 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:22002608 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008648 decreased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008656 abnormal interleukin-1 beta secretion IEA N RGD:5509061 20111116 MGI 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:16407889 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20457908 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20861349 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22002608 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22753929 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20181129 MGI PMID:28847925 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008684 increased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16407890 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16546100 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:22002608 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19501001 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20190131 MGI PMID:28939830 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16717117 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20190131 MGI PMID:28939830 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0011072 abnormal macrophage cytokine production IEA N RGD:5509061 20150122 MGI 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19501000 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20190131 MGI PMID:28939830 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20190131 MGI PMID:28939830 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0030825 decreased femur size IAGP N RGD:5509061 20181018 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0031110 meningitis IAGP N RGD:5509061 20200910 MGI PMID:22558291 1318015 Nlrp3 NLR family, pyrin domain containing 3 gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240321 MGI PMID:28939830 1318019 Abhd13 abhydrolase domain containing 13 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20200402 MGI 1318019 Abhd13 abhydrolase domain containing 13 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IEA N RGD:5509061 20230720 MGI 1318019 Abhd13 abhydrolase domain containing 13 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20201022 MGI 1318019 Abhd13 abhydrolase domain containing 13 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20210826 MGI 1318021 Mrps5 mitochondrial ribosomal protein S5 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1318021 Mrps5 mitochondrial ribosomal protein S5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318021 Mrps5 mitochondrial ribosomal protein S5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1318021 Mrps5 mitochondrial ribosomal protein S5 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1318022 Mtcl2 microtubule crosslinking factor 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20240523 MGI 1318022 Mtcl2 microtubule crosslinking factor 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20240523 MGI 1318026 Myf5 myogenic factor 5 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:11060232 1318026 Myf5 myogenic factor 5 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:18331721 1318026 Myf5 myogenic factor 5 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9268580 1318026 Myf5 myogenic factor 5 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:9268580 1318026 Myf5 myogenic factor 5 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:18331721 1318026 Myf5 myogenic factor 5 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9268580 1318026 Myf5 myogenic factor 5 gene MP:0000154 rib fusion IAGP N RGD:5509061 20160407 MGI PMID:25725491 1318026 Myf5 myogenic factor 5 gene MP:0000161 scoliosis IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21124733 1318026 Myf5 myogenic factor 5 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:11060232 1318026 Myf5 myogenic factor 5 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:11060232 1318026 Myf5 myogenic factor 5 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:15386014 1318026 Myf5 myogenic factor 5 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:21212806 1318026 Myf5 myogenic factor 5 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0000731 increased collagen deposition in the muscles IAGP N RGD:5509061 20141003 MGI PMID:23562821 1318026 Myf5 myogenic factor 5 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:14732408 1318026 Myf5 myogenic factor 5 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:15386014 1318026 Myf5 myogenic factor 5 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:17418413 1318026 Myf5 myogenic factor 5 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:19699733 1318026 Myf5 myogenic factor 5 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20231109 MGI PMID:36400788 1318026 Myf5 myogenic factor 5 gene MP:0000736 delayed muscle development IAGP N RGD:5509061 20141003 MGI PMID:17366633 1318026 Myf5 myogenic factor 5 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:10929709 1318026 Myf5 myogenic factor 5 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:11060232 1318026 Myf5 myogenic factor 5 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:1423602 1318026 Myf5 myogenic factor 5 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:9268580 1318026 Myf5 myogenic factor 5 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:17418413 1318026 Myf5 myogenic factor 5 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:17961534 1318026 Myf5 myogenic factor 5 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:23410975 1318026 Myf5 myogenic factor 5 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:22922256 1318026 Myf5 myogenic factor 5 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20220602 MGI PMID:35422047 1318026 Myf5 myogenic factor 5 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15386014 1318026 Myf5 myogenic factor 5 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17961534 1318026 Myf5 myogenic factor 5 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21956886 1318026 Myf5 myogenic factor 5 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20170831 MGI PMID:24938781 1318026 Myf5 myogenic factor 5 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20220602 MGI PMID:35422047 1318026 Myf5 myogenic factor 5 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19954518 1318026 Myf5 myogenic factor 5 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:19369542 1318026 Myf5 myogenic factor 5 gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19954518 1318026 Myf5 myogenic factor 5 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17158201 1318026 Myf5 myogenic factor 5 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23666760 1318026 Myf5 myogenic factor 5 gene MP:0001258 decreased body length IAGP N RGD:5509061 20180111 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17158201 1318026 Myf5 myogenic factor 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21124733 1318026 Myf5 myogenic factor 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22922256 1318026 Myf5 myogenic factor 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23562821 1318026 Myf5 myogenic factor 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180111 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220602 MGI PMID:35422047 1318026 Myf5 myogenic factor 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17418413 1318026 Myf5 myogenic factor 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21956886 1318026 Myf5 myogenic factor 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23410975 1318026 Myf5 myogenic factor 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23666760 1318026 Myf5 myogenic factor 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23933088 1318026 Myf5 myogenic factor 5 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19369542 1318026 Myf5 myogenic factor 5 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19369542 1318026 Myf5 myogenic factor 5 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:19369542 1318026 Myf5 myogenic factor 5 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17158201 1318026 Myf5 myogenic factor 5 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:1423602 1318026 Myf5 myogenic factor 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23562821 1318026 Myf5 myogenic factor 5 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141016 MGI PMID:24368734 1318026 Myf5 myogenic factor 5 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:21124733 1318026 Myf5 myogenic factor 5 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:11121437 1318026 Myf5 myogenic factor 5 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:1423602 1318026 Myf5 myogenic factor 5 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141016 MGI PMID:24368734 1318026 Myf5 myogenic factor 5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9268580 1318026 Myf5 myogenic factor 5 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17418413 1318026 Myf5 myogenic factor 5 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17418413 1318026 Myf5 myogenic factor 5 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20161110 MGI PMID:26844205 1318026 Myf5 myogenic factor 5 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15386014 1318026 Myf5 myogenic factor 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22922256 1318026 Myf5 myogenic factor 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23410975 1318026 Myf5 myogenic factor 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23562821 1318026 Myf5 myogenic factor 5 gene MP:0002083 premature death IAGP N RGD:5509061 20220602 MGI PMID:35422047 1318026 Myf5 myogenic factor 5 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:1423602 1318026 Myf5 myogenic factor 5 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141016 MGI PMID:24368734 1318026 Myf5 myogenic factor 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17418413 1318026 Myf5 myogenic factor 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23639729 1318026 Myf5 myogenic factor 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8587605 1318026 Myf5 myogenic factor 5 gene MP:0002253 abnormal pharyngeal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19531352 1318026 Myf5 myogenic factor 5 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19369542 1318026 Myf5 myogenic factor 5 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20161110 MGI PMID:26844205 1318026 Myf5 myogenic factor 5 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:11060232 1318026 Myf5 myogenic factor 5 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:11121437 1318026 Myf5 myogenic factor 5 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20161110 MGI PMID:26844205 1318026 Myf5 myogenic factor 5 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:19369542 1318026 Myf5 myogenic factor 5 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20180111 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11060232 1318026 Myf5 myogenic factor 5 gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17366633 1318026 Myf5 myogenic factor 5 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20201217 MGI PMID:31685980 1318026 Myf5 myogenic factor 5 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:15386014 1318026 Myf5 myogenic factor 5 gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:21956886 1318026 Myf5 myogenic factor 5 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:21124733 1318026 Myf5 myogenic factor 5 gene MP:0003154 abnormal soft palate morphology IAGP N RGD:5509061 20221027 MGI PMID:34557486 1318026 Myf5 myogenic factor 5 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20161110 MGI PMID:26844205 1318026 Myf5 myogenic factor 5 gene MP:0003794 delayed somite formation IAGP N RGD:5509061 20141003 MGI PMID:19531352 1318026 Myf5 myogenic factor 5 gene MP:0003818 abnormal eye muscle development IAGP N RGD:5509061 20141003 MGI PMID:19531352 1318026 Myf5 myogenic factor 5 gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:23562821 1318026 Myf5 myogenic factor 5 gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:23933088 1318026 Myf5 myogenic factor 5 gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:23562821 1318026 Myf5 myogenic factor 5 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17158201 1318026 Myf5 myogenic factor 5 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20180111 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:19369542 1318026 Myf5 myogenic factor 5 gene MP:0004094 abnormal M line morphology IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141016 MGI PMID:24368734 1318026 Myf5 myogenic factor 5 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:1423602 1318026 Myf5 myogenic factor 5 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:9268580 1318026 Myf5 myogenic factor 5 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:11060232 1318026 Myf5 myogenic factor 5 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:11060232 1318026 Myf5 myogenic factor 5 gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:11060232 1318026 Myf5 myogenic factor 5 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:11060232 1318026 Myf5 myogenic factor 5 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:1423602 1318026 Myf5 myogenic factor 5 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:7720708 1318026 Myf5 myogenic factor 5 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:8626014 1318026 Myf5 myogenic factor 5 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:9268580 1318026 Myf5 myogenic factor 5 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:17158201 1318026 Myf5 myogenic factor 5 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0004846 absent skeletal muscle IAGP N RGD:5509061 20141003 MGI PMID:15386014 1318026 Myf5 myogenic factor 5 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21124733 1318026 Myf5 myogenic factor 5 gene MP:0005150 cachexia IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0005247 abnormal extraocular muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19531352 1318026 Myf5 myogenic factor 5 gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20180111 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20161110 MGI PMID:26844205 1318026 Myf5 myogenic factor 5 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180111 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17158201 1318026 Myf5 myogenic factor 5 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21962509 1318026 Myf5 myogenic factor 5 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23666760 1318026 Myf5 myogenic factor 5 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21962509 1318026 Myf5 myogenic factor 5 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23666760 1318026 Myf5 myogenic factor 5 gene MP:0006320 abnormal interscapular fat pad morphology IAGP N RGD:5509061 20180111 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0006432 abnormal costal cartilage morphology IAGP N RGD:5509061 20160407 MGI PMID:25725491 1318026 Myf5 myogenic factor 5 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:18331721 1318026 Myf5 myogenic factor 5 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:1423602 1318026 Myf5 myogenic factor 5 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:7720708 1318026 Myf5 myogenic factor 5 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9268580 1318026 Myf5 myogenic factor 5 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:1423602 1318026 Myf5 myogenic factor 5 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:7720708 1318026 Myf5 myogenic factor 5 gene MP:0008486 decreased muscle spindle number IAGP N RGD:5509061 20141003 MGI PMID:19369542 1318026 Myf5 myogenic factor 5 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20220602 MGI PMID:35422047 1318026 Myf5 myogenic factor 5 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21212806 1318026 Myf5 myogenic factor 5 gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20180111 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20180111 MGI PMID:24196706 1318026 Myf5 myogenic factor 5 gene MP:0009137 decreased brown fat lipid droplet number IAGP N RGD:5509061 20180111 MGI PMID:24196706 1318026 Myf5 myogenic factor 5 gene MP:0009137 decreased brown fat lipid droplet number IAGP N RGD:5509061 20180111 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20180111 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20180111 MGI PMID:24196706 1318026 Myf5 myogenic factor 5 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:21124733 1318026 Myf5 myogenic factor 5 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:19699733 1318026 Myf5 myogenic factor 5 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20201217 MGI PMID:31685980 1318026 Myf5 myogenic factor 5 gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:17961534 1318026 Myf5 myogenic factor 5 gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:21124733 1318026 Myf5 myogenic factor 5 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:17366633 1318026 Myf5 myogenic factor 5 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:23933088 1318026 Myf5 myogenic factor 5 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:17961534 1318026 Myf5 myogenic factor 5 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:23562821 1318026 Myf5 myogenic factor 5 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20220602 MGI PMID:35422047 1318026 Myf5 myogenic factor 5 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:17961534 1318026 Myf5 myogenic factor 5 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:23562821 1318026 Myf5 myogenic factor 5 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20220602 MGI PMID:35422047 1318026 Myf5 myogenic factor 5 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:21124733 1318026 Myf5 myogenic factor 5 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:23933088 1318026 Myf5 myogenic factor 5 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0009410 abnormal skeletal muscle satellite cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17961534 1318026 Myf5 myogenic factor 5 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:17961534 1318026 Myf5 myogenic factor 5 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20220602 MGI PMID:35422047 1318026 Myf5 myogenic factor 5 gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:23562821 1318026 Myf5 myogenic factor 5 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17961534 1318026 Myf5 myogenic factor 5 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21124733 1318026 Myf5 myogenic factor 5 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23562821 1318026 Myf5 myogenic factor 5 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20220602 MGI PMID:35422047 1318026 Myf5 myogenic factor 5 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20201217 MGI PMID:31685980 1318026 Myf5 myogenic factor 5 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17158201 1318026 Myf5 myogenic factor 5 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:22922256 1318026 Myf5 myogenic factor 5 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20220602 MGI PMID:35422047 1318026 Myf5 myogenic factor 5 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:22922256 1318026 Myf5 myogenic factor 5 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:23562821 1318026 Myf5 myogenic factor 5 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20220602 MGI PMID:35422047 1318026 Myf5 myogenic factor 5 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:23562821 1318026 Myf5 myogenic factor 5 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20220602 MGI PMID:35422047 1318026 Myf5 myogenic factor 5 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20180111 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15386014 1318026 Myf5 myogenic factor 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17418413 1318026 Myf5 myogenic factor 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11060232 1318026 Myf5 myogenic factor 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11121437 1318026 Myf5 myogenic factor 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1423602 1318026 Myf5 myogenic factor 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18331721 1318026 Myf5 myogenic factor 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141016 MGI PMID:24368734 1318026 Myf5 myogenic factor 5 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20210401 MGI PMID:29168801 1318026 Myf5 myogenic factor 5 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8626014 1318026 Myf5 myogenic factor 5 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9268580 1318026 Myf5 myogenic factor 5 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9268580 1318026 Myf5 myogenic factor 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20221027 MGI PMID:34557486 1318026 Myf5 myogenic factor 5 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36400788 1318026 Myf5 myogenic factor 5 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36400788 1318026 Myf5 myogenic factor 5 gene MP:0011170 abnormal brown fat cell differentiation IAGP N RGD:5509061 20141016 MGI PMID:24368734 1318026 Myf5 myogenic factor 5 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20180111 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20180726 MGI PMID:29799007 1318026 Myf5 myogenic factor 5 gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20201217 MGI PMID:31685980 1318026 Myf5 myogenic factor 5 gene MP:0012185 abnormal muscle precursor cell morphology IAGP N RGD:5509061 20211125 MGI PMID:23562821 1318026 Myf5 myogenic factor 5 gene MP:0012186 abnormal muscle precursor cell physiology IAGP N RGD:5509061 20211125 MGI PMID:23562821 1318026 Myf5 myogenic factor 5 gene MP:0012249 absent myotome IAGP N RGD:5509061 20141003 MGI PMID:15386014 1318026 Myf5 myogenic factor 5 gene MP:0012249 absent myotome IAGP N RGD:5509061 20141003 MGI PMID:9268580 1318026 Myf5 myogenic factor 5 gene MP:0013237 abnormal skeletal muscle regeneration IAGP N RGD:5509061 20180726 MGI PMID:29799007 1318026 Myf5 myogenic factor 5 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:23933088 1318026 Myf5 myogenic factor 5 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:19699733 1318026 Myf5 myogenic factor 5 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:21124733 1318026 Myf5 myogenic factor 5 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:23562821 1318026 Myf5 myogenic factor 5 gene MP:0013546 cleft soft palate IAGP N RGD:5509061 20221027 MGI PMID:34557486 1318026 Myf5 myogenic factor 5 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20180111 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:21124733 1318026 Myf5 myogenic factor 5 gene MP:0014396 decreased fat cell mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:11060232 1318026 Myf5 myogenic factor 5 gene MP:0020520 whitened brown adipose tissue morphology IAGP N RGD:5509061 20180208 MGI PMID:24703692 1318026 Myf5 myogenic factor 5 gene MP:0021202 abnormal palatopharyngeus muscle morphology IAGP N RGD:5509061 20221103 MGI PMID:34557486 1318026 Myf5 myogenic factor 5 gene MP:0021204 abnormal superior pharyngeal constrictor muscle morphology IAGP N RGD:5509061 20221103 MGI PMID:34557486 1318026 Myf5 myogenic factor 5 gene MP:0030171 absent extraocular muscles IAGP N RGD:5509061 20171005 MGI PMID:19531352 1318026 Myf5 myogenic factor 5 gene MP:0030224 abnormal soft palate muscle morphology IAGP N RGD:5509061 20221027 MGI PMID:34557486 1318026 Myf5 myogenic factor 5 gene MP:0030292 abnormal tensor veli palatini muscle morphology IAGP N RGD:5509061 20221103 MGI PMID:34557486 1318026 Myf5 myogenic factor 5 gene MP:0030294 abnormal levator veli palatini muscle morphology IAGP N RGD:5509061 20221103 MGI PMID:34557486 1318026 Myf5 myogenic factor 5 gene MP:0030300 upper jaw to lower jaw transformation IAGP N RGD:5509061 20171102 MGI PMID:25725491 1318026 Myf5 myogenic factor 5 gene MP:0030957 abnormal myotube morphology IAGP N RGD:5509061 20190725 MGI PMID:11060232 1318026 Myf5 myogenic factor 5 gene MP:0031328 delayed skeletal muscle regeneration IAGP N RGD:5509061 20220106 MGI PMID:17366633 1318026 Myf5 myogenic factor 5 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:34557486 1318026 Myf5 myogenic factor 5 gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:26844205 1318028 Uba7 ubiquitin-like modifier activating enzyme 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16382139 1318028 Uba7 ubiquitin-like modifier activating enzyme 7 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:16382139 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20231102 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17889673 1318029 Uba6 ubiquitin-like modifier activating enzyme 6 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20141003 MGI PMID:23499007 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17220276 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:15919177 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:15919177 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15919177 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15919177 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15919177 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:15919177 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15919177 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15919177 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:15919177 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:17220276 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17220276 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15919177 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:17220276 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:17220276 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:17220276 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0004573 absent limb buds IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17220276 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0008409 increased cellular sensitivity to hydroxyurea IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:15919177 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15919177 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15919177 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0011705 absent fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:10921903 1318031 Hus1 HUS1 checkpoint clamp component gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:15919177 1318032 Dennd10 DENN domain containing 10 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1318032 Dennd10 DENN domain containing 10 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1318032 Dennd10 DENN domain containing 10 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1318032 Dennd10 DENN domain containing 10 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1318032 Dennd10 DENN domain containing 10 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 1318032 Dennd10 DENN domain containing 10 gene MP:0002764 short tibia IEA N RGD:5509061 20230119 MGI 1318037 Wwc1 WW, C2 and coiled-coil domain containing 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210603 MGI PMID:29116649 1318037 Wwc1 WW, C2 and coiled-coil domain containing 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20210603 MGI PMID:29116649 1318037 Wwc1 WW, C2 and coiled-coil domain containing 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21943600 1318037 Wwc1 WW, C2 and coiled-coil domain containing 1 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:21943600 1318037 Wwc1 WW, C2 and coiled-coil domain containing 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20210603 MGI PMID:29116649 1318037 Wwc1 WW, C2 and coiled-coil domain containing 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20210603 MGI PMID:29116649 1318037 Wwc1 WW, C2 and coiled-coil domain containing 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20210603 MGI PMID:29116649 1318037 Wwc1 WW, C2 and coiled-coil domain containing 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20210603 MGI PMID:29116649 1318037 Wwc1 WW, C2 and coiled-coil domain containing 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:24117625 1318037 Wwc1 WW, C2 and coiled-coil domain containing 1 gene MP:0008993 abnormal portal triad morphology IAGP N RGD:5509061 20210603 MGI PMID:29116649 1318037 Wwc1 WW, C2 and coiled-coil domain containing 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21943600 1318037 Wwc1 WW, C2 and coiled-coil domain containing 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21943600 1318037 Wwc1 WW, C2 and coiled-coil domain containing 1 gene MP:0012293 impaired active avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:24117625 1318037 Wwc1 WW, C2 and coiled-coil domain containing 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20141003 MGI PMID:24117625 1318041 Vps29 VPS29 retromer complex component gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20230119 MGI 1318041 Vps29 VPS29 retromer complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1318042 Eno4 enolase 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23446454 1318042 Eno4 enolase 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23446454 1318042 Eno4 enolase 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23446454 1318042 Eno4 enolase 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23446454 1318042 Eno4 enolase 4 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:23446454 1318042 Eno4 enolase 4 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:23446454 1318042 Eno4 enolase 4 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:23446454 1318042 Eno4 enolase 4 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:23446454 1318042 Eno4 enolase 4 gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20141003 MGI PMID:23446454 1318042 Eno4 enolase 4 gene MP:0009835 absent sperm annulus IAGP N RGD:5509061 20141003 MGI PMID:23446454 1318042 Eno4 enolase 4 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20141003 MGI PMID:23446454 1318042 Eno4 enolase 4 gene MP:0009837 abnormal sperm end piece morphology IAGP N RGD:5509061 20220217 MGI PMID:23446454 1318042 Eno4 enolase 4 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20141003 MGI PMID:23446454 1318042 Eno4 enolase 4 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20220217 MGI PMID:23446454 1318045 Ubxn10 UBX domain protein 10 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20201022 MGI 1318045 Ubxn10 UBX domain protein 10 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17668895 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22993422 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:18690222 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17668895 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:21493629 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:18690222 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:18690222 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18690222 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0008644 increased circulating interleukin-12a level IAGP N RGD:5509061 20141003 MGI PMID:18690222 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:18690222 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0008666 increased interleukin-12a secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:18690222 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18690222 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:18690222 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0009713 enhanced conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:16339038 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:16339038 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18690222 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:22993422 1318047 Rps6ka5 ribosomal protein S6 kinase, polypeptide 5 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:21493629 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20383150 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18241078 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:18241078 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:18241078 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18241078 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20383150 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20383150 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18241078 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18241078 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20383150 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:24204913 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18241078 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20141003 MGI PMID:18241078 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:20383150 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18241078 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:18241078 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0005462 abnormal mast cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24204913 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20383150 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20383150 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:24204913 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:20383150 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0009869 abnormal descending aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20383150 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318049 Patz1 POZ (BTB) and AT hook containing zinc finger 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22886576 1318051 Stk32a serine/threonine kinase 32A gene MP:0002623 abnormal vestibular hair cell morphology IAGP N RGD:5509061 20240822 MGI PMID:37144879 1318051 Stk32a serine/threonine kinase 32A gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20240822 MGI PMID:37144879 1318056 Ly9 lymphocyte antigen 9 gene MP:0002434 abnormal T-helper 2 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16365421 1318056 Ly9 lymphocyte antigen 9 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16365421 1318056 Ly9 lymphocyte antigen 9 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16365421 1318058 Cdh9 cadherin 9 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1318058 Cdh9 cadherin 9 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20180412 MGI PMID:25126785 1318058 Cdh9 cadherin 9 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:11960024 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:15269252 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141204 MGI PMID:25088982 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:22927954 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:11960024 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21052544 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:11960024 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:21052544 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:11960024 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:14507858 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15269252 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:19657028 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:22927954 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141204 MGI PMID:25088982 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:14507858 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19657028 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22927954 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:14507858 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22927954 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:11960024 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22927954 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22927954 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11960024 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21052544 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141204 MGI PMID:25088982 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141204 MGI PMID:25088982 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:14507858 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:22927954 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141204 MGI PMID:25088982 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0008581 disorganized photoreceptor inner segment IAGP N RGD:5509061 20141204 MGI PMID:25088982 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:21052544 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141204 MGI PMID:25088982 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141204 MGI PMID:25088982 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:21052544 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:22927954 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141204 MGI PMID:25088982 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20141204 MGI PMID:25088982 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20141204 MGI PMID:25088982 1318062 Rp1 retinitis pigmentosa 1 (human) gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:14507858 1318065 Tcl1 T cell lymphoma breakpoint 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12181493 1318065 Tcl1 T cell lymphoma breakpoint 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12181493 1318067 Trim37 tripartite motif-containing 37 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0001116 small gonad IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0001147 small testis IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0001263 weight loss IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0001924 infertility IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0001925 male infertility IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0001926 female infertility IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0002083 premature death IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0004806 absent germ cells IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0005324 ascites IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0005352 small cranium IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0008526 decreased cranium width IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20200310 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318067 Trim37 tripartite motif-containing 37 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20160915 MGI PMID:27044324 1318069 Inf2 inverted formin, FH2 and WH2 domain containing gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1318069 Inf2 inverted formin, FH2 and WH2 domain containing gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20180222 MGI PMID:29309034 1318069 Inf2 inverted formin, FH2 and WH2 domain containing gene MP:0002293 long gestation period IAGP N RGD:5509061 20180222 MGI PMID:29309034 1318069 Inf2 inverted formin, FH2 and WH2 domain containing gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20180222 MGI PMID:29309034 1318069 Inf2 inverted formin, FH2 and WH2 domain containing gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20180222 MGI PMID:29309034 1318069 Inf2 inverted formin, FH2 and WH2 domain containing gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20180222 MGI PMID:29309034 1318069 Inf2 inverted formin, FH2 and WH2 domain containing gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20180222 MGI PMID:29309034 1318069 Inf2 inverted formin, FH2 and WH2 domain containing gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20180222 MGI PMID:29309034 1318071 Cdc7 cell division cycle 7 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20201022 MGI 1318071 Cdc7 cell division cycle 7 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:14517263 1318071 Cdc7 cell division cycle 7 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:14517263 1318071 Cdc7 cell division cycle 7 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:14517263 1318071 Cdc7 cell division cycle 7 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:14517263 1318071 Cdc7 cell division cycle 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14517263 1318071 Cdc7 cell division cycle 7 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11980714 1318071 Cdc7 cell division cycle 7 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:14517263 1318071 Cdc7 cell division cycle 7 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1318071 Cdc7 cell division cycle 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14517263 1318071 Cdc7 cell division cycle 7 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:14517263 1318071 Cdc7 cell division cycle 7 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:14517263 1318071 Cdc7 cell division cycle 7 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:14517263 1318071 Cdc7 cell division cycle 7 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:14517263 1318071 Cdc7 cell division cycle 7 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:11980714 1318071 Cdc7 cell division cycle 7 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 1318071 Cdc7 cell division cycle 7 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:14517263 1318071 Cdc7 cell division cycle 7 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14517263 1318071 Cdc7 cell division cycle 7 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11980714 1318071 Cdc7 cell division cycle 7 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11980714 1318071 Cdc7 cell division cycle 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160811 MGI 1318071 Cdc7 cell division cycle 7 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14517263 1318071 Cdc7 cell division cycle 7 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1318071 Cdc7 cell division cycle 7 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1318071 Cdc7 cell division cycle 7 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:14517263 1318071 Cdc7 cell division cycle 7 gene MP:0021086 decreased DNA replication IAGP N RGD:5509061 20220310 MGI PMID:14517263 1318073 Ikbke inhibitor of kappaB kinase epsilon gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17332413 1318073 Ikbke inhibitor of kappaB kinase epsilon gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17332413 1318073 Ikbke inhibitor of kappaB kinase epsilon gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15210742 1318073 Ikbke inhibitor of kappaB kinase epsilon gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21371440 1318073 Ikbke inhibitor of kappaB kinase epsilon gene MP:0004892 increased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:21371440 1318073 Ikbke inhibitor of kappaB kinase epsilon gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21371440 1318073 Ikbke inhibitor of kappaB kinase epsilon gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21371440 1318073 Ikbke inhibitor of kappaB kinase epsilon gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:21371440 1318073 Ikbke inhibitor of kappaB kinase epsilon gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20230608 MGI PMID:17332413 1318073 Ikbke inhibitor of kappaB kinase epsilon gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:17332413 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20230824 MGI PMID:37359363 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230824 MGI PMID:37359363 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0003896 prolonged PR interval IEA N RGD:5509061 20211021 MGI 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20230824 MGI PMID:37359363 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20230824 MGI PMID:37359363 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20230824 MGI PMID:37359363 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20230824 MGI PMID:37359363 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20230824 MGI PMID:37359363 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20230824 MGI PMID:37359363 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0013615 increased volumetric bone mineral density IAGP N RGD:5509061 20230824 MGI PMID:37359363 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0013623 increased femur compact bone thickness IAGP N RGD:5509061 20230824 MGI PMID:37359363 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0013625 increased femur yield load IAGP N RGD:5509061 20230824 MGI PMID:37359363 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0013637 increased femur stiffness IAGP N RGD:5509061 20230824 MGI PMID:37359363 1318075 Rab33b RAB33B, member RAS oncogene family gene MP:0021191 increased bone mineral density of lumbar vertebrae IAGP N RGD:5509061 20230824 MGI PMID:37359363 1318078 C8a complement component 8, alpha polypeptide gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20201022 MGI 1318078 C8a complement component 8, alpha polypeptide gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1318078 C8a complement component 8, alpha polypeptide gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 1318083 Adamts19 ADAM metallopeptidase with thrombospondin type 1 motif 19 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20210506 MGI PMID:31844321 1318083 Adamts19 ADAM metallopeptidase with thrombospondin type 1 motif 19 gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20210506 MGI PMID:31844321 1318083 Adamts19 ADAM metallopeptidase with thrombospondin type 1 motif 19 gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20210506 MGI PMID:31844321 1318083 Adamts19 ADAM metallopeptidase with thrombospondin type 1 motif 19 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20210506 MGI PMID:31844321 1318083 Adamts19 ADAM metallopeptidase with thrombospondin type 1 motif 19 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20210506 MGI PMID:31844321 1318083 Adamts19 ADAM metallopeptidase with thrombospondin type 1 motif 19 gene MP:0010595 abnormal aortic valve cusp morphology IAGP N RGD:5509061 20210506 MGI PMID:31844321 1318083 Adamts19 ADAM metallopeptidase with thrombospondin type 1 motif 19 gene MP:0010598 abnormal aortic valve annulus morphology IAGP N RGD:5509061 20210506 MGI PMID:31844321 1318083 Adamts19 ADAM metallopeptidase with thrombospondin type 1 motif 19 gene MP:0011929 abnormal aortic valve flow IAGP N RGD:5509061 20210506 MGI PMID:31844321 1318083 Adamts19 ADAM metallopeptidase with thrombospondin type 1 motif 19 gene MP:0031166 abnormal aortic valve commissure morphology IAGP N RGD:5509061 20210506 MGI PMID:31844321 1318089 Txnrd3 thioredoxin reductase 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20221201 MGI PMID:35753352 1318089 Txnrd3 thioredoxin reductase 3 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20221201 MGI PMID:35753352 1318089 Txnrd3 thioredoxin reductase 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20221201 MGI PMID:35753352 1318089 Txnrd3 thioredoxin reductase 3 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20221201 MGI PMID:35753352 1318090 Pcdhb10 protocadherin beta 10 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220519 MGI 1318090 Pcdhb10 protocadherin beta 10 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220519 MGI 1318090 Pcdhb10 protocadherin beta 10 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0000161 scoliosis IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318092 Ssr2 signal sequence receptor, beta gene MP:0000825 dilated lateral ventricle IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0001330 abnormal optic nerve morphology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0001916 intracerebral hemorrhage IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0002279 abnormal diaphragm morphology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0004057 thin myocardium compact layer IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0004201 fetal growth retardation IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0004463 basisphenoid bone foramen IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0005244 hemopericardium IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0008536 enlarged third ventricle IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318092 Ssr2 signal sequence receptor, beta gene MP:0009770 abnormal optic chiasm morphology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0009913 abnormal hyoid bone greater horn morphology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318092 Ssr2 signal sequence receptor, beta gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0010490 abnormal inferior vena cava valve morphology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0010589 common truncal valve IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0010592 abnormal atrioventricular septum morphology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0010602 abnormal pulmonary valve cusp morphology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318092 Ssr2 signal sequence receptor, beta gene MP:0011659 interrupted aortic arch, type b IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0013815 abnormal digastric muscle morphology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0013875 increased trigeminal neuroma incidence IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0013973 abnormal hepatic vein connection IEA N RGD:5509061 20170504 MGI 1318092 Ssr2 signal sequence receptor, beta gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1318094 Rhpn2 rhophilin, Rho GTPase binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20191003 MGI PMID:25071083 1318094 Rhpn2 rhophilin, Rho GTPase binding protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15767687 1318094 Rhpn2 rhophilin, Rho GTPase binding protein 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20191003 MGI PMID:25071083 1318094 Rhpn2 rhophilin, Rho GTPase binding protein 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20191003 MGI PMID:25071083 1318094 Rhpn2 rhophilin, Rho GTPase binding protein 2 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20191003 MGI PMID:25071083 1318094 Rhpn2 rhophilin, Rho GTPase binding protein 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20191003 MGI PMID:25071083 1318094 Rhpn2 rhophilin, Rho GTPase binding protein 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20191003 MGI PMID:25071083 1318094 Rhpn2 rhophilin, Rho GTPase binding protein 2 gene MP:0011402 renal cast IAGP N RGD:5509061 20191003 MGI PMID:25071083 1318096 Ermn ermin, ERM-like protein gene MP:0000921 demyelination IAGP N RGD:5509061 20220210 MGI PMID:32530539 1318096 Ermn ermin, ERM-like protein gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20220210 MGI PMID:32530539 1318096 Ermn ermin, ERM-like protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20220210 MGI PMID:32530539 1318096 Ermn ermin, ERM-like protein gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1318096 Ermn ermin, ERM-like protein gene MP:0005505 thrombocytosis IEA N RGD:5509061 20240523 MGI 1318096 Ermn ermin, ERM-like protein gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20190502 MGI 1318096 Ermn ermin, ERM-like protein gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20220210 MGI PMID:32530539 1318098 Mgam maltase-glucoamylase gene MP:0002715 decreased glycogen catabolism rate IAGP N RGD:5509061 20141003 MGI PMID:19193815 1318098 Mgam maltase-glucoamylase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19193815 1318098 Mgam maltase-glucoamylase gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:17585022 1318098 Mgam maltase-glucoamylase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17585022 1318098 Mgam maltase-glucoamylase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:19193815 1318100 Samhd1 SAM domain and HD domain, 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23972988 1318100 Samhd1 SAM domain and HD domain, 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:23972988 1318100 Samhd1 SAM domain and HD domain, 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23972988 1318100 Samhd1 SAM domain and HD domain, 1 gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:23872947 1318102 Tmem126b transmembrane protein 126B gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20201224 MGI PMID:30580996 1318102 Tmem126b transmembrane protein 126B gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20201224 MGI PMID:30580996 1318107 Sirt3 sirtuin 3 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0001406 abnormal gait IEA N RGD:5509061 20170105 MGI 1318107 Sirt3 sirtuin 3 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17923681 1318107 Sirt3 sirtuin 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20220630 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1318107 Sirt3 sirtuin 3 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20201231 MGI 1318107 Sirt3 sirtuin 3 gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20200123 MGI PMID:27681422 1318107 Sirt3 sirtuin 3 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18794531 1318107 Sirt3 sirtuin 3 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0006144 increased systemic arterial systolic blood pressure IEA N RGD:5509061 20111116 MGI 1318107 Sirt3 sirtuin 3 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21856199 1318107 Sirt3 sirtuin 3 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 1318107 Sirt3 sirtuin 3 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:18794531 1318107 Sirt3 sirtuin 3 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21856199 1318109 Plaat5 phospholipase A and acyltransferase 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1318109 Plaat5 phospholipase A and acyltransferase 5 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1318109 Plaat5 phospholipase A and acyltransferase 5 gene MP:0009453 enhanced contextual conditioning behavior IEA N RGD:5509061 20210128 MGI 1318113 Ctrc chymotrypsin C gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20201231 MGI 1318113 Ctrc chymotrypsin C gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20210128 MGI 1318113 Ctrc chymotrypsin C gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20200820 MGI PMID:31211695 1318113 Ctrc chymotrypsin C gene MP:0009476 enlarged cecum IEA N RGD:5509061 20200514 MGI 1318114 Trmt44 tRNA methyltransferase 44 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1318116 Map3k10 mitogen-activated protein kinase kinase kinase 10 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160421 MGI 1318116 Map3k10 mitogen-activated protein kinase kinase kinase 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18414056 1318116 Map3k10 mitogen-activated protein kinase kinase kinase 10 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:21979919 1318116 Map3k10 mitogen-activated protein kinase kinase kinase 10 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1318116 Map3k10 mitogen-activated protein kinase kinase kinase 10 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:21979919 1318116 Map3k10 mitogen-activated protein kinase kinase kinase 10 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:21979919 1318118 Cdc42ep5 CDC42 effector protein 5 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20181227 MGI 1318118 Cdc42ep5 CDC42 effector protein 5 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1318118 Cdc42ep5 CDC42 effector protein 5 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1318118 Cdc42ep5 CDC42 effector protein 5 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1318127 Mttp microsomal triglyceride transfer protein gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10037685 1318127 Mttp microsomal triglyceride transfer protein gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10037685 1318127 Mttp microsomal triglyceride transfer protein gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12588952 1318127 Mttp microsomal triglyceride transfer protein gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10037685 1318127 Mttp microsomal triglyceride transfer protein gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12588952 1318127 Mttp microsomal triglyceride transfer protein gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10037685 1318127 Mttp microsomal triglyceride transfer protein gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:12588952 1318127 Mttp microsomal triglyceride transfer protein gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12588952 1318127 Mttp microsomal triglyceride transfer protein gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:12588952 1318127 Mttp microsomal triglyceride transfer protein gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10037685 1318127 Mttp microsomal triglyceride transfer protein gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10037685 1318127 Mttp microsomal triglyceride transfer protein gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12588952 1318127 Mttp microsomal triglyceride transfer protein gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12588952 1318127 Mttp microsomal triglyceride transfer protein gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:12588952 1318127 Mttp microsomal triglyceride transfer protein gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12588952 1318127 Mttp microsomal triglyceride transfer protein gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12588952 1318127 Mttp microsomal triglyceride transfer protein gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20180125 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:9671739 1318127 Mttp microsomal triglyceride transfer protein gene MP:0020515 abnormal visceral yolk sac endoderm morphology IAGP N RGD:5509061 20180125 MGI PMID:9671739 1318129 Zdhhc4 zinc finger, DHHC domain containing 4 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20191024 MGI PMID:30605677 1318129 Zdhhc4 zinc finger, DHHC domain containing 4 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20191024 MGI PMID:30605677 1318129 Zdhhc4 zinc finger, DHHC domain containing 4 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20191024 MGI PMID:30605677 1318129 Zdhhc4 zinc finger, DHHC domain containing 4 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20191024 MGI PMID:30605677 1318129 Zdhhc4 zinc finger, DHHC domain containing 4 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20191024 MGI PMID:30605677 1318131 Serinc3 serine incorporator 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210520 MGI 1318131 Serinc3 serine incorporator 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:32665269 1318131 Serinc3 serine incorporator 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1318131 Serinc3 serine incorporator 3 gene MP:0010093 decreased circulating magnesium level IEA N RGD:5509061 20150430 MGI 1318131 Serinc3 serine incorporator 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1318133 Mzf1 myeloid zinc finger 1 gene MP:0000168 abnormal bone marrow development IAGP N RGD:5509061 20141003 MGI PMID:11445537 1318133 Mzf1 myeloid zinc finger 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11445537 1318133 Mzf1 myeloid zinc finger 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11445537 1318133 Mzf1 myeloid zinc finger 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11445537 1318133 Mzf1 myeloid zinc finger 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11445537 1318133 Mzf1 myeloid zinc finger 1 gene MP:0005649 increased spleen neoplasm incidence IAGP N RGD:5509061 20141003 MGI PMID:11445537 1318135 Hibch 3-hydroxyisobutyryl-Coenzyme A hydrolase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1318135 Hibch 3-hydroxyisobutyryl-Coenzyme A hydrolase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1318135 Hibch 3-hydroxyisobutyryl-Coenzyme A hydrolase gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20201022 MGI 1318135 Hibch 3-hydroxyisobutyryl-Coenzyme A hydrolase gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20201022 MGI 1318135 Hibch 3-hydroxyisobutyryl-Coenzyme A hydrolase gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20201022 MGI 1318135 Hibch 3-hydroxyisobutyryl-Coenzyme A hydrolase gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20201022 MGI 1318135 Hibch 3-hydroxyisobutyryl-Coenzyme A hydrolase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1318135 Hibch 3-hydroxyisobutyryl-Coenzyme A hydrolase gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20201022 MGI 1318135 Hibch 3-hydroxyisobutyryl-Coenzyme A hydrolase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200514 MGI 1318135 Hibch 3-hydroxyisobutyryl-Coenzyme A hydrolase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1318144 Odf2l outer dense fiber of sperm tails 2-like gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1318144 Odf2l outer dense fiber of sperm tails 2-like gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1318144 Odf2l outer dense fiber of sperm tails 2-like gene MP:0009084 blind uterus IEA N RGD:5509061 20201022 MGI 1318145 Lrrc26 leucine rich repeat containing 26 gene MP:0005310 abnormal salivary gland physiology IAGP N RGD:5509061 20180111 MGI PMID:28416688 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0000111 cleft palate IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0004343 small scapula IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0005109 abnormal talus morphology IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0010484 bicuspid aortic valve IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0010530 cerebral arteriovenous malformation IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0011493 double ureter IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0012303 umbilical vein stenosis IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0013842 ductus venosus stenosis IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0013843 hepatic portal vein stenosis IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0013844 abnormal perichondrial ossification IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0013845 abnormal eye muscle topology IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0014003 additional anastomosis between intracranial vertebral arteries IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0014019 embryo cyst IEA N RGD:5509061 20170504 MGI 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0030384 short facial bone IAGP N RGD:5509061 20171207 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0030848 short ilium IAGP N RGD:5509061 20181025 MGI PMID:16079159 1318148 Chst11 carbohydrate sulfotransferase 11 gene MP:0030849 wide ilium IAGP N RGD:5509061 20181025 MGI PMID:16079159 1318159 Hapln4 hyaluronan and proteoglycan link protein 4 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20180830 MGI PMID:22121037 1318159 Hapln4 hyaluronan and proteoglycan link protein 4 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20180830 MGI PMID:22121037 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20240229 MGI PMID:29961073 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17329413 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:15207856 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:15606908 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:15820310 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15820310 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0001967 deafness IAGP N RGD:5509061 20160929 MGI PMID:27534441 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0001967 deafness IAGP N RGD:5509061 20240229 MGI PMID:29961073 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:15820310 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0003146 absent cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:17295842 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0003637 cochlear ganglion hypoplasia IAGP N RGD:5509061 20240229 MGI PMID:29961073 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15820310 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17295842 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20141003 MGI PMID:17567809 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17567809 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:17329413 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:17567809 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15820310 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:17295842 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:17567809 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20240229 MGI PMID:29961073 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:17567809 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004577 abnormal cochlear hair cell inter-stereocilial links morphology IAGP N RGD:5509061 20141003 MGI PMID:17295842 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004582 absent cochlear hair bundle ankle links IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004582 absent cochlear hair bundle ankle links IAGP N RGD:5509061 20141003 MGI PMID:17567809 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004586 pillar cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:17295842 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:15820310 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15207856 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15606908 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15820310 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16775142 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17295842 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17329413 1318162 Adgrv1 adhesion G protein-coupled receptor V1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20240229 MGI PMID:29961073 1318166 Krtcap2 keratinocyte associated protein 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 1318166 Krtcap2 keratinocyte associated protein 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220811 MGI 1318166 Krtcap2 keratinocyte associated protein 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220811 MGI 1318166 Krtcap2 keratinocyte associated protein 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1318166 Krtcap2 keratinocyte associated protein 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220811 MGI 1318166 Krtcap2 keratinocyte associated protein 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220811 MGI 1318166 Krtcap2 keratinocyte associated protein 2 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20231207 MGI 1318166 Krtcap2 keratinocyte associated protein 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220811 MGI 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0002064 seizures IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318169 Sh3rf2 SH3 domain containing ring finger 2 gene MP:0020507 increased dendritic spine density IAGP N RGD:5509061 20200611 MGI PMID:30540932 1318171 Jph3 junctophilin 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16809425 1318171 Jph3 junctophilin 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16809425 1318171 Jph3 junctophilin 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11906164 1318171 Jph3 junctophilin 3 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:16809425 1318171 Jph3 junctophilin 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16809425 1318171 Jph3 junctophilin 3 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16809425 1318171 Jph3 junctophilin 3 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:16809425 1318171 Jph3 junctophilin 3 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:16809425 1318171 Jph3 junctophilin 3 gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:16809425 1318171 Jph3 junctophilin 3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:16809425 1318171 Jph3 junctophilin 3 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20141003 MGI PMID:16809425 1318171 Jph3 junctophilin 3 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:16809425 1318171 Jph3 junctophilin 3 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16809425 1318171 Jph3 junctophilin 3 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:16809425 1318173 Hoxd13 homeobox D13 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:8106170 1318173 Hoxd13 homeobox D13 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:8787740 1318173 Hoxd13 homeobox D13 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:8978698 1318173 Hoxd13 homeobox D13 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:8674109 1318173 Hoxd13 homeobox D13 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8106170 1318173 Hoxd13 homeobox D13 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8620844 1318173 Hoxd13 homeobox D13 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8674109 1318173 Hoxd13 homeobox D13 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8978698 1318173 Hoxd13 homeobox D13 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9580668 1318173 Hoxd13 homeobox D13 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9659925 1318173 Hoxd13 homeobox D13 gene MP:0000555 absent carpal bone IAGP N RGD:5509061 20141003 MGI PMID:8620844 1318173 Hoxd13 homeobox D13 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:11543619 1318173 Hoxd13 homeobox D13 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:8106170 1318173 Hoxd13 homeobox D13 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:8620844 1318173 Hoxd13 homeobox D13 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:8978698 1318173 Hoxd13 homeobox D13 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9580668 1318173 Hoxd13 homeobox D13 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9659925 1318173 Hoxd13 homeobox D13 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:11543619 1318173 Hoxd13 homeobox D13 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:8106170 1318173 Hoxd13 homeobox D13 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:9580668 1318173 Hoxd13 homeobox D13 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:8620844 1318173 Hoxd13 homeobox D13 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:11543619 1318173 Hoxd13 homeobox D13 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0000767 abnormal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8787740 1318173 Hoxd13 homeobox D13 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8106170 1318173 Hoxd13 homeobox D13 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8978698 1318173 Hoxd13 homeobox D13 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11543619 1318173 Hoxd13 homeobox D13 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:9659925 1318173 Hoxd13 homeobox D13 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8106170 1318173 Hoxd13 homeobox D13 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8978698 1318173 Hoxd13 homeobox D13 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9580668 1318173 Hoxd13 homeobox D13 gene MP:0002059 abnormal seminal vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9580668 1318173 Hoxd13 homeobox D13 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8978698 1318173 Hoxd13 homeobox D13 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8106170 1318173 Hoxd13 homeobox D13 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:8106170 1318173 Hoxd13 homeobox D13 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:8620844 1318173 Hoxd13 homeobox D13 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:8787740 1318173 Hoxd13 homeobox D13 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:8978698 1318173 Hoxd13 homeobox D13 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9580668 1318173 Hoxd13 homeobox D13 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9659925 1318173 Hoxd13 homeobox D13 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:11543619 1318173 Hoxd13 homeobox D13 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:8106170 1318173 Hoxd13 homeobox D13 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:8620844 1318173 Hoxd13 homeobox D13 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:8674109 1318173 Hoxd13 homeobox D13 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:8787740 1318173 Hoxd13 homeobox D13 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:8978698 1318173 Hoxd13 homeobox D13 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:8106170 1318173 Hoxd13 homeobox D13 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:8674109 1318173 Hoxd13 homeobox D13 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:8787740 1318173 Hoxd13 homeobox D13 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:9580668 1318173 Hoxd13 homeobox D13 gene MP:0002772 brachypodia IAGP N RGD:5509061 20141003 MGI PMID:11543619 1318173 Hoxd13 homeobox D13 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11543619 1318173 Hoxd13 homeobox D13 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8106170 1318173 Hoxd13 homeobox D13 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9659925 1318173 Hoxd13 homeobox D13 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8978698 1318173 Hoxd13 homeobox D13 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11543619 1318173 Hoxd13 homeobox D13 gene MP:0003800 monodactyly IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:8674109 1318173 Hoxd13 homeobox D13 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:8674109 1318173 Hoxd13 homeobox D13 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20141003 MGI PMID:8674109 1318173 Hoxd13 homeobox D13 gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:8674109 1318173 Hoxd13 homeobox D13 gene MP:0004576 abnormal embryonic autopod plate morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0004622 sacral vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:8106170 1318173 Hoxd13 homeobox D13 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:8106170 1318173 Hoxd13 homeobox D13 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:8620844 1318173 Hoxd13 homeobox D13 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:9580668 1318173 Hoxd13 homeobox D13 gene MP:0004635 short metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:8106170 1318173 Hoxd13 homeobox D13 gene MP:0004635 short metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:9580668 1318173 Hoxd13 homeobox D13 gene MP:0004636 decreased metacarpal bone number IAGP N RGD:5509061 20141003 MGI PMID:9580668 1318173 Hoxd13 homeobox D13 gene MP:0004640 decreased metatarsal bone number IAGP N RGD:5509061 20141003 MGI PMID:9580668 1318173 Hoxd13 homeobox D13 gene MP:0004641 elongated metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0005034 abnormal anus morphology IAGP N RGD:5509061 20141003 MGI PMID:8787740 1318173 Hoxd13 homeobox D13 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8978698 1318173 Hoxd13 homeobox D13 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9580668 1318173 Hoxd13 homeobox D13 gene MP:0005230 ectrodactyly IAGP N RGD:5509061 20141003 MGI PMID:11543619 1318173 Hoxd13 homeobox D13 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:11543619 1318173 Hoxd13 homeobox D13 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:8106170 1318173 Hoxd13 homeobox D13 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:8978698 1318173 Hoxd13 homeobox D13 gene MP:0006230 iris stroma hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11543619 1318173 Hoxd13 homeobox D13 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:11543619 1318173 Hoxd13 homeobox D13 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0006401 absent male preputial gland IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0006401 absent male preputial gland IAGP N RGD:5509061 20141003 MGI PMID:9580668 1318173 Hoxd13 homeobox D13 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9580668 1318173 Hoxd13 homeobox D13 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:11543619 1318173 Hoxd13 homeobox D13 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0008919 fused tarsal bones IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0009049 abnormal hallux morphology IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0009055 abnormal internal anal sphincter morphology IAGP N RGD:5509061 20141003 MGI PMID:8787740 1318173 Hoxd13 homeobox D13 gene MP:0009380 abnormal prostate gland ventral lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:12668621 1318173 Hoxd13 homeobox D13 gene MP:0009744 postaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19546318 1318173 Hoxd13 homeobox D13 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8898214 1318173 Hoxd13 homeobox D13 gene MP:0013901 absent female preputial gland IAGP N RGD:5509061 20150924 MGI PMID:9580668 1318173 Hoxd13 homeobox D13 gene MP:0014291 decreased autopod size IAGP N RGD:5509061 20230824 MGI PMID:8898214 1318176 Rora RAR-related orphan receptor alpha gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9851961 1318176 Rora RAR-related orphan receptor alpha gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:11964376 1318176 Rora RAR-related orphan receptor alpha gene MP:0000408 absent duvet hair IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0000424 retarded hair growth IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9510031 1318176 Rora RAR-related orphan receptor alpha gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:10321020 1318176 Rora RAR-related orphan receptor alpha gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:1511513 1318176 Rora RAR-related orphan receptor alpha gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:368650 1318176 Rora RAR-related orphan receptor alpha gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:6960362 1318176 Rora RAR-related orphan receptor alpha gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:723931 1318176 Rora RAR-related orphan receptor alpha gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:1511513 1318176 Rora RAR-related orphan receptor alpha gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:4673255 1318176 Rora RAR-related orphan receptor alpha gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:6127146 1318176 Rora RAR-related orphan receptor alpha gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9510031 1318176 Rora RAR-related orphan receptor alpha gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:641237 1318176 Rora RAR-related orphan receptor alpha gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:2077109 1318176 Rora RAR-related orphan receptor alpha gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:466453 1318176 Rora RAR-related orphan receptor alpha gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7352029 1318176 Rora RAR-related orphan receptor alpha gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:1511513 1318176 Rora RAR-related orphan receptor alpha gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:9510031 1318176 Rora RAR-related orphan receptor alpha gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0000884 delaminated Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:641237 1318176 Rora RAR-related orphan receptor alpha gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:9510031 1318176 Rora RAR-related orphan receptor alpha gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:1511513 1318176 Rora RAR-related orphan receptor alpha gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:641237 1318176 Rora RAR-related orphan receptor alpha gene MP:0000888 absent cerebellar granule layer IEA N RGD:5509061 20111116 MGI 1318176 Rora RAR-related orphan receptor alpha gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:641237 1318176 Rora RAR-related orphan receptor alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:8346298 1318176 Rora RAR-related orphan receptor alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:8013566 1318176 Rora RAR-related orphan receptor alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:8577876 1318176 Rora RAR-related orphan receptor alpha gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:8848495 1318176 Rora RAR-related orphan receptor alpha gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0001523 impaired righting response IEA N RGD:5509061 20111116 MGI 1318176 Rora RAR-related orphan receptor alpha gene MP:0001524 impaired limb coordination IEA N RGD:5509061 20111116 MGI 1318176 Rora RAR-related orphan receptor alpha gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:9510031 1318176 Rora RAR-related orphan receptor alpha gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:11964376 1318176 Rora RAR-related orphan receptor alpha gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:1565842 1318176 Rora RAR-related orphan receptor alpha gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:16973978 1318176 Rora RAR-related orphan receptor alpha gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:1590727 1318176 Rora RAR-related orphan receptor alpha gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:1590727 1318176 Rora RAR-related orphan receptor alpha gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:10696797 1318176 Rora RAR-related orphan receptor alpha gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:9035249 1318176 Rora RAR-related orphan receptor alpha gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9851961 1318176 Rora RAR-related orphan receptor alpha gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:8352721 1318176 Rora RAR-related orphan receptor alpha gene MP:0002277 abnormal respiratory mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:16973978 1318176 Rora RAR-related orphan receptor alpha gene MP:0002333 abnormal lung compliance IAGP N RGD:5509061 20141003 MGI PMID:16973978 1318176 Rora RAR-related orphan receptor alpha gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:2230805 1318176 Rora RAR-related orphan receptor alpha gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16973978 1318176 Rora RAR-related orphan receptor alpha gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20160915 MGI PMID:7667406 1318176 Rora RAR-related orphan receptor alpha gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20160915 MGI PMID:8352721 1318176 Rora RAR-related orphan receptor alpha gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:1565842 1318176 Rora RAR-related orphan receptor alpha gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:10321020 1318176 Rora RAR-related orphan receptor alpha gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 1318176 Rora RAR-related orphan receptor alpha gene MP:0003126 abnormal external female genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:1590727 1318176 Rora RAR-related orphan receptor alpha gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:2901364 1318176 Rora RAR-related orphan receptor alpha gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:1565842 1318176 Rora RAR-related orphan receptor alpha gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:1565842 1318176 Rora RAR-related orphan receptor alpha gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0003684 abnormal inferior olivary complex morphology IAGP N RGD:5509061 20141003 MGI PMID:1511513 1318176 Rora RAR-related orphan receptor alpha gene MP:0003684 abnormal inferior olivary complex morphology IAGP N RGD:5509061 20141003 MGI PMID:2231177 1318176 Rora RAR-related orphan receptor alpha gene MP:0003684 abnormal inferior olivary complex morphology IAGP N RGD:5509061 20141003 MGI PMID:7842506 1318176 Rora RAR-related orphan receptor alpha gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:1590727 1318176 Rora RAR-related orphan receptor alpha gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:2123001 1318176 Rora RAR-related orphan receptor alpha gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:4673255 1318176 Rora RAR-related orphan receptor alpha gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:641237 1318176 Rora RAR-related orphan receptor alpha gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0004494 abnormal synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:6127146 1318176 Rora RAR-related orphan receptor alpha gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11964376 1318176 Rora RAR-related orphan receptor alpha gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9851961 1318176 Rora RAR-related orphan receptor alpha gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:9851961 1318176 Rora RAR-related orphan receptor alpha gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9851961 1318176 Rora RAR-related orphan receptor alpha gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11739287 1318176 Rora RAR-related orphan receptor alpha gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:641237 1318176 Rora RAR-related orphan receptor alpha gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:641237 1318176 Rora RAR-related orphan receptor alpha gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0008579 abnormal Purkinje cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:641237 1318176 Rora RAR-related orphan receptor alpha gene MP:0008651 increased interleukin-1 secretion IAGP N RGD:5509061 20141003 MGI PMID:2230805 1318176 Rora RAR-related orphan receptor alpha gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:1511513 1318176 Rora RAR-related orphan receptor alpha gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:4673255 1318176 Rora RAR-related orphan receptor alpha gene MP:0009008 delayed estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:1590727 1318176 Rora RAR-related orphan receptor alpha gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20141003 MGI PMID:1590727 1318176 Rora RAR-related orphan receptor alpha gene MP:0009020 prolonged metestrus IAGP N RGD:5509061 20141003 MGI PMID:1590727 1318176 Rora RAR-related orphan receptor alpha gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0009942 abnormal olfactory bulb granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10321020 1318176 Rora RAR-related orphan receptor alpha gene MP:0009946 abnormal olfactory bulb layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10321020 1318176 Rora RAR-related orphan receptor alpha gene MP:0009947 abnormal olfactory bulb external plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10321020 1318176 Rora RAR-related orphan receptor alpha gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10321020 1318176 Rora RAR-related orphan receptor alpha gene MP:0009949 abnormal olfactory bulb granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10321020 1318176 Rora RAR-related orphan receptor alpha gene MP:0009950 abnormal olfactory bulb internal plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10321020 1318176 Rora RAR-related orphan receptor alpha gene MP:0009951 abnormal olfactory bulb mitral cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10321020 1318176 Rora RAR-related orphan receptor alpha gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20141003 MGI PMID:1511513 1318176 Rora RAR-related orphan receptor alpha gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20141003 MGI PMID:4673255 1318176 Rora RAR-related orphan receptor alpha gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20141003 MGI PMID:641237 1318176 Rora RAR-related orphan receptor alpha gene MP:0009958 absent cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0009979 abnormal cerebellum deep nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:7260600 1318176 Rora RAR-related orphan receptor alpha gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0010057 abnormal olfactory bulb outer nerve layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10321020 1318176 Rora RAR-related orphan receptor alpha gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9520475 1318176 Rora RAR-related orphan receptor alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9510031 1318176 Rora RAR-related orphan receptor alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:13912552 1318176 Rora RAR-related orphan receptor alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1318176 Rora RAR-related orphan receptor alpha gene MP:0012490 abnormal cochlear VIII nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:2077109 1318176 Rora RAR-related orphan receptor alpha gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20180913 MGI PMID:6123371 1318176 Rora RAR-related orphan receptor alpha gene MP:0013551 decreased cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20161201 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:20722722 1318176 Rora RAR-related orphan receptor alpha gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:641237 1318176 Rora RAR-related orphan receptor alpha gene MP:0030636 decreased taurine level IAGP N RGD:5509061 20180913 MGI PMID:6127146 1318176 Rora RAR-related orphan receptor alpha gene MP:0030733 decreased gamma-aminobutyric acid level IAGP N RGD:5509061 20180927 MGI PMID:6127146 1318176 Rora RAR-related orphan receptor alpha gene MP:0030743 decreased aspartic acid level IAGP N RGD:5509061 20180927 MGI PMID:6127146 1318178 Mcoln3 mucolipin 3 gene MP:0000048 abnormal stria vascularis morphology IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:12209292 1318178 Mcoln3 mucolipin 3 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:4557539 1318178 Mcoln3 mucolipin 3 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:12209292 1318178 Mcoln3 mucolipin 3 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:4557539 1318178 Mcoln3 mucolipin 3 gene MP:0000421 mottled coat IAGP N RGD:5509061 20141003 MGI PMID:12209292 1318178 Mcoln3 mucolipin 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:4557539 1318178 Mcoln3 mucolipin 3 gene MP:0001386 abnormal maternal nurturing IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:4557539 1318178 Mcoln3 mucolipin 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0001401 jumpy IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0001405 impaired coordination IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0001408 stereotypic behavior IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:4557539 1318178 Mcoln3 mucolipin 3 gene MP:0001523 impaired righting response IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:4557539 1318178 Mcoln3 mucolipin 3 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:12209292 1318178 Mcoln3 mucolipin 3 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:4557539 1318178 Mcoln3 mucolipin 3 gene MP:0002622 abnormal cochlear hair cell morphology IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0002826 tonic seizures IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0002856 abnormal vestibular ganglion morphology IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0002857 cochlear ganglion degeneration IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:12209292 1318178 Mcoln3 mucolipin 3 gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:4557539 1318178 Mcoln3 mucolipin 3 gene MP:0002939 head spot IAGP N RGD:5509061 20141003 MGI PMID:12209292 1318178 Mcoln3 mucolipin 3 gene MP:0003150 detached tectorial membrane IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0003312 abnormal locomotor coordination IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0004249 abnormal crista ampullaris morphology IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0004362 cochlear hair cell degeneration IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0004591 enlarged tectorial membrane IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0005175 non-pigmented tail tip IAGP N RGD:5509061 20141003 MGI PMID:4557539 1318178 Mcoln3 mucolipin 3 gene MP:0005307 head tossing IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0005366 variegated coat color IEA N RGD:5509061 20111116 MGI 1318178 Mcoln3 mucolipin 3 gene MP:0009379 abnormal foot pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4557539 1318178 Mcoln3 mucolipin 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12209292 1318178 Mcoln3 mucolipin 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:4557539 1318178 Mcoln3 mucolipin 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12209292 1318180 Muc16 mucin 16 gene MP:0001934 increased litter size IAGP N RGD:5509061 20141003 MGI PMID:19262696 1318182 Taf8 TATA-box binding protein associated factor 8 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20210422 MGI 1318182 Taf8 TATA-box binding protein associated factor 8 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:11076765 1318182 Taf8 TATA-box binding protein associated factor 8 gene MP:0009709 hydrometra IEA N RGD:5509061 20210422 MGI 1318182 Taf8 TATA-box binding protein associated factor 8 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11076765 1318182 Taf8 TATA-box binding protein associated factor 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210422 MGI 1318182 Taf8 TATA-box binding protein associated factor 8 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20221103 MGI 1318182 Taf8 TATA-box binding protein associated factor 8 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 1318190 Garre1 granule associated Rac and RHOG effector 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1318194 1700123O20Rik RIKEN cDNA 1700123O20 gene gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20211021 MGI 1318196 Tor1b torsin family 1, member B gene MP:0001513 limb grasping IAGP N RGD:5509061 20210527 MGI PMID:32202496 1318196 Tor1b torsin family 1, member B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210527 MGI PMID:32202496 1318196 Tor1b torsin family 1, member B gene MP:0002083 premature death IAGP N RGD:5509061 20210527 MGI PMID:32202496 1318196 Tor1b torsin family 1, member B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210527 MGI PMID:32202496 1318196 Tor1b torsin family 1, member B gene MP:0002183 gliosis IAGP N RGD:5509061 20210527 MGI PMID:32202496 1318196 Tor1b torsin family 1, member B gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20210527 MGI PMID:32202496 1318196 Tor1b torsin family 1, member B gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20240523 MGI 1318196 Tor1b torsin family 1, member B gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20210527 MGI PMID:32202496 1318197 Mios meiosis regulator for oocyte development gene MP:0000774 decreased brain size IAGP N RGD:5509061 20220324 MGI PMID:35022234 1318197 Mios meiosis regulator for oocyte development gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20220324 MGI PMID:35022234 1318197 Mios meiosis regulator for oocyte development gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20220324 MGI PMID:35022234 1318197 Mios meiosis regulator for oocyte development gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20220324 MGI PMID:35022234 1318197 Mios meiosis regulator for oocyte development gene MP:0013438 dysmyelination IAGP N RGD:5509061 20220324 MGI PMID:35022234 1318202 Loxl2 lysyl oxidase-like 2 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20160519 MGI PMID:25759215 1318202 Loxl2 lysyl oxidase-like 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20160519 MGI PMID:25759215 1318202 Loxl2 lysyl oxidase-like 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20160519 MGI PMID:25759215 1318202 Loxl2 lysyl oxidase-like 2 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20160519 MGI PMID:25759215 1318202 Loxl2 lysyl oxidase-like 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20160519 MGI PMID:25759215 1318202 Loxl2 lysyl oxidase-like 2 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20160519 MGI PMID:25759215 1318202 Loxl2 lysyl oxidase-like 2 gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20160519 MGI PMID:25759215 1318202 Loxl2 lysyl oxidase-like 2 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20160519 MGI PMID:25759215 1318202 Loxl2 lysyl oxidase-like 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1318202 Loxl2 lysyl oxidase-like 2 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20160519 MGI PMID:25759215 1318209 Dgkq diacylglycerol kinase, theta gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1318209 Dgkq diacylglycerol kinase, theta gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1318209 Dgkq diacylglycerol kinase, theta gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 1318209 Dgkq diacylglycerol kinase, theta gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1318212 Lsm8 LSM8 homolog, U6 small nuclear RNA associated gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1318212 Lsm8 LSM8 homolog, U6 small nuclear RNA associated gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20210128 MGI 1318212 Lsm8 LSM8 homolog, U6 small nuclear RNA associated gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1318212 Lsm8 LSM8 homolog, U6 small nuclear RNA associated gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1318212 Lsm8 LSM8 homolog, U6 small nuclear RNA associated gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1318212 Lsm8 LSM8 homolog, U6 small nuclear RNA associated gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20231207 MGI 1318212 Lsm8 LSM8 homolog, U6 small nuclear RNA associated gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20231207 MGI 1318212 Lsm8 LSM8 homolog, U6 small nuclear RNA associated gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 1318212 Lsm8 LSM8 homolog, U6 small nuclear RNA associated gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20231207 MGI 1318212 Lsm8 LSM8 homolog, U6 small nuclear RNA associated gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318212 Lsm8 LSM8 homolog, U6 small nuclear RNA associated gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:18344997 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11526078 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:22056672 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:23494546 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:9584121 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21856296 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9584121 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:22056672 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:22056672 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:21856296 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:21856296 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22056672 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23996959 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:21856296 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0002711 decreased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:9584121 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:10217145 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:9584121 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:11076772 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:22056672 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:23494546 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:21856296 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0003647 absent oligodendrocytes IAGP N RGD:5509061 20141003 MGI PMID:11526078 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0003877 abnormal serotonergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10217145 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:10217145 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:9584121 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23494546 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:22056672 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0009174 absent pancreatic beta cells IAGP N RGD:5509061 20141003 MGI PMID:9584121 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22056672 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9584121 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:22056672 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:11076772 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:23494546 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:9584121 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0009186 decreased PP cell number IAGP N RGD:5509061 20141003 MGI PMID:11076772 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0009186 decreased PP cell number IAGP N RGD:5509061 20141003 MGI PMID:9584121 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0009190 increased pancreatic epsilon cell number IAGP N RGD:5509061 20141003 MGI PMID:22056672 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0009190 increased pancreatic epsilon cell number IAGP N RGD:5509061 20141003 MGI PMID:23494546 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:11076772 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:22056672 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11526078 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23494546 1318214 Nkx2-2 NK2 homeobox 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9584121 1318220 Rab25 RAB25, member RAS oncogene family gene MP:0000466 esophageal epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20197623 1318220 Rab25 RAB25, member RAS oncogene family gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:20197623 1318220 Rab25 RAB25, member RAS oncogene family gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:20197623 1318220 Rab25 RAB25, member RAS oncogene family gene MP:0001140 abnormal vagina epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20197623 1318220 Rab25 RAB25, member RAS oncogene family gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20197623 1318220 Rab25 RAB25, member RAS oncogene family gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20197623 1318220 Rab25 RAB25, member RAS oncogene family gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:20197623 1318220 Rab25 RAB25, member RAS oncogene family gene MP:0003276 esophageal atresia IAGP N RGD:5509061 20141003 MGI PMID:20197623 1318220 Rab25 RAB25, member RAS oncogene family gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20197623 1318223 Septin8 septin 8 gene MP:0000921 demyelination IAGP N RGD:5509061 20170629 MGI PMID:27504968 1318223 Septin8 septin 8 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1318223 Septin8 septin 8 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1318223 Septin8 septin 8 gene MP:0003313 abnormal locomotor activation IEA N RGD:5509061 20141003 MGI 1318223 Septin8 septin 8 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20170629 MGI PMID:27504968 1318223 Septin8 septin 8 gene MP:0012674 tomacula IAGP N RGD:5509061 20170629 MGI PMID:27504968 1318225 Sgo2a shugoshin 2A gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18765791 1318225 Sgo2a shugoshin 2A gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18765791 1318225 Sgo2a shugoshin 2A gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18765791 1318225 Sgo2a shugoshin 2A gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:18765791 1318225 Sgo2a shugoshin 2A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18765791 1318225 Sgo2a shugoshin 2A gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:18765791 1318225 Sgo2a shugoshin 2A gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:18765791 1318225 Sgo2a shugoshin 2A gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18765791 1318230 Rbx1 ring-box 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19325126 1318230 Rbx1 ring-box 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19325126 1318230 Rbx1 ring-box 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:19325126 1318230 Rbx1 ring-box 1 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:19325126 1318230 Rbx1 ring-box 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19325126 1318230 Rbx1 ring-box 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19325126 1318230 Rbx1 ring-box 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:19325126 1318233 Tmx1 thioredoxin-related transmembrane protein 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170406 MGI 1318235 Kirrel2 kirre like nephrin family adhesion molecule 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201022 MGI PMID:27430022 1318235 Kirrel2 kirre like nephrin family adhesion molecule 2 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20190425 MGI PMID:28815295 1318235 Kirrel2 kirre like nephrin family adhesion molecule 2 gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20190425 MGI PMID:28815295 1318235 Kirrel2 kirre like nephrin family adhesion molecule 2 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20190425 MGI PMID:28815295 1318235 Kirrel2 kirre like nephrin family adhesion molecule 2 gene MP:0020360 abnormal asymmetric synapse morphology IAGP N RGD:5509061 20190425 MGI PMID:28815295 1318237 Orc3 origin recognition complex, subunit 3 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21185282 1318237 Orc3 origin recognition complex, subunit 3 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20201231 MGI 1318237 Orc3 origin recognition complex, subunit 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318237 Orc3 origin recognition complex, subunit 3 gene MP:0020388 decreased radial glial cell number IAGP N RGD:5509061 20161117 MGI PMID:21185282 1318237 Orc3 origin recognition complex, subunit 3 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20161117 MGI PMID:21185282 1318241 Rnf149 ring finger protein 149 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20240613 MGI PMID:37031316 1318241 Rnf149 ring finger protein 149 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20240613 MGI PMID:37031316 1318241 Rnf149 ring finger protein 149 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20240613 MGI PMID:37031316 1318241 Rnf149 ring finger protein 149 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20240613 MGI PMID:37031316 1318241 Rnf149 ring finger protein 149 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20240613 MGI PMID:37031316 1318241 Rnf149 ring finger protein 149 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20240613 MGI PMID:37031316 1318242 Meak7 MTOR associated protein, eak-7 homolog gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20181227 MGI 1318242 Meak7 MTOR associated protein, eak-7 homolog gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1318242 Meak7 MTOR associated protein, eak-7 homolog gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20181227 MGI 1318247 Tcf15 transcription factor 15 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0000080 abnormal exoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0006295 absent sclerotome IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0008149 abnormal costovertebral joint morphology IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20171026 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0012248 absent dermatome IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318247 Tcf15 transcription factor 15 gene MP:0012249 absent myotome IAGP N RGD:5509061 20141003 MGI PMID:8955271 1318249 Cbln4 cerebellin 4 precursor protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22220752 1318251 Ctns cystinosis, nephropathic gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12370309 1318251 Ctns cystinosis, nephropathic gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12370309 1318251 Ctns cystinosis, nephropathic gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:12370309 1318251 Ctns cystinosis, nephropathic gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12370309 1318251 Ctns cystinosis, nephropathic gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12370309 1318251 Ctns cystinosis, nephropathic gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:12370309 1318251 Ctns cystinosis, nephropathic gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12370309 1318251 Ctns cystinosis, nephropathic gene MP:0005544 cornea deposits IAGP N RGD:5509061 20141003 MGI PMID:12370309 1318251 Ctns cystinosis, nephropathic gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12370309 1318251 Ctns cystinosis, nephropathic gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20141003 MGI PMID:12370309 1318251 Ctns cystinosis, nephropathic gene MP:0030622 increased cysteine level IAGP N RGD:5509061 20180920 MGI PMID:12370309 1318257 Gskip GSK3B interacting protein gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20160811 MGI PMID:26582204 1318257 Gskip GSK3B interacting protein gene MP:0001575 cyanosis IAGP N RGD:5509061 20160811 MGI PMID:26582204 1318257 Gskip GSK3B interacting protein gene MP:0001953 respiratory failure IAGP N RGD:5509061 20160811 MGI PMID:26582204 1318257 Gskip GSK3B interacting protein gene MP:0003717 pallor IAGP N RGD:5509061 20160811 MGI PMID:26582204 1318257 Gskip GSK3B interacting protein gene MP:0003756 abnormal hard palate morphology IAGP N RGD:5509061 20160811 MGI PMID:26582204 1318257 Gskip GSK3B interacting protein gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20160811 MGI PMID:26582204 1318257 Gskip GSK3B interacting protein gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20160811 MGI PMID:26582204 1318257 Gskip GSK3B interacting protein gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20160811 MGI PMID:26582204 1318257 Gskip GSK3B interacting protein gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160811 MGI PMID:26582204 1318257 Gskip GSK3B interacting protein gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20160811 MGI PMID:26582204 1318257 Gskip GSK3B interacting protein gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:26582204 1318257 Gskip GSK3B interacting protein gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:26582204 1318259 Mocs1 molybdenum cofactor synthesis 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12471057 1318259 Mocs1 molybdenum cofactor synthesis 1 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:12471057 1318259 Mocs1 molybdenum cofactor synthesis 1 gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:12471057 1318259 Mocs1 molybdenum cofactor synthesis 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:12471057 1318259 Mocs1 molybdenum cofactor synthesis 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12471057 1318259 Mocs1 molybdenum cofactor synthesis 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12471057 1318259 Mocs1 molybdenum cofactor synthesis 1 gene MP:0011424 decreased urine uric acid level IAGP N RGD:5509061 20230810 MGI PMID:12471057 1318259 Mocs1 molybdenum cofactor synthesis 1 gene MP:0020400 cystinuria IAGP N RGD:5509061 20161208 MGI PMID:12471057 1318259 Mocs1 molybdenum cofactor synthesis 1 gene MP:0020405 taurinuria IAGP N RGD:5509061 20161208 MGI PMID:12471057 1318259 Mocs1 molybdenum cofactor synthesis 1 gene MP:0031479 increased urine xanthine level IAGP N RGD:5509061 20230810 MGI PMID:12471057 1318260 Bbs9 Bardet-Biedl syndrome 9 gene MP:0001260 increased body weight IEA N RGD:5509061 20181011 MGI 1318260 Bbs9 Bardet-Biedl syndrome 9 gene MP:0002764 short tibia IEA N RGD:5509061 20181011 MGI 1318260 Bbs9 Bardet-Biedl syndrome 9 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20181011 MGI 1318260 Bbs9 Bardet-Biedl syndrome 9 gene MP:0014142 increased body fat mass IEA N RGD:5509061 20181011 MGI 1318262 Tpst1 protein-tyrosine sulfotransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11964405 1318262 Tpst1 protein-tyrosine sulfotransferase 1 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:11964405 1318262 Tpst1 protein-tyrosine sulfotransferase 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11964405 1318262 Tpst1 protein-tyrosine sulfotransferase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11964405 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16283626 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:10497154 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16283626 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0010178 increased number of Howell-Jolly bodies IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22910183 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10497154 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16283626 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0011180 abnormal hematopoietic cell number IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0011903 decreased hematopoietic stem cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24516162 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1318264 Mybl2 myeloblastosis oncogene-like 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20200220 MGI PMID:30600684 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:15830394 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17519956 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18782757 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:17519956 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20240111 MGI PMID:37584738 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18202188 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200220 MGI PMID:30600684 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002138 abnormal hepatobiliary system morphology IAGP N RGD:5509061 20141003 MGI PMID:18202188 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22021705 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18286309 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18782757 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:15830394 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:15830394 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20240111 MGI PMID:37584738 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22021705 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18286309 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20141003 MGI PMID:17519956 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20141003 MGI PMID:18286309 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20200220 MGI PMID:30600684 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20240111 MGI PMID:37584738 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003254 bile duct inflammation IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20141003 MGI PMID:17519956 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20141003 MGI PMID:18202188 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20200220 MGI PMID:30600684 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003266 biliary cyst IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003266 biliary cyst IAGP N RGD:5509061 20141003 MGI PMID:18202188 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003266 biliary cyst IAGP N RGD:5509061 20200220 MGI PMID:30600684 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003266 biliary cyst IAGP N RGD:5509061 20240111 MGI PMID:37584738 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003300 gastrointestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:15830394 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:17519956 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:18202188 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:22021705 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003327 liver cyst IAGP N RGD:5509061 20200220 MGI PMID:30600684 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003327 liver cyst IAGP N RGD:5509061 20240111 MGI PMID:37584738 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15830394 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17519956 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18202188 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18286309 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22021705 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200220 MGI PMID:30600684 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003334 pancreas fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18202188 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:17519956 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:18202188 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:18286309 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17519956 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18286309 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:22021705 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:22021705 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003946 renal necrosis IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20875407 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17519956 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0004967 abnormal kidney epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19959710 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0005083 abnormal biliary tract morphology IAGP N RGD:5509061 20240111 MGI PMID:37584738 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0005084 abnormal gallbladder morphology IAGP N RGD:5509061 20141003 MGI PMID:18286309 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:17519956 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:22021705 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20200220 MGI PMID:30600684 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0009143 abnormal pancreatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:17519956 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:17519956 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:18202188 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:18782757 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0009497 abnormal intrahepatic bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18286309 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0009498 abnormal extrahepatic bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18286309 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0009501 abnormal hepatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18286309 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:19959710 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17575307 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0011331 abnormal papillary duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0011352 proximal convoluted tubule brush border loss IAGP N RGD:5509061 20141003 MGI PMID:17519956 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0011359 decreased glomerular capillary number IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20875407 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:18235088 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:18286309 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0012238 abnormal cholangiocyte primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:17519956 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0013611 abnormal bile duct epithelium morphology IAGP N RGD:5509061 20240111 MGI PMID:37584738 1318267 Pkhd1 polycystic kidney and hepatic disease 1 gene MP:0014233 bile duct epithelium hyperplasia IAGP N RGD:5509061 20240111 MGI PMID:37584738 1318269 Drap1 DR1 associated protein 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:12471260 1318269 Drap1 DR1 associated protein 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:12471260 1318269 Drap1 DR1 associated protein 1 gene MP:0002174 abnormal gastrulation movements IAGP N RGD:5509061 20141003 MGI PMID:12471260 1318269 Drap1 DR1 associated protein 1 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:12471260 1318269 Drap1 DR1 associated protein 1 gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:12471260 1318269 Drap1 DR1 associated protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12471260 1318269 Drap1 DR1 associated protein 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12471260 1318269 Drap1 DR1 associated protein 1 gene MP:0012184 absent paraxial mesoderm IAGP N RGD:5509061 20141003 MGI PMID:12471260 1318269 Drap1 DR1 associated protein 1 gene MP:0012274 increased axial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:12471260 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20180322 MGI PMID:29415061 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20180201 MGI PMID:17284606 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20181122 MGI PMID:24768164 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:23434755 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20210401 MGI PMID:26489471 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20210401 MGI PMID:26489471 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20210121 MGI PMID:32783938 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20180201 MGI PMID:22281595 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20180201 MGI PMID:23434755 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20180322 MGI PMID:29415061 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000423 delayed hair regrowth IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000424 retarded hair growth IAGP N RGD:5509061 20180322 MGI PMID:29415061 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000469 abnormal esophageal squamous epithelium morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20210121 MGI PMID:32783938 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20210325 MGI PMID:26489471 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20180201 MGI PMID:26443207 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20221020 MGI PMID:35672775 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:22281595 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20221020 MGI PMID:35672775 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000649 sebaceous gland atrophy IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180201 MGI PMID:17284606 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20181122 MGI PMID:24768164 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20180322 MGI PMID:29415061 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000745 tremors IAGP N RGD:5509061 20180322 MGI PMID:29415061 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20180201 MGI PMID:26842965 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20220721 MGI PMID:35292640 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20221020 MGI PMID:35672775 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20180201 MGI PMID:25238791 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20180201 MGI PMID:25238791 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220721 MGI PMID:35292640 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001200 thick skin IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001221 epidermal atrophy IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20180201 MGI PMID:23666760 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:23300482 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:25238791 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210121 MGI PMID:32783938 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20221020 MGI PMID:35672775 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20181122 MGI PMID:24768164 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:23666760 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20180322 MGI PMID:29415061 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20221020 MGI PMID:35672775 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180201 MGI PMID:20534480 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180201 MGI PMID:20534480 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20221020 MGI PMID:35672775 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20220421 MGI PMID:26868444 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20220421 MGI PMID:26868444 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20220421 MGI PMID:26868444 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20180201 MGI PMID:20534480 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20180322 MGI PMID:29415061 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20180201 MGI PMID:17284606 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20180201 MGI PMID:17284606 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20180201 MGI PMID:22281595 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20180201 MGI PMID:26443207 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20210325 MGI PMID:26489471 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20210401 MGI PMID:26489471 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180201 MGI PMID:26443207 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20180201 MGI PMID:25198863 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20180201 MGI PMID:25198863 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180201 MGI PMID:25238791 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20220421 MGI PMID:26868444 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20201022 MGI PMID:32245620 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20201022 MGI PMID:32245620 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20221020 MGI PMID:35672775 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20201022 MGI PMID:32245620 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20221020 MGI PMID:35672775 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20180201 MGI PMID:20534480 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002006 neoplasm IAGP N RGD:5509061 20210121 MGI PMID:32783938 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002064 seizures IAGP N RGD:5509061 20180322 MGI PMID:29415061 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002064 seizures IAGP N RGD:5509061 20221020 MGI PMID:35672775 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20180201 MGI PMID:26443207 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20240328 MGI PMID:33807672 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:23300482 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:26443207 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20181122 MGI PMID:24768164 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20210121 MGI PMID:32783938 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20210325 MGI PMID:26489471 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20180201 MGI PMID:25198863 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20180201 MGI PMID:26443207 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20180927 MGI PMID:29999500 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20180201 MGI PMID:28207927 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20210325 MGI PMID:26489471 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20180201 MGI PMID:17284606 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20210401 MGI PMID:26489471 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20220421 MGI PMID:26868444 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20201022 MGI PMID:32245620 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20180201 MGI PMID:25238791 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20201022 MGI PMID:32245620 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20180201 MGI PMID:17284606 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20210401 MGI PMID:26489471 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:17284606 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:22281595 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20210401 MGI PMID:26489471 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20240328 MGI PMID:33807672 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20221020 MGI PMID:35672775 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20240328 MGI PMID:33807672 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003109 short femur IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20180201 MGI PMID:26443207 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20180201 MGI PMID:25198863 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003278 esophageal inflammation IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003380 abnormal intestine regeneration IAGP N RGD:5509061 20180201 MGI PMID:22956684 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20240328 MGI PMID:33807672 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003701 elevated level of mitotic sister chromatid exchange IAGP N RGD:5509061 20180201 MGI PMID:26443207 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20180201 MGI PMID:26443207 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003786 premature aging IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003786 premature aging IAGP N RGD:5509061 20180201 MGI PMID:26443207 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003846 matted coat IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:25238791 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20180201 MGI PMID:23300482 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180201 MGI PMID:25198863 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20180201 MGI PMID:26443207 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20210121 MGI PMID:32783938 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20211216 MGI PMID:32555289 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20180329 MGI PMID:29045572 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20210513 MGI PMID:32271880 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20210401 MGI PMID:26489471 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20240328 MGI PMID:33807672 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20180329 MGI PMID:29045572 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004627 abnormal trochanter morphology IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004675 rib fractures IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20180201 MGI PMID:23434755 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180201 MGI PMID:25238791 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20201022 MGI PMID:32245620 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220721 MGI PMID:35292640 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20221020 MGI PMID:35672775 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20201022 MGI PMID:32245620 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220721 MGI PMID:35292640 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20180201 MGI PMID:25198863 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004987 abnormal osteoblast cell number IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:23434755 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20181122 MGI PMID:24768164 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20180201 MGI PMID:22956684 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20180201 MGI PMID:25238791 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180201 MGI PMID:28655914 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20220721 MGI PMID:35292640 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20221020 MGI PMID:35672775 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20180201 MGI PMID:24949970 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240328 MGI PMID:33807672 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20221020 MGI PMID:35672775 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005397 hematopoietic system phenotype IAGP N RGD:5509061 20210121 MGI PMID:32783938 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20240328 MGI PMID:33807672 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20180201 MGI PMID:28207927 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20240328 MGI PMID:33807672 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20181122 MGI PMID:24768164 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20180201 MGI PMID:25198863 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220721 MGI PMID:35292640 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20180201 MGI PMID:23430111 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20180201 MGI PMID:23135404 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20180201 MGI PMID:23430111 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20180201 MGI PMID:23430111 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008615 decreased circulating interleukin-17 level IAGP N RGD:5509061 20180201 MGI PMID:22590468 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20180201 MGI PMID:25198863 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20210325 MGI PMID:26489471 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20210121 MGI PMID:32783938 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20180201 MGI PMID:17284606 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20180201 MGI PMID:23300482 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20180201 MGI PMID:21124450 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20180201 MGI PMID:22281595 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20180201 MGI PMID:23359070 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0009420 skeletal muscle endomysial fibrosis IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0009445 osteomalacia IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0009567 mitotic nondisjunction IAGP N RGD:5509061 20180201 MGI PMID:26443207 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0009635 enlarged popliteal lymph nodes IAGP N RGD:5509061 20180322 MGI PMID:29415061 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0009759 abnormal hair follicle bulge morphology IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0009794 sebaceous gland hyperplasia IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20180201 MGI PMID:23300482 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20180201 MGI PMID:26443207 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20240328 MGI PMID:33807672 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20181122 MGI PMID:24768164 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20180201 MGI PMID:23300482 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010537 tumor regression IAGP N RGD:5509061 20200423 MGI PMID:25208064 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010664 abnormal vitelline artery morphology IAGP N RGD:5509061 20180201 MGI PMID:25198863 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20210121 MGI PMID:32783938 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010862 decreased respiratory mucosa goblet cell number IAGP N RGD:5509061 20180201 MGI PMID:28207927 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20180201 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010897 abnormal bronchiole epithelium morphology IAGP N RGD:5509061 20180201 MGI PMID:25238791 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010901 abnormal pulmonary alveolar parenchyma morphology IAGP N RGD:5509061 20180201 MGI PMID:25238791 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010924 abnormal osteoid morphology IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20220721 MGI PMID:35292640 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20180201 MGI PMID:22590468 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0010965 decreased compact bone volume IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20180201 MGI PMID:23274892 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20210325 MGI PMID:26489471 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20180201 MGI PMID:22281595 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20180201 MGI PMID:18371340 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20180201 MGI PMID:25198863 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20210121 MGI PMID:32783938 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20240328 MGI PMID:33807672 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0012204 abnormal neuronal stem cell physiology IAGP N RGD:5509061 20200130 MGI PMID:31112699 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0012289 abnormal non-rapid eye movement sleep pattern IAGP N RGD:5509061 20220421 MGI PMID:26868444 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20181122 MGI PMID:24768164 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0013139 moribund IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0013288 premature acrosome reaction IAGP N RGD:5509061 20180329 MGI PMID:29045572 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20210121 MGI PMID:32783938 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0013585 thymus cortex atrophy IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0013586 thymus medulla atrophy IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20221020 MGI PMID:35672775 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0013626 decreased femur yield load IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0013633 decreased femur maximal load IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0013638 decreased femur stiffness IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0013646 decreased energy dissipated prior to femur fracture IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0013941 abnormal enthesis morphology IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20180201 MGI PMID:24949970 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20201022 MGI PMID:32245620 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220721 MGI PMID:35292640 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20180201 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20190221 MGI PMID:30254136 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0014344 abnormal skeletal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:24589777 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20180201 MGI PMID:28207927 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20180201 MGI PMID:28655914 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20221020 MGI PMID:35672775 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0020444 abnormal intestine apoptosis IAGP N RGD:5509061 20181122 MGI PMID:24768164 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0020478 abnormal circadian sleep/wake cycle IAGP N RGD:5509061 20220421 MGI PMID:26868444 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0030484 abnormal osteocyte lacuna morphology IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0030487 abnormal osteocyte dendritic process morphology IAGP N RGD:5509061 20180201 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0030827 femur fracture IAGP N RGD:5509061 20181018 MGI PMID:24419319 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:22505032 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20211118 MGI PMID:34566982 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240328 MGI PMID:33807672 1318272 Ndor1 NADPH dependent diflavin oxidoreductase 1 gene MP:0031392 hypoactivity IAGP N RGD:5509061 20220421 MGI PMID:26868444 1318275 Sdr42e1 short chain dehydrogenase/reductase family 42E, member 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20181227 MGI 1318275 Sdr42e1 short chain dehydrogenase/reductase family 42E, member 1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201231 MGI 1318277 Sfxn1 sideroflexin 1 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20220811 MGI 1318277 Sfxn1 sideroflexin 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1318277 Sfxn1 sideroflexin 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:12915479 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12915479 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12915479 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:12915479 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:12915479 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:12915479 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:12915479 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:12915479 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:12915479 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0003236 abnormal lens capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:12915479 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12915479 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0005286 decreased saturated fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:12915479 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12915479 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0008570 lipidosis IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:20060764 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12915479 1318279 Pex7 peroxisomal biogenesis factor 7 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:12915479 1318281 Triobp TRIO and F-actin binding protein gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 1318281 Triobp TRIO and F-actin binding protein gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210128 MGI 1318281 Triobp TRIO and F-actin binding protein gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:20510926 1318281 Triobp TRIO and F-actin binding protein gene MP:0004432 abnormal cochlear hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20510926 1318281 Triobp TRIO and F-actin binding protein gene MP:0004523 decreased cochlear hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:20510926 1318281 Triobp TRIO and F-actin binding protein gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:20510926 1318281 Triobp TRIO and F-actin binding protein gene MP:0004528 fused outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:20510926 1318281 Triobp TRIO and F-actin binding protein gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:20510926 1318281 Triobp TRIO and F-actin binding protein gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:20510926 1318281 Triobp TRIO and F-actin binding protein gene MP:0004589 abnormal cochlear hair cell development IAGP N RGD:5509061 20141003 MGI PMID:20510926 1318281 Triobp TRIO and F-actin binding protein gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1318281 Triobp TRIO and F-actin binding protein gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20220811 MGI 1318281 Triobp TRIO and F-actin binding protein gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:20510926 1318281 Triobp TRIO and F-actin binding protein gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1318281 Triobp TRIO and F-actin binding protein gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20510926 1318286 Dennd4c DENN domain containing 4C gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318286 Dennd4c DENN domain containing 4C gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318286 Dennd4c DENN domain containing 4C gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318286 Dennd4c DENN domain containing 4C gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318286 Dennd4c DENN domain containing 4C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318286 Dennd4c DENN domain containing 4C gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1318290 Nkd1 naked cuticle 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:15546883 1318290 Nkd1 naked cuticle 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15546883 1318290 Nkd1 naked cuticle 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:15546883 1318290 Nkd1 naked cuticle 1 gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:17438140 1318290 Nkd1 naked cuticle 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17438140 1318290 Nkd1 naked cuticle 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:17438140 1318290 Nkd1 naked cuticle 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15546883 1318290 Nkd1 naked cuticle 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17438140 1318290 Nkd1 naked cuticle 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15546883 1318290 Nkd1 naked cuticle 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15546883 1318290 Nkd1 naked cuticle 1 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:17438140 1318290 Nkd1 naked cuticle 1 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:17438140 1318296 Prdm5 PR domain containing 5 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22589746 1318296 Prdm5 PR domain containing 5 gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 1318296 Prdm5 PR domain containing 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1318296 Prdm5 PR domain containing 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1318296 Prdm5 PR domain containing 5 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22589746 1318296 Prdm5 PR domain containing 5 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1318296 Prdm5 PR domain containing 5 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:22589746 1318296 Prdm5 PR domain containing 5 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20181227 MGI 1318296 Prdm5 PR domain containing 5 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:22589746 1318296 Prdm5 PR domain containing 5 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:22589746 1318296 Prdm5 PR domain containing 5 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:22589746 1318296 Prdm5 PR domain containing 5 gene MP:0010965 decreased compact bone volume IAGP N RGD:5509061 20141003 MGI PMID:22589746 1318296 Prdm5 PR domain containing 5 gene MP:0011642 abnormal bone collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:22589746 1318296 Prdm5 PR domain containing 5 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:22589746 1318299 Kif20b kinesin family member 20B gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21214893 1318299 Kif20b kinesin family member 20B gene MP:0000111 cleft palate IAGP N RGD:5509061 20180830 MGI PMID:29208648 1318299 Kif20b kinesin family member 20B gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:21214893 1318299 Kif20b kinesin family member 20B gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:24173802 1318299 Kif20b kinesin family member 20B gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:21214893 1318299 Kif20b kinesin family member 20B gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:24173802 1318299 Kif20b kinesin family member 20B gene MP:0000433 microcephaly IAGP N RGD:5509061 20171221 MGI PMID:28359322 1318299 Kif20b kinesin family member 20B gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:21214893 1318299 Kif20b kinesin family member 20B gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:24173802 1318299 Kif20b kinesin family member 20B gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21214893 1318299 Kif20b kinesin family member 20B gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:21214893 1318299 Kif20b kinesin family member 20B gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:24173802 1318299 Kif20b kinesin family member 20B gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15755804 1318299 Kif20b kinesin family member 20B gene MP:0001293 anophthalmia IAGP N RGD:5509061 20180830 MGI PMID:29208648 1318299 Kif20b kinesin family member 20B gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:21214893 1318299 Kif20b kinesin family member 20B gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20171221 MGI PMID:28359322 1318299 Kif20b kinesin family member 20B gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:21214893 1318299 Kif20b kinesin family member 20B gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15755804 1318299 Kif20b kinesin family member 20B gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:21214893 1318299 Kif20b kinesin family member 20B gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24173802 1318299 Kif20b kinesin family member 20B gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:21214893 1318299 Kif20b kinesin family member 20B gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:21214893 1318299 Kif20b kinesin family member 20B gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20171221 MGI PMID:28359322 1318299 Kif20b kinesin family member 20B gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:24173802 1318299 Kif20b kinesin family member 20B gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20180830 MGI PMID:29208648 1318299 Kif20b kinesin family member 20B gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20171221 MGI PMID:28359322 1318299 Kif20b kinesin family member 20B gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:24173802 1318299 Kif20b kinesin family member 20B gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:24173802 1318299 Kif20b kinesin family member 20B gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20171221 MGI PMID:28359322 1318299 Kif20b kinesin family member 20B gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:24173802 1318299 Kif20b kinesin family member 20B gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20171221 MGI PMID:28359322 1318299 Kif20b kinesin family member 20B gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20171221 MGI PMID:28359322 1318299 Kif20b kinesin family member 20B gene MP:0008442 disorganized cortical plate IAGP N RGD:5509061 20171221 MGI PMID:28359322 1318299 Kif20b kinesin family member 20B gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:24173802 1318299 Kif20b kinesin family member 20B gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:21214893 1318299 Kif20b kinesin family member 20B gene MP:0010714 iris coloboma IAGP N RGD:5509061 20141003 MGI PMID:21214893 1318299 Kif20b kinesin family member 20B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21214893 1318299 Kif20b kinesin family member 20B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 1318299 Kif20b kinesin family member 20B gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:24173802 1318299 Kif20b kinesin family member 20B gene MP:0020337 abnormal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20171221 MGI PMID:28359322 1318299 Kif20b kinesin family member 20B gene MP:0020850 abnormal microtubule cytoskeleton morphology IAGP N RGD:5509061 20190718 MGI PMID:28359322 1318303 Sp5 trans-acting transcription factor 5 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11071760 1318303 Sp5 trans-acting transcription factor 5 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230601 MGI 1318303 Sp5 trans-acting transcription factor 5 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:11071760 1318303 Sp5 trans-acting transcription factor 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1318303 Sp5 trans-acting transcription factor 5 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:11071760 1318303 Sp5 trans-acting transcription factor 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11071760 1318303 Sp5 trans-acting transcription factor 5 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1318303 Sp5 trans-acting transcription factor 5 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1318303 Sp5 trans-acting transcription factor 5 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11071760 1318303 Sp5 trans-acting transcription factor 5 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1318303 Sp5 trans-acting transcription factor 5 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1318305 Rai1 retinoic acid induced 1 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20663924 1318305 Rai1 retinoic acid induced 1 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17517686 1318305 Rai1 retinoic acid induced 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0000413 polyphalangy IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:20663924 1318305 Rai1 retinoic acid induced 1 gene MP:0001261 obese IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17517686 1318305 Rai1 retinoic acid induced 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17024248 1318305 Rai1 retinoic acid induced 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17517686 1318305 Rai1 retinoic acid induced 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:20663924 1318305 Rai1 retinoic acid induced 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17517686 1318305 Rai1 retinoic acid induced 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17517686 1318305 Rai1 retinoic acid induced 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:17517686 1318305 Rai1 retinoic acid induced 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17517686 1318305 Rai1 retinoic acid induced 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:20663924 1318305 Rai1 retinoic acid induced 1 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:17517686 1318305 Rai1 retinoic acid induced 1 gene MP:0002083 premature death IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:17517686 1318305 Rai1 retinoic acid induced 1 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:17517686 1318305 Rai1 retinoic acid induced 1 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0004472 broad nasal bone IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:17517686 1318305 Rai1 retinoic acid induced 1 gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0005226 abnormal vertebral arch development IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:20663924 1318305 Rai1 retinoic acid induced 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0010701 fusion of atlas and odontoid process IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15746153 1318305 Rai1 retinoic acid induced 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:20663924 1318305 Rai1 retinoic acid induced 1 gene MP:0014124 increased amylin secretion IAGP N RGD:5509061 20160324 MGI PMID:20663924 1318305 Rai1 retinoic acid induced 1 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20170126 MGI PMID:27693255 1318305 Rai1 retinoic acid induced 1 gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20170202 MGI PMID:20663924 1318305 Rai1 retinoic acid induced 1 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:20663924 1318305 Rai1 retinoic acid induced 1 gene MP:0030189 broad snout IAGP N RGD:5509061 20171019 MGI PMID:15746153 1318309 Rbm38 RNA binding motif protein 38 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0001263 weight loss IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0001577 anemia IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0002083 premature death IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0003010 decreased mortality induced by ionizing radiation IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0003786 premature aging IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0012415 decreased sarcoma incidence IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20151015 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:25512531 1318309 Rbm38 RNA binding motif protein 38 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:25512531 1318312 Zfp462 zinc finger protein 462 gene MP:0000414 alopecia IAGP N RGD:5509061 20181004 MGI PMID:27621227 1318312 Zfp462 zinc finger protein 462 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20181004 MGI PMID:27621227 1318312 Zfp462 zinc finger protein 462 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20181004 MGI PMID:27621227 1318312 Zfp462 zinc finger protein 462 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20181004 MGI PMID:27621227 1318312 Zfp462 zinc finger protein 462 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20181004 MGI PMID:27621227 1318312 Zfp462 zinc finger protein 462 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1318312 Zfp462 zinc finger protein 462 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20220519 MGI 1318312 Zfp462 zinc finger protein 462 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20181004 MGI PMID:27621227 1318312 Zfp462 zinc finger protein 462 gene MP:0001785 edema IEA N RGD:5509061 20220519 MGI 1318312 Zfp462 zinc finger protein 462 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20181004 MGI PMID:27621227 1318312 Zfp462 zinc finger protein 462 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220519 MGI 1318312 Zfp462 zinc finger protein 462 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220519 MGI 1318312 Zfp462 zinc finger protein 462 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220519 MGI 1318312 Zfp462 zinc finger protein 462 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20181004 MGI PMID:27621227 1318312 Zfp462 zinc finger protein 462 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220519 MGI 1318312 Zfp462 zinc finger protein 462 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20181004 MGI PMID:27621227 1318312 Zfp462 zinc finger protein 462 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1318316 Arhgap5 Rho GTPase activating protein 5 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:12637587 1318316 Arhgap5 Rho GTPase activating protein 5 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12015964 1318316 Arhgap5 Rho GTPase activating protein 5 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:12015964 1318316 Arhgap5 Rho GTPase activating protein 5 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:12015964 1318316 Arhgap5 Rho GTPase activating protein 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12015964 1318316 Arhgap5 Rho GTPase activating protein 5 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:12015964 1318316 Arhgap5 Rho GTPase activating protein 5 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:12015964 1318316 Arhgap5 Rho GTPase activating protein 5 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:12705864 1318316 Arhgap5 Rho GTPase activating protein 5 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:12015964 1318316 Arhgap5 Rho GTPase activating protein 5 gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:12015964 1318316 Arhgap5 Rho GTPase activating protein 5 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12705864 1318316 Arhgap5 Rho GTPase activating protein 5 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12015964 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20190418 MGI PMID:30707697 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0000120 malocclusion IAGP N RGD:5509061 20190418 MGI PMID:30707697 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20190418 MGI PMID:30707697 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20201022 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20210520 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20170105 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0000445 short snout IAGP N RGD:5509061 20191212 MGI PMID:30707697 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20210715 MGI PMID:33899734 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0000852 small cerebellum IAGP N RGD:5509061 20210715 MGI PMID:33899734 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20210715 MGI PMID:33899734 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20210715 MGI PMID:33899734 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190418 MGI PMID:30707697 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0001314 cornea opacity IEA N RGD:5509061 20160211 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20181227 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20210715 MGI PMID:33899734 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0001925 male infertility IAGP N RGD:5509061 20190418 MGI PMID:30707697 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20190418 MGI PMID:30707697 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20201231 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20160114 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210715 MGI PMID:33899734 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160114 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20190418 MGI PMID:30707697 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20210715 MGI PMID:33899734 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20190418 MGI PMID:30707697 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0004471 short nasal bone IAGP N RGD:5509061 20190418 MGI PMID:30707697 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0004973 increased regulatory T cell number IEA N RGD:5509061 20201022 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20210715 MGI PMID:33899734 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20190418 MGI PMID:30707697 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20190418 MGI PMID:30707697 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0005505 thrombocytosis IEA N RGD:5509061 20210128 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160114 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0008119 decreased Langerhans cell number IEA N RGD:5509061 20201231 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0008211 decreased mature B cell number IEA N RGD:5509061 20201231 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0008862 asymmetric snout IAGP N RGD:5509061 20191212 MGI PMID:30707697 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160114 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IEA N RGD:5509061 20201022 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0010851 decreased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20210715 MGI PMID:33899734 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20210715 MGI PMID:33899734 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0013421 increased CD5-positive gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0013430 increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0013513 decreased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0013764 decreased T-helper cell number IEA N RGD:5509061 20201231 MGI 1318319 Hbs1l Hbs1-like (S. cerevisiae) gene MP:0020393 increased neuronal precursor proliferation IAGP N RGD:5509061 20210715 MGI PMID:33899734 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20160421 MGI 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0000745 tremors IEA N RGD:5509061 20201231 MGI 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:12890759 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:12890759 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17942483 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0001061 abnormal oculomotor nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12890759 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0001064 absent trochlear nerve IAGP N RGD:5509061 20141003 MGI PMID:12890759 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12890759 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0001304 cataract IEA N RGD:5509061 20170105 MGI 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0001488 increased startle reflex IEA N RGD:5509061 20201022 MGI 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0001513 limb grasping IEA N RGD:5509061 20160421 MGI 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20170525 MGI PMID:26319580 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:12890759 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:12890759 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:18434520 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0004082 abnormal habenula morphology IAGP N RGD:5509061 20141003 MGI PMID:12890759 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0004106 lymphatic vessel hyperplasia IAGP N RGD:5509061 20170525 MGI PMID:26319580 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0004222 iris synechia IEA N RGD:5509061 20240523 MGI 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:18434520 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:12890759 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:12890759 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0009945 abnormal accessory olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17942483 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0010197 abnormal lymphatic vessel endothelial cell morphology IAGP N RGD:5509061 20170525 MGI PMID:26319580 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0010368 abnormal lymphatic system physiology IAGP N RGD:5509061 20170525 MGI PMID:26319580 1318328 Sema3f sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1318330 Folr2 folate receptor beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10508523 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:17696610 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:17696610 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:17696610 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:17696610 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:17696610 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:20711356 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17696610 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20711356 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17696610 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20210128 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230601 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20211021 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210520 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210520 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:17696610 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:20711356 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201231 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20201231 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20181227 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:20711356 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230601 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:17696610 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20210520 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210128 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0005102 abnormal iris pigmentation IEA N RGD:5509061 20230601 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:17696610 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:20711356 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210520 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:17696610 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:17696610 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17696610 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:20711356 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20141003 MGI PMID:20711356 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20141003 MGI PMID:20711356 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:20711356 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20230601 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:17696610 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:20711356 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17696610 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20240523 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1318332 Trip13 thyroid hormone receptor interactor 13 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220714 MGI PMID:17696610 1318335 Ngly1 N-glycanase 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20210923 MGI PMID:34215698 1318335 Ngly1 N-glycanase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20170518 MGI PMID:25605922 1318335 Ngly1 N-glycanase 1 gene MP:0008762 embryonic lethality IEA N RGD:5509061 20160407 MGI 1318335 Ngly1 N-glycanase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210923 MGI PMID:34215698 1318335 Ngly1 N-glycanase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210923 MGI PMID:34215698 1318335 Ngly1 N-glycanase 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20210923 MGI PMID:34215698 1318337 Pold4 polymerase (DNA-directed), delta 4 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1318337 Pold4 polymerase (DNA-directed), delta 4 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1318337 Pold4 polymerase (DNA-directed), delta 4 gene MP:0001661 extended life span IAGP N RGD:5509061 20230119 MGI PMID:36356905 1318337 Pold4 polymerase (DNA-directed), delta 4 gene MP:0010266 decreased liver tumor incidence IAGP N RGD:5509061 20230119 MGI PMID:36356905 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20709292 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20709292 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:20709292 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:20709292 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:20709292 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0000706 small thymus IEA N RGD:5509061 20230119 MGI 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20709292 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230119 MGI 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20709292 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20709292 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20709292 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20709292 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20709292 1318339 Pglyrp4 peptidoglycan recognition protein 4 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20141003 MGI PMID:20709292 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:12141427 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:12141427 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000328 increased enterocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000478 delayed intestine development IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0002252 abnormal oropharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:12141427 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0002363 abnormal spleen marginal sinus morphology IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0002791 steatorrhea IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0004035 abnormal sublingual gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12141427 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0006400 decreased molar number IAGP N RGD:5509061 20141003 MGI PMID:12141427 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20150319 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008180 abnormal marginal zone B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008240 abnormal spleen marginal zone macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008241 abnormal metallophilic macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008241 abnormal metallophilic macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008471 abnormal spleen primary B follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:10790368 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0009477 small cecum IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10207146 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0013483 abnormal jejunum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20150319 MGI PMID:10926756 1318341 Nkx2-3 NK2 homeobox 3 gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20171221 MGI PMID:12141427 1318345 Ect2 ect2 oncogene gene MP:0000745 tremors IEA N RGD:5509061 20160421 MGI 1318345 Ect2 ect2 oncogene gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:22701760 1318345 Ect2 ect2 oncogene gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:22701760 1318345 Ect2 ect2 oncogene gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1318345 Ect2 ect2 oncogene gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160811 MGI 1318345 Ect2 ect2 oncogene gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12904583 1318345 Ect2 ect2 oncogene gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22701760 1318345 Ect2 ect2 oncogene gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318348 Cd5l CD5 antigen-like gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 1318348 Cd5l CD5 antigen-like gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20160421 MGI 1318348 Cd5l CD5 antigen-like gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:9892623 1318348 Cd5l CD5 antigen-like gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1318348 Cd5l CD5 antigen-like gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9892623 1318348 Cd5l CD5 antigen-like gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12598318 1318348 Cd5l CD5 antigen-like gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210805 MGI 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:17666404 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0002832 coarse hair IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0003099 retina detachment IAGP N RGD:5509061 20141003 MGI PMID:17664227 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0003385 abnormal body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0005114 premature hair loss IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0005155 herniated intestine IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17664227 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17666404 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17664227 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20141003 MGI PMID:17664227 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0006077 inguinal hernia IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0006238 abnormal choriocapillaris morphology IAGP N RGD:5509061 20141003 MGI PMID:17664227 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0008418 abnormal cutaneous elastic fiber morphology IAGP N RGD:5509061 20150129 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:17872905 1318352 Efemp1 epidermal growth factor-containing fibulin-like extracellular matrix protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1318354 Ttc4 tetratricopeptide repeat domain 4 gene MP:0001513 limb grasping IEA N RGD:5509061 20230601 MGI 1318354 Ttc4 tetratricopeptide repeat domain 4 gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20241010 MGI 1318354 Ttc4 tetratricopeptide repeat domain 4 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20241010 MGI 1318354 Ttc4 tetratricopeptide repeat domain 4 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241010 MGI 1318354 Ttc4 tetratricopeptide repeat domain 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1318354 Ttc4 tetratricopeptide repeat domain 4 gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20241010 MGI 1318356 Scand1 SCAN domain-containing 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1318356 Scand1 SCAN domain-containing 1 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20230601 MGI 1318356 Scand1 SCAN domain-containing 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230601 MGI 1318356 Scand1 SCAN domain-containing 1 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20230601 MGI 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000025 otic hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000087 absent mandible IAGP N RGD:5509061 20180705 MGI PMID:23469164 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000087 absent mandible IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12082638 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000441 increased cranium width IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20180705 MGI PMID:23469164 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:12082638 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12082638 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20180705 MGI PMID:23469164 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19074029 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:19074029 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:19074029 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19074029 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:19074029 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:19074029 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:19074029 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0000914 exencephaly IAGP N RGD:5509061 20240704 MGI PMID:38696583 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12082638 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19074029 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20180705 MGI PMID:23469164 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0001293 anophthalmia IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0001297 microphthalmia IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:12082638 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19074029 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12082638 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:12082638 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19074029 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12082638 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0002234 abnormal pharynx morphology IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12082638 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:19074029 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0003051 curly tail IAGP N RGD:5509061 20240704 MGI PMID:38696583 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0003421 abnormal thyroid gland development IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0003923 abnormal heart left atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0004062 dilated heart right atrium IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0004380 short frontal bone IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0004461 basisphenoid bone hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20180705 MGI PMID:23469164 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0005163 cyclopia IAGP N RGD:5509061 20180705 MGI PMID:23469164 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0005163 cyclopia IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20180705 MGI PMID:23469164 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0006290 proboscis IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:19074029 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19074029 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19074029 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0009880 decreased mouth size IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0009905 absent tongue IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0009929 meningomyelocele IAGP N RGD:5509061 20240704 MGI PMID:38696583 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19074029 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12082638 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12082638 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12082638 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12082638 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0013573 abnormal parathyroid gland development IAGP N RGD:5509061 20150305 MGI PMID:11242111 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0013818 abnormal oral cavity morphology IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0030160 abnormal auditory bulla morphology IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318358 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like gene MP:0031463 increased palatal shelf size IAGP N RGD:5509061 20230309 MGI PMID:25565927 1318360 Meis3 Meis homeobox 3 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20220519 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0000601 small liver IEA N RGD:5509061 20220519 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20220519 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220519 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0011045 decreased lung elastance IEA N RGD:5509061 20221215 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0011048 decreased lung tissue damping IEA N RGD:5509061 20221215 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0011625 cystolithiasis IEA N RGD:5509061 20220519 MGI 1318360 Meis3 Meis homeobox 3 gene MP:0013129 abnormal tooth color IEA N RGD:5509061 20220519 MGI 1318363 Rtbdn retbindin gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1318363 Rtbdn retbindin gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20201231 MGI 1318363 Rtbdn retbindin gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20191024 MGI PMID:29079576 1318363 Rtbdn retbindin gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20191024 MGI PMID:29079576 1318363 Rtbdn retbindin gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20191024 MGI PMID:29079576 1318363 Rtbdn retbindin gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 1318363 Rtbdn retbindin gene MP:0005505 thrombocytosis IEA N RGD:5509061 20150108 MGI 1318363 Rtbdn retbindin gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20191024 MGI PMID:29079576 1318363 Rtbdn retbindin gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20191024 MGI PMID:29079576 1318363 Rtbdn retbindin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20191024 MGI PMID:29079576 1318363 Rtbdn retbindin gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20191024 MGI PMID:29079576 1318363 Rtbdn retbindin gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20191024 MGI PMID:29079576 1318363 Rtbdn retbindin gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20191024 MGI PMID:29079576 1318366 Coch cochlin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14657014 1318366 Coch cochlin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16481359 1318366 Coch cochlin gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:18697796 1318366 Coch cochlin gene MP:0004814 reduced linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:18697796 1318366 Coch cochlin gene MP:0004814 reduced linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:21073934 1318366 Coch cochlin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18697796 1318366 Coch cochlin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21073934 1318371 Kif5c kinesin family member 5C gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:10964943 1318371 Kif5c kinesin family member 5C gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:10964943 1318371 Kif5c kinesin family member 5C gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1318371 Kif5c kinesin family member 5C gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20230601 MGI 1318371 Kif5c kinesin family member 5C gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20230601 MGI 1318371 Kif5c kinesin family member 5C gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20230601 MGI 1318371 Kif5c kinesin family member 5C gene MP:0006006 increased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:10964943 1318371 Kif5c kinesin family member 5C gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20141003 MGI PMID:21335237 1318372 Utp3 UTP3 small subunit processome component gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20220915 MGI PMID:35328065 1318372 Utp3 UTP3 small subunit processome component gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20220915 MGI PMID:35328065 1318372 Utp3 UTP3 small subunit processome component gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20220915 MGI PMID:35328065 1318375 Sirt1 sirtuin 1 gene MP:0000149 abnormal scapula morphology IEA N RGD:5509061 20201231 MGI 1318375 Sirt1 sirtuin 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20170713 MGI PMID:28273169 1318375 Sirt1 sirtuin 1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201022 MGI 1318375 Sirt1 sirtuin 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0000445 short snout IAGP N RGD:5509061 20170713 MGI PMID:28273169 1318375 Sirt1 sirtuin 1 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20201022 MGI 1318375 Sirt1 sirtuin 1 gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20170713 MGI PMID:28273169 1318375 Sirt1 sirtuin 1 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17201918 1318375 Sirt1 sirtuin 1 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:17201918 1318375 Sirt1 sirtuin 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:20008932 1318375 Sirt1 sirtuin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17201918 1318375 Sirt1 sirtuin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17877786 1318375 Sirt1 sirtuin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20008932 1318375 Sirt1 sirtuin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17877786 1318375 Sirt1 sirtuin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20668205 1318375 Sirt1 sirtuin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170713 MGI PMID:28273169 1318375 Sirt1 sirtuin 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20201022 MGI 1318375 Sirt1 sirtuin 1 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20170713 MGI PMID:28273169 1318375 Sirt1 sirtuin 1 gene MP:0001346 abnormal lacrimal gland morphology IAGP N RGD:5509061 20170713 MGI PMID:28273169 1318375 Sirt1 sirtuin 1 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20008932 1318375 Sirt1 sirtuin 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18335035 1318375 Sirt1 sirtuin 1 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:18687325 1318375 Sirt1 sirtuin 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:18335035 1318375 Sirt1 sirtuin 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21103071 1318375 Sirt1 sirtuin 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21103071 1318375 Sirt1 sirtuin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17201918 1318375 Sirt1 sirtuin 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20170713 MGI PMID:28273169 1318375 Sirt1 sirtuin 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17877786 1318375 Sirt1 sirtuin 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20170713 MGI PMID:28273169 1318375 Sirt1 sirtuin 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17877786 1318375 Sirt1 sirtuin 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20170713 MGI PMID:28273169 1318375 Sirt1 sirtuin 1 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20170713 MGI PMID:28273169 1318375 Sirt1 sirtuin 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17201918 1318375 Sirt1 sirtuin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20201022 MGI 1318375 Sirt1 sirtuin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17201918 1318375 Sirt1 sirtuin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 1318375 Sirt1 sirtuin 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:18335035 1318375 Sirt1 sirtuin 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:18687325 1318375 Sirt1 sirtuin 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1318375 Sirt1 sirtuin 1 gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:21103071 1318375 Sirt1 sirtuin 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20008932 1318375 Sirt1 sirtuin 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:18687325 1318375 Sirt1 sirtuin 1 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20008932 1318375 Sirt1 sirtuin 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:18687325 1318375 Sirt1 sirtuin 1 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:18335035 1318375 Sirt1 sirtuin 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20170713 MGI PMID:28273169 1318375 Sirt1 sirtuin 1 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20141003 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20211021 MGI 1318375 Sirt1 sirtuin 1 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20201231 MGI 1318375 Sirt1 sirtuin 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:20008932 1318375 Sirt1 sirtuin 1 gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:18687325 1318375 Sirt1 sirtuin 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:20008932 1318375 Sirt1 sirtuin 1 gene MP:0005124 increased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:20008932 1318375 Sirt1 sirtuin 1 gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20141003 MGI PMID:17877786 1318375 Sirt1 sirtuin 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20170713 MGI PMID:28273169 1318375 Sirt1 sirtuin 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0005287 narrow eye opening IEA N RGD:5509061 20201022 MGI 1318375 Sirt1 sirtuin 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:18335035 1318375 Sirt1 sirtuin 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18335035 1318375 Sirt1 sirtuin 1 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20008932 1318375 Sirt1 sirtuin 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:18687325 1318375 Sirt1 sirtuin 1 gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18335035 1318375 Sirt1 sirtuin 1 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:20008932 1318375 Sirt1 sirtuin 1 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:20008932 1318375 Sirt1 sirtuin 1 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:18335035 1318375 Sirt1 sirtuin 1 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20008932 1318375 Sirt1 sirtuin 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:20008932 1318375 Sirt1 sirtuin 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20161103 MGI PMID:26074075 1318375 Sirt1 sirtuin 1 gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20170713 MGI PMID:28273169 1318375 Sirt1 sirtuin 1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:17201918 1318375 Sirt1 sirtuin 1 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18335035 1318375 Sirt1 sirtuin 1 gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0008938 decreased pituitary gland weight IAGP N RGD:5509061 20141003 MGI PMID:20008932 1318375 Sirt1 sirtuin 1 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0009081 thin uterus IAGP N RGD:5509061 20220714 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0009164 exocrine pancreas atrophy IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21103071 1318375 Sirt1 sirtuin 1 gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20170713 MGI PMID:28273169 1318375 Sirt1 sirtuin 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0010946 hyperpnea IAGP N RGD:5509061 20170713 MGI PMID:28273169 1318375 Sirt1 sirtuin 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:18335035 1318375 Sirt1 sirtuin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17201918 1318375 Sirt1 sirtuin 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12960381 1318375 Sirt1 sirtuin 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17201918 1318375 Sirt1 sirtuin 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1318375 Sirt1 sirtuin 1 gene MP:0011543 increased urine antidiuretic hormone level IAGP N RGD:5509061 20141003 MGI PMID:18687325 1318375 Sirt1 sirtuin 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:22006156 1318375 Sirt1 sirtuin 1 gene MP:0012298 hypoactivity in response to feed restriction IAGP N RGD:5509061 20141003 MGI PMID:20668205 1318375 Sirt1 sirtuin 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0013168 absent hindlimb buds IAGP N RGD:5509061 20150528 MGI PMID:18835033 1318375 Sirt1 sirtuin 1 gene MP:0013604 abnormal adult Leydig cell differentiation IAGP N RGD:5509061 20150319 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0013716 hypolactation IAGP N RGD:5509061 20150611 MGI PMID:17201918 1318375 Sirt1 sirtuin 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0014269 decreased testes secretion IAGP N RGD:5509061 20230810 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:18687325 1318375 Sirt1 sirtuin 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:18987333 1318375 Sirt1 sirtuin 1 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220714 MGI PMID:12482959 1318375 Sirt1 sirtuin 1 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220714 MGI PMID:22006156 1318377 Pura purine rich element binding protein A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:22010047 1318377 Pura purine rich element binding protein A gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:22010047 1318377 Pura purine rich element binding protein A gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:22010047 1318377 Pura purine rich element binding protein A gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:22010047 1318377 Pura purine rich element binding protein A gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22010047 1318377 Pura purine rich element binding protein A gene MP:0001391 abnormal tail movements IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22010047 1318377 Pura purine rich element binding protein A gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22010047 1318377 Pura purine rich element binding protein A gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:22010047 1318377 Pura purine rich element binding protein A gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:22010047 1318377 Pura purine rich element binding protein A gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22010047 1318377 Pura purine rich element binding protein A gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:22010047 1318377 Pura purine rich element binding protein A gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:22010047 1318377 Pura purine rich element binding protein A gene MP:0010897 abnormal bronchiole epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22010047 1318377 Pura purine rich element binding protein A gene MP:0011149 abnormal hippocampus stratum lacunosum morphology IAGP N RGD:5509061 20141003 MGI PMID:22010047 1318377 Pura purine rich element binding protein A gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20220310 MGI PMID:12972605 1318377 Pura purine rich element binding protein A gene MP:0021086 decreased DNA replication IAGP N RGD:5509061 20220310 MGI PMID:12972605 1318378 Cfap90 cilia and flagella associated protein 90 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38697008 1318380 Zfp422 zinc finger protein 422 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1318380 Zfp422 zinc finger protein 422 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1318380 Zfp422 zinc finger protein 422 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1318380 Zfp422 zinc finger protein 422 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1318380 Zfp422 zinc finger protein 422 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1318380 Zfp422 zinc finger protein 422 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20201217 MGI PMID:31685980 1318380 Zfp422 zinc finger protein 422 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 1318380 Zfp422 zinc finger protein 422 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20201217 MGI PMID:31685980 1318380 Zfp422 zinc finger protein 422 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20201217 MGI PMID:31685980 1318380 Zfp422 zinc finger protein 422 gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20201217 MGI PMID:31685980 1318380 Zfp422 zinc finger protein 422 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20201217 MGI PMID:31685980 1318383 Crygn crystallin, gamma N gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20170713 MGI PMID:27517863 1318383 Crygn crystallin, gamma N gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210520 MGI 1318383 Crygn crystallin, gamma N gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20170713 MGI PMID:27517863 1318383 Crygn crystallin, gamma N gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20170713 MGI PMID:27517863 1318385 Dhx9 DExH-box helicase 9 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:9811865 1318385 Dhx9 DExH-box helicase 9 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:9811865 1318385 Dhx9 DExH-box helicase 9 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9811865 1318385 Dhx9 DExH-box helicase 9 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:9811865 1318385 Dhx9 DExH-box helicase 9 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22988576 1318385 Dhx9 DExH-box helicase 9 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:9811865 1318385 Dhx9 DExH-box helicase 9 gene MP:0003895 increased ectoderm apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9811865 1318385 Dhx9 DExH-box helicase 9 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:9811865 1318385 Dhx9 DExH-box helicase 9 gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:9811865 1318385 Dhx9 DExH-box helicase 9 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20240523 MGI 1318385 Dhx9 DExH-box helicase 9 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20240523 MGI 1318385 Dhx9 DExH-box helicase 9 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22988576 1318385 Dhx9 DExH-box helicase 9 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9811865 1318385 Dhx9 DExH-box helicase 9 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9811865 1318385 Dhx9 DExH-box helicase 9 gene MP:0011187 abnormal parietal endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9811865 1318385 Dhx9 DExH-box helicase 9 gene MP:0011940 decreased food intake IEA N RGD:5509061 20240523 MGI 1318385 Dhx9 DExH-box helicase 9 gene MP:0012105 delayed gastrulation IAGP N RGD:5509061 20141003 MGI PMID:9811865 1318385 Dhx9 DExH-box helicase 9 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:9811865 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20170119 MGI PMID:27748972 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20170119 MGI PMID:27748972 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0001393 ataxia IAGP N RGD:5509061 20170119 MGI PMID:27748972 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0001785 edema IAGP N RGD:5509061 20170119 MGI PMID:27748972 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0002176 increased brain weight IAGP N RGD:5509061 20180111 MGI PMID:25382142 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20170119 MGI PMID:27748972 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20180111 MGI PMID:25382142 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20190425 MGI PMID:28695146 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0003354 astrocytosis IAGP N RGD:5509061 20170119 MGI PMID:27748972 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20150827 MGI PMID:24647135 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20150827 MGI PMID:24647135 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20170119 MGI PMID:27748972 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20180111 MGI PMID:25382142 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0005238 increased brain size IAGP N RGD:5509061 20180111 MGI PMID:25382142 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20150827 MGI PMID:24647135 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20170119 MGI PMID:27748972 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20180111 MGI PMID:25382142 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20190425 MGI PMID:28695146 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20170119 MGI PMID:27748972 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20170119 MGI PMID:27748972 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20180111 MGI PMID:25382142 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20150827 MGI PMID:24647135 1318393 Mlc1 megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) gene MP:0011854 cerebral edema IAGP N RGD:5509061 20180111 MGI PMID:25382142 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20210318 MGI PMID:27677211 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20181227 MGI 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20210318 MGI PMID:27677211 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20210318 MGI PMID:27677211 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20181227 MGI 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210318 MGI PMID:27677211 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210318 MGI PMID:27677211 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210318 MGI PMID:27677211 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20180412 MGI PMID:25126785 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210318 MGI PMID:27677211 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210318 MGI PMID:27677211 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0009235 small sperm head IAGP N RGD:5509061 20210318 MGI PMID:27677211 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20210318 MGI PMID:27677211 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0009325 necrospermia IAGP N RGD:5509061 20210318 MGI PMID:27677211 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20210318 MGI PMID:27677211 1318395 Kcng4 potassium voltage-gated channel, subfamily G, member 4 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210318 MGI PMID:27677211 1318397 Lca5 Leber congenital amaurosis 5 (human) gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21606596 1318397 Lca5 Leber congenital amaurosis 5 (human) gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21606596 1318397 Lca5 Leber congenital amaurosis 5 (human) gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21606596 1318397 Lca5 Leber congenital amaurosis 5 (human) gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21606596 1318397 Lca5 Leber congenital amaurosis 5 (human) gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21606596 1318397 Lca5 Leber congenital amaurosis 5 (human) gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:21606596 1318397 Lca5 Leber congenital amaurosis 5 (human) gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:21606596 1318397 Lca5 Leber congenital amaurosis 5 (human) gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:21606596 1318397 Lca5 Leber congenital amaurosis 5 (human) gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:21606596 1318398 Sppl2b signal peptide peptidase like 2B gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20151217 MGI PMID:24492962 1318398 Sppl2b signal peptide peptidase like 2B gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20151217 MGI PMID:24492962 1318398 Sppl2b signal peptide peptidase like 2B gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20151217 MGI PMID:24492962 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0000746 weakness IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0001785 edema IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0003653 decreased skin turgor IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318401 Rap1gds1 RAP1, GTP-GDP dissociation stimulator 1 gene MP:0013182 increased spinal cord apoptosis IAGP N RGD:5509061 20201231 MGI PMID:10793158 1318404 Nkiras1 NFKB inhibitor interacting Ras-like protein 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20240523 MGI 1318404 Nkiras1 NFKB inhibitor interacting Ras-like protein 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 1318404 Nkiras1 NFKB inhibitor interacting Ras-like protein 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11254677 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11254677 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:10843382 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:11254677 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:17392163 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:19305396 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:10843382 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:10843382 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11254677 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17694574 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:19662682 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19662682 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10843382 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16713979 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17392163 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11254677 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:10843382 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002392 abnormal Peyer's patch T cell area morphology IAGP N RGD:5509061 20141003 MGI PMID:16713979 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18258848 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19305396 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18504307 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12928364 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17615242 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17694574 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17392163 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11514610 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10843382 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19305396 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:19305396 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:17694574 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10843382 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17392163 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19305396 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10843382 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210826 MGI 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12928364 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11254677 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19305396 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19662682 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11514610 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0006173 abnormal myeloid dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11254677 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0006173 abnormal myeloid dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17694574 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19305396 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19305396 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:17392163 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008197 abnormal follicular dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16713979 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008198 abnormal follicular dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:16713979 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008244 abnormal peritoneal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:17694574 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008399 abnormal alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12928364 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008400 abnormal CD4-positive, alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12928364 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008401 abnormal CD8 positive, alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12928364 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:10843382 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17694574 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18258848 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18258848 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:19662682 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:17694574 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:17694574 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:18258848 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:18258848 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:11514610 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:11514610 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0008895 abnormal intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:10843382 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210826 MGI 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0011077 decreased macrophage nitric oxide production IAGP N RGD:5509061 20141003 MGI PMID:17694574 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20141003 MGI PMID:17694574 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0014472 impaired B cell migration IAGP N RGD:5509061 20240613 MGI PMID:17392163 1318407 Ccr6 C-C motif chemokine receptor 6 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:10843382 1318419 L3mbtl2 L3MBTL2 polycomb repressive complex 1 subunit gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20161216 MGI PMID:22770845 1318419 L3mbtl2 L3MBTL2 polycomb repressive complex 1 subunit gene MP:0003036 vertebral transformation IEA N RGD:5509061 20150430 MGI 1318419 L3mbtl2 L3MBTL2 polycomb repressive complex 1 subunit gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20161216 MGI PMID:22770845 1318419 L3mbtl2 L3MBTL2 polycomb repressive complex 1 subunit gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20161216 MGI PMID:22770845 1318419 L3mbtl2 L3MBTL2 polycomb repressive complex 1 subunit gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318419 L3mbtl2 L3MBTL2 polycomb repressive complex 1 subunit gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20161216 MGI PMID:22770845 1318419 L3mbtl2 L3MBTL2 polycomb repressive complex 1 subunit gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318419 L3mbtl2 L3MBTL2 polycomb repressive complex 1 subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318419 L3mbtl2 L3MBTL2 polycomb repressive complex 1 subunit gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318421 Atad1 ATPase family, AAA domain containing 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21496646 1318421 Atad1 ATPase family, AAA domain containing 1 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:21496646 1318421 Atad1 ATPase family, AAA domain containing 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:21496646 1318421 Atad1 ATPase family, AAA domain containing 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21496646 1318421 Atad1 ATPase family, AAA domain containing 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21496646 1318421 Atad1 ATPase family, AAA domain containing 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:21496646 1318421 Atad1 ATPase family, AAA domain containing 1 gene MP:0008431 abnormal short-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:21496646 1318421 Atad1 ATPase family, AAA domain containing 1 gene MP:0011002 enhanced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21496646 1318421 Atad1 ATPase family, AAA domain containing 1 gene MP:0014373 increased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:21496646 1318428 Cldn8 claudin 8 gene MP:0001596 hypotension IAGP N RGD:5509061 20161027 MGI PMID:25831548 1318428 Cldn8 claudin 8 gene MP:0001762 polyuria IAGP N RGD:5509061 20161027 MGI PMID:25831548 1318428 Cldn8 claudin 8 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20161027 MGI PMID:25831548 1318428 Cldn8 claudin 8 gene MP:0003016 increased circulating bicarbonate level IAGP N RGD:5509061 20161027 MGI PMID:25831548 1318428 Cldn8 claudin 8 gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20161027 MGI PMID:25831548 1318428 Cldn8 claudin 8 gene MP:0003028 alkalosis IAGP N RGD:5509061 20161027 MGI PMID:25831548 1318428 Cldn8 claudin 8 gene MP:0004119 hypokalemia IAGP N RGD:5509061 20161027 MGI PMID:25831548 1318428 Cldn8 claudin 8 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20161027 MGI PMID:25831548 1318428 Cldn8 claudin 8 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20161027 MGI PMID:25831548 1318428 Cldn8 claudin 8 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20161027 MGI PMID:25831548 1318428 Cldn8 claudin 8 gene MP:0005628 decreased circulating potassium level IAGP N RGD:5509061 20161027 MGI PMID:25831548 1318428 Cldn8 claudin 8 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20161027 MGI PMID:25831548 1318428 Cldn8 claudin 8 gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20161027 MGI PMID:25831548 1318433 Osgep O-sialoglycoprotein endopeptidase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1318435 H3c2 H3 clustered histone 2 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20200521 MGI PMID:32142668 1318435 H3c2 H3 clustered histone 2 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20200521 MGI PMID:32142668 1318435 H3c2 H3 clustered histone 2 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20200521 MGI PMID:32142668 1318435 H3c2 H3 clustered histone 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200521 MGI PMID:32142668 1318436 Dipk1a divergent protein kinase domain 1A gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1318436 Dipk1a divergent protein kinase domain 1A gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20170105 MGI 1318436 Dipk1a divergent protein kinase domain 1A gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 1318436 Dipk1a divergent protein kinase domain 1A gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1318436 Dipk1a divergent protein kinase domain 1A gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1318438 Shmt2 serine hydroxymethyltransferase 2 (mitochondrial) gene MP:0001577 anemia IAGP N RGD:5509061 20180503 MGI PMID:29323231 1318438 Shmt2 serine hydroxymethyltransferase 2 (mitochondrial) gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200402 MGI 1318438 Shmt2 serine hydroxymethyltransferase 2 (mitochondrial) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180503 MGI PMID:29323231 1318438 Shmt2 serine hydroxymethyltransferase 2 (mitochondrial) gene MP:0002080 prenatal lethality IEA N RGD:5509061 20201231 MGI 1318438 Shmt2 serine hydroxymethyltransferase 2 (mitochondrial) gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1318438 Shmt2 serine hydroxymethyltransferase 2 (mitochondrial) gene MP:0003896 prolonged PR interval IEA N RGD:5509061 20221215 MGI 1318438 Shmt2 serine hydroxymethyltransferase 2 (mitochondrial) gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20200402 MGI 1318438 Shmt2 serine hydroxymethyltransferase 2 (mitochondrial) gene MP:0004952 increased spleen weight IEA N RGD:5509061 20220811 MGI 1318438 Shmt2 serine hydroxymethyltransferase 2 (mitochondrial) gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20180503 MGI PMID:29323231 1318438 Shmt2 serine hydroxymethyltransferase 2 (mitochondrial) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180503 MGI PMID:29323231 1318438 Shmt2 serine hydroxymethyltransferase 2 (mitochondrial) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318438 Shmt2 serine hydroxymethyltransferase 2 (mitochondrial) gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20180503 MGI PMID:29323231 1318444 Oasl1 2'-5' oligoadenylate synthetase-like 1 gene MP:0008548 abnormal circulating interferon level IAGP N RGD:5509061 20141003 MGI PMID:23416614 1318444 Oasl1 2'-5' oligoadenylate synthetase-like 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1318444 Oasl1 2'-5' oligoadenylate synthetase-like 1 gene MP:0020938 decreased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200514 MGI PMID:23416614 1318444 Oasl1 2'-5' oligoadenylate synthetase-like 1 gene MP:0031039 decreased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:23416614 1318446 Slc37a1 solute carrier family 37 (glycerol-3-phosphate transporter), member 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1318446 Slc37a1 solute carrier family 37 (glycerol-3-phosphate transporter), member 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20181227 MGI 1318446 Slc37a1 solute carrier family 37 (glycerol-3-phosphate transporter), member 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1318446 Slc37a1 solute carrier family 37 (glycerol-3-phosphate transporter), member 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1318446 Slc37a1 solute carrier family 37 (glycerol-3-phosphate transporter), member 1 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20210128 MGI 1318448 Loxl4 lysyl oxidase-like 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 1318448 Loxl4 lysyl oxidase-like 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1318450 Il18r1 interleukin 18 receptor 1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:10227969 1318450 Il18r1 interleukin 18 receptor 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220811 MGI 1318450 Il18r1 interleukin 18 receptor 1 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:10227969 1318450 Il18r1 interleukin 18 receptor 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10227969 1318450 Il18r1 interleukin 18 receptor 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:24176642 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:24176642 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:24176642 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0004569 glossopharyngeal nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23934123 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:24176642 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:24176642 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:24176642 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:24176642 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0009879 abnormal arcus anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16951254 1318454 Tasp1 taspase, threonine aspartase 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:24176642 1318461 Kif23 kinesin family member 23 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230914 MGI PMID:32818800 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20170105 MGI PMID:26123588 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20220804 MGI PMID:35472723 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20170105 MGI PMID:26123588 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170105 MGI PMID:26123588 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20220804 MGI PMID:35472723 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20220804 MGI PMID:35472723 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20220804 MGI PMID:35472723 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0005039 hypoxia IAGP N RGD:5509061 20180111 MGI PMID:28204537 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20220804 MGI PMID:35472723 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20220804 MGI PMID:35472723 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0005563 abnormal hemoglobin content IAGP N RGD:5509061 20180111 MGI PMID:28204537 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20220804 MGI PMID:35472723 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0010147 abnormal endocrine pancreas physiology IAGP N RGD:5509061 20220804 MGI PMID:35472723 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20220804 MGI PMID:35472723 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20220804 MGI PMID:35472723 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20170105 MGI PMID:26123588 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318464 Sdhb succinate dehydrogenase complex, subunit B, iron sulfur (Ip) gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20220804 MGI PMID:35472723 1318468 Ark2n arkadia (RNF111) N-terminal like PKA signaling regulator 2N gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20221201 MGI PMID:35882232 1318468 Ark2n arkadia (RNF111) N-terminal like PKA signaling regulator 2N gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20221201 MGI PMID:35882232 1318468 Ark2n arkadia (RNF111) N-terminal like PKA signaling regulator 2N gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20221201 MGI PMID:35882232 1318468 Ark2n arkadia (RNF111) N-terminal like PKA signaling regulator 2N gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20221201 MGI PMID:35882232 1318468 Ark2n arkadia (RNF111) N-terminal like PKA signaling regulator 2N gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20221201 MGI PMID:35882232 1318468 Ark2n arkadia (RNF111) N-terminal like PKA signaling regulator 2N gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20221201 MGI PMID:35882232 1318468 Ark2n arkadia (RNF111) N-terminal like PKA signaling regulator 2N gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20221201 MGI PMID:35882232 1318468 Ark2n arkadia (RNF111) N-terminal like PKA signaling regulator 2N gene MP:0014145 increased white adipose tissue mass IAGP N RGD:5509061 20221201 MGI PMID:35882232 1318472 Wars2 tryptophanyl tRNA synthetase 2 (mitochondrial) gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20210826 MGI 1318472 Wars2 tryptophanyl tRNA synthetase 2 (mitochondrial) gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20160929 MGI PMID:27534441 1318472 Wars2 tryptophanyl tRNA synthetase 2 (mitochondrial) gene MP:0006325 impaired hearing IAGP N RGD:5509061 20160929 MGI PMID:27534441 1318472 Wars2 tryptophanyl tRNA synthetase 2 (mitochondrial) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318472 Wars2 tryptophanyl tRNA synthetase 2 (mitochondrial) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1318472 Wars2 tryptophanyl tRNA synthetase 2 (mitochondrial) gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1318472 Wars2 tryptophanyl tRNA synthetase 2 (mitochondrial) gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20160929 MGI PMID:27534441 1318474 Spdef SAM pointed domain containing ets transcription factor gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20801882 1318474 Spdef SAM pointed domain containing ets transcription factor gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:19549527 1318474 Spdef SAM pointed domain containing ets transcription factor gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:20801882 1318474 Spdef SAM pointed domain containing ets transcription factor gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:20801882 1318474 Spdef SAM pointed domain containing ets transcription factor gene MP:0002241 abnormal laryngeal mucosa goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19759516 1318474 Spdef SAM pointed domain containing ets transcription factor gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:20801882 1318474 Spdef SAM pointed domain containing ets transcription factor gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19549527 1318474 Spdef SAM pointed domain containing ets transcription factor gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19549527 1318474 Spdef SAM pointed domain containing ets transcription factor gene MP:0010790 abnormal stomach pyloric antrum morphology IAGP N RGD:5509061 20141003 MGI PMID:20801882 1318474 Spdef SAM pointed domain containing ets transcription factor gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:20801882 1318474 Spdef SAM pointed domain containing ets transcription factor gene MP:0010863 absent respiratory mucosa goblet cells IAGP N RGD:5509061 20141003 MGI PMID:19759516 1318474 Spdef SAM pointed domain containing ets transcription factor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20801882 1318474 Spdef SAM pointed domain containing ets transcription factor gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20150312 MGI PMID:19549527 1318476 Elovl2 ELOVL fatty acid elongase 2 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21106902 1318476 Elovl2 ELOVL fatty acid elongase 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20211104 MGI PMID:31943697 1318476 Elovl2 ELOVL fatty acid elongase 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:21106902 1318476 Elovl2 ELOVL fatty acid elongase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21106902 1318476 Elovl2 ELOVL fatty acid elongase 2 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20211104 MGI PMID:31943697 1318476 Elovl2 ELOVL fatty acid elongase 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20211104 MGI PMID:31943697 1318476 Elovl2 ELOVL fatty acid elongase 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21106902 1318476 Elovl2 ELOVL fatty acid elongase 2 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21106902 1318476 Elovl2 ELOVL fatty acid elongase 2 gene MP:0005283 increased unsaturated fatty acids level IAGP N RGD:5509061 20211104 MGI PMID:31943697 1318476 Elovl2 ELOVL fatty acid elongase 2 gene MP:0005285 decreased unsaturated fatty acids level IAGP N RGD:5509061 20211104 MGI PMID:31943697 1318476 Elovl2 ELOVL fatty acid elongase 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21106902 1318476 Elovl2 ELOVL fatty acid elongase 2 gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20211104 MGI PMID:31943697 1318476 Elovl2 ELOVL fatty acid elongase 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:21106902 1318478 Klk14 kallikrein related-peptidase 14 gene MP:0002959 increased urine microalbumin level IEA N RGD:5509061 20211021 MGI 1318478 Klk14 kallikrein related-peptidase 14 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1318478 Klk14 kallikrein related-peptidase 14 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20240523 MGI 1318481 Alkbh4 alkB homolog 4, lysine demethylase gene MP:0003707 increased cell nucleus count IAGP N RGD:5509061 20141003 MGI PMID:23673617 1318481 Alkbh4 alkB homolog 4, lysine demethylase gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23673617 1318481 Alkbh4 alkB homolog 4, lysine demethylase gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:23673617 1318481 Alkbh4 alkB homolog 4, lysine demethylase gene MP:0013289 abnormal mitotic cytokinesis IAGP N RGD:5509061 20190718 MGI PMID:23673617 1318481 Alkbh4 alkB homolog 4, lysine demethylase gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:23673617 1318483 Pop1 processing of precursor 1, ribonuclease P/MRP family, (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12393806 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:14567973 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:14567973 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:14738878 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12393806 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12393806 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14567973 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14738878 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12393806 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12393806 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:14738878 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12393806 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14567973 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12393806 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16642288 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16642288 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:16642288 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:16642288 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:14738878 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:14567973 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:14738878 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12393806 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:14567973 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:12393806 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:14738878 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:14567973 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:14738878 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:14567973 1318485 Slc19a2 solute carrier family 19 (thiamine transporter), member 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16642288 1318487 Mrgbp MRG/MORF4L binding protein gene MP:0001513 limb grasping IEA N RGD:5509061 20220811 MGI 1318487 Mrgbp MRG/MORF4L binding protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1318487 Mrgbp MRG/MORF4L binding protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1318490 Aldh7a1 aldehyde dehydrogenase family 7, member A1 gene MP:0002064 seizures IAGP N RGD:5509061 20210121 MGI PMID:32969477 1318490 Aldh7a1 aldehyde dehydrogenase family 7, member A1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1318490 Aldh7a1 aldehyde dehydrogenase family 7, member A1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20210121 MGI PMID:32969477 1318490 Aldh7a1 aldehyde dehydrogenase family 7, member A1 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20210121 MGI PMID:32969477 1318490 Aldh7a1 aldehyde dehydrogenase family 7, member A1 gene MP:0005400 abnormal vitamin level IAGP N RGD:5509061 20210121 MGI PMID:32969477 1318490 Aldh7a1 aldehyde dehydrogenase family 7, member A1 gene MP:0005665 increased circulating noradrenaline level IAGP N RGD:5509061 20210121 MGI PMID:32969477 1318490 Aldh7a1 aldehyde dehydrogenase family 7, member A1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210121 MGI PMID:32969477 1318490 Aldh7a1 aldehyde dehydrogenase family 7, member A1 gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20210121 MGI PMID:32969477 1318490 Aldh7a1 aldehyde dehydrogenase family 7, member A1 gene MP:0020237 increased proline level IAGP N RGD:5509061 20210121 MGI PMID:32969477 1318490 Aldh7a1 aldehyde dehydrogenase family 7, member A1 gene MP:0030647 increased ornithine level IAGP N RGD:5509061 20210121 MGI PMID:32969477 1318490 Aldh7a1 aldehyde dehydrogenase family 7, member A1 gene MP:0030659 decreased glycine level IAGP N RGD:5509061 20210121 MGI PMID:32969477 1318490 Aldh7a1 aldehyde dehydrogenase family 7, member A1 gene MP:0030691 increased serine level IAGP N RGD:5509061 20210121 MGI PMID:32969477 1318490 Aldh7a1 aldehyde dehydrogenase family 7, member A1 gene MP:0030697 increased phenylalanine level IAGP N RGD:5509061 20210121 MGI PMID:32969477 1318490 Aldh7a1 aldehyde dehydrogenase family 7, member A1 gene MP:0030722 decreased lysine level IAGP N RGD:5509061 20210121 MGI PMID:32969477 1318490 Aldh7a1 aldehyde dehydrogenase family 7, member A1 gene MP:0030747 increased leucine level IAGP N RGD:5509061 20210121 MGI PMID:32969477 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20230504 MGI PMID:37053259 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20230504 MGI PMID:37053259 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20230504 MGI PMID:37053259 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20230504 MGI PMID:37053259 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230504 MGI PMID:37053259 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20240523 MGI 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20240523 MGI 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20230504 MGI PMID:37053259 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20240523 MGI 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20230504 MGI PMID:37053259 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20230504 MGI PMID:37053259 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20230504 MGI PMID:37053259 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20230504 MGI PMID:37053259 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0005352 small cranium IAGP N RGD:5509061 20230504 MGI PMID:37053259 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20230504 MGI PMID:37053259 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20230504 MGI PMID:37053259 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0009908 protruding tongue IEA N RGD:5509061 20240523 MGI 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20230504 MGI PMID:37053259 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1318492 Slc35a3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 gene MP:0011475 abnormal glycosaminoglycan level IAGP N RGD:5509061 20230504 MGI PMID:37053259 1318493 Szt2 SZT2 subunit of KICSTOR complex gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:19624305 1318493 Szt2 SZT2 subunit of KICSTOR complex gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1318493 Szt2 SZT2 subunit of KICSTOR complex gene MP:0001499 abnormal kindling response IAGP N RGD:5509061 20141003 MGI PMID:19624305 1318493 Szt2 SZT2 subunit of KICSTOR complex gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 1318493 Szt2 SZT2 subunit of KICSTOR complex gene MP:0001785 edema IEA N RGD:5509061 20230601 MGI 1318493 Szt2 SZT2 subunit of KICSTOR complex gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1318493 Szt2 SZT2 subunit of KICSTOR complex gene MP:0002193 minimal clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19624305 1318493 Szt2 SZT2 subunit of KICSTOR complex gene MP:0002194 maximal tonic hindlimb extension seizures IAGP N RGD:5509061 20141003 MGI PMID:19624305 1318493 Szt2 SZT2 subunit of KICSTOR complex gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:19624305 1318493 Szt2 SZT2 subunit of KICSTOR complex gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19624305 1318493 Szt2 SZT2 subunit of KICSTOR complex gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19624305 1318493 Szt2 SZT2 subunit of KICSTOR complex gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19624305 1318493 Szt2 SZT2 subunit of KICSTOR complex gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19624305 1318495 Zfp287 zinc finger protein 287 gene MP:0001406 abnormal gait IEA N RGD:5509061 20170105 MGI 1318497 Tagap1 T cell activation GTPase activating protein 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1318497 Tagap1 T cell activation GTPase activating protein 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1318497 Tagap1 T cell activation GTPase activating protein 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20220519 MGI 1318497 Tagap1 T cell activation GTPase activating protein 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1318497 Tagap1 T cell activation GTPase activating protein 1 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20210128 MGI 1318497 Tagap1 T cell activation GTPase activating protein 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20220519 MGI 1318497 Tagap1 T cell activation GTPase activating protein 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1318497 Tagap1 T cell activation GTPase activating protein 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1318500 Zfp334 zinc finger protein 334 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1318500 Zfp334 zinc finger protein 334 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1318500 Zfp334 zinc finger protein 334 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20181227 MGI 1318500 Zfp334 zinc finger protein 334 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1318504 Pdzd8 PDZ domain containing 8 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0001258 decreased body length IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1318504 Pdzd8 PDZ domain containing 8 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1318504 Pdzd8 PDZ domain containing 8 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1318504 Pdzd8 PDZ domain containing 8 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20210128 MGI 1318504 Pdzd8 PDZ domain containing 8 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1318504 Pdzd8 PDZ domain containing 8 gene MP:0002764 short tibia IEA N RGD:5509061 20230601 MGI 1318504 Pdzd8 PDZ domain containing 8 gene MP:0002892 decreased superior colliculus size IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 1318504 Pdzd8 PDZ domain containing 8 gene MP:0004081 abnormal globus pallidus morphology IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20210128 MGI 1318504 Pdzd8 PDZ domain containing 8 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20220811 MGI 1318504 Pdzd8 PDZ domain containing 8 gene MP:0008282 enlarged hippocampus IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1318504 Pdzd8 PDZ domain containing 8 gene MP:0008914 enlarged cerebellum IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0009849 increased vertical stereotypic behavior IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0010058 enlarged olfactory bulb IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1318504 Pdzd8 PDZ domain containing 8 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20210128 MGI 1318504 Pdzd8 PDZ domain containing 8 gene MP:0012489 abnormal retrosplenial region morphology IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318504 Pdzd8 PDZ domain containing 8 gene MP:0020527 small thalamus IAGP N RGD:5509061 20220825 MGI PMID:35227461 1318507 Neu4 sialidase 4 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:18270209 1318507 Neu4 sialidase 4 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:18270209 1318507 Neu4 sialidase 4 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18270209 1318507 Neu4 sialidase 4 gene MP:0005283 increased unsaturated fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18270209 1318507 Neu4 sialidase 4 gene MP:0031632 increased lung cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:18270209 1318508 Gtf2a1l general transcription factor IIA, 1-like gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20240523 MGI 1318508 Gtf2a1l general transcription factor IIA, 1-like gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20240523 MGI 1318508 Gtf2a1l general transcription factor IIA, 1-like gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20240523 MGI 1318514 Crybg1 crystallin beta-gamma domain containing 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20221215 MGI 1318514 Crybg1 crystallin beta-gamma domain containing 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1318514 Crybg1 crystallin beta-gamma domain containing 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1318514 Crybg1 crystallin beta-gamma domain containing 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20160421 MGI 1318514 Crybg1 crystallin beta-gamma domain containing 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1318514 Crybg1 crystallin beta-gamma domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1318514 Crybg1 crystallin beta-gamma domain containing 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:22069191 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:22069191 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:22069191 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17535917 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:17535917 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17535917 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16510869 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22069191 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:22069191 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17535917 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:22069191 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16510869 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17535917 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17535917 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:16510869 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:16510869 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:22069191 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:22069191 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16510869 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17535917 1318518 Maml1 mastermind like transcriptional coactivator 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22069191 1318523 Amn amnionless gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20150219 MGI 1318523 Amn amnionless gene MP:0000484 abnormal pulmonary artery morphology IEA N RGD:5509061 20150219 MGI 1318523 Amn amnionless gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:8660894 1318523 Amn amnionless gene MP:0001297 microphthalmia IEA N RGD:5509061 20150219 MGI 1318523 Amn amnionless gene MP:0001625 cardiac hypertrophy IEA N RGD:5509061 20150219 MGI 1318523 Amn amnionless gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:8660894 1318523 Amn amnionless gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:9851841 1318523 Amn amnionless gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:8660894 1318523 Amn amnionless gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9851841 1318523 Amn amnionless gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11279523 1318523 Amn amnionless gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:8660894 1318523 Amn amnionless gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9825865 1318523 Amn amnionless gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:9851841 1318523 Amn amnionless gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:9825865 1318523 Amn amnionless gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:8660894 1318523 Amn amnionless gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:9851841 1318523 Amn amnionless gene MP:0004158 right aortic arch IEA N RGD:5509061 20150219 MGI 1318523 Amn amnionless gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:8660894 1318523 Amn amnionless gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:9851841 1318523 Amn amnionless gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:8660894 1318523 Amn amnionless gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:9851841 1318523 Amn amnionless gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:8660894 1318523 Amn amnionless gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:9851841 1318523 Amn amnionless gene MP:0010466 vascular ring IEA N RGD:5509061 20150219 MGI 1318523 Amn amnionless gene MP:0010488 abnormal left subclavian artery morphology IEA N RGD:5509061 20150219 MGI 1318523 Amn amnionless gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8660894 1318523 Amn amnionless gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11279523 1318523 Amn amnionless gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9851841 1318523 Amn amnionless gene MP:0011666 double outlet right ventricle, ventricular defect committed to aorta IEA N RGD:5509061 20150219 MGI 1318523 Amn amnionless gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:9825865 1318526 Ccdc90b coiled-coil domain containing 90B gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1318526 Ccdc90b coiled-coil domain containing 90B gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1318529 Dkk4 dickkopf WNT signaling pathway inhibitor 4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1318529 Dkk4 dickkopf WNT signaling pathway inhibitor 4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1318529 Dkk4 dickkopf WNT signaling pathway inhibitor 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 1318529 Dkk4 dickkopf WNT signaling pathway inhibitor 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1318532 Txnl4a thioredoxin-like 4A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1318537 Slfn2 schlafen 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20190759 1318537 Slfn2 schlafen 2 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20190759 1318537 Slfn2 schlafen 2 gene MP:0001805 decreased IgG level IEA N RGD:5509061 20160915 MGI 1318537 Slfn2 schlafen 2 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:20190759 1318537 Slfn2 schlafen 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20190759 1318537 Slfn2 schlafen 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20190759 1318537 Slfn2 schlafen 2 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20190759 1318537 Slfn2 schlafen 2 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20190759 1318537 Slfn2 schlafen 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20190759 1318537 Slfn2 schlafen 2 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20190759 1318537 Slfn2 schlafen 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20190759 1318537 Slfn2 schlafen 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20190759 1318537 Slfn2 schlafen 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20190759 1318537 Slfn2 schlafen 2 gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20160915 MGI 1318537 Slfn2 schlafen 2 gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20160915 MGI 1318537 Slfn2 schlafen 2 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:20190759 1318537 Slfn2 schlafen 2 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:20190759 1318540 Abtb3 ankyrin repeat and BTB domain containing 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20230921 MGI PMID:37261953 1318540 Abtb3 ankyrin repeat and BTB domain containing 3 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20230921 MGI PMID:37261953 1318540 Abtb3 ankyrin repeat and BTB domain containing 3 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20230921 MGI PMID:37261953 1318540 Abtb3 ankyrin repeat and BTB domain containing 3 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20230921 MGI PMID:37261953 1318540 Abtb3 ankyrin repeat and BTB domain containing 3 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20230921 MGI PMID:37261953 1318540 Abtb3 ankyrin repeat and BTB domain containing 3 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:37261953 1318540 Abtb3 ankyrin repeat and BTB domain containing 3 gene MP:0020422 decreased freezing behavior IAGP N RGD:5509061 20230921 MGI PMID:37261953 1318540 Abtb3 ankyrin repeat and BTB domain containing 3 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20230921 MGI PMID:37261953 1318540 Abtb3 ankyrin repeat and BTB domain containing 3 gene MP:0021010 impaired synaptic physiology IAGP N RGD:5509061 20230921 MGI PMID:37261953 1318542 Sntb2 syntrophin, basic 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:15548643 1318542 Sntb2 syntrophin, basic 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15548643 1318542 Sntb2 syntrophin, basic 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15548643 1318542 Sntb2 syntrophin, basic 2 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:15548643 1318545 Sema5a sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15743826 1318545 Sema5a sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1318545 Sema5a sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:15743826 1318545 Sema5a sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318545 Sema5a sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318545 Sema5a sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318545 Sema5a sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318545 Sema5a sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318545 Sema5a sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318545 Sema5a sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318545 Sema5a sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318545 Sema5a sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318545 Sema5a sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318545 Sema5a sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318545 Sema5a sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15743826 1318549 Stk11 serine/threonine kinase 11 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0000088 short mandible IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21606593 1318549 Stk11 serine/threonine kinase 11 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21124450 1318549 Stk11 serine/threonine kinase 11 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21124450 1318549 Stk11 serine/threonine kinase 11 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23266956 1318549 Stk11 serine/threonine kinase 11 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18172296 1318549 Stk11 serine/threonine kinase 11 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:18172296 1318549 Stk11 serine/threonine kinase 11 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:18172296 1318549 Stk11 serine/threonine kinase 11 gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:18172296 1318549 Stk11 serine/threonine kinase 11 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0000445 short snout IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:16357136 1318549 Stk11 serine/threonine kinase 11 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:20142330 1318549 Stk11 serine/threonine kinase 11 gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:20142330 1318549 Stk11 serine/threonine kinase 11 gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20160915 MGI PMID:21283818 1318549 Stk11 serine/threonine kinase 11 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:16357136 1318549 Stk11 serine/threonine kinase 11 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16278673 1318549 Stk11 serine/threonine kinase 11 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:23451056 1318549 Stk11 serine/threonine kinase 11 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16357136 1318549 Stk11 serine/threonine kinase 11 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23790753 1318549 Stk11 serine/threonine kinase 11 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 1318549 Stk11 serine/threonine kinase 11 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:22791749 1318549 Stk11 serine/threonine kinase 11 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22791749 1318549 Stk11 serine/threonine kinase 11 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:23266956 1318549 Stk11 serine/threonine kinase 11 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:18172296 1318549 Stk11 serine/threonine kinase 11 gene MP:0001255 decreased body height IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18172296 1318549 Stk11 serine/threonine kinase 11 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:12218179 1318549 Stk11 serine/threonine kinase 11 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:16357136 1318549 Stk11 serine/threonine kinase 11 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:20142330 1318549 Stk11 serine/threonine kinase 11 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20150910 MGI PMID:17676035 1318549 Stk11 serine/threonine kinase 11 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160331 MGI PMID:25252692 1318549 Stk11 serine/threonine kinase 11 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:18172296 1318549 Stk11 serine/threonine kinase 11 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:12226664 1318549 Stk11 serine/threonine kinase 11 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:12226664 1318549 Stk11 serine/threonine kinase 11 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12060709 1318549 Stk11 serine/threonine kinase 11 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12060709 1318549 Stk11 serine/threonine kinase 11 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:12226664 1318549 Stk11 serine/threonine kinase 11 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21124450 1318549 Stk11 serine/threonine kinase 11 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:18227155 1318549 Stk11 serine/threonine kinase 11 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15889149 1318549 Stk11 serine/threonine kinase 11 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11956081 1318549 Stk11 serine/threonine kinase 11 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12226664 1318549 Stk11 serine/threonine kinase 11 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16278673 1318549 Stk11 serine/threonine kinase 11 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18172296 1318549 Stk11 serine/threonine kinase 11 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20150910 MGI PMID:17676035 1318549 Stk11 serine/threonine kinase 11 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16357136 1318549 Stk11 serine/threonine kinase 11 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15480979 1318549 Stk11 serine/threonine kinase 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11956081 1318549 Stk11 serine/threonine kinase 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12218179 1318549 Stk11 serine/threonine kinase 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16278673 1318549 Stk11 serine/threonine kinase 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16357136 1318549 Stk11 serine/threonine kinase 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18172296 1318549 Stk11 serine/threonine kinase 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18311138 1318549 Stk11 serine/threonine kinase 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20142330 1318549 Stk11 serine/threonine kinase 11 gene MP:0002083 premature death IAGP N RGD:5509061 20150910 MGI PMID:17676035 1318549 Stk11 serine/threonine kinase 11 gene MP:0002083 premature death IAGP N RGD:5509061 20160915 MGI PMID:21283818 1318549 Stk11 serine/threonine kinase 11 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:24295069 1318549 Stk11 serine/threonine kinase 11 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24295069 1318549 Stk11 serine/threonine kinase 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12226664 1318549 Stk11 serine/threonine kinase 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24295069 1318549 Stk11 serine/threonine kinase 11 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 1318549 Stk11 serine/threonine kinase 11 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21124450 1318549 Stk11 serine/threonine kinase 11 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12060709 1318549 Stk11 serine/threonine kinase 11 gene MP:0002639 micrognathia IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 1318549 Stk11 serine/threonine kinase 11 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21124450 1318549 Stk11 serine/threonine kinase 11 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:12218179 1318549 Stk11 serine/threonine kinase 11 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:12226664 1318549 Stk11 serine/threonine kinase 11 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21124450 1318549 Stk11 serine/threonine kinase 11 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:12226664 1318549 Stk11 serine/threonine kinase 11 gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:16357136 1318549 Stk11 serine/threonine kinase 11 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:12218179 1318549 Stk11 serine/threonine kinase 11 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:12226664 1318549 Stk11 serine/threonine kinase 11 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:18311138 1318549 Stk11 serine/threonine kinase 11 gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:11956081 1318549 Stk11 serine/threonine kinase 11 gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:12060709 1318549 Stk11 serine/threonine kinase 11 gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:12218179 1318549 Stk11 serine/threonine kinase 11 gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:12226664 1318549 Stk11 serine/threonine kinase 11 gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:15480979 1318549 Stk11 serine/threonine kinase 11 gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:16357136 1318549 Stk11 serine/threonine kinase 11 gene MP:0003299 gastric polyps IAGP N RGD:5509061 20160915 MGI PMID:21283818 1318549 Stk11 serine/threonine kinase 11 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:20142330 1318549 Stk11 serine/threonine kinase 11 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12218179 1318549 Stk11 serine/threonine kinase 11 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11956081 1318549 Stk11 serine/threonine kinase 11 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12218179 1318549 Stk11 serine/threonine kinase 11 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16278673 1318549 Stk11 serine/threonine kinase 11 gene MP:0003334 pancreas fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18227155 1318549 Stk11 serine/threonine kinase 11 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:23266956 1318549 Stk11 serine/threonine kinase 11 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:18227155 1318549 Stk11 serine/threonine kinase 11 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:21266325 1318549 Stk11 serine/threonine kinase 11 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:21606593 1318549 Stk11 serine/threonine kinase 11 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20210603 MGI PMID:32414840 1318549 Stk11 serine/threonine kinase 11 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16357136 1318549 Stk11 serine/threonine kinase 11 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:18172296 1318549 Stk11 serine/threonine kinase 11 gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:16357136 1318549 Stk11 serine/threonine kinase 11 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12060709 1318549 Stk11 serine/threonine kinase 11 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:21124450 1318549 Stk11 serine/threonine kinase 11 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18172296 1318549 Stk11 serine/threonine kinase 11 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:18227155 1318549 Stk11 serine/threonine kinase 11 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:18172296 1318549 Stk11 serine/threonine kinase 11 gene MP:0004540 small maxilla IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21124450 1318549 Stk11 serine/threonine kinase 11 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21124450 1318549 Stk11 serine/threonine kinase 11 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20210603 MGI PMID:32414840 1318549 Stk11 serine/threonine kinase 11 gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22791749 1318549 Stk11 serine/threonine kinase 11 gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12218179 1318549 Stk11 serine/threonine kinase 11 gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18245476 1318549 Stk11 serine/threonine kinase 11 gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20142330 1318549 Stk11 serine/threonine kinase 11 gene MP:0004870 small premaxilla IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:22791749 1318549 Stk11 serine/threonine kinase 11 gene MP:0004902 abnormal uterus size IAGP N RGD:5509061 20141003 MGI PMID:20142330 1318549 Stk11 serine/threonine kinase 11 gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:20142330 1318549 Stk11 serine/threonine kinase 11 gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:20142330 1318549 Stk11 serine/threonine kinase 11 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18840652 1318549 Stk11 serine/threonine kinase 11 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:21124450 1318549 Stk11 serine/threonine kinase 11 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:18227155 1318549 Stk11 serine/threonine kinase 11 gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:18227155 1318549 Stk11 serine/threonine kinase 11 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18227155 1318549 Stk11 serine/threonine kinase 11 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21266325 1318549 Stk11 serine/threonine kinase 11 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21266325 1318549 Stk11 serine/threonine kinase 11 gene MP:0005352 small cranium IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20210603 MGI PMID:32414840 1318549 Stk11 serine/threonine kinase 11 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:23597566 1318549 Stk11 serine/threonine kinase 11 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21266325 1318549 Stk11 serine/threonine kinase 11 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18227155 1318549 Stk11 serine/threonine kinase 11 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21606593 1318549 Stk11 serine/threonine kinase 11 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12226664 1318549 Stk11 serine/threonine kinase 11 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24295069 1318549 Stk11 serine/threonine kinase 11 gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20141003 MGI PMID:21124450 1318549 Stk11 serine/threonine kinase 11 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23790753 1318549 Stk11 serine/threonine kinase 11 gene MP:0006342 absent first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16278673 1318549 Stk11 serine/threonine kinase 11 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:12218179 1318549 Stk11 serine/threonine kinase 11 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:15480979 1318549 Stk11 serine/threonine kinase 11 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:18245476 1318549 Stk11 serine/threonine kinase 11 gene MP:0008012 duodenum polyps IAGP N RGD:5509061 20150702 MGI PMID:12218179 1318549 Stk11 serine/threonine kinase 11 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20150910 MGI PMID:17676035 1318549 Stk11 serine/threonine kinase 11 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16278673 1318549 Stk11 serine/threonine kinase 11 gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:20142330 1318549 Stk11 serine/threonine kinase 11 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:23241891 1318549 Stk11 serine/threonine kinase 11 gene MP:0008717 increased lung squamous cell carcinoma incidence IAGP N RGD:5509061 20150910 MGI PMID:17676035 1318549 Stk11 serine/threonine kinase 11 gene MP:0008718 increased lung large cell carcinoma incidence IAGP N RGD:5509061 20150910 MGI PMID:17676035 1318549 Stk11 serine/threonine kinase 11 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:18227155 1318549 Stk11 serine/threonine kinase 11 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18227155 1318549 Stk11 serine/threonine kinase 11 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:18227155 1318549 Stk11 serine/threonine kinase 11 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:18227155 1318549 Stk11 serine/threonine kinase 11 gene MP:0009181 decreased pancreatic delta cell number IAGP N RGD:5509061 20141003 MGI PMID:18227155 1318549 Stk11 serine/threonine kinase 11 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21124450 1318549 Stk11 serine/threonine kinase 11 gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20160915 MGI PMID:21283818 1318549 Stk11 serine/threonine kinase 11 gene MP:0009552 urinary bladder obstruction IAGP N RGD:5509061 20141003 MGI PMID:20142330 1318549 Stk11 serine/threonine kinase 11 gene MP:0009552 urinary bladder obstruction IAGP N RGD:5509061 20160915 MGI PMID:21283818 1318549 Stk11 serine/threonine kinase 11 gene MP:0009656 delayed chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:21124450 1318549 Stk11 serine/threonine kinase 11 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18311138 1318549 Stk11 serine/threonine kinase 11 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23790753 1318549 Stk11 serine/threonine kinase 11 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23451056 1318549 Stk11 serine/threonine kinase 11 gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11956081 1318549 Stk11 serine/threonine kinase 11 gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12226664 1318549 Stk11 serine/threonine kinase 11 gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16278673 1318549 Stk11 serine/threonine kinase 11 gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16357136 1318549 Stk11 serine/threonine kinase 11 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:23451056 1318549 Stk11 serine/threonine kinase 11 gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20160331 MGI PMID:25252692 1318549 Stk11 serine/threonine kinase 11 gene MP:0010352 gastrointestinal tract polyps IAGP N RGD:5509061 20141003 MGI PMID:12226664 1318549 Stk11 serine/threonine kinase 11 gene MP:0010352 gastrointestinal tract polyps IAGP N RGD:5509061 20141003 MGI PMID:18311138 1318549 Stk11 serine/threonine kinase 11 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12060709 1318549 Stk11 serine/threonine kinase 11 gene MP:0010906 abnormal lung bud morphology IAGP N RGD:5509061 20141003 MGI PMID:23266956 1318549 Stk11 serine/threonine kinase 11 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:23266956 1318549 Stk11 serine/threonine kinase 11 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15889149 1318549 Stk11 serine/threonine kinase 11 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11956081 1318549 Stk11 serine/threonine kinase 11 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12226664 1318549 Stk11 serine/threonine kinase 11 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16357136 1318549 Stk11 serine/threonine kinase 11 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12060709 1318549 Stk11 serine/threonine kinase 11 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23266956 1318549 Stk11 serine/threonine kinase 11 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:12060709 1318549 Stk11 serine/threonine kinase 11 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 1318549 Stk11 serine/threonine kinase 11 gene MP:0011766 abnormal urinary bladder mucosa morphology IAGP N RGD:5509061 20160915 MGI PMID:21283818 1318549 Stk11 serine/threonine kinase 11 gene MP:0011874 enlarged urinary bladder IAGP N RGD:5509061 20160915 MGI PMID:21283818 1318549 Stk11 serine/threonine kinase 11 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:21266325 1318549 Stk11 serine/threonine kinase 11 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16357136 1318549 Stk11 serine/threonine kinase 11 gene MP:0013220 increased pancreas apoptosis IAGP N RGD:5509061 20160428 MGI PMID:18227155 1318549 Stk11 serine/threonine kinase 11 gene MP:0013267 first pharyngeal arch hypoplasia IAGP N RGD:5509061 20171109 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0013328 visceromegaly IAGP N RGD:5509061 20141204 MGI PMID:16357136 1318549 Stk11 serine/threonine kinase 11 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:23790753 1318549 Stk11 serine/threonine kinase 11 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0030022 decreased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:15889149 1318549 Stk11 serine/threonine kinase 11 gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0030266 small vomer bone IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0030383 small presphenoid bone IAGP N RGD:5509061 20221013 MGI PMID:27527806 1318549 Stk11 serine/threonine kinase 11 gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:11509733 1318549 Stk11 serine/threonine kinase 11 gene MP:0031407 increased Sertoli cell proliferation IAGP N RGD:5509061 20220630 MGI PMID:22791749 1318554 Lamc1 laminin, gamma 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:14638863 1318554 Lamc1 laminin, gamma 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:14638863 1318554 Lamc1 laminin, gamma 1 gene MP:0000756 forelimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:14638863 1318554 Lamc1 laminin, gamma 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:12122064 1318554 Lamc1 laminin, gamma 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12122064 1318554 Lamc1 laminin, gamma 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16873583 1318554 Lamc1 laminin, gamma 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:17942732 1318554 Lamc1 laminin, gamma 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12122064 1318554 Lamc1 laminin, gamma 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:14638863 1318554 Lamc1 laminin, gamma 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:22767514 1318554 Lamc1 laminin, gamma 1 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14638863 1318554 Lamc1 laminin, gamma 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12122064 1318554 Lamc1 laminin, gamma 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:12122064 1318554 Lamc1 laminin, gamma 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22767514 1318554 Lamc1 laminin, gamma 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12122064 1318554 Lamc1 laminin, gamma 1 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14638863 1318554 Lamc1 laminin, gamma 1 gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:14638863 1318554 Lamc1 laminin, gamma 1 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:14638863 1318554 Lamc1 laminin, gamma 1 gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0003558 absent uterus IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12122064 1318554 Lamc1 laminin, gamma 1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16873583 1318554 Lamc1 laminin, gamma 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:12122064 1318554 Lamc1 laminin, gamma 1 gene MP:0003826 abnormal Mullerian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:14638863 1318554 Lamc1 laminin, gamma 1 gene MP:0003994 abnormal dorsal spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:14638863 1318554 Lamc1 laminin, gamma 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0004220 abnormal peripheral nervous system regeneration IAGP N RGD:5509061 20141003 MGI PMID:14638863 1318554 Lamc1 laminin, gamma 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12122064 1318554 Lamc1 laminin, gamma 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16873583 1318554 Lamc1 laminin, gamma 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:22767514 1318554 Lamc1 laminin, gamma 1 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:22767514 1318554 Lamc1 laminin, gamma 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:14638863 1318554 Lamc1 laminin, gamma 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0005623 abnormal meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:12122064 1318554 Lamc1 laminin, gamma 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16873583 1318554 Lamc1 laminin, gamma 1 gene MP:0008030 abnormal Cajal-Retzius cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12122064 1318554 Lamc1 laminin, gamma 1 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16873583 1318554 Lamc1 laminin, gamma 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:22767514 1318554 Lamc1 laminin, gamma 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:22767514 1318554 Lamc1 laminin, gamma 1 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:22767514 1318554 Lamc1 laminin, gamma 1 gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:22767514 1318554 Lamc1 laminin, gamma 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:12122064 1318554 Lamc1 laminin, gamma 1 gene MP:0010225 abnormal quadriceps morphology IAGP N RGD:5509061 20141003 MGI PMID:22767514 1318554 Lamc1 laminin, gamma 1 gene MP:0010451 kidney microaneurysm IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0010742 increased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:22767514 1318554 Lamc1 laminin, gamma 1 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20191114 MGI PMID:30456378 1318554 Lamc1 laminin, gamma 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11431694 1318554 Lamc1 laminin, gamma 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9885251 1318554 Lamc1 laminin, gamma 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9885251 1318554 Lamc1 laminin, gamma 1 gene MP:0011206 absent visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:9885251 1318554 Lamc1 laminin, gamma 1 gene MP:0011366 absent metanephros IAGP N RGD:5509061 20141003 MGI PMID:12015298 1318554 Lamc1 laminin, gamma 1 gene MP:0020452 abnormal axon radial sorting IAGP N RGD:5509061 20170914 MGI PMID:14638863 1318556 Thoc1 THO complex 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240523 MGI 1318556 Thoc1 THO complex 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20240523 MGI 1318556 Thoc1 THO complex 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1318556 Thoc1 THO complex 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 1318556 Thoc1 THO complex 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 1318556 Thoc1 THO complex 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17211872 1318556 Thoc1 THO complex 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17211872 1318556 Thoc1 THO complex 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17211872 1318556 Thoc1 THO complex 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17211872 1318556 Thoc1 THO complex 1 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 1318556 Thoc1 THO complex 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20240523 MGI 1318556 Thoc1 THO complex 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1318556 Thoc1 THO complex 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:16705185 1318556 Thoc1 THO complex 1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20240523 MGI 1318556 Thoc1 THO complex 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230119 MGI 1318556 Thoc1 THO complex 1 gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:16705185 1318556 Thoc1 THO complex 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1318556 Thoc1 THO complex 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230119 MGI 1318556 Thoc1 THO complex 1 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16705185 1318556 Thoc1 THO complex 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17211872 1318556 Thoc1 THO complex 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17211872 1318556 Thoc1 THO complex 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1318556 Thoc1 THO complex 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20240523 MGI 1318556 Thoc1 THO complex 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20240523 MGI 1318556 Thoc1 THO complex 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16705185 1318558 Pla2g4b phospholipase A2, group IVB (cytosolic) gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1318558 Pla2g4b phospholipase A2, group IVB (cytosolic) gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1318558 Pla2g4b phospholipase A2, group IVB (cytosolic) gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1318558 Pla2g4b phospholipase A2, group IVB (cytosolic) gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 1318558 Pla2g4b phospholipase A2, group IVB (cytosolic) gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1318564 Arhgap45 Rho GTPase activating protein 45 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20211209 MGI PMID:33719206 1318564 Arhgap45 Rho GTPase activating protein 45 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20211209 MGI PMID:33719206 1318564 Arhgap45 Rho GTPase activating protein 45 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20211209 MGI PMID:33719206 1318564 Arhgap45 Rho GTPase activating protein 45 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20211209 MGI PMID:33719206 1318564 Arhgap45 Rho GTPase activating protein 45 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20211209 MGI PMID:33719206 1318564 Arhgap45 Rho GTPase activating protein 45 gene MP:0008185 decreased naive B cell number IAGP N RGD:5509061 20211209 MGI PMID:33719206 1318564 Arhgap45 Rho GTPase activating protein 45 gene MP:0010130 decreased DN1 thymic pro-T cell number IAGP N RGD:5509061 20211209 MGI PMID:33719206 1318564 Arhgap45 Rho GTPase activating protein 45 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IAGP N RGD:5509061 20211209 MGI PMID:33719206 1318564 Arhgap45 Rho GTPase activating protein 45 gene MP:0031207 decreased lymphocyte chemotaxis IAGP N RGD:5509061 20211209 MGI PMID:33719206 1318568 Cdk2ap1 cyclin dependent kinase 2 associated protein 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:19229340 1318568 Cdk2ap1 cyclin dependent kinase 2 associated protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19229340 1318568 Cdk2ap1 cyclin dependent kinase 2 associated protein 1 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19229340 1318568 Cdk2ap1 cyclin dependent kinase 2 associated protein 1 gene MP:0030046 round forehead IAGP N RGD:5509061 20170921 MGI PMID:19229340 1318571 Proz protein Z, vitamin K-dependent plasma glycoprotein gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10829076 1318571 Proz protein Z, vitamin K-dependent plasma glycoprotein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10829076 1318571 Proz protein Z, vitamin K-dependent plasma glycoprotein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10829076 1318571 Proz protein Z, vitamin K-dependent plasma glycoprotein gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:10829076 1318571 Proz protein Z, vitamin K-dependent plasma glycoprotein gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18344422 1318571 Proz protein Z, vitamin K-dependent plasma glycoprotein gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:18344422 1318573 Fbln1 fibulin 1 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:19922873 1318573 Fbln1 fibulin 1 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:19922873 1318573 Fbln1 fibulin 1 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0003499 thyroid gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0004568 fusion of glossopharyngeal and vagus nerve IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0006203 eye hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0008816 petechiae IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0008816 petechiae IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0010405 ostium secundum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0010502 ventricle myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0011359 decreased glomerular capillary number IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0011509 dilated glomerular capillary IAGP N RGD:5509061 20141003 MGI PMID:11564885 1318573 Fbln1 fibulin 1 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:18538758 1318573 Fbln1 fibulin 1 gene MP:0030867 small thyroid cartilage IAGP N RGD:5509061 20181101 MGI PMID:18538758 1318575 Lingo1 leucine rich repeat and Ig domain containing 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15895088 1318577 Foxp1 forkhead box P1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15342473 1318577 Foxp1 forkhead box P1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:20713518 1318577 Foxp1 forkhead box P1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:20713518 1318577 Foxp1 forkhead box P1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15342473 1318577 Foxp1 forkhead box P1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:20713518 1318577 Foxp1 forkhead box P1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17428829 1318577 Foxp1 forkhead box P1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1318577 Foxp1 forkhead box P1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:15342473 1318577 Foxp1 forkhead box P1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17428829 1318577 Foxp1 forkhead box P1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16819554 1318577 Foxp1 forkhead box P1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:19965654 1318577 Foxp1 forkhead box P1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15342473 1318577 Foxp1 forkhead box P1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22675208 1318577 Foxp1 forkhead box P1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:22675208 1318577 Foxp1 forkhead box P1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16819554 1318577 Foxp1 forkhead box P1 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:15342473 1318577 Foxp1 forkhead box P1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:15342473 1318577 Foxp1 forkhead box P1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16819554 1318577 Foxp1 forkhead box P1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15342473 1318577 Foxp1 forkhead box P1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:18347093 1318577 Foxp1 forkhead box P1 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:20713518 1318577 Foxp1 forkhead box P1 gene MP:0003115 abnormal respiratory system development IAGP N RGD:5509061 20141003 MGI PMID:22675208 1318577 Foxp1 forkhead box P1 gene MP:0003159 abnormal esophageal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17428829 1318577 Foxp1 forkhead box P1 gene MP:0003160 abnormal esophagus development IAGP N RGD:5509061 20141003 MGI PMID:17428829 1318577 Foxp1 forkhead box P1 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20713518 1318577 Foxp1 forkhead box P1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:17428829 1318577 Foxp1 forkhead box P1 gene MP:0003808 increased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:15342473 1318577 Foxp1 forkhead box P1 gene MP:0003808 increased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:20713518 1318577 Foxp1 forkhead box P1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1318577 Foxp1 forkhead box P1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:20713518 1318577 Foxp1 forkhead box P1 gene MP:0004548 dilated esophagus IAGP N RGD:5509061 20141003 MGI PMID:17428829 1318577 Foxp1 forkhead box P1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22675208 1318577 Foxp1 forkhead box P1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15342473 1318577 Foxp1 forkhead box P1 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:17428829 1318577 Foxp1 forkhead box P1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:20713518 1318577 Foxp1 forkhead box P1 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19965654 1318577 Foxp1 forkhead box P1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19965654 1318577 Foxp1 forkhead box P1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19965654 1318577 Foxp1 forkhead box P1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16819554 1318577 Foxp1 forkhead box P1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15342473 1318577 Foxp1 forkhead box P1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18347093 1318577 Foxp1 forkhead box P1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20713518 1318577 Foxp1 forkhead box P1 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:15342473 1318577 Foxp1 forkhead box P1 gene MP:0010588 conotruncal ridge hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15342473 1318577 Foxp1 forkhead box P1 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:20713518 1318577 Foxp1 forkhead box P1 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:17428829 1318577 Foxp1 forkhead box P1 gene MP:0010949 decreased club cell number IAGP N RGD:5509061 20141003 MGI PMID:22675208 1318577 Foxp1 forkhead box P1 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17428829 1318577 Foxp1 forkhead box P1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20713518 1318577 Foxp1 forkhead box P1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22675208 1318577 Foxp1 forkhead box P1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17428829 1318577 Foxp1 forkhead box P1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17428829 1318577 Foxp1 forkhead box P1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16819554 1318577 Foxp1 forkhead box P1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20713518 1318577 Foxp1 forkhead box P1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318577 Foxp1 forkhead box P1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18347093 1318577 Foxp1 forkhead box P1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15342473 1318577 Foxp1 forkhead box P1 gene MP:0011148 decreased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:17428829 1318577 Foxp1 forkhead box P1 gene MP:0011394 increased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20713518 1318579 Fkbp8 FK506 binding protein 8 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0000576 clubfoot IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:18003640 1318579 Fkbp8 FK506 binding protein 8 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:15105374 1318579 Fkbp8 FK506 binding protein 8 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:18003640 1318579 Fkbp8 FK506 binding protein 8 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0000962 disorganized dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:18003640 1318579 Fkbp8 FK506 binding protein 8 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:15105374 1318579 Fkbp8 FK506 binding protein 8 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:15105374 1318579 Fkbp8 FK506 binding protein 8 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15105374 1318579 Fkbp8 FK506 binding protein 8 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:15105374 1318579 Fkbp8 FK506 binding protein 8 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15105374 1318579 Fkbp8 FK506 binding protein 8 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:18003640 1318579 Fkbp8 FK506 binding protein 8 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:15105374 1318579 Fkbp8 FK506 binding protein 8 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15105374 1318579 Fkbp8 FK506 binding protein 8 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18003640 1318579 Fkbp8 FK506 binding protein 8 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0002809 increased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:18003640 1318579 Fkbp8 FK506 binding protein 8 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:18003640 1318579 Fkbp8 FK506 binding protein 8 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:18003640 1318579 Fkbp8 FK506 binding protein 8 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:18003640 1318579 Fkbp8 FK506 binding protein 8 gene MP:0005226 abnormal vertebral arch development IAGP N RGD:5509061 20141003 MGI PMID:18003640 1318579 Fkbp8 FK506 binding protein 8 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17573772 1318579 Fkbp8 FK506 binding protein 8 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18003640 1318579 Fkbp8 FK506 binding protein 8 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15105374 1318579 Fkbp8 FK506 binding protein 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18459960 1318579 Fkbp8 FK506 binding protein 8 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:15105374 1318579 Fkbp8 FK506 binding protein 8 gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20160428 MGI PMID:18003640 1318581 Mtrr 5-methyltetrahydrofolate-homocysteine methyltransferase reductase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17369066 1318581 Mtrr 5-methyltetrahydrofolate-homocysteine methyltransferase reductase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:17369066 1318581 Mtrr 5-methyltetrahydrofolate-homocysteine methyltransferase reductase gene MP:0006076 abnormal circulating homocysteine level IAGP N RGD:5509061 20141003 MGI PMID:17369066 1318581 Mtrr 5-methyltetrahydrofolate-homocysteine methyltransferase reductase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1318581 Mtrr 5-methyltetrahydrofolate-homocysteine methyltransferase reductase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20180920 MGI PMID:17369066 1318581 Mtrr 5-methyltetrahydrofolate-homocysteine methyltransferase reductase gene MP:0030645 decreased circulating methionine level IAGP N RGD:5509061 20180920 MGI PMID:17369066 1318584 Papola poly (A) polymerase alpha gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1318584 Papola poly (A) polymerase alpha gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210826 MGI 1318584 Papola poly (A) polymerase alpha gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220811 MGI 1318584 Papola poly (A) polymerase alpha gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1318584 Papola poly (A) polymerase alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318586 Gng13 guanine nucleotide binding protein (G protein), gamma 13 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 1318586 Gng13 guanine nucleotide binding protein (G protein), gamma 13 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170518 MGI PMID:25416620 1318586 Gng13 guanine nucleotide binding protein (G protein), gamma 13 gene MP:0001924 infertility IAGP N RGD:5509061 20170518 MGI PMID:25416620 1318586 Gng13 guanine nucleotide binding protein (G protein), gamma 13 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:23637188 1318586 Gng13 guanine nucleotide binding protein (G protein), gamma 13 gene MP:0002989 small kidney IEA N RGD:5509061 20160811 MGI 1318586 Gng13 guanine nucleotide binding protein (G protein), gamma 13 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20170518 MGI PMID:25416620 1318586 Gng13 guanine nucleotide binding protein (G protein), gamma 13 gene MP:0005499 abnormal olfactory system morphology IAGP N RGD:5509061 20141003 MGI PMID:23637188 1318586 Gng13 guanine nucleotide binding protein (G protein), gamma 13 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20181227 MGI 1318586 Gng13 guanine nucleotide binding protein (G protein), gamma 13 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:23637188 1318586 Gng13 guanine nucleotide binding protein (G protein), gamma 13 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:23637188 1318586 Gng13 guanine nucleotide binding protein (G protein), gamma 13 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 1318586 Gng13 guanine nucleotide binding protein (G protein), gamma 13 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20160421 MGI 1318586 Gng13 guanine nucleotide binding protein (G protein), gamma 13 gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:23637188 1318593 Tiam2 T cell lymphoma invasion and metastasis 2 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20191003 MGI PMID:30817801 1318595 Rpl11 ribosomal protein L11 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20210401 MGI PMID:26489471 1318595 Rpl11 ribosomal protein L11 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20210401 MGI PMID:26489471 1318595 Rpl11 ribosomal protein L11 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20210325 MGI PMID:26489471 1318595 Rpl11 ribosomal protein L11 gene MP:0001577 anemia IAGP N RGD:5509061 20210325 MGI PMID:26489471 1318595 Rpl11 ribosomal protein L11 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20210401 MGI PMID:26489471 1318595 Rpl11 ribosomal protein L11 gene MP:0002083 premature death IAGP N RGD:5509061 20210325 MGI PMID:26489471 1318595 Rpl11 ribosomal protein L11 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20210325 MGI PMID:26489471 1318595 Rpl11 ribosomal protein L11 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20210401 MGI PMID:26489471 1318595 Rpl11 ribosomal protein L11 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20210401 MGI PMID:26489471 1318595 Rpl11 ribosomal protein L11 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20210401 MGI PMID:26489471 1318595 Rpl11 ribosomal protein L11 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20210401 MGI PMID:26489471 1318595 Rpl11 ribosomal protein L11 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20210325 MGI PMID:26489471 1318595 Rpl11 ribosomal protein L11 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210401 MGI PMID:26489471 1318595 Rpl11 ribosomal protein L11 gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20210325 MGI PMID:26489471 1318598 Mnt max binding protein gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15028671 1318598 Mnt max binding protein gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:15028671 1318598 Mnt max binding protein gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:16740691 1318598 Mnt max binding protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12970171 1318598 Mnt max binding protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12970171 1318598 Mnt max binding protein gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:15028671 1318598 Mnt max binding protein gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12970171 1318598 Mnt max binding protein gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16740691 1318598 Mnt max binding protein gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:15028671 1318598 Mnt max binding protein gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:15028671 1318598 Mnt max binding protein gene MP:0004441 small occipital bone IAGP N RGD:5509061 20141003 MGI PMID:15028671 1318598 Mnt max binding protein gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20141003 MGI PMID:15028671 1318598 Mnt max binding protein gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:15028671 1318598 Mnt max binding protein gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15028671 1318598 Mnt max binding protein gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:15028671 1318598 Mnt max binding protein gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12970171 1318598 Mnt max binding protein gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:16740691 1318598 Mnt max binding protein gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:15028671 1318598 Mnt max binding protein gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15028671 1318598 Mnt max binding protein gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:15028671 1318598 Mnt max binding protein gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12970171 1318598 Mnt max binding protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15028671 1318598 Mnt max binding protein gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15028671 1318601 Ddx23 DEAD box helicase 23 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1318601 Ddx23 DEAD box helicase 23 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318603 Ikzf2 IKAROS family zinc finger 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19620299 1318603 Ikzf2 IKAROS family zinc finger 2 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20160929 MGI PMID:27534441 1318603 Ikzf2 IKAROS family zinc finger 2 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1318603 Ikzf2 IKAROS family zinc finger 2 gene MP:0001967 deafness IAGP N RGD:5509061 20160929 MGI PMID:27534441 1318603 Ikzf2 IKAROS family zinc finger 2 gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20240523 MGI 1318603 Ikzf2 IKAROS family zinc finger 2 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20181882 1318603 Ikzf2 IKAROS family zinc finger 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1318603 Ikzf2 IKAROS family zinc finger 2 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:19620299 1318603 Ikzf2 IKAROS family zinc finger 2 gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20141003 MGI PMID:19620299 1318603 Ikzf2 IKAROS family zinc finger 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19620299 1318603 Ikzf2 IKAROS family zinc finger 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19620299 1318605 Ptp4a3 protein tyrosine phosphatase 4a3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1318605 Ptp4a3 protein tyrosine phosphatase 4a3 gene MP:0000692 small spleen IEA N RGD:5509061 20201022 MGI 1318605 Ptp4a3 protein tyrosine phosphatase 4a3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23555575 1318605 Ptp4a3 protein tyrosine phosphatase 4a3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1318605 Ptp4a3 protein tyrosine phosphatase 4a3 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23555575 1318605 Ptp4a3 protein tyrosine phosphatase 4a3 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23555575 1318605 Ptp4a3 protein tyrosine phosphatase 4a3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23554722 1318605 Ptp4a3 protein tyrosine phosphatase 4a3 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:23555575 1318605 Ptp4a3 protein tyrosine phosphatase 4a3 gene MP:0009084 blind uterus IEA N RGD:5509061 20210128 MGI 1318605 Ptp4a3 protein tyrosine phosphatase 4a3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23555575 1318605 Ptp4a3 protein tyrosine phosphatase 4a3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0000480 increased rib number IEA N RGD:5509061 20160114 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0000600 liver hypoplasia IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0000819 abnormal olfactory bulb morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0000914 exencephaly IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0002191 abnormal artery morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0002237 abnormal nasal cavity morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0002249 abnormal larynx morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0003078 aphakia IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0003387 aorta coarctation IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0004057 thin myocardium compact layer IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0004163 abnormal adenohypophysis morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0004181 abnormal carotid artery morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0004259 small placenta IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318607 Atp11a ATPase, class VI, type 11A gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0005236 abnormal olfactory nerve morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0005287 narrow eye opening IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0005587 abnormal Meckel's cartilage morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318607 Atp11a ATPase, class VI, type 11A gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318607 Atp11a ATPase, class VI, type 11A gene MP:0010912 herniated liver IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318607 Atp11a ATPase, class VI, type 11A gene MP:0011513 abnormal vertebral artery morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20180726 MGI PMID:29799007 1318607 Atp11a ATPase, class VI, type 11A gene MP:0012303 umbilical vein stenosis IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0013237 abnormal skeletal muscle regeneration IAGP N RGD:5509061 20180726 MGI PMID:29799007 1318607 Atp11a ATPase, class VI, type 11A gene MP:0013809 absent pectinate muscle IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0013833 absent olfactory nerve IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0013875 increased trigeminal neuroma incidence IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0013945 abnormal elbow joint morphology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0013968 multiple persisting craniopharyngeal ducts IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0013975 abnormal coronary sinus connection IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0013985 abnormal umbilical vein topology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0014003 additional anastomosis between intracranial vertebral arteries IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0020500 persistent trigeminal artery IEA N RGD:5509061 20180628 MGI 1318607 Atp11a ATPase, class VI, type 11A gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:29539633 1318609 Enpp4 ectonucleotide pyrophosphatase/phosphodiesterase 4 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220519 MGI 1318609 Enpp4 ectonucleotide pyrophosphatase/phosphodiesterase 4 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20201022 MGI 1318612 Galk2 galactokinase 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 1318612 Galk2 galactokinase 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1318612 Galk2 galactokinase 2 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1318612 Galk2 galactokinase 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1318612 Galk2 galactokinase 2 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20181227 MGI 1318612 Galk2 galactokinase 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170105 MGI 1318612 Galk2 galactokinase 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1318612 Galk2 galactokinase 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1318612 Galk2 galactokinase 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20170105 MGI 1318612 Galk2 galactokinase 2 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20211021 MGI 1318612 Galk2 galactokinase 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1318612 Galk2 galactokinase 2 gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20211021 MGI 1318612 Galk2 galactokinase 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1318612 Galk2 galactokinase 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1318618 Swt1 SWT1 RNA endoribonuclease homolog (S. cerevisiae) gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1318618 Swt1 SWT1 RNA endoribonuclease homolog (S. cerevisiae) gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220519 MGI 1318618 Swt1 SWT1 RNA endoribonuclease homolog (S. cerevisiae) gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220519 MGI 1318618 Swt1 SWT1 RNA endoribonuclease homolog (S. cerevisiae) gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220519 MGI 1318618 Swt1 SWT1 RNA endoribonuclease homolog (S. cerevisiae) gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220519 MGI 1318620 Rmdn3 regulator of microtubule dynamics 3 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20200402 MGI PMID:31501572 1318620 Rmdn3 regulator of microtubule dynamics 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1318622 Prkag3 protein kinase, AMP-activated, gamma 3 non-catalytic subunit gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15247217 1318622 Prkag3 protein kinase, AMP-activated, gamma 3 non-catalytic subunit gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20191226 MGI PMID:15247217 1318624 Izumo1r IZUMO1 receptor, JUNO gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20161201 MGI PMID:24739963 1318624 Izumo1r IZUMO1 receptor, JUNO gene MP:0001926 female infertility IAGP N RGD:5509061 20161201 MGI PMID:24739963 1318624 Izumo1r IZUMO1 receptor, JUNO gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141204 MGI PMID:23651732 1318624 Izumo1r IZUMO1 receptor, JUNO gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1318624 Izumo1r IZUMO1 receptor, JUNO gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20210128 MGI 1318624 Izumo1r IZUMO1 receptor, JUNO gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160114 MGI 1318624 Izumo1r IZUMO1 receptor, JUNO gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1318624 Izumo1r IZUMO1 receptor, JUNO gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20170105 MGI 1318624 Izumo1r IZUMO1 receptor, JUNO gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160114 MGI 1318624 Izumo1r IZUMO1 receptor, JUNO gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1318624 Izumo1r IZUMO1 receptor, JUNO gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20170105 MGI 1318627 Prpf39 pre-mRNA processing factor 39 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230119 MGI 1318627 Prpf39 pre-mRNA processing factor 39 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230119 MGI 1318627 Prpf39 pre-mRNA processing factor 39 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1318627 Prpf39 pre-mRNA processing factor 39 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1318627 Prpf39 pre-mRNA processing factor 39 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1318627 Prpf39 pre-mRNA processing factor 39 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1318627 Prpf39 pre-mRNA processing factor 39 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1318627 Prpf39 pre-mRNA processing factor 39 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1318627 Prpf39 pre-mRNA processing factor 39 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20230119 MGI 1318629 Ift27 intraflagellar transport 27 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20151112 MGI PMID:26023097 1318629 Ift27 intraflagellar transport 27 gene MP:0000380 small hair follicles IAGP N RGD:5509061 20151112 MGI PMID:26023097 1318629 Ift27 intraflagellar transport 27 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20151112 MGI PMID:26023097 1318629 Ift27 intraflagellar transport 27 gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0001575 cyanosis IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0001925 male infertility IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0002243 abnormal vomeronasal organ morphology IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0002639 micrognathia IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20151112 MGI PMID:26023097 1318629 Ift27 intraflagellar transport 27 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0003052 omphalocele IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20151112 MGI PMID:26023097 1318629 Ift27 intraflagellar transport 27 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0003950 abnormal plasma membrane morphology IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0004159 double aortic arch IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0004592 small mandible IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0004880 lung cyst IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20151112 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20151112 MGI PMID:26023097 1318629 Ift27 intraflagellar transport 27 gene MP:0009837 abnormal sperm end piece morphology IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0009905 absent tongue IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0010146 umbilical hernia IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0010406 common atrium IAGP N RGD:5509061 20231221 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0010458 pulmonary trunk hypoplasia IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0010853 abnormal lung position or orientation IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20151112 MGI PMID:26023097 1318629 Ift27 intraflagellar transport 27 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0011250 abdominal situs ambiguus IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0011683 dual inferior vena cava IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0012285 misaligned sternebrae IAGP N RGD:5509061 20150611 MGI PMID:25446516 1318629 Ift27 intraflagellar transport 27 gene MP:0014468 disorganized sperm mitochondrial sheath IAGP N RGD:5509061 20240613 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20220217 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0031351 abnormal sperm flagellum thickness IAGP N RGD:5509061 20220317 MGI PMID:28964737 1318629 Ift27 intraflagellar transport 27 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220317 MGI PMID:28964737 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20231207 MGI 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0000731 increased collagen deposition in the muscles IAGP N RGD:5509061 20141003 MGI PMID:23564457 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:23564457 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:24563484 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23564457 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:23564457 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:24563484 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20220519 MGI 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20220519 MGI 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23564457 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:24563484 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0004089 dilated sarcoplasmic reticulum IAGP N RGD:5509061 20141003 MGI PMID:24563484 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:24563484 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0005542 cornea vascularization IEA N RGD:5509061 20231207 MGI 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:23564457 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:24563484 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:23564457 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:24563484 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:23564457 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20141003 MGI PMID:24563484 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:23564457 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:24563484 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0013237 abnormal skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:23564457 1318631 Col6a3 collagen, type VI, alpha 3 gene MP:0030803 abnormal tendon cell morphology IAGP N RGD:5509061 20181011 MGI PMID:24563484 1318636 Atp8b2 ATPase, class I, type 8B, member 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1318636 Atp8b2 ATPase, class I, type 8B, member 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1318636 Atp8b2 ATPase, class I, type 8B, member 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1318636 Atp8b2 ATPase, class I, type 8B, member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1318640 Tm4sf5 transmembrane 4 superfamily member 5 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20211223 MGI PMID:30956113 1318640 Tm4sf5 transmembrane 4 superfamily member 5 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1318640 Tm4sf5 transmembrane 4 superfamily member 5 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20240523 MGI 1318640 Tm4sf5 transmembrane 4 superfamily member 5 gene MP:0011942 decreased fluid intake IEA N RGD:5509061 20230601 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:22488641 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:22488641 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:17106887 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:22511315 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0000963 fused dorsal root ganglion IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0001067 absent mandibular nerve IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:22511315 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:17106887 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0001512 trunk curl IEA N RGD:5509061 20181227 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:22511315 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:19776720 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22511315 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:17106887 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:22488641 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:19776720 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0003130 anal atresia IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19776720 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22511315 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:19776720 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0004175 telangiectasia IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20141003 MGI PMID:22488641 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:17106887 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0004273 abnormal basal lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:19776720 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19776720 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0005299 abnormal eye posterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:17106887 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:19776720 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:22511315 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0005556 abnormal renal filtration rate IAGP N RGD:5509061 20141003 MGI PMID:22488641 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0005581 abnormal renin activity IAGP N RGD:5509061 20141003 MGI PMID:19776720 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0005587 abnormal Meckel's cartilage morphology IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:19776720 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0008817 hematoma IAGP N RGD:5509061 20141003 MGI PMID:17106887 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0008854 bleb IAGP N RGD:5509061 20141003 MGI PMID:22511315 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0008856 fetal bleb IAGP N RGD:5509061 20141003 MGI PMID:17106887 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0009532 decreased parotid gland size IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0010526 aortic arch coarctation IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0010528 pulmonary vein hypoplasia IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22511315 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0010912 herniated liver IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22511315 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17106887 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20141003 MGI PMID:22488641 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011321 abnormal peritubular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:19776720 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22488641 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011376 abnormal kidney corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:22488641 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011437 glomerulus hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011455 absent glomerular endothelium fenestra IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011480 impaired ureteric peristalsis IAGP N RGD:5509061 20141003 MGI PMID:22488641 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011509 dilated glomerular capillary IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011509 dilated glomerular capillary IAGP N RGD:5509061 20141003 MGI PMID:19776720 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011565 kidney papillary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22488641 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:19776720 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:22488641 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20141003 MGI PMID:17460146 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011854 cerebral edema IAGP N RGD:5509061 20141003 MGI PMID:17106887 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011856 abnormal glomerular filtration barrier function IAGP N RGD:5509061 20141003 MGI PMID:19776720 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011857 short kidney papilla IAGP N RGD:5509061 20141003 MGI PMID:22488641 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011859 decreased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:19776720 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0011860 abnormal peritubular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19776720 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0013814 abnormal hepatic portal vein connection IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0013852 abnormal Mullerian duct topology IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0013880 absent ductus venosus IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0013932 fragmented Meckel's cartilage IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0013970 absent connection between subcutaneous lymph vessels and lymph sac IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0014000 anastomosis between internal carotid artery and basilar artery IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0014006 absent posterior communicating artery IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0014087 retrolental blood IEA N RGD:5509061 20180628 MGI 1318642 Crim1 cysteine rich transmembrane BMP regulator 1 gene MP:0031428 lens dislocation IEA N RGD:5509061 20220714 MGI 1318645 Guca1a guanylate cyclase activator 1a (retina) gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23082185 1318645 Guca1a guanylate cyclase activator 1a (retina) gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:21464903 1318645 Guca1a guanylate cyclase activator 1a (retina) gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:23082185 1318645 Guca1a guanylate cyclase activator 1a (retina) gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11493703 1318645 Guca1a guanylate cyclase activator 1a (retina) gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21123569 1318645 Guca1a guanylate cyclase activator 1a (retina) gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21464903 1318645 Guca1a guanylate cyclase activator 1a (retina) gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23082185 1318645 Guca1a guanylate cyclase activator 1a (retina) gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21464903 1318645 Guca1a guanylate cyclase activator 1a (retina) gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11493703 1318645 Guca1a guanylate cyclase activator 1a (retina) gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15173221 1318645 Guca1a guanylate cyclase activator 1a (retina) gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21464903 1318645 Guca1a guanylate cyclase activator 1a (retina) gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:21464903 1318645 Guca1a guanylate cyclase activator 1a (retina) gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21464903 1318645 Guca1a guanylate cyclase activator 1a (retina) gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21464903 1318645 Guca1a guanylate cyclase activator 1a (retina) gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:21464903 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20150305 MGI PMID:19160489 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20150305 MGI PMID:19160489 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20150305 MGI PMID:19160489 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190808 MGI 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20150305 MGI PMID:19160489 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20150305 MGI PMID:19160489 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0001714 absent trophoblast giant cells IAGP N RGD:5509061 20141003 MGI PMID:20530197 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0001714 absent trophoblast giant cells IAGP N RGD:5509061 20150305 MGI PMID:19160489 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:20530197 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0003708 binucleate IAGP N RGD:5509061 20150305 MGI PMID:19160489 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20150305 MGI PMID:19160489 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20150305 MGI PMID:19160489 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20190808 MGI 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0004259 small placenta IAGP N RGD:5509061 20150305 MGI PMID:19160489 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0004266 pale placenta IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:19861496 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20530197 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18552834 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20530197 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20150305 MGI PMID:19160489 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318647 Fzr1 fizzy and cell division cycle 20 related 1 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:20530197 1318649 Trim36 tripartite motif-containing 36 gene MP:0001925 male infertility IAGP N RGD:5509061 20210729 MGI PMID:32311190 1318649 Trim36 tripartite motif-containing 36 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38697008 1318649 Trim36 tripartite motif-containing 36 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210729 MGI PMID:32311190 1318652 Tasor transcription activation suppressor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20150910 MGI PMID:19099580 1318652 Tasor transcription activation suppressor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20150910 MGI PMID:24781204 1318652 Tasor transcription activation suppressor gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1318652 Tasor transcription activation suppressor gene MP:0009455 enhanced cued conditioning behavior IEA N RGD:5509061 20220811 MGI 1318652 Tasor transcription activation suppressor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318652 Tasor transcription activation suppressor gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20150910 MGI PMID:24781204 1318652 Tasor transcription activation suppressor gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1318652 Tasor transcription activation suppressor gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:24781204 1318654 Gart phosphoribosylglycinamide formyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1318654 Gart phosphoribosylglycinamide formyltransferase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1318654 Gart phosphoribosylglycinamide formyltransferase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0000745 tremors IEA N RGD:5509061 20181227 MGI 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0001394 circling IAGP N RGD:5509061 20240328 MGI PMID:37001993 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20160421 MGI 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0001513 limb grasping IEA N RGD:5509061 20160421 MGI 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20240328 MGI PMID:37001993 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20201022 MGI 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20180830 MGI PMID:29084757 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0001967 deafness IAGP N RGD:5509061 20180830 MGI PMID:29084757 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20160421 MGI 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20180830 MGI PMID:29084757 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20180830 MGI PMID:29084757 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0004413 absent cochlear microphonics IAGP N RGD:5509061 20180830 MGI PMID:29084757 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20180830 MGI PMID:29084757 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20240328 MGI PMID:29255404 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20240328 MGI PMID:37001993 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20240328 MGI PMID:29255404 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20240328 MGI PMID:37001993 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0004517 decreased vestibular hair cell stereocilia number IAGP N RGD:5509061 20240328 MGI PMID:37001993 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20240328 MGI PMID:29255404 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20240328 MGI PMID:29255404 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20240328 MGI PMID:29255404 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20180830 MGI PMID:29084757 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20160421 MGI 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0011061 abnormal inner hair cell kinocilium morphology IAGP N RGD:5509061 20240328 MGI PMID:29255404 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20180830 MGI PMID:29084757 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20240328 MGI PMID:29255404 1318656 Cib2 calcium and integrin binding family member 2 gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:29255404 1318657 Ktn1 kinectin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11486041 1318658 Pxdn peroxidasin gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0000373 belly spot IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0000585 kinked tail IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0001293 anophthalmia IEA N RGD:5509061 20240523 MGI 1318658 Pxdn peroxidasin gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0001306 small lens IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1318658 Pxdn peroxidasin gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1318658 Pxdn peroxidasin gene MP:0002574 increased vertical activity IEA N RGD:5509061 20200402 MGI 1318658 Pxdn peroxidasin gene MP:0002579 disorganized secondary lens fibers IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0005299 abnormal eye posterior chamber morphology IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0006200 vitreous body deposition IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0009392 retina gliosis IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0009742 increased cornea stroma thickness IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1318658 Pxdn peroxidasin gene MP:0010235 abnormal retina inner limiting membrane morphology IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0010709 absent eye anterior chamber IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0010713 corneal-lenticular stalk IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1318658 Pxdn peroxidasin gene MP:0013258 abnormal extracellular matrix morphology IAGP N RGD:5509061 20141009 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0013743 ciliary body hypoplasia IAGP N RGD:5509061 20150416 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1318658 Pxdn peroxidasin gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:24895407 1318658 Pxdn peroxidasin gene MP:0031212 decreased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:24895407 1318660 Tspan32 tetraspanin 32 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210826 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220811 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0001200 thick skin IEA N RGD:5509061 20210826 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210520 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20221215 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0003883 enlarged stomach IEA N RGD:5509061 20210826 MGI 1318660 Tspan32 tetraspanin 32 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12077330 1318665 Dhx29 DExH-box helicase 29 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1318665 Dhx29 DExH-box helicase 29 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20181227 MGI 1318665 Dhx29 DExH-box helicase 29 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20181227 MGI 1318665 Dhx29 DExH-box helicase 29 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1318665 Dhx29 DExH-box helicase 29 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1318665 Dhx29 DExH-box helicase 29 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20231207 MGI 1318665 Dhx29 DExH-box helicase 29 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20141003 MGI 1318665 Dhx29 DExH-box helicase 29 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318665 Dhx29 DExH-box helicase 29 gene MP:0011435 increased urine magnesium level IEA N RGD:5509061 20181227 MGI 1318671 Apobec2 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20111116 MGI 1318671 Apobec2 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 gene MP:0000751 myopathy IAGP N RGD:5509061 20150910 MGI PMID:20022958 1318671 Apobec2 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150910 MGI PMID:20022958 1318671 Apobec2 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 gene MP:0001732 postnatal growth retardation IEA N RGD:5509061 20111116 MGI 1318671 Apobec2 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16055735 1318671 Apobec2 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20150910 MGI PMID:20022958 1318671 Apobec2 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20150910 MGI PMID:20022958 1318671 Apobec2 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20150910 MGI PMID:20022958 1318671 Apobec2 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20150910 MGI PMID:20022958 1318671 Apobec2 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 gene MP:0009426 decreased soleus weight IAGP N RGD:5509061 20150910 MGI PMID:20022958 1318671 Apobec2 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 gene MP:0009428 decreased tibialis anterior weight IAGP N RGD:5509061 20150910 MGI PMID:20022958 1318671 Apobec2 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20111116 MGI 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20230119 MGI 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0001262 decreased body weight IEA N RGD:5509061 20230119 MGI 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230119 MGI 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:12393861 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:12393861 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20141003 MGI PMID:12393861 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0002648 delaminated enamel IAGP N RGD:5509061 20141003 MGI PMID:12393861 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0002649 abnormal enamel rod pattern IAGP N RGD:5509061 20141003 MGI PMID:12393861 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:12393861 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230119 MGI 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20230119 MGI 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20230119 MGI 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20240523 MGI 1318676 Mmp20 matrix metallopeptidase 20 (enamelysin) gene MP:0013129 abnormal tooth color IEA N RGD:5509061 20230119 MGI 1318682 Plbd1 phospholipase B domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160915 MGI PMID:24652767 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000274 enlarged heart IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:21668589 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000458 abnormal mandible morphology IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:15630138 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0000745 tremors IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15630138 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0001293 anophthalmia IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19118178 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19118178 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:19118178 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0001891 hydrocephaly IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:19118178 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:15630138 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20141003 MGI PMID:15630138 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:19118178 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0002802 abnormal discrimination learning IAGP N RGD:5509061 20141003 MGI PMID:19118178 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:19118178 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:19118178 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20221215 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15630138 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0003917 increased kidney weight IEA N RGD:5509061 20240523 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0004609 vertebral fusion IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15630138 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0005270 abnormal zygomatic bone morphology IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20220519 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0008039 increased NK T cell number IEA N RGD:5509061 20211021 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:19118178 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:21668589 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20240627 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20211021 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20211021 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0011496 abnormal head size IEA N RGD:5509061 20210826 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0013520 increased CD4-positive NK T cell number IEA N RGD:5509061 20211021 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0013523 increased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20211021 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20211021 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1318684 Spred1 sprouty protein with EVH-1 domain 1, related sequence gene MP:0030066 short face IAGP N RGD:5509061 20171019 MGI PMID:15630138 1318686 Hmgn5 high-mobility group nucleosome binding domain 5 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141030 MGI PMID:23620591 1318686 Hmgn5 high-mobility group nucleosome binding domain 5 gene MP:0001586 abnormal erythrocyte cell number IAGP N RGD:5509061 20141030 MGI PMID:23620591 1318686 Hmgn5 high-mobility group nucleosome binding domain 5 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141030 MGI PMID:23620591 1318686 Hmgn5 high-mobility group nucleosome binding domain 5 gene MP:0001958 emphysema IAGP N RGD:5509061 20141030 MGI PMID:23620591 1318686 Hmgn5 high-mobility group nucleosome binding domain 5 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141030 MGI 1318686 Hmgn5 high-mobility group nucleosome binding domain 5 gene MP:0002297 abnormal forced expiratory flow rates IAGP N RGD:5509061 20141030 MGI PMID:23620591 1318686 Hmgn5 high-mobility group nucleosome binding domain 5 gene MP:0002304 abnormal total lung capacity IAGP N RGD:5509061 20141030 MGI PMID:23620591 1318686 Hmgn5 high-mobility group nucleosome binding domain 5 gene MP:0002311 abnormal inspiratory capacity IAGP N RGD:5509061 20141030 MGI PMID:23620591 1318686 Hmgn5 high-mobility group nucleosome binding domain 5 gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20141030 MGI PMID:23620591 1318686 Hmgn5 high-mobility group nucleosome binding domain 5 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141030 MGI PMID:23620591 1318686 Hmgn5 high-mobility group nucleosome binding domain 5 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141030 MGI PMID:23620591 1318686 Hmgn5 high-mobility group nucleosome binding domain 5 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141030 MGI PMID:23620591 1318686 Hmgn5 high-mobility group nucleosome binding domain 5 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141030 MGI PMID:23620591 1318686 Hmgn5 high-mobility group nucleosome binding domain 5 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141030 MGI PMID:23620591 1318688 Pias4 protein inhibitor of activated STAT 4 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15528356 1318688 Pias4 protein inhibitor of activated STAT 4 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15169916 1318688 Pias4 protein inhibitor of activated STAT 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15169916 1318688 Pias4 protein inhibitor of activated STAT 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15528356 1318691 Ctu1 cytosolic thiouridylase subunit 1 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1318691 Ctu1 cytosolic thiouridylase subunit 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1318694 Ern2 endoplasmic reticulum to nucleus signalling 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:11238559 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17531978 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:20346937 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0000140 absent vertebral pedicles IAGP N RGD:5509061 20141003 MGI PMID:17360776 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0000140 absent vertebral pedicles IAGP N RGD:5509061 20141003 MGI PMID:20346937 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0000152 absent proximal rib IAGP N RGD:5509061 20141003 MGI PMID:17360776 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:17531978 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:17531978 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:17360776 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:17531978 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17360776 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:17531978 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:17360776 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17531978 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:17531978 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0003939 abnormal myotome morphology IAGP N RGD:5509061 20141003 MGI PMID:17360776 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:17531978 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0004604 abnormal vertebral pedicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17531978 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0004604 abnormal vertebral pedicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20346937 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:17531978 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:17360776 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:17531978 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:20346937 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17360776 1318698 Ripply2 ripply transcriptional repressor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17531978 1318701 Lhx8 LIM homeobox protein 8 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:15217369 1318701 Lhx8 LIM homeobox protein 8 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:15978004 1318701 Lhx8 LIM homeobox protein 8 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:12855770 1318701 Lhx8 LIM homeobox protein 8 gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12855770 1318701 Lhx8 LIM homeobox protein 8 gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15217369 1318701 Lhx8 LIM homeobox protein 8 gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15978004 1318701 Lhx8 LIM homeobox protein 8 gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22315402 1318701 Lhx8 LIM homeobox protein 8 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220421 MGI PMID:18509161 1318701 Lhx8 LIM homeobox protein 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15978004 1318701 Lhx8 LIM homeobox protein 8 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15978004 1318701 Lhx8 LIM homeobox protein 8 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15978004 1318701 Lhx8 LIM homeobox protein 8 gene MP:0001926 female infertility IAGP N RGD:5509061 20220421 MGI PMID:18509161 1318701 Lhx8 LIM homeobox protein 8 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20230518 MGI PMID:32086523 1318701 Lhx8 LIM homeobox protein 8 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10611327 1318701 Lhx8 LIM homeobox protein 8 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20220421 MGI PMID:18509161 1318701 Lhx8 LIM homeobox protein 8 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22315402 1318701 Lhx8 LIM homeobox protein 8 gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22315402 1318701 Lhx8 LIM homeobox protein 8 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:22315402 1318701 Lhx8 LIM homeobox protein 8 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22315402 1318701 Lhx8 LIM homeobox protein 8 gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:15978004 1318701 Lhx8 LIM homeobox protein 8 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20220421 MGI PMID:18509161 1318701 Lhx8 LIM homeobox protein 8 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20220421 MGI PMID:18509161 1318701 Lhx8 LIM homeobox protein 8 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20220421 MGI PMID:18509161 1318701 Lhx8 LIM homeobox protein 8 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20220421 MGI PMID:29329412 1318701 Lhx8 LIM homeobox protein 8 gene MP:0009085 abnormal uterine horn morphology IAGP N RGD:5509061 20220421 MGI PMID:18509161 1318701 Lhx8 LIM homeobox protein 8 gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20220421 MGI PMID:18509161 1318701 Lhx8 LIM homeobox protein 8 gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20220421 MGI PMID:29329412 1318701 Lhx8 LIM homeobox protein 8 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:10611327 1318701 Lhx8 LIM homeobox protein 8 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:10611327 1318701 Lhx8 LIM homeobox protein 8 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:22315402 1318701 Lhx8 LIM homeobox protein 8 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20220421 MGI PMID:29329412 1318701 Lhx8 LIM homeobox protein 8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20220421 MGI PMID:29329412 1318701 Lhx8 LIM homeobox protein 8 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10611327 1318701 Lhx8 LIM homeobox protein 8 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15217369 1318701 Lhx8 LIM homeobox protein 8 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15978004 1318701 Lhx8 LIM homeobox protein 8 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220421 MGI PMID:18509161 1318701 Lhx8 LIM homeobox protein 8 gene MP:0011122 absent primordial ovarian follicles IAGP N RGD:5509061 20220421 MGI PMID:18509161 1318701 Lhx8 LIM homeobox protein 8 gene MP:0013507 increased ovary apoptosis IAGP N RGD:5509061 20220421 MGI PMID:29329412 1318701 Lhx8 LIM homeobox protein 8 gene MP:0013607 ovary fibrosis IAGP N RGD:5509061 20220421 MGI PMID:29329412 1318701 Lhx8 LIM homeobox protein 8 gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20220421 MGI PMID:29329412 1318701 Lhx8 LIM homeobox protein 8 gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20220421 MGI PMID:29329412 1318701 Lhx8 LIM homeobox protein 8 gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20220421 MGI PMID:29329412 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:14745449 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:14745449 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0000947 convulsive seizures IEA N RGD:5509061 20221110 MGI 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0001136 dilated uterine cervix IAGP N RGD:5509061 20141003 MGI PMID:14745449 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:14745449 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20200521 MGI PMID:24425853 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20221110 MGI 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20200521 MGI PMID:24425853 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20200521 MGI PMID:24425853 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20200521 MGI PMID:24425853 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:14745449 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20221110 MGI 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0005577 uterus prolapse IAGP N RGD:5509061 20141003 MGI PMID:14745449 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0008418 abnormal cutaneous elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:14745449 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0010252 anterior subcapsular cataract IAGP N RGD:5509061 20200521 MGI PMID:24425853 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:14745449 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20221110 MGI 1318706 Loxl1 lysyl oxidase-like 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20221110 MGI 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0002653 abnormal ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0003588 ureter stenosis IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318708 Dlg5 discs large MAGUK scaffold protein 5 gene MP:0011331 abnormal papillary duct morphology IAGP N RGD:5509061 20141003 MGI PMID:17765678 1318714 Hgd homogentisate 1, 2-dioxygenase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:10518553 1318714 Hgd homogentisate 1, 2-dioxygenase gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:10518553 1318714 Hgd homogentisate 1, 2-dioxygenase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10518553 1318714 Hgd homogentisate 1, 2-dioxygenase gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:10518553 1318714 Hgd homogentisate 1, 2-dioxygenase gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:10518553 1318714 Hgd homogentisate 1, 2-dioxygenase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10518553 1318714 Hgd homogentisate 1, 2-dioxygenase gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:10518553 1318714 Hgd homogentisate 1, 2-dioxygenase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:10518553 1318714 Hgd homogentisate 1, 2-dioxygenase gene MP:0003619 abnormal urine color IAGP N RGD:5509061 20141003 MGI PMID:8188247 1318714 Hgd homogentisate 1, 2-dioxygenase gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20200528 MGI PMID:31600782 1318714 Hgd homogentisate 1, 2-dioxygenase gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20200528 MGI PMID:31600782 1318714 Hgd homogentisate 1, 2-dioxygenase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20200528 MGI PMID:31600782 1318714 Hgd homogentisate 1, 2-dioxygenase gene MP:0013723 increased circulating tyrosine level IAGP N RGD:5509061 20150409 MGI PMID:10518553 1318714 Hgd homogentisate 1, 2-dioxygenase gene MP:0030619 homogentisic aciduria IAGP N RGD:5509061 20180906 MGI PMID:8188247 1318714 Hgd homogentisate 1, 2-dioxygenase gene MP:0030619 homogentisic aciduria IAGP N RGD:5509061 20200528 MGI PMID:31600782 1318716 Igsf11 immunoglobulin superfamily, member 11 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1318716 Igsf11 immunoglobulin superfamily, member 11 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20170601 MGI PMID:26595655 1318716 Igsf11 immunoglobulin superfamily, member 11 gene MP:0001513 limb grasping IEA N RGD:5509061 20210520 MGI 1318716 Igsf11 immunoglobulin superfamily, member 11 gene MP:0001523 impaired righting response IEA N RGD:5509061 20210520 MGI 1318716 Igsf11 immunoglobulin superfamily, member 11 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1318716 Igsf11 immunoglobulin superfamily, member 11 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20170601 MGI PMID:26595655 1318716 Igsf11 immunoglobulin superfamily, member 11 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0000024 lowered ear position IAGP N RGD:5509061 20151224 MGI PMID:24700590 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0000088 short mandible IAGP N RGD:5509061 20151224 MGI PMID:24700590 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20151224 MGI PMID:24700590 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20151224 MGI PMID:24700590 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20151224 MGI PMID:24700590 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:24700590 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0003036 vertebral transformation IEA N RGD:5509061 20181227 MGI 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20151224 MGI PMID:24700590 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0004592 small mandible IAGP N RGD:5509061 20151224 MGI PMID:24700590 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20181227 MGI 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0006411 upturned snout IAGP N RGD:5509061 20151224 MGI PMID:24700590 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20151224 MGI PMID:24700590 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0011262 abnormal pharyngeal arch mesenchyme morphology IAGP N RGD:5509061 20151224 MGI PMID:24700590 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0012523 abnormal upper lip morphology IAGP N RGD:5509061 20151224 MGI PMID:24700590 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0012760 decreased cranial neural crest cell proliferation IAGP N RGD:5509061 20151224 MGI PMID:24700590 1318718 Mau2 MAU2 sister chromatid cohesion factor gene MP:0030065 face hypoplasia IAGP N RGD:5509061 20170921 MGI PMID:24700590 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:16138077 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16138077 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000608 dissociated hepatocytes IAGP N RGD:5509061 20141003 MGI PMID:16138077 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000745 tremors IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20230907 MGI PMID:37219662 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000917 obstructive hydrocephaly IAGP N RGD:5509061 20230907 MGI PMID:37219662 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16099835 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:16099835 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0001394 circling IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0001412 excessive scratching IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200402 MGI 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:11263494 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:11313485 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409406 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11095756 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11313485 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14630919 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16099835 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11263494 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17409406 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16099835 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002064 seizures IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002715 decreased glycogen catabolism rate IAGP N RGD:5509061 20141003 MGI PMID:16138077 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0002958 cerebral aqueductal stenosis IAGP N RGD:5509061 20230907 MGI PMID:37219662 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:11263494 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:11313485 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:16099835 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16138077 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0005323 dystonia IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20230907 MGI PMID:37219662 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0008018 increased facial tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16099835 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0008021 increased blastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16099835 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20230907 MGI PMID:37219662 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0009275 bruising IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16099835 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11263494 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0010391 increased rhabdomyoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:16138077 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16138077 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16099835 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11313485 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11095756 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11263494 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20230907 MGI PMID:37219662 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:11313485 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0012118 absent trophectoderm cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11313485 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0012119 increased trophectoderm apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11263494 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12450796 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0012690 abnormal stride length IAGP N RGD:5509061 20160609 MGI PMID:26363008 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:17409406 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0030973 impaired gluconeogenesis IAGP N RGD:5509061 20191226 MGI PMID:16138077 1318722 Smarcb1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 gene MP:0031154 intestinal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:12450796 1318723 Gprin1 G protein-regulated inducer of neurite outgrowth 1 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20240523 MGI 1318725 Cmtm3 CKLF-like MARVEL transmembrane domain containing 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20230817 MGI PMID:37229825 1318725 Cmtm3 CKLF-like MARVEL transmembrane domain containing 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20230817 MGI PMID:37229825 1318725 Cmtm3 CKLF-like MARVEL transmembrane domain containing 3 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20230817 MGI PMID:37229825 1318725 Cmtm3 CKLF-like MARVEL transmembrane domain containing 3 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20230817 MGI PMID:37229825 1318725 Cmtm3 CKLF-like MARVEL transmembrane domain containing 3 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20230817 MGI PMID:37229825 1318725 Cmtm3 CKLF-like MARVEL transmembrane domain containing 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20230817 MGI PMID:37229825 1318725 Cmtm3 CKLF-like MARVEL transmembrane domain containing 3 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20230817 MGI PMID:37229825 1318725 Cmtm3 CKLF-like MARVEL transmembrane domain containing 3 gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20230817 MGI PMID:37229825 1318725 Cmtm3 CKLF-like MARVEL transmembrane domain containing 3 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20230817 MGI PMID:37229825 1318725 Cmtm3 CKLF-like MARVEL transmembrane domain containing 3 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20230817 MGI PMID:37229825 1318725 Cmtm3 CKLF-like MARVEL transmembrane domain containing 3 gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240718 MGI PMID:37229825 1318725 Cmtm3 CKLF-like MARVEL transmembrane domain containing 3 gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20230817 MGI PMID:37229825 1318725 Cmtm3 CKLF-like MARVEL transmembrane domain containing 3 gene MP:0021161 increased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20230817 MGI PMID:37229825 1318725 Cmtm3 CKLF-like MARVEL transmembrane domain containing 3 gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20230817 MGI PMID:37229825 1318727 Psph phosphoserine phosphatase gene MP:0000104 abnormal sphenoid bone morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000141 abnormal vertebral body morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000154 rib fusion IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201231 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20201231 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000480 increased rib number IEA N RGD:5509061 20160114 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000565 oligodactyly IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000613 abnormal salivary gland morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000614 absent salivary gland IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000618 small salivary gland IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000632 abnormal pineal gland morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000705 athymia IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000819 abnormal olfactory bulb morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000820 abnormal choroid plexus morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0000897 abnormal midbrain morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0001064 absent trochlear nerve IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1318727 Psph phosphoserine phosphatase gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1318727 Psph phosphoserine phosphatase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1318727 Psph phosphoserine phosphatase gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318727 Psph phosphoserine phosphatase gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1318727 Psph phosphoserine phosphatase gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1318727 Psph phosphoserine phosphatase gene MP:0002015 epithelioid cyst IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20201231 MGI 1318727 Psph phosphoserine phosphatase gene MP:0002177 abnormal outer ear morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0002199 abnormal brain commissure morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0002237 abnormal nasal cavity morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0002239 abnormal nasal septum morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0002243 abnormal vomeronasal organ morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0002249 abnormal larynx morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0002428 abnormal semicircular canal morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20181227 MGI 1318727 Psph phosphoserine phosphatase gene MP:0002768 small adrenal glands IEA N RGD:5509061 20160811 MGI 1318727 Psph phosphoserine phosphatase gene MP:0002858 abnormal posterior semicircular canal morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0002928 abnormal bile duct morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0002989 small kidney IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0003078 aphakia IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20160421 MGI 1318727 Psph phosphoserine phosphatase gene MP:0003262 intestinal/bowel diverticulum IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0003387 aorta coarctation IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0003451 absent olfactory bulb IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0003717 pallor IEA N RGD:5509061 20201231 MGI 1318727 Psph phosphoserine phosphatase gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20220519 MGI 1318727 Psph phosphoserine phosphatase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318727 Psph phosphoserine phosphatase gene MP:0004163 abnormal adenohypophysis morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0004164 abnormal neurohypophysis morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0004201 fetal growth retardation IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0004259 small placenta IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318727 Psph phosphoserine phosphatase gene MP:0004266 pale placenta IEA N RGD:5509061 20210520 MGI 1318727 Psph phosphoserine phosphatase gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0004539 absent maxilla IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0004612 fusion of vertebral bodies IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0004666 absent stapedial artery IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318727 Psph phosphoserine phosphatase gene MP:0005105 abnormal middle ear ossicle morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0005157 holoprosencephaly IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0005236 abnormal olfactory nerve morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20220519 MGI 1318727 Psph phosphoserine phosphatase gene MP:0006033 abnormal external auditory canal morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0006254 thin cerebral cortex IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0008128 abnormal brain internal capsule morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0008129 absent brain internal capsule IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318727 Psph phosphoserine phosphatase gene MP:0008923 thoracoschisis IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0009688 abnormal spinal cord central canal morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0009707 absent external auditory canal IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0009771 absent optic chiasm IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0009904 tongue hypoplasia IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0009905 absent tongue IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0010912 herniated liver IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318727 Psph phosphoserine phosphatase gene MP:0012303 umbilical vein stenosis IEA N RGD:5509061 20180628 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013247 placenta necrosis IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318727 Psph phosphoserine phosphatase gene MP:0013362 absent pineal gland IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013595 absent vomeronasal organ IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013818 abnormal oral cavity morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013833 absent olfactory nerve IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013848 subcutaneous edema IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318727 Psph phosphoserine phosphatase gene MP:0013849 absent abducens nerve IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013850 absent posterior commissure IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013855 absent celiac artery IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013875 increased trigeminal neuroma incidence IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013878 abnormal ductus venosus valve topology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013926 absent neurohypophysis IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013927 abnormal facial nerve topology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013929 absent eye muscles IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013932 fragmented Meckel's cartilage IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013933 short Meckel's cartilage IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013935 basal brain tissue herniation IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013936 abnormal thymus topology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013948 intraembryonal intestine elongation IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013950 abnormal dorsal root ganglion topology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013970 absent connection between subcutaneous lymph vessels and lymph sac IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013980 abnormal pulmonary artery origin IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013988 absent portal vein segment IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013994 abnormal parasellar internal carotid artery branch morphology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0013996 abnormal vertebral artery origin IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0014009 anastomosis between middle cerebral arteries IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0014019 embryo cyst IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0014022 abnormal duodenum topology IEA N RGD:5509061 20170504 MGI 1318727 Psph phosphoserine phosphatase gene MP:0020500 persistent trigeminal artery IEA N RGD:5509061 20180628 MGI 1318727 Psph phosphoserine phosphatase gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:29539633 1318729 Sox12 SRY (sex determining region Y)-box 12 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 1318729 Sox12 SRY (sex determining region Y)-box 12 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:20596238 1318729 Sox12 SRY (sex determining region Y)-box 12 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 1318729 Sox12 SRY (sex determining region Y)-box 12 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:20596238 1318729 Sox12 SRY (sex determining region Y)-box 12 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 1318729 Sox12 SRY (sex determining region Y)-box 12 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18505825 1318729 Sox12 SRY (sex determining region Y)-box 12 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20596238 1318729 Sox12 SRY (sex determining region Y)-box 12 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:20596238 1318729 Sox12 SRY (sex determining region Y)-box 12 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20596238 1318729 Sox12 SRY (sex determining region Y)-box 12 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:20596238 1318729 Sox12 SRY (sex determining region Y)-box 12 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 1318729 Sox12 SRY (sex determining region Y)-box 12 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:20596238 1318729 Sox12 SRY (sex determining region Y)-box 12 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20596238 1318729 Sox12 SRY (sex determining region Y)-box 12 gene MP:0011261 abnormal limb mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 1318731 Irf9 interferon regulatory factor 9 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12923053 1318731 Irf9 interferon regulatory factor 9 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:11114377 1318731 Irf9 interferon regulatory factor 9 gene MP:0002418 increased susceptibility to viral infection IAGP N RGD:5509061 20141003 MGI PMID:9078371 1318731 Irf9 interferon regulatory factor 9 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11070172 1318731 Irf9 interferon regulatory factor 9 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:15800576 1318731 Irf9 interferon regulatory factor 9 gene MP:0008575 increased circulating interferon-beta level IEA N RGD:5509061 20161201 MGI 1318731 Irf9 interferon regulatory factor 9 gene MP:0012556 increased cell death IEA N RGD:5509061 20161201 MGI 1318733 Dhx36 DEAH-box helicase 36 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20150409 MGI PMID:22422825 1318733 Dhx36 DEAH-box helicase 36 gene MP:0013704 increased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20150409 MGI PMID:22422825 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:11950998 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:11950998 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:11950998 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:11950998 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000548 long limbs IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:7675086 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16904611 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16904611 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:18790090 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:18790090 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:18790090 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18790090 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:11950998 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18790090 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16117793 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:16904611 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16904611 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11950998 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16904611 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7675086 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7675086 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11950998 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16904611 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:18790090 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:8751968 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:18790090 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:7675085 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18790090 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:7675085 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:7675086 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10837020 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10837020 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:12531021 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16117793 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12531021 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:18790090 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0002879 increased cellular sensitivity to X-ray irradiation IAGP N RGD:5509061 20141003 MGI PMID:11950998 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11960916 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:7675086 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:11950998 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10383746 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12531021 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7675086 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:21151170 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:7675085 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:12531021 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:16904611 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:7675085 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18790090 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:11950998 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8751968 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16904611 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11960916 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:10383746 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:11950998 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:7675085 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20190829 MGI PMID:8751968 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:11950998 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19114557 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0009387 abnormal epidermal pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16117793 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12531021 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7675085 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0009796 abnormal base-excision repair IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0009796 abnormal base-excision repair IAGP N RGD:5509061 20141003 MGI PMID:7675085 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:10651981 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0010289 increased urinary system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21151170 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12531021 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16117793 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0010699 dilated hair follicle IAGP N RGD:5509061 20181129 MGI PMID:11950998 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10383746 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11950998 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16904611 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22174697 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11950998 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7675086 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20141003 MGI PMID:17326724 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18790090 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12531021 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0013551 decreased cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20161201 MGI PMID:11687625 1318736 Xpa xeroderma pigmentosum, complementation group A gene MP:0030003 hippocampus atrophy IAGP N RGD:5509061 20170706 MGI PMID:22174697 1318738 Mrps25 mitochondrial ribosomal protein S25 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 1318738 Mrps25 mitochondrial ribosomal protein S25 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191128 MGI 1318738 Mrps25 mitochondrial ribosomal protein S25 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1318738 Mrps25 mitochondrial ribosomal protein S25 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1318738 Mrps25 mitochondrial ribosomal protein S25 gene MP:0002582 disorganized extraembryonic tissue IEA N RGD:5509061 20191128 MGI 1318738 Mrps25 mitochondrial ribosomal protein S25 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1318738 Mrps25 mitochondrial ribosomal protein S25 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20160811 MGI 1318738 Mrps25 mitochondrial ribosomal protein S25 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1318738 Mrps25 mitochondrial ribosomal protein S25 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1318738 Mrps25 mitochondrial ribosomal protein S25 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1318738 Mrps25 mitochondrial ribosomal protein S25 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318738 Mrps25 mitochondrial ribosomal protein S25 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20160804 MGI 1318738 Mrps25 mitochondrial ribosomal protein S25 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1318741 Vwa8 von Willebrand factor A domain containing 8 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1318741 Vwa8 von Willebrand factor A domain containing 8 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1318741 Vwa8 von Willebrand factor A domain containing 8 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1318741 Vwa8 von Willebrand factor A domain containing 8 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20160421 MGI 1318741 Vwa8 von Willebrand factor A domain containing 8 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1318741 Vwa8 von Willebrand factor A domain containing 8 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0000495 abnormal colon morphology IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23569244 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0002581 abnormal ileum morphology IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0005005 abnormal self tolerance IAGP N RGD:5509061 20141003 MGI PMID:23569244 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23569244 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23569244 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0008039 increased NK T cell number IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23569244 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17540904 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23569244 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:23569244 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0013520 increased CD4-positive NK T cell number IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0013523 increased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0013763 increased T-helper cell number IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0013771 decreased effector memory T-helper cell number IEA N RGD:5509061 20230601 MGI 1318742 Psmb11 proteasome (prosome, macropain) subunit, beta type, 11 gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20230601 MGI 1318743 Slc25a40 solute carrier family 25, member 40 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18799693 1318744 4921536K21Rik RIKEN cDNA 4921536K21 gene gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1318744 4921536K21Rik RIKEN cDNA 4921536K21 gene gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20180315 MGI PMID:27040500 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20180315 MGI PMID:27040500 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20180315 MGI PMID:27040500 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20180315 MGI PMID:27040500 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0006205 embryonic lethality between implantation and somite formation IAGP N RGD:5509061 20180315 MGI PMID:27040500 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20180315 MGI PMID:27040500 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20180315 MGI PMID:27040500 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20180315 MGI PMID:27040500 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180315 MGI PMID:27040500 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20190411 MGI PMID:27040500 1318749 Upf3a UPF3 regulator of nonsense transcripts homolog A (yeast) gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20180315 MGI PMID:27040500 1318752 Arhgap33 Rho GTPase activating protein 33 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:22810622 1318752 Arhgap33 Rho GTPase activating protein 33 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22810622 1318752 Arhgap33 Rho GTPase activating protein 33 gene MP:0000794 abnormal parietal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:22810622 1318752 Arhgap33 Rho GTPase activating protein 33 gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22810622 1318752 Arhgap33 Rho GTPase activating protein 33 gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22810622 1318752 Arhgap33 Rho GTPase activating protein 33 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1318752 Arhgap33 Rho GTPase activating protein 33 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22810622 1318752 Arhgap33 Rho GTPase activating protein 33 gene MP:0004631 abnormal auditory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22810622 1318752 Arhgap33 Rho GTPase activating protein 33 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22810622 1318752 Arhgap33 Rho GTPase activating protein 33 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22810622 1318752 Arhgap33 Rho GTPase activating protein 33 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22810622 1318752 Arhgap33 Rho GTPase activating protein 33 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1318754 Septin4 septin 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15737930 1318754 Septin4 septin 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15737931 1318754 Septin4 septin 4 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15737931 1318754 Septin4 septin 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15737930 1318754 Septin4 septin 4 gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20141003 MGI PMID:15737931 1318754 Septin4 septin 4 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:15737930 1318754 Septin4 septin 4 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15737931 1318754 Septin4 septin 4 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:15737930 1318754 Septin4 septin 4 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:15737931 1318754 Septin4 septin 4 gene MP:0009242 thin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:15737931 1318754 Septin4 septin 4 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:15737931 1318754 Septin4 septin 4 gene MP:0009835 absent sperm annulus IAGP N RGD:5509061 20141003 MGI PMID:15737930 1318754 Septin4 septin 4 gene MP:0009835 absent sperm annulus IAGP N RGD:5509061 20141003 MGI PMID:15737931 1318754 Septin4 septin 4 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20141003 MGI PMID:15737931 1318754 Septin4 septin 4 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:15737931 1318754 Septin4 septin 4 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220714 MGI PMID:15737931 1318754 Septin4 septin 4 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20180621 MGI PMID:15737930 1318754 Septin4 septin 4 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20180621 MGI PMID:15737931 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:19651815 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210128 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18612384 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:18612384 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:18612384 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0001891 hydrocephaly IEA N RGD:5509061 20210826 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19651815 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:19651815 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210520 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20221215 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20240523 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210520 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:18612384 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0004892 increased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:19651815 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19651815 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20201022 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:19651815 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19651815 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19651815 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0009303 decreased renal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19651815 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210520 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210520 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18612384 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:19651815 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0012134 absent umbilical cord IAGP N RGD:5509061 20141003 MGI PMID:18612384 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0012301 absent umbilical cord blood vessels IAGP N RGD:5509061 20141003 MGI PMID:18612384 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1318757 Tnks tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:19651815 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20170105 MGI 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:24312227 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:24312227 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20151217 MGI PMID:25047565 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:24312227 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20151217 MGI PMID:25047565 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20151217 MGI PMID:25047565 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:24312227 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20151217 MGI PMID:25047565 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20151217 MGI PMID:25047565 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20151217 MGI PMID:25047565 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20151217 MGI PMID:25047565 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20151217 MGI PMID:25047565 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20151217 MGI PMID:25047565 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20151217 MGI PMID:25047565 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20151217 MGI PMID:25047565 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:24312227 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20151217 MGI PMID:25047565 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1318760 Elfn1 leucine rich repeat and fibronectin type III, extracellular 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:25047565 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0000678 abnormal parathyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0003395 abnormal subclavian artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0003955 abnormal ultimobranchial body morphology IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0006339 abnormal third pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0006340 abnormal fourth pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20180614 MGI PMID:25053427 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0010356 abnormal second pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0010395 abnormal pharyngeal arch development IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0010564 abnormal fetal ductus arteriosus morphology IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20141120 MGI PMID:25053427 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0030335 absent third pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0030340 absent fourth pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:21177346 1318762 Ripply3 ripply transcriptional repressor 3 gene MP:0030589 increased pancreatic alpha cell mass IAGP N RGD:5509061 20180614 MGI PMID:25053427 1318764 Jph1 junctophilin 1 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11535622 1318764 Jph1 junctophilin 1 gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:11535622 1318764 Jph1 junctophilin 1 gene MP:0009411 abnormal skeletal muscle fiber triad morphology IAGP N RGD:5509061 20141003 MGI PMID:11535622 1318764 Jph1 junctophilin 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:11535622 1318764 Jph1 junctophilin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11535622 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:20817531 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:15146193 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19491376 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20817531 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19491376 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20817531 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20817531 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:19491376 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15146193 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19491376 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:15146193 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:19491376 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:20817531 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:15146193 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:15146193 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:15146193 1318767 Smc1b structural maintenance of chromosomes 1B gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19491376 1318771 Ddx4 DEAD box helicase 4 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17038506 1318771 Ddx4 DEAD box helicase 4 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23858447 1318771 Ddx4 DEAD box helicase 4 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:10766740 1318771 Ddx4 DEAD box helicase 4 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23858447 1318771 Ddx4 DEAD box helicase 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10766740 1318771 Ddx4 DEAD box helicase 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23858447 1318771 Ddx4 DEAD box helicase 4 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:23858447 1318771 Ddx4 DEAD box helicase 4 gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20141003 MGI PMID:10766740 1318771 Ddx4 DEAD box helicase 4 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:10766740 1318771 Ddx4 DEAD box helicase 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23858447 1318771 Ddx4 DEAD box helicase 4 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17038506 1318771 Ddx4 DEAD box helicase 4 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:10766740 1318771 Ddx4 DEAD box helicase 4 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17038506 1318771 Ddx4 DEAD box helicase 4 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10766740 1318771 Ddx4 DEAD box helicase 4 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20190411 MGI PMID:10766740 1318771 Ddx4 DEAD box helicase 4 gene MP:0030934 decreased primordial germ cell proliferation IAGP N RGD:5509061 20190411 MGI PMID:10766740 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20231207 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0000414 alopecia IAGP N RGD:5509061 20150813 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0000416 sparse hair IAGP N RGD:5509061 20150813 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0000418 focal hair loss IAGP N RGD:5509061 20150813 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20150813 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0000423 delayed hair regrowth IAGP N RGD:5509061 20150813 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20150813 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:18815260 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0001195 flaky skin IAGP N RGD:5509061 20150813 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20150813 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20150813 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:18815260 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0002991 abnormal sebaceous gland physiology IAGP N RGD:5509061 20150813 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0002992 abnormal sebaceous lipid secretion IAGP N RGD:5509061 20150813 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230119 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:18815260 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20150813 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:18815260 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:18815260 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0009794 sebaceous gland hyperplasia IAGP N RGD:5509061 20150813 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0010137 delayed exit from anagen phase IAGP N RGD:5509061 20150813 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0013378 increased sebocyte number IAGP N RGD:5509061 20150813 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0020380 abnormal galactolipid level IAGP N RGD:5509061 20190815 MGI PMID:21491498 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0030571 dilated piliary canal IAGP N RGD:5509061 20180524 MGI PMID:21628453 1318773 Fa2h fatty acid 2-hydroxylase gene MP:0030923 abnormal hair follicle ostium morphology IAGP N RGD:5509061 20181220 MGI PMID:21628453 1318775 Cyp4f39 cytochrome P450, family 4, subfamily f, polypeptide 39 gene MP:0001190 reddish skin IAGP N RGD:5509061 20201015 MGI PMID:31356814 1318775 Cyp4f39 cytochrome P450, family 4, subfamily f, polypeptide 39 gene MP:0001196 shiny skin IAGP N RGD:5509061 20201015 MGI PMID:31356814 1318775 Cyp4f39 cytochrome P450, family 4, subfamily f, polypeptide 39 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20201015 MGI PMID:31356814 1318775 Cyp4f39 cytochrome P450, family 4, subfamily f, polypeptide 39 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20201015 MGI PMID:31356814 1318775 Cyp4f39 cytochrome P450, family 4, subfamily f, polypeptide 39 gene MP:0001263 weight loss IAGP N RGD:5509061 20201015 MGI PMID:31356814 1318775 Cyp4f39 cytochrome P450, family 4, subfamily f, polypeptide 39 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20201015 MGI PMID:31356814 1318775 Cyp4f39 cytochrome P450, family 4, subfamily f, polypeptide 39 gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20201015 MGI PMID:31356814 1318775 Cyp4f39 cytochrome P450, family 4, subfamily f, polypeptide 39 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20201015 MGI PMID:31356814 1318775 Cyp4f39 cytochrome P450, family 4, subfamily f, polypeptide 39 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1318775 Cyp4f39 cytochrome P450, family 4, subfamily f, polypeptide 39 gene MP:0013391 abnormal Meibomian gland physiology IAGP N RGD:5509061 20221117 MGI PMID:34113821 1318775 Cyp4f39 cytochrome P450, family 4, subfamily f, polypeptide 39 gene MP:0013530 abnormal periderm morphology IAGP N RGD:5509061 20201015 MGI PMID:31356814 1318775 Cyp4f39 cytochrome P450, family 4, subfamily f, polypeptide 39 gene MP:0020583 decreased ceramide level IAGP N RGD:5509061 20201015 MGI PMID:31356814 1318775 Cyp4f39 cytochrome P450, family 4, subfamily f, polypeptide 39 gene MP:0030605 abnormal corneocyte morphology IAGP N RGD:5509061 20201015 MGI PMID:31356814 1318776 Ccdc33 coiled-coil domain containing 33 gene MP:0002764 short tibia IEA N RGD:5509061 20160114 MGI 1318778 Gzf1 GDNF-inducible zinc finger protein 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230119 MGI 1318778 Gzf1 GDNF-inducible zinc finger protein 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1318778 Gzf1 GDNF-inducible zinc finger protein 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1318778 Gzf1 GDNF-inducible zinc finger protein 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1318778 Gzf1 GDNF-inducible zinc finger protein 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1318778 Gzf1 GDNF-inducible zinc finger protein 1 gene MP:0002764 short tibia IEA N RGD:5509061 20230119 MGI 1318778 Gzf1 GDNF-inducible zinc finger protein 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20230119 MGI 1318778 Gzf1 GDNF-inducible zinc finger protein 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20240523 MGI 1318778 Gzf1 GDNF-inducible zinc finger protein 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230119 MGI 1318778 Gzf1 GDNF-inducible zinc finger protein 1 gene MP:0004085 abnormal heartbeat IEA N RGD:5509061 20230119 MGI 1318778 Gzf1 GDNF-inducible zinc finger protein 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230119 MGI 1318778 Gzf1 GDNF-inducible zinc finger protein 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20230119 MGI 1318778 Gzf1 GDNF-inducible zinc finger protein 1 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20240523 MGI 1318778 Gzf1 GDNF-inducible zinc finger protein 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1318778 Gzf1 GDNF-inducible zinc finger protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230119 MGI 1318781 Csk c-src tyrosine kinase gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:7685657 1318781 Csk c-src tyrosine kinase gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:9732874 1318781 Csk c-src tyrosine kinase gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:9732874 1318781 Csk c-src tyrosine kinase gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:7685657 1318781 Csk c-src tyrosine kinase gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:7685657 1318781 Csk c-src tyrosine kinase gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:7685657 1318781 Csk c-src tyrosine kinase gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:7685657 1318781 Csk c-src tyrosine kinase gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0001288 abnormal lens induction IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:22348736 1318781 Csk c-src tyrosine kinase gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22348736 1318781 Csk c-src tyrosine kinase gene MP:0001432 abnormal food preference IAGP N RGD:5509061 20141003 MGI PMID:22348736 1318781 Csk c-src tyrosine kinase gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:22348736 1318781 Csk c-src tyrosine kinase gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14975240 1318781 Csk c-src tyrosine kinase gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:7685657 1318781 Csk c-src tyrosine kinase gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20210520 MGI 1318781 Csk c-src tyrosine kinase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1318781 Csk c-src tyrosine kinase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7685657 1318781 Csk c-src tyrosine kinase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20190502 MGI 1318781 Csk c-src tyrosine kinase gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:7685657 1318781 Csk c-src tyrosine kinase gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:7685657 1318781 Csk c-src tyrosine kinase gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20346773 1318781 Csk c-src tyrosine kinase gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20346773 1318781 Csk c-src tyrosine kinase gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:14975240 1318781 Csk c-src tyrosine kinase gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:14975240 1318781 Csk c-src tyrosine kinase gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 1318781 Csk c-src tyrosine kinase gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20190502 MGI 1318781 Csk c-src tyrosine kinase gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1318781 Csk c-src tyrosine kinase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:7685657 1318781 Csk c-src tyrosine kinase gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:7685657 1318781 Csk c-src tyrosine kinase gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:14975240 1318781 Csk c-src tyrosine kinase gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0006293 absent nasal placodes IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9732874 1318781 Csk c-src tyrosine kinase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7685657 1318781 Csk c-src tyrosine kinase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318781 Csk c-src tyrosine kinase gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20141003 MGI PMID:7685657 1318781 Csk c-src tyrosine kinase gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1318781 Csk c-src tyrosine kinase gene MP:0012170 absent optic placodes IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0012707 incomplete caudal neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:8513497 1318781 Csk c-src tyrosine kinase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1318783 Nek11 NIMA (never in mitosis gene a)-related expressed kinase 11 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1318783 Nek11 NIMA (never in mitosis gene a)-related expressed kinase 11 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220519 MGI 1318783 Nek11 NIMA (never in mitosis gene a)-related expressed kinase 11 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1318788 Pgrmc2 progesterone receptor membrane component 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20180315 MGI PMID:28005395 1318788 Pgrmc2 progesterone receptor membrane component 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20180315 MGI PMID:28005395 1318788 Pgrmc2 progesterone receptor membrane component 2 gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20180315 MGI PMID:28005395 1318788 Pgrmc2 progesterone receptor membrane component 2 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20180315 MGI PMID:28005395 1318788 Pgrmc2 progesterone receptor membrane component 2 gene MP:0008876 decreased uterine NK cell number IAGP N RGD:5509061 20180315 MGI PMID:28005395 1318788 Pgrmc2 progesterone receptor membrane component 2 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20180315 MGI PMID:28005395 1318788 Pgrmc2 progesterone receptor membrane component 2 gene MP:0009082 uterus cyst IAGP N RGD:5509061 20180315 MGI PMID:28005395 1318788 Pgrmc2 progesterone receptor membrane component 2 gene MP:0009094 abnormal endometrial gland morphology IAGP N RGD:5509061 20180315 MGI PMID:28005395 1318788 Pgrmc2 progesterone receptor membrane component 2 gene MP:0009251 enlarged endometrial glands IAGP N RGD:5509061 20180315 MGI PMID:28005395 1318788 Pgrmc2 progesterone receptor membrane component 2 gene MP:0013401 increased endometrial gland number IAGP N RGD:5509061 20180315 MGI PMID:28005395 1318792 Mon2 MON2 homolog, regulator of endosome to Golgi trafficking gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1318792 Mon2 MON2 homolog, regulator of endosome to Golgi trafficking gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1318792 Mon2 MON2 homolog, regulator of endosome to Golgi trafficking gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1318792 Mon2 MON2 homolog, regulator of endosome to Golgi trafficking gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318792 Mon2 MON2 homolog, regulator of endosome to Golgi trafficking gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:9808625 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:9808625 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9808625 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0000692 small spleen IAGP N RGD:5509061 20170824 MGI PMID:26443207 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9808625 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0001599 abnormal blood volume IAGP N RGD:5509061 20141003 MGI PMID:9808625 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9808625 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14642567 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9808625 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14642567 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11101838 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16914751 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11101838 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14642567 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:12242442 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12242442 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11101838 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11101838 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12242442 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:9808625 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0002424 abnormal reticulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9808625 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14642567 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9808625 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20170824 MGI PMID:26443207 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:14642567 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0003701 elevated level of mitotic sister chromatid exchange IAGP N RGD:5509061 20170824 MGI PMID:26443207 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:14642567 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9808625 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:12242442 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:23254285 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20170824 MGI PMID:26443207 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170824 MGI PMID:26443207 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12242442 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16914751 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14642567 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9808625 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11101838 1318796 Blm Bloom syndrome, RecQ like helicase gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14642567 1318802 Mkks McKusick-Kaufman syndrome gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16170314 1318802 Mkks McKusick-Kaufman syndrome gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15772095 1318802 Mkks McKusick-Kaufman syndrome gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15772095 1318802 Mkks McKusick-Kaufman syndrome gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:16170314 1318802 Mkks McKusick-Kaufman syndrome gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15772095 1318802 Mkks McKusick-Kaufman syndrome gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15772095 1318802 Mkks McKusick-Kaufman syndrome gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:15772095 1318802 Mkks McKusick-Kaufman syndrome gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15772095 1318802 Mkks McKusick-Kaufman syndrome gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16170314 1318802 Mkks McKusick-Kaufman syndrome gene MP:0004512 anosmia IAGP N RGD:5509061 20141003 MGI PMID:16170314 1318802 Mkks McKusick-Kaufman syndrome gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:16170314 1318802 Mkks McKusick-Kaufman syndrome gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:16170314 1318802 Mkks McKusick-Kaufman syndrome gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:15772095 1318802 Mkks McKusick-Kaufman syndrome gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15772095 1318802 Mkks McKusick-Kaufman syndrome gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:18032602 1318802 Mkks McKusick-Kaufman syndrome gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:16170314 1318802 Mkks McKusick-Kaufman syndrome gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:18032602 1318802 Mkks McKusick-Kaufman syndrome gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:18032602 1318802 Mkks McKusick-Kaufman syndrome gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:18032602 1318802 Mkks McKusick-Kaufman syndrome gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:15772095 1318802 Mkks McKusick-Kaufman syndrome gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16170314 1318802 Mkks McKusick-Kaufman syndrome gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16170314 1318802 Mkks McKusick-Kaufman syndrome gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15772095 1318802 Mkks McKusick-Kaufman syndrome gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:18032602 1318802 Mkks McKusick-Kaufman syndrome gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:15772095 1318802 Mkks McKusick-Kaufman syndrome gene MP:0030962 abnormal inner hair cell kinocilium location or orientation IAGP N RGD:5509061 20190725 MGI PMID:16170314 1318802 Mkks McKusick-Kaufman syndrome gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:15772095 1318802 Mkks McKusick-Kaufman syndrome gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:16170314 1318804 Alg6 ALG6 alpha-1,3-glucosyltransferase gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20190502 MGI 1318804 Alg6 ALG6 alpha-1,3-glucosyltransferase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1318804 Alg6 ALG6 alpha-1,3-glucosyltransferase gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20210520 MGI 1318804 Alg6 ALG6 alpha-1,3-glucosyltransferase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1318804 Alg6 ALG6 alpha-1,3-glucosyltransferase gene MP:0001726 abnormal allantois morphology IEA N RGD:5509061 20190502 MGI 1318804 Alg6 ALG6 alpha-1,3-glucosyltransferase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20190502 MGI 1318804 Alg6 ALG6 alpha-1,3-glucosyltransferase gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IEA N RGD:5509061 20220519 MGI 1318804 Alg6 ALG6 alpha-1,3-glucosyltransferase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1318804 Alg6 ALG6 alpha-1,3-glucosyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1318804 Alg6 ALG6 alpha-1,3-glucosyltransferase gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20190502 MGI 1318804 Alg6 ALG6 alpha-1,3-glucosyltransferase gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1318805 Cnep1r1 CTD nuclear envelope phosphatase 1 regulatory subunit 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220811 MGI 1318805 Cnep1r1 CTD nuclear envelope phosphatase 1 regulatory subunit 1 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20210128 MGI 1318805 Cnep1r1 CTD nuclear envelope phosphatase 1 regulatory subunit 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220811 MGI 1318805 Cnep1r1 CTD nuclear envelope phosphatase 1 regulatory subunit 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1318805 Cnep1r1 CTD nuclear envelope phosphatase 1 regulatory subunit 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1318805 Cnep1r1 CTD nuclear envelope phosphatase 1 regulatory subunit 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1318810 Brat1 BRCA1-associated ATM activator 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 1318810 Brat1 BRCA1-associated ATM activator 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1318810 Brat1 BRCA1-associated ATM activator 1 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20230601 MGI 1318810 Brat1 BRCA1-associated ATM activator 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1318820 Psmc6 proteasome (prosome, macropain) 26S subunit, ATPase, 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1318820 Psmc6 proteasome (prosome, macropain) 26S subunit, ATPase, 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318820 Psmc6 proteasome (prosome, macropain) 26S subunit, ATPase, 6 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1318820 Psmc6 proteasome (prosome, macropain) 26S subunit, ATPase, 6 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210520 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160421 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20201022 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20181227 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20160421 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20170105 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20170105 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20221215 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20161201 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:21307874 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20141003 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20160421 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20160421 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20170105 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20160811 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20141003 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20141003 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0002544 brachydactyly IEA N RGD:5509061 20160421 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0002764 short tibia IEA N RGD:5509061 20160421 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20141003 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:21307874 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:23870131 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160421 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:21307874 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20211021 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20221215 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20221215 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20160421 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20221215 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20221215 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20240523 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20160421 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23870131 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0011952 decreased cardiac stroke volume IEA N RGD:5509061 20210128 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0011999 abnormal tail length IEA N RGD:5509061 20201022 MGI 1318822 Dnase1l2 deoxyribonuclease 1-like 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1318824 Sephs2 selenophosphate synthetase 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1318824 Sephs2 selenophosphate synthetase 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1318824 Sephs2 selenophosphate synthetase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1318824 Sephs2 selenophosphate synthetase 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1318827 Gcdh glutaryl-Coenzyme A dehydrogenase gene MP:0001263 weight loss IAGP N RGD:5509061 20190103 MGI PMID:28545977 1318827 Gcdh glutaryl-Coenzyme A dehydrogenase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190103 MGI PMID:28545977 1318827 Gcdh glutaryl-Coenzyme A dehydrogenase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11854167 1318827 Gcdh glutaryl-Coenzyme A dehydrogenase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190103 MGI PMID:28545977 1318827 Gcdh glutaryl-Coenzyme A dehydrogenase gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:11854167 1318827 Gcdh glutaryl-Coenzyme A dehydrogenase gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:11854167 1318827 Gcdh glutaryl-Coenzyme A dehydrogenase gene MP:0002931 glutaricadicuria IAGP N RGD:5509061 20141003 MGI PMID:11854167 1318827 Gcdh glutaryl-Coenzyme A dehydrogenase gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:11854167 1318827 Gcdh glutaryl-Coenzyme A dehydrogenase gene MP:0005202 lethargy IAGP N RGD:5509061 20190103 MGI PMID:28545977 1318827 Gcdh glutaryl-Coenzyme A dehydrogenase gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20220519 MGI 1318827 Gcdh glutaryl-Coenzyme A dehydrogenase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1318827 Gcdh glutaryl-Coenzyme A dehydrogenase gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20190103 MGI PMID:28545977 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0002175 decreased brain weight IEA N RGD:5509061 20220519 MGI 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0005451 abnormal body composition IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0009130 increased white fat cell number IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318830 Creb3 cAMP responsive element binding protein 3 gene MP:0031414 decreased skeletal muscle triglyceride level IAGP N RGD:5509061 20240328 MGI PMID:35637262 1318832 Mbd3l2 methyl-CpG binding domain protein 3-like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18942147 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23095888 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20170209 MGI 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20170209 MGI 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0002639 micrognathia IEA N RGD:5509061 20170209 MGI 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0004407 increased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0006198 enophthalmos IEA N RGD:5509061 20170209 MGI 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0006286 inner ear hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23095888 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0011666 double outlet right ventricle, ventricular defect committed to aorta IEA N RGD:5509061 20170209 MGI 1318834 Dvl3 dishevelled segment polarity protein 3 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:19008950 1318840 Cldn6 claudin 6 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:22900086 1318840 Cldn6 claudin 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22900086 1318840 Cldn6 claudin 6 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:22900086 1318840 Cldn6 claudin 6 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1318840 Cldn6 claudin 6 gene MP:0002861 abnormal tail bud morphology IAGP N RGD:5509061 20141003 MGI PMID:22900086 1318840 Cldn6 claudin 6 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:22900086 1318840 Cldn6 claudin 6 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:22900086 1318840 Cldn6 claudin 6 gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:22900086 1318840 Cldn6 claudin 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22900086 1318840 Cldn6 claudin 6 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22900086 1318840 Cldn6 claudin 6 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22900086 1318842 Krt23 keratin 23 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1318844 Tmeff2 transmembrane protein with EGF-like and two follistatin-like domains 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22828515 1318844 Tmeff2 transmembrane protein with EGF-like and two follistatin-like domains 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1318844 Tmeff2 transmembrane protein with EGF-like and two follistatin-like domains 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22828515 1318844 Tmeff2 transmembrane protein with EGF-like and two follistatin-like domains 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1318844 Tmeff2 transmembrane protein with EGF-like and two follistatin-like domains 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1318844 Tmeff2 transmembrane protein with EGF-like and two follistatin-like domains 2 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20240523 MGI 1318844 Tmeff2 transmembrane protein with EGF-like and two follistatin-like domains 2 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20240523 MGI 1318844 Tmeff2 transmembrane protein with EGF-like and two follistatin-like domains 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:22828515 1318844 Tmeff2 transmembrane protein with EGF-like and two follistatin-like domains 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1318844 Tmeff2 transmembrane protein with EGF-like and two follistatin-like domains 2 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22828515 1318844 Tmeff2 transmembrane protein with EGF-like and two follistatin-like domains 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 1318846 Man2b2 mannosidase 2, alpha B2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1318846 Man2b2 mannosidase 2, alpha B2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20160811 MGI 1318846 Man2b2 mannosidase 2, alpha B2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 1318846 Man2b2 mannosidase 2, alpha B2 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20160811 MGI 1318846 Man2b2 mannosidase 2, alpha B2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1318846 Man2b2 mannosidase 2, alpha B2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1318846 Man2b2 mannosidase 2, alpha B2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1318846 Man2b2 mannosidase 2, alpha B2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 1318846 Man2b2 mannosidase 2, alpha B2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20201022 MGI 1318846 Man2b2 mannosidase 2, alpha B2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11747814 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:23213437 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20691046 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11747814 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:23213437 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11747814 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20691046 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:23213437 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:23213437 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:20691046 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:11747814 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:20691046 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:20691046 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0004273 abnormal basal lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:11747814 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0004360 absent ulna IAGP N RGD:5509061 20141003 MGI PMID:23213437 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:20691046 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20691046 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:23213437 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11747814 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:23213437 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:20691046 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20691046 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11747814 1318852 Reck reversion-inducing-cysteine-rich protein with kazal motifs gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20691046 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15809356 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:15809356 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:15809356 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12150927 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:12150927 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:12150927 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15809356 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:15809356 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20161027 MGI PMID:24696448 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12150927 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20161027 MGI PMID:24696448 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20161027 MGI PMID:24696448 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:12150927 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20161027 MGI PMID:24696448 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0002869 increased anti-insulin autoantibody level IAGP N RGD:5509061 20161027 MGI PMID:24696448 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15809356 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0004031 insulitis IAGP N RGD:5509061 20161027 MGI PMID:24696448 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20161027 MGI PMID:24696448 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:15809356 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:15809356 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20161027 MGI PMID:24696448 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0008136 enlarged Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12150927 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:15809356 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:12150927 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:12150927 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:12150927 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12150927 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:15809356 1318854 Irak3 interleukin-1 receptor-associated kinase 3 gene MP:0013772 increased effector memory T-helper cell number IAGP N RGD:5509061 20161027 MGI PMID:24696448 1318856 Ogfod1 2-oxoglutarate and iron-dependent oxygenase domain containing 1 gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20160804 MGI 1318856 Ogfod1 2-oxoglutarate and iron-dependent oxygenase domain containing 1 gene MP:0001191 abnormal skin condition IEA N RGD:5509061 20160804 MGI 1318856 Ogfod1 2-oxoglutarate and iron-dependent oxygenase domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150101 MGI PMID:24550447 1318856 Ogfod1 2-oxoglutarate and iron-dependent oxygenase domain containing 1 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20160804 MGI 1318858 Rdh5 retinol dehydrogenase 5 gene MP:0003011 delayed dark adaptation IAGP N RGD:5509061 20141003 MGI PMID:11907141 1318858 Rdh5 retinol dehydrogenase 5 gene MP:0003011 delayed dark adaptation IAGP N RGD:5509061 20141003 MGI PMID:15634683 1318858 Rdh5 retinol dehydrogenase 5 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11907141 1318858 Rdh5 retinol dehydrogenase 5 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15634683 1318859 Tmem72 transmembrane protein 72 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1318859 Tmem72 transmembrane protein 72 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20190808 MGI 1318859 Tmem72 transmembrane protein 72 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1318859 Tmem72 transmembrane protein 72 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210826 MGI 1318859 Tmem72 transmembrane protein 72 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20190808 MGI 1318859 Tmem72 transmembrane protein 72 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1318859 Tmem72 transmembrane protein 72 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20190808 MGI 1318859 Tmem72 transmembrane protein 72 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 1318859 Tmem72 transmembrane protein 72 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210826 MGI 1318859 Tmem72 transmembrane protein 72 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20190808 MGI 1318859 Tmem72 transmembrane protein 72 gene MP:0010052 increased grip strength IEA N RGD:5509061 20200402 MGI 1318861 Grhpr glyoxylate reductase/hydroxypyruvate reductase gene MP:0002708 nephrolithiasis IAGP N RGD:5509061 20141003 MGI PMID:22189945 1318861 Grhpr glyoxylate reductase/hydroxypyruvate reductase gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:22189945 1318861 Grhpr glyoxylate reductase/hydroxypyruvate reductase gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22189945 1318861 Grhpr glyoxylate reductase/hydroxypyruvate reductase gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:22189945 1318861 Grhpr glyoxylate reductase/hydroxypyruvate reductase gene MP:0005360 urolithiasis IAGP N RGD:5509061 20141003 MGI PMID:22189945 1318861 Grhpr glyoxylate reductase/hydroxypyruvate reductase gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22189945 1318861 Grhpr glyoxylate reductase/hydroxypyruvate reductase gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20201210 MGI PMID:31821850 1318861 Grhpr glyoxylate reductase/hydroxypyruvate reductase gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20201210 MGI PMID:31821850 1318861 Grhpr glyoxylate reductase/hydroxypyruvate reductase gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22189945 1318861 Grhpr glyoxylate reductase/hydroxypyruvate reductase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22189945 1318861 Grhpr glyoxylate reductase/hydroxypyruvate reductase gene MP:0009646 urinary bladder inflammation IAGP N RGD:5509061 20141003 MGI PMID:22189945 1318861 Grhpr glyoxylate reductase/hydroxypyruvate reductase gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:22189945 1318861 Grhpr glyoxylate reductase/hydroxypyruvate reductase gene MP:0011517 hyperoxaluria IAGP N RGD:5509061 20141003 MGI PMID:22189945 1318861 Grhpr glyoxylate reductase/hydroxypyruvate reductase gene MP:0011517 hyperoxaluria IAGP N RGD:5509061 20201210 MGI PMID:31821850 1318863 Usp3 ubiquitin specific peptidase 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1318870 Rnf144b ring finger protein 144B gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20160421 MGI 1318870 Rnf144b ring finger protein 144B gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20160421 MGI 1318870 Rnf144b ring finger protein 144B gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1318875 Blk B lymphoid kinase gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20160811 MGI 1318875 Blk B lymphoid kinase gene MP:0001147 small testis IEA N RGD:5509061 20160811 MGI 1318875 Blk B lymphoid kinase gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12563261 1318875 Blk B lymphoid kinase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12563261 1318875 Blk B lymphoid kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10648608 1318875 Blk B lymphoid kinase gene MP:0002497 increased IgE level IEA N RGD:5509061 20180215 MGI 1318875 Blk B lymphoid kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563261 1318875 Blk B lymphoid kinase gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563261 1318875 Blk B lymphoid kinase gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563261 1318875 Blk B lymphoid kinase gene MP:0008233 abnormal pro-B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12563261 1318875 Blk B lymphoid kinase gene MP:0008657 increased interleukin-1 beta secretion IEA N RGD:5509061 20180215 MGI 1318879 Sec62 SEC62 homolog, preprotein translocation gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1318879 Sec62 SEC62 homolog, preprotein translocation gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1318879 Sec62 SEC62 homolog, preprotein translocation gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1318879 Sec62 SEC62 homolog, preprotein translocation gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1318883 Fus fused in sarcoma gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:10655065 1318883 Fus fused in sarcoma gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20171228 MGI PMID:29053787 1318883 Fus fused in sarcoma gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20171228 MGI PMID:29053787 1318883 Fus fused in sarcoma gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20170223 MGI PMID:26842965 1318883 Fus fused in sarcoma gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20171228 MGI PMID:29053787 1318883 Fus fused in sarcoma gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:10654943 1318883 Fus fused in sarcoma gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10654943 1318883 Fus fused in sarcoma gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10654943 1318883 Fus fused in sarcoma gene MP:0001406 abnormal gait IAGP N RGD:5509061 20171228 MGI PMID:29053787 1318883 Fus fused in sarcoma gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:10655065 1318883 Fus fused in sarcoma gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20171228 MGI PMID:29053787 1318883 Fus fused in sarcoma gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:10654943 1318883 Fus fused in sarcoma gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1318883 Fus fused in sarcoma gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10654943 1318883 Fus fused in sarcoma gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10654943 1318883 Fus fused in sarcoma gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10654943 1318883 Fus fused in sarcoma gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10654943 1318883 Fus fused in sarcoma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10654943 1318883 Fus fused in sarcoma gene MP:0002083 premature death IAGP N RGD:5509061 20171228 MGI PMID:29053787 1318883 Fus fused in sarcoma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170223 MGI PMID:26842965 1318883 Fus fused in sarcoma gene MP:0002223 lymphoid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10655065 1318883 Fus fused in sarcoma gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:10655065 1318883 Fus fused in sarcoma gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:10655065 1318883 Fus fused in sarcoma gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:10655065 1318883 Fus fused in sarcoma gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:10655065 1318883 Fus fused in sarcoma gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10655065 1318883 Fus fused in sarcoma gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10655065 1318883 Fus fused in sarcoma gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:10654943 1318883 Fus fused in sarcoma gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20160421 MGI 1318883 Fus fused in sarcoma gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15797031 1318883 Fus fused in sarcoma gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20210128 MGI 1318883 Fus fused in sarcoma gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10654943 1318883 Fus fused in sarcoma gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10655065 1318883 Fus fused in sarcoma gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170223 MGI PMID:26842965 1318883 Fus fused in sarcoma gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1318885 Gpatch2 G patch domain containing 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20230817 MGI PMID:36973252 1318887 Map7 microtubule-associated protein 7 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:10837026 1318887 Map7 microtubule-associated protein 7 gene MP:0001147 small testis IAGP N RGD:5509061 20150122 MGI PMID:19329343 1318887 Map7 microtubule-associated protein 7 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:10837026 1318887 Map7 microtubule-associated protein 7 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:8875885 1318887 Map7 microtubule-associated protein 7 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:10837026 1318887 Map7 microtubule-associated protein 7 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20150122 MGI PMID:19329343 1318887 Map7 microtubule-associated protein 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10837026 1318887 Map7 microtubule-associated protein 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8875885 1318887 Map7 microtubule-associated protein 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20150122 MGI PMID:19329343 1318887 Map7 microtubule-associated protein 7 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10837026 1318887 Map7 microtubule-associated protein 7 gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10837026 1318887 Map7 microtubule-associated protein 7 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:8875885 1318887 Map7 microtubule-associated protein 7 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20150122 MGI PMID:19329343 1318887 Map7 microtubule-associated protein 7 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10837026 1318887 Map7 microtubule-associated protein 7 gene MP:0004752 decreased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:8875885 1318887 Map7 microtubule-associated protein 7 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20150122 MGI PMID:19329343 1318887 Map7 microtubule-associated protein 7 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20150122 MGI PMID:19329343 1318887 Map7 microtubule-associated protein 7 gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:10837026 1318887 Map7 microtubule-associated protein 7 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:10837026 1318887 Map7 microtubule-associated protein 7 gene MP:0006428 ectopic Sertoli cells IAGP N RGD:5509061 20160915 MGI PMID:8875885 1318887 Map7 microtubule-associated protein 7 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:8875885 1318887 Map7 microtubule-associated protein 7 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8875885 1318889 Arpc5l actin related protein 2/3 complex, subunit 5-like gene MP:0001406 abnormal gait IEA N RGD:5509061 20201022 MGI 1318889 Arpc5l actin related protein 2/3 complex, subunit 5-like gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1318889 Arpc5l actin related protein 2/3 complex, subunit 5-like gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1318889 Arpc5l actin related protein 2/3 complex, subunit 5-like gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0000452 abnormal mouth morphology IEA N RGD:5509061 20210128 MGI 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20210826 MGI 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20230601 MGI 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20200402 MGI 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20191114 MGI PMID:28559441 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20200402 MGI 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20191114 MGI PMID:28559441 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20191114 MGI PMID:30704515 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220519 MGI 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0004222 iris synechia IEA N RGD:5509061 20200402 MGI 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20191114 MGI PMID:28559441 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20191114 MGI PMID:28559441 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20191114 MGI PMID:28559441 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20191114 MGI PMID:28559441 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20191114 MGI PMID:28559441 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20191114 MGI PMID:30704515 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0009130 increased white fat cell number IAGP N RGD:5509061 20191114 MGI PMID:28559441 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20191114 MGI PMID:28559441 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220519 MGI 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20191114 MGI PMID:28559441 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0011939 increased food intake IAGP N RGD:5509061 20191114 MGI PMID:28559441 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0013258 abnormal extracellular matrix morphology IAGP N RGD:5509061 20191114 MGI PMID:28559441 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20191114 MGI PMID:28559441 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20191114 MGI PMID:28559441 1318898 Apmap adipocyte plasma membrane associated protein gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20191114 MGI PMID:28559441 1318901 Trmt6 tRNA methyltransferase 6 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:36138184 1318901 Trmt6 tRNA methyltransferase 6 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20231109 MGI PMID:36138184 1318903 Amdhd1 amidohydrolase domain containing 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20210826 MGI 1318907 Sult2b1 sulfotransferase family, cytosolic, 2B, member 1 gene MP:0003947 abnormal cholesterol level IEA N RGD:5509061 20141003 MGI 1318910 Mcoln2 mucolipin 2 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20170803 MGI PMID:26432893 1318910 Mcoln2 mucolipin 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20170803 MGI PMID:26432893 1318910 Mcoln2 mucolipin 2 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20170803 MGI PMID:26432893 1318910 Mcoln2 mucolipin 2 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20170803 MGI PMID:26432893 1318910 Mcoln2 mucolipin 2 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20170803 MGI PMID:26432893 1318912 Trim41 tripartite motif-containing 41 gene MP:0001147 small testis IAGP N RGD:5509061 20240912 MGI PMID:35648791 1318912 Trim41 tripartite motif-containing 41 gene MP:0001925 male infertility IAGP N RGD:5509061 20240912 MGI PMID:35648791 1318912 Trim41 tripartite motif-containing 41 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20240829 MGI PMID:33640899 1318912 Trim41 tripartite motif-containing 41 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20240829 MGI PMID:33640899 1318912 Trim41 tripartite motif-containing 41 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240912 MGI PMID:35648791 1318912 Trim41 tripartite motif-containing 41 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240912 MGI PMID:35648791 1318912 Trim41 tripartite motif-containing 41 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20240912 MGI PMID:35648791 1318912 Trim41 tripartite motif-containing 41 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20240912 MGI PMID:35648791 1318912 Trim41 tripartite motif-containing 41 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20240829 MGI PMID:33640899 1318912 Trim41 tripartite motif-containing 41 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20240829 MGI PMID:33640899 1318912 Trim41 tripartite motif-containing 41 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20240829 MGI PMID:33640899 1318912 Trim41 tripartite motif-containing 41 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20240912 MGI PMID:35648791 1318912 Trim41 tripartite motif-containing 41 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240912 MGI PMID:35648791 1318912 Trim41 tripartite motif-containing 41 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20240912 MGI PMID:35648791 1318912 Trim41 tripartite motif-containing 41 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20240829 MGI PMID:33640899 1318912 Trim41 tripartite motif-containing 41 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20240912 MGI PMID:35648791 1318912 Trim41 tripartite motif-containing 41 gene MP:0014436 decreased interferon level IAGP N RGD:5509061 20240829 MGI PMID:33640899 1318912 Trim41 tripartite motif-containing 41 gene MP:0014438 decreased interleukin level IAGP N RGD:5509061 20240829 MGI PMID:33640899 1318912 Trim41 tripartite motif-containing 41 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20240829 MGI PMID:33640899 1318912 Trim41 tripartite motif-containing 41 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20240829 MGI PMID:33640899 1318912 Trim41 tripartite motif-containing 41 gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20240829 MGI PMID:33640899 1318912 Trim41 tripartite motif-containing 41 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20240829 MGI PMID:33640899 1318917 Dhx30 DExH-box helicase 30 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1318917 Dhx30 DExH-box helicase 30 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1318917 Dhx30 DExH-box helicase 30 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20211021 MGI 1318917 Dhx30 DExH-box helicase 30 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20160225 MGI PMID:25219788 1318917 Dhx30 DExH-box helicase 30 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160225 MGI PMID:25219788 1318917 Dhx30 DExH-box helicase 30 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20160225 MGI PMID:25219788 1318917 Dhx30 DExH-box helicase 30 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20181227 MGI 1318917 Dhx30 DExH-box helicase 30 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1318917 Dhx30 DExH-box helicase 30 gene MP:0006386 absent somites IAGP N RGD:5509061 20160225 MGI PMID:25219788 1318917 Dhx30 DExH-box helicase 30 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160225 MGI PMID:25219788 1318917 Dhx30 DExH-box helicase 30 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318917 Dhx30 DExH-box helicase 30 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 1318917 Dhx30 DExH-box helicase 30 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1318919 Lama2 laminin, alpha 2 gene MP:0000032 cochlear degeneration IAGP N RGD:5509061 20141003 MGI PMID:12126936 1318919 Lama2 laminin, alpha 2 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:12126936 1318919 Lama2 laminin, alpha 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:12126936 1318919 Lama2 laminin, alpha 2 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16589799 1318919 Lama2 laminin, alpha 2 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:12044978 1318919 Lama2 laminin, alpha 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17459142 1318919 Lama2 laminin, alpha 2 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20141003 MGI PMID:17459142 1318919 Lama2 laminin, alpha 2 gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10792494 1318919 Lama2 laminin, alpha 2 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:9326364 1318919 Lama2 laminin, alpha 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15699217 1318919 Lama2 laminin, alpha 2 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:12044978 1318919 Lama2 laminin, alpha 2 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:12126936 1318919 Lama2 laminin, alpha 2 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:20876525 1318919 Lama2 laminin, alpha 2 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:16589799 1318919 Lama2 laminin, alpha 2 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:20876525 1318919 Lama2 laminin, alpha 2 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:18430779 1318919 Lama2 laminin, alpha 2 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:9326364 1318919 Lama2 laminin, alpha 2 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:10616210 1318919 Lama2 laminin, alpha 2 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:12044978 1318919 Lama2 laminin, alpha 2 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:16589799 1318919 Lama2 laminin, alpha 2 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:18430779 1318919 Lama2 laminin, alpha 2 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:20876525 1318919 Lama2 laminin, alpha 2 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:5434356 1318919 Lama2 laminin, alpha 2 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:9326364 1318919 Lama2 laminin, alpha 2 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:9710454 1318919 Lama2 laminin, alpha 2 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:16589799 1318919 Lama2 laminin, alpha 2 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:20876525 1318919 Lama2 laminin, alpha 2 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:5434356 1318919 Lama2 laminin, alpha 2 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:9710454 1318919 Lama2 laminin, alpha 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12044978 1318919 Lama2 laminin, alpha 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9326364 1318919 Lama2 laminin, alpha 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15699217 1318919 Lama2 laminin, alpha 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:18430779 1318919 Lama2 laminin, alpha 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:4120487 1318919 Lama2 laminin, alpha 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:6831246 1318919 Lama2 laminin, alpha 2 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:6831246 1318919 Lama2 laminin, alpha 2 gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:15699217 1318919 Lama2 laminin, alpha 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:16127160 1318919 Lama2 laminin, alpha 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12044978 1318919 Lama2 laminin, alpha 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:1301630 1318919 Lama2 laminin, alpha 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15578095 1318919 Lama2 laminin, alpha 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16589799 1318919 Lama2 laminin, alpha 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18430779 1318919 Lama2 laminin, alpha 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:2989438 1318919 Lama2 laminin, alpha 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9710454 1318919 Lama2 laminin, alpha 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15578095 1318919 Lama2 laminin, alpha 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15699217 1318919 Lama2 laminin, alpha 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20876525 1318919 Lama2 laminin, alpha 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9326364 1318919 Lama2 laminin, alpha 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9710454 1318919 Lama2 laminin, alpha 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16589799 1318919 Lama2 laminin, alpha 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9326364 1318919 Lama2 laminin, alpha 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:15823249 1318919 Lama2 laminin, alpha 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15699217 1318919 Lama2 laminin, alpha 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:5434356 1318919 Lama2 laminin, alpha 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:9710454 1318919 Lama2 laminin, alpha 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:1301630 1318919 Lama2 laminin, alpha 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:2989438 1318919 Lama2 laminin, alpha 2 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:12044978 1318919 Lama2 laminin, alpha 2 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:15578095 1318919 Lama2 laminin, alpha 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12044978 1318919 Lama2 laminin, alpha 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9326364 1318919 Lama2 laminin, alpha 2 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12044978 1318919 Lama2 laminin, alpha 2 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12126936 1318919 Lama2 laminin, alpha 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:15699217 1318919 Lama2 laminin, alpha 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12044978 1318919 Lama2 laminin, alpha 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16589799 1318919 Lama2 laminin, alpha 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20876525 1318919 Lama2 laminin, alpha 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9326364 1318919 Lama2 laminin, alpha 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9710454 1318919 Lama2 laminin, alpha 2 gene MP:0002083 premature death IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0002083 premature death IAGP N RGD:5509061 20201015 MGI PMID:32017711 1318919 Lama2 laminin, alpha 2 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:15578095 1318919 Lama2 laminin, alpha 2 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:12044978 1318919 Lama2 laminin, alpha 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:2989438 1318919 Lama2 laminin, alpha 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16127160 1318919 Lama2 laminin, alpha 2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12044978 1318919 Lama2 laminin, alpha 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12044978 1318919 Lama2 laminin, alpha 2 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:16589799 1318919 Lama2 laminin, alpha 2 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12126936 1318919 Lama2 laminin, alpha 2 gene MP:0002880 opisthotonus IAGP N RGD:5509061 20141003 MGI PMID:5434356 1318919 Lama2 laminin, alpha 2 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:15823249 1318919 Lama2 laminin, alpha 2 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15578095 1318919 Lama2 laminin, alpha 2 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16589799 1318919 Lama2 laminin, alpha 2 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:3440862 1318919 Lama2 laminin, alpha 2 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9326364 1318919 Lama2 laminin, alpha 2 gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:10792494 1318919 Lama2 laminin, alpha 2 gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12044978 1318919 Lama2 laminin, alpha 2 gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18430779 1318919 Lama2 laminin, alpha 2 gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:3440862 1318919 Lama2 laminin, alpha 2 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:2989438 1318919 Lama2 laminin, alpha 2 gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:16589799 1318919 Lama2 laminin, alpha 2 gene MP:0004262 abnormal physical strength IAGP N RGD:5509061 20141003 MGI PMID:12044978 1318919 Lama2 laminin, alpha 2 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:1161034 1318919 Lama2 laminin, alpha 2 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16127160 1318919 Lama2 laminin, alpha 2 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:894325 1318919 Lama2 laminin, alpha 2 gene MP:0004273 abnormal basal lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:15699217 1318919 Lama2 laminin, alpha 2 gene MP:0004273 abnormal basal lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:18430779 1318919 Lama2 laminin, alpha 2 gene MP:0004273 abnormal basal lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:9326364 1318919 Lama2 laminin, alpha 2 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:17344408 1318919 Lama2 laminin, alpha 2 gene MP:0004289 abnormal bony labyrinth IAGP N RGD:5509061 20141003 MGI PMID:12126936 1318919 Lama2 laminin, alpha 2 gene MP:0004300 abnormal organ of Corti supporting cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12126936 1318919 Lama2 laminin, alpha 2 gene MP:0004325 absent vestibular hair cells IAGP N RGD:5509061 20141003 MGI PMID:12126936 1318919 Lama2 laminin, alpha 2 gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20141003 MGI PMID:12126936 1318919 Lama2 laminin, alpha 2 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:12126936 1318919 Lama2 laminin, alpha 2 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:20876525 1318919 Lama2 laminin, alpha 2 gene MP:0004716 abnormal cochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12126936 1318919 Lama2 laminin, alpha 2 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:61889 1318919 Lama2 laminin, alpha 2 gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:15578095 1318919 Lama2 laminin, alpha 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:1301630 1318919 Lama2 laminin, alpha 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10792494 1318919 Lama2 laminin, alpha 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10792494 1318919 Lama2 laminin, alpha 2 gene MP:0005124 increased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:1301630 1318919 Lama2 laminin, alpha 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:16589799 1318919 Lama2 laminin, alpha 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0005426 tachypnea IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:9710454 1318919 Lama2 laminin, alpha 2 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20201015 MGI PMID:32017711 1318919 Lama2 laminin, alpha 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:16127160 1318919 Lama2 laminin, alpha 2 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:630405 1318919 Lama2 laminin, alpha 2 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:16589799 1318919 Lama2 laminin, alpha 2 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:18430779 1318919 Lama2 laminin, alpha 2 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:3440862 1318919 Lama2 laminin, alpha 2 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:9326364 1318919 Lama2 laminin, alpha 2 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:16589799 1318919 Lama2 laminin, alpha 2 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:3440862 1318919 Lama2 laminin, alpha 2 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:3440862 1318919 Lama2 laminin, alpha 2 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:3440862 1318919 Lama2 laminin, alpha 2 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0009420 skeletal muscle endomysial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18430779 1318919 Lama2 laminin, alpha 2 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:10792494 1318919 Lama2 laminin, alpha 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20201015 MGI PMID:32017711 1318919 Lama2 laminin, alpha 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15699217 1318919 Lama2 laminin, alpha 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9710454 1318919 Lama2 laminin, alpha 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20876525 1318919 Lama2 laminin, alpha 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12126936 1318919 Lama2 laminin, alpha 2 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:10616210 1318919 Lama2 laminin, alpha 2 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:15578095 1318919 Lama2 laminin, alpha 2 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:18430779 1318919 Lama2 laminin, alpha 2 gene MP:0020380 abnormal galactolipid level IAGP N RGD:5509061 20190815 MGI PMID:2989438 1318919 Lama2 laminin, alpha 2 gene MP:0020452 abnormal axon radial sorting IAGP N RGD:5509061 20170914 MGI PMID:15699217 1318919 Lama2 laminin, alpha 2 gene MP:0030798 joint contracture IAGP N RGD:5509061 20181122 MGI PMID:12609503 1318919 Lama2 laminin, alpha 2 gene MP:0030979 decreased spinal cord weight IAGP N RGD:5509061 20191010 MGI PMID:2989438 1318919 Lama2 laminin, alpha 2 gene MP:0031204 hindlimb paresis IAGP N RGD:5509061 20210218 MGI PMID:18430779 1318919 Lama2 laminin, alpha 2 gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:18430779 1318924 Dcun1d3 defective in cullin neddylation 1 domain containing 3 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1318924 Dcun1d3 defective in cullin neddylation 1 domain containing 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1318924 Dcun1d3 defective in cullin neddylation 1 domain containing 3 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20231207 MGI 1318924 Dcun1d3 defective in cullin neddylation 1 domain containing 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1318924 Dcun1d3 defective in cullin neddylation 1 domain containing 3 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1318924 Dcun1d3 defective in cullin neddylation 1 domain containing 3 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 1318924 Dcun1d3 defective in cullin neddylation 1 domain containing 3 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1318924 Dcun1d3 defective in cullin neddylation 1 domain containing 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20181227 MGI 1318924 Dcun1d3 defective in cullin neddylation 1 domain containing 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20211021 MGI 1318924 Dcun1d3 defective in cullin neddylation 1 domain containing 3 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1318924 Dcun1d3 defective in cullin neddylation 1 domain containing 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1318924 Dcun1d3 defective in cullin neddylation 1 domain containing 3 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:7506762 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:939913 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19797173 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:939913 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:939913 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:19017726 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:939913 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20160114 MGI PMID:25198651 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:7506762 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:939913 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:647395 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:7472477 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:7506762 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:647395 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7472477 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001108 absent Schwann cells IAGP N RGD:5509061 20141003 MGI PMID:647395 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:939913 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7506762 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7602333 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:7602333 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:939913 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:7506762 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:7602333 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:939913 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:939913 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:939913 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:7506762 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:7506762 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:7506762 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7506762 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:939913 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:939913 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:939913 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7472477 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:7506762 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:7602333 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:939913 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20160114 MGI PMID:25198651 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0003199 calcified muscle IAGP N RGD:5509061 20141003 MGI PMID:7602333 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0003381 vitreal fibroplasia IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20111116 MGI 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0004220 abnormal peripheral nervous system regeneration IAGP N RGD:5509061 20141003 MGI PMID:7472477 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:7506762 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:7602333 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:939913 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0004510 myositis IAGP N RGD:5509061 20160114 MGI PMID:25198651 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20220512 MGI PMID:34142127 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:7602333 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19797173 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:19017726 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0006200 vitreous body deposition IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0008509 disorganized retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0008520 disorganized retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:7602333 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20160114 MGI PMID:25198651 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:7602333 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20160114 MGI PMID:25198651 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:7602333 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20160114 MGI PMID:25198651 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:7506762 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:7602333 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20160114 MGI PMID:25198651 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0009415 skeletal muscle degeneration IEA N RGD:5509061 20111116 MGI 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0009420 skeletal muscle endomysial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:7506762 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16111892 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:7602333 1318928 Large1 LARGE xylosyl- and glucuronyltransferase 1 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:7602333 1318929 Dbx1 developing brain homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16041369 1318929 Dbx1 developing brain homeobox 1 gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20141003 MGI PMID:20680010 1318929 Dbx1 developing brain homeobox 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151217 MGI PMID:25864637 1318929 Dbx1 developing brain homeobox 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:20680010 1318929 Dbx1 developing brain homeobox 1 gene MP:0001752 abnormal hypothalamus secretion IAGP N RGD:5509061 20151217 MGI PMID:25864637 1318929 Dbx1 developing brain homeobox 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:20680010 1318929 Dbx1 developing brain homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151217 MGI PMID:25864637 1318929 Dbx1 developing brain homeobox 1 gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11239429 1318929 Dbx1 developing brain homeobox 1 gene MP:0003462 abnormal response to novel odor IAGP N RGD:5509061 20151217 MGI PMID:25864637 1318929 Dbx1 developing brain homeobox 1 gene MP:0005267 abnormal olfactory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16041369 1318929 Dbx1 developing brain homeobox 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20151217 MGI PMID:25864637 1318929 Dbx1 developing brain homeobox 1 gene MP:0005423 abnormal somatic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15134635 1318929 Dbx1 developing brain homeobox 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20151217 MGI PMID:25864637 1318929 Dbx1 developing brain homeobox 1 gene MP:0010745 abnormal pre-Botzinger complex morphology IAGP N RGD:5509061 20141003 MGI PMID:20680010 1318929 Dbx1 developing brain homeobox 1 gene MP:0010746 abnormal pre-Botzinger complex physiology IAGP N RGD:5509061 20141003 MGI PMID:20680010 1318929 Dbx1 developing brain homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11239429 1318929 Dbx1 developing brain homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20680010 1318929 Dbx1 developing brain homeobox 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20151217 MGI PMID:25864637 1318929 Dbx1 developing brain homeobox 1 gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20151217 MGI PMID:25864637 1318929 Dbx1 developing brain homeobox 1 gene MP:0021102 abnormal ventral interneuron 0 morphology IAGP N RGD:5509061 20220310 MGI PMID:11239429 1318929 Dbx1 developing brain homeobox 1 gene MP:0021102 abnormal ventral interneuron 0 morphology IAGP N RGD:5509061 20220310 MGI PMID:15134635 1318929 Dbx1 developing brain homeobox 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:25864637 1318932 Slc26a8 solute carrier family 26, member 8 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17517695 1318932 Slc26a8 solute carrier family 26, member 8 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17517695 1318932 Slc26a8 solute carrier family 26, member 8 gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20190912 MGI PMID:17517695 1318932 Slc26a8 solute carrier family 26, member 8 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:17517695 1318932 Slc26a8 solute carrier family 26, member 8 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:17517695 1318932 Slc26a8 solute carrier family 26, member 8 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:17517695 1318932 Slc26a8 solute carrier family 26, member 8 gene MP:0009242 thin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:17517695 1318932 Slc26a8 solute carrier family 26, member 8 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:17517695 1318932 Slc26a8 solute carrier family 26, member 8 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:17517695 1318932 Slc26a8 solute carrier family 26, member 8 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:17517695 1318932 Slc26a8 solute carrier family 26, member 8 gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17517695 1318932 Slc26a8 solute carrier family 26, member 8 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:17517695 1318935 Alg5 ALG5 dolichyl-phosphate beta-glucosyltransferase gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15755804 1318935 Alg5 ALG5 dolichyl-phosphate beta-glucosyltransferase gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15755804 1318935 Alg5 ALG5 dolichyl-phosphate beta-glucosyltransferase gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15755804 1318935 Alg5 ALG5 dolichyl-phosphate beta-glucosyltransferase gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0000746 weakness IAGP N RGD:5509061 20150430 MGI PMID:24764192 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20151224 MGI PMID:25779931 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20150430 MGI PMID:24764192 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0001147 small testis IAGP N RGD:5509061 20151224 MGI PMID:25779931 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151224 MGI PMID:25779931 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20150430 MGI PMID:24764192 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0001297 microphthalmia IAGP N RGD:5509061 20151224 MGI PMID:25779931 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0001317 abnormal pupil morphology IAGP N RGD:5509061 20150430 MGI PMID:24764192 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0001393 ataxia IAGP N RGD:5509061 20151224 MGI PMID:25779931 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0001405 impaired coordination IAGP N RGD:5509061 20151224 MGI PMID:25779931 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0001406 abnormal gait IAGP N RGD:5509061 20151224 MGI PMID:25779931 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0001513 limb grasping IAGP N RGD:5509061 20150430 MGI PMID:24764192 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0001513 limb grasping IAGP N RGD:5509061 20151224 MGI PMID:25779931 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20151224 MGI PMID:25779931 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0002003 miotic pupil IAGP N RGD:5509061 20230713 MGI PMID:24764192 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0002638 abnormal pupillary reflex IAGP N RGD:5509061 20150430 MGI PMID:24764192 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20150430 MGI PMID:24764192 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20150430 MGI PMID:24764192 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0003994 abnormal dorsal spinal root morphology IAGP N RGD:5509061 20151224 MGI PMID:25779931 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0005405 axon degeneration IAGP N RGD:5509061 20151224 MGI PMID:25779931 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20151224 MGI PMID:25779931 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20151224 MGI PMID:25779931 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0009121 increased white fat cell lipid droplet size IAGP N RGD:5509061 20150430 MGI PMID:24764192 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20150430 MGI PMID:24764192 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20150430 MGI PMID:24764192 1318942 Rab18 RAB18, member RAS oncogene family gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20161013 MGI PMID:24764192 1318944 Htra2 HtrA serine peptidase 2 gene MP:0000416 sparse hair IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20200310 MGI PMID:18288109 1318944 Htra2 HtrA serine peptidase 2 gene MP:0000692 small spleen IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20200310 MGI PMID:8325640 1318944 Htra2 HtrA serine peptidase 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20200310 MGI PMID:12009762 1318944 Htra2 HtrA serine peptidase 2 gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20200310 MGI PMID:8325640 1318944 Htra2 HtrA serine peptidase 2 gene MP:0000753 paralysis IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:12009762 1318944 Htra2 HtrA serine peptidase 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20200310 MGI PMID:8325640 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:8325640 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:8325640 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:9806835 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20200310 MGI PMID:12009762 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:8325640 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:9806835 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20200310 MGI PMID:12009762 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20200310 MGI PMID:8325640 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20200310 MGI PMID:9806835 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:12009762 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:8325640 1318944 Htra2 HtrA serine peptidase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:9806835 1318944 Htra2 HtrA serine peptidase 2 gene MP:0002064 seizures IAGP N RGD:5509061 20200310 MGI PMID:9806835 1318944 Htra2 HtrA serine peptidase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:8325640 1318944 Htra2 HtrA serine peptidase 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:12009762 1318944 Htra2 HtrA serine peptidase 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:12009762 1318944 Htra2 HtrA serine peptidase 2 gene MP:0002183 gliosis IAGP N RGD:5509061 20200310 MGI PMID:12009762 1318944 Htra2 HtrA serine peptidase 2 gene MP:0002188 small heart IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200310 MGI PMID:12009762 1318944 Htra2 HtrA serine peptidase 2 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20200310 MGI PMID:9806835 1318944 Htra2 HtrA serine peptidase 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20200310 MGI PMID:18288109 1318944 Htra2 HtrA serine peptidase 2 gene MP:0002690 akinesia IAGP N RGD:5509061 20200310 MGI PMID:12009762 1318944 Htra2 HtrA serine peptidase 2 gene MP:0002690 akinesia IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0003242 loss of basal ganglia neurons IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20200310 MGI PMID:18288109 1318944 Htra2 HtrA serine peptidase 2 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20200310 MGI PMID:8325640 1318944 Htra2 HtrA serine peptidase 2 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20200310 MGI PMID:18288109 1318944 Htra2 HtrA serine peptidase 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:18288109 1318944 Htra2 HtrA serine peptidase 2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20200310 MGI PMID:12009762 1318944 Htra2 HtrA serine peptidase 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0005323 dystonia IAGP N RGD:5509061 20200310 MGI PMID:12009762 1318944 Htra2 HtrA serine peptidase 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200310 MGI PMID:8325640 1318944 Htra2 HtrA serine peptidase 2 gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:18288109 1318944 Htra2 HtrA serine peptidase 2 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20200310 MGI PMID:18288109 1318944 Htra2 HtrA serine peptidase 2 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20200310 MGI PMID:18288109 1318944 Htra2 HtrA serine peptidase 2 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20200310 MGI PMID:15509788 1318944 Htra2 HtrA serine peptidase 2 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20200310 MGI PMID:12009762 1318944 Htra2 HtrA serine peptidase 2 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20200310 MGI PMID:12009762 1318944 Htra2 HtrA serine peptidase 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:9806835 1318944 Htra2 HtrA serine peptidase 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1318944 Htra2 HtrA serine peptidase 2 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0011634 abnormal mitochondrial inner membrane morphology IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318944 Htra2 HtrA serine peptidase 2 gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20200310 MGI PMID:25531304 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0002965 increased circulating serum albumin level IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0004892 increased adiponectin level IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0005337 abnormal retroperitoneal fat pad morphology IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20161229 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240718 MGI PMID:22961760 1318949 Hint2 histidine triad nucleotide binding protein 2 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:22961760 1318951 Meox1 mesenchyme homeobox 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0000138 absent vertebrae IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0000151 absent ribs IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0000592 short tail IEA N RGD:5509061 20230928 MGI 1318951 Meox1 mesenchyme homeobox 1 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20230928 MGI 1318951 Meox1 mesenchyme homeobox 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22659386 1318951 Meox1 mesenchyme homeobox 1 gene MP:0002632 vestigial tail IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0003051 curly tail IEA N RGD:5509061 20230928 MGI 1318951 Meox1 mesenchyme homeobox 1 gene MP:0003358 abnormal hypaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0004248 abnormal epaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0004653 absent caudal vertebrae IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0008832 hemivertebra IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12925591 1318951 Meox1 mesenchyme homeobox 1 gene MP:0030286 occipital bone hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:12925591 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20622884 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20622884 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:20622884 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:20622884 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15342461 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20622884 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:20622884 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20622884 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:20622884 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0031152 subcutaneous hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:19633199 1318954 Zfp36l2 zinc finger protein 36, C3H type-like 2 gene MP:0031154 intestinal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:19633199 1318956 Sema5b sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318956 Sema5b sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318956 Sema5b sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318956 Sema5b sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B gene MP:0005018 decreased T cell number IEA N RGD:5509061 20141003 MGI 1318956 Sema5b sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318956 Sema5b sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318956 Sema5b sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318956 Sema5b sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318956 Sema5b sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318956 Sema5b sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318956 Sema5b sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318956 Sema5b sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:21835343 1318959 Csrnp2 cysteine-serine-rich nuclear protein 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17726538 1318959 Csrnp2 cysteine-serine-rich nuclear protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17726538 1318966 Col19a1 collagen, type XIX, alpha 1 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:15302855 1318966 Col19a1 collagen, type XIX, alpha 1 gene MP:0000467 abnormal esophagus morphology IAGP N RGD:5509061 20141003 MGI PMID:15302855 1318966 Col19a1 collagen, type XIX, alpha 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15302855 1318966 Col19a1 collagen, type XIX, alpha 1 gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:15302855 1318966 Col19a1 collagen, type XIX, alpha 1 gene MP:0003158 dysphagia IAGP N RGD:5509061 20141003 MGI PMID:15302855 1318966 Col19a1 collagen, type XIX, alpha 1 gene MP:0003159 abnormal esophageal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15302855 1318966 Col19a1 collagen, type XIX, alpha 1 gene MP:0003160 abnormal esophagus development IAGP N RGD:5509061 20141003 MGI PMID:15302855 1318966 Col19a1 collagen, type XIX, alpha 1 gene MP:0004548 dilated esophagus IAGP N RGD:5509061 20141003 MGI PMID:15302855 1318966 Col19a1 collagen, type XIX, alpha 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:15302855 1318966 Col19a1 collagen, type XIX, alpha 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15302855 1318971 Faap20 Fanconi anemia core complex associated protein 20 gene MP:0001127 small ovary IAGP N RGD:5509061 20151112 MGI PMID:25917546 1318971 Faap20 Fanconi anemia core complex associated protein 20 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20151112 MGI PMID:25917546 1318971 Faap20 Fanconi anemia core complex associated protein 20 gene MP:0001147 small testis IAGP N RGD:5509061 20151112 MGI PMID:25917546 1318971 Faap20 Fanconi anemia core complex associated protein 20 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20151112 MGI PMID:25917546 1318971 Faap20 Fanconi anemia core complex associated protein 20 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20151112 MGI PMID:25917546 1318971 Faap20 Fanconi anemia core complex associated protein 20 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20151112 MGI PMID:25917546 1318971 Faap20 Fanconi anemia core complex associated protein 20 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20151112 MGI PMID:25917546 1318971 Faap20 Fanconi anemia core complex associated protein 20 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20151112 MGI PMID:25917546 1318971 Faap20 Fanconi anemia core complex associated protein 20 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20151112 MGI PMID:25917546 1318971 Faap20 Fanconi anemia core complex associated protein 20 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20151112 MGI PMID:25917546 1318973 Tax1bp3 Tax1 (human T cell leukemia virus type I) binding protein 3 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1318973 Tax1bp3 Tax1 (human T cell leukemia virus type I) binding protein 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1318973 Tax1bp3 Tax1 (human T cell leukemia virus type I) binding protein 3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1318973 Tax1bp3 Tax1 (human T cell leukemia virus type I) binding protein 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318975 Brd3 bromodomain containing 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20221215 MGI 1318975 Brd3 bromodomain containing 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20220811 MGI 1318975 Brd3 bromodomain containing 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220811 MGI 1318975 Brd3 bromodomain containing 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1318975 Brd3 bromodomain containing 3 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220811 MGI 1318975 Brd3 bromodomain containing 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1318975 Brd3 bromodomain containing 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220811 MGI 1318977 Fkbp6 FK506 binding protein 6 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12764197 1318977 Fkbp6 FK506 binding protein 6 gene MP:0001513 limb grasping IEA N RGD:5509061 20201022 MGI 1318977 Fkbp6 FK506 binding protein 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12764197 1318977 Fkbp6 FK506 binding protein 6 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:12764197 1318977 Fkbp6 FK506 binding protein 6 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1318977 Fkbp6 FK506 binding protein 6 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12764197 1318977 Fkbp6 FK506 binding protein 6 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12764197 1318979 Nprl2 NPR2 like, GATOR1 complex subunit gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20160929 MGI PMID:26166573 1318979 Nprl2 NPR2 like, GATOR1 complex subunit gene MP:0000603 pale liver IAGP N RGD:5509061 20160929 MGI PMID:26166573 1318979 Nprl2 NPR2 like, GATOR1 complex subunit gene MP:0001293 anophthalmia IAGP N RGD:5509061 20160929 MGI PMID:26166573 1318979 Nprl2 NPR2 like, GATOR1 complex subunit gene MP:0001297 microphthalmia IAGP N RGD:5509061 20160929 MGI PMID:26166573 1318979 Nprl2 NPR2 like, GATOR1 complex subunit gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20160929 MGI PMID:26166573 1318979 Nprl2 NPR2 like, GATOR1 complex subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160929 MGI PMID:26166573 1318979 Nprl2 NPR2 like, GATOR1 complex subunit gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20160929 MGI PMID:26166573 1318979 Nprl2 NPR2 like, GATOR1 complex subunit gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20160929 MGI PMID:26166573 1318979 Nprl2 NPR2 like, GATOR1 complex subunit gene MP:0014399 decreased hematopoietic precursor cell number IAGP N RGD:5509061 20240321 MGI PMID:26166573 1318982 Fam168a family with sequence similarity 168, member A gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1318982 Fam168a family with sequence similarity 168, member A gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1318982 Fam168a family with sequence similarity 168, member A gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201022 MGI 1318982 Fam168a family with sequence similarity 168, member A gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1318987 Ythdf1 YTH N6-methyladenosine RNA binding protein 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20210722 MGI PMID:30401835 1318987 Ythdf1 YTH N6-methyladenosine RNA binding protein 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20210722 MGI PMID:30401835 1318987 Ythdf1 YTH N6-methyladenosine RNA binding protein 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20210722 MGI PMID:30401835 1318987 Ythdf1 YTH N6-methyladenosine RNA binding protein 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20210722 MGI PMID:30843071 1318987 Ythdf1 YTH N6-methyladenosine RNA binding protein 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20210722 MGI PMID:30401835 1318987 Ythdf1 YTH N6-methyladenosine RNA binding protein 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20210722 MGI PMID:30401835 1318987 Ythdf1 YTH N6-methyladenosine RNA binding protein 1 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20210722 MGI PMID:30843071 1318987 Ythdf1 YTH N6-methyladenosine RNA binding protein 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20210722 MGI PMID:30401835 1318987 Ythdf1 YTH N6-methyladenosine RNA binding protein 1 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20210722 MGI PMID:30401835 1318987 Ythdf1 YTH N6-methyladenosine RNA binding protein 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20210128 MGI PMID:32943573 1318987 Ythdf1 YTH N6-methyladenosine RNA binding protein 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20210128 MGI PMID:32943573 1318987 Ythdf1 YTH N6-methyladenosine RNA binding protein 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20210722 MGI PMID:30401835 1318987 Ythdf1 YTH N6-methyladenosine RNA binding protein 1 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20210722 MGI PMID:30401835 1318987 Ythdf1 YTH N6-methyladenosine RNA binding protein 1 gene MP:0014252 abnormal paired-pulse ratio IAGP N RGD:5509061 20230706 MGI PMID:30401835 1318987 Ythdf1 YTH N6-methyladenosine RNA binding protein 1 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20210722 MGI PMID:30401835 1318990 Anxa10 annexin A10 gene MP:0003718 maternal effect IAGP N RGD:5509061 20170518 MGI PMID:27881083 1318992 Gpatch1 G patch domain containing 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318992 Gpatch1 G patch domain containing 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318992 Gpatch1 G patch domain containing 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1318992 Gpatch1 G patch domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1318994 Anapc10 anaphase promoting complex subunit 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1318994 Anapc10 anaphase promoting complex subunit 10 gene MP:0012000 abnormal limb position IEA N RGD:5509061 20240523 MGI 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210520 MGI 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:20858856 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0000467 abnormal esophagus morphology IEA N RGD:5509061 20190502 MGI 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20190502 MGI 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20190502 MGI 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0000705 athymia IEA N RGD:5509061 20190502 MGI 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0001293 anophthalmia IEA N RGD:5509061 20190502 MGI 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20858856 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:20858856 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20190502 MGI 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20858856 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0002282 abnormal trachea morphology IEA N RGD:5509061 20190502 MGI 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:20858856 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20858856 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:20858856 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0008024 absent lymph nodes IEA N RGD:5509061 20190502 MGI 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20858856 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20858856 1318996 Mmp15 matrix metallopeptidase 15 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1318998 Tnpo3 transportin 3 gene MP:0008762 embryonic lethality IEA N RGD:5509061 20141003 MGI 1319002 Tmod4 tropomodulin 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26586224 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:16043865 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16043865 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16043865 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16043865 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0004524 short cochlear hair cell stereocilia IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:20660251 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:20660251 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18662770 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:18662770 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:20660251 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16043865 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:16043865 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:16043865 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:16043865 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18662770 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20660251 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0014409 decreased distortion product otoacoustic emission amplitude IAGP N RGD:5509061 20240405 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0020811 abnormal photoreceptor outer segment size IAGP N RGD:5509061 20200206 MGI PMID:30082328 1319004 Fscn2 fascin actin-bundling protein 2 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:16043865 1319006 Gjd3 gap junction protein, delta 3 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:16571663 1319006 Gjd3 gap junction protein, delta 3 gene MP:0006141 abnormal atrioventricular node conduction IAGP N RGD:5509061 20141003 MGI PMID:16571663 1319006 Gjd3 gap junction protein, delta 3 gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:22982984 1319006 Gjd3 gap junction protein, delta 3 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:22982984 1319006 Gjd3 gap junction protein, delta 3 gene MP:0010511 shortened PR interval IAGP N RGD:5509061 20141003 MGI PMID:22982984 1319006 Gjd3 gap junction protein, delta 3 gene MP:0011953 prolonged PQ interval IAGP N RGD:5509061 20141003 MGI PMID:22982984 1319006 Gjd3 gap junction protein, delta 3 gene MP:0011954 shortened PQ interval IAGP N RGD:5509061 20141003 MGI PMID:16571663 1319010 Bnip2 BCL2/adenovirus E1B interacting protein 2 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20201231 MGI 1319010 Bnip2 BCL2/adenovirus E1B interacting protein 2 gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20160421 MGI 1319010 Bnip2 BCL2/adenovirus E1B interacting protein 2 gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20160421 MGI 1319010 Bnip2 BCL2/adenovirus E1B interacting protein 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1319010 Bnip2 BCL2/adenovirus E1B interacting protein 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1319010 Bnip2 BCL2/adenovirus E1B interacting protein 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1319010 Bnip2 BCL2/adenovirus E1B interacting protein 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20181227 MGI 1319010 Bnip2 BCL2/adenovirus E1B interacting protein 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1319010 Bnip2 BCL2/adenovirus E1B interacting protein 2 gene MP:0010096 abnormal incisor color IEA N RGD:5509061 20181227 MGI 1319014 H13 histocompatibility 13 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0000151 absent ribs IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201231 MGI 1319014 H13 histocompatibility 13 gene MP:0000520 absent kidney IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0000819 abnormal olfactory bulb morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0000914 exencephaly IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0000963 fused dorsal root ganglion IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0001014 absent superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319014 H13 histocompatibility 13 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0002177 abnormal outer ear morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0002766 situs inversus IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319014 H13 histocompatibility 13 gene MP:0002858 abnormal posterior semicircular canal morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0002951 small thyroid gland IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0002989 small kidney IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0003178 left pulmonary isomerism IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0003632 abnormal nervous system morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0004110 transposition of great arteries IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0004160 retroesophageal right subclavian artery IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0004259 small placenta IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319014 H13 histocompatibility 13 gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0004607 abnormal cervical atlas morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0004665 abnormal stapedial artery morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0004666 absent stapedial artery IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0004686 decreased length of long bones IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319014 H13 histocompatibility 13 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319014 H13 histocompatibility 13 gene MP:0006425 absent Mullerian ducts IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0008023 abnormal styloid process morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0008128 abnormal brain internal capsule morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319014 H13 histocompatibility 13 gene MP:0008923 thoracoschisis IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0009770 abnormal optic chiasm morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0009820 abnormal liver vasculature morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1319014 H13 histocompatibility 13 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0010439 abnormal hepatic vein morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0010490 abnormal inferior vena cava valve morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0010602 abnormal pulmonary valve cusp morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319014 H13 histocompatibility 13 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1319014 H13 histocompatibility 13 gene MP:0013824 abnormal hypoglossal canal morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013826 absent hypoglossal canal IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013855 absent celiac artery IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013858 abnormal azygos vein topology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013861 abnormal pancreas topology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013864 enlarged paraumbilical vein IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013871 abnormal stapedial artery topology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013915 abnormal brachial plexus formation IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013936 abnormal thymus topology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013966 abnormal infrahyoid muscle morphology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013968 multiple persisting craniopharyngeal ducts IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013977 symmetric azygos veins IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013985 abnormal umbilical vein topology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013992 persistent dorsal ophthalmic artery IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0013996 abnormal vertebral artery origin IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0014006 absent posterior communicating artery IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0014018 embryo tumor IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0014023 abnormal intestine placement IEA N RGD:5509061 20170504 MGI 1319014 H13 histocompatibility 13 gene MP:0020493 absent inferior vena cava IEA N RGD:5509061 20180628 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0000111 cleft palate IEA N RGD:5509061 20210520 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20201022 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20201022 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0000564 syndactyly IEA N RGD:5509061 20210520 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0000601 small liver IEA N RGD:5509061 20210128 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20200514 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20201022 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20201022 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210826 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20201022 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20201022 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20201022 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20240523 MGI 1319016 Rgl1 ral guanine nucleotide dissociation stimulator,-like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319018 Rrh retinal pigment epithelium derived rhodopsin homolog gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20191114 MGI PMID:29109151 1319020 Ptdss1 phosphatidylserine synthase 1 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20170105 MGI 1319020 Ptdss1 phosphatidylserine synthase 1 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:18343815 1319020 Ptdss1 phosphatidylserine synthase 1 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20160421 MGI 1319020 Ptdss1 phosphatidylserine synthase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18343815 1319020 Ptdss1 phosphatidylserine synthase 1 gene MP:0012361 decreased large unstained cell number IEA N RGD:5509061 20211021 MGI 1319022 Ap3b2 adaptor-related protein complex 3, beta 2 subunit gene MP:0000745 tremors IEA N RGD:5509061 20200514 MGI 1319022 Ap3b2 adaptor-related protein complex 3, beta 2 subunit gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20200514 MGI 1319022 Ap3b2 adaptor-related protein complex 3, beta 2 subunit gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15537701 1319022 Ap3b2 adaptor-related protein complex 3, beta 2 subunit gene MP:0001406 abnormal gait IEA N RGD:5509061 20200514 MGI 1319022 Ap3b2 adaptor-related protein complex 3, beta 2 subunit gene MP:0003492 abnormal involuntary movement IEA N RGD:5509061 20141003 MGI 1319022 Ap3b2 adaptor-related protein complex 3, beta 2 subunit gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15537701 1319022 Ap3b2 adaptor-related protein complex 3, beta 2 subunit gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:15537701 1319022 Ap3b2 adaptor-related protein complex 3, beta 2 subunit gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20160428 MGI PMID:25917818 1319022 Ap3b2 adaptor-related protein complex 3, beta 2 subunit gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20141003 MGI 1319027 Mcoln1 mucolipin 1 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:21111738 1319027 Mcoln1 mucolipin 1 gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:21111738 1319027 Mcoln1 mucolipin 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21111738 1319027 Mcoln1 mucolipin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:23063126 1319027 Mcoln1 mucolipin 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:21111738 1319027 Mcoln1 mucolipin 1 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21111738 1319027 Mcoln1 mucolipin 1 gene MP:0004731 increased circulating gastrin level IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0004731 increased circulating gastrin level IAGP N RGD:5509061 20141003 MGI PMID:21111738 1319027 Mcoln1 mucolipin 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20141003 MGI PMID:21111738 1319027 Mcoln1 mucolipin 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319027 Mcoln1 mucolipin 1 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:17924347 1319029 Cobll1 Cobl-like 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1319029 Cobll1 Cobl-like 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1319029 Cobll1 Cobl-like 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1319029 Cobll1 Cobl-like 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1319029 Cobll1 Cobl-like 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1319029 Cobll1 Cobl-like 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 1319029 Cobll1 Cobl-like 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20230601 MGI 1319029 Cobll1 Cobl-like 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1319029 Cobll1 Cobl-like 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1319029 Cobll1 Cobl-like 1 gene MP:0003918 decreased kidney weight IEA N RGD:5509061 20240523 MGI 1319029 Cobll1 Cobl-like 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20240523 MGI 1319029 Cobll1 Cobl-like 1 gene MP:0013129 abnormal tooth color IEA N RGD:5509061 20230601 MGI 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15226267 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20160811 MGI 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:15226267 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:16221973 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20160811 MGI 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:15226267 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:9582278 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11526516 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12901790 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15226267 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:11526516 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:12901790 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15226267 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220519 MGI 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20221215 MGI 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20221215 MGI 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0008402 increased cellular sensitivity to alkylating agents IAGP N RGD:5509061 20141003 MGI PMID:9582278 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15226267 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:15226267 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15226267 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15226267 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9582278 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319032 Mtf1 metal response element binding transcription factor 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1319033 Vstm2a V-set and transmembrane domain containing 2A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1319033 Vstm2a V-set and transmembrane domain containing 2A gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 1319033 Vstm2a V-set and transmembrane domain containing 2A gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20220811 MGI 1319033 Vstm2a V-set and transmembrane domain containing 2A gene MP:0002989 small kidney IEA N RGD:5509061 20220519 MGI 1319033 Vstm2a V-set and transmembrane domain containing 2A gene MP:0003068 enlarged kidney IEA N RGD:5509061 20220519 MGI 1319033 Vstm2a V-set and transmembrane domain containing 2A gene MP:0003604 single kidney IEA N RGD:5509061 20220519 MGI 1319033 Vstm2a V-set and transmembrane domain containing 2A gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20220519 MGI 1319038 Wapl WAPL cohesin release factor gene MP:0001697 abnormal embryo size IAGP N RGD:5509061 20230629 MGI PMID:36449618 1319038 Wapl WAPL cohesin release factor gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:23975099 1319038 Wapl WAPL cohesin release factor gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:23975099 1319038 Wapl WAPL cohesin release factor gene MP:0006204 embryonic lethality before implantation IAGP N RGD:5509061 20230629 MGI PMID:36449618 1319038 Wapl WAPL cohesin release factor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23975099 1319038 Wapl WAPL cohesin release factor gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20230629 MGI PMID:36449618 1319038 Wapl WAPL cohesin release factor gene MP:0011705 absent fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:23975099 1319040 Pdcd7 programmed cell death 7 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0000601 small liver IEA N RGD:5509061 20220519 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0001148 enlarged testis IEA N RGD:5509061 20220811 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20220811 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210520 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0001714 absent trophoblast giant cells IEA N RGD:5509061 20240926 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20240926 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0002626 increased heart rate IEA N RGD:5509061 20231207 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0004964 absent inner cell mass IEA N RGD:5509061 20240926 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20221215 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20220519 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0010507 shortened RR interval IEA N RGD:5509061 20231207 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220811 MGI 1319040 Pdcd7 programmed cell death 7 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240926 MGI 1319044 Lmcd1 LIM and cysteine-rich domains 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1319044 Lmcd1 LIM and cysteine-rich domains 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1319044 Lmcd1 LIM and cysteine-rich domains 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1319044 Lmcd1 LIM and cysteine-rich domains 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230601 MGI 1319048 Efs embryonal Fyn-associated substrate gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16314525 1319048 Efs embryonal Fyn-associated substrate gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:16314525 1319048 Efs embryonal Fyn-associated substrate gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:16314525 1319048 Efs embryonal Fyn-associated substrate gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:16314525 1319048 Efs embryonal Fyn-associated substrate gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16314525 1319048 Efs embryonal Fyn-associated substrate gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16314525 1319048 Efs embryonal Fyn-associated substrate gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16314525 1319048 Efs embryonal Fyn-associated substrate gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:16314525 1319048 Efs embryonal Fyn-associated substrate gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:16314525 1319048 Efs embryonal Fyn-associated substrate gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16314525 1319048 Efs embryonal Fyn-associated substrate gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:16314525 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20141003 MGI 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0000149 abnormal scapula morphology IEA N RGD:5509061 20141003 MGI 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0000160 kyphosis IEA N RGD:5509061 20150430 MGI 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0000552 abnormal radius morphology IEA N RGD:5509061 20150430 MGI 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20141003 MGI 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20160114 MGI 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20201231 MGI 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0005108 abnormal ulna morphology IEA N RGD:5509061 20150430 MGI 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20201231 MGI 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20170105 MGI 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1319051 Tram2 translocating chain-associating membrane protein 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1319053 Ddost dolichyl-di-phosphooligosaccharide-protein glycotransferase gene MP:0000692 small spleen IEA N RGD:5509061 20160811 MGI 1319053 Ddost dolichyl-di-phosphooligosaccharide-protein glycotransferase gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20160811 MGI 1319053 Ddost dolichyl-di-phosphooligosaccharide-protein glycotransferase gene MP:0002768 small adrenal glands IEA N RGD:5509061 20160811 MGI 1319053 Ddost dolichyl-di-phosphooligosaccharide-protein glycotransferase gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220519 MGI 1319053 Ddost dolichyl-di-phosphooligosaccharide-protein glycotransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1319053 Ddost dolichyl-di-phosphooligosaccharide-protein glycotransferase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1319053 Ddost dolichyl-di-phosphooligosaccharide-protein glycotransferase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1319055 Icam4 intercellular adhesion molecule 4, Landsteiner-Wiener blood group gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:16690966 1319057 Nagpa N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase gene MP:0003174 increased lysosomal enzyme secretion IAGP N RGD:5509061 20141003 MGI PMID:19710420 1319060 Melk maternal embryonic leucine zipper kinase gene MP:0005518 abnormal pancreas regeneration IAGP N RGD:5509061 20160317 MGI PMID:25194022 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0001128 ovary hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0001934 increased litter size IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20170105 MGI 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20160114 MGI 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0002681 increased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0002808 abnormal barbering behavior IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0003378 early sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0004909 increased seminal vesicle weight IAGP N RGD:5509061 20141204 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0004928 increased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0014272 increased ovary secretion IAGP N RGD:5509061 20230810 MGI PMID:18431515 1319068 Chst8 carbohydrate sulfotransferase 8 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1319071 Nlrp9b NLR family, pyrin domain containing 9B gene MP:0000274 enlarged heart IEA N RGD:5509061 20200402 MGI 1319071 Nlrp9b NLR family, pyrin domain containing 9B gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200402 MGI 1319071 Nlrp9b NLR family, pyrin domain containing 9B gene MP:0001147 small testis IEA N RGD:5509061 20200402 MGI 1319071 Nlrp9b NLR family, pyrin domain containing 9B gene MP:0001935 decreased litter size IAGP N RGD:5509061 20210415 MGI PMID:32413845 1319071 Nlrp9b NLR family, pyrin domain containing 9B gene MP:0002293 long gestation period IAGP N RGD:5509061 20210415 MGI PMID:32413845 1319071 Nlrp9b NLR family, pyrin domain containing 9B gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20210415 MGI PMID:32413845 1319071 Nlrp9b NLR family, pyrin domain containing 9B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20210415 MGI PMID:32413845 1319071 Nlrp9b NLR family, pyrin domain containing 9B gene MP:0005036 diarrhea IAGP N RGD:5509061 20180111 MGI PMID:28636595 1319071 Nlrp9b NLR family, pyrin domain containing 9B gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20180111 MGI PMID:28636595 1319071 Nlrp9b NLR family, pyrin domain containing 9B gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20210415 MGI PMID:32413845 1319071 Nlrp9b NLR family, pyrin domain containing 9B gene MP:0012128 abnormal blastocyst formation IAGP N RGD:5509061 20210415 MGI PMID:32413845 1319071 Nlrp9b NLR family, pyrin domain containing 9B gene MP:0012129 failure of blastocyst formation IAGP N RGD:5509061 20210415 MGI PMID:32413845 1319071 Nlrp9b NLR family, pyrin domain containing 9B gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:28636595 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:9768756 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000321 increased bone marrow cell number IEA N RGD:5509061 20111116 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000346 broad head IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11884426 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000618 small salivary gland IAGP N RGD:5509061 20141003 MGI PMID:7541529 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:22773809 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000687 small lymphoid organs IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000687 small lymphoid organs IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:10805749 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:9768756 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000726 absent lymphocyte IAGP N RGD:5509061 20141003 MGI PMID:9103418 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:17668421 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001260 increased body weight IEA N RGD:5509061 20190411 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:18563383 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:23747725 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:10805749 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:17662890 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001790 abnormal immune system physiology IEA N RGD:5509061 20120119 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9103418 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9768756 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9103418 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9768756 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:9103418 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001860 liver inflammation IEA N RGD:5509061 20111116 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001862 interstitial pneumonia IEA N RGD:5509061 20111116 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:7957574 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:10878379 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:17668421 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:10805749 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:11280730 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7589844 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9103418 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:7541529 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8339285 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9584189 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18563383 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9103418 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9584189 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:15699352 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8094405 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002223 lymphoid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002367 abnormal thymus lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22773809 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:8320959 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8094405 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15470055 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10725754 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8094405 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002459 abnormal B cell physiology IEA N RGD:5509061 20141003 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002473 impaired complement classical pathway IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002494 increased IgM level IEA N RGD:5509061 20180222 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002619 abnormal lymphocyte morphology IEA N RGD:5509061 20141003 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:15699352 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23747725 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:7541529 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002816 colitis IEA N RGD:5509061 20111116 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17668421 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002879 increased cellular sensitivity to X-ray irradiation IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:15699352 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:23747725 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:7541529 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:7541529 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20230824 MGI PMID:12897131 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:17668421 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:7541529 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:9768756 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:12750251 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004503 decreased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:17668421 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10725754 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:11120869 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:12525697 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:12525697 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20160218 MGI PMID:12361980 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:19450527 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22761313 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0004978 decreased B-1 B cell number IEA N RGD:5509061 20180927 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8094405 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005014 increased B cell number IEA N RGD:5509061 20180222 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005015 increased T cell number IEA N RGD:5509061 20190530 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17668421 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005036 diarrhea IEA N RGD:5509061 20111116 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9768756 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:23747725 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15699352 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:7541529 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:9103418 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15308121 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20201022 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:10809058 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:11777954 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:15308121 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:15591949 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:18785974 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:9103418 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0005673 decreased susceptibility to graft versus host disease IAGP N RGD:5509061 20141003 MGI PMID:15591949 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0006198 enophthalmos IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20180927 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:17662890 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008076 abnormal CD4-positive T cell differentiation IEA N RGD:5509061 20190411 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20190411 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008081 abnormal single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8094405 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008097 increased plasma cell number IEA N RGD:5509061 20111116 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008102 lymph node hyperplasia IEA N RGD:5509061 20111116 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008168 decreased B-1a cell number IEA N RGD:5509061 20180222 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20180215 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008195 abnormal professional antigen presenting cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17662890 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008402 increased cellular sensitivity to alkylating agents IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008466 enlarged mesenteric lymph nodes IEA N RGD:5509061 20111116 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008524 increased plasmacytoid dendritic cell number IEA N RGD:5509061 20180215 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:9768756 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008755 abnormal immunoglobulin V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008756 abnormal T cell receptor alpha chain V-J recombination IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008758 abnormal T cell receptor beta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008758 abnormal T cell receptor beta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:9768756 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008758 abnormal T cell receptor beta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008759 abnormal T cell receptor delta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008759 abnormal T cell receptor delta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008761 abnormal immunoglobulin light chain V-J recombination IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:9103418 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008838 decreased transforming growth factor beta level IAGP N RGD:5509061 20141003 MGI PMID:17668421 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15699352 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0009332 abnormal splenocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15308121 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20210722 MGI PMID:31795137 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:17668421 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:17668421 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:17668421 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17668421 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0009481 cecum inflammation IEA N RGD:5509061 20111116 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10677503 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:9768755 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0009856 failure of ejaculation IAGP N RGD:5509061 20141003 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0010250 absent thymus cortex IAGP N RGD:5509061 20160324 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0010373 myeloid hyperplasia IEA N RGD:5509061 20111116 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9103418 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9834083 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180927 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0010845 decreased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180222 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20180927 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190530 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21482716 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0011473 increased urine glycosaminoglycan level IAGP N RGD:5509061 20141003 MGI PMID:17920451 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:17668421 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20190530 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0013741 absent thymus corticomedullary boundary IAGP N RGD:5509061 20150430 MGI PMID:9990036 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0014127 increased thymoma incidence IAGP N RGD:5509061 20160317 MGI PMID:9584189 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0014130 thymus cyst IAGP N RGD:5509061 20160324 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0014130 thymus cyst IAGP N RGD:5509061 20160324 MGI PMID:6823332 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0014130 thymus cyst IAGP N RGD:5509061 20160324 MGI PMID:7995938 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0014130 thymus cyst IAGP N RGD:5509061 20160324 MGI PMID:8806787 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:15879151 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0014269 decreased testes secretion IAGP N RGD:5509061 20230810 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20151015 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0020155 enhanced humoral immune response IEA N RGD:5509061 20180222 MGI 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20230824 MGI PMID:12897131 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0030983 failure of copulatory plug deposition IAGP N RGD:5509061 20191017 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0031628 abnormal intromission IAGP N RGD:5509061 20240718 MGI PMID:17478551 1319073 Prkdc protein kinase, DNA activated, catalytic polypeptide gene MP:0031650 decreased mounting behavior IAGP N RGD:5509061 20240905 MGI PMID:17478551 1319082 Gsdmc gasdermin C gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20230601 MGI 1319082 Gsdmc gasdermin C gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20230601 MGI 1319082 Gsdmc gasdermin C gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1319084 Edc4 enhancer of mRNA decapping 4 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1319084 Edc4 enhancer of mRNA decapping 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1319084 Edc4 enhancer of mRNA decapping 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319085 Scyl3 SCY1-like 3 (S. cerevisiae) gene MP:0000753 paralysis IAGP N RGD:5509061 20200310 MGI PMID:29437892 1319085 Scyl3 SCY1-like 3 (S. cerevisiae) gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20200310 MGI PMID:29437892 1319085 Scyl3 SCY1-like 3 (S. cerevisiae) gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:29437892 1319085 Scyl3 SCY1-like 3 (S. cerevisiae) gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200310 MGI PMID:29437892 1319085 Scyl3 SCY1-like 3 (S. cerevisiae) gene MP:0001255 decreased body height IAGP N RGD:5509061 20200310 MGI PMID:29437892 1319085 Scyl3 SCY1-like 3 (S. cerevisiae) gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:29437892 1319085 Scyl3 SCY1-like 3 (S. cerevisiae) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:29437892 1319085 Scyl3 SCY1-like 3 (S. cerevisiae) gene MP:0002183 gliosis IAGP N RGD:5509061 20200310 MGI PMID:29437892 1319085 Scyl3 SCY1-like 3 (S. cerevisiae) gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:29437892 1319085 Scyl3 SCY1-like 3 (S. cerevisiae) gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:29437892 1319085 Scyl3 SCY1-like 3 (S. cerevisiae) gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20200310 MGI PMID:29437892 1319085 Scyl3 SCY1-like 3 (S. cerevisiae) gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:29437892 1319088 Ngp neutrophilic granule protein gene MP:0001314 cornea opacity IEA N RGD:5509061 20201231 MGI 1319088 Ngp neutrophilic granule protein gene MP:0004952 increased spleen weight IEA N RGD:5509061 20201022 MGI 1319091 S100a5 S100 calcium binding protein A5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141218 MGI PMID:25411495 1319091 S100a5 S100 calcium binding protein A5 gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20141218 MGI PMID:25411495 1319093 Nts neurotensin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:21907138 1319093 Nts neurotensin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21907138 1319093 Nts neurotensin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21907138 1319093 Nts neurotensin gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21907138 1319093 Nts neurotensin gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:21907138 1319093 Nts neurotensin gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:21907138 1319093 Nts neurotensin gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21907138 1319093 Nts neurotensin gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21907138 1319093 Nts neurotensin gene MP:0005457 abnormal percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:21907138 1319093 Nts neurotensin gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21907138 1319093 Nts neurotensin gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11427716 1319093 Nts neurotensin gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21907138 1319093 Nts neurotensin gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21907138 1319093 Nts neurotensin gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21907138 1319093 Nts neurotensin gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20141003 MGI PMID:21907138 1319093 Nts neurotensin gene MP:0014441 decreased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:21907138 1319095 Abca6 ATP-binding cassette, sub-family A member 6 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20210128 MGI 1319095 Abca6 ATP-binding cassette, sub-family A member 6 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20201022 MGI 1319095 Abca6 ATP-binding cassette, sub-family A member 6 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160421 MGI 1319095 Abca6 ATP-binding cassette, sub-family A member 6 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20240523 MGI 1319095 Abca6 ATP-binding cassette, sub-family A member 6 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20221215 MGI 1319097 Cldn9 claudin 9 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:19696885 1319097 Cldn9 claudin 9 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20230119 MGI 1319097 Cldn9 claudin 9 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:19696885 1319097 Cldn9 claudin 9 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20230119 MGI 1319097 Cldn9 claudin 9 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:19696885 1319097 Cldn9 claudin 9 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19696885 1319097 Cldn9 claudin 9 gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:19696885 1319097 Cldn9 claudin 9 gene MP:0004888 abnormal perilymph physiology IAGP N RGD:5509061 20141003 MGI PMID:19696885 1319097 Cldn9 claudin 9 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:19696885 1319097 Cldn9 claudin 9 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:19696885 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:16652367 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:16652367 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:18543318 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:18543318 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:18543318 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:18543318 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18543318 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:18543318 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18543318 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:18543318 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0002898 absent cartilage IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:18543318 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:18543318 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16652367 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16652367 1319099 Sox6 SRY (sex determining region Y)-box 6 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11702786 1319101 Cldn23 claudin 23 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1319101 Cldn23 claudin 23 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20240523 MGI 1319101 Cldn23 claudin 23 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1319104 Usp25 ubiquitin specific peptidase 25 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23042150 1319104 Usp25 ubiquitin specific peptidase 25 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23042150 1319104 Usp25 ubiquitin specific peptidase 25 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:23042150 1319104 Usp25 ubiquitin specific peptidase 25 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23042150 1319104 Usp25 ubiquitin specific peptidase 25 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:23042150 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20181227 MGI 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20181227 MGI 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0000706 small thymus IEA N RGD:5509061 20181227 MGI 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20181227 MGI 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20181227 MGI 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0002883 chromatolysis IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20160915 MGI PMID:24480485 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20160915 MGI PMID:24480485 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20181227 MGI 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20160915 MGI PMID:24480485 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20160915 MGI PMID:24480485 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20151112 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20160915 MGI PMID:24480485 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20160915 MGI PMID:24480485 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0014320 abnormal autopod rotation IAGP N RGD:5509061 20240404 MGI PMID:25860513 1319107 Gdap1 ganglioside-induced differentiation-associated-protein 1 gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20190711 MGI PMID:24480485 1319112 Ppfia1 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1319112 Ppfia1 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1319112 Ppfia1 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1319112 Ppfia1 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319117 Rnaseh1 ribonuclease H1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12667461 1319117 Rnaseh1 ribonuclease H1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12667461 1319117 Rnaseh1 ribonuclease H1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:12667461 1319117 Rnaseh1 ribonuclease H1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:12667461 1319117 Rnaseh1 ribonuclease H1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12667461 1319117 Rnaseh1 ribonuclease H1 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:12667461 1319117 Rnaseh1 ribonuclease H1 gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20141003 MGI PMID:12667461 1319117 Rnaseh1 ribonuclease H1 gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20141003 MGI PMID:12667461 1319117 Rnaseh1 ribonuclease H1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:12667461 1319119 Son Son DNA binding protein gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0000248 macrocytosis IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0000433 microcephaly IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0001258 decreased body length IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0001399 hyperactivity IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0002083 premature death IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0003604 single kidney IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1319119 Son Son DNA binding protein gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0008184 abnormal naive B cell morphology IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0008188 abnormal transitional stage B cell morphology IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0009922 increased transitional stage T1 B cell number IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0011246 abnormal fetal liver hematopoietic progenitor cell morphology IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0013660 abnormal bone marrow hematopoietic cell morphology IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0013704 increased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319119 Son Son DNA binding protein gene MP:0021182 decreased femoral compact bone area IAGP N RGD:5509061 20240530 MGI PMID:38290089 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220811 MGI PMID:34897408 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0001925 male infertility IAGP N RGD:5509061 20220106 MGI PMID:34445597 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0001925 male infertility IAGP N RGD:5509061 20220811 MGI PMID:34897408 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220811 MGI PMID:34897408 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220811 MGI PMID:34897408 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220106 MGI PMID:34445597 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220811 MGI PMID:34897408 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220811 MGI PMID:34897408 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20220106 MGI PMID:34445597 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220811 MGI PMID:34897408 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220811 MGI PMID:34897408 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220811 MGI PMID:34897408 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220106 MGI PMID:34445597 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220811 MGI PMID:34897408 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220106 MGI PMID:34445597 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220106 MGI PMID:34445597 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220106 MGI PMID:34445597 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220811 MGI PMID:34897408 1319120 Zdhhc19 zinc finger, DHHC domain containing 19 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220811 MGI PMID:34897408 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0000075 absent neurocranium IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20200514 MGI 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0003104 acrania IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0004383 absent interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0004443 absent supraoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0004459 small alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20160922 MGI PMID:24833801 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20160922 MGI PMID:24833801 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20160922 MGI PMID:24833801 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0012686 everted embryonic neuroepithelium IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0012702 increased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0012705 increased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20171005 MGI PMID:18303018 1319122 Scube1 signal peptide, CUB domain, EGF-like 1 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:24833801 1319126 Eif3b eukaryotic translation initiation factor 3, subunit B gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20150611 MGI PMID:12038979 1319132 Bco2 beta-carotene oxygenase 2 gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:21106934 1319132 Bco2 beta-carotene oxygenase 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20962153 1319132 Bco2 beta-carotene oxygenase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20962153 1319132 Bco2 beta-carotene oxygenase 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20962153 1319132 Bco2 beta-carotene oxygenase 2 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20962153 1319132 Bco2 beta-carotene oxygenase 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:20962153 1319132 Bco2 beta-carotene oxygenase 2 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:20962153 1319132 Bco2 beta-carotene oxygenase 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:20962153 1319132 Bco2 beta-carotene oxygenase 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21106934 1319132 Bco2 beta-carotene oxygenase 2 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20962153 1319132 Bco2 beta-carotene oxygenase 2 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21106934 1319132 Bco2 beta-carotene oxygenase 2 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:21106934 1319132 Bco2 beta-carotene oxygenase 2 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21106934 1319134 Mex3c mex3 RNA binding family member C gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22357625 1319134 Mex3c mex3 RNA binding family member C gene MP:0001265 decreased body size IAGP N RGD:5509061 20150205 MGI PMID:24706898 1319134 Mex3c mex3 RNA binding family member C gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:22357625 1319134 Mex3c mex3 RNA binding family member C gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22357625 1319134 Mex3c mex3 RNA binding family member C gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:22357625 1319134 Mex3c mex3 RNA binding family member C gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:22357625 1319134 Mex3c mex3 RNA binding family member C gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20150205 MGI PMID:24706898 1319134 Mex3c mex3 RNA binding family member C gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22357625 1319134 Mex3c mex3 RNA binding family member C gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:22357625 1319134 Mex3c mex3 RNA binding family member C gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:22357625 1319134 Mex3c mex3 RNA binding family member C gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:22357625 1319134 Mex3c mex3 RNA binding family member C gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:22357625 1319134 Mex3c mex3 RNA binding family member C gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20150205 MGI PMID:24706898 1319134 Mex3c mex3 RNA binding family member C gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20150205 MGI PMID:24706898 1319134 Mex3c mex3 RNA binding family member C gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20150205 MGI PMID:24706898 1319134 Mex3c mex3 RNA binding family member C gene MP:0008831 abnormal insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:22357625 1319134 Mex3c mex3 RNA binding family member C gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22357625 1319143 Tomm34 translocase of outer mitochondrial membrane 34 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12801914 1319152 1700008O03Rik RIKEN cDNA 1700008O03 gene gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20201022 MGI 1319152 1700008O03Rik RIKEN cDNA 1700008O03 gene gene MP:0002608 increased hematocrit IEA N RGD:5509061 20201022 MGI 1319157 Ptch1 patched 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:8830098 1319157 Ptch1 patched 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:16936073 1319157 Ptch1 patched 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9262482 1319157 Ptch1 patched 1 gene MP:0000373 belly spot IEA N RGD:5509061 20111116 MGI 1319157 Ptch1 patched 1 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:12648487 1319157 Ptch1 patched 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:12872247 1319157 Ptch1 patched 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23055936 1319157 Ptch1 patched 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:12372258 1319157 Ptch1 patched 1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:22698544 1319157 Ptch1 patched 1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0000435 shortened head IEA N RGD:5509061 20111116 MGI 1319157 Ptch1 patched 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16936073 1319157 Ptch1 patched 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12917290 1319157 Ptch1 patched 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:16849540 1319157 Ptch1 patched 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9262482 1319157 Ptch1 patched 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:9262482 1319157 Ptch1 patched 1 gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20141003 MGI PMID:8830098 1319157 Ptch1 patched 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0000588 thick tail IAGP N RGD:5509061 20141003 MGI PMID:8830098 1319157 Ptch1 patched 1 gene MP:0000592 short tail IEA N RGD:5509061 20111116 MGI 1319157 Ptch1 patched 1 gene MP:0000753 paralysis IAGP N RGD:5509061 20160804 MGI PMID:24141783 1319157 Ptch1 patched 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15576403 1319157 Ptch1 patched 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319157 Ptch1 patched 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:18691548 1319157 Ptch1 patched 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319157 Ptch1 patched 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319157 Ptch1 patched 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18691548 1319157 Ptch1 patched 1 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:19147535 1319157 Ptch1 patched 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:12361967 1319157 Ptch1 patched 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12361967 1319157 Ptch1 patched 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15576403 1319157 Ptch1 patched 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22698544 1319157 Ptch1 patched 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:15576403 1319157 Ptch1 patched 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:12372258 1319157 Ptch1 patched 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:12872247 1319157 Ptch1 patched 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:19321799 1319157 Ptch1 patched 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:9262482 1319157 Ptch1 patched 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:12872247 1319157 Ptch1 patched 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:12361967 1319157 Ptch1 patched 1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:8830098 1319157 Ptch1 patched 1 gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:8830098 1319157 Ptch1 patched 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20171207 MGI PMID:23404854 1319157 Ptch1 patched 1 gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:9262482 1319157 Ptch1 patched 1 gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160804 MGI PMID:24141783 1319157 Ptch1 patched 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:15576403 1319157 Ptch1 patched 1 gene MP:0001300 ocular hypertelorism IEA N RGD:5509061 20111116 MGI 1319157 Ptch1 patched 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19213072 1319157 Ptch1 patched 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11668681 1319157 Ptch1 patched 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319157 Ptch1 patched 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22698544 1319157 Ptch1 patched 1 gene MP:0001699 increased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15576403 1319157 Ptch1 patched 1 gene MP:0001699 increased embryo size IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12872247 1319157 Ptch1 patched 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20171207 MGI PMID:23404854 1319157 Ptch1 patched 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20171207 MGI PMID:23404854 1319157 Ptch1 patched 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:19147535 1319157 Ptch1 patched 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200611 MGI PMID:30452905 1319157 Ptch1 patched 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:12648487 1319157 Ptch1 patched 1 gene MP:0001924 infertility IAGP N RGD:5509061 20171207 MGI PMID:23404854 1319157 Ptch1 patched 1 gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 1319157 Ptch1 patched 1 gene MP:0001926 female infertility IEA N RGD:5509061 20111116 MGI 1319157 Ptch1 patched 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16849540 1319157 Ptch1 patched 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19147535 1319157 Ptch1 patched 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19321799 1319157 Ptch1 patched 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22792366 1319157 Ptch1 patched 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9262482 1319157 Ptch1 patched 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200611 MGI PMID:30452905 1319157 Ptch1 patched 1 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15475264 1319157 Ptch1 patched 1 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16849540 1319157 Ptch1 patched 1 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17047082 1319157 Ptch1 patched 1 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17452975 1319157 Ptch1 patched 1 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19147535 1319157 Ptch1 patched 1 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19321799 1319157 Ptch1 patched 1 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12872247 1319157 Ptch1 patched 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22792366 1319157 Ptch1 patched 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16849540 1319157 Ptch1 patched 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17452975 1319157 Ptch1 patched 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18691548 1319157 Ptch1 patched 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19147535 1319157 Ptch1 patched 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19321799 1319157 Ptch1 patched 1 gene MP:0002083 premature death IAGP N RGD:5509061 20160804 MGI PMID:24141783 1319157 Ptch1 patched 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:22792366 1319157 Ptch1 patched 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12372258 1319157 Ptch1 patched 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15576403 1319157 Ptch1 patched 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19666503 1319157 Ptch1 patched 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22549777 1319157 Ptch1 patched 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12872247 1319157 Ptch1 patched 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15269168 1319157 Ptch1 patched 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18272593 1319157 Ptch1 patched 1 gene MP:0002271 abnormal pulmonary alveolar duct morphology IAGP N RGD:5509061 20141003 MGI PMID:15576403 1319157 Ptch1 patched 1 gene MP:0002286 cryptorchism IEA N RGD:5509061 20111116 MGI 1319157 Ptch1 patched 1 gene MP:0002367 abnormal thymus lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:20018657 1319157 Ptch1 patched 1 gene MP:0002716 small male preputial gland IAGP N RGD:5509061 20141003 MGI PMID:8830098 1319157 Ptch1 patched 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16936073 1319157 Ptch1 patched 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:15576403 1319157 Ptch1 patched 1 gene MP:0003190 fused synovial joints IAGP N RGD:5509061 20141003 MGI PMID:16936073 1319157 Ptch1 patched 1 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:19321799 1319157 Ptch1 patched 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16936073 1319157 Ptch1 patched 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20233865 1319157 Ptch1 patched 1 gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:8830098 1319157 Ptch1 patched 1 gene MP:0003580 increased fibroma incidence IAGP N RGD:5509061 20141003 MGI PMID:19321799 1319157 Ptch1 patched 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:12917290 1319157 Ptch1 patched 1 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19147535 1319157 Ptch1 patched 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:22792366 1319157 Ptch1 patched 1 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:22698544 1319157 Ptch1 patched 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20160804 MGI PMID:24141783 1319157 Ptch1 patched 1 gene MP:0003841 abnormal lambdoid suture morphology IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:12917290 1319157 Ptch1 patched 1 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12386820 1319157 Ptch1 patched 1 gene MP:0004175 telangiectasia IAGP N RGD:5509061 20141003 MGI PMID:16849540 1319157 Ptch1 patched 1 gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20141003 MGI PMID:22792366 1319157 Ptch1 patched 1 gene MP:0004199 increased fetal size IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0004199 increased fetal size IAGP N RGD:5509061 20141003 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16849540 1319157 Ptch1 patched 1 gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19321799 1319157 Ptch1 patched 1 gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20233865 1319157 Ptch1 patched 1 gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20171207 MGI PMID:23404854 1319157 Ptch1 patched 1 gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20181220 MGI PMID:10545995 1319157 Ptch1 patched 1 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0004342 scapular bone foramen IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0004460 alisphenoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0004478 increased testicular teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16849540 1319157 Ptch1 patched 1 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:12386820 1319157 Ptch1 patched 1 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20180621 MGI PMID:21351254 1319157 Ptch1 patched 1 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20181220 MGI PMID:10545995 1319157 Ptch1 patched 1 gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20181220 MGI PMID:10545995 1319157 Ptch1 patched 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:16936073 1319157 Ptch1 patched 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20171207 MGI PMID:23404854 1319157 Ptch1 patched 1 gene MP:0004733 abnormal thoracic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:8830098 1319157 Ptch1 patched 1 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:22792366 1319157 Ptch1 patched 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:18691548 1319157 Ptch1 patched 1 gene MP:0004971 dermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8830098 1319157 Ptch1 patched 1 gene MP:0004979 abnormal neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:15576403 1319157 Ptch1 patched 1 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:15576403 1319157 Ptch1 patched 1 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:18691548 1319157 Ptch1 patched 1 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:22869526 1319157 Ptch1 patched 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:11668681 1319157 Ptch1 patched 1 gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:12361967 1319157 Ptch1 patched 1 gene MP:0005503 abnormal tendon morphology IEA N RGD:5509061 20111116 MGI 1319157 Ptch1 patched 1 gene MP:0005508 abnormal skeleton morphology IEA N RGD:5509061 20111116 MGI 1319157 Ptch1 patched 1 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12386820 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16260494 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16849540 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17047082 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17452975 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18691548 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19147535 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19164512 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19185848 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19213072 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19321799 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22343890 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9262482 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20180621 MGI PMID:21351254 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20200611 MGI PMID:30452905 1319157 Ptch1 patched 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20240404 MGI PMID:38517960 1319157 Ptch1 patched 1 gene MP:0006292 abnormal nasal placode morphology IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0006294 absent optic vesicle IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0006322 abnormal perichondrium morphology IAGP N RGD:5509061 20171221 MGI PMID:16936073 1319157 Ptch1 patched 1 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15576403 1319157 Ptch1 patched 1 gene MP:0006343 enlarged first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15576403 1319157 Ptch1 patched 1 gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 1319157 Ptch1 patched 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16936073 1319157 Ptch1 patched 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20160804 MGI PMID:24141783 1319157 Ptch1 patched 1 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:16936073 1319157 Ptch1 patched 1 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20210114 MGI PMID:32702291 1319157 Ptch1 patched 1 gene MP:0008785 abnormal sternum manubrium morphology IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0008914 enlarged cerebellum IAGP N RGD:5509061 20141003 MGI PMID:18691548 1319157 Ptch1 patched 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20200611 MGI PMID:30452905 1319157 Ptch1 patched 1 gene MP:0009882 absent palatal shelf IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16260494 1319157 Ptch1 patched 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19147535 1319157 Ptch1 patched 1 gene MP:0010283 decreased classified tumor incidence IAGP N RGD:5509061 20240404 MGI PMID:38517960 1319157 Ptch1 patched 1 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12648487 1319157 Ptch1 patched 1 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:16849540 1319157 Ptch1 patched 1 gene MP:0010642 absent third pharyngeal arch IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0010643 absent fourth pharyngeal arch IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0010939 abnormal mandibular prominence morphology IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12372258 1319157 Ptch1 patched 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12917290 1319157 Ptch1 patched 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21406566 1319157 Ptch1 patched 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9262482 1319157 Ptch1 patched 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11668681 1319157 Ptch1 patched 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12361967 1319157 Ptch1 patched 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16061793 1319157 Ptch1 patched 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19321799 1319157 Ptch1 patched 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19666503 1319157 Ptch1 patched 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20171214 MGI PMID:21305688 1319157 Ptch1 patched 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16936073 1319157 Ptch1 patched 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15576403 1319157 Ptch1 patched 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0011712 arrested osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:16936073 1319157 Ptch1 patched 1 gene MP:0011934 abnormal branching involved in pancreas development IAGP N RGD:5509061 20141218 MGI PMID:12917290 1319157 Ptch1 patched 1 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:12872247 1319157 Ptch1 patched 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19147535 1319157 Ptch1 patched 1 gene MP:0012525 abnormal rhombic lip morphology IAGP N RGD:5509061 20141003 MGI PMID:18691548 1319157 Ptch1 patched 1 gene MP:0012675 enlarged floor plate IAGP N RGD:5509061 20141003 MGI PMID:15576403 1319157 Ptch1 patched 1 gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20210114 MGI PMID:32702291 1319157 Ptch1 patched 1 gene MP:0013551 decreased cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20200611 MGI PMID:30452905 1319157 Ptch1 patched 1 gene MP:0013945 abnormal elbow joint morphology IAGP N RGD:5509061 20171221 MGI PMID:16936073 1319157 Ptch1 patched 1 gene MP:0014100 increased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:16936073 1319157 Ptch1 patched 1 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20240404 MGI PMID:38517960 1319157 Ptch1 patched 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:19147535 1319157 Ptch1 patched 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:16936073 1319157 Ptch1 patched 1 gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:12361967 1319157 Ptch1 patched 1 gene MP:0021217 abnormal palatal shelf bone ossification IAGP N RGD:5509061 20230223 MGI PMID:21364421 1319157 Ptch1 patched 1 gene MP:0030137 abnormal upper incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:20018657 1319157 Ptch1 patched 1 gene MP:0030220 mandibular cyst IAGP N RGD:5509061 20171019 MGI PMID:12542834 1319157 Ptch1 patched 1 gene MP:0030220 mandibular cyst IAGP N RGD:5509061 20171019 MGI PMID:9585239 1319157 Ptch1 patched 1 gene MP:0030284 short mandibular coronoid process IAGP N RGD:5509061 20171102 MGI PMID:23897749 1319157 Ptch1 patched 1 gene MP:0030285 mandibular coronoid process hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:23897749 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20211118 MGI PMID:27875292 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20211118 MGI PMID:27875292 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20181227 MGI 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20181227 MGI 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20211118 MGI PMID:27875292 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20211118 MGI PMID:27875292 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20211118 MGI PMID:27875292 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20211118 MGI PMID:27875292 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20211118 MGI PMID:27875292 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20211118 MGI PMID:27875292 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20211118 MGI PMID:27875292 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0011987 abnormal GABAergic neuron physiology IAGP N RGD:5509061 20211118 MGI PMID:27875292 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:27875292 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:27875292 1319161 Zdhhc3 zinc finger, DHHC domain containing 3 gene MP:0020358 abnormal inhibitory synapse morphology IAGP N RGD:5509061 20211118 MGI PMID:27875292 1319163 Bnc1 basonuclin zinc finger protein 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1319163 Bnc1 basonuclin zinc finger protein 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1319163 Bnc1 basonuclin zinc finger protein 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20210128 MGI 1319163 Bnc1 basonuclin zinc finger protein 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1319163 Bnc1 basonuclin zinc finger protein 1 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1319163 Bnc1 basonuclin zinc finger protein 1 gene MP:0001926 female infertility IEA N RGD:5509061 20230601 MGI 1319163 Bnc1 basonuclin zinc finger protein 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1319163 Bnc1 basonuclin zinc finger protein 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 1319163 Bnc1 basonuclin zinc finger protein 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1319163 Bnc1 basonuclin zinc finger protein 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20240523 MGI 1319163 Bnc1 basonuclin zinc finger protein 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230601 MGI 1319163 Bnc1 basonuclin zinc finger protein 1 gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:17971852 1319163 Bnc1 basonuclin zinc finger protein 1 gene MP:0020858 cornea epithelium hypoplasia IAGP N RGD:5509061 20181101 MGI PMID:17971852 1319163 Bnc1 basonuclin zinc finger protein 1 gene MP:0020861 abnormal cornea wound healing IAGP N RGD:5509061 20181101 MGI PMID:17971852 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15312245 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:15312245 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:9506940 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12514218 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:12514218 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12514218 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:9506940 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:9506940 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9506940 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15312245 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12514218 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12514218 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20210128 MGI 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15312245 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210128 MGI 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15312245 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9990068 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0002774 small prostate gland IAGP N RGD:5509061 20141003 MGI PMID:9506940 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:15312245 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:15312245 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:15312245 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:12576486 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:17045797 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:9506940 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:15312245 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0005119 decreased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12576486 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10202153 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12576486 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:15312245 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:10202153 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:10202153 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0005474 increased triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:10202153 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:12576486 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:12576486 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15312245 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15312245 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20231207 MGI 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20181227 MGI 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20220915 MGI PMID:15312245 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:15312245 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1319168 Ncoa1 nuclear receptor coactivator 1 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:15312245 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0003939 abnormal myotome morphology IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0004444 small supraoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0004677 truncated ribs IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319170 Dmrt2 doublesex and mab-3 related transcription factor 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16387292 1319172 Snapc4 small nuclear RNA activating complex, polypeptide 4 gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20160804 MGI 1319177 Dpf3 double PHD fingers 3 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1319177 Dpf3 double PHD fingers 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210826 MGI 1319177 Dpf3 double PHD fingers 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1319177 Dpf3 double PHD fingers 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 1319177 Dpf3 double PHD fingers 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1319177 Dpf3 double PHD fingers 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20220519 MGI PMID:31848143 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0000161 scoliosis IAGP N RGD:5509061 20220519 MGI PMID:31848143 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20220519 MGI PMID:31848143 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220519 MGI PMID:31848143 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20220519 MGI PMID:31848143 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20220519 MGI PMID:31848143 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20220519 MGI PMID:31848143 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0005227 abnormal vertebral body development IAGP N RGD:5509061 20220519 MGI PMID:31848143 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20220519 MGI PMID:31848143 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20220519 MGI PMID:31848143 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20220519 MGI PMID:31848143 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21159818 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20220519 MGI PMID:31848143 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:21159818 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0014561 decreased cortical ventricular zone cell density IAGP N RGD:5509061 20241031 MGI PMID:24013503 1319179 Prmt5 protein arginine N-methyltransferase 5 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20220519 MGI PMID:31848143 1319180 Tcf25 transcription factor 25 (basic helix-loop-helix) gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1319180 Tcf25 transcription factor 25 (basic helix-loop-helix) gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1319180 Tcf25 transcription factor 25 (basic helix-loop-helix) gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1319180 Tcf25 transcription factor 25 (basic helix-loop-helix) gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1319180 Tcf25 transcription factor 25 (basic helix-loop-helix) gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210128 MGI 1319180 Tcf25 transcription factor 25 (basic helix-loop-helix) gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20240530 MGI PMID:32805187 1319180 Tcf25 transcription factor 25 (basic helix-loop-helix) gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20240523 MGI 1319180 Tcf25 transcription factor 25 (basic helix-loop-helix) gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1319182 Ngef neuronal guanine nucleotide exchange factor gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20170209 MGI PMID:15848799 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0000199 abnormal circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:17053834 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16713561 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17053834 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20141003 MGI PMID:21804564 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:17053834 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:19412431 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:19412431 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17053834 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19412431 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:19412431 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16713561 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17053834 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:17053834 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19412431 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17053834 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:16713561 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17053834 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16501569 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19412431 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:19412431 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20141003 MGI PMID:19412431 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17723219 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:21804564 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0003282 gastric ulcer IAGP N RGD:5509061 20141003 MGI PMID:17053834 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:19412431 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17053834 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16501569 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16501569 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:16501569 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16501569 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16501569 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0008136 enlarged Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:17923499 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:17053834 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20141003 MGI PMID:21804564 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0009582 abnormal keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16713561 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16713561 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19412431 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17723219 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19412431 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:19412431 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0011707 impaired fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:19412431 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20150219 MGI PMID:24557836 1319184 Cyld CYLD lysine 63 deubiquitinase gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20150312 MGI PMID:21804564 1319186 Tbx4 T-box 4 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:12736212 1319186 Tbx4 T-box 4 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:12736212 1319186 Tbx4 T-box 4 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:20152185 1319186 Tbx4 T-box 4 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1319186 Tbx4 T-box 4 gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1319186 Tbx4 T-box 4 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:12736212 1319186 Tbx4 T-box 4 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:12736212 1319186 Tbx4 T-box 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12736212 1319186 Tbx4 T-box 4 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21932311 1319186 Tbx4 T-box 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23328398 1319186 Tbx4 T-box 4 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:18579682 1319186 Tbx4 T-box 4 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:18579682 1319186 Tbx4 T-box 4 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:18579682 1319186 Tbx4 T-box 4 gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:18579682 1319186 Tbx4 T-box 4 gene MP:0003230 abnormal umbilical artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12736212 1319186 Tbx4 T-box 4 gene MP:0003891 increased allantois apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12736212 1319186 Tbx4 T-box 4 gene MP:0004349 absent femur IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0004507 abnormal ischium morphology IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18579682 1319186 Tbx4 T-box 4 gene MP:0004558 delayed allantois development IAGP N RGD:5509061 20141003 MGI PMID:12736212 1319186 Tbx4 T-box 4 gene MP:0004559 small allantois IAGP N RGD:5509061 20141003 MGI PMID:12736212 1319186 Tbx4 T-box 4 gene MP:0005353 abnormal patella morphology IAGP N RGD:5509061 20141003 MGI PMID:18579682 1319186 Tbx4 T-box 4 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:18579682 1319186 Tbx4 T-box 4 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:20152185 1319186 Tbx4 T-box 4 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0008919 fused tarsal bones IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0008919 fused tarsal bones IAGP N RGD:5509061 20141003 MGI PMID:18579682 1319186 Tbx4 T-box 4 gene MP:0009656 delayed chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12736212 1319186 Tbx4 T-box 4 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12736212 1319186 Tbx4 T-box 4 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12736212 1319186 Tbx4 T-box 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170105 MGI 1319186 Tbx4 T-box 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0012134 absent umbilical cord IAGP N RGD:5509061 20141003 MGI PMID:12736212 1319186 Tbx4 T-box 4 gene MP:0013169 small hindlimb buds IAGP N RGD:5509061 20141003 MGI PMID:12736212 1319186 Tbx4 T-box 4 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1319186 Tbx4 T-box 4 gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:17164415 1319186 Tbx4 T-box 4 gene MP:0030860 patellar dislocation IAGP N RGD:5509061 20181025 MGI PMID:18579682 1319188 Fam161b family with sequence similarity 161, member B gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220519 MGI 1319188 Fam161b family with sequence similarity 161, member B gene MP:0000274 enlarged heart IEA N RGD:5509061 20220519 MGI 1319188 Fam161b family with sequence similarity 161, member B gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1319188 Fam161b family with sequence similarity 161, member B gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1319188 Fam161b family with sequence similarity 161, member B gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1319188 Fam161b family with sequence similarity 161, member B gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220519 MGI 1319188 Fam161b family with sequence similarity 161, member B gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220519 MGI 1319188 Fam161b family with sequence similarity 161, member B gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230601 MGI 1319188 Fam161b family with sequence similarity 161, member B gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1319190 Irx1 Iroquois homeobox 1 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20181227 MGI 1319190 Irx1 Iroquois homeobox 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1319190 Irx1 Iroquois homeobox 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1319190 Irx1 Iroquois homeobox 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0003257 abnormal abdominal wall morphology IEA N RGD:5509061 20181227 MGI 1319190 Irx1 Iroquois homeobox 1 gene MP:0003641 small lung IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1319190 Irx1 Iroquois homeobox 1 gene MP:0005359 growth retardation of incisors IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20240523 MGI 1319190 Irx1 Iroquois homeobox 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319190 Irx1 Iroquois homeobox 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1319190 Irx1 Iroquois homeobox 1 gene MP:0030080 small lower incisors IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0030089 short lower incisors IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0030453 abnormal odontoblast morphology IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0030471 abnormal ameloblast differentiation IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0030508 abnormal dental epithelium morphology IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0030518 abnormal outer dental epithelium morphology IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319190 Irx1 Iroquois homeobox 1 gene MP:0030523 abnormal stratum intermedium morphology IAGP N RGD:5509061 20180621 MGI PMID:28746823 1319192 Neurog2 neurogenin 2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:10640277 1319192 Neurog2 neurogenin 2 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:18448566 1319192 Neurog2 neurogenin 2 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:10640277 1319192 Neurog2 neurogenin 2 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18448566 1319192 Neurog2 neurogenin 2 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:10640277 1319192 Neurog2 neurogenin 2 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20133851 1319192 Neurog2 neurogenin 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20151112 MGI PMID:18400164 1319192 Neurog2 neurogenin 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11825874 1319192 Neurog2 neurogenin 2 gene MP:0001034 abnormal parasympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20133851 1319192 Neurog2 neurogenin 2 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20133851 1319192 Neurog2 neurogenin 2 gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9539123 1319192 Neurog2 neurogenin 2 gene MP:0001084 abnormal petrosal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9539123 1319192 Neurog2 neurogenin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9539123 1319192 Neurog2 neurogenin 2 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9539123 1319192 Neurog2 neurogenin 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9539123 1319192 Neurog2 neurogenin 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9539123 1319192 Neurog2 neurogenin 2 gene MP:0002751 abnormal autonomic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:20133851 1319192 Neurog2 neurogenin 2 gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:20133851 1319192 Neurog2 neurogenin 2 gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18448566 1319192 Neurog2 neurogenin 2 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:9539123 1319192 Neurog2 neurogenin 2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:18448566 1319192 Neurog2 neurogenin 2 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:18448566 1319192 Neurog2 neurogenin 2 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:16705040 1319192 Neurog2 neurogenin 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:18448566 1319192 Neurog2 neurogenin 2 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0008031 decreased Cajal-Retzius cell number IAGP N RGD:5509061 20141003 MGI PMID:18579678 1319192 Neurog2 neurogenin 2 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:10640277 1319192 Neurog2 neurogenin 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16705040 1319192 Neurog2 neurogenin 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18448566 1319192 Neurog2 neurogenin 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9539123 1319192 Neurog2 neurogenin 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18448566 1319192 Neurog2 neurogenin 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9539123 1319192 Neurog2 neurogenin 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10640277 1319192 Neurog2 neurogenin 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15105417 1319192 Neurog2 neurogenin 2 gene MP:0021091 abnormal dorsal interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:15901662 1319192 Neurog2 neurogenin 2 gene MP:0021093 abnormal dorsal interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:15901662 1319192 Neurog2 neurogenin 2 gene MP:0021094 abnormal dorsal interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:15901662 1319192 Neurog2 neurogenin 2 gene MP:0021095 abnormal dorsal interneuron 4 morphology IAGP N RGD:5509061 20220310 MGI PMID:15901662 1319192 Neurog2 neurogenin 2 gene MP:0021096 abnormal dorsal interneuron 5 morphology IAGP N RGD:5509061 20220310 MGI PMID:15901662 1319192 Neurog2 neurogenin 2 gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:18400164 1319192 Neurog2 neurogenin 2 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:15105417 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9492006 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:11371356 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:22588720 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12091879 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:12091879 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:12151598 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:18441309 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:9834104 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18441309 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:18441309 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11371356 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:11086031 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:12151598 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001573 abnormal circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:12960353 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11371356 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:18441309 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:12441072 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12441072 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12441072 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:11371356 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:18441309 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11371356 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:18441309 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:10486156 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:19147789 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11371356 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:12091879 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:12091879 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:11086031 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12091879 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002334 abnormal airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:11839568 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002334 abnormal airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:9500796 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:12091879 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11839568 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12960353 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8602264 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:12960353 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9500796 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11839568 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12151598 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:18719110 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:8602263 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:8624821 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:9500796 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:9834104 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:8602263 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:8602263 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:9492006 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:12960353 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12709397 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:9500796 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16200068 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16275384 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:11839568 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:11371356 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:22101429 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0004481 abnormal conjunctival epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18441309 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:15721841 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:15721841 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:8602264 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0004881 abnormal lung size IAGP N RGD:5509061 20141003 MGI PMID:12091879 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:18441309 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17873878 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16275384 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15213110 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9492006 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:8602264 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11086031 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8602263 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8602263 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8624821 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8602264 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:18441309 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22101429 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:8602263 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:17611223 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:22588720 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23727894 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8602264 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9834104 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008091 decreased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:21460847 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18719110 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8602264 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8624821 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12151598 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:8602263 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9500796 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9834104 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:12441072 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9492006 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9500796 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9834104 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:12960353 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12441072 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15721841 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9834104 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:8624821 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:16275384 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20141003 MGI PMID:9500796 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008601 abnormal circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:9500796 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008625 abnormal circulating interleukin-5 level IAGP N RGD:5509061 20141003 MGI PMID:9500796 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:12151598 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:9834104 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:12441072 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:10486156 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:12441072 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15721841 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:8624821 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:8624821 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12960353 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18719110 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:9500796 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008724 impaired eosinophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12960353 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19147789 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22588720 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0010064 increased circulating creatine level IAGP N RGD:5509061 20141003 MGI PMID:12709397 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22588720 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0010942 abnormal respiratory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11839568 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0010942 abnormal respiratory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9500796 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:22101429 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16275384 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:12441072 1319195 Stat6 signal transducer and activator of transcription 6 gene MP:0030757 abnormal circulating histamine level IAGP N RGD:5509061 20180927 MGI PMID:12151598 1319199 Adam24 ADAM metallopeptidase domain 24 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:19670298 1319199 Adam24 ADAM metallopeptidase domain 24 gene MP:0031014 polyspermy IAGP N RGD:5509061 20200130 MGI PMID:19670298 1319202 Adprs ADP-ribosylserine hydrolase gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20220519 MGI 1319202 Adprs ADP-ribosylserine hydrolase gene MP:0001257 increased body length IEA N RGD:5509061 20220519 MGI 1319202 Adprs ADP-ribosylserine hydrolase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 1319202 Adprs ADP-ribosylserine hydrolase gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20201001 MGI PMID:30830864 1319202 Adprs ADP-ribosylserine hydrolase gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220519 MGI 1319202 Adprs ADP-ribosylserine hydrolase gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220519 MGI 1319202 Adprs ADP-ribosylserine hydrolase gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1319202 Adprs ADP-ribosylserine hydrolase gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20201001 MGI PMID:30830864 1319204 Fyco1 FYVE and coiled-coil domain containing 1 gene MP:0001304 cataract IAGP N RGD:5509061 20231012 MGI PMID:35343376 1319204 Fyco1 FYVE and coiled-coil domain containing 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1319204 Fyco1 FYVE and coiled-coil domain containing 1 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20231012 MGI PMID:35343376 1319204 Fyco1 FYVE and coiled-coil domain containing 1 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20231012 MGI PMID:35343376 1319204 Fyco1 FYVE and coiled-coil domain containing 1 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20231012 MGI PMID:35343376 1319204 Fyco1 FYVE and coiled-coil domain containing 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20231012 MGI PMID:35343376 1319204 Fyco1 FYVE and coiled-coil domain containing 1 gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20231012 MGI PMID:35343376 1319204 Fyco1 FYVE and coiled-coil domain containing 1 gene MP:0013732 mature cataract IAGP N RGD:5509061 20231012 MGI PMID:35343376 1319204 Fyco1 FYVE and coiled-coil domain containing 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1319204 Fyco1 FYVE and coiled-coil domain containing 1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20231012 MGI PMID:35343376 1319206 Ctsa cathepsin A gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20221215 MGI 1319206 Ctsa cathepsin A gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20221215 MGI 1319206 Ctsa cathepsin A gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0000550 abnormal forelimb morphology IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:7590240 1319206 Ctsa cathepsin A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7590240 1319206 Ctsa cathepsin A gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:7590240 1319206 Ctsa cathepsin A gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:18391110 1319206 Ctsa cathepsin A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7590240 1319206 Ctsa cathepsin A gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:7590240 1319206 Ctsa cathepsin A gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0001406 abnormal gait IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:7590240 1319206 Ctsa cathepsin A gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:18391110 1319206 Ctsa cathepsin A gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:7590240 1319206 Ctsa cathepsin A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7590240 1319206 Ctsa cathepsin A gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20221215 MGI 1319206 Ctsa cathepsin A gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1319206 Ctsa cathepsin A gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20221215 MGI 1319206 Ctsa cathepsin A gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20221215 MGI 1319206 Ctsa cathepsin A gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18391110 1319206 Ctsa cathepsin A gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18391110 1319206 Ctsa cathepsin A gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18391110 1319206 Ctsa cathepsin A gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:7590240 1319206 Ctsa cathepsin A gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20221215 MGI 1319206 Ctsa cathepsin A gene MP:0005287 narrow eye opening IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0005333 decreased heart rate IEA N RGD:5509061 20230601 MGI 1319206 Ctsa cathepsin A gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20221215 MGI 1319206 Ctsa cathepsin A gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20221215 MGI 1319206 Ctsa cathepsin A gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20221215 MGI 1319206 Ctsa cathepsin A gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20221215 MGI 1319206 Ctsa cathepsin A gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20221215 MGI 1319206 Ctsa cathepsin A gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20240523 MGI 1319206 Ctsa cathepsin A gene MP:0006083 abnormal blood vessel elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18391110 1319206 Ctsa cathepsin A gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18391110 1319206 Ctsa cathepsin A gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18391110 1319206 Ctsa cathepsin A gene MP:0008418 abnormal cutaneous elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18391110 1319206 Ctsa cathepsin A gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20221215 MGI 1319206 Ctsa cathepsin A gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 1319206 Ctsa cathepsin A gene MP:0009456 impaired cued conditioning behavior IEA N RGD:5509061 20230601 MGI 1319206 Ctsa cathepsin A gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20230601 MGI 1319206 Ctsa cathepsin A gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:18391110 1319206 Ctsa cathepsin A gene MP:0012175 flat face IAGP N RGD:5509061 20171109 MGI PMID:7590240 1319206 Ctsa cathepsin A gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20230601 MGI 1319206 Ctsa cathepsin A gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18342849 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18342849 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11564878 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:18342849 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0001925 male infertility IAGP N RGD:5509061 20220428 MGI PMID:18342849 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18342849 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:18342849 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:15056615 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15056615 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:15056615 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:18342849 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0002673 abnormal sperm number IAGP N RGD:5509061 20141003 MGI PMID:18342849 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18342849 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18342849 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0002785 absent Leydig cells IAGP N RGD:5509061 20150319 MGI PMID:15056615 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20141003 MGI PMID:18342849 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18342849 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11564878 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20141003 MGI PMID:15056615 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0005652 sex reversal IAGP N RGD:5509061 20141003 MGI PMID:15056615 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:18342849 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18342849 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11564878 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18342849 1319209 Sox8 SRY (sex determining region Y)-box 8 gene MP:0031389 abnormal ectoplasmic specialization morphology IAGP N RGD:5509061 20220428 MGI PMID:18342849 1319210 Fbxo48 F-box protein 48 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1319210 Fbxo48 F-box protein 48 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16597604 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16287712 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14691480 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16170381 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16287712 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16287712 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:16287712 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:16287712 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16287712 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16287712 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14691480 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:14691480 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:16287712 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:14691480 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16287712 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14691480 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16287712 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16287712 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16287712 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:14691480 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:14691480 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:14691480 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:14691480 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:14691480 1319221 Gadd45b growth arrest and DNA-damage-inducible 45 beta gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:16287712 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0000022 abnormal ear shape IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0000097 short maxilla IAGP N RGD:5509061 20170406 MGI PMID:25273096 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0000111 cleft palate IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20160721 MGI PMID:26932671 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20160721 MGI PMID:26932671 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0000440 domed cranium IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0000447 flattened snout IAGP N RGD:5509061 20170921 MGI PMID:25273096 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20170406 MGI PMID:25273096 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001258 decreased body length IAGP N RGD:5509061 20210422 MGI PMID:33431871 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170406 MGI PMID:25273096 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210422 MGI PMID:25346535 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210422 MGI PMID:33431871 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001265 decreased body size IAGP N RGD:5509061 20210422 MGI PMID:33431871 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200730 MGI PMID:30891914 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200730 MGI PMID:30891914 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001407 short stride length IAGP N RGD:5509061 20200730 MGI PMID:30891914 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20200730 MGI PMID:30891914 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20170406 MGI PMID:25273096 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20200730 MGI PMID:30891914 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001513 limb grasping IAGP N RGD:5509061 20240215 MGI PMID:16972005 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001523 impaired righting response IAGP N RGD:5509061 20200730 MGI PMID:30891914 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20150122 MGI PMID:24368734 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001787 pericardial edema IAGP N RGD:5509061 20160721 MGI PMID:26932671 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0001953 respiratory failure IAGP N RGD:5509061 20150122 MGI PMID:24368734 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200730 MGI PMID:30891914 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0002083 premature death IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20150122 MGI PMID:24368734 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20200730 MGI PMID:30891914 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20160721 MGI PMID:26932671 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0002729 abnormal inner ear canal morphology IAGP N RGD:5509061 20170406 MGI PMID:25273096 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20210422 MGI PMID:25346535 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0003064 decreased coping response IAGP N RGD:5509061 20200730 MGI PMID:30891914 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160721 MGI PMID:26932671 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20160721 MGI PMID:26932671 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20150122 MGI PMID:24368734 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0004380 short frontal bone IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0004471 short nasal bone IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20210422 MGI PMID:25346535 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20210422 MGI PMID:25346535 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20200730 MGI PMID:30891914 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20210422 MGI PMID:33431871 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20210422 MGI PMID:25346535 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0006386 absent somites IAGP N RGD:5509061 20160721 MGI PMID:26932671 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0008285 abnormal hippocampus granule cell layer IAGP N RGD:5509061 20170406 MGI PMID:25273096 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20210422 MGI PMID:33431871 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0009317 increased follicular lymphoma incidence IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20170406 MGI PMID:25273096 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20150122 MGI PMID:24368734 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20160721 MGI PMID:26932671 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141016 MGI PMID:24368734 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160721 MGI PMID:26932671 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170406 MGI PMID:25273096 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0011170 abnormal brown fat cell differentiation IAGP N RGD:5509061 20150122 MGI PMID:24368734 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20240404 MGI PMID:26932671 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20160721 MGI PMID:26932671 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20210422 MGI PMID:33431871 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20160721 MGI PMID:26932671 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20170406 MGI PMID:25273096 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0012724 absent head fold IAGP N RGD:5509061 20160721 MGI PMID:26932671 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0012754 abnormal cranial neural crest cell morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20210422 MGI PMID:25346535 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20210422 MGI PMID:25346535 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0030065 face hypoplasia IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0030069 broad face IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0030259 mandibular condyloid process hypoplasia IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0030320 abnormal temporal bone tympanic part morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0030383 small presphenoid bone IAGP N RGD:5509061 20220915 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:30891914 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0031444 glossoptosis IAGP N RGD:5509061 20221027 MGI PMID:32541010 1319223 Kmt2d lysine (K)-specific methyltransferase 2D gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:32541010 1319229 Cd19 CD19 antigen gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:15908920 1319229 Cd19 CD19 antigen gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20170921 MGI PMID:26668357 1319229 Cd19 CD19 antigen gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11070163 1319229 Cd19 CD19 antigen gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20170314 MGI PMID:26301816 1319229 Cd19 CD19 antigen gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 1319229 Cd19 CD19 antigen gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11120817 1319229 Cd19 CD19 antigen gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:14668867 1319229 Cd19 CD19 antigen gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1319229 Cd19 CD19 antigen gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16782029 1319229 Cd19 CD19 antigen gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0000599 enlarged liver IAGP N RGD:5509061 20170314 MGI PMID:26301816 1319229 Cd19 CD19 antigen gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20170921 MGI PMID:26668357 1319229 Cd19 CD19 antigen gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20200402 MGI PMID:27135738 1319229 Cd19 CD19 antigen gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20231207 MGI PMID:32619424 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11509585 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12818163 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15148335 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17509906 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18663224 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20439541 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21300983 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21341261 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21844204 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23619366 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20150219 MGI PMID:24241423 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170314 MGI PMID:26301816 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170921 MGI PMID:26668357 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200402 MGI PMID:27135738 1319229 Cd19 CD19 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20220616 MGI PMID:33343574 1319229 Cd19 CD19 antigen gene MP:0000692 small spleen IAGP N RGD:5509061 20170824 MGI PMID:26443207 1319229 Cd19 CD19 antigen gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23619366 1319229 Cd19 CD19 antigen gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20170921 MGI PMID:26668357 1319229 Cd19 CD19 antigen gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16148088 1319229 Cd19 CD19 antigen gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20200402 MGI PMID:31921164 1319229 Cd19 CD19 antigen gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:18663224 1319229 Cd19 CD19 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12818163 1319229 Cd19 CD19 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15148335 1319229 Cd19 CD19 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18663224 1319229 Cd19 CD19 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21300983 1319229 Cd19 CD19 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20170314 MGI PMID:26301816 1319229 Cd19 CD19 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20170921 MGI PMID:26668357 1319229 Cd19 CD19 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200402 MGI PMID:27135738 1319229 Cd19 CD19 antigen gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15908920 1319229 Cd19 CD19 antigen gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:16507897 1319229 Cd19 CD19 antigen gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0001577 anemia IAGP N RGD:5509061 20170314 MGI PMID:26301816 1319229 Cd19 CD19 antigen gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:11509585 1319229 Cd19 CD19 antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:16862162 1319229 Cd19 CD19 antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12818163 1319229 Cd19 CD19 antigen gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14564011 1319229 Cd19 CD19 antigen gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14668867 1319229 Cd19 CD19 antigen gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20170314 MGI PMID:26301816 1319229 Cd19 CD19 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11420047 1319229 Cd19 CD19 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12707341 1319229 Cd19 CD19 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:14563324 1319229 Cd19 CD19 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:14715907 1319229 Cd19 CD19 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319229 Cd19 CD19 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:17000121 1319229 Cd19 CD19 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:19270713 1319229 Cd19 CD19 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319229 Cd19 CD19 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20210826 MGI PMID:33336366 1319229 Cd19 CD19 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20231102 MGI PMID:35439434 1319229 Cd19 CD19 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11509585 1319229 Cd19 CD19 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12707341 1319229 Cd19 CD19 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:14563324 1319229 Cd19 CD19 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16455962 1319229 Cd19 CD19 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:19270713 1319229 Cd19 CD19 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:7542548 1319229 Cd19 CD19 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:7543183 1319229 Cd19 CD19 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319229 Cd19 CD19 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319229 Cd19 CD19 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20210826 MGI PMID:33336366 1319229 Cd19 CD19 antigen gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11070163 1319229 Cd19 CD19 antigen gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11509585 1319229 Cd19 CD19 antigen gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:7542548 1319229 Cd19 CD19 antigen gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319229 Cd19 CD19 antigen gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20210826 MGI PMID:33336366 1319229 Cd19 CD19 antigen gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:20439541 1319229 Cd19 CD19 antigen gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20150219 MGI PMID:24241423 1319229 Cd19 CD19 antigen gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20060366 1319229 Cd19 CD19 antigen gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21930766 1319229 Cd19 CD19 antigen gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20170921 MGI PMID:26668357 1319229 Cd19 CD19 antigen gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20200402 MGI PMID:27135738 1319229 Cd19 CD19 antigen gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20439541 1319229 Cd19 CD19 antigen gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:12818163 1319229 Cd19 CD19 antigen gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:20060366 1319229 Cd19 CD19 antigen gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20200402 MGI PMID:27135738 1319229 Cd19 CD19 antigen gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20439541 1319229 Cd19 CD19 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21930766 1319229 Cd19 CD19 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22174151 1319229 Cd19 CD19 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20200402 MGI PMID:27135738 1319229 Cd19 CD19 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20231207 MGI PMID:32619424 1319229 Cd19 CD19 antigen gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:23023393 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11420047 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11967543 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14563324 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14668867 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15520246 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16166635 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20156974 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21124917 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21300983 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23023393 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7543183 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20200402 MGI PMID:31921164 1319229 Cd19 CD19 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20231207 MGI PMID:32619424 1319229 Cd19 CD19 antigen gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17244677 1319229 Cd19 CD19 antigen gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22589392 1319229 Cd19 CD19 antigen gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22666421 1319229 Cd19 CD19 antigen gene MP:0002221 abnormal lymph organ size IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20200402 MGI PMID:27135738 1319229 Cd19 CD19 antigen gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:11809737 1319229 Cd19 CD19 antigen gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:14715907 1319229 Cd19 CD19 antigen gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:12753744 1319229 Cd19 CD19 antigen gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16862162 1319229 Cd19 CD19 antigen gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21178004 1319229 Cd19 CD19 antigen gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23772037 1319229 Cd19 CD19 antigen gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15520246 1319229 Cd19 CD19 antigen gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22174151 1319229 Cd19 CD19 antigen gene MP:0002403 abnormal pre-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12818163 1319229 Cd19 CD19 antigen gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11967543 1319229 Cd19 CD19 antigen gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:12354378 1319229 Cd19 CD19 antigen gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:16148088 1319229 Cd19 CD19 antigen gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21844204 1319229 Cd19 CD19 antigen gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14563324 1319229 Cd19 CD19 antigen gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17000121 1319229 Cd19 CD19 antigen gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20150219 MGI PMID:24241423 1319229 Cd19 CD19 antigen gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11070163 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11809737 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11896394 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12563260 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16055554 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16311600 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16782029 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16862162 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17023430 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18313334 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18832734 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19270713 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23023393 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23772037 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7542548 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7543183 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20170314 MGI PMID:26301816 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20170824 MGI PMID:26443207 1319229 Cd19 CD19 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20210708 MGI PMID:32609329 1319229 Cd19 CD19 antigen gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11420047 1319229 Cd19 CD19 antigen gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11809737 1319229 Cd19 CD19 antigen gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14563324 1319229 Cd19 CD19 antigen gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15520246 1319229 Cd19 CD19 antigen gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319229 Cd19 CD19 antigen gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16862162 1319229 Cd19 CD19 antigen gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319229 Cd19 CD19 antigen gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319229 Cd19 CD19 antigen gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16055554 1319229 Cd19 CD19 antigen gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17509906 1319229 Cd19 CD19 antigen gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16148088 1319229 Cd19 CD19 antigen gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1319229 Cd19 CD19 antigen gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:7543183 1319229 Cd19 CD19 antigen gene MP:0002491 decreased IgD level IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319229 Cd19 CD19 antigen gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319229 Cd19 CD19 antigen gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:7543183 1319229 Cd19 CD19 antigen gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11070163 1319229 Cd19 CD19 antigen gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16055554 1319229 Cd19 CD19 antigen gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11070163 1319229 Cd19 CD19 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16055554 1319229 Cd19 CD19 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:17000121 1319229 Cd19 CD19 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21341261 1319229 Cd19 CD19 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1319229 Cd19 CD19 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20220616 MGI PMID:33343574 1319229 Cd19 CD19 antigen gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:16055554 1319229 Cd19 CD19 antigen gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:21341261 1319229 Cd19 CD19 antigen gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1319229 Cd19 CD19 antigen gene MP:0002495 increased IgA level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:20826752 1319229 Cd19 CD19 antigen gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15908920 1319229 Cd19 CD19 antigen gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20231207 MGI PMID:32619424 1319229 Cd19 CD19 antigen gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319229 Cd19 CD19 antigen gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:23619366 1319229 Cd19 CD19 antigen gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1319229 Cd19 CD19 antigen gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1319229 Cd19 CD19 antigen gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319229 Cd19 CD19 antigen gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20170314 MGI PMID:26301816 1319229 Cd19 CD19 antigen gene MP:0003701 elevated level of mitotic sister chromatid exchange IAGP N RGD:5509061 20170824 MGI PMID:26443207 1319229 Cd19 CD19 antigen gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:23619366 1319229 Cd19 CD19 antigen gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:23657012 1319229 Cd19 CD19 antigen gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19620304 1319229 Cd19 CD19 antigen gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1319229 Cd19 CD19 antigen gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23619366 1319229 Cd19 CD19 antigen gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:15148335 1319229 Cd19 CD19 antigen gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:17509906 1319229 Cd19 CD19 antigen gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:21341261 1319229 Cd19 CD19 antigen gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1319229 Cd19 CD19 antigen gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0004795 decreased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0004798 decreased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11509585 1319229 Cd19 CD19 antigen gene MP:0004798 decreased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16507897 1319229 Cd19 CD19 antigen gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:18832734 1319229 Cd19 CD19 antigen gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:23772037 1319229 Cd19 CD19 antigen gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:11509585 1319229 Cd19 CD19 antigen gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:11809737 1319229 Cd19 CD19 antigen gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:22547703 1319229 Cd19 CD19 antigen gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20210708 MGI PMID:32609329 1319229 Cd19 CD19 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:11420047 1319229 Cd19 CD19 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:17000121 1319229 Cd19 CD19 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:18178811 1319229 Cd19 CD19 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:19270713 1319229 Cd19 CD19 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22547703 1319229 Cd19 CD19 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:23023393 1319229 Cd19 CD19 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:23254285 1319229 Cd19 CD19 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20210708 MGI PMID:32609329 1319229 Cd19 CD19 antigen gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15908920 1319229 Cd19 CD19 antigen gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20170824 MGI PMID:26443207 1319229 Cd19 CD19 antigen gene MP:0004940 abnormal B-1 B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11070163 1319229 Cd19 CD19 antigen gene MP:0004944 abnormal B cell negative selection IAGP N RGD:5509061 20141003 MGI PMID:19896393 1319229 Cd19 CD19 antigen gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21844204 1319229 Cd19 CD19 antigen gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20200402 MGI PMID:31921164 1319229 Cd19 CD19 antigen gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21844204 1319229 Cd19 CD19 antigen gene MP:0004976 abnormal B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:11070163 1319229 Cd19 CD19 antigen gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563260 1319229 Cd19 CD19 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:11509585 1319229 Cd19 CD19 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235208 1319229 Cd19 CD19 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563260 1319229 Cd19 CD19 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12707341 1319229 Cd19 CD19 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:14564011 1319229 Cd19 CD19 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:15520246 1319229 Cd19 CD19 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16148088 1319229 Cd19 CD19 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319229 Cd19 CD19 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:17591768 1319229 Cd19 CD19 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 1319229 Cd19 CD19 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22431510 1319229 Cd19 CD19 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:7542548 1319229 Cd19 CD19 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:7543183 1319229 Cd19 CD19 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21844204 1319229 Cd19 CD19 antigen gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17509906 1319229 Cd19 CD19 antigen gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 1319229 Cd19 CD19 antigen gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563260 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16782029 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19620304 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20060366 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21178004 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21300983 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21844204 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22174151 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23619366 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20150219 MGI PMID:24241423 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20170921 MGI PMID:26668357 1319229 Cd19 CD19 antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1319229 Cd19 CD19 antigen gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11509585 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11809737 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12707341 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:14564011 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:14668867 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:14715907 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15314171 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16148088 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16166635 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16862162 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16940357 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17591768 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18538592 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19896393 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:7542548 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170314 MGI PMID:26301816 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170824 MGI PMID:26443207 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200402 MGI PMID:31921164 1319229 Cd19 CD19 antigen gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:15148335 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11163229 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11509585 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11809737 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12707341 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14715907 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16148088 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16862162 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19270713 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22547703 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7542548 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20161013 MGI PMID:23343763 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20171026 MGI PMID:22802351 1319229 Cd19 CD19 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20200402 MGI PMID:31921164 1319229 Cd19 CD19 antigen gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:20439541 1319229 Cd19 CD19 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12235208 1319229 Cd19 CD19 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12563260 1319229 Cd19 CD19 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19896393 1319229 Cd19 CD19 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21341261 1319229 Cd19 CD19 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319229 Cd19 CD19 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20170921 MGI PMID:26668357 1319229 Cd19 CD19 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20220616 MGI PMID:33343574 1319229 Cd19 CD19 antigen gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:11120817 1319229 Cd19 CD19 antigen gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20439541 1319229 Cd19 CD19 antigen gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0005432 abnormal pro-B cell morphology IAGP N RGD:5509061 20170314 MGI PMID:26301816 1319229 Cd19 CD19 antigen gene MP:0005433 absent early pro-B cells IAGP N RGD:5509061 20141003 MGI PMID:14668867 1319229 Cd19 CD19 antigen gene MP:0005434 absent late pro-B cells IAGP N RGD:5509061 20141003 MGI PMID:14668867 1319229 Cd19 CD19 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1319229 Cd19 CD19 antigen gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1319229 Cd19 CD19 antigen gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20210708 MGI PMID:32609329 1319229 Cd19 CD19 antigen gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16148088 1319229 Cd19 CD19 antigen gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19620304 1319229 Cd19 CD19 antigen gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20150219 MGI PMID:24241423 1319229 Cd19 CD19 antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16507897 1319229 Cd19 CD19 antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20150219 MGI PMID:24241423 1319229 Cd19 CD19 antigen gene MP:0008093 abnormal memory B cell number IAGP N RGD:5509061 20141003 MGI PMID:14563324 1319229 Cd19 CD19 antigen gene MP:0008093 abnormal memory B cell number IAGP N RGD:5509061 20141003 MGI PMID:14715907 1319229 Cd19 CD19 antigen gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:19620304 1319229 Cd19 CD19 antigen gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20170921 MGI PMID:26668357 1319229 Cd19 CD19 antigen gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20220616 MGI PMID:33343574 1319229 Cd19 CD19 antigen gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:14563324 1319229 Cd19 CD19 antigen gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:15189736 1319229 Cd19 CD19 antigen gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:15520246 1319229 Cd19 CD19 antigen gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319229 Cd19 CD19 antigen gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319229 Cd19 CD19 antigen gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20210826 MGI PMID:33336366 1319229 Cd19 CD19 antigen gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14563324 1319229 Cd19 CD19 antigen gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19270713 1319229 Cd19 CD19 antigen gene MP:0008100 absent plasma cells IAGP N RGD:5509061 20141003 MGI PMID:11070163 1319229 Cd19 CD19 antigen gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18313334 1319229 Cd19 CD19 antigen gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12354378 1319229 Cd19 CD19 antigen gene MP:0008136 enlarged Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:11070163 1319229 Cd19 CD19 antigen gene MP:0008164 abnormal B-1a B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0008166 abnormal B-2 B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:20060366 1319229 Cd19 CD19 antigen gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1319229 Cd19 CD19 antigen gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319229 Cd19 CD19 antigen gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0008170 decreased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1319229 Cd19 CD19 antigen gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17591768 1319229 Cd19 CD19 antigen gene MP:0008172 abnormal follicular B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0008172 abnormal follicular B cell morphology IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:11967543 1319229 Cd19 CD19 antigen gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1319229 Cd19 CD19 antigen gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:17457934 1319229 Cd19 CD19 antigen gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18313334 1319229 Cd19 CD19 antigen gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:20156974 1319229 Cd19 CD19 antigen gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21178004 1319229 Cd19 CD19 antigen gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21300983 1319229 Cd19 CD19 antigen gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1319229 Cd19 CD19 antigen gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319229 Cd19 CD19 antigen gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:11809737 1319229 Cd19 CD19 antigen gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235208 1319229 Cd19 CD19 antigen gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:14564011 1319229 Cd19 CD19 antigen gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:17457934 1319229 Cd19 CD19 antigen gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:20870947 1319229 Cd19 CD19 antigen gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21178004 1319229 Cd19 CD19 antigen gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319229 Cd19 CD19 antigen gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1319229 Cd19 CD19 antigen gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:23619366 1319229 Cd19 CD19 antigen gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319229 Cd19 CD19 antigen gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20220616 MGI PMID:33343574 1319229 Cd19 CD19 antigen gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:14715907 1319229 Cd19 CD19 antigen gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:19270713 1319229 Cd19 CD19 antigen gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21300983 1319229 Cd19 CD19 antigen gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20210708 MGI PMID:32609329 1319229 Cd19 CD19 antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563260 1319229 Cd19 CD19 antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17457934 1319229 Cd19 CD19 antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18178811 1319229 Cd19 CD19 antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18313334 1319229 Cd19 CD19 antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 1319229 Cd19 CD19 antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21178004 1319229 Cd19 CD19 antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21300983 1319229 Cd19 CD19 antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:11967543 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235208 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12354378 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12707341 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12753744 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:14564011 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16148088 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16862162 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17023430 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17457934 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17600736 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:20870947 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:22431510 1319229 Cd19 CD19 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:12753744 1319229 Cd19 CD19 antigen gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:17591768 1319229 Cd19 CD19 antigen gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:20156974 1319229 Cd19 CD19 antigen gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1319229 Cd19 CD19 antigen gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319229 Cd19 CD19 antigen gene MP:0008188 abnormal transitional stage B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1319229 Cd19 CD19 antigen gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:21178004 1319229 Cd19 CD19 antigen gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:12753744 1319229 Cd19 CD19 antigen gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:14564011 1319229 Cd19 CD19 antigen gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18538592 1319229 Cd19 CD19 antigen gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14715907 1319229 Cd19 CD19 antigen gene MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0008201 absent follicular dendritic cells IAGP N RGD:5509061 20141003 MGI PMID:12354378 1319229 Cd19 CD19 antigen gene MP:0008206 increased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1319229 Cd19 CD19 antigen gene MP:0008206 increased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21178004 1319229 Cd19 CD19 antigen gene MP:0008206 increased B-2 B cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:15520246 1319229 Cd19 CD19 antigen gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18538592 1319229 Cd19 CD19 antigen gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11420047 1319229 Cd19 CD19 antigen gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11809737 1319229 Cd19 CD19 antigen gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12818163 1319229 Cd19 CD19 antigen gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18538592 1319229 Cd19 CD19 antigen gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20200402 MGI PMID:31921164 1319229 Cd19 CD19 antigen gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 1319229 Cd19 CD19 antigen gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:23023393 1319229 Cd19 CD19 antigen gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11420047 1319229 Cd19 CD19 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11509585 1319229 Cd19 CD19 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235208 1319229 Cd19 CD19 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15520246 1319229 Cd19 CD19 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18538592 1319229 Cd19 CD19 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 1319229 Cd19 CD19 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:20870947 1319229 Cd19 CD19 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1319229 Cd19 CD19 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319229 Cd19 CD19 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319229 Cd19 CD19 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319229 Cd19 CD19 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20210708 MGI PMID:32609329 1319229 Cd19 CD19 antigen gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:12818163 1319229 Cd19 CD19 antigen gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:15908920 1319229 Cd19 CD19 antigen gene MP:0008213 absent immature B cells IAGP N RGD:5509061 20141003 MGI PMID:12818163 1319229 Cd19 CD19 antigen gene MP:0008213 absent immature B cells IAGP N RGD:5509061 20141003 MGI PMID:15908920 1319229 Cd19 CD19 antigen gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319229 Cd19 CD19 antigen gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11420047 1319229 Cd19 CD19 antigen gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235208 1319229 Cd19 CD19 antigen gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18538592 1319229 Cd19 CD19 antigen gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20170314 MGI PMID:26301816 1319229 Cd19 CD19 antigen gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:12707341 1319229 Cd19 CD19 antigen gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:19270713 1319229 Cd19 CD19 antigen gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20170921 MGI PMID:26668357 1319229 Cd19 CD19 antigen gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0008233 abnormal pro-B cell differentiation IAGP N RGD:5509061 20170314 MGI PMID:26301816 1319229 Cd19 CD19 antigen gene MP:0008240 abnormal spleen marginal zone macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19620304 1319229 Cd19 CD19 antigen gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12354378 1319229 Cd19 CD19 antigen gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18663224 1319229 Cd19 CD19 antigen gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20870947 1319229 Cd19 CD19 antigen gene MP:0008473 abnormal spleen follicular dendritic cell network IAGP N RGD:5509061 20141003 MGI PMID:12354378 1319229 Cd19 CD19 antigen gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:12563260 1319229 Cd19 CD19 antigen gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:7543183 1319229 Cd19 CD19 antigen gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:20060366 1319229 Cd19 CD19 antigen gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:14563324 1319229 Cd19 CD19 antigen gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319229 Cd19 CD19 antigen gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:12354378 1319229 Cd19 CD19 antigen gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:12563260 1319229 Cd19 CD19 antigen gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:14563324 1319229 Cd19 CD19 antigen gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319229 Cd19 CD19 antigen gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:12354378 1319229 Cd19 CD19 antigen gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:21300983 1319229 Cd19 CD19 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11420047 1319229 Cd19 CD19 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11509585 1319229 Cd19 CD19 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319229 Cd19 CD19 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16455962 1319229 Cd19 CD19 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:7542548 1319229 Cd19 CD19 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:7543183 1319229 Cd19 CD19 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160721 MGI PMID:26366712 1319229 Cd19 CD19 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319229 Cd19 CD19 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20231102 MGI PMID:35439434 1319229 Cd19 CD19 antigen gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16455962 1319229 Cd19 CD19 antigen gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:7542548 1319229 Cd19 CD19 antigen gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:11509585 1319229 Cd19 CD19 antigen gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:7542548 1319229 Cd19 CD19 antigen gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11420047 1319229 Cd19 CD19 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319229 Cd19 CD19 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:16455962 1319229 Cd19 CD19 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:19270713 1319229 Cd19 CD19 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:7542548 1319229 Cd19 CD19 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:21341261 1319229 Cd19 CD19 antigen gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11967543 1319229 Cd19 CD19 antigen gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:16166635 1319229 Cd19 CD19 antigen gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:11120817 1319229 Cd19 CD19 antigen gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16507897 1319229 Cd19 CD19 antigen gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:19620304 1319229 Cd19 CD19 antigen gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1319229 Cd19 CD19 antigen gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319229 Cd19 CD19 antigen gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:16507897 1319229 Cd19 CD19 antigen gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0008728 increased memory B cell number IAGP N RGD:5509061 20210826 MGI PMID:33336366 1319229 Cd19 CD19 antigen gene MP:0008746 abnormal peripheral B cell anergy IAGP N RGD:5509061 20141003 MGI PMID:19896393 1319229 Cd19 CD19 antigen gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12563260 1319229 Cd19 CD19 antigen gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12707341 1319229 Cd19 CD19 antigen gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14668867 1319229 Cd19 CD19 antigen gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16862162 1319229 Cd19 CD19 antigen gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319229 Cd19 CD19 antigen gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20210708 MGI PMID:32609329 1319229 Cd19 CD19 antigen gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16782029 1319229 Cd19 CD19 antigen gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20705491 1319229 Cd19 CD19 antigen gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21300983 1319229 Cd19 CD19 antigen gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:15908920 1319229 Cd19 CD19 antigen gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16782029 1319229 Cd19 CD19 antigen gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20220616 MGI PMID:33343574 1319229 Cd19 CD19 antigen gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:15908920 1319229 Cd19 CD19 antigen gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17723217 1319229 Cd19 CD19 antigen gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0009317 increased follicular lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0009318 increased splenic marginal zone lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0009319 increased small lymphocytic lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22174151 1319229 Cd19 CD19 antigen gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1319229 Cd19 CD19 antigen gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319229 Cd19 CD19 antigen gene MP:0009623 enlarged inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11120817 1319229 Cd19 CD19 antigen gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11967543 1319229 Cd19 CD19 antigen gene MP:0009921 abnormal transitional stage T3 B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0009922 increased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:20156974 1319229 Cd19 CD19 antigen gene MP:0009922 increased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:24242374 1319229 Cd19 CD19 antigen gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319229 Cd19 CD19 antigen gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:20156974 1319229 Cd19 CD19 antigen gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319229 Cd19 CD19 antigen gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18467694 1319229 Cd19 CD19 antigen gene MP:0010138 arteritis IAGP N RGD:5509061 20141003 MGI PMID:17513743 1319229 Cd19 CD19 antigen gene MP:0010228 decreased transitional stage T3 B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319229 Cd19 CD19 antigen gene MP:0010274 increased organ/body region tumor incidence IAGP N RGD:5509061 20231207 MGI PMID:32619424 1319229 Cd19 CD19 antigen gene MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22341446 1319229 Cd19 CD19 antigen gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21930766 1319229 Cd19 CD19 antigen gene MP:0010337 increased chronic lymphocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:22174151 1319229 Cd19 CD19 antigen gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170921 MGI PMID:26668357 1319229 Cd19 CD19 antigen gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:23619366 1319229 Cd19 CD19 antigen gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20956547 1319229 Cd19 CD19 antigen gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22174151 1319229 Cd19 CD19 antigen gene MP:0013940 abnormal plasmablast number IAGP N RGD:5509061 20170921 MGI PMID:26668357 1319229 Cd19 CD19 antigen gene MP:0013940 abnormal plasmablast number IAGP N RGD:5509061 20210506 MGI PMID:32547538 1319229 Cd19 CD19 antigen gene MP:0013940 abnormal plasmablast number IAGP N RGD:5509061 20210826 MGI PMID:33336366 1319229 Cd19 CD19 antigen gene MP:0014050 increased B cell acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20170314 MGI PMID:26301816 1319229 Cd19 CD19 antigen gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:21339646 1319229 Cd19 CD19 antigen gene MP:0014347 increased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:18490492 1319229 Cd19 CD19 antigen gene MP:0014348 decreased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:21795747 1319229 Cd19 CD19 antigen gene MP:0020154 impaired humoral immune response IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319229 Cd19 CD19 antigen gene MP:0020154 impaired humoral immune response IAGP N RGD:5509061 20210826 MGI PMID:33336366 1319229 Cd19 CD19 antigen gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:17513743 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20230601 MGI 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230601 MGI 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230406 MGI PMID:32209662 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230601 MGI 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230601 MGI 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20230601 MGI 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20230601 MGI 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20230406 MGI PMID:32209662 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20230601 MGI 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20230601 MGI 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0010096 abnormal incisor color IEA N RGD:5509061 20230601 MGI 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0012216 decreased plasmalogen level IAGP N RGD:5509061 20230406 MGI PMID:32209662 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0012216 decreased plasmalogen level IAGP N RGD:5509061 20240808 MGI PMID:36690320 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0012218 decreased brain plasmalogen level IAGP N RGD:5509061 20230406 MGI PMID:32209662 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0012218 decreased brain plasmalogen level IAGP N RGD:5509061 20240808 MGI PMID:36690320 1319239 Peds1 plasmanylethanolamine desaturase 1 gene MP:0012220 abnormal ether lipid level IAGP N RGD:5509061 20240808 MGI PMID:36690320 1319243 Bcl9l B cell CLL/lymphoma 9-like gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:19699733 1319243 Bcl9l B cell CLL/lymphoma 9-like gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1319243 Bcl9l B cell CLL/lymphoma 9-like gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20211104 MGI PMID:22109522 1319243 Bcl9l B cell CLL/lymphoma 9-like gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20211104 MGI PMID:22109522 1319243 Bcl9l B cell CLL/lymphoma 9-like gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20211104 MGI PMID:22109522 1319243 Bcl9l B cell CLL/lymphoma 9-like gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20211104 MGI PMID:22109522 1319243 Bcl9l B cell CLL/lymphoma 9-like gene MP:0004266 pale placenta IAGP N RGD:5509061 20211104 MGI PMID:22109522 1319243 Bcl9l B cell CLL/lymphoma 9-like gene MP:0004560 abnormal chorionic plate morphology IAGP N RGD:5509061 20211104 MGI PMID:22109522 1319243 Bcl9l B cell CLL/lymphoma 9-like gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20211104 MGI PMID:22109522 1319243 Bcl9l B cell CLL/lymphoma 9-like gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:19699733 1319243 Bcl9l B cell CLL/lymphoma 9-like gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20211104 MGI PMID:22109522 1319243 Bcl9l B cell CLL/lymphoma 9-like gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1319243 Bcl9l B cell CLL/lymphoma 9-like gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:19699733 1319247 Ptk6 PTK6 protein tyrosine kinase 6 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:16782882 1319247 Ptk6 PTK6 protein tyrosine kinase 6 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20181227 MGI 1319247 Ptk6 PTK6 protein tyrosine kinase 6 gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:16782882 1319247 Ptk6 PTK6 protein tyrosine kinase 6 gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20141003 MGI PMID:16782882 1319249 Dnal4 dynein, axonemal, light chain 4 gene MP:0000745 tremors IEA N RGD:5509061 20210826 MGI 1319249 Dnal4 dynein, axonemal, light chain 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1319249 Dnal4 dynein, axonemal, light chain 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20190718 MGI PMID:30442762 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20201231 MGI 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20190718 MGI PMID:30442762 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201231 MGI 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190718 MGI PMID:30442762 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20190718 MGI PMID:30442762 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0002083 premature death IAGP N RGD:5509061 20190718 MGI PMID:30442762 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20190718 MGI PMID:30442762 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0004472 broad nasal bone IAGP N RGD:5509061 20190718 MGI PMID:30442762 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20190718 MGI PMID:30442762 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20190718 MGI PMID:30442762 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20190718 MGI PMID:30442762 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20200402 MGI 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0010832 lethality during fetal growth through weaning IAGP N RGD:5509061 20190718 MGI PMID:30442762 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20190718 MGI PMID:30442762 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20190718 MGI PMID:30442762 1319251 Lztr1 leucine-zipper-like transcriptional regulator, 1 gene MP:0030280 short parietal bone IAGP N RGD:5509061 20190718 MGI PMID:30442762 1319253 Cep68 centrosomal protein 68 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1319253 Cep68 centrosomal protein 68 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1319253 Cep68 centrosomal protein 68 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220519 MGI 1319255 Trappc8 trafficking protein particle complex 8 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20240523 MGI 1319255 Trappc8 trafficking protein particle complex 8 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20240523 MGI 1319255 Trappc8 trafficking protein particle complex 8 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1319255 Trappc8 trafficking protein particle complex 8 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1319255 Trappc8 trafficking protein particle complex 8 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20240523 MGI 1319255 Trappc8 trafficking protein particle complex 8 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1319255 Trappc8 trafficking protein particle complex 8 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0000914 exencephaly IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0000929 open neural tube IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0004264 abnormal extraembryonic tissue physiology IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0012681 collapsed brain ventricles IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0012706 decreased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0013227 small brain ventricles IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0014260 embryonic lethality prior to organogenesis, incomplete penetrance IAGP N RGD:5509061 20230706 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0020252 abnormal collagen level IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20170202 MGI PMID:26494538 1319256 Sec23a SEC23 homolog A, COPII coat complex component gene MP:0020413 increased amnion apoptosis IAGP N RGD:5509061 20170223 MGI PMID:26494538 1319258 1700025G04Rik RIKEN cDNA 1700025G04 gene gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1319258 1700025G04Rik RIKEN cDNA 1700025G04 gene gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1319258 1700025G04Rik RIKEN cDNA 1700025G04 gene gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1319258 1700025G04Rik RIKEN cDNA 1700025G04 gene gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1319258 1700025G04Rik RIKEN cDNA 1700025G04 gene gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20210128 MGI 1319258 1700025G04Rik RIKEN cDNA 1700025G04 gene gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1319258 1700025G04Rik RIKEN cDNA 1700025G04 gene gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1319258 1700025G04Rik RIKEN cDNA 1700025G04 gene gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1319258 1700025G04Rik RIKEN cDNA 1700025G04 gene gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1319258 1700025G04Rik RIKEN cDNA 1700025G04 gene gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1319260 Cox20 cytochrome c oxidase assembly protein 20 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20181227 MGI 1319260 Cox20 cytochrome c oxidase assembly protein 20 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20181227 MGI 1319260 Cox20 cytochrome c oxidase assembly protein 20 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230601 MGI 1319260 Cox20 cytochrome c oxidase assembly protein 20 gene MP:0002989 small kidney IEA N RGD:5509061 20240523 MGI 1319260 Cox20 cytochrome c oxidase assembly protein 20 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1319260 Cox20 cytochrome c oxidase assembly protein 20 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1319260 Cox20 cytochrome c oxidase assembly protein 20 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000381 enlarged hair follicles IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001202 skin photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150924 MGI PMID:25951169 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20150924 MGI PMID:25951169 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20150924 MGI PMID:25951169 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001306 small lens IAGP N RGD:5509061 20150924 MGI PMID:25951169 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001588 abnormal hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19114557 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20150924 MGI PMID:25951169 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:19114557 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0002879 increased cellular sensitivity to X-ray irradiation IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22174697 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0003848 brittle hair IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0003848 brittle hair IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0003849 greasy coat IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0003849 greasy coat IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:19114557 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:19114557 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:22174697 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0010179 rough coat IAGP N RGD:5509061 20150924 MGI PMID:25951169 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0010202 focal dorsal hair loss IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20150924 MGI PMID:25951169 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9651581 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0010699 dilated hair follicle IAGP N RGD:5509061 20181129 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16904611 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19114557 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11950998 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17020410 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9426063 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20150924 MGI PMID:25951169 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0012734 abnormal response to radiation IAGP N RGD:5509061 20150924 MGI PMID:25951169 1319265 Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 gene MP:0031345 developmental cataract IAGP N RGD:5509061 20220217 MGI PMID:25951169 1319268 Rab24 RAB24, member RAS oncogene family gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1319268 Rab24 RAB24, member RAS oncogene family gene MP:0001307 fused cornea and lens IEA N RGD:5509061 20240523 MGI 1319268 Rab24 RAB24, member RAS oncogene family gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20170105 MGI 1319268 Rab24 RAB24, member RAS oncogene family gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1319268 Rab24 RAB24, member RAS oncogene family gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160421 MGI 1319268 Rab24 RAB24, member RAS oncogene family gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1319270 Hoxb13 homeobox B13 gene MP:0000588 thick tail IAGP N RGD:5509061 20141003 MGI PMID:12679105 1319270 Hoxb13 homeobox B13 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:12679105 1319270 Hoxb13 homeobox B13 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:12679105 1319270 Hoxb13 homeobox B13 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12679105 1319270 Hoxb13 homeobox B13 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:12679105 1319270 Hoxb13 homeobox B13 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12679105 1319270 Hoxb13 homeobox B13 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:12679105 1319270 Hoxb13 homeobox B13 gene MP:0002758 long tail IAGP N RGD:5509061 20141003 MGI PMID:12679105 1319270 Hoxb13 homeobox B13 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12679105 1319270 Hoxb13 homeobox B13 gene MP:0002809 increased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:12679105 1319270 Hoxb13 homeobox B13 gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:12668621 1319270 Hoxb13 homeobox B13 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:12679105 1319270 Hoxb13 homeobox B13 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:12679105 1319270 Hoxb13 homeobox B13 gene MP:0009380 abnormal prostate gland ventral lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:12668621 1319270 Hoxb13 homeobox B13 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:12679105 1319270 Hoxb13 homeobox B13 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10485650 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11239451 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12387736 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12468431 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8934575 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9639496 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8934575 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210805 MGI 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0000274 enlarged heart IEA N RGD:5509061 20210805 MGI 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:12387736 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:9639496 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:8934575 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:10485650 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22042698 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22042698 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20210805 MGI 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210805 MGI 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0001147 small testis IEA N RGD:5509061 20210805 MGI 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:9989983 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:8934575 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:9639496 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0002415 abnormal neutrophil differentiation IAGP N RGD:5509061 20141003 MGI PMID:9639496 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:12387736 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0002620 abnormal monocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8934575 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:8934575 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10485650 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11239451 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:22042698 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10485650 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12387736 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0009709 hydrometra IEA N RGD:5509061 20210805 MGI 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22042698 1319272 Csf3r colony stimulating factor 3 receptor gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210805 MGI 1319280 Fkbp10 FK506 binding protein 10 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20151210 MGI PMID:24777781 1319280 Fkbp10 FK506 binding protein 10 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20151210 MGI PMID:24777781 1319280 Fkbp10 FK506 binding protein 10 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20151210 MGI PMID:24777781 1319280 Fkbp10 FK506 binding protein 10 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20151210 MGI PMID:24777781 1319280 Fkbp10 FK506 binding protein 10 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1319280 Fkbp10 FK506 binding protein 10 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20160804 MGI 1319280 Fkbp10 FK506 binding protein 10 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160804 MGI 1319280 Fkbp10 FK506 binding protein 10 gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20160804 MGI 1319280 Fkbp10 FK506 binding protein 10 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20160804 MGI 1319280 Fkbp10 FK506 binding protein 10 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20151210 MGI PMID:24777781 1319280 Fkbp10 FK506 binding protein 10 gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20151210 MGI PMID:24777781 1319280 Fkbp10 FK506 binding protein 10 gene MP:0010997 decreased aorta wall thickness IAGP N RGD:5509061 20151210 MGI PMID:24777781 1319280 Fkbp10 FK506 binding protein 10 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20151210 MGI PMID:24777781 1319280 Fkbp10 FK506 binding protein 10 gene MP:0011642 abnormal bone collagen fibril morphology IAGP N RGD:5509061 20151210 MGI PMID:24777781 1319280 Fkbp10 FK506 binding protein 10 gene MP:0013258 abnormal extracellular matrix morphology IAGP N RGD:5509061 20151210 MGI PMID:24777781 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20210325 MGI PMID:33220177 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20210325 MGI PMID:33220177 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20210325 MGI PMID:33220177 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20210325 MGI PMID:33220177 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20210325 MGI PMID:33220177 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20210325 MGI PMID:33220177 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20201022 MGI 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20210325 MGI PMID:33220177 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20221215 MGI 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20210325 MGI PMID:33220177 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20210325 MGI PMID:33220177 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20210325 MGI PMID:33220177 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0012559 decreased forebrain volume IAGP N RGD:5509061 20210325 MGI PMID:33220177 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1319282 Ppil1 peptidylprolyl isomerase (cyclophilin)-like 1 gene MP:0020602 decreased cerebral cortex average cell area IAGP N RGD:5509061 20210325 MGI PMID:33220177 1319286 Hspb9 heat shock protein, alpha-crystallin-related, B9 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1319286 Hspb9 heat shock protein, alpha-crystallin-related, B9 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1319286 Hspb9 heat shock protein, alpha-crystallin-related, B9 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210826 MGI 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:20442420 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20442420 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0001391 abnormal tail movements IEA N RGD:5509061 20141003 MGI 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:20442420 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0001867 rhinitis IAGP N RGD:5509061 20141003 MGI PMID:20442420 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20442420 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0001947 abnormal mucociliary clearance IAGP N RGD:5509061 20141003 MGI PMID:20498047 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0001950 abnormal respiratory sounds IAGP N RGD:5509061 20141003 MGI PMID:20498047 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20498047 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20442420 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:20442420 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20442420 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:20442420 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:20442420 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20141003 MGI PMID:20442420 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:20498047 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:20442420 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:20498047 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:20498047 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220714 MGI PMID:20442420 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0030118 rhinosinusitis IAGP N RGD:5509061 20210211 MGI PMID:20498047 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0031088 coughing IAGP N RGD:5509061 20210211 MGI PMID:20498047 1319290 Ttll1 tubulin tyrosine ligase-like 1 gene MP:0031089 sneezing IAGP N RGD:5509061 20210211 MGI PMID:20498047 1319295 Fbxl16 F-box and leucine-rich repeat protein 16 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1319295 Fbxl16 F-box and leucine-rich repeat protein 16 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1319299 Ndufb8 NADH:ubiquinone oxidoreductase subunit B8 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319299 Ndufb8 NADH:ubiquinone oxidoreductase subunit B8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319299 Ndufb8 NADH:ubiquinone oxidoreductase subunit B8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:19139267 1319301 Cert1 ceramide transporter 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19139267 1319301 Cert1 ceramide transporter 1 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19139267 1319301 Cert1 ceramide transporter 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:21832087 1319301 Cert1 ceramide transporter 1 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:19139267 1319301 Cert1 ceramide transporter 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19139267 1319301 Cert1 ceramide transporter 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319301 Cert1 ceramide transporter 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19139267 1319301 Cert1 ceramide transporter 1 gene MP:0002237 abnormal nasal cavity morphology IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0002428 abnormal semicircular canal morphology IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0002728 absent tibia IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0003078 aphakia IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0004201 fetal growth retardation IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0004259 small placenta IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319301 Cert1 ceramide transporter 1 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0004612 fusion of vertebral bodies IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0004646 decreased cervical vertebrae number IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319301 Cert1 ceramide transporter 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19139267 1319301 Cert1 ceramide transporter 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19139267 1319301 Cert1 ceramide transporter 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20240711 MGI PMID:19139267 1319301 Cert1 ceramide transporter 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:19139267 1319301 Cert1 ceramide transporter 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:19139267 1319301 Cert1 ceramide transporter 1 gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20141003 MGI PMID:19139267 1319301 Cert1 ceramide transporter 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319301 Cert1 ceramide transporter 1 gene MP:0008922 abnormal cervical rib IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:19139267 1319301 Cert1 ceramide transporter 1 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0010496 abnormal pectinate muscle morphology IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0010572 persistent right dorsal aorta IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19139267 1319301 Cert1 ceramide transporter 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319301 Cert1 ceramide transporter 1 gene MP:0013247 placenta necrosis IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319301 Cert1 ceramide transporter 1 gene MP:0013985 abnormal umbilical vein topology IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0020500 persistent trigeminal artery IEA N RGD:5509061 20180628 MGI 1319301 Cert1 ceramide transporter 1 gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:29539633 1319301 Cert1 ceramide transporter 1 gene MP:0031594 increased cardiac jelly amount IAGP N RGD:5509061 20240229 MGI PMID:19139267 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20230601 MGI PMID:30135927 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0002891 increased insulin sensitivity IEA N RGD:5509061 20170817 MGI 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0004889 increased energy expenditure IEA N RGD:5509061 20170817 MGI 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20170817 MGI PMID:21552327 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0005439 decreased glycogen level IAGP N RGD:5509061 20141003 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191128 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20191128 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0014063 Lafora bodies IAGP N RGD:5509061 20230601 MGI PMID:30135927 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0014072 decreased cardiac muscle glycogen level IAGP N RGD:5509061 20191128 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0030021 increased muscle cell glucose uptake IEA N RGD:5509061 20170817 MGI 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0030994 decreased adipose tissue glycogen level IAGP N RGD:5509061 20191128 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:12727934 1319303 Ppp1r3c protein phosphatase 1, regulatory subunit 3C gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:12727934 1319305 Pkp3 plakophilin 3 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0000405 abnormal auchene hair morphology IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0000424 retarded hair growth IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0003812 abnormal hair medulla IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0003846 matted coat IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0003848 brittle hair IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0008768 abnormal hair medulla air spaces IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:18079750 1319305 Pkp3 plakophilin 3 gene MP:0011195 increased hair follicle apoptosis IAGP N RGD:5509061 20181129 MGI PMID:18079750 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:15539463 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15173597 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15322545 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15173597 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:15322545 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:15173597 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:15539463 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15173597 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:15322545 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:15539463 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15539463 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20210211 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20210211 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0003537 hydrometrocolpos IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16170314 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20191128 MGI PMID:31479441 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0005195 abnormal posterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20210211 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:15539463 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0005633 increased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:15539463 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18032602 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15322545 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:18032602 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0006357 abnormal circulating mineral level IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:18032602 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:18032602 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:18032602 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:15173597 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20191128 MGI PMID:31479441 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20191128 MGI PMID:31479441 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15173597 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15322545 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15173597 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:15539463 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20210211 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0010092 increased circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:17519557 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15322545 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15173597 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0011281 abnormal olfactory epithelium cilium morphology IAGP N RGD:5509061 20160407 MGI PMID:15322545 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210211 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20170202 MGI PMID:16794820 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20191128 MGI PMID:31479441 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0020511 decreased dendritic spine length IAGP N RGD:5509061 20191128 MGI PMID:31479441 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20191128 MGI PMID:31479441 1319307 Bbs4 Bardet-Biedl syndrome 4 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:15173597 1319310 Nrn1l neuritin 1-like gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1319310 Nrn1l neuritin 1-like gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 1319310 Nrn1l neuritin 1-like gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0000921 demyelination IAGP N RGD:5509061 20201210 MGI PMID:31199454 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0000921 demyelination IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:31199454 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:31199454 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:31199454 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0001407 short stride length IAGP N RGD:5509061 20200310 MGI PMID:31199454 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0001407 short stride length IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:31199454 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0001513 limb grasping IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20201210 MGI PMID:31199454 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20201210 MGI PMID:31199454 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0004262 abnormal physical strength IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38697008 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200310 MGI PMID:31199454 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20201210 MGI PMID:31199454 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20201210 MGI PMID:31199454 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0009434 paraparesis IAGP N RGD:5509061 20200310 MGI PMID:31199454 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:31199454 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0010738 abnormal internode morphology IAGP N RGD:5509061 20201210 MGI PMID:31199454 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0010738 abnormal internode morphology IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0011730 increased myelin sheath thickness IAGP N RGD:5509061 20201210 MGI PMID:31199454 1319313 Cfap276 cilia and flagella associated protein 276 gene MP:0011730 increased myelin sheath thickness IAGP N RGD:5509061 20201210 MGI PMID:32592472 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20221215 MGI 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:21765887 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15247420 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21765887 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21765887 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14983020 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:14983020 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21765887 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15247420 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15247420 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23722907 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:14983020 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:21765887 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19381288 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15247420 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:14983020 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:14983020 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20230601 MGI 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21765887 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21765887 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20141003 MGI PMID:14983020 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23722907 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:14983020 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15247420 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20230601 MGI 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14983020 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14983020 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15247420 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21765887 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15247420 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14983020 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21765887 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20141003 MGI PMID:14983020 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0011332 abnormal kidney outer medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:14983020 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14983020 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0011378 abnormal kidney outer medulla inner stripe morphology IAGP N RGD:5509061 20141003 MGI PMID:14983020 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:14983020 1319319 Nfat5 nuclear factor of activated T cells 5 gene MP:0012007 abnormal chloride level IAGP N RGD:5509061 20141003 MGI PMID:23722907 1319321 Dlk2 delta like non-canonical Notch ligand 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20201029 MGI PMID:28863347 1319321 Dlk2 delta like non-canonical Notch ligand 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20201029 MGI PMID:28863347 1319321 Dlk2 delta like non-canonical Notch ligand 2 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20201029 MGI PMID:28863347 1319321 Dlk2 delta like non-canonical Notch ligand 2 gene MP:0014414 increased depression-related behavior IAGP N RGD:5509061 20240425 MGI PMID:28863347 1319322 Thnsl2 threonine synthase-like 2 (bacterial) gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20231207 MGI 1319322 Thnsl2 threonine synthase-like 2 (bacterial) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1319322 Thnsl2 threonine synthase-like 2 (bacterial) gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1319322 Thnsl2 threonine synthase-like 2 (bacterial) gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1319334 Jade2 jade family PHD finger 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1319334 Jade2 jade family PHD finger 2 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210826 MGI 1319334 Jade2 jade family PHD finger 2 gene MP:0000692 small spleen IEA N RGD:5509061 20210826 MGI 1319334 Jade2 jade family PHD finger 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20240822 MGI PMID:36008159 1319334 Jade2 jade family PHD finger 2 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20240822 MGI PMID:36008159 1319334 Jade2 jade family PHD finger 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1319334 Jade2 jade family PHD finger 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20240822 MGI PMID:36008159 1319334 Jade2 jade family PHD finger 2 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20240822 MGI PMID:36008159 1319334 Jade2 jade family PHD finger 2 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20240822 MGI PMID:36008159 1319334 Jade2 jade family PHD finger 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200514 MGI 1319334 Jade2 jade family PHD finger 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1319334 Jade2 jade family PHD finger 2 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210826 MGI 1319334 Jade2 jade family PHD finger 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20200514 MGI 1319334 Jade2 jade family PHD finger 2 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240822 MGI PMID:36008159 1319334 Jade2 jade family PHD finger 2 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240822 MGI PMID:36008159 1319334 Jade2 jade family PHD finger 2 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20240822 MGI PMID:36008159 1319336 Smyd5 SET and MYND domain containing 5 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20240926 MGI PMID:35643234 1319336 Smyd5 SET and MYND domain containing 5 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1319336 Smyd5 SET and MYND domain containing 5 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20240926 MGI PMID:35643234 1319337 Cst7 cystatin F (leukocystatin) gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1319339 Fkbp5 FK506 binding protein 5 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 1319339 Fkbp5 FK506 binding protein 5 gene MP:0001314 cornea opacity IEA N RGD:5509061 20181227 MGI 1319339 Fkbp5 FK506 binding protein 5 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21935478 1319339 Fkbp5 FK506 binding protein 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17142810 1319339 Fkbp5 FK506 binding protein 5 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20231207 MGI 1319339 Fkbp5 FK506 binding protein 5 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:21935478 1319339 Fkbp5 FK506 binding protein 5 gene MP:0003124 hypospadia IAGP N RGD:5509061 20141003 MGI PMID:17142810 1319339 Fkbp5 FK506 binding protein 5 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20210128 MGI 1319339 Fkbp5 FK506 binding protein 5 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220811 MGI 1319339 Fkbp5 FK506 binding protein 5 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17142810 1319339 Fkbp5 FK506 binding protein 5 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1319339 Fkbp5 FK506 binding protein 5 gene MP:0014413 decreased depression-related behavior IAGP N RGD:5509061 20240425 MGI PMID:21935478 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16470614 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:14706070 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:11892011 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16470614 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20150625 MGI PMID:10328999 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:16470614 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:3410318 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000592 short tail IEA N RGD:5509061 20111116 MGI 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:14169723 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16245024 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000745 tremors IAGP N RGD:5509061 20150611 MGI PMID:20506478 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16245024 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:14169723 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:16245024 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:2051161 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000921 demyelination IAGP N RGD:5509061 20150611 MGI PMID:20506478 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:14706070 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:14706070 1319347 Qki quaking, KH domain containing RNA binding gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16245024 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:14757819 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:5955164 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:5955164 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16245024 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:5955164 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150611 MGI PMID:20506478 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:5955164 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001407 short stride length IAGP N RGD:5509061 20150611 MGI PMID:20506478 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:5955164 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:14706070 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11892011 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:3410318 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14706070 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:3410318 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:14706070 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:16470614 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:3410318 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:14169723 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001925 male infertility IAGP N RGD:5509061 20201022 MGI PMID:15148410 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14757819 1319347 Qki quaking, KH domain containing RNA binding gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20201022 MGI PMID:15148410 1319347 Qki quaking, KH domain containing RNA binding gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16245024 1319347 Qki quaking, KH domain containing RNA binding gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20111116 MGI 1319347 Qki quaking, KH domain containing RNA binding gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16245024 1319347 Qki quaking, KH domain containing RNA binding gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:3410318 1319347 Qki quaking, KH domain containing RNA binding gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20111116 MGI 1319347 Qki quaking, KH domain containing RNA binding gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:14706070 1319347 Qki quaking, KH domain containing RNA binding gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:14706070 1319347 Qki quaking, KH domain containing RNA binding gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:14757819 1319347 Qki quaking, KH domain containing RNA binding gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15148410 1319347 Qki quaking, KH domain containing RNA binding gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:14169723 1319347 Qki quaking, KH domain containing RNA binding gene MP:0002826 tonic seizures IAGP N RGD:5509061 20150611 MGI PMID:20506478 1319347 Qki quaking, KH domain containing RNA binding gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11892011 1319347 Qki quaking, KH domain containing RNA binding gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16470614 1319347 Qki quaking, KH domain containing RNA binding gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20180125 MGI PMID:14706070 1319347 Qki quaking, KH domain containing RNA binding gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:5955164 1319347 Qki quaking, KH domain containing RNA binding gene MP:0003492 abnormal involuntary movement IEA N RGD:5509061 20111116 MGI 1319347 Qki quaking, KH domain containing RNA binding gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:3410318 1319347 Qki quaking, KH domain containing RNA binding gene MP:0003871 abnormal myelin sheath morphology IEA N RGD:5509061 20111116 MGI 1319347 Qki quaking, KH domain containing RNA binding gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16470614 1319347 Qki quaking, KH domain containing RNA binding gene MP:0004077 abnormal striatum morphology IEA N RGD:5509061 20111116 MGI 1319347 Qki quaking, KH domain containing RNA binding gene MP:0004814 reduced linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 1319347 Qki quaking, KH domain containing RNA binding gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20150625 MGI PMID:10328999 1319347 Qki quaking, KH domain containing RNA binding gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:11892011 1319347 Qki quaking, KH domain containing RNA binding gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:14706070 1319347 Qki quaking, KH domain containing RNA binding gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16470614 1319347 Qki quaking, KH domain containing RNA binding gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14706070 1319347 Qki quaking, KH domain containing RNA binding gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:3410318 1319347 Qki quaking, KH domain containing RNA binding gene MP:0006057 decreased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:16470614 1319347 Qki quaking, KH domain containing RNA binding gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20141003 MGI PMID:16470614 1319347 Qki quaking, KH domain containing RNA binding gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:3410318 1319347 Qki quaking, KH domain containing RNA binding gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:16245024 1319347 Qki quaking, KH domain containing RNA binding gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20150625 MGI PMID:10328999 1319347 Qki quaking, KH domain containing RNA binding gene MP:0008533 abnormal anterior visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16470614 1319347 Qki quaking, KH domain containing RNA binding gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:14757819 1319347 Qki quaking, KH domain containing RNA binding gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:14757819 1319347 Qki quaking, KH domain containing RNA binding gene MP:0009325 necrospermia IAGP N RGD:5509061 20141003 MGI PMID:14757819 1319347 Qki quaking, KH domain containing RNA binding gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:14169723 1319347 Qki quaking, KH domain containing RNA binding gene MP:0010734 abnormal paranode morphology IAGP N RGD:5509061 20150611 MGI PMID:20506478 1319347 Qki quaking, KH domain containing RNA binding gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1319347 Qki quaking, KH domain containing RNA binding gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:3410318 1319347 Qki quaking, KH domain containing RNA binding gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20150625 MGI PMID:10328999 1319347 Qki quaking, KH domain containing RNA binding gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:3410318 1319347 Qki quaking, KH domain containing RNA binding gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:3410318 1319347 Qki quaking, KH domain containing RNA binding gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11892011 1319347 Qki quaking, KH domain containing RNA binding gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14706070 1319347 Qki quaking, KH domain containing RNA binding gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16470614 1319347 Qki quaking, KH domain containing RNA binding gene MP:0011257 abnormal head fold morphology IAGP N RGD:5509061 20150625 MGI PMID:10328999 1319347 Qki quaking, KH domain containing RNA binding gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20150611 MGI PMID:20506478 1319349 Gpr155 G protein-coupled receptor 155 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1319349 Gpr155 G protein-coupled receptor 155 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20210128 MGI 1319349 Gpr155 G protein-coupled receptor 155 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1319349 Gpr155 G protein-coupled receptor 155 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1319349 Gpr155 G protein-coupled receptor 155 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1319349 Gpr155 G protein-coupled receptor 155 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1319354 Cldn14 claudin 14 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:12913076 1319354 Cldn14 claudin 14 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12913076 1319354 Cldn14 claudin 14 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12913076 1319354 Cldn14 claudin 14 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12913076 1319354 Cldn14 claudin 14 gene MP:0004530 absent outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:12913076 1319354 Cldn14 claudin 14 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:12913076 1319354 Cldn14 claudin 14 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12913076 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:11894097 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15691841 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18261938 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11894098 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11894097 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11894098 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:11894098 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:11894097 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:11894098 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18261938 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11894097 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:11894098 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:18261938 1319358 Ripk2 receptor (TNFRSF)-interacting serine-threonine kinase 2 gene MP:0012564 decreased tumor incidence following infection IAGP N RGD:5509061 20241114 MGI PMID:36103821 1319360 Trim45 tripartite motif-containing 45 gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20170504 MGI 1319360 Trim45 tripartite motif-containing 45 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1319360 Trim45 tripartite motif-containing 45 gene MP:0003078 aphakia IEA N RGD:5509061 20170504 MGI 1319360 Trim45 tripartite motif-containing 45 gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20170504 MGI 1319360 Trim45 tripartite motif-containing 45 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 1319360 Trim45 tripartite motif-containing 45 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1319360 Trim45 tripartite motif-containing 45 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20170504 MGI 1319360 Trim45 tripartite motif-containing 45 gene MP:0010484 bicuspid aortic valve IEA N RGD:5509061 20170504 MGI 1319360 Trim45 tripartite motif-containing 45 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319360 Trim45 tripartite motif-containing 45 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1319360 Trim45 tripartite motif-containing 45 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1319360 Trim45 tripartite motif-containing 45 gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20170504 MGI 1319360 Trim45 tripartite motif-containing 45 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 1319360 Trim45 tripartite motif-containing 45 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1319360 Trim45 tripartite motif-containing 45 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1319360 Trim45 tripartite motif-containing 45 gene MP:0014003 additional anastomosis between intracranial vertebral arteries IEA N RGD:5509061 20170504 MGI 1319362 4930579F01Rik RIKEN cDNA 4930579F01 gene gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1319362 4930579F01Rik RIKEN cDNA 4930579F01 gene gene MP:0005655 increased aggression IEA N RGD:5509061 20240523 MGI 1319363 Kif18a kinesin family member 18A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20981276 1319363 Kif18a kinesin family member 18A gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20151126 MGI PMID:16822657 1319363 Kif18a kinesin family member 18A gene MP:0001127 small ovary IAGP N RGD:5509061 20151126 MGI PMID:16822657 1319363 Kif18a kinesin family member 18A gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:20981276 1319363 Kif18a kinesin family member 18A gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:20981276 1319363 Kif18a kinesin family member 18A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20151126 MGI PMID:12855593 1319363 Kif18a kinesin family member 18A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20151126 MGI PMID:16822657 1319363 Kif18a kinesin family member 18A gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:20981276 1319363 Kif18a kinesin family member 18A gene MP:0001924 infertility IAGP N RGD:5509061 20151126 MGI PMID:12855593 1319363 Kif18a kinesin family member 18A gene MP:0001924 infertility IAGP N RGD:5509061 20151126 MGI PMID:16822657 1319363 Kif18a kinesin family member 18A gene MP:0001924 infertility IAGP N RGD:5509061 20160623 MGI PMID:25824710 1319363 Kif18a kinesin family member 18A gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20981276 1319363 Kif18a kinesin family member 18A gene MP:0001925 male infertility IAGP N RGD:5509061 20151126 MGI PMID:16822657 1319363 Kif18a kinesin family member 18A gene MP:0001926 female infertility IAGP N RGD:5509061 20151126 MGI PMID:16822657 1319363 Kif18a kinesin family member 18A gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20151126 MGI PMID:12855593 1319363 Kif18a kinesin family member 18A gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20151126 MGI PMID:12855593 1319363 Kif18a kinesin family member 18A gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20151126 MGI PMID:16822657 1319363 Kif18a kinesin family member 18A gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20160623 MGI PMID:25824710 1319363 Kif18a kinesin family member 18A gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:20981276 1319363 Kif18a kinesin family member 18A gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:20981276 1319363 Kif18a kinesin family member 18A gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:20981276 1319363 Kif18a kinesin family member 18A gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20160623 MGI PMID:25824710 1319363 Kif18a kinesin family member 18A gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20981276 1319363 Kif18a kinesin family member 18A gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20160623 MGI PMID:25824710 1319363 Kif18a kinesin family member 18A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:20981276 1319363 Kif18a kinesin family member 18A gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20151126 MGI PMID:16822657 1319363 Kif18a kinesin family member 18A gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20151126 MGI PMID:16822657 1319363 Kif18a kinesin family member 18A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20160623 MGI PMID:25824710 1319363 Kif18a kinesin family member 18A gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20160623 MGI PMID:25824710 1319363 Kif18a kinesin family member 18A gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20160623 MGI PMID:25824710 1319363 Kif18a kinesin family member 18A gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:20981276 1319363 Kif18a kinesin family member 18A gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20151126 MGI PMID:16822657 1319363 Kif18a kinesin family member 18A gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20151126 MGI PMID:16822657 1319363 Kif18a kinesin family member 18A gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20160623 MGI PMID:25824710 1319363 Kif18a kinesin family member 18A gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20160623 MGI PMID:25824710 1319363 Kif18a kinesin family member 18A gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20151126 MGI PMID:16822657 1319363 Kif18a kinesin family member 18A gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20160623 MGI PMID:25824710 1319363 Kif18a kinesin family member 18A gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:20981276 1319363 Kif18a kinesin family member 18A gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20200130 MGI PMID:16822657 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0003155 abnormal telomere length IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319365 Ctc1 CTS telomere maintenance complex component 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22531781 1319367 Rgr retinal G protein coupled receptor gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:11431696 1319367 Rgr retinal G protein coupled receptor gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11431696 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0004024 aneuploidy IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0004025 polyploidy IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0005331 insulin resistance IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319369 Mad2l1bp MAD2L1 binding protein gene MP:0030951 abnormal endocytosis IAGP N RGD:5509061 20211118 MGI PMID:27374329 1319371 Erp44 endoplasmic reticulum protein 44 gene MP:0001192 scaly skin IEA N RGD:5509061 20141003 MGI 1319371 Erp44 endoplasmic reticulum protein 44 gene MP:0001255 decreased body height IEA N RGD:5509061 20141003 MGI 1319371 Erp44 endoplasmic reticulum protein 44 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20141003 MGI 1319371 Erp44 endoplasmic reticulum protein 44 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150108 MGI 1319371 Erp44 endoplasmic reticulum protein 44 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 1319371 Erp44 endoplasmic reticulum protein 44 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1319372 Glis2 GLIS family zinc finger 2 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:17618285 1319372 Glis2 GLIS family zinc finger 2 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17618285 1319372 Glis2 GLIS family zinc finger 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17618285 1319372 Glis2 GLIS family zinc finger 2 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:17618285 1319372 Glis2 GLIS family zinc finger 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17618285 1319372 Glis2 GLIS family zinc finger 2 gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:17618285 1319372 Glis2 GLIS family zinc finger 2 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319372 Glis2 GLIS family zinc finger 2 gene MP:0011422 kidney medulla atrophy IAGP N RGD:5509061 20141003 MGI PMID:17618285 1319372 Glis2 GLIS family zinc finger 2 gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20141003 MGI PMID:17618285 1319372 Glis2 GLIS family zinc finger 2 gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:18227149 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20210715 MGI PMID:33899734 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20210715 MGI PMID:33899734 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0002892 decreased superior colliculus size IAGP N RGD:5509061 20210715 MGI PMID:33899734 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20210715 MGI PMID:33899734 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20210715 MGI PMID:33899734 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0008758 abnormal T cell receptor beta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20210715 MGI PMID:33899734 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20210715 MGI PMID:33899734 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0009960 abnormal cerebellum anterior lobe morphology IAGP N RGD:5509061 20210715 MGI PMID:33899734 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18483223 1319374 Upf2 UPF2 regulator of nonsense transcripts homolog (yeast) gene MP:0020393 increased neuronal precursor proliferation IAGP N RGD:5509061 20210715 MGI PMID:33899734 1319376 Hoxd1 homeobox D1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:21151121 1319376 Hoxd1 homeobox D1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21151121 1319376 Hoxd1 homeobox D1 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:21151121 1319376 Hoxd1 homeobox D1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11511348 1319376 Hoxd1 homeobox D1 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:11511348 1319376 Hoxd1 homeobox D1 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:11511348 1319376 Hoxd1 homeobox D1 gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20141003 MGI PMID:11511348 1319376 Hoxd1 homeobox D1 gene MP:0010729 absent arcus anterior IAGP N RGD:5509061 20141003 MGI PMID:11511348 1319376 Hoxd1 homeobox D1 gene MP:0010730 absent odontoid process IAGP N RGD:5509061 20141003 MGI PMID:11511348 1319376 Hoxd1 homeobox D1 gene MP:0014488 abnormal skin sensory neuron innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:21151121 1319380 Shc4 SHC (Src homology 2 domain containing) family, member 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 1319382 Anks1 ankyrin repeat and SAM domain containing 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20221215 MGI 1319382 Anks1 ankyrin repeat and SAM domain containing 1 gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20221215 MGI 1319382 Anks1 ankyrin repeat and SAM domain containing 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20230601 MGI 1319382 Anks1 ankyrin repeat and SAM domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20100865 1319382 Anks1 ankyrin repeat and SAM domain containing 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1319382 Anks1 ankyrin repeat and SAM domain containing 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1319382 Anks1 ankyrin repeat and SAM domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1319382 Anks1 ankyrin repeat and SAM domain containing 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1319387 Mastl microtubule associated serine/threonine kinase-like gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:24101512 1319387 Mastl microtubule associated serine/threonine kinase-like gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24101512 1319387 Mastl microtubule associated serine/threonine kinase-like gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:24101512 1319387 Mastl microtubule associated serine/threonine kinase-like gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24101512 1319387 Mastl microtubule associated serine/threonine kinase-like gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:24101512 1319389 Bri3 brain protein I3 gene MP:0001314 cornea opacity IEA N RGD:5509061 20201231 MGI 1319393 Msh4 mutS homolog 4 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:10809667 1319393 Msh4 mutS homolog 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10809667 1319393 Msh4 mutS homolog 4 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10809667 1319393 Msh4 mutS homolog 4 gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10809667 1319393 Msh4 mutS homolog 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10809667 1319393 Msh4 mutS homolog 4 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:10809667 1319393 Msh4 mutS homolog 4 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:10809667 1319393 Msh4 mutS homolog 4 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:10809667 1319396 Sdsl serine dehydratase-like gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20181227 MGI 1319396 Sdsl serine dehydratase-like gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1319396 Sdsl serine dehydratase-like gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20190502 MGI 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22644989 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22644989 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22644989 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22644989 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22644989 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:22644989 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22644989 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20160714 MGI PMID:18272476 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20160714 MGI PMID:18272476 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20171012 MGI PMID:26232227 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22644989 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22644989 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22644989 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20150924 MGI PMID:26232227 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22644989 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:15248865 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:26232227 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:15248865 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:15248865 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:15248865 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0020474 advanced circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:15248865 1319400 Zfhx3 zinc finger homeobox 3 gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:15248865 1319402 Malt1 MALT1 paracaspase gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20201022 MGI PMID:32343482 1319402 Malt1 MALT1 paracaspase gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:14576442 1319402 Malt1 MALT1 paracaspase gene MP:0001193 psoriasis IAGP N RGD:5509061 20201022 MGI PMID:32343482 1319402 Malt1 MALT1 paracaspase gene MP:0001219 thick epidermis IAGP N RGD:5509061 20201022 MGI PMID:32343482 1319402 Malt1 MALT1 paracaspase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201022 MGI PMID:32343482 1319402 Malt1 MALT1 paracaspase gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:14614861 1319402 Malt1 MALT1 paracaspase gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:14614861 1319402 Malt1 MALT1 paracaspase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14576442 1319402 Malt1 MALT1 paracaspase gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14576442 1319402 Malt1 MALT1 paracaspase gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:14576442 1319402 Malt1 MALT1 paracaspase gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16862125 1319402 Malt1 MALT1 paracaspase gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14576442 1319402 Malt1 MALT1 paracaspase gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14576442 1319402 Malt1 MALT1 paracaspase gene MP:0004947 skin inflammation IAGP N RGD:5509061 20201022 MGI PMID:32343482 1319402 Malt1 MALT1 paracaspase gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14576442 1319402 Malt1 MALT1 paracaspase gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14614861 1319402 Malt1 MALT1 paracaspase gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20201022 MGI PMID:32343482 1319402 Malt1 MALT1 paracaspase gene MP:0008203 absent B-1a cells IAGP N RGD:5509061 20141003 MGI PMID:14576442 1319402 Malt1 MALT1 paracaspase gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:14576442 1319402 Malt1 MALT1 paracaspase gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20150702 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0000140 absent vertebral pedicles IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0000153 rib bifurcation IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0000154 rib fusion IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0000161 scoliosis IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0000297 abnormal atrioventricular cushion morphology IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0000489 abnormal large intestine morphology IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0000534 abnormal ureter morphology IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0002989 small kidney IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0003345 decreased rib number IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0004442 occipital bone foramen IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0004646 decreased cervical vertebrae number IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0010602 abnormal pulmonary valve cusp morphology IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0013913 absent costovertebral joint IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0013914 absent intracranial segment of vertebral artery IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0013968 multiple persisting craniopharyngeal ducts IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0014003 additional anastomosis between intracranial vertebral arteries IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1319407 Cir1 corepressor interacting with RBPJ, 1 gene MP:0020500 persistent trigeminal artery IEA N RGD:5509061 20180628 MGI 1319411 Kcnk16 potassium channel, subfamily K, member 16 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20180503 MGI PMID:28928238 1319411 Kcnk16 potassium channel, subfamily K, member 16 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20180503 MGI PMID:28928238 1319411 Kcnk16 potassium channel, subfamily K, member 16 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1319411 Kcnk16 potassium channel, subfamily K, member 16 gene MP:0013277 abnormal fasting circulating glucose level IAGP N RGD:5509061 20180503 MGI PMID:28928238 1319415 Phc1 polyhomeotic 1 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0000080 abnormal exoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11901201 1319415 Phc1 polyhomeotic 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20170817 MGI PMID:11950896 1319415 Phc1 polyhomeotic 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:12122109 1319415 Phc1 polyhomeotic 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11901201 1319415 Phc1 polyhomeotic 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20170817 MGI PMID:11950896 1319415 Phc1 polyhomeotic 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11901201 1319415 Phc1 polyhomeotic 1 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:12122109 1319415 Phc1 polyhomeotic 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0003494 parathyroid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0004342 scapular bone foramen IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0004441 small occipital bone IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11901201 1319415 Phc1 polyhomeotic 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:12122109 1319415 Phc1 polyhomeotic 1 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0006338 abnormal second pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20170817 MGI PMID:11950896 1319415 Phc1 polyhomeotic 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20170817 MGI PMID:11950896 1319415 Phc1 polyhomeotic 1 gene MP:0010428 abnormal heart right ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0010458 pulmonary trunk hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0010568 abnormal bulbus cordis morphology IAGP N RGD:5509061 20141003 MGI PMID:12122109 1319415 Phc1 polyhomeotic 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0012062 small tail bud IAGP N RGD:5509061 20141003 MGI PMID:16024804 1319415 Phc1 polyhomeotic 1 gene MP:0013545 cleft hard palate IAGP N RGD:5509061 20221201 MGI PMID:9367423 1319415 Phc1 polyhomeotic 1 gene MP:0021210 bilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:9367423 1319418 Ccnt2 cyclin T2 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1319418 Ccnt2 cyclin T2 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1319418 Ccnt2 cyclin T2 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1319418 Ccnt2 cyclin T2 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210520 MGI 1319418 Ccnt2 cyclin T2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1319418 Ccnt2 cyclin T2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19364821 1319418 Ccnt2 cyclin T2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1319418 Ccnt2 cyclin T2 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20201231 MGI 1319418 Ccnt2 cyclin T2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:16129705 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:16129705 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16129705 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16129705 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16129705 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:16129705 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:16129705 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16129705 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:16129705 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:16129705 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16129705 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16129705 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16129705 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:16129705 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:16129705 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1319422 Ppp2r3c protein phosphatase 2, regulatory subunit B'', gamma gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230119 MGI 1319425 Ccni cyclin I gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:16847066 1319425 Ccni cyclin I gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:16847066 1319425 Ccni cyclin I gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16847066 1319425 Ccni cyclin I gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16847066 1319425 Ccni cyclin I gene MP:0011282 increased podocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16847066 1319425 Ccni cyclin I gene MP:0011369 increased renal glomerulus apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16847066 1319425 Ccni cyclin I gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20141003 MGI PMID:16847066 1319427 Grtp1 GH regulated TBC protein 1 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20160811 MGI 1319427 Grtp1 GH regulated TBC protein 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20160811 MGI 1319427 Grtp1 GH regulated TBC protein 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1319427 Grtp1 GH regulated TBC protein 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1319428 Cdt1 chromatin licensing and DNA replication factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151217 MGI PMID:23817338 1319433 Rars1 arginyl-tRNA synthetase 1 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20160804 MGI 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18281280 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:18196599 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18196599 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17405882 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17405882 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17405882 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18196599 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:17405882 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:17405882 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:17405882 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:17405882 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17405882 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16807321 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:17405882 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18196599 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18196599 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17405882 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18196599 1319438 Hs6st1 heparan sulfate 6-O-sulfotransferase 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17405882 1319439 Ctdspl2 CTD small phosphatase like 2 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1319439 Ctdspl2 CTD small phosphatase like 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20190502 MGI 1319439 Ctdspl2 CTD small phosphatase like 2 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1319439 Ctdspl2 CTD small phosphatase like 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1319439 Ctdspl2 CTD small phosphatase like 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20240801 MGI PMID:38769918 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20240801 MGI PMID:38769918 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20240801 MGI PMID:38769918 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20201002 MGI PMID:32541879 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20201002 MGI PMID:32541879 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20240801 MGI PMID:38769918 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20240801 MGI PMID:38769918 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20240801 MGI PMID:38769918 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20240801 MGI PMID:38769918 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20201002 MGI PMID:32541879 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20201002 MGI PMID:32541879 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20241017 MGI PMID:38769918 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20240801 MGI PMID:38769918 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20240801 MGI PMID:38769918 1319440 Kansl3 KAT8 regulatory NSL complex subunit 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23219391 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20111116 MGI 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0000706 small thymus IEA N RGD:5509061 20111116 MGI 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:12065839 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9885898 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11751756 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12065839 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9843989 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20150618 MGI PMID:15655112 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0002064 seizures IEA N RGD:5509061 20111116 MGI 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23267019 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11751756 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16878135 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23267019 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:12065839 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22761313 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:23267019 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:23267019 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11751756 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12391195 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:23219391 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23267019 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9885898 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:9843989 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23267019 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9843989 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9885898 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:23267019 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0006413 increased T cell apoptosis IEA N RGD:5509061 20111116 MGI 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9843989 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:18209052 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:9885898 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190606 MGI 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23267019 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190606 MGI 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20190606 MGI 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:23267019 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12391195 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0009787 increased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23219391 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23267019 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20150618 MGI PMID:15655112 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20190606 MGI 1319443 Cd3e CD3 antigen, epsilon polypeptide gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20190606 MGI 1319445 Gng12 guanine nucleotide binding protein (G protein), gamma 12 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20240523 MGI 1319445 Gng12 guanine nucleotide binding protein (G protein), gamma 12 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20240523 MGI 1319445 Gng12 guanine nucleotide binding protein (G protein), gamma 12 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20231207 MGI 1319445 Gng12 guanine nucleotide binding protein (G protein), gamma 12 gene MP:0010052 increased grip strength IEA N RGD:5509061 20231207 MGI 1319449 Eif4a2 eukaryotic translation initiation factor 4A2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1319449 Eif4a2 eukaryotic translation initiation factor 4A2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0000129 ameloblast degeneration IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20240523 MGI 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20240523 MGI 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20240523 MGI 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001147 small testis IEA N RGD:5509061 20240523 MGI 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170608 MGI PMID:26880786 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001426 polydipsia IAGP N RGD:5509061 20170608 MGI PMID:26880786 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20170608 MGI PMID:26880786 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20240523 MGI 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20170608 MGI PMID:26880786 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20240523 MGI 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0003883 enlarged stomach IEA N RGD:5509061 20240523 MGI 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0003948 abnormal gas homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20240523 MGI 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20240523 MGI 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20170608 MGI PMID:26880786 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20170608 MGI PMID:26880786 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20170608 MGI PMID:26880786 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20170608 MGI PMID:26880786 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20170608 MGI PMID:26880786 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20141003 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20170608 MGI PMID:26880786 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:19187773 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0013249 adipose tissue necrosis IAGP N RGD:5509061 20161117 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0030542 abnormal dentin development IAGP N RGD:5509061 20180215 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0030827 femur fracture IAGP N RGD:5509061 20181018 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21051554 1319454 Agpat2 1-acylglycerol-3-phosphate O-acyltransferase 2 gene MP:0031603 brown adipose tissue inflammation IAGP N RGD:5509061 20240321 MGI PMID:21051554 1319456 Wdr33 WD repeat domain 33 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1319456 Wdr33 WD repeat domain 33 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230119 MGI 1319456 Wdr33 WD repeat domain 33 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1319456 Wdr33 WD repeat domain 33 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230119 MGI 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000433 microcephaly IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000601 small liver IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000603 pale liver IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10469594 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0003943 abnormal hepatobiliary system development IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0004385 interparietal bone hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0004420 parietal bone hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0004424 temporal bone hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0004444 small supraoccipital bone IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0004455 pterygoid bone hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0004461 basisphenoid bone hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16940357 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0006306 abnormal nasal pit morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16940357 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16940357 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0008797 facial cleft IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0008991 abnormal bile canaliculus morphology IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:10469594 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0009891 abnormal palate bone morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0009913 abnormal hyoid bone greater horn morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141218 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10469594 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0012090 midbrain hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0012129 failure of blastocyst formation IAGP N RGD:5509061 20141003 MGI PMID:10469594 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0012139 increased forebrain size IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0012754 abnormal cranial neural crest cell morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0012760 decreased cranial neural crest cell proliferation IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:23299886 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0030112 zygomatic bone hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0030119 abnormal retrotympanic process morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0030261 abnormal temporal bone zygomatic process morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0030285 mandibular coronoid process hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0030301 abnormal maxillary frontal process morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0030374 Meckel's cartilage hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0030386 facial bone hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0030869 thyroid cartilage hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0030874 cricoid cartilage hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0031454 decreased cranial neural crest cell apoptosis IAGP N RGD:5509061 20221110 MGI PMID:34184034 1319460 Srsf3 serine and arginine-rich splicing factor 3 gene MP:0031459 maxillary zygomatic process hypoplasia IAGP N RGD:5509061 20221201 MGI PMID:34184034 1319462 Uap1 UDP-N-acetylglucosamine pyrophosphorylase 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230119 MGI 1319462 Uap1 UDP-N-acetylglucosamine pyrophosphorylase 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1319462 Uap1 UDP-N-acetylglucosamine pyrophosphorylase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1319462 Uap1 UDP-N-acetylglucosamine pyrophosphorylase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230119 MGI 1319464 Zc3hav1l zinc finger CCCH-type, antiviral 1-like gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20181227 MGI 1319464 Zc3hav1l zinc finger CCCH-type, antiviral 1-like gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1319464 Zc3hav1l zinc finger CCCH-type, antiviral 1-like gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20231207 MGI 1319466 Tle1 transducin-like enhancer of split 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1319466 Tle1 transducin-like enhancer of split 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20240523 MGI 1319471 Spmap2 sperm microtubule associated protein 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12748127 1319471 Spmap2 sperm microtubule associated protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10747865 1319471 Spmap2 sperm microtubule associated protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12748127 1319471 Spmap2 sperm microtubule associated protein 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10747865 1319471 Spmap2 sperm microtubule associated protein 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10747865 1319471 Spmap2 sperm microtubule associated protein 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10747865 1319471 Spmap2 sperm microtubule associated protein 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:10747865 1319471 Spmap2 sperm microtubule associated protein 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10747865 1319471 Spmap2 sperm microtubule associated protein 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:10747865 1319471 Spmap2 sperm microtubule associated protein 2 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:10747865 1319471 Spmap2 sperm microtubule associated protein 2 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10747865 1319471 Spmap2 sperm microtubule associated protein 2 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:10747865 1319471 Spmap2 sperm microtubule associated protein 2 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20141003 MGI PMID:10747865 1319472 Eif1b eukaryotic translation initiation factor 1B gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1319472 Eif1b eukaryotic translation initiation factor 1B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1319474 Rnmt RNA (guanine-7-) methyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319474 Rnmt RNA (guanine-7-) methyltransferase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1319474 Rnmt RNA (guanine-7-) methyltransferase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1319476 Calr3 calreticulin 3 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:21131354 1319476 Calr3 calreticulin 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21131354 1319476 Calr3 calreticulin 3 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20200102 MGI PMID:21131354 1319476 Calr3 calreticulin 3 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220303 MGI PMID:21131354 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20141009 MGI 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20200402 MGI 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20141003 MGI 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20141003 MGI 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0001304 cataract IEA N RGD:5509061 20141003 MGI 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0001307 fused cornea and lens IEA N RGD:5509061 20160114 MGI 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20160114 MGI 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0001314 cornea opacity IEA N RGD:5509061 20170105 MGI 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20160114 MGI 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20201231 MGI 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20211021 MGI 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20201231 MGI 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1319478 Agap1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20201231 MGI 1319480 Unc5d unc-5 netrin receptor D gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:21673655 1319480 Unc5d unc-5 netrin receptor D gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:21673655 1319484 Tjp3 tight junction protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17000770 1319484 Tjp3 tight junction protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18172007 1319486 Sdhaf4 succinate dehydrogenase complex assembly factor 4 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20240307 MGI PMID:35803927 1319486 Sdhaf4 succinate dehydrogenase complex assembly factor 4 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20240307 MGI PMID:35803927 1319486 Sdhaf4 succinate dehydrogenase complex assembly factor 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240307 MGI PMID:35803927 1319486 Sdhaf4 succinate dehydrogenase complex assembly factor 4 gene MP:0002083 premature death IAGP N RGD:5509061 20240307 MGI PMID:35803927 1319486 Sdhaf4 succinate dehydrogenase complex assembly factor 4 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20240307 MGI PMID:35803927 1319486 Sdhaf4 succinate dehydrogenase complex assembly factor 4 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20240307 MGI PMID:35803927 1319486 Sdhaf4 succinate dehydrogenase complex assembly factor 4 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20240307 MGI PMID:35803927 1319486 Sdhaf4 succinate dehydrogenase complex assembly factor 4 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20240307 MGI PMID:35803927 1319486 Sdhaf4 succinate dehydrogenase complex assembly factor 4 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20240307 MGI PMID:35803927 1319486 Sdhaf4 succinate dehydrogenase complex assembly factor 4 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20240307 MGI PMID:35803927 1319486 Sdhaf4 succinate dehydrogenase complex assembly factor 4 gene MP:0010656 thick myocardium IAGP N RGD:5509061 20240307 MGI PMID:35803927 1319486 Sdhaf4 succinate dehydrogenase complex assembly factor 4 gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20240307 MGI PMID:35803927 1319486 Sdhaf4 succinate dehydrogenase complex assembly factor 4 gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240307 MGI PMID:35803927 1319486 Sdhaf4 succinate dehydrogenase complex assembly factor 4 gene MP:0014390 decreased myocardial fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:35803927 1319486 Sdhaf4 succinate dehydrogenase complex assembly factor 4 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:35803927 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18200042 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19801644 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18200042 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20150611 MGI PMID:25660120 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:19801644 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20150611 MGI PMID:25660120 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20150611 MGI PMID:25660120 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18200042 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20150611 MGI PMID:25660120 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20150611 MGI PMID:25660120 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20150611 MGI PMID:25660120 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20150611 MGI PMID:25660120 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18200042 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20150611 MGI PMID:25660120 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20150611 MGI PMID:25660120 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:19801644 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0008109 abnormal small intestinal microvillus morphology IAGP N RGD:5509061 20141003 MGI PMID:19801644 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20150611 MGI PMID:25660120 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19801644 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19801644 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19801644 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18200042 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19801644 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0011198 absent proamniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:18200042 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20150611 MGI PMID:25660120 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20150611 MGI PMID:25660120 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0011637 abnormal mitochondrial matrix morphology IAGP N RGD:5509061 20150611 MGI PMID:25660120 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20150611 MGI PMID:25660120 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:18200042 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:18200042 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0014079 decreased small intestinal villus number IAGP N RGD:5509061 20160414 MGI PMID:19801644 1319488 Gadd45gip1 growth arrest and DNA-damage-inducible, gamma interacting protein 1 gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20160414 MGI PMID:19801644 1319490 Slc30a6 solute carrier family 30 (zinc transporter), member 6 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20231207 MGI 1319492 1600014C10Rik RIKEN cDNA 1600014C10 gene gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1319492 1600014C10Rik RIKEN cDNA 1600014C10 gene gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1319497 Trmt10a tRNA methyltransferase 10A gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 1319497 Trmt10a tRNA methyltransferase 10A gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1319497 Trmt10a tRNA methyltransferase 10A gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1319497 Trmt10a tRNA methyltransferase 10A gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160804 MGI 1319497 Trmt10a tRNA methyltransferase 10A gene MP:0001304 cataract IEA N RGD:5509061 20160804 MGI 1319497 Trmt10a tRNA methyltransferase 10A gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20160804 MGI 1319497 Trmt10a tRNA methyltransferase 10A gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1319497 Trmt10a tRNA methyltransferase 10A gene MP:0003443 increased circulating glycerol level IEA N RGD:5509061 20160804 MGI 1319497 Trmt10a tRNA methyltransferase 10A gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1319497 Trmt10a tRNA methyltransferase 10A gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 1319497 Trmt10a tRNA methyltransferase 10A gene MP:0010092 increased circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:23870131 1319497 Trmt10a tRNA methyltransferase 10A gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20160804 MGI 1319499 Zmiz2 zinc finger, MIZ-type containing 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1319499 Zmiz2 zinc finger, MIZ-type containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319499 Zmiz2 zinc finger, MIZ-type containing 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1319499 Zmiz2 zinc finger, MIZ-type containing 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1319505 Dnali1 dynein, axonemal, light intermediate polypeptide 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20231102 MGI PMID:36792588 1319505 Dnali1 dynein, axonemal, light intermediate polypeptide 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20231102 MGI PMID:36792588 1319505 Dnali1 dynein, axonemal, light intermediate polypeptide 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20231102 MGI PMID:36792588 1319505 Dnali1 dynein, axonemal, light intermediate polypeptide 1 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20231102 MGI PMID:36792588 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:14625273 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10085069 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:14625273 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:14625273 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:14625273 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14625273 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:14625273 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:14625273 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:14625273 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:14625273 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:14625273 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:21555557 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200116 MGI PMID:21555557 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10085069 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10085069 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:21555557 1319507 Rce1 Ras converting CAAX endopeptidase 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:21555557 1319510 Tmco6 transmembrane and coiled-coil domains 6 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20240523 MGI 1319510 Tmco6 transmembrane and coiled-coil domains 6 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 1319510 Tmco6 transmembrane and coiled-coil domains 6 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20240523 MGI 1319510 Tmco6 transmembrane and coiled-coil domains 6 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20240523 MGI 1319510 Tmco6 transmembrane and coiled-coil domains 6 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20240523 MGI 1319510 Tmco6 transmembrane and coiled-coil domains 6 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1319510 Tmco6 transmembrane and coiled-coil domains 6 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1319510 Tmco6 transmembrane and coiled-coil domains 6 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1319510 Tmco6 transmembrane and coiled-coil domains 6 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20240523 MGI 1319510 Tmco6 transmembrane and coiled-coil domains 6 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22228099 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22228099 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0001260 increased body weight IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0001261 obese IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20150521 MGI PMID:22228099 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:22228099 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0004574 broad limb buds IAGP N RGD:5509061 20150521 MGI PMID:22228099 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210520 MGI 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:22228099 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22228099 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0011939 increased food intake IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0012531 delayed limb development IAGP N RGD:5509061 20150521 MGI PMID:22228099 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20160211 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0030964 decreased brain ependyma motile cilium length IAGP N RGD:5509061 20190725 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0030966 decreased brain ependyma motile cilium number IAGP N RGD:5509061 20190725 MGI PMID:23572516 1319512 Bbs7 Bardet-Biedl syndrome 7 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220317 MGI PMID:23572516 1319515 Tmem131 transmembrane protein 131 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20220519 MGI 1319515 Tmem131 transmembrane protein 131 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1319515 Tmem131 transmembrane protein 131 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20220519 MGI 1319515 Tmem131 transmembrane protein 131 gene MP:0001785 edema IEA N RGD:5509061 20220519 MGI 1319515 Tmem131 transmembrane protein 131 gene MP:0001914 hemorrhage IEA N RGD:5509061 20220519 MGI 1319515 Tmem131 transmembrane protein 131 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1319515 Tmem131 transmembrane protein 131 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1319515 Tmem131 transmembrane protein 131 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1319515 Tmem131 transmembrane protein 131 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1319517 Cstf1 cleavage stimulation factor, 3' pre-RNA, subunit 1 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20230601 MGI 1319517 Cstf1 cleavage stimulation factor, 3' pre-RNA, subunit 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:19815519 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000413 polyphalangy IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:12361967 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19056373 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20210114 MGI PMID:32702291 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:15496441 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:15496441 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000867 abnormal cerebellum anterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:15496441 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:12361967 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12361967 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19056373 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20210114 MGI PMID:32702291 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12361967 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:14723851 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21337666 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22698544 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:14723851 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:19666503 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20210114 MGI PMID:32702291 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:14723851 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21337666 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:14723851 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:15215207 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:12361967 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:14723851 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20180927 MGI PMID:29999500 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21337666 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20180215 MGI PMID:28817564 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0001958 emphysema IAGP N RGD:5509061 20180927 MGI PMID:29999500 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16914490 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:14723851 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19056373 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19549984 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19666503 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21209331 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22549777 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20180215 MGI PMID:28817564 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20180927 MGI PMID:29999500 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:14723851 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0003159 abnormal esophageal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0003160 abnormal esophagus development IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0003276 esophageal atresia IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:12361967 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:19056373 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004100 abnormal spinal cord interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004544 absent esophagus IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004711 persistence of notochord tissue IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004711 persistence of notochord tissue IAGP N RGD:5509061 20141003 MGI PMID:12361967 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004790 absent upper incisors IAGP N RGD:5509061 20170928 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004791 absent lower incisors IAGP N RGD:5509061 20170928 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:14723851 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004979 abnormal neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:14723851 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:14723851 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:12361967 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0005315 absent pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19815519 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0009199 abnormal external male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0009569 abnormal left lung morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0009570 abnormal right lung morphology IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0009571 abnormal right lung accessory lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0009572 abnormal right lung cranial lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:15496441 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:14723851 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16950124 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0010811 decreased type II pneumocyte number IAGP N RGD:5509061 20180927 MGI PMID:29999500 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0010824 absent right lung accessory lobe IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0010827 small lung saccule IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0010828 abnormal bronchioalveolar stem cell morphology IAGP N RGD:5509061 20180927 MGI PMID:29999500 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0010881 esophagus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0010882 trachea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0010883 trachea stenosis IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0010884 esophagus stenosis IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0010885 absent trachea IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0010906 abnormal lung bud morphology IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011011 impaired lung lobe morphogenesis IAGP N RGD:5509061 20200917 MGI PMID:12361967 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14723851 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15496441 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16571625 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19056373 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12361967 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16914490 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10725236 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011148 decreased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20141003 MGI PMID:9006072 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20210114 MGI PMID:32702291 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0013496 abnormal trachea development IAGP N RGD:5509061 20150212 MGI PMID:9731531 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0013785 abnormal mammary gland bud morphology IAGP N RGD:5509061 20150611 MGI PMID:16914490 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0021101 abnormal ventral interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:14723851 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0021101 abnormal ventral interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:15215207 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0021102 abnormal ventral interneuron 0 morphology IAGP N RGD:5509061 20220310 MGI PMID:15215207 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0021103 abnormal ventral interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:15215207 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:15215207 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:11748151 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:12361967 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:14723851 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:15215207 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0030255 abnormal maxillary dental arch morphology IAGP N RGD:5509061 20171019 MGI PMID:19056373 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0030258 small mandibular condyloid process IAGP N RGD:5509061 20171019 MGI PMID:19815519 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0030301 abnormal maxillary frontal process morphology IAGP N RGD:5509061 20171102 MGI PMID:19056373 1319523 Gli2 GLI-Kruppel family member GLI2 gene MP:0030331 absent temporomandibular joint disk IAGP N RGD:5509061 20171109 MGI PMID:19815519 1319525 Kcnv2 potassium channel, subfamily V, member 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141030 MGI 1319525 Kcnv2 potassium channel, subfamily V, member 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200116 MGI PMID:30820446 1319525 Kcnv2 potassium channel, subfamily V, member 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200116 MGI PMID:30820446 1319525 Kcnv2 potassium channel, subfamily V, member 2 gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20200116 MGI PMID:30820446 1319525 Kcnv2 potassium channel, subfamily V, member 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:30820446 1319525 Kcnv2 potassium channel, subfamily V, member 2 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20200116 MGI PMID:30820446 1319525 Kcnv2 potassium channel, subfamily V, member 2 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200116 MGI PMID:30820446 1319525 Kcnv2 potassium channel, subfamily V, member 2 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200116 MGI PMID:30820446 1319525 Kcnv2 potassium channel, subfamily V, member 2 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20200116 MGI PMID:30820446 1319526 Sall2 spalt like transcription factor 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:12482961 1319526 Sall2 spalt like transcription factor 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18818376 1319526 Sall2 spalt like transcription factor 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:18818376 1319526 Sall2 spalt like transcription factor 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18818376 1319526 Sall2 spalt like transcription factor 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12482961 1319526 Sall2 spalt like transcription factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12482961 1319526 Sall2 spalt like transcription factor 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:12482961 1319526 Sall2 spalt like transcription factor 2 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:12482961 1319526 Sall2 spalt like transcription factor 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12482961 1319526 Sall2 spalt like transcription factor 2 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:12482961 1319526 Sall2 spalt like transcription factor 2 gene MP:0004838 abnormal neural fold elevation formation IAGP N RGD:5509061 20141003 MGI PMID:18818376 1319526 Sall2 spalt like transcription factor 2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12482961 1319526 Sall2 spalt like transcription factor 2 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:12482961 1319526 Sall2 spalt like transcription factor 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12482961 1319526 Sall2 spalt like transcription factor 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20150305 MGI PMID:18818376 1319526 Sall2 spalt like transcription factor 2 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18818376 1319532 Slc7a11 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:16144837 1319532 Slc7a11 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 gene MP:0000371 diluted coat color IEA N RGD:5509061 20111116 MGI 1319532 Slc7a11 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20308543 1319532 Slc7a11 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20308543 1319532 Slc7a11 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20201231 MGI 1319532 Slc7a11 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:20308543 1319532 Slc7a11 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:8699821 1319532 Slc7a11 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1319532 Slc7a11 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:16144837 1319532 Slc7a11 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20201022 MGI 1319532 Slc7a11 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:8699821 1319532 Slc7a11 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20210826 MGI 1319532 Slc7a11 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:16144837 1319532 Slc7a11 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20308543 1319532 Slc7a11 solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 gene MP:0030625 increased circulating cysteine level IAGP N RGD:5509061 20180920 MGI PMID:16144837 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191128 MGI 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0003087 absent allantois IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20181227 MGI 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0012724 absent head fold IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191128 MGI 1319535 Mrpl22 mitochondrial ribosomal protein L22 gene MP:0014246 decreased cellular ATP level IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20940150 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18434326 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18434326 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:18467430 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:18467430 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18467430 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18467430 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18434326 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18467430 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:20940150 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18467430 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18434326 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:18467430 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0004100 abnormal spinal cord interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18467430 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:18434326 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:18434326 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:18467430 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0011019 abnormal adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:18434326 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18434326 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18467430 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:18434326 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20141003 MGI PMID:18434326 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20141003 MGI PMID:18467430 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20141003 MGI PMID:20940150 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0014386 decreased muscle fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:20940150 1319539 Tk2 thymidine kinase 2, mitochondrial gene MP:0014390 decreased myocardial fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:20940150 1319541 Rfc5 replication factor C (activator 1) 5 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20230601 MGI 1319541 Rfc5 replication factor C (activator 1) 5 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220519 MGI 1319541 Rfc5 replication factor C (activator 1) 5 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220519 MGI 1319541 Rfc5 replication factor C (activator 1) 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1319541 Rfc5 replication factor C (activator 1) 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0000274 enlarged heart IEA N RGD:5509061 20160811 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0000947 convulsive seizures IEA N RGD:5509061 20201231 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0001258 decreased body length IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0001260 increased body weight IEA N RGD:5509061 20141003 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20211021 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0001513 limb grasping IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0002175 decreased brain weight IEA N RGD:5509061 20220519 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20170105 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20211021 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0002833 increased heart weight IEA N RGD:5509061 20181227 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0003900 shortened QT interval IEA N RGD:5509061 20210826 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220519 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20170105 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20221215 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220519 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20201231 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20190502 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0010571 shortened ST segment IEA N RGD:5509061 20211021 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20160421 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20210128 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20211021 MGI 1319544 Rnf10 ring finger protein 10 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1319548 Gpn1 GPN-loop GTPase 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 1319548 Gpn1 GPN-loop GTPase 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241017 MGI 1319548 Gpn1 GPN-loop GTPase 1 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20240523 MGI 1319548 Gpn1 GPN-loop GTPase 1 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1319548 Gpn1 GPN-loop GTPase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1319548 Gpn1 GPN-loop GTPase 1 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241017 MGI 1319552 Ppp1r12b protein phosphatase 1, regulatory subunit 12B gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20240502 MGI PMID:38224947 1319552 Ppp1r12b protein phosphatase 1, regulatory subunit 12B gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1319552 Ppp1r12b protein phosphatase 1, regulatory subunit 12B gene MP:0001260 increased body weight IAGP N RGD:5509061 20240502 MGI PMID:36889588 1319552 Ppp1r12b protein phosphatase 1, regulatory subunit 12B gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 1319552 Ppp1r12b protein phosphatase 1, regulatory subunit 12B gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20240502 MGI PMID:36889588 1319552 Ppp1r12b protein phosphatase 1, regulatory subunit 12B gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20240502 MGI PMID:36889588 1319552 Ppp1r12b protein phosphatase 1, regulatory subunit 12B gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20240502 MGI PMID:38224947 1319552 Ppp1r12b protein phosphatase 1, regulatory subunit 12B gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20240502 MGI PMID:36889588 1319552 Ppp1r12b protein phosphatase 1, regulatory subunit 12B gene MP:0010580 decreased heart left ventricle size IAGP N RGD:5509061 20240502 MGI PMID:36889588 1319555 Nthl1 nth (endonuclease III)-like 1 (E.coli) gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1319555 Nthl1 nth (endonuclease III)-like 1 (E.coli) gene MP:0000601 small liver IEA N RGD:5509061 20230119 MGI 1319555 Nthl1 nth (endonuclease III)-like 1 (E.coli) gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1319555 Nthl1 nth (endonuclease III)-like 1 (E.coli) gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1319555 Nthl1 nth (endonuclease III)-like 1 (E.coli) gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 1319555 Nthl1 nth (endonuclease III)-like 1 (E.coli) gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 1319555 Nthl1 nth (endonuclease III)-like 1 (E.coli) gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:12093749 1319555 Nthl1 nth (endonuclease III)-like 1 (E.coli) gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20160804 MGI PMID:12167705 1319557 Supt6 SPT6, histone chaperone and transcription elongation factor gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20151203 MGI PMID:26142281 1319558 Toporsl topoisomerase I binding, arginine/serine-rich like gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1319558 Toporsl topoisomerase I binding, arginine/serine-rich like gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1319560 Nacc2 nucleus accumbens associated 2, BEN and BTB (POZ) domain containing gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 1319560 Nacc2 nucleus accumbens associated 2, BEN and BTB (POZ) domain containing gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201022 MGI 1319560 Nacc2 nucleus accumbens associated 2, BEN and BTB (POZ) domain containing gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1319560 Nacc2 nucleus accumbens associated 2, BEN and BTB (POZ) domain containing gene MP:0013406 abnormal epidermal immune compartment IEA N RGD:5509061 20201231 MGI 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:17537792 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23150596 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:24656820 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0003605 fused kidneys IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:23150596 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23150596 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0010980 ectopic ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0010981 abnormal branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0011486 ectopic ureter IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0011760 abnormal ureteric bud tip morphology IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0011761 abnormal ureteric bud trunk morphology IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319562 Spry1 sprouty RTK signaling antagonist 1 gene MP:0011797 blind ureter IAGP N RGD:5509061 20141003 MGI PMID:15691764 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20150430 MGI 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0001304 cataract IEA N RGD:5509061 20150430 MGI 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0010228 decreased transitional stage T3 B cell number IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319567 Ell2 elongation factor for RNA polymerase II 2 gene MP:0020154 impaired humoral immune response IAGP N RGD:5509061 20160929 MGI PMID:25238757 1319572 Mmel1 membrane metallo-endopeptidase-like 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:15121861 1319572 Mmel1 membrane metallo-endopeptidase-like 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15121861 1319572 Mmel1 membrane metallo-endopeptidase-like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15121861 1319579 Cers4 ceramide synthase 4 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20151015 MGI PMID:24738593 1319579 Cers4 ceramide synthase 4 gene MP:0000414 alopecia IAGP N RGD:5509061 20151015 MGI PMID:24738593 1319579 Cers4 ceramide synthase 4 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20151015 MGI PMID:24738593 1319579 Cers4 ceramide synthase 4 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20151015 MGI PMID:24738593 1319579 Cers4 ceramide synthase 4 gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20151015 MGI PMID:24738593 1319579 Cers4 ceramide synthase 4 gene MP:0002992 abnormal sebaceous lipid secretion IAGP N RGD:5509061 20151015 MGI PMID:24738593 1319579 Cers4 ceramide synthase 4 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20151015 MGI PMID:24738593 1319579 Cers4 ceramide synthase 4 gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20151015 MGI PMID:24738593 1319579 Cers4 ceramide synthase 4 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20151015 MGI PMID:24738593 1319579 Cers4 ceramide synthase 4 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20151015 MGI PMID:24738593 1319579 Cers4 ceramide synthase 4 gene MP:0030571 dilated piliary canal IAGP N RGD:5509061 20180524 MGI PMID:24738593 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:15946934 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15946934 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15946934 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14981116 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:15946934 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:15946934 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15946934 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0003883 enlarged stomach IEA N RGD:5509061 20210520 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0005238 increased brain size IEA N RGD:5509061 20210520 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:15946934 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14981116 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15946934 1319581 Spred2 sprouty-related EVH1 domain containing 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19573810 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:21730163 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170831 MGI PMID:17533180 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20170831 MGI PMID:17533180 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21674502 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:23770245 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11528400 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12101245 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16616333 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20962274 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21730163 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21674502 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:19573810 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19573810 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19573810 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12101245 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:12101245 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:21674502 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21674502 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21674502 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0001661 extended life span IAGP N RGD:5509061 20170831 MGI PMID:17533180 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:15361844 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20962274 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12101245 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21730163 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0001785 edema IAGP N RGD:5509061 20170831 MGI PMID:17533180 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20170831 MGI PMID:17533180 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19573810 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16354690 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19573810 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23770245 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0002083 premature death IAGP N RGD:5509061 20170831 MGI PMID:17533180 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16354690 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21730132 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21730163 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170831 MGI PMID:17533180 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003010 decreased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:19573810 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:12101245 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16616333 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19573810 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20170831 MGI PMID:17533180 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:19573810 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20170831 MGI PMID:17533180 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:12101245 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:12101245 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:12101245 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15361844 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20962274 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:21730132 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:12101245 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21730163 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20170831 MGI PMID:17533180 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20170831 MGI PMID:17533180 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:19573810 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20170831 MGI PMID:17533180 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:21730163 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20170831 MGI PMID:17533180 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190221 MGI 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190221 MGI 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0008082 increased single-positive T cell number IEA N RGD:5509061 20190221 MGI 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0008083 decreased single-positive T cell number IEA N RGD:5509061 20190221 MGI 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:12101245 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:21674502 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19573810 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19573810 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16354690 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21674502 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11528400 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12101245 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21730132 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21730163 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12101245 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15361844 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20962274 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:12101245 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:16616333 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19573810 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17526734 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:21730163 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:17533180 1319585 Mdm4 transformed mouse 3T3 cell double minute 4 gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:23770245 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0000601 small liver IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1319588 Ufl1 UFM1 specific ligase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170314 MGI PMID:25952549 1319590 Irx4 Iroquois homeobox 4 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11238910 1319590 Irx4 Iroquois homeobox 4 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11238910 1319590 Irx4 Iroquois homeobox 4 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:11238910 1319590 Irx4 Iroquois homeobox 4 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:11238910 1319590 Irx4 Iroquois homeobox 4 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11238910 1319590 Irx4 Iroquois homeobox 4 gene MP:0008727 increased heart right atrium size IAGP N RGD:5509061 20231221 MGI PMID:11238910 1319590 Irx4 Iroquois homeobox 4 gene MP:0011917 increased heart right atrium weight IAGP N RGD:5509061 20231221 MGI PMID:11238910 1319591 Tmem94 transmembrane protein 94 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1319591 Tmem94 transmembrane protein 94 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0002188 small heart IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 1319591 Tmem94 transmembrane protein 94 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0008443 absent subplate IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0010489 abnormal heart atrium auricular region morphology IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0030245 round head IAGP N RGD:5509061 20190919 MGI PMID:30526868 1319591 Tmem94 transmembrane protein 94 gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:30526868 1319592 Nxnl2 nucleoredoxin-like 2 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20240523 MGI 1319592 Nxnl2 nucleoredoxin-like 2 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20230601 MGI 1319592 Nxnl2 nucleoredoxin-like 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1319592 Nxnl2 nucleoredoxin-like 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1319592 Nxnl2 nucleoredoxin-like 2 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1319592 Nxnl2 nucleoredoxin-like 2 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1319592 Nxnl2 nucleoredoxin-like 2 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230601 MGI 1319592 Nxnl2 nucleoredoxin-like 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1319592 Nxnl2 nucleoredoxin-like 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22343139 1319592 Nxnl2 nucleoredoxin-like 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22343139 1319592 Nxnl2 nucleoredoxin-like 2 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22343139 1319592 Nxnl2 nucleoredoxin-like 2 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:22343139 1319592 Nxnl2 nucleoredoxin-like 2 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:22343139 1319592 Nxnl2 nucleoredoxin-like 2 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:22343139 1319597 Mrps36 mitochondrial ribosomal protein S36 gene MP:0001297 microphthalmia IEA N RGD:5509061 20221215 MGI 1319597 Mrps36 mitochondrial ribosomal protein S36 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20240523 MGI 1319597 Mrps36 mitochondrial ribosomal protein S36 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1319597 Mrps36 mitochondrial ribosomal protein S36 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220811 MGI 1319597 Mrps36 mitochondrial ribosomal protein S36 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1319597 Mrps36 mitochondrial ribosomal protein S36 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1319597 Mrps36 mitochondrial ribosomal protein S36 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1319597 Mrps36 mitochondrial ribosomal protein S36 gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20220811 MGI 1319600 Slc2a6 solute carrier family 2 (facilitated glucose transporter), member 6 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20210617 MGI PMID:30431159 1319600 Slc2a6 solute carrier family 2 (facilitated glucose transporter), member 6 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20210617 MGI PMID:30431159 1319600 Slc2a6 solute carrier family 2 (facilitated glucose transporter), member 6 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20210617 MGI PMID:30431159 1319600 Slc2a6 solute carrier family 2 (facilitated glucose transporter), member 6 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20191010 MGI PMID:29664675 1319600 Slc2a6 solute carrier family 2 (facilitated glucose transporter), member 6 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20191010 MGI PMID:29664675 1319602 Adcy1 adenylate cyclase 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210520 MGI 1319602 Adcy1 adenylate cyclase 1 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:18524897 1319602 Adcy1 adenylate cyclase 1 gene MP:0000861 disorganized barrel cortex IAGP N RGD:5509061 20141003 MGI PMID:8596955 1319602 Adcy1 adenylate cyclase 1 gene MP:0000862 absent barrels in primary somatosensory cortex IAGP N RGD:5509061 20141003 MGI PMID:18524897 1319602 Adcy1 adenylate cyclase 1 gene MP:0000862 absent barrels in primary somatosensory cortex IAGP N RGD:5509061 20141003 MGI PMID:8596955 1319602 Adcy1 adenylate cyclase 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20200402 MGI 1319602 Adcy1 adenylate cyclase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1319602 Adcy1 adenylate cyclase 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20200402 MGI 1319602 Adcy1 adenylate cyclase 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 1319602 Adcy1 adenylate cyclase 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:7816821 1319602 Adcy1 adenylate cyclase 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:10482244 1319602 Adcy1 adenylate cyclase 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10482244 1319602 Adcy1 adenylate cyclase 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18524897 1319602 Adcy1 adenylate cyclase 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1319602 Adcy1 adenylate cyclase 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:16525048 1319602 Adcy1 adenylate cyclase 1 gene MP:0001908 abnormal somatosensory cortex physiology IAGP N RGD:5509061 20141003 MGI PMID:8596955 1319602 Adcy1 adenylate cyclase 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200402 MGI 1319602 Adcy1 adenylate cyclase 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:18524897 1319602 Adcy1 adenylate cyclase 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1319602 Adcy1 adenylate cyclase 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16525048 1319602 Adcy1 adenylate cyclase 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:7816821 1319602 Adcy1 adenylate cyclase 1 gene MP:0003989 abnormal barrel cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18524897 1319602 Adcy1 adenylate cyclase 1 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:10482244 1319602 Adcy1 adenylate cyclase 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20230720 MGI 1319602 Adcy1 adenylate cyclase 1 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:12441059 1319602 Adcy1 adenylate cyclase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:7816821 1319602 Adcy1 adenylate cyclase 1 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:12441059 1319602 Adcy1 adenylate cyclase 1 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 1319602 Adcy1 adenylate cyclase 1 gene MP:0014372 decreased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:18524897 1319605 Top3a topoisomerase (DNA) III alpha gene MP:0004966 abnormal inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:9448276 1319605 Top3a topoisomerase (DNA) III alpha gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20201022 MGI 1319605 Top3a topoisomerase (DNA) III alpha gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9448276 1319605 Top3a topoisomerase (DNA) III alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319605 Top3a topoisomerase (DNA) III alpha gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1319609 Ltk leukocyte tyrosine kinase gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1319609 Ltk leukocyte tyrosine kinase gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 1319609 Ltk leukocyte tyrosine kinase gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20230601 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11956231 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20210930 MGI PMID:33905568 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20210930 MGI PMID:33905568 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15537447 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16293698 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17147489 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20210930 MGI PMID:33905568 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11956231 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15537447 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16293698 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17147489 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:19837033 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19837032 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15537447 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:15537447 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15537447 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000555 absent carpal bone IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:15537447 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:12509515 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000566 synostosis IAGP N RGD:5509061 20141003 MGI PMID:15537447 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:12509515 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17147489 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:11956231 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:11956231 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:15537447 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:16163358 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:19041748 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:21402791 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20161117 MGI PMID:27524797 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20170706 MGI PMID:28356706 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20161117 MGI PMID:27524797 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20230511 MGI PMID:33497368 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20161117 MGI PMID:27524797 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:12509515 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:15537447 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002183 gliosis IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12509515 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18263894 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19154719 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19837033 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20161117 MGI PMID:27524797 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20170706 MGI PMID:28356706 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20160602 MGI PMID:24789067 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17147489 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:12509515 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:19837033 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003074 absent metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003727 abnormal retina layer morphology IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003732 abnormal retina outer plexiform layer morphology IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16293698 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:17147489 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003800 monodactyly IAGP N RGD:5509061 20141003 MGI PMID:15537447 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12509515 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19837032 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:11956231 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:15537447 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:16293698 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:17147489 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:19041748 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:21602802 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:23945236 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20210930 MGI PMID:33905568 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20170706 MGI PMID:28356706 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23945236 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004149 increased bone strength IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:17147489 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12509515 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:16293698 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:11956231 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:16293698 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:19041748 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:17147489 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:11956231 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:16293698 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15537447 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12509515 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005201 abnormal retina pigment epithelium morphology IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12509515 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:19041748 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12509515 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005430 absent fibula IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20230511 MGI PMID:33497368 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:19041748 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:21602802 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:23945236 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11956231 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20170706 MGI PMID:28356706 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0006303 abnormal retina nerve fiber layer morphology IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0008067 retina ganglion cell degeneration IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:12509515 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0008156 decreased diameter of tibia IAGP N RGD:5509061 20141003 MGI PMID:12509515 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11956231 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0008274 failure of bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0008450 retina photoreceptor degeneration IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0008512 disorganized retina inner nuclear layer IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0008513 thin retina inner plexiform layer IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0008515 thin retina outer nuclear layer IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0008516 disorganized retina outer nuclear layer IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0008519 thin retina outer plexiform layer IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0008520 disorganized retina outer plexiform layer IEA N RGD:5509061 20111116 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23945236 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20230511 MGI PMID:33497368 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0009869 abnormal descending aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:19837032 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180927 MGI PMID:19041748 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180927 MGI PMID:19041748 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20161117 MGI PMID:27524797 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20170706 MGI PMID:28356706 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:23945236 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23945236 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:17147489 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:23945236 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:11956231 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010961 increased compact bone mass IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010962 decreased compact bone mass IAGP N RGD:5509061 20141003 MGI PMID:17147489 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0010962 decreased compact bone mass IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11956231 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21924256 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19837032 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20161117 MGI PMID:27524797 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0012035 abnormal b-wave shape IAGP N RGD:5509061 20161117 MGI PMID:27524797 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0012139 increased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20170706 MGI PMID:28356706 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20170706 MGI PMID:28356706 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0013207 absent endoderm IAGP N RGD:5509061 20141003 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0013618 decreased areal bone mineral density IAGP N RGD:5509061 20170706 MGI PMID:28356706 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0013639 decreased bone stiffness IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0013640 increased bone stiffness IAGP N RGD:5509061 20150507 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0013925 abnormal vascular plexus formation IAGP N RGD:5509061 20161117 MGI PMID:27524797 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0014179 abnormal blood-retina barrier function IAGP N RGD:5509061 20170706 MGI PMID:28356706 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:15142971 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:15537447 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:17147489 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:19041748 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:16293698 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:17147489 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:19041748 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:16293698 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:24225945 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0021107 retina fold IEA N RGD:5509061 20220331 MGI 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0030281 thin parietal bone IAGP N RGD:5509061 20171102 MGI PMID:12509515 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0030439 decreased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:19041748 1319618 Lrp5 low density lipoprotein receptor-related protein 5 gene MP:0031606 increased susceptibility to age-related retinal degeneration IEA N RGD:5509061 20240404 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210128 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20231207 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0001261 obese IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0001265 decreased body size IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20210128 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0001406 abnormal gait IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210826 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20190502 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0001525 impaired balance IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151112 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0002652 thin myocardium IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0002833 increased heart weight IEA N RGD:5509061 20200402 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0003717 pallor IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0003900 shortened QT interval IEA N RGD:5509061 20211021 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210520 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0006241 abnormal placement of pupils IEA N RGD:5509061 20210128 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0010571 shortened ST segment IEA N RGD:5509061 20211021 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0011392 increased fetal cardiomyocyte apoptosis IAGP N RGD:5509061 20150924 MGI PMID:24425002 1319621 Ppp2r5c protein phosphatase 2, regulatory subunit B', gamma gene MP:0031611 decreased fetal cardiomyocyte number IAGP N RGD:5509061 20240404 MGI PMID:24425002 1319623 Mmp21 matrix metallopeptidase 21 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20150402 MGI 1319623 Mmp21 matrix metallopeptidase 21 gene MP:0000531 right pulmonary isomerism IEA N RGD:5509061 20150402 MGI 1319623 Mmp21 matrix metallopeptidase 21 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20150402 MGI 1319623 Mmp21 matrix metallopeptidase 21 gene MP:0002639 micrognathia IEA N RGD:5509061 20150402 MGI 1319623 Mmp21 matrix metallopeptidase 21 gene MP:0004110 transposition of great arteries IEA N RGD:5509061 20150402 MGI 1319623 Mmp21 matrix metallopeptidase 21 gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 1319623 Mmp21 matrix metallopeptidase 21 gene MP:0006123 tricuspid valve atresia IEA N RGD:5509061 20141003 MGI 1319623 Mmp21 matrix metallopeptidase 21 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141003 MGI 1319623 Mmp21 matrix metallopeptidase 21 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20150402 MGI 1319623 Mmp21 matrix metallopeptidase 21 gene MP:0010422 heart right ventricle hypoplasia IEA N RGD:5509061 20150402 MGI 1319623 Mmp21 matrix metallopeptidase 21 gene MP:0010808 right-sided stomach IEA N RGD:5509061 20150402 MGI 1319623 Mmp21 matrix metallopeptidase 21 gene MP:0011665 d-loop transposition of the great arteries IEA N RGD:5509061 20141003 MGI 1319623 Mmp21 matrix metallopeptidase 21 gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20150402 MGI 1319623 Mmp21 matrix metallopeptidase 21 gene MP:0011668 double outlet right ventricle, Taussig bing type IEA N RGD:5509061 20150402 MGI 1319627 Ate1 arginyltransferase 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1319627 Ate1 arginyltransferase 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1319627 Ate1 arginyltransferase 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18948421 1319627 Ate1 arginyltransferase 1 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:12098698 1319627 Ate1 arginyltransferase 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0001443 poor grooming IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12098698 1319627 Ate1 arginyltransferase 1 gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12098698 1319627 Ate1 arginyltransferase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18948421 1319627 Ate1 arginyltransferase 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:12098698 1319627 Ate1 arginyltransferase 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12098698 1319627 Ate1 arginyltransferase 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18948421 1319627 Ate1 arginyltransferase 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:19890395 1319627 Ate1 arginyltransferase 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19890395 1319627 Ate1 arginyltransferase 1 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20230601 MGI 1319627 Ate1 arginyltransferase 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1319627 Ate1 arginyltransferase 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:12098698 1319627 Ate1 arginyltransferase 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:18948421 1319627 Ate1 arginyltransferase 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:12098698 1319627 Ate1 arginyltransferase 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:12098698 1319627 Ate1 arginyltransferase 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:18948421 1319627 Ate1 arginyltransferase 1 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:18948421 1319627 Ate1 arginyltransferase 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18948421 1319627 Ate1 arginyltransferase 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:18948421 1319627 Ate1 arginyltransferase 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12098698 1319627 Ate1 arginyltransferase 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:12098698 1319627 Ate1 arginyltransferase 1 gene MP:0010502 ventricle myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12098698 1319627 Ate1 arginyltransferase 1 gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12098698 1319627 Ate1 arginyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1319627 Ate1 arginyltransferase 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18948421 1319627 Ate1 arginyltransferase 1 gene MP:0011854 cerebral edema IAGP N RGD:5509061 20141003 MGI PMID:19915679 1319627 Ate1 arginyltransferase 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20240523 MGI 1319627 Ate1 arginyltransferase 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:19915679 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:21768366 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:21768366 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21768366 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16287858 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17855341 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:16287858 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:23102580 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:21768366 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0003436 decreased susceptibility to induced arthritis IEA N RGD:5509061 20111116 MGI 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21768366 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21768366 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IEA N RGD:5509061 20111116 MGI 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0005095 decreased T cell proliferation IEA N RGD:5509061 20111116 MGI 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0008088 abnormal T-helper 1 cell differentiation IEA N RGD:5509061 20111116 MGI 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0008092 abnormal T-helper 2 cell differentiation IEA N RGD:5509061 20111116 MGI 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0008561 decreased tumor necrosis factor secretion IEA N RGD:5509061 20111116 MGI 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0008567 decreased interferon-gamma secretion IEA N RGD:5509061 20111116 MGI 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0008660 increased interleukin-10 secretion IEA N RGD:5509061 20111116 MGI 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20150702 MGI PMID:16287858 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:21768366 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0010221 abnormal T-helper 17 cell differentiation IEA N RGD:5509061 20111116 MGI 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:21768366 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21768366 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21768366 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0011394 increased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20240118 MGI PMID:21768366 1319635 Mapk11 mitogen-activated protein kinase 11 gene MP:0031526 thin right ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:21768366 1319636 Tmem192 transmembrane protein 192 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:28504966 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11688556 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15548583 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15548583 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:11688556 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15548583 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:11688556 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:11688556 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15548583 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0004181 abnormal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15548583 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:15548583 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0006049 semilunar valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:15548583 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0009389 abnormal extracutaneous pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15548583 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11688556 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0010589 common truncal valve IAGP N RGD:5509061 20141003 MGI PMID:11688556 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11688556 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11688556 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15548583 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20240118 MGI PMID:11688556 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11688556 1319639 Sema3c sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C gene MP:0031517 interrupted aortic arch, type c IAGP N RGD:5509061 20240118 MGI PMID:11688556 1319641 Ropn1l ropporin 1-like gene MP:0000160 kyphosis IEA N RGD:5509061 20160421 MGI 1319641 Ropn1l ropporin 1-like gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201231 MGI 1319641 Ropn1l ropporin 1-like gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22021175 1319641 Ropn1l ropporin 1-like gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20201231 MGI 1319641 Ropn1l ropporin 1-like gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20160421 MGI 1319641 Ropn1l ropporin 1-like gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1319641 Ropn1l ropporin 1-like gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:22021175 1319641 Ropn1l ropporin 1-like gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220714 MGI PMID:22021175 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10533607 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17526724 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:15894265 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:10533607 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17526724 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:21636294 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10533607 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10533607 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23455674 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11092811 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17526724 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17526724 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:23027924 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23455674 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23980208 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:10533607 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:10533607 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11092811 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10533607 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23980208 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:15894265 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:23455674 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:23455674 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:23455674 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:17526724 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002440 abnormal memory B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23027924 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23455674 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11092811 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:23455674 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:10533607 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:22962683 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:23027924 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21636294 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10533607 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:10533607 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21636294 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:23027924 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:23980208 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008179 absent germinal center B cells IAGP N RGD:5509061 20141003 MGI PMID:23027924 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21636294 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23455674 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008194 abnormal memory B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23027924 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:23455674 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:23455674 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:23455674 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008523 absent lymph node germinal center IAGP N RGD:5509061 20141003 MGI PMID:9171827 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:23980208 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:23980208 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:17526724 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220623 MGI PMID:11092811 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0010187 decreased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:21636294 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0010187 decreased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:23027924 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0010187 decreased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:23455674 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0010187 decreased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:23980208 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0010188 abnormal T follicular helper cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23980208 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0010674 increased activation-induced B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21636294 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10533607 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17526724 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23455674 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:11092811 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0020583 decreased ceramide level IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0020867 increased lipogenesis IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20190509 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0030973 impaired gluconeogenesis IAGP N RGD:5509061 20200102 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240321 MGI PMID:30566857 1319643 Bcl6 B cell leukemia/lymphoma 6 gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:30566857 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24185898 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0000608 dissociated hepatocytes IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20200116 MGI PMID:26075877 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20210325 MGI PMID:33296658 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20210128 MGI 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20210325 MGI PMID:33296658 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20210325 MGI PMID:33296658 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20220519 MGI 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210128 MGI 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20200116 MGI PMID:26075877 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0003904 decreased cell mass IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200116 MGI PMID:26075877 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200116 MGI PMID:26075877 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20200116 MGI PMID:26075877 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20200116 MGI PMID:26075877 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20200116 MGI PMID:26075877 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20200116 MGI PMID:26075877 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:26075877 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:26075877 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20200116 MGI PMID:26075877 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20200116 MGI PMID:26075877 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20210325 MGI PMID:33296658 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0010889 small alveolar lamellar bodies IAGP N RGD:5509061 20210325 MGI PMID:33296658 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0010890 decreased alveolar lamellar body number IAGP N RGD:5509061 20210325 MGI PMID:33296658 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20210325 MGI PMID:33296658 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20716775 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:26075877 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17015619 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200116 MGI PMID:26075877 1319645 Rb1cc1 RB1-inducible coiled-coil 1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:26075877 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16537918 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19364276 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201022 MGI 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20201022 MGI 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16537918 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0001095 enlarged trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:15492043 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19364276 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:16537918 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201022 MGI 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17159989 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17159989 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:17159989 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17159989 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:17159989 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:19364276 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:19364276 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20201022 MGI 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16537918 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:19364276 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:17159989 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17159989 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20141003 MGI PMID:17159989 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20160421 MGI 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16537918 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:17159989 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:17159989 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16537918 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0006102 decreased tegmentum size IAGP N RGD:5509061 20141003 MGI PMID:17159989 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:16537918 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:16537918 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:19364276 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:17159989 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16537918 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:17159989 1319650 Hipk2 homeodomain interacting protein kinase 2 gene MP:0020543 decreased substantia nigra size IAGP N RGD:5509061 20180301 MGI PMID:17159989 1319651 Urah urate (5-hydroxyiso-) hydrolase gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:20823251 1319651 Urah urate (5-hydroxyiso-) hydrolase gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20823251 1319651 Urah urate (5-hydroxyiso-) hydrolase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20823251 1319651 Urah urate (5-hydroxyiso-) hydrolase gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20823251 1319651 Urah urate (5-hydroxyiso-) hydrolase gene MP:0005068 abnormal NK cell morphology IAGP N RGD:5509061 20220428 MGI PMID:30383838 1319651 Urah urate (5-hydroxyiso-) hydrolase gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20220428 MGI PMID:30383838 1319651 Urah urate (5-hydroxyiso-) hydrolase gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:20823251 1319651 Urah urate (5-hydroxyiso-) hydrolase gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20220428 MGI PMID:30383838 1319651 Urah urate (5-hydroxyiso-) hydrolase gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20823251 1319651 Urah urate (5-hydroxyiso-) hydrolase gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20220428 MGI PMID:30383838 1319651 Urah urate (5-hydroxyiso-) hydrolase gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20220428 MGI PMID:30383838 1319653 Fes feline sarcoma oncogene gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11021537 1319653 Fes feline sarcoma oncogene gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11021537 1319653 Fes feline sarcoma oncogene gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11021537 1319653 Fes feline sarcoma oncogene gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:11021537 1319653 Fes feline sarcoma oncogene gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:11021537 1319653 Fes feline sarcoma oncogene gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0000798 abnormal frontal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:11021537 1319653 Fes feline sarcoma oncogene gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11909942 1319653 Fes feline sarcoma oncogene gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11021537 1319653 Fes feline sarcoma oncogene gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11021537 1319653 Fes feline sarcoma oncogene gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:11021537 1319653 Fes feline sarcoma oncogene gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0001934 increased litter size IAGP N RGD:5509061 20141003 MGI PMID:11909942 1319653 Fes feline sarcoma oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10523632 1319653 Fes feline sarcoma oncogene gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:11021537 1319653 Fes feline sarcoma oncogene gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11021537 1319653 Fes feline sarcoma oncogene gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11021537 1319653 Fes feline sarcoma oncogene gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11021537 1319653 Fes feline sarcoma oncogene gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11909942 1319653 Fes feline sarcoma oncogene gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11909942 1319653 Fes feline sarcoma oncogene gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11909942 1319653 Fes feline sarcoma oncogene gene MP:0003749 down-turned corners of mouth IAGP N RGD:5509061 20171019 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11021537 1319653 Fes feline sarcoma oncogene gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11909942 1319653 Fes feline sarcoma oncogene gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:11909942 1319653 Fes feline sarcoma oncogene gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11909942 1319653 Fes feline sarcoma oncogene gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:11909942 1319653 Fes feline sarcoma oncogene gene MP:0009432 increased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:15867340 1319653 Fes feline sarcoma oncogene gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11977979 1319653 Fes feline sarcoma oncogene gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11021537 1319653 Fes feline sarcoma oncogene gene MP:0030192 downturned snout IAGP N RGD:5509061 20171019 MGI PMID:11977979 1319656 Mrc1 mannose receptor, C type 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:23319563 1319656 Mrc1 mannose receptor, C type 1 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:11805139 1319656 Mrc1 mannose receptor, C type 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:11805139 1319656 Mrc1 mannose receptor, C type 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11805139 1319656 Mrc1 mannose receptor, C type 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17596337 1319656 Mrc1 mannose receptor, C type 1 gene MP:0003369 abnormal circulating estrogen level IAGP N RGD:5509061 20141003 MGI PMID:11805139 1319656 Mrc1 mannose receptor, C type 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23319563 1319656 Mrc1 mannose receptor, C type 1 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:23319563 1319656 Mrc1 mannose receptor, C type 1 gene MP:0010751 decreased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23319563 1319656 Mrc1 mannose receptor, C type 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11805139 1319658 Ctsw cathepsin W gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15087452 1319661 Rxylt1 ribitol xylosyltransferase 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20210128 MGI 1319661 Rxylt1 ribitol xylosyltransferase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1319661 Rxylt1 ribitol xylosyltransferase 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20210128 MGI 1319661 Rxylt1 ribitol xylosyltransferase 1 gene MP:0001523 impaired righting response IEA N RGD:5509061 20210128 MGI 1319661 Rxylt1 ribitol xylosyltransferase 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 1319661 Rxylt1 ribitol xylosyltransferase 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1319661 Rxylt1 ribitol xylosyltransferase 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1319661 Rxylt1 ribitol xylosyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319663 Lrfn5 leucine rich repeat and fibronectin type III domain containing 5 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 1319663 Lrfn5 leucine rich repeat and fibronectin type III domain containing 5 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20240523 MGI 1319663 Lrfn5 leucine rich repeat and fibronectin type III domain containing 5 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 1319663 Lrfn5 leucine rich repeat and fibronectin type III domain containing 5 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20240523 MGI 1319666 Unc119b unc-119 lipid binding chaperone B gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 1319666 Unc119b unc-119 lipid binding chaperone B gene MP:0005586 decreased tidal volume IEA N RGD:5509061 20211021 MGI 1319667 Rgs7bp regulator of G-protein signalling 7 binding protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18842904 1319669 Col8a1 collagen, type VIII, alpha 1 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:16051690 1319669 Col8a1 collagen, type VIII, alpha 1 gene MP:0004284 abnormal Descemet membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16051690 1319669 Col8a1 collagen, type VIII, alpha 1 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16051690 1319669 Col8a1 collagen, type VIII, alpha 1 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:16051690 1319669 Col8a1 collagen, type VIII, alpha 1 gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16051690 1319669 Col8a1 collagen, type VIII, alpha 1 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:16051690 1319669 Col8a1 collagen, type VIII, alpha 1 gene MP:0031177 decreased Descemet membrane thickness IAGP N RGD:5509061 20201119 MGI PMID:16051690 1319669 Col8a1 collagen, type VIII, alpha 1 gene MP:0031213 increased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:16051690 1319672 Cdca7 cell division cycle associated 7 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20240404 MGI PMID:38335290 1319674 F11 coagulation factor XI gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0002343 abnormal lymph node cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:16533887 1319674 F11 coagulation factor XI gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:16533887 1319674 F11 coagulation factor XI gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20151203 MGI PMID:16009717 1319674 F11 coagulation factor XI gene MP:0010178 increased number of Howell-Jolly bodies IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0012359 increased partial thromboplastin time IAGP N RGD:5509061 20141003 MGI PMID:9518045 1319674 F11 coagulation factor XI gene MP:0031051 lymph node hemorrhage IAGP N RGD:5509061 20200618 MGI PMID:11159184 1319674 F11 coagulation factor XI gene MP:0031126 gangrene IAGP N RGD:5509061 20200917 MGI PMID:11159184 1319682 Med30 mediator complex subunit 30 gene MP:0000278 abnormal myocardial fiber morphology IEA N RGD:5509061 20141003 MGI 1319682 Med30 mediator complex subunit 30 gene MP:0001577 anemia IEA N RGD:5509061 20141003 MGI 1319682 Med30 mediator complex subunit 30 gene MP:0001634 internal hemorrhage IEA N RGD:5509061 20141003 MGI 1319682 Med30 mediator complex subunit 30 gene MP:0002083 premature death IEA N RGD:5509061 20141003 MGI 1319682 Med30 mediator complex subunit 30 gene MP:0003135 increased erythroid progenitor cell number IEA N RGD:5509061 20141003 MGI 1319682 Med30 mediator complex subunit 30 gene MP:0003141 cardiac fibrosis IEA N RGD:5509061 20141003 MGI 1319682 Med30 mediator complex subunit 30 gene MP:0004090 abnormal sarcomere morphology IEA N RGD:5509061 20141003 MGI 1319682 Med30 mediator complex subunit 30 gene MP:0004091 abnormal Z line morphology IEA N RGD:5509061 20141003 MGI 1319682 Med30 mediator complex subunit 30 gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20141003 MGI 1319682 Med30 mediator complex subunit 30 gene MP:0005150 cachexia IEA N RGD:5509061 20141003 MGI 1319682 Med30 mediator complex subunit 30 gene MP:0005330 cardiomyopathy IEA N RGD:5509061 20141003 MGI 1319682 Med30 mediator complex subunit 30 gene MP:0006035 abnormal mitochondrial morphology IEA N RGD:5509061 20141003 MGI 1319682 Med30 mediator complex subunit 30 gene MP:0006036 abnormal mitochondrial physiology IEA N RGD:5509061 20141003 MGI 1319682 Med30 mediator complex subunit 30 gene MP:0006085 myocardium necrosis IEA N RGD:5509061 20141003 MGI 1319682 Med30 mediator complex subunit 30 gene MP:0006138 congestive heart failure IEA N RGD:5509061 20141003 MGI 1319682 Med30 mediator complex subunit 30 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22106289 1319682 Med30 mediator complex subunit 30 gene MP:0030567 abnormal I band morphology IEA N RGD:5509061 20180531 MGI 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20170302 MGI PMID:27013658 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20170601 MGI PMID:26774178 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20170302 MGI PMID:27013658 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20170601 MGI PMID:26774178 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20170302 MGI PMID:27013658 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170302 MGI PMID:27013658 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170601 MGI PMID:26774178 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20170302 MGI PMID:27013658 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20170302 MGI PMID:27013658 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20170302 MGI PMID:27013658 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20170302 MGI PMID:27013658 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20170302 MGI PMID:27013658 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20170601 MGI PMID:26774178 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20170302 MGI PMID:27013658 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20170601 MGI PMID:26774178 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20170302 MGI PMID:27013658 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20170302 MGI PMID:27013658 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20170302 MGI PMID:27013658 1319684 Tm6sf2 transmembrane 6 superfamily member 2 gene MP:0010332 abnormal circulating apolipoprotein level IAGP N RGD:5509061 20170302 MGI PMID:27013658 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0000692 small spleen IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12818157 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001147 small testis IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:12818157 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:12818157 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12867037 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12818157 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12867037 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12867038 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12867037 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12867038 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:12818157 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:12867038 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:16751370 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:22075698 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12818157 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:16751370 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12818157 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12867038 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:16751370 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:22075698 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12867038 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12867037 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12818157 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12867038 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12818157 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16751370 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12818157 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0003454 erythroderma IAGP N RGD:5509061 20141003 MGI PMID:12818157 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12818157 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0005015 increased T cell number IEA N RGD:5509061 20190530 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20190530 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0005078 abnormal cytotoxic T cell physiology IEA N RGD:5509061 20111116 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12867037 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12867038 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12867037 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12867038 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008039 increased NK T cell number IEA N RGD:5509061 20190606 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16751370 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16751370 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16751370 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12818157 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008169 increased B-1b cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008176 abnormal germinal center B cell morphology IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008203 absent B-1a cells IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008203 absent B-1a cells IAGP N RGD:5509061 20141003 MGI PMID:12867038 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008213 absent immature B cells IAGP N RGD:5509061 20141003 MGI PMID:12867037 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008397 abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12867037 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12867038 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12867037 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:12867037 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:12867038 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:12818157 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:12867037 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:12867038 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008567 decreased interferon-gamma secretion IEA N RGD:5509061 20111116 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:16751370 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008627 decreased circulating interleukin-5 level IAGP N RGD:5509061 20141003 MGI PMID:16751370 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008686 abnormal interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:12818158 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008688 decreased interleukin-2 secretion IEA N RGD:5509061 20111116 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20141003 MGI PMID:19260764 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0009709 hydrometra IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0009925 increased transitional stage T2 B cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0010228 decreased transitional stage T3 B cell number IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0010766 abnormal NK cell physiology IEA N RGD:5509061 20111116 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0010842 decreased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190530 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0010845 decreased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190530 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0010851 decreased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190530 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20190404 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0013436 increased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0013763 increased T-helper cell number IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0013771 decreased effector memory T-helper cell number IEA N RGD:5509061 20230119 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20190606 MGI 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0020154 impaired humoral immune response IAGP N RGD:5509061 20210128 MGI PMID:31784498 1319686 Card11 caspase recruitment domain family, member 11 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230119 MGI 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:10589692 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:10589692 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20201231 MGI 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:10589692 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:10589692 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000829 dilated fourth ventricle IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0000917 obstructive hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10589692 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:10589692 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10589692 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10589692 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10589692 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10589692 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:10589692 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18387364 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0003657 abnormal erythrocyte osmotic lysis IAGP N RGD:5509061 20141003 MGI PMID:10589692 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:10589692 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20190502 MGI 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20200402 MGI 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:10589692 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:10589692 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20190502 MGI 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9070925 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0011952 decreased cardiac stroke volume IEA N RGD:5509061 20220519 MGI 1319691 Nek1 NIMA (never in mitosis gene a)-related expressed kinase 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1319693 Rec8 REC8 meiotic recombination protein gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15935783 1319693 Rec8 REC8 meiotic recombination protein gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:15935783 1319693 Rec8 REC8 meiotic recombination protein gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:15515002 1319693 Rec8 REC8 meiotic recombination protein gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15515002 1319693 Rec8 REC8 meiotic recombination protein gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1319693 Rec8 REC8 meiotic recombination protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15935783 1319693 Rec8 REC8 meiotic recombination protein gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:15515002 1319693 Rec8 REC8 meiotic recombination protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15935783 1319693 Rec8 REC8 meiotic recombination protein gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15935783 1319693 Rec8 REC8 meiotic recombination protein gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:15935783 1319693 Rec8 REC8 meiotic recombination protein gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20150226 MGI PMID:24589552 1319693 Rec8 REC8 meiotic recombination protein gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15935783 1319693 Rec8 REC8 meiotic recombination protein gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:15515002 1319693 Rec8 REC8 meiotic recombination protein gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:15935783 1319693 Rec8 REC8 meiotic recombination protein gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:15935783 1319693 Rec8 REC8 meiotic recombination protein gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:15935783 1319693 Rec8 REC8 meiotic recombination protein gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:15935783 1319693 Rec8 REC8 meiotic recombination protein gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:15935783 1319693 Rec8 REC8 meiotic recombination protein gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:20971813 1319693 Rec8 REC8 meiotic recombination protein gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:15515002 1319693 Rec8 REC8 meiotic recombination protein gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:24413433 1319693 Rec8 REC8 meiotic recombination protein gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20150226 MGI PMID:24589552 1319693 Rec8 REC8 meiotic recombination protein gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20210304 MGI PMID:30853435 1319693 Rec8 REC8 meiotic recombination protein gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1319693 Rec8 REC8 meiotic recombination protein gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1319693 Rec8 REC8 meiotic recombination protein gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1319693 Rec8 REC8 meiotic recombination protein gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:15515002 1319693 Rec8 REC8 meiotic recombination protein gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:15935783 1319693 Rec8 REC8 meiotic recombination protein gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20150226 MGI PMID:24589552 1319693 Rec8 REC8 meiotic recombination protein gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20150226 MGI PMID:24589552 1319693 Rec8 REC8 meiotic recombination protein gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20150226 MGI PMID:24589552 1319693 Rec8 REC8 meiotic recombination protein gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20210304 MGI PMID:30853435 1319693 Rec8 REC8 meiotic recombination protein gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1319693 Rec8 REC8 meiotic recombination protein gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20210304 MGI PMID:30853435 1319693 Rec8 REC8 meiotic recombination protein gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15935783 1319695 Scap SREBF chaperone gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1319695 Scap SREBF chaperone gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11358865 1319695 Scap SREBF chaperone gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:11358865 1319695 Scap SREBF chaperone gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11358865 1319695 Scap SREBF chaperone gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11358865 1319695 Scap SREBF chaperone gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11358865 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20200402 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19060883 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19060883 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23785118 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23785118 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19060883 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20201022 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20210128 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20210520 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20201022 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200402 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20201022 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:19060883 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19060883 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20210128 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:19060883 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20181011 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200402 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20210128 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20200402 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0005425 increased macrophage cell number IEA N RGD:5509061 20181011 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23785118 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008126 increased dendritic cell number IEA N RGD:5509061 20181011 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008167 increased B-1a cell number IEA N RGD:5509061 20181011 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20181011 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20181011 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23785118 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008524 increased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23785118 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20181011 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23785118 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:23785118 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008690 increased interleukin-23 secretion IAGP N RGD:5509061 20141003 MGI PMID:23785118 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:23785118 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:19060883 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20200402 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20230601 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23785118 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19060883 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22011580 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20210128 MGI 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:19060883 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:21606507 1319698 Tnip1 TNFAIP3 interacting protein 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:18725525 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:21098571 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20181227 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15613470 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17613256 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170824 MGI PMID:18256189 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170824 MGI PMID:18256189 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231123 MGI PMID:20018673 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18591425 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18591425 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:23974039 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16462742 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:22474261 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000380 small hair follicles IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:16682203 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:18591425 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:16682203 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:21098571 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:16040801 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:16040801 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:15613470 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000690 absent spleen IEA N RGD:5509061 20200402 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18725525 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18725527 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18725525 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18725527 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:22179202 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:21098571 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:21098571 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:15867090 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21098571 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20200116 MGI PMID:18463241 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21098571 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19129368 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001147 small testis IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:16452165 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16682203 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18591425 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:16682203 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001219 thick epidermis IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18725525 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23974039 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160204 MGI PMID:22331912 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160204 MGI PMID:25815421 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001280 loss of vibrissae IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20200116 MGI PMID:18463241 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001341 absent eyelids IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20170824 MGI PMID:18256189 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:16462742 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17397913 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15613470 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:23918385 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14528307 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15613470 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18591425 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:15613470 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:14528307 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16040801 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16682203 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001762 polyuria IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:17397913 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:22117047 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18329371 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:22179202 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20170824 MGI PMID:18256189 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18725525 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18725527 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18725525 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18725527 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001863 blood vessel inflammation IAGP N RGD:5509061 20141003 MGI PMID:18725527 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22701646 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001925 male infertility IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19129368 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:24209619 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:22331912 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:25815421 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16682203 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18725525 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18725527 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002083 premature death IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002083 premature death IAGP N RGD:5509061 20160204 MGI PMID:22331912 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002083 premature death IAGP N RGD:5509061 20160204 MGI PMID:25815421 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:16462742 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22117047 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18591425 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160218 MGI PMID:25329700 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20170824 MGI PMID:18256189 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22179202 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:22179202 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18725525 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:22117047 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:22701646 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:21098571 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002639 micrognathia IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22701646 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002750 exophthalmos IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20170824 MGI PMID:18256189 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170824 MGI PMID:18256189 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002827 abnormal renal corpuscle morphology IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002871 albuminuria IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003054 spina bifida IAGP N RGD:5509061 20180531 MGI PMID:28337978 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20170824 MGI PMID:18256189 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20181129 MGI PMID:16682203 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:22474261 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16040801 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20141003 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20160204 MGI PMID:22331912 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:22331912 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:25815421 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003670 dilated renal glomerular capsule IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003700 abnormal oviduct transport IAGP N RGD:5509061 20141003 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:16682203 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:22474261 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:23974039 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16040801 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:22179202 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20200116 MGI PMID:18463241 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:22179202 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:16682203 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003875 abnormal hair follicle regression IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:20360310 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:18591425 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15613470 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20170824 MGI PMID:18256189 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004458 absent alisphenoid bone IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004592 small mandible IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004728 abnormal efferent ductules of testis morphology IAGP N RGD:5509061 20141003 MGI PMID:22701646 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004880 lung cyst IAGP N RGD:5509061 20160324 MGI PMID:25978641 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004882 enlarged lung IAGP N RGD:5509061 20160324 MGI PMID:25978641 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004899 absent temporal bone squamous part IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:22179202 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:18725525 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:22701646 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22701646 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004941 abnormal regulatory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18725525 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18725525 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004969 pale kidney IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18725525 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18725527 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20181011 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18329371 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:15867090 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16009718 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16009718 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16009718 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005150 cachexia IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:19129368 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:24209619 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005324 ascites IAGP N RGD:5509061 20160204 MGI PMID:22331912 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005324 ascites IAGP N RGD:5509061 20160204 MGI PMID:25815421 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17397913 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20170824 MGI PMID:18256189 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18725525 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:16009718 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:16009718 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:22474261 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:18256189 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16009718 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18591425 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16462742 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231123 MGI PMID:20018673 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20170824 MGI PMID:18256189 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006213 shallow orbits IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:18591425 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:21098571 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16452165 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20160324 MGI PMID:25978641 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16009718 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0006428 ectopic Sertoli cells IAGP N RGD:5509061 20141003 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:18591425 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008018 increased facial tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22179202 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22179202 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008083 decreased single-positive T cell number IEA N RGD:5509061 20181011 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008094 absent memory B cells IAGP N RGD:5509061 20141003 MGI PMID:22117047 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:22117047 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008100 absent plasma cells IAGP N RGD:5509061 20141003 MGI PMID:22117047 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:22117047 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18329371 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22117047 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18329371 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18329371 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18329371 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008257 thin myometrium IAGP N RGD:5509061 20141003 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15867090 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200116 MGI PMID:18463241 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:18463241 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008755 abnormal immunoglobulin V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:18329371 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18725525 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18725525 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009071 short oviduct IAGP N RGD:5509061 20141003 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009089 short uterine horn IAGP N RGD:5509061 20141003 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009096 decreased endometrial gland number IAGP N RGD:5509061 20141003 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009140 dilated efferent ductule of testis IAGP N RGD:5509061 20141003 MGI PMID:22701646 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009235 small sperm head IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009236 pinhead sperm IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009242 thin sperm flagellum IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009392 retina gliosis IAGP N RGD:5509061 20200116 MGI PMID:18463241 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009439 increased myeloid sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22179202 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009600 hypergranulosis IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009759 abnormal hair follicle bulge morphology IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:19129368 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:23974039 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0010241 abnormal aortic arch development IAGP N RGD:5509061 20141003 MGI PMID:21098571 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20150326 MGI PMID:24979267 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:21098571 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231123 MGI PMID:20018673 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20231123 MGI PMID:20018673 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:22434867 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0010964 increased compact bone volume IAGP N RGD:5509061 20141003 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0010976 small lung lobe IAGP N RGD:5509061 20141003 MGI PMID:16452165 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20160324 MGI PMID:25978641 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16462742 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170824 MGI PMID:18256189 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16682203 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16452165 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180531 MGI PMID:28337978 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16575173 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17613256 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23918385 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14528307 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16040801 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17397913 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20231123 MGI PMID:20018673 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15613470 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21098571 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16575173 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011142 abnormal lung-associated mesenchyme development IAGP N RGD:5509061 20160324 MGI PMID:25978641 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011147 increased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20160324 MGI PMID:25978641 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22701646 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011846 decreased kidney collecting duct number IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20170824 MGI PMID:18256189 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:18463241 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:18463241 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20180531 MGI PMID:28337978 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20200827 MGI PMID:31766249 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0013305 isosthenuria IAGP N RGD:5509061 20160929 MGI PMID:25799508 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0013600 testis degeneration IAGP N RGD:5509061 20150312 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0014194 increased epididymal epithelium cell proliferation IAGP N RGD:5509061 20160526 MGI PMID:22701646 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:16040801 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0014445 abnormal spindle assembly in female meiosis IAGP N RGD:5509061 20240509 MGI PMID:19129368 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0014445 abnormal spindle assembly in female meiosis IAGP N RGD:5509061 20240509 MGI PMID:24209619 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:17613256 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:17613256 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:17613256 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0021086 decreased DNA replication IAGP N RGD:5509061 20220310 MGI PMID:18591425 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0021217 abnormal palatal shelf bone ossification IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0030025 giant platelets IAGP N RGD:5509061 20170803 MGI PMID:20305640 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0030102 absent orbitosphenoid bone IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0030262 frontal bossing IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0030266 small vomer bone IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0030301 abnormal maxillary frontal process morphology IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0030315 small neurocranium IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0030575 decreased hair follicle cell proliferation IAGP N RGD:5509061 20181129 MGI PMID:16682203 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0030591 absent sperm fibrous sheath IAGP N RGD:5509061 20220324 MGI PMID:21949761 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0030920 small hair follicle bulb IAGP N RGD:5509061 20181220 MGI PMID:16682203 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0031147 abnormal ventricular thrombosis IAGP N RGD:5509061 20201224 MGI PMID:18256189 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0031407 increased Sertoli cell proliferation IAGP N RGD:5509061 20220630 MGI PMID:19071104 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:18703631 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230316 MGI PMID:23716939 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:18463241 1319700 Dicer1 dicer 1, ribonuclease type III gene MP:0031613 fetal cardiomyocyte disarray IAGP N RGD:5509061 20240321 MGI PMID:18256189 1319704 Rnf24 ring finger protein 24 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 1319704 Rnf24 ring finger protein 24 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1319714 Hmcn2 hemicentin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210429 MGI PMID:32035013 1319714 Hmcn2 hemicentin 2 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20201022 MGI 1319714 Hmcn2 hemicentin 2 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20221215 MGI 1319714 Hmcn2 hemicentin 2 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20201022 MGI 1319716 Cmtr2 cap methyltransferase 2 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20181227 MGI 1319716 Cmtr2 cap methyltransferase 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1319716 Cmtr2 cap methyltransferase 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1319716 Cmtr2 cap methyltransferase 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1319716 Cmtr2 cap methyltransferase 2 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1319716 Cmtr2 cap methyltransferase 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230601 MGI 1319716 Cmtr2 cap methyltransferase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319720 Tbx20 T-box 20 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1319720 Tbx20 T-box 20 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:15901664 1319720 Tbx20 T-box 20 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1319720 Tbx20 T-box 20 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15901664 1319720 Tbx20 T-box 20 gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20210128 MGI 1319720 Tbx20 T-box 20 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15843407 1319720 Tbx20 T-box 20 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15901664 1319720 Tbx20 T-box 20 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:23824573 1319720 Tbx20 T-box 20 gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:23824573 1319720 Tbx20 T-box 20 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:23824573 1319720 Tbx20 T-box 20 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20210826 MGI 1319720 Tbx20 T-box 20 gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20230601 MGI 1319720 Tbx20 T-box 20 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20220519 MGI 1319720 Tbx20 T-box 20 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210826 MGI 1319720 Tbx20 T-box 20 gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20210128 MGI 1319720 Tbx20 T-box 20 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15843407 1319720 Tbx20 T-box 20 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15901664 1319720 Tbx20 T-box 20 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15901664 1319720 Tbx20 T-box 20 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23824573 1319720 Tbx20 T-box 20 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:15901664 1319720 Tbx20 T-box 20 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210128 MGI 1319720 Tbx20 T-box 20 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23824573 1319720 Tbx20 T-box 20 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1319720 Tbx20 T-box 20 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15843407 1319720 Tbx20 T-box 20 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20210128 MGI 1319720 Tbx20 T-box 20 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20210128 MGI 1319720 Tbx20 T-box 20 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20210128 MGI 1319720 Tbx20 T-box 20 gene MP:0003385 abnormal body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20230601 MGI 1319720 Tbx20 T-box 20 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15843407 1319720 Tbx20 T-box 20 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15901664 1319720 Tbx20 T-box 20 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20210128 MGI 1319720 Tbx20 T-box 20 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15901664 1319720 Tbx20 T-box 20 gene MP:0004063 dilated heart left atrium IAGP N RGD:5509061 20231221 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:15843407 1319720 Tbx20 T-box 20 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:15901664 1319720 Tbx20 T-box 20 gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:23824573 1319720 Tbx20 T-box 20 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20201029 MGI PMID:32035085 1319720 Tbx20 T-box 20 gene MP:0009806 abnormal otic vesicle morphology IEA N RGD:5509061 20230601 MGI 1319720 Tbx20 T-box 20 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0010432 common ventricle IAGP N RGD:5509061 20201029 MGI PMID:32035085 1319720 Tbx20 T-box 20 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15843407 1319720 Tbx20 T-box 20 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15901664 1319720 Tbx20 T-box 20 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23824573 1319720 Tbx20 T-box 20 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319720 Tbx20 T-box 20 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1319720 Tbx20 T-box 20 gene MP:0020516 abnormal visceral yolk sac mesenchyme morphology IAGP N RGD:5509061 20180125 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231221 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:15843414 1319720 Tbx20 T-box 20 gene MP:0031572 small atrioventricular valve IAGP N RGD:5509061 20240125 MGI PMID:23824573 1319720 Tbx20 T-box 20 gene MP:0031582 small semilunar valve IAGP N RGD:5509061 20240125 MGI PMID:23824573 1319720 Tbx20 T-box 20 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15843414 1319722 Sucla2 succinate-Coenzyme A ligase, ADP-forming, beta subunit gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141016 MGI PMID:24271779 1319722 Sucla2 succinate-Coenzyme A ligase, ADP-forming, beta subunit gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20180510 MGI PMID:27496549 1319722 Sucla2 succinate-Coenzyme A ligase, ADP-forming, beta subunit gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20180510 MGI PMID:27496549 1319722 Sucla2 succinate-Coenzyme A ligase, ADP-forming, beta subunit gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141016 MGI PMID:24271779 1319722 Sucla2 succinate-Coenzyme A ligase, ADP-forming, beta subunit gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141016 MGI PMID:24271779 1319722 Sucla2 succinate-Coenzyme A ligase, ADP-forming, beta subunit gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141016 MGI PMID:24271779 1319722 Sucla2 succinate-Coenzyme A ligase, ADP-forming, beta subunit gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180510 MGI PMID:27496549 1319722 Sucla2 succinate-Coenzyme A ligase, ADP-forming, beta subunit gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20180510 MGI PMID:27496549 1319722 Sucla2 succinate-Coenzyme A ligase, ADP-forming, beta subunit gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141016 MGI PMID:24271779 1319722 Sucla2 succinate-Coenzyme A ligase, ADP-forming, beta subunit gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20141016 MGI PMID:24271779 1319722 Sucla2 succinate-Coenzyme A ligase, ADP-forming, beta subunit gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20180510 MGI PMID:27496549 1319722 Sucla2 succinate-Coenzyme A ligase, ADP-forming, beta subunit gene MP:0014388 decreased hepatocyte mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:27496549 1319722 Sucla2 succinate-Coenzyme A ligase, ADP-forming, beta subunit gene MP:0014390 decreased myocardial fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:27496549 1319722 Sucla2 succinate-Coenzyme A ligase, ADP-forming, beta subunit gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20190711 MGI PMID:24271779 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19409822 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:23361909 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:23361909 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:7753194 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:7753195 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:7753194 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:7753194 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0000691 enlarged spleen IEA N RGD:5509061 20111116 MGI 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23361909 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7753194 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7753195 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7753194 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19409822 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7753195 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:23361909 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:23361909 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:19409822 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:19409822 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19409822 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23361909 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:7753194 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19409822 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23361909 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:19409822 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7753195 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0004756 abnormal proximal convoluted tubule morphology IEA N RGD:5509061 20111116 MGI 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19409822 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0005096 erythroblastosis IAGP N RGD:5509061 20141003 MGI PMID:7753194 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:19409822 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:23361909 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:19409822 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:23361909 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0008807 increased liver iron level IEA N RGD:5509061 20111116 MGI 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0008809 increased spleen iron level IEA N RGD:5509061 20111116 MGI 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0009395 increased nucleated erythrocyte cell number IEA N RGD:5509061 20111116 MGI 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0010375 increased kidney iron level IEA N RGD:5509061 20111116 MGI 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19409822 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7753194 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7753195 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:23361909 1319724 Klf1 Kruppel-like transcription factor 1 (erythroid) gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:19409822 1319726 Lamc3 laminin gamma 3 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17711601 1319726 Lamc3 laminin gamma 3 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1319726 Lamc3 laminin gamma 3 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17711601 1319726 Lamc3 laminin gamma 3 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:17711601 1319726 Lamc3 laminin gamma 3 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17711601 1319726 Lamc3 laminin gamma 3 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:17711601 1319726 Lamc3 laminin gamma 3 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:17711601 1319726 Lamc3 laminin gamma 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1319727 Ift20 intraflagellar transport 20 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0001925 male infertility IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:18981227 1319727 Ift20 intraflagellar transport 20 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20141003 MGI 1319727 Ift20 intraflagellar transport 20 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:18981227 1319727 Ift20 intraflagellar transport 20 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18981227 1319727 Ift20 intraflagellar transport 20 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18981227 1319727 Ift20 intraflagellar transport 20 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20200123 MGI PMID:21307337 1319727 Ift20 intraflagellar transport 20 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:18981227 1319727 Ift20 intraflagellar transport 20 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:18981227 1319727 Ift20 intraflagellar transport 20 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18981227 1319727 Ift20 intraflagellar transport 20 gene MP:0005571 decreased lactate dehydrogenase level IEA N RGD:5509061 20160804 MGI 1319727 Ift20 intraflagellar transport 20 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20200123 MGI PMID:21307337 1319727 Ift20 intraflagellar transport 20 gene MP:0008448 abnormal retina cone cell inner segment morphology IAGP N RGD:5509061 20200123 MGI PMID:21307337 1319727 Ift20 intraflagellar transport 20 gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20200123 MGI PMID:21307337 1319727 Ift20 intraflagellar transport 20 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20200123 MGI PMID:21307337 1319727 Ift20 intraflagellar transport 20 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18981227 1319727 Ift20 intraflagellar transport 20 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18981227 1319727 Ift20 intraflagellar transport 20 gene MP:0011843 abnormal kidney collecting duct epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18981227 1319727 Ift20 intraflagellar transport 20 gene MP:0020384 absent kidney epithelial cell primary cilium IAGP N RGD:5509061 20161013 MGI PMID:18981227 1319727 Ift20 intraflagellar transport 20 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220224 MGI PMID:27682589 1319727 Ift20 intraflagellar transport 20 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220811 MGI PMID:27682589 1319728 Cend1 cell cycle exit and neuronal differentiation 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20153830 1319728 Cend1 cell cycle exit and neuronal differentiation 1 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:20153830 1319728 Cend1 cell cycle exit and neuronal differentiation 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20153830 1319728 Cend1 cell cycle exit and neuronal differentiation 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20153830 1319728 Cend1 cell cycle exit and neuronal differentiation 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:20153830 1319728 Cend1 cell cycle exit and neuronal differentiation 1 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:20153830 1319728 Cend1 cell cycle exit and neuronal differentiation 1 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20141003 MGI PMID:20153830 1319728 Cend1 cell cycle exit and neuronal differentiation 1 gene MP:0010540 long stride length IAGP N RGD:5509061 20141003 MGI PMID:20153830 1319733 Gpr35 G protein-coupled receptor 35 gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20210211 MGI PMID:32755573 1319733 Gpr35 G protein-coupled receptor 35 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20210211 MGI PMID:32755573 1319733 Gpr35 G protein-coupled receptor 35 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20210916 MGI PMID:33990686 1319733 Gpr35 G protein-coupled receptor 35 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20210916 MGI PMID:33990686 1319733 Gpr35 G protein-coupled receptor 35 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20210916 MGI PMID:33990686 1319733 Gpr35 G protein-coupled receptor 35 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20210211 MGI PMID:32755573 1319733 Gpr35 G protein-coupled receptor 35 gene MP:0013299 decreased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20210916 MGI PMID:33990686 1319733 Gpr35 G protein-coupled receptor 35 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20210211 MGI PMID:32755573 1319735 Fbxo5 F-box protein 5 gene MP:0001304 cataract IEA N RGD:5509061 20230601 MGI 1319735 Fbxo5 F-box protein 5 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:16809773 1319735 Fbxo5 F-box protein 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1319735 Fbxo5 F-box protein 5 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1319735 Fbxo5 F-box protein 5 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1319735 Fbxo5 F-box protein 5 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1319735 Fbxo5 F-box protein 5 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:16809773 1319735 Fbxo5 F-box protein 5 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1319735 Fbxo5 F-box protein 5 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:16809773 1319735 Fbxo5 F-box protein 5 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230601 MGI 1319735 Fbxo5 F-box protein 5 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:16809773 1319735 Fbxo5 F-box protein 5 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16809773 1319735 Fbxo5 F-box protein 5 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:16809773 1319735 Fbxo5 F-box protein 5 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16809773 1319735 Fbxo5 F-box protein 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1319735 Fbxo5 F-box protein 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230601 MGI 1319735 Fbxo5 F-box protein 5 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 1319737 Ndufs3 NADH:ubiquinone oxidoreductase core subunit S3 gene MP:0001391 abnormal tail movements IEA N RGD:5509061 20160804 MGI 1319737 Ndufs3 NADH:ubiquinone oxidoreductase core subunit S3 gene MP:0002833 increased heart weight IEA N RGD:5509061 20141003 MGI 1319737 Ndufs3 NADH:ubiquinone oxidoreductase core subunit S3 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20141003 MGI 1319737 Ndufs3 NADH:ubiquinone oxidoreductase core subunit S3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20141003 MGI 1319737 Ndufs3 NADH:ubiquinone oxidoreductase core subunit S3 gene MP:0005571 decreased lactate dehydrogenase level IEA N RGD:5509061 20160804 MGI 1319739 Ing4 inhibitor of growth family, member 4 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20201022 MGI 1319739 Ing4 inhibitor of growth family, member 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1319739 Ing4 inhibitor of growth family, member 4 gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 1319739 Ing4 inhibitor of growth family, member 4 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1319739 Ing4 inhibitor of growth family, member 4 gene MP:0002989 small kidney IEA N RGD:5509061 20181227 MGI 1319739 Ing4 inhibitor of growth family, member 4 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20210826 MGI 1319739 Ing4 inhibitor of growth family, member 4 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210520 MGI 1319739 Ing4 inhibitor of growth family, member 4 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20240523 MGI 1319739 Ing4 inhibitor of growth family, member 4 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20230601 MGI 1319739 Ing4 inhibitor of growth family, member 4 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20534538 1319739 Ing4 inhibitor of growth family, member 4 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20534538 1319739 Ing4 inhibitor of growth family, member 4 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:20534538 1319739 Ing4 inhibitor of growth family, member 4 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20534538 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20200402 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0000160 kyphosis IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20200402 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0000921 demyelination IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0001257 increased body length IEA N RGD:5509061 20200402 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0001393 ataxia IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0001406 abnormal gait IEA N RGD:5509061 20200402 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0001513 limb grasping IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0002183 gliosis IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20201022 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20200402 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0003439 abnormal glycerol level IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200402 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20200402 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20200402 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200402 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20200402 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0010869 decreased bone trabecula number IEA N RGD:5509061 20211021 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0012220 abnormal ether lipid level IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0013630 increased bone trabecular spacing IEA N RGD:5509061 20211021 MGI 1319744 Acbd5 acyl-Coenzyme A binding domain containing 5 gene MP:0014010 abnormal peroxisome morphology IAGP N RGD:5509061 20210211 MGI PMID:33244184 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20231019 MGI PMID:37553261 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20231019 MGI PMID:37553261 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20231019 MGI PMID:37553261 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0001575 cyanosis IAGP N RGD:5509061 20240425 MGI PMID:37532519 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20231019 MGI PMID:37553261 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20240425 MGI PMID:37532519 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0002188 small heart IAGP N RGD:5509061 20231019 MGI PMID:37553261 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20240425 MGI PMID:37532519 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20231019 MGI PMID:37553261 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20231019 MGI PMID:37553261 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20231019 MGI PMID:37553261 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20240425 MGI PMID:37532519 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231019 MGI PMID:37553261 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20240425 MGI PMID:37532519 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20240425 MGI PMID:37532519 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0010827 small lung saccule IAGP N RGD:5509061 20231019 MGI PMID:37553261 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20231019 MGI PMID:37553261 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20240425 MGI PMID:37532519 1319747 Zswim8 zinc finger SWIM-type containing 8 gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:37553261 1319754 Gpr137 G protein-coupled receptor 137 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1319756 Kctd12 potassium channel tetramerisation domain containing 12 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20160421 MGI PMID:25689571 1319756 Kctd12 potassium channel tetramerisation domain containing 12 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20160421 MGI PMID:25689571 1319756 Kctd12 potassium channel tetramerisation domain containing 12 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20160421 MGI PMID:25689571 1319756 Kctd12 potassium channel tetramerisation domain containing 12 gene MP:0009455 enhanced cued conditioning behavior IAGP N RGD:5509061 20160421 MGI PMID:25689571 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210520 MGI 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0004974 decreased regulatory T cell number IEA N RGD:5509061 20201022 MGI 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20181227 MGI 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0005478 decreased circulating thyroxine level IEA N RGD:5509061 20211021 MGI 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20181227 MGI 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20181227 MGI 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20211021 MGI 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0011338 abnormal mesangial matrix morphology IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0011425 abnormal kidney interstitium morphology IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20181227 MGI 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0012767 increased KLRG1-positive NK cell number IEA N RGD:5509061 20181227 MGI 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319761 Ncf2 neutrophil cytosolic factor 2 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180726 MGI PMID:28471497 1319762 Col9a1 collagen, type IX, alpha 1 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:8197187 1319762 Col9a1 collagen, type IX, alpha 1 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:8197187 1319762 Col9a1 collagen, type IX, alpha 1 gene MP:0002898 absent cartilage IAGP N RGD:5509061 20141003 MGI PMID:8197187 1319762 Col9a1 collagen, type IX, alpha 1 gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20141003 MGI PMID:10595929 1319762 Col9a1 collagen, type IX, alpha 1 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:15802199 1319762 Col9a1 collagen, type IX, alpha 1 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:11680679 1319762 Col9a1 collagen, type IX, alpha 1 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:8197187 1319762 Col9a1 collagen, type IX, alpha 1 gene MP:0004591 enlarged tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:15802199 1319762 Col9a1 collagen, type IX, alpha 1 gene MP:0005353 abnormal patella morphology IAGP N RGD:5509061 20141003 MGI PMID:8197187 1319762 Col9a1 collagen, type IX, alpha 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:15802199 1319762 Col9a1 collagen, type IX, alpha 1 gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:8197187 1319762 Col9a1 collagen, type IX, alpha 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15802199 1319762 Col9a1 collagen, type IX, alpha 1 gene MP:0014091 abnormal tectorial membrane striated-sheet matrix morphology IAGP N RGD:5509061 20160421 MGI PMID:15802199 1319762 Col9a1 collagen, type IX, alpha 1 gene MP:0014100 increased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:8197187 1319762 Col9a1 collagen, type IX, alpha 1 gene MP:0030837 abnormal knee joint morphology IAGP N RGD:5509061 20181025 MGI PMID:8197187 1319764 Dsc2 desmocollin 2 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20170504 MGI 1319764 Dsc2 desmocollin 2 gene MP:0001314 cornea opacity IEA N RGD:5509061 20170504 MGI 1319764 Dsc2 desmocollin 2 gene MP:0001625 cardiac hypertrophy IEA N RGD:5509061 20210429 MGI 1319764 Dsc2 desmocollin 2 gene MP:0002625 heart left ventricle hypertrophy IEA N RGD:5509061 20210429 MGI 1319764 Dsc2 desmocollin 2 gene MP:0003141 cardiac fibrosis IEA N RGD:5509061 20210429 MGI 1319764 Dsc2 desmocollin 2 gene MP:0005287 narrow eye opening IEA N RGD:5509061 20170504 MGI 1319764 Dsc2 desmocollin 2 gene MP:0005542 cornea vascularization IEA N RGD:5509061 20170504 MGI 1319764 Dsc2 desmocollin 2 gene MP:0006042 increased apoptosis IEA N RGD:5509061 20210429 MGI 1319764 Dsc2 desmocollin 2 gene MP:0031633 decreased heart left ventricle muscle contractility IEA N RGD:5509061 20240704 MGI 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:21515572 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20210304 MGI PMID:31386652 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20210304 MGI PMID:31386652 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21515572 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:21515572 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:23727838 1319765 Tubb2b tubulin, beta 2B class IIB gene MP:0012448 abnormal primary motor cortex morphology IAGP N RGD:5509061 20210304 MGI PMID:31386652 1319768 Gsg1l GSG1-like gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200514 MGI 1319768 Gsg1l GSG1-like gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1319768 Gsg1l GSG1-like gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1319768 Gsg1l GSG1-like gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1319768 Gsg1l GSG1-like gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20201022 MGI 1319768 Gsg1l GSG1-like gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1319768 Gsg1l GSG1-like gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1319768 Gsg1l GSG1-like gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1319768 Gsg1l GSG1-like gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1319768 Gsg1l GSG1-like gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20210225 MGI PMID:32697982 1319768 Gsg1l GSG1-like gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20210225 MGI PMID:32697982 1319768 Gsg1l GSG1-like gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20210225 MGI PMID:32697982 1319768 Gsg1l GSG1-like gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20210225 MGI PMID:32697982 1319768 Gsg1l GSG1-like gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20210225 MGI PMID:32697982 1319768 Gsg1l GSG1-like gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20210225 MGI PMID:32697982 1319768 Gsg1l GSG1-like gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20210225 MGI PMID:32697982 1319768 Gsg1l GSG1-like gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1319768 Gsg1l GSG1-like gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 1319768 Gsg1l GSG1-like gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20210225 MGI PMID:32697982 1319768 Gsg1l GSG1-like gene MP:0011272 short excitatory postsynaptic current rise time IAGP N RGD:5509061 20210225 MGI PMID:32697982 1319768 Gsg1l GSG1-like gene MP:0011274 short excitatory postsynaptic current decay time IAGP N RGD:5509061 20210225 MGI PMID:32697982 1319771 Adgrb2 adhesion G protein-coupled receptor B2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20170105 MGI 1319771 Adgrb2 adhesion G protein-coupled receptor B2 gene MP:0003063 increased coping response IEA N RGD:5509061 20111116 MGI 1319775 Cyp2u1 cytochrome P450, family 2, subfamily u, polypeptide 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20201231 MGI 1319775 Cyp2u1 cytochrome P450, family 2, subfamily u, polypeptide 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1319775 Cyp2u1 cytochrome P450, family 2, subfamily u, polypeptide 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1319778 Nhp2 NHP2 ribonucleoprotein gene MP:0001257 increased body length IEA N RGD:5509061 20211021 MGI 1319778 Nhp2 NHP2 ribonucleoprotein gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20150108 MGI 1319778 Nhp2 NHP2 ribonucleoprotein gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20211021 MGI 1319778 Nhp2 NHP2 ribonucleoprotein gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1319778 Nhp2 NHP2 ribonucleoprotein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319780 Ndufs8 NADH:ubiquinone oxidoreductase core subunit S8 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191205 MGI 1319780 Ndufs8 NADH:ubiquinone oxidoreductase core subunit S8 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319780 Ndufs8 NADH:ubiquinone oxidoreductase core subunit S8 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191205 MGI 1319780 Ndufs8 NADH:ubiquinone oxidoreductase core subunit S8 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1319780 Ndufs8 NADH:ubiquinone oxidoreductase core subunit S8 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191205 MGI 1319780 Ndufs8 NADH:ubiquinone oxidoreductase core subunit S8 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191205 MGI 1319780 Ndufs8 NADH:ubiquinone oxidoreductase core subunit S8 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1319780 Ndufs8 NADH:ubiquinone oxidoreductase core subunit S8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319780 Ndufs8 NADH:ubiquinone oxidoreductase core subunit S8 gene MP:0012724 absent head fold IEA N RGD:5509061 20191205 MGI 1319780 Ndufs8 NADH:ubiquinone oxidoreductase core subunit S8 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191205 MGI 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:23546880 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:23546880 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20230420 MGI PMID:36062803 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:22972987 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23546880 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20230420 MGI PMID:36062803 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16260493 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:16260493 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22143887 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17085580 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001665 chronic diarrhea IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22348103 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0002816 colitis IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17085580 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22972987 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20141003 MGI PMID:22143887 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20230420 MGI PMID:36062803 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:22972987 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0004972 abnormal regulatory T cell number IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0004975 absent regulatory T cells IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20230420 MGI PMID:36062803 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20230420 MGI PMID:36062803 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16857737 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:22143887 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:22972987 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22972987 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16857737 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16857737 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16940043 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008350 increased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008399 abnormal alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:23546880 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22348103 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22348103 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20230420 MGI PMID:36062803 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:22348103 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:22348103 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22348103 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:22348103 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:22348103 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20230420 MGI PMID:36062803 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20230420 MGI PMID:36062803 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:22348103 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20230420 MGI PMID:36062803 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:22348103 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0008895 abnormal intraepithelial T cell number IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20230420 MGI PMID:36062803 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16857737 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0009623 enlarged inguinal lymph nodes IAGP N RGD:5509061 20230420 MGI PMID:36062803 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0009631 enlarged axillary lymph nodes IAGP N RGD:5509061 20230420 MGI PMID:36062803 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141003 MGI PMID:23546880 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22348103 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23546880 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:23546880 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:23546880 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0011009 increased circulating glutamate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:20478530 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23546880 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22348103 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16260493 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17085580 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22972987 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0011705 absent fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:16186825 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:16556914 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1319783 Map3k7 mitogen-activated protein kinase kinase kinase 7 gene MP:0014201 abnormal intestinal epithelium physiology IAGP N RGD:5509061 20170223 MGI PMID:26132627 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:5912439 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:23986237 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:16116426 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:20940229 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:23095888 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9545534 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9545534 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20230601 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23095888 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15637299 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:11440971 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11440971 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20230601 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000436 abnormal head movements IAGP N RGD:5509061 20141003 MGI PMID:5955164 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000436 abnormal head movements IAGP N RGD:5509061 20141003 MGI PMID:923728 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000445 short snout IAGP N RGD:5509061 20221201 MGI PMID:24689077 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:11401449 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:16571627 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:21404367 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:22363783 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:24203697 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:23696638 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:4230658 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20111116 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:4230658 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:923728 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:4230658 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:923728 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:1138408 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:1138408 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:14512015 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19008950 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20151001 MGI PMID:25128525 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:19008950 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11401449 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18257070 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:20940229 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:23359061 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:9545534 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20151001 MGI PMID:25128525 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:17566405 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:22363783 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20150924 MGI PMID:25218921 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:20223754 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20223754 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:22363783 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20151001 MGI PMID:25128525 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001391 abnormal tail movements IAGP N RGD:5509061 20141003 MGI PMID:5955164 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:5955164 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:5955164 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:16571627 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:18257070 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:9545534 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:9545534 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11401449 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11440971 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20151001 MGI PMID:25128525 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20220519 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21404367 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22363783 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20150924 MGI PMID:25218921 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17566405 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:5955164 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20151001 MGI PMID:25128525 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20151001 MGI PMID:25128525 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19008950 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23359061 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23986237 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20111116 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16571627 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21404367 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17566405 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002200 abnormal brain ventricular system morphology IAGP N RGD:5509061 20141003 MGI PMID:923728 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:5912439 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:16571627 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:8088438 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20151001 MGI PMID:25128525 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18606138 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20940229 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22363783 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20150924 MGI PMID:25218921 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002623 abnormal vestibular hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22363783 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:4230658 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:5955164 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002758 long tail IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:16571627 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:9545534 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:11401449 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:11707073 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:19701191 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:21404367 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:21515572 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:23359061 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:23696638 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:24203697 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20151001 MGI PMID:25128525 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003052 omphalocele IAGP N RGD:5509061 20151001 MGI PMID:25128525 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:11707073 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:15229603 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:18257070 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:19966784 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:20704721 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:21404367 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:22363783 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:24203697 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20221201 MGI PMID:36123354 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003126 abnormal external female genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:23986237 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:11401449 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20151001 MGI PMID:25128525 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003384 abnormal ventral body wall morphology IEA N RGD:5509061 20111229 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003385 abnormal body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003540 imperforate hymen IAGP N RGD:5509061 20141003 MGI PMID:21404367 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:20223754 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18604206 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:18606138 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:8088438 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23986237 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:4477997 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:18257070 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:19706528 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20141003 MGI PMID:23696638 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003938 abnormal ear development IEA N RGD:5509061 20111116 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003942 abnormal urinary system development IAGP N RGD:5509061 20141003 MGI PMID:23696638 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:19701191 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:4230658 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11440971 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:11440971 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004159 double aortic arch IAGP N RGD:5509061 20141003 MGI PMID:11440971 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:23359061 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23359061 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11401449 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23359061 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9545534 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004302 abnormal Deiters cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23986237 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004391 abnormal respiratory conducting tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20223754 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16571627 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18606138 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22363783 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22363783 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20150924 MGI PMID:25218921 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:22363783 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:19008950 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004406 abnormal cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:20940229 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004407 increased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16116426 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004407 increased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:19008950 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16116426 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16170314 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:20940229 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:21404367 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:22363783 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:23986237 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:24203697 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:23986237 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16116426 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:19008950 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20160128 MGI PMID:24135232 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:16170314 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:23986237 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23986237 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0005034 abnormal anus morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0005226 abnormal vertebral arch development IAGP N RGD:5509061 20141003 MGI PMID:9545534 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9545534 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0006014 dilated endolymphatic sac IAGP N RGD:5509061 20141003 MGI PMID:5912439 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0006026 dilated terminal bronchiole tube IAGP N RGD:5509061 20141003 MGI PMID:20223754 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:11401449 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:19008950 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20220630 MGI PMID:35440748 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0006286 inner ear hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19008950 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0006286 inner ear hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23986237 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20223754 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0006394 abnormal vertebral epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008149 abnormal costovertebral joint morphology IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008307 short scala media IAGP N RGD:5509061 20141003 MGI PMID:23986237 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:4230658 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:923728 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:923728 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:11401449 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:11707073 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:16571627 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:18257070 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:19008950 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:19701191 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:20223754 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:20704721 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:21404367 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:21515572 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:22363783 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:4477997 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:8088438 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:9545534 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20151001 MGI PMID:25128525 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0008933 abnormal motile primary cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0009199 abnormal external male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:21404367 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:23359061 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:17566405 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0009929 meningomyelocele IAGP N RGD:5509061 20141003 MGI PMID:17566405 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11440971 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20940229 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23095888 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0010466 vascular ring IAGP N RGD:5509061 20141003 MGI PMID:11440971 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0010488 abnormal left subclavian artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11440971 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0010589 common truncal valve IAGP N RGD:5509061 20141003 MGI PMID:11440971 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0010744 abnormal cervical flexure morphology IAGP N RGD:5509061 20141003 MGI PMID:11440971 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:20223754 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0010866 abnormal prenatal body size IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:20223754 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0010976 small lung lobe IAGP N RGD:5509061 20141003 MGI PMID:20223754 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:20223754 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011032 impaired branching involved in terminal bronchiole morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:20223754 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19966784 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16571627 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011088 neonatal lethality, incomplete penetrance IEA N RGD:5509061 20160421 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011089 perinatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23986237 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16170314 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20151001 MGI PMID:25128525 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16170314 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19966784 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20160421 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:20223754 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011172 abnormal otic pit morphology IAGP N RGD:5509061 20141003 MGI PMID:6650116 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22363783 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20230601 MGI 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:13435227 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23986237 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0012027 abnormal embryonic cilium location or orientation IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0012027 abnormal embryonic cilium location or orientation IAGP N RGD:5509061 20141003 MGI PMID:23406901 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20220630 MGI PMID:35440748 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0012304 short umbilical cord IAGP N RGD:5509061 20141003 MGI PMID:14039372 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0012675 enlarged floor plate IAGP N RGD:5509061 20141003 MGI PMID:11401449 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0012675 enlarged floor plate IAGP N RGD:5509061 20141003 MGI PMID:23359061 1319788 Vangl2 VANGL planar cell polarity 2 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20221201 MGI PMID:24689077 1319791 Bicd1 BICD cargo adaptor 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210805 MGI 1319791 Bicd1 BICD cargo adaptor 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210805 MGI 1319791 Bicd1 BICD cargo adaptor 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1319791 Bicd1 BICD cargo adaptor 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210805 MGI 1319796 Ltbr lymphotoxin B receptor gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20226692 1319796 Ltbr lymphotoxin B receptor gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:20226692 1319796 Ltbr lymphotoxin B receptor gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:9697836 1319796 Ltbr lymphotoxin B receptor gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:21441458 1319796 Ltbr lymphotoxin B receptor gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9697836 1319796 Ltbr lymphotoxin B receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9697836 1319796 Ltbr lymphotoxin B receptor gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20226692 1319796 Ltbr lymphotoxin B receptor gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:9697836 1319796 Ltbr lymphotoxin B receptor gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20141003 MGI 1319796 Ltbr lymphotoxin B receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22357629 1319796 Ltbr lymphotoxin B receptor gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:9697836 1319796 Ltbr lymphotoxin B receptor gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:21441458 1319796 Ltbr lymphotoxin B receptor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20226692 1319796 Ltbr lymphotoxin B receptor gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:22357629 1319796 Ltbr lymphotoxin B receptor gene MP:0002459 abnormal B cell physiology IEA N RGD:5509061 20141003 MGI 1319796 Ltbr lymphotoxin B receptor gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:14638845 1319796 Ltbr lymphotoxin B receptor gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21441458 1319796 Ltbr lymphotoxin B receptor gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:9697836 1319796 Ltbr lymphotoxin B receptor gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:9697836 1319796 Ltbr lymphotoxin B receptor gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20181004 MGI 1319796 Ltbr lymphotoxin B receptor gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9697836 1319796 Ltbr lymphotoxin B receptor gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9697836 1319796 Ltbr lymphotoxin B receptor gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9697836 1319796 Ltbr lymphotoxin B receptor gene MP:0005070 impaired natural killer cell mediated cytotoxicity IEA N RGD:5509061 20180927 MGI 1319796 Ltbr lymphotoxin B receptor gene MP:0008039 increased NK T cell number IEA N RGD:5509061 20180927 MGI 1319796 Ltbr lymphotoxin B receptor gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20181004 MGI 1319796 Ltbr lymphotoxin B receptor gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181004 MGI 1319796 Ltbr lymphotoxin B receptor gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181004 MGI 1319796 Ltbr lymphotoxin B receptor gene MP:0008083 decreased single-positive T cell number IEA N RGD:5509061 20181004 MGI 1319796 Ltbr lymphotoxin B receptor gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:9697836 1319796 Ltbr lymphotoxin B receptor gene MP:0008201 absent follicular dendritic cells IAGP N RGD:5509061 20141003 MGI PMID:21441458 1319796 Ltbr lymphotoxin B receptor gene MP:0008343 abnormal gamma-delta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21419662 1319796 Ltbr lymphotoxin B receptor gene MP:0008464 absent peripheral lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9697836 1319796 Ltbr lymphotoxin B receptor gene MP:0008465 absent mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21441458 1319796 Ltbr lymphotoxin B receptor gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9697836 1319796 Ltbr lymphotoxin B receptor gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:21441458 1319796 Ltbr lymphotoxin B receptor gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:16705172 1319796 Ltbr lymphotoxin B receptor gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:21419662 1319796 Ltbr lymphotoxin B receptor gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:20226692 1319796 Ltbr lymphotoxin B receptor gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21441458 1319796 Ltbr lymphotoxin B receptor gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20226692 1319796 Ltbr lymphotoxin B receptor gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20181004 MGI 1319796 Ltbr lymphotoxin B receptor gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20150326 MGI PMID:21441458 1319796 Ltbr lymphotoxin B receptor gene MP:0020174 abnormal IgG level IEA N RGD:5509061 20180215 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20160804 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12217959 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20963592 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12217959 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:20963592 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20160804 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:15256493 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12217959 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:21467199 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:15256493 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:20963592 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:23100620 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0002492 decreased IgE level IEA N RGD:5509061 20160804 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20210128 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160421 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20201022 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20220519 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0003673 abnormal inguinal canal morphology IAGP N RGD:5509061 20141003 MGI PMID:12217959 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20220519 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:20963592 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:20963592 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0005149 abnormal gubernaculum morphology IAGP N RGD:5509061 20141003 MGI PMID:12217959 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:12217959 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0005573 increased pulmonary respiratory rate IEA N RGD:5509061 20220811 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160421 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20160421 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0009082 uterus cyst IAGP N RGD:5509061 20141003 MGI PMID:21467199 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0009213 absent male inguinal canal IAGP N RGD:5509061 20141003 MGI PMID:12217959 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0009251 enlarged endometrial glands IAGP N RGD:5509061 20141003 MGI PMID:21467199 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20220519 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20141003 MGI PMID:21467199 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20201022 MGI 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0013401 increased endometrial gland number IAGP N RGD:5509061 20141218 MGI PMID:21467199 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0013713 decreased nipple size IAGP N RGD:5509061 20150402 MGI PMID:15256493 1319798 Rxfp2 relaxin/insulin-like family peptide receptor 2 gene MP:0031287 bilateral cryptorchism IAGP N RGD:5509061 20211014 MGI PMID:12217959 1319799 Ppp4r3b protein phosphatase 4 regulatory subunit 3B gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1319799 Ppp4r3b protein phosphatase 4 regulatory subunit 3B gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1319799 Ppp4r3b protein phosphatase 4 regulatory subunit 3B gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1319799 Ppp4r3b protein phosphatase 4 regulatory subunit 3B gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1319799 Ppp4r3b protein phosphatase 4 regulatory subunit 3B gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1319799 Ppp4r3b protein phosphatase 4 regulatory subunit 3B gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210520 MGI 1319799 Ppp4r3b protein phosphatase 4 regulatory subunit 3B gene MP:0001406 abnormal gait IEA N RGD:5509061 20230601 MGI 1319799 Ppp4r3b protein phosphatase 4 regulatory subunit 3B gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1319799 Ppp4r3b protein phosphatase 4 regulatory subunit 3B gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210128 MGI 1319799 Ppp4r3b protein phosphatase 4 regulatory subunit 3B gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20200514 MGI 1319799 Ppp4r3b protein phosphatase 4 regulatory subunit 3B gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20210128 MGI 1319801 Sec24a SEC24 homolog A, COPII coat complex component gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319801 Sec24a SEC24 homolog A, COPII coat complex component gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1319801 Sec24a SEC24 homolog A, COPII coat complex component gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319801 Sec24a SEC24 homolog A, COPII coat complex component gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1319801 Sec24a SEC24 homolog A, COPII coat complex component gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20160804 MGI 1319801 Sec24a SEC24 homolog A, COPII coat complex component gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1319801 Sec24a SEC24 homolog A, COPII coat complex component gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319801 Sec24a SEC24 homolog A, COPII coat complex component gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20160804 MGI 1319801 Sec24a SEC24 homolog A, COPII coat complex component gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0001196 shiny skin IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0001263 weight loss IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0009474 thick epidermis stratum spinosum IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0009596 abnormal stratum corneum lipid matrix formation IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0009602 abnormal keratohyalin granule morphology IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0009604 increased keratohyalin granule number IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0009607 decreased keratohyalin granule size IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0011979 abnormal magnesium ion homeostasis IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0020116 increased sphingosine level IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0020117 decreased sphingosine level IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0020582 increased ceramide level IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0020583 decreased ceramide level IAGP N RGD:5509061 20180621 MGI PMID:29174370 1319802 Nipal4 NIPA-like domain containing 4 gene MP:0030605 abnormal corneocyte morphology IAGP N RGD:5509061 20180628 MGI PMID:29174370 1319803 Lrrc71 leucine rich repeat containing 71 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1319805 Lix1 limb and CNS expressed 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21846745 1319807 Stk38 serine/threonine kinase 38 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1319807 Stk38 serine/threonine kinase 38 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20190905 MGI PMID:30135513 1319807 Stk38 serine/threonine kinase 38 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20181206 MGI PMID:20551432 1319807 Stk38 serine/threonine kinase 38 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20160602 MGI PMID:25981615 1319807 Stk38 serine/threonine kinase 38 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20181206 MGI PMID:20551432 1319807 Stk38 serine/threonine kinase 38 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1319807 Stk38 serine/threonine kinase 38 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20181206 MGI PMID:20551432 1319807 Stk38 serine/threonine kinase 38 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20181206 MGI PMID:20551432 1319807 Stk38 serine/threonine kinase 38 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1319807 Stk38 serine/threonine kinase 38 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20160602 MGI PMID:25981615 1319807 Stk38 serine/threonine kinase 38 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20190905 MGI PMID:30135513 1319807 Stk38 serine/threonine kinase 38 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20190905 MGI PMID:30135513 1319807 Stk38 serine/threonine kinase 38 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1319807 Stk38 serine/threonine kinase 38 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20190905 MGI PMID:30135513 1319807 Stk38 serine/threonine kinase 38 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20160602 MGI PMID:25981615 1319807 Stk38 serine/threonine kinase 38 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20160602 MGI PMID:25981615 1319807 Stk38 serine/threonine kinase 38 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20160602 MGI PMID:25981615 1319807 Stk38 serine/threonine kinase 38 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20160602 MGI PMID:25981615 1319807 Stk38 serine/threonine kinase 38 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20181206 MGI PMID:20551432 1319807 Stk38 serine/threonine kinase 38 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20181206 MGI PMID:20551432 1319807 Stk38 serine/threonine kinase 38 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20160602 MGI PMID:25981615 1319807 Stk38 serine/threonine kinase 38 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20160602 MGI PMID:25981615 1319807 Stk38 serine/threonine kinase 38 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1319807 Stk38 serine/threonine kinase 38 gene MP:0011996 abnormal retina inner nuclear layer thickness IAGP N RGD:5509061 20190905 MGI PMID:30135513 1319807 Stk38 serine/threonine kinase 38 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1319807 Stk38 serine/threonine kinase 38 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20190905 MGI PMID:30135513 1319811 Glyr1 glyoxylate reductase 1 homolog (Arabidopsis) gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1319811 Glyr1 glyoxylate reductase 1 homolog (Arabidopsis) gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20210520 MGI 1319811 Glyr1 glyoxylate reductase 1 homolog (Arabidopsis) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1319811 Glyr1 glyoxylate reductase 1 homolog (Arabidopsis) gene MP:0002764 short tibia IEA N RGD:5509061 20210520 MGI 1319811 Glyr1 glyoxylate reductase 1 homolog (Arabidopsis) gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20210520 MGI 1319811 Glyr1 glyoxylate reductase 1 homolog (Arabidopsis) gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20221215 MGI 1319811 Glyr1 glyoxylate reductase 1 homolog (Arabidopsis) gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20210520 MGI 1319811 Glyr1 glyoxylate reductase 1 homolog (Arabidopsis) gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210826 MGI 1319811 Glyr1 glyoxylate reductase 1 homolog (Arabidopsis) gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20210520 MGI 1319811 Glyr1 glyoxylate reductase 1 homolog (Arabidopsis) gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20220602 MGI PMID:35182466 1319811 Glyr1 glyoxylate reductase 1 homolog (Arabidopsis) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20220602 MGI PMID:35182466 1319811 Glyr1 glyoxylate reductase 1 homolog (Arabidopsis) gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20220602 MGI PMID:35182466 1319813 Rigi RNA sensor RIG-I gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18650396 1319813 Rigi RNA sensor RIG-I gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18650396 1319813 Rigi RNA sensor RIG-I gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 1319813 Rigi RNA sensor RIG-I gene MP:0000601 small liver IEA N RGD:5509061 20230601 MGI 1319813 Rigi RNA sensor RIG-I gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18650396 1319813 Rigi RNA sensor RIG-I gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17893708 1319813 Rigi RNA sensor RIG-I gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1319813 Rigi RNA sensor RIG-I gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:17893708 1319813 Rigi RNA sensor RIG-I gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1319813 Rigi RNA sensor RIG-I gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16039576 1319813 Rigi RNA sensor RIG-I gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18650396 1319813 Rigi RNA sensor RIG-I gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16625202 1319813 Rigi RNA sensor RIG-I gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18650396 1319813 Rigi RNA sensor RIG-I gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18650396 1319813 Rigi RNA sensor RIG-I gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:17893708 1319813 Rigi RNA sensor RIG-I gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:16039576 1319813 Rigi RNA sensor RIG-I gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17893708 1319813 Rigi RNA sensor RIG-I gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230601 MGI 1319813 Rigi RNA sensor RIG-I gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:18650396 1319813 Rigi RNA sensor RIG-I gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16625202 1319813 Rigi RNA sensor RIG-I gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:17893708 1319813 Rigi RNA sensor RIG-I gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:17893708 1319813 Rigi RNA sensor RIG-I gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:17893708 1319813 Rigi RNA sensor RIG-I gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:17893708 1319813 Rigi RNA sensor RIG-I gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:16625202 1319813 Rigi RNA sensor RIG-I gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:16625202 1319813 Rigi RNA sensor RIG-I gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16039576 1319813 Rigi RNA sensor RIG-I gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16039576 1319813 Rigi RNA sensor RIG-I gene MP:0031044 increased susceptibility to Flaviviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:16625202 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20201022 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0000433 microcephaly IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0000537 abnormal urethra morphology IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0000823 abnormal lateral ventricle morphology IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0000961 abnormal dorsal root ganglion morphology IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0001260 increased body weight IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0001260 increased body weight IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0001261 obese IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0001634 internal hemorrhage IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0001914 hemorrhage IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0001925 male infertility IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20200402 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20200402 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0002947 increased hemangioma incidence IEA N RGD:5509061 20210930 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20200402 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0005655 increased aggression IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0008347 decreased gamma-delta T cell number IEA N RGD:5509061 20170105 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0008923 thoracoschisis IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0009493 abnormal cystic duct morphology IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0010490 abnormal inferior vena cava valve morphology IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0010602 abnormal pulmonary valve cusp morphology IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0012450 decreased primary motor cortex size IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0012466 decreased hippocampal fimbria size IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0012467 increased striatum size IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0012474 decreased cingulate cortex size IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0012768 decreased KLRG1-positive NK cell number IEA N RGD:5509061 20201231 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0013022 increased Ly6C high monocyte number IEA N RGD:5509061 20201022 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0013025 increased Ly6C low monocyte number IEA N RGD:5509061 20200402 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0013648 increased CD11b-high dendritic cell number IEA N RGD:5509061 20201231 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0013652 decreased CD11b-low dendritic cell number IEA N RGD:5509061 20201231 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0013968 multiple persisting craniopharyngeal ducts IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0020083 decreased hippocampus volume IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0020396 abnormal social recognition IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0020527 small thalamus IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0020543 decreased substantia nigra size IAGP N RGD:5509061 20210708 MGI PMID:32877400 1319814 Trappc9 trafficking protein particle complex 9 gene MP:0030003 hippocampus atrophy IAGP N RGD:5509061 20210617 MGI PMID:33208359 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20180215 MGI PMID:10675334 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12676787 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12676787 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12676787 1319819 Sp3 trans-acting transcription factor 3 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10675334 1319819 Sp3 trans-acting transcription factor 3 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12676787 1319819 Sp3 trans-acting transcription factor 3 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:10675334 1319819 Sp3 trans-acting transcription factor 3 gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:10675334 1319819 Sp3 trans-acting transcription factor 3 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12676787 1319819 Sp3 trans-acting transcription factor 3 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21085687 1319819 Sp3 trans-acting transcription factor 3 gene MP:0008958 abnormal trophoblast glycogen cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:10675334 1319819 Sp3 trans-acting transcription factor 3 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11472836 1319819 Sp3 trans-acting transcription factor 3 gene MP:0010128 hypovolemia IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10675334 1319819 Sp3 trans-acting transcription factor 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0011525 abnormal placenta intervillous maternal lacunae morphology IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0011527 disorganized placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0012109 decreased trophoblast glycogen cell number IAGP N RGD:5509061 20141003 MGI PMID:17584888 1319819 Sp3 trans-acting transcription factor 3 gene MP:0030542 abnormal dentin development IAGP N RGD:5509061 20180215 MGI PMID:10675334 1319819 Sp3 trans-acting transcription factor 3 gene MP:0030544 abnormal enamel development IAGP N RGD:5509061 20180215 MGI PMID:10675334 1319819 Sp3 trans-acting transcription factor 3 gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20191219 MGI PMID:17584888 1319821 Exo1 exonuclease 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:23254285 1319821 Exo1 exonuclease 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0008967 absent chiasmata formation IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0009564 abnormal meiotic configurations IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0009797 abnormal mismatch repair IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0009797 abnormal mismatch repair IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0010094 abnormal chromosome stability IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12629043 1319821 Exo1 exonuclease 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23754438 1319821 Exo1 exonuclease 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:12629043 1319824 Trem1 triggering receptor expressed on myeloid cells 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22719066 1319824 Trem1 triggering receptor expressed on myeloid cells 1 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22719066 1319824 Trem1 triggering receptor expressed on myeloid cells 1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22719066 1319824 Trem1 triggering receptor expressed on myeloid cells 1 gene MP:0004794 increased anti-nuclear antigen antibody level IEA N RGD:5509061 20201022 MGI 1319824 Trem1 triggering receptor expressed on myeloid cells 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22719066 1319824 Trem1 triggering receptor expressed on myeloid cells 1 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22719066 1319826 Top3b topoisomerase (DNA) III beta gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11331780 1319826 Top3b topoisomerase (DNA) III beta gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11331780 1319826 Top3b topoisomerase (DNA) III beta gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11331780 1319826 Top3b topoisomerase (DNA) III beta gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:11331780 1319826 Top3b topoisomerase (DNA) III beta gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11331780 1319826 Top3b topoisomerase (DNA) III beta gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:11331780 1319826 Top3b topoisomerase (DNA) III beta gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:11331780 1319826 Top3b topoisomerase (DNA) III beta gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12591952 1319826 Top3b topoisomerase (DNA) III beta gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12591952 1319826 Top3b topoisomerase (DNA) III beta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11331780 1319826 Top3b topoisomerase (DNA) III beta gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11331780 1319826 Top3b topoisomerase (DNA) III beta gene MP:0002742 enlarged submandibular lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11331780 1319826 Top3b topoisomerase (DNA) III beta gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:11331780 1319826 Top3b topoisomerase (DNA) III beta gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:12591952 1319826 Top3b topoisomerase (DNA) III beta gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12591952 1319826 Top3b topoisomerase (DNA) III beta gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11331780 1319826 Top3b topoisomerase (DNA) III beta gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:12591952 1319826 Top3b topoisomerase (DNA) III beta gene MP:0009631 enlarged axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11331780 1319829 Ubxn1 UBX domain protein 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1319829 Ubxn1 UBX domain protein 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1319829 Ubxn1 UBX domain protein 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1319830 Slc46a1 solute carrier family 46, member 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1319830 Slc46a1 solute carrier family 46, member 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 1319830 Slc46a1 solute carrier family 46, member 1 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20211021 MGI 1319830 Slc46a1 solute carrier family 46, member 1 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:19204075 1319830 Slc46a1 solute carrier family 46, member 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220519 MGI 1319830 Slc46a1 solute carrier family 46, member 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220519 MGI 1319830 Slc46a1 solute carrier family 46, member 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170105 MGI 1319830 Slc46a1 solute carrier family 46, member 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20220519 MGI 1319830 Slc46a1 solute carrier family 46, member 1 gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20180920 MGI PMID:19204075 1319834 Stard4 StAR related lipid transfer domain containing 4 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19965609 1319834 Stard4 StAR related lipid transfer domain containing 4 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19965609 1319834 Stard4 StAR related lipid transfer domain containing 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19965609 1319834 Stard4 StAR related lipid transfer domain containing 4 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19965609 1319834 Stard4 StAR related lipid transfer domain containing 4 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:19965609 1319834 Stard4 StAR related lipid transfer domain containing 4 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19965609 1319836 Trim8 tripartite motif-containing 8 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1319836 Trim8 tripartite motif-containing 8 gene MP:0001257 increased body length IEA N RGD:5509061 20210128 MGI 1319836 Trim8 tripartite motif-containing 8 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20211202 MGI PMID:28747347 1319836 Trim8 tripartite motif-containing 8 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1319836 Trim8 tripartite motif-containing 8 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1319836 Trim8 tripartite motif-containing 8 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1319836 Trim8 tripartite motif-containing 8 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20211202 MGI PMID:28747347 1319836 Trim8 tripartite motif-containing 8 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20211202 MGI PMID:28747347 1319836 Trim8 tripartite motif-containing 8 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20211202 MGI PMID:28747347 1319836 Trim8 tripartite motif-containing 8 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20211202 MGI PMID:28747347 1319836 Trim8 tripartite motif-containing 8 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20211202 MGI PMID:28747347 1319836 Trim8 tripartite motif-containing 8 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20211202 MGI PMID:28747347 1319836 Trim8 tripartite motif-containing 8 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20211202 MGI PMID:28747347 1319836 Trim8 tripartite motif-containing 8 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20211202 MGI PMID:28747347 1319836 Trim8 tripartite motif-containing 8 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20211202 MGI PMID:28747347 1319836 Trim8 tripartite motif-containing 8 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20211202 MGI PMID:28747347 1319836 Trim8 tripartite motif-containing 8 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210429 MGI PMID:27956576 1319836 Trim8 tripartite motif-containing 8 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210506 MGI PMID:31360105 1319836 Trim8 tripartite motif-containing 8 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20211202 MGI PMID:28747347 1319836 Trim8 tripartite motif-containing 8 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20211202 MGI PMID:28747347 1319836 Trim8 tripartite motif-containing 8 gene MP:0011078 increased macrophage cytokine production IAGP N RGD:5509061 20211202 MGI PMID:28747347 1319838 Polr2b polymerase (RNA) II (DNA directed) polypeptide B gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20241010 MGI 1319838 Polr2b polymerase (RNA) II (DNA directed) polypeptide B gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241010 MGI 1319838 Polr2b polymerase (RNA) II (DNA directed) polypeptide B gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241010 MGI 1319838 Polr2b polymerase (RNA) II (DNA directed) polypeptide B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1319838 Polr2b polymerase (RNA) II (DNA directed) polypeptide B gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20241010 MGI 1319843 Ints6 integrator complex subunit 6 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20141003 MGI 1319852 Bcl7a B cell CLL/lymphoma 7A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191017 MGI PMID:29213114 1319852 Bcl7a B cell CLL/lymphoma 7A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20191017 MGI PMID:29213114 1319852 Bcl7a B cell CLL/lymphoma 7A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20191017 MGI PMID:29213114 1319852 Bcl7a B cell CLL/lymphoma 7A gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1319852 Bcl7a B cell CLL/lymphoma 7A gene MP:0001522 impaired swimming IAGP N RGD:5509061 20191017 MGI PMID:29213114 1319852 Bcl7a B cell CLL/lymphoma 7A gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1319852 Bcl7a B cell CLL/lymphoma 7A gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20231109 MGI PMID:36325906 1319852 Bcl7a B cell CLL/lymphoma 7A gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20191017 MGI PMID:29213114 1319852 Bcl7a B cell CLL/lymphoma 7A gene MP:0008823 abnormal interventricular septum membranous part morphology IAGP N RGD:5509061 20231109 MGI PMID:36325906 1319852 Bcl7a B cell CLL/lymphoma 7A gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20231109 MGI PMID:36325906 1319852 Bcl7a B cell CLL/lymphoma 7A gene MP:0010498 abnormal interventricular septum muscular part morphology IAGP N RGD:5509061 20231109 MGI PMID:36325906 1319852 Bcl7a B cell CLL/lymphoma 7A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319852 Bcl7a B cell CLL/lymphoma 7A gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20191017 MGI PMID:29213114 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:18477811 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:8614465 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16109771 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16109771 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:18064674 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:16109771 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:18477811 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16109771 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:16109771 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000774 decreased brain size IEA N RGD:5509061 20230119 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20147379 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:20147379 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001017 abnormal stellate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20147379 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:20147379 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230119 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20231207 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:20147379 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16109771 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:18064674 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18477811 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:8614465 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8614465 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230119 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18064674 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:8614465 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:8614465 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:18064674 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18477811 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:18477811 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:8614465 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20231207 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:16109771 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:18477811 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0003201 extremity edema IAGP N RGD:5509061 20141003 MGI PMID:18477811 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:9815146 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16109771 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18477811 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20230119 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:20147379 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9815146 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16109771 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:18477811 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0004323 sternum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0004573 absent limb buds IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20230119 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20230119 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:16109771 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0005252 abnormal Meibomian gland morphology IAGP N RGD:5509061 20141003 MGI PMID:20147379 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18477811 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20230119 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0008068 absent retina ganglion cell IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:8614465 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0008510 absent retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0008514 absent retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0009284 abnormal sympathetic neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:20147379 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20230119 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0010395 abnormal pharyngeal arch development IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16109771 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:8614465 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:16109771 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0010417 subarterial ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18477811 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:8614465 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0010500 myocardium hypoplasia IAGP N RGD:5509061 20240125 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0010572 persistent right dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:9815146 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:9815146 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0010645 failure of conotruncal ridge closure IAGP N RGD:5509061 20141003 MGI PMID:8614465 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0010650 abnormal aorticopulmonary septum morphology IAGP N RGD:5509061 20141003 MGI PMID:8614465 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16109771 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18064674 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18477811 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8614465 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0011261 abnormal limb mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0011262 abnormal pharyngeal arch mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:23649630 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:20596238 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0031553 abnormal semilunar valve development IAGP N RGD:5509061 20240125 MGI PMID:18064674 1319855 Sox4 SRY (sex determining region Y)-box 4 gene MP:0031583 semilunar valve hypoplasia IAGP N RGD:5509061 20240125 MGI PMID:20596238 1319862 Rps6kl1 ribosomal protein S6 kinase-like 1 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220811 MGI 1319862 Rps6kl1 ribosomal protein S6 kinase-like 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1319862 Rps6kl1 ribosomal protein S6 kinase-like 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220811 MGI 1319865 Srsf9 serine and arginine-rich splicing factor 9 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1319865 Srsf9 serine and arginine-rich splicing factor 9 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 1319866 Alkbh5 alkB homolog 5, RNA demethylase gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23177736 1319866 Alkbh5 alkB homolog 5, RNA demethylase gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23177736 1319866 Alkbh5 alkB homolog 5, RNA demethylase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23177736 1319866 Alkbh5 alkB homolog 5, RNA demethylase gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23177736 1319866 Alkbh5 alkB homolog 5, RNA demethylase gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23177736 1319866 Alkbh5 alkB homolog 5, RNA demethylase gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23177736 1319866 Alkbh5 alkB homolog 5, RNA demethylase gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23177736 1319866 Alkbh5 alkB homolog 5, RNA demethylase gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23177736 1319868 Efnb2 ephrin B2 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16968134 1319868 Efnb2 ephrin B2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21539827 1319868 Efnb2 ephrin B2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:11880349 1319868 Efnb2 ephrin B2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:15466160 1319868 Efnb2 ephrin B2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11163240 1319868 Efnb2 ephrin B2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11880349 1319868 Efnb2 ephrin B2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19571816 1319868 Efnb2 ephrin B2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:9630219 1319868 Efnb2 ephrin B2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:11880349 1319868 Efnb2 ephrin B2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11880349 1319868 Efnb2 ephrin B2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9630219 1319868 Efnb2 ephrin B2 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:11163240 1319868 Efnb2 ephrin B2 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:11880349 1319868 Efnb2 ephrin B2 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:9630219 1319868 Efnb2 ephrin B2 gene MP:0000380 small hair follicles IAGP N RGD:5509061 20141003 MGI PMID:19571816 1319868 Efnb2 ephrin B2 gene MP:0000424 retarded hair growth IAGP N RGD:5509061 20141003 MGI PMID:19571816 1319868 Efnb2 ephrin B2 gene MP:0000537 abnormal urethra morphology IAGP N RGD:5509061 20141003 MGI PMID:15223334 1319868 Efnb2 ephrin B2 gene MP:0000618 small salivary gland IAGP N RGD:5509061 20141003 MGI PMID:17223098 1319868 Efnb2 ephrin B2 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:17223098 1319868 Efnb2 ephrin B2 gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:19571816 1319868 Efnb2 ephrin B2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:19571816 1319868 Efnb2 ephrin B2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:19571816 1319868 Efnb2 ephrin B2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:17158005 1319868 Efnb2 ephrin B2 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:17158005 1319868 Efnb2 ephrin B2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:14699416 1319868 Efnb2 ephrin B2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:17223098 1319868 Efnb2 ephrin B2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11880349 1319868 Efnb2 ephrin B2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11880349 1319868 Efnb2 ephrin B2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19571816 1319868 Efnb2 ephrin B2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15687262 1319868 Efnb2 ephrin B2 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:14699416 1319868 Efnb2 ephrin B2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15223334 1319868 Efnb2 ephrin B2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15687262 1319868 Efnb2 ephrin B2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21539827 1319868 Efnb2 ephrin B2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11163240 1319868 Efnb2 ephrin B2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17223098 1319868 Efnb2 ephrin B2 gene MP:0002349 abnormal afferent lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15687262 1319868 Efnb2 ephrin B2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:17158005 1319868 Efnb2 ephrin B2 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:11163240 1319868 Efnb2 ephrin B2 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17223098 1319868 Efnb2 ephrin B2 gene MP:0003124 hypospadia IAGP N RGD:5509061 20141003 MGI PMID:15223334 1319868 Efnb2 ephrin B2 gene MP:0003124 hypospadia IAGP N RGD:5509061 20141003 MGI PMID:21539827 1319868 Efnb2 ephrin B2 gene MP:0003125 abnormal septation of the cloaca IAGP N RGD:5509061 20141003 MGI PMID:15223334 1319868 Efnb2 ephrin B2 gene MP:0003128 splayed clitoris IAGP N RGD:5509061 20141003 MGI PMID:15223334 1319868 Efnb2 ephrin B2 gene MP:0003129 persistent cloaca IAGP N RGD:5509061 20141003 MGI PMID:15223334 1319868 Efnb2 ephrin B2 gene MP:0003130 anal atresia IAGP N RGD:5509061 20141003 MGI PMID:15223334 1319868 Efnb2 ephrin B2 gene MP:0003164 decreased posterior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:17158005 1319868 Efnb2 ephrin B2 gene MP:0003166 decreased superior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:17158005 1319868 Efnb2 ephrin B2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11880349 1319868 Efnb2 ephrin B2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9630219 1319868 Efnb2 ephrin B2 gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:21539827 1319868 Efnb2 ephrin B2 gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20141003 MGI PMID:15687262 1319868 Efnb2 ephrin B2 gene MP:0003660 chylothorax IAGP N RGD:5509061 20141003 MGI PMID:15687262 1319868 Efnb2 ephrin B2 gene MP:0003840 abnormal coronal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:16968134 1319868 Efnb2 ephrin B2 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:9630219 1319868 Efnb2 ephrin B2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11163240 1319868 Efnb2 ephrin B2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9630219 1319868 Efnb2 ephrin B2 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:11163240 1319868 Efnb2 ephrin B2 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0004126 thin hypodermis IAGP N RGD:5509061 20141003 MGI PMID:19571816 1319868 Efnb2 ephrin B2 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:11163240 1319868 Efnb2 ephrin B2 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:9630219 1319868 Efnb2 ephrin B2 gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:11163240 1319868 Efnb2 ephrin B2 gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:11880349 1319868 Efnb2 ephrin B2 gene MP:0004885 abnormal endolymph physiology IAGP N RGD:5509061 20141003 MGI PMID:17158005 1319868 Efnb2 ephrin B2 gene MP:0004887 decreased endolymph production IAGP N RGD:5509061 20141003 MGI PMID:17158005 1319868 Efnb2 ephrin B2 gene MP:0004922 abnormal common crus morphology IAGP N RGD:5509061 20141003 MGI PMID:17158005 1319868 Efnb2 ephrin B2 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0005187 abnormal penis morphology IAGP N RGD:5509061 20141003 MGI PMID:15223334 1319868 Efnb2 ephrin B2 gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20141003 MGI PMID:15223334 1319868 Efnb2 ephrin B2 gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:17223098 1319868 Efnb2 ephrin B2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17336907 1319868 Efnb2 ephrin B2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17336907 1319868 Efnb2 ephrin B2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:21847105 1319868 Efnb2 ephrin B2 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:19571816 1319868 Efnb2 ephrin B2 gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:17158005 1319868 Efnb2 ephrin B2 gene MP:0006014 dilated endolymphatic sac IAGP N RGD:5509061 20141003 MGI PMID:17158005 1319868 Efnb2 ephrin B2 gene MP:0006338 abnormal second pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11163240 1319868 Efnb2 ephrin B2 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:17223098 1319868 Efnb2 ephrin B2 gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11163240 1319868 Efnb2 ephrin B2 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11163240 1319868 Efnb2 ephrin B2 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11163240 1319868 Efnb2 ephrin B2 gene MP:0006389 abnormal vestibular endolymph physiology IAGP N RGD:5509061 20141003 MGI PMID:17158005 1319868 Efnb2 ephrin B2 gene MP:0006391 abnormal vestibular endolymph ionic homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17158005 1319868 Efnb2 ephrin B2 gene MP:0008066 small endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:17158005 1319868 Efnb2 ephrin B2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:17223098 1319868 Efnb2 ephrin B2 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:17223098 1319868 Efnb2 ephrin B2 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:11880349 1319868 Efnb2 ephrin B2 gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0010591 enlarged aortic valve IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0010600 enlarged pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0010617 thick mitral valve cusps IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0010860 abnormal anterior commissure pars posterior morphology IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15687262 1319868 Efnb2 ephrin B2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19571816 1319868 Efnb2 ephrin B2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15223334 1319868 Efnb2 ephrin B2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21539827 1319868 Efnb2 ephrin B2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16968134 1319868 Efnb2 ephrin B2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11163240 1319868 Efnb2 ephrin B2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11880349 1319868 Efnb2 ephrin B2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17223098 1319868 Efnb2 ephrin B2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9630219 1319868 Efnb2 ephrin B2 gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11163240 1319868 Efnb2 ephrin B2 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11880349 1319868 Efnb2 ephrin B2 gene MP:0012493 absent pharyngeal arch arteries IAGP N RGD:5509061 20141003 MGI PMID:11163240 1319868 Efnb2 ephrin B2 gene MP:0012755 decreased cranial neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:17223098 1319868 Efnb2 ephrin B2 gene MP:0012757 abnormal cranial neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:17223098 1319868 Efnb2 ephrin B2 gene MP:0012761 increased cranial neural crest cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17223098 1319868 Efnb2 ephrin B2 gene MP:0013012 abnormal trunk neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:17223098 1319868 Efnb2 ephrin B2 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:21976681 1319868 Efnb2 ephrin B2 gene MP:0031529 pulmonary valve hyperplasia IAGP N RGD:5509061 20240104 MGI PMID:15223333 1319868 Efnb2 ephrin B2 gene MP:0031568 aortic valve hyperplasia IAGP N RGD:5509061 20240125 MGI PMID:15223333 1319870 Pigo phosphatidylinositol glycan anchor biosynthesis, class O gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20211021 MGI 1319870 Pigo phosphatidylinositol glycan anchor biosynthesis, class O gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20211021 MGI 1319870 Pigo phosphatidylinositol glycan anchor biosynthesis, class O gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319870 Pigo phosphatidylinositol glycan anchor biosynthesis, class O gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1319872 Dok1 docking protein 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15611294 1319872 Dok1 docking protein 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15611295 1319872 Dok1 docking protein 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20139980 1319872 Dok1 docking protein 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15611294 1319872 Dok1 docking protein 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15611295 1319872 Dok1 docking protein 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15611294 1319872 Dok1 docking protein 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15611295 1319872 Dok1 docking protein 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15611294 1319872 Dok1 docking protein 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:15611295 1319872 Dok1 docking protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15611294 1319872 Dok1 docking protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15611295 1319872 Dok1 docking protein 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15611294 1319872 Dok1 docking protein 1 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:15611294 1319872 Dok1 docking protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18204460 1319872 Dok1 docking protein 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15611294 1319872 Dok1 docking protein 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10640270 1319872 Dok1 docking protein 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20548287 1319872 Dok1 docking protein 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:15611294 1319872 Dok1 docking protein 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:15611295 1319872 Dok1 docking protein 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20139980 1319872 Dok1 docking protein 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15611294 1319872 Dok1 docking protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15611294 1319872 Dok1 docking protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15611295 1319872 Dok1 docking protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20139980 1319872 Dok1 docking protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20548287 1319872 Dok1 docking protein 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:20139980 1319872 Dok1 docking protein 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:11489947 1319872 Dok1 docking protein 1 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15611294 1319872 Dok1 docking protein 1 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15611295 1319872 Dok1 docking protein 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20548287 1319872 Dok1 docking protein 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18204460 1319872 Dok1 docking protein 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:18204460 1319872 Dok1 docking protein 1 gene MP:0004202 pulmonary hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20139980 1319872 Dok1 docking protein 1 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11489947 1319872 Dok1 docking protein 1 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10640270 1319872 Dok1 docking protein 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:18204460 1319872 Dok1 docking protein 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18204460 1319872 Dok1 docking protein 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:20548287 1319872 Dok1 docking protein 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18204460 1319872 Dok1 docking protein 1 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:20139980 1319872 Dok1 docking protein 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18204460 1319872 Dok1 docking protein 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20139980 1319872 Dok1 docking protein 1 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15611294 1319872 Dok1 docking protein 1 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18204460 1319872 Dok1 docking protein 1 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20160414 MGI PMID:18204460 1319872 Dok1 docking protein 1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20160414 MGI PMID:18204460 1319872 Dok1 docking protein 1 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20160414 MGI PMID:18204460 1319872 Dok1 docking protein 1 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20548287 1319872 Dok1 docking protein 1 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:18204460 1319872 Dok1 docking protein 1 gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:20139980 1319872 Dok1 docking protein 1 gene MP:0010829 increased bronchioalveolar stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20139980 1319872 Dok1 docking protein 1 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:15611294 1319872 Dok1 docking protein 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:11489947 1319872 Dok1 docking protein 1 gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:18204460 1319872 Dok1 docking protein 1 gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:18204460 1319874 Celf3 CUGBP, Elav-like family member 3 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:17393433 1319874 Celf3 CUGBP, Elav-like family member 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17393433 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0003125 abnormal septation of the cloaca IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0004017 duplex kidney IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0006130 pulmonary valve atresia IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0011060 abnormal kinocilium morphology IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0011707 impaired fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0011865 abnormal podocyte motility IAGP N RGD:5509061 20141003 MGI PMID:24302887 1319875 Wdpcp WD repeat containing planar cell polarity effector gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:24302887 1319878 Itm2c integral membrane protein 2C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:30042348 1319878 Itm2c integral membrane protein 2C gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1319878 Itm2c integral membrane protein 2C gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20201022 MGI 1319878 Itm2c integral membrane protein 2C gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1319885 Reep6 receptor accessory protein 6 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20180809 MGI PMID:28475715 1319885 Reep6 receptor accessory protein 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20201022 MGI PMID:32101290 1319885 Reep6 receptor accessory protein 6 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20201022 MGI PMID:32101290 1319885 Reep6 receptor accessory protein 6 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20201022 MGI PMID:32101290 1319885 Reep6 receptor accessory protein 6 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20180809 MGI PMID:27889058 1319885 Reep6 receptor accessory protein 6 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20180809 MGI PMID:27889058 1319885 Reep6 receptor accessory protein 6 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20180809 MGI PMID:27889058 1319885 Reep6 receptor accessory protein 6 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20201022 MGI PMID:32101290 1319885 Reep6 receptor accessory protein 6 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20201022 MGI PMID:32101290 1319885 Reep6 receptor accessory protein 6 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20180809 MGI PMID:27889058 1319885 Reep6 receptor accessory protein 6 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20180809 MGI PMID:28475715 1319885 Reep6 receptor accessory protein 6 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20180809 MGI PMID:28475715 1319885 Reep6 receptor accessory protein 6 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20180809 MGI PMID:27889058 1319885 Reep6 receptor accessory protein 6 gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20180809 MGI PMID:27889058 1319885 Reep6 receptor accessory protein 6 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20180809 MGI PMID:27889058 1319885 Reep6 receptor accessory protein 6 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20180809 MGI PMID:28475715 1319885 Reep6 receptor accessory protein 6 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20180809 MGI PMID:28475715 1319885 Reep6 receptor accessory protein 6 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20180809 MGI PMID:27889058 1319885 Reep6 receptor accessory protein 6 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20180809 MGI PMID:28475715 1319885 Reep6 receptor accessory protein 6 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20180809 MGI PMID:27889058 1319885 Reep6 receptor accessory protein 6 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20180809 MGI PMID:28475715 1319885 Reep6 receptor accessory protein 6 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20180809 MGI PMID:28475715 1319885 Reep6 receptor accessory protein 6 gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20180809 MGI PMID:28475715 1319888 Gprc5b G protein-coupled receptor, family C, group 5, member B gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20181227 MGI 1319888 Gprc5b G protein-coupled receptor, family C, group 5, member B gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21840300 1319888 Gprc5b G protein-coupled receptor, family C, group 5, member B gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170105 MGI 1319888 Gprc5b G protein-coupled receptor, family C, group 5, member B gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:21840300 1319888 Gprc5b G protein-coupled receptor, family C, group 5, member B gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20170105 MGI 1319888 Gprc5b G protein-coupled receptor, family C, group 5, member B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21840300 1319888 Gprc5b G protein-coupled receptor, family C, group 5, member B gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21840300 1319892 Crip3 cysteine-rich protein 3 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:11713292 1319892 Crip3 cysteine-rich protein 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11713292 1319892 Crip3 cysteine-rich protein 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1319892 Crip3 cysteine-rich protein 3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11713292 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20180712 MGI PMID:23580486 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17065522 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20180712 MGI PMID:23580486 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0002183 gliosis IAGP N RGD:5509061 20180712 MGI PMID:23580486 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17065522 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:17065522 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20190131 MGI PMID:19815523 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17065522 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20190131 MGI PMID:19815523 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20180712 MGI PMID:23580486 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20190314 MGI PMID:19815523 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20180712 MGI PMID:23580486 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20180712 MGI PMID:23580486 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0006075 abnormal retina cone bipolar cell morphology IAGP N RGD:5509061 20180712 MGI PMID:23580486 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20180712 MGI PMID:23580486 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20180712 MGI PMID:23580486 1319894 Gnat2 G protein subunit alpha transducin 2 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20180712 MGI PMID:23580486 1319896 Rad17 RAD17 checkpoint clamp loader component gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15297881 1319896 Rad17 RAD17 checkpoint clamp loader component gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:15297881 1319896 Rad17 RAD17 checkpoint clamp loader component gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:15297881 1319896 Rad17 RAD17 checkpoint clamp loader component gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15297881 1319896 Rad17 RAD17 checkpoint clamp loader component gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15297881 1319896 Rad17 RAD17 checkpoint clamp loader component gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15297881 1319896 Rad17 RAD17 checkpoint clamp loader component gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15297881 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:21038445 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:21038445 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15728677 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:21769484 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:15728677 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:21769484 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:21769484 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15728677 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:21038445 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:15728677 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:21769484 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:21038445 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15728677 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0003932 abnormal molar crown morphology IAGP N RGD:5509061 20141003 MGI PMID:21038445 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15728677 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21769484 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0005206 abnormal aqueous humor IAGP N RGD:5509061 20141003 MGI PMID:21769484 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21038445 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0014165 absent ciliary process IAGP N RGD:5509061 20160414 MGI PMID:15728677 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0014175 abnormal ciliary epithelium morphology IAGP N RGD:5509061 20160505 MGI PMID:15728677 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:21038445 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0030138 abnormal lower incisor color IAGP N RGD:5509061 20171005 MGI PMID:21038445 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0030500 conical molar IAGP N RGD:5509061 20180118 MGI PMID:21038445 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0030522 abnormal stellate reticulum morphology IAGP N RGD:5509061 20180118 MGI PMID:21038445 1319898 Nectin3 nectin cell adhesion molecule 3 gene MP:0030523 abnormal stratum intermedium morphology IAGP N RGD:5509061 20180118 MGI PMID:21038445 1319907 Cdk18 cyclin dependent kinase 18 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:22972987 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12556483 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0002491 decreased IgD level IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22972987 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:12556483 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12556483 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23509369 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12556483 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12556483 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12627171 1319912 Tab2 TGF-beta activated kinase 1/MAP3K7 binding protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22972987 1319916 Cisd1 CDGSH iron sulfur domain 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1319916 Cisd1 CDGSH iron sulfur domain 1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20221215 MGI 1319916 Cisd1 CDGSH iron sulfur domain 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:17376863 1319920 Maff v-maf musculoaponeurotic fibrosarcoma oncogene family, protein F (avian) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10409670 1319924 4931406C07Rik RIKEN cDNA 4931406C07 gene gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20211021 MGI 1319924 4931406C07Rik RIKEN cDNA 4931406C07 gene gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20211021 MGI 1319924 4931406C07Rik RIKEN cDNA 4931406C07 gene gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 1319929 Kat14 lysine acetyltransferase 14 gene MP:0000161 scoliosis IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0001258 decreased body length IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1319929 Kat14 lysine acetyltransferase 14 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:20808945 1319929 Kat14 lysine acetyltransferase 14 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20160804 MGI 1319929 Kat14 lysine acetyltransferase 14 gene MP:0001324 abnormal eye pigmentation IEA N RGD:5509061 20160804 MGI 1319929 Kat14 lysine acetyltransferase 14 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19103755 1319929 Kat14 lysine acetyltransferase 14 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20160804 MGI 1319929 Kat14 lysine acetyltransferase 14 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0002697 abnormal eye size IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0002700 increased opacity of vitreous body IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20160804 MGI 1319929 Kat14 lysine acetyltransferase 14 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:19103755 1319929 Kat14 lysine acetyltransferase 14 gene MP:0003671 abnormal eyelid aperture IEA N RGD:5509061 20160804 MGI 1319929 Kat14 lysine acetyltransferase 14 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1319929 Kat14 lysine acetyltransferase 14 gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19103755 1319929 Kat14 lysine acetyltransferase 14 gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20160804 MGI 1319929 Kat14 lysine acetyltransferase 14 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160804 MGI 1319929 Kat14 lysine acetyltransferase 14 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20160922 MGI PMID:24652767 1319929 Kat14 lysine acetyltransferase 14 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19103755 1319929 Kat14 lysine acetyltransferase 14 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20171116 MGI PMID:27310661 1319929 Kat14 lysine acetyltransferase 14 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20808945 1319929 Kat14 lysine acetyltransferase 14 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19103755 1319935 Insm1 insulinoma-associated 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:16951258 1319935 Insm1 insulinoma-associated 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:16951258 1319935 Insm1 insulinoma-associated 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21284846 1319935 Insm1 insulinoma-associated 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:16951258 1319935 Insm1 insulinoma-associated 1 gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141003 MGI PMID:24227653 1319935 Insm1 insulinoma-associated 1 gene MP:0003972 decreased pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:24227653 1319935 Insm1 insulinoma-associated 1 gene MP:0004141 abnormal enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16951258 1319935 Insm1 insulinoma-associated 1 gene MP:0005128 decreased adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:24227653 1319935 Insm1 insulinoma-associated 1 gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:24227653 1319935 Insm1 insulinoma-associated 1 gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:24227653 1319935 Insm1 insulinoma-associated 1 gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:24227653 1319935 Insm1 insulinoma-associated 1 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:24227653 1319935 Insm1 insulinoma-associated 1 gene MP:0005138 decreased prolactin level IAGP N RGD:5509061 20141003 MGI PMID:24227653 1319935 Insm1 insulinoma-associated 1 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:24227653 1319935 Insm1 insulinoma-associated 1 gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20141120 MGI PMID:25053427 1319935 Insm1 insulinoma-associated 1 gene MP:0008330 absent somatotrophs IAGP N RGD:5509061 20141003 MGI PMID:24227653 1319935 Insm1 insulinoma-associated 1 gene MP:0008339 absent thyrotrophs IAGP N RGD:5509061 20141003 MGI PMID:24227653 1319935 Insm1 insulinoma-associated 1 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21284846 1319935 Insm1 insulinoma-associated 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21284846 1319935 Insm1 insulinoma-associated 1 gene MP:0009165 abnormal endocrine pancreas morphology IAGP N RGD:5509061 20141120 MGI PMID:25053427 1319935 Insm1 insulinoma-associated 1 gene MP:0009169 pancreatic islet hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16951258 1319935 Insm1 insulinoma-associated 1 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:16951258 1319935 Insm1 insulinoma-associated 1 gene MP:0009181 decreased pancreatic delta cell number IAGP N RGD:5509061 20141003 MGI PMID:16951258 1319935 Insm1 insulinoma-associated 1 gene MP:0009185 increased PP cell number IAGP N RGD:5509061 20141003 MGI PMID:16951258 1319935 Insm1 insulinoma-associated 1 gene MP:0009187 absent PP cells IAGP N RGD:5509061 20141003 MGI PMID:16951258 1319935 Insm1 insulinoma-associated 1 gene MP:0009191 decreased pancreatic epsilon cell number IAGP N RGD:5509061 20141003 MGI PMID:16951258 1319935 Insm1 insulinoma-associated 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21284846 1319935 Insm1 insulinoma-associated 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16951258 1319935 Insm1 insulinoma-associated 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16951258 1319935 Insm1 insulinoma-associated 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21284846 1319935 Insm1 insulinoma-associated 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21284846 1319935 Insm1 insulinoma-associated 1 gene MP:0011400 lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 1319935 Insm1 insulinoma-associated 1 gene MP:0011910 decreased pancreatic endocrine progenitor cell proliferation IAGP N RGD:5509061 20141120 MGI PMID:25053427 1319935 Insm1 insulinoma-associated 1 gene MP:0011911 abnormal pancreatic endocrine progenitor cell physiology IAGP N RGD:5509061 20141120 MGI PMID:25053427 1319935 Insm1 insulinoma-associated 1 gene MP:0011932 abnormal endocrine pancreas development IAGP N RGD:5509061 20141003 MGI PMID:16951258 1319935 Insm1 insulinoma-associated 1 gene MP:0011932 abnormal endocrine pancreas development IAGP N RGD:5509061 20141120 MGI PMID:25053427 1319935 Insm1 insulinoma-associated 1 gene MP:0013220 increased pancreas apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16951258 1319937 Ppp1r18 protein phosphatase 1, regulatory subunit 18 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20221215 MGI PMID:35766979 1319937 Ppp1r18 protein phosphatase 1, regulatory subunit 18 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20221215 MGI PMID:35766979 1319937 Ppp1r18 protein phosphatase 1, regulatory subunit 18 gene MP:0000692 small spleen IAGP N RGD:5509061 20221215 MGI PMID:35766979 1319937 Ppp1r18 protein phosphatase 1, regulatory subunit 18 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20221215 MGI PMID:35766979 1319937 Ppp1r18 protein phosphatase 1, regulatory subunit 18 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20221215 MGI PMID:35766979 1319937 Ppp1r18 protein phosphatase 1, regulatory subunit 18 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20221215 MGI PMID:35766979 1319937 Ppp1r18 protein phosphatase 1, regulatory subunit 18 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20221215 MGI PMID:35766979 1319937 Ppp1r18 protein phosphatase 1, regulatory subunit 18 gene MP:0005387 immune system phenotype IAGP N RGD:5509061 20221215 MGI PMID:35766979 1319937 Ppp1r18 protein phosphatase 1, regulatory subunit 18 gene MP:0020212 impaired leukocyte migration IAGP N RGD:5509061 20221215 MGI PMID:35766979 1319941 Zmym4 zinc finger, MYM-type 4 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 1319941 Zmym4 zinc finger, MYM-type 4 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1319941 Zmym4 zinc finger, MYM-type 4 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1319941 Zmym4 zinc finger, MYM-type 4 gene MP:0003443 increased circulating glycerol level IEA N RGD:5509061 20210128 MGI 1319941 Zmym4 zinc finger, MYM-type 4 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1319941 Zmym4 zinc finger, MYM-type 4 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1319941 Zmym4 zinc finger, MYM-type 4 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1319941 Zmym4 zinc finger, MYM-type 4 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1319941 Zmym4 zinc finger, MYM-type 4 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20201022 MGI PMID:32492392 1319947 Cdyl2 chromodomain protein, Y chromosome-like 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1319947 Cdyl2 chromodomain protein, Y chromosome-like 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20200514 MGI 1319947 Cdyl2 chromodomain protein, Y chromosome-like 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1319947 Cdyl2 chromodomain protein, Y chromosome-like 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1319947 Cdyl2 chromodomain protein, Y chromosome-like 2 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20240523 MGI 1319951 Setd3 SET domain containing 3 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 1319951 Setd3 SET domain containing 3 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1319951 Setd3 SET domain containing 3 gene MP:0001147 small testis IEA N RGD:5509061 20170105 MGI 1319951 Setd3 SET domain containing 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20170105 MGI 1319951 Setd3 SET domain containing 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1319951 Setd3 SET domain containing 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20190516 MGI PMID:30626964 1319951 Setd3 SET domain containing 3 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20170105 MGI 1319951 Setd3 SET domain containing 3 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20170105 MGI 1319951 Setd3 SET domain containing 3 gene MP:0002764 short tibia IEA N RGD:5509061 20170105 MGI 1319951 Setd3 SET domain containing 3 gene MP:0003900 shortened QT interval IEA N RGD:5509061 20220519 MGI 1319951 Setd3 SET domain containing 3 gene MP:0004514 dystocia IAGP N RGD:5509061 20190516 MGI PMID:30626964 1319951 Setd3 SET domain containing 3 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20201231 MGI 1319951 Setd3 SET domain containing 3 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 1319951 Setd3 SET domain containing 3 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20190516 MGI PMID:30626964 1319951 Setd3 SET domain containing 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20170105 MGI 1319951 Setd3 SET domain containing 3 gene MP:0009709 hydrometra IEA N RGD:5509061 20170105 MGI 1319951 Setd3 SET domain containing 3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1319951 Setd3 SET domain containing 3 gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20190516 MGI PMID:30626964 1319951 Setd3 SET domain containing 3 gene MP:0020422 decreased freezing behavior IEA N RGD:5509061 20231207 MGI 1319951 Setd3 SET domain containing 3 gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20200917 MGI PMID:31527793 1319953 Nol8 nucleolar protein 8 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20200402 MGI 1319953 Nol8 nucleolar protein 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319953 Nol8 nucleolar protein 8 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1319956 Gga3 golgi associated, gamma adaptin ear containing, ARF binding protein 3 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:22291915 1319956 Gga3 golgi associated, gamma adaptin ear containing, ARF binding protein 3 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:22291915 1319956 Gga3 golgi associated, gamma adaptin ear containing, ARF binding protein 3 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:22291915 1319956 Gga3 golgi associated, gamma adaptin ear containing, ARF binding protein 3 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:22291915 1319956 Gga3 golgi associated, gamma adaptin ear containing, ARF binding protein 3 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:22291915 1319956 Gga3 golgi associated, gamma adaptin ear containing, ARF binding protein 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22291915 1319956 Gga3 golgi associated, gamma adaptin ear containing, ARF binding protein 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22291915 1319958 Lrig2 leucine-rich repeats and immunoglobulin-like domains 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:24086156 1319958 Lrig2 leucine-rich repeats and immunoglobulin-like domains 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24023893 1319958 Lrig2 leucine-rich repeats and immunoglobulin-like domains 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24023893 1319958 Lrig2 leucine-rich repeats and immunoglobulin-like domains 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24086156 1319958 Lrig2 leucine-rich repeats and immunoglobulin-like domains 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:24086156 1319958 Lrig2 leucine-rich repeats and immunoglobulin-like domains 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:24023893 1319958 Lrig2 leucine-rich repeats and immunoglobulin-like domains 2 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:24023893 1319958 Lrig2 leucine-rich repeats and immunoglobulin-like domains 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:24023893 1319958 Lrig2 leucine-rich repeats and immunoglobulin-like domains 2 gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:24023893 1319958 Lrig2 leucine-rich repeats and immunoglobulin-like domains 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24023893 1319958 Lrig2 leucine-rich repeats and immunoglobulin-like domains 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24086156 1319958 Lrig2 leucine-rich repeats and immunoglobulin-like domains 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:24023893 1319958 Lrig2 leucine-rich repeats and immunoglobulin-like domains 2 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:24086156 1319958 Lrig2 leucine-rich repeats and immunoglobulin-like domains 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:24086156 1319958 Lrig2 leucine-rich repeats and immunoglobulin-like domains 2 gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:24086156 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191205 MGI 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0003087 absent allantois IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0012724 absent head fold IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191205 MGI 1319961 Mrpl44 mitochondrial ribosomal protein L44 gene MP:0014246 decreased cellular ATP level IAGP N RGD:5509061 20241024 MGI PMID:32376682 1319964 B3galt6 UDP-Gal:betaGal beta 1,3-galactosyltransferase, polypeptide 6 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1319964 B3galt6 UDP-Gal:betaGal beta 1,3-galactosyltransferase, polypeptide 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1319964 B3galt6 UDP-Gal:betaGal beta 1,3-galactosyltransferase, polypeptide 6 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1319964 B3galt6 UDP-Gal:betaGal beta 1,3-galactosyltransferase, polypeptide 6 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19479052 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19479052 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19479052 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:19479052 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19479052 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20160707 MGI PMID:22508039 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:19479052 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:22733973 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22733973 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:22733973 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:19479052 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:22733973 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:19479052 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:19479052 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:19479052 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22733973 1319966 Gpr68 G protein-coupled receptor 68 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:19479052 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20190124 MGI PMID:25340873 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20190124 MGI PMID:25340873 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21404367 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0002758 long tail IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0003849 greasy coat IAGP N RGD:5509061 20190124 MGI PMID:25340873 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0008933 abnormal motile primary cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20160804 MGI 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0010866 abnormal prenatal body size IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18296642 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20190124 MGI PMID:25340873 1319968 Vangl1 VANGL planar cell polarity 1 gene MP:0012027 abnormal embryonic cilium location or orientation IAGP N RGD:5509061 20141003 MGI PMID:20562861 1319969 Rnf145 ring finger protein 145 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1319973 Pbk PDZ binding kinase gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:21715333 1319973 Pbk PDZ binding kinase gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:21715333 1319973 Pbk PDZ binding kinase gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:21715333 1319973 Pbk PDZ binding kinase gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20211021 MGI PMID:32586419 1319973 Pbk PDZ binding kinase gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21715333 1319973 Pbk PDZ binding kinase gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21715333 1319973 Pbk PDZ binding kinase gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21715333 1319973 Pbk PDZ binding kinase gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21715333 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0001260 increased body weight IAGP N RGD:5509061 20220721 MGI PMID:33692754 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20220721 MGI PMID:33692754 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20220721 MGI PMID:33692754 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20220721 MGI PMID:33692754 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0001513 limb grasping IAGP N RGD:5509061 20220721 MGI PMID:33692754 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0002764 short tibia IEA N RGD:5509061 20240523 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20220721 MGI PMID:33692754 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20220721 MGI PMID:33692754 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20220721 MGI PMID:33692754 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0005356 positive geotaxis IAGP N RGD:5509061 20220721 MGI PMID:33692754 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20220721 MGI PMID:33692754 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20220721 MGI PMID:33692754 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20220721 MGI PMID:33692754 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0011625 cystolithiasis IEA N RGD:5509061 20230601 MGI 1319975 Plppr5 phospholipid phosphatase related 5 gene MP:0020870 decreased thigmotaxis IAGP N RGD:5509061 20220721 MGI PMID:33692754 1319976 Akirin1 akirin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18066067 1319980 G3bp2 G3BP stress granule assembly factor 2 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20220915 MGI PMID:35782098 1319980 G3bp2 G3BP stress granule assembly factor 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319980 G3bp2 G3BP stress granule assembly factor 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220915 MGI PMID:35782098 1319982 Aurkc aurora kinase C gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17192404 1319982 Aurkc aurora kinase C gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17192404 1319982 Aurkc aurora kinase C gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:17192404 1319982 Aurkc aurora kinase C gene MP:0009231 detached acrosome IAGP N RGD:5509061 20141003 MGI PMID:17192404 1319982 Aurkc aurora kinase C gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:17192404 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:16054034 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21982646 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:16054034 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:18682239 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:18682239 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16054034 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19543268 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19543268 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:19543268 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:16054034 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:16054034 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0003558 absent uterus IAGP N RGD:5509061 20141003 MGI PMID:16054034 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0003576 oviduct hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16054034 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:19543268 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0003826 abnormal Mullerian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16054034 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:16054034 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16054034 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:16054034 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:11353389 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:15329828 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:16054034 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:3491125 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:7601909 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:16054034 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0009072 absent cranial vagina IAGP N RGD:5509061 20141003 MGI PMID:16054034 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0009073 absent Wolffian ducts IAGP N RGD:5509061 20141003 MGI PMID:16054034 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19543268 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:19543268 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0011843 abnormal kidney collecting duct epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19543268 1319984 Wnt9b wingless-type MMTV integration site family, member 9B gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:21982646 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21807889 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20190912 MGI PMID:27311593 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20190912 MGI PMID:27311593 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0000603 pale liver IAGP N RGD:5509061 20190912 MGI PMID:27311593 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20190912 MGI PMID:27311593 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20190912 MGI PMID:27311593 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190912 MGI PMID:27311593 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20190912 MGI PMID:27311593 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21807889 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20190912 MGI PMID:27311593 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21807889 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21807889 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20190912 MGI PMID:27311593 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20190912 MGI PMID:27311593 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20190912 MGI PMID:27311593 1319986 Mia2 MIA SH3 domain ER export factor 2 gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20190912 MGI PMID:27311593 1319992 Dtnb dystrobrevin, beta gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16540561 1319992 Dtnb dystrobrevin, beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11585924 1319992 Dtnb dystrobrevin, beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16540561 1319992 Dtnb dystrobrevin, beta gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:16540561 1319992 Dtnb dystrobrevin, beta gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16540561 1319998 Tfeb transcription factor EB gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11930005 1319998 Tfeb transcription factor EB gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1319998 Tfeb transcription factor EB gene MP:0001512 trunk curl IEA N RGD:5509061 20190502 MGI 1319998 Tfeb transcription factor EB gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:11930005 1319998 Tfeb transcription factor EB gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11930005 1319998 Tfeb transcription factor EB gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11930005 1319998 Tfeb transcription factor EB gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9626501 1319998 Tfeb transcription factor EB gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1319998 Tfeb transcription factor EB gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1319998 Tfeb transcription factor EB gene MP:0003960 increased lean body mass IEA N RGD:5509061 20190502 MGI 1319998 Tfeb transcription factor EB gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20190502 MGI 1319998 Tfeb transcription factor EB gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11930005 1319998 Tfeb transcription factor EB gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20240125 MGI PMID:35662396 1319998 Tfeb transcription factor EB gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1319998 Tfeb transcription factor EB gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1319998 Tfeb transcription factor EB gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1320000 Irak2 interleukin-1 receptor-associated kinase 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18438411 1320000 Irak2 interleukin-1 receptor-associated kinase 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18438411 1320000 Irak2 interleukin-1 receptor-associated kinase 2 gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 1320000 Irak2 interleukin-1 receptor-associated kinase 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1320000 Irak2 interleukin-1 receptor-associated kinase 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19224918 1320000 Irak2 interleukin-1 receptor-associated kinase 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19224918 1320000 Irak2 interleukin-1 receptor-associated kinase 2 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:23918981 1320000 Irak2 interleukin-1 receptor-associated kinase 2 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:19224918 1320000 Irak2 interleukin-1 receptor-associated kinase 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:19224918 1320000 Irak2 interleukin-1 receptor-associated kinase 2 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:19224918 1320000 Irak2 interleukin-1 receptor-associated kinase 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:18438411 1320000 Irak2 interleukin-1 receptor-associated kinase 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:19224918 1320000 Irak2 interleukin-1 receptor-associated kinase 2 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19224918 1320000 Irak2 interleukin-1 receptor-associated kinase 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1320002 D1Pas1 DNA segment, Chr 1, Pasteur Institute 1 gene MP:0001147 small testis IEA N RGD:5509061 20161201 MGI 1320002 D1Pas1 DNA segment, Chr 1, Pasteur Institute 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1320006 Sprr3 small proline-rich protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160630 MGI PMID:25278290 1320006 Sprr3 small proline-rich protein 3 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1320006 Sprr3 small proline-rich protein 3 gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20160630 MGI PMID:25278290 1320006 Sprr3 small proline-rich protein 3 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20160630 MGI PMID:25278290 1320006 Sprr3 small proline-rich protein 3 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20160630 MGI PMID:25278290 1320006 Sprr3 small proline-rich protein 3 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20160630 MGI PMID:25278290 1320006 Sprr3 small proline-rich protein 3 gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20211021 MGI 1320011 Aopep aminopeptidase O gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20200514 MGI 1320011 Aopep aminopeptidase O gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17803194 1320011 Aopep aminopeptidase O gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1320011 Aopep aminopeptidase O gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20221215 MGI 1320011 Aopep aminopeptidase O gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1320013 Dlx1 distal-less homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:9187081 1320013 Dlx1 distal-less homeobox 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1320013 Dlx1 distal-less homeobox 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20171026 MGI PMID:18697905 1320013 Dlx1 distal-less homeobox 1 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9187081 1320013 Dlx1 distal-less homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9187081 1320013 Dlx1 distal-less homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9187081 1320013 Dlx1 distal-less homeobox 1 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1320013 Dlx1 distal-less homeobox 1 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20171005 MGI PMID:18697905 1320013 Dlx1 distal-less homeobox 1 gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1320013 Dlx1 distal-less homeobox 1 gene MP:0004666 absent stapedial artery IAGP N RGD:5509061 20141003 MGI PMID:9187081 1320013 Dlx1 distal-less homeobox 1 gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20141003 MGI PMID:16632068 1320013 Dlx1 distal-less homeobox 1 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:9187081 1320013 Dlx1 distal-less homeobox 1 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1320013 Dlx1 distal-less homeobox 1 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:18697905 1320013 Dlx1 distal-less homeobox 1 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1320013 Dlx1 distal-less homeobox 1 gene MP:0009917 abnormal hyoid bone body morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1320013 Dlx1 distal-less homeobox 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20151224 MGI PMID:24507192 1320013 Dlx1 distal-less homeobox 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20151224 MGI PMID:24507192 1320013 Dlx1 distal-less homeobox 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16632068 1320013 Dlx1 distal-less homeobox 1 gene MP:0030127 small stapes IAGP N RGD:5509061 20170928 MGI PMID:9187081 1320013 Dlx1 distal-less homeobox 1 gene MP:0030406 absent stapes obturator foramen IAGP N RGD:5509061 20171207 MGI PMID:9187081 1320017 Taf15 TATA-box binding protein associated factor 15 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1320017 Taf15 TATA-box binding protein associated factor 15 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1320017 Taf15 TATA-box binding protein associated factor 15 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 1320017 Taf15 TATA-box binding protein associated factor 15 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1320018 Trex1 three prime repair exonuclease 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15254239 1320018 Trex1 three prime repair exonuclease 1 gene MP:0000376 folliculitis IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15254239 1320018 Trex1 three prime repair exonuclease 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20230105 MGI PMID:36217001 1320018 Trex1 three prime repair exonuclease 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15254239 1320018 Trex1 three prime repair exonuclease 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15254239 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20171207 MGI PMID:28351661 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20171207 MGI PMID:28351661 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230105 MGI PMID:36217001 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230105 MGI PMID:36217001 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:15254239 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20160915 MGI PMID:27496731 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:23972988 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20160915 MGI PMID:27496731 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:15254239 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:15254239 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20160915 MGI PMID:27496731 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20160915 MGI PMID:27496731 1320018 Trex1 three prime repair exonuclease 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15254239 1320018 Trex1 three prime repair exonuclease 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23972988 1320018 Trex1 three prime repair exonuclease 1 gene MP:0002083 premature death IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0002083 premature death IAGP N RGD:5509061 20160915 MGI PMID:27496731 1320018 Trex1 three prime repair exonuclease 1 gene MP:0002083 premature death IAGP N RGD:5509061 20230105 MGI PMID:36217001 1320018 Trex1 three prime repair exonuclease 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15254239 1320018 Trex1 three prime repair exonuclease 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0002704 tubular nephritis IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:23972988 1320018 Trex1 three prime repair exonuclease 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20160915 MGI PMID:27496731 1320018 Trex1 three prime repair exonuclease 1 gene MP:0003946 renal necrosis IAGP N RGD:5509061 20141003 MGI PMID:15254239 1320018 Trex1 three prime repair exonuclease 1 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0004510 myositis IAGP N RGD:5509061 20160915 MGI PMID:27496731 1320018 Trex1 three prime repair exonuclease 1 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:15254239 1320018 Trex1 three prime repair exonuclease 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:22284419 1320018 Trex1 three prime repair exonuclease 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:23972988 1320018 Trex1 three prime repair exonuclease 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20230105 MGI PMID:36217001 1320018 Trex1 three prime repair exonuclease 1 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15254239 1320018 Trex1 three prime repair exonuclease 1 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20171207 MGI PMID:28351661 1320018 Trex1 three prime repair exonuclease 1 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20230105 MGI PMID:36217001 1320018 Trex1 three prime repair exonuclease 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20230105 MGI PMID:36217001 1320018 Trex1 three prime repair exonuclease 1 gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20160908 MGI PMID:27496731 1320018 Trex1 three prime repair exonuclease 1 gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20160804 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0014347 increased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:15254239 1320018 Trex1 three prime repair exonuclease 1 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:25848017 1320018 Trex1 three prime repair exonuclease 1 gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:27496731 1320018 Trex1 three prime repair exonuclease 1 gene MP:0031054 bronchiolitis IAGP N RGD:5509061 20200618 MGI PMID:25848017 1320020 Adam8 a disintegrin and metallopeptidase domain 8 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1320020 Adam8 a disintegrin and metallopeptidase domain 8 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1320020 Adam8 a disintegrin and metallopeptidase domain 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15580619 1320020 Adam8 a disintegrin and metallopeptidase domain 8 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:19737139 1320020 Adam8 a disintegrin and metallopeptidase domain 8 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:20683884 1320020 Adam8 a disintegrin and metallopeptidase domain 8 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:20683884 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210422 MGI 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210422 MGI 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210422 MGI 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0000745 tremors IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20210422 MGI 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20210422 MGI 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180222 MGI PMID:28123425 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210422 MGI 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20180222 MGI PMID:28123425 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0012051 spasticity IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20221103 MGI 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 1320022 Ankfy1 ankyrin repeat and FYVE domain containing 1 gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20190718 MGI PMID:28588446 1320027 Lrrc8d leucine rich repeat containing 8D gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1320027 Lrrc8d leucine rich repeat containing 8D gene MP:0005387 immune system phenotype IAGP N RGD:5509061 20201001 MGI PMID:32277911 1320031 Crygs crystallin, gamma S gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:11121426 1320031 Crygs crystallin, gamma S gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:22715935 1320031 Crygs crystallin, gamma S gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:11121426 1320031 Crygs crystallin, gamma S gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:12079281 1320031 Crygs crystallin, gamma S gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:19224648 1320031 Crygs crystallin, gamma S gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:8812411 1320031 Crygs crystallin, gamma S gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1320031 Crygs crystallin, gamma S gene MP:0002579 disorganized secondary lens fibers IAGP N RGD:5509061 20141003 MGI PMID:6877261 1320031 Crygs crystallin, gamma S gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11121426 1320031 Crygs crystallin, gamma S gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22715935 1320031 Crygs crystallin, gamma S gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:8812411 1320031 Crygs crystallin, gamma S gene MP:0010263 total cataract IAGP N RGD:5509061 20141003 MGI PMID:11121426 1320031 Crygs crystallin, gamma S gene MP:0010263 total cataract IAGP N RGD:5509061 20141003 MGI PMID:8812411 1320035 Nnmt nicotinamide N-methyltransferase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1320035 Nnmt nicotinamide N-methyltransferase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1320035 Nnmt nicotinamide N-methyltransferase gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1320035 Nnmt nicotinamide N-methyltransferase gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 1320035 Nnmt nicotinamide N-methyltransferase gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210128 MGI 1320035 Nnmt nicotinamide N-methyltransferase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1320035 Nnmt nicotinamide N-methyltransferase gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210128 MGI 1320035 Nnmt nicotinamide N-methyltransferase gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1320037 Emilin3 elastin microfibril interfacer 3 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 1320037 Emilin3 elastin microfibril interfacer 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1320037 Emilin3 elastin microfibril interfacer 3 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220811 MGI 1320037 Emilin3 elastin microfibril interfacer 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1320040 Dapl1 death associated protein-like 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1320040 Dapl1 death associated protein-like 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20191128 MGI PMID:28334846 1320040 Dapl1 death associated protein-like 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1320040 Dapl1 death associated protein-like 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1320040 Dapl1 death associated protein-like 1 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20231207 MGI 1320040 Dapl1 death associated protein-like 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20240523 MGI 1320040 Dapl1 death associated protein-like 1 gene MP:0005549 retina pigment epithelium hyperplasia IAGP N RGD:5509061 20191128 MGI PMID:28334846 1320040 Dapl1 death associated protein-like 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 1320040 Dapl1 death associated protein-like 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20240523 MGI 1320042 Pla2g2e phospholipase A2, group IIE gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1320042 Pla2g2e phospholipase A2, group IIE gene MP:0011951 increased cardiac stroke volume IEA N RGD:5509061 20211021 MGI 1320048 Dtymk deoxythymidylate kinase gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20240523 MGI PMID:38621447 1320048 Dtymk deoxythymidylate kinase gene MP:0014257 embryonic lethality prior to tooth bud stage, complete penetrance IAGP N RGD:5509061 20240523 MGI PMID:38621447 1320054 Atp8a1 ATPase phospholipid transporting 8A1 gene MP:0001260 increased body weight IEA N RGD:5509061 20141003 MGI 1320054 Atp8a1 ATPase phospholipid transporting 8A1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1320054 Atp8a1 ATPase phospholipid transporting 8A1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20141003 MGI 1320054 Atp8a1 ATPase phospholipid transporting 8A1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20160804 MGI 1320054 Atp8a1 ATPase phospholipid transporting 8A1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20141003 MGI 1320056 Ank1 ankyrin 1, erythroid gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0000314 schistocytosis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20111116 MGI 1320056 Ank1 ankyrin 1, erythroid gene MP:0000704 abnormal thymus development IEA N RGD:5509061 20111116 MGI 1320056 Ank1 ankyrin 1, erythroid gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:1716634 1320056 Ank1 ankyrin 1, erythroid gene MP:0000751 myopathy IAGP N RGD:5509061 20151203 MGI PMID:25354526 1320056 Ank1 ankyrin 1, erythroid gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:1716634 1320056 Ank1 ankyrin 1, erythroid gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:1716634 1320056 Ank1 ankyrin 1, erythroid gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0002095 abnormal skin pigmentation IEA N RGD:5509061 20111116 MGI 1320056 Ank1 ankyrin 1, erythroid gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20151203 MGI PMID:25354526 1320056 Ank1 ankyrin 1, erythroid gene MP:0002397 abnormal bone marrow morphology IEA N RGD:5509061 20111116 MGI 1320056 Ank1 ankyrin 1, erythroid gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10772878 1320056 Ank1 ankyrin 1, erythroid gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:1832936 1320056 Ank1 ankyrin 1, erythroid gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:6234993 1320056 Ank1 ankyrin 1, erythroid gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9236006 1320056 Ank1 ankyrin 1, erythroid gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:1391963 1320056 Ank1 ankyrin 1, erythroid gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:1391963 1320056 Ank1 ankyrin 1, erythroid gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:9236006 1320056 Ank1 ankyrin 1, erythroid gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:1832936 1320056 Ank1 ankyrin 1, erythroid gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:1832936 1320056 Ank1 ankyrin 1, erythroid gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:1832936 1320056 Ank1 ankyrin 1, erythroid gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:1391963 1320056 Ank1 ankyrin 1, erythroid gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:1391963 1320056 Ank1 ankyrin 1, erythroid gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:10772878 1320056 Ank1 ankyrin 1, erythroid gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:1832936 1320056 Ank1 ankyrin 1, erythroid gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0002814 hyperchromasia IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0002830 gallstones IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0002830 gallstones IAGP N RGD:5509061 20141003 MGI PMID:7410545 1320056 Ank1 ankyrin 1, erythroid gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20151203 MGI PMID:25354526 1320056 Ank1 ankyrin 1, erythroid gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0003332 liver abscess IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:7492791 1320056 Ank1 ankyrin 1, erythroid gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20151203 MGI PMID:25354526 1320056 Ank1 ankyrin 1, erythroid gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20151203 MGI PMID:25354526 1320056 Ank1 ankyrin 1, erythroid gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20151203 MGI PMID:25354526 1320056 Ank1 ankyrin 1, erythroid gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20151203 MGI PMID:25354526 1320056 Ank1 ankyrin 1, erythroid gene MP:0004246 abnormal extensor digitorum longus morphology IAGP N RGD:5509061 20151203 MGI PMID:25354526 1320056 Ank1 ankyrin 1, erythroid gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:1832936 1320056 Ank1 ankyrin 1, erythroid gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0005096 erythroblastosis IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:1391963 1320056 Ank1 ankyrin 1, erythroid gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20141003 MGI PMID:1391963 1320056 Ank1 ankyrin 1, erythroid gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0008387 hypochromic anemia IEA N RGD:5509061 20111116 MGI 1320056 Ank1 ankyrin 1, erythroid gene MP:0008742 abnormal kidney iron level IAGP N RGD:5509061 20141003 MGI PMID:1391963 1320056 Ank1 ankyrin 1, erythroid gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:1391963 1320056 Ank1 ankyrin 1, erythroid gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0008850 increased hemoglobin concentration distribution width IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0008956 decreased cellular hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0009411 abnormal skeletal muscle fiber triad morphology IAGP N RGD:5509061 20151203 MGI PMID:25354526 1320056 Ank1 ankyrin 1, erythroid gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20151203 MGI PMID:25354526 1320056 Ank1 ankyrin 1, erythroid gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0010035 increased erythrocyte clearance IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0010074 stomatocytosis IAGP N RGD:5509061 20141003 MGI PMID:1832936 1320056 Ank1 ankyrin 1, erythroid gene MP:0010074 stomatocytosis IAGP N RGD:5509061 20141003 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0010163 hemolysis IAGP N RGD:5509061 20141003 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0010163 hemolysis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0010177 acanthocytosis IAGP N RGD:5509061 20141003 MGI PMID:1832936 1320056 Ank1 ankyrin 1, erythroid gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0010751 decreased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6763106 1320056 Ank1 ankyrin 1, erythroid gene MP:0011188 increased erythrocyte protoporphyrin level IAGP N RGD:5509061 20141003 MGI PMID:658175 1320056 Ank1 ankyrin 1, erythroid gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:23390527 1320056 Ank1 ankyrin 1, erythroid gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20151203 MGI PMID:25354526 1320056 Ank1 ankyrin 1, erythroid gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20161124 MGI PMID:10772878 1320056 Ank1 ankyrin 1, erythroid gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:19179303 1320056 Ank1 ankyrin 1, erythroid gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:21193012 1320056 Ank1 ankyrin 1, erythroid gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:22723917 1320056 Ank1 ankyrin 1, erythroid gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:23934996 1320056 Ank1 ankyrin 1, erythroid gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:6763106 1320057 Resf1 retroelement silencing factor 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1320057 Resf1 retroelement silencing factor 1 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1320057 Resf1 retroelement silencing factor 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1320057 Resf1 retroelement silencing factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1320064 Cdkl2 cyclin dependent kinase like 2 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20210520 MGI 1320064 Cdkl2 cyclin dependent kinase like 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1320064 Cdkl2 cyclin dependent kinase like 2 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20211021 MGI 1320064 Cdkl2 cyclin dependent kinase like 2 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20201022 MGI 1320064 Cdkl2 cyclin dependent kinase like 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1320066 Pcbp2 poly(rC) binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170928 MGI PMID:26527618 1320066 Pcbp2 poly(rC) binding protein 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20170928 MGI PMID:26527618 1320066 Pcbp2 poly(rC) binding protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170928 MGI PMID:26527618 1320066 Pcbp2 poly(rC) binding protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170928 MGI PMID:26527618 1320066 Pcbp2 poly(rC) binding protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170928 MGI PMID:26527618 1320066 Pcbp2 poly(rC) binding protein 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20170928 MGI PMID:26527618 1320066 Pcbp2 poly(rC) binding protein 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170928 MGI PMID:26527618 1320066 Pcbp2 poly(rC) binding protein 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20170928 MGI PMID:26527618 1320066 Pcbp2 poly(rC) binding protein 2 gene MP:0011176 abnormal erythroblast morphology IAGP N RGD:5509061 20170928 MGI PMID:26527618 1320066 Pcbp2 poly(rC) binding protein 2 gene MP:0011898 abnormal platelet cell number IAGP N RGD:5509061 20170928 MGI PMID:26527618 1320066 Pcbp2 poly(rC) binding protein 2 gene MP:0013848 subcutaneous edema IAGP N RGD:5509061 20170928 MGI PMID:26527618 1320067 Taf1d TATA-box binding protein associated factor, RNA polymerase I, D gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20241010 MGI 1320067 Taf1d TATA-box binding protein associated factor, RNA polymerase I, D gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241010 MGI 1320067 Taf1d TATA-box binding protein associated factor, RNA polymerase I, D gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241017 MGI 1320067 Taf1d TATA-box binding protein associated factor, RNA polymerase I, D gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1320069 Prkcsh protein kinase C substrate 80K-H gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1320069 Prkcsh protein kinase C substrate 80K-H gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21685914 1320069 Prkcsh protein kinase C substrate 80K-H gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:21685914 1320069 Prkcsh protein kinase C substrate 80K-H gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:21685914 1320069 Prkcsh protein kinase C substrate 80K-H gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:21685914 1320069 Prkcsh protein kinase C substrate 80K-H gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:21685914 1320069 Prkcsh protein kinase C substrate 80K-H gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:21685914 1320069 Prkcsh protein kinase C substrate 80K-H gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:21685914 1320069 Prkcsh protein kinase C substrate 80K-H gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21685914 1320069 Prkcsh protein kinase C substrate 80K-H gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320069 Prkcsh protein kinase C substrate 80K-H gene MP:0011344 abnormal loop of Henle ascending limb thick segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21685914 1320069 Prkcsh protein kinase C substrate 80K-H gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20180222 MGI PMID:21685914 1320069 Prkcsh protein kinase C substrate 80K-H gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20180222 MGI PMID:21685914 1320069 Prkcsh protein kinase C substrate 80K-H gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1320071 Midn midnolin gene MP:0000111 cleft palate IEA N RGD:5509061 20111116 MGI 1320071 Midn midnolin gene MP:0001127 small ovary IEA N RGD:5509061 20111116 MGI 1320071 Midn midnolin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1320071 Midn midnolin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1320075 Kcna7 potassium voltage-gated channel, shaker-related subfamily, member 7 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220519 MGI 1320075 Kcna7 potassium voltage-gated channel, shaker-related subfamily, member 7 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220519 MGI 1320078 Fam193a family with sequence homology 193, member A gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1320081 Sorbs1 sorbin and SH3 domain containing 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17351624 1320081 Sorbs1 sorbin and SH3 domain containing 1 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17351624 1320081 Sorbs1 sorbin and SH3 domain containing 1 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17351624 1320081 Sorbs1 sorbin and SH3 domain containing 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17351624 1320081 Sorbs1 sorbin and SH3 domain containing 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:17351624 1320081 Sorbs1 sorbin and SH3 domain containing 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17351624 1320081 Sorbs1 sorbin and SH3 domain containing 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17351624 1320081 Sorbs1 sorbin and SH3 domain containing 1 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17351624 1320081 Sorbs1 sorbin and SH3 domain containing 1 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:17351624 1320081 Sorbs1 sorbin and SH3 domain containing 1 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:17351624 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9176491 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9259577 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:9259577 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:15803212 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9176491 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9259577 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:9259577 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:9176491 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:9259577 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9176491 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:15803212 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:9176491 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:9259577 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:9550720 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9176491 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15803212 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9176491 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9259577 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9550720 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9550720 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:9259577 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:9550720 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:15803212 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:9176491 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:9259577 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:16329126 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:16329126 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:9550720 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0006002 abnormal small intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:16329126 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:9259577 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0009480 distended cecum IAGP N RGD:5509061 20141003 MGI PMID:15803212 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0009480 distended cecum IAGP N RGD:5509061 20141003 MGI PMID:9176491 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0009485 distended ileum IAGP N RGD:5509061 20141003 MGI PMID:9176491 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9550720 1320083 Tlx2 T cell leukemia, homeobox 2 gene MP:0011881 distended duodenum IAGP N RGD:5509061 20150702 MGI PMID:16329126 1320085 Guk1 guanylate kinase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1320087 Gys1 glycogen synthase 1, muscle gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:15282316 1320087 Gys1 glycogen synthase 1, muscle gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15282316 1320087 Gys1 glycogen synthase 1, muscle gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:15282316 1320087 Gys1 glycogen synthase 1, muscle gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15282316 1320087 Gys1 glycogen synthase 1, muscle gene MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20151217 MGI PMID:24452334 1320087 Gys1 glycogen synthase 1, muscle gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20220331 MGI PMID:33219378 1320087 Gys1 glycogen synthase 1, muscle gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1320087 Gys1 glycogen synthase 1, muscle gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20160602 MGI PMID:23281428 1320087 Gys1 glycogen synthase 1, muscle gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20151217 MGI PMID:24452334 1320087 Gys1 glycogen synthase 1, muscle gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1320087 Gys1 glycogen synthase 1, muscle gene MP:0001785 edema IEA N RGD:5509061 20221215 MGI 1320087 Gys1 glycogen synthase 1, muscle gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20160602 MGI PMID:23281428 1320087 Gys1 glycogen synthase 1, muscle gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:15282316 1320087 Gys1 glycogen synthase 1, muscle gene MP:0002714 increased glycogen catabolism rate IAGP N RGD:5509061 20141003 MGI PMID:21035757 1320087 Gys1 glycogen synthase 1, muscle gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20160602 MGI PMID:23281428 1320087 Gys1 glycogen synthase 1, muscle gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:15282316 1320087 Gys1 glycogen synthase 1, muscle gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20160602 MGI PMID:23281428 1320087 Gys1 glycogen synthase 1, muscle gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:15282316 1320087 Gys1 glycogen synthase 1, muscle gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15282316 1320087 Gys1 glycogen synthase 1, muscle gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20151217 MGI PMID:24452334 1320087 Gys1 glycogen synthase 1, muscle gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15282316 1320087 Gys1 glycogen synthase 1, muscle gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15282316 1320087 Gys1 glycogen synthase 1, muscle gene MP:0004130 abnormal muscle cell glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:21035757 1320087 Gys1 glycogen synthase 1, muscle gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15282316 1320087 Gys1 glycogen synthase 1, muscle gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21035757 1320087 Gys1 glycogen synthase 1, muscle gene MP:0005439 decreased glycogen level IAGP N RGD:5509061 20141003 MGI PMID:15282316 1320087 Gys1 glycogen synthase 1, muscle gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20151217 MGI PMID:24452334 1320087 Gys1 glycogen synthase 1, muscle gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15282316 1320087 Gys1 glycogen synthase 1, muscle gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:21035757 1320087 Gys1 glycogen synthase 1, muscle gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15282316 1320087 Gys1 glycogen synthase 1, muscle gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20151126 MGI PMID:25059425 1320087 Gys1 glycogen synthase 1, muscle gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1320087 Gys1 glycogen synthase 1, muscle gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1320087 Gys1 glycogen synthase 1, muscle gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20221215 MGI 1320087 Gys1 glycogen synthase 1, muscle gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:15282316 1320087 Gys1 glycogen synthase 1, muscle gene MP:0014075 decreased brain glycogen level IAGP N RGD:5509061 20160602 MGI PMID:23281428 1320087 Gys1 glycogen synthase 1, muscle gene MP:0031007 decreased lung glycogen level IAGP N RGD:5509061 20220331 MGI PMID:33219378 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:1283314 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10415348 1320089 Smarcad1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1320092 Adat2 adenosine deaminase, tRNA-specific 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1320093 Ap5z1 adaptor-related protein complex 5, zeta 1 subunit gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20201231 MGI 1320093 Ap5z1 adaptor-related protein complex 5, zeta 1 subunit gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20201015 MGI PMID:30930081 1320093 Ap5z1 adaptor-related protein complex 5, zeta 1 subunit gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20201015 MGI PMID:30930081 1320093 Ap5z1 adaptor-related protein complex 5, zeta 1 subunit gene MP:0001406 abnormal gait IAGP N RGD:5509061 20201015 MGI PMID:30930081 1320093 Ap5z1 adaptor-related protein complex 5, zeta 1 subunit gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20201015 MGI PMID:30930081 1320093 Ap5z1 adaptor-related protein complex 5, zeta 1 subunit gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20201015 MGI PMID:30930081 1320093 Ap5z1 adaptor-related protein complex 5, zeta 1 subunit gene MP:0003354 astrocytosis IAGP N RGD:5509061 20201015 MGI PMID:30930081 1320093 Ap5z1 adaptor-related protein complex 5, zeta 1 subunit gene MP:0005405 axon degeneration IAGP N RGD:5509061 20201015 MGI PMID:30930081 1320093 Ap5z1 adaptor-related protein complex 5, zeta 1 subunit gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20201015 MGI PMID:30930081 1320093 Ap5z1 adaptor-related protein complex 5, zeta 1 subunit gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20201015 MGI PMID:30930081 1320093 Ap5z1 adaptor-related protein complex 5, zeta 1 subunit gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20201015 MGI PMID:30930081 1320093 Ap5z1 adaptor-related protein complex 5, zeta 1 subunit gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:30930081 1320093 Ap5z1 adaptor-related protein complex 5, zeta 1 subunit gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20201015 MGI PMID:30930081 1320093 Ap5z1 adaptor-related protein complex 5, zeta 1 subunit gene MP:0030949 abnormal Golgi vesicle transport IAGP N RGD:5509061 20201015 MGI PMID:30930081 1320093 Ap5z1 adaptor-related protein complex 5, zeta 1 subunit gene MP:0030952 abnormal Golgi stack morphology IAGP N RGD:5509061 20201015 MGI PMID:30930081 1320097 Aga aspartylglucosaminidase gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:8946839 1320097 Aga aspartylglucosaminidase gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9425233 1320097 Aga aspartylglucosaminidase gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:9425233 1320097 Aga aspartylglucosaminidase gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:8946839 1320097 Aga aspartylglucosaminidase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:9425233 1320097 Aga aspartylglucosaminidase gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0001655 multifocal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0003624 anuria IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0004195 abnormal kidney calyx morphology IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:8946839 1320097 Aga aspartylglucosaminidase gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:9425233 1320097 Aga aspartylglucosaminidase gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:9686358 1320097 Aga aspartylglucosaminidase gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0005302 neurogenic bladder IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:8946839 1320097 Aga aspartylglucosaminidase gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:9425233 1320097 Aga aspartylglucosaminidase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10657992 1320097 Aga aspartylglucosaminidase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8946839 1320097 Aga aspartylglucosaminidase gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:9425233 1320097 Aga aspartylglucosaminidase gene MP:0011413 colorless urine IAGP N RGD:5509061 20141003 MGI PMID:9777961 1320097 Aga aspartylglucosaminidase gene MP:0011516 aspartylglucosaminuria IAGP N RGD:5509061 20141003 MGI PMID:8946839 1320097 Aga aspartylglucosaminidase gene MP:0011516 aspartylglucosaminuria IAGP N RGD:5509061 20141003 MGI PMID:9425233 1320099 Magel2 MAGE family member L2 gene MP:0000161 scoliosis IAGP N RGD:5509061 20160804 MGI PMID:27436578 1320099 Magel2 MAGE family member L2 gene MP:0001261 obese IAGP N RGD:5509061 20160804 MGI PMID:27436578 1320099 Magel2 MAGE family member L2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20876615 1320099 Magel2 MAGE family member L2 gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:19172181 1320099 Magel2 MAGE family member L2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20230119 MGI 1320099 Magel2 MAGE family member L2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17893678 1320099 Magel2 MAGE family member L2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160804 MGI PMID:27436578 1320099 Magel2 MAGE family member L2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:20876615 1320099 Magel2 MAGE family member L2 gene MP:0001752 abnormal hypothalamus secretion IAGP N RGD:5509061 20141003 MGI PMID:20876615 1320099 Magel2 MAGE family member L2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17893678 1320099 Magel2 MAGE family member L2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19172181 1320099 Magel2 MAGE family member L2 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:19172181 1320099 Magel2 MAGE family member L2 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:19172181 1320099 Magel2 MAGE family member L2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20160804 MGI PMID:27436578 1320099 Magel2 MAGE family member L2 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:19172181 1320099 Magel2 MAGE family member L2 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:17893678 1320099 Magel2 MAGE family member L2 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:19172181 1320099 Magel2 MAGE family member L2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20160804 MGI PMID:27436578 1320099 Magel2 MAGE family member L2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230119 MGI 1320099 Magel2 MAGE family member L2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20876615 1320099 Magel2 MAGE family member L2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20230119 MGI 1320099 Magel2 MAGE family member L2 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20160804 MGI PMID:27436578 1320099 Magel2 MAGE family member L2 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:19172181 1320099 Magel2 MAGE family member L2 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:19172181 1320099 Magel2 MAGE family member L2 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:19172181 1320099 Magel2 MAGE family member L2 gene MP:0009008 delayed estrous cycle IAGP N RGD:5509061 20220630 MGI PMID:19172181 1320099 Magel2 MAGE family member L2 gene MP:0009013 abnormal proestrus IAGP N RGD:5509061 20141003 MGI PMID:19172181 1320099 Magel2 MAGE family member L2 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20160804 MGI PMID:27436578 1320099 Magel2 MAGE family member L2 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20160804 MGI PMID:27436578 1320099 Magel2 MAGE family member L2 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20160804 MGI PMID:27436578 1320099 Magel2 MAGE family member L2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:20876615 1320099 Magel2 MAGE family member L2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160804 MGI PMID:27436578 1320099 Magel2 MAGE family member L2 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20160804 MGI PMID:27436578 1320099 Magel2 MAGE family member L2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17893678 1320099 Magel2 MAGE family member L2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19172181 1320099 Magel2 MAGE family member L2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20876615 1320099 Magel2 MAGE family member L2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20160804 MGI PMID:27436578 1320099 Magel2 MAGE family member L2 gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:17893678 1320099 Magel2 MAGE family member L2 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20160804 MGI PMID:27436578 1320099 Magel2 MAGE family member L2 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:17893678 1320099 Magel2 MAGE family member L2 gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20171012 MGI PMID:17893678 1320102 Rlbp1 retinaldehyde binding protein 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:11301032 1320102 Rlbp1 retinaldehyde binding protein 1 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:11301032 1320102 Rlbp1 retinaldehyde binding protein 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11301032 1320102 Rlbp1 retinaldehyde binding protein 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20201231 MGI 1320102 Rlbp1 retinaldehyde binding protein 1 gene MP:0003011 delayed dark adaptation IAGP N RGD:5509061 20141003 MGI PMID:11301032 1320102 Rlbp1 retinaldehyde binding protein 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1320102 Rlbp1 retinaldehyde binding protein 1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:11301032 1320103 Efcab5 EF-hand calcium binding domain 5 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20220811 MGI 1320103 Efcab5 EF-hand calcium binding domain 5 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210520 MGI 1320103 Efcab5 EF-hand calcium binding domain 5 gene MP:0001148 enlarged testis IEA N RGD:5509061 20210520 MGI 1320103 Efcab5 EF-hand calcium binding domain 5 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20220811 MGI 1320108 Ptprt protein tyrosine phosphatase receptor type T gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20133777 1320108 Ptprt protein tyrosine phosphatase receptor type T gene MP:0002573 behavioral despair IAGP N RGD:5509061 20210429 MGI PMID:32938684 1320108 Ptprt protein tyrosine phosphatase receptor type T gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20210429 MGI PMID:32938684 1320108 Ptprt protein tyrosine phosphatase receptor type T gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:20133777 1320108 Ptprt protein tyrosine phosphatase receptor type T gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20210429 MGI PMID:32938684 1320108 Ptprt protein tyrosine phosphatase receptor type T gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20210429 MGI PMID:32938684 1320108 Ptprt protein tyrosine phosphatase receptor type T gene MP:0012207 decreased neuronal stem cell self-renewal IAGP N RGD:5509061 20210429 MGI PMID:32938684 1320108 Ptprt protein tyrosine phosphatase receptor type T gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:32938684 1320108 Ptprt protein tyrosine phosphatase receptor type T gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20210429 MGI PMID:32938684 1320108 Ptprt protein tyrosine phosphatase receptor type T gene MP:0020358 abnormal inhibitory synapse morphology IAGP N RGD:5509061 20210429 MGI PMID:32938684 1320108 Ptprt protein tyrosine phosphatase receptor type T gene MP:0030707 decreased glutamine level IAGP N RGD:5509061 20210429 MGI PMID:32938684 1320108 Ptprt protein tyrosine phosphatase receptor type T gene MP:0030733 decreased gamma-aminobutyric acid level IAGP N RGD:5509061 20210429 MGI PMID:32938684 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0000274 enlarged heart IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20221215 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0001262 decreased body weight IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0001297 microphthalmia IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210826 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0001406 abnormal gait IEA N RGD:5509061 20210826 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0001512 trunk curl IEA N RGD:5509061 20210826 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0001513 limb grasping IEA N RGD:5509061 20210826 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20210826 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0002188 small heart IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0002989 small kidney IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210826 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210826 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0005655 increased aggression IEA N RGD:5509061 20210826 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210826 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20230601 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0010935 increased airway resistance IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0011047 increased lung tissue damping IEA N RGD:5509061 20220519 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1320110 Sox14 SRY (sex determining region Y)-box 14 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210826 MGI 1320111 Cep95 centrosomal protein 95 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201231 MGI 1320111 Cep95 centrosomal protein 95 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201022 MGI 1320111 Cep95 centrosomal protein 95 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1320112 Tapt1 transmembrane anterior posterior transformation 1 gene MP:0000111 cleft palate IEA N RGD:5509061 20111116 MGI 1320112 Tapt1 transmembrane anterior posterior transformation 1 gene MP:0001577 anemia IEA N RGD:5509061 20111116 MGI 1320112 Tapt1 transmembrane anterior posterior transformation 1 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17151244 1320112 Tapt1 transmembrane anterior posterior transformation 1 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17151244 1320112 Tapt1 transmembrane anterior posterior transformation 1 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:17151244 1320112 Tapt1 transmembrane anterior posterior transformation 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16024820 1320112 Tapt1 transmembrane anterior posterior transformation 1 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:16024820 1320112 Tapt1 transmembrane anterior posterior transformation 1 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17151244 1320112 Tapt1 transmembrane anterior posterior transformation 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16024820 1320116 Snai3 snail family zinc finger 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0000692 small spleen IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0000706 small thymus IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0002083 premature death IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23762348 1320116 Snai3 snail family zinc finger 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20150409 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0014129 thymus fibrosis IAGP N RGD:5509061 20160324 MGI PMID:23874916 1320116 Snai3 snail family zinc finger 3 gene MP:0014350 disorganized spleen B cell follicle IAGP N RGD:5509061 20240104 MGI PMID:23874916 1320118 Arrdc2 arrestin domain containing 2 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20211021 MGI 1320118 Arrdc2 arrestin domain containing 2 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1320118 Arrdc2 arrestin domain containing 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20221215 MGI 1320119 Tmem161b transmembrane protein 161B gene MP:0000433 microcephaly IAGP N RGD:5509061 20230907 MGI PMID:36669109 1320119 Tmem161b transmembrane protein 161B gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20230907 MGI PMID:36669109 1320119 Tmem161b transmembrane protein 161B gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20230907 MGI PMID:36669109 1320119 Tmem161b transmembrane protein 161B gene MP:0003104 acrania IAGP N RGD:5509061 20230907 MGI PMID:36669109 1320119 Tmem161b transmembrane protein 161B gene MP:0003631 nervous system phenotype IAGP N RGD:5509061 20230907 MGI PMID:36669109 1320119 Tmem161b transmembrane protein 161B gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20230907 MGI PMID:36669109 1320119 Tmem161b transmembrane protein 161B gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1320119 Tmem161b transmembrane protein 161B gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20230907 MGI PMID:36669109 1320119 Tmem161b transmembrane protein 161B gene MP:0005390 skeleton phenotype IAGP N RGD:5509061 20230907 MGI PMID:36669109 1320119 Tmem161b transmembrane protein 161B gene MP:0005391 vision/eye phenotype IAGP N RGD:5509061 20230907 MGI PMID:36669109 1320119 Tmem161b transmembrane protein 161B gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1320119 Tmem161b transmembrane protein 161B gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20230907 MGI PMID:36669109 1320119 Tmem161b transmembrane protein 161B gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 1320119 Tmem161b transmembrane protein 161B gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20230907 MGI PMID:36669109 1320119 Tmem161b transmembrane protein 161B gene MP:0009268 absent cerebellum fissure IAGP N RGD:5509061 20230907 MGI PMID:36669109 1320119 Tmem161b transmembrane protein 161B gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1320119 Tmem161b transmembrane protein 161B gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230601 MGI 1320119 Tmem161b transmembrane protein 161B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 1320119 Tmem161b transmembrane protein 161B gene MP:0030192 downturned snout IAGP N RGD:5509061 20230907 MGI PMID:36669109 1320121 Klhl5 kelch-like 5 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20200514 MGI 1320121 Klhl5 kelch-like 5 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20210128 MGI 1320121 Klhl5 kelch-like 5 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20200514 MGI 1320121 Klhl5 kelch-like 5 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210128 MGI 1320121 Klhl5 kelch-like 5 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200514 MGI 1320121 Klhl5 kelch-like 5 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1320123 E2f3 E2F transcription factor 3 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:18663357 1320123 E2f3 E2F transcription factor 3 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18663357 1320123 E2f3 E2F transcription factor 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10733529 1320123 E2f3 E2F transcription factor 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18663357 1320123 E2f3 E2F transcription factor 3 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:11909960 1320123 E2f3 E2F transcription factor 3 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201231 MGI 1320123 E2f3 E2F transcription factor 3 gene MP:0000771 abnormal brain size IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18663357 1320123 E2f3 E2F transcription factor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:17608565 1320123 E2f3 E2F transcription factor 3 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1320123 E2f3 E2F transcription factor 3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210826 MGI 1320123 E2f3 E2F transcription factor 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200402 MGI 1320123 E2f3 E2F transcription factor 3 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:11909960 1320123 E2f3 E2F transcription factor 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:11909960 1320123 E2f3 E2F transcription factor 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11909960 1320123 E2f3 E2F transcription factor 3 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11909960 1320123 E2f3 E2F transcription factor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18663357 1320123 E2f3 E2F transcription factor 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:18663357 1320123 E2f3 E2F transcription factor 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:10733529 1320123 E2f3 E2F transcription factor 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18663357 1320123 E2f3 E2F transcription factor 3 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:11909960 1320123 E2f3 E2F transcription factor 3 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:11909960 1320123 E2f3 E2F transcription factor 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20230601 MGI 1320123 E2f3 E2F transcription factor 3 gene MP:0004002 abnormal jejunum morphology IEA N RGD:5509061 20210826 MGI 1320123 E2f3 E2F transcription factor 3 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0005158 ovary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17608565 1320123 E2f3 E2F transcription factor 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10733529 1320123 E2f3 E2F transcription factor 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11511364 1320123 E2f3 E2F transcription factor 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18663357 1320123 E2f3 E2F transcription factor 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17608565 1320123 E2f3 E2F transcription factor 3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:11909960 1320123 E2f3 E2F transcription factor 3 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:17608565 1320123 E2f3 E2F transcription factor 3 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20141003 MGI PMID:17608565 1320123 E2f3 E2F transcription factor 3 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11909960 1320123 E2f3 E2F transcription factor 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:11909960 1320123 E2f3 E2F transcription factor 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220519 MGI 1320123 E2f3 E2F transcription factor 3 gene MP:0010334 pleural effusion IAGP N RGD:5509061 20141003 MGI PMID:11909960 1320123 E2f3 E2F transcription factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10733529 1320123 E2f3 E2F transcription factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11909960 1320123 E2f3 E2F transcription factor 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18663357 1320123 E2f3 E2F transcription factor 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18594513 1320123 E2f3 E2F transcription factor 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11909960 1320123 E2f3 E2F transcription factor 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11909960 1320123 E2f3 E2F transcription factor 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320123 E2f3 E2F transcription factor 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11511364 1320123 E2f3 E2F transcription factor 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11909960 1320123 E2f3 E2F transcription factor 3 gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20161124 MGI PMID:11909960 1320132 Sf3b4 splicing factor 3b, subunit 4 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20200402 MGI PMID:31900962 1320132 Sf3b4 splicing factor 3b, subunit 4 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20200402 MGI PMID:31900962 1320132 Sf3b4 splicing factor 3b, subunit 4 gene MP:0000480 increased rib number IAGP N RGD:5509061 20200402 MGI PMID:31900962 1320132 Sf3b4 splicing factor 3b, subunit 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200402 MGI PMID:31900962 1320132 Sf3b4 splicing factor 3b, subunit 4 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20200402 MGI PMID:31900962 1320132 Sf3b4 splicing factor 3b, subunit 4 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20200402 MGI PMID:31900962 1320132 Sf3b4 splicing factor 3b, subunit 4 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20200402 MGI PMID:31900962 1320132 Sf3b4 splicing factor 3b, subunit 4 gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20200402 MGI PMID:31900962 1320132 Sf3b4 splicing factor 3b, subunit 4 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200402 MGI PMID:31900962 1320132 Sf3b4 splicing factor 3b, subunit 4 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20200402 MGI PMID:31900962 1320132 Sf3b4 splicing factor 3b, subunit 4 gene MP:0012174 flat head IAGP N RGD:5509061 20200402 MGI PMID:31900962 1320132 Sf3b4 splicing factor 3b, subunit 4 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20200402 MGI PMID:31900962 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20180920 MGI PMID:21247897 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20190221 MGI PMID:30653527 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20190221 MGI PMID:30653527 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180920 MGI PMID:21247897 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190221 MGI PMID:30653527 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20190221 MGI PMID:30653527 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20190221 MGI PMID:30653527 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0002223 lymphoid hypoplasia IAGP N RGD:5509061 20180920 MGI PMID:21247897 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20190221 MGI PMID:30653527 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20190221 MGI PMID:30653527 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20190221 MGI PMID:30653527 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20190221 MGI PMID:30653527 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20190221 MGI PMID:30653527 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20190221 MGI PMID:30653527 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20190221 MGI PMID:30653527 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20190221 MGI PMID:30653527 1320133 Dcun1d1 defective in cullin neddylation 1 domain containing 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20180920 MGI PMID:21247897 1320135 Dnal1 dynein, axonemal, light chain 1 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20170504 MGI 1320135 Dnal1 dynein, axonemal, light chain 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1320135 Dnal1 dynein, axonemal, light chain 1 gene MP:0002581 abnormal ileum morphology IEA N RGD:5509061 20170504 MGI 1320135 Dnal1 dynein, axonemal, light chain 1 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20210520 MGI 1320135 Dnal1 dynein, axonemal, light chain 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20170504 MGI 1320135 Dnal1 dynein, axonemal, light chain 1 gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20210128 MGI 1320135 Dnal1 dynein, axonemal, light chain 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170504 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0000277 abnormal heart shape IEA N RGD:5509061 20210520 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210826 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20201022 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0000601 small liver IEA N RGD:5509061 20201022 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0009084 blind uterus IEA N RGD:5509061 20210826 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210826 MGI 1320137 Zfp236 zinc finger protein 236 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1320145 Sox13 SRY (sex determining region Y)-box 13 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17218525 1320145 Sox13 SRY (sex determining region Y)-box 13 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:17218525 1320145 Sox13 SRY (sex determining region Y)-box 13 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1320145 Sox13 SRY (sex determining region Y)-box 13 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17218525 1320145 Sox13 SRY (sex determining region Y)-box 13 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 1320145 Sox13 SRY (sex determining region Y)-box 13 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17218525 1320149 Prxl2a peroxiredoxin like 2A gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20161027 MGI PMID:26629401 1320149 Prxl2a peroxiredoxin like 2A gene MP:0004892 increased adiponectin level IAGP N RGD:5509061 20161027 MGI PMID:26629401 1320149 Prxl2a peroxiredoxin like 2A gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20161027 MGI PMID:26629401 1320149 Prxl2a peroxiredoxin like 2A gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20161027 MGI PMID:26629401 1320149 Prxl2a peroxiredoxin like 2A gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20161027 MGI PMID:26629401 1320149 Prxl2a peroxiredoxin like 2A gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:26629401 1320149 Prxl2a peroxiredoxin like 2A gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240321 MGI PMID:26629401 1320151 Cd83 CD83 antigen gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1320151 Cd83 CD83 antigen gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1320151 Cd83 CD83 antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:11955430 1320151 Cd83 CD83 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11955430 1320151 Cd83 CD83 antigen gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11955430 1320151 Cd83 CD83 antigen gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11955430 1320151 Cd83 CD83 antigen gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18701714 1320151 Cd83 CD83 antigen gene MP:0004939 abnormal B cell morphology IEA N RGD:5509061 20111116 MGI 1320151 Cd83 CD83 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15322158 1320151 Cd83 CD83 antigen gene MP:0005461 abnormal dendritic cell morphology IEA N RGD:5509061 20111116 MGI 1320151 Cd83 CD83 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15322158 1320151 Cd83 CD83 antigen gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11955430 1320151 Cd83 CD83 antigen gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:15322158 1320151 Cd83 CD83 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11955430 1320151 Cd83 CD83 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20170706 MGI PMID:27503071 1320151 Cd83 CD83 antigen gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11955430 1320151 Cd83 CD83 antigen gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15322158 1320151 Cd83 CD83 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11955430 1320151 Cd83 CD83 antigen gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:11955430 1320151 Cd83 CD83 antigen gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:11955430 1320151 Cd83 CD83 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11955430 1320153 Colec11 collectin sub-family member 11 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20170706 MGI PMID:27088797 1320153 Colec11 collectin sub-family member 11 gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20170706 MGI PMID:27088797 1320153 Colec11 collectin sub-family member 11 gene MP:0005265 abnormal blood urea nitrogen level IAGP N RGD:5509061 20170706 MGI PMID:27088797 1320153 Colec11 collectin sub-family member 11 gene MP:0011566 abnormal complement protein level IAGP N RGD:5509061 20170706 MGI PMID:27088797 1320155 Thap12 THAP domain containing 12 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1320155 Thap12 THAP domain containing 12 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1320155 Thap12 THAP domain containing 12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:18413500 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0001333 absent optic nerve IEA N RGD:5509061 20210520 MGI 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:10864874 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:10864874 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:16636276 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:17360665 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:10864874 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0002188 small heart IEA N RGD:5509061 20201022 MGI 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0003194 abnormal frequency of paradoxical sleep IAGP N RGD:5509061 20141003 MGI PMID:16636276 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17360665 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:16636276 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:18413500 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17360665 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:18413500 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0005661 decreased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:17360665 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0005664 decreased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:17360665 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1320158 Npas2 neuronal PAS domain protein 2 gene MP:0021198 abnormal sleep duration IAGP N RGD:5509061 20220922 MGI PMID:16636276 1320159 Tmem209 transmembrane protein 209 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20181227 MGI 1320159 Tmem209 transmembrane protein 209 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20181227 MGI 1320159 Tmem209 transmembrane protein 209 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1320159 Tmem209 transmembrane protein 209 gene MP:0000914 exencephaly IEA N RGD:5509061 20210520 MGI 1320159 Tmem209 transmembrane protein 209 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1320159 Tmem209 transmembrane protein 209 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1320159 Tmem209 transmembrane protein 209 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1320159 Tmem209 transmembrane protein 209 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230601 MGI 1320159 Tmem209 transmembrane protein 209 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1320159 Tmem209 transmembrane protein 209 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 1320159 Tmem209 transmembrane protein 209 gene MP:0003717 pallor IEA N RGD:5509061 20230601 MGI 1320159 Tmem209 transmembrane protein 209 gene MP:0009263 abnormal eyelid fusion IEA N RGD:5509061 20221215 MGI 1320159 Tmem209 transmembrane protein 209 gene MP:0009908 protruding tongue IEA N RGD:5509061 20221215 MGI 1320159 Tmem209 transmembrane protein 209 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 1320159 Tmem209 transmembrane protein 209 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20221215 MGI 1320159 Tmem209 transmembrane protein 209 gene MP:0011496 abnormal head size IEA N RGD:5509061 20221215 MGI 1320160 Ppme1 protein phosphatase methylesterase 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1320160 Ppme1 protein phosphatase methylesterase 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:18596935 1320160 Ppme1 protein phosphatase methylesterase 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1320160 Ppme1 protein phosphatase methylesterase 1 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:18596935 1320160 Ppme1 protein phosphatase methylesterase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:18596935 1320160 Ppme1 protein phosphatase methylesterase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18596935 1320160 Ppme1 protein phosphatase methylesterase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:23791522 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:20622869 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0001192 scaly skin IEA N RGD:5509061 20210520 MGI 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20622869 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:23791522 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23791522 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23791522 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23791522 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23791522 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23791522 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:23791522 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23791522 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:20622870 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23791522 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20622870 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0010095 increased chromosomal stability IAGP N RGD:5509061 20141003 MGI PMID:20622869 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20141003 MGI PMID:20622869 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23791522 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20622870 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0011117 abnormal susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:23791522 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20170202 MGI PMID:23791522 1320162 Terf2ip telomeric repeat binding factor 2, interacting protein gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:20622869 1320163 Mif4gd MIF4G domain containing gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210520 MGI 1320169 Pprc1 peroxisome proliferative activated receptor, gamma, coactivator-related 1 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:22411706 1320169 Pprc1 peroxisome proliferative activated receptor, gamma, coactivator-related 1 gene MP:0003695 delayed blastocyst hatching from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:22411706 1320169 Pprc1 peroxisome proliferative activated receptor, gamma, coactivator-related 1 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:22411706 1320169 Pprc1 peroxisome proliferative activated receptor, gamma, coactivator-related 1 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:22411706 1320169 Pprc1 peroxisome proliferative activated receptor, gamma, coactivator-related 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22411706 1320171 Polr1c polymerase (RNA) I polypeptide C gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 1320171 Polr1c polymerase (RNA) I polypeptide C gene MP:0001513 limb grasping IEA N RGD:5509061 20210128 MGI 1320171 Polr1c polymerase (RNA) I polypeptide C gene MP:0001523 impaired righting response IEA N RGD:5509061 20210128 MGI 1320171 Polr1c polymerase (RNA) I polypeptide C gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 1320171 Polr1c polymerase (RNA) I polypeptide C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320171 Polr1c polymerase (RNA) I polypeptide C gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1320174 Jazf1 JAZF zinc finger 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1320174 Jazf1 JAZF zinc finger 1 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1320174 Jazf1 JAZF zinc finger 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20210422 MGI PMID:32640216 1320174 Jazf1 JAZF zinc finger 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20210422 MGI PMID:32640216 1320174 Jazf1 JAZF zinc finger 1 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20210422 MGI PMID:32640216 1320174 Jazf1 JAZF zinc finger 1 gene MP:0010147 abnormal endocrine pancreas physiology IAGP N RGD:5509061 20210422 MGI PMID:32640216 1320174 Jazf1 JAZF zinc finger 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1320174 Jazf1 JAZF zinc finger 1 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20210422 MGI PMID:32640216 1320174 Jazf1 JAZF zinc finger 1 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20210422 MGI PMID:32640216 1320174 Jazf1 JAZF zinc finger 1 gene MP:0014117 increased pancreatic beta cell apoptosis IAGP N RGD:5509061 20210422 MGI PMID:32640216 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20181206 MGI PMID:28655741 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20181206 MGI PMID:29116018 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0000410 waved hair IAGP N RGD:5509061 20150528 MGI PMID:12573256 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0000410 waved hair IAGP N RGD:5509061 20200827 MGI PMID:32646486 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20150528 MGI PMID:12573256 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20181206 MGI PMID:28655741 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20181206 MGI PMID:29116018 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0000416 sparse hair IAGP N RGD:5509061 20220602 MGI PMID:10425919 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20220519 MGI PMID:28128203 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:22246778 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20150528 MGI PMID:12573256 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20181206 MGI PMID:28655741 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20181206 MGI PMID:29116018 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20220602 MGI PMID:10425919 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0001214 skin hyperplasia IAGP N RGD:5509061 20181206 MGI PMID:28655741 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0001214 skin hyperplasia IAGP N RGD:5509061 20181206 MGI PMID:29116018 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20220519 MGI PMID:28128203 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20150528 MGI PMID:12573256 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20181206 MGI PMID:28655741 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20181206 MGI PMID:29116018 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20150528 MGI PMID:12573256 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20150528 MGI PMID:12573256 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20161103 MGI PMID:25918388 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20200827 MGI PMID:32646486 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20210128 MGI 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0001790 abnormal immune system physiology IEA N RGD:5509061 20141003 MGI 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220602 MGI PMID:10425919 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20181206 MGI PMID:28655741 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20161103 MGI PMID:25918388 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20210128 MGI 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:22246778 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20161103 MGI PMID:25918388 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22246778 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:22246778 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20181206 MGI PMID:28655741 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20181206 MGI PMID:29116018 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20161103 MGI PMID:25918388 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20181206 MGI PMID:28655741 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20181206 MGI PMID:29116018 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20161103 MGI PMID:25918388 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20150528 MGI PMID:12573256 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0003815 hairless IAGP N RGD:5509061 20220602 MGI PMID:10425919 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220602 MGI PMID:10425919 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20220602 MGI PMID:10425919 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22246777 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22246778 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22246777 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22246778 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22550345 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20161103 MGI PMID:25918388 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20161103 MGI PMID:25918388 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0009273 abnormal hair shaft melanin granule shape IAGP N RGD:5509061 20150528 MGI PMID:12573256 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0009786 decreased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22246778 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22246778 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20211021 MGI 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0010591 enlarged aortic valve IAGP N RGD:5509061 20161103 MGI PMID:25918388 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20161103 MGI PMID:25918388 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0010600 enlarged pulmonary valve IAGP N RGD:5509061 20161103 MGI PMID:25918388 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0010605 thick pulmonary valve cusps IAGP N RGD:5509061 20161103 MGI PMID:25918388 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0010626 thick tricuspid valve cusps IAGP N RGD:5509061 20161103 MGI PMID:25918388 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0010627 enlarged tricuspid valve IAGP N RGD:5509061 20161103 MGI PMID:25918388 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20150528 MGI PMID:12573256 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23969955 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20181206 MGI PMID:29116018 1320183 Rhbdf2 rhomboid 5 homolog 2 gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240418 MGI PMID:12573256 1320184 Smg5 SMG5 nonsense mediated mRNA decay factor gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1320184 Smg5 SMG5 nonsense mediated mRNA decay factor gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1320184 Smg5 SMG5 nonsense mediated mRNA decay factor gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1320184 Smg5 SMG5 nonsense mediated mRNA decay factor gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1320184 Smg5 SMG5 nonsense mediated mRNA decay factor gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1320184 Smg5 SMG5 nonsense mediated mRNA decay factor gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1320184 Smg5 SMG5 nonsense mediated mRNA decay factor gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1320184 Smg5 SMG5 nonsense mediated mRNA decay factor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20240926 MGI PMID:39199410 1320184 Smg5 SMG5 nonsense mediated mRNA decay factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320184 Smg5 SMG5 nonsense mediated mRNA decay factor gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1320184 Smg5 SMG5 nonsense mediated mRNA decay factor gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1320185 Fam114a1 family with sequence similarity 114, member A1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1320185 Fam114a1 family with sequence similarity 114, member A1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1320188 Adgrb3 adhesion G protein-coupled receptor B3 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20170518 MGI PMID:25611509 1320188 Adgrb3 adhesion G protein-coupled receptor B3 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20170518 MGI PMID:25611509 1320188 Adgrb3 adhesion G protein-coupled receptor B3 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20170518 MGI PMID:25611509 1320188 Adgrb3 adhesion G protein-coupled receptor B3 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20170518 MGI PMID:25611509 1320188 Adgrb3 adhesion G protein-coupled receptor B3 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20170518 MGI PMID:25611509 1320188 Adgrb3 adhesion G protein-coupled receptor B3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1320190 Bclaf1 BCL2-associated transcription factor 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19008920 1320190 Bclaf1 BCL2-associated transcription factor 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19008920 1320190 Bclaf1 BCL2-associated transcription factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19008920 1320190 Bclaf1 BCL2-associated transcription factor 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1320190 Bclaf1 BCL2-associated transcription factor 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1320190 Bclaf1 BCL2-associated transcription factor 1 gene MP:0001575 cyanosis IEA N RGD:5509061 20210520 MGI 1320190 Bclaf1 BCL2-associated transcription factor 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19008920 1320190 Bclaf1 BCL2-associated transcription factor 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19008920 1320190 Bclaf1 BCL2-associated transcription factor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19008920 1320190 Bclaf1 BCL2-associated transcription factor 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:19008920 1320190 Bclaf1 BCL2-associated transcription factor 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1320190 Bclaf1 BCL2-associated transcription factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19008920 1320190 Bclaf1 BCL2-associated transcription factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320190 Bclaf1 BCL2-associated transcription factor 1 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:19008920 1320190 Bclaf1 BCL2-associated transcription factor 1 gene MP:0011145 abnormal mesenchymal cell differentiation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:19008920 1320193 Vcf1 VCP nuclear cofactor family member 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1320193 Vcf1 VCP nuclear cofactor family member 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 1320195 Ccdc181 coiled-coil domain containing 181 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1320195 Ccdc181 coiled-coil domain containing 181 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1320202 Cln6 ceroid-lipofuscinosis, neuronal 6 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:9600738 1320202 Cln6 ceroid-lipofuscinosis, neuronal 6 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:9600738 1320202 Cln6 ceroid-lipofuscinosis, neuronal 6 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1320202 Cln6 ceroid-lipofuscinosis, neuronal 6 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:9600738 1320202 Cln6 ceroid-lipofuscinosis, neuronal 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9600738 1320202 Cln6 ceroid-lipofuscinosis, neuronal 6 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 1320202 Cln6 ceroid-lipofuscinosis, neuronal 6 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:9600738 1320202 Cln6 ceroid-lipofuscinosis, neuronal 6 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141127 MGI PMID:24423645 1320202 Cln6 ceroid-lipofuscinosis, neuronal 6 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:9600738 1320202 Cln6 ceroid-lipofuscinosis, neuronal 6 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20231207 MGI 1320202 Cln6 ceroid-lipofuscinosis, neuronal 6 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:9600738 1320202 Cln6 ceroid-lipofuscinosis, neuronal 6 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1320202 Cln6 ceroid-lipofuscinosis, neuronal 6 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 1320202 Cln6 ceroid-lipofuscinosis, neuronal 6 gene MP:0031204 hindlimb paresis IAGP N RGD:5509061 20210218 MGI PMID:9600738 1320202 Cln6 ceroid-lipofuscinosis, neuronal 6 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:9600738 1320206 Ndfip2 Nedd4 family interacting protein 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20160421 MGI 1320206 Ndfip2 Nedd4 family interacting protein 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1320206 Ndfip2 Nedd4 family interacting protein 2 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1320206 Ndfip2 Nedd4 family interacting protein 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1320206 Ndfip2 Nedd4 family interacting protein 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 1320206 Ndfip2 Nedd4 family interacting protein 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1320206 Ndfip2 Nedd4 family interacting protein 2 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1320206 Ndfip2 Nedd4 family interacting protein 2 gene MP:0004152 abnormal circulating iron level IAGP N RGD:5509061 20161117 MGI PMID:27048792 1320206 Ndfip2 Nedd4 family interacting protein 2 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1320206 Ndfip2 Nedd4 family interacting protein 2 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20161117 MGI PMID:27048792 1320206 Ndfip2 Nedd4 family interacting protein 2 gene MP:0008738 abnormal liver iron level IAGP N RGD:5509061 20161117 MGI PMID:27048792 1320206 Ndfip2 Nedd4 family interacting protein 2 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20161117 MGI PMID:27048792 1320206 Ndfip2 Nedd4 family interacting protein 2 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20161117 MGI PMID:27048792 1320206 Ndfip2 Nedd4 family interacting protein 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1320206 Ndfip2 Nedd4 family interacting protein 2 gene MP:0011895 abnormal circulating unsaturated transferrin level IAGP N RGD:5509061 20161117 MGI PMID:27048792 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320215 Afg3l1 AFG3-like AAA ATPase 1 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20170126 MGI PMID:27911893 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:16571627 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:16116426 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231207 MGI PMID:32511952 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20231207 MGI PMID:32511952 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231207 MGI PMID:32511952 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16571627 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:16571627 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16571627 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16571627 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0002632 vestigial tail IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:16571627 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20231207 MGI PMID:32511952 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16571627 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0004407 increased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16116426 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16116426 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16571627 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16116426 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:16571627 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20231207 MGI PMID:32511952 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16571627 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16571627 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12421720 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:19008950 1320220 Dvl2 dishevelled segment polarity protein 2 gene MP:0012675 enlarged floor plate IAGP N RGD:5509061 20141003 MGI PMID:16571627 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:19564410 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17875667 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17875667 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21048139 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:21048139 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19564410 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17875667 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19564410 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:21048139 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21048139 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17875667 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21048139 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:21048139 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19564410 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:21048139 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17875667 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17875667 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21048139 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0003234 enhanced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21048139 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0004495 decreased synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:21048139 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21048139 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19564410 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:21048139 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:21048139 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21048139 1320223 Mapk8ip2 mitogen-activated protein kinase 8 interacting protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19564410 1320225 Cbr3 carbonyl reductase 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1320225 Cbr3 carbonyl reductase 3 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1320225 Cbr3 carbonyl reductase 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1320225 Cbr3 carbonyl reductase 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1320225 Cbr3 carbonyl reductase 3 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20211021 MGI 1320225 Cbr3 carbonyl reductase 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1320225 Cbr3 carbonyl reductase 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1320227 Iftap intraflagellar transport associated protein gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20201224 MGI PMID:30521625 1320227 Iftap intraflagellar transport associated protein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20201224 MGI PMID:30521625 1320227 Iftap intraflagellar transport associated protein gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20201224 MGI PMID:30521625 1320227 Iftap intraflagellar transport associated protein gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20201224 MGI PMID:30521625 1320227 Iftap intraflagellar transport associated protein gene MP:0009697 abnormal copulation behavior IAGP N RGD:5509061 20201224 MGI PMID:30521625 1320228 Mtss2 MTSS I-BAR domain containing 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1320228 Mtss2 MTSS I-BAR domain containing 2 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20200402 MGI 1320230 Matn4 matrilin 4 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1320230 Matn4 matrilin 4 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1320230 Matn4 matrilin 4 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1320230 Matn4 matrilin 4 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1320230 Matn4 matrilin 4 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1320230 Matn4 matrilin 4 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20210812 MGI PMID:27573814 1320230 Matn4 matrilin 4 gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20210812 MGI PMID:27573814 1320232 Nlrp9a NLR family, pyrin domain containing 9A gene MP:0001935 decreased litter size IAGP N RGD:5509061 20210415 MGI PMID:32413845 1320232 Nlrp9a NLR family, pyrin domain containing 9A gene MP:0002293 long gestation period IAGP N RGD:5509061 20210415 MGI PMID:32413845 1320232 Nlrp9a NLR family, pyrin domain containing 9A gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20210415 MGI PMID:32413845 1320232 Nlrp9a NLR family, pyrin domain containing 9A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20210415 MGI PMID:32413845 1320232 Nlrp9a NLR family, pyrin domain containing 9A gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20210415 MGI PMID:32413845 1320232 Nlrp9a NLR family, pyrin domain containing 9A gene MP:0012128 abnormal blastocyst formation IAGP N RGD:5509061 20210415 MGI PMID:32413845 1320232 Nlrp9a NLR family, pyrin domain containing 9A gene MP:0012129 failure of blastocyst formation IAGP N RGD:5509061 20210415 MGI PMID:32413845 1320233 Lamtor4 late endosomal/lysosomal adaptor, MAPK and MTOR activator 4 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20201231 MGI 1320233 Lamtor4 late endosomal/lysosomal adaptor, MAPK and MTOR activator 4 gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20200514 MGI 1320233 Lamtor4 late endosomal/lysosomal adaptor, MAPK and MTOR activator 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1320233 Lamtor4 late endosomal/lysosomal adaptor, MAPK and MTOR activator 4 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1320233 Lamtor4 late endosomal/lysosomal adaptor, MAPK and MTOR activator 4 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1320233 Lamtor4 late endosomal/lysosomal adaptor, MAPK and MTOR activator 4 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210520 MGI 1320233 Lamtor4 late endosomal/lysosomal adaptor, MAPK and MTOR activator 4 gene MP:0005355 enlarged thyroid gland IEA N RGD:5509061 20200514 MGI 1320233 Lamtor4 late endosomal/lysosomal adaptor, MAPK and MTOR activator 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320233 Lamtor4 late endosomal/lysosomal adaptor, MAPK and MTOR activator 4 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1320233 Lamtor4 late endosomal/lysosomal adaptor, MAPK and MTOR activator 4 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210520 MGI 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:23077216 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:23077216 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:23077216 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:23077216 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23077216 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:23077216 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23077216 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23077216 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:23077216 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:12955145 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:23077216 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:23077216 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23077216 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0004081 abnormal globus pallidus morphology IAGP N RGD:5509061 20141003 MGI PMID:23077216 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23077216 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:20548961 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:23077216 1320235 Zdhhc13 zinc finger, DHHC domain containing 13 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:23077216 1320239 Caskin2 CASK-interacting protein 2 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20211021 MGI 1320239 Caskin2 CASK-interacting protein 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20210603 MGI PMID:31727973 1320239 Caskin2 CASK-interacting protein 2 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20210603 MGI PMID:31727973 1320239 Caskin2 CASK-interacting protein 2 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 1320239 Caskin2 CASK-interacting protein 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1320239 Caskin2 CASK-interacting protein 2 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20210603 MGI PMID:31727973 1320239 Caskin2 CASK-interacting protein 2 gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20210603 MGI PMID:31727973 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:15520367 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:23918385 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0000265 blood vessel atresia IAGP N RGD:5509061 20141003 MGI PMID:15466160 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20231116 MGI PMID:33899511 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231116 MGI PMID:33899511 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:15466160 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:15520367 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:21498671 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:18824585 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:18824583 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15520367 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:23918385 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:15520367 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:15520367 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18824583 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18824585 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21598246 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18824583 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0002748 abnormal pulmonary valve morphology IAGP N RGD:5509061 20231116 MGI PMID:33899511 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23918385 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0003228 abnormal sinus venosus morphology IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0003230 abnormal umbilical artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:15520367 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0003410 abnormal artery development IAGP N RGD:5509061 20141003 MGI PMID:15520367 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0003411 abnormal vein development IAGP N RGD:5509061 20141003 MGI PMID:15520367 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:15466160 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:18824583 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15466160 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15466160 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15520367 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15466160 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0004786 abnormal common cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15466160 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15466160 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15520367 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18824583 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18824585 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:15466160 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15520367 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20141003 MGI PMID:15466160 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231116 MGI PMID:33899511 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18824585 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18824585 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18824585 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18824585 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:21498671 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231116 MGI PMID:33899511 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0010463 aorta stenosis IAGP N RGD:5509061 20141003 MGI PMID:15520367 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15466160 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15520367 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:15466159 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0012730 abnormal internal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15520367 1320242 Dll4 delta like canonical Notch ligand 4 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:15520367 1320246 Crtap cartilage associated protein gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:17055431 1320246 Crtap cartilage associated protein gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:17055431 1320246 Crtap cartilage associated protein gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17055431 1320246 Crtap cartilage associated protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17055431 1320246 Crtap cartilage associated protein gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:17055431 1320246 Crtap cartilage associated protein gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:17055431 1320246 Crtap cartilage associated protein gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:17055431 1320246 Crtap cartilage associated protein gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17055431 1320246 Crtap cartilage associated protein gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:17055431 1320246 Crtap cartilage associated protein gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:17055431 1320246 Crtap cartilage associated protein gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:17055431 1320246 Crtap cartilage associated protein gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:17055431 1320250 Zfp638 zinc finger protein 638 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1320250 Zfp638 zinc finger protein 638 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1320250 Zfp638 zinc finger protein 638 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20230601 MGI 1320250 Zfp638 zinc finger protein 638 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1320250 Zfp638 zinc finger protein 638 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1320252 Hapstr1 HUWE1 associated protein modifying stress responses gene MP:0001263 weight loss IAGP N RGD:5509061 20240620 MGI PMID:38453366 1320252 Hapstr1 HUWE1 associated protein modifying stress responses gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20240620 MGI PMID:38453366 1320252 Hapstr1 HUWE1 associated protein modifying stress responses gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20240620 MGI PMID:38453366 1320252 Hapstr1 HUWE1 associated protein modifying stress responses gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20240620 MGI PMID:38453366 1320252 Hapstr1 HUWE1 associated protein modifying stress responses gene MP:0009480 distended cecum IAGP N RGD:5509061 20240620 MGI PMID:38453366 1320252 Hapstr1 HUWE1 associated protein modifying stress responses gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240620 MGI PMID:38453366 1320252 Hapstr1 HUWE1 associated protein modifying stress responses gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20240620 MGI PMID:38453366 1320252 Hapstr1 HUWE1 associated protein modifying stress responses gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20240620 MGI PMID:38453366 1320253 Trim16 tripartite motif-containing 16 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1320253 Trim16 tripartite motif-containing 16 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20201231 MGI PMID:31342168 1320253 Trim16 tripartite motif-containing 16 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1320253 Trim16 tripartite motif-containing 16 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1320253 Trim16 tripartite motif-containing 16 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20201231 MGI PMID:31342168 1320253 Trim16 tripartite motif-containing 16 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20201231 MGI PMID:31342168 1320253 Trim16 tripartite motif-containing 16 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 1320253 Trim16 tripartite motif-containing 16 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20201231 MGI PMID:31342168 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20240822 MGI PMID:36053215 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20240822 MGI PMID:36053215 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0004882 enlarged lung IEA N RGD:5509061 20230601 MGI 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20240822 MGI PMID:36053215 1320259 Vamp4 vesicle-associated membrane protein 4 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240822 MGI PMID:36053215 1320261 Slfn1 schlafen 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9846487 1320261 Slfn1 schlafen 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1320261 Slfn1 schlafen 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1320261 Slfn1 schlafen 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1320263 Rgl3 ral guanine nucleotide dissociation stimulator-like 3 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 1320263 Rgl3 ral guanine nucleotide dissociation stimulator-like 3 gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 1320263 Rgl3 ral guanine nucleotide dissociation stimulator-like 3 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1320265 Cd72 CD72 antigen gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0004795 decreased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0004798 decreased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0006315 abnormal urine protein level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:10549631 1320265 Cd72 CD72 antigen gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:23616572 1320265 Cd72 CD72 antigen gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:23616572 1320267 Exosc7 exosome component 7 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241010 MGI 1320267 Exosc7 exosome component 7 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1320267 Exosc7 exosome component 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1320269 Ginm1 glycoprotein integral membrane 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1320269 Ginm1 glycoprotein integral membrane 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1320269 Ginm1 glycoprotein integral membrane 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20240523 MGI 1320269 Ginm1 glycoprotein integral membrane 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1320269 Ginm1 glycoprotein integral membrane 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1320271 Traip TRAF-interacting protein gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17927961 1320271 Traip TRAF-interacting protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17927961 1320271 Traip TRAF-interacting protein gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17927961 1320271 Traip TRAF-interacting protein gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17927961 1320271 Traip TRAF-interacting protein gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17927961 1320271 Traip TRAF-interacting protein gene MP:0011198 absent proamniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:17927961 1320271 Traip TRAF-interacting protein gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17927961 1320276 Trappc11 trafficking protein particle complex 11 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1320276 Trappc11 trafficking protein particle complex 11 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230601 MGI 1320276 Trappc11 trafficking protein particle complex 11 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1320276 Trappc11 trafficking protein particle complex 11 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1320281 Ahcyl1 S-adenosylhomocysteine hydrolase-like 1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20150108 MGI 1320281 Ahcyl1 S-adenosylhomocysteine hydrolase-like 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1320281 Ahcyl1 S-adenosylhomocysteine hydrolase-like 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 1320281 Ahcyl1 S-adenosylhomocysteine hydrolase-like 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1320281 Ahcyl1 S-adenosylhomocysteine hydrolase-like 1 gene MP:0005477 increased circulating thyroxine level IEA N RGD:5509061 20210128 MGI 1320281 Ahcyl1 S-adenosylhomocysteine hydrolase-like 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1320281 Ahcyl1 S-adenosylhomocysteine hydrolase-like 1 gene MP:0010148 abnormal exocrine pancreas physiology IAGP N RGD:5509061 20151119 MGI PMID:23542070 1320283 Bbx bobby sox HMG box containing gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20160922 MGI PMID:24652767 1320283 Bbx bobby sox HMG box containing gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20160804 MGI 1320283 Bbx bobby sox HMG box containing gene MP:0001258 decreased body length IAGP N RGD:5509061 20160922 MGI PMID:24652767 1320283 Bbx bobby sox HMG box containing gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1320283 Bbx bobby sox HMG box containing gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1320283 Bbx bobby sox HMG box containing gene MP:0002495 increased IgA level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1320283 Bbx bobby sox HMG box containing gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20160922 MGI PMID:24652767 1320283 Bbx bobby sox HMG box containing gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20160922 MGI PMID:24652767 1320283 Bbx bobby sox HMG box containing gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20160922 MGI PMID:24652767 1320283 Bbx bobby sox HMG box containing gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20160922 MGI PMID:24652767 1320283 Bbx bobby sox HMG box containing gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20160922 MGI PMID:24652767 1320285 Adamts15 ADAM metallopeptidase with thrombospondin type 1 motif 15 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1320285 Adamts15 ADAM metallopeptidase with thrombospondin type 1 motif 15 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20231207 MGI 1320285 Adamts15 ADAM metallopeptidase with thrombospondin type 1 motif 15 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1320285 Adamts15 ADAM metallopeptidase with thrombospondin type 1 motif 15 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20181227 MGI 1320287 Rpl27a ribosomal protein L27A gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21674502 1320287 Rpl27a ribosomal protein L27A gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:21674502 1320289 Api5 apoptosis inhibitor 5 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20231221 MGI PMID:36198790 1320289 Api5 apoptosis inhibitor 5 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20231221 MGI PMID:36198790 1320289 Api5 apoptosis inhibitor 5 gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20231221 MGI PMID:36198790 1320292 Zcchc8 zinc finger, CCHC domain containing 8 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20210610 MGI PMID:31747613 1320292 Zcchc8 zinc finger, CCHC domain containing 8 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20210610 MGI PMID:31747613 1320292 Zcchc8 zinc finger, CCHC domain containing 8 gene MP:0001127 small ovary IAGP N RGD:5509061 20210610 MGI PMID:31747613 1320292 Zcchc8 zinc finger, CCHC domain containing 8 gene MP:0001147 small testis IAGP N RGD:5509061 20210610 MGI PMID:31747613 1320292 Zcchc8 zinc finger, CCHC domain containing 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210610 MGI PMID:31747613 1320292 Zcchc8 zinc finger, CCHC domain containing 8 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210610 MGI PMID:31747613 1320292 Zcchc8 zinc finger, CCHC domain containing 8 gene MP:0001924 infertility IAGP N RGD:5509061 20210610 MGI PMID:31747613 1320292 Zcchc8 zinc finger, CCHC domain containing 8 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20210610 MGI PMID:31747613 1320292 Zcchc8 zinc finger, CCHC domain containing 8 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210610 MGI PMID:31747613 1320292 Zcchc8 zinc finger, CCHC domain containing 8 gene MP:0003718 maternal effect IAGP N RGD:5509061 20210610 MGI PMID:31747613 1320292 Zcchc8 zinc finger, CCHC domain containing 8 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20210610 MGI PMID:31747613 1320292 Zcchc8 zinc finger, CCHC domain containing 8 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20210610 MGI PMID:31747613 1320292 Zcchc8 zinc finger, CCHC domain containing 8 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20210610 MGI PMID:31747613 1320292 Zcchc8 zinc finger, CCHC domain containing 8 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20210610 MGI PMID:31747613 1320292 Zcchc8 zinc finger, CCHC domain containing 8 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20210610 MGI PMID:31747613 1320296 Il7r interleukin 7 receptor gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7964471 1320296 Il7r interleukin 7 receptor gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23267098 1320296 Il7r interleukin 7 receptor gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11034372 1320296 Il7r interleukin 7 receptor gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11123301 1320296 Il7r interleukin 7 receptor gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17325202 1320296 Il7r interleukin 7 receptor gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7964471 1320296 Il7r interleukin 7 receptor gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7964471 1320296 Il7r interleukin 7 receptor gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7964471 1320296 Il7r interleukin 7 receptor gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20151224 MGI PMID:24509509 1320296 Il7r interleukin 7 receptor gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17325202 1320296 Il7r interleukin 7 receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20303297 1320296 Il7r interleukin 7 receptor gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:9488150 1320296 Il7r interleukin 7 receptor gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267098 1320296 Il7r interleukin 7 receptor gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17325202 1320296 Il7r interleukin 7 receptor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:7964471 1320296 Il7r interleukin 7 receptor gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:7964471 1320296 Il7r interleukin 7 receptor gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17325202 1320296 Il7r interleukin 7 receptor gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17325202 1320296 Il7r interleukin 7 receptor gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17325202 1320296 Il7r interleukin 7 receptor gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11123301 1320296 Il7r interleukin 7 receptor gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17325202 1320296 Il7r interleukin 7 receptor gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23267098 1320296 Il7r interleukin 7 receptor gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:23267098 1320296 Il7r interleukin 7 receptor gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:17325202 1320296 Il7r interleukin 7 receptor gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17325202 1320296 Il7r interleukin 7 receptor gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23267098 1320296 Il7r interleukin 7 receptor gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17325202 1320296 Il7r interleukin 7 receptor gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23109710 1320296 Il7r interleukin 7 receptor gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23267098 1320296 Il7r interleukin 7 receptor gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7964471 1320296 Il7r interleukin 7 receptor gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23267098 1320296 Il7r interleukin 7 receptor gene MP:0008355 absent mature gamma-delta T cells IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0008356 abnormal gamma-delta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8692964 1320296 Il7r interleukin 7 receptor gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11123301 1320298 Mrc2 mannose receptor, C type 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12668656 1320298 Mrc2 mannose receptor, C type 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17596337 1320298 Mrc2 mannose receptor, C type 2 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:12835757 1320300 Snx13 sorting nexin 13 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1320300 Snx13 sorting nexin 13 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17077144 1320300 Snx13 sorting nexin 13 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17077144 1320300 Snx13 sorting nexin 13 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17077144 1320300 Snx13 sorting nexin 13 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:17077144 1320300 Snx13 sorting nexin 13 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:17077144 1320300 Snx13 sorting nexin 13 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:17077144 1320300 Snx13 sorting nexin 13 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17077144 1320300 Snx13 sorting nexin 13 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 1320300 Snx13 sorting nexin 13 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:17077144 1320300 Snx13 sorting nexin 13 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:17077144 1320300 Snx13 sorting nexin 13 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17077144 1320300 Snx13 sorting nexin 13 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17077144 1320300 Snx13 sorting nexin 13 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17077144 1320300 Snx13 sorting nexin 13 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1320303 Car1 carbonic anhydrase 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20241003 MGI PMID:37013604 1320303 Car1 carbonic anhydrase 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20241003 MGI PMID:37013604 1320303 Car1 carbonic anhydrase 1 gene MP:0008269 abnormal hippocampus CA4 region morphology IAGP N RGD:5509061 20241003 MGI PMID:37013604 1320303 Car1 carbonic anhydrase 1 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20241003 MGI PMID:37013604 1320303 Car1 carbonic anhydrase 1 gene MP:0014414 increased depression-related behavior IAGP N RGD:5509061 20241003 MGI PMID:37013604 1320303 Car1 carbonic anhydrase 1 gene MP:0021009 abnormal synaptic physiology IAGP N RGD:5509061 20241003 MGI PMID:37013604 1320307 Eed embryonic ectoderm development gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:19941827 1320307 Eed embryonic ectoderm development gene MP:0000371 diluted coat color IEA N RGD:5509061 20111116 MGI 1320307 Eed embryonic ectoderm development gene MP:0002427 disproportionate dwarf IEA N RGD:5509061 20111116 MGI 1320312 Tprkb Tp53rk binding protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20221124 MGI PMID:34849815 1320312 Tprkb Tp53rk binding protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1320314 Stam signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:11340172 1320314 Stam signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11340172 1320314 Stam signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11340172 1320314 Stam signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11340172 1320314 Stam signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:11340172 1320314 Stam signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:11340172 1320314 Stam signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 gene MP:0003415 priapism IAGP N RGD:5509061 20141003 MGI PMID:11340172 1320314 Stam signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12446783 1320314 Stam signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12446783 1320314 Stam signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:11340172 1320314 Stam signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12446783 1320316 Tesmin testis expressed metallothionein like gene MP:0001147 small testis IAGP N RGD:5509061 20200716 MGI PMID:31916570 1320316 Tesmin testis expressed metallothionein like gene MP:0001147 small testis IAGP N RGD:5509061 20220811 MGI PMID:34388164 1320316 Tesmin testis expressed metallothionein like gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20200716 MGI PMID:31916570 1320316 Tesmin testis expressed metallothionein like gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220811 MGI PMID:34388164 1320316 Tesmin testis expressed metallothionein like gene MP:0001925 male infertility IAGP N RGD:5509061 20200716 MGI PMID:31916570 1320316 Tesmin testis expressed metallothionein like gene MP:0001925 male infertility IAGP N RGD:5509061 20220811 MGI PMID:34388164 1320316 Tesmin testis expressed metallothionein like gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200716 MGI PMID:31916570 1320316 Tesmin testis expressed metallothionein like gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220811 MGI PMID:34388164 1320316 Tesmin testis expressed metallothionein like gene MP:0005159 azoospermia IAGP N RGD:5509061 20220811 MGI PMID:34388164 1320316 Tesmin testis expressed metallothionein like gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220811 MGI PMID:34388164 1320316 Tesmin testis expressed metallothionein like gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20200716 MGI PMID:31916570 1320316 Tesmin testis expressed metallothionein like gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20220811 MGI PMID:34388164 1320316 Tesmin testis expressed metallothionein like gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220811 MGI PMID:34388164 1320319 Dock7 dedicator of cytokinesis 7 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:19202056 1320319 Dock7 dedicator of cytokinesis 7 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:19202056 1320319 Dock7 dedicator of cytokinesis 7 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:9688956 1320319 Dock7 dedicator of cytokinesis 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9688956 1320319 Dock7 dedicator of cytokinesis 7 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:19202056 1320319 Dock7 dedicator of cytokinesis 7 gene MP:0001661 extended life span IAGP N RGD:5509061 20181108 MGI PMID:760211 1320319 Dock7 dedicator of cytokinesis 7 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:9688956 1320319 Dock7 dedicator of cytokinesis 7 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:19202056 1320319 Dock7 dedicator of cytokinesis 7 gene MP:0002940 variable body spotting IEA N RGD:5509061 20111116 MGI 1320319 Dock7 dedicator of cytokinesis 7 gene MP:0005175 non-pigmented tail tip IAGP N RGD:5509061 20141003 MGI PMID:19202056 1320319 Dock7 dedicator of cytokinesis 7 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:9475748 1320319 Dock7 dedicator of cytokinesis 7 gene MP:0008779 abnormal maternal behavior IAGP N RGD:5509061 20141003 MGI PMID:19202056 1320319 Dock7 dedicator of cytokinesis 7 gene MP:0009557 decreased platelet ADP level IAGP N RGD:5509061 20141003 MGI PMID:9475748 1320319 Dock7 dedicator of cytokinesis 7 gene MP:0014168 abnormal brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:9475748 1320319 Dock7 dedicator of cytokinesis 7 gene MP:0030930 decreased digit pigmentation IAGP N RGD:5509061 20190117 MGI PMID:19202056 1320320 Sh2d7 SH2 domain containing 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1320321 Klhdc10 kelch domain containing 10 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1320321 Klhdc10 kelch domain containing 10 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1320321 Klhdc10 kelch domain containing 10 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20211014 MGI PMID:27631783 1320321 Klhdc10 kelch domain containing 10 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1320321 Klhdc10 kelch domain containing 10 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20220811 MGI 1320321 Klhdc10 kelch domain containing 10 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20211014 MGI PMID:27631783 1320321 Klhdc10 kelch domain containing 10 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20211014 MGI PMID:27631783 1320321 Klhdc10 kelch domain containing 10 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20211014 MGI PMID:27631783 1320326 Dmrta1 doublesex and mab-3 related transcription factor like family A1 gene MP:0001375 abnormal mating preference IAGP N RGD:5509061 20141003 MGI PMID:16982677 1320326 Dmrta1 doublesex and mab-3 related transcription factor like family A1 gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20141003 MGI PMID:16982677 1320326 Dmrta1 doublesex and mab-3 related transcription factor like family A1 gene MP:0031629 abnormal mounting behavior IAGP N RGD:5509061 20240704 MGI PMID:16982677 1320328 Hoxd12 homeobox D12 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:19108020 1320328 Hoxd12 homeobox D12 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:19108020 1320328 Hoxd12 homeobox D12 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:8620844 1320328 Hoxd12 homeobox D12 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:19108020 1320328 Hoxd12 homeobox D12 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8620844 1320328 Hoxd12 homeobox D12 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9659925 1320328 Hoxd12 homeobox D12 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:19108020 1320328 Hoxd12 homeobox D12 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:19108020 1320328 Hoxd12 homeobox D12 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9659925 1320328 Hoxd12 homeobox D12 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:19108020 1320328 Hoxd12 homeobox D12 gene MP:0000767 abnormal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8787740 1320328 Hoxd12 homeobox D12 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:9659925 1320328 Hoxd12 homeobox D12 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:19108020 1320328 Hoxd12 homeobox D12 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:8620844 1320328 Hoxd12 homeobox D12 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:8787740 1320328 Hoxd12 homeobox D12 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9659925 1320328 Hoxd12 homeobox D12 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:19108020 1320328 Hoxd12 homeobox D12 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:19108020 1320328 Hoxd12 homeobox D12 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:8620844 1320328 Hoxd12 homeobox D12 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:8787740 1320328 Hoxd12 homeobox D12 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:19108020 1320328 Hoxd12 homeobox D12 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:8787740 1320328 Hoxd12 homeobox D12 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:9659925 1320328 Hoxd12 homeobox D12 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:19108020 1320328 Hoxd12 homeobox D12 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9659925 1320328 Hoxd12 homeobox D12 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:8620844 1320328 Hoxd12 homeobox D12 gene MP:0004635 short metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:19108020 1320328 Hoxd12 homeobox D12 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:19108020 1320328 Hoxd12 homeobox D12 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:19108020 1320328 Hoxd12 homeobox D12 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:8787740 1320328 Hoxd12 homeobox D12 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:9521905 1320328 Hoxd12 homeobox D12 gene MP:0006253 clinodactyly IAGP N RGD:5509061 20141003 MGI PMID:19108020 1320328 Hoxd12 homeobox D12 gene MP:0009055 abnormal internal anal sphincter morphology IAGP N RGD:5509061 20141003 MGI PMID:8787740 1320328 Hoxd12 homeobox D12 gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:19108020 1320329 Apol10b apolipoprotein L 10B gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20210128 MGI 1320331 Hdac1 histone deacetylase 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20194438 1320331 Hdac1 histone deacetylase 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20571512 1320331 Hdac1 histone deacetylase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20194438 1320331 Hdac1 histone deacetylase 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0000384 distorted hair follicle pattern IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0000417 short hair IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:20194438 1320331 Hdac1 histone deacetylase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0001267 enlarged chest IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1320331 Hdac1 histone deacetylase 1 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20571512 1320331 Hdac1 histone deacetylase 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20571512 1320331 Hdac1 histone deacetylase 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:17639084 1320331 Hdac1 histone deacetylase 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:12032080 1320331 Hdac1 histone deacetylase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:19099580 1320331 Hdac1 histone deacetylase 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20194438 1320331 Hdac1 histone deacetylase 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0002015 epithelioid cyst IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20571512 1320331 Hdac1 histone deacetylase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17639084 1320331 Hdac1 histone deacetylase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19605684 1320331 Hdac1 histone deacetylase 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20571512 1320331 Hdac1 histone deacetylase 1 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20571512 1320331 Hdac1 histone deacetylase 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:20194438 1320331 Hdac1 histone deacetylase 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20571512 1320331 Hdac1 histone deacetylase 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17639084 1320331 Hdac1 histone deacetylase 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0003812 abnormal hair medulla IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0003929 decreased heart rate variability IEA N RGD:5509061 20210520 MGI 1320331 Hdac1 histone deacetylase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12032080 1320331 Hdac1 histone deacetylase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19099580 1320331 Hdac1 histone deacetylase 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0004027 trisomy IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20571512 1320331 Hdac1 histone deacetylase 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20194438 1320331 Hdac1 histone deacetylase 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20194438 1320331 Hdac1 histone deacetylase 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:20571512 1320331 Hdac1 histone deacetylase 1 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20220811 MGI 1320331 Hdac1 histone deacetylase 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1320331 Hdac1 histone deacetylase 1 gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20571512 1320331 Hdac1 histone deacetylase 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20571512 1320331 Hdac1 histone deacetylase 1 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:17639084 1320331 Hdac1 histone deacetylase 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20194438 1320331 Hdac1 histone deacetylase 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20194438 1320331 Hdac1 histone deacetylase 1 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20571512 1320331 Hdac1 histone deacetylase 1 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20194438 1320331 Hdac1 histone deacetylase 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:23287868 1320331 Hdac1 histone deacetylase 1 gene MP:0009598 thin epidermis stratum granulosum IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0010037 ectopic melanocytes IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0010683 dilated hair follicle infundibulum IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17639084 1320331 Hdac1 histone deacetylase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19099580 1320331 Hdac1 histone deacetylase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17639084 1320331 Hdac1 histone deacetylase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20194438 1320331 Hdac1 histone deacetylase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12032080 1320331 Hdac1 histone deacetylase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320331 Hdac1 histone deacetylase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12032080 1320331 Hdac1 histone deacetylase 1 gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20571512 1320331 Hdac1 histone deacetylase 1 gene MP:0012176 abnormal head development IAGP N RGD:5509061 20141003 MGI PMID:12032080 1320331 Hdac1 histone deacetylase 1 gene MP:0012404 abnormal nail color IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0012405 abnormal nail matrix morphology IAGP N RGD:5509061 20141218 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:20194438 1320331 Hdac1 histone deacetylase 1 gene MP:0013740 Meibomian gland hyperplasia IAGP N RGD:5509061 20150416 MGI PMID:23792463 1320331 Hdac1 histone deacetylase 1 gene MP:0030038 abnormal periorbital region morphology IAGP N RGD:5509061 20170914 MGI PMID:23792463 1320333 Eif4enif1 eukaryotic translation initiation factor 4E nuclear import factor 1 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20181227 MGI 1320333 Eif4enif1 eukaryotic translation initiation factor 4E nuclear import factor 1 gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 1320333 Eif4enif1 eukaryotic translation initiation factor 4E nuclear import factor 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1320333 Eif4enif1 eukaryotic translation initiation factor 4E nuclear import factor 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1320333 Eif4enif1 eukaryotic translation initiation factor 4E nuclear import factor 1 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20230601 MGI 1320333 Eif4enif1 eukaryotic translation initiation factor 4E nuclear import factor 1 gene MP:0003717 pallor IEA N RGD:5509061 20201231 MGI 1320333 Eif4enif1 eukaryotic translation initiation factor 4E nuclear import factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 1320333 Eif4enif1 eukaryotic translation initiation factor 4E nuclear import factor 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20181227 MGI 1320335 Exo5 exonuclease 5 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210729 MGI PMID:33164760 1320336 Cimap1b ciliary microtubule associated protein 1B gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20231207 MGI 1320336 Cimap1b ciliary microtubule associated protein 1B gene MP:0000274 enlarged heart IEA N RGD:5509061 20231207 MGI 1320336 Cimap1b ciliary microtubule associated protein 1B gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20231207 MGI 1320336 Cimap1b ciliary microtubule associated protein 1B gene MP:0000691 enlarged spleen IEA N RGD:5509061 20231207 MGI 1320336 Cimap1b ciliary microtubule associated protein 1B gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20231207 MGI 1320336 Cimap1b ciliary microtubule associated protein 1B gene MP:0000709 enlarged thymus IEA N RGD:5509061 20231207 MGI 1320336 Cimap1b ciliary microtubule associated protein 1B gene MP:0001262 decreased body weight IEA N RGD:5509061 20231207 MGI 1320336 Cimap1b ciliary microtubule associated protein 1B gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20231207 MGI 1320338 Rnls renalase, FAD-dependent amine oxidase gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21178975 1320338 Rnls renalase, FAD-dependent amine oxidase gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:21178975 1320338 Rnls renalase, FAD-dependent amine oxidase gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21178975 1320338 Rnls renalase, FAD-dependent amine oxidase gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:21178975 1320338 Rnls renalase, FAD-dependent amine oxidase gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21178975 1320338 Rnls renalase, FAD-dependent amine oxidase gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:21178975 1320338 Rnls renalase, FAD-dependent amine oxidase gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:21178975 1320338 Rnls renalase, FAD-dependent amine oxidase gene MP:0005662 increased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:21178975 1320338 Rnls renalase, FAD-dependent amine oxidase gene MP:0005665 increased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:21178975 1320338 Rnls renalase, FAD-dependent amine oxidase gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21178975 1320338 Rnls renalase, FAD-dependent amine oxidase gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21178975 1320340 Anln anillin, actin binding protein gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20191003 MGI PMID:30672734 1320340 Anln anillin, actin binding protein gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20241010 MGI 1320340 Anln anillin, actin binding protein gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241010 MGI 1320340 Anln anillin, actin binding protein gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20191003 MGI PMID:30672734 1320340 Anln anillin, actin binding protein gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1320340 Anln anillin, actin binding protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1320340 Anln anillin, actin binding protein gene MP:0012674 tomacula IAGP N RGD:5509061 20191003 MGI PMID:30672734 1320344 Fam13a family with sequence similarity 13, member A gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20191031 MGI PMID:29386390 1320344 Fam13a family with sequence similarity 13, member A gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180920 MGI PMID:26862784 1320344 Fam13a family with sequence similarity 13, member A gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20191031 MGI PMID:29386390 1320344 Fam13a family with sequence similarity 13, member A gene MP:0005331 insulin resistance IAGP N RGD:5509061 20191031 MGI PMID:29386390 1320344 Fam13a family with sequence similarity 13, member A gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20191031 MGI PMID:29386390 1320344 Fam13a family with sequence similarity 13, member A gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20191031 MGI PMID:29386390 1320344 Fam13a family with sequence similarity 13, member A gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20191031 MGI PMID:29386390 1320344 Fam13a family with sequence similarity 13, member A gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240321 MGI PMID:29386390 1320350 Ptpn20 protein tyrosine phosphatase, non-receptor type 20 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1320350 Ptpn20 protein tyrosine phosphatase, non-receptor type 20 gene MP:0001513 limb grasping IEA N RGD:5509061 20170105 MGI 1320350 Ptpn20 protein tyrosine phosphatase, non-receptor type 20 gene MP:0001893 non-obstructive hydrocephaly IAGP N RGD:5509061 20220714 MGI PMID:35658898 1320350 Ptpn20 protein tyrosine phosphatase, non-receptor type 20 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20230601 MGI 1320350 Ptpn20 protein tyrosine phosphatase, non-receptor type 20 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20220714 MGI PMID:35658898 1320350 Ptpn20 protein tyrosine phosphatase, non-receptor type 20 gene MP:0021024 abnormal cerebrospinal fluid physiology IAGP N RGD:5509061 20220714 MGI PMID:35658898 1320352 Sla2 Src-like-adaptor 2 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20210128 MGI 1320352 Sla2 Src-like-adaptor 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20210520 MGI 1320352 Sla2 Src-like-adaptor 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1320352 Sla2 Src-like-adaptor 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1320352 Sla2 Src-like-adaptor 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21220694 1320352 Sla2 Src-like-adaptor 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210520 MGI 1320352 Sla2 Src-like-adaptor 2 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 1320352 Sla2 Src-like-adaptor 2 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20220519 MGI 1320352 Sla2 Src-like-adaptor 2 gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21220694 1320352 Sla2 Src-like-adaptor 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21220694 1320352 Sla2 Src-like-adaptor 2 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:21220694 1320352 Sla2 Src-like-adaptor 2 gene MP:0009455 enhanced cued conditioning behavior IEA N RGD:5509061 20210128 MGI 1320355 Zfp84 zinc finger protein 84 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1320355 Zfp84 zinc finger protein 84 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210520 MGI 1320355 Zfp84 zinc finger protein 84 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1320355 Zfp84 zinc finger protein 84 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210520 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20201022 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20210128 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20180726 MGI PMID:29784826 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20201022 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20201022 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20180726 MGI PMID:29784826 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20210128 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20210520 MGI 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20180726 MGI PMID:29784826 1320356 Lrrtm2 leucine rich repeat transmembrane neuronal 2 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20180726 MGI PMID:29784826 1320358 Tmem11 transmembrane protein 11 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1320358 Tmem11 transmembrane protein 11 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20240307 MGI PMID:37286744 1320358 Tmem11 transmembrane protein 11 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20240307 MGI PMID:37286744 1320358 Tmem11 transmembrane protein 11 gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20240307 MGI PMID:37286744 1320358 Tmem11 transmembrane protein 11 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1320358 Tmem11 transmembrane protein 11 gene MP:0006321 increased myocardial fiber number IAGP N RGD:5509061 20240307 MGI PMID:37286744 1320358 Tmem11 transmembrane protein 11 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210520 MGI 1320358 Tmem11 transmembrane protein 11 gene MP:0031216 decreased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20240307 MGI PMID:37286744 1320360 Ndufa6 NADH:ubiquinone oxidoreductase subunit A6 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20220519 MGI 1320360 Ndufa6 NADH:ubiquinone oxidoreductase subunit A6 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20221215 MGI 1320360 Ndufa6 NADH:ubiquinone oxidoreductase subunit A6 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20221215 MGI 1320360 Ndufa6 NADH:ubiquinone oxidoreductase subunit A6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320360 Ndufa6 NADH:ubiquinone oxidoreductase subunit A6 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0000601 small liver IEA N RGD:5509061 20230119 MGI 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210729 MGI PMID:33631794 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20210729 MGI PMID:33631794 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:28589937 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20210729 MGI PMID:33631794 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20210729 MGI PMID:33631794 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20210729 MGI PMID:33631794 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20210729 MGI PMID:33631794 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0011637 abnormal mitochondrial matrix morphology IAGP N RGD:5509061 20210729 MGI PMID:33631794 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0014065 Lewy bodies IAGP N RGD:5509061 20210729 MGI PMID:33631794 1320362 Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20210729 MGI PMID:33631794 1320365 Myorg myogenesis regulating glycosidase (putative) gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1320370 Tecta tectorin alpha gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:24363064 1320370 Tecta tectorin alpha gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:11087000 1320370 Tecta tectorin alpha gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:15995703 1320370 Tecta tectorin alpha gene MP:0002895 abnormal otolithic membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11087000 1320370 Tecta tectorin alpha gene MP:0003143 enlarged otoliths IAGP N RGD:5509061 20141003 MGI PMID:11087000 1320370 Tecta tectorin alpha gene MP:0003144 decreased otolith number IAGP N RGD:5509061 20141003 MGI PMID:11087000 1320370 Tecta tectorin alpha gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11087000 1320370 Tecta tectorin alpha gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:15995703 1320370 Tecta tectorin alpha gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:20142329 1320370 Tecta tectorin alpha gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:24363064 1320370 Tecta tectorin alpha gene MP:0003150 detached tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:11087000 1320370 Tecta tectorin alpha gene MP:0003150 detached tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:15995703 1320370 Tecta tectorin alpha gene MP:0003150 detached tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:20142329 1320370 Tecta tectorin alpha gene MP:0004412 abnormal cochlear microphonics IAGP N RGD:5509061 20141003 MGI PMID:11087000 1320370 Tecta tectorin alpha gene MP:0004412 abnormal cochlear microphonics IAGP N RGD:5509061 20141003 MGI PMID:20142329 1320370 Tecta tectorin alpha gene MP:0004414 decreased cochlear microphonics IAGP N RGD:5509061 20141003 MGI PMID:20142329 1320370 Tecta tectorin alpha gene MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:11087000 1320370 Tecta tectorin alpha gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20141003 MGI PMID:11087000 1320370 Tecta tectorin alpha gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11087000 1320370 Tecta tectorin alpha gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20142329 1320370 Tecta tectorin alpha gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:24363064 1320370 Tecta tectorin alpha gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:20142329 1320370 Tecta tectorin alpha gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:11087000 1320370 Tecta tectorin alpha gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:14523068 1320370 Tecta tectorin alpha gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:20142329 1320370 Tecta tectorin alpha gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:20142329 1320370 Tecta tectorin alpha gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:24363064 1320370 Tecta tectorin alpha gene MP:0006336 abnormal otoacoustic response IAGP N RGD:5509061 20141003 MGI PMID:20142329 1320370 Tecta tectorin alpha gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20142329 1320370 Tecta tectorin alpha gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:24363064 1320370 Tecta tectorin alpha gene MP:0013961 abnormal Hensen stripe morphology IAGP N RGD:5509061 20160310 MGI PMID:24363064 1320370 Tecta tectorin alpha gene MP:0013962 absent Hensen stripe IAGP N RGD:5509061 20160310 MGI PMID:15995703 1320370 Tecta tectorin alpha gene MP:0014088 abnormal Kimura membrane morphology IAGP N RGD:5509061 20160421 MGI PMID:15995703 1320370 Tecta tectorin alpha gene MP:0014088 abnormal Kimura membrane morphology IAGP N RGD:5509061 20160421 MGI PMID:20142329 1320370 Tecta tectorin alpha gene MP:0014088 abnormal Kimura membrane morphology IAGP N RGD:5509061 20160421 MGI PMID:24363064 1320370 Tecta tectorin alpha gene MP:0014089 abnormal tectorial membrane marginal band morphology IAGP N RGD:5509061 20160421 MGI PMID:15995703 1320370 Tecta tectorin alpha gene MP:0014089 abnormal tectorial membrane marginal band morphology IAGP N RGD:5509061 20160421 MGI PMID:24363064 1320370 Tecta tectorin alpha gene MP:0014090 abnormal tectorial membrane covernet morphology IAGP N RGD:5509061 20160421 MGI PMID:24363064 1320370 Tecta tectorin alpha gene MP:0014091 abnormal tectorial membrane striated-sheet matrix morphology IAGP N RGD:5509061 20160421 MGI PMID:11087000 1320370 Tecta tectorin alpha gene MP:0014091 abnormal tectorial membrane striated-sheet matrix morphology IAGP N RGD:5509061 20160421 MGI PMID:15995703 1320370 Tecta tectorin alpha gene MP:0014091 abnormal tectorial membrane striated-sheet matrix morphology IAGP N RGD:5509061 20160421 MGI PMID:24363064 1320370 Tecta tectorin alpha gene MP:0014409 decreased distortion product otoacoustic emission amplitude IAGP N RGD:5509061 20240405 MGI PMID:14523068 1320376 Hoxa10 homeobox A10 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1320376 Hoxa10 homeobox A10 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1320376 Hoxa10 homeobox A10 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:12869760 1320376 Hoxa10 homeobox A10 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:7700356 1320376 Hoxa10 homeobox A10 gene MP:0000664 small prostate gland anterior lobe IAGP N RGD:5509061 20141003 MGI PMID:9915571 1320376 Hoxa10 homeobox A10 gene MP:0000665 decreased ductal branching in the coagulating gland IAGP N RGD:5509061 20141003 MGI PMID:9915571 1320376 Hoxa10 homeobox A10 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:7700356 1320376 Hoxa10 homeobox A10 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:7700356 1320376 Hoxa10 homeobox A10 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:7700356 1320376 Hoxa10 homeobox A10 gene MP:0001163 abnormal prostate gland anterior lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:9915571 1320376 Hoxa10 homeobox A10 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:7700356 1320376 Hoxa10 homeobox A10 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:7700356 1320376 Hoxa10 homeobox A10 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:7700356 1320376 Hoxa10 homeobox A10 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0002670 absent scrotum IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:9915571 1320376 Hoxa10 homeobox A10 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:17626057 1320376 Hoxa10 homeobox A10 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1320376 Hoxa10 homeobox A10 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1320376 Hoxa10 homeobox A10 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1320376 Hoxa10 homeobox A10 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:12869760 1320376 Hoxa10 homeobox A10 gene MP:0003550 short perineum IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0003854 abnormal forelimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1320376 Hoxa10 homeobox A10 gene MP:0003856 abnormal hindlimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1320376 Hoxa10 homeobox A10 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:12869760 1320376 Hoxa10 homeobox A10 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:12869760 1320376 Hoxa10 homeobox A10 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12869760 1320376 Hoxa10 homeobox A10 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12869760 1320376 Hoxa10 homeobox A10 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0004651 increased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:7700356 1320376 Hoxa10 homeobox A10 gene MP:0004654 absent lumbar vertebrae IAGP N RGD:5509061 20141003 MGI PMID:12869760 1320376 Hoxa10 homeobox A10 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0004680 small xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0004694 absent patella IAGP N RGD:5509061 20141003 MGI PMID:12869760 1320376 Hoxa10 homeobox A10 gene MP:0005149 abnormal gubernaculum morphology IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0005149 abnormal gubernaculum morphology IAGP N RGD:5509061 20141003 MGI PMID:7700356 1320376 Hoxa10 homeobox A10 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:7700356 1320376 Hoxa10 homeobox A10 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0009082 uterus cyst IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0009213 absent male inguinal canal IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0009218 absent peritoneal vaginal process IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20181227 MGI 1320376 Hoxa10 homeobox A10 gene MP:0012283 decreased sternebra number IAGP N RGD:5509061 20141003 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0013317 abnormal seminal vesicle development IAGP N RGD:5509061 20141204 MGI PMID:9915571 1320376 Hoxa10 homeobox A10 gene MP:0031286 unilateral cryptorchism IAGP N RGD:5509061 20211014 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0031287 bilateral cryptorchism IAGP N RGD:5509061 20211014 MGI PMID:7667266 1320376 Hoxa10 homeobox A10 gene MP:0031287 bilateral cryptorchism IAGP N RGD:5509061 20211014 MGI PMID:7700356 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20080989 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:20080989 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0000599 enlarged liver IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15483626 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15483626 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20080989 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15483626 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:20080989 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0003285 gastric hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15483626 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0003307 pyloric stenosis IAGP N RGD:5509061 20141003 MGI PMID:15483626 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20240523 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15483626 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:20080989 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:15483626 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1320378 Irag1 inositol 1,4,5-triphosphate receptor associated 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20231207 MGI 1320382 Limd1 LIM domains containing 1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:17092936 1320382 Limd1 LIM domains containing 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17092936 1320382 Limd1 LIM domains containing 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1320382 Limd1 LIM domains containing 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1320382 Limd1 LIM domains containing 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 1320382 Limd1 LIM domains containing 1 gene MP:0004983 abnormal osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17092936 1320382 Limd1 LIM domains containing 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1320382 Limd1 LIM domains containing 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1320382 Limd1 LIM domains containing 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 1320382 Limd1 LIM domains containing 1 gene MP:0010511 shortened PR interval IEA N RGD:5509061 20210128 MGI 1320390 Irx5 Iroquois homeobox 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:22992950 1320390 Irx5 Iroquois homeobox 5 gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20141003 MGI PMID:22992950 1320390 Irx5 Iroquois homeobox 5 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:22992950 1320390 Irx5 Iroquois homeobox 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16182275 1320390 Irx5 Iroquois homeobox 5 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:22992950 1320390 Irx5 Iroquois homeobox 5 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:22992950 1320390 Irx5 Iroquois homeobox 5 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:16182275 1320390 Irx5 Iroquois homeobox 5 gene MP:0006075 abnormal retina cone bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16182275 1320390 Irx5 Iroquois homeobox 5 gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141003 MGI PMID:22992950 1320390 Irx5 Iroquois homeobox 5 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:22992950 1320390 Irx5 Iroquois homeobox 5 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:22992950 1320390 Irx5 Iroquois homeobox 5 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:22992950 1320390 Irx5 Iroquois homeobox 5 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:22992950 1320390 Irx5 Iroquois homeobox 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22992950 1320393 Med21 mediator complex subunit 21 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10500093 1320395 Fli1 Friend leukemia integration 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:8649378 1320395 Fli1 Friend leukemia integration 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20733157 1320395 Fli1 Friend leukemia integration 1 gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20733157 1320395 Fli1 Friend leukemia integration 1 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:20733157 1320395 Fli1 Friend leukemia integration 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20733157 1320395 Fli1 Friend leukemia integration 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:10981960 1320395 Fli1 Friend leukemia integration 1 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:20733157 1320395 Fli1 Friend leukemia integration 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:10891501 1320395 Fli1 Friend leukemia integration 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:10891501 1320395 Fli1 Friend leukemia integration 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:8649378 1320395 Fli1 Friend leukemia integration 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18641300 1320395 Fli1 Friend leukemia integration 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8649378 1320395 Fli1 Friend leukemia integration 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20228226 1320395 Fli1 Friend leukemia integration 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8649378 1320395 Fli1 Friend leukemia integration 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10891501 1320395 Fli1 Friend leukemia integration 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20228226 1320395 Fli1 Friend leukemia integration 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10891501 1320395 Fli1 Friend leukemia integration 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:10891501 1320395 Fli1 Friend leukemia integration 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:18641300 1320395 Fli1 Friend leukemia integration 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20228226 1320395 Fli1 Friend leukemia integration 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10981960 1320395 Fli1 Friend leukemia integration 1 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10891501 1320395 Fli1 Friend leukemia integration 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:8649378 1320395 Fli1 Friend leukemia integration 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18641300 1320395 Fli1 Friend leukemia integration 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10981960 1320395 Fli1 Friend leukemia integration 1 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:11503960 1320395 Fli1 Friend leukemia integration 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10981960 1320395 Fli1 Friend leukemia integration 1 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:20228226 1320395 Fli1 Friend leukemia integration 1 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20733157 1320395 Fli1 Friend leukemia integration 1 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20733157 1320395 Fli1 Friend leukemia integration 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18500345 1320395 Fli1 Friend leukemia integration 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20733157 1320395 Fli1 Friend leukemia integration 1 gene MP:0003279 aneurysm IAGP N RGD:5509061 20141003 MGI PMID:20228226 1320395 Fli1 Friend leukemia integration 1 gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20228226 1320395 Fli1 Friend leukemia integration 1 gene MP:0004112 abnormal arteriole morphology IAGP N RGD:5509061 20141003 MGI PMID:20228226 1320395 Fli1 Friend leukemia integration 1 gene MP:0004125 abnormal venule morphology IAGP N RGD:5509061 20141003 MGI PMID:20228226 1320395 Fli1 Friend leukemia integration 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:18641300 1320395 Fli1 Friend leukemia integration 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18641300 1320395 Fli1 Friend leukemia integration 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18641300 1320395 Fli1 Friend leukemia integration 1 gene MP:0005412 vascular stenosis IAGP N RGD:5509061 20141003 MGI PMID:20228226 1320395 Fli1 Friend leukemia integration 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:20228226 1320395 Fli1 Friend leukemia integration 1 gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10891501 1320395 Fli1 Friend leukemia integration 1 gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:20228226 1320395 Fli1 Friend leukemia integration 1 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:20733157 1320395 Fli1 Friend leukemia integration 1 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18641300 1320395 Fli1 Friend leukemia integration 1 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18641300 1320395 Fli1 Friend leukemia integration 1 gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18641300 1320395 Fli1 Friend leukemia integration 1 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20733157 1320395 Fli1 Friend leukemia integration 1 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11503960 1320395 Fli1 Friend leukemia integration 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18641300 1320395 Fli1 Friend leukemia integration 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:18641300 1320395 Fli1 Friend leukemia integration 1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18641300 1320395 Fli1 Friend leukemia integration 1 gene MP:0009022 abnormal brain meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:10981960 1320395 Fli1 Friend leukemia integration 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20228226 1320395 Fli1 Friend leukemia integration 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20228226 1320395 Fli1 Friend leukemia integration 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10891501 1320395 Fli1 Friend leukemia integration 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10981960 1320395 Fli1 Friend leukemia integration 1 gene MP:0020326 dilated capillary IAGP N RGD:5509061 20160714 MGI PMID:20228226 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20180524 MGI PMID:29257953 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180524 MGI PMID:29257953 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0000644 dextrocardia IAGP N RGD:5509061 20180524 MGI PMID:29257953 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20180524 MGI PMID:29257953 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0000690 absent spleen IAGP N RGD:5509061 20180524 MGI PMID:29257953 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220616 MGI PMID:29733335 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220616 MGI PMID:29733335 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20220616 MGI PMID:29733335 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0002767 situs ambiguus IAGP N RGD:5509061 20180524 MGI PMID:29257953 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20210128 MGI 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20220616 MGI PMID:29733335 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220616 MGI PMID:29733335 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20180524 MGI PMID:29257953 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20210128 MGI 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0011252 situs inversus totalis IAGP N RGD:5509061 20180524 MGI PMID:29257953 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0011495 abnormal head shape IEA N RGD:5509061 20210128 MGI 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0011496 abnormal head size IEA N RGD:5509061 20210128 MGI 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220616 MGI PMID:29733335 1320398 Enkur enkurin, TRPC channel interacting protein gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220616 MGI PMID:29733335 1320400 Fgd2 FYVE, RhoGEF and PH domain containing 2 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:17234881 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20181004 MGI PMID:29859094 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0001599 abnormal blood volume IAGP N RGD:5509061 20170803 MGI PMID:28559417 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20170803 MGI PMID:28559417 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20170803 MGI PMID:28559417 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20181004 MGI PMID:29859094 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20170525 MGI PMID:28077724 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20170803 MGI PMID:28559417 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20170525 MGI PMID:28077724 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20181004 MGI PMID:29859094 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20170803 MGI PMID:28559417 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20170803 MGI PMID:28559417 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20170803 MGI PMID:28559417 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:16951310 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:16951310 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16951310 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0010170 abnormal glial cell apoptosis IAGP N RGD:5509061 20170525 MGI PMID:28077724 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20170803 MGI PMID:28559417 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0011986 decreased macrophage proliferation IAGP N RGD:5509061 20170803 MGI PMID:28559417 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0013662 decreased myeloid cell number IAGP N RGD:5509061 20181004 MGI PMID:29859094 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0020449 decreased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:28077724 1320402 Trem2 triggering receptor expressed on myeloid cells 2 gene MP:0020449 decreased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:28559417 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0000111 cleft palate IEA N RGD:5509061 20210520 MGI 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:17952091 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17952091 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17952091 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:17952091 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200402 MGI 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20181227 MGI 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20210520 MGI 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17952091 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:17952091 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20181227 MGI 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:17952091 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20181227 MGI 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20141003 MGI PMID:17952091 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:17952091 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20141003 MGI PMID:17952091 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17952091 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0011175 platyspondylia IAGP N RGD:5509061 20141003 MGI PMID:17952091 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20181227 MGI 1320405 Slc35d1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 gene MP:0030848 short ilium IAGP N RGD:5509061 20181025 MGI PMID:17952091 1320407 Pde6c phosphodiesterase 6C, cGMP specific, cone, alpha prime gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19887631 1320407 Pde6c phosphodiesterase 6C, cGMP specific, cone, alpha prime gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11853768 1320407 Pde6c phosphodiesterase 6C, cGMP specific, cone, alpha prime gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16723493 1320407 Pde6c phosphodiesterase 6C, cGMP specific, cone, alpha prime gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16723493 1320407 Pde6c phosphodiesterase 6C, cGMP specific, cone, alpha prime gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11853768 1320407 Pde6c phosphodiesterase 6C, cGMP specific, cone, alpha prime gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19887631 1320407 Pde6c phosphodiesterase 6C, cGMP specific, cone, alpha prime gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:11853768 1320407 Pde6c phosphodiesterase 6C, cGMP specific, cone, alpha prime gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:19887631 1320411 Rassf10 Ras association (RalGDS/AF-6) domain family (N-terminal) member 10 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0000962 disorganized dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0003104 acrania IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0003735 cup-shaped ears IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004282 retrognathia IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004383 absent interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004419 absent parietal bone IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004424 temporal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004475 palatine bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004570 absent glossopharyngeal nerve IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0004873 absent turbinates IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0006211 small orbits IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0006294 absent optic vesicle IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0009843 decreased neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20171019 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20171019 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20160428 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0012523 abnormal upper lip morphology IAGP N RGD:5509061 20141003 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0012706 decreased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0012757 abnormal cranial neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0012760 decreased cranial neural crest cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16938878 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0013267 first pharyngeal arch hypoplasia IAGP N RGD:5509061 20171109 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0030060 absent nasal pit IAGP N RGD:5509061 20170921 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0030084 tympanic ring hypoplasia IAGP N RGD:5509061 20170928 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0030124 middle ear ossicle hypoplasia IAGP N RGD:5509061 20171005 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0030250 frontonasal prominence hypoplasia IAGP N RGD:5509061 20171019 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0030377 zygomatic arch hypoplasia IAGP N RGD:5509061 20171207 MGI PMID:10888597 1320416 Tcof1 treacle ribosome biogenesis factor 1 gene MP:0030386 facial bone hypoplasia IAGP N RGD:5509061 20190314 MGI PMID:15042714 1320420 Hoxb2 homeobox B2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 1320420 Hoxb2 homeobox B2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0000843 absent facial nuclei IAGP N RGD:5509061 20141003 MGI PMID:10230789 1320420 Hoxb2 homeobox B2 gene MP:0000843 absent facial nuclei IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 1320420 Hoxb2 homeobox B2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:23197710 1320420 Hoxb2 homeobox B2 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:10230789 1320420 Hoxb2 homeobox B2 gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:23197710 1320420 Hoxb2 homeobox B2 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:10230789 1320420 Hoxb2 homeobox B2 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10230789 1320420 Hoxb2 homeobox B2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23197710 1320420 Hoxb2 homeobox B2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23408898 1320420 Hoxb2 homeobox B2 gene MP:0003385 abnormal body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:11518511 1320420 Hoxb2 homeobox B2 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:11518511 1320420 Hoxb2 homeobox B2 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 1320420 Hoxb2 homeobox B2 gene MP:0004561 absent facial nerve IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 1320420 Hoxb2 homeobox B2 gene MP:0009879 abnormal arcus anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0010892 increased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:23197710 1320420 Hoxb2 homeobox B2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10230789 1320420 Hoxb2 homeobox B2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10230789 1320420 Hoxb2 homeobox B2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10230789 1320420 Hoxb2 homeobox B2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23408898 1320420 Hoxb2 homeobox B2 gene MP:0012285 misaligned sternebrae IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0012490 abnormal cochlear VIII nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 1320420 Hoxb2 homeobox B2 gene MP:0012524 abnormal lower lip morphology IAGP N RGD:5509061 20141003 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0012786 increased rhombomere 1 size IAGP N RGD:5509061 20141003 MGI PMID:10230789 1320420 Hoxb2 homeobox B2 gene MP:0012796 abnormal rhombomere 4 morphology IAGP N RGD:5509061 20141003 MGI PMID:10230789 1320420 Hoxb2 homeobox B2 gene MP:0012818 rhombomere transformation IAGP N RGD:5509061 20141003 MGI PMID:10230789 1320420 Hoxb2 homeobox B2 gene MP:0030067 narrow face IAGP N RGD:5509061 20170921 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0030140 facial muscle atrophy IAGP N RGD:5509061 20171214 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0030141 facial paralysis IAGP N RGD:5509061 20171005 MGI PMID:9012503 1320420 Hoxb2 homeobox B2 gene MP:0030430 absent levator nasolabialis muscle IAGP N RGD:5509061 20171214 MGI PMID:9012503 1320423 Tbx18 T-box18 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15155583 1320423 Tbx18 T-box18 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:15155583 1320423 Tbx18 T-box18 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:15155583 1320423 Tbx18 T-box18 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16709898 1320423 Tbx18 T-box18 gene MP:0000288 abnormal pericardium morphology IAGP N RGD:5509061 20141003 MGI PMID:22926762 1320423 Tbx18 T-box18 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:20881014 1320423 Tbx18 T-box18 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:15155583 1320423 Tbx18 T-box18 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15155583 1320423 Tbx18 T-box18 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22992803 1320423 Tbx18 T-box18 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22992803 1320423 Tbx18 T-box18 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:23153495 1320423 Tbx18 T-box18 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22992803 1320423 Tbx18 T-box18 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:16709898 1320423 Tbx18 T-box18 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22926762 1320423 Tbx18 T-box18 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15155583 1320423 Tbx18 T-box18 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15155583 1320423 Tbx18 T-box18 gene MP:0003057 abnormal epicardium morphology IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0003228 abnormal sinus venosus morphology IAGP N RGD:5509061 20141003 MGI PMID:22926762 1320423 Tbx18 T-box18 gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15155583 1320423 Tbx18 T-box18 gene MP:0004682 small intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:15155583 1320423 Tbx18 T-box18 gene MP:0004682 small intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0004786 abnormal common cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:16709898 1320423 Tbx18 T-box18 gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:15155583 1320423 Tbx18 T-box18 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:15155583 1320423 Tbx18 T-box18 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22992803 1320423 Tbx18 T-box18 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15155583 1320423 Tbx18 T-box18 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:22926762 1320423 Tbx18 T-box18 gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20171026 MGI PMID:15155583 1320423 Tbx18 T-box18 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22926762 1320423 Tbx18 T-box18 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15155583 1320423 Tbx18 T-box18 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24016759 1320423 Tbx18 T-box18 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22926762 1320423 Tbx18 T-box18 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22926762 1320423 Tbx18 T-box18 gene MP:0011426 abnormal ureter smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:20881014 1320423 Tbx18 T-box18 gene MP:0012496 abnormal pleuropericardial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:22984617 1320423 Tbx18 T-box18 gene MP:0031590 abnormal epicardium development IAGP N RGD:5509061 20240229 MGI PMID:19369973 1320423 Tbx18 T-box18 gene MP:0031590 abnormal epicardium development IAGP N RGD:5509061 20240229 MGI PMID:22926762 1320424 Snx19 sorting nexin 19 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1320426 Wdr4 WD repeat domain 4 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20180215 MGI PMID:26751069 1320426 Wdr4 WD repeat domain 4 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200917 MGI PMID:26751069 1320426 Wdr4 WD repeat domain 4 gene MP:0004357 long tibia IEA N RGD:5509061 20211021 MGI 1320426 Wdr4 WD repeat domain 4 gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20180215 MGI PMID:26751069 1320426 Wdr4 WD repeat domain 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180215 MGI PMID:26751069 1320426 Wdr4 WD repeat domain 4 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20180215 MGI PMID:26751069 1320428 Ubxn2a UBX domain protein 2A gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221110 MGI 1320428 Ubxn2a UBX domain protein 2A gene MP:0001785 edema IEA N RGD:5509061 20221110 MGI 1320428 Ubxn2a UBX domain protein 2A gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20221110 MGI 1320428 Ubxn2a UBX domain protein 2A gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1320431 Adamdec1 ADAM-like, decysin 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20210318 MGI PMID:27226416 1320431 Adamdec1 ADAM-like, decysin 1 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20210318 MGI PMID:27226416 1320431 Adamdec1 ADAM-like, decysin 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20210318 MGI PMID:27226416 1320431 Adamdec1 ADAM-like, decysin 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20210318 MGI PMID:27226416 1320431 Adamdec1 ADAM-like, decysin 1 gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20210318 MGI PMID:27226416 1320431 Adamdec1 ADAM-like, decysin 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20210318 MGI PMID:27226416 1320431 Adamdec1 ADAM-like, decysin 1 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20210318 MGI PMID:27226416 1320431 Adamdec1 ADAM-like, decysin 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20210318 MGI PMID:27226416 1320431 Adamdec1 ADAM-like, decysin 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20210318 MGI PMID:27226416 1320431 Adamdec1 ADAM-like, decysin 1 gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20210318 MGI PMID:27226416 1320431 Adamdec1 ADAM-like, decysin 1 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20210318 MGI PMID:27226416 1320433 Pla2g2d phospholipase A2, group IID gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1320433 Pla2g2d phospholipase A2, group IID gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1320433 Pla2g2d phospholipase A2, group IID gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23690440 1320433 Pla2g2d phospholipase A2, group IID gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23690440 1320433 Pla2g2d phospholipase A2, group IID gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23690440 1320433 Pla2g2d phospholipase A2, group IID gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20200423 MGI PMID:26392224 1320433 Pla2g2d phospholipase A2, group IID gene MP:0005285 decreased unsaturated fatty acids level IAGP N RGD:5509061 20200423 MGI PMID:26392224 1320433 Pla2g2d phospholipase A2, group IID gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23690440 1320433 Pla2g2d phospholipase A2, group IID gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23690440 1320433 Pla2g2d phospholipase A2, group IID gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200423 MGI PMID:26392224 1320433 Pla2g2d phospholipase A2, group IID gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200423 MGI PMID:26392224 1320433 Pla2g2d phospholipase A2, group IID gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23690440 1320433 Pla2g2d phospholipase A2, group IID gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23690440 1320433 Pla2g2d phospholipase A2, group IID gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200423 MGI PMID:26392224 1320433 Pla2g2d phospholipase A2, group IID gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:23690440 1320433 Pla2g2d phospholipase A2, group IID gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20211021 MGI 1320433 Pla2g2d phospholipase A2, group IID gene MP:0020349 abnormal dendritic cell migration IAGP N RGD:5509061 20200423 MGI PMID:26392224 1320433 Pla2g2d phospholipase A2, group IID gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:26392224 1320433 Pla2g2d phospholipase A2, group IID gene MP:0031047 decreased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:26392224 1320434 Nsrp1 nuclear speckle regulatory protein 1 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20240523 MGI 1320434 Nsrp1 nuclear speckle regulatory protein 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1320434 Nsrp1 nuclear speckle regulatory protein 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20240523 MGI 1320434 Nsrp1 nuclear speckle regulatory protein 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20210930 MGI PMID:34037780 1320434 Nsrp1 nuclear speckle regulatory protein 1 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20210930 MGI PMID:34037780 1320434 Nsrp1 nuclear speckle regulatory protein 1 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20210930 MGI PMID:34037780 1320434 Nsrp1 nuclear speckle regulatory protein 1 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20210930 MGI PMID:34037780 1320434 Nsrp1 nuclear speckle regulatory protein 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20210930 MGI PMID:34037780 1320434 Nsrp1 nuclear speckle regulatory protein 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20210930 MGI PMID:34037780 1320434 Nsrp1 nuclear speckle regulatory protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21296756 1320434 Nsrp1 nuclear speckle regulatory protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1320434 Nsrp1 nuclear speckle regulatory protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20240523 MGI 1320436 Sez6 seizure related gene 6 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20170209 MGI PMID:18031681 1320436 Sez6 seizure related gene 6 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20170209 MGI PMID:18031681 1320436 Sez6 seizure related gene 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170209 MGI PMID:16814779 1320436 Sez6 seizure related gene 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170209 MGI PMID:18031681 1320436 Sez6 seizure related gene 6 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20170209 MGI PMID:18031681 1320436 Sez6 seizure related gene 6 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20170209 MGI PMID:18031681 1320436 Sez6 seizure related gene 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170209 MGI PMID:16814779 1320436 Sez6 seizure related gene 6 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20170209 MGI PMID:18031681 1320436 Sez6 seizure related gene 6 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20170209 MGI PMID:18031681 1320436 Sez6 seizure related gene 6 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20170209 MGI PMID:18031681 1320436 Sez6 seizure related gene 6 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20170209 MGI PMID:16814779 1320436 Sez6 seizure related gene 6 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20170209 MGI PMID:18031681 1320436 Sez6 seizure related gene 6 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20170209 MGI PMID:18031681 1320436 Sez6 seizure related gene 6 gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20170209 MGI PMID:16814779 1320436 Sez6 seizure related gene 6 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20170209 MGI PMID:18031681 1320436 Sez6 seizure related gene 6 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20170209 MGI PMID:18031681 1320436 Sez6 seizure related gene 6 gene MP:0011268 biphasic excitatory postsynaptic current amplitude IAGP N RGD:5509061 20170209 MGI PMID:16814779 1320436 Sez6 seizure related gene 6 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20170209 MGI PMID:16814779 1320436 Sez6 seizure related gene 6 gene MP:0011272 short excitatory postsynaptic current rise time IAGP N RGD:5509061 20170209 MGI PMID:16814779 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0008987 abnormal liver lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0009974 decreased cerebral cortex pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0011975 neuronal cytoplasmic inclusions IAGP N RGD:5509061 20141003 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:23074225 1320442 Ei24 etoposide induced 2.4 mRNA gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:23074225 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20170615 MGI PMID:26964900 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20111116 MGI 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0001136 dilated uterine cervix IEA N RGD:5509061 20111116 MGI 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0001139 abnormal vagina morphology IAGP N RGD:5509061 20170615 MGI PMID:26964900 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20170615 MGI PMID:26964900 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20170615 MGI PMID:26964900 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20170615 MGI PMID:26964900 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0001926 female infertility IEA N RGD:5509061 20111116 MGI 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0002059 abnormal seminal vesicle morphology IAGP N RGD:5509061 20170615 MGI PMID:26964900 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0002638 abnormal pupillary reflex IEA N RGD:5509061 20111116 MGI 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20170615 MGI PMID:26964900 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20170615 MGI PMID:26964900 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0003315 abnormal perineum morphology IEA N RGD:5509061 20111116 MGI 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0003531 abnormal vagina development IAGP N RGD:5509061 20170615 MGI PMID:26964900 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20170615 MGI PMID:26964900 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20170615 MGI PMID:26964900 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0008511 thin retina inner nuclear layer IEA N RGD:5509061 20111116 MGI 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0009085 abnormal uterine horn morphology IAGP N RGD:5509061 20170615 MGI PMID:26964900 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0009208 abnormal female genitalia morphology IEA N RGD:5509061 20111116 MGI 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20141003 MGI 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0013852 abnormal Mullerian duct topology IAGP N RGD:5509061 20170615 MGI PMID:26964900 1320444 Lhfpl2 lipoma HMGIC fusion partner-like 2 gene MP:0014017 abnormal Wolffian duct connection IAGP N RGD:5509061 20170615 MGI PMID:26964900 1320445 Spmip7 sperm microtubule inner protein 7 gene MP:0001147 small testis IAGP N RGD:5509061 20210506 MGI PMID:29700843 1320445 Spmip7 sperm microtubule inner protein 7 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210506 MGI PMID:29700843 1320445 Spmip7 sperm microtubule inner protein 7 gene MP:0005159 azoospermia IAGP N RGD:5509061 20210506 MGI PMID:29700843 1320446 Atl3 atlastin GTPase 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1320446 Atl3 atlastin GTPase 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1320446 Atl3 atlastin GTPase 3 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20210520 MGI 1320446 Atl3 atlastin GTPase 3 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1320446 Atl3 atlastin GTPase 3 gene MP:0004958 enlarged prostate gland IEA N RGD:5509061 20210520 MGI 1320446 Atl3 atlastin GTPase 3 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210520 MGI 1320451 Rarres2 retinoic acid receptor responder (tazarotene induced) 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22355640 1320451 Rarres2 retinoic acid receptor responder (tazarotene induced) 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:22355640 1320451 Rarres2 retinoic acid receptor responder (tazarotene induced) 2 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:22355640 1320451 Rarres2 retinoic acid receptor responder (tazarotene induced) 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:22355640 1320451 Rarres2 retinoic acid receptor responder (tazarotene induced) 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22355640 1320451 Rarres2 retinoic acid receptor responder (tazarotene induced) 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22355640 1320451 Rarres2 retinoic acid receptor responder (tazarotene induced) 2 gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:22355640 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16648486 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0003701 elevated level of mitotic sister chromatid exchange IAGP N RGD:5509061 20141003 MGI PMID:16648486 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16648486 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21390131 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16648486 1320453 Lig3 ligase III, DNA, ATP-dependent gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16648486 1320457 Maea macrophage erythroblast attacher gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:16707498 1320457 Maea macrophage erythroblast attacher gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20160421 MGI 1320457 Maea macrophage erythroblast attacher gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16707498 1320457 Maea macrophage erythroblast attacher gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16707498 1320457 Maea macrophage erythroblast attacher gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:16707498 1320457 Maea macrophage erythroblast attacher gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16707498 1320457 Maea macrophage erythroblast attacher gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16707498 1320457 Maea macrophage erythroblast attacher gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320462 Tcea1 transcription elongation factor A (SII) 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:16581793 1320462 Tcea1 transcription elongation factor A (SII) 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16581793 1320462 Tcea1 transcription elongation factor A (SII) 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:16581793 1320462 Tcea1 transcription elongation factor A (SII) 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16581793 1320462 Tcea1 transcription elongation factor A (SII) 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16581793 1320462 Tcea1 transcription elongation factor A (SII) 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:16581793 1320462 Tcea1 transcription elongation factor A (SII) 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:16581793 1320462 Tcea1 transcription elongation factor A (SII) 1 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16581793 1320462 Tcea1 transcription elongation factor A (SII) 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16581793 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22081072 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21695258 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:22081072 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22081072 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:21406566 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22081072 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22081072 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21406566 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22081072 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22081072 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:22081072 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22081072 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:21406566 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:21406566 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22081072 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:21695258 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21406566 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:21406566 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21695258 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22081072 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:20181743 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:21406566 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:21406566 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21406566 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:21406566 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0011435 increased urine magnesium level IAGP N RGD:5509061 20141003 MGI PMID:21406566 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20181743 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0011707 impaired fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:21695258 1320467 Mtss1 MTSS I-BAR domain containing 1 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:21406566 1320468 Cep57 centrosomal protein 57 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320468 Cep57 centrosomal protein 57 gene MP:0000592 short tail IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320468 Cep57 centrosomal protein 57 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320468 Cep57 centrosomal protein 57 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320468 Cep57 centrosomal protein 57 gene MP:0003051 curly tail IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320468 Cep57 centrosomal protein 57 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320468 Cep57 centrosomal protein 57 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320468 Cep57 centrosomal protein 57 gene MP:0004604 abnormal vertebral pedicle morphology IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320468 Cep57 centrosomal protein 57 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320468 Cep57 centrosomal protein 57 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320468 Cep57 centrosomal protein 57 gene MP:0005227 abnormal vertebral body development IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320468 Cep57 centrosomal protein 57 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320468 Cep57 centrosomal protein 57 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320468 Cep57 centrosomal protein 57 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320468 Cep57 centrosomal protein 57 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320468 Cep57 centrosomal protein 57 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20181108 MGI PMID:30035751 1320470 Chodl chondrolectin gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210520 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0000162 lordosis IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0000297 abnormal atrioventricular cushion morphology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0000520 absent kidney IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0000562 polydactyly IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0000632 abnormal pineal gland morphology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0000914 exencephaly IAGP N RGD:5509061 20160630 MGI PMID:27018474 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0001014 absent superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0001293 anophthalmia IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20160630 MGI PMID:27018474 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0001785 edema IAGP N RGD:5509061 20160630 MGI PMID:27018474 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160630 MGI PMID:27018474 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0002237 abnormal nasal cavity morphology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0002652 thin myocardium IAGP N RGD:5509061 20160630 MGI PMID:27018474 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0002725 abnormal vein morphology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0003078 aphakia IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0003327 liver cyst IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0003387 aorta coarctation IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0004055 heart atrium hypoplasia IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0004164 abnormal neurohypophysis morphology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20160630 MGI PMID:27018474 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20160630 MGI PMID:27018474 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0004259 small placenta IAGP N RGD:5509061 20190912 MGI PMID:29539633 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0004463 basisphenoid bone foramen IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0004612 fusion of vertebral bodies IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0005105 abnormal middle ear ossicle morphology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0005262 coloboma IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0006011 abnormal endolymphatic duct morphology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0006065 abnormal heart position or orientation IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0008922 abnormal cervical rib IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0008923 thoracoschisis IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20160630 MGI PMID:27018474 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0009770 abnormal optic chiasm morphology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0009771 absent optic chiasm IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20160630 MGI PMID:27018474 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0010490 abnormal inferior vena cava valve morphology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0010572 persistent right dorsal aorta IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0010647 heart left atrium hypoplasia IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160630 MGI PMID:27018474 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20160630 MGI PMID:27018474 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0011493 double ureter IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0011659 interrupted aortic arch, type b IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20160630 MGI PMID:27018474 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0012263 decreased hindbrain size IAGP N RGD:5509061 20160630 MGI PMID:27018474 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0013879 duplication of ductus venosus IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0013917 persistent right 6th pharyngeal arch artery IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0013970 absent connection between subcutaneous lymph vessels and lymph sac IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0020486 abnormal lens topology IEA N RGD:5509061 20180628 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0020500 persistent trigeminal artery IEA N RGD:5509061 20180628 MGI 1320474 Smg9 SMG9 nonsense mediated mRNA decay factor gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1320477 Arhgef17 Rho guanine nucleotide exchange factor 17 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20221215 MGI 1320477 Arhgef17 Rho guanine nucleotide exchange factor 17 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20190502 MGI 1320477 Arhgef17 Rho guanine nucleotide exchange factor 17 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1320479 Brd7 bromodomain containing 7 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 1320479 Brd7 bromodomain containing 7 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20141003 MGI 1320479 Brd7 bromodomain containing 7 gene MP:0000745 tremors IEA N RGD:5509061 20160804 MGI 1320479 Brd7 bromodomain containing 7 gene MP:0001147 small testis IAGP N RGD:5509061 20210923 MGI PMID:26878912 1320479 Brd7 bromodomain containing 7 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20210923 MGI PMID:26878912 1320479 Brd7 bromodomain containing 7 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20210923 MGI PMID:26878912 1320479 Brd7 bromodomain containing 7 gene MP:0001539 decreased caudal vertebrae number IEA N RGD:5509061 20160804 MGI 1320479 Brd7 bromodomain containing 7 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20161124 MGI PMID:27444544 1320479 Brd7 bromodomain containing 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20210923 MGI PMID:26878912 1320479 Brd7 bromodomain containing 7 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20160414 MGI PMID:25721744 1320479 Brd7 bromodomain containing 7 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20210923 MGI PMID:26878912 1320479 Brd7 bromodomain containing 7 gene MP:0002801 abnormal long-term object recognition memory IAGP N RGD:5509061 20160414 MGI PMID:25721744 1320479 Brd7 bromodomain containing 7 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20161124 MGI PMID:27444544 1320479 Brd7 bromodomain containing 7 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20161124 MGI PMID:27444544 1320479 Brd7 bromodomain containing 7 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210923 MGI PMID:26878912 1320479 Brd7 bromodomain containing 7 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1320479 Brd7 bromodomain containing 7 gene MP:0005159 azoospermia IAGP N RGD:5509061 20210923 MGI PMID:26878912 1320479 Brd7 bromodomain containing 7 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210923 MGI PMID:26878912 1320479 Brd7 bromodomain containing 7 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20160414 MGI PMID:25721744 1320479 Brd7 bromodomain containing 7 gene MP:0008821 increased blood uric acid level IEA N RGD:5509061 20160804 MGI 1320479 Brd7 bromodomain containing 7 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20210923 MGI PMID:26878912 1320479 Brd7 bromodomain containing 7 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20210923 MGI PMID:26878912 1320479 Brd7 bromodomain containing 7 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210923 MGI PMID:26878912 1320479 Brd7 bromodomain containing 7 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20161124 MGI PMID:27444544 1320479 Brd7 bromodomain containing 7 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20160414 MGI PMID:25721744 1320479 Brd7 bromodomain containing 7 gene MP:0012531 delayed limb development IAGP N RGD:5509061 20161124 MGI PMID:27444544 1320479 Brd7 bromodomain containing 7 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20210923 MGI PMID:26878912 1320479 Brd7 bromodomain containing 7 gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:25721744 1320483 Polh polymerase (DNA directed), eta (RAD 30 related) gene MP:0000015 abnormal ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16397220 1320483 Polh polymerase (DNA directed), eta (RAD 30 related) gene MP:0001202 skin photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:17015482 1320483 Polh polymerase (DNA directed), eta (RAD 30 related) gene MP:0001203 increased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:16397220 1320483 Polh polymerase (DNA directed), eta (RAD 30 related) gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:17015482 1320483 Polh polymerase (DNA directed), eta (RAD 30 related) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15824086 1320483 Polh polymerase (DNA directed), eta (RAD 30 related) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15939880 1320483 Polh polymerase (DNA directed), eta (RAD 30 related) gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16397220 1320483 Polh polymerase (DNA directed), eta (RAD 30 related) gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:16397220 1320483 Polh polymerase (DNA directed), eta (RAD 30 related) gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:17015482 1320483 Polh polymerase (DNA directed), eta (RAD 30 related) gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16397220 1320485 Rab6a RAB6A, member RAS oncogene family gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20171116 MGI PMID:26641717 1320485 Rab6a RAB6A, member RAS oncogene family gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20171116 MGI PMID:26304202 1320485 Rab6a RAB6A, member RAS oncogene family gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20171116 MGI PMID:26641717 1320485 Rab6a RAB6A, member RAS oncogene family gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20171116 MGI PMID:26641717 1320490 Hlcs holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1320490 Hlcs holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1320490 Hlcs holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1320490 Hlcs holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191205 MGI 1320490 Hlcs holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1320490 Hlcs holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191205 MGI 1320490 Hlcs holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1320490 Hlcs holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191205 MGI 1320490 Hlcs holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) gene MP:0009331 absent primitive node IEA N RGD:5509061 20191205 MGI 1320490 Hlcs holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1320490 Hlcs holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320490 Hlcs holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) gene MP:0012724 absent head fold IEA N RGD:5509061 20191205 MGI 1320490 Hlcs holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191205 MGI 1320492 Bdh2 3-hydroxybutyrate dehydrogenase, type 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1320494 Rad23a RAD23 homolog A, nucleotide excision repair protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12815074 1320494 Rad23a RAD23 homolog A, nucleotide excision repair protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18369441 1320494 Rad23a RAD23 homolog A, nucleotide excision repair protein gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:12815074 1320494 Rad23a RAD23 homolog A, nucleotide excision repair protein gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12815074 1320494 Rad23a RAD23 homolog A, nucleotide excision repair protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12815074 1320496 Dnajc6 DnaJ heat shock protein family (Hsp40) member C6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20160091 1320496 Dnajc6 DnaJ heat shock protein family (Hsp40) member C6 gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:20160091 1320496 Dnajc6 DnaJ heat shock protein family (Hsp40) member C6 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:20160091 1320496 Dnajc6 DnaJ heat shock protein family (Hsp40) member C6 gene MP:0008976 delayed female fertility IAGP N RGD:5509061 20141003 MGI PMID:20160091 1320496 Dnajc6 DnaJ heat shock protein family (Hsp40) member C6 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:20160091 1320496 Dnajc6 DnaJ heat shock protein family (Hsp40) member C6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20160091 1320497 Rccd1 RCC1 domain containing 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20210128 MGI 1320497 Rccd1 RCC1 domain containing 1 gene MP:0004357 long tibia IEA N RGD:5509061 20211021 MGI 1320500 Arfgef3 ARFGEF family member 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20150226 MGI PMID:24711543 1320500 Arfgef3 ARFGEF family member 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20150226 MGI PMID:24711543 1320500 Arfgef3 ARFGEF family member 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20150226 MGI PMID:24711543 1320500 Arfgef3 ARFGEF family member 3 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20150226 MGI PMID:24711543 1320500 Arfgef3 ARFGEF family member 3 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20150226 MGI PMID:24711543 1320500 Arfgef3 ARFGEF family member 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20150226 MGI PMID:24711543 1320500 Arfgef3 ARFGEF family member 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20150226 MGI PMID:24711543 1320500 Arfgef3 ARFGEF family member 3 gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:24711543 1320502 Prg3 proteoglycan 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1320502 Prg3 proteoglycan 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1320502 Prg3 proteoglycan 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1320504 Zfp105 zinc finger protein 105 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:20186958 1320504 Zfp105 zinc finger protein 105 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:20186958 1320516 Sall1 spalt like transcription factor 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19350679 1320516 Sall1 spalt like transcription factor 1 gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:16790473 1320516 Sall1 spalt like transcription factor 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:12482961 1320516 Sall1 spalt like transcription factor 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:15172686 1320516 Sall1 spalt like transcription factor 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:16790473 1320516 Sall1 spalt like transcription factor 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:19350679 1320516 Sall1 spalt like transcription factor 1 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18470945 1320516 Sall1 spalt like transcription factor 1 gene MP:0000555 absent carpal bone IAGP N RGD:5509061 20181101 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16790473 1320516 Sall1 spalt like transcription factor 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18818376 1320516 Sall1 spalt like transcription factor 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12482961 1320516 Sall1 spalt like transcription factor 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:15172686 1320516 Sall1 spalt like transcription factor 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19350679 1320516 Sall1 spalt like transcription factor 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:20127799 1320516 Sall1 spalt like transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19350679 1320516 Sall1 spalt like transcription factor 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:20127799 1320516 Sall1 spalt like transcription factor 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:12482961 1320516 Sall1 spalt like transcription factor 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:20127799 1320516 Sall1 spalt like transcription factor 1 gene MP:0003130 anal atresia IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:12482961 1320516 Sall1 spalt like transcription factor 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:16790473 1320516 Sall1 spalt like transcription factor 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12482961 1320516 Sall1 spalt like transcription factor 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:12482961 1320516 Sall1 spalt like transcription factor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18818376 1320516 Sall1 spalt like transcription factor 1 gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0004637 metacarpal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0004639 fused metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12482961 1320516 Sall1 spalt like transcription factor 1 gene MP:0005034 abnormal anus morphology IAGP N RGD:5509061 20141003 MGI PMID:16790473 1320516 Sall1 spalt like transcription factor 1 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:12482961 1320516 Sall1 spalt like transcription factor 1 gene MP:0009052 anal stenosis IAGP N RGD:5509061 20141003 MGI PMID:16790473 1320516 Sall1 spalt like transcription factor 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16790473 1320516 Sall1 spalt like transcription factor 1 gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0010985 abnormal kidney mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:20439720 1320516 Sall1 spalt like transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20127799 1320516 Sall1 spalt like transcription factor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12482961 1320516 Sall1 spalt like transcription factor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16790473 1320516 Sall1 spalt like transcription factor 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18818376 1320516 Sall1 spalt like transcription factor 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18818376 1320516 Sall1 spalt like transcription factor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11688560 1320516 Sall1 spalt like transcription factor 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12915476 1320516 Sall1 spalt like transcription factor 1 gene MP:0030862 absent triquetrum IAGP N RGD:5509061 20181101 MGI PMID:12915476 1320521 Cops6 COP9 signalosome subunit 6 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:21317535 1320521 Cops6 COP9 signalosome subunit 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21317535 1320521 Cops6 COP9 signalosome subunit 6 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:21317535 1320521 Cops6 COP9 signalosome subunit 6 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21317535 1320521 Cops6 COP9 signalosome subunit 6 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:21317535 1320521 Cops6 COP9 signalosome subunit 6 gene MP:0004503 decreased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:21317535 1320521 Cops6 COP9 signalosome subunit 6 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:21317535 1320521 Cops6 COP9 signalosome subunit 6 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21317535 1320521 Cops6 COP9 signalosome subunit 6 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21317535 1320521 Cops6 COP9 signalosome subunit 6 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20141003 MGI 1320521 Cops6 COP9 signalosome subunit 6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21317535 1320521 Cops6 COP9 signalosome subunit 6 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21317535 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:20071779 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20161103 MGI PMID:26074075 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20161103 MGI PMID:26074075 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20161103 MGI PMID:26074075 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20161103 MGI PMID:26074075 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20161103 MGI PMID:26074075 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0005283 increased unsaturated fatty acids level IAGP N RGD:5509061 20161103 MGI PMID:26074075 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20161103 MGI PMID:26074075 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20161103 MGI PMID:26074075 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20161103 MGI PMID:26074075 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20161103 MGI PMID:26074075 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20161103 MGI PMID:26074075 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20161103 MGI PMID:26074075 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20071779 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20161103 MGI PMID:26074075 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0020102 increased hepatic glucose production IAGP N RGD:5509061 20161103 MGI PMID:26074075 1320526 Ccar2 cell cycle activator and apoptosis regulator 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:20071779 1320528 Bcl11a BCL11 transcription factor A gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:23361909 1320528 Bcl11a BCL11 transcription factor A gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23576758 1320528 Bcl11a BCL11 transcription factor A gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:19657335 1320528 Bcl11a BCL11 transcription factor A gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:23361909 1320528 Bcl11a BCL11 transcription factor A gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:23230003 1320528 Bcl11a BCL11 transcription factor A gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12717432 1320528 Bcl11a BCL11 transcription factor A gene MP:0000726 absent lymphocyte IAGP N RGD:5509061 20141003 MGI PMID:24591644 1320528 Bcl11a BCL11 transcription factor A gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:22491945 1320528 Bcl11a BCL11 transcription factor A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23361909 1320528 Bcl11a BCL11 transcription factor A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23576758 1320528 Bcl11a BCL11 transcription factor A gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12717432 1320528 Bcl11a BCL11 transcription factor A gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23230003 1320528 Bcl11a BCL11 transcription factor A gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:23361909 1320528 Bcl11a BCL11 transcription factor A gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:23361909 1320528 Bcl11a BCL11 transcription factor A gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23361909 1320528 Bcl11a BCL11 transcription factor A gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23576758 1320528 Bcl11a BCL11 transcription factor A gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23361909 1320528 Bcl11a BCL11 transcription factor A gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23576758 1320528 Bcl11a BCL11 transcription factor A gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22491945 1320528 Bcl11a BCL11 transcription factor A gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:12717432 1320528 Bcl11a BCL11 transcription factor A gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23230003 1320528 Bcl11a BCL11 transcription factor A gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:24591644 1320528 Bcl11a BCL11 transcription factor A gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24591644 1320528 Bcl11a BCL11 transcription factor A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23230003 1320528 Bcl11a BCL11 transcription factor A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:24591644 1320528 Bcl11a BCL11 transcription factor A gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12717432 1320528 Bcl11a BCL11 transcription factor A gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12717432 1320528 Bcl11a BCL11 transcription factor A gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:23361909 1320528 Bcl11a BCL11 transcription factor A gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22491945 1320528 Bcl11a BCL11 transcription factor A gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:23361909 1320528 Bcl11a BCL11 transcription factor A gene MP:0005563 abnormal hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19657335 1320528 Bcl11a BCL11 transcription factor A gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:22491945 1320528 Bcl11a BCL11 transcription factor A gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:12717432 1320528 Bcl11a BCL11 transcription factor A gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:24591644 1320528 Bcl11a BCL11 transcription factor A gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12717432 1320528 Bcl11a BCL11 transcription factor A gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24591644 1320528 Bcl11a BCL11 transcription factor A gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:24591644 1320528 Bcl11a BCL11 transcription factor A gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:24591644 1320528 Bcl11a BCL11 transcription factor A gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:23230003 1320528 Bcl11a BCL11 transcription factor A gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:23230003 1320528 Bcl11a BCL11 transcription factor A gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:23230003 1320528 Bcl11a BCL11 transcription factor A gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23230003 1320528 Bcl11a BCL11 transcription factor A gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12717432 1320528 Bcl11a BCL11 transcription factor A gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:22491945 1320528 Bcl11a BCL11 transcription factor A gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:24591644 1320528 Bcl11a BCL11 transcription factor A gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:12717432 1320528 Bcl11a BCL11 transcription factor A gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23230003 1320528 Bcl11a BCL11 transcription factor A gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:22491945 1320528 Bcl11a BCL11 transcription factor A gene MP:0010132 decreased DN2 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23230003 1320528 Bcl11a BCL11 transcription factor A gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23230003 1320528 Bcl11a BCL11 transcription factor A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12717432 1320528 Bcl11a BCL11 transcription factor A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22491945 1320528 Bcl11a BCL11 transcription factor A gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:23361909 1320532 Dsg1c desmoglein 1 gamma gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210520 MGI 1320532 Dsg1c desmoglein 1 gamma gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1320532 Dsg1c desmoglein 1 gamma gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1320532 Dsg1c desmoglein 1 gamma gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1320532 Dsg1c desmoglein 1 gamma gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20210520 MGI 1320532 Dsg1c desmoglein 1 gamma gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1320532 Dsg1c desmoglein 1 gamma gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210520 MGI 1320532 Dsg1c desmoglein 1 gamma gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210520 MGI 1320532 Dsg1c desmoglein 1 gamma gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210520 MGI 1320532 Dsg1c desmoglein 1 gamma gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000160 kyphosis IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001265 decreased body size IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001265 decreased body size IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001304 cataract IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001314 cornea opacity IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001851 eye inflammation IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001924 infertility IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0002183 gliosis IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0002750 exophthalmos IAGP N RGD:5509061 20170914 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0002764 short tibia IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0003109 short femur IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0004224 absent trabecular meshwork IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0004226 absent Schlemm's canal IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0005206 abnormal aqueous humor IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0005497 optic nerve cupping IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0006120 mitral valve prolapse IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0006249 phthisis bulbi IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0009303 decreased renal fat pad weight IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0009829 enlarged eye anterior chamber IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0009829 enlarged eye anterior chamber IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0010253 posterior subcapsular cataract IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20160310 MGI PMID:25259869 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20150430 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20230810 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0013732 mature cataract IAGP N RGD:5509061 20190307 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20161027 MGI PMID:27711054 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0030030 Wormian bones IAGP N RGD:5509061 20170810 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0030852 abnormal ilium wing morphology IAGP N RGD:5509061 20181025 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0030853 abnormal iliac crest morphology IAGP N RGD:5509061 20181025 MGI PMID:20137777 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0030932 hypopyon IAGP N RGD:5509061 20190411 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0030933 hyphema IAGP N RGD:5509061 20190411 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0031213 increased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:19669234 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0031213 increased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:21282566 1320533 Sh3pxd2b SH3 and PX domains 2B gene MP:0031500 increased cornea size IAGP N RGD:5509061 20230810 MGI PMID:20137777 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23254685 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23254685 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23254685 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:23254685 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000610 cholestasis IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17360458 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:18974271 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18974271 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:17823927 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:18974271 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:17823927 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23254685 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001513 limb grasping IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23254685 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18974271 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17823927 1320535 Wwox WW domain-containing oxidoreductase gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18974271 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17823927 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17360458 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17823927 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17360458 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17823927 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002083 premature death IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141120 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:18974271 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0003017 decreased circulating bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0003103 liver degeneration IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:17823927 1320535 Wwox WW domain-containing oxidoreductase gene MP:0003354 astrocytosis IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17360458 1320535 Wwox WW domain-containing oxidoreductase gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23254685 1320535 Wwox WW domain-containing oxidoreductase gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17360458 1320535 Wwox WW domain-containing oxidoreductase gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20171221 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:18974271 1320535 Wwox WW domain-containing oxidoreductase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0005634 decreased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:18974271 1320535 Wwox WW domain-containing oxidoreductase gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17360458 1320535 Wwox WW domain-containing oxidoreductase gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17823927 1320535 Wwox WW domain-containing oxidoreductase gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0008918 microgliosis IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0008939 increased pituitary gland weight IAGP N RGD:5509061 20141120 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0009088 thin uterine horn IAGP N RGD:5509061 20141003 MGI PMID:18974271 1320535 Wwox WW domain-containing oxidoreductase gene MP:0009268 absent cerebellum fissure IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0009342 enlarged gallbladder IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0009362 abnormal primary ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18974271 1320535 Wwox WW domain-containing oxidoreductase gene MP:0009370 decreased theca cell number IAGP N RGD:5509061 20141003 MGI PMID:18974271 1320535 Wwox WW domain-containing oxidoreductase gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0009957 abnormal cerebellum vermis lobule morphology IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0010280 increased skeletal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23254685 1320535 Wwox WW domain-containing oxidoreductase gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23254685 1320535 Wwox WW domain-containing oxidoreductase gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:23254685 1320535 Wwox WW domain-containing oxidoreductase gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:23254685 1320535 Wwox WW domain-containing oxidoreductase gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:23254685 1320535 Wwox WW domain-containing oxidoreductase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19936220 1320535 Wwox WW domain-containing oxidoreductase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23254685 1320535 Wwox WW domain-containing oxidoreductase gene MP:0013307 increased adrenal gland weight IAGP N RGD:5509061 20141120 MGI PMID:18487609 1320535 Wwox WW domain-containing oxidoreductase gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320535 Wwox WW domain-containing oxidoreductase gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20231102 MGI PMID:36828035 1320541 Eya3 EYA transcriptional coactivator and phosphatase 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19102749 1320541 Eya3 EYA transcriptional coactivator and phosphatase 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19102749 1320541 Eya3 EYA transcriptional coactivator and phosphatase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19102749 1320541 Eya3 EYA transcriptional coactivator and phosphatase 3 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:19102749 1320541 Eya3 EYA transcriptional coactivator and phosphatase 3 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:19102749 1320541 Eya3 EYA transcriptional coactivator and phosphatase 3 gene MP:0005586 decreased tidal volume IAGP N RGD:5509061 20141003 MGI PMID:19102749 1320541 Eya3 EYA transcriptional coactivator and phosphatase 3 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19102749 1320541 Eya3 EYA transcriptional coactivator and phosphatase 3 gene MP:0010394 decreased QRS amplitude IAGP N RGD:5509061 20141003 MGI PMID:19102749 1320541 Eya3 EYA transcriptional coactivator and phosphatase 3 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:19102749 1320543 Gigyf1 GRB10 interacting GYF protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1320543 Gigyf1 GRB10 interacting GYF protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1320547 Ly86 lymphocyte antigen 86 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20231207 MGI 1320547 Ly86 lymphocyte antigen 86 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1320547 Ly86 lymphocyte antigen 86 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1320547 Ly86 lymphocyte antigen 86 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11861286 1320547 Ly86 lymphocyte antigen 86 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11861286 1320547 Ly86 lymphocyte antigen 86 gene MP:0002833 increased heart weight IEA N RGD:5509061 20231207 MGI 1320547 Ly86 lymphocyte antigen 86 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20231207 MGI 1320547 Ly86 lymphocyte antigen 86 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 1320547 Ly86 lymphocyte antigen 86 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11861286 1320547 Ly86 lymphocyte antigen 86 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1320547 Ly86 lymphocyte antigen 86 gene MP:0005631 decreased lung weight IEA N RGD:5509061 20231207 MGI 1320547 Ly86 lymphocyte antigen 86 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:18492657 1320547 Ly86 lymphocyte antigen 86 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:18492657 1320547 Ly86 lymphocyte antigen 86 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20231207 MGI 1320551 Cactin cactin, spliceosome C complex subunit gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1320551 Cactin cactin, spliceosome C complex subunit gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1320551 Cactin cactin, spliceosome C complex subunit gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1320551 Cactin cactin, spliceosome C complex subunit gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1320551 Cactin cactin, spliceosome C complex subunit gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1320551 Cactin cactin, spliceosome C complex subunit gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1320551 Cactin cactin, spliceosome C complex subunit gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1320551 Cactin cactin, spliceosome C complex subunit gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1320551 Cactin cactin, spliceosome C complex subunit gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1320551 Cactin cactin, spliceosome C complex subunit gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20230601 MGI 1320551 Cactin cactin, spliceosome C complex subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1320551 Cactin cactin, spliceosome C complex subunit gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20240523 MGI 1320551 Cactin cactin, spliceosome C complex subunit gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20240523 MGI 1320555 Alg2 ALG2 alpha-1,3/1,6-mannosyltransferase gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1320555 Alg2 ALG2 alpha-1,3/1,6-mannosyltransferase gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1320555 Alg2 ALG2 alpha-1,3/1,6-mannosyltransferase gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20240523 MGI 1320555 Alg2 ALG2 alpha-1,3/1,6-mannosyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1320555 Alg2 ALG2 alpha-1,3/1,6-mannosyltransferase gene MP:0011806 decreased dermal fibroblast proliferation IEA N RGD:5509061 20170406 MGI 1320555 Alg2 ALG2 alpha-1,3/1,6-mannosyltransferase gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 1320555 Alg2 ALG2 alpha-1,3/1,6-mannosyltransferase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:14695192 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:14695192 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14695192 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14695192 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14695192 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14695192 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0002039 increased neuroblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14695192 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14695192 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0003570 increased uterus leiomyoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14695192 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14695192 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14695192 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14695192 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0009311 increased duodenum adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14695192 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0009551 increased urinary bladder transitional cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14695192 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:14695192 1320557 Htatip2 HIV-1 Tat interactive protein 2 gene MP:0014127 increased thymoma incidence IAGP N RGD:5509061 20160317 MGI PMID:14695192 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:19692351 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:19692351 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19692351 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0001257 increased body length IEA N RGD:5509061 20201022 MGI 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:19692351 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19692351 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20181227 MGI 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:19692351 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:19692351 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:19692351 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:19692351 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:19692351 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:19692351 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:19692351 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19692351 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19692351 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19692351 1320559 Trpm6 transient receptor potential cation channel, subfamily M, member 6 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20210128 MGI 1320560 Rnf180 ring finger protein 180 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1320560 Rnf180 ring finger protein 180 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1320560 Rnf180 ring finger protein 180 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20170720 MGI PMID:23926250 1320560 Rnf180 ring finger protein 180 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20170720 MGI PMID:23926250 1320560 Rnf180 ring finger protein 180 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1320560 Rnf180 ring finger protein 180 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20170720 MGI PMID:23926250 1320560 Rnf180 ring finger protein 180 gene MP:0003063 increased coping response IAGP N RGD:5509061 20170720 MGI PMID:23926250 1320560 Rnf180 ring finger protein 180 gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20170720 MGI PMID:23926250 1320560 Rnf180 ring finger protein 180 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20170720 MGI PMID:23926250 1320560 Rnf180 ring finger protein 180 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20220811 MGI 1320560 Rnf180 ring finger protein 180 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1320560 Rnf180 ring finger protein 180 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20170720 MGI PMID:23926250 1320560 Rnf180 ring finger protein 180 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20170720 MGI PMID:23926250 1320560 Rnf180 ring finger protein 180 gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20170720 MGI PMID:23926250 1320561 Mul1 mitochondrial ubiquitin ligase activator of NFKB 1 gene MP:0005451 abnormal body composition IAGP N RGD:5509061 20230615 MGI PMID:28273895 1320562 Nsg2 neuron specific gene family member 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1320562 Nsg2 neuron specific gene family member 2 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20231207 MGI 1320562 Nsg2 neuron specific gene family member 2 gene MP:0009455 enhanced cued conditioning behavior IEA N RGD:5509061 20230601 MGI 1320562 Nsg2 neuron specific gene family member 2 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20231207 MGI 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0000692 small spleen IAGP N RGD:5509061 20181220 MGI PMID:30372741 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0000706 small thymus IAGP N RGD:5509061 20181220 MGI PMID:30372741 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:12915475 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:15316081 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0001306 small lens IAGP N RGD:5509061 20191219 MGI PMID:27701636 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:12915475 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17234588 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20181220 MGI PMID:30372741 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:15316081 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:22447858 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0001326 retina degeneration IAGP N RGD:5509061 20170720 MGI PMID:26978024 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:12915475 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0001999 photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:15316081 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20181220 MGI PMID:30372741 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:12915475 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20170720 MGI PMID:26978024 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0003099 retina detachment IAGP N RGD:5509061 20170720 MGI PMID:26978024 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17234588 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:12915475 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20201105 MGI PMID:32620864 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17234588 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17234588 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20181220 MGI PMID:30372741 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20181220 MGI PMID:30372741 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20191219 MGI PMID:27701636 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20181220 MGI PMID:30372741 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20181220 MGI PMID:30372741 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20170720 MGI PMID:26978024 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22447858 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20181220 MGI PMID:30372741 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0005262 coloboma IAGP N RGD:5509061 20191219 MGI PMID:27701636 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12915475 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15316081 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20181220 MGI PMID:30372741 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0008105 increased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20201105 MGI PMID:32620864 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0008452 increased retina rod cell number IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:12915475 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:17234588 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:12915475 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:12915475 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:12915475 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20181220 MGI PMID:30372741 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20240404 MGI PMID:35868845 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0010236 abnormal retina outer limiting membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12915475 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0010236 abnormal retina outer limiting membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0010236 abnormal retina outer limiting membrane morphology IAGP N RGD:5509061 20201105 MGI PMID:32620864 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17234588 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0011964 increased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20141003 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20181220 MGI PMID:30372741 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0012671 retina spots IAGP N RGD:5509061 20181220 MGI PMID:30372741 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:17234588 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0030006 decreased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:24339791 1320565 Crb1 crumbs family member 1, photoreceptor morphogenesis associated gene MP:0031220 increased circulating CXCL10 level IAGP N RGD:5509061 20240404 MGI PMID:35868845 1320566 Tmem135 transmembrane protein 135 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0005549 retina pigment epithelium hyperplasia IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0006039 decreased mitochondrial fission IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0009392 retina gliosis IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320566 Tmem135 transmembrane protein 135 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20191114 MGI PMID:27863209 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11448938 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11448938 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:16291793 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:12024028 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9784500 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:16291793 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:17356169 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:11448938 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:14982752 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:14982752 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:14982752 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18940590 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:11448938 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:14982752 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0001559 hyperglycemia IEA N RGD:5509061 20111116 MGI 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0001759 increased urine glucose level IEA N RGD:5509061 20111116 MGI 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16291793 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11448938 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11448938 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14982752 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14982752 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:18940590 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0002659 pituitary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9784500 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11448938 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11448938 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0005331 insulin resistance IEA N RGD:5509061 20111116 MGI 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:16291793 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14982752 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:11448938 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:12024028 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:14982752 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:14982752 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:14982752 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17356169 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17356169 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0006353 increased glycosylated hemoglobin level IEA N RGD:5509061 20111116 MGI 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0008845 abnormal paraventricular hypothalamic nucleus morphology IAGP N RGD:5509061 20141204 MGI PMID:9784500 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0008846 abnormal supraoptic nucleus morphology IAGP N RGD:5509061 20141204 MGI PMID:9784500 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0009468 absent magnocellular neurosecretory cells IAGP N RGD:5509061 20141204 MGI PMID:9784500 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:14982752 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9784500 1320568 Sim1 single-minded family bHLH transcription factor 1 gene MP:0013340 abnormal pituicyte morphology IAGP N RGD:5509061 20141204 MGI PMID:9784500 1320572 Paox polyamine oxidase (exo-N4-amino) gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1320572 Paox polyamine oxidase (exo-N4-amino) gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1320572 Paox polyamine oxidase (exo-N4-amino) gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1320572 Paox polyamine oxidase (exo-N4-amino) gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20211021 MGI 1320572 Paox polyamine oxidase (exo-N4-amino) gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1320572 Paox polyamine oxidase (exo-N4-amino) gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1320572 Paox polyamine oxidase (exo-N4-amino) gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1320574 Tgs1 trimethylguanosine synthase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22982455 1320574 Tgs1 trimethylguanosine synthase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:22982455 1320574 Tgs1 trimethylguanosine synthase 1 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:22982455 1320574 Tgs1 trimethylguanosine synthase 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:22982455 1320574 Tgs1 trimethylguanosine synthase 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:22982455 1320574 Tgs1 trimethylguanosine synthase 1 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:22982455 1320574 Tgs1 trimethylguanosine synthase 1 gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:22982455 1320574 Tgs1 trimethylguanosine synthase 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22982455 1320574 Tgs1 trimethylguanosine synthase 1 gene MP:0011707 impaired fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:22982455 1320586 Arrdc1 arrestin domain containing 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1320586 Arrdc1 arrestin domain containing 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1320586 Arrdc1 arrestin domain containing 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210128 MGI 1320586 Arrdc1 arrestin domain containing 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1320586 Arrdc1 arrestin domain containing 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20161208 MGI PMID:27462458 1320586 Arrdc1 arrestin domain containing 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1320588 Schip1 schwannomin interacting protein 1 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20141003 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0000445 short snout IAGP N RGD:5509061 20171019 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0000767 abnormal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19056881 1320588 Schip1 schwannomin interacting protein 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 1320588 Schip1 schwannomin interacting protein 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:19056881 1320588 Schip1 schwannomin interacting protein 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19056881 1320588 Schip1 schwannomin interacting protein 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:19056881 1320588 Schip1 schwannomin interacting protein 1 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:19056881 1320588 Schip1 schwannomin interacting protein 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 1320588 Schip1 schwannomin interacting protein 1 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:19056881 1320588 Schip1 schwannomin interacting protein 1 gene MP:0009370 decreased theca cell number IAGP N RGD:5509061 20141003 MGI PMID:19056881 1320588 Schip1 schwannomin interacting protein 1 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0009895 decreased palatine bone horizontal plate size IAGP N RGD:5509061 20141003 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:19056881 1320588 Schip1 schwannomin interacting protein 1 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0030189 broad snout IAGP N RGD:5509061 20171019 MGI PMID:17143286 1320588 Schip1 schwannomin interacting protein 1 gene MP:0030383 small presphenoid bone IAGP N RGD:5509061 20171207 MGI PMID:17143286 1320590 Cbfb core binding factor beta gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12434156 1320590 Cbfb core binding factor beta gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12434156 1320590 Cbfb core binding factor beta gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16413472 1320590 Cbfb core binding factor beta gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:16413472 1320590 Cbfb core binding factor beta gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8929537 1320590 Cbfb core binding factor beta gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:9159135 1320590 Cbfb core binding factor beta gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16413472 1320590 Cbfb core binding factor beta gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:8929537 1320590 Cbfb core binding factor beta gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:20478528 1320590 Cbfb core binding factor beta gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:8901586 1320590 Cbfb core binding factor beta gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:8929537 1320590 Cbfb core binding factor beta gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:16413472 1320590 Cbfb core binding factor beta gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16413472 1320590 Cbfb core binding factor beta gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17646405 1320590 Cbfb core binding factor beta gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20160128 MGI PMID:26418744 1320590 Cbfb core binding factor beta gene MP:0000969 abnormal nociceptor morphology IAGP N RGD:5509061 20160128 MGI PMID:26418744 1320590 Cbfb core binding factor beta gene MP:0000972 abnormal mechanoreceptor morphology IAGP N RGD:5509061 20160128 MGI PMID:26418744 1320590 Cbfb core binding factor beta gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16413472 1320590 Cbfb core binding factor beta gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16413472 1320590 Cbfb core binding factor beta gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16413472 1320590 Cbfb core binding factor beta gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23152542 1320590 Cbfb core binding factor beta gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8929537 1320590 Cbfb core binding factor beta gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8929538 1320590 Cbfb core binding factor beta gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20200514 MGI PMID:28819283 1320590 Cbfb core binding factor beta gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20478528 1320590 Cbfb core binding factor beta gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8929537 1320590 Cbfb core binding factor beta gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200514 MGI PMID:28819283 1320590 Cbfb core binding factor beta gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:8901586 1320590 Cbfb core binding factor beta gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:8929538 1320590 Cbfb core binding factor beta gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17646405 1320590 Cbfb core binding factor beta gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8929538 1320590 Cbfb core binding factor beta gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23152542 1320590 Cbfb core binding factor beta gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8901586 1320590 Cbfb core binding factor beta gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8929537 1320590 Cbfb core binding factor beta gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8929538 1320590 Cbfb core binding factor beta gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8929537 1320590 Cbfb core binding factor beta gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8929538 1320590 Cbfb core binding factor beta gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9159135 1320590 Cbfb core binding factor beta gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20160128 MGI PMID:26418744 1320590 Cbfb core binding factor beta gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8901586 1320590 Cbfb core binding factor beta gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9159135 1320590 Cbfb core binding factor beta gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17646405 1320590 Cbfb core binding factor beta gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18776905 1320590 Cbfb core binding factor beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160128 MGI PMID:26418744 1320590 Cbfb core binding factor beta gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20478528 1320590 Cbfb core binding factor beta gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17646405 1320590 Cbfb core binding factor beta gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20360383 1320590 Cbfb core binding factor beta gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:8929538 1320590 Cbfb core binding factor beta gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0002445 abnormal mononuclear cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23152542 1320590 Cbfb core binding factor beta gene MP:0002450 abnormal lymph organ development IAGP N RGD:5509061 20141003 MGI PMID:21178013 1320590 Cbfb core binding factor beta gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17646405 1320590 Cbfb core binding factor beta gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:17646405 1320590 Cbfb core binding factor beta gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:17646405 1320590 Cbfb core binding factor beta gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:12434156 1320590 Cbfb core binding factor beta gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:21178013 1320590 Cbfb core binding factor beta gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:16413472 1320590 Cbfb core binding factor beta gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9159135 1320590 Cbfb core binding factor beta gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:8929538 1320590 Cbfb core binding factor beta gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:8901586 1320590 Cbfb core binding factor beta gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20160128 MGI PMID:26418744 1320590 Cbfb core binding factor beta gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:20360383 1320590 Cbfb core binding factor beta gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20141003 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0004339 absent clavicle IAGP N RGD:5509061 20141003 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0004508 abnormal pectoral girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:16413472 1320590 Cbfb core binding factor beta gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20478528 1320590 Cbfb core binding factor beta gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17646405 1320590 Cbfb core binding factor beta gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20360383 1320590 Cbfb core binding factor beta gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200514 MGI PMID:28819283 1320590 Cbfb core binding factor beta gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20360383 1320590 Cbfb core binding factor beta gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20360383 1320590 Cbfb core binding factor beta gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:8929537 1320590 Cbfb core binding factor beta gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20160128 MGI PMID:26418744 1320590 Cbfb core binding factor beta gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:8929537 1320590 Cbfb core binding factor beta gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8929537 1320590 Cbfb core binding factor beta gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8929538 1320590 Cbfb core binding factor beta gene MP:0006051 brainstem hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8929537 1320590 Cbfb core binding factor beta gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8901586 1320590 Cbfb core binding factor beta gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8929537 1320590 Cbfb core binding factor beta gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8929538 1320590 Cbfb core binding factor beta gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9159135 1320590 Cbfb core binding factor beta gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18776905 1320590 Cbfb core binding factor beta gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20360383 1320590 Cbfb core binding factor beta gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17646405 1320590 Cbfb core binding factor beta gene MP:0008077 abnormal CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17646405 1320590 Cbfb core binding factor beta gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20360383 1320590 Cbfb core binding factor beta gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20360383 1320590 Cbfb core binding factor beta gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17646405 1320590 Cbfb core binding factor beta gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17646405 1320590 Cbfb core binding factor beta gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:21178013 1320590 Cbfb core binding factor beta gene MP:0008253 absent megakaryocytes IAGP N RGD:5509061 20141003 MGI PMID:20478528 1320590 Cbfb core binding factor beta gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0008463 abnormal peripheral lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:21178013 1320590 Cbfb core binding factor beta gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:17646405 1320590 Cbfb core binding factor beta gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20221124 MGI PMID:31171577 1320590 Cbfb core binding factor beta gene MP:0009908 protruding tongue IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23152542 1320590 Cbfb core binding factor beta gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20478528 1320590 Cbfb core binding factor beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12239155 1320590 Cbfb core binding factor beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12434156 1320590 Cbfb core binding factor beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16940420 1320590 Cbfb core binding factor beta gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16413472 1320590 Cbfb core binding factor beta gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200514 MGI PMID:28819283 1320590 Cbfb core binding factor beta gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23152542 1320590 Cbfb core binding factor beta gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8901586 1320590 Cbfb core binding factor beta gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8929537 1320590 Cbfb core binding factor beta gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8929538 1320590 Cbfb core binding factor beta gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9159135 1320590 Cbfb core binding factor beta gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20478528 1320590 Cbfb core binding factor beta gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20478528 1320590 Cbfb core binding factor beta gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:8929538 1320590 Cbfb core binding factor beta gene MP:0011615 submucous cleft palate IAGP N RGD:5509061 20221124 MGI PMID:31171577 1320590 Cbfb core binding factor beta gene MP:0011712 arrested osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:12434152 1320590 Cbfb core binding factor beta gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20200514 MGI PMID:28819283 1320590 Cbfb core binding factor beta gene MP:0014106 delayed chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:12434155 1320590 Cbfb core binding factor beta gene MP:0021214 anterior cleft palate IAGP N RGD:5509061 20221201 MGI PMID:31171577 1320594 Tbcb tubulin folding cofactor B gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241010 MGI 1320594 Tbcb tubulin folding cofactor B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1320594 Tbcb tubulin folding cofactor B gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241010 MGI 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:21075835 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:21856731 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:21856731 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0000746 weakness IAGP N RGD:5509061 20160526 MGI PMID:26385640 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20160526 MGI PMID:26385640 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21856731 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21075835 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21856731 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20160526 MGI PMID:26385640 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21856731 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0002083 premature death IAGP N RGD:5509061 20160526 MGI PMID:26385640 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21856731 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:21856731 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:21075835 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0002715 decreased glycogen catabolism rate IAGP N RGD:5509061 20141003 MGI PMID:21856731 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20160526 MGI PMID:26385640 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21075835 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21856731 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21075835 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:21075835 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0005440 increased glycogen level IAGP N RGD:5509061 20160526 MGI PMID:26385640 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21856731 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:21075835 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:21075835 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160526 MGI PMID:26385640 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20160526 MGI PMID:26385640 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:21856731 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:21856731 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:21856731 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20160526 MGI PMID:26385640 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:21856731 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:21075835 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0010580 decreased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:21075835 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21856731 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21075835 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0012051 spasticity IAGP N RGD:5509061 20160526 MGI PMID:26385640 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20160526 MGI PMID:26385640 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0014068 abnormal muscle glycogen level IAGP N RGD:5509061 20160526 MGI PMID:26385640 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0014072 decreased cardiac muscle glycogen level IAGP N RGD:5509061 20191226 MGI PMID:21075835 1320599 Gbe1 1,4-alpha-glucan branching enzyme 1 gene MP:0014074 increased brain glycogen level IAGP N RGD:5509061 20160526 MGI PMID:26385640 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0000168 abnormal bone marrow development IAGP N RGD:5509061 20141003 MGI PMID:14761685 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20211021 MGI 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:14761685 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160421 MGI 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:14761685 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:14761685 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:14761685 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:14761685 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20111116 MGI 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:14761685 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1320602 Gsta4 glutathione S-transferase, alpha 4 gene MP:0011954 shortened PQ interval IEA N RGD:5509061 20210128 MGI 1320606 Lpin3 lipin 3 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220519 MGI 1320606 Lpin3 lipin 3 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20220519 MGI 1320606 Lpin3 lipin 3 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20220519 MGI 1320606 Lpin3 lipin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191226 MGI PMID:24634820 1320606 Lpin3 lipin 3 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20230601 MGI 1320606 Lpin3 lipin 3 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20220519 MGI 1320606 Lpin3 lipin 3 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20220519 MGI 1320606 Lpin3 lipin 3 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20220519 MGI 1320606 Lpin3 lipin 3 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20191226 MGI PMID:24634820 1320606 Lpin3 lipin 3 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20191226 MGI PMID:24634820 1320606 Lpin3 lipin 3 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20191226 MGI PMID:24634820 1320606 Lpin3 lipin 3 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:24634820 1320606 Lpin3 lipin 3 gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20191226 MGI PMID:24634820 1320606 Lpin3 lipin 3 gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20191226 MGI PMID:24634820 1320608 Tlr1 toll-like receptor 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12091878 1320608 Tlr1 toll-like receptor 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12091878 1320608 Tlr1 toll-like receptor 1 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12091878 1320608 Tlr1 toll-like receptor 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:12077222 1320608 Tlr1 toll-like receptor 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:12077222 1320608 Tlr1 toll-like receptor 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:12077222 1320613 Epb41l4b erythrocyte membrane protein band 4.1 like 4b gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1320616 Pogz pogo transposable element with ZNF domain gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20191010 MGI PMID:29898395 1320616 Pogz pogo transposable element with ZNF domain gene MP:0000774 decreased brain size IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0001265 decreased body size IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0001577 anemia IAGP N RGD:5509061 20191010 MGI PMID:29898395 1320616 Pogz pogo transposable element with ZNF domain gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20191010 MGI PMID:29898395 1320616 Pogz pogo transposable element with ZNF domain gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20191010 MGI PMID:29898395 1320616 Pogz pogo transposable element with ZNF domain gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20191010 MGI PMID:29898395 1320616 Pogz pogo transposable element with ZNF domain gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20191010 MGI PMID:29898395 1320616 Pogz pogo transposable element with ZNF domain gene MP:0011275 abnormal behavioral response to light IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0014378 increased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0020507 increased dendritic spine density IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320616 Pogz pogo transposable element with ZNF domain gene MP:0020870 decreased thigmotaxis IAGP N RGD:5509061 20240404 MGI PMID:32103003 1320618 Zscan21 zinc finger and SCAN domain containing 21 gene MP:0001925 male infertility IAGP N RGD:5509061 20170720 MGI PMID:27492080 1320618 Zscan21 zinc finger and SCAN domain containing 21 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1320618 Zscan21 zinc finger and SCAN domain containing 21 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10431235 1320618 Zscan21 zinc finger and SCAN domain containing 21 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1320618 Zscan21 zinc finger and SCAN domain containing 21 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20170720 MGI PMID:27492080 1320618 Zscan21 zinc finger and SCAN domain containing 21 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20170720 MGI PMID:27492080 1320618 Zscan21 zinc finger and SCAN domain containing 21 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20170720 MGI PMID:27492080 1320618 Zscan21 zinc finger and SCAN domain containing 21 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20170720 MGI PMID:27492080 1320618 Zscan21 zinc finger and SCAN domain containing 21 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20220519 MGI 1320618 Zscan21 zinc finger and SCAN domain containing 21 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20170720 MGI PMID:27492080 1320618 Zscan21 zinc finger and SCAN domain containing 21 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1320618 Zscan21 zinc finger and SCAN domain containing 21 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20200402 MGI 1320618 Zscan21 zinc finger and SCAN domain containing 21 gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20170720 MGI PMID:27492080 1320618 Zscan21 zinc finger and SCAN domain containing 21 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1320620 Hnrnpc heterogeneous nuclear ribonucleoprotein C gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20191128 MGI 1320620 Hnrnpc heterogeneous nuclear ribonucleoprotein C gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 1320620 Hnrnpc heterogeneous nuclear ribonucleoprotein C gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:10805751 1320620 Hnrnpc heterogeneous nuclear ribonucleoprotein C gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10805751 1320620 Hnrnpc heterogeneous nuclear ribonucleoprotein C gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20181227 MGI 1320620 Hnrnpc heterogeneous nuclear ribonucleoprotein C gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 1320620 Hnrnpc heterogeneous nuclear ribonucleoprotein C gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12904583 1320620 Hnrnpc heterogeneous nuclear ribonucleoprotein C gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10805751 1320620 Hnrnpc heterogeneous nuclear ribonucleoprotein C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320620 Hnrnpc heterogeneous nuclear ribonucleoprotein C gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0001304 cataract IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0003717 pallor IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1320624 Bltp1 bridge-like lipid transfer protein family member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0000692 small spleen IEA N RGD:5509061 20210826 MGI 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12075009 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12075009 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0001922 reduced male fertility IEA N RGD:5509061 20111116 MGI 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:2346121 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0001935 decreased litter size IEA N RGD:5509061 20111116 MGI 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12075009 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:12075009 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:1759685 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:2346121 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0008545 absent sperm flagellum IEA N RGD:5509061 20111116 MGI 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:12075009 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:2346121 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20141003 MGI PMID:2346121 1320627 Hook1 hook microtubule tethering protein 1 gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20141003 MGI PMID:2346121 1320629 Sec22b SEC22 homolog B, vesicle trafficking protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220519 MGI 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20220519 MGI 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210826 MGI 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20170914 MGI PMID:28115522 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20170914 MGI PMID:28115522 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20170914 MGI PMID:28115522 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210826 MGI 1320633 Uhrf2 ubiquitin-like, containing PHD and RING finger domains 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20160421 MGI 1320635 Podn podocan gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20220811 MGI 1320635 Podn podocan gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1320635 Podn podocan gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 1320637 Nosip nitric oxide synthase interacting protein gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20240523 MGI 1320637 Nosip nitric oxide synthase interacting protein gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0000914 exencephaly IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0001293 anophthalmia IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0001297 microphthalmia IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1320637 Nosip nitric oxide synthase interacting protein gene MP:0001575 cyanosis IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20231207 MGI 1320637 Nosip nitric oxide synthase interacting protein gene MP:0001785 edema IEA N RGD:5509061 20231207 MGI 1320637 Nosip nitric oxide synthase interacting protein gene MP:0001954 respiratory distress IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20231207 MGI 1320637 Nosip nitric oxide synthase interacting protein gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0005163 cyclopia IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0005262 coloboma IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0006290 proboscis IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0008385 absent basisphenoid bone IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0010059 olfactory bulb hypoplasia IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 1320637 Nosip nitric oxide synthase interacting protein gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1320637 Nosip nitric oxide synthase interacting protein gene MP:0012683 absent telencephalon IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0030191 narrow snout IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0030268 agnathia IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320637 Nosip nitric oxide synthase interacting protein gene MP:0030558 absent nasopharynx IAGP N RGD:5509061 20210603 MGI PMID:25546391 1320642 Washc4 WASH complex subunit 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1320642 Washc4 WASH complex subunit 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20211104 MGI PMID:33749590 1320642 Washc4 WASH complex subunit 4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20211104 MGI PMID:33749590 1320642 Washc4 WASH complex subunit 4 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20211104 MGI PMID:33749590 1320642 Washc4 WASH complex subunit 4 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191128 MGI 1320642 Washc4 WASH complex subunit 4 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191128 MGI 1320642 Washc4 WASH complex subunit 4 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191128 MGI 1320642 Washc4 WASH complex subunit 4 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1320642 Washc4 WASH complex subunit 4 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20211104 MGI PMID:33749590 1320642 Washc4 WASH complex subunit 4 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191128 MGI 1320642 Washc4 WASH complex subunit 4 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20211104 MGI PMID:33749590 1320642 Washc4 WASH complex subunit 4 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20211104 MGI PMID:33749590 1320642 Washc4 WASH complex subunit 4 gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20211104 MGI PMID:33749590 1320642 Washc4 WASH complex subunit 4 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20211104 MGI PMID:33749590 1320642 Washc4 WASH complex subunit 4 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191128 MGI 1320642 Washc4 WASH complex subunit 4 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20211104 MGI PMID:33749590 1320642 Washc4 WASH complex subunit 4 gene MP:0010540 long stride length IAGP N RGD:5509061 20211104 MGI PMID:33749590 1320642 Washc4 WASH complex subunit 4 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1320642 Washc4 WASH complex subunit 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320642 Washc4 WASH complex subunit 4 gene MP:0012319 fast extinction of fear memory IAGP N RGD:5509061 20211104 MGI PMID:33749590 1320642 Washc4 WASH complex subunit 4 gene MP:0012724 absent head fold IEA N RGD:5509061 20191128 MGI 1320642 Washc4 WASH complex subunit 4 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1320642 Washc4 WASH complex subunit 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191128 MGI 1320642 Washc4 WASH complex subunit 4 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20211104 MGI PMID:33749590 1320647 Bola2 bolA family member 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201231 MGI 1320647 Bola2 bolA family member 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20170105 MGI 1320647 Bola2 bolA family member 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1320647 Bola2 bolA family member 2 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20210128 MGI 1320647 Bola2 bolA family member 2 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 1320651 Cideb cell death-inducing DNA fragmentation factor, alpha subunit-like effector B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17646209 1320651 Cideb cell death-inducing DNA fragmentation factor, alpha subunit-like effector B gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17646209 1320651 Cideb cell death-inducing DNA fragmentation factor, alpha subunit-like effector B gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17646209 1320651 Cideb cell death-inducing DNA fragmentation factor, alpha subunit-like effector B gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:17646209 1320651 Cideb cell death-inducing DNA fragmentation factor, alpha subunit-like effector B gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17646209 1320651 Cideb cell death-inducing DNA fragmentation factor, alpha subunit-like effector B gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17646209 1320651 Cideb cell death-inducing DNA fragmentation factor, alpha subunit-like effector B gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17646209 1320651 Cideb cell death-inducing DNA fragmentation factor, alpha subunit-like effector B gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17646209 1320651 Cideb cell death-inducing DNA fragmentation factor, alpha subunit-like effector B gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17646209 1320651 Cideb cell death-inducing DNA fragmentation factor, alpha subunit-like effector B gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:17646209 1320651 Cideb cell death-inducing DNA fragmentation factor, alpha subunit-like effector B gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17646209 1320651 Cideb cell death-inducing DNA fragmentation factor, alpha subunit-like effector B gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:17646209 1320651 Cideb cell death-inducing DNA fragmentation factor, alpha subunit-like effector B gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:17646209 1320653 Hoxa9 homeobox A9 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:17626057 1320653 Hoxa9 homeobox A9 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9013929 1320653 Hoxa9 homeobox A9 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17761289 1320653 Hoxa9 homeobox A9 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:8625797 1320653 Hoxa9 homeobox A9 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:9013929 1320653 Hoxa9 homeobox A9 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:9892669 1320653 Hoxa9 homeobox A9 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17761289 1320653 Hoxa9 homeobox A9 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17761289 1320653 Hoxa9 homeobox A9 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:17626057 1320653 Hoxa9 homeobox A9 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:9892669 1320653 Hoxa9 homeobox A9 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:8625797 1320653 Hoxa9 homeobox A9 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:8625797 1320653 Hoxa9 homeobox A9 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8625797 1320653 Hoxa9 homeobox A9 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:17626057 1320653 Hoxa9 homeobox A9 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1320653 Hoxa9 homeobox A9 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1320653 Hoxa9 homeobox A9 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1320653 Hoxa9 homeobox A9 gene MP:0003344 mammary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9892669 1320653 Hoxa9 homeobox A9 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1320653 Hoxa9 homeobox A9 gene MP:0004323 sternum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9013929 1320653 Hoxa9 homeobox A9 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:8625797 1320653 Hoxa9 homeobox A9 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20141003 MGI PMID:8625797 1320653 Hoxa9 homeobox A9 gene MP:0004614 caudal vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:8625797 1320653 Hoxa9 homeobox A9 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1320653 Hoxa9 homeobox A9 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:8625797 1320653 Hoxa9 homeobox A9 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:8625797 1320653 Hoxa9 homeobox A9 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1320653 Hoxa9 homeobox A9 gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1320653 Hoxa9 homeobox A9 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:8625797 1320653 Hoxa9 homeobox A9 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:17761289 1320653 Hoxa9 homeobox A9 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17761289 1320653 Hoxa9 homeobox A9 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:8625797 1320653 Hoxa9 homeobox A9 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17761289 1320653 Hoxa9 homeobox A9 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:17626057 1320653 Hoxa9 homeobox A9 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:17626057 1320658 Sbno1 strawberry notch 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20201022 MGI 1320658 Sbno1 strawberry notch 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20190103 MGI PMID:28401892 1320658 Sbno1 strawberry notch 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20181227 MGI 1320658 Sbno1 strawberry notch 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20190103 MGI PMID:28401892 1320658 Sbno1 strawberry notch 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20181227 MGI 1320658 Sbno1 strawberry notch 1 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20190103 MGI PMID:28401892 1320658 Sbno1 strawberry notch 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20190103 MGI PMID:28401892 1320658 Sbno1 strawberry notch 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1320658 Sbno1 strawberry notch 1 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1320658 Sbno1 strawberry notch 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20190103 MGI PMID:28401892 1320658 Sbno1 strawberry notch 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320658 Sbno1 strawberry notch 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1320658 Sbno1 strawberry notch 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210128 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20160804 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0000322 increased granulocyte number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20170105 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210128 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0003036 vertebral transformation IEA N RGD:5509061 20160114 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0008097 increased plasma cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0008126 increased dendritic cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0008181 increased marginal zone B cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0008211 decreased mature B cell number IEA N RGD:5509061 20160804 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0008346 increased gamma-delta T cell number IEA N RGD:5509061 20160804 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0008524 increased plasmacytoid dendritic cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20211021 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IEA N RGD:5509061 20201022 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0010851 decreased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0013418 increased memory-marker gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0013421 increased CD5-positive gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0013430 increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0013433 increased KLRG1-positive CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0013514 increased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0013651 increased CD11b-low dendritic cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0013675 decreased Ly6C-positive mature NK cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0013764 decreased T-helper cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20201231 MGI 1320659 Dph6 diphthamine biosynthesis 6 gene MP:0013775 increased KLRG1-positive T-helper cell number IEA N RGD:5509061 20201231 MGI 1320667 Mixl1 Mix paired-like homeobox gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0004838 abnormal neural fold elevation formation IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0011256 abnormal neural fold morphology IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0012081 absent heart tube IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0012086 absent hindgut IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0012183 decreased paraxial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320667 Mixl1 Mix paired-like homeobox gene MP:0012739 abnormal anterior primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:12117810 1320670 Ndufs7 NADH:ubiquinone oxidoreductase core subunit S7 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20201231 MGI 1320670 Ndufs7 NADH:ubiquinone oxidoreductase core subunit S7 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20161201 MGI 1320670 Ndufs7 NADH:ubiquinone oxidoreductase core subunit S7 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20170105 MGI 1320670 Ndufs7 NADH:ubiquinone oxidoreductase core subunit S7 gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20170105 MGI 1320670 Ndufs7 NADH:ubiquinone oxidoreductase core subunit S7 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20201231 MGI 1320670 Ndufs7 NADH:ubiquinone oxidoreductase core subunit S7 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1320670 Ndufs7 NADH:ubiquinone oxidoreductase core subunit S7 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1320670 Ndufs7 NADH:ubiquinone oxidoreductase core subunit S7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320670 Ndufs7 NADH:ubiquinone oxidoreductase core subunit S7 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1320670 Ndufs7 NADH:ubiquinone oxidoreductase core subunit S7 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1320670 Ndufs7 NADH:ubiquinone oxidoreductase core subunit S7 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1320673 Cd7 CD7 antigen gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:9637484 1320673 Cd7 CD7 antigen gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1320673 Cd7 CD7 antigen gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1320673 Cd7 CD7 antigen gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:9637484 1320673 Cd7 CD7 antigen gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9637484 1320673 Cd7 CD7 antigen gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9637484 1320677 Arhgap12 Rho GTPase activating protein 12 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1320679 Ube2h ubiquitin-conjugating enzyme E2H gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1320682 Gsx1 GS homeobox 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0001746 abnormal pituitary secretion IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0001752 abnormal hypothalamus secretion IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0002163 abnormal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0002164 abnormal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0003663 abnormal thermosensation IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0004103 abnormal ventral striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:11731457 1320682 Gsx1 GS homeobox 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0008329 decreased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0008332 decreased lactotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:11731457 1320682 Gsx1 GS homeobox 1 gene MP:0014269 decreased testes secretion IAGP N RGD:5509061 20230810 MGI PMID:8631293 1320682 Gsx1 GS homeobox 1 gene MP:0014270 decreased ovary secretion IAGP N RGD:5509061 20230810 MGI PMID:8631293 1320684 Cmtm4 CKLF-like MARVEL transmembrane domain containing 4 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20230413 MGI PMID:36271145 1320684 Cmtm4 CKLF-like MARVEL transmembrane domain containing 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20201015 MGI PMID:30867229 1320684 Cmtm4 CKLF-like MARVEL transmembrane domain containing 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20201015 MGI PMID:30867229 1320684 Cmtm4 CKLF-like MARVEL transmembrane domain containing 4 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20230413 MGI PMID:36271145 1320684 Cmtm4 CKLF-like MARVEL transmembrane domain containing 4 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20230413 MGI PMID:36271145 1320684 Cmtm4 CKLF-like MARVEL transmembrane domain containing 4 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20230413 MGI PMID:36271145 1320684 Cmtm4 CKLF-like MARVEL transmembrane domain containing 4 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20201015 MGI PMID:30867229 1320684 Cmtm4 CKLF-like MARVEL transmembrane domain containing 4 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20201015 MGI PMID:30867229 1320684 Cmtm4 CKLF-like MARVEL transmembrane domain containing 4 gene MP:0012573 decreased susceptibility to chemically induced skin inflammation IAGP N RGD:5509061 20230413 MGI PMID:36271145 1320684 Cmtm4 CKLF-like MARVEL transmembrane domain containing 4 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20230413 MGI PMID:36271145 1320684 Cmtm4 CKLF-like MARVEL transmembrane domain containing 4 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20201015 MGI PMID:30867229 1320686 Ramac RNA guanine-7 methyltransferase activating subunit gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20241003 MGI 1320686 Ramac RNA guanine-7 methyltransferase activating subunit gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20241003 MGI 1320686 Ramac RNA guanine-7 methyltransferase activating subunit gene MP:0002582 disorganized extraembryonic tissue IEA N RGD:5509061 20241003 MGI 1320686 Ramac RNA guanine-7 methyltransferase activating subunit gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20241003 MGI 1320686 Ramac RNA guanine-7 methyltransferase activating subunit gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241003 MGI 1320686 Ramac RNA guanine-7 methyltransferase activating subunit gene MP:0010052 increased grip strength IEA N RGD:5509061 20231207 MGI 1320686 Ramac RNA guanine-7 methyltransferase activating subunit gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1320686 Ramac RNA guanine-7 methyltransferase activating subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1320688 Otud6b OTU domain containing 6B gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1320688 Otud6b OTU domain containing 6B gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20170525 MGI PMID:28343629 1320688 Otud6b OTU domain containing 6B gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20170525 MGI PMID:28343629 1320688 Otud6b OTU domain containing 6B gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20170525 MGI PMID:28343629 1320688 Otud6b OTU domain containing 6B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1320691 Cstf2t cleavage stimulation factor, 3' pre-RNA subunit 2, tau gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:18077340 1320691 Cstf2t cleavage stimulation factor, 3' pre-RNA subunit 2, tau gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18077340 1320691 Cstf2t cleavage stimulation factor, 3' pre-RNA subunit 2, tau gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18077340 1320691 Cstf2t cleavage stimulation factor, 3' pre-RNA subunit 2, tau gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18077340 1320691 Cstf2t cleavage stimulation factor, 3' pre-RNA subunit 2, tau gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18077340 1320691 Cstf2t cleavage stimulation factor, 3' pre-RNA subunit 2, tau gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18077340 1320691 Cstf2t cleavage stimulation factor, 3' pre-RNA subunit 2, tau gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20141003 MGI PMID:18077340 1320691 Cstf2t cleavage stimulation factor, 3' pre-RNA subunit 2, tau gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18077340 1320691 Cstf2t cleavage stimulation factor, 3' pre-RNA subunit 2, tau gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:18077340 1320696 Sptlc3 serine palmitoyltransferase, long chain base subunit 3 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20230119 MGI 1320696 Sptlc3 serine palmitoyltransferase, long chain base subunit 3 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230119 MGI 1320696 Sptlc3 serine palmitoyltransferase, long chain base subunit 3 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1320696 Sptlc3 serine palmitoyltransferase, long chain base subunit 3 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20230119 MGI 1320699 Supt16 SPT16, facilitates chromatin remodeling subunit gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20240425 MGI PMID:36226587 1320699 Supt16 SPT16, facilitates chromatin remodeling subunit gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20240425 MGI PMID:36226587 1320699 Supt16 SPT16, facilitates chromatin remodeling subunit gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20240425 MGI PMID:36226587 1320699 Supt16 SPT16, facilitates chromatin remodeling subunit gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20240425 MGI PMID:36226587 1320699 Supt16 SPT16, facilitates chromatin remodeling subunit gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20240425 MGI PMID:36226587 1320699 Supt16 SPT16, facilitates chromatin remodeling subunit gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20240425 MGI PMID:36226587 1320699 Supt16 SPT16, facilitates chromatin remodeling subunit gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20240425 MGI PMID:36226587 1320699 Supt16 SPT16, facilitates chromatin remodeling subunit gene MP:0012204 abnormal neuronal stem cell physiology IAGP N RGD:5509061 20240425 MGI PMID:36226587 1320699 Supt16 SPT16, facilitates chromatin remodeling subunit gene MP:0012207 decreased neuronal stem cell self-renewal IAGP N RGD:5509061 20240425 MGI PMID:36226587 1320699 Supt16 SPT16, facilitates chromatin remodeling subunit gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20240425 MGI PMID:36226587 1320699 Supt16 SPT16, facilitates chromatin remodeling subunit gene MP:0014416 decreased social novelty preference IAGP N RGD:5509061 20240425 MGI PMID:36226587 1320699 Supt16 SPT16, facilitates chromatin remodeling subunit gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20240425 MGI PMID:36226587 1320699 Supt16 SPT16, facilitates chromatin remodeling subunit gene MP:0020511 decreased dendritic spine length IAGP N RGD:5509061 20240425 MGI PMID:36226587 1320699 Supt16 SPT16, facilitates chromatin remodeling subunit gene MP:0021018 decreased dendritic spine number IAGP N RGD:5509061 20240425 MGI PMID:36226587 1320699 Supt16 SPT16, facilitates chromatin remodeling subunit gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20240425 MGI PMID:36226587 1320701 Moxd1 monooxygenase, DBH-like 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1320701 Moxd1 monooxygenase, DBH-like 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20201022 MGI 1320704 Dnaja4 DnaJ heat shock protein family (Hsp40) member A4 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1320704 Dnaja4 DnaJ heat shock protein family (Hsp40) member A4 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170105 MGI 1320704 Dnaja4 DnaJ heat shock protein family (Hsp40) member A4 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210520 MGI 1320704 Dnaja4 DnaJ heat shock protein family (Hsp40) member A4 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20220519 MGI 1320704 Dnaja4 DnaJ heat shock protein family (Hsp40) member A4 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20231207 MGI 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20231207 MGI PMID:33846290 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20231109 MGI PMID:37000005 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:22723016 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:22723016 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:22723016 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22723016 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20231207 MGI PMID:33846290 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:22723016 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20231207 MGI PMID:33846290 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0005084 abnormal gallbladder morphology IAGP N RGD:5509061 20141003 MGI PMID:22723016 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20231109 MGI PMID:37000005 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20231109 MGI PMID:37000005 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20231207 MGI PMID:33846290 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:37000005 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20231207 MGI PMID:33846290 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0010414 partial atrioventricular septal defect IAGP N RGD:5509061 20231207 MGI PMID:33846290 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:37000005 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:37000005 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:37000005 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22723016 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:37000005 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20231207 MGI PMID:33846290 1320708 Sox7 SRY (sex determining region Y)-box 7 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20240125 MGI PMID:37000005 1320712 Npas1 neuronal PAS domain protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15347806 1320712 Npas1 neuronal PAS domain protein 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:15347806 1320712 Npas1 neuronal PAS domain protein 1 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:15347806 1320712 Npas1 neuronal PAS domain protein 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15347806 1320712 Npas1 neuronal PAS domain protein 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:15347806 1320712 Npas1 neuronal PAS domain protein 1 gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:15347806 1320712 Npas1 neuronal PAS domain protein 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15347806 1320712 Npas1 neuronal PAS domain protein 1 gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:15347806 1320714 Foxl2 forkhead box L2 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:15056605 1320714 Foxl2 forkhead box L2 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:20005806 1320714 Foxl2 forkhead box L2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:14736745 1320714 Foxl2 forkhead box L2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:20005806 1320714 Foxl2 forkhead box L2 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:14736745 1320714 Foxl2 forkhead box L2 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:15056605 1320714 Foxl2 forkhead box L2 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:20005806 1320714 Foxl2 forkhead box L2 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20005806 1320714 Foxl2 forkhead box L2 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:14736745 1320714 Foxl2 forkhead box L2 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:20005806 1320714 Foxl2 forkhead box L2 gene MP:0001147 small testis IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15056605 1320714 Foxl2 forkhead box L2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15056605 1320714 Foxl2 forkhead box L2 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:14736745 1320714 Foxl2 forkhead box L2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14736745 1320714 Foxl2 forkhead box L2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15056605 1320714 Foxl2 forkhead box L2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20005806 1320714 Foxl2 forkhead box L2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20005806 1320714 Foxl2 forkhead box L2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:15056605 1320714 Foxl2 forkhead box L2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1320714 Foxl2 forkhead box L2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:20005806 1320714 Foxl2 forkhead box L2 gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0003357 impaired granulosa cell differentiation IAGP N RGD:5509061 20220407 MGI PMID:14736745 1320714 Foxl2 forkhead box L2 gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:15056605 1320714 Foxl2 forkhead box L2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0004853 abnormal ovary size IAGP N RGD:5509061 20141003 MGI PMID:20005806 1320714 Foxl2 forkhead box L2 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14736745 1320714 Foxl2 forkhead box L2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15056605 1320714 Foxl2 forkhead box L2 gene MP:0011122 absent primordial ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:14736745 1320714 Foxl2 forkhead box L2 gene MP:0013395 eyelid hypoplasia IAGP N RGD:5509061 20141225 MGI PMID:15056605 1320714 Foxl2 forkhead box L2 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220630 MGI PMID:23340250 1320714 Foxl2 forkhead box L2 gene MP:0031018 decreased granulosa cell proliferation IAGP N RGD:5509061 20220407 MGI PMID:14736745 1320714 Foxl2 forkhead box L2 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:14736745 1320714 Foxl2 forkhead box L2 gene MP:0031382 absent secondary ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:14736745 1320716 Sprr1a small proline-rich protein 1A gene MP:0001314 cornea opacity IEA N RGD:5509061 20200402 MGI 1320716 Sprr1a small proline-rich protein 1A gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1320716 Sprr1a small proline-rich protein 1A gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20201231 MGI 1320716 Sprr1a small proline-rich protein 1A gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200402 MGI 1320719 Itgb3bp integrin beta 3 binding protein (beta3-endonexin) gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1320719 Itgb3bp integrin beta 3 binding protein (beta3-endonexin) gene MP:0010537 tumor regression IAGP N RGD:5509061 20230622 MGI PMID:28795467 1320719 Itgb3bp integrin beta 3 binding protein (beta3-endonexin) gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20230622 MGI PMID:28795467 1320719 Itgb3bp integrin beta 3 binding protein (beta3-endonexin) gene MP:0013151 abnormal incidence of induced tumors IAGP N RGD:5509061 20230622 MGI PMID:28795467 1320723 Adamts16 ADAM metallopeptidase with thrombospondin type 1 motif 16 gene MP:0000745 tremors IEA N RGD:5509061 20181227 MGI 1320723 Adamts16 ADAM metallopeptidase with thrombospondin type 1 motif 16 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20191205 MGI PMID:31242448 1320723 Adamts16 ADAM metallopeptidase with thrombospondin type 1 motif 16 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1320723 Adamts16 ADAM metallopeptidase with thrombospondin type 1 motif 16 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230216 MGI PMID:31748609 1320723 Adamts16 ADAM metallopeptidase with thrombospondin type 1 motif 16 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20200402 MGI 1320723 Adamts16 ADAM metallopeptidase with thrombospondin type 1 motif 16 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220519 MGI 1320723 Adamts16 ADAM metallopeptidase with thrombospondin type 1 motif 16 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220519 MGI 1320723 Adamts16 ADAM metallopeptidase with thrombospondin type 1 motif 16 gene MP:0011493 double ureter IAGP N RGD:5509061 20191205 MGI PMID:31242448 1320725 Calm4 calmodulin 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20220324 MGI PMID:25316000 1320730 Lpo lactoperoxidase gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20170105 MGI 1320730 Lpo lactoperoxidase gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0001856 myocarditis IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0001860 liver inflammation IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0001861 lung inflammation IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0001863 blood vessel inflammation IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0002064 seizures IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0002083 premature death IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0003251 gallbladder inflammation IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0003991 arteriosclerosis IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0004510 myositis IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0010138 arteritis IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0010139 aortitis IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0010861 increased respiratory mucosa goblet cell number IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0013148 mastitis IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0013485 increased Paneth cell number IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0014221 increased colon goblet cell number IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0014224 increased ileal goblet cell number IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320730 Lpo lactoperoxidase gene MP:0031118 cardiovalvulitis IAGP N RGD:5509061 20220915 MGI PMID:34127712 1320731 B4galnt4 beta-1,4-N-acetyl-galactosaminyl transferase 4 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1320731 B4galnt4 beta-1,4-N-acetyl-galactosaminyl transferase 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0000466 esophageal epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0003278 esophageal inflammation IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:17137798 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20151210 MGI PMID:24475238 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:22213801 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:22547705 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0010945 lung epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23851689 1320733 Ndfip1 Nedd4 family interacting protein 1 gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20151210 MGI PMID:24475238 1320739 Eaf1 ELL associated factor 1 gene MP:0000745 tremors IEA N RGD:5509061 20201231 MGI 1320739 Eaf1 ELL associated factor 1 gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20220303 MGI PMID:31229879 1320739 Eaf1 ELL associated factor 1 gene MP:0003608 prostate gland inflammation IAGP N RGD:5509061 20210506 MGI PMID:31229879 1320739 Eaf1 ELL associated factor 1 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20210506 MGI PMID:31229879 1320739 Eaf1 ELL associated factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320739 Eaf1 ELL associated factor 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1320741 Stx18 syntaxin 18 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1320741 Stx18 syntaxin 18 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320741 Stx18 syntaxin 18 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1320741 Stx18 syntaxin 18 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1320743 Cers2 ceramide synthase 2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19801672 1320743 Cers2 ceramide synthase 2 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19801672 1320743 Cers2 ceramide synthase 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19801672 1320743 Cers2 ceramide synthase 2 gene MP:0003005 abnormal hippocampal fimbria morphology IAGP N RGD:5509061 20141003 MGI PMID:19801672 1320743 Cers2 ceramide synthase 2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19801672 1320743 Cers2 ceramide synthase 2 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:19801672 1320743 Cers2 ceramide synthase 2 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19801672 1320743 Cers2 ceramide synthase 2 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:19801672 1320745 Myom3 myomesin family, member 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1320745 Myom3 myomesin family, member 3 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1320746 Arglu1 arginine and glutamate rich 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20220519 MGI 1320746 Arglu1 arginine and glutamate rich 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20191003 MGI PMID:30698747 1320746 Arglu1 arginine and glutamate rich 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20191003 MGI PMID:30698747 1320746 Arglu1 arginine and glutamate rich 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1320746 Arglu1 arginine and glutamate rich 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1320746 Arglu1 arginine and glutamate rich 1 gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20191003 MGI PMID:30698747 1320748 B4galt5 UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1320748 B4galt5 UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20111116 MGI 1320748 B4galt5 UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230119 MGI 1320748 B4galt5 UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19114028 1320748 B4galt5 UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1320748 B4galt5 UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230119 MGI 1320748 B4galt5 UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230119 MGI 1320748 B4galt5 UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5 gene MP:0010166 increased response to stress-induced hyperthermia IEA N RGD:5509061 20111116 MGI 1320748 B4galt5 UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19114028 1320748 B4galt5 UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1320748 B4galt5 UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 5 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20230119 MGI 1320750 Gmps guanine monophosphate synthetase gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20231207 MGI 1320750 Gmps guanine monophosphate synthetase gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20231207 MGI 1320750 Gmps guanine monophosphate synthetase gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20231207 MGI 1320750 Gmps guanine monophosphate synthetase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20240523 MGI 1320750 Gmps guanine monophosphate synthetase gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20231207 MGI 1320750 Gmps guanine monophosphate synthetase gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1320750 Gmps guanine monophosphate synthetase gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 1320750 Gmps guanine monophosphate synthetase gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1320750 Gmps guanine monophosphate synthetase gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 1320750 Gmps guanine monophosphate synthetase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1320750 Gmps guanine monophosphate synthetase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20240523 MGI 1320752 Rbks ribokinase gene MP:0003291 interstinal hyperperistalsis IAGP N RGD:5509061 20201015 MGI PMID:27194947 1320752 Rbks ribokinase gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20201015 MGI PMID:27194947 1320752 Rbks ribokinase gene MP:0011082 abnormal gastrointestinal motility IAGP N RGD:5509061 20201015 MGI PMID:27194947 1320754 Cr2 complement receptor 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11120817 1320754 Cr2 complement receptor 2 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:10779753 1320754 Cr2 complement receptor 2 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:10779753 1320754 Cr2 complement receptor 2 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:16082726 1320754 Cr2 complement receptor 2 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:8624815 1320754 Cr2 complement receptor 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:10779753 1320754 Cr2 complement receptor 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12479818 1320754 Cr2 complement receptor 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:8622941 1320754 Cr2 complement receptor 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:8624815 1320754 Cr2 complement receptor 2 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10779753 1320754 Cr2 complement receptor 2 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12479818 1320754 Cr2 complement receptor 2 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23733878 1320754 Cr2 complement receptor 2 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:8622941 1320754 Cr2 complement receptor 2 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:8624815 1320754 Cr2 complement receptor 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12479818 1320754 Cr2 complement receptor 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15585877 1320754 Cr2 complement receptor 2 gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:12479818 1320754 Cr2 complement receptor 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19706534 1320754 Cr2 complement receptor 2 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:10779753 1320754 Cr2 complement receptor 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23733878 1320754 Cr2 complement receptor 2 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11067882 1320754 Cr2 complement receptor 2 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:19706534 1320754 Cr2 complement receptor 2 gene MP:0004940 abnormal B-1 B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8624815 1320754 Cr2 complement receptor 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8624815 1320754 Cr2 complement receptor 2 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:11120817 1320754 Cr2 complement receptor 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:12165541 1320754 Cr2 complement receptor 2 gene MP:0008095 abnormal memory B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19706534 1320754 Cr2 complement receptor 2 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:10779753 1320754 Cr2 complement receptor 2 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:23733878 1320754 Cr2 complement receptor 2 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:11371362 1320754 Cr2 complement receptor 2 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:11371362 1320754 Cr2 complement receptor 2 gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23733878 1320754 Cr2 complement receptor 2 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:19706534 1320754 Cr2 complement receptor 2 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:10779753 1320754 Cr2 complement receptor 2 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:12479818 1320754 Cr2 complement receptor 2 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:8624815 1320754 Cr2 complement receptor 2 gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:8624815 1320754 Cr2 complement receptor 2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12479818 1320754 Cr2 complement receptor 2 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:8624815 1320754 Cr2 complement receptor 2 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:12479818 1320754 Cr2 complement receptor 2 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:23733878 1320754 Cr2 complement receptor 2 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:8624815 1320754 Cr2 complement receptor 2 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:12479818 1320754 Cr2 complement receptor 2 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:23733878 1320754 Cr2 complement receptor 2 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:8624815 1320754 Cr2 complement receptor 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:11120817 1320754 Cr2 complement receptor 2 gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20141003 MGI PMID:23733878 1320754 Cr2 complement receptor 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11120817 1320754 Cr2 complement receptor 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23733878 1320754 Cr2 complement receptor 2 gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20190103 MGI 1320758 Galnt14 polypeptide N-acetylgalactosaminyltransferase 14 gene MP:0003858 enhanced coordination IEA N RGD:5509061 20170406 MGI 1320762 Cops7a COP9 signalosome subunit 7A gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20231207 MGI 1320762 Cops7a COP9 signalosome subunit 7A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1320762 Cops7a COP9 signalosome subunit 7A gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1320762 Cops7a COP9 signalosome subunit 7A gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20181227 MGI 1320762 Cops7a COP9 signalosome subunit 7A gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220519 MGI 1320762 Cops7a COP9 signalosome subunit 7A gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1320762 Cops7a COP9 signalosome subunit 7A gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1320762 Cops7a COP9 signalosome subunit 7A gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1320762 Cops7a COP9 signalosome subunit 7A gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 1320762 Cops7a COP9 signalosome subunit 7A gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1320762 Cops7a COP9 signalosome subunit 7A gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20181227 MGI 1320762 Cops7a COP9 signalosome subunit 7A gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 1320762 Cops7a COP9 signalosome subunit 7A gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1320762 Cops7a COP9 signalosome subunit 7A gene MP:0009709 hydrometra IEA N RGD:5509061 20220519 MGI 1320762 Cops7a COP9 signalosome subunit 7A gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1320764 Rbm39 RNA binding motif protein 39 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12904583 1320767 Tmc2 transmembrane channel-like gene family 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22105175 1320767 Tmc2 transmembrane channel-like gene family 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:22105175 1320767 Tmc2 transmembrane channel-like gene family 2 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:22105175 1320767 Tmc2 transmembrane channel-like gene family 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:22105175 1320767 Tmc2 transmembrane channel-like gene family 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:22105175 1320767 Tmc2 transmembrane channel-like gene family 2 gene MP:0003879 abnormal hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22105175 1320767 Tmc2 transmembrane channel-like gene family 2 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22105175 1320767 Tmc2 transmembrane channel-like gene family 2 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22105175 1320767 Tmc2 transmembrane channel-like gene family 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22105175 1320767 Tmc2 transmembrane channel-like gene family 2 gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20141003 MGI PMID:22105175 1320767 Tmc2 transmembrane channel-like gene family 2 gene MP:0004432 abnormal cochlear hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22105175 1320767 Tmc2 transmembrane channel-like gene family 2 gene MP:0011039 abnormal vestibuloocular dark reflex IAGP N RGD:5509061 20141003 MGI PMID:22105175 1320767 Tmc2 transmembrane channel-like gene family 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:22105175 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20181227 MGI 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20181227 MGI 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0001199 thin skin IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0001512 trunk curl IEA N RGD:5509061 20181227 MGI 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0002607 decreased basophil cell number IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0005628 decreased circulating potassium level IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20181227 MGI 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0010205 abnormal oligodendrocyte apoptosis IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0011561 renal glomerulus lipidosis IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0011730 increased myelin sheath thickness IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20201112 MGI PMID:32330411 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0013026 decreased Ly6C low monocyte number IEA N RGD:5509061 20201022 MGI 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0013138 thin body IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1320769 Pycr2 pyrroline-5-carboxylate reductase family, member 2 gene MP:0030740 decreased circulating glutamic acid level IAGP N RGD:5509061 20240314 MGI PMID:33734376 1320771 Vnn1 vanin 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:11042271 1320775 B3gnt2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 gene MP:0001003 abnormal olfactory receptor morphology IAGP N RGD:5509061 20141003 MGI PMID:15728829 1320775 B3gnt2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20111116 MGI 1320775 B3gnt2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:15728829 1320775 B3gnt2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17890318 1320775 B3gnt2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 gene MP:0002573 behavioral despair IEA N RGD:5509061 20111116 MGI 1320775 B3gnt2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15728829 1320775 B3gnt2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17890318 1320775 B3gnt2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17890318 1320775 B3gnt2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:17890318 1320775 B3gnt2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17890318 1320775 B3gnt2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15728829 1320777 Sarm1 sterile alpha and HEAT/Armadillo motif containing 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20230914 MGI PMID:35767949 1320777 Sarm1 sterile alpha and HEAT/Armadillo motif containing 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19587044 1320777 Sarm1 sterile alpha and HEAT/Armadillo motif containing 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23499490 1320777 Sarm1 sterile alpha and HEAT/Armadillo motif containing 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:23499490 1320777 Sarm1 sterile alpha and HEAT/Armadillo motif containing 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17724133 1320777 Sarm1 sterile alpha and HEAT/Armadillo motif containing 1 gene MP:0008552 abnormal circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19587044 1320777 Sarm1 sterile alpha and HEAT/Armadillo motif containing 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20230914 MGI PMID:35767949 1320777 Sarm1 sterile alpha and HEAT/Armadillo motif containing 1 gene MP:0020449 decreased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:19587044 1320777 Sarm1 sterile alpha and HEAT/Armadillo motif containing 1 gene MP:0020943 increased susceptibility to Flaviviridae infection IAGP N RGD:5509061 20200430 MGI PMID:19587044 1320777 Sarm1 sterile alpha and HEAT/Armadillo motif containing 1 gene MP:0031044 increased susceptibility to Flaviviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:19587044 1320779 Sema3b sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15789413 1320779 Sema3b sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3B gene MP:0008228 increased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:16202709 1320781 Sdf2l1 stromal cell-derived factor 2-like 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0000111 cleft palate IEA N RGD:5509061 20221208 MGI 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20141003 MGI 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0002244 abnormal turbinate morphology IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0004017 duplex kidney IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0004320 split sternum IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0006046 atrioventricular valve regurgitation IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20231221 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0006130 pulmonary valve atresia IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0010406 common atrium IEA N RGD:5509061 20141003 MGI 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0010413 complete atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0010460 pulmonary artery hypoplasia IEA N RGD:5509061 20141003 MGI 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0011884 absent colon IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0012285 misaligned sternebrae IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0013205 abnormal nonmotile primary cilium morphology IAGP N RGD:5509061 20160519 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0021210 bilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:25877302 1320782 Cplane1 ciliogenesis and planar polarity effector 1 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:25877302 1320787 Dok4 docking protein 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1320792 Fktn fukutin gene MP:0000731 increased collagen deposition in the muscles IAGP N RGD:5509061 20141003 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:22922256 1320792 Fktn fukutin gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:22922256 1320792 Fktn fukutin gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20160114 MGI PMID:25198651 1320792 Fktn fukutin gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20160114 MGI PMID:25198651 1320792 Fktn fukutin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22922256 1320792 Fktn fukutin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15837576 1320792 Fktn fukutin gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15837576 1320792 Fktn fukutin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22922256 1320792 Fktn fukutin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:15837576 1320792 Fktn fukutin gene MP:0003044 impaired basement membrane formation IAGP N RGD:5509061 20141003 MGI PMID:15837576 1320792 Fktn fukutin gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20160114 MGI PMID:25198651 1320792 Fktn fukutin gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:15837576 1320792 Fktn fukutin gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0003954 abnormal Reichert's membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:15837576 1320792 Fktn fukutin gene MP:0004510 myositis IAGP N RGD:5509061 20160114 MGI PMID:25198651 1320792 Fktn fukutin gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17034757 1320792 Fktn fukutin gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:19017726 1320792 Fktn fukutin gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:19017726 1320792 Fktn fukutin gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20160114 MGI PMID:25198651 1320792 Fktn fukutin gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20160114 MGI PMID:25198651 1320792 Fktn fukutin gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20160114 MGI PMID:25198651 1320792 Fktn fukutin gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20160114 MGI PMID:25198651 1320792 Fktn fukutin gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:22922256 1320792 Fktn fukutin gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:22922256 1320792 Fktn fukutin gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22922256 1320792 Fktn fukutin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15837576 1320792 Fktn fukutin gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22922256 1320792 Fktn fukutin gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15837576 1320792 Fktn fukutin gene MP:0011116 absent Reichert's membrane IAGP N RGD:5509061 20141003 MGI PMID:15837576 1320792 Fktn fukutin gene MP:0011191 increased embryonic epiblast cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15837576 1320792 Fktn fukutin gene MP:0011201 abnormal visceral yolk sac cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:15837576 1320792 Fktn fukutin gene MP:0012094 abnormal Reichert's membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:15837576 1320792 Fktn fukutin gene MP:0012185 abnormal muscle precursor cell morphology IAGP N RGD:5509061 20211125 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0012186 abnormal muscle precursor cell physiology IAGP N RGD:5509061 20211125 MGI PMID:23562821 1320792 Fktn fukutin gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:23562821 1320795 Cables2 CDK5 and Abl enzyme substrate 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20210930 MGI PMID:33949947 1320795 Cables2 CDK5 and Abl enzyme substrate 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20210930 MGI PMID:33949947 1320795 Cables2 CDK5 and Abl enzyme substrate 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210930 MGI PMID:33949947 1320795 Cables2 CDK5 and Abl enzyme substrate 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20210930 MGI PMID:33949947 1320795 Cables2 CDK5 and Abl enzyme substrate 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20210930 MGI PMID:33949947 1320795 Cables2 CDK5 and Abl enzyme substrate 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20210930 MGI PMID:33949947 1320798 Wwp2 WW domain containing E3 ubiquitin protein ligase 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20160616 MGI PMID:21170031 1320798 Wwp2 WW domain containing E3 ubiquitin protein ligase 2 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20160616 MGI PMID:21170031 1320798 Wwp2 WW domain containing E3 ubiquitin protein ligase 2 gene MP:0000445 short snout IAGP N RGD:5509061 20160616 MGI PMID:21170031 1320798 Wwp2 WW domain containing E3 ubiquitin protein ligase 2 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20160616 MGI PMID:21170031 1320798 Wwp2 WW domain containing E3 ubiquitin protein ligase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160616 MGI PMID:21170031 1320798 Wwp2 WW domain containing E3 ubiquitin protein ligase 2 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20160616 MGI PMID:21170031 1320798 Wwp2 WW domain containing E3 ubiquitin protein ligase 2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20190926 MGI PMID:29695789 1320798 Wwp2 WW domain containing E3 ubiquitin protein ligase 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20160616 MGI PMID:23479606 1320798 Wwp2 WW domain containing E3 ubiquitin protein ligase 2 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20160616 MGI PMID:23479606 1320798 Wwp2 WW domain containing E3 ubiquitin protein ligase 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20160616 MGI PMID:23479606 1320798 Wwp2 WW domain containing E3 ubiquitin protein ligase 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20160616 MGI PMID:23479606 1320798 Wwp2 WW domain containing E3 ubiquitin protein ligase 2 gene MP:0030082 long lower incisors IAGP N RGD:5509061 20170928 MGI PMID:21170031 1320800 Dhx58 DExH-box helicase 58 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:20080593 1320800 Dhx58 DExH-box helicase 58 gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:20080593 1320800 Dhx58 DExH-box helicase 58 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22841161 1320800 Dhx58 DExH-box helicase 58 gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20141003 MGI PMID:17475874 1320800 Dhx58 DExH-box helicase 58 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22841161 1320800 Dhx58 DExH-box helicase 58 gene MP:0008562 increased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:17475874 1320800 Dhx58 DExH-box helicase 58 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:17475874 1320800 Dhx58 DExH-box helicase 58 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:17475874 1320800 Dhx58 DExH-box helicase 58 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:17475874 1320800 Dhx58 DExH-box helicase 58 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20080593 1320800 Dhx58 DExH-box helicase 58 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22841161 1320800 Dhx58 DExH-box helicase 58 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22841161 1320800 Dhx58 DExH-box helicase 58 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20141003 MGI PMID:20080593 1320800 Dhx58 DExH-box helicase 58 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:17475874 1320800 Dhx58 DExH-box helicase 58 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:17475874 1320800 Dhx58 DExH-box helicase 58 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20080593 1320800 Dhx58 DExH-box helicase 58 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1320800 Dhx58 DExH-box helicase 58 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17475874 1320800 Dhx58 DExH-box helicase 58 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17475874 1320800 Dhx58 DExH-box helicase 58 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20080593 1320800 Dhx58 DExH-box helicase 58 gene MP:0020912 abnormal susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:17475874 1320800 Dhx58 DExH-box helicase 58 gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:17475874 1320800 Dhx58 DExH-box helicase 58 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:17475874 1320800 Dhx58 DExH-box helicase 58 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:20080593 1320800 Dhx58 DExH-box helicase 58 gene MP:0020943 increased susceptibility to Flaviviridae infection IAGP N RGD:5509061 20200430 MGI PMID:22841161 1320800 Dhx58 DExH-box helicase 58 gene MP:0031040 increased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:20080593 1320800 Dhx58 DExH-box helicase 58 gene MP:0031044 increased susceptibility to Flaviviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:22841161 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20160804 MGI 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0000414 alopecia IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0000416 sparse hair IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0000648 absent sebaceous gland IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0001192 scaly skin IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0001193 psoriasis IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0001194 dermatitis IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0001212 skin lesions IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0001874 acanthosis IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0002074 abnormal hair texture IEA N RGD:5509061 20141003 MGI 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20141003 MGI 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0003853 dry skin IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20141003 MGI 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20160804 MGI 1320804 Arpc4 actin related protein 2/3 complex, subunit 4 gene MP:0030529 abnormal head skin morphology IAGP N RGD:5509061 20180222 MGI PMID:29113991 1320806 Rnf111 ring finger 111 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:11298452 1320806 Rnf111 ring finger 111 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11298452 1320806 Rnf111 ring finger 111 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11298452 1320806 Rnf111 ring finger 111 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11298452 1320806 Rnf111 ring finger 111 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11298452 1320808 Tpd52l1 tumor protein D52-like 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1320815 Hnf4g hepatocyte nuclear factor 4, gamma gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16945327 1320815 Hnf4g hepatocyte nuclear factor 4, gamma gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:16945327 1320815 Hnf4g hepatocyte nuclear factor 4, gamma gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:16945327 1320815 Hnf4g hepatocyte nuclear factor 4, gamma gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1320815 Hnf4g hepatocyte nuclear factor 4, gamma gene MP:0002989 small kidney IEA N RGD:5509061 20201022 MGI 1320815 Hnf4g hepatocyte nuclear factor 4, gamma gene MP:0003064 decreased coping response IAGP N RGD:5509061 20141003 MGI PMID:16945327 1320815 Hnf4g hepatocyte nuclear factor 4, gamma gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16945327 1320815 Hnf4g hepatocyte nuclear factor 4, gamma gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1320815 Hnf4g hepatocyte nuclear factor 4, gamma gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:16945327 1320815 Hnf4g hepatocyte nuclear factor 4, gamma gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:16945327 1320815 Hnf4g hepatocyte nuclear factor 4, gamma gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:16945327 1320817 Ttyh1 tweety family member 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:20568244 1320817 Ttyh1 tweety family member 1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:20568244 1320817 Ttyh1 tweety family member 1 gene MP:0003707 increased cell nucleus count IAGP N RGD:5509061 20141003 MGI PMID:20568244 1320817 Ttyh1 tweety family member 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20568244 1320817 Ttyh1 tweety family member 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20568244 1320817 Ttyh1 tweety family member 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 1320819 Ddx20 DEAD box helicase 20 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20170209 MGI PMID:18258677 1320819 Ddx20 DEAD box helicase 20 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20170209 MGI PMID:18258677 1320819 Ddx20 DEAD box helicase 20 gene MP:0002664 decreased circulating adrenocorticotropin level IAGP N RGD:5509061 20170209 MGI PMID:18258677 1320819 Ddx20 DEAD box helicase 20 gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20170209 MGI PMID:18258677 1320819 Ddx20 DEAD box helicase 20 gene MP:0004855 increased ovary weight IAGP N RGD:5509061 20170209 MGI PMID:18258677 1320819 Ddx20 DEAD box helicase 20 gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20170209 MGI PMID:18258677 1320819 Ddx20 DEAD box helicase 20 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:18258677 1320821 Trim27 tripartite motif-containing 27 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22556269 1320821 Trim27 tripartite motif-containing 27 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22556269 1320821 Trim27 tripartite motif-containing 27 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:24144979 1320821 Trim27 tripartite motif-containing 27 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22556269 1320821 Trim27 tripartite motif-containing 27 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22556269 1320821 Trim27 tripartite motif-containing 27 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:22128329 1320821 Trim27 tripartite motif-containing 27 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:22128329 1320821 Trim27 tripartite motif-containing 27 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:24144979 1320821 Trim27 tripartite motif-containing 27 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:22556269 1320821 Trim27 tripartite motif-containing 27 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22128329 1320821 Trim27 tripartite motif-containing 27 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22128329 1320821 Trim27 tripartite motif-containing 27 gene MP:0008891 decreased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24144979 1320821 Trim27 tripartite motif-containing 27 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:24144979 1320821 Trim27 tripartite motif-containing 27 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:24144979 1320821 Trim27 tripartite motif-containing 27 gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22556269 1320821 Trim27 tripartite motif-containing 27 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22556269 1320825 Armh4 armadillo-like helical domain containing 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1320825 Armh4 armadillo-like helical domain containing 4 gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 1320825 Armh4 armadillo-like helical domain containing 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0002732 increased trichoepithelioma incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20211021 MGI 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320829 Tnk1 tyrosine kinase, non-receptor, 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18974114 1320831 Mtap methylthioadenosine phosphorylase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17534888 1320831 Mtap methylthioadenosine phosphorylase gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210520 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210520 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20220519 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0001726 abnormal allantois morphology IEA N RGD:5509061 20210128 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:17534888 1320831 Mtap methylthioadenosine phosphorylase gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0002824 abnormal chorioallantoic fusion IEA N RGD:5509061 20210128 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20220519 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1320831 Mtap methylthioadenosine phosphorylase gene MP:0010138 arteritis IAGP N RGD:5509061 20141003 MGI PMID:17534888 1320831 Mtap methylthioadenosine phosphorylase gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17534888 1320831 Mtap methylthioadenosine phosphorylase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320833 Tnfrsf14 tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator) gene MP:0001993 abnormal blinking IAGP N RGD:5509061 20170921 MGI PMID:28114589 1320833 Tnfrsf14 tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator) gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15696194 1320833 Tnfrsf14 tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator) gene MP:0004752 decreased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:16237069 1320833 Tnfrsf14 tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator) gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17431181 1320833 Tnfrsf14 tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator) gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15696194 1320833 Tnfrsf14 tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator) gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:21347711 1320833 Tnfrsf14 tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator) gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21347711 1320833 Tnfrsf14 tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator) gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:21347711 1320833 Tnfrsf14 tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator) gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21347711 1320833 Tnfrsf14 tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator) gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21347711 1320833 Tnfrsf14 tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator) gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21347711 1320833 Tnfrsf14 tumor necrosis factor receptor superfamily, member 14 (herpesvirus entry mediator) gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:28114589 1320839 Kctd16 potassium channel tetramerisation domain containing 16 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20180118 MGI PMID:27717812 1320839 Kctd16 potassium channel tetramerisation domain containing 16 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20180118 MGI PMID:27717812 1320841 Dpm1 dolichyl-phosphate mannosyltransferase subunit 1, catalytic gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1320841 Dpm1 dolichyl-phosphate mannosyltransferase subunit 1, catalytic gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1320841 Dpm1 dolichyl-phosphate mannosyltransferase subunit 1, catalytic gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1320841 Dpm1 dolichyl-phosphate mannosyltransferase subunit 1, catalytic gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20190912 MGI PMID:29539633 1320841 Dpm1 dolichyl-phosphate mannosyltransferase subunit 1, catalytic gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1320841 Dpm1 dolichyl-phosphate mannosyltransferase subunit 1, catalytic gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1320841 Dpm1 dolichyl-phosphate mannosyltransferase subunit 1, catalytic gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320841 Dpm1 dolichyl-phosphate mannosyltransferase subunit 1, catalytic gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1320842 Tppp tubulin polymerization promoting protein gene MP:0000947 convulsive seizures IEA N RGD:5509061 20170105 MGI 1320842 Tppp tubulin polymerization promoting protein gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 1320842 Tppp tubulin polymerization promoting protein gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 1320842 Tppp tubulin polymerization promoting protein gene MP:0002608 increased hematocrit IEA N RGD:5509061 20160421 MGI 1320842 Tppp tubulin polymerization promoting protein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1320842 Tppp tubulin polymerization promoting protein gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20170105 MGI 1320842 Tppp tubulin polymerization promoting protein gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20160421 MGI 1320842 Tppp tubulin polymerization promoting protein gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201022 MGI 1320842 Tppp tubulin polymerization promoting protein gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160421 MGI 1320842 Tppp tubulin polymerization promoting protein gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20201022 MGI 1320842 Tppp tubulin polymerization promoting protein gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1320842 Tppp tubulin polymerization promoting protein gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20160421 MGI 1320842 Tppp tubulin polymerization promoting protein gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1320844 Pspc1 paraspeckle protein 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1320844 Pspc1 paraspeckle protein 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1320844 Pspc1 paraspeckle protein 1 gene MP:0000692 small spleen IEA N RGD:5509061 20210128 MGI 1320844 Pspc1 paraspeckle protein 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1320844 Pspc1 paraspeckle protein 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20201022 MGI 1320844 Pspc1 paraspeckle protein 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1320850 Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20190530 MGI PMID:27809299 1320850 Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20190530 MGI PMID:27809299 1320850 Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20190530 MGI PMID:30237863 1320850 Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20190530 MGI PMID:27809299 1320850 Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20190530 MGI PMID:30237863 1320850 Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2 gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20190530 MGI PMID:30237863 1320850 Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20190530 MGI PMID:30237863 1320850 Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190530 MGI PMID:30237863 1320850 Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20190530 MGI PMID:27809299 1320850 Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2 gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20190530 MGI PMID:27809299 1320850 Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20190530 MGI PMID:30237863 1320850 Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2 gene MP:0012075 impaired mammary gland growth during pregnancy IAGP N RGD:5509061 20190530 MGI PMID:27809299 1320850 Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2 gene MP:0012765 decreased alpha-beta T cell number IAGP N RGD:5509061 20190530 MGI PMID:30237863 1320850 Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2 gene MP:0013782 abnormal mammary duct terminal end bud morphology IAGP N RGD:5509061 20190530 MGI PMID:27809299 1320852 Tdrd3 tudor domain containing 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1320852 Tdrd3 tudor domain containing 3 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20150226 MGI PMID:24507716 1320852 Tdrd3 tudor domain containing 3 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20150226 MGI PMID:24507716 1320852 Tdrd3 tudor domain containing 3 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20150226 MGI PMID:24507716 1320852 Tdrd3 tudor domain containing 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1320854 Med10 mediator complex subunit 10 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1320854 Med10 mediator complex subunit 10 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1320854 Med10 mediator complex subunit 10 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 1320854 Med10 mediator complex subunit 10 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1320854 Med10 mediator complex subunit 10 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1320854 Med10 mediator complex subunit 10 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1320854 Med10 mediator complex subunit 10 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 1320854 Med10 mediator complex subunit 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320854 Med10 mediator complex subunit 10 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1320858 Rinl Ras and Rab interactor-like gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20240509 MGI PMID:37703004 1320858 Rinl Ras and Rab interactor-like gene MP:0005014 increased B cell number IAGP N RGD:5509061 20240509 MGI PMID:37703004 1320858 Rinl Ras and Rab interactor-like gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20240509 MGI PMID:37703004 1320858 Rinl Ras and Rab interactor-like gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20240509 MGI PMID:37703004 1320858 Rinl Ras and Rab interactor-like gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20240509 MGI PMID:37703004 1320858 Rinl Ras and Rab interactor-like gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1320858 Rinl Ras and Rab interactor-like gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20240509 MGI PMID:37703004 1320858 Rinl Ras and Rab interactor-like gene MP:0010188 abnormal T follicular helper cell differentiation IAGP N RGD:5509061 20240509 MGI PMID:37703004 1320858 Rinl Ras and Rab interactor-like gene MP:0020912 abnormal susceptibility to Riboviria infection IAGP N RGD:5509061 20240509 MGI PMID:37703004 1320860 Gtf2e2 general transcription factor II E, polypeptide 2 (beta subunit) gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20201022 MGI 1320860 Gtf2e2 general transcription factor II E, polypeptide 2 (beta subunit) gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1320860 Gtf2e2 general transcription factor II E, polypeptide 2 (beta subunit) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320860 Gtf2e2 general transcription factor II E, polypeptide 2 (beta subunit) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1320860 Gtf2e2 general transcription factor II E, polypeptide 2 (beta subunit) gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0004325 absent vestibular hair cells IAGP N RGD:5509061 20151001 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0004397 absent cochlear inner hair cells IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0004403 absent cochlear outer hair cells IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0011060 abnormal kinocilium morphology IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320862 Tmprss3 transmembrane protease, serine 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21454591 1320864 Nsun7 NOL1/NOP2/Sun domain family, member 7 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17442852 1320864 Nsun7 NOL1/NOP2/Sun domain family, member 7 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17442852 1320864 Nsun7 NOL1/NOP2/Sun domain family, member 7 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:17442852 1320864 Nsun7 NOL1/NOP2/Sun domain family, member 7 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220714 MGI PMID:16024820 1320864 Nsun7 NOL1/NOP2/Sun domain family, member 7 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20240523 MGI 1320864 Nsun7 NOL1/NOP2/Sun domain family, member 7 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:17442852 1320864 Nsun7 NOL1/NOP2/Sun domain family, member 7 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:17442852 1320866 Tut4 terminal uridylyl transferase 4 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200402 MGI 1320866 Tut4 terminal uridylyl transferase 4 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20181227 MGI PMID:28792939 1320866 Tut4 terminal uridylyl transferase 4 gene MP:0001258 decreased body length IEA N RGD:5509061 20181227 MGI 1320866 Tut4 terminal uridylyl transferase 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23209448 1320866 Tut4 terminal uridylyl transferase 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23209448 1320866 Tut4 terminal uridylyl transferase 4 gene MP:0001926 female infertility IAGP N RGD:5509061 20181227 MGI PMID:28792939 1320866 Tut4 terminal uridylyl transferase 4 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:23209448 1320866 Tut4 terminal uridylyl transferase 4 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23209448 1320866 Tut4 terminal uridylyl transferase 4 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20201022 MGI 1320866 Tut4 terminal uridylyl transferase 4 gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20181227 MGI PMID:28792939 1320866 Tut4 terminal uridylyl transferase 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23209448 1320866 Tut4 terminal uridylyl transferase 4 gene MP:0014445 abnormal spindle assembly in female meiosis IAGP N RGD:5509061 20240509 MGI PMID:28792939 1320870 T brachyury, T-box transcription factor T gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11071760 1320870 T brachyury, T-box transcription factor T gene MP:0000138 absent vertebrae IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:10349618 1320870 T brachyury, T-box transcription factor T gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10349618 1320870 T brachyury, T-box transcription factor T gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:10723731 1320870 T brachyury, T-box transcription factor T gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0000461 decreased presacral vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:13575656 1320870 T brachyury, T-box transcription factor T gene MP:0000461 decreased presacral vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:10723731 1320870 T brachyury, T-box transcription factor T gene MP:0000589 thin tail IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:10835400 1320870 T brachyury, T-box transcription factor T gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:11071760 1320870 T brachyury, T-box transcription factor T gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:13575656 1320870 T brachyury, T-box transcription factor T gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:15384171 1320870 T brachyury, T-box transcription factor T gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:20809182 1320870 T brachyury, T-box transcription factor T gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:23359409 1320870 T brachyury, T-box transcription factor T gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:8436292 1320870 T brachyury, T-box transcription factor T gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:9383288 1320870 T brachyury, T-box transcription factor T gene MP:0000592 short tail IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0000923 abnormal roof plate morphology IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:15384171 1320870 T brachyury, T-box transcription factor T gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:12533796 1320870 T brachyury, T-box transcription factor T gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:15384171 1320870 T brachyury, T-box transcription factor T gene MP:0000932 absent notochord IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0001216 abnormal epidermal layer morphology IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10723731 1320870 T brachyury, T-box transcription factor T gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12533796 1320870 T brachyury, T-box transcription factor T gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:11071760 1320870 T brachyury, T-box transcription factor T gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:13575656 1320870 T brachyury, T-box transcription factor T gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0001684 abnormal axial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12140191 1320870 T brachyury, T-box transcription factor T gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:10723731 1320870 T brachyury, T-box transcription factor T gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:15384171 1320870 T brachyury, T-box transcription factor T gene MP:0001698 decreased embryo size IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10723731 1320870 T brachyury, T-box transcription factor T gene MP:0001712 abnormal placenta development IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:1218735 1320870 T brachyury, T-box transcription factor T gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12533796 1320870 T brachyury, T-box transcription factor T gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:10835400 1320870 T brachyury, T-box transcription factor T gene MP:0001914 hemorrhage IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10835400 1320870 T brachyury, T-box transcription factor T gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10835400 1320870 T brachyury, T-box transcription factor T gene MP:0001935 decreased litter size IEA N RGD:5509061 20141003 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0002080 prenatal lethality IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:1003081 1320870 T brachyury, T-box transcription factor T gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:10932191 1320870 T brachyury, T-box transcription factor T gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:23359409 1320870 T brachyury, T-box transcription factor T gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:8436292 1320870 T brachyury, T-box transcription factor T gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20150702 MGI PMID:17247438 1320870 T brachyury, T-box transcription factor T gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10617567 1320870 T brachyury, T-box transcription factor T gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10723731 1320870 T brachyury, T-box transcription factor T gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:924142 1320870 T brachyury, T-box transcription factor T gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:12140191 1320870 T brachyury, T-box transcription factor T gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0002632 vestigial tail IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:10723731 1320870 T brachyury, T-box transcription factor T gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:12140191 1320870 T brachyury, T-box transcription factor T gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:13575656 1320870 T brachyury, T-box transcription factor T gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0002861 abnormal tail bud morphology IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0002861 abnormal tail bud morphology IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0003047 abnormal thoracic vertebrae morphology IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11071760 1320870 T brachyury, T-box transcription factor T gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:20809182 1320870 T brachyury, T-box transcription factor T gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:23359409 1320870 T brachyury, T-box transcription factor T gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:12140191 1320870 T brachyury, T-box transcription factor T gene MP:0003345 decreased rib number IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:10617567 1320870 T brachyury, T-box transcription factor T gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:1003081 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:15384171 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:1859671 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:2016041 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:2318411 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:23359409 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:3422415 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:3653686 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:6722884 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:7461454 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:8690273 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:924142 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20150702 MGI PMID:17247438 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20150702 MGI PMID:3678828 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20170817 MGI PMID:17247632 1320870 T brachyury, T-box transcription factor T gene MP:0003456 absent tail IAGP N RGD:5509061 20230601 MGI PMID:28565025 1320870 T brachyury, T-box transcription factor T gene MP:0003861 abnormal nervous system development IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0003885 abnormal rostral-caudal body axis extension IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10723731 1320870 T brachyury, T-box transcription factor T gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:10835400 1320870 T brachyury, T-box transcription factor T gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:7207588 1320870 T brachyury, T-box transcription factor T gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:7461454 1320870 T brachyury, T-box transcription factor T gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20150702 MGI PMID:17247438 1320870 T brachyury, T-box transcription factor T gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20150702 MGI PMID:3678828 1320870 T brachyury, T-box transcription factor T gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20230601 MGI PMID:28565025 1320870 T brachyury, T-box transcription factor T gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12533796 1320870 T brachyury, T-box transcription factor T gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:10723731 1320870 T brachyury, T-box transcription factor T gene MP:0004387 abnormal prechordal plate morphology IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20141003 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0004603 absent vertebral arch IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0004653 absent caudal vertebrae IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0004656 absent sacral vertebrae IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0004659 abnormal odontoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0004668 absent vertebral body IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0004712 notochord degeneration IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0004713 split notochord IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0004787 abnormal dorsal aorta morphology IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:10835400 1320870 T brachyury, T-box transcription factor T gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0005226 abnormal vertebral arch development IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0005227 abnormal vertebral body development IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0005244 hemopericardium IEA N RGD:5509061 20141003 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0006281 abnormal tail development IEA N RGD:5509061 20141003 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0006386 absent somites IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0006392 abnormal nucleus pulposus morphology IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:3422415 1320870 T brachyury, T-box transcription factor T gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:1859671 1320870 T brachyury, T-box transcription factor T gene MP:0008854 bleb IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0008999 absent anus IEA N RGD:5509061 20141003 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0009331 absent primitive node IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0009929 meningomyelocele IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10835400 1320870 T brachyury, T-box transcription factor T gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10835400 1320870 T brachyury, T-box transcription factor T gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1859671 1320870 T brachyury, T-box transcription factor T gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15384171 1320870 T brachyury, T-box transcription factor T gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23359409 1320870 T brachyury, T-box transcription factor T gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9383288 1320870 T brachyury, T-box transcription factor T gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12140191 1320870 T brachyury, T-box transcription factor T gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10723731 1320870 T brachyury, T-box transcription factor T gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1218735 1320870 T brachyury, T-box transcription factor T gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12533796 1320870 T brachyury, T-box transcription factor T gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20809182 1320870 T brachyury, T-box transcription factor T gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0011495 abnormal head shape IEA N RGD:5509061 20111208 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0012063 absent tail bud IAGP N RGD:5509061 20141003 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0012063 absent tail bud IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0012082 delayed heart development IEA N RGD:5509061 20141003 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0012259 meningocele IAGP N RGD:5509061 20200910 MGI PMID:2658196 1320870 T brachyury, T-box transcription factor T gene MP:0012501 abnormal pericardial cavity morphology IEA N RGD:5509061 20141003 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0012707 incomplete caudal neuropore closure IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0012714 decreased ventral ectodermal ridge size IAGP N RGD:5509061 20141003 MGI PMID:13575656 1320870 T brachyury, T-box transcription factor T gene MP:0012740 abnormal posterior primitive streak morphology IAGP N RGD:5509061 20190228 MGI PMID:8293872 1320870 T brachyury, T-box transcription factor T gene MP:0013164 abnormal forelimb bud morphology IEA N RGD:5509061 20141003 MGI 1320870 T brachyury, T-box transcription factor T gene MP:0013165 absent forelimb buds IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320870 T brachyury, T-box transcription factor T gene MP:0013168 absent hindlimb buds IAGP N RGD:5509061 20141003 MGI PMID:5906493 1320876 Tbx19 T-box 19 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20171102 MGI PMID:12651892 1320876 Tbx19 T-box 19 gene MP:0000640 adrenal gland hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:12651892 1320876 Tbx19 T-box 19 gene MP:0000676 abnormal body water content IAGP N RGD:5509061 20171102 MGI PMID:12651892 1320876 Tbx19 T-box 19 gene MP:0002664 decreased circulating adrenocorticotropin level IAGP N RGD:5509061 20171102 MGI PMID:12651892 1320876 Tbx19 T-box 19 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20171102 MGI PMID:12651892 1320876 Tbx19 T-box 19 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20171102 MGI PMID:12651892 1320876 Tbx19 T-box 19 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20171102 MGI PMID:12651892 1320876 Tbx19 T-box 19 gene MP:0008237 abnormal ventral coat pigmentation IAGP N RGD:5509061 20171102 MGI PMID:12651892 1320876 Tbx19 T-box 19 gene MP:0008341 decreased corticotroph cell number IAGP N RGD:5509061 20171102 MGI PMID:12651892 1320878 Kif16b kinesin family member 16B gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1320878 Kif16b kinesin family member 16B gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1320878 Kif16b kinesin family member 16B gene MP:0000495 abnormal colon morphology IEA N RGD:5509061 20230119 MGI 1320878 Kif16b kinesin family member 16B gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1320878 Kif16b kinesin family member 16B gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1320878 Kif16b kinesin family member 16B gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1320878 Kif16b kinesin family member 16B gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1320878 Kif16b kinesin family member 16B gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230119 MGI 1320878 Kif16b kinesin family member 16B gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20230119 MGI 1320878 Kif16b kinesin family member 16B gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:21238925 1320878 Kif16b kinesin family member 16B gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:21238925 1320878 Kif16b kinesin family member 16B gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230119 MGI 1320878 Kif16b kinesin family member 16B gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1320878 Kif16b kinesin family member 16B gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1320878 Kif16b kinesin family member 16B gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 1320878 Kif16b kinesin family member 16B gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20230119 MGI 1320878 Kif16b kinesin family member 16B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21238925 1320878 Kif16b kinesin family member 16B gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:21238925 1320878 Kif16b kinesin family member 16B gene MP:0011184 absent embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:21238925 1320879 Tbc1d9b TBC1 domain family, member 9B gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220811 MGI 1320879 Tbc1d9b TBC1 domain family, member 9B gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1320879 Tbc1d9b TBC1 domain family, member 9B gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1320879 Tbc1d9b TBC1 domain family, member 9B gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1320879 Tbc1d9b TBC1 domain family, member 9B gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0003981 decreased circulating phospholipid level IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0010331 abnormal apolipoprotein level IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0010332 abnormal circulating apolipoprotein level IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0020151 abnormal circulating non-HDL cholesterol level IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320880 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains gene MP:0020868 decreased lipogenesis IAGP N RGD:5509061 20210311 MGI PMID:32912065 1320888 Tfr2 transferrin receptor 2 gene MP:0000226 abnormal mean corpuscular volume IEA N RGD:5509061 20201022 MGI 1320888 Tfr2 transferrin receptor 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1320888 Tfr2 transferrin receptor 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1320888 Tfr2 transferrin receptor 2 gene MP:0000492 abnormal rectum morphology IEA N RGD:5509061 20210520 MGI 1320888 Tfr2 transferrin receptor 2 gene MP:0000495 abnormal colon morphology IEA N RGD:5509061 20210520 MGI 1320888 Tfr2 transferrin receptor 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1320888 Tfr2 transferrin receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20179178 1320888 Tfr2 transferrin receptor 2 gene MP:0001586 abnormal erythrocyte cell number IEA N RGD:5509061 20201022 MGI 1320888 Tfr2 transferrin receptor 2 gene MP:0001589 abnormal mean corpuscular hemoglobin IEA N RGD:5509061 20201022 MGI 1320888 Tfr2 transferrin receptor 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 1320888 Tfr2 transferrin receptor 2 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:20179178 1320888 Tfr2 transferrin receptor 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20201022 MGI 1320888 Tfr2 transferrin receptor 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20201022 MGI 1320888 Tfr2 transferrin receptor 2 gene MP:0005563 abnormal hemoglobin content IEA N RGD:5509061 20211021 MGI 1320888 Tfr2 transferrin receptor 2 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20179178 1320888 Tfr2 transferrin receptor 2 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12134060 1320888 Tfr2 transferrin receptor 2 gene MP:0005638 hemochromatosis IAGP N RGD:5509061 20141003 MGI PMID:15951546 1320888 Tfr2 transferrin receptor 2 gene MP:0005640 abnormal mean corpuscular hemoglobin concentration IEA N RGD:5509061 20201022 MGI 1320888 Tfr2 transferrin receptor 2 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 1320888 Tfr2 transferrin receptor 2 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:12134060 1320888 Tfr2 transferrin receptor 2 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:15951546 1320888 Tfr2 transferrin receptor 2 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:20179178 1320888 Tfr2 transferrin receptor 2 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:12134060 1320888 Tfr2 transferrin receptor 2 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:15951546 1320888 Tfr2 transferrin receptor 2 gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:20179178 1320888 Tfr2 transferrin receptor 2 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:12134060 1320888 Tfr2 transferrin receptor 2 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:15951546 1320888 Tfr2 transferrin receptor 2 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:20179178 1320888 Tfr2 transferrin receptor 2 gene MP:0008955 increased cellular hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20179178 1320888 Tfr2 transferrin receptor 2 gene MP:0011890 increased circulating ferritin level IEA N RGD:5509061 20141003 MGI 1320891 Ndc80 NDC80 kinetochore complex component gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240919 MGI 1320891 Ndc80 NDC80 kinetochore complex component gene MP:0004024 aneuploidy IAGP N RGD:5509061 20200917 MGI PMID:32461611 1320891 Ndc80 NDC80 kinetochore complex component gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20200917 MGI PMID:32461611 1320891 Ndc80 NDC80 kinetochore complex component gene MP:0009769 abnormal meiotic spindle assembly checkpoint IAGP N RGD:5509061 20200917 MGI PMID:32461611 1320891 Ndc80 NDC80 kinetochore complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1320891 Ndc80 NDC80 kinetochore complex component gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1320891 Ndc80 NDC80 kinetochore complex component gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240919 MGI 1320893 Jchain immunoglobulin joining chain gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:11535625 1320893 Jchain immunoglobulin joining chain gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11535625 1320893 Jchain immunoglobulin joining chain gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:9710213 1320893 Jchain immunoglobulin joining chain gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10395687 1320893 Jchain immunoglobulin joining chain gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11535625 1320893 Jchain immunoglobulin joining chain gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9710213 1320893 Jchain immunoglobulin joining chain gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9710213 1320893 Jchain immunoglobulin joining chain gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10395687 1320893 Jchain immunoglobulin joining chain gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10395687 1320893 Jchain immunoglobulin joining chain gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7500036 1320893 Jchain immunoglobulin joining chain gene MP:0002473 impaired complement classical pathway IAGP N RGD:5509061 20141003 MGI PMID:9710213 1320893 Jchain immunoglobulin joining chain gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:10395687 1320893 Jchain immunoglobulin joining chain gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11535625 1320893 Jchain immunoglobulin joining chain gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15175647 1320893 Jchain immunoglobulin joining chain gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:7500036 1320893 Jchain immunoglobulin joining chain gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:8752925 1320893 Jchain immunoglobulin joining chain gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:9710213 1320893 Jchain immunoglobulin joining chain gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:8752925 1320893 Jchain immunoglobulin joining chain gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:7500036 1320893 Jchain immunoglobulin joining chain gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17056558 1320893 Jchain immunoglobulin joining chain gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:10395687 1320893 Jchain immunoglobulin joining chain gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:9710213 1320893 Jchain immunoglobulin joining chain gene MP:0008864 abnormal intestinal secretion IAGP N RGD:5509061 20141003 MGI PMID:7500036 1320893 Jchain immunoglobulin joining chain gene MP:0008864 abnormal intestinal secretion IAGP N RGD:5509061 20141003 MGI PMID:8752925 1320893 Jchain immunoglobulin joining chain gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:10814580 1320893 Jchain immunoglobulin joining chain gene MP:0031025 decreased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:10814580 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9529147 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20150219 MGI PMID:24557836 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20150219 MGI PMID:24557836 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:9529147 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:9529147 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20240125 MGI PMID:35064213 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20240125 MGI PMID:35064213 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9529147 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9529147 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22327219 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240125 MGI PMID:35064213 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:9529147 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20150219 MGI PMID:24557836 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:9529147 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:9529147 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9529147 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0003717 pallor IAGP N RGD:5509061 20150219 MGI PMID:24557836 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0003865 lymph node inflammation IAGP N RGD:5509061 20200618 MGI PMID:9529147 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0005535 abnormal body temperature IAGP N RGD:5509061 20150219 MGI PMID:24557836 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:9529147 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20150219 MGI PMID:24557836 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150219 MGI PMID:24557836 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20150219 MGI PMID:24557836 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20150219 MGI PMID:24557836 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9529147 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20240125 MGI PMID:35064213 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20150219 MGI PMID:24557836 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20150219 MGI PMID:24557836 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0012556 increased cell death IAGP N RGD:5509061 20150219 MGI PMID:24557836 1320897 Ripk1 receptor (TNFRSF)-interacting serine-threonine kinase 1 gene MP:0031052 lymph node necrosis IAGP N RGD:5509061 20200618 MGI PMID:9529147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15136147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15136147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15136147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15136147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:15136147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0000935 abnormal folding of telencephalic vesicles IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15136147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15136147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:15136147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:15136147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15136147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15136147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0004081 abnormal globus pallidus morphology IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0004592 small mandible IAGP N RGD:5509061 20171102 MGI PMID:15136147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0004870 small premaxilla IAGP N RGD:5509061 20171102 MGI PMID:15136147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:15136147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15136147 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15736266 1320900 Zic5 zinc finger protein of the cerebellum 5 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:15736266 1320903 Liph lipase, member H gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:21857648 1320903 Liph lipase, member H gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:21857648 1320903 Liph lipase, member H gene MP:0001279 wavy vibrissae IAGP N RGD:5509061 20141003 MGI PMID:21857648 1320903 Liph lipase, member H gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20141003 MGI PMID:21857648 1320903 Liph lipase, member H gene MP:0003812 abnormal hair medulla IAGP N RGD:5509061 20141003 MGI PMID:21857648 1320903 Liph lipase, member H gene MP:0003846 matted coat IAGP N RGD:5509061 20141003 MGI PMID:21857648 1320903 Liph lipase, member H gene MP:0008731 abnormal hair shaft melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:21857648 1320903 Liph lipase, member H gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:21857648 1320905 Srrm2 serine/arginine repetitive matrix 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320907 Ddb2 damage specific DNA binding protein 2 gene MP:0001203 increased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:14769931 1320907 Ddb2 damage specific DNA binding protein 2 gene MP:0001203 increased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:16288018 1320907 Ddb2 damage specific DNA binding protein 2 gene MP:0001203 increased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:17127714 1320907 Ddb2 damage specific DNA binding protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14769931 1320907 Ddb2 damage specific DNA binding protein 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15558025 1320907 Ddb2 damage specific DNA binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15558025 1320907 Ddb2 damage specific DNA binding protein 2 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16288018 1320907 Ddb2 damage specific DNA binding protein 2 gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:14769931 1320907 Ddb2 damage specific DNA binding protein 2 gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:14769931 1320912 Eea1 early endosome antigen 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1320912 Eea1 early endosome antigen 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20210128 MGI 1320912 Eea1 early endosome antigen 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1320913 Fermt3 fermitin family member 3 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:18278053 1320913 Fermt3 fermitin family member 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20160519 MGI PMID:24969775 1320913 Fermt3 fermitin family member 3 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18278053 1320913 Fermt3 fermitin family member 3 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:23980064 1320913 Fermt3 fermitin family member 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18662549 1320913 Fermt3 fermitin family member 3 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18278053 1320913 Fermt3 fermitin family member 3 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1320913 Fermt3 fermitin family member 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18662549 1320913 Fermt3 fermitin family member 3 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18278053 1320913 Fermt3 fermitin family member 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23980064 1320913 Fermt3 fermitin family member 3 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:23980064 1320913 Fermt3 fermitin family member 3 gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23980064 1320913 Fermt3 fermitin family member 3 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23980064 1320913 Fermt3 fermitin family member 3 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18662549 1320913 Fermt3 fermitin family member 3 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:18662549 1320913 Fermt3 fermitin family member 3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18662549 1320913 Fermt3 fermitin family member 3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20160519 MGI PMID:24969775 1320913 Fermt3 fermitin family member 3 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:18662549 1320913 Fermt3 fermitin family member 3 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:18278053 1320913 Fermt3 fermitin family member 3 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20160519 MGI PMID:24969775 1320913 Fermt3 fermitin family member 3 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:18278053 1320913 Fermt3 fermitin family member 3 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20160519 MGI PMID:24969775 1320913 Fermt3 fermitin family member 3 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:18278053 1320913 Fermt3 fermitin family member 3 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20160519 MGI PMID:24969775 1320913 Fermt3 fermitin family member 3 gene MP:0008816 petechiae IAGP N RGD:5509061 20141003 MGI PMID:18278053 1320913 Fermt3 fermitin family member 3 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18662549 1320913 Fermt3 fermitin family member 3 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:18278053 1320913 Fermt3 fermitin family member 3 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20160519 MGI PMID:24969775 1320913 Fermt3 fermitin family member 3 gene MP:0010177 acanthocytosis IAGP N RGD:5509061 20160519 MGI PMID:24969775 1320913 Fermt3 fermitin family member 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18278053 1320913 Fermt3 fermitin family member 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320913 Fermt3 fermitin family member 3 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:24969775 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23360989 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:23469192 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:23360989 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:23360989 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:23469192 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:23360989 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:23360989 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23360989 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:23469192 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0006323 abnormal extraembryonic mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:23469192 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0008391 abnormal primordial germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23469192 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:23469192 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23469192 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23469192 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0011187 abnormal parietal endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:23469192 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0011200 abnormal extraembryonic coelom morphology IAGP N RGD:5509061 20141003 MGI PMID:23469192 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0011257 abnormal head fold morphology IAGP N RGD:5509061 20141003 MGI PMID:23469192 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20141003 MGI PMID:23360989 1320918 Ctdnep1 CTD nuclear envelope phosphatase 1 gene MP:0011371 decreased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23360989 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0001260 increased body weight IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0001261 obese IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0001399 hyperactivity IEA N RGD:5509061 20190502 MGI 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0001433 polyphagia IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0011939 increased food intake IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320924 Gpr61 G protein-coupled receptor 61 gene MP:0020867 increased lipogenesis IAGP N RGD:5509061 20210318 MGI PMID:21971119 1320931 Ulk2 unc-51 like kinase 2 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20111116 MGI 1320931 Ulk2 unc-51 like kinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21690395 1320931 Ulk2 unc-51 like kinase 2 gene MP:0010166 increased response to stress-induced hyperthermia IEA N RGD:5509061 20111116 MGI 1320931 Ulk2 unc-51 like kinase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21690395 1320932 Arsk arylsulfatase K gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20210415 MGI PMID:32856704 1320932 Arsk arylsulfatase K gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1320932 Arsk arylsulfatase K gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20210415 MGI PMID:32856704 1320932 Arsk arylsulfatase K gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20210415 MGI PMID:32856704 1320932 Arsk arylsulfatase K gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20210415 MGI PMID:32856704 1320932 Arsk arylsulfatase K gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20210415 MGI PMID:32856704 1320932 Arsk arylsulfatase K gene MP:0011333 abnormal kidney inner medulla morphology IAGP N RGD:5509061 20210415 MGI PMID:32856704 1320932 Arsk arylsulfatase K gene MP:0011378 abnormal kidney outer medulla inner stripe morphology IAGP N RGD:5509061 20210415 MGI PMID:32856704 1320932 Arsk arylsulfatase K gene MP:0011475 abnormal glycosaminoglycan level IAGP N RGD:5509061 20210415 MGI PMID:32856704 1320940 Muc19 mucin 19 gene MP:0004035 abnormal sublingual gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12847143 1320940 Muc19 mucin 19 gene MP:0004035 abnormal sublingual gland morphology IAGP N RGD:5509061 20141003 MGI PMID:23580649 1320940 Muc19 mucin 19 gene MP:0004035 abnormal sublingual gland morphology IAGP N RGD:5509061 20141003 MGI PMID:3400771 1320940 Muc19 mucin 19 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:8077681 1320940 Muc19 mucin 19 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20150618 MGI PMID:25447050 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:23813972 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23813972 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0001785 edema IAGP N RGD:5509061 20150528 MGI PMID:23942972 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20150528 MGI PMID:23942972 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20150528 MGI PMID:23942972 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0003878 abnormal ear physiology IAGP N RGD:5509061 20141003 MGI PMID:19586905 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0004292 abnormal spiral ligament fibrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0004427 abnormal vestibular labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:19586905 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:19586905 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0004814 reduced linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:19586905 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23813972 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20150528 MGI PMID:23942972 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0005544 cornea deposits IAGP N RGD:5509061 20141003 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20150528 MGI PMID:23942972 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19586905 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20150528 MGI PMID:23942972 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20150528 MGI PMID:23942972 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0009742 increased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0011435 increased urine magnesium level IAGP N RGD:5509061 20141003 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0011436 decreased urine magnesium level IAGP N RGD:5509061 20150528 MGI PMID:23942972 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0011460 decreased urine chloride ion level IAGP N RGD:5509061 20180927 MGI PMID:23942972 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:23813972 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20150528 MGI PMID:23942972 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0020854 increased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0030633 decreased urine creatine level IAGP N RGD:5509061 20180927 MGI PMID:23942972 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0031178 increased Descemet membrane thickness IAGP N RGD:5509061 20201119 MGI PMID:20185830 1320942 Slc4a11 solute carrier family 4, sodium bicarbonate transporter-like, member 11 gene MP:0031178 increased Descemet membrane thickness IAGP N RGD:5509061 20201119 MGI PMID:23942972 1320944 Dapp1 dual adaptor for phosphotyrosine and 3-phosphoinositides 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:14588241 1320944 Dapp1 dual adaptor for phosphotyrosine and 3-phosphoinositides 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:14563325 1320944 Dapp1 dual adaptor for phosphotyrosine and 3-phosphoinositides 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:14588241 1320944 Dapp1 dual adaptor for phosphotyrosine and 3-phosphoinositides 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14563325 1320944 Dapp1 dual adaptor for phosphotyrosine and 3-phosphoinositides 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14588241 1320944 Dapp1 dual adaptor for phosphotyrosine and 3-phosphoinositides 1 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:14563325 1320944 Dapp1 dual adaptor for phosphotyrosine and 3-phosphoinositides 1 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:14563325 1320944 Dapp1 dual adaptor for phosphotyrosine and 3-phosphoinositides 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:14563325 1320944 Dapp1 dual adaptor for phosphotyrosine and 3-phosphoinositides 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:14588241 1320946 Snx5 sorting nexin 5 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 1320946 Snx5 sorting nexin 5 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1320946 Snx5 sorting nexin 5 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1320946 Snx5 sorting nexin 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23526992 1320946 Snx5 sorting nexin 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23526992 1320946 Snx5 sorting nexin 5 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:23526992 1320946 Snx5 sorting nexin 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23526992 1320946 Snx5 sorting nexin 5 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:23526992 1320946 Snx5 sorting nexin 5 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:23526992 1320946 Snx5 sorting nexin 5 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:23526992 1320946 Snx5 sorting nexin 5 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20160804 MGI 1320946 Snx5 sorting nexin 5 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1320946 Snx5 sorting nexin 5 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1320946 Snx5 sorting nexin 5 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20160804 MGI 1320946 Snx5 sorting nexin 5 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:23526992 1320946 Snx5 sorting nexin 5 gene MP:0010816 decreased type I pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:23526992 1320946 Snx5 sorting nexin 5 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:23526992 1320946 Snx5 sorting nexin 5 gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20141003 MGI PMID:23526992 1320946 Snx5 sorting nexin 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23526992 1320946 Snx5 sorting nexin 5 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23526992 1320946 Snx5 sorting nexin 5 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23526992 1320951 Snrpb2 U2 small nuclear ribonucleoprotein B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1320954 Washc1 WASH complex subunit 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:23974797 1320954 Washc1 WASH complex subunit 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:23974797 1320954 Washc1 WASH complex subunit 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22718907 1320954 Washc1 WASH complex subunit 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23974797 1320954 Washc1 WASH complex subunit 1 gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:23974797 1320954 Washc1 WASH complex subunit 1 gene MP:0011200 abnormal extraembryonic coelom morphology IAGP N RGD:5509061 20141003 MGI PMID:23974797 1320954 Washc1 WASH complex subunit 1 gene MP:0011202 abnormal ectoplacental cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:23974797 1320954 Washc1 WASH complex subunit 1 gene MP:0012556 increased cell death IAGP N RGD:5509061 20141003 MGI PMID:23974797 1320956 Slc26a6 solute carrier family 26, member 6 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:15574486 1320956 Slc26a6 solute carrier family 26, member 6 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17170027 1320956 Slc26a6 solute carrier family 26, member 6 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:15574486 1320956 Slc26a6 solute carrier family 26, member 6 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:17053783 1320956 Slc26a6 solute carrier family 26, member 6 gene MP:0002694 abnormal pancreas secretion IAGP N RGD:5509061 20141003 MGI PMID:17053783 1320956 Slc26a6 solute carrier family 26, member 6 gene MP:0005360 urolithiasis IAGP N RGD:5509061 20141003 MGI PMID:16532010 1320956 Slc26a6 solute carrier family 26, member 6 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16532010 1320956 Slc26a6 solute carrier family 26, member 6 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16532010 1320958 Polr2j polymerase (RNA) II (DNA directed) polypeptide J gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20241017 MGI 1320958 Polr2j polymerase (RNA) II (DNA directed) polypeptide J gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241017 MGI 1320958 Polr2j polymerase (RNA) II (DNA directed) polypeptide J gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241017 MGI 1320958 Polr2j polymerase (RNA) II (DNA directed) polypeptide J gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1320958 Polr2j polymerase (RNA) II (DNA directed) polypeptide J gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20241017 MGI 1320960 Ino80c INO80 complex subunit C gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1320960 Ino80c INO80 complex subunit C gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20210826 MGI 1320960 Ino80c INO80 complex subunit C gene MP:0001293 anophthalmia IEA N RGD:5509061 20210826 MGI 1320960 Ino80c INO80 complex subunit C gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210826 MGI 1320960 Ino80c INO80 complex subunit C gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20210826 MGI 1320960 Ino80c INO80 complex subunit C gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210826 MGI 1320960 Ino80c INO80 complex subunit C gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1320960 Ino80c INO80 complex subunit C gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20240523 MGI 1320960 Ino80c INO80 complex subunit C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1320960 Ino80c INO80 complex subunit C gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20210826 MGI 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20151126 MGI PMID:25673119 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20151126 MGI PMID:25673119 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20220929 MGI PMID:35127681 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9374397 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:15728667 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000155 asymmetric rib joints IAGP N RGD:5509061 20141003 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:23979902 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000414 alopecia IAGP N RGD:5509061 20151126 MGI PMID:25673119 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000422 delayed hair appearance IEA N RGD:5509061 20111116 MGI 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000445 short snout IAGP N RGD:5509061 20151126 MGI PMID:25673119 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000449 broad nasal bridge IAGP N RGD:5509061 20220929 MGI PMID:35127681 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9268572 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9374397 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9636085 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000562 polydactyly IAGP N RGD:5509061 20151126 MGI PMID:25673119 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:23979902 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:9374397 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:23979902 1320964 Alx4 aristaless-like homeobox 4 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20151126 MGI PMID:25673119 1320964 Alx4 aristaless-like homeobox 4 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:23979902 1320964 Alx4 aristaless-like homeobox 4 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20151126 MGI PMID:25673119 1320964 Alx4 aristaless-like homeobox 4 gene MP:0001304 cataract IAGP N RGD:5509061 20151126 MGI PMID:25673119 1320964 Alx4 aristaless-like homeobox 4 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23979902 1320964 Alx4 aristaless-like homeobox 4 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:9636085 1320964 Alx4 aristaless-like homeobox 4 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9374397 1320964 Alx4 aristaless-like homeobox 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:23979902 1320964 Alx4 aristaless-like homeobox 4 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20171102 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20220929 MGI PMID:35127681 1320964 Alx4 aristaless-like homeobox 4 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:23979902 1320964 Alx4 aristaless-like homeobox 4 gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20141003 MGI PMID:23979902 1320964 Alx4 aristaless-like homeobox 4 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004339 absent clavicle IAGP N RGD:5509061 20141003 MGI PMID:15728667 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004343 small scapula IAGP N RGD:5509061 20141003 MGI PMID:15728667 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004347 abnormal scapular spine morphology IAGP N RGD:5509061 20141003 MGI PMID:15728667 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20171102 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20141003 MGI PMID:23979902 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20171102 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004422 small temporal bone IAGP N RGD:5509061 20171102 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004441 small occipital bone IAGP N RGD:5509061 20171102 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20220929 MGI PMID:35127681 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004459 small alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004592 small mandible IAGP N RGD:5509061 20171102 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004691 absent pubis IAGP N RGD:5509061 20141003 MGI PMID:23979902 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004692 small pubis IAGP N RGD:5509061 20141003 MGI PMID:15728667 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20171123 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15728667 1320964 Alx4 aristaless-like homeobox 4 gene MP:0006411 upturned snout IEA N RGD:5509061 20111116 MGI 1320964 Alx4 aristaless-like homeobox 4 gene MP:0008430 short temporal bone squamous part IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20220929 MGI PMID:35127681 1320964 Alx4 aristaless-like homeobox 4 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:23979902 1320964 Alx4 aristaless-like homeobox 4 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9636085 1320964 Alx4 aristaless-like homeobox 4 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20151126 MGI PMID:25673119 1320964 Alx4 aristaless-like homeobox 4 gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20220929 MGI PMID:35127681 1320964 Alx4 aristaless-like homeobox 4 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20220929 MGI PMID:35127681 1320964 Alx4 aristaless-like homeobox 4 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0010202 focal dorsal hair loss IEA N RGD:5509061 20111116 MGI 1320964 Alx4 aristaless-like homeobox 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23979902 1320964 Alx4 aristaless-like homeobox 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9374397 1320964 Alx4 aristaless-like homeobox 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20151126 MGI PMID:25673119 1320964 Alx4 aristaless-like homeobox 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9636085 1320964 Alx4 aristaless-like homeobox 4 gene MP:0012528 abnormal zone of polarizing activity morphology IAGP N RGD:5509061 20141003 MGI PMID:9374397 1320964 Alx4 aristaless-like homeobox 4 gene MP:0030034 depressed nasal bridge IAGP N RGD:5509061 20220929 MGI PMID:35127681 1320964 Alx4 aristaless-like homeobox 4 gene MP:0030116 bifid nasal tip IAGP N RGD:5509061 20170928 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0030117 bifid nose IAGP N RGD:5509061 20170928 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0030193 short philtrum IAGP N RGD:5509061 20220929 MGI PMID:35127681 1320964 Alx4 aristaless-like homeobox 4 gene MP:0030200 abnormal nasal septum cartilage morphology IAGP N RGD:5509061 20171012 MGI PMID:9847249 1320964 Alx4 aristaless-like homeobox 4 gene MP:0030301 abnormal maxillary frontal process morphology IAGP N RGD:5509061 20171102 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0030384 short facial bone IAGP N RGD:5509061 20171207 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0030385 absent facial bone IAGP N RGD:5509061 20171207 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0030388 large fontanelles IAGP N RGD:5509061 20171207 MGI PMID:11641221 1320964 Alx4 aristaless-like homeobox 4 gene MP:0030833 small acromion IAGP N RGD:5509061 20181018 MGI PMID:15728667 1320964 Alx4 aristaless-like homeobox 4 gene MP:0031445 midline cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:35127681 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:3711636 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:12847290 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0000371 diluted coat color IAGP N RGD:5509061 20230601 MGI PMID:17807638 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:3711636 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:10193444 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:8441253 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:3711636 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:8441253 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:5559839 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:3711636 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:3711636 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:15109702 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:5559839 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:5559839 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:3711636 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:12485443 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001760 abnormal urine enzyme level IAGP N RGD:5509061 20141003 MGI PMID:115747 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:8441253 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20141003 MGI PMID:8441253 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:8441253 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10193444 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:3711636 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:8441253 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:115747 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12009785 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:8441253 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:8441253 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20141003 MGI PMID:12009785 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:5559839 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20141003 MGI PMID:15109702 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20141003 MGI PMID:5559839 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20210520 MGI 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:3711636 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:7089489 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:3711636 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:133823 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:8441253 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12485443 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:3711636 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:6696991 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0004812 abnormal linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:15109702 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:12445206 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20230601 MGI PMID:17807638 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:5559839 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20160114 MGI PMID:25477496 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:6696991 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0006159 ocular albinism IAGP N RGD:5509061 20141003 MGI PMID:18715234 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:6696991 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20160114 MGI PMID:25477496 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20141003 MGI PMID:6696991 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20160114 MGI PMID:25477496 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0009557 decreased platelet ADP level IAGP N RGD:5509061 20141003 MGI PMID:6696991 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8441253 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:3711636 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0010192 abnormal retina melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7089489 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0010898 abnormal pulmonary alveolus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8441253 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:3711636 1320976 Bloc1s6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170720 MGI PMID:6696991 1320977 Elapor1 endosome-lysosome associated apoptosis and autophagy regulator 1 gene MP:0001156 abnormal spermatogenesis IEA N RGD:5509061 20170323 MGI 1320977 Elapor1 endosome-lysosome associated apoptosis and autophagy regulator 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1320977 Elapor1 endosome-lysosome associated apoptosis and autophagy regulator 1 gene MP:0001925 male infertility IEA N RGD:5509061 20170323 MGI 1320977 Elapor1 endosome-lysosome associated apoptosis and autophagy regulator 1 gene MP:0002687 oligozoospermia IEA N RGD:5509061 20170323 MGI 1320977 Elapor1 endosome-lysosome associated apoptosis and autophagy regulator 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20201022 MGI 1320977 Elapor1 endosome-lysosome associated apoptosis and autophagy regulator 1 gene MP:0002764 short tibia IEA N RGD:5509061 20201022 MGI 1320977 Elapor1 endosome-lysosome associated apoptosis and autophagy regulator 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201022 MGI 1320977 Elapor1 endosome-lysosome associated apoptosis and autophagy regulator 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 1320977 Elapor1 endosome-lysosome associated apoptosis and autophagy regulator 1 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20211021 MGI 1320977 Elapor1 endosome-lysosome associated apoptosis and autophagy regulator 1 gene MP:0005578 teratozoospermia IEA N RGD:5509061 20170323 MGI 1320977 Elapor1 endosome-lysosome associated apoptosis and autophagy regulator 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201022 MGI 1320977 Elapor1 endosome-lysosome associated apoptosis and autophagy regulator 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1320977 Elapor1 endosome-lysosome associated apoptosis and autophagy regulator 1 gene MP:0011941 increased fluid intake IEA N RGD:5509061 20210128 MGI 1320979 Ugp2 UDP-glucose pyrophosphorylase 2 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1320979 Ugp2 UDP-glucose pyrophosphorylase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1320983 Orai2 ORAI calcium release-activated calcium modulator 2 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20170921 MGI PMID:28294127 1320983 Orai2 ORAI calcium release-activated calcium modulator 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20170921 MGI PMID:28294127 1320983 Orai2 ORAI calcium release-activated calcium modulator 2 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20190919 MGI PMID:29604961 1320983 Orai2 ORAI calcium release-activated calcium modulator 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20170921 MGI PMID:28294127 1320983 Orai2 ORAI calcium release-activated calcium modulator 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20170921 MGI PMID:28294127 1320983 Orai2 ORAI calcium release-activated calcium modulator 2 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20170921 MGI PMID:28294127 1320983 Orai2 ORAI calcium release-activated calcium modulator 2 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20190919 MGI PMID:29604961 1320983 Orai2 ORAI calcium release-activated calcium modulator 2 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20170921 MGI PMID:28294127 1320983 Orai2 ORAI calcium release-activated calcium modulator 2 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20170921 MGI PMID:28294127 1320983 Orai2 ORAI calcium release-activated calcium modulator 2 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20170921 MGI PMID:28294127 1320983 Orai2 ORAI calcium release-activated calcium modulator 2 gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20190919 MGI PMID:29604961 1320983 Orai2 ORAI calcium release-activated calcium modulator 2 gene MP:0010183 abnormal CD4-positive helper T cell morphology IAGP N RGD:5509061 20170921 MGI PMID:28294127 1320988 Smtn smoothelin gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:16285958 1320988 Smtn smoothelin gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18678771 1320988 Smtn smoothelin gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:18678771 1320988 Smtn smoothelin gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:16285958 1320988 Smtn smoothelin gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16285958 1320988 Smtn smoothelin gene MP:0001262 decreased body weight IEA N RGD:5509061 20180222 MGI 1320988 Smtn smoothelin gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18678771 1320988 Smtn smoothelin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16285958 1320988 Smtn smoothelin gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:16285958 1320988 Smtn smoothelin gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:16285958 1320988 Smtn smoothelin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16285958 1320988 Smtn smoothelin gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18678771 1320988 Smtn smoothelin gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:18678771 1320988 Smtn smoothelin gene MP:0003262 intestinal/bowel diverticulum IAGP N RGD:5509061 20141003 MGI PMID:16285958 1320988 Smtn smoothelin gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:16285958 1320988 Smtn smoothelin gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:18678771 1320988 Smtn smoothelin gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20141003 MGI PMID:16285958 1320988 Smtn smoothelin gene MP:0004006 impaired contractility of jejunal smooth muscle IAGP N RGD:5509061 20141003 MGI PMID:16285958 1320988 Smtn smoothelin gene MP:0004857 abnormal heart weight IAGP N RGD:5509061 20141003 MGI PMID:18678771 1320988 Smtn smoothelin gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18678771 1320988 Smtn smoothelin gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:16285958 1320988 Smtn smoothelin gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:16285958 1320988 Smtn smoothelin gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:16285958 1320988 Smtn smoothelin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16285958 1320988 Smtn smoothelin gene MP:0011881 distended duodenum IAGP N RGD:5509061 20150702 MGI PMID:16285958 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20160811 MGI PMID:25848754 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0000929 open neural tube IAGP N RGD:5509061 20160811 MGI PMID:25848754 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20160811 MGI PMID:25848754 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160811 MGI PMID:25848754 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20160811 MGI PMID:25848754 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20160811 MGI PMID:27252784 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0010715 retina coloboma IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160811 MGI PMID:25848754 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160811 MGI PMID:27252784 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0012091 increased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0012265 increased hindbrain size IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0012535 abnormal optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0012678 absent fourth ventricle IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0013000 absent cerebral aqueduct IAGP N RGD:5509061 20141003 MGI PMID:21220025 1320990 Kdm2b lysine (K)-specific demethylase 2B gene MP:0013199 increased head mesenchyme apoptosis IAGP N RGD:5509061 20160428 MGI PMID:21220025 1320994 Cryzl1 crystallin zeta like 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0000066 osteoporosis IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0011585 decreased alkaline phosphatase activity IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320996 Atp6v1h ATPase, H+ transporting, lysosomal V1 subunit H gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20170330 MGI PMID:27924156 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:8999798 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:15919816 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19409815 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:8999798 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20152175 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:20152175 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20190502 MGI 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:8999798 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:8999798 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12077299 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15919816 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8999798 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12077299 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17023430 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:14528298 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18084302 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:18084302 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15919816 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:15919816 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15919816 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:19409815 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19409815 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19409815 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:14528298 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:14528298 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:19409815 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19409815 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19409815 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19409815 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0008176 abnormal germinal center B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21642988 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21642988 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17023430 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19409815 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21642988 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:14528298 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12077299 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15919816 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20152175 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8999798 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15919816 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:15919816 1320998 Gna13 guanine nucleotide binding protein, alpha 13 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1321000 Ifrd2 interferon-related developmental regulator 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240627 MGI PMID:37603466 1321000 Ifrd2 interferon-related developmental regulator 2 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20240627 MGI PMID:37603466 1321000 Ifrd2 interferon-related developmental regulator 2 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20240627 MGI PMID:37603466 1321000 Ifrd2 interferon-related developmental regulator 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20240627 MGI PMID:37603466 1321000 Ifrd2 interferon-related developmental regulator 2 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20240627 MGI PMID:37603466 1321000 Ifrd2 interferon-related developmental regulator 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20240627 MGI PMID:37603466 1321000 Ifrd2 interferon-related developmental regulator 2 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20240627 MGI PMID:37603466 1321000 Ifrd2 interferon-related developmental regulator 2 gene MP:0011169 abnormal white fat cell differentation IAGP N RGD:5509061 20240627 MGI PMID:37603466 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0010332 abnormal circulating apolipoprotein level IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20170216 MGI PMID:25806685 1321001 Lpcat3 lysophosphatidylcholine acyltransferase 3 gene MP:0021045 decreased circulating VLDL phospholipid level IAGP N RGD:5509061 20220106 MGI PMID:25806685 1321002 Eci3 enoyl-Coenzyme A delta isomerase 3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1321006 Frs3 fibroblast growth factor receptor substrate 3 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20180301 MGI PMID:28483978 1321006 Frs3 fibroblast growth factor receptor substrate 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20180301 MGI PMID:28483978 1321006 Frs3 fibroblast growth factor receptor substrate 3 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20180301 MGI PMID:28483978 1321006 Frs3 fibroblast growth factor receptor substrate 3 gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20180301 MGI PMID:28483978 1321006 Frs3 fibroblast growth factor receptor substrate 3 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20180301 MGI PMID:28483978 1321006 Frs3 fibroblast growth factor receptor substrate 3 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20180301 MGI PMID:28483978 1321006 Frs3 fibroblast growth factor receptor substrate 3 gene MP:0012556 increased cell death IAGP N RGD:5509061 20180301 MGI PMID:28483978 1321006 Frs3 fibroblast growth factor receptor substrate 3 gene MP:0012683 absent telencephalon IAGP N RGD:5509061 20180301 MGI PMID:28483978 1321006 Frs3 fibroblast growth factor receptor substrate 3 gene MP:0030250 frontonasal prominence hypoplasia IAGP N RGD:5509061 20180301 MGI PMID:28483978 1321012 Mff mitochondrial fission factor gene MP:0001657 abnormal induced morbidity/mortality IAGP N RGD:5509061 20180524 MGI PMID:28288978 1321012 Mff mitochondrial fission factor gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220428 MGI PMID:33476744 1321012 Mff mitochondrial fission factor gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20180524 MGI PMID:28288978 1321012 Mff mitochondrial fission factor gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20220428 MGI PMID:33476744 1321012 Mff mitochondrial fission factor gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20180524 MGI PMID:28288978 1321012 Mff mitochondrial fission factor gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220428 MGI PMID:33476744 1321012 Mff mitochondrial fission factor gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220428 MGI PMID:33476744 1321012 Mff mitochondrial fission factor gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220428 MGI PMID:33476744 1321012 Mff mitochondrial fission factor gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20220428 MGI PMID:33476744 1321012 Mff mitochondrial fission factor gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220428 MGI PMID:33476744 1321012 Mff mitochondrial fission factor gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220428 MGI PMID:33476744 1321012 Mff mitochondrial fission factor gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20220428 MGI PMID:33476744 1321012 Mff mitochondrial fission factor gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20220428 MGI PMID:33476744 1321012 Mff mitochondrial fission factor gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20220428 MGI PMID:33476744 1321012 Mff mitochondrial fission factor gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20220428 MGI PMID:33476744 1321012 Mff mitochondrial fission factor gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20220428 MGI PMID:33476744 1321012 Mff mitochondrial fission factor gene MP:0014467 increased sperm mitochondrial size IAGP N RGD:5509061 20240613 MGI PMID:33476744 1321016 Ap4m1 adaptor-related protein complex AP-4, mu 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1321016 Ap4m1 adaptor-related protein complex AP-4, mu 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20201022 MGI 1321016 Ap4m1 adaptor-related protein complex AP-4, mu 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1321016 Ap4m1 adaptor-related protein complex AP-4, mu 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1321016 Ap4m1 adaptor-related protein complex AP-4, mu 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1321016 Ap4m1 adaptor-related protein complex AP-4, mu 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20210128 MGI 1321016 Ap4m1 adaptor-related protein complex AP-4, mu 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1321016 Ap4m1 adaptor-related protein complex AP-4, mu 1 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1321020 Gabpb1 GA repeat binding protein, beta 1 gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:18426908 1321020 Gabpb1 GA repeat binding protein, beta 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18426908 1321022 Prkd3 protein kinase D3 gene MP:0000130 abnormal trabecular bone morphology IEA N RGD:5509061 20111116 MGI 1321022 Prkd3 protein kinase D3 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20111116 MGI 1321022 Prkd3 protein kinase D3 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20221215 MGI 1321022 Prkd3 protein kinase D3 gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20111116 MGI 1321022 Prkd3 protein kinase D3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20161117 MGI PMID:27670070 1321022 Prkd3 protein kinase D3 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20161117 MGI PMID:27670070 1321022 Prkd3 protein kinase D3 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20221215 MGI 1321022 Prkd3 protein kinase D3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1321022 Prkd3 protein kinase D3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1321022 Prkd3 protein kinase D3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210520 MGI 1321022 Prkd3 protein kinase D3 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20240523 MGI 1321022 Prkd3 protein kinase D3 gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20161117 MGI PMID:27670070 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16754854 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11778047 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12417422 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11778047 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12417422 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11778047 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12417422 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:16754854 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:16754854 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16754854 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11778047 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12417422 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16754854 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16754854 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16754854 1321025 Man2a2 mannosidase 2, alpha 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16754854 1321027 Gp1ba glycoprotein 1b, alpha polypeptide gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:10706630 1321027 Gp1ba glycoprotein 1b, alpha polypeptide gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:10706630 1321027 Gp1ba glycoprotein 1b, alpha polypeptide gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17382885 1321027 Gp1ba glycoprotein 1b, alpha polypeptide gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:10706630 1321027 Gp1ba glycoprotein 1b, alpha polypeptide gene MP:0030025 giant platelets IAGP N RGD:5509061 20170803 MGI PMID:10706630 1321028 Mettl2 methyltransferase 2, methylcytidine gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20170713 MGI PMID:28655767 1321034 Ccl24 C-C motif chemokine ligand 24 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:15647285 1321034 Ccl24 C-C motif chemokine ligand 24 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:16210640 1321034 Ccl24 C-C motif chemokine ligand 24 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16210640 1321034 Ccl24 C-C motif chemokine ligand 24 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:17060636 1321034 Ccl24 C-C motif chemokine ligand 24 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17060636 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23173044 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23173044 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21841312 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23173044 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:21841312 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:23173044 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21841312 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:21841312 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:21841312 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21841312 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21841312 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23173044 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21841312 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23173044 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23173044 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0009287 decreased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23173044 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23173044 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23173044 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:23173044 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0031414 decreased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:23173044 1321036 Cdkal1 CDK5 regulatory subunit associated protein 1-like 1 gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:23173044 1321039 Msgn1 mesogenin 1 gene MP:0000138 absent vertebrae IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0000151 absent ribs IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0000962 disorganized dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0003401 enlarged tail bud IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0004197 abnormal fetal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0012182 abnormal presomitic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0012184 absent paraxial mesoderm IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0012277 increased tail bud apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321039 Msgn1 mesogenin 1 gene MP:0012707 incomplete caudal neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:11124811 1321042 Mzb1 marginal zone B and B1 cell-specific protein 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20190509 MGI PMID:24888588 1321042 Mzb1 marginal zone B and B1 cell-specific protein 1 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20190509 MGI PMID:24888588 1321042 Mzb1 marginal zone B and B1 cell-specific protein 1 gene MP:0003134 increased late pro-B cell number IAGP N RGD:5509061 20190509 MGI PMID:24888588 1321042 Mzb1 marginal zone B and B1 cell-specific protein 1 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220519 MGI 1321042 Mzb1 marginal zone B and B1 cell-specific protein 1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20240523 MGI 1321042 Mzb1 marginal zone B and B1 cell-specific protein 1 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20240523 MGI 1321042 Mzb1 marginal zone B and B1 cell-specific protein 1 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20190509 MGI PMID:24888588 1321042 Mzb1 marginal zone B and B1 cell-specific protein 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20190509 MGI PMID:24888588 1321042 Mzb1 marginal zone B and B1 cell-specific protein 1 gene MP:0009198 abnormal male genitalia morphology IEA N RGD:5509061 20230720 MGI 1321042 Mzb1 marginal zone B and B1 cell-specific protein 1 gene MP:0009208 abnormal female genitalia morphology IEA N RGD:5509061 20240523 MGI 1321042 Mzb1 marginal zone B and B1 cell-specific protein 1 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20190509 MGI PMID:24888588 1321042 Mzb1 marginal zone B and B1 cell-specific protein 1 gene MP:0020154 impaired humoral immune response IAGP N RGD:5509061 20190509 MGI PMID:24888588 1321044 Ano4 anoctamin 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1321044 Ano4 anoctamin 4 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 1321044 Ano4 anoctamin 4 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 1321048 Tbc1d5 TBC1 domain family, member 5 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20240523 MGI 1321048 Tbc1d5 TBC1 domain family, member 5 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201022 MGI 1321048 Tbc1d5 TBC1 domain family, member 5 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1321048 Tbc1d5 TBC1 domain family, member 5 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1321050 Col9a3 collagen, type IX, alpha 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200514 MGI 1321050 Col9a3 collagen, type IX, alpha 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20200514 MGI 1321050 Col9a3 collagen, type IX, alpha 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1321050 Col9a3 collagen, type IX, alpha 3 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20220811 MGI 1321050 Col9a3 collagen, type IX, alpha 3 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20200514 MGI 1321050 Col9a3 collagen, type IX, alpha 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:11058094 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:15537701 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:7310489 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7310489 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:7310489 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20210729 MGI PMID:32016796 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10193444 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:10193444 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:9434937 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:9434937 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11058094 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0001386 abnormal maternal nurturing IEA N RGD:5509061 20111116 MGI 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0001389 abnormal eye movement IAGP N RGD:5509061 20141003 MGI PMID:7310489 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12777251 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0001926 female infertility IEA N RGD:5509061 20111116 MGI 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0001935 decreased litter size IAGP N RGD:5509061 20210729 MGI PMID:32016796 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:12777251 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:6279728 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0002082 postnatal lethality IEA N RGD:5509061 20111116 MGI 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10193444 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:7310489 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0002095 abnormal skin pigmentation IEA N RGD:5509061 20111116 MGI 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:10193444 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12777251 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:12777251 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:6696991 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0002620 abnormal monocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12777251 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0002637 small uterus IAGP N RGD:5509061 20210729 MGI PMID:32016796 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0002938 white spotting IEA N RGD:5509061 20111116 MGI 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0003173 decreased lysosomal enzyme secretion IAGP N RGD:5509061 20141003 MGI PMID:6696991 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15537701 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0004165 abnormal lateral geniculate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:7310489 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0004267 abnormal optic tract morphology IAGP N RGD:5509061 20141003 MGI PMID:3584547 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0004721 abnormal platelet dense granule morphology IAGP N RGD:5509061 20141003 MGI PMID:10381507 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:6696991 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:115747 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:10381507 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:11058094 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0005060 accumulation of giant lysosomes in kidney/renal tubule cells IAGP N RGD:5509061 20141003 MGI PMID:10381507 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:11058094 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:12445206 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9434937 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:115747 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:15537701 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:9434937 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20160114 MGI PMID:25477496 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:11058094 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:6696991 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:12777251 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0005636 abnormal mineral homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11058094 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0006103 abnormal midbrain roof plate morphology IAGP N RGD:5509061 20141003 MGI PMID:3584547 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20160114 MGI PMID:25477496 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12777251 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0008028 pregnancy-related premature death IEA N RGD:5509061 20111116 MGI 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0008258 thin endometrium IAGP N RGD:5509061 20210729 MGI PMID:32016796 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0009088 thin uterine horn IAGP N RGD:5509061 20210729 MGI PMID:32016796 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0009089 short uterine horn IAGP N RGD:5509061 20210729 MGI PMID:32016796 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0009379 abnormal foot pigmentation IEA N RGD:5509061 20111116 MGI 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20141003 MGI PMID:6696991 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20141003 MGI PMID:9434937 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20141003 MGI PMID:6696991 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20141003 MGI PMID:9434937 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:9434937 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20160114 MGI PMID:25477496 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0009557 decreased platelet ADP level IAGP N RGD:5509061 20141003 MGI PMID:6696991 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0009557 decreased platelet ADP level IAGP N RGD:5509061 20141003 MGI PMID:9434937 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0010815 enlarged alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:12777251 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0010950 abnormal lung hysteresivity IAGP N RGD:5509061 20141003 MGI PMID:12777251 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0011088 neonatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0011277 decreased tail pigmentation IEA N RGD:5509061 20111116 MGI 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0011279 decreased ear pigmentation IEA N RGD:5509061 20111116 MGI 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170720 MGI PMID:6696991 1321052 Ap3b1 adaptor-related protein complex 3, beta 1 subunit gene MP:0020916 increased susceptibility to Herpesvirales infection IEA N RGD:5509061 20200430 MGI 1321055 E2f7 E2F transcription factor 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18194653 1321055 E2f7 E2F transcription factor 7 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18194653 1321055 E2f7 E2F transcription factor 7 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18194653 1321055 E2f7 E2F transcription factor 7 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18194653 1321055 E2f7 E2F transcription factor 7 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18194653 1321055 E2f7 E2F transcription factor 7 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18194653 1321055 E2f7 E2F transcription factor 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18194653 1321055 E2f7 E2F transcription factor 7 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0008402 increased cellular sensitivity to alkylating agents IAGP N RGD:5509061 20141003 MGI PMID:18194653 1321055 E2f7 E2F transcription factor 7 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0008959 abnormal spongiotrophoblast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0009658 increased placenta apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18194653 1321055 E2f7 E2F transcription factor 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22516201 1321055 E2f7 E2F transcription factor 7 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150219 MGI PMID:18194653 1321060 Nhlh1 nescient helix loop helix 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1321060 Nhlh1 nescient helix loop helix 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:12077327 1321060 Nhlh1 nescient helix loop helix 1 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:12077327 1321060 Nhlh1 nescient helix loop helix 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12077327 1321060 Nhlh1 nescient helix loop helix 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15470499 1321060 Nhlh1 nescient helix loop helix 1 gene MP:0003929 decreased heart rate variability IAGP N RGD:5509061 20141003 MGI PMID:12077327 1321060 Nhlh1 nescient helix loop helix 1 gene MP:0004156 abnormal QT variability IAGP N RGD:5509061 20141003 MGI PMID:12077327 1321060 Nhlh1 nescient helix loop helix 1 gene MP:0006110 ventricular fibrillation IAGP N RGD:5509061 20141003 MGI PMID:12077327 1321060 Nhlh1 nescient helix loop helix 1 gene MP:0006277 abnormal parasympathetic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12077327 1321060 Nhlh1 nescient helix loop helix 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:15470499 1321060 Nhlh1 nescient helix loop helix 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1321060 Nhlh1 nescient helix loop helix 1 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20141003 MGI PMID:12077327 1321060 Nhlh1 nescient helix loop helix 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20210826 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210826 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0002188 small heart IEA N RGD:5509061 20210826 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0002637 small uterus IEA N RGD:5509061 20210826 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18511420 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0009456 impaired cued conditioning behavior IEA N RGD:5509061 20201022 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20181227 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1321063 G2e3 G2/M-phase specific E3 ubiquitin ligase gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18511420 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0001925 male infertility IAGP N RGD:5509061 20200618 MGI PMID:30415212 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0001925 male infertility IAGP N RGD:5509061 20220224 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220224 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220224 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20171116 MGI PMID:28495971 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20200618 MGI PMID:30415212 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20220224 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20200618 MGI PMID:30415212 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220224 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20200618 MGI PMID:30415212 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20200618 MGI PMID:30415212 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220224 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20200618 MGI PMID:30415212 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20200618 MGI PMID:30415212 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220224 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20220224 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220224 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220224 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20220224 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20200618 MGI PMID:30415212 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220224 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20171116 MGI PMID:28495971 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20200618 MGI PMID:30415212 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220224 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20220224 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0030591 absent sperm fibrous sheath IAGP N RGD:5509061 20220224 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220317 MGI PMID:29606301 1321066 Cfap69 cilia and flagella associated protein 69 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220811 MGI PMID:30415212 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15181535 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000040 absent middle ear ossicles IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11967920 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:14975718 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:11967920 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000088 short mandible IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:11967920 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14975718 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19855134 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000111 cleft palate IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:14975718 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000158 absent sternum IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000158 absent sternum IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11967920 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:14975718 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:15181535 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000450 absent snout IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000453 absent mouth IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000553 absent radius IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000553 absent radius IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:17984226 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000562 polydactyly IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:19855134 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11967920 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000914 exencephaly IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000919 cranioschisis IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11967920 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:15198977 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001062 absent oculomotor nerve IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001072 abnormal vestibulocochlear nerve morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001288 abnormal lens induction IAGP N RGD:5509061 20141003 MGI PMID:17428831 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001288 abnormal lens induction IAGP N RGD:5509061 20141003 MGI PMID:9918694 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:9918694 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:9918694 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:14975718 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:15181535 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:9918694 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:15181535 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:17428831 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:9918694 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:9918694 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:15181535 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001341 absent eyelids IAGP N RGD:5509061 20141003 MGI PMID:9918694 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:11967920 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:15181535 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:14975718 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16672719 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20141003 MGI PMID:12438097 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19855134 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16672719 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16672719 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:19855134 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0003104 acrania IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0003388 absent pericardium IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0003395 abnormal subclavian artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:19855134 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20221027 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:9918694 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004339 absent clavicle IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004377 small frontal bone IAGP N RGD:5509061 20141003 MGI PMID:11967920 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004379 wide frontal bone IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004380 short frontal bone IAGP N RGD:5509061 20141003 MGI PMID:14975718 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004380 short frontal bone IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004383 absent interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:11967920 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004383 absent interparietal bone IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:15181535 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004419 absent parietal bone IAGP N RGD:5509061 20141003 MGI PMID:11967920 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004468 small zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:11967920 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:14975718 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004472 broad nasal bone IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20141003 MGI PMID:11967920 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004539 absent maxilla IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004673 splayed ribs IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20141003 MGI PMID:15181535 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0004838 abnormal neural fold elevation formation IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11967920 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15181535 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:15181535 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:15181535 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0005174 abnormal tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9918694 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0005261 aniridia IAGP N RGD:5509061 20141003 MGI PMID:9918694 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:19855134 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0006130 pulmonary valve atresia IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0006211 small orbits IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0006306 abnormal nasal pit morphology IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:15181535 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0008510 absent retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:9918694 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0008797 facial cleft IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0009379 abnormal foot pigmentation IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0009844 abnormal neural crest cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0009893 cleft primary palate IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0010043 abnormal frontonasal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:14975718 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0010043 abnormal frontonasal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0010224 abnormal heart ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0010241 abnormal aortic arch development IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19855134 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:19855134 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0010572 persistent right dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15181535 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8622765 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8622766 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16672719 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:11744375 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0012535 abnormal optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:9918694 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0012747 abnormal cardiac neural crest cell morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0013550 abnormal secondary palate morphology IAGP N RGD:5509061 20150827 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:15181535 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0021211 unilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20170928 MGI PMID:25381013 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0030191 narrow snout IAGP N RGD:5509061 20171019 MGI PMID:15181535 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0030200 abnormal nasal septum cartilage morphology IAGP N RGD:5509061 20171012 MGI PMID:14975718 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0030334 absent sixth pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0030337 enlarged third pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0030340 absent fourth pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0030341 fourth pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20171116 MGI PMID:14623825 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0030341 fourth pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20171116 MGI PMID:19855134 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0030531 abnormal facial skin morphology IAGP N RGD:5509061 20180118 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0030532 abnormal periorbital skin morphology IAGP N RGD:5509061 20180118 MGI PMID:14975722 1321068 Tfap2a transcription factor AP-2, alpha gene MP:0030579 thoracoabdominoschisis IAGP N RGD:5509061 20180607 MGI PMID:8622766 1321070 Thap11 THAP domain containing 11 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20220217 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0000373 belly spot IAGP N RGD:5509061 20220217 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0000562 polydactyly IAGP N RGD:5509061 20220721 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0000585 kinked tail IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0000914 exencephaly IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0001575 cyanosis IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20220217 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20220217 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18585351 1321070 Thap11 THAP domain containing 11 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20220210 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20220217 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18585351 1321070 Thap11 THAP domain containing 11 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20220217 MGI PMID:35013307 1321070 Thap11 THAP domain containing 11 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:18585351 1321070 Thap11 THAP domain containing 11 gene MP:0030930 decreased digit pigmentation IAGP N RGD:5509061 20220721 MGI PMID:35013307 1321072 Mettl25 methyltransferase like 25 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20220519 MGI 1321072 Mettl25 methyltransferase like 25 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1321075 Pkd2l2 polycystic kidney disease 2-like 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1321075 Pkd2l2 polycystic kidney disease 2-like 2 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20220421 MGI 1321075 Pkd2l2 polycystic kidney disease 2-like 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1321075 Pkd2l2 polycystic kidney disease 2-like 2 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1321075 Pkd2l2 polycystic kidney disease 2-like 2 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20211021 MGI 1321075 Pkd2l2 polycystic kidney disease 2-like 2 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1321075 Pkd2l2 polycystic kidney disease 2-like 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1321075 Pkd2l2 polycystic kidney disease 2-like 2 gene MP:0031391 increased locomotor activity IEA N RGD:5509061 20220421 MGI 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210128 MGI 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321077 Mark4 MAP/microtubule affinity regulating kinase 4 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:22992738 1321079 Clk4 CDC like kinase 4 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20220915 MGI PMID:35907876 1321079 Clk4 CDC like kinase 4 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20220915 MGI PMID:35907876 1321079 Clk4 CDC like kinase 4 gene MP:0004093 diffuse Z line IAGP N RGD:5509061 20220915 MGI PMID:35907876 1321079 Clk4 CDC like kinase 4 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20220915 MGI PMID:35907876 1321079 Clk4 CDC like kinase 4 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20220915 MGI PMID:35907876 1321079 Clk4 CDC like kinase 4 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20220915 MGI PMID:35907876 1321079 Clk4 CDC like kinase 4 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20220915 MGI PMID:35907876 1321079 Clk4 CDC like kinase 4 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20220915 MGI PMID:35907876 1321079 Clk4 CDC like kinase 4 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20220915 MGI PMID:35907876 1321079 Clk4 CDC like kinase 4 gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20220915 MGI PMID:35907876 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:17981124 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20457756 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:20457756 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:15923632 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:17981124 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:20457756 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:20457756 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:20457756 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17981124 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20457756 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0001856 myocarditis IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15020257 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20457756 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20200618 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20170504 MGI PMID:26389676 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20170504 MGI PMID:26389676 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0002869 increased anti-insulin autoantibody level IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17981124 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20170504 MGI PMID:26389676 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20457756 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20457756 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20170504 MGI PMID:26389676 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17981124 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0003858 enhanced coordination IEA N RGD:5509061 20141003 MGI 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:17981124 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20170504 MGI PMID:26389676 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0005563 abnormal hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20457756 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:20457756 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0008112 abnormal monocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:20457756 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15923632 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:17981124 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20457756 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0009488 abnormal pancreatic islet cell apoptosis IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20457756 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18219322 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15923632 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20457756 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17981124 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20160225 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0014117 increased pancreatic beta cell apoptosis IAGP N RGD:5509061 20160324 MGI PMID:26596471 1321081 Senp1 SUMO1/sentrin specific peptidase 1 gene MP:0031059 increased circulating C-reactive protein level IAGP N RGD:5509061 20200618 MGI PMID:26596471 1321087 Mccc2 methylcrotonoyl-Coenzyme A carboxylase 2 (beta) gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20201022 MGI 1321087 Mccc2 methylcrotonoyl-Coenzyme A carboxylase 2 (beta) gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1321087 Mccc2 methylcrotonoyl-Coenzyme A carboxylase 2 (beta) gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1321087 Mccc2 methylcrotonoyl-Coenzyme A carboxylase 2 (beta) gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1321087 Mccc2 methylcrotonoyl-Coenzyme A carboxylase 2 (beta) gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20221215 MGI 1321087 Mccc2 methylcrotonoyl-Coenzyme A carboxylase 2 (beta) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321090 C2cd2l C2 calcium-dependent domain containing 2-like gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1321090 C2cd2l C2 calcium-dependent domain containing 2-like gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210128 MGI 1321090 C2cd2l C2 calcium-dependent domain containing 2-like gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1321092 Ehf ets homologous factor gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20231207 MGI 1321092 Ehf ets homologous factor gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20191107 MGI PMID:30224759 1321092 Ehf ets homologous factor gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 1321092 Ehf ets homologous factor gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20231207 MGI 1321092 Ehf ets homologous factor gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20191107 MGI PMID:30224759 1321092 Ehf ets homologous factor gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20231207 MGI 1321092 Ehf ets homologous factor gene MP:0005505 thrombocytosis IEA N RGD:5509061 20231207 MGI 1321092 Ehf ets homologous factor gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20191107 MGI PMID:30224759 1321092 Ehf ets homologous factor gene MP:0012734 abnormal response to radiation IAGP N RGD:5509061 20191107 MGI PMID:30224759 1321092 Ehf ets homologous factor gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20231207 MGI 1321098 Adgrf1 adhesion G protein-coupled receptor F1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240523 MGI 1321098 Adgrf1 adhesion G protein-coupled receptor F1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20240523 MGI 1321098 Adgrf1 adhesion G protein-coupled receptor F1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1321098 Adgrf1 adhesion G protein-coupled receptor F1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 1321098 Adgrf1 adhesion G protein-coupled receptor F1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1321098 Adgrf1 adhesion G protein-coupled receptor F1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1321101 Zbtb43 zinc finger and BTB domain containing 43 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20231207 MGI 1321101 Zbtb43 zinc finger and BTB domain containing 43 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1321101 Zbtb43 zinc finger and BTB domain containing 43 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1321101 Zbtb43 zinc finger and BTB domain containing 43 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1321101 Zbtb43 zinc finger and BTB domain containing 43 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1321101 Zbtb43 zinc finger and BTB domain containing 43 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20240523 MGI 1321101 Zbtb43 zinc finger and BTB domain containing 43 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20181227 MGI 1321101 Zbtb43 zinc finger and BTB domain containing 43 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1321101 Zbtb43 zinc finger and BTB domain containing 43 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1321101 Zbtb43 zinc finger and BTB domain containing 43 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1321101 Zbtb43 zinc finger and BTB domain containing 43 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20181227 MGI 1321101 Zbtb43 zinc finger and BTB domain containing 43 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1321103 Pcdhb13 protocadherin beta 13 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210128 MGI 1321103 Pcdhb13 protocadherin beta 13 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1321103 Pcdhb13 protocadherin beta 13 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1321103 Pcdhb13 protocadherin beta 13 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1321103 Pcdhb13 protocadherin beta 13 gene MP:0002607 decreased basophil cell number IEA N RGD:5509061 20221215 MGI 1321103 Pcdhb13 protocadherin beta 13 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1321103 Pcdhb13 protocadherin beta 13 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210128 MGI 1321105 Psd4 pleckstrin and Sec7 domain containing 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16103131 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:16103131 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16103131 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22914734 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:22914734 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22914734 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160623 MGI PMID:27038906 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16103131 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16103131 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160623 MGI PMID:27038906 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22914734 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160623 MGI PMID:27038906 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20160623 MGI PMID:27038906 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16103131 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22914734 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:22914734 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22914734 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20160623 MGI PMID:27038906 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:22914734 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20160623 MGI PMID:27038906 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:22914734 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:22914734 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:16103131 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22914734 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0004167 abnormal cingulate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:22914734 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:16103131 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:22914734 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20160623 MGI PMID:27038906 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:22914734 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20160623 MGI PMID:27038906 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20160623 MGI PMID:27038906 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0008918 microgliosis IAGP N RGD:5509061 20160623 MGI PMID:27038906 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:16103131 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0010009 abnormal piriform cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22914734 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20160623 MGI PMID:27038906 1321107 Cox10 heme A:farnesyltransferase cytochrome c oxidase assembly factor 10 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:27038906 1321109 Snx2 sorting nexin 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:16214895 1321109 Snx2 sorting nexin 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16214895 1321109 Snx2 sorting nexin 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:12388759 1321109 Snx2 sorting nexin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12388759 1321109 Snx2 sorting nexin 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12388759 1321109 Snx2 sorting nexin 2 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12388759 1321109 Snx2 sorting nexin 2 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:12388759 1321109 Snx2 sorting nexin 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12388759 1321109 Snx2 sorting nexin 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16214895 1321109 Snx2 sorting nexin 2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12388759 1321109 Snx2 sorting nexin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12388759 1321109 Snx2 sorting nexin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16214895 1321109 Snx2 sorting nexin 2 gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12388759 1321109 Snx2 sorting nexin 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12388759 1321109 Snx2 sorting nexin 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16214895 1321109 Snx2 sorting nexin 2 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:12388759 1321109 Snx2 sorting nexin 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16214895 1321109 Snx2 sorting nexin 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12388759 1321109 Snx2 sorting nexin 2 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16214895 1321109 Snx2 sorting nexin 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12388759 1321109 Snx2 sorting nexin 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16214895 1321109 Snx2 sorting nexin 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16214895 1321109 Snx2 sorting nexin 2 gene MP:0020515 abnormal visceral yolk sac endoderm morphology IAGP N RGD:5509061 20180125 MGI PMID:12388759 1321110 Bicdl1 BICD family like cargo adaptor 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1321110 Bicdl1 BICD family like cargo adaptor 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20190502 MGI 1321110 Bicdl1 BICD family like cargo adaptor 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1321110 Bicdl1 BICD family like cargo adaptor 1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20161201 MGI 1321110 Bicdl1 BICD family like cargo adaptor 1 gene MP:0002764 short tibia IEA N RGD:5509061 20161201 MGI 1321110 Bicdl1 BICD family like cargo adaptor 1 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20211021 MGI 1321110 Bicdl1 BICD family like cargo adaptor 1 gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20211021 MGI 1321110 Bicdl1 BICD family like cargo adaptor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20371609 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:17928865 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18347093 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20210520 MGI 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:17928865 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17928865 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:17928865 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220519 MGI 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:20371609 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20210520 MGI 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210520 MGI 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:18347093 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20371609 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20371609 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210520 MGI 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0003948 abnormal gas homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:20371609 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:20371609 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0004892 increased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:17928865 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20371609 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:20371609 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:20371609 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:20371609 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:20371609 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20141003 MGI PMID:17928865 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:20371609 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0009130 increased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:20371609 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:20371609 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19066220 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:17928865 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:17928865 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17928865 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18347093 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20371609 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17928865 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18347093 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0011747 myelofibrosis IAGP N RGD:5509061 20141003 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0031204 hindlimb paresis IAGP N RGD:5509061 20210218 MGI PMID:24191050 1321112 Ncor2 nuclear receptor co-repressor 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:20371609 1321114 Perp PERP, TP53 apoptosis effector gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14614825 1321114 Perp PERP, TP53 apoptosis effector gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:14614825 1321114 Perp PERP, TP53 apoptosis effector gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:20975948 1321114 Perp PERP, TP53 apoptosis effector gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14614825 1321114 Perp PERP, TP53 apoptosis effector gene MP:0009581 decreased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20975948 1321114 Perp PERP, TP53 apoptosis effector gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20975948 1321114 Perp PERP, TP53 apoptosis effector gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:20975948 1321114 Perp PERP, TP53 apoptosis effector gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14614825 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20170706 MGI PMID:28162974 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210826 MGI 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20170706 MGI PMID:28162974 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220519 MGI 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20170706 MGI PMID:28162974 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0003344 mammary gland hypoplasia IAGP N RGD:5509061 20170706 MGI PMID:28162974 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20170706 MGI PMID:28162974 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20170706 MGI PMID:28162974 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20170706 MGI PMID:28162974 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20170706 MGI PMID:28162974 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0010052 increased grip strength IEA N RGD:5509061 20160811 MGI 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20170706 MGI PMID:28162974 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20170706 MGI PMID:28162974 1321118 Ube2o ubiquitin-conjugating enzyme E2O gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:28162974 1321120 Hoxb1 homeobox B1 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 1321120 Hoxb1 homeobox B1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:15861402 1321120 Hoxb1 homeobox B1 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:15198977 1321120 Hoxb1 homeobox B1 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:16890163 1321120 Hoxb1 homeobox B1 gene MP:0000843 absent facial nuclei IAGP N RGD:5509061 20141003 MGI PMID:16890163 1321120 Hoxb1 homeobox B1 gene MP:0000843 absent facial nuclei IAGP N RGD:5509061 20141003 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 1321120 Hoxb1 homeobox B1 gene MP:0000909 abnormal facial motor nucleus morphology IEA N RGD:5509061 20141003 MGI 1321120 Hoxb1 homeobox B1 gene MP:0000910 small facial motor nucleus IAGP N RGD:5509061 20141003 MGI PMID:16890163 1321120 Hoxb1 homeobox B1 gene MP:0000910 small facial motor nucleus IAGP N RGD:5509061 20141003 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:15198977 1321120 Hoxb1 homeobox B1 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:14960494 1321120 Hoxb1 homeobox B1 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15198977 1321120 Hoxb1 homeobox B1 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16890163 1321120 Hoxb1 homeobox B1 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:8967950 1321120 Hoxb1 homeobox B1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18155191 1321120 Hoxb1 homeobox B1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18155191 1321120 Hoxb1 homeobox B1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18155191 1321120 Hoxb1 homeobox B1 gene MP:0001490 abnormal vibrissae reflex IAGP N RGD:5509061 20141003 MGI PMID:15198977 1321120 Hoxb1 homeobox B1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:18155191 1321120 Hoxb1 homeobox B1 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:15198977 1321120 Hoxb1 homeobox B1 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:16890163 1321120 Hoxb1 homeobox B1 gene MP:0001993 abnormal blinking IAGP N RGD:5509061 20141003 MGI PMID:15198977 1321120 Hoxb1 homeobox B1 gene MP:0001993 abnormal blinking IAGP N RGD:5509061 20171005 MGI PMID:16890163 1321120 Hoxb1 homeobox B1 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12815623 1321120 Hoxb1 homeobox B1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15198977 1321120 Hoxb1 homeobox B1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16890163 1321120 Hoxb1 homeobox B1 gene MP:0002863 improved righting response IAGP N RGD:5509061 20141003 MGI PMID:18155191 1321120 Hoxb1 homeobox B1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18155191 1321120 Hoxb1 homeobox B1 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:11532923 1321120 Hoxb1 homeobox B1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:8967950 1321120 Hoxb1 homeobox B1 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:18155191 1321120 Hoxb1 homeobox B1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:15861402 1321120 Hoxb1 homeobox B1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:18155191 1321120 Hoxb1 homeobox B1 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0004235 abnormal masseter muscle morphology IAGP N RGD:5509061 20171005 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0004239 abnormal temporalis muscle morphology IAGP N RGD:5509061 20171005 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:18155191 1321120 Hoxb1 homeobox B1 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 1321120 Hoxb1 homeobox B1 gene MP:0004561 absent facial nerve IAGP N RGD:5509061 20141003 MGI PMID:16890163 1321120 Hoxb1 homeobox B1 gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:23408898 1321120 Hoxb1 homeobox B1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:18155191 1321120 Hoxb1 homeobox B1 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:18155191 1321120 Hoxb1 homeobox B1 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 1321120 Hoxb1 homeobox B1 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:18155191 1321120 Hoxb1 homeobox B1 gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:18155191 1321120 Hoxb1 homeobox B1 gene MP:0006334 abnormal susceptibility to hearing loss IAGP N RGD:5509061 20141003 MGI PMID:23408898 1321120 Hoxb1 homeobox B1 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0008372 small malleus IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:18155191 1321120 Hoxb1 homeobox B1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18155191 1321120 Hoxb1 homeobox B1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:8967950 1321120 Hoxb1 homeobox B1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16890163 1321120 Hoxb1 homeobox B1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8967950 1321120 Hoxb1 homeobox B1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23408898 1321120 Hoxb1 homeobox B1 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0012490 abnormal cochlear VIII nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 1321120 Hoxb1 homeobox B1 gene MP:0012524 abnormal lower lip morphology IAGP N RGD:5509061 20141003 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0012746 abnormal neural crest cell delamination IAGP N RGD:5509061 20141003 MGI PMID:11532923 1321120 Hoxb1 homeobox B1 gene MP:0012796 abnormal rhombomere 4 morphology IAGP N RGD:5509061 20141003 MGI PMID:8967950 1321120 Hoxb1 homeobox B1 gene MP:0012799 absent rhombomere 4 IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0012803 absent rhombomere 5 IAGP N RGD:5509061 20141003 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0013224 absent second pharyngeal pouch IAGP N RGD:5509061 20150101 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0013225 abnormal third pharyngeal pouch morphology IAGP N RGD:5509061 20150101 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0030040 absent facial muscle IAGP N RGD:5509061 20170921 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0030040 absent facial muscle IAGP N RGD:5509061 20170921 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0030067 narrow face IAGP N RGD:5509061 20170921 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0030106 small incus IAGP N RGD:5509061 20171005 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0030141 facial paralysis IAGP N RGD:5509061 20171005 MGI PMID:16890163 1321120 Hoxb1 homeobox B1 gene MP:0030141 facial paralysis IAGP N RGD:5509061 20171005 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0030142 facial muscle degeneration IAGP N RGD:5509061 20171005 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0030146 abnormal digastric posterior belly morphology IAGP N RGD:5509061 20171005 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0030146 abnormal digastric posterior belly morphology IAGP N RGD:5509061 20171005 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0030149 abnormal stylohyoid muscle morphology IAGP N RGD:5509061 20171005 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0030151 abnormal buccinator muscle morphology IAGP N RGD:5509061 20171005 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0030152 abnormal depressor anguli oris muscle morphology IAGP N RGD:5509061 20171005 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0030174 absent orbicularis oculi muscle IAGP N RGD:5509061 20171005 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0030177 absent levator labii superioris muscle IAGP N RGD:5509061 20171005 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0030184 abnormal zygomaticus muscle morphology IAGP N RGD:5509061 20171012 MGI PMID:8898234 1321120 Hoxb1 homeobox B1 gene MP:0030207 absent zygomaticus muscle IAGP N RGD:5509061 20171019 MGI PMID:10529420 1321120 Hoxb1 homeobox B1 gene MP:0030430 absent levator nasolabialis muscle IAGP N RGD:5509061 20171214 MGI PMID:8898234 1321122 Pin1 peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:11805292 1321122 Pin1 peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11805292 1321122 Pin1 peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12810604 1321122 Pin1 peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12810604 1321122 Pin1 peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12810604 1321122 Pin1 peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:16554819 1321122 Pin1 peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11805292 1321122 Pin1 peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:11805292 1321122 Pin1 peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:11805292 1321122 Pin1 peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12810604 1321122 Pin1 peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:12810604 1321122 Pin1 peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1 gene MP:0030934 decreased primordial germ cell proliferation IAGP N RGD:5509061 20190411 MGI PMID:12810604 1321122 Pin1 peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:11805292 1321124 Plekhg1 pleckstrin homology domain containing, family G (with RhoGef domain) member 1 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20160804 MGI 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20802511 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:18268034 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0001147 small testis IAGP N RGD:5509061 20220210 MGI PMID:31373619 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220210 MGI PMID:31373619 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15299027 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15299027 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:15299027 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15299027 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20802511 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15299027 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20220210 MGI PMID:31373619 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18268034 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220210 MGI PMID:31373619 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220210 MGI PMID:31373619 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220210 MGI PMID:31373619 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:20802511 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20802511 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:20802511 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:18268034 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220210 MGI PMID:31373619 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:15299027 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18268034 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220210 MGI PMID:31373619 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220210 MGI PMID:31373619 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18268034 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:20802511 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18268034 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220210 MGI PMID:31373619 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0010039 abnormal trophoblast giant cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15299027 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20802511 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15299027 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20802511 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220210 MGI PMID:31373619 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:20802511 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:15299027 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:20802511 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0013589 thymus medulla hypoplasia IAGP N RGD:5509061 20150319 MGI PMID:18268034 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220210 MGI PMID:31373619 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220210 MGI PMID:31373619 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220303 MGI PMID:31373619 1321126 Cops5 COP9 signalosome subunit 5 gene MP:0031389 abnormal ectoplasmic specialization morphology IAGP N RGD:5509061 20220428 MGI PMID:31373619 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15936750 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15936750 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15936750 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:14993236 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:14993236 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11839819 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15936750 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20151203 MGI PMID:20376065 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0002748 abnormal pulmonary valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20151203 MGI PMID:19273593 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20151203 MGI PMID:19409519 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20151203 MGI PMID:19409519 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20151203 MGI PMID:19409519 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20151203 MGI PMID:19273593 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15936750 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0010618 enlarged mitral valve IAGP N RGD:5509061 20141003 MGI PMID:15936750 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0010620 thick mitral valve IAGP N RGD:5509061 20141003 MGI PMID:15936750 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0010620 thick mitral valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0010629 thick tricuspid valve IAGP N RGD:5509061 20141003 MGI PMID:15936750 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0010629 thick tricuspid valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15936750 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20151203 MGI PMID:19409519 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20151203 MGI PMID:19409519 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0012193 increased keratinocyte migration IAGP N RGD:5509061 20151203 MGI PMID:20376065 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0031558 tricuspid valve hyperplasia IAGP N RGD:5509061 20240104 MGI PMID:15936750 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0031581 semilunar valve hyperplasia IAGP N RGD:5509061 20240125 MGI PMID:15936750 1321128 Adam9 ADAM metallopeptidase domain 9 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:19409519 1321131 Fam120b family with sequence similarity 120, member B gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1321131 Fam120b family with sequence similarity 120, member B gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20220217 MGI PMID:34339838 1321131 Fam120b family with sequence similarity 120, member B gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20220217 MGI PMID:34339838 1321131 Fam120b family with sequence similarity 120, member B gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20220217 MGI PMID:34339838 1321131 Fam120b family with sequence similarity 120, member B gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20220217 MGI PMID:34339838 1321131 Fam120b family with sequence similarity 120, member B gene MP:0010580 decreased heart left ventricle size IAGP N RGD:5509061 20220217 MGI PMID:34339838 1321131 Fam120b family with sequence similarity 120, member B gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20220217 MGI PMID:34339838 1321131 Fam120b family with sequence similarity 120, member B gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20220217 MGI PMID:34339838 1321131 Fam120b family with sequence similarity 120, member B gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20220217 MGI PMID:34339838 1321131 Fam120b family with sequence similarity 120, member B gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20220217 MGI PMID:34339838 1321131 Fam120b family with sequence similarity 120, member B gene MP:0031609 increased fetal cardiomyocyte size IAGP N RGD:5509061 20240321 MGI PMID:34339838 1321133 Ubash3a ubiquitin associated and SH3 domain containing, A gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1321133 Ubash3a ubiquitin associated and SH3 domain containing, A gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1321133 Ubash3a ubiquitin associated and SH3 domain containing, A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14738763 1321133 Ubash3a ubiquitin associated and SH3 domain containing, A gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20201022 MGI 1321133 Ubash3a ubiquitin associated and SH3 domain containing, A gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:14738763 1321133 Ubash3a ubiquitin associated and SH3 domain containing, A gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:14738763 1321133 Ubash3a ubiquitin associated and SH3 domain containing, A gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14738763 1321133 Ubash3a ubiquitin associated and SH3 domain containing, A gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:14738763 1321133 Ubash3a ubiquitin associated and SH3 domain containing, A gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:14738763 1321133 Ubash3a ubiquitin associated and SH3 domain containing, A gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1321133 Ubash3a ubiquitin associated and SH3 domain containing, A gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1321135 Mtmr4 myotubularin related protein 4 gene MP:0002492 decreased IgE level IEA N RGD:5509061 20160804 MGI 1321138 Ptcd2 pentatricopeptide repeat domain 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18729827 1321138 Ptcd2 pentatricopeptide repeat domain 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18729827 1321138 Ptcd2 pentatricopeptide repeat domain 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18729827 1321138 Ptcd2 pentatricopeptide repeat domain 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:18729827 1321138 Ptcd2 pentatricopeptide repeat domain 2 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18729827 1321138 Ptcd2 pentatricopeptide repeat domain 2 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:18729827 1321138 Ptcd2 pentatricopeptide repeat domain 2 gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:18729827 1321138 Ptcd2 pentatricopeptide repeat domain 2 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:18729827 1321138 Ptcd2 pentatricopeptide repeat domain 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18729827 1321138 Ptcd2 pentatricopeptide repeat domain 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:18729827 1321138 Ptcd2 pentatricopeptide repeat domain 2 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:18729827 1321140 Qprt quinolinate phosphoribosyltransferase gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20210819 MGI PMID:30478397 1321140 Qprt quinolinate phosphoribosyltransferase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20210819 MGI PMID:30478397 1321140 Qprt quinolinate phosphoribosyltransferase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20210819 MGI PMID:30478397 1321140 Qprt quinolinate phosphoribosyltransferase gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20210819 MGI PMID:30478397 1321140 Qprt quinolinate phosphoribosyltransferase gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20210819 MGI PMID:30478397 1321141 Kif7 kinesin family member 7 gene MP:0000111 cleft palate IEA N RGD:5509061 20141003 MGI 1321141 Kif7 kinesin family member 7 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:19549984 1321141 Kif7 kinesin family member 7 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:19549984 1321141 Kif7 kinesin family member 7 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:19549984 1321141 Kif7 kinesin family member 7 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:19549984 1321141 Kif7 kinesin family member 7 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20141003 MGI 1321141 Kif7 kinesin family member 7 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1321141 Kif7 kinesin family member 7 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19549984 1321141 Kif7 kinesin family member 7 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19592253 1321141 Kif7 kinesin family member 7 gene MP:0000564 syndactyly IEA N RGD:5509061 20141003 MGI 1321141 Kif7 kinesin family member 7 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19549984 1321141 Kif7 kinesin family member 7 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19592253 1321141 Kif7 kinesin family member 7 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:19666503 1321141 Kif7 kinesin family member 7 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19666503 1321141 Kif7 kinesin family member 7 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:19592253 1321141 Kif7 kinesin family member 7 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23650387 1321141 Kif7 kinesin family member 7 gene MP:0001293 anophthalmia IEA N RGD:5509061 20141003 MGI 1321141 Kif7 kinesin family member 7 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19592253 1321141 Kif7 kinesin family member 7 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19549984 1321141 Kif7 kinesin family member 7 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19592253 1321141 Kif7 kinesin family member 7 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20141003 MGI 1321141 Kif7 kinesin family member 7 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19549984 1321141 Kif7 kinesin family member 7 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19666503 1321141 Kif7 kinesin family member 7 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23650387 1321141 Kif7 kinesin family member 7 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:23650387 1321141 Kif7 kinesin family member 7 gene MP:0003936 abnormal reproductive system development IEA N RGD:5509061 20141003 MGI 1321141 Kif7 kinesin family member 7 gene MP:0004157 interrupted aortic arch IEA N RGD:5509061 20141003 MGI 1321141 Kif7 kinesin family member 7 gene MP:0004949 absent neuronal precursor cells IAGP N RGD:5509061 20141003 MGI PMID:19549984 1321141 Kif7 kinesin family member 7 gene MP:0005170 cleft upper lip IEA N RGD:5509061 20141003 MGI 1321141 Kif7 kinesin family member 7 gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19666503 1321141 Kif7 kinesin family member 7 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:23650387 1321141 Kif7 kinesin family member 7 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:19592253 1321141 Kif7 kinesin family member 7 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:23650387 1321141 Kif7 kinesin family member 7 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19549984 1321141 Kif7 kinesin family member 7 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19592253 1321141 Kif7 kinesin family member 7 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19666503 1321141 Kif7 kinesin family member 7 gene MP:0009744 postaxial polydactyly IEA N RGD:5509061 20141003 MGI 1321141 Kif7 kinesin family member 7 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19549984 1321141 Kif7 kinesin family member 7 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23650387 1321141 Kif7 kinesin family member 7 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1321141 Kif7 kinesin family member 7 gene MP:0010460 pulmonary artery hypoplasia IEA N RGD:5509061 20141003 MGI 1321141 Kif7 kinesin family member 7 gene MP:0010975 abnormal lung lobe morphology IEA N RGD:5509061 20141003 MGI 1321141 Kif7 kinesin family member 7 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19549984 1321141 Kif7 kinesin family member 7 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19666503 1321141 Kif7 kinesin family member 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19666503 1321141 Kif7 kinesin family member 7 gene MP:0012059 thick diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:23650387 1321141 Kif7 kinesin family member 7 gene MP:0012060 diaphragm muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23650387 1321141 Kif7 kinesin family member 7 gene MP:0012061 abnormal diaphragm central tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:23650387 1321141 Kif7 kinesin family member 7 gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20141003 MGI PMID:23650387 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20191128 MGI 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191128 MGI 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0002861 abnormal tail bud morphology IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20240523 MGI 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20240523 MGI 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0011249 abdominal situs inversus IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0011252 situs inversus totalis IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20221215 MGI 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0011649 immotile respiratory cilia IAGP N RGD:5509061 20141003 MGI PMID:23525783 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0012277 increased tail bud apoptosis IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0013197 decreased embryonic cilium number IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20191128 MGI PMID:31107948 1321143 Dnaaf2 dynein, axonemal assembly factor 2 gene MP:0030963 abnormal brain ependyma motile cilium location or orientation IAGP N RGD:5509061 20190725 MGI PMID:23525783 1321147 Farsa phenylalanyl-tRNA synthetase, alpha subunit gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20141003 MGI 1321147 Farsa phenylalanyl-tRNA synthetase, alpha subunit gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1321147 Farsa phenylalanyl-tRNA synthetase, alpha subunit gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1321147 Farsa phenylalanyl-tRNA synthetase, alpha subunit gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20150108 MGI 1321147 Farsa phenylalanyl-tRNA synthetase, alpha subunit gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20150430 MGI 1321147 Farsa phenylalanyl-tRNA synthetase, alpha subunit gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20150108 MGI 1321147 Farsa phenylalanyl-tRNA synthetase, alpha subunit gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1321147 Farsa phenylalanyl-tRNA synthetase, alpha subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321148 Prox2 prospero homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16470382 1321148 Prox2 prospero homeobox 2 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20190502 MGI 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0010493 abnormal atrium myocardium morphology IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321150 Pabir1 PP2A A alpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20240905 MGI PMID:36715298 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0000603 pale liver IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321152 Kbtbd2 kelch repeat and BTB (POZ) domain containing 2 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20161124 MGI PMID:27708159 1321154 Cnot4 CCR4-NOT transcription complex, subunit 4 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1321154 Cnot4 CCR4-NOT transcription complex, subunit 4 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1321154 Cnot4 CCR4-NOT transcription complex, subunit 4 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1321154 Cnot4 CCR4-NOT transcription complex, subunit 4 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 1321154 Cnot4 CCR4-NOT transcription complex, subunit 4 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20181227 MGI 1321154 Cnot4 CCR4-NOT transcription complex, subunit 4 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1321154 Cnot4 CCR4-NOT transcription complex, subunit 4 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1321154 Cnot4 CCR4-NOT transcription complex, subunit 4 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1321154 Cnot4 CCR4-NOT transcription complex, subunit 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20210805 MGI PMID:34026442 1321154 Cnot4 CCR4-NOT transcription complex, subunit 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1321154 Cnot4 CCR4-NOT transcription complex, subunit 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321154 Cnot4 CCR4-NOT transcription complex, subunit 4 gene MP:0012768 decreased KLRG1-positive NK cell number IEA N RGD:5509061 20201022 MGI 1321154 Cnot4 CCR4-NOT transcription complex, subunit 4 gene MP:0013406 abnormal epidermal immune compartment IEA N RGD:5509061 20201231 MGI 1321158 Me2 malic enzyme 2, NAD(+)-dependent, mitochondrial gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 1321160 Slc39a5 solute carrier family 39 (metal ion transporter), member 5 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20220519 MGI 1321160 Slc39a5 solute carrier family 39 (metal ion transporter), member 5 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1321160 Slc39a5 solute carrier family 39 (metal ion transporter), member 5 gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20141003 MGI PMID:24303081 1321160 Slc39a5 solute carrier family 39 (metal ion transporter), member 5 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1321160 Slc39a5 solute carrier family 39 (metal ion transporter), member 5 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:24303081 1321160 Slc39a5 solute carrier family 39 (metal ion transporter), member 5 gene MP:0009150 pancreatic acinar cell atrophy IAGP N RGD:5509061 20141003 MGI PMID:24303081 1321160 Slc39a5 solute carrier family 39 (metal ion transporter), member 5 gene MP:0009615 abnormal zinc homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24303081 1321160 Slc39a5 solute carrier family 39 (metal ion transporter), member 5 gene MP:0011924 abnormal liver zinc level IAGP N RGD:5509061 20141003 MGI PMID:24303081 1321161 Frmd8 FERM domain containing 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20181108 MGI PMID:29897336 1321161 Frmd8 FERM domain containing 8 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20231130 MGI PMID:37527040 1321161 Frmd8 FERM domain containing 8 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20231130 MGI PMID:37527040 1321161 Frmd8 FERM domain containing 8 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20231130 MGI PMID:37527040 1321161 Frmd8 FERM domain containing 8 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20231130 MGI PMID:37527040 1321161 Frmd8 FERM domain containing 8 gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20231130 MGI PMID:37527040 1321161 Frmd8 FERM domain containing 8 gene MP:0013955 increased colon length IAGP N RGD:5509061 20231130 MGI PMID:37527040 1321162 Zswim7 zinc finger SWIM-type containing 7 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20190502 MGI PMID:30305635 1321162 Zswim7 zinc finger SWIM-type containing 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20190502 MGI PMID:30305635 1321162 Zswim7 zinc finger SWIM-type containing 7 gene MP:0001926 female infertility IAGP N RGD:5509061 20190502 MGI PMID:30305635 1321162 Zswim7 zinc finger SWIM-type containing 7 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20190502 MGI PMID:30305635 1321162 Zswim7 zinc finger SWIM-type containing 7 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20190502 MGI PMID:30305635 1321162 Zswim7 zinc finger SWIM-type containing 7 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20190502 MGI PMID:30305635 1321162 Zswim7 zinc finger SWIM-type containing 7 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20190502 MGI PMID:30305635 1321162 Zswim7 zinc finger SWIM-type containing 7 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20190502 MGI PMID:30305635 1321162 Zswim7 zinc finger SWIM-type containing 7 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20190502 MGI PMID:30305635 1321162 Zswim7 zinc finger SWIM-type containing 7 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20190502 MGI PMID:30305635 1321162 Zswim7 zinc finger SWIM-type containing 7 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20190502 MGI PMID:30305635 1321162 Zswim7 zinc finger SWIM-type containing 7 gene MP:0013507 increased ovary apoptosis IAGP N RGD:5509061 20190502 MGI PMID:30305635 1321164 Chchd3 coiled-coil-helix-coiled-coil-helix domain containing 3 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20111116 MGI 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210826 MGI 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0001925 male infertility IAGP N RGD:5509061 20240801 MGI PMID:38597936 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240801 MGI PMID:38597936 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20210826 MGI 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0003960 increased lean body mass IEA N RGD:5509061 20240523 MGI 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0005102 abnormal iris pigmentation IEA N RGD:5509061 20201022 MGI 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220811 MGI 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20240801 MGI PMID:38597936 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240801 MGI PMID:38597936 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0009231 detached acrosome IAGP N RGD:5509061 20240801 MGI PMID:38597936 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0009235 small sperm head IAGP N RGD:5509061 20240801 MGI PMID:38597936 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210826 MGI 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20240801 MGI PMID:38597936 1321165 Ccdc28a coiled-coil domain containing 28A gene MP:0030980 abnormal acroplaxome morphology IAGP N RGD:5509061 20240801 MGI PMID:38597936 1321167 Stab1 stabilin 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:21293057 1321167 Stab1 stabilin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21293057 1321167 Stab1 stabilin 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:21293057 1321167 Stab1 stabilin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21293057 1321167 Stab1 stabilin 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:21293057 1321167 Stab1 stabilin 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:21293057 1321167 Stab1 stabilin 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21293057 1321167 Stab1 stabilin 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:21293057 1321167 Stab1 stabilin 1 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:21293057 1321167 Stab1 stabilin 1 gene MP:0011009 increased circulating glutamate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:21293057 1321167 Stab1 stabilin 1 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21293057 1321167 Stab1 stabilin 1 gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21293057 1321169 Pcdhb22 protocadherin beta 22 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1321169 Pcdhb22 protocadherin beta 22 gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1321169 Pcdhb22 protocadherin beta 22 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1321174 Bloc1s3 biogenesis of lysosomal organelles complex-1, subunit 3 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:7203014 1321174 Bloc1s3 biogenesis of lysosomal organelles complex-1, subunit 3 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7203014 1321174 Bloc1s3 biogenesis of lysosomal organelles complex-1, subunit 3 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:7089489 1321174 Bloc1s3 biogenesis of lysosomal organelles complex-1, subunit 3 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:7203014 1321174 Bloc1s3 biogenesis of lysosomal organelles complex-1, subunit 3 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:12445206 1321174 Bloc1s3 biogenesis of lysosomal organelles complex-1, subunit 3 gene MP:0008731 abnormal hair shaft melanin granule morphology IAGP N RGD:5509061 20181129 MGI PMID:7203014 1321174 Bloc1s3 biogenesis of lysosomal organelles complex-1, subunit 3 gene MP:0009779 enhanced behavioral response to anesthetic IAGP N RGD:5509061 20141003 MGI PMID:2513223 1321174 Bloc1s3 biogenesis of lysosomal organelles complex-1, subunit 3 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7089489 1321174 Bloc1s3 biogenesis of lysosomal organelles complex-1, subunit 3 gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7203014 1321174 Bloc1s3 biogenesis of lysosomal organelles complex-1, subunit 3 gene MP:0011279 decreased ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7203014 1321176 Cyfip1 cytoplasmic FMR1 interacting protein 1 gene MP:0000929 open neural tube IEA N RGD:5509061 20111116 MGI 1321176 Cyfip1 cytoplasmic FMR1 interacting protein 1 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20160324 MGI PMID:26474913 1321176 Cyfip1 cytoplasmic FMR1 interacting protein 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160324 MGI PMID:26474913 1321176 Cyfip1 cytoplasmic FMR1 interacting protein 1 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20160324 MGI PMID:26474913 1321176 Cyfip1 cytoplasmic FMR1 interacting protein 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20160324 MGI PMID:26474913 1321176 Cyfip1 cytoplasmic FMR1 interacting protein 1 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20160324 MGI PMID:26474913 1321176 Cyfip1 cytoplasmic FMR1 interacting protein 1 gene MP:0003400 kinked neural tube IEA N RGD:5509061 20111116 MGI 1321176 Cyfip1 cytoplasmic FMR1 interacting protein 1 gene MP:0003794 delayed somite formation IEA N RGD:5509061 20111116 MGI 1321176 Cyfip1 cytoplasmic FMR1 interacting protein 1 gene MP:0003885 abnormal rostral-caudal body axis extension IEA N RGD:5509061 20111116 MGI 1321176 Cyfip1 cytoplasmic FMR1 interacting protein 1 gene MP:0009455 enhanced cued conditioning behavior IAGP N RGD:5509061 20160324 MGI PMID:26474913 1321176 Cyfip1 cytoplasmic FMR1 interacting protein 1 gene MP:0009768 impaired somite development IEA N RGD:5509061 20111116 MGI 1321176 Cyfip1 cytoplasmic FMR1 interacting protein 1 gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1321176 Cyfip1 cytoplasmic FMR1 interacting protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160324 MGI PMID:26474913 1321176 Cyfip1 cytoplasmic FMR1 interacting protein 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IEA N RGD:5509061 20141003 MGI 1321178 Itga3 integrin alpha 3 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:19118220 1321178 Itga3 integrin alpha 3 gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:19104148 1321178 Itga3 integrin alpha 3 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:19118220 1321178 Itga3 integrin alpha 3 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:19118220 1321178 Itga3 integrin alpha 3 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12904471 1321178 Itga3 integrin alpha 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12904471 1321178 Itga3 integrin alpha 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17848500 1321178 Itga3 integrin alpha 3 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17015618 1321178 Itga3 integrin alpha 3 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19104148 1321178 Itga3 integrin alpha 3 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:19118220 1321178 Itga3 integrin alpha 3 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:17015618 1321178 Itga3 integrin alpha 3 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:17015618 1321178 Itga3 integrin alpha 3 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23792458 1321178 Itga3 integrin alpha 3 gene MP:0003591 urethra atresia IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0003826 abnormal Mullerian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0004202 pulmonary hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19104148 1321178 Itga3 integrin alpha 3 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23792458 1321178 Itga3 integrin alpha 3 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0004757 abnormal distal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:19118220 1321178 Itga3 integrin alpha 3 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:17015618 1321178 Itga3 integrin alpha 3 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17015618 1321178 Itga3 integrin alpha 3 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19104148 1321178 Itga3 integrin alpha 3 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0008138 absent podocyte foot process IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:17015618 1321178 Itga3 integrin alpha 3 gene MP:0008509 disorganized retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:17015618 1321178 Itga3 integrin alpha 3 gene MP:0009111 pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0009252 absent urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0009569 abnormal left lung morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0009570 abnormal right lung morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23792458 1321178 Itga3 integrin alpha 3 gene MP:0010116 abnormal primitive urogenital sinus morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:19104148 1321178 Itga3 integrin alpha 3 gene MP:0010896 decreased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:19104148 1321178 Itga3 integrin alpha 3 gene MP:0010897 abnormal bronchiole epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0011011 impaired lung lobe morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0011032 impaired branching involved in terminal bronchiole morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10433923 1321178 Itga3 integrin alpha 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1321178 Itga3 integrin alpha 3 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17015618 1321178 Itga3 integrin alpha 3 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0011359 decreased glomerular capillary number IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:17015618 1321178 Itga3 integrin alpha 3 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:17015618 1321178 Itga3 integrin alpha 3 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0011509 dilated glomerular capillary IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0011846 decreased kidney collecting duct number IAGP N RGD:5509061 20141003 MGI PMID:8951069 1321178 Itga3 integrin alpha 3 gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:17848500 1321182 Ccl19 C-C motif chemokine ligand 19 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:17893676 1321182 Ccl19 C-C motif chemokine ligand 19 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17893676 1321186 Psca prostate stem cell antigen gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20170105 MGI 1321186 Psca prostate stem cell antigen gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18044730 1321186 Psca prostate stem cell antigen gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:18044730 1321186 Psca prostate stem cell antigen gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18044730 1321186 Psca prostate stem cell antigen gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18044730 1321186 Psca prostate stem cell antigen gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1321191 Shprh SNF2 histone linker PHD RING helicase gene MP:0000709 enlarged thymus IEA N RGD:5509061 20181227 MGI 1321191 Shprh SNF2 histone linker PHD RING helicase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1321191 Shprh SNF2 histone linker PHD RING helicase gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 1321193 Dclre1b DNA cross-link repair 1B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20551906 1321193 Dclre1b DNA cross-link repair 1B gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20551906 1321195 Mesd mesoderm development LRP chaperone gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:24124512 1321195 Mesd mesoderm development LRP chaperone gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20150305 MGI PMID:21337463 1321195 Mesd mesoderm development LRP chaperone gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20150305 MGI PMID:21337463 1321195 Mesd mesoderm development LRP chaperone gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:24124512 1321195 Mesd mesoderm development LRP chaperone gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20150305 MGI PMID:21337463 1321195 Mesd mesoderm development LRP chaperone gene MP:0011187 abnormal parietal endoderm morphology IAGP N RGD:5509061 20150305 MGI PMID:21337463 1321195 Mesd mesoderm development LRP chaperone gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:24124512 1321195 Mesd mesoderm development LRP chaperone gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20150305 MGI PMID:21337463 1321197 Dhx38 DEAH-box helicase 38 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1321197 Dhx38 DEAH-box helicase 38 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1321197 Dhx38 DEAH-box helicase 38 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1321197 Dhx38 DEAH-box helicase 38 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1321197 Dhx38 DEAH-box helicase 38 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321197 Dhx38 DEAH-box helicase 38 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1321201 Tango2 transport and golgi organization 2 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20230601 MGI 1321201 Tango2 transport and golgi organization 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1321202 Oas1c 2'-5' oligoadenylate synthetase 1C gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20221215 MGI 1321202 Oas1c 2'-5' oligoadenylate synthetase 1C gene MP:0000692 small spleen IEA N RGD:5509061 20221215 MGI 1321202 Oas1c 2'-5' oligoadenylate synthetase 1C gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20221215 MGI 1321202 Oas1c 2'-5' oligoadenylate synthetase 1C gene MP:0000709 enlarged thymus IEA N RGD:5509061 20221215 MGI 1321202 Oas1c 2'-5' oligoadenylate synthetase 1C gene MP:0001293 anophthalmia IEA N RGD:5509061 20221215 MGI 1321202 Oas1c 2'-5' oligoadenylate synthetase 1C gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20221215 MGI 1321202 Oas1c 2'-5' oligoadenylate synthetase 1C gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20221215 MGI 1321204 Cdx1 caudal type homeobox 1 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14660544 1321204 Cdx1 caudal type homeobox 1 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7585967 1321204 Cdx1 caudal type homeobox 1 gene MP:0000080 abnormal exoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7585967 1321204 Cdx1 caudal type homeobox 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:14660544 1321204 Cdx1 caudal type homeobox 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:17537796 1321204 Cdx1 caudal type homeobox 1 gene MP:0000151 absent ribs IAGP N RGD:5509061 20141003 MGI PMID:14660544 1321204 Cdx1 caudal type homeobox 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:14660544 1321204 Cdx1 caudal type homeobox 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:7585967 1321204 Cdx1 caudal type homeobox 1 gene MP:0000373 belly spot IAGP N RGD:5509061 20160616 MGI PMID:26952979 1321204 Cdx1 caudal type homeobox 1 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22190642 1321204 Cdx1 caudal type homeobox 1 gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20160616 MGI PMID:26952979 1321204 Cdx1 caudal type homeobox 1 gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20160616 MGI PMID:26952979 1321204 Cdx1 caudal type homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19328777 1321204 Cdx1 caudal type homeobox 1 gene MP:0002938 white spotting IAGP N RGD:5509061 20160616 MGI PMID:26952979 1321204 Cdx1 caudal type homeobox 1 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7585967 1321204 Cdx1 caudal type homeobox 1 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:16396910 1321204 Cdx1 caudal type homeobox 1 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:18511567 1321204 Cdx1 caudal type homeobox 1 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:14660544 1321204 Cdx1 caudal type homeobox 1 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:17537796 1321204 Cdx1 caudal type homeobox 1 gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20141003 MGI PMID:14660544 1321204 Cdx1 caudal type homeobox 1 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:17537796 1321204 Cdx1 caudal type homeobox 1 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:14660544 1321204 Cdx1 caudal type homeobox 1 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:14660544 1321204 Cdx1 caudal type homeobox 1 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17537796 1321204 Cdx1 caudal type homeobox 1 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16396910 1321204 Cdx1 caudal type homeobox 1 gene MP:0004658 abnormal ventral tubercle of atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:14660544 1321204 Cdx1 caudal type homeobox 1 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17537796 1321204 Cdx1 caudal type homeobox 1 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7585967 1321204 Cdx1 caudal type homeobox 1 gene MP:0009784 abnormal melanoblast migration IAGP N RGD:5509061 20160616 MGI PMID:26952979 1321204 Cdx1 caudal type homeobox 1 gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20141003 MGI PMID:14660544 1321204 Cdx1 caudal type homeobox 1 gene MP:0030282 broad supraoccipital bone IAGP N RGD:5509061 20171102 MGI PMID:7585967 1321205 Efcab14 EF-hand calcium binding domain 14 gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20211021 MGI 1321205 Efcab14 EF-hand calcium binding domain 14 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1321205 Efcab14 EF-hand calcium binding domain 14 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1321205 Efcab14 EF-hand calcium binding domain 14 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210128 MGI 1321205 Efcab14 EF-hand calcium binding domain 14 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1321205 Efcab14 EF-hand calcium binding domain 14 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12024045 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0000597 delayed hepatic development IAGP N RGD:5509061 20141003 MGI PMID:12024045 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12024045 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:21954064 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12024045 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12024045 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:12024045 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12417726 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12417726 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:12417726 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21954064 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:21954064 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21954064 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21954064 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:12024045 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12024045 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20230615 MGI PMID:12024045 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0014010 abnormal peroxisome morphology IAGP N RGD:5509061 20230615 MGI PMID:12024045 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0014010 abnormal peroxisome morphology IAGP N RGD:5509061 20230615 MGI PMID:12417726 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0020847 abnormal peroxisome physiology IAGP N RGD:5509061 20230615 MGI PMID:12024045 1321209 Pex11b peroxisomal biogenesis factor 11 beta gene MP:0020847 abnormal peroxisome physiology IAGP N RGD:5509061 20230615 MGI PMID:12417726 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20161020 MGI PMID:26431380 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20161020 MGI PMID:26431380 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20161020 MGI PMID:26431380 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20161020 MGI PMID:26431380 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161020 MGI PMID:26431380 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22542455 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20240229 MGI PMID:30718289 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20161020 MGI PMID:26431380 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22542455 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0005039 hypoxia IAGP N RGD:5509061 20240229 MGI PMID:30718289 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20161020 MGI PMID:26431380 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20161020 MGI PMID:26431380 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20240229 MGI PMID:30718289 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0010802 abnormal intestinal enteroendocrine cell morphology IAGP N RGD:5509061 20161020 MGI PMID:26431380 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20240229 MGI PMID:30718289 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20240229 MGI PMID:30718289 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22542455 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20240229 MGI PMID:30718289 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240229 MGI PMID:30718289 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0011525 abnormal placenta intervillous maternal lacunae morphology IAGP N RGD:5509061 20240229 MGI PMID:30718289 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20161020 MGI PMID:26431380 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0013485 increased Paneth cell number IAGP N RGD:5509061 20161020 MGI PMID:26431380 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:22542455 1321211 Usp22 ubiquitin specific peptidase 22 gene MP:0013794 abnormal intestinal villus goblet cell morphology IAGP N RGD:5509061 20161020 MGI PMID:26431380 1321218 Uri1 URI1, prefoldin-like chaperone gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20191205 MGI PMID:25453901 1321218 Uri1 URI1, prefoldin-like chaperone gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20191205 MGI PMID:25453901 1321218 Uri1 URI1, prefoldin-like chaperone gene MP:0001860 liver inflammation IAGP N RGD:5509061 20191205 MGI PMID:25453901 1321218 Uri1 URI1, prefoldin-like chaperone gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20191205 MGI PMID:25453901 1321218 Uri1 URI1, prefoldin-like chaperone gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20191205 MGI PMID:25453901 1321218 Uri1 URI1, prefoldin-like chaperone gene MP:0003326 liver failure IAGP N RGD:5509061 20191205 MGI PMID:25453901 1321218 Uri1 URI1, prefoldin-like chaperone gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20191205 MGI PMID:25453901 1321218 Uri1 URI1, prefoldin-like chaperone gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20191205 MGI PMID:25453901 1321218 Uri1 URI1, prefoldin-like chaperone gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20191205 MGI PMID:25453901 1321218 Uri1 URI1, prefoldin-like chaperone gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20191205 MGI PMID:25453901 1321218 Uri1 URI1, prefoldin-like chaperone gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20191205 MGI PMID:25453901 1321218 Uri1 URI1, prefoldin-like chaperone gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210520 MGI 1321220 Ldb1 LIM domain binding 1 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20221201 MGI PMID:24433583 1321220 Ldb1 LIM domain binding 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:23390196 1321220 Ldb1 LIM domain binding 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:15857913 1321220 Ldb1 LIM domain binding 1 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17664423 1321220 Ldb1 LIM domain binding 1 gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:17664423 1321220 Ldb1 LIM domain binding 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:17664423 1321220 Ldb1 LIM domain binding 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:23390196 1321220 Ldb1 LIM domain binding 1 gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17316599 1321220 Ldb1 LIM domain binding 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15857913 1321220 Ldb1 LIM domain binding 1 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:17316599 1321220 Ldb1 LIM domain binding 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:17316599 1321220 Ldb1 LIM domain binding 1 gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15857913 1321220 Ldb1 LIM domain binding 1 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:23390196 1321220 Ldb1 LIM domain binding 1 gene MP:0004713 split notochord IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0006400 decreased molar number IAGP N RGD:5509061 20221201 MGI PMID:24433583 1321220 Ldb1 LIM domain binding 1 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:17316599 1321220 Ldb1 LIM domain binding 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:17316599 1321220 Ldb1 LIM domain binding 1 gene MP:0008391 abnormal primordial germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20221201 MGI PMID:24433583 1321220 Ldb1 LIM domain binding 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221201 MGI PMID:24433583 1321220 Ldb1 LIM domain binding 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221201 MGI PMID:24433583 1321220 Ldb1 LIM domain binding 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17316599 1321220 Ldb1 LIM domain binding 1 gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20141003 MGI PMID:17316599 1321220 Ldb1 LIM domain binding 1 gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:17316599 1321220 Ldb1 LIM domain binding 1 gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17316599 1321220 Ldb1 LIM domain binding 1 gene MP:0011455 absent glomerular endothelium fenestra IAGP N RGD:5509061 20141003 MGI PMID:17316599 1321220 Ldb1 LIM domain binding 1 gene MP:0011483 renal glomerular synechia IAGP N RGD:5509061 20141003 MGI PMID:17316599 1321220 Ldb1 LIM domain binding 1 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0012156 rostral-caudal axis duplication IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0012181 increased somite number IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0012792 abnormal rhombomere 3 morphology IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0012800 abnormal rhombomere 5 morphology IAGP N RGD:5509061 20141003 MGI PMID:12490556 1321220 Ldb1 LIM domain binding 1 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:24433583 1321220 Ldb1 LIM domain binding 1 gene MP:0030536 abnormal diastema morphology IAGP N RGD:5509061 20221201 MGI PMID:24433583 1321220 Ldb1 LIM domain binding 1 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221201 MGI PMID:24433583 1321220 Ldb1 LIM domain binding 1 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:24433583 1321220 Ldb1 LIM domain binding 1 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20221201 MGI PMID:24433583 1321221 Kif18b kinesin family member 18B gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1321221 Kif18b kinesin family member 18B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0000135 decreased compact bone thickness IEA N RGD:5509061 20150917 MGI 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0001406 abnormal gait IEA N RGD:5509061 20150917 MGI 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0005451 abnormal body composition IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321223 Samd4 sterile alpha motif domain containing 4 gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:24799716 1321230 Sel1l3 sel-1 suppressor of lin-12-like 3 (C. elegans) gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 1321230 Sel1l3 sel-1 suppressor of lin-12-like 3 (C. elegans) gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1321230 Sel1l3 sel-1 suppressor of lin-12-like 3 (C. elegans) gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1321232 Snx18 sorting nexin 18 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 1321232 Snx18 sorting nexin 18 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:16700072 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18257070 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:18257070 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:18257070 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17133501 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16700072 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:18257070 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:18257070 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18257070 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:18257070 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:18257070 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17133501 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18257070 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:18257070 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:18257070 1321236 Sfrp5 secreted frizzled-related sequence protein 5 gene MP:0030324 abnormal anterior head development IAGP N RGD:5509061 20180118 MGI PMID:17133501 1321238 Tlk1 tousled-like kinase 1 gene MP:0000745 tremors IAGP N RGD:5509061 20190207 MGI PMID:28708136 1321238 Tlk1 tousled-like kinase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190207 MGI PMID:28708136 1321238 Tlk1 tousled-like kinase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190207 MGI PMID:28708136 1321238 Tlk1 tousled-like kinase 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1321238 Tlk1 tousled-like kinase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20190207 MGI PMID:28708136 1321238 Tlk1 tousled-like kinase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190207 MGI PMID:28708136 1321238 Tlk1 tousled-like kinase 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1321238 Tlk1 tousled-like kinase 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20230601 MGI 1321238 Tlk1 tousled-like kinase 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20240523 MGI 1321238 Tlk1 tousled-like kinase 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1321238 Tlk1 tousled-like kinase 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1321240 Cfap161 cilia and flagella associated protein 161 gene MP:0000452 abnormal mouth morphology IEA N RGD:5509061 20230119 MGI 1321240 Cfap161 cilia and flagella associated protein 161 gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20230119 MGI 1321240 Cfap161 cilia and flagella associated protein 161 gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20230119 MGI 1321240 Cfap161 cilia and flagella associated protein 161 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1321240 Cfap161 cilia and flagella associated protein 161 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1321240 Cfap161 cilia and flagella associated protein 161 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20211104 MGI PMID:34172766 1321240 Cfap161 cilia and flagella associated protein 161 gene MP:0005355 enlarged thyroid gland IEA N RGD:5509061 20230119 MGI 1321240 Cfap161 cilia and flagella associated protein 161 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230119 MGI 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16321985 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:16321985 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16769894 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:16321985 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:16321985 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:16321985 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16107644 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16107644 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16769894 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16107644 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17855450 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18558633 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:16107644 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17855450 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:17855450 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:16107644 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:17855450 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:18558633 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16769894 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16321985 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:16321985 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:18558633 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0004262 abnormal physical strength IAGP N RGD:5509061 20141003 MGI PMID:18558633 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:18558633 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:16321985 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:18558633 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:18558633 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:16321985 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16107644 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:16321985 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:16321985 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:16321985 1321242 Als2 alsin Rho guanine nucleotide exchange factor gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16107644 1321244 Tuft1 tuftelin 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160114 MGI 1321244 Tuft1 tuftelin 1 gene MP:0000410 waved hair IAGP N RGD:5509061 20231019 MGI PMID:37716648 1321244 Tuft1 tuftelin 1 gene MP:0001208 blistering IAGP N RGD:5509061 20231019 MGI PMID:37716648 1321244 Tuft1 tuftelin 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20231019 MGI PMID:37716648 1321244 Tuft1 tuftelin 1 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20231019 MGI PMID:37716648 1321244 Tuft1 tuftelin 1 gene MP:0001340 abnormal eyelid morphology IEA N RGD:5509061 20160211 MGI 1321244 Tuft1 tuftelin 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201022 MGI 1321244 Tuft1 tuftelin 1 gene MP:0001874 acanthosis IAGP N RGD:5509061 20231019 MGI PMID:37716648 1321244 Tuft1 tuftelin 1 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20170105 MGI 1321244 Tuft1 tuftelin 1 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20231019 MGI PMID:37716648 1321244 Tuft1 tuftelin 1 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20231019 MGI PMID:37716648 1321244 Tuft1 tuftelin 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1321244 Tuft1 tuftelin 1 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20231019 MGI PMID:37716648 1321244 Tuft1 tuftelin 1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20231019 MGI PMID:37716648 1321244 Tuft1 tuftelin 1 gene MP:0004241 acantholysis IAGP N RGD:5509061 20231019 MGI PMID:37716648 1321244 Tuft1 tuftelin 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20160211 MGI 1321244 Tuft1 tuftelin 1 gene MP:0010072 increased pruritus IAGP N RGD:5509061 20231019 MGI PMID:37716648 1321244 Tuft1 tuftelin 1 gene MP:0013027 wounding IAGP N RGD:5509061 20231019 MGI PMID:37716648 1321244 Tuft1 tuftelin 1 gene MP:0030578 decreased keratinocyte adhesion IAGP N RGD:5509061 20231019 MGI PMID:37716648 1321246 Fbxo9 f-box protein 9 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1321246 Fbxo9 f-box protein 9 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1321246 Fbxo9 f-box protein 9 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1321246 Fbxo9 f-box protein 9 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20160811 MGI 1321246 Fbxo9 f-box protein 9 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20240523 MGI 1321246 Fbxo9 f-box protein 9 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20160421 MGI 1321246 Fbxo9 f-box protein 9 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1321253 Catsper1 cation channel, sperm associated 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:11595941 1321253 Catsper1 cation channel, sperm associated 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11595941 1321253 Catsper1 cation channel, sperm associated 1 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:17227845 1321253 Catsper1 cation channel, sperm associated 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11595941 1321253 Catsper1 cation channel, sperm associated 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17227845 1321253 Catsper1 cation channel, sperm associated 1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11595941 1321253 Catsper1 cation channel, sperm associated 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:17227845 1321253 Catsper1 cation channel, sperm associated 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20170518 MGI PMID:25675513 1321253 Catsper1 cation channel, sperm associated 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20191226 MGI PMID:11595941 1321253 Catsper1 cation channel, sperm associated 1 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:11595941 1321255 Rangap1 RAN GTPase activating protein 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:8314081 1321255 Rangap1 RAN GTPase activating protein 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:8314081 1321255 Rangap1 RAN GTPase activating protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8314081 1321255 Rangap1 RAN GTPase activating protein 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:8314081 1321255 Rangap1 RAN GTPase activating protein 1 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:8314081 1321255 Rangap1 RAN GTPase activating protein 1 gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:8314081 1321255 Rangap1 RAN GTPase activating protein 1 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8314081 1321255 Rangap1 RAN GTPase activating protein 1 gene MP:0011200 abnormal extraembryonic coelom morphology IAGP N RGD:5509061 20141003 MGI PMID:8314081 1321255 Rangap1 RAN GTPase activating protein 1 gene MP:0011207 absent ectoplacental cavity IAGP N RGD:5509061 20141003 MGI PMID:8314081 1321255 Rangap1 RAN GTPase activating protein 1 gene MP:0011208 small proamniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:8314081 1321257 Arsa arylsulfatase A gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9728336 1321257 Arsa arylsulfatase A gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10505624 1321257 Arsa arylsulfatase A gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9728336 1321257 Arsa arylsulfatase A gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9728336 1321257 Arsa arylsulfatase A gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:9728336 1321257 Arsa arylsulfatase A gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:9728336 1321257 Arsa arylsulfatase A gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10505624 1321257 Arsa arylsulfatase A gene MP:0001393 ataxia IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11430883 1321257 Arsa arylsulfatase A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9728336 1321257 Arsa arylsulfatase A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9728336 1321257 Arsa arylsulfatase A gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:10505624 1321257 Arsa arylsulfatase A gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:9728336 1321257 Arsa arylsulfatase A gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11430883 1321257 Arsa arylsulfatase A gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:11430883 1321257 Arsa arylsulfatase A gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:9728336 1321257 Arsa arylsulfatase A gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11430883 1321257 Arsa arylsulfatase A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:9728336 1321257 Arsa arylsulfatase A gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9728336 1321257 Arsa arylsulfatase A gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:11430883 1321257 Arsa arylsulfatase A gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:9728336 1321257 Arsa arylsulfatase A gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:9728336 1321257 Arsa arylsulfatase A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:9728336 1321257 Arsa arylsulfatase A gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:10505624 1321257 Arsa arylsulfatase A gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0009853 decreased Sertoli cell phagocytosis IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:8962139 1321257 Arsa arylsulfatase A gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321257 Arsa arylsulfatase A gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20220203 MGI PMID:21965315 1321259 Cd163 CD163 antigen gene MP:0001861 lung inflammation IAGP N RGD:5509061 20170525 MGI PMID:26376364 1321259 Cd163 CD163 antigen gene MP:0002281 abnormal respiratory mucosa goblet cell morphology IAGP N RGD:5509061 20170525 MGI PMID:26376364 1321259 Cd163 CD163 antigen gene MP:0003060 increased aerobic running capacity IAGP N RGD:5509061 20170126 MGI PMID:26242746 1321259 Cd163 CD163 antigen gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20170126 MGI PMID:26242746 1321259 Cd163 CD163 antigen gene MP:0009410 abnormal skeletal muscle satellite cell proliferation IAGP N RGD:5509061 20170126 MGI PMID:26242746 1321259 Cd163 CD163 antigen gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20170126 MGI PMID:26242746 1321259 Cd163 CD163 antigen gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20170126 MGI PMID:26242746 1321259 Cd163 CD163 antigen gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20170126 MGI PMID:26242746 1321259 Cd163 CD163 antigen gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20170126 MGI PMID:26242746 1321259 Cd163 CD163 antigen gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:26242746 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20240620 MGI PMID:31324765 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20240620 MGI PMID:31324765 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20240620 MGI PMID:31324765 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20190502 MGI 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20240620 MGI PMID:31324765 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20240620 MGI PMID:31324765 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20240620 MGI PMID:31324765 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20240620 MGI PMID:31324765 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20240620 MGI PMID:31324765 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20240620 MGI PMID:31324765 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20240620 MGI PMID:31324765 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240620 MGI PMID:31324765 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240620 MGI PMID:31324765 1321260 Pptc7 PTC7 protein phosphatase homolog gene MP:0020423 abnormal mitochondrial biogenesis IAGP N RGD:5509061 20240620 MGI PMID:31324765 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20160922 MGI PMID:26109204 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20160811 MGI 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20201022 MGI 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160421 MGI 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20160922 MGI PMID:26109204 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20160922 MGI PMID:26109204 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0003405 abnormal platelet shape IAGP N RGD:5509061 20160922 MGI PMID:26109204 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0003950 abnormal plasma membrane morphology IAGP N RGD:5509061 20160922 MGI PMID:26109204 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20160922 MGI PMID:26109204 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20160922 MGI PMID:26109204 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0005635 decreased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20160922 MGI PMID:26109204 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20160922 MGI PMID:26109204 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:20974805 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0014060 abnormal platelet alpha-granule morphology IAGP N RGD:5509061 20160922 MGI PMID:26109204 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0020431 decreased platelet alpha-granule number IAGP N RGD:5509061 20170720 MGI PMID:26109204 1321267 Pik3c2a phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201001 MGI PMID:26109204 1321271 Lgi2 leucine-rich repeat LGI family, member 2 gene MP:0000745 tremors IAGP N RGD:5509061 20230330 MGI PMID:36828548 1321271 Lgi2 leucine-rich repeat LGI family, member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230330 MGI PMID:36828548 1321271 Lgi2 leucine-rich repeat LGI family, member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230330 MGI PMID:36828548 1321271 Lgi2 leucine-rich repeat LGI family, member 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20230330 MGI PMID:36828548 1321271 Lgi2 leucine-rich repeat LGI family, member 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20230330 MGI PMID:36828548 1321273 Bend6 BEN domain containing 6 gene MP:0001513 limb grasping IEA N RGD:5509061 20220811 MGI 1321277 Cavin4 caveolae associated 4 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20150101 MGI PMID:24567387 1321279 Uros uroporphyrinogen III synthase gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0001202 skin photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0001202 skin photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0004147 increased porphyrin level IAGP N RGD:5509061 20141003 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0005654 porphyria IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0009545 abnormal dermis papillary layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0010163 hemolysis IAGP N RGD:5509061 20201001 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20111116 MGI 1321279 Uros uroporphyrinogen III synthase gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0011414 erythruria IAGP N RGD:5509061 20141003 MGI PMID:16314073 1321279 Uros uroporphyrinogen III synthase gene MP:0012664 decreased circulating haptoglobin level IAGP N RGD:5509061 20201001 MGI PMID:16532394 1321279 Uros uroporphyrinogen III synthase gene MP:0030058 erythrodontia IAGP N RGD:5509061 20170921 MGI PMID:16314073 1321282 Ankrd23 ankyrin repeat domain 23 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:17392382 1321282 Ankrd23 ankyrin repeat domain 23 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141225 MGI PMID:24736439 1321282 Ankrd23 ankyrin repeat domain 23 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:17392382 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20150226 MGI PMID:23118208 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:22177923 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20150226 MGI PMID:23118208 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20150226 MGI PMID:23118208 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0004941 abnormal regulatory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22177923 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20150226 MGI PMID:23118208 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:21130004 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22177923 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0008573 increased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:22177923 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:22177923 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:22177923 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0008648 decreased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:22177923 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22177923 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0009786 decreased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22177923 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22177923 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:22177923 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:22177923 1321285 Siglech sialic acid binding Ig-like lectin H gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:22177923 1321288 Hnrnpa2b1 heterogeneous nuclear ribonucleoprotein A2/B1 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20201210 MGI PMID:31320558 1321288 Hnrnpa2b1 heterogeneous nuclear ribonucleoprotein A2/B1 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20201210 MGI PMID:31320558 1321288 Hnrnpa2b1 heterogeneous nuclear ribonucleoprotein A2/B1 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20201210 MGI PMID:31320558 1321288 Hnrnpa2b1 heterogeneous nuclear ribonucleoprotein A2/B1 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20201210 MGI PMID:31320558 1321288 Hnrnpa2b1 heterogeneous nuclear ribonucleoprotein A2/B1 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20201210 MGI PMID:31320558 1321294 Pkhd1l1 polycystic kidney and hepatic disease 1-like 1 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20191219 MGI PMID:31444330 1321294 Pkhd1l1 polycystic kidney and hepatic disease 1-like 1 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20191219 MGI PMID:31444330 1321294 Pkhd1l1 polycystic kidney and hepatic disease 1-like 1 gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20191219 MGI PMID:31444330 1321294 Pkhd1l1 polycystic kidney and hepatic disease 1-like 1 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20191219 MGI PMID:31444330 1321294 Pkhd1l1 polycystic kidney and hepatic disease 1-like 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20191219 MGI PMID:31444330 1321294 Pkhd1l1 polycystic kidney and hepatic disease 1-like 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20191219 MGI PMID:31444330 1321294 Pkhd1l1 polycystic kidney and hepatic disease 1-like 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20191219 MGI PMID:31444330 1321300 Topbp1 topoisomerase (DNA) II binding protein 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21149450 1321300 Topbp1 topoisomerase (DNA) II binding protein 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22266795 1321300 Topbp1 topoisomerase (DNA) II binding protein 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:21149450 1321300 Topbp1 topoisomerase (DNA) II binding protein 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:23950734 1321300 Topbp1 topoisomerase (DNA) II binding protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21149450 1321300 Topbp1 topoisomerase (DNA) II binding protein 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:21149450 1321300 Topbp1 topoisomerase (DNA) II binding protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21149450 1321300 Topbp1 topoisomerase (DNA) II binding protein 1 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21149450 1321300 Topbp1 topoisomerase (DNA) II binding protein 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23950734 1321300 Topbp1 topoisomerase (DNA) II binding protein 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:21149450 1321304 Tti2 TELO2 interacting protein 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1321304 Tti2 TELO2 interacting protein 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1321304 Tti2 TELO2 interacting protein 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1321304 Tti2 TELO2 interacting protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20240523 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210520 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:23026747 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220811 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:23026747 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0002765 short fibula IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:23026747 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:23026747 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0003109 short femur IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:23026747 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:23026747 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:23026747 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0004355 short radius IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20141003 MGI PMID:23026747 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:23026747 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20210520 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0005352 small cranium IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20230601 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20230601 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20220811 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23026747 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:23026747 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23026747 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20151217 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:23026747 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0030081 small upper incisors IAGP N RGD:5509061 20170928 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0030089 short lower incisors IAGP N RGD:5509061 20170928 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0030090 short upper incisors IAGP N RGD:5509061 20170928 MGI PMID:26219237 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0030447 abnormal presphenoid synchondrosis IAGP N RGD:5509061 20180111 MGI PMID:23026747 1321309 Evc2 EvC ciliary complex subunit 2 gene MP:0030610 absent teeth IEA N RGD:5509061 20210520 MGI 1321310 Trmt2a TRM2 tRNA methyltransferase 2A gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1321312 Nipsnap1 nipsnap homolog 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20141003 MGI 1321312 Nipsnap1 nipsnap homolog 1 gene MP:0003177 allodynia IAGP N RGD:5509061 20141003 MGI PMID:22311985 1321312 Nipsnap1 nipsnap homolog 1 gene MP:0003313 abnormal locomotor activation IEA N RGD:5509061 20141003 MGI 1321312 Nipsnap1 nipsnap homolog 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22311985 1321315 Cpeb1 cytoplasmic polyadenylation element binding protein 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11702780 1321315 Cpeb1 cytoplasmic polyadenylation element binding protein 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11702780 1321315 Cpeb1 cytoplasmic polyadenylation element binding protein 1 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:11702780 1321315 Cpeb1 cytoplasmic polyadenylation element binding protein 1 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11702780 1321315 Cpeb1 cytoplasmic polyadenylation element binding protein 1 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:11702780 1321315 Cpeb1 cytoplasmic polyadenylation element binding protein 1 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:15169862 1321315 Cpeb1 cytoplasmic polyadenylation element binding protein 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11702780 1321315 Cpeb1 cytoplasmic polyadenylation element binding protein 1 gene MP:0003578 absent ovary IAGP N RGD:5509061 20141003 MGI PMID:11702780 1321315 Cpeb1 cytoplasmic polyadenylation element binding protein 1 gene MP:0003582 abnormal ovary development IAGP N RGD:5509061 20141003 MGI PMID:11702780 1321315 Cpeb1 cytoplasmic polyadenylation element binding protein 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11702780 1321315 Cpeb1 cytoplasmic polyadenylation element binding protein 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:11702780 1321315 Cpeb1 cytoplasmic polyadenylation element binding protein 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:11702780 1321315 Cpeb1 cytoplasmic polyadenylation element binding protein 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:11702780 1321318 Vstm4 V-set and transmembrane domain containing 4 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 1321318 Vstm4 V-set and transmembrane domain containing 4 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20200402 MGI PMID:31698979 1321318 Vstm4 V-set and transmembrane domain containing 4 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20200402 MGI PMID:31698979 1321318 Vstm4 V-set and transmembrane domain containing 4 gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20200402 MGI PMID:31698979 1321319 Zfp871 zinc finger protein 871 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20230824 MGI PMID:34257081 1321319 Zfp871 zinc finger protein 871 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20230824 MGI PMID:34257081 1321319 Zfp871 zinc finger protein 871 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230824 MGI PMID:34257081 1321319 Zfp871 zinc finger protein 871 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1321319 Zfp871 zinc finger protein 871 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20230824 MGI PMID:34257081 1321319 Zfp871 zinc finger protein 871 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20230824 MGI PMID:34257081 1321319 Zfp871 zinc finger protein 871 gene MP:0002083 premature death IAGP N RGD:5509061 20230824 MGI PMID:34257081 1321319 Zfp871 zinc finger protein 871 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20230824 MGI PMID:34257081 1321319 Zfp871 zinc finger protein 871 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1321319 Zfp871 zinc finger protein 871 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1321319 Zfp871 zinc finger protein 871 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20230824 MGI PMID:34257081 1321319 Zfp871 zinc finger protein 871 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1321319 Zfp871 zinc finger protein 871 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1321319 Zfp871 zinc finger protein 871 gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20230824 MGI PMID:34257081 1321319 Zfp871 zinc finger protein 871 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20230824 MGI PMID:34257081 1321319 Zfp871 zinc finger protein 871 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321319 Zfp871 zinc finger protein 871 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20230824 MGI PMID:34257081 1321319 Zfp871 zinc finger protein 871 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1321331 Setd5 SET domain containing 5 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20201022 MGI 1321331 Setd5 SET domain containing 5 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20141009 MGI 1321331 Setd5 SET domain containing 5 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20170105 MGI 1321331 Setd5 SET domain containing 5 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20141009 MGI 1321331 Setd5 SET domain containing 5 gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0000632 abnormal pineal gland morphology IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0000706 small thymus IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0000819 abnormal olfactory bulb morphology IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1321331 Setd5 SET domain containing 5 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1321331 Setd5 SET domain containing 5 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20170105 MGI 1321331 Setd5 SET domain containing 5 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20141009 MGI 1321331 Setd5 SET domain containing 5 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1321331 Setd5 SET domain containing 5 gene MP:0002861 abnormal tail bud morphology IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0002951 small thyroid gland IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0002989 small kidney IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0004032 abnormal interventricular groove morphology IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0004158 right aortic arch IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0004201 fetal growth retardation IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20170105 MGI 1321331 Setd5 SET domain containing 5 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1321331 Setd5 SET domain containing 5 gene MP:0004937 dilated heart IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0004973 increased regulatory T cell number IEA N RGD:5509061 20201022 MGI 1321331 Setd5 SET domain containing 5 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1321331 Setd5 SET domain containing 5 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0005358 abnormal incisor morphology IEA N RGD:5509061 20201231 MGI 1321331 Setd5 SET domain containing 5 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160114 MGI 1321331 Setd5 SET domain containing 5 gene MP:0006064 abnormal superior vena cava morphology IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20170105 MGI 1321331 Setd5 SET domain containing 5 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0008922 abnormal cervical rib IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20170105 MGI 1321331 Setd5 SET domain containing 5 gene MP:0010200 enlarged lymphatic vessel IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0010403 atrial septal defect IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0010406 common atrium IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0010432 common ventricle IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0010433 double inlet heart left ventricle IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0010436 abnormal coronary sinus morphology IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0010484 bicuspid aortic valve IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0010487 abnormal right subclavian artery morphology IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0010572 persistent right dorsal aorta IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0010595 abnormal aortic valve cusp morphology IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:34050709 1321331 Setd5 SET domain containing 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1321331 Setd5 SET domain containing 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321331 Setd5 SET domain containing 5 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0013809 absent pectinate muscle IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013810 absent brachiocephalic trunk IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013812 enlarged orbital veins IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013813 dilated hepatic portal vein IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013814 abnormal hepatic portal vein connection IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013842 ductus venosus stenosis IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013864 enlarged paraumbilical vein IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013874 abnormal ductus venosus topology IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013878 abnormal ductus venosus valve topology IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013925 abnormal vascular plexus formation IAGP N RGD:5509061 20190321 MGI PMID:27864380 1321331 Setd5 SET domain containing 5 gene MP:0013948 intraembryonal intestine elongation IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013977 symmetric azygos veins IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0014000 anastomosis between internal carotid artery and basilar artery IEA N RGD:5509061 20170504 MGI 1321331 Setd5 SET domain containing 5 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1321333 Neurod4 neurogenic differentiation 4 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11861467 1321333 Neurod4 neurogenic differentiation 4 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0001422 abnormal drinking behavior IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:11861467 1321333 Neurod4 neurogenic differentiation 4 gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11861467 1321333 Neurod4 neurogenic differentiation 4 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11861467 1321333 Neurod4 neurogenic differentiation 4 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0006095 absent amacrine cells IAGP N RGD:5509061 20141003 MGI PMID:11861467 1321333 Neurod4 neurogenic differentiation 4 gene MP:0006096 absent retina bipolar cells IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0006098 absent cerebellar lobules IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0006105 small tectum IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15105417 1321333 Neurod4 neurogenic differentiation 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11032813 1321333 Neurod4 neurogenic differentiation 4 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:15105417 1321335 Dcstamp dendrocyte expressed seven transmembrane protein gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16061724 1321335 Dcstamp dendrocyte expressed seven transmembrane protein gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:16061724 1321335 Dcstamp dendrocyte expressed seven transmembrane protein gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:16061724 1321335 Dcstamp dendrocyte expressed seven transmembrane protein gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16061724 1321335 Dcstamp dendrocyte expressed seven transmembrane protein gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:16061724 1321335 Dcstamp dendrocyte expressed seven transmembrane protein gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:16061724 1321335 Dcstamp dendrocyte expressed seven transmembrane protein gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:16061724 1321337 Sema4g sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21122816 1321337 Sema4g sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21122816 1321337 Sema4g sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:21122816 1321337 Sema4g sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G gene MP:0004041 increased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20161201 MGI PMID:25892012 1321337 Sema4g sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20161201 MGI PMID:25892012 1321337 Sema4g sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G gene MP:0009964 abnormal cerebellum lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:21122816 1321337 Sema4g sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20141003 MGI PMID:21122816 1321339 Ddx47 DEAD box helicase 47 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241010 MGI 1321339 Ddx47 DEAD box helicase 47 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1321339 Ddx47 DEAD box helicase 47 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241010 MGI 1321341 Rgs11 regulator of G-protein signaling 11 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:22547806 1321341 Rgs11 regulator of G-protein signaling 11 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22371490 1321341 Rgs11 regulator of G-protein signaling 11 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19535587 1321341 Rgs11 regulator of G-protein signaling 11 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22371490 1321341 Rgs11 regulator of G-protein signaling 11 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22547806 1321341 Rgs11 regulator of G-protein signaling 11 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19535587 1321341 Rgs11 regulator of G-protein signaling 11 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22371490 1321341 Rgs11 regulator of G-protein signaling 11 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19535587 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19004773 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19004773 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0000505 decreased digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:19004773 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0000507 absent digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:19004773 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0001314 cornea opacity IEA N RGD:5509061 20200514 MGI 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20230601 MGI 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20201022 MGI 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0004137 abnormal gastric surface mucous cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19004773 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19004773 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20150312 MGI PMID:19004773 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20141003 MGI PMID:19004773 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1321345 Slc26a9 solute carrier family 26, member 9 gene MP:0013566 dilated gastric gland IAGP N RGD:5509061 20150312 MGI PMID:19004773 1321353 Gemin5 gem nuclear organelle associated protein 5 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20240523 MGI 1321353 Gemin5 gem nuclear organelle associated protein 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321353 Gemin5 gem nuclear organelle associated protein 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1321355 Irf5 interferon regulatory factor 5 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20200402 MGI 1321355 Irf5 interferon regulatory factor 5 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22431588 1321355 Irf5 interferon regulatory factor 5 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111215 MGI 1321355 Irf5 interferon regulatory factor 5 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15665823 1321355 Irf5 interferon regulatory factor 5 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22431588 1321355 Irf5 interferon regulatory factor 5 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:22431588 1321355 Irf5 interferon regulatory factor 5 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:15665823 1321355 Irf5 interferon regulatory factor 5 gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22431588 1321355 Irf5 interferon regulatory factor 5 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:22431588 1321355 Irf5 interferon regulatory factor 5 gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:22431588 1321355 Irf5 interferon regulatory factor 5 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22431588 1321355 Irf5 interferon regulatory factor 5 gene MP:0008524 increased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22431588 1321355 Irf5 interferon regulatory factor 5 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15665823 1321355 Irf5 interferon regulatory factor 5 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22431588 1321355 Irf5 interferon regulatory factor 5 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:22431588 1321355 Irf5 interferon regulatory factor 5 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:15665823 1321355 Irf5 interferon regulatory factor 5 gene MP:0008648 decreased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:15665823 1321355 Irf5 interferon regulatory factor 5 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:22431588 1321355 Irf5 interferon regulatory factor 5 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:22431588 1321355 Irf5 interferon regulatory factor 5 gene MP:0010836 decreased CD4-positive, alpha-beta memory T cell number IEA N RGD:5509061 20201022 MGI 1321355 Irf5 interferon regulatory factor 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:20818394 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:20818394 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18195075 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:20818394 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18195075 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18195075 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:18195075 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:18195075 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:18195075 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:20818394 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18195075 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18195075 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20818394 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0008077 abnormal CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18195075 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:20818394 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:20818394 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0008397 abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18195075 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0008465 absent mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:20818394 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20181227 MGI 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:20818394 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:20818394 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0009634 absent popliteal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:20818394 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1321364 Tox thymocyte selection-associated high mobility group box gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1321366 Zfp513 zinc finger protein 513 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1321366 Zfp513 zinc finger protein 513 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1321366 Zfp513 zinc finger protein 513 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:15539150 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15539150 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15539150 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0002223 lymphoid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15539150 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18313334 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15539150 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18313334 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18313334 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008175 absent follicular B cells IAGP N RGD:5509061 20141003 MGI PMID:18313334 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21300983 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:15539150 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18313334 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:18313334 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18313334 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:21300983 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008523 absent lymph node germinal center IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15539150 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0013247 placenta necrosis IAGP N RGD:5509061 20190912 MGI PMID:29539633 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20160407 MGI PMID:9390694 1321368 Traf2 TNF receptor-associated factor 2 gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:29539633 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:10452377 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:23150788 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:11807038 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:12585968 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:10452377 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:11807038 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12585968 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23100430 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11807038 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10452377 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:15254021 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:23100430 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10452377 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15254021 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23100430 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:23100430 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12466504 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:10452377 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11807038 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15254021 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0001967 deafness IAGP N RGD:5509061 20170706 MGI PMID:25995473 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:23100430 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23100430 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111215 MGI 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0002623 abnormal vestibular hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23100430 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10452377 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20170706 MGI PMID:25995473 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:10452377 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:12585968 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:9735355 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20170706 MGI PMID:25995473 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0003151 absent tunnel of Corti IAGP N RGD:5509061 20141003 MGI PMID:23150788 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0003152 abnormal pillar cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12585968 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23150788 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:23150788 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0003986 small cochlear ganglion IAGP N RGD:5509061 20170706 MGI PMID:25995473 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:12585968 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004298 vestibular ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:12585968 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004298 vestibular ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004298 vestibular ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004298 vestibular ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:9735355 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004301 absent organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004301 absent organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004302 abnormal Deiters cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004306 small Rosenthal canal IAGP N RGD:5509061 20141003 MGI PMID:10452377 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004308 abnormal basilar membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:10452377 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004312 absent pillar cells IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9735355 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004325 absent vestibular hair cells IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004328 decreased vestibular hair cell number IAGP N RGD:5509061 20141003 MGI PMID:23100430 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15254021 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9735355 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20141003 MGI PMID:10452377 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15254021 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004397 absent cochlear inner hair cells IAGP N RGD:5509061 20170706 MGI PMID:25995473 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15254021 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12585968 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15254021 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004403 absent cochlear outer hair cells IAGP N RGD:5509061 20170706 MGI PMID:25995473 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15254021 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20210429 MGI PMID:32375046 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:10452377 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:23150788 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004409 abnormal crista ampullaris neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:10452377 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:23100430 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004518 absent vestibular hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004518 absent vestibular hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:9735355 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004526 absent cochlear hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:23150788 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004526 absent cochlear hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004526 absent cochlear hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004526 absent cochlear hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:9735355 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15254021 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004530 absent outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004535 absent inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:15254021 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004535 absent inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004586 pillar cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15254021 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004588 abnormal vestibular hair cell development IAGP N RGD:5509061 20141003 MGI PMID:12585968 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004588 abnormal vestibular hair cell development IAGP N RGD:5509061 20141003 MGI PMID:9735355 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004589 abnormal cochlear hair cell development IAGP N RGD:5509061 20141003 MGI PMID:12585968 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004589 abnormal cochlear hair cell development IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004590 absent Deiters cells IAGP N RGD:5509061 20141003 MGI PMID:12585968 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20210429 MGI PMID:32375046 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20170706 MGI PMID:25995473 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20170706 MGI PMID:25995473 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004741 mixed hearing loss IAGP N RGD:5509061 20170706 MGI PMID:25995473 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11807038 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:23100430 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:15254021 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23100430 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0006276 abnormal autonomic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12466504 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11807038 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:11807038 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20210429 MGI PMID:32375046 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20111116 MGI 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11807038 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0008105 increased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:11807038 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0008304 abnormal organ of Corti supporting cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10452377 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:11807038 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0010015 abnormal cuticular plate morphology IAGP N RGD:5509061 20141003 MGI PMID:23150788 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20171012 MGI PMID:12466504 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15254021 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:8637595 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:9256502 1321372 Pou4f3 POU domain, class 4, transcription factor 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20210429 MGI PMID:32375046 1321374 Fbxw2 F-box and WD-40 domain protein 2 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1321377 Rdh12 retinol dehydrogenase 12 gene MP:0003011 delayed dark adaptation IAGP N RGD:5509061 20141003 MGI PMID:17032653 1321377 Rdh12 retinol dehydrogenase 12 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:17032653 1321377 Rdh12 retinol dehydrogenase 12 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17032653 1321377 Rdh12 retinol dehydrogenase 12 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17032653 1321377 Rdh12 retinol dehydrogenase 12 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17130236 1321377 Rdh12 retinol dehydrogenase 12 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17032653 1321377 Rdh12 retinol dehydrogenase 12 gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:17032653 1321394 Srf serum response factor gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:15647354 1321394 Srf serum response factor gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:15169892 1321394 Srf serum response factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15169892 1321394 Srf serum response factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15569937 1321394 Srf serum response factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16260633 1321394 Srf serum response factor gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:15929941 1321394 Srf serum response factor gene MP:0000288 abnormal pericardium morphology IAGP N RGD:5509061 20141003 MGI PMID:15929941 1321394 Srf serum response factor gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:15929941 1321394 Srf serum response factor gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15169892 1321394 Srf serum response factor gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20150910 MGI PMID:18952847 1321394 Srf serum response factor gene MP:0000705 athymia IAGP N RGD:5509061 20150910 MGI PMID:18952847 1321394 Srf serum response factor gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17591768 1321394 Srf serum response factor gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:15647354 1321394 Srf serum response factor gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15647354 1321394 Srf serum response factor gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16260633 1321394 Srf serum response factor gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15169892 1321394 Srf serum response factor gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:15929941 1321394 Srf serum response factor gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15169892 1321394 Srf serum response factor gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9799237 1321394 Srf serum response factor gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:9799237 1321394 Srf serum response factor gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:15929941 1321394 Srf serum response factor gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:9799237 1321394 Srf serum response factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9799237 1321394 Srf serum response factor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15929941 1321394 Srf serum response factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15647354 1321394 Srf serum response factor gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:15647354 1321394 Srf serum response factor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16260633 1321394 Srf serum response factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11857797 1321394 Srf serum response factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15169892 1321394 Srf serum response factor gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:15169892 1321394 Srf serum response factor gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:15647354 1321394 Srf serum response factor gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20150910 MGI PMID:18952847 1321394 Srf serum response factor gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:15169892 1321394 Srf serum response factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:16260633 1321394 Srf serum response factor gene MP:0002976 vascular smooth muscle hypotrophy IAGP N RGD:5509061 20141003 MGI PMID:15569937 1321394 Srf serum response factor gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15647354 1321394 Srf serum response factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16260633 1321394 Srf serum response factor gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15929941 1321394 Srf serum response factor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15169892 1321394 Srf serum response factor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9799237 1321394 Srf serum response factor gene MP:0004032 abnormal interventricular groove morphology IAGP N RGD:5509061 20141003 MGI PMID:15929941 1321394 Srf serum response factor gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:16260633 1321394 Srf serum response factor gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:16260633 1321394 Srf serum response factor gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:15647354 1321394 Srf serum response factor gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:17591768 1321394 Srf serum response factor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17591768 1321394 Srf serum response factor gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17591768 1321394 Srf serum response factor gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:15647354 1321394 Srf serum response factor gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15929941 1321394 Srf serum response factor gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:15929941 1321394 Srf serum response factor gene MP:0005314 absent thyroid gland IAGP N RGD:5509061 20150910 MGI PMID:18952847 1321394 Srf serum response factor gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15929941 1321394 Srf serum response factor gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16260633 1321394 Srf serum response factor gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:15929941 1321394 Srf serum response factor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:16260633 1321394 Srf serum response factor gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:16260633 1321394 Srf serum response factor gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:16260633 1321394 Srf serum response factor gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17591768 1321394 Srf serum response factor gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17591768 1321394 Srf serum response factor gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17591768 1321394 Srf serum response factor gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:17591768 1321394 Srf serum response factor gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:15647354 1321394 Srf serum response factor gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20150910 MGI PMID:18952847 1321394 Srf serum response factor gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:16260633 1321394 Srf serum response factor gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:15169892 1321394 Srf serum response factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15647354 1321394 Srf serum response factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15647354 1321394 Srf serum response factor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15169892 1321394 Srf serum response factor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15929941 1321394 Srf serum response factor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20150910 MGI PMID:18952847 1321394 Srf serum response factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15569937 1321394 Srf serum response factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15929941 1321394 Srf serum response factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9799237 1321394 Srf serum response factor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:16260633 1321396 Chtf18 CTF18, chromosome transmission fidelity factor 18 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23133398 1321396 Chtf18 CTF18, chromosome transmission fidelity factor 18 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23133398 1321396 Chtf18 CTF18, chromosome transmission fidelity factor 18 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1321396 Chtf18 CTF18, chromosome transmission fidelity factor 18 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1321396 Chtf18 CTF18, chromosome transmission fidelity factor 18 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23133398 1321396 Chtf18 CTF18, chromosome transmission fidelity factor 18 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23133398 1321396 Chtf18 CTF18, chromosome transmission fidelity factor 18 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1321396 Chtf18 CTF18, chromosome transmission fidelity factor 18 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 1321396 Chtf18 CTF18, chromosome transmission fidelity factor 18 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23133398 1321396 Chtf18 CTF18, chromosome transmission fidelity factor 18 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23133398 1321396 Chtf18 CTF18, chromosome transmission fidelity factor 18 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220519 MGI 1321396 Chtf18 CTF18, chromosome transmission fidelity factor 18 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23133398 1321396 Chtf18 CTF18, chromosome transmission fidelity factor 18 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23133398 1321396 Chtf18 CTF18, chromosome transmission fidelity factor 18 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1321396 Chtf18 CTF18, chromosome transmission fidelity factor 18 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:23133398 1321398 Togaram1 TOG array regulator of axonemal microtubules 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20210520 MGI 1321398 Togaram1 TOG array regulator of axonemal microtubules 1 gene MP:0000562 polydactyly IEA N RGD:5509061 20210520 MGI 1321398 Togaram1 TOG array regulator of axonemal microtubules 1 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20210826 MGI 1321398 Togaram1 TOG array regulator of axonemal microtubules 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1321398 Togaram1 TOG array regulator of axonemal microtubules 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1321398 Togaram1 TOG array regulator of axonemal microtubules 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1321398 Togaram1 TOG array regulator of axonemal microtubules 1 gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20210826 MGI 1321398 Togaram1 TOG array regulator of axonemal microtubules 1 gene MP:0008797 facial cleft IEA N RGD:5509061 20210826 MGI 1321398 Togaram1 TOG array regulator of axonemal microtubules 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1321398 Togaram1 TOG array regulator of axonemal microtubules 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20210520 MGI 1321400 Hoga1 4-hydroxy-2-oxoglutarate aldolase 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20161117 MGI PMID:26428388 1321400 Hoga1 4-hydroxy-2-oxoglutarate aldolase 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 1321400 Hoga1 4-hydroxy-2-oxoglutarate aldolase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1321400 Hoga1 4-hydroxy-2-oxoglutarate aldolase 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20161117 MGI PMID:26428388 1321400 Hoga1 4-hydroxy-2-oxoglutarate aldolase 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20161117 MGI PMID:26428388 1321400 Hoga1 4-hydroxy-2-oxoglutarate aldolase 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20240523 MGI 1321405 Afg2a AFG2 AAA ATPase homolog A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230720 MGI 1321405 Afg2a AFG2 AAA ATPase homolog A gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20230720 MGI 1321405 Afg2a AFG2 AAA ATPase homolog A gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230720 MGI 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20181115 MGI PMID:24024552 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:17634284 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:17634284 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:17634284 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17634284 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20520781 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:17634284 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:17634284 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17634284 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17275357 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220317 MGI PMID:21208614 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17275357 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:17634284 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17634284 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17275357 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17275357 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220317 MGI PMID:21208614 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220317 MGI PMID:21208614 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17275357 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:17634284 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:20520781 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0004382 abnormal hair follicle melanogenesis IAGP N RGD:5509061 20181115 MGI PMID:24024552 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:17634284 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17634284 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0008732 reduced hair shaft melanin granule number IAGP N RGD:5509061 20181115 MGI PMID:24024552 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20520781 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220317 MGI PMID:21208614 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220317 MGI PMID:21208614 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0009233 enlarged sperm head IAGP N RGD:5509061 20220317 MGI PMID:21208614 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0009593 absent chorion IAGP N RGD:5509061 20141003 MGI PMID:17634284 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220317 MGI PMID:21208614 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20520781 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17634284 1321410 Hsp90b1 heat shock protein 90, beta (Grp94), member 1 gene MP:0011198 absent proamniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:17634284 1321414 Slc46a2 solute carrier family 46, member 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18684012 1321414 Slc46a2 solute carrier family 46, member 2 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18684012 1321414 Slc46a2 solute carrier family 46, member 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18684012 1321414 Slc46a2 solute carrier family 46, member 2 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18684012 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:16640660 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11884426 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9010048 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9620319 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:10910194 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:8299692 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:10319865 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:17986312 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11251123 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:11251123 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:15699117 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:17986312 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17986312 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22761313 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:10319865 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:8299692 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10319865 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:8299692 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:10319865 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11251123 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:8299692 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:9010048 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9010048 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9620319 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:9010048 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:9620319 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:9620319 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:9620319 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8299692 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002138 abnormal hepatobiliary system morphology IAGP N RGD:5509061 20141003 MGI PMID:9620319 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23023393 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:14764671 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17060023 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8299692 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:8299692 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:17060023 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11251123 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:23023393 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16640660 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8299692 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:10319865 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:11251123 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12810685 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:15699117 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:8299692 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:9620319 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20141003 MGI PMID:9620319 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0003254 bile duct inflammation IAGP N RGD:5509061 20141003 MGI PMID:9620319 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20141003 MGI PMID:9620319 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16640660 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:8299692 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22761313 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:23023393 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9620319 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:17060023 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16640660 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10319865 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:15699117 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:16640660 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10319865 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11251123 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15699117 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8299692 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008036 abnormal NK T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12810685 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:12810685 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:15699117 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:17060023 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:12810685 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12810685 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008201 absent follicular dendritic cells IAGP N RGD:5509061 20141003 MGI PMID:10319865 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008217 abnormal B cell activation IEA N RGD:5509061 20111116 MGI 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:10319865 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:15699117 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008397 abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14764671 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008397 abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17060023 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008465 absent mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11251123 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008471 abnormal spleen primary B follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10319865 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:11251123 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:12810685 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:12810685 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:9010048 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0008904 abnormal mammary fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:10910194 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0009297 decreased mammary fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10910194 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:14764671 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11251123 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0009629 small brachial lymph nodes IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11251123 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0009632 small axillary lymph nodes IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0009633 absent cervical lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11251123 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0009634 absent popliteal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11251123 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0009634 absent popliteal lymph nodes IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20170706 MGI PMID:26116508 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0013741 absent thymus corticomedullary boundary IAGP N RGD:5509061 20150430 MGI PMID:10319865 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0013741 absent thymus corticomedullary boundary IAGP N RGD:5509061 20150430 MGI PMID:8299692 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0014130 thymus cyst IAGP N RGD:5509061 20160324 MGI PMID:17986312 1321417 Map3k14 mitogen-activated protein kinase kinase kinase 14 gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:8299692 1321418 Syvn1 synovial apoptosis inhibitor 1, synoviolin gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20200310 MGI PMID:12975321 1321418 Syvn1 synovial apoptosis inhibitor 1, synoviolin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:24636985 1321418 Syvn1 synovial apoptosis inhibitor 1, synoviolin gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20200310 MGI PMID:12975321 1321418 Syvn1 synovial apoptosis inhibitor 1, synoviolin gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20200310 MGI PMID:12975321 1321418 Syvn1 synovial apoptosis inhibitor 1, synoviolin gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:12975321 1321418 Syvn1 synovial apoptosis inhibitor 1, synoviolin gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12975321 1321420 Nxn nucleoredoxin gene MP:0000111 cleft palate IEA N RGD:5509061 20160421 MGI 1321420 Nxn nucleoredoxin gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:20970343 1321420 Nxn nucleoredoxin gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170504 MGI 1321420 Nxn nucleoredoxin gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20160421 MGI 1321420 Nxn nucleoredoxin gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1321420 Nxn nucleoredoxin gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20160421 MGI 1321420 Nxn nucleoredoxin gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20160421 MGI 1321420 Nxn nucleoredoxin gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1321420 Nxn nucleoredoxin gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1321420 Nxn nucleoredoxin gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20201022 MGI 1321420 Nxn nucleoredoxin gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 1321420 Nxn nucleoredoxin gene MP:0001293 anophthalmia IEA N RGD:5509061 20170504 MGI 1321420 Nxn nucleoredoxin gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20200402 MGI 1321420 Nxn nucleoredoxin gene MP:0001340 abnormal eyelid morphology IEA N RGD:5509061 20160421 MGI 1321420 Nxn nucleoredoxin gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20211021 MGI 1321420 Nxn nucleoredoxin gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1321420 Nxn nucleoredoxin gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1321420 Nxn nucleoredoxin gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1321420 Nxn nucleoredoxin gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1321420 Nxn nucleoredoxin gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1321420 Nxn nucleoredoxin gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20201022 MGI 1321420 Nxn nucleoredoxin gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160421 MGI 1321420 Nxn nucleoredoxin gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20181227 MGI 1321420 Nxn nucleoredoxin gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:20970343 1321420 Nxn nucleoredoxin gene MP:0002764 short tibia IEA N RGD:5509061 20160421 MGI 1321420 Nxn nucleoredoxin gene MP:0002768 small adrenal glands IEA N RGD:5509061 20160811 MGI 1321420 Nxn nucleoredoxin gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1321420 Nxn nucleoredoxin gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20160811 MGI 1321420 Nxn nucleoredoxin gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1321420 Nxn nucleoredoxin gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:20970343 1321420 Nxn nucleoredoxin gene MP:0004377 small frontal bone IAGP N RGD:5509061 20141003 MGI PMID:20970343 1321420 Nxn nucleoredoxin gene MP:0004666 absent stapedial artery IEA N RGD:5509061 20170504 MGI 1321420 Nxn nucleoredoxin gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:20970343 1321420 Nxn nucleoredoxin gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:20970343 1321420 Nxn nucleoredoxin gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20210128 MGI 1321420 Nxn nucleoredoxin gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1321420 Nxn nucleoredoxin gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20970343 1321420 Nxn nucleoredoxin gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1321420 Nxn nucleoredoxin gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20201231 MGI 1321420 Nxn nucleoredoxin gene MP:0008797 facial cleft IEA N RGD:5509061 20210520 MGI 1321420 Nxn nucleoredoxin gene MP:0010052 increased grip strength IEA N RGD:5509061 20160804 MGI 1321420 Nxn nucleoredoxin gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20190502 MGI 1321420 Nxn nucleoredoxin gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20970343 1321420 Nxn nucleoredoxin gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20970343 1321420 Nxn nucleoredoxin gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1321420 Nxn nucleoredoxin gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20211021 MGI 1321420 Nxn nucleoredoxin gene MP:0010912 herniated liver IEA N RGD:5509061 20170504 MGI 1321420 Nxn nucleoredoxin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16466971 1321420 Nxn nucleoredoxin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20970343 1321420 Nxn nucleoredoxin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1321420 Nxn nucleoredoxin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1321420 Nxn nucleoredoxin gene MP:0011495 abnormal head shape IEA N RGD:5509061 20160811 MGI 1321420 Nxn nucleoredoxin gene MP:0011496 abnormal head size IEA N RGD:5509061 20160811 MGI 1321420 Nxn nucleoredoxin gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1321420 Nxn nucleoredoxin gene MP:0013916 decreased intestine length IEA N RGD:5509061 20170504 MGI 1321420 Nxn nucleoredoxin gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20170504 MGI 1321420 Nxn nucleoredoxin gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20211021 MGI 1321424 Grid2ip glutamate receptor, ionotropic, delta 2 (Grid2) interacting protein 1 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:18509461 1321424 Grid2ip glutamate receptor, ionotropic, delta 2 (Grid2) interacting protein 1 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:18509461 1321430 Sugp1 SURP and G patch domain containing 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1321430 Sugp1 SURP and G patch domain containing 1 gene MP:0000601 small liver IEA N RGD:5509061 20210128 MGI 1321430 Sugp1 SURP and G patch domain containing 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1321430 Sugp1 SURP and G patch domain containing 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1321430 Sugp1 SURP and G patch domain containing 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1321430 Sugp1 SURP and G patch domain containing 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1321430 Sugp1 SURP and G patch domain containing 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 1321430 Sugp1 SURP and G patch domain containing 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1321430 Sugp1 SURP and G patch domain containing 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1321430 Sugp1 SURP and G patch domain containing 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1321430 Sugp1 SURP and G patch domain containing 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1321430 Sugp1 SURP and G patch domain containing 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1321430 Sugp1 SURP and G patch domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1321430 Sugp1 SURP and G patch domain containing 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1321430 Sugp1 SURP and G patch domain containing 1 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20220519 MGI 1321432 Six6 sine oculis-related homeobox 6 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0001127 small ovary IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:12130660 1321432 Six6 sine oculis-related homeobox 6 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:12130660 1321432 Six6 sine oculis-related homeobox 6 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0002659 pituitary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12130660 1321432 Six6 sine oculis-related homeobox 6 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12130660 1321432 Six6 sine oculis-related homeobox 6 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12130660 1321432 Six6 sine oculis-related homeobox 6 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0008869 anovulation IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0009015 short proestrus IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0009047 short metestrus IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0010913 abnormal neuroendocrine cell morphology IAGP N RGD:5509061 20220203 MGI PMID:21228153 1321432 Six6 sine oculis-related homeobox 6 gene MP:0031436 decreased copulatory plug deposition IAGP N RGD:5509061 20220922 MGI PMID:21228153 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:11284712 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11284712 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:11284712 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11284712 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:11284712 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11284712 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:16556917 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11284712 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:16556917 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0004971 dermal hyperplasia IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:11284712 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20210429 MGI PMID:29649548 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0012546 triangular face IAGP N RGD:5509061 20141003 MGI PMID:11284712 1321434 Adamts2 ADAM metallopeptidase with thrombospondin type 1 motif 2 gene MP:0031395 cutaneous mastocytosis IAGP N RGD:5509061 20220721 MGI PMID:29649548 1321436 Gtf2h2 general transcription factor II H, polypeptide 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321438 Arid1a AT-rich interaction domain 1A gene MP:0000024 lowered ear position IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0000091 short premaxilla IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0000433 microcephaly IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0000445 short snout IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20160811 MGI PMID:25625625 1321438 Arid1a AT-rich interaction domain 1A gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160811 MGI PMID:25625625 1321438 Arid1a AT-rich interaction domain 1A gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:20522713 1321438 Arid1a AT-rich interaction domain 1A gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:18448678 1321438 Arid1a AT-rich interaction domain 1A gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:18448678 1321438 Arid1a AT-rich interaction domain 1A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18448678 1321438 Arid1a AT-rich interaction domain 1A gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18448678 1321438 Arid1a AT-rich interaction domain 1A gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20160811 MGI PMID:25625625 1321438 Arid1a AT-rich interaction domain 1A gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20522713 1321438 Arid1a AT-rich interaction domain 1A gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0005451 abnormal body composition IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0006198 enophthalmos IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20160811 MGI PMID:25625625 1321438 Arid1a AT-rich interaction domain 1A gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20160811 MGI PMID:25625625 1321438 Arid1a AT-rich interaction domain 1A gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0010565 absent fetal ductus arteriosus IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0010584 abnormal conotruncus septation IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20522713 1321438 Arid1a AT-rich interaction domain 1A gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18448678 1321438 Arid1a AT-rich interaction domain 1A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0012098 increased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:23129809 1321438 Arid1a AT-rich interaction domain 1A gene MP:0012747 abnormal cardiac neural crest cell morphology IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20160811 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20160811 MGI PMID:25625625 1321438 Arid1a AT-rich interaction domain 1A gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20171005 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0031554 abnormal aortic valve development IAGP N RGD:5509061 20240125 MGI PMID:26806701 1321438 Arid1a AT-rich interaction domain 1A gene MP:0031555 abnormal pulmonary valve development IAGP N RGD:5509061 20240125 MGI PMID:26806701 1321440 Ankrd10 ankyrin repeat domain 10 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1321440 Ankrd10 ankyrin repeat domain 10 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1321440 Ankrd10 ankyrin repeat domain 10 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1321440 Ankrd10 ankyrin repeat domain 10 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1321442 Phlda3 pleckstrin homology like domain, family A, member 3 gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:12032310 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20160804 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:14770179 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20141003 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0001314 cornea opacity IEA N RGD:5509061 20141003 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20141003 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0001391 abnormal tail movements IEA N RGD:5509061 20160804 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20141003 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20160804 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0002944 increased lactate dehydrogenase level IEA N RGD:5509061 20141003 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20141003 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20160804 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20160804 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20141003 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20141003 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0004917 abnormal T cell selection IAGP N RGD:5509061 20141003 MGI PMID:14770179 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:14770179 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0005014 increased B cell number IEA N RGD:5509061 20160804 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0005015 increased T cell number IEA N RGD:5509061 20160804 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:14770179 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20141003 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20141003 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20160804 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14770179 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14770179 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14770179 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0008211 decreased mature B cell number IEA N RGD:5509061 20160804 MGI 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:14770179 1321445 Elk4 ELK4, member of ETS oncogene family gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20160804 MGI 1321447 Osbp2 oxysterol binding protein 2 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20150205 MGI PMID:24245814 1321447 Osbp2 oxysterol binding protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20150205 MGI PMID:24245814 1321447 Osbp2 oxysterol binding protein 2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20150205 MGI PMID:24245814 1321447 Osbp2 oxysterol binding protein 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20150205 MGI PMID:24245814 1321447 Osbp2 oxysterol binding protein 2 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20150205 MGI PMID:24245814 1321447 Osbp2 oxysterol binding protein 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20150205 MGI PMID:24245814 1321447 Osbp2 oxysterol binding protein 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20150205 MGI PMID:24245814 1321447 Osbp2 oxysterol binding protein 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20150205 MGI PMID:24245814 1321447 Osbp2 oxysterol binding protein 2 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20150205 MGI PMID:24245814 1321447 Osbp2 oxysterol binding protein 2 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20150205 MGI PMID:24245814 1321447 Osbp2 oxysterol binding protein 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20150205 MGI PMID:24245814 1321447 Osbp2 oxysterol binding protein 2 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20150205 MGI PMID:24245814 1321447 Osbp2 oxysterol binding protein 2 gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20150205 MGI PMID:24245814 1321447 Osbp2 oxysterol binding protein 2 gene MP:0009852 increased Sertoli cell phagocytosis IAGP N RGD:5509061 20150205 MGI PMID:24245814 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0000111 cleft palate IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0003052 omphalocele IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0004025 polyploidy IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0004672 short ribs IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0005262 coloboma IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0009882 absent palatal shelf IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0011065 abnormal kidney epithelial cell primary cilium morphology IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0013214 decreased embryonic neuroepithelium primary cilium number IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20170202 MGI PMID:26965371 1321452 Ccp110 centriolar coiled coil protein 110 gene MP:0030320 abnormal temporal bone tympanic part morphology IAGP N RGD:5509061 20171109 MGI PMID:26965371 1321454 Cfhr1 complement factor H-related 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20230601 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0000111 cleft palate IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20170504 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0000520 absent kidney IEA N RGD:5509061 20170504 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20170504 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20170504 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0001914 hemorrhage IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0003078 aphakia IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0003722 absent ureter IEA N RGD:5509061 20170504 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0009495 abnormal common bile duct morphology IEA N RGD:5509061 20170504 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0009770 abnormal optic chiasm morphology IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0010053 decreased grip strength IEA N RGD:5509061 20150430 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20170504 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0013186 abnormal basilar artery morphology IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20171228 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1321455 Mybphl myosin binding protein H-like gene MP:0014017 abnormal Wolffian duct connection IEA N RGD:5509061 20170504 MGI 1321456 Mpv17l Mpv17 transgene, kidney disease mutant-like gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20220224 MGI PMID:34883249 1321456 Mpv17l Mpv17 transgene, kidney disease mutant-like gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20220224 MGI PMID:34883249 1321459 Nubp1 nucleotide binding protein 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:23028652 1321459 Nubp1 nucleotide binding protein 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:23028652 1321459 Nubp1 nucleotide binding protein 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:23028652 1321459 Nubp1 nucleotide binding protein 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:23028652 1321459 Nubp1 nucleotide binding protein 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23028652 1321459 Nubp1 nucleotide binding protein 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:23028652 1321459 Nubp1 nucleotide binding protein 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:23028652 1321459 Nubp1 nucleotide binding protein 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:23028652 1321459 Nubp1 nucleotide binding protein 1 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23028652 1321459 Nubp1 nucleotide binding protein 1 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:23028652 1321459 Nubp1 nucleotide binding protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23028652 1321462 Wtap WT1 associating protein gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17644066 1321462 Wtap WT1 associating protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17644066 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:20040491 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16705179 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:17082251 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20141003 MGI PMID:17082251 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:16705179 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:17082251 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16428452 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17082251 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0000935 abnormal folding of telencephalic vesicles IAGP N RGD:5509061 20141003 MGI PMID:17082251 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16705179 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20040491 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:20040491 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:20040491 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:20040491 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001705 abnormal proximal-distal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:20040491 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:20040491 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:20040491 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15831469 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16284942 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:16705179 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0002767 situs ambiguus IAGP N RGD:5509061 20141003 MGI PMID:16705179 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16705179 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:17082251 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0003639 abnormal response to vitamins IAGP N RGD:5509061 20141003 MGI PMID:16428452 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:20040491 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16705179 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:20040491 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:20040491 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:17082251 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0005163 cyclopia IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:20040491 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:17082251 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0006290 proboscis IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20040491 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17082251 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17082251 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0011192 decreased embryonic epiblast cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20040491 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0011525 abnormal placenta intervillous maternal lacunae morphology IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0011529 increased placenta intervillous maternal lacunae size IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0012258 philtrum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17082251 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0012523 abnormal upper lip morphology IAGP N RGD:5509061 20171019 MGI PMID:17082251 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:20040491 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0012706 decreased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20160929 MGI PMID:22383895 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0013227 small brain ventricles IAGP N RGD:5509061 20161103 MGI PMID:17082251 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0020903 increased middle ear goblet cell number IAGP N RGD:5509061 20191219 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0030066 short face IAGP N RGD:5509061 20170921 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20170928 MGI PMID:17082251 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0030226 middle ear polyps IAGP N RGD:5509061 20171019 MGI PMID:23459932 1321464 Tgif1 TGFB-induced factor homeobox 1 gene MP:0030410 middle ear effusion IAGP N RGD:5509061 20191219 MGI PMID:23459932 1321470 Ranbp1 RAN binding protein 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20190502 MGI 1321470 Ranbp1 RAN binding protein 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20190502 MGI 1321470 Ranbp1 RAN binding protein 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20190502 MGI 1321470 Ranbp1 RAN binding protein 1 gene MP:0000897 abnormal midbrain morphology IEA N RGD:5509061 20190502 MGI 1321470 Ranbp1 RAN binding protein 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21310149 1321470 Ranbp1 RAN binding protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21310149 1321470 Ranbp1 RAN binding protein 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1321470 Ranbp1 RAN binding protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21310149 1321470 Ranbp1 RAN binding protein 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1321470 Ranbp1 RAN binding protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21310149 1321470 Ranbp1 RAN binding protein 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20190502 MGI 1321470 Ranbp1 RAN binding protein 1 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:21310149 1321470 Ranbp1 RAN binding protein 1 gene MP:0005262 coloboma IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0006338 abnormal second pharyngeal arch morphology IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21310149 1321470 Ranbp1 RAN binding protein 1 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20221103 MGI 1321470 Ranbp1 RAN binding protein 1 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321470 Ranbp1 RAN binding protein 1 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20200604 MGI PMID:25452572 1321472 Scrib scribbled planar cell polarity gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:21515572 1321472 Scrib scribbled planar cell polarity gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:20215345 1321472 Scrib scribbled planar cell polarity gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20170105 MGI 1321472 Scrib scribbled planar cell polarity gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20181227 MGI 1321472 Scrib scribbled planar cell polarity gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:21515572 1321472 Scrib scribbled planar cell polarity gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:12112872 1321472 Scrib scribbled planar cell polarity gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:20215345 1321472 Scrib scribbled planar cell polarity gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15314648 1321472 Scrib scribbled planar cell polarity gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20181227 MGI 1321472 Scrib scribbled planar cell polarity gene MP:0000897 abnormal midbrain morphology IEA N RGD:5509061 20181227 MGI 1321472 Scrib scribbled planar cell polarity gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21515572 1321472 Scrib scribbled planar cell polarity gene MP:0000914 exencephaly IAGP N RGD:5509061 20151001 MGI PMID:25128525 1321472 Scrib scribbled planar cell polarity gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:15314648 1321472 Scrib scribbled planar cell polarity gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21515572 1321472 Scrib scribbled planar cell polarity gene MP:0000929 open neural tube IAGP N RGD:5509061 20151001 MGI PMID:25128525 1321472 Scrib scribbled planar cell polarity gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:24095903 1321472 Scrib scribbled planar cell polarity gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:24095903 1321472 Scrib scribbled planar cell polarity gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:24095903 1321472 Scrib scribbled planar cell polarity gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20151001 MGI PMID:25128525 1321472 Scrib scribbled planar cell polarity gene MP:0001341 absent eyelids IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0001406 abnormal gait IEA N RGD:5509061 20231207 MGI 1321472 Scrib scribbled planar cell polarity gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1321472 Scrib scribbled planar cell polarity gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20170105 MGI 1321472 Scrib scribbled planar cell polarity gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1321472 Scrib scribbled planar cell polarity gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20150618 MGI PMID:24276238 1321472 Scrib scribbled planar cell polarity gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20151001 MGI PMID:25128525 1321472 Scrib scribbled planar cell polarity gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20170105 MGI 1321472 Scrib scribbled planar cell polarity gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20151001 MGI PMID:25128525 1321472 Scrib scribbled planar cell polarity gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:12112872 1321472 Scrib scribbled planar cell polarity gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:11707073 1321472 Scrib scribbled planar cell polarity gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:12112872 1321472 Scrib scribbled planar cell polarity gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:21515572 1321472 Scrib scribbled planar cell polarity gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0003051 curly tail IAGP N RGD:5509061 20151001 MGI PMID:25128525 1321472 Scrib scribbled planar cell polarity gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:11707073 1321472 Scrib scribbled planar cell polarity gene MP:0003054 spina bifida IAGP N RGD:5509061 20151001 MGI PMID:25128525 1321472 Scrib scribbled planar cell polarity gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24095903 1321472 Scrib scribbled planar cell polarity gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20151001 MGI PMID:25128525 1321472 Scrib scribbled planar cell polarity gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:21559415 1321472 Scrib scribbled planar cell polarity gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20170105 MGI 1321472 Scrib scribbled planar cell polarity gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1321472 Scrib scribbled planar cell polarity gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12112872 1321472 Scrib scribbled planar cell polarity gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:12112872 1321472 Scrib scribbled planar cell polarity gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20170105 MGI 1321472 Scrib scribbled planar cell polarity gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15314648 1321472 Scrib scribbled planar cell polarity gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20215345 1321472 Scrib scribbled planar cell polarity gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20215345 1321472 Scrib scribbled planar cell polarity gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:20215345 1321472 Scrib scribbled planar cell polarity gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:21515572 1321472 Scrib scribbled planar cell polarity gene MP:0004961 increased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0005651 abnormal gonad rudiment morphology IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24095903 1321472 Scrib scribbled planar cell polarity gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20150618 MGI PMID:24276238 1321472 Scrib scribbled planar cell polarity gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20150618 MGI PMID:24276238 1321472 Scrib scribbled planar cell polarity gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:11707073 1321472 Scrib scribbled planar cell polarity gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:12112872 1321472 Scrib scribbled planar cell polarity gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:20215345 1321472 Scrib scribbled planar cell polarity gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:21515572 1321472 Scrib scribbled planar cell polarity gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:21559415 1321472 Scrib scribbled planar cell polarity gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20151001 MGI PMID:25128525 1321472 Scrib scribbled planar cell polarity gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20151001 MGI PMID:25128525 1321472 Scrib scribbled planar cell polarity gene MP:0009770 abnormal optic chiasm morphology IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1321472 Scrib scribbled planar cell polarity gene MP:0010945 lung epithelium hyperplasia IAGP N RGD:5509061 20150618 MGI PMID:24276238 1321472 Scrib scribbled planar cell polarity gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:21559415 1321472 Scrib scribbled planar cell polarity gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12112872 1321472 Scrib scribbled planar cell polarity gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21965329 1321472 Scrib scribbled planar cell polarity gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170105 MGI 1321472 Scrib scribbled planar cell polarity gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20151001 MGI PMID:25128525 1321472 Scrib scribbled planar cell polarity gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22586490 1321472 Scrib scribbled planar cell polarity gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22586490 1321472 Scrib scribbled planar cell polarity gene MP:0011964 increased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0012260 encephalomeningocele IAGP N RGD:5509061 20141003 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0012679 absent third ventricle IAGP N RGD:5509061 20160915 MGI PMID:10862153 1321472 Scrib scribbled planar cell polarity gene MP:0013765 iris hyperplasia IAGP N RGD:5509061 20150430 MGI PMID:24095903 1321478 Copa coatomer protein complex subunit alpha gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20220929 MGI PMID:32198142 1321478 Copa coatomer protein complex subunit alpha gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20220929 MGI PMID:32198142 1321478 Copa coatomer protein complex subunit alpha gene MP:0001861 lung inflammation IAGP N RGD:5509061 20220929 MGI PMID:32198142 1321478 Copa coatomer protein complex subunit alpha gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20220929 MGI PMID:32198142 1321478 Copa coatomer protein complex subunit alpha gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20220929 MGI PMID:32198142 1321478 Copa coatomer protein complex subunit alpha gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20220929 MGI PMID:32198142 1321478 Copa coatomer protein complex subunit alpha gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20220929 MGI PMID:32198142 1321478 Copa coatomer protein complex subunit alpha gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20220929 MGI PMID:32198142 1321478 Copa coatomer protein complex subunit alpha gene MP:0010998 pulmonary alveolar proteinosis IAGP N RGD:5509061 20220929 MGI PMID:32198142 1321478 Copa coatomer protein complex subunit alpha gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20220929 MGI PMID:32198142 1321478 Copa coatomer protein complex subunit alpha gene MP:0013772 increased effector memory T-helper cell number IAGP N RGD:5509061 20220929 MGI PMID:32198142 1321478 Copa coatomer protein complex subunit alpha gene MP:0031054 bronchiolitis IAGP N RGD:5509061 20220929 MGI PMID:32198142 1321478 Copa coatomer protein complex subunit alpha gene MP:0031238 reactive type II pneumocyte hyperplasia IAGP N RGD:5509061 20220929 MGI PMID:32198142 1321480 Ndn necdin, MAGE family member gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:11115855 1321480 Ndn necdin, MAGE family member gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16049186 1321480 Ndn necdin, MAGE family member gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17116257 1321480 Ndn necdin, MAGE family member gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17116257 1321480 Ndn necdin, MAGE family member gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17116257 1321480 Ndn necdin, MAGE family member gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:11115855 1321480 Ndn necdin, MAGE family member gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11115855 1321480 Ndn necdin, MAGE family member gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10508517 1321480 Ndn necdin, MAGE family member gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11115855 1321480 Ndn necdin, MAGE family member gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12629158 1321480 Ndn necdin, MAGE family member gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:12629158 1321480 Ndn necdin, MAGE family member gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10508517 1321480 Ndn necdin, MAGE family member gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11115855 1321480 Ndn necdin, MAGE family member gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12629158 1321480 Ndn necdin, MAGE family member gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:16049186 1321480 Ndn necdin, MAGE family member gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10508517 1321480 Ndn necdin, MAGE family member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10319852 1321480 Ndn necdin, MAGE family member gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17116257 1321480 Ndn necdin, MAGE family member gene MP:0002321 hypoventilation IAGP N RGD:5509061 20141003 MGI PMID:12629158 1321480 Ndn necdin, MAGE family member gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:10508517 1321480 Ndn necdin, MAGE family member gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:12629158 1321480 Ndn necdin, MAGE family member gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:16049186 1321480 Ndn necdin, MAGE family member gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:17116257 1321480 Ndn necdin, MAGE family member gene MP:0003880 abnormal central pattern generator function IAGP N RGD:5509061 20141003 MGI PMID:12629158 1321480 Ndn necdin, MAGE family member gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:17116257 1321480 Ndn necdin, MAGE family member gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:10508517 1321480 Ndn necdin, MAGE family member gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17116257 1321480 Ndn necdin, MAGE family member gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:12629158 1321480 Ndn necdin, MAGE family member gene MP:0006404 abnormal lumbar dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17116257 1321480 Ndn necdin, MAGE family member gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:10508517 1321480 Ndn necdin, MAGE family member gene MP:0010746 abnormal pre-Botzinger complex physiology IAGP N RGD:5509061 20141003 MGI PMID:12629158 1321480 Ndn necdin, MAGE family member gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12629158 1321480 Ndn necdin, MAGE family member gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11115855 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:11711676 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:11711676 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11711676 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:11711676 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11711676 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15705627 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11711676 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11711676 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11711676 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15705627 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11711676 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20141003 MGI PMID:11711676 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220210 MGI PMID:14724135 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11711676 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15705627 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220210 MGI PMID:14724135 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0009233 enlarged sperm head IAGP N RGD:5509061 20141003 MGI PMID:15705627 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20220210 MGI PMID:14724135 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20220210 MGI PMID:14724135 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20220210 MGI PMID:14724135 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20141003 MGI PMID:11711676 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220210 MGI PMID:14724135 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0009839 multiflagellated sperm IAGP N RGD:5509061 20141003 MGI PMID:15705627 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0030980 abnormal acroplaxome morphology IAGP N RGD:5509061 20220210 MGI PMID:14724135 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0031355 abnormal proacrosomal vesicle fusion IAGP N RGD:5509061 20220303 MGI PMID:11711676 1321482 Agfg1 ArfGAP with FG repeats 1 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20220428 MGI PMID:14724135 1321484 Rhoj ras homolog family member J gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20150122 MGI PMID:24434213 1321484 Rhoj ras homolog family member J gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20150122 MGI PMID:24434213 1321484 Rhoj ras homolog family member J gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22535667 1321484 Rhoj ras homolog family member J gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20150122 MGI PMID:24434213 1321484 Rhoj ras homolog family member J gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20150122 MGI PMID:24434213 1321484 Rhoj ras homolog family member J gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20150122 MGI PMID:24434213 1321484 Rhoj ras homolog family member J gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20150122 MGI PMID:24434213 1321484 Rhoj ras homolog family member J gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20150122 MGI PMID:24434213 1321484 Rhoj ras homolog family member J gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20150122 MGI PMID:24434213 1321486 Ap4b1 adaptor-related protein complex AP-4, beta 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18341993 1321486 Ap4b1 adaptor-related protein complex AP-4, beta 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18341993 1321487 Azi2 5-azacytidine induced gene 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23610142 1321487 Azi2 5-azacytidine induced gene 2 gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23610142 1321487 Azi2 5-azacytidine induced gene 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23610142 1321487 Azi2 5-azacytidine induced gene 2 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:23610142 1321487 Azi2 5-azacytidine induced gene 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:23610142 1321487 Azi2 5-azacytidine induced gene 2 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23610142 1321489 Pank3 pantothenate kinase 3 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1321489 Pank3 pantothenate kinase 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1321489 Pank3 pantothenate kinase 3 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1321489 Pank3 pantothenate kinase 3 gene MP:0004357 long tibia IEA N RGD:5509061 20221215 MGI 1321489 Pank3 pantothenate kinase 3 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1321489 Pank3 pantothenate kinase 3 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1321489 Pank3 pantothenate kinase 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22815849 1321495 Lpp LIM domain containing preferred translocation partner in lipoma gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:19111675 1321495 Lpp LIM domain containing preferred translocation partner in lipoma gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1321495 Lpp LIM domain containing preferred translocation partner in lipoma gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1321495 Lpp LIM domain containing preferred translocation partner in lipoma gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1321495 Lpp LIM domain containing preferred translocation partner in lipoma gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20230119 MGI 1321495 Lpp LIM domain containing preferred translocation partner in lipoma gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:19111675 1321495 Lpp LIM domain containing preferred translocation partner in lipoma gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:19111675 1321495 Lpp LIM domain containing preferred translocation partner in lipoma gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1321495 Lpp LIM domain containing preferred translocation partner in lipoma gene MP:0003959 abnormal lean body mass IEA N RGD:5509061 20240523 MGI 1321495 Lpp LIM domain containing preferred translocation partner in lipoma gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20240523 MGI 1321495 Lpp LIM domain containing preferred translocation partner in lipoma gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1321495 Lpp LIM domain containing preferred translocation partner in lipoma gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19111675 1321495 Lpp LIM domain containing preferred translocation partner in lipoma gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230119 MGI 1321496 Zfp787 zinc finger protein 787 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1321496 Zfp787 zinc finger protein 787 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20220519 MGI 1321496 Zfp787 zinc finger protein 787 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1321496 Zfp787 zinc finger protein 787 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 1321496 Zfp787 zinc finger protein 787 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20220811 MGI 1321496 Zfp787 zinc finger protein 787 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1321496 Zfp787 zinc finger protein 787 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1321496 Zfp787 zinc finger protein 787 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1321498 Ipo9 importin 9 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1321498 Ipo9 importin 9 gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20210520 MGI 1321498 Ipo9 importin 9 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1321498 Ipo9 importin 9 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20201022 MGI 1321498 Ipo9 importin 9 gene MP:0001726 abnormal allantois morphology IEA N RGD:5509061 20201022 MGI 1321498 Ipo9 importin 9 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1321498 Ipo9 importin 9 gene MP:0002824 abnormal chorioallantoic fusion IEA N RGD:5509061 20201022 MGI 1321498 Ipo9 importin 9 gene MP:0002861 abnormal tail bud morphology IEA N RGD:5509061 20201022 MGI 1321498 Ipo9 importin 9 gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20201022 MGI 1321498 Ipo9 importin 9 gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20201022 MGI 1321498 Ipo9 importin 9 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20201022 MGI 1321498 Ipo9 importin 9 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20201022 MGI 1321498 Ipo9 importin 9 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20201022 MGI 1321498 Ipo9 importin 9 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1321498 Ipo9 importin 9 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20201022 MGI 1321498 Ipo9 importin 9 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20141003 MGI 1321498 Ipo9 importin 9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321498 Ipo9 importin 9 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1321501 Hoxc12 homeobox C12 gene MP:0000745 tremors IEA N RGD:5509061 20201022 MGI 1321501 Hoxc12 homeobox C12 gene MP:0011999 abnormal tail length IEA N RGD:5509061 20201022 MGI 1321501 Hoxc12 homeobox C12 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1321502 Tmem115 transmembrane protein 115 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1321502 Tmem115 transmembrane protein 115 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20220519 MGI 1321502 Tmem115 transmembrane protein 115 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220811 MGI 1321502 Tmem115 transmembrane protein 115 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220519 MGI 1321502 Tmem115 transmembrane protein 115 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321507 Ppox protoporphyrinogen oxidase gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1321507 Ppox protoporphyrinogen oxidase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210128 MGI 1321507 Ppox protoporphyrinogen oxidase gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1321507 Ppox protoporphyrinogen oxidase gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20151210 MGI PMID:11929050 1321507 Ppox protoporphyrinogen oxidase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1321507 Ppox protoporphyrinogen oxidase gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1321507 Ppox protoporphyrinogen oxidase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20151210 MGI PMID:11929050 1321507 Ppox protoporphyrinogen oxidase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20151210 MGI PMID:11929050 1321507 Ppox protoporphyrinogen oxidase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20151210 MGI PMID:11929050 1321507 Ppox protoporphyrinogen oxidase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1321507 Ppox protoporphyrinogen oxidase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1321509 Plekhf1 pleckstrin homology domain containing, family F (with FYVE domain) member 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20191003 MGI PMID:31189603 1321509 Plekhf1 pleckstrin homology domain containing, family F (with FYVE domain) member 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20191003 MGI PMID:31189603 1321509 Plekhf1 pleckstrin homology domain containing, family F (with FYVE domain) member 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20191003 MGI PMID:31189603 1321509 Plekhf1 pleckstrin homology domain containing, family F (with FYVE domain) member 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20191003 MGI PMID:31189603 1321509 Plekhf1 pleckstrin homology domain containing, family F (with FYVE domain) member 1 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20191003 MGI PMID:31189603 1321509 Plekhf1 pleckstrin homology domain containing, family F (with FYVE domain) member 1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20191003 MGI PMID:31189603 1321509 Plekhf1 pleckstrin homology domain containing, family F (with FYVE domain) member 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20191003 MGI PMID:31189603 1321509 Plekhf1 pleckstrin homology domain containing, family F (with FYVE domain) member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321509 Plekhf1 pleckstrin homology domain containing, family F (with FYVE domain) member 1 gene MP:0030951 abnormal endocytosis IAGP N RGD:5509061 20191003 MGI PMID:31189603 1321514 Hps3 HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:2379821 1321514 Hps3 HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:3408670 1321514 Hps3 HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:2379821 1321514 Hps3 HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 gene MP:0002551 abnormal blood coagulation IEA N RGD:5509061 20111116 MGI 1321514 Hps3 HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:3408670 1321514 Hps3 HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:12445206 1321514 Hps3 HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 gene MP:0005100 abnormal choroid pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11707070 1321514 Hps3 HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18715234 1321514 Hps3 HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11707070 1321514 Hps3 HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:3408670 1321514 Hps3 HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 gene MP:0008480 absent eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:3408670 1321514 Hps3 HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20170803 MGI PMID:3408670 1321514 Hps3 HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20170803 MGI PMID:3408670 1321514 Hps3 HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:3408670 1321514 Hps3 HPS3, biogenesis of lysosomal organelles complex 2 subunit 1 gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170720 MGI PMID:3408670 1321516 Cog4 component of oligomeric golgi complex 4 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200514 MGI 1321516 Cog4 component of oligomeric golgi complex 4 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1321516 Cog4 component of oligomeric golgi complex 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321516 Cog4 component of oligomeric golgi complex 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1321520 Tulp2 TUB like protein 2 gene MP:0001304 cataract IEA N RGD:5509061 20210520 MGI 1321520 Tulp2 TUB like protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20210805 MGI PMID:33763418 1321520 Tulp2 TUB like protein 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210805 MGI PMID:33763418 1321520 Tulp2 TUB like protein 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210805 MGI PMID:33763418 1321520 Tulp2 TUB like protein 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1321520 Tulp2 TUB like protein 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210805 MGI PMID:33763418 1321520 Tulp2 TUB like protein 2 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20210805 MGI PMID:33763418 1321520 Tulp2 TUB like protein 2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20210805 MGI PMID:33763418 1321520 Tulp2 TUB like protein 2 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20210805 MGI PMID:33763418 1321520 Tulp2 TUB like protein 2 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20210805 MGI PMID:33763418 1321520 Tulp2 TUB like protein 2 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20210805 MGI PMID:33763418 1321520 Tulp2 TUB like protein 2 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210805 MGI PMID:33763418 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0000274 enlarged heart IEA N RGD:5509061 20160811 MGI 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0000691 enlarged spleen IEA N RGD:5509061 20160811 MGI 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11114376 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160421 MGI 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0004041 increased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20161201 MGI PMID:25892012 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0004940 abnormal B-1 B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11114376 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11114376 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11114376 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11114376 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11114376 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:11114376 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:11114376 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20161201 MGI PMID:25892012 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1321524 Sema4d sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1321526 Prpf3 pre-mRNA processing factor 3 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1321526 Prpf3 pre-mRNA processing factor 3 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:20811066 1321526 Prpf3 pre-mRNA processing factor 3 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20811066 1321526 Prpf3 pre-mRNA processing factor 3 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20811066 1321526 Prpf3 pre-mRNA processing factor 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18552388 1321526 Prpf3 pre-mRNA processing factor 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321526 Prpf3 pre-mRNA processing factor 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1321526 Prpf3 pre-mRNA processing factor 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17591855 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:15466160 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18547789 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18547789 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17336907 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:18547789 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:15466160 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:17080428 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000371 diluted coat color IAGP N RGD:5509061 20190103 MGI PMID:16651378 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15959515 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:15959515 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12039915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:12039915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:17360543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19897741 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:12593800 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:12593800 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:16581056 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001280 loss of vibrissae IAGP N RGD:5509061 20141003 MGI PMID:12593800 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:17360543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:17360543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15466160 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:18635610 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:15466160 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18635610 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:21168915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17658279 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12039915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17591855 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:18635610 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17360543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11967543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12039915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18198335 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141225 MGI 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:17336907 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:17360543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17360543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12039915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11967543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:22146645 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20181122 MGI PMID:21493891 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20240530 MGI PMID:28395734 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17591855 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20240530 MGI PMID:28395734 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20181122 MGI PMID:21493891 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20141003 MGI PMID:18198335 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0003247 abnormal glutaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18198335 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0003359 hypaxial muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17360543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:12593800 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:16581056 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20639863 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15959515 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17336907 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:17360543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220915 MGI PMID:30213224 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:18635610 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15466160 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15466160 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:18635610 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0004248 abnormal epaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17360543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20190103 MGI PMID:16651378 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0004382 abnormal hair follicle melanogenesis IAGP N RGD:5509061 20190103 MGI PMID:16651378 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17229764 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15466160 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0004786 abnormal common cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15466160 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15466160 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21168915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:18198335 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12039915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17591855 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21168915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17658279 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12593800 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12039915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17984302 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12039915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005114 premature hair loss IAGP N RGD:5509061 20141003 MGI PMID:12593800 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20181122 MGI PMID:21493891 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20190103 MGI PMID:16651378 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:15466160 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17336907 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20181227 MGI 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21168915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:17591855 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:21168915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20141003 MGI PMID:15466160 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:16581056 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:21168915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12039915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15137944 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:17591855 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008137 absent podocytes IAGP N RGD:5509061 20141003 MGI PMID:17229764 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:11967543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:12039915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:17457934 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:11967543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12039915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17457934 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008200 decreased follicular dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:17591855 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11967543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008524 increased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:17591855 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:17658279 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15466160 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:18547789 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0009149 decreased pancreatic acinar cell number IAGP N RGD:5509061 20141003 MGI PMID:18635610 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0009159 increased pancreatic acinar cell number IAGP N RGD:5509061 20141003 MGI PMID:22146645 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:18635610 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:18635610 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0009179 abnormal pancreatic alpha cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18635610 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:18635610 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:21168915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0009408 decreased skeletal muscle fiber density IAGP N RGD:5509061 20141003 MGI PMID:17360543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20190103 MGI PMID:16651378 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11967543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18198335 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0010171 abnormal centroacinar cell of Langerhans morphology IAGP N RGD:5509061 20141003 MGI PMID:22146645 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0010183 abnormal CD4-positive helper T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21168915 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0010198 decreased lymphatic vessel endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:20360386 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20181122 MGI PMID:21493891 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0010942 abnormal respiratory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19502490 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0011071 absent club cells IAGP N RGD:5509061 20141003 MGI PMID:19502490 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18635610 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17360543 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19897741 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18635610 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10476967 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17229764 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20360386 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20181122 MGI PMID:21493891 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20190103 MGI PMID:16651378 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:15466160 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0021095 abnormal dorsal interneuron 4 morphology IAGP N RGD:5509061 20220310 MGI PMID:18198335 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0031124 aortic valve inflammation IAGP N RGD:5509061 20200917 MGI PMID:21493891 1321530 Rbpj recombination signal binding protein for immunoglobulin kappa J region gene MP:0031518 calcified aortic valve cusp IAGP N RGD:5509061 20240118 MGI PMID:21493891 1321540 Ccl9 C-C motif chemokine ligand 9 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1321540 Ccl9 C-C motif chemokine ligand 9 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1321540 Ccl9 C-C motif chemokine ligand 9 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1321540 Ccl9 C-C motif chemokine ligand 9 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1321542 Plxnb1 plexin B1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20161222 MGI PMID:26579598 1321542 Plxnb1 plexin B1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20161222 MGI PMID:26579598 1321542 Plxnb1 plexin B1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20161222 MGI PMID:21035938 1321542 Plxnb1 plexin B1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17519029 1321542 Plxnb1 plexin B1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20161222 MGI PMID:26579598 1321542 Plxnb1 plexin B1 gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20161222 MGI PMID:26579598 1321542 Plxnb1 plexin B1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:18799546 1321542 Plxnb1 plexin B1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20161222 MGI PMID:21035938 1321542 Plxnb1 plexin B1 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20161222 MGI PMID:26579598 1321542 Plxnb1 plexin B1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20161222 MGI PMID:21035938 1321542 Plxnb1 plexin B1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20161222 MGI PMID:26579598 1321542 Plxnb1 plexin B1 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20161222 MGI PMID:26579598 1321542 Plxnb1 plexin B1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20161222 MGI PMID:26579598 1321542 Plxnb1 plexin B1 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20161222 MGI PMID:26579598 1321542 Plxnb1 plexin B1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20161222 MGI PMID:26579598 1321542 Plxnb1 plexin B1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20161222 MGI PMID:21035938 1321542 Plxnb1 plexin B1 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20161201 MGI PMID:25892012 1321542 Plxnb1 plexin B1 gene MP:0010981 abnormal branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:18799546 1321542 Plxnb1 plexin B1 gene MP:0010981 abnormal branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20161222 MGI PMID:21035938 1321542 Plxnb1 plexin B1 gene MP:0011364 abnormal metanephros morphology IAGP N RGD:5509061 20141003 MGI PMID:18799546 1321542 Plxnb1 plexin B1 gene MP:0011761 abnormal ureteric bud trunk morphology IAGP N RGD:5509061 20161222 MGI PMID:21035938 1321542 Plxnb1 plexin B1 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20161222 MGI PMID:26579598 1321546 Tmem17 transmembrane protein 17 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20240523 MGI 1321546 Tmem17 transmembrane protein 17 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20240523 MGI 1321546 Tmem17 transmembrane protein 17 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20240523 MGI 1321546 Tmem17 transmembrane protein 17 gene MP:0001914 hemorrhage IEA N RGD:5509061 20240523 MGI 1321546 Tmem17 transmembrane protein 17 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 1321548 Dgcr2 DiGeorge syndrome critical region gene 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1321548 Dgcr2 DiGeorge syndrome critical region gene 2 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20201231 MGI 1321548 Dgcr2 DiGeorge syndrome critical region gene 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230601 MGI 1321548 Dgcr2 DiGeorge syndrome critical region gene 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1321555 Tpgs2 tubulin polyglutamylase complex subunit 2 gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20240523 MGI 1321555 Tpgs2 tubulin polyglutamylase complex subunit 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1321555 Tpgs2 tubulin polyglutamylase complex subunit 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1321555 Tpgs2 tubulin polyglutamylase complex subunit 2 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1321555 Tpgs2 tubulin polyglutamylase complex subunit 2 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20210128 MGI 1321555 Tpgs2 tubulin polyglutamylase complex subunit 2 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20240523 MGI 1321555 Tpgs2 tubulin polyglutamylase complex subunit 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1321555 Tpgs2 tubulin polyglutamylase complex subunit 2 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20240523 MGI 1321555 Tpgs2 tubulin polyglutamylase complex subunit 2 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20240523 MGI 1321555 Tpgs2 tubulin polyglutamylase complex subunit 2 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20160421 MGI 1321555 Tpgs2 tubulin polyglutamylase complex subunit 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1321556 Mgat4d MGAT4 family, member C gene MP:0000467 abnormal esophagus morphology IEA N RGD:5509061 20161201 MGI 1321556 Mgat4d MGAT4 family, member C gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20161201 MGI 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11886853 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11886853 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0000962 disorganized dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:11886853 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12139926 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:8643673 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:8643673 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11886853 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11886853 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:8643673 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:11886853 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:11886853 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12139926 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:11886853 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11886853 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11886853 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:11886853 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11886853 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11886853 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1321559 Prkacb protein kinase, cAMP dependent, catalytic, beta gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11886853 1321561 Ch25h cholesterol 25-hydroxylase gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20181227 MGI 1321561 Ch25h cholesterol 25-hydroxylase gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1321561 Ch25h cholesterol 25-hydroxylase gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1321561 Ch25h cholesterol 25-hydroxylase gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:19805370 1321561 Ch25h cholesterol 25-hydroxylase gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:19805370 1321561 Ch25h cholesterol 25-hydroxylase gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:19805370 1321561 Ch25h cholesterol 25-hydroxylase gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:19805370 1321564 Vmn2r81 vomeronasal 2, receptor 81 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21112400 1321564 Vmn2r81 vomeronasal 2, receptor 81 gene MP:0002243 abnormal vomeronasal organ morphology IAGP N RGD:5509061 20141003 MGI PMID:21112400 1321564 Vmn2r81 vomeronasal 2, receptor 81 gene MP:0011678 abnormal vomeronasal sensory neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:24719092 1321564 Vmn2r81 vomeronasal 2, receptor 81 gene MP:0011679 abnormal vomeronasal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:24719092 1321566 Cdr2 cerebellar degeneration-related 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111215 MGI 1321570 B3gnt7 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1321570 B3gnt7 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1321570 B3gnt7 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20180628 MGI PMID:29625490 1321570 B3gnt7 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20231207 MGI 1321570 B3gnt7 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20180628 MGI PMID:29625490 1321570 B3gnt7 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20180628 MGI PMID:29625490 1321572 Nptx1 neuronal pentraxin 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:16763034 1321572 Nptx1 neuronal pentraxin 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16763034 1321574 Tekt3 tektin 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:18951373 1321574 Tekt3 tektin 3 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18951373 1321574 Tekt3 tektin 3 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:18951373 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20180426 MGI PMID:28287403 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20160128 MGI PMID:25705883 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20160128 MGI PMID:25705883 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20160128 MGI PMID:25705883 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:17283041 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:17283041 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20160128 MGI PMID:25705883 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18846253 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18846253 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:18846253 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17283041 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20160128 MGI PMID:25705883 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20160128 MGI PMID:25705883 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:16809760 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:17283041 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16809760 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17283041 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0002764 short tibia IEA N RGD:5509061 20160421 MGI 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16809760 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20180426 MGI PMID:28287403 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0003865 lymph node inflammation IAGP N RGD:5509061 20141003 MGI PMID:18846253 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20180426 MGI PMID:28287403 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:17283041 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:18846253 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16809760 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17283041 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0005190 osteomyelitis IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20160128 MGI PMID:25705883 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20180426 MGI PMID:28287403 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17283041 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:17283041 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17283041 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:17283041 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:18846253 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:17283041 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:17283041 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20160128 MGI PMID:25705883 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20160128 MGI PMID:25705883 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20160128 MGI PMID:25705883 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20160128 MGI PMID:25705883 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20160128 MGI PMID:25705883 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008704 abnormal interleukin-6 secretion IAGP N RGD:5509061 20160128 MGI PMID:25705883 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17283041 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20180426 MGI PMID:28287403 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20160128 MGI PMID:25705883 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20180426 MGI PMID:28287403 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20180426 MGI PMID:28287403 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0013123 head/neck swellings IAGP N RGD:5509061 20160128 MGI PMID:25705883 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0030466 alveolar process atrophy IAGP N RGD:5509061 20171221 MGI PMID:17218256 1321584 Sh3bp2 SH3-domain binding protein 2 gene MP:0030987 spinal cord inflammation IAGP N RGD:5509061 20191128 MGI PMID:17218256 1321588 Eps8 epidermal growth factor receptor pathway substrate 8 gene MP:0001987 alcohol preference IAGP N RGD:5509061 20141003 MGI PMID:17018287 1321588 Eps8 epidermal growth factor receptor pathway substrate 8 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17018287 1321588 Eps8 epidermal growth factor receptor pathway substrate 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10499589 1321588 Eps8 epidermal growth factor receptor pathway substrate 8 gene MP:0002863 improved righting response IAGP N RGD:5509061 20141003 MGI PMID:17018287 1321588 Eps8 epidermal growth factor receptor pathway substrate 8 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17018287 1321588 Eps8 epidermal growth factor receptor pathway substrate 8 gene MP:0003234 enhanced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17018287 1321588 Eps8 epidermal growth factor receptor pathway substrate 8 gene MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:17018287 1321588 Eps8 epidermal growth factor receptor pathway substrate 8 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:23918390 1321588 Eps8 epidermal growth factor receptor pathway substrate 8 gene MP:0004524 short cochlear hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:23918390 1321588 Eps8 epidermal growth factor receptor pathway substrate 8 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17018287 1321590 Ints8 integrator complex subunit 8 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1321590 Ints8 integrator complex subunit 8 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1321590 Ints8 integrator complex subunit 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1321590 Ints8 integrator complex subunit 8 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230119 MGI 1321594 Pla2g4e phospholipase A2, group IVE gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20230330 MGI PMID:35478358 1321594 Pla2g4e phospholipase A2, group IVE gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201231 MGI 1321594 Pla2g4e phospholipase A2, group IVE gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20230330 MGI PMID:35478358 1321594 Pla2g4e phospholipase A2, group IVE gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20230330 MGI PMID:35478358 1321594 Pla2g4e phospholipase A2, group IVE gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1321594 Pla2g4e phospholipase A2, group IVE gene MP:0012572 increased susceptibility to chemically induced skin inflammation IAGP N RGD:5509061 20230330 MGI PMID:35478358 1321598 Ms4a3 membrane-spanning 4-domains, subfamily A, member 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1321598 Ms4a3 membrane-spanning 4-domains, subfamily A, member 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1321598 Ms4a3 membrane-spanning 4-domains, subfamily A, member 3 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1321601 Rad54l RAD54 like (S. cerevisiae) gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:16428451 1321601 Rad54l RAD54 like (S. cerevisiae) gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16009599 1321601 Rad54l RAD54 like (S. cerevisiae) gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16428451 1321601 Rad54l RAD54 like (S. cerevisiae) gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:16009599 1321601 Rad54l RAD54 like (S. cerevisiae) gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20230824 MGI PMID:12897131 1321601 Rad54l RAD54 like (S. cerevisiae) gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12727892 1321601 Rad54l RAD54 like (S. cerevisiae) gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16428451 1321601 Rad54l RAD54 like (S. cerevisiae) gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16009599 1321601 Rad54l RAD54 like (S. cerevisiae) gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16428451 1321601 Rad54l RAD54 like (S. cerevisiae) gene MP:0012121 sclerocornea IEA N RGD:5509061 20190502 MGI 1321601 Rad54l RAD54 like (S. cerevisiae) gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20230824 MGI PMID:12897131 1321608 Slc27a3 solute carrier family 27 (fatty acid transporter), member 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1321608 Slc27a3 solute carrier family 27 (fatty acid transporter), member 3 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 1321608 Slc27a3 solute carrier family 27 (fatty acid transporter), member 3 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1321608 Slc27a3 solute carrier family 27 (fatty acid transporter), member 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1321608 Slc27a3 solute carrier family 27 (fatty acid transporter), member 3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1321609 Ergic2 ERGIC and golgi 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20240229 MGI PMID:34994051 1321609 Ergic2 ERGIC and golgi 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1321609 Ergic2 ERGIC and golgi 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1321609 Ergic2 ERGIC and golgi 2 gene MP:0004357 long tibia IEA N RGD:5509061 20211021 MGI 1321609 Ergic2 ERGIC and golgi 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20240229 MGI PMID:34994051 1321609 Ergic2 ERGIC and golgi 2 gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20240229 MGI PMID:34994051 1321609 Ergic2 ERGIC and golgi 2 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20240229 MGI PMID:34994051 1321609 Ergic2 ERGIC and golgi 2 gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20240229 MGI PMID:34994051 1321609 Ergic2 ERGIC and golgi 2 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1321609 Ergic2 ERGIC and golgi 2 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20240229 MGI PMID:34994051 1321609 Ergic2 ERGIC and golgi 2 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20240229 MGI PMID:34994051 1321609 Ergic2 ERGIC and golgi 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1321616 Anp32e acidic nuclear phosphoprotein 32 family member E gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20844742 1321616 Anp32e acidic nuclear phosphoprotein 32 family member E gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20844742 1321616 Anp32e acidic nuclear phosphoprotein 32 family member E gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21049064 1321616 Anp32e acidic nuclear phosphoprotein 32 family member E gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21636789 1321616 Anp32e acidic nuclear phosphoprotein 32 family member E gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21636789 1321619 Creld2 cysteine-rich with EGF-like domains 2 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20230511 MGI PMID:34549824 1321619 Creld2 cysteine-rich with EGF-like domains 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20230511 MGI PMID:34549824 1321619 Creld2 cysteine-rich with EGF-like domains 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230511 MGI PMID:34549824 1321619 Creld2 cysteine-rich with EGF-like domains 2 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1321619 Creld2 cysteine-rich with EGF-like domains 2 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20211021 MGI 1321619 Creld2 cysteine-rich with EGF-like domains 2 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20230511 MGI PMID:34549824 1321619 Creld2 cysteine-rich with EGF-like domains 2 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20230511 MGI PMID:34549824 1321619 Creld2 cysteine-rich with EGF-like domains 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20230511 MGI PMID:34549824 1321619 Creld2 cysteine-rich with EGF-like domains 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20230511 MGI PMID:34549824 1321619 Creld2 cysteine-rich with EGF-like domains 2 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20230511 MGI PMID:34549824 1321619 Creld2 cysteine-rich with EGF-like domains 2 gene MP:0020582 increased ceramide level IAGP N RGD:5509061 20230511 MGI PMID:34549824 1321619 Creld2 cysteine-rich with EGF-like domains 2 gene MP:0031265 increased susceptibility to hepatic steatosis IAGP N RGD:5509061 20230511 MGI PMID:34549824 1321619 Creld2 cysteine-rich with EGF-like domains 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20230511 MGI PMID:34549824 1321619 Creld2 cysteine-rich with EGF-like domains 2 gene MP:0031271 increased susceptibility to age-related hepatic steatosis IAGP N RGD:5509061 20230511 MGI PMID:34549824 1321621 Mccc1 methylcrotonoyl-Coenzyme A carboxylase 1 (alpha) gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200402 MGI 1321621 Mccc1 methylcrotonoyl-Coenzyme A carboxylase 1 (alpha) gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210520 MGI 1321621 Mccc1 methylcrotonoyl-Coenzyme A carboxylase 1 (alpha) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321621 Mccc1 methylcrotonoyl-Coenzyme A carboxylase 1 (alpha) gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1321624 Aars2 alanyl-tRNA synthetase 2, mitochondrial gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1321624 Aars2 alanyl-tRNA synthetase 2, mitochondrial gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201231 MGI 1321624 Aars2 alanyl-tRNA synthetase 2, mitochondrial gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20191107 MGI PMID:29228266 1321624 Aars2 alanyl-tRNA synthetase 2, mitochondrial gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20191107 MGI PMID:29228266 1321624 Aars2 alanyl-tRNA synthetase 2, mitochondrial gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1321624 Aars2 alanyl-tRNA synthetase 2, mitochondrial gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20211021 MGI 1321624 Aars2 alanyl-tRNA synthetase 2, mitochondrial gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1321624 Aars2 alanyl-tRNA synthetase 2, mitochondrial gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20240523 MGI 1321624 Aars2 alanyl-tRNA synthetase 2, mitochondrial gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1321624 Aars2 alanyl-tRNA synthetase 2, mitochondrial gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20191107 MGI PMID:29228266 1321624 Aars2 alanyl-tRNA synthetase 2, mitochondrial gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180712 MGI PMID:28008940 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20180712 MGI PMID:28008940 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20180712 MGI PMID:28008940 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20180712 MGI PMID:28008940 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20180712 MGI PMID:28008940 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180712 MGI PMID:28008940 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220428 MGI PMID:28008940 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20180712 MGI PMID:28008940 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20220428 MGI PMID:28008940 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20180712 MGI PMID:28008940 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20180712 MGI PMID:28008940 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20180712 MGI PMID:28008940 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20180712 MGI PMID:28008940 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0013410 decreased dendritic epidermal T cell number IEA N RGD:5509061 20201231 MGI 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220428 MGI PMID:28008940 1321626 Mkrn2 makorin, ring finger protein, 2 gene MP:0031389 abnormal ectoplasmic specialization morphology IAGP N RGD:5509061 20220428 MGI PMID:28008940 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:23028982 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0002985 abnormal urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:16174750 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:16174750 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0003017 decreased circulating bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:16174750 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0003031 acidosis IAGP N RGD:5509061 20141003 MGI PMID:16174750 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0003144 decreased otolith number IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0003462 abnormal response to novel odor IAGP N RGD:5509061 20141003 MGI PMID:23028982 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0004043 abnormal pH regulation IAGP N RGD:5509061 20141003 MGI PMID:23028982 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0004287 abnormal spiral limbus morphology IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0004292 abnormal spiral ligament fibrocyte morphology IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0004293 abnormal type I spiral ligament fibrocytes IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0004295 abnormal type III spiral ligament fibrocytes IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0004862 small scala tympani IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0004863 thin spiral ligament IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0005191 head tilt IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0006021 abnormal Reissner membrane morphology IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0006403 abnormal cochlear endolymph ionic homeostasis IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0008309 dilated scala media IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0009349 increased urine pH IAGP N RGD:5509061 20141003 MGI PMID:16174750 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0009349 increased urine pH IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0011417 abnormal renal transport IAGP N RGD:5509061 20141003 MGI PMID:16174750 1321628 Atp6v1b1 ATPase, H+ transporting, lysosomal V1 subunit B1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20171012 MGI PMID:28934385 1321630 Trpm5 transient receptor potential cation channel, subfamily M, member 5 gene MP:0001985 abnormal gustatory system physiology IAGP N RGD:5509061 20141003 MGI PMID:12581520 1321630 Trpm5 transient receptor potential cation channel, subfamily M, member 5 gene MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12581520 1321630 Trpm5 transient receptor potential cation channel, subfamily M, member 5 gene MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16355226 1321630 Trpm5 transient receptor potential cation channel, subfamily M, member 5 gene MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19244541 1321630 Trpm5 transient receptor potential cation channel, subfamily M, member 5 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1321630 Trpm5 transient receptor potential cation channel, subfamily M, member 5 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18758465 1321630 Trpm5 transient receptor potential cation channel, subfamily M, member 5 gene MP:0004209 abnormal sweet taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12581520 1321630 Trpm5 transient receptor potential cation channel, subfamily M, member 5 gene MP:0004209 abnormal sweet taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16355226 1321630 Trpm5 transient receptor potential cation channel, subfamily M, member 5 gene MP:0004210 abnormal bitter taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12581520 1321630 Trpm5 transient receptor potential cation channel, subfamily M, member 5 gene MP:0004210 abnormal bitter taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16355226 1321630 Trpm5 transient receptor potential cation channel, subfamily M, member 5 gene MP:0004211 abnormal sour taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16355226 1321630 Trpm5 transient receptor potential cation channel, subfamily M, member 5 gene MP:0004212 abnormal salty taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16355226 1321630 Trpm5 transient receptor potential cation channel, subfamily M, member 5 gene MP:0004213 abnormal umami taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15738181 1321630 Trpm5 transient receptor potential cation channel, subfamily M, member 5 gene MP:0004213 abnormal umami taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16355226 1321630 Trpm5 transient receptor potential cation channel, subfamily M, member 5 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:18758465 1321632 Sorcs2 sortilin-related VPS10 domain containing receptor 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20150903 MGI PMID:24908487 1321632 Sorcs2 sortilin-related VPS10 domain containing receptor 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20150903 MGI PMID:24908487 1321632 Sorcs2 sortilin-related VPS10 domain containing receptor 2 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20160421 MGI PMID:24908487 1321632 Sorcs2 sortilin-related VPS10 domain containing receptor 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20150903 MGI PMID:24908487 1321632 Sorcs2 sortilin-related VPS10 domain containing receptor 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20150903 MGI PMID:24908487 1321632 Sorcs2 sortilin-related VPS10 domain containing receptor 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20150903 MGI PMID:24908487 1321632 Sorcs2 sortilin-related VPS10 domain containing receptor 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20150903 MGI PMID:24908487 1321632 Sorcs2 sortilin-related VPS10 domain containing receptor 2 gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20150903 MGI PMID:24908487 1321632 Sorcs2 sortilin-related VPS10 domain containing receptor 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:24908487 1321638 Apoh apolipoprotein H gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11145969 1321638 Apoh apolipoprotein H gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11145969 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19016581 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:11051546 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:19940926 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:11051546 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:19940926 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000125 absent incisors IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20151224 MGI PMID:26601902 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19016581 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0001265 decreased body size IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:19016581 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19940926 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20151224 MGI PMID:26601902 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0002083 premature death IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0002238 abnormal nasal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0002388 abnormal Peyer's patch epithelium morphology IAGP N RGD:5509061 20150430 MGI PMID:25751305 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0002388 abnormal Peyer's patch epithelium morphology IAGP N RGD:5509061 20151224 MGI PMID:26601902 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20151224 MGI PMID:26601902 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20151224 MGI PMID:26601902 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0002392 abnormal Peyer's patch T cell area morphology IAGP N RGD:5509061 20151224 MGI PMID:26601902 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:19016581 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:19016581 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:19940926 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20161013 MGI PMID:26659571 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:19016581 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20141003 MGI PMID:19940926 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:17502664 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:19016581 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:19940926 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:19016581 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:11051546 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:15355564 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19940926 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20151224 MGI PMID:26601902 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:10500098 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:19940926 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:19016581 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17502664 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:19940926 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:11051546 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:19016581 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:19016581 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:19016581 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19940926 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0021030 decreased tumor necrosis factor (ligand) superfamily member 11 level IAGP N RGD:5509061 20230202 MGI PMID:33724536 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0021183 increased femoral compact bone area IAGP N RGD:5509061 20220922 MGI PMID:19016581 1321640 Tnfrsf11a tumor necrosis factor receptor superfamily, member 11a, NFKB activator gene MP:0030505 tooth impaction IAGP N RGD:5509061 20191219 MGI PMID:10500098 1321644 Nkx2-9 NK2 homeobox 9 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12571110 1321644 Nkx2-9 NK2 homeobox 9 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:22399681 1321644 Nkx2-9 NK2 homeobox 9 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12571110 1321644 Nkx2-9 NK2 homeobox 9 gene MP:0001075 abnormal accessory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12571110 1321644 Nkx2-9 NK2 homeobox 9 gene MP:0001075 abnormal accessory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:22399681 1321644 Nkx2-9 NK2 homeobox 9 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17079460 1321644 Nkx2-9 NK2 homeobox 9 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:16267219 1321644 Nkx2-9 NK2 homeobox 9 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17079460 1321644 Nkx2-9 NK2 homeobox 9 gene MP:0004568 fusion of glossopharyngeal and vagus nerve IAGP N RGD:5509061 20141003 MGI PMID:12571110 1321644 Nkx2-9 NK2 homeobox 9 gene MP:0004949 absent neuronal precursor cells IAGP N RGD:5509061 20141003 MGI PMID:12571110 1321644 Nkx2-9 NK2 homeobox 9 gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:12571110 1321644 Nkx2-9 NK2 homeobox 9 gene MP:0005488 bronchial epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17079460 1321644 Nkx2-9 NK2 homeobox 9 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17079460 1321644 Nkx2-9 NK2 homeobox 9 gene MP:0010942 abnormal respiratory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17079460 1321644 Nkx2-9 NK2 homeobox 9 gene MP:0010943 abnormal bronchus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17079460 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20181227 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20170119 MGI PMID:27671873 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20181227 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170119 MGI PMID:27671873 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20170119 MGI PMID:27671873 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20181227 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15282322 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:18632607 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15282322 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20170119 MGI PMID:27671873 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18632607 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0002824 abnormal chorioallantoic fusion IEA N RGD:5509061 20181227 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20181227 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18632607 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20170119 MGI PMID:27671873 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20181227 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20181227 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20181227 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20170119 MGI PMID:27671873 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18632607 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20181227 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20170119 MGI PMID:27671873 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:18632607 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15282322 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0011256 abnormal neural fold morphology IAGP N RGD:5509061 20170119 MGI PMID:27671873 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 1321650 Rad9a RAD9 checkpoint clamp component A gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1321652 Upk3a uroplakin 3A gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:11085999 1321652 Upk3a uroplakin 3A gene MP:0001948 vesicoureteral reflux IAGP N RGD:5509061 20141003 MGI PMID:11085999 1321652 Upk3a uroplakin 3A gene MP:0003630 abnormal urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11085999 1321652 Upk3a uroplakin 3A gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:11085999 1321652 Upk3a uroplakin 3A gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:11085999 1321652 Upk3a uroplakin 3A gene MP:0009349 increased urine pH IAGP N RGD:5509061 20141003 MGI PMID:11085999 1321652 Upk3a uroplakin 3A gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:11085999 1321652 Upk3a uroplakin 3A gene MP:0011535 increased urination frequency IAGP N RGD:5509061 20141003 MGI PMID:11085999 1321652 Upk3a uroplakin 3A gene MP:0011783 abnormal ureteral orifice morphology IAGP N RGD:5509061 20141003 MGI PMID:11085999 1321656 Zfp7 zinc finger protein 7 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1321660 Entpd7 ectonucleoside triphosphate diphosphohydrolase 7 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23241884 1321660 Entpd7 ectonucleoside triphosphate diphosphohydrolase 7 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:23241884 1321660 Entpd7 ectonucleoside triphosphate diphosphohydrolase 7 gene MP:0008073 abnormal CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23241884 1321660 Entpd7 ectonucleoside triphosphate diphosphohydrolase 7 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:23241884 1321660 Entpd7 ectonucleoside triphosphate diphosphohydrolase 7 gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:23241884 1321662 Ccna1 cyclin A1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19592082 1321662 Ccna1 cyclin A1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19592082 1321662 Ccna1 cyclin A1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19592082 1321662 Ccna1 cyclin A1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15047941 1321662 Ccna1 cyclin A1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220623 MGI PMID:9843212 1321662 Ccna1 cyclin A1 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:19592082 1321662 Ccna1 cyclin A1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19592082 1321662 Ccna1 cyclin A1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15047941 1321662 Ccna1 cyclin A1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15047941 1321662 Ccna1 cyclin A1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9843212 1321662 Ccna1 cyclin A1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19592082 1321662 Ccna1 cyclin A1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19592082 1321662 Ccna1 cyclin A1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15047941 1321662 Ccna1 cyclin A1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19592082 1321662 Ccna1 cyclin A1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:19592082 1321662 Ccna1 cyclin A1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19592082 1321662 Ccna1 cyclin A1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19592082 1321662 Ccna1 cyclin A1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15047941 1321662 Ccna1 cyclin A1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:9843212 1321662 Ccna1 cyclin A1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:9843212 1321662 Ccna1 cyclin A1 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19592082 1321662 Ccna1 cyclin A1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19592082 1321662 Ccna1 cyclin A1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:9843212 1321662 Ccna1 cyclin A1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:15047941 1321662 Ccna1 cyclin A1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:9843212 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20201029 MGI PMID:32376681 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0001304 cataract IEA N RGD:5509061 20190502 MGI 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20201029 MGI PMID:32376681 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0001925 male infertility IAGP N RGD:5509061 20201029 MGI PMID:32376681 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0001925 male infertility IAGP N RGD:5509061 20220609 MGI PMID:34255152 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20201029 MGI PMID:32376681 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20201029 MGI PMID:32376681 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220609 MGI PMID:34255152 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220609 MGI PMID:34255152 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0002958 cerebral aqueductal stenosis IAGP N RGD:5509061 20201029 MGI PMID:32376681 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20220609 MGI PMID:34255152 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220609 MGI PMID:34255152 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20201029 MGI PMID:32376681 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220609 MGI PMID:34255152 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20201029 MGI PMID:32376681 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220609 MGI PMID:34255152 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220609 MGI PMID:34255152 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220609 MGI PMID:34255152 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20220609 MGI PMID:34255152 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220609 MGI PMID:34255152 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20201029 MGI PMID:32376681 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20201029 MGI PMID:32376681 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20201029 MGI PMID:32376681 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0013228 brain ventricle stenosis IAGP N RGD:5509061 20201029 MGI PMID:32376681 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220609 MGI PMID:34255152 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0030316 enlarged neurocranium IAGP N RGD:5509061 20201029 MGI PMID:32376681 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20220609 MGI PMID:34255152 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220609 MGI PMID:34255152 1321666 Cfap206 cilia and flagella associated protein 206 gene MP:0031438 abnormal sperm radial spoke morphology IAGP N RGD:5509061 20220915 MGI PMID:32376681 1321671 Cul2 cullin 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321671 Cul2 cullin 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20230914 MGI PMID:37233188 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0002083 premature death IAGP N RGD:5509061 20230914 MGI PMID:37233188 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20230914 MGI PMID:37233188 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20230914 MGI PMID:37233188 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20230914 MGI PMID:37233188 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20230914 MGI PMID:37233188 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20230914 MGI PMID:37233188 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20230914 MGI PMID:37233188 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20230914 MGI PMID:37233188 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20230914 MGI PMID:37233188 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20230914 MGI PMID:37233188 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20230914 MGI PMID:37233188 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0021160 decreased heart right ventricle wall thickness IAGP N RGD:5509061 20230914 MGI PMID:37233188 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20230914 MGI PMID:37233188 1321685 Rtf1 RTF1, Paf1/RNA polymerase II complex component gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:37233188 1321691 Kctd3 potassium channel tetramerisation domain containing 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210826 MGI 1321691 Kctd3 potassium channel tetramerisation domain containing 3 gene MP:0001785 edema IEA N RGD:5509061 20210826 MGI 1321691 Kctd3 potassium channel tetramerisation domain containing 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220519 MGI 1321691 Kctd3 potassium channel tetramerisation domain containing 3 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 1321691 Kctd3 potassium channel tetramerisation domain containing 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1321691 Kctd3 potassium channel tetramerisation domain containing 3 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1321694 Ppdpf pancreatic progenitor cell differentiation and proliferation factor gene MP:0001260 increased body weight IAGP N RGD:5509061 20210826 MGI PMID:34031390 1321694 Ppdpf pancreatic progenitor cell differentiation and proliferation factor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20210826 MGI PMID:34031390 1321694 Ppdpf pancreatic progenitor cell differentiation and proliferation factor gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20210826 MGI PMID:34031390 1321694 Ppdpf pancreatic progenitor cell differentiation and proliferation factor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20210826 MGI PMID:34031390 1321694 Ppdpf pancreatic progenitor cell differentiation and proliferation factor gene MP:0002981 increased liver weight IAGP N RGD:5509061 20210826 MGI PMID:34031390 1321694 Ppdpf pancreatic progenitor cell differentiation and proliferation factor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210826 MGI PMID:34031390 1321694 Ppdpf pancreatic progenitor cell differentiation and proliferation factor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20210826 MGI PMID:34031390 1321694 Ppdpf pancreatic progenitor cell differentiation and proliferation factor gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20210826 MGI PMID:34031390 1321694 Ppdpf pancreatic progenitor cell differentiation and proliferation factor gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1321694 Ppdpf pancreatic progenitor cell differentiation and proliferation factor gene MP:0020867 increased lipogenesis IAGP N RGD:5509061 20210826 MGI PMID:34031390 1321694 Ppdpf pancreatic progenitor cell differentiation and proliferation factor gene MP:0031269 increased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210826 MGI PMID:34031390 1321700 Tpr translocated promoter region, nuclear basket protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321707 Afap1l2 actin filament associated protein 1-like 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1321707 Afap1l2 actin filament associated protein 1-like 2 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20230601 MGI 1321707 Afap1l2 actin filament associated protein 1-like 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 1321707 Afap1l2 actin filament associated protein 1-like 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1321707 Afap1l2 actin filament associated protein 1-like 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1321707 Afap1l2 actin filament associated protein 1-like 2 gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20200102 MGI PMID:25272040 1321707 Afap1l2 actin filament associated protein 1-like 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1321707 Afap1l2 actin filament associated protein 1-like 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1321707 Afap1l2 actin filament associated protein 1-like 2 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20200102 MGI PMID:25272040 1321707 Afap1l2 actin filament associated protein 1-like 2 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20150430 MGI 1321707 Afap1l2 actin filament associated protein 1-like 2 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210826 MGI 1321707 Afap1l2 actin filament associated protein 1-like 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20150430 MGI 1321707 Afap1l2 actin filament associated protein 1-like 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20200402 MGI 1321707 Afap1l2 actin filament associated protein 1-like 2 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1321709 Iqch IQ motif containing H gene MP:0001147 small testis IAGP N RGD:5509061 20240425 MGI PMID:36975404 1321709 Iqch IQ motif containing H gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1321709 Iqch IQ motif containing H gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1321709 Iqch IQ motif containing H gene MP:0001925 male infertility IAGP N RGD:5509061 20240425 MGI PMID:36975404 1321709 Iqch IQ motif containing H gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20240425 MGI PMID:36975404 1321709 Iqch IQ motif containing H gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240425 MGI PMID:36975404 1321709 Iqch IQ motif containing H gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240425 MGI PMID:36975404 1321709 Iqch IQ motif containing H gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20240425 MGI PMID:36975404 1321709 Iqch IQ motif containing H gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20240425 MGI PMID:36975404 1321709 Iqch IQ motif containing H gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20240425 MGI PMID:36975404 1321709 Iqch IQ motif containing H gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20240425 MGI PMID:36975404 1321709 Iqch IQ motif containing H gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240425 MGI PMID:36975404 1321709 Iqch IQ motif containing H gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20240425 MGI PMID:36975404 1321709 Iqch IQ motif containing H gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1321711 Rmi1 RecQ mediated genome instability 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20050919 1321711 Rmi1 RecQ mediated genome instability 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:20050919 1321711 Rmi1 RecQ mediated genome instability 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20050919 1321711 Rmi1 RecQ mediated genome instability 1 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20050919 1321711 Rmi1 RecQ mediated genome instability 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20050919 1321711 Rmi1 RecQ mediated genome instability 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20050919 1321711 Rmi1 RecQ mediated genome instability 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:20050919 1321711 Rmi1 RecQ mediated genome instability 1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:20050919 1321711 Rmi1 RecQ mediated genome instability 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20050919 1321711 Rmi1 RecQ mediated genome instability 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:20050919 1321713 Arhgef3 Rho guanine nucleotide exchange factor 3 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20170720 MGI PMID:28542600 1321713 Arhgef3 Rho guanine nucleotide exchange factor 3 gene MP:0005397 hematopoietic system phenotype IAGP N RGD:5509061 20201231 MGI PMID:28542600 1321713 Arhgef3 Rho guanine nucleotide exchange factor 3 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20170720 MGI PMID:28542600 1321713 Arhgef3 Rho guanine nucleotide exchange factor 3 gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20210610 MGI PMID:33406419 1321713 Arhgef3 Rho guanine nucleotide exchange factor 3 gene MP:0013161 enhanced muscle regeneration IAGP N RGD:5509061 20210610 MGI PMID:33406419 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:17936561 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:22674806 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:17936561 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20170209 MGI PMID:17936561 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20170209 MGI PMID:7621074 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170209 MGI PMID:17936561 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170209 MGI PMID:22674806 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230119 MGI 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230119 MGI 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170209 MGI PMID:7621074 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0001577 anemia IAGP N RGD:5509061 20170209 MGI PMID:22674806 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20170209 MGI PMID:7621074 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:7621074 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20170209 MGI PMID:22674806 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20170209 MGI PMID:24440599 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20170209 MGI PMID:22674806 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20170209 MGI PMID:24440599 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20170209 MGI PMID:17936561 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:15951813 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:17936561 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:7621074 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20170209 MGI PMID:17936561 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20170209 MGI PMID:7621074 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20170209 MGI PMID:16688530 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20170209 MGI PMID:22674806 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230119 MGI 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:7621074 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170209 MGI PMID:17936561 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170209 MGI PMID:7621074 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20170209 MGI PMID:17936561 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20170209 MGI PMID:7621074 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20170209 MGI PMID:7621074 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20170209 MGI PMID:7621074 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20170209 MGI PMID:17936561 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20170209 MGI PMID:7621074 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20170209 MGI PMID:7621074 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20170209 MGI PMID:7621074 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20170209 MGI PMID:17936561 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20170209 MGI PMID:7621074 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20170209 MGI PMID:18245664 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20170209 MGI PMID:17936561 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20170209 MGI PMID:17936561 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008618 decreased circulating interleukin-12 level IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0009709 hydrometra IEA N RGD:5509061 20230119 MGI 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20170209 MGI PMID:20457904 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20170209 MGI PMID:22674806 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0011815 increased pre-pro B cell number IAGP N RGD:5509061 20170209 MGI PMID:24255108 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0013771 decreased effector memory T-helper cell number IEA N RGD:5509061 20230119 MGI 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:16688530 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:16688530 1321715 Flt3 FMS-like tyrosine kinase 3 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:20457904 1321716 Smpd4 sphingomyelin phosphodiesterase 4 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1321716 Smpd4 sphingomyelin phosphodiesterase 4 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20170504 MGI 1321716 Smpd4 sphingomyelin phosphodiesterase 4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170504 MGI 1321716 Smpd4 sphingomyelin phosphodiesterase 4 gene MP:0003586 dilated ureter IEA N RGD:5509061 20170504 MGI 1321716 Smpd4 sphingomyelin phosphodiesterase 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1321716 Smpd4 sphingomyelin phosphodiesterase 4 gene MP:0011513 abnormal vertebral artery morphology IEA N RGD:5509061 20170504 MGI 1321717 Ropn1 ropporin, rhophilin associated protein 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:22021175 1321717 Ropn1 ropporin, rhophilin associated protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22021175 1321717 Ropn1 ropporin, rhophilin associated protein 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:22021175 1321717 Ropn1 ropporin, rhophilin associated protein 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22021175 1321717 Ropn1 ropporin, rhophilin associated protein 1 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220714 MGI PMID:22021175 1321721 Cldn15 claudin 15 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18242218 1321721 Cldn15 claudin 15 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18242218 1321721 Cldn15 claudin 15 gene MP:0000481 abnormal enterocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18242218 1321721 Cldn15 claudin 15 gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20141003 MGI PMID:18242218 1321721 Cldn15 claudin 15 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18242218 1321721 Cldn15 claudin 15 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:18242218 1321721 Cldn15 claudin 15 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18242218 1321721 Cldn15 claudin 15 gene MP:0009483 enlarged ileum IAGP N RGD:5509061 20141003 MGI PMID:18242218 1321721 Cldn15 claudin 15 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20150618 MGI PMID:18242218 1321721 Cldn15 claudin 15 gene MP:0011882 enlarged duodenum IAGP N RGD:5509061 20150618 MGI PMID:18242218 1321721 Cldn15 claudin 15 gene MP:0013796 abnormal duodenal goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:18242218 1321721 Cldn15 claudin 15 gene MP:0013798 abnormal jeujunal goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:18242218 1321723 Foxs1 forkhead box S1 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:15964817 1321723 Foxs1 forkhead box S1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15964817 1321723 Foxs1 forkhead box S1 gene MP:0009489 abnormal blood vessel endothelium morphology IAGP N RGD:5509061 20201015 MGI PMID:18288644 1321723 Foxs1 forkhead box S1 gene MP:0031138 testicular hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:18288644 1321724 Tmem151a transmembrane protein 151A gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20240912 MGI PMID:34518509 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0000160 kyphosis IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0001263 weight loss IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0001513 limb grasping IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0002083 premature death IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0002183 gliosis IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0008291 abnormal adrenocortical cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0008579 abnormal Purkinje cell differentiation IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0012217 increased plasmalogen level IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0012218 decreased brain plasmalogen level IAGP N RGD:5509061 20150528 MGI PMID:20959636 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0014010 abnormal peroxisome morphology IAGP N RGD:5509061 20230615 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0020847 abnormal peroxisome physiology IAGP N RGD:5509061 20230615 MGI PMID:12897163 1321727 Pex13 peroxisomal biogenesis factor 13 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:12897163 1321728 Ccnyl1 cyclin Y-like 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20151008 MGI PMID:26305884 1321728 Ccnyl1 cyclin Y-like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20151008 MGI PMID:26305884 1321728 Ccnyl1 cyclin Y-like 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20151008 MGI PMID:26305884 1321728 Ccnyl1 cyclin Y-like 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20151008 MGI PMID:26305884 1321728 Ccnyl1 cyclin Y-like 1 gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20151008 MGI PMID:26305884 1321728 Ccnyl1 cyclin Y-like 1 gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20151008 MGI PMID:26305884 1321728 Ccnyl1 cyclin Y-like 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20151008 MGI PMID:26305884 1321728 Ccnyl1 cyclin Y-like 1 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220714 MGI PMID:26305884 1321730 Immt inner membrane protein, mitochondrial gene MP:0000852 small cerebellum IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0001405 impaired coordination IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0001406 abnormal gait IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0001407 short stride length IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0002879 increased cellular sensitivity to X-ray irradiation IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0003214 neurofibrillary tangles IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0003674 oxidative stress IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0003927 increased cellular glucose import IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0011637 abnormal mitochondrial matrix morphology IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0013243 abnormal carbohydrate metabolism IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0014342 abnormal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0014345 abnormal neuron mitochondrial morphology IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321730 Immt inner membrane protein, mitochondrial gene MP:0020083 decreased hippocampus volume IAGP N RGD:5509061 20240222 MGI PMID:36974636 1321733 Cdip1 cell death inducing Trp53 target 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1321733 Cdip1 cell death inducing Trp53 target 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20181227 MGI 1321733 Cdip1 cell death inducing Trp53 target 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20190418 MGI PMID:24139803 1321733 Cdip1 cell death inducing Trp53 target 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321733 Cdip1 cell death inducing Trp53 target 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1321735 Elf3 E74-like factor 3 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11984530 1321735 Elf3 E74-like factor 3 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11984530 1321735 Elf3 E74-like factor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11984530 1321735 Elf3 E74-like factor 3 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11984530 1321735 Elf3 E74-like factor 3 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:11984530 1321735 Elf3 E74-like factor 3 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:11984530 1321735 Elf3 E74-like factor 3 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:11984530 1321735 Elf3 E74-like factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11984530 1321735 Elf3 E74-like factor 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11984530 1321735 Elf3 E74-like factor 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:12808099 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:12808099 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16525419 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18093944 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18093944 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18093944 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:12808099 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0001876 decreased inflammatory response IEA N RGD:5509061 20220811 MGI 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12808099 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12808099 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12808099 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12808099 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12808099 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:18093944 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:16525419 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:18093944 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0003880 abnormal central pattern generator function IAGP N RGD:5509061 20141003 MGI PMID:18093944 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0004557 dilated allantois IAGP N RGD:5509061 20141003 MGI PMID:12808099 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0004712 notochord degeneration IAGP N RGD:5509061 20141003 MGI PMID:12808099 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16525419 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16525419 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16525419 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12808099 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:16525419 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:16525419 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0008503 abnormal spinal cord grey matter morphology IAGP N RGD:5509061 20141003 MGI PMID:18093944 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12808099 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:18093944 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18093944 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808099 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:16525419 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0011856 abnormal glomerular filtration barrier function IAGP N RGD:5509061 20141003 MGI PMID:16525419 1321737 Nck1 non-catalytic region of tyrosine kinase adaptor protein 1 gene MP:0020100 decreased susceptibility to diet-induced aortic fatty streak lesions IEA N RGD:5509061 20220811 MGI 1321739 Msh6 mutS homolog 6 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15324697 1321739 Msh6 mutS homolog 6 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9390556 1321739 Msh6 mutS homolog 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10706084 1321739 Msh6 mutS homolog 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9390556 1321739 Msh6 mutS homolog 6 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15324697 1321739 Msh6 mutS homolog 6 gene MP:0002492 decreased IgE level IEA N RGD:5509061 20180215 MGI 1321739 Msh6 mutS homolog 6 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10706084 1321739 Msh6 mutS homolog 6 gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15324697 1321739 Msh6 mutS homolog 6 gene MP:0009222 increased uterus tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10545954 1321739 Msh6 mutS homolog 6 gene MP:0009797 abnormal mismatch repair IAGP N RGD:5509061 20141003 MGI PMID:10706084 1321739 Msh6 mutS homolog 6 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10545954 1321739 Msh6 mutS homolog 6 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10706084 1321739 Msh6 mutS homolog 6 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9390556 1321739 Msh6 mutS homolog 6 gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10545954 1321739 Msh6 mutS homolog 6 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10545954 1321739 Msh6 mutS homolog 6 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10545954 1321739 Msh6 mutS homolog 6 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10706084 1321739 Msh6 mutS homolog 6 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15324697 1321739 Msh6 mutS homolog 6 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9390556 1321739 Msh6 mutS homolog 6 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:10545954 1321739 Msh6 mutS homolog 6 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:15324697 1321741 U2af2 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20220519 MGI 1321741 U2af2 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20230601 MGI 1321741 U2af2 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240926 MGI 1321741 U2af2 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240523 MGI 1321741 U2af2 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20230601 MGI 1321741 U2af2 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241017 MGI 1321741 U2af2 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1321741 U2af2 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1321744 Galnt2 polypeptide N-acetylgalactosaminyltransferase 2 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20191114 MGI PMID:27508872 1321744 Galnt2 polypeptide N-acetylgalactosaminyltransferase 2 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20191114 MGI PMID:27508872 1321744 Galnt2 polypeptide N-acetylgalactosaminyltransferase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1321744 Galnt2 polypeptide N-acetylgalactosaminyltransferase 2 gene MP:0011582 decreased triglyceride lipase activity IAGP N RGD:5509061 20191114 MGI PMID:27508872 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0000434 megacephaly IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0000440 domed cranium IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0000747 muscle weakness IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0001872 sinus inflammation IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20221215 MGI 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0003354 astrocytosis IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0004924 abnormal behavior IEA N RGD:5509061 20221215 MGI 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0005202 lethargy IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0005238 increased brain size IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0008918 microgliosis IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20160421 MGI 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0013907 abnormal cerebrospinal fluid flow IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321746 Rsph9 radial spoke head 9 homolog (Chlamydomonas) gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20201029 MGI PMID:32709945 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:3860691 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:3860691 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20736371 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:3860691 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20736371 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:3860691 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20736371 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:3860691 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20151126 MGI PMID:23773267 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201022 MGI 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20211021 MGI 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0004478 increased testicular teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:3860691 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0004478 increased testicular teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:4692863 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:3860691 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20151126 MGI PMID:23773267 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:3860691 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:3860691 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20151126 MGI PMID:23773267 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:3860691 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20736371 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:3860691 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20151126 MGI PMID:23773267 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20211021 MGI 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20151126 MGI PMID:23773267 1321749 Dnd1 DND microRNA-mediated repression inhibitor 1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20151126 MGI PMID:23773267 1321753 Cwc27 CWC27 spliceosome-associated protein gene MP:0001732 postnatal growth retardation IEA N RGD:5509061 20170413 MGI 1321753 Cwc27 CWC27 spliceosome-associated protein gene MP:0001790 abnormal immune system physiology IEA N RGD:5509061 20170413 MGI 1321753 Cwc27 CWC27 spliceosome-associated protein gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1321753 Cwc27 CWC27 spliceosome-associated protein gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20190822 MGI PMID:28285769 1321753 Cwc27 CWC27 spliceosome-associated protein gene MP:0004924 abnormal behavior IEA N RGD:5509061 20170413 MGI 1321753 Cwc27 CWC27 spliceosome-associated protein gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20190822 MGI PMID:28285769 1321753 Cwc27 CWC27 spliceosome-associated protein gene MP:0009642 abnormal blood homeostasis IEA N RGD:5509061 20170413 MGI 1321753 Cwc27 CWC27 spliceosome-associated protein gene MP:0010865 prenatal growth retardation IEA N RGD:5509061 20170413 MGI 1321753 Cwc27 CWC27 spliceosome-associated protein gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20160421 MGI 1321753 Cwc27 CWC27 spliceosome-associated protein gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20190822 MGI PMID:28285769 1321753 Cwc27 CWC27 spliceosome-associated protein gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20190822 MGI PMID:28285769 1321753 Cwc27 CWC27 spliceosome-associated protein gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20190822 MGI PMID:28285769 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20170202 MGI PMID:26494538 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26494538 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0004035 abnormal sublingual gland morphology IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20170202 MGI PMID:26494538 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0009149 decreased pancreatic acinar cell number IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0009154 pancreatic acinar hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0009162 absent pancreatic acinar cell zymogen granule IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0009165 abnormal endocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0010148 abnormal exocrine pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170202 MGI PMID:26494538 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0011932 abnormal endocrine pancreas development IAGP N RGD:5509061 20141003 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0013568 gastric gland degeneration IAGP N RGD:5509061 20150305 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0013581 nasal gland degeneration IAGP N RGD:5509061 20150305 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0013583 salivary gland degeneration IAGP N RGD:5509061 20150312 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0013584 pancreas degeneration IAGP N RGD:5509061 20150312 MGI PMID:22745161 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:26494538 1321757 Sec23b SEC23 homolog B, COPII coat complex component gene MP:0014260 embryonic lethality prior to organogenesis, incomplete penetrance IAGP N RGD:5509061 20230706 MGI PMID:26494538 1321759 Alg1 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1321759 Alg1 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20170105 MGI 1321759 Alg1 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1321759 Alg1 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1321759 Alg1 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1321759 Alg1 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20211021 MGI 1321759 Alg1 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321761 Kdm1b lysine (K)-specific demethylase 1B gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19727073 1321761 Kdm1b lysine (K)-specific demethylase 1B gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:19727073 1321767 Gpank1 G patch domain and ankyrin repeats 1 gene MP:0005575 increased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 1321767 Gpank1 G patch domain and ankyrin repeats 1 gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20210128 MGI 1321767 Gpank1 G patch domain and ankyrin repeats 1 gene MP:0005585 increased tidal volume IEA N RGD:5509061 20201022 MGI 1321770 Cic capicua transcriptional repressor gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20190215 MGI PMID:28288114 1321770 Cic capicua transcriptional repressor gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20201002 MGI PMID:32229723 1321770 Cic capicua transcriptional repressor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22014525 1321770 Cic capicua transcriptional repressor gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20190215 MGI PMID:28288114 1321770 Cic capicua transcriptional repressor gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20190215 MGI PMID:28288114 1321770 Cic capicua transcriptional repressor gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20190215 MGI PMID:28288114 1321770 Cic capicua transcriptional repressor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20190215 MGI PMID:28288114 1321770 Cic capicua transcriptional repressor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20201002 MGI PMID:32229723 1321770 Cic capicua transcriptional repressor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22053053 1321770 Cic capicua transcriptional repressor gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20201002 MGI PMID:32229723 1321770 Cic capicua transcriptional repressor gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:22014525 1321770 Cic capicua transcriptional repressor gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20190215 MGI PMID:28288114 1321770 Cic capicua transcriptional repressor gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:22053053 1321770 Cic capicua transcriptional repressor gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20190215 MGI PMID:28288114 1321770 Cic capicua transcriptional repressor gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20201002 MGI PMID:32229723 1321770 Cic capicua transcriptional repressor gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20190215 MGI PMID:28288114 1321770 Cic capicua transcriptional repressor gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20201002 MGI PMID:32229723 1321770 Cic capicua transcriptional repressor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22014525 1321770 Cic capicua transcriptional repressor gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20201002 MGI PMID:32229723 1321770 Cic capicua transcriptional repressor gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20190215 MGI PMID:28288114 1321770 Cic capicua transcriptional repressor gene MP:0020337 abnormal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20190215 MGI PMID:28288114 1321770 Cic capicua transcriptional repressor gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20190215 MGI PMID:28288114 1321770 Cic capicua transcriptional repressor gene MP:0020594 decreased cerebral cortex cell number IAGP N RGD:5509061 20190215 MGI PMID:28288114 1321770 Cic capicua transcriptional repressor gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:28288114 1321772 Diaph1 diaphanous related formin 1 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0000256 echinocytosis IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141225 MGI PMID:22246438 1321772 Diaph1 diaphanous related formin 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141225 MGI PMID:22246438 1321772 Diaph1 diaphanous related formin 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141225 MGI PMID:22246438 1321772 Diaph1 diaphanous related formin 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17682067 1321772 Diaph1 diaphanous related formin 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0002492 decreased IgE level IEA N RGD:5509061 20180215 MGI 1321772 Diaph1 diaphanous related formin 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141225 MGI PMID:22246438 1321772 Diaph1 diaphanous related formin 1 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:17682067 1321772 Diaph1 diaphanous related formin 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0004978 decreased B-1 B cell number IEA N RGD:5509061 20180215 MGI 1321772 Diaph1 diaphanous related formin 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17682067 1321772 Diaph1 diaphanous related formin 1 gene MP:0005046 absent spleen white pulp IAGP N RGD:5509061 20141003 MGI PMID:17699759 1321772 Diaph1 diaphanous related formin 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17682067 1321772 Diaph1 diaphanous related formin 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20230601 MGI 1321772 Diaph1 diaphanous related formin 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141225 MGI PMID:22246438 1321772 Diaph1 diaphanous related formin 1 gene MP:0008073 abnormal CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1321772 Diaph1 diaphanous related formin 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17682067 1321772 Diaph1 diaphanous related formin 1 gene MP:0008077 abnormal CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1321772 Diaph1 diaphanous related formin 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17682067 1321772 Diaph1 diaphanous related formin 1 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17682067 1321772 Diaph1 diaphanous related formin 1 gene MP:0009949 abnormal olfactory bulb granule cell layer morphology IAGP N RGD:5509061 20141225 MGI PMID:22246438 1321772 Diaph1 diaphanous related formin 1 gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20180215 MGI 1321772 Diaph1 diaphanous related formin 1 gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20180215 MGI 1321772 Diaph1 diaphanous related formin 1 gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20180215 MGI 1321772 Diaph1 diaphanous related formin 1 gene MP:0010839 decreased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20180215 MGI 1321772 Diaph1 diaphanous related formin 1 gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1321772 Diaph1 diaphanous related formin 1 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1321772 Diaph1 diaphanous related formin 1 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1321772 Diaph1 diaphanous related formin 1 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1321772 Diaph1 diaphanous related formin 1 gene MP:0010851 decreased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1321772 Diaph1 diaphanous related formin 1 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1321772 Diaph1 diaphanous related formin 1 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IEA N RGD:5509061 20200514 MGI 1321776 Ccdc77 coiled-coil domain containing 77 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20211021 MGI 1321778 Acap3 ArfGAP with coiled-coil, ankyrin repeat and PH domains 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20141003 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0001148 enlarged testis IEA N RGD:5509061 20230601 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20230601 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20230601 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0002764 short tibia IEA N RGD:5509061 20230601 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0003036 vertebral transformation IEA N RGD:5509061 20230601 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0003917 increased kidney weight IEA N RGD:5509061 20240523 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20230601 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230601 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0008044 increased NK cell number IEA N RGD:5509061 20230601 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230601 MGI 1321779 Emsy EMSY, BRCA2-interacting transcriptional repressor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1321783 Cbx1 chromobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12904583 1321783 Cbx1 chromobox 1 gene MP:0008762 embryonic lethality IEA N RGD:5509061 20141003 MGI 1321783 Cbx1 chromobox 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20221215 MGI 1321785 Sytl1 synaptotagmin-like 1 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20160922 MGI PMID:24652767 1321785 Sytl1 synaptotagmin-like 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20160804 MGI 1321785 Sytl1 synaptotagmin-like 1 gene MP:0002694 abnormal pancreas secretion IAGP N RGD:5509061 20141003 MGI PMID:18477466 1321785 Sytl1 synaptotagmin-like 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20160804 MGI 1321785 Sytl1 synaptotagmin-like 1 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20160922 MGI PMID:24652767 1321785 Sytl1 synaptotagmin-like 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:23223571 1321785 Sytl1 synaptotagmin-like 1 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20160922 MGI PMID:24652767 1321785 Sytl1 synaptotagmin-like 1 gene MP:0003596 epididymis inflammation IAGP N RGD:5509061 20160922 MGI PMID:24652767 1321785 Sytl1 synaptotagmin-like 1 gene MP:0004614 caudal vertebral transformation IAGP N RGD:5509061 20160922 MGI PMID:24652767 1321785 Sytl1 synaptotagmin-like 1 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1321785 Sytl1 synaptotagmin-like 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1321785 Sytl1 synaptotagmin-like 1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23223571 1321785 Sytl1 synaptotagmin-like 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1321785 Sytl1 synaptotagmin-like 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1321785 Sytl1 synaptotagmin-like 1 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1321785 Sytl1 synaptotagmin-like 1 gene MP:0008805 decreased circulating amylase level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1321785 Sytl1 synaptotagmin-like 1 gene MP:0009161 pancreatic acinar cell zymogen granule accumulation IAGP N RGD:5509061 20141003 MGI PMID:18477466 1321785 Sytl1 synaptotagmin-like 1 gene MP:0031110 meningitis IAGP N RGD:5509061 20200910 MGI PMID:24652767 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0000160 kyphosis IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0000746 weakness IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0000754 paresis IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20200310 MGI PMID:16551741 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20200310 MGI PMID:17549747 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20200310 MGI PMID:17549747 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:16551741 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:16551741 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20231214 MGI PMID:37862170 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:16551741 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0001525 impaired balance IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20200310 MGI PMID:18941222 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18941222 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20200310 MGI PMID:18941222 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20200310 MGI PMID:17549747 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20200310 MGI PMID:18941222 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20231214 MGI PMID:37862170 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20200310 MGI PMID:20937851 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20240613 MGI PMID:35663027 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20231214 MGI PMID:37862170 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0009080 uterus inflammation IAGP N RGD:5509061 20240613 MGI PMID:35663027 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20240613 MGI PMID:35663027 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11395000 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20231214 MGI PMID:37862170 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:16551741 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:17549747 1321787 Ccr10 C-C motif chemokine receptor 10 gene MP:0020212 impaired leukocyte migration IAGP N RGD:5509061 20240613 MGI PMID:35663027 1321792 Klra17 killer cell lectin-like receptor, subfamily A, member 17 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:19075287 1321792 Klra17 killer cell lectin-like receptor, subfamily A, member 17 gene MP:0008524 increased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:19075287 1321792 Klra17 killer cell lectin-like receptor, subfamily A, member 17 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:19075287 1321792 Klra17 killer cell lectin-like receptor, subfamily A, member 17 gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:19075287 1321792 Klra17 killer cell lectin-like receptor, subfamily A, member 17 gene MP:0008618 decreased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:19075287 1321792 Klra17 killer cell lectin-like receptor, subfamily A, member 17 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:19075287 1321792 Klra17 killer cell lectin-like receptor, subfamily A, member 17 gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19075287 1321792 Klra17 killer cell lectin-like receptor, subfamily A, member 17 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:19075287 1321794 Fmc1 formation of mitochondrial complex V assembly factor 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1321794 Fmc1 formation of mitochondrial complex V assembly factor 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20201231 MGI 1321794 Fmc1 formation of mitochondrial complex V assembly factor 1 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20190502 MGI 1321794 Fmc1 formation of mitochondrial complex V assembly factor 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 1321794 Fmc1 formation of mitochondrial complex V assembly factor 1 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20200310 MGI PMID:29371327 1321794 Fmc1 formation of mitochondrial complex V assembly factor 1 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:29371327 1321794 Fmc1 formation of mitochondrial complex V assembly factor 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20200310 MGI PMID:29371327 1321794 Fmc1 formation of mitochondrial complex V assembly factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29371327 1321794 Fmc1 formation of mitochondrial complex V assembly factor 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29371327 1321794 Fmc1 formation of mitochondrial complex V assembly factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241003 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230601 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0002718 abnormal inner cell mass morphology IEA N RGD:5509061 20241003 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IEA N RGD:5509061 20241017 MGI 1321796 Dhx8 DEAH-box helicase 8 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1321806 Rbm14 RNA binding motif protein 14 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1321806 Rbm14 RNA binding motif protein 14 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20201001 MGI PMID:31794640 1321806 Rbm14 RNA binding motif protein 14 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20201001 MGI PMID:31794640 1321806 Rbm14 RNA binding motif protein 14 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20201001 MGI PMID:31794640 1321806 Rbm14 RNA binding motif protein 14 gene MP:0003087 absent allantois IAGP N RGD:5509061 20201001 MGI PMID:31794640 1321806 Rbm14 RNA binding motif protein 14 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20201001 MGI PMID:31794640 1321806 Rbm14 RNA binding motif protein 14 gene MP:0005030 absent amnion IAGP N RGD:5509061 20201001 MGI PMID:31794640 1321806 Rbm14 RNA binding motif protein 14 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1321806 Rbm14 RNA binding motif protein 14 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20201001 MGI PMID:31794640 1321806 Rbm14 RNA binding motif protein 14 gene MP:0006323 abnormal extraembryonic mesoderm development IAGP N RGD:5509061 20201001 MGI PMID:31794640 1321806 Rbm14 RNA binding motif protein 14 gene MP:0009593 absent chorion IAGP N RGD:5509061 20201001 MGI PMID:31794640 1321806 Rbm14 RNA binding motif protein 14 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20201001 MGI PMID:31794640 1321806 Rbm14 RNA binding motif protein 14 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20201001 MGI PMID:31794640 1321809 Mlph melanophilin gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:11504925 1321809 Mlph melanophilin gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:17247639 1321809 Mlph melanophilin gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:3410303 1321809 Mlph melanophilin gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:5713933 1321809 Mlph melanophilin gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:5726144 1321809 Mlph melanophilin gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17247639 1321809 Mlph melanophilin gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:5726144 1321809 Mlph melanophilin gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:5726144 1321809 Mlph melanophilin gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17247639 1321809 Mlph melanophilin gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:6696991 1321809 Mlph melanophilin gene MP:0008733 abnormal hair shaft melanin granule distribution IAGP N RGD:5509061 20141003 MGI PMID:17247639 1321809 Mlph melanophilin gene MP:0009555 abnormal hair follicle melanin granule distribution IAGP N RGD:5509061 20141003 MGI PMID:4634048 1321809 Mlph melanophilin gene MP:0010193 abnormal choroid melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 1321811 Pla2g7 phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma) gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20211021 MGI 1321811 Pla2g7 phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma) gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20160225 MGI PMID:20531249 1321811 Pla2g7 phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma) gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1321811 Pla2g7 phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma) gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1321811 Pla2g7 phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma) gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20240523 MGI 1321811 Pla2g7 phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma) gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20170622 MGI PMID:20531249 1321813 Trmt10b tRNA methyltransferase 10B gene MP:0001284 absent vibrissae IEA N RGD:5509061 20220811 MGI 1321813 Trmt10b tRNA methyltransferase 10B gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1321813 Trmt10b tRNA methyltransferase 10B gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1321820 Lipg lipase, endothelial gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15304490 1321820 Lipg lipase, endothelial gene MP:0000184 abnormal circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17681148 1321820 Lipg lipase, endothelial gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12569160 1321820 Lipg lipase, endothelial gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15304490 1321820 Lipg lipase, endothelial gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12569160 1321820 Lipg lipase, endothelial gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12601178 1321820 Lipg lipase, endothelial gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15304490 1321820 Lipg lipase, endothelial gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:12569160 1321820 Lipg lipase, endothelial gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:12601178 1321820 Lipg lipase, endothelial gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:15304490 1321820 Lipg lipase, endothelial gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15485805 1321820 Lipg lipase, endothelial gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15304490 1321820 Lipg lipase, endothelial gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12569160 1321820 Lipg lipase, endothelial gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12601178 1321820 Lipg lipase, endothelial gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15304490 1321820 Lipg lipase, endothelial gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12601178 1321820 Lipg lipase, endothelial gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15304490 1321820 Lipg lipase, endothelial gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15304490 1321822 Zswim5 zinc finger SWIM-type containing 5 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160114 MGI 1321824 Dact2 dishevelled-binding antagonist of beta-catenin 2 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20190502 MGI 1321824 Dact2 dishevelled-binding antagonist of beta-catenin 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1321824 Dact2 dishevelled-binding antagonist of beta-catenin 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20190502 MGI 1321824 Dact2 dishevelled-binding antagonist of beta-catenin 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1321824 Dact2 dishevelled-binding antagonist of beta-catenin 2 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:18716284 1321824 Dact2 dishevelled-binding antagonist of beta-catenin 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1321824 Dact2 dishevelled-binding antagonist of beta-catenin 2 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1321824 Dact2 dishevelled-binding antagonist of beta-catenin 2 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 1321824 Dact2 dishevelled-binding antagonist of beta-catenin 2 gene MP:0012193 increased keratinocyte migration IAGP N RGD:5509061 20141204 MGI PMID:18716284 1321828 Stag1 STAG1 cohesin complex component gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:22415368 1321828 Stag1 STAG1 cohesin complex component gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:22415368 1321828 Stag1 STAG1 cohesin complex component gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220811 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:22415368 1321828 Stag1 STAG1 cohesin complex component gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20220811 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210520 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22415368 1321828 Stag1 STAG1 cohesin complex component gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22415368 1321828 Stag1 STAG1 cohesin complex component gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22415368 1321828 Stag1 STAG1 cohesin complex component gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20220811 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:22415368 1321828 Stag1 STAG1 cohesin complex component gene MP:0002989 small kidney IEA N RGD:5509061 20210128 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20221215 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210520 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22415368 1321828 Stag1 STAG1 cohesin complex component gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:22415368 1321828 Stag1 STAG1 cohesin complex component gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:22415368 1321828 Stag1 STAG1 cohesin complex component gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:22415368 1321828 Stag1 STAG1 cohesin complex component gene MP:0009084 blind uterus IEA N RGD:5509061 20210520 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20210128 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22415368 1321828 Stag1 STAG1 cohesin complex component gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321828 Stag1 STAG1 cohesin complex component gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321828 Stag1 STAG1 cohesin complex component gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22415365 1321832 Chchd4 coiled-coil-helix-coiled-coil-helix domain containing 4 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20190228 MGI PMID:26004228 1321832 Chchd4 coiled-coil-helix-coiled-coil-helix domain containing 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20190228 MGI PMID:26004228 1321832 Chchd4 coiled-coil-helix-coiled-coil-helix domain containing 4 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20190228 MGI PMID:26178476 1321832 Chchd4 coiled-coil-helix-coiled-coil-helix domain containing 4 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20190228 MGI PMID:26004228 1321832 Chchd4 coiled-coil-helix-coiled-coil-helix domain containing 4 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20190228 MGI PMID:26004228 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16554754 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12750314 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12750314 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:12750314 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:11439183 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12750314 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16554754 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:16554754 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12787506 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12787506 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16554754 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12750314 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12750314 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11439183 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12370307 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12787506 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:16554754 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20141003 MGI PMID:16554754 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11439183 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16554754 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12750314 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12750314 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:12750314 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:16554754 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16554754 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12750314 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:12370307 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:12750314 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12750314 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12370307 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12750314 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0006261 annular pancreas IAGP N RGD:5509061 20141003 MGI PMID:16554754 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16554754 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:12787506 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16554754 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:12750314 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12750314 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11439183 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11439183 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1321837 Nfatc4 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 4 gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:12750314 1321840 Agap3 ArfGAP with GTPase domain, ankyrin repeat and PH domain 3 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20210722 MGI PMID:33811862 1321840 Agap3 ArfGAP with GTPase domain, ankyrin repeat and PH domain 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210722 MGI PMID:33811862 1321840 Agap3 ArfGAP with GTPase domain, ankyrin repeat and PH domain 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210722 MGI PMID:33811862 1321840 Agap3 ArfGAP with GTPase domain, ankyrin repeat and PH domain 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20210722 MGI PMID:33811862 1321840 Agap3 ArfGAP with GTPase domain, ankyrin repeat and PH domain 3 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20210722 MGI PMID:33811862 1321840 Agap3 ArfGAP with GTPase domain, ankyrin repeat and PH domain 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210722 MGI PMID:33811862 1321840 Agap3 ArfGAP with GTPase domain, ankyrin repeat and PH domain 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:33811862 1321843 D430041D05Rik RIKEN cDNA D430041D05 gene gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20141003 MGI 1321843 D430041D05Rik RIKEN cDNA D430041D05 gene gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20141003 MGI 1321843 D430041D05Rik RIKEN cDNA D430041D05 gene gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1321845 Cxxc1 CXXC finger protein 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20230727 MGI PMID:35918532 1321845 Cxxc1 CXXC finger protein 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20230727 MGI PMID:35918532 1321845 Cxxc1 CXXC finger protein 1 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20160728 MGI PMID:11604496 1321845 Cxxc1 CXXC finger protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20230727 MGI PMID:35918532 1321845 Cxxc1 CXXC finger protein 1 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20230727 MGI PMID:35918532 1321845 Cxxc1 CXXC finger protein 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20230727 MGI PMID:35918532 1321845 Cxxc1 CXXC finger protein 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230727 MGI PMID:35918532 1321845 Cxxc1 CXXC finger protein 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20230727 MGI PMID:35918532 1321845 Cxxc1 CXXC finger protein 1 gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20160728 MGI PMID:11604496 1321845 Cxxc1 CXXC finger protein 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20230727 MGI PMID:35918532 1321845 Cxxc1 CXXC finger protein 1 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20230727 MGI PMID:35918532 1321845 Cxxc1 CXXC finger protein 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20230727 MGI PMID:35918532 1321845 Cxxc1 CXXC finger protein 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20230727 MGI PMID:35918532 1321845 Cxxc1 CXXC finger protein 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20230727 MGI PMID:35918532 1321845 Cxxc1 CXXC finger protein 1 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20141003 MGI PMID:11604496 1321845 Cxxc1 CXXC finger protein 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11604496 1321845 Cxxc1 CXXC finger protein 1 gene MP:0011184 absent embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:11604496 1321845 Cxxc1 CXXC finger protein 1 gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20230727 MGI PMID:35918532 1321845 Cxxc1 CXXC finger protein 1 gene MP:0013207 absent endoderm IAGP N RGD:5509061 20160728 MGI PMID:11604496 1321845 Cxxc1 CXXC finger protein 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20230727 MGI PMID:35918532 1321849 Ifi30 interferon gamma inducible protein 30 gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11701933 1321851 Asb1 ankyrin repeat and SOCS box-containing 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1321851 Asb1 ankyrin repeat and SOCS box-containing 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1321851 Asb1 ankyrin repeat and SOCS box-containing 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:11509662 1321851 Asb1 ankyrin repeat and SOCS box-containing 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11509662 1321851 Asb1 ankyrin repeat and SOCS box-containing 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:11509662 1321851 Asb1 ankyrin repeat and SOCS box-containing 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11509662 1321851 Asb1 ankyrin repeat and SOCS box-containing 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:11509662 1321851 Asb1 ankyrin repeat and SOCS box-containing 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 1321851 Asb1 ankyrin repeat and SOCS box-containing 1 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20220519 MGI 1321851 Asb1 ankyrin repeat and SOCS box-containing 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20220519 MGI 1321851 Asb1 ankyrin repeat and SOCS box-containing 1 gene MP:0013520 increased CD4-positive NK T cell number IEA N RGD:5509061 20240523 MGI 1321855 Nlk nemo like kinase gene MP:0000168 abnormal bone marrow development IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23719801 1321855 Nlk nemo like kinase gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1321855 Nlk nemo like kinase gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23719801 1321855 Nlk nemo like kinase gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1321855 Nlk nemo like kinase gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1321855 Nlk nemo like kinase gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1321855 Nlk nemo like kinase gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:23719801 1321855 Nlk nemo like kinase gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23719801 1321855 Nlk nemo like kinase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11745377 1321855 Nlk nemo like kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321857 Endog endonuclease G gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170105 MGI 1321857 Endog endonuclease G gene MP:0001147 small testis IEA N RGD:5509061 20170105 MGI 1321857 Endog endonuclease G gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20170105 MGI 1321857 Endog endonuclease G gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20230601 MGI 1321857 Endog endonuclease G gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15601850 1321857 Endog endonuclease G gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16239930 1321857 Endog endonuclease G gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14663139 1321857 Endog endonuclease G gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:14663139 1321857 Endog endonuclease G gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:14663139 1321857 Endog endonuclease G gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14663139 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0004892 increased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20160414 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:19156225 1321862 Itprid2 ITPR interacting domain containing 2 gene MP:0031414 decreased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:19156225 1321864 Dsc1 desmocollin 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0001247 dermal cyst IAGP N RGD:5509061 20160317 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14673151 1321864 Dsc1 desmocollin 1 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0004241 acantholysis IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0010700 hair follicle comedo IAGP N RGD:5509061 20160317 MGI PMID:11714727 1321864 Dsc1 desmocollin 1 gene MP:0030533 abnormal snout skin morphology IAGP N RGD:5509061 20180118 MGI PMID:11714727 1321874 Tmem9b TMEM9 domain family, member B gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1321874 Tmem9b TMEM9 domain family, member B gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1321874 Tmem9b TMEM9 domain family, member B gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1321874 Tmem9b TMEM9 domain family, member B gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20181227 MGI 1321874 Tmem9b TMEM9 domain family, member B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:16424905 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:17143286 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:17143286 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:17143286 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0003213 decreased susceptibility to age related obesity IAGP N RGD:5509061 20200310 MGI PMID:16424905 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:17143286 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20200310 MGI PMID:17143286 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20200310 MGI PMID:17143286 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:16424905 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17143286 1321875 Zfand5 zinc finger, AN1-type domain 5 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20200310 MGI PMID:17143286 1321876 Rftn1 raftlin lipid raft linker 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:19414744 1321876 Rftn1 raftlin lipid raft linker 1 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19414744 1321876 Rftn1 raftlin lipid raft linker 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:19414744 1321876 Rftn1 raftlin lipid raft linker 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19414744 1321876 Rftn1 raftlin lipid raft linker 1 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:19414744 1321876 Rftn1 raftlin lipid raft linker 1 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19414744 1321876 Rftn1 raftlin lipid raft linker 1 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:19414744 1321881 Hoxb3 homeobox B3 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:14960494 1321881 Hoxb3 homeobox B3 gene MP:0001051 abnormal somatic motor system morphology IAGP N RGD:5509061 20141003 MGI PMID:12954718 1321881 Hoxb3 homeobox B3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12748289 1321881 Hoxb3 homeobox B3 gene MP:0002256 abnormal laryngeal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7913519 1321881 Hoxb3 homeobox B3 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20141003 MGI PMID:9520319 1321881 Hoxb3 homeobox B3 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7913519 1321881 Hoxb3 homeobox B3 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0003955 abnormal ultimobranchial body morphology IAGP N RGD:5509061 20141003 MGI PMID:9520319 1321881 Hoxb3 homeobox B3 gene MP:0004445 small exoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0004568 fusion of glossopharyngeal and vagus nerve IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:7913519 1321881 Hoxb3 homeobox B3 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0004914 absent ultimobranchial body IAGP N RGD:5509061 20150122 MGI PMID:9520319 1321881 Hoxb3 homeobox B3 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0009899 hyoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7913519 1321881 Hoxb3 homeobox B3 gene MP:0009913 abnormal hyoid bone greater horn morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0010701 fusion of atlas and odontoid process IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0011576 absent cervical atlas IAGP N RGD:5509061 20141003 MGI PMID:7913519 1321881 Hoxb3 homeobox B3 gene MP:0013162 abnormal thyroid gland isthmus morphology IAGP N RGD:5509061 20141003 MGI PMID:9520319 1321881 Hoxb3 homeobox B3 gene MP:0013163 absent thyroid gland isthmus IAGP N RGD:5509061 20141003 MGI PMID:9520319 1321881 Hoxb3 homeobox B3 gene MP:0013290 persistent ultimobranchial bodies IAGP N RGD:5509061 20150122 MGI PMID:9520319 1321881 Hoxb3 homeobox B3 gene MP:0013574 ectopic parathyroid gland IAGP N RGD:5509061 20150305 MGI PMID:9520319 1321881 Hoxb3 homeobox B3 gene MP:0030869 thyroid cartilage hypoplasia IAGP N RGD:5509061 20181101 MGI PMID:9441667 1321881 Hoxb3 homeobox B3 gene MP:0030871 abnormal inferior horn of thyroid cartilage morphology IAGP N RGD:5509061 20181101 MGI PMID:7913519 1321881 Hoxb3 homeobox B3 gene MP:0030872 small cricoid cartilage IAGP N RGD:5509061 20181101 MGI PMID:9441667 1321892 Lao1 L-amino acid oxidase 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180607 MGI PMID:19276171 1321892 Lao1 L-amino acid oxidase 1 gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20180607 MGI PMID:19276171 1321892 Lao1 L-amino acid oxidase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180607 MGI PMID:19276171 1321892 Lao1 L-amino acid oxidase 1 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20180607 MGI PMID:19276171 1321892 Lao1 L-amino acid oxidase 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20180607 MGI PMID:19276171 1321892 Lao1 L-amino acid oxidase 1 gene MP:0013148 mastitis IAGP N RGD:5509061 20180607 MGI PMID:19276171 1321893 Hvcn1 hydrogen voltage-gated channel 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:19285483 1321893 Hvcn1 hydrogen voltage-gated channel 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:19285483 1321898 Six2 sine oculis-related homeobox 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221124 MGI PMID:31765609 1321898 Six2 sine oculis-related homeobox 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20221124 MGI PMID:31765609 1321898 Six2 sine oculis-related homeobox 2 gene MP:0000445 short snout IAGP N RGD:5509061 20221124 MGI PMID:31765609 1321898 Six2 sine oculis-related homeobox 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17036046 1321898 Six2 sine oculis-related homeobox 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0000524 decreased renal tubule number IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:17036046 1321898 Six2 sine oculis-related homeobox 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:18682239 1321898 Six2 sine oculis-related homeobox 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:20299358 1321898 Six2 sine oculis-related homeobox 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20200310 MGI PMID:30046000 1321898 Six2 sine oculis-related homeobox 2 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:18682239 1321898 Six2 sine oculis-related homeobox 2 gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0001426 polydipsia IAGP N RGD:5509061 20200310 MGI PMID:30046000 1321898 Six2 sine oculis-related homeobox 2 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20200310 MGI PMID:30046000 1321898 Six2 sine oculis-related homeobox 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20200310 MGI PMID:30046000 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23360989 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17036046 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:23360989 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:30046000 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18682239 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20053786 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:20299358 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:20299358 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20230323 MGI PMID:33514561 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20230323 MGI PMID:33514561 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20200310 MGI PMID:30046000 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:17036046 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:20299358 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:23360989 1321898 Six2 sine oculis-related homeobox 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20200310 MGI PMID:30046000 1321898 Six2 sine oculis-related homeobox 2 gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20200310 MGI PMID:30046000 1321898 Six2 sine oculis-related homeobox 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17036046 1321898 Six2 sine oculis-related homeobox 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0003624 anuria IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:17036046 1321898 Six2 sine oculis-related homeobox 2 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:23360989 1321898 Six2 sine oculis-related homeobox 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:23360989 1321898 Six2 sine oculis-related homeobox 2 gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0004755 abnormal loop of Henle morphology IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23360989 1321898 Six2 sine oculis-related homeobox 2 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:30046000 1321898 Six2 sine oculis-related homeobox 2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17036046 1321898 Six2 sine oculis-related homeobox 2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:20299358 1321898 Six2 sine oculis-related homeobox 2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20230323 MGI PMID:33514561 1321898 Six2 sine oculis-related homeobox 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20230323 MGI PMID:33514561 1321898 Six2 sine oculis-related homeobox 2 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20230323 MGI PMID:33514561 1321898 Six2 sine oculis-related homeobox 2 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:20299358 1321898 Six2 sine oculis-related homeobox 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221124 MGI PMID:31765609 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17036046 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18682239 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20299358 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20210603 MGI PMID:27542690 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221124 MGI PMID:31765609 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011289 abnormal nephron number IAGP N RGD:5509061 20141003 MGI PMID:17036046 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20299358 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20230323 MGI PMID:33514561 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20141003 MGI PMID:23360989 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011364 abnormal metanephros morphology IAGP N RGD:5509061 20141003 MGI PMID:23555292 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011371 decreased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23360989 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011387 absent metanephric mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:20299358 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011402 renal cast IAGP N RGD:5509061 20230323 MGI PMID:33514561 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20230323 MGI PMID:33514561 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011457 abnormal metanephric ureteric bud development IAGP N RGD:5509061 20141003 MGI PMID:20299358 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:20299358 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20230323 MGI PMID:33514561 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011856 abnormal glomerular filtration barrier function IAGP N RGD:5509061 20230323 MGI PMID:33514561 1321898 Six2 sine oculis-related homeobox 2 gene MP:0011869 detached podocyte IAGP N RGD:5509061 20230323 MGI PMID:33514561 1321898 Six2 sine oculis-related homeobox 2 gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20221124 MGI PMID:31765609 1321898 Six2 sine oculis-related homeobox 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:31765609 1321898 Six2 sine oculis-related homeobox 2 gene MP:0021217 abnormal palatal shelf bone ossification IAGP N RGD:5509061 20230302 MGI PMID:31765609 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20230119 MGI 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19561613 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230119 MGI 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20230119 MGI 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0001264 increased body size IEA N RGD:5509061 20141003 MGI 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0001326 retina degeneration IEA N RGD:5509061 20141003 MGI 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19561613 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20141003 MGI 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:19561613 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0003728 abnormal retina photoreceptor layer morphology IEA N RGD:5509061 20141003 MGI 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0003732 abnormal retina outer plexiform layer morphology IEA N RGD:5509061 20141003 MGI 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19561613 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19561613 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19561613 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19561613 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19561613 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19561613 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20230119 MGI 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19561613 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:19561613 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:19561613 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:19561613 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0008515 thin retina outer nuclear layer IEA N RGD:5509061 20141003 MGI 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:19561613 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20230119 MGI 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20141003 MGI 1321900 Rras2 related RAS viral (r-ras) oncogene 2 gene MP:0014348 decreased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:19561613 1321903 Kremen2 kringle containing transmembrane protein 2 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:18505822 1321903 Kremen2 kringle containing transmembrane protein 2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:18505822 1321903 Kremen2 kringle containing transmembrane protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18505822 1321903 Kremen2 kringle containing transmembrane protein 2 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:18505822 1321903 Kremen2 kringle containing transmembrane protein 2 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:18505822 1321903 Kremen2 kringle containing transmembrane protein 2 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:18505822 1321903 Kremen2 kringle containing transmembrane protein 2 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:18505822 1321903 Kremen2 kringle containing transmembrane protein 2 gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:18505822 1321908 Chst4 carbohydrate sulfotransferase 4 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:11520459 1321908 Chst4 carbohydrate sulfotransferase 4 gene MP:0002345 abnormal lymph node primary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11520459 1321908 Chst4 carbohydrate sulfotransferase 4 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:11520459 1321908 Chst4 carbohydrate sulfotransferase 4 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:14593101 1321908 Chst4 carbohydrate sulfotransferase 4 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:23254996 1321908 Chst4 carbohydrate sulfotransferase 4 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:11520459 1321908 Chst4 carbohydrate sulfotransferase 4 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:14593101 1321910 Fam53b family with sequence similarity 53, member B gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160421 MGI 1321910 Fam53b family with sequence similarity 53, member B gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20160421 MGI 1321910 Fam53b family with sequence similarity 53, member B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1321910 Fam53b family with sequence similarity 53, member B gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160421 MGI 1321910 Fam53b family with sequence similarity 53, member B gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1321910 Fam53b family with sequence similarity 53, member B gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1321910 Fam53b family with sequence similarity 53, member B gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20160421 MGI 1321910 Fam53b family with sequence similarity 53, member B gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20170105 MGI 1321910 Fam53b family with sequence similarity 53, member B gene MP:0011951 increased cardiac stroke volume IEA N RGD:5509061 20211021 MGI 1321912 Pcif1 phosphorylated CTD interacting factor 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20221215 MGI 1321912 Pcif1 phosphorylated CTD interacting factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200917 MGI PMID:32814042 1321912 Pcif1 phosphorylated CTD interacting factor 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1321912 Pcif1 phosphorylated CTD interacting factor 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 1321912 Pcif1 phosphorylated CTD interacting factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200917 MGI PMID:32814042 1321912 Pcif1 phosphorylated CTD interacting factor 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20221215 MGI 1321912 Pcif1 phosphorylated CTD interacting factor 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20221215 MGI 1321912 Pcif1 phosphorylated CTD interacting factor 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20221215 MGI 1321912 Pcif1 phosphorylated CTD interacting factor 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20240523 MGI 1321912 Pcif1 phosphorylated CTD interacting factor 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20231207 MGI 1321912 Pcif1 phosphorylated CTD interacting factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1321912 Pcif1 phosphorylated CTD interacting factor 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220811 MGI 1321916 Gabpa GA repeat binding protein, alpha gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1321916 Gabpa GA repeat binding protein, alpha gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20181227 MGI 1321916 Gabpa GA repeat binding protein, alpha gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1321916 Gabpa GA repeat binding protein, alpha gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1321916 Gabpa GA repeat binding protein, alpha gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:15361867 1321916 Gabpa GA repeat binding protein, alpha gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:15361867 1321916 Gabpa GA repeat binding protein, alpha gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:17325042 1321916 Gabpa GA repeat binding protein, alpha gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1321916 Gabpa GA repeat binding protein, alpha gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1321916 Gabpa GA repeat binding protein, alpha gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1321916 Gabpa GA repeat binding protein, alpha gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20181227 MGI 1321916 Gabpa GA repeat binding protein, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17485447 1321916 Gabpa GA repeat binding protein, alpha gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17325042 1321916 Gabpa GA repeat binding protein, alpha gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1321916 Gabpa GA repeat binding protein, alpha gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:17325042 1321916 Gabpa GA repeat binding protein, alpha gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20210520 MGI 1321916 Gabpa GA repeat binding protein, alpha gene MP:0003903 increased cell mass IAGP N RGD:5509061 20141003 MGI PMID:17277770 1321916 Gabpa GA repeat binding protein, alpha gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:17325042 1321916 Gabpa GA repeat binding protein, alpha gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:17277770 1321916 Gabpa GA repeat binding protein, alpha gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:15361867 1321916 Gabpa GA repeat binding protein, alpha gene MP:0004836 abnormal synaptic acetylcholine release IAGP N RGD:5509061 20141003 MGI PMID:17325042 1321916 Gabpa GA repeat binding protein, alpha gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1321916 Gabpa GA repeat binding protein, alpha gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15199140 1321916 Gabpa GA repeat binding protein, alpha gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17485447 1321916 Gabpa GA repeat binding protein, alpha gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15361867 1321916 Gabpa GA repeat binding protein, alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321916 Gabpa GA repeat binding protein, alpha gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:17277770 1321916 Gabpa GA repeat binding protein, alpha gene MP:0021086 decreased DNA replication IAGP N RGD:5509061 20220310 MGI PMID:17277770 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0000562 polydactyly IEA N RGD:5509061 20210520 MGI 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20170105 MGI 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0000914 exencephaly IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20170105 MGI 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0001265 decreased body size IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0001293 anophthalmia IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0001297 microphthalmia IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20170105 MGI 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20180118 MGI PMID:24889031 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20170105 MGI 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170105 MGI 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0002989 small kidney IEA N RGD:5509061 20170105 MGI 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20180118 MGI PMID:24889031 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0003717 pallor IEA N RGD:5509061 20181227 MGI 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20180118 MGI PMID:24889031 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20180118 MGI PMID:24889031 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0008797 facial cleft IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20180118 MGI PMID:24889031 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0012117 decreased trophectoderm cell proliferation IAGP N RGD:5509061 20180118 MGI PMID:24889031 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0012128 abnormal blastocyst formation IAGP N RGD:5509061 20180118 MGI PMID:24889031 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20180118 MGI PMID:24889031 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321921 Mmachc methylmalonic aciduria cblC type, with homocystinuria gene MP:0030630 increased circulating methylmalonic acid level IAGP N RGD:5509061 20210128 MGI PMID:32941884 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20160929 MGI PMID:27534441 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200109 MGI PMID:27162334 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0003381 vitreal fibroplasia IEA N RGD:5509061 20111116 MGI 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:12651948 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12651948 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19679561 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12651948 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19679561 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:12651948 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:19679561 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:19679561 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:19679561 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:19679561 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20171207 MGI PMID:28859131 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20171207 MGI PMID:28859131 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20171207 MGI PMID:28859131 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20171207 MGI PMID:28859131 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0012671 retina spots IEA N RGD:5509061 20141003 MGI 1321923 Rpgrip1 retinitis pigmentosa GTPase regulator interacting protein 1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:28859131 1321925 Hsf4 heat shock transcription factor 4 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15343150 1321925 Hsf4 heat shock transcription factor 4 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15593327 1321925 Hsf4 heat shock transcription factor 4 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:15483628 1321925 Hsf4 heat shock transcription factor 4 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:15593327 1321925 Hsf4 heat shock transcription factor 4 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:19224648 1321925 Hsf4 heat shock transcription factor 4 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:15343150 1321925 Hsf4 heat shock transcription factor 4 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:15483628 1321925 Hsf4 heat shock transcription factor 4 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:15593327 1321925 Hsf4 heat shock transcription factor 4 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:19224648 1321925 Hsf4 heat shock transcription factor 4 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:22162625 1321925 Hsf4 heat shock transcription factor 4 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:15343150 1321925 Hsf4 heat shock transcription factor 4 gene MP:0001309 hydropic eye lens fibers IAGP N RGD:5509061 20141003 MGI PMID:15483628 1321925 Hsf4 heat shock transcription factor 4 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20220519 MGI 1321925 Hsf4 heat shock transcription factor 4 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20220519 MGI 1321925 Hsf4 heat shock transcription factor 4 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15343150 1321925 Hsf4 heat shock transcription factor 4 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15593327 1321925 Hsf4 heat shock transcription factor 4 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19224648 1321925 Hsf4 heat shock transcription factor 4 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1321925 Hsf4 heat shock transcription factor 4 gene MP:0003236 abnormal lens capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:15483628 1321925 Hsf4 heat shock transcription factor 4 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15343150 1321925 Hsf4 heat shock transcription factor 4 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15483628 1321925 Hsf4 heat shock transcription factor 4 gene MP:0005102 abnormal iris pigmentation IEA N RGD:5509061 20220519 MGI 1321925 Hsf4 heat shock transcription factor 4 gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20141003 MGI PMID:15483628 1321925 Hsf4 heat shock transcription factor 4 gene MP:0031428 lens dislocation IAGP N RGD:5509061 20220714 MGI PMID:15343150 1321927 Lancl2 LanC (bacterial lantibiotic synthetase component C)-like 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1321927 Lancl2 LanC (bacterial lantibiotic synthetase component C)-like 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1321927 Lancl2 LanC (bacterial lantibiotic synthetase component C)-like 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20230601 MGI 1321927 Lancl2 LanC (bacterial lantibiotic synthetase component C)-like 2 gene MP:0002083 premature death IAGP N RGD:5509061 20240222 MGI PMID:33932340 1321927 Lancl2 LanC (bacterial lantibiotic synthetase component C)-like 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170105 MGI 1321927 Lancl2 LanC (bacterial lantibiotic synthetase component C)-like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180222 MGI PMID:28106097 1321927 Lancl2 LanC (bacterial lantibiotic synthetase component C)-like 2 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20240222 MGI PMID:27936058 1321927 Lancl2 LanC (bacterial lantibiotic synthetase component C)-like 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20170105 MGI 1321927 Lancl2 LanC (bacterial lantibiotic synthetase component C)-like 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20240222 MGI PMID:27936058 1321927 Lancl2 LanC (bacterial lantibiotic synthetase component C)-like 2 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20240222 MGI PMID:27936058 1321928 Pomk protein-O-mannose kinase gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20230601 MGI 1321928 Pomk protein-O-mannose kinase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1321928 Pomk protein-O-mannose kinase gene MP:0002635 reduced sensorimotor gating IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230601 MGI 1321928 Pomk protein-O-mannose kinase gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0010008 abnormal Purkinje cell migration IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321928 Pomk protein-O-mannose kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1321928 Pomk protein-O-mannose kinase gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20141003 MGI PMID:21746835 1321930 Aass aminoadipate-semialdehyde synthase gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210826 MGI 1321930 Aass aminoadipate-semialdehyde synthase gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1321930 Aass aminoadipate-semialdehyde synthase gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210826 MGI 1321932 Tchp trichoplein, keratin filament binding gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20201022 MGI 1321932 Tchp trichoplein, keratin filament binding gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160114 MGI 1321932 Tchp trichoplein, keratin filament binding gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20210527 MGI PMID:33691104 1321932 Tchp trichoplein, keratin filament binding gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20160114 MGI 1321932 Tchp trichoplein, keratin filament binding gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20210527 MGI PMID:33691104 1321932 Tchp trichoplein, keratin filament binding gene MP:0005358 abnormal incisor morphology IEA N RGD:5509061 20201022 MGI 1321932 Tchp trichoplein, keratin filament binding gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20210527 MGI PMID:33691104 1321932 Tchp trichoplein, keratin filament binding gene MP:0005533 increased body temperature IAGP N RGD:5509061 20210527 MGI PMID:33691104 1321932 Tchp trichoplein, keratin filament binding gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20210527 MGI PMID:33691104 1321932 Tchp trichoplein, keratin filament binding gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20210527 MGI PMID:33691104 1321932 Tchp trichoplein, keratin filament binding gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20210527 MGI PMID:33691104 1321932 Tchp trichoplein, keratin filament binding gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20210527 MGI PMID:33691104 1321932 Tchp trichoplein, keratin filament binding gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20210527 MGI PMID:33691104 1321932 Tchp trichoplein, keratin filament binding gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20210527 MGI PMID:33691104 1321932 Tchp trichoplein, keratin filament binding gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:33691104 1321934 Fanci Fanconi anemia, complementation group I gene MP:0000120 malocclusion IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0001116 small gonad IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0001117 absent gametes IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0001147 small testis IAGP N RGD:5509061 20211209 MGI PMID:34373449 1321934 Fanci Fanconi anemia, complementation group I gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20211209 MGI PMID:34373449 1321934 Fanci Fanconi anemia, complementation group I gene MP:0001262 decreased body weight IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0001265 decreased body size IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0001297 microphthalmia IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0001925 male infertility IAGP N RGD:5509061 20211209 MGI PMID:34373449 1321934 Fanci Fanconi anemia, complementation group I gene MP:0001925 male infertility IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0001926 female infertility IAGP N RGD:5509061 20211209 MGI PMID:34373449 1321934 Fanci Fanconi anemia, complementation group I gene MP:0001926 female infertility IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20211209 MGI PMID:34373449 1321934 Fanci Fanconi anemia, complementation group I gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20211209 MGI PMID:34373449 1321934 Fanci Fanconi anemia, complementation group I gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20211209 MGI PMID:34373449 1321934 Fanci Fanconi anemia, complementation group I gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20211209 MGI PMID:34373449 1321934 Fanci Fanconi anemia, complementation group I gene MP:0005159 azoospermia IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0008730 fused phalanges IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20211209 MGI PMID:34373449 1321934 Fanci Fanconi anemia, complementation group I gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0010772 abnormal pollex morphology IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1321934 Fanci Fanconi anemia, complementation group I gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0013707 abnormal hematopoietic precursor cell morphology IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0014040 increased cellular sensitivity to DNA damaging agents IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321934 Fanci Fanconi anemia, complementation group I gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20211209 MGI PMID:34373449 1321934 Fanci Fanconi anemia, complementation group I gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20211216 MGI PMID:31219578 1321935 Klhl25 kelch-like 25 gene MP:0013129 abnormal tooth color IEA N RGD:5509061 20181122 MGI 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15383458 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15834123 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0009623 enlarged inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11371358 1321938 Gpr132 G protein-coupled receptor 132 gene MP:0011081 decreased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15834123 1321939 Obox6 oocyte specific homeobox 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17676645 1321940 Cracdl capping protein inhibiting regulator of actin like gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1321940 Cracdl capping protein inhibiting regulator of actin like gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20201022 MGI 1321940 Cracdl capping protein inhibiting regulator of actin like gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1321940 Cracdl capping protein inhibiting regulator of actin like gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20201022 MGI 1321940 Cracdl capping protein inhibiting regulator of actin like gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20201022 MGI 1321942 Col15a1 collagen, type XV, alpha 1 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:11158616 1321942 Col15a1 collagen, type XV, alpha 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11158616 1321942 Col15a1 collagen, type XV, alpha 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:11158616 1321942 Col15a1 collagen, type XV, alpha 1 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:11158616 1321942 Col15a1 collagen, type XV, alpha 1 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11158616 1321942 Col15a1 collagen, type XV, alpha 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11158616 1321942 Col15a1 collagen, type XV, alpha 1 gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:11158616 1321944 Dolk dolichol kinase gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191205 MGI 1321944 Dolk dolichol kinase gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191205 MGI 1321944 Dolk dolichol kinase gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191205 MGI 1321944 Dolk dolichol kinase gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1321944 Dolk dolichol kinase gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191205 MGI 1321944 Dolk dolichol kinase gene MP:0003107 abnormal response to novelty IEA N RGD:5509061 20170413 MGI 1321944 Dolk dolichol kinase gene MP:0003360 abnormal depression-related behavior IEA N RGD:5509061 20170413 MGI 1321944 Dolk dolichol kinase gene MP:0005407 hyperalgesia IEA N RGD:5509061 20170413 MGI 1321944 Dolk dolichol kinase gene MP:0009331 absent primitive node IEA N RGD:5509061 20191205 MGI 1321944 Dolk dolichol kinase gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1321944 Dolk dolichol kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170413 MGI 1321944 Dolk dolichol kinase gene MP:0012724 absent head fold IEA N RGD:5509061 20191205 MGI 1321944 Dolk dolichol kinase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191205 MGI 1321945 Cttnbp2nl CTTNBP2 N-terminal like gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1321945 Cttnbp2nl CTTNBP2 N-terminal like gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 1321945 Cttnbp2nl CTTNBP2 N-terminal like gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20220811 MGI 1321945 Cttnbp2nl CTTNBP2 N-terminal like gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1321947 Recql5 RecQ protein-like 5 gene MP:0003701 elevated level of mitotic sister chromatid exchange IAGP N RGD:5509061 20141003 MGI PMID:15831450 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:23172145 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:23172145 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:23172145 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16237163 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:23172145 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:16237163 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:23172145 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16237163 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23172145 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23172145 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:23172145 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23172145 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:23172145 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0014373 increased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:23172145 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0014375 increased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:23172145 1321949 Eif4ebp2 eukaryotic translation initiation factor 4E binding protein 2 gene MP:0014384 increased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:23172145 1321951 Pgbd5 piggyBac transposable element derived 5 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20181227 MGI 1321951 Pgbd5 piggyBac transposable element derived 5 gene MP:0001293 anophthalmia IEA N RGD:5509061 20181227 MGI 1321951 Pgbd5 piggyBac transposable element derived 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1321951 Pgbd5 piggyBac transposable element derived 5 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1321951 Pgbd5 piggyBac transposable element derived 5 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20181227 MGI 1321951 Pgbd5 piggyBac transposable element derived 5 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20231207 MGI 1321951 Pgbd5 piggyBac transposable element derived 5 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20240404 MGI PMID:38517960 1321951 Pgbd5 piggyBac transposable element derived 5 gene MP:0009454 impaired contextual conditioning behavior IEA N RGD:5509061 20210128 MGI 1321951 Pgbd5 piggyBac transposable element derived 5 gene MP:0009516 enlarged salivary gland IEA N RGD:5509061 20181227 MGI 1321951 Pgbd5 piggyBac transposable element derived 5 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1321951 Pgbd5 piggyBac transposable element derived 5 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1321951 Pgbd5 piggyBac transposable element derived 5 gene MP:0010283 decreased classified tumor incidence IAGP N RGD:5509061 20240404 MGI PMID:38517960 1321951 Pgbd5 piggyBac transposable element derived 5 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20240404 MGI PMID:38517960 1321953 Actr2 actin related protein 2 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20180322 MGI PMID:28827327 1321954 Tril TLR4 interactor with leucine-rich repeats gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20210401 MGI PMID:25015823 1321954 Tril TLR4 interactor with leucine-rich repeats gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20210401 MGI PMID:25015823 1321954 Tril TLR4 interactor with leucine-rich repeats gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20210401 MGI PMID:25015823 1321954 Tril TLR4 interactor with leucine-rich repeats gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20210401 MGI PMID:25015823 1321954 Tril TLR4 interactor with leucine-rich repeats gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20210401 MGI PMID:25015823 1321955 Tmem129 transmembrane protein 129 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1321955 Tmem129 transmembrane protein 129 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1321955 Tmem129 transmembrane protein 129 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1321955 Tmem129 transmembrane protein 129 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220519 MGI 1321955 Tmem129 transmembrane protein 129 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1321955 Tmem129 transmembrane protein 129 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1321955 Tmem129 transmembrane protein 129 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220519 MGI 1321962 Riok3 RIO kinase 3 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1321962 Riok3 RIO kinase 3 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1321962 Riok3 RIO kinase 3 gene MP:0001925 male infertility IEA N RGD:5509061 20230601 MGI 1321962 Riok3 RIO kinase 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1321962 Riok3 RIO kinase 3 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20240523 MGI 1321967 Ptges2 prostaglandin E synthase 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23624557 1321967 Ptges2 prostaglandin E synthase 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1321967 Ptges2 prostaglandin E synthase 2 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23624557 1321968 Lpcat2b lysophosphatidylcholine acyltransferase 2B gene MP:0005544 cornea deposits IEA N RGD:5509061 20181227 MGI 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24141881 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:24141881 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160825 MGI PMID:14634087 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:24141881 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:24141881 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:24141881 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:24141881 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0004340 short scapula IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0008312 abnormal sympathetic postganglionic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0009891 abnormal palate bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0010405 ostium secundum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0010587 conotruncal ridge hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0010589 common truncal valve IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0010652 absent aorticopulmonary septum IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19412548 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24141881 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0030168 thin upper lip IAGP N RGD:5509061 20171005 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0030243 abnormal chin morphology IAGP N RGD:5509061 20171019 MGI PMID:17652350 1321970 Pds5b PDS5 cohesin associated factor B gene MP:0030244 short chin IAGP N RGD:5509061 20171019 MGI PMID:17652350 1321973 Tagln2 transgelin 2 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1321973 Tagln2 transgelin 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1321973 Tagln2 transgelin 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1321973 Tagln2 transgelin 2 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20180315 MGI PMID:25869671 1321973 Tagln2 transgelin 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1321973 Tagln2 transgelin 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20180315 MGI PMID:25869671 1321973 Tagln2 transgelin 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1321973 Tagln2 transgelin 2 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1321973 Tagln2 transgelin 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1321973 Tagln2 transgelin 2 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20180315 MGI PMID:25869671 1321973 Tagln2 transgelin 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 1321973 Tagln2 transgelin 2 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20211021 MGI 1321975 Zbtb21 zinc finger and BTB domain containing 21 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20240815 MGI PMID:38959316 1321980 Dusp10 dual specificity phosphatase 10 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:15306813 1321980 Dusp10 dual specificity phosphatase 10 gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:15306813 1321980 Dusp10 dual specificity phosphatase 10 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15306813 1321980 Dusp10 dual specificity phosphatase 10 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:15306813 1321980 Dusp10 dual specificity phosphatase 10 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15306813 1321980 Dusp10 dual specificity phosphatase 10 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:15306813 1321980 Dusp10 dual specificity phosphatase 10 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15306813 1321980 Dusp10 dual specificity phosphatase 10 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15306813 1321980 Dusp10 dual specificity phosphatase 10 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:15306813 1321984 Slc26a7 solute carrier family 26, member 7 gene MP:0000525 renal tubular acidosis IAGP N RGD:5509061 20141003 MGI PMID:19723628 1321984 Slc26a7 solute carrier family 26, member 7 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:19723628 1321984 Slc26a7 solute carrier family 26, member 7 gene MP:0002876 abnormal thyroid gland physiology IAGP N RGD:5509061 20220630 MGI PMID:30333321 1321984 Slc26a7 solute carrier family 26, member 7 gene MP:0003017 decreased circulating bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:19723628 1321984 Slc26a7 solute carrier family 26, member 7 gene MP:0003030 acidemia IAGP N RGD:5509061 20141003 MGI PMID:19723628 1321984 Slc26a7 solute carrier family 26, member 7 gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20220630 MGI PMID:30333321 1321984 Slc26a7 solute carrier family 26, member 7 gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:19723628 1321984 Slc26a7 solute carrier family 26, member 7 gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20220630 MGI PMID:30333321 1321984 Slc26a7 solute carrier family 26, member 7 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20220630 MGI PMID:30333321 1321984 Slc26a7 solute carrier family 26, member 7 gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20220630 MGI PMID:30333321 1321984 Slc26a7 solute carrier family 26, member 7 gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20220630 MGI PMID:30333321 1321984 Slc26a7 solute carrier family 26, member 7 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20220630 MGI PMID:30333321 1321984 Slc26a7 solute carrier family 26, member 7 gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20220630 MGI PMID:30333321 1321984 Slc26a7 solute carrier family 26, member 7 gene MP:0008055 increased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:19723628 1321984 Slc26a7 solute carrier family 26, member 7 gene MP:0009349 increased urine pH IAGP N RGD:5509061 20141003 MGI PMID:19723628 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20220825 MGI PMID:35044787 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230119 MGI 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0001925 male infertility IEA N RGD:5509061 20230119 MGI 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230119 MGI 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20220825 MGI PMID:35044787 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20220825 MGI PMID:35044787 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20220825 MGI PMID:35044787 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20220825 MGI PMID:35044787 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20220825 MGI PMID:35044787 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20220825 MGI PMID:35044787 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20220825 MGI PMID:35044787 1321986 Bag5 BCL2-associated athanogene 5 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:35044787 1321988 Gpr22 G protein-coupled receptor 22 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1321988 Gpr22 G protein-coupled receptor 22 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1321988 Gpr22 G protein-coupled receptor 22 gene MP:0001406 abnormal gait IEA N RGD:5509061 20170105 MGI 1321988 Gpr22 G protein-coupled receptor 22 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1321988 Gpr22 G protein-coupled receptor 22 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18539757 1321988 Gpr22 G protein-coupled receptor 22 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1321988 Gpr22 G protein-coupled receptor 22 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20240627 MGI 1321988 Gpr22 G protein-coupled receptor 22 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1321988 Gpr22 G protein-coupled receptor 22 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160421 MGI 1321988 Gpr22 G protein-coupled receptor 22 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:18539757 1321988 Gpr22 G protein-coupled receptor 22 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1321988 Gpr22 G protein-coupled receptor 22 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1321988 Gpr22 G protein-coupled receptor 22 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1321988 Gpr22 G protein-coupled receptor 22 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20211021 MGI 1321988 Gpr22 G protein-coupled receptor 22 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 1321990 Ipo7 importin 7 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210520 MGI 1321990 Ipo7 importin 7 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1321990 Ipo7 importin 7 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1321990 Ipo7 importin 7 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1321990 Ipo7 importin 7 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1321990 Ipo7 importin 7 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1321990 Ipo7 importin 7 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220519 MGI 1321990 Ipo7 importin 7 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1321990 Ipo7 importin 7 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20221215 MGI 1321990 Ipo7 importin 7 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1321990 Ipo7 importin 7 gene MP:0002282 abnormal trachea morphology IEA N RGD:5509061 20210520 MGI 1321990 Ipo7 importin 7 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1321990 Ipo7 importin 7 gene MP:0004957 abnormal blastocyst morphology IEA N RGD:5509061 20240919 MGI 1321990 Ipo7 importin 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1321990 Ipo7 importin 7 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1321990 Ipo7 importin 7 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240919 MGI 1321991 Asb18 ankyrin repeat and SOCS box-containing 18 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1321993 Camsap1 calmodulin regulated spectrin-associated protein 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20201105 MGI PMID:32839317 1321993 Camsap1 calmodulin regulated spectrin-associated protein 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20201105 MGI PMID:32839317 1321993 Camsap1 calmodulin regulated spectrin-associated protein 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20221215 MGI 1321993 Camsap1 calmodulin regulated spectrin-associated protein 1 gene MP:0002064 seizures IAGP N RGD:5509061 20201105 MGI PMID:32839317 1321993 Camsap1 calmodulin regulated spectrin-associated protein 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20201105 MGI PMID:32839317 1321993 Camsap1 calmodulin regulated spectrin-associated protein 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20221215 MGI 1321993 Camsap1 calmodulin regulated spectrin-associated protein 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20201105 MGI PMID:32839317 1321993 Camsap1 calmodulin regulated spectrin-associated protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1321993 Camsap1 calmodulin regulated spectrin-associated protein 1 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20201105 MGI PMID:32839317 1321993 Camsap1 calmodulin regulated spectrin-associated protein 1 gene MP:0020581 abnormal neuron polarity IAGP N RGD:5509061 20201105 MGI PMID:32839317 1321993 Camsap1 calmodulin regulated spectrin-associated protein 1 gene MP:0020850 abnormal microtubule cytoskeleton morphology IAGP N RGD:5509061 20201105 MGI PMID:32839317 1321996 Phf11d PHD finger protein 11D gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20151022 MGI PMID:25091723 1322001 Coq5 coenzyme Q5 methyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1322003 Grsf1 G-rich RNA sequence binding factor 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1322005 Ushbp1 USH1 protein network component harmonin binding protein 1 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20160114 MGI 1322011 Slc39a3 solute carrier family 39 (zinc transporter), member 3 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:16652366 1322011 Slc39a3 solute carrier family 39 (zinc transporter), member 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:16652366 1322011 Slc39a3 solute carrier family 39 (zinc transporter), member 3 gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15964816 1322011 Slc39a3 solute carrier family 39 (zinc transporter), member 3 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:15964816 1322011 Slc39a3 solute carrier family 39 (zinc transporter), member 3 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:16652366 1322011 Slc39a3 solute carrier family 39 (zinc transporter), member 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16652366 1322011 Slc39a3 solute carrier family 39 (zinc transporter), member 3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:15964816 1322011 Slc39a3 solute carrier family 39 (zinc transporter), member 3 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:16652366 1322011 Slc39a3 solute carrier family 39 (zinc transporter), member 3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15964816 1322013 Lyve1 lymphatic vessel endothelial hyaluronan receptor 1 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20026661 1322013 Lyve1 lymphatic vessel endothelial hyaluronan receptor 1 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20026661 1322013 Lyve1 lymphatic vessel endothelial hyaluronan receptor 1 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:20026661 1322013 Lyve1 lymphatic vessel endothelial hyaluronan receptor 1 gene MP:0002392 abnormal Peyer's patch T cell area morphology IAGP N RGD:5509061 20141003 MGI PMID:20026661 1322013 Lyve1 lymphatic vessel endothelial hyaluronan receptor 1 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:20026661 1322013 Lyve1 lymphatic vessel endothelial hyaluronan receptor 1 gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20141003 MGI PMID:17070806 1322013 Lyve1 lymphatic vessel endothelial hyaluronan receptor 1 gene MP:0004038 lymphangiectasis IAGP N RGD:5509061 20141003 MGI PMID:17070806 1322013 Lyve1 lymphatic vessel endothelial hyaluronan receptor 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20026661 1322013 Lyve1 lymphatic vessel endothelial hyaluronan receptor 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20026661 1322013 Lyve1 lymphatic vessel endothelial hyaluronan receptor 1 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:20026661 1322015 Krt7 keratin 7 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1322015 Krt7 keratin 7 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210128 MGI 1322015 Krt7 keratin 7 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23741325 1322015 Krt7 keratin 7 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20210128 MGI 1322015 Krt7 keratin 7 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:23741325 1322018 Pitpnm2 phosphatidylinositol transfer protein, membrane-associated 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11744244 1322019 Engase endo-beta-N-acetylglucosaminidase gene MP:0001513 limb grasping IAGP N RGD:5509061 20210923 MGI PMID:34215698 1322027 Trabd TraB domain containing gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210520 MGI 1322029 Il22ra2 interleukin 22 receptor, alpha 2 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23075849 1322029 Il22ra2 interleukin 22 receptor, alpha 2 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:23075849 1322029 Il22ra2 interleukin 22 receptor, alpha 2 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23075849 1322029 Il22ra2 interleukin 22 receptor, alpha 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23075849 1322029 Il22ra2 interleukin 22 receptor, alpha 2 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:23075849 1322031 Yeats2 YEATS domain containing 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1322031 Yeats2 YEATS domain containing 2 gene MP:0001513 limb grasping IEA N RGD:5509061 20210128 MGI 1322031 Yeats2 YEATS domain containing 2 gene MP:0001523 impaired righting response IEA N RGD:5509061 20210128 MGI 1322031 Yeats2 YEATS domain containing 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 1322031 Yeats2 YEATS domain containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322031 Yeats2 YEATS domain containing 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1322032 Mthfd2l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2-like gene MP:0000274 enlarged heart IEA N RGD:5509061 20160811 MGI 1322032 Mthfd2l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2-like gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20160811 MGI 1322032 Mthfd2l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2-like gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 1322036 Terf2 telomeric repeat binding factor 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17015429 1322036 Terf2 telomeric repeat binding factor 2 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17015429 1322036 Terf2 telomeric repeat binding factor 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15968270 1322038 Parvg parvin, gamma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16479001 1322040 Fpr1 formyl peptide receptor 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9989980 1322040 Fpr1 formyl peptide receptor 1 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:9989980 1322040 Fpr1 formyl peptide receptor 1 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:9989980 1322040 Fpr1 formyl peptide receptor 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9989980 1322042 Barx1 BarH-like homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22084104 1322042 Barx1 BarH-like homeobox 1 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:22084104 1322042 Barx1 BarH-like homeobox 1 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:22084104 1322042 Barx1 BarH-like homeobox 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22084104 1322042 Barx1 BarH-like homeobox 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22084104 1322042 Barx1 BarH-like homeobox 1 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:15809042 1322042 Barx1 BarH-like homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22084104 1322042 Barx1 BarH-like homeobox 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15809042 1322044 Diablo diablo, IAP-binding mitochondrial protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15509788 1322044 Diablo diablo, IAP-binding mitochondrial protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15509788 1322044 Diablo diablo, IAP-binding mitochondrial protein gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:15509788 1322044 Diablo diablo, IAP-binding mitochondrial protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11971981 1322044 Diablo diablo, IAP-binding mitochondrial protein gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15509788 1322046 Zfat zinc finger and AT hook domain containing gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1322046 Zfat zinc finger and AT hook domain containing gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1322046 Zfat zinc finger and AT hook domain containing gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1322046 Zfat zinc finger and AT hook domain containing gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1322046 Zfat zinc finger and AT hook domain containing gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1322046 Zfat zinc finger and AT hook domain containing gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1322046 Zfat zinc finger and AT hook domain containing gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:20660741 1322046 Zfat zinc finger and AT hook domain containing gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230119 MGI 1322046 Zfat zinc finger and AT hook domain containing gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20660741 1322046 Zfat zinc finger and AT hook domain containing gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:20660741 1322046 Zfat zinc finger and AT hook domain containing gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20660741 1322046 Zfat zinc finger and AT hook domain containing gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22828507 1322046 Zfat zinc finger and AT hook domain containing gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22828507 1322046 Zfat zinc finger and AT hook domain containing gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22828507 1322046 Zfat zinc finger and AT hook domain containing gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22828507 1322046 Zfat zinc finger and AT hook domain containing gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22828507 1322046 Zfat zinc finger and AT hook domain containing gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22828507 1322046 Zfat zinc finger and AT hook domain containing gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:22828507 1322046 Zfat zinc finger and AT hook domain containing gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20190307 MGI PMID:30106088 1322046 Zfat zinc finger and AT hook domain containing gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20660741 1322046 Zfat zinc finger and AT hook domain containing gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1322046 Zfat zinc finger and AT hook domain containing gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20141003 MGI PMID:20660741 1322046 Zfat zinc finger and AT hook domain containing gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20240523 MGI 1322048 Miga2 mitoguardin 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20141003 MGI 1322048 Miga2 mitoguardin 2 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 1322048 Miga2 mitoguardin 2 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1322048 Miga2 mitoguardin 2 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20160804 MGI 1322048 Miga2 mitoguardin 2 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20160804 MGI 1322048 Miga2 mitoguardin 2 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20160804 MGI 1322048 Miga2 mitoguardin 2 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20160804 MGI 1322048 Miga2 mitoguardin 2 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20240926 MGI PMID:31675497 1322048 Miga2 mitoguardin 2 gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20240926 MGI PMID:31675497 1322048 Miga2 mitoguardin 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20141003 MGI 1322048 Miga2 mitoguardin 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1322048 Miga2 mitoguardin 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20240926 MGI PMID:31675497 1322048 Miga2 mitoguardin 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160804 MGI 1322048 Miga2 mitoguardin 2 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20141003 MGI 1322048 Miga2 mitoguardin 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20240926 MGI PMID:31675497 1322048 Miga2 mitoguardin 2 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20240926 MGI PMID:31675497 1322048 Miga2 mitoguardin 2 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20240926 MGI PMID:31675497 1322048 Miga2 mitoguardin 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20160804 MGI 1322048 Miga2 mitoguardin 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20141003 MGI 1322048 Miga2 mitoguardin 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1322048 Miga2 mitoguardin 2 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1322048 Miga2 mitoguardin 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20141003 MGI 1322048 Miga2 mitoguardin 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20240926 MGI PMID:31675497 1322048 Miga2 mitoguardin 2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20141003 MGI 1322048 Miga2 mitoguardin 2 gene MP:0005571 decreased lactate dehydrogenase level IEA N RGD:5509061 20160804 MGI 1322048 Miga2 mitoguardin 2 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 1322048 Miga2 mitoguardin 2 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20240926 MGI PMID:31675497 1322048 Miga2 mitoguardin 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1322048 Miga2 mitoguardin 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20141003 MGI 1322048 Miga2 mitoguardin 2 gene MP:0012479 increased amygdala size IAGP N RGD:5509061 20240926 MGI PMID:31675497 1322048 Miga2 mitoguardin 2 gene MP:0014414 increased depression-related behavior IAGP N RGD:5509061 20240926 MGI PMID:31675497 1322048 Miga2 mitoguardin 2 gene MP:0014416 decreased social novelty preference IAGP N RGD:5509061 20240926 MGI PMID:31675497 1322048 Miga2 mitoguardin 2 gene MP:0014527 increased amino acid level IAGP N RGD:5509061 20240926 MGI PMID:31675497 1322048 Miga2 mitoguardin 2 gene MP:0031487 increased circulating hypoxanthine level IAGP N RGD:5509061 20240926 MGI PMID:31675497 1322048 Miga2 mitoguardin 2 gene MP:0031490 increased circulating xanthine level IAGP N RGD:5509061 20240926 MGI PMID:31675497 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:23382243 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23382243 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:23382243 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10892650 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17210695 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:17210695 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11201745 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10892650 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:23382243 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20141003 MGI PMID:17210695 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:16476774 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:17210695 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:23382243 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:11201745 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:10892650 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:10892650 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:23382243 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17210695 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:10892650 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:23187126 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0009759 abnormal hair follicle bulge morphology IAGP N RGD:5509061 20181220 MGI PMID:23382243 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20141003 MGI PMID:10892650 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20141003 MGI PMID:17210695 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10892650 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23382243 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10892650 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0011194 abnormal hair follicle physiology IAGP N RGD:5509061 20141003 MGI PMID:23382243 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:10892650 1322051 Mad2l1 MAD2 mitotic arrest deficient-like 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:10892650 1322053 Ptgir prostaglandin I receptor (IP) gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:11964481 1322053 Ptgir prostaglandin I receptor (IP) gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11964481 1322053 Ptgir prostaglandin I receptor (IP) gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:9262402 1322053 Ptgir prostaglandin I receptor (IP) gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:9262402 1322053 Ptgir prostaglandin I receptor (IP) gene MP:0005413 vascular restenosis IAGP N RGD:5509061 20141003 MGI PMID:11964481 1322053 Ptgir prostaglandin I receptor (IP) gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20200917 MGI PMID:11964481 1322053 Ptgir prostaglandin I receptor (IP) gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:9262402 1322053 Ptgir prostaglandin I receptor (IP) gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:9262402 1322053 Ptgir prostaglandin I receptor (IP) gene MP:0009818 abnormal thromboxane level IAGP N RGD:5509061 20141003 MGI PMID:11964481 1322053 Ptgir prostaglandin I receptor (IP) gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9262402 1322053 Ptgir prostaglandin I receptor (IP) gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:16614756 1322053 Ptgir prostaglandin I receptor (IP) gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:9262402 1322061 Kbtbd3 kelch repeat and BTB (POZ) domain containing 3 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230601 MGI 1322061 Kbtbd3 kelch repeat and BTB (POZ) domain containing 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1322061 Kbtbd3 kelch repeat and BTB (POZ) domain containing 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1322065 Pmm1 phosphomannomutase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16847318 1322067 Scml4 Scm polycomb group protein like 4 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1322067 Scml4 Scm polycomb group protein like 4 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20190502 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0000274 enlarged heart IEA N RGD:5509061 20190502 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20190502 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201231 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20241010 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0001698 decreased embryo size IEA N RGD:5509061 20241010 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20241010 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20231207 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0009331 absent primitive node IEA N RGD:5509061 20241010 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0009709 hydrometra IEA N RGD:5509061 20190502 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0012724 absent head fold IEA N RGD:5509061 20241010 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1322071 Mtpap mitochondrial poly(A) polymerase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1322073 Dpp8 dipeptidylpeptidase 8 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210826 MGI 1322073 Dpp8 dipeptidylpeptidase 8 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1322073 Dpp8 dipeptidylpeptidase 8 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1322073 Dpp8 dipeptidylpeptidase 8 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20210826 MGI 1322073 Dpp8 dipeptidylpeptidase 8 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20240523 MGI 1322073 Dpp8 dipeptidylpeptidase 8 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20210826 MGI 1322073 Dpp8 dipeptidylpeptidase 8 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210826 MGI 1322073 Dpp8 dipeptidylpeptidase 8 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210826 MGI 1322073 Dpp8 dipeptidylpeptidase 8 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1322073 Dpp8 dipeptidylpeptidase 8 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210826 MGI 1322073 Dpp8 dipeptidylpeptidase 8 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220519 MGI 1322073 Dpp8 dipeptidylpeptidase 8 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 1322073 Dpp8 dipeptidylpeptidase 8 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210826 MGI 1322073 Dpp8 dipeptidylpeptidase 8 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210826 MGI 1322073 Dpp8 dipeptidylpeptidase 8 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220519 MGI 1322075 Nudt12 nudix hydrolase 12 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20200109 MGI PMID:31875550 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0000745 tremors IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0001265 decreased body size IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0001577 anemia IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20230601 MGI 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0002083 premature death IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0004259 small placenta IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0004266 pale placenta IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0011527 disorganized placental labyrinth IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0011531 abnormal syncytiotrophoblast morphology IAGP N RGD:5509061 20190207 MGI PMID:28708136 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20230601 MGI 1322083 Tlk2 tousled-like kinase 2 (Arabidopsis) gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20191219 MGI PMID:28708136 1322087 Sema6d sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20190912 MGI PMID:28172500 1322087 Sema6d sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20190912 MGI PMID:28172500 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0001263 weight loss IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0001406 abnormal gait IEA N RGD:5509061 20210520 MGI 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0002083 premature death IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0002704 tubular nephritis IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0003670 dilated renal glomerular capsule IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0005556 abnormal renal filtration rate IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0011483 renal glomerular synechia IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0011509 dilated glomerular capillary IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322089 Cmas cytidine monophospho-N-acetylneuraminic acid synthetase gene MP:0011868 podocyte microvillus transformation IAGP N RGD:5509061 20200416 MGI PMID:31040189 1322091 Eps8l2 EPS8-like 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210128 MGI 1322091 Eps8l2 EPS8-like 2 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20181227 MGI 1322091 Eps8l2 EPS8-like 2 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1322091 Eps8l2 EPS8-like 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20181227 MGI 1322091 Eps8l2 EPS8-like 2 gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20181227 MGI 1322091 Eps8l2 EPS8-like 2 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23918390 1322091 Eps8l2 EPS8-like 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200402 MGI 1322091 Eps8l2 EPS8-like 2 gene MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:23918390 1322091 Eps8l2 EPS8-like 2 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:23918390 1322091 Eps8l2 EPS8-like 2 gene MP:0004524 short cochlear hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:23918390 1322091 Eps8l2 EPS8-like 2 gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:23918390 1322091 Eps8l2 EPS8-like 2 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:23918390 1322091 Eps8l2 EPS8-like 2 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23918390 1322091 Eps8l2 EPS8-like 2 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:23918390 1322091 Eps8l2 EPS8-like 2 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1322091 Eps8l2 EPS8-like 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1322091 Eps8l2 EPS8-like 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1322091 Eps8l2 EPS8-like 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1322091 Eps8l2 EPS8-like 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:23918390 1322091 Eps8l2 EPS8-like 2 gene MP:0006335 abnormal hearing electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23918390 1322091 Eps8l2 EPS8-like 2 gene MP:0006388 abnormal auditory summating potential IAGP N RGD:5509061 20141003 MGI PMID:23918390 1322091 Eps8l2 EPS8-like 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1322091 Eps8l2 EPS8-like 2 gene MP:0009456 impaired cued conditioning behavior IEA N RGD:5509061 20230601 MGI 1322091 Eps8l2 EPS8-like 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20181227 MGI 1322091 Eps8l2 EPS8-like 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23918390 1322094 Pip5k1b phosphatidylinositol-4-phosphate 5-kinase, type 1 beta gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:22321832 1322094 Pip5k1b phosphatidylinositol-4-phosphate 5-kinase, type 1 beta gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:22321832 1322094 Pip5k1b phosphatidylinositol-4-phosphate 5-kinase, type 1 beta gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:22321832 1322094 Pip5k1b phosphatidylinositol-4-phosphate 5-kinase, type 1 beta gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22321832 1322094 Pip5k1b phosphatidylinositol-4-phosphate 5-kinase, type 1 beta gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:22321832 1322094 Pip5k1b phosphatidylinositol-4-phosphate 5-kinase, type 1 beta gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15767368 1322094 Pip5k1b phosphatidylinositol-4-phosphate 5-kinase, type 1 beta gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22321832 1322094 Pip5k1b phosphatidylinositol-4-phosphate 5-kinase, type 1 beta gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22321832 1322094 Pip5k1b phosphatidylinositol-4-phosphate 5-kinase, type 1 beta gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20141003 MGI PMID:22321832 1322094 Pip5k1b phosphatidylinositol-4-phosphate 5-kinase, type 1 beta gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22321832 1322094 Pip5k1b phosphatidylinositol-4-phosphate 5-kinase, type 1 beta gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:15767368 1322094 Pip5k1b phosphatidylinositol-4-phosphate 5-kinase, type 1 beta gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:22321832 1322094 Pip5k1b phosphatidylinositol-4-phosphate 5-kinase, type 1 beta gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:22321832 1322094 Pip5k1b phosphatidylinositol-4-phosphate 5-kinase, type 1 beta gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:22321832 1322094 Pip5k1b phosphatidylinositol-4-phosphate 5-kinase, type 1 beta gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:22321832 1322099 Igdcc4 immunoglobulin superfamily, DCC subclass, member 4 gene MP:0020947 decreased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20220224 MGI PMID:34871331 1322099 Igdcc4 immunoglobulin superfamily, DCC subclass, member 4 gene MP:0031045 decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20220224 MGI PMID:34871331 1322102 Snx14 sorting nexin 14 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1322102 Snx14 sorting nexin 14 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20201022 MGI 1322102 Snx14 sorting nexin 14 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1322102 Snx14 sorting nexin 14 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1322102 Snx14 sorting nexin 14 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322107 Dyrk3 dual-specificity tyrosine phosphorylation regulated kinase 3 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18854306 1322107 Dyrk3 dual-specificity tyrosine phosphorylation regulated kinase 3 gene MP:0031276 abnormal stress erythropoiesis IAGP N RGD:5509061 20210805 MGI PMID:18854306 1322108 Snrnp27 small nuclear ribonucleoprotein 27 (U4/U6.U5) gene MP:0000467 abnormal esophagus morphology IEA N RGD:5509061 20160811 MGI 1322108 Snrnp27 small nuclear ribonucleoprotein 27 (U4/U6.U5) gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1322108 Snrnp27 small nuclear ribonucleoprotein 27 (U4/U6.U5) gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1322108 Snrnp27 small nuclear ribonucleoprotein 27 (U4/U6.U5) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322108 Snrnp27 small nuclear ribonucleoprotein 27 (U4/U6.U5) gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20231207 MGI 1322108 Snrnp27 small nuclear ribonucleoprotein 27 (U4/U6.U5) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1322108 Snrnp27 small nuclear ribonucleoprotein 27 (U4/U6.U5) gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20170629 MGI PMID:27229122 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20170629 MGI PMID:27229122 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0002580 duodenal lesions IAGP N RGD:5509061 20170629 MGI PMID:27229122 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20170629 MGI PMID:27229122 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20170629 MGI PMID:27229122 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20170629 MGI PMID:27229122 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20170629 MGI PMID:27229122 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0009311 increased duodenum adenocarcinoma incidence IAGP N RGD:5509061 20170629 MGI PMID:27229122 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17517967 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0012408 increased duodenum glandular epithelium tumor incidence IAGP N RGD:5509061 20170629 MGI PMID:27229122 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0013482 abnormal duodenum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20170629 MGI PMID:27229122 1322109 B3gnt6 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:17517967 1322112 Xpo7 exportin 7 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20221215 MGI PMID:35973480 1322112 Xpo7 exportin 7 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20221215 MGI PMID:35973480 1322112 Xpo7 exportin 7 gene MP:0001577 anemia IAGP N RGD:5509061 20221215 MGI PMID:35973480 1322112 Xpo7 exportin 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20221215 MGI PMID:35973480 1322112 Xpo7 exportin 7 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20221215 MGI PMID:35973480 1322112 Xpo7 exportin 7 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20221215 MGI PMID:35973480 1322112 Xpo7 exportin 7 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20221215 MGI PMID:35973480 1322112 Xpo7 exportin 7 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20221215 MGI PMID:35973480 1322112 Xpo7 exportin 7 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20221215 MGI PMID:35973480 1322112 Xpo7 exportin 7 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20221215 MGI PMID:35973480 1322112 Xpo7 exportin 7 gene MP:0013659 abnormal erythroid lineage cell morphology IAGP N RGD:5509061 20221215 MGI PMID:35973480 1322112 Xpo7 exportin 7 gene MP:0031276 abnormal stress erythropoiesis IAGP N RGD:5509061 20221215 MGI PMID:35973480 1322116 Dppa3 developmental pluripotency-associated 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20211104 MGI PMID:26692333 1322116 Dppa3 developmental pluripotency-associated 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15018652 1322116 Dppa3 developmental pluripotency-associated 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14654002 1322116 Dppa3 developmental pluripotency-associated 3 gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:17143267 1322116 Dppa3 developmental pluripotency-associated 3 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:14654002 1322116 Dppa3 developmental pluripotency-associated 3 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20211104 MGI PMID:26692333 1322116 Dppa3 developmental pluripotency-associated 3 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20211104 MGI PMID:26692333 1322116 Dppa3 developmental pluripotency-associated 3 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20211104 MGI PMID:26692333 1322116 Dppa3 developmental pluripotency-associated 3 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20211104 MGI PMID:26692333 1322116 Dppa3 developmental pluripotency-associated 3 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20211104 MGI PMID:26692333 1322116 Dppa3 developmental pluripotency-associated 3 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:17143267 1322116 Dppa3 developmental pluripotency-associated 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21441929 1322125 Slc49a4 solute carrier family 49 member 4 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210520 MGI 1322125 Slc49a4 solute carrier family 49 member 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1322125 Slc49a4 solute carrier family 49 member 4 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20210520 MGI 1322127 Miga1 mitoguardin 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1322127 Miga1 mitoguardin 1 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1322127 Miga1 mitoguardin 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 1322127 Miga1 mitoguardin 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1322127 Miga1 mitoguardin 1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20160811 MGI 1322127 Miga1 mitoguardin 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1322130 Idua iduronidase, alpha-L gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:17101178 1322130 Idua iduronidase, alpha-L gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:17101178 1322130 Idua iduronidase, alpha-L gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20210930 MGI PMID:33905568 1322130 Idua iduronidase, alpha-L gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12576554 1322130 Idua iduronidase, alpha-L gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9097952 1322130 Idua iduronidase, alpha-L gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9097952 1322130 Idua iduronidase, alpha-L gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0000346 broad head IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:15111796 1322130 Idua iduronidase, alpha-L gene MP:0000441 increased cranium width IAGP N RGD:5509061 20170907 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0000445 short snout IAGP N RGD:5509061 20170907 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:9097952 1322130 Idua iduronidase, alpha-L gene MP:0000731 increased collagen deposition in the muscles IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9097952 1322130 Idua iduronidase, alpha-L gene MP:0001200 thick skin IEA N RGD:5509061 20240523 MGI 1322130 Idua iduronidase, alpha-L gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18022143 1322130 Idua iduronidase, alpha-L gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20170907 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1322130 Idua iduronidase, alpha-L gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20240523 MGI 1322130 Idua iduronidase, alpha-L gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1322130 Idua iduronidase, alpha-L gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18022143 1322130 Idua iduronidase, alpha-L gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18022143 1322130 Idua iduronidase, alpha-L gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0001462 abnormal avoidance learning behavior IAGP N RGD:5509061 20141003 MGI PMID:16473336 1322130 Idua iduronidase, alpha-L gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:18022143 1322130 Idua iduronidase, alpha-L gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18022143 1322130 Idua iduronidase, alpha-L gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:18511319 1322130 Idua iduronidase, alpha-L gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:17101178 1322130 Idua iduronidase, alpha-L gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:17101178 1322130 Idua iduronidase, alpha-L gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:18022143 1322130 Idua iduronidase, alpha-L gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19751987 1322130 Idua iduronidase, alpha-L gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9097952 1322130 Idua iduronidase, alpha-L gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:16473336 1322130 Idua iduronidase, alpha-L gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1322130 Idua iduronidase, alpha-L gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0002833 increased heart weight IAGP N RGD:5509061 20231109 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:17101178 1322130 Idua iduronidase, alpha-L gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9097952 1322130 Idua iduronidase, alpha-L gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15111796 1322130 Idua iduronidase, alpha-L gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:19751987 1322130 Idua iduronidase, alpha-L gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:18022143 1322130 Idua iduronidase, alpha-L gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12576554 1322130 Idua iduronidase, alpha-L gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0003898 abnormal QRS complex IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0003929 decreased heart rate variability IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12576554 1322130 Idua iduronidase, alpha-L gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17101178 1322130 Idua iduronidase, alpha-L gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15111796 1322130 Idua iduronidase, alpha-L gene MP:0004595 abnormal mandibular condyloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:15111796 1322130 Idua iduronidase, alpha-L gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240523 MGI 1322130 Idua iduronidase, alpha-L gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:17101178 1322130 Idua iduronidase, alpha-L gene MP:0004864 spiral ligament degeneration IAGP N RGD:5509061 20141003 MGI PMID:17101178 1322130 Idua iduronidase, alpha-L gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17101178 1322130 Idua iduronidase, alpha-L gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:19751987 1322130 Idua iduronidase, alpha-L gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20141003 MGI PMID:9097952 1322130 Idua iduronidase, alpha-L gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19751987 1322130 Idua iduronidase, alpha-L gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0005287 narrow eye opening IEA N RGD:5509061 20240523 MGI 1322130 Idua iduronidase, alpha-L gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:15111796 1322130 Idua iduronidase, alpha-L gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:19751987 1322130 Idua iduronidase, alpha-L gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0006033 abnormal external auditory canal morphology IAGP N RGD:5509061 20141003 MGI PMID:15111796 1322130 Idua iduronidase, alpha-L gene MP:0006045 mitral valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0006198 enophthalmos IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:19751987 1322130 Idua iduronidase, alpha-L gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:18022143 1322130 Idua iduronidase, alpha-L gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18022143 1322130 Idua iduronidase, alpha-L gene MP:0009840 abnormal foam cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19751987 1322130 Idua iduronidase, alpha-L gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20240523 MGI 1322130 Idua iduronidase, alpha-L gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15111796 1322130 Idua iduronidase, alpha-L gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1322130 Idua iduronidase, alpha-L gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0010429 abnormal heart left ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0010591 enlarged aortic valve IAGP N RGD:5509061 20231109 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20231109 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0010618 enlarged mitral valve IAGP N RGD:5509061 20231109 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0010627 enlarged tricuspid valve IAGP N RGD:5509061 20231109 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20210930 MGI PMID:33905568 1322130 Idua iduronidase, alpha-L gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20210930 MGI PMID:33905568 1322130 Idua iduronidase, alpha-L gene MP:0010941 abnormal foramen magnum morphology IAGP N RGD:5509061 20141003 MGI PMID:15111796 1322130 Idua iduronidase, alpha-L gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20171012 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0011021 abnormal circadian regulation of heart rate IAGP N RGD:5509061 20171012 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0011473 increased urine glycosaminoglycan level IAGP N RGD:5509061 20141003 MGI PMID:17920451 1322130 Idua iduronidase, alpha-L gene MP:0011473 increased urine glycosaminoglycan level IAGP N RGD:5509061 20141003 MGI PMID:18022143 1322130 Idua iduronidase, alpha-L gene MP:0011473 increased urine glycosaminoglycan level IAGP N RGD:5509061 20141003 MGI PMID:19751987 1322130 Idua iduronidase, alpha-L gene MP:0011473 increased urine glycosaminoglycan level IAGP N RGD:5509061 20141003 MGI PMID:9097952 1322130 Idua iduronidase, alpha-L gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20240523 MGI 1322130 Idua iduronidase, alpha-L gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17101178 1322130 Idua iduronidase, alpha-L gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20210930 MGI PMID:33905568 1322130 Idua iduronidase, alpha-L gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:19751987 1322130 Idua iduronidase, alpha-L gene MP:0020242 increased autopod size IAGP N RGD:5509061 20230824 MGI PMID:9097952 1322130 Idua iduronidase, alpha-L gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0021161 increased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0021163 increased heart left ventricle septal wall thickness IAGP N RGD:5509061 20231109 MGI PMID:15979918 1322130 Idua iduronidase, alpha-L gene MP:0030037 prominent nasal bridge IAGP N RGD:5509061 20170914 MGI PMID:9660052 1322130 Idua iduronidase, alpha-L gene MP:0030069 broad face IAGP N RGD:5509061 20170921 MGI PMID:9097952 1322130 Idua iduronidase, alpha-L gene MP:0030189 broad snout IAGP N RGD:5509061 20171019 MGI PMID:19751987 1322130 Idua iduronidase, alpha-L gene MP:0030796 hip dislocation IAGP N RGD:5509061 20181025 MGI PMID:9660052 1322132 Naa50 N(alpha)-acetyltransferase 50, NatE catalytic subunit gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1322132 Naa50 N(alpha)-acetyltransferase 50, NatE catalytic subunit gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1322132 Naa50 N(alpha)-acetyltransferase 50, NatE catalytic subunit gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1322132 Naa50 N(alpha)-acetyltransferase 50, NatE catalytic subunit gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1322132 Naa50 N(alpha)-acetyltransferase 50, NatE catalytic subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322132 Naa50 N(alpha)-acetyltransferase 50, NatE catalytic subunit gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1322132 Naa50 N(alpha)-acetyltransferase 50, NatE catalytic subunit gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1322135 Papolb poly (A) polymerase beta (testis specific) gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20201022 MGI 1322135 Papolb poly (A) polymerase beta (testis specific) gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1322135 Papolb poly (A) polymerase beta (testis specific) gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:12471261 1322135 Papolb poly (A) polymerase beta (testis specific) gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12471261 1322135 Papolb poly (A) polymerase beta (testis specific) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12471261 1322135 Papolb poly (A) polymerase beta (testis specific) gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12471261 1322135 Papolb poly (A) polymerase beta (testis specific) gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210520 MGI 1322135 Papolb poly (A) polymerase beta (testis specific) gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:12471261 1322137 Dynlt2a1 dynein light chain Tctex-type 2A1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19778998 1322137 Dynlt2a1 dynein light chain Tctex-type 2A1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19778998 1322137 Dynlt2a1 dynein light chain Tctex-type 2A1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19778998 1322137 Dynlt2a1 dynein light chain Tctex-type 2A1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19778998 1322137 Dynlt2a1 dynein light chain Tctex-type 2A1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19778998 1322137 Dynlt2a1 dynein light chain Tctex-type 2A1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19778998 1322137 Dynlt2a1 dynein light chain Tctex-type 2A1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:19778998 1322137 Dynlt2a1 dynein light chain Tctex-type 2A1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:19778998 1322137 Dynlt2a1 dynein light chain Tctex-type 2A1 gene MP:0009839 multiflagellated sperm IAGP N RGD:5509061 20141003 MGI PMID:19778998 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21746917 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001306 small lens IAGP N RGD:5509061 20160310 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10675333 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21746917 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:21746917 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:21746917 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21746917 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20160310 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21746917 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21746917 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21746917 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21746917 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0010405 ostium secundum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10675333 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21041952 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:9030684 1322141 Sos1 SOS Ras/Rac guanine nucleotide exchange factor 1 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20160310 MGI PMID:9030684 1322144 E130308A19Rik RIKEN cDNA E130308A19 gene gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1322144 E130308A19Rik RIKEN cDNA E130308A19 gene gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1322152 Slitrk5 SLIT and NTRK-like family, member 5 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:20418887 1322152 Slitrk5 SLIT and NTRK-like family, member 5 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20201022 MGI 1322152 Slitrk5 SLIT and NTRK-like family, member 5 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1322152 Slitrk5 SLIT and NTRK-like family, member 5 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:20418887 1322152 Slitrk5 SLIT and NTRK-like family, member 5 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20418887 1322152 Slitrk5 SLIT and NTRK-like family, member 5 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:20418887 1322152 Slitrk5 SLIT and NTRK-like family, member 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20418887 1322152 Slitrk5 SLIT and NTRK-like family, member 5 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1322152 Slitrk5 SLIT and NTRK-like family, member 5 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:20418887 1322152 Slitrk5 SLIT and NTRK-like family, member 5 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:20418887 1322152 Slitrk5 SLIT and NTRK-like family, member 5 gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20418887 1322152 Slitrk5 SLIT and NTRK-like family, member 5 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20418887 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230119 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20230119 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20240523 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230119 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230119 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20241010 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241010 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241010 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20241010 MGI 1322155 Clptm1 cleft lip and palate associated transmembrane protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230119 MGI 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0009898 maxillary shelf hypoplasia IAGP N RGD:5509061 20171109 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0030250 frontonasal prominence hypoplasia IAGP N RGD:5509061 20171019 MGI PMID:18385133 1322157 Ndst3 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20171109 MGI PMID:18385133 1322159 Ssr1 signal sequence receptor, alpha gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0000601 small liver IEA N RGD:5509061 20210826 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220519 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0001148 enlarged testis IEA N RGD:5509061 20220519 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220519 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0001304 cataract IEA N RGD:5509061 20220519 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20210520 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210520 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210520 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20210520 MGI 1322159 Ssr1 signal sequence receptor, alpha gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0010645 failure of conotruncal ridge closure IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0010651 aorticopulmonary septal defect IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17015483 1322159 Ssr1 signal sequence receptor, alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1322161 Btbd1 BTB domain containing 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1322161 Btbd1 BTB domain containing 1 gene MP:0003604 single kidney IEA N RGD:5509061 20200514 MGI 1322161 Btbd1 BTB domain containing 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20221215 MGI 1322161 Btbd1 BTB domain containing 1 gene MP:0013436 increased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20240523 MGI 1322161 Btbd1 BTB domain containing 1 gene MP:0013520 increased CD4-positive NK T cell number IEA N RGD:5509061 20240523 MGI 1322165 Ikzf5 IKAROS family zinc finger 5 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1322165 Ikzf5 IKAROS family zinc finger 5 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1322165 Ikzf5 IKAROS family zinc finger 5 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240627 MGI 1322165 Ikzf5 IKAROS family zinc finger 5 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1322165 Ikzf5 IKAROS family zinc finger 5 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 1322167 Dok2 docking protein 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15611294 1322167 Dok2 docking protein 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15611295 1322167 Dok2 docking protein 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20139980 1322167 Dok2 docking protein 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15611294 1322167 Dok2 docking protein 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15611295 1322167 Dok2 docking protein 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15611294 1322167 Dok2 docking protein 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15611295 1322167 Dok2 docking protein 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15611294 1322167 Dok2 docking protein 2 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:15611295 1322167 Dok2 docking protein 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15611294 1322167 Dok2 docking protein 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15611295 1322167 Dok2 docking protein 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15611294 1322167 Dok2 docking protein 2 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:15611294 1322167 Dok2 docking protein 2 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15611294 1322167 Dok2 docking protein 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20548287 1322167 Dok2 docking protein 2 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:15611294 1322167 Dok2 docking protein 2 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:15611295 1322167 Dok2 docking protein 2 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20139980 1322167 Dok2 docking protein 2 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15611294 1322167 Dok2 docking protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15611294 1322167 Dok2 docking protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15611295 1322167 Dok2 docking protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20139980 1322167 Dok2 docking protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20548287 1322167 Dok2 docking protein 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:20139980 1322167 Dok2 docking protein 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15611294 1322167 Dok2 docking protein 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15611295 1322167 Dok2 docking protein 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20548287 1322167 Dok2 docking protein 2 gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15611295 1322167 Dok2 docking protein 2 gene MP:0004202 pulmonary hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20139980 1322167 Dok2 docking protein 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:20548287 1322167 Dok2 docking protein 2 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:20139980 1322167 Dok2 docking protein 2 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20139980 1322167 Dok2 docking protein 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15611294 1322167 Dok2 docking protein 2 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20548287 1322167 Dok2 docking protein 2 gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:20139980 1322167 Dok2 docking protein 2 gene MP:0010829 increased bronchioalveolar stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20139980 1322167 Dok2 docking protein 2 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:15611294 1322169 Car13 carbonic anhydrase 13 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220811 MGI 1322172 Ino80 INO80 complex subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1322172 Ino80 INO80 complex subunit gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1322172 Ino80 INO80 complex subunit gene MP:0001513 limb grasping IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20210826 MGI 1322172 Ino80 INO80 complex subunit gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20160811 MGI 1322172 Ino80 INO80 complex subunit gene MP:0002083 premature death IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20151224 MGI 1322172 Ino80 INO80 complex subunit gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0005655 increased aggression IEA N RGD:5509061 20201231 MGI 1322172 Ino80 INO80 complex subunit gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0008402 increased cellular sensitivity to alkylating agents IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0008409 increased cellular sensitivity to hydroxyurea IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20210826 MGI 1322172 Ino80 INO80 complex subunit gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20160414 MGI PMID:26975355 1322172 Ino80 INO80 complex subunit gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1322172 Ino80 INO80 complex subunit gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322172 Ino80 INO80 complex subunit gene MP:0012159 absent anterior visceral endoderm IAGP N RGD:5509061 20160414 MGI PMID:26975355 1322172 Ino80 INO80 complex subunit gene MP:0012161 absent distal visceral endoderm IAGP N RGD:5509061 20160414 MGI PMID:26975355 1322172 Ino80 INO80 complex subunit gene MP:0012734 abnormal response to radiation IAGP N RGD:5509061 20170608 MGI PMID:23979016 1322174 Clasp1 CLIP associating protein 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1322174 Clasp1 CLIP associating protein 1 gene MP:0000599 enlarged liver IEA N RGD:5509061 20210128 MGI 1322174 Clasp1 CLIP associating protein 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1322174 Clasp1 CLIP associating protein 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1322174 Clasp1 CLIP associating protein 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1322174 Clasp1 CLIP associating protein 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1322174 Clasp1 CLIP associating protein 1 gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1322174 Clasp1 CLIP associating protein 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1322174 Clasp1 CLIP associating protein 1 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1322174 Clasp1 CLIP associating protein 1 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 1322174 Clasp1 CLIP associating protein 1 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 1322174 Clasp1 CLIP associating protein 1 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20221215 MGI 1322174 Clasp1 CLIP associating protein 1 gene MP:0009084 blind uterus IEA N RGD:5509061 20210826 MGI 1322174 Clasp1 CLIP associating protein 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20210826 MGI 1322174 Clasp1 CLIP associating protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1322174 Clasp1 CLIP associating protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1322176 Mtmr3 myotubularin related protein 3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230601 MGI 1322176 Mtmr3 myotubularin related protein 3 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1322176 Mtmr3 myotubularin related protein 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20111116 MGI 1322176 Mtmr3 myotubularin related protein 3 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20111116 MGI 1322176 Mtmr3 myotubularin related protein 3 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1322176 Mtmr3 myotubularin related protein 3 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20231207 MGI 1322176 Mtmr3 myotubularin related protein 3 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20220811 MGI 1322176 Mtmr3 myotubularin related protein 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1322179 Sorcs3 sortilin-related VPS10 domain containing receptor 3 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:24069373 1322179 Sorcs3 sortilin-related VPS10 domain containing receptor 3 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:24069373 1322179 Sorcs3 sortilin-related VPS10 domain containing receptor 3 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20141003 MGI PMID:24069373 1322179 Sorcs3 sortilin-related VPS10 domain containing receptor 3 gene MP:0012312 impaired avoidance learning behavior IAGP N RGD:5509061 20141003 MGI PMID:24069373 1322180 Pde12 phosphodiesterase 12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322180 Pde12 phosphodiesterase 12 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1322183 Epm2aip1 EPM2A interacting protein 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:24142699 1322183 Epm2aip1 EPM2A interacting protein 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24142699 1322183 Epm2aip1 EPM2A interacting protein 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:24142699 1322183 Epm2aip1 EPM2A interacting protein 1 gene MP:0003213 decreased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:24142699 1322183 Epm2aip1 EPM2A interacting protein 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:24142699 1322183 Epm2aip1 EPM2A interacting protein 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:24142699 1322183 Epm2aip1 EPM2A interacting protein 1 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24142699 1322183 Epm2aip1 EPM2A interacting protein 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:24142699 1322183 Epm2aip1 EPM2A interacting protein 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:24142699 1322185 Cst5 cystatin D gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:16680148 1322185 Cst5 cystatin D gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:16680148 1322185 Cst5 cystatin D gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:16680148 1322185 Cst5 cystatin D gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:16680148 1322185 Cst5 cystatin D gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16680148 1322185 Cst5 cystatin D gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:16680148 1322187 Thbs2 thrombospondin 2 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:9442117 1322187 Thbs2 thrombospondin 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:9442117 1322187 Thbs2 thrombospondin 2 gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:12213711 1322187 Thbs2 thrombospondin 2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11387198 1322187 Thbs2 thrombospondin 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1322187 Thbs2 thrombospondin 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1322187 Thbs2 thrombospondin 2 gene MP:0001158 abnormal prostate gland morphology IEA N RGD:5509061 20230119 MGI 1322187 Thbs2 thrombospondin 2 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:12213711 1322187 Thbs2 thrombospondin 2 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1322187 Thbs2 thrombospondin 2 gene MP:0001391 abnormal tail movements IAGP N RGD:5509061 20141003 MGI PMID:9442117 1322187 Thbs2 thrombospondin 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:9442117 1322187 Thbs2 thrombospondin 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12213711 1322187 Thbs2 thrombospondin 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9442117 1322187 Thbs2 thrombospondin 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1322187 Thbs2 thrombospondin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9442117 1322187 Thbs2 thrombospondin 2 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:12213711 1322187 Thbs2 thrombospondin 2 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:9442117 1322187 Thbs2 thrombospondin 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1322187 Thbs2 thrombospondin 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1322187 Thbs2 thrombospondin 2 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:10571734 1322187 Thbs2 thrombospondin 2 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:12213711 1322187 Thbs2 thrombospondin 2 gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 1322187 Thbs2 thrombospondin 2 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:9442117 1322187 Thbs2 thrombospondin 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12213711 1322187 Thbs2 thrombospondin 2 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:9442117 1322187 Thbs2 thrombospondin 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11387198 1322187 Thbs2 thrombospondin 2 gene MP:0004958 enlarged prostate gland IEA N RGD:5509061 20230119 MGI 1322187 Thbs2 thrombospondin 2 gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:9442117 1322187 Thbs2 thrombospondin 2 gene MP:0005504 abnormal ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:9442117 1322187 Thbs2 thrombospondin 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:9442117 1322187 Thbs2 thrombospondin 2 gene MP:0005507 tail dragging IAGP N RGD:5509061 20141003 MGI PMID:9442117 1322187 Thbs2 thrombospondin 2 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:9442117 1322187 Thbs2 thrombospondin 2 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20201002 MGI PMID:12213711 1322187 Thbs2 thrombospondin 2 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11387198 1322187 Thbs2 thrombospondin 2 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:9442117 1322187 Thbs2 thrombospondin 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12213711 1322187 Thbs2 thrombospondin 2 gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20181004 MGI PMID:9442117 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20170928 MGI 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:12514744 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12514744 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000414 alopecia IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000414 alopecia IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20170928 MGI PMID:11381623 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20170928 MGI PMID:11381623 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20160728 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001240 abnormal epidermis stratum corneum morphology IEA N RGD:5509061 20170928 MGI 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001280 loss of vibrissae IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001433 polyphagia IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:12514744 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:12514744 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0001874 acanthosis IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0002074 abnormal hair texture IEA N RGD:5509061 20170928 MGI 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0002991 abnormal sebaceous gland physiology IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0002991 abnormal sebaceous gland physiology IAGP N RGD:5509061 20170928 MGI PMID:11381623 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0002992 abnormal sebaceous lipid secretion IAGP N RGD:5509061 20170928 MGI PMID:11381623 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0003848 brittle hair IAGP N RGD:5509061 20141003 MGI PMID:12514744 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0003848 brittle hair IAGP N RGD:5509061 20170928 MGI PMID:11381623 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0003849 greasy coat IAGP N RGD:5509061 20141003 MGI PMID:12514744 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0003849 greasy coat IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0003875 abnormal hair follicle regression IAGP N RGD:5509061 20141003 MGI PMID:12514744 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0003981 decreased circulating phospholipid level IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0005081 abnormal dermis reticular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0009545 abnormal dermis papillary layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0009600 hypergranulosis IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0009792 seborrheic dermatitis IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0009793 sebaceous gland hypertrophy IAGP N RGD:5509061 20160728 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0009793 sebaceous gland hypertrophy IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20181129 MGI PMID:12514744 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:12514744 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0010206 pigment incontinence IAGP N RGD:5509061 20181129 MGI PMID:12514744 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0010699 dilated hair follicle IAGP N RGD:5509061 20160317 MGI PMID:15482472 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0013373 increased sebum secretion IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20170608 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20170615 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0030571 dilated piliary canal IAGP N RGD:5509061 20180524 MGI PMID:24531688 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:23715724 1322188 Mpzl3 myelin protein zero-like 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:23715724 1322190 Trim2 tripartite motif-containing 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:18687884 1322190 Trim2 tripartite motif-containing 2 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:18687884 1322190 Trim2 tripartite motif-containing 2 gene MP:0001314 cornea opacity IEA N RGD:5509061 20220811 MGI 1322190 Trim2 tripartite motif-containing 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18687884 1322190 Trim2 tripartite motif-containing 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:18687884 1322190 Trim2 tripartite motif-containing 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:18687884 1322190 Trim2 tripartite motif-containing 2 gene MP:0003043 hypoalgesia IEA N RGD:5509061 20220519 MGI 1322190 Trim2 tripartite motif-containing 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:18687884 1322190 Trim2 tripartite motif-containing 2 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:18687884 1322190 Trim2 tripartite motif-containing 2 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18687884 1322190 Trim2 tripartite motif-containing 2 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:18687884 1322190 Trim2 tripartite motif-containing 2 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:18687884 1322190 Trim2 tripartite motif-containing 2 gene MP:0009979 abnormal cerebellum deep nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18687884 1322192 Col16a1 collagen, type XVI, alpha 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1322192 Col16a1 collagen, type XVI, alpha 1 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1322192 Col16a1 collagen, type XVI, alpha 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1322192 Col16a1 collagen, type XVI, alpha 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 1322193 Tti1 TELO2 interacting protein 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1322193 Tti1 TELO2 interacting protein 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20240523 MGI 1322193 Tti1 TELO2 interacting protein 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1322193 Tti1 TELO2 interacting protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20141003 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20160421 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20160421 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20201231 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0000745 tremors IEA N RGD:5509061 20160421 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20160421 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0001413 abnormal response to new environment IEA N RGD:5509061 20141003 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210128 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160804 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20160804 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20160804 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20141003 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0004129 abnormal respiratory quotient IEA N RGD:5509061 20160804 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0005287 narrow eye opening IEA N RGD:5509061 20160421 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20141003 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160804 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20141003 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0006241 abnormal placement of pupils IEA N RGD:5509061 20141003 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20160804 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20160804 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20160804 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20160804 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20160421 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160421 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0011496 abnormal head size IEA N RGD:5509061 20201022 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0011999 abnormal tail length IEA N RGD:5509061 20201231 MGI 1322200 Cyb561 cytochrome b-561 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20111116 MGI 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12130661 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12130661 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20141003 MGI PMID:12130661 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:12130661 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:12446777 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12130661 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17723215 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:16304053 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0001606 impaired hematopoiesis IEA N RGD:5509061 20161201 MGI 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:12235209 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:12446777 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:20826752 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0001805 decreased IgG level IEA N RGD:5509061 20161201 MGI 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12130661 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12235209 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12130661 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16304053 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:12130661 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18412166 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12130661 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16304053 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12446777 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0002367 abnormal thymus lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:16304053 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:12130661 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:20826752 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16304053 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16114097 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12130661 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12446777 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:20826752 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:18412166 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:18178811 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12130661 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235209 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20111116 MGI 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16304053 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235209 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12446777 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16304053 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17723215 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20826752 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:17723215 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16304053 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12235209 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12446777 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16114097 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:17723215 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17723215 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16304053 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20826752 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16304053 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20826752 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008168 decreased B-1a cell number IEA N RGD:5509061 20161201 MGI 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18178811 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:20826752 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18178811 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235209 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008202 absent B-1 B cells IAGP N RGD:5509061 20141003 MGI PMID:12446777 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235209 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12446777 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:12130661 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:12446777 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:20826752 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:20826752 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12235209 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20826752 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12235209 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:12235209 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:12235209 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17723215 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008573 increased circulating interferon-alpha level IEA N RGD:5509061 20161201 MGI 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18412166 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:18412166 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0009548 abnormal platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:16011964 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0010187 decreased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:20826752 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:12446777 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20161201 MGI 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0020002 increased response to antigen IEA N RGD:5509061 20161201 MGI 1322206 Pik3cd phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta gene MP:0020916 increased susceptibility to Herpesvirales infection IEA N RGD:5509061 20200430 MGI 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20170831 MGI PMID:22246904 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20170831 MGI PMID:26989192 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21816367 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20170831 MGI PMID:22246904 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20230316 MGI PMID:35304452 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20230316 MGI PMID:35304452 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20170831 MGI PMID:22246904 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20171221 MGI PMID:28504700 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:23151479 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20170831 MGI PMID:26989192 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170831 MGI PMID:26989192 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21816367 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20170831 MGI PMID:22246904 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20170831 MGI PMID:26989192 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0001468 abnormal temporal memory IAGP N RGD:5509061 20141003 MGI PMID:23770080 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20171221 MGI PMID:28504700 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20240718 MGI PMID:33895792 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0001890 anencephaly IAGP N RGD:5509061 20170831 MGI PMID:26989192 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21816367 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23151479 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20171221 MGI PMID:28504700 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0003578 absent ovary IAGP N RGD:5509061 20141003 MGI PMID:23151479 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20170831 MGI PMID:26989192 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21816367 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:23151479 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:23770080 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:23151479 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20230316 MGI PMID:35304452 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:23151479 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20240718 MGI PMID:33895792 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20240718 MGI PMID:33895792 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20240718 MGI PMID:33895792 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20240718 MGI PMID:33895792 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0008818 abnormal interfrontal bone morphology IAGP N RGD:5509061 20170831 MGI PMID:22246904 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0008845 abnormal paraventricular hypothalamic nucleus morphology IAGP N RGD:5509061 20170831 MGI PMID:22246904 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0008846 abnormal supraoptic nucleus morphology IAGP N RGD:5509061 20170831 MGI PMID:22246904 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:23770080 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:23151479 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:21816367 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20171221 MGI PMID:28504700 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:23770080 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0010343 increased lipoma incidence IAGP N RGD:5509061 20170831 MGI PMID:22246904 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:23151479 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23151479 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20171221 MGI PMID:28504700 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20171221 MGI PMID:28504700 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23151479 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20171221 MGI PMID:28504700 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20171221 MGI PMID:28504700 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0011257 abnormal head fold morphology IAGP N RGD:5509061 20171221 MGI PMID:28504700 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0012260 encephalomeningocele IAGP N RGD:5509061 20170831 MGI PMID:26989192 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20141003 MGI PMID:23770080 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0012540 abnormal lamina terminalis morphology IAGP N RGD:5509061 20170831 MGI PMID:22246904 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0013302 increased pancreas iron level IAGP N RGD:5509061 20240718 MGI PMID:33895792 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0013507 increased ovary apoptosis IAGP N RGD:5509061 20220505 MGI PMID:23151479 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0013771 decreased effector memory T-helper cell number IAGP N RGD:5509061 20230316 MGI PMID:35304452 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0020385 decreased intestinal iron level IAGP N RGD:5509061 20240718 MGI PMID:33895792 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0030117 bifid nose IAGP N RGD:5509061 20171005 MGI PMID:26989192 1322210 Tet1 tet methylcytosine dioxygenase 1 gene MP:0031474 increased female germ cell apoptosis IAGP N RGD:5509061 20230615 MGI PMID:23151479 1322212 Irf2bpl interferon regulatory factor 2 binding protein-like gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1322212 Irf2bpl interferon regulatory factor 2 binding protein-like gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 1322212 Irf2bpl interferon regulatory factor 2 binding protein-like gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220519 MGI 1322214 Klk15 kallikrein related-peptidase 15 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20221215 MGI 1322214 Klk15 kallikrein related-peptidase 15 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20210128 MGI 1322214 Klk15 kallikrein related-peptidase 15 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210520 MGI 1322214 Klk15 kallikrein related-peptidase 15 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1322214 Klk15 kallikrein related-peptidase 15 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20210128 MGI 1322214 Klk15 kallikrein related-peptidase 15 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220519 MGI 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:21666053 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:21666053 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000162 lordosis IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21666053 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:17029558 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20141003 MGI 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:17029558 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000746 weakness IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:17029558 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001097 abnormal superior glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001101 abnormal superior vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001263 weight loss IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21666053 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001265 decreased body size IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20171228 MGI PMID:20057387 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:18682242 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21666053 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001785 edema IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:18682242 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:17029558 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20171228 MGI PMID:20057387 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18682242 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001914 hemorrhage IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001921 reduced fertility IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:17029558 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22084405 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21666053 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:17029558 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0002415 abnormal neutrophil differentiation IAGP N RGD:5509061 20141003 MGI PMID:17029558 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:17029558 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18682242 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21666053 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18682242 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004266 pale placenta IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004600 abnormal vertebral transverse process morphology IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004602 abnormal vertebral articular process morphology IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004622 sacral vertebral fusion IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004684 intervertebral disk degeneration IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:18682242 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18682242 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18682242 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21666053 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22084405 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0005504 abnormal ligament morphology IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0006018 abnormal tympanic membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17029558 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:17029558 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0006295 absent sclerotome IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0006320 abnormal interscapular fat pad morphology IAGP N RGD:5509061 20180111 MGI PMID:24703692 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0006325 impaired hearing IAGP N RGD:5509061 20171228 MGI PMID:20057387 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0006393 absent nucleus pulposus IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21666053 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21666053 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20180111 MGI PMID:24703692 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21666053 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0009877 exostosis IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0010113 abnormal sacrum morphology IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21666053 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22084405 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20150528 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17029558 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17029558 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18682242 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17029558 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18682242 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0011246 abnormal fetal liver hematopoietic progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18682242 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21666053 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0011642 abnormal bone collagen fibril morphology IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0012184 absent paraxial mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0012235 abnormal liver bud morphology IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0012249 absent myotome IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0013166 small forelimb buds IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0013168 absent hindlimb buds IAGP N RGD:5509061 20141003 MGI PMID:9256345 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0013176 abnormal tail position or orientation IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0014399 decreased hematopoietic precursor cell number IAGP N RGD:5509061 20240321 MGI PMID:24586749 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0030226 middle ear polyps IAGP N RGD:5509061 20171228 MGI PMID:20057387 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0030410 middle ear effusion IAGP N RGD:5509061 20171228 MGI PMID:20057387 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0030414 tympanic membrane perforation IAGP N RGD:5509061 20171207 MGI PMID:17029558 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20220929 MGI PMID:24316420 1322217 Mecom MDS1 and EVI1 complex locus gene MP:0031434 increased miscarriage rate IAGP N RGD:5509061 20220915 MGI PMID:17029558 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20161222 MGI PMID:26697887 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20161222 MGI PMID:26697887 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20161222 MGI PMID:26697887 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20161222 MGI PMID:26697887 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20161222 MGI PMID:26697887 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20161222 MGI PMID:26697887 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20161222 MGI PMID:26697887 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20161222 MGI PMID:26697887 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20161222 MGI PMID:26697887 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0005356 positive geotaxis IAGP N RGD:5509061 20161222 MGI PMID:26697887 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20161222 MGI PMID:26697887 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20161222 MGI PMID:26697887 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20161222 MGI PMID:26697887 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322219 Pitrm1 pitrilysin metallepetidase 1 gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20161222 MGI PMID:26697887 1322221 Cadm1 cell adhesion molecule 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:17130425 1322221 Cadm1 cell adhesion molecule 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16611999 1322221 Cadm1 cell adhesion molecule 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16612000 1322221 Cadm1 cell adhesion molecule 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22084409 1322221 Cadm1 cell adhesion molecule 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22084409 1322221 Cadm1 cell adhesion molecule 1 gene MP:0001391 abnormal tail movements IEA N RGD:5509061 20160804 MGI 1322221 Cadm1 cell adhesion molecule 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16382161 1322221 Cadm1 cell adhesion molecule 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16611999 1322221 Cadm1 cell adhesion molecule 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16612000 1322221 Cadm1 cell adhesion molecule 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22084409 1322221 Cadm1 cell adhesion molecule 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17130425 1322221 Cadm1 cell adhesion molecule 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16611999 1322221 Cadm1 cell adhesion molecule 1 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17130425 1322221 Cadm1 cell adhesion molecule 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16382161 1322221 Cadm1 cell adhesion molecule 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16611999 1322221 Cadm1 cell adhesion molecule 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16612000 1322221 Cadm1 cell adhesion molecule 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16612000 1322221 Cadm1 cell adhesion molecule 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16382161 1322221 Cadm1 cell adhesion molecule 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16611999 1322221 Cadm1 cell adhesion molecule 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16612000 1322221 Cadm1 cell adhesion molecule 1 gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141009 MGI PMID:24361012 1322221 Cadm1 cell adhesion molecule 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:22084409 1322221 Cadm1 cell adhesion molecule 1 gene MP:0004850 abnormal testis weight IAGP N RGD:5509061 20141003 MGI PMID:16382161 1322221 Cadm1 cell adhesion molecule 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16612000 1322221 Cadm1 cell adhesion molecule 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:16382161 1322221 Cadm1 cell adhesion molecule 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1322221 Cadm1 cell adhesion molecule 1 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22084409 1322221 Cadm1 cell adhesion molecule 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22084409 1322221 Cadm1 cell adhesion molecule 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16382161 1322221 Cadm1 cell adhesion molecule 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16611999 1322221 Cadm1 cell adhesion molecule 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16612000 1322221 Cadm1 cell adhesion molecule 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:16382161 1322221 Cadm1 cell adhesion molecule 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:18055550 1322221 Cadm1 cell adhesion molecule 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22084409 1322221 Cadm1 cell adhesion molecule 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22084409 1322221 Cadm1 cell adhesion molecule 1 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16382161 1322221 Cadm1 cell adhesion molecule 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17130425 1322221 Cadm1 cell adhesion molecule 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22084409 1322221 Cadm1 cell adhesion molecule 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:22084409 1322221 Cadm1 cell adhesion molecule 1 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:22084409 1322221 Cadm1 cell adhesion molecule 1 gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:22084409 1322221 Cadm1 cell adhesion molecule 1 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141009 MGI PMID:24361012 1322221 Cadm1 cell adhesion molecule 1 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:16612000 1322221 Cadm1 cell adhesion molecule 1 gene MP:0009839 multiflagellated sperm IAGP N RGD:5509061 20141003 MGI PMID:16612000 1322221 Cadm1 cell adhesion molecule 1 gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20141009 MGI PMID:24361012 1322223 Spmip6 sperm microtubule inner protein 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1322224 A2ml1 alpha-2-macroglobulin like 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1322224 A2ml1 alpha-2-macroglobulin like 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1322224 A2ml1 alpha-2-macroglobulin like 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201022 MGI 1322225 Pfn3 profilin 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0009325 necrospermia IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0030949 abnormal Golgi vesicle transport IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0031355 abnormal proacrosomal vesicle fusion IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322225 Pfn3 profilin 3 gene MP:0031374 abnormal manchette assembly IAGP N RGD:5509061 20220407 MGI PMID:34869336 1322229 Ift52 intraflagellar transport 52 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1322229 Ift52 intraflagellar transport 52 gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20201022 MGI 1322229 Ift52 intraflagellar transport 52 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1322229 Ift52 intraflagellar transport 52 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20201022 MGI 1322229 Ift52 intraflagellar transport 52 gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20201022 MGI 1322229 Ift52 intraflagellar transport 52 gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1322229 Ift52 intraflagellar transport 52 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1322229 Ift52 intraflagellar transport 52 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1322229 Ift52 intraflagellar transport 52 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20201022 MGI 1322229 Ift52 intraflagellar transport 52 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20201022 MGI 1322229 Ift52 intraflagellar transport 52 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1322229 Ift52 intraflagellar transport 52 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IEA N RGD:5509061 20111116 MGI 1322229 Ift52 intraflagellar transport 52 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322229 Ift52 intraflagellar transport 52 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1322232 C1qtnf4 C1q and tumor necrosis factor related protein 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1322232 C1qtnf4 C1q and tumor necrosis factor related protein 4 gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20210819 MGI PMID:33080044 1322232 C1qtnf4 C1q and tumor necrosis factor related protein 4 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20210819 MGI PMID:33080044 1322232 C1qtnf4 C1q and tumor necrosis factor related protein 4 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20210819 MGI PMID:33080044 1322232 C1qtnf4 C1q and tumor necrosis factor related protein 4 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20210819 MGI PMID:33080044 1322232 C1qtnf4 C1q and tumor necrosis factor related protein 4 gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20210819 MGI PMID:33080044 1322232 C1qtnf4 C1q and tumor necrosis factor related protein 4 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20210819 MGI PMID:33080044 1322232 C1qtnf4 C1q and tumor necrosis factor related protein 4 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210819 MGI PMID:33080044 1322233 Myo18a myosin XVIIIA gene MP:0000603 pale liver IEA N RGD:5509061 20210520 MGI 1322233 Myo18a myosin XVIIIA gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1322233 Myo18a myosin XVIIIA gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1322233 Myo18a myosin XVIIIA gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1322233 Myo18a myosin XVIIIA gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20191003 MGI PMID:30737279 1322233 Myo18a myosin XVIIIA gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20191003 MGI PMID:30737279 1322233 Myo18a myosin XVIIIA gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20160811 MGI 1322233 Myo18a myosin XVIIIA gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20160811 MGI 1322233 Myo18a myosin XVIIIA gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20191003 MGI PMID:30737279 1322233 Myo18a myosin XVIIIA gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20191003 MGI PMID:30737279 1322233 Myo18a myosin XVIIIA gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20191003 MGI PMID:30737279 1322233 Myo18a myosin XVIIIA gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20191003 MGI PMID:30737279 1322233 Myo18a myosin XVIIIA gene MP:0030566 abnormal A band morphology IAGP N RGD:5509061 20191003 MGI PMID:30737279 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210128 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20200402 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20160804 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0000322 increased granulocyte number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20160114 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0001258 decreased body length IEA N RGD:5509061 20200402 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210128 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20200402 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0003884 decreased macrophage cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0004974 decreased regulatory T cell number IEA N RGD:5509061 20201022 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0008039 increased NK T cell number IEA N RGD:5509061 20160804 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20160804 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0008124 decreased plasmacytoid dendritic cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0008127 decreased dendritic cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0008346 increased gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0009926 decreased transitional stage T2 B cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0010093 decreased circulating magnesium level IEA N RGD:5509061 20210128 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0010851 decreased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0012768 decreased KLRG1-positive NK cell number IEA N RGD:5509061 20160804 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0013155 decreased KLRG1+ CD8 alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0013427 increased memory-marker NK cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0013429 decreased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0013430 increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0013511 increased CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0013513 decreased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0013519 decreased CD4-positive NK T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0013522 decreased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0013667 increased immature NK cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0013672 decreased mature NK cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0013675 decreased Ly6C-positive mature NK cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0013679 increased Ly6C-positive NK T cell number IEA N RGD:5509061 20201231 MGI 1322235 Gmds GDP-mannose 4, 6-dehydratase gene MP:0013764 decreased T-helper cell number IEA N RGD:5509061 20201231 MGI 1322238 Cradd CASP2 and RIPK1 domain containing adaptor with death domain gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:16183742 1322238 Cradd CASP2 and RIPK1 domain containing adaptor with death domain gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16183742 1322238 Cradd CASP2 and RIPK1 domain containing adaptor with death domain gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15865046 1322240 Loxl3 lysyl oxidase-like 3 gene MP:0000088 short mandible IAGP N RGD:5509061 20160310 MGI PMID:26307084 1322240 Loxl3 lysyl oxidase-like 3 gene MP:0000098 abnormal vomer bone morphology IAGP N RGD:5509061 20160310 MGI PMID:26307084 1322240 Loxl3 lysyl oxidase-like 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20160310 MGI PMID:26307084 1322240 Loxl3 lysyl oxidase-like 3 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20160310 MGI PMID:26307084 1322240 Loxl3 lysyl oxidase-like 3 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20160310 MGI PMID:26307084 1322240 Loxl3 lysyl oxidase-like 3 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20160310 MGI PMID:26307084 1322240 Loxl3 lysyl oxidase-like 3 gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20160310 MGI PMID:26307084 1322240 Loxl3 lysyl oxidase-like 3 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20160310 MGI PMID:26307084 1322240 Loxl3 lysyl oxidase-like 3 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20160310 MGI PMID:26307084 1322240 Loxl3 lysyl oxidase-like 3 gene MP:0005227 abnormal vertebral body development IAGP N RGD:5509061 20160310 MGI PMID:26307084 1322240 Loxl3 lysyl oxidase-like 3 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20160310 MGI PMID:26307084 1322240 Loxl3 lysyl oxidase-like 3 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20160310 MGI PMID:26307084 1322240 Loxl3 lysyl oxidase-like 3 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20160310 MGI PMID:26307084 1322240 Loxl3 lysyl oxidase-like 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160310 MGI PMID:26307084 1322240 Loxl3 lysyl oxidase-like 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20160310 MGI PMID:26307084 1322244 Tbx2 T-box 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:22130515 1322244 Tbx2 T-box 2 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:22130515 1322244 Tbx2 T-box 2 gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:15459098 1322244 Tbx2 T-box 2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:15459098 1322244 Tbx2 T-box 2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19769959 1322244 Tbx2 T-box 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:15459098 1322244 Tbx2 T-box 2 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:15459098 1322244 Tbx2 T-box 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19769959 1322244 Tbx2 T-box 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20095052 1322244 Tbx2 T-box 2 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:15459098 1322244 Tbx2 T-box 2 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:15459098 1322244 Tbx2 T-box 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22130515 1322244 Tbx2 T-box 2 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:15459098 1322244 Tbx2 T-box 2 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:20095052 1322244 Tbx2 T-box 2 gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20141003 MGI PMID:15459098 1322244 Tbx2 T-box 2 gene MP:0009382 abnormal cardiac jelly morphology IAGP N RGD:5509061 20141003 MGI PMID:22130515 1322244 Tbx2 T-box 2 gene MP:0009744 postaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:20095052 1322244 Tbx2 T-box 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:19769959 1322244 Tbx2 T-box 2 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:15459098 1322244 Tbx2 T-box 2 gene MP:0010587 conotruncal ridge hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15459098 1322244 Tbx2 T-box 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19769959 1322244 Tbx2 T-box 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20095052 1322244 Tbx2 T-box 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15459098 1322244 Tbx2 T-box 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15459098 1322244 Tbx2 T-box 2 gene MP:0013917 persistent right 6th pharyngeal arch artery IAGP N RGD:5509061 20191219 MGI PMID:15459098 1322244 Tbx2 T-box 2 gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20220721 MGI PMID:19769959 1322244 Tbx2 T-box 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:19769959 1322244 Tbx2 T-box 2 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:19769959 1322246 Gramd2b GRAM domain containing 2B gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1322246 Gramd2b GRAM domain containing 2B gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230601 MGI 1322246 Gramd2b GRAM domain containing 2B gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1322246 Gramd2b GRAM domain containing 2B gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1322246 Gramd2b GRAM domain containing 2B gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1322246 Gramd2b GRAM domain containing 2B gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1322246 Gramd2b GRAM domain containing 2B gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1322246 Gramd2b GRAM domain containing 2B gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230601 MGI 1322246 Gramd2b GRAM domain containing 2B gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 1322246 Gramd2b GRAM domain containing 2B gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230601 MGI 1322249 Robo3 roundabout guidance receptor 3 gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20141003 MGI PMID:20680010 1322249 Robo3 roundabout guidance receptor 3 gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:20231872 1322249 Robo3 roundabout guidance receptor 3 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:15084255 1322249 Robo3 roundabout guidance receptor 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220519 MGI 1322249 Robo3 roundabout guidance receptor 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20231872 1322249 Robo3 roundabout guidance receptor 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20231872 1322249 Robo3 roundabout guidance receptor 3 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:20231872 1322249 Robo3 roundabout guidance receptor 3 gene MP:0001525 impaired balance IEA N RGD:5509061 20120105 MGI 1322249 Robo3 roundabout guidance receptor 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:20680010 1322249 Robo3 roundabout guidance receptor 3 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:20680010 1322249 Robo3 roundabout guidance receptor 3 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:20231872 1322249 Robo3 roundabout guidance receptor 3 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:20231872 1322249 Robo3 roundabout guidance receptor 3 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:20231872 1322249 Robo3 roundabout guidance receptor 3 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220519 MGI 1322249 Robo3 roundabout guidance receptor 3 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15084255 1322249 Robo3 roundabout guidance receptor 3 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20231872 1322249 Robo3 roundabout guidance receptor 3 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220519 MGI 1322249 Robo3 roundabout guidance receptor 3 gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20141003 MGI PMID:20231872 1322249 Robo3 roundabout guidance receptor 3 gene MP:0010745 abnormal pre-Botzinger complex morphology IAGP N RGD:5509061 20141003 MGI PMID:20680010 1322249 Robo3 roundabout guidance receptor 3 gene MP:0010746 abnormal pre-Botzinger complex physiology IAGP N RGD:5509061 20141003 MGI PMID:20680010 1322249 Robo3 roundabout guidance receptor 3 gene MP:0011042 abnormal horizontal vestibuloocular reflex IAGP N RGD:5509061 20141003 MGI PMID:20231872 1322249 Robo3 roundabout guidance receptor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20680010 1322249 Robo3 roundabout guidance receptor 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15084255 1322249 Robo3 roundabout guidance receptor 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1322249 Robo3 roundabout guidance receptor 3 gene MP:0021092 abnormal dorsal interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:18701067 1322256 Dysf dysferlin gene MP:0000604 amyloidosis IAGP N RGD:5509061 20210429 MGI PMID:30292141 1322256 Dysf dysferlin gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:21060153 1322256 Dysf dysferlin gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:10508505 1322256 Dysf dysferlin gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:10508505 1322256 Dysf dysferlin gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:12736685 1322256 Dysf dysferlin gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:22666441 1322256 Dysf dysferlin gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20160114 MGI PMID:25198651 1322256 Dysf dysferlin gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20210429 MGI PMID:30292141 1322256 Dysf dysferlin gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15254015 1322256 Dysf dysferlin gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20160114 MGI PMID:25198651 1322256 Dysf dysferlin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15254015 1322256 Dysf dysferlin gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20210429 MGI PMID:30292141 1322256 Dysf dysferlin gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20210429 MGI PMID:30292141 1322256 Dysf dysferlin gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15254015 1322256 Dysf dysferlin gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20160114 MGI PMID:25198651 1322256 Dysf dysferlin gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20161216 MGI PMID:21060153 1322256 Dysf dysferlin gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:12736685 1322256 Dysf dysferlin gene MP:0004262 abnormal physical strength IAGP N RGD:5509061 20141003 MGI PMID:15254015 1322256 Dysf dysferlin gene MP:0004510 myositis IAGP N RGD:5509061 20160114 MGI PMID:25198651 1322256 Dysf dysferlin gene MP:0004510 myositis IAGP N RGD:5509061 20161216 MGI PMID:21060153 1322256 Dysf dysferlin gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:15254015 1322256 Dysf dysferlin gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:12736685 1322256 Dysf dysferlin gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20160114 MGI PMID:25198651 1322256 Dysf dysferlin gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20161216 MGI PMID:21060153 1322256 Dysf dysferlin gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:12736685 1322256 Dysf dysferlin gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:15254015 1322256 Dysf dysferlin gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20160114 MGI PMID:25198651 1322256 Dysf dysferlin gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20161216 MGI PMID:21060153 1322256 Dysf dysferlin gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:12736685 1322256 Dysf dysferlin gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:15254015 1322256 Dysf dysferlin gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20160114 MGI PMID:25198651 1322256 Dysf dysferlin gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:12736685 1322256 Dysf dysferlin gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:15254015 1322256 Dysf dysferlin gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20160114 MGI PMID:25198651 1322256 Dysf dysferlin gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20210429 MGI PMID:30292141 1322256 Dysf dysferlin gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20160114 MGI PMID:25198651 1322256 Dysf dysferlin gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20161216 MGI PMID:21060153 1322256 Dysf dysferlin gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20210429 MGI PMID:30292141 1322256 Dysf dysferlin gene MP:0009420 skeletal muscle endomysial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15254015 1322256 Dysf dysferlin gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:12736685 1322256 Dysf dysferlin gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20161216 MGI PMID:21060153 1322256 Dysf dysferlin gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:12736685 1322256 Dysf dysferlin gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20231109 MGI PMID:36400788 1322258 Pum2 pumilio RNA-binding family member 2 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:17219433 1322258 Pum2 pumilio RNA-binding family member 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20231207 MGI 1322258 Pum2 pumilio RNA-binding family member 2 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20231207 MGI 1322258 Pum2 pumilio RNA-binding family member 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20231207 MGI 1322258 Pum2 pumilio RNA-binding family member 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17219433 1322258 Pum2 pumilio RNA-binding family member 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20231207 MGI 1322258 Pum2 pumilio RNA-binding family member 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1322260 Fam53c family with sequence similarity 53, member C gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1322261 Tkfc triokinase, FMN cyclase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1322261 Tkfc triokinase, FMN cyclase gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1322261 Tkfc triokinase, FMN cyclase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1322261 Tkfc triokinase, FMN cyclase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1322261 Tkfc triokinase, FMN cyclase gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1322261 Tkfc triokinase, FMN cyclase gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1322261 Tkfc triokinase, FMN cyclase gene MP:0001330 abnormal optic nerve morphology IEA N RGD:5509061 20230601 MGI 1322261 Tkfc triokinase, FMN cyclase gene MP:0001333 absent optic nerve IEA N RGD:5509061 20230601 MGI 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20180913 MGI PMID:29212046 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180913 MGI PMID:29212046 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20180913 MGI PMID:29212046 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20180913 MGI PMID:29212046 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20180913 MGI PMID:29212046 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20210128 MGI 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20180913 MGI PMID:29212046 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20180913 MGI PMID:29212046 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20180913 MGI PMID:29212046 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20180913 MGI PMID:29212046 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230601 MGI 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20180913 MGI PMID:29212046 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20180913 MGI PMID:29212046 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1322264 Arhgap21 Rho GTPase activating protein 21 gene MP:0020463 increased megakaryocyte progenitor cell number IAGP N RGD:5509061 20180913 MGI PMID:29212046 1322267 Tmod3 tropomodulin 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:24159174 1322267 Tmod3 tropomodulin 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:24159174 1322267 Tmod3 tropomodulin 3 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:24159174 1322267 Tmod3 tropomodulin 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:24159174 1322267 Tmod3 tropomodulin 3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24159174 1322267 Tmod3 tropomodulin 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:24159174 1322267 Tmod3 tropomodulin 3 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:24159174 1322267 Tmod3 tropomodulin 3 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:24159174 1322267 Tmod3 tropomodulin 3 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24159174 1322267 Tmod3 tropomodulin 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24159174 1322267 Tmod3 tropomodulin 3 gene MP:0011176 abnormal erythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:24159174 1322271 Cst9 cystatin 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15923608 1322271 Cst9 cystatin 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16427609 1322271 Cst9 cystatin 9 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1322271 Cst9 cystatin 9 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20170105 MGI 1322273 Ppp1r16b protein phosphatase 1, regulatory subunit 16B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17683113 1322275 Ethe1 ethylmalonic encephalopathy 1 gene MP:0000192 abnormal mineral level IAGP N RGD:5509061 20141003 MGI PMID:19136963 1322275 Ethe1 ethylmalonic encephalopathy 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19136963 1322275 Ethe1 ethylmalonic encephalopathy 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19136963 1322275 Ethe1 ethylmalonic encephalopathy 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19136963 1322275 Ethe1 ethylmalonic encephalopathy 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19136963 1322275 Ethe1 ethylmalonic encephalopathy 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:19136963 1322275 Ethe1 ethylmalonic encephalopathy 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:19136963 1322275 Ethe1 ethylmalonic encephalopathy 1 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 1322275 Ethe1 ethylmalonic encephalopathy 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19136963 1322275 Ethe1 ethylmalonic encephalopathy 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19136963 1322275 Ethe1 ethylmalonic encephalopathy 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1322275 Ethe1 ethylmalonic encephalopathy 1 gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:19136963 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0001785 edema IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0011321 abnormal peritubular capillary morphology IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0011444 abnormal renal water homeostasis IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0011454 abnormal glomerular endothelium fenestra morphology IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0011856 abnormal glomerular filtration barrier function IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322278 Zfyve21 zinc finger, FYVE domain containing 21 gene MP:0013285 abnormal renal filtration IAGP N RGD:5509061 20240829 MGI PMID:38797325 1322280 Crls1 cardiolipin synthase 1 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322280 Crls1 cardiolipin synthase 1 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322280 Crls1 cardiolipin synthase 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322280 Crls1 cardiolipin synthase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322280 Crls1 cardiolipin synthase 1 gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0014396 decreased fat cell mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:29861389 1322280 Crls1 cardiolipin synthase 1 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20210729 MGI PMID:29861389 1322282 Saxo1 stabilizer of axonemal microtubules 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1322282 Saxo1 stabilizer of axonemal microtubules 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1322282 Saxo1 stabilizer of axonemal microtubules 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210506 MGI PMID:32814578 1322282 Saxo1 stabilizer of axonemal microtubules 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20211021 MGI 1322282 Saxo1 stabilizer of axonemal microtubules 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1322282 Saxo1 stabilizer of axonemal microtubules 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0000585 kinked tail IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:10205062 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17267005 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23946405 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:14985318 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001304 cataract IAGP N RGD:5509061 20170126 MGI PMID:26978024 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11114194 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:12752778 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:16123450 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:3417421 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:11114194 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:11929848 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:12752778 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:15184660 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:16123450 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:17267005 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001326 retina degeneration IAGP N RGD:5509061 20220519 MGI PMID:33539865 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:12387789 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:23946405 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20170126 MGI PMID:26978024 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11114194 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001505 hunched posture IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14985318 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:16123450 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17267005 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:16123450 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:23946405 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20170126 MGI PMID:26978024 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0003099 retina detachment IAGP N RGD:5509061 20170126 MGI PMID:26978024 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8638127 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20220519 MGI PMID:33539865 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:5009246 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10205062 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11114194 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:864040 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23946405 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11980879 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23946405 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0005114 premature hair loss IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:11980879 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20170525 MGI PMID:26392540 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20220519 MGI PMID:33539865 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20170126 MGI PMID:26978024 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:3417421 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11980879 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17213800 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17267005 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23946405 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:8638127 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20141003 MGI PMID:16123450 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:12522242 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:18545654 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20160114 MGI PMID:25477496 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20220519 MGI PMID:33539865 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20170126 MGI PMID:26978024 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008259 abnormal optic disk morphology IAGP N RGD:5509061 20141003 MGI PMID:16123450 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:11114194 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:12387789 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:23946405 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:3417421 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17267005 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20141003 MGI PMID:14985318 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008454 absent retina rod cells IAGP N RGD:5509061 20141003 MGI PMID:11114194 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008454 absent retina rod cells IAGP N RGD:5509061 20141003 MGI PMID:16576828 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20220519 MGI PMID:33539865 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:12752778 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20220519 MGI PMID:33539865 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:12387789 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:16123450 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:3417421 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20220519 MGI PMID:33539865 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008517 thick retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:14985318 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:17267005 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:3005510 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:11980879 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20220519 MGI PMID:33539865 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008520 disorganized retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:11980879 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:11114194 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:3417421 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0008918 microgliosis IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0009274 buphthalmos IAGP N RGD:5509061 20170126 MGI PMID:26978024 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20160114 MGI PMID:25477496 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23946405 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20220519 MGI PMID:33539865 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0011279 decreased ear pigmentation IAGP N RGD:5509061 20170803 MGI PMID:864040 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0011831 abnormal visual contrast sensitivity IAGP N RGD:5509061 20151119 MGI PMID:22633808 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:3417421 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20220519 MGI PMID:33539865 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0013258 abnormal extracellular matrix morphology IAGP N RGD:5509061 20200514 MGI PMID:31754016 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0020442 serous retina detachment IAGP N RGD:5509061 20170907 MGI PMID:26978024 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:11114194 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:18545654 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20171012 MGI PMID:11114194 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0031139 abnormal retina artery morphology IAGP N RGD:5509061 20220519 MGI PMID:33539865 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:11929848 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:16123450 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:17213800 1322284 Pde6b phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:17267005 1322286 Gbp5 guanylate binding protein 5 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:22461501 1322286 Gbp5 guanylate binding protein 5 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1322286 Gbp5 guanylate binding protein 5 gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:22461501 1322286 Gbp5 guanylate binding protein 5 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:22461501 1322286 Gbp5 guanylate binding protein 5 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22461501 1322286 Gbp5 guanylate binding protein 5 gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:22461501 1322286 Gbp5 guanylate binding protein 5 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:22461501 1322288 Arid5a AT-rich interaction domain 5A gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:23676272 1322288 Arid5a AT-rich interaction domain 5A gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23676272 1322288 Arid5a AT-rich interaction domain 5A gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:23676272 1322288 Arid5a AT-rich interaction domain 5A gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:23676272 1322288 Arid5a AT-rich interaction domain 5A gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:23676272 1322291 Sbds SBDS ribosome maturation factor gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20305640 1322291 Sbds SBDS ribosome maturation factor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:21536732 1322291 Sbds SBDS ribosome maturation factor gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22510201 1322291 Sbds SBDS ribosome maturation factor gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20305640 1322291 Sbds SBDS ribosome maturation factor gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:21536732 1322291 Sbds SBDS ribosome maturation factor gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:16914746 1322291 Sbds SBDS ribosome maturation factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16914746 1322291 Sbds SBDS ribosome maturation factor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16914746 1322291 Sbds SBDS ribosome maturation factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22510201 1322291 Sbds SBDS ribosome maturation factor gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16914746 1322291 Sbds SBDS ribosome maturation factor gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:20305640 1322291 Sbds SBDS ribosome maturation factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16914746 1322291 Sbds SBDS ribosome maturation factor gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:20305640 1322291 Sbds SBDS ribosome maturation factor gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20305640 1322291 Sbds SBDS ribosome maturation factor gene MP:0003338 pancreas lipomatosis IAGP N RGD:5509061 20141003 MGI PMID:22510201 1322291 Sbds SBDS ribosome maturation factor gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:20305640 1322291 Sbds SBDS ribosome maturation factor gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:22510201 1322291 Sbds SBDS ribosome maturation factor gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20305640 1322291 Sbds SBDS ribosome maturation factor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20305640 1322291 Sbds SBDS ribosome maturation factor gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:20305640 1322291 Sbds SBDS ribosome maturation factor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22510201 1322291 Sbds SBDS ribosome maturation factor gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20305640 1322291 Sbds SBDS ribosome maturation factor gene MP:0008805 decreased circulating amylase level IAGP N RGD:5509061 20141003 MGI PMID:22510201 1322291 Sbds SBDS ribosome maturation factor gene MP:0009111 pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22510201 1322291 Sbds SBDS ribosome maturation factor gene MP:0009154 pancreatic acinar hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22510201 1322291 Sbds SBDS ribosome maturation factor gene MP:0009170 abnormal pancreatic islet size IAGP N RGD:5509061 20141003 MGI PMID:22510201 1322291 Sbds SBDS ribosome maturation factor gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21536732 1322291 Sbds SBDS ribosome maturation factor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21536732 1322291 Sbds SBDS ribosome maturation factor gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16914746 1322291 Sbds SBDS ribosome maturation factor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IEA N RGD:5509061 20230615 MGI 1322291 Sbds SBDS ribosome maturation factor gene MP:0011198 absent proamniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:16914746 1322291 Sbds SBDS ribosome maturation factor gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:16914746 1322291 Sbds SBDS ribosome maturation factor gene MP:0014242 abnormal ribosome biogenesis IEA N RGD:5509061 20230622 MGI 1322293 Gnb1l guanine nucleotide binding protein (G protein), beta polypeptide 1-like gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20231207 MGI 1322293 Gnb1l guanine nucleotide binding protein (G protein), beta polypeptide 1-like gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20231207 MGI 1322293 Gnb1l guanine nucleotide binding protein (G protein), beta polypeptide 1-like gene MP:0002743 glomerulonephritis IEA N RGD:5509061 20141003 MGI 1322293 Gnb1l guanine nucleotide binding protein (G protein), beta polypeptide 1-like gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20231207 MGI 1322293 Gnb1l guanine nucleotide binding protein (G protein), beta polypeptide 1-like gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20231207 MGI 1322293 Gnb1l guanine nucleotide binding protein (G protein), beta polypeptide 1-like gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20231207 MGI 1322293 Gnb1l guanine nucleotide binding protein (G protein), beta polypeptide 1-like gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20141003 MGI 1322293 Gnb1l guanine nucleotide binding protein (G protein), beta polypeptide 1-like gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20231207 MGI 1322293 Gnb1l guanine nucleotide binding protein (G protein), beta polypeptide 1-like gene MP:0008470 abnormal spleen B cell follicle morphology IEA N RGD:5509061 20141003 MGI 1322293 Gnb1l guanine nucleotide binding protein (G protein), beta polypeptide 1-like gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:16684884 1322293 Gnb1l guanine nucleotide binding protein (G protein), beta polypeptide 1-like gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 1322293 Gnb1l guanine nucleotide binding protein (G protein), beta polypeptide 1-like gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 1322293 Gnb1l guanine nucleotide binding protein (G protein), beta polypeptide 1-like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1322296 Tmprss15 transmembrane protease, serine 15 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1322296 Tmprss15 transmembrane protease, serine 15 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20160804 MGI 1322296 Tmprss15 transmembrane protease, serine 15 gene MP:0001258 decreased body length IEA N RGD:5509061 20160804 MGI 1322296 Tmprss15 transmembrane protease, serine 15 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1322296 Tmprss15 transmembrane protease, serine 15 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1322296 Tmprss15 transmembrane protease, serine 15 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20160804 MGI 1322296 Tmprss15 transmembrane protease, serine 15 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1322296 Tmprss15 transmembrane protease, serine 15 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1322296 Tmprss15 transmembrane protease, serine 15 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20160804 MGI 1322296 Tmprss15 transmembrane protease, serine 15 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160804 MGI 1322296 Tmprss15 transmembrane protease, serine 15 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20160804 MGI 1322296 Tmprss15 transmembrane protease, serine 15 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1322299 Rnf7 ring finger protein 7 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:22118770 1322299 Rnf7 ring finger protein 7 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22118770 1322299 Rnf7 ring finger protein 7 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:24210661 1322299 Rnf7 ring finger protein 7 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:24210661 1322299 Rnf7 ring finger protein 7 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:24210661 1322299 Rnf7 ring finger protein 7 gene MP:0000884 delaminated Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:24210661 1322299 Rnf7 ring finger protein 7 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:24210661 1322299 Rnf7 ring finger protein 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24210661 1322299 Rnf7 ring finger protein 7 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:22118770 1322299 Rnf7 ring finger protein 7 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:24210661 1322299 Rnf7 ring finger protein 7 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24430184 1322299 Rnf7 ring finger protein 7 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24430184 1322299 Rnf7 ring finger protein 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24430184 1322299 Rnf7 ring finger protein 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24210661 1322299 Rnf7 ring finger protein 7 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1322299 Rnf7 ring finger protein 7 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20160804 MGI 1322299 Rnf7 ring finger protein 7 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20160804 MGI 1322299 Rnf7 ring finger protein 7 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:22118770 1322299 Rnf7 ring finger protein 7 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22118770 1322299 Rnf7 ring finger protein 7 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:20638939 1322299 Rnf7 ring finger protein 7 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22118770 1322299 Rnf7 ring finger protein 7 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:20638939 1322299 Rnf7 ring finger protein 7 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22118770 1322299 Rnf7 ring finger protein 7 gene MP:0005316 abnormal response to tactile stimuli IEA N RGD:5509061 20141003 MGI 1322299 Rnf7 ring finger protein 7 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:22118770 1322299 Rnf7 ring finger protein 7 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:24210661 1322299 Rnf7 ring finger protein 7 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20638939 1322299 Rnf7 ring finger protein 7 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22118770 1322299 Rnf7 ring finger protein 7 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:24210661 1322299 Rnf7 ring finger protein 7 gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24210661 1322299 Rnf7 ring finger protein 7 gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24430184 1322299 Rnf7 ring finger protein 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22118770 1322299 Rnf7 ring finger protein 7 gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20141003 MGI PMID:22118770 1322299 Rnf7 ring finger protein 7 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:24210661 1322299 Rnf7 ring finger protein 7 gene MP:0013182 increased spinal cord apoptosis IAGP N RGD:5509061 20160428 MGI PMID:22118770 1322299 Rnf7 ring finger protein 7 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:22118770 1322299 Rnf7 ring finger protein 7 gene MP:0013551 decreased cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20161201 MGI PMID:24210661 1322304 Nup160 nucleoporin 160 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20210722 MGI PMID:32988961 1322304 Nup160 nucleoporin 160 gene MP:0011903 decreased hematopoietic stem cell proliferation IAGP N RGD:5509061 20210722 MGI PMID:32988961 1322307 Gins2 GINS complex subunit 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1322307 Gins2 GINS complex subunit 2 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 1322309 Eef1e1 eukaryotic translation elongation factor 1 epsilon 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15680327 1322309 Eef1e1 eukaryotic translation elongation factor 1 epsilon 1 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15680327 1322309 Eef1e1 eukaryotic translation elongation factor 1 epsilon 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15680327 1322309 Eef1e1 eukaryotic translation elongation factor 1 epsilon 1 gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15680327 1322309 Eef1e1 eukaryotic translation elongation factor 1 epsilon 1 gene MP:0009341 decreased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15680327 1322309 Eef1e1 eukaryotic translation elongation factor 1 epsilon 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15680327 1322309 Eef1e1 eukaryotic translation elongation factor 1 epsilon 1 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15680327 1322311 Brms1 breast cancer metastasis-suppressor 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1322311 Brms1 breast cancer metastasis-suppressor 1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 1322311 Brms1 breast cancer metastasis-suppressor 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1322311 Brms1 breast cancer metastasis-suppressor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1322313 Adck2 aarF domain containing kinase 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1322313 Adck2 aarF domain containing kinase 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0002804 abnormal motor learning IEA N RGD:5509061 20210520 MGI 1322313 Adck2 aarF domain containing kinase 2 gene MP:0003440 decreased glycerol level IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0003978 decreased circulating carnitine level IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 1322313 Adck2 aarF domain containing kinase 2 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0014174 decreased fatty acid beta-oxidation IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0030612 organic aciduria IAGP N RGD:5509061 20191128 MGI PMID:31480808 1322313 Adck2 aarF domain containing kinase 2 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:31480808 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20231207 MGI 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0010187 decreased T follicular helper cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20231207 MGI 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20231207 MGI 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0013436 increased CD8-positive, naive alpha-beta T cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0013705 decreased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0013771 decreased effector memory T-helper cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322316 Ctps1 cytidine 5'-triphosphate synthase 1 gene MP:0020154 impaired humoral immune response IAGP N RGD:5509061 20240627 MGI PMID:38438357 1322320 Tulp1 TUB like protein 1 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:11481257 1322320 Tulp1 TUB like protein 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20150129 MGI PMID:21052544 1322320 Tulp1 TUB like protein 1 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20210916 MGI PMID:22323461 1322320 Tulp1 TUB like protein 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:11481257 1322320 Tulp1 TUB like protein 1 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0005551 abnormal eye electrophysiology IEA N RGD:5509061 20220113 MGI 1322320 Tulp1 TUB like protein 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:11481257 1322320 Tulp1 TUB like protein 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20150129 MGI PMID:22183357 1322320 Tulp1 TUB like protein 1 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:11481257 1322320 Tulp1 TUB like protein 1 gene MP:0008583 absent photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20150129 MGI PMID:22183357 1322320 Tulp1 TUB like protein 1 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:11481257 1322320 Tulp1 TUB like protein 1 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220113 MGI 1322320 Tulp1 TUB like protein 1 gene MP:0010749 absent visual evoked potential IEA N RGD:5509061 20220113 MGI 1322320 Tulp1 TUB like protein 1 gene MP:0012671 retina spots IEA N RGD:5509061 20220113 MGI 1322320 Tulp1 TUB like protein 1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:10607826 1322320 Tulp1 TUB like protein 1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:10607826 1322321 Virma vir like m6A methyltransferase associated gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322321 Virma vir like m6A methyltransferase associated gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322321 Virma vir like m6A methyltransferase associated gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322321 Virma vir like m6A methyltransferase associated gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322324 Tekt2 tektin 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15340058 1322324 Tekt2 tektin 2 gene MP:0001947 abnormal mucociliary clearance IAGP N RGD:5509061 20141003 MGI PMID:15340058 1322324 Tekt2 tektin 2 gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15340058 1322324 Tekt2 tektin 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15340058 1322324 Tekt2 tektin 2 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:15340058 1322324 Tekt2 tektin 2 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20141003 MGI PMID:15340058 1322324 Tekt2 tektin 2 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:15340058 1322324 Tekt2 tektin 2 gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:15340058 1322328 Srsf10 serine and arginine-rich splicing factor 10 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19386262 1322328 Srsf10 serine and arginine-rich splicing factor 10 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:19386262 1322328 Srsf10 serine and arginine-rich splicing factor 10 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:19386262 1322328 Srsf10 serine and arginine-rich splicing factor 10 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:19386262 1322328 Srsf10 serine and arginine-rich splicing factor 10 gene MP:0004062 dilated heart right atrium IAGP N RGD:5509061 20141003 MGI PMID:19386262 1322328 Srsf10 serine and arginine-rich splicing factor 10 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19386262 1322328 Srsf10 serine and arginine-rich splicing factor 10 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:19386262 1322328 Srsf10 serine and arginine-rich splicing factor 10 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19386262 1322328 Srsf10 serine and arginine-rich splicing factor 10 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19386262 1322328 Srsf10 serine and arginine-rich splicing factor 10 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:19386262 1322328 Srsf10 serine and arginine-rich splicing factor 10 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19386262 1322328 Srsf10 serine and arginine-rich splicing factor 10 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19386262 1322328 Srsf10 serine and arginine-rich splicing factor 10 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19386262 1322329 Fezf2 Fez family zinc finger 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16284245 1322329 Fezf2 Fez family zinc finger 2 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:16971467 1322329 Fezf2 Fez family zinc finger 2 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:16971467 1322329 Fezf2 Fez family zinc finger 2 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:16971467 1322329 Fezf2 Fez family zinc finger 2 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:15188439 1322329 Fezf2 Fez family zinc finger 2 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:15188439 1322329 Fezf2 Fez family zinc finger 2 gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:15188439 1322329 Fezf2 Fez family zinc finger 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15188439 1322329 Fezf2 Fez family zinc finger 2 gene MP:0001432 abnormal food preference IAGP N RGD:5509061 20141003 MGI PMID:15188439 1322329 Fezf2 Fez family zinc finger 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15188439 1322329 Fezf2 Fez family zinc finger 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15188439 1322329 Fezf2 Fez family zinc finger 2 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:16284245 1322329 Fezf2 Fez family zinc finger 2 gene MP:0002243 abnormal vomeronasal organ morphology IAGP N RGD:5509061 20141003 MGI PMID:21452247 1322329 Fezf2 Fez family zinc finger 2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:16971467 1322329 Fezf2 Fez family zinc finger 2 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:21285371 1322329 Fezf2 Fez family zinc finger 2 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:22678282 1322329 Fezf2 Fez family zinc finger 2 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:16284245 1322329 Fezf2 Fez family zinc finger 2 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20160526 MGI PMID:24997765 1322329 Fezf2 Fez family zinc finger 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:16284245 1322329 Fezf2 Fez family zinc finger 2 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21452247 1322329 Fezf2 Fez family zinc finger 2 gene MP:0008228 increased anterior commissure size IAGP N RGD:5509061 20160526 MGI PMID:24997765 1322329 Fezf2 Fez family zinc finger 2 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:16971467 1322329 Fezf2 Fez family zinc finger 2 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16971467 1322329 Fezf2 Fez family zinc finger 2 gene MP:0011679 abnormal vomeronasal sensory neuron morphology IAGP N RGD:5509061 20150319 MGI PMID:21452247 1322329 Fezf2 Fez family zinc finger 2 gene MP:0012484 decreased corticospinal tract size IAGP N RGD:5509061 20160526 MGI PMID:24997765 1322329 Fezf2 Fez family zinc finger 2 gene MP:0013595 absent vomeronasal organ IAGP N RGD:5509061 20150319 MGI PMID:21452247 1322329 Fezf2 Fez family zinc finger 2 gene MP:0013597 small vomeronasal organ IAGP N RGD:5509061 20150319 MGI PMID:21452247 1322329 Fezf2 Fez family zinc finger 2 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:16971467 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19059699 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18416604 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15071178 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18500345 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19059699 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19201855 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15071178 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18416604 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:15071178 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:18416604 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:15071178 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:15071178 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19059699 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20150101 MGI PMID:24711413 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15071178 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18500345 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19059699 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18416604 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18684867 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10611229 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15071178 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19059699 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15071178 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18416604 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10611229 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18684867 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19059699 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8630375 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20150101 MGI PMID:24711413 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:8073287 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19059699 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19059699 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19201855 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18416604 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18500345 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19059699 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19201855 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20643340 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:8073287 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:8630375 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20150101 MGI PMID:24711413 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20210304 MGI PMID:25636339 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:18684867 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:8630375 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20210304 MGI PMID:25636339 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18684867 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18416604 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:15071178 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:18684867 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:19059699 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20150101 MGI PMID:24711413 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:19059699 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20150101 MGI PMID:24711413 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0008253 absent megakaryocytes IAGP N RGD:5509061 20141003 MGI PMID:8073287 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0008253 absent megakaryocytes IAGP N RGD:5509061 20141003 MGI PMID:8630375 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18684867 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20150101 MGI PMID:24711413 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19059699 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:15071178 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19059699 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20150101 MGI PMID:24711413 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:20643340 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:19059699 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15071178 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18416604 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20150101 MGI PMID:24711413 1322331 Mpl myeloproliferative leukemia virus oncogene gene MP:0014348 decreased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:15071178 1322334 Recql RecQ protein-like gene MP:0003701 elevated level of mitotic sister chromatid exchange IAGP N RGD:5509061 20141003 MGI PMID:17158923 1322334 Recql RecQ protein-like gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17158923 1322334 Recql RecQ protein-like gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:17158923 1322334 Recql RecQ protein-like gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:17158923 1322334 Recql RecQ protein-like gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:17158923 1322338 Poldip3 polymerase (DNA-directed), delta interacting protein 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1322338 Poldip3 polymerase (DNA-directed), delta interacting protein 3 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20240523 MGI 1322341 Psd2 pleckstrin and Sec7 domain containing 2 gene MP:0020360 abnormal asymmetric synapse morphology IAGP N RGD:5509061 20190919 MGI PMID:31095630 1322342 Klhl29 kelch-like 29 gene MP:0002626 increased heart rate IEA N RGD:5509061 20210128 MGI 1322342 Klhl29 kelch-like 29 gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20210128 MGI 1322342 Klhl29 kelch-like 29 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20210128 MGI 1322342 Klhl29 kelch-like 29 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20211021 MGI 1322342 Klhl29 kelch-like 29 gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20210128 MGI 1322342 Klhl29 kelch-like 29 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1322342 Klhl29 kelch-like 29 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 1322346 Lgi3 leucine-rich repeat LGI family, member 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1322346 Lgi3 leucine-rich repeat LGI family, member 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1322346 Lgi3 leucine-rich repeat LGI family, member 3 gene MP:0000745 tremors IAGP N RGD:5509061 20230330 MGI PMID:36828548 1322346 Lgi3 leucine-rich repeat LGI family, member 3 gene MP:0001200 thick skin IEA N RGD:5509061 20210128 MGI 1322346 Lgi3 leucine-rich repeat LGI family, member 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230330 MGI PMID:36828548 1322346 Lgi3 leucine-rich repeat LGI family, member 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1322346 Lgi3 leucine-rich repeat LGI family, member 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1322346 Lgi3 leucine-rich repeat LGI family, member 3 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20230330 MGI PMID:36828548 1322346 Lgi3 leucine-rich repeat LGI family, member 3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1322346 Lgi3 leucine-rich repeat LGI family, member 3 gene MP:0010737 abnormal juxtaparanode morphology IAGP N RGD:5509061 20220908 MGI PMID:35948005 1322346 Lgi3 leucine-rich repeat LGI family, member 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20230330 MGI PMID:36828548 1322349 Ndufs5 NADH:ubiquinone oxidoreductase core subunit S5 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230601 MGI 1322349 Ndufs5 NADH:ubiquinone oxidoreductase core subunit S5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1322351 Atp6v1c1 ATPase, H+ transporting, lysosomal V1 subunit C1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20201022 MGI 1322351 Atp6v1c1 ATPase, H+ transporting, lysosomal V1 subunit C1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20221215 MGI 1322351 Atp6v1c1 ATPase, H+ transporting, lysosomal V1 subunit C1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20181227 MGI 1322351 Atp6v1c1 ATPase, H+ transporting, lysosomal V1 subunit C1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20170105 MGI 1322351 Atp6v1c1 ATPase, H+ transporting, lysosomal V1 subunit C1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1322351 Atp6v1c1 ATPase, H+ transporting, lysosomal V1 subunit C1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1322351 Atp6v1c1 ATPase, H+ transporting, lysosomal V1 subunit C1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0000433 microcephaly IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0000774 decreased brain size IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0000852 small cerebellum IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0010059 olfactory bulb hypoplasia IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0013551 decreased cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322352 Chmp1a charged multivesicular body protein 1A gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20210415 MGI PMID:30044992 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17571162 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:16166380 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:17881575 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17881575 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:17881575 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0001341 absent eyelids IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:17881575 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:17881575 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15821749 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17571162 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12808090 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15821749 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:12808090 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15821749 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15821749 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15821749 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17571162 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15821749 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:16166380 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:17881575 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0003153 early eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0003359 hypaxial muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0003359 hypaxial muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16166380 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17881575 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:17571162 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17571162 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:17571162 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:17571162 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:17881575 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:17571162 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17571162 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15821749 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0005439 decreased glycogen level IAGP N RGD:5509061 20141003 MGI PMID:15821749 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15821749 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:17571162 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0008816 petechiae IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:17881575 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:17881575 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20141003 MGI PMID:16166380 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:17571162 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17923692 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17923692 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10779359 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808090 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17881575 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17881575 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:17881575 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0011527 disorganized placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0011527 disorganized placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:17881575 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0012185 abnormal muscle precursor cell morphology IAGP N RGD:5509061 20190725 MGI PMID:17881575 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20141003 MGI PMID:10995442 1322355 Gab1 growth factor receptor bound protein 2-associated protein 1 gene MP:0030208 abnormal intrinsic tongue muscle morphology IAGP N RGD:5509061 20171109 MGI PMID:16166380 1322360 Peg3 paternally expressed 3 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:10195900 1322360 Peg3 paternally expressed 3 gene MP:0001147 small testis IAGP N RGD:5509061 20141218 MGI PMID:24391757 1322360 Peg3 paternally expressed 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22394678 1322360 Peg3 paternally expressed 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10195900 1322360 Peg3 paternally expressed 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22394678 1322360 Peg3 paternally expressed 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141218 MGI PMID:24391757 1322360 Peg3 paternally expressed 3 gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:10195900 1322360 Peg3 paternally expressed 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141218 MGI PMID:24391757 1322360 Peg3 paternally expressed 3 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:10195900 1322360 Peg3 paternally expressed 3 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:22394678 1322360 Peg3 paternally expressed 3 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141218 MGI PMID:24391757 1322360 Peg3 paternally expressed 3 gene MP:0009326 absent maternal crouching IAGP N RGD:5509061 20141003 MGI PMID:10195900 1322360 Peg3 paternally expressed 3 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141218 MGI PMID:24391757 1322360 Peg3 paternally expressed 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141218 MGI PMID:24391757 1322360 Peg3 paternally expressed 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22394678 1322362 Stoml3 stomatin (Epb7.2)-like 3 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:17167420 1322362 Stoml3 stomatin (Epb7.2)-like 3 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:17167420 1322362 Stoml3 stomatin (Epb7.2)-like 3 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:17167420 1322364 Tedc1 tubulin epsilon and delta complex 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20190502 MGI 1322364 Tedc1 tubulin epsilon and delta complex 1 gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20190502 MGI 1322364 Tedc1 tubulin epsilon and delta complex 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1322364 Tedc1 tubulin epsilon and delta complex 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 1322364 Tedc1 tubulin epsilon and delta complex 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1322364 Tedc1 tubulin epsilon and delta complex 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1322364 Tedc1 tubulin epsilon and delta complex 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1322364 Tedc1 tubulin epsilon and delta complex 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20201022 MGI 1322364 Tedc1 tubulin epsilon and delta complex 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1322364 Tedc1 tubulin epsilon and delta complex 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1322366 Kbtbd13 kelch repeat and BTB (POZ) domain containing 13 gene MP:0001260 increased body weight IAGP N RGD:5509061 20201105 MGI PMID:31671076 1322366 Kbtbd13 kelch repeat and BTB (POZ) domain containing 13 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201105 MGI PMID:31671076 1322366 Kbtbd13 kelch repeat and BTB (POZ) domain containing 13 gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20201105 MGI PMID:31671076 1322366 Kbtbd13 kelch repeat and BTB (POZ) domain containing 13 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20201105 MGI PMID:31671076 1322366 Kbtbd13 kelch repeat and BTB (POZ) domain containing 13 gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20201105 MGI PMID:31671076 1322366 Kbtbd13 kelch repeat and BTB (POZ) domain containing 13 gene MP:0009425 increased soleus weight IAGP N RGD:5509061 20201105 MGI PMID:31671076 1322366 Kbtbd13 kelch repeat and BTB (POZ) domain containing 13 gene MP:0009426 decreased soleus weight IAGP N RGD:5509061 20201105 MGI PMID:31671076 1322366 Kbtbd13 kelch repeat and BTB (POZ) domain containing 13 gene MP:0010226 increased quadriceps weight IAGP N RGD:5509061 20201105 MGI PMID:31671076 1322366 Kbtbd13 kelch repeat and BTB (POZ) domain containing 13 gene MP:0012059 thick diaphragm muscle IAGP N RGD:5509061 20201105 MGI PMID:31671076 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15044845 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20171228 MGI PMID:20057387 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20171228 MGI PMID:20057387 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20667915 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21214893 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22991445 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20141003 MGI PMID:15917450 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20141003 MGI PMID:20667915 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:20667915 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:22991445 1322368 Emx2 empty spiracles homeobox 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0001329 retina hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15044845 1322368 Emx2 empty spiracles homeobox 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 1322368 Emx2 empty spiracles homeobox 2 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22991445 1322368 Emx2 empty spiracles homeobox 2 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 1322368 Emx2 empty spiracles homeobox 2 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0002623 abnormal vestibular hair cell morphology IAGP N RGD:5509061 20240822 MGI PMID:37144879 1322368 Emx2 empty spiracles homeobox 2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:21214893 1322368 Emx2 empty spiracles homeobox 2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:15044845 1322368 Emx2 empty spiracles homeobox 2 gene MP:0003005 abnormal hippocampal fimbria morphology IAGP N RGD:5509061 20141003 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0003006 abnormal hippocampal fornix morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22991445 1322368 Emx2 empty spiracles homeobox 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:20667915 1322368 Emx2 empty spiracles homeobox 2 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:22991445 1322368 Emx2 empty spiracles homeobox 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21214893 1322368 Emx2 empty spiracles homeobox 2 gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0003558 absent uterus IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0003575 absent oviduct IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0003578 absent ovary IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:21214893 1322368 Emx2 empty spiracles homeobox 2 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:22991445 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004171 abnormal pallium development IAGP N RGD:5509061 20141003 MGI PMID:20667915 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20667915 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004318 absent incus IAGP N RGD:5509061 20141003 MGI PMID:15044845 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004318 absent incus IAGP N RGD:5509061 20141003 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20171228 MGI PMID:20057387 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15044845 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15044845 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20171228 MGI PMID:20057387 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:15044845 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004729 absent efferent ductules of testis IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004739 conductive hearing loss IEA N RGD:5509061 20141003 MGI 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004740 sensorineural hearing loss IEA N RGD:5509061 20141003 MGI 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004750 syndromic hearing loss IEA N RGD:5509061 20141003 MGI 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004767 increased cochlear nerve compound action potential IAGP N RGD:5509061 20171228 MGI PMID:20057387 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:22991445 1322368 Emx2 empty spiracles homeobox 2 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:22991445 1322368 Emx2 empty spiracles homeobox 2 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15044845 1322368 Emx2 empty spiracles homeobox 2 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20171228 MGI PMID:20057387 1322368 Emx2 empty spiracles homeobox 2 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20171228 MGI PMID:20057387 1322368 Emx2 empty spiracles homeobox 2 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20171228 MGI PMID:20057387 1322368 Emx2 empty spiracles homeobox 2 gene MP:0005644 agonadal IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 1322368 Emx2 empty spiracles homeobox 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20171228 MGI PMID:20057387 1322368 Emx2 empty spiracles homeobox 2 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:15044845 1322368 Emx2 empty spiracles homeobox 2 gene MP:0006415 absent testes IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0006425 absent Mullerian ducts IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0008262 abnormal hippocampus region morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22991445 1322368 Emx2 empty spiracles homeobox 2 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:15917450 1322368 Emx2 empty spiracles homeobox 2 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20161103 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22991445 1322368 Emx2 empty spiracles homeobox 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22991445 1322368 Emx2 empty spiracles homeobox 2 gene MP:0009048 enlarged tectum IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0009072 absent cranial vagina IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0009074 Wolffian duct degeneration IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0009206 absent internal male genitalia IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0009210 absent internal female genitalia IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0009324 absent hippocampal fimbria IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0009324 absent hippocampal fimbria IAGP N RGD:5509061 20141003 MGI PMID:20667915 1322368 Emx2 empty spiracles homeobox 2 gene MP:0009637 abnormal pretectal region morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0009637 abnormal pretectal region morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 1322368 Emx2 empty spiracles homeobox 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:22991445 1322368 Emx2 empty spiracles homeobox 2 gene MP:0009951 abnormal olfactory bulb mitral cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0010893 abnormal posterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22991445 1322368 Emx2 empty spiracles homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15044845 1322368 Emx2 empty spiracles homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21214893 1322368 Emx2 empty spiracles homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0011412 gonadal ridge hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0011457 abnormal metanephric ureteric bud development IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0011760 abnormal ureteric bud tip morphology IAGP N RGD:5509061 20141003 MGI PMID:9165114 1322368 Emx2 empty spiracles homeobox 2 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:11493561 1322368 Emx2 empty spiracles homeobox 2 gene MP:0012517 absent diencephalon IAGP N RGD:5509061 20141003 MGI PMID:15201223 1322368 Emx2 empty spiracles homeobox 2 gene MP:0012517 absent diencephalon IAGP N RGD:5509061 20141003 MGI PMID:15917450 1322368 Emx2 empty spiracles homeobox 2 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:15917450 1322368 Emx2 empty spiracles homeobox 2 gene MP:0020545 decreased hippocampal fornix size IAGP N RGD:5509061 20180301 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0030108 abnormal incudostapedial joint morphology IAGP N RGD:5509061 20171005 MGI PMID:15044845 1322368 Emx2 empty spiracles homeobox 2 gene MP:0030109 abnormal incudomalleolar joint morphology IAGP N RGD:5509061 20171005 MGI PMID:9012509 1322368 Emx2 empty spiracles homeobox 2 gene MP:0030109 abnormal incudomalleolar joint morphology IAGP N RGD:5509061 20171207 MGI PMID:15044845 1322368 Emx2 empty spiracles homeobox 2 gene MP:0030396 abnormal incus long process morphology IAGP N RGD:5509061 20171207 MGI PMID:15044845 1322368 Emx2 empty spiracles homeobox 2 gene MP:0030398 absent incus lenticular process IAGP N RGD:5509061 20171207 MGI PMID:15044845 1322368 Emx2 empty spiracles homeobox 2 gene MP:0030402 abnormal stapes head morphology IAGP N RGD:5509061 20171207 MGI PMID:15044845 1322373 Ctr9 CTR9 homolog, Paf1/RNA polymerase II complex component gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1322373 Ctr9 CTR9 homolog, Paf1/RNA polymerase II complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322373 Ctr9 CTR9 homolog, Paf1/RNA polymerase II complex component gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1322373 Ctr9 CTR9 homolog, Paf1/RNA polymerase II complex component gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000026 abnormal inner ear morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000079 abnormal basioccipital bone morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000106 abnormal basisphenoid bone morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000111 cleft palate IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000141 abnormal vertebral body morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20150430 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0000297 abnormal atrioventricular cushion morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0000562 polydactyly IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000632 abnormal pineal gland morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0000690 absent spleen IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0000819 abnormal olfactory bulb morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0000897 abnormal midbrain morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0000964 small dorsal root ganglion IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0001014 absent superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0001062 absent oculomotor nerve IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0001075 abnormal accessory nerve morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322375 Rpgrip1l Rpgrip1-like gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0002237 abnormal nasal cavity morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0002239 abnormal nasal septum morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0003056 abnormal hyoid bone morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0003327 liver cyst IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0003584 bifid ureter IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0003755 abnormal palate morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0003888 liver hemorrhage IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0004110 transposition of great arteries IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0004158 right aortic arch IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0004181 abnormal carotid artery morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0004259 small placenta IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322375 Rpgrip1l Rpgrip1-like gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0004574 broad limb buds IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0004668 absent vertebral body IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0004950 abnormal brain vasculature morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0005157 holoprosencephaly IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0005358 abnormal incisor morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0006065 abnormal heart position or orientation IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0008129 absent brain internal capsule IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0008320 absent adenohypophysis IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0008461 left atrial isomerism IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322375 Rpgrip1l Rpgrip1-like gene MP:0008923 thoracoschisis IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0009526 absent sublingual gland IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0009570 abnormal right lung morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0009771 absent optic chiasm IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0009907 decreased tongue size IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0010403 atrial septal defect IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0010406 common atrium IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20150917 MGI PMID:23469020 1322375 Rpgrip1l Rpgrip1-like gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20150917 MGI PMID:23469020 1322375 Rpgrip1l Rpgrip1-like gene MP:0010427 double outlet left ventricle IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0010431 atrial situs inversus IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0010440 anomalous pulmonary venous connection IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0010490 abnormal inferior vena cava valve morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0010572 persistent right dorsal aorta IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17553904 1322375 Rpgrip1l Rpgrip1-like gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322375 Rpgrip1l Rpgrip1-like gene MP:0011250 abdominal situs ambiguus IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0011759 absent Rathke's pouch IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0012730 abnormal internal carotid artery morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013186 abnormal basilar artery morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013247 placenta necrosis IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322375 Rpgrip1l Rpgrip1-like gene MP:0013349 small Rathke's pouch IAGP N RGD:5509061 20141218 MGI PMID:17558409 1322375 Rpgrip1l Rpgrip1-like gene MP:0013828 thin facial nerve IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013830 abnormal intrathoracic topology of vagus nerve IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013852 abnormal Mullerian duct topology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013853 abnormal hepatic portal vein formation IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013858 abnormal azygos vein topology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013861 abnormal pancreas topology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013867 abnormal ventral pancreas morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013878 abnormal ductus venosus valve topology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013914 absent intracranial segment of vertebral artery IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013917 persistent right 6th pharyngeal arch artery IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013928 thin motoric part of trigeminal nerve IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013952 retroesophageal left subclavian artery IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013970 absent connection between subcutaneous lymph vessels and lymph sac IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013975 abnormal coronary sinus connection IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013977 symmetric azygos veins IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013979 abnormal subclavian artery origin IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013982 inverse situs of great intrathoracic arteries IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013985 abnormal umbilical vein topology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013987 absent intrahepatic inferior vena cava segment IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013996 abnormal vertebral artery origin IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013997 abnormal internal carotid artery topology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013998 absent canalicular internal carotid artery segment IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0013999 absent parasellar internal carotid artery IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0014000 anastomosis between internal carotid artery and basilar artery IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0014012 abnormal cranial blood vasculature morphology IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0014023 abnormal intestine placement IEA N RGD:5509061 20170504 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0020485 abnormal inferior vena cava topology IEA N RGD:5509061 20180628 MGI 1322375 Rpgrip1l Rpgrip1-like gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:29539633 1322376 Slc51a solute carrier family 51, alpha subunit gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:18292224 1322376 Slc51a solute carrier family 51, alpha subunit gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17650074 1322376 Slc51a solute carrier family 51, alpha subunit gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18292224 1322376 Slc51a solute carrier family 51, alpha subunit gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18292224 1322376 Slc51a solute carrier family 51, alpha subunit gene MP:0003947 abnormal cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18292224 1322376 Slc51a solute carrier family 51, alpha subunit gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:18292224 1322376 Slc51a solute carrier family 51, alpha subunit gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18292224 1322376 Slc51a solute carrier family 51, alpha subunit gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18292224 1322376 Slc51a solute carrier family 51, alpha subunit gene MP:0014480 increased feces cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:18292224 1322378 Cda cytidine deaminase gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20230406 MGI PMID:36496104 1322378 Cda cytidine deaminase gene MP:0003701 elevated level of mitotic sister chromatid exchange IAGP N RGD:5509061 20230406 MGI PMID:36496104 1322378 Cda cytidine deaminase gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20230406 MGI PMID:36496104 1322378 Cda cytidine deaminase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20230406 MGI PMID:36496104 1322378 Cda cytidine deaminase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20230406 MGI PMID:36496104 1322378 Cda cytidine deaminase gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20230406 MGI PMID:36496104 1322381 Ooep oocyte expressed protein gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18804437 1322381 Ooep oocyte expressed protein gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18804437 1322381 Ooep oocyte expressed protein gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20590823 1322381 Ooep oocyte expressed protein gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20200423 MGI PMID:25208553 1322381 Ooep oocyte expressed protein gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:18804437 1322381 Ooep oocyte expressed protein gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:20590823 1322381 Ooep oocyte expressed protein gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20200423 MGI PMID:25208553 1322381 Ooep oocyte expressed protein gene MP:0020850 abnormal microtubule cytoskeleton morphology IAGP N RGD:5509061 20200423 MGI PMID:25208553 1322384 Arid2 AT-rich interaction domain 2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20160324 MGI PMID:25299188 1322384 Arid2 AT-rich interaction domain 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20160324 MGI PMID:25299188 1322384 Arid2 AT-rich interaction domain 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20160324 MGI PMID:25299188 1322384 Arid2 AT-rich interaction domain 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160324 MGI PMID:25299188 1322384 Arid2 AT-rich interaction domain 2 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20160324 MGI PMID:25299188 1322384 Arid2 AT-rich interaction domain 2 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20160324 MGI PMID:25299188 1322384 Arid2 AT-rich interaction domain 2 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20160324 MGI PMID:25299188 1322384 Arid2 AT-rich interaction domain 2 gene MP:0010419 inlet ventricular septal defect IAGP N RGD:5509061 20160324 MGI PMID:25299188 1322384 Arid2 AT-rich interaction domain 2 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20160324 MGI PMID:25299188 1322384 Arid2 AT-rich interaction domain 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160324 MGI PMID:25299188 1322384 Arid2 AT-rich interaction domain 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322384 Arid2 AT-rich interaction domain 2 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20160324 MGI PMID:25299188 1322384 Arid2 AT-rich interaction domain 2 gene MP:0013848 subcutaneous edema IAGP N RGD:5509061 20160324 MGI PMID:25299188 1322386 Olfml3 olfactomedin-like 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16172977 1322399 Strap serine/threonine kinase receptor associated protein gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14981515 1322399 Strap serine/threonine kinase receptor associated protein gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:14981515 1322399 Strap serine/threonine kinase receptor associated protein gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:14981515 1322399 Strap serine/threonine kinase receptor associated protein gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:14981515 1322399 Strap serine/threonine kinase receptor associated protein gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:14981515 1322399 Strap serine/threonine kinase receptor associated protein gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20181206 MGI PMID:28827371 1322399 Strap serine/threonine kinase receptor associated protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14981515 1322401 Ap3s1 adaptor-related protein complex 3, sigma 1 subunit gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1322401 Ap3s1 adaptor-related protein complex 3, sigma 1 subunit gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:16980352 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12447442 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16461338 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15690042 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12447442 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15690042 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:12447441 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:12447441 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12447442 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:18492657 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0008555 abnormal interferon secretion IEA N RGD:5509061 20111116 MGI 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0008561 decreased tumor necrosis factor secretion IEA N RGD:5509061 20111116 MGI 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21148800 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:16461338 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:16461338 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:21148800 1322403 Tirap toll-interleukin 1 receptor (TIR) domain-containing adaptor protein gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15690042 1322404 Unc79 unc-79 homolog gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:16807365 1322404 Unc79 unc-79 homolog gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:20714347 1322404 Unc79 unc-79 homolog gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16807365 1322404 Unc79 unc-79 homolog gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20714347 1322404 Unc79 unc-79 homolog gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20714347 1322404 Unc79 unc-79 homolog gene MP:0001987 alcohol preference IAGP N RGD:5509061 20141003 MGI PMID:20714347 1322404 Unc79 unc-79 homolog gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20714347 1322404 Unc79 unc-79 homolog gene MP:0002849 abnormal saccharin consumption IAGP N RGD:5509061 20141003 MGI PMID:20714347 1322404 Unc79 unc-79 homolog gene MP:0002850 saccharin preference IAGP N RGD:5509061 20141003 MGI PMID:20714347 1322404 Unc79 unc-79 homolog gene MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:20714347 1322404 Unc79 unc-79 homolog gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:16807365 1322404 Unc79 unc-79 homolog gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:16807365 1322404 Unc79 unc-79 homolog gene MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:20714347 1322404 Unc79 unc-79 homolog gene MP:0009778 impaired behavioral response to anesthetic IAGP N RGD:5509061 20141003 MGI PMID:20714347 1322404 Unc79 unc-79 homolog gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20714347 1322404 Unc79 unc-79 homolog gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16807365 1322404 Unc79 unc-79 homolog gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16807365 1322404 Unc79 unc-79 homolog gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:20714347 1322404 Unc79 unc-79 homolog gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:16436185 1322407 Prdm13 PR domain containing 13 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 1322407 Prdm13 PR domain containing 13 gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20160728 MGI PMID:25995483 1322407 Prdm13 PR domain containing 13 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1322407 Prdm13 PR domain containing 13 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20231207 MGI 1322407 Prdm13 PR domain containing 13 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20160728 MGI PMID:25995483 1322407 Prdm13 PR domain containing 13 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20160728 MGI PMID:25995483 1322407 Prdm13 PR domain containing 13 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20160728 MGI PMID:25995483 1322407 Prdm13 PR domain containing 13 gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20160728 MGI PMID:25995483 1322407 Prdm13 PR domain containing 13 gene MP:0011831 abnormal visual contrast sensitivity IAGP N RGD:5509061 20160728 MGI PMID:25995483 1322409 Med17 mediator complex subunit 17 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1322409 Med17 mediator complex subunit 17 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1322409 Med17 mediator complex subunit 17 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1322411 Ell elongation factor RNA polymerase II gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11118326 1322414 Slc47a1 solute carrier family 47, member 1 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20181227 MGI 1322414 Slc47a1 solute carrier family 47, member 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:21991918 1322414 Slc47a1 solute carrier family 47, member 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:21991918 1322414 Slc47a1 solute carrier family 47, member 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201231 MGI 1322414 Slc47a1 solute carrier family 47, member 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:19332510 1322414 Slc47a1 solute carrier family 47, member 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:19332510 1322414 Slc47a1 solute carrier family 47, member 1 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20201022 MGI 1322414 Slc47a1 solute carrier family 47, member 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21991918 1322414 Slc47a1 solute carrier family 47, member 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:19332510 1322414 Slc47a1 solute carrier family 47, member 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:21991918 1322414 Slc47a1 solute carrier family 47, member 1 gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:21991918 1322419 Ttc39a tetratricopeptide repeat domain 39A gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 1322419 Ttc39a tetratricopeptide repeat domain 39A gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1322419 Ttc39a tetratricopeptide repeat domain 39A gene MP:0002833 increased heart weight IEA N RGD:5509061 20181227 MGI 1322419 Ttc39a tetratricopeptide repeat domain 39A gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 1322421 Gcm2 glial cells missing homolog 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10910362 1322421 Gcm2 glial cells missing homolog 2 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:10910362 1322421 Gcm2 glial cells missing homolog 2 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:12122115 1322421 Gcm2 glial cells missing homolog 2 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141009 MGI PMID:24736975 1322421 Gcm2 glial cells missing homolog 2 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:10910362 1322421 Gcm2 glial cells missing homolog 2 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:10910362 1322421 Gcm2 glial cells missing homolog 2 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:17382312 1322421 Gcm2 glial cells missing homolog 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:21765423 1322421 Gcm2 glial cells missing homolog 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:21765423 1322421 Gcm2 glial cells missing homolog 2 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141009 MGI PMID:24736975 1322421 Gcm2 glial cells missing homolog 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141009 MGI PMID:24736975 1322421 Gcm2 glial cells missing homolog 2 gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20141009 MGI PMID:24736975 1322421 Gcm2 glial cells missing homolog 2 gene MP:0003433 decreased activity of parathyroid IAGP N RGD:5509061 20141003 MGI PMID:10910362 1322421 Gcm2 glial cells missing homolog 2 gene MP:0003494 parathyroid hypoplasia IAGP N RGD:5509061 20141009 MGI PMID:24736975 1322421 Gcm2 glial cells missing homolog 2 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:10910362 1322421 Gcm2 glial cells missing homolog 2 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:10910362 1322421 Gcm2 glial cells missing homolog 2 gene MP:0006339 abnormal third pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:17382312 1322421 Gcm2 glial cells missing homolog 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10910362 1322421 Gcm2 glial cells missing homolog 2 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21765423 1322421 Gcm2 glial cells missing homolog 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21765423 1322421 Gcm2 glial cells missing homolog 2 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141009 MGI PMID:24736975 1322421 Gcm2 glial cells missing homolog 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10910362 1322421 Gcm2 glial cells missing homolog 2 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21765423 1322421 Gcm2 glial cells missing homolog 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21765423 1322421 Gcm2 glial cells missing homolog 2 gene MP:0013573 abnormal parathyroid gland development IAGP N RGD:5509061 20150305 MGI PMID:17382312 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:23727454 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:19251658 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:23727454 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17998389 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23663453 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19092943 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:19092943 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:19092943 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:19092943 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:20538915 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:12717433 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:19092943 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:19092943 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12717433 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17998389 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19092943 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12717433 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12717433 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:12717433 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0002574 increased vertical activity IEA N RGD:5509061 20221215 MGI 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:19251658 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:23727454 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:19092943 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:23663453 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20181227 MGI 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210128 MGI 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:17998389 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0004831 long incisors IAGP N RGD:5509061 20141003 MGI PMID:23727454 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:17998389 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17998389 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17998389 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17998389 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12717433 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:23663453 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12717433 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17998389 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23663453 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:19251658 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:23727454 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:23663453 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0006402 small molars IAGP N RGD:5509061 20141003 MGI PMID:19251658 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12717433 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:17998389 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20538915 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:19092943 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17998389 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23663453 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12717433 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17998389 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23663453 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:17998389 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17998389 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17998389 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17998389 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0008758 abnormal T cell receptor beta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:12717433 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0009263 abnormal eyelid fusion IEA N RGD:5509061 20210520 MGI 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12717433 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:12717433 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:23727454 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:23727454 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0010864 abnormal enamel knot morphology IAGP N RGD:5509061 20180118 MGI PMID:19251658 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23727454 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12717433 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19092943 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23727454 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23663453 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0013741 absent thymus corticomedullary boundary IAGP N RGD:5509061 20150430 MGI PMID:12717433 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0030079 small incisors IAGP N RGD:5509061 20170928 MGI PMID:19251658 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0030420 short basicranium IAGP N RGD:5509061 20171214 MGI PMID:23727454 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0030453 abnormal odontoblast morphology IAGP N RGD:5509061 20171221 MGI PMID:19251658 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0030471 abnormal ameloblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:19251658 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0030518 abnormal outer dental epithelium morphology IAGP N RGD:5509061 20180118 MGI PMID:19251658 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0030522 abnormal stellate reticulum morphology IAGP N RGD:5509061 20180118 MGI PMID:19251658 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0030526 abnormal enamel cord morphology IAGP N RGD:5509061 20180118 MGI PMID:19251658 1322423 Bcl11b B cell leukemia/lymphoma 11B gene MP:0030605 abnormal corneocyte morphology IAGP N RGD:5509061 20180628 MGI PMID:19092943 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20231207 MGI 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180830 MGI PMID:18922680 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:17322897 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20150430 MGI PMID:22457199 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0000578 ulcerated autopod IAGP N RGD:5509061 20240822 MGI PMID:37796769 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:17322897 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:17322897 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:17322897 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001208 blistering IAGP N RGD:5509061 20150430 MGI PMID:22457199 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001208 blistering IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001208 blistering IAGP N RGD:5509061 20180830 MGI PMID:18922680 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001208 blistering IAGP N RGD:5509061 20240822 MGI PMID:37796769 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20240822 MGI PMID:37796769 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:17322897 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20180830 MGI PMID:18922680 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17322897 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150430 MGI PMID:22457199 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20240829 MGI PMID:37796769 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001412 excessive scratching IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17322897 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20150430 MGI PMID:22457199 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001849 ear inflammation IAGP N RGD:5509061 20240822 MGI PMID:37796769 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17322897 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20240822 MGI PMID:37796769 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20150430 MGI PMID:22457199 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0002083 premature death IAGP N RGD:5509061 20240829 MGI PMID:37796769 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:17322897 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0002606 increased basophil cell number IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20240822 MGI PMID:37796769 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:17322897 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0005275 abnormal skin tensile strength IAGP N RGD:5509061 20240822 MGI PMID:37796769 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20150430 MGI PMID:22457199 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20150430 MGI PMID:22457199 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20231207 MGI 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20150430 MGI PMID:22457199 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20180830 MGI PMID:18922680 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20210128 MGI 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0009827 skin detachment IAGP N RGD:5509061 20240822 MGI PMID:37796769 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0010072 increased pruritus IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17322897 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20150430 MGI PMID:22457199 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0011159 abnormal epidermal-dermal junction morphology IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20141003 MGI PMID:17322897 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20240822 MGI PMID:37796769 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20150430 MGI PMID:22457199 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20160929 MGI PMID:25310407 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0011871 podocyte hypertrophy IAGP N RGD:5509061 20150430 MGI PMID:22457199 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0012400 nail dystrophy IAGP N RGD:5509061 20240822 MGI PMID:37796769 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0012402 abnormal nail bed morphology IAGP N RGD:5509061 20240822 MGI PMID:37796769 1322426 Col17a1 collagen, type XVII, alpha 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1322428 Cdc42ep1 CDC42 effector protein 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20221201 MGI PMID:24451259 1322428 Cdc42ep1 CDC42 effector protein 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20221201 MGI PMID:24451259 1322428 Cdc42ep1 CDC42 effector protein 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20221201 MGI PMID:24451259 1322428 Cdc42ep1 CDC42 effector protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20221201 MGI PMID:24451259 1322428 Cdc42ep1 CDC42 effector protein 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20221201 MGI PMID:24451259 1322428 Cdc42ep1 CDC42 effector protein 1 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20221201 MGI PMID:24451259 1322428 Cdc42ep1 CDC42 effector protein 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20221201 MGI PMID:24451259 1322428 Cdc42ep1 CDC42 effector protein 1 gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20221201 MGI PMID:24451259 1322428 Cdc42ep1 CDC42 effector protein 1 gene MP:0020329 decreased capillary density IAGP N RGD:5509061 20221201 MGI PMID:24451259 1322429 Exoc3l exocyst complex component 3-like gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1322429 Exoc3l exocyst complex component 3-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240328 MGI PMID:37661429 1322429 Exoc3l exocyst complex component 3-like gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220519 MGI 1322431 Ipo11 importin 11 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1322431 Ipo11 importin 11 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191205 MGI 1322431 Ipo11 importin 11 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191205 MGI 1322431 Ipo11 importin 11 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191205 MGI 1322431 Ipo11 importin 11 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1322431 Ipo11 importin 11 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191205 MGI 1322431 Ipo11 importin 11 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220519 MGI 1322431 Ipo11 importin 11 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1322431 Ipo11 importin 11 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191205 MGI 1322431 Ipo11 importin 11 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1322431 Ipo11 importin 11 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322431 Ipo11 importin 11 gene MP:0012724 absent head fold IEA N RGD:5509061 20191205 MGI 1322431 Ipo11 importin 11 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1322431 Ipo11 importin 11 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1322433 Neb nebulin gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16902413 1322433 Neb nebulin gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:23715096 1322433 Neb nebulin gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:16902413 1322433 Neb nebulin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16769824 1322433 Neb nebulin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170427 MGI PMID:26123491 1322433 Neb nebulin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200430 MGI PMID:32066503 1322433 Neb nebulin gene MP:0001265 decreased body size IAGP N RGD:5509061 20200430 MGI PMID:32066503 1322433 Neb nebulin gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:16902413 1322433 Neb nebulin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200430 MGI PMID:32066503 1322433 Neb nebulin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16902413 1322433 Neb nebulin gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:16769824 1322433 Neb nebulin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16902413 1322433 Neb nebulin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23715096 1322433 Neb nebulin gene MP:0002083 premature death IAGP N RGD:5509061 20170427 MGI PMID:26123491 1322433 Neb nebulin gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:23715096 1322433 Neb nebulin gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20200430 MGI PMID:32066503 1322433 Neb nebulin gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20170427 MGI PMID:26123491 1322433 Neb nebulin gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20200430 MGI PMID:32066503 1322433 Neb nebulin gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23715096 1322433 Neb nebulin gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16769824 1322433 Neb nebulin gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20170427 MGI PMID:26123491 1322433 Neb nebulin gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20200430 MGI PMID:32066503 1322433 Neb nebulin gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:16769824 1322433 Neb nebulin gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:16902413 1322433 Neb nebulin gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:23715096 1322433 Neb nebulin gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20170427 MGI PMID:26123491 1322433 Neb nebulin gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:16769824 1322433 Neb nebulin gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:23715096 1322433 Neb nebulin gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20170427 MGI PMID:26123491 1322433 Neb nebulin gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20170314 MGI PMID:24046450 1322433 Neb nebulin gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20170314 MGI PMID:24046450 1322433 Neb nebulin gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16902413 1322433 Neb nebulin gene MP:0009398 abnormal skeletal muscle fiber size IAGP N RGD:5509061 20170427 MGI PMID:26123491 1322433 Neb nebulin gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:23715096 1322433 Neb nebulin gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20200430 MGI PMID:32066503 1322433 Neb nebulin gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20200430 MGI PMID:32066503 1322433 Neb nebulin gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20200430 MGI PMID:32066503 1322433 Neb nebulin gene MP:0009405 increased skeletal muscle fiber number IAGP N RGD:5509061 20170427 MGI PMID:26123491 1322433 Neb nebulin gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20170427 MGI PMID:26123491 1322433 Neb nebulin gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20200430 MGI PMID:32066503 1322433 Neb nebulin gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16769824 1322433 Neb nebulin gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200430 MGI PMID:32066503 1322433 Neb nebulin gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20170427 MGI PMID:26123491 1322433 Neb nebulin gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20170427 MGI PMID:26123491 1322433 Neb nebulin gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16902413 1322433 Neb nebulin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16769824 1322433 Neb nebulin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23715096 1322433 Neb nebulin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16902413 1322433 Neb nebulin gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200430 MGI PMID:32066503 1322433 Neb nebulin gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20170427 MGI PMID:26123491 1322433 Neb nebulin gene MP:0030566 abnormal A band morphology IAGP N RGD:5509061 20180531 MGI PMID:16769824 1322433 Neb nebulin gene MP:0030566 abnormal A band morphology IAGP N RGD:5509061 20180531 MGI PMID:26123491 1322433 Neb nebulin gene MP:0030567 abnormal I band morphology IAGP N RGD:5509061 20180531 MGI PMID:16769824 1322433 Neb nebulin gene MP:0030568 abnormal H zone morphology IAGP N RGD:5509061 20180531 MGI PMID:16902413 1322433 Neb nebulin gene MP:0030568 abnormal H zone morphology IAGP N RGD:5509061 20180531 MGI PMID:26123491 1322434 Aasdh aminoadipate-semialdehyde dehydrogenase gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1322434 Aasdh aminoadipate-semialdehyde dehydrogenase gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220519 MGI 1322434 Aasdh aminoadipate-semialdehyde dehydrogenase gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20221215 MGI 1322436 Tmem259 transmembrane protein 259 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1322441 Aire autoimmune regulator gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16709926 1322441 Aire autoimmune regulator gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16709926 1322441 Aire autoimmune regulator gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:19015306 1322441 Aire autoimmune regulator gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:22490868 1322441 Aire autoimmune regulator gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:22490868 1322441 Aire autoimmune regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16709926 1322441 Aire autoimmune regulator gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:16172259 1322441 Aire autoimmune regulator gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:20696775 1322441 Aire autoimmune regulator gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1322441 Aire autoimmune regulator gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:16172259 1322441 Aire autoimmune regulator gene MP:0001337 dry eyes IAGP N RGD:5509061 20141003 MGI PMID:20696775 1322441 Aire autoimmune regulator gene MP:0001346 abnormal lacrimal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:20696775 1322441 Aire autoimmune regulator gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22490868 1322441 Aire autoimmune regulator gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16709926 1322441 Aire autoimmune regulator gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:19265170 1322441 Aire autoimmune regulator gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:15699112 1322441 Aire autoimmune regulator gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:19015306 1322441 Aire autoimmune regulator gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22490868 1322441 Aire autoimmune regulator gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11854172 1322441 Aire autoimmune regulator gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:16172259 1322441 Aire autoimmune regulator gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:16709926 1322441 Aire autoimmune regulator gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:16172259 1322441 Aire autoimmune regulator gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0001868 ovary inflammation IAGP N RGD:5509061 20141003 MGI PMID:16172259 1322441 Aire autoimmune regulator gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:16172259 1322441 Aire autoimmune regulator gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141211 MGI PMID:15699112 1322441 Aire autoimmune regulator gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:16172259 1322441 Aire autoimmune regulator gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20230622 MGI PMID:15699112 1322441 Aire autoimmune regulator gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:15699112 1322441 Aire autoimmune regulator gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:16172259 1322441 Aire autoimmune regulator gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:17360567 1322441 Aire autoimmune regulator gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:21182094 1322441 Aire autoimmune regulator gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:11854172 1322441 Aire autoimmune regulator gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15699112 1322441 Aire autoimmune regulator gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:19265170 1322441 Aire autoimmune regulator gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:11854172 1322441 Aire autoimmune regulator gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16709926 1322441 Aire autoimmune regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16172259 1322441 Aire autoimmune regulator gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20170105 MGI 1322441 Aire autoimmune regulator gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16709926 1322441 Aire autoimmune regulator gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20404099 1322441 Aire autoimmune regulator gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16709926 1322441 Aire autoimmune regulator gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:12376594 1322441 Aire autoimmune regulator gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:19265170 1322441 Aire autoimmune regulator gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:21182094 1322441 Aire autoimmune regulator gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:22490868 1322441 Aire autoimmune regulator gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:16172259 1322441 Aire autoimmune regulator gene MP:0003341 chronic pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0003504 thyroid gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:16172259 1322441 Aire autoimmune regulator gene MP:0003504 thyroid gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0003608 prostate gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:16172259 1322441 Aire autoimmune regulator gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:22490868 1322441 Aire autoimmune regulator gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:11854172 1322441 Aire autoimmune regulator gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:11854172 1322441 Aire autoimmune regulator gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:15699112 1322441 Aire autoimmune regulator gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:16172259 1322441 Aire autoimmune regulator gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:17360567 1322441 Aire autoimmune regulator gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:19265170 1322441 Aire autoimmune regulator gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:22490868 1322441 Aire autoimmune regulator gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:19015306 1322441 Aire autoimmune regulator gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:22490868 1322441 Aire autoimmune regulator gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21182094 1322441 Aire autoimmune regulator gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16709926 1322441 Aire autoimmune regulator gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21300913 1322441 Aire autoimmune regulator gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16709926 1322441 Aire autoimmune regulator gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12376594 1322441 Aire autoimmune regulator gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:16172259 1322441 Aire autoimmune regulator gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20201022 MGI 1322441 Aire autoimmune regulator gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20141003 MGI PMID:11854172 1322441 Aire autoimmune regulator gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11854172 1322441 Aire autoimmune regulator gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:12376594 1322441 Aire autoimmune regulator gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:21182094 1322441 Aire autoimmune regulator gene MP:0005398 decreased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:21182094 1322441 Aire autoimmune regulator gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:21182094 1322441 Aire autoimmune regulator gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22490868 1322441 Aire autoimmune regulator gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:21182094 1322441 Aire autoimmune regulator gene MP:0005515 uveitis IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0005515 uveitis IAGP N RGD:5509061 20141003 MGI PMID:19265170 1322441 Aire autoimmune regulator gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20696775 1322441 Aire autoimmune regulator gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0006194 keratoconjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:20696775 1322441 Aire autoimmune regulator gene MP:0006201 vitreous body inflammation IAGP N RGD:5509061 20141003 MGI PMID:19265170 1322441 Aire autoimmune regulator gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11854172 1322441 Aire autoimmune regulator gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:21300913 1322441 Aire autoimmune regulator gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:21300913 1322441 Aire autoimmune regulator gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:16709926 1322441 Aire autoimmune regulator gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16709926 1322441 Aire autoimmune regulator gene MP:0008241 abnormal metallophilic macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:16709926 1322441 Aire autoimmune regulator gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21182094 1322441 Aire autoimmune regulator gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:21182094 1322441 Aire autoimmune regulator gene MP:0008690 increased interleukin-23 secretion IAGP N RGD:5509061 20141003 MGI PMID:21182094 1322441 Aire autoimmune regulator gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21182094 1322441 Aire autoimmune regulator gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:21182094 1322441 Aire autoimmune regulator gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:22490868 1322441 Aire autoimmune regulator gene MP:0008879 submandibular gland inflammation IAGP N RGD:5509061 20141211 MGI PMID:15699112 1322441 Aire autoimmune regulator gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:18414681 1322441 Aire autoimmune regulator gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:20696775 1322441 Aire autoimmune regulator gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141204 MGI PMID:15699112 1322441 Aire autoimmune regulator gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20201022 MGI 1322441 Aire autoimmune regulator gene MP:0009540 absent Hassall's corpuscle IAGP N RGD:5509061 20141003 MGI PMID:19015306 1322441 Aire autoimmune regulator gene MP:0010222 abnormal T-helper 17 cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21182094 1322441 Aire autoimmune regulator gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:15699112 1322441 Aire autoimmune regulator gene MP:0012164 abnormal conjunctiva goblet cell morphology IAGP N RGD:5509061 20141204 MGI PMID:20696775 1322441 Aire autoimmune regulator gene MP:0013367 parotid gland inflammation IAGP N RGD:5509061 20141218 MGI PMID:15699112 1322441 Aire autoimmune regulator gene MP:0013367 parotid gland inflammation IAGP N RGD:5509061 20141218 MGI PMID:19265170 1322441 Aire autoimmune regulator gene MP:0013533 sublingual gland inflammation IAGP N RGD:5509061 20150219 MGI PMID:19265170 1322441 Aire autoimmune regulator gene MP:0013754 abnormal ocular surface morphology IAGP N RGD:5509061 20150416 MGI PMID:20696775 1322441 Aire autoimmune regulator gene MP:0020220 decreased tear production IAGP N RGD:5509061 20141211 MGI PMID:15699112 1322441 Aire autoimmune regulator gene MP:0031226 increased CXCL10 level IAGP N RGD:5509061 20210218 MGI PMID:22490868 1322444 Angptl6 angiopoietin-like 6 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322444 Angptl6 angiopoietin-like 6 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322444 Angptl6 angiopoietin-like 6 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322444 Angptl6 angiopoietin-like 6 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322444 Angptl6 angiopoietin-like 6 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322444 Angptl6 angiopoietin-like 6 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322444 Angptl6 angiopoietin-like 6 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322444 Angptl6 angiopoietin-like 6 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322444 Angptl6 angiopoietin-like 6 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322444 Angptl6 angiopoietin-like 6 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322444 Angptl6 angiopoietin-like 6 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322444 Angptl6 angiopoietin-like 6 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322444 Angptl6 angiopoietin-like 6 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322444 Angptl6 angiopoietin-like 6 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322444 Angptl6 angiopoietin-like 6 gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322444 Angptl6 angiopoietin-like 6 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15778720 1322445 Garin5a golgi associated RAB2 interactor 5A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20240801 MGI PMID:38935810 1322445 Garin5a golgi associated RAB2 interactor 5A gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240801 MGI PMID:38935810 1322445 Garin5a golgi associated RAB2 interactor 5A gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240801 MGI PMID:38935810 1322445 Garin5a golgi associated RAB2 interactor 5A gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20240801 MGI PMID:38935810 1322447 Dsg2 desmoglein 2 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:12494996 1322447 Dsg2 desmoglein 2 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20210429 MGI PMID:30115995 1322447 Dsg2 desmoglein 2 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20190502 MGI 1322447 Dsg2 desmoglein 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20210204 MGI PMID:27170944 1322447 Dsg2 desmoglein 2 gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20210128 MGI 1322447 Dsg2 desmoglein 2 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20210204 MGI PMID:27170944 1322447 Dsg2 desmoglein 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20210204 MGI PMID:27170944 1322447 Dsg2 desmoglein 2 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20210204 MGI PMID:27170944 1322447 Dsg2 desmoglein 2 gene MP:0003898 abnormal QRS complex IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20210204 MGI PMID:27170944 1322447 Dsg2 desmoglein 2 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20210204 MGI PMID:27170944 1322447 Dsg2 desmoglein 2 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20210429 MGI PMID:30115995 1322447 Dsg2 desmoglein 2 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20210204 MGI PMID:27170944 1322447 Dsg2 desmoglein 2 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210204 MGI PMID:27170944 1322447 Dsg2 desmoglein 2 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20210204 MGI PMID:27170944 1322447 Dsg2 desmoglein 2 gene MP:0010394 decreased QRS amplitude IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20210204 MGI PMID:27170944 1322447 Dsg2 desmoglein 2 gene MP:0010509 decreased P wave amplitude IAGP N RGD:5509061 20210204 MGI PMID:27170944 1322447 Dsg2 desmoglein 2 gene MP:0010631 increased Q wave amplitude IAGP N RGD:5509061 20210204 MGI PMID:27170944 1322447 Dsg2 desmoglein 2 gene MP:0010759 decreased right ventricle systolic pressure IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12494996 1322447 Dsg2 desmoglein 2 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12494996 1322447 Dsg2 desmoglein 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1322447 Dsg2 desmoglein 2 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:12494996 1322447 Dsg2 desmoglein 2 gene MP:0011920 abnormal S wave IAGP N RGD:5509061 20210204 MGI PMID:27170944 1322447 Dsg2 desmoglein 2 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20210204 MGI PMID:27170944 1322447 Dsg2 desmoglein 2 gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20210429 MGI PMID:30115995 1322447 Dsg2 desmoglein 2 gene MP:0030578 decreased keratinocyte adhesion IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0031533 abnormal heart left ventricle wall morphology IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322447 Dsg2 desmoglein 2 gene MP:0031534 abnormal heart right ventricle wall morphology IAGP N RGD:5509061 20240118 MGI PMID:36268721 1322451 Mdp1 magnesium-dependent phosphatase 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20170105 MGI 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20160421 MGI 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210826 MGI 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0001505 hunched posture IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0001511 disheveled coat IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0002083 premature death IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20160421 MGI 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0002861 abnormal tail bud morphology IEA N RGD:5509061 20201022 MGI 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0002871 albuminuria IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0002989 small kidney IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20220519 MGI 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0004969 pale kidney IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20170105 MGI 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0008062 abnormal podocyte slit junction morphology IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0011402 renal cast IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0013139 moribund IAGP N RGD:5509061 20201015 MGI PMID:30737270 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1322455 Coq6 coenzyme Q6 monooxygenase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1322458 Ccnt1 cyclin T1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1322458 Ccnt1 cyclin T1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1322458 Ccnt1 cyclin T1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1322458 Ccnt1 cyclin T1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220811 MGI 1322458 Ccnt1 cyclin T1 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20230622 MGI PMID:17938200 1322458 Ccnt1 cyclin T1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20230622 MGI PMID:17938200 1322458 Ccnt1 cyclin T1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1322458 Ccnt1 cyclin T1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1322458 Ccnt1 cyclin T1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1322458 Ccnt1 cyclin T1 gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20230622 MGI PMID:17938200 1322458 Ccnt1 cyclin T1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1322458 Ccnt1 cyclin T1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1322458 Ccnt1 cyclin T1 gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20230622 MGI PMID:17938200 1322462 Il33 interleukin 33 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20230601 MGI 1322462 Il33 interleukin 33 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20190418 MGI PMID:28675392 1322462 Il33 interleukin 33 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20160922 MGI PMID:25617473 1322462 Il33 interleukin 33 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20160922 MGI PMID:25617473 1322462 Il33 interleukin 33 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20160922 MGI PMID:25617473 1322462 Il33 interleukin 33 gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23248269 1322462 Il33 interleukin 33 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:20937871 1322462 Il33 interleukin 33 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:20937871 1322462 Il33 interleukin 33 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20211202 MGI PMID:32240120 1322462 Il33 interleukin 33 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20190418 MGI PMID:28675392 1322462 Il33 interleukin 33 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:20937871 1322462 Il33 interleukin 33 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:22331917 1322462 Il33 interleukin 33 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20190418 MGI PMID:28675392 1322462 Il33 interleukin 33 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20160922 MGI PMID:25617473 1322462 Il33 interleukin 33 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20190418 MGI PMID:28675392 1322462 Il33 interleukin 33 gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20160922 MGI PMID:25617473 1322462 Il33 interleukin 33 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20160922 MGI PMID:25617473 1322462 Il33 interleukin 33 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20190418 MGI PMID:28675392 1322462 Il33 interleukin 33 gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20190418 MGI PMID:28675392 1322462 Il33 interleukin 33 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22331917 1322462 Il33 interleukin 33 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23248269 1322462 Il33 interleukin 33 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:22331917 1322462 Il33 interleukin 33 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:23248269 1322462 Il33 interleukin 33 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1322462 Il33 interleukin 33 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:22331917 1322462 Il33 interleukin 33 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20160922 MGI PMID:25617473 1322462 Il33 interleukin 33 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20190418 MGI PMID:28675392 1322462 Il33 interleukin 33 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20937871 1322462 Il33 interleukin 33 gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:20937871 1322462 Il33 interleukin 33 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20937871 1322462 Il33 interleukin 33 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20937871 1322462 Il33 interleukin 33 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:20937871 1322462 Il33 interleukin 33 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20160922 MGI PMID:25617473 1322462 Il33 interleukin 33 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20937871 1322462 Il33 interleukin 33 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1322462 Il33 interleukin 33 gene MP:0010862 decreased respiratory mucosa goblet cell number IAGP N RGD:5509061 20141003 MGI PMID:22331917 1322462 Il33 interleukin 33 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20190418 MGI PMID:28675392 1322462 Il33 interleukin 33 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20190418 MGI PMID:28675392 1322462 Il33 interleukin 33 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:28675392 1322462 Il33 interleukin 33 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:25617473 1322468 Brf1 BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit gene MP:0000601 small liver IAGP N RGD:5509061 20200423 MGI PMID:30858608 1322468 Brf1 BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200423 MGI PMID:30858608 1322468 Brf1 BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20200423 MGI PMID:30858608 1322468 Brf1 BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200423 MGI PMID:30858608 1322468 Brf1 BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit gene MP:0002083 premature death IAGP N RGD:5509061 20200423 MGI PMID:30858608 1322468 Brf1 BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200423 MGI PMID:30858608 1322468 Brf1 BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20200423 MGI PMID:30858608 1322468 Brf1 BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit gene MP:0003695 delayed blastocyst hatching from the zona pellucida IAGP N RGD:5509061 20200423 MGI PMID:30858608 1322468 Brf1 BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20200423 MGI PMID:30858608 1322468 Brf1 BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20200423 MGI PMID:30858608 1322468 Brf1 BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200423 MGI PMID:30858608 1322468 Brf1 BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200423 MGI PMID:30858608 1322468 Brf1 BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200423 MGI PMID:30858608 1322468 Brf1 BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit gene MP:0012129 failure of blastocyst formation IAGP N RGD:5509061 20200423 MGI PMID:30858608 1322468 Brf1 BRF1, RNA polymerase III transcription initiation factor 90 kDa subunit gene MP:0013272 abnormal translation IAGP N RGD:5509061 20200423 MGI PMID:30858608 1322470 Alox12 arachidonate 12-lipoxygenase gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:10383730 1322470 Alox12 arachidonate 12-lipoxygenase gene MP:0009586 increased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:9501222 1322470 Alox12 arachidonate 12-lipoxygenase gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:9501222 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0000754 paresis IAGP N RGD:5509061 20151224 MGI PMID:26642356 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151224 MGI PMID:26642356 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20151224 MGI PMID:26642356 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20473324 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20151224 MGI PMID:26642356 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0001924 infertility IAGP N RGD:5509061 20151224 MGI PMID:26642356 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20151224 MGI PMID:26642356 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0002959 increased urine microalbumin level IEA N RGD:5509061 20181227 MGI 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0003708 binucleate IAGP N RGD:5509061 20141003 MGI PMID:20473324 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:20473324 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:20473324 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20473324 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20151224 MGI PMID:26642356 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20151224 MGI PMID:26642356 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20151224 MGI PMID:26642356 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:20473324 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:20473324 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20473324 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20473324 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20473324 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20473324 1322472 Nek7 NIMA (never in mitosis gene a)-related expressed kinase 7 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20473324 1322473 Ufsp2 UFM1-specific peptidase 2 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1322473 Ufsp2 UFM1-specific peptidase 2 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1322473 Ufsp2 UFM1-specific peptidase 2 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1322473 Ufsp2 UFM1-specific peptidase 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1322473 Ufsp2 UFM1-specific peptidase 2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1322473 Ufsp2 UFM1-specific peptidase 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1322473 Ufsp2 UFM1-specific peptidase 2 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1322473 Ufsp2 UFM1-specific peptidase 2 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1322473 Ufsp2 UFM1-specific peptidase 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1322473 Ufsp2 UFM1-specific peptidase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322473 Ufsp2 UFM1-specific peptidase 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1322473 Ufsp2 UFM1-specific peptidase 2 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1322475 Fam20b FAM20B, glycosaminoglycan xylosylkinase gene MP:0000597 delayed hepatic development IAGP N RGD:5509061 20141003 MGI PMID:22732358 1322475 Fam20b FAM20B, glycosaminoglycan xylosylkinase gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:22732358 1322475 Fam20b FAM20B, glycosaminoglycan xylosylkinase gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:22732358 1322475 Fam20b FAM20B, glycosaminoglycan xylosylkinase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22732358 1322475 Fam20b FAM20B, glycosaminoglycan xylosylkinase gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:22732358 1322475 Fam20b FAM20B, glycosaminoglycan xylosylkinase gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 1322475 Fam20b FAM20B, glycosaminoglycan xylosylkinase gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 1322475 Fam20b FAM20B, glycosaminoglycan xylosylkinase gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:22732358 1322475 Fam20b FAM20B, glycosaminoglycan xylosylkinase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22732358 1322477 Cdc14b CDC14 cell division cycle 14B gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:21262768 1322477 Cdc14b CDC14 cell division cycle 14B gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:21262768 1322477 Cdc14b CDC14 cell division cycle 14B gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:21262768 1322477 Cdc14b CDC14 cell division cycle 14B gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:21262768 1322477 Cdc14b CDC14 cell division cycle 14B gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:21262768 1322477 Cdc14b CDC14 cell division cycle 14B gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:21262768 1322477 Cdc14b CDC14 cell division cycle 14B gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:21262768 1322477 Cdc14b CDC14 cell division cycle 14B gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:21262768 1322477 Cdc14b CDC14 cell division cycle 14B gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21262768 1322477 Cdc14b CDC14 cell division cycle 14B gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:21262768 1322477 Cdc14b CDC14 cell division cycle 14B gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21262768 1322477 Cdc14b CDC14 cell division cycle 14B gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:21262768 1322477 Cdc14b CDC14 cell division cycle 14B gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21262768 1322477 Cdc14b CDC14 cell division cycle 14B gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20230810 MGI PMID:21262768 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200402 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20210128 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210128 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20200402 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0011939 increased food intake IEA N RGD:5509061 20211021 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0013426 decreased memory-marker NK cell number IEA N RGD:5509061 20201231 MGI 1322479 D6Wsu163e DNA segment, Chr 6, Wayne State University 163, expressed gene MP:0013436 increased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0000161 scoliosis IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0000445 short snout IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0000629 absent mammary gland IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322481 Dhx35 DEAH-box helicase 35 gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0003451 absent olfactory bulb IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0004158 right aortic arch IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0004163 abnormal adenohypophysis morphology IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0004463 basisphenoid bone foramen IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322481 Dhx35 DEAH-box helicase 35 gene MP:0005157 holoprosencephaly IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0008128 abnormal brain internal capsule morphology IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0008923 thoracoschisis IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0010589 common truncal valve IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322481 Dhx35 DEAH-box helicase 35 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0013186 abnormal basilar artery morphology IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0013952 retroesophageal left subclavian artery IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0013970 absent connection between subcutaneous lymph vessels and lymph sac IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0013977 symmetric azygos veins IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0013981 double lumen aortic arch IEA N RGD:5509061 20170504 MGI 1322481 Dhx35 DEAH-box helicase 35 gene MP:0013996 abnormal vertebral artery origin IEA N RGD:5509061 20170504 MGI 1322485 Gemin6 gem nuclear organelle associated protein 6 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1322485 Gemin6 gem nuclear organelle associated protein 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1322489 Pate4 prostate and testis expressed 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1322489 Pate4 prostate and testis expressed 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20190926 MGI PMID:30452524 1322489 Pate4 prostate and testis expressed 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20190926 MGI PMID:30452524 1322489 Pate4 prostate and testis expressed 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20161117 MGI PMID:26731031 1322489 Pate4 prostate and testis expressed 4 gene MP:0002673 abnormal sperm number IAGP N RGD:5509061 20190926 MGI PMID:30452524 1322489 Pate4 prostate and testis expressed 4 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1322489 Pate4 prostate and testis expressed 4 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1322489 Pate4 prostate and testis expressed 4 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1322489 Pate4 prostate and testis expressed 4 gene MP:0030982 abnormal copulatory plug deposition IAGP N RGD:5509061 20191017 MGI PMID:30452524 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:10932191 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:14651926 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141120 MGI PMID:23413832 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000508 right-sided isomerism IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:14651926 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000650 mesocardia IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000690 absent spleen IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20190808 MGI PMID:22355535 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20190808 MGI PMID:22355535 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20190808 MGI PMID:22355535 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141120 MGI PMID:23413832 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000923 abnormal roof plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:14651926 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141120 MGI PMID:23413832 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141120 MGI PMID:23413832 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20190808 MGI PMID:22355535 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190808 MGI PMID:22355535 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20190808 MGI PMID:22355535 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:11699604 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0002224 abnormal spleen size IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:10932191 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:14651926 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:23555929 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:14651926 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141120 MGI PMID:23413832 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20190808 MGI PMID:22355535 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0003895 increased ectoderm apoptosis IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0004387 abnormal prechordal plate morphology IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0004639 fused metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0004642 fused metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0005163 cyclopia IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0005163 cyclopia IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20190808 MGI PMID:22355535 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0006290 proboscis IAGP N RGD:5509061 20170314 MGI PMID:18617531 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141120 MGI PMID:23413832 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20190808 MGI PMID:22355535 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20190808 MGI PMID:22355535 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20190808 MGI PMID:22355535 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0008817 hematoma IAGP N RGD:5509061 20141003 MGI PMID:14651926 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0008919 fused tarsal bones IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20190808 MGI PMID:22355535 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:11699604 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20170314 MGI PMID:27466203 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20190808 MGI PMID:22355535 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20190808 MGI PMID:22355535 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0009843 decreased neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:14651926 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141120 MGI PMID:23413832 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141120 MGI PMID:23413832 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14651926 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20170314 MGI PMID:27466203 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0012709 delayed caudal neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:14651926 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0012793 decreased rhombomere 3 size IAGP N RGD:5509061 20141003 MGI PMID:14651926 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0012801 decreased rhombomere 5 size IAGP N RGD:5509061 20141003 MGI PMID:14651926 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0013001 abnormal enteric neural crest cell morphology IAGP N RGD:5509061 20141120 MGI PMID:23413832 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0013973 abnormal hepatic vein connection IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0014277 alobar holoprosencephaly IAGP N RGD:5509061 20230810 MGI PMID:29992973 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0014320 abnormal autopod rotation IAGP N RGD:5509061 20240404 MGI PMID:10677508 1322492 Zic2 zinc finger protein of the cerebellum 2 gene MP:0020494 left sided inferior vena cava IAGP N RGD:5509061 20191128 MGI PMID:29992973 1322499 Tbata thymus, brain and testes associated gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20937703 1322499 Tbata thymus, brain and testes associated gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:20937703 1322499 Tbata thymus, brain and testes associated gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20937703 1322499 Tbata thymus, brain and testes associated gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20937703 1322499 Tbata thymus, brain and testes associated gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20937703 1322499 Tbata thymus, brain and testes associated gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:20937703 1322499 Tbata thymus, brain and testes associated gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20937703 1322499 Tbata thymus, brain and testes associated gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20937703 1322501 Gdf7 growth differentiation factor 7 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15975937 1322501 Gdf7 growth differentiation factor 7 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23364326 1322501 Gdf7 growth differentiation factor 7 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9808626 1322501 Gdf7 growth differentiation factor 7 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:15975937 1322501 Gdf7 growth differentiation factor 7 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:23364326 1322501 Gdf7 growth differentiation factor 7 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:9808626 1322501 Gdf7 growth differentiation factor 7 gene MP:0000829 dilated fourth ventricle IAGP N RGD:5509061 20141003 MGI PMID:9808626 1322501 Gdf7 growth differentiation factor 7 gene MP:0000924 absent roof plate IAGP N RGD:5509061 20141003 MGI PMID:10693795 1322501 Gdf7 growth differentiation factor 7 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10693795 1322501 Gdf7 growth differentiation factor 7 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:15975937 1322501 Gdf7 growth differentiation factor 7 gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:11356025 1322501 Gdf7 growth differentiation factor 7 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:11356025 1322501 Gdf7 growth differentiation factor 7 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:9808626 1322501 Gdf7 growth differentiation factor 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11356025 1322501 Gdf7 growth differentiation factor 7 gene MP:0002059 abnormal seminal vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11356025 1322501 Gdf7 growth differentiation factor 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11356025 1322501 Gdf7 growth differentiation factor 7 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10693795 1322501 Gdf7 growth differentiation factor 7 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:23364326 1322501 Gdf7 growth differentiation factor 7 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:15975937 1322501 Gdf7 growth differentiation factor 7 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:10693795 1322501 Gdf7 growth differentiation factor 7 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:10693795 1322501 Gdf7 growth differentiation factor 7 gene MP:0013318 abnormal branching involved in seminal vesicle morphogenesis IAGP N RGD:5509061 20141204 MGI PMID:11356025 1322501 Gdf7 growth differentiation factor 7 gene MP:0013899 abnormal seminal vesicle epithelium morphology IAGP N RGD:5509061 20150924 MGI PMID:11356025 1322501 Gdf7 growth differentiation factor 7 gene MP:0021091 abnormal dorsal interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:10693795 1322501 Gdf7 growth differentiation factor 7 gene MP:0021092 abnormal dorsal interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:9808626 1322507 Sephs1 selenophosphate synthetase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180809 MGI PMID:27208177 1322507 Sephs1 selenophosphate synthetase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180809 MGI PMID:27208177 1322507 Sephs1 selenophosphate synthetase 1 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20180809 MGI PMID:27208177 1322507 Sephs1 selenophosphate synthetase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180809 MGI PMID:27208177 1322507 Sephs1 selenophosphate synthetase 1 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20180809 MGI PMID:27208177 1322507 Sephs1 selenophosphate synthetase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180809 MGI PMID:27208177 1322507 Sephs1 selenophosphate synthetase 1 gene MP:0030599 decreased liver manganese level IAGP N RGD:5509061 20180809 MGI PMID:27208177 1322508 Vps13b vacuolar protein sorting 13B gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20221215 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0000692 small spleen IEA N RGD:5509061 20220519 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0001147 small testis IAGP N RGD:5509061 20201105 MGI PMID:31218450 1322508 Vps13b vacuolar protein sorting 13B gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201022 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0001304 cataract IAGP N RGD:5509061 20201105 MGI PMID:32915983 1322508 Vps13b vacuolar protein sorting 13B gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20201105 MGI PMID:32915983 1322508 Vps13b vacuolar protein sorting 13B gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20210513 MGI PMID:31495077 1322508 Vps13b vacuolar protein sorting 13B gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210513 MGI PMID:31495077 1322508 Vps13b vacuolar protein sorting 13B gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0001488 increased startle reflex IEA N RGD:5509061 20200514 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0001851 eye inflammation IAGP N RGD:5509061 20201105 MGI PMID:32915983 1322508 Vps13b vacuolar protein sorting 13B gene MP:0001925 male infertility IAGP N RGD:5509061 20201105 MGI PMID:31218450 1322508 Vps13b vacuolar protein sorting 13B gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0002188 small heart IEA N RGD:5509061 20220519 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0002686 globozoospermia IAGP N RGD:5509061 20201105 MGI PMID:31218450 1322508 Vps13b vacuolar protein sorting 13B gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20201105 MGI PMID:31218450 1322508 Vps13b vacuolar protein sorting 13B gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20201105 MGI PMID:32915983 1322508 Vps13b vacuolar protein sorting 13B gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0003381 vitreal fibroplasia IAGP N RGD:5509061 20220331 MGI PMID:32915983 1322508 Vps13b vacuolar protein sorting 13B gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20200514 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20221215 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20201105 MGI PMID:31218450 1322508 Vps13b vacuolar protein sorting 13B gene MP:0008839 absent acrosome IAGP N RGD:5509061 20201105 MGI PMID:31218450 1322508 Vps13b vacuolar protein sorting 13B gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20201105 MGI PMID:31218450 1322508 Vps13b vacuolar protein sorting 13B gene MP:0009325 necrospermia IAGP N RGD:5509061 20201105 MGI PMID:31218450 1322508 Vps13b vacuolar protein sorting 13B gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1322508 Vps13b vacuolar protein sorting 13B gene MP:0010255 cortical cataract IAGP N RGD:5509061 20201105 MGI PMID:32915983 1322508 Vps13b vacuolar protein sorting 13B gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20201105 MGI PMID:31218450 1322508 Vps13b vacuolar protein sorting 13B gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20210513 MGI PMID:31495077 1322508 Vps13b vacuolar protein sorting 13B gene MP:0013732 mature cataract IAGP N RGD:5509061 20201105 MGI PMID:32915983 1322508 Vps13b vacuolar protein sorting 13B gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20201105 MGI PMID:31218450 1322508 Vps13b vacuolar protein sorting 13B gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20201105 MGI PMID:31218450 1322508 Vps13b vacuolar protein sorting 13B gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20201105 MGI PMID:31218450 1322508 Vps13b vacuolar protein sorting 13B gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:32915983 1322508 Vps13b vacuolar protein sorting 13B gene MP:0030949 abnormal Golgi vesicle transport IAGP N RGD:5509061 20201105 MGI PMID:31218450 1322508 Vps13b vacuolar protein sorting 13B gene MP:0030952 abnormal Golgi stack morphology IAGP N RGD:5509061 20201105 MGI PMID:31218450 1322508 Vps13b vacuolar protein sorting 13B gene MP:0030980 abnormal acroplaxome morphology IAGP N RGD:5509061 20201105 MGI PMID:31218450 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0000079 abnormal basioccipital bone morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0000141 abnormal vertebral body morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0000297 abnormal atrioventricular cushion morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0000445 short snout IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0000600 liver hypoplasia IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0000632 abnormal pineal gland morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0000963 fused dorsal root ganglion IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0001879 abnormal lymphatic vessel morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0002083 premature death IAGP N RGD:5509061 20160310 MGI PMID:25259869 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0002108 abnormal muscle morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0002191 abnormal artery morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0002237 abnormal nasal cavity morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0002239 abnormal nasal septum morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0002243 abnormal vomeronasal organ morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0002249 abnormal larynx morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0002746 abnormal semilunar valve morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0002951 small thyroid gland IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0003253 dilated bile duct IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0003584 bifid ureter IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0003617 urinary bladder hypoplasia IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0003924 diaphragmatic hernia IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0004110 transposition of great arteries IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0004163 abnormal adenohypophysis morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0004201 fetal growth retardation IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0004463 basisphenoid bone foramen IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0004666 absent stapedial artery IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20160310 MGI PMID:25259869 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0005269 abnormal occipital bone morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0006065 abnormal heart position or orientation IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0008386 absent styloid process IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0008534 enlarged fourth ventricle IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0008536 enlarged third ventricle IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0008922 abnormal cervical rib IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0008923 thoracoschisis IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0009526 absent sublingual gland IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20170622 MGI PMID:25259869 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0009570 abnormal right lung morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0009820 abnormal liver vasculature morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20160310 MGI PMID:25259869 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0009917 abnormal hyoid bone body morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010403 atrial septal defect IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010404 ostium primum atrial septal defect IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010433 double inlet heart left ventricle IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010439 abnormal hepatic vein morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010484 bicuspid aortic valve IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010496 abnormal pectinate muscle morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010527 bicuspid pulmonary valve IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010530 cerebral arteriovenous malformation IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010572 persistent right dorsal aorta IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010595 abnormal aortic valve cusp morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010602 abnormal pulmonary valve cusp morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010728 fusion of atlas and occipital bones IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010853 abnormal lung position or orientation IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0010912 herniated liver IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20160310 MGI PMID:25259869 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20160310 MGI PMID:25259869 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20160310 MGI PMID:25259869 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20160310 MGI PMID:25259869 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0011361 pelvic kidney IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0011493 double ureter IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013186 abnormal basilar artery morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013818 abnormal oral cavity morphology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013826 absent hypoglossal canal IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013845 abnormal eye muscle topology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013846 retropharyngeal edema IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013847 retropleural edema IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013852 abnormal Mullerian duct topology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013855 absent celiac artery IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013871 abnormal stapedial artery topology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013878 abnormal ductus venosus valve topology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013917 persistent right 6th pharyngeal arch artery IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013923 small prevertebral sympathetic ganglia IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013925 abnormal vascular plexus formation IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013930 abnormal digastric muscle connection IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013931 abnormal olfactory bulb position IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013932 fragmented Meckel's cartilage IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013936 abnormal thymus topology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013949 fusion of axis and occipital bones IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013965 abnormally deep median sulcus of tongue IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013970 absent connection between subcutaneous lymph vessels and lymph sac IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013976 abnormal left vena cava superior connection IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013977 symmetric azygos veins IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013982 inverse situs of great intrathoracic arteries IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013996 abnormal vertebral artery origin IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013998 absent canalicular internal carotid artery segment IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0013999 absent parasellar internal carotid artery IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0014011 abnormal ovary tissue architecture IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0014017 abnormal Wolffian duct connection IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0014019 embryo cyst IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0020301 short tongue IEA N RGD:5509061 20170504 MGI 1322511 Sh3pxd2a SH3 and PX domains 2A gene MP:0020500 persistent trigeminal artery IEA N RGD:5509061 20180628 MGI 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000088 short mandible IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000088 short mandible IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000088 short mandible IAGP N RGD:5509061 20210722 MGI PMID:32991838 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000097 short maxilla IAGP N RGD:5509061 20170209 MGI PMID:26234751 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20170209 MGI PMID:16203988 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20170209 MGI PMID:16203988 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20170209 MGI PMID:21484342 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20170209 MGI PMID:16203988 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000154 rib fusion IAGP N RGD:5509061 20170209 MGI PMID:23236180 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000158 absent sternum IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000160 kyphosis IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20170209 MGI PMID:16207837 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20170209 MGI PMID:23907671 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20170209 MGI PMID:19261698 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20170209 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20170209 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20170209 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20170209 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20170209 MGI PMID:24191021 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20170209 MGI PMID:16085486 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20170209 MGI PMID:16085486 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20170209 MGI PMID:16085486 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000414 alopecia IAGP N RGD:5509061 20170209 MGI PMID:16085486 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000435 shortened head IAGP N RGD:5509061 20170209 MGI PMID:26234751 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000440 domed cranium IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000440 domed cranium IAGP N RGD:5509061 20170209 MGI PMID:26234751 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000445 short snout IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000445 short snout IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000445 short snout IAGP N RGD:5509061 20170209 MGI PMID:26234751 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20210722 MGI PMID:32991838 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20170209 MGI PMID:20881014 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000536 hydroureter IAGP N RGD:5509061 20170209 MGI PMID:20881014 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20170209 MGI PMID:20881014 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000547 short limbs IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000561 adactyly IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20170209 MGI PMID:20215352 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000585 kinked tail IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000592 short tail IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000592 short tail IAGP N RGD:5509061 20170209 MGI PMID:20881014 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20170209 MGI PMID:15691760 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001194 dermatitis IAGP N RGD:5509061 20181122 MGI PMID:25902485 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20181122 MGI PMID:25902485 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20170209 MGI PMID:16085486 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001255 decreased body height IAGP N RGD:5509061 20170209 MGI PMID:23907671 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001258 decreased body length IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170209 MGI PMID:26234751 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170209 MGI PMID:15132997 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170209 MGI PMID:21484342 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001394 circling IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001505 hunched posture IAGP N RGD:5509061 20170209 MGI PMID:21484342 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001505 hunched posture IAGP N RGD:5509061 20170209 MGI PMID:23907671 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20170209 MGI PMID:19261698 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210722 MGI PMID:32991838 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20170209 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20240502 MGI PMID:38321001 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20240502 MGI PMID:38321001 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001926 female infertility IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20170209 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20170209 MGI PMID:24191021 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20181122 MGI PMID:25902485 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002083 premature death IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20170209 MGI PMID:11857796 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20170209 MGI PMID:15132997 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20170209 MGI PMID:16203988 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20170209 MGI PMID:16203988 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20170209 MGI PMID:16203988 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20170209 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170209 MGI PMID:19384968 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170209 MGI PMID:20806356 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170209 MGI PMID:21484342 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20170209 MGI PMID:15056615 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20170209 MGI PMID:15056615 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002256 abnormal laryngeal cartilage morphology IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20170209 MGI PMID:15056615 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20170209 MGI PMID:15056615 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20181122 MGI PMID:25902485 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20170209 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002639 micrognathia IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20170209 MGI PMID:22421045 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002711 decreased glucagon secretion IAGP N RGD:5509061 20170209 MGI PMID:18723011 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:16207837 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20170209 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20240104 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002785 absent Leydig cells IAGP N RGD:5509061 20170209 MGI PMID:15056615 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002785 absent Leydig cells IAGP N RGD:5509061 20170209 MGI PMID:16207837 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20181122 MGI PMID:25902485 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20170209 MGI PMID:11857796 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20170209 MGI PMID:16203988 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002898 absent cartilage IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20240502 MGI PMID:38321001 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20170209 MGI PMID:16207837 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20170209 MGI PMID:18723011 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20170209 MGI PMID:20215352 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003109 short femur IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003153 early eyelid opening IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20170209 MGI PMID:16085486 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003416 premature bone ossification IAGP N RGD:5509061 20170209 MGI PMID:23907671 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003417 premature endochondral bone ossification IAGP N RGD:5509061 20170209 MGI PMID:21484342 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003586 dilated ureter IAGP N RGD:5509061 20170209 MGI PMID:20881014 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003589 abnormal ureter physiology IAGP N RGD:5509061 20170209 MGI PMID:20881014 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003641 small lung IAGP N RGD:5509061 20170209 MGI PMID:24191021 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20170209 MGI PMID:16085486 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20170209 MGI PMID:15056615 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20170209 MGI PMID:16207837 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003853 dry skin IAGP N RGD:5509061 20181122 MGI PMID:25902485 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003854 abnormal forelimb stylopod morphology IAGP N RGD:5509061 20170209 MGI PMID:21484342 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003854 abnormal forelimb stylopod morphology IAGP N RGD:5509061 20170209 MGI PMID:23907671 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20170209 MGI PMID:21484342 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20170209 MGI PMID:23907671 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20170209 MGI PMID:20881014 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20170209 MGI PMID:18723011 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004204 absent stapes IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004318 absent incus IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004319 absent malleus IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004321 short sternum IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004343 small scapula IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004344 scapular bone hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:11857796 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004344 scapular bone hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004344 scapular bone hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:21484342 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004344 scapular bone hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:23907671 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004347 abnormal scapular spine morphology IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004351 short humerus IAGP N RGD:5509061 20170209 MGI PMID:21484342 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20170209 MGI PMID:11857796 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004355 short radius IAGP N RGD:5509061 20170209 MGI PMID:21484342 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004359 short ulna IAGP N RGD:5509061 20170209 MGI PMID:21484342 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004372 bowed fibula IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004374 bowed radius IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004374 bowed radius IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004493 dilated cochlea IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20230629 MGI PMID:34240584 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20230629 MGI PMID:34240584 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004506 abnormal pubis morphology IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004507 abnormal ischium morphology IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004592 small mandible IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20170209 MGI PMID:23236180 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004692 small pubis IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20170209 MGI PMID:20215352 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004862 small scala tympani IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0004880 lung cyst IAGP N RGD:5509061 20170209 MGI PMID:24191021 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:24191021 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20240502 MGI PMID:38321001 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20170209 MGI PMID:15056615 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005191 head tilt IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20170209 MGI PMID:21484342 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20170209 MGI PMID:15056615 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20170209 MGI PMID:11857796 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005307 head tossing IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005354 abnormal ilium morphology IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005356 positive geotaxis IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20170209 MGI PMID:26234751 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20170209 MGI PMID:18723011 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20170209 MGI PMID:20215352 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20170209 MGI PMID:20215352 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20240502 MGI PMID:38321001 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0005652 sex reversal IAGP N RGD:5509061 20170209 MGI PMID:15056615 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20170209 MGI PMID:19261698 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20170209 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0006121 calcified mitral valve IAGP N RGD:5509061 20170209 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20170209 MGI PMID:15056615 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20170209 MGI PMID:20881014 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0006328 nonsyndromic hearing impairment IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20170209 MGI PMID:24191021 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20170209 MGI PMID:22421045 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0006424 absent testis cords IAGP N RGD:5509061 20170209 MGI PMID:16207837 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20240502 MGI PMID:38321001 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20181122 MGI PMID:25902485 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20181122 MGI PMID:25902485 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20170209 MGI PMID:16203988 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20170209 MGI PMID:22421045 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0008309 dilated scala media IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0008384 absent nasal capsule IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0008385 absent basisphenoid bone IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0008386 absent styloid process IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20170209 MGI PMID:16203988 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20230629 MGI PMID:34240584 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20170209 MGI PMID:18723011 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0009139 failure of Mullerian duct regression IAGP N RGD:5509061 20170209 MGI PMID:16207837 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0009181 decreased pancreatic delta cell number IAGP N RGD:5509061 20170209 MGI PMID:18723011 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0009186 decreased PP cell number IAGP N RGD:5509061 20170209 MGI PMID:18723011 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0009247 meteorism IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20170209 MGI PMID:19201862 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0009759 abnormal hair follicle bulge morphology IAGP N RGD:5509061 20170209 MGI PMID:16085486 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20170209 MGI PMID:22421045 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20170209 MGI PMID:11857796 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0009910 bifurcated tongue IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0009915 absent hyoid bone lesser horns IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20170209 MGI PMID:26234751 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0010072 increased pruritus IAGP N RGD:5509061 20181122 MGI PMID:25902485 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0010116 abnormal primitive urogenital sinus morphology IAGP N RGD:5509061 20191219 MGI PMID:31669249 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20181122 MGI PMID:25902485 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20181122 MGI PMID:25902485 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0010587 conotruncal ridge hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0010684 abnormal hair follicle outer root sheath morphology IAGP N RGD:5509061 20170209 MGI PMID:16085486 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0010686 abnormal hair follicle matrix region morphology IAGP N RGD:5509061 20170209 MGI PMID:16085486 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20170209 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20170209 MGI PMID:24191021 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:24191021 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:11857796 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:16203988 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:15056615 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:15132997 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:24191021 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230420 MGI PMID:36343245 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:26234751 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:15056615 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:21484342 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:16207837 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:12414734 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011195 increased hair follicle apoptosis IAGP N RGD:5509061 20170209 MGI PMID:16085486 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011210 abnormal temporomandibular joint morphology IAGP N RGD:5509061 20170209 MGI PMID:19815519 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011426 abnormal ureter smooth muscle morphology IAGP N RGD:5509061 20170209 MGI PMID:20881014 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011480 impaired ureteric peristalsis IAGP N RGD:5509061 20170209 MGI PMID:20881014 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20170209 MGI PMID:26234751 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011648 thick heart valve cusps IAGP N RGD:5509061 20240104 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20170209 MGI PMID:24191021 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20170209 MGI PMID:26234751 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0012243 decreased hepatoblast number IAGP N RGD:5509061 20240502 MGI PMID:38321001 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0012756 impaired cranial neural crest cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:16207837 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0013013 abnormal trunk neural crest cell morphology IAGP N RGD:5509061 20170209 MGI PMID:15691760 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0013014 increased trunk neural crest cell apoptosis IAGP N RGD:5509061 20170209 MGI PMID:15691760 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20170209 MGI PMID:26234751 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0021210 bilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:11371614 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0030162 absent hyoid bone body IAGP N RGD:5509061 20171005 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0030258 small mandibular condyloid process IAGP N RGD:5509061 20171019 MGI PMID:19815519 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0030259 mandibular condyloid process hypoplasia IAGP N RGD:5509061 20210722 MGI PMID:32991838 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0030588 decreased pancreatic alpha cell mass IAGP N RGD:5509061 20180614 MGI PMID:18723011 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0030835 abnormal ankle joint morphology IAGP N RGD:5509061 20181025 MGI PMID:20215352 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0030868 absent thyroid cartilage IAGP N RGD:5509061 20181101 MGI PMID:12878728 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0031549 abnormal heart valve development IAGP N RGD:5509061 20240104 MGI PMID:17350610 1322514 Sox9 SRY (sex determining region Y)-box 9 gene MP:0031550 abnormal atrioventricular valve development IAGP N RGD:5509061 20240104 MGI PMID:17350610 1322519 Itga9 integrin alpha 9 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10866676 1322519 Itga9 integrin alpha 9 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:22772469 1322519 Itga9 integrin alpha 9 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10866676 1322519 Itga9 integrin alpha 9 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:22772469 1322519 Itga9 integrin alpha 9 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:22772469 1322519 Itga9 integrin alpha 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18633440 1322519 Itga9 integrin alpha 9 gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20141003 MGI PMID:10866676 1322519 Itga9 integrin alpha 9 gene MP:0003660 chylothorax IAGP N RGD:5509061 20141003 MGI PMID:10866676 1322519 Itga9 integrin alpha 9 gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:18633440 1322519 Itga9 integrin alpha 9 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:18633440 1322519 Itga9 integrin alpha 9 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18633440 1322519 Itga9 integrin alpha 9 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10866676 1322519 Itga9 integrin alpha 9 gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:18633440 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16199873 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:16199873 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:16199873 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16199873 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19753101 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19753101 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15044949 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19753101 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:6855886 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16199873 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16199873 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19753101 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:19753101 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:6855886 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:6855886 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0002213 true hermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:6855886 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16199873 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16199873 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16199873 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:19753101 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:6855886 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0002996 ovotestis IAGP N RGD:5509061 20141003 MGI PMID:19753101 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0002996 ovotestis IAGP N RGD:5509061 20141003 MGI PMID:6855886 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:16199873 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:16199873 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:19753101 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:16199873 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:19753101 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:23102580 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:15044949 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0005652 sex reversal IAGP N RGD:5509061 20141003 MGI PMID:6855886 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0006418 abnormal testis cord formation IAGP N RGD:5509061 20141003 MGI PMID:19753101 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0006424 absent testis cords IAGP N RGD:5509061 20141003 MGI PMID:19753101 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:16199873 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15044949 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:16199873 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15044949 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16199873 1322521 Map3k4 mitogen-activated protein kinase kinase kinase 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19753101 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20230601 MGI 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20231123 MGI PMID:36748836 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20231123 MGI PMID:36748836 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20231123 MGI PMID:36748836 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20221215 MGI 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20220519 MGI 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20231123 MGI PMID:36748836 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20170105 MGI 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20231123 MGI PMID:36748836 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20231123 MGI PMID:36748836 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20231123 MGI PMID:36748836 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20231123 MGI PMID:36748836 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1322526 Lyplal1 lysophospholipase-like 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20231123 MGI PMID:36748836 1322528 Tdrkh tudor and KH domain containing protein gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23714778 1322528 Tdrkh tudor and KH domain containing protein gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1322528 Tdrkh tudor and KH domain containing protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23714778 1322528 Tdrkh tudor and KH domain containing protein gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:23714778 1322528 Tdrkh tudor and KH domain containing protein gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:23714778 1322528 Tdrkh tudor and KH domain containing protein gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23714778 1322528 Tdrkh tudor and KH domain containing protein gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23714778 1322528 Tdrkh tudor and KH domain containing protein gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:23714778 1322528 Tdrkh tudor and KH domain containing protein gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:23714778 1322528 Tdrkh tudor and KH domain containing protein gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:23714778 1322528 Tdrkh tudor and KH domain containing protein gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1322530 Mkrn3 makorin, ring finger protein, 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230601 MGI PMID:34692086 1322530 Mkrn3 makorin, ring finger protein, 3 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20230601 MGI PMID:34692086 1322530 Mkrn3 makorin, ring finger protein, 3 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20230601 MGI PMID:34692086 1322530 Mkrn3 makorin, ring finger protein, 3 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20230601 MGI PMID:34692086 1322530 Mkrn3 makorin, ring finger protein, 3 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20230601 MGI PMID:34692086 1322530 Mkrn3 makorin, ring finger protein, 3 gene MP:0003378 early sexual maturation IAGP N RGD:5509061 20230601 MGI PMID:34692086 1322530 Mkrn3 makorin, ring finger protein, 3 gene MP:0008994 early vaginal opening IAGP N RGD:5509061 20230601 MGI PMID:34692086 1322530 Mkrn3 makorin, ring finger protein, 3 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1322530 Mkrn3 makorin, ring finger protein, 3 gene MP:0031399 early balanopreputial separation IAGP N RGD:5509061 20230601 MGI PMID:34692086 1322533 Peli1 pellino 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230601 MGI 1322533 Peli1 pellino 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210805 MGI 1322533 Peli1 pellino 1 gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:22902624 1322533 Peli1 pellino 1 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22902624 1322533 Peli1 pellino 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210805 MGI 1322533 Peli1 pellino 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210805 MGI 1322533 Peli1 pellino 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22902624 1322533 Peli1 pellino 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1322533 Peli1 pellino 1 gene MP:0002175 decreased brain weight IEA N RGD:5509061 20210805 MGI 1322533 Peli1 pellino 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:22902624 1322533 Peli1 pellino 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210805 MGI 1322533 Peli1 pellino 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1322533 Peli1 pellino 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19734906 1322533 Peli1 pellino 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210805 MGI 1322533 Peli1 pellino 1 gene MP:0008463 abnormal peripheral lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:22902624 1322533 Peli1 pellino 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19734906 1322533 Peli1 pellino 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22902624 1322533 Peli1 pellino 1 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:22902624 1322533 Peli1 pellino 1 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22902624 1322533 Peli1 pellino 1 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20141003 MGI PMID:19734906 1322533 Peli1 pellino 1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:19734906 1322533 Peli1 pellino 1 gene MP:0008648 decreased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:19734906 1322533 Peli1 pellino 1 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:22902624 1322533 Peli1 pellino 1 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:19734906 1322533 Peli1 pellino 1 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:22902624 1322533 Peli1 pellino 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:22902624 1322533 Peli1 pellino 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:19734906 1322533 Peli1 pellino 1 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19734906 1322533 Peli1 pellino 1 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19734906 1322533 Peli1 pellino 1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22902624 1322535 Surf4 surfeit gene 4 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1322535 Surf4 surfeit gene 4 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20211223 MGI PMID:33186557 1322535 Surf4 surfeit gene 4 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20211223 MGI PMID:33186557 1322535 Surf4 surfeit gene 4 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1322535 Surf4 surfeit gene 4 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20211223 MGI PMID:33186557 1322535 Surf4 surfeit gene 4 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20211223 MGI PMID:33186557 1322535 Surf4 surfeit gene 4 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:31978056 1322535 Surf4 surfeit gene 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1322536 Pabpc6 poly(A) binding protein, cytoplasmic 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240801 MGI PMID:38281153 1322538 Trim15 tripartite motif-containing 15 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20200514 MGI 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20200514 MGI 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322542 Tm7sf2 transmembrane 7 superfamily member 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17403717 1322549 Emilin1 elastin microfibril interfacer 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14701737 1322549 Emilin1 elastin microfibril interfacer 1 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20160414 MGI PMID:25658937 1322549 Emilin1 elastin microfibril interfacer 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20160414 MGI PMID:25658937 1322549 Emilin1 elastin microfibril interfacer 1 gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:14701737 1322549 Emilin1 elastin microfibril interfacer 1 gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:14701737 1322549 Emilin1 elastin microfibril interfacer 1 gene MP:0012356 increased prothrombin time IAGP N RGD:5509061 20160414 MGI PMID:25658937 1322550 Boll boule homolog, RNA binding protein gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20335278 1322550 Boll boule homolog, RNA binding protein gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:20335278 1322550 Boll boule homolog, RNA binding protein gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:20335278 1322550 Boll boule homolog, RNA binding protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20335278 1322550 Boll boule homolog, RNA binding protein gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20335278 1322550 Boll boule homolog, RNA binding protein gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:20335278 1322550 Boll boule homolog, RNA binding protein gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:20335278 1322550 Boll boule homolog, RNA binding protein gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20335278 1322550 Boll boule homolog, RNA binding protein gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20335278 1322550 Boll boule homolog, RNA binding protein gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:20335278 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23064362 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23064362 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0000676 abnormal body water content IAGP N RGD:5509061 20141003 MGI PMID:17908936 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:23064362 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:17908936 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:23064362 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:23064362 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:23064362 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:17908936 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0001208 blistering IAGP N RGD:5509061 20170309 MGI PMID:17908936 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:23064362 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17908936 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0001304 cataract IEA N RGD:5509061 20220519 MGI 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:23064362 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:17908936 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17908936 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0002989 small kidney IEA N RGD:5509061 20220519 MGI 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:17908936 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:17908936 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:17908936 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23064362 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20141003 MGI PMID:17908936 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17908936 1322553 Il36rn interleukin 36 receptor antagonist gene MP:0012572 increased susceptibility to chemically induced skin inflammation IAGP N RGD:5509061 20191114 MGI PMID:29554104 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322556 Smc6 structural maintenance of chromosomes 6 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20151126 MGI PMID:23518413 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:16289463 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:21549111 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:16934545 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:16934545 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21549111 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:21549111 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20111116 MGI 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001263 weight loss IEA N RGD:5509061 20111116 MGI 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16934545 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001288 abnormal lens induction IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:16934545 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:16934545 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002252 abnormal oropharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:16934545 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0004605 abnormal vertebral lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:18789316 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0004711 persistence of notochord tissue IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0004874 abnormal timing of postnatal eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0005226 abnormal vertebral arch development IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16934545 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0006086 decreased body mass index IEA N RGD:5509061 20111116 MGI 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:21549111 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0009323 abnormal spleen development IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0009524 absent submandibular gland IAGP N RGD:5509061 20150226 MGI PMID:16289463 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0009576 oral atresia IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0009880 decreased mouth size IAGP N RGD:5509061 20141003 MGI PMID:16289463 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:21549111 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0009905 absent tongue IAGP N RGD:5509061 20141003 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:16934545 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0010335 fused first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0010335 fused first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:21549111 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:16934545 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:16934545 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:16934545 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21549111 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16934545 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18789316 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0013541 abnormal submandibular gland development IAGP N RGD:5509061 20150226 MGI PMID:16289463 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0013790 single external naris IAGP N RGD:5509061 20150611 MGI PMID:14681194 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0013790 single external naris IAGP N RGD:5509061 20150611 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0014277 alobar holoprosencephaly IAGP N RGD:5509061 20230810 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0021190 decreased bone mineral density of lumbar vertebrae IAGP N RGD:5509061 20220915 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0030268 agnathia IAGP N RGD:5509061 20171214 MGI PMID:15013800 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0030279 thin neurocranium IAGP N RGD:5509061 20171102 MGI PMID:12665593 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0030985 decreased circulating osteocalcin level IAGP N RGD:5509061 20201001 MGI PMID:16934545 1322558 Twsg1 twisted gastrulation BMP signaling modulator 1 gene MP:0031109 subarachnoid hemorrhage IAGP N RGD:5509061 20200917 MGI PMID:12665593 1322561 Vcl vinculin gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15331426 1322561 Vcl vinculin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20644727 1322561 Vcl vinculin gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:20644727 1322561 Vcl vinculin gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:20644727 1322561 Vcl vinculin gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:20644727 1322561 Vcl vinculin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20644727 1322561 Vcl vinculin gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:15331426 1322561 Vcl vinculin gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:20644727 1322561 Vcl vinculin gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15331426 1322561 Vcl vinculin gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:15331426 1322561 Vcl vinculin gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:15331426 1322561 Vcl vinculin gene MP:0010559 heart block IAGP N RGD:5509061 20141003 MGI PMID:17785437 1322561 Vcl vinculin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20644727 1322561 Vcl vinculin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:20644727 1322561 Vcl vinculin gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0012176 abnormal head development IAGP N RGD:5509061 20171214 MGI PMID:20644727 1322561 Vcl vinculin gene MP:0012250 absent heart valves IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0012677 absent brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:20644727 1322561 Vcl vinculin gene MP:0012677 absent brain ventricles IAGP N RGD:5509061 20161103 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20644727 1322561 Vcl vinculin gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0013164 abnormal forelimb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0013166 small forelimb buds IAGP N RGD:5509061 20141003 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0013227 small brain ventricles IAGP N RGD:5509061 20161103 MGI PMID:9486805 1322561 Vcl vinculin gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15331426 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0001588 abnormal hemoglobin IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:21788586 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0003717 pallor IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:21788586 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:21788586 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21788586 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21788586 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21788586 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322568 Abcb10 ATP-binding cassette, sub-family B member 10 gene MP:0013657 abnormal blood cell morphology IAGP N RGD:5509061 20160304 MGI PMID:24421385 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0000601 small liver IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20181227 MGI 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0001889 delayed brain development IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0002188 small heart IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0002989 small kidney IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0003641 small lung IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0010545 abnormal heart layer morphology IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0012269 nuchal edema IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322574 Cdk13 cyclin dependent kinase 13 gene MP:0013580 abnormal nasal gland morphology IAGP N RGD:5509061 20200910 MGI PMID:31440507 1322581 Rel reticuloendotheliosis oncogene gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20210128 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:10518539 1322581 Rel reticuloendotheliosis oncogene gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:10518539 1322581 Rel reticuloendotheliosis oncogene gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15199130 1322581 Rel reticuloendotheliosis oncogene gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:15199130 1322581 Rel reticuloendotheliosis oncogene gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:15199130 1322581 Rel reticuloendotheliosis oncogene gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0000745 tremors IEA N RGD:5509061 20160421 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15199130 1322581 Rel reticuloendotheliosis oncogene gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:15199130 1322581 Rel reticuloendotheliosis oncogene gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:15199130 1322581 Rel reticuloendotheliosis oncogene gene MP:0001284 absent vibrissae IEA N RGD:5509061 20160421 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0001606 impaired hematopoiesis IEA N RGD:5509061 20161201 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10518539 1322581 Rel reticuloendotheliosis oncogene gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15199130 1322581 Rel reticuloendotheliosis oncogene gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:11869686 1322581 Rel reticuloendotheliosis oncogene gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:7649478 1322581 Rel reticuloendotheliosis oncogene gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:7649478 1322581 Rel reticuloendotheliosis oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0002145 abnormal T cell differentiation IEA N RGD:5509061 20190418 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14568969 1322581 Rel reticuloendotheliosis oncogene gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:14568969 1322581 Rel reticuloendotheliosis oncogene gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:9003785 1322581 Rel reticuloendotheliosis oncogene gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14568969 1322581 Rel reticuloendotheliosis oncogene gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:10586083 1322581 Rel reticuloendotheliosis oncogene gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15199130 1322581 Rel reticuloendotheliosis oncogene gene MP:0002814 hyperchromasia IAGP N RGD:5509061 20141003 MGI PMID:10518539 1322581 Rel reticuloendotheliosis oncogene gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:10221648 1322581 Rel reticuloendotheliosis oncogene gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:12235116 1322581 Rel reticuloendotheliosis oncogene gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:7649478 1322581 Rel reticuloendotheliosis oncogene gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:9003785 1322581 Rel reticuloendotheliosis oncogene gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15199130 1322581 Rel reticuloendotheliosis oncogene gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:9862367 1322581 Rel reticuloendotheliosis oncogene gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15818410 1322581 Rel reticuloendotheliosis oncogene gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10518539 1322581 Rel reticuloendotheliosis oncogene gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12235116 1322581 Rel reticuloendotheliosis oncogene gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:14568969 1322581 Rel reticuloendotheliosis oncogene gene MP:0004978 decreased B-1 B cell number IEA N RGD:5509061 20161201 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10586083 1322581 Rel reticuloendotheliosis oncogene gene MP:0005015 increased T cell number IEA N RGD:5509061 20161201 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9003785 1322581 Rel reticuloendotheliosis oncogene gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:10221648 1322581 Rel reticuloendotheliosis oncogene gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7649478 1322581 Rel reticuloendotheliosis oncogene gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9862367 1322581 Rel reticuloendotheliosis oncogene gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10221648 1322581 Rel reticuloendotheliosis oncogene gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12235116 1322581 Rel reticuloendotheliosis oncogene gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7649478 1322581 Rel reticuloendotheliosis oncogene gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12235116 1322581 Rel reticuloendotheliosis oncogene gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14568969 1322581 Rel reticuloendotheliosis oncogene gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14568969 1322581 Rel reticuloendotheliosis oncogene gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20161201 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20161201 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0008076 abnormal CD4-positive T cell differentiation IEA N RGD:5509061 20190418 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20161201 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20161201 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12235116 1322581 Rel reticuloendotheliosis oncogene gene MP:0008093 abnormal memory B cell number IAGP N RGD:5509061 20141003 MGI PMID:9862367 1322581 Rel reticuloendotheliosis oncogene gene MP:0008112 abnormal monocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:10518539 1322581 Rel reticuloendotheliosis oncogene gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:7649478 1322581 Rel reticuloendotheliosis oncogene gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:7649478 1322581 Rel reticuloendotheliosis oncogene gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:7649478 1322581 Rel reticuloendotheliosis oncogene gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:7649478 1322581 Rel reticuloendotheliosis oncogene gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:11869686 1322581 Rel reticuloendotheliosis oncogene gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:10518539 1322581 Rel reticuloendotheliosis oncogene gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0010842 decreased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20161201 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0010845 decreased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15199130 1322581 Rel reticuloendotheliosis oncogene gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10518539 1322581 Rel reticuloendotheliosis oncogene gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0014347 increased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:9529314 1322581 Rel reticuloendotheliosis oncogene gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20161201 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20190418 MGI 1322581 Rel reticuloendotheliosis oncogene gene MP:0021086 decreased DNA replication IAGP N RGD:5509061 20220310 MGI PMID:9862367 1322581 Rel reticuloendotheliosis oncogene gene MP:0030582 abnormal hair follicle placode formation IAGP N RGD:5509061 20180614 MGI PMID:15199130 1322584 Bhlha9 basic helix-loop-helix family, member a9 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141127 MGI PMID:24852374 1322584 Bhlha9 basic helix-loop-helix family, member a9 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141127 MGI PMID:24852374 1322584 Bhlha9 basic helix-loop-helix family, member a9 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20181227 MGI 1322584 Bhlha9 basic helix-loop-helix family, member a9 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20181227 MGI 1322584 Bhlha9 basic helix-loop-helix family, member a9 gene MP:0009874 abnormal interdigital cell death IAGP N RGD:5509061 20141127 MGI PMID:24852374 1322586 Myl9 myosin, light polypeptide 9, regulatory gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20210819 MGI PMID:33424621 1322586 Myl9 myosin, light polypeptide 9, regulatory gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20210819 MGI PMID:33424621 1322586 Myl9 myosin, light polypeptide 9, regulatory gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210819 MGI PMID:33424621 1322586 Myl9 myosin, light polypeptide 9, regulatory gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20210819 MGI PMID:33424621 1322586 Myl9 myosin, light polypeptide 9, regulatory gene MP:0001265 decreased body size IAGP N RGD:5509061 20210819 MGI PMID:33424621 1322586 Myl9 myosin, light polypeptide 9, regulatory gene MP:0002083 premature death IAGP N RGD:5509061 20210819 MGI PMID:33424621 1322586 Myl9 myosin, light polypeptide 9, regulatory gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20210819 MGI PMID:33424621 1322586 Myl9 myosin, light polypeptide 9, regulatory gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20210819 MGI PMID:33424621 1322586 Myl9 myosin, light polypeptide 9, regulatory gene MP:0004006 impaired contractility of jejunal smooth muscle IAGP N RGD:5509061 20210819 MGI PMID:33424621 1322586 Myl9 myosin, light polypeptide 9, regulatory gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20210819 MGI PMID:33424621 1322586 Myl9 myosin, light polypeptide 9, regulatory gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20210819 MGI PMID:33424621 1322586 Myl9 myosin, light polypeptide 9, regulatory gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210819 MGI PMID:33424621 1322586 Myl9 myosin, light polypeptide 9, regulatory gene MP:0011503 distended jejunum IAGP N RGD:5509061 20210819 MGI PMID:33424621 1322586 Myl9 myosin, light polypeptide 9, regulatory gene MP:0011881 distended duodenum IAGP N RGD:5509061 20210819 MGI PMID:33424621 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210128 MGI 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210128 MGI 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0004262 abnormal physical strength IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0008913 weaving IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19196968 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20220519 MGI 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0010935 increased airway resistance IEA N RGD:5509061 20211021 MGI 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0011044 increased lung elastance IEA N RGD:5509061 20211021 MGI 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0011047 increased lung tissue damping IEA N RGD:5509061 20210128 MGI 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1322591 Ltn1 listerin E3 ubiquitin protein ligase 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20240523 MGI 1322593 Pdcd6 programmed cell death 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12024023 1322597 Dhrs7b dehydrogenase/reductase 7B gene MP:0000749 muscle degeneration IEA N RGD:5509061 20141003 MGI 1322597 Dhrs7b dehydrogenase/reductase 7B gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1322597 Dhrs7b dehydrogenase/reductase 7B gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1322597 Dhrs7b dehydrogenase/reductase 7B gene MP:0003644 thymus atrophy IEA N RGD:5509061 20141003 MGI 1322597 Dhrs7b dehydrogenase/reductase 7B gene MP:0004545 enlarged esophagus IEA N RGD:5509061 20141003 MGI 1322597 Dhrs7b dehydrogenase/reductase 7B gene MP:0010788 stomach hypoplasia IEA N RGD:5509061 20141003 MGI 1322597 Dhrs7b dehydrogenase/reductase 7B gene MP:0011085 postnatal lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 1322597 Dhrs7b dehydrogenase/reductase 7B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1322600 Rsf1 remodeling and spacing factor 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20201022 MGI 1322600 Rsf1 remodeling and spacing factor 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1322600 Rsf1 remodeling and spacing factor 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20191107 MGI PMID:30348983 1322600 Rsf1 remodeling and spacing factor 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1322600 Rsf1 remodeling and spacing factor 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20191107 MGI PMID:30348983 1322600 Rsf1 remodeling and spacing factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1322603 Dlgap5 DLG associated protein 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18676373 1322603 Dlgap5 DLG associated protein 5 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:18676373 1322608 Slc35c2 solute carrier family 35, member C2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20241010 MGI PMID:38270391 1322608 Slc35c2 solute carrier family 35, member C2 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20181227 MGI 1322608 Slc35c2 solute carrier family 35, member C2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20241010 MGI PMID:38270391 1322608 Slc35c2 solute carrier family 35, member C2 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20241010 MGI PMID:38270391 1322608 Slc35c2 solute carrier family 35, member C2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20241010 MGI PMID:38270391 1322608 Slc35c2 solute carrier family 35, member C2 gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20241010 MGI PMID:38270391 1322608 Slc35c2 solute carrier family 35, member C2 gene MP:0004648 decreased thoracic vertebrae number IAGP N RGD:5509061 20241010 MGI PMID:38270391 1322608 Slc35c2 solute carrier family 35, member C2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210826 MGI 1322608 Slc35c2 solute carrier family 35, member C2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20241010 MGI PMID:38270391 1322608 Slc35c2 solute carrier family 35, member C2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20241010 MGI PMID:38270391 1322608 Slc35c2 solute carrier family 35, member C2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210826 MGI 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:16728642 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22573816 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:12378523 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:12378523 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:22573816 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:22573816 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12378523 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23945236 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23945236 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:22573816 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:23945236 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:22573816 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:16728642 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:23945236 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12378523 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16728642 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:16728642 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:22573816 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:23945236 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:22573816 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:14707112 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23945236 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:23945236 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23945236 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:22573816 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:23945236 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0012072 decreased susceptibility to osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:22573816 1322611 Hivep3 human immunodeficiency virus type I enhancer binding protein 3 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:23945236 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0003708 binucleate IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0004575 small limb buds IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20141003 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20141003 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0009852 increased Sertoli cell phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20160728 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20230615 MGI PMID:25521379 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220811 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20220811 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220811 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0031373 abnormal manchette perinuclear ring morphology IAGP N RGD:5509061 20220407 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0031375 abnormal manchette disassembly IAGP N RGD:5509061 20220407 MGI PMID:22654669 1322616 Katnb1 katanin p80 (WD40-containing) subunit B 1 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20220428 MGI PMID:22654669 1322618 Slx9 SLX9 ribosome biogenesis factor gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230720 MGI 1322622 Mmgt2 membrane magnesium transporter 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 1322622 Mmgt2 membrane magnesium transporter 2 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1322622 Mmgt2 membrane magnesium transporter 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20230601 MGI 1322622 Mmgt2 membrane magnesium transporter 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1322628 Ltv1 LTV1 ribosome biogenesis factor gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1322628 Ltv1 LTV1 ribosome biogenesis factor gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240919 MGI 1322628 Ltv1 LTV1 ribosome biogenesis factor gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241017 MGI 1322628 Ltv1 LTV1 ribosome biogenesis factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1322628 Ltv1 LTV1 ribosome biogenesis factor gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20240919 MGI 1322631 Tex15 testis expressed gene 15 meiosis and synapsis associated gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18283110 1322631 Tex15 testis expressed gene 15 meiosis and synapsis associated gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18283110 1322631 Tex15 testis expressed gene 15 meiosis and synapsis associated gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18283110 1322631 Tex15 testis expressed gene 15 meiosis and synapsis associated gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:18283110 1322631 Tex15 testis expressed gene 15 meiosis and synapsis associated gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18283110 1322631 Tex15 testis expressed gene 15 meiosis and synapsis associated gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:18283110 1322639 Ippk inositol 1,3,4,5,6-pentakisphosphate 2-kinase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20190502 MGI 1322639 Ippk inositol 1,3,4,5,6-pentakisphosphate 2-kinase gene MP:0000274 enlarged heart IEA N RGD:5509061 20190502 MGI 1322639 Ippk inositol 1,3,4,5,6-pentakisphosphate 2-kinase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221103 MGI 1322639 Ippk inositol 1,3,4,5,6-pentakisphosphate 2-kinase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20221103 MGI 1322639 Ippk inositol 1,3,4,5,6-pentakisphosphate 2-kinase gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15939868 1322639 Ippk inositol 1,3,4,5,6-pentakisphosphate 2-kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322639 Ippk inositol 1,3,4,5,6-pentakisphosphate 2-kinase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 1322641 Alg9 ALG9 alpha-1,2-mannosyltransferase gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1322641 Alg9 ALG9 alpha-1,2-mannosyltransferase gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1322641 Alg9 ALG9 alpha-1,2-mannosyltransferase gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1322641 Alg9 ALG9 alpha-1,2-mannosyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322641 Alg9 ALG9 alpha-1,2-mannosyltransferase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1322642 Mcrip2 MAPK regulated corepressor interacting protein 2 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20220120 MGI PMID:34088848 1322642 Mcrip2 MAPK regulated corepressor interacting protein 2 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20220120 MGI PMID:34088848 1322642 Mcrip2 MAPK regulated corepressor interacting protein 2 gene MP:0020520 whitened brown adipose tissue morphology IAGP N RGD:5509061 20220120 MGI PMID:34088848 1322646 Foxh1 forkhead box H1 gene MP:0000024 lowered ear position IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0000087 absent mandible IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15363409 1322646 Foxh1 forkhead box H1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:15363409 1322646 Foxh1 forkhead box H1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15363409 1322646 Foxh1 forkhead box H1 gene MP:0000433 microcephaly IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0000477 abnormal intestine morphology IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0000508 right-sided isomerism IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0000650 mesocardia IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0000690 absent spleen IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:11358869 1322646 Foxh1 forkhead box H1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11358869 1322646 Foxh1 forkhead box H1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:15363409 1322646 Foxh1 forkhead box H1 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0001890 anencephaly IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25511461 1322646 Foxh1 forkhead box H1 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:15363409 1322646 Foxh1 forkhead box H1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15363409 1322646 Foxh1 forkhead box H1 gene MP:0003104 acrania IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0003388 absent pericardium IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0003872 absent heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15363409 1322646 Foxh1 forkhead box H1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15363409 1322646 Foxh1 forkhead box H1 gene MP:0003924 diaphragmatic hernia IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11358869 1322646 Foxh1 forkhead box H1 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0004113 abnormal aortic arch morphology IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0004133 heterotaxia IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0004158 right aortic arch IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:11358869 1322646 Foxh1 forkhead box H1 gene MP:0004733 abnormal thoracic cavity morphology IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:11358869 1322646 Foxh1 forkhead box H1 gene MP:0005163 cyclopia IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15363409 1322646 Foxh1 forkhead box H1 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11358869 1322646 Foxh1 forkhead box H1 gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:15363409 1322646 Foxh1 forkhead box H1 gene MP:0006290 proboscis IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:11358869 1322646 Foxh1 forkhead box H1 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:11358869 1322646 Foxh1 forkhead box H1 gene MP:0009880 decreased mouth size IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0010406 common atrium IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0010431 atrial situs inversus IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0010432 common ventricle IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0010446 heart left ventricle hypoplasia IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0010466 vascular ring IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0010487 abnormal right subclavian artery morphology IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0010668 abnormal hepatic portal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11358869 1322646 Foxh1 forkhead box H1 gene MP:0011250 abdominal situs ambiguus IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0011253 situs inversus with levocardia IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0011323 abnormal renal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0011569 abnormal azygos vein morphology IAGP N RGD:5509061 20141003 MGI PMID:12642485 1322646 Foxh1 forkhead box H1 gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0011668 double outlet right ventricle, Taussig bing type IEA N RGD:5509061 20150226 MGI 1322646 Foxh1 forkhead box H1 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:11358869 1322646 Foxh1 forkhead box H1 gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:11358869 1322646 Foxh1 forkhead box H1 gene MP:0012165 absent neural folds IAGP N RGD:5509061 20141003 MGI PMID:11358869 1322646 Foxh1 forkhead box H1 gene MP:0012276 absent prechordal mesoderm IAGP N RGD:5509061 20141003 MGI PMID:11358869 1322646 Foxh1 forkhead box H1 gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:11358869 1322646 Foxh1 forkhead box H1 gene MP:0012739 abnormal anterior primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:11358869 1322646 Foxh1 forkhead box H1 gene MP:0030324 abnormal anterior head development IAGP N RGD:5509061 20180118 MGI PMID:11358869 1322648 Prss53 serine protease 53 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20200402 MGI 1322648 Prss53 serine protease 53 gene MP:0001257 increased body length IEA N RGD:5509061 20200402 MGI 1322648 Prss53 serine protease 53 gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20201022 MGI 1322648 Prss53 serine protease 53 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20181227 MGI 1322648 Prss53 serine protease 53 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1322648 Prss53 serine protease 53 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1322648 Prss53 serine protease 53 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 1322648 Prss53 serine protease 53 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20181227 MGI 1322652 Dnttip1 deoxynucleotidyltransferase, terminal, interacting protein 1 gene MP:0000215 absent erythrocytes IAGP N RGD:5509061 20201224 MGI PMID:32591534 1322652 Dnttip1 deoxynucleotidyltransferase, terminal, interacting protein 1 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20201224 MGI PMID:32591534 1322652 Dnttip1 deoxynucleotidyltransferase, terminal, interacting protein 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20201224 MGI PMID:32591534 1322652 Dnttip1 deoxynucleotidyltransferase, terminal, interacting protein 1 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20201224 MGI PMID:32591534 1322652 Dnttip1 deoxynucleotidyltransferase, terminal, interacting protein 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20201224 MGI PMID:32591534 1322652 Dnttip1 deoxynucleotidyltransferase, terminal, interacting protein 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20201224 MGI PMID:32591534 1322652 Dnttip1 deoxynucleotidyltransferase, terminal, interacting protein 1 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20220811 MGI 1322652 Dnttip1 deoxynucleotidyltransferase, terminal, interacting protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20201224 MGI PMID:32591534 1322652 Dnttip1 deoxynucleotidyltransferase, terminal, interacting protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322655 Prss35 serine protease 35 gene MP:0000160 kyphosis IEA N RGD:5509061 20231207 MGI 1322655 Prss35 serine protease 35 gene MP:0000162 lordosis IEA N RGD:5509061 20220811 MGI 1322655 Prss35 serine protease 35 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1322655 Prss35 serine protease 35 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1322655 Prss35 serine protease 35 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1322655 Prss35 serine protease 35 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1322655 Prss35 serine protease 35 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 1322655 Prss35 serine protease 35 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 1322655 Prss35 serine protease 35 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1322655 Prss35 serine protease 35 gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1322655 Prss35 serine protease 35 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1322655 Prss35 serine protease 35 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1322655 Prss35 serine protease 35 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180705 MGI PMID:23451081 1322655 Prss35 serine protease 35 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210826 MGI 1322655 Prss35 serine protease 35 gene MP:0009709 hydrometra IEA N RGD:5509061 20210826 MGI 1322657 Champ1 chromosome alignment maintaining phosphoprotein 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20230601 MGI 1322657 Champ1 chromosome alignment maintaining phosphoprotein 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1322657 Champ1 chromosome alignment maintaining phosphoprotein 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1322657 Champ1 chromosome alignment maintaining phosphoprotein 1 gene MP:0000692 small spleen IEA N RGD:5509061 20230119 MGI 1322657 Champ1 chromosome alignment maintaining phosphoprotein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 1322657 Champ1 chromosome alignment maintaining phosphoprotein 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1322657 Champ1 chromosome alignment maintaining phosphoprotein 1 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20230601 MGI 1322657 Champ1 chromosome alignment maintaining phosphoprotein 1 gene MP:0001785 edema IEA N RGD:5509061 20230601 MGI 1322657 Champ1 chromosome alignment maintaining phosphoprotein 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1322657 Champ1 chromosome alignment maintaining phosphoprotein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1322659 Ttc5 tetratricopeptide repeat domain 5 gene MP:0010052 increased grip strength IEA N RGD:5509061 20231207 MGI 1322664 Cd109 CD109 antigen gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:22846721 1322664 Cd109 CD109 antigen gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22846721 1322664 Cd109 CD109 antigen gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:22846721 1322664 Cd109 CD109 antigen gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22846721 1322664 Cd109 CD109 antigen gene MP:0001284 absent vibrissae IEA N RGD:5509061 20230601 MGI 1322664 Cd109 CD109 antigen gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:22846721 1322664 Cd109 CD109 antigen gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:22846721 1322664 Cd109 CD109 antigen gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:22846721 1322664 Cd109 CD109 antigen gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20221215 MGI 1322664 Cd109 CD109 antigen gene MP:0009612 thick epidermis suprabasal layer IAGP N RGD:5509061 20141003 MGI PMID:22846721 1322664 Cd109 CD109 antigen gene MP:0009715 thick epidermis stratum basale IAGP N RGD:5509061 20141003 MGI PMID:22846721 1322664 Cd109 CD109 antigen gene MP:0009794 sebaceous gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22846721 1322664 Cd109 CD109 antigen gene MP:0010678 abnormal skin adnexa morphology IAGP N RGD:5509061 20141003 MGI PMID:22846721 1322664 Cd109 CD109 antigen gene MP:0010682 abnormal hair follicle infundibulum morphology IAGP N RGD:5509061 20141003 MGI PMID:22846721 1322664 Cd109 CD109 antigen gene MP:0010699 dilated hair follicle IAGP N RGD:5509061 20141003 MGI PMID:22846721 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20240808 MGI PMID:38767782 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20240808 MGI PMID:38301772 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20240808 MGI PMID:38301772 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20240808 MGI PMID:38767782 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20240808 MGI PMID:38301772 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20240808 MGI PMID:38301772 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20240808 MGI PMID:38767782 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20240808 MGI PMID:38767782 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20240808 MGI PMID:38301772 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20240808 MGI PMID:38301772 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0012006 abnormal hippocampus physiology IAGP N RGD:5509061 20240808 MGI PMID:38301772 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240808 MGI PMID:38301772 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0014369 enhanced spatial working memory IAGP N RGD:5509061 20240808 MGI PMID:38301772 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0020870 decreased thigmotaxis IAGP N RGD:5509061 20240808 MGI PMID:38301772 1322666 Dcaf11 DDB1 and CUL4 associated factor 11 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20240808 MGI PMID:38301772 1322668 Spag9 sperm associated antigen 9 gene MP:0000371 diluted coat color IEA N RGD:5509061 20111116 MGI 1322668 Spag9 sperm associated antigen 9 gene MP:0001189 absent skin pigmentation IEA N RGD:5509061 20111116 MGI 1322668 Spag9 sperm associated antigen 9 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:18574703 1322668 Spag9 sperm associated antigen 9 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18574703 1322668 Spag9 sperm associated antigen 9 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18574703 1322668 Spag9 sperm associated antigen 9 gene MP:0009280 decreased activated sperm motility IEA N RGD:5509061 20111116 MGI 1322674 Nlrx1 NLR family member X1 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1322674 Nlrx1 NLR family member X1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21703540 1322674 Nlrx1 NLR family member X1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1322674 Nlrx1 NLR family member X1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:21703540 1322674 Nlrx1 NLR family member X1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:21703540 1322674 Nlrx1 NLR family member X1 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:21703540 1322674 Nlrx1 NLR family member X1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21703540 1322674 Nlrx1 NLR family member X1 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:21703540 1322674 Nlrx1 NLR family member X1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21703540 1322674 Nlrx1 NLR family member X1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:21703540 1322674 Nlrx1 NLR family member X1 gene MP:0009084 blind uterus IEA N RGD:5509061 20210520 MGI 1322674 Nlrx1 NLR family member X1 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:21703540 1322677 Dmap1 DNA methyltransferase 1-associated protein 1 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:21383065 1322677 Dmap1 DNA methyltransferase 1-associated protein 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21383065 1322677 Dmap1 DNA methyltransferase 1-associated protein 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21383065 1322677 Dmap1 DNA methyltransferase 1-associated protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322677 Dmap1 DNA methyltransferase 1-associated protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1322677 Dmap1 DNA methyltransferase 1-associated protein 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1322679 Camta2 calmodulin binding transcription activator 2 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:16678093 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15189737 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20201015 MGI PMID:32658897 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15189737 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15189737 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:32658897 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15189737 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15189737 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15189737 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20160630 MGI PMID:26116663 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15189737 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0004264 abnormal extraembryonic tissue physiology IAGP N RGD:5509061 20160630 MGI PMID:26116663 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:15189737 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:15189737 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15189737 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20160630 MGI PMID:26116663 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15189737 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15189737 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160630 MGI PMID:26116663 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20201015 MGI PMID:32658897 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20160630 MGI PMID:26116663 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0011394 increased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20230817 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0031594 increased cardiac jelly amount IAGP N RGD:5509061 20240229 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0031612 increased fetal cardiomyocyte number IAGP N RGD:5509061 20240321 MGI PMID:37254794 1322685 Chd4 chromodomain helicase DNA binding protein 4 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:37254794 1322686 Ift122 intraflagellar transport 122 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:15755804 1322686 Ift122 intraflagellar transport 122 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15755804 1322686 Ift122 intraflagellar transport 122 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21209331 1322686 Ift122 intraflagellar transport 122 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21209331 1322686 Ift122 intraflagellar transport 122 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15755804 1322686 Ift122 intraflagellar transport 122 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1322686 Ift122 intraflagellar transport 122 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:21209331 1322686 Ift122 intraflagellar transport 122 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:21209331 1322686 Ift122 intraflagellar transport 122 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21209331 1322686 Ift122 intraflagellar transport 122 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:14614141 1322686 Ift122 intraflagellar transport 122 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0004131 abnormal motile primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:21209331 1322686 Ift122 intraflagellar transport 122 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:21209331 1322686 Ift122 intraflagellar transport 122 gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:21209331 1322686 Ift122 intraflagellar transport 122 gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0005230 ectrodactyly IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:14614141 1322686 Ift122 intraflagellar transport 122 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:14614141 1322686 Ift122 intraflagellar transport 122 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:21209331 1322686 Ift122 intraflagellar transport 122 gene MP:0010395 abnormal pharyngeal arch development IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 1322686 Ift122 intraflagellar transport 122 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21209331 1322686 Ift122 intraflagellar transport 122 gene MP:0011998 decreased embryonic cilium length IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0012531 delayed limb development IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0012720 elongated neck IAGP N RGD:5509061 20141003 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:21209331 1322686 Ift122 intraflagellar transport 122 gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:19000668 1322686 Ift122 intraflagellar transport 122 gene MP:0030312 enlarged pharyngeal arch IAGP N RGD:5509061 20171109 MGI PMID:21209331 1322693 Pxdc1 PX domain containing 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20221215 MGI 1322695 Fryl FRY like transcription coactivator gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20181227 MGI 1322695 Fryl FRY like transcription coactivator gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322695 Fryl FRY like transcription coactivator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0002083 premature death IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0002095 abnormal skin pigmentation IEA N RGD:5509061 20160804 MGI 1322695 Fryl FRY like transcription coactivator gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0003675 kidney cyst IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0004259 small placenta IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322695 Fryl FRY like transcription coactivator gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0004969 pale kidney IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1322695 Fryl FRY like transcription coactivator gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322695 Fryl FRY like transcription coactivator gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322695 Fryl FRY like transcription coactivator gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20180531 MGI PMID:29409347 1322695 Fryl FRY like transcription coactivator gene MP:0013247 placenta necrosis IAGP N RGD:5509061 20190912 MGI PMID:29539633 1322695 Fryl FRY like transcription coactivator gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:29539633 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0000745 tremors IEA N RGD:5509061 20190502 MGI 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201015 MGI PMID:32017711 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20201015 MGI PMID:27477272 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0002083 premature death IAGP N RGD:5509061 20201015 MGI PMID:32017711 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201015 MGI PMID:27477272 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20201015 MGI PMID:27477272 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20201015 MGI PMID:27477272 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20201015 MGI PMID:32017711 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20201015 MGI PMID:32017711 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20201015 MGI PMID:27477272 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20201015 MGI PMID:32017711 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20201015 MGI PMID:32017711 1322696 Smdt1 single-pass membrane protein with aspartate rich tail 1 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20201015 MGI PMID:32017711 1322700 Osbpl2 oxysterol binding protein-like 2 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20220908 MGI PMID:35041619 1322700 Osbpl2 oxysterol binding protein-like 2 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20220908 MGI PMID:35041619 1322700 Osbpl2 oxysterol binding protein-like 2 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20220908 MGI PMID:35041619 1322700 Osbpl2 oxysterol binding protein-like 2 gene MP:0004300 abnormal organ of Corti supporting cell morphology IAGP N RGD:5509061 20220908 MGI PMID:35041619 1322700 Osbpl2 oxysterol binding protein-like 2 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20220908 MGI PMID:35041619 1322700 Osbpl2 oxysterol binding protein-like 2 gene MP:0006288 small otic capsule IAGP N RGD:5509061 20220908 MGI PMID:35041619 1322700 Osbpl2 oxysterol binding protein-like 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20220908 MGI PMID:35041619 1322700 Osbpl2 oxysterol binding protein-like 2 gene MP:0011061 abnormal inner hair cell kinocilium morphology IAGP N RGD:5509061 20220908 MGI PMID:35041619 1322700 Osbpl2 oxysterol binding protein-like 2 gene MP:0011062 abnormal outer hair cell kinocilium morphology IAGP N RGD:5509061 20220908 MGI PMID:35041619 1322700 Osbpl2 oxysterol binding protein-like 2 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20220908 MGI PMID:35041619 1322700 Osbpl2 oxysterol binding protein-like 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20220908 MGI PMID:35041619 1322700 Osbpl2 oxysterol binding protein-like 2 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20220908 MGI PMID:35041619 1322700 Osbpl2 oxysterol binding protein-like 2 gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:35041619 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20190502 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20190502 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:12024029 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:12024029 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20210520 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12024029 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0001725 abnormal umbilical cord morphology IEA N RGD:5509061 20190502 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20190502 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0002626 increased heart rate IEA N RGD:5509061 20210128 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20230601 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20210520 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20190502 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20210128 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12024029 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1322702 Mthfd2 methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1322705 Frzb frizzled-related protein gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18050203 1322705 Frzb frizzled-related protein gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18050203 1322705 Frzb frizzled-related protein gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:18050203 1322705 Frzb frizzled-related protein gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:22491945 1322705 Frzb frizzled-related protein gene MP:0001405 impaired coordination IEA N RGD:5509061 20111116 MGI 1322705 Frzb frizzled-related protein gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:18050203 1322705 Frzb frizzled-related protein gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 1322705 Frzb frizzled-related protein gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1322705 Frzb frizzled-related protein gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:18050203 1322705 Frzb frizzled-related protein gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:18050203 1322705 Frzb frizzled-related protein gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:18050203 1322705 Frzb frizzled-related protein gene MP:0004149 increased bone strength IAGP N RGD:5509061 20141003 MGI PMID:18050203 1322705 Frzb frizzled-related protein gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:22491945 1322705 Frzb frizzled-related protein gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18050203 1322705 Frzb frizzled-related protein gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:18050203 1322705 Frzb frizzled-related protein gene MP:0014413 decreased depression-related behavior IEA N RGD:5509061 20240425 MGI 1322712 Ythdf2 YTH N6-methyladenosine RNA binding protein 2 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20210128 MGI PMID:32943573 1322712 Ythdf2 YTH N6-methyladenosine RNA binding protein 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210128 MGI PMID:32943573 1322712 Ythdf2 YTH N6-methyladenosine RNA binding protein 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20171102 MGI PMID:28867294 1322712 Ythdf2 YTH N6-methyladenosine RNA binding protein 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20210128 MGI PMID:32943573 1322712 Ythdf2 YTH N6-methyladenosine RNA binding protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20171102 MGI PMID:28867294 1322712 Ythdf2 YTH N6-methyladenosine RNA binding protein 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210128 MGI PMID:32943573 1322712 Ythdf2 YTH N6-methyladenosine RNA binding protein 2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20210128 MGI PMID:32943573 1322712 Ythdf2 YTH N6-methyladenosine RNA binding protein 2 gene MP:0003718 maternal effect IAGP N RGD:5509061 20171102 MGI PMID:28867294 1322712 Ythdf2 YTH N6-methyladenosine RNA binding protein 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20210128 MGI PMID:32943573 1322712 Ythdf2 YTH N6-methyladenosine RNA binding protein 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20210128 MGI PMID:32943573 1322712 Ythdf2 YTH N6-methyladenosine RNA binding protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20171102 MGI PMID:28867294 1322712 Ythdf2 YTH N6-methyladenosine RNA binding protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210128 MGI PMID:32943573 1322715 Nckipsd NCK interacting protein with SH3 domain gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19778379 1322715 Nckipsd NCK interacting protein with SH3 domain gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19302483 1322715 Nckipsd NCK interacting protein with SH3 domain gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:19778379 1322715 Nckipsd NCK interacting protein with SH3 domain gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:19778379 1322715 Nckipsd NCK interacting protein with SH3 domain gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20190704 MGI PMID:19302483 1322720 Acyp1 acylphosphatase 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220519 MGI 1322720 Acyp1 acylphosphatase 1 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20220811 MGI 1322722 Nt5c2 5'-nucleotidase, cytosolic II gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20201022 MGI 1322722 Nt5c2 5'-nucleotidase, cytosolic II gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20201022 MGI 1322722 Nt5c2 5'-nucleotidase, cytosolic II gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1322722 Nt5c2 5'-nucleotidase, cytosolic II gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20191114 MGI PMID:28325731 1322722 Nt5c2 5'-nucleotidase, cytosolic II gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20180405 MGI PMID:29342136 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20201231 MGI 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20200402 MGI 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0006065 abnormal heart position or orientation IEA N RGD:5509061 20210128 MGI 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0008172 abnormal follicular B cell morphology IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0008206 increased B-2 B cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20200213 MGI PMID:31086255 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160421 MGI 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20210826 MGI PMID:30282802 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322724 Otub1 OTU domain, ubiquitin aldehyde binding 1 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20211021 MGI 1322726 Mcm10 minichromosome maintenance 10 replication initiation factor gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21693137 1322726 Mcm10 minichromosome maintenance 10 replication initiation factor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:21693137 1322726 Mcm10 minichromosome maintenance 10 replication initiation factor gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:21693137 1322726 Mcm10 minichromosome maintenance 10 replication initiation factor gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1322726 Mcm10 minichromosome maintenance 10 replication initiation factor gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:21693137 1322726 Mcm10 minichromosome maintenance 10 replication initiation factor gene MP:0004963 abnormal blastocoele morphology IAGP N RGD:5509061 20141003 MGI PMID:21693137 1322726 Mcm10 minichromosome maintenance 10 replication initiation factor gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21693137 1322726 Mcm10 minichromosome maintenance 10 replication initiation factor gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21693137 1322726 Mcm10 minichromosome maintenance 10 replication initiation factor gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:21693137 1322730 Taf5 TATA-box binding protein associated factor 5 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20240919 MGI 1322730 Taf5 TATA-box binding protein associated factor 5 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20240606 MGI PMID:38593904 1322730 Taf5 TATA-box binding protein associated factor 5 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20240606 MGI PMID:38593904 1322730 Taf5 TATA-box binding protein associated factor 5 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20240606 MGI PMID:38593904 1322730 Taf5 TATA-box binding protein associated factor 5 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20240801 MGI PMID:38593904 1322730 Taf5 TATA-box binding protein associated factor 5 gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20240801 MGI PMID:38593904 1322730 Taf5 TATA-box binding protein associated factor 5 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20240801 MGI PMID:38593904 1322730 Taf5 TATA-box binding protein associated factor 5 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20240606 MGI PMID:38593904 1322730 Taf5 TATA-box binding protein associated factor 5 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1322730 Taf5 TATA-box binding protein associated factor 5 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220519 MGI 1322730 Taf5 TATA-box binding protein associated factor 5 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20240606 MGI PMID:38593904 1322730 Taf5 TATA-box binding protein associated factor 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322730 Taf5 TATA-box binding protein associated factor 5 gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20240801 MGI PMID:38593904 1322732 Lta4h leukotriene A4 hydrolase gene MP:0001257 increased body length IEA N RGD:5509061 20210520 MGI 1322732 Lta4h leukotriene A4 hydrolase gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:10586081 1322732 Lta4h leukotriene A4 hydrolase gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10586081 1322733 Wdr81 WD repeat domain 81 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1322733 Wdr81 WD repeat domain 81 gene MP:0000745 tremors IAGP N RGD:5509061 20160609 MGI PMID:12955145 1322733 Wdr81 WD repeat domain 81 gene MP:0000745 tremors IAGP N RGD:5509061 20160630 MGI PMID:23595742 1322733 Wdr81 WD repeat domain 81 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20160630 MGI PMID:23595742 1322733 Wdr81 WD repeat domain 81 gene MP:0001262 decreased body weight IEA N RGD:5509061 20190110 MGI 1322733 Wdr81 WD repeat domain 81 gene MP:0001263 weight loss IAGP N RGD:5509061 20160630 MGI PMID:23595742 1322733 Wdr81 WD repeat domain 81 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20160630 MGI PMID:23595742 1322733 Wdr81 WD repeat domain 81 gene MP:0001393 ataxia IAGP N RGD:5509061 20160630 MGI PMID:23595742 1322733 Wdr81 WD repeat domain 81 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160630 MGI PMID:23595742 1322733 Wdr81 WD repeat domain 81 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160630 MGI PMID:23595742 1322733 Wdr81 WD repeat domain 81 gene MP:0001407 short stride length IAGP N RGD:5509061 20160630 MGI PMID:23595742 1322733 Wdr81 WD repeat domain 81 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1322733 Wdr81 WD repeat domain 81 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1322733 Wdr81 WD repeat domain 81 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20230601 MGI 1322733 Wdr81 WD repeat domain 81 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20160630 MGI PMID:23595742 1322733 Wdr81 WD repeat domain 81 gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20160630 MGI PMID:23595742 1322733 Wdr81 WD repeat domain 81 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210520 MGI 1322733 Wdr81 WD repeat domain 81 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322733 Wdr81 WD repeat domain 81 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20160630 MGI PMID:23595742 1322733 Wdr81 WD repeat domain 81 gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20160630 MGI PMID:23595742 1322733 Wdr81 WD repeat domain 81 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20160630 MGI PMID:23595742 1322733 Wdr81 WD repeat domain 81 gene MP:0014345 abnormal neuron mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:23595742 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0000746 weakness IAGP N RGD:5509061 20150611 MGI PMID:18343091 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:12368912 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:12368912 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0000921 demyelination IAGP N RGD:5509061 20180607 MGI PMID:27485015 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0000958 peripheral nervous system degeneration IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20160407 MGI PMID:25116249 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001393 ataxia IAGP N RGD:5509061 20150611 MGI PMID:18343091 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12368912 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160407 MGI PMID:25116249 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180607 MGI PMID:27485015 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:12368912 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001506 limp posture IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:12368912 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:12368912 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:12368912 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20111116 MGI 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25116249 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12368912 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0003063 increased coping response IEA N RGD:5509061 20111116 MGI 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0003225 axonal dystrophy IEA N RGD:5509061 20111116 MGI 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:12368912 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0004262 abnormal physical strength IEA N RGD:5509061 20111116 MGI 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:12368912 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0004487 type I spiral ligament fibrocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0004489 type III spiral ligament fibrocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20180607 MGI PMID:27485015 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:12368912 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:12368912 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0008532 decreased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:22423107 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:12368912 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:12368912 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0009434 paraparesis IAGP N RGD:5509061 20150611 MGI PMID:18343091 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0012712 spinal cord degeneration IAGP N RGD:5509061 20141003 MGI PMID:14532115 1322735 Slc12a6 solute carrier family 12, member 6 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22423107 1322739 Pigc phosphatidylinositol glycan anchor biosynthesis, class C gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1322739 Pigc phosphatidylinositol glycan anchor biosynthesis, class C gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1322739 Pigc phosphatidylinositol glycan anchor biosynthesis, class C gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1322739 Pigc phosphatidylinositol glycan anchor biosynthesis, class C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322739 Pigc phosphatidylinositol glycan anchor biosynthesis, class C gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1322743 Kpna3 karyopherin subunit alpha 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151224 MGI PMID:21479251 1322743 Kpna3 karyopherin subunit alpha 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20221110 MGI PMID:33058343 1322743 Kpna3 karyopherin subunit alpha 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20221110 MGI PMID:33058343 1322747 Cdc26 cell division cycle 26 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20211021 MGI 1322747 Cdc26 cell division cycle 26 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322748 4930524B15Rik RIKEN cDNA 4930524B15 gene gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1322748 4930524B15Rik RIKEN cDNA 4930524B15 gene gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 1322748 4930524B15Rik RIKEN cDNA 4930524B15 gene gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20210128 MGI 1322750 Dzank1 double zinc ribbon and ankyrin repeat domains 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220519 MGI 1322750 Dzank1 double zinc ribbon and ankyrin repeat domains 1 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 1322750 Dzank1 double zinc ribbon and ankyrin repeat domains 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20171116 MGI PMID:27310661 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20230601 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0000914 exencephaly IEA N RGD:5509061 20230601 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220811 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0001148 enlarged testis IEA N RGD:5509061 20220811 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0001297 microphthalmia IEA N RGD:5509061 20141003 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20230601 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0001785 edema IEA N RGD:5509061 20230601 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0003109 short femur IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0005262 coloboma IEA N RGD:5509061 20141003 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0006290 proboscis IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0008533 abnormal anterior visceral endoderm morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0008797 facial cleft IEA N RGD:5509061 20230601 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0008926 abnormal anterior definitive endoderm morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0010126 abnormal distal visceral endoderm morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0011495 abnormal head shape IEA N RGD:5509061 20230601 MGI 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0012090 midbrain hypoplasia IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322754 Pign phosphatidylinositol glycan anchor biosynthesis, class N gene MP:0030464 abnormal cranial cartilage morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1322756 Pipox pipecolic acid oxidase gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20201022 MGI 1322756 Pipox pipecolic acid oxidase gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20211021 MGI 1322761 Prune2 prune homolog 2 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20200310 MGI PMID:29571668 1322765 Trim47 tripartite motif-containing 47 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220519 MGI 1322767 Mboat1 membrane bound O-acyltransferase domain containing 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210520 MGI 1322767 Mboat1 membrane bound O-acyltransferase domain containing 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 1322770 Phpt1 phosphohistidine phosphatase 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200409 MGI PMID:29440278 1322770 Phpt1 phosphohistidine phosphatase 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200409 MGI PMID:29440278 1322770 Phpt1 phosphohistidine phosphatase 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20200409 MGI PMID:29440278 1322770 Phpt1 phosphohistidine phosphatase 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200409 MGI PMID:29440278 1322770 Phpt1 phosphohistidine phosphatase 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200409 MGI PMID:29440278 1322770 Phpt1 phosphohistidine phosphatase 1 gene MP:0005573 increased pulmonary respiratory rate IEA N RGD:5509061 20201022 MGI 1322770 Phpt1 phosphohistidine phosphatase 1 gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 1322772 Coq8b coenzyme Q8B gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1322772 Coq8b coenzyme Q8B gene MP:0001505 hunched posture IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0002083 premature death IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0002965 increased circulating serum albumin level IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0002989 small kidney IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0003606 kidney failure IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0004969 pale kidney IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1322772 Coq8b coenzyme Q8B gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1322772 Coq8b coenzyme Q8B gene MP:0008062 abnormal podocyte slit junction morphology IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1322772 Coq8b coenzyme Q8B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322772 Coq8b coenzyme Q8B gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20201002 MGI PMID:32381600 1322772 Coq8b coenzyme Q8B gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1322772 Coq8b coenzyme Q8B gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1322772 Coq8b coenzyme Q8B gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1322777 Slc35a1 solute carrier family 35 (CMP-sialic acid transporter), member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1322782 Ptpn3 protein tyrosine phosphatase, non-receptor type 3 gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:17921143 1322782 Ptpn3 protein tyrosine phosphatase, non-receptor type 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17339465 1322782 Ptpn3 protein tyrosine phosphatase, non-receptor type 3 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:17921143 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:18794329 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20141003 MGI 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:18794329 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:18794329 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:18794329 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:18794329 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18794329 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15755804 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:18794329 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0002833 increased heart weight IEA N RGD:5509061 20160804 MGI 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20141003 MGI 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20141003 MGI 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18794329 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:18794329 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:18794329 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0006206 embryonic lethality between somite formation and embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:18794329 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:17507402 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0012183 decreased paraxial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:15755804 1322787 Epb41l5 erythrocyte membrane protein band 4.1 like 5 gene MP:0012272 decreased axial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:15755804 1322791 Tcea3 transcription elongation factor A (SII), 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:22491241 1322793 Eif4g3 eukaryotic translation initiation factor 4 gamma, 3 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20430745 1322793 Eif4g3 eukaryotic translation initiation factor 4 gamma, 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210520 MGI PMID:31999954 1322793 Eif4g3 eukaryotic translation initiation factor 4 gamma, 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:20430745 1322793 Eif4g3 eukaryotic translation initiation factor 4 gamma, 3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:20430745 1322793 Eif4g3 eukaryotic translation initiation factor 4 gamma, 3 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:20430745 1322793 Eif4g3 eukaryotic translation initiation factor 4 gamma, 3 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20190117 MGI PMID:29161344 1322793 Eif4g3 eukaryotic translation initiation factor 4 gamma, 3 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:20430745 1322795 Crlf1 cytokine receptor-like factor 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:14523086 1322795 Crlf1 cytokine receptor-like factor 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:10359701 1322795 Crlf1 cytokine receptor-like factor 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10359701 1322795 Crlf1 cytokine receptor-like factor 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:10359701 1322795 Crlf1 cytokine receptor-like factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10359701 1322797 Pex16 peroxisomal biogenesis factor 16 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20210422 MGI PMID:30511960 1322797 Pex16 peroxisomal biogenesis factor 16 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20210422 MGI PMID:30511960 1322797 Pex16 peroxisomal biogenesis factor 16 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210422 MGI PMID:30511960 1322797 Pex16 peroxisomal biogenesis factor 16 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20210422 MGI PMID:30511960 1322797 Pex16 peroxisomal biogenesis factor 16 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20210422 MGI PMID:30511960 1322797 Pex16 peroxisomal biogenesis factor 16 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20210422 MGI PMID:30511960 1322797 Pex16 peroxisomal biogenesis factor 16 gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20210422 MGI PMID:30511960 1322797 Pex16 peroxisomal biogenesis factor 16 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20210422 MGI PMID:30511960 1322797 Pex16 peroxisomal biogenesis factor 16 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210422 MGI PMID:30511960 1322797 Pex16 peroxisomal biogenesis factor 16 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20210422 MGI PMID:30511960 1322797 Pex16 peroxisomal biogenesis factor 16 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20210422 MGI PMID:30511960 1322797 Pex16 peroxisomal biogenesis factor 16 gene MP:0014396 decreased fat cell mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:30511960 1322797 Pex16 peroxisomal biogenesis factor 16 gene MP:0020520 whitened brown adipose tissue morphology IAGP N RGD:5509061 20210422 MGI PMID:30511960 1322800 Itgb8 integrin beta 8 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0000264 failure of vascular branching IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16251442 1322800 Itgb8 integrin beta 8 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16251442 1322800 Itgb8 integrin beta 8 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16251442 1322800 Itgb8 integrin beta 8 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16251442 1322800 Itgb8 integrin beta 8 gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0003044 impaired basement membrane formation IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1322800 Itgb8 integrin beta 8 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18343643 1322800 Itgb8 integrin beta 8 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16251442 1322800 Itgb8 integrin beta 8 gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322800 Itgb8 integrin beta 8 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20200514 MGI 1322800 Itgb8 integrin beta 8 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:18343643 1322800 Itgb8 integrin beta 8 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:12050137 1322800 Itgb8 integrin beta 8 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:21655088 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:22581779 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:21655088 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:22581779 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:22581779 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22581779 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22581779 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:22581779 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21655088 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:22581779 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21655088 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22581779 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:21655088 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:21655088 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:21655088 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:21655088 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:22581779 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:21655088 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21655088 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22581779 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:22581779 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:21655088 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0004338 small clavicle IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0004831 long incisors IAGP N RGD:5509061 20170928 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:17572665 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:22581779 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:21655088 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:21655088 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:21655088 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322802 Fig4 FIG4 phosphoinositide 5-phosphatase gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:23623387 1322804 Mmp19 matrix metallopeptidase 19 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18523579 1322804 Mmp19 matrix metallopeptidase 19 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18523579 1322804 Mmp19 matrix metallopeptidase 19 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18523579 1322804 Mmp19 matrix metallopeptidase 19 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15169894 1322804 Mmp19 matrix metallopeptidase 19 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18523579 1322804 Mmp19 matrix metallopeptidase 19 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18523579 1322804 Mmp19 matrix metallopeptidase 19 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15169894 1322804 Mmp19 matrix metallopeptidase 19 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18523579 1322804 Mmp19 matrix metallopeptidase 19 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15169894 1322804 Mmp19 matrix metallopeptidase 19 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:15169894 1322804 Mmp19 matrix metallopeptidase 19 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18523579 1322804 Mmp19 matrix metallopeptidase 19 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18523579 1322804 Mmp19 matrix metallopeptidase 19 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18523579 1322804 Mmp19 matrix metallopeptidase 19 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15169894 1322806 Rpia ribose 5-phosphate isomerase A gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1322806 Rpia ribose 5-phosphate isomerase A gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20170105 MGI 1322806 Rpia ribose 5-phosphate isomerase A gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20201022 MGI 1322806 Rpia ribose 5-phosphate isomerase A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322808 Fam210b family with sequence similarity 210, member B gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230601 MGI 1322808 Fam210b family with sequence similarity 210, member B gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20230601 MGI 1322808 Fam210b family with sequence similarity 210, member B gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20240808 MGI PMID:39000360 1322808 Fam210b family with sequence similarity 210, member B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20240808 MGI PMID:39000360 1322808 Fam210b family with sequence similarity 210, member B gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20240808 MGI PMID:39000360 1322808 Fam210b family with sequence similarity 210, member B gene MP:0001212 skin lesions IAGP N RGD:5509061 20240808 MGI PMID:39000360 1322808 Fam210b family with sequence similarity 210, member B gene MP:0002493 increased IgG level IAGP N RGD:5509061 20240808 MGI PMID:39000360 1322808 Fam210b family with sequence similarity 210, member B gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20240808 MGI PMID:39000360 1322808 Fam210b family with sequence similarity 210, member B gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1322808 Fam210b family with sequence similarity 210, member B gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20240808 MGI PMID:39000360 1322808 Fam210b family with sequence similarity 210, member B gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20240808 MGI PMID:39000360 1322808 Fam210b family with sequence similarity 210, member B gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20221215 MGI 1322808 Fam210b family with sequence similarity 210, member B gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20240808 MGI PMID:39000360 1322808 Fam210b family with sequence similarity 210, member B gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20240808 MGI PMID:39000360 1322809 Insc INSC spindle orientation adaptor protein gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:22017987 1322809 Insc INSC spindle orientation adaptor protein gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22017987 1322809 Insc INSC spindle orientation adaptor protein gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22017987 1322809 Insc INSC spindle orientation adaptor protein gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:22017987 1322809 Insc INSC spindle orientation adaptor protein gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20151217 MGI PMID:24135232 1322809 Insc INSC spindle orientation adaptor protein gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22017987 1322809 Insc INSC spindle orientation adaptor protein gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:22017987 1322809 Insc INSC spindle orientation adaptor protein gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20151217 MGI PMID:24135232 1322809 Insc INSC spindle orientation adaptor protein gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:22017987 1322809 Insc INSC spindle orientation adaptor protein gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22017987 1322809 Insc INSC spindle orientation adaptor protein gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20141003 MGI PMID:22017987 1322809 Insc INSC spindle orientation adaptor protein gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20141003 MGI PMID:22017987 1322809 Insc INSC spindle orientation adaptor protein gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:22017987 1322809 Insc INSC spindle orientation adaptor protein gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22017987 1322811 Fanca Fanconi anemia, complementation group A gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:10915769 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:10915769 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:10915769 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:10915769 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:10915769 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10915769 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20151112 MGI PMID:25917546 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10915769 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10915769 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10915769 1322811 Fanca Fanconi anemia, complementation group A gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:10915769 1322811 Fanca Fanconi anemia, complementation group A gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:10915769 1322811 Fanca Fanconi anemia, complementation group A gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:16859999 1322811 Fanca Fanconi anemia, complementation group A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:15905196 1322811 Fanca Fanconi anemia, complementation group A gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:10915769 1322811 Fanca Fanconi anemia, complementation group A gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:10915769 1322811 Fanca Fanconi anemia, complementation group A gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0005158 ovary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20150122 MGI PMID:22922648 1322811 Fanca Fanconi anemia, complementation group A gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20150122 MGI PMID:22922648 1322811 Fanca Fanconi anemia, complementation group A gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:12913077 1322811 Fanca Fanconi anemia, complementation group A gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:12913077 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0000161 scoliosis IEA N RGD:5509061 20220519 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20220811 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20220811 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0000322 increased granulocyte number IEA N RGD:5509061 20211021 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20220519 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0000458 abnormal mandible morphology IEA N RGD:5509061 20220519 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0000552 abnormal radius morphology IEA N RGD:5509061 20220519 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0001255 decreased body height IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0001262 decreased body weight IEA N RGD:5509061 20210128 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0001265 decreased body size IAGP N RGD:5509061 20161103 MGI PMID:22527485 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0001265 decreased body size IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20220811 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0001523 impaired righting response IEA N RGD:5509061 20200514 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20210826 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0002187 abnormal fibula morphology IEA N RGD:5509061 20220519 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0002764 short tibia IEA N RGD:5509061 20221215 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0003109 short femur IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210826 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20220519 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20161103 MGI PMID:22527485 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0004343 small scapula IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0004351 short humerus IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0004507 abnormal ischium morphology IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20220519 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0004672 short ribs IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0004689 small ischium IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20220811 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0005108 abnormal ulna morphology IEA N RGD:5509061 20220519 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0005352 small cranium IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220519 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0005505 thrombocytosis IEA N RGD:5509061 20220811 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20220519 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0008160 increased diameter of humerus IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0009455 enhanced cued conditioning behavior IEA N RGD:5509061 20210520 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0009728 abnormal calcaneum morphology IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20210520 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0010870 absent bone trabeculae IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20161110 MGI PMID:22527485 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20161110 MGI PMID:26803617 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0013675 decreased Ly6C-positive mature NK cell number IEA N RGD:5509061 20210128 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1322813 Tent5a terminal nucleotidyltransferase 5A gene MP:0030279 thin neurocranium IAGP N RGD:5509061 20171102 MGI PMID:26803617 1322815 Kirrel3 kirre like nephrin family adhesion molecule 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201022 MGI PMID:27430022 1322815 Kirrel3 kirre like nephrin family adhesion molecule 3 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:23637329 1322815 Kirrel3 kirre like nephrin family adhesion molecule 3 gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:23637329 1322815 Kirrel3 kirre like nephrin family adhesion molecule 3 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20190425 MGI PMID:28815295 1322815 Kirrel3 kirre like nephrin family adhesion molecule 3 gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23637329 1322815 Kirrel3 kirre like nephrin family adhesion molecule 3 gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20190425 MGI PMID:28815295 1322815 Kirrel3 kirre like nephrin family adhesion molecule 3 gene MP:0011679 abnormal vomeronasal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23637329 1322815 Kirrel3 kirre like nephrin family adhesion molecule 3 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20190425 MGI PMID:28815295 1322815 Kirrel3 kirre like nephrin family adhesion molecule 3 gene MP:0020360 abnormal asymmetric synapse morphology IAGP N RGD:5509061 20190425 MGI PMID:28815295 1322821 Foxp4 forkhead box P4 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15361625 1322821 Foxp4 forkhead box P4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22542185 1322821 Foxp4 forkhead box P4 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22542185 1322821 Foxp4 forkhead box P4 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15361625 1322821 Foxp4 forkhead box P4 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22675208 1322821 Foxp4 forkhead box P4 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:22675208 1322821 Foxp4 forkhead box P4 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22542185 1322821 Foxp4 forkhead box P4 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:22542185 1322821 Foxp4 forkhead box P4 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:22542185 1322821 Foxp4 forkhead box P4 gene MP:0003115 abnormal respiratory system development IAGP N RGD:5509061 20141003 MGI PMID:22675208 1322821 Foxp4 forkhead box P4 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:15361625 1322821 Foxp4 forkhead box P4 gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:15361625 1322821 Foxp4 forkhead box P4 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:15361625 1322821 Foxp4 forkhead box P4 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:22542185 1322821 Foxp4 forkhead box P4 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22675208 1322821 Foxp4 forkhead box P4 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:15361625 1322821 Foxp4 forkhead box P4 gene MP:0010949 decreased club cell number IAGP N RGD:5509061 20141003 MGI PMID:22675208 1322821 Foxp4 forkhead box P4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22675208 1322821 Foxp4 forkhead box P4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15361625 1322821 Foxp4 forkhead box P4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22542185 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0000358 abnormal cell morphology IEA N RGD:5509061 20111222 MGI 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0001262 decreased body weight IEA N RGD:5509061 20111116 MGI 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20111215 MGI 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20111116 MGI 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0002573 behavioral despair IEA N RGD:5509061 20111116 MGI 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0004267 abnormal optic tract morphology IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20111116 MGI 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0006325 impaired hearing IEA N RGD:5509061 20111116 MGI 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322824 Slc17a5 solute carrier family 17 (anion/sugar transporter), member 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20007460 1322826 Abhd2 abhydrolase domain containing 2 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20230119 MGI PMID:34568325 1322826 Abhd2 abhydrolase domain containing 2 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20230119 MGI PMID:34568325 1322826 Abhd2 abhydrolase domain containing 2 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20230119 MGI PMID:34568325 1322826 Abhd2 abhydrolase domain containing 2 gene MP:0002681 increased corpora lutea number IAGP N RGD:5509061 20230119 MGI PMID:34568325 1322826 Abhd2 abhydrolase domain containing 2 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:15721306 1322826 Abhd2 abhydrolase domain containing 2 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:15721306 1322826 Abhd2 abhydrolase domain containing 2 gene MP:0008870 increased mature ovarian follicle number IAGP N RGD:5509061 20230119 MGI PMID:34568325 1322826 Abhd2 abhydrolase domain containing 2 gene MP:0009012 short diestrus IAGP N RGD:5509061 20230119 MGI PMID:34568325 1322826 Abhd2 abhydrolase domain containing 2 gene MP:0009015 short proestrus IAGP N RGD:5509061 20230119 MGI PMID:34568325 1322826 Abhd2 abhydrolase domain containing 2 gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20230119 MGI PMID:34568325 1322826 Abhd2 abhydrolase domain containing 2 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20230119 MGI PMID:34568325 1322826 Abhd2 abhydrolase domain containing 2 gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20230119 MGI PMID:34568325 1322826 Abhd2 abhydrolase domain containing 2 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20230119 MGI PMID:34568325 1322826 Abhd2 abhydrolase domain containing 2 gene MP:0031421 increased superovulation rate IAGP N RGD:5509061 20230119 MGI PMID:34568325 1322828 Rfxank regulatory factor X-associated ankyrin-containing protein gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1322828 Rfxank regulatory factor X-associated ankyrin-containing protein gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210128 MGI 1322828 Rfxank regulatory factor X-associated ankyrin-containing protein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1322829 Vps53 VPS53 GARP complex subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18511934 1322829 Vps53 VPS53 GARP complex subunit gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:18511934 1322829 Vps53 VPS53 GARP complex subunit gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18511934 1322829 Vps53 VPS53 GARP complex subunit gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20201231 MGI 1322829 Vps53 VPS53 GARP complex subunit gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:18511934 1322829 Vps53 VPS53 GARP complex subunit gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18511934 1322829 Vps53 VPS53 GARP complex subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322832 Lman2l lectin, mannose-binding 2-like gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1322832 Lman2l lectin, mannose-binding 2-like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1322835 Pgap6 post-glycosylphosphatidylinositol attachment to proteins 6 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1322835 Pgap6 post-glycosylphosphatidylinositol attachment to proteins 6 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1322835 Pgap6 post-glycosylphosphatidylinositol attachment to proteins 6 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20180628 MGI PMID:27881714 1322835 Pgap6 post-glycosylphosphatidylinositol attachment to proteins 6 gene MP:0001925 male infertility IEA N RGD:5509061 20230601 MGI 1322835 Pgap6 post-glycosylphosphatidylinositol attachment to proteins 6 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1322835 Pgap6 post-glycosylphosphatidylinositol attachment to proteins 6 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20180628 MGI PMID:27881714 1322835 Pgap6 post-glycosylphosphatidylinositol attachment to proteins 6 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20180628 MGI PMID:27881714 1322835 Pgap6 post-glycosylphosphatidylinositol attachment to proteins 6 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1322839 Slc41a1 solute carrier family 41, member 1 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20240404 MGI PMID:36049064 1322839 Slc41a1 solute carrier family 41, member 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20240314 MGI PMID:33153064 1322839 Slc41a1 solute carrier family 41, member 1 gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20240314 MGI PMID:33153064 1322841 Il17f interleukin 17F gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:19075395 1322841 Il17f interleukin 17F gene MP:0001866 nasal inflammation IAGP N RGD:5509061 20141003 MGI PMID:19144317 1322841 Il17f interleukin 17F gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19119024 1322841 Il17f interleukin 17F gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:19144317 1322841 Il17f interleukin 17F gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22770884 1322841 Il17f interleukin 17F gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:18411338 1322841 Il17f interleukin 17F gene MP:0002742 enlarged submandibular lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19144317 1322841 Il17f interleukin 17F gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20141003 MGI PMID:19144317 1322841 Il17f interleukin 17F gene MP:0003747 mouth mucosal ulcer IAGP N RGD:5509061 20141003 MGI PMID:19144317 1322841 Il17f interleukin 17F gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:18411338 1322841 Il17f interleukin 17F gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:18411338 1322841 Il17f interleukin 17F gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22770884 1322841 Il17f interleukin 17F gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22770884 1322841 Il17f interleukin 17F gene MP:0008348 absent gamma-delta T cells IAGP N RGD:5509061 20141003 MGI PMID:22770884 1322841 Il17f interleukin 17F gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:19144317 1322841 Il17f interleukin 17F gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19144317 1322841 Il17f interleukin 17F gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:18411338 1322841 Il17f interleukin 17F gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:19144317 1322841 Il17f interleukin 17F gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:19144317 1322841 Il17f interleukin 17F gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:18411338 1322841 Il17f interleukin 17F gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:18411338 1322841 Il17f interleukin 17F gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:19075395 1322841 Il17f interleukin 17F gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:22770884 1322841 Il17f interleukin 17F gene MP:0009787 increased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20493731 1322845 Prpf40a pre-mRNA processing factor 40A gene MP:0001304 cataract IEA N RGD:5509061 20210128 MGI 1322845 Prpf40a pre-mRNA processing factor 40A gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 1322845 Prpf40a pre-mRNA processing factor 40A gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1322845 Prpf40a pre-mRNA processing factor 40A gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1322845 Prpf40a pre-mRNA processing factor 40A gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 1322845 Prpf40a pre-mRNA processing factor 40A gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1322845 Prpf40a pre-mRNA processing factor 40A gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1322845 Prpf40a pre-mRNA processing factor 40A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322845 Prpf40a pre-mRNA processing factor 40A gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1322848 Rrs1 ribosome biogenesis regulator 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1322848 Rrs1 ribosome biogenesis regulator 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 1322848 Rrs1 ribosome biogenesis regulator 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322848 Rrs1 ribosome biogenesis regulator 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210520 MGI 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240523 MGI 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0000274 enlarged heart IEA N RGD:5509061 20240523 MGI 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17906629 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:17906629 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:17906629 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17906629 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0004966 abnormal inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:17906629 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17906629 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17906629 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17906629 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17906629 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17906629 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20240523 MGI 1322850 Cops8 COP9 signalosome subunit 8 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20240523 MGI 1322854 Gpr183 G protein-coupled receptor 183 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:19615922 1322854 Gpr183 G protein-coupled receptor 183 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19615922 1322854 Gpr183 G protein-coupled receptor 183 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20210520 MGI 1322854 Gpr183 G protein-coupled receptor 183 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20210520 MGI 1322854 Gpr183 G protein-coupled receptor 183 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19615922 1322854 Gpr183 G protein-coupled receptor 183 gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19615922 1322854 Gpr183 G protein-coupled receptor 183 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:19615922 1322854 Gpr183 G protein-coupled receptor 183 gene MP:0008122 decreased myeloid dendritic cell number IAGP N RGD:5509061 20141009 MGI PMID:24386204 1322854 Gpr183 G protein-coupled receptor 183 gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141009 MGI PMID:24386204 1322854 Gpr183 G protein-coupled receptor 183 gene MP:0008191 abnormal follicular B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19597478 1322854 Gpr183 G protein-coupled receptor 183 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19615922 1322854 Gpr183 G protein-coupled receptor 183 gene MP:0008550 abnormal circulating interferon-beta level IAGP N RGD:5509061 20141009 MGI PMID:24386204 1322854 Gpr183 G protein-coupled receptor 183 gene MP:0008573 increased circulating interferon-alpha level IAGP N RGD:5509061 20141009 MGI PMID:24386204 1322854 Gpr183 G protein-coupled receptor 183 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141009 MGI PMID:24386204 1322854 Gpr183 G protein-coupled receptor 183 gene MP:0014472 impaired B cell migration IAGP N RGD:5509061 20240613 MGI PMID:19615922 1322856 Gprc5c G protein-coupled receptor, family C, group 5, member C gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:21840300 1322856 Gprc5c G protein-coupled receptor, family C, group 5, member C gene MP:0002606 increased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21840300 1322856 Gprc5c G protein-coupled receptor, family C, group 5, member C gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:21840300 1322856 Gprc5c G protein-coupled receptor, family C, group 5, member C gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:21840300 1322856 Gprc5c G protein-coupled receptor, family C, group 5, member C gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:21840300 1322856 Gprc5c G protein-coupled receptor, family C, group 5, member C gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:21840300 1322861 Ppie peptidylprolyl isomerase E (cyclophilin E) gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1322861 Ppie peptidylprolyl isomerase E (cyclophilin E) gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20220811 MGI 1322861 Ppie peptidylprolyl isomerase E (cyclophilin E) gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1322861 Ppie peptidylprolyl isomerase E (cyclophilin E) gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1322861 Ppie peptidylprolyl isomerase E (cyclophilin E) gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220519 MGI 1322861 Ppie peptidylprolyl isomerase E (cyclophilin E) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1322861 Ppie peptidylprolyl isomerase E (cyclophilin E) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1322867 Eef1b2 eukaryotic translation elongation factor 1 beta 2 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20201022 MGI 1322867 Eef1b2 eukaryotic translation elongation factor 1 beta 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20240523 MGI 1322867 Eef1b2 eukaryotic translation elongation factor 1 beta 2 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20210520 MGI 1322867 Eef1b2 eukaryotic translation elongation factor 1 beta 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1322867 Eef1b2 eukaryotic translation elongation factor 1 beta 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20240523 MGI 1322867 Eef1b2 eukaryotic translation elongation factor 1 beta 2 gene MP:0001513 limb grasping IEA N RGD:5509061 20200402 MGI 1322867 Eef1b2 eukaryotic translation elongation factor 1 beta 2 gene MP:0001523 impaired righting response IEA N RGD:5509061 20200402 MGI 1322867 Eef1b2 eukaryotic translation elongation factor 1 beta 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220519 MGI 1322867 Eef1b2 eukaryotic translation elongation factor 1 beta 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1322867 Eef1b2 eukaryotic translation elongation factor 1 beta 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 1322867 Eef1b2 eukaryotic translation elongation factor 1 beta 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20240523 MGI 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:19893033 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:19893033 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:18382769 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:19893033 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:18382769 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:19893033 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:18382769 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:19893033 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:10523500 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:18382769 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:19893033 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0001208 blistering IAGP N RGD:5509061 20200310 MGI PMID:28892093 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18382769 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:18382769 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10523500 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18382769 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19893033 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18382769 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19893033 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:18382769 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18382769 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18382769 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0008041 absent NK T cells IAGP N RGD:5509061 20200310 MGI PMID:28892093 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0008070 absent T cells IAGP N RGD:5509061 20200310 MGI PMID:28892093 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0008071 absent B cells IAGP N RGD:5509061 20200310 MGI PMID:28892093 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18382769 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18382769 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:18382769 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10523500 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19893033 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20141003 MGI PMID:18382769 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20141003 MGI PMID:19893033 1322870 Col7a1 collagen, type VII, alpha 1 gene MP:0030101 carious teeth IAGP N RGD:5509061 20170928 MGI PMID:19893033 1322874 Dmtn dematin actin binding protein gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12011427 1322874 Dmtn dematin actin binding protein gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12011427 1322874 Dmtn dematin actin binding protein gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:12011427 1322874 Dmtn dematin actin binding protein gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:12011427 1322874 Dmtn dematin actin binding protein gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:12011427 1322874 Dmtn dematin actin binding protein gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:12011427 1322874 Dmtn dematin actin binding protein gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:12011427 1322884 Eif2d eukaryotic translation initiation factor 2D gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1322884 Eif2d eukaryotic translation initiation factor 2D gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1322884 Eif2d eukaryotic translation initiation factor 2D gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1322884 Eif2d eukaryotic translation initiation factor 2D gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1322884 Eif2d eukaryotic translation initiation factor 2D gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1322887 Lrba LPS-responsive beige-like anchor gene MP:0000023 abnormal ear position IEA N RGD:5509061 20181227 MGI 1322887 Lrba LPS-responsive beige-like anchor gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 1322887 Lrba LPS-responsive beige-like anchor gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1322887 Lrba LPS-responsive beige-like anchor gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1322887 Lrba LPS-responsive beige-like anchor gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 1322887 Lrba LPS-responsive beige-like anchor gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20161222 MGI PMID:27824136 1322887 Lrba LPS-responsive beige-like anchor gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20161222 MGI PMID:27824136 1322887 Lrba LPS-responsive beige-like anchor gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20161222 MGI PMID:27824136 1322887 Lrba LPS-responsive beige-like anchor gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1322887 Lrba LPS-responsive beige-like anchor gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1322887 Lrba LPS-responsive beige-like anchor gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1322887 Lrba LPS-responsive beige-like anchor gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20181227 MGI 1322887 Lrba LPS-responsive beige-like anchor gene MP:0005673 decreased susceptibility to graft versus host disease IAGP N RGD:5509061 20161222 MGI PMID:27824136 1322887 Lrba LPS-responsive beige-like anchor gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20181227 MGI 1322887 Lrba LPS-responsive beige-like anchor gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20190627 MGI PMID:31097594 1322887 Lrba LPS-responsive beige-like anchor gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20181227 MGI 1322887 Lrba LPS-responsive beige-like anchor gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20161222 MGI PMID:27824136 1322887 Lrba LPS-responsive beige-like anchor gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20161222 MGI PMID:27824136 1322888 Kansl1 KAT8 regulatory NSL complex subunit 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21492964 1322888 Kansl1 KAT8 regulatory NSL complex subunit 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20241107 MGI PMID:35177641 1322888 Kansl1 KAT8 regulatory NSL complex subunit 1 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:21492964 1322888 Kansl1 KAT8 regulatory NSL complex subunit 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20241107 MGI PMID:35177641 1322888 Kansl1 KAT8 regulatory NSL complex subunit 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20241107 MGI PMID:35177641 1322888 Kansl1 KAT8 regulatory NSL complex subunit 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20241107 MGI PMID:35177641 1322888 Kansl1 KAT8 regulatory NSL complex subunit 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20241107 MGI PMID:35177641 1322888 Kansl1 KAT8 regulatory NSL complex subunit 1 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20241107 MGI PMID:35177641 1322888 Kansl1 KAT8 regulatory NSL complex subunit 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20241107 MGI PMID:35177641 1322888 Kansl1 KAT8 regulatory NSL complex subunit 1 gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20241107 MGI PMID:35177641 1322888 Kansl1 KAT8 regulatory NSL complex subunit 1 gene MP:0014345 abnormal neuron mitochondrial morphology IAGP N RGD:5509061 20241107 MGI PMID:35177641 1322888 Kansl1 KAT8 regulatory NSL complex subunit 1 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20241107 MGI PMID:35177641 1322888 Kansl1 KAT8 regulatory NSL complex subunit 1 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20241107 MGI PMID:35177641 1322893 Sipa1l3 signal-induced proliferation-associated 1 like 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20161103 MGI PMID:26231217 1322893 Sipa1l3 signal-induced proliferation-associated 1 like 3 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20161103 MGI PMID:26231217 1322893 Sipa1l3 signal-induced proliferation-associated 1 like 3 gene MP:0001304 cataract IAGP N RGD:5509061 20161103 MGI PMID:26231217 1322893 Sipa1l3 signal-induced proliferation-associated 1 like 3 gene MP:0001306 small lens IAGP N RGD:5509061 20161103 MGI PMID:26231217 1322893 Sipa1l3 signal-induced proliferation-associated 1 like 3 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20161103 MGI PMID:26231217 1322893 Sipa1l3 signal-induced proliferation-associated 1 like 3 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20161103 MGI PMID:26231217 1322893 Sipa1l3 signal-induced proliferation-associated 1 like 3 gene MP:0011482 posterior iris synechia IAGP N RGD:5509061 20161103 MGI PMID:26231217 1322897 Ap1ar adaptor-related protein complex 1 associated regulatory protein gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20190502 MGI 1322897 Ap1ar adaptor-related protein complex 1 associated regulatory protein gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20201022 MGI 1322897 Ap1ar adaptor-related protein complex 1 associated regulatory protein gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1322897 Ap1ar adaptor-related protein complex 1 associated regulatory protein gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1322897 Ap1ar adaptor-related protein complex 1 associated regulatory protein gene MP:0003960 increased lean body mass IEA N RGD:5509061 20190502 MGI 1322897 Ap1ar adaptor-related protein complex 1 associated regulatory protein gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20190502 MGI 1322897 Ap1ar adaptor-related protein complex 1 associated regulatory protein gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1322899 Pfdn5 prefoldin 5 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20190502 MGI 1322899 Pfdn5 prefoldin 5 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1322899 Pfdn5 prefoldin 5 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1322899 Pfdn5 prefoldin 5 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20201231 MGI 1322899 Pfdn5 prefoldin 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20190502 MGI 1322899 Pfdn5 prefoldin 5 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1322899 Pfdn5 prefoldin 5 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1322899 Pfdn5 prefoldin 5 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0009325 necrospermia IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1322899 Pfdn5 prefoldin 5 gene MP:0010236 abnormal retina outer limiting membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:20956523 1322899 Pfdn5 prefoldin 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322899 Pfdn5 prefoldin 5 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1322899 Pfdn5 prefoldin 5 gene MP:0030966 decreased brain ependyma motile cilium number IAGP N RGD:5509061 20190725 MGI PMID:20956523 1322901 Orc6 origin recognition complex, subunit 6 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 1322901 Orc6 origin recognition complex, subunit 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1322901 Orc6 origin recognition complex, subunit 6 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20240926 MGI 1322901 Orc6 origin recognition complex, subunit 6 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20191205 MGI 1322901 Orc6 origin recognition complex, subunit 6 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1322901 Orc6 origin recognition complex, subunit 6 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20181227 MGI 1322901 Orc6 origin recognition complex, subunit 6 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20191205 MGI 1322901 Orc6 origin recognition complex, subunit 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322901 Orc6 origin recognition complex, subunit 6 gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20191205 MGI 1322901 Orc6 origin recognition complex, subunit 6 gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20191205 MGI 1322901 Orc6 origin recognition complex, subunit 6 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1322903 Pigh phosphatidylinositol glycan anchor biosynthesis, class H gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1322903 Pigh phosphatidylinositol glycan anchor biosynthesis, class H gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20231207 MGI 1322903 Pigh phosphatidylinositol glycan anchor biosynthesis, class H gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1322903 Pigh phosphatidylinositol glycan anchor biosynthesis, class H gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322903 Pigh phosphatidylinositol glycan anchor biosynthesis, class H gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1322903 Pigh phosphatidylinositol glycan anchor biosynthesis, class H gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:19060336 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12361974 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:18367557 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:18367557 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12361974 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12361974 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18367557 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:16163358 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:18367557 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:19023080 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:11543617 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19023080 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:12361974 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19060336 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:11543617 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:11543617 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:19060336 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:18367557 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17199045 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:19060336 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0003613 abnormal kidney medulla development IAGP N RGD:5509061 20141003 MGI PMID:19060336 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:18367557 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12361974 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:19060336 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0005167 abnormal blood-brain barrier function IAGP N RGD:5509061 20141003 MGI PMID:19023080 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:18367557 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19023080 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17199045 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:17199045 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:16163358 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0009573 abnormal right lung middle lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:18367557 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0010816 decreased type I pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:12361974 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19060336 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12361974 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18367557 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16163358 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11543617 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18367557 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19023080 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011144 thin lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:12361974 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011144 thin lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:18367557 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011146 abnormal mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:12361974 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011148 decreased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:18367557 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011345 truncated loop of Henle IAGP N RGD:5509061 20141003 MGI PMID:19060336 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19060336 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011438 absent kidney medulla IAGP N RGD:5509061 20141003 MGI PMID:19060336 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011439 abnormal kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19060336 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19060336 1322907 Wnt7b wingless-type MMTV integration site family, member 7B gene MP:0011843 abnormal kidney collecting duct epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19060336 1322909 Arhgap10 Rho GTPase activating protein 10 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210128 MGI 1322909 Arhgap10 Rho GTPase activating protein 10 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1322909 Arhgap10 Rho GTPase activating protein 10 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 1322909 Arhgap10 Rho GTPase activating protein 10 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1322909 Arhgap10 Rho GTPase activating protein 10 gene MP:0001393 ataxia IEA N RGD:5509061 20141003 MGI 1322909 Arhgap10 Rho GTPase activating protein 10 gene MP:0001405 impaired coordination IEA N RGD:5509061 20141003 MGI 1322909 Arhgap10 Rho GTPase activating protein 10 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1322909 Arhgap10 Rho GTPase activating protein 10 gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20141003 MGI 1322909 Arhgap10 Rho GTPase activating protein 10 gene MP:0002566 abnormal sexual interaction IEA N RGD:5509061 20141003 MGI 1322909 Arhgap10 Rho GTPase activating protein 10 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210520 MGI 1322909 Arhgap10 Rho GTPase activating protein 10 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201022 MGI 1322909 Arhgap10 Rho GTPase activating protein 10 gene MP:0009434 paraparesis IEA N RGD:5509061 20141003 MGI 1322911 Rras related RAS viral (r-ras) oncogene gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 1322911 Rras related RAS viral (r-ras) oncogene gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1322911 Rras related RAS viral (r-ras) oncogene gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20210304 MGI PMID:22174156 1322911 Rras related RAS viral (r-ras) oncogene gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20240523 MGI 1322911 Rras related RAS viral (r-ras) oncogene gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:16286923 1322911 Rras related RAS viral (r-ras) oncogene gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20210304 MGI PMID:22174156 1322911 Rras related RAS viral (r-ras) oncogene gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:16286923 1322911 Rras related RAS viral (r-ras) oncogene gene MP:0005017 decreased B cell number IEA N RGD:5509061 20141003 MGI 1322911 Rras related RAS viral (r-ras) oncogene gene MP:0005461 abnormal dendritic cell morphology IAGP N RGD:5509061 20210304 MGI PMID:22174156 1322911 Rras related RAS viral (r-ras) oncogene gene MP:0006135 artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:16286923 1322911 Rras related RAS viral (r-ras) oncogene gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20141003 MGI 1322911 Rras related RAS viral (r-ras) oncogene gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20141003 MGI 1322911 Rras related RAS viral (r-ras) oncogene gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1322911 Rras related RAS viral (r-ras) oncogene gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:16286923 1322911 Rras related RAS viral (r-ras) oncogene gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17923475 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17923475 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230316 MGI PMID:36719796 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0002083 premature death IAGP N RGD:5509061 20230316 MGI PMID:36719796 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20230316 MGI PMID:36719796 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:17923475 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20230316 MGI PMID:36719796 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:17923475 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17923475 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20230316 MGI PMID:36719796 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17923475 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:17923475 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:17923475 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17923475 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:17923475 1322912 Pnpla8 patatin-like phospholipase domain containing 8 gene MP:0030753 decreased choline level IAGP N RGD:5509061 20230316 MGI PMID:36719796 1322914 Snorc secondary ossification center associated regulator of chondrocyte maturation gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20170323 MGI 1322914 Snorc secondary ossification center associated regulator of chondrocyte maturation gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20170323 MGI 1322914 Snorc secondary ossification center associated regulator of chondrocyte maturation gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20170323 MGI 1322920 Nmral1 NmrA-like family domain containing 1 gene MP:0001314 cornea opacity IEA N RGD:5509061 20231207 MGI 1322920 Nmral1 NmrA-like family domain containing 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1322920 Nmral1 NmrA-like family domain containing 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20201210 MGI PMID:31796584 1322920 Nmral1 NmrA-like family domain containing 1 gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 1322920 Nmral1 NmrA-like family domain containing 1 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20201210 MGI PMID:31796584 1322920 Nmral1 NmrA-like family domain containing 1 gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20201210 MGI PMID:31796584 1322920 Nmral1 NmrA-like family domain containing 1 gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20231207 MGI 1322920 Nmral1 NmrA-like family domain containing 1 gene MP:0012125 decreased bronchoconstrictive response IEA N RGD:5509061 20201022 MGI 1322922 Golm1 golgi membrane protein 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322922 Golm1 golgi membrane protein 1 gene MP:0011508 abnormal glomerular capillary thrombosis IAGP N RGD:5509061 20141003 MGI PMID:18830387 1322927 Mindy2 MINDY lysine 48 deubiquitinase 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1322927 Mindy2 MINDY lysine 48 deubiquitinase 2 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20181227 MGI 1322927 Mindy2 MINDY lysine 48 deubiquitinase 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1322927 Mindy2 MINDY lysine 48 deubiquitinase 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230601 MGI 1322927 Mindy2 MINDY lysine 48 deubiquitinase 2 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20181227 MGI 1322931 Nkd2 naked cuticle 2 gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:17438140 1322931 Nkd2 naked cuticle 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17438140 1322931 Nkd2 naked cuticle 2 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:17438140 1322931 Nkd2 naked cuticle 2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:17438140 1322934 Mmrn2 multimerin 2 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20210603 MGI PMID:31422156 1322934 Mmrn2 multimerin 2 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20210603 MGI PMID:31422156 1322934 Mmrn2 multimerin 2 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20210603 MGI PMID:31422156 1322942 Myct1 myc target 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1322942 Myct1 myc target 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1322942 Myct1 myc target 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1322942 Myct1 myc target 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1322942 Myct1 myc target 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1322942 Myct1 myc target 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20210520 MGI PMID:33658356 1322942 Myct1 myc target 1 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20210520 MGI PMID:33658356 1322942 Myct1 myc target 1 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20210520 MGI PMID:33658356 1322942 Myct1 myc target 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1322942 Myct1 myc target 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20210520 MGI PMID:33658356 1322942 Myct1 myc target 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1322942 Myct1 myc target 1 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20210520 MGI PMID:33658356 1322942 Myct1 myc target 1 gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20210520 MGI PMID:33658356 1322942 Myct1 myc target 1 gene MP:0020202 abnormal macrophage cell number IAGP N RGD:5509061 20210520 MGI PMID:33658356 1322948 Prrx2 paired related homeobox 2 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0000023 abnormal ear position IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0000448 pointed snout IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0000486 abnormal pulmonary trunk morphology IAGP N RGD:5509061 20141003 MGI PMID:10664157 1322948 Prrx2 paired related homeobox 2 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0000568 ectopic digits IAGP N RGD:5509061 20141003 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0001341 absent eyelids IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10664157 1322948 Prrx2 paired related homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:10664157 1322948 Prrx2 paired related homeobox 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0003142 anotia IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:10664157 1322948 Prrx2 paired related homeobox 2 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:10664157 1322948 Prrx2 paired related homeobox 2 gene MP:0004347 abnormal scapular spine morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0004479 abnormal oval window morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0004603 absent vertebral arch IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0004679 xiphoid process foramen IAGP N RGD:5509061 20181018 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0004899 absent temporal bone squamous part IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0004900 absent zygomatic arch IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0005359 growth retardation of incisors IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0006288 small otic capsule IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0008919 fused tarsal bones IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20181101 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0009744 postaxial polydactyly IAGP N RGD:5509061 20181101 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0009918 abnormal stylohyoid ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0010464 abnormal aortic arch and aortic arch branch attachment IAGP N RGD:5509061 20141003 MGI PMID:10664157 1322948 Prrx2 paired related homeobox 2 gene MP:0010564 abnormal fetal ductus arteriosus morphology IAGP N RGD:5509061 20141003 MGI PMID:10664157 1322948 Prrx2 paired related homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0020823 absent pubic symphysis IAGP N RGD:5509061 20181018 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0030297 outer ear hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0030317 absent maxillary zygomatic process IAGP N RGD:5509061 20171109 MGI PMID:9729491 1322948 Prrx2 paired related homeobox 2 gene MP:0030317 absent maxillary zygomatic process IAGP N RGD:5509061 20171109 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0030456 abnormal odontoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0030471 abnormal ameloblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:9876178 1322948 Prrx2 paired related homeobox 2 gene MP:0030862 absent triquetrum IAGP N RGD:5509061 20181101 MGI PMID:9882503 1322948 Prrx2 paired related homeobox 2 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:9729491 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:15809037 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:16890158 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:17156747 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0000445 short snout IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:15937482 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:17156747 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:15937482 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:15937482 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15937482 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23150596 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17156747 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17156747 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15809037 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15937482 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:15809037 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:15937482 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15937482 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:17156747 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:17156747 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:15937482 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15809037 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20141003 MGI PMID:16890158 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004300 abnormal organ of Corti supporting cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15809037 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004375 enlarged frontal bone IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004386 enlarged interparietal bone IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004391 abnormal respiratory conducting tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17156747 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15809037 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004430 abnormal Claudius cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15809037 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004444 small supraoccipital bone IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004548 dilated esophagus IAGP N RGD:5509061 20141003 MGI PMID:15937482 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004594 abnormal mandibular coronoid process morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004595 abnormal mandibular condyloid process morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004600 abnormal vertebral transverse process morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004670 small vertebral body IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0004840 increased Deiters cell number IAGP N RGD:5509061 20141003 MGI PMID:15809037 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:17156747 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17369402 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:23150596 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20141003 MGI PMID:17693063 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:17693063 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0010079 increased osteochondroma incidence IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23150596 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17369402 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15809037 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17156747 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17156747 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17156747 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17156747 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0011861 increased cranium height IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:15809037 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15809037 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0014277 alobar holoprosencephaly IAGP N RGD:5509061 20230810 MGI PMID:17156747 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0021170 spinal stenosis IAGP N RGD:5509061 20220721 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0030315 small neurocranium IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0030425 wide intermaxillary suture IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20171221 MGI PMID:16890158 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0030536 abnormal diastema morphology IAGP N RGD:5509061 20180201 MGI PMID:16890158 1322950 Spry2 sprouty RTK signaling antagonist 2 gene MP:0031283 increased enchondroma incidence IAGP N RGD:5509061 20220714 MGI PMID:34423857 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0001261 obese IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0010580 decreased heart left ventricle size IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20180607 MGI PMID:28835921 1322952 Ptcd1 pentatricopeptide repeat domain 1 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:28835921 1322955 Ccdc88b coiled-coil domain containing 88B gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1322955 Ccdc88b coiled-coil domain containing 88B gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20190502 MGI 1322955 Ccdc88b coiled-coil domain containing 88B gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1322955 Ccdc88b coiled-coil domain containing 88B gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20160512 MGI PMID:25403443 1322955 Ccdc88b coiled-coil domain containing 88B gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20160512 MGI PMID:25403443 1322955 Ccdc88b coiled-coil domain containing 88B gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20160512 MGI PMID:25403443 1322955 Ccdc88b coiled-coil domain containing 88B gene MP:0008528 polycystic kidney IEA N RGD:5509061 20190502 MGI 1322955 Ccdc88b coiled-coil domain containing 88B gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20160512 MGI PMID:25403443 1322955 Ccdc88b coiled-coil domain containing 88B gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20160512 MGI PMID:25403443 1322955 Ccdc88b coiled-coil domain containing 88B gene MP:0010751 decreased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20160512 MGI PMID:25403443 1322955 Ccdc88b coiled-coil domain containing 88B gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1322955 Ccdc88b coiled-coil domain containing 88B gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20160512 MGI PMID:25403443 1322958 Sf3a1 splicing factor 3a, subunit 1 gene MP:0006204 embryonic lethality before implantation IEA N RGD:5509061 20111116 MGI 1322963 Xcr1 chemokine (C motif) receptor 1 gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:23670193 1322963 Xcr1 chemokine (C motif) receptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23670193 1322963 Xcr1 chemokine (C motif) receptor 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19913446 1322963 Xcr1 chemokine (C motif) receptor 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23670193 1322963 Xcr1 chemokine (C motif) receptor 1 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23670193 1322963 Xcr1 chemokine (C motif) receptor 1 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23670193 1322963 Xcr1 chemokine (C motif) receptor 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23670193 1322964 Batf2 basic leucine zipper transcription factor, ATF-like 2 gene MP:0001393 ataxia IEA N RGD:5509061 20170209 MGI 1322964 Batf2 basic leucine zipper transcription factor, ATF-like 2 gene MP:0010750 increased susceptibility to parasitic infection induced morbidity/mortality IEA N RGD:5509061 20141003 MGI 1322967 Kpna4 karyopherin subunit alpha 4 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20220811 MGI 1322967 Kpna4 karyopherin subunit alpha 4 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20221110 MGI PMID:33058343 1322967 Kpna4 karyopherin subunit alpha 4 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20201022 MGI 1322967 Kpna4 karyopherin subunit alpha 4 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1322967 Kpna4 karyopherin subunit alpha 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20221110 MGI PMID:33058343 1322967 Kpna4 karyopherin subunit alpha 4 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20221110 MGI PMID:33058343 1322967 Kpna4 karyopherin subunit alpha 4 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20221110 MGI PMID:33058343 1322967 Kpna4 karyopherin subunit alpha 4 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20221110 MGI PMID:33058343 1322967 Kpna4 karyopherin subunit alpha 4 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20221110 MGI PMID:33058343 1322967 Kpna4 karyopherin subunit alpha 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20221110 MGI PMID:33058343 1322967 Kpna4 karyopherin subunit alpha 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20221110 MGI PMID:33058343 1322967 Kpna4 karyopherin subunit alpha 4 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20221110 MGI PMID:33058343 1322967 Kpna4 karyopherin subunit alpha 4 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20210311 MGI PMID:32320654 1322970 Parvb parvin, beta gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20160804 MGI 1322970 Parvb parvin, beta gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20141003 MGI 1322970 Parvb parvin, beta gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1322970 Parvb parvin, beta gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1322970 Parvb parvin, beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18662549 1322970 Parvb parvin, beta gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1322970 Parvb parvin, beta gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20160804 MGI 1322970 Parvb parvin, beta gene MP:0005018 decreased T cell number IEA N RGD:5509061 20141003 MGI 1322970 Parvb parvin, beta gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20141003 MGI 1322970 Parvb parvin, beta gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20141003 MGI 1322970 Parvb parvin, beta gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20141003 MGI 1322970 Parvb parvin, beta gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20160804 MGI 1322970 Parvb parvin, beta gene MP:0008211 decreased mature B cell number IEA N RGD:5509061 20141003 MGI 1322972 Plekho1 pleckstrin homology domain containing, family O member 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:18641638 1322972 Plekho1 pleckstrin homology domain containing, family O member 1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:18641638 1322972 Plekho1 pleckstrin homology domain containing, family O member 1 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:18641638 1322974 Dnah9 dynein, axonemal, heavy chain 9 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20210729 MGI PMID:33347437 1322974 Dnah9 dynein, axonemal, heavy chain 9 gene MP:0011059 abnormal ependyma motile cilium morphology IAGP N RGD:5509061 20210729 MGI PMID:33347437 1322978 Hinfp histone H4 transcription factor gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:19590016 1322978 Hinfp histone H4 transcription factor gene MP:0003695 delayed blastocyst hatching from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:19590016 1322978 Hinfp histone H4 transcription factor gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19590016 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000498 absent jejunum IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:12468647 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000526 small inner medullary pyramid IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000526 small inner medullary pyramid IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:14671317 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141204 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:10903183 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:11044465 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:12468647 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20170309 MGI PMID:26963625 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12468647 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002163 abnormal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21885021 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002294 short gestation period IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12468647 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12468647 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:12468647 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20170309 MGI PMID:26963625 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003154 abnormal soft palate morphology IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003158 dysphagia IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12468647 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10903183 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003568 uterus atresia IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003572 abnormal uterus development IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003613 abnormal kidney medulla development IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003613 abnormal kidney medulla development IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003756 abnormal hard palate morphology IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:16702402 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141204 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11044465 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12468647 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004260 enlarged placenta IAGP N RGD:5509061 20141003 MGI PMID:11044465 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21885021 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004894 uterus atrophy IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:12468647 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12468647 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12468647 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12468647 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0006320 abnormal interscapular fat pad morphology IAGP N RGD:5509061 20170309 MGI PMID:26963625 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20160609 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20160609 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0008794 increased lens epithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0009709 hydrometra IAGP N RGD:5509061 20141204 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0009735 abnormal prostate gland development IAGP N RGD:5509061 20141204 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21885021 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16702402 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170309 MGI PMID:26963625 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19276117 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11737597 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9136926 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9925645 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20141003 MGI PMID:21885021 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:9144284 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0012503 increased midbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14671317 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0013317 abnormal seminal vesicle development IAGP N RGD:5509061 20141204 MGI PMID:10731669 1322981 Cdkn1c cyclin dependent kinase inhibitor 1C gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10731669 1322983 Cnot9 CCR4-NOT transcription complex, subunit 9 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:22384391 1322983 Cnot9 CCR4-NOT transcription complex, subunit 9 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:22384391 1322983 Cnot9 CCR4-NOT transcription complex, subunit 9 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:22384391 1322983 Cnot9 CCR4-NOT transcription complex, subunit 9 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:22384391 1322985 Spock1 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16806869 1322985 Spock1 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1322985 Spock1 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1322985 Spock1 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1322985 Spock1 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1322985 Spock1 sparc/osteonectin, cwcv and kazal-like domains proteoglycan 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1322987 Stam2 signal transducing adaptor molecule (SH3 domain and ITAM motif) 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12446783 1322987 Stam2 signal transducing adaptor molecule (SH3 domain and ITAM motif) 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22143071 1322987 Stam2 signal transducing adaptor molecule (SH3 domain and ITAM motif) 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12446783 1322987 Stam2 signal transducing adaptor molecule (SH3 domain and ITAM motif) 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12446783 1322987 Stam2 signal transducing adaptor molecule (SH3 domain and ITAM motif) 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12446783 1322989 Slc25a17 solute carrier family 25 (mitochondrial carrier, peroxisomal membrane protein), member 17 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20210422 MGI PMID:32266253 1322989 Slc25a17 solute carrier family 25 (mitochondrial carrier, peroxisomal membrane protein), member 17 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20210422 MGI PMID:32266253 1322989 Slc25a17 solute carrier family 25 (mitochondrial carrier, peroxisomal membrane protein), member 17 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20210422 MGI PMID:32266253 1322989 Slc25a17 solute carrier family 25 (mitochondrial carrier, peroxisomal membrane protein), member 17 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20210422 MGI PMID:32266253 1322989 Slc25a17 solute carrier family 25 (mitochondrial carrier, peroxisomal membrane protein), member 17 gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20210422 MGI PMID:32266253 1322989 Slc25a17 solute carrier family 25 (mitochondrial carrier, peroxisomal membrane protein), member 17 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210422 MGI PMID:32266253 1322992 Igsf8 immunoglobulin superfamily, member 8 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20201022 MGI 1322994 Cacfd1 calcium channel flower domain containing 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22362363 1322994 Cacfd1 calcium channel flower domain containing 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20170323 MGI 1322994 Cacfd1 calcium channel flower domain containing 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20170323 MGI 1322994 Cacfd1 calcium channel flower domain containing 1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22362363 1322994 Cacfd1 calcium channel flower domain containing 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20170323 MGI 1322994 Cacfd1 calcium channel flower domain containing 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22362363 1322994 Cacfd1 calcium channel flower domain containing 1 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22362363 1322995 Ston2 stonin 2 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:23345427 1322995 Ston2 stonin 2 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23345427 1322995 Ston2 stonin 2 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:23345427 1322995 Ston2 stonin 2 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:23345427 1322995 Ston2 stonin 2 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:23345427 1322995 Ston2 stonin 2 gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:23345427 1322995 Ston2 stonin 2 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:23345427 1322995 Ston2 stonin 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:23345427 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0000041 absent endolymphatic duct IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:17591776 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17591776 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0001394 circling IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17591776 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17591776 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0001967 deafness IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17591776 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17591776 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17591776 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0002730 head shaking IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:17591776 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0003169 abnormal scala media morphology IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:14701727 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:17591776 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0004369 absent utricle IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:17591776 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:17591776 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:14701727 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20180927 MGI PMID:17591776 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0006013 absent endolymphatic sac IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17591776 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14701727 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20180215 MGI PMID:29301908 1323001 Slc25a13 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 gene MP:0030742 increased aspartic acid level IAGP N RGD:5509061 20180927 MGI PMID:17591776 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:11784089 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11967219 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21183592 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21183592 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11784089 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11967219 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11784089 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9593760 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21183592 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11784089 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11784089 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11967219 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:21183592 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:21183592 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9593760 1323008 Inpp5b inositol polyphosphate-5-phosphatase B gene MP:0011555 increased urine microglobulin level IAGP N RGD:5509061 20141003 MGI PMID:21183592 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20201002 MGI PMID:32541879 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20220127 MGI PMID:28506985 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0001127 small ovary IAGP N RGD:5509061 20220127 MGI PMID:28506985 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220127 MGI PMID:28506985 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17967868 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17967868 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20201002 MGI PMID:32541879 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0001926 female infertility IAGP N RGD:5509061 20220127 MGI PMID:28506985 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20220127 MGI PMID:28506985 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17967868 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220127 MGI PMID:28506985 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:18541669 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20201002 MGI PMID:32541879 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17967868 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20201002 MGI PMID:32541879 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:18541669 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220127 MGI PMID:28506985 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20201002 MGI PMID:32541879 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20201002 MGI PMID:32541879 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20220127 MGI PMID:28506985 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:17967868 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20201002 MGI PMID:32541879 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0009084 blind uterus IEA N RGD:5509061 20210520 MGI 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18541669 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20201002 MGI PMID:32541879 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17967868 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18541669 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20201002 MGI PMID:32541879 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20220127 MGI PMID:17967868 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:18541669 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0012117 decreased trophectoderm cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18541669 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20220127 MGI PMID:28506985 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0020364 abnormal female germ cell physiology IAGP N RGD:5509061 20220127 MGI PMID:28506985 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220127 MGI PMID:28506985 1323010 Kat8 K(lysine) acetyltransferase 8 gene MP:0031474 increased female germ cell apoptosis IAGP N RGD:5509061 20230615 MGI PMID:28506985 1323014 Trim14 tripartite motif-containing 14 gene MP:0003998 decreased thermal nociceptive threshold IEA N RGD:5509061 20220519 MGI 1323014 Trim14 tripartite motif-containing 14 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20191219 MGI PMID:27666593 1323014 Trim14 tripartite motif-containing 14 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:27666593 1323014 Trim14 tripartite motif-containing 14 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:27666593 1323020 Rab3gap2 RAB3 GTPase activating protein subunit 2 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1323020 Rab3gap2 RAB3 GTPase activating protein subunit 2 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1323020 Rab3gap2 RAB3 GTPase activating protein subunit 2 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201022 MGI 1323020 Rab3gap2 RAB3 GTPase activating protein subunit 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1323020 Rab3gap2 RAB3 GTPase activating protein subunit 2 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1323020 Rab3gap2 RAB3 GTPase activating protein subunit 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1323020 Rab3gap2 RAB3 GTPase activating protein subunit 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1323020 Rab3gap2 RAB3 GTPase activating protein subunit 2 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 1323020 Rab3gap2 RAB3 GTPase activating protein subunit 2 gene MP:0005287 narrow eye opening IEA N RGD:5509061 20201022 MGI 1323020 Rab3gap2 RAB3 GTPase activating protein subunit 2 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20181227 MGI 1323020 Rab3gap2 RAB3 GTPase activating protein subunit 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1323020 Rab3gap2 RAB3 GTPase activating protein subunit 2 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20201231 MGI 1323020 Rab3gap2 RAB3 GTPase activating protein subunit 2 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20181227 MGI 1323024 Eif3e eukaryotic translation initiation factor 3, subunit E gene MP:0000601 small liver IAGP N RGD:5509061 20190516 MGI PMID:30087825 1323024 Eif3e eukaryotic translation initiation factor 3, subunit E gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190516 MGI PMID:30087825 1323024 Eif3e eukaryotic translation initiation factor 3, subunit E gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20190516 MGI PMID:30087825 1323024 Eif3e eukaryotic translation initiation factor 3, subunit E gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20190516 MGI PMID:30087825 1323024 Eif3e eukaryotic translation initiation factor 3, subunit E gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20190516 MGI PMID:30087825 1323024 Eif3e eukaryotic translation initiation factor 3, subunit E gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20190516 MGI PMID:30087825 1323024 Eif3e eukaryotic translation initiation factor 3, subunit E gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1323024 Eif3e eukaryotic translation initiation factor 3, subunit E gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20190516 MGI PMID:30087825 1323024 Eif3e eukaryotic translation initiation factor 3, subunit E gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20190516 MGI PMID:30087825 1323024 Eif3e eukaryotic translation initiation factor 3, subunit E gene MP:0013272 abnormal translation IAGP N RGD:5509061 20190516 MGI PMID:30087825 1323026 Xpo5 exportin 5 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1323026 Xpo5 exportin 5 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1323026 Xpo5 exportin 5 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1323026 Xpo5 exportin 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1323026 Xpo5 exportin 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1323026 Xpo5 exportin 5 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 1323026 Xpo5 exportin 5 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1323026 Xpo5 exportin 5 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210128 MGI 1323026 Xpo5 exportin 5 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1323026 Xpo5 exportin 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1323026 Xpo5 exportin 5 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1323026 Xpo5 exportin 5 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1323026 Xpo5 exportin 5 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210826 MGI 1323026 Xpo5 exportin 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323026 Xpo5 exportin 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1323026 Xpo5 exportin 5 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1323027 Galnt9 polypeptide N-acetylgalactosaminyltransferase 9 gene MP:0001314 cornea opacity IEA N RGD:5509061 20220519 MGI 1323030 Nup93 nucleoporin 93 gene MP:0001714 absent trophoblast giant cells IEA N RGD:5509061 20240926 MGI 1323030 Nup93 nucleoporin 93 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20240926 MGI 1323030 Nup93 nucleoporin 93 gene MP:0004964 absent inner cell mass IEA N RGD:5509061 20240926 MGI 1323030 Nup93 nucleoporin 93 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1323030 Nup93 nucleoporin 93 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20221215 MGI 1323037 Tmem108 transmembrane protein 108 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201231 MGI 1323037 Tmem108 transmembrane protein 108 gene MP:0001513 limb grasping IEA N RGD:5509061 20210826 MGI 1323037 Tmem108 transmembrane protein 108 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20170413 MGI PMID:28096412 1323037 Tmem108 transmembrane protein 108 gene MP:0002635 reduced sensorimotor gating IAGP N RGD:5509061 20170413 MGI PMID:28096412 1323037 Tmem108 transmembrane protein 108 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20170413 MGI PMID:28096412 1323037 Tmem108 transmembrane protein 108 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1323037 Tmem108 transmembrane protein 108 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1323037 Tmem108 transmembrane protein 108 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20170413 MGI PMID:28096412 1323037 Tmem108 transmembrane protein 108 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1323037 Tmem108 transmembrane protein 108 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20170413 MGI PMID:28096412 1323037 Tmem108 transmembrane protein 108 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20170413 MGI PMID:28096412 1323037 Tmem108 transmembrane protein 108 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20170413 MGI PMID:28096412 1323037 Tmem108 transmembrane protein 108 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20170413 MGI PMID:28096412 1323037 Tmem108 transmembrane protein 108 gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20170413 MGI PMID:28096412 1323037 Tmem108 transmembrane protein 108 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1323037 Tmem108 transmembrane protein 108 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1323037 Tmem108 transmembrane protein 108 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20170413 MGI PMID:28096412 1323037 Tmem108 transmembrane protein 108 gene MP:0020335 abnormal dentate gyrus neuron dendrite morphology IAGP N RGD:5509061 20170413 MGI PMID:28096412 1323043 Depdc5 DEP domain containing 5 gene MP:0000434 megacephaly IAGP N RGD:5509061 20180524 MGI PMID:29274432 1323043 Depdc5 DEP domain containing 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180524 MGI PMID:29274432 1323043 Depdc5 DEP domain containing 5 gene MP:0001513 limb grasping IAGP N RGD:5509061 20180524 MGI PMID:29274432 1323043 Depdc5 DEP domain containing 5 gene MP:0002064 seizures IAGP N RGD:5509061 20180524 MGI PMID:29274432 1323043 Depdc5 DEP domain containing 5 gene MP:0002083 premature death IAGP N RGD:5509061 20180524 MGI PMID:29274432 1323043 Depdc5 DEP domain containing 5 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20180524 MGI PMID:29274432 1323043 Depdc5 DEP domain containing 5 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20180524 MGI PMID:29274432 1323043 Depdc5 DEP domain containing 5 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1323043 Depdc5 DEP domain containing 5 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20180524 MGI PMID:29274432 1323043 Depdc5 DEP domain containing 5 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20180524 MGI PMID:29274432 1323043 Depdc5 DEP domain containing 5 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20180524 MGI PMID:29274432 1323043 Depdc5 DEP domain containing 5 gene MP:0005238 increased brain size IAGP N RGD:5509061 20180524 MGI PMID:29274432 1323043 Depdc5 DEP domain containing 5 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20160421 MGI 1323043 Depdc5 DEP domain containing 5 gene MP:0005603 neuron hypertrophy IAGP N RGD:5509061 20180524 MGI PMID:29274432 1323043 Depdc5 DEP domain containing 5 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20180524 MGI PMID:29274432 1323043 Depdc5 DEP domain containing 5 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20180524 MGI PMID:29274432 1323043 Depdc5 DEP domain containing 5 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1323043 Depdc5 DEP domain containing 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323050 Ints9 integrator complex subunit 9 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1323050 Ints9 integrator complex subunit 9 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20201022 MGI 1323050 Ints9 integrator complex subunit 9 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1323050 Ints9 integrator complex subunit 9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323052 Rae1 ribonucleic acid export 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12551952 1323052 Rae1 ribonucleic acid export 1 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:16476774 1323052 Rae1 ribonucleic acid export 1 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:16476774 1323052 Rae1 ribonucleic acid export 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16476774 1323052 Rae1 ribonucleic acid export 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:16476774 1323052 Rae1 ribonucleic acid export 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:16476774 1323052 Rae1 ribonucleic acid export 1 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:16476774 1323052 Rae1 ribonucleic acid export 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:12551952 1323052 Rae1 ribonucleic acid export 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:16476774 1323052 Rae1 ribonucleic acid export 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:12551952 1323052 Rae1 ribonucleic acid export 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:16476774 1323052 Rae1 ribonucleic acid export 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20191205 MGI PMID:26731471 1323052 Rae1 ribonucleic acid export 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:12551952 1323052 Rae1 ribonucleic acid export 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:16476774 1323052 Rae1 ribonucleic acid export 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20191205 MGI PMID:26731471 1323052 Rae1 ribonucleic acid export 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:12551952 1323052 Rae1 ribonucleic acid export 1 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:12551952 1323052 Rae1 ribonucleic acid export 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:16476774 1323052 Rae1 ribonucleic acid export 1 gene MP:0008007 abnormal cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:16476774 1323052 Rae1 ribonucleic acid export 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16476774 1323052 Rae1 ribonucleic acid export 1 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20191205 MGI PMID:26731471 1323052 Rae1 ribonucleic acid export 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16476774 1323052 Rae1 ribonucleic acid export 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12551952 1323052 Rae1 ribonucleic acid export 1 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:16476774 1323054 Mmp17 matrix metallopeptidase 17 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1323054 Mmp17 matrix metallopeptidase 17 gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:21347258 1323054 Mmp17 matrix metallopeptidase 17 gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:21347258 1323054 Mmp17 matrix metallopeptidase 17 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:21347258 1323054 Mmp17 matrix metallopeptidase 17 gene MP:0008055 increased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:21347258 1323054 Mmp17 matrix metallopeptidase 17 gene MP:0010981 abnormal branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:21347258 1323054 Mmp17 matrix metallopeptidase 17 gene MP:0011737 hypodipsia IAGP N RGD:5509061 20141003 MGI PMID:21347258 1323054 Mmp17 matrix metallopeptidase 17 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:21347258 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:22908313 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:9878048 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:10393958 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0008129 absent brain internal capsule IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10393958 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0009026 abnormal brain pia mater morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0009027 abnormal subarachnoid space morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0009586 increased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:9878048 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323056 Vasp vasodilator-stimulated phosphoprotein gene MP:0011724 ectopic cortical neuron IAGP N RGD:5509061 20141003 MGI PMID:17988629 1323064 Sik3 SIK family kinase 3 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0000160 kyphosis IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0000322 increased granulocyte number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0000341 abnormal bile color IAGP N RGD:5509061 20200116 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0000552 abnormal radius morphology IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0000610 cholestasis IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20201022 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0002187 abnormal fibula morphology IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0003947 abnormal cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20200116 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0004892 increased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0004974 decreased regulatory T cell number IEA N RGD:5509061 20201022 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20161124 MGI PMID:27806374 1323064 Sik3 SIK family kinase 3 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0005084 abnormal gallbladder morphology IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0005108 abnormal ulna morphology IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0005270 abnormal zygomatic bone morphology IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0008173 increased follicular B cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0008178 decreased germinal center B cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0008347 decreased gamma-delta T cell number IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0008524 increased plasmacytoid dendritic cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0009109 decreased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0009303 decreased renal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0009342 enlarged gallbladder IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0009492 abnormal gallbladder epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0010099 abnormal thoracic cage shape IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0011016 increased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0011234 abnormal retinol level IAGP N RGD:5509061 20141003 MGI PMID:22662228 1323064 Sik3 SIK family kinase 3 gene MP:0011504 abnormal limb long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0012288 abnormal paradoxical sleep pattern IAGP N RGD:5509061 20161124 MGI PMID:27806374 1323064 Sik3 SIK family kinase 3 gene MP:0012289 abnormal non-rapid eye movement sleep pattern IAGP N RGD:5509061 20161124 MGI PMID:27806374 1323064 Sik3 SIK family kinase 3 gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0012768 decreased KLRG1-positive NK cell number IEA N RGD:5509061 20181227 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013154 increased KLRG1+ CD8 alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013418 increased memory-marker gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013420 decreased CD5-positive gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013427 increased memory-marker NK cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013433 increased KLRG1-positive CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013436 increased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013511 increased CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013513 decreased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013517 increased KLRG1-positive CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013519 decreased CD4-positive NK T cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013522 decreased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013675 decreased Ly6C-positive mature NK cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013679 increased Ly6C-positive NK T cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013683 decreased early germinal center B cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013764 decreased T-helper cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013771 decreased effector memory T-helper cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013774 decreased KLRG1-positive T-helper cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0013775 increased KLRG1-positive T-helper cell number IEA N RGD:5509061 20201231 MGI 1323064 Sik3 SIK family kinase 3 gene MP:0020478 abnormal circadian sleep/wake cycle IAGP N RGD:5509061 20171012 MGI PMID:27806374 1323064 Sik3 SIK family kinase 3 gene MP:0021198 abnormal sleep duration IAGP N RGD:5509061 20220922 MGI PMID:27806374 1323064 Sik3 SIK family kinase 3 gene MP:0030388 large fontanelles IAGP N RGD:5509061 20171207 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0030884 rachitic rosary IAGP N RGD:5509061 20181101 MGI PMID:22318228 1323064 Sik3 SIK family kinase 3 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:22662228 1323069 Amfr autocrine motility factor receptor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20160107 MGI PMID:25789613 1323069 Amfr autocrine motility factor receptor gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20160107 MGI PMID:25789613 1323069 Amfr autocrine motility factor receptor gene MP:0001261 obese IAGP N RGD:5509061 20160107 MGI PMID:25789613 1323069 Amfr autocrine motility factor receptor gene MP:0001860 liver inflammation IAGP N RGD:5509061 20160107 MGI PMID:25789613 1323069 Amfr autocrine motility factor receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160107 MGI PMID:25789613 1323069 Amfr autocrine motility factor receptor gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1323069 Amfr autocrine motility factor receptor gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1323069 Amfr autocrine motility factor receptor gene MP:0003046 liver cirrhosis IAGP N RGD:5509061 20160107 MGI PMID:25789613 1323069 Amfr autocrine motility factor receptor gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20160107 MGI PMID:25789613 1323069 Amfr autocrine motility factor receptor gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160804 MGI 1323069 Amfr autocrine motility factor receptor gene MP:0005571 decreased lactate dehydrogenase level IEA N RGD:5509061 20160804 MGI 1323069 Amfr autocrine motility factor receptor gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 1323069 Amfr autocrine motility factor receptor gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20160107 MGI PMID:25789613 1323069 Amfr autocrine motility factor receptor gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20160107 MGI PMID:25789613 1323069 Amfr autocrine motility factor receptor gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20160804 MGI 1323076 Usp28 ubiquitin specific peptidase 28 gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20151210 MGI PMID:24687851 1323076 Usp28 ubiquitin specific peptidase 28 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20151210 MGI PMID:24687851 1323076 Usp28 ubiquitin specific peptidase 28 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20151210 MGI PMID:24687851 1323078 Vps18 VPS18 CORVET/HOPS core subunit gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:22854957 1323078 Vps18 VPS18 CORVET/HOPS core subunit gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:22854957 1323078 Vps18 VPS18 CORVET/HOPS core subunit gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:22854957 1323078 Vps18 VPS18 CORVET/HOPS core subunit gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:22854957 1323078 Vps18 VPS18 CORVET/HOPS core subunit gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:22854957 1323078 Vps18 VPS18 CORVET/HOPS core subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22854957 1323078 Vps18 VPS18 CORVET/HOPS core subunit gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22854957 1323078 Vps18 VPS18 CORVET/HOPS core subunit gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22854957 1323078 Vps18 VPS18 CORVET/HOPS core subunit gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22854957 1323078 Vps18 VPS18 CORVET/HOPS core subunit gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22854957 1323078 Vps18 VPS18 CORVET/HOPS core subunit gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:22854957 1323078 Vps18 VPS18 CORVET/HOPS core subunit gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:22854957 1323078 Vps18 VPS18 CORVET/HOPS core subunit gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:22854957 1323078 Vps18 VPS18 CORVET/HOPS core subunit gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22854957 1323078 Vps18 VPS18 CORVET/HOPS core subunit gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22854957 1323080 Rnf25 ring finger protein 25 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1323080 Rnf25 ring finger protein 25 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20160421 MGI 1323080 Rnf25 ring finger protein 25 gene MP:0001523 impaired righting response IEA N RGD:5509061 20181227 MGI 1323080 Rnf25 ring finger protein 25 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1323080 Rnf25 ring finger protein 25 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 1323080 Rnf25 ring finger protein 25 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20170105 MGI 1323080 Rnf25 ring finger protein 25 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1323080 Rnf25 ring finger protein 25 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1323081 Shtn1 shootin 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20190919 MGI PMID:30082022 1323081 Shtn1 shootin 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20190919 MGI PMID:30082022 1323081 Shtn1 shootin 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20190919 MGI PMID:30082022 1323081 Shtn1 shootin 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1323081 Shtn1 shootin 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1323081 Shtn1 shootin 1 gene MP:0008222 decreased hippocampal commissure size IAGP N RGD:5509061 20190919 MGI PMID:30082022 1323081 Shtn1 shootin 1 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20190919 MGI PMID:30082022 1323081 Shtn1 shootin 1 gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20190919 MGI PMID:30082022 1323081 Shtn1 shootin 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20190919 MGI PMID:30082022 1323081 Shtn1 shootin 1 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20190919 MGI PMID:30082022 1323081 Shtn1 shootin 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20190919 MGI PMID:30082022 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0000745 tremors IEA N RGD:5509061 20220811 MGI 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20210506 MGI PMID:32245241 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20210506 MGI PMID:32245241 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20220519 MGI 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20210506 MGI PMID:32245241 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20210506 MGI PMID:32245241 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20210506 MGI PMID:32245241 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220519 MGI 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20210506 MGI PMID:32245241 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20210506 MGI PMID:32245241 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20210506 MGI PMID:32245241 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0009392 retina gliosis IAGP N RGD:5509061 20210415 MGI PMID:32272552 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20210506 MGI PMID:32245241 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0010452 retina microaneurysm IAGP N RGD:5509061 20210506 MGI PMID:32245241 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20210506 MGI PMID:32245241 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20210506 MGI PMID:32245241 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20210506 MGI PMID:32245241 1323084 Dhdds dehydrodolichyl diphosphate synthase gene MP:0031141 increased retina vascular tortuosity IAGP N RGD:5509061 20210506 MGI PMID:32245241 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20161201 MGI PMID:25251415 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0003742 narrow head IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0004340 short scapula IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0004576 abnormal embryonic autopod plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0011261 abnormal limb mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:21750036 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:25251415 1323088 2700049A03Rik RIKEN cDNA 2700049A03 gene gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:21750036 1323089 Stt3b STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae) gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1323089 Stt3b STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae) gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1323089 Stt3b STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae) gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1323089 Stt3b STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae) gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20220519 MGI 1323089 Stt3b STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae) gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1323089 Stt3b STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae) gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1323089 Stt3b STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae) gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1323089 Stt3b STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1323089 Stt3b STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae) gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220811 MGI 1323094 Cdc42ep4 CDC42 effector protein 4 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20171012 MGI PMID:26657011 1323094 Cdc42ep4 CDC42 effector protein 4 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20171012 MGI PMID:26657011 1323094 Cdc42ep4 CDC42 effector protein 4 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20171012 MGI PMID:26657011 1323094 Cdc42ep4 CDC42 effector protein 4 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20171012 MGI PMID:26657011 1323094 Cdc42ep4 CDC42 effector protein 4 gene MP:0011002 enhanced AMPA-mediated synaptic currents IAGP N RGD:5509061 20171012 MGI PMID:26657011 1323094 Cdc42ep4 CDC42 effector protein 4 gene MP:0011273 prolonged excitatory postsynaptic current decay time IAGP N RGD:5509061 20171012 MGI PMID:26657011 1323100 Dgkd diacylglycerol kinase, delta gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:17021016 1323100 Dgkd diacylglycerol kinase, delta gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17021016 1323100 Dgkd diacylglycerol kinase, delta gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17357084 1323100 Dgkd diacylglycerol kinase, delta gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17357084 1323100 Dgkd diacylglycerol kinase, delta gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:17357084 1323100 Dgkd diacylglycerol kinase, delta gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1323100 Dgkd diacylglycerol kinase, delta gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:17021016 1323100 Dgkd diacylglycerol kinase, delta gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:17021016 1323100 Dgkd diacylglycerol kinase, delta gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1323100 Dgkd diacylglycerol kinase, delta gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17021016 1323100 Dgkd diacylglycerol kinase, delta gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:17021016 1323100 Dgkd diacylglycerol kinase, delta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17021016 1323100 Dgkd diacylglycerol kinase, delta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1323100 Dgkd diacylglycerol kinase, delta gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1323103 Mmp28 matrix metallopeptidase 28 (epilysin) gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:19265166 1323103 Mmp28 matrix metallopeptidase 28 (epilysin) gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:19265166 1323103 Mmp28 matrix metallopeptidase 28 (epilysin) gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19265166 1323103 Mmp28 matrix metallopeptidase 28 (epilysin) gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:19265166 1323103 Mmp28 matrix metallopeptidase 28 (epilysin) gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:19265166 1323103 Mmp28 matrix metallopeptidase 28 (epilysin) gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:19265166 1323103 Mmp28 matrix metallopeptidase 28 (epilysin) gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:19265166 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0000467 abnormal esophagus morphology IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0000648 absent sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0000763 abnormal filiform papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12944479 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12944479 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:12944479 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0003155 abnormal telomere length IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0003751 oral leukoplakia IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:12944479 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:19596237 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12944479 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19679647 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12944479 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12944479 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:12944479 1323105 Terf1 telomeric repeat binding factor 1 gene MP:0030926 increased skin pigmentation IAGP N RGD:5509061 20190117 MGI PMID:19679647 1323106 Cracd capping protein inhibiting regulator of actin gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20201022 MGI 1323106 Cracd capping protein inhibiting regulator of actin gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1323110 Ndufaf7 NADH:ubiquinone oxidoreductase complex assembly factor 7 gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20141218 MGI PMID:24838397 1323112 E2f4 E2F transcription factor 4 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0000346 broad head IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0001400 hyperresponsive IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0001867 rhinitis IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20160218 MGI PMID:26825228 1323112 E2f4 E2F transcription factor 4 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12498715 1323112 E2f4 E2F transcription factor 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12498715 1323112 E2f4 E2F transcription factor 4 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160218 MGI PMID:26825228 1323112 E2f4 E2F transcription factor 4 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0002244 abnormal turbinate morphology IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:12498715 1323112 E2f4 E2F transcription factor 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0002424 abnormal reticulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20160218 MGI PMID:26825228 1323112 E2f4 E2F transcription factor 4 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:11030352 1323112 E2f4 E2F transcription factor 4 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0004728 abnormal efferent ductules of testis morphology IAGP N RGD:5509061 20160218 MGI PMID:26825228 1323112 E2f4 E2F transcription factor 4 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0006423 dilated rete testis IAGP N RGD:5509061 20160218 MGI PMID:26825228 1323112 E2f4 E2F transcription factor 4 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0009257 dilated seminiferous tubule IAGP N RGD:5509061 20160218 MGI PMID:26825228 1323112 E2f4 E2F transcription factor 4 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0010178 increased number of Howell-Jolly bodies IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0010178 increased number of Howell-Jolly bodies IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12498715 1323112 E2f4 E2F transcription factor 4 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12498715 1323112 E2f4 E2F transcription factor 4 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20170803 MGI PMID:28675157 1323112 E2f4 E2F transcription factor 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11030352 1323112 E2f4 E2F transcription factor 4 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20160218 MGI PMID:26825228 1323112 E2f4 E2F transcription factor 4 gene MP:0013792 abnormal small intestine goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:10983977 1323112 E2f4 E2F transcription factor 4 gene MP:0030189 broad snout IAGP N RGD:5509061 20171019 MGI PMID:10983976 1323112 E2f4 E2F transcription factor 4 gene MP:0031276 abnormal stress erythropoiesis IAGP N RGD:5509061 20210805 MGI PMID:10983976 1323114 Zbtb48 zinc finger and BTB domain containing 48 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1323114 Zbtb48 zinc finger and BTB domain containing 48 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1323114 Zbtb48 zinc finger and BTB domain containing 48 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1323114 Zbtb48 zinc finger and BTB domain containing 48 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210520 MGI 1323114 Zbtb48 zinc finger and BTB domain containing 48 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20201022 MGI 1323114 Zbtb48 zinc finger and BTB domain containing 48 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1323114 Zbtb48 zinc finger and BTB domain containing 48 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20231207 MGI 1323114 Zbtb48 zinc finger and BTB domain containing 48 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1323116 Ubn1 ubinuclein 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1323116 Ubn1 ubinuclein 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20181227 MGI 1323116 Ubn1 ubinuclein 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1323116 Ubn1 ubinuclein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1323118 Tead3 TEA domain family member 3 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20181227 MGI 1323118 Tead3 TEA domain family member 3 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1323118 Tead3 TEA domain family member 3 gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20181227 MGI 1323118 Tead3 TEA domain family member 3 gene MP:0010869 decreased bone trabecula number IEA N RGD:5509061 20210128 MGI 1323118 Tead3 TEA domain family member 3 gene MP:0013630 increased bone trabecular spacing IEA N RGD:5509061 20211021 MGI 1323119 Stap1 signal transducing adaptor family member 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1323119 Stap1 signal transducing adaptor family member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200903 MGI PMID:31996024 1323121 Vrk2 vaccinia related kinase 2 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20240307 MGI PMID:37452335 1323121 Vrk2 vaccinia related kinase 2 gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20240307 MGI PMID:37452335 1323121 Vrk2 vaccinia related kinase 2 gene MP:0020512 abnormal dendritic mushroom spine morphology IAGP N RGD:5509061 20240307 MGI PMID:37452335 1323121 Vrk2 vaccinia related kinase 2 gene MP:0020514 abnormal dendritic thin spine morphology IAGP N RGD:5509061 20240307 MGI PMID:37452335 1323121 Vrk2 vaccinia related kinase 2 gene MP:0021010 impaired synaptic physiology IAGP N RGD:5509061 20240307 MGI PMID:37452335 1323123 Ptpn18 protein tyrosine phosphatase, non-receptor type 18 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1323123 Ptpn18 protein tyrosine phosphatase, non-receptor type 18 gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 1323123 Ptpn18 protein tyrosine phosphatase, non-receptor type 18 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1323123 Ptpn18 protein tyrosine phosphatase, non-receptor type 18 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220519 MGI 1323123 Ptpn18 protein tyrosine phosphatase, non-receptor type 18 gene MP:0006241 abnormal placement of pupils IEA N RGD:5509061 20231207 MGI 1323123 Ptpn18 protein tyrosine phosphatase, non-receptor type 18 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220519 MGI 1323123 Ptpn18 protein tyrosine phosphatase, non-receptor type 18 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210520 MGI 1323126 Riok2 RIO kinase 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170504 MGI 1323126 Riok2 RIO kinase 2 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0001577 anemia IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1323126 Riok2 RIO kinase 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1323126 Riok2 RIO kinase 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20231207 MGI 1323126 Riok2 RIO kinase 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1323126 Riok2 RIO kinase 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1323126 Riok2 RIO kinase 2 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1323126 Riok2 RIO kinase 2 gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323126 Riok2 RIO kinase 2 gene MP:0013696 increased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16200209 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16200209 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16200209 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16200209 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:16368888 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:16200209 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:18083848 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:16200209 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:16368888 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:16200209 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:16368888 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18083848 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18083848 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201002 MGI PMID:18083848 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:19109562 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20201001 MGI PMID:18083848 1323133 Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13 gene MP:0031165 increased circulating von Willebrand factor level IAGP N RGD:5509061 20201015 MGI PMID:16200209 1323137 Mybpc2 myosin binding protein C, fast-type gene MP:0000747 muscle weakness IAGP N RGD:5509061 20240718 MGI PMID:33888578 1323137 Mybpc2 myosin binding protein C, fast-type gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20240718 MGI PMID:33888578 1323137 Mybpc2 myosin binding protein C, fast-type gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20240718 MGI PMID:33888578 1323137 Mybpc2 myosin binding protein C, fast-type gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20240718 MGI PMID:33888578 1323137 Mybpc2 myosin binding protein C, fast-type gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20240718 MGI PMID:33888578 1323137 Mybpc2 myosin binding protein C, fast-type gene MP:0004144 hypotonia IAGP N RGD:5509061 20240718 MGI PMID:33888578 1323137 Mybpc2 myosin binding protein C, fast-type gene MP:0004246 abnormal extensor digitorum longus morphology IAGP N RGD:5509061 20240718 MGI PMID:33888578 1323137 Mybpc2 myosin binding protein C, fast-type gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20240718 MGI PMID:33888578 1323137 Mybpc2 myosin binding protein C, fast-type gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20240718 MGI PMID:33888578 1323137 Mybpc2 myosin binding protein C, fast-type gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20240718 MGI PMID:33888578 1323137 Mybpc2 myosin binding protein C, fast-type gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20240718 MGI PMID:33888578 1323139 Cers5 ceramide synthase 5 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210520 MGI 1323139 Cers5 ceramide synthase 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1323139 Cers5 ceramide synthase 5 gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20201231 MGI 1323139 Cers5 ceramide synthase 5 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201022 MGI 1323139 Cers5 ceramide synthase 5 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1323139 Cers5 ceramide synthase 5 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1323139 Cers5 ceramide synthase 5 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220811 MGI 1323141 Sin3a transcriptional regulator, SIN3A (yeast) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15998811 1323141 Sin3a transcriptional regulator, SIN3A (yeast) gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15998811 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:20407208 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:20407208 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20407208 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:20713727 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20160929 MGI PMID:24557352 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:20407208 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:20407208 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20160929 MGI PMID:24557352 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0002546 mydriasis IEA N RGD:5509061 20181227 MGI 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20713727 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:20713727 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20713727 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20713727 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:20713727 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20141003 MGI PMID:20407208 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20713727 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20181227 MGI 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:20713727 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:20713727 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:20713727 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20160929 MGI PMID:24557352 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20160929 MGI PMID:24557352 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20160929 MGI PMID:24557352 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20407208 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20160929 MGI PMID:24557352 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20160929 MGI PMID:24557352 1323142 Lpcat1 lysophosphatidylcholine acyltransferase 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20160929 MGI PMID:24557352 1323143 Zfp474 zinc finger protein 474 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1323143 Zfp474 zinc finger protein 474 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1323143 Zfp474 zinc finger protein 474 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1323143 Zfp474 zinc finger protein 474 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210520 MGI 1323143 Zfp474 zinc finger protein 474 gene MP:0001147 small testis IEA N RGD:5509061 20210520 MGI 1323143 Zfp474 zinc finger protein 474 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1323143 Zfp474 zinc finger protein 474 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20210520 MGI 1323143 Zfp474 zinc finger protein 474 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20210520 MGI 1323143 Zfp474 zinc finger protein 474 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1323143 Zfp474 zinc finger protein 474 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210520 MGI 1323144 Fastk Fas-activated serine/threonine kinase gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20363972 1323144 Fastk Fas-activated serine/threonine kinase gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:20363972 1323144 Fastk Fas-activated serine/threonine kinase gene MP:0002833 increased heart weight IEA N RGD:5509061 20231207 MGI 1323144 Fastk Fas-activated serine/threonine kinase gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 1323144 Fastk Fas-activated serine/threonine kinase gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20363972 1323144 Fastk Fas-activated serine/threonine kinase gene MP:0008691 decreased interleukin-23 secretion IAGP N RGD:5509061 20141003 MGI PMID:20363972 1323144 Fastk Fas-activated serine/threonine kinase gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20363972 1323144 Fastk Fas-activated serine/threonine kinase gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20363972 1323144 Fastk Fas-activated serine/threonine kinase gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20363972 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17145776 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0000525 renal tubular acidosis IAGP N RGD:5509061 20160707 MGI PMID:26068853 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17145776 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17145776 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17145776 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17145776 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17145776 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0001957 apnea IAGP N RGD:5509061 20160707 MGI PMID:26068853 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0002318 hypercapnia IAGP N RGD:5509061 20160707 MGI PMID:26068853 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20160707 MGI PMID:26068853 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20160707 MGI PMID:26068853 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0003031 acidosis IAGP N RGD:5509061 20160707 MGI PMID:26068853 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20160707 MGI PMID:22045552 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20160707 MGI PMID:26068853 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0003620 oliguria IAGP N RGD:5509061 20160707 MGI PMID:26068853 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17145776 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:17145776 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0005488 bronchial epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17145776 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0005576 decreased pulmonary ventilation IAGP N RGD:5509061 20160707 MGI PMID:26068853 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17145776 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20160707 MGI PMID:22045552 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0008055 increased urine osmolality IAGP N RGD:5509061 20160707 MGI PMID:26068853 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0008816 petechiae IAGP N RGD:5509061 20141003 MGI PMID:17145776 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20160707 MGI PMID:22045552 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17145776 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17145776 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0011428 decreased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:17145776 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0011437 glomerulus hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17145776 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0011470 increased urine creatinine level IAGP N RGD:5509061 20160707 MGI PMID:26068853 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0011735 increased urine ammonia level IAGP N RGD:5509061 20160707 MGI PMID:26068853 1323149 Gpr4 G protein-coupled receptor 4 gene MP:0014273 abnormal skin vasculature morphology IAGP N RGD:5509061 20230810 MGI PMID:17145776 1323151 Atraid all-trans retinoic acid induced differentiation factor gene MP:0001304 cataract IEA N RGD:5509061 20141003 MGI 1323154 Mcrs1 microspherule protein 1 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20240613 MGI PMID:31671403 1323154 Mcrs1 microspherule protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160818 MGI PMID:25816988 1323154 Mcrs1 microspherule protein 1 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20240613 MGI PMID:31671403 1323154 Mcrs1 microspherule protein 1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20220519 MGI 1323154 Mcrs1 microspherule protein 1 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20240613 MGI PMID:31671403 1323154 Mcrs1 microspherule protein 1 gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20240801 MGI PMID:31671403 1323154 Mcrs1 microspherule protein 1 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20240613 MGI PMID:31671403 1323154 Mcrs1 microspherule protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160818 MGI PMID:25816988 1323154 Mcrs1 microspherule protein 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20240801 MGI PMID:31671403 1323154 Mcrs1 microspherule protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323154 Mcrs1 microspherule protein 1 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20240801 MGI PMID:31671403 1323154 Mcrs1 microspherule protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1323156 Taf6 TATA-box binding protein associated factor 6 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1323156 Taf6 TATA-box binding protein associated factor 6 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1323156 Taf6 TATA-box binding protein associated factor 6 gene MP:0006204 embryonic lethality before implantation IEA N RGD:5509061 20111116 MGI 1323156 Taf6 TATA-box binding protein associated factor 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323156 Taf6 TATA-box binding protein associated factor 6 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1323156 Taf6 TATA-box binding protein associated factor 6 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1323158 Hsph1 heat shock 105kDa/110kDa protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20150917 MGI PMID:18658041 1323158 Hsph1 heat shock 105kDa/110kDa protein 1 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20150917 MGI PMID:18658041 1323158 Hsph1 heat shock 105kDa/110kDa protein 1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20150917 MGI PMID:18658041 1323160 Cd22 CD22 antigen gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 1323160 Cd22 CD22 antigen gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:23836650 1323160 Cd22 CD22 antigen gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1323160 Cd22 CD22 antigen gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220811 MGI 1323160 Cd22 CD22 antigen gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:23836650 1323160 Cd22 CD22 antigen gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:8864124 1323160 Cd22 CD22 antigen gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20111116 MGI 1323160 Cd22 CD22 antigen gene MP:0001802 arrested B cell differentiation IEA N RGD:5509061 20111116 MGI 1323160 Cd22 CD22 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1323160 Cd22 CD22 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:8967951 1323160 Cd22 CD22 antigen gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:23836650 1323160 Cd22 CD22 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10209047 1323160 Cd22 CD22 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22761313 1323160 Cd22 CD22 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22965838 1323160 Cd22 CD22 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23836650 1323160 Cd22 CD22 antigen gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:8864124 1323160 Cd22 CD22 antigen gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:10209047 1323160 Cd22 CD22 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:8864124 1323160 Cd22 CD22 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9586639 1323160 Cd22 CD22 antigen gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:10209047 1323160 Cd22 CD22 antigen gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:8864124 1323160 Cd22 CD22 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:17420268 1323160 Cd22 CD22 antigen gene MP:0004944 abnormal B cell negative selection IAGP N RGD:5509061 20141003 MGI PMID:9586639 1323160 Cd22 CD22 antigen gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:8864124 1323160 Cd22 CD22 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15378059 1323160 Cd22 CD22 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22965838 1323160 Cd22 CD22 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23836650 1323160 Cd22 CD22 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:24344237 1323160 Cd22 CD22 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15378059 1323160 Cd22 CD22 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24344237 1323160 Cd22 CD22 antigen gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18354178 1323160 Cd22 CD22 antigen gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8967951 1323160 Cd22 CD22 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15378059 1323160 Cd22 CD22 antigen gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 1323160 Cd22 CD22 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IEA N RGD:5509061 20141225 MGI 1323160 Cd22 CD22 antigen gene MP:0008167 increased B-1a cell number IEA N RGD:5509061 20150507 MGI 1323160 Cd22 CD22 antigen gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1323160 Cd22 CD22 antigen gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8864124 1323160 Cd22 CD22 antigen gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8967951 1323160 Cd22 CD22 antigen gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9586639 1323160 Cd22 CD22 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:15378059 1323160 Cd22 CD22 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1323160 Cd22 CD22 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18354178 1323160 Cd22 CD22 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:22965838 1323160 Cd22 CD22 antigen gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:23836650 1323160 Cd22 CD22 antigen gene MP:0008188 abnormal transitional stage B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18354178 1323160 Cd22 CD22 antigen gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:23836650 1323160 Cd22 CD22 antigen gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20151015 MGI 1323160 Cd22 CD22 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15378059 1323160 Cd22 CD22 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1323160 Cd22 CD22 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18354178 1323160 Cd22 CD22 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:8967951 1323160 Cd22 CD22 antigen gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:23836650 1323160 Cd22 CD22 antigen gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:17420268 1323160 Cd22 CD22 antigen gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:8864124 1323160 Cd22 CD22 antigen gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:8967951 1323160 Cd22 CD22 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:8967951 1323160 Cd22 CD22 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:8967951 1323160 Cd22 CD22 antigen gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:23836650 1323160 Cd22 CD22 antigen gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:10209047 1323160 Cd22 CD22 antigen gene MP:0008729 decreased memory B cell number IAGP N RGD:5509061 20141003 MGI PMID:8967951 1323160 Cd22 CD22 antigen gene MP:0008746 abnormal peripheral B cell anergy IAGP N RGD:5509061 20141003 MGI PMID:24344237 1323160 Cd22 CD22 antigen gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18354178 1323160 Cd22 CD22 antigen gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23836650 1323160 Cd22 CD22 antigen gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1323160 Cd22 CD22 antigen gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22965838 1323160 Cd22 CD22 antigen gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22965838 1323160 Cd22 CD22 antigen gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20180215 MGI 1323160 Cd22 CD22 antigen gene MP:0010674 increased activation-induced B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24344237 1323160 Cd22 CD22 antigen gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20180215 MGI 1323160 Cd22 CD22 antigen gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20141003 MGI PMID:23836650 1323160 Cd22 CD22 antigen gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:22965838 1323160 Cd22 CD22 antigen gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:8864124 1323160 Cd22 CD22 antigen gene MP:0014472 impaired B cell migration IAGP N RGD:5509061 20240613 MGI PMID:22965838 1323162 Cars2 cysteinyl-tRNA synthetase 2, mitochondrial gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20231207 MGI 1323162 Cars2 cysteinyl-tRNA synthetase 2, mitochondrial gene MP:0000745 tremors IEA N RGD:5509061 20111116 MGI 1323162 Cars2 cysteinyl-tRNA synthetase 2, mitochondrial gene MP:0001410 head bobbing IEA N RGD:5509061 20111116 MGI 1323162 Cars2 cysteinyl-tRNA synthetase 2, mitochondrial gene MP:0001513 limb grasping IEA N RGD:5509061 20230601 MGI 1323162 Cars2 cysteinyl-tRNA synthetase 2, mitochondrial gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20231207 MGI 1323162 Cars2 cysteinyl-tRNA synthetase 2, mitochondrial gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20231207 MGI 1323162 Cars2 cysteinyl-tRNA synthetase 2, mitochondrial gene MP:0001914 hemorrhage IEA N RGD:5509061 20231207 MGI 1323162 Cars2 cysteinyl-tRNA synthetase 2, mitochondrial gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20191114 MGI PMID:29079736 1323162 Cars2 cysteinyl-tRNA synthetase 2, mitochondrial gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20231207 MGI 1323162 Cars2 cysteinyl-tRNA synthetase 2, mitochondrial gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20231207 MGI 1323162 Cars2 cysteinyl-tRNA synthetase 2, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20191114 MGI PMID:29079736 1323162 Cars2 cysteinyl-tRNA synthetase 2, mitochondrial gene MP:0008911 induced hyperactivity IEA N RGD:5509061 20111116 MGI 1323162 Cars2 cysteinyl-tRNA synthetase 2, mitochondrial gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1323162 Cars2 cysteinyl-tRNA synthetase 2, mitochondrial gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20231207 MGI 1323164 Spop speckle-type BTB/POZ protein gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1323164 Spop speckle-type BTB/POZ protein gene MP:0000706 small thymus IEA N RGD:5509061 20160811 MGI 1323164 Spop speckle-type BTB/POZ protein gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0002544 brachydactyly IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0002768 small adrenal glands IEA N RGD:5509061 20160811 MGI 1323164 Spop speckle-type BTB/POZ protein gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20811152 1323164 Spop speckle-type BTB/POZ protein gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20811152 1323164 Spop speckle-type BTB/POZ protein gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0004635 short metatarsal bones IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20811152 1323164 Spop speckle-type BTB/POZ protein gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20811152 1323164 Spop speckle-type BTB/POZ protein gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1323164 Spop speckle-type BTB/POZ protein gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20811152 1323164 Spop speckle-type BTB/POZ protein gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:20811152 1323164 Spop speckle-type BTB/POZ protein gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1323164 Spop speckle-type BTB/POZ protein gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:20811152 1323164 Spop speckle-type BTB/POZ protein gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0009488 abnormal pancreatic islet cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20811152 1323164 Spop speckle-type BTB/POZ protein gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 1323164 Spop speckle-type BTB/POZ protein gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20160421 MGI 1323164 Spop speckle-type BTB/POZ protein gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170518 MGI PMID:27930311 1323164 Spop speckle-type BTB/POZ protein gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20811152 1323164 Spop speckle-type BTB/POZ protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1323164 Spop speckle-type BTB/POZ protein gene MP:0011940 decreased food intake IEA N RGD:5509061 20201022 MGI 1323168 Khdc3 KH domain containing 3, subcortical maternal complex member gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:19376971 1323168 Khdc3 KH domain containing 3, subcortical maternal complex member gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19376971 1323168 Khdc3 KH domain containing 3, subcortical maternal complex member gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:19376971 1323170 Itk IL2 inducible T cell kinase gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:16547221 1323170 Itk IL2 inducible T cell kinase gene MP:0000350 abnormal cell proliferation IEA N RGD:5509061 20161201 MGI 1323170 Itk IL2 inducible T cell kinase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220811 MGI 1323170 Itk IL2 inducible T cell kinase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220811 MGI 1323170 Itk IL2 inducible T cell kinase gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210520 MGI 1323170 Itk IL2 inducible T cell kinase gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:9584150 1323170 Itk IL2 inducible T cell kinase gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:19416854 1323170 Itk IL2 inducible T cell kinase gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8777721 1323170 Itk IL2 inducible T cell kinase gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16547221 1323170 Itk IL2 inducible T cell kinase gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16860759 1323170 Itk IL2 inducible T cell kinase gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:12055226 1323170 Itk IL2 inducible T cell kinase gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:8777721 1323170 Itk IL2 inducible T cell kinase gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8777721 1323170 Itk IL2 inducible T cell kinase gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8777721 1323170 Itk IL2 inducible T cell kinase gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:16547221 1323170 Itk IL2 inducible T cell kinase gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:10213685 1323170 Itk IL2 inducible T cell kinase gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:8777721 1323170 Itk IL2 inducible T cell kinase gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8777721 1323170 Itk IL2 inducible T cell kinase gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10213685 1323170 Itk IL2 inducible T cell kinase gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8777721 1323170 Itk IL2 inducible T cell kinase gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IEA N RGD:5509061 20161201 MGI 1323170 Itk IL2 inducible T cell kinase gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:16547221 1323170 Itk IL2 inducible T cell kinase gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0008036 abnormal NK T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12193707 1323170 Itk IL2 inducible T cell kinase gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:12193707 1323170 Itk IL2 inducible T cell kinase gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16860759 1323170 Itk IL2 inducible T cell kinase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10213685 1323170 Itk IL2 inducible T cell kinase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12055226 1323170 Itk IL2 inducible T cell kinase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8777721 1323170 Itk IL2 inducible T cell kinase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9584150 1323170 Itk IL2 inducible T cell kinase gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15345221 1323170 Itk IL2 inducible T cell kinase gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12055226 1323170 Itk IL2 inducible T cell kinase gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16860759 1323170 Itk IL2 inducible T cell kinase gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16860759 1323170 Itk IL2 inducible T cell kinase gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16880398 1323170 Itk IL2 inducible T cell kinase gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16860759 1323170 Itk IL2 inducible T cell kinase gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16880398 1323170 Itk IL2 inducible T cell kinase gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10213685 1323170 Itk IL2 inducible T cell kinase gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:19416854 1323170 Itk IL2 inducible T cell kinase gene MP:0008343 abnormal gamma-delta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19416854 1323170 Itk IL2 inducible T cell kinase gene MP:0008353 increased mature gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19416854 1323170 Itk IL2 inducible T cell kinase gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16860759 1323170 Itk IL2 inducible T cell kinase gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15345221 1323170 Itk IL2 inducible T cell kinase gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19416854 1323170 Itk IL2 inducible T cell kinase gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:19416854 1323170 Itk IL2 inducible T cell kinase gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:15345221 1323170 Itk IL2 inducible T cell kinase gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:19416854 1323170 Itk IL2 inducible T cell kinase gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19009524 1323170 Itk IL2 inducible T cell kinase gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:9584150 1323170 Itk IL2 inducible T cell kinase gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19416854 1323170 Itk IL2 inducible T cell kinase gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15345221 1323170 Itk IL2 inducible T cell kinase gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:15345221 1323170 Itk IL2 inducible T cell kinase gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16880398 1323170 Itk IL2 inducible T cell kinase gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20180215 MGI 1323170 Itk IL2 inducible T cell kinase gene MP:0010839 decreased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20180215 MGI 1323170 Itk IL2 inducible T cell kinase gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1323170 Itk IL2 inducible T cell kinase gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1323170 Itk IL2 inducible T cell kinase gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1323170 Itk IL2 inducible T cell kinase gene MP:0011822 increased CD8-positive, alpha-beta memory T cell proliferation IEA N RGD:5509061 20161201 MGI 1323170 Itk IL2 inducible T cell kinase gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1323171 Dnhd1 dynein heavy chain domain 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220317 MGI PMID:34932939 1323171 Dnhd1 dynein heavy chain domain 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220317 MGI PMID:34932939 1323171 Dnhd1 dynein heavy chain domain 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220317 MGI PMID:34932939 1323171 Dnhd1 dynein heavy chain domain 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220317 MGI PMID:34932939 1323171 Dnhd1 dynein heavy chain domain 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220317 MGI PMID:34932939 1323171 Dnhd1 dynein heavy chain domain 1 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220317 MGI PMID:34932939 1323171 Dnhd1 dynein heavy chain domain 1 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220317 MGI PMID:34932939 1323171 Dnhd1 dynein heavy chain domain 1 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20220317 MGI PMID:34932939 1323171 Dnhd1 dynein heavy chain domain 1 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220317 MGI PMID:34932939 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20170622 MGI PMID:17420276 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20170622 MGI PMID:17420276 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20180215 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:11518968 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11518968 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11518968 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:11518968 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170622 MGI PMID:17420276 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20170622 MGI PMID:17420276 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0001606 impaired hematopoiesis IEA N RGD:5509061 20151126 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0001790 abnormal immune system physiology IEA N RGD:5509061 20141003 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20170622 MGI PMID:17420276 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:22761313 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22431588 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22761313 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:11518968 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18157938 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20170622 MGI PMID:17420276 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12871644 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IEA N RGD:5509061 20190411 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12871644 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002492 decreased IgE level IEA N RGD:5509061 20161201 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20170622 MGI PMID:17420276 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002619 abnormal lymphocyte morphology IEA N RGD:5509061 20190411 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002634 abnormal sensorimotor gating IAGP N RGD:5509061 20170622 MGI PMID:17420276 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0002895 abnormal otolithic membrane morphology IAGP N RGD:5509061 20170622 MGI PMID:17420276 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:18157938 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:11518968 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20170622 MGI PMID:17420276 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20170622 MGI PMID:17420276 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22761313 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20190411 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IEA N RGD:5509061 20141003 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22431588 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18157938 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18157938 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:22431588 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12871644 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0005425 increased macrophage cell number IEA N RGD:5509061 20180215 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20170622 MGI PMID:17420276 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008037 abnormal T cell morphology IEA N RGD:5509061 20141003 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20180215 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20190411 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20111116 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008076 abnormal CD4-positive T cell differentiation IEA N RGD:5509061 20141003 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008077 abnormal CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190613 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20151126 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20111116 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20141003 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008082 increased single-positive T cell number IEA N RGD:5509061 20151126 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008083 decreased single-positive T cell number IEA N RGD:5509061 20151126 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11518968 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22431588 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008169 increased B-1b cell number IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008170 decreased B-1b cell number IEA N RGD:5509061 20190411 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:22431588 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:11518968 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20170622 MGI PMID:27210752 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:22431588 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18157938 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22431588 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20170622 MGI PMID:19103880 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008524 increased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22431588 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:22431588 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:16943182 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:22431588 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18157938 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20170622 MGI PMID:27210752 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190411 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190411 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20190411 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20190411 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20190411 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20161201 MGI 1323175 Dock2 dedicator of cyto-kinesis 2 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:19103880 1323178 Btbd3 BTB domain containing 3 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20200514 MGI 1323178 Btbd3 BTB domain containing 3 gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20200514 MGI 1323178 Btbd3 BTB domain containing 3 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20200813 MGI PMID:31501410 1323178 Btbd3 BTB domain containing 3 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20200813 MGI PMID:31501410 1323178 Btbd3 BTB domain containing 3 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20200813 MGI PMID:31501410 1323178 Btbd3 BTB domain containing 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20200813 MGI PMID:31501410 1323178 Btbd3 BTB domain containing 3 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20200813 MGI PMID:31501410 1323178 Btbd3 BTB domain containing 3 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20200514 MGI 1323178 Btbd3 BTB domain containing 3 gene MP:0005355 enlarged thyroid gland IEA N RGD:5509061 20200514 MGI 1323178 Btbd3 BTB domain containing 3 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20220421 MGI PMID:31501410 1323178 Btbd3 BTB domain containing 3 gene MP:0013890 increased CD8-positive, CD25-positive alpha-beta T cell number IEA N RGD:5509061 20220519 MGI 1323178 Btbd3 BTB domain containing 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:31501410 1323179 Setd1a SET domain containing 1A gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20160804 MGI 1323179 Setd1a SET domain containing 1A gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20141003 MGI 1323179 Setd1a SET domain containing 1A gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1323179 Setd1a SET domain containing 1A gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20141003 MGI 1323179 Setd1a SET domain containing 1A gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:24550110 1323179 Setd1a SET domain containing 1A gene MP:0002635 reduced sensorimotor gating IAGP N RGD:5509061 20221117 MGI PMID:35245111 1323179 Setd1a SET domain containing 1A gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1323179 Setd1a SET domain containing 1A gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1323179 Setd1a SET domain containing 1A gene MP:0003345 decreased rib number IEA N RGD:5509061 20160804 MGI 1323179 Setd1a SET domain containing 1A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24550110 1323179 Setd1a SET domain containing 1A gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1323179 Setd1a SET domain containing 1A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24550110 1323179 Setd1a SET domain containing 1A gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:24550110 1323179 Setd1a SET domain containing 1A gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20221117 MGI PMID:35245111 1323179 Setd1a SET domain containing 1A gene MP:0009710 anhedonia IAGP N RGD:5509061 20221117 MGI PMID:35245111 1323179 Setd1a SET domain containing 1A gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1323179 Setd1a SET domain containing 1A gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24550110 1323179 Setd1a SET domain containing 1A gene MP:0020379 abnormal sucrose solution preference IAGP N RGD:5509061 20221117 MGI PMID:35245111 1323179 Setd1a SET domain containing 1A gene MP:0020421 increased freezing behavior IAGP N RGD:5509061 20221117 MGI PMID:35245111 1323179 Setd1a SET domain containing 1A gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20221117 MGI PMID:35245111 1323179 Setd1a SET domain containing 1A gene MP:0021090 abnormal dendrite arborization pattern IAGP N RGD:5509061 20221117 MGI PMID:35245111 1323179 Setd1a SET domain containing 1A gene MP:0030950 abnormal synaptic vesicle exocytosis IAGP N RGD:5509061 20221117 MGI PMID:35245111 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21723200 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23359070 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21723200 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21723200 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20170223 MGI PMID:27622333 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20170223 MGI PMID:27622333 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21873190 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20170223 MGI PMID:27622333 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21723200 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23359070 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170223 MGI PMID:27622333 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20230316 MGI PMID:35304452 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20230316 MGI PMID:35304452 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21873190 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24218140 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20170223 MGI PMID:27622333 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:23359070 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18288583 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23359070 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24218140 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21873190 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21723200 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20170223 MGI PMID:27622333 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20170223 MGI PMID:27622333 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18288583 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21873190 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20170223 MGI PMID:27622333 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21723200 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170223 MGI PMID:27622333 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20230316 MGI PMID:35304452 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21723200 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21723200 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23359070 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0008112 abnormal monocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21723200 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0008389 hypochromic macrocytic anemia IAGP N RGD:5509061 20170223 MGI PMID:27622333 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20170223 MGI PMID:27622333 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:21873190 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0010129 increased DN1 thymic pro-T cell number IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21723200 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23359070 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20141003 MGI PMID:23359070 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21723200 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21803851 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18288583 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:21723201 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0011181 increased hematopoietic cell number IAGP N RGD:5509061 20141003 MGI PMID:21723200 1323180 Tet2 tet methylcytosine dioxygenase 2 gene MP:0013771 decreased effector memory T-helper cell number IAGP N RGD:5509061 20230316 MGI PMID:35304452 1323182 Ube2k ubiquitin-conjugating enzyme E2K gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18710920 1323187 Dapk1 death associated protein kinase 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18806755 1323187 Dapk1 death associated protein kinase 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 1323187 Dapk1 death associated protein kinase 1 gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20141836 1323187 Dapk1 death associated protein kinase 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18806755 1323187 Dapk1 death associated protein kinase 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20141836 1323187 Dapk1 death associated protein kinase 1 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:20141836 1323187 Dapk1 death associated protein kinase 1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:20141836 1323187 Dapk1 death associated protein kinase 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:18806755 1323187 Dapk1 death associated protein kinase 1 gene MP:0011372 decreased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15010850 1323187 Dapk1 death associated protein kinase 1 gene MP:0011372 decreased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18806755 1323194 Slc7a13 solute carrier family 7, (cationic amino acid transporter, y+ system) member 13 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20160811 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20160811 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20160811 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0000897 abnormal midbrain morphology IEA N RGD:5509061 20160811 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220519 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20160811 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20160811 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20160811 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20160421 MGI 1323195 Anapc15 anaphase promoting complex C subunit 15 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20160811 MGI 1323199 Kmt5b lysine methyltransferase 5B gene MP:0001258 decreased body length IEA N RGD:5509061 20141003 MGI 1323199 Kmt5b lysine methyltransferase 5B gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1323199 Kmt5b lysine methyltransferase 5B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18676810 1323199 Kmt5b lysine methyltransferase 5B gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20160804 MGI 1323199 Kmt5b lysine methyltransferase 5B gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:18676810 1323199 Kmt5b lysine methyltransferase 5B gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18676810 1323199 Kmt5b lysine methyltransferase 5B gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1323199 Kmt5b lysine methyltransferase 5B gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18676810 1323199 Kmt5b lysine methyltransferase 5B gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20160804 MGI 1323199 Kmt5b lysine methyltransferase 5B gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:18676810 1323199 Kmt5b lysine methyltransferase 5B gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18676810 1323199 Kmt5b lysine methyltransferase 5B gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18676810 1323199 Kmt5b lysine methyltransferase 5B gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:18676810 1323199 Kmt5b lysine methyltransferase 5B gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:18676810 1323199 Kmt5b lysine methyltransferase 5B gene MP:0008409 increased cellular sensitivity to hydroxyurea IAGP N RGD:5509061 20141003 MGI PMID:18676810 1323199 Kmt5b lysine methyltransferase 5B gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:18676810 1323199 Kmt5b lysine methyltransferase 5B gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20141003 MGI 1323199 Kmt5b lysine methyltransferase 5B gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20160804 MGI 1323199 Kmt5b lysine methyltransferase 5B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18676810 1323199 Kmt5b lysine methyltransferase 5B gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18676810 1323199 Kmt5b lysine methyltransferase 5B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1323199 Kmt5b lysine methyltransferase 5B gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:18676810 1323204 Cep290 centrosomal protein 290 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20200310 MGI PMID:24946806 1323204 Cep290 centrosomal protein 290 gene MP:0000542 left-sided isomerism IEA N RGD:5509061 20141003 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20141003 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:21623382 1323204 Cep290 centrosomal protein 290 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:21623382 1323204 Cep290 centrosomal protein 290 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:21245082 1323204 Cep290 centrosomal protein 290 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21623382 1323204 Cep290 centrosomal protein 290 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:16632484 1323204 Cep290 centrosomal protein 290 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:21623382 1323204 Cep290 centrosomal protein 290 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0001426 polydipsia IAGP N RGD:5509061 20160304 MGI PMID:24946806 1323204 Cep290 centrosomal protein 290 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20230601 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0001762 polyuria IAGP N RGD:5509061 20160304 MGI PMID:24946806 1323204 Cep290 centrosomal protein 290 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20160304 MGI PMID:24946806 1323204 Cep290 centrosomal protein 290 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0001925 male infertility IEA N RGD:5509061 20111124 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0001926 female infertility IEA N RGD:5509061 20111124 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24223178 1323204 Cep290 centrosomal protein 290 gene MP:0002639 micrognathia IEA N RGD:5509061 20141003 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20160519 MGI PMID:26301811 1323204 Cep290 centrosomal protein 290 gene MP:0003342 accessory spleen IEA N RGD:5509061 20141003 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20160304 MGI PMID:24946806 1323204 Cep290 centrosomal protein 290 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21245082 1323204 Cep290 centrosomal protein 290 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20210128 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16632484 1323204 Cep290 centrosomal protein 290 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16632484 1323204 Cep290 centrosomal protein 290 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21245082 1323204 Cep290 centrosomal protein 290 gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0004512 anosmia IAGP N RGD:5509061 20141003 MGI PMID:17898177 1323204 Cep290 centrosomal protein 290 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20160304 MGI PMID:24946806 1323204 Cep290 centrosomal protein 290 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20150416 MGI PMID:16632484 1323204 Cep290 centrosomal protein 290 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20141003 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20160519 MGI PMID:26301811 1323204 Cep290 centrosomal protein 290 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21245082 1323204 Cep290 centrosomal protein 290 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21245082 1323204 Cep290 centrosomal protein 290 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200206 MGI PMID:29899041 1323204 Cep290 centrosomal protein 290 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21245082 1323204 Cep290 centrosomal protein 290 gene MP:0008489 slow postnatal weight gain IEA N RGD:5509061 20111124 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:16632484 1323204 Cep290 centrosomal protein 290 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21245082 1323204 Cep290 centrosomal protein 290 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20160304 MGI PMID:24946806 1323204 Cep290 centrosomal protein 290 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20160304 MGI PMID:24946806 1323204 Cep290 centrosomal protein 290 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20141003 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20160304 MGI PMID:24946806 1323204 Cep290 centrosomal protein 290 gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:21245082 1323204 Cep290 centrosomal protein 290 gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20160304 MGI PMID:24946806 1323204 Cep290 centrosomal protein 290 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:16632484 1323204 Cep290 centrosomal protein 290 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:21245082 1323204 Cep290 centrosomal protein 290 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20160304 MGI PMID:24946806 1323204 Cep290 centrosomal protein 290 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:21245082 1323204 Cep290 centrosomal protein 290 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17898177 1323204 Cep290 centrosomal protein 290 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:21623382 1323204 Cep290 centrosomal protein 290 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141003 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0010403 atrial septal defect IEA N RGD:5509061 20141003 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0010419 inlet ventricular septal defect IEA N RGD:5509061 20141003 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20160519 MGI PMID:26301811 1323204 Cep290 centrosomal protein 290 gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20160304 MGI PMID:24946806 1323204 Cep290 centrosomal protein 290 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20160304 MGI PMID:24946806 1323204 Cep290 centrosomal protein 290 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20210128 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0011665 d-loop transposition of the great arteries IEA N RGD:5509061 20141003 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0011682 renal glomerulus cyst IEA N RGD:5509061 20141003 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20141003 MGI 1323204 Cep290 centrosomal protein 290 gene MP:0012671 retina spots IAGP N RGD:5509061 20150416 MGI PMID:16632484 1323204 Cep290 centrosomal protein 290 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:24051377 1323204 Cep290 centrosomal protein 290 gene MP:0020384 absent kidney epithelial cell primary cilium IAGP N RGD:5509061 20161013 MGI PMID:26301811 1323204 Cep290 centrosomal protein 290 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:24946806 1323207 Dbndd2 dysbindin domain containing 2 gene MP:0001147 small testis IEA N RGD:5509061 20160811 MGI 1323207 Dbndd2 dysbindin domain containing 2 gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 1323207 Dbndd2 dysbindin domain containing 2 gene MP:0004930 small epididymis IEA N RGD:5509061 20160811 MGI 1323207 Dbndd2 dysbindin domain containing 2 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20211021 MGI 1323207 Dbndd2 dysbindin domain containing 2 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1323207 Dbndd2 dysbindin domain containing 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1323207 Dbndd2 dysbindin domain containing 2 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20160811 MGI 1323213 Sart3 squamous cell carcinoma antigen recognized by T cells 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 1323213 Sart3 squamous cell carcinoma antigen recognized by T cells 3 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241010 MGI 1323213 Sart3 squamous cell carcinoma antigen recognized by T cells 3 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21447833 1323213 Sart3 squamous cell carcinoma antigen recognized by T cells 3 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1323213 Sart3 squamous cell carcinoma antigen recognized by T cells 3 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21447833 1323213 Sart3 squamous cell carcinoma antigen recognized by T cells 3 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21447833 1323213 Sart3 squamous cell carcinoma antigen recognized by T cells 3 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21447833 1323213 Sart3 squamous cell carcinoma antigen recognized by T cells 3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1323213 Sart3 squamous cell carcinoma antigen recognized by T cells 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1323216 Ldah lipid droplet associated hydrolase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1323216 Ldah lipid droplet associated hydrolase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:27836991 1323216 Ldah lipid droplet associated hydrolase gene MP:0003212 increased susceptibility to age related obesity IEA N RGD:5509061 20161103 MGI 1323216 Ldah lipid droplet associated hydrolase gene MP:0006325 impaired hearing IEA N RGD:5509061 20161103 MGI 1323216 Ldah lipid droplet associated hydrolase gene MP:0009219 increased prostate intraepithelial neoplasia incidence IEA N RGD:5509061 20161103 MGI 1323218 Stat2 signal transducer and activator of transcription 2 gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:19272190 1323218 Stat2 signal transducer and activator of transcription 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11163195 1323218 Stat2 signal transducer and activator of transcription 2 gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:19272190 1323218 Stat2 signal transducer and activator of transcription 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1323218 Stat2 signal transducer and activator of transcription 2 gene MP:0008083 decreased single-positive T cell number IEA N RGD:5509061 20181011 MGI 1323218 Stat2 signal transducer and activator of transcription 2 gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:19272190 1323218 Stat2 signal transducer and activator of transcription 2 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:19272190 1323218 Stat2 signal transducer and activator of transcription 2 gene MP:0010848 decreased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1323218 Stat2 signal transducer and activator of transcription 2 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:11163195 1323218 Stat2 signal transducer and activator of transcription 2 gene MP:0020943 increased susceptibility to Flaviviridae infection IAGP N RGD:5509061 20200430 MGI PMID:29746837 1323218 Stat2 signal transducer and activator of transcription 2 gene MP:0031040 increased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:19272190 1323218 Stat2 signal transducer and activator of transcription 2 gene MP:0031044 increased susceptibility to Flaviviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:29746837 1323224 Vgll4 vestigial like family member 4 gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210520 MGI 1323224 Vgll4 vestigial like family member 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20240523 MGI 1323224 Vgll4 vestigial like family member 4 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0010605 thick pulmonary valve cusps IAGP N RGD:5509061 20191010 MGI PMID:30789911 1323224 Vgll4 vestigial like family member 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323224 Vgll4 vestigial like family member 4 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 1323225 Lrrc56 leucine rich repeat containing 56 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1323225 Lrrc56 leucine rich repeat containing 56 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20220519 MGI 1323225 Lrrc56 leucine rich repeat containing 56 gene MP:0001258 decreased body length IEA N RGD:5509061 20210520 MGI 1323225 Lrrc56 leucine rich repeat containing 56 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1323225 Lrrc56 leucine rich repeat containing 56 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1323225 Lrrc56 leucine rich repeat containing 56 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1323225 Lrrc56 leucine rich repeat containing 56 gene MP:0004085 abnormal heartbeat IEA N RGD:5509061 20220519 MGI 1323225 Lrrc56 leucine rich repeat containing 56 gene MP:0006065 abnormal heart position or orientation IEA N RGD:5509061 20220519 MGI 1323227 Arl15 ADP-ribosylation factor-like 15 gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 1323227 Arl15 ADP-ribosylation factor-like 15 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20221215 MGI 1323227 Arl15 ADP-ribosylation factor-like 15 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323229 Best1 bestrophin 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20191212 MGI PMID:31201163 1323229 Best1 bestrophin 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20160602 MGI PMID:25941382 1323229 Best1 bestrophin 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20160602 MGI PMID:25941382 1323229 Best1 bestrophin 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20160602 MGI PMID:25941382 1323229 Best1 bestrophin 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20191212 MGI PMID:31201163 1323229 Best1 bestrophin 1 gene MP:0003099 retina detachment IAGP N RGD:5509061 20141003 MGI PMID:20053664 1323229 Best1 bestrophin 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20160602 MGI PMID:25941382 1323229 Best1 bestrophin 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20053664 1323229 Best1 bestrophin 1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:16636205 1323229 Best1 bestrophin 1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:20053664 1323229 Best1 bestrophin 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16636205 1323229 Best1 bestrophin 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20053664 1323229 Best1 bestrophin 1 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20160602 MGI PMID:25941382 1323229 Best1 bestrophin 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20160602 MGI PMID:25941382 1323229 Best1 bestrophin 1 gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20160602 MGI PMID:25941382 1323229 Best1 bestrophin 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20160602 MGI PMID:25941382 1323229 Best1 bestrophin 1 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20160602 MGI PMID:25941382 1323229 Best1 bestrophin 1 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20160602 MGI PMID:25941382 1323229 Best1 bestrophin 1 gene MP:0009325 necrospermia IAGP N RGD:5509061 20160602 MGI PMID:25941382 1323232 Pdcd1 programmed cell death 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11209085 1323232 Pdcd1 programmed cell death 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11209085 1323232 Pdcd1 programmed cell death 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22949674 1323232 Pdcd1 programmed cell death 1 gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22432050 1323232 Pdcd1 programmed cell death 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:11209085 1323232 Pdcd1 programmed cell death 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9796923 1323232 Pdcd1 programmed cell death 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20161013 MGI PMID:27410049 1323232 Pdcd1 programmed cell death 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20200618 MGI PMID:27410049 1323232 Pdcd1 programmed cell death 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20161013 MGI PMID:27410049 1323232 Pdcd1 programmed cell death 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22432050 1323232 Pdcd1 programmed cell death 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11209085 1323232 Pdcd1 programmed cell death 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9796923 1323232 Pdcd1 programmed cell death 1 gene MP:0001627 abnormal cardiac output IAGP N RGD:5509061 20141003 MGI PMID:11209085 1323232 Pdcd1 programmed cell death 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20160602 MGI PMID:25964334 1323232 Pdcd1 programmed cell death 1 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:22949674 1323232 Pdcd1 programmed cell death 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20160602 MGI PMID:25964334 1323232 Pdcd1 programmed cell death 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20160602 MGI PMID:25964334 1323232 Pdcd1 programmed cell death 1 gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20141003 MGI PMID:17911591 1323232 Pdcd1 programmed cell death 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:17911591 1323232 Pdcd1 programmed cell death 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20161013 MGI PMID:27410049 1323232 Pdcd1 programmed cell death 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11209085 1323232 Pdcd1 programmed cell death 1 gene MP:0002083 premature death IAGP N RGD:5509061 20161013 MGI PMID:27410049 1323232 Pdcd1 programmed cell death 1 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9796923 1323232 Pdcd1 programmed cell death 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20160602 MGI PMID:25964334 1323232 Pdcd1 programmed cell death 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:9796923 1323232 Pdcd1 programmed cell death 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20160602 MGI PMID:25964334 1323232 Pdcd1 programmed cell death 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:10485649 1323232 Pdcd1 programmed cell death 1 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:11209085 1323232 Pdcd1 programmed cell death 1 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11209085 1323232 Pdcd1 programmed cell death 1 gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:19420345 1323232 Pdcd1 programmed cell death 1 gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:10485649 1323232 Pdcd1 programmed cell death 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17182110 1323232 Pdcd1 programmed cell death 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11209085 1323232 Pdcd1 programmed cell death 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22949674 1323232 Pdcd1 programmed cell death 1 gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:22432050 1323232 Pdcd1 programmed cell death 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:11209085 1323232 Pdcd1 programmed cell death 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:22432050 1323232 Pdcd1 programmed cell death 1 gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:17911591 1323232 Pdcd1 programmed cell death 1 gene MP:0004752 decreased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:16237069 1323232 Pdcd1 programmed cell death 1 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:17182110 1323232 Pdcd1 programmed cell death 1 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20160602 MGI PMID:25964334 1323232 Pdcd1 programmed cell death 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:18832734 1323232 Pdcd1 programmed cell death 1 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:17911591 1323232 Pdcd1 programmed cell death 1 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:17911591 1323232 Pdcd1 programmed cell death 1 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22949674 1323232 Pdcd1 programmed cell death 1 gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:9796923 1323232 Pdcd1 programmed cell death 1 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:17911591 1323232 Pdcd1 programmed cell death 1 gene MP:0005000 abnormal immune tolerance IAGP N RGD:5509061 20141003 MGI PMID:17911591 1323232 Pdcd1 programmed cell death 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9796923 1323232 Pdcd1 programmed cell death 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9796923 1323232 Pdcd1 programmed cell death 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17911591 1323232 Pdcd1 programmed cell death 1 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9796923 1323232 Pdcd1 programmed cell death 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16237069 1323232 Pdcd1 programmed cell death 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17911591 1323232 Pdcd1 programmed cell death 1 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20161013 MGI PMID:27410049 1323232 Pdcd1 programmed cell death 1 gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9796923 1323232 Pdcd1 programmed cell death 1 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:16237069 1323232 Pdcd1 programmed cell death 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22949674 1323232 Pdcd1 programmed cell death 1 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:11209085 1323232 Pdcd1 programmed cell death 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17182110 1323232 Pdcd1 programmed cell death 1 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:22949674 1323232 Pdcd1 programmed cell death 1 gene MP:0008091 decreased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:22949674 1323232 Pdcd1 programmed cell death 1 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20200618 MGI PMID:27410049 1323232 Pdcd1 programmed cell death 1 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:9796923 1323232 Pdcd1 programmed cell death 1 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9796923 1323232 Pdcd1 programmed cell death 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22949674 1323232 Pdcd1 programmed cell death 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20160602 MGI PMID:25964334 1323232 Pdcd1 programmed cell death 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22949674 1323232 Pdcd1 programmed cell death 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20160602 MGI PMID:25964334 1323232 Pdcd1 programmed cell death 1 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20160602 MGI PMID:25964334 1323232 Pdcd1 programmed cell death 1 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:22949674 1323232 Pdcd1 programmed cell death 1 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:22949674 1323232 Pdcd1 programmed cell death 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:22432050 1323232 Pdcd1 programmed cell death 1 gene MP:0009148 pancreas necrosis IAGP N RGD:5509061 20160602 MGI PMID:25964334 1323232 Pdcd1 programmed cell death 1 gene MP:0009646 urinary bladder inflammation IAGP N RGD:5509061 20141003 MGI PMID:22432050 1323232 Pdcd1 programmed cell death 1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22949674 1323232 Pdcd1 programmed cell death 1 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22949674 1323232 Pdcd1 programmed cell death 1 gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:22949674 1323232 Pdcd1 programmed cell death 1 gene MP:0010857 pulmonary necrosis IAGP N RGD:5509061 20160602 MGI PMID:25964334 1323232 Pdcd1 programmed cell death 1 gene MP:0011887 decreased circulating lipase level IAGP N RGD:5509061 20161013 MGI PMID:27410049 1323232 Pdcd1 programmed cell death 1 gene MP:0013295 pancreas atrophy IAGP N RGD:5509061 20161013 MGI PMID:27410049 1323232 Pdcd1 programmed cell death 1 gene MP:0013772 increased effector memory T-helper cell number IAGP N RGD:5509061 20161013 MGI PMID:27410049 1323232 Pdcd1 programmed cell death 1 gene MP:0020993 abnormal urine cytokine level IAGP N RGD:5509061 20210408 MGI PMID:22432050 1323232 Pdcd1 programmed cell death 1 gene MP:0021160 decreased heart right ventricle wall thickness IAGP N RGD:5509061 20231221 MGI PMID:11209085 1323235 Get4 golgi to ER traffic protein 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323235 Get4 golgi to ER traffic protein 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20190606 MGI PMID:30532139 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:21548880 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21548880 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:21548880 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20190606 MGI PMID:30532139 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:23141541 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23141541 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20190606 MGI PMID:30532139 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20190606 MGI PMID:30532139 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21548880 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20190606 MGI PMID:30532139 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0004203 abnormal cranial flexure morphology IAGP N RGD:5509061 20190606 MGI PMID:30532139 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:23141541 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20190606 MGI PMID:30532139 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:23141541 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20190606 MGI PMID:30532139 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20190606 MGI PMID:30532139 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:23141541 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20190606 MGI PMID:30532139 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20190606 MGI PMID:30532139 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23141541 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21548880 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20190606 MGI PMID:30532139 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:23141541 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:30532139 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1323236 Ttbk2 tau tubulin kinase 2 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20210826 MGI 1323238 Fam3b FAM3 metabolism regulating signaling molecule B gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20566664 1323238 Fam3b FAM3 metabolism regulating signaling molecule B gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20566664 1323238 Fam3b FAM3 metabolism regulating signaling molecule B gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20566664 1323238 Fam3b FAM3 metabolism regulating signaling molecule B gene MP:0003839 abnormal insulin clearance IAGP N RGD:5509061 20141003 MGI PMID:20566664 1323238 Fam3b FAM3 metabolism regulating signaling molecule B gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20566664 1323242 Ankrd50 ankyrin repeat domain 50 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1323242 Ankrd50 ankyrin repeat domain 50 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230601 MGI 1323242 Ankrd50 ankyrin repeat domain 50 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1323245 Nkapl NFKB activating protein-like gene MP:0001147 small testis IAGP N RGD:5509061 20160512 MGI PMID:25875095 1323245 Nkapl NFKB activating protein-like gene MP:0001925 male infertility IAGP N RGD:5509061 20160512 MGI PMID:25875095 1323245 Nkapl NFKB activating protein-like gene MP:0005159 azoospermia IAGP N RGD:5509061 20160512 MGI PMID:25875095 1323245 Nkapl NFKB activating protein-like gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20160512 MGI PMID:25875095 1323245 Nkapl NFKB activating protein-like gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20160512 MGI PMID:25875095 1323247 F13b coagulation factor XIII, beta subunit gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20150827 MGI PMID:18224415 1323249 Thoc3 THO complex 3 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20240926 MGI 1323249 Thoc3 THO complex 3 gene MP:0002718 abnormal inner cell mass morphology IEA N RGD:5509061 20240926 MGI 1323249 Thoc3 THO complex 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220519 MGI 1323249 Thoc3 THO complex 3 gene MP:0005028 abnormal trophectoderm morphology IEA N RGD:5509061 20240926 MGI 1323249 Thoc3 THO complex 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1323249 Thoc3 THO complex 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1323249 Thoc3 THO complex 3 gene MP:0012111 failure of morula compaction IEA N RGD:5509061 20240926 MGI 1323249 Thoc3 THO complex 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1323249 Thoc3 THO complex 3 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240926 MGI 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20171005 MGI PMID:19718027 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20171005 MGI PMID:19718027 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:22393260 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22573616 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:22007134 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0001199 thin skin IAGP N RGD:5509061 20171005 MGI PMID:19718027 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0001218 thin epidermis IAGP N RGD:5509061 20171005 MGI PMID:19718027 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20171005 MGI PMID:19718027 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20171005 MGI PMID:19718027 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:22007134 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:22007134 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:22573616 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0001314 cornea opacity IEA N RGD:5509061 20160804 MGI 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:22573616 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22573616 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:22393260 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150430 MGI PMID:25038042 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20171005 MGI PMID:19718027 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:22573616 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:22573616 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20171005 MGI PMID:19718027 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:22573616 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:22573616 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:22573616 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20171005 MGI PMID:19718027 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20141003 MGI PMID:22573616 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22573616 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22573616 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:22007134 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0012156 rostral-caudal axis duplication IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0012181 increased somite number IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0012274 increased axial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:14668413 1323252 Tcf7l1 transcription factor 7 like 1 (T cell specific, HMG box) gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:22573616 1323256 Pilrb1 paired immunoglobin-like type 2 receptor beta 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20065029 1323256 Pilrb1 paired immunoglobin-like type 2 receptor beta 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20065029 1323256 Pilrb1 paired immunoglobin-like type 2 receptor beta 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:20065029 1323256 Pilrb1 paired immunoglobin-like type 2 receptor beta 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20065029 1323256 Pilrb1 paired immunoglobin-like type 2 receptor beta 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20065029 1323256 Pilrb1 paired immunoglobin-like type 2 receptor beta 1 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:20065029 1323256 Pilrb1 paired immunoglobin-like type 2 receptor beta 1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20065029 1323256 Pilrb1 paired immunoglobin-like type 2 receptor beta 1 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:20065029 1323256 Pilrb1 paired immunoglobin-like type 2 receptor beta 1 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:20065029 1323256 Pilrb1 paired immunoglobin-like type 2 receptor beta 1 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20065029 1323256 Pilrb1 paired immunoglobin-like type 2 receptor beta 1 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:20065029 1323256 Pilrb1 paired immunoglobin-like type 2 receptor beta 1 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:20065029 1323256 Pilrb1 paired immunoglobin-like type 2 receptor beta 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:20065029 1323256 Pilrb1 paired immunoglobin-like type 2 receptor beta 1 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:20065029 1323256 Pilrb1 paired immunoglobin-like type 2 receptor beta 1 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20065029 1323257 G0s2 G0/G1 switch gene 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160714 MGI PMID:24583640 1323257 G0s2 G0/G1 switch gene 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160623 MGI PMID:24556704 1323257 G0s2 G0/G1 switch gene 2 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20160623 MGI PMID:24556704 1323257 G0s2 G0/G1 switch gene 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20160623 MGI PMID:24556704 1323257 G0s2 G0/G1 switch gene 2 gene MP:0003718 maternal effect IAGP N RGD:5509061 20160623 MGI PMID:24556704 1323257 G0s2 G0/G1 switch gene 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20160623 MGI PMID:24556704 1323257 G0s2 G0/G1 switch gene 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20160623 MGI PMID:24556704 1323257 G0s2 G0/G1 switch gene 2 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20160623 MGI PMID:24556704 1323257 G0s2 G0/G1 switch gene 2 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20160714 MGI PMID:24583640 1323257 G0s2 G0/G1 switch gene 2 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20160623 MGI PMID:24556704 1323257 G0s2 G0/G1 switch gene 2 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20160714 MGI PMID:24583640 1323257 G0s2 G0/G1 switch gene 2 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0009303 decreased renal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20160623 MGI PMID:24556704 1323257 G0s2 G0/G1 switch gene 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20160714 MGI PMID:24583640 1323257 G0s2 G0/G1 switch gene 2 gene MP:0010046 decreased omental fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20160714 MGI PMID:24583640 1323257 G0s2 G0/G1 switch gene 2 gene MP:0011581 increased triglyceride lipase activity IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20160728 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20180125 MGI PMID:24556704 1323257 G0s2 G0/G1 switch gene 2 gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20180125 MGI PMID:25381555 1323257 G0s2 G0/G1 switch gene 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:24194501 1323257 G0s2 G0/G1 switch gene 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:25381555 1323260 Rfx5 regulatory factor X, 5 (influences HLA class II expression) gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9491996 1323260 Rfx5 regulatory factor X, 5 (influences HLA class II expression) gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9491996 1323260 Rfx5 regulatory factor X, 5 (influences HLA class II expression) gene MP:0002453 abnormal B lymphocyte antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:9491996 1323260 Rfx5 regulatory factor X, 5 (influences HLA class II expression) gene MP:0005040 abnormal MHC II cell surface expression on macrophages IAGP N RGD:5509061 20141003 MGI PMID:10621974 1323260 Rfx5 regulatory factor X, 5 (influences HLA class II expression) gene MP:0005040 abnormal MHC II cell surface expression on macrophages IAGP N RGD:5509061 20141003 MGI PMID:9491996 1323260 Rfx5 regulatory factor X, 5 (influences HLA class II expression) gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:9491996 1323260 Rfx5 regulatory factor X, 5 (influences HLA class II expression) gene MP:0005461 abnormal dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9491996 1323260 Rfx5 regulatory factor X, 5 (influences HLA class II expression) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9491996 1323260 Rfx5 regulatory factor X, 5 (influences HLA class II expression) gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9491996 1323260 Rfx5 regulatory factor X, 5 (influences HLA class II expression) gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9491996 1323260 Rfx5 regulatory factor X, 5 (influences HLA class II expression) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9491996 1323265 Tifab TRAF-interacting protein with forkhead-associated domain, family member B gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1323265 Tifab TRAF-interacting protein with forkhead-associated domain, family member B gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20171102 MGI PMID:26458771 1323265 Tifab TRAF-interacting protein with forkhead-associated domain, family member B gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20171102 MGI PMID:26458771 1323265 Tifab TRAF-interacting protein with forkhead-associated domain, family member B gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20171102 MGI PMID:26458771 1323265 Tifab TRAF-interacting protein with forkhead-associated domain, family member B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20171102 MGI PMID:26458771 1323265 Tifab TRAF-interacting protein with forkhead-associated domain, family member B gene MP:0002083 premature death IAGP N RGD:5509061 20171102 MGI PMID:26458771 1323265 Tifab TRAF-interacting protein with forkhead-associated domain, family member B gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220811 MGI 1323265 Tifab TRAF-interacting protein with forkhead-associated domain, family member B gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20171102 MGI PMID:26458771 1323265 Tifab TRAF-interacting protein with forkhead-associated domain, family member B gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20171102 MGI PMID:26458771 1323265 Tifab TRAF-interacting protein with forkhead-associated domain, family member B gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20171102 MGI PMID:26458771 1323265 Tifab TRAF-interacting protein with forkhead-associated domain, family member B gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20171102 MGI PMID:26458771 1323265 Tifab TRAF-interacting protein with forkhead-associated domain, family member B gene MP:0011903 decreased hematopoietic stem cell proliferation IAGP N RGD:5509061 20171102 MGI PMID:26458771 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20160804 MGI 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20160804 MGI 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20160922 MGI PMID:24652767 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160407 MGI PMID:24923387 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160922 MGI PMID:24652767 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160407 MGI PMID:24923387 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20160922 MGI PMID:24652767 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20160407 MGI PMID:24923387 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20160407 MGI PMID:24923387 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20160407 MGI PMID:24923387 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20160407 MGI PMID:24923387 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0005353 abnormal patella morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20160922 MGI PMID:24652767 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160922 MGI PMID:24652767 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160804 MGI 1323268 Rhobtb3 Rho-related BTB domain containing 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20160407 MGI PMID:24923387 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0001438 aphagia IAGP N RGD:5509061 20141106 MGI PMID:24487590 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0001460 abnormal olfactory discrimination memory IAGP N RGD:5509061 20141106 MGI PMID:24487590 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141106 MGI PMID:24487590 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141106 MGI PMID:24487590 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141106 MGI PMID:24487590 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0003110 absent malleus processus brevis IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141106 MGI PMID:24487590 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0006033 abnormal external auditory canal morphology IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0008377 absent malleus manubrium IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0008382 gonial bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0009879 abnormal arcus anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0009943 abnormal olfactory bulb periglomerular cell morphology IAGP N RGD:5509061 20141106 MGI PMID:24487590 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0009949 abnormal olfactory bulb granule cell layer morphology IAGP N RGD:5509061 20141106 MGI PMID:24487590 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0010371 abnormal epiglottis morphology IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0010994 aerophagia IAGP N RGD:5509061 20141106 MGI PMID:24487590 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141106 MGI PMID:24487590 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141106 MGI PMID:24487590 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0012284 increased sternebra number IAGP N RGD:5509061 20141003 MGI PMID:17586487 1323270 Tshz1 teashirt zinc finger family member 1 gene MP:0030291 short soft palate IAGP N RGD:5509061 20171102 MGI PMID:17586487 1323272 Nid2 nidogen 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20160811 MGI PMID:26683663 1323272 Nid2 nidogen 2 gene MP:0003200 calcified joint IAGP N RGD:5509061 20160811 MGI PMID:26683663 1323272 Nid2 nidogen 2 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20160811 MGI PMID:26683663 1323272 Nid2 nidogen 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17008882 1323272 Nid2 nidogen 2 gene MP:0006429 abnormal hyaline cartilage morphology IAGP N RGD:5509061 20160811 MGI PMID:26683663 1323274 Bpifc BPI fold containing family C gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20220811 MGI 1323274 Bpifc BPI fold containing family C gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1323274 Bpifc BPI fold containing family C gene MP:0005655 increased aggression IEA N RGD:5509061 20221215 MGI 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20231207 MGI 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:19365570 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:19365570 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20220811 MGI 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20220519 MGI 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19365570 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0004222 iris synechia IAGP N RGD:5509061 20141003 MGI PMID:19365570 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0005195 abnormal posterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:19365570 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:19365570 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:19365570 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20141003 MGI PMID:19365570 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:19365570 1323277 Bcar3 breast cancer anti-estrogen resistance 3 gene MP:0031213 increased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:19365570 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0000410 waved hair IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20190808 MGI 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0000692 small spleen IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0000706 small thymus IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20210520 MGI 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0001399 hyperactivity IAGP N RGD:5509061 20201029 MGI PMID:28436964 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190808 MGI 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0001924 infertility IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0002083 premature death IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0004882 enlarged lung IEA N RGD:5509061 20210520 MGI 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20201029 MGI PMID:28436964 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0004917 abnormal T cell selection IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20201029 MGI PMID:28436964 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0005331 insulin resistance IAGP N RGD:5509061 20201029 MGI PMID:28436964 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20201029 MGI PMID:28436964 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20201029 MGI PMID:28436964 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20201029 MGI PMID:28436964 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20201029 MGI PMID:28436964 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0009434 paraparesis IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20201029 MGI PMID:28436964 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0010132 decreased DN2 thymocyte number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0010134 decreased DN3 thymocyte number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0013592 small thymus cortex IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0013741 absent thymus corticomedullary boundary IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323280 Lrrc8a leucine rich repeat containing 8A VRAC subunit A gene MP:0014180 abnormal thymus apoptosis IAGP N RGD:5509061 20170314 MGI PMID:24752297 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221201 MGI PMID:25430793 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20221201 MGI PMID:25430793 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20221201 MGI PMID:25430793 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0001241 absent epidermis stratum corneum IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20221201 MGI PMID:25430793 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20221201 MGI PMID:25430793 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0003130 anal atresia IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0003276 esophageal atresia IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0003276 esophageal atresia IAGP N RGD:5509061 20221201 MGI PMID:25430793 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0009576 oral atresia IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0009576 oral atresia IAGP N RGD:5509061 20221201 MGI PMID:25430793 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221201 MGI PMID:25430793 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0009884 palatal shelf fusion with tongue or mandible IAGP N RGD:5509061 20221201 MGI PMID:25430793 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221201 MGI PMID:25430793 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20170309 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0011771 abnormal genital tubercle morphology IAGP N RGD:5509061 20221201 MGI PMID:25430793 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0013530 abnormal periderm morphology IAGP N RGD:5509061 20221201 MGI PMID:25430793 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0013531 abnormal periderm development IAGP N RGD:5509061 20221201 MGI PMID:25430793 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:12194825 1323282 Ripk4 receptor-interacting serine-threonine kinase 4 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20221201 MGI PMID:25430793 1323293 Dpf2 double PHD fingers 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1323293 Dpf2 double PHD fingers 2 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20181227 MGI 1323293 Dpf2 double PHD fingers 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20170105 MGI 1323293 Dpf2 double PHD fingers 2 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1323293 Dpf2 double PHD fingers 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20160811 MGI 1323293 Dpf2 double PHD fingers 2 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20201231 MGI 1323293 Dpf2 double PHD fingers 2 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20201231 MGI 1323293 Dpf2 double PHD fingers 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20160811 MGI 1323293 Dpf2 double PHD fingers 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1323293 Dpf2 double PHD fingers 2 gene MP:0003717 pallor IEA N RGD:5509061 20201231 MGI 1323293 Dpf2 double PHD fingers 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1323295 Smtnl1 smoothelin-like 1 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:18310078 1323295 Smtnl1 smoothelin-like 1 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:18310078 1323295 Smtnl1 smoothelin-like 1 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:18310078 1323295 Smtnl1 smoothelin-like 1 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:18310078 1323295 Smtnl1 smoothelin-like 1 gene MP:0012107 enhanced exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:18310078 1323297 Uba5 ubiquitin-like modifier activating enzyme 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20018847 1323303 Hdac11 histone deacetylase 11 gene MP:0001257 increased body length IEA N RGD:5509061 20230601 MGI 1323303 Hdac11 histone deacetylase 11 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1323303 Hdac11 histone deacetylase 11 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20160225 MGI PMID:25155994 1323303 Hdac11 histone deacetylase 11 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20160225 MGI PMID:25155994 1323303 Hdac11 histone deacetylase 11 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20160225 MGI PMID:24747960 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:23209306 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17925231 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23209306 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:17925231 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:23209306 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17925231 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23209306 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17925231 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23209306 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17938250 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17938250 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17925231 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23209306 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:17925231 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17938250 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:17938250 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:23209306 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:17938250 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:23209306 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:17938250 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:17925231 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17925231 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17938250 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:17925231 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17925231 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23209306 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17938250 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:23209306 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20141003 MGI PMID:17925231 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:17938250 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17925231 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17938250 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:19117986 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17938250 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1323305 Bub1 BUB1, mitotic checkpoint serine/threonine kinase gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17938250 1323312 Itga11 integrin alpha 11 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17420280 1323312 Itga11 integrin alpha 11 gene MP:0000745 tremors IEA N RGD:5509061 20201231 MGI 1323312 Itga11 integrin alpha 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17420280 1323312 Itga11 integrin alpha 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17420280 1323312 Itga11 integrin alpha 11 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:17420280 1323312 Itga11 integrin alpha 11 gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:17420280 1323312 Itga11 integrin alpha 11 gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20141003 MGI PMID:17420280 1323312 Itga11 integrin alpha 11 gene MP:0003053 delayed tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:17420280 1323312 Itga11 integrin alpha 11 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:17420280 1323312 Itga11 integrin alpha 11 gene MP:0003668 abnormal periodontal ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:17420280 1323312 Itga11 integrin alpha 11 gene MP:0004830 short incisors IAGP N RGD:5509061 20141003 MGI PMID:17420280 1323312 Itga11 integrin alpha 11 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220519 MGI 1323312 Itga11 integrin alpha 11 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:17420280 1323312 Itga11 integrin alpha 11 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:17420280 1323312 Itga11 integrin alpha 11 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20240523 MGI 1323312 Itga11 integrin alpha 11 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20200514 MGI 1323312 Itga11 integrin alpha 11 gene MP:0030460 enamel pits IAGP N RGD:5509061 20171221 MGI PMID:17420280 1323312 Itga11 integrin alpha 11 gene MP:0030509 increased number of epithelial cell rests of Malassez IAGP N RGD:5509061 20180111 MGI PMID:17420280 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20170105 MGI 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20160811 MGI 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20170105 MGI 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20201022 MGI 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20200402 MGI 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20210826 MGI 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0001454 abnormal cued conditioning behavior IEA N RGD:5509061 20210128 MGI 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0001469 abnormal contextual conditioning behavior IEA N RGD:5509061 20210128 MGI 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20201022 MGI 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20200402 MGI 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20201022 MGI 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160421 MGI 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20170105 MGI 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0011906 increased Schwann cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:16136673 1323314 Nab2 Ngfi-A binding protein 2 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20210128 MGI 1323317 Rsrc2 arginine/serine-rich coiled-coil 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1323320 Ubap2 ubiquitin-associated protein 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1323320 Ubap2 ubiquitin-associated protein 2 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20220519 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:13989207 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0000400 abnormal awl hair morphology IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0000402 abnormal zigzag hair morphology IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0000414 alopecia IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:12533510 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:12748961 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0000422 delayed hair appearance IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0000424 retarded hair growth IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0001270 distended abdomen IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0001282 short vibrissae IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:12748961 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0001575 cyanosis IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19429912 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:12748961 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19429912 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:18931657 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:19429912 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18931657 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19429912 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:11094083 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:12533510 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19429912 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:12748961 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19429912 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201231 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:11094083 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:12533510 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20201022 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:19429912 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0006363 absent auchene hairs IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0008538 decreased zigzag hair amount IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0008817 hematoma IAGP N RGD:5509061 20141003 MGI PMID:19429912 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0009003 abnormal vibrissa number IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20150730 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12748961 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0011088 neonatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0011090 perinatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0011092 embryonic lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18931657 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19429912 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12748961 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0011748 intestinal fibrosis IEA N RGD:5509061 20150730 MGI 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0012080 chylous ascites IAGP N RGD:5509061 20141003 MGI PMID:12748961 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0012080 chylous ascites IAGP N RGD:5509061 20150730 MGI PMID:291594 1323322 Sox18 SRY (sex determining region Y)-box 18 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1323326 Sec24d SEC24 homolog D, COPII coat complex component gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20200514 MGI 1323326 Sec24d SEC24 homolog D, COPII coat complex component gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20200514 MGI 1323326 Sec24d SEC24 homolog D, COPII coat complex component gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170518 MGI PMID:24876386 1323326 Sec24d SEC24 homolog D, COPII coat complex component gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20200514 MGI 1323326 Sec24d SEC24 homolog D, COPII coat complex component gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23596517 1323326 Sec24d SEC24 homolog D, COPII coat complex component gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23596517 1323326 Sec24d SEC24 homolog D, COPII coat complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323328 Nmi N-myc (and STAT) interactor gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200416 MGI PMID:29326438 1323328 Nmi N-myc (and STAT) interactor gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20200416 MGI PMID:29326438 1323328 Nmi N-myc (and STAT) interactor gene MP:0001884 mammary gland alveolar hyperplasia IAGP N RGD:5509061 20200416 MGI PMID:29326438 1323328 Nmi N-myc (and STAT) interactor gene MP:0001885 mammary gland duct hyperplasia IAGP N RGD:5509061 20200416 MGI PMID:29326438 1323328 Nmi N-myc (and STAT) interactor gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20211021 MGI PMID:29038465 1323328 Nmi N-myc (and STAT) interactor gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20200416 MGI PMID:29326438 1323328 Nmi N-myc (and STAT) interactor gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20211021 MGI PMID:29038465 1323328 Nmi N-myc (and STAT) interactor gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20211021 MGI PMID:29038465 1323328 Nmi N-myc (and STAT) interactor gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20211021 MGI PMID:29038465 1323328 Nmi N-myc (and STAT) interactor gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20211021 MGI PMID:29038465 1323328 Nmi N-myc (and STAT) interactor gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20200416 MGI PMID:29326438 1323328 Nmi N-myc (and STAT) interactor gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20211021 MGI PMID:29038465 1323328 Nmi N-myc (and STAT) interactor gene MP:0013782 abnormal mammary duct terminal end bud morphology IAGP N RGD:5509061 20200416 MGI PMID:29326438 1323329 Cep295 centrosomal protein 295 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20240523 MGI 1323329 Cep295 centrosomal protein 295 gene MP:0001925 male infertility IEA N RGD:5509061 20240523 MGI 1323329 Cep295 centrosomal protein 295 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1323331 Capg capping actin protein, gelsolin like gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:11514591 1323331 Capg capping actin protein, gelsolin like gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:14573680 1323331 Capg capping actin protein, gelsolin like gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14573680 1323331 Capg capping actin protein, gelsolin like gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:14573680 1323331 Capg capping actin protein, gelsolin like gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11514591 1323331 Capg capping actin protein, gelsolin like gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:14573680 1323333 Fgd3 FYVE, RhoGEF and PH domain containing 3 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1323333 Fgd3 FYVE, RhoGEF and PH domain containing 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1323333 Fgd3 FYVE, RhoGEF and PH domain containing 3 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1323333 Fgd3 FYVE, RhoGEF and PH domain containing 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1323333 Fgd3 FYVE, RhoGEF and PH domain containing 3 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1323333 Fgd3 FYVE, RhoGEF and PH domain containing 3 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1323333 Fgd3 FYVE, RhoGEF and PH domain containing 3 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220519 MGI 1323335 Gfi1b growth factor independent 1B gene MP:0000215 absent erythrocytes IAGP N RGD:5509061 20141003 MGI PMID:11825872 1323335 Gfi1b growth factor independent 1B gene MP:0000216 absent erythroid progenitor cell IAGP N RGD:5509061 20141003 MGI PMID:24711581 1323335 Gfi1b growth factor independent 1B gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20181227 MGI 1323335 Gfi1b growth factor independent 1B gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:11825872 1323335 Gfi1b growth factor independent 1B gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:24711581 1323335 Gfi1b growth factor independent 1B gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:11825872 1323335 Gfi1b growth factor independent 1B gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:17095621 1323335 Gfi1b growth factor independent 1B gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:24711581 1323335 Gfi1b growth factor independent 1B gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17095621 1323335 Gfi1b growth factor independent 1B gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:11825872 1323335 Gfi1b growth factor independent 1B gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11825872 1323335 Gfi1b growth factor independent 1B gene MP:0002080 prenatal lethality IEA N RGD:5509061 20201231 MGI 1323335 Gfi1b growth factor independent 1B gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:24711581 1323335 Gfi1b growth factor independent 1B gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24711581 1323335 Gfi1b growth factor independent 1B gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20826720 1323335 Gfi1b growth factor independent 1B gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:24711581 1323335 Gfi1b growth factor independent 1B gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20826720 1323335 Gfi1b growth factor independent 1B gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1323335 Gfi1b growth factor independent 1B gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20826720 1323335 Gfi1b growth factor independent 1B gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:24711581 1323335 Gfi1b growth factor independent 1B gene MP:0003714 absent platelets IAGP N RGD:5509061 20141003 MGI PMID:24711581 1323335 Gfi1b growth factor independent 1B gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11825872 1323335 Gfi1b growth factor independent 1B gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:11825872 1323335 Gfi1b growth factor independent 1B gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11825872 1323335 Gfi1b growth factor independent 1B gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20826720 1323335 Gfi1b growth factor independent 1B gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20826720 1323335 Gfi1b growth factor independent 1B gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 1323335 Gfi1b growth factor independent 1B gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1323335 Gfi1b growth factor independent 1B gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:20826720 1323335 Gfi1b growth factor independent 1B gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1323335 Gfi1b growth factor independent 1B gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20826720 1323335 Gfi1b growth factor independent 1B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24711581 1323335 Gfi1b growth factor independent 1B gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11825872 1323335 Gfi1b growth factor independent 1B gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17095621 1323335 Gfi1b growth factor independent 1B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323340 Gstm6 glutathione S-transferase, mu 6 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1323340 Gstm6 glutathione S-transferase, mu 6 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1323340 Gstm6 glutathione S-transferase, mu 6 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1323340 Gstm6 glutathione S-transferase, mu 6 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1323343 Fxr1 FMR1 autosomal homolog 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15128702 1323343 Fxr1 FMR1 autosomal homolog 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:15128702 1323343 Fxr1 FMR1 autosomal homolog 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:15128702 1323343 Fxr1 FMR1 autosomal homolog 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15128702 1323343 Fxr1 FMR1 autosomal homolog 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15128702 1323343 Fxr1 FMR1 autosomal homolog 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:15128702 1323343 Fxr1 FMR1 autosomal homolog 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15128702 1323343 Fxr1 FMR1 autosomal homolog 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15128702 1323343 Fxr1 FMR1 autosomal homolog 1 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:15128702 1323343 Fxr1 FMR1 autosomal homolog 1 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:15128702 1323343 Fxr1 FMR1 autosomal homolog 1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:15128702 1323343 Fxr1 FMR1 autosomal homolog 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:15128702 1323343 Fxr1 FMR1 autosomal homolog 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15128702 1323343 Fxr1 FMR1 autosomal homolog 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24069363 1323343 Fxr1 FMR1 autosomal homolog 1 gene MP:0014273 abnormal skin vasculature morphology IAGP N RGD:5509061 20230810 MGI PMID:15128702 1323346 Arid5b AT-rich interaction domain 5B gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:14651970 1323346 Arid5b AT-rich interaction domain 5B gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0000091 short premaxilla IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20151203 MGI PMID:24276541 1323346 Arid5b AT-rich interaction domain 5B gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0000445 short snout IAGP N RGD:5509061 20171019 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0000767 abnormal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:14651970 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14651970 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001265 decreased body size IAGP N RGD:5509061 20151203 MGI PMID:24276541 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001376 abnormal mating receptivity IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001377 abnormal mating frequency IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001443 poor grooming IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:14651970 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:14651970 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0002764 short tibia IAGP N RGD:5509061 20151203 MGI PMID:24276541 1323346 Arid5b AT-rich interaction domain 5B gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20151203 MGI PMID:24276541 1323346 Arid5b AT-rich interaction domain 5B gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:14651970 1323346 Arid5b AT-rich interaction domain 5B gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:14651970 1323346 Arid5b AT-rich interaction domain 5B gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20151203 MGI PMID:24276541 1323346 Arid5b AT-rich interaction domain 5B gene MP:0008295 abnormal adrenal gland zona reticularis morphology IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:14651970 1323346 Arid5b AT-rich interaction domain 5B gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17962384 1323346 Arid5b AT-rich interaction domain 5B gene MP:0009137 decreased brown fat lipid droplet number IAGP N RGD:5509061 20141003 MGI PMID:14651970 1323346 Arid5b AT-rich interaction domain 5B gene MP:0009396 small endometrial glands IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0009895 decreased palatine bone horizontal plate size IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14651970 1323346 Arid5b AT-rich interaction domain 5B gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:14651970 1323346 Arid5b AT-rich interaction domain 5B gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:14651970 1323346 Arid5b AT-rich interaction domain 5B gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0030189 broad snout IAGP N RGD:5509061 20171019 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0030383 small presphenoid bone IAGP N RGD:5509061 20171207 MGI PMID:17143286 1323346 Arid5b AT-rich interaction domain 5B gene MP:0031286 unilateral cryptorchism IAGP N RGD:5509061 20211014 MGI PMID:11483573 1323346 Arid5b AT-rich interaction domain 5B gene MP:0031287 bilateral cryptorchism IAGP N RGD:5509061 20211014 MGI PMID:11483573 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20181227 MGI 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8977324 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8849728 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12574333 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16713566 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:8849728 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:8849728 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:8977324 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:17574818 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11238890 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16713566 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8849728 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:8849728 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0002403 abnormal pre-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16713566 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11238890 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17574818 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:8849728 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0002491 decreased IgD level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12574333 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:8849728 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:8849728 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20210128 MGI 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17574818 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11238890 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16713566 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17568779 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8977324 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17568779 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17568779 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8849728 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16713566 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17574818 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:17568779 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:17568779 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:17574818 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:17574818 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11238890 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11238890 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:12574333 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:8849728 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:8977324 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:8849728 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:8977324 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:8849728 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:8977324 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:8849728 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:8977324 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:8849728 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:8977324 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008523 absent lymph node germinal center IAGP N RGD:5509061 20141003 MGI PMID:8849728 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17568779 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:17568779 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17568779 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:17568779 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11238890 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17574818 1323348 Pou2af1 POU domain, class 2, associating factor 1 gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:17574818 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0000601 small liver IEA N RGD:5509061 20210128 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20240627 MGI PMID:32285100 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20240627 MGI PMID:32285100 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20240627 MGI PMID:32285100 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20240627 MGI PMID:32285100 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20240627 MGI PMID:32285100 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20210128 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20240627 MGI PMID:32285100 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20190502 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20240627 MGI PMID:32285100 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20240627 MGI PMID:32285100 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0012128 abnormal blastocyst formation IAGP N RGD:5509061 20240627 MGI PMID:32285100 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1323350 Rbbp4 retinoblastoma binding protein 4, chromatin remodeling factor gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20240627 MGI PMID:32285100 1323356 Cd2bp2 CD2 cytoplasmic tail binding protein 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:26082520 1323356 Cd2bp2 CD2 cytoplasmic tail binding protein 2 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20200310 MGI PMID:26082520 1323356 Cd2bp2 CD2 cytoplasmic tail binding protein 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:26082520 1323356 Cd2bp2 CD2 cytoplasmic tail binding protein 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20200310 MGI PMID:26082520 1323356 Cd2bp2 CD2 cytoplasmic tail binding protein 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:26082520 1323356 Cd2bp2 CD2 cytoplasmic tail binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:26082520 1323356 Cd2bp2 CD2 cytoplasmic tail binding protein 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20200310 MGI PMID:26082520 1323356 Cd2bp2 CD2 cytoplasmic tail binding protein 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20200310 MGI PMID:26082520 1323356 Cd2bp2 CD2 cytoplasmic tail binding protein 2 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20200310 MGI PMID:26082520 1323356 Cd2bp2 CD2 cytoplasmic tail binding protein 2 gene MP:0010666 abnormal vitelline vein morphology IAGP N RGD:5509061 20200310 MGI PMID:26082520 1323356 Cd2bp2 CD2 cytoplasmic tail binding protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:26082520 1323356 Cd2bp2 CD2 cytoplasmic tail binding protein 2 gene MP:0011402 renal cast IAGP N RGD:5509061 20200310 MGI PMID:26082520 1323356 Cd2bp2 CD2 cytoplasmic tail binding protein 2 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20200310 MGI PMID:26082520 1323356 Cd2bp2 CD2 cytoplasmic tail binding protein 2 gene MP:0012131 small visceral yolk sac IAGP N RGD:5509061 20200310 MGI PMID:26082520 1323357 Spata24 spermatogenesis associated 24 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20210128 MGI 1323357 Spata24 spermatogenesis associated 24 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1323357 Spata24 spermatogenesis associated 24 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20231207 MGI 1323357 Spata24 spermatogenesis associated 24 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201022 MGI PMID:32588039 1323361 1110059G10Rik RIKEN cDNA 1110059G10 gene gene MP:0003036 vertebral transformation IEA N RGD:5509061 20150430 MGI 1323364 Hpf1 histone PARylation factor 1 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20181227 MGI 1323364 Hpf1 histone PARylation factor 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1323366 Tcerg1 transcription elongation regulator 1 (CA150) gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1323366 Tcerg1 transcription elongation regulator 1 (CA150) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20210128 MGI PMID:32943573 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20210128 MGI PMID:32943573 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0001147 small testis IAGP N RGD:5509061 20210128 MGI PMID:32943573 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0001147 small testis IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20210128 MGI PMID:32943573 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20171102 MGI PMID:25569111 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210128 MGI PMID:32943573 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0001925 male infertility IAGP N RGD:5509061 20210128 MGI PMID:32943573 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0001925 male infertility IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0001926 female infertility IAGP N RGD:5509061 20210128 MGI PMID:32943573 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210128 MGI PMID:32943573 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20171102 MGI PMID:25569111 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20210128 MGI PMID:32943573 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20210128 MGI PMID:32943573 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20171102 MGI PMID:25569111 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0013272 abnormal translation IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0013600 testis degeneration IAGP N RGD:5509061 20210128 MGI PMID:32943573 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323368 Mettl3 methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210422 MGI PMID:28914256 1323369 Mesp1 mesoderm posterior 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20230309 MGI PMID:23872235 1323369 Mesp1 mesoderm posterior 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16996494 1323369 Mesp1 mesoderm posterior 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:16996494 1323369 Mesp1 mesoderm posterior 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:10887078 1323369 Mesp1 mesoderm posterior 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18547789 1323369 Mesp1 mesoderm posterior 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18832392 1323369 Mesp1 mesoderm posterior 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231109 MGI PMID:34050709 1323369 Mesp1 mesoderm posterior 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10393122 1323369 Mesp1 mesoderm posterior 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16554359 1323369 Mesp1 mesoderm posterior 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18547789 1323369 Mesp1 mesoderm posterior 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18832392 1323369 Mesp1 mesoderm posterior 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9739106 1323369 Mesp1 mesoderm posterior 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:10393122 1323369 Mesp1 mesoderm posterior 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:21089073 1323369 Mesp1 mesoderm posterior 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:9739106 1323369 Mesp1 mesoderm posterior 1 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10393122 1323369 Mesp1 mesoderm posterior 1 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16720879 1323369 Mesp1 mesoderm posterior 1 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20160721 MGI PMID:26932671 1323369 Mesp1 mesoderm posterior 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20160218 MGI PMID:24748541 1323369 Mesp1 mesoderm posterior 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:18547789 1323369 Mesp1 mesoderm posterior 1 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:16554359 1323369 Mesp1 mesoderm posterior 1 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20231109 MGI PMID:34050709 1323369 Mesp1 mesoderm posterior 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16554359 1323369 Mesp1 mesoderm posterior 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16554359 1323369 Mesp1 mesoderm posterior 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:18832392 1323369 Mesp1 mesoderm posterior 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:16554359 1323369 Mesp1 mesoderm posterior 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:18547789 1323369 Mesp1 mesoderm posterior 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16720879 1323369 Mesp1 mesoderm posterior 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:9739106 1323369 Mesp1 mesoderm posterior 1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0001068 abnormal mandibular nerve branching IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0001075 abnormal accessory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:16996494 1323369 Mesp1 mesoderm posterior 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10887078 1323369 Mesp1 mesoderm posterior 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:10887078 1323369 Mesp1 mesoderm posterior 1 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:10887078 1323369 Mesp1 mesoderm posterior 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:10393122 1323369 Mesp1 mesoderm posterior 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:10887078 1323369 Mesp1 mesoderm posterior 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10887078 1323369 Mesp1 mesoderm posterior 1 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:10887078 1323369 Mesp1 mesoderm posterior 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:10887078 1323369 Mesp1 mesoderm posterior 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10887078 1323369 Mesp1 mesoderm posterior 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9739106 1323369 Mesp1 mesoderm posterior 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20231109 MGI PMID:34050709 1323369 Mesp1 mesoderm posterior 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10393122 1323369 Mesp1 mesoderm posterior 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9739106 1323369 Mesp1 mesoderm posterior 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16720879 1323369 Mesp1 mesoderm posterior 1 gene MP:0001785 edema IAGP N RGD:5509061 20160218 MGI PMID:24748541 1323369 Mesp1 mesoderm posterior 1 gene MP:0001785 edema IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20160721 MGI PMID:26932671 1323369 Mesp1 mesoderm posterior 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160218 MGI PMID:24748541 1323369 Mesp1 mesoderm posterior 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20231109 MGI PMID:34050709 1323369 Mesp1 mesoderm posterior 1 gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:10887078 1323369 Mesp1 mesoderm posterior 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9739106 1323369 Mesp1 mesoderm posterior 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23184148 1323369 Mesp1 mesoderm posterior 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:34767447 1323369 Mesp1 mesoderm posterior 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:36693621 1323369 Mesp1 mesoderm posterior 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:16554359 1323369 Mesp1 mesoderm posterior 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:10887078 1323369 Mesp1 mesoderm posterior 1 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:10393122 1323369 Mesp1 mesoderm posterior 1 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:9739106 1323369 Mesp1 mesoderm posterior 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:18832392 1323369 Mesp1 mesoderm posterior 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20160218 MGI PMID:24748541 1323369 Mesp1 mesoderm posterior 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:16554359 1323369 Mesp1 mesoderm posterior 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20231109 MGI PMID:34050709 1323369 Mesp1 mesoderm posterior 1 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20231109 MGI PMID:34050709 1323369 Mesp1 mesoderm posterior 1 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:16554359 1323369 Mesp1 mesoderm posterior 1 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:16720879 1323369 Mesp1 mesoderm posterior 1 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0003679 ear lobe hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10393122 1323369 Mesp1 mesoderm posterior 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9739106 1323369 Mesp1 mesoderm posterior 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160721 MGI PMID:26932671 1323369 Mesp1 mesoderm posterior 1 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:11578861 1323369 Mesp1 mesoderm posterior 1 gene MP:0004032 abnormal interventricular groove morphology IAGP N RGD:5509061 20231109 MGI PMID:34050709 1323369 Mesp1 mesoderm posterior 1 gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:16554359 1323369 Mesp1 mesoderm posterior 1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:16554359 1323369 Mesp1 mesoderm posterior 1 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:16720879 1323369 Mesp1 mesoderm posterior 1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9739106 1323369 Mesp1 mesoderm posterior 1 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:10393122 1323369 Mesp1 mesoderm posterior 1 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:9739106 1323369 Mesp1 mesoderm posterior 1 gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9739106 1323369 Mesp1 mesoderm posterior 1 gene MP:0004555 pharynx hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0004569 glossopharyngeal nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:16996494 1323369 Mesp1 mesoderm posterior 1 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:16996494 1323369 Mesp1 mesoderm posterior 1 gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:9739106 1323369 Mesp1 mesoderm posterior 1 gene MP:0004937 dilated heart IAGP N RGD:5509061 20231109 MGI PMID:34050709 1323369 Mesp1 mesoderm posterior 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16554359 1323369 Mesp1 mesoderm posterior 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16720879 1323369 Mesp1 mesoderm posterior 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20231109 MGI PMID:34050709 1323369 Mesp1 mesoderm posterior 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16554359 1323369 Mesp1 mesoderm posterior 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16720879 1323369 Mesp1 mesoderm posterior 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:16720879 1323369 Mesp1 mesoderm posterior 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:18832392 1323369 Mesp1 mesoderm posterior 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231109 MGI PMID:34050709 1323369 Mesp1 mesoderm posterior 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:18547789 1323369 Mesp1 mesoderm posterior 1 gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:19855134 1323369 Mesp1 mesoderm posterior 1 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:19855134 1323369 Mesp1 mesoderm posterior 1 gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:10887078 1323369 Mesp1 mesoderm posterior 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:11578861 1323369 Mesp1 mesoderm posterior 1 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20231109 MGI PMID:34050709 1323369 Mesp1 mesoderm posterior 1 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10393122 1323369 Mesp1 mesoderm posterior 1 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:18547789 1323369 Mesp1 mesoderm posterior 1 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:18832392 1323369 Mesp1 mesoderm posterior 1 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0009490 abnormal heart left atrium auricular region morphology IAGP N RGD:5509061 20141003 MGI PMID:21089073 1323369 Mesp1 mesoderm posterior 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18440989 1323369 Mesp1 mesoderm posterior 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18832392 1323369 Mesp1 mesoderm posterior 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20160218 MGI PMID:24748541 1323369 Mesp1 mesoderm posterior 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20160218 MGI PMID:24748541 1323369 Mesp1 mesoderm posterior 1 gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:16720879 1323369 Mesp1 mesoderm posterior 1 gene MP:0010406 common atrium IAGP N RGD:5509061 20231109 MGI PMID:34050709 1323369 Mesp1 mesoderm posterior 1 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18832392 1323369 Mesp1 mesoderm posterior 1 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21089073 1323369 Mesp1 mesoderm posterior 1 gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20231109 MGI PMID:34050709 1323369 Mesp1 mesoderm posterior 1 gene MP:0010432 common ventricle IAGP N RGD:5509061 20141003 MGI PMID:16720879 1323369 Mesp1 mesoderm posterior 1 gene MP:0010432 common ventricle IAGP N RGD:5509061 20231109 MGI PMID:34050709 1323369 Mesp1 mesoderm posterior 1 gene MP:0010433 double inlet heart left ventricle IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0010453 abnormal coronary vein morphology IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0010455 aortopulmonary window IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20141003 MGI PMID:16720879 1323369 Mesp1 mesoderm posterior 1 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20141003 MGI PMID:18832392 1323369 Mesp1 mesoderm posterior 1 gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18547789 1323369 Mesp1 mesoderm posterior 1 gene MP:0010527 bicuspid pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:16720879 1323369 Mesp1 mesoderm posterior 1 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0010642 absent third pharyngeal arch IAGP N RGD:5509061 20171109 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0010643 absent fourth pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0010644 absent sixth pharyngeal arch IAGP N RGD:5509061 20171109 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20150910 MGI PMID:24895408 1323369 Mesp1 mesoderm posterior 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11578861 1323369 Mesp1 mesoderm posterior 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20150910 MGI PMID:24895408 1323369 Mesp1 mesoderm posterior 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10393122 1323369 Mesp1 mesoderm posterior 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10887078 1323369 Mesp1 mesoderm posterior 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16554359 1323369 Mesp1 mesoderm posterior 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9739106 1323369 Mesp1 mesoderm posterior 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160721 MGI PMID:26932671 1323369 Mesp1 mesoderm posterior 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:34050709 1323369 Mesp1 mesoderm posterior 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20160218 MGI PMID:24748541 1323369 Mesp1 mesoderm posterior 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16720879 1323369 Mesp1 mesoderm posterior 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20160218 MGI PMID:24748541 1323369 Mesp1 mesoderm posterior 1 gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:10887078 1323369 Mesp1 mesoderm posterior 1 gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:11578861 1323369 Mesp1 mesoderm posterior 1 gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20230713 MGI PMID:26102480 1323369 Mesp1 mesoderm posterior 1 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:9739106 1323369 Mesp1 mesoderm posterior 1 gene MP:0012184 absent paraxial mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10887078 1323369 Mesp1 mesoderm posterior 1 gene MP:0012278 abnormal cardiogenic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10393122 1323369 Mesp1 mesoderm posterior 1 gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0012757 abnormal cranial neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0013265 abnormal fourth pharyngeal pouch morphology IAGP N RGD:5509061 20150101 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0013268 second pharyngeal arch hypoplasia IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0013268 second pharyngeal arch hypoplasia IAGP N RGD:5509061 20171109 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0013269 third pharyngeal arch hypoplasia IAGP N RGD:5509061 20150924 MGI PMID:20035084 1323369 Mesp1 mesoderm posterior 1 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20230309 MGI PMID:23872235 1323369 Mesp1 mesoderm posterior 1 gene MP:0030334 absent sixth pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0030335 absent third pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:16914493 1323369 Mesp1 mesoderm posterior 1 gene MP:0030340 absent fourth pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:16914493 1323373 Prc1 protein regulator of cytokinesis 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1323373 Prc1 protein regulator of cytokinesis 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1323373 Prc1 protein regulator of cytokinesis 1 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1323373 Prc1 protein regulator of cytokinesis 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1323373 Prc1 protein regulator of cytokinesis 1 gene MP:0008762 embryonic lethality IEA N RGD:5509061 20141003 MGI 1323373 Prc1 protein regulator of cytokinesis 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1323373 Prc1 protein regulator of cytokinesis 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323375 Ctdp1 CTD phosphatase subunit 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20220310 MGI PMID:33408128 1323375 Ctdp1 CTD phosphatase subunit 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20220310 MGI PMID:33408128 1323375 Ctdp1 CTD phosphatase subunit 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20220310 MGI PMID:33408128 1323375 Ctdp1 CTD phosphatase subunit 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20220310 MGI PMID:33408128 1323375 Ctdp1 CTD phosphatase subunit 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20220310 MGI PMID:33408128 1323375 Ctdp1 CTD phosphatase subunit 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1323375 Ctdp1 CTD phosphatase subunit 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20220310 MGI PMID:33408128 1323375 Ctdp1 CTD phosphatase subunit 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230601 MGI 1323375 Ctdp1 CTD phosphatase subunit 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20230601 MGI 1323375 Ctdp1 CTD phosphatase subunit 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20220310 MGI PMID:33408128 1323377 Dglucy D-glutamate cyclase gene MP:0030736 increased glutamic acid level IAGP N RGD:5509061 20180927 MGI PMID:28266638 1323379 Rgp1 RAB6A GEF compex partner 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 1323379 Rgp1 RAB6A GEF compex partner 1 gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20210826 MGI 1323379 Rgp1 RAB6A GEF compex partner 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1323379 Rgp1 RAB6A GEF compex partner 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1323379 Rgp1 RAB6A GEF compex partner 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1323379 Rgp1 RAB6A GEF compex partner 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323379 Rgp1 RAB6A GEF compex partner 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1323379 Rgp1 RAB6A GEF compex partner 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1323379 Rgp1 RAB6A GEF compex partner 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1323381 Ddx41 DEAD box helicase 41 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 1323381 Ddx41 DEAD box helicase 41 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1323381 Ddx41 DEAD box helicase 41 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1323381 Ddx41 DEAD box helicase 41 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1323381 Ddx41 DEAD box helicase 41 gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:29871919 1323385 Rragc Ras-related GTP binding C gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323385 Rragc Ras-related GTP binding C gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323385 Rragc Ras-related GTP binding C gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323385 Rragc Ras-related GTP binding C gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323385 Rragc Ras-related GTP binding C gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323385 Rragc Ras-related GTP binding C gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323385 Rragc Ras-related GTP binding C gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323385 Rragc Ras-related GTP binding C gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323385 Rragc Ras-related GTP binding C gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323385 Rragc Ras-related GTP binding C gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323385 Rragc Ras-related GTP binding C gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323385 Rragc Ras-related GTP binding C gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323385 Rragc Ras-related GTP binding C gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323385 Rragc Ras-related GTP binding C gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323385 Rragc Ras-related GTP binding C gene MP:0020154 impaired humoral immune response IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323385 Rragc Ras-related GTP binding C gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20230601 MGI PMID:34260908 1323389 Arrdc4 arrestin domain containing 4 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20220519 MGI 1323389 Arrdc4 arrestin domain containing 4 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1323389 Arrdc4 arrestin domain containing 4 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20161208 MGI PMID:27462458 1323389 Arrdc4 arrestin domain containing 4 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20220519 MGI 1323389 Arrdc4 arrestin domain containing 4 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20231207 MGI 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0000599 enlarged liver IAGP N RGD:5509061 20160505 MGI PMID:21156282 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160505 MGI PMID:21156282 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20160505 MGI PMID:21156282 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:15750184 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:22733990 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20231207 MGI 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15750184 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:22733990 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:22987638 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:22987638 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:15750184 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:14563324 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:14563324 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15750184 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20160505 MGI PMID:21156282 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002083 premature death IAGP N RGD:5509061 20160505 MGI PMID:21156282 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002083 premature death IAGP N RGD:5509061 20190516 MGI PMID:28790031 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14563324 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19737919 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22733990 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002208 abnormal germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19737919 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14563324 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17000121 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14563324 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002747 abnormal aortic valve morphology IEA N RGD:5509061 20141003 MGI 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15750184 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20141003 MGI PMID:15937476 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22733990 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0004158 right aortic arch IEA N RGD:5509061 20141003 MGI 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20141003 MGI PMID:15750184 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22987638 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15750184 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:19737919 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19737919 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0004898 uterine hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22987638 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:19737919 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0005327 abnormal mesangial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0006339 abnormal third pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15750184 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15750184 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008093 abnormal memory B cell number IAGP N RGD:5509061 20141003 MGI PMID:14563324 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:14563324 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14563324 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20160505 MGI PMID:21156282 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008100 absent plasma cells IAGP N RGD:5509061 20141003 MGI PMID:22733990 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20160505 MGI PMID:21156282 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20160505 MGI PMID:21156282 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:15750184 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:15937476 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:19737919 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008393 absent primordial germ cells IAGP N RGD:5509061 20141003 MGI PMID:15750184 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:14563324 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:14563324 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160505 MGI PMID:21156282 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20160505 MGI PMID:21156282 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22987638 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20190516 MGI PMID:28790031 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20190516 MGI PMID:28790031 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20715164 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0010188 abnormal T follicular helper cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21948081 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0010466 vascular ring IEA N RGD:5509061 20141003 MGI 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0010488 abnormal left subclavian artery morphology IEA N RGD:5509061 20141003 MGI 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0010642 absent third pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15750184 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19737919 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15492122 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15750184 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22733990 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19737919 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0011262 abnormal pharyngeal arch mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:15750184 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20231207 MGI 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:19737919 1323392 Prdm1 PR domain containing 1, with ZNF domain gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:19664942 1323396 Dtx4 deltex 4, E3 ubiquitin ligase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200514 MGI 1323396 Dtx4 deltex 4, E3 ubiquitin ligase gene MP:0000274 enlarged heart IEA N RGD:5509061 20200514 MGI 1323396 Dtx4 deltex 4, E3 ubiquitin ligase gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20200514 MGI 1323396 Dtx4 deltex 4, E3 ubiquitin ligase gene MP:0000709 enlarged thymus IEA N RGD:5509061 20200514 MGI 1323396 Dtx4 deltex 4, E3 ubiquitin ligase gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1323396 Dtx4 deltex 4, E3 ubiquitin ligase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1323396 Dtx4 deltex 4, E3 ubiquitin ligase gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220519 MGI 1323396 Dtx4 deltex 4, E3 ubiquitin ligase gene MP:0010935 increased airway resistance IEA N RGD:5509061 20220519 MGI 1323396 Dtx4 deltex 4, E3 ubiquitin ligase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1323407 Nt5el 5' nucleotidase, ecto-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160915 MGI PMID:24652767 1323412 Tpcn2 two pore segment channel 2 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20230420 MGI PMID:36641477 1323412 Tpcn2 two pore segment channel 2 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20201022 MGI 1323412 Tpcn2 two pore segment channel 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26769314 1323412 Tpcn2 two pore segment channel 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:23063126 1323412 Tpcn2 two pore segment channel 2 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20230420 MGI PMID:36641477 1323412 Tpcn2 two pore segment channel 2 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19387438 1323412 Tpcn2 two pore segment channel 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1323412 Tpcn2 two pore segment channel 2 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20230420 MGI PMID:36641477 1323412 Tpcn2 two pore segment channel 2 gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20230420 MGI PMID:36641477 1323412 Tpcn2 two pore segment channel 2 gene MP:0005391 vision/eye phenotype IAGP N RGD:5509061 20230420 MGI PMID:36641477 1323412 Tpcn2 two pore segment channel 2 gene MP:0010190 abnormal retina melanocyte morphology IAGP N RGD:5509061 20230420 MGI PMID:36641477 1323412 Tpcn2 two pore segment channel 2 gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20230420 MGI PMID:36641477 1323413 Mrm1 mitochondrial rRNA methyltransferase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1323415 Casp14 caspase 14 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1323415 Casp14 caspase 14 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1323415 Casp14 caspase 14 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1323415 Casp14 caspase 14 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:17515931 1323415 Casp14 caspase 14 gene MP:0001203 increased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:17515931 1323415 Casp14 caspase 14 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:17515931 1323415 Casp14 caspase 14 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:18156206 1323415 Casp14 caspase 14 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:17515931 1323415 Casp14 caspase 14 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1323415 Casp14 caspase 14 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:17515931 1323415 Casp14 caspase 14 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20210128 MGI 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:19046572 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20150205 MGI PMID:24497849 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19046572 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:21179166 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21179166 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:21179166 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20210415 MGI PMID:29967452 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:19046572 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19046572 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19046572 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:19046572 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19046572 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19046572 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:21179166 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20150205 MGI PMID:24497849 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19046572 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19046572 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20211021 MGI 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0004130 abnormal muscle cell glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:19046572 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:19046572 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20150205 MGI PMID:24497849 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17141160 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0005068 abnormal NK cell morphology IAGP N RGD:5509061 20210415 MGI PMID:29967452 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20150205 MGI PMID:24497849 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0006420 abnormal peritubular myoid cell morphology IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0006428 ectopic Sertoli cells IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20210415 MGI PMID:29967452 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22504639 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:22504639 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19046572 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:22504639 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:19046572 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19046571 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17141160 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:19046572 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:17141160 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:22504639 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0020355 abnormal Sertoli cell barrier morphology IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323418 Rptor regulatory associated protein of MTOR, complex 1 gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20201022 MGI PMID:29961810 1323419 Foxred1 FAD-dependent oxidoreductase domain containing 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1323419 Foxred1 FAD-dependent oxidoreductase domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323419 Foxred1 FAD-dependent oxidoreductase domain containing 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1323428 Arpc5 actin related protein 2/3 complex, subunit 5 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20230831 MGI PMID:37382373 1323428 Arpc5 actin related protein 2/3 complex, subunit 5 gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20230831 MGI PMID:37382373 1323428 Arpc5 actin related protein 2/3 complex, subunit 5 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20230831 MGI PMID:37382373 1323428 Arpc5 actin related protein 2/3 complex, subunit 5 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20230831 MGI PMID:37382373 1323428 Arpc5 actin related protein 2/3 complex, subunit 5 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20230831 MGI PMID:37382373 1323428 Arpc5 actin related protein 2/3 complex, subunit 5 gene MP:0012707 incomplete caudal neuropore closure IAGP N RGD:5509061 20230831 MGI PMID:37382373 1323428 Arpc5 actin related protein 2/3 complex, subunit 5 gene MP:0014044 absent cardiac outflow tract IAGP N RGD:5509061 20230831 MGI PMID:37382373 1323430 Pidd1 p53 induced death domain protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19364921 1323435 Zfp280d zinc finger protein 280D gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1323435 Zfp280d zinc finger protein 280D gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20210520 MGI 1323435 Zfp280d zinc finger protein 280D gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210520 MGI 1323435 Zfp280d zinc finger protein 280D gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20210826 MGI 1323435 Zfp280d zinc finger protein 280D gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20221215 MGI 1323435 Zfp280d zinc finger protein 280D gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20210826 MGI 1323435 Zfp280d zinc finger protein 280D gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210520 MGI 1323435 Zfp280d zinc finger protein 280D gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1323435 Zfp280d zinc finger protein 280D gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210826 MGI 1323435 Zfp280d zinc finger protein 280D gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 1323435 Zfp280d zinc finger protein 280D gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20211021 MGI 1323435 Zfp280d zinc finger protein 280D gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210520 MGI 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16597604 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16287712 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:23102580 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:23102580 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:23102580 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:23102581 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:23102580 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:23102581 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:23102580 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16287712 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0002534 abnormal type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11371360 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16287712 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:23102580 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:23102581 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0002996 ovotestis IAGP N RGD:5509061 20141003 MGI PMID:23102580 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:23102580 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:23102581 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:16287712 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:16287712 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:11371360 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16597604 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0006424 absent testis cords IAGP N RGD:5509061 20141003 MGI PMID:23102581 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16287712 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14691480 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16287712 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16287712 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11371360 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:14691480 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:23102580 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14691480 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20180118 MGI PMID:25071184 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180118 MGI PMID:25071184 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20180118 MGI PMID:25071184 1323437 Gadd45g growth arrest and DNA-damage-inducible 45 gamma gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:16287712 1323440 Ddx55 DEAD box helicase 55 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201022 MGI 1323440 Ddx55 DEAD box helicase 55 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1323440 Ddx55 DEAD box helicase 55 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323442 Fermt2 fermitin family member 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20160929 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0000075 absent neurocranium IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20160929 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160929 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:18483218 1323442 Fermt2 fermitin family member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160929 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20160929 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20160929 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20160929 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0003109 short femur IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:18483218 1323442 Fermt2 fermitin family member 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:18483218 1323442 Fermt2 fermitin family member 2 gene MP:0004321 short sternum IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0004338 small clavicle IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0004340 short scapula IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0004355 short radius IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20160929 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0004626 vertebral compression IAGP N RGD:5509061 20160929 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0008817 hematoma IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20160929 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20160929 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18174465 1323442 Fermt2 fermitin family member 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18483218 1323442 Fermt2 fermitin family member 2 gene MP:0012279 wide sternum IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20160929 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323442 Fermt2 fermitin family member 2 gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20160922 MGI PMID:26151572 1323443 Stbd1 starch binding domain 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1323443 Stbd1 starch binding domain 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20211028 MGI PMID:27358407 1323443 Stbd1 starch binding domain 1 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20211028 MGI PMID:27358407 1323443 Stbd1 starch binding domain 1 gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20211028 MGI PMID:27358407 1323445 Syngr3 synaptogyrin 3 gene MP:0002064 seizures IEA N RGD:5509061 20150219 MGI 1323445 Syngr3 synaptogyrin 3 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20210422 MGI PMID:33472038 1323445 Syngr3 synaptogyrin 3 gene MP:0008918 microgliosis IAGP N RGD:5509061 20210422 MGI PMID:33472038 1323452 Hspa9 heat shock protein 9 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20160225 MGI PMID:25550197 1323452 Hspa9 heat shock protein 9 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160225 MGI PMID:25550197 1323456 Tpgs1 tubulin polyglutamylase complex subunit 1 gene MP:0001355 submission towards male mice IAGP N RGD:5509061 20141003 MGI PMID:12242242 1323456 Tpgs1 tubulin polyglutamylase complex subunit 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12242242 1323456 Tpgs1 tubulin polyglutamylase complex subunit 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12242242 1323456 Tpgs1 tubulin polyglutamylase complex subunit 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12242242 1323456 Tpgs1 tubulin polyglutamylase complex subunit 1 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:12242242 1323456 Tpgs1 tubulin polyglutamylase complex subunit 1 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20141003 MGI PMID:12242242 1323456 Tpgs1 tubulin polyglutamylase complex subunit 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12242242 1323456 Tpgs1 tubulin polyglutamylase complex subunit 1 gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20220811 MGI PMID:12242242 1323459 Mab21l2 mab-21-like 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1323459 Mab21l2 mab-21-like 2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1323459 Mab21l2 mab-21-like 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1323459 Mab21l2 mab-21-like 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:15385160 1323459 Mab21l2 mab-21-like 2 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 1323459 Mab21l2 mab-21-like 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1323459 Mab21l2 mab-21-like 2 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20230601 MGI 1323459 Mab21l2 mab-21-like 2 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:15385160 1323459 Mab21l2 mab-21-like 2 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:15385160 1323459 Mab21l2 mab-21-like 2 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20220519 MGI 1323459 Mab21l2 mab-21-like 2 gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:15385160 1323459 Mab21l2 mab-21-like 2 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:15385160 1323459 Mab21l2 mab-21-like 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1323459 Mab21l2 mab-21-like 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15385160 1323459 Mab21l2 mab-21-like 2 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20231207 MGI 1323459 Mab21l2 mab-21-like 2 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:15385160 1323459 Mab21l2 mab-21-like 2 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15385160 1323459 Mab21l2 mab-21-like 2 gene MP:0009725 absent lens vesicle IAGP N RGD:5509061 20141003 MGI PMID:15385160 1323459 Mab21l2 mab-21-like 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15385160 1323459 Mab21l2 mab-21-like 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323459 Mab21l2 mab-21-like 2 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1323461 Ccrl2 C-C motif chemokine receptor-like 2 gene MP:0002148 abnormal hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:20606167 1323461 Ccrl2 C-C motif chemokine receptor-like 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1323461 Ccrl2 C-C motif chemokine receptor-like 2 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:20606167 1323461 Ccrl2 C-C motif chemokine receptor-like 2 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18794339 1323461 Ccrl2 C-C motif chemokine receptor-like 2 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20606167 1323461 Ccrl2 C-C motif chemokine receptor-like 2 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:20606167 1323461 Ccrl2 C-C motif chemokine receptor-like 2 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20606167 1323461 Ccrl2 C-C motif chemokine receptor-like 2 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:20606167 1323461 Ccrl2 C-C motif chemokine receptor-like 2 gene MP:0010740 abnormal dendritic cell chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20606167 1323463 Ferd3l Fer3 like bHLH transcription factor gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20460368 1323463 Ferd3l Fer3 like bHLH transcription factor gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:20460368 1323463 Ferd3l Fer3 like bHLH transcription factor gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:20460368 1323463 Ferd3l Fer3 like bHLH transcription factor gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:20460368 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0001304 cataract IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0001314 cornea opacity IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20201105 MGI PMID:30333725 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20201105 MGI PMID:30333725 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20201105 MGI PMID:30333725 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20201105 MGI PMID:30333725 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0001785 edema IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0002083 premature death IAGP N RGD:5509061 20201105 MGI PMID:30333725 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20201105 MGI PMID:30333725 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0002989 small kidney IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20201105 MGI PMID:30333725 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20201105 MGI PMID:30333725 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20201105 MGI PMID:30333725 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0012507 midbrain atrophy IAGP N RGD:5509061 20201105 MGI PMID:30333725 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0013272 abnormal translation IAGP N RGD:5509061 20201105 MGI PMID:30333725 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20201105 MGI PMID:30333725 1323466 Eef1d eukaryotic translation elongation factor 1 delta gene MP:0030003 hippocampus atrophy IAGP N RGD:5509061 20201105 MGI PMID:30333725 1323467 Ddi2 DNA-damage inducible protein 2 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20200514 MGI 1323467 Ddi2 DNA-damage inducible protein 2 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20200514 MGI 1323467 Ddi2 DNA-damage inducible protein 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1323467 Ddi2 DNA-damage inducible protein 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1323467 Ddi2 DNA-damage inducible protein 2 gene MP:0010935 increased airway resistance IEA N RGD:5509061 20211021 MGI 1323467 Ddi2 DNA-damage inducible protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323467 Ddi2 DNA-damage inducible protein 2 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20210826 MGI 1323469 Polr3d polymerase (RNA) III (DNA directed) polypeptide D gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1323469 Polr3d polymerase (RNA) III (DNA directed) polypeptide D gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1323469 Polr3d polymerase (RNA) III (DNA directed) polypeptide D gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20211021 MGI 1323469 Polr3d polymerase (RNA) III (DNA directed) polypeptide D gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20220519 MGI 1323469 Polr3d polymerase (RNA) III (DNA directed) polypeptide D gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 1323469 Polr3d polymerase (RNA) III (DNA directed) polypeptide D gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1323469 Polr3d polymerase (RNA) III (DNA directed) polypeptide D gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1323471 Cpox coproporphyrinogen oxidase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180628 MGI PMID:28600349 1323471 Cpox coproporphyrinogen oxidase gene MP:0000929 open neural tube IAGP N RGD:5509061 20180628 MGI PMID:28600349 1323471 Cpox coproporphyrinogen oxidase gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:4853271 1323471 Cpox coproporphyrinogen oxidase gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:672986 1323471 Cpox coproporphyrinogen oxidase gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:12470976 1323471 Cpox coproporphyrinogen oxidase gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:23631845 1323471 Cpox coproporphyrinogen oxidase gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:4853271 1323471 Cpox coproporphyrinogen oxidase gene MP:0001309 hydropic eye lens fibers IAGP N RGD:5509061 20141003 MGI PMID:4853271 1323471 Cpox coproporphyrinogen oxidase gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20180628 MGI PMID:28600349 1323471 Cpox coproporphyrinogen oxidase gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20180628 MGI PMID:28600349 1323471 Cpox coproporphyrinogen oxidase gene MP:0002642 anisocytosis IEA N RGD:5509061 20221201 MGI 1323471 Cpox coproporphyrinogen oxidase gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20180628 MGI PMID:28600349 1323471 Cpox coproporphyrinogen oxidase gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:4853271 1323471 Cpox coproporphyrinogen oxidase gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20180628 MGI PMID:28600349 1323471 Cpox coproporphyrinogen oxidase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180628 MGI PMID:28600349 1323471 Cpox coproporphyrinogen oxidase gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20221201 MGI 1323471 Cpox coproporphyrinogen oxidase gene MP:0005654 porphyria IAGP N RGD:5509061 20180628 MGI PMID:28600349 1323471 Cpox coproporphyrinogen oxidase gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20180628 MGI PMID:28600349 1323471 Cpox coproporphyrinogen oxidase gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20180628 MGI PMID:28600349 1323471 Cpox coproporphyrinogen oxidase gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20180628 MGI PMID:28600349 1323471 Cpox coproporphyrinogen oxidase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180628 MGI PMID:28600349 1323471 Cpox coproporphyrinogen oxidase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1323471 Cpox coproporphyrinogen oxidase gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20180628 MGI PMID:28600349 1323471 Cpox coproporphyrinogen oxidase gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20180628 MGI PMID:28600349 1323471 Cpox coproporphyrinogen oxidase gene MP:0013165 absent forelimb buds IAGP N RGD:5509061 20180628 MGI PMID:28600349 1323475 Pop5 processing of precursor 5, ribonuclease P/MRP family (S. cerevisiae) gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240926 MGI 1323475 Pop5 processing of precursor 5, ribonuclease P/MRP family (S. cerevisiae) gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241017 MGI 1323475 Pop5 processing of precursor 5, ribonuclease P/MRP family (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1323475 Pop5 processing of precursor 5, ribonuclease P/MRP family (S. cerevisiae) gene MP:0012111 failure of morula compaction IEA N RGD:5509061 20240926 MGI 1323475 Pop5 processing of precursor 5, ribonuclease P/MRP family (S. cerevisiae) gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20240926 MGI 1323475 Pop5 processing of precursor 5, ribonuclease P/MRP family (S. cerevisiae) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1323477 Rasal1 RAS protein activator like 1 (GAP1 like) gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20210729 MGI PMID:30158531 1323480 Gstcd glutathione S-transferase, C-terminal domain containing gene MP:0000691 enlarged spleen IEA N RGD:5509061 20190502 MGI 1323480 Gstcd glutathione S-transferase, C-terminal domain containing gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20191128 MGI PMID:31513609 1323480 Gstcd glutathione S-transferase, C-terminal domain containing gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20201022 MGI 1323480 Gstcd glutathione S-transferase, C-terminal domain containing gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20211021 MGI 1323480 Gstcd glutathione S-transferase, C-terminal domain containing gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20191128 MGI PMID:31513609 1323481 Prss37 serine protease 37 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:23553430 1323481 Prss37 serine protease 37 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23553430 1323481 Prss37 serine protease 37 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20220303 MGI PMID:23553430 1323481 Prss37 serine protease 37 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220303 MGI PMID:23553430 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0000743 muscle spasm IEA N RGD:5509061 20141003 MGI 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19436707 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20180621 MGI PMID:24358326 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20240801 MGI PMID:24358326 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0000749 muscle degeneration IEA N RGD:5509061 20141003 MGI 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:7416502 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20141003 MGI 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20180621 MGI PMID:24358326 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180621 MGI PMID:24358326 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180621 MGI PMID:24358326 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0001393 ataxia IAGP N RGD:5509061 20240801 MGI PMID:24358326 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180621 MGI PMID:24358326 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12368914 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0001513 limb grasping IEA N RGD:5509061 20141003 MGI 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0001732 postnatal growth retardation IEA N RGD:5509061 20111116 MGI 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:12368914 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0001926 female infertility IEA N RGD:5509061 20111116 MGI 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20240801 MGI PMID:24358326 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0002083 premature death IAGP N RGD:5509061 20180621 MGI PMID:24358326 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:18771733 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:12368914 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:18771733 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0002922 decreased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:12368914 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10889334 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0003225 axonal dystrophy IEA N RGD:5509061 20141003 MGI 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0003415 priapism IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20180621 MGI PMID:24358326 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12368914 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10889334 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0004166 abnormal limbic system morphology IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0004708 short lumbar vertebrae IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:12368914 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0005277 abnormal brainstem morphology IEA N RGD:5509061 20141003 MGI 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:12368914 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0008222 decreased hippocampal commissure size IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0008232 abnormal cingulum morphology IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:7416502 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0009434 paraparesis IEA N RGD:5509061 20141003 MGI 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7416502 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180621 MGI PMID:24358326 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0020560 abnormal pontine nuclei morphology IAGP N RGD:5509061 20180315 MGI PMID:5855800 1323484 Usp14 ubiquitin specific peptidase 14 gene MP:0020955 increased mechanical nociceptive threshold IAGP N RGD:5509061 20211230 MGI PMID:24358326 1323486 Rcan3 regulator of calcineurin 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240523 MGI 1323486 Rcan3 regulator of calcineurin 3 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20221215 MGI 1323488 Rhbdd3 rhomboid domain containing 3 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:23610400 1323488 Rhbdd3 rhomboid domain containing 3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:23610400 1323488 Rhbdd3 rhomboid domain containing 3 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23610400 1323488 Rhbdd3 rhomboid domain containing 3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23610400 1323488 Rhbdd3 rhomboid domain containing 3 gene MP:0003080 increased natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:23610400 1323488 Rhbdd3 rhomboid domain containing 3 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23610400 1323488 Rhbdd3 rhomboid domain containing 3 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:23610400 1323488 Rhbdd3 rhomboid domain containing 3 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23610400 1323488 Rhbdd3 rhomboid domain containing 3 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:23610400 1323488 Rhbdd3 rhomboid domain containing 3 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:23610400 1323488 Rhbdd3 rhomboid domain containing 3 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:23610400 1323488 Rhbdd3 rhomboid domain containing 3 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23610400 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20221117 MGI PMID:33481887 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20221117 MGI PMID:33481887 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17577922 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:17577922 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20221117 MGI PMID:33481887 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20221117 MGI PMID:33481887 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17577922 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:7926766 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17577922 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17577922 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:7926766 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20221117 MGI PMID:33481887 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17577922 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:17577922 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20150326 MGI PMID:7926766 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20150326 MGI PMID:7926766 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:17577922 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20221117 MGI PMID:33481887 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20221117 MGI PMID:33481887 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:7926766 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:7926766 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7926766 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20221117 MGI PMID:33481887 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20221117 MGI PMID:33481887 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17577922 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:7926766 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20221117 MGI PMID:33481887 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0011286 decreased circulating erythropoietin level IAGP N RGD:5509061 20221117 MGI PMID:33481887 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0013660 abnormal bone marrow hematopoietic cell morphology IAGP N RGD:5509061 20221117 MGI PMID:33481887 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0020421 increased freezing behavior IAGP N RGD:5509061 20170720 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20180301 MGI PMID:28604739 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0031051 lymph node hemorrhage IAGP N RGD:5509061 20200618 MGI PMID:17577922 1323494 Lrfn2 leucine rich repeat and fibronectin type III domain containing 2 gene MP:0031052 lymph node necrosis IAGP N RGD:5509061 20200618 MGI PMID:17577922 1323496 Gpr65 G-protein coupled receptor 65 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1323496 Gpr65 G-protein coupled receptor 65 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1323496 Gpr65 G-protein coupled receptor 65 gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15665078 1323496 Gpr65 G-protein coupled receptor 65 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20170105 MGI 1323496 Gpr65 G-protein coupled receptor 65 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15665078 1323496 Gpr65 G-protein coupled receptor 65 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:19234222 1323496 Gpr65 G-protein coupled receptor 65 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170105 MGI 1323496 Gpr65 G-protein coupled receptor 65 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 1323496 Gpr65 G-protein coupled receptor 65 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20170105 MGI 1323496 Gpr65 G-protein coupled receptor 65 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:24221084 1323496 Gpr65 G-protein coupled receptor 65 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19234222 1323496 Gpr65 G-protein coupled receptor 65 gene MP:0008656 abnormal interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:24447140 1323496 Gpr65 G-protein coupled receptor 65 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1323496 Gpr65 G-protein coupled receptor 65 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:24221084 1323496 Gpr65 G-protein coupled receptor 65 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:24221084 1323498 Pals2 protein associated with LIN7 2, MAGUK family member gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20220519 MGI 1323498 Pals2 protein associated with LIN7 2, MAGUK family member gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1323498 Pals2 protein associated with LIN7 2, MAGUK family member gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 1323498 Pals2 protein associated with LIN7 2, MAGUK family member gene MP:0002764 short tibia IEA N RGD:5509061 20220519 MGI 1323498 Pals2 protein associated with LIN7 2, MAGUK family member gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220519 MGI 1323498 Pals2 protein associated with LIN7 2, MAGUK family member gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20220519 MGI 1323498 Pals2 protein associated with LIN7 2, MAGUK family member gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220519 MGI 1323498 Pals2 protein associated with LIN7 2, MAGUK family member gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220519 MGI 1323504 Zpr1 ZPR1 zinc finger gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:15767679 1323504 Zpr1 ZPR1 zinc finger gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15767679 1323504 Zpr1 ZPR1 zinc finger gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15767679 1323504 Zpr1 ZPR1 zinc finger gene MP:0008888 abnormal Cajal body morphology IAGP N RGD:5509061 20141003 MGI PMID:15767679 1323504 Zpr1 ZPR1 zinc finger gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15767679 1323504 Zpr1 ZPR1 zinc finger gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15767679 1323504 Zpr1 ZPR1 zinc finger gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:15767679 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0000879 increased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0001061 abnormal oculomotor nerve morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0001063 abnormal trochlear nerve morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0001177 atelectasis IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0004592 small mandible IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0004612 fusion of vertebral bodies IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0010008 abnormal Purkinje cell migration IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0013551 decreased cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20161201 MGI PMID:22357600 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0013848 subcutaneous edema IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0014167 ectopic bone IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20221013 MGI PMID:31241461 1323506 Rbfox2 RNA binding protein, fox-1 homolog (C. elegans) 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:31241461 1323509 Dok3 docking protein 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20139980 1323509 Dok3 docking protein 3 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20548287 1323509 Dok3 docking protein 3 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20139980 1323509 Dok3 docking protein 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20139980 1323509 Dok3 docking protein 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20548287 1323509 Dok3 docking protein 3 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:20139980 1323509 Dok3 docking protein 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20548287 1323509 Dok3 docking protein 3 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20191128 MGI PMID:17363732 1323509 Dok3 docking protein 3 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20191128 MGI PMID:17363732 1323509 Dok3 docking protein 3 gene MP:0004202 pulmonary hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20139980 1323509 Dok3 docking protein 3 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20191128 MGI PMID:17363732 1323509 Dok3 docking protein 3 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:20548287 1323509 Dok3 docking protein 3 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:20139980 1323509 Dok3 docking protein 3 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20139980 1323509 Dok3 docking protein 3 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20191128 MGI PMID:17363732 1323509 Dok3 docking protein 3 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20548287 1323509 Dok3 docking protein 3 gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:20139980 1323509 Dok3 docking protein 3 gene MP:0010829 increased bronchioalveolar stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20139980 1323509 Dok3 docking protein 3 gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:17363732 1323509 Dok3 docking protein 3 gene MP:0020155 enhanced humoral immune response IAGP N RGD:5509061 20191128 MGI PMID:17363732 1323510 Akr1c21 aldo-keto reductase family 1, member C21 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20240530 MGI PMID:34590152 1323510 Akr1c21 aldo-keto reductase family 1, member C21 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20240530 MGI PMID:34590152 1323510 Akr1c21 aldo-keto reductase family 1, member C21 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20240530 MGI PMID:34590152 1323510 Akr1c21 aldo-keto reductase family 1, member C21 gene MP:0014437 increased interleukin level IAGP N RGD:5509061 20240530 MGI PMID:34590152 1323513 N6amt1 N-6 adenine-specific DNA methyltransferase 1 (putative) gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20606008 1323513 N6amt1 N-6 adenine-specific DNA methyltransferase 1 (putative) gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:20606008 1323513 N6amt1 N-6 adenine-specific DNA methyltransferase 1 (putative) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20606008 1323513 N6amt1 N-6 adenine-specific DNA methyltransferase 1 (putative) gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:20606008 1323513 N6amt1 N-6 adenine-specific DNA methyltransferase 1 (putative) gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:20606008 1323513 N6amt1 N-6 adenine-specific DNA methyltransferase 1 (putative) gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20606008 1323515 Orc2 origin recognition complex, subunit 2 gene MP:0001513 limb grasping IEA N RGD:5509061 20220811 MGI 1323515 Orc2 origin recognition complex, subunit 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1323515 Orc2 origin recognition complex, subunit 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323515 Orc2 origin recognition complex, subunit 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 1323519 1700030K09Rik RIKEN cDNA 1700030K09 gene gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1323519 1700030K09Rik RIKEN cDNA 1700030K09 gene gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 1323520 P4htm prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum) gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:22955912 1323520 P4htm prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum) gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22955912 1323520 P4htm prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum) gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:22955912 1323520 P4htm prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum) gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:22955912 1323520 P4htm prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum) gene MP:0011286 decreased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:22955912 1323521 Focad focadhesin gene MP:0000111 cleft palate IEA N RGD:5509061 20210826 MGI 1323521 Focad focadhesin gene MP:0001293 anophthalmia IEA N RGD:5509061 20210826 MGI 1323521 Focad focadhesin gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210826 MGI 1323521 Focad focadhesin gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20210826 MGI 1323521 Focad focadhesin gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20210826 MGI 1323521 Focad focadhesin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1323523 Nrip1 nuclear receptor interacting protein 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:24667635 1323523 Nrip1 nuclear receptor interacting protein 1 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11100122 1323523 Nrip1 nuclear receptor interacting protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11100122 1323523 Nrip1 nuclear receptor interacting protein 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11100122 1323523 Nrip1 nuclear receptor interacting protein 1 gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20141003 MGI PMID:11100122 1323523 Nrip1 nuclear receptor interacting protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24667635 1323523 Nrip1 nuclear receptor interacting protein 1 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:11100122 1323523 Nrip1 nuclear receptor interacting protein 1 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24667635 1323523 Nrip1 nuclear receptor interacting protein 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:24667635 1323523 Nrip1 nuclear receptor interacting protein 1 gene MP:0008869 anovulation IAGP N RGD:5509061 20220804 MGI PMID:11100122 1323523 Nrip1 nuclear receptor interacting protein 1 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:24667635 1323523 Nrip1 nuclear receptor interacting protein 1 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24667635 1323523 Nrip1 nuclear receptor interacting protein 1 gene MP:0009648 abnormal superovulation IAGP N RGD:5509061 20220804 MGI PMID:11100122 1323523 Nrip1 nuclear receptor interacting protein 1 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:11100122 1323523 Nrip1 nuclear receptor interacting protein 1 gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220804 MGI PMID:11100122 1323528 Laptm4b lysosomal-associated protein transmembrane 4B gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20181227 MGI 1323528 Laptm4b lysosomal-associated protein transmembrane 4B gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20181227 MGI 1323528 Laptm4b lysosomal-associated protein transmembrane 4B gene MP:0000897 abnormal midbrain morphology IEA N RGD:5509061 20181227 MGI 1323528 Laptm4b lysosomal-associated protein transmembrane 4B gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 1323528 Laptm4b lysosomal-associated protein transmembrane 4B gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20170105 MGI 1323528 Laptm4b lysosomal-associated protein transmembrane 4B gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1323528 Laptm4b lysosomal-associated protein transmembrane 4B gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1323528 Laptm4b lysosomal-associated protein transmembrane 4B gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20211125 MGI PMID:32693673 1323528 Laptm4b lysosomal-associated protein transmembrane 4B gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20170105 MGI 1323528 Laptm4b lysosomal-associated protein transmembrane 4B gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20211125 MGI PMID:32693673 1323528 Laptm4b lysosomal-associated protein transmembrane 4B gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20170105 MGI 1323528 Laptm4b lysosomal-associated protein transmembrane 4B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 1323528 Laptm4b lysosomal-associated protein transmembrane 4B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 1323528 Laptm4b lysosomal-associated protein transmembrane 4B gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20211125 MGI PMID:32693673 1323535 Abhd4 abhydrolase domain containing 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1323535 Abhd4 abhydrolase domain containing 4 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200416 MGI PMID:25853435 1323535 Abhd4 abhydrolase domain containing 4 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200416 MGI PMID:25853435 1323538 Scoc short coiled-coil protein gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20230601 MGI 1323538 Scoc short coiled-coil protein gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220519 MGI 1323538 Scoc short coiled-coil protein gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20231207 MGI 1323538 Scoc short coiled-coil protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1323540 Nudt16l1 nudix hydrolase 16 like 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1323540 Nudt16l1 nudix hydrolase 16 like 1 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1323540 Nudt16l1 nudix hydrolase 16 like 1 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1323540 Nudt16l1 nudix hydrolase 16 like 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1323542 Carnmt1 carnosine N-methyltransferase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20231102 MGI PMID:37612136 1323542 Carnmt1 carnosine N-methyltransferase 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20231102 MGI PMID:37612136 1323542 Carnmt1 carnosine N-methyltransferase 1 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20231102 MGI PMID:37612136 1323544 Slc22a12 solute carrier family 22 (organic anion/cation transporter), member 12 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18270321 1323544 Slc22a12 solute carrier family 22 (organic anion/cation transporter), member 12 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18270321 1323544 Slc22a12 solute carrier family 22 (organic anion/cation transporter), member 12 gene MP:0009810 increased urine uric acid level IAGP N RGD:5509061 20180517 MGI PMID:20544513 1323544 Slc22a12 solute carrier family 22 (organic anion/cation transporter), member 12 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20180517 MGI PMID:20544513 1323544 Slc22a12 solute carrier family 22 (organic anion/cation transporter), member 12 gene MP:0011537 uraturia IAGP N RGD:5509061 20141003 MGI PMID:18270321 1323546 Mtmr2 myotubularin related protein 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:15557122 1323546 Mtmr2 myotubularin related protein 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15557122 1323546 Mtmr2 myotubularin related protein 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15557122 1323546 Mtmr2 myotubularin related protein 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:16249189 1323546 Mtmr2 myotubularin related protein 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15557122 1323546 Mtmr2 myotubularin related protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15557122 1323546 Mtmr2 myotubularin related protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17855448 1323546 Mtmr2 myotubularin related protein 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15557122 1323546 Mtmr2 myotubularin related protein 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230119 MGI 1323546 Mtmr2 myotubularin related protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15557122 1323546 Mtmr2 myotubularin related protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16249189 1323546 Mtmr2 myotubularin related protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:17855448 1323546 Mtmr2 myotubularin related protein 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1323546 Mtmr2 myotubularin related protein 2 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 1323546 Mtmr2 myotubularin related protein 2 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15557122 1323546 Mtmr2 myotubularin related protein 2 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20230119 MGI 1323546 Mtmr2 myotubularin related protein 2 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:15557122 1323546 Mtmr2 myotubularin related protein 2 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:15557122 1323546 Mtmr2 myotubularin related protein 2 gene MP:0010540 long stride length IAGP N RGD:5509061 20141003 MGI PMID:15557122 1323546 Mtmr2 myotubularin related protein 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15557122 1323547 Cyp2r1 cytochrome P450, family 2, subfamily r, polypeptide 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20170223 MGI PMID:24019477 1323547 Cyp2r1 cytochrome P450, family 2, subfamily r, polypeptide 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20170223 MGI PMID:24019477 1323547 Cyp2r1 cytochrome P450, family 2, subfamily r, polypeptide 1 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20170223 MGI PMID:24019477 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:17339376 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0001147 small testis IEA N RGD:5509061 20220519 MGI 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21478856 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17339376 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17339376 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0002989 small kidney IEA N RGD:5509061 20220519 MGI 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17339376 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0004930 small epididymis IEA N RGD:5509061 20220519 MGI 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:17339376 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17339376 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17339376 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1323548 Syce2 synaptonemal complex central element protein 2 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1323549 Cenpl centromere protein L gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20201231 MGI 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20240523 MGI 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20191107 MGI PMID:28475869 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0004094 abnormal M line morphology IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0004937 dilated heart IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20191107 MGI PMID:28475869 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20191107 MGI PMID:28475869 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20191107 MGI PMID:28475869 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0010509 decreased P wave amplitude IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0010511 shortened PR interval IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0010634 increased QRS amplitude IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0030567 abnormal I band morphology IAGP N RGD:5509061 20191107 MGI PMID:29183906 1323551 Smarcd3 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:29183906 1323552 Tex46 testis expressed 46 gene MP:0001147 small testis IAGP N RGD:5509061 20241114 MGI PMID:38516277 1323552 Tex46 testis expressed 46 gene MP:0001925 male infertility IAGP N RGD:5509061 20241114 MGI PMID:38516277 1323552 Tex46 testis expressed 46 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20241114 MGI PMID:38516277 1323552 Tex46 testis expressed 46 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20241114 MGI PMID:38516277 1323552 Tex46 testis expressed 46 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20241114 MGI PMID:38516277 1323552 Tex46 testis expressed 46 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20241114 MGI PMID:38516277 1323552 Tex46 testis expressed 46 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20241114 MGI PMID:38516277 1323552 Tex46 testis expressed 46 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20241114 MGI PMID:38516277 1323552 Tex46 testis expressed 46 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20241114 MGI PMID:38516277 1323554 Pus1 pseudouridine synthase 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1323554 Pus1 pseudouridine synthase 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1323554 Pus1 pseudouridine synthase 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1323554 Pus1 pseudouridine synthase 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1323554 Pus1 pseudouridine synthase 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20161222 MGI PMID:27197761 1323554 Pus1 pseudouridine synthase 1 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20220811 MGI 1323554 Pus1 pseudouridine synthase 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20161222 MGI PMID:27197761 1323554 Pus1 pseudouridine synthase 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1323554 Pus1 pseudouridine synthase 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20161222 MGI PMID:27197761 1323554 Pus1 pseudouridine synthase 1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20161222 MGI PMID:27197761 1323554 Pus1 pseudouridine synthase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1323554 Pus1 pseudouridine synthase 1 gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20161222 MGI PMID:27197761 1323554 Pus1 pseudouridine synthase 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20161222 MGI PMID:27197761 1323556 Twf1 twinfilin actin binding protein 1 gene MP:0001191 abnormal skin condition IEA N RGD:5509061 20141003 MGI 1323556 Twf1 twinfilin actin binding protein 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1323556 Twf1 twinfilin actin binding protein 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1323558 Rec114 REC114 meiotic recombination protein gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0001925 male infertility IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0001926 female infertility IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20230420 MGI PMID:31000436 1323558 Rec114 REC114 meiotic recombination protein gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20190404 MGI PMID:30569039 1323558 Rec114 REC114 meiotic recombination protein gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:30569039 1323560 Cdc25c cell division cycle 25C gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21283624 1323560 Cdc25c cell division cycle 25C gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21283624 1323560 Cdc25c cell division cycle 25C gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21283624 1323560 Cdc25c cell division cycle 25C gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19273838 1323560 Cdc25c cell division cycle 25C gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19273838 1323560 Cdc25c cell division cycle 25C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11359894 1323560 Cdc25c cell division cycle 25C gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:19273838 1323560 Cdc25c cell division cycle 25C gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:21283624 1323560 Cdc25c cell division cycle 25C gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:19273838 1323560 Cdc25c cell division cycle 25C gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20141003 MGI PMID:21283624 1323560 Cdc25c cell division cycle 25C gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21283624 1323560 Cdc25c cell division cycle 25C gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21283624 1323560 Cdc25c cell division cycle 25C gene MP:0010159 abnormal enterocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:21283624 1323560 Cdc25c cell division cycle 25C gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21283624 1323560 Cdc25c cell division cycle 25C gene MP:0013958 decreased small intestine length IAGP N RGD:5509061 20160310 MGI PMID:19273838 1323560 Cdc25c cell division cycle 25C gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20160310 MGI PMID:19273838 1323561 Slc9b2 solute carrier family 9, subfamily B (NHA2, cation proton antiporter 2), member 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20231207 MGI 1323561 Slc9b2 solute carrier family 9, subfamily B (NHA2, cation proton antiporter 2), member 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23720317 1323561 Slc9b2 solute carrier family 9, subfamily B (NHA2, cation proton antiporter 2), member 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:23720317 1323561 Slc9b2 solute carrier family 9, subfamily B (NHA2, cation proton antiporter 2), member 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23720317 1323564 Actr8 ARP8 actin-related protein 8 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1323564 Actr8 ARP8 actin-related protein 8 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1323564 Actr8 ARP8 actin-related protein 8 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191128 MGI 1323564 Actr8 ARP8 actin-related protein 8 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191128 MGI 1323564 Actr8 ARP8 actin-related protein 8 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191128 MGI 1323564 Actr8 ARP8 actin-related protein 8 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1323564 Actr8 ARP8 actin-related protein 8 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1323564 Actr8 ARP8 actin-related protein 8 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1323564 Actr8 ARP8 actin-related protein 8 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191128 MGI 1323564 Actr8 ARP8 actin-related protein 8 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220519 MGI 1323564 Actr8 ARP8 actin-related protein 8 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191128 MGI 1323564 Actr8 ARP8 actin-related protein 8 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1323564 Actr8 ARP8 actin-related protein 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323564 Actr8 ARP8 actin-related protein 8 gene MP:0012724 absent head fold IEA N RGD:5509061 20191128 MGI 1323564 Actr8 ARP8 actin-related protein 8 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191128 MGI 1323570 Epx eosinophil peroxidase gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 1323570 Epx eosinophil peroxidase gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20181227 MGI 1323570 Epx eosinophil peroxidase gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23630390 1323570 Epx eosinophil peroxidase gene MP:0005061 abnormal eosinophil morphology IAGP N RGD:5509061 20141003 MGI PMID:11466391 1323570 Epx eosinophil peroxidase gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20150528 MGI PMID:25514040 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000445 short snout IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:19820125 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20150528 MGI PMID:25514040 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20171026 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0003053 delayed tooth eruption IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20150528 MGI PMID:25514040 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0003761 arched palate IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:19820125 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0004553 absent tracheal cartilage rings IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0004674 thin ribs IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0009900 vomer bone hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0010981 abnormal branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19820125 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:19820125 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12446778 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17997399 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:19820125 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0011425 abnormal kidney interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:19820125 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210520 MGI 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0030192 downturned snout IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0030259 mandibular condyloid process hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0030285 mandibular coronoid process hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0030377 zygomatic arch hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0030467 abnormal cranial cartilage development IAGP N RGD:5509061 20221110 MGI PMID:31130868 1323572 Trps1 transcriptional repressor GATA binding 1 gene MP:0031459 maxillary zygomatic process hypoplasia IAGP N RGD:5509061 20221201 MGI PMID:31130868 1323574 Iqgap1 IQ motif containing GTPase activating protein 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1323574 Iqgap1 IQ motif containing GTPase activating protein 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1323574 Iqgap1 IQ motif containing GTPase activating protein 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20221215 MGI 1323574 Iqgap1 IQ motif containing GTPase activating protein 1 gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 1323574 Iqgap1 IQ motif containing GTPase activating protein 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18180285 1323574 Iqgap1 IQ motif containing GTPase activating protein 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:18180285 1323574 Iqgap1 IQ motif containing GTPase activating protein 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1323574 Iqgap1 IQ motif containing GTPase activating protein 1 gene MP:0005210 disorganized stomach mucosa IAGP N RGD:5509061 20141003 MGI PMID:10611248 1323574 Iqgap1 IQ motif containing GTPase activating protein 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 1323574 Iqgap1 IQ motif containing GTPase activating protein 1 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10611248 1323578 Kif22 kinesin family member 22 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18329364 1323578 Kif22 kinesin family member 22 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18329364 1323578 Kif22 kinesin family member 22 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:18329364 1323578 Kif22 kinesin family member 22 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18329364 1323579 Ctif CBP80/20-dependent translation initiation factor gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1323579 Ctif CBP80/20-dependent translation initiation factor gene MP:0002626 increased heart rate IEA N RGD:5509061 20240523 MGI 1323579 Ctif CBP80/20-dependent translation initiation factor gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20221027 MGI 1323579 Ctif CBP80/20-dependent translation initiation factor gene MP:0010507 shortened RR interval IEA N RGD:5509061 20240523 MGI 1323581 Bivm basic, immunoglobulin-like variable motif containing gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1323581 Bivm basic, immunoglobulin-like variable motif containing gene MP:0013406 abnormal epidermal immune compartment IEA N RGD:5509061 20201231 MGI 1323584 Zfr zinc finger RNA binding protein gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:11283266 1323584 Zfr zinc finger RNA binding protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11283266 1323584 Zfr zinc finger RNA binding protein gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11283266 1323584 Zfr zinc finger RNA binding protein gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11283266 1323584 Zfr zinc finger RNA binding protein gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11283266 1323592 S100a11 S100 calcium binding protein A11 gene MP:0002673 abnormal sperm number IAGP N RGD:5509061 20141003 MGI PMID:14579419 1323599 Mfsd10 major facilitator superfamily domain containing 10 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1323601 Rhbdl3 rhomboid like 3 gene MP:0000745 tremors IEA N RGD:5509061 20181227 MGI 1323601 Rhbdl3 rhomboid like 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1323603 Slirp SRA stem-loop interacting RNA binding protein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23976951 1323603 Slirp SRA stem-loop interacting RNA binding protein gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20141003 MGI PMID:23976951 1323603 Slirp SRA stem-loop interacting RNA binding protein gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23976951 1323603 Slirp SRA stem-loop interacting RNA binding protein gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:23976951 1323603 Slirp SRA stem-loop interacting RNA binding protein gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220714 MGI PMID:23976951 1323605 Vgll2 vestigial like family member 2 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20190912 MGI PMID:28769032 1323605 Vgll2 vestigial like family member 2 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20190912 MGI PMID:28769032 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000601 small liver IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000746 weakness IEA N RGD:5509061 20141003 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000774 decreased brain size IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0001314 cornea opacity IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0001326 retina degeneration IEA N RGD:5509061 20141003 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0002772 brachypodia IAGP N RGD:5509061 20141003 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0002993 autoimmune arthritis IEA N RGD:5509061 20141003 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0004674 thin ribs IAGP N RGD:5509061 20141003 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0005114 premature hair loss IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20141003 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0008974 proportional dwarf IEA N RGD:5509061 20200430 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0009346 decreased trabecular bone thickness IEA N RGD:5509061 20141003 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20230119 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20141003 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20141003 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0010869 decreased bone trabecula number IEA N RGD:5509061 20141003 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0010879 decreased trabecular bone volume IEA N RGD:5509061 20141003 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0010933 decreased trabecular bone connectivity density IEA N RGD:5509061 20141003 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0013258 abnormal extracellular matrix morphology IAGP N RGD:5509061 20200514 MGI PMID:31754016 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0013616 decreased volumetric bone mineral density IEA N RGD:5509061 20150319 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0014106 delayed chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0020010 decreased bone mineral density of femur IEA N RGD:5509061 20220915 MGI 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0020138 delayed bone mineralization IAGP N RGD:5509061 20220915 MGI PMID:22280990 1323607 Chsy1 chondroitin sulfate synthase 1 gene MP:0021186 decreased bone mineral density of vertebrae IEA N RGD:5509061 20220915 MGI 1323618 Ccdc59 coiled-coil domain containing 59 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1323618 Ccdc59 coiled-coil domain containing 59 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191205 MGI 1323618 Ccdc59 coiled-coil domain containing 59 gene MP:0001694 absent egg cylinders IEA N RGD:5509061 20191205 MGI 1323618 Ccdc59 coiled-coil domain containing 59 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191205 MGI 1323618 Ccdc59 coiled-coil domain containing 59 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191205 MGI 1323618 Ccdc59 coiled-coil domain containing 59 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1323618 Ccdc59 coiled-coil domain containing 59 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1323618 Ccdc59 coiled-coil domain containing 59 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191205 MGI 1323618 Ccdc59 coiled-coil domain containing 59 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1323618 Ccdc59 coiled-coil domain containing 59 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323618 Ccdc59 coiled-coil domain containing 59 gene MP:0012724 absent head fold IEA N RGD:5509061 20191205 MGI 1323618 Ccdc59 coiled-coil domain containing 59 gene MP:0013241 embryo tissue necrosis IEA N RGD:5509061 20191205 MGI 1323618 Ccdc59 coiled-coil domain containing 59 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191205 MGI 1323620 Slc25a38 solute carrier family 25, member 38 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1323622 Flnb filamin, beta gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0000154 rib fusion IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:17635842 1323622 Flnb filamin, beta gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20150917 MGI PMID:23979929 1323622 Flnb filamin, beta gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17606870 1323622 Flnb filamin, beta gene MP:0000160 kyphosis IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:17635842 1323622 Flnb filamin, beta gene MP:0000161 scoliosis IAGP N RGD:5509061 20150917 MGI PMID:23979929 1323622 Flnb filamin, beta gene MP:0000161 scoliosis IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0000162 lordosis IAGP N RGD:5509061 20150917 MGI PMID:23979929 1323622 Flnb filamin, beta gene MP:0000162 lordosis IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17606870 1323622 Flnb filamin, beta gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20160310 MGI PMID:24551245 1323622 Flnb filamin, beta gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20181227 MGI 1323622 Flnb filamin, beta gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:17635842 1323622 Flnb filamin, beta gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0001255 decreased body height IAGP N RGD:5509061 20150917 MGI PMID:23979929 1323622 Flnb filamin, beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17635842 1323622 Flnb filamin, beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17606870 1323622 Flnb filamin, beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17635842 1323622 Flnb filamin, beta gene MP:0001406 abnormal gait IAGP N RGD:5509061 20150917 MGI PMID:23979929 1323622 Flnb filamin, beta gene MP:0001429 dehydration IAGP N RGD:5509061 20150917 MGI PMID:23979929 1323622 Flnb filamin, beta gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:17606870 1323622 Flnb filamin, beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:17606870 1323622 Flnb filamin, beta gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1323622 Flnb filamin, beta gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20160310 MGI PMID:24551245 1323622 Flnb filamin, beta gene MP:0003345 decreased rib number IAGP N RGD:5509061 20150917 MGI PMID:23979929 1323622 Flnb filamin, beta gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20160310 MGI PMID:24551245 1323622 Flnb filamin, beta gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0003410 abnormal artery development IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20160310 MGI PMID:24551245 1323622 Flnb filamin, beta gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160421 MGI 1323622 Flnb filamin, beta gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:17606870 1323622 Flnb filamin, beta gene MP:0004355 short radius IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0004355 short radius IAGP N RGD:5509061 20160310 MGI PMID:24551245 1323622 Flnb filamin, beta gene MP:0004441 small occipital bone IAGP N RGD:5509061 20141003 MGI PMID:17606870 1323622 Flnb filamin, beta gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:17635842 1323622 Flnb filamin, beta gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:17606870 1323622 Flnb filamin, beta gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20150917 MGI PMID:23979929 1323622 Flnb filamin, beta gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20150917 MGI PMID:23979929 1323622 Flnb filamin, beta gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0004674 thin ribs IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20160310 MGI PMID:24551245 1323622 Flnb filamin, beta gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:17635842 1323622 Flnb filamin, beta gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0005353 abnormal patella morphology IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0005426 tachypnea IAGP N RGD:5509061 20150917 MGI PMID:23979929 1323622 Flnb filamin, beta gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0006322 abnormal perichondrium morphology IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20160310 MGI PMID:24551245 1323622 Flnb filamin, beta gene MP:0006429 abnormal hyaline cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0008155 decreased diameter of radius IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0008157 decreased diameter of ulna IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17606870 1323622 Flnb filamin, beta gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17606870 1323622 Flnb filamin, beta gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:17606870 1323622 Flnb filamin, beta gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:17635842 1323622 Flnb filamin, beta gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20160310 MGI PMID:24551245 1323622 Flnb filamin, beta gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1323622 Flnb filamin, beta gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1323622 Flnb filamin, beta gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160421 MGI 1323622 Flnb filamin, beta gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17606870 1323622 Flnb filamin, beta gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17635842 1323622 Flnb filamin, beta gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17635842 1323622 Flnb filamin, beta gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323622 Flnb filamin, beta gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20150917 MGI PMID:23979929 1323622 Flnb filamin, beta gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0013258 abnormal extracellular matrix morphology IAGP N RGD:5509061 20151112 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0014289 decreased distal limb length IAGP N RGD:5509061 20230824 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0020487 abnormal middle cerebral artery morphology IAGP N RGD:5509061 20171026 MGI PMID:17360453 1323622 Flnb filamin, beta gene MP:0021186 decreased bone mineral density of vertebrae IAGP N RGD:5509061 20220915 MGI PMID:17510210 1323622 Flnb filamin, beta gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:17606870 1323622 Flnb filamin, beta gene MP:0030797 joint laxity IAGP N RGD:5509061 20181011 MGI PMID:17510210 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20240523 MGI 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0000371 diluted coat color IEA N RGD:5509061 20111116 MGI 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12548288 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20111116 MGI 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:6776948 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0002412 increased susceptibility to bacterial infection IEA N RGD:5509061 20111116 MGI 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:2369371 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:6696991 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20240523 MGI 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0005100 abnormal choroid pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12548288 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0005102 abnormal iris pigmentation IEA N RGD:5509061 20231207 MGI 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0005172 decreased eye pigmentation IEA N RGD:5509061 20111116 MGI 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20150416 MGI PMID:12548288 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:2369371 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0005408 hypopigmentation IEA N RGD:5509061 20180215 MGI 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:6696991 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0009379 abnormal foot pigmentation IEA N RGD:5509061 20111116 MGI 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20141003 MGI PMID:6696991 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0009557 decreased platelet ADP level IAGP N RGD:5509061 20141003 MGI PMID:6696991 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:6776948 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0011277 decreased tail pigmentation IEA N RGD:5509061 20111116 MGI 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0011279 decreased ear pigmentation IEA N RGD:5509061 20111116 MGI 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0011568 decreased foot pigmentation IEA N RGD:5509061 20150108 MGI 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0012122 abnormal iris transillumination IEA N RGD:5509061 20231207 MGI 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170720 MGI PMID:6696991 1323624 Hps5 HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 gene MP:0020916 increased susceptibility to Herpesvirales infection IEA N RGD:5509061 20200430 MGI 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230119 MGI 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0001574 abnormal oxygen level IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0004560 abnormal chorionic plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230119 MGI 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1323628 Ss18 SS18, subunit of BAF chromatin remodeling complex gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16926188 1323632 Ttll6 tubulin tyrosine ligase-like family, member 6 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170105 MGI 1323632 Ttll6 tubulin tyrosine ligase-like family, member 6 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20211021 MGI 1323633 Chd3 chromodomain helicase DNA binding protein 3 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1323633 Chd3 chromodomain helicase DNA binding protein 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1323633 Chd3 chromodomain helicase DNA binding protein 3 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20201015 MGI PMID:32658897 1323633 Chd3 chromodomain helicase DNA binding protein 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:32658897 1323633 Chd3 chromodomain helicase DNA binding protein 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20201015 MGI PMID:32658897 1323633 Chd3 chromodomain helicase DNA binding protein 3 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20201015 MGI PMID:32658897 1323636 Mcrip1 MAPK regulated corepressor interacting protein 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20190912 MGI PMID:31240265 1323636 Mcrip1 MAPK regulated corepressor interacting protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190912 MGI PMID:31240265 1323636 Mcrip1 MAPK regulated corepressor interacting protein 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20190912 MGI PMID:31240265 1323636 Mcrip1 MAPK regulated corepressor interacting protein 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20190912 MGI PMID:31240265 1323636 Mcrip1 MAPK regulated corepressor interacting protein 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20190912 MGI PMID:31240265 1323636 Mcrip1 MAPK regulated corepressor interacting protein 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20190912 MGI PMID:31240265 1323636 Mcrip1 MAPK regulated corepressor interacting protein 1 gene MP:0005426 tachypnea IAGP N RGD:5509061 20190912 MGI PMID:31240265 1323636 Mcrip1 MAPK regulated corepressor interacting protein 1 gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20190912 MGI PMID:31240265 1323636 Mcrip1 MAPK regulated corepressor interacting protein 1 gene MP:0010889 small alveolar lamellar bodies IAGP N RGD:5509061 20190912 MGI PMID:31240265 1323636 Mcrip1 MAPK regulated corepressor interacting protein 1 gene MP:0010890 decreased alveolar lamellar body number IAGP N RGD:5509061 20190912 MGI PMID:31240265 1323636 Mcrip1 MAPK regulated corepressor interacting protein 1 gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20190912 MGI PMID:31240265 1323636 Mcrip1 MAPK regulated corepressor interacting protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20190912 MGI PMID:31240265 1323636 Mcrip1 MAPK regulated corepressor interacting protein 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20190912 MGI PMID:31240265 1323636 Mcrip1 MAPK regulated corepressor interacting protein 1 gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20190912 MGI PMID:31240265 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20220324 MGI PMID:34942119 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20220324 MGI PMID:34942119 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20220324 MGI PMID:34942119 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220324 MGI PMID:34942119 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0001926 female infertility IEA N RGD:5509061 20220811 MGI 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220811 MGI 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220811 MGI 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220811 MGI 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1323638 Anapc7 anaphase promoting complex subunit 7 gene MP:0020421 increased freezing behavior IAGP N RGD:5509061 20220324 MGI PMID:34942119 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:17420276 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:17420276 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20668298 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:20668298 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:20668298 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17420276 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20668298 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20668298 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17420276 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:17420276 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17296732 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17296732 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20668298 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:17420276 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17296732 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17296732 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:17420276 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0002634 abnormal sensorimotor gating IAGP N RGD:5509061 20141003 MGI PMID:17420276 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0002895 abnormal otolithic membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17420276 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17420276 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17420276 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17296732 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:20668298 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:17420276 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:19103880 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:19103880 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:19103880 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:17296732 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17296732 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:17296732 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20668298 1323641 Cmah cytidine monophospho-N-acetylneuraminic acid hydroxylase gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:20668298 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20201022 MGI 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20170413 MGI PMID:25220394 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20170413 MGI PMID:27381259 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170413 MGI PMID:27381259 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170413 MGI PMID:27381259 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170413 MGI PMID:27381259 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20170413 MGI PMID:27381259 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20170413 MGI PMID:27381259 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:27381259 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20170413 MGI PMID:27381259 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160804 MGI 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20170413 MGI PMID:27381259 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20170413 MGI PMID:27381259 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20170413 MGI PMID:27381259 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20170413 MGI PMID:27381259 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141030 MGI PMID:24386439 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170413 MGI PMID:27381259 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20170413 MGI PMID:27381259 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20221215 MGI 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20170413 MGI PMID:25220394 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0011240 abnormal fetal derived definitive erythrocyte morphology IAGP N RGD:5509061 20170413 MGI PMID:25220394 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0011243 decreased fetal derived definitive erythrocyte cell number IAGP N RGD:5509061 20170413 MGI PMID:25220394 1323643 Cpeb4 cytoplasmic polyadenylation element binding protein 4 gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20170413 MGI PMID:27381259 1323648 Chd1l chromodomain helicase DNA binding protein 1-like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210401 MGI PMID:33333017 1323648 Chd1l chromodomain helicase DNA binding protein 1-like gene MP:0001265 decreased body size IAGP N RGD:5509061 20210401 MGI PMID:33333017 1323648 Chd1l chromodomain helicase DNA binding protein 1-like gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20210401 MGI PMID:33333017 1323648 Chd1l chromodomain helicase DNA binding protein 1-like gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20210401 MGI PMID:33333017 1323648 Chd1l chromodomain helicase DNA binding protein 1-like gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20210401 MGI PMID:33333017 1323648 Chd1l chromodomain helicase DNA binding protein 1-like gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210401 MGI PMID:33333017 1323648 Chd1l chromodomain helicase DNA binding protein 1-like gene MP:0011999 abnormal tail length IEA N RGD:5509061 20210826 MGI 1323650 Rnf20 ring finger protein 20 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1323650 Rnf20 ring finger protein 20 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1323650 Rnf20 ring finger protein 20 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0009310 increased large intestine adenocarcinoma incidence IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1323650 Rnf20 ring finger protein 20 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1323650 Rnf20 ring finger protein 20 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1323650 Rnf20 ring finger protein 20 gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20210722 MGI PMID:26854224 1323650 Rnf20 ring finger protein 20 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1323653 Bap1 Brca1 associated protein 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1323653 Bap1 Brca1 associated protein 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1323653 Bap1 Brca1 associated protein 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20170202 MGI PMID:26896281 1323653 Bap1 Brca1 associated protein 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20201231 MGI 1323653 Bap1 Brca1 associated protein 1 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1323653 Bap1 Brca1 associated protein 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20151022 MGI PMID:24928783 1323653 Bap1 Brca1 associated protein 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20151022 MGI PMID:24928783 1323653 Bap1 Brca1 associated protein 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20170202 MGI PMID:26896281 1323653 Bap1 Brca1 associated protein 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1323653 Bap1 Brca1 associated protein 1 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20170202 MGI PMID:26896281 1323653 Bap1 Brca1 associated protein 1 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20170202 MGI PMID:26896281 1323653 Bap1 Brca1 associated protein 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20151022 MGI PMID:24928783 1323653 Bap1 Brca1 associated protein 1 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20170202 MGI PMID:26896281 1323653 Bap1 Brca1 associated protein 1 gene MP:0010309 increased mesothelioma incidence IAGP N RGD:5509061 20170202 MGI PMID:26896281 1323653 Bap1 Brca1 associated protein 1 gene MP:0010348 increased pancreatic islet cell carcinoma incidence IAGP N RGD:5509061 20170202 MGI PMID:26896281 1323653 Bap1 Brca1 associated protein 1 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20151022 MGI PMID:24928783 1323653 Bap1 Brca1 associated protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1323653 Bap1 Brca1 associated protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323653 Bap1 Brca1 associated protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1323653 Bap1 Brca1 associated protein 1 gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20151022 MGI PMID:24928783 1323653 Bap1 Brca1 associated protein 1 gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20170202 MGI PMID:26896281 1323653 Bap1 Brca1 associated protein 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20170202 MGI PMID:26896281 1323653 Bap1 Brca1 associated protein 1 gene MP:0012436 increased colon tumor incidence IAGP N RGD:5509061 20170202 MGI PMID:26896281 1323653 Bap1 Brca1 associated protein 1 gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20161124 MGI PMID:22878500 1323653 Bap1 Brca1 associated protein 1 gene MP:0030025 giant platelets IAGP N RGD:5509061 20170803 MGI PMID:22878500 1323658 Asf1a anti-silencing function 1A histone chaperone gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1323658 Asf1a anti-silencing function 1A histone chaperone gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20160811 MGI 1323658 Asf1a anti-silencing function 1A histone chaperone gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1323658 Asf1a anti-silencing function 1A histone chaperone gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20160811 MGI 1323658 Asf1a anti-silencing function 1A histone chaperone gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1323658 Asf1a anti-silencing function 1A histone chaperone gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20160811 MGI 1323658 Asf1a anti-silencing function 1A histone chaperone gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1323658 Asf1a anti-silencing function 1A histone chaperone gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21987787 1323658 Asf1a anti-silencing function 1A histone chaperone gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323658 Asf1a anti-silencing function 1A histone chaperone gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1323658 Asf1a anti-silencing function 1A histone chaperone gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1323661 Nans N-acetylneuraminic acid synthase (sialic acid synthase) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1323661 Nans N-acetylneuraminic acid synthase (sialic acid synthase) gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220519 MGI 1323661 Nans N-acetylneuraminic acid synthase (sialic acid synthase) gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1323661 Nans N-acetylneuraminic acid synthase (sialic acid synthase) gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1323661 Nans N-acetylneuraminic acid synthase (sialic acid synthase) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 1323661 Nans N-acetylneuraminic acid synthase (sialic acid synthase) gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1323661 Nans N-acetylneuraminic acid synthase (sialic acid synthase) gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20210128 MGI 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0004222 iris synechia IEA N RGD:5509061 20190502 MGI 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0010187 decreased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:23997217 1323662 Itfg2 integrin alpha FG-GAP repeat containing 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1323666 1810055G02Rik RIKEN cDNA 1810055G02 gene gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20240523 MGI 1323668 Npat nuclear protein in the AT region gene MP:0000154 rib fusion IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0000297 abnormal atrioventricular cushion morphology IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0004201 fetal growth retardation IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0008923 thoracoschisis IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20200310 MGI PMID:9199343 1323668 Npat nuclear protein in the AT region gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9199343 1323668 Npat nuclear protein in the AT region gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323668 Npat nuclear protein in the AT region gene MP:0011493 double ureter IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0012111 failure of morula compaction IAGP N RGD:5509061 20200310 MGI PMID:9199343 1323668 Npat nuclear protein in the AT region gene MP:0013815 abnormal digastric muscle morphology IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0013943 abnormal ureter topology IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0013966 abnormal infrahyoid muscle morphology IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0013968 multiple persisting craniopharyngeal ducts IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0013977 symmetric azygos veins IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0013996 abnormal vertebral artery origin IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0014023 abnormal intestine placement IEA N RGD:5509061 20170504 MGI 1323668 Npat nuclear protein in the AT region gene MP:0014087 retrolental blood IEA N RGD:5509061 20180628 MGI 1323668 Npat nuclear protein in the AT region gene MP:0020500 persistent trigeminal artery IEA N RGD:5509061 20180628 MGI 1323672 Sphkap SPHK1 interactor, AKAP domain containing gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20201210 MGI PMID:28396589 1323672 Sphkap SPHK1 interactor, AKAP domain containing gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20201210 MGI PMID:28396589 1323672 Sphkap SPHK1 interactor, AKAP domain containing gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20201210 MGI PMID:28396589 1323672 Sphkap SPHK1 interactor, AKAP domain containing gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20201210 MGI PMID:28396589 1323672 Sphkap SPHK1 interactor, AKAP domain containing gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20201210 MGI PMID:28396589 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17657313 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:22851711 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16449664 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17657313 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:22851711 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:22851711 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17657313 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:16449664 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:16449664 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0005000 abnormal immune tolerance IAGP N RGD:5509061 20141003 MGI PMID:17657313 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0005630 increased lung weight IEA N RGD:5509061 20211021 MGI 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16449664 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:16449664 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16449664 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0008240 abnormal spleen marginal zone macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:17657313 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0008241 abnormal metallophilic macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:17657313 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22851711 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22851711 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:22851711 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:22851711 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:22851711 1323675 Siglec1 sialic acid binding Ig-like lectin 1, sialoadhesin gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:22851711 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20150924 MGI PMID:25255451 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16107704 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20150924 MGI PMID:25255451 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20150924 MGI PMID:25255451 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:15205536 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20150924 MGI PMID:25255451 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0001861 lung inflammation IAGP N RGD:5509061 20150924 MGI PMID:25255451 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0001958 emphysema IAGP N RGD:5509061 20150924 MGI PMID:25255451 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15205536 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15205536 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15205536 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0003395 abnormal subclavian artery morphology IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:15205536 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0004044 aortic dissection IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0006265 increased pulse pressure IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:24076219 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20150924 MGI PMID:25255451 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0008775 abnormal heart ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20170608 MGI PMID:26980189 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:24076219 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15205536 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16107704 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20150924 MGI PMID:25255451 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0009871 abnormal aorta tunica adventitia morphology IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20150924 MGI PMID:25255451 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15205536 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0010468 abnormal thoracic aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0010470 dilated ascending aorta IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0010661 ascending aorta aneurysm IAGP N RGD:5509061 20150924 MGI PMID:25255451 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:17293478 1323680 Mus81 MUS81 structure-specific endonuclease subunit gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15205536 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20201022 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210826 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20201022 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20230601 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210520 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0009084 blind uterus IEA N RGD:5509061 20210826 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323688 Pole2 polymerase (DNA directed), epsilon 2 (p59 subunit) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1323691 Rbbp6 retinoblastoma binding protein 6, ubiquitin ligase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17470788 1323691 Rbbp6 retinoblastoma binding protein 6, ubiquitin ligase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17470788 1323691 Rbbp6 retinoblastoma binding protein 6, ubiquitin ligase gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17470788 1323691 Rbbp6 retinoblastoma binding protein 6, ubiquitin ligase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17470788 1323691 Rbbp6 retinoblastoma binding protein 6, ubiquitin ligase gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17470788 1323693 Galnt12 polypeptide N-acetylgalactosaminyltransferase 12 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1323693 Galnt12 polypeptide N-acetylgalactosaminyltransferase 12 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1323699 B3gat3 beta-1,3-glucuronyltransferase 3 gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 1323699 B3gat3 beta-1,3-glucuronyltransferase 3 gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 1323699 B3gat3 beta-1,3-glucuronyltransferase 3 gene MP:0006204 embryonic lethality before implantation IAGP N RGD:5509061 20151217 MGI PMID:20164174 1323699 B3gat3 beta-1,3-glucuronyltransferase 3 gene MP:0011475 abnormal glycosaminoglycan level IAGP N RGD:5509061 20151217 MGI PMID:20164174 1323699 B3gat3 beta-1,3-glucuronyltransferase 3 gene MP:0013289 abnormal mitotic cytokinesis IAGP N RGD:5509061 20151217 MGI PMID:20164174 1323701 Car6 carbonic anhydrase 6 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1323701 Car6 carbonic anhydrase 6 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1323701 Car6 carbonic anhydrase 6 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1323701 Car6 carbonic anhydrase 6 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1323701 Car6 carbonic anhydrase 6 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1323701 Car6 carbonic anhydrase 6 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1323701 Car6 carbonic anhydrase 6 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1323701 Car6 carbonic anhydrase 6 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1323701 Car6 carbonic anhydrase 6 gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20835760 1323701 Car6 carbonic anhydrase 6 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20231207 MGI 1323701 Car6 carbonic anhydrase 6 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20230601 MGI 1323701 Car6 carbonic anhydrase 6 gene MP:0011045 decreased lung elastance IEA N RGD:5509061 20230601 MGI 1323701 Car6 carbonic anhydrase 6 gene MP:0013129 abnormal tooth color IEA N RGD:5509061 20230601 MGI 1323702 Zc2hc1a zinc finger, C2HC-type containing 1A gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1323702 Zc2hc1a zinc finger, C2HC-type containing 1A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1323702 Zc2hc1a zinc finger, C2HC-type containing 1A gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1323702 Zc2hc1a zinc finger, C2HC-type containing 1A gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20211021 MGI 1323704 Uqcrb ubiquinol-cytochrome c reductase binding protein gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1323704 Uqcrb ubiquinol-cytochrome c reductase binding protein gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1323704 Uqcrb ubiquinol-cytochrome c reductase binding protein gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1323704 Uqcrb ubiquinol-cytochrome c reductase binding protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:9501099 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:9501099 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:9501099 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:9501099 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9501099 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:15738389 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9087432 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:9087432 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12968018 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9501099 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15738389 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:9087432 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15738389 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:18826952 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20161103 MGI PMID:25041126 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:15738389 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18826952 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15738389 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15738389 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15738389 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:12968018 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:9501099 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12968018 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9501099 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18826952 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20161103 MGI PMID:25041126 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12968018 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:12968018 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9501099 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9501099 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12968018 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20161103 MGI PMID:18826952 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9087432 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9501099 1323706 Nfe2l1 nuclear factor, erythroid derived 2,-like 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:12968018 1323710 Usp38 ubiquitin specific peptidase 38 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20181227 MGI 1323710 Usp38 ubiquitin specific peptidase 38 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1323710 Usp38 ubiquitin specific peptidase 38 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20220407 MGI PMID:35238669 1323710 Usp38 ubiquitin specific peptidase 38 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1323710 Usp38 ubiquitin specific peptidase 38 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20160421 MGI 1323710 Usp38 ubiquitin specific peptidase 38 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1323710 Usp38 ubiquitin specific peptidase 38 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160421 MGI 1323710 Usp38 ubiquitin specific peptidase 38 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1323710 Usp38 ubiquitin specific peptidase 38 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20220407 MGI PMID:35238669 1323710 Usp38 ubiquitin specific peptidase 38 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20220407 MGI PMID:35238669 1323710 Usp38 ubiquitin specific peptidase 38 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1323710 Usp38 ubiquitin specific peptidase 38 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20220407 MGI PMID:35238669 1323710 Usp38 ubiquitin specific peptidase 38 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20160421 MGI 1323710 Usp38 ubiquitin specific peptidase 38 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1323717 Nbea neurobeachin gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1323717 Nbea neurobeachin gene MP:0000111 cleft palate IEA N RGD:5509061 20230601 MGI 1323717 Nbea neurobeachin gene MP:0000738 impaired muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15071111 1323717 Nbea neurobeachin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23153818 1323717 Nbea neurobeachin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15071111 1323717 Nbea neurobeachin gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:23153818 1323717 Nbea neurobeachin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23153818 1323717 Nbea neurobeachin gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:15071111 1323717 Nbea neurobeachin gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:19723784 1323717 Nbea neurobeachin gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:23153818 1323717 Nbea neurobeachin gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:23153818 1323717 Nbea neurobeachin gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:15071111 1323717 Nbea neurobeachin gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:19723784 1323717 Nbea neurobeachin gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15071111 1323717 Nbea neurobeachin gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19723784 1323717 Nbea neurobeachin gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 1323717 Nbea neurobeachin gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:23153818 1323717 Nbea neurobeachin gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:19723784 1323717 Nbea neurobeachin gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:23153818 1323717 Nbea neurobeachin gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19723784 1323717 Nbea neurobeachin gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:23153818 1323717 Nbea neurobeachin gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20230601 MGI 1323717 Nbea neurobeachin gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141003 MGI PMID:15071111 1323717 Nbea neurobeachin gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20231207 MGI 1323717 Nbea neurobeachin gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19723784 1323717 Nbea neurobeachin gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:19723784 1323717 Nbea neurobeachin gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:15071111 1323717 Nbea neurobeachin gene MP:0006320 abnormal interscapular fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15071111 1323717 Nbea neurobeachin gene MP:0006320 abnormal interscapular fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:19723784 1323717 Nbea neurobeachin gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19723784 1323717 Nbea neurobeachin gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23153818 1323717 Nbea neurobeachin gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:19723784 1323717 Nbea neurobeachin gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20231207 MGI 1323717 Nbea neurobeachin gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 1323717 Nbea neurobeachin gene MP:0010146 umbilical hernia IAGP N RGD:5509061 20141003 MGI PMID:19723784 1323717 Nbea neurobeachin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15071111 1323717 Nbea neurobeachin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19723784 1323717 Nbea neurobeachin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20221215 MGI 1323717 Nbea neurobeachin gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:19723784 1323717 Nbea neurobeachin gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:19723784 1323717 Nbea neurobeachin gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:19723784 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20160414 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20160414 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0001255 decreased body height IAGP N RGD:5509061 20160414 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0001348 abnormal lacrimal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0002819 abnormal dental pulp cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0003404 absent enamel IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0003668 abnormal periodontal ligament morphology IAGP N RGD:5509061 20160414 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0003930 abnormal tooth hard tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0003933 abnormal cementum morphology IAGP N RGD:5509061 20160414 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0006402 small molars IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20160414 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0009445 osteomalacia IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0010870 absent bone trabeculae IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20160414 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0011498 abnormal glomerular capsule parietal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0011504 abnormal limb long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0012175 flat face IAGP N RGD:5509061 20141003 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0013251 dental pulp necrosis IAGP N RGD:5509061 20171221 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0014104 decreased chondrocyte apoptosis IAGP N RGD:5509061 20171221 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:22615579 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20160414 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030132 periodontium inflammation IAGP N RGD:5509061 20171005 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030153 dental pulp inflammation IAGP N RGD:5509061 20171005 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030223 mandibular hyperostosis IAGP N RGD:5509061 20171019 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030462 tooth abscess IAGP N RGD:5509061 20171221 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030463 apical tooth abscess IAGP N RGD:5509061 20171221 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030466 alveolar process atrophy IAGP N RGD:5509061 20171221 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030484 abnormal osteocyte lacuna morphology IAGP N RGD:5509061 20171221 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030485 abnormal osteocyte lacunocanalicular system morphology IAGP N RGD:5509061 20171221 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030486 abnormal osteocyte canaliculus morphology IAGP N RGD:5509061 20171221 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030487 abnormal osteocyte dendritic process morphology IAGP N RGD:5509061 20171221 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030490 periodontal pocket IAGP N RGD:5509061 20171228 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030493 abnormal tooth root morphology IAGP N RGD:5509061 20171228 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030500 conical molar IAGP N RGD:5509061 20180125 MGI PMID:22732358 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030515 periodontal ligament necrosis IAGP N RGD:5509061 20180111 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030517 detached junctional epithelium IAGP N RGD:5509061 20180111 MGI PMID:25479552 1323720 Fam20c FAM20C, golgi associated secretory pathway kinase gene MP:0030542 abnormal dentin development IAGP N RGD:5509061 20180215 MGI PMID:22732358 1323723 Slc25a24 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20211118 MGI PMID:25599384 1323723 Slc25a24 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 1323723 Slc25a24 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20211118 MGI PMID:25599384 1323723 Slc25a24 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20211118 MGI PMID:25599384 1323723 Slc25a24 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20211118 MGI PMID:25599384 1323723 Slc25a24 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1323723 Slc25a24 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1323725 Rgma repulsive guidance molecule family member A gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:14749425 1323725 Rgma repulsive guidance molecule family member A gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:14749425 1323725 Rgma repulsive guidance molecule family member A gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:14749425 1323725 Rgma repulsive guidance molecule family member A gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:14749425 1323725 Rgma repulsive guidance molecule family member A gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:14749425 1323725 Rgma repulsive guidance molecule family member A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14749425 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16880528 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14645530 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23554489 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:23554489 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:23554489 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:22492726 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:23554489 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:23554489 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:16880528 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:16880528 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:23554489 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:23554489 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:23554489 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:23554489 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23554489 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16880528 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22492726 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0011707 impaired fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:22492726 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:23554489 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:23554489 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20170223 MGI PMID:22492726 1323729 Arpc3 actin related protein 2/3 complex, subunit 3 gene MP:0020415 abnormal fibroblast chemotaxis IAGP N RGD:5509061 20170223 MGI PMID:22492726 1323731 Ptgdr2 prostaglandin D2 receptor 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23624557 1323731 Ptgdr2 prostaglandin D2 receptor 2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16888024 1323731 Ptgdr2 prostaglandin D2 receptor 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16888024 1323731 Ptgdr2 prostaglandin D2 receptor 2 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16888024 1323731 Ptgdr2 prostaglandin D2 receptor 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16081770 1323731 Ptgdr2 prostaglandin D2 receptor 2 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16081770 1323731 Ptgdr2 prostaglandin D2 receptor 2 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23624557 1323731 Ptgdr2 prostaglandin D2 receptor 2 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:16888024 1323731 Ptgdr2 prostaglandin D2 receptor 2 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:16888024 1323731 Ptgdr2 prostaglandin D2 receptor 2 gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18097056 1323731 Ptgdr2 prostaglandin D2 receptor 2 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:16888024 1323732 Pld6 phospholipase D family member 6 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21397847 1323732 Pld6 phospholipase D family member 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21397847 1323732 Pld6 phospholipase D family member 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21397848 1323732 Pld6 phospholipase D family member 6 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21397848 1323732 Pld6 phospholipase D family member 6 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:21397848 1323732 Pld6 phospholipase D family member 6 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20141003 MGI PMID:21397847 1323732 Pld6 phospholipase D family member 6 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:21397847 1323732 Pld6 phospholipase D family member 6 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:21397848 1323732 Pld6 phospholipase D family member 6 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21397847 1323732 Pld6 phospholipase D family member 6 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21397847 1323732 Pld6 phospholipase D family member 6 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21397848 1323732 Pld6 phospholipase D family member 6 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:21397847 1323732 Pld6 phospholipase D family member 6 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21397847 1323732 Pld6 phospholipase D family member 6 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21397848 1323732 Pld6 phospholipase D family member 6 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21397847 1323732 Pld6 phospholipase D family member 6 gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:21397847 1323734 Fam83b family with sequence similarity 83, member B gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1323734 Fam83b family with sequence similarity 83, member B gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1323734 Fam83b family with sequence similarity 83, member B gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1323734 Fam83b family with sequence similarity 83, member B gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 1323734 Fam83b family with sequence similarity 83, member B gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1323734 Fam83b family with sequence similarity 83, member B gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1323734 Fam83b family with sequence similarity 83, member B gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1323734 Fam83b family with sequence similarity 83, member B gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 1323736 Ckap4 cytoskeleton-associated protein 4 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1323736 Ckap4 cytoskeleton-associated protein 4 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1323736 Ckap4 cytoskeleton-associated protein 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1323737 Ap4s1 adaptor-related protein complex AP-4, sigma 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20240523 MGI 1323739 Erf Ets2 repressor factor gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23354439 1323739 Erf Ets2 repressor factor gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:23354439 1323739 Erf Ets2 repressor factor gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1323739 Erf Ets2 repressor factor gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1323739 Erf Ets2 repressor factor gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:23354439 1323739 Erf Ets2 repressor factor gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20181227 MGI 1323739 Erf Ets2 repressor factor gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1323739 Erf Ets2 repressor factor gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190808 MGI 1323739 Erf Ets2 repressor factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20220811 MGI 1323739 Erf Ets2 repressor factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23354439 1323739 Erf Ets2 repressor factor gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1323739 Erf Ets2 repressor factor gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20181227 MGI 1323739 Erf Ets2 repressor factor gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1323739 Erf Ets2 repressor factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323739 Erf Ets2 repressor factor gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0012090 midbrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0012134 absent umbilical cord IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0012264 hindbrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17502352 1323739 Erf Ets2 repressor factor gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1323741 Mroh4 maestro heat-like repeat family member 4 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201022 MGI 1323742 Sowahb sosondowah ankyrin repeat domain family member B gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22384391 1323742 Sowahb sosondowah ankyrin repeat domain family member B gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:22384391 1323742 Sowahb sosondowah ankyrin repeat domain family member B gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:22384391 1323744 Zscan2 zinc finger and SCAN domain containing 2 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20201231 MGI 1323746 Ccl21a C-C motif chemokine ligand 21 (serine) gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20180426 MGI PMID:28611158 1323746 Ccl21a C-C motif chemokine ligand 21 (serine) gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20180426 MGI PMID:28611158 1323746 Ccl21a C-C motif chemokine ligand 21 (serine) gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20180426 MGI PMID:28611158 1323746 Ccl21a C-C motif chemokine ligand 21 (serine) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180426 MGI PMID:28611158 1323746 Ccl21a C-C motif chemokine ligand 21 (serine) gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20180426 MGI PMID:28611158 1323746 Ccl21a C-C motif chemokine ligand 21 (serine) gene MP:0012765 decreased alpha-beta T cell number IAGP N RGD:5509061 20180426 MGI PMID:28611158 1323746 Ccl21a C-C motif chemokine ligand 21 (serine) gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20180426 MGI PMID:28611158 1323746 Ccl21a C-C motif chemokine ligand 21 (serine) gene MP:0020220 decreased tear production IAGP N RGD:5509061 20180426 MGI PMID:28611158 1323752 Asph aspartate-beta-hydroxylase gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:11773073 1323752 Asph aspartate-beta-hydroxylase gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:11773073 1323752 Asph aspartate-beta-hydroxylase gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:11773073 1323752 Asph aspartate-beta-hydroxylase gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:17224479 1323752 Asph aspartate-beta-hydroxylase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11773073 1323752 Asph aspartate-beta-hydroxylase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11773073 1323752 Asph aspartate-beta-hydroxylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11773073 1323752 Asph aspartate-beta-hydroxylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17224479 1323752 Asph aspartate-beta-hydroxylase gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:17224479 1323752 Asph aspartate-beta-hydroxylase gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:17224479 1323752 Asph aspartate-beta-hydroxylase gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17224479 1323752 Asph aspartate-beta-hydroxylase gene MP:0006141 abnormal atrioventricular node conduction IAGP N RGD:5509061 20141003 MGI PMID:17224479 1323752 Asph aspartate-beta-hydroxylase gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:17224479 1323752 Asph aspartate-beta-hydroxylase gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11773073 1323754 Rdh11 retinol dehydrogenase 11 gene MP:0003011 delayed dark adaptation IAGP N RGD:5509061 20141003 MGI PMID:15634683 1323754 Rdh11 retinol dehydrogenase 11 gene MP:0003011 delayed dark adaptation IAGP N RGD:5509061 20141003 MGI PMID:15790565 1323754 Rdh11 retinol dehydrogenase 11 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15634683 1323756 Cobl cordon-bleu WH2 repeat gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240523 MGI 1323756 Cobl cordon-bleu WH2 repeat gene MP:0000274 enlarged heart IEA N RGD:5509061 20240523 MGI 1323756 Cobl cordon-bleu WH2 repeat gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 1323756 Cobl cordon-bleu WH2 repeat gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 1323756 Cobl cordon-bleu WH2 repeat gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:14512015 1323756 Cobl cordon-bleu WH2 repeat gene MP:0001935 decreased litter size IAGP N RGD:5509061 20221020 MGI PMID:30157434 1323756 Cobl cordon-bleu WH2 repeat gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7586755 1323756 Cobl cordon-bleu WH2 repeat gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20221020 MGI PMID:30157434 1323756 Cobl cordon-bleu WH2 repeat gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20221020 MGI PMID:30157434 1323756 Cobl cordon-bleu WH2 repeat gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20221020 MGI PMID:30157434 1323756 Cobl cordon-bleu WH2 repeat gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20221020 MGI PMID:30157434 1323756 Cobl cordon-bleu WH2 repeat gene MP:0011062 abnormal outer hair cell kinocilium morphology IAGP N RGD:5509061 20221020 MGI PMID:30157434 1323756 Cobl cordon-bleu WH2 repeat gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20221020 MGI PMID:30157434 1323756 Cobl cordon-bleu WH2 repeat gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20240523 MGI 1323756 Cobl cordon-bleu WH2 repeat gene MP:0030944 abnormal pericentriolar material morphology IAGP N RGD:5509061 20221020 MGI PMID:30157434 1323757 Alg14 asparagine-linked glycosylation 14 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20191205 MGI 1323757 Alg14 asparagine-linked glycosylation 14 gene MP:0008527 embryonic lethality at implantation IEA N RGD:5509061 20241017 MGI 1323757 Alg14 asparagine-linked glycosylation 14 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323757 Alg14 asparagine-linked glycosylation 14 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20240523 MGI 1323757 Alg14 asparagine-linked glycosylation 14 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20181227 MGI 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20181227 MGI 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210128 MGI PMID:32954300 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20210128 MGI PMID:32954300 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20210128 MGI PMID:32954300 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20210128 MGI PMID:32954300 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20210128 MGI PMID:32954300 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20210128 MGI PMID:32954300 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20181227 MGI 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20210128 MGI PMID:32954300 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20181227 MGI 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20181227 MGI 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20210128 MGI PMID:32954300 1323760 Minar2 membrane integral NOTCH2 associated receptor 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 1323763 Etv1 ets variant 1 gene MP:0000959 abnormal somatic sensory system morphology IAGP N RGD:5509061 20141003 MGI PMID:16493690 1323763 Etv1 ets variant 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11891988 1323763 Etv1 ets variant 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16493690 1323763 Etv1 ets variant 1 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:23522042 1323763 Etv1 ets variant 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:10850491 1323763 Etv1 ets variant 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:11891988 1323763 Etv1 ets variant 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15836427 1323763 Etv1 ets variant 1 gene MP:0000988 abnormal pacinian corpuscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16493690 1323763 Etv1 ets variant 1 gene MP:0000999 abnormal golgi tendon organ morphology IAGP N RGD:5509061 20141003 MGI PMID:11891988 1323763 Etv1 ets variant 1 gene MP:0001000 absent golgi tendon organ IAGP N RGD:5509061 20141003 MGI PMID:11891988 1323763 Etv1 ets variant 1 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:11891988 1323763 Etv1 ets variant 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11891988 1323763 Etv1 ets variant 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10850491 1323763 Etv1 ets variant 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:10850491 1323763 Etv1 ets variant 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10850491 1323763 Etv1 ets variant 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1323763 Etv1 ets variant 1 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:10850491 1323763 Etv1 ets variant 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:23522042 1323763 Etv1 ets variant 1 gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:11891988 1323763 Etv1 ets variant 1 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:10850491 1323763 Etv1 ets variant 1 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:11891988 1323763 Etv1 ets variant 1 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12741988 1323763 Etv1 ets variant 1 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23522042 1323763 Etv1 ets variant 1 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:10850491 1323763 Etv1 ets variant 1 gene MP:0006006 increased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:23522042 1323763 Etv1 ets variant 1 gene MP:0008468 absent muscle spindles IAGP N RGD:5509061 20141003 MGI PMID:11891988 1323763 Etv1 ets variant 1 gene MP:0008485 increased muscle spindle number IAGP N RGD:5509061 20141003 MGI PMID:11891988 1323763 Etv1 ets variant 1 gene MP:0008486 decreased muscle spindle number IAGP N RGD:5509061 20141003 MGI PMID:23522042 1323763 Etv1 ets variant 1 gene MP:0030996 decreased pacinian corpuscle number IAGP N RGD:5509061 20200130 MGI PMID:16493690 1323763 Etv1 ets variant 1 gene MP:0030998 small pacinian corpuscles IAGP N RGD:5509061 20200130 MGI PMID:16493690 1323765 Axl AXL receptor tyrosine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20170209 MGI PMID:18787040 1323765 Axl AXL receptor tyrosine kinase gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20170209 MGI PMID:18393392 1323765 Axl AXL receptor tyrosine kinase gene MP:0001144 vagina atresia IAGP N RGD:5509061 20170209 MGI PMID:18393392 1323765 Axl AXL receptor tyrosine kinase gene MP:0001147 small testis IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0001212 skin lesions IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0001925 male infertility IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20170209 MGI PMID:18787040 1323765 Axl AXL receptor tyrosine kinase gene MP:0002001 blindness IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170209 MGI 1323765 Axl AXL receptor tyrosine kinase gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0002425 abnormal susceptibility to autoimmune disorder IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0002933 joint inflammation IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20170209 MGI PMID:19729839 1323765 Axl AXL receptor tyrosine kinase gene MP:0003103 liver degeneration IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20170209 MGI PMID:18787040 1323765 Axl AXL receptor tyrosine kinase gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20170209 MGI PMID:18787040 1323765 Axl AXL receptor tyrosine kinase gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20170209 MGI PMID:18393392 1323765 Axl AXL receptor tyrosine kinase gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0005159 azoospermia IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20170209 MGI PMID:18787040 1323765 Axl AXL receptor tyrosine kinase gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20170209 MGI PMID:18787040 1323765 Axl AXL receptor tyrosine kinase gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20201119 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20170209 MGI PMID:11452127 1323765 Axl AXL receptor tyrosine kinase gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20170209 MGI PMID:18787040 1323765 Axl AXL receptor tyrosine kinase gene MP:0009008 delayed estrous cycle IAGP N RGD:5509061 20170209 MGI PMID:18787040 1323765 Axl AXL receptor tyrosine kinase gene MP:0009012 short diestrus IAGP N RGD:5509061 20170209 MGI PMID:18787040 1323765 Axl AXL receptor tyrosine kinase gene MP:0009014 prolonged proestrus IAGP N RGD:5509061 20170209 MGI PMID:18787040 1323765 Axl AXL receptor tyrosine kinase gene MP:0009322 increased splenocyte apoptosis IAGP N RGD:5509061 20201119 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0009396 small endometrial glands IAGP N RGD:5509061 20170209 MGI PMID:18393392 1323765 Axl AXL receptor tyrosine kinase gene MP:0009853 decreased Sertoli cell phagocytosis IAGP N RGD:5509061 20170209 MGI PMID:18159085 1323765 Axl AXL receptor tyrosine kinase gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20170209 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20201119 MGI PMID:10227296 1323765 Axl AXL receptor tyrosine kinase gene MP:0031168 abnormal brain thrombosis IAGP N RGD:5509061 20201119 MGI PMID:11452127 1323767 Pak5 p21 (RAC1) activated kinase 5 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1323767 Pak5 p21 (RAC1) activated kinase 5 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18675265 1323767 Pak5 p21 (RAC1) activated kinase 5 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:18675265 1323767 Pak5 p21 (RAC1) activated kinase 5 gene MP:0001513 limb grasping IEA N RGD:5509061 20210128 MGI 1323767 Pak5 p21 (RAC1) activated kinase 5 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1323767 Pak5 p21 (RAC1) activated kinase 5 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1323767 Pak5 p21 (RAC1) activated kinase 5 gene MP:0002798 abnormal active avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:18675265 1323767 Pak5 p21 (RAC1) activated kinase 5 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18675265 1323767 Pak5 p21 (RAC1) activated kinase 5 gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:18675265 1323767 Pak5 p21 (RAC1) activated kinase 5 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:18675265 1323767 Pak5 p21 (RAC1) activated kinase 5 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:18675265 1323767 Pak5 p21 (RAC1) activated kinase 5 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:18675265 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20200109 MGI PMID:31024568 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20200109 MGI PMID:31024568 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20200109 MGI PMID:31024568 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20200109 MGI PMID:31024568 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20200109 MGI PMID:31024568 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20200109 MGI PMID:31024568 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0013667 increased immature NK cell number IAGP N RGD:5509061 20200109 MGI PMID:31024568 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0013672 decreased mature NK cell number IAGP N RGD:5509061 20200109 MGI PMID:31024568 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0013699 abnormal immature NK cell morphology IAGP N RGD:5509061 20200109 MGI PMID:31024568 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:31024568 1323769 Kctd9 potassium channel tetramerisation domain containing 9 gene MP:0031047 decreased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:31024568 1323771 Shmt1 serine hydroxymethyltransferase 1 (soluble) gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:18644786 1323771 Shmt1 serine hydroxymethyltransferase 1 (soluble) gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1323771 Shmt1 serine hydroxymethyltransferase 1 (soluble) gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22438825 1323771 Shmt1 serine hydroxymethyltransferase 1 (soluble) gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1323771 Shmt1 serine hydroxymethyltransferase 1 (soluble) gene MP:0030625 increased circulating cysteine level IAGP N RGD:5509061 20180920 MGI PMID:18644786 1323771 Shmt1 serine hydroxymethyltransferase 1 (soluble) gene MP:0030688 decreased circulating cystathionine level IAGP N RGD:5509061 20180920 MGI PMID:18644786 1323773 Sprr1b small proline-rich protein 1B gene MP:0011471 decreased urine creatinine level IEA N RGD:5509061 20210128 MGI 1323775 Nt5c3 5'-nucleotidase, cytosolic III gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20230119 MGI 1323775 Nt5c3 5'-nucleotidase, cytosolic III gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1323775 Nt5c3 5'-nucleotidase, cytosolic III gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20231207 MGI 1323775 Nt5c3 5'-nucleotidase, cytosolic III gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1323775 Nt5c3 5'-nucleotidase, cytosolic III gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1323775 Nt5c3 5'-nucleotidase, cytosolic III gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1323775 Nt5c3 5'-nucleotidase, cytosolic III gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1323778 Xpo4 exportin 4 gene MP:0001147 small testis IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323778 Xpo4 exportin 4 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230119 MGI 1323778 Xpo4 exportin 4 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1323778 Xpo4 exportin 4 gene MP:0001785 edema IEA N RGD:5509061 20230119 MGI 1323778 Xpo4 exportin 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323778 Xpo4 exportin 4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20240314 MGI 1323778 Xpo4 exportin 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323778 Xpo4 exportin 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323778 Xpo4 exportin 4 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323778 Xpo4 exportin 4 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323778 Xpo4 exportin 4 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323778 Xpo4 exportin 4 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323778 Xpo4 exportin 4 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323778 Xpo4 exportin 4 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323778 Xpo4 exportin 4 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323778 Xpo4 exportin 4 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323778 Xpo4 exportin 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230119 MGI 1323778 Xpo4 exportin 4 gene MP:0012006 abnormal hippocampus physiology IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323778 Xpo4 exportin 4 gene MP:0012556 increased cell death IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323778 Xpo4 exportin 4 gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323778 Xpo4 exportin 4 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20221103 MGI PMID:36182935 1323781 Lynx1 Ly6/neurotoxin 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:16950157 1323781 Lynx1 Ly6/neurotoxin 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16950157 1323781 Lynx1 Ly6/neurotoxin 1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16950157 1323781 Lynx1 Ly6/neurotoxin 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:16950157 1323781 Lynx1 Ly6/neurotoxin 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16950157 1323781 Lynx1 Ly6/neurotoxin 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:16950157 1323781 Lynx1 Ly6/neurotoxin 1 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:16950157 1323781 Lynx1 Ly6/neurotoxin 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:16950157 1323781 Lynx1 Ly6/neurotoxin 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:16950157 1323781 Lynx1 Ly6/neurotoxin 1 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:16950157 1323781 Lynx1 Ly6/neurotoxin 1 gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:16950157 1323781 Lynx1 Ly6/neurotoxin 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:16950157 1323781 Lynx1 Ly6/neurotoxin 1 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:16950157 1323781 Lynx1 Ly6/neurotoxin 1 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:16950157 1323781 Lynx1 Ly6/neurotoxin 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16950157 1323783 Zfp503 zinc finger protein 503 gene MP:0000433 microcephaly IEA N RGD:5509061 20210520 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20231207 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200402 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20231207 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20240314 MGI PMID:32170006 1323783 Zfp503 zinc finger protein 503 gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20240314 MGI PMID:32170006 1323783 Zfp503 zinc finger protein 503 gene MP:0004103 abnormal ventral striatum morphology IAGP N RGD:5509061 20240314 MGI PMID:32170006 1323783 Zfp503 zinc finger protein 503 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20231207 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20231207 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20240314 MGI PMID:32170006 1323783 Zfp503 zinc finger protein 503 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20231207 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0009198 abnormal male genitalia morphology IEA N RGD:5509061 20230720 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0009953 abnormal olfactory tubercle morphology IAGP N RGD:5509061 20240314 MGI PMID:32170006 1323783 Zfp503 zinc finger protein 503 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1323783 Zfp503 zinc finger protein 503 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20240314 MGI PMID:32170006 1323783 Zfp503 zinc finger protein 503 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323787 Tnks1bp1 tankyrase 1 binding protein 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1323787 Tnks1bp1 tankyrase 1 binding protein 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1323789 Sox15 SRY (sex determining region Y)-box 15 gene MP:0000730 increased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:15367664 1323789 Sox15 SRY (sex determining region Y)-box 15 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15863505 1323789 Sox15 SRY (sex determining region Y)-box 15 gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20211125 MGI PMID:15367664 1323789 Sox15 SRY (sex determining region Y)-box 15 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:15367664 1323790 Uba2 ubiquitin-like modifier activating enzyme 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323794 Peak1 pseudopodium-enriched atypical kinase 1 gene MP:0000120 malocclusion IAGP N RGD:5509061 20191017 MGI PMID:29872538 1323794 Peak1 pseudopodium-enriched atypical kinase 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1323794 Peak1 pseudopodium-enriched atypical kinase 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20230601 MGI 1323794 Peak1 pseudopodium-enriched atypical kinase 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1323794 Peak1 pseudopodium-enriched atypical kinase 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 1323794 Peak1 pseudopodium-enriched atypical kinase 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220811 MGI 1323794 Peak1 pseudopodium-enriched atypical kinase 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1323794 Peak1 pseudopodium-enriched atypical kinase 1 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20230601 MGI 1323794 Peak1 pseudopodium-enriched atypical kinase 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 1323794 Peak1 pseudopodium-enriched atypical kinase 1 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20230601 MGI 1323794 Peak1 pseudopodium-enriched atypical kinase 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20230601 MGI 1323794 Peak1 pseudopodium-enriched atypical kinase 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20191017 MGI PMID:29872538 1323794 Peak1 pseudopodium-enriched atypical kinase 1 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20191017 MGI PMID:29872538 1323794 Peak1 pseudopodium-enriched atypical kinase 1 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20191017 MGI PMID:29872538 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0001147 small testis IAGP N RGD:5509061 20181220 MGI PMID:29447390 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20181220 MGI PMID:29447390 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20181220 MGI PMID:29447390 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20181220 MGI PMID:29447390 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20181220 MGI PMID:29447390 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20181220 MGI PMID:29447390 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20181220 MGI PMID:29447390 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20181220 MGI PMID:29447390 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0010039 abnormal trophoblast giant cell proliferation IAGP N RGD:5509061 20181220 MGI PMID:29447390 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20181220 MGI PMID:29447390 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20181220 MGI PMID:29447390 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20181220 MGI PMID:29447390 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20181220 MGI PMID:29447390 1323796 Pold3 polymerase (DNA-directed), delta 3, accessory subunit gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:29447390 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170525 MGI PMID:26582950 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170525 MGI PMID:26582950 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160317 MGI PMID:25222142 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0001407 short stride length IAGP N RGD:5509061 20160317 MGI PMID:25222142 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20160317 MGI PMID:25222142 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0002083 premature death IAGP N RGD:5509061 20170525 MGI PMID:26582950 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0002083 premature death IAGP N RGD:5509061 20190314 MGI PMID:30578322 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26582950 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220519 MGI 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0002690 akinesia IAGP N RGD:5509061 20160317 MGI PMID:25222142 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20160317 MGI PMID:25222142 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220519 MGI 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20170525 MGI PMID:26582950 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20160317 MGI PMID:25222142 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20190314 MGI PMID:30578322 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20160317 MGI PMID:25222142 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20160317 MGI PMID:25222142 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20160317 MGI PMID:25222142 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20170105 MGI 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170105 MGI 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20170105 MGI 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20160317 MGI PMID:25222142 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20160317 MGI PMID:25222142 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20170525 MGI PMID:26582950 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20160317 MGI PMID:25222142 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0008656 abnormal interleukin-1 beta secretion IAGP N RGD:5509061 20170525 MGI PMID:26582950 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20170525 MGI PMID:26582950 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20170525 MGI PMID:26582950 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20170525 MGI PMID:26582950 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170525 MGI PMID:26582950 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20170525 MGI PMID:26582950 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20160317 MGI PMID:25222142 1323797 Pgam5 phosphoglycerate mutase family member 5 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20170105 MGI 1323799 Plekhf2 pleckstrin homology domain containing, family F (with FYVE domain) member 2 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1323799 Plekhf2 pleckstrin homology domain containing, family F (with FYVE domain) member 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230601 MGI 1323799 Plekhf2 pleckstrin homology domain containing, family F (with FYVE domain) member 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1323799 Plekhf2 pleckstrin homology domain containing, family F (with FYVE domain) member 2 gene MP:0002989 small kidney IEA N RGD:5509061 20230601 MGI 1323799 Plekhf2 pleckstrin homology domain containing, family F (with FYVE domain) member 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230601 MGI 1323799 Plekhf2 pleckstrin homology domain containing, family F (with FYVE domain) member 2 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1323799 Plekhf2 pleckstrin homology domain containing, family F (with FYVE domain) member 2 gene MP:0011896 increased circulating unsaturated transferrin level IEA N RGD:5509061 20240523 MGI 1323801 Cnih1 cornichon family AMPA receptor auxiliary protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20562862 1323801 Cnih1 cornichon family AMPA receptor auxiliary protein 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20562862 1323801 Cnih1 cornichon family AMPA receptor auxiliary protein 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:20562862 1323809 Stk4 serine/threonine kinase 4 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:19878874 1323809 Stk4 serine/threonine kinase 4 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20080689 1323809 Stk4 serine/threonine kinase 4 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20080689 1323809 Stk4 serine/threonine kinase 4 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19692642 1323809 Stk4 serine/threonine kinase 4 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:19878874 1323809 Stk4 serine/threonine kinase 4 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:23620511 1323809 Stk4 serine/threonine kinase 4 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19878874 1323809 Stk4 serine/threonine kinase 4 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:19878874 1323809 Stk4 serine/threonine kinase 4 gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0001805 decreased IgG level IEA N RGD:5509061 20190411 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23620511 1323809 Stk4 serine/threonine kinase 4 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:23620511 1323809 Stk4 serine/threonine kinase 4 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23620511 1323809 Stk4 serine/threonine kinase 4 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19073936 1323809 Stk4 serine/threonine kinase 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:23620511 1323809 Stk4 serine/threonine kinase 4 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0002392 abnormal Peyer's patch T cell area morphology IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19692642 1323809 Stk4 serine/threonine kinase 4 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0002491 decreased IgD level IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0002494 increased IgM level IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0002497 increased IgE level IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20080689 1323809 Stk4 serine/threonine kinase 4 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19878874 1323809 Stk4 serine/threonine kinase 4 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19878874 1323809 Stk4 serine/threonine kinase 4 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20080689 1323809 Stk4 serine/threonine kinase 4 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20170223 MGI PMID:26131558 1323809 Stk4 serine/threonine kinase 4 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20080689 1323809 Stk4 serine/threonine kinase 4 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19878874 1323809 Stk4 serine/threonine kinase 4 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20080689 1323809 Stk4 serine/threonine kinase 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19878874 1323809 Stk4 serine/threonine kinase 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:19878874 1323809 Stk4 serine/threonine kinase 4 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0004265 abnormal placental transport IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19692642 1323809 Stk4 serine/threonine kinase 4 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0004978 decreased B-1 B cell number IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19692642 1323809 Stk4 serine/threonine kinase 4 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19692642 1323809 Stk4 serine/threonine kinase 4 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19692642 1323809 Stk4 serine/threonine kinase 4 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19878874 1323809 Stk4 serine/threonine kinase 4 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:19878874 1323809 Stk4 serine/threonine kinase 4 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19073936 1323809 Stk4 serine/threonine kinase 4 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0005425 increased macrophage cell number IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19692642 1323809 Stk4 serine/threonine kinase 4 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19073936 1323809 Stk4 serine/threonine kinase 4 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20080689 1323809 Stk4 serine/threonine kinase 4 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0008048 abnormal memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19073936 1323809 Stk4 serine/threonine kinase 4 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19073936 1323809 Stk4 serine/threonine kinase 4 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19692642 1323809 Stk4 serine/threonine kinase 4 gene MP:0008076 abnormal CD4-positive T cell differentiation IEA N RGD:5509061 20190411 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19073936 1323809 Stk4 serine/threonine kinase 4 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19692642 1323809 Stk4 serine/threonine kinase 4 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19692642 1323809 Stk4 serine/threonine kinase 4 gene MP:0008083 decreased single-positive T cell number IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0008122 decreased myeloid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0008126 increased dendritic cell number IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0008180 abnormal marginal zone B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:19073936 1323809 Stk4 serine/threonine kinase 4 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19073936 1323809 Stk4 serine/threonine kinase 4 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19073936 1323809 Stk4 serine/threonine kinase 4 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19073936 1323809 Stk4 serine/threonine kinase 4 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0008891 decreased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:19878874 1323809 Stk4 serine/threonine kinase 4 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20141003 MGI PMID:20080689 1323809 Stk4 serine/threonine kinase 4 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19878874 1323809 Stk4 serine/threonine kinase 4 gene MP:0009658 increased placenta apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:23620511 1323809 Stk4 serine/threonine kinase 4 gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0011018 pulmonary hyaline membrane formation IAGP N RGD:5509061 20141003 MGI PMID:23620511 1323809 Stk4 serine/threonine kinase 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19878874 1323809 Stk4 serine/threonine kinase 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0011139 increased lung endothelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23620511 1323809 Stk4 serine/threonine kinase 4 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:20080598 1323809 Stk4 serine/threonine kinase 4 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:19786569 1323809 Stk4 serine/threonine kinase 4 gene MP:0013649 decreased CD11b-high dendritic cell number IEA N RGD:5509061 20190411 MGI 1323809 Stk4 serine/threonine kinase 4 gene MP:0014348 decreased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:19339990 1323809 Stk4 serine/threonine kinase 4 gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20190411 MGI 1323813 Agmo alkylglycerol monooxygenase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20220407 MGI PMID:33726865 1323813 Agmo alkylglycerol monooxygenase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20220407 MGI PMID:33726865 1323813 Agmo alkylglycerol monooxygenase gene MP:0012220 abnormal ether lipid level IAGP N RGD:5509061 20240808 MGI PMID:36690320 1323816 Senp3 SUMO/sentrin specific peptidase 3 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20160804 MGI 1323816 Senp3 SUMO/sentrin specific peptidase 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1323820 Lnpk lunapark, ER junction formation factor gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:8978061 1323820 Lnpk lunapark, ER junction formation factor gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:2338491 1323820 Lnpk lunapark, ER junction formation factor gene MP:0001399 hyperactivity IEA N RGD:5509061 20230119 MGI 1323820 Lnpk lunapark, ER junction formation factor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:2338491 1323820 Lnpk lunapark, ER junction formation factor gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8978061 1323820 Lnpk lunapark, ER junction formation factor gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:8978061 1323820 Lnpk lunapark, ER junction formation factor gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:2338491 1323820 Lnpk lunapark, ER junction formation factor gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230119 MGI 1323820 Lnpk lunapark, ER junction formation factor gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:8978061 1323820 Lnpk lunapark, ER junction formation factor gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:2338491 1323820 Lnpk lunapark, ER junction formation factor gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:8978061 1323820 Lnpk lunapark, ER junction formation factor gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:2338491 1323820 Lnpk lunapark, ER junction formation factor gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:2338491 1323820 Lnpk lunapark, ER junction formation factor gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:8978061 1323820 Lnpk lunapark, ER junction formation factor gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:2338491 1323820 Lnpk lunapark, ER junction formation factor gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:8978061 1323820 Lnpk lunapark, ER junction formation factor gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:2338491 1323820 Lnpk lunapark, ER junction formation factor gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:8978061 1323820 Lnpk lunapark, ER junction formation factor gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:8835524 1323820 Lnpk lunapark, ER junction formation factor gene MP:0030886 decreased radius size IAGP N RGD:5509061 20181101 MGI PMID:2338491 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:21723506 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:21723506 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20160218 MGI 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0002833 increased heart weight IEA N RGD:5509061 20231207 MGI 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20141003 MGI PMID:21723506 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0008725 increased heart atrium size IEA N RGD:5509061 20170105 MGI 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21723506 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:21723506 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:21723506 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21723506 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:21723506 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21723506 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1323822 Cox15 cytochrome c oxidase assembly protein 15 gene MP:0014342 abnormal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:21723506 1323825 Tex10 testis expressed gene 10 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160526 MGI PMID:25936917 1323825 Tex10 testis expressed gene 10 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20160526 MGI PMID:25936917 1323827 Mc1r melanocortin 1 receptor gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:5713933 1323827 Mc1r melanocortin 1 receptor gene MP:0001188 hyperpigmentation IEA N RGD:5509061 20111116 MGI 1323827 Mc1r melanocortin 1 receptor gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:16988713 1323827 Mc1r melanocortin 1 receptor gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:16988713 1323827 Mc1r melanocortin 1 receptor gene MP:0001224 abnormal keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16988713 1323827 Mc1r melanocortin 1 receptor gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16988713 1323827 Mc1r melanocortin 1 receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141218 MGI PMID:18821597 1323827 Mc1r melanocortin 1 receptor gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:15994880 1323827 Mc1r melanocortin 1 receptor gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:15277941 1323827 Mc1r melanocortin 1 receptor gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:15994880 1323827 Mc1r melanocortin 1 receptor gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16988713 1323827 Mc1r melanocortin 1 receptor gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15653560 1323827 Mc1r melanocortin 1 receptor gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15653560 1323827 Mc1r melanocortin 1 receptor gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16988713 1323827 Mc1r melanocortin 1 receptor gene MP:0002671 belted IAGP N RGD:5509061 20141003 MGI PMID:5713933 1323827 Mc1r melanocortin 1 receptor gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:5713933 1323827 Mc1r melanocortin 1 receptor gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:10374067 1323827 Mc1r melanocortin 1 receptor gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:15653560 1323827 Mc1r melanocortin 1 receptor gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:17652101 1323827 Mc1r melanocortin 1 receptor gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:5713933 1323827 Mc1r melanocortin 1 receptor gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:767180 1323827 Mc1r melanocortin 1 receptor gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141218 MGI PMID:18821597 1323827 Mc1r melanocortin 1 receptor gene MP:0003136 yellow coat color IAGP N RGD:5509061 20160929 MGI PMID:27534441 1323827 Mc1r melanocortin 1 receptor gene MP:0003136 yellow coat color IAGP N RGD:5509061 20171228 MGI PMID:18715234 1323827 Mc1r melanocortin 1 receptor gene MP:0003136 yellow coat color IAGP N RGD:5509061 20190110 MGI PMID:27134165 1323827 Mc1r melanocortin 1 receptor gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16988713 1323827 Mc1r melanocortin 1 receptor gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:16988713 1323827 Mc1r melanocortin 1 receptor gene MP:0004270 analgesia IAGP N RGD:5509061 20141003 MGI PMID:15994880 1323827 Mc1r melanocortin 1 receptor gene MP:0004382 abnormal hair follicle melanogenesis IAGP N RGD:5509061 20141003 MGI PMID:1098946 1323827 Mc1r melanocortin 1 receptor gene MP:0005077 abnormal melanogenesis IAGP N RGD:5509061 20141003 MGI PMID:16988713 1323827 Mc1r melanocortin 1 receptor gene MP:0005409 darkened coat color IEA N RGD:5509061 20111116 MGI 1323827 Mc1r melanocortin 1 receptor gene MP:0006370 abnormal hair follicle pheomelanosome pheomelanin content IAGP N RGD:5509061 20141003 MGI PMID:17652101 1323827 Mc1r melanocortin 1 receptor gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20190110 MGI PMID:27134165 1323827 Mc1r melanocortin 1 receptor gene MP:0009928 abnormal pinna hair pigmentation IEA N RGD:5509061 20141003 MGI 1323827 Mc1r melanocortin 1 receptor gene MP:0009933 abnormal tail hair pigmentation IEA N RGD:5509061 20160428 MGI 1323827 Mc1r melanocortin 1 receptor gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15653560 1323827 Mc1r melanocortin 1 receptor gene MP:0011279 decreased ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15653560 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000576 clubfoot IAGP N RGD:5509061 20141003 MGI PMID:23968836 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:23968836 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18031680 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:18031680 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:21098484 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18031680 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:18031680 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18031680 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:19391113 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:19391113 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20180208 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:18031680 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21098484 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:23968836 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0004082 abnormal habenula morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0004103 abnormal ventral striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:23968836 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0004165 abnormal lateral geniculate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0008129 absent brain internal capsule IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0008129 absent brain internal capsule IAGP N RGD:5509061 20141003 MGI PMID:23968836 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:23968836 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:23968836 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:23968836 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:19391113 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19391113 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:21098484 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19391113 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17901218 1323831 Mycbp2 MYC binding protein 2, E3 ubiquitin protein ligase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1323833 Akt1s1 AKT1 substrate 1 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20160526 MGI PMID:24583056 1323833 Akt1s1 AKT1 substrate 1 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20160526 MGI PMID:24583056 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0000111 cleft palate IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0000562 polydactyly IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0000644 dextrocardia IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0000914 exencephaly IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0001293 anophthalmia IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:21725307 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0001297 microphthalmia IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:21725307 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0002766 situs inversus IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0003675 kidney cyst IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0004017 duplex kidney IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:21725307 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0005202 lethargy IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:21725307 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0006123 tricuspid valve atresia IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0006130 pulmonary valve atresia IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0008528 polycystic kidney IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0010202 focal dorsal hair loss IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0010406 common atrium IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0010413 complete atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0010865 prenatal growth retardation IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0011053 decreased respiratory motile cilia number IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0011060 abnormal kinocilium morphology IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0011254 superior-inferior ventricles IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0011510 biventricular, discordant atrioventricular connection IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0013197 decreased embryonic cilium number IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0013205 abnormal nonmotile primary cilium morphology IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331854 Cc2d2a coiled-coil and C2 domain containing 2A gene MP:0013214 decreased embryonic neuroepithelium primary cilium number IAGP N RGD:5509061 20160623 MGI PMID:24947469 1331856 Pdilt protein disulfide isomerase-like, testis expressed gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22357757 1331856 Pdilt protein disulfide isomerase-like, testis expressed gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:22357757 1331856 Pdilt protein disulfide isomerase-like, testis expressed gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220303 MGI PMID:22357757 1331857 Nepro nucleolus and neural progenitor protein gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190808 MGI 1331857 Nepro nucleolus and neural progenitor protein gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20150910 MGI PMID:26178919 1331857 Nepro nucleolus and neural progenitor protein gene MP:0008830 abnormal nucleolus morphology IAGP N RGD:5509061 20150910 MGI PMID:26178919 1331857 Nepro nucleolus and neural progenitor protein gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20150910 MGI PMID:26178919 1331857 Nepro nucleolus and neural progenitor protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1331857 Nepro nucleolus and neural progenitor protein gene MP:0012129 failure of blastocyst formation IAGP N RGD:5509061 20150910 MGI PMID:26178919 1331857 Nepro nucleolus and neural progenitor protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1331858 Gphn gephyrin gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15689563 1331858 Gphn gephyrin gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9812897 1331858 Gphn gephyrin gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:15689563 1331858 Gphn gephyrin gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:15689563 1331858 Gphn gephyrin gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:15689563 1331858 Gphn gephyrin gene MP:0001400 hyperresponsive IAGP N RGD:5509061 20141003 MGI PMID:9812897 1331858 Gphn gephyrin gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9812897 1331858 Gphn gephyrin gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:9812897 1331858 Gphn gephyrin gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:9812897 1331858 Gphn gephyrin gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:9812897 1331858 Gphn gephyrin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21209184 1331858 Gphn gephyrin gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15689563 1331858 Gphn gephyrin gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:15689563 1331858 Gphn gephyrin gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11056469 1331858 Gphn gephyrin gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:15689563 1331858 Gphn gephyrin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9812897 1331860 Tmem127 transmembrane protein 127 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20160804 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20201231 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24334765 1331860 Tmem127 transmembrane protein 127 gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20200402 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0000745 tremors IEA N RGD:5509061 20200402 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:24334765 1331860 Tmem127 transmembrane protein 127 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0005015 increased T cell number IEA N RGD:5509061 20141030 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20201231 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20210128 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20201231 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181227 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20141030 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0008124 decreased plasmacytoid dendritic cell number IEA N RGD:5509061 20201231 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20201231 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20210128 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0010851 decreased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20141030 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0012767 increased KLRG1-positive NK cell number IEA N RGD:5509061 20201022 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0012768 decreased KLRG1-positive NK cell number IEA N RGD:5509061 20201231 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0013023 decreased Ly6C high monocyte number IEA N RGD:5509061 20160804 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0013025 increased Ly6C low monocyte number IEA N RGD:5509061 20160804 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0013426 decreased memory-marker NK cell number IEA N RGD:5509061 20201231 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0013427 increased memory-marker NK cell number IEA N RGD:5509061 20201231 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0013436 increased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1331860 Tmem127 transmembrane protein 127 gene MP:0013774 decreased KLRG1-positive T-helper cell number IEA N RGD:5509061 20201231 MGI 1331863 Astn1 astrotactin 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:11861479 1331863 Astn1 astrotactin 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:11861479 1331863 Astn1 astrotactin 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11861479 1331863 Astn1 astrotactin 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:11861479 1331863 Astn1 astrotactin 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11861479 1331863 Astn1 astrotactin 1 gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:11861479 1331863 Astn1 astrotactin 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11861479 1331863 Astn1 astrotactin 1 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11861479 1331863 Astn1 astrotactin 1 gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:11861479 1331863 Astn1 astrotactin 1 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20141003 MGI PMID:11861479 1331865 Cd200r1 CD200 receptor 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20200310 MGI PMID:18424714 1331865 Cd200r1 CD200 receptor 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20220922 MGI PMID:34921782 1331865 Cd200r1 CD200 receptor 1 gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20200310 MGI PMID:17667818 1331865 Cd200r1 CD200 receptor 1 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20220922 MGI PMID:34921782 1331865 Cd200r1 CD200 receptor 1 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20200310 MGI PMID:17667818 1331865 Cd200r1 CD200 receptor 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20200310 MGI PMID:17667818 1331865 Cd200r1 CD200 receptor 1 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20200310 MGI PMID:23082204 1331865 Cd200r1 CD200 receptor 1 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:23082204 1331865 Cd200r1 CD200 receptor 1 gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20200310 MGI PMID:17667818 1331865 Cd200r1 CD200 receptor 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20200310 MGI PMID:23082204 1331865 Cd200r1 CD200 receptor 1 gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:23082204 1331865 Cd200r1 CD200 receptor 1 gene MP:0020954 decreased mechanical nociceptive threshold IAGP N RGD:5509061 20220922 MGI PMID:34921782 1331865 Cd200r1 CD200 receptor 1 gene MP:0031025 decreased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:23082204 1331866 Syne4 spectrin repeat containing, nuclear envelope family member 4 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23348741 1331866 Syne4 spectrin repeat containing, nuclear envelope family member 4 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:23348741 1331866 Syne4 spectrin repeat containing, nuclear envelope family member 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23348741 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0000416 sparse hair IEA N RGD:5509061 20141003 MGI 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:16118274 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:16118274 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:16118274 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16118274 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:16118274 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0001923 reduced female fertility IEA N RGD:5509061 20141003 MGI 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16118274 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:16118274 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:16118274 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0003849 greasy coat IEA N RGD:5509061 20141003 MGI 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0005251 blepharitis IEA N RGD:5509061 20141003 MGI 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16118274 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:16118274 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16118274 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:16118274 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0009794 sebaceous gland hyperplasia IEA N RGD:5509061 20141003 MGI 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16118274 1331867 Scd2 stearoyl-Coenzyme A desaturase 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16118274 1331868 Mylk3 myosin light chain kinase 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23095280 1331868 Mylk3 myosin light chain kinase 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:23095280 1331868 Mylk3 myosin light chain kinase 3 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20943660 1331868 Mylk3 myosin light chain kinase 3 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20943660 1331868 Mylk3 myosin light chain kinase 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:20943660 1331868 Mylk3 myosin light chain kinase 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:23095280 1331868 Mylk3 myosin light chain kinase 3 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:20943660 1331868 Mylk3 myosin light chain kinase 3 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20943660 1331868 Mylk3 myosin light chain kinase 3 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23095280 1331868 Mylk3 myosin light chain kinase 3 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:23095280 1331868 Mylk3 myosin light chain kinase 3 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:23095280 1331868 Mylk3 myosin light chain kinase 3 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:20943660 1331868 Mylk3 myosin light chain kinase 3 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:23095280 1331868 Mylk3 myosin light chain kinase 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20943660 1331868 Mylk3 myosin light chain kinase 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:23095280 1331868 Mylk3 myosin light chain kinase 3 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20943660 1331868 Mylk3 myosin light chain kinase 3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:23095280 1331868 Mylk3 myosin light chain kinase 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23095280 1331868 Mylk3 myosin light chain kinase 3 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:23095280 1331868 Mylk3 myosin light chain kinase 3 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:23095280 1331868 Mylk3 myosin light chain kinase 3 gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:20943660 1331868 Mylk3 myosin light chain kinase 3 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:20943660 1331868 Mylk3 myosin light chain kinase 3 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:23095280 1331868 Mylk3 myosin light chain kinase 3 gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:23095280 1331868 Mylk3 myosin light chain kinase 3 gene MP:0012735 abnormal response to exercise IAGP N RGD:5509061 20141003 MGI PMID:23095280 1331869 Rhebl1 Ras homolog enriched in brain like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21238928 1331869 Rhebl1 Ras homolog enriched in brain like 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21238928 1331871 Klhdc7a kelch domain containing 7A gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210422 MGI 1331873 Spon1 spondin 1, (f-spondin) extracellular matrix protein gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20150903 MGI PMID:24875054 1331873 Spon1 spondin 1, (f-spondin) extracellular matrix protein gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20150903 MGI PMID:24875054 1331873 Spon1 spondin 1, (f-spondin) extracellular matrix protein gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20150903 MGI PMID:24875054 1331873 Spon1 spondin 1, (f-spondin) extracellular matrix protein gene MP:0008838 decreased transforming growth factor beta level IAGP N RGD:5509061 20150903 MGI PMID:24875054 1331873 Spon1 spondin 1, (f-spondin) extracellular matrix protein gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20150903 MGI PMID:24875054 1331873 Spon1 spondin 1, (f-spondin) extracellular matrix protein gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20150903 MGI PMID:24875054 1331873 Spon1 spondin 1, (f-spondin) extracellular matrix protein gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20150903 MGI PMID:24875054 1331873 Spon1 spondin 1, (f-spondin) extracellular matrix protein gene MP:0013623 increased femur compact bone thickness IAGP N RGD:5509061 20150903 MGI PMID:24875054 1331873 Spon1 spondin 1, (f-spondin) extracellular matrix protein gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20150903 MGI PMID:24875054 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20160218 MGI PMID:26490870 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20160218 MGI PMID:26490870 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17349584 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20160218 MGI PMID:26490870 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17349584 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17349584 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17349584 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17349584 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20160218 MGI PMID:26490870 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20160218 MGI PMID:26490870 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:17349584 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17349584 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20160218 MGI PMID:26490870 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20160218 MGI PMID:26490870 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0008010 increased gastric adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17349584 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20160218 MGI PMID:26490870 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20160218 MGI PMID:26490870 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17349584 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17349584 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0011273 prolonged excitatory postsynaptic current decay time IAGP N RGD:5509061 20160218 MGI PMID:26490870 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:17349584 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17349584 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17349584 1331874 Lzts1 leucine zipper, putative tumor suppressor 1 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20230608 MGI PMID:17349584 1331876 Ccdc47 coiled-coil domain containing 47 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17204322 1331876 Ccdc47 coiled-coil domain containing 47 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17204322 1331876 Ccdc47 coiled-coil domain containing 47 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17204322 1331876 Ccdc47 coiled-coil domain containing 47 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17204322 1331877 Crebrf CREB3 regulatory factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160811 MGI PMID:23071095 1331877 Crebrf CREB3 regulatory factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20160811 MGI PMID:23071095 1331877 Crebrf CREB3 regulatory factor gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160811 MGI PMID:23071095 1331877 Crebrf CREB3 regulatory factor gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20160811 MGI PMID:23071095 1331877 Crebrf CREB3 regulatory factor gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20160811 MGI PMID:23071095 1331877 Crebrf CREB3 regulatory factor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160811 MGI PMID:23071095 1331877 Crebrf CREB3 regulatory factor gene MP:0001513 limb grasping IAGP N RGD:5509061 20160811 MGI PMID:23071095 1331877 Crebrf CREB3 regulatory factor gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20160811 MGI PMID:23071095 1331877 Crebrf CREB3 regulatory factor gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20160811 MGI PMID:23071095 1331877 Crebrf CREB3 regulatory factor gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20160811 MGI PMID:23071095 1331877 Crebrf CREB3 regulatory factor gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20160811 MGI PMID:23071095 1331881 Iws1 IWS1, SUPT6 interacting protein gene MP:0001399 hyperactivity IEA N RGD:5509061 20240627 MGI 1331881 Iws1 IWS1, SUPT6 interacting protein gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1331881 Iws1 IWS1, SUPT6 interacting protein gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20181025 MGI PMID:30208029 1331881 Iws1 IWS1, SUPT6 interacting protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1331881 Iws1 IWS1, SUPT6 interacting protein gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1331883 Nup210 nucleoporin 210 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20211223 MGI PMID:29736031 1331883 Nup210 nucleoporin 210 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1331883 Nup210 nucleoporin 210 gene MP:0000601 small liver IEA N RGD:5509061 20230119 MGI 1331883 Nup210 nucleoporin 210 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1331883 Nup210 nucleoporin 210 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20211223 MGI PMID:29736031 1331883 Nup210 nucleoporin 210 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20211223 MGI PMID:29736031 1331883 Nup210 nucleoporin 210 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1331883 Nup210 nucleoporin 210 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20190103 MGI PMID:30323813 1331883 Nup210 nucleoporin 210 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20211223 MGI PMID:29736031 1331883 Nup210 nucleoporin 210 gene MP:0008073 abnormal CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20211223 MGI PMID:29736031 1331883 Nup210 nucleoporin 210 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190103 MGI PMID:30323813 1331883 Nup210 nucleoporin 210 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20211223 MGI PMID:29736031 1331883 Nup210 nucleoporin 210 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20190103 MGI PMID:30323813 1331883 Nup210 nucleoporin 210 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20190103 MGI PMID:30323813 1331883 Nup210 nucleoporin 210 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20190103 MGI PMID:30323813 1331883 Nup210 nucleoporin 210 gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20190103 MGI PMID:30323813 1331883 Nup210 nucleoporin 210 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IAGP N RGD:5509061 20190103 MGI PMID:30323813 1331883 Nup210 nucleoporin 210 gene MP:0012762 abnormal alpha-beta T cell morphology IAGP N RGD:5509061 20190103 MGI PMID:30323813 1331883 Nup210 nucleoporin 210 gene MP:0012765 decreased alpha-beta T cell number IAGP N RGD:5509061 20190103 MGI PMID:30323813 1331883 Nup210 nucleoporin 210 gene MP:0013772 increased effector memory T-helper cell number IAGP N RGD:5509061 20211223 MGI PMID:29736031 1331884 Dlgap3 DLG associated protein 3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:17713528 1331884 Dlgap3 DLG associated protein 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17713528 1331884 Dlgap3 DLG associated protein 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:17713528 1331884 Dlgap3 DLG associated protein 3 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:17713528 1331884 Dlgap3 DLG associated protein 3 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:17713528 1331884 Dlgap3 DLG associated protein 3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:17713528 1331884 Dlgap3 DLG associated protein 3 gene MP:0003234 enhanced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17713528 1331884 Dlgap3 DLG associated protein 3 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:17713528 1331884 Dlgap3 DLG associated protein 3 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17713528 1331885 Rmnd5b required for meiotic nuclear division 5 homolog B gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 1331887 Sdhaf2 succinate dehydrogenase complex assembly factor 2 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191205 MGI 1331887 Sdhaf2 succinate dehydrogenase complex assembly factor 2 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1331887 Sdhaf2 succinate dehydrogenase complex assembly factor 2 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191205 MGI 1331887 Sdhaf2 succinate dehydrogenase complex assembly factor 2 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1331887 Sdhaf2 succinate dehydrogenase complex assembly factor 2 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191205 MGI 1331887 Sdhaf2 succinate dehydrogenase complex assembly factor 2 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191205 MGI 1331887 Sdhaf2 succinate dehydrogenase complex assembly factor 2 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1331887 Sdhaf2 succinate dehydrogenase complex assembly factor 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1331887 Sdhaf2 succinate dehydrogenase complex assembly factor 2 gene MP:0012724 absent head fold IEA N RGD:5509061 20191205 MGI 1331887 Sdhaf2 succinate dehydrogenase complex assembly factor 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191205 MGI 1331890 Telo2 telomere maintenance 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18160036 1331890 Telo2 telomere maintenance 2 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:18160036 1331890 Telo2 telomere maintenance 2 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:18160036 1331890 Telo2 telomere maintenance 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1331890 Telo2 telomere maintenance 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18160036 1331890 Telo2 telomere maintenance 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1331890 Telo2 telomere maintenance 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1331894 Nln neurolysin (metallopeptidase M3 family) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:24719317 1331894 Nln neurolysin (metallopeptidase M3 family) gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141106 MGI PMID:24719317 1331894 Nln neurolysin (metallopeptidase M3 family) gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141106 MGI PMID:24719317 1331894 Nln neurolysin (metallopeptidase M3 family) gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141106 MGI PMID:24719317 1331894 Nln neurolysin (metallopeptidase M3 family) gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141106 MGI PMID:24719317 1331894 Nln neurolysin (metallopeptidase M3 family) gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141106 MGI PMID:24719317 1331895 Sh3d19 SH3 domain protein D19 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20230622 MGI PMID:25671302 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230622 MGI PMID:25671302 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20230622 MGI PMID:25671302 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20230622 MGI PMID:25671302 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20230622 MGI PMID:25671302 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20230622 MGI PMID:25671302 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20230622 MGI PMID:25671302 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20230622 MGI PMID:25671302 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20230622 MGI PMID:25671302 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20240523 MGI 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20230622 MGI PMID:25671302 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20230622 MGI PMID:25671302 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230601 MGI 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20230622 MGI PMID:25671302 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20230622 MGI PMID:25671302 1331899 Puf60 poly-U binding splicing factor 60 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1331903 Tysnd1 trypsin domain containing 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20151126 MGI PMID:23459139 1331903 Tysnd1 trypsin domain containing 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20151126 MGI PMID:23459139 1331903 Tysnd1 trypsin domain containing 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20151126 MGI PMID:23459139 1331903 Tysnd1 trypsin domain containing 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20151126 MGI PMID:23459139 1331903 Tysnd1 trypsin domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20151126 MGI PMID:23459139 1331903 Tysnd1 trypsin domain containing 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160211 MGI PMID:23459139 1331903 Tysnd1 trypsin domain containing 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20151126 MGI PMID:23459139 1331903 Tysnd1 trypsin domain containing 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20151126 MGI PMID:23459139 1331903 Tysnd1 trypsin domain containing 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20151126 MGI PMID:23459139 1331903 Tysnd1 trypsin domain containing 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20151126 MGI PMID:23459139 1331903 Tysnd1 trypsin domain containing 1 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20151126 MGI PMID:23459139 1331903 Tysnd1 trypsin domain containing 1 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20151126 MGI PMID:23459139 1331903 Tysnd1 trypsin domain containing 1 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20151126 MGI PMID:23459139 1331903 Tysnd1 trypsin domain containing 1 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20151126 MGI PMID:23459139 1331903 Tysnd1 trypsin domain containing 1 gene MP:0012216 decreased plasmalogen level IAGP N RGD:5509061 20151126 MGI PMID:23459139 1331904 Zbtb14 zinc finger and BTB domain containing 14 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1331904 Zbtb14 zinc finger and BTB domain containing 14 gene MP:0000285 abnormal heart valve morphology IEA N RGD:5509061 20141003 MGI 1331904 Zbtb14 zinc finger and BTB domain containing 14 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20141003 MGI 1331904 Zbtb14 zinc finger and BTB domain containing 14 gene MP:0000914 exencephaly IEA N RGD:5509061 20141003 MGI 1331904 Zbtb14 zinc finger and BTB domain containing 14 gene MP:0003675 kidney cyst IEA N RGD:5509061 20141003 MGI 1331904 Zbtb14 zinc finger and BTB domain containing 14 gene MP:0004017 duplex kidney IEA N RGD:5509061 20141003 MGI 1331904 Zbtb14 zinc finger and BTB domain containing 14 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1331904 Zbtb14 zinc finger and BTB domain containing 14 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20141003 MGI 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0000692 small spleen IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0001577 anemia IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20201022 MGI 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20201022 MGI 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0002083 premature death IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20201022 MGI 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20201022 MGI 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0003701 elevated level of mitotic sister chromatid exchange IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0003707 increased cell nucleus count IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20201022 MGI 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0003786 premature aging IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0003902 abnormal cell mass IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0006204 embryonic lethality before implantation IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0009567 mitotic nondisjunction IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0010291 increased cardiovascular system tumor incidence IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20170824 MGI PMID:26443207 1331905 Nsmce2 NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1331906 Rpain RPA interacting protein gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1331906 Rpain RPA interacting protein gene MP:0005028 abnormal trophectoderm morphology IEA N RGD:5509061 20240801 MGI 1331906 Rpain RPA interacting protein gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 1331906 Rpain RPA interacting protein gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1331906 Rpain RPA interacting protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1331906 Rpain RPA interacting protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1331906 Rpain RPA interacting protein gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240801 MGI 1331908 Arsg arylsulfatase G gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0003354 astrocytosis IAGP N RGD:5509061 20191219 MGI PMID:26975023 1331908 Arsg arylsulfatase G gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0004967 abnormal kidney epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0008242 abnormal perivascular macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20191219 MGI PMID:26975023 1331908 Arsg arylsulfatase G gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20191219 MGI PMID:26975023 1331908 Arsg arylsulfatase G gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20191219 MGI PMID:26975023 1331908 Arsg arylsulfatase G gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0008918 microgliosis IAGP N RGD:5509061 20191219 MGI PMID:26975023 1331908 Arsg arylsulfatase G gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0010369 abnormal thalamus neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0011475 abnormal glycosaminoglycan level IAGP N RGD:5509061 20141003 MGI PMID:22689975 1331908 Arsg arylsulfatase G gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20191219 MGI PMID:26975023 1331908 Arsg arylsulfatase G gene MP:0031148 abnormal liver sinusoidal endothelial cell morphology IAGP N RGD:5509061 20201015 MGI PMID:22689975 1331911 Clip3 CAP-GLY domain containing linker protein 3 gene MP:0000738 impaired muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:23482493 1331911 Clip3 CAP-GLY domain containing linker protein 3 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:23482493 1331911 Clip3 CAP-GLY domain containing linker protein 3 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:23482493 1331911 Clip3 CAP-GLY domain containing linker protein 3 gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:23482493 1331911 Clip3 CAP-GLY domain containing linker protein 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:23482493 1331911 Clip3 CAP-GLY domain containing linker protein 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:23482493 1331911 Clip3 CAP-GLY domain containing linker protein 3 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:23482493 1331911 Clip3 CAP-GLY domain containing linker protein 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23482493 1331911 Clip3 CAP-GLY domain containing linker protein 3 gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20141003 MGI PMID:23482493 1331913 Trak2 trafficking protein, kinesin binding 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1331913 Trak2 trafficking protein, kinesin binding 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1331913 Trak2 trafficking protein, kinesin binding 2 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 1331913 Trak2 trafficking protein, kinesin binding 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1331913 Trak2 trafficking protein, kinesin binding 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1331913 Trak2 trafficking protein, kinesin binding 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1331913 Trak2 trafficking protein, kinesin binding 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1331913 Trak2 trafficking protein, kinesin binding 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1331914 Dab2ip disabled 2 interacting protein gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:23326475 1331914 Dab2ip disabled 2 interacting protein gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18281285 1331914 Dab2ip disabled 2 interacting protein gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:18281285 1331916 Mustn1 musculoskeletal, embryonic nuclear protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240404 MGI PMID:38458566 1331916 Mustn1 musculoskeletal, embryonic nuclear protein 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20240404 MGI PMID:38458566 1331916 Mustn1 musculoskeletal, embryonic nuclear protein 1 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20240404 MGI PMID:38458566 1331917 Mfsd8 major facilitator superfamily domain containing 8 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141127 MGI PMID:24423645 1331917 Mfsd8 major facilitator superfamily domain containing 8 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141127 MGI PMID:24423645 1331917 Mfsd8 major facilitator superfamily domain containing 8 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141127 MGI PMID:24423645 1331917 Mfsd8 major facilitator superfamily domain containing 8 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1331917 Mfsd8 major facilitator superfamily domain containing 8 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160421 MGI 1331917 Mfsd8 major facilitator superfamily domain containing 8 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141127 MGI PMID:24423645 1331917 Mfsd8 major facilitator superfamily domain containing 8 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20160421 MGI 1331917 Mfsd8 major facilitator superfamily domain containing 8 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141127 MGI PMID:24423645 1331917 Mfsd8 major facilitator superfamily domain containing 8 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141127 MGI PMID:24423645 1331917 Mfsd8 major facilitator superfamily domain containing 8 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141127 MGI PMID:24423645 1331917 Mfsd8 major facilitator superfamily domain containing 8 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1331917 Mfsd8 major facilitator superfamily domain containing 8 gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141127 MGI PMID:24423645 1331917 Mfsd8 major facilitator superfamily domain containing 8 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20160421 MGI 1331917 Mfsd8 major facilitator superfamily domain containing 8 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141127 MGI PMID:24423645 1331917 Mfsd8 major facilitator superfamily domain containing 8 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141127 MGI PMID:24423645 1331918 Ptpru protein tyrosine phosphatase receptor type U gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220519 MGI 1331918 Ptpru protein tyrosine phosphatase receptor type U gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1331918 Ptpru protein tyrosine phosphatase receptor type U gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1331918 Ptpru protein tyrosine phosphatase receptor type U gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20170105 MGI 1331920 Tomm40 translocase of outer mitochondrial membrane 40 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 1331920 Tomm40 translocase of outer mitochondrial membrane 40 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1331920 Tomm40 translocase of outer mitochondrial membrane 40 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1331920 Tomm40 translocase of outer mitochondrial membrane 40 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1331920 Tomm40 translocase of outer mitochondrial membrane 40 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1331920 Tomm40 translocase of outer mitochondrial membrane 40 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1331920 Tomm40 translocase of outer mitochondrial membrane 40 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1331920 Tomm40 translocase of outer mitochondrial membrane 40 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1331921 Large2 LARGE xylosyl- and glucuronyltransferase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160929 MGI PMID:25138275 1331921 Large2 LARGE xylosyl- and glucuronyltransferase 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 1331921 Large2 LARGE xylosyl- and glucuronyltransferase 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 1331922 Nexn nexilin gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20160804 MGI PMID:26659360 1331922 Nexn nexilin gene MP:0000274 enlarged heart IAGP N RGD:5509061 20210415 MGI PMID:30982350 1331922 Nexn nexilin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20210401 MGI PMID:32814711 1331922 Nexn nexilin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20210415 MGI PMID:30982350 1331922 Nexn nexilin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210415 MGI PMID:30982350 1331922 Nexn nexilin gene MP:0001265 decreased body size IAGP N RGD:5509061 20210415 MGI PMID:30982350 1331922 Nexn nexilin gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20160804 MGI PMID:26659360 1331922 Nexn nexilin gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20210415 MGI PMID:30982350 1331922 Nexn nexilin gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20160804 MGI PMID:26659360 1331922 Nexn nexilin gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20210401 MGI PMID:32814711 1331922 Nexn nexilin gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20210415 MGI PMID:30982350 1331922 Nexn nexilin gene MP:0002833 increased heart weight IAGP N RGD:5509061 20160804 MGI PMID:26659360 1331922 Nexn nexilin gene MP:0002833 increased heart weight IAGP N RGD:5509061 20210415 MGI PMID:30982350 1331922 Nexn nexilin gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20160804 MGI PMID:26659360 1331922 Nexn nexilin gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20210415 MGI PMID:30982350 1331922 Nexn nexilin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160804 MGI PMID:26659360 1331922 Nexn nexilin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20210401 MGI PMID:32814711 1331922 Nexn nexilin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20210415 MGI PMID:30982350 1331922 Nexn nexilin gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20160804 MGI PMID:26659360 1331922 Nexn nexilin gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20210401 MGI PMID:32814711 1331922 Nexn nexilin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210415 MGI PMID:30982350 1331922 Nexn nexilin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160804 MGI PMID:26659360 1331922 Nexn nexilin gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210401 MGI PMID:32814711 1331922 Nexn nexilin gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20210401 MGI PMID:32814711 1331922 Nexn nexilin gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20210415 MGI PMID:30982350 1331922 Nexn nexilin gene MP:0031147 abnormal ventricular thrombosis IAGP N RGD:5509061 20210415 MGI PMID:30982350 1331923 Rnase6 ribonuclease, RNase A family, 6 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210128 MGI 1331923 Rnase6 ribonuclease, RNase A family, 6 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 1331923 Rnase6 ribonuclease, RNase A family, 6 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210128 MGI 1331923 Rnase6 ribonuclease, RNase A family, 6 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 1331924 Ints3 integrator complex subunit 3 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201022 MGI 1331924 Ints3 integrator complex subunit 3 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1331924 Ints3 integrator complex subunit 3 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1331924 Ints3 integrator complex subunit 3 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1331924 Ints3 integrator complex subunit 3 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1331924 Ints3 integrator complex subunit 3 gene MP:0005655 increased aggression IEA N RGD:5509061 20201022 MGI 1331924 Ints3 integrator complex subunit 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1331924 Ints3 integrator complex subunit 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1331924 Ints3 integrator complex subunit 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1331925 Cenpt centromere protein T gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1331925 Cenpt centromere protein T gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1331925 Cenpt centromere protein T gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20160602 MGI PMID:23459151 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20160602 MGI PMID:23459151 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210422 MGI 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20160602 MGI PMID:23459151 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20210422 MGI 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0004340 short scapula IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0004347 abnormal scapular spine morphology IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0005430 absent fibula IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20160602 MGI PMID:23459151 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20160602 MGI PMID:23459151 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20160602 MGI PMID:23459151 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20160602 MGI PMID:23459151 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160602 MGI PMID:23459151 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210422 MGI 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160602 MGI PMID:23459151 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20150312 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:22940690 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:23408915 1331927 Nabp2 nucleic acid binding protein 2 gene MP:0014473 increased pulmonary alveolus wall thickness IAGP N RGD:5509061 20240704 MGI PMID:23408915 1331928 Adgrl2 adhesion G protein-coupled receptor L2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20210128 MGI PMID:31206334 1331928 Adgrl2 adhesion G protein-coupled receptor L2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20141003 MGI 1331928 Adgrl2 adhesion G protein-coupled receptor L2 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20210128 MGI PMID:31206334 1331928 Adgrl2 adhesion G protein-coupled receptor L2 gene MP:0003922 abnormal heart right atrium morphology IAGP N RGD:5509061 20210128 MGI PMID:31206334 1331928 Adgrl2 adhesion G protein-coupled receptor L2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20210128 MGI PMID:31206334 1331928 Adgrl2 adhesion G protein-coupled receptor L2 gene MP:0010432 common ventricle IAGP N RGD:5509061 20210128 MGI PMID:31206334 1331928 Adgrl2 adhesion G protein-coupled receptor L2 gene MP:0010580 decreased heart left ventricle size IAGP N RGD:5509061 20210128 MGI PMID:31206334 1331928 Adgrl2 adhesion G protein-coupled receptor L2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210128 MGI PMID:31206334 1331928 Adgrl2 adhesion G protein-coupled receptor L2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IEA N RGD:5509061 20141003 MGI 1331929 Slc16a10 solute carrier family 16 (monocarboxylic acid transporters), member 10 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20160211 MGI PMID:26438296 1331929 Slc16a10 solute carrier family 16 (monocarboxylic acid transporters), member 10 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:23045339 1331929 Slc16a10 solute carrier family 16 (monocarboxylic acid transporters), member 10 gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:23045339 1331929 Slc16a10 solute carrier family 16 (monocarboxylic acid transporters), member 10 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:23045339 1331929 Slc16a10 solute carrier family 16 (monocarboxylic acid transporters), member 10 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:23045339 1331929 Slc16a10 solute carrier family 16 (monocarboxylic acid transporters), member 10 gene MP:0009349 increased urine pH IAGP N RGD:5509061 20141003 MGI PMID:23045339 1331929 Slc16a10 solute carrier family 16 (monocarboxylic acid transporters), member 10 gene MP:0011468 abnormal urine amino acid level IAGP N RGD:5509061 20141003 MGI PMID:23045339 1331929 Slc16a10 solute carrier family 16 (monocarboxylic acid transporters), member 10 gene MP:0011470 increased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:23045339 1331929 Slc16a10 solute carrier family 16 (monocarboxylic acid transporters), member 10 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:23045339 1331933 Gk5 glycerol kinase 5 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20180208 MGI PMID:28607088 1331933 Gk5 glycerol kinase 5 gene MP:0000414 alopecia IAGP N RGD:5509061 20180208 MGI PMID:28607088 1331933 Gk5 glycerol kinase 5 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20180208 MGI PMID:28607088 1331933 Gk5 glycerol kinase 5 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20180208 MGI PMID:28607088 1331933 Gk5 glycerol kinase 5 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20180208 MGI PMID:28607088 1331933 Gk5 glycerol kinase 5 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20180208 MGI PMID:28607088 1331933 Gk5 glycerol kinase 5 gene MP:0002992 abnormal sebaceous lipid secretion IAGP N RGD:5509061 20180208 MGI PMID:28607088 1331933 Gk5 glycerol kinase 5 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20180208 MGI PMID:28607088 1331933 Gk5 glycerol kinase 5 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20180208 MGI PMID:28607088 1331933 Gk5 glycerol kinase 5 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20180208 MGI PMID:28607088 1331933 Gk5 glycerol kinase 5 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20180208 MGI PMID:28607088 1331933 Gk5 glycerol kinase 5 gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20180208 MGI PMID:28607088 1331933 Gk5 glycerol kinase 5 gene MP:0008860 abnormal hair cycle telogen phase IAGP N RGD:5509061 20180208 MGI PMID:28607088 1331933 Gk5 glycerol kinase 5 gene MP:0009004 progressive hair loss IEA N RGD:5509061 20181004 MGI 1331933 Gk5 glycerol kinase 5 gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20180208 MGI PMID:28607088 1331933 Gk5 glycerol kinase 5 gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20181011 MGI 1331933 Gk5 glycerol kinase 5 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1331933 Gk5 glycerol kinase 5 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20180208 MGI PMID:28607088 1331933 Gk5 glycerol kinase 5 gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1331934 Prom1 prominin 1 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19228982 1331934 Prom1 prominin 1 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19228982 1331934 Prom1 prominin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19718438 1331934 Prom1 prominin 1 gene MP:0001324 abnormal eye pigmentation IEA N RGD:5509061 20141218 MGI 1331934 Prom1 prominin 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:19228982 1331934 Prom1 prominin 1 gene MP:0001326 retina degeneration IEA N RGD:5509061 20141218 MGI 1331934 Prom1 prominin 1 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20200123 MGI PMID:25414197 1331934 Prom1 prominin 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19718438 1331934 Prom1 prominin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19092805 1331934 Prom1 prominin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19092805 1331934 Prom1 prominin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19718438 1331934 Prom1 prominin 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19228982 1331934 Prom1 prominin 1 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19092805 1331934 Prom1 prominin 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19228982 1331934 Prom1 prominin 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200123 MGI PMID:25414197 1331934 Prom1 prominin 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19228982 1331934 Prom1 prominin 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200123 MGI PMID:25414197 1331934 Prom1 prominin 1 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:19228982 1331934 Prom1 prominin 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19228982 1331934 Prom1 prominin 1 gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:19228982 1331934 Prom1 prominin 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:19228982 1331934 Prom1 prominin 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200123 MGI PMID:25414197 1331934 Prom1 prominin 1 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:19228982 1331934 Prom1 prominin 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:25414197 1331934 Prom1 prominin 1 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20200123 MGI PMID:25414197 1331934 Prom1 prominin 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:25414197 1331934 Prom1 prominin 1 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:19228982 1331934 Prom1 prominin 1 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200123 MGI PMID:25414197 1331934 Prom1 prominin 1 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20200123 MGI PMID:25414197 1331934 Prom1 prominin 1 gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20200123 MGI PMID:25414197 1331934 Prom1 prominin 1 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:19228982 1331934 Prom1 prominin 1 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20200123 MGI PMID:25414197 1331934 Prom1 prominin 1 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20200123 MGI PMID:25414197 1331934 Prom1 prominin 1 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200123 MGI PMID:25414197 1331934 Prom1 prominin 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20141218 MGI 1331934 Prom1 prominin 1 gene MP:0012029 abnormal electroretinogram waveform feature IEA N RGD:5509061 20141218 MGI 1331934 Prom1 prominin 1 gene MP:0012143 decreased a-wave amplitude IEA N RGD:5509061 20141218 MGI 1331934 Prom1 prominin 1 gene MP:0012144 decreased b-wave amplitude IEA N RGD:5509061 20141218 MGI 1331934 Prom1 prominin 1 gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20160428 MGI PMID:19718438 1331934 Prom1 prominin 1 gene MP:0014333 short retina cone cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:19228982 1331934 Prom1 prominin 1 gene MP:0020816 decreased photoreceptor outer segment number IAGP N RGD:5509061 20200123 MGI PMID:25414197 1331935 Poc5 POC5 centriolar protein gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20181227 MGI 1331935 Poc5 POC5 centriolar protein gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 1331935 Poc5 POC5 centriolar protein gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20221215 MGI 1331935 Poc5 POC5 centriolar protein gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1331935 Poc5 POC5 centriolar protein gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0002244 abnormal turbinate morphology IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200310 MGI PMID:22820017 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0011229 abnormal vitamin C level IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0011229 abnormal vitamin C level IAGP N RGD:5509061 20200310 MGI PMID:22820017 1331936 Akr1a1 aldo-keto reductase family 1, member A1 gene MP:0030884 rachitic rosary IAGP N RGD:5509061 20200310 MGI PMID:20410296 1331938 Trmt1 tRNA methyltransferase 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20181227 MGI 1331938 Trmt1 tRNA methyltransferase 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1331938 Trmt1 tRNA methyltransferase 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1331938 Trmt1 tRNA methyltransferase 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20210128 MGI 1331938 Trmt1 tRNA methyltransferase 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1331938 Trmt1 tRNA methyltransferase 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20210128 MGI 1331938 Trmt1 tRNA methyltransferase 1 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20211021 MGI 1331938 Trmt1 tRNA methyltransferase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1331939 Mettl18 methyltransferase like 18 gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1331939 Mettl18 methyltransferase like 18 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20240523 MGI 1331939 Mettl18 methyltransferase like 18 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220811 MGI 1331939 Mettl18 methyltransferase like 18 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220519 MGI 1331939 Mettl18 methyltransferase like 18 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1331939 Mettl18 methyltransferase like 18 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220519 MGI 1331940 Dlgap4 DLG associated protein 4 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1331940 Dlgap4 DLG associated protein 4 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1331940 Dlgap4 DLG associated protein 4 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1331940 Dlgap4 DLG associated protein 4 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1331940 Dlgap4 DLG associated protein 4 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1331940 Dlgap4 DLG associated protein 4 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20200402 MGI 1331940 Dlgap4 DLG associated protein 4 gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0020513 abnormal dendritic stubby spine morphology IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20190919 MGI PMID:30664629 1331940 Dlgap4 DLG associated protein 4 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:30664629 1331943 Pou2f3 POU domain, class 2, transcription factor 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1331943 Pou2f3 POU domain, class 2, transcription factor 3 gene MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20141003 MGI PMID:21572433 1331943 Pou2f3 POU domain, class 2, transcription factor 3 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:9242494 1331943 Pou2f3 POU domain, class 2, transcription factor 3 gene MP:0004209 abnormal sweet taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21572433 1331943 Pou2f3 POU domain, class 2, transcription factor 3 gene MP:0004210 abnormal bitter taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21572433 1331943 Pou2f3 POU domain, class 2, transcription factor 3 gene MP:0004213 abnormal umami taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21572433 1331943 Pou2f3 POU domain, class 2, transcription factor 3 gene MP:0006260 abnormal gustatory papilla taste bud morphology IAGP N RGD:5509061 20141003 MGI PMID:21572433 1331943 Pou2f3 POU domain, class 2, transcription factor 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9242494 1331944 Fbln7 fibulin 7 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20191003 MGI PMID:29730503 1331944 Fbln7 fibulin 7 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20191003 MGI PMID:29730503 1331944 Fbln7 fibulin 7 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20191003 MGI PMID:29730503 1331944 Fbln7 fibulin 7 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20191003 MGI PMID:29730503 1331944 Fbln7 fibulin 7 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20191003 MGI PMID:29730503 1331946 Arhgdig Rho GDP dissociation inhibitor gamma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16054116 1331947 Nabp1 nucleic acid binding protein 1 gene MP:0001147 small testis IAGP N RGD:5509061 20180719 MGI PMID:25917330 1331947 Nabp1 nucleic acid binding protein 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180719 MGI PMID:25917330 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19723493 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170105 MGI 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20170105 MGI 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0002830 gallstones IAGP N RGD:5509061 20141003 MGI PMID:16724960 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:16724960 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:16724960 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0005084 abnormal gallbladder morphology IAGP N RGD:5509061 20141003 MGI PMID:16724960 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17065403 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16724960 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19723493 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17065403 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17065403 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:17065403 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19723493 1331948 Gpbar1 G protein-coupled bile acid receptor 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20220721 MGI PMID:34329568 1331949 Top1mt DNA topoisomerase 1, mitochondrial gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:22911747 1331949 Top1mt DNA topoisomerase 1, mitochondrial gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20141003 MGI PMID:22911747 1331949 Top1mt DNA topoisomerase 1, mitochondrial gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22911747 1331949 Top1mt DNA topoisomerase 1, mitochondrial gene MP:0003925 abnormal cellular glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:22911747 1331949 Top1mt DNA topoisomerase 1, mitochondrial gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22911747 1331949 Top1mt DNA topoisomerase 1, mitochondrial gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:22911747 1331949 Top1mt DNA topoisomerase 1, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:22911747 1331949 Top1mt DNA topoisomerase 1, mitochondrial gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:22911747 1331949 Top1mt DNA topoisomerase 1, mitochondrial gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22911747 1331949 Top1mt DNA topoisomerase 1, mitochondrial gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:22911747 1331949 Top1mt DNA topoisomerase 1, mitochondrial gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:22911747 1331949 Top1mt DNA topoisomerase 1, mitochondrial gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22911747 1331953 Prelid1 PRELI domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22666421 1331954 Frmd4b FERM domain containing 4B gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1331954 Frmd4b FERM domain containing 4B gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20200310 MGI 1331955 Ubash3b ubiquitin associated and SH3 domain containing, B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170323 MGI PMID:12370296 1331955 Ubash3b ubiquitin associated and SH3 domain containing, B gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20170323 MGI PMID:14738763 1331955 Ubash3b ubiquitin associated and SH3 domain containing, B gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20170323 MGI PMID:14738763 1331955 Ubash3b ubiquitin associated and SH3 domain containing, B gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20170323 MGI PMID:14738763 1331955 Ubash3b ubiquitin associated and SH3 domain containing, B gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20170323 MGI PMID:14738763 1331955 Ubash3b ubiquitin associated and SH3 domain containing, B gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20170323 MGI PMID:14738763 1331956 Crip2 cysteine rich protein 2 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20151217 MGI PMID:18256252 1331956 Crip2 cysteine rich protein 2 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20151217 MGI PMID:18256252 1331958 Prkci protein kinase C, iota gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15322187 1331958 Prkci protein kinase C, iota gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:16267237 1331958 Prkci protein kinase C, iota gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:16267237 1331958 Prkci protein kinase C, iota gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19835853 1331958 Prkci protein kinase C, iota gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:19835853 1331958 Prkci protein kinase C, iota gene MP:0001318 pupil opacity IAGP N RGD:5509061 20141003 MGI PMID:19835853 1331958 Prkci protein kinase C, iota gene MP:0001320 small pupil IAGP N RGD:5509061 20141003 MGI PMID:19835853 1331958 Prkci protein kinase C, iota gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:19835853 1331958 Prkci protein kinase C, iota gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:16267237 1331958 Prkci protein kinase C, iota gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0001705 abnormal proximal-distal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19279126 1331958 Prkci protein kinase C, iota gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:16267237 1331958 Prkci protein kinase C, iota gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19279126 1331958 Prkci protein kinase C, iota gene MP:0002579 disorganized secondary lens fibers IAGP N RGD:5509061 20141003 MGI PMID:19835853 1331958 Prkci protein kinase C, iota gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0002694 abnormal pancreas secretion IAGP N RGD:5509061 20141003 MGI PMID:15630453 1331958 Prkci protein kinase C, iota gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:19279126 1331958 Prkci protein kinase C, iota gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:19279126 1331958 Prkci protein kinase C, iota gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19835853 1331958 Prkci protein kinase C, iota gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:19279126 1331958 Prkci protein kinase C, iota gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0004559 small allantois IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:19835853 1331958 Prkci protein kinase C, iota gene MP:0005199 abnormal iris pigment epithelium IAGP N RGD:5509061 20141003 MGI PMID:19835853 1331958 Prkci protein kinase C, iota gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19279126 1331958 Prkci protein kinase C, iota gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15630453 1331958 Prkci protein kinase C, iota gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19279126 1331958 Prkci protein kinase C, iota gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15630453 1331958 Prkci protein kinase C, iota gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:19279126 1331958 Prkci protein kinase C, iota gene MP:0008062 abnormal podocyte slit junction morphology IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0008062 abnormal podocyte slit junction morphology IAGP N RGD:5509061 20141003 MGI PMID:19279126 1331958 Prkci protein kinase C, iota gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:19279126 1331958 Prkci protein kinase C, iota gene MP:0008583 absent photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:16267237 1331958 Prkci protein kinase C, iota gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:16267237 1331958 Prkci protein kinase C, iota gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15322187 1331958 Prkci protein kinase C, iota gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0011190 thick embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0011257 abnormal head fold morphology IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:19279126 1331958 Prkci protein kinase C, iota gene MP:0011483 renal glomerular synechia IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0011509 dilated glomerular capillary IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0011869 detached podocyte IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0011870 abnormal podocyte polarity IAGP N RGD:5509061 20141003 MGI PMID:19142224 1331958 Prkci protein kinase C, iota gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0012081 absent heart tube IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0012104 small amniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:23690951 1331958 Prkci protein kinase C, iota gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0030020 decreased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0030022 decreased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:17641777 1331958 Prkci protein kinase C, iota gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:17641777 1331960 Enpp3 ectonucleotide pyrophosphatase/phosphodiesterase 3 gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20160421 MGI PMID:25692702 1331960 Enpp3 ectonucleotide pyrophosphatase/phosphodiesterase 3 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20160421 MGI PMID:25692702 1331960 Enpp3 ectonucleotide pyrophosphatase/phosphodiesterase 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20160421 MGI PMID:25692702 1331960 Enpp3 ectonucleotide pyrophosphatase/phosphodiesterase 3 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20160421 MGI PMID:25692702 1331960 Enpp3 ectonucleotide pyrophosphatase/phosphodiesterase 3 gene MP:0002464 abnormal basophil physiology IAGP N RGD:5509061 20160421 MGI PMID:25692702 1331960 Enpp3 ectonucleotide pyrophosphatase/phosphodiesterase 3 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20160421 MGI PMID:25692702 1331960 Enpp3 ectonucleotide pyrophosphatase/phosphodiesterase 3 gene MP:0002606 increased basophil cell number IAGP N RGD:5509061 20160421 MGI PMID:25692702 1331960 Enpp3 ectonucleotide pyrophosphatase/phosphodiesterase 3 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20160421 MGI PMID:25692702 1331960 Enpp3 ectonucleotide pyrophosphatase/phosphodiesterase 3 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20160421 MGI PMID:25692702 1331960 Enpp3 ectonucleotide pyrophosphatase/phosphodiesterase 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20160421 MGI PMID:25692702 1331960 Enpp3 ectonucleotide pyrophosphatase/phosphodiesterase 3 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20160421 MGI PMID:25692702 1331960 Enpp3 ectonucleotide pyrophosphatase/phosphodiesterase 3 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160421 MGI PMID:25692702 1331961 Arl6ip5 ADP-ribosylation factor-like 6 interacting protein 5 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:22461904 1331961 Arl6ip5 ADP-ribosylation factor-like 6 interacting protein 5 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22461904 1331961 Arl6ip5 ADP-ribosylation factor-like 6 interacting protein 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22210510 1331961 Arl6ip5 ADP-ribosylation factor-like 6 interacting protein 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22461904 1331961 Arl6ip5 ADP-ribosylation factor-like 6 interacting protein 5 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22210510 1331961 Arl6ip5 ADP-ribosylation factor-like 6 interacting protein 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22461904 1331961 Arl6ip5 ADP-ribosylation factor-like 6 interacting protein 5 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:22461904 1331961 Arl6ip5 ADP-ribosylation factor-like 6 interacting protein 5 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:22210510 1331961 Arl6ip5 ADP-ribosylation factor-like 6 interacting protein 5 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20141003 MGI PMID:22210510 1331961 Arl6ip5 ADP-ribosylation factor-like 6 interacting protein 5 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22461904 1331961 Arl6ip5 ADP-ribosylation factor-like 6 interacting protein 5 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22461904 1331961 Arl6ip5 ADP-ribosylation factor-like 6 interacting protein 5 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:22210510 1331961 Arl6ip5 ADP-ribosylation factor-like 6 interacting protein 5 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22461904 1331961 Arl6ip5 ADP-ribosylation factor-like 6 interacting protein 5 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:22210510 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160915 MGI PMID:24813896 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160915 MGI PMID:24813896 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20160519 MGI PMID:26445298 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20160519 MGI PMID:26445298 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:21926268 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20160915 MGI PMID:24813896 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20160915 MGI PMID:24813896 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20665729 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:21926268 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20160519 MGI PMID:26445298 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20160519 MGI PMID:26445298 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:20040596 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0011016 increased core body temperature IAGP N RGD:5509061 20160915 MGI PMID:24813896 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20160915 MGI PMID:24813896 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:20040596 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20160519 MGI PMID:26445298 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20160915 MGI PMID:24813896 1331963 Appl1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 gene MP:0020101 abnormal hepatic glucose production IAGP N RGD:5509061 20160915 MGI PMID:24813896 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:11376114 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:11376114 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:18209067 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210128 MGI 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200310 MGI PMID:10407043 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20200310 MGI PMID:11376114 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:18209067 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:10407043 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0001921 reduced fertility IAGP N RGD:5509061 20200310 MGI PMID:18209067 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:11376114 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:18209067 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:10407043 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20210128 MGI 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:11376114 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:11376114 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:11376114 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20210128 MGI 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20200310 MGI PMID:11376114 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20200310 MGI PMID:11376114 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20200310 MGI PMID:11376114 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:11376114 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20200310 MGI PMID:10407043 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210520 MGI 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210520 MGI 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210520 MGI 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210128 MGI 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20200310 MGI PMID:11376114 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20200310 MGI PMID:11376114 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18209067 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1331966 Npepps aminopeptidase puromycin sensitive gene MP:0030610 absent teeth IEA N RGD:5509061 20210520 MGI 1331969 Oser1 oxidative stress responsive serine rich 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1331969 Oser1 oxidative stress responsive serine rich 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 1331969 Oser1 oxidative stress responsive serine rich 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1331971 Ptpn23 protein tyrosine phosphatase, non-receptor type 23 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160421 MGI 1331971 Ptpn23 protein tyrosine phosphatase, non-receptor type 23 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1331971 Ptpn23 protein tyrosine phosphatase, non-receptor type 23 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19378249 1331971 Ptpn23 protein tyrosine phosphatase, non-receptor type 23 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20160421 MGI 1331971 Ptpn23 protein tyrosine phosphatase, non-receptor type 23 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19378249 1331971 Ptpn23 protein tyrosine phosphatase, non-receptor type 23 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1331972 Acad9 acyl-Coenzyme A dehydrogenase family, member 9 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20221117 MGI PMID:34556413 1331972 Acad9 acyl-Coenzyme A dehydrogenase family, member 9 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20221117 MGI PMID:34556413 1331972 Acad9 acyl-Coenzyme A dehydrogenase family, member 9 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20221117 MGI PMID:34556413 1331972 Acad9 acyl-Coenzyme A dehydrogenase family, member 9 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20221117 MGI PMID:34556413 1331972 Acad9 acyl-Coenzyme A dehydrogenase family, member 9 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20221117 MGI PMID:34556413 1331972 Acad9 acyl-Coenzyme A dehydrogenase family, member 9 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20221117 MGI PMID:34556413 1331972 Acad9 acyl-Coenzyme A dehydrogenase family, member 9 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20221117 MGI PMID:34556413 1331972 Acad9 acyl-Coenzyme A dehydrogenase family, member 9 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20221117 MGI PMID:34556413 1331972 Acad9 acyl-Coenzyme A dehydrogenase family, member 9 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20221117 MGI PMID:34556413 1331972 Acad9 acyl-Coenzyme A dehydrogenase family, member 9 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20221117 MGI PMID:34556413 1331972 Acad9 acyl-Coenzyme A dehydrogenase family, member 9 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20221117 MGI PMID:34556413 1331972 Acad9 acyl-Coenzyme A dehydrogenase family, member 9 gene MP:0012552 lactic acidosis IAGP N RGD:5509061 20221117 MGI PMID:34556413 1331972 Acad9 acyl-Coenzyme A dehydrogenase family, member 9 gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20221117 MGI PMID:34556413 1331973 Scgb3a1 secretoglobin, family 3A, member 1 gene MP:0011053 decreased respiratory motile cilia number IAGP N RGD:5509061 20210204 MGI PMID:30768367 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16207730 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:20454682 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:20454682 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:16207730 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:16207730 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:16207730 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:16517118 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:16517118 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0000568 ectopic digits IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0000580 deformed nails IAGP N RGD:5509061 20141003 MGI PMID:16517118 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22794264 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20454682 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:22794264 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:23986861 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001054 failure of neuromuscular synapse presynaptic differentiation IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001054 failure of neuromuscular synapse presynaptic differentiation IAGP N RGD:5509061 20141003 MGI PMID:23986861 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001055 failure of neuromuscular synapse postsynaptic differentiation IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001055 failure of neuromuscular synapse postsynaptic differentiation IAGP N RGD:5509061 20141003 MGI PMID:23986861 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16517118 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:16517118 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:16517118 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:16517118 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:22794264 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001678 thick apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:16207730 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:16207730 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001921 reduced fertility IEA N RGD:5509061 20151015 MGI 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23986861 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20151015 MGI 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:16207730 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20111116 MGI 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:16517118 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:20018657 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0002772 brachypodia IAGP N RGD:5509061 20230824 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20141003 MGI PMID:22794264 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:20454682 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20141003 MGI PMID:16517118 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0004149 increased bone strength IAGP N RGD:5509061 20200430 MGI PMID:28477420 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20151015 MGI 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0004639 fused metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0004642 fused metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:22794264 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:20454682 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:16207730 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:20018657 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:20454682 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0006369 supernumerary incisors IAGP N RGD:5509061 20141003 MGI PMID:20018657 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20200430 MGI PMID:28477420 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0008730 fused phalanges IEA N RGD:5509061 20151015 MGI 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20200430 MGI PMID:28477420 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20200430 MGI PMID:28477420 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20200430 MGI PMID:28477420 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:23986861 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20200430 MGI PMID:28477420 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20200430 MGI PMID:28477420 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0010932 increased trabecular bone connectivity density IAGP N RGD:5509061 20200430 MGI PMID:28477420 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:20454682 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22794264 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23986861 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20454682 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22794264 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23986861 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16207730 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23986861 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0011298 ureter hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20454682 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0011387 absent metanephric mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:20454682 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0013623 increased femur compact bone thickness IAGP N RGD:5509061 20200430 MGI PMID:28477420 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20200430 MGI PMID:28477420 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0013785 abnormal mammary gland bud morphology IAGP N RGD:5509061 20150611 MGI PMID:17119023 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20200430 MGI PMID:28477420 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0030278 thick neurocranium IAGP N RGD:5509061 20200430 MGI PMID:28477420 1331974 Lrp4 low density lipoprotein receptor-related protein 4 gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20171221 MGI PMID:20018657 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0000371 diluted coat color IAGP N RGD:5509061 20180719 MGI PMID:10470087 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0000371 diluted coat color IAGP N RGD:5509061 20180719 MGI PMID:15070780 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20180719 MGI PMID:17095588 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001257 increased body length IAGP N RGD:5509061 20180719 MGI PMID:10470087 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001257 increased body length IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001257 increased body length IAGP N RGD:5509061 20190328 MGI PMID:29226825 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001260 increased body weight IAGP N RGD:5509061 20180719 MGI PMID:12697680 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001260 increased body weight IAGP N RGD:5509061 20180719 MGI PMID:12834911 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001260 increased body weight IAGP N RGD:5509061 20180719 MGI PMID:16887279 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001260 increased body weight IAGP N RGD:5509061 20180719 MGI PMID:17095588 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001260 increased body weight IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001260 increased body weight IAGP N RGD:5509061 20180719 MGI PMID:8633004 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001260 increased body weight IAGP N RGD:5509061 20190328 MGI PMID:29226825 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001261 obese IAGP N RGD:5509061 20180719 MGI PMID:10470087 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001261 obese IAGP N RGD:5509061 20180719 MGI PMID:12697680 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001261 obese IAGP N RGD:5509061 20180719 MGI PMID:15070780 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001261 obese IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20180719 MGI PMID:12834911 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001425 abnormal alcohol consumption IAGP N RGD:5509061 20180719 MGI PMID:9726280 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001433 polyphagia IAGP N RGD:5509061 20180719 MGI PMID:12697680 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001433 polyphagia IAGP N RGD:5509061 20180719 MGI PMID:15070780 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001433 polyphagia IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001433 polyphagia IAGP N RGD:5509061 20190328 MGI PMID:29226825 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20180719 MGI PMID:12834911 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20180719 MGI PMID:17095588 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20180719 MGI PMID:17095588 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20180719 MGI PMID:10470087 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20180719 MGI PMID:8633004 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20180719 MGI PMID:17095588 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180719 MGI PMID:12697680 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20180719 MGI PMID:9726280 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002664 decreased circulating adrenocorticotropin level IAGP N RGD:5509061 20180719 MGI PMID:10470087 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002664 decreased circulating adrenocorticotropin level IAGP N RGD:5509061 20180719 MGI PMID:12458044 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002664 decreased circulating adrenocorticotropin level IAGP N RGD:5509061 20180719 MGI PMID:17095588 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20180719 MGI PMID:10470087 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20180719 MGI PMID:12458044 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20180719 MGI PMID:15070780 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20180719 MGI PMID:17095588 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20180719 MGI PMID:10470087 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20180719 MGI PMID:17095588 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20180719 MGI PMID:9726280 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0003136 yellow coat color IAGP N RGD:5509061 20180719 MGI PMID:10470087 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0003136 yellow coat color IAGP N RGD:5509061 20180719 MGI PMID:17652101 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20180719 MGI PMID:9726280 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20180719 MGI PMID:12697680 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20180719 MGI PMID:17095588 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20180719 MGI PMID:16887279 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20180719 MGI PMID:17467916 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005128 decreased adrenocorticotropin level IAGP N RGD:5509061 20180719 MGI PMID:17095588 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20180719 MGI PMID:15070780 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20190328 MGI PMID:29226825 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180719 MGI PMID:12697680 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20180719 MGI PMID:10470087 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20180719 MGI PMID:15070780 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180719 MGI PMID:10470087 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180719 MGI PMID:15070780 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005661 decreased circulating adrenaline level IAGP N RGD:5509061 20180719 MGI PMID:10470087 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20180719 MGI PMID:10470087 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20180719 MGI PMID:12697680 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20180719 MGI PMID:12697680 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20180719 MGI PMID:16887279 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0006370 abnormal hair follicle pheomelanosome pheomelanin content IAGP N RGD:5509061 20180719 MGI PMID:17652101 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20180719 MGI PMID:12458044 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20180719 MGI PMID:12458044 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20180719 MGI PMID:12458044 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180719 MGI PMID:12697680 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20180719 MGI PMID:12697680 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20180719 MGI PMID:12697680 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20180719 MGI PMID:12697680 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20180719 MGI PMID:12697680 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20180719 MGI PMID:12458044 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20180719 MGI PMID:17467916 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20180719 MGI PMID:8633004 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20180719 MGI PMID:12697680 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:17095588 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:10470087 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0011939 increased food intake IAGP N RGD:5509061 20180719 MGI PMID:10470087 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0011940 decreased food intake IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20180719 MGI PMID:23093774 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20190328 MGI PMID:29226825 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0014285 disorganized adrenal gland zona fasciculata IAGP N RGD:5509061 20230907 MGI PMID:17095588 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0014286 increased adrenal gland zona fasciculata size IAGP N RGD:5509061 20230907 MGI PMID:17095588 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0014287 decreased adrenal gland zona fasciculata size IAGP N RGD:5509061 20230907 MGI PMID:17095588 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0014441 decreased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:15070780 1331975 Pomc pro-opiomelanocortin-alpha gene MP:0030770 increased urine adrenaline level IAGP N RGD:5509061 20180927 MGI PMID:16887279 1331976 Chct1 CHD1 helical C-terminal domain containing 1 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20230720 MGI 1331976 Chct1 CHD1 helical C-terminal domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0000440 domed cranium IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20141003 MGI 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0000644 dextrocardia IEA N RGD:5509061 20141003 MGI 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0000690 absent spleen IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20141003 MGI 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0001893 non-obstructive hydrocephaly IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0002766 situs inversus IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210520 MGI 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210520 MGI 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0011055 abnormal respiratory motile cilium physiology IEA N RGD:5509061 20141003 MGI 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220519 MGI 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0011252 situs inversus totalis IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0011253 situs inversus with levocardia IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0011649 immotile respiratory cilia IEA N RGD:5509061 20141003 MGI 1331977 Odad3 outer dynein arm docking complex subunit 3 gene MP:0012139 increased forebrain size IAGP N RGD:5509061 20191003 MGI PMID:31383820 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20151203 MGI PMID:24049736 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17090215 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17360356 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17360356 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17360356 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17090215 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17090215 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17090215 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17360356 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17360356 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17090215 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17090215 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200917 MGI PMID:17360356 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0003916 decreased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:20519122 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17090215 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:17090215 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17090215 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17141629 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17090215 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:17141629 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:17141629 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20151203 MGI PMID:24049736 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:20519122 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20151203 MGI PMID:24049736 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:17090215 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20151203 MGI PMID:24049736 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0009137 decreased brown fat lipid droplet number IAGP N RGD:5509061 20151203 MGI PMID:24049736 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17090215 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17141629 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20200917 MGI PMID:17360356 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20151203 MGI PMID:24049736 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20151203 MGI PMID:24049736 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20151203 MGI PMID:24049736 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:17360356 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17360356 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:18628400 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:17090215 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0014344 abnormal skeletal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:17090215 1331978 Ppargc1b peroxisome proliferative activated receptor, gamma, coactivator 1 beta gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:17360356 1331979 Tlr5 toll-like receptor 5 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16891416 1331979 Tlr5 toll-like receptor 5 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0001260 increased body weight IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0001433 polyphagia IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:16891416 1331979 Tlr5 toll-like receptor 5 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0002083 premature death IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16891416 1331979 Tlr5 toll-like receptor 5 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16829963 1331979 Tlr5 toll-like receptor 5 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16891416 1331979 Tlr5 toll-like receptor 5 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16648852 1331979 Tlr5 toll-like receptor 5 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0002816 colitis IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16891416 1331979 Tlr5 toll-like receptor 5 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:21458307 1331979 Tlr5 toll-like receptor 5 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:16891416 1331979 Tlr5 toll-like receptor 5 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:16829963 1331979 Tlr5 toll-like receptor 5 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:16829963 1331979 Tlr5 toll-like receptor 5 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20141003 MGI PMID:20203013 1331979 Tlr5 toll-like receptor 5 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160324 MGI PMID:25172014 1331979 Tlr5 toll-like receptor 5 gene MP:0031342 increased circulating lipocalin 2 level IAGP N RGD:5509061 20220120 MGI PMID:20203013 1331981 Cacybp calcyclin binding protein gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 1331981 Cacybp calcyclin binding protein gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16413921 1331981 Cacybp calcyclin binding protein gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16413921 1331981 Cacybp calcyclin binding protein gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16413921 1331981 Cacybp calcyclin binding protein gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:16413921 1331981 Cacybp calcyclin binding protein gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1331981 Cacybp calcyclin binding protein gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:16413921 1331981 Cacybp calcyclin binding protein gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16413921 1331981 Cacybp calcyclin binding protein gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1331981 Cacybp calcyclin binding protein gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:16413921 1331981 Cacybp calcyclin binding protein gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:16413921 1331982 Cacna2d3 calcium channel, voltage-dependent, alpha2/delta subunit 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20111116 MGI 1331982 Cacna2d3 calcium channel, voltage-dependent, alpha2/delta subunit 3 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20111116 MGI 1331982 Cacna2d3 calcium channel, voltage-dependent, alpha2/delta subunit 3 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21074052 1331982 Cacna2d3 calcium channel, voltage-dependent, alpha2/delta subunit 3 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20240523 MGI 1331982 Cacna2d3 calcium channel, voltage-dependent, alpha2/delta subunit 3 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20240523 MGI 1331982 Cacna2d3 calcium channel, voltage-dependent, alpha2/delta subunit 3 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:21074052 1331982 Cacna2d3 calcium channel, voltage-dependent, alpha2/delta subunit 3 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:21074052 1331982 Cacna2d3 calcium channel, voltage-dependent, alpha2/delta subunit 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1331982 Cacna2d3 calcium channel, voltage-dependent, alpha2/delta subunit 3 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1331982 Cacna2d3 calcium channel, voltage-dependent, alpha2/delta subunit 3 gene MP:0005655 increased aggression IEA N RGD:5509061 20111116 MGI 1331983 Kcnmb2 potassium large conductance calcium-activated channel, subfamily M, beta member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151119 MGI PMID:25267913 1331983 Kcnmb2 potassium large conductance calcium-activated channel, subfamily M, beta member 2 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20151119 MGI PMID:25267913 1331983 Kcnmb2 potassium large conductance calcium-activated channel, subfamily M, beta member 2 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20151119 MGI PMID:25267913 1331983 Kcnmb2 potassium large conductance calcium-activated channel, subfamily M, beta member 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20151119 MGI PMID:25267913 1331984 Sat1 spermidine/spermine N1-acetyl transferase 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20200310 MGI PMID:17189273 1331984 Sat1 spermidine/spermine N1-acetyl transferase 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:17189273 1331984 Sat1 spermidine/spermine N1-acetyl transferase 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:15958588 1331984 Sat1 spermidine/spermine N1-acetyl transferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15958588 1331984 Sat1 spermidine/spermine N1-acetyl transferase 1 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20200310 MGI PMID:17189273 1331984 Sat1 spermidine/spermine N1-acetyl transferase 1 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20200310 MGI PMID:17189273 1331984 Sat1 spermidine/spermine N1-acetyl transferase 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:17189273 1331984 Sat1 spermidine/spermine N1-acetyl transferase 1 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20200310 MGI PMID:17189273 1331984 Sat1 spermidine/spermine N1-acetyl transferase 1 gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:17189273 1331984 Sat1 spermidine/spermine N1-acetyl transferase 1 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20200310 MGI PMID:17189273 1331985 Timm13 translocase of inner mitochondrial membrane 13 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20190502 MGI 1331985 Timm13 translocase of inner mitochondrial membrane 13 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1331985 Timm13 translocase of inner mitochondrial membrane 13 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20190502 MGI 1331985 Timm13 translocase of inner mitochondrial membrane 13 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20190502 MGI 1331985 Timm13 translocase of inner mitochondrial membrane 13 gene MP:0002637 small uterus IEA N RGD:5509061 20190502 MGI 1331985 Timm13 translocase of inner mitochondrial membrane 13 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20190502 MGI 1331985 Timm13 translocase of inner mitochondrial membrane 13 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20190502 MGI 1331985 Timm13 translocase of inner mitochondrial membrane 13 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1331985 Timm13 translocase of inner mitochondrial membrane 13 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20210826 MGI 1331986 Fam162a family with sequence similarity 162, member A gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 1331986 Fam162a family with sequence similarity 162, member A gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1331986 Fam162a family with sequence similarity 162, member A gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1331986 Fam162a family with sequence similarity 162, member A gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1331986 Fam162a family with sequence similarity 162, member A gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1331986 Fam162a family with sequence similarity 162, member A gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20181227 MGI 1331986 Fam162a family with sequence similarity 162, member A gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1331986 Fam162a family with sequence similarity 162, member A gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21669879 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:18566297 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:19286635 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21669879 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:18566297 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18566297 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:19286635 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21669879 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21669879 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21669879 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:19286635 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20170824 MGI PMID:25667419 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19286635 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21669879 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:21669879 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21669879 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20141003 MGI PMID:19286635 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20170824 MGI PMID:25605874 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20170824 MGI PMID:25667419 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19286635 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0010163 hemolysis IAGP N RGD:5509061 20141003 MGI PMID:19286635 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20170824 MGI PMID:25605874 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20170824 MGI PMID:25667419 1331987 Sgms2 sphingomyelin synthase 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:21669879 1331988 Dpysl5 dihydropyrimidinase-like 5 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:21289187 1331988 Dpysl5 dihydropyrimidinase-like 5 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:21289187 1331988 Dpysl5 dihydropyrimidinase-like 5 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21289187 1331988 Dpysl5 dihydropyrimidinase-like 5 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:21289187 1331988 Dpysl5 dihydropyrimidinase-like 5 gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:21289187 1331989 Klb klotho beta gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23209629 1331989 Klb klotho beta gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23209629 1331989 Klb klotho beta gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:16075061 1331989 Klb klotho beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16075061 1331989 Klb klotho beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23209629 1331989 Klb klotho beta gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210520 MGI 1331989 Klb klotho beta gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23209629 1331989 Klb klotho beta gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210520 MGI 1331989 Klb klotho beta gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0003457 abnormal circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:23209629 1331989 Klb klotho beta gene MP:0003959 abnormal lean body mass IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20210520 MGI 1331989 Klb klotho beta gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23209629 1331989 Klb klotho beta gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16075061 1331989 Klb klotho beta gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:23209629 1331989 Klb klotho beta gene MP:0005457 abnormal percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0005667 abnormal circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23209629 1331989 Klb klotho beta gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0005675 small gallbladder IAGP N RGD:5509061 20141003 MGI PMID:16075061 1331989 Klb klotho beta gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220519 MGI 1331989 Klb klotho beta gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:23209629 1331989 Klb klotho beta gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1331989 Klb klotho beta gene MP:0012320 abnormal body fat mass IAGP N RGD:5509061 20160407 MGI PMID:23209629 1331989 Klb klotho beta gene MP:0030967 abnormal circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:23209629 1331989 Klb klotho beta gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:22958921 1331989 Klb klotho beta gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:22958921 1331990 Csnk1g3 casein kinase 1, gamma 3 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20240627 MGI 1331990 Csnk1g3 casein kinase 1, gamma 3 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20201022 MGI 1331990 Csnk1g3 casein kinase 1, gamma 3 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20170105 MGI 1331990 Csnk1g3 casein kinase 1, gamma 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1331990 Csnk1g3 casein kinase 1, gamma 3 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20200402 MGI 1331990 Csnk1g3 casein kinase 1, gamma 3 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1331990 Csnk1g3 casein kinase 1, gamma 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1331990 Csnk1g3 casein kinase 1, gamma 3 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20200402 MGI 1331990 Csnk1g3 casein kinase 1, gamma 3 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20201231 MGI 1331990 Csnk1g3 casein kinase 1, gamma 3 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1331990 Csnk1g3 casein kinase 1, gamma 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0000292 distended pericardium IEA N RGD:5509061 20191128 MGI 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0000929 open neural tube IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20181227 MGI 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0002861 abnormal tail bud morphology IEA N RGD:5509061 20181227 MGI 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20181227 MGI 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20181227 MGI 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0013214 decreased embryonic neuroepithelium primary cilium number IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1331996 Ppp1r35 protein phosphatase 1, regulatory subunit 35 gene MP:0030538 abnormal notochordal plate morphology IAGP N RGD:5509061 20240620 MGI PMID:32628936 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0001394 circling IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0003169 abnormal scala media morphology IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0004317 small vestibular saccule IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0004330 abnormal vestibular saccular macula morphology IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0008307 short scala media IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0008308 small scala media IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0009259 abnormal vestibular saccule duct morphology IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331997 Mctp1 multiple C2 domains, transmembrane 1 gene MP:0013911 fused vestibular saccule and utricle IAGP N RGD:5509061 20181220 MGI PMID:30217595 1331998 Tmem86a transmembrane protein 86A gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1331998 Tmem86a transmembrane protein 86A gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1331998 Tmem86a transmembrane protein 86A gene MP:0002764 short tibia IEA N RGD:5509061 20231207 MGI 1331998 Tmem86a transmembrane protein 86A gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:14716005 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:14716005 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:14716005 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:14716005 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20200409 MGI PMID:30976389 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14716005 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200409 MGI PMID:30976389 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20200409 MGI PMID:30976389 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:14716005 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200409 MGI PMID:30976389 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:14716005 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14716005 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200409 MGI PMID:30976389 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:14716005 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16926188 1332001 Ss18l1 SS18, nBAF chromatin remodeling complex subunit like 1 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20200409 MGI PMID:30976389 1332002 Dnase2b deoxyribonuclease II beta gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 1332002 Dnase2b deoxyribonuclease II beta gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:12944971 1332002 Dnase2b deoxyribonuclease II beta gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1332002 Dnase2b deoxyribonuclease II beta gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:12944971 1332002 Dnase2b deoxyribonuclease II beta gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12944971 1332003 Vwce von Willebrand factor C and EGF domains gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230119 MGI 1332003 Vwce von Willebrand factor C and EGF domains gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230119 MGI 1332003 Vwce von Willebrand factor C and EGF domains gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230119 MGI 1332004 Pgp phosphoglycolate phosphatase gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20180426 MGI PMID:27731369 1332004 Pgp phosphoglycolate phosphatase gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20180426 MGI PMID:27731369 1332004 Pgp phosphoglycolate phosphatase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180426 MGI PMID:27731369 1332004 Pgp phosphoglycolate phosphatase gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20180426 MGI PMID:27731369 1332004 Pgp phosphoglycolate phosphatase gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20180426 MGI PMID:27731369 1332004 Pgp phosphoglycolate phosphatase gene MP:0001914 hemorrhage IAGP N RGD:5509061 20180426 MGI PMID:27731369 1332004 Pgp phosphoglycolate phosphatase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180426 MGI PMID:27731369 1332004 Pgp phosphoglycolate phosphatase gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20180426 MGI PMID:27731369 1332004 Pgp phosphoglycolate phosphatase gene MP:0004259 small placenta IAGP N RGD:5509061 20180426 MGI PMID:27731369 1332004 Pgp phosphoglycolate phosphatase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20180426 MGI PMID:27731369 1332004 Pgp phosphoglycolate phosphatase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180426 MGI PMID:27731369 1332004 Pgp phosphoglycolate phosphatase gene MP:0011702 abnormal fibroblast proliferation IAGP N RGD:5509061 20180426 MGI PMID:27731369 1332005 Svop SV2 related protein gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 1332005 Svop SV2 related protein gene MP:0001523 impaired righting response IEA N RGD:5509061 20201022 MGI 1332005 Svop SV2 related protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23894296 1332005 Svop SV2 related protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23894296 1332005 Svop SV2 related protein gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1332005 Svop SV2 related protein gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1332005 Svop SV2 related protein gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23894296 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:17584971 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:15030763 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:15030763 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:15030763 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17584971 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19838304 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:19838304 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:19838304 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19838304 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22366455 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:22366455 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:22366455 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15030763 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15030763 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141204 MGI PMID:25102060 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001705 abnormal proximal-distal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15030763 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141016 MGI PMID:24361262 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141016 MGI PMID:24361262 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141016 MGI PMID:24361262 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15030763 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17584971 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141204 MGI PMID:25102060 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:15030763 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:17584971 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15030763 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19838304 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:15030763 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20231207 MGI PMID:35364055 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:22366455 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:22366455 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0003958 heart valve hyperplasia IAGP N RGD:5509061 20231207 MGI PMID:35364055 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:17584971 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:19838304 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:19838304 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141204 MGI PMID:25102060 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:22366455 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17584971 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20141003 MGI PMID:22366455 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0009603 absent keratohyalin granules IAGP N RGD:5509061 20141003 MGI PMID:22366455 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0010197 abnormal lymphatic vessel endothelial cell morphology IAGP N RGD:5509061 20141016 MGI PMID:24361262 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231207 MGI PMID:35364055 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0010591 enlarged aortic valve IAGP N RGD:5509061 20231207 MGI PMID:35364055 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20231207 MGI PMID:35364055 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0010595 abnormal aortic valve cusp morphology IAGP N RGD:5509061 20231207 MGI PMID:35364055 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15030763 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17584971 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141204 MGI PMID:25102060 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0011233 abnormal vitamin A metabolism IAGP N RGD:5509061 20231207 MGI PMID:35364055 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0014106 delayed chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:15030763 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:15030763 1332006 Cyp26b1 cytochrome P450, family 26, subfamily b, polypeptide 1 gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:15030763 1332007 Ccdc124 coiled-coil domain containing 124 gene MP:0000601 small liver IEA N RGD:5509061 20170105 MGI 1332007 Ccdc124 coiled-coil domain containing 124 gene MP:0000692 small spleen IEA N RGD:5509061 20170105 MGI 1332007 Ccdc124 coiled-coil domain containing 124 gene MP:0000774 decreased brain size IEA N RGD:5509061 20170105 MGI 1332007 Ccdc124 coiled-coil domain containing 124 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1332007 Ccdc124 coiled-coil domain containing 124 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1332007 Ccdc124 coiled-coil domain containing 124 gene MP:0002188 small heart IEA N RGD:5509061 20170105 MGI 1332007 Ccdc124 coiled-coil domain containing 124 gene MP:0003641 small lung IEA N RGD:5509061 20170105 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17327425 1332010 Adipor1 adiponectin receptor 1 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17327425 1332010 Adipor1 adiponectin receptor 1 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17268472 1332010 Adipor1 adiponectin receptor 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20160421 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20201022 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17327425 1332010 Adipor1 adiponectin receptor 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210128 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17268472 1332010 Adipor1 adiponectin receptor 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17268472 1332010 Adipor1 adiponectin receptor 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20357764 1332010 Adipor1 adiponectin receptor 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17268472 1332010 Adipor1 adiponectin receptor 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20357764 1332010 Adipor1 adiponectin receptor 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17327425 1332010 Adipor1 adiponectin receptor 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20201022 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:17268472 1332010 Adipor1 adiponectin receptor 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:20357764 1332010 Adipor1 adiponectin receptor 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20181227 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20211021 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:17327425 1332010 Adipor1 adiponectin receptor 1 gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20180111 MGI PMID:24531262 1332010 Adipor1 adiponectin receptor 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17327425 1332010 Adipor1 adiponectin receptor 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:20357764 1332010 Adipor1 adiponectin receptor 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17268472 1332010 Adipor1 adiponectin receptor 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17327425 1332010 Adipor1 adiponectin receptor 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17268472 1332010 Adipor1 adiponectin receptor 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:20357764 1332010 Adipor1 adiponectin receptor 1 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:17327425 1332010 Adipor1 adiponectin receptor 1 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17327425 1332010 Adipor1 adiponectin receptor 1 gene MP:0005543 decreased cornea thickness IEA N RGD:5509061 20181227 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17268472 1332010 Adipor1 adiponectin receptor 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20357764 1332010 Adipor1 adiponectin receptor 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17268472 1332010 Adipor1 adiponectin receptor 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17327425 1332010 Adipor1 adiponectin receptor 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17268472 1332010 Adipor1 adiponectin receptor 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17327425 1332010 Adipor1 adiponectin receptor 1 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:20357764 1332010 Adipor1 adiponectin receptor 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0011019 abnormal adaptive thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:24531262 1332010 Adipor1 adiponectin receptor 1 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:24531262 1332010 Adipor1 adiponectin receptor 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20181227 MGI 1332010 Adipor1 adiponectin receptor 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:20357764 1332010 Adipor1 adiponectin receptor 1 gene MP:0014344 abnormal skeletal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:20357764 1332010 Adipor1 adiponectin receptor 1 gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:24531262 1332010 Adipor1 adiponectin receptor 1 gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:20357764 1332011 Amdhd2 amidohydrolase domain containing 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20220519 MGI PMID:35229715 1332012 Efcab6 EF-hand calcium binding domain 6 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220519 MGI 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160114 MGI PMID:9636176 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20160114 MGI PMID:15755804 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20221215 MGI 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0005083 abnormal biliary tract morphology IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20160114 MGI PMID:9636176 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20160114 MGI PMID:9636176 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20160114 MGI PMID:15755804 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0012183 decreased paraxial mesoderm size IAGP N RGD:5509061 20160114 MGI PMID:15755804 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0012183 decreased paraxial mesoderm size IAGP N RGD:5509061 20160114 MGI PMID:9636176 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0012254 absent intersomitic vessels IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0012272 decreased axial mesoderm size IAGP N RGD:5509061 20160114 MGI PMID:15755804 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0012498 abnormal cardiogenic plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21490058 1332013 Poglut1 protein O-glucosyltransferase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1332015 Tmub1 transmembrane and ubiquitin-like domain containing 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20141003 MGI 1332015 Tmub1 transmembrane and ubiquitin-like domain containing 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220428 MGI 1332015 Tmub1 transmembrane and ubiquitin-like domain containing 1 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:20582322 1332015 Tmub1 transmembrane and ubiquitin-like domain containing 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20201210 MGI PMID:31867855 1332015 Tmub1 transmembrane and ubiquitin-like domain containing 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20201210 MGI PMID:31867855 1332015 Tmub1 transmembrane and ubiquitin-like domain containing 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20201210 MGI PMID:31867855 1332015 Tmub1 transmembrane and ubiquitin-like domain containing 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20201210 MGI PMID:31867855 1332015 Tmub1 transmembrane and ubiquitin-like domain containing 1 gene MP:0008853 decreased abdominal adipose tissue amount IEA N RGD:5509061 20141003 MGI 1332015 Tmub1 transmembrane and ubiquitin-like domain containing 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20201210 MGI PMID:31867855 1332015 Tmub1 transmembrane and ubiquitin-like domain containing 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20141003 MGI 1332015 Tmub1 transmembrane and ubiquitin-like domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20201210 MGI PMID:31867855 1332015 Tmub1 transmembrane and ubiquitin-like domain containing 1 gene MP:0021198 abnormal sleep duration IAGP N RGD:5509061 20220922 MGI PMID:20582322 1332015 Tmub1 transmembrane and ubiquitin-like domain containing 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:20582322 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0000111 cleft palate IAGP N RGD:5509061 20220630 MGI PMID:34302166 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20230601 MGI 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180607 MGI PMID:26787558 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0000914 exencephaly IAGP N RGD:5509061 20220630 MGI PMID:34302166 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20180607 MGI PMID:26787558 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0003052 omphalocele IAGP N RGD:5509061 20220630 MGI PMID:34302166 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20180607 MGI PMID:26787558 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20220630 MGI PMID:34302166 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0005262 coloboma IAGP N RGD:5509061 20220630 MGI PMID:34302166 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20180607 MGI PMID:26787558 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20220630 MGI PMID:34302166 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221027 MGI PMID:33446878 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20220630 MGI PMID:34302166 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221027 MGI PMID:33446878 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20180607 MGI PMID:26787558 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180607 MGI PMID:26787558 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20220630 MGI PMID:34302166 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0012746 abnormal neural crest cell delamination IAGP N RGD:5509061 20180607 MGI PMID:26787558 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0012757 abnormal cranial neural crest cell migration IAGP N RGD:5509061 20180607 MGI PMID:26787558 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0013818 abnormal oral cavity morphology IAGP N RGD:5509061 20220630 MGI PMID:34302166 1332016 Specc1l sperm antigen with calponin homology and coiled-coil domains 1-like gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20221027 MGI PMID:33446878 1332017 G6pc3 glucose 6 phosphatase, catalytic, 3 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17318259 1332017 G6pc3 glucose 6 phosphatase, catalytic, 3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:17318259 1332017 G6pc3 glucose 6 phosphatase, catalytic, 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17023421 1332017 G6pc3 glucose 6 phosphatase, catalytic, 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17023421 1332017 G6pc3 glucose 6 phosphatase, catalytic, 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17023421 1332017 G6pc3 glucose 6 phosphatase, catalytic, 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17318259 1332017 G6pc3 glucose 6 phosphatase, catalytic, 3 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17318259 1332017 G6pc3 glucose 6 phosphatase, catalytic, 3 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:17023421 1332017 G6pc3 glucose 6 phosphatase, catalytic, 3 gene MP:0005074 impaired granulocyte bactericidal activity IAGP N RGD:5509061 20141003 MGI PMID:17318259 1332017 G6pc3 glucose 6 phosphatase, catalytic, 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17023421 1332017 G6pc3 glucose 6 phosphatase, catalytic, 3 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:17023421 1332017 G6pc3 glucose 6 phosphatase, catalytic, 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17318259 1332018 Kng1 kininogen 1 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20200310 MGI PMID:18000168 1332018 Kng1 kininogen 1 gene MP:0012359 increased partial thromboplastin time IAGP N RGD:5509061 20200924 MGI PMID:18000168 1332018 Kng1 kininogen 1 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:18000168 1332019 Lrr1 leucine rich repeat protein 1 gene MP:0000745 tremors IEA N RGD:5509061 20181227 MGI 1332019 Lrr1 leucine rich repeat protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332019 Lrr1 leucine rich repeat protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20170105 MGI 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20170105 MGI 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20170105 MGI 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:24413433 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:24413433 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:24413433 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:24413433 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:24413433 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:24413433 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:24413433 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:24413433 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20141003 MGI PMID:24413433 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20141003 MGI PMID:24413433 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0013236 ovary degeneration IAGP N RGD:5509061 20141003 MGI PMID:24413433 1332022 Terb1 telomere repeat binding bouquet formation protein 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:24413433 1332023 Tmem79 transmembrane protein 79 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20141003 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0000402 abnormal zigzag hair morphology IEA N RGD:5509061 20120105 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0000403 increased curvature of zigzag hairs IEA N RGD:5509061 20120105 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0000411 shiny fur IEA N RGD:5509061 20120105 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0000416 sparse hair IEA N RGD:5509061 20120105 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0000427 abnormal hair cycle IEA N RGD:5509061 20141003 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0001191 abnormal skin condition IEA N RGD:5509061 20120105 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:24060273 1332023 Tmem79 transmembrane protein 79 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:24060273 1332023 Tmem79 transmembrane protein 79 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:24060273 1332023 Tmem79 transmembrane protein 79 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:24060273 1332023 Tmem79 transmembrane protein 79 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20141003 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20120105 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:24060273 1332023 Tmem79 transmembrane protein 79 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0003809 abnormal hair shaft morphology IEA N RGD:5509061 20141003 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0003846 matted coat IAGP N RGD:5509061 20141003 MGI PMID:24060273 1332023 Tmem79 transmembrane protein 79 gene MP:0003846 matted coat IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0003848 brittle hair IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0005409 darkened coat color IEA N RGD:5509061 20141003 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0009801 abnormal hair cortex keratinization IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:24084074 1332023 Tmem79 transmembrane protein 79 gene MP:0010686 abnormal hair follicle matrix region morphology IEA N RGD:5509061 20141003 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20170105 MGI 1332023 Tmem79 transmembrane protein 79 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1332024 Pla1a phospholipase A1 member A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20230601 MGI PMID:35955693 1332024 Pla1a phospholipase A1 member A gene MP:0001265 decreased body size IAGP N RGD:5509061 20230601 MGI PMID:35955693 1332024 Pla1a phospholipase A1 member A gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20230601 MGI PMID:35955693 1332024 Pla1a phospholipase A1 member A gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20230601 MGI PMID:35955693 1332024 Pla1a phospholipase A1 member A gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20230601 MGI PMID:35955693 1332024 Pla1a phospholipase A1 member A gene MP:0012573 decreased susceptibility to chemically induced skin inflammation IAGP N RGD:5509061 20230601 MGI PMID:35955693 1332026 Trim23 tripartite motif-containing 23 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20240516 MGI PMID:33957127 1332026 Trim23 tripartite motif-containing 23 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20240516 MGI PMID:33957127 1332029 Gpm6a glycoprotein m6a gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:21714103 1332029 Gpm6a glycoprotein m6a gene MP:0005458 increased percent body fat/body weight IEA N RGD:5509061 20111116 MGI 1332032 Il24 interleukin 24 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20170105 MGI 1332032 Il24 interleukin 24 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1332032 Il24 interleukin 24 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 1332032 Il24 interleukin 24 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1332034 Rab15 RAB15, member RAS oncogene family gene MP:0001513 limb grasping IEA N RGD:5509061 20170105 MGI 1332034 Rab15 RAB15, member RAS oncogene family gene MP:0002727 decreased circulating insulin level IEA N RGD:5509061 20211021 MGI 1332035 Crtc2 CREB regulated transcription coactivator 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:19583954 1332035 Crtc2 CREB regulated transcription coactivator 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19583954 1332035 Crtc2 CREB regulated transcription coactivator 2 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:19583954 1332035 Crtc2 CREB regulated transcription coactivator 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20133702 1332035 Crtc2 CREB regulated transcription coactivator 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20133702 1332035 Crtc2 CREB regulated transcription coactivator 2 gene MP:0005439 decreased glycogen level IAGP N RGD:5509061 20141003 MGI PMID:19583954 1332035 Crtc2 CREB regulated transcription coactivator 2 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20200102 MGI PMID:20133702 1332035 Crtc2 CREB regulated transcription coactivator 2 gene MP:0020103 decreased hepatic glucose production IAGP N RGD:5509061 20200102 MGI PMID:20133702 1332035 Crtc2 CREB regulated transcription coactivator 2 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:24898145 1332035 Crtc2 CREB regulated transcription coactivator 2 gene MP:0030973 impaired gluconeogenesis IAGP N RGD:5509061 20200102 MGI PMID:20133702 1332036 Zfp57 zinc finger protein 57 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:18854139 1332036 Zfp57 zinc finger protein 57 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:18854139 1332036 Zfp57 zinc finger protein 57 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18854139 1332036 Zfp57 zinc finger protein 57 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18854139 1332038 Atp6v1f ATPase, H+ transporting, lysosomal V1 subunit F gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1332038 Atp6v1f ATPase, H+ transporting, lysosomal V1 subunit F gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1332038 Atp6v1f ATPase, H+ transporting, lysosomal V1 subunit F gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0000604 amyloidosis IAGP N RGD:5509061 20200310 MGI PMID:16354928 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:22049418 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20200310 MGI PMID:17099708 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20200310 MGI PMID:23792428 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:15987683 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:15987683 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20200310 MGI PMID:14664815 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20200310 MGI PMID:15987683 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20200310 MGI PMID:16354928 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:15987683 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:23792428 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:23792428 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20200310 MGI PMID:14664815 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20200310 MGI PMID:16354928 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20200310 MGI PMID:18385378 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:15987683 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20200310 MGI PMID:16354928 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20200310 MGI PMID:14664815 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:11224535 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:11406613 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15080893 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20200310 MGI PMID:22049418 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0002863 improved righting response IAGP N RGD:5509061 20200310 MGI PMID:14664815 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20200310 MGI PMID:16354928 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20200310 MGI PMID:16354928 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20200310 MGI PMID:16354928 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200310 MGI PMID:22049418 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20200310 MGI PMID:18385378 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20200310 MGI PMID:15987683 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20200310 MGI PMID:15987683 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20200310 MGI PMID:17099708 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:17099708 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20200310 MGI PMID:18385378 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20200310 MGI PMID:23792428 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20200310 MGI PMID:15987683 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:15824102 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20200310 MGI PMID:16354928 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20200310 MGI PMID:16354928 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20200310 MGI PMID:18385378 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0008486 decreased muscle spindle number IAGP N RGD:5509061 20200310 MGI PMID:23792428 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20200310 MGI PMID:18385378 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:18385378 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20200310 MGI PMID:18385378 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:17099708 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15987683 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0011619 abnormal dishabituation IAGP N RGD:5509061 20200310 MGI PMID:18385378 1332039 Bace1 beta-site APP cleaving enzyme 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:15987683 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0001147 small testis IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20160804 MGI 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:17994007 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:17994007 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17994007 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17994007 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:17994007 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17994007 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0004930 small epididymis IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:17994007 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:17994007 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0006428 ectopic Sertoli cells IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20160804 MGI 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:17994007 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17994007 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0020355 abnormal Sertoli cell barrier morphology IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0020356 abnormal Sertoli cell barrier function IAGP N RGD:5509061 20220616 MGI PMID:35440090 1332040 Uhrf1 ubiquitin-like, containing PHD and RING finger domains, 1 gene MP:0031406 decreased Sertoli cell proliferation IAGP N RGD:5509061 20220630 MGI PMID:35440090 1332043 Ndrg4 N-myc downstream regulated gene 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 1332043 Ndrg4 N-myc downstream regulated gene 4 gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 1332043 Ndrg4 N-myc downstream regulated gene 4 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:21636852 1332043 Ndrg4 N-myc downstream regulated gene 4 gene MP:0001513 limb grasping IEA N RGD:5509061 20160421 MGI 1332043 Ndrg4 N-myc downstream regulated gene 4 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:21636852 1332043 Ndrg4 N-myc downstream regulated gene 4 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:21636852 1332043 Ndrg4 N-myc downstream regulated gene 4 gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20211021 MGI 1332043 Ndrg4 N-myc downstream regulated gene 4 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1332043 Ndrg4 N-myc downstream regulated gene 4 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1332043 Ndrg4 N-myc downstream regulated gene 4 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:21636852 1332044 Cxcl9 C-X-C motif chemokine ligand 9 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20181227 MGI 1332044 Cxcl9 C-X-C motif chemokine ligand 9 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160421 MGI 1332044 Cxcl9 C-X-C motif chemokine ligand 9 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12133969 1332044 Cxcl9 C-X-C motif chemokine ligand 9 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17296171 1332044 Cxcl9 C-X-C motif chemokine ligand 9 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12133969 1332044 Cxcl9 C-X-C motif chemokine ligand 9 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17296171 1332044 Cxcl9 C-X-C motif chemokine ligand 9 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 1332044 Cxcl9 C-X-C motif chemokine ligand 9 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1332044 Cxcl9 C-X-C motif chemokine ligand 9 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 1332045 Tedc2 tubulin epsilon and delta complex 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1332045 Tedc2 tubulin epsilon and delta complex 2 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20201022 MGI 1332045 Tedc2 tubulin epsilon and delta complex 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1332045 Tedc2 tubulin epsilon and delta complex 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1332045 Tedc2 tubulin epsilon and delta complex 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332045 Tedc2 tubulin epsilon and delta complex 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1332046 Ints7 integrator complex subunit 7 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1332046 Ints7 integrator complex subunit 7 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201231 MGI 1332046 Ints7 integrator complex subunit 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332046 Ints7 integrator complex subunit 7 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1332048 Abat 4-aminobutyrate aminotransferase gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20240606 MGI PMID:36192601 1332048 Abat 4-aminobutyrate aminotransferase gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20240606 MGI PMID:36192601 1332048 Abat 4-aminobutyrate aminotransferase gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20240606 MGI PMID:36192601 1332048 Abat 4-aminobutyrate aminotransferase gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20240606 MGI PMID:36192601 1332048 Abat 4-aminobutyrate aminotransferase gene MP:0008397 abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology IAGP N RGD:5509061 20240606 MGI PMID:36192601 1332048 Abat 4-aminobutyrate aminotransferase gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20240606 MGI PMID:36192601 1332048 Abat 4-aminobutyrate aminotransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332049 Dlgap2 DLG associated protein 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230601 MGI 1332049 Dlgap2 DLG associated protein 2 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20180809 MGI PMID:25071926 1332049 Dlgap2 DLG associated protein 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20180809 MGI PMID:25071926 1332049 Dlgap2 DLG associated protein 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1332049 Dlgap2 DLG associated protein 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20180809 MGI PMID:25071926 1332049 Dlgap2 DLG associated protein 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20180809 MGI PMID:25071926 1332049 Dlgap2 DLG associated protein 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20180809 MGI PMID:25071926 1332049 Dlgap2 DLG associated protein 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20230601 MGI 1332049 Dlgap2 DLG associated protein 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20230601 MGI 1332049 Dlgap2 DLG associated protein 2 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20180809 MGI PMID:25071926 1332049 Dlgap2 DLG associated protein 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20180809 MGI PMID:25071926 1332049 Dlgap2 DLG associated protein 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1332049 Dlgap2 DLG associated protein 2 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20180809 MGI PMID:25071926 1332049 Dlgap2 DLG associated protein 2 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20180809 MGI PMID:25071926 1332050 Fgd4 FYVE, RhoGEF and PH domain containing 4 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20211021 MGI 1332050 Fgd4 FYVE, RhoGEF and PH domain containing 4 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:23171661 1332050 Fgd4 FYVE, RhoGEF and PH domain containing 4 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:23171661 1332050 Fgd4 FYVE, RhoGEF and PH domain containing 4 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23171661 1332050 Fgd4 FYVE, RhoGEF and PH domain containing 4 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:23171661 1332050 Fgd4 FYVE, RhoGEF and PH domain containing 4 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:23171661 1332050 Fgd4 FYVE, RhoGEF and PH domain containing 4 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:23171661 1332050 Fgd4 FYVE, RhoGEF and PH domain containing 4 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23171661 1332052 Qrich1 glutamine-rich 1 gene MP:0000111 cleft palate IEA N RGD:5509061 20170209 MGI 1332052 Qrich1 glutamine-rich 1 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20170209 MGI 1332052 Qrich1 glutamine-rich 1 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170209 MGI 1332052 Qrich1 glutamine-rich 1 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20170209 MGI 1332052 Qrich1 glutamine-rich 1 gene MP:0004056 abnormal myocardium compact layer morphology IEA N RGD:5509061 20170209 MGI 1332052 Qrich1 glutamine-rich 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20170209 MGI 1332052 Qrich1 glutamine-rich 1 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20170209 MGI 1332052 Qrich1 glutamine-rich 1 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170209 MGI 1332052 Qrich1 glutamine-rich 1 gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20170209 MGI 1332053 Chn1 chimerin 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17719550 1332053 Chn1 chimerin 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200507 MGI PMID:28346224 1332053 Chn1 chimerin 1 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17785183 1332053 Chn1 chimerin 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:17719550 1332053 Chn1 chimerin 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20150219 MGI PMID:24623763 1332053 Chn1 chimerin 1 gene MP:0001070 abnormal abducens nerve morphology IAGP N RGD:5509061 20200507 MGI PMID:28346224 1332053 Chn1 chimerin 1 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17785183 1332053 Chn1 chimerin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17719550 1332053 Chn1 chimerin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17785182 1332053 Chn1 chimerin 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:17785183 1332053 Chn1 chimerin 1 gene MP:0001396 unidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:17785182 1332053 Chn1 chimerin 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1332053 Chn1 chimerin 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17719550 1332053 Chn1 chimerin 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17785182 1332053 Chn1 chimerin 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17785183 1332053 Chn1 chimerin 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20150219 MGI PMID:24623763 1332053 Chn1 chimerin 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1332053 Chn1 chimerin 1 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1332053 Chn1 chimerin 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200507 MGI PMID:28346224 1332053 Chn1 chimerin 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20150219 MGI 1332053 Chn1 chimerin 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:17785182 1332053 Chn1 chimerin 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20200507 MGI PMID:28346224 1332053 Chn1 chimerin 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17719550 1332053 Chn1 chimerin 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 1332053 Chn1 chimerin 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20231207 MGI 1332053 Chn1 chimerin 1 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20160421 MGI 1332053 Chn1 chimerin 1 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:17785182 1332053 Chn1 chimerin 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20240523 MGI 1332053 Chn1 chimerin 1 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:17719550 1332053 Chn1 chimerin 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1332053 Chn1 chimerin 1 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20211021 MGI 1332053 Chn1 chimerin 1 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20150219 MGI PMID:24623763 1332053 Chn1 chimerin 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:17785182 1332053 Chn1 chimerin 1 gene MP:0003880 abnormal central pattern generator function IAGP N RGD:5509061 20141003 MGI PMID:17785182 1332053 Chn1 chimerin 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160421 MGI 1332053 Chn1 chimerin 1 gene MP:0004100 abnormal spinal cord interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17785183 1332053 Chn1 chimerin 1 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17785183 1332053 Chn1 chimerin 1 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220519 MGI 1332053 Chn1 chimerin 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160421 MGI 1332053 Chn1 chimerin 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 1332053 Chn1 chimerin 1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20211021 MGI 1332053 Chn1 chimerin 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1332053 Chn1 chimerin 1 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20200507 MGI PMID:28346224 1332053 Chn1 chimerin 1 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:17719550 1332053 Chn1 chimerin 1 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:17785183 1332053 Chn1 chimerin 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 1332053 Chn1 chimerin 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1332053 Chn1 chimerin 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332053 Chn1 chimerin 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:17785182 1332053 Chn1 chimerin 1 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20201022 MGI 1332055 Slc4a9 solute carrier family 4, sodium bicarbonate cotransporter, member 9 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17170027 1332055 Slc4a9 solute carrier family 4, sodium bicarbonate cotransporter, member 9 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:23610411 1332056 Hnrnpr heterogeneous nuclear ribonucleoprotein R gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20240425 MGI PMID:34850154 1332056 Hnrnpr heterogeneous nuclear ribonucleoprotein R gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20240425 MGI PMID:34850154 1332057 Rtcb RNA 2',3'-cyclic phosphate and 5'-OH ligase gene MP:0001127 small ovary IAGP N RGD:5509061 20230330 MGI PMID:36178098 1332057 Rtcb RNA 2',3'-cyclic phosphate and 5'-OH ligase gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20151008 MGI PMID:25378478 1332057 Rtcb RNA 2',3'-cyclic phosphate and 5'-OH ligase gene MP:0001926 female infertility IAGP N RGD:5509061 20230330 MGI PMID:36178098 1332057 Rtcb RNA 2',3'-cyclic phosphate and 5'-OH ligase gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20151008 MGI PMID:25378478 1332057 Rtcb RNA 2',3'-cyclic phosphate and 5'-OH ligase gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20151008 MGI PMID:25378478 1332057 Rtcb RNA 2',3'-cyclic phosphate and 5'-OH ligase gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20151008 MGI PMID:25378478 1332057 Rtcb RNA 2',3'-cyclic phosphate and 5'-OH ligase gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20230330 MGI PMID:36178098 1332057 Rtcb RNA 2',3'-cyclic phosphate and 5'-OH ligase gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20230330 MGI PMID:36178098 1332057 Rtcb RNA 2',3'-cyclic phosphate and 5'-OH ligase gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20230330 MGI PMID:36178098 1332058 Bod1 biorientation of chromosomes in cell division 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1332058 Bod1 biorientation of chromosomes in cell division 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1332058 Bod1 biorientation of chromosomes in cell division 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1332058 Bod1 biorientation of chromosomes in cell division 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1332058 Bod1 biorientation of chromosomes in cell division 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0001258 decreased body length IEA N RGD:5509061 20141003 MGI 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:22467576 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0001732 postnatal growth retardation IEA N RGD:5509061 20141003 MGI 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0002001 blindness IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0002698 abnormal sclera morphology IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:23839944 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20141003 MGI 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22467576 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22467576 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0004185 abnormal adipocyte glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:23839944 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0005098 abnormal optic choroid morphology IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23839944 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23839944 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0006237 abnormal choroid vasculature morphology IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:22467576 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20141003 MGI PMID:23839944 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:22467576 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:22467576 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0010192 abnormal retina melanin granule morphology IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:22467576 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0011232 abnormal vitamin A level IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0011233 abnormal vitamin A metabolism IAGP N RGD:5509061 20141030 MGI PMID:24391722 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0011233 abnormal vitamin A metabolism IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0011234 abnormal retinol level IAGP N RGD:5509061 20141003 MGI PMID:22467576 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0011996 abnormal retina inner nuclear layer thickness IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20150910 MGI PMID:24852372 1332061 Stra6 stimulated by retinoic acid gene 6 gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:24852372 1332062 Sv2b synaptic vesicle glycoprotein 2b gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11483953 1332062 Sv2b synaptic vesicle glycoprotein 2b gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23894296 1332062 Sv2b synaptic vesicle glycoprotein 2b gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10624962 1332062 Sv2b synaptic vesicle glycoprotein 2b gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11483953 1332062 Sv2b synaptic vesicle glycoprotein 2b gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10624962 1332062 Sv2b synaptic vesicle glycoprotein 2b gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:10624962 1332062 Sv2b synaptic vesicle glycoprotein 2b gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19381277 1332062 Sv2b synaptic vesicle glycoprotein 2b gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11483953 1332062 Sv2b synaptic vesicle glycoprotein 2b gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19381277 1332062 Sv2b synaptic vesicle glycoprotein 2b gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10624962 1332062 Sv2b synaptic vesicle glycoprotein 2b gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23894296 1332063 Sap130 Sin3A associated protein gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20200402 MGI 1332063 Sap130 Sin3A associated protein gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20170831 MGI PMID:28530678 1332063 Sap130 Sin3A associated protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21937600 1332063 Sap130 Sin3A associated protein gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20170831 MGI PMID:28530678 1332063 Sap130 Sin3A associated protein gene MP:0010446 heart left ventricle hypoplasia IAGP N RGD:5509061 20170824 MGI PMID:28530678 1332063 Sap130 Sin3A associated protein gene MP:0010463 aorta stenosis IAGP N RGD:5509061 20170824 MGI PMID:28530678 1332063 Sap130 Sin3A associated protein gene MP:0010541 aorta hypoplasia IAGP N RGD:5509061 20170831 MGI PMID:28530678 1332063 Sap130 Sin3A associated protein gene MP:0010580 decreased heart left ventricle size IAGP N RGD:5509061 20170831 MGI PMID:28530678 1332063 Sap130 Sin3A associated protein gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20170824 MGI PMID:28530678 1332063 Sap130 Sin3A associated protein gene MP:0011939 increased food intake IEA N RGD:5509061 20210128 MGI 1332063 Sap130 Sin3A associated protein gene MP:0031523 mitral valve hypoplasia IAGP N RGD:5509061 20240104 MGI PMID:28530678 1332064 Padi3 peptidyl arginine deiminase, type III gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20170119 MGI PMID:27866708 1332064 Padi3 peptidyl arginine deiminase, type III gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1332064 Padi3 peptidyl arginine deiminase, type III gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20170119 MGI PMID:27866708 1332064 Padi3 peptidyl arginine deiminase, type III gene MP:0002832 coarse hair IAGP N RGD:5509061 20170119 MGI PMID:27866708 1332064 Padi3 peptidyl arginine deiminase, type III gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20170119 MGI PMID:27866708 1332064 Padi3 peptidyl arginine deiminase, type III gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1332064 Padi3 peptidyl arginine deiminase, type III gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1332064 Padi3 peptidyl arginine deiminase, type III gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1332064 Padi3 peptidyl arginine deiminase, type III gene MP:0010179 rough coat IAGP N RGD:5509061 20170119 MGI PMID:27866708 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210805 MGI 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210805 MGI 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20210805 MGI 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210805 MGI 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0003488 decreased channel response intensity IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210805 MGI 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0009148 pancreas necrosis IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0014121 increased pancreatic islet cell apoptosis IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332067 Kcnh6 potassium voltage-gated channel, subfamily H (eag-related), member 6 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20200416 MGI PMID:30590050 1332070 Ybx2 Y box protein 2 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:15824319 1332070 Ybx2 Y box protein 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:15824319 1332070 Ybx2 Y box protein 2 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:15824319 1332070 Ybx2 Y box protein 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15824319 1332070 Ybx2 Y box protein 2 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15824319 1332070 Ybx2 Y box protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15824319 1332070 Ybx2 Y box protein 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15824319 1332070 Ybx2 Y box protein 2 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:15824319 1332070 Ybx2 Y box protein 2 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:15824319 1332070 Ybx2 Y box protein 2 gene MP:0003696 abnormal zona pellucida morphology IAGP N RGD:5509061 20141003 MGI PMID:15824319 1332070 Ybx2 Y box protein 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:15824319 1332070 Ybx2 Y box protein 2 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:15824319 1332070 Ybx2 Y box protein 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:15824319 1332070 Ybx2 Y box protein 2 gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220804 MGI PMID:15824319 1332071 Rbm48 RNA binding motif protein 48 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20230601 MGI 1332071 Rbm48 RNA binding motif protein 48 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1332071 Rbm48 RNA binding motif protein 48 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1332072 Ntan1 N-terminal Asn amidase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11689692 1332072 Ntan1 N-terminal Asn amidase gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10805755 1332072 Ntan1 N-terminal Asn amidase gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:10805755 1332072 Ntan1 N-terminal Asn amidase gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10805755 1332072 Ntan1 N-terminal Asn amidase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10805755 1332072 Ntan1 N-terminal Asn amidase gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10805755 1332072 Ntan1 N-terminal Asn amidase gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:10805755 1332072 Ntan1 N-terminal Asn amidase gene MP:0002798 abnormal active avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:10805755 1332072 Ntan1 N-terminal Asn amidase gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:10805755 1332072 Ntan1 N-terminal Asn amidase gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:10805755 1332072 Ntan1 N-terminal Asn amidase gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:10805755 1332072 Ntan1 N-terminal Asn amidase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:10805755 1332072 Ntan1 N-terminal Asn amidase gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:10805755 1332073 Pdap1 PDGFA associated protein 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20210708 MGI PMID:32609329 1332073 Pdap1 PDGFA associated protein 1 gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20210708 MGI PMID:32609329 1332073 Pdap1 PDGFA associated protein 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20210708 MGI PMID:32609329 1332073 Pdap1 PDGFA associated protein 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20210708 MGI PMID:32609329 1332073 Pdap1 PDGFA associated protein 1 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20210708 MGI PMID:32609329 1332073 Pdap1 PDGFA associated protein 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20210708 MGI PMID:32609329 1332073 Pdap1 PDGFA associated protein 1 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20210708 MGI PMID:32609329 1332074 Cnpy4 canopy FGF signaling regulator 4 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1332074 Cnpy4 canopy FGF signaling regulator 4 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20230601 MGI 1332074 Cnpy4 canopy FGF signaling regulator 4 gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 1332074 Cnpy4 canopy FGF signaling regulator 4 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1332074 Cnpy4 canopy FGF signaling regulator 4 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230601 MGI 1332074 Cnpy4 canopy FGF signaling regulator 4 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230601 MGI 1332076 Slain2 SLAIN motif family, member 2 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1332076 Slain2 SLAIN motif family, member 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 1332076 Slain2 SLAIN motif family, member 2 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20220811 MGI 1332076 Slain2 SLAIN motif family, member 2 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1332076 Slain2 SLAIN motif family, member 2 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1332076 Slain2 SLAIN motif family, member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1332077 Mlec malectin gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20150108 MGI 1332077 Mlec malectin gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1332077 Mlec malectin gene MP:0005477 increased circulating thyroxine level IEA N RGD:5509061 20210128 MGI 1332077 Mlec malectin gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 1332079 Cwh43 cell wall biogenesis 43 C-terminal homolog gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20230309 MGI PMID:33459505 1332079 Cwh43 cell wall biogenesis 43 C-terminal homolog gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1332079 Cwh43 cell wall biogenesis 43 C-terminal homolog gene MP:0001405 impaired coordination IAGP N RGD:5509061 20230309 MGI PMID:33459505 1332079 Cwh43 cell wall biogenesis 43 C-terminal homolog gene MP:0001406 abnormal gait IAGP N RGD:5509061 20230309 MGI PMID:33459505 1332079 Cwh43 cell wall biogenesis 43 C-terminal homolog gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20230309 MGI PMID:33459505 1332079 Cwh43 cell wall biogenesis 43 C-terminal homolog gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20230309 MGI PMID:33459505 1332079 Cwh43 cell wall biogenesis 43 C-terminal homolog gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20230309 MGI PMID:33459505 1332079 Cwh43 cell wall biogenesis 43 C-terminal homolog gene MP:0030966 decreased brain ependyma motile cilium number IAGP N RGD:5509061 20230309 MGI PMID:33459505 1332080 Egflam EGF-like, fibronectin type III and laminin G domains gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18641643 1332080 Egflam EGF-like, fibronectin type III and laminin G domains gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18641643 1332080 Egflam EGF-like, fibronectin type III and laminin G domains gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18641643 1332080 Egflam EGF-like, fibronectin type III and laminin G domains gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18641643 1332080 Egflam EGF-like, fibronectin type III and laminin G domains gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:18641643 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:17481393 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17481393 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150917 MGI PMID:24908665 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150917 MGI PMID:24908665 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:21903668 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160407 MGI PMID:26728762 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20160407 MGI PMID:26728762 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21903668 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220428 MGI 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17481393 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20160407 MGI PMID:26728762 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20141003 MGI PMID:17481393 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17481393 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21903668 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20150917 MGI PMID:24908665 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17481393 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20150917 MGI PMID:24908665 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0001577 anemia IAGP N RGD:5509061 20150917 MGI PMID:24908665 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:16484369 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21903668 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:17481393 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:17481393 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20150917 MGI PMID:24908665 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20160407 MGI PMID:26728762 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20160407 MGI PMID:26728762 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20150917 MGI PMID:24908665 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0002915 abnormal synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:21903668 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:17481393 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:21903668 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20160407 MGI PMID:26728762 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:17481393 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0006299 abnormal latent inhibition of conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17481393 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0006300 abnormal entorhinal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17481393 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:17481393 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21903668 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20150917 MGI PMID:24908665 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:21903668 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21903668 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20150917 MGI PMID:24908665 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20150917 MGI PMID:24908665 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:21903668 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20141003 MGI PMID:21903668 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0012347 low sweet preference IAGP N RGD:5509061 20150917 MGI PMID:24908665 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:17481393 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:21903668 1332081 Disc1 disrupted in schizophrenia 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:26728762 1332082 4930558K02Rik RIKEN cDNA 4930558K02 gene gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1332083 Actl9 actin-like 9 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20210429 MGI PMID:33626338 1332083 Actl9 actin-like 9 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210429 MGI PMID:33626338 1332083 Actl9 actin-like 9 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20210429 MGI PMID:33626338 1332083 Actl9 actin-like 9 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20210429 MGI PMID:33626338 1332083 Actl9 actin-like 9 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220303 MGI PMID:33626338 1332083 Actl9 actin-like 9 gene MP:0031355 abnormal proacrosomal vesicle fusion IAGP N RGD:5509061 20220303 MGI PMID:33626338 1332084 Slco1a5 solute carrier organic anion transporter family, member 1a5 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IEA N RGD:5509061 20111116 MGI 1332084 Slco1a5 solute carrier organic anion transporter family, member 1a5 gene MP:0005014 increased B cell number IEA N RGD:5509061 20111116 MGI 1332085 Ring1 ring finger protein 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11060235 1332085 Ring1 ring finger protein 1 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:11060235 1332085 Ring1 ring finger protein 1 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11060235 1332085 Ring1 ring finger protein 1 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:11060235 1332085 Ring1 ring finger protein 1 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:11060235 1332086 Khsrp KH-type splicing regulatory protein gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1332086 Khsrp KH-type splicing regulatory protein gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230601 MGI 1332086 Khsrp KH-type splicing regulatory protein gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:21690298 1332086 Khsrp KH-type splicing regulatory protein gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20230601 MGI 1332086 Khsrp KH-type splicing regulatory protein gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20231207 MGI 1332086 Khsrp KH-type splicing regulatory protein gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230601 MGI 1332086 Khsrp KH-type splicing regulatory protein gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:21690298 1332086 Khsrp KH-type splicing regulatory protein gene MP:0031025 decreased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:21690298 1332087 Pa2g4 proliferation-associated 2G4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19094237 1332087 Pa2g4 proliferation-associated 2G4 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:19094237 1332087 Pa2g4 proliferation-associated 2G4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19094237 1332087 Pa2g4 proliferation-associated 2G4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19094237 1332087 Pa2g4 proliferation-associated 2G4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19094237 1332087 Pa2g4 proliferation-associated 2G4 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1332087 Pa2g4 proliferation-associated 2G4 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:19094237 1332088 Sorbs3 sorbin and SH3 domain containing 3 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:20361963 1332088 Sorbs3 sorbin and SH3 domain containing 3 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:20361963 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220811 MGI PMID:35574006 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20201029 MGI PMID:31365862 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220811 MGI PMID:35574006 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16207763 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0002139 abnormal hepatobiliary system physiology IAGP N RGD:5509061 20141003 MGI PMID:12808103 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16207763 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:16207763 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:16611695 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0003095 abnormal cornea stroma development IAGP N RGD:5509061 20141003 MGI PMID:16207763 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0004054 abnormal periocular mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:16611695 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:16611695 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220811 MGI PMID:35574006 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0005195 abnormal posterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16611695 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20220811 MGI PMID:35574006 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0006162 thick eyelids IAGP N RGD:5509061 20141225 MGI PMID:16611695 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0008881 absent Harderian gland IAGP N RGD:5509061 20141003 MGI PMID:16207763 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20160324 MGI PMID:16207763 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0009742 increased cornea stroma thickness IAGP N RGD:5509061 20141225 MGI PMID:16611695 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0010706 ventral rotation of lens IAGP N RGD:5509061 20160324 MGI PMID:16207763 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0010707 decreased ventral retina size IAGP N RGD:5509061 20160324 MGI PMID:16207763 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0010708 absent iris stroma IAGP N RGD:5509061 20160324 MGI PMID:16207763 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0010710 absent sclera IAGP N RGD:5509061 20160324 MGI PMID:16207763 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:16207763 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:16611695 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16207763 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0011964 increased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:16611695 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0013744 abnormal conjunctival sac morphology IAGP N RGD:5509061 20160324 MGI PMID:16207763 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0030326 decreased periocular mesenchyme apoptosis IAGP N RGD:5509061 20171109 MGI PMID:16207763 1332089 Aldh1a1 aldehyde dehydrogenase family 1, subfamily A1 gene MP:0030326 decreased periocular mesenchyme apoptosis IAGP N RGD:5509061 20171109 MGI PMID:16611695 1332092 Cd200 CD200 molecule gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:11099416 1332092 Cd200 CD200 molecule gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20200310 MGI 1332092 Cd200 CD200 molecule gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:11099416 1332092 Cd200 CD200 molecule gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20200310 MGI PMID:11099416 1332092 Cd200 CD200 molecule gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20200310 MGI PMID:11099416 1332092 Cd200 CD200 molecule gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:11099416 1332092 Cd200 CD200 molecule gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20200310 MGI PMID:11099416 1332092 Cd200 CD200 molecule gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20200310 MGI PMID:11099416 1332092 Cd200 CD200 molecule gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20200310 MGI PMID:11099416 1332092 Cd200 CD200 molecule gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200310 MGI PMID:11099416 1332092 Cd200 CD200 molecule gene MP:0004821 increased susceptibility to experimental autoimmune uveoretinitis IAGP N RGD:5509061 20200310 MGI PMID:12414514 1332092 Cd200 CD200 molecule gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20200310 MGI PMID:11099416 1332092 Cd200 CD200 molecule gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20200310 MGI PMID:12414514 1332092 Cd200 CD200 molecule gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:12414514 1332092 Cd200 CD200 molecule gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20200310 MGI PMID:11099416 1332092 Cd200 CD200 molecule gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20200310 MGI PMID:15611236 1332092 Cd200 CD200 molecule gene MP:0010052 increased grip strength IEA N RGD:5509061 20200310 MGI 1332095 Vps13d vacuolar protein sorting 13D gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20111116 MGI 1332095 Vps13d vacuolar protein sorting 13D gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200402 MGI 1332095 Vps13d vacuolar protein sorting 13D gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1332096 Crygf crystallin, gamma F gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:3352637 1332097 Secisbp2 SECIS binding protein 2 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1332097 Secisbp2 SECIS binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190801 MGI PMID:29029094 1332097 Secisbp2 SECIS binding protein 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1332097 Secisbp2 SECIS binding protein 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:24274065 1332097 Secisbp2 SECIS binding protein 2 gene MP:0001775 abnormal selenium level IAGP N RGD:5509061 20141003 MGI PMID:24274065 1332097 Secisbp2 SECIS binding protein 2 gene MP:0001924 infertility IAGP N RGD:5509061 20190801 MGI PMID:29029094 1332097 Secisbp2 SECIS binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20190801 MGI PMID:29029094 1332097 Secisbp2 SECIS binding protein 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24274065 1332097 Secisbp2 SECIS binding protein 2 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20190801 MGI PMID:29029094 1332097 Secisbp2 SECIS binding protein 2 gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20190801 MGI PMID:29029094 1332097 Secisbp2 SECIS binding protein 2 gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20190801 MGI PMID:29029094 1332097 Secisbp2 SECIS binding protein 2 gene MP:0005473 decreased triiodothyronine level IAGP N RGD:5509061 20190801 MGI PMID:29029094 1332097 Secisbp2 SECIS binding protein 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20190801 MGI PMID:29029094 1332097 Secisbp2 SECIS binding protein 2 gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20190801 MGI PMID:29029094 1332097 Secisbp2 SECIS binding protein 2 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20160804 MGI 1332097 Secisbp2 SECIS binding protein 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20190801 MGI PMID:29029094 1332097 Secisbp2 SECIS binding protein 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24274065 1332097 Secisbp2 SECIS binding protein 2 gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24274065 1332097 Secisbp2 SECIS binding protein 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24274065 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200806 MGI PMID:31285585 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20200806 MGI PMID:31285585 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20200806 MGI PMID:31285585 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20200806 MGI PMID:31285585 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20200806 MGI PMID:31285585 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0003288 intestinal edema IAGP N RGD:5509061 20200806 MGI PMID:31285585 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0003332 liver abscess IAGP N RGD:5509061 20200806 MGI PMID:31285585 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20201022 MGI 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20200806 MGI PMID:31285585 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20200806 MGI PMID:31285585 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20200806 MGI PMID:31285585 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200806 MGI PMID:31285585 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20200806 MGI PMID:31285585 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201022 MGI 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0013793 abnormal large intestine goblet cell morphology IAGP N RGD:5509061 20200806 MGI PMID:31285585 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20200806 MGI PMID:31285585 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0031113 pulmonary parenchymal consolidation IAGP N RGD:5509061 20200806 MGI PMID:31285585 1332100 Cyrib CYFIP related Rac1 interactor B gene MP:0031220 increased circulating CXCL10 level IAGP N RGD:5509061 20210204 MGI PMID:31285585 1332101 Gsdmd gasdermin D gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18693275 1332101 Gsdmd gasdermin D gene MP:0005036 diarrhea IAGP N RGD:5509061 20180111 MGI PMID:28636595 1332101 Gsdmd gasdermin D gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20160630 MGI PMID:26375003 1332101 Gsdmd gasdermin D gene MP:0011073 abnormal macrophage apoptosis IAGP N RGD:5509061 20160630 MGI PMID:26375003 1332101 Gsdmd gasdermin D gene MP:0020186 abnormal susceptibility to bacterial infection IEA N RGD:5509061 20180920 MGI 1332101 Gsdmd gasdermin D gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:28636595 1332106 Ndnf neuron-derived neurotrophic factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26727548 1332106 Ndnf neuron-derived neurotrophic factor gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20220421 MGI PMID:35051783 1332106 Ndnf neuron-derived neurotrophic factor gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20220421 MGI PMID:35051783 1332106 Ndnf neuron-derived neurotrophic factor gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20220421 MGI PMID:35051783 1332107 Gsc goosecoid homeobox gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0000098 abnormal vomer bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0000098 abnormal vomer bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0000100 abnormal ethmoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10512191 1332107 Gsc goosecoid homeobox gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:17127040 1332107 Gsc goosecoid homeobox gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:17127040 1332107 Gsc goosecoid homeobox gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17127040 1332107 Gsc goosecoid homeobox gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0002234 abnormal pharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0002238 abnormal nasal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0003110 absent malleus processus brevis IAGP N RGD:5509061 20141003 MGI PMID:10512191 1332107 Gsc goosecoid homeobox gene MP:0003110 absent malleus processus brevis IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0004234 abnormal masticatory muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0004450 presphenoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0004456 small pterygoid bone IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0004459 small alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0004475 palatine bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0004554 small pharynx IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20171102 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0004627 abnormal trochanter morphology IAGP N RGD:5509061 20141003 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0004689 small ischium IAGP N RGD:5509061 20181011 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0004873 absent turbinates IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:10512191 1332107 Gsc goosecoid homeobox gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0006018 abnormal tympanic membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0006019 absent tympanic membrane IAGP N RGD:5509061 20141003 MGI PMID:10512191 1332107 Gsc goosecoid homeobox gene MP:0006019 absent tympanic membrane IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:10512191 1332107 Gsc goosecoid homeobox gene MP:0006033 abnormal external auditory canal morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0006294 absent optic vesicle IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0006338 abnormal second pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0008376 small malleus manubrium IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0008376 small malleus manubrium IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0008378 small malleus processus brevis IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0009575 abnormal pubic symphysis morphology IAGP N RGD:5509061 20181011 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0009707 absent external auditory canal IAGP N RGD:5509061 20141003 MGI PMID:10512191 1332107 Gsc goosecoid homeobox gene MP:0009707 absent external auditory canal IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20171123 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0010355 abnormal first pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0010549 absent dorsal mesocardium IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0012069 abnormal horizontal basal cell of olfactory epithelium morphology IAGP N RGD:5509061 20171026 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:17127040 1332107 Gsc goosecoid homeobox gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0012263 decreased hindbrain size IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:9226455 1332107 Gsc goosecoid homeobox gene MP:0030059 absent ethmoturbinates IAGP N RGD:5509061 20170921 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0030154 abnormal tympanic cavity morphology IAGP N RGD:5509061 20171005 MGI PMID:10512191 1332107 Gsc goosecoid homeobox gene MP:0030187 abnormal epitympanic recess morphology IAGP N RGD:5509061 20171012 MGI PMID:10512191 1332107 Gsc goosecoid homeobox gene MP:0030208 abnormal intrinsic tongue muscle morphology IAGP N RGD:5509061 20171026 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0030209 abnormal extrinsic tongue muscle morphology IAGP N RGD:5509061 20171019 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0030210 abnormal genioglossus muscle morphology IAGP N RGD:5509061 20171019 MGI PMID:7555726 1332107 Gsc goosecoid homeobox gene MP:0030266 small vomer bone IAGP N RGD:5509061 20171026 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0030266 small vomer bone IAGP N RGD:5509061 20171026 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0030283 small mandibular coronoid process IAGP N RGD:5509061 20171102 MGI PMID:7555718 1332107 Gsc goosecoid homeobox gene MP:0030305 small cribriform plate IAGP N RGD:5509061 20171109 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0030788 abnormal femur head morphology IAGP N RGD:5509061 20181011 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0030816 abnormal shoulder joint morphology IAGP N RGD:5509061 20181018 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0030828 abnormal obturator foramen morphology IAGP N RGD:5509061 20181018 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0030829 abnormal hip joint morphology IAGP N RGD:5509061 20181018 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0030830 abnormal acetabulum morphology IAGP N RGD:5509061 20181018 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0030831 abnormal glenoid fossa morphology IAGP N RGD:5509061 20181018 MGI PMID:9533949 1332107 Gsc goosecoid homeobox gene MP:0030832 abnormal scapular coracoid process morphology IAGP N RGD:5509061 20181018 MGI PMID:9533949 1332108 Cyp2a12 cytochrome P450, family 2, subfamily a, polypeptide 12 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20240613 MGI PMID:31645370 1332108 Cyp2a12 cytochrome P450, family 2, subfamily a, polypeptide 12 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20240613 MGI PMID:31645370 1332108 Cyp2a12 cytochrome P450, family 2, subfamily a, polypeptide 12 gene MP:0002083 premature death IAGP N RGD:5509061 20240613 MGI PMID:31645370 1332108 Cyp2a12 cytochrome P450, family 2, subfamily a, polypeptide 12 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20240613 MGI PMID:31645370 1332108 Cyp2a12 cytochrome P450, family 2, subfamily a, polypeptide 12 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20240613 MGI PMID:31645370 1332108 Cyp2a12 cytochrome P450, family 2, subfamily a, polypeptide 12 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20240613 MGI PMID:31645370 1332108 Cyp2a12 cytochrome P450, family 2, subfamily a, polypeptide 12 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20240613 MGI PMID:31645370 1332108 Cyp2a12 cytochrome P450, family 2, subfamily a, polypeptide 12 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20240613 MGI PMID:31645370 1332108 Cyp2a12 cytochrome P450, family 2, subfamily a, polypeptide 12 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20240613 MGI PMID:31645370 1332108 Cyp2a12 cytochrome P450, family 2, subfamily a, polypeptide 12 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20240613 MGI PMID:31645370 1332108 Cyp2a12 cytochrome P450, family 2, subfamily a, polypeptide 12 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20240613 MGI PMID:31645370 1332108 Cyp2a12 cytochrome P450, family 2, subfamily a, polypeptide 12 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20240613 MGI PMID:31645370 1332108 Cyp2a12 cytochrome P450, family 2, subfamily a, polypeptide 12 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20240613 MGI PMID:31645370 1332108 Cyp2a12 cytochrome P450, family 2, subfamily a, polypeptide 12 gene MP:0012338 decreased bile salt level IAGP N RGD:5509061 20240613 MGI PMID:31645370 1332108 Cyp2a12 cytochrome P450, family 2, subfamily a, polypeptide 12 gene MP:0014479 decreased feces bile salt level IAGP N RGD:5509061 20240704 MGI PMID:31645370 1332109 Cpsf7 cleavage and polyadenylation specific factor 7 gene MP:0001304 cataract IEA N RGD:5509061 20190502 MGI 1332109 Cpsf7 cleavage and polyadenylation specific factor 7 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1332110 Aacs acetoacetyl-CoA synthetase gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1332115 Nmur2 neuromedin U receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:19324999 1332115 Nmur2 neuromedin U receptor 2 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20200310 MGI PMID:17030627 1332115 Nmur2 neuromedin U receptor 2 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20200310 MGI PMID:17030627 1332115 Nmur2 neuromedin U receptor 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:17030627 1332115 Nmur2 neuromedin U receptor 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:17379411 1332115 Nmur2 neuromedin U receptor 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20200310 MGI PMID:19324999 1332115 Nmur2 neuromedin U receptor 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20200310 MGI PMID:19584200 1332115 Nmur2 neuromedin U receptor 2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20200310 MGI PMID:19324999 1332115 Nmur2 neuromedin U receptor 2 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20200310 MGI PMID:17030627 1332115 Nmur2 neuromedin U receptor 2 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20200310 MGI PMID:19584200 1332115 Nmur2 neuromedin U receptor 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:19324999 1332115 Nmur2 neuromedin U receptor 2 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:19584200 1332115 Nmur2 neuromedin U receptor 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:19324999 1332115 Nmur2 neuromedin U receptor 2 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:19324999 1332115 Nmur2 neuromedin U receptor 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200310 MGI PMID:19324999 1332115 Nmur2 neuromedin U receptor 2 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:17379411 1332115 Nmur2 neuromedin U receptor 2 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:19584200 1332115 Nmur2 neuromedin U receptor 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:19324999 1332115 Nmur2 neuromedin U receptor 2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20200310 MGI PMID:19324999 1332115 Nmur2 neuromedin U receptor 2 gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20200310 MGI PMID:17030627 1332116 Pyroxd1 pyridine nucleotide-disulphide oxidoreductase domain 1 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20161201 MGI 1332116 Pyroxd1 pyridine nucleotide-disulphide oxidoreductase domain 1 gene MP:0000745 tremors IEA N RGD:5509061 20190502 MGI 1332116 Pyroxd1 pyridine nucleotide-disulphide oxidoreductase domain 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332116 Pyroxd1 pyridine nucleotide-disulphide oxidoreductase domain 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1332117 Sema3d sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D gene MP:0002726 abnormal pulmonary vein morphology IAGP N RGD:5509061 20141003 MGI PMID:23685842 1332117 Sema3d sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:23685842 1332117 Sema3d sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D gene MP:0008727 increased heart right atrium size IAGP N RGD:5509061 20141003 MGI PMID:23685842 1332117 Sema3d sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20141003 MGI PMID:23685842 1332117 Sema3d sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:23685842 1332117 Sema3d sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332117 Sema3d sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D gene MP:0031129 left-to-right shunt IAGP N RGD:5509061 20201015 MGI PMID:23685842 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:19056871 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:19056871 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:19056871 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:19056871 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0010110 abnormal renal phosphate reabsorption IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:19056871 1332118 Slc34a3 solute carrier family 34 (sodium phosphate), member 3 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:19570882 1332119 Siae sialic acid acetylesterase gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0008169 increased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20170622 MGI PMID:27210752 1332119 Siae sialic acid acetylesterase gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:19103880 1332119 Siae sialic acid acetylesterase gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20170622 MGI PMID:27210752 1332119 Siae sialic acid acetylesterase gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:19103880 1332120 Cgref1 cell growth regulator with EF hand domain 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220519 MGI 1332120 Cgref1 cell growth regulator with EF hand domain 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201231 MGI 1332120 Cgref1 cell growth regulator with EF hand domain 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200402 MGI 1332120 Cgref1 cell growth regulator with EF hand domain 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 1332120 Cgref1 cell growth regulator with EF hand domain 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1332121 Emc3 ER membrane protein complex subunit 3 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20191128 MGI PMID:31263175 1332121 Emc3 ER membrane protein complex subunit 3 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20210520 MGI 1332121 Emc3 ER membrane protein complex subunit 3 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20191128 MGI PMID:31263175 1332121 Emc3 ER membrane protein complex subunit 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1332121 Emc3 ER membrane protein complex subunit 3 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20191128 MGI PMID:31263175 1332121 Emc3 ER membrane protein complex subunit 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210520 MGI 1332121 Emc3 ER membrane protein complex subunit 3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 1332121 Emc3 ER membrane protein complex subunit 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332122 Emc1 ER membrane protein complex subunit 1 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20240328 MGI PMID:37098815 1332122 Emc1 ER membrane protein complex subunit 1 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20240328 MGI PMID:37098815 1332122 Emc1 ER membrane protein complex subunit 1 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20240328 MGI PMID:37098815 1332122 Emc1 ER membrane protein complex subunit 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20240328 MGI PMID:37098815 1332122 Emc1 ER membrane protein complex subunit 1 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20240328 MGI PMID:37098815 1332122 Emc1 ER membrane protein complex subunit 1 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20240328 MGI PMID:37098815 1332122 Emc1 ER membrane protein complex subunit 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20240328 MGI PMID:37098815 1332122 Emc1 ER membrane protein complex subunit 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20240328 MGI PMID:37098815 1332122 Emc1 ER membrane protein complex subunit 1 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20240328 MGI PMID:37098815 1332122 Emc1 ER membrane protein complex subunit 1 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20240328 MGI PMID:37098815 1332122 Emc1 ER membrane protein complex subunit 1 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20240328 MGI PMID:37098815 1332122 Emc1 ER membrane protein complex subunit 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20240328 MGI PMID:37098815 1332122 Emc1 ER membrane protein complex subunit 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20240328 MGI PMID:37098815 1332122 Emc1 ER membrane protein complex subunit 1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20240328 MGI PMID:37098815 1332123 Rasal3 RAS protein activator like 3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20160707 MGI PMID:25652366 1332123 Rasal3 RAS protein activator like 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1332123 Rasal3 RAS protein activator like 3 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1332123 Rasal3 RAS protein activator like 3 gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 1332123 Rasal3 RAS protein activator like 3 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20160707 MGI PMID:25652366 1332123 Rasal3 RAS protein activator like 3 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1332123 Rasal3 RAS protein activator like 3 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1332123 Rasal3 RAS protein activator like 3 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20160707 MGI PMID:25652366 1332123 Rasal3 RAS protein activator like 3 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1332123 Rasal3 RAS protein activator like 3 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20181227 MGI 1332123 Rasal3 RAS protein activator like 3 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20160707 MGI PMID:25652366 1332123 Rasal3 RAS protein activator like 3 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20160707 MGI PMID:25652366 1332123 Rasal3 RAS protein activator like 3 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20160707 MGI PMID:25652366 1332123 Rasal3 RAS protein activator like 3 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20160707 MGI PMID:25652366 1332123 Rasal3 RAS protein activator like 3 gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20160707 MGI PMID:25652366 1332123 Rasal3 RAS protein activator like 3 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20160707 MGI PMID:25652366 1332123 Rasal3 RAS protein activator like 3 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20211021 MGI 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18602915 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12740569 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12740569 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:12740569 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12740569 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18602915 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20160421 MGI PMID:23413146 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0003337 exocrine pancreas hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12740569 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20141003 MGI PMID:12740569 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20160421 MGI PMID:23413146 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12740569 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:12740569 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12740569 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20201022 MGI 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:12740569 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12740569 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20160421 MGI PMID:23413146 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20160421 MGI PMID:23413146 1332124 Serpinf1 serine (or cysteine) peptidase inhibitor, clade F, member 1 gene MP:0010929 increased osteoid thickness IAGP N RGD:5509061 20160421 MGI PMID:23413146 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20240523 MGI 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20231207 MGI 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0002980 abnormal postural reflex IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0003173 decreased lysosomal enzyme secretion IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0004867 decreased platelet calcium level IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:12445206 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0005077 abnormal melanogenesis IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0005098 abnormal optic choroid morphology IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0005100 abnormal choroid pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20240523 MGI 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20141003 MGI PMID:12576321 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170720 MGI PMID:11110696 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0030915 abnormal melanosome maturation IAGP N RGD:5509061 20181227 MGI PMID:12445206 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0030916 abnormal melanosome size IAGP N RGD:5509061 20181227 MGI PMID:12445206 1332125 Bloc1s4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino gene MP:0030918 small melanosome IAGP N RGD:5509061 20181227 MGI PMID:12445206 1332126 Uevld UEV and lactate/malate dehyrogenase domains gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210520 MGI 1332127 Flywch2 FLYWCH family member 2 gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20211021 MGI 1332128 Eri2 exoribonuclease 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1332129 Igsf1 immunoglobulin superfamily, member 1 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20161222 MGI PMID:23143598 1332129 Igsf1 immunoglobulin superfamily, member 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20161222 MGI PMID:23143598 1332129 Igsf1 immunoglobulin superfamily, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12832474 1332129 Igsf1 immunoglobulin superfamily, member 1 gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20161222 MGI PMID:23143598 1332129 Igsf1 immunoglobulin superfamily, member 1 gene MP:0005119 decreased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20161222 MGI PMID:23143598 1332129 Igsf1 immunoglobulin superfamily, member 1 gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20161222 MGI PMID:23143598 1332129 Igsf1 immunoglobulin superfamily, member 1 gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20161222 MGI PMID:23143598 1332131 Mast1 microtubule associated serine/threonine kinase 1 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20190926 MGI PMID:30449657 1332131 Mast1 microtubule associated serine/threonine kinase 1 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20190926 MGI PMID:30449657 1332131 Mast1 microtubule associated serine/threonine kinase 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20190926 MGI PMID:30449657 1332131 Mast1 microtubule associated serine/threonine kinase 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20190926 MGI PMID:30449657 1332131 Mast1 microtubule associated serine/threonine kinase 1 gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20190926 MGI PMID:30449657 1332131 Mast1 microtubule associated serine/threonine kinase 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20190926 MGI PMID:30449657 1332131 Mast1 microtubule associated serine/threonine kinase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20190926 MGI PMID:30449657 1332131 Mast1 microtubule associated serine/threonine kinase 1 gene MP:0012443 increased corpus callosum size IAGP N RGD:5509061 20190926 MGI PMID:30449657 1332133 Ntaq1 N-terminal glutamine amidase 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1332133 Ntaq1 N-terminal glutamine amidase 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1332133 Ntaq1 N-terminal glutamine amidase 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1332133 Ntaq1 N-terminal glutamine amidase 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:23159736 1332133 Ntaq1 N-terminal glutamine amidase 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 1332133 Ntaq1 N-terminal glutamine amidase 1 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20230601 MGI 1332133 Ntaq1 N-terminal glutamine amidase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 1332134 Pias3 protein inhibitor of activated STAT 3 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20171214 MGI PMID:28495965 1332134 Pias3 protein inhibitor of activated STAT 3 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20171214 MGI PMID:28495965 1332134 Pias3 protein inhibitor of activated STAT 3 gene MP:0031273 decreased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20240718 MGI PMID:37008329 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0004131 abnormal motile primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0008926 abnormal anterior definitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0011998 decreased embryonic cilium length IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:15371312 1332135 Dync2li1 dynein cytoplasmic 2 light intermediate chain 1 gene MP:0030538 abnormal notochordal plate morphology IAGP N RGD:5509061 20180201 MGI PMID:15371312 1332138 Cabs1 calcium binding protein, spermatid specific 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210506 MGI PMID:33440775 1332138 Cabs1 calcium binding protein, spermatid specific 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210506 MGI PMID:33440775 1332138 Cabs1 calcium binding protein, spermatid specific 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201022 MGI PMID:32588039 1332138 Cabs1 calcium binding protein, spermatid specific 1 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20210506 MGI PMID:33440775 1332138 Cabs1 calcium binding protein, spermatid specific 1 gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20210506 MGI PMID:33440775 1332138 Cabs1 calcium binding protein, spermatid specific 1 gene MP:0009835 absent sperm annulus IAGP N RGD:5509061 20210506 MGI PMID:33440775 1332140 Caml calcium modulating ligand gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16111633 1332140 Caml calcium modulating ligand gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:16111633 1332140 Caml calcium modulating ligand gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:16111633 1332140 Caml calcium modulating ligand gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16111633 1332140 Caml calcium modulating ligand gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16111633 1332140 Caml calcium modulating ligand gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12919676 1332143 Trpv2 transient receptor potential cation channel, subfamily V, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20118928 1332143 Trpv2 transient receptor potential cation channel, subfamily V, member 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:20118928 1332143 Trpv2 transient receptor potential cation channel, subfamily V, member 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20118928 1332143 Trpv2 transient receptor potential cation channel, subfamily V, member 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20118928 1332143 Trpv2 transient receptor potential cation channel, subfamily V, member 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20118928 1332145 Commd10 COMM domain containing 10 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20180201 MGI PMID:26001274 1332145 Commd10 COMM domain containing 10 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180201 MGI PMID:26847029 1332145 Commd10 COMM domain containing 10 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20230420 MGI PMID:36062803 1332145 Commd10 COMM domain containing 10 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:21339326 1332145 Commd10 COMM domain containing 10 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:23795291 1332145 Commd10 COMM domain containing 10 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20200820 MGI PMID:32704094 1332145 Commd10 COMM domain containing 10 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20180201 MGI PMID:26001274 1332145 Commd10 COMM domain containing 10 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20180201 MGI PMID:21339326 1332145 Commd10 COMM domain containing 10 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20180201 MGI PMID:23795291 1332145 Commd10 COMM domain containing 10 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20190103 MGI PMID:30423293 1332145 Commd10 COMM domain containing 10 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200820 MGI PMID:32704094 1332145 Commd10 COMM domain containing 10 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0000603 pale liver IAGP N RGD:5509061 20200820 MGI PMID:32704094 1332145 Commd10 COMM domain containing 10 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20220616 MGI PMID:29127143 1332145 Commd10 COMM domain containing 10 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20180201 MGI PMID:26001274 1332145 Commd10 COMM domain containing 10 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20230420 MGI PMID:36062803 1332145 Commd10 COMM domain containing 10 gene MP:0000692 small spleen IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0000692 small spleen IAGP N RGD:5509061 20210415 MGI PMID:29967452 1332145 Commd10 COMM domain containing 10 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0000706 small thymus IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0000706 small thymus IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20180201 MGI PMID:21258009 1332145 Commd10 COMM domain containing 10 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:23795291 1332145 Commd10 COMM domain containing 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20190530 MGI PMID:30237863 1332145 Commd10 COMM domain containing 10 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0001577 anemia IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0001577 anemia IAGP N RGD:5509061 20180201 MGI PMID:22659386 1332145 Commd10 COMM domain containing 10 gene MP:0001577 anemia IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0001577 anemia IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20180201 MGI PMID:22186994 1332145 Commd10 COMM domain containing 10 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20200820 MGI PMID:32704094 1332145 Commd10 COMM domain containing 10 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1332145 Commd10 COMM domain containing 10 gene MP:0001785 edema IAGP N RGD:5509061 20180201 MGI PMID:22186994 1332145 Commd10 COMM domain containing 10 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20180201 MGI PMID:24030045 1332145 Commd10 COMM domain containing 10 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:21258009 1332145 Commd10 COMM domain containing 10 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20180201 MGI PMID:21258009 1332145 Commd10 COMM domain containing 10 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20220616 MGI PMID:29127143 1332145 Commd10 COMM domain containing 10 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20220616 MGI PMID:29127143 1332145 Commd10 COMM domain containing 10 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20220616 MGI PMID:29127143 1332145 Commd10 COMM domain containing 10 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20200820 MGI PMID:32704094 1332145 Commd10 COMM domain containing 10 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20180201 MGI PMID:22186994 1332145 Commd10 COMM domain containing 10 gene MP:0001993 abnormal blinking IAGP N RGD:5509061 20180201 MGI PMID:28114589 1332145 Commd10 COMM domain containing 10 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20190530 MGI PMID:30237863 1332145 Commd10 COMM domain containing 10 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20180201 MGI PMID:21148330 1332145 Commd10 COMM domain containing 10 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0002083 premature death IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0002083 premature death IAGP N RGD:5509061 20220616 MGI PMID:29127143 1332145 Commd10 COMM domain containing 10 gene MP:0002083 premature death IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20180201 MGI PMID:23795291 1332145 Commd10 COMM domain containing 10 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:23293022 1332145 Commd10 COMM domain containing 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:24894949 1332145 Commd10 COMM domain containing 10 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20200206 MGI PMID:31434684 1332145 Commd10 COMM domain containing 10 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20180201 MGI PMID:22659386 1332145 Commd10 COMM domain containing 10 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20180201 MGI PMID:22659386 1332145 Commd10 COMM domain containing 10 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20190103 MGI PMID:30423293 1332145 Commd10 COMM domain containing 10 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20180201 MGI PMID:18676810 1332145 Commd10 COMM domain containing 10 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20200206 MGI PMID:31434684 1332145 Commd10 COMM domain containing 10 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180201 MGI PMID:24048899 1332145 Commd10 COMM domain containing 10 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200206 MGI PMID:31434684 1332145 Commd10 COMM domain containing 10 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20190530 MGI PMID:30237863 1332145 Commd10 COMM domain containing 10 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20180201 MGI PMID:25129145 1332145 Commd10 COMM domain containing 10 gene MP:0002491 decreased IgD level IAGP N RGD:5509061 20180201 MGI PMID:25057009 1332145 Commd10 COMM domain containing 10 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20180201 MGI PMID:25057009 1332145 Commd10 COMM domain containing 10 gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20200206 MGI PMID:31434684 1332145 Commd10 COMM domain containing 10 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20180201 MGI PMID:26001274 1332145 Commd10 COMM domain containing 10 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20180201 MGI PMID:24121508 1332145 Commd10 COMM domain containing 10 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0002812 spherocytosis IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0002872 polycythemia IAGP N RGD:5509061 20180201 MGI PMID:24121508 1332145 Commd10 COMM domain containing 10 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:23795291 1332145 Commd10 COMM domain containing 10 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:26001274 1332145 Commd10 COMM domain containing 10 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200820 MGI PMID:32704094 1332145 Commd10 COMM domain containing 10 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20220616 MGI PMID:29127143 1332145 Commd10 COMM domain containing 10 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20180201 MGI PMID:24121508 1332145 Commd10 COMM domain containing 10 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20180201 MGI PMID:23795291 1332145 Commd10 COMM domain containing 10 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20180201 MGI PMID:24030045 1332145 Commd10 COMM domain containing 10 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20180201 MGI PMID:20639863 1332145 Commd10 COMM domain containing 10 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0003717 pallor IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20220616 MGI PMID:29127143 1332145 Commd10 COMM domain containing 10 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20200820 MGI PMID:32704094 1332145 Commd10 COMM domain containing 10 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20230420 MGI PMID:36062803 1332145 Commd10 COMM domain containing 10 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20200206 MGI PMID:31434684 1332145 Commd10 COMM domain containing 10 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20180201 MGI PMID:26001274 1332145 Commd10 COMM domain containing 10 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20220616 MGI PMID:29127143 1332145 Commd10 COMM domain containing 10 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20180201 MGI PMID:21339326 1332145 Commd10 COMM domain containing 10 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20180201 MGI PMID:22763442 1332145 Commd10 COMM domain containing 10 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1332145 Commd10 COMM domain containing 10 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20180201 MGI PMID:21339326 1332145 Commd10 COMM domain containing 10 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20180201 MGI PMID:23795291 1332145 Commd10 COMM domain containing 10 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20180201 MGI PMID:24591644 1332145 Commd10 COMM domain containing 10 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20190103 MGI PMID:30423293 1332145 Commd10 COMM domain containing 10 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20180201 MGI PMID:18676810 1332145 Commd10 COMM domain containing 10 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20230330 MGI PMID:35987460 1332145 Commd10 COMM domain containing 10 gene MP:0004969 pale kidney IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0004975 absent regulatory T cells IAGP N RGD:5509061 20220616 MGI PMID:29127143 1332145 Commd10 COMM domain containing 10 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20230420 MGI PMID:36062803 1332145 Commd10 COMM domain containing 10 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20230420 MGI PMID:36062803 1332145 Commd10 COMM domain containing 10 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20230330 MGI PMID:35987460 1332145 Commd10 COMM domain containing 10 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200206 MGI PMID:31434684 1332145 Commd10 COMM domain containing 10 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180201 MGI PMID:18676810 1332145 Commd10 COMM domain containing 10 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180201 MGI PMID:21339326 1332145 Commd10 COMM domain containing 10 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180201 MGI PMID:24591644 1332145 Commd10 COMM domain containing 10 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200820 MGI PMID:32704094 1332145 Commd10 COMM domain containing 10 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20180201 MGI PMID:21258009 1332145 Commd10 COMM domain containing 10 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20180201 MGI PMID:21339326 1332145 Commd10 COMM domain containing 10 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20190530 MGI PMID:30237863 1332145 Commd10 COMM domain containing 10 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1332145 Commd10 COMM domain containing 10 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20180201 MGI PMID:25129145 1332145 Commd10 COMM domain containing 10 gene MP:0005068 abnormal NK cell morphology IAGP N RGD:5509061 20210415 MGI PMID:29967452 1332145 Commd10 COMM domain containing 10 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20210422 MGI PMID:26851218 1332145 Commd10 COMM domain containing 10 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20180201 MGI PMID:21258009 1332145 Commd10 COMM domain containing 10 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20180201 MGI PMID:18676810 1332145 Commd10 COMM domain containing 10 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20220616 MGI PMID:29127143 1332145 Commd10 COMM domain containing 10 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20220616 MGI PMID:29127143 1332145 Commd10 COMM domain containing 10 gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20180201 MGI PMID:25129145 1332145 Commd10 COMM domain containing 10 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0005426 tachypnea IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0005462 abnormal mast cell differentiation IAGP N RGD:5509061 20180201 MGI PMID:24204913 1332145 Commd10 COMM domain containing 10 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20180201 MGI PMID:26001274 1332145 Commd10 COMM domain containing 10 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20180201 MGI PMID:24121508 1332145 Commd10 COMM domain containing 10 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20180201 MGI PMID:27939640 1332145 Commd10 COMM domain containing 10 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20180201 MGI PMID:26001274 1332145 Commd10 COMM domain containing 10 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20180201 MGI PMID:22763442 1332145 Commd10 COMM domain containing 10 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20180201 MGI PMID:21258009 1332145 Commd10 COMM domain containing 10 gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20180201 MGI PMID:21339326 1332145 Commd10 COMM domain containing 10 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20200820 MGI PMID:32704094 1332145 Commd10 COMM domain containing 10 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20210415 MGI PMID:29967452 1332145 Commd10 COMM domain containing 10 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20210422 MGI PMID:26851218 1332145 Commd10 COMM domain containing 10 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20210422 MGI PMID:26851218 1332145 Commd10 COMM domain containing 10 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190530 MGI PMID:30237863 1332145 Commd10 COMM domain containing 10 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200820 MGI PMID:32704094 1332145 Commd10 COMM domain containing 10 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20180201 MGI PMID:24591644 1332145 Commd10 COMM domain containing 10 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20200820 MGI PMID:32704094 1332145 Commd10 COMM domain containing 10 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20230413 MGI PMID:35732734 1332145 Commd10 COMM domain containing 10 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20200206 MGI PMID:31434684 1332145 Commd10 COMM domain containing 10 gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20180201 MGI PMID:18538592 1332145 Commd10 COMM domain containing 10 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20180201 MGI PMID:18371367 1332145 Commd10 COMM domain containing 10 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:21339326 1332145 Commd10 COMM domain containing 10 gene MP:0008247 abnormal mononuclear cell morphology IAGP N RGD:5509061 20200820 MGI PMID:32704094 1332145 Commd10 COMM domain containing 10 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20180201 MGI PMID:21339326 1332145 Commd10 COMM domain containing 10 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20180201 MGI PMID:22763442 1332145 Commd10 COMM domain containing 10 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20180201 MGI PMID:21258009 1332145 Commd10 COMM domain containing 10 gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20180201 MGI PMID:24030045 1332145 Commd10 COMM domain containing 10 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20230420 MGI PMID:36062803 1332145 Commd10 COMM domain containing 10 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20200206 MGI PMID:31434684 1332145 Commd10 COMM domain containing 10 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20200206 MGI PMID:31434684 1332145 Commd10 COMM domain containing 10 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20180201 MGI PMID:24591644 1332145 Commd10 COMM domain containing 10 gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20230420 MGI PMID:36062803 1332145 Commd10 COMM domain containing 10 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20200206 MGI PMID:31434684 1332145 Commd10 COMM domain containing 10 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20230420 MGI PMID:36062803 1332145 Commd10 COMM domain containing 10 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20200206 MGI PMID:31434684 1332145 Commd10 COMM domain containing 10 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20180201 MGI PMID:24204913 1332145 Commd10 COMM domain containing 10 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20230420 MGI PMID:36062803 1332145 Commd10 COMM domain containing 10 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20180201 MGI PMID:25129145 1332145 Commd10 COMM domain containing 10 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20180201 MGI PMID:25129145 1332145 Commd10 COMM domain containing 10 gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20180201 MGI PMID:18538592 1332145 Commd10 COMM domain containing 10 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20180201 MGI PMID:18371367 1332145 Commd10 COMM domain containing 10 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20180201 MGI PMID:21339326 1332145 Commd10 COMM domain containing 10 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20180201 MGI PMID:22659386 1332145 Commd10 COMM domain containing 10 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20180201 MGI PMID:23795291 1332145 Commd10 COMM domain containing 10 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20180201 MGI PMID:26001274 1332145 Commd10 COMM domain containing 10 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20180201 MGI PMID:22659386 1332145 Commd10 COMM domain containing 10 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0008998 decreased blood osmolality IAGP N RGD:5509061 20180201 MGI PMID:26001274 1332145 Commd10 COMM domain containing 10 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20180201 MGI PMID:18371367 1332145 Commd10 COMM domain containing 10 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20230330 MGI PMID:35987460 1332145 Commd10 COMM domain containing 10 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20180201 MGI PMID:21844204 1332145 Commd10 COMM domain containing 10 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20230420 MGI PMID:36062803 1332145 Commd10 COMM domain containing 10 gene MP:0009623 enlarged inguinal lymph nodes IAGP N RGD:5509061 20230420 MGI PMID:36062803 1332145 Commd10 COMM domain containing 10 gene MP:0009631 enlarged axillary lymph nodes IAGP N RGD:5509061 20230420 MGI PMID:36062803 1332145 Commd10 COMM domain containing 10 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20230330 MGI PMID:35987460 1332145 Commd10 COMM domain containing 10 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20180201 MGI PMID:24048899 1332145 Commd10 COMM domain containing 10 gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20180201 MGI PMID:25057009 1332145 Commd10 COMM domain containing 10 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20180201 MGI PMID:26001274 1332145 Commd10 COMM domain containing 10 gene MP:0010130 decreased DN1 thymic pro-T cell number IAGP N RGD:5509061 20180201 MGI PMID:21258009 1332145 Commd10 COMM domain containing 10 gene MP:0010132 decreased DN2 thymocyte number IAGP N RGD:5509061 20180201 MGI PMID:21258009 1332145 Commd10 COMM domain containing 10 gene MP:0010134 decreased DN3 thymocyte number IAGP N RGD:5509061 20180201 MGI PMID:21258009 1332145 Commd10 COMM domain containing 10 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20190530 MGI PMID:30237863 1332145 Commd10 COMM domain containing 10 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20180201 MGI PMID:21339326 1332145 Commd10 COMM domain containing 10 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20180201 MGI PMID:18656388 1332145 Commd10 COMM domain containing 10 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:23795291 1332145 Commd10 COMM domain containing 10 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20190103 MGI PMID:30423293 1332145 Commd10 COMM domain containing 10 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1332145 Commd10 COMM domain containing 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332145 Commd10 COMM domain containing 10 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:22659386 1332145 Commd10 COMM domain containing 10 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0011181 increased hematopoietic cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1332145 Commd10 COMM domain containing 10 gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20180201 MGI PMID:22281595 1332145 Commd10 COMM domain containing 10 gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20180201 MGI PMID:25552701 1332145 Commd10 COMM domain containing 10 gene MP:0011746 spleen fibrosis IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0011747 myelofibrosis IAGP N RGD:5509061 20180201 MGI PMID:18160670 1332145 Commd10 COMM domain containing 10 gene MP:0012328 decreased circulating factor VIII level IAGP N RGD:5509061 20180201 MGI PMID:24705491 1332145 Commd10 COMM domain containing 10 gene MP:0012384 abnormal erythrocyte ion transport IAGP N RGD:5509061 20180201 MGI PMID:26001274 1332145 Commd10 COMM domain containing 10 gene MP:0012664 decreased circulating haptoglobin level IAGP N RGD:5509061 20180201 MGI PMID:26001274 1332145 Commd10 COMM domain containing 10 gene MP:0012765 decreased alpha-beta T cell number IAGP N RGD:5509061 20190530 MGI PMID:30237863 1332145 Commd10 COMM domain containing 10 gene MP:0013147 limb paralysis IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0013583 salivary gland degeneration IAGP N RGD:5509061 20220616 MGI PMID:29127143 1332145 Commd10 COMM domain containing 10 gene MP:0013662 decreased myeloid cell number IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0013667 increased immature NK cell number IAGP N RGD:5509061 20210422 MGI PMID:26851218 1332145 Commd10 COMM domain containing 10 gene MP:0013672 decreased mature NK cell number IAGP N RGD:5509061 20210422 MGI PMID:26851218 1332145 Commd10 COMM domain containing 10 gene MP:0013693 abnormal hemopoiesis IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0013693 abnormal hemopoiesis IAGP N RGD:5509061 20190516 MGI PMID:30635284 1332145 Commd10 COMM domain containing 10 gene MP:0013696 increased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1332145 Commd10 COMM domain containing 10 gene MP:0013696 increased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20230330 MGI PMID:35987460 1332145 Commd10 COMM domain containing 10 gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0013704 increased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20180201 MGI PMID:22422825 1332145 Commd10 COMM domain containing 10 gene MP:0013705 decreased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1332145 Commd10 COMM domain containing 10 gene MP:0013892 increased common lymphocyte progenitor cell number IAGP N RGD:5509061 20180201 MGI PMID:22185780 1332145 Commd10 COMM domain containing 10 gene MP:0013893 decreased common lymphocyte progenitor cell number IAGP N RGD:5509061 20220721 MGI PMID:28319097 1332145 Commd10 COMM domain containing 10 gene MP:0020463 increased megakaryocyte progenitor cell number IAGP N RGD:5509061 20190905 MGI PMID:29202466 1332145 Commd10 COMM domain containing 10 gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:28114589 1332145 Commd10 COMM domain containing 10 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200820 MGI PMID:32704094 1332145 Commd10 COMM domain containing 10 gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200820 MGI PMID:32704094 1332145 Commd10 COMM domain containing 10 gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:26001274 1332145 Commd10 COMM domain containing 10 gene MP:0031276 abnormal stress erythropoiesis IAGP N RGD:5509061 20230330 MGI PMID:35987460 1332147 Hmbox1 homeobox containing 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220811 MGI 1332147 Hmbox1 homeobox containing 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23685356 1332147 Hmbox1 homeobox containing 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220811 MGI 1332147 Hmbox1 homeobox containing 1 gene MP:0000745 tremors IEA N RGD:5509061 20240523 MGI 1332147 Hmbox1 homeobox containing 1 gene MP:0001200 thick skin IEA N RGD:5509061 20220811 MGI 1332147 Hmbox1 homeobox containing 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1332147 Hmbox1 homeobox containing 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1332147 Hmbox1 homeobox containing 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1332147 Hmbox1 homeobox containing 1 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20220811 MGI 1332147 Hmbox1 homeobox containing 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20220811 MGI 1332147 Hmbox1 homeobox containing 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20221215 MGI 1332147 Hmbox1 homeobox containing 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1332147 Hmbox1 homeobox containing 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1332147 Hmbox1 homeobox containing 1 gene MP:0009454 impaired contextual conditioning behavior IEA N RGD:5509061 20220811 MGI 1332150 Nolc1 nucleolar and coiled-body phosphoprotein 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20181227 MGI 1332151 Rilpl2 Rab interacting lysosomal protein-like 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1332151 Rilpl2 Rab interacting lysosomal protein-like 2 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1332151 Rilpl2 Rab interacting lysosomal protein-like 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20200310 MGI PMID:17591776 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:12093799 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:12960027 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:17591776 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:9974390 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:12960027 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:21296886 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0001304 cataract IAGP N RGD:5509061 20200310 MGI PMID:21296886 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20200310 MGI PMID:12960027 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:17591776 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:17591776 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:12093799 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0001921 reduced fertility IAGP N RGD:5509061 20200310 MGI PMID:12093799 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:12093799 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:17591776 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21296886 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200310 MGI PMID:17591776 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:17591776 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20200310 MGI PMID:17591776 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:9974390 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20200310 MGI PMID:17591776 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:17591776 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:12960027 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20200310 MGI PMID:17591776 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20200310 MGI PMID:17591776 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0005472 abnormal triiodothyronine level IAGP N RGD:5509061 20200310 MGI PMID:12960027 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20200310 MGI PMID:12960027 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20200310 MGI PMID:12960027 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0005533 increased body temperature IAGP N RGD:5509061 20200310 MGI PMID:12960027 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20200310 MGI PMID:17591776 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20200310 MGI PMID:12093799 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20200310 MGI PMID:12960027 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:12093799 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0009301 decreased parametrial fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:12093799 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:17591776 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20200310 MGI PMID:12093799 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20200310 MGI PMID:12960027 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12093799 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12093799 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21296886 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20200310 MGI PMID:12960027 1332152 Gpd2 glycerol phosphate dehydrogenase 2, mitochondrial gene MP:0030742 increased aspartic acid level IAGP N RGD:5509061 20200310 MGI PMID:17591776 1332153 Mrgprg MAS-related GPR, member G gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1332153 Mrgprg MAS-related GPR, member G gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1332155 Ppif peptidylprolyl isomerase F (cyclophilin F) gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20220811 MGI PMID:35358843 1332155 Ppif peptidylprolyl isomerase F (cyclophilin F) gene MP:0002083 premature death IAGP N RGD:5509061 20150507 MGI PMID:24325796 1332155 Ppif peptidylprolyl isomerase F (cyclophilin F) gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20150507 MGI PMID:24325796 1332155 Ppif peptidylprolyl isomerase F (cyclophilin F) gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:15800626 1332155 Ppif peptidylprolyl isomerase F (cyclophilin F) gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:15800627 1332155 Ppif peptidylprolyl isomerase F (cyclophilin F) gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20220811 MGI PMID:35358843 1332155 Ppif peptidylprolyl isomerase F (cyclophilin F) gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20220811 MGI PMID:35358843 1332155 Ppif peptidylprolyl isomerase F (cyclophilin F) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:15792954 1332155 Ppif peptidylprolyl isomerase F (cyclophilin F) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:15800626 1332155 Ppif peptidylprolyl isomerase F (cyclophilin F) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:15800627 1332155 Ppif peptidylprolyl isomerase F (cyclophilin F) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:16103352 1332155 Ppif peptidylprolyl isomerase F (cyclophilin F) gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:16103352 1332155 Ppif peptidylprolyl isomerase F (cyclophilin F) gene MP:0008407 decreased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:15800626 1332155 Ppif peptidylprolyl isomerase F (cyclophilin F) gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:19524512 1332157 Negr1 neuronal growth regulator 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1332157 Negr1 neuronal growth regulator 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1332157 Negr1 neuronal growth regulator 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1332157 Negr1 neuronal growth regulator 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22844493 1332157 Negr1 neuronal growth regulator 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22844493 1332157 Negr1 neuronal growth regulator 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1332157 Negr1 neuronal growth regulator 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22844493 1332157 Negr1 neuronal growth regulator 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1332157 Negr1 neuronal growth regulator 1 gene MP:0002175 decreased brain weight IEA N RGD:5509061 20210128 MGI 1332157 Negr1 neuronal growth regulator 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22844493 1332157 Negr1 neuronal growth regulator 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:22844493 1332157 Negr1 neuronal growth regulator 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201231 MGI 1332157 Negr1 neuronal growth regulator 1 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22844493 1332157 Negr1 neuronal growth regulator 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22844493 1332157 Negr1 neuronal growth regulator 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20170105 MGI 1332157 Negr1 neuronal growth regulator 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1332157 Negr1 neuronal growth regulator 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:22844493 1332157 Negr1 neuronal growth regulator 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1332159 Orm1 orosomucoid 1 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20201022 MGI PMID:26740279 1332159 Orm1 orosomucoid 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20201022 MGI PMID:26740279 1332160 Hsd17b11 hydroxysteroid (17-beta) dehydrogenase 11 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1332160 Hsd17b11 hydroxysteroid (17-beta) dehydrogenase 11 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1332160 Hsd17b11 hydroxysteroid (17-beta) dehydrogenase 11 gene MP:0002960 decreased urine microalbumin level IEA N RGD:5509061 20210520 MGI 1332160 Hsd17b11 hydroxysteroid (17-beta) dehydrogenase 11 gene MP:0008214 increased immature B cell number IEA N RGD:5509061 20141003 MGI 1332160 Hsd17b11 hydroxysteroid (17-beta) dehydrogenase 11 gene MP:0008500 increased IgG2a level IEA N RGD:5509061 20141003 MGI 1332160 Hsd17b11 hydroxysteroid (17-beta) dehydrogenase 11 gene MP:0011471 decreased urine creatinine level IEA N RGD:5509061 20210128 MGI 1332161 Gldn gliomedin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20188654 1332161 Gldn gliomedin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:20188654 1332161 Gldn gliomedin gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:20188654 1332161 Gldn gliomedin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20188654 1332162 Chn2 chimerin 2 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:22726444 1332162 Chn2 chimerin 2 gene MP:0008960 abnormal axon pruning IAGP N RGD:5509061 20141003 MGI PMID:22726444 1332164 Lin7a lin-7 homolog A, crumbs cell polarity complex component gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:16186258 1332164 Lin7a lin-7 homolog A, crumbs cell polarity complex component gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11104771 1332164 Lin7a lin-7 homolog A, crumbs cell polarity complex component gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16186258 1332164 Lin7a lin-7 homolog A, crumbs cell polarity complex component gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16186258 1332164 Lin7a lin-7 homolog A, crumbs cell polarity complex component gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16186258 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20151119 MGI PMID:18803233 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:10890450 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:10890450 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:10890450 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20150611 MGI PMID:6530139 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:10890450 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20150611 MGI PMID:6530139 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20151119 MGI PMID:18803233 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0002138 abnormal hepatobiliary system morphology IAGP N RGD:5509061 20141003 MGI PMID:10890450 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20150611 MGI PMID:6530139 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0002865 increased growth rate IAGP N RGD:5509061 20141003 MGI PMID:10890450 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0002865 increased growth rate IAGP N RGD:5509061 20141003 MGI PMID:15965258 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20151119 MGI PMID:18803233 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20151119 MGI PMID:18803233 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0004348 long femur IAGP N RGD:5509061 20141003 MGI PMID:10890450 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0004350 long humerus IAGP N RGD:5509061 20141003 MGI PMID:10890450 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0004357 long tibia IAGP N RGD:5509061 20141003 MGI PMID:10890450 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0004357 long tibia IAGP N RGD:5509061 20151119 MGI PMID:18803233 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0004695 increased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:10890450 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20150611 MGI PMID:3957811 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230119 MGI 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20150611 MGI PMID:3957811 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230119 MGI 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20151119 MGI PMID:18803233 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0008162 increased diameter of tibia IAGP N RGD:5509061 20151119 MGI PMID:18803233 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0008831 abnormal insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:10890450 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0008951 long radius IAGP N RGD:5509061 20141003 MGI PMID:10890450 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0009143 abnormal pancreatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:10890450 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20151119 MGI PMID:18803233 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0009517 abnormal salivary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:10890450 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10890450 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20151119 MGI PMID:18803233 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20151119 MGI PMID:18803233 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20151119 MGI PMID:18803233 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0010967 increased compact bone area IAGP N RGD:5509061 20151119 MGI PMID:18803233 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20151119 MGI PMID:18803233 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:22562833 1332166 Socs2 suppressor of cytokine signaling 2 gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:22562833 1332167 Hp1bp3 heterochromatin protein 1, binding protein 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160428 MGI PMID:25662603 1332167 Hp1bp3 heterochromatin protein 1, binding protein 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160428 MGI PMID:25662603 1332167 Hp1bp3 heterochromatin protein 1, binding protein 3 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20160428 MGI PMID:25662603 1332167 Hp1bp3 heterochromatin protein 1, binding protein 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160428 MGI PMID:25662603 1332168 Myom2 myomesin 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1332168 Myom2 myomesin 2 gene MP:0004222 iris synechia IEA N RGD:5509061 20200402 MGI 1332168 Myom2 myomesin 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:15213227 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0001432 abnormal food preference IAGP N RGD:5509061 20141003 MGI PMID:16054071 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16121183 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15213227 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0001934 increased litter size IAGP N RGD:5509061 20141003 MGI PMID:15213227 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12215525 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16121183 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17343295 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0002451 abnormal macrophage physiology IEA N RGD:5509061 20111116 MGI 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0002865 increased growth rate IAGP N RGD:5509061 20141003 MGI PMID:15213227 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17343295 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:15213227 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:12215525 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:15213227 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:15213227 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20210527 MGI PMID:31166980 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20210527 MGI PMID:31166980 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:16121183 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15213227 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:15213227 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15213227 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0020916 increased susceptibility to Herpesvirales infection IEA N RGD:5509061 20200430 MGI 1332170 Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 gene MP:0020931 increased susceptibility to Adenoviridae infection IEA N RGD:5509061 20200430 MGI 1332171 Otos otospiralin gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:15632083 1332171 Otos otospiralin gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15632083 1332171 Otos otospiralin gene MP:0004294 abnormal type II spiral ligament fibrocytes IAGP N RGD:5509061 20141003 MGI PMID:15632083 1332171 Otos otospiralin gene MP:0004296 abnormal type IV spiral ligament fibrocytes IAGP N RGD:5509061 20141003 MGI PMID:15632083 1332171 Otos otospiralin gene MP:0004414 decreased cochlear microphonics IAGP N RGD:5509061 20141003 MGI PMID:15632083 1332171 Otos otospiralin gene MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:15632083 1332173 Spice1 spindle and centriole associated protein 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1332173 Spice1 spindle and centriole associated protein 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20220811 MGI 1332173 Spice1 spindle and centriole associated protein 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0000756 forelimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:23382704 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:10970877 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:23382704 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:23382704 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:10970877 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:10970877 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:11076772 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:11076772 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:23382704 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:23382704 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:11076772 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23382704 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:23382704 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:11076772 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0009180 increased pancreatic delta cell number IAGP N RGD:5509061 20141003 MGI PMID:23382704 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0009186 decreased PP cell number IAGP N RGD:5509061 20141003 MGI PMID:11076772 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0009190 increased pancreatic epsilon cell number IAGP N RGD:5509061 20141003 MGI PMID:23382704 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:11076772 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23382704 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10970877 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23382704 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0021103 abnormal ventral interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:10970877 1332174 Nkx6-1 NK6 homeobox 1 gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:10970877 1332175 Card19 caspase recruitment domain family, member 19 gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20230817 MGI PMID:36961449 1332175 Card19 caspase recruitment domain family, member 19 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20230817 MGI PMID:36961449 1332175 Card19 caspase recruitment domain family, member 19 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20230817 MGI PMID:36961449 1332175 Card19 caspase recruitment domain family, member 19 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20230817 MGI PMID:36961449 1332175 Card19 caspase recruitment domain family, member 19 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20230817 MGI PMID:36961449 1332175 Card19 caspase recruitment domain family, member 19 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20230817 MGI PMID:36961449 1332177 Uts2r urotensin 2 receptor gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20200310 MGI PMID:12770952 1332178 Scfd1 Sec1 family domain containing 1 gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20241017 MGI 1332178 Scfd1 Sec1 family domain containing 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1332178 Scfd1 Sec1 family domain containing 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241017 MGI 1332178 Scfd1 Sec1 family domain containing 1 gene MP:0004964 absent inner cell mass IEA N RGD:5509061 20241017 MGI 1332178 Scfd1 Sec1 family domain containing 1 gene MP:0005028 abnormal trophectoderm morphology IEA N RGD:5509061 20241017 MGI 1332178 Scfd1 Sec1 family domain containing 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 1332178 Scfd1 Sec1 family domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1332178 Scfd1 Sec1 family domain containing 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1332178 Scfd1 Sec1 family domain containing 1 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241017 MGI 1332180 Atg13 autophagy related 13 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20181220 MGI PMID:26644405 1332180 Atg13 autophagy related 13 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1332180 Atg13 autophagy related 13 gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20181220 MGI PMID:26644405 1332180 Atg13 autophagy related 13 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20181220 MGI PMID:26644405 1332180 Atg13 autophagy related 13 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332180 Atg13 autophagy related 13 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20181220 MGI PMID:26644405 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20200402 MGI 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200402 MGI 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0004025 polyploidy IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200402 MGI 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0011705 absent fibroblast proliferation IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0021085 increased DNA replication IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332182 Orc1 origin recognition complex, subunit 1 gene MP:0021086 decreased DNA replication IAGP N RGD:5509061 20221229 MGI PMID:29967292 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0000644 dextrocardia IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0000690 absent spleen IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20180301 MGI PMID:21515572 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20180301 MGI PMID:21515572 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20180301 MGI PMID:21515572 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0002183 gliosis IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0002639 micrognathia IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0003178 left pulmonary isomerism IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0004113 abnormal aortic arch morphology IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0004157 interrupted aortic arch IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0006061 right atrial isomerism IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0008461 left atrial isomerism IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0010403 atrial septal defect IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0010466 vascular ring IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0011249 abdominal situs inversus IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0011250 abdominal situs ambiguus IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0011252 situs inversus totalis IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0011254 superior-inferior ventricles IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0011649 immotile respiratory cilia IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0011668 double outlet right ventricle, Taussig bing type IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20141003 MGI 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0013907 abnormal cerebrospinal fluid flow IAGP N RGD:5509061 20180308 MGI PMID:29317443 1332183 Ccdc39 coiled-coil domain containing 39 gene MP:0031515 l-loop transposition of the great arteries IEA N RGD:5509061 20240118 MGI 1332184 Fbxo38 F-box protein 38 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220721 MGI PMID:35769260 1332184 Fbxo38 F-box protein 38 gene MP:0001258 decreased body length IAGP N RGD:5509061 20220721 MGI PMID:35769260 1332184 Fbxo38 F-box protein 38 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220721 MGI PMID:35769260 1332184 Fbxo38 F-box protein 38 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220721 MGI PMID:35769260 1332184 Fbxo38 F-box protein 38 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220721 MGI PMID:35769260 1332184 Fbxo38 F-box protein 38 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220721 MGI PMID:35769260 1332184 Fbxo38 F-box protein 38 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20220721 MGI PMID:35769260 1332184 Fbxo38 F-box protein 38 gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20220721 MGI PMID:35769260 1332184 Fbxo38 F-box protein 38 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220721 MGI PMID:35769260 1332184 Fbxo38 F-box protein 38 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20220721 MGI PMID:35769260 1332184 Fbxo38 F-box protein 38 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20220721 MGI PMID:35769260 1332184 Fbxo38 F-box protein 38 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20220721 MGI PMID:35769260 1332184 Fbxo38 F-box protein 38 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20220721 MGI PMID:35769260 1332184 Fbxo38 F-box protein 38 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220721 MGI PMID:35769260 1332185 Abcb1b ATP-binding cassette, sub-family B member 1B gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20180719 MGI PMID:10906391 1332185 Abcb1b ATP-binding cassette, sub-family B member 1B gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20180719 MGI PMID:21881209 1332185 Abcb1b ATP-binding cassette, sub-family B member 1B gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20180719 MGI PMID:10906391 1332185 Abcb1b ATP-binding cassette, sub-family B member 1B gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20180719 MGI PMID:10906391 1332185 Abcb1b ATP-binding cassette, sub-family B member 1B gene MP:0008401 abnormal CD8 positive, alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20180719 MGI PMID:10906391 1332185 Abcb1b ATP-binding cassette, sub-family B member 1B gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:10906391 1332185 Abcb1b ATP-binding cassette, sub-family B member 1B gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20180719 MGI PMID:10906391 1332185 Abcb1b ATP-binding cassette, sub-family B member 1B gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20180719 MGI PMID:10906391 1332185 Abcb1b ATP-binding cassette, sub-family B member 1B gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20180719 MGI PMID:16611851 1332185 Abcb1b ATP-binding cassette, sub-family B member 1B gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20180719 MGI PMID:9108099 1332187 Dctn5 dynactin 5 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20160804 MGI 1332187 Dctn5 dynactin 5 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20141003 MGI 1332187 Dctn5 dynactin 5 gene MP:0000433 microcephaly IEA N RGD:5509061 20141003 MGI 1332187 Dctn5 dynactin 5 gene MP:0000452 abnormal mouth morphology IEA N RGD:5509061 20141003 MGI 1332187 Dctn5 dynactin 5 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20141003 MGI 1332187 Dctn5 dynactin 5 gene MP:0001304 cataract IEA N RGD:5509061 20141003 MGI 1332187 Dctn5 dynactin 5 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20141003 MGI 1332187 Dctn5 dynactin 5 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20160804 MGI 1332187 Dctn5 dynactin 5 gene MP:0002639 micrognathia IEA N RGD:5509061 20141003 MGI 1332187 Dctn5 dynactin 5 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1332187 Dctn5 dynactin 5 gene MP:0005157 holoprosencephaly IEA N RGD:5509061 20141003 MGI 1332187 Dctn5 dynactin 5 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20141003 MGI 1332187 Dctn5 dynactin 5 gene MP:0009579 acephaly IEA N RGD:5509061 20141003 MGI 1332187 Dctn5 dynactin 5 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141003 MGI 1332187 Dctn5 dynactin 5 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20141003 MGI 1332187 Dctn5 dynactin 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332187 Dctn5 dynactin 5 gene MP:0011252 situs inversus totalis IEA N RGD:5509061 20141003 MGI 1332187 Dctn5 dynactin 5 gene MP:0011666 double outlet right ventricle, ventricular defect committed to aorta IEA N RGD:5509061 20141003 MGI 1332188 Klhl41 kelch-like 41 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20180531 MGI PMID:28826497 1332188 Klhl41 kelch-like 41 gene MP:0000751 myopathy IAGP N RGD:5509061 20180531 MGI PMID:28826497 1332188 Klhl41 kelch-like 41 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20180531 MGI PMID:28826497 1332188 Klhl41 kelch-like 41 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180531 MGI PMID:28826497 1332188 Klhl41 kelch-like 41 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180531 MGI PMID:28826497 1332191 Ccdc85a coiled-coil domain containing 85A gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0000692 small spleen IEA N RGD:5509061 20210826 MGI 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0001147 small testis IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0001925 male infertility IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20190912 MGI PMID:29335608 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20190912 MGI PMID:29335608 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20190912 MGI PMID:29335608 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20190912 MGI PMID:29335608 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20190912 MGI PMID:29335608 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29335608 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29335608 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29335608 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20190912 MGI PMID:29335608 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0012204 abnormal neuronal stem cell physiology IAGP N RGD:5509061 20190912 MGI PMID:29335608 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0013272 abnormal translation IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0020388 decreased radial glial cell number IAGP N RGD:5509061 20190912 MGI PMID:29335608 1332193 Mettl14 methyltransferase 14, N6-adenosine-methyltransferase subunit gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210422 MGI PMID:28914256 1332198 Sgf29 SAGA complex associated factor 29 gene MP:0000745 tremors IEA N RGD:5509061 20141003 MGI 1332198 Sgf29 SAGA complex associated factor 29 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160804 MGI 1332199 Padi2 peptidyl arginine deiminase, type II gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:22984079 1332199 Padi2 peptidyl arginine deiminase, type II gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22984079 1332199 Padi2 peptidyl arginine deiminase, type II gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1332199 Padi2 peptidyl arginine deiminase, type II gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332200 Tpd52l2 tumor protein D52-like 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1332200 Tpd52l2 tumor protein D52-like 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20160922 MGI PMID:24652767 1332202 Myl12b myosin, light chain 12B, regulatory gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20160804 MGI 1332202 Myl12b myosin, light chain 12B, regulatory gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1332202 Myl12b myosin, light chain 12B, regulatory gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20160804 MGI 1332202 Myl12b myosin, light chain 12B, regulatory gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20160804 MGI 1332202 Myl12b myosin, light chain 12B, regulatory gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1332202 Myl12b myosin, light chain 12B, regulatory gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20160804 MGI 1332202 Myl12b myosin, light chain 12B, regulatory gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160804 MGI 1332202 Myl12b myosin, light chain 12B, regulatory gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20160804 MGI 1332202 Myl12b myosin, light chain 12B, regulatory gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160804 MGI 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20160114 MGI PMID:17906635 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0001513 limb grasping IEA N RGD:5509061 20170105 MGI 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210128 MGI 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20160114 MGI PMID:17906635 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160114 MGI PMID:17906635 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20160114 MGI PMID:17906635 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20160114 MGI PMID:17906635 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0003858 enhanced coordination IEA N RGD:5509061 20141003 MGI 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20160114 MGI PMID:17906635 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20141003 MGI 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20160114 MGI PMID:17906635 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20160114 MGI PMID:17906635 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20160114 MGI PMID:17906635 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20160114 MGI PMID:17906635 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20160114 MGI PMID:17906635 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20160114 MGI PMID:17906635 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332205 Elovl6 ELOVL fatty acid elongase 6 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:17906635 1332206 Mettl13 methyltransferase 13, eEF1A lysine and N-terminal methyltransferase gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20220721 MGI PMID:30178547 1332206 Mettl13 methyltransferase 13, eEF1A lysine and N-terminal methyltransferase gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220721 MGI PMID:30178547 1332206 Mettl13 methyltransferase 13, eEF1A lysine and N-terminal methyltransferase gene MP:0001925 male infertility IAGP N RGD:5509061 20220721 MGI PMID:30178547 1332206 Mettl13 methyltransferase 13, eEF1A lysine and N-terminal methyltransferase gene MP:0031287 bilateral cryptorchism IAGP N RGD:5509061 20220721 MGI PMID:30178547 1332207 Acvr1b activin A receptor, type 1B gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20160421 MGI 1332207 Acvr1b activin A receptor, type 1B gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1332207 Acvr1b activin A receptor, type 1B gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1332207 Acvr1b activin A receptor, type 1B gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 1332207 Acvr1b activin A receptor, type 1B gene MP:0001147 small testis IEA N RGD:5509061 20160811 MGI 1332207 Acvr1b activin A receptor, type 1B gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9512518 1332207 Acvr1b activin A receptor, type 1B gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:9512518 1332207 Acvr1b activin A receptor, type 1B gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20141003 MGI PMID:9512518 1332207 Acvr1b activin A receptor, type 1B gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9512518 1332207 Acvr1b activin A receptor, type 1B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 1332207 Acvr1b activin A receptor, type 1B gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:16564040 1332207 Acvr1b activin A receptor, type 1B gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16564040 1332207 Acvr1b activin A receptor, type 1B gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:9512518 1332207 Acvr1b activin A receptor, type 1B gene MP:0002768 small adrenal glands IEA N RGD:5509061 20160811 MGI 1332207 Acvr1b activin A receptor, type 1B gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0003875 abnormal hair follicle regression IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:9512518 1332207 Acvr1b activin A receptor, type 1B gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9512518 1332207 Acvr1b activin A receptor, type 1B gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:16564040 1332207 Acvr1b activin A receptor, type 1B gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0009535 abnormal skin sebaceous gland morphology IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0009715 thick epidermis stratum basale IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0010096 abnormal incisor color IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0010126 abnormal distal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9512518 1332207 Acvr1b activin A receptor, type 1B gene MP:0010680 abnormal skin adnexa physiology IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0010699 dilated hair follicle IAGP N RGD:5509061 20141003 MGI PMID:21191412 1332207 Acvr1b activin A receptor, type 1B gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9512518 1332207 Acvr1b activin A receptor, type 1B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23109354 1332207 Acvr1b activin A receptor, type 1B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9512518 1332207 Acvr1b activin A receptor, type 1B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1332207 Acvr1b activin A receptor, type 1B gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9512518 1332207 Acvr1b activin A receptor, type 1B gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:16564040 1332207 Acvr1b activin A receptor, type 1B gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1332207 Acvr1b activin A receptor, type 1B gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:21191412 1332209 Pxk PX domain containing serine/threonine kinase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1332209 Pxk PX domain containing serine/threonine kinase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1332209 Pxk PX domain containing serine/threonine kinase gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1332209 Pxk PX domain containing serine/threonine kinase gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220519 MGI 1332209 Pxk PX domain containing serine/threonine kinase gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1332209 Pxk PX domain containing serine/threonine kinase gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210520 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220811 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000633 abnormal pituitary gland morphology IEA N RGD:5509061 20111116 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000692 small spleen IEA N RGD:5509061 20220811 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000745 tremors IEA N RGD:5509061 20111116 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17135419 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17135419 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:4111750 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17320843 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:17320843 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:14660671 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001134 absent corpus luteum IEA N RGD:5509061 20111116 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220519 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001148 enlarged testis IEA N RGD:5509061 20220519 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20220811 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14660671 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17320843 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14660671 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220519 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001304 cataract IEA N RGD:5509061 20220519 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:14660671 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11487633 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:14660671 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20150507 MGI PMID:23732642 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20230601 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:14660671 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20111116 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230601 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:1195260 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:4111750 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001824 abnormal thymus involution IEA N RGD:5509061 20150326 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001867 rhinitis IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001921 reduced fertility IEA N RGD:5509061 20111116 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001922 reduced male fertility IEA N RGD:5509061 20111116 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:1195260 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14660671 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220811 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:14660671 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:4111750 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20141003 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20160218 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:4111750 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002188 small heart IEA N RGD:5509061 20220811 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20150507 MGI PMID:23732642 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17135419 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:14660671 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0002989 small kidney IEA N RGD:5509061 20220811 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20220519 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:11487633 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0003216 absence seizures IAGP N RGD:5509061 20150507 MGI PMID:23732642 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:11487633 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220519 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:17320843 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0003994 abnormal dorsal spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0004706 short vertebral body IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:14660671 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:17320843 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20220519 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:11487633 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:14660671 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0005202 lethargy IEA N RGD:5509061 20111116 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15331424 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:17135419 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:5456441 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:9349522 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0008035 behavioral arrest IAGP N RGD:5509061 20141003 MGI PMID:14660671 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0008333 absent lactotrophs IAGP N RGD:5509061 20141003 MGI PMID:1195260 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0008770 decreased survivor rate IEA N RGD:5509061 20111116 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:11487633 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:4111750 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20150507 MGI PMID:23732642 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0009460 skeletal muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:4177347 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220519 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14660671 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:17135419 1332210 Cacna2d2 calcium channel, voltage-dependent, alpha 2/delta subunit 2 gene MP:0020533 decreased pons size IAGP N RGD:5509061 20180301 MGI PMID:4177347 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000274 enlarged heart IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000275 heart hyperplasia IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000292 distended pericardium IAGP N RGD:5509061 20180719 MGI PMID:9883720 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20180719 MGI PMID:8700526 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20180719 MGI PMID:8700526 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20180719 MGI PMID:2065352 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20180719 MGI PMID:8700526 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180719 MGI PMID:2065352 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20180719 MGI PMID:8700526 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20180719 MGI PMID:2065352 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20180719 MGI PMID:8806812 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20180719 MGI PMID:21212806 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000852 small cerebellum IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20180719 MGI PMID:8700526 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20180719 MGI PMID:9883720 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0001304 cataract IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0001785 edema IAGP N RGD:5509061 20180719 MGI PMID:9883720 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0001787 pericardial edema IAGP N RGD:5509061 20180719 MGI PMID:9883720 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0001861 lung inflammation IAGP N RGD:5509061 20180719 MGI PMID:2065352 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20180719 MGI PMID:8700526 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20180719 MGI PMID:7671324 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:2554496 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20180719 MGI PMID:19299624 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20180719 MGI PMID:8700526 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20180719 MGI PMID:9883720 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002763 ectopic Bergmann glia cells IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002833 increased heart weight IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20180719 MGI PMID:2065352 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20180719 MGI PMID:2065352 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20180719 MGI PMID:9883720 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0004545 enlarged esophagus IAGP N RGD:5509061 20180719 MGI PMID:2065352 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:2065352 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180719 MGI PMID:2065352 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20180719 MGI PMID:2065352 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0005150 cachexia IAGP N RGD:5509061 20180719 MGI PMID:2065352 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20241114 MGI PMID:31237944 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0005244 hemopericardium IAGP N RGD:5509061 20180719 MGI PMID:9883720 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20180719 MGI PMID:9883720 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0006098 absent cerebellar lobules IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0006321 increased myocardial fiber number IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20180719 MGI PMID:19299624 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20180719 MGI PMID:7671324 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20180719 MGI PMID:7671324 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20180719 MGI PMID:7671324 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20180719 MGI PMID:8700526 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20180719 MGI PMID:2065352 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20180719 MGI PMID:8700526 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180719 MGI PMID:21212806 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0009216 abnormal peritoneum morphology IAGP N RGD:5509061 20180719 MGI PMID:9883720 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0009268 absent cerebellum fissure IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20180719 MGI PMID:19299624 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20180719 MGI PMID:7671324 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20180719 MGI PMID:8806812 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20180719 MGI PMID:9883720 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20180719 MGI PMID:15987940 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0009978 abnormal cerebellum white matter morphology IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:2065352 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:2065353 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:8700526 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:9883720 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:9883720 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:9883720 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0011394 increased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20180719 MGI PMID:20080568 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20180719 MGI PMID:9883720 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0013551 decreased cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20180719 MGI PMID:20980600 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:19299624 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20190704 MGI PMID:9883720 1332211 Abl1 c-abl oncogene 1, non-receptor tyrosine kinase gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:20080568 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18658108 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20200123 MGI PMID:27681422 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200123 MGI PMID:27681422 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18802071 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0001891 hydrocephaly IEA N RGD:5509061 20170105 MGI 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20170105 MGI 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17983582 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20200123 MGI PMID:27681422 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20200123 MGI PMID:27681422 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200123 MGI PMID:27681422 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200123 MGI PMID:27681422 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18802071 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18802071 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:18802071 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:18658108 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17983582 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20200123 MGI PMID:27681422 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17983582 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20200123 MGI PMID:27681422 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20200123 MGI PMID:27681422 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200123 MGI PMID:27681422 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:27681422 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:18658108 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17983582 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18658108 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20200123 MGI PMID:27681422 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200123 MGI PMID:27681422 1332214 Nampt nicotinamide phosphoribosyltransferase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1332215 Lacc1 laccase domain containing 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20180315 MGI PMID:27478939 1332215 Lacc1 laccase domain containing 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20180315 MGI PMID:27478939 1332215 Lacc1 laccase domain containing 1 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20180315 MGI PMID:27478939 1332215 Lacc1 laccase domain containing 1 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20180315 MGI PMID:27478939 1332215 Lacc1 laccase domain containing 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20180315 MGI PMID:27478939 1332215 Lacc1 laccase domain containing 1 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20180315 MGI PMID:27478939 1332215 Lacc1 laccase domain containing 1 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20180315 MGI PMID:27478939 1332215 Lacc1 laccase domain containing 1 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20180315 MGI PMID:27478939 1332215 Lacc1 laccase domain containing 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20180315 MGI PMID:27478939 1332215 Lacc1 laccase domain containing 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20180315 MGI PMID:27478939 1332215 Lacc1 laccase domain containing 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20180315 MGI PMID:27478939 1332215 Lacc1 laccase domain containing 1 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20180315 MGI PMID:27478939 1332216 Samm50 SAMM50 sorting and assembly machinery component gene MP:0001523 impaired righting response IEA N RGD:5509061 20230119 MGI 1332216 Samm50 SAMM50 sorting and assembly machinery component gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230119 MGI 1332216 Samm50 SAMM50 sorting and assembly machinery component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1332218 Use1 unconventional SNARE in the ER 1 homolog (S. cerevisiae) gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:19188447 1332218 Use1 unconventional SNARE in the ER 1 homolog (S. cerevisiae) gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19188447 1332218 Use1 unconventional SNARE in the ER 1 homolog (S. cerevisiae) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19188447 1332218 Use1 unconventional SNARE in the ER 1 homolog (S. cerevisiae) gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19188447 1332218 Use1 unconventional SNARE in the ER 1 homolog (S. cerevisiae) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19188447 1332218 Use1 unconventional SNARE in the ER 1 homolog (S. cerevisiae) gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19188447 1332218 Use1 unconventional SNARE in the ER 1 homolog (S. cerevisiae) gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:19188447 1332218 Use1 unconventional SNARE in the ER 1 homolog (S. cerevisiae) gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:19188447 1332218 Use1 unconventional SNARE in the ER 1 homolog (S. cerevisiae) gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:19188447 1332218 Use1 unconventional SNARE in the ER 1 homolog (S. cerevisiae) gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19188447 1332218 Use1 unconventional SNARE in the ER 1 homolog (S. cerevisiae) gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:19188447 1332218 Use1 unconventional SNARE in the ER 1 homolog (S. cerevisiae) gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:19188447 1332218 Use1 unconventional SNARE in the ER 1 homolog (S. cerevisiae) gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20161013 MGI PMID:19188447 1332219 Car3 carbonic anhydrase 3 gene MP:0001523 impaired righting response IEA N RGD:5509061 20230601 MGI 1332219 Car3 carbonic anhydrase 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230601 MGI 1332219 Car3 carbonic anhydrase 3 gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15509796 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18056838 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18056838 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24121508 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:18096761 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20185832 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:20733101 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:21270129 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17646578 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18056838 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:18056838 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:17646578 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18056838 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:18056838 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:18096761 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20185832 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18096761 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0001598 abnormal blood viscosity IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17646578 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18096761 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18056838 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18096761 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20733101 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24121508 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18056838 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002450 abnormal lymph organ development IAGP N RGD:5509061 20141003 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18056838 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22464323 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22955912 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:24121508 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:18096761 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:20733101 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:24121508 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:18056838 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:18096761 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:24121508 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:24121508 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:21270129 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:24121508 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21270129 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:17646578 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20733101 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17646578 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0004120 cardiac ischemia IAGP N RGD:5509061 20141003 MGI PMID:18096761 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:20185832 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:20733101 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:18096761 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:20733101 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:20733101 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:17646578 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:24121508 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17646578 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18096761 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:20733101 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:18056838 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:24121508 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0005575 increased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:24121508 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0005585 increased tidal volume IAGP N RGD:5509061 20141003 MGI PMID:24121508 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20733101 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17646578 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20733101 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20733101 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:22955912 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20240118 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18056838 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18056838 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:24121508 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:20733101 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:20733101 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0010127 hypervolemia IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21270129 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19217150 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24121508 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21270129 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18096761 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:18056838 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:18096761 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0011286 decreased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:22955912 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0011287 increased erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:24121508 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:20733101 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20240118 MGI PMID:16966370 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0012397 abnormal nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23264599 1332220 Egln1 egl-9 family hypoxia-inducible factor 1 gene MP:0020327 abnormal capillary branching pattern IAGP N RGD:5509061 20160714 MGI PMID:17646578 1332221 Krt13 keratin 13 gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20210325 MGI PMID:32758484 1332221 Krt13 keratin 13 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20210325 MGI PMID:32758484 1332221 Krt13 keratin 13 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20210325 MGI PMID:32758484 1332221 Krt13 keratin 13 gene MP:0030179 abnormal oral epithelium morphology IAGP N RGD:5509061 20210325 MGI PMID:32758484 1332223 Tmem178 transmembrane protein 178 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20161103 MGI PMID:26644563 1332223 Tmem178 transmembrane protein 178 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20161103 MGI PMID:26644563 1332223 Tmem178 transmembrane protein 178 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20161103 MGI PMID:26644563 1332223 Tmem178 transmembrane protein 178 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20161103 MGI PMID:26644563 1332223 Tmem178 transmembrane protein 178 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20161103 MGI PMID:26644563 1332223 Tmem178 transmembrane protein 178 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20161103 MGI PMID:26644563 1332223 Tmem178 transmembrane protein 178 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20161103 MGI PMID:26644563 1332223 Tmem178 transmembrane protein 178 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20161103 MGI PMID:26644563 1332223 Tmem178 transmembrane protein 178 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20161103 MGI PMID:26644563 1332223 Tmem178 transmembrane protein 178 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20161103 MGI PMID:26644563 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220922 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000130 abnormal trabecular bone morphology IEA N RGD:5509061 20111116 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20231207 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000274 enlarged heart IEA N RGD:5509061 20231207 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20231207 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20231207 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0000755 hindlimb paralysis IEA N RGD:5509061 20111116 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0001293 anophthalmia IEA N RGD:5509061 20231207 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0001304 cataract IEA N RGD:5509061 20111116 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20111116 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20410296 1332224 Gulo gulonolactone (L-) oxidase gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20111116 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0003116 rickets IEA N RGD:5509061 20111116 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20231207 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20240523 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0005245 hemarthrosis IAGP N RGD:5509061 20201015 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20231207 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0009864 abnormal aorta endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0011229 abnormal vitamin C level IAGP N RGD:5509061 20141003 MGI PMID:10639167 1332224 Gulo gulonolactone (L-) oxidase gene MP:0011229 abnormal vitamin C level IAGP N RGD:5509061 20141003 MGI PMID:20410296 1332224 Gulo gulonolactone (L-) oxidase gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:11062347 1332224 Gulo gulonolactone (L-) oxidase gene MP:0030827 femur fracture IEA N RGD:5509061 20181018 MGI 1332224 Gulo gulonolactone (L-) oxidase gene MP:0030884 rachitic rosary IAGP N RGD:5509061 20181101 MGI PMID:20410296 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0001393 ataxia IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0009974 decreased cerebral cortex pyramidal cell number IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200310 MGI 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200310 MGI 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332226 Atp6v0a1 ATPase, H+ transporting, lysosomal V0 subunit A1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20210603 MGI PMID:33833240 1332227 Pdcd2l programmed cell death 2-like gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210715 MGI PMID:33055224 1332227 Pdcd2l programmed cell death 2-like gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20210715 MGI PMID:33055224 1332228 2310061I04Rik RIKEN cDNA 2310061I04 gene gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220519 MGI 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0001393 ataxia IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0001513 limb grasping IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0002083 premature death IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20220811 MGI 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0008918 microgliosis IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0010732 abnormal node of Ranvier morphology IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0014331 abnormal Purkinje cell mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:28376086 1332229 Slc25a46 solute carrier family 25, member 46 gene MP:0020339 abnormal retina ganglion cell dendrite morphology IAGP N RGD:5509061 20190418 MGI PMID:28376086 1332231 Ppil3 peptidylprolyl isomerase (cyclophilin)-like 3 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20160421 MGI 1332231 Ppil3 peptidylprolyl isomerase (cyclophilin)-like 3 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1332231 Ppil3 peptidylprolyl isomerase (cyclophilin)-like 3 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1332231 Ppil3 peptidylprolyl isomerase (cyclophilin)-like 3 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1332231 Ppil3 peptidylprolyl isomerase (cyclophilin)-like 3 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20170105 MGI 1332232 Zhx3 zinc fingers and homeoboxes 3 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 1332232 Zhx3 zinc fingers and homeoboxes 3 gene MP:0001257 increased body length IEA N RGD:5509061 20150430 MGI 1332232 Zhx3 zinc fingers and homeoboxes 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1332232 Zhx3 zinc fingers and homeoboxes 3 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20240627 MGI 1332232 Zhx3 zinc fingers and homeoboxes 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150430 MGI 1332232 Zhx3 zinc fingers and homeoboxes 3 gene MP:0004357 long tibia IEA N RGD:5509061 20160114 MGI 1332232 Zhx3 zinc fingers and homeoboxes 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20240627 MGI 1332232 Zhx3 zinc fingers and homeoboxes 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1332232 Zhx3 zinc fingers and homeoboxes 3 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 1332232 Zhx3 zinc fingers and homeoboxes 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1332232 Zhx3 zinc fingers and homeoboxes 3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1332232 Zhx3 zinc fingers and homeoboxes 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332232 Zhx3 zinc fingers and homeoboxes 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1332234 Atxn3 ataxin 3 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20160317 MGI PMID:25301414 1332234 Atxn3 ataxin 3 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20160317 MGI PMID:25301414 1332234 Atxn3 ataxin 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160317 MGI PMID:25301414 1332234 Atxn3 ataxin 3 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17764659 1332234 Atxn3 ataxin 3 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20160317 MGI PMID:25301414 1332234 Atxn3 ataxin 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:17764659 1332234 Atxn3 ataxin 3 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20160317 MGI PMID:25301414 1332234 Atxn3 ataxin 3 gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20151015 MGI PMID:25320121 1332234 Atxn3 ataxin 3 gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20160317 MGI PMID:25301414 1332234 Atxn3 ataxin 3 gene MP:0004794 increased anti-nuclear antigen antibody level IEA N RGD:5509061 20201022 MGI 1332234 Atxn3 ataxin 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20210128 MGI 1332234 Atxn3 ataxin 3 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20201022 MGI 1332234 Atxn3 ataxin 3 gene MP:0011975 neuronal cytoplasmic inclusions IAGP N RGD:5509061 20151015 MGI PMID:25320121 1332234 Atxn3 ataxin 3 gene MP:0011975 neuronal cytoplasmic inclusions IAGP N RGD:5509061 20160317 MGI PMID:25301414 1332234 Atxn3 ataxin 3 gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:25301414 1332235 Sla src-like adaptor gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11567635 1332235 Sla src-like adaptor gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21220694 1332235 Sla src-like adaptor gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11567635 1332235 Sla src-like adaptor gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:11567635 1332235 Sla src-like adaptor gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11567635 1332235 Sla src-like adaptor gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21220694 1332235 Sla src-like adaptor gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21220694 1332235 Sla src-like adaptor gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:21220694 1332239 Arhgap44 Rho GTPase activating protein 44 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1332239 Arhgap44 Rho GTPase activating protein 44 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180111 MGI PMID:26969129 1332239 Arhgap44 Rho GTPase activating protein 44 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20180111 MGI PMID:26969129 1332239 Arhgap44 Rho GTPase activating protein 44 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20180111 MGI PMID:26969129 1332239 Arhgap44 Rho GTPase activating protein 44 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20180111 MGI PMID:26969129 1332239 Arhgap44 Rho GTPase activating protein 44 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20180111 MGI PMID:26969129 1332239 Arhgap44 Rho GTPase activating protein 44 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20180111 MGI PMID:26969129 1332239 Arhgap44 Rho GTPase activating protein 44 gene MP:0020512 abnormal dendritic mushroom spine morphology IAGP N RGD:5509061 20180111 MGI PMID:26969129 1332239 Arhgap44 Rho GTPase activating protein 44 gene MP:0020513 abnormal dendritic stubby spine morphology IAGP N RGD:5509061 20180111 MGI PMID:26969129 1332240 Abraxas1 BRCA1 A complex subunit gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20190523 MGI PMID:25066119 1332240 Abraxas1 BRCA1 A complex subunit gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20190523 MGI PMID:25066119 1332240 Abraxas1 BRCA1 A complex subunit gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20190523 MGI PMID:25066119 1332240 Abraxas1 BRCA1 A complex subunit gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20190523 MGI PMID:25066119 1332240 Abraxas1 BRCA1 A complex subunit gene MP:0002083 premature death IAGP N RGD:5509061 20190523 MGI PMID:25066119 1332240 Abraxas1 BRCA1 A complex subunit gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20190523 MGI PMID:25066119 1332240 Abraxas1 BRCA1 A complex subunit gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20190523 MGI PMID:25066119 1332240 Abraxas1 BRCA1 A complex subunit gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20190523 MGI PMID:25066119 1332240 Abraxas1 BRCA1 A complex subunit gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20190523 MGI PMID:25066119 1332240 Abraxas1 BRCA1 A complex subunit gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20190523 MGI PMID:25066119 1332240 Abraxas1 BRCA1 A complex subunit gene MP:0014040 increased cellular sensitivity to DNA damaging agents IAGP N RGD:5509061 20190523 MGI PMID:25066119 1332241 Tefm transcription elongation factor, mitochondrial gene MP:0000274 enlarged heart IAGP N RGD:5509061 20191003 MGI PMID:31036713 1332241 Tefm transcription elongation factor, mitochondrial gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20191003 MGI PMID:31036713 1332241 Tefm transcription elongation factor, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191003 MGI PMID:31036713 1332241 Tefm transcription elongation factor, mitochondrial gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20191003 MGI PMID:31036713 1332241 Tefm transcription elongation factor, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20191003 MGI PMID:31036713 1332241 Tefm transcription elongation factor, mitochondrial gene MP:0002833 increased heart weight IAGP N RGD:5509061 20191003 MGI PMID:31036713 1332241 Tefm transcription elongation factor, mitochondrial gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20191003 MGI PMID:31036713 1332241 Tefm transcription elongation factor, mitochondrial gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20191003 MGI PMID:31036713 1332241 Tefm transcription elongation factor, mitochondrial gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20191003 MGI PMID:31036713 1332241 Tefm transcription elongation factor, mitochondrial gene MP:0012081 absent heart tube IAGP N RGD:5509061 20191003 MGI PMID:31036713 1332241 Tefm transcription elongation factor, mitochondrial gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20191003 MGI PMID:31036713 1332242 Sipa1l1 signal-induced proliferation-associated 1 like 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20240509 MGI PMID:35121636 1332242 Sipa1l1 signal-induced proliferation-associated 1 like 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20240509 MGI PMID:35121636 1332242 Sipa1l1 signal-induced proliferation-associated 1 like 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1332242 Sipa1l1 signal-induced proliferation-associated 1 like 1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20240509 MGI PMID:35121636 1332242 Sipa1l1 signal-induced proliferation-associated 1 like 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20240509 MGI PMID:35121636 1332242 Sipa1l1 signal-induced proliferation-associated 1 like 1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20240509 MGI PMID:35121636 1332242 Sipa1l1 signal-induced proliferation-associated 1 like 1 gene MP:0002807 abnormal eye blink conditioning behavior IAGP N RGD:5509061 20240509 MGI PMID:35121636 1332242 Sipa1l1 signal-induced proliferation-associated 1 like 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20240509 MGI PMID:35121636 1332242 Sipa1l1 signal-induced proliferation-associated 1 like 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20181227 MGI 1332242 Sipa1l1 signal-induced proliferation-associated 1 like 1 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20240509 MGI PMID:35121636 1332242 Sipa1l1 signal-induced proliferation-associated 1 like 1 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20240509 MGI PMID:35121636 1332242 Sipa1l1 signal-induced proliferation-associated 1 like 1 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20240509 MGI PMID:35121636 1332242 Sipa1l1 signal-induced proliferation-associated 1 like 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1332242 Sipa1l1 signal-induced proliferation-associated 1 like 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20240509 MGI PMID:35121636 1332242 Sipa1l1 signal-induced proliferation-associated 1 like 1 gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20240509 MGI PMID:35121636 1332244 Tmub2 transmembrane and ubiquitin-like domain containing 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1332244 Tmub2 transmembrane and ubiquitin-like domain containing 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1332244 Tmub2 transmembrane and ubiquitin-like domain containing 2 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1332244 Tmub2 transmembrane and ubiquitin-like domain containing 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220811 MGI 1332244 Tmub2 transmembrane and ubiquitin-like domain containing 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20231207 MGI 1332244 Tmub2 transmembrane and ubiquitin-like domain containing 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 1332244 Tmub2 transmembrane and ubiquitin-like domain containing 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1332244 Tmub2 transmembrane and ubiquitin-like domain containing 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1332245 Asic3 acid-sensing ion channel 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 1332245 Asic3 acid-sensing ion channel 3 gene MP:0000601 small liver IEA N RGD:5509061 20230601 MGI 1332245 Asic3 acid-sensing ion channel 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1332245 Asic3 acid-sensing ion channel 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1332245 Asic3 acid-sensing ion channel 3 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19117938 1332245 Asic3 acid-sensing ion channel 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20230601 MGI 1332245 Asic3 acid-sensing ion channel 3 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:14659506 1332245 Asic3 acid-sensing ion channel 3 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:12060708 1332245 Asic3 acid-sensing ion channel 3 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:17553498 1332245 Asic3 acid-sensing ion channel 3 gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:12060708 1332245 Asic3 acid-sensing ion channel 3 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:12060708 1332245 Asic3 acid-sensing ion channel 3 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19117938 1332245 Asic3 acid-sensing ion channel 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230601 MGI 1332245 Asic3 acid-sensing ion channel 3 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20230601 MGI 1332245 Asic3 acid-sensing ion channel 3 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:17531389 1332245 Asic3 acid-sensing ion channel 3 gene MP:0005407 hyperalgesia IAGP N RGD:5509061 20141003 MGI PMID:11754838 1332245 Asic3 acid-sensing ion channel 3 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:14659506 1332245 Asic3 acid-sensing ion channel 3 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19117938 1332245 Asic3 acid-sensing ion channel 3 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19117938 1332245 Asic3 acid-sensing ion channel 3 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19117938 1332245 Asic3 acid-sensing ion channel 3 gene MP:0008103 amacrine cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19117938 1332245 Asic3 acid-sensing ion channel 3 gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:19117938 1332245 Asic3 acid-sensing ion channel 3 gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:19117938 1332245 Asic3 acid-sensing ion channel 3 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:19117938 1332245 Asic3 acid-sensing ion channel 3 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:19117938 1332245 Asic3 acid-sensing ion channel 3 gene MP:0008532 decreased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:12060708 1332245 Asic3 acid-sensing ion channel 3 gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:19117938 1332245 Asic3 acid-sensing ion channel 3 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:19117938 1332245 Asic3 acid-sensing ion channel 3 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17553498 1332245 Asic3 acid-sensing ion channel 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1332245 Asic3 acid-sensing ion channel 3 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20230601 MGI 1332245 Asic3 acid-sensing ion channel 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15051137 1332250 Epn1 epsin 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:23187125 1332250 Epn1 epsin 1 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23187125 1332250 Epn1 epsin 1 gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20160623 MGI PMID:23187125 1332250 Epn1 epsin 1 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23187125 1332250 Epn1 epsin 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23187125 1332250 Epn1 epsin 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23187125 1332250 Epn1 epsin 1 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:23187125 1332250 Epn1 epsin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19666558 1332250 Epn1 epsin 1 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:23187125 1332250 Epn1 epsin 1 gene MP:0020161 increased vascular endothelial cell proliferation IAGP N RGD:5509061 20160623 MGI PMID:23187125 1332251 Scn3b sodium channel, voltage-gated, type III, beta gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:19351516 1332251 Scn3b sodium channel, voltage-gated, type III, beta gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20150108 MGI 1332251 Scn3b sodium channel, voltage-gated, type III, beta gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:19351516 1332251 Scn3b sodium channel, voltage-gated, type III, beta gene MP:0004510 myositis IAGP N RGD:5509061 20190124 MGI PMID:25340873 1332251 Scn3b sodium channel, voltage-gated, type III, beta gene MP:0004609 vertebral fusion IEA N RGD:5509061 20201231 MGI 1332251 Scn3b sodium channel, voltage-gated, type III, beta gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:19351516 1332251 Scn3b sodium channel, voltage-gated, type III, beta gene MP:0011157 abnormal hypodermis muscle layer morphology IAGP N RGD:5509061 20190124 MGI PMID:25340873 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22711987 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15572694 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22711987 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19956719 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22711987 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:22711987 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0003437 abnormal carotid body morphology IAGP N RGD:5509061 20141003 MGI PMID:22711987 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0003438 abnormal carotid body physiology IAGP N RGD:5509061 20141003 MGI PMID:15572694 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22711987 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0005039 hypoxia IAGP N RGD:5509061 20180111 MGI PMID:28204537 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:22711987 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0005563 abnormal hemoglobin content IAGP N RGD:5509061 20180111 MGI PMID:28204537 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22711987 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0008504 abnormal adrenal chromaffin cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22711987 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22711987 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:22711987 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:15572694 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19956719 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15572694 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0020840 abnormal type I cell of carotid body morphology IAGP N RGD:5509061 20181101 MGI PMID:15572694 1332252 Sdhd succinate dehydrogenase complex, subunit D, integral membrane protein gene MP:0020843 abnormal type I cell of carotid body physiology IAGP N RGD:5509061 20181101 MGI PMID:15572694 1332253 Pomgnt2 protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20151001 MGI PMID:24256719 1332253 Pomgnt2 protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20151001 MGI PMID:24256719 1332253 Pomgnt2 protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2 gene MP:0004273 abnormal basal lamina morphology IAGP N RGD:5509061 20151001 MGI PMID:24256719 1332253 Pomgnt2 protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20151001 MGI PMID:24256719 1332253 Pomgnt2 protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20151001 MGI PMID:24256719 1332253 Pomgnt2 protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20151001 MGI PMID:24256719 1332253 Pomgnt2 protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20151001 MGI PMID:24256719 1332253 Pomgnt2 protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20151001 MGI PMID:24256719 1332253 Pomgnt2 protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2 gene MP:0020391 radial glial endfoot detachment IAGP N RGD:5509061 20161117 MGI PMID:24256719 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:16648858 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:16648858 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:24550287 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16648858 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:16087873 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:17987665 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:19439667 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:16648858 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:16648858 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:17987665 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:16648858 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16648858 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17987665 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:20418913 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:16648858 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16087873 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19439667 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16648858 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:16648858 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:17987665 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:16648858 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16087873 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16648858 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17987665 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20418913 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24550287 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17987665 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002676 uterus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17987665 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:24550287 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0002936 joint swelling IAGP N RGD:5509061 20141003 MGI PMID:24550287 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:16087873 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:24550287 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0003711 pathological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:16087873 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16648858 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16648858 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19439667 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20418913 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:20418913 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:17987665 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:19439667 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:20418913 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0005488 bronchial epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:24550287 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:24550287 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17987665 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19439667 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20418913 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16648858 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0010887 pale lung IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0010910 bronchiolar epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0010942 abnormal respiratory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0010945 lung epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17987665 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19710174 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0011692 increased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:24550287 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0013401 increased endometrial gland number IAGP N RGD:5509061 20141218 MGI PMID:19439667 1332254 Errfi1 ERBB receptor feedback inhibitor 1 gene MP:0030332 accelerated temporomandibular joint osteoarthritis IAGP N RGD:5509061 20171109 MGI PMID:16087873 1332256 Zfp622 zinc finger protein 622 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240926 MGI 1332256 Zfp622 zinc finger protein 622 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20240926 MGI 1332256 Zfp622 zinc finger protein 622 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1332256 Zfp622 zinc finger protein 622 gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20240926 MGI 1332256 Zfp622 zinc finger protein 622 gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20240926 MGI 1332256 Zfp622 zinc finger protein 622 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230601 MGI 1332257 Emc4 ER membrane protein complex subunit 4 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20170105 MGI 1332257 Emc4 ER membrane protein complex subunit 4 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1332257 Emc4 ER membrane protein complex subunit 4 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1332257 Emc4 ER membrane protein complex subunit 4 gene MP:0010580 decreased heart left ventricle size IEA N RGD:5509061 20211021 MGI 1332257 Emc4 ER membrane protein complex subunit 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332257 Emc4 ER membrane protein complex subunit 4 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1332258 Wrnip1 Werner helicase interacting protein 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1332258 Wrnip1 Werner helicase interacting protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20201022 MGI 1332258 Wrnip1 Werner helicase interacting protein 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20190502 MGI 1332258 Wrnip1 Werner helicase interacting protein 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1332258 Wrnip1 Werner helicase interacting protein 1 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1332258 Wrnip1 Werner helicase interacting protein 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1332258 Wrnip1 Werner helicase interacting protein 1 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20160804 MGI 1332258 Wrnip1 Werner helicase interacting protein 1 gene MP:0005316 abnormal response to tactile stimuli IEA N RGD:5509061 20160804 MGI 1332258 Wrnip1 Werner helicase interacting protein 1 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20190502 MGI 1332258 Wrnip1 Werner helicase interacting protein 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20200402 MGI 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:19706529 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0004420 parietal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19706529 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:19706529 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0004459 small alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:19706529 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20171116 MGI PMID:19706529 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20141003 MGI PMID:19706529 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19706529 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:19706529 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20141003 MGI PMID:19706529 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19706529 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:19706529 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:19706529 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20141003 MGI PMID:19706529 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19706529 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0011942 decreased fluid intake IEA N RGD:5509061 20211021 MGI 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20201022 MGI 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0030353 wide sagittal suture IAGP N RGD:5509061 20171116 MGI PMID:19706529 1332260 Bnc2 basonuclin zinc finger protein 2 gene MP:0030387 large posterior fontanelle IAGP N RGD:5509061 20171207 MGI PMID:19706529 1332263 Gcgr glucagon receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20200310 MGI PMID:23160527 1332263 Gcgr glucagon receptor gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20200310 MGI PMID:28591637 1332263 Gcgr glucagon receptor gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20231207 MGI 1332263 Gcgr glucagon receptor gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20210429 MGI PMID:32677665 1332263 Gcgr glucagon receptor gene MP:0001261 obese IAGP N RGD:5509061 20200310 MGI PMID:25157166 1332263 Gcgr glucagon receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:25157166 1332263 Gcgr glucagon receptor gene MP:0001488 increased startle reflex IEA N RGD:5509061 20231207 MGI 1332263 Gcgr glucagon receptor gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1332263 Gcgr glucagon receptor gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1332263 Gcgr glucagon receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200310 MGI PMID:23160527 1332263 Gcgr glucagon receptor gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200310 MGI 1332263 Gcgr glucagon receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:10621976 1332263 Gcgr glucagon receptor gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1332263 Gcgr glucagon receptor gene MP:0002710 increased glucagon secretion IAGP N RGD:5509061 20200310 MGI PMID:23160527 1332263 Gcgr glucagon receptor gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20200310 MGI PMID:11785978 1332263 Gcgr glucagon receptor gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20200310 MGI PMID:23160527 1332263 Gcgr glucagon receptor gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20200310 MGI PMID:28591637 1332263 Gcgr glucagon receptor gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20210429 MGI PMID:32677665 1332263 Gcgr glucagon receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:23160527 1332263 Gcgr glucagon receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:28591637 1332263 Gcgr glucagon receptor gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200310 MGI PMID:23160527 1332263 Gcgr glucagon receptor gene MP:0002981 increased liver weight IAGP N RGD:5509061 20210429 MGI PMID:32677665 1332263 Gcgr glucagon receptor gene MP:0003068 enlarged kidney IEA N RGD:5509061 20200310 MGI 1332263 Gcgr glucagon receptor gene MP:0003365 increased glucagonoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 1332263 Gcgr glucagon receptor gene MP:0003917 increased kidney weight IEA N RGD:5509061 20210128 MGI 1332263 Gcgr glucagon receptor gene MP:0003960 increased lean body mass IEA N RGD:5509061 20231207 MGI 1332263 Gcgr glucagon receptor gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20200310 MGI PMID:23160527 1332263 Gcgr glucagon receptor gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 1332263 Gcgr glucagon receptor gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20200310 MGI PMID:28591637 1332263 Gcgr glucagon receptor gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20210429 MGI PMID:32677665 1332263 Gcgr glucagon receptor gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:25157166 1332263 Gcgr glucagon receptor gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:23160527 1332263 Gcgr glucagon receptor gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20210429 MGI PMID:32677665 1332263 Gcgr glucagon receptor gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20200310 MGI PMID:28591637 1332263 Gcgr glucagon receptor gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:28591637 1332263 Gcgr glucagon receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:23160527 1332263 Gcgr glucagon receptor gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 1332263 Gcgr glucagon receptor gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20231207 MGI 1332263 Gcgr glucagon receptor gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:25157166 1332263 Gcgr glucagon receptor gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0006087 increased body mass index IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20200310 MGI PMID:25157166 1332263 Gcgr glucagon receptor gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20200310 MGI PMID:23160527 1332263 Gcgr glucagon receptor gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20210429 MGI PMID:32677665 1332263 Gcgr glucagon receptor gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20200310 MGI PMID:23160527 1332263 Gcgr glucagon receptor gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20200310 MGI PMID:23160527 1332263 Gcgr glucagon receptor gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20200310 MGI PMID:28591637 1332263 Gcgr glucagon receptor gene MP:0009179 abnormal pancreatic alpha cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:25157166 1332263 Gcgr glucagon receptor gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1332263 Gcgr glucagon receptor gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12552113 1332263 Gcgr glucagon receptor gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0011940 decreased food intake IAGP N RGD:5509061 20200310 MGI PMID:25157166 1332263 Gcgr glucagon receptor gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:31230984 1332263 Gcgr glucagon receptor gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20210429 MGI PMID:32677665 1332263 Gcgr glucagon receptor gene MP:0013558 abnormal exocrine gland morphology IAGP N RGD:5509061 20200310 MGI PMID:21853126 1332263 Gcgr glucagon receptor gene MP:0014109 increased pancreatic alpha cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:23160527 1332263 Gcgr glucagon receptor gene MP:0014109 increased pancreatic alpha cell proliferation IAGP N RGD:5509061 20210429 MGI PMID:32677665 1332263 Gcgr glucagon receptor gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20210429 MGI PMID:32677665 1332263 Gcgr glucagon receptor gene MP:0020090 decreased susceptibility to diet-induced non-insulin dependent diabetes IAGP N RGD:5509061 20200310 MGI PMID:25157166 1332263 Gcgr glucagon receptor gene MP:0030589 increased pancreatic alpha cell mass IAGP N RGD:5509061 20200310 MGI PMID:23160527 1332263 Gcgr glucagon receptor gene MP:0031270 decreased susceptibility to age-related hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:21853126 1332267 Ift43 intraflagellar transport 43 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1332267 Ift43 intraflagellar transport 43 gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20181227 MGI 1332267 Ift43 intraflagellar transport 43 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20181227 MGI 1332267 Ift43 intraflagellar transport 43 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20181227 MGI 1332267 Ift43 intraflagellar transport 43 gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20181227 MGI 1332267 Ift43 intraflagellar transport 43 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1332267 Ift43 intraflagellar transport 43 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20181227 MGI 1332267 Ift43 intraflagellar transport 43 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20181227 MGI 1332267 Ift43 intraflagellar transport 43 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20181227 MGI 1332267 Ift43 intraflagellar transport 43 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1332267 Ift43 intraflagellar transport 43 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1332267 Ift43 intraflagellar transport 43 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1332267 Ift43 intraflagellar transport 43 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 1332267 Ift43 intraflagellar transport 43 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20181227 MGI 1332267 Ift43 intraflagellar transport 43 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332267 Ift43 intraflagellar transport 43 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1332268 Pfdn6 prefoldin subunit 6 gene MP:0001523 impaired righting response IEA N RGD:5509061 20170105 MGI 1332268 Pfdn6 prefoldin subunit 6 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1332268 Pfdn6 prefoldin subunit 6 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210826 MGI 1332268 Pfdn6 prefoldin subunit 6 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1332268 Pfdn6 prefoldin subunit 6 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332270 Tbck TBC1 domain containing kinase gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20240229 MGI PMID:37353954 1332270 Tbck TBC1 domain containing kinase gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20240229 MGI PMID:37353954 1332270 Tbck TBC1 domain containing kinase gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20240229 MGI PMID:37353954 1332270 Tbck TBC1 domain containing kinase gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20240229 MGI PMID:37353954 1332270 Tbck TBC1 domain containing kinase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0002959 increased urine microalbumin level IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0009552 urinary bladder obstruction IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0009646 urinary bladder inflammation IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332271 Gstk1 glutathione S-transferase kappa 1 gene MP:0011763 urethritis IAGP N RGD:5509061 20141003 MGI PMID:21826057 1332274 Kmt5a lysine methyltransferase 5A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19223465 1332274 Kmt5a lysine methyltransferase 5A gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:19223465 1332274 Kmt5a lysine methyltransferase 5A gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:19223465 1332274 Kmt5a lysine methyltransferase 5A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19223465 1332274 Kmt5a lysine methyltransferase 5A gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19223465 1332274 Kmt5a lysine methyltransferase 5A gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:19223465 1332274 Kmt5a lysine methyltransferase 5A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18319261 1332274 Kmt5a lysine methyltransferase 5A gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19223465 1332274 Kmt5a lysine methyltransferase 5A gene MP:0021086 decreased DNA replication IAGP N RGD:5509061 20220310 MGI PMID:19223465 1332275 Mphosph8 M-phase phosphoprotein 8 gene MP:0000440 domed cranium IAGP N RGD:5509061 20230126 MGI PMID:36332029 1332275 Mphosph8 M-phase phosphoprotein 8 gene MP:0000899 abnormal corpora quadrigemina morphology IAGP N RGD:5509061 20230126 MGI PMID:36332029 1332275 Mphosph8 M-phase phosphoprotein 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230126 MGI PMID:36332029 1332275 Mphosph8 M-phase phosphoprotein 8 gene MP:0002083 premature death IAGP N RGD:5509061 20230126 MGI PMID:36332029 1332275 Mphosph8 M-phase phosphoprotein 8 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20221103 MGI 1332275 Mphosph8 M-phase phosphoprotein 8 gene MP:0005238 increased brain size IAGP N RGD:5509061 20230126 MGI PMID:36332029 1332275 Mphosph8 M-phase phosphoprotein 8 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20230126 MGI PMID:36332029 1332275 Mphosph8 M-phase phosphoprotein 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20221103 MGI 1332275 Mphosph8 M-phase phosphoprotein 8 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20230601 MGI 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20200310 MGI PMID:19164486 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20200310 MGI PMID:24993824 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20200310 MGI PMID:24993824 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:24993824 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:24993824 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0004357 long tibia IEA N RGD:5509061 20200310 MGI 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20200310 MGI PMID:24993824 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20200310 MGI PMID:24993824 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:24993824 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20200310 MGI PMID:24993824 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20200310 MGI PMID:24993824 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0009854 impaired gastric peristalsis IAGP N RGD:5509061 20200310 MGI PMID:24993824 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20200310 MGI PMID:24993824 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20200310 MGI PMID:24993824 1332276 P2ry14 purinergic receptor P2Y, G-protein coupled, 14 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17242209 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:17242209 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17242209 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:17242209 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:17242209 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17242209 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:17242209 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:17242209 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0008902 abnormal renal fat pad morphology IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17242209 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332277 Trp53inp1 transformation related protein 53 inducible nuclear protein 1 gene MP:0020089 increased susceptibility to diet-induced non-insulin dependent diabetes IAGP N RGD:5509061 20170427 MGI PMID:25828351 1332278 Enoph1 enolase-phosphatase 1 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20231109 MGI PMID:37075968 1332278 Enoph1 enolase-phosphatase 1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20231109 MGI PMID:37075968 1332280 Aftph aftiphilin gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20230601 MGI 1332280 Aftph aftiphilin gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1332280 Aftph aftiphilin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210520 MGI 1332281 Ints10 integrator complex subunit 10 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1332281 Ints10 integrator complex subunit 10 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1332281 Ints10 integrator complex subunit 10 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1332281 Ints10 integrator complex subunit 10 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20181227 MGI 1332281 Ints10 integrator complex subunit 10 gene MP:0002824 abnormal chorioallantoic fusion IEA N RGD:5509061 20181227 MGI 1332281 Ints10 integrator complex subunit 10 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20181227 MGI 1332281 Ints10 integrator complex subunit 10 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1332281 Ints10 integrator complex subunit 10 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210826 MGI 1332281 Ints10 integrator complex subunit 10 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20181227 MGI 1332281 Ints10 integrator complex subunit 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332281 Ints10 integrator complex subunit 10 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210520 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20181227 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210520 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210520 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20181227 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20201022 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0002637 small uterus IEA N RGD:5509061 20210520 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20210520 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20181227 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0005313 absent adrenal gland IEA N RGD:5509061 20210520 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20240523 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20181227 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20181227 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1332284 Adnp2 ADNP homeobox 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 1332286 Tmem218 transmembrane protein 218 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20160114 MGI PMID:25161209 1332286 Tmem218 transmembrane protein 218 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20160114 MGI PMID:25161209 1332286 Tmem218 transmembrane protein 218 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160114 MGI PMID:25161209 1332286 Tmem218 transmembrane protein 218 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20160114 MGI PMID:25161209 1332286 Tmem218 transmembrane protein 218 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20160114 MGI PMID:25161209 1332286 Tmem218 transmembrane protein 218 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20160114 MGI PMID:25161209 1332286 Tmem218 transmembrane protein 218 gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20160114 MGI PMID:25161209 1332286 Tmem218 transmembrane protein 218 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20160114 MGI PMID:25161209 1332286 Tmem218 transmembrane protein 218 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20160114 MGI PMID:25161209 1332286 Tmem218 transmembrane protein 218 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20160114 MGI PMID:25161209 1332286 Tmem218 transmembrane protein 218 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20160114 MGI PMID:25161209 1332286 Tmem218 transmembrane protein 218 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20160114 MGI PMID:25161209 1332286 Tmem218 transmembrane protein 218 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20160114 MGI PMID:25161209 1332286 Tmem218 transmembrane protein 218 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20160114 MGI PMID:25161209 1332286 Tmem218 transmembrane protein 218 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20160114 MGI PMID:25161209 1332286 Tmem218 transmembrane protein 218 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:25161209 1332288 Cip2a cell proliferation regulating inhibitor of protein phosphatase 2A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22461891 1332288 Cip2a cell proliferation regulating inhibitor of protein phosphatase 2A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22461891 1332288 Cip2a cell proliferation regulating inhibitor of protein phosphatase 2A gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:22461891 1332288 Cip2a cell proliferation regulating inhibitor of protein phosphatase 2A gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:22461891 1332289 Apln apelin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18200044 1332289 Apln apelin gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:18200044 1332289 Apln apelin gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:18200044 1332289 Apln apelin gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:19767528 1332289 Apln apelin gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:17673668 1332289 Apln apelin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19767528 1332289 Apln apelin gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19767528 1332289 Apln apelin gene MP:0005412 vascular stenosis IAGP N RGD:5509061 20141003 MGI PMID:18200044 1332289 Apln apelin gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:19767528 1332289 Apln apelin gene MP:0020329 decreased capillary density IAGP N RGD:5509061 20160714 MGI PMID:18200044 1332289 Apln apelin gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:17673668 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0000155 asymmetric rib joints IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0000346 broad head IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20171207 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17639082 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20220519 MGI 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0004444 small supraoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0004445 small exoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0004472 broad nasal bone IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20230601 MGI 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17639082 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0008901 absent epididymal fat pad IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0030066 short face IAGP N RGD:5509061 20171207 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0030069 broad face IAGP N RGD:5509061 20171207 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0030288 broad occipital bone IAGP N RGD:5509061 20171102 MGI PMID:16980622 1332291 Psip1 PC4 and SFRS1 interacting protein 1 gene MP:0030289 flat occipital bone IAGP N RGD:5509061 20171102 MGI PMID:16980622 1332292 Prag1 PEAK1 related kinase activating pseudokinase 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1332292 Prag1 PEAK1 related kinase activating pseudokinase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160616 MGI PMID:25038227 1332292 Prag1 PEAK1 related kinase activating pseudokinase 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1332293 Aco2 aconitase 2, mitochondrial gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1332295 Exoc6 exocyst complex component 6 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:16289749 1332295 Exoc6 exocyst complex component 6 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:9292544 1332295 Exoc6 exocyst complex component 6 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20200310 MGI PMID:9292544 1332295 Exoc6 exocyst complex component 6 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20200310 MGI PMID:4596202 1332295 Exoc6 exocyst complex component 6 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:3960859 1332295 Exoc6 exocyst complex component 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1332295 Exoc6 exocyst complex component 6 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1332295 Exoc6 exocyst complex component 6 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20200310 MGI PMID:4596202 1332295 Exoc6 exocyst complex component 6 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:16289749 1332295 Exoc6 exocyst complex component 6 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20200310 MGI PMID:4596202 1332295 Exoc6 exocyst complex component 6 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20200310 MGI PMID:16289749 1332295 Exoc6 exocyst complex component 6 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20200310 MGI PMID:9292544 1332295 Exoc6 exocyst complex component 6 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20200310 MGI PMID:3960859 1332295 Exoc6 exocyst complex component 6 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20200310 MGI PMID:3960859 1332295 Exoc6 exocyst complex component 6 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20200310 MGI PMID:3960859 1332295 Exoc6 exocyst complex component 6 gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20200310 MGI PMID:16289749 1332295 Exoc6 exocyst complex component 6 gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20200310 MGI PMID:3960859 1332295 Exoc6 exocyst complex component 6 gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20200310 MGI PMID:9292544 1332295 Exoc6 exocyst complex component 6 gene MP:0002813 microcytosis IAGP N RGD:5509061 20200310 MGI PMID:3960859 1332295 Exoc6 exocyst complex component 6 gene MP:0002813 microcytosis IAGP N RGD:5509061 20200310 MGI PMID:9292544 1332295 Exoc6 exocyst complex component 6 gene MP:0002814 hyperchromasia IAGP N RGD:5509061 20200310 MGI PMID:4596202 1332295 Exoc6 exocyst complex component 6 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:16289749 1332295 Exoc6 exocyst complex component 6 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:3960859 1332295 Exoc6 exocyst complex component 6 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:9292544 1332295 Exoc6 exocyst complex component 6 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:4596202 1332295 Exoc6 exocyst complex component 6 gene MP:0003717 pallor IEA N RGD:5509061 20200310 MGI 1332295 Exoc6 exocyst complex component 6 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20200310 MGI PMID:3960859 1332295 Exoc6 exocyst complex component 6 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20200310 MGI PMID:4596202 1332295 Exoc6 exocyst complex component 6 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20200310 MGI PMID:3960859 1332295 Exoc6 exocyst complex component 6 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20200310 MGI PMID:4596202 1332295 Exoc6 exocyst complex component 6 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200310 MGI PMID:3960859 1332295 Exoc6 exocyst complex component 6 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20200310 MGI PMID:16289749 1332295 Exoc6 exocyst complex component 6 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20200310 MGI PMID:9292544 1332295 Exoc6 exocyst complex component 6 gene MP:0008387 hypochromic anemia IAGP N RGD:5509061 20200310 MGI PMID:4596202 1332295 Exoc6 exocyst complex component 6 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20200310 MGI PMID:3960859 1332295 Exoc6 exocyst complex component 6 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20200310 MGI PMID:3960859 1332295 Exoc6 exocyst complex component 6 gene MP:0009931 abnormal skin appearance IEA N RGD:5509061 20200310 MGI 1332295 Exoc6 exocyst complex component 6 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:4596202 1332295 Exoc6 exocyst complex component 6 gene MP:0011188 increased erythrocyte protoporphyrin level IAGP N RGD:5509061 20200310 MGI PMID:3960859 1332295 Exoc6 exocyst complex component 6 gene MP:0011188 increased erythrocyte protoporphyrin level IAGP N RGD:5509061 20200310 MGI PMID:9292544 1332295 Exoc6 exocyst complex component 6 gene MP:0031084 decreased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:3960859 1332295 Exoc6 exocyst complex component 6 gene MP:0031084 decreased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:4596202 1332296 Mtdh metadherin gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:24981741 1332296 Mtdh metadherin gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20200310 MGI PMID:24981741 1332296 Mtdh metadherin gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:24981741 1332296 Mtdh metadherin gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:25193383 1332296 Mtdh metadherin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:25193383 1332296 Mtdh metadherin gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20200310 MGI PMID:24981741 1332296 Mtdh metadherin gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20200310 MGI PMID:25193383 1332296 Mtdh metadherin gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:25193383 1332296 Mtdh metadherin gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20200310 MGI PMID:25193383 1332296 Mtdh metadherin gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:24981741 1332296 Mtdh metadherin gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20200310 MGI PMID:24981741 1332296 Mtdh metadherin gene MP:0010266 decreased liver tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:25193383 1332296 Mtdh metadherin gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:25193383 1332296 Mtdh metadherin gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:24981741 1332296 Mtdh metadherin gene MP:0010282 decreased organ/body region tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:25193383 1332296 Mtdh metadherin gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20200310 MGI PMID:24981741 1332296 Mtdh metadherin gene MP:0011986 decreased macrophage proliferation IAGP N RGD:5509061 20200310 MGI PMID:25193383 1332296 Mtdh metadherin gene MP:0012419 decreased cardiovascular system tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:25193383 1332298 Pik3c2g phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma gene MP:0001260 increased body weight IAGP N RGD:5509061 20160714 MGI PMID:26100075 1332298 Pik3c2g phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20160714 MGI PMID:26100075 1332298 Pik3c2g phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160714 MGI PMID:26100075 1332298 Pik3c2g phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160714 MGI PMID:26100075 1332298 Pik3c2g phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20160714 MGI PMID:26100075 1332298 Pik3c2g phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20160714 MGI PMID:26100075 1332298 Pik3c2g phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20160714 MGI PMID:26100075 1332298 Pik3c2g phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma gene MP:0005331 insulin resistance IAGP N RGD:5509061 20160714 MGI PMID:26100075 1332298 Pik3c2g phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20160714 MGI PMID:26100075 1332298 Pik3c2g phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20160714 MGI PMID:26100075 1332298 Pik3c2g phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20160714 MGI PMID:26100075 1332298 Pik3c2g phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20160714 MGI PMID:26100075 1332298 Pik3c2g phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20160714 MGI PMID:26100075 1332300 Duox2 dual oxidase 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20220915 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 1332300 Duox2 dual oxidase 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20201022 MGI 1332300 Duox2 dual oxidase 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1332300 Duox2 dual oxidase 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20201022 MGI 1332300 Duox2 dual oxidase 2 gene MP:0000601 small liver IEA N RGD:5509061 20201022 MGI 1332300 Duox2 dual oxidase 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1332300 Duox2 dual oxidase 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1332300 Duox2 dual oxidase 2 gene MP:0000692 small spleen IEA N RGD:5509061 20201022 MGI 1332300 Duox2 dual oxidase 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1332300 Duox2 dual oxidase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210930 MGI PMID:33905568 1332300 Duox2 dual oxidase 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1332300 Duox2 dual oxidase 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1332300 Duox2 dual oxidase 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1332300 Duox2 dual oxidase 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1332300 Duox2 dual oxidase 2 gene MP:0002188 small heart IEA N RGD:5509061 20201022 MGI 1332300 Duox2 dual oxidase 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1332300 Duox2 dual oxidase 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 1332300 Duox2 dual oxidase 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 1332300 Duox2 dual oxidase 2 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20200514 MGI 1332300 Duox2 dual oxidase 2 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20200514 MGI 1332300 Duox2 dual oxidase 2 gene MP:0002989 small kidney IEA N RGD:5509061 20210128 MGI 1332300 Duox2 dual oxidase 2 gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 1332300 Duox2 dual oxidase 2 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0003402 decreased liver weight IEA N RGD:5509061 20220519 MGI 1332300 Duox2 dual oxidase 2 gene MP:0003498 thyroid gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0004664 delayed inner ear development IAGP N RGD:5509061 20141003 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0004692 small pubis IAGP N RGD:5509061 20210930 MGI PMID:33905568 1332300 Duox2 dual oxidase 2 gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 1332300 Duox2 dual oxidase 2 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1332300 Duox2 dual oxidase 2 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1332300 Duox2 dual oxidase 2 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 1332300 Duox2 dual oxidase 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200514 MGI 1332300 Duox2 dual oxidase 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1332300 Duox2 dual oxidase 2 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1332300 Duox2 dual oxidase 2 gene MP:0011721 abnormal bone mineralization involved in bone maturation IAGP N RGD:5509061 20150319 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1332300 Duox2 dual oxidase 2 gene MP:0013618 decreased areal bone mineral density IAGP N RGD:5509061 20150319 MGI PMID:17440044 1332300 Duox2 dual oxidase 2 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1332305 Insig1 insulin induced gene 1 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20210128 MGI 1332305 Insig1 insulin induced gene 1 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 1332305 Insig1 insulin induced gene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16100574 1332305 Insig1 insulin induced gene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:16100574 1332305 Insig1 insulin induced gene 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23919961 1332305 Insig1 insulin induced gene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23919961 1332305 Insig1 insulin induced gene 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210520 MGI 1332305 Insig1 insulin induced gene 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16100574 1332305 Insig1 insulin induced gene 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16100574 1332305 Insig1 insulin induced gene 1 gene MP:0002139 abnormal hepatobiliary system physiology IAGP N RGD:5509061 20141003 MGI PMID:16100574 1332305 Insig1 insulin induced gene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16100574 1332305 Insig1 insulin induced gene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23919961 1332305 Insig1 insulin induced gene 1 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20211021 MGI 1332305 Insig1 insulin induced gene 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16100574 1332305 Insig1 insulin induced gene 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16100574 1332305 Insig1 insulin induced gene 1 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16100574 1332305 Insig1 insulin induced gene 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1332305 Insig1 insulin induced gene 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 1332305 Insig1 insulin induced gene 1 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20240523 MGI 1332305 Insig1 insulin induced gene 1 gene MP:0005655 increased aggression IEA N RGD:5509061 20221215 MGI 1332305 Insig1 insulin induced gene 1 gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23919961 1332305 Insig1 insulin induced gene 1 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23919961 1332305 Insig1 insulin induced gene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16100574 1332305 Insig1 insulin induced gene 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16100574 1332305 Insig1 insulin induced gene 1 gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23919961 1332305 Insig1 insulin induced gene 1 gene MP:0011169 abnormal white fat cell differentation IAGP N RGD:5509061 20141003 MGI PMID:23919961 1332305 Insig1 insulin induced gene 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20231207 MGI 1332305 Insig1 insulin induced gene 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:18838740 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18838740 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:18838740 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0002764 short tibia IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0003900 shortened QT interval IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0010511 shortened PR interval IEA N RGD:5509061 20240523 MGI 1332308 Elovl5 ELOVL fatty acid elongase 5 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1332311 Gins4 GINS complex subunit 4 gene MP:0001297 microphthalmia IEA N RGD:5509061 20190502 MGI 1332311 Gins4 GINS complex subunit 4 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1332311 Gins4 GINS complex subunit 4 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1332311 Gins4 GINS complex subunit 4 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:24244394 1332311 Gins4 GINS complex subunit 4 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20211021 MGI 1332311 Gins4 GINS complex subunit 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24244394 1332311 Gins4 GINS complex subunit 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332311 Gins4 GINS complex subunit 4 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 1332311 Gins4 GINS complex subunit 4 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:24244394 1332311 Gins4 GINS complex subunit 4 gene MP:0012743 increased inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24244394 1332311 Gins4 GINS complex subunit 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:23529610 1332312 Xbp1 X-box binding protein 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10425189 1332312 Xbp1 X-box binding protein 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10425189 1332312 Xbp1 X-box binding protein 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:10425189 1332312 Xbp1 X-box binding protein 1 gene MP:0000296 absent trabeculae carneae IAGP N RGD:5509061 20141003 MGI PMID:10425189 1332312 Xbp1 X-box binding protein 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23529610 1332312 Xbp1 X-box binding protein 1 gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20141003 MGI PMID:18775308 1332312 Xbp1 X-box binding protein 1 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:18775308 1332312 Xbp1 X-box binding protein 1 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:10652269 1332312 Xbp1 X-box binding protein 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10652269 1332312 Xbp1 X-box binding protein 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:10652269 1332312 Xbp1 X-box binding protein 1 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:10425189 1332312 Xbp1 X-box binding protein 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210826 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10652269 1332312 Xbp1 X-box binding protein 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10652269 1332312 Xbp1 X-box binding protein 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23529610 1332312 Xbp1 X-box binding protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19805353 1332312 Xbp1 X-box binding protein 1 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:24089213 1332312 Xbp1 X-box binding protein 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18556558 1332312 Xbp1 X-box binding protein 1 gene MP:0002316 anoxia IAGP N RGD:5509061 20141003 MGI PMID:10425189 1332312 Xbp1 X-box binding protein 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18775308 1332312 Xbp1 X-box binding protein 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20170105 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18556558 1332312 Xbp1 X-box binding protein 1 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:18775308 1332312 Xbp1 X-box binding protein 1 gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18775308 1332312 Xbp1 X-box binding protein 1 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:18775308 1332312 Xbp1 X-box binding protein 1 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:24089213 1332312 Xbp1 X-box binding protein 1 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20190523 MGI PMID:30254094 1332312 Xbp1 X-box binding protein 1 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:23529610 1332312 Xbp1 X-box binding protein 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:10652269 1332312 Xbp1 X-box binding protein 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:23529610 1332312 Xbp1 X-box binding protein 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160804 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20191128 MGI PMID:29551634 1332312 Xbp1 X-box binding protein 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10652269 1332312 Xbp1 X-box binding protein 1 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18556558 1332312 Xbp1 X-box binding protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10425189 1332312 Xbp1 X-box binding protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10652269 1332312 Xbp1 X-box binding protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23529610 1332312 Xbp1 X-box binding protein 1 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:10652269 1332312 Xbp1 X-box binding protein 1 gene MP:0004264 abnormal extraembryonic tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:19805353 1332312 Xbp1 X-box binding protein 1 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20141003 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24089213 1332312 Xbp1 X-box binding protein 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20160804 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:18775308 1332312 Xbp1 X-box binding protein 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:23529610 1332312 Xbp1 X-box binding protein 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18556558 1332312 Xbp1 X-box binding protein 1 gene MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20141003 MGI PMID:18178615 1332312 Xbp1 X-box binding protein 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:23529610 1332312 Xbp1 X-box binding protein 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18775308 1332312 Xbp1 X-box binding protein 1 gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:10425189 1332312 Xbp1 X-box binding protein 1 gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20141003 MGI PMID:18775308 1332312 Xbp1 X-box binding protein 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:24089213 1332312 Xbp1 X-box binding protein 1 gene MP:0008495 decreased IgG1 level IEA N RGD:5509061 20160804 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:18775308 1332312 Xbp1 X-box binding protein 1 gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:24089213 1332312 Xbp1 X-box binding protein 1 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20190523 MGI PMID:30254094 1332312 Xbp1 X-box binding protein 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:18775308 1332312 Xbp1 X-box binding protein 1 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:23529610 1332312 Xbp1 X-box binding protein 1 gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20141003 MGI PMID:24089213 1332312 Xbp1 X-box binding protein 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20160804 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23529610 1332312 Xbp1 X-box binding protein 1 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:18775308 1332312 Xbp1 X-box binding protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10425189 1332312 Xbp1 X-box binding protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10652269 1332312 Xbp1 X-box binding protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23529610 1332312 Xbp1 X-box binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0012361 decreased large unstained cell number IEA N RGD:5509061 20211021 MGI 1332312 Xbp1 X-box binding protein 1 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:10425189 1332312 Xbp1 X-box binding protein 1 gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20150312 MGI PMID:18775308 1332312 Xbp1 X-box binding protein 1 gene MP:0013792 abnormal small intestine goblet cell morphology IAGP N RGD:5509061 20160310 MGI PMID:18775308 1332312 Xbp1 X-box binding protein 1 gene MP:0014076 absent Paneth cells IAGP N RGD:5509061 20160310 MGI PMID:18775308 1332312 Xbp1 X-box binding protein 1 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20191128 MGI PMID:29551634 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200917 MGI PMID:31183559 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20211118 MGI PMID:27875292 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20211118 MGI PMID:27875292 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20200917 MGI PMID:31183559 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20200917 MGI PMID:31183559 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20200917 MGI PMID:31183559 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20211118 MGI PMID:27875292 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20211118 MGI PMID:27875292 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20200917 MGI PMID:31183559 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20200917 MGI PMID:31183559 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20200917 MGI PMID:31183559 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20211118 MGI PMID:27875292 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20200917 MGI PMID:31183559 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20211118 MGI PMID:27875292 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20200917 MGI PMID:31183559 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20211118 MGI PMID:27875292 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20211118 MGI PMID:27875292 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:31183559 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0011987 abnormal GABAergic neuron physiology IAGP N RGD:5509061 20211118 MGI PMID:27875292 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:27875292 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:31183559 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0014384 increased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:31183559 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:27875292 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0020358 abnormal inhibitory synapse morphology IAGP N RGD:5509061 20211118 MGI PMID:27875292 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0020870 decreased thigmotaxis IAGP N RGD:5509061 20200917 MGI PMID:31183559 1332314 Zdhhc7 zinc finger, DHHC domain containing 7 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:31183559 1332315 Hibadh 3-hydroxyisobutyrate dehydrogenase gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1332315 Hibadh 3-hydroxyisobutyrate dehydrogenase gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1332315 Hibadh 3-hydroxyisobutyrate dehydrogenase gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1332315 Hibadh 3-hydroxyisobutyrate dehydrogenase gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 1332315 Hibadh 3-hydroxyisobutyrate dehydrogenase gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1332315 Hibadh 3-hydroxyisobutyrate dehydrogenase gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0000111 cleft palate IEA N RGD:5509061 20210520 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20210520 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20220519 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20210520 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210520 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20210826 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20210520 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210520 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210826 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20210520 MGI 1332316 Fgfr1op2 FGFR1 oncogene partner 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:23467409 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:23467409 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161013 MGI PMID:26512886 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20161013 MGI PMID:26512886 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20161013 MGI PMID:26512886 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23467409 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:23467409 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20161013 MGI PMID:26512886 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23467409 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23467409 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23467409 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23467409 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20161013 MGI PMID:26512886 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20161013 MGI PMID:26512886 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0005655 increased aggression IEA N RGD:5509061 20201231 MGI 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20161013 MGI PMID:26512886 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20161013 MGI PMID:26512886 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23467409 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20161013 MGI PMID:26512886 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20161013 MGI PMID:26512886 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23467409 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23467409 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23467409 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0011169 abnormal white fat cell differentation IAGP N RGD:5509061 20161013 MGI PMID:26512886 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:23467409 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0011702 abnormal fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:23467409 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:23467409 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20161013 MGI PMID:26512886 1332317 Arhgef11 Rho guanine nucleotide exchange factor 11 gene MP:0020090 decreased susceptibility to diet-induced non-insulin dependent diabetes IAGP N RGD:5509061 20161013 MGI PMID:26512886 1332318 Cpxm2 carboxypeptidase X, M14 family member 2 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20240307 MGI PMID:34916661 1332318 Cpxm2 carboxypeptidase X, M14 family member 2 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20240307 MGI PMID:34916661 1332318 Cpxm2 carboxypeptidase X, M14 family member 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20240307 MGI PMID:34916661 1332318 Cpxm2 carboxypeptidase X, M14 family member 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20240307 MGI PMID:34916661 1332318 Cpxm2 carboxypeptidase X, M14 family member 2 gene MP:0020204 abnormal heart left ventricle weight IAGP N RGD:5509061 20240307 MGI PMID:34916661 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:23792766 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:23792766 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220519 MGI 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20201022 MGI 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:21553379 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:21553379 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:23792766 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0000601 small liver IEA N RGD:5509061 20210128 MGI 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:23792766 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210826 MGI 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0002728 absent tibia IAGP N RGD:5509061 20141003 MGI PMID:23792766 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:21553379 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:23792766 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:21553379 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0002989 small kidney IEA N RGD:5509061 20210128 MGI 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23792766 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20210128 MGI 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:23792766 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:21553379 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:21553379 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0004540 small maxilla IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:23792766 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0005430 absent fibula IAGP N RGD:5509061 20141003 MGI PMID:23792766 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0005576 decreased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20230601 MGI 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0008160 increased diameter of humerus IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0008161 increased diameter of radius IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0008163 increased diameter of ulna IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:21553379 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:23792766 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:23792766 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19097194 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23792766 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0011495 abnormal head shape IEA N RGD:5509061 20201022 MGI 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0014106 delayed chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:19465597 1332319 Pkdcc protein kinase domain containing, cytoplasmic gene MP:0021208 median cleft palate IAGP N RGD:5509061 20221201 MGI PMID:19097194 1332320 Inpp5j inositol polyphosphate 5-phosphatase J gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20170314 MGI PMID:26267533 1332320 Inpp5j inositol polyphosphate 5-phosphatase J gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1332320 Inpp5j inositol polyphosphate 5-phosphatase J gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1332320 Inpp5j inositol polyphosphate 5-phosphatase J gene MP:0001200 thick skin IEA N RGD:5509061 20230601 MGI 1332320 Inpp5j inositol polyphosphate 5-phosphatase J gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20170314 MGI PMID:26267533 1332320 Inpp5j inositol polyphosphate 5-phosphatase J gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1332320 Inpp5j inositol polyphosphate 5-phosphatase J gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1332320 Inpp5j inositol polyphosphate 5-phosphatase J gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170314 MGI PMID:26267533 1332320 Inpp5j inositol polyphosphate 5-phosphatase J gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20170314 MGI PMID:26267533 1332320 Inpp5j inositol polyphosphate 5-phosphatase J gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20170314 MGI PMID:26267533 1332320 Inpp5j inositol polyphosphate 5-phosphatase J gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20170314 MGI PMID:26267533 1332320 Inpp5j inositol polyphosphate 5-phosphatase J gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20170314 MGI PMID:26267533 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20190502 MGI 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000553 absent radius IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20160218 MGI PMID:26531099 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20160218 MGI PMID:26531099 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20160218 MGI PMID:26531099 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000614 absent salivary gland IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20190502 MGI 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0001181 absent lungs IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0001196 shiny skin IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0001199 thin skin IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0003853 dry skin IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20160218 MGI PMID:26531099 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0004197 abnormal fetal growth/weight/body size IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0004352 absent humerus IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20160218 MGI PMID:26531099 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20160218 MGI PMID:26531099 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0009893 cleft primary palate IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0013545 cleft hard palate IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0013546 cleft soft palate IAGP N RGD:5509061 20160218 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:26371508 1332322 Esrp2 epithelial splicing regulatory protein 2 gene MP:0031504 increased mouth width IAGP N RGD:5509061 20230810 MGI PMID:26371508 1332323 Srd5a3 steroid 5 alpha-reductase 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:20637498 1332323 Srd5a3 steroid 5 alpha-reductase 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1332323 Srd5a3 steroid 5 alpha-reductase 3 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20160811 MGI 1332323 Srd5a3 steroid 5 alpha-reductase 3 gene MP:0002861 abnormal tail bud morphology IEA N RGD:5509061 20160811 MGI 1332323 Srd5a3 steroid 5 alpha-reductase 3 gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:20637498 1332323 Srd5a3 steroid 5 alpha-reductase 3 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1332323 Srd5a3 steroid 5 alpha-reductase 3 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:20637498 1332323 Srd5a3 steroid 5 alpha-reductase 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1332323 Srd5a3 steroid 5 alpha-reductase 3 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:20637498 1332323 Srd5a3 steroid 5 alpha-reductase 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20637498 1332323 Srd5a3 steroid 5 alpha-reductase 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1332323 Srd5a3 steroid 5 alpha-reductase 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1332324 Prap1 proline-rich acidic protein 1 gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20200310 MGI 1332324 Prap1 proline-rich acidic protein 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20210506 MGI PMID:32629119 1332324 Prap1 proline-rich acidic protein 1 gene MP:0002461 increased immunoglobulin level IEA N RGD:5509061 20200310 MGI 1332324 Prap1 proline-rich acidic protein 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20210506 MGI PMID:32629119 1332324 Prap1 proline-rich acidic protein 1 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20210506 MGI PMID:32629119 1332324 Prap1 proline-rich acidic protein 1 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20210506 MGI PMID:32629119 1332324 Prap1 proline-rich acidic protein 1 gene MP:0008599 increased circulating interleukin-2 level IAGP N RGD:5509061 20210506 MGI PMID:32629119 1332324 Prap1 proline-rich acidic protein 1 gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20210506 MGI PMID:32629119 1332324 Prap1 proline-rich acidic protein 1 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20210506 MGI PMID:32629119 1332324 Prap1 proline-rich acidic protein 1 gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20210506 MGI PMID:32629119 1332324 Prap1 proline-rich acidic protein 1 gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20210506 MGI PMID:32629119 1332324 Prap1 proline-rich acidic protein 1 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20210506 MGI PMID:32629119 1332324 Prap1 proline-rich acidic protein 1 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20210506 MGI PMID:32629119 1332324 Prap1 proline-rich acidic protein 1 gene MP:0012734 abnormal response to radiation IAGP N RGD:5509061 20210506 MGI PMID:32629119 1332327 Mettl22 methyltransferase 22, Kin17 lysine gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1332327 Mettl22 methyltransferase 22, Kin17 lysine gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1332328 Tmem163 transmembrane protein 163 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1332328 Tmem163 transmembrane protein 163 gene MP:0000088 short mandible IAGP N RGD:5509061 20170525 MGI PMID:11316774 1332328 Tmem163 transmembrane protein 163 gene MP:0000088 short mandible IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20170525 MGI PMID:21303853 1332328 Tmem163 transmembrane protein 163 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20170525 MGI PMID:22560297 1332328 Tmem163 transmembrane protein 163 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20170525 MGI PMID:21303853 1332328 Tmem163 transmembrane protein 163 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20170525 MGI PMID:22560297 1332328 Tmem163 transmembrane protein 163 gene MP:0000154 rib fusion IAGP N RGD:5509061 20170525 MGI PMID:22560297 1332328 Tmem163 transmembrane protein 163 gene MP:0000160 kyphosis IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20170525 MGI PMID:21303853 1332328 Tmem163 transmembrane protein 163 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20170525 MGI PMID:21303853 1332328 Tmem163 transmembrane protein 163 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20231109 MGI PMID:34050709 1332328 Tmem163 transmembrane protein 163 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231109 MGI PMID:34050709 1332328 Tmem163 transmembrane protein 163 gene MP:0000373 belly spot IAGP N RGD:5509061 20170525 MGI PMID:24247431 1332328 Tmem163 transmembrane protein 163 gene MP:0000440 domed cranium IAGP N RGD:5509061 20170525 MGI PMID:11316774 1332328 Tmem163 transmembrane protein 163 gene MP:0000445 short snout IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0000585 kinked tail IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20170525 MGI PMID:14676301 1332328 Tmem163 transmembrane protein 163 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20170525 MGI PMID:14676301 1332328 Tmem163 transmembrane protein 163 gene MP:0000690 absent spleen IAGP N RGD:5509061 20170525 MGI PMID:22560297 1332328 Tmem163 transmembrane protein 163 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20170525 MGI PMID:14676301 1332328 Tmem163 transmembrane protein 163 gene MP:0000745 tremors IAGP N RGD:5509061 20170525 MGI PMID:24589777 1332328 Tmem163 transmembrane protein 163 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20170525 MGI PMID:15975937 1332328 Tmem163 transmembrane protein 163 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20170525 MGI PMID:18202285 1332328 Tmem163 transmembrane protein 163 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20170525 MGI PMID:21303853 1332328 Tmem163 transmembrane protein 163 gene MP:0000914 exencephaly IAGP N RGD:5509061 20170525 MGI PMID:17360769 1332328 Tmem163 transmembrane protein 163 gene MP:0000929 open neural tube IAGP N RGD:5509061 20170525 MGI PMID:15975937 1332328 Tmem163 transmembrane protein 163 gene MP:0000929 open neural tube IAGP N RGD:5509061 20170525 MGI PMID:21303853 1332328 Tmem163 transmembrane protein 163 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20170525 MGI PMID:18202285 1332328 Tmem163 transmembrane protein 163 gene MP:0001017 abnormal stellate ganglion morphology IAGP N RGD:5509061 20201217 MGI PMID:31218818 1332328 Tmem163 transmembrane protein 163 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20170525 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20170525 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20220721 MGI PMID:34977916 1332328 Tmem163 transmembrane protein 163 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20170525 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20170525 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20170525 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20170525 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0001147 small testis IAGP N RGD:5509061 20170525 MGI PMID:17142319 1332328 Tmem163 transmembrane protein 163 gene MP:0001147 small testis IAGP N RGD:5509061 20170525 MGI PMID:18755802 1332328 Tmem163 transmembrane protein 163 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20170525 MGI PMID:17142319 1332328 Tmem163 transmembrane protein 163 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20170525 MGI PMID:17142319 1332328 Tmem163 transmembrane protein 163 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20170525 MGI PMID:18755802 1332328 Tmem163 transmembrane protein 163 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0001159 absent prostate gland IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0001261 obese IAGP N RGD:5509061 20170525 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180607 MGI PMID:29222403 1332328 Tmem163 transmembrane protein 163 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170525 MGI PMID:12724423 1332328 Tmem163 transmembrane protein 163 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170525 MGI PMID:16287843 1332328 Tmem163 transmembrane protein 163 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170525 MGI PMID:24247431 1332328 Tmem163 transmembrane protein 163 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170525 MGI PMID:24589777 1332328 Tmem163 transmembrane protein 163 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170525 MGI PMID:27053202 1332328 Tmem163 transmembrane protein 163 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20170525 MGI PMID:11316774 1332328 Tmem163 transmembrane protein 163 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0001304 cataract IAGP N RGD:5509061 20170525 MGI PMID:17470285 1332328 Tmem163 transmembrane protein 163 gene MP:0001304 cataract IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20170525 MGI PMID:19679071 1332328 Tmem163 transmembrane protein 163 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20180607 MGI PMID:29222403 1332328 Tmem163 transmembrane protein 163 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20170525 MGI PMID:14676301 1332328 Tmem163 transmembrane protein 163 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20170525 MGI PMID:22697126 1332328 Tmem163 transmembrane protein 163 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20170525 MGI PMID:19679071 1332328 Tmem163 transmembrane protein 163 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20180607 MGI PMID:29222403 1332328 Tmem163 transmembrane protein 163 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20170525 MGI PMID:24589777 1332328 Tmem163 transmembrane protein 163 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20170525 MGI PMID:21303853 1332328 Tmem163 transmembrane protein 163 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170525 MGI PMID:12724423 1332328 Tmem163 transmembrane protein 163 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20170525 MGI PMID:14676301 1332328 Tmem163 transmembrane protein 163 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20170525 MGI PMID:24589777 1332328 Tmem163 transmembrane protein 163 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20170525 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0001925 male infertility IAGP N RGD:5509061 20170525 MGI PMID:18316482 1332328 Tmem163 transmembrane protein 163 gene MP:0001925 male infertility IAGP N RGD:5509061 20170525 MGI PMID:18755802 1332328 Tmem163 transmembrane protein 163 gene MP:0001926 female infertility IAGP N RGD:5509061 20170525 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0001926 female infertility IAGP N RGD:5509061 20220721 MGI PMID:34977916 1332328 Tmem163 transmembrane protein 163 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20170525 MGI PMID:18316482 1332328 Tmem163 transmembrane protein 163 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20170525 MGI PMID:27053202 1332328 Tmem163 transmembrane protein 163 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20170525 MGI PMID:11316774 1332328 Tmem163 transmembrane protein 163 gene MP:0001956 hypopnea IAGP N RGD:5509061 20170525 MGI PMID:27053202 1332328 Tmem163 transmembrane protein 163 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20170525 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1332328 Tmem163 transmembrane protein 163 gene MP:0002064 seizures IAGP N RGD:5509061 20170525 MGI PMID:24589777 1332328 Tmem163 transmembrane protein 163 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20231207 MGI 1332328 Tmem163 transmembrane protein 163 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20170525 MGI PMID:19679071 1332328 Tmem163 transmembrane protein 163 gene MP:0002083 premature death IAGP N RGD:5509061 20170525 MGI PMID:24589777 1332328 Tmem163 transmembrane protein 163 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20170525 MGI PMID:21303853 1332328 Tmem163 transmembrane protein 163 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1332328 Tmem163 transmembrane protein 163 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20170525 MGI PMID:21303853 1332328 Tmem163 transmembrane protein 163 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170525 MGI PMID:14657014 1332328 Tmem163 transmembrane protein 163 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20170525 MGI PMID:17142319 1332328 Tmem163 transmembrane protein 163 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20170525 MGI PMID:17142319 1332328 Tmem163 transmembrane protein 163 gene MP:0002669 abnormal scrotum morphology IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20170525 MGI PMID:18755802 1332328 Tmem163 transmembrane protein 163 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20170525 MGI PMID:17470285 1332328 Tmem163 transmembrane protein 163 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20170525 MGI PMID:17142319 1332328 Tmem163 transmembrane protein 163 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20170525 MGI PMID:18755802 1332328 Tmem163 transmembrane protein 163 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20170525 MGI PMID:17142319 1332328 Tmem163 transmembrane protein 163 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1332328 Tmem163 transmembrane protein 163 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20180607 MGI PMID:29222403 1332328 Tmem163 transmembrane protein 163 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20170525 MGI PMID:11316774 1332328 Tmem163 transmembrane protein 163 gene MP:0003124 hypospadia IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0003234 enhanced NMDA-mediated synaptic currents IAGP N RGD:5509061 20180607 MGI PMID:29222403 1332328 Tmem163 transmembrane protein 163 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20170525 MGI PMID:21303853 1332328 Tmem163 transmembrane protein 163 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20170525 MGI PMID:12724423 1332328 Tmem163 transmembrane protein 163 gene MP:0003417 premature endochondral bone ossification IAGP N RGD:5509061 20170525 MGI PMID:11316774 1332328 Tmem163 transmembrane protein 163 gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20170525 MGI PMID:18755802 1332328 Tmem163 transmembrane protein 163 gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20170525 MGI PMID:11316774 1332328 Tmem163 transmembrane protein 163 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20170525 MGI PMID:12724423 1332328 Tmem163 transmembrane protein 163 gene MP:0003718 maternal effect IAGP N RGD:5509061 20220120 MGI PMID:34931676 1332328 Tmem163 transmembrane protein 163 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 1332328 Tmem163 transmembrane protein 163 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20231207 MGI 1332328 Tmem163 transmembrane protein 163 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20170525 MGI PMID:16287843 1332328 Tmem163 transmembrane protein 163 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20170525 MGI PMID:22315402 1332328 Tmem163 transmembrane protein 163 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20170525 MGI PMID:22315402 1332328 Tmem163 transmembrane protein 163 gene MP:0004218 meiotic nondisjunction during M1 phase IAGP N RGD:5509061 20170525 MGI PMID:18316482 1332328 Tmem163 transmembrane protein 163 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0004344 scapular bone hypoplasia IAGP N RGD:5509061 20170525 MGI PMID:22560297 1332328 Tmem163 transmembrane protein 163 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20170525 MGI PMID:22560297 1332328 Tmem163 transmembrane protein 163 gene MP:0004672 short ribs IAGP N RGD:5509061 20170525 MGI PMID:22560297 1332328 Tmem163 transmembrane protein 163 gene MP:0004727 absent epididymis IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20170525 MGI PMID:11316774 1332328 Tmem163 transmembrane protein 163 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20170525 MGI PMID:18316482 1332328 Tmem163 transmembrane protein 163 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20170525 MGI PMID:18755802 1332328 Tmem163 transmembrane protein 163 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20170525 MGI PMID:14676301 1332328 Tmem163 transmembrane protein 163 gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20170525 MGI PMID:18755802 1332328 Tmem163 transmembrane protein 163 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20170525 MGI PMID:14676301 1332328 Tmem163 transmembrane protein 163 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20220721 MGI PMID:34977916 1332328 Tmem163 transmembrane protein 163 gene MP:0005188 small penis IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0005262 coloboma IAGP N RGD:5509061 20170525 MGI PMID:17470285 1332328 Tmem163 transmembrane protein 163 gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20170525 MGI PMID:27053202 1332328 Tmem163 transmembrane protein 163 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20170525 MGI PMID:22560297 1332328 Tmem163 transmembrane protein 163 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20170525 MGI PMID:27053202 1332328 Tmem163 transmembrane protein 163 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20170525 MGI PMID:19679071 1332328 Tmem163 transmembrane protein 163 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20220721 MGI PMID:33513603 1332328 Tmem163 transmembrane protein 163 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20170525 MGI PMID:12724423 1332328 Tmem163 transmembrane protein 163 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20170525 MGI PMID:17470285 1332328 Tmem163 transmembrane protein 163 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0005575 increased pulmonary ventilation IAGP N RGD:5509061 20170525 MGI PMID:27053202 1332328 Tmem163 transmembrane protein 163 gene MP:0005585 increased tidal volume IAGP N RGD:5509061 20170525 MGI PMID:27053202 1332328 Tmem163 transmembrane protein 163 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20220721 MGI PMID:33513603 1332328 Tmem163 transmembrane protein 163 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231109 MGI PMID:34050709 1332328 Tmem163 transmembrane protein 163 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210520 MGI 1332328 Tmem163 transmembrane protein 163 gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20170525 MGI PMID:21303853 1332328 Tmem163 transmembrane protein 163 gene MP:0006295 absent sclerotome IAGP N RGD:5509061 20170525 MGI PMID:21303853 1332328 Tmem163 transmembrane protein 163 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20170525 MGI PMID:17142319 1332328 Tmem163 transmembrane protein 163 gene MP:0006386 absent somites IAGP N RGD:5509061 20170525 MGI PMID:26932671 1332328 Tmem163 transmembrane protein 163 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20170525 MGI PMID:11316774 1332328 Tmem163 transmembrane protein 163 gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20170525 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20170525 MGI PMID:17142319 1332328 Tmem163 transmembrane protein 163 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20170525 MGI PMID:18316482 1332328 Tmem163 transmembrane protein 163 gene MP:0008862 asymmetric snout IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20170525 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20170525 MGI PMID:15975937 1332328 Tmem163 transmembrane protein 163 gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20170525 MGI PMID:18316482 1332328 Tmem163 transmembrane protein 163 gene MP:0008984 vagina hypoplasia IAGP N RGD:5509061 20170525 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0009066 decreased oviduct weight IAGP N RGD:5509061 20170525 MGI PMID:14676301 1332328 Tmem163 transmembrane protein 163 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20170525 MGI PMID:19679071 1332328 Tmem163 transmembrane protein 163 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20180607 MGI PMID:29222403 1332328 Tmem163 transmembrane protein 163 gene MP:0009199 abnormal external male genitalia morphology IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0009204 absent external male genitalia IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20170525 MGI PMID:15919793 1332328 Tmem163 transmembrane protein 163 gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20170525 MGI PMID:19679071 1332328 Tmem163 transmembrane protein 163 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20220721 MGI PMID:33513603 1332328 Tmem163 transmembrane protein 163 gene MP:0009736 abnormal prostate gland branching morphogenesis IAGP N RGD:5509061 20170525 MGI PMID:18755802 1332328 Tmem163 transmembrane protein 163 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20170525 MGI PMID:27053202 1332328 Tmem163 transmembrane protein 163 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20170525 MGI PMID:11316774 1332328 Tmem163 transmembrane protein 163 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20170525 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 1332328 Tmem163 transmembrane protein 163 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:34050709 1332328 Tmem163 transmembrane protein 163 gene MP:0010487 abnormal right subclavian artery morphology IAGP N RGD:5509061 20231109 MGI PMID:34050709 1332328 Tmem163 transmembrane protein 163 gene MP:0010709 absent eye anterior chamber IAGP N RGD:5509061 20201119 MGI PMID:17470285 1332328 Tmem163 transmembrane protein 163 gene MP:0010734 abnormal paranode morphology IAGP N RGD:5509061 20170525 MGI PMID:20371806 1332328 Tmem163 transmembrane protein 163 gene MP:0010734 abnormal paranode morphology IAGP N RGD:5509061 20170525 MGI PMID:21632923 1332328 Tmem163 transmembrane protein 163 gene MP:0010735 abnormal paranodal axoglial junction morphology IAGP N RGD:5509061 20170525 MGI PMID:21632923 1332328 Tmem163 transmembrane protein 163 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170525 MGI PMID:12724423 1332328 Tmem163 transmembrane protein 163 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170525 MGI PMID:24247431 1332328 Tmem163 transmembrane protein 163 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170525 MGI PMID:11316774 1332328 Tmem163 transmembrane protein 163 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170525 MGI PMID:23677977 1332328 Tmem163 transmembrane protein 163 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230309 MGI PMID:35593225 1332328 Tmem163 transmembrane protein 163 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20170525 MGI PMID:26932671 1332328 Tmem163 transmembrane protein 163 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170525 MGI PMID:16287843 1332328 Tmem163 transmembrane protein 163 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170525 MGI PMID:16287843 1332328 Tmem163 transmembrane protein 163 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20170525 MGI PMID:24589777 1332328 Tmem163 transmembrane protein 163 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20180607 MGI PMID:29222403 1332328 Tmem163 transmembrane protein 163 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20170525 MGI PMID:21303853 1332328 Tmem163 transmembrane protein 163 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20170525 MGI PMID:26932671 1332328 Tmem163 transmembrane protein 163 gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20170525 MGI PMID:24247431 1332328 Tmem163 transmembrane protein 163 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0012176 abnormal head development IAGP N RGD:5509061 20170525 MGI PMID:21303853 1332328 Tmem163 transmembrane protein 163 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20180607 MGI PMID:29222403 1332328 Tmem163 transmembrane protein 163 gene MP:0012724 absent head fold IAGP N RGD:5509061 20170525 MGI PMID:26932671 1332328 Tmem163 transmembrane protein 163 gene MP:0012736 abnormal polar body morphology IAGP N RGD:5509061 20220721 MGI PMID:34977916 1332328 Tmem163 transmembrane protein 163 gene MP:0012755 decreased cranial neural crest cell number IAGP N RGD:5509061 20230309 MGI PMID:35593225 1332328 Tmem163 transmembrane protein 163 gene MP:0012761 increased cranial neural crest cell apoptosis IAGP N RGD:5509061 20230309 MGI PMID:35593225 1332328 Tmem163 transmembrane protein 163 gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0013598 Leydig cell hypertrophy IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:18316482 1332328 Tmem163 transmembrane protein 163 gene MP:0014257 embryonic lethality prior to tooth bud stage, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:25201955 1332328 Tmem163 transmembrane protein 163 gene MP:0014441 decreased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20170525 MGI PMID:12370412 1332328 Tmem163 transmembrane protein 163 gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20220721 MGI PMID:33513603 1332328 Tmem163 transmembrane protein 163 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:22697126 1332328 Tmem163 transmembrane protein 163 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:17470285 1332328 Tmem163 transmembrane protein 163 gene MP:0030189 broad snout IAGP N RGD:5509061 20221020 MGI PMID:32692983 1332328 Tmem163 transmembrane protein 163 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18953638 1332328 Tmem163 transmembrane protein 163 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:29222403 1332328 Tmem163 transmembrane protein 163 gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:15919793 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0001257 increased body length IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0001261 obese IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20240502 MGI PMID:34646989 1332329 Xrn1 5'-3' exoribonuclease 1 gene MP:0014441 decreased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:34646989 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20200310 MGI 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20201231 MGI 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20200310 MGI 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0005354 abnormal ilium morphology IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0008156 decreased diameter of tibia IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20201231 MGI 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0011999 abnormal tail length IEA N RGD:5509061 20201231 MGI 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0014100 increased chondrocyte proliferation IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332333 Cant1 calcium activated nucleotidase 1 gene MP:0030848 short ilium IAGP N RGD:5509061 20220512 MGI PMID:30439444 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:12730604 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0000745 tremors IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:12730604 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:12730604 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:16427626 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:12730604 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:16427626 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12730604 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:16427626 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20181004 MGI PMID:29379136 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16427626 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16427626 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12730604 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16427626 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20181004 MGI PMID:29379136 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001435 absent suckling reflex IAGP N RGD:5509061 20141003 MGI PMID:12730604 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:12730604 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20181004 MGI PMID:29379136 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:12730604 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001524 impaired limb coordination IEA N RGD:5509061 20111116 MGI 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201231 MGI 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001731 abnormal postnatal growth IEA N RGD:5509061 20111116 MGI 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16427626 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0002083 premature death IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0002200 abnormal brain ventricular system morphology IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:16427626 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:12730604 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:12730604 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0005113 decreased spinal cord ventral horn cell number IAGP N RGD:5509061 20141003 MGI PMID:12730604 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0005424 jerky movement IEA N RGD:5509061 20111116 MGI 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20181004 MGI PMID:29379136 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0009393 abnormal resting posture IEA N RGD:5509061 20111116 MGI 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:12730604 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20181004 MGI PMID:29379136 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12730604 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240606 MGI PMID:36933672 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9531547 1332334 Dync1h1 dynein cytoplasmic 1 heavy chain 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IEA N RGD:5509061 20141003 MGI 1332335 Galnt10 polypeptide N-acetylgalactosaminyltransferase 10 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1332336 Grcc10 gene rich cluster, C10 gene gene MP:0001575 cyanosis IEA N RGD:5509061 20210520 MGI 1332336 Grcc10 gene rich cluster, C10 gene gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332339 Rnaseh2c ribonuclease H2, subunit C gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20171026 MGI PMID:22802351 1332339 Rnaseh2c ribonuclease H2, subunit C gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20150430 MGI 1332339 Rnaseh2c ribonuclease H2, subunit C gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20171026 MGI PMID:22802351 1332339 Rnaseh2c ribonuclease H2, subunit C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332340 Antkmt adenine nucleotide translocase lysine methyltransferase gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1332340 Antkmt adenine nucleotide translocase lysine methyltransferase gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1332340 Antkmt adenine nucleotide translocase lysine methyltransferase gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1332340 Antkmt adenine nucleotide translocase lysine methyltransferase gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1332340 Antkmt adenine nucleotide translocase lysine methyltransferase gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1332340 Antkmt adenine nucleotide translocase lysine methyltransferase gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20190808 MGI 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0000562 polydactyly IEA N RGD:5509061 20210520 MGI 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20190808 MGI 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20190808 MGI 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0000897 abnormal midbrain morphology IEA N RGD:5509061 20190808 MGI 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22384391 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:22384391 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:22384391 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190808 MGI 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20190808 MGI 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20190808 MGI 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22384391 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:22384391 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20190808 MGI 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210826 MGI 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0009744 postaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19668215 1332343 Inpp5e inositol polyphosphate-5-phosphatase E gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:19668215 1332347 Mcub mitochondrial calcium uniporter dominant negative beta subunit gene MP:0001284 absent vibrissae IEA N RGD:5509061 20190502 MGI 1332347 Mcub mitochondrial calcium uniporter dominant negative beta subunit gene MP:0001523 impaired righting response IEA N RGD:5509061 20190502 MGI 1332348 Igf2bp3 insulin-like growth factor 2 mRNA binding protein 3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230601 MGI 1332348 Igf2bp3 insulin-like growth factor 2 mRNA binding protein 3 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20220811 MGI 1332348 Igf2bp3 insulin-like growth factor 2 mRNA binding protein 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1332349 Rps21 ribosomal protein S21 gene MP:0000373 belly spot IAGP N RGD:5509061 20210930 MGI PMID:33949947 1332349 Rps21 ribosomal protein S21 gene MP:0000585 kinked tail IAGP N RGD:5509061 20210930 MGI PMID:33949947 1332349 Rps21 ribosomal protein S21 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210930 MGI PMID:33949947 1332349 Rps21 ribosomal protein S21 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210930 MGI PMID:33949947 1332349 Rps21 ribosomal protein S21 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20210930 MGI PMID:33949947 1332349 Rps21 ribosomal protein S21 gene MP:0002083 premature death IAGP N RGD:5509061 20210930 MGI PMID:33949947 1332349 Rps21 ribosomal protein S21 gene MP:0009934 abnormal hind foot hair pigmentation IAGP N RGD:5509061 20210930 MGI PMID:33949947 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16024913 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10760292 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15841208 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16543947 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10655069 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10760292 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11266384 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15841208 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16024913 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16543947 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16691213 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18974039 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20220609 MGI PMID:15026428 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22862945 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22862945 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22862945 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22862945 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:16207713 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:10655069 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10655069 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:16691213 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220609 MGI PMID:15026428 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:10760292 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10655069 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:22862945 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15841208 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18974039 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:10878804 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:10878804 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:16691213 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10878804 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16207713 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220609 MGI PMID:15026428 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10878804 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16691213 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18160655 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10760292 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:16024913 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220609 MGI PMID:15026428 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:10760292 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22862945 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002646 increased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:10760292 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:11266384 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220609 MGI PMID:15026428 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14993927 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20220609 MGI PMID:15026428 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20220609 MGI PMID:15026428 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17992262 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:10655069 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0003192 increased cholesterol efflux IAGP N RGD:5509061 20141003 MGI PMID:17992262 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20141003 MGI PMID:16543947 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20141003 MGI PMID:17992262 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20220609 MGI PMID:15026428 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22862945 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0003981 decreased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:16024913 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18160655 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0004254 cerebral amyloid angiopathy IAGP N RGD:5509061 20141003 MGI PMID:16207713 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22862945 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10655069 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10760292 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11266384 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15841208 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16543947 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16691213 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18974039 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20160929 MGI PMID:27534441 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15841208 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20220609 MGI PMID:15026428 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005401 abnormal fat-soluble vitamin level IAGP N RGD:5509061 20141003 MGI PMID:10655069 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:16024913 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:15163665 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0006084 abnormal circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:10760292 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0006084 abnormal circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:15841208 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22862945 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:22862945 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0008690 increased interleukin-23 secretion IAGP N RGD:5509061 20141003 MGI PMID:22862945 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17992262 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16543947 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0009080 uterus inflammation IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:18160655 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0010161 decreased brain cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18160655 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10878804 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10760292 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16691213 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16207713 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20220609 MGI PMID:15026428 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220609 MGI PMID:15026428 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:10980140 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0031205 decreased circulating phytosterol level IAGP N RGD:5509061 20210211 MGI PMID:14699507 1332354 Abca1 ATP-binding cassette, sub-family A member 1 gene MP:0031632 increased lung cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:18160655 1332355 S100g S100 calcium binding protein G gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:16895982 1332355 S100g S100 calcium binding protein G gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:17696760 1332355 S100g S100 calcium binding protein G gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20200310 MGI PMID:18325990 1332355 S100g S100 calcium binding protein G gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20200310 MGI PMID:18325990 1332356 Abra actin-binding Rho activating protein gene MP:0003410 abnormal artery development IAGP N RGD:5509061 20141003 MGI PMID:19778941 1332356 Abra actin-binding Rho activating protein gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:19778941 1332358 Sirt5 sirtuin 5 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22076378 1332358 Sirt5 sirtuin 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17923681 1332358 Sirt5 sirtuin 5 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20200123 MGI PMID:27681422 1332359 Tanc1 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1332359 Tanc1 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1332359 Tanc1 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1332359 Tanc1 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:21068316 1332359 Tanc1 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:21068316 1332359 Tanc1 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20181227 MGI 1332362 Ssx2ip SSX family member 2 interacting protein gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20190418 MGI 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0010132 decreased DN2 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0010134 decreased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22201126 1332366 Zbtb1 zinc finger and BTB domain containing 1 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18676989 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:23447614 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20200310 MGI PMID:23447614 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:23447614 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:18676989 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:23447614 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:23447614 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0001406 abnormal gait IEA N RGD:5509061 20210128 MGI 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20200310 MGI PMID:23447614 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0001513 limb grasping IEA N RGD:5509061 20210128 MGI 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:18676989 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:23447614 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20200310 MGI PMID:18676989 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:18676989 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20210826 MGI 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0003005 abnormal hippocampal fimbria morphology IAGP N RGD:5509061 20200310 MGI PMID:23447614 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0003006 abnormal hippocampal fornix morphology IAGP N RGD:5509061 20200310 MGI PMID:23447614 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20200310 MGI PMID:18676989 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210826 MGI 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20200310 MGI PMID:23447614 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20200310 MGI PMID:23447614 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20200310 MGI PMID:23447614 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:18676989 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210826 MGI 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20200310 MGI PMID:23447614 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12904583 1332367 Itsn1 intersectin 1 (SH3 domain protein 1A) gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20210128 MGI 1332372 Akap11 A kinase anchor protein 11 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210520 MGI 1332372 Akap11 A kinase anchor protein 11 gene MP:0001258 decreased body length IAGP N RGD:5509061 20160929 MGI PMID:27402760 1332372 Akap11 A kinase anchor protein 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160929 MGI PMID:27402760 1332372 Akap11 A kinase anchor protein 11 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160929 MGI PMID:27402760 1332372 Akap11 A kinase anchor protein 11 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20160929 MGI PMID:27402760 1332372 Akap11 A kinase anchor protein 11 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160929 MGI PMID:27402760 1332372 Akap11 A kinase anchor protein 11 gene MP:0002764 short tibia IAGP N RGD:5509061 20160929 MGI PMID:27402760 1332372 Akap11 A kinase anchor protein 11 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20160929 MGI PMID:27402760 1332372 Akap11 A kinase anchor protein 11 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20160929 MGI PMID:27402760 1332372 Akap11 A kinase anchor protein 11 gene MP:0008055 increased urine osmolality IAGP N RGD:5509061 20160929 MGI PMID:27402760 1332372 Akap11 A kinase anchor protein 11 gene MP:0020211 slow movement IAGP N RGD:5509061 20160929 MGI PMID:27402760 1332373 Adissp adipose secreted signaling protein gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20230223 MGI PMID:36496438 1332373 Adissp adipose secreted signaling protein gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20230223 MGI PMID:36496438 1332373 Adissp adipose secreted signaling protein gene MP:0005331 insulin resistance IAGP N RGD:5509061 20230223 MGI PMID:36496438 1332373 Adissp adipose secreted signaling protein gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20230223 MGI PMID:36496438 1332373 Adissp adipose secreted signaling protein gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20230223 MGI PMID:36496438 1332373 Adissp adipose secreted signaling protein gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20230223 MGI PMID:36496438 1332373 Adissp adipose secreted signaling protein gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20230223 MGI PMID:36496438 1332373 Adissp adipose secreted signaling protein gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20230223 MGI PMID:36496438 1332373 Adissp adipose secreted signaling protein gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20230223 MGI PMID:36496438 1332373 Adissp adipose secreted signaling protein gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20230223 MGI PMID:36496438 1332373 Adissp adipose secreted signaling protein gene MP:0014145 increased white adipose tissue mass IAGP N RGD:5509061 20230223 MGI PMID:36496438 1332373 Adissp adipose secreted signaling protein gene MP:0020426 abnormal beige fat cell physiology IAGP N RGD:5509061 20230223 MGI PMID:36496438 1332373 Adissp adipose secreted signaling protein gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20230223 MGI PMID:36496438 1332374 Exoc3 exocyst complex component 3 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20210325 MGI PMID:33560379 1332374 Exoc3 exocyst complex component 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1332374 Exoc3 exocyst complex component 3 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20210325 MGI PMID:33560379 1332374 Exoc3 exocyst complex component 3 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20210325 MGI PMID:33560379 1332374 Exoc3 exocyst complex component 3 gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20210325 MGI PMID:33560379 1332374 Exoc3 exocyst complex component 3 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20210325 MGI PMID:33560379 1332374 Exoc3 exocyst complex component 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1332374 Exoc3 exocyst complex component 3 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210520 MGI 1332374 Exoc3 exocyst complex component 3 gene MP:0020965 increased platelet dense granule secretion IAGP N RGD:5509061 20210325 MGI PMID:33560379 1332374 Exoc3 exocyst complex component 3 gene MP:0020966 decreased platelet dense granule secretion IAGP N RGD:5509061 20210325 MGI PMID:33560379 1332374 Exoc3 exocyst complex component 3 gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20210325 MGI PMID:33560379 1332375 Olah oleoyl-ACP hydrolase gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20241010 MGI PMID:39137778 1332375 Olah oleoyl-ACP hydrolase gene MP:0000537 abnormal urethra morphology IAGP N RGD:5509061 20241010 MGI PMID:39137778 1332375 Olah oleoyl-ACP hydrolase gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20241010 MGI PMID:39137778 1332375 Olah oleoyl-ACP hydrolase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20241010 MGI PMID:39137778 1332375 Olah oleoyl-ACP hydrolase gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20241010 MGI PMID:39137778 1332375 Olah oleoyl-ACP hydrolase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20241010 MGI PMID:39137778 1332375 Olah oleoyl-ACP hydrolase gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1332375 Olah oleoyl-ACP hydrolase gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20241010 MGI PMID:39137778 1332375 Olah oleoyl-ACP hydrolase gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1332375 Olah oleoyl-ACP hydrolase gene MP:0011485 abnormal urethra urothelium morphology IAGP N RGD:5509061 20241010 MGI PMID:39137778 1332375 Olah oleoyl-ACP hydrolase gene MP:0020947 decreased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20241010 MGI PMID:39137778 1332375 Olah oleoyl-ACP hydrolase gene MP:0031045 decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20241010 MGI PMID:39137778 1332378 Hemgn hemogen gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20220804 MGI PMID:35297980 1332378 Hemgn hemogen gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1332378 Hemgn hemogen gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20220804 MGI PMID:35297980 1332378 Hemgn hemogen gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20220804 MGI PMID:35297980 1332378 Hemgn hemogen gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1332378 Hemgn hemogen gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20220804 MGI PMID:35297980 1332379 Lmf1 lipase maturation factor 1 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:6857276 1332379 Lmf1 lipase maturation factor 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:6857276 1332379 Lmf1 lipase maturation factor 1 gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20151015 MGI PMID:25302068 1332379 Lmf1 lipase maturation factor 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:6857276 1332379 Lmf1 lipase maturation factor 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20151015 MGI PMID:25302068 1332379 Lmf1 lipase maturation factor 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:6857276 1332379 Lmf1 lipase maturation factor 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:6857276 1332379 Lmf1 lipase maturation factor 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:6857276 1332379 Lmf1 lipase maturation factor 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:6857276 1332379 Lmf1 lipase maturation factor 1 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:6857276 1332379 Lmf1 lipase maturation factor 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:6857276 1332379 Lmf1 lipase maturation factor 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20151015 MGI PMID:25302068 1332379 Lmf1 lipase maturation factor 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:6857276 1332379 Lmf1 lipase maturation factor 1 gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:6857276 1332379 Lmf1 lipase maturation factor 1 gene MP:0009699 hyperchylomicronemia IAGP N RGD:5509061 20141003 MGI PMID:6857276 1332379 Lmf1 lipase maturation factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20151015 MGI PMID:25302068 1332379 Lmf1 lipase maturation factor 1 gene MP:0011579 decreased lipoprotein lipase activity IAGP N RGD:5509061 20141003 MGI PMID:3972797 1332379 Lmf1 lipase maturation factor 1 gene MP:0011579 decreased lipoprotein lipase activity IAGP N RGD:5509061 20141003 MGI PMID:6857276 1332379 Lmf1 lipase maturation factor 1 gene MP:0011579 decreased lipoprotein lipase activity IAGP N RGD:5509061 20151015 MGI PMID:25302068 1332379 Lmf1 lipase maturation factor 1 gene MP:0011582 decreased triglyceride lipase activity IAGP N RGD:5509061 20141003 MGI PMID:6857276 1332379 Lmf1 lipase maturation factor 1 gene MP:0011582 decreased triglyceride lipase activity IAGP N RGD:5509061 20151015 MGI PMID:25302068 1332381 Mtmr14 myotubularin related protein 14 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:19465920 1332381 Mtmr14 myotubularin related protein 14 gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0001147 small testis IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19465920 1332381 Mtmr14 myotubularin related protein 14 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19465920 1332381 Mtmr14 myotubularin related protein 14 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:19465920 1332381 Mtmr14 myotubularin related protein 14 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19465920 1332381 Mtmr14 myotubularin related protein 14 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19465920 1332381 Mtmr14 myotubularin related protein 14 gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:19465920 1332381 Mtmr14 myotubularin related protein 14 gene MP:0004036 abnormal muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:19465920 1332381 Mtmr14 myotubularin related protein 14 gene MP:0004089 dilated sarcoplasmic reticulum IAGP N RGD:5509061 20141003 MGI PMID:19465920 1332381 Mtmr14 myotubularin related protein 14 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19465920 1332381 Mtmr14 myotubularin related protein 14 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:19465920 1332381 Mtmr14 myotubularin related protein 14 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332381 Mtmr14 myotubularin related protein 14 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20220609 MGI PMID:30412589 1332387 Patl1 protein associated with topoisomerase II homolog 1 (yeast) gene MP:0000745 tremors IEA N RGD:5509061 20201231 MGI 1332387 Patl1 protein associated with topoisomerase II homolog 1 (yeast) gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1332387 Patl1 protein associated with topoisomerase II homolog 1 (yeast) gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1332387 Patl1 protein associated with topoisomerase II homolog 1 (yeast) gene MP:0010053 decreased grip strength IEA N RGD:5509061 20190502 MGI 1332387 Patl1 protein associated with topoisomerase II homolog 1 (yeast) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1332387 Patl1 protein associated with topoisomerase II homolog 1 (yeast) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332387 Patl1 protein associated with topoisomerase II homolog 1 (yeast) gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1332388 Kifc2 kinesin family member C2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1332388 Kifc2 kinesin family member C2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:11259594 1332389 Adprm ADP-ribose/CDP-alcohol diphosphatase, manganese dependent gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210128 MGI 1332389 Adprm ADP-ribose/CDP-alcohol diphosphatase, manganese dependent gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1332389 Adprm ADP-ribose/CDP-alcohol diphosphatase, manganese dependent gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1332389 Adprm ADP-ribose/CDP-alcohol diphosphatase, manganese dependent gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210520 MGI 1332389 Adprm ADP-ribose/CDP-alcohol diphosphatase, manganese dependent gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201231 MGI 1332389 Adprm ADP-ribose/CDP-alcohol diphosphatase, manganese dependent gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20211021 MGI 1332389 Adprm ADP-ribose/CDP-alcohol diphosphatase, manganese dependent gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1332390 Fam216a family with sequence similarity 216, member A gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1332390 Fam216a family with sequence similarity 216, member A gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1332391 Pkig protein kinase inhibitor, gamma gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1332391 Pkig protein kinase inhibitor, gamma gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20181227 MGI 1332391 Pkig protein kinase inhibitor, gamma gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1332391 Pkig protein kinase inhibitor, gamma gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1332391 Pkig protein kinase inhibitor, gamma gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1332391 Pkig protein kinase inhibitor, gamma gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1332391 Pkig protein kinase inhibitor, gamma gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1332391 Pkig protein kinase inhibitor, gamma gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1332391 Pkig protein kinase inhibitor, gamma gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1332391 Pkig protein kinase inhibitor, gamma gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1332393 Fstl1 follistatin-like 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20210520 MGI 1332393 Fstl1 follistatin-like 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20200310 MGI PMID:22485132 1332393 Fstl1 follistatin-like 1 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20200310 MGI PMID:22485132 1332393 Fstl1 follistatin-like 1 gene MP:0000536 hydroureter IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0000536 hydroureter IAGP N RGD:5509061 20200310 MGI PMID:22485132 1332393 Fstl1 follistatin-like 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:21382556 1332393 Fstl1 follistatin-like 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1332393 Fstl1 follistatin-like 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:21987816 1332393 Fstl1 follistatin-like 1 gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20220407 MGI PMID:31834999 1332393 Fstl1 follistatin-like 1 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20220407 MGI PMID:31834999 1332393 Fstl1 follistatin-like 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20220407 MGI PMID:31834999 1332393 Fstl1 follistatin-like 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:20861081 1332393 Fstl1 follistatin-like 1 gene MP:0002249 abnormal larynx morphology IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20200310 MGI PMID:21382556 1332393 Fstl1 follistatin-like 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20200310 MGI PMID:21987816 1332393 Fstl1 follistatin-like 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20200310 MGI PMID:22485132 1332393 Fstl1 follistatin-like 1 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200310 MGI PMID:21987816 1332393 Fstl1 follistatin-like 1 gene MP:0003586 dilated ureter IAGP N RGD:5509061 20200310 MGI PMID:22485132 1332393 Fstl1 follistatin-like 1 gene MP:0003588 ureter stenosis IAGP N RGD:5509061 20200310 MGI PMID:22485132 1332393 Fstl1 follistatin-like 1 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20200310 MGI PMID:22485132 1332393 Fstl1 follistatin-like 1 gene MP:0003856 abnormal hindlimb stylopod morphology IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20200310 MGI PMID:21987816 1332393 Fstl1 follistatin-like 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:21382556 1332393 Fstl1 follistatin-like 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20200310 MGI PMID:22485132 1332393 Fstl1 follistatin-like 1 gene MP:0004202 pulmonary hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0004372 bowed fibula IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20200310 MGI PMID:21987816 1332393 Fstl1 follistatin-like 1 gene MP:0004551 decreased tracheal cartilage ring number IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20200310 MGI PMID:21987816 1332393 Fstl1 follistatin-like 1 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0004694 absent patella IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 1332393 Fstl1 follistatin-like 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1332393 Fstl1 follistatin-like 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20201022 MGI 1332393 Fstl1 follistatin-like 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200310 MGI PMID:21382556 1332393 Fstl1 follistatin-like 1 gene MP:0005440 increased glycogen level IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20200310 MGI PMID:21987816 1332393 Fstl1 follistatin-like 1 gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20200310 MGI PMID:21987816 1332393 Fstl1 follistatin-like 1 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0006432 abnormal costal cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0008532 decreased chemical nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:21382556 1332393 Fstl1 follistatin-like 1 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20200310 MGI PMID:21987816 1332393 Fstl1 follistatin-like 1 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:21987816 1332393 Fstl1 follistatin-like 1 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20200310 MGI PMID:21987816 1332393 Fstl1 follistatin-like 1 gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0010816 decreased type I pneumocyte number IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0010883 trachea stenosis IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0010890 decreased alveolar lamellar body number IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20220407 MGI PMID:31834999 1332393 Fstl1 follistatin-like 1 gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0010950 abnormal lung hysteresivity IAGP N RGD:5509061 20220407 MGI PMID:31834999 1332393 Fstl1 follistatin-like 1 gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0011045 decreased lung elastance IAGP N RGD:5509061 20220407 MGI PMID:31834999 1332393 Fstl1 follistatin-like 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21482757 1332393 Fstl1 follistatin-like 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0011304 kidney papillary atrophy IAGP N RGD:5509061 20200310 MGI PMID:22485132 1332393 Fstl1 follistatin-like 1 gene MP:0011484 abnormal ureter urothelium morphology IAGP N RGD:5509061 20200310 MGI PMID:22485132 1332393 Fstl1 follistatin-like 1 gene MP:0011505 camptomelia IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1332393 Fstl1 follistatin-like 1 gene MP:0014378 increased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:21382556 1332393 Fstl1 follistatin-like 1 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0030002 increased lung apoptosis IAGP N RGD:5509061 20220407 MGI PMID:31834999 1332393 Fstl1 follistatin-like 1 gene MP:0030859 absent sesamoid bone of gastrocnemius IAGP N RGD:5509061 20200310 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:21826198 1332393 Fstl1 follistatin-like 1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:21987816 1332397 Ndufaf6 NADH:ubiquinone oxidoreductase complex assembly factor 6 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1332398 Adap1 ArfGAP with dual PH domains 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20230126 MGI PMID:33139322 1332398 Adap1 ArfGAP with dual PH domains 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:31792062 1332398 Adap1 ArfGAP with dual PH domains 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20230126 MGI PMID:33139322 1332398 Adap1 ArfGAP with dual PH domains 1 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20201231 MGI 1332398 Adap1 ArfGAP with dual PH domains 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20230126 MGI PMID:33139322 1332398 Adap1 ArfGAP with dual PH domains 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20230126 MGI PMID:33139322 1332398 Adap1 ArfGAP with dual PH domains 1 gene MP:0013426 decreased memory-marker NK cell number IEA N RGD:5509061 20201231 MGI 1332398 Adap1 ArfGAP with dual PH domains 1 gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20230126 MGI PMID:33139322 1332398 Adap1 ArfGAP with dual PH domains 1 gene MP:0020507 increased dendritic spine density IAGP N RGD:5509061 20230126 MGI PMID:33139322 1332399 Bco1 beta-carotene oxygenase 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17855355 1332399 Bco1 beta-carotene oxygenase 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17855355 1332399 Bco1 beta-carotene oxygenase 1 gene MP:0004019 abnormal vitamin homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17855355 1332399 Bco1 beta-carotene oxygenase 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17855355 1332399 Bco1 beta-carotene oxygenase 1 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17855355 1332399 Bco1 beta-carotene oxygenase 1 gene MP:0011232 abnormal vitamin A level IAGP N RGD:5509061 20141003 MGI PMID:17855355 1332399 Bco1 beta-carotene oxygenase 1 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:17855355 1332400 Rnf43 ring finger protein 43 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1332400 Rnf43 ring finger protein 43 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20200423 MGI PMID:30884828 1332400 Rnf43 ring finger protein 43 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1332400 Rnf43 ring finger protein 43 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22895187 1332400 Rnf43 ring finger protein 43 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1332400 Rnf43 ring finger protein 43 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20230119 MGI 1332400 Rnf43 ring finger protein 43 gene MP:0002764 short tibia IEA N RGD:5509061 20230119 MGI 1332400 Rnf43 ring finger protein 43 gene MP:0002814 hyperchromasia IAGP N RGD:5509061 20200423 MGI PMID:30884828 1332400 Rnf43 ring finger protein 43 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20200423 MGI PMID:30884828 1332400 Rnf43 ring finger protein 43 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22895187 1332400 Rnf43 ring finger protein 43 gene MP:0005213 gastric metaplasia IAGP N RGD:5509061 20200423 MGI PMID:30884828 1332400 Rnf43 ring finger protein 43 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1332400 Rnf43 ring finger protein 43 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20230119 MGI 1332400 Rnf43 ring finger protein 43 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20230119 MGI 1332400 Rnf43 ring finger protein 43 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200423 MGI PMID:30884828 1332400 Rnf43 ring finger protein 43 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230119 MGI 1332400 Rnf43 ring finger protein 43 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230119 MGI 1332400 Rnf43 ring finger protein 43 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22895187 1332400 Rnf43 ring finger protein 43 gene MP:0010783 abnormal stomach wall morphology IAGP N RGD:5509061 20200423 MGI PMID:30380024 1332400 Rnf43 ring finger protein 43 gene MP:0010783 abnormal stomach wall morphology IAGP N RGD:5509061 20200423 MGI PMID:30884828 1332400 Rnf43 ring finger protein 43 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20200423 MGI PMID:30380024 1332400 Rnf43 ring finger protein 43 gene MP:0013485 increased Paneth cell number IAGP N RGD:5509061 20150312 MGI PMID:22895187 1332400 Rnf43 ring finger protein 43 gene MP:0013578 abnormal stomach glandular region morphology IAGP N RGD:5509061 20200423 MGI PMID:30380024 1332402 Fam81a family with sequence similarity 81, member A gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1332402 Fam81a family with sequence similarity 81, member A gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1332402 Fam81a family with sequence similarity 81, member A gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220519 MGI 1332402 Fam81a family with sequence similarity 81, member A gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220519 MGI 1332402 Fam81a family with sequence similarity 81, member A gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220519 MGI 1332402 Fam81a family with sequence similarity 81, member A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1332403 Anks3 ankyrin repeat and sterile alpha motif domain containing 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332404 Cnbp cellular nucleic acid binding protein gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200310 MGI 1332404 Cnbp cellular nucleic acid binding protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20230601 MGI 1332404 Cnbp cellular nucleic acid binding protein gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1332404 Cnbp cellular nucleic acid binding protein gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0004388 absent prechordal plate IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0004592 small mandible IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 1332404 Cnbp cellular nucleic acid binding protein gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20230601 MGI 1332404 Cnbp cellular nucleic acid binding protein gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20230601 MGI 1332404 Cnbp cellular nucleic acid binding protein gene MP:0008533 abnormal anterior visceral endoderm morphology IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332404 Cnbp cellular nucleic acid binding protein gene MP:0011257 abnormal head fold morphology IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0012517 absent diencephalon IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0012683 absent telencephalon IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0012706 decreased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0013185 absent anterior definitive endoderm IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332404 Cnbp cellular nucleic acid binding protein gene MP:0013505 decreased embryonic tissue cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:12588852 1332405 Tmem87a transmembrane protein 87A gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20240404 MGI PMID:38422143 1332405 Tmem87a transmembrane protein 87A gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20240404 MGI PMID:38422143 1332405 Tmem87a transmembrane protein 87A gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20240404 MGI PMID:38422143 1332405 Tmem87a transmembrane protein 87A gene MP:0010055 abnormal sensory neuron physiology IAGP N RGD:5509061 20240404 MGI PMID:38422143 1332406 Mnd1 meiotic nuclear divisions 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:24304900 1332406 Mnd1 meiotic nuclear divisions 1 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:24304900 1332406 Mnd1 meiotic nuclear divisions 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:24304900 1332406 Mnd1 meiotic nuclear divisions 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:24304900 1332407 Ciao2b cytosolic iron-sulfur assembly component 2B gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1332407 Ciao2b cytosolic iron-sulfur assembly component 2B gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1332407 Ciao2b cytosolic iron-sulfur assembly component 2B gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1332407 Ciao2b cytosolic iron-sulfur assembly component 2B gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1332407 Ciao2b cytosolic iron-sulfur assembly component 2B gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1332407 Ciao2b cytosolic iron-sulfur assembly component 2B gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1332407 Ciao2b cytosolic iron-sulfur assembly component 2B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1332407 Ciao2b cytosolic iron-sulfur assembly component 2B gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1332407 Ciao2b cytosolic iron-sulfur assembly component 2B gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1332408 Mri1 methylthioribose-1-phosphate isomerase 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230601 MGI 1332409 Guf1 GUF1 homolog, GTPase gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20230316 MGI PMID:27065197 1332409 Guf1 GUF1 homolog, GTPase gene MP:0001925 male infertility IAGP N RGD:5509061 20230316 MGI PMID:27065197 1332409 Guf1 GUF1 homolog, GTPase gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20230316 MGI PMID:27065197 1332409 Guf1 GUF1 homolog, GTPase gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230316 MGI PMID:27065197 1332409 Guf1 GUF1 homolog, GTPase gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230316 MGI PMID:27065197 1332409 Guf1 GUF1 homolog, GTPase gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20230316 MGI PMID:27065197 1332409 Guf1 GUF1 homolog, GTPase gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230316 MGI PMID:27065197 1332409 Guf1 GUF1 homolog, GTPase gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20230316 MGI PMID:27065197 1332409 Guf1 GUF1 homolog, GTPase gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20230316 MGI PMID:27065197 1332409 Guf1 GUF1 homolog, GTPase gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20230316 MGI PMID:27065197 1332409 Guf1 GUF1 homolog, GTPase gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20230316 MGI PMID:27065197 1332410 Nde1 nudE neurodevelopment protein 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:15473967 1332410 Nde1 nudE neurodevelopment protein 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15473967 1332410 Nde1 nudE neurodevelopment protein 1 gene MP:0000821 choroid plexus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23673330 1332410 Nde1 nudE neurodevelopment protein 1 gene MP:0000923 abnormal roof plate morphology IAGP N RGD:5509061 20141003 MGI PMID:23673330 1332410 Nde1 nudE neurodevelopment protein 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:23673330 1332410 Nde1 nudE neurodevelopment protein 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:15473967 1332410 Nde1 nudE neurodevelopment protein 1 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:15473967 1332410 Nde1 nudE neurodevelopment protein 1 gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:23673330 1332410 Nde1 nudE neurodevelopment protein 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:15473967 1332410 Nde1 nudE neurodevelopment protein 1 gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:23673330 1332410 Nde1 nudE neurodevelopment protein 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23673330 1332410 Nde1 nudE neurodevelopment protein 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15473967 1332410 Nde1 nudE neurodevelopment protein 1 gene MP:0021091 abnormal dorsal interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:23673330 1332414 Gid8 GID complex subunit 8 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20240523 MGI 1332414 Gid8 GID complex subunit 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20181004 MGI PMID:25753038 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19492146 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19492146 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:15879509 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:19492146 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:19492146 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:19492146 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:19492146 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:19492146 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:19492146 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19492146 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20181004 MGI PMID:25753038 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0011922 abnormal circulating osteocalcin level IAGP N RGD:5509061 20181004 MGI PMID:25753038 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0031117 subdural hemorrhage IAGP N RGD:5509061 20200917 MGI PMID:19492146 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0031136 muscle hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:19492146 1332416 Vkorc1 vitamin K epoxide reductase complex, subunit 1 gene MP:0031152 subcutaneous hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:19492146 1332417 Tmt1b thiol methyltransferase 1B gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20230720 MGI 1332417 Tmt1b thiol methyltransferase 1B gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20230720 MGI 1332417 Tmt1b thiol methyltransferase 1B gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230720 MGI 1332419 Emc6 ER membrane protein complex subunit 6 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1332419 Emc6 ER membrane protein complex subunit 6 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20231207 MGI 1332419 Emc6 ER membrane protein complex subunit 6 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1332419 Emc6 ER membrane protein complex subunit 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332419 Emc6 ER membrane protein complex subunit 6 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1332419 Emc6 ER membrane protein complex subunit 6 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1332420 Tspoap1 TSPO associated protein 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1332420 Tspoap1 TSPO associated protein 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20180308 MGI PMID:27671655 1332420 Tspoap1 TSPO associated protein 1 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20180308 MGI PMID:27671655 1332420 Tspoap1 TSPO associated protein 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1332420 Tspoap1 TSPO associated protein 1 gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20180308 MGI PMID:27671655 1332420 Tspoap1 TSPO associated protein 1 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20180308 MGI PMID:27671655 1332420 Tspoap1 TSPO associated protein 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20240523 MGI 1332420 Tspoap1 TSPO associated protein 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20240523 MGI 1332420 Tspoap1 TSPO associated protein 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1332420 Tspoap1 TSPO associated protein 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230601 MGI 1332420 Tspoap1 TSPO associated protein 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1332421 Galnt13 polypeptide N-acetylgalactosaminyltransferase 13 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1332421 Galnt13 polypeptide N-acetylgalactosaminyltransferase 13 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1332421 Galnt13 polypeptide N-acetylgalactosaminyltransferase 13 gene MP:0000692 small spleen IEA N RGD:5509061 20220519 MGI 1332421 Galnt13 polypeptide N-acetylgalactosaminyltransferase 13 gene MP:0001304 cataract IEA N RGD:5509061 20210826 MGI 1332421 Galnt13 polypeptide N-acetylgalactosaminyltransferase 13 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1332421 Galnt13 polypeptide N-acetylgalactosaminyltransferase 13 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1332421 Galnt13 polypeptide N-acetylgalactosaminyltransferase 13 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1332421 Galnt13 polypeptide N-acetylgalactosaminyltransferase 13 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1332421 Galnt13 polypeptide N-acetylgalactosaminyltransferase 13 gene MP:0002989 small kidney IEA N RGD:5509061 20201022 MGI 1332421 Galnt13 polypeptide N-acetylgalactosaminyltransferase 13 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20221215 MGI 1332422 Camkmt calmodulin-lysine N-methyltransferase gene MP:0000751 myopathy IAGP N RGD:5509061 20161103 MGI PMID:26247364 1332422 Camkmt calmodulin-lysine N-methyltransferase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161103 MGI PMID:26247364 1332422 Camkmt calmodulin-lysine N-methyltransferase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20161103 MGI PMID:26247364 1332422 Camkmt calmodulin-lysine N-methyltransferase gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20160421 MGI 1332422 Camkmt calmodulin-lysine N-methyltransferase gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20161103 MGI PMID:26247364 1332422 Camkmt calmodulin-lysine N-methyltransferase gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20161103 MGI PMID:26247364 1332422 Camkmt calmodulin-lysine N-methyltransferase gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20160421 MGI 1332422 Camkmt calmodulin-lysine N-methyltransferase gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20181227 MGI 1332422 Camkmt calmodulin-lysine N-methyltransferase gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1332422 Camkmt calmodulin-lysine N-methyltransferase gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20161103 MGI PMID:26247364 1332422 Camkmt calmodulin-lysine N-methyltransferase gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1332422 Camkmt calmodulin-lysine N-methyltransferase gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20161103 MGI PMID:26247364 1332422 Camkmt calmodulin-lysine N-methyltransferase gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20161103 MGI PMID:26247364 1332422 Camkmt calmodulin-lysine N-methyltransferase gene MP:0021165 behavioral developmental delay IAGP N RGD:5509061 20220922 MGI PMID:26247364 1332425 Tmem175 transmembrane protein 175 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20210506 MGI PMID:33505021 1332425 Tmem175 transmembrane protein 175 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210506 MGI PMID:33505021 1332425 Tmem175 transmembrane protein 175 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1332425 Tmem175 transmembrane protein 175 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210826 MGI 1332425 Tmem175 transmembrane protein 175 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20210506 MGI PMID:33505021 1332425 Tmem175 transmembrane protein 175 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20210506 MGI PMID:33505021 1332425 Tmem175 transmembrane protein 175 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20210506 MGI PMID:33505021 1332425 Tmem175 transmembrane protein 175 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1332425 Tmem175 transmembrane protein 175 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20210506 MGI PMID:33505021 1332425 Tmem175 transmembrane protein 175 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20210506 MGI PMID:33505021 1332425 Tmem175 transmembrane protein 175 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20210506 MGI PMID:33505021 1332425 Tmem175 transmembrane protein 175 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20210506 MGI PMID:33505021 1332425 Tmem175 transmembrane protein 175 gene MP:0008407 decreased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20210506 MGI PMID:33505021 1332425 Tmem175 transmembrane protein 175 gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20210506 MGI PMID:33505021 1332425 Tmem175 transmembrane protein 175 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20220519 MGI 1332427 Septin3 septin 3 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1332427 Septin3 septin 3 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20211021 MGI 1332427 Septin3 septin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10446280 1332427 Septin3 septin 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332428 Car4 carbonic anhydrase 4 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 1332428 Car4 carbonic anhydrase 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16260723 1332428 Car4 carbonic anhydrase 4 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16260723 1332428 Car4 carbonic anhydrase 4 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16260723 1332428 Car4 carbonic anhydrase 4 gene MP:0004043 abnormal pH regulation IAGP N RGD:5509061 20141003 MGI PMID:16260723 1332428 Car4 carbonic anhydrase 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 1332428 Car4 carbonic anhydrase 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220811 MGI 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0000274 enlarged heart IEA N RGD:5509061 20220811 MGI 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230406 MGI PMID:33188300 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20230601 MGI 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220811 MGI 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0002064 seizures IAGP N RGD:5509061 20230406 MGI PMID:33188300 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20230406 MGI PMID:33188300 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20230406 MGI PMID:33188300 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0005202 lethargy IAGP N RGD:5509061 20230406 MGI PMID:33188300 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220811 MGI 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20230406 MGI PMID:33188300 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210520 MGI 1332429 Hpdl 4-hydroxyphenylpyruvate dioxygenase-like gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1332432 Odad1 outer dynein arm docking complex subunit 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210520 MGI 1332433 Cluh clustered mitochondria homolog gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20180322 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180322 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180322 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1332433 Cluh clustered mitochondria homolog gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200514 MGI 1332433 Cluh clustered mitochondria homolog gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20180322 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20200514 MGI 1332433 Cluh clustered mitochondria homolog gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20200514 MGI 1332433 Cluh clustered mitochondria homolog gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180322 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20200514 MGI 1332433 Cluh clustered mitochondria homolog gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20210520 MGI 1332433 Cluh clustered mitochondria homolog gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20180322 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20180322 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20240523 MGI 1332433 Cluh clustered mitochondria homolog gene MP:0009138 increased brown fat lipid droplet number IAGP N RGD:5509061 20180322 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20180322 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20180322 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20180322 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180322 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332433 Cluh clustered mitochondria homolog gene MP:0011637 abnormal mitochondrial matrix morphology IAGP N RGD:5509061 20180322 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20180322 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0013676 increased Ly6C-positive mature NK cell number IEA N RGD:5509061 20210826 MGI 1332433 Cluh clustered mitochondria homolog gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0030644 increased circulating methionine level IAGP N RGD:5509061 20180920 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0030667 increased circulating proline level IAGP N RGD:5509061 20180920 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0030694 increased circulating serine level IAGP N RGD:5509061 20180927 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0030703 increased circulating threonine level IAGP N RGD:5509061 20180927 MGI PMID:28188211 1332433 Cluh clustered mitochondria homolog gene MP:0030718 increased circulating lysine level IAGP N RGD:5509061 20180927 MGI PMID:28188211 1332434 Plekho2 pleckstrin homology domain containing, family O member 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20191024 MGI PMID:28627369 1332434 Plekho2 pleckstrin homology domain containing, family O member 2 gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20191024 MGI PMID:28627369 1332436 Sgsm3 small G protein signaling modulator 3 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 1332436 Sgsm3 small G protein signaling modulator 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1332436 Sgsm3 small G protein signaling modulator 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1332439 Arfgef2 ADP ribosylation factor guanine nucleotide exchange factor 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22956851 1332439 Arfgef2 ADP ribosylation factor guanine nucleotide exchange factor 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22956851 1332439 Arfgef2 ADP ribosylation factor guanine nucleotide exchange factor 2 gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20141003 MGI PMID:22956851 1332439 Arfgef2 ADP ribosylation factor guanine nucleotide exchange factor 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:22956851 1332439 Arfgef2 ADP ribosylation factor guanine nucleotide exchange factor 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20857375 1332439 Arfgef2 ADP ribosylation factor guanine nucleotide exchange factor 2 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20141003 MGI PMID:22956851 1332441 Rtca RNA 3'-terminal phosphate cyclase gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20161124 MGI PMID:25961792 1332441 Rtca RNA 3'-terminal phosphate cyclase gene MP:0030013 enhanced central nervous system regeneration IAGP N RGD:5509061 20170713 MGI PMID:25961792 1332442 Trib1 tribbles pseudokinase 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1332442 Trib1 tribbles pseudokinase 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23515163 1332442 Trib1 tribbles pseudokinase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17724128 1332442 Trib1 tribbles pseudokinase 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1332442 Trib1 tribbles pseudokinase 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20190502 MGI 1332442 Trib1 tribbles pseudokinase 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1332442 Trib1 tribbles pseudokinase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17724128 1332442 Trib1 tribbles pseudokinase 1 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:23515163 1332442 Trib1 tribbles pseudokinase 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:23515163 1332442 Trib1 tribbles pseudokinase 1 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23515163 1332442 Trib1 tribbles pseudokinase 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23515163 1332442 Trib1 tribbles pseudokinase 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23515163 1332442 Trib1 tribbles pseudokinase 1 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:23515163 1332442 Trib1 tribbles pseudokinase 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23515163 1332442 Trib1 tribbles pseudokinase 1 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:17724128 1332442 Trib1 tribbles pseudokinase 1 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:23515163 1332442 Trib1 tribbles pseudokinase 1 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:23515163 1332442 Trib1 tribbles pseudokinase 1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23515163 1332442 Trib1 tribbles pseudokinase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332442 Trib1 tribbles pseudokinase 1 gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20141003 MGI PMID:23515163 1332442 Trib1 tribbles pseudokinase 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1332446 Mss51 MSS51 mitochondrial translational activator gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20191205 MGI PMID:29913553 1332446 Mss51 MSS51 mitochondrial translational activator gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20191205 MGI PMID:29913553 1332446 Mss51 MSS51 mitochondrial translational activator gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20191205 MGI PMID:29913553 1332446 Mss51 MSS51 mitochondrial translational activator gene MP:0002981 increased liver weight IAGP N RGD:5509061 20191205 MGI PMID:29913553 1332446 Mss51 MSS51 mitochondrial translational activator gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20191205 MGI PMID:29913553 1332446 Mss51 MSS51 mitochondrial translational activator gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20191205 MGI PMID:29913553 1332446 Mss51 MSS51 mitochondrial translational activator gene MP:0005331 insulin resistance IAGP N RGD:5509061 20191205 MGI PMID:29913553 1332446 Mss51 MSS51 mitochondrial translational activator gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20191205 MGI PMID:29913553 1332446 Mss51 MSS51 mitochondrial translational activator gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20191205 MGI PMID:29913553 1332446 Mss51 MSS51 mitochondrial translational activator gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20191205 MGI PMID:29913553 1332446 Mss51 MSS51 mitochondrial translational activator gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20191205 MGI PMID:29913553 1332446 Mss51 MSS51 mitochondrial translational activator gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20191205 MGI PMID:29913553 1332446 Mss51 MSS51 mitochondrial translational activator gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20191205 MGI PMID:29913553 1332446 Mss51 MSS51 mitochondrial translational activator gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20191205 MGI PMID:29913553 1332446 Mss51 MSS51 mitochondrial translational activator gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20191205 MGI PMID:29913553 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16493085 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22432050 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17997333 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22432050 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20141003 MGI PMID:21159799 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:11911824 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:17997333 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17997333 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17997333 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002148 abnormal hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002194 maximal tonic hindlimb extension seizures IAGP N RGD:5509061 20141003 MGI PMID:21159799 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18949059 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8552190 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18949059 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:8552190 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23109709 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:8552190 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:8552190 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:10981970 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:22432050 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:12528127 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:23109709 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:22432050 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:21159799 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23109709 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:17997333 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:17997333 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:17446931 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:23109709 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17435165 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18949059 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:8552190 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008121 increased myeloid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:23109709 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:23109709 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:8552190 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:8552190 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:8552190 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:23109709 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:8552190 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008524 increased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:22432050 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:23123062 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23109709 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17997333 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0009646 urinary bladder inflammation IAGP N RGD:5509061 20141003 MGI PMID:22432050 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0011508 abnormal glomerular capillary thrombosis IAGP N RGD:5509061 20141003 MGI PMID:21724994 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:23109709 1332447 Fcgr2b Fc receptor, IgG, low affinity IIb gene MP:0020993 abnormal urine cytokine level IAGP N RGD:5509061 20210408 MGI PMID:22432050 1332449 Ogfod3 2-oxoglutarate and iron-dependent oxygenase domain containing 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20170105 MGI 1332449 Ogfod3 2-oxoglutarate and iron-dependent oxygenase domain containing 3 gene MP:0001512 trunk curl IEA N RGD:5509061 20190502 MGI 1332449 Ogfod3 2-oxoglutarate and iron-dependent oxygenase domain containing 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1332450 Faap100 Fanconi anemia core complex associated protein 100 gene MP:0001127 small ovary IAGP N RGD:5509061 20231130 MGI PMID:37580696 1332450 Faap100 Fanconi anemia core complex associated protein 100 gene MP:0001147 small testis IAGP N RGD:5509061 20231130 MGI PMID:37580696 1332450 Faap100 Fanconi anemia core complex associated protein 100 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20231130 MGI PMID:37580696 1332450 Faap100 Fanconi anemia core complex associated protein 100 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20231130 MGI PMID:37580696 1332450 Faap100 Fanconi anemia core complex associated protein 100 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20231130 MGI PMID:37580696 1332450 Faap100 Fanconi anemia core complex associated protein 100 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20231130 MGI PMID:37580696 1332450 Faap100 Fanconi anemia core complex associated protein 100 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20231130 MGI PMID:37580696 1332450 Faap100 Fanconi anemia core complex associated protein 100 gene MP:0005159 azoospermia IAGP N RGD:5509061 20231130 MGI PMID:37580696 1332450 Faap100 Fanconi anemia core complex associated protein 100 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20231130 MGI PMID:37580696 1332450 Faap100 Fanconi anemia core complex associated protein 100 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20231130 MGI PMID:37580696 1332450 Faap100 Fanconi anemia core complex associated protein 100 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20231130 MGI PMID:37580696 1332450 Faap100 Fanconi anemia core complex associated protein 100 gene MP:0030934 decreased primordial germ cell proliferation IAGP N RGD:5509061 20231130 MGI PMID:37580696 1332450 Faap100 Fanconi anemia core complex associated protein 100 gene MP:0030935 increased primordial germ cell apoptosis IAGP N RGD:5509061 20231130 MGI PMID:37580696 1332452 Rasd2 RASD family, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15199135 1332452 Rasd2 RASD family, member 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15199135 1332452 Rasd2 RASD family, member 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15199135 1332452 Rasd2 RASD family, member 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15199135 1332452 Rasd2 RASD family, member 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:15199135 1332453 Ctsm cathepsin M gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20181227 MGI 1332453 Ctsm cathepsin M gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1332453 Ctsm cathepsin M gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20181227 MGI 1332453 Ctsm cathepsin M gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20201022 MGI 1332453 Ctsm cathepsin M gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:24469635 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:24469635 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0000884 delaminated Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:24469635 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180201 MGI PMID:19503083 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180201 MGI PMID:23936174 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20180201 MGI PMID:23936174 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:24469635 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0002690 akinesia IAGP N RGD:5509061 20180201 MGI PMID:19503083 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20180201 MGI PMID:23936174 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20180201 MGI PMID:19503083 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0003267 constipation IAGP N RGD:5509061 20180201 MGI PMID:23936174 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20180201 MGI PMID:19503083 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20180201 MGI PMID:23936174 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20180201 MGI PMID:19503083 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0005036 diarrhea IAGP N RGD:5509061 20180201 MGI PMID:23936174 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20180201 MGI PMID:19503083 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20180201 MGI PMID:19503083 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20180201 MGI PMID:23455607 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20180201 MGI PMID:23455607 1332454 Khdrbs2 KH domain containing, RNA binding, signal transduction associated 2 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:24469635 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:20709292 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:20709292 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:20709292 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20200310 MGI PMID:20709292 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20200310 MGI PMID:20709292 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:20709292 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:12649138 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20200310 MGI PMID:12649138 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20200310 MGI PMID:19218085 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20200310 MGI PMID:20709292 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20200310 MGI PMID:19218085 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0005074 impaired granulocyte bactericidal activity IAGP N RGD:5509061 20200310 MGI PMID:12649138 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20200310 MGI PMID:20709292 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20200310 MGI PMID:20709292 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20200310 MGI PMID:20709292 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:20709292 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:12649138 1332455 Pglyrp1 peptidoglycan recognition protein 1 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20200310 MGI PMID:20709292 1332458 Daglb diacylglycerol lipase, beta gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:20147530 1332458 Daglb diacylglycerol lipase, beta gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:21807615 1332458 Daglb diacylglycerol lipase, beta gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:20147530 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:17266133 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17266133 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:17266133 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:17266133 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17266133 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12904583 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17266133 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:17266133 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17266133 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17266133 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0004342 scapular bone foramen IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0004659 abnormal odontoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:17266133 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21059868 1332459 Mtf2 metal response element binding transcription factor 2 gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20180125 MGI PMID:17266133 1332461 Snap47 synaptosomal-associated protein, 47 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20211021 MGI 1332461 Snap47 synaptosomal-associated protein, 47 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150108 MGI 1332461 Snap47 synaptosomal-associated protein, 47 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1332461 Snap47 synaptosomal-associated protein, 47 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1332461 Snap47 synaptosomal-associated protein, 47 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20181227 MGI 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20181227 MGI 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210520 MGI 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0001147 small testis IEA N RGD:5509061 20210520 MGI 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23055941 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20181227 MGI 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23055941 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23055941 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0002981 increased liver weight IEA N RGD:5509061 20220519 MGI 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23055941 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:23055941 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1332463 Rabl2 RAB, member RAS oncogene family-like 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1332466 Pclaf PCNA clamp associated factor gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21844206 1332466 Pclaf PCNA clamp associated factor gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21844206 1332466 Pclaf PCNA clamp associated factor gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21844206 1332466 Pclaf PCNA clamp associated factor gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:21844206 1332466 Pclaf PCNA clamp associated factor gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21844206 1332466 Pclaf PCNA clamp associated factor gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:21844206 1332466 Pclaf PCNA clamp associated factor gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21844206 1332466 Pclaf PCNA clamp associated factor gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21844206 1332466 Pclaf PCNA clamp associated factor gene MP:0004974 decreased regulatory T cell number IEA N RGD:5509061 20201022 MGI 1332466 Pclaf PCNA clamp associated factor gene MP:0005018 decreased T cell number IEA N RGD:5509061 20201231 MGI 1332466 Pclaf PCNA clamp associated factor gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20201022 MGI 1332466 Pclaf PCNA clamp associated factor gene MP:0008124 decreased plasmacytoid dendritic cell number IEA N RGD:5509061 20201231 MGI 1332466 Pclaf PCNA clamp associated factor gene MP:0008126 increased dendritic cell number IEA N RGD:5509061 20201231 MGI 1332466 Pclaf PCNA clamp associated factor gene MP:0008127 decreased dendritic cell number IEA N RGD:5509061 20201231 MGI 1332466 Pclaf PCNA clamp associated factor gene MP:0008186 increased pro-B cell number IEA N RGD:5509061 20201231 MGI 1332466 Pclaf PCNA clamp associated factor gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21844206 1332466 Pclaf PCNA clamp associated factor gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21844206 1332466 Pclaf PCNA clamp associated factor gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21844206 1332466 Pclaf PCNA clamp associated factor gene MP:0013430 increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1332466 Pclaf PCNA clamp associated factor gene MP:0013649 decreased CD11b-high dendritic cell number IEA N RGD:5509061 20201231 MGI 1332466 Pclaf PCNA clamp associated factor gene MP:0013651 increased CD11b-low dendritic cell number IEA N RGD:5509061 20201231 MGI 1332466 Pclaf PCNA clamp associated factor gene MP:0013666 decreased immature NK cell number IEA N RGD:5509061 20201231 MGI 1332466 Pclaf PCNA clamp associated factor gene MP:0013673 increased mature NK cell number IEA N RGD:5509061 20201231 MGI 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0000420 ruffled hair IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0001406 abnormal gait IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20190502 MGI 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0002090 abnormal vision IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0002833 increased heart weight IEA N RGD:5509061 20200402 MGI 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0003786 premature aging IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0004222 iris synechia IEA N RGD:5509061 20240523 MGI 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20230601 MGI 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0012017 grizzled coat color IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0012065 increased astrocyte number IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332470 Taco1 translational activator of mitochondrially encoded cytochrome c oxidase I gene MP:0020434 increased astrocyte size IAGP N RGD:5509061 20170810 MGI PMID:27319982 1332476 Wdr83 WD repeat domain containing 83 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:19726548 1332476 Wdr83 WD repeat domain containing 83 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:19726548 1332476 Wdr83 WD repeat domain containing 83 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:19726548 1332476 Wdr83 WD repeat domain containing 83 gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:19726548 1332476 Wdr83 WD repeat domain containing 83 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:19726548 1332476 Wdr83 WD repeat domain containing 83 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:19726548 1332476 Wdr83 WD repeat domain containing 83 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19726548 1332476 Wdr83 WD repeat domain containing 83 gene MP:0011372 decreased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19726548 1332478 Heatr3 HEAT repeat containing 3 gene MP:0003443 increased circulating glycerol level IEA N RGD:5509061 20160804 MGI 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0000692 small spleen IEA N RGD:5509061 20200402 MGI 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:18165320 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18165320 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18165320 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:18165320 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18165320 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:18165320 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:18165320 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0004043 abnormal pH regulation IAGP N RGD:5509061 20141003 MGI PMID:18165320 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18165320 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20211021 MGI 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20160929 MGI PMID:27534441 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18165320 1332479 Slc4a10 solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1332480 Ak8 adenylate kinase 8 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:21746835 1332480 Ak8 adenylate kinase 8 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21746835 1332480 Ak8 adenylate kinase 8 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:21746835 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0000126 brittle teeth IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0000525 renal tubular acidosis IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0003017 decreased circulating bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0003017 decreased circulating bicarbonate level IAGP N RGD:5509061 20200310 MGI PMID:26224717 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0003030 acidemia IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0003031 acidosis IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0003031 acidosis IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0003267 constipation IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20200310 MGI PMID:26224717 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0005150 cachexia IAGP N RGD:5509061 20200310 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0005634 decreased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20200310 MGI PMID:26224717 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0009422 decreased gastrocnemius weight IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0009477 small cecum IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0009478 coiled cecum IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0009644 uremia IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0011736 decreased urine ammonia level IAGP N RGD:5509061 20200310 MGI PMID:26224717 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20170921 MGI PMID:21228764 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20200310 MGI PMID:26224717 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0014350 disorganized spleen B cell follicle IAGP N RGD:5509061 20240104 MGI PMID:17192275 1332483 Slc4a4 solute carrier family 4 (anion exchanger), member 4 gene MP:0030604 abnormal ammonia homeostasis IAGP N RGD:5509061 20200310 MGI PMID:26224717 1332485 Vars2 valyl-tRNA synthetase 2, mitochondrial gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20190502 MGI 1332485 Vars2 valyl-tRNA synthetase 2, mitochondrial gene MP:0003394 increased cardiac output IEA N RGD:5509061 20211021 MGI 1332485 Vars2 valyl-tRNA synthetase 2, mitochondrial gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332485 Vars2 valyl-tRNA synthetase 2, mitochondrial gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20211021 MGI 1332486 Sp7 Sp7 transcription factor 7 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16203988 1332486 Sp7 Sp7 transcription factor 7 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11792318 1332486 Sp7 Sp7 transcription factor 7 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16203988 1332486 Sp7 Sp7 transcription factor 7 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:11792318 1332486 Sp7 Sp7 transcription factor 7 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:16203988 1332486 Sp7 Sp7 transcription factor 7 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20221020 MGI PMID:34732852 1332486 Sp7 Sp7 transcription factor 7 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11792318 1332486 Sp7 Sp7 transcription factor 7 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11792318 1332486 Sp7 Sp7 transcription factor 7 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:11792318 1332486 Sp7 Sp7 transcription factor 7 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:16203988 1332486 Sp7 Sp7 transcription factor 7 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:22869368 1332486 Sp7 Sp7 transcription factor 7 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11792318 1332486 Sp7 Sp7 transcription factor 7 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16203988 1332486 Sp7 Sp7 transcription factor 7 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16203988 1332486 Sp7 Sp7 transcription factor 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170223 MGI PMID:27134141 1332486 Sp7 Sp7 transcription factor 7 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:11792318 1332486 Sp7 Sp7 transcription factor 7 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16203988 1332486 Sp7 Sp7 transcription factor 7 gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:22869368 1332486 Sp7 Sp7 transcription factor 7 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11792318 1332486 Sp7 Sp7 transcription factor 7 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16203988 1332486 Sp7 Sp7 transcription factor 7 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20221020 MGI PMID:34732852 1332486 Sp7 Sp7 transcription factor 7 gene MP:0008274 failure of bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22869368 1332486 Sp7 Sp7 transcription factor 7 gene MP:0008275 failure of endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22869368 1332486 Sp7 Sp7 transcription factor 7 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:16203988 1332486 Sp7 Sp7 transcription factor 7 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11792318 1332486 Sp7 Sp7 transcription factor 7 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16203988 1332487 Nyap1 neuronal tyrosine-phosphorylated phosphoinositide 3-kinase adaptor 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20180118 MGI PMID:21946561 1332487 Nyap1 neuronal tyrosine-phosphorylated phosphoinositide 3-kinase adaptor 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20180118 MGI PMID:21946561 1332487 Nyap1 neuronal tyrosine-phosphorylated phosphoinositide 3-kinase adaptor 1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20180118 MGI PMID:21946561 1332488 Zfp438 zinc finger protein 438 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1332491 Cfap36 cilia and flagella associated protein 36 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1332491 Cfap36 cilia and flagella associated protein 36 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1332491 Cfap36 cilia and flagella associated protein 36 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160804 MGI 1332492 Tmem131l transmembrane 131 like gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220519 MGI 1332492 Tmem131l transmembrane 131 like gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332494 Ccdc51 coiled-coil domain containing 51 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20191114 MGI PMID:31435016 1332494 Ccdc51 coiled-coil domain containing 51 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1332494 Ccdc51 coiled-coil domain containing 51 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20191114 MGI PMID:31435016 1332494 Ccdc51 coiled-coil domain containing 51 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1332497 Egfl7 EGF-like domain 7 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:17626061 1332497 Egfl7 EGF-like domain 7 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17626061 1332497 Egfl7 EGF-like domain 7 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17626061 1332497 Egfl7 EGF-like domain 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18987025 1332497 Egfl7 EGF-like domain 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9986727 1332497 Egfl7 EGF-like domain 7 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17626061 1332497 Egfl7 EGF-like domain 7 gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:17626061 1332497 Egfl7 EGF-like domain 7 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:17626061 1332497 Egfl7 EGF-like domain 7 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17626061 1332497 Egfl7 EGF-like domain 7 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17626061 1332498 Dlgap1 DLG associated protein 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20190502 MGI 1332498 Dlgap1 DLG associated protein 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20180913 MGI PMID:29396406 1332498 Dlgap1 DLG associated protein 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1332498 Dlgap1 DLG associated protein 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1332498 Dlgap1 DLG associated protein 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20180913 MGI PMID:29396406 1332498 Dlgap1 DLG associated protein 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20190502 MGI 1332498 Dlgap1 DLG associated protein 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20190502 MGI 1332498 Dlgap1 DLG associated protein 1 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20180913 MGI PMID:29396406 1332498 Dlgap1 DLG associated protein 1 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20190502 MGI 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20191219 MGI PMID:31661432 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0000601 small liver IEA N RGD:5509061 20170323 MGI 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20191219 MGI PMID:31661432 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:24487409 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0001577 anemia IEA N RGD:5509061 20170323 MGI 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0001790 abnormal immune system physiology IEA N RGD:5509061 20170323 MGI 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:24487409 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:24487409 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20170323 MGI 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:24487409 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:24487409 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24487409 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:24487409 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:24487409 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:24487409 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170323 MGI 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24487409 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:24487409 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20141003 MGI PMID:24487409 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20191219 MGI PMID:31661432 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:24487409 1332499 Glmp glycosylated lysosomal membrane protein gene MP:0031148 abnormal liver sinusoidal endothelial cell morphology IAGP N RGD:5509061 20201015 MGI PMID:31661432 1332500 Myod1 myogenic differentiation 1 gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:9609818 1332500 Myod1 myogenic differentiation 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:10694423 1332500 Myod1 myogenic differentiation 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9609818 1332500 Myod1 myogenic differentiation 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10694423 1332500 Myod1 myogenic differentiation 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:9609818 1332500 Myod1 myogenic differentiation 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:11060232 1332500 Myod1 myogenic differentiation 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:15386014 1332500 Myod1 myogenic differentiation 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:21212806 1332500 Myod1 myogenic differentiation 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:9609818 1332500 Myod1 myogenic differentiation 1 gene MP:0000730 increased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:17961534 1332500 Myod1 myogenic differentiation 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:10694423 1332500 Myod1 myogenic differentiation 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:14732408 1332500 Myod1 myogenic differentiation 1 gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10694423 1332500 Myod1 myogenic differentiation 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9609818 1332500 Myod1 myogenic differentiation 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9284044 1332500 Myod1 myogenic differentiation 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:9609818 1332500 Myod1 myogenic differentiation 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24239359 1332500 Myod1 myogenic differentiation 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24239359 1332500 Myod1 myogenic differentiation 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15386014 1332500 Myod1 myogenic differentiation 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9874799 1332500 Myod1 myogenic differentiation 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:17028574 1332500 Myod1 myogenic differentiation 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17028574 1332500 Myod1 myogenic differentiation 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11969267 1332500 Myod1 myogenic differentiation 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:1330322 1332500 Myod1 myogenic differentiation 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9609818 1332500 Myod1 myogenic differentiation 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:9874799 1332500 Myod1 myogenic differentiation 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:9874799 1332500 Myod1 myogenic differentiation 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9874799 1332500 Myod1 myogenic differentiation 1 gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:23933088 1332500 Myod1 myogenic differentiation 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:10694423 1332500 Myod1 myogenic differentiation 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:9874799 1332500 Myod1 myogenic differentiation 1 gene MP:0004846 absent skeletal muscle IAGP N RGD:5509061 20141003 MGI PMID:15386014 1332500 Myod1 myogenic differentiation 1 gene MP:0004846 absent skeletal muscle IAGP N RGD:5509061 20141003 MGI PMID:9609818 1332500 Myod1 myogenic differentiation 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9874799 1332500 Myod1 myogenic differentiation 1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9874799 1332500 Myod1 myogenic differentiation 1 gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:9874799 1332500 Myod1 myogenic differentiation 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21212806 1332500 Myod1 myogenic differentiation 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:9609818 1332500 Myod1 myogenic differentiation 1 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:9609818 1332500 Myod1 myogenic differentiation 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15386014 1332500 Myod1 myogenic differentiation 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10694423 1332500 Myod1 myogenic differentiation 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9609818 1332500 Myod1 myogenic differentiation 1 gene MP:0030957 abnormal myotube morphology IAGP N RGD:5509061 20190725 MGI PMID:11060232 1332500 Myod1 myogenic differentiation 1 gene MP:0031328 delayed skeletal muscle regeneration IAGP N RGD:5509061 20220106 MGI PMID:17028574 1332502 Slc46a3 solute carrier family 46, member 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210520 MGI 1332502 Slc46a3 solute carrier family 46, member 3 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20160421 MGI 1332502 Slc46a3 solute carrier family 46, member 3 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210520 MGI 1332502 Slc46a3 solute carrier family 46, member 3 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220519 MGI 1332502 Slc46a3 solute carrier family 46, member 3 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220519 MGI 1332502 Slc46a3 solute carrier family 46, member 3 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20210128 MGI 1332503 Abhd15 abhydrolase domain containing 15 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1332503 Abhd15 abhydrolase domain containing 15 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1332503 Abhd15 abhydrolase domain containing 15 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20211021 MGI 1332505 Unc119 unc-119 lipid binding chaperone gene MP:0000274 enlarged heart IEA N RGD:5509061 20210805 MGI 1332505 Unc119 unc-119 lipid binding chaperone gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210805 MGI 1332505 Unc119 unc-119 lipid binding chaperone gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17174953 1332505 Unc119 unc-119 lipid binding chaperone gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17174953 1332505 Unc119 unc-119 lipid binding chaperone gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17174953 1332505 Unc119 unc-119 lipid binding chaperone gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:17174953 1332505 Unc119 unc-119 lipid binding chaperone gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:17174953 1332505 Unc119 unc-119 lipid binding chaperone gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:17174953 1332506 Gins3 GINS complex subunit 3 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20230504 MGI PMID:35603789 1332506 Gins3 GINS complex subunit 3 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20230504 MGI PMID:35603789 1332506 Gins3 GINS complex subunit 3 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20230504 MGI PMID:35603789 1332506 Gins3 GINS complex subunit 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200514 MGI 1332506 Gins3 GINS complex subunit 3 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20230504 MGI PMID:35603789 1332506 Gins3 GINS complex subunit 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1332506 Gins3 GINS complex subunit 3 gene MP:0021086 decreased DNA replication IAGP N RGD:5509061 20230504 MGI PMID:35603789 1332509 Rpl3 ribosomal protein L3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230601 MGI PMID:37080962 1332510 Qrfpr pyroglutamylated RFamide peptide receptor gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16382160 1332510 Qrfpr pyroglutamylated RFamide peptide receptor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16382160 1332510 Qrfpr pyroglutamylated RFamide peptide receptor gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16382160 1332510 Qrfpr pyroglutamylated RFamide peptide receptor gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16382160 1332510 Qrfpr pyroglutamylated RFamide peptide receptor gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16382160 1332510 Qrfpr pyroglutamylated RFamide peptide receptor gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:16382160 1332510 Qrfpr pyroglutamylated RFamide peptide receptor gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:16382160 1332510 Qrfpr pyroglutamylated RFamide peptide receptor gene MP:0006392 abnormal nucleus pulposus morphology IAGP N RGD:5509061 20141003 MGI PMID:16382160 1332511 Sybu syntabulin (syntaxin-interacting) gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20201022 MGI 1332511 Sybu syntabulin (syntaxin-interacting) gene MP:0009709 hydrometra IEA N RGD:5509061 20201022 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0000599 enlarged liver IEA N RGD:5509061 20210826 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20230601 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20733033 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151126 MGI PMID:21779371 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20733033 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:20733033 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:21779371 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:20733033 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240627 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220519 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:21779371 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20733033 1332512 Padi4 peptidyl arginine deiminase, type IV gene MP:0020947 decreased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:21779371 1332513 Lsg1 large 60S subunit nuclear export GTPase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0001304 cataract IEA N RGD:5509061 20210520 MGI 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20201224 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0010613 abnormal mitral valve annulus morphology IAGP N RGD:5509061 20141003 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0010621 abnormal tricuspid valve annulus morphology IAGP N RGD:5509061 20141003 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24278323 1332514 Pdlim7 PDZ and LIM domain 7 gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20201224 MGI PMID:24278323 1332515 Zfp804a zinc finger protein 804A gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20240523 MGI 1332515 Zfp804a zinc finger protein 804A gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1332515 Zfp804a zinc finger protein 804A gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220519 MGI 1332515 Zfp804a zinc finger protein 804A gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210128 MGI 1332515 Zfp804a zinc finger protein 804A gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20220519 MGI 1332515 Zfp804a zinc finger protein 804A gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20211216 MGI PMID:33303946 1332515 Zfp804a zinc finger protein 804A gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20211216 MGI PMID:33303946 1332515 Zfp804a zinc finger protein 804A gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20211216 MGI PMID:33303946 1332515 Zfp804a zinc finger protein 804A gene MP:0009709 hydrometra IEA N RGD:5509061 20220519 MGI 1332515 Zfp804a zinc finger protein 804A gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20211216 MGI PMID:33303946 1332515 Zfp804a zinc finger protein 804A gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20211216 MGI PMID:33303946 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000111 cleft palate IEA N RGD:5509061 20210520 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:19767740 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:19767740 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20230601 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19767740 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19767740 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19877275 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000564 syndactyly IEA N RGD:5509061 20210520 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20141003 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:19877275 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19767740 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000927 small floor plate IAGP N RGD:5509061 20141003 MGI PMID:19877275 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19877275 1332516 Fuz fuzzy planar cell polarity protein gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:19877275 1332516 Fuz fuzzy planar cell polarity protein gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19767740 1332516 Fuz fuzzy planar cell polarity protein gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:19767740 1332516 Fuz fuzzy planar cell polarity protein gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19877275 1332516 Fuz fuzzy planar cell polarity protein gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:19877275 1332516 Fuz fuzzy planar cell polarity protein gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19877275 1332516 Fuz fuzzy planar cell polarity protein gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:19877275 1332516 Fuz fuzzy planar cell polarity protein gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:19877275 1332516 Fuz fuzzy planar cell polarity protein gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:19767740 1332516 Fuz fuzzy planar cell polarity protein gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20200514 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20200514 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20230601 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:19767740 1332516 Fuz fuzzy planar cell polarity protein gene MP:0003321 tracheoesophageal fistula IEA N RGD:5509061 20141003 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20230601 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:19877275 1332516 Fuz fuzzy planar cell polarity protein gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19767740 1332516 Fuz fuzzy planar cell polarity protein gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20220519 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0003817 abnormal pituitary diverticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0003924 diaphragmatic hernia IEA N RGD:5509061 20141003 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0004158 right aortic arch IEA N RGD:5509061 20141003 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:19767740 1332516 Fuz fuzzy planar cell polarity protein gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:19767740 1332516 Fuz fuzzy planar cell polarity protein gene MP:0006130 pulmonary valve atresia IEA N RGD:5509061 20141003 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0008480 absent eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:19877275 1332516 Fuz fuzzy planar cell polarity protein gene MP:0008797 facial cleft IEA N RGD:5509061 20220519 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:19767740 1332516 Fuz fuzzy planar cell polarity protein gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19877275 1332516 Fuz fuzzy planar cell polarity protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0011674 multiple major aortopulmonary collateral arteries IEA N RGD:5509061 20141003 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20141003 MGI 1332516 Fuz fuzzy planar cell polarity protein gene MP:0012260 encephalomeningocele IAGP N RGD:5509061 20141003 MGI PMID:19767740 1332516 Fuz fuzzy planar cell polarity protein gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:19767740 1332516 Fuz fuzzy planar cell polarity protein gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:19877275 1332516 Fuz fuzzy planar cell polarity protein gene MP:0013264 tongue ankylosis IAGP N RGD:5509061 20221027 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:19877275 1332516 Fuz fuzzy planar cell polarity protein gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20220721 MGI PMID:21935430 1332516 Fuz fuzzy planar cell polarity protein gene MP:0030373 Meckel's cartilage hyperplasia IAGP N RGD:5509061 20171207 MGI PMID:21935430 1332517 Atp5mk ATP synthase membrane subunit k gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20230720 MGI 1332517 Atp5mk ATP synthase membrane subunit k gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230720 MGI 1332517 Atp5mk ATP synthase membrane subunit k gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20230720 MGI 1332517 Atp5mk ATP synthase membrane subunit k gene MP:0001406 abnormal gait IEA N RGD:5509061 20230720 MGI 1332517 Atp5mk ATP synthase membrane subunit k gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20230720 MGI 1332517 Atp5mk ATP synthase membrane subunit k gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230720 MGI 1332517 Atp5mk ATP synthase membrane subunit k gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20230720 MGI 1332517 Atp5mk ATP synthase membrane subunit k gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230720 MGI 1332517 Atp5mk ATP synthase membrane subunit k gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230720 MGI 1332517 Atp5mk ATP synthase membrane subunit k gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230720 MGI 1332517 Atp5mk ATP synthase membrane subunit k gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230720 MGI 1332517 Atp5mk ATP synthase membrane subunit k gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20230720 MGI 1332517 Atp5mk ATP synthase membrane subunit k gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20230720 MGI 1332517 Atp5mk ATP synthase membrane subunit k gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20230720 MGI 1332524 Utp6 UTP6 small subunit processome component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1332525 Slc6a7 solute carrier family 6 (neurotransmitter transporter, L-proline), member 7 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20210422 MGI PMID:30177871 1332525 Slc6a7 solute carrier family 6 (neurotransmitter transporter, L-proline), member 7 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210520 MGI 1332525 Slc6a7 solute carrier family 6 (neurotransmitter transporter, L-proline), member 7 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20210422 MGI PMID:30177871 1332525 Slc6a7 solute carrier family 6 (neurotransmitter transporter, L-proline), member 7 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20210422 MGI PMID:30177871 1332525 Slc6a7 solute carrier family 6 (neurotransmitter transporter, L-proline), member 7 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20210422 MGI PMID:30177871 1332525 Slc6a7 solute carrier family 6 (neurotransmitter transporter, L-proline), member 7 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220519 MGI 1332525 Slc6a7 solute carrier family 6 (neurotransmitter transporter, L-proline), member 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1332525 Slc6a7 solute carrier family 6 (neurotransmitter transporter, L-proline), member 7 gene MP:0021088 impaired spatial memory extinction IAGP N RGD:5509061 20220310 MGI PMID:30177871 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20221110 MGI PMID:36196997 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0001147 small testis IAGP N RGD:5509061 20221110 MGI PMID:36196997 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20221110 MGI PMID:36196997 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20180308 MGI PMID:29088697 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20221110 MGI PMID:36196997 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20221110 MGI PMID:36196997 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20221110 MGI PMID:36196997 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20180308 MGI PMID:29088697 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20180308 MGI PMID:29088697 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20221110 MGI PMID:36196997 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20221110 MGI PMID:36196997 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20221110 MGI PMID:36196997 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20221110 MGI PMID:36196997 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0005187 abnormal penis morphology IAGP N RGD:5509061 20221110 MGI PMID:36196997 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0005188 small penis IAGP N RGD:5509061 20221110 MGI PMID:36196997 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20221110 MGI PMID:36196997 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0009104 small penile bone IAGP N RGD:5509061 20221110 MGI PMID:36196997 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:29088697 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:29088697 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20180308 MGI PMID:29088697 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20180308 MGI PMID:29088697 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20180308 MGI PMID:29088697 1332528 Kctd13 potassium channel tetramerisation domain containing 13 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:29088697 1332530 Arhgef9 CDC42 guanine nucleotide exchange factor 9 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17690689 1332530 Arhgef9 CDC42 guanine nucleotide exchange factor 9 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17690689 1332530 Arhgef9 CDC42 guanine nucleotide exchange factor 9 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17690689 1332530 Arhgef9 CDC42 guanine nucleotide exchange factor 9 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:17690689 1332530 Arhgef9 CDC42 guanine nucleotide exchange factor 9 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:17690689 1332530 Arhgef9 CDC42 guanine nucleotide exchange factor 9 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17690689 1332530 Arhgef9 CDC42 guanine nucleotide exchange factor 9 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18625319 1332530 Arhgef9 CDC42 guanine nucleotide exchange factor 9 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:17690689 1332530 Arhgef9 CDC42 guanine nucleotide exchange factor 9 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17690689 1332530 Arhgef9 CDC42 guanine nucleotide exchange factor 9 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17690689 1332530 Arhgef9 CDC42 guanine nucleotide exchange factor 9 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:17690689 1332531 Slc22a17 solute carrier family 22 (organic cation transporter), member 17 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1332531 Slc22a17 solute carrier family 22 (organic cation transporter), member 17 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1332531 Slc22a17 solute carrier family 22 (organic cation transporter), member 17 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1332531 Slc22a17 solute carrier family 22 (organic cation transporter), member 17 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332533 Selenos selenoprotein S gene MP:0000747 muscle weakness IAGP N RGD:5509061 20181220 MGI PMID:29668323 1332533 Selenos selenoprotein S gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20181220 MGI PMID:29668323 1332533 Selenos selenoprotein S gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20181220 MGI PMID:28592916 1332533 Selenos selenoprotein S gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20181220 MGI PMID:28592916 1332533 Selenos selenoprotein S gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20181220 MGI PMID:28592916 1332533 Selenos selenoprotein S gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20181220 MGI PMID:28592916 1332533 Selenos selenoprotein S gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20181220 MGI PMID:28592916 1332533 Selenos selenoprotein S gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20181220 MGI PMID:28592916 1332534 Fbxw9 F-box and WD-40 domain protein 9 gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20170105 MGI 1332534 Fbxw9 F-box and WD-40 domain protein 9 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20160811 MGI 1332534 Fbxw9 F-box and WD-40 domain protein 9 gene MP:0000690 absent spleen IEA N RGD:5509061 20170105 MGI 1332534 Fbxw9 F-box and WD-40 domain protein 9 gene MP:0001293 anophthalmia IEA N RGD:5509061 20170105 MGI 1332534 Fbxw9 F-box and WD-40 domain protein 9 gene MP:0002282 abnormal trachea morphology IEA N RGD:5509061 20170105 MGI 1332534 Fbxw9 F-box and WD-40 domain protein 9 gene MP:0008024 absent lymph nodes IEA N RGD:5509061 20170105 MGI 1332534 Fbxw9 F-box and WD-40 domain protein 9 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1332534 Fbxw9 F-box and WD-40 domain protein 9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1332534 Fbxw9 F-box and WD-40 domain protein 9 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1332535 Adam32 a disintegrin and metallopeptidase domain 32 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20201022 MGI 1332535 Adam32 a disintegrin and metallopeptidase domain 32 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 1332535 Adam32 a disintegrin and metallopeptidase domain 32 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20181227 MGI 1332535 Adam32 a disintegrin and metallopeptidase domain 32 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20181227 MGI 1332535 Adam32 a disintegrin and metallopeptidase domain 32 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 1332539 U2surp U2 snRNP-associated SURP domain containing gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220811 MGI 1332539 U2surp U2 snRNP-associated SURP domain containing gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1332539 U2surp U2 snRNP-associated SURP domain containing gene MP:0002608 increased hematocrit IEA N RGD:5509061 20220811 MGI 1332539 U2surp U2 snRNP-associated SURP domain containing gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20231207 MGI 1332539 U2surp U2 snRNP-associated SURP domain containing gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230601 MGI 1332539 U2surp U2 snRNP-associated SURP domain containing gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1332541 Jhy junctional cadherin complex regulator gene MP:0000440 domed cranium IAGP N RGD:5509061 20160922 MGI PMID:23906841 1332541 Jhy junctional cadherin complex regulator gene MP:0001263 weight loss IAGP N RGD:5509061 20160922 MGI PMID:23906841 1332541 Jhy junctional cadherin complex regulator gene MP:0001393 ataxia IAGP N RGD:5509061 20160922 MGI PMID:23906841 1332541 Jhy junctional cadherin complex regulator gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20160922 MGI PMID:23906841 1332541 Jhy junctional cadherin complex regulator gene MP:0002083 premature death IAGP N RGD:5509061 20160922 MGI PMID:23906841 1332541 Jhy junctional cadherin complex regulator gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20160922 MGI PMID:23906841 1332541 Jhy junctional cadherin complex regulator gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20160922 MGI PMID:23906841 1332541 Jhy junctional cadherin complex regulator gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20160922 MGI PMID:23906841 1332541 Jhy junctional cadherin complex regulator gene MP:0030963 abnormal brain ependyma motile cilium location or orientation IAGP N RGD:5509061 20190725 MGI PMID:23906841 1332541 Jhy junctional cadherin complex regulator gene MP:0030964 decreased brain ependyma motile cilium length IAGP N RGD:5509061 20190725 MGI PMID:23906841 1332541 Jhy junctional cadherin complex regulator gene MP:0030966 decreased brain ependyma motile cilium number IAGP N RGD:5509061 20190725 MGI PMID:23906841 1332542 Gtsf1 gametocyte specific factor 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19735653 1332542 Gtsf1 gametocyte specific factor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19735653 1332542 Gtsf1 gametocyte specific factor 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19735653 1332542 Gtsf1 gametocyte specific factor 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19735653 1332542 Gtsf1 gametocyte specific factor 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:19735653 1332542 Gtsf1 gametocyte specific factor 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:19735653 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20170921 MGI PMID:28294127 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18059270 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20170921 MGI PMID:28294127 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18059270 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20170921 MGI PMID:28294127 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20240516 MGI PMID:36803766 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20211021 MGI 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20240516 MGI PMID:36803766 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19843959 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0004867 decreased platelet calcium level IAGP N RGD:5509061 20141003 MGI PMID:18952890 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20170921 MGI PMID:28294127 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20240516 MGI PMID:36803766 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18059270 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:18952890 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20170921 MGI PMID:28294127 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20170921 MGI PMID:28294127 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20170921 MGI PMID:28294127 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20240516 MGI PMID:36803766 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18059270 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:18059270 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0009257 dilated seminiferous tubule IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0009817 decreased leukotriene level IAGP N RGD:5509061 20141003 MGI PMID:18059270 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0010183 abnormal CD4-positive helper T cell morphology IAGP N RGD:5509061 20170921 MGI PMID:28294127 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18952890 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18591248 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0020355 abnormal Sertoli cell barrier morphology IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332545 Orai1 ORAI calcium release-activated calcium modulator 1 gene MP:0031389 abnormal ectoplasmic specialization morphology IAGP N RGD:5509061 20220519 MGI PMID:26969191 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:20106865 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:20106865 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:20106865 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20308544 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20308544 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20308544 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:20106865 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20308544 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20308544 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20308544 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20106865 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20106865 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0011705 absent fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:17476360 1332546 Pggt1b protein geranylgeranyltransferase type I, beta subunit gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:20308544 1332547 Kat7 K(lysine) acetyltransferase 7 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21149574 1332547 Kat7 K(lysine) acetyltransferase 7 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:21149574 1332547 Kat7 K(lysine) acetyltransferase 7 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:21149574 1332547 Kat7 K(lysine) acetyltransferase 7 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:21149574 1332547 Kat7 K(lysine) acetyltransferase 7 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:21149574 1332547 Kat7 K(lysine) acetyltransferase 7 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:21149574 1332547 Kat7 K(lysine) acetyltransferase 7 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21149574 1332547 Kat7 K(lysine) acetyltransferase 7 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:21149574 1332547 Kat7 K(lysine) acetyltransferase 7 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:21149574 1332547 Kat7 K(lysine) acetyltransferase 7 gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:21149574 1332547 Kat7 K(lysine) acetyltransferase 7 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:21149574 1332547 Kat7 K(lysine) acetyltransferase 7 gene MP:0010355 abnormal first pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21149574 1332547 Kat7 K(lysine) acetyltransferase 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21149574 1332547 Kat7 K(lysine) acetyltransferase 7 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:21149574 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:21467224 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0000836 abnormal substantia nigra morphology IAGP N RGD:5509061 20210114 MGI PMID:32439544 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001258 decreased body length IEA N RGD:5509061 20170420 MGI 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22087241 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20210114 MGI PMID:32439544 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17018277 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210114 MGI PMID:32439544 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20200220 MGI PMID:29925537 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002083 premature death IAGP N RGD:5509061 20191107 MGI PMID:30346946 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20210114 MGI PMID:32439544 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:24280126 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:16775082 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002899 fatigue IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20170420 MGI 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20170420 MGI 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:17018277 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22087241 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200220 MGI PMID:29925537 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21467224 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0003916 decreased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0003917 increased kidney weight IEA N RGD:5509061 20170420 MGI 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:24280126 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:17018277 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:16775082 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:21467224 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0004955 increased thymus weight IEA N RGD:5509061 20170420 MGI 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:16775082 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005156 bradykinesia IAGP N RGD:5509061 20210114 MGI PMID:32439544 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20170420 MGI 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20200220 MGI PMID:29925537 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20200220 MGI PMID:29925537 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:24280126 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:24280126 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:24280126 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:24280126 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16122419 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:16775082 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20160929 MGI PMID:27622213 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:24280126 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20200220 MGI PMID:29925537 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:16775082 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0006237 abnormal choroid vasculature morphology IAGP N RGD:5509061 20200220 MGI PMID:29925537 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0006238 abnormal choriocapillaris morphology IAGP N RGD:5509061 20200220 MGI PMID:29925537 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20160414 MGI PMID:21467224 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200220 MGI PMID:29925537 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20200220 MGI PMID:29925537 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200220 MGI PMID:29925537 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0008834 abnormal melanosome transport IAGP N RGD:5509061 20200220 MGI PMID:29925537 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20200220 MGI PMID:29925537 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22087241 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22087241 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22087241 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0009305 decreased retroperitoneal fat pad weight IEA N RGD:5509061 20170420 MGI 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0009422 decreased gastrocnemius weight IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0009426 decreased soleus weight IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16122419 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0009710 anhedonia IAGP N RGD:5509061 20141204 MGI PMID:25259918 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22087241 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20170420 MGI 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:24280126 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:15760270 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15454086 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18628400 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20160929 MGI PMID:27622213 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20191107 MGI PMID:30346946 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20200220 MGI PMID:29925537 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:17932564 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0013307 increased adrenal gland weight IEA N RGD:5509061 20170420 MGI 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0013894 abnormal behavioral response to amphetamine IAGP N RGD:5509061 20160929 MGI PMID:27622213 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0014143 decreased body fat mass IEA N RGD:5509061 20170420 MGI 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0020038 retina macular degeneration IAGP N RGD:5509061 20200220 MGI PMID:29925537 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0020875 decreased nervous system dopamine level IAGP N RGD:5509061 20210114 MGI PMID:32439544 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200220 MGI PMID:29925537 1332548 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15760270 1332551 Tlcd3b TLC domain containing 3B gene MP:0001258 decreased body length IEA N RGD:5509061 20230601 MGI 1332551 Tlcd3b TLC domain containing 3B gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1332551 Tlcd3b TLC domain containing 3B gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20201022 MGI 1332551 Tlcd3b TLC domain containing 3B gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1332551 Tlcd3b TLC domain containing 3B gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20220519 MGI PMID:33077892 1332551 Tlcd3b TLC domain containing 3B gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20220519 MGI PMID:33077892 1332551 Tlcd3b TLC domain containing 3B gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20220519 MGI PMID:33077892 1332551 Tlcd3b TLC domain containing 3B gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20201022 MGI 1332551 Tlcd3b TLC domain containing 3B gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 1332551 Tlcd3b TLC domain containing 3B gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20220519 MGI PMID:33077892 1332552 Klrc1 killer cell lectin-like receptor subfamily C, member 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20160317 MGI PMID:25251060 1332552 Klrc1 killer cell lectin-like receptor subfamily C, member 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20160317 MGI PMID:25251060 1332552 Klrc1 killer cell lectin-like receptor subfamily C, member 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20160317 MGI PMID:25251060 1332552 Klrc1 killer cell lectin-like receptor subfamily C, member 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20160317 MGI PMID:25251060 1332552 Klrc1 killer cell lectin-like receptor subfamily C, member 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20160317 MGI PMID:25251060 1332552 Klrc1 killer cell lectin-like receptor subfamily C, member 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20160317 MGI PMID:25251060 1332552 Klrc1 killer cell lectin-like receptor subfamily C, member 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20160317 MGI PMID:25251060 1332552 Klrc1 killer cell lectin-like receptor subfamily C, member 1 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20160317 MGI PMID:25251060 1332552 Klrc1 killer cell lectin-like receptor subfamily C, member 1 gene MP:0020931 increased susceptibility to Adenoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:25251060 1332552 Klrc1 killer cell lectin-like receptor subfamily C, member 1 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:25251060 1332559 Gpr151 G protein-coupled receptor 151 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20190606 MGI PMID:30395363 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20190606 MGI PMID:30395363 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0003198 calcified tendon IAGP N RGD:5509061 20190606 MGI PMID:30395363 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20201022 MGI 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20190606 MGI PMID:30395363 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20190606 MGI PMID:30395363 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20190606 MGI PMID:30395363 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20210128 MGI 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0009877 exostosis IAGP N RGD:5509061 20190606 MGI PMID:30395363 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0010313 increased osteoma incidence IAGP N RGD:5509061 20190606 MGI PMID:30395363 1332560 Cibar1 CBY1 interacting BAR domain containing 1 gene MP:0013304 osteophytes IAGP N RGD:5509061 20190606 MGI PMID:30395363 1332561 Gkn2 gastrokine 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1332561 Gkn2 gastrokine 2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332561 Gkn2 gastrokine 2 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332561 Gkn2 gastrokine 2 gene MP:0002175 decreased brain weight IEA N RGD:5509061 20211021 MGI 1332561 Gkn2 gastrokine 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332561 Gkn2 gastrokine 2 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332561 Gkn2 gastrokine 2 gene MP:0002544 brachydactyly IEA N RGD:5509061 20210826 MGI 1332561 Gkn2 gastrokine 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220519 MGI 1332561 Gkn2 gastrokine 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1332561 Gkn2 gastrokine 2 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332561 Gkn2 gastrokine 2 gene MP:0005211 increased stomach mucosa thickness IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332561 Gkn2 gastrokine 2 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332561 Gkn2 gastrokine 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332561 Gkn2 gastrokine 2 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332561 Gkn2 gastrokine 2 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332561 Gkn2 gastrokine 2 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332561 Gkn2 gastrokine 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1332561 Gkn2 gastrokine 2 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332561 Gkn2 gastrokine 2 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332561 Gkn2 gastrokine 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20220519 MGI 1332561 Gkn2 gastrokine 2 gene MP:0013567 gastric gland atrophy IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332561 Gkn2 gastrokine 2 gene MP:0013662 decreased myeloid cell number IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332561 Gkn2 gastrokine 2 gene MP:0020186 abnormal susceptibility to bacterial infection IAGP N RGD:5509061 20170608 MGI PMID:26974160 1332562 Tbc1d23 TBC1 domain family, member 23 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22312129 1332562 Tbc1d23 TBC1 domain family, member 23 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22312129 1332562 Tbc1d23 TBC1 domain family, member 23 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:22312129 1332562 Tbc1d23 TBC1 domain family, member 23 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22312129 1332565 Rps18 ribosomal protein S18 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9784405 1332566 Enah ENAH actin regulator gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10069337 1332566 Enah ENAH actin regulator gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332566 Enah ENAH actin regulator gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:10069337 1332566 Enah ENAH actin regulator gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10069337 1332566 Enah ENAH actin regulator gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10069337 1332566 Enah ENAH actin regulator gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10069337 1332566 Enah ENAH actin regulator gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:10069337 1332566 Enah ENAH actin regulator gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332566 Enah ENAH actin regulator gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332566 Enah ENAH actin regulator gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332566 Enah ENAH actin regulator gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:10069337 1332566 Enah ENAH actin regulator gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:10069337 1332566 Enah ENAH actin regulator gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:10069337 1332566 Enah ENAH actin regulator gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:22908313 1332566 Enah ENAH actin regulator gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332566 Enah ENAH actin regulator gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332566 Enah ENAH actin regulator gene MP:0008129 absent brain internal capsule IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332566 Enah ENAH actin regulator gene MP:0008221 abnormal hippocampal commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:10069337 1332566 Enah ENAH actin regulator gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332566 Enah ENAH actin regulator gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332566 Enah ENAH actin regulator gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332566 Enah ENAH actin regulator gene MP:0009026 abnormal brain pia mater morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332566 Enah ENAH actin regulator gene MP:0009027 abnormal subarachnoid space morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332566 Enah ENAH actin regulator gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10069337 1332566 Enah ENAH actin regulator gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332566 Enah ENAH actin regulator gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332566 Enah ENAH actin regulator gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332566 Enah ENAH actin regulator gene MP:0011724 ectopic cortical neuron IAGP N RGD:5509061 20141003 MGI PMID:17988629 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:22539352 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:22539352 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22539352 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22539352 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22896338 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22896338 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22896338 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:22539352 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:22896338 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22896338 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:22896338 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:22896338 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:22539352 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22896338 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22896338 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22896338 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:22539352 1332567 Uimc1 ubiquitin interaction motif containing 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:22896338 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0001539 decreased caudal vertebrae number IEA N RGD:5509061 20141003 MGI 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:21085614 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0003345 decreased rib number IEA N RGD:5509061 20160804 MGI 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20160804 MGI 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0004648 decreased thoracic vertebrae number IEA N RGD:5509061 20160804 MGI 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:21085614 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22101742 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160804 MGI 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20160804 MGI 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160804 MGI 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20141003 MGI 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22101742 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:21085614 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:21085614 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21085614 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:21085614 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:22101742 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21085614 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:21085614 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:21085614 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:21085614 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21085614 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18704116 1332569 Dusp4 dual specificity phosphatase 4 gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20141003 MGI 1332570 Zfp414 zinc finger protein 414 gene MP:0000433 microcephaly IEA N RGD:5509061 20221215 MGI 1332570 Zfp414 zinc finger protein 414 gene MP:0001293 anophthalmia IEA N RGD:5509061 20221215 MGI 1332570 Zfp414 zinc finger protein 414 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20221215 MGI 1332570 Zfp414 zinc finger protein 414 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20221215 MGI 1332570 Zfp414 zinc finger protein 414 gene MP:0011496 abnormal head size IEA N RGD:5509061 20221215 MGI 1332571 Smg8 SMG8 nonsense mediated mRNA decay factor gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1332573 Gja10 gap junction protein, alpha 10 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22855819 1332573 Gja10 gap junction protein, alpha 10 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22855819 1332573 Gja10 gap junction protein, alpha 10 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1332573 Gja10 gap junction protein, alpha 10 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20210128 MGI 1332573 Gja10 gap junction protein, alpha 10 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:22855819 1332573 Gja10 gap junction protein, alpha 10 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1332573 Gja10 gap junction protein, alpha 10 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:22855819 1332573 Gja10 gap junction protein, alpha 10 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1332573 Gja10 gap junction protein, alpha 10 gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:24349437 1332573 Gja10 gap junction protein, alpha 10 gene MP:0004727 absent epididymis IEA N RGD:5509061 20210128 MGI 1332573 Gja10 gap junction protein, alpha 10 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:24349437 1332573 Gja10 gap junction protein, alpha 10 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16820008 1332573 Gja10 gap junction protein, alpha 10 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22855819 1332573 Gja10 gap junction protein, alpha 10 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16820008 1332573 Gja10 gap junction protein, alpha 10 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18320035 1332573 Gja10 gap junction protein, alpha 10 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20230413 MGI PMID:35169021 1332573 Gja10 gap junction protein, alpha 10 gene MP:0006415 absent testes IEA N RGD:5509061 20210128 MGI 1332573 Gja10 gap junction protein, alpha 10 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22855819 1332573 Gja10 gap junction protein, alpha 10 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:22855819 1332573 Gja10 gap junction protein, alpha 10 gene MP:0008520 disorganized retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:22855819 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:19584095 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20201217 MGI PMID:31098411 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0002626 increased heart rate IAGP N RGD:5509061 20210916 MGI PMID:28630914 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0002713 abnormal glycogen catabolism IAGP N RGD:5509061 20201217 MGI PMID:31098411 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20210916 MGI PMID:28630914 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:19584095 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20201217 MGI PMID:31098411 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20201217 MGI PMID:31098411 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20210916 MGI PMID:28630914 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20210916 MGI PMID:28630914 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20201217 MGI PMID:31098411 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20210916 MGI PMID:28630914 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20201217 MGI PMID:31098411 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20201217 MGI PMID:31098411 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:19584095 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20210916 MGI PMID:28630914 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20201217 MGI PMID:31098411 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0012655 increased catalase level IAGP N RGD:5509061 20201217 MGI PMID:31098411 1332578 Obscn obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF gene MP:0031635 increased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:28630914 1332579 Cnppd1 cyclin Pas1/PHO80 domain containing 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1332579 Cnppd1 cyclin Pas1/PHO80 domain containing 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0000601 small liver IEA N RGD:5509061 20220519 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:23007167 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20220811 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220811 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001148 enlarged testis IEA N RGD:5509061 20220811 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:18923670 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18923670 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170216 MGI PMID:26291320 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:18212115 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001356 increased aggression towards female mice IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:18212115 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18212115 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001375 abnormal mating preference IAGP N RGD:5509061 20141003 MGI PMID:21441904 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20230601 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22419158 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20231207 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20220811 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23007167 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220811 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:22419158 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220811 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220811 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20220519 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170216 MGI PMID:26291320 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23467366 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:18923670 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0003064 decreased coping response IAGP N RGD:5509061 20141003 MGI PMID:18212115 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0003064 decreased coping response IAGP N RGD:5509061 20141003 MGI PMID:23467366 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20220811 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20220811 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:18923670 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0003877 abnormal serotonergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18665319 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:18923670 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20220811 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20220811 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0005238 increased brain size IEA N RGD:5509061 20220519 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:15247473 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18923670 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0005655 increased aggression IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0006276 abnormal autonomic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0008845 abnormal paraventricular hypothalamic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:23007167 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0008847 abnormal suprachiasmatic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:23007167 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:20722968 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:21441904 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:22419158 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20170216 MGI PMID:26291320 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:18212115 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:18923670 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0011016 increased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:20722968 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0011021 abnormal circadian regulation of heart rate IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0011022 abnormal circadian regulation of systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:19520831 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23007167 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170216 MGI PMID:26291320 1332580 Tph2 tryptophan hydroxylase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1332581 Septin9 septin 9 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23644740 1332581 Septin9 septin 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21824004 1332581 Septin9 septin 9 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23644740 1332581 Septin9 septin 9 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23644740 1332581 Septin9 septin 9 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:23644740 1332581 Septin9 septin 9 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23644740 1332581 Septin9 septin 9 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21824004 1332581 Septin9 septin 9 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23644740 1332581 Septin9 septin 9 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23644740 1332581 Septin9 septin 9 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23644740 1332581 Septin9 septin 9 gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23644740 1332581 Septin9 septin 9 gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23644740 1332581 Septin9 septin 9 gene MP:0010836 decreased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23644740 1332581 Septin9 septin 9 gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23644740 1332581 Septin9 septin 9 gene MP:0010839 decreased CD8-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23644740 1332581 Septin9 septin 9 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21824004 1357431 Cia27_m collagen induced arthritis 27 (mouse) qtl MP:0002493 increased IgG level IAGP N RGD:5509061 20111116 MGI PMID:15529344 1357431 Cia27_m collagen induced arthritis 27 (mouse) qtl MP:0002493 increased IgG level IAGP N RGD:5509061 20111116 MGI PMID:17082620 1357431 Cia27_m collagen induced arthritis 27 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15529344 1357431 Cia27_m collagen induced arthritis 27 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15529344 1357432 Hdlcl1_m HDL cholesterol level 1 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:15514201 1357432 Hdlcl1_m HDL cholesterol level 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15514201 1357433 Dbts2_m diabetes 2 (mouse) qtl MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357433 Dbts2_m diabetes 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357434 Obsty1_m obesity 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357434 Obsty1_m obesity 1 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357434 Obsty1_m obesity 1 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357434 Obsty1_m obesity 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357434 Obsty1_m obesity 1 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357434 Obsty1_m obesity 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357434 Obsty1_m obesity 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357434 Obsty1_m obesity 1 (mouse) qtl MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357434 Obsty1_m obesity 1 (mouse) qtl MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357434 Obsty1_m obesity 1 (mouse) qtl MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357434 Obsty1_m obesity 1 (mouse) qtl MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357435 Epfq2_m epididymal fat pad weight QTL 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357435 Epfq2_m epididymal fat pad weight QTL 2 (mouse) qtl MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357435 Epfq2_m epididymal fat pad weight QTL 2 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357436 Splq1_m spleen weight QTL 1 (mouse) qtl MP:0004953 decreased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357436 Splq1_m spleen weight QTL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357436 Splq1_m spleen weight QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357437 Epfq4_m epididymal fat pad weight QTL 4 (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357437 Epfq4_m epididymal fat pad weight QTL 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357438 Pwatq1_m percent water in carcass QTL 1 (mouse) qtl MP:0000683 decreased percent water in carcass IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357438 Pwatq1_m percent water in carcass QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357438 Pwatq1_m percent water in carcass QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15058381 1357439 Popoa_m premature ovulation and primary oocyte arrest (mouse) qtl MP:0001928 abnormal ovulation IAGP N RGD:5509061 20111116 MGI PMID:15509702 1357439 Popoa_m premature ovulation and primary oocyte arrest (mouse) qtl MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20111116 MGI PMID:15509702 1357439 Popoa_m premature ovulation and primary oocyte arrest (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20240510 MGI Created by mouse qtl pipeline PMID:15509702 1357439 Popoa_m premature ovulation and primary oocyte arrest (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15509702 1357440 Hrtpq1_m heart weight percentage QTL 1 (mouse) qtl MP:0002833 increased heart weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357440 Hrtpq1_m heart weight percentage QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15058381 1357440 Hrtpq1_m heart weight percentage QTL 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357441 Epfq3_m epididymal fat pad weight QTL 3 (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357441 Epfq3_m epididymal fat pad weight QTL 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357442 Dbts1_m diabetes 1 (mouse) qtl MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357442 Dbts1_m diabetes 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357443 Lhyp_m lung hyperpermeability (mouse) qtl MP:0002295 abnormal pulmonary circulation IAGP N RGD:5509061 20111116 MGI PMID:10783135 1357443 Lhyp_m lung hyperpermeability (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10783135 1357443 Lhyp_m lung hyperpermeability (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10783135 1357444 Hdl35_m HDL level 35 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:9077551 1357444 Hdl35_m HDL level 35 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9077551 1357447 Heal13_m wound healing/regeneration 13 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:15225218 1357447 Heal13_m wound healing/regeneration 13 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15225218 1357448 Bdywt_m body weight (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15514201 1357448 Bdywt_m body weight (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15514201 1357449 Hcs6_m hepatocarcinogenesis susceptibility 6 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7829059 1357449 Hcs6_m hepatocarcinogenesis susceptibility 6 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:7829059 1357449 Hcs6_m hepatocarcinogenesis susceptibility 6 (mouse) qtl MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20111116 MGI PMID:7829059 1357450 Szs7_m seizure susceptibility 7 (mouse) qtl MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20111116 MGI PMID:11472065 1357450 Szs7_m seizure susceptibility 7 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1357450 Szs7_m seizure susceptibility 7 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11472065 1357452 Vtbt18_m vertebral trabecular bone trait 18 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357452 Vtbt18_m vertebral trabecular bone trait 18 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357453 Kidq4_m kidney weight QTL 4 (mouse) qtl MP:0003918 decreased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357453 Kidq4_m kidney weight QTL 4 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357454 Kidq1_m kidney weight QTL 1 (mouse) qtl MP:0003918 decreased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357454 Kidq1_m kidney weight QTL 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357455 Trmq4_m T cell ratio modifier QTL 4 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:15611280 1357455 Trmq4_m T cell ratio modifier QTL 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15611280 1357455 Trmq4_m T cell ratio modifier QTL 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15611280 1357456 Hdl37_m HDL level 37 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:9077551 1357456 Hdl37_m HDL level 37 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9077551 1357459 Nhdlq7_m non-HDL QTL 7 (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:15210844 1357459 Nhdlq7_m non-HDL QTL 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15210844 1357460 Vtbt4_m vertebral trabecular bone trait 4 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357460 Vtbt4_m vertebral trabecular bone trait 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357461 Idd2_m insulin dependent diabetes susceptibility 2 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:7552995 1357461 Idd2_m insulin dependent diabetes susceptibility 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:2576007|PMID:7578887|PMID:7556956 1357461 Idd2_m insulin dependent diabetes susceptibility 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:2576007|PMID:7578887|PMID:7556956 1357461 Idd2_m insulin dependent diabetes susceptibility 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:2576007|PMID:7578887|PMID:7556956 1357461 Idd2_m insulin dependent diabetes susceptibility 2 (mouse) qtl MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20111116 MGI PMID:7578887 1357462 Hlbsb1_m hepatic lipase activity in BSB 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15314098 1357462 Hlbsb1_m hepatic lipase activity in BSB 1 (mouse) qtl MP:0011581 increased triglyceride lipase activity IAGP N RGD:5509061 20120209 MGI PMID:15314098 1357463 Vtbt14_m vertebral trabecular bone trait 14 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357463 Vtbt14_m vertebral trabecular bone trait 14 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357465 Vtbt6_m vertebral trabecular bone trait 6 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357465 Vtbt6_m vertebral trabecular bone trait 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357467 Arigg4_m anti-RBC IgG antibodies 4 (mouse) qtl MP:0004797 increased anti-erythrocyte antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357467 Arigg4_m anti-RBC IgG antibodies 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357468 Rplag_m reduced platelet aggregation (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14739220 1357468 Rplag_m reduced platelet aggregation (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14739220 1357468 Rplag_m reduced platelet aggregation (mouse) qtl MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20111116 MGI PMID:14739220 1357469 Kidq5_m kidney weight QTL 5 (mouse) qtl MP:0003918 decreased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357469 Kidq5_m kidney weight QTL 5 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357470 Obq16_m obesity QTL 16 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15210844 1357470 Obq16_m obesity QTL 16 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15210844 1357470 Obq16_m obesity QTL 16 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:15210844 1357470 Obq16_m obesity QTL 16 (mouse) qtl MP:0006087 increased body mass index IAGP N RGD:5509061 20111116 MGI PMID:15210844 1357471 Arigg10_m anti-RBC IgG antibodies 10 (mouse) qtl MP:0004797 increased anti-erythrocyte antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357471 Arigg10_m anti-RBC IgG antibodies 10 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357472 Lmblgq6_m limb length QTL 6 (mouse) qtl MP:0004348 long femur IAGP N RGD:5509061 20111116 MGI PMID:12118102 1357472 Lmblgq6_m limb length QTL 6 (mouse) qtl MP:0004350 long humerus IAGP N RGD:5509061 20111116 MGI PMID:12118102 1357472 Lmblgq6_m limb length QTL 6 (mouse) qtl MP:0004357 long tibia IAGP N RGD:5509061 20111116 MGI PMID:12118102 1357472 Lmblgq6_m limb length QTL 6 (mouse) qtl MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20111116 MGI PMID:12118102 1357472 Lmblgq6_m limb length QTL 6 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1357472 Lmblgq6_m limb length QTL 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1357475 w3q13_m weight 3 weeks QTL 13 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1357475 w3q13_m weight 3 weeks QTL 13 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1357476 Mdmsc4_m modifier of muscularity 4 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:14504233 1357476 Mdmsc4_m modifier of muscularity 4 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14504233 1357477 Lgdr2_m liver Gapd decay rate 2 (mouse) qtl MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20111116 MGI PMID:15519297 1357477 Lgdr2_m liver Gapd decay rate 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15519297 1357478 Kdnw1_m kidney weight 1 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357478 Kdnw1_m kidney weight 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357478 Kdnw1_m kidney weight 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15561968 1357479 Splwt1_m spleen weight 1 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357479 Splwt1_m spleen weight 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15561968 1357479 Splwt1_m spleen weight 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357479 Splwt1_m spleen weight 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357480 Igf1sl4_m IGF-1 serum levels 4 (mouse) qtl MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:11033447 1357480 Igf1sl4_m IGF-1 serum levels 4 (mouse) qtl MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20201002 MGI PMID:11033447 1357480 Igf1sl4_m IGF-1 serum levels 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11033447 1357480 Igf1sl4_m IGF-1 serum levels 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11033447 1357481 Aaj2_m anxiety in A/J 2 (mouse) qtl MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:15371360 1357481 Aaj2_m anxiety in A/J 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15371360 1357482 Nhdlq4_m non-HDL QTL 4 (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:15210844 1357482 Nhdlq4_m non-HDL QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15210844 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0001258 decreased body length IAGP N RGD:5509061 20111116 MGI PMID:17536020 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:15181537 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:15181537 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:17536020 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15181537 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15181537 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15181537 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15181537 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0005449 abnormal food intake IAGP N RGD:5509061 20111116 MGI PMID:17536020 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20111116 MGI PMID:17536020 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:15166164 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:17536020 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15181537 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15181537 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:15166164 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:15181537 1357484 Bsbob_m BSB obesity (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:17536020 1357485 Lgq4_m late growth QTL 4 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 1357485 Lgq4_m late growth QTL 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1357486 Bmch2_m bone mechanical trait 2 (mouse) qtl MP:0001542 abnormal bone strength IAGP N RGD:5509061 20111116 MGI PMID:15312250 1357486 Bmch2_m bone mechanical trait 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15312250 1357487 ecs_m epistatic circling SWR/J (mouse) qtl MP:0001394 circling IAGP N RGD:5509061 20111116 MGI PMID:11932245 1357487 ecs_m epistatic circling SWR/J (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 1357487 ecs_m epistatic circling SWR/J (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20170616 MGI Created by mouse qtl pipeline PMID:12297623 1357488 Splq3_m spleen weight QTL 3 (mouse) qtl MP:0004953 decreased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357488 Splq3_m spleen weight QTL 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357488 Splq3_m spleen weight QTL 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357490 Hlbsb2_m hepatic lipase activity in BSB 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15314098 1357490 Hlbsb2_m hepatic lipase activity in BSB 2 (mouse) qtl MP:0011581 increased triglyceride lipase activity IAGP N RGD:5509061 20120209 MGI PMID:15314098 1357491 Fmgty3_m femur geometry 3 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357491 Fmgty3_m femur geometry 3 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357491 Fmgty3_m femur geometry 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357492 Tgct5_m testicular germ cell tumor 5 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12566386 1357492 Tgct5_m testicular germ cell tumor 5 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12566386 1357492 Tgct5_m testicular germ cell tumor 5 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12566386 1357492 Tgct5_m testicular germ cell tumor 5 (mouse) qtl MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:12566386 1357493 Lgaq3_m late growth adjusted QTL 3 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 1357493 Lgaq3_m late growth adjusted QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1357494 Obsty2_m obesity 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357494 Obsty2_m obesity 2 (mouse) qtl MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357495 Gpdc1_m G protein deficiency-induced colitis 1 (mouse) qtl MP:0002816 colitis IAGP N RGD:5509061 20111116 MGI PMID:15633125 1357495 Gpdc1_m G protein deficiency-induced colitis 1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15633125 1357495 Gpdc1_m G protein deficiency-induced colitis 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15633125 1357496 Lptl2_m LPS-induced pulmonary TNF-alpha locus 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15177550 1357496 Lptl2_m LPS-induced pulmonary TNF-alpha locus 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15177550 1357496 Lptl2_m LPS-induced pulmonary TNF-alpha locus 2 (mouse) qtl MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20111116 MGI PMID:15177550 1357497 Stzid2_m streptozotocin induced diabetes susceptibility 2 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:12879252 1357497 Stzid2_m streptozotocin induced diabetes susceptibility 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12879252 1357498 Noan2_m nitrous oxide antinociception 2 (mouse) qtl MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20111116 MGI PMID:14706786 1357498 Noan2_m nitrous oxide antinociception 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14706786 1357498 Noan2_m nitrous oxide antinociception 2 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14706786 1357499 Depmq1_m dependence on morphine QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457340 1357499 Depmq1_m dependence on morphine QTL 1 (mouse) qtl MP:0009753 enhanced behavioral response to morphine IAGP N RGD:5509061 20111116 MGI PMID:15457340 1357500 Mdmsc6_m modifier of muscularity 6 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:14504233 1357500 Mdmsc6_m modifier of muscularity 6 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14504233 1357502 Pnhdlc2_m plasma non-HDL cholesterol 2 (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12810823 1357502 Pnhdlc2_m plasma non-HDL cholesterol 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12810823 1357503 Nhdlq5_m non-HDL QTL 5 (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:15210844 1357503 Nhdlq5_m non-HDL QTL 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15210844 1357504 Mhstq1_m male hybrid sterility QTL 1 (mouse) qtl MP:0001147 small testis IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357504 Mhstq1_m male hybrid sterility QTL 1 (mouse) qtl MP:0001169 abnormal bulbourethral gland morphology IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357504 Mhstq1_m male hybrid sterility QTL 1 (mouse) qtl MP:0001925 male infertility IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357504 Mhstq1_m male hybrid sterility QTL 1 (mouse) qtl MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357504 Mhstq1_m male hybrid sterility QTL 1 (mouse) qtl MP:0002717 abnormal male preputial gland morphology IAGP N RGD:5509061 20121214 MGI PMID:15389318 1357504 Mhstq1_m male hybrid sterility QTL 1 (mouse) qtl MP:0004852 decreased testis weight IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357504 Mhstq1_m male hybrid sterility QTL 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15389318 1357504 Mhstq1_m male hybrid sterility QTL 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15389318 1357504 Mhstq1_m male hybrid sterility QTL 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:15389318 1357504 Mhstq1_m male hybrid sterility QTL 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15389318 1357504 Mhstq1_m male hybrid sterility QTL 1 (mouse) qtl MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357504 Mhstq1_m male hybrid sterility QTL 1 (mouse) qtl MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357504 Mhstq1_m male hybrid sterility QTL 1 (mouse) qtl MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357504 Mhstq1_m male hybrid sterility QTL 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15389318 1357505 Vtbt1_m vertebral trabecular bone trait 1 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357505 Vtbt1_m vertebral trabecular bone trait 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357506 W10q6_m weight 10 weeks QTL 6 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1357506 W10q6_m weight 10 weeks QTL 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1357507 Synch2_m synechia 2 (mouse) qtl MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20111116 MGI PMID:15161859 1357507 Synch2_m synechia 2 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15161859 1357508 Sle14_m systematic lupus erythematosus susceptibility 14 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:15034079 1357508 Sle14_m systematic lupus erythematosus susceptibility 14 (mouse) qtl MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:15034079 1357508 Sle14_m systematic lupus erythematosus susceptibility 14 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:15034079 1357508 Sle14_m systematic lupus erythematosus susceptibility 14 (mouse) qtl MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20111116 MGI PMID:15034079 1357510 Hdl40_m HDL level 40 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:9077551 1357510 Hdl40_m HDL level 40 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9077551 1357511 Kidq3_m kidney weight QTL 3 (mouse) qtl MP:0003918 decreased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357511 Kidq3_m kidney weight QTL 3 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357512 Bsbob5_m BSB obesity 5 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15166164 1357512 Bsbob5_m BSB obesity 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15166164 1357512 Bsbob5_m BSB obesity 5 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:15166164 1357512 Bsbob5_m BSB obesity 5 (mouse) qtl MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:15166164 1357513 Bwnd2wk2_m body weight, NMR1 x DBA, 2 week, QTL 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15457339 1357513 Bwnd2wk2_m body weight, NMR1 x DBA, 2 week, QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 1357514 Mbis3_m Mycobacterium bovis-induced systemic lupus erythematosus 3 (mouse) qtl MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:10903779 1357514 Mbis3_m Mycobacterium bovis-induced systemic lupus erythematosus 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10903779 1357515 Lfq2_m live fetuses QTL 2 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672592 1357515 Lfq2_m live fetuses QTL 2 (mouse) qtl MP:0010769 abnormal survival IAGP N RGD:5509061 20111116 MGI PMID:15672592 1357517 Bwtn1_m body weight at necropsy 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357517 Bwtn1_m body weight at necropsy 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357518 Tgyl1_m triglyceride level 1 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357518 Tgyl1_m triglyceride level 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357519 Vtbt12_m vertebral trabecular bone trait 12 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357519 Vtbt12_m vertebral trabecular bone trait 12 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357521 Bsbob4_m BSB obesity 4 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:15166164 1357521 Bsbob4_m BSB obesity 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15166164 1357521 Bsbob4_m BSB obesity 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15166164 1357521 Bsbob4_m BSB obesity 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15166164 1357521 Bsbob4_m BSB obesity 4 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:15166164 1357522 Cia32_m collagen induced arthritis 32 (mouse) qtl MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20111116 MGI PMID:15611280 1357522 Cia32_m collagen induced arthritis 32 (mouse) qtl MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:15716976 1357522 Cia32_m collagen induced arthritis 32 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15611280 1357522 Cia32_m collagen induced arthritis 32 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15611280 1357523 Cia31_m collagen induced arthritis 31 (mouse) qtl MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20111116 MGI PMID:15611280 1357523 Cia31_m collagen induced arthritis 31 (mouse) qtl MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:15716976 1357523 Cia31_m collagen induced arthritis 31 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15611280 1357523 Cia31_m collagen induced arthritis 31 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15611280 1357524 W6q14_m weight 6 weeks QTL 14 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1357524 W6q14_m weight 6 weeks QTL 14 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1357525 Pnhdlc3_m plasma non-HDL cholesterol 3 (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12810823 1357525 Pnhdlc3_m plasma non-HDL cholesterol 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12810823 1357526 Hyplip2_m hyperlipidemia 2 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:15331434 1357526 Hyplip2_m hyperlipidemia 2 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:15331434 1357526 Hyplip2_m hyperlipidemia 2 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:15331434 1357526 Hyplip2_m hyperlipidemia 2 (mouse) qtl MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20111116 MGI PMID:15331434 1357526 Hyplip2_m hyperlipidemia 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9974430 1357526 Hyplip2_m hyperlipidemia 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9974430 1357527 Epfpq1_m epididymal fat percentage QTL 1 (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357527 Epfpq1_m epididymal fat percentage QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357528 Nhdlq3_m non-HDL QTL 3 (mouse) qtl MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20111116 MGI PMID:14872007 1357528 Nhdlq3_m non-HDL QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14872007 1357529 Lvrq8_m liver weight QTL 8 (mouse) qtl MP:0003402 decreased liver weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357529 Lvrq8_m liver weight QTL 8 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357530 Bwnd2wk5_m body weight, NMR1 x DBA, 2 week, QTL 5 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15457339 1357530 Bwnd2wk5_m body weight, NMR1 x DBA, 2 week, QTL 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 1357532 Bmch7_m bone mechanical trait 7 (mouse) qtl MP:0001542 abnormal bone strength IAGP N RGD:5509061 20111116 MGI PMID:15312250 1357532 Bmch7_m bone mechanical trait 7 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15312250 1357533 Nwa2_m New Zealand White autoimmunity 2 (mouse) qtl MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:8805679 1357533 Nwa2_m New Zealand White autoimmunity 2 (mouse) qtl MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20111116 MGI PMID:8805679 1357533 Nwa2_m New Zealand White autoimmunity 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8805679 1357534 Cinda3_m cytokine induced activation 3 (mouse) qtl MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:15551356 1357534 Cinda3_m cytokine induced activation 3 (mouse) qtl MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:15551356 1357534 Cinda3_m cytokine induced activation 3 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15551356 1357534 Cinda3_m cytokine induced activation 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15551356 1357534 Cinda3_m cytokine induced activation 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15551356 1357535 Arigg2_m anti-RBC IgG antibodies 2 (mouse) qtl MP:0004797 increased anti-erythrocyte antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357535 Arigg2_m anti-RBC IgG antibodies 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357536 Fmgty5_m femur geometry 5 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357536 Fmgty5_m femur geometry 5 (mouse) qtl MP:0001542 abnormal bone strength IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357536 Fmgty5_m femur geometry 5 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357536 Fmgty5_m femur geometry 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357537 Lith12_m lithogenic gene 12 (mouse) qtl MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20111116 MGI PMID:12837957 1357537 Lith12_m lithogenic gene 12 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:16151694 1357537 Lith12_m lithogenic gene 12 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12837957|PMID:16151694 1357537 Lith12_m lithogenic gene 12 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12837957|PMID:16151694 1357538 Espq4_m embryo survival preimplantation QTL 4 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672592 1357538 Espq4_m embryo survival preimplantation QTL 4 (mouse) qtl MP:0010769 abnormal survival IAGP N RGD:5509061 20111116 MGI PMID:15672592 1357539 Bsbob3_m BSB obesity 3 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:15166164 1357539 Bsbob3_m BSB obesity 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15166164 1357540 Mp53d1_m modifier of p53-deficiency 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12592396 1357540 Mp53d1_m modifier of p53-deficiency 1 (mouse) qtl MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20111116 MGI PMID:12592396 1357541 Hdl34_m HDL level 34 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:9077551 1357541 Hdl34_m HDL level 34 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9077551 1357543 Arigm5_m anti-RBC IgM antibodies 5 (mouse) qtl MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357543 Arigm5_m anti-RBC IgM antibodies 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357543 Arigm5_m anti-RBC IgM antibodies 5 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15373903 1357544 Vtbt10_m vertebral trabecular bone trait 10 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357544 Vtbt10_m vertebral trabecular bone trait 10 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357545 Bwnd4wk4_m body weight, NMR1 x DBA, 4 week, QTL 4 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15457339 1357545 Bwnd4wk4_m body weight, NMR1 x DBA, 4 week, QTL 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 1357546 Vtbt3_m vertebral trabecular bone trait 3 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357546 Vtbt3_m vertebral trabecular bone trait 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357550 Alcdp1_m alcohol dependency 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11919667 1357550 Alcdp1_m alcohol dependency 1 (mouse) qtl MP:0009775 increased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:11919667 1357551 Stzid_m streptozotocin induced diabetes susceptibility (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:12879252 1357551 Stzid_m streptozotocin induced diabetes susceptibility (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15670764|PMID:12879252 1357551 Stzid_m streptozotocin induced diabetes susceptibility (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15670764|PMID:12879252 1357551 Stzid_m streptozotocin induced diabetes susceptibility (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:12879252 1357551 Stzid_m streptozotocin induced diabetes susceptibility (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15670764|PMID:12879252 1357552 Aaj4_m anxiety in A/J 4 (mouse) qtl MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:15371360 1357552 Aaj4_m anxiety in A/J 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15371360 1357555 Tesq2_m testis weight QTL 2 (mouse) qtl MP:0004852 decreased testis weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357555 Tesq2_m testis weight QTL 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357555 Tesq2_m testis weight QTL 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357557 Etan1_m ether anesthesia 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15549469 1357557 Etan1_m ether anesthesia 1 (mouse) qtl MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20111116 MGI PMID:15549469 1357558 Bmch4_m bone mechanical trait 4 (mouse) qtl MP:0001542 abnormal bone strength IAGP N RGD:5509061 20111116 MGI PMID:15312250 1357558 Bmch4_m bone mechanical trait 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15312250 1357559 Scfq2_m subcutaneous fat pad weight QTL 2 (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357559 Scfq2_m subcutaneous fat pad weight QTL 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357561 Mbsyd_m metabolic syndrome (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15514201 1357561 Mbsyd_m metabolic syndrome (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:15514201 1357561 Mbsyd_m metabolic syndrome (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15514201 1357561 Mbsyd_m metabolic syndrome (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15514201 1357562 Hmdc_m heterogeneity of muscle Gapd decay constants (mouse) qtl MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20111116 MGI PMID:15519297 1357562 Hmdc_m heterogeneity of muscle Gapd decay constants (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15519297 1357563 Bmch6_m bone mechanical trait 6 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:15312250 1357563 Bmch6_m bone mechanical trait 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15312250 1357565 wrmod1_m wobbler modifier 1 (mouse) qtl MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20111116 MGI PMID:11930176 1357565 wrmod1_m wobbler modifier 1 (mouse) qtl MP:0002183 gliosis IAGP N RGD:5509061 20111116 MGI PMID:11930176 1357565 wrmod1_m wobbler modifier 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11930176 1357566 Lfq3_m live fetuses QTL 3 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672592 1357566 Lfq3_m live fetuses QTL 3 (mouse) qtl MP:0010769 abnormal survival IAGP N RGD:5509061 20111116 MGI PMID:15672592 1357567 Nidd3k_m Nidd3 on KK-A<y> (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:12115031 1357567 Nidd3k_m Nidd3 on KK-A<y> (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115031 1357567 Nidd3k_m Nidd3 on KK-A<y> (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115031 1357567 Nidd3k_m Nidd3 on KK-A<y> (mouse) qtl MP:0006353 increased glycosylated hemoglobin level IAGP N RGD:5509061 20111116 MGI PMID:12115031 1357569 Fmgty13_m femur geometry 13 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357569 Fmgty13_m femur geometry 13 (mouse) qtl MP:0001542 abnormal bone strength IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357569 Fmgty13_m femur geometry 13 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357569 Fmgty13_m femur geometry 13 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357570 Pltct1_m platelet count 1 (mouse) qtl MP:0003179 thrombocytopenia IAGP N RGD:5509061 20111116 MGI PMID:15520881 1357570 Pltct1_m platelet count 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15520881 1357571 Hrtq2_m heart weight QTL 2 (mouse) qtl MP:0002834 decreased heart weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357571 Hrtq2_m heart weight QTL 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357573 Fmgty2_m femur geometry 2 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357573 Fmgty2_m femur geometry 2 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357573 Fmgty2_m femur geometry 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357574 Hcif1_m hepatocarcinogenesis in females 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8650181 1357574 Hcif1_m hepatocarcinogenesis in females 1 (mouse) qtl MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20111116 MGI PMID:8650181 1357574 Hcif1_m hepatocarcinogenesis in females 1 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:8650181 1357574 Hcif1_m hepatocarcinogenesis in females 1 (mouse) qtl MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8650181 1357575 Wt10q2_m body weight, 10 weeks, QTL 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:10353911 1357575 Wt10q2_m body weight, 10 weeks, QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1357577 Trmq3_m T cell ratio modifier QTL 3 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:15529344 1357577 Trmq3_m T cell ratio modifier QTL 3 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:17082620 1357577 Trmq3_m T cell ratio modifier QTL 3 (mouse) qtl MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:15529344 1357577 Trmq3_m T cell ratio modifier QTL 3 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15529344 1357577 Trmq3_m T cell ratio modifier QTL 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15529344 1357577 Trmq3_m T cell ratio modifier QTL 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15529344 1357578 Manln5_m mandible length 5 (mouse) qtl MP:0004593 long mandible IAGP N RGD:5509061 20111116 MGI PMID:15384169 1357578 Manln5_m mandible length 5 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357578 Manln5_m mandible length 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357579 Dmyaq3_m darker modification of yellow agouti QTL 3 (mouse) qtl MP:0001186 pigmentation phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12859623 1357579 Dmyaq3_m darker modification of yellow agouti QTL 3 (mouse) qtl MP:0005409 darkened coat color IAGP N RGD:5509061 20111116 MGI PMID:12859623 1357579 Dmyaq3_m darker modification of yellow agouti QTL 3 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12859623 1357580 Pltct2_m platelet count 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15520881 1357580 Pltct2_m platelet count 2 (mouse) qtl MP:0005505 thrombocytosis IAGP N RGD:5509061 20111116 MGI PMID:15520881 1357581 Manln6_m mandible length 6 (mouse) qtl MP:0004593 long mandible IAGP N RGD:5509061 20111116 MGI PMID:15384169 1357581 Manln6_m mandible length 6 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357581 Manln6_m mandible length 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357582 Splq9_m spleen weight QTL 9 (mouse) qtl MP:0004953 decreased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357582 Splq9_m spleen weight QTL 9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357582 Splq9_m spleen weight QTL 9 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357583 Sle18_m systematic lupus erythematosus susceptibility 18 (mouse) qtl MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20111116 MGI PMID:15314659 1357583 Sle18_m systematic lupus erythematosus susceptibility 18 (mouse) qtl MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:16943797 1357583 Sle18_m systematic lupus erythematosus susceptibility 18 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:16943797 1357583 Sle18_m systematic lupus erythematosus susceptibility 18 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16943797|PMID:15314659 1357583 Sle18_m systematic lupus erythematosus susceptibility 18 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:15314659 1357584 Splq6_m spleen weight QTL 6 (mouse) qtl MP:0004953 decreased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357584 Splq6_m spleen weight QTL 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357584 Splq6_m spleen weight QTL 6 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357585 Manln3_m mandible length 3 (mouse) qtl MP:0004593 long mandible IAGP N RGD:5509061 20111116 MGI PMID:15384169 1357585 Manln3_m mandible length 3 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357585 Manln3_m mandible length 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357586 Mdmsc3_m modifier of muscularity 3 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:14504233 1357586 Mdmsc3_m modifier of muscularity 3 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14504233 1357588 Manln18_m mandible length 18 (mouse) qtl MP:0004593 long mandible IAGP N RGD:5509061 20111116 MGI PMID:15384169 1357588 Manln18_m mandible length 18 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357588 Manln18_m mandible length 18 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357589 Kdnw2_m kidney weight 2 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357589 Kdnw2_m kidney weight 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357589 Kdnw2_m kidney weight 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15561968 1357590 Bwnd2wk7_m body weight, NMR1 x DBA, 2 week, QTL 7 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15457339 1357590 Bwnd2wk7_m body weight, NMR1 x DBA, 2 week, QTL 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 1357591 Tesq1_m testis weight QTL 1 (mouse) qtl MP:0004852 decreased testis weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357591 Tesq1_m testis weight QTL 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357591 Tesq1_m testis weight QTL 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357594 Estoq3_m embryo survival total QTL 3 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672592 1357594 Estoq3_m embryo survival total QTL 3 (mouse) qtl MP:0010769 abnormal survival IAGP N RGD:5509061 20111116 MGI PMID:15672592 1357595 Phrtq1_m percent heart QTL 1 (mouse) qtl MP:0002834 decreased heart weight IAGP N RGD:5509061 20111116 MGI PMID:10353911 1357595 Phrtq1_m percent heart QTL 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1357596 Tgct3_m testicular germ cell tumor 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12566386 1357596 Tgct3_m testicular germ cell tumor 3 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12566386 1357596 Tgct3_m testicular germ cell tumor 3 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12566386 1357596 Tgct3_m testicular germ cell tumor 3 (mouse) qtl MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:12566386 1357597 Arigm7_m anti-RBC IgM antibodies 7 (mouse) qtl MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357597 Arigm7_m anti-RBC IgM antibodies 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357597 Arigm7_m anti-RBC IgM antibodies 7 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15373903 1357599 msrvh1_m modifier of susceptibility to renal vascular hypertrophy/hyperplasia 1 (mouse) qtl MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20111116 MGI PMID:14718357 1357599 msrvh1_m modifier of susceptibility to renal vascular hypertrophy/hyperplasia 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14718357 1357599 msrvh1_m modifier of susceptibility to renal vascular hypertrophy/hyperplasia 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14718357 1357600 Obq17_m obesity QTL 17 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15210844 1357600 Obq17_m obesity QTL 17 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15210844 1357600 Obq17_m obesity QTL 17 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:15210844 1357600 Obq17_m obesity QTL 17 (mouse) qtl MP:0006087 increased body mass index IAGP N RGD:5509061 20111116 MGI PMID:15210844 1357601 Manln9_m mandible length 9 (mouse) qtl MP:0004593 long mandible IAGP N RGD:5509061 20111116 MGI PMID:15384169 1357601 Manln9_m mandible length 9 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357601 Manln9_m mandible length 9 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357602 Vtbt2_m vertebral trabecular bone trait 2 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357602 Vtbt2_m vertebral trabecular bone trait 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357605 Mdmsc5_m modifier of muscularity 5 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:14504233 1357605 Mdmsc5_m modifier of muscularity 5 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14504233 1357606 Lgdr1_m liver Gapd decay rate 1 (mouse) qtl MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20111116 MGI PMID:15519297 1357606 Lgdr1_m liver Gapd decay rate 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15519297 1357610 Vtbt8_m vertebral trabecular bone trait 8 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357610 Vtbt8_m vertebral trabecular bone trait 8 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357612 Epfpq2_m epididymal fat percentage QTL 2 (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357612 Epfpq2_m epididymal fat percentage QTL 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357613 Bsbob2_m BSB obesity 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15166164 1357613 Bsbob2_m BSB obesity 2 (mouse) qtl MP:0001781 abnormal white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:15166164 1357613 Bsbob2_m BSB obesity 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15166164 1357613 Bsbob2_m BSB obesity 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15166164 1357613 Bsbob2_m BSB obesity 2 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:15166164 1357614 Bmca_m bile mucin accumulation (mouse) qtl MP:0004773 abnormal bile composition IAGP N RGD:5509061 20111116 MGI PMID:12395324 1357614 Bmca_m bile mucin accumulation (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12395324 1357617 Mp53d3_m modifier of p53-deficiency 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12592396 1357617 Mp53d3_m modifier of p53-deficiency 3 (mouse) qtl MP:0004503 decreased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20111116 MGI PMID:12592396 1357617 Mp53d3_m modifier of p53-deficiency 3 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:12592396 1357617 Mp53d3_m modifier of p53-deficiency 3 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12592396 1357618 Splq5_m spleen weight QTL 5 (mouse) qtl MP:0004953 decreased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357618 Splq5_m spleen weight QTL 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357618 Splq5_m spleen weight QTL 5 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357619 Obsty5_m obesity 5 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357619 Obsty5_m obesity 5 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357619 Obsty5_m obesity 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357619 Obsty5_m obesity 5 (mouse) qtl MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357619 Obsty5_m obesity 5 (mouse) qtl MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357619 Obsty5_m obesity 5 (mouse) qtl MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357620 Aaj1_m anxiety in A/J 1 (mouse) qtl MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:15371360 1357620 Aaj1_m anxiety in A/J 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15371360 1357621 Bmch3_m bone mechanical trait 3 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:15312250 1357621 Bmch3_m bone mechanical trait 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15312250 1357622 Espq3_m embryo survival preimplantation QTL 3 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672592 1357622 Espq3_m embryo survival preimplantation QTL 3 (mouse) qtl MP:0010769 abnormal survival IAGP N RGD:5509061 20111116 MGI PMID:15672592 1357623 Fmgty10_m femur geometry 10 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357623 Fmgty10_m femur geometry 10 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357623 Fmgty10_m femur geometry 10 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357624 Arigm6_m anti-RBC IgM antibodies 6 (mouse) qtl MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357624 Arigm6_m anti-RBC IgM antibodies 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357624 Arigm6_m anti-RBC IgM antibodies 6 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15373903 1357626 Arigg9_m anti-RBC IgG antibodies 9 (mouse) qtl MP:0004797 increased anti-erythrocyte antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357626 Arigg9_m anti-RBC IgG antibodies 9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357627 Tgq2_m triglyceride QTL 2 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:15210844 1357627 Tgq2_m triglyceride QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15210844 1357628 Manln13_m mandible length 13 (mouse) qtl MP:0004593 long mandible IAGP N RGD:5509061 20111116 MGI PMID:15384169 1357628 Manln13_m mandible length 13 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357628 Manln13_m mandible length 13 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357630 Tgq1_m triglyceride QTL 1 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:15210844 1357630 Tgq1_m triglyceride QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15210844 1357631 Motr1_m modifier of tubby retinal degeneration 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12076089 1357631 Motr1_m modifier of tubby retinal degeneration 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12076089 1357631 Motr1_m modifier of tubby retinal degeneration 1 (mouse) qtl MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20111116 MGI PMID:12076089 1357631 Motr1_m modifier of tubby retinal degeneration 1 (mouse) qtl MP:0006070 increased retina photoreceptor cell number IAGP N RGD:5509061 20111116 MGI PMID:12076089 1357632 Vtbt9_m vertebral trabecular bone trait 9 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357632 Vtbt9_m vertebral trabecular bone trait 9 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357634 Splq7_m spleen weight QTL 7 (mouse) qtl MP:0004953 decreased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357634 Splq7_m spleen weight QTL 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357634 Splq7_m spleen weight QTL 7 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357635 Splq4_m spleen weight QTL 4 (mouse) qtl MP:0004953 decreased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357635 Splq4_m spleen weight QTL 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357635 Splq4_m spleen weight QTL 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357636 Arigm4_m anti-RBC IgM antibodies 4 (mouse) qtl MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357636 Arigm4_m anti-RBC IgM antibodies 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357636 Arigm4_m anti-RBC IgM antibodies 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15373903 1357639 Obsty4_m obesity 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357639 Obsty4_m obesity 4 (mouse) qtl MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357640 Orq2_m ovulation rate QTL 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672592 1357640 Orq2_m ovulation rate QTL 2 (mouse) qtl MP:0031411 increased ovulation rate IAGP N RGD:5509061 20220804 MGI PMID:15672592 1357641 Arigm1_m anti-RBC IgM antibodies 1 (mouse) qtl MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357641 Arigm1_m anti-RBC IgM antibodies 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357641 Arigm1_m anti-RBC IgM antibodies 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15373903 1357642 Dmyaq1_m darker modification of yellow agouti QTL 1 (mouse) qtl MP:0001186 pigmentation phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12859623 1357642 Dmyaq1_m darker modification of yellow agouti QTL 1 (mouse) qtl MP:0005409 darkened coat color IAGP N RGD:5509061 20111116 MGI PMID:12859623 1357642 Dmyaq1_m darker modification of yellow agouti QTL 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12859623 1357645 Lvrq9_m liver weight QTL 9 (mouse) qtl MP:0003402 decreased liver weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357645 Lvrq9_m liver weight QTL 9 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357647 Fmgty7_m femur geometry 7 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357647 Fmgty7_m femur geometry 7 (mouse) qtl MP:0001542 abnormal bone strength IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357647 Fmgty7_m femur geometry 7 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357647 Fmgty7_m femur geometry 7 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357648 Obq18_m obesity QTL 18 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15210844 1357648 Obq18_m obesity QTL 18 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15210844 1357648 Obq18_m obesity QTL 18 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:15210844 1357649 Cbm5_m cerebellum weight 5 (mouse) qtl MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20111116 MGI PMID:11438585 1357649 Cbm5_m cerebellum weight 5 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11438585 1357651 Lgq5_m late growth QTL 5 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 1357651 Lgq5_m late growth QTL 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1357652 Xydsq_m X/Y dissociation QTL (mouse) qtl MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357652 Xydsq_m X/Y dissociation QTL (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20240510 MGI Created by mouse qtl pipeline PMID:15389318 1357652 Xydsq_m X/Y dissociation QTL (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15389318 1357653 Rthyd2_m resistance to thymic deletion 2 (mouse) qtl MP:0005002 abnormal T cell clonal deletion IAGP N RGD:5509061 20111116 MGI PMID:15589170 1357653 Rthyd2_m resistance to thymic deletion 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15589170 1357653 Rthyd2_m resistance to thymic deletion 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15589170 1357653 Rthyd2_m resistance to thymic deletion 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15589170 1357654 Manln14_m mandible length 14 (mouse) qtl MP:0004593 long mandible IAGP N RGD:5509061 20111116 MGI PMID:15384169 1357654 Manln14_m mandible length 14 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357654 Manln14_m mandible length 14 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357655 Capsq2_m capsaicin sensitivity related QTL 2 (mouse) qtl MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20111116 MGI PMID:14499433 1357655 Capsq2_m capsaicin sensitivity related QTL 2 (mouse) qtl MP:0005394 taste/olfaction phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14499433 1357656 Hrtq3_m heart weight QTL 3 (mouse) qtl MP:0002834 decreased heart weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357656 Hrtq3_m heart weight QTL 3 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357657 Pymr_m Plasmodium yoelli malaria resistance (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:11862405 1357657 Pymr_m Plasmodium yoelli malaria resistance (mouse) qtl MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:11862405 1357657 Pymr_m Plasmodium yoelli malaria resistance (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11862405 1357659 Epfpq4_m epididymal fat percentage QTL 4 (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:14657254 1357659 Epfpq4_m epididymal fat percentage QTL 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357661 Eae2b_m susceptibility to experimental allergic encephalomyelitis 2b (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517969 1357661 Eae2b_m susceptibility to experimental allergic encephalomyelitis 2b (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517969 1357661 Eae2b_m susceptibility to experimental allergic encephalomyelitis 2b (mouse) qtl MP:0006082 CNS inflammation IAGP N RGD:5509061 20111116 MGI PMID:12517969 1357662 Lprq4_m lipoprotein QTL 4 (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:7560076 1357662 Lprq4_m lipoprotein QTL 4 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:7560076 1357662 Lprq4_m lipoprotein QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18048852|PMID:7560076 1357662 Lprq4_m lipoprotein QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150612 MGI Created by mouse qtl pipeline PMID:7560076 1357663 Rthyd1_m resistance to thymic deletion 1 (mouse) qtl MP:0005002 abnormal T cell clonal deletion IAGP N RGD:5509061 20111116 MGI PMID:15589170 1357663 Rthyd1_m resistance to thymic deletion 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15589170 1357663 Rthyd1_m resistance to thymic deletion 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15589170 1357663 Rthyd1_m resistance to thymic deletion 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15589170 1357664 Nba3_m New Zealand Black autoimmunity 3 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12215897 1357664 Nba3_m New Zealand Black autoimmunity 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12215897 1357665 Hlq1_m heat loss QTL 1 (mouse) qtl MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20111116 MGI PMID:10353911 1357665 Hlq1_m heat loss QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 1357667 Heal12_m wound healing/regeneration 12 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:15225218 1357667 Heal12_m wound healing/regeneration 12 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15225218 1357668 Espq1_m embryo survival preimplantation QTL 1 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672592 1357668 Espq1_m embryo survival preimplantation QTL 1 (mouse) qtl MP:0010769 abnormal survival IAGP N RGD:5509061 20111116 MGI PMID:15672592 1357669 Lprq1_m lipoprotein QTL 1 (mouse) qtl MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:9974430 1357669 Lprq1_m lipoprotein QTL 1 (mouse) qtl MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:9974430 1357669 Lprq1_m lipoprotein QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9974430 1357672 Marif1_m macrophage-associated risk inflammatory factor 1 (mouse) qtl MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20111116 MGI PMID:15150098 1357672 Marif1_m macrophage-associated risk inflammatory factor 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15150098 1357672 Marif1_m macrophage-associated risk inflammatory factor 1 (mouse) qtl MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20111116 MGI PMID:15150098 1357672 Marif1_m macrophage-associated risk inflammatory factor 1 (mouse) qtl MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20111116 MGI PMID:15150098 1357673 Arigg7_m anti-RBC IgG antibodies 7 (mouse) qtl MP:0004797 increased anti-erythrocyte antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357673 Arigg7_m anti-RBC IgG antibodies 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357674 Eae27_m experimental allergic encephalomyelitis susceptibility 27 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517969 1357674 Eae27_m experimental allergic encephalomyelitis susceptibility 27 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517969 1357674 Eae27_m experimental allergic encephalomyelitis susceptibility 27 (mouse) qtl MP:0006082 CNS inflammation IAGP N RGD:5509061 20111116 MGI PMID:12517969 1357675 Manln17_m mandible length 17 (mouse) qtl MP:0004593 long mandible IAGP N RGD:5509061 20111116 MGI PMID:15384169 1357675 Manln17_m mandible length 17 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357675 Manln17_m mandible length 17 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357676 Tilss1_m TNF-induced lethal shock susceptibility 1 (mouse) qtl MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20111116 MGI PMID:17404289 1357676 Tilss1_m TNF-induced lethal shock susceptibility 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12089334|PMID:17404289 1357679 Egrm1_m early growth rate, maternal effect 1 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20150409 MGI PMID:12242647 1357679 Egrm1_m early growth rate, maternal effect 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12242647 1357680 Idd23_m insulin dependent diabetes susceptibility 23 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:15561967 1357680 Idd23_m insulin dependent diabetes susceptibility 23 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561967 1357681 Hrtq1_m heart weight QTL 1 (mouse) qtl MP:0002834 decreased heart weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357681 Hrtq1_m heart weight QTL 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357682 Phdlc1_m plasma HDL cholesterol 1 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12810823 1357682 Phdlc1_m plasma HDL cholesterol 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12810823 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:11033447 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:11918215 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:15549416 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20111116 MGI PMID:11918215 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:11918215 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20111116 MGI PMID:15549416 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0002139 abnormal hepatobiliary system physiology IAGP N RGD:5509061 20111116 MGI PMID:15549416 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0003109 short femur IAGP N RGD:5509061 20111116 MGI PMID:11918215 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20160609 MGI PMID:11033447 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20160609 MGI PMID:15542029 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20201002 MGI PMID:11918215 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20201002 MGI PMID:15549416 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11033447 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11033447 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11033447 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11033447 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:11033447 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11033447 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:15549416 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:11918215 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:15542029 1357683 Igf1sl1_m IGF-1 serum levels 1 (mouse) qtl MP:0021190 decreased bone mineral density of lumbar vertebrae IAGP N RGD:5509061 20220915 MGI PMID:15542029 1357684 Bmch5_m bone mechanical trait 5 (mouse) qtl MP:0001542 abnormal bone strength IAGP N RGD:5509061 20111116 MGI PMID:15312250 1357684 Bmch5_m bone mechanical trait 5 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:15312250 1357684 Bmch5_m bone mechanical trait 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15312250 1357685 Skts13_m skin tumor sucseptibility 13 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12881723 1357685 Skts13_m skin tumor sucseptibility 13 (mouse) qtl MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20111116 MGI PMID:12881723 1357685 Skts13_m skin tumor sucseptibility 13 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12881723 1357686 Lmblgq2_m limb length QTL 2 (mouse) qtl MP:0004350 long humerus IAGP N RGD:5509061 20111116 MGI PMID:12118102 1357686 Lmblgq2_m limb length QTL 2 (mouse) qtl MP:0004370 long ulna IAGP N RGD:5509061 20111116 MGI PMID:12118102 1357686 Lmblgq2_m limb length QTL 2 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1357686 Lmblgq2_m limb length QTL 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1357688 Mgdr1_m muscle Gapd decay rate 1 (mouse) qtl MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20111116 MGI PMID:15519297 1357688 Mgdr1_m muscle Gapd decay rate 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15519297 1357689 Mdmsc1_m modifier of muscularity 1 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:14504233 1357689 Mdmsc1_m modifier of muscularity 1 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14504233 1357690 Vtbt19_m vertebral trabecular bone trait 19 (mouse) qtl MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357690 Vtbt19_m vertebral trabecular bone trait 19 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357693 Tcsz1_m tooth central size 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:11973311 1357693 Tcsz1_m tooth central size 1 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11973311 1357693 Tcsz1_m tooth central size 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20171006 MGI Created by mouse qtl pipeline PMID:11973311 1357693 Tcsz1_m tooth central size 1 (mouse) qtl MP:0030091 macrodontia IAGP N RGD:5509061 20171005 MGI PMID:11973311 1357694 Fmgty1_m femur geometry 1 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357694 Fmgty1_m femur geometry 1 (mouse) qtl MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357694 Fmgty1_m femur geometry 1 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357694 Fmgty1_m femur geometry 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357695 Pbrgcsf2_m peripheral blood stem cell response to granulocyte colony stimulating factor 2 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:14725902 1357695 Pbrgcsf2_m peripheral blood stem cell response to granulocyte colony stimulating factor 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10688851 1357696 Cia30_m collagen induced arthritis 30 (mouse) qtl MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20111116 MGI PMID:15611280 1357696 Cia30_m collagen induced arthritis 30 (mouse) qtl MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:15611280 1357696 Cia30_m collagen induced arthritis 30 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15611280 1357696 Cia30_m collagen induced arthritis 30 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15611280 1357697 Carfhg2_m carcass fat in high growth mice 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11309659 1357697 Carfhg2_m carcass fat in high growth mice 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:11309659 1357697 Carfhg2_m carcass fat in high growth mice 2 (mouse) qtl MP:0010024 increased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:11309659 1357697 Carfhg2_m carcass fat in high growth mice 2 (mouse) qtl MP:0010024 increased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:16670015 1357698 Arigg6_m anti-RBC IgG antibodies 6 (mouse) qtl MP:0004797 increased anti-erythrocyte antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357698 Arigg6_m anti-RBC IgG antibodies 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357699 Nhdlq6_m non-HDL QTL 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15210844 1357700 Thyct1_m thymocyte count 1 (mouse) qtl MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20111116 MGI PMID:12944977 1357700 Thyct1_m thymocyte count 1 (mouse) qtl MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20111116 MGI PMID:12944977 1357700 Thyct1_m thymocyte count 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:12944977 1357700 Thyct1_m thymocyte count 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12944977 1357700 Thyct1_m thymocyte count 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12944977 1357701 Lvrq10_m liver weight QTL 10 (mouse) qtl MP:0003402 decreased liver weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357701 Lvrq10_m liver weight QTL 10 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357702 Anth2_m resistance to Bacillus anthracis 2 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:3143893 1357702 Anth2_m resistance to Bacillus anthracis 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:3143893 1357703 Vtbt17_m vertebral trabecular bone trait 17 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357703 Vtbt17_m vertebral trabecular bone trait 17 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357706 Lvrq2_m liver weight QTL 2 (mouse) qtl MP:0003402 decreased liver weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357706 Lvrq2_m liver weight QTL 2 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357707 Elpfm_m eye lens protein fluorescence emission (mouse) qtl MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20111116 MGI PMID:15519297 1357707 Elpfm_m eye lens protein fluorescence emission (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15519297 1357708 Orq1_m ovulation rate QTL 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672592 1357708 Orq1_m ovulation rate QTL 1 (mouse) qtl MP:0031411 increased ovulation rate IAGP N RGD:5509061 20220804 MGI PMID:15672592 1357710 Arigm3_m anti-RBC IgM antibodies 3 (mouse) qtl MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357710 Arigm3_m anti-RBC IgM antibodies 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357710 Arigm3_m anti-RBC IgM antibodies 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15373903 1357711 Adbg1_m adult body growth 1 (mouse) qtl MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357711 Adbg1_m adult body growth 1 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357711 Adbg1_m adult body growth 1 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357711 Adbg1_m adult body growth 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357713 Afpq9_m abdominal fat percent QTL 9 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:11116089 1357713 Afpq9_m abdominal fat percent QTL 9 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089 1357716 Bwnd5wk3_m body weight, NMR1 x DBA, 5 week, QTL 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15457339 1357716 Bwnd5wk3_m body weight, NMR1 x DBA, 5 week, QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 1357717 Hlpx_m heterogeneity in eye lens protein photooxidation kinetics (mouse) qtl MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20111116 MGI PMID:15519297 1357717 Hlpx_m heterogeneity in eye lens protein photooxidation kinetics (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15519297 1357719 Hipp3_m hippocampal weight 3 (mouse) qtl MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20111116 MGI PMID:12953790 1357719 Hipp3_m hippocampal weight 3 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12953790 1357720 Kidpq1_m kidney weight percentage QTL 1 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357720 Kidpq1_m kidney weight percentage QTL 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357720 Kidpq1_m kidney weight percentage QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15058381 1357721 Sle17_m systematic lupus erythematosus susceptibility 17 (mouse) qtl MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20111116 MGI PMID:15314659 1357721 Sle17_m systematic lupus erythematosus susceptibility 17 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15314659 1357722 Vtbt11_m vertebral trabecular bone trait 11 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357722 Vtbt11_m vertebral trabecular bone trait 11 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357724 Fmgty6_m femur geometry 6 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357724 Fmgty6_m femur geometry 6 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357724 Fmgty6_m femur geometry 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357725 Eae39_m experimental allergic encephalomyelitis 39 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517969 1357725 Eae39_m experimental allergic encephalomyelitis 39 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12517969 1357725 Eae39_m experimental allergic encephalomyelitis 39 (mouse) qtl MP:0006082 CNS inflammation IAGP N RGD:5509061 20111116 MGI PMID:12517969 1357726 Lnopy1_m lens opacity 1 (mouse) qtl MP:0001304 cataract IAGP N RGD:5509061 20111116 MGI PMID:15161859 1357726 Lnopy1_m lens opacity 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15161859 1357728 ecl1_m epistatic circling C57L/J 1 (mouse) qtl MP:0001394 circling IAGP N RGD:5509061 20111116 MGI PMID:11932245 1357729 Marif2_m macrophage-associated risk inflammatory factor 2 (mouse) qtl MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20111116 MGI PMID:15150098 1357729 Marif2_m macrophage-associated risk inflammatory factor 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15150098 1357729 Marif2_m macrophage-associated risk inflammatory factor 2 (mouse) qtl MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20111116 MGI PMID:15150098 1357729 Marif2_m macrophage-associated risk inflammatory factor 2 (mouse) qtl MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20111116 MGI PMID:15150098 1357730 Hstx1_m hybrid sterility, X chromosome 1 (mouse) qtl MP:0001925 male infertility IAGP N RGD:5509061 20111116 MGI PMID:15366371 1357730 Hstx1_m hybrid sterility, X chromosome 1 (mouse) qtl MP:0002687 oligozoospermia IAGP N RGD:5509061 20111116 MGI PMID:15366371 1357730 Hstx1_m hybrid sterility, X chromosome 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15366371 1357730 Hstx1_m hybrid sterility, X chromosome 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15366371 1357730 Hstx1_m hybrid sterility, X chromosome 1 (mouse) qtl MP:0005578 teratozoospermia IAGP N RGD:5509061 20111116 MGI PMID:15366371 1357731 Lvrq6_m liver weight QTL 6 (mouse) qtl MP:0003402 decreased liver weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357731 Lvrq6_m liver weight QTL 6 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357734 Nba5_m New Zealand Black autoimmunity 5 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:15634937 1357734 Nba5_m New Zealand Black autoimmunity 5 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15634937 1357734 Nba5_m New Zealand Black autoimmunity 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15634937 1357734 Nba5_m New Zealand Black autoimmunity 5 (mouse) qtl MP:0005615 increased susceptibility to type III hypersensitivity reaction IAGP N RGD:5509061 20111116 MGI PMID:15634937 1357735 Arigg3_m anti-RBC IgG antibodies 3 (mouse) qtl MP:0004797 increased anti-erythrocyte antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357735 Arigg3_m anti-RBC IgG antibodies 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357737 Hpcr2_m hepatocarcinogen resistance 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7705639 1357737 Hpcr2_m hepatocarcinogen resistance 2 (mouse) qtl MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20111116 MGI PMID:7705639 1357737 Hpcr2_m hepatocarcinogen resistance 2 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:7705639 1357737 Hpcr2_m hepatocarcinogen resistance 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7705639 1357737 Hpcr2_m hepatocarcinogen resistance 2 (mouse) qtl MP:0010265 decreased hepatoma incidence IAGP N RGD:5509061 20111116 MGI PMID:7705639 1357738 Estoq2_m embryo survival total QTL 2 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672592 1357738 Estoq2_m embryo survival total QTL 2 (mouse) qtl MP:0010769 abnormal survival IAGP N RGD:5509061 20111116 MGI PMID:15672592 1357739 Vtbt16_m vertebral trabecular bone trait 16 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357739 Vtbt16_m vertebral trabecular bone trait 16 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357740 Obsty3_m obesity 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357740 Obsty3_m obesity 3 (mouse) qtl MP:0002833 increased heart weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357740 Obsty3_m obesity 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357740 Obsty3_m obesity 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357740 Obsty3_m obesity 3 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357740 Obsty3_m obesity 3 (mouse) qtl MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357740 Obsty3_m obesity 3 (mouse) qtl MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357740 Obsty3_m obesity 3 (mouse) qtl MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357740 Obsty3_m obesity 3 (mouse) qtl MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357741 Nidd5k_m Nidd5 on KK-A<y> (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:12115031 1357741 Nidd5k_m Nidd5 on KK-A<y> (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115031 1357743 Lith3_m lithogenic gene 3 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:12395324 1357743 Lith3_m lithogenic gene 3 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12395324 1357744 Cfbw4_m cystic fibrosis body weight 4 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:12461646 1357744 Cfbw4_m cystic fibrosis body weight 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12461646 1357745 Scfq4_m subcutaneous fat pad weight QTL 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357745 Scfq4_m subcutaneous fat pad weight QTL 4 (mouse) qtl MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357745 Scfq4_m subcutaneous fat pad weight QTL 4 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357746 Vtbt7_m vertebral trabecular bone trait 7 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357746 Vtbt7_m vertebral trabecular bone trait 7 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357747 Fob3a_m F-line obesity QTL 3a (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:15181539 1357747 Fob3a_m F-line obesity QTL 3a (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15181539 1357747 Fob3a_m F-line obesity QTL 3a (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15181539 1357747 Fob3a_m F-line obesity QTL 3a (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:15181539 1357749 Vtbt13_m vertebral trabecular bone trait 13 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357749 Vtbt13_m vertebral trabecular bone trait 13 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357750 Gpdc2_m G protein deficiency-induced colitis 2 (mouse) qtl MP:0002816 colitis IAGP N RGD:5509061 20111116 MGI PMID:15633125 1357750 Gpdc2_m G protein deficiency-induced colitis 2 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15633125 1357750 Gpdc2_m G protein deficiency-induced colitis 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15633125 1357751 ecl2_m epistatic circling C57L/J 2 (mouse) qtl MP:0001394 circling IAGP N RGD:5509061 20111116 MGI PMID:11932245 1357752 Tabw_m tally ho asscoiated body weight (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:11414755 1357752 Tabw_m tally ho asscoiated body weight (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11414755 1357753 Kidq2_m kidney weight QTL 2 (mouse) qtl MP:0003918 decreased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357753 Kidq2_m kidney weight QTL 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357754 Ahl3_m age related hearing loss 3 (mouse) qtl MP:0004766 decreased susceptibility to age-related hearing loss IAGP N RGD:5509061 20111116 MGI PMID:15504353 1357754 Ahl3_m age related hearing loss 3 (mouse) qtl MP:0005377 hearing/vestibular/ear phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15504353 1357757 Lnopy2_m lens opacity 2 (mouse) qtl MP:0001304 cataract IAGP N RGD:5509061 20111116 MGI PMID:15161859 1357757 Lnopy2_m lens opacity 2 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15161859 1357758 Lptl1_m LPS-induced pulmonary TNF-alpha locus 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15177550 1357758 Lptl1_m LPS-induced pulmonary TNF-alpha locus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15177550 1357758 Lptl1_m LPS-induced pulmonary TNF-alpha locus 1 (mouse) qtl MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20111116 MGI PMID:15177550 1357759 W3q12_m weight 3 weeks QTL 12 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1357759 W3q12_m weight 3 weeks QTL 12 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1357760 Synch3_m synechia 3 (mouse) qtl MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20111116 MGI PMID:15161859 1357760 Synch3_m synechia 3 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15161859 1357761 Lfq1_m live fetuses QTL 1 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672592 1357761 Lfq1_m live fetuses QTL 1 (mouse) qtl MP:0010769 abnormal survival IAGP N RGD:5509061 20111116 MGI PMID:15672592 1357762 Splq2_m spleen weight QTL 2 (mouse) qtl MP:0004953 decreased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357762 Splq2_m spleen weight QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357762 Splq2_m spleen weight QTL 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357764 Athla1_m atherosclerotic lesion area 1 (mouse) qtl MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20111116 MGI PMID:15514201 1357764 Athla1_m atherosclerotic lesion area 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15514201 1357765 Cmcs_m cerebral malaria susceptibility in CBA/N (mouse) qtl MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20111116 MGI PMID:15536567 1357765 Cmcs_m cerebral malaria susceptibility in CBA/N (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15536567 1357767 Arigg5_m anti-RBC IgG antibodies 5 (mouse) qtl MP:0004797 increased anti-erythrocyte antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357767 Arigg5_m anti-RBC IgG antibodies 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357768 Baa1_m BALB/c autoimmunity 1 (mouse) qtl MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:8805679 1357768 Baa1_m BALB/c autoimmunity 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8805679 1357768 Baa1_m BALB/c autoimmunity 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:8805679 1357772 Scfq1_m subcutaneous fat pad weight QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357772 Scfq1_m subcutaneous fat pad weight QTL 1 (mouse) qtl MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357772 Scfq1_m subcutaneous fat pad weight QTL 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357773 Espq2_m embryo survival preimplantation QTL 2 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672592 1357773 Espq2_m embryo survival preimplantation QTL 2 (mouse) qtl MP:0010769 abnormal survival IAGP N RGD:5509061 20111116 MGI PMID:15672592 1357774 Fmgty8_m femur geometry 8 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357774 Fmgty8_m femur geometry 8 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357774 Fmgty8_m femur geometry 8 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357775 Pbwg9_m postnatal body weight growth 9 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15056934 1357775 Pbwg9_m postnatal body weight growth 9 (mouse) qtl MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20111116 MGI PMID:16174331 1357779 Tesq3_m testis weight QTL 3 (mouse) qtl MP:0004851 increased testis weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357779 Tesq3_m testis weight QTL 3 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357779 Tesq3_m testis weight QTL 3 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357784 Arti2_m age related thymic involution 2 (mouse) qtl MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20111116 MGI PMID:12944977 1357784 Arti2_m age related thymic involution 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:12944977 1357784 Arti2_m age related thymic involution 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12944977 1357784 Arti2_m age related thymic involution 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12944977 1357785 Cinda2_m cytokine induced activation 2 (mouse) qtl MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:9177770 1357785 Cinda2_m cytokine induced activation 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9177770 1357785 Cinda2_m cytokine induced activation 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9177770 1357785 Cinda2_m cytokine induced activation 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9177770 1357787 Vtbt5_m vertebral trabecular bone trait 5 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357787 Vtbt5_m vertebral trabecular bone trait 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357788 ecl_m epistatic circling C57L/J (mouse) qtl MP:0001394 circling IAGP N RGD:5509061 20111116 MGI PMID:11932245 1357789 Kdnw3_m kidney weight 3 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15561968 1357789 Kdnw3_m kidney weight 3 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561968 1357789 Kdnw3_m kidney weight 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15561968 1357793 Pnhdlc1_m plasma non-HDL cholesterol 1 (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12810823 1357793 Pnhdlc1_m plasma non-HDL cholesterol 1 (mouse) qtl MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18048852 1357793 Pnhdlc1_m plasma non-HDL cholesterol 1 (mouse) qtl MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18048852 1357793 Pnhdlc1_m plasma non-HDL cholesterol 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18048852|PMID:12810823 1357793 Pnhdlc1_m plasma non-HDL cholesterol 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:12810823 1357794 Cinda1_m cytokine induced activation 1 (mouse) qtl MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:9177770 1357794 Cinda1_m cytokine induced activation 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9177770 1357794 Cinda1_m cytokine induced activation 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9177770 1357794 Cinda1_m cytokine induced activation 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9177770 1357795 Hdlcl2_m HDL cholesterol level 2 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:15514201 1357795 Hdlcl2_m HDL cholesterol level 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15514201 1357796 Trmq5_m T cell ratio modifier QTL 5 (mouse) qtl MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:15611280 1357796 Trmq5_m T cell ratio modifier QTL 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15611280 1357796 Trmq5_m T cell ratio modifier QTL 5 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15611280 1357797 Splq8_m spleen weight QTL 8 (mouse) qtl MP:0004953 decreased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357797 Splq8_m spleen weight QTL 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357797 Splq8_m spleen weight QTL 8 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357799 Igf1sl3_m IGF-1 serum levels 3 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20201001 MGI PMID:11033447 1357799 Igf1sl3_m IGF-1 serum levels 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11033447 1357800 Tgq3_m triglyceride QTL 3 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:15210844 1357800 Tgq3_m triglyceride QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15210844 1357801 Kidq7_m kidney weight QTL 7 (mouse) qtl MP:0003918 decreased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357801 Kidq7_m kidney weight QTL 7 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357802 Vtbt15_m vertebral trabecular bone trait 15 (mouse) qtl MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:15005846 1357802 Vtbt15_m vertebral trabecular bone trait 15 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15005846 1357804 Mhstq2_m male hybrid sterility QTL 2 (mouse) qtl MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357804 Mhstq2_m male hybrid sterility QTL 2 (mouse) qtl MP:0001925 male infertility IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357804 Mhstq2_m male hybrid sterility QTL 2 (mouse) qtl MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357804 Mhstq2_m male hybrid sterility QTL 2 (mouse) qtl MP:0003179 thrombocytopenia IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357804 Mhstq2_m male hybrid sterility QTL 2 (mouse) qtl MP:0004852 decreased testis weight IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357804 Mhstq2_m male hybrid sterility QTL 2 (mouse) qtl MP:0005159 azoospermia IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357804 Mhstq2_m male hybrid sterility QTL 2 (mouse) qtl MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357804 Mhstq2_m male hybrid sterility QTL 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15389318 1357804 Mhstq2_m male hybrid sterility QTL 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15389318 1357804 Mhstq2_m male hybrid sterility QTL 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15389318 1357804 Mhstq2_m male hybrid sterility QTL 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15389318 1357804 Mhstq2_m male hybrid sterility QTL 2 (mouse) qtl MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357804 Mhstq2_m male hybrid sterility QTL 2 (mouse) qtl MP:0009234 absent sperm head IAGP N RGD:5509061 20111116 MGI PMID:15389318 1357806 Aaj3_m anxiety in A/J 3 (mouse) qtl MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:15371360 1357806 Aaj3_m anxiety in A/J 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15371360 1357807 Arigg1_m anti-RBC IgG antibodies 1 (mouse) qtl MP:0004797 increased anti-erythrocyte antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357807 Arigg1_m anti-RBC IgG antibodies 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357808 Mgdr2_m muscle Gapd decay rate 2 (mouse) qtl MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20111116 MGI PMID:15519297 1357808 Mgdr2_m muscle Gapd decay rate 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15519297 1357811 Orq3_m ovulation rate QTL 3 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672592 1357811 Orq3_m ovulation rate QTL 3 (mouse) qtl MP:0031411 increased ovulation rate IAGP N RGD:5509061 20220804 MGI PMID:15672592 1357812 Kidq6_m kidney weight QTL 6 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357812 Kidq6_m kidney weight QTL 6 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357812 Kidq6_m kidney weight QTL 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15058381 1357813 Ath20_m atherosclerosis 20 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:14592847 1357813 Ath20_m atherosclerosis 20 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592847 1357814 Hcs5_m hepatocarcinogenesis susceptibility 5 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7829059 1357814 Hcs5_m hepatocarcinogenesis susceptibility 5 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:7829059 1357814 Hcs5_m hepatocarcinogenesis susceptibility 5 (mouse) qtl MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20111116 MGI PMID:7829059 1357815 Fmgty4_m femur geometry 4 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357815 Fmgty4_m femur geometry 4 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357815 Fmgty4_m femur geometry 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357816 Fmgty14_m femur geometry 14 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357816 Fmgty14_m femur geometry 14 (mouse) qtl MP:0001542 abnormal bone strength IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357816 Fmgty14_m femur geometry 14 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357816 Fmgty14_m femur geometry 14 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357817 Dmyaq2_m darker modification of yellow agouti QTL 2 (mouse) qtl MP:0001186 pigmentation phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12859623 1357817 Dmyaq2_m darker modification of yellow agouti QTL 2 (mouse) qtl MP:0005409 darkened coat color IAGP N RGD:5509061 20111116 MGI PMID:12859623 1357817 Dmyaq2_m darker modification of yellow agouti QTL 2 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12859623 1357818 Grwtj1_m growth trajectory 1 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15304622 1357818 Grwtj1_m growth trajectory 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15304622 1357819 Tgct2_m testicular germ cell tumor 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12566386 1357819 Tgct2_m testicular germ cell tumor 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12566386 1357819 Tgct2_m testicular germ cell tumor 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12566386 1357819 Tgct2_m testicular germ cell tumor 2 (mouse) qtl MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:12566386 1357821 Arigg8_m anti-RBC IgG antibodies 8 (mouse) qtl MP:0004797 increased anti-erythrocyte antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357821 Arigg8_m anti-RBC IgG antibodies 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357822 Lvrq3_m liver weight QTL 3 (mouse) qtl MP:0003402 decreased liver weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357822 Lvrq3_m liver weight QTL 3 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357823 Spha3_m sperm head anomaly 3 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15020476 1357823 Spha3_m sperm head anomaly 3 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15020476 1357823 Spha3_m sperm head anomaly 3 (mouse) qtl MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20111116 MGI PMID:15020476 1357824 Estoq4_m embryo survival total QTL 4 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672592 1357824 Estoq4_m embryo survival total QTL 4 (mouse) qtl MP:0010769 abnormal survival IAGP N RGD:5509061 20111116 MGI PMID:15672592 1357825 Kidpq2_m kidney weight percentage QTL 2 (mouse) qtl MP:0003918 decreased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357825 Kidpq2_m kidney weight percentage QTL 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357826 Arti1_m age related thymic involution 1 (mouse) qtl MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20111116 MGI PMID:12944977 1357826 Arti1_m age related thymic involution 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:12944977 1357826 Arti1_m age related thymic involution 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12944977 1357826 Arti1_m age related thymic involution 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12944977 1357827 Hdl39_m HDL level 39 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:9077551 1357827 Hdl39_m HDL level 39 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9077551 1357828 Fmgty12_m femur geometry 12 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357828 Fmgty12_m femur geometry 12 (mouse) qtl MP:0001542 abnormal bone strength IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357828 Fmgty12_m femur geometry 12 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357828 Fmgty12_m femur geometry 12 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357829 Lvrq1_m liver weight QTL 1 (mouse) qtl MP:0003402 decreased liver weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357829 Lvrq1_m liver weight QTL 1 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357831 Igf1sl2_m IGF-1 serum levels 2 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:16675518 1357831 Igf1sl2_m IGF-1 serum levels 2 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20201001 MGI PMID:11033447 1357831 Igf1sl2_m IGF-1 serum levels 2 (mouse) qtl MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20111116 MGI PMID:16675518 1357831 Igf1sl2_m IGF-1 serum levels 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11033447 1357831 Igf1sl2_m IGF-1 serum levels 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11033447 1357831 Igf1sl2_m IGF-1 serum levels 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11033447 1357831 Igf1sl2_m IGF-1 serum levels 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11033447 1357831 Igf1sl2_m IGF-1 serum levels 2 (mouse) qtl MP:0005568 increased circulating total protein level IAGP N RGD:5509061 20111116 MGI PMID:11033447 1357831 Igf1sl2_m IGF-1 serum levels 2 (mouse) qtl MP:0005568 increased circulating total protein level IAGP N RGD:5509061 20111116 MGI PMID:16675518 1357835 Mp53d2_m modifier of p53-deficiency 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12592396 1357835 Mp53d2_m modifier of p53-deficiency 2 (mouse) qtl MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20111116 MGI PMID:12592396 1357837 Alcdp2_m alcohol dependency 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11919667 1357837 Alcdp2_m alcohol dependency 2 (mouse) qtl MP:0009775 increased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:11919667 1357838 Noan1_m nitrous oxide antinociception 1 (mouse) qtl MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20111116 MGI PMID:14706786 1357838 Noan1_m nitrous oxide antinociception 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14706786 1357838 Noan1_m nitrous oxide antinociception 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14706786 1357840 Lppl1_m LPS-induced pulmonary PMN locus 1 (mouse) qtl MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20111116 MGI PMID:15177550 1357840 Lppl1_m LPS-induced pulmonary PMN locus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15177550 1357840 Lppl1_m LPS-induced pulmonary PMN locus 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15177550 1357841 Phdlc2_m plasma HDL cholesterol 2 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12810823 1357841 Phdlc2_m plasma HDL cholesterol 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12810823 1357842 Hipp5_m hippocampal weight 5 (mouse) qtl MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20111116 MGI PMID:12953790 1357842 Hipp5_m hippocampal weight 5 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12953790 1357845 Rthyd3_m resistance to thymic deletion 3 (mouse) qtl MP:0005002 abnormal T cell clonal deletion IAGP N RGD:5509061 20111116 MGI PMID:15589170 1357845 Rthyd3_m resistance to thymic deletion 3 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15589170 1357845 Rthyd3_m resistance to thymic deletion 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15589170 1357845 Rthyd3_m resistance to thymic deletion 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15589170 1357849 Lbm8_m lean body mass 8 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:12185457 1357849 Lbm8_m lean body mass 8 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12185457 1357851 Scfq3_m subcutaneous fat pad weight QTL 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357851 Scfq3_m subcutaneous fat pad weight QTL 3 (mouse) qtl MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357851 Scfq3_m subcutaneous fat pad weight QTL 3 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357852 Manln8_m mandible length 8 (mouse) qtl MP:0004593 long mandible IAGP N RGD:5509061 20111116 MGI PMID:15384169 1357852 Manln8_m mandible length 8 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357852 Manln8_m mandible length 8 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357853 Dfq1_m dead fetuses QTL 1 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672592 1357853 Dfq1_m dead fetuses QTL 1 (mouse) qtl MP:0010769 abnormal survival IAGP N RGD:5509061 20111116 MGI PMID:15672592 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0001859 kidney inflammation IAGP N RGD:5509061 20120727 MGI PMID:21724994 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20120727 MGI PMID:21724994 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20120727 MGI PMID:21724994 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20111116 MGI PMID:15314659 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0002871 albuminuria IAGP N RGD:5509061 20120727 MGI PMID:21724994 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20120727 MGI PMID:21724994 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:17277141 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:16943797 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:16943797 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:16943797 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:16943797 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:17277141 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20111116 MGI PMID:16943797 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20120727 MGI PMID:21724994 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120720 MGI Created by mouse qtl pipeline PMID:16943797|PMID:15314659 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:15314659 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120720 MGI Created by mouse qtl pipeline PMID:16943797|PMID:15314659 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:15314659 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120720 MGI Created by mouse qtl pipeline PMID:16943797|PMID:15314659 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:15314659 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16943797|PMID:15314659 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:15314659 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120720 MGI Created by mouse qtl pipeline PMID:16943797|PMID:15314659 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:15314659 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120720 MGI Created by mouse qtl pipeline PMID:16943797|PMID:15314659 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:15314659 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120720 MGI Created by mouse qtl pipeline PMID:16943797|PMID:15314659 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20160205 MGI Created by mouse qtl pipeline PMID:15314659 1357854 Sle16_m systematic lupus erythematosus susceptibility 16 (mouse) qtl MP:0011508 abnormal glomerular capillary thrombosis IAGP N RGD:5509061 20120727 MGI PMID:21724994 1357855 Fob3b_m F-line obesity QTL 3b (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20151119 MGI PMID:15181539 1357855 Fob3b_m F-line obesity QTL 3b (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15181539 1357855 Fob3b_m F-line obesity QTL 3b (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15181539 1357855 Fob3b_m F-line obesity QTL 3b (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20151119 MGI PMID:15181539 1357856 Baa2_m BALB/c autoimmunity 2 (mouse) qtl MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:8805679 1357856 Baa2_m BALB/c autoimmunity 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8805679 1357856 Baa2_m BALB/c autoimmunity 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:8805679 1357857 Lvrq5_m liver weight QTL 5 (mouse) qtl MP:0003402 decreased liver weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357857 Lvrq5_m liver weight QTL 5 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357859 Lvrq7_m liver weight QTL 7 (mouse) qtl MP:0003402 decreased liver weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357859 Lvrq7_m liver weight QTL 7 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357860 Aorls1_m aortic lesion size 1 (mouse) qtl MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20111116 MGI PMID:12925895 1357860 Aorls1_m aortic lesion size 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12925895 1357861 Bwnd4wk7_m body weight, NMR1 x DBA, 4 week, QTL 7 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15457339 1357861 Bwnd4wk7_m body weight, NMR1 x DBA, 4 week, QTL 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 1357862 Epfq1_m epididymal fat pad weight QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357862 Epfq1_m epididymal fat pad weight QTL 1 (mouse) qtl MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357862 Epfq1_m epididymal fat pad weight QTL 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357863 Thyct2_m thymocyte count 2 (mouse) qtl MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20111116 MGI PMID:12944977 1357863 Thyct2_m thymocyte count 2 (mouse) qtl MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20111116 MGI PMID:12944977 1357863 Thyct2_m thymocyte count 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:12944977 1357863 Thyct2_m thymocyte count 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12944977 1357863 Thyct2_m thymocyte count 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12944977 1357864 Scfpq1_m subcutaneous fat pad percentage QTL 1 (mouse) qtl MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357864 Scfpq1_m subcutaneous fat pad percentage QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357866 Bwnd3wk1_m body weight, NMR1 x DBA, 3 week, QTL 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15457339 1357866 Bwnd3wk1_m body weight, NMR1 x DBA, 3 week, QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 1357868 Manln11_m mandible length 11 (mouse) qtl MP:0004593 long mandible IAGP N RGD:5509061 20111116 MGI PMID:15384169 1357868 Manln11_m mandible length 11 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357868 Manln11_m mandible length 11 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357869 Fmgty11_m femur geometry 11 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357869 Fmgty11_m femur geometry 11 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357869 Fmgty11_m femur geometry 11 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357871 Bmch1_m bone mechanical trait 1 (mouse) qtl MP:0001542 abnormal bone strength IAGP N RGD:5509061 20111116 MGI PMID:15312250 1357871 Bmch1_m bone mechanical trait 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15312250 1357872 Arigm2_m anti-RBC IgM antibodies 2 (mouse) qtl MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:15373903 1357872 Arigm2_m anti-RBC IgM antibodies 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15373903 1357872 Arigm2_m anti-RBC IgM antibodies 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15373903 1357874 Manln1_m mandible length 1 (mouse) qtl MP:0004593 long mandible IAGP N RGD:5509061 20111116 MGI PMID:15384169 1357874 Manln1_m mandible length 1 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357874 Manln1_m mandible length 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1357876 Bdmsq_m body mass QTL (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15339634 1357876 Bdmsq_m body mass QTL (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15339634 1357877 Synch1_m synechia 1 (mouse) qtl MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20111116 MGI PMID:15161859 1357877 Synch1_m synechia 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15161859 1357878 Mastr_m modifier of astrocytoma (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15319471 1357878 Mastr_m modifier of astrocytoma (mouse) qtl MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:15319471 1357878 Mastr_m modifier of astrocytoma (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15319471 1357878 Mastr_m modifier of astrocytoma (mouse) qtl MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20111116 MGI PMID:15319471 1357879 Swrl1_m SWR lupus locus 1 (mouse) qtl MP:0002532 abnormal type II hypersensitivity reaction IAGP N RGD:5509061 20111116 MGI PMID:11739537 1357879 Swrl1_m SWR lupus locus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12215897 1357879 Swrl1_m SWR lupus locus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20170505 MGI Created by mouse qtl pipeline PMID:11739537|PMID:12215897 1357879 Swrl1_m SWR lupus locus 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:12215897 1357879 Swrl1_m SWR lupus locus 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20170505 MGI Created by mouse qtl pipeline PMID:11739537|PMID:12215897 1357879 Swrl1_m SWR lupus locus 1 (mouse) qtl MP:0008502 increased IgG3 level IAGP N RGD:5509061 20111116 MGI PMID:12215897 1357881 Estoq1_m embryo survival total QTL 1 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672592 1357881 Estoq1_m embryo survival total QTL 1 (mouse) qtl MP:0010769 abnormal survival IAGP N RGD:5509061 20111116 MGI PMID:15672592 1357882 Rthyd5_m resistance to thymic deletion 5 (mouse) qtl MP:0005002 abnormal T cell clonal deletion IAGP N RGD:5509061 20111116 MGI PMID:15589170 1357882 Rthyd5_m resistance to thymic deletion 5 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15589170 1357882 Rthyd5_m resistance to thymic deletion 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15589170 1357882 Rthyd5_m resistance to thymic deletion 5 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15589170 1357883 Epfq5_m epididymal fat pad weight QTL 5 (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357883 Epfq5_m epididymal fat pad weight QTL 5 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357885 Bwnd5wk7_m body weight, NMR1 x DBA, 5 week, QTL 7 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15457339 1357885 Bwnd5wk7_m body weight, NMR1 x DBA, 5 week, QTL 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 1357886 Diht_m dopamine-induced hypothermia (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15672594 1357886 Diht_m dopamine-induced hypothermia (mouse) qtl MP:0005534 decreased body temperature IAGP N RGD:5509061 20111116 MGI PMID:15672594 1357887 Cinda4_m cytokine induced activation 4 (mouse) qtl MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:15551356 1357887 Cinda4_m cytokine induced activation 4 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15551356 1357887 Cinda4_m cytokine induced activation 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15551356 1357887 Cinda4_m cytokine induced activation 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15551356 1357888 Aibl_m adiposity index and body length (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20111116 MGI PMID:15181538 1357888 Aibl_m adiposity index and body length (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15181538 1357889 Lprq3_m lipoprotein QTL 3 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:7560076 1357889 Lprq3_m lipoprotein QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7560076 1357889 Lprq3_m lipoprotein QTL 3 (mouse) qtl MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20111116 MGI PMID:7560076 1357890 Hpcr1_m hepatocarcinogen resistance 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7705639 1357890 Hpcr1_m hepatocarcinogen resistance 1 (mouse) qtl MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20111116 MGI PMID:7705639 1357890 Hpcr1_m hepatocarcinogen resistance 1 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:7705639 1357890 Hpcr1_m hepatocarcinogen resistance 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7705639 1357890 Hpcr1_m hepatocarcinogen resistance 1 (mouse) qtl MP:0010265 decreased hepatoma incidence IAGP N RGD:5509061 20111116 MGI PMID:7705639 1357891 Hcif2_m hepatocarcinogenesis in females 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8650181 1357891 Hcif2_m hepatocarcinogenesis in females 2 (mouse) qtl MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20111116 MGI PMID:8650181 1357891 Hcif2_m hepatocarcinogenesis in females 2 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:8650181 1357891 Hcif2_m hepatocarcinogenesis in females 2 (mouse) qtl MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8650181 1357892 Marif3_m macrophage-associated risk inflammatory factor 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15150098 1357892 Marif3_m macrophage-associated risk inflammatory factor 3 (mouse) qtl MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20111116 MGI PMID:15150098 1357893 Lvrq4_m liver weight QTL 4 (mouse) qtl MP:0003402 decreased liver weight IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357893 Lvrq4_m liver weight QTL 4 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357894 Epfpq3_m epididymal fat percentage QTL 3 (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:15058381 1357894 Epfpq3_m epididymal fat percentage QTL 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058381 1357895 Ctrcts_m cataract severity (mouse) qtl MP:0001304 cataract IAGP N RGD:5509061 20111116 MGI PMID:15161859 1357895 Ctrcts_m cataract severity (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15161859 1357897 Lprq2_m lipoprotein QTL 2 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:9974430 1357897 Lprq2_m lipoprotein QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9974430 1357898 Fmgty9_m femur geometry 9 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357898 Fmgty9_m femur geometry 9 (mouse) qtl MP:0001542 abnormal bone strength IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357898 Fmgty9_m femur geometry 9 (mouse) qtl MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20111116 MGI PMID:12929939 1357898 Fmgty9_m femur geometry 9 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357898 Fmgty9_m femur geometry 9 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12929939 1357901 Mdmsc2_m modifier of muscularity 2 (mouse) qtl MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20111116 MGI PMID:14504233 1357901 Mdmsc2_m modifier of muscularity 2 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14504233 1357902 Obq19_m obesity QTL 19 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15210844 1357902 Obq19_m obesity QTL 19 (mouse) qtl MP:0006087 increased body mass index IAGP N RGD:5509061 20111116 MGI PMID:15210844 1357903 Gpdc3_m G protein deficiency-induced colitis 3 (mouse) qtl MP:0002816 colitis IAGP N RGD:5509061 20111116 MGI PMID:15633125 1357903 Gpdc3_m G protein deficiency-induced colitis 3 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15633125 1357903 Gpdc3_m G protein deficiency-induced colitis 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15633125 1357904 Hdl36_m HDL level 36 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:9077551 1357904 Hdl36_m HDL level 36 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9077551 13792742 Ccdc107 coiled-coil domain containing 107 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 13800899 Aap_m active avoidance performance (mouse) qtl MP:0002798 abnormal active avoidance behavior IAGP N RGD:5509061 20181025 MGI PMID:1144596 13800899 Aap_m active avoidance performance (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20181019 MGI Created by mouse qtl pipeline PMID:1144596 14700760 A830031A19Rik RIKEN cDNA A830031A19 gene gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20201231 MGI 15037099 Tel15q telomeric sequence, Chr 15, q arm gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20191128 MGI PMID:23307865 15037503 mt-Rnr2 16S rRNA, mitochondrial gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20191128 MGI PMID:11106380 15037503 mt-Rnr2 16S rRNA, mitochondrial gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20191128 MGI PMID:11106380 15037503 mt-Rnr2 16S rRNA, mitochondrial gene MP:0000751 myopathy IAGP N RGD:5509061 20191128 MGI PMID:11106380 15037503 mt-Rnr2 16S rRNA, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191128 MGI PMID:11106380 15037503 mt-Rnr2 16S rRNA, mitochondrial gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20191128 MGI PMID:11106380 15037503 mt-Rnr2 16S rRNA, mitochondrial gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20191128 MGI PMID:11106380 15037503 mt-Rnr2 16S rRNA, mitochondrial gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20191128 MGI PMID:11106380 15037503 mt-Rnr2 16S rRNA, mitochondrial gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20191128 MGI PMID:11106380 15037503 mt-Rnr2 16S rRNA, mitochondrial gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20191128 MGI PMID:11106380 15037503 mt-Rnr2 16S rRNA, mitochondrial gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20191128 MGI PMID:11106380 15037503 mt-Rnr2 16S rRNA, mitochondrial gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20191128 MGI PMID:11106380 15037503 mt-Rnr2 16S rRNA, mitochondrial gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20191128 MGI PMID:11106380 15037503 mt-Rnr2 16S rRNA, mitochondrial gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20191128 MGI PMID:11106380 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20240404 MGI PMID:35998911 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0001260 increased body weight IAGP N RGD:5509061 20240404 MGI PMID:35998911 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20240404 MGI PMID:35998911 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20240404 MGI PMID:35998911 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20240404 MGI PMID:35998911 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20240404 MGI PMID:35998911 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20240404 MGI PMID:35998911 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20240404 MGI PMID:35998911 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20240404 MGI PMID:35998911 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0005331 insulin resistance IAGP N RGD:5509061 20240404 MGI PMID:35998911 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20240404 MGI PMID:35998911 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20240404 MGI PMID:35998911 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20240404 MGI PMID:35998911 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20240404 MGI PMID:35998911 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20240404 MGI PMID:35998911 15037562 mt-Tl1 tRNA leucine 1, mitochondrial gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20240404 MGI PMID:35998911 15038098 mt-Tk tRNA lysine, mitochondrial gene MP:0000747 muscle weakness IAGP N RGD:5509061 20191128 MGI PMID:24510903 15038098 mt-Tk tRNA lysine, mitochondrial gene MP:0001258 decreased body length IAGP N RGD:5509061 20191128 MGI PMID:24510903 15038098 mt-Tk tRNA lysine, mitochondrial gene MP:0004805 absent oocytes IAGP N RGD:5509061 20191128 MGI PMID:24510903 15038098 mt-Tk tRNA lysine, mitochondrial gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20191128 MGI PMID:24510903 15038209 mt-Tr tRNA arginine, mitochondrial gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20191128 MGI PMID:11175788 15038209 mt-Tr tRNA arginine, mitochondrial gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20191128 MGI PMID:11175788 15038209 mt-Tr tRNA arginine, mitochondrial gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20191128 MGI PMID:21803452 15038577 Tsil thymus specific insertion locus gene MP:0002083 premature death IAGP N RGD:5509061 20191128 MGI PMID:8786139 15038577 Tsil thymus specific insertion locus gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20191128 MGI PMID:8786139 15038577 Tsil thymus specific insertion locus gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20191128 MGI PMID:8786139 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0000161 scoliosis IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20191128 MGI PMID:7628698 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20191128 MGI PMID:7628698 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0002083 premature death IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20191128 MGI PMID:7628698 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0004600 abnormal vertebral transverse process morphology IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0004606 absent vertebral spinous process IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20191128 MGI PMID:7628698 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0006253 clinodactyly IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20191128 MGI PMID:7628698 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0008829 triphalangia IAGP N RGD:5509061 20191128 MGI PMID:7628698 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0008985 hemimelia IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20191128 MGI PMID:7628698 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0010772 abnormal pollex morphology IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0010772 abnormal pollex morphology IAGP N RGD:5509061 20191128 MGI PMID:7628698 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0012528 abnormal zone of polarizing activity morphology IAGP N RGD:5509061 20191128 MGI PMID:7628698 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0030112 zygomatic bone hypoplasia IAGP N RGD:5509061 20191128 MGI PMID:23449628 15038936 Is(In8B2-8B3.1;6C1)1Tshir Insertion, Chr8 B2-B3.1 into Chr 6C1, Toshihiko Shiroishi 1 gene MP:0030835 abnormal ankle joint morphology IAGP N RGD:5509061 20191128 MGI PMID:7628698 15039113 mt-Ta tRNA alanine, mitochondrial gene MP:0002833 increased heart weight IAGP N RGD:5509061 20191128 MGI PMID:27626666 15039113 mt-Ta tRNA alanine, mitochondrial gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20191128 MGI PMID:27626666 15039113 mt-Ta tRNA alanine, mitochondrial gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20191128 MGI PMID:27626666 15039113 mt-Ta tRNA alanine, mitochondrial gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20191128 MGI PMID:27626666 15039113 mt-Ta tRNA alanine, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20191128 MGI PMID:27626666 15039113 mt-Ta tRNA alanine, mitochondrial gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20191128 MGI PMID:27626666 15039113 mt-Ta tRNA alanine, mitochondrial gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20191128 MGI PMID:27626666 15039113 mt-Ta tRNA alanine, mitochondrial gene MP:0013272 abnormal translation IAGP N RGD:5509061 20191128 MGI PMID:27626666 15039113 mt-Ta tRNA alanine, mitochondrial gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20191128 MGI PMID:27626666 1549969 Ush1g USH1 protein network component sans gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:1442008 1549969 Ush1g USH1 protein network component sans gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:16235133 1549969 Ush1g USH1 protein network component sans gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:1927362 1549969 Ush1g USH1 protein network component sans gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0001395 bidirectional circling IEA N RGD:5509061 20111116 MGI 1549969 Ush1g USH1 protein network component sans gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:1442008 1549969 Ush1g USH1 protein network component sans gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:1927362 1549969 Ush1g USH1 protein network component sans gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:1442008 1549969 Ush1g USH1 protein network component sans gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:16235133 1549969 Ush1g USH1 protein network component sans gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:16235133 1549969 Ush1g USH1 protein network component sans gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:1442008 1549969 Ush1g USH1 protein network component sans gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:1927362 1549969 Ush1g USH1 protein network component sans gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:1442008 1549969 Ush1g USH1 protein network component sans gene MP:0003879 abnormal hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:1927362 1549969 Ush1g USH1 protein network component sans gene MP:0004331 vestibular saccular macula degeneration IAGP N RGD:5509061 20141003 MGI PMID:1927362 1549969 Ush1g USH1 protein network component sans gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:1927362 1549969 Ush1g USH1 protein network component sans gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18339676 1549969 Ush1g USH1 protein network component sans gene MP:0004405 absent cochlear hair cells IEA N RGD:5509061 20111116 MGI 1549969 Ush1g USH1 protein network component sans gene MP:0004413 absent cochlear microphonics IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0004466 short cochlear outer hair cells IAGP N RGD:5509061 20141003 MGI PMID:18339676 1549969 Ush1g USH1 protein network component sans gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:1442008 1549969 Ush1g USH1 protein network component sans gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:18339676 1549969 Ush1g USH1 protein network component sans gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:1442008 1549969 Ush1g USH1 protein network component sans gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 1549969 Ush1g USH1 protein network component sans gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0004531 short outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 1549969 Ush1g USH1 protein network component sans gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0004536 short inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0004577 abnormal cochlear hair cell inter-stereocilial links morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 1549969 Ush1g USH1 protein network component sans gene MP:0004578 abnormal cochlear hair bundle tip links morphology IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 1549969 Ush1g USH1 protein network component sans gene MP:0004814 reduced linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 1549969 Ush1g USH1 protein network component sans gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:1927362 1549969 Ush1g USH1 protein network component sans gene MP:0006335 abnormal hearing electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:1442008 1549969 Ush1g USH1 protein network component sans gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:1927362 1549969 Ush1g USH1 protein network component sans gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21436032 1549969 Ush1g USH1 protein network component sans gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:22381527 1549969 Ush1g USH1 protein network component sans gene MP:0030961 abnormal outer hair cell kinocilium location or orientation IAGP N RGD:5509061 20190725 MGI PMID:21436032 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:19497859 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:16950128 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:16950128 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0001967 deafness IAGP N RGD:5509061 20200310 MGI PMID:19497859 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19497859 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:16950128 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:16950128 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20200310 MGI PMID:16950128 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20200310 MGI PMID:20976199 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20200310 MGI PMID:19497859 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20200310 MGI PMID:20976199 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20200310 MGI PMID:19497859 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20200310 MGI PMID:16950128 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20200310 MGI PMID:16950128 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19497859 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:19497859 1549970 Actg1 actin, gamma, cytoplasmic 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:20976199 1549973 Nfatc2ip nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 1549973 Nfatc2ip nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:20133688 1549973 Nfatc2ip nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20211021 MGI 1549973 Nfatc2ip nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1549973 Nfatc2ip nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:20133688 1549973 Nfatc2ip nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:20133688 1549973 Nfatc2ip nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein gene MP:0008091 decreased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:20133688 1549973 Nfatc2ip nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20133688 1549973 Nfatc2ip nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20133688 1549973 Nfatc2ip nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:20133688 1549973 Nfatc2ip nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:20133688 1549973 Nfatc2ip nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:20133688 1549973 Nfatc2ip nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein gene MP:0008697 decreased interleukin-3 secretion IAGP N RGD:5509061 20141003 MGI PMID:20133688 1549973 Nfatc2ip nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20133688 1549973 Nfatc2ip nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:20133688 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18048346 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:18178777 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18048346 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18048346 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18048346 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18178777 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18048346 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002424 abnormal reticulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18454133 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18048346 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18454133 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:18454133 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:18048346 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:18454133 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:18048346 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:18048346 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18048346 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18454133 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18178777 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18178777 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18178777 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18454133 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18178777 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:18178777 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:18178777 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18454133 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:18048346 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:18454133 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18178777 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18178777 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0011177 abnormal erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:17420462 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20160304 MGI PMID:18048346 1549974 Bnip3l BCL2/adenovirus E1B interacting protein 3-like gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:18454133 1549975 Capzb capping actin protein of muscle Z-line subunit beta gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20171221 MGI PMID:28899994 1549975 Capzb capping actin protein of muscle Z-line subunit beta gene MP:0002730 head shaking IAGP N RGD:5509061 20171221 MGI PMID:28899994 1549975 Capzb capping actin protein of muscle Z-line subunit beta gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20171221 MGI PMID:28899994 1549975 Capzb capping actin protein of muscle Z-line subunit beta gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20171221 MGI PMID:28899994 1549975 Capzb capping actin protein of muscle Z-line subunit beta gene MP:0004520 short vestibular hair cell stereocilia IAGP N RGD:5509061 20171221 MGI PMID:28899994 1549975 Capzb capping actin protein of muscle Z-line subunit beta gene MP:0004523 decreased cochlear hair cell stereocilia number IAGP N RGD:5509061 20171221 MGI PMID:28899994 1549975 Capzb capping actin protein of muscle Z-line subunit beta gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20171221 MGI PMID:28899994 1549975 Capzb capping actin protein of muscle Z-line subunit beta gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20171221 MGI PMID:28899994 1549975 Capzb capping actin protein of muscle Z-line subunit beta gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20171221 MGI PMID:28899994 1549975 Capzb capping actin protein of muscle Z-line subunit beta gene MP:0010015 abnormal cuticular plate morphology IAGP N RGD:5509061 20171221 MGI PMID:28899994 1549975 Capzb capping actin protein of muscle Z-line subunit beta gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20171221 MGI PMID:28899994 1549977 Fbxo28 F-box protein 28 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20230601 MGI 1549977 Fbxo28 F-box protein 28 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1549977 Fbxo28 F-box protein 28 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20230601 MGI 1549977 Fbxo28 F-box protein 28 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1549977 Fbxo28 F-box protein 28 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1549978 Hmgn3 high mobility group nucleosomal binding domain 3 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141030 MGI PMID:23620591 1549978 Hmgn3 high mobility group nucleosomal binding domain 3 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141030 MGI PMID:23620591 1549978 Hmgn3 high mobility group nucleosomal binding domain 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19651901 1549978 Hmgn3 high mobility group nucleosomal binding domain 3 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141030 MGI PMID:23620591 1549978 Hmgn3 high mobility group nucleosomal binding domain 3 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141030 MGI PMID:23620591 1549978 Hmgn3 high mobility group nucleosomal binding domain 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19651901 1549978 Hmgn3 high mobility group nucleosomal binding domain 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19651901 1549978 Hmgn3 high mobility group nucleosomal binding domain 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141030 MGI PMID:23620591 1549978 Hmgn3 high mobility group nucleosomal binding domain 3 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141030 MGI PMID:23620591 1549978 Hmgn3 high mobility group nucleosomal binding domain 3 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141030 MGI PMID:23620591 1549978 Hmgn3 high mobility group nucleosomal binding domain 3 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141030 MGI PMID:23620591 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0000111 cleft palate IAGP N RGD:5509061 20200310 MGI PMID:28530676 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20210826 MGI 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20200310 MGI PMID:28530676 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:28530676 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0001293 anophthalmia IEA N RGD:5509061 20210826 MGI 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20200310 MGI PMID:28530676 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20220519 MGI 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0001785 edema IEA N RGD:5509061 20210826 MGI 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0001914 hemorrhage IEA N RGD:5509061 20210826 MGI 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200310 MGI PMID:28530676 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220811 MGI 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20200310 MGI PMID:28530676 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:28530676 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20200310 MGI PMID:28530676 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210826 MGI 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20200310 MGI PMID:28530676 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20200310 MGI PMID:28530676 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28530676 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20200310 MGI PMID:28530676 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0011495 abnormal head shape IEA N RGD:5509061 20210826 MGI 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0013294 prenatal lethality prior to heart atrial septation IAGP N RGD:5509061 20200310 MGI PMID:28530676 1549981 Dzip1l DAZ interacting protein 1-like gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:28530676 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20200310 MGI PMID:27297240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20200310 MGI PMID:22130515 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20200310 MGI PMID:21930766 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000288 abnormal pericardium morphology IAGP N RGD:5509061 20200310 MGI PMID:22926762 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20200310 MGI PMID:24667635 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:16510575 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20200310 MGI PMID:20881014 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20200310 MGI PMID:19738070 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:10953035 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20200310 MGI PMID:22666441 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000754 paresis IAGP N RGD:5509061 20200310 MGI PMID:27297240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200310 MGI PMID:27297240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000906 abnormal trigeminal V mesencephalic nucleus morphology IAGP N RGD:5509061 20221215 MGI PMID:25975378 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:15218525 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:22412863 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000959 abnormal somatic sensory system morphology IAGP N RGD:5509061 20200310 MGI PMID:16906226 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:16906226 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20200310 MGI PMID:20187849 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:16906226 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20221215 MGI PMID:25975378 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20221215 MGI PMID:25975378 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:25100603 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:20364121 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200310 MGI PMID:24430185 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20200310 MGI PMID:25100603 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:22096518 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:12812988 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:25100603 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:27297240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20200310 MGI PMID:25100603 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001426 polydipsia IAGP N RGD:5509061 20200310 MGI PMID:20364121 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20200310 MGI PMID:1528024 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20200310 MGI PMID:24430185 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20200310 MGI PMID:1528024 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:27297240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20200310 MGI PMID:22096518 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20200310 MGI PMID:25100603 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20200310 MGI PMID:3221240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20200310 MGI PMID:20364121 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20221215 MGI PMID:25975378 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001596 hypotension IAGP N RGD:5509061 20200310 MGI PMID:15306694 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20200310 MGI PMID:15798202 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:15218525 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:22723298 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:16461894 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:22723298 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:17491588 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:19064922 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20200310 MGI PMID:20364121 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20200310 MGI PMID:23520048 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20200310 MGI PMID:18821589 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20200310 MGI PMID:16510575 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20200310 MGI PMID:18037992 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19738070 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20200310 MGI PMID:24430185 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:15218525 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:22723298 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20221215 MGI PMID:25975378 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20200310 MGI PMID:12812988 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19064922 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19064922 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19064922 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002047 increased hepatic hemangioma incidence IAGP N RGD:5509061 20200310 MGI PMID:15798202 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19064922 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20200310 MGI PMID:22096518 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002064 seizures IAGP N RGD:5509061 20200310 MGI PMID:12812988 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002064 seizures IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200310 MGI PMID:12812988 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200310 MGI PMID:22096518 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:12812988 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19064922 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:20364121 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:27297240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200423 MGI PMID:30858608 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:17418413 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200310 MGI PMID:15218525 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20200310 MGI PMID:20187849 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:8790342 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:16510575 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15265883 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15306694 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15561996 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15870264 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:17056592 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:18395839 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:18755891 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:24167636 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20231102 MGI PMID:24411735 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20221215 MGI PMID:25975378 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20200310 MGI PMID:24430185 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20200310 MGI PMID:22096518 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200310 MGI PMID:25100603 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:24430185 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20221215 MGI PMID:25975378 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20200310 MGI PMID:12944494 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20531296 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20200310 MGI PMID:23446734 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200310 MGI PMID:15798202 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002731 megacolon IAGP N RGD:5509061 20200310 MGI PMID:20187849 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20200310 MGI PMID:20187849 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:22926762 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20200310 MGI PMID:22290436 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20200310 MGI PMID:3221240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20200310 MGI PMID:12388794 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20200310 MGI PMID:15201433 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20200310 MGI PMID:10625648 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20200310 MGI PMID:12388794 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20200310 MGI PMID:20484117 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002872 polycythemia IAGP N RGD:5509061 20200310 MGI PMID:15798202 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20200310 MGI 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20221215 MGI PMID:25975378 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20200310 MGI PMID:24430185 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20200310 MGI PMID:22096518 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20200310 MGI PMID:19064922 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20200310 MGI PMID:20484117 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20200310 MGI PMID:24061480 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002969 impaired social transmission of food preference IAGP N RGD:5509061 20200310 MGI PMID:25100603 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20200310 MGI PMID:15306694 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20200310 MGI PMID:22733797 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:20364121 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:20364121 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20200310 MGI PMID:28683291 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:27297240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003171 phenotypic reversion IAGP N RGD:5509061 20200310 MGI PMID:2912572 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003228 abnormal sinus venosus morphology IAGP N RGD:5509061 20200310 MGI PMID:22926762 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:11297820 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:7509865 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20200310 MGI PMID:3221240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20200310 MGI PMID:20364121 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003350 increased circulating levels of thyroid hormone IAGP N RGD:5509061 20200310 MGI PMID:24265449 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200310 MGI PMID:25100603 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20200310 MGI PMID:23770692 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20200310 MGI PMID:22412863 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:19458618 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20200310 MGI PMID:22733797 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20200310 MGI PMID:20364121 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20200310 MGI PMID:25100603 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20221215 MGI PMID:25975378 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19064922 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:27895157 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:15306694 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:16510575 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20200310 MGI PMID:21930766 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20200310 MGI PMID:22733797 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:15218525 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:21930766 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:22412863 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20200310 MGI PMID:18037992 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20200310 MGI PMID:22733797 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20200310 MGI PMID:20360310 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20200310 MGI PMID:22412863 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20200310 MGI PMID:16461894 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20200310 MGI PMID:27895157 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20200310 MGI PMID:12812988 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20200310 MGI PMID:25100603 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20200310 MGI PMID:16461894 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004494 abnormal synaptic glutamate release IAGP N RGD:5509061 20200310 MGI PMID:24430185 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20200310 MGI PMID:24667635 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20200310 MGI PMID:22733797 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200310 MGI PMID:22290436 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20200310 MGI PMID:22096518 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:18037992 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:10953035 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20200310 MGI PMID:12944494 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:12944494 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005119 decreased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:24265449 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:16461894 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20200310 MGI PMID:27895157 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20200310 MGI PMID:18037992 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20200310 MGI PMID:24055366 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20200310 MGI PMID:27895157 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20200310 MGI PMID:20364121 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20200310 MGI PMID:22723298 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20200310 MGI PMID:20484117 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:24622775 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20200310 MGI PMID:16906226 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:20484117 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005424 jerky movement IAGP N RGD:5509061 20200310 MGI PMID:9413985 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20200310 MGI PMID:24265449 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20200310 MGI PMID:24265449 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20200310 MGI PMID:24265449 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20200310 MGI PMID:23446734 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20200310 MGI PMID:21459331 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20200310 MGI PMID:27895157 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:15798202 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20200310 MGI PMID:27895157 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005583 decreased renin activity IAGP N RGD:5509061 20200310 MGI PMID:15306694 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:15201433 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:16461894 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20200310 MGI PMID:3221240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20200310 MGI PMID:7509865 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20200310 MGI PMID:24055366 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20200310 MGI PMID:15798202 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20200310 MGI PMID:18945948 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20200310 MGI PMID:21459331 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19064922 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0006373 abnormal circulating angiotensinogen level IAGP N RGD:5509061 20200310 MGI PMID:18945948 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20200310 MGI PMID:20484117 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20200310 MGI PMID:20484117 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20200310 MGI PMID:20484117 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20200310 MGI PMID:24061480 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:23446734 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20200310 MGI PMID:27297240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008301 adrenal medulla hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:16906226 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20200310 MGI PMID:22096518 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20200310 MGI PMID:24430185 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20200310 MGI PMID:25100603 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20200310 MGI PMID:22096518 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20200310 MGI PMID:24430185 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20200310 MGI PMID:18945948 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20200310 MGI PMID:22290436 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20200310 MGI PMID:12944494 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:23770692 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:24667635 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20200310 MGI PMID:20364121 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20200310 MGI PMID:20364121 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200423 MGI PMID:30858608 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0009179 abnormal pancreatic alpha cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:20364121 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:19081794 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19081794 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:12944494 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20200310 MGI PMID:27297240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0009436 fragmentation of sleep/wake states IAGP N RGD:5509061 20200310 MGI PMID:22096518 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20200310 MGI PMID:19064922 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20200310 MGI PMID:20187849 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19064922 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0009845 abnormal neural crest cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20200310 MGI PMID:23770692 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:27297240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0010108 abnormal renal water reabsorption IAGP N RGD:5509061 20200310 MGI PMID:21459331 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20201231 MGI PMID:31932351 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20200310 MGI PMID:27895157 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19738070 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:17018605 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20200310 MGI PMID:28683291 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0010449 heart right ventricle outflow tract stenosis IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20200310 MGI PMID:22926762 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0010892 increased oligodendrocyte progenitor number IAGP N RGD:5509061 20201231 MGI PMID:31932351 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20200310 MGI PMID:28683291 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20187849 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22926762 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19064922 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17491588 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221215 MGI PMID:25975378 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19064922 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17418413 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22412863 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20080592 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21930766 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22926762 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16906226 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15218525 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22412863 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22723298 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22723298 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011262 abnormal pharyngeal arch mesenchyme morphology IAGP N RGD:5509061 20200310 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20200310 MGI PMID:20484117 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:22926762 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011426 abnormal ureter smooth muscle morphology IAGP N RGD:5509061 20200310 MGI PMID:20881014 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20200310 MGI PMID:20484117 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20200310 MGI PMID:25100603 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20200310 MGI PMID:24055366 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20240118 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0012006 abnormal hippocampus physiology IAGP N RGD:5509061 20200310 MGI PMID:27297240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20200310 MGI PMID:28683291 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20200310 MGI PMID:23770692 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200310 MGI PMID:27297240 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19064922 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0012592 decreased brain choline acetyltransferase activity IAGP N RGD:5509061 20200310 MGI PMID:7509865 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0012735 abnormal response to exercise IAGP N RGD:5509061 20200310 MGI PMID:28683291 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20200423 MGI PMID:30858608 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0014074 increased brain glycogen level IAGP N RGD:5509061 20200310 MGI PMID:24452334 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0014234 decreased enterocyte apoptosis IAGP N RGD:5509061 20230323 MGI PMID:24667635 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:22096518 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:25100603 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0020078 decreased brain tyrosine 3-monooxygenase activity IAGP N RGD:5509061 20200310 MGI PMID:7509865 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0020168 decreased thyroid gland weight IAGP N RGD:5509061 20200310 MGI PMID:24265449 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0020316 decreased vascular endothelial cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:19458618 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200310 MGI PMID:24452334 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0030971 ketoacidosis IAGP N RGD:5509061 20200310 MGI PMID:20364121 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0031232 increased circulating angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:18945948 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0031517 interrupted aortic arch, type c IAGP N RGD:5509061 20240118 MGI PMID:18058916 1549982 Hprt1 hypoxanthine phosphoribosyltransferase 1 gene MP:0031590 abnormal epicardium development IAGP N RGD:5509061 20240229 MGI PMID:22926762 1549983 Gkn1 gastrokine 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1549983 Gkn1 gastrokine 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1549983 Gkn1 gastrokine 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20201231 MGI 1549983 Gkn1 gastrokine 1 gene MP:0000458 abnormal mandible morphology IEA N RGD:5509061 20201231 MGI 1549983 Gkn1 gastrokine 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1549983 Gkn1 gastrokine 1 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1549983 Gkn1 gastrokine 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1549983 Gkn1 gastrokine 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1549986 Zkscan17 zinc finger with KRAB and SCAN domains 17 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1549986 Zkscan17 zinc finger with KRAB and SCAN domains 17 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1549986 Zkscan17 zinc finger with KRAB and SCAN domains 17 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1549987 Wdr19 WD repeat domain 19 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0000088 short mandible IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0000097 short maxilla IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0000111 cleft palate IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0000154 rib fusion IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0000413 polyphalangy IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0000568 ectopic digits IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0002728 absent tibia IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0004320 split sternum IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0004385 interparietal bone hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0004420 parietal bone hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0004443 absent supraoccipital bone IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0004672 short ribs IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0009895 decreased palatine bone horizontal plate size IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0011261 abnormal limb mesenchyme morphology IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0011685 abnormal limb paddle morphology IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0030066 short face IAGP N RGD:5509061 20200310 MGI PMID:22228095 1549987 Wdr19 WD repeat domain 19 gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:22228095 1549988 Tlr9 toll-like receptor 9 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16818796 1549988 Tlr9 toll-like receptor 9 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16818796 1549988 Tlr9 toll-like receptor 9 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17456769 1549988 Tlr9 toll-like receptor 9 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16818796 1549988 Tlr9 toll-like receptor 9 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:16818796 1549988 Tlr9 toll-like receptor 9 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11130078 1549988 Tlr9 toll-like receptor 9 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16818796 1549988 Tlr9 toll-like receptor 9 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21683627 1549988 Tlr9 toll-like receptor 9 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11130078 1549988 Tlr9 toll-like receptor 9 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14563635 1549988 Tlr9 toll-like receptor 9 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11130078 1549988 Tlr9 toll-like receptor 9 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:14993594 1549988 Tlr9 toll-like receptor 9 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17118979 1549988 Tlr9 toll-like receptor 9 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11130078 1549988 Tlr9 toll-like receptor 9 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16818796 1549988 Tlr9 toll-like receptor 9 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16818796 1549988 Tlr9 toll-like receptor 9 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:16818796 1549988 Tlr9 toll-like receptor 9 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:14993594 1549988 Tlr9 toll-like receptor 9 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:21458307 1549988 Tlr9 toll-like receptor 9 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21683627 1549988 Tlr9 toll-like receptor 9 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16440059 1549988 Tlr9 toll-like receptor 9 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16703567 1549988 Tlr9 toll-like receptor 9 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17456769 1549988 Tlr9 toll-like receptor 9 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17135446 1549988 Tlr9 toll-like receptor 9 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17389237 1549988 Tlr9 toll-like receptor 9 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16818796 1549988 Tlr9 toll-like receptor 9 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0005093 decreased B cell proliferation IEA N RGD:5509061 20111116 MGI 1549988 Tlr9 toll-like receptor 9 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:11130078 1549988 Tlr9 toll-like receptor 9 gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14993594 1549988 Tlr9 toll-like receptor 9 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16703567 1549988 Tlr9 toll-like receptor 9 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20111116 MGI 1549988 Tlr9 toll-like receptor 9 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17456769 1549988 Tlr9 toll-like receptor 9 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:17389237 1549988 Tlr9 toll-like receptor 9 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:17389237 1549988 Tlr9 toll-like receptor 9 gene MP:0008567 decreased interferon-gamma secretion IEA N RGD:5509061 20111116 MGI 1549988 Tlr9 toll-like receptor 9 gene MP:0008573 increased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:16461338 1549988 Tlr9 toll-like receptor 9 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:17389237 1549988 Tlr9 toll-like receptor 9 gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16973389 1549988 Tlr9 toll-like receptor 9 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14993594 1549988 Tlr9 toll-like receptor 9 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:16818796 1549988 Tlr9 toll-like receptor 9 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:14993594 1549988 Tlr9 toll-like receptor 9 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:14993594 1549990 Chat choline O-acetyltransferase gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12441053 1549990 Chat choline O-acetyltransferase gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12533614 1549990 Chat choline O-acetyltransferase gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19635813 1549990 Chat choline O-acetyltransferase gene MP:0000160 kyphosis IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:23374353 1549990 Chat choline O-acetyltransferase gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0000745 tremors IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:12879071 1549990 Chat choline O-acetyltransferase gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19635813 1549990 Chat choline O-acetyltransferase gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:12441053 1549990 Chat choline O-acetyltransferase gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20170223 MGI PMID:26842965 1549990 Chat choline O-acetyltransferase gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:19421194 1549990 Chat choline O-acetyltransferase gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:19635813 1549990 Chat choline O-acetyltransferase gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:12441053 1549990 Chat choline O-acetyltransferase gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:12879071 1549990 Chat choline O-acetyltransferase gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:12441053 1549990 Chat choline O-acetyltransferase gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:12533614 1549990 Chat choline O-acetyltransferase gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:12879071 1549990 Chat choline O-acetyltransferase gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:19635813 1549990 Chat choline O-acetyltransferase gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:19726636 1549990 Chat choline O-acetyltransferase gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20170223 MGI PMID:26842965 1549990 Chat choline O-acetyltransferase gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20230914 MGI PMID:35767949 1549990 Chat choline O-acetyltransferase gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12441053 1549990 Chat choline O-acetyltransferase gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12441053 1549990 Chat choline O-acetyltransferase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21423695 1549990 Chat choline O-acetyltransferase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19635813 1549990 Chat choline O-acetyltransferase gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20171221 MGI PMID:28159985 1549990 Chat choline O-acetyltransferase gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20170420 MGI PMID:27810937 1549990 Chat choline O-acetyltransferase gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20170420 MGI PMID:27810937 1549990 Chat choline O-acetyltransferase gene MP:0001957 apnea IAGP N RGD:5509061 20170420 MGI PMID:27810937 1549990 Chat choline O-acetyltransferase gene MP:0001957 apnea IAGP N RGD:5509061 20171221 MGI PMID:28159985 1549990 Chat choline O-acetyltransferase gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23374353 1549990 Chat choline O-acetyltransferase gene MP:0002083 premature death IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0002083 premature death IAGP N RGD:5509061 20171221 MGI PMID:28159985 1549990 Chat choline O-acetyltransferase gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12441053 1549990 Chat choline O-acetyltransferase gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19116659 1549990 Chat choline O-acetyltransferase gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:12533614 1549990 Chat choline O-acetyltransferase gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23374353 1549990 Chat choline O-acetyltransferase gene MP:0002337 abnormal whole-body plethysmography IAGP N RGD:5509061 20170420 MGI PMID:27810937 1549990 Chat choline O-acetyltransferase gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:21423695 1549990 Chat choline O-acetyltransferase gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20230914 MGI PMID:35767949 1549990 Chat choline O-acetyltransferase gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12533614 1549990 Chat choline O-acetyltransferase gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:24179230 1549990 Chat choline O-acetyltransferase gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20171221 MGI PMID:28159985 1549990 Chat choline O-acetyltransferase gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24179230 1549990 Chat choline O-acetyltransferase gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:12441053 1549990 Chat choline O-acetyltransferase gene MP:0003928 increased heart rate variability IAGP N RGD:5509061 20171221 MGI PMID:28159985 1549990 Chat choline O-acetyltransferase gene MP:0004085 abnormal heartbeat IAGP N RGD:5509061 20171221 MGI PMID:28159985 1549990 Chat choline O-acetyltransferase gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:19635813 1549990 Chat choline O-acetyltransferase gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:12533614 1549990 Chat choline O-acetyltransferase gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20171221 MGI PMID:28159985 1549990 Chat choline O-acetyltransferase gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:19635813 1549990 Chat choline O-acetyltransferase gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:21423695 1549990 Chat choline O-acetyltransferase gene MP:0004836 abnormal synaptic acetylcholine release IAGP N RGD:5509061 20141003 MGI PMID:19635813 1549990 Chat choline O-acetyltransferase gene MP:0005162 carpoptosis IAGP N RGD:5509061 20141003 MGI PMID:12441053 1549990 Chat choline O-acetyltransferase gene MP:0005162 carpoptosis IAGP N RGD:5509061 20141003 MGI PMID:12533614 1549990 Chat choline O-acetyltransferase gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:12441053 1549990 Chat choline O-acetyltransferase gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:12533614 1549990 Chat choline O-acetyltransferase gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19635813 1549990 Chat choline O-acetyltransferase gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:20498043 1549990 Chat choline O-acetyltransferase gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24179230 1549990 Chat choline O-acetyltransferase gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20171221 MGI PMID:28159985 1549990 Chat choline O-acetyltransferase gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:12879071 1549990 Chat choline O-acetyltransferase gene MP:0005507 tail dragging IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20171221 MGI PMID:28159985 1549990 Chat choline O-acetyltransferase gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20170420 MGI PMID:27810937 1549990 Chat choline O-acetyltransferase gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:24179230 1549990 Chat choline O-acetyltransferase gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20171221 MGI PMID:28159985 1549990 Chat choline O-acetyltransferase gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:19635813 1549990 Chat choline O-acetyltransferase gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:19635813 1549990 Chat choline O-acetyltransferase gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141218 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0009420 skeletal muscle endomysial fibrosis IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20171221 MGI PMID:28159985 1549990 Chat choline O-acetyltransferase gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20230914 MGI PMID:35767949 1549990 Chat choline O-acetyltransferase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12879071 1549990 Chat choline O-acetyltransferase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12441053 1549990 Chat choline O-acetyltransferase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19635813 1549990 Chat choline O-acetyltransferase gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12533614 1549990 Chat choline O-acetyltransferase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20230914 MGI PMID:35767949 1549990 Chat choline O-acetyltransferase gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20141016 MGI PMID:24486622 1549990 Chat choline O-acetyltransferase gene MP:0012593 increased brain choline acetyltransferase activity IAGP N RGD:5509061 20170420 MGI PMID:27810937 1549990 Chat choline O-acetyltransferase gene MP:0030676 increased acetylcholine level IAGP N RGD:5509061 20180927 MGI PMID:19635813 1549990 Chat choline O-acetyltransferase gene MP:0030676 increased acetylcholine level IAGP N RGD:5509061 20180927 MGI PMID:27810937 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0001433 polyphagia IAGP N RGD:5509061 20170907 MGI PMID:27133129 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20170907 MGI PMID:27133129 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0002626 increased heart rate IAGP N RGD:5509061 20180301 MGI PMID:29097735 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20170907 MGI PMID:27133129 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20170907 MGI PMID:27133129 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20170907 MGI PMID:27133129 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20170907 MGI PMID:27133129 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0004115 abnormal sinoatrial node morphology IAGP N RGD:5509061 20180301 MGI PMID:29097735 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20180301 MGI PMID:29097735 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20170907 MGI PMID:27133129 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0005331 insulin resistance IAGP N RGD:5509061 20170907 MGI PMID:27133129 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20180301 MGI PMID:29097735 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20180301 MGI PMID:29097735 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20170907 MGI PMID:27133129 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20180301 MGI PMID:29097735 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20180301 MGI PMID:29097735 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20170907 MGI PMID:27133129 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210520 MGI 1549995 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240321 MGI PMID:27133129 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000376 folliculitis IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000414 alopecia IEA N RGD:5509061 20200310 MGI 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000765 abnormal tongue squamous epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0000997 abnormal synovial joint capsule morphology IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001190 reddish skin IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001190 reddish skin IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001192 scaly skin IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001192 scaly skin IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001194 dermatitis IAGP N RGD:5509061 20200310 MGI PMID:17538631 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001194 dermatitis IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001212 skin lesions IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001212 skin lesions IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001219 thick epidermis IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001219 thick epidermis IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001786 skin edema IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001874 acanthosis IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:17538631 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0002220 large lymphoid organs IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20200310 MGI PMID:17538631 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20200310 MGI PMID:17538631 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0002933 joint inflammation IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0003278 esophageal inflammation IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0003427 parakeratosis IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0003427 parakeratosis IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0003865 lymph node inflammation IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0004947 skin inflammation IAGP N RGD:5509061 20200310 MGI PMID:17538631 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0005114 premature hair loss IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0005114 premature hair loss IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0006162 thick eyelids IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0008463 abnormal peripheral lymph node morphology IAGP N RGD:5509061 20200618 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20200310 MGI PMID:17538631 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0009715 thick epidermis stratum basale IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0010072 increased pruritus IAGP N RGD:5509061 20200310 MGI PMID:8774148 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0014349 absent spleen B cell follicles IAGP N RGD:5509061 20240104 MGI PMID:10201907 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0014349 absent spleen B cell follicles IAGP N RGD:5509061 20240104 MGI PMID:17538631 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0031395 cutaneous mastocytosis IAGP N RGD:5509061 20220721 MGI PMID:8362989 1549996 Sharpin SHANK-associated RH domain interacting protein gene MP:0031395 cutaneous mastocytosis IAGP N RGD:5509061 20220721 MGI PMID:8774148 1549997 Prss3b protease, serine 3B gene MP:0001265 decreased body size IAGP N RGD:5509061 20190620 MGI PMID:30487519 1549997 Prss3b protease, serine 3B gene MP:0001399 hyperactivity IEA N RGD:5509061 20230720 MGI 1549997 Prss3b protease, serine 3B gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20190620 MGI PMID:30487519 1549997 Prss3b protease, serine 3B gene MP:0002083 premature death IAGP N RGD:5509061 20190620 MGI PMID:30487519 1549997 Prss3b protease, serine 3B gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230720 MGI 1549997 Prss3b protease, serine 3B gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20230720 MGI 1549997 Prss3b protease, serine 3B gene MP:0003340 acute pancreas inflammation IAGP N RGD:5509061 20190620 MGI PMID:30487519 1549997 Prss3b protease, serine 3B gene MP:0003341 chronic pancreas inflammation IAGP N RGD:5509061 20190620 MGI PMID:30487519 1549997 Prss3b protease, serine 3B gene MP:0004247 small pancreas IAGP N RGD:5509061 20190620 MGI PMID:30487519 1549997 Prss3b protease, serine 3B gene MP:0008805 decreased circulating amylase level IAGP N RGD:5509061 20190620 MGI PMID:30487519 1549997 Prss3b protease, serine 3B gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20190620 MGI PMID:30487519 1549997 Prss3b protease, serine 3B gene MP:0009109 decreased pancreas weight IAGP N RGD:5509061 20190620 MGI PMID:30487519 1549997 Prss3b protease, serine 3B gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230720 MGI 1549997 Prss3b protease, serine 3B gene MP:0009149 decreased pancreatic acinar cell number IAGP N RGD:5509061 20190620 MGI PMID:30487519 1549997 Prss3b protease, serine 3B gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20190620 MGI PMID:30487519 1549997 Prss3b protease, serine 3B gene MP:0013295 pancreas atrophy IAGP N RGD:5509061 20190620 MGI PMID:30487519 1549998 C1rl complement component 1, r subcomponent-like gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20160421 MGI 1549998 C1rl complement component 1, r subcomponent-like gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20160421 MGI 1549998 C1rl complement component 1, r subcomponent-like gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210520 MGI 1549998 C1rl complement component 1, r subcomponent-like gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20201231 MGI 1549999 Atp6v1e1 ATPase, H+ transporting, lysosomal V1 subunit E1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550001 Alpk1 alpha-kinase 1 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20240404 MGI PMID:35868845 1550001 Alpk1 alpha-kinase 1 gene MP:0031220 increased circulating CXCL10 level IAGP N RGD:5509061 20240404 MGI PMID:35868845 1550002 Prmt6 protein arginine N-methyltransferase 6 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:22904064 1550002 Prmt6 protein arginine N-methyltransferase 6 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20200310 MGI PMID:22904064 1550002 Prmt6 protein arginine N-methyltransferase 6 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:22904064 1550004 Spred3 sprouty-related EVH1 domain containing 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20200310 MGI 1550004 Spred3 sprouty-related EVH1 domain containing 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20200310 MGI 1550004 Spred3 sprouty-related EVH1 domain containing 3 gene MP:0002989 small kidney IEA N RGD:5509061 20200310 MGI 1550004 Spred3 sprouty-related EVH1 domain containing 3 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20200310 MGI 1550004 Spred3 sprouty-related EVH1 domain containing 3 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1550004 Spred3 sprouty-related EVH1 domain containing 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1550004 Spred3 sprouty-related EVH1 domain containing 3 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20220519 MGI 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0004265 abnormal placental transport IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0011653 decreased circulating histidine level IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0012172 abnormal amniotic fluid composition IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0030668 decreased circulating proline level IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0030674 decreased circulating alanine level IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550006 Slc43a2 solute carrier family 43, member 2 gene MP:0030695 decreased circulating serine level IAGP N RGD:5509061 20200310 MGI PMID:25480797 1550007 Wipi2 WD repeat domain, phosphoinositide interacting 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1550008 Tinagl1 tubulointerstitial nephritis antigen-like 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:26522507 1550008 Tinagl1 tubulointerstitial nephritis antigen-like 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:26522507 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20210506 MGI PMID:33552067 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15496441 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:12361967 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:24415953 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:15496441 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:16571625 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:16571625 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:16571625 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15496441 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15496441 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12361967 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:14723851 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:14723851 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:14723851 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:14723851 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18691547 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12385751 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20231012 MGI PMID:37334372 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20231012 MGI PMID:37334372 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0003126 abnormal external female genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:19282366 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0003553 abnormal foreskin morphology IAGP N RGD:5509061 20141003 MGI PMID:19282366 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:12361967 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20141003 MGI PMID:19282366 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0004711 persistence of notochord tissue IAGP N RGD:5509061 20141003 MGI PMID:12361967 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:14723851 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0004979 abnormal neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:14723851 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0005315 absent pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:15496441 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18691547 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20231012 MGI PMID:37334372 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20231012 MGI PMID:37334372 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0009199 abnormal external male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0009199 abnormal external male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:19282366 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0009569 abnormal left lung morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0009571 abnormal right lung accessory lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0009572 abnormal right lung cranial lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:14723851 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20231012 MGI PMID:37334372 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0011011 impaired lung lobe morphogenesis IAGP N RGD:5509061 20200917 MGI PMID:12361967 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12361967 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10725236 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0021101 abnormal ventral interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:14723851 1550011 Gli1 GLI-Kruppel family member GLI1 gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:14723851 1550015 Epdr1 ependymin related 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1550015 Epdr1 ependymin related 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20170105 MGI 1550015 Epdr1 ependymin related 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20221215 MGI 1550015 Epdr1 ependymin related 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1550015 Epdr1 ependymin related 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1550016 Ust uronyl-2-sulfotransferase gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1550016 Ust uronyl-2-sulfotransferase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1550017 Prkcb protein kinase C, beta gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20200310 MGI PMID:10934237 1550017 Prkcb protein kinase C, beta gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20200310 MGI PMID:10934237 1550017 Prkcb protein kinase C, beta gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20200310 MGI PMID:23552399 1550017 Prkcb protein kinase C, beta gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20200310 MGI PMID:8670417 1550017 Prkcb protein kinase C, beta gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20200310 MGI PMID:22761313 1550017 Prkcb protein kinase C, beta gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20200310 MGI PMID:23552399 1550017 Prkcb protein kinase C, beta gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20200310 MGI PMID:8670417 1550017 Prkcb protein kinase C, beta gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20200310 MGI PMID:15662033 1550017 Prkcb protein kinase C, beta gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20200310 MGI PMID:8670417 1550017 Prkcb protein kinase C, beta gene MP:0005015 increased T cell number IEA N RGD:5509061 20200310 MGI 1550017 Prkcb protein kinase C, beta gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:8670417 1550017 Prkcb protein kinase C, beta gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:23552399 1550017 Prkcb protein kinase C, beta gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:8670417 1550017 Prkcb protein kinase C, beta gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1550017 Prkcb protein kinase C, beta gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1550017 Prkcb protein kinase C, beta gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20200310 MGI PMID:23552399 1550017 Prkcb protein kinase C, beta gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20200310 MGI PMID:8670417 1550017 Prkcb protein kinase C, beta gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20200310 MGI PMID:23552399 1550017 Prkcb protein kinase C, beta gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20200310 MGI PMID:8670417 1550017 Prkcb protein kinase C, beta gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20200310 MGI 1550017 Prkcb protein kinase C, beta gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20200310 MGI 1550019 Pi16 peptidase inhibitor 16 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20231207 MGI 1550019 Pi16 peptidase inhibitor 16 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1550019 Pi16 peptidase inhibitor 16 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1550019 Pi16 peptidase inhibitor 16 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1550019 Pi16 peptidase inhibitor 16 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 1550019 Pi16 peptidase inhibitor 16 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 1550019 Pi16 peptidase inhibitor 16 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20200310 MGI PMID:27539859 1550019 Pi16 peptidase inhibitor 16 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20200310 MGI PMID:27539859 1550019 Pi16 peptidase inhibitor 16 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1550019 Pi16 peptidase inhibitor 16 gene MP:0002344 abnormal lymph node B cell domain morphology IEA N RGD:5509061 20200310 MGI 1550019 Pi16 peptidase inhibitor 16 gene MP:0002359 abnormal spleen germinal center morphology IEA N RGD:5509061 20200310 MGI 1550019 Pi16 peptidase inhibitor 16 gene MP:0002397 abnormal bone marrow morphology IEA N RGD:5509061 20200310 MGI 1550019 Pi16 peptidase inhibitor 16 gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 1550019 Pi16 peptidase inhibitor 16 gene MP:0004973 increased regulatory T cell number IEA N RGD:5509061 20200310 MGI 1550019 Pi16 peptidase inhibitor 16 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20231207 MGI 1550021 Sucnr1 succinate receptor 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18820681 1550021 Sucnr1 succinate receptor 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:18535668 1550021 Sucnr1 succinate receptor 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18820681 1550021 Sucnr1 succinate receptor 1 gene MP:0003353 decreased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:18535668 1550021 Sucnr1 succinate receptor 1 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:18820681 1550021 Sucnr1 succinate receptor 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18820681 1550021 Sucnr1 succinate receptor 1 gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18820681 1550021 Sucnr1 succinate receptor 1 gene MP:0008686 abnormal interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:18820681 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20160623 MGI PMID:26763459 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0000678 abnormal parathyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17694176 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:16847339 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9391157 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9391157 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:11689889 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0001562 abnormal circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:11438569 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16847339 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12077299 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16847339 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:16847339 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:9391157 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002249 abnormal larynx morphology IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11826096 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17482476 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:11689889 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11689889 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18084302 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002876 abnormal thyroid gland physiology IAGP N RGD:5509061 20141003 MGI PMID:17694176 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:11826096 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0002985 abnormal urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:18084302 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:19171764 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20141003 MGI PMID:11826096 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:17694176 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:16847339 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:16847339 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:11689889 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0004697 abnormal thyroid follicular cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17694176 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18084302 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20161027 MGI PMID:26168216 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17694176 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20141003 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:12533510 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005409 darkened coat color IAGP N RGD:5509061 20160623 MGI PMID:26763459 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:12586747 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:9296496 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:17694176 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20161027 MGI PMID:26168216 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:19171764 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:9296496 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0009385 abnormal dermal pigmentation IAGP N RGD:5509061 20160623 MGI PMID:26763459 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0009387 abnormal epidermal pigmentation IAGP N RGD:5509061 20160623 MGI PMID:26763459 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:15774906 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0010326 malleus hypoplasia IAGP N RGD:5509061 20170928 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0010432 common ventricle IAGP N RGD:5509061 20141003 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0010640 ventricular myocardium compact layer hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11689889 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9296496 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9391157 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11689889 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12077299 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20160623 MGI PMID:26763459 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20160623 MGI PMID:26763459 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0012045 increased susceptibility to hypertension IAGP N RGD:5509061 20161027 MGI PMID:26168216 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0020106 decreased nitrate level IAGP N RGD:5509061 20161027 MGI PMID:26168216 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:16988000 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0030107 incus hypoplasia IAGP N RGD:5509061 20170928 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0030128 stapes hypoplasia IAGP N RGD:5509061 20170928 MGI PMID:9687499 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0030299 lower jaw to upper jaw transformation IAGP N RGD:5509061 20171102 MGI PMID:18199583 1550022 Gnaq guanine nucleotide binding protein, alpha q polypeptide gene MP:0030884 rachitic rosary IAGP N RGD:5509061 20181101 MGI PMID:16988000 1550026 Popdc2 popeye domain containing 2 gene MP:0004115 abnormal sinoatrial node morphology IAGP N RGD:5509061 20141003 MGI PMID:22354168 1550026 Popdc2 popeye domain containing 2 gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:22354168 1550026 Popdc2 popeye domain containing 2 gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:22354168 1550026 Popdc2 popeye domain containing 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:22354168 1550026 Popdc2 popeye domain containing 2 gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20141003 MGI PMID:22354168 1550027 Khdrbs3 KH domain containing, RNA binding, signal transduction associated 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1550027 Khdrbs3 KH domain containing, RNA binding, signal transduction associated 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23637638 1550027 Khdrbs3 KH domain containing, RNA binding, signal transduction associated 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0000601 small liver IEA N RGD:5509061 20230119 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0000692 small spleen IEA N RGD:5509061 20230119 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0000774 decreased brain size IEA N RGD:5509061 20230119 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0001147 small testis IEA N RGD:5509061 20230119 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230119 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0002175 decreased brain weight IEA N RGD:5509061 20231207 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230119 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230119 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0009453 enhanced contextual conditioning behavior IEA N RGD:5509061 20231207 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0009455 enhanced cued conditioning behavior IEA N RGD:5509061 20231207 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20231207 MGI 1550028 Ubqln4 ubiquilin 4 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1550029 Fbxo42 F-box protein 42 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20240523 MGI 1550029 Fbxo42 F-box protein 42 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1550029 Fbxo42 F-box protein 42 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20230601 MGI 1550029 Fbxo42 F-box protein 42 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 1550029 Fbxo42 F-box protein 42 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1550029 Fbxo42 F-box protein 42 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20240523 MGI 1550029 Fbxo42 F-box protein 42 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20230601 MGI 1550029 Fbxo42 F-box protein 42 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1550033 Azin1 antizyme inhibitor 1 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20200310 MGI PMID:19077035 1550033 Azin1 antizyme inhibitor 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20200310 MGI PMID:19077035 1550033 Azin1 antizyme inhibitor 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19077035 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14966563 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:12105862 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0000597 delayed hepatic development IAGP N RGD:5509061 20141003 MGI PMID:12105862 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11121396 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12105862 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0002090 abnormal vision IAGP N RGD:5509061 20200116 MGI PMID:27147662 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12105862 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14966563 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:12105862 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20200116 MGI PMID:27147662 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200116 MGI PMID:27147662 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11121396 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12105862 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0011877 absent liver IAGP N RGD:5509061 20141003 MGI PMID:12105862 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200116 MGI PMID:27147662 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:27147662 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:27147662 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0012235 abnormal liver bud morphology IAGP N RGD:5509061 20141003 MGI PMID:12105862 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0012504 increased forebrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12105862 1550037 Icmt isoprenylcysteine carboxyl methyltransferase gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12105862 1550043 Gjd4 gap junction protein, delta 4 gene MP:0000730 increased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:21272575 1550043 Gjd4 gap junction protein, delta 4 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:21272575 1550043 Gjd4 gap junction protein, delta 4 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20201022 MGI 1550043 Gjd4 gap junction protein, delta 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 1550043 Gjd4 gap junction protein, delta 4 gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:21272575 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:11847113 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11847113 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:11847113 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11847113 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11847113 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21685933 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11847113 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0003794 delayed somite formation IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0004653 absent caudal vertebrae IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:11847113 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21685933 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11847113 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550045 Tacc3 transforming, acidic coiled-coil containing protein 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17359303 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210128 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20201022 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20170629 MGI PMID:27555298 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20201022 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20170629 MGI PMID:27555298 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20170629 MGI PMID:27555298 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20201022 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20170629 MGI PMID:27555298 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20170629 MGI PMID:27555298 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240627 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20170629 MGI PMID:27555298 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20210520 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20170629 MGI PMID:27555298 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20170629 MGI PMID:27555298 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20170629 MGI PMID:27555298 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20170629 MGI PMID:27555298 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20170629 MGI PMID:27555298 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20170629 MGI PMID:27555298 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20170629 MGI PMID:27555298 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20210128 MGI 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20170629 MGI PMID:27555298 1550047 C1qtnf1 C1q and tumor necrosis factor related protein 1 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20170629 MGI PMID:27555298 1550049 Pir pirin gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20111116 MGI 1550050 Elavl3 ELAV like RNA binding protein 3 gene MP:0000948 nonconvulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:22998874 1550050 Elavl3 ELAV like RNA binding protein 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22998874 1550050 Elavl3 ELAV like RNA binding protein 3 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:22998874 1550050 Elavl3 ELAV like RNA binding protein 3 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:22998874 1550050 Elavl3 ELAV like RNA binding protein 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22998874 1550050 Elavl3 ELAV like RNA binding protein 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22998874 1550050 Elavl3 ELAV like RNA binding protein 3 gene MP:0030737 decreased glutamic acid level IAGP N RGD:5509061 20180927 MGI PMID:22998874 1550051 Cox7b cytochrome c oxidase subunit 7B gene MP:0009781 abnormal preimplantation embryo development IEA N RGD:5509061 20141016 MGI 1550052 Znhit2 zinc finger, HIT domain containing 2 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1550052 Znhit2 zinc finger, HIT domain containing 2 gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20241031 MGI PMID:39194072 1550052 Znhit2 zinc finger, HIT domain containing 2 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20241031 MGI PMID:39194072 1550052 Znhit2 zinc finger, HIT domain containing 2 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20241031 MGI PMID:39194072 1550052 Znhit2 zinc finger, HIT domain containing 2 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20241031 MGI PMID:39194072 1550052 Znhit2 zinc finger, HIT domain containing 2 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20241031 MGI PMID:39194072 1550052 Znhit2 zinc finger, HIT domain containing 2 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1550052 Znhit2 zinc finger, HIT domain containing 2 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1550052 Znhit2 zinc finger, HIT domain containing 2 gene MP:0008527 embryonic lethality at implantation IAGP N RGD:5509061 20241031 MGI PMID:39194072 1550052 Znhit2 zinc finger, HIT domain containing 2 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20241031 MGI PMID:39194072 1550052 Znhit2 zinc finger, HIT domain containing 2 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20241031 MGI PMID:39194072 1550052 Znhit2 zinc finger, HIT domain containing 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220519 MGI 1550052 Znhit2 zinc finger, HIT domain containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1550052 Znhit2 zinc finger, HIT domain containing 2 gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20241031 MGI PMID:39194072 1550052 Znhit2 zinc finger, HIT domain containing 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000264 failure of vascular branching IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000264 failure of vascular branching IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15085193 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15085193 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170209 MGI 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15085193 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20170209 MGI 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15085193 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0001619 abnormal vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:15085193 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15085193 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15085193 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15085193 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15085193 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15085193 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0003542 abnormal vascular endothelial cell development IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:15085193 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0004056 abnormal myocardium compact layer morphology IEA N RGD:5509061 20170209 MGI 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:15085193 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:15085193 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:15085193 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20170209 MGI 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20170209 MGI 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20170209 MGI 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170209 MGI 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12093914 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15085193 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20170209 MGI 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0012252 abnormal septum transversum morphology IAGP N RGD:5509061 20141003 MGI PMID:14675480 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12221099 1550055 Mapk7 mitogen-activated protein kinase 7 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16710360 1550058 Adgra3 adhesion G protein-coupled receptor A3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:17882221 1550059 Stxbp5 syntaxin binding protein 5 (tomosyn) gene MP:0001406 abnormal gait IEA N RGD:5509061 20201022 MGI 1550059 Stxbp5 syntaxin binding protein 5 (tomosyn) gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1550059 Stxbp5 syntaxin binding protein 5 (tomosyn) gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1550059 Stxbp5 syntaxin binding protein 5 (tomosyn) gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18936251 1550059 Stxbp5 syntaxin binding protein 5 (tomosyn) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:18936251 1550059 Stxbp5 syntaxin binding protein 5 (tomosyn) gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:18936251 1550059 Stxbp5 syntaxin binding protein 5 (tomosyn) gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18936251 1550059 Stxbp5 syntaxin binding protein 5 (tomosyn) gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18936251 1550059 Stxbp5 syntaxin binding protein 5 (tomosyn) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1550059 Stxbp5 syntaxin binding protein 5 (tomosyn) gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18936251 1550061 Calr calreticulin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17112388 1550061 Calr calreticulin gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10085286 1550061 Calr calreticulin gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10739657 1550061 Calr calreticulin gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:17112388 1550061 Calr calreticulin gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10085286 1550061 Calr calreticulin gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10739657 1550061 Calr calreticulin gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17112388 1550061 Calr calreticulin gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10739657 1550061 Calr calreticulin gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:10739657 1550061 Calr calreticulin gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20240530 MGI PMID:26388295 1550061 Calr calreticulin gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20240530 MGI PMID:26388295 1550061 Calr calreticulin gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20240530 MGI PMID:26388295 1550061 Calr calreticulin gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20240530 MGI PMID:26388295 1550061 Calr calreticulin gene MP:0001935 decreased litter size IAGP N RGD:5509061 20240530 MGI PMID:26388295 1550061 Calr calreticulin gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:17112388 1550061 Calr calreticulin gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20240530 MGI PMID:26388295 1550061 Calr calreticulin gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20240530 MGI PMID:26388295 1550061 Calr calreticulin gene MP:0002952 ventricular cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:10739657 1550061 Calr calreticulin gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:10085286 1550061 Calr calreticulin gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:10739657 1550061 Calr calreticulin gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:10739657 1550061 Calr calreticulin gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10739657 1550061 Calr calreticulin gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:9126744 1550061 Calr calreticulin gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:10085286 1550061 Calr calreticulin gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:17112388 1550061 Calr calreticulin gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:17112388 1550061 Calr calreticulin gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10085286 1550061 Calr calreticulin gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:17112388 1550061 Calr calreticulin gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20240530 MGI PMID:26388295 1550061 Calr calreticulin gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10739657 1550061 Calr calreticulin gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:17112388 1550061 Calr calreticulin gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20240530 MGI PMID:26388295 1550061 Calr calreticulin gene MP:0010498 abnormal interventricular septum muscular part morphology IAGP N RGD:5509061 20141003 MGI PMID:10739657 1550061 Calr calreticulin gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10739657 1550061 Calr calreticulin gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10085286 1550061 Calr calreticulin gene MP:0011128 increased tertiary ovarian follicle number IAGP N RGD:5509061 20240530 MGI PMID:26388295 1550061 Calr calreticulin gene MP:0011701 decreased cumulus expansion IAGP N RGD:5509061 20240530 MGI PMID:26388295 1550061 Calr calreticulin gene MP:0013283 failure of ventral body wall closure IAGP N RGD:5509061 20141003 MGI PMID:10739657 1550061 Calr calreticulin gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20160310 MGI PMID:17112388 1550061 Calr calreticulin gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20240530 MGI PMID:26388295 1550061 Calr calreticulin gene MP:0031018 decreased granulosa cell proliferation IAGP N RGD:5509061 20240530 MGI PMID:26388295 1550061 Calr calreticulin gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20240530 MGI PMID:26388295 1550062 Ddah2 DDAH family member 2, ADMA independent gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550062 Ddah2 DDAH family member 2, ADMA independent gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1550064 Tuba1a tubulin, alpha 1A gene MP:0000111 cleft palate IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22101068 1550064 Tuba1a tubulin, alpha 1A gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 1550064 Tuba1a tubulin, alpha 1A gene MP:0001785 edema IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0001914 hemorrhage IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22101068 1550064 Tuba1a tubulin, alpha 1A gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:22101068 1550064 Tuba1a tubulin, alpha 1A gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20230601 MGI 1550064 Tuba1a tubulin, alpha 1A gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0004631 abnormal auditory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0004979 abnormal neuronal precursor cell number IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22101068 1550064 Tuba1a tubulin, alpha 1A gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22101068 1550064 Tuba1a tubulin, alpha 1A gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:17218254 1550064 Tuba1a tubulin, alpha 1A gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1550064 Tuba1a tubulin, alpha 1A gene MP:0014557 increased cortical ventricular zone thickness IAGP N RGD:5509061 20241031 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0020393 increased neuronal precursor proliferation IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20210304 MGI PMID:31386652 1550064 Tuba1a tubulin, alpha 1A gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22101068 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20200310 MGI PMID:21403399 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0000373 belly spot IAGP N RGD:5509061 20200310 MGI PMID:21403399 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:21572435 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:21403399 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:21403399 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21403399 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20200310 MGI PMID:21403399 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21403399 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21403399 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20200310 MGI PMID:21403399 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20200310 MGI PMID:21572435 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0004478 increased testicular teratoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21403399 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:21572435 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21572435 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0009222 increased uterus tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21403399 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21403399 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21403399 1550065 Cop1 COP1, E3 ubiquitin ligase gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21403399 1550066 Rfc1 replication factor C (activator 1) 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160421 MGI 1550066 Rfc1 replication factor C (activator 1) 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1550066 Rfc1 replication factor C (activator 1) 1 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20160811 MGI 1550066 Rfc1 replication factor C (activator 1) 1 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20210826 MGI 1550066 Rfc1 replication factor C (activator 1) 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1550066 Rfc1 replication factor C (activator 1) 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1550066 Rfc1 replication factor C (activator 1) 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1550066 Rfc1 replication factor C (activator 1) 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550066 Rfc1 replication factor C (activator 1) 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1550067 Lrp12 low density lipoprotein-related protein 12 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240627 MGI 1550067 Lrp12 low density lipoprotein-related protein 12 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20230817 MGI PMID:37330909 1550067 Lrp12 low density lipoprotein-related protein 12 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20230817 MGI PMID:37330909 1550067 Lrp12 low density lipoprotein-related protein 12 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20230817 MGI PMID:37330909 1550067 Lrp12 low density lipoprotein-related protein 12 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 1550067 Lrp12 low density lipoprotein-related protein 12 gene MP:0011804 increased cell migration IAGP N RGD:5509061 20230817 MGI PMID:37330909 1550067 Lrp12 low density lipoprotein-related protein 12 gene MP:0020213 enhanced leukocyte migration IAGP N RGD:5509061 20230817 MGI PMID:37330909 1550070 Srsf6 serine and arginine-rich splicing factor 6 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1550070 Srsf6 serine and arginine-rich splicing factor 6 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1550070 Srsf6 serine and arginine-rich splicing factor 6 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1550070 Srsf6 serine and arginine-rich splicing factor 6 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1550071 Mtg2 mitochondrial ribosome associated GTPase 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1550071 Mtg2 mitochondrial ribosome associated GTPase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550071 Mtg2 mitochondrial ribosome associated GTPase 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1550072 Tssk2 testis-specific serine kinase 2 gene MP:0001925 male infertility IEA N RGD:5509061 20240523 MGI 1550076 Lars1 leucyl-tRNA synthetase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1550077 Sil1 SIL1 nucleotide exchange factor gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16116427 1550077 Sil1 SIL1 nucleotide exchange factor gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19801575 1550077 Sil1 SIL1 nucleotide exchange factor gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16116427 1550077 Sil1 SIL1 nucleotide exchange factor gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19801575 1550077 Sil1 SIL1 nucleotide exchange factor gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16116427 1550077 Sil1 SIL1 nucleotide exchange factor gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19801575 1550077 Sil1 SIL1 nucleotide exchange factor gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:19801575 1550077 Sil1 SIL1 nucleotide exchange factor gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16116427 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:12874121 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000033 absent scala media IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:12874121 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20221215 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210520 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20201022 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:12783782 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:22945933 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:22945933 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15955062 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12874121 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16938278 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001512 trunk curl IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20201022 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:22945933 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002235 abnormal external nares morphology IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22340499 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002659 pituitary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002729 abnormal inner ear canal morphology IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0002990 short ureter IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210826 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003108 short zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003142 anotia IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003147 absent cochlea IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:16916509 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:16916509 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003164 decreased posterior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:16916509 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003166 decreased superior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:16916509 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16938278 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210128 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003358 abnormal hypaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003358 abnormal hypaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003358 abnormal hypaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12783782 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:12783782 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:16938278 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004161 cervical aortic arch IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004248 abnormal epaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004248 abnormal epaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004313 absent vestibulocochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004314 absent inner ear vestibule IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004317 small vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:16916509 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004317 small vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004318 absent incus IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004336 small utricle IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004422 small temporal bone IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004666 absent stapedial artery IAGP N RGD:5509061 20141003 MGI PMID:12874121 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004699 unilateral deafness IAGP N RGD:5509061 20141003 MGI PMID:12874121 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12874121 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004873 absent turbinates IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004922 abnormal common crus morphology IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12783782 1550080 Six1 sine oculis-related homeobox 1 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:12874121 1550080 Six1 sine oculis-related homeobox 1 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0005247 abnormal extraocular muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210520 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0005499 abnormal olfactory system morphology IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006018 abnormal tympanic membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12874121 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:12783782 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006211 small orbits IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006284 absent hypaxial muscle IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006284 absent hypaxial muscle IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006285 absent inner ear IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006286 inner ear hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006288 small otic capsule IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:19389353 1550080 Six1 sine oculis-related homeobox 1 gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0008064 decreased otic epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0008065 short endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:16916509 1550080 Six1 sine oculis-related homeobox 1 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:14628042 1550080 Six1 sine oculis-related homeobox 1 gene MP:0008429 absent parotid gland IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0008430 short temporal bone squamous part IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20141003 MGI PMID:16916509 1550080 Six1 sine oculis-related homeobox 1 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22945933 1550080 Six1 sine oculis-related homeobox 1 gene MP:0009520 decreased submandibular gland size IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0009520 decreased submandibular gland size IAGP N RGD:5509061 20150806 MGI PMID:19371398 1550080 Six1 sine oculis-related homeobox 1 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20141003 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0009913 abnormal hyoid bone greater horn morphology IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0010466 vascular ring IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210520 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15955062 1550080 Six1 sine oculis-related homeobox 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550080 Six1 sine oculis-related homeobox 1 gene MP:0011366 absent metanephros IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0011883 absent diaphragm IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12874121 1550080 Six1 sine oculis-related homeobox 1 gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0012754 abnormal cranial neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0013127 epistaxis IAGP N RGD:5509061 20160407 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0013300 abnormal submandibular gland physiology IAGP N RGD:5509061 20150806 MGI PMID:19371398 1550080 Six1 sine oculis-related homeobox 1 gene MP:0013331 abnormal lacrimal gland development IAGP N RGD:5509061 20141204 MGI PMID:12834866 1550080 Six1 sine oculis-related homeobox 1 gene MP:0013541 abnormal submandibular gland development IAGP N RGD:5509061 20150806 MGI PMID:19371398 1550080 Six1 sine oculis-related homeobox 1 gene MP:0013595 absent vomeronasal organ IAGP N RGD:5509061 20150319 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0013929 absent eye muscles IAGP N RGD:5509061 20171026 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0013964 absent tongue muscles IAGP N RGD:5509061 20171026 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0014155 absent olfactory epithelium IAGP N RGD:5509061 20160407 MGI PMID:14695375 1550080 Six1 sine oculis-related homeobox 1 gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20171109 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0030208 abnormal intrinsic tongue muscle morphology IAGP N RGD:5509061 20171026 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0030210 abnormal genioglossus muscle morphology IAGP N RGD:5509061 20171019 MGI PMID:12668636 1550080 Six1 sine oculis-related homeobox 1 gene MP:0030210 abnormal genioglossus muscle morphology IAGP N RGD:5509061 20171026 MGI PMID:15788460 1550080 Six1 sine oculis-related homeobox 1 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20171109 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0030421 tongue muscle hypoplasia IAGP N RGD:5509061 20171214 MGI PMID:21364285 1550080 Six1 sine oculis-related homeobox 1 gene MP:0030426 facial muscle hypoplasia IAGP N RGD:5509061 20171214 MGI PMID:21364285 1550081 Mx2 MX dynamin-like GTPase 2 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200514 MGI 1550081 Mx2 MX dynamin-like GTPase 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20201022 MGI 1550081 Mx2 MX dynamin-like GTPase 2 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20211021 MGI 1550081 Mx2 MX dynamin-like GTPase 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20200514 MGI 1550082 Clcf1 cardiotrophin-like cytokine factor 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20181227 MGI 1550082 Clcf1 cardiotrophin-like cytokine factor 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1550082 Clcf1 cardiotrophin-like cytokine factor 1 gene MP:0000909 abnormal facial motor nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19098279 1550082 Clcf1 cardiotrophin-like cytokine factor 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19098279 1550082 Clcf1 cardiotrophin-like cytokine factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19098279 1550082 Clcf1 cardiotrophin-like cytokine factor 1 gene MP:0001435 absent suckling reflex IAGP N RGD:5509061 20141003 MGI PMID:19098279 1550082 Clcf1 cardiotrophin-like cytokine factor 1 gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20220519 MGI 1550082 Clcf1 cardiotrophin-like cytokine factor 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:19098279 1550082 Clcf1 cardiotrophin-like cytokine factor 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 1550082 Clcf1 cardiotrophin-like cytokine factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19098279 1550082 Clcf1 cardiotrophin-like cytokine factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170105 MGI 1550083 Dusp7 dual specificity phosphatase 7 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1550083 Dusp7 dual specificity phosphatase 7 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1550083 Dusp7 dual specificity phosphatase 7 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1550083 Dusp7 dual specificity phosphatase 7 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1550083 Dusp7 dual specificity phosphatase 7 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20170105 MGI 1550083 Dusp7 dual specificity phosphatase 7 gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20211021 MGI 1550083 Dusp7 dual specificity phosphatase 7 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1550083 Dusp7 dual specificity phosphatase 7 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20211021 MGI 1550083 Dusp7 dual specificity phosphatase 7 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230420 MGI PMID:35596107 1550084 Gpr3 G-protein coupled receptor 3 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15956199 1550084 Gpr3 G-protein coupled receptor 3 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15956199 1550084 Gpr3 G-protein coupled receptor 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15956199 1550084 Gpr3 G-protein coupled receptor 3 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:15956199 1550084 Gpr3 G-protein coupled receptor 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15956199 1550084 Gpr3 G-protein coupled receptor 3 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 1550084 Gpr3 G-protein coupled receptor 3 gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:15956199 1550084 Gpr3 G-protein coupled receptor 3 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:15956199 1550084 Gpr3 G-protein coupled receptor 3 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:15956199 1550084 Gpr3 G-protein coupled receptor 3 gene MP:0009007 short estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:15956199 1550089 Mrm3 mitochondrial rRNA methyltransferase 3 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20200310 MGI 1550089 Mrm3 mitochondrial rRNA methyltransferase 3 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20221215 MGI 1550089 Mrm3 mitochondrial rRNA methyltransferase 3 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20200310 MGI 1550089 Mrm3 mitochondrial rRNA methyltransferase 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1550089 Mrm3 mitochondrial rRNA methyltransferase 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1550089 Mrm3 mitochondrial rRNA methyltransferase 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550089 Mrm3 mitochondrial rRNA methyltransferase 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20200310 MGI 1550089 Mrm3 mitochondrial rRNA methyltransferase 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1550089 Mrm3 mitochondrial rRNA methyltransferase 3 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240620 MGI 1550090 Rprd1b regulation of nuclear pre-mRNA domain containing 1B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20211202 MGI PMID:33431892 1550090 Rprd1b regulation of nuclear pre-mRNA domain containing 1B gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20211202 MGI PMID:33431892 1550090 Rprd1b regulation of nuclear pre-mRNA domain containing 1B gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20211202 MGI PMID:33431892 1550090 Rprd1b regulation of nuclear pre-mRNA domain containing 1B gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20211202 MGI PMID:33431892 1550090 Rprd1b regulation of nuclear pre-mRNA domain containing 1B gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 1550090 Rprd1b regulation of nuclear pre-mRNA domain containing 1B gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20211202 MGI PMID:33431892 1550090 Rprd1b regulation of nuclear pre-mRNA domain containing 1B gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20211202 MGI PMID:33431892 1550090 Rprd1b regulation of nuclear pre-mRNA domain containing 1B gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20211202 MGI PMID:33431892 1550090 Rprd1b regulation of nuclear pre-mRNA domain containing 1B gene MP:0013792 abnormal small intestine goblet cell morphology IAGP N RGD:5509061 20211202 MGI PMID:33431892 1550090 Rprd1b regulation of nuclear pre-mRNA domain containing 1B gene MP:0013793 abnormal large intestine goblet cell morphology IAGP N RGD:5509061 20211202 MGI PMID:33431892 1550090 Rprd1b regulation of nuclear pre-mRNA domain containing 1B gene MP:0031319 impaired intestine regeneration IAGP N RGD:5509061 20211202 MGI PMID:33431892 1550091 Tfb1m transcription factor B1, mitochondrial gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19356719 1550091 Tfb1m transcription factor B1, mitochondrial gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:19356719 1550091 Tfb1m transcription factor B1, mitochondrial gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19356719 1550091 Tfb1m transcription factor B1, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19356719 1550091 Tfb1m transcription factor B1, mitochondrial gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19356719 1550091 Tfb1m transcription factor B1, mitochondrial gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:19356719 1550091 Tfb1m transcription factor B1, mitochondrial gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:19356719 1550091 Tfb1m transcription factor B1, mitochondrial gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19356719 1550091 Tfb1m transcription factor B1, mitochondrial gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:19356719 1550091 Tfb1m transcription factor B1, mitochondrial gene MP:0011389 absent optic disk IAGP N RGD:5509061 20141003 MGI PMID:19356719 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210520 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20200310 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:29718959 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0002833 increased heart weight IEA N RGD:5509061 20200310 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20210128 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200310 MGI PMID:29718959 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:29718959 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:29718959 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20240523 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20200310 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20200310 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20200310 MGI PMID:29718959 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:29718959 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:29718959 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20200310 MGI PMID:29718959 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20200310 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20230601 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0013510 decreased CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0013513 decreased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0013514 increased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 1550092 Gimap6 GTPase, IMAP family member 6 gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20200310 MGI PMID:29718959 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0001177 atelectasis IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0001890 anencephaly IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0012531 delayed limb development IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0013395 eyelid hypoplasia IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550093 Gcn1 GCN1 activator of EIF2AK4 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20201022 MGI PMID:32324833 1550095 Kcnk6 potassium inwardly-rectifying channel, subfamily K, member 6 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:21876070 1550095 Kcnk6 potassium inwardly-rectifying channel, subfamily K, member 6 gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:21876070 1550095 Kcnk6 potassium inwardly-rectifying channel, subfamily K, member 6 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21876070 1550095 Kcnk6 potassium inwardly-rectifying channel, subfamily K, member 6 gene MP:0004878 increased systemic vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:21876070 1550095 Kcnk6 potassium inwardly-rectifying channel, subfamily K, member 6 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21876070 1550095 Kcnk6 potassium inwardly-rectifying channel, subfamily K, member 6 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21876070 1550095 Kcnk6 potassium inwardly-rectifying channel, subfamily K, member 6 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21876070 1550099 Adamts4 ADAM metallopeptidase with thrombospondin type 1 motif 4 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:21584905 1550099 Adamts4 ADAM metallopeptidase with thrombospondin type 1 motif 4 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20018883 1550099 Adamts4 ADAM metallopeptidase with thrombospondin type 1 motif 4 gene MP:0001405 impaired coordination IEA N RGD:5509061 20111116 MGI 1550099 Adamts4 ADAM metallopeptidase with thrombospondin type 1 motif 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15334469 1550099 Adamts4 ADAM metallopeptidase with thrombospondin type 1 motif 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15800625 1550099 Adamts4 ADAM metallopeptidase with thrombospondin type 1 motif 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21584905 1550099 Adamts4 ADAM metallopeptidase with thrombospondin type 1 motif 4 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:20018883 1550099 Adamts4 ADAM metallopeptidase with thrombospondin type 1 motif 4 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20111116 MGI 1550099 Adamts4 ADAM metallopeptidase with thrombospondin type 1 motif 4 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20200514 MGI 1550099 Adamts4 ADAM metallopeptidase with thrombospondin type 1 motif 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20221215 MGI 1550099 Adamts4 ADAM metallopeptidase with thrombospondin type 1 motif 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21584905 1550099 Adamts4 ADAM metallopeptidase with thrombospondin type 1 motif 4 gene MP:0011422 kidney medulla atrophy IAGP N RGD:5509061 20141003 MGI PMID:21584905 1550100 Scrn3 secernin 3 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1550101 Akr1b8 aldo-keto reductase family 1, member B8 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20210617 MGI PMID:25538260 1550101 Akr1b8 aldo-keto reductase family 1, member B8 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20210617 MGI PMID:25538260 1550101 Akr1b8 aldo-keto reductase family 1, member B8 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20210617 MGI PMID:25538260 1550101 Akr1b8 aldo-keto reductase family 1, member B8 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20240523 MGI 1550101 Akr1b8 aldo-keto reductase family 1, member B8 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20240523 MGI 1550101 Akr1b8 aldo-keto reductase family 1, member B8 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20210617 MGI PMID:25538260 1550101 Akr1b8 aldo-keto reductase family 1, member B8 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20210617 MGI PMID:25538260 1550101 Akr1b8 aldo-keto reductase family 1, member B8 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20210617 MGI PMID:25538260 1550101 Akr1b8 aldo-keto reductase family 1, member B8 gene MP:0010052 increased grip strength IEA N RGD:5509061 20160421 MGI 1550101 Akr1b8 aldo-keto reductase family 1, member B8 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20210617 MGI PMID:25538260 1550101 Akr1b8 aldo-keto reductase family 1, member B8 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1550101 Akr1b8 aldo-keto reductase family 1, member B8 gene MP:0020868 decreased lipogenesis IAGP N RGD:5509061 20210617 MGI PMID:25538260 1550101 Akr1b8 aldo-keto reductase family 1, member B8 gene MP:0031319 impaired intestine regeneration IAGP N RGD:5509061 20211125 MGI PMID:25538260 1550103 Trafd1 TRAF type zinc finger domain containing 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1550103 Trafd1 TRAF type zinc finger domain containing 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18849341 1550103 Trafd1 TRAF type zinc finger domain containing 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18849341 1550103 Trafd1 TRAF type zinc finger domain containing 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18849341 1550103 Trafd1 TRAF type zinc finger domain containing 1 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:18849341 1550103 Trafd1 TRAF type zinc finger domain containing 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:18849341 1550103 Trafd1 TRAF type zinc finger domain containing 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:18849341 1550103 Trafd1 TRAF type zinc finger domain containing 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18849341 1550103 Trafd1 TRAF type zinc finger domain containing 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1550103 Trafd1 TRAF type zinc finger domain containing 1 gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:18849341 1550104 Cdcp1 CUB domain containing protein 1 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20200310 MGI PMID:23243018 1550104 Cdcp1 CUB domain containing protein 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20200310 MGI PMID:23243018 1550104 Cdcp1 CUB domain containing protein 1 gene MP:0001200 thick skin IAGP N RGD:5509061 20200310 MGI PMID:23243018 1550104 Cdcp1 CUB domain containing protein 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20200310 MGI PMID:23243018 1550104 Cdcp1 CUB domain containing protein 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:23243018 1550104 Cdcp1 CUB domain containing protein 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:23243018 1550104 Cdcp1 CUB domain containing protein 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20200310 MGI PMID:23243018 1550104 Cdcp1 CUB domain containing protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:23243018 1550104 Cdcp1 CUB domain containing protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:23243018 1550104 Cdcp1 CUB domain containing protein 1 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:23243018 1550104 Cdcp1 CUB domain containing protein 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:23243018 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0000420 ruffled hair IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0002989 small kidney IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550106 Yes1 YES proto-oncogene 1, Src family tyrosine kinase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:7958873 1550108 Dedd death effector domain-containing gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17283331 1550108 Dedd death effector domain-containing gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:17283331 1550108 Dedd death effector domain-containing gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17283331 1550108 Dedd death effector domain-containing gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17283331 1550108 Dedd death effector domain-containing gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:17283331 1550108 Dedd death effector domain-containing gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17283331 1550108 Dedd death effector domain-containing gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17283331 1550108 Dedd death effector domain-containing gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:17283331 1550110 Chp2 calcineurin-like EF hand protein 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1550110 Chp2 calcineurin-like EF hand protein 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20160421 MGI 1550110 Chp2 calcineurin-like EF hand protein 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1550111 Dpyd dihydropyrimidine dehydrogenase gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20181227 MGI 1550111 Dpyd dihydropyrimidine dehydrogenase gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1550111 Dpyd dihydropyrimidine dehydrogenase gene MP:0002574 increased vertical activity IEA N RGD:5509061 20181227 MGI 1550111 Dpyd dihydropyrimidine dehydrogenase gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20160811 MGI 1550112 Fyttd1 forty-two-three domain containing 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1550112 Fyttd1 forty-two-three domain containing 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1550112 Fyttd1 forty-two-three domain containing 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1550112 Fyttd1 forty-two-three domain containing 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 1550112 Fyttd1 forty-two-three domain containing 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20200310 MGI PMID:21059868 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20200310 MGI PMID:8625838 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20200310 MGI PMID:16024804 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0000080 abnormal exoccipital bone morphology IAGP N RGD:5509061 20200310 MGI PMID:8625838 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:12183370 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20200310 MGI PMID:12183370 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20200310 MGI PMID:8625838 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20200310 MGI PMID:8625838 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0000480 increased rib number IAGP N RGD:5509061 20200310 MGI PMID:21059868 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210805 MGI 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0000692 small spleen IEA N RGD:5509061 20210805 MGI 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:11520462 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210805 MGI 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0001147 small testis IEA N RGD:5509061 20210805 MGI 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:8625838 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:8625838 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:8625838 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0002861 abnormal tail bud morphology IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:15741318 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:21059868 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:8625838 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0003049 abnormal lumbar vertebrae morphology IEA N RGD:5509061 20220811 MGI 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20200310 MGI PMID:16024804 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004342 scapular bone foramen IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004342 scapular bone foramen IAGP N RGD:5509061 20200310 MGI PMID:21059868 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004446 split exoccipital bone IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:15741318 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:21059868 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:8625838 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:15741318 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:21059868 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:8625838 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:8625838 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:15741318 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:21059868 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:8625838 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20200310 MGI PMID:16024804 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004659 abnormal odontoid process morphology IAGP N RGD:5509061 20200310 MGI PMID:8625838 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004710 small notochord IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004713 split notochord IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:11520462 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20200310 MGI PMID:12183370 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20200310 MGI PMID:16024804 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20200310 MGI PMID:21059868 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20200310 MGI PMID:11520462 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:16024804 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:21059868 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0006305 abnormal optic eminence morphology IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0006338 abnormal second pharyngeal arch morphology IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20200310 MGI PMID:12183370 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20200310 MGI PMID:15741318 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20200310 MGI PMID:8625838 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20200310 MGI PMID:16024804 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20200310 MGI PMID:15741318 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20200310 MGI PMID:8625838 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16024804 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21059868 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12183370 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21059868 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210805 MGI 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0012180 abnormal somatic mesoderm morphology IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0012264 hindbrain hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550113 Pcgf2 polycomb group ring finger 2 gene MP:0030834 acromion hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:11290297 1550115 Pudp pseudouridine 5'-phosphatase gene MP:0001304 cataract IEA N RGD:5509061 20200310 MGI 1550115 Pudp pseudouridine 5'-phosphatase gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1550115 Pudp pseudouridine 5'-phosphatase gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220811 MGI 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20231207 MGI 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0012066 decreased astrocyte number IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0020389 increased radial glial cell number IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550116 Gatad2b GATA zinc finger domain containing 2B gene MP:0030189 broad snout IAGP N RGD:5509061 20240222 MGI PMID:38238293 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210128 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210826 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210826 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:31661432 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:31661432 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:31661432 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:31661432 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210128 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20220519 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210826 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20220811 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:31661432 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210826 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200310 MGI PMID:31661432 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210826 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200310 MGI PMID:31661432 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:31661432 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20200310 MGI PMID:31661432 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0008988 abnormal liver perisinusoidal space morphology IAGP N RGD:5509061 20200310 MGI PMID:31661432 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20200310 MGI PMID:31661432 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:31661432 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210826 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0011009 increased circulating glutamate dehydrogenase level IAGP N RGD:5509061 20200310 MGI PMID:31661432 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1550118 Mfsd1 major facilitator superfamily domain containing 1 gene MP:0031148 abnormal liver sinusoidal endothelial cell morphology IAGP N RGD:5509061 20201015 MGI PMID:31661432 1550121 Hbb-y hemoglobin Y, beta-like embryonic chain gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17077320 1550122 Churc1 churchill domain containing 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1550122 Churc1 churchill domain containing 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1550122 Churc1 churchill domain containing 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1550122 Churc1 churchill domain containing 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210520 MGI 1550122 Churc1 churchill domain containing 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210520 MGI 1550122 Churc1 churchill domain containing 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1550122 Churc1 churchill domain containing 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1550122 Churc1 churchill domain containing 1 gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20211021 MGI 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16177061 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23624557 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:16177061 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:16177061 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:16177061 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18378794 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10934232 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16177061 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:10934232 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16177061 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16177061 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:10934232 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:16670336 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20656922 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:10934232 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:16177061 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16177061 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16043658 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:16565390 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23624557 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10934232 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20656922 1550123 Ltb4r1 leukotriene B4 receptor 1 gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:10934232 1550130 Erg ETS transcription factor gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18500345 1550130 Erg ETS transcription factor gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:22932696 1550130 Erg ETS transcription factor gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:22932696 1550130 Erg ETS transcription factor gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20160623 MGI PMID:25062690 1550130 Erg ETS transcription factor gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1550130 Erg ETS transcription factor gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20160623 MGI PMID:25062690 1550130 Erg ETS transcription factor gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20190502 MGI 1550130 Erg ETS transcription factor gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18500345 1550130 Erg ETS transcription factor gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22932696 1550130 Erg ETS transcription factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22932696 1550130 Erg ETS transcription factor gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22932696 1550130 Erg ETS transcription factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22932696 1550130 Erg ETS transcription factor gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20160623 MGI PMID:25062690 1550130 Erg ETS transcription factor gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20190502 MGI 1550130 Erg ETS transcription factor gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18500345 1550130 Erg ETS transcription factor gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20160623 MGI PMID:25062690 1550130 Erg ETS transcription factor gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20171012 MGI PMID:26097038 1550130 Erg ETS transcription factor gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20171012 MGI PMID:26097038 1550130 Erg ETS transcription factor gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20160623 MGI PMID:25062690 1550130 Erg ETS transcription factor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18500345 1550130 Erg ETS transcription factor gene MP:0004125 abnormal venule morphology IAGP N RGD:5509061 20160623 MGI PMID:25062690 1550130 Erg ETS transcription factor gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:18500345 1550130 Erg ETS transcription factor gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18500345 1550130 Erg ETS transcription factor gene MP:0005152 pancytopenia IAGP N RGD:5509061 20160623 MGI PMID:25062690 1550130 Erg ETS transcription factor gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:22932696 1550130 Erg ETS transcription factor gene MP:0006137 venoocclusion IAGP N RGD:5509061 20160623 MGI PMID:25062690 1550130 Erg ETS transcription factor gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20171012 MGI PMID:26097038 1550130 Erg ETS transcription factor gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18500345 1550130 Erg ETS transcription factor gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22932696 1550130 Erg ETS transcription factor gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23512661 1550130 Erg ETS transcription factor gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:22932696 1550130 Erg ETS transcription factor gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20201022 MGI 1550130 Erg ETS transcription factor gene MP:0010758 increased right ventricle systolic pressure IAGP N RGD:5509061 20160623 MGI PMID:25062690 1550130 Erg ETS transcription factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18500345 1550130 Erg ETS transcription factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22932696 1550130 Erg ETS transcription factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20171012 MGI PMID:26097038 1550130 Erg ETS transcription factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550130 Erg ETS transcription factor gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20160623 MGI PMID:25062690 1550130 Erg ETS transcription factor gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20220811 MGI 1550130 Erg ETS transcription factor gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1550130 Erg ETS transcription factor gene MP:0020161 increased vascular endothelial cell proliferation IAGP N RGD:5509061 20160623 MGI PMID:25062690 1550133 Atp6ap1 ATPase, H+ transporting, lysosomal accessory protein 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20151112 MGI PMID:22087256 1550133 Atp6ap1 ATPase, H+ transporting, lysosomal accessory protein 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20151112 MGI PMID:22087256 1550133 Atp6ap1 ATPase, H+ transporting, lysosomal accessory protein 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20151112 MGI PMID:22087256 1550133 Atp6ap1 ATPase, H+ transporting, lysosomal accessory protein 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20151112 MGI PMID:22087256 1550133 Atp6ap1 ATPase, H+ transporting, lysosomal accessory protein 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11989824 1550133 Atp6ap1 ATPase, H+ transporting, lysosomal accessory protein 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20151112 MGI PMID:22087256 1550135 Gjb2 gap junction protein, beta 2 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20150226 MGI PMID:24590285 1550135 Gjb2 gap junction protein, beta 2 gene MP:0000032 cochlear degeneration IAGP N RGD:5509061 20141003 MGI PMID:12121617 1550135 Gjb2 gap junction protein, beta 2 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:12121617 1550135 Gjb2 gap junction protein, beta 2 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:24333301 1550135 Gjb2 gap junction protein, beta 2 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:21807945 1550135 Gjb2 gap junction protein, beta 2 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9508777 1550135 Gjb2 gap junction protein, beta 2 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:9508777 1550135 Gjb2 gap junction protein, beta 2 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21807945 1550135 Gjb2 gap junction protein, beta 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:24333301 1550135 Gjb2 gap junction protein, beta 2 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21807945 1550135 Gjb2 gap junction protein, beta 2 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:24333301 1550135 Gjb2 gap junction protein, beta 2 gene MP:0003390 lymphedema IAGP N RGD:5509061 20141003 MGI PMID:21807945 1550135 Gjb2 gap junction protein, beta 2 gene MP:0003878 abnormal ear physiology IAGP N RGD:5509061 20150226 MGI PMID:24590285 1550135 Gjb2 gap junction protein, beta 2 gene MP:0003879 abnormal hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19047635 1550135 Gjb2 gap junction protein, beta 2 gene MP:0003950 abnormal plasma membrane morphology IAGP N RGD:5509061 20150226 MGI PMID:24590285 1550135 Gjb2 gap junction protein, beta 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14686892 1550135 Gjb2 gap junction protein, beta 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:14686892 1550135 Gjb2 gap junction protein, beta 2 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14686892 1550135 Gjb2 gap junction protein, beta 2 gene MP:0004265 abnormal placental transport IAGP N RGD:5509061 20141003 MGI PMID:9508777 1550135 Gjb2 gap junction protein, beta 2 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:24333301 1550135 Gjb2 gap junction protein, beta 2 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12121617 1550135 Gjb2 gap junction protein, beta 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12121617 1550135 Gjb2 gap junction protein, beta 2 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:12121617 1550135 Gjb2 gap junction protein, beta 2 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:12121617 1550135 Gjb2 gap junction protein, beta 2 gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:24333301 1550135 Gjb2 gap junction protein, beta 2 gene MP:0004482 abnormal interdental cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12121617 1550135 Gjb2 gap junction protein, beta 2 gene MP:0004562 abnormal inner hair cell synaptic ribbon morphology IAGP N RGD:5509061 20141003 MGI PMID:12121617 1550135 Gjb2 gap junction protein, beta 2 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12121617 1550135 Gjb2 gap junction protein, beta 2 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20150226 MGI PMID:24590285 1550135 Gjb2 gap junction protein, beta 2 gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:21807945 1550135 Gjb2 gap junction protein, beta 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0006403 abnormal cochlear endolymph ionic homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12121617 1550135 Gjb2 gap junction protein, beta 2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9508777 1550135 Gjb2 gap junction protein, beta 2 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0010194 absent lymphatic vessels IAGP N RGD:5509061 20141003 MGI PMID:21807945 1550135 Gjb2 gap junction protein, beta 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14686892 1550135 Gjb2 gap junction protein, beta 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9508777 1550135 Gjb2 gap junction protein, beta 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21807945 1550135 Gjb2 gap junction protein, beta 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20141003 MGI PMID:9508777 1550135 Gjb2 gap junction protein, beta 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12121617 1550135 Gjb2 gap junction protein, beta 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20926451 1550135 Gjb2 gap junction protein, beta 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20150226 MGI PMID:24590285 1550136 Cdhr1 cadherin-related family member 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11738025 1550136 Cdhr1 cadherin-related family member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19672243 1550136 Cdhr1 cadherin-related family member 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11738025 1550136 Cdhr1 cadherin-related family member 1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:11738025 1550139 Acvr2a activin receptor IIA gene MP:0000111 cleft palate IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0000125 absent incisors IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20201022 MGI 1550139 Acvr2a activin receptor IIA gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0000371 diluted coat color IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0000399 increased curvature of guard hairs IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0000401 increased curvature of awl hairs IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0000405 abnormal auchene hair morphology IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0000414 alopecia IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20200310 MGI 1550139 Acvr2a activin receptor IIA gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20200310 MGI PMID:16991118 1550139 Acvr2a activin receptor IIA gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0001219 thick epidermis IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1550139 Acvr2a activin receptor IIA gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1550139 Acvr2a activin receptor IIA gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200310 MGI 1550139 Acvr2a activin receptor IIA gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20200310 MGI PMID:16991118 1550139 Acvr2a activin receptor IIA gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:16991118 1550139 Acvr2a activin receptor IIA gene MP:0001749 suppressed circulating follicle stimulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:16991118 1550139 Acvr2a activin receptor IIA gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20200310 MGI PMID:11416011 1550139 Acvr2a activin receptor IIA gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20221215 MGI 1550139 Acvr2a activin receptor IIA gene MP:0003087 absent allantois IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0003812 abnormal hair medulla IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0003875 abnormal hair follicle regression IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20200310 MGI PMID:16991118 1550139 Acvr2a activin receptor IIA gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:16991118 1550139 Acvr2a activin receptor IIA gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:11416011 1550139 Acvr2a activin receptor IIA gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200310 MGI PMID:11416011 1550139 Acvr2a activin receptor IIA gene MP:0004924 abnormal behavior IEA N RGD:5509061 20221215 MGI 1550139 Acvr2a activin receptor IIA gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20201022 MGI 1550139 Acvr2a activin receptor IIA gene MP:0005030 absent amnion IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0005072 abnormal hair follicle melanin granule morphology IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0005163 cyclopia IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0006206 embryonic lethality between somite formation and embryo turning IAGP N RGD:5509061 20200310 MGI PMID:16991118 1550139 Acvr2a activin receptor IIA gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20200310 MGI PMID:11416011 1550139 Acvr2a activin receptor IIA gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20200310 MGI PMID:11416011 1550139 Acvr2a activin receptor IIA gene MP:0008732 reduced hair shaft melanin granule number IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0008733 abnormal hair shaft melanin granule distribution IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0008767 abnormal hair medullary septa cells IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0008975 delayed male fertility IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0009002 premature hair regrowth IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0009081 thin uterus IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0009351 thin hair shaft IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0009659 striated fur IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0010389 mosaic coat color IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0010684 abnormal hair follicle outer root sheath morphology IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:7885474 1550139 Acvr2a activin receptor IIA gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1550139 Acvr2a activin receptor IIA gene MP:0011191 increased embryonic epiblast cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0012081 absent heart tube IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20200310 MGI PMID:16991118 1550139 Acvr2a activin receptor IIA gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0012401 long nails IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0012724 absent head fold IAGP N RGD:5509061 20200310 MGI PMID:10452853 1550139 Acvr2a activin receptor IIA gene MP:0030574 increased hair follicle cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0030918 small melanosome IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0030919 absent hair follicle bulb IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0030922 absent hair club IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0030924 early exit from telogen phase IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0030925 early exit from anagen phase IAGP N RGD:5509061 20200310 MGI PMID:22611050 1550139 Acvr2a activin receptor IIA gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:7885474 1550140 Parp3 poly (ADP-ribose) polymerase family, member 3 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20200310 MGI PMID:21270334 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:22281501 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:2090433 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0000566 synostosis IAGP N RGD:5509061 20141003 MGI PMID:2090433 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:2090433 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:22281501 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0000745 tremors IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:7894157 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:2090433 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:2090433 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:22281501 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0010653 abnormal Wallerian degeneration IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0012051 spasticity IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0020336 abnormal motor neuron dendrite morphology IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0030191 narrow snout IAGP N RGD:5509061 20171019 MGI PMID:22281501 1550141 Mdga2 MAM domain containing glycosylphosphatidylinositol anchor 2 gene MP:0030835 abnormal ankle joint morphology IAGP N RGD:5509061 20190215 MGI PMID:28040732 1550142 Slc25a25 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21296886 1550142 Slc25a25 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:21296886 1550142 Slc25a25 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21296886 1550142 Slc25a25 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25 gene MP:0003060 increased aerobic running capacity IAGP N RGD:5509061 20141003 MGI PMID:21296886 1550142 Slc25a25 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25 gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20141003 MGI PMID:21296886 1550142 Slc25a25 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:21296886 1550142 Slc25a25 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21296886 1550142 Slc25a25 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21296886 1550142 Slc25a25 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25 gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21296886 1550142 Slc25a25 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21296886 1550142 Slc25a25 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:21296886 1550142 Slc25a25 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21296886 1550142 Slc25a25 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:21296886 1550142 Slc25a25 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21296886 1550142 Slc25a25 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 25 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:21296886 1550144 Meis2 Meis homeobox 2 gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20220922 MGI PMID:32169905 1550144 Meis2 Meis homeobox 2 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20220922 MGI PMID:32169905 1550144 Meis2 Meis homeobox 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0000601 small liver IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0001072 abnormal vestibulocochlear nerve morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0001577 anemia IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20220922 MGI PMID:32169905 1550144 Meis2 Meis homeobox 2 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20220922 MGI PMID:32169905 1550144 Meis2 Meis homeobox 2 gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20221027 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0004383 absent interparietal bone IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20220922 MGI PMID:32169905 1550144 Meis2 Meis homeobox 2 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20220922 MGI PMID:32169905 1550144 Meis2 Meis homeobox 2 gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20220922 MGI PMID:32169905 1550144 Meis2 Meis homeobox 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20220922 MGI PMID:32169905 1550144 Meis2 Meis homeobox 2 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20220922 MGI PMID:32169905 1550144 Meis2 Meis homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20220922 MGI PMID:32169905 1550144 Meis2 Meis homeobox 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0011615 submucous cleft palate IAGP N RGD:5509061 20220922 MGI PMID:32169905 1550144 Meis2 Meis homeobox 2 gene MP:0012250 absent heart valves IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0012747 abnormal cardiac neural crest cell morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0013183 absent trigeminal ganglion IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20171109 MGI PMID:26545946 1550144 Meis2 Meis homeobox 2 gene MP:0013546 cleft soft palate IAGP N RGD:5509061 20220922 MGI PMID:32169905 1550144 Meis2 Meis homeobox 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:32169905 1550144 Meis2 Meis homeobox 2 gene MP:0031458 absent palate bones IAGP N RGD:5509061 20221124 MGI PMID:32169905 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:22186026 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20150723 MGI PMID:21882344 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20151217 MGI PMID:24452334 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20150723 MGI PMID:21882344 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20150723 MGI PMID:21882344 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:22186026 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22186026 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20151217 MGI PMID:24452334 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:22186026 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20150723 MGI PMID:21882344 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20151126 MGI PMID:25059425 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20150723 MGI PMID:21882344 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20150723 MGI PMID:21882344 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0002715 decreased glycogen catabolism rate IAGP N RGD:5509061 20141003 MGI PMID:21077101 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20150723 MGI PMID:21882344 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20150723 MGI PMID:21882344 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20150723 MGI PMID:21882344 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20150723 MGI PMID:21882344 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20151217 MGI PMID:24452334 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20150723 MGI PMID:21882344 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22186026 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0005440 increased glycogen level IAGP N RGD:5509061 20141003 MGI PMID:20538597 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:22186026 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20151217 MGI PMID:24452334 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:22186026 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20141003 MGI PMID:22186026 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:21077101 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:20538597 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:21077101 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20150723 MGI PMID:21882344 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0014063 Lafora bodies IAGP N RGD:5509061 20160304 MGI PMID:20538597 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0014063 Lafora bodies IAGP N RGD:5509061 20160304 MGI PMID:21077101 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0014063 Lafora bodies IAGP N RGD:5509061 20160304 MGI PMID:21882344 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0014063 Lafora bodies IAGP N RGD:5509061 20160304 MGI PMID:22186026 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20160310 MGI PMID:20538597 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0014074 increased brain glycogen level IAGP N RGD:5509061 20160310 MGI PMID:20538597 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0014074 increased brain glycogen level IAGP N RGD:5509061 20190711 MGI PMID:24452334 1550145 Nhlrc1 NHL repeat containing 1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:24452334 1550147 Prokr2 prokineticin receptor 2 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220407 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17202262 1550147 Prokr2 prokineticin receptor 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17202262 1550147 Prokr2 prokineticin receptor 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0004894 uterus atrophy IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0004895 vagina atrophy IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:17202262 1550147 Prokr2 prokineticin receptor 2 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17202262 1550147 Prokr2 prokineticin receptor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17202262 1550147 Prokr2 prokineticin receptor 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16537498 1550147 Prokr2 prokineticin receptor 2 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:17202262 1550147 Prokr2 prokineticin receptor 2 gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:17202262 1550148 Nt5dc1 5'-nucleotidase domain containing 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20200310 MGI 1550148 Nt5dc1 5'-nucleotidase domain containing 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1550148 Nt5dc1 5'-nucleotidase domain containing 1 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20211021 MGI 1550148 Nt5dc1 5'-nucleotidase domain containing 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1550148 Nt5dc1 5'-nucleotidase domain containing 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1550148 Nt5dc1 5'-nucleotidase domain containing 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000160 kyphosis IAGP N RGD:5509061 20210722 MGI PMID:11005611 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:6682087 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10369263 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4588955 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000397 abnormal guard hair morphology IAGP N RGD:5509061 20141003 MGI PMID:10369263 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000405 abnormal auchene hair morphology IAGP N RGD:5509061 20141003 MGI PMID:10369263 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:14567972 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:4588955 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:6682087 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:10369263 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000418 focal hair loss IEA N RGD:5509061 20111116 MGI 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:6682087 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:6682087 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:6682087 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000674 abnormal sweat gland morphology IAGP N RGD:5509061 20210722 MGI PMID:11005611 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000852 small cerebellum IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:14567972 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:10369263 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:14567972 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:6682087 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:4588955 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:4588955 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001265 decreased body size IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:6682087 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20210722 MGI PMID:11005611 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001326 retina degeneration IAGP N RGD:5509061 20210722 MGI PMID:11005611 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:4588955 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001393 ataxia IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:4588955 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:6682087 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:14567972 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0002083 premature death IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:6682087 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:6682087 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:6682087 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:4588955 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0002772 brachypodia IAGP N RGD:5509061 20230824 MGI PMID:4588955 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:10369263 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0003417 premature endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:6682087 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:6682087 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0004703 abnormal vertebral column morphology IEA N RGD:5509061 20111116 MGI 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0004704 short vertebral column IEA N RGD:5509061 20111116 MGI 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10369263 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0006253 clinodactyly IAGP N RGD:5509061 20141003 MGI PMID:4588955 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0008283 small hippocampus IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0010387 abnormal Bergmann glial cell morphology IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10369263 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14567972 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:4588955 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10369263 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0011527 disorganized placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:15639195 1550149 Nsdhl NAD(P) dependent steroid dehydrogenase-like gene MP:0012204 abnormal neuronal stem cell physiology IAGP N RGD:5509061 20170518 MGI PMID:25652406 1550152 Il12rb1 interleukin 12 receptor, beta 1 gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18504307 1550152 Il12rb1 interleukin 12 receptor, beta 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1550152 Il12rb1 interleukin 12 receptor, beta 1 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:9257825 1550152 Il12rb1 interleukin 12 receptor, beta 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9257825 1550152 Il12rb1 interleukin 12 receptor, beta 1 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:9257825 1550152 Il12rb1 interleukin 12 receptor, beta 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1550152 Il12rb1 interleukin 12 receptor, beta 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20191128 MGI 1550152 Il12rb1 interleukin 12 receptor, beta 1 gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20240523 MGI 1550153 Cyth3 cytohesin 3 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20191024 MGI PMID:30837656 1550153 Cyth3 cytohesin 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20191024 MGI PMID:30837656 1550153 Cyth3 cytohesin 3 gene MP:0003213 decreased susceptibility to age related obesity IAGP N RGD:5509061 20191024 MGI PMID:30837656 1550153 Cyth3 cytohesin 3 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20191024 MGI PMID:30837656 1550153 Cyth3 cytohesin 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20191024 MGI PMID:30837656 1550153 Cyth3 cytohesin 3 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20191024 MGI PMID:30837656 1550153 Cyth3 cytohesin 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20191024 MGI PMID:30837656 1550153 Cyth3 cytohesin 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20191024 MGI PMID:30837656 1550153 Cyth3 cytohesin 3 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20191024 MGI PMID:30837656 1550153 Cyth3 cytohesin 3 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20191024 MGI PMID:30837656 1550153 Cyth3 cytohesin 3 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20191024 MGI PMID:30837656 1550153 Cyth3 cytohesin 3 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20191024 MGI PMID:30837656 1550153 Cyth3 cytohesin 3 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20191024 MGI PMID:30837656 1550153 Cyth3 cytohesin 3 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191024 MGI PMID:30837656 1550153 Cyth3 cytohesin 3 gene MP:0014476 abnormal feces lipid level IAGP N RGD:5509061 20240704 MGI PMID:30837656 1550153 Cyth3 cytohesin 3 gene MP:0020868 decreased lipogenesis IAGP N RGD:5509061 20191024 MGI PMID:30837656 1550154 Rnf152 ring finger protein 152 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20240516 MGI PMID:30514904 1550156 Ik IK cytokine gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20240523 MGI 1550156 Ik IK cytokine gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1550156 Ik IK cytokine gene MP:0003960 increased lean body mass IEA N RGD:5509061 20231207 MGI 1550156 Ik IK cytokine gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1550156 Ik IK cytokine gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1550156 Ik IK cytokine gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1550156 Ik IK cytokine gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230601 MGI 1550156 Ik IK cytokine gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20230601 MGI 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000023 abnormal ear position IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:14699048 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:20233966 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:28846072 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:30423293 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20210225 MGI PMID:30952657 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:17476360 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:14699048 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:28846072 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20200310 MGI PMID:15864294 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000231 hypertension IAGP N RGD:5509061 20200310 MGI PMID:15864294 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20200310 MGI PMID:14699048 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20200310 MGI PMID:16720837 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200310 MGI PMID:9294608 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000274 enlarged heart IAGP N RGD:5509061 20200310 MGI PMID:15093544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000275 heart hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20200310 MGI PMID:9294608 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000292 distended pericardium IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:12957286 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:20609353 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:22892241 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:23266956 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:17476360 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:20609353 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21514245 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20200310 MGI PMID:17476360 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000420 ruffled hair IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000441 increased cranium width IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000447 flattened snout IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20200310 MGI PMID:21965329 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:18372904 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20200310 MGI PMID:15093544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20210225 MGI PMID:30952657 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000592 short tail IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:17476360 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000599 enlarged liver IAGP N RGD:5509061 20200310 MGI PMID:14699048 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000599 enlarged liver IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000601 small liver IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000603 pale liver IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000610 cholestasis IAGP N RGD:5509061 20200310 MGI PMID:15894267 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000611 jaundice IAGP N RGD:5509061 20200310 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000611 jaundice IAGP N RGD:5509061 20200310 MGI PMID:22113502 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000611 jaundice IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:19117991 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:21965329 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20200310 MGI PMID:17476360 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:14699048 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:16720837 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20210225 MGI PMID:30952657 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000753 paralysis IAGP N RGD:5509061 20200310 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200310 MGI PMID:18371380 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000858 abnormal metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:17936562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20200310 MGI PMID:15093544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20200310 MGI PMID:18371380 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18371380 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20200310 MGI PMID:15619626 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20200310 MGI PMID:22350410 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:18281487 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20200310 MGI PMID:17468755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20200310 MGI PMID:19151761 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20200310 MGI PMID:20141835 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20200310 MGI PMID:20697345 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20200310 MGI PMID:25252692 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001212 skin lesions IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001219 thick epidermis IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001260 increased body weight IAGP N RGD:5509061 20241031 MGI PMID:38574733 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:17476360 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:18281487 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:22113502 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:22964582 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:28846072 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001270 distended abdomen IAGP N RGD:5509061 20200310 MGI PMID:15894267 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001270 distended abdomen IAGP N RGD:5509061 20200310 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001270 distended abdomen IAGP N RGD:5509061 20200310 MGI PMID:20807812 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001270 distended abdomen IAGP N RGD:5509061 20200310 MGI PMID:22113502 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001270 distended abdomen IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:14681207 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:15619626 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:16288016 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:16585505 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:17349585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:17486075 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:17607363 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:17676035 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:17676052 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:18713982 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:19351816 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:21911454 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:22266220 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:22350410 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:23999427 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:25180607 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:28790031 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:18713982 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:25180607 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:28294115 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20240905 MGI PMID:38733589 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20200310 MGI PMID:22745308 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:22964582 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:14699048 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:16720837 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:20233966 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:28846072 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001577 anemia IAGP N RGD:5509061 20210225 MGI PMID:30952657 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20200310 MGI PMID:14699048 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20200310 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:15093544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:9294608 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:17476360 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:20807812 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001787 pericardial edema IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:16288213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:18281487 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:22964582 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20200310 MGI PMID:19629168 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:20179099 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20230302 MGI PMID:32552404 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20200310 MGI PMID:19629168 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20200310 MGI PMID:23453624 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001953 respiratory failure IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:12957286 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:17476360 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:21458673 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:22964582 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:12957286 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:15894267 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:17486075 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:23999427 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:14681207 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17468755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:11323676 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:14706336 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17114584 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17486075 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:20141835 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:20609353 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21458673 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:24239359 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:24591640 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:11323676 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:15894267 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17936562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20832755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:27462406 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20200310 MGI PMID:28846072 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:11323676 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:12957286 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:15837621 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:16288016 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:16288213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17468755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17476360 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17676035 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17936562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18281487 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18493606 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19151761 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19847165 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21317887 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21911454 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22228755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22430205 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22611036 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22964582 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:23285300 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:23565506 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:24430184 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20240829 MGI PMID:36548081 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19846776 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:12957286 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17486075 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17676052 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19956606 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21512139 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22228755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:24239359 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17486075 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17607363 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20080688 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21965329 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:12957286 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20080688 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20210225 MGI PMID:30952657 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:11323676 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:12957286 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:15837621 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:16288016 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17468755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17476360 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17486075 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17936562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18281487 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19061836 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20308544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20832755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21458673 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21911454 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22411819 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22606359 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22892241 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:23285300 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:24239348 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:24430184 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:2891865 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:8152802 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20240829 MGI PMID:36548081 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:11323676 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:17607363 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:17936562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:21504907 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:22699621 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:27462406 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:20609353 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:20832755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:27462406 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20220428 MGI PMID:31400748 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20241031 MGI PMID:38574733 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20200310 MGI PMID:17540175 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20200310 MGI PMID:19847165 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20230302 MGI PMID:32552404 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:11323676 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:12957286 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:14699048 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:15619626 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:15894267 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:16023597 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:16288016 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:16288213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:17349585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:17468755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:17486075 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:17676035 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:17936562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:18281487 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:18372904 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:18621715 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19117991 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19151761 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19351816 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19846776 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:20233966 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:20308544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:20609353 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:20697345 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:20807812 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:20832755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21056012 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21317887 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21368895 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21458673 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21504907 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21514245 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21911454 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21965329 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:22113502 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:22266220 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:22350410 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:22411819 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:22699621 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:22932805 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:24430184 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:27462406 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:28790031 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:28846072 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:28934293 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:30423293 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:31685994 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200423 MGI PMID:30858608 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20210225 MGI PMID:30952657 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002083 premature death IAGP N RGD:5509061 20241024 MGI PMID:31048544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:17476360 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002138 abnormal hepatobiliary system morphology IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:14645534 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15864294 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:18059342 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:9294608 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:18371380 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002188 small heart IAGP N RGD:5509061 20200310 MGI PMID:9294608 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20200310 MGI PMID:18493606 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20200310 MGI PMID:18493606 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20200310 MGI PMID:19151761 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20200310 MGI PMID:22411819 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20210225 MGI PMID:30952657 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20200310 MGI PMID:20233966 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002493 increased IgG level IAGP N RGD:5509061 20200310 MGI PMID:19841240 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:19841240 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002606 increased basophil cell number IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20200310 MGI PMID:16720837 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20200310 MGI PMID:16720837 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200310 MGI PMID:9294608 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002732 increased trichoepithelioma incidence IAGP N RGD:5509061 20200310 MGI PMID:23999427 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:15864294 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20210225 MGI PMID:30952657 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:20697345 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18372904 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:20308544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200310 MGI PMID:15864294 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200310 MGI PMID:28846072 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:9294608 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20200310 MGI PMID:29386660 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20200310 MGI PMID:15894267 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20200310 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003277 increased esophageal papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003277 increased esophageal papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:15894267 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20643348 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003335 exocrine pancreatic insufficiency IAGP N RGD:5509061 20200310 MGI PMID:21056012 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20200310 MGI PMID:17114584 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20200310 MGI PMID:19629168 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20200310 MGI PMID:23266956 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003357 impaired granulosa cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003390 lymphedema IAGP N RGD:5509061 20200310 MGI PMID:20179099 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:19151761 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:19847165 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:20308544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:20609353 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:20832755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:23063435 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:26095252 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:27462406 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:31685994 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20200310 MGI PMID:17486075 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20200310 MGI PMID:17607363 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20200310 MGI PMID:19151761 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20200310 MGI PMID:19847165 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18372904 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20200310 MGI PMID:14706336 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:9294608 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20200310 MGI PMID:21965329 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20200310 MGI PMID:28846072 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:11323676 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:12957286 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17486075 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:26095252 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003717 pallor IAGP N RGD:5509061 20200310 MGI PMID:15093544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003717 pallor IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003717 pallor IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:19151761 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:20697345 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:20832755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:22228755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:22430205 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003750 increased mouth tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:24525739 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003752 increased oral papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003752 increased oral papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:22699621 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003752 increased oral papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:24525739 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003780 increased lip tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17936562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20200310 MGI PMID:23266956 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:9294608 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:21576358 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:21576358 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20200310 MGI PMID:16023597 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004155 decreased susceptibility to induced pancreatitis IAGP N RGD:5509061 20241031 MGI PMID:38574733 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17486075 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17607363 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004247 small pancreas IAGP N RGD:5509061 20241031 MGI PMID:38574733 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:15093544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004390 abnormal bronchoalveolar duct junction morphology IAGP N RGD:5509061 20200310 MGI PMID:22411819 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20200310 MGI PMID:17607363 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20200310 MGI PMID:17607363 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20200310 MGI PMID:15864294 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20241024 MGI PMID:31048544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20200310 MGI PMID:28846072 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:29386660 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:11323676 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:18372904 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20210225 MGI PMID:30952657 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:15619626 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004882 enlarged lung IAGP N RGD:5509061 20200310 MGI PMID:17468755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004937 dilated heart IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20230302 MGI PMID:32552404 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20200310 MGI PMID:19841240 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200310 MGI PMID:21911454 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005015 increased T cell number IAGP N RGD:5509061 20200310 MGI PMID:21911454 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:17476360 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:28846072 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:28846072 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005084 abnormal gallbladder morphology IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20200310 MGI PMID:28846072 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:28846072 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20200310 MGI PMID:16720837 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005119 decreased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:19351816 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005150 cachexia IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005150 cachexia IAGP N RGD:5509061 20200310 MGI PMID:15894267 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005150 cachexia IAGP N RGD:5509061 20200310 MGI PMID:21458673 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20200310 MGI PMID:20807812 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20200310 MGI PMID:19629168 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005324 ascites IAGP N RGD:5509061 20200310 MGI PMID:20807812 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005324 ascites IAGP N RGD:5509061 20200310 MGI PMID:22113502 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20200310 MGI PMID:19351816 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20200310 MGI PMID:23597566 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005426 tachypnea IAGP N RGD:5509061 20200310 MGI PMID:18281487 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20200310 MGI PMID:22266220 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20200310 MGI PMID:19351816 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005488 bronchial epithelial hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20200310 MGI PMID:16720837 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005630 increased lung weight IAGP N RGD:5509061 20200310 MGI PMID:17476360 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0005630 increased lung weight IAGP N RGD:5509061 20200310 MGI PMID:20308544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20230302 MGI PMID:32552404 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20200310 MGI PMID:15864294 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20200310 MGI PMID:15864294 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0006321 increased myocardial fiber number IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:20308544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:25813352 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17936562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:20505730 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20200310 MGI PMID:20609353 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:11323676 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:16288016 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17468755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17476360 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17676035 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17936562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:18264106 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:18281487 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19010921 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19029981 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19061836 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19151761 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:20308544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:20609353 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:20832755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21317887 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21504907 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21512139 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:22964582 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:24276238 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:27462406 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20210211 MGI PMID:32767810 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20240829 MGI PMID:36548081 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008018 increased facial tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20200310 MGI PMID:21317887 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20200310 MGI PMID:28846072 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:21911454 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:26095252 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:19841240 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18281487 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20308544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20609353 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20832755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21514245 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22611036 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22964582 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:23453624 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008717 increased lung squamous cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17676035 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008718 increased lung large cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17676035 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:21514245 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008780 increased pancreatic acinar cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21056012 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20200310 MGI PMID:15894267 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:20852630 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009043 increased pancreas adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22113502 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20200310 MGI PMID:18713982 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009110 pancreas hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:19629168 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009143 abnormal pancreatic duct morphology IAGP N RGD:5509061 20200310 MGI PMID:12957286 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009143 abnormal pancreatic duct morphology IAGP N RGD:5509061 20200310 MGI PMID:25042889 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20200310 MGI PMID:19629168 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20200310 MGI PMID:29670173 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:14681207 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:14706336 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:15894267 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:16585505 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17114584 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17349585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18621715 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18713982 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20807812 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21056012 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22611036 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22699621 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:23453624 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:25042889 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:25878147 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:28790031 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:28934293 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:31685994 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20200423 MGI PMID:30858608 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20210225 MGI PMID:30952657 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20241024 MGI PMID:31048544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20241031 MGI PMID:38574733 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:14681207 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:15894267 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:18713982 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:19028870 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:19028876 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:19629168 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:20473331 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:20807812 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:22113502 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:22699621 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:25042889 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:26996122 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:28790031 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:28934293 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:29670173 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:31685994 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20210225 MGI PMID:30952657 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20241024 MGI PMID:31048544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:14681207 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:16585505 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:18713982 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19629168 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:20807812 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:22113502 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:22699621 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:23453624 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:26996122 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20241024 MGI PMID:31048544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20241031 MGI PMID:38574733 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009164 exocrine pancreas atrophy IAGP N RGD:5509061 20200310 MGI PMID:20807812 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20200310 MGI PMID:14681207 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009216 abnormal peritoneum morphology IAGP N RGD:5509061 20200310 MGI PMID:15619626 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:19117991 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:21965329 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19117991 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21965329 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22350410 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009221 uterus adenomyosis IAGP N RGD:5509061 20200310 MGI PMID:19841240 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20200310 MGI PMID:19629168 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:16288016 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17676052 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20080688 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20609353 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22113502 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22411819 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009320 increased lymphoblastic lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:14699048 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009343 dilated gallbladder IAGP N RGD:5509061 20200310 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009343 dilated gallbladder IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009493 abnormal cystic duct morphology IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009498 abnormal extrahepatic bile duct morphology IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009523 submandibular gland hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:15093544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009535 abnormal skin sebaceous gland morphology IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21368895 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:23999427 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009794 sebaceous gland hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009797 abnormal mismatch repair IAGP N RGD:5509061 20200310 MGI PMID:18264106 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20200310 MGI PMID:17349585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010020 spleen vascular congestion IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17540175 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19029981 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:20832755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:24430184 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:25813352 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:26095252 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:27462406 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:2891865 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:8152802 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20201112 MGI PMID:30686754 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20210211 MGI PMID:32767810 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20240829 MGI PMID:36548081 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:27462406 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010273 increased classified tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19846776 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010274 increased organ/body region tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:20080688 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010274 increased organ/body region tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21565614 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20697345 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010283 decreased classified tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21514245 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010285 decreased skin tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:27462406 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17468755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:23999427 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17114584 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22266220 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20200310 MGI PMID:17936562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20200310 MGI PMID:22034435 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010309 increased mesothelioma incidence IAGP N RGD:5509061 20200310 MGI PMID:17486075 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010314 increased neurofibroma incidence IAGP N RGD:5509061 20200310 MGI PMID:17936562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010314 increased neurofibroma incidence IAGP N RGD:5509061 20200310 MGI PMID:19846776 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17936562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22266220 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:29386660 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20200310 MGI PMID:25252692 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19351816 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010349 increased teratocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:15894267 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19117991 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:11323676 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17486075 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010367 increased spindle cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17607363 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010367 increased spindle cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20697345 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:14699048 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:14966562 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:22932805 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20609353 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:23999427 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010588 conotruncal ridge hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010668 abnormal hepatic portal vein morphology IAGP N RGD:5509061 20200310 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010769 abnormal survival IAGP N RGD:5509061 20200310 MGI PMID:28294115 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010799 stomach mucosa hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20200310 MGI PMID:23285300 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010910 bronchiolar epithelial hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:19151761 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010943 abnormal bronchus epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010945 lung epithelium hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:20308544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010945 lung epithelium hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:20832755 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0010945 lung epithelium hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:24276238 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011032 impaired branching involved in terminal bronchiole morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18059342 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20308544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20807812 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25042889 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17476360 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20230302 MGI PMID:32552404 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18059342 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9294608 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12957286 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15093544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18059342 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12957286 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20200310 MGI PMID:16720837 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011702 abnormal fibroblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:12957286 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:22606359 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:22892241 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20220428 MGI PMID:31400748 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011861 increased cranium height IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0012080 chylous ascites IAGP N RGD:5509061 20200310 MGI PMID:20179099 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200310 MGI PMID:21576358 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200310 MGI PMID:21576358 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0012416 decreased gland tumor incidence IAGP N RGD:5509061 20231102 MGI PMID:36241718 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0012416 decreased gland tumor incidence IAGP N RGD:5509061 20241024 MGI PMID:31048544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17486075 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0012433 decreased ovarian tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:20505730 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0012546 triangular face IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20200310 MGI PMID:15093544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20200310 MGI PMID:15894267 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20200310 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20200310 MGI PMID:25042889 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20200310 MGI PMID:27032374 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013220 increased pancreas apoptosis IAGP N RGD:5509061 20200310 MGI PMID:21056012 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20200310 MGI PMID:20807812 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20200310 MGI PMID:25042889 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20241024 MGI PMID:31048544 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013272 abnormal translation IAGP N RGD:5509061 20200423 MGI PMID:30858608 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013331 abnormal lacrimal gland development IAGP N RGD:5509061 20200310 MGI PMID:22745308 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013415 increased myeloid cell number in bone marrow IAGP N RGD:5509061 20210225 MGI PMID:30952657 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013443 Harderian gland hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:12957286 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:17369402 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:9334313 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20210225 MGI PMID:30952657 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013696 increased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20200310 MGI PMID:25359213 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013733 squamous metaplasia of bulbourethral gland IAGP N RGD:5509061 20200310 MGI PMID:19117991 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013735 squamous metaplasia of urethral gland IAGP N RGD:5509061 20200310 MGI PMID:19117991 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18372904 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0014076 absent Paneth cells IAGP N RGD:5509061 20210225 MGI PMID:30952657 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20240829 MGI PMID:36548081 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:14681207 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:17114584 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:22411819 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:23285300 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20240829 MGI PMID:36548081 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0020190 abnormal lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:25813352 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0030574 increased hair follicle cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21502497 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0030737 decreased glutamic acid level IAGP N RGD:5509061 20200310 MGI PMID:31685994 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20200310 MGI PMID:17607363 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0031058 hepatosplenomegaly IAGP N RGD:5509061 20200618 MGI PMID:28846072 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0031159 abnormal hepatic portal vein thrombosis IAGP N RGD:5509061 20201210 MGI PMID:17114585 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0031440 lymphatic vessel hypoplasia IAGP N RGD:5509061 20220915 MGI PMID:20179099 1550157 Kras Kirsten rat sarcoma viral oncogene homolog gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15864294 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20201022 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0001297 microphthalmia IEA N RGD:5509061 20201022 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20240523 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20210826 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0001399 hyperactivity IEA N RGD:5509061 20221215 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20201022 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20221215 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0002608 increased hematocrit IEA N RGD:5509061 20220519 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0005287 narrow eye opening IEA N RGD:5509061 20201231 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210520 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0009454 impaired contextual conditioning behavior IEA N RGD:5509061 20231207 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20240829 MGI PMID:36943869 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20240829 MGI PMID:36943869 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20240829 MGI PMID:36943869 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20240829 MGI PMID:36943869 1550160 Ubl7 ubiquitin-like 7 (bone marrow stromal cell-derived) gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20240829 MGI PMID:36943869 1550161 Mxra8 matrix-remodelling associated 8 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1550161 Mxra8 matrix-remodelling associated 8 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1550161 Mxra8 matrix-remodelling associated 8 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20191212 MGI PMID:31484075 1550161 Mxra8 matrix-remodelling associated 8 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1550161 Mxra8 matrix-remodelling associated 8 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1550161 Mxra8 matrix-remodelling associated 8 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20191212 MGI PMID:31484075 1550161 Mxra8 matrix-remodelling associated 8 gene MP:0020941 decreased susceptibility to Togaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:31484075 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20210826 MGI 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20200402 MGI 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20210617 MGI PMID:33151556 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0001967 deafness IAGP N RGD:5509061 20210617 MGI PMID:33151556 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20210617 MGI PMID:33151556 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20210617 MGI PMID:33151556 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20210617 MGI PMID:33151556 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20210617 MGI PMID:33151556 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20210617 MGI PMID:33151556 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20211021 MGI 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20210617 MGI PMID:33151556 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20210617 MGI PMID:33151556 1550162 Baiap2l2 BAI1-associated protein 2-like 2 gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:33151556 1550163 Abtb1 ankyrin repeat and BTB domain containing 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1550163 Abtb1 ankyrin repeat and BTB domain containing 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1550163 Abtb1 ankyrin repeat and BTB domain containing 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1550163 Abtb1 ankyrin repeat and BTB domain containing 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1550163 Abtb1 ankyrin repeat and BTB domain containing 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1550163 Abtb1 ankyrin repeat and BTB domain containing 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210520 MGI 1550169 Asrgl1 asparaginase like 1 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20221222 MGI PMID:35118070 1550169 Asrgl1 asparaginase like 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20221222 MGI PMID:35118070 1550169 Asrgl1 asparaginase like 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20221222 MGI PMID:35118070 1550169 Asrgl1 asparaginase like 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20221222 MGI PMID:35118070 1550169 Asrgl1 asparaginase like 1 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20221222 MGI PMID:35118070 1550169 Asrgl1 asparaginase like 1 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20221222 MGI PMID:35118070 1550169 Asrgl1 asparaginase like 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20221222 MGI PMID:35118070 1550169 Asrgl1 asparaginase like 1 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20221222 MGI PMID:35118070 1550169 Asrgl1 asparaginase like 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20221222 MGI PMID:35118070 1550169 Asrgl1 asparaginase like 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20221222 MGI PMID:35118070 1550169 Asrgl1 asparaginase like 1 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20221222 MGI PMID:35118070 1550169 Asrgl1 asparaginase like 1 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20221222 MGI PMID:35118070 1550169 Asrgl1 asparaginase like 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20221222 MGI PMID:35118070 1550169 Asrgl1 asparaginase like 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20221222 MGI PMID:35118070 1550169 Asrgl1 asparaginase like 1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20221222 MGI PMID:35118070 1550171 Tpsg1 tryptase gamma 1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210401 MGI PMID:24821729 1550171 Tpsg1 tryptase gamma 1 gene MP:0010896 decreased lung compliance IAGP N RGD:5509061 20210401 MGI PMID:24821729 1550171 Tpsg1 tryptase gamma 1 gene MP:0010935 increased airway resistance IAGP N RGD:5509061 20210401 MGI PMID:24821729 1550171 Tpsg1 tryptase gamma 1 gene MP:0010950 abnormal lung hysteresivity IAGP N RGD:5509061 20210401 MGI PMID:24821729 1550171 Tpsg1 tryptase gamma 1 gene MP:0011044 increased lung elastance IAGP N RGD:5509061 20210401 MGI PMID:24821729 1550171 Tpsg1 tryptase gamma 1 gene MP:0011047 increased lung tissue damping IAGP N RGD:5509061 20210401 MGI PMID:24821729 1550171 Tpsg1 tryptase gamma 1 gene MP:0013299 decreased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20210401 MGI PMID:24821729 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18039842 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17599069 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:20005824 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20005824 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201022 MGI 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20005824 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:20005824 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20141003 MGI PMID:20005824 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12130538 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18039842 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:18039842 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12130538 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17599069 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17599069 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:17599069 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17599069 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:17599069 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25637356 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:20005824 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20421388 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:18039842 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:18039842 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:20005824 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:17599069 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:20421388 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:17599069 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:17599069 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:17599069 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12130538 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17599069 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20421388 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:20421388 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20421388 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:20421388 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:20421388 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20421388 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:20421388 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20005824 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20005824 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20005824 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20161013 MGI PMID:25637356 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18039842 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12130538 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550173 Ehmt2 euchromatic histone lysine N-methyltransferase 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1550175 Cyp4a14 cytochrome P450, family 4, subfamily a, polypeptide 14 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11320253 1550175 Cyp4a14 cytochrome P450, family 4, subfamily a, polypeptide 14 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11320253 1550175 Cyp4a14 cytochrome P450, family 4, subfamily a, polypeptide 14 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11320253 1550175 Cyp4a14 cytochrome P450, family 4, subfamily a, polypeptide 14 gene MP:0005529 abnormal renal vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:11320253 1550175 Cyp4a14 cytochrome P450, family 4, subfamily a, polypeptide 14 gene MP:0005531 increased renal vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:11320253 1550175 Cyp4a14 cytochrome P450, family 4, subfamily a, polypeptide 14 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11320253 1550175 Cyp4a14 cytochrome P450, family 4, subfamily a, polypeptide 14 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11320253 1550179 Srgn serglycin gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20200310 MGI PMID:15231821 1550179 Srgn serglycin gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15231821 1550181 Tubb3 tubulin, beta 3 class III gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:20074521 1550181 Tubb3 tubulin, beta 3 class III gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20074521 1550181 Tubb3 tubulin, beta 3 class III gene MP:0001061 abnormal oculomotor nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20074521 1550181 Tubb3 tubulin, beta 3 class III gene MP:0001063 abnormal trochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20074521 1550181 Tubb3 tubulin, beta 3 class III gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20074521 1550181 Tubb3 tubulin, beta 3 class III gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:20074521 1550181 Tubb3 tubulin, beta 3 class III gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:20074521 1550181 Tubb3 tubulin, beta 3 class III gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:20074521 1550181 Tubb3 tubulin, beta 3 class III gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:20074521 1550181 Tubb3 tubulin, beta 3 class III gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20074521 1550181 Tubb3 tubulin, beta 3 class III gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:20074521 1550181 Tubb3 tubulin, beta 3 class III gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20074521 1550182 Pde8a phosphodiesterase 8A gene MP:0002906 increased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20141003 MGI 1550182 Pde8a phosphodiesterase 8A gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20170105 MGI 1550182 Pde8a phosphodiesterase 8A gene MP:0003998 decreased thermal nociceptive threshold IEA N RGD:5509061 20141003 MGI 1550182 Pde8a phosphodiesterase 8A gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17172443 1550182 Pde8a phosphodiesterase 8A gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21187369 1550182 Pde8a phosphodiesterase 8A gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20170105 MGI 1550182 Pde8a phosphodiesterase 8A gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17172443 1550186 Clec2d C-type lectin domain family 2, member d gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:18782774 1550186 Clec2d C-type lectin domain family 2, member d gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20200310 MGI PMID:18782774 1550186 Clec2d C-type lectin domain family 2, member d gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20200310 MGI PMID:18782774 1550186 Clec2d C-type lectin domain family 2, member d gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20200310 MGI PMID:18782774 1550186 Clec2d C-type lectin domain family 2, member d gene MP:0003109 short femur IAGP N RGD:5509061 20200310 MGI PMID:18782774 1550186 Clec2d C-type lectin domain family 2, member d gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20200310 MGI PMID:18782774 1550186 Clec2d C-type lectin domain family 2, member d gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20200310 MGI PMID:18782774 1550186 Clec2d C-type lectin domain family 2, member d gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20200310 MGI PMID:18782774 1550186 Clec2d C-type lectin domain family 2, member d gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20200310 MGI PMID:18782774 1550186 Clec2d C-type lectin domain family 2, member d gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20200310 MGI PMID:18782774 1550186 Clec2d C-type lectin domain family 2, member d gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20200310 MGI PMID:18782774 1550186 Clec2d C-type lectin domain family 2, member d gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:18782774 1550186 Clec2d C-type lectin domain family 2, member d gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20200310 MGI PMID:18782774 1550187 Rnase13 ribonuclease, RNase A family, 13 (non-active) gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210520 MGI 1550187 Rnase13 ribonuclease, RNase A family, 13 (non-active) gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1550187 Rnase13 ribonuclease, RNase A family, 13 (non-active) gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1550187 Rnase13 ribonuclease, RNase A family, 13 (non-active) gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1550187 Rnase13 ribonuclease, RNase A family, 13 (non-active) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1550187 Rnase13 ribonuclease, RNase A family, 13 (non-active) gene MP:0003883 enlarged stomach IEA N RGD:5509061 20210520 MGI 1550187 Rnase13 ribonuclease, RNase A family, 13 (non-active) gene MP:0011875 absent stomach IEA N RGD:5509061 20210520 MGI 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9881978 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9881978 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:19349303 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9881978 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:9881978 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9881978 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19349303 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9881978 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9881978 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:9881978 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:14593101 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:17334369 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:17334369 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:17334369 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:14593101 1550192 Gcnt1 glucosaminyl (N-acetyl) transferase 1, core 2 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:17334369 1550193 Habp2 hyaluronic acid binding protein 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:22989567 1550193 Habp2 hyaluronic acid binding protein 2 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22989567 1550193 Habp2 hyaluronic acid binding protein 2 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:22989567 1550193 Habp2 hyaluronic acid binding protein 2 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22989567 1550196 Tigd3 tigger transposable element derived 3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1550196 Tigd3 tigger transposable element derived 3 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20221215 MGI 1550196 Tigd3 tigger transposable element derived 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1550196 Tigd3 tigger transposable element derived 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220519 MGI 1550198 Nipa1 non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human) gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20200310 MGI 1550199 Txnl1 thioredoxin-like 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230119 MGI 1550199 Txnl1 thioredoxin-like 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20230119 MGI 1550199 Txnl1 thioredoxin-like 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 1550199 Txnl1 thioredoxin-like 1 gene MP:0001340 abnormal eyelid morphology IEA N RGD:5509061 20230119 MGI 1550199 Txnl1 thioredoxin-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230126 MGI PMID:19349280 1550199 Txnl1 thioredoxin-like 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1550199 Txnl1 thioredoxin-like 1 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20230119 MGI 1550199 Txnl1 thioredoxin-like 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1550199 Txnl1 thioredoxin-like 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1550199 Txnl1 thioredoxin-like 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230119 MGI 1550200 Panx2 pannexin 2 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1550200 Panx2 pannexin 2 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:22147915 1550200 Panx2 pannexin 2 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20181227 MGI 1550200 Panx2 pannexin 2 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1550200 Panx2 pannexin 2 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:22147915 1550200 Panx2 pannexin 2 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:22147915 1550200 Panx2 pannexin 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1550200 Panx2 pannexin 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1550205 Tyw1 tRNA-yW synthesizing protein 1 homolog (S. cerevisiae) gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1550205 Tyw1 tRNA-yW synthesizing protein 1 homolog (S. cerevisiae) gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1550205 Tyw1 tRNA-yW synthesizing protein 1 homolog (S. cerevisiae) gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20210128 MGI 1550205 Tyw1 tRNA-yW synthesizing protein 1 homolog (S. cerevisiae) gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1550205 Tyw1 tRNA-yW synthesizing protein 1 homolog (S. cerevisiae) gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1550205 Tyw1 tRNA-yW synthesizing protein 1 homolog (S. cerevisiae) gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1550205 Tyw1 tRNA-yW synthesizing protein 1 homolog (S. cerevisiae) gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20201022 MGI 1550206 Ttc17 tetratricopeptide repeat domain 17 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230601 MGI 1550206 Ttc17 tetratricopeptide repeat domain 17 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1550206 Ttc17 tetratricopeptide repeat domain 17 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230601 MGI 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20150910 MGI PMID:18952847 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10209122 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20181129 MGI PMID:17419998 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20150910 MGI PMID:18952847 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21514245 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:21514245 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17419998 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:17419998 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:17419998 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001215 skin hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17419998 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17419998 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17419998 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20150910 MGI PMID:18952847 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:17419998 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10209122 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:16887817 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10209122 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:16887817 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001717 absent ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:19219045 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:10209122 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19219045 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20220203 MGI PMID:21527500 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220203 MGI PMID:21527500 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220203 MGI PMID:21527500 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21514245 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19219045 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:17419998 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20150910 MGI PMID:18952847 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20150910 MGI PMID:18952847 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:17419998 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:10209122 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:10209122 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10209122 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:16887817 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20220203 MGI PMID:21527500 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19219045 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20220203 MGI PMID:21527500 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:23945236 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0008526 decreased cranium width IAGP N RGD:5509061 20180621 MGI PMID:29590634 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21514245 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10209122 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17419998 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0009819 abnormal circulating androgen level IAGP N RGD:5509061 20220203 MGI PMID:21527500 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0009905 absent tongue IAGP N RGD:5509061 20150910 MGI PMID:18952847 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20180621 MGI PMID:29590634 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17419998 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0010283 decreased classified tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21514245 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0010457 pulmonary artery stenosis IAGP N RGD:5509061 20180621 MGI PMID:29590634 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17419998 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16887817 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19219045 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10209122 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20220203 MGI PMID:21527500 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0011812 increased cranium length IAGP N RGD:5509061 20180621 MGI PMID:29590634 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20180621 MGI PMID:29590634 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0012065 increased astrocyte number IAGP N RGD:5509061 20180621 MGI PMID:29590634 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:10209122 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0014269 decreased testes secretion IAGP N RGD:5509061 20230810 MGI PMID:21527500 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0030166 increased inner canthal distance IAGP N RGD:5509061 20180621 MGI PMID:29590634 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0030575 decreased hair follicle cell proliferation IAGP N RGD:5509061 20181129 MGI PMID:17419998 1550208 Map2k1 mitogen-activated protein kinase kinase 1 gene MP:0031436 decreased copulatory plug deposition IAGP N RGD:5509061 20220922 MGI PMID:21527500 1550211 Cdk19 cyclin dependent kinase 19 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1550211 Cdk19 cyclin dependent kinase 19 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20220428 MGI PMID:35110726 1550211 Cdk19 cyclin dependent kinase 19 gene MP:0010052 increased grip strength IEA N RGD:5509061 20200310 MGI 1550211 Cdk19 cyclin dependent kinase 19 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20220428 MGI PMID:35110726 1550211 Cdk19 cyclin dependent kinase 19 gene MP:0011903 decreased hematopoietic stem cell proliferation IAGP N RGD:5509061 20220428 MGI PMID:35110726 1550211 Cdk19 cyclin dependent kinase 19 gene MP:0013705 decreased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20220428 MGI PMID:35110726 1550212 Best3 bestrophin 3 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0002083 premature death IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0004044 aortic dissection IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0010139 aortitis IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0010470 dilated ascending aorta IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0010473 descending aorta dilation IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0010658 thoracic aorta aneurysm IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0010659 abdominal aorta aneurysm IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550212 Best3 bestrophin 3 gene MP:0010997 decreased aorta wall thickness IAGP N RGD:5509061 20231019 MGI PMID:37203562 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20200310 MGI PMID:30738849 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20240328 MGI PMID:939824 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20200310 MGI PMID:30738849 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0000588 thick tail IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0000592 short tail IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0001147 small testis IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:25762570 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20240523 MGI PMID:3593827 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:25762570 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20200310 MGI PMID:25762570 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20200310 MGI PMID:30738849 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20240523 MGI PMID:3593827 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0002673 abnormal sperm number IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20200310 MGI PMID:30738849 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0003956 abnormal body size IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20200310 MGI PMID:30738849 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20200310 MGI PMID:30738849 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0004355 short radius IAGP N RGD:5509061 20200310 MGI PMID:30738849 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20200310 MGI PMID:30738849 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0004635 short metatarsal bones IAGP N RGD:5509061 20200310 MGI PMID:30738849 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20240328 MGI PMID:939824 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20240328 MGI PMID:5713631 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0009856 failure of ejaculation IAGP N RGD:5509061 20240523 MGI PMID:3593827 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0010943 abnormal bronchus epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:25762570 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20200310 MGI PMID:30738849 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0014274 decreased respiration IAGP N RGD:5509061 20230810 MGI PMID:25762570 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0030775 abnormal calcaneal tendon morphology IAGP N RGD:5509061 20200310 MGI PMID:30738849 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0030803 abnormal tendon cell morphology IAGP N RGD:5509061 20200310 MGI PMID:30738849 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0031628 abnormal intromission IAGP N RGD:5509061 20240711 MGI PMID:3593827 1550215 Adamtsl2 ADAMTS-like 2 gene MP:0031646 impotence IAGP N RGD:5509061 20240822 MGI PMID:3593827 1550216 Matn1 matrilin 1, cartilage matrix protein gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1550216 Matn1 matrilin 1, cartilage matrix protein gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1550216 Matn1 matrilin 1, cartilage matrix protein gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10633862 1550216 Matn1 matrilin 1, cartilage matrix protein gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1550216 Matn1 matrilin 1, cartilage matrix protein gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1550216 Matn1 matrilin 1, cartilage matrix protein gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20210812 MGI PMID:27573814 1550216 Matn1 matrilin 1, cartilage matrix protein gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20210812 MGI PMID:27573814 1550216 Matn1 matrilin 1, cartilage matrix protein gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20210812 MGI PMID:27573814 1550217 Trrap transformation/transcription domain-associated protein gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20160804 MGI 1550217 Trrap transformation/transcription domain-associated protein gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11544477 1550217 Trrap transformation/transcription domain-associated protein gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11544477 1550217 Trrap transformation/transcription domain-associated protein gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1550217 Trrap transformation/transcription domain-associated protein gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:11544477 1550217 Trrap transformation/transcription domain-associated protein gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11544477 1550217 Trrap transformation/transcription domain-associated protein gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11544477 1550217 Trrap transformation/transcription domain-associated protein gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20160804 MGI 1550217 Trrap transformation/transcription domain-associated protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11544477 1550217 Trrap transformation/transcription domain-associated protein gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11544477 1550217 Trrap transformation/transcription domain-associated protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550218 Hamp hepcidin antimicrobial peptide gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:16574947 1550218 Hamp hepcidin antimicrobial peptide gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20200310 MGI PMID:24646470 1550218 Hamp hepcidin antimicrobial peptide gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:16574947 1550218 Hamp hepcidin antimicrobial peptide gene MP:0004152 abnormal circulating iron level IAGP N RGD:5509061 20200310 MGI PMID:16574947 1550218 Hamp hepcidin antimicrobial peptide gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20200310 MGI PMID:16574947 1550218 Hamp hepcidin antimicrobial peptide gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20200310 MGI PMID:24646470 1550218 Hamp hepcidin antimicrobial peptide gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20200310 MGI PMID:16574947 1550218 Hamp hepcidin antimicrobial peptide gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20200310 MGI PMID:20053755 1550218 Hamp hepcidin antimicrobial peptide gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20200310 MGI PMID:24646470 1550218 Hamp hepcidin antimicrobial peptide gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:23390527 1550218 Hamp hepcidin antimicrobial peptide gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20200310 MGI PMID:16574947 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11675330 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:15484191 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0001405 impaired coordination IEA N RGD:5509061 20111116 MGI 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:18439426 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11675330 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15484191 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:17548595 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:18439426 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11675330 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11884450 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11675330 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11675330 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:17548595 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230720 MGI 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11675330 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0008345 abnormal gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17548595 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11884450 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0008349 abnormal gamma-delta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11884450 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:17548595 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:18439426 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0008363 decreased CD8-positive, gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:11884450 1550219 Ccr9 C-C motif chemokine receptor 9 gene MP:0008399 abnormal alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18439426 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20111116 MGI 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0002084 abnormal developmental patterning IEA N RGD:5509061 20111116 MGI 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20190912 MGI PMID:30872163 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20190912 MGI PMID:30872163 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20190912 MGI PMID:30872163 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0004180 failure of initiation of embryo turning IEA N RGD:5509061 20111116 MGI 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0004187 cardia bifida IEA N RGD:5509061 20111116 MGI 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20190912 MGI PMID:30872163 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0008762 embryonic lethality IEA N RGD:5509061 20111116 MGI 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20190912 MGI PMID:30872163 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20190912 MGI PMID:30872163 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1550222 Alg13 asparagine-linked glycosylation 13 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1550230 Tnfrsf12a tumor necrosis factor receptor superfamily, member 12a gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16424220 1550230 Tnfrsf12a tumor necrosis factor receptor superfamily, member 12a gene MP:0010042 abnormal oval cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16110324 1550234 Senp7 SUMO1/sentrin specific peptidase 7 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1550234 Senp7 SUMO1/sentrin specific peptidase 7 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200310 MGI 1550238 Fbxl12 F-box and leucine-rich repeat protein 12 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160818 MGI PMID:26124079 1550238 Fbxl12 F-box and leucine-rich repeat protein 12 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160818 MGI PMID:26124079 1550238 Fbxl12 F-box and leucine-rich repeat protein 12 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20160818 MGI PMID:26124079 1550238 Fbxl12 F-box and leucine-rich repeat protein 12 gene MP:0004259 small placenta IAGP N RGD:5509061 20160818 MGI PMID:26124079 1550238 Fbxl12 F-box and leucine-rich repeat protein 12 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20160818 MGI PMID:26124079 1550238 Fbxl12 F-box and leucine-rich repeat protein 12 gene MP:0008957 abnormal placenta junctional zone morphology IAGP N RGD:5509061 20160818 MGI PMID:26124079 1550238 Fbxl12 F-box and leucine-rich repeat protein 12 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20160818 MGI PMID:26124079 1550238 Fbxl12 F-box and leucine-rich repeat protein 12 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20160818 MGI PMID:26124079 1550238 Fbxl12 F-box and leucine-rich repeat protein 12 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160818 MGI PMID:26124079 1550238 Fbxl12 F-box and leucine-rich repeat protein 12 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20160818 MGI PMID:26124079 1550240 Septin5 septin 5 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1550240 Septin5 septin 5 gene MP:0000692 small spleen IEA N RGD:5509061 20200402 MGI 1550240 Septin5 septin 5 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1550240 Septin5 septin 5 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19240081 1550240 Septin5 septin 5 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19240081 1550240 Septin5 septin 5 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:19240081 1550240 Septin5 septin 5 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:19240081 1550240 Septin5 septin 5 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1550240 Septin5 septin 5 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20200402 MGI 1550240 Septin5 septin 5 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1550240 Septin5 septin 5 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20200402 MGI 1550240 Septin5 septin 5 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:11880646 1550240 Septin5 septin 5 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:19240081 1550240 Septin5 septin 5 gene MP:0009586 increased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:11880646 1550240 Septin5 septin 5 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1550240 Septin5 septin 5 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1550241 Ankle1 ankyrin repeat and LEM domain containing 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1550241 Ankle1 ankyrin repeat and LEM domain containing 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200310 MGI 1550241 Ankle1 ankyrin repeat and LEM domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:27010503 1550241 Ankle1 ankyrin repeat and LEM domain containing 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:27010503 1550247 Wdr36 WD repeat domain 36 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1550247 Wdr36 WD repeat domain 36 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20200310 MGI PMID:21051332 1550247 Wdr36 WD repeat domain 36 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220811 MGI 1550247 Wdr36 WD repeat domain 36 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1550247 Wdr36 WD repeat domain 36 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21051332 1550247 Wdr36 WD repeat domain 36 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550247 Wdr36 WD repeat domain 36 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1550247 Wdr36 WD repeat domain 36 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1550249 Cd2ap CD2-associated protein gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:10514378 1550249 Cd2ap CD2-associated protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10514378 1550249 Cd2ap CD2-associated protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20201217 MGI PMID:30612599 1550249 Cd2ap CD2-associated protein gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20201217 MGI PMID:30612599 1550249 Cd2ap CD2-associated protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10514378 1550249 Cd2ap CD2-associated protein gene MP:0002083 premature death IAGP N RGD:5509061 20201217 MGI PMID:30612599 1550249 Cd2ap CD2-associated protein gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:12764198 1550249 Cd2ap CD2-associated protein gene MP:0002871 albuminuria IAGP N RGD:5509061 20201217 MGI PMID:30612599 1550249 Cd2ap CD2-associated protein gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:10514378 1550249 Cd2ap CD2-associated protein gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20201217 MGI PMID:30612599 1550249 Cd2ap CD2-associated protein gene MP:0003606 kidney failure IAGP N RGD:5509061 20201217 MGI PMID:30612599 1550249 Cd2ap CD2-associated protein gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:10514378 1550249 Cd2ap CD2-associated protein gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:10514378 1550249 Cd2ap CD2-associated protein gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10514378 1550249 Cd2ap CD2-associated protein gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:12764198 1550249 Cd2ap CD2-associated protein gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:10514378 1550249 Cd2ap CD2-associated protein gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20201217 MGI PMID:30612599 1550249 Cd2ap CD2-associated protein gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:10514378 1550249 Cd2ap CD2-associated protein gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12764198 1550249 Cd2ap CD2-associated protein gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10514378 1550249 Cd2ap CD2-associated protein gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12764198 1550249 Cd2ap CD2-associated protein gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:10514378 1550249 Cd2ap CD2-associated protein gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20201217 MGI PMID:30612599 1550249 Cd2ap CD2-associated protein gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:10514378 1550249 Cd2ap CD2-associated protein gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20201217 MGI PMID:30612599 1550249 Cd2ap CD2-associated protein gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:10514378 1550249 Cd2ap CD2-associated protein gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20201217 MGI PMID:30612599 1550249 Cd2ap CD2-associated protein gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1550249 Cd2ap CD2-associated protein gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10514378 1550249 Cd2ap CD2-associated protein gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20201217 MGI PMID:30612599 1550249 Cd2ap CD2-associated protein gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:12764198 1550249 Cd2ap CD2-associated protein gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:10514378 1550249 Cd2ap CD2-associated protein gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:12764198 1550251 Klhdc8b kelch domain containing 8B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 1550252 Snx33 sorting nexin 33 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1550252 Snx33 sorting nexin 33 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1550253 Adgrg5 adhesion G protein-coupled receptor G5 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1550253 Adgrg5 adhesion G protein-coupled receptor G5 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1550254 Ddx19a DEAD box helicase 19a gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210506 MGI PMID:30699353 1550257 Mon1a MON1 homolog A, secretory traffciking associated gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 1550257 Mon1a MON1 homolog A, secretory traffciking associated gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20220519 MGI 1550257 Mon1a MON1 homolog A, secretory traffciking associated gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1550262 Ppp2r1a protein phosphatase 2, regulatory subunit A, alpha gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21791616 1550262 Ppp2r1a protein phosphatase 2, regulatory subunit A, alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21791616 1550262 Ppp2r1a protein phosphatase 2, regulatory subunit A, alpha gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:21791616 1550262 Ppp2r1a protein phosphatase 2, regulatory subunit A, alpha gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21791616 1550262 Ppp2r1a protein phosphatase 2, regulatory subunit A, alpha gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21791616 1550262 Ppp2r1a protein phosphatase 2, regulatory subunit A, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21791616 1550262 Ppp2r1a protein phosphatase 2, regulatory subunit A, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21791616 1550262 Ppp2r1a protein phosphatase 2, regulatory subunit A, alpha gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:21791616 1550262 Ppp2r1a protein phosphatase 2, regulatory subunit A, alpha gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21791616 1550262 Ppp2r1a protein phosphatase 2, regulatory subunit A, alpha gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21791616 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20240321 MGI PMID:37228654 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20240321 MGI PMID:37228654 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20240321 MGI PMID:37228654 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20240321 MGI PMID:37228654 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20240321 MGI PMID:37228654 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0011261 abnormal limb mesenchyme morphology IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0011685 abnormal limb paddle morphology IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20240321 MGI PMID:37228654 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20240321 MGI PMID:37228654 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0013213 abnormal embryonic neuroepithelium primary cilium morphology IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550264 Dync2i2 dynein 2 intermediate chain 2 gene MP:0020850 abnormal microtubule cytoskeleton morphology IAGP N RGD:5509061 20210225 MGI PMID:28379358 1550265 Idh3b isocitrate dehydrogenase 3 (NAD+) beta gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1550265 Idh3b isocitrate dehydrogenase 3 (NAD+) beta gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1550265 Idh3b isocitrate dehydrogenase 3 (NAD+) beta gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1550265 Idh3b isocitrate dehydrogenase 3 (NAD+) beta gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1550265 Idh3b isocitrate dehydrogenase 3 (NAD+) beta gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1550265 Idh3b isocitrate dehydrogenase 3 (NAD+) beta gene MP:0002574 increased vertical activity IEA N RGD:5509061 20201022 MGI 1550266 Pgf placental growth factor gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17003333 1550266 Pgf placental growth factor gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11329059 1550266 Pgf placental growth factor gene MP:0001619 abnormal vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:12150967 1550266 Pgf placental growth factor gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:11329059 1550266 Pgf placental growth factor gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:11329059 1550266 Pgf placental growth factor gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:17003333 1550266 Pgf placental growth factor gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:17051153 1550266 Pgf placental growth factor gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:12393422 1550266 Pgf placental growth factor gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17003333 1550266 Pgf placental growth factor gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:17003333 1550266 Pgf placental growth factor gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17003333 1550266 Pgf placental growth factor gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:17003333 1550266 Pgf placental growth factor gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17003333 1550266 Pgf placental growth factor gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:17003333 1550269 Fnbp1l formin binding protein 1-like gene MP:0002175 decreased brain weight IEA N RGD:5509061 20220519 MGI 1550269 Fnbp1l formin binding protein 1-like gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1550269 Fnbp1l formin binding protein 1-like gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1550269 Fnbp1l formin binding protein 1-like gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1550271 Arrdc3 arrestin domain containing 3 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:23236378 1550271 Arrdc3 arrestin domain containing 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23236378 1550271 Arrdc3 arrestin domain containing 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0003213 decreased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0003213 decreased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:23236378 1550271 Arrdc3 arrestin domain containing 3 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0005661 decreased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21982743 1550271 Arrdc3 arrestin domain containing 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23236378 1550271 Arrdc3 arrestin domain containing 3 gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20180125 MGI PMID:21982743 1550273 Smad5 SMAD family member 5 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:14502571 1550273 Smad5 SMAD family member 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10677256 1550273 Smad5 SMAD family member 5 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:14502571 1550273 Smad5 SMAD family member 5 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:14502571 1550273 Smad5 SMAD family member 5 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:14502571 1550273 Smad5 SMAD family member 5 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20220630 MGI PMID:35383354 1550273 Smad5 SMAD family member 5 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10677256 1550273 Smad5 SMAD family member 5 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10677256 1550273 Smad5 SMAD family member 5 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:14502571 1550273 Smad5 SMAD family member 5 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:14502571 1550273 Smad5 SMAD family member 5 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:14502571 1550273 Smad5 SMAD family member 5 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20220630 MGI PMID:35383354 1550273 Smad5 SMAD family member 5 gene MP:0001749 suppressed circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:19819941 1550273 Smad5 SMAD family member 5 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:11404080 1550273 Smad5 SMAD family member 5 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220630 MGI PMID:35383354 1550273 Smad5 SMAD family member 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17967875 1550273 Smad5 SMAD family member 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20220630 MGI PMID:35383354 1550273 Smad5 SMAD family member 5 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11404080 1550273 Smad5 SMAD family member 5 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220630 MGI PMID:35383354 1550273 Smad5 SMAD family member 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19819941 1550273 Smad5 SMAD family member 5 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:14502571 1550273 Smad5 SMAD family member 5 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14502571 1550273 Smad5 SMAD family member 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14502571 1550273 Smad5 SMAD family member 5 gene MP:0002208 abnormal germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0002976 vascular smooth muscle hypotrophy IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17967875 1550273 Smad5 SMAD family member 5 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220630 MGI PMID:35383354 1550273 Smad5 SMAD family member 5 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:14502571 1550273 Smad5 SMAD family member 5 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:14502571 1550273 Smad5 SMAD family member 5 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:10677256 1550273 Smad5 SMAD family member 5 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:17456754 1550273 Smad5 SMAD family member 5 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:14502571 1550273 Smad5 SMAD family member 5 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17456754 1550273 Smad5 SMAD family member 5 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:17967875 1550273 Smad5 SMAD family member 5 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17967875 1550273 Smad5 SMAD family member 5 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17967875 1550273 Smad5 SMAD family member 5 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:11404080 1550273 Smad5 SMAD family member 5 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0008393 absent primordial germ cells IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:17967875 1550273 Smad5 SMAD family member 5 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20220630 MGI PMID:35383354 1550273 Smad5 SMAD family member 5 gene MP:0009649 delayed embryo implantation IAGP N RGD:5509061 20220630 MGI PMID:35383354 1550273 Smad5 SMAD family member 5 gene MP:0009656 delayed chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20220630 MGI PMID:35383354 1550273 Smad5 SMAD family member 5 gene MP:0009662 abnormal uterine receptivity IAGP N RGD:5509061 20220630 MGI PMID:35383354 1550273 Smad5 SMAD family member 5 gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20220630 MGI PMID:35383354 1550273 Smad5 SMAD family member 5 gene MP:0010642 absent third pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:16765933 1550273 Smad5 SMAD family member 5 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:10079226 1550273 Smad5 SMAD family member 5 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:10677256 1550273 Smad5 SMAD family member 5 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:17456754 1550273 Smad5 SMAD family member 5 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:10079220 1550273 Smad5 SMAD family member 5 gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19819941 1550274 Trappc4 trafficking protein particle complex 4 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1550274 Trappc4 trafficking protein particle complex 4 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20231207 MGI 1550274 Trappc4 trafficking protein particle complex 4 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20231207 MGI 1550274 Trappc4 trafficking protein particle complex 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0001260 increased body weight IAGP N RGD:5509061 20151126 MGI PMID:24966089 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:20178979 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:22184322 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20151126 MGI PMID:24966089 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:22184322 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20141003 MGI PMID:22184322 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:22184322 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0005633 increased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:22184322 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20151126 MGI PMID:24966089 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:22184322 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20151126 MGI PMID:24966089 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0011131 abnormal lung endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20178979 1550275 Cyp2c23 cytochrome P450, family 2, subfamily c, polypeptide 23 gene MP:0011140 decreased lung endothelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20178979 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0009925 increased transitional stage T2 B cell number IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0013802 abnormal IgG2 level IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0014351 abnormal spleen B cell follicle shape IAGP N RGD:5509061 20240104 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0020174 abnormal IgG level IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550278 Adgrg3 adhesion G protein-coupled receptor G3 gene MP:0020175 abnormal IgG1 level IAGP N RGD:5509061 20160218 MGI PMID:24113187 1550281 Mical3 microtubule associated monooxygenase, calponin and LIM domain containing 3 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1550281 Mical3 microtubule associated monooxygenase, calponin and LIM domain containing 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1550281 Mical3 microtubule associated monooxygenase, calponin and LIM domain containing 3 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1550281 Mical3 microtubule associated monooxygenase, calponin and LIM domain containing 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1550281 Mical3 microtubule associated monooxygenase, calponin and LIM domain containing 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1550281 Mical3 microtubule associated monooxygenase, calponin and LIM domain containing 3 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:16877546 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:16484321 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:16877546 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:14745012 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16877546 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17142319 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17591950 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19838304 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001147 small testis IAGP N RGD:5509061 20200820 MGI PMID:31779270 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:17591950 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:19838304 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20220616 MGI PMID:26265072 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:14745012 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:17591950 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:19574395 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:19838304 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20220616 MGI PMID:26265072 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:16484321 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220616 MGI PMID:26265072 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:14745012 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17591950 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19574395 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220616 MGI PMID:26265072 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15107499 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19838304 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220811 MGI PMID:35574006 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230119 MGI 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:14745012 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15107499 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:15107499 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:21163256 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20160526 MGI PMID:24803656 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15107499 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16484321 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16877546 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17142319 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17591950 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19574395 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20220616 MGI PMID:26265072 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20220811 MGI PMID:35574006 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:17142319 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21163256 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:16877546 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15107499 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16484321 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16877546 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17142319 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19838304 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20160526 MGI PMID:24803656 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20200820 MGI PMID:31779270 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21163256 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200820 MGI PMID:31779270 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002776 increased Sertoli cell number IAGP N RGD:5509061 20141003 MGI PMID:17591950 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002776 increased Sertoli cell number IAGP N RGD:5509061 20160526 MGI PMID:24803656 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:15107499 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17142319 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:18243172 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002782 abnormal testes secretion IAGP N RGD:5509061 20141003 MGI PMID:18243172 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17591950 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22829911 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15919750 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16877546 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19574395 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230119 MGI 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22829911 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20141003 MGI PMID:16877546 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20141003 MGI PMID:18243172 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20141003 MGI PMID:21163256 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:14745012 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15107499 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15919750 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16484321 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17591950 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19574395 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21163256 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220616 MGI PMID:26265072 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:14745012 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:15107499 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:17591950 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:19838304 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:21163256 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220616 MGI PMID:26265072 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:14745012 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230119 MGI 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:14745012 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:15107499 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:17142319 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:17591950 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220616 MGI PMID:26265072 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220811 MGI PMID:35574006 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:19838304 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20200820 MGI PMID:31779270 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20220811 MGI PMID:35574006 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0005287 narrow eye opening IEA N RGD:5509061 20230119 MGI 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:15919750 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0005542 cornea vascularization IEA N RGD:5509061 20230119 MGI 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0006241 abnormal placement of pupils IEA N RGD:5509061 20230119 MGI 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0006307 abnormal seminiferous tubule size IAGP N RGD:5509061 20141003 MGI PMID:18243172 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0006308 enlarged seminiferous tubules IAGP N RGD:5509061 20200820 MGI PMID:31779270 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:17591950 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20220616 MGI PMID:26265072 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14745012 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220616 MGI PMID:26265072 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:14745012 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17591950 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:21163256 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0006418 abnormal testis cord formation IAGP N RGD:5509061 20200820 MGI PMID:31779270 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0006428 ectopic Sertoli cells IAGP N RGD:5509061 20141003 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0006428 ectopic Sertoli cells IAGP N RGD:5509061 20200820 MGI PMID:31779270 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:14745012 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:15107499 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17142319 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22829911 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230119 MGI 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18243172 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220616 MGI PMID:26265072 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20230119 MGI 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0013598 Leydig cell hypertrophy IAGP N RGD:5509061 20150319 MGI PMID:19574395 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20150312 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20150312 MGI PMID:21163256 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220616 MGI PMID:26265072 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:14745012 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:19071104 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0020142 increased anti-sperm antibody level IAGP N RGD:5509061 20160616 MGI PMID:24803656 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0020355 abnormal Sertoli cell barrier morphology IAGP N RGD:5509061 20220616 MGI PMID:26265072 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0020356 abnormal Sertoli cell barrier function IAGP N RGD:5509061 20160915 MGI PMID:24803656 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0020356 abnormal Sertoli cell barrier function IAGP N RGD:5509061 20220616 MGI PMID:26265072 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0020847 abnormal peroxisome physiology IAGP N RGD:5509061 20230615 MGI PMID:22829911 1550285 Plekha5 pleckstrin homology domain containing, family A member 5 gene MP:0031407 increased Sertoli cell proliferation IAGP N RGD:5509061 20220630 MGI PMID:19071104 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20200310 MGI PMID:15634781 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0000292 distended pericardium IAGP N RGD:5509061 20200310 MGI PMID:15634781 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0000292 distended pericardium IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200402 MGI 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20200310 MGI PMID:15634781 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200310 MGI 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:15634781 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:15634781 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20200310 MGI PMID:15634781 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20200310 MGI PMID:15634781 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20200310 MGI 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15634781 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20201231 MGI 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0011732 decreased somite size IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20200310 MGI PMID:15665098 1550286 Aph1a aph1 homolog A, gamma secretase subunit gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:16505171 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:17183677 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12529747 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12933578 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12529747 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:12529747 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0004898 uterine hemorrhage IAGP N RGD:5509061 20150827 MGI PMID:12933578 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0004898 uterine hemorrhage IAGP N RGD:5509061 20150827 MGI PMID:17183677 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0004898 uterine hemorrhage IAGP N RGD:5509061 20150827 MGI PMID:18224415 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:12529747 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:12933578 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:12529747 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:12529747 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20150827 MGI PMID:18224415 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:12529747 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20150827 MGI PMID:12933578 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20150827 MGI PMID:18224415 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:12529747 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16505171 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17183677 1550288 F13a1 coagulation factor XIII, A1 subunit gene MP:0031152 subcutaneous hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:12529747 1550289 Msx3 msh homeobox 3 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20231207 MGI 1550289 Msx3 msh homeobox 3 gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20220519 MGI 1550294 Rcor1 REST corepressor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:24652990 1550294 Rcor1 REST corepressor 1 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20200310 MGI PMID:24652990 1550294 Rcor1 REST corepressor 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20200310 MGI PMID:24652990 1550294 Rcor1 REST corepressor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24652990 1550294 Rcor1 REST corepressor 1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24652990 1550296 Taok2 TAO kinase 2 gene MP:0001265 decreased body size IEA N RGD:5509061 20200310 MGI 1550296 Taok2 TAO kinase 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1550296 Taok2 TAO kinase 2 gene MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20200310 MGI PMID:22883308 1550296 Taok2 TAO kinase 2 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20200310 MGI PMID:22883308 1550296 Taok2 TAO kinase 2 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20200310 MGI PMID:22883308 1550296 Taok2 TAO kinase 2 gene MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20200310 MGI PMID:22883308 1550296 Taok2 TAO kinase 2 gene MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20200310 MGI PMID:22883308 1550296 Taok2 TAO kinase 2 gene MP:0011617 abnormal habituation IAGP N RGD:5509061 20200310 MGI PMID:22883308 1550296 Taok2 TAO kinase 2 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20200310 MGI PMID:22883308 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20210520 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0001706 abnormal left-right axis patterning IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0001726 abnormal allantois morphology IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0002824 abnormal chorioallantoic fusion IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0002861 abnormal tail bud morphology IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20211021 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0003896 prolonged PR interval IEA N RGD:5509061 20221215 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0009806 abnormal otic vesicle morphology IEA N RGD:5509061 20190502 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20211021 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1550299 Pigq phosphatidylinositol glycan anchor biosynthesis, class Q gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1550300 Ift80 intraflagellar transport 80 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20200310 MGI PMID:21227999 1550300 Ift80 intraflagellar transport 80 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20200310 MGI PMID:21227999 1550300 Ift80 intraflagellar transport 80 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20200310 MGI PMID:21227999 1550300 Ift80 intraflagellar transport 80 gene MP:0000552 abnormal radius morphology IEA N RGD:5509061 20201231 MGI 1550300 Ift80 intraflagellar transport 80 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:26053317 1550300 Ift80 intraflagellar transport 80 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:21227999 1550300 Ift80 intraflagellar transport 80 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20200310 MGI PMID:21227999 1550300 Ift80 intraflagellar transport 80 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20200310 MGI 1550300 Ift80 intraflagellar transport 80 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20200310 MGI PMID:21227999 1550300 Ift80 intraflagellar transport 80 gene MP:0005108 abnormal ulna morphology IEA N RGD:5509061 20201231 MGI 1550300 Ift80 intraflagellar transport 80 gene MP:0005352 small cranium IAGP N RGD:5509061 20200310 MGI PMID:21227999 1550300 Ift80 intraflagellar transport 80 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1550300 Ift80 intraflagellar transport 80 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20200310 MGI PMID:21227999 1550300 Ift80 intraflagellar transport 80 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20200310 MGI PMID:21227999 1550300 Ift80 intraflagellar transport 80 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20200310 MGI PMID:21227999 1550300 Ift80 intraflagellar transport 80 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1550300 Ift80 intraflagellar transport 80 gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20200310 MGI PMID:21227999 1550300 Ift80 intraflagellar transport 80 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21227999 1550300 Ift80 intraflagellar transport 80 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21227999 1550300 Ift80 intraflagellar transport 80 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1550300 Ift80 intraflagellar transport 80 gene MP:0013206 abnormal motile cilium morphology IAGP N RGD:5509061 20200310 MGI PMID:26053317 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21216955 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0001194 dermatitis IAGP N RGD:5509061 20230601 MGI PMID:24371506 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:21878566 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20111116 MGI 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0001405 impaired coordination IEA N RGD:5509061 20111116 MGI 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:21878566 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0001412 excessive scratching IAGP N RGD:5509061 20230601 MGI PMID:24371506 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:21878566 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21216955 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:24218620 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20160609 MGI PMID:25368181 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21216955 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:21832054 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:20190743 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:15146240 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21521762 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21665954 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002083 premature death IAGP N RGD:5509061 20230601 MGI PMID:24371506 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10973973 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20230601 MGI PMID:24371506 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15146240 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:15146240 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12881419 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20220811 MGI 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20111116 MGI 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21216955 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002833 increased heart weight IAGP N RGD:5509061 20160609 MGI PMID:25368181 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:24218620 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:12881419 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20141003 MGI PMID:24218620 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20160609 MGI PMID:25368181 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:21216955 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12881419 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15146240 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21665954 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:24218620 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:15146240 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:21216955 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:21832054 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:24218620 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20160609 MGI PMID:25368181 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20160609 MGI PMID:25368181 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:21216955 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:24218620 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21224388 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21521762 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:24218620 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160609 MGI PMID:25368181 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12881419 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:21832054 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12881419 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:21216955 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:21521762 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:18174367 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:20190743 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20230601 MGI PMID:24371506 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21878566 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0009455 enhanced cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21878566 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21832054 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21878566 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21216955 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10973973 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21216955 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20160609 MGI PMID:25368181 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0012557 decreased calcium uptake by cardiac muscle IAGP N RGD:5509061 20160609 MGI PMID:25368181 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:21878566 1550302 Cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1550306 Kat5 K(lysine) acetyltransferase 5 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17728759 1550306 Kat5 K(lysine) acetyltransferase 5 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17728759 1550306 Kat5 K(lysine) acetyltransferase 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17728759 1550306 Kat5 K(lysine) acetyltransferase 5 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20190502 MGI 1550306 Kat5 K(lysine) acetyltransferase 5 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17728759 1550306 Kat5 K(lysine) acetyltransferase 5 gene MP:0006204 embryonic lethality before implantation IAGP N RGD:5509061 20141003 MGI PMID:17728759 1550306 Kat5 K(lysine) acetyltransferase 5 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:17728759 1550306 Kat5 K(lysine) acetyltransferase 5 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:17728759 1550306 Kat5 K(lysine) acetyltransferase 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550306 Kat5 K(lysine) acetyltransferase 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1550306 Kat5 K(lysine) acetyltransferase 5 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1550307 Paqr8 progestin and adipoQ receptor family member VIII gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1550307 Paqr8 progestin and adipoQ receptor family member VIII gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 1550313 Lrrfip1 leucine rich repeat (in FLII) interacting protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1550313 Lrrfip1 leucine rich repeat (in FLII) interacting protein 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1550314 Ociad1 OCIA domain containing 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1550314 Ociad1 OCIA domain containing 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1550314 Ociad1 OCIA domain containing 1 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0002083 premature death IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20240523 MGI 1550314 Ociad1 OCIA domain containing 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20220811 MGI 1550314 Ociad1 OCIA domain containing 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0010511 shortened PR interval IEA N RGD:5509061 20231207 MGI 1550314 Ociad1 OCIA domain containing 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0011181 increased hematopoietic cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0011898 abnormal platelet cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0012734 abnormal response to radiation IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0013415 increased myeloid cell number in bone marrow IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0013696 increased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550314 Ociad1 OCIA domain containing 1 gene MP:0013893 decreased common lymphocyte progenitor cell number IAGP N RGD:5509061 20191107 MGI PMID:30952670 1550318 Eipr1 EARP complex and GARP complex interacting protein 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1550318 Eipr1 EARP complex and GARP complex interacting protein 1 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20240919 MGI 1550318 Eipr1 EARP complex and GARP complex interacting protein 1 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20240919 MGI 1550318 Eipr1 EARP complex and GARP complex interacting protein 1 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20240919 MGI 1550318 Eipr1 EARP complex and GARP complex interacting protein 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1550318 Eipr1 EARP complex and GARP complex interacting protein 1 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20240919 MGI 1550318 Eipr1 EARP complex and GARP complex interacting protein 1 gene MP:0009331 absent primitive node IEA N RGD:5509061 20240919 MGI 1550318 Eipr1 EARP complex and GARP complex interacting protein 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1550318 Eipr1 EARP complex and GARP complex interacting protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550318 Eipr1 EARP complex and GARP complex interacting protein 1 gene MP:0012724 absent head fold IEA N RGD:5509061 20240919 MGI 1550318 Eipr1 EARP complex and GARP complex interacting protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1550321 Pcdh12 protocadherin 12 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230601 MGI 1550321 Pcdh12 protocadherin 12 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15541725 1550322 Elmod2 ELMO/CED-12 domain containing 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20200310 MGI 1550322 Elmod2 ELMO/CED-12 domain containing 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1550322 Elmod2 ELMO/CED-12 domain containing 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20200310 MGI 1550322 Elmod2 ELMO/CED-12 domain containing 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 1550322 Elmod2 ELMO/CED-12 domain containing 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20200310 MGI 1550322 Elmod2 ELMO/CED-12 domain containing 2 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20200310 MGI 1550322 Elmod2 ELMO/CED-12 domain containing 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20200310 MGI 1550322 Elmod2 ELMO/CED-12 domain containing 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200310 MGI 1550323 Dcaf10 DDB1 and CUL4 associated factor 10 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1550323 Dcaf10 DDB1 and CUL4 associated factor 10 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20200310 MGI 1550323 Dcaf10 DDB1 and CUL4 associated factor 10 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201231 MGI 1550323 Dcaf10 DDB1 and CUL4 associated factor 10 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20200310 MGI 1550323 Dcaf10 DDB1 and CUL4 associated factor 10 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20210520 MGI 1550323 Dcaf10 DDB1 and CUL4 associated factor 10 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1550327 Adgrf3 adhesion G protein-coupled receptor F3 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38697008 1550330 Taar4 trace amine-associated receptor 4 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:23624375 1550330 Taar4 trace amine-associated receptor 4 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:23624375 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22072671 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210128 MGI PMID:31582721 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:22072671 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20210128 MGI PMID:31582721 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20210128 MGI PMID:31582721 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210128 MGI PMID:31582721 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0001429 dehydration IAGP N RGD:5509061 20210128 MGI PMID:31582721 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:22072671 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:22072671 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22072671 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20210128 MGI PMID:31582721 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22072671 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:22072671 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20210128 MGI PMID:31582721 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:22072671 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:22072671 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:22072671 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20210128 MGI PMID:31582721 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20210128 MGI PMID:31582721 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0008431 abnormal short-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:22072671 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:22072671 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:22072671 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0011396 abnormal sleep behavior IAGP N RGD:5509061 20141003 MGI PMID:22072671 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20210128 MGI PMID:31582721 1550331 Lrrc7 leucine rich repeat containing 7 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22072671 1550332 Ripor2 RHO family interacting cell polarization regulator 2 gene MP:0001967 deafness IAGP N RGD:5509061 20180301 MGI PMID:27269051 1550332 Ripor2 RHO family interacting cell polarization regulator 2 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20180301 MGI PMID:27269051 1550332 Ripor2 RHO family interacting cell polarization regulator 2 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20180301 MGI PMID:27269051 1550332 Ripor2 RHO family interacting cell polarization regulator 2 gene MP:0004525 thin cochlear hair cell stereocilia IAGP N RGD:5509061 20180301 MGI PMID:27269051 1550332 Ripor2 RHO family interacting cell polarization regulator 2 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20180301 MGI PMID:27269051 1550332 Ripor2 RHO family interacting cell polarization regulator 2 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20180301 MGI PMID:27269051 1550332 Ripor2 RHO family interacting cell polarization regulator 2 gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20180301 MGI PMID:27269051 1550332 Ripor2 RHO family interacting cell polarization regulator 2 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20180301 MGI PMID:27269051 1550332 Ripor2 RHO family interacting cell polarization regulator 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20180301 MGI PMID:27269051 1550333 Eif2s2 eukaryotic translation initiation factor 2 subunit 2 beta gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1550333 Eif2s2 eukaryotic translation initiation factor 2 subunit 2 beta gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1550333 Eif2s2 eukaryotic translation initiation factor 2 subunit 2 beta gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1550333 Eif2s2 eukaryotic translation initiation factor 2 subunit 2 beta gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19168544 1550333 Eif2s2 eukaryotic translation initiation factor 2 subunit 2 beta gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:19168544 1550333 Eif2s2 eukaryotic translation initiation factor 2 subunit 2 beta gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19168544 1550333 Eif2s2 eukaryotic translation initiation factor 2 subunit 2 beta gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19168544 1550333 Eif2s2 eukaryotic translation initiation factor 2 subunit 2 beta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550333 Eif2s2 eukaryotic translation initiation factor 2 subunit 2 beta gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1550333 Eif2s2 eukaryotic translation initiation factor 2 subunit 2 beta gene MP:0030934 decreased primordial germ cell proliferation IAGP N RGD:5509061 20190411 MGI PMID:19168544 1550334 Cops3 COP9 signalosome subunit 3 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:12972600 1550334 Cops3 COP9 signalosome subunit 3 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:12972600 1550334 Cops3 COP9 signalosome subunit 3 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:12972600 1550334 Cops3 COP9 signalosome subunit 3 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:12972600 1550334 Cops3 COP9 signalosome subunit 3 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:12972600 1550334 Cops3 COP9 signalosome subunit 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12972600 1550334 Cops3 COP9 signalosome subunit 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12972600 1550334 Cops3 COP9 signalosome subunit 3 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12972600 1550334 Cops3 COP9 signalosome subunit 3 gene MP:0011197 abnormal proamniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:12972600 1550335 Tmem38a transmembrane protein 38A gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20200310 MGI PMID:17611541 1550335 Tmem38a transmembrane protein 38A gene MP:0004085 abnormal heartbeat IAGP N RGD:5509061 20200310 MGI PMID:17611541 1550335 Tmem38a transmembrane protein 38A gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20200310 MGI PMID:17611541 1550335 Tmem38a transmembrane protein 38A gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20200310 MGI PMID:17611541 1550335 Tmem38a transmembrane protein 38A gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:17611541 1550335 Tmem38a transmembrane protein 38A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17611541 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:16757976 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20141003 MGI PMID:16670198 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9875844 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:16670198 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16670198 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:16757976 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16757976 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16757976 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10786799 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9875844 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:17360556 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16757976 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10786799 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10786799 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16670198 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10786799 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10716994 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:16757976 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:17360556 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:17713479 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:19587764 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9875844 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17713479 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:17713479 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:19587764 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10716994 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:10716994 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16670198 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:17360556 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17172844 1550337 Xrcc4 X-ray repair complementing defective repair in Chinese hamster cells 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9875844 1550338 Krt75 keratin 75 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:17851587 1550338 Krt75 keratin 75 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17851587 1550338 Krt75 keratin 75 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:17851587 1550338 Krt75 keratin 75 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:17851587 1550338 Krt75 keratin 75 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:17851587 1550338 Krt75 keratin 75 gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20141003 MGI PMID:17851587 1550338 Krt75 keratin 75 gene MP:0003812 abnormal hair medulla IAGP N RGD:5509061 20141003 MGI PMID:17851587 1550338 Krt75 keratin 75 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1550338 Krt75 keratin 75 gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:17851587 1550340 Arhgap11a Rho GTPase activating protein 11A gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20221201 MGI PMID:33938018 1550340 Arhgap11a Rho GTPase activating protein 11A gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20221201 MGI PMID:33938018 1550340 Arhgap11a Rho GTPase activating protein 11A gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20221201 MGI PMID:33938018 1550340 Arhgap11a Rho GTPase activating protein 11A gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20221201 MGI PMID:33938018 1550340 Arhgap11a Rho GTPase activating protein 11A gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20221201 MGI PMID:33938018 1550340 Arhgap11a Rho GTPase activating protein 11A gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20221201 MGI PMID:33938018 1550340 Arhgap11a Rho GTPase activating protein 11A gene MP:0008947 increased neuron number IAGP N RGD:5509061 20221201 MGI PMID:33938018 1550340 Arhgap11a Rho GTPase activating protein 11A gene MP:0020067 increased neocortex size IAGP N RGD:5509061 20221201 MGI PMID:33938018 1550341 Stk25 serine/threonine kinase 25 (yeast) gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:24225308 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20141003 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0001539 decreased caudal vertebrae number IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0002697 abnormal eye size IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20141003 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20141003 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0009759 abnormal hair follicle bulge morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20160804 MGI 1550342 Pex3 peroxisomal biogenesis factor 3 gene MP:0012725 small sebaceous gland IAGP N RGD:5509061 20150709 MGI PMID:24721909 1550343 Klf9 Kruppel-like transcription factor 9 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200310 MGI 1550343 Klf9 Kruppel-like transcription factor 9 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200310 MGI 1550343 Klf9 Kruppel-like transcription factor 9 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:12640131 1550343 Klf9 Kruppel-like transcription factor 9 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20200310 MGI PMID:12640131 1550345 Trim59 tripartite motif-containing 59 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550345 Trim59 tripartite motif-containing 59 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550345 Trim59 tripartite motif-containing 59 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550345 Trim59 tripartite motif-containing 59 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550345 Trim59 tripartite motif-containing 59 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550345 Trim59 tripartite motif-containing 59 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550345 Trim59 tripartite motif-containing 59 gene MP:0002583 absent extraembryonic ectoderm IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550345 Trim59 tripartite motif-containing 59 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550345 Trim59 tripartite motif-containing 59 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20211021 MGI 1550345 Trim59 tripartite motif-containing 59 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550345 Trim59 tripartite motif-containing 59 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550345 Trim59 tripartite motif-containing 59 gene MP:0005030 absent amnion IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550345 Trim59 tripartite motif-containing 59 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550345 Trim59 tripartite motif-containing 59 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550345 Trim59 tripartite motif-containing 59 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1550345 Trim59 tripartite motif-containing 59 gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550345 Trim59 tripartite motif-containing 59 gene MP:0011209 absent extraembryonic coelom IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550345 Trim59 tripartite motif-containing 59 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1550345 Trim59 tripartite motif-containing 59 gene MP:0012142 absent amniotic cavity IAGP N RGD:5509061 20200310 MGI PMID:29467473 1550347 Frmd6 FERM domain containing 6 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20181227 MGI 1550347 Frmd6 FERM domain containing 6 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1550347 Frmd6 FERM domain containing 6 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1550347 Frmd6 FERM domain containing 6 gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 1550347 Frmd6 FERM domain containing 6 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20181227 MGI 1550347 Frmd6 FERM domain containing 6 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1550347 Frmd6 FERM domain containing 6 gene MP:0005287 narrow eye opening IEA N RGD:5509061 20181227 MGI 1550347 Frmd6 FERM domain containing 6 gene MP:0005655 increased aggression IEA N RGD:5509061 20181227 MGI 1550350 Mrm2 mitochondrial rRNA methyltransferase 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1550350 Mrm2 mitochondrial rRNA methyltransferase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1550350 Mrm2 mitochondrial rRNA methyltransferase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1550350 Mrm2 mitochondrial rRNA methyltransferase 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1550350 Mrm2 mitochondrial rRNA methyltransferase 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1550351 Dnase1l1 deoxyribonuclease 1-like 1 gene MP:0001405 impaired coordination IEA N RGD:5509061 20111116 MGI 1550352 Spmip8 sperm microtubule inner protein 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200310 MGI PMID:19492434 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:19492434 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:19492434 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:12478613 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:19492434 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20200310 MGI PMID:12478613 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200310 MGI PMID:19492434 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:19492434 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20200310 MGI PMID:11468145 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20200310 MGI PMID:19492434 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20200310 MGI PMID:19492434 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0008738 abnormal liver iron level IAGP N RGD:5509061 20200310 MGI PMID:19492434 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20200310 MGI PMID:19492434 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20200310 MGI PMID:19492434 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20200310 MGI PMID:19492434 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:19492434 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12478613 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19492434 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25629408 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10652280 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20200310 MGI PMID:11468145 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1550357 Fth1 ferritin heavy polypeptide 1 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:19492434 1550362 Iah1 isoamyl acetate-hydrolyzing esterase 1 homolog gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 1550362 Iah1 isoamyl acetate-hydrolyzing esterase 1 homolog gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20160421 MGI 1550362 Iah1 isoamyl acetate-hydrolyzing esterase 1 homolog gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20190502 MGI 1550362 Iah1 isoamyl acetate-hydrolyzing esterase 1 homolog gene MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20201001 MGI PMID:32407372 1550362 Iah1 isoamyl acetate-hydrolyzing esterase 1 homolog gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20160421 MGI 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0000274 enlarged heart IAGP N RGD:5509061 20240215 MGI PMID:35700042 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240215 MGI PMID:35700042 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0001265 decreased body size IAGP N RGD:5509061 20240215 MGI PMID:35700042 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0003948 abnormal gas homeostasis IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20240215 MGI PMID:35700042 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0008403 decreased cellular sensitivity to alkylating agents IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0008903 abnormal mesenteric fat pad morphology IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20240215 MGI PMID:35700042 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20240215 MGI PMID:35700042 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20240215 MGI PMID:35700042 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20240215 MGI PMID:35700042 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20240215 MGI PMID:35700042 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20240523 MGI 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0014174 decreased fatty acid beta-oxidation IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0014342 abnormal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240215 MGI PMID:35700042 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0014398 abnormal fat cell mitochondrial morphology IAGP N RGD:5509061 20240718 MGI PMID:22433842 1550363 Oma1 OMA1 zinc metallopeptidase gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20200310 MGI PMID:22433842 1550369 Vps36 vacuolar protein sorting 36 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 1550369 Vps36 vacuolar protein sorting 36 gene MP:0001785 edema IEA N RGD:5509061 20210826 MGI 1550369 Vps36 vacuolar protein sorting 36 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210826 MGI 1550369 Vps36 vacuolar protein sorting 36 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20210826 MGI 1550369 Vps36 vacuolar protein sorting 36 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1550370 Chrd chordin gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0000023 abnormal ear position IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0000023 abnormal ear position IAGP N RGD:5509061 20141003 MGI PMID:19247433 1550370 Chrd chordin gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:19247433 1550370 Chrd chordin gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:19247433 1550370 Chrd chordin gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19247433 1550370 Chrd chordin gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:15013800 1550370 Chrd chordin gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:19247433 1550370 Chrd chordin gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:17634368 1550370 Chrd chordin gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0001086 absent petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0001089 absent nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17634368 1550370 Chrd chordin gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17634368 1550370 Chrd chordin gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17634368 1550370 Chrd chordin gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15013800 1550370 Chrd chordin gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:20508035 1550370 Chrd chordin gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 1550370 Chrd chordin gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:19247433 1550370 Chrd chordin gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0002252 abnormal oropharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0002256 abnormal laryngeal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:19247433 1550370 Chrd chordin gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:19247433 1550370 Chrd chordin gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:17634368 1550370 Chrd chordin gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17634368 1550370 Chrd chordin gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:18789316 1550370 Chrd chordin gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:17634368 1550370 Chrd chordin gene MP:0003499 thyroid gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:18550712 1550370 Chrd chordin gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:20508035 1550370 Chrd chordin gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004387 abnormal prechordal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20508035 1550370 Chrd chordin gene MP:0004422 small temporal bone IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004450 presphenoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004541 absent auditory tube IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004544 absent esophagus IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004549 small trachea IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004554 small pharynx IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0004554 small pharynx IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004572 fusion of basioccipital and basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004592 small mandible IAGP N RGD:5509061 20170921 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15013800 1550370 Chrd chordin gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:18789316 1550370 Chrd chordin gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:18789316 1550370 Chrd chordin gene MP:0004670 small vertebral body IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17634368 1550370 Chrd chordin gene MP:0004899 absent temporal bone squamous part IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004911 absent mandibular condyloid process IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0004913 absent mandibular angle IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:20508035 1550370 Chrd chordin gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0005226 abnormal vertebral arch development IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18789316 1550370 Chrd chordin gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0006285 absent inner ear IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0006288 small otic capsule IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0006290 proboscis IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0006291 aprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0006293 absent nasal placodes IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0006295 absent sclerotome IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0008921 increased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:17634368 1550370 Chrd chordin gene MP:0008926 abnormal anterior definitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:20508035 1550370 Chrd chordin gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:20508035 1550370 Chrd chordin gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0009899 hyoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0010335 fused first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:20508035 1550370 Chrd chordin gene MP:0010657 absent pulmonary trunk IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0010663 abnormal brachiocephalic trunk morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0010729 absent arcus anterior IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17634368 1550370 Chrd chordin gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0011238 abnormal inner ear development IAGP N RGD:5509061 20240822 MGI PMID:10688202 1550370 Chrd chordin gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:10688202 1550370 Chrd chordin gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12810603 1550370 Chrd chordin gene MP:0014517 abnormal outer ear development IAGP N RGD:5509061 20240822 MGI PMID:10688202 1550370 Chrd chordin gene MP:0014517 abnormal outer ear development IAGP N RGD:5509061 20240822 MGI PMID:19247433 1550370 Chrd chordin gene MP:0030375 short zygomatic arch IAGP N RGD:5509061 20171207 MGI PMID:12810603 1550370 Chrd chordin gene MP:0030869 thyroid cartilage hypoplasia IAGP N RGD:5509061 20181101 MGI PMID:12810603 1550370 Chrd chordin gene MP:0030874 cricoid cartilage hypoplasia IAGP N RGD:5509061 20181101 MGI PMID:12810603 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17310981 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20170803 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:12223418 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17310981 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25196150 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:12223418 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0002213 true hermaphroditism IAGP N RGD:5509061 20201224 MGI PMID:17848526 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0002748 abnormal pulmonary valve morphology IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12223418 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:12223418 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20201224 MGI PMID:17848526 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0002996 ovotestis IAGP N RGD:5509061 20201224 MGI PMID:17848526 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0003808 increased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20160304 MGI PMID:25196150 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20160304 MGI PMID:25196150 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0006111 abnormal coronary circulation IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0006123 tricuspid valve atresia IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:17310981 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0009573 abnormal right lung middle lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010224 abnormal heart ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20160304 MGI PMID:25196150 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20160304 MGI PMID:25196150 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010449 heart right ventricle outflow tract stenosis IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010449 heart right ventricle outflow tract stenosis IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010459 supravalvar pulmonary trunk stenosis IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010561 absent coronary vessels IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010640 ventricular myocardium compact layer hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0010824 absent right lung accessory lobe IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160304 MGI PMID:25196150 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411759 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16103912 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20160304 MGI PMID:25196150 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0013602 abnormal Leydig cell differentiation IAGP N RGD:5509061 20150319 MGI PMID:12223418 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0021155 abnormal heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:25196150 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:10892744 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0031525 thin left ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0031529 pulmonary valve hyperplasia IAGP N RGD:5509061 20240118 MGI PMID:10888889 1550372 Zfpm2 zinc finger protein, multitype 2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:25196150 1550375 Rraga Ras-related GTP binding A gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:23263183 1550375 Rraga Ras-related GTP binding A gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20181122 MGI PMID:24768164 1550375 Rraga Ras-related GTP binding A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20181122 MGI PMID:24768164 1550375 Rraga Ras-related GTP binding A gene MP:0000929 open neural tube IAGP N RGD:5509061 20181122 MGI PMID:24768164 1550375 Rraga Ras-related GTP binding A gene MP:0001263 weight loss IAGP N RGD:5509061 20181122 MGI PMID:24768164 1550375 Rraga Ras-related GTP binding A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20181122 MGI PMID:24768164 1550375 Rraga Ras-related GTP binding A gene MP:0002083 premature death IAGP N RGD:5509061 20181122 MGI PMID:24768164 1550375 Rraga Ras-related GTP binding A gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20181122 MGI PMID:24768164 1550375 Rraga Ras-related GTP binding A gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:23263183 1550375 Rraga Ras-related GTP binding A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20181122 MGI PMID:24768164 1550375 Rraga Ras-related GTP binding A gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:23263183 1550375 Rraga Ras-related GTP binding A gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23263183 1550375 Rraga Ras-related GTP binding A gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20181122 MGI PMID:24768164 1550375 Rraga Ras-related GTP binding A gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20181122 MGI PMID:24768164 1550375 Rraga Ras-related GTP binding A gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:23263183 1550375 Rraga Ras-related GTP binding A gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:23263183 1550375 Rraga Ras-related GTP binding A gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23263183 1550375 Rraga Ras-related GTP binding A gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20181122 MGI PMID:24768164 1550375 Rraga Ras-related GTP binding A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23263183 1550375 Rraga Ras-related GTP binding A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20181122 MGI PMID:24768164 1550375 Rraga Ras-related GTP binding A gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20181122 MGI PMID:24768164 1550375 Rraga Ras-related GTP binding A gene MP:0020444 abnormal intestine apoptosis IAGP N RGD:5509061 20181122 MGI PMID:24768164 1550376 Wdr48 WD repeat domain 48 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:24001775 1550376 Wdr48 WD repeat domain 48 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:24001775 1550376 Wdr48 WD repeat domain 48 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:24001775 1550376 Wdr48 WD repeat domain 48 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:24001775 1550376 Wdr48 WD repeat domain 48 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:24001775 1550376 Wdr48 WD repeat domain 48 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20200310 MGI PMID:24001775 1550376 Wdr48 WD repeat domain 48 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:24001775 1550376 Wdr48 WD repeat domain 48 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200310 MGI PMID:24001775 1550376 Wdr48 WD repeat domain 48 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20200310 MGI PMID:24001775 1550376 Wdr48 WD repeat domain 48 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20200310 MGI PMID:24001775 1550376 Wdr48 WD repeat domain 48 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:24001775 1550376 Wdr48 WD repeat domain 48 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20200310 MGI PMID:24001775 1550376 Wdr48 WD repeat domain 48 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24001775 1550376 Wdr48 WD repeat domain 48 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24001775 1550377 Atp13a1 ATPase type 13A1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20210826 MGI 1550377 Atp13a1 ATPase type 13A1 gene MP:0000914 exencephaly IEA N RGD:5509061 20220811 MGI 1550377 Atp13a1 ATPase type 13A1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210826 MGI 1550377 Atp13a1 ATPase type 13A1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210826 MGI 1550377 Atp13a1 ATPase type 13A1 gene MP:0001785 edema IEA N RGD:5509061 20210826 MGI 1550377 Atp13a1 ATPase type 13A1 gene MP:0003717 pallor IEA N RGD:5509061 20210826 MGI 1550377 Atp13a1 ATPase type 13A1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1550377 Atp13a1 ATPase type 13A1 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20210826 MGI 1550377 Atp13a1 ATPase type 13A1 gene MP:0011496 abnormal head size IEA N RGD:5509061 20210826 MGI 1550378 Yap1 yes-associated protein 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21376238 1550378 Yap1 yes-associated protein 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21376238 1550378 Yap1 yes-associated protein 1 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0000524 decreased renal tubule number IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20200310 MGI PMID:20643348 1550378 Yap1 yes-associated protein 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20200310 MGI PMID:26109051 1550378 Yap1 yes-associated protein 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20200310 MGI PMID:20643348 1550378 Yap1 yes-associated protein 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:20643348 1550378 Yap1 yes-associated protein 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20200310 MGI PMID:21376238 1550378 Yap1 yes-associated protein 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20200310 MGI PMID:21376238 1550378 Yap1 yes-associated protein 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:21376238 1550378 Yap1 yes-associated protein 1 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20200310 MGI PMID:21376238 1550378 Yap1 yes-associated protein 1 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20200310 MGI PMID:21376238 1550378 Yap1 yes-associated protein 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20200310 MGI PMID:21376238 1550378 Yap1 yes-associated protein 1 gene MP:0001304 cataract IAGP N RGD:5509061 20210708 MGI PMID:32801350 1550378 Yap1 yes-associated protein 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20210708 MGI PMID:32801350 1550378 Yap1 yes-associated protein 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:18332127 1550378 Yap1 yes-associated protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20200310 MGI PMID:18332127 1550378 Yap1 yes-associated protein 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20200310 MGI PMID:18332127 1550378 Yap1 yes-associated protein 1 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20200310 MGI PMID:21376238 1550378 Yap1 yes-associated protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20200310 MGI PMID:18332127 1550378 Yap1 yes-associated protein 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:18332127 1550378 Yap1 yes-associated protein 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200310 MGI PMID:22028467 1550378 Yap1 yes-associated protein 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20200310 MGI PMID:21376238 1550378 Yap1 yes-associated protein 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20200310 MGI PMID:20643348 1550378 Yap1 yes-associated protein 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20200310 MGI PMID:20643348 1550378 Yap1 yes-associated protein 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:20643348 1550378 Yap1 yes-associated protein 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:26699479 1550378 Yap1 yes-associated protein 1 gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0003046 liver cirrhosis IAGP N RGD:5509061 20200310 MGI PMID:20643348 1550378 Yap1 yes-associated protein 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0003252 abnormal bile duct physiology IAGP N RGD:5509061 20200310 MGI PMID:26109051 1550378 Yap1 yes-associated protein 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20643348 1550378 Yap1 yes-associated protein 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200310 MGI PMID:20643348 1550378 Yap1 yes-associated protein 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200310 MGI PMID:26699479 1550378 Yap1 yes-associated protein 1 gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0003624 anuria IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20210708 MGI PMID:32801350 1550378 Yap1 yes-associated protein 1 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:20643348 1550378 Yap1 yes-associated protein 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:20643348 1550378 Yap1 yes-associated protein 1 gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20200310 MGI PMID:26109051 1550378 Yap1 yes-associated protein 1 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0004755 abnormal loop of Henle morphology IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20200310 MGI PMID:22028467 1550378 Yap1 yes-associated protein 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20200310 MGI PMID:22028467 1550378 Yap1 yes-associated protein 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20200310 MGI PMID:20643348 1550378 Yap1 yes-associated protein 1 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20210708 MGI PMID:32801350 1550378 Yap1 yes-associated protein 1 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20210708 MGI PMID:32801350 1550378 Yap1 yes-associated protein 1 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20210708 MGI PMID:32801350 1550378 Yap1 yes-associated protein 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20200310 MGI PMID:21041407 1550378 Yap1 yes-associated protein 1 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:21041407 1550378 Yap1 yes-associated protein 1 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:21041407 1550378 Yap1 yes-associated protein 1 gene MP:0009392 retina gliosis IAGP N RGD:5509061 20210708 MGI PMID:32801350 1550378 Yap1 yes-associated protein 1 gene MP:0009714 thin epidermis stratum basale IAGP N RGD:5509061 20200310 MGI PMID:21376238 1550378 Yap1 yes-associated protein 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:21041407 1550378 Yap1 yes-associated protein 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20200310 MGI PMID:21041407 1550378 Yap1 yes-associated protein 1 gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20200310 MGI PMID:26109051 1550378 Yap1 yes-associated protein 1 gene MP:0010500 myocardium hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0011004 abnormal epidermal stem cell morphology IAGP N RGD:5509061 20200310 MGI PMID:21376238 1550378 Yap1 yes-associated protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21376238 1550378 Yap1 yes-associated protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23918388 1550378 Yap1 yes-associated protein 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19289085 1550378 Yap1 yes-associated protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22028467 1550378 Yap1 yes-associated protein 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20643348 1550378 Yap1 yes-associated protein 1 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0011364 abnormal metanephros morphology IAGP N RGD:5509061 20200310 MGI PMID:23555292 1550378 Yap1 yes-associated protein 1 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20210708 MGI PMID:32801350 1550378 Yap1 yes-associated protein 1 gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20210708 MGI PMID:32801350 1550378 Yap1 yes-associated protein 1 gene MP:0012236 abnormal cholangiocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:26699479 1550378 Yap1 yes-associated protein 1 gene MP:0012740 abnormal posterior primitive streak morphology IAGP N RGD:5509061 20200310 MGI PMID:16354681 1550378 Yap1 yes-associated protein 1 gene MP:0013611 abnormal bile duct epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:26109051 1550378 Yap1 yes-associated protein 1 gene MP:0020359 abnormal ribbon synapse morphology IAGP N RGD:5509061 20210708 MGI PMID:32801350 1550378 Yap1 yes-associated protein 1 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:20643348 1550380 Creb3l2 cAMP responsive element binding protein 3-like 2 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20200310 MGI PMID:19767744 1550380 Creb3l2 cAMP responsive element binding protein 3-like 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:19767744 1550380 Creb3l2 cAMP responsive element binding protein 3-like 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20200310 MGI PMID:19767744 1550380 Creb3l2 cAMP responsive element binding protein 3-like 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20200310 MGI PMID:19767744 1550380 Creb3l2 cAMP responsive element binding protein 3-like 2 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20200310 MGI PMID:19767744 1550380 Creb3l2 cAMP responsive element binding protein 3-like 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20200310 MGI PMID:19767744 1550380 Creb3l2 cAMP responsive element binding protein 3-like 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20200310 MGI PMID:19767744 1550380 Creb3l2 cAMP responsive element binding protein 3-like 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20200310 MGI PMID:19767744 1550380 Creb3l2 cAMP responsive element binding protein 3-like 2 gene MP:0004733 abnormal thoracic cavity morphology IAGP N RGD:5509061 20200310 MGI PMID:19767744 1550380 Creb3l2 cAMP responsive element binding protein 3-like 2 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20200310 MGI PMID:19767744 1550380 Creb3l2 cAMP responsive element binding protein 3-like 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19767744 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0003960 increased lean body mass IEA N RGD:5509061 20190502 MGI 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0003981 decreased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0004952 increased spleen weight IEA N RGD:5509061 20201022 MGI 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0021133 increased amino acid betaine level IAGP N RGD:5509061 20220721 MGI PMID:21878621 1550381 Bhmt betaine-homocysteine methyltransferase gene MP:0030753 decreased choline level IAGP N RGD:5509061 20180927 MGI PMID:21878621 1550382 Itgal integrin alpha L gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10528208 1550382 Itgal integrin alpha L gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14634125 1550382 Itgal integrin alpha L gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10528208 1550382 Itgal integrin alpha L gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:14634125 1550382 Itgal integrin alpha L gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10528208 1550382 Itgal integrin alpha L gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15955836 1550382 Itgal integrin alpha L gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10224287 1550382 Itgal integrin alpha L gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15955836 1550382 Itgal integrin alpha L gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:8955185 1550382 Itgal integrin alpha L gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:15955836 1550382 Itgal integrin alpha L gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:15955836 1550382 Itgal integrin alpha L gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16872848 1550382 Itgal integrin alpha L gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10224287 1550382 Itgal integrin alpha L gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:20023213 1550382 Itgal integrin alpha L gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:10224287 1550382 Itgal integrin alpha L gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:8955185 1550382 Itgal integrin alpha L gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:19008446 1550382 Itgal integrin alpha L gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230119 MGI 1550382 Itgal integrin alpha L gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:10224287 1550382 Itgal integrin alpha L gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:10528208 1550382 Itgal integrin alpha L gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:20023213 1550382 Itgal integrin alpha L gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12847222 1550382 Itgal integrin alpha L gene MP:0003627 abnormal leukocyte tethering or rolling IAGP N RGD:5509061 20141003 MGI PMID:14634125 1550382 Itgal integrin alpha L gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:10224287 1550382 Itgal integrin alpha L gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:10528208 1550382 Itgal integrin alpha L gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:14634125 1550382 Itgal integrin alpha L gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:15955836 1550382 Itgal integrin alpha L gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:19008446 1550382 Itgal integrin alpha L gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:20023213 1550382 Itgal integrin alpha L gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:8955185 1550382 Itgal integrin alpha L gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10528208 1550382 Itgal integrin alpha L gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10224287 1550382 Itgal integrin alpha L gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15955836 1550382 Itgal integrin alpha L gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20023213 1550382 Itgal integrin alpha L gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10224287 1550382 Itgal integrin alpha L gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:15210787 1550382 Itgal integrin alpha L gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:9637488 1550382 Itgal integrin alpha L gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8955185 1550382 Itgal integrin alpha L gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:15955836 1550382 Itgal integrin alpha L gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15210787 1550382 Itgal integrin alpha L gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230119 MGI 1550382 Itgal integrin alpha L gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20191107 MGI PMID:30194420 1550382 Itgal integrin alpha L gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10224287 1550382 Itgal integrin alpha L gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10224287 1550382 Itgal integrin alpha L gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10224287 1550382 Itgal integrin alpha L gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10224287 1550382 Itgal integrin alpha L gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8955185 1550382 Itgal integrin alpha L gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:12847222 1550382 Itgal integrin alpha L gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:12847222 1550382 Itgal integrin alpha L gene MP:0008599 increased circulating interleukin-2 level IAGP N RGD:5509061 20141003 MGI PMID:12847222 1550382 Itgal integrin alpha L gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12847222 1550382 Itgal integrin alpha L gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:10528208 1550382 Itgal integrin alpha L gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:15955836 1550382 Itgal integrin alpha L gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:19008446 1550382 Itgal integrin alpha L gene MP:0020333 enhanced leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:20023213 1550382 Itgal integrin alpha L gene MP:0030960 abnormal diapedesis IAGP N RGD:5509061 20190725 MGI PMID:20023213 1550384 Tube1 tubulin, epsilon 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20240523 MGI 1550384 Tube1 tubulin, epsilon 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1550384 Tube1 tubulin, epsilon 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20240523 MGI 1550384 Tube1 tubulin, epsilon 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1550384 Tube1 tubulin, epsilon 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20240523 MGI 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:24315444 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20231102 MGI PMID:34587386 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000561 adactyly IAGP N RGD:5509061 20231102 MGI PMID:34587386 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000774 decreased brain size IAGP N RGD:5509061 20231102 MGI PMID:34587386 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20231102 MGI PMID:34587386 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:20614471 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:20614471 1550386 Wls wntless WNT ligand secretion mediator gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24315444 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001428 adipsia IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20231102 MGI PMID:34587386 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:19841259 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:19841259 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001679 thin apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:19841259 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:19841259 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:19841259 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:20614471 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:20614471 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20614471 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:19841259 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20614471 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24315444 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0002861 abnormal tail bud morphology IAGP N RGD:5509061 20231102 MGI PMID:34587386 1550386 Wls wntless WNT ligand secretion mediator gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20231102 MGI PMID:34587386 1550386 Wls wntless WNT ligand secretion mediator gene MP:0003854 abnormal forelimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20231102 MGI PMID:34587386 1550386 Wls wntless WNT ligand secretion mediator gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0004096 abnormal midbrain-hindbrain boundary development IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0004126 thin hypodermis IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0005504 abnormal ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0006101 absent tegmentum IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0006106 absent tectum IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0008052 abnormal serous gland morphology IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20141003 MGI PMID:24315444 1550386 Wls wntless WNT ligand secretion mediator gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:20614471 1550386 Wls wntless WNT ligand secretion mediator gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20231102 MGI PMID:34587386 1550386 Wls wntless WNT ligand secretion mediator gene MP:0009111 pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20614471 1550386 Wls wntless WNT ligand secretion mediator gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0009795 epidermal spongiosis IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20231102 MGI PMID:34587386 1550386 Wls wntless WNT ligand secretion mediator gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0011015 decreased body surface temperature IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20231102 MGI PMID:34587386 1550386 Wls wntless WNT ligand secretion mediator gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19841259 1550386 Wls wntless WNT ligand secretion mediator gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21246653 1550386 Wls wntless WNT ligand secretion mediator gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20614471 1550386 Wls wntless WNT ligand secretion mediator gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:20614471 1550386 Wls wntless WNT ligand secretion mediator gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20141003 MGI PMID:20614471 1550386 Wls wntless WNT ligand secretion mediator gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:20614471 1550386 Wls wntless WNT ligand secretion mediator gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:20614471 1550386 Wls wntless WNT ligand secretion mediator gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0014291 decreased autopod size IAGP N RGD:5509061 20230824 MGI PMID:22377357 1550386 Wls wntless WNT ligand secretion mediator gene MP:0031395 cutaneous mastocytosis IAGP N RGD:5509061 20220721 MGI PMID:23918954 1550386 Wls wntless WNT ligand secretion mediator gene MP:0031395 cutaneous mastocytosis IAGP N RGD:5509061 20220721 MGI PMID:24315444 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210826 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210304 MGI PMID:33483593 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550388 Larp1 La ribonucleoprotein 1, translational regulator gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210826 MGI 1550391 Nup107 nucleoporin 107 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20180426 MGI PMID:29363275 1550392 Hmgn2 high mobility group nucleosomal binding domain 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210422 MGI 1550392 Hmgn2 high mobility group nucleosomal binding domain 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230119 MGI 1550394 Abhd14b abhydrolase domain containing 14b gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1550394 Abhd14b abhydrolase domain containing 14b gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1550396 Kars1 lysyl-tRNA synthetase 1 gene MP:0000745 tremors IEA N RGD:5509061 20231207 MGI 1550396 Kars1 lysyl-tRNA synthetase 1 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20201210 MGI PMID:26091349 1550396 Kars1 lysyl-tRNA synthetase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1550396 Kars1 lysyl-tRNA synthetase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20231207 MGI 1550396 Kars1 lysyl-tRNA synthetase 1 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:26091349 1550397 Nudt2 nudix hydrolase 2 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20240425 MGI PMID:34824277 1550397 Nudt2 nudix hydrolase 2 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20240425 MGI PMID:34824277 1550401 Tll1 tolloid-like gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0000160 kyphosis IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20200310 MGI PMID:12808086 1550401 Tll1 tolloid-like gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20200310 MGI 1550401 Tll1 tolloid-like gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0000299 failure of atrioventricular cushion closure IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20200310 MGI 1550401 Tll1 tolloid-like gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0003109 short femur IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0003717 pallor IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0003755 abnormal palate morphology IEA N RGD:5509061 20200310 MGI 1550401 Tll1 tolloid-like gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0004056 abnormal myocardium compact layer morphology IEA N RGD:5509061 20200310 MGI 1550401 Tll1 tolloid-like gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0004627 abnormal trochanter morphology IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0004675 rib fractures IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0004987 abnormal osteoblast cell number IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20200310 MGI PMID:12808086 1550401 Tll1 tolloid-like gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20200310 MGI PMID:12808086 1550401 Tll1 tolloid-like gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0009445 osteomalacia IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0009868 abnormal descending thoracic aorta morphology IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20200310 MGI 1550401 Tll1 tolloid-like gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20200310 MGI PMID:12808086 1550401 Tll1 tolloid-like gene MP:0010433 double inlet heart left ventricle IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0010924 abnormal osteoid morphology IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0010965 decreased compact bone volume IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12808086 1550401 Tll1 tolloid-like gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10331975 1550401 Tll1 tolloid-like gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0013626 decreased femur yield load IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0013633 decreased femur maximal load IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0013638 decreased femur stiffness IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0013646 decreased energy dissipated prior to femur fracture IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0013941 abnormal enthesis morphology IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0030484 abnormal osteocyte lacuna morphology IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0030487 abnormal osteocyte dendritic process morphology IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550401 Tll1 tolloid-like gene MP:0030827 femur fracture IAGP N RGD:5509061 20200310 MGI PMID:24419319 1550402 Polk polymerase (DNA directed), kappa gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:16731053 1550402 Polk polymerase (DNA directed), kappa gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:12555660 1550403 Uroc1 urocanase domain containing 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1550403 Uroc1 urocanase domain containing 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20200310 MGI 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20240523 MGI 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20210520 MGI PMID:31999954 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20230119 MGI 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230119 MGI 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230119 MGI 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20210520 MGI PMID:31999954 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20230119 MGI 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20230119 MGI 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230119 MGI 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20210520 MGI PMID:31999954 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230119 MGI 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20230601 MGI 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0014384 increased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:31999954 1550408 Eif4g1 eukaryotic translation initiation factor 4, gamma 1 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20210520 MGI PMID:31999954 1550409 Tmem37 transmembrane protein 37 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1550410 Chmp7 charged multivesicular body protein 7 gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20240523 MGI 1550410 Chmp7 charged multivesicular body protein 7 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1550410 Chmp7 charged multivesicular body protein 7 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 1550410 Chmp7 charged multivesicular body protein 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550410 Chmp7 charged multivesicular body protein 7 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0001633 poor circulation IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0002064 seizures IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20211021 MGI 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005283 increased unsaturated fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005284 increased saturated fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005285 decreased unsaturated fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20240523 MGI 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0010360 decreased liver free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0011612 increased circulating ghrelin level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0011939 increased food intake IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0011939 increased food intake IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0011972 decreased circulating lactate dehydrogenase level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0013139 moribund IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20200310 MGI PMID:26479315 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20200310 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:29491146 1550411 Arv1 ARV1 homolog, fatty acid homeostasis modulator gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:29491146 1550413 Rnd2 Rho family GTPase 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1550413 Rnd2 Rho family GTPase 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1550413 Rnd2 Rho family GTPase 2 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 1550413 Rnd2 Rho family GTPase 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1550413 Rnd2 Rho family GTPase 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1550413 Rnd2 Rho family GTPase 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1550413 Rnd2 Rho family GTPase 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20240620 MGI PMID:33596091 1550413 Rnd2 Rho family GTPase 2 gene MP:0001257 increased body length IEA N RGD:5509061 20210128 MGI 1550413 Rnd2 Rho family GTPase 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20240627 MGI PMID:34561615 1550413 Rnd2 Rho family GTPase 2 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210128 MGI 1550413 Rnd2 Rho family GTPase 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1550413 Rnd2 Rho family GTPase 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1550413 Rnd2 Rho family GTPase 2 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210128 MGI 1550413 Rnd2 Rho family GTPase 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20240627 MGI PMID:34561615 1550413 Rnd2 Rho family GTPase 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20240627 MGI PMID:34561615 1550413 Rnd2 Rho family GTPase 2 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20240627 MGI PMID:34561615 1550413 Rnd2 Rho family GTPase 2 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20240627 MGI PMID:34561615 1550413 Rnd2 Rho family GTPase 2 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20221215 MGI 1550413 Rnd2 Rho family GTPase 2 gene MP:0011730 increased myelin sheath thickness IAGP N RGD:5509061 20240620 MGI PMID:33596091 1550413 Rnd2 Rho family GTPase 2 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20240620 MGI PMID:33596091 1550413 Rnd2 Rho family GTPase 2 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210128 MGI 1550413 Rnd2 Rho family GTPase 2 gene MP:0021090 abnormal dendrite arborization pattern IAGP N RGD:5509061 20240627 MGI PMID:34561615 1550415 Slc26a11 solute carrier family 26, member 11 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20240523 MGI 1550415 Slc26a11 solute carrier family 26, member 11 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1550415 Slc26a11 solute carrier family 26, member 11 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:27390771 1550415 Slc26a11 solute carrier family 26, member 11 gene MP:0001406 abnormal gait IEA N RGD:5509061 20240523 MGI 1550415 Slc26a11 solute carrier family 26, member 11 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20200310 MGI PMID:27390771 1550415 Slc26a11 solute carrier family 26, member 11 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20200310 MGI PMID:27390771 1550415 Slc26a11 solute carrier family 26, member 11 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200310 MGI PMID:27390771 1550415 Slc26a11 solute carrier family 26, member 11 gene MP:0012007 abnormal chloride level IAGP N RGD:5509061 20200310 MGI PMID:27390771 1550415 Slc26a11 solute carrier family 26, member 11 gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:27390771 1550418 Parl presenilin associated, rhomboid-like gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0000754 paresis IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0001505 hunched posture IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0001954 respiratory distress IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0002083 premature death IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1550418 Parl presenilin associated, rhomboid-like gene MP:0003103 liver degeneration IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0003354 astrocytosis IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0006051 brainstem hemorrhage IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0008918 microgliosis IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:16839884 1550418 Parl presenilin associated, rhomboid-like gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0013806 encephalopathy IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550418 Parl presenilin associated, rhomboid-like gene MP:0014180 abnormal thymus apoptosis IAGP N RGD:5509061 20190314 MGI PMID:30578322 1550419 Dsg4 desmoglein 4 gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18677469 1550419 Dsg4 desmoglein 4 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18677469 1550419 Dsg4 desmoglein 4 gene MP:0000381 enlarged hair follicles IEA N RGD:5509061 20111116 MGI 1550419 Dsg4 desmoglein 4 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:18677469 1550419 Dsg4 desmoglein 4 gene MP:0000384 distorted hair follicle pattern IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:18677469 1550419 Dsg4 desmoglein 4 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0000580 deformed nails IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0000583 long toenails IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0001190 reddish skin IEA N RGD:5509061 20111116 MGI 1550419 Dsg4 desmoglein 4 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:18677469 1550419 Dsg4 desmoglein 4 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18677469 1550419 Dsg4 desmoglein 4 gene MP:0001279 wavy vibrissae IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:18677469 1550419 Dsg4 desmoglein 4 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:18677469 1550419 Dsg4 desmoglein 4 gene MP:0001786 skin edema IEA N RGD:5509061 20111116 MGI 1550419 Dsg4 desmoglein 4 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18677469 1550419 Dsg4 desmoglein 4 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0003811 abnormal hair cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0003848 brittle hair IEA N RGD:5509061 20111116 MGI 1550419 Dsg4 desmoglein 4 gene MP:0003849 greasy coat IEA N RGD:5509061 20111116 MGI 1550419 Dsg4 desmoglein 4 gene MP:0006365 absent guard hair IEA N RGD:5509061 20111116 MGI 1550419 Dsg4 desmoglein 4 gene MP:0008463 abnormal peripheral lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0010685 abnormal hair follicle inner root sheath morphology IEA N RGD:5509061 20111116 MGI 1550419 Dsg4 desmoglein 4 gene MP:0010688 hair follicle outer root sheath hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8752833 1550419 Dsg4 desmoglein 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20190418 MGI PMID:10839719 1550419 Dsg4 desmoglein 4 gene MP:0013115 focal hair loss in abdominal region IEA N RGD:5509061 20180215 MGI 1550419 Dsg4 desmoglein 4 gene MP:0013116 focal hair loss in head/neck region IEA N RGD:5509061 20180215 MGI 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17001077 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:17001077 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:17001077 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17001077 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17001077 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17170027 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17001077 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:17001077 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:17001077 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:17001077 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17001077 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:17001077 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17001077 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0005628 decreased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:17001077 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0005634 decreased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:17001077 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17001077 1550421 Slc26a3 solute carrier family 26, member 3 gene MP:0014483 increased feces water content IAGP N RGD:5509061 20240704 MGI PMID:17001077 1550423 Drp2 dystrophin related protein 2 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22764250 1550423 Drp2 dystrophin related protein 2 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:22764250 1550423 Drp2 dystrophin related protein 2 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141003 MGI PMID:22764250 1550423 Drp2 dystrophin related protein 2 gene MP:0010742 increased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:22764250 1550428 Crat carnitine acetyltransferase gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22560225 1550428 Crat carnitine acetyltransferase gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:22560225 1550428 Crat carnitine acetyltransferase gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22560225 1550428 Crat carnitine acetyltransferase gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22560225 1550428 Crat carnitine acetyltransferase gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:22560225 1550428 Crat carnitine acetyltransferase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22560225 1550428 Crat carnitine acetyltransferase gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22560225 1550428 Crat carnitine acetyltransferase gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22560225 1550428 Crat carnitine acetyltransferase gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22560225 1550428 Crat carnitine acetyltransferase gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:22560225 1550428 Crat carnitine acetyltransferase gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:22560225 1550428 Crat carnitine acetyltransferase gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20141003 MGI PMID:22560225 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20170105 MGI 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:21989057 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21989057 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:18378701 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:21989057 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18378701 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:18378701 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:21989057 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18378701 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18378701 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18378701 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20211021 MGI 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18378701 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18378701 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:21989057 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18378701 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:18378701 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:21989057 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:21989057 1550432 Arhgef6 Rac/Cdc42 guanine nucleotide exchange factor 6 gene MP:0014471 enhanced B cell migration IAGP N RGD:5509061 20240613 MGI PMID:18378701 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0009929 meningomyelocele IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0012260 encephalomeningocele IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550433 Ptpn9 protein tyrosine phosphatase, non-receptor type 9 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:16330817 1550435 Tln1 talin 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:18086863 1550435 Tln1 talin 1 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:18086863 1550435 Tln1 talin 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20200310 MGI PMID:19793892 1550435 Tln1 talin 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:18086863 1550435 Tln1 talin 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20200310 MGI PMID:19793892 1550435 Tln1 talin 1 gene MP:0002174 abnormal gastrulation movements IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:18188447 1550435 Tln1 talin 1 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:18086863 1550435 Tln1 talin 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:18086863 1550435 Tln1 talin 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200310 MGI PMID:18086863 1550435 Tln1 talin 1 gene MP:0003292 melena IAGP N RGD:5509061 20200310 MGI PMID:18086863 1550435 Tln1 talin 1 gene MP:0003405 abnormal platelet shape IAGP N RGD:5509061 20200310 MGI PMID:18086864 1550435 Tln1 talin 1 gene MP:0003423 reduced thrombolysis IAGP N RGD:5509061 20200310 MGI PMID:20971947 1550435 Tln1 talin 1 gene MP:0003939 abnormal myotome morphology IAGP N RGD:5509061 20200310 MGI PMID:19793892 1550435 Tln1 talin 1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20200310 MGI PMID:19793892 1550435 Tln1 talin 1 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20200310 MGI PMID:19793892 1550435 Tln1 talin 1 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20200310 MGI PMID:18086864 1550435 Tln1 talin 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20200310 MGI PMID:18086863 1550435 Tln1 talin 1 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20200310 MGI PMID:18086864 1550435 Tln1 talin 1 gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20200310 MGI PMID:18086863 1550435 Tln1 talin 1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20200310 MGI PMID:20971947 1550435 Tln1 talin 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20200310 MGI PMID:18086863 1550435 Tln1 talin 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20200310 MGI PMID:18086864 1550435 Tln1 talin 1 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20200310 MGI PMID:18086863 1550435 Tln1 talin 1 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20200310 MGI PMID:18086864 1550435 Tln1 talin 1 gene MP:0006323 abnormal extraembryonic mesoderm development IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20200310 MGI PMID:19793892 1550435 Tln1 talin 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18086863 1550435 Tln1 talin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19793892 1550435 Tln1 talin 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IEA N RGD:5509061 20200310 MGI 1550435 Tln1 talin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0011197 abnormal proamniotic cavity morphology IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0011207 absent ectoplacental cavity IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0011208 small proamniotic cavity IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0011209 absent extraembryonic coelom IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0012104 small amniotic cavity IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20200310 MGI PMID:11084655 1550435 Tln1 talin 1 gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:19793892 1550435 Tln1 talin 1 gene MP:0030959 abnormal myoblast fusion IAGP N RGD:5509061 20200310 MGI PMID:19793892 1550437 Kif5a kinesin family member 5A gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1550437 Kif5a kinesin family member 5A gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23217743 1550437 Kif5a kinesin family member 5A gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:23217743 1550437 Kif5a kinesin family member 5A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23217743 1550437 Kif5a kinesin family member 5A gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:23217743 1550437 Kif5a kinesin family member 5A gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1550437 Kif5a kinesin family member 5A gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20181227 MGI 1550437 Kif5a kinesin family member 5A gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20141003 MGI PMID:21335237 1550437 Kif5a kinesin family member 5A gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23217743 1550437 Kif5a kinesin family member 5A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12682084 1550437 Kif5a kinesin family member 5A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23217743 1550437 Kif5a kinesin family member 5A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550437 Kif5a kinesin family member 5A gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:23217743 1550439 Tubg1 tubulin, gamma 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550439 Tubg1 tubulin, gamma 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550439 Tubg1 tubulin, gamma 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550439 Tubg1 tubulin, gamma 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550439 Tubg1 tubulin, gamma 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1550439 Tubg1 tubulin, gamma 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15893303 1550439 Tubg1 tubulin, gamma 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550439 Tubg1 tubulin, gamma 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550439 Tubg1 tubulin, gamma 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550439 Tubg1 tubulin, gamma 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550439 Tubg1 tubulin, gamma 1 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550439 Tubg1 tubulin, gamma 1 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550439 Tubg1 tubulin, gamma 1 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550439 Tubg1 tubulin, gamma 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550439 Tubg1 tubulin, gamma 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550439 Tubg1 tubulin, gamma 1 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:15893303 1550439 Tubg1 tubulin, gamma 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15893303 1550439 Tubg1 tubulin, gamma 1 gene MP:0020570 decreased premotor cortex size IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550439 Tubg1 tubulin, gamma 1 gene MP:0020596 decreased cerebral cortex total cell area IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550439 Tubg1 tubulin, gamma 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20240418 MGI PMID:31086189 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:16533945 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16533945 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16533944 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16533945 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:21799785 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16533945 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16533945 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21799785 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21799785 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21799785 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16533945 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0002658 abnormal liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:16533945 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16533944 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16533945 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:16533944 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16533944 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:21799785 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:16533945 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:23975099 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:16533944 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0004966 abnormal inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:16533944 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0006205 embryonic lethality between implantation and somite formation IAGP N RGD:5509061 20141003 MGI PMID:21799785 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0008393 absent primordial germ cells IAGP N RGD:5509061 20141003 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21799785 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0009332 abnormal splenocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21799785 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21799785 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:16533945 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20141003 MGI PMID:21799785 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16533944 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16533945 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16533945 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0011411 abnormal gonadal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21799785 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0030934 decreased primordial germ cell proliferation IAGP N RGD:5509061 20190411 MGI PMID:18232736 1550440 Espl1 extra spindle pole bodies 1, separase gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:18232736 1550441 Ifit3 interferon-induced protein with tetratricopeptide repeats 3 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1550441 Ifit3 interferon-induced protein with tetratricopeptide repeats 3 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20220519 MGI 1550441 Ifit3 interferon-induced protein with tetratricopeptide repeats 3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20201022 MGI 1550441 Ifit3 interferon-induced protein with tetratricopeptide repeats 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0000840 abnormal epithalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:8876243 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:8955272 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20141003 MGI PMID:8876243 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:18849985 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15194866 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:8955272 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11160433 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:8876243 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:11493560 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15194866 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:10357931 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:8876243 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:8955272 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:8955272 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0001435 absent suckling reflex IAGP N RGD:5509061 20141003 MGI PMID:8876243 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:8955272 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:8876243 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:8955272 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18849985 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16354917 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150430 MGI PMID:24608965 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11493560 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0003637 cochlear ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11493560 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0003637 cochlear ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8955272 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0003684 abnormal inferior olivary complex morphology IAGP N RGD:5509061 20141003 MGI PMID:8955272 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141225 MGI PMID:24736625 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19323995 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:8876243 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8876243 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8955272 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15194866 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18849985 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0012267 abnormal red nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:8876243 1550443 Pou4f1 POU domain, class 4, transcription factor 1 gene MP:0012268 absent red nucleus IAGP N RGD:5509061 20141003 MGI PMID:8955272 1550444 Gfm2 G elongation factor, mitochondrial 2 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210128 MGI 1550444 Gfm2 G elongation factor, mitochondrial 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550446 Vwa1 von Willebrand factor A domain containing 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20200310 MGI PMID:19279005 1550446 Vwa1 von Willebrand factor A domain containing 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:19279005 1550446 Vwa1 von Willebrand factor A domain containing 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20200310 MGI PMID:19279005 1550447 Tmem106b transmembrane protein 106B gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20210408 MGI PMID:32160553 1550447 Tmem106b transmembrane protein 106B gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20210408 MGI PMID:32160553 1550447 Tmem106b transmembrane protein 106B gene MP:0001258 decreased body length IEA N RGD:5509061 20210520 MGI 1550447 Tmem106b transmembrane protein 106B gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210408 MGI PMID:32160553 1550447 Tmem106b transmembrane protein 106B gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20210408 MGI PMID:32160553 1550447 Tmem106b transmembrane protein 106B gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20210408 MGI PMID:32160553 1550447 Tmem106b transmembrane protein 106B gene MP:0002175 decreased brain weight IEA N RGD:5509061 20220519 MGI 1550447 Tmem106b transmembrane protein 106B gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170105 MGI 1550447 Tmem106b transmembrane protein 106B gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20210408 MGI PMID:32160553 1550447 Tmem106b transmembrane protein 106B gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20170105 MGI 1550447 Tmem106b transmembrane protein 106B gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20170105 MGI 1550447 Tmem106b transmembrane protein 106B gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20210408 MGI PMID:32160553 1550447 Tmem106b transmembrane protein 106B gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20210408 MGI PMID:32160553 1550447 Tmem106b transmembrane protein 106B gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1550447 Tmem106b transmembrane protein 106B gene MP:0010733 abnormal axon initial segment morphology IAGP N RGD:5509061 20210408 MGI PMID:32160553 1550447 Tmem106b transmembrane protein 106B gene MP:0030173 abnormal orbicularis oculi muscle morphology IAGP N RGD:5509061 20210408 MGI PMID:32160553 1550447 Tmem106b transmembrane protein 106B gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20210408 MGI PMID:32160553 1550452 Arhgap20 Rho GTPase activating protein 20 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20220811 MGI 1550454 Dusp13b dual specificity phosphatase 13B gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20231207 MGI 1550455 Synm synemin, intermediate filament protein gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20180830 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0000730 increased satellite cell number IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0000751 myopathy IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20160310 MGI PMID:25567810 1550455 Synm synemin, intermediate filament protein gene MP:0001257 increased body length IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0001260 increased body weight IAGP N RGD:5509061 20180830 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0001399 hyperactivity IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20160114 MGI 1550455 Synm synemin, intermediate filament protein gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20180830 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20160310 MGI PMID:25567810 1550455 Synm synemin, intermediate filament protein gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20160310 MGI PMID:25567810 1550455 Synm synemin, intermediate filament protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20180830 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0002626 increased heart rate IAGP N RGD:5509061 20180830 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20180830 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0002833 increased heart weight IAGP N RGD:5509061 20180830 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20180830 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20180830 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20160310 MGI PMID:25567810 1550455 Synm synemin, intermediate filament protein gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20160310 MGI PMID:25567810 1550455 Synm synemin, intermediate filament protein gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20160310 MGI PMID:25567810 1550455 Synm synemin, intermediate filament protein gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20160310 MGI PMID:25567810 1550455 Synm synemin, intermediate filament protein gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20180830 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0004357 long tibia IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20180830 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20160310 MGI PMID:25567810 1550455 Synm synemin, intermediate filament protein gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20180830 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0009046 muscle twitch IAGP N RGD:5509061 20160310 MGI PMID:25567810 1550455 Synm synemin, intermediate filament protein gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0010240 decreased skeletal muscle size IAGP N RGD:5509061 20160310 MGI PMID:25567810 1550455 Synm synemin, intermediate filament protein gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20180830 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20180830 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20180830 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0013237 abnormal skeletal muscle regeneration IAGP N RGD:5509061 20201217 MGI PMID:25179606 1550455 Synm synemin, intermediate filament protein gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231221 MGI PMID:29247678 1550455 Synm synemin, intermediate filament protein gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:29247678 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20180125 MGI PMID:29036432 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240627 MGI 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20180125 MGI PMID:29036432 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20201231 MGI 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180125 MGI PMID:29036432 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20180125 MGI PMID:29036432 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20180125 MGI PMID:29036432 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20190502 MGI 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20180125 MGI PMID:29036432 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0009850 embryonic lethality between implantation and placentation IAGP N RGD:5509061 20180125 MGI PMID:29036432 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20180125 MGI PMID:29036432 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20190502 MGI 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180125 MGI PMID:29036432 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0014257 embryonic lethality prior to tooth bud stage, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:29036432 1550457 Copb2 COPI coat complex subunit beta 2 gene MP:0020393 increased neuronal precursor proliferation IAGP N RGD:5509061 20180125 MGI PMID:29036432 1550459 Psat1 phosphoserine aminotransferase 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23870131 1550459 Psat1 phosphoserine aminotransferase 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:23870131 1550459 Psat1 phosphoserine aminotransferase 1 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1550459 Psat1 phosphoserine aminotransferase 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23870131 1550459 Psat1 phosphoserine aminotransferase 1 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20160804 MGI 1550459 Psat1 phosphoserine aminotransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:23908115 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23056600 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0000601 small liver IEA N RGD:5509061 20230601 MGI 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23056600 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230601 MGI 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18606138 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18606138 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0002989 small kidney IEA N RGD:5509061 20230601 MGI 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:18606138 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:23908115 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18606138 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:18779865 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:18779865 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:18779865 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23056600 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23056600 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18779865 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23908115 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:23056600 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:23056600 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:18779865 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23908115 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:18779865 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0010924 abnormal osteoid morphology IAGP N RGD:5509061 20141003 MGI PMID:23908115 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20160407 MGI PMID:23908115 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:23908115 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0030439 decreased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:18779865 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:23056600 1550461 Cthrc1 collagen triple helix repeat containing 1 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:23056600 1550462 Nfam1 Nfat activating molecule with ITAM motif 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220519 MGI 1550462 Nfam1 Nfat activating molecule with ITAM motif 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220519 MGI 1550462 Nfam1 Nfat activating molecule with ITAM motif 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220519 MGI 1550462 Nfam1 Nfat activating molecule with ITAM motif 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20220519 MGI 1550462 Nfam1 Nfat activating molecule with ITAM motif 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20220519 MGI 1550464 St8sia3 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20210610 MGI PMID:31455764 1550464 St8sia3 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3 gene MP:0013246 abnormal peptide metabolism IAGP N RGD:5509061 20210610 MGI PMID:31455764 1550465 Fzd6 frizzled class receptor 6 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:16495441 1550465 Fzd6 frizzled class receptor 6 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:15169958 1550465 Fzd6 frizzled class receptor 6 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20180118 MGI PMID:26418459 1550465 Fzd6 frizzled class receptor 6 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20231026 MGI PMID:37622728 1550465 Fzd6 frizzled class receptor 6 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16495441 1550465 Fzd6 frizzled class receptor 6 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:16495441 1550465 Fzd6 frizzled class receptor 6 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20231012 MGI 1550465 Fzd6 frizzled class receptor 6 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:16495441 1550465 Fzd6 frizzled class receptor 6 gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20180118 MGI PMID:26418459 1550465 Fzd6 frizzled class receptor 6 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1550465 Fzd6 frizzled class receptor 6 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16495441 1550465 Fzd6 frizzled class receptor 6 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:16495441 1550465 Fzd6 frizzled class receptor 6 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16495441 1550465 Fzd6 frizzled class receptor 6 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:16495441 1550465 Fzd6 frizzled class receptor 6 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16495441 1550465 Fzd6 frizzled class receptor 6 gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16495441 1550465 Fzd6 frizzled class receptor 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16495441 1550466 Ctnnb1 catenin beta 1 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0000040 absent middle ear ossicles IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0000073 absent craniofacial bones IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0000087 absent mandible IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0000087 absent mandible IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20200310 MGI PMID:19204372 1550466 Ctnnb1 catenin beta 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20200310 MGI PMID:19631205 1550466 Ctnnb1 catenin beta 1 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20200310 MGI PMID:19631205 1550466 Ctnnb1 catenin beta 1 gene MP:0000128 growth retardation of molars IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000128 growth retardation of molars IAGP N RGD:5509061 20200310 MGI PMID:19631205 1550466 Ctnnb1 catenin beta 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20200310 MGI PMID:16854976 1550466 Ctnnb1 catenin beta 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20200310 MGI PMID:16951686 1550466 Ctnnb1 catenin beta 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:15132997 1550466 Ctnnb1 catenin beta 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:16854976 1550466 Ctnnb1 catenin beta 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:21924256 1550466 Ctnnb1 catenin beta 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20200310 MGI PMID:16936073 1550466 Ctnnb1 catenin beta 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:15132997 1550466 Ctnnb1 catenin beta 1 gene MP:0000175 absent bone marrow cell IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:18687666 1550466 Ctnnb1 catenin beta 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:23918954 1550466 Ctnnb1 catenin beta 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:18687666 1550466 Ctnnb1 catenin beta 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0000346 broad head IAGP N RGD:5509061 20200310 MGI PMID:10932191 1550466 Ctnnb1 catenin beta 1 gene MP:0000346 broad head IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:24315444 1550466 Ctnnb1 catenin beta 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:28589954 1550466 Ctnnb1 catenin beta 1 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20200310 MGI PMID:19154719 1550466 Ctnnb1 catenin beta 1 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:24315444 1550466 Ctnnb1 catenin beta 1 gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20200310 MGI PMID:19718027 1550466 Ctnnb1 catenin beta 1 gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20200310 MGI PMID:22412863 1550466 Ctnnb1 catenin beta 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20200310 MGI PMID:24315444 1550466 Ctnnb1 catenin beta 1 gene MP:0000392 accelerated hair follicle regression IAGP N RGD:5509061 20200310 MGI PMID:24315444 1550466 Ctnnb1 catenin beta 1 gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20200310 MGI PMID:20412777 1550466 Ctnnb1 catenin beta 1 gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20200310 MGI PMID:20412777 1550466 Ctnnb1 catenin beta 1 gene MP:0000405 abnormal auchene hair morphology IAGP N RGD:5509061 20200310 MGI PMID:20412777 1550466 Ctnnb1 catenin beta 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20200310 MGI PMID:11371349 1550466 Ctnnb1 catenin beta 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20200310 MGI PMID:22412863 1550466 Ctnnb1 catenin beta 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20200310 MGI PMID:23928991 1550466 Ctnnb1 catenin beta 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20200310 MGI PMID:18652817 1550466 Ctnnb1 catenin beta 1 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0000423 delayed hair regrowth IAGP N RGD:5509061 20200310 MGI PMID:20412777 1550466 Ctnnb1 catenin beta 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200310 MGI PMID:23928991 1550466 Ctnnb1 catenin beta 1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20200310 MGI PMID:19204372 1550466 Ctnnb1 catenin beta 1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20200310 MGI PMID:21228006 1550466 Ctnnb1 catenin beta 1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0000436 abnormal head movements IAGP N RGD:5509061 20200310 MGI PMID:27131348 1550466 Ctnnb1 catenin beta 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20200310 MGI PMID:15132997 1550466 Ctnnb1 catenin beta 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20200310 MGI PMID:15371327 1550466 Ctnnb1 catenin beta 1 gene MP:0000447 flattened snout IAGP N RGD:5509061 20200310 MGI PMID:21228006 1550466 Ctnnb1 catenin beta 1 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20200310 MGI PMID:23873040 1550466 Ctnnb1 catenin beta 1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:15131783 1550466 Ctnnb1 catenin beta 1 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:15131783 1550466 Ctnnb1 catenin beta 1 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:18536716 1550466 Ctnnb1 catenin beta 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20200310 MGI PMID:21205788 1550466 Ctnnb1 catenin beta 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20200310 MGI PMID:18358465 1550466 Ctnnb1 catenin beta 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20200310 MGI PMID:20454682 1550466 Ctnnb1 catenin beta 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20200310 MGI PMID:20454682 1550466 Ctnnb1 catenin beta 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20200310 MGI PMID:22792366 1550466 Ctnnb1 catenin beta 1 gene MP:0000536 hydroureter IAGP N RGD:5509061 20200310 MGI PMID:18358465 1550466 Ctnnb1 catenin beta 1 gene MP:0000536 hydroureter IAGP N RGD:5509061 20200310 MGI PMID:22792366 1550466 Ctnnb1 catenin beta 1 gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20200310 MGI PMID:23928991 1550466 Ctnnb1 catenin beta 1 gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20200310 MGI PMID:20818428 1550466 Ctnnb1 catenin beta 1 gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20200310 MGI PMID:21368895 1550466 Ctnnb1 catenin beta 1 gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20200310 MGI PMID:21504907 1550466 Ctnnb1 catenin beta 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:15132997 1550466 Ctnnb1 catenin beta 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:15371327 1550466 Ctnnb1 catenin beta 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:16854976 1550466 Ctnnb1 catenin beta 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20200310 MGI PMID:12569130 1550466 Ctnnb1 catenin beta 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20200310 MGI PMID:18423204 1550466 Ctnnb1 catenin beta 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20200310 MGI PMID:20152185 1550466 Ctnnb1 catenin beta 1 gene MP:0000553 absent radius IAGP N RGD:5509061 20200310 MGI PMID:23358455 1550466 Ctnnb1 catenin beta 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20200310 MGI PMID:20152185 1550466 Ctnnb1 catenin beta 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20200310 MGI PMID:23358455 1550466 Ctnnb1 catenin beta 1 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20200310 MGI PMID:12569130 1550466 Ctnnb1 catenin beta 1 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20200310 MGI PMID:18423204 1550466 Ctnnb1 catenin beta 1 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20200310 MGI PMID:23358455 1550466 Ctnnb1 catenin beta 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:23358455 1550466 Ctnnb1 catenin beta 1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20200310 MGI PMID:23358455 1550466 Ctnnb1 catenin beta 1 gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20200310 MGI PMID:24290754 1550466 Ctnnb1 catenin beta 1 gene MP:0000653 abnormal sex gland morphology IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0000674 abnormal sweat gland morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20200310 MGI PMID:17652354 1550466 Ctnnb1 catenin beta 1 gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20200310 MGI PMID:28589954 1550466 Ctnnb1 catenin beta 1 gene MP:0000763 abnormal filiform papillae morphology IAGP N RGD:5509061 20200310 MGI PMID:28589954 1550466 Ctnnb1 catenin beta 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:12798297 1550466 Ctnnb1 catenin beta 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:21228006 1550466 Ctnnb1 catenin beta 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20200310 MGI PMID:15219872 1550466 Ctnnb1 catenin beta 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200310 MGI PMID:15219872 1550466 Ctnnb1 catenin beta 1 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20200310 MGI PMID:15219872 1550466 Ctnnb1 catenin beta 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20200310 MGI PMID:15219872 1550466 Ctnnb1 catenin beta 1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0000906 abnormal trigeminal V mesencephalic nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20200310 MGI PMID:22007134 1550466 Ctnnb1 catenin beta 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200310 MGI PMID:22036570 1550466 Ctnnb1 catenin beta 1 gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20200310 MGI PMID:12798297 1550466 Ctnnb1 catenin beta 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0001062 absent oculomotor nerve IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:19237610 1550466 Ctnnb1 catenin beta 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550466 Ctnnb1 catenin beta 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20200310 MGI PMID:19686689 1550466 Ctnnb1 catenin beta 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20200310 MGI PMID:23873040 1550466 Ctnnb1 catenin beta 1 gene MP:0001181 absent lungs IAGP N RGD:5509061 20200310 MGI PMID:19686689 1550466 Ctnnb1 catenin beta 1 gene MP:0001181 absent lungs IAGP N RGD:5509061 20200310 MGI PMID:23873040 1550466 Ctnnb1 catenin beta 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:24315444 1550466 Ctnnb1 catenin beta 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20200310 MGI PMID:19718027 1550466 Ctnnb1 catenin beta 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20200310 MGI PMID:24315444 1550466 Ctnnb1 catenin beta 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:15219872 1550466 Ctnnb1 catenin beta 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:17222338 1550466 Ctnnb1 catenin beta 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:18687666 1550466 Ctnnb1 catenin beta 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:19237610 1550466 Ctnnb1 catenin beta 1 gene MP:0001280 loss of vibrissae IAGP N RGD:5509061 20200310 MGI PMID:18652817 1550466 Ctnnb1 catenin beta 1 gene MP:0001283 sparse vibrissae IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200310 MGI PMID:21228006 1550466 Ctnnb1 catenin beta 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200310 MGI PMID:22007134 1550466 Ctnnb1 catenin beta 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:18652817 1550466 Ctnnb1 catenin beta 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:19570848 1550466 Ctnnb1 catenin beta 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:21228006 1550466 Ctnnb1 catenin beta 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:22007134 1550466 Ctnnb1 catenin beta 1 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20200310 MGI PMID:10932191 1550466 Ctnnb1 catenin beta 1 gene MP:0001304 cataract IAGP N RGD:5509061 20200310 MGI PMID:21228006 1550466 Ctnnb1 catenin beta 1 gene MP:0001306 small lens IAGP N RGD:5509061 20200310 MGI PMID:18652817 1550466 Ctnnb1 catenin beta 1 gene MP:0001337 dry eyes IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0001341 absent eyelids IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200310 MGI PMID:27131348 1550466 Ctnnb1 catenin beta 1 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20200310 MGI PMID:15219872 1550466 Ctnnb1 catenin beta 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20200310 MGI PMID:27131348 1550466 Ctnnb1 catenin beta 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20200310 MGI PMID:12569130 1550466 Ctnnb1 catenin beta 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20200310 MGI PMID:27131348 1550466 Ctnnb1 catenin beta 1 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20200310 MGI PMID:27131348 1550466 Ctnnb1 catenin beta 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:18687666 1550466 Ctnnb1 catenin beta 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:12975353 1550466 Ctnnb1 catenin beta 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:18463637 1550466 Ctnnb1 catenin beta 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20200310 MGI PMID:19023080 1550466 Ctnnb1 catenin beta 1 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20200310 MGI PMID:10662781 1550466 Ctnnb1 catenin beta 1 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20200310 MGI PMID:8582267 1550466 Ctnnb1 catenin beta 1 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20200310 MGI PMID:10662781 1550466 Ctnnb1 catenin beta 1 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20200310 MGI PMID:12569130 1550466 Ctnnb1 catenin beta 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20200310 MGI PMID:10662781 1550466 Ctnnb1 catenin beta 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20200310 MGI PMID:18781635 1550466 Ctnnb1 catenin beta 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20200310 MGI PMID:10662781 1550466 Ctnnb1 catenin beta 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0001684 abnormal axial mesoderm morphology IAGP N RGD:5509061 20200310 MGI PMID:23638095 1550466 Ctnnb1 catenin beta 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20200310 MGI PMID:23638095 1550466 Ctnnb1 catenin beta 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20200310 MGI PMID:10662781 1550466 Ctnnb1 catenin beta 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20200310 MGI PMID:10662781 1550466 Ctnnb1 catenin beta 1 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:10662781 1550466 Ctnnb1 catenin beta 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:8582267 1550466 Ctnnb1 catenin beta 1 gene MP:0001705 abnormal proximal-distal axis patterning IAGP N RGD:5509061 20200310 MGI PMID:10662781 1550466 Ctnnb1 catenin beta 1 gene MP:0001710 absent amniotic folds IAGP N RGD:5509061 20200310 MGI PMID:8582267 1550466 Ctnnb1 catenin beta 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20200310 MGI PMID:12975353 1550466 Ctnnb1 catenin beta 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20200310 MGI PMID:12975353 1550466 Ctnnb1 catenin beta 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20200310 MGI PMID:12975353 1550466 Ctnnb1 catenin beta 1 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550466 Ctnnb1 catenin beta 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550466 Ctnnb1 catenin beta 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20200310 MGI PMID:12975353 1550466 Ctnnb1 catenin beta 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20200310 MGI PMID:17222338 1550466 Ctnnb1 catenin beta 1 gene MP:0001884 mammary gland alveolar hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:24290754 1550466 Ctnnb1 catenin beta 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:12975353 1550466 Ctnnb1 catenin beta 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:19023080 1550466 Ctnnb1 catenin beta 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:15219872 1550466 Ctnnb1 catenin beta 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550466 Ctnnb1 catenin beta 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20200310 MGI PMID:17222338 1550466 Ctnnb1 catenin beta 1 gene MP:0001967 deafness IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0002001 blindness IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:22792366 1550466 Ctnnb1 catenin beta 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:20084116 1550466 Ctnnb1 catenin beta 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20200310 MGI PMID:19631205 1550466 Ctnnb1 catenin beta 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20200310 MGI PMID:22792366 1550466 Ctnnb1 catenin beta 1 gene MP:0002064 seizures IAGP N RGD:5509061 20200310 MGI PMID:15219872 1550466 Ctnnb1 catenin beta 1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20200310 MGI PMID:11371349 1550466 Ctnnb1 catenin beta 1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20200310 MGI PMID:24315444 1550466 Ctnnb1 catenin beta 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20200310 MGI PMID:27134165 1550466 Ctnnb1 catenin beta 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20200310 MGI PMID:22792366 1550466 Ctnnb1 catenin beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:10545105 1550466 Ctnnb1 catenin beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:16951686 1550466 Ctnnb1 catenin beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:17222338 1550466 Ctnnb1 catenin beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:18463637 1550466 Ctnnb1 catenin beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:18536716 1550466 Ctnnb1 catenin beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:18687666 1550466 Ctnnb1 catenin beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19092805 1550466 Ctnnb1 catenin beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19117991 1550466 Ctnnb1 catenin beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:20818428 1550466 Ctnnb1 catenin beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21368895 1550466 Ctnnb1 catenin beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21504907 1550466 Ctnnb1 catenin beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550466 Ctnnb1 catenin beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:23928991 1550466 Ctnnb1 catenin beta 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20200310 MGI PMID:10662781 1550466 Ctnnb1 catenin beta 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:8582267 1550466 Ctnnb1 catenin beta 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200310 MGI PMID:21228006 1550466 Ctnnb1 catenin beta 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20200310 MGI PMID:15132997 1550466 Ctnnb1 catenin beta 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:18463637 1550466 Ctnnb1 catenin beta 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:18358465 1550466 Ctnnb1 catenin beta 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:15729346 1550466 Ctnnb1 catenin beta 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:12798297 1550466 Ctnnb1 catenin beta 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:19204372 1550466 Ctnnb1 catenin beta 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:10545105 1550466 Ctnnb1 catenin beta 1 gene MP:0002188 small heart IAGP N RGD:5509061 20200310 MGI PMID:12975353 1550466 Ctnnb1 catenin beta 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20200310 MGI PMID:15219872 1550466 Ctnnb1 catenin beta 1 gene MP:0002210 abnormal sex determination IAGP N RGD:5509061 20200310 MGI PMID:21490063 1550466 Ctnnb1 catenin beta 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:28196692 1550466 Ctnnb1 catenin beta 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20200310 MGI PMID:19204372 1550466 Ctnnb1 catenin beta 1 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0002351 abnormal cervical lymph node morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:10545105 1550466 Ctnnb1 catenin beta 1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18536716 1550466 Ctnnb1 catenin beta 1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21205788 1550466 Ctnnb1 catenin beta 1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0002579 disorganized secondary lens fibers IAGP N RGD:5509061 20200310 MGI PMID:18652817 1550466 Ctnnb1 catenin beta 1 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:24315444 1550466 Ctnnb1 catenin beta 1 gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20200310 MGI PMID:17222338 1550466 Ctnnb1 catenin beta 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20200310 MGI PMID:19543268 1550466 Ctnnb1 catenin beta 1 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0002726 abnormal pulmonary vein morphology IAGP N RGD:5509061 20200310 MGI PMID:23873040 1550466 Ctnnb1 catenin beta 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:19154719 1550466 Ctnnb1 catenin beta 1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20200310 MGI PMID:27131348 1550466 Ctnnb1 catenin beta 1 gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0002809 increased spinal cord size IAGP N RGD:5509061 20200310 MGI PMID:12798297 1550466 Ctnnb1 catenin beta 1 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:16854976 1550466 Ctnnb1 catenin beta 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20200310 MGI PMID:15219872 1550466 Ctnnb1 catenin beta 1 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20200310 MGI PMID:21262216 1550466 Ctnnb1 catenin beta 1 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20200310 MGI PMID:21924256 1550466 Ctnnb1 catenin beta 1 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20200310 MGI PMID:20010698 1550466 Ctnnb1 catenin beta 1 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19092805 1550466 Ctnnb1 catenin beta 1 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20200310 MGI PMID:18358465 1550466 Ctnnb1 catenin beta 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20200310 MGI PMID:16854976 1550466 Ctnnb1 catenin beta 1 gene MP:0003087 absent allantois IAGP N RGD:5509061 20200310 MGI PMID:8582267 1550466 Ctnnb1 catenin beta 1 gene MP:0003126 abnormal external female genitalia morphology IAGP N RGD:5509061 20200310 MGI PMID:19282366 1550466 Ctnnb1 catenin beta 1 gene MP:0003129 persistent cloaca IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0003153 early eyelid opening IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0003190 fused synovial joints IAGP N RGD:5509061 20200310 MGI PMID:15371327 1550466 Ctnnb1 catenin beta 1 gene MP:0003190 fused synovial joints IAGP N RGD:5509061 20200310 MGI PMID:16936073 1550466 Ctnnb1 catenin beta 1 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550466 Ctnnb1 catenin beta 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:12975353 1550466 Ctnnb1 catenin beta 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20200310 MGI PMID:22007134 1550466 Ctnnb1 catenin beta 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0003236 abnormal lens capsule morphology IAGP N RGD:5509061 20200310 MGI PMID:18652817 1550466 Ctnnb1 catenin beta 1 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:18652817 1550466 Ctnnb1 catenin beta 1 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:19570848 1550466 Ctnnb1 catenin beta 1 gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20200310 MGI PMID:19686689 1550466 Ctnnb1 catenin beta 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20084116 1550466 Ctnnb1 catenin beta 1 gene MP:0003334 pancreas fibrosis IAGP N RGD:5509061 20200310 MGI PMID:17222338 1550466 Ctnnb1 catenin beta 1 gene MP:0003357 impaired granulosa cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550466 Ctnnb1 catenin beta 1 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20200310 MGI PMID:24315444 1550466 Ctnnb1 catenin beta 1 gene MP:0003417 premature endochondral bone ossification IAGP N RGD:5509061 20200310 MGI PMID:16854976 1550466 Ctnnb1 catenin beta 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20200310 MGI PMID:16936073 1550466 Ctnnb1 catenin beta 1 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20200310 MGI PMID:16854976 1550466 Ctnnb1 catenin beta 1 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:22792366 1550466 Ctnnb1 catenin beta 1 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0003456 absent tail IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0003553 abnormal foreskin morphology IAGP N RGD:5509061 20200310 MGI PMID:19282366 1550466 Ctnnb1 catenin beta 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20200310 MGI PMID:20454682 1550466 Ctnnb1 catenin beta 1 gene MP:0003605 fused kidneys IAGP N RGD:5509061 20200310 MGI PMID:22792366 1550466 Ctnnb1 catenin beta 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20200310 MGI PMID:12798297 1550466 Ctnnb1 catenin beta 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:19543268 1550466 Ctnnb1 catenin beta 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:22792366 1550466 Ctnnb1 catenin beta 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20200310 MGI PMID:22377357 1550466 Ctnnb1 catenin beta 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20200310 MGI PMID:16854976 1550466 Ctnnb1 catenin beta 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20200310 MGI PMID:19204372 1550466 Ctnnb1 catenin beta 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20200310 MGI PMID:15866165 1550466 Ctnnb1 catenin beta 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20200310 MGI PMID:21924256 1550466 Ctnnb1 catenin beta 1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20200310 MGI PMID:20412777 1550466 Ctnnb1 catenin beta 1 gene MP:0003826 abnormal Mullerian duct morphology IAGP N RGD:5509061 20200310 MGI PMID:21490063 1550466 Ctnnb1 catenin beta 1 gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20200310 MGI PMID:21924256 1550466 Ctnnb1 catenin beta 1 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20200310 MGI PMID:8582267 1550466 Ctnnb1 catenin beta 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0003895 increased ectoderm apoptosis IAGP N RGD:5509061 20200310 MGI PMID:12569130 1550466 Ctnnb1 catenin beta 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20200310 MGI PMID:23358455 1550466 Ctnnb1 catenin beta 1 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20200310 MGI PMID:12975353 1550466 Ctnnb1 catenin beta 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:18781635 1550466 Ctnnb1 catenin beta 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:23873040 1550466 Ctnnb1 catenin beta 1 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20200310 MGI PMID:15866165 1550466 Ctnnb1 catenin beta 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20200310 MGI PMID:21228006 1550466 Ctnnb1 catenin beta 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20200310 MGI PMID:23638095 1550466 Ctnnb1 catenin beta 1 gene MP:0004081 abnormal globus pallidus morphology IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20200310 MGI PMID:16678101 1550466 Ctnnb1 catenin beta 1 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20200310 MGI PMID:24094324 1550466 Ctnnb1 catenin beta 1 gene MP:0004205 absent hyoid bone IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:23736260 1550466 Ctnnb1 catenin beta 1 gene MP:0004320 split sternum IAGP N RGD:5509061 20200310 MGI PMID:21924256 1550466 Ctnnb1 catenin beta 1 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20200310 MGI PMID:12569130 1550466 Ctnnb1 catenin beta 1 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20200310 MGI PMID:23358455 1550466 Ctnnb1 catenin beta 1 gene MP:0004359 short ulna IAGP N RGD:5509061 20200310 MGI PMID:23358455 1550466 Ctnnb1 catenin beta 1 gene MP:0004382 abnormal hair follicle melanogenesis IAGP N RGD:5509061 20200310 MGI PMID:21862558 1550466 Ctnnb1 catenin beta 1 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20200310 MGI PMID:15870116 1550466 Ctnnb1 catenin beta 1 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20200310 MGI PMID:16738313 1550466 Ctnnb1 catenin beta 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20230629 MGI PMID:34240584 1550466 Ctnnb1 catenin beta 1 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0004539 absent maxilla IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0004539 absent maxilla IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0004572 fusion of basioccipital and basisphenoid bone IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0004672 short ribs IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20200310 MGI PMID:15132997 1550466 Ctnnb1 catenin beta 1 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0004791 absent lower incisors IAGP N RGD:5509061 20200310 MGI PMID:15866165 1550466 Ctnnb1 catenin beta 1 gene MP:0004793 abnormal synaptic vesicle clustering IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20200310 MGI PMID:27131348 1550466 Ctnnb1 catenin beta 1 gene MP:0004830 short incisors IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:28196692 1550466 Ctnnb1 catenin beta 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:18358465 1550466 Ctnnb1 catenin beta 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20200310 MGI PMID:15866165 1550466 Ctnnb1 catenin beta 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20200310 MGI PMID:15866165 1550466 Ctnnb1 catenin beta 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0005077 abnormal melanogenesis IAGP N RGD:5509061 20200310 MGI PMID:22377357 1550466 Ctnnb1 catenin beta 1 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20200310 MGI PMID:12569130 1550466 Ctnnb1 catenin beta 1 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20200310 MGI PMID:23358455 1550466 Ctnnb1 catenin beta 1 gene MP:0005161 hematuria IAGP N RGD:5509061 20200310 MGI PMID:21368895 1550466 Ctnnb1 catenin beta 1 gene MP:0005167 abnormal blood-brain barrier function IAGP N RGD:5509061 20200310 MGI PMID:19023080 1550466 Ctnnb1 catenin beta 1 gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20200310 MGI PMID:21862558 1550466 Ctnnb1 catenin beta 1 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550466 Ctnnb1 catenin beta 1 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550466 Ctnnb1 catenin beta 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20200310 MGI PMID:17222338 1550466 Ctnnb1 catenin beta 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20200310 MGI PMID:10662781 1550466 Ctnnb1 catenin beta 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20200310 MGI PMID:16256739 1550466 Ctnnb1 catenin beta 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20200310 MGI PMID:12798297 1550466 Ctnnb1 catenin beta 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20200310 MGI PMID:12569130 1550466 Ctnnb1 catenin beta 1 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0005315 absent pituitary gland IAGP N RGD:5509061 20200310 MGI PMID:16678101 1550466 Ctnnb1 catenin beta 1 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0005359 growth retardation of incisors IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0005359 growth retardation of incisors IAGP N RGD:5509061 20200310 MGI PMID:19631205 1550466 Ctnnb1 catenin beta 1 gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20200310 MGI PMID:22377357 1550466 Ctnnb1 catenin beta 1 gene MP:0005504 abnormal ligament morphology IAGP N RGD:5509061 20200310 MGI PMID:22377357 1550466 Ctnnb1 catenin beta 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:21571217 1550466 Ctnnb1 catenin beta 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:21924256 1550466 Ctnnb1 catenin beta 1 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20230511 MGI PMID:33497368 1550466 Ctnnb1 catenin beta 1 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20200310 MGI PMID:15866165 1550466 Ctnnb1 catenin beta 1 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20200310 MGI PMID:22036570 1550466 Ctnnb1 catenin beta 1 gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:19023080 1550466 Ctnnb1 catenin beta 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:12975353 1550466 Ctnnb1 catenin beta 1 gene MP:0006236 absent Meibomian glands IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19237610 1550466 Ctnnb1 catenin beta 1 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550466 Ctnnb1 catenin beta 1 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20200310 MGI PMID:24290754 1550466 Ctnnb1 catenin beta 1 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20200310 MGI PMID:16854976 1550466 Ctnnb1 catenin beta 1 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20200310 MGI PMID:20152185 1550466 Ctnnb1 catenin beta 1 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20200310 MGI PMID:22377357 1550466 Ctnnb1 catenin beta 1 gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20200310 MGI PMID:23358455 1550466 Ctnnb1 catenin beta 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22722829 1550466 Ctnnb1 catenin beta 1 gene MP:0006292 abnormal nasal placode morphology IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0006305 abnormal optic eminence morphology IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0006322 abnormal perichondrium morphology IAGP N RGD:5509061 20200310 MGI PMID:16936073 1550466 Ctnnb1 catenin beta 1 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20200310 MGI PMID:28196692 1550466 Ctnnb1 catenin beta 1 gene MP:0006402 small molars IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:18687666 1550466 Ctnnb1 catenin beta 1 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550466 Ctnnb1 catenin beta 1 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20200310 MGI PMID:20084116 1550466 Ctnnb1 catenin beta 1 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20200310 MGI PMID:23202126 1550466 Ctnnb1 catenin beta 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21504907 1550466 Ctnnb1 catenin beta 1 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20200310 MGI PMID:22036570 1550466 Ctnnb1 catenin beta 1 gene MP:0008154 decreased diameter of humerus IAGP N RGD:5509061 20200310 MGI PMID:23358455 1550466 Ctnnb1 catenin beta 1 gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20200310 MGI PMID:15219872 1550466 Ctnnb1 catenin beta 1 gene MP:0008264 absent hippocampus CA1 region IAGP N RGD:5509061 20200310 MGI PMID:15219872 1550466 Ctnnb1 catenin beta 1 gene MP:0008266 absent hippocampus CA2 region IAGP N RGD:5509061 20200310 MGI PMID:15219872 1550466 Ctnnb1 catenin beta 1 gene MP:0008268 absent hippocampus CA3 region IAGP N RGD:5509061 20200310 MGI PMID:15219872 1550466 Ctnnb1 catenin beta 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20200310 MGI PMID:16854976 1550466 Ctnnb1 catenin beta 1 gene MP:0008274 failure of bone ossification IAGP N RGD:5509061 20200310 MGI PMID:16936073 1550466 Ctnnb1 catenin beta 1 gene MP:0008274 failure of bone ossification IAGP N RGD:5509061 20200310 MGI PMID:21924256 1550466 Ctnnb1 catenin beta 1 gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20200310 MGI PMID:16678101 1550466 Ctnnb1 catenin beta 1 gene MP:0008330 absent somatotrophs IAGP N RGD:5509061 20200310 MGI PMID:16678101 1550466 Ctnnb1 catenin beta 1 gene MP:0008333 absent lactotrophs IAGP N RGD:5509061 20200310 MGI PMID:16678101 1550466 Ctnnb1 catenin beta 1 gene MP:0008335 decreased gonadotroph cell number IAGP N RGD:5509061 20200310 MGI PMID:16678101 1550466 Ctnnb1 catenin beta 1 gene MP:0008339 absent thyrotrophs IAGP N RGD:5509061 20200310 MGI PMID:16678101 1550466 Ctnnb1 catenin beta 1 gene MP:0008340 increased corticotroph cell number IAGP N RGD:5509061 20200310 MGI PMID:16678101 1550466 Ctnnb1 catenin beta 1 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20200310 MGI PMID:23918954 1550466 Ctnnb1 catenin beta 1 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20200310 MGI PMID:16854976 1550466 Ctnnb1 catenin beta 1 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20200310 MGI PMID:16854976 1550466 Ctnnb1 catenin beta 1 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0008463 abnormal peripheral lymph node morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0008464 absent peripheral lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0008732 reduced hair shaft melanin granule number IAGP N RGD:5509061 20200310 MGI PMID:21862558 1550466 Ctnnb1 catenin beta 1 gene MP:0008794 increased lens epithelium apoptosis IAGP N RGD:5509061 20200310 MGI PMID:19570848 1550466 Ctnnb1 catenin beta 1 gene MP:0008797 facial cleft IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:12975353 1550466 Ctnnb1 catenin beta 1 gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20200310 MGI PMID:18652817 1550466 Ctnnb1 catenin beta 1 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20200310 MGI PMID:20412777 1550466 Ctnnb1 catenin beta 1 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20200310 MGI PMID:24315444 1550466 Ctnnb1 catenin beta 1 gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20200310 MGI PMID:20412777 1550466 Ctnnb1 catenin beta 1 gene MP:0008860 abnormal hair cycle telogen phase IAGP N RGD:5509061 20200310 MGI PMID:20412777 1550466 Ctnnb1 catenin beta 1 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0009109 decreased pancreas weight IAGP N RGD:5509061 20200310 MGI PMID:17222338 1550466 Ctnnb1 catenin beta 1 gene MP:0009139 failure of Mullerian duct regression IAGP N RGD:5509061 20200310 MGI PMID:21490063 1550466 Ctnnb1 catenin beta 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0009154 pancreatic acinar hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:17222338 1550466 Ctnnb1 catenin beta 1 gene MP:0009199 abnormal external male genitalia morphology IAGP N RGD:5509061 20200310 MGI PMID:19282366 1550466 Ctnnb1 catenin beta 1 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:19117991 1550466 Ctnnb1 catenin beta 1 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20210311 MGI PMID:31819003 1550466 Ctnnb1 catenin beta 1 gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19117991 1550466 Ctnnb1 catenin beta 1 gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20210311 MGI PMID:31819003 1550466 Ctnnb1 catenin beta 1 gene MP:0009272 decreased guard hair length IAGP N RGD:5509061 20200310 MGI PMID:20412777 1550466 Ctnnb1 catenin beta 1 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:27134165 1550466 Ctnnb1 catenin beta 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0009545 abnormal dermis papillary layer morphology IAGP N RGD:5509061 20200310 MGI PMID:24315444 1550466 Ctnnb1 catenin beta 1 gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20818428 1550466 Ctnnb1 catenin beta 1 gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21368895 1550466 Ctnnb1 catenin beta 1 gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:23928991 1550466 Ctnnb1 catenin beta 1 gene MP:0009612 thick epidermis suprabasal layer IAGP N RGD:5509061 20200310 MGI PMID:24315444 1550466 Ctnnb1 catenin beta 1 gene MP:0009629 small brachial lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0009632 small axillary lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0009634 absent popliteal lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0009684 abnormal spinal cord lateral motor column morphology IAGP N RGD:5509061 20200310 MGI PMID:22036570 1550466 Ctnnb1 catenin beta 1 gene MP:0009685 abnormal spinal cord motor column morphology IAGP N RGD:5509061 20200310 MGI PMID:22036570 1550466 Ctnnb1 catenin beta 1 gene MP:0009686 abnormal spinal cord medial motor column morphology IAGP N RGD:5509061 20200310 MGI PMID:22036570 1550466 Ctnnb1 catenin beta 1 gene MP:0009715 thick epidermis stratum basale IAGP N RGD:5509061 20200310 MGI PMID:24315444 1550466 Ctnnb1 catenin beta 1 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20230511 MGI PMID:33497368 1550466 Ctnnb1 catenin beta 1 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20200310 MGI PMID:21862558 1550466 Ctnnb1 catenin beta 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20200310 MGI PMID:19631205 1550466 Ctnnb1 catenin beta 1 gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0009928 abnormal pinna hair pigmentation IAGP N RGD:5509061 20200310 MGI PMID:21862558 1550466 Ctnnb1 catenin beta 1 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20200310 MGI PMID:16951686 1550466 Ctnnb1 catenin beta 1 gene MP:0009933 abnormal tail hair pigmentation IAGP N RGD:5509061 20200310 MGI PMID:21862558 1550466 Ctnnb1 catenin beta 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0010054 increased hepatoblastoma incidence IAGP N RGD:5509061 20200310 MGI PMID:16951686 1550466 Ctnnb1 catenin beta 1 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21205788 1550466 Ctnnb1 catenin beta 1 gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20200310 MGI PMID:18652817 1550466 Ctnnb1 catenin beta 1 gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20200310 MGI PMID:20048081 1550466 Ctnnb1 catenin beta 1 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0010313 increased osteoma incidence IAGP N RGD:5509061 20200310 MGI PMID:15866165 1550466 Ctnnb1 catenin beta 1 gene MP:0010318 increased salivary gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:23736260 1550466 Ctnnb1 catenin beta 1 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:24094324 1550466 Ctnnb1 catenin beta 1 gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19117991 1550466 Ctnnb1 catenin beta 1 gene MP:0010682 abnormal hair follicle infundibulum morphology IAGP N RGD:5509061 20200310 MGI PMID:24315444 1550466 Ctnnb1 catenin beta 1 gene MP:0010741 abnormal melanocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:27134165 1550466 Ctnnb1 catenin beta 1 gene MP:0010864 abnormal enamel knot morphology IAGP N RGD:5509061 20200310 MGI PMID:19631205 1550466 Ctnnb1 catenin beta 1 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0010907 absent lung buds IAGP N RGD:5509061 20200310 MGI PMID:19686689 1550466 Ctnnb1 catenin beta 1 gene MP:0010939 abnormal mandibular prominence morphology IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0010939 abnormal mandibular prominence morphology IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0010964 increased compact bone volume IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15866165 1550466 Ctnnb1 catenin beta 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19543268 1550466 Ctnnb1 catenin beta 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12569130 1550466 Ctnnb1 catenin beta 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15371327 1550466 Ctnnb1 catenin beta 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18358465 1550466 Ctnnb1 catenin beta 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19718027 1550466 Ctnnb1 catenin beta 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22036570 1550466 Ctnnb1 catenin beta 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16854976 1550466 Ctnnb1 catenin beta 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18463637 1550466 Ctnnb1 catenin beta 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20084116 1550466 Ctnnb1 catenin beta 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10662781 1550466 Ctnnb1 catenin beta 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12975353 1550466 Ctnnb1 catenin beta 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19023080 1550466 Ctnnb1 catenin beta 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22036570 1550466 Ctnnb1 catenin beta 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:8582267 1550466 Ctnnb1 catenin beta 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22036570 1550466 Ctnnb1 catenin beta 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18781635 1550466 Ctnnb1 catenin beta 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21228006 1550466 Ctnnb1 catenin beta 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21876000 1550466 Ctnnb1 catenin beta 1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18250098 1550466 Ctnnb1 catenin beta 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15132997 1550466 Ctnnb1 catenin beta 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21228006 1550466 Ctnnb1 catenin beta 1 gene MP:0011194 abnormal hair follicle physiology IAGP N RGD:5509061 20200310 MGI PMID:20412777 1550466 Ctnnb1 catenin beta 1 gene MP:0011195 increased hair follicle apoptosis IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0011195 increased hair follicle apoptosis IAGP N RGD:5509061 20200310 MGI PMID:20412777 1550466 Ctnnb1 catenin beta 1 gene MP:0011195 increased hair follicle apoptosis IAGP N RGD:5509061 20200310 MGI PMID:24315444 1550466 Ctnnb1 catenin beta 1 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20200310 MGI PMID:18358465 1550466 Ctnnb1 catenin beta 1 gene MP:0011298 ureter hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:22792366 1550466 Ctnnb1 catenin beta 1 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20200310 MGI PMID:18358465 1550466 Ctnnb1 catenin beta 1 gene MP:0011407 absent nephrogenic zone IAGP N RGD:5509061 20200310 MGI PMID:18358465 1550466 Ctnnb1 catenin beta 1 gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:18358465 1550466 Ctnnb1 catenin beta 1 gene MP:0011496 abnormal head size IAGP N RGD:5509061 20200310 MGI PMID:21228006 1550466 Ctnnb1 catenin beta 1 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20200310 MGI PMID:12975353 1550466 Ctnnb1 catenin beta 1 gene MP:0011712 arrested osteoblast differentiation IAGP N RGD:5509061 20200310 MGI PMID:16854976 1550466 Ctnnb1 catenin beta 1 gene MP:0011712 arrested osteoblast differentiation IAGP N RGD:5509061 20200310 MGI PMID:16936073 1550466 Ctnnb1 catenin beta 1 gene MP:0011712 arrested osteoblast differentiation IAGP N RGD:5509061 20200310 MGI PMID:21924256 1550466 Ctnnb1 catenin beta 1 gene MP:0011846 decreased kidney collecting duct number IAGP N RGD:5509061 20200310 MGI PMID:18358465 1550466 Ctnnb1 catenin beta 1 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0012110 increased hair follicle number IAGP N RGD:5509061 20200310 MGI PMID:23736260 1550466 Ctnnb1 catenin beta 1 gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0012141 absent hindbrain IAGP N RGD:5509061 20200310 MGI PMID:22190459 1550466 Ctnnb1 catenin beta 1 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0012163 abnormal dental mesenchyme morphology IAGP N RGD:5509061 20200310 MGI PMID:19631205 1550466 Ctnnb1 catenin beta 1 gene MP:0012300 abnormal umbilical cord blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:12975353 1550466 Ctnnb1 catenin beta 1 gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20200310 MGI PMID:27131348 1550466 Ctnnb1 catenin beta 1 gene MP:0012318 slow extinction of fear memory IAGP N RGD:5509061 20200310 MGI PMID:27131348 1550466 Ctnnb1 catenin beta 1 gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19237610 1550466 Ctnnb1 catenin beta 1 gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550466 Ctnnb1 catenin beta 1 gene MP:0012467 increased striatum size IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0012516 absent metencephalon IAGP N RGD:5509061 20200310 MGI PMID:11262227 1550466 Ctnnb1 catenin beta 1 gene MP:0012568 decreased mammary gland tumor incidence in breeding females IAGP N RGD:5509061 20200310 MGI PMID:24290754 1550466 Ctnnb1 catenin beta 1 gene MP:0012570 increased mammary gland tumor incidence in breeding females IAGP N RGD:5509061 20200310 MGI PMID:24290754 1550466 Ctnnb1 catenin beta 1 gene MP:0012571 increased mammary gland tumor incidence in virgin females IAGP N RGD:5509061 20200310 MGI PMID:24290754 1550466 Ctnnb1 catenin beta 1 gene MP:0012739 abnormal anterior primitive streak morphology IAGP N RGD:5509061 20200310 MGI PMID:18781635 1550466 Ctnnb1 catenin beta 1 gene MP:0013180 truncated tail bud IAGP N RGD:5509061 20200310 MGI PMID:22991437 1550466 Ctnnb1 catenin beta 1 gene MP:0013445 Harderian gland atrophy IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0013466 keratoconjunctivitis sicca IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20200310 MGI PMID:15131783 1550466 Ctnnb1 catenin beta 1 gene MP:0013733 squamous metaplasia of bulbourethral gland IAGP N RGD:5509061 20200310 MGI PMID:19117991 1550466 Ctnnb1 catenin beta 1 gene MP:0013734 squamous metaplasia of preputial gland IAGP N RGD:5509061 20200310 MGI PMID:19117991 1550466 Ctnnb1 catenin beta 1 gene MP:0013735 squamous metaplasia of urethral gland IAGP N RGD:5509061 20200310 MGI PMID:19117991 1550466 Ctnnb1 catenin beta 1 gene MP:0013745 abnormal eyelid margin morphology IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0013818 abnormal oral cavity morphology IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0013945 abnormal elbow joint morphology IAGP N RGD:5509061 20200310 MGI PMID:16936073 1550466 Ctnnb1 catenin beta 1 gene MP:0014077 ectopic Paneth cells IAGP N RGD:5509061 20200310 MGI PMID:15131783 1550466 Ctnnb1 catenin beta 1 gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:16936073 1550466 Ctnnb1 catenin beta 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:21860425 1550466 Ctnnb1 catenin beta 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:23736260 1550466 Ctnnb1 catenin beta 1 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:27131348 1550466 Ctnnb1 catenin beta 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:16936073 1550466 Ctnnb1 catenin beta 1 gene MP:0020288 ectopic limbs IAGP N RGD:5509061 20200310 MGI PMID:23358455 1550466 Ctnnb1 catenin beta 1 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20200310 MGI PMID:27131348 1550466 Ctnnb1 catenin beta 1 gene MP:0020526 enlarged thalamus IAGP N RGD:5509061 20200310 MGI PMID:24614104 1550466 Ctnnb1 catenin beta 1 gene MP:0021103 abnormal ventral interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:22036570 1550466 Ctnnb1 catenin beta 1 gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:22036570 1550466 Ctnnb1 catenin beta 1 gene MP:0030252 narrow frontonasal prominence IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0030302 abnormal maxillary zygomatic process morphology IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20200310 MGI PMID:21087601 1550466 Ctnnb1 catenin beta 1 gene MP:0030324 abnormal anterior head development IAGP N RGD:5509061 20200310 MGI PMID:21307168 1550466 Ctnnb1 catenin beta 1 gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20200310 MGI PMID:11585809 1550466 Ctnnb1 catenin beta 1 gene MP:0030906 decreased melanoblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:21862558 1550466 Ctnnb1 catenin beta 1 gene MP:0030908 abnormal melanocyte differentiation IAGP N RGD:5509061 20200310 MGI PMID:27134165 1550466 Ctnnb1 catenin beta 1 gene MP:0031016 decreased granulosa cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550466 Ctnnb1 catenin beta 1 gene MP:0031019 increased granulosa cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21860425 1550466 Ctnnb1 catenin beta 1 gene MP:0031080 pulmonary embolism IAGP N RGD:5509061 20200709 MGI PMID:18687666 1550466 Ctnnb1 catenin beta 1 gene MP:0031395 cutaneous mastocytosis IAGP N RGD:5509061 20220721 MGI PMID:24315444 1550468 Cep97 centrosomal protein 97 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1550468 Cep97 centrosomal protein 97 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1550468 Cep97 centrosomal protein 97 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1550468 Cep97 centrosomal protein 97 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1550468 Cep97 centrosomal protein 97 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1550468 Cep97 centrosomal protein 97 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1550468 Cep97 centrosomal protein 97 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1550468 Cep97 centrosomal protein 97 gene MP:0008854 bleb IEA N RGD:5509061 20210520 MGI 1550468 Cep97 centrosomal protein 97 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550470 Fscn3 fascin actin-bundling protein 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000024 lowered ear position IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000088 short mandible IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20230706 MGI PMID:27606604 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20230706 MGI PMID:27606604 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20230706 MGI PMID:27606604 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001697 abnormal embryo size IAGP N RGD:5509061 20230629 MGI PMID:36449618 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20230629 MGI PMID:36449618 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20230629 MGI PMID:32800293 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0002188 small heart IAGP N RGD:5509061 20230706 MGI PMID:27606604 1550472 Nipbl NIPBL cohesin loading factor gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20230706 MGI PMID:27606604 1550472 Nipbl NIPBL cohesin loading factor gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20230706 MGI PMID:27606604 1550472 Nipbl NIPBL cohesin loading factor gene MP:0003773 eclabion IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20230629 MGI PMID:32800293 1550472 Nipbl NIPBL cohesin loading factor gene MP:0004055 heart atrium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0004351 short humerus IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0004355 short radius IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0004592 small mandible IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20230629 MGI PMID:32800293 1550472 Nipbl NIPBL cohesin loading factor gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20230706 MGI PMID:27606604 1550472 Nipbl NIPBL cohesin loading factor gene MP:0005385 cardiovascular system phenotype IAGP N RGD:5509061 20230706 MGI PMID:27606604 1550472 Nipbl NIPBL cohesin loading factor gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0006411 upturned snout IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0006411 upturned snout IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20230629 MGI PMID:32800293 1550472 Nipbl NIPBL cohesin loading factor gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20230629 MGI PMID:32800293 1550472 Nipbl NIPBL cohesin loading factor gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20230629 MGI PMID:32800293 1550472 Nipbl NIPBL cohesin loading factor gene MP:0008957 abnormal placenta junctional zone morphology IAGP N RGD:5509061 20230629 MGI PMID:32800293 1550472 Nipbl NIPBL cohesin loading factor gene MP:0008958 abnormal trophoblast glycogen cell morphology IAGP N RGD:5509061 20230629 MGI PMID:32800293 1550472 Nipbl NIPBL cohesin loading factor gene MP:0008959 abnormal spongiotrophoblast cell morphology IAGP N RGD:5509061 20230629 MGI PMID:32800293 1550472 Nipbl NIPBL cohesin loading factor gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20230629 MGI PMID:32800293 1550472 Nipbl NIPBL cohesin loading factor gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0009777 abnormal behavioral response to anesthetic IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0010038 abnormal placenta physiology IAGP N RGD:5509061 20230629 MGI PMID:32800293 1550472 Nipbl NIPBL cohesin loading factor gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20230706 MGI PMID:27606604 1550472 Nipbl NIPBL cohesin loading factor gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20230706 MGI PMID:27606604 1550472 Nipbl NIPBL cohesin loading factor gene MP:0010405 ostium secundum atrial septal defect IAGP N RGD:5509061 20230706 MGI PMID:27606604 1550472 Nipbl NIPBL cohesin loading factor gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20230629 MGI PMID:32800293 1550472 Nipbl NIPBL cohesin loading factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20230629 MGI PMID:36449618 1550472 Nipbl NIPBL cohesin loading factor gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20230706 MGI PMID:27606604 1550472 Nipbl NIPBL cohesin loading factor gene MP:0011262 abnormal pharyngeal arch mesenchyme morphology IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20170921 MGI PMID:19763162 1550472 Nipbl NIPBL cohesin loading factor gene MP:0012523 abnormal upper lip morphology IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0012760 decreased cranial neural crest cell proliferation IAGP N RGD:5509061 20151224 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20230629 MGI PMID:32800293 1550472 Nipbl NIPBL cohesin loading factor gene MP:0030065 face hypoplasia IAGP N RGD:5509061 20170921 MGI PMID:24700590 1550472 Nipbl NIPBL cohesin loading factor gene MP:0030303 small ethmoid bone IAGP N RGD:5509061 20171109 MGI PMID:19763162 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20231207 MGI 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20160407 MGI PMID:25088416 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20160407 MGI PMID:25088416 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160407 MGI PMID:25088416 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20160407 MGI PMID:25088416 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20160407 MGI PMID:25088416 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20160407 MGI PMID:25088416 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200514 MGI 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20201022 MGI 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20160407 MGI PMID:25088416 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20160407 MGI PMID:25088416 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20160407 MGI PMID:25088416 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20160407 MGI PMID:25088416 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20160407 MGI PMID:25088416 1550473 Trap1 TNF receptor-associated protein 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20160407 MGI PMID:25088416 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9614081 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210826 MGI 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20170223 MGI PMID:24019477 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20170223 MGI PMID:24019477 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0000646 enlarged adrenocortical cells IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20210826 MGI 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9614081 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:9614081 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20210826 MGI 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210826 MGI 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20231207 MGI 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20170105 MGI 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20210826 MGI 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210826 MGI 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20170223 MGI PMID:24019477 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0012226 increased sterol level IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0012337 increased vitamin D level IAGP N RGD:5509061 20240704 MGI PMID:9614081 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0012338 decreased bile salt level IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0013307 increased adrenal gland weight IAGP N RGD:5509061 20170302 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0014476 abnormal feces lipid level IAGP N RGD:5509061 20240704 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0014479 decreased feces bile salt level IAGP N RGD:5509061 20240704 MGI PMID:11001949 1550475 Cyp27a1 cytochrome P450, family 27, subfamily a, polypeptide 1 gene MP:0031631 decreased lung cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:11001949 1550476 Neurog1 neurogenin 1 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:10640277 1550476 Neurog1 neurogenin 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11825874 1550476 Neurog1 neurogenin 1 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9539122 1550476 Neurog1 neurogenin 1 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9539122 1550476 Neurog1 neurogenin 1 gene MP:0001075 abnormal accessory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9539122 1550476 Neurog1 neurogenin 1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:9539122 1550476 Neurog1 neurogenin 1 gene MP:0001097 abnormal superior glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9539122 1550476 Neurog1 neurogenin 1 gene MP:0001101 abnormal superior vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9539122 1550476 Neurog1 neurogenin 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9539122 1550476 Neurog1 neurogenin 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:10640277 1550476 Neurog1 neurogenin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9539122 1550476 Neurog1 neurogenin 1 gene MP:0013183 absent trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:9539122 1550477 Cpsf1 cleavage and polyadenylation specific factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:21220323 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:9050846 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:9501252 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20200310 MGI PMID:9050846 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:9501252 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:9501252 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20200310 MGI PMID:9501252 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20200310 MGI PMID:21220323 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001396 unidirectional circling IAGP N RGD:5509061 20200310 MGI PMID:9501252 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:9501252 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001399 hyperactivity IAGP N RGD:5509061 20210415 MGI PMID:31907305 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:30682176 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:30682176 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:9501252 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:30682176 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001407 short stride length IAGP N RGD:5509061 20200310 MGI PMID:30682176 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001407 short stride length IAGP N RGD:5509061 20210415 MGI PMID:31907305 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20210415 MGI PMID:31907305 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20200310 MGI PMID:30682176 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001499 abnormal kindling response IAGP N RGD:5509061 20200310 MGI PMID:24700286 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001523 impaired righting response IEA N RGD:5509061 20200310 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20200310 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20200310 MGI PMID:20622165 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001924 infertility IAGP N RGD:5509061 20200310 MGI PMID:9501252 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20200310 MGI PMID:20622165 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200310 MGI PMID:30682176 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:20622165 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:21220323 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:24700286 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:30682176 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:9050846 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:9501252 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20210415 MGI PMID:31907305 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:20622165 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:21220323 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20200310 MGI PMID:9050846 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20200310 MGI PMID:9501252 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20200310 MGI PMID:20622165 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20200310 MGI PMID:24700286 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20200310 MGI PMID:21220323 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0003956 abnormal body size IAGP N RGD:5509061 20200310 MGI PMID:20622165 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:9501252 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:12077185 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20210128 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20200310 MGI PMID:9050846 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20200310 MGI PMID:20622165 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20200310 MGI PMID:31653840 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20210128 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:20622165 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:21220323 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0005407 hyperalgesia IAGP N RGD:5509061 20200310 MGI PMID:9501252 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:12077185 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:21220323 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:21220323 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20200310 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20201022 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20200310 MGI PMID:19225179 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20200310 MGI PMID:20622165 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:30682176 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20210128 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0010769 abnormal survival IAGP N RGD:5509061 20200310 MGI PMID:20622165 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0010769 abnormal survival IAGP N RGD:5509061 20200310 MGI PMID:21220323 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24700286 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24700286 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9050846 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:30682176 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9050846 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9501252 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19225179 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0011678 abnormal vomeronasal sensory neuron physiology IAGP N RGD:5509061 20200310 MGI PMID:31653840 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20210415 MGI PMID:31907305 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20200310 MGI 1550478 Gnao1 guanine nucleotide binding protein, alpha O gene MP:0020424 increased kindling response IAGP N RGD:5509061 20200310 MGI PMID:30682176 1550484 Krt10 keratin 10 gene MP:0000020 scaly ears IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0000410 waved hair IEA N RGD:5509061 20111116 MGI 1550484 Krt10 keratin 10 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20180719 MGI PMID:15679119 1550484 Krt10 keratin 10 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20180719 MGI PMID:15679119 1550484 Krt10 keratin 10 gene MP:0001190 reddish skin IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0001192 scaly skin IAGP N RGD:5509061 20180719 MGI PMID:11157989 1550484 Krt10 keratin 10 gene MP:0001192 scaly skin IAGP N RGD:5509061 20180719 MGI PMID:24751727 1550484 Krt10 keratin 10 gene MP:0001192 scaly skin IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0001195 flaky skin IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0001201 translucent skin IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0001208 blistering IAGP N RGD:5509061 20180719 MGI PMID:11157989 1550484 Krt10 keratin 10 gene MP:0001208 blistering IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0001212 skin lesions IAGP N RGD:5509061 20180719 MGI PMID:11157989 1550484 Krt10 keratin 10 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20180719 MGI PMID:11408568 1550484 Krt10 keratin 10 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20180719 MGI PMID:15482487 1550484 Krt10 keratin 10 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20180719 MGI PMID:22375063 1550484 Krt10 keratin 10 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20180719 MGI PMID:24751727 1550484 Krt10 keratin 10 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20180719 MGI PMID:15482487 1550484 Krt10 keratin 10 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20180719 MGI PMID:22375063 1550484 Krt10 keratin 10 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20180719 MGI PMID:24751727 1550484 Krt10 keratin 10 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20180719 MGI PMID:11157989 1550484 Krt10 keratin 10 gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20180719 MGI PMID:11408568 1550484 Krt10 keratin 10 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20180719 MGI PMID:11408568 1550484 Krt10 keratin 10 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20180719 MGI PMID:15679119 1550484 Krt10 keratin 10 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20180719 MGI PMID:11157989 1550484 Krt10 keratin 10 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20180719 MGI PMID:22375063 1550484 Krt10 keratin 10 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20180719 MGI PMID:24751727 1550484 Krt10 keratin 10 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0001874 acanthosis IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20180719 MGI PMID:15482487 1550484 Krt10 keratin 10 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0002992 abnormal sebaceous lipid secretion IAGP N RGD:5509061 20180719 MGI PMID:15679119 1550484 Krt10 keratin 10 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20180719 MGI PMID:22375063 1550484 Krt10 keratin 10 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0003849 greasy coat IAGP N RGD:5509061 20180719 MGI PMID:15679119 1550484 Krt10 keratin 10 gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20180719 MGI PMID:22375063 1550484 Krt10 keratin 10 gene MP:0009596 abnormal stratum corneum lipid matrix formation IAGP N RGD:5509061 20180719 MGI PMID:15679119 1550484 Krt10 keratin 10 gene MP:0009600 hypergranulosis IAGP N RGD:5509061 20180719 MGI PMID:24751727 1550484 Krt10 keratin 10 gene MP:0009606 increased keratohyalin granule size IAGP N RGD:5509061 20180719 MGI PMID:11408568 1550484 Krt10 keratin 10 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:11157989 1550484 Krt10 keratin 10 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:22375063 1550484 Krt10 keratin 10 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:8603923 1550484 Krt10 keratin 10 gene MP:0013373 increased sebum secretion IAGP N RGD:5509061 20180719 MGI PMID:15679119 1550484 Krt10 keratin 10 gene MP:0013375 abnormal sebocyte morphology IAGP N RGD:5509061 20180719 MGI PMID:15679119 1550484 Krt10 keratin 10 gene MP:0013376 abnormal sebocyte differentiation IAGP N RGD:5509061 20180719 MGI PMID:15679119 1550484 Krt10 keratin 10 gene MP:0014056 increased sebocyte proliferation IAGP N RGD:5509061 20180719 MGI PMID:15679119 1550485 Iigp1 interferon inducible GTPase 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20200310 MGI PMID:16304607 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20170105 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:9382868 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20170105 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:9382868 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:11150240 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9382868 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9382868 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0002608 increased hematocrit IEA N RGD:5509061 20170105 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9382868 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20210520 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20170105 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0003870 decreased urine glucose level IEA N RGD:5509061 20211021 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:9382868 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210520 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20181227 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:9585413 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:9382868 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20170105 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20211021 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0011471 decreased urine creatinine level IEA N RGD:5509061 20210128 MGI 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:9382868 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:9382868 1550486 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19050047 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220519 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17671657 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:19050047 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220519 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220519 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19050047 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:19050047 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20220519 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0003357 impaired granulosa cell differentiation IAGP N RGD:5509061 20220519 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0003657 abnormal erythrocyte osmotic lysis IAGP N RGD:5509061 20141003 MGI PMID:19050047 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20220519 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21124450 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19050047 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20220519 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:19050047 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:19050047 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17671657 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20141003 MGI PMID:21124450 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20220519 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:19050047 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0011124 increased primary ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0011128 increased tertiary ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20220519 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0014514 increased circulating anti-Mullerian hormone level IAGP N RGD:5509061 20240822 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0021106 abnormal secondary ovarian follicle morphology IAGP N RGD:5509061 20220519 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:35459945 1550489 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:14573616 1550491 Cbx7 chromobox 7 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:22214847 1550491 Cbx7 chromobox 7 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:22214847 1550491 Cbx7 chromobox 7 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22214847 1550491 Cbx7 chromobox 7 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22214847 1550491 Cbx7 chromobox 7 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20150326 MGI PMID:22214847 1550491 Cbx7 chromobox 7 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:22214847 1550491 Cbx7 chromobox 7 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22214847 1550491 Cbx7 chromobox 7 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22214847 1550491 Cbx7 chromobox 7 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22214847 1550491 Cbx7 chromobox 7 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22214847 1550491 Cbx7 chromobox 7 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22214847 1550491 Cbx7 chromobox 7 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22214847 1550491 Cbx7 chromobox 7 gene MP:0012725 small sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:23870131 1550492 Trim54 tripartite motif-containing 54 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200310 MGI PMID:17360532 1550492 Trim54 tripartite motif-containing 54 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:17360532 1550492 Trim54 tripartite motif-containing 54 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:17360532 1550492 Trim54 tripartite motif-containing 54 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:17360532 1550492 Trim54 tripartite motif-containing 54 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:17360532 1550492 Trim54 tripartite motif-containing 54 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:17360532 1550492 Trim54 tripartite motif-containing 54 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:17360532 1550492 Trim54 tripartite motif-containing 54 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20200310 MGI PMID:17360532 1550492 Trim54 tripartite motif-containing 54 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20200310 MGI PMID:17360532 1550492 Trim54 tripartite motif-containing 54 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20200310 MGI PMID:17360532 1550492 Trim54 tripartite motif-containing 54 gene MP:0005202 lethargy IAGP N RGD:5509061 20200310 MGI PMID:17360532 1550492 Trim54 tripartite motif-containing 54 gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231221 MGI PMID:17360532 1550496 Adam28 a disintegrin and metallopeptidase domain 28 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20210114 MGI PMID:30647853 1550496 Adam28 a disintegrin and metallopeptidase domain 28 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20210114 MGI PMID:30647853 1550496 Adam28 a disintegrin and metallopeptidase domain 28 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20210114 MGI PMID:30647853 1550496 Adam28 a disintegrin and metallopeptidase domain 28 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210114 MGI PMID:30647853 1550496 Adam28 a disintegrin and metallopeptidase domain 28 gene MP:0012762 abnormal alpha-beta T cell morphology IAGP N RGD:5509061 20210114 MGI PMID:30647853 1550498 Brinp3 bone morphogenetic protein/retinoic acid inducible neural specific 3 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20230601 MGI 1550498 Brinp3 bone morphogenetic protein/retinoic acid inducible neural specific 3 gene MP:0000154 rib fusion IEA N RGD:5509061 20230601 MGI 1550498 Brinp3 bone morphogenetic protein/retinoic acid inducible neural specific 3 gene MP:0000162 lordosis IEA N RGD:5509061 20230601 MGI 1550498 Brinp3 bone morphogenetic protein/retinoic acid inducible neural specific 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1550498 Brinp3 bone morphogenetic protein/retinoic acid inducible neural specific 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1550498 Brinp3 bone morphogenetic protein/retinoic acid inducible neural specific 3 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20230601 MGI 1550498 Brinp3 bone morphogenetic protein/retinoic acid inducible neural specific 3 gene MP:0001262 decreased body weight IEA N RGD:5509061 20240523 MGI 1550498 Brinp3 bone morphogenetic protein/retinoic acid inducible neural specific 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1550498 Brinp3 bone morphogenetic protein/retinoic acid inducible neural specific 3 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20230601 MGI 1550498 Brinp3 bone morphogenetic protein/retinoic acid inducible neural specific 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1550499 Usp11 ubiquitin specific peptidase 11 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20210128 MGI 1550499 Usp11 ubiquitin specific peptidase 11 gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20191024 MGI PMID:30733438 1550499 Usp11 ubiquitin specific peptidase 11 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20191024 MGI PMID:30733438 1550499 Usp11 ubiquitin specific peptidase 11 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1550499 Usp11 ubiquitin specific peptidase 11 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20191024 MGI PMID:30733438 1550499 Usp11 ubiquitin specific peptidase 11 gene MP:0004958 enlarged prostate gland IAGP N RGD:5509061 20191024 MGI PMID:30733438 1550499 Usp11 ubiquitin specific peptidase 11 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1550499 Usp11 ubiquitin specific peptidase 11 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20191024 MGI PMID:30733438 1550499 Usp11 ubiquitin specific peptidase 11 gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20191024 MGI PMID:30733438 1550499 Usp11 ubiquitin specific peptidase 11 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20191024 MGI PMID:30733438 1550499 Usp11 ubiquitin specific peptidase 11 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20191024 MGI PMID:30733438 1550503 Angpt2 angiopoietin 2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20200310 MGI PMID:12361603 1550503 Angpt2 angiopoietin 2 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20200310 MGI PMID:12361603 1550503 Angpt2 angiopoietin 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1550503 Angpt2 angiopoietin 2 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1550503 Angpt2 angiopoietin 2 gene MP:0000706 small thymus IEA N RGD:5509061 20210128 MGI 1550503 Angpt2 angiopoietin 2 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20210128 MGI 1550503 Angpt2 angiopoietin 2 gene MP:0001201 translucent skin IAGP N RGD:5509061 20200310 MGI PMID:12361603 1550503 Angpt2 angiopoietin 2 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20200310 MGI PMID:12361603 1550503 Angpt2 angiopoietin 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20200310 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0001786 skin edema IAGP N RGD:5509061 20200310 MGI PMID:12361603 1550503 Angpt2 angiopoietin 2 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:12361603 1550503 Angpt2 angiopoietin 2 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200310 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1550503 Angpt2 angiopoietin 2 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:12361603 1550503 Angpt2 angiopoietin 2 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20200310 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0004226 absent Schlemm's canal IAGP N RGD:5509061 20200310 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20200310 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20200310 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0005257 abnormal intraocular pressure IAGP N RGD:5509061 20200310 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0005324 ascites IAGP N RGD:5509061 20200310 MGI PMID:12361603 1550503 Angpt2 angiopoietin 2 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20230810 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20200310 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20200310 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20200310 MGI PMID:12361603 1550503 Angpt2 angiopoietin 2 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20200310 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200310 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200310 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20200310 MGI PMID:12361603 1550503 Angpt2 angiopoietin 2 gene MP:0009274 buphthalmos IAGP N RGD:5509061 20200310 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12361603 1550503 Angpt2 angiopoietin 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1550503 Angpt2 angiopoietin 2 gene MP:0012080 chylous ascites IAGP N RGD:5509061 20200310 MGI PMID:12361603 1550503 Angpt2 angiopoietin 2 gene MP:0012684 abnormal pleural cavity morphology IAGP N RGD:5509061 20200310 MGI PMID:12361603 1550503 Angpt2 angiopoietin 2 gene MP:0031213 increased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:25202984 1550503 Angpt2 angiopoietin 2 gene MP:0031500 increased cornea size IAGP N RGD:5509061 20230810 MGI PMID:25202984 1550506 Wdr59 WD repeat domain 59 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210128 MGI 1550506 Wdr59 WD repeat domain 59 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20200402 MGI 1550506 Wdr59 WD repeat domain 59 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200310 MGI 1550506 Wdr59 WD repeat domain 59 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20210826 MGI 1550506 Wdr59 WD repeat domain 59 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1550506 Wdr59 WD repeat domain 59 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20231207 MGI 1550506 Wdr59 WD repeat domain 59 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1550506 Wdr59 WD repeat domain 59 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550506 Wdr59 WD repeat domain 59 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1550507 Hspa4l heat shock protein 4 like gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20200310 MGI PMID:16923965 1550507 Hspa4l heat shock protein 4 like gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20200310 MGI PMID:16923965 1550507 Hspa4l heat shock protein 4 like gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20200310 MGI PMID:16923965 1550507 Hspa4l heat shock protein 4 like gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:16923965 1550507 Hspa4l heat shock protein 4 like gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:16923965 1550507 Hspa4l heat shock protein 4 like gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:16923965 1550507 Hspa4l heat shock protein 4 like gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20200310 MGI PMID:16923965 1550507 Hspa4l heat shock protein 4 like gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:16923965 1550507 Hspa4l heat shock protein 4 like gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:16923965 1550507 Hspa4l heat shock protein 4 like gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20200310 MGI PMID:16923965 1550507 Hspa4l heat shock protein 4 like gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20200310 MGI PMID:16923965 1550507 Hspa4l heat shock protein 4 like gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20200310 MGI PMID:16923965 1550507 Hspa4l heat shock protein 4 like gene MP:0005633 increased circulating sodium level IAGP N RGD:5509061 20200310 MGI PMID:16923965 1550507 Hspa4l heat shock protein 4 like gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:16923965 1550507 Hspa4l heat shock protein 4 like gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20200310 MGI PMID:16923965 1550508 Pkp2 plakophilin 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200310 MGI PMID:15479741 1550508 Pkp2 plakophilin 2 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:15479741 1550508 Pkp2 plakophilin 2 gene MP:0001633 poor circulation IAGP N RGD:5509061 20200310 MGI PMID:15479741 1550508 Pkp2 plakophilin 2 gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:15479741 1550508 Pkp2 plakophilin 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20200310 MGI PMID:15479741 1550508 Pkp2 plakophilin 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20200310 MGI PMID:15479741 1550508 Pkp2 plakophilin 2 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20200310 MGI PMID:15479741 1550508 Pkp2 plakophilin 2 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20200310 MGI PMID:15479741 1550508 Pkp2 plakophilin 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20200310 MGI PMID:15479741 1550508 Pkp2 plakophilin 2 gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20200310 MGI PMID:15479741 1550508 Pkp2 plakophilin 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15479741 1550508 Pkp2 plakophilin 2 gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:15479741 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20200310 MGI 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001190 reddish skin IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001192 scaly skin IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001195 flaky skin IEA N RGD:5509061 20200310 MGI 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001208 blistering IAGP N RGD:5509061 20200310 MGI PMID:15466487 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001212 skin lesions IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:15590704 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001230 epidermal desquamation IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001230 epidermal desquamation IAGP N RGD:5509061 20200806 MGI PMID:31255470 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20200310 MGI PMID:15466487 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20200310 MGI PMID:15466487 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20200310 MGI PMID:20703245 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20200806 MGI PMID:31255470 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20200310 MGI PMID:15590704 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001283 sparse vibrissae IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001429 dehydration IAGP N RGD:5509061 20200310 MGI PMID:15466487 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001429 dehydration IAGP N RGD:5509061 20200310 MGI PMID:15590704 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001429 dehydration IAGP N RGD:5509061 20200310 MGI PMID:20703245 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001874 acanthosis IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001874 acanthosis IAGP N RGD:5509061 20200310 MGI PMID:20703245 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20200806 MGI PMID:31255470 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20200310 MGI PMID:20703245 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20200806 MGI PMID:31255470 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20200310 MGI PMID:20703245 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20200806 MGI PMID:31255470 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20200310 MGI PMID:15466487 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20200310 MGI PMID:15590704 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20200806 MGI PMID:31255470 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20200806 MGI PMID:31255470 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20200310 MGI PMID:15590704 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15466487 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15590704 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15619623 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20703245 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200806 MGI PMID:31255470 1550511 Spink5 serine peptidase inhibitor, Kazal type 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1550512 Isca1 iron-sulfur cluster assembly 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1550512 Isca1 iron-sulfur cluster assembly 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1550512 Isca1 iron-sulfur cluster assembly 1 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191205 MGI 1550512 Isca1 iron-sulfur cluster assembly 1 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1550512 Isca1 iron-sulfur cluster assembly 1 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191205 MGI 1550512 Isca1 iron-sulfur cluster assembly 1 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1550512 Isca1 iron-sulfur cluster assembly 1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20170105 MGI 1550512 Isca1 iron-sulfur cluster assembly 1 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191205 MGI 1550512 Isca1 iron-sulfur cluster assembly 1 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191205 MGI 1550512 Isca1 iron-sulfur cluster assembly 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1550512 Isca1 iron-sulfur cluster assembly 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550512 Isca1 iron-sulfur cluster assembly 1 gene MP:0012724 absent head fold IEA N RGD:5509061 20191205 MGI 1550512 Isca1 iron-sulfur cluster assembly 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191205 MGI 1550512 Isca1 iron-sulfur cluster assembly 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1550513 Fbxl22 F-box and leucine-rich repeat protein 22 gene MP:0002764 short tibia IEA N RGD:5509061 20200310 MGI 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:19109567 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20200310 MGI PMID:19109567 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:16914726 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:19109567 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0002415 abnormal neutrophil differentiation IAGP N RGD:5509061 20200310 MGI PMID:19109567 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200310 MGI PMID:21727190 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20200310 MGI PMID:21727190 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20200310 MGI PMID:19109567 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20200310 MGI PMID:16914726 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:21727190 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:21727190 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20200310 MGI PMID:21727190 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:16914726 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20200310 MGI PMID:21727190 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20200310 MGI PMID:16914726 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:21727190 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:19109567 1550514 Vtcn1 V-set domain containing T cell activation inhibitor 1 gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20200310 MGI PMID:21727190 1550515 Slc16a13 solute carrier family 16 (monocarboxylic acid transporters), member 13 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20211209 MGI PMID:34211098 1550515 Slc16a13 solute carrier family 16 (monocarboxylic acid transporters), member 13 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20211209 MGI PMID:34211098 1550515 Slc16a13 solute carrier family 16 (monocarboxylic acid transporters), member 13 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20211209 MGI PMID:34211098 1550515 Slc16a13 solute carrier family 16 (monocarboxylic acid transporters), member 13 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20211209 MGI PMID:34211098 1550515 Slc16a13 solute carrier family 16 (monocarboxylic acid transporters), member 13 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20211209 MGI PMID:34211098 1550515 Slc16a13 solute carrier family 16 (monocarboxylic acid transporters), member 13 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20211209 MGI PMID:34211098 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0003415 priapism IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0008283 small hippocampus IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0008918 microgliosis IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550516 Scyl2 SCY1-like 2 (S. cerevisiae) gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20200310 MGI PMID:26203146 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210826 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:17543860 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17543860 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19211677 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20181227 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20181227 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19509342 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17543860 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19211677 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17543860 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19211677 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19509342 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0002626 increased heart rate IEA N RGD:5509061 20210128 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:17543860 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:19211677 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20181227 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23348741 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:23348741 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:17543860 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:19211677 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19211677 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:17543860 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20210826 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:19211677 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:17543860 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:19211677 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23318132 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:24413433 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20150226 MGI PMID:24589552 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20181227 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:23348741 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17543860 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17543860 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:19211677 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20181227 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0009268 absent cerebellum fissure IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20150226 MGI PMID:24589552 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20161208 MGI PMID:17543860 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19509342 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0010008 abnormal Purkinje cell migration IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19509342 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20170302 MGI PMID:26035387 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20181227 MGI 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23348741 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0013507 increased ovary apoptosis IAGP N RGD:5509061 20161208 MGI PMID:17543860 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20161208 MGI PMID:17543860 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0030024 abnormal meiotic attachment of telomere to nuclear envelope IAGP N RGD:5509061 20170803 MGI PMID:24413433 1550518 Sun1 Sad1 and UNC84 domain containing 1 gene MP:0030024 abnormal meiotic attachment of telomere to nuclear envelope IAGP N RGD:5509061 20191024 MGI PMID:30718482 1550519 Spg21 SPG21, maspardin gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20210318 MGI PMID:20661613 1550519 Spg21 SPG21, maspardin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210318 MGI PMID:20661613 1550519 Spg21 SPG21, maspardin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210318 MGI PMID:26978163 1550519 Spg21 SPG21, maspardin gene MP:0001513 limb grasping IAGP N RGD:5509061 20210318 MGI PMID:26978163 1550519 Spg21 SPG21, maspardin gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20210318 MGI PMID:20661613 1550519 Spg21 SPG21, maspardin gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20210318 MGI PMID:26978163 1550519 Spg21 SPG21, maspardin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20210318 MGI PMID:26978163 1550519 Spg21 SPG21, maspardin gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20210318 MGI PMID:26978163 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200820 MGI PMID:31645418 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:16878172 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20210128 MGI PMID:33097186 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20200709 MGI PMID:32485164 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20200625 MGI PMID:32485164 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20200820 MGI PMID:32725927 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20200820 MGI PMID:32725927 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20171116 MGI PMID:17499227 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:12075344 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20171116 MGI PMID:17499227 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20171116 MGI PMID:17499227 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20210128 MGI PMID:33097186 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200416 MGI PMID:16001071 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200416 MGI PMID:24800825 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200416 MGI PMID:27019629 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200820 MGI PMID:31645418 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20200625 MGI PMID:32485164 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12075344 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20200625 MGI PMID:32485164 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200820 MGI PMID:31645418 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:16505206 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20171116 MGI PMID:17499227 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20171116 MGI PMID:17499227 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:16505206 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20200416 MGI PMID:16001071 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0003136 yellow coat color IEA N RGD:5509061 20170323 MGI 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16505206 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0003184 increased angiotensin I-converting enzyme activity IAGP N RGD:5509061 20200416 MGI PMID:27019629 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0003288 intestinal edema IAGP N RGD:5509061 20210128 MGI PMID:33097186 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0003292 melena IAGP N RGD:5509061 20210128 MGI PMID:33097186 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20200820 MGI PMID:29570986 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20171116 MGI PMID:17499227 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20210128 MGI PMID:33097186 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20171116 MGI PMID:17499227 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20200416 MGI PMID:16001071 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20200416 MGI PMID:24800825 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20210128 MGI PMID:33097186 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0004013 decreased pulmonary artery pressure IAGP N RGD:5509061 20200820 MGI PMID:29570986 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0005036 diarrhea IAGP N RGD:5509061 20160331 MGI PMID:25448263 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12075344 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20171116 MGI PMID:17499227 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20200416 MGI PMID:16001071 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20200416 MGI PMID:16001071 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16878172 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20200820 MGI PMID:32725927 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20200416 MGI PMID:27019629 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200416 MGI PMID:27019629 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16505206 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20171116 MGI PMID:17499227 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16505206 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:16505206 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20200820 MGI PMID:32725927 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:16505206 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20171116 MGI PMID:17499227 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16878172 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20171116 MGI PMID:17499227 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20160331 MGI PMID:25448263 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20210128 MGI PMID:33097186 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20200625 MGI PMID:32485164 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0008629 increased circulating interleukin-9 level IAGP N RGD:5509061 20200625 MGI PMID:32485164 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20171116 MGI PMID:17499227 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20230601 MGI 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16505206 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200820 MGI PMID:31645418 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:16505206 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20210128 MGI PMID:33097186 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20160331 MGI PMID:25448263 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20200820 MGI PMID:31645418 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20210128 MGI PMID:33097186 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20200625 MGI PMID:32485164 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0011044 increased lung elastance IAGP N RGD:5509061 20200416 MGI PMID:16001071 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20171116 MGI PMID:17499227 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0012041 increased susceptibility to pulmonary hyaline membrane formation IAGP N RGD:5509061 20200416 MGI PMID:16001071 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0012041 increased susceptibility to pulmonary hyaline membrane formation IAGP N RGD:5509061 20200416 MGI PMID:24800825 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160331 MGI PMID:25448263 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20210128 MGI PMID:33097186 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20200416 MGI PMID:16001071 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0020446 increased NAD(P)H oxidase activity IAGP N RGD:5509061 20171116 MGI PMID:17499227 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0020861 abnormal cornea wound healing IAGP N RGD:5509061 20200820 MGI PMID:32725927 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:24800825 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200625 MGI PMID:32485164 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16007097 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:12075344 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:24800825 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0031228 decreased angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:16001071 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0031229 increased angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:16001071 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0031229 increased angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:16505206 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0031229 increased angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:16878172 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0031231 decreased circulating angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:16001071 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0031232 increased circulating angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:16001071 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0031232 increased circulating angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:16505206 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0031232 increased circulating angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:16878172 1550521 Ace2 angiotensin converting enzyme 2 gene MP:0031319 impaired intestine regeneration IAGP N RGD:5509061 20211125 MGI PMID:33097186 1550522 Guca2a guanylate cyclase activator 2a (guanylin) gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1550522 Guca2a guanylate cyclase activator 2a (guanylin) gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1550522 Guca2a guanylate cyclase activator 2a (guanylin) gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:12466132 1550522 Guca2a guanylate cyclase activator 2a (guanylin) gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:12466132 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20160630 MGI PMID:26888934 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160630 MGI PMID:26888934 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0002626 increased heart rate IEA N RGD:5509061 20210128 MGI 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20240523 MGI 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20160630 MGI PMID:26888934 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20201022 MGI 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20201022 MGI 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20160630 MGI PMID:26888934 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20160630 MGI PMID:26888934 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20160630 MGI PMID:26888934 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0010511 shortened PR interval IEA N RGD:5509061 20210128 MGI 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0010571 shortened ST segment IEA N RGD:5509061 20210128 MGI 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160630 MGI PMID:26888934 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0011954 shortened PQ interval IEA N RGD:5509061 20210128 MGI 1550523 Sorbs2 sorbin and SH3 domain containing 2 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:26888934 1550524 Rps6kc1 ribosomal protein S6 kinase polypeptide 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1550524 Rps6kc1 ribosomal protein S6 kinase polypeptide 1 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20240523 MGI 1550524 Rps6kc1 ribosomal protein S6 kinase polypeptide 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1550525 Meis1 Meis homeobox 1 gene MP:0000239 absent common myeloid progenitor cells IAGP N RGD:5509061 20141003 MGI PMID:15882575 1550525 Meis1 Meis homeobox 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15882575 1550525 Meis1 Meis homeobox 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20151022 MGI PMID:25363539 1550525 Meis1 Meis homeobox 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1550525 Meis1 Meis homeobox 1 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1550525 Meis1 Meis homeobox 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20240801 MGI PMID:38314840 1550525 Meis1 Meis homeobox 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15882575 1550525 Meis1 Meis homeobox 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15882575 1550525 Meis1 Meis homeobox 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15882575 1550525 Meis1 Meis homeobox 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20151022 MGI PMID:25363539 1550525 Meis1 Meis homeobox 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22995899 1550525 Meis1 Meis homeobox 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15882575 1550525 Meis1 Meis homeobox 1 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22995899 1550525 Meis1 Meis homeobox 1 gene MP:0003714 absent platelets IAGP N RGD:5509061 20141003 MGI PMID:15882575 1550525 Meis1 Meis homeobox 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:15882575 1550525 Meis1 Meis homeobox 1 gene MP:0003717 pallor IAGP N RGD:5509061 20151022 MGI PMID:25363539 1550525 Meis1 Meis homeobox 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22995899 1550525 Meis1 Meis homeobox 1 gene MP:0008253 absent megakaryocytes IAGP N RGD:5509061 20141003 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0008253 absent megakaryocytes IAGP N RGD:5509061 20151022 MGI PMID:25363539 1550525 Meis1 Meis homeobox 1 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22995899 1550525 Meis1 Meis homeobox 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20201022 MGI 1550525 Meis1 Meis homeobox 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1550525 Meis1 Meis homeobox 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20151022 MGI PMID:25363539 1550525 Meis1 Meis homeobox 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22995899 1550525 Meis1 Meis homeobox 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15882575 1550525 Meis1 Meis homeobox 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550525 Meis1 Meis homeobox 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15882575 1550525 Meis1 Meis homeobox 1 gene MP:0020327 abnormal capillary branching pattern IAGP N RGD:5509061 20160714 MGI PMID:14713950 1550525 Meis1 Meis homeobox 1 gene MP:0020478 abnormal circadian sleep/wake cycle IAGP N RGD:5509061 20240801 MGI PMID:38314840 1550525 Meis1 Meis homeobox 1 gene MP:0021198 abnormal sleep duration IAGP N RGD:5509061 20240801 MGI PMID:38314840 1550527 Skic2 SKI2 subunit of superkiller complex gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20230720 MGI 1550527 Skic2 SKI2 subunit of superkiller complex gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20230720 MGI 1550527 Skic2 SKI2 subunit of superkiller complex gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20111116 MGI 1550527 Skic2 SKI2 subunit of superkiller complex gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230720 MGI 1550527 Skic2 SKI2 subunit of superkiller complex gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230720 MGI 1550529 Hyal1 hyaluronoglucosaminidase 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18344557 1550529 Hyal1 hyaluronoglucosaminidase 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18344557 1550529 Hyal1 hyaluronoglucosaminidase 1 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:18344557 1550529 Hyal1 hyaluronoglucosaminidase 1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:18344557 1550529 Hyal1 hyaluronoglucosaminidase 1 gene MP:0014429 increased hyaluronic acid level IAGP N RGD:5509061 20240425 MGI PMID:18344557 1550532 Ttll4 tubulin tyrosine ligase-like family, member 4 gene MP:0001262 decreased body weight IEA N RGD:5509061 20200310 MGI 1550532 Ttll4 tubulin tyrosine ligase-like family, member 4 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20200310 MGI 1550532 Ttll4 tubulin tyrosine ligase-like family, member 4 gene MP:0001413 abnormal response to new environment IEA N RGD:5509061 20200310 MGI 1550532 Ttll4 tubulin tyrosine ligase-like family, member 4 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20200310 MGI 1550533 Katna1 katanin p60 (ATPase-containing) subunit A1 gene MP:0001148 enlarged testis IEA N RGD:5509061 20200514 MGI 1550533 Katna1 katanin p60 (ATPase-containing) subunit A1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20200514 MGI 1550533 Katna1 katanin p60 (ATPase-containing) subunit A1 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20200514 MGI 1550533 Katna1 katanin p60 (ATPase-containing) subunit A1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200409 MGI PMID:31685876 1550533 Katna1 katanin p60 (ATPase-containing) subunit A1 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20200409 MGI PMID:31685876 1550533 Katna1 katanin p60 (ATPase-containing) subunit A1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200409 MGI PMID:31685876 1550533 Katna1 katanin p60 (ATPase-containing) subunit A1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1550533 Katna1 katanin p60 (ATPase-containing) subunit A1 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20200409 MGI PMID:31685876 1550533 Katna1 katanin p60 (ATPase-containing) subunit A1 gene MP:0030981 abnormal dentate gyrus subgranular zone morphology IAGP N RGD:5509061 20200409 MGI PMID:31685876 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20200310 MGI PMID:26609154 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200514 MGI 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20200514 MGI 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200514 MGI 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20200310 MGI PMID:17329413 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0001967 deafness IAGP N RGD:5509061 20200310 MGI PMID:26609154 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20200310 MGI PMID:26609154 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200514 MGI 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0003896 prolonged PR interval IEA N RGD:5509061 20210520 MGI 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:26609154 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:26609154 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20200310 MGI PMID:26609154 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:26609154 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20200310 MGI PMID:26609154 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20200310 MGI PMID:26609154 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0004528 fused outer hair cell stereocilia IAGP N RGD:5509061 20200310 MGI PMID:26609154 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0004597 increased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20200310 MGI PMID:26609154 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0004628 Deiters cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:26609154 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20200310 MGI PMID:26609154 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0004749 nonsyndromic hearing loss IAGP N RGD:5509061 20200310 MGI PMID:26609154 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200514 MGI 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200514 MGI 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:17329413 1550534 Usp53 ubiquitin specific peptidase 53 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:26609154 1550536 Gdf6 growth differentiation factor 6 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0001262 decreased body weight IEA N RGD:5509061 20111116 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0001732 postnatal growth retardation IEA N RGD:5509061 20111116 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20230601 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0001963 abnormal hearing physiology IEA N RGD:5509061 20111116 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0002082 postnatal lethality IEA N RGD:5509061 20111116 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230601 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230601 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0004602 abnormal vertebral articular process morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0005110 absent talus IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0005508 abnormal skeleton morphology IEA N RGD:5509061 20111116 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20111116 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0008372 small malleus IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0008919 fused tarsal bones IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230601 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0011047 increased lung tissue damping IEA N RGD:5509061 20230601 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1550536 Gdf6 growth differentiation factor 6 gene MP:0030106 small incus IAGP N RGD:5509061 20170928 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0030108 abnormal incudostapedial joint morphology IAGP N RGD:5509061 20170928 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0030109 abnormal incudomalleolar joint morphology IAGP N RGD:5509061 20170928 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0030123 small middle ear ossicles IAGP N RGD:5509061 20170928 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0030127 small stapes IAGP N RGD:5509061 20170928 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0030349 absent coronal suture IAGP N RGD:5509061 20171116 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0030400 abnormal stapes annular ligament morphology IAGP N RGD:5509061 20171207 MGI PMID:12606286 1550536 Gdf6 growth differentiation factor 6 gene MP:0030401 absent stapes annular ligament IAGP N RGD:5509061 20171207 MGI PMID:12606286 1550537 Psd pleckstrin and Sec7 domain containing gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1550537 Psd pleckstrin and Sec7 domain containing gene MP:0000692 small spleen IEA N RGD:5509061 20210128 MGI 1550537 Psd pleckstrin and Sec7 domain containing gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1550542 Vwa5a von Willebrand factor A domain containing 5A gene MP:0001314 cornea opacity IEA N RGD:5509061 20200402 MGI 1550542 Vwa5a von Willebrand factor A domain containing 5A gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1550542 Vwa5a von Willebrand factor A domain containing 5A gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20240523 MGI 1550543 Slc16a3 solute carrier family 16 (monocarboxylic acid transporters), member 3 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20201029 MGI PMID:31837519 1550543 Slc16a3 solute carrier family 16 (monocarboxylic acid transporters), member 3 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20201210 MGI PMID:32693190 1550543 Slc16a3 solute carrier family 16 (monocarboxylic acid transporters), member 3 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20201029 MGI PMID:31837519 1550543 Slc16a3 solute carrier family 16 (monocarboxylic acid transporters), member 3 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20201029 MGI PMID:31837519 1550543 Slc16a3 solute carrier family 16 (monocarboxylic acid transporters), member 3 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20201029 MGI PMID:31837519 1550543 Slc16a3 solute carrier family 16 (monocarboxylic acid transporters), member 3 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20201210 MGI PMID:32693190 1550543 Slc16a3 solute carrier family 16 (monocarboxylic acid transporters), member 3 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:32693190 1550544 Cgrrf1 cell growth regulator with ring finger domain 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1550544 Cgrrf1 cell growth regulator with ring finger domain 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20200402 MGI 1550544 Cgrrf1 cell growth regulator with ring finger domain 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1550544 Cgrrf1 cell growth regulator with ring finger domain 1 gene MP:0008346 increased gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 1550544 Cgrrf1 cell growth regulator with ring finger domain 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1550544 Cgrrf1 cell growth regulator with ring finger domain 1 gene MP:0013421 increased CD5-positive gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 1550545 Usp29 ubiquitin specific peptidase 29 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1550545 Usp29 ubiquitin specific peptidase 29 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1550545 Usp29 ubiquitin specific peptidase 29 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20181220 MGI PMID:27327533 1550545 Usp29 ubiquitin specific peptidase 29 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1550545 Usp29 ubiquitin specific peptidase 29 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20181220 MGI PMID:27327533 1550545 Usp29 ubiquitin specific peptidase 29 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1550545 Usp29 ubiquitin specific peptidase 29 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20181220 MGI PMID:27327533 1550545 Usp29 ubiquitin specific peptidase 29 gene MP:0010723 paternal effect IAGP N RGD:5509061 20181220 MGI PMID:27327533 1550547 Tspyl4 TSPY-like 4 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20220811 MGI 1550547 Tspyl4 TSPY-like 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1550547 Tspyl4 TSPY-like 4 gene MP:0001513 limb grasping IEA N RGD:5509061 20220811 MGI 1550547 Tspyl4 TSPY-like 4 gene MP:0005655 increased aggression IEA N RGD:5509061 20220811 MGI 1550548 Rnf139 ring finger protein 139 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200310 MGI PMID:26319415 1550548 Rnf139 ring finger protein 139 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200310 MGI PMID:26319415 1550548 Rnf139 ring finger protein 139 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:26319415 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:17611414 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:17611414 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:15755804 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:17611414 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0003891 increased allantois apoptosis IAGP N RGD:5509061 20200310 MGI PMID:17611414 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:17611414 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20200310 MGI PMID:17611414 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0004559 small allantois IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0006386 absent somites IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20200310 MGI PMID:17611414 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20200310 MGI PMID:17611414 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15755804 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17611414 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20200310 MGI PMID:17611414 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0012183 decreased paraxial mesoderm size IAGP N RGD:5509061 20200310 MGI PMID:15755804 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0012183 decreased paraxial mesoderm size IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0012184 absent paraxial mesoderm IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:17611414 1550550 Ddx11 DEAD/H box helicase 11 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:22678773 1550552 Septin2 septin 2 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20240523 MGI 1550552 Septin2 septin 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1550552 Septin2 septin 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1550552 Septin2 septin 2 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1550552 Septin2 septin 2 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20230914 MGI PMID:36378242 1550552 Septin2 septin 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1550552 Septin2 septin 2 gene MP:0005386 behavior/neurological phenotype IAGP N RGD:5509061 20230914 MGI PMID:36378242 1550552 Septin2 septin 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1550552 Septin2 septin 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1550552 Septin2 septin 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1550553 Otub2 OTU domain, ubiquitin aldehyde binding 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20240606 MGI PMID:36288705 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20190912 MGI PMID:26252542 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0001177 atelectasis IAGP N RGD:5509061 20190912 MGI PMID:26252542 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0001575 cyanosis IAGP N RGD:5509061 20190912 MGI PMID:26252542 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0001953 respiratory failure IAGP N RGD:5509061 20190912 MGI PMID:26252542 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0001954 respiratory distress IAGP N RGD:5509061 20190912 MGI PMID:26252542 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20190912 MGI PMID:26252542 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20190912 MGI PMID:26252542 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20190912 MGI PMID:26252542 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0004781 abnormal surfactant composition IAGP N RGD:5509061 20190912 MGI PMID:26252542 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20190912 MGI PMID:26252542 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0009908 protruding tongue IEA N RGD:5509061 20210520 MGI 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0010890 decreased alveolar lamellar body number IAGP N RGD:5509061 20190912 MGI PMID:26252542 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0010898 abnormal pulmonary alveolus epithelium morphology IAGP N RGD:5509061 20190912 MGI PMID:26252542 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0010903 abnormal pulmonary alveolus wall morphology IAGP N RGD:5509061 20190912 MGI PMID:26252542 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20190912 MGI PMID:26252542 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:26252542 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550555 Rcn3 reticulocalbin 3, EF-hand calcium binding domain gene MP:0031006 increased lung glycogen level IAGP N RGD:5509061 20200130 MGI PMID:26252542 1550557 Spata4 spermatogenesis associated 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1550559 Rttn rotatin gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210826 MGI 1550559 Rttn rotatin gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 1550559 Rttn rotatin gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 1550559 Rttn rotatin gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20111116 MGI 1550559 Rttn rotatin gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:11900971 1550559 Rttn rotatin gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1550559 Rttn rotatin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11900971 1550559 Rttn rotatin gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11900971 1550559 Rttn rotatin gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1550559 Rttn rotatin gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11900971 1550559 Rttn rotatin gene MP:0002188 small heart IEA N RGD:5509061 20210826 MGI 1550559 Rttn rotatin gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1550559 Rttn rotatin gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11900971 1550559 Rttn rotatin gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:11900971 1550559 Rttn rotatin gene MP:0004712 notochord degeneration IAGP N RGD:5509061 20141003 MGI PMID:11900971 1550559 Rttn rotatin gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:11900971 1550559 Rttn rotatin gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 1550559 Rttn rotatin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11900971 1550559 Rttn rotatin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1550559 Rttn rotatin gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210826 MGI 1550559 Rttn rotatin gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1550561 Pitpnm1 phosphatidylinositol transfer protein, membrane-associated 1 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20200310 MGI PMID:23820044 1550561 Pitpnm1 phosphatidylinositol transfer protein, membrane-associated 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:23820044 1550561 Pitpnm1 phosphatidylinositol transfer protein, membrane-associated 1 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:23820044 1550561 Pitpnm1 phosphatidylinositol transfer protein, membrane-associated 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:23820044 1550561 Pitpnm1 phosphatidylinositol transfer protein, membrane-associated 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20200310 MGI 1550561 Pitpnm1 phosphatidylinositol transfer protein, membrane-associated 1 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20200310 MGI 1550564 Ddx5 DEAD box helicase 5 gene MP:0001147 small testis IAGP N RGD:5509061 20220707 MGI PMID:33666296 1550564 Ddx5 DEAD box helicase 5 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220707 MGI PMID:33666296 1550564 Ddx5 DEAD box helicase 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20220707 MGI PMID:33666296 1550564 Ddx5 DEAD box helicase 5 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:22986526 1550564 Ddx5 DEAD box helicase 5 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220707 MGI PMID:33666296 1550564 Ddx5 DEAD box helicase 5 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220707 MGI PMID:33666296 1550564 Ddx5 DEAD box helicase 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220707 MGI PMID:33666296 1550564 Ddx5 DEAD box helicase 5 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220707 MGI PMID:33666296 1550564 Ddx5 DEAD box helicase 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220707 MGI PMID:33666296 1550564 Ddx5 DEAD box helicase 5 gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20220707 MGI PMID:33666296 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0000745 tremors IAGP N RGD:5509061 20191114 MGI PMID:31201232 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20191114 MGI PMID:31201232 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20170504 MGI 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20201015 MGI PMID:24586199 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20201015 MGI PMID:24586199 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20191114 MGI PMID:31201232 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:23050017 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230601 MGI 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20191114 MGI PMID:31201232 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20191114 MGI PMID:31201232 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20191114 MGI PMID:31201232 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23050017 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20191114 MGI PMID:31201232 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20201015 MGI PMID:24586199 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20201015 MGI PMID:24586199 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0014372 decreased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:23050017 1550566 Arf4 ADP-ribosylation factor 4 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20240328 MGI PMID:23050017 1550568 Tmem38b transmembrane protein 38B gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0001177 atelectasis IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0001953 respiratory failure IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20200310 MGI PMID:17611541 1550568 Tmem38b transmembrane protein 38B gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20200310 MGI PMID:17611541 1550568 Tmem38b transmembrane protein 38B gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0003031 acidosis IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0004085 abnormal heartbeat IAGP N RGD:5509061 20200310 MGI PMID:17611541 1550568 Tmem38b transmembrane protein 38B gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20200310 MGI PMID:17611541 1550568 Tmem38b transmembrane protein 38B gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20200310 MGI PMID:17611541 1550568 Tmem38b transmembrane protein 38B gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0004781 abnormal surfactant composition IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0005039 hypoxia IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:17611541 1550568 Tmem38b transmembrane protein 38B gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0010889 small alveolar lamellar bodies IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0010890 decreased alveolar lamellar body number IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19515693 1550568 Tmem38b transmembrane protein 38B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17611541 1550568 Tmem38b transmembrane protein 38B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1550574 Oprl1 opioid receptor-like 1 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1550574 Oprl1 opioid receptor-like 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1550574 Oprl1 opioid receptor-like 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1550574 Oprl1 opioid receptor-like 1 gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 1550574 Oprl1 opioid receptor-like 1 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20200310 MGI PMID:9707118 1550574 Oprl1 opioid receptor-like 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20200310 MGI PMID:9707118 1550574 Oprl1 opioid receptor-like 1 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20200310 MGI PMID:15030410 1550574 Oprl1 opioid receptor-like 1 gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20200310 MGI PMID:9155012 1550574 Oprl1 opioid receptor-like 1 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20200310 MGI PMID:9660760 1550574 Oprl1 opioid receptor-like 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1550574 Oprl1 opioid receptor-like 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20200310 MGI PMID:9707118 1550574 Oprl1 opioid receptor-like 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1550574 Oprl1 opioid receptor-like 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1550574 Oprl1 opioid receptor-like 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20231207 MGI 1550574 Oprl1 opioid receptor-like 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 1550574 Oprl1 opioid receptor-like 1 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20200310 MGI PMID:16519664 1550574 Oprl1 opioid receptor-like 1 gene MP:0002735 abnormal chemical nociception IAGP N RGD:5509061 20200310 MGI PMID:12814369 1550574 Oprl1 opioid receptor-like 1 gene MP:0002735 abnormal chemical nociception IAGP N RGD:5509061 20200310 MGI PMID:9155012 1550574 Oprl1 opioid receptor-like 1 gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20200310 MGI PMID:9707118 1550574 Oprl1 opioid receptor-like 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20200310 MGI PMID:9707118 1550574 Oprl1 opioid receptor-like 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:12814369 1550574 Oprl1 opioid receptor-like 1 gene MP:0004597 increased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20200310 MGI PMID:9155012 1550574 Oprl1 opioid receptor-like 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1550574 Oprl1 opioid receptor-like 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20200310 MGI PMID:11027224 1550574 Oprl1 opioid receptor-like 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0000599 enlarged liver IEA N RGD:5509061 20210520 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210128 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0001304 cataract IEA N RGD:5509061 20220519 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1550576 Acoxl acyl-Coenzyme A oxidase-like gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22700726 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22700726 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20161229 MGI PMID:25066807 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0001500 decreased kindling response IAGP N RGD:5509061 20161229 MGI PMID:25066807 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20161229 MGI PMID:25066807 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:18488037 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20161229 MGI PMID:25066807 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:22700726 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0002806 abnormal conditioned emotional response IAGP N RGD:5509061 20161229 MGI PMID:25066807 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0003063 increased coping response IAGP N RGD:5509061 20161229 MGI PMID:25066807 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:22700726 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18488037 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:22700726 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20161229 MGI PMID:25066807 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0003627 abnormal leukocyte tethering or rolling IAGP N RGD:5509061 20141003 MGI PMID:17111351 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22700726 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:18488037 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20161229 MGI PMID:25066807 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:18488037 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:18488037 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:22700726 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0008831 abnormal insulin-like growth factor I level IAGP N RGD:5509061 20161229 MGI PMID:25066807 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0012286 decreased frequency of paradoxical sleep IAGP N RGD:5509061 20161229 MGI PMID:25066807 1550578 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:22700726 1550581 Rps6ka2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22997248 1550581 Rps6ka2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:22997248 1550581 Rps6ka2 ribosomal protein S6 kinase, polypeptide 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:22997248 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:16467359 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:16467359 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:16467359 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:18446812 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:18729207 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:16700072 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:18729207 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18257070 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16467359 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:18257070 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:16467359 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:18257070 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:18257070 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16467359 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0001934 increased litter size IAGP N RGD:5509061 20210325 MGI PMID:30942852 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16700072 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:18446812 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18729207 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0002772 brachypodia IAGP N RGD:5509061 20141003 MGI PMID:18446812 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:18257070 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18446812 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:16467359 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:18257070 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18257070 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20141003 MGI PMID:18729207 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:18446812 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:18446812 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:18446812 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:19079247 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:18446812 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0004635 short metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:18446812 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0004648 decreased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:16467359 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:18446812 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16467359 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:18257070 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19079247 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:18729207 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0006394 abnormal vertebral epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:18729207 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:18257070 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18446812 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0009874 abnormal interdigital cell death IAGP N RGD:5509061 20141003 MGI PMID:18729207 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16950124 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18257070 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16467359 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:16467359 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:18257070 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:18257070 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0012182 abnormal presomitic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18257070 1550582 Sfrp2 secreted frizzled-related protein 2 gene MP:0031411 increased ovulation rate IAGP N RGD:5509061 20220804 MGI PMID:30942852 1550583 Nup35 nucleoporin 35 gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20180517 MGI PMID:27427419 1550583 Nup35 nucleoporin 35 gene MP:0002083 premature death IAGP N RGD:5509061 20180517 MGI PMID:27427419 1550583 Nup35 nucleoporin 35 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20180517 MGI PMID:27427419 1550583 Nup35 nucleoporin 35 gene MP:0002731 megacolon IAGP N RGD:5509061 20180517 MGI PMID:27427419 1550583 Nup35 nucleoporin 35 gene MP:0008802 abnormal intestinal smooth muscle morphology IAGP N RGD:5509061 20180517 MGI PMID:27427419 1550583 Nup35 nucleoporin 35 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20190502 MGI 1550583 Nup35 nucleoporin 35 gene MP:0009536 abnormal interstitial cell of Cajal morphology IAGP N RGD:5509061 20180517 MGI PMID:27427419 1550583 Nup35 nucleoporin 35 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1550583 Nup35 nucleoporin 35 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550583 Nup35 nucleoporin 35 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20180517 MGI PMID:27427419 1550583 Nup35 nucleoporin 35 gene MP:0014033 abnormal submucosal gland morphology IAGP N RGD:5509061 20180517 MGI PMID:27427419 1550583 Nup35 nucleoporin 35 gene MP:0014221 increased colon goblet cell number IAGP N RGD:5509061 20180517 MGI PMID:27427419 1550583 Nup35 nucleoporin 35 gene MP:0014231 intestinal mucus accumulation IAGP N RGD:5509061 20180517 MGI PMID:27427419 1550586 Cuedc1 CUE domain containing 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20221215 MGI 1550586 Cuedc1 CUE domain containing 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20211021 MGI 1550586 Cuedc1 CUE domain containing 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20221215 MGI 1550586 Cuedc1 CUE domain containing 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20221215 MGI 1550588 Hcst hematopoietic cell signal transducer gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20231207 MGI 1550588 Hcst hematopoietic cell signal transducer gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:19251634 1550588 Hcst hematopoietic cell signal transducer gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19251634 1550588 Hcst hematopoietic cell signal transducer gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:19251634 1550588 Hcst hematopoietic cell signal transducer gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17100879 1550588 Hcst hematopoietic cell signal transducer gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:19251634 1550588 Hcst hematopoietic cell signal transducer gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15878887 1550588 Hcst hematopoietic cell signal transducer gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:17100879 1550588 Hcst hematopoietic cell signal transducer gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15878887 1550588 Hcst hematopoietic cell signal transducer gene MP:0004260 enlarged placenta IAGP N RGD:5509061 20141003 MGI PMID:15878887 1550588 Hcst hematopoietic cell signal transducer gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17100879 1550588 Hcst hematopoietic cell signal transducer gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:17100879 1550588 Hcst hematopoietic cell signal transducer gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17100879 1550588 Hcst hematopoietic cell signal transducer gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:19251634 1550588 Hcst hematopoietic cell signal transducer gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:19332875 1550588 Hcst hematopoietic cell signal transducer gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:12426564 1550588 Hcst hematopoietic cell signal transducer gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17100879 1550588 Hcst hematopoietic cell signal transducer gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:17100879 1550588 Hcst hematopoietic cell signal transducer gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17100879 1550588 Hcst hematopoietic cell signal transducer gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19332875 1550588 Hcst hematopoietic cell signal transducer gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12426564 1550588 Hcst hematopoietic cell signal transducer gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:19251634 1550588 Hcst hematopoietic cell signal transducer gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17100879 1550588 Hcst hematopoietic cell signal transducer gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15878887 1550588 Hcst hematopoietic cell signal transducer gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19332875 1550588 Hcst hematopoietic cell signal transducer gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:17100879 1550588 Hcst hematopoietic cell signal transducer gene MP:0008876 decreased uterine NK cell number IAGP N RGD:5509061 20141003 MGI PMID:15878887 1550588 Hcst hematopoietic cell signal transducer gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17100879 1550588 Hcst hematopoietic cell signal transducer gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1550588 Hcst hematopoietic cell signal transducer gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:19251634 1550588 Hcst hematopoietic cell signal transducer gene MP:0012529 abnormal decidua basalis morphology IAGP N RGD:5509061 20141003 MGI PMID:15878887 1550594 Ip6k2 inositol hexaphosphate kinase 2 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:19430495 1550594 Ip6k2 inositol hexaphosphate kinase 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20151224 MGI PMID:24657168 1550594 Ip6k2 inositol hexaphosphate kinase 2 gene MP:0003010 decreased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:19430495 1550594 Ip6k2 inositol hexaphosphate kinase 2 gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20151224 MGI PMID:24657168 1550594 Ip6k2 inositol hexaphosphate kinase 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:19430495 1550594 Ip6k2 inositol hexaphosphate kinase 2 gene MP:0004546 esophagus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19430495 1550594 Ip6k2 inositol hexaphosphate kinase 2 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20151224 MGI PMID:24657168 1550594 Ip6k2 inositol hexaphosphate kinase 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19430495 1550594 Ip6k2 inositol hexaphosphate kinase 2 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:19430495 1550594 Ip6k2 inositol hexaphosphate kinase 2 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:19430495 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0000154 rib fusion IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0000480 increased rib number IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0004259 small placenta IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0009879 abnormal arcus anterior morphology IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0012398 decreased nucleated erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550599 Pcgf6 polycomb group ring finger 6 gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20200310 MGI PMID:28304275 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200310 MGI 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20200310 MGI 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0001967 deafness IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0001967 deafness IAGP N RGD:5509061 20200310 MGI PMID:26677943 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20200310 MGI 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:26677943 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0004364 thin stria vascularis IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:26677943 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:26677943 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20200310 MGI PMID:26677943 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0004750 syndromic hearing loss IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20200310 MGI PMID:26677943 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0009517 abnormal salivary gland duct morphology IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:23979167 1550600 Marveld2 MARVEL (membrane-associating) domain containing 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:26677943 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:21350561 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:21350561 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:21350561 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:21350561 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21350561 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:21350561 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19946331 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:19946331 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:21350561 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:21350561 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21350561 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:21350561 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21350561 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21350561 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19946331 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0011198 absent proamniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:19946331 1550602 Usp7 ubiquitin specific peptidase 7 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:21350561 1550606 Rab11fip4 RAB11 family interacting protein 4 (class II) gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1550606 Rab11fip4 RAB11 family interacting protein 4 (class II) gene MP:0001399 hyperactivity IEA N RGD:5509061 20240627 MGI 1550606 Rab11fip4 RAB11 family interacting protein 4 (class II) gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1550606 Rab11fip4 RAB11 family interacting protein 4 (class II) gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201231 MGI 1550606 Rab11fip4 RAB11 family interacting protein 4 (class II) gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1550607 Igsf21 immunoglobulin superfamily, member 21 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20200310 MGI PMID:28864826 1550607 Igsf21 immunoglobulin superfamily, member 21 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20200310 MGI PMID:28864826 1550607 Igsf21 immunoglobulin superfamily, member 21 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:28864826 1550609 Trim55 tripartite motif-containing 55 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200827 MGI PMID:23512667 1550609 Trim55 tripartite motif-containing 55 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20200827 MGI PMID:23512667 1550609 Trim55 tripartite motif-containing 55 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0002083 premature death IAGP N RGD:5509061 20200827 MGI PMID:23512667 1550609 Trim55 tripartite motif-containing 55 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200827 MGI PMID:23512667 1550609 Trim55 tripartite motif-containing 55 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20200827 MGI PMID:23512667 1550609 Trim55 tripartite motif-containing 55 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20200827 MGI PMID:23512667 1550609 Trim55 tripartite motif-containing 55 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20200827 MGI PMID:23512667 1550609 Trim55 tripartite motif-containing 55 gene MP:0004094 abnormal M line morphology IAGP N RGD:5509061 20200827 MGI PMID:23512667 1550609 Trim55 tripartite motif-containing 55 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20200827 MGI PMID:23512667 1550609 Trim55 tripartite motif-containing 55 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210128 MGI 1550609 Trim55 tripartite motif-containing 55 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20200827 MGI PMID:23512667 1550609 Trim55 tripartite motif-containing 55 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0010226 increased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210128 MGI 1550609 Trim55 tripartite motif-containing 55 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200827 MGI PMID:23512667 1550609 Trim55 tripartite motif-containing 55 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200827 MGI PMID:23512667 1550609 Trim55 tripartite motif-containing 55 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20200827 MGI PMID:23512667 1550609 Trim55 tripartite motif-containing 55 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1550609 Trim55 tripartite motif-containing 55 gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20161124 MGI PMID:18157088 1550609 Trim55 tripartite motif-containing 55 gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:26452100 1550610 Pros1 protein S (alpha) gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:19567881 1550610 Pros1 protein S (alpha) gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:19567881 1550610 Pros1 protein S (alpha) gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19567881 1550610 Pros1 protein S (alpha) gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19567881 1550610 Pros1 protein S (alpha) gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19567881 1550610 Pros1 protein S (alpha) gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:19567881 1550610 Pros1 protein S (alpha) gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:19567881 1550610 Pros1 protein S (alpha) gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:19567881 1550610 Pros1 protein S (alpha) gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19567881 1550610 Pros1 protein S (alpha) gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0009275 bruising IAGP N RGD:5509061 20141003 MGI PMID:19567881 1550610 Pros1 protein S (alpha) gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19567881 1550610 Pros1 protein S (alpha) gene MP:0010022 brain vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19567881 1550610 Pros1 protein S (alpha) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:19729839 1550610 Pros1 protein S (alpha) gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:19567881 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0000753 paralysis IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22802532 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20230119 MGI 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230119 MGI 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:22802532 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:22802532 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0005237 abnormal olfactory tract morphology IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:22802532 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:22802532 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0009946 abnormal olfactory bulb layer morphology IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0009954 abnormal mitral cell morphology IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22802532 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20150122 MGI PMID:24448406 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1550611 Ptbp2 polypyrimidine tract binding protein 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20230119 MGI 1550612 Snip1 Smad nuclear interacting protein 1 gene MP:0001661 extended life span IAGP N RGD:5509061 20241031 MGI PMID:37027487 1550612 Snip1 Smad nuclear interacting protein 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20241031 MGI PMID:37027487 1550612 Snip1 Smad nuclear interacting protein 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20141003 MGI 1550612 Snip1 Smad nuclear interacting protein 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160804 MGI 1550612 Snip1 Smad nuclear interacting protein 1 gene MP:0006241 abnormal placement of pupils IEA N RGD:5509061 20141003 MGI 1550612 Snip1 Smad nuclear interacting protein 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20241031 MGI PMID:37027487 1550613 Zbtb24 zinc finger and BTB domain containing 24 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20200310 MGI 1550613 Zbtb24 zinc finger and BTB domain containing 24 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1550613 Zbtb24 zinc finger and BTB domain containing 24 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20221215 MGI 1550613 Zbtb24 zinc finger and BTB domain containing 24 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1550613 Zbtb24 zinc finger and BTB domain containing 24 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 1550613 Zbtb24 zinc finger and BTB domain containing 24 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20221215 MGI 1550613 Zbtb24 zinc finger and BTB domain containing 24 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20200310 MGI 1550613 Zbtb24 zinc finger and BTB domain containing 24 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:27466202 1550613 Zbtb24 zinc finger and BTB domain containing 24 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550617 Larp4b La ribonucleoprotein 4B gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1550617 Larp4b La ribonucleoprotein 4B gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210520 MGI 1550617 Larp4b La ribonucleoprotein 4B gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210520 MGI 1550619 Stk16 serine/threonine kinase 16 gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20210826 MGI 1550619 Stk16 serine/threonine kinase 16 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1550619 Stk16 serine/threonine kinase 16 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210520 MGI 1550619 Stk16 serine/threonine kinase 16 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1550620 Rhox5 reproductive homeobox 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:9769172 1550621 Creb3l4 cAMP responsive element binding protein 3-like 4 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16107712 1550621 Creb3l4 cAMP responsive element binding protein 3-like 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16107712 1550621 Creb3l4 cAMP responsive element binding protein 3-like 4 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:16999736 1550621 Creb3l4 cAMP responsive element binding protein 3-like 4 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:16999736 1550621 Creb3l4 cAMP responsive element binding protein 3-like 4 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:16107712 1550622 Hbb-bh1 hemoglobin Z, beta-like embryonic chain gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17077320 1550623 Ssc4d scavenger receptor cysteine rich family, 4 domains gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1550627 Sh2d2a SH2 domain containing 2A gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10587356 1550627 Sh2d2a SH2 domain containing 2A gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10587356 1550627 Sh2d2a SH2 domain containing 2A gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:10587356 1550627 Sh2d2a SH2 domain containing 2A gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:10587356 1550632 Glt8d1 glycosyltransferase 8 domain containing 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1550632 Glt8d1 glycosyltransferase 8 domain containing 1 gene MP:0002635 reduced sensorimotor gating IEA N RGD:5509061 20170406 MGI 1550636 Vil1 villin 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210520 MGI 1550636 Vil1 villin 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20200310 MGI PMID:10459016 1550636 Vil1 villin 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20200310 MGI PMID:23520048 1550636 Vil1 villin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:9438428 1550636 Vil1 villin 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1550636 Vil1 villin 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20210520 MGI 1550636 Vil1 villin 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 1550636 Vil1 villin 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1550636 Vil1 villin 1 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210520 MGI 1550637 Clk1 CDC-like kinase 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20200310 MGI 1550637 Clk1 CDC-like kinase 1 gene MP:0000334 decreased granulocyte number IEA N RGD:5509061 20200310 MGI 1550637 Clk1 CDC-like kinase 1 gene MP:0000745 tremors IEA N RGD:5509061 20200310 MGI 1550637 Clk1 CDC-like kinase 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20200310 MGI 1550637 Clk1 CDC-like kinase 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20200310 MGI 1550637 Clk1 CDC-like kinase 1 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20200310 MGI 1550637 Clk1 CDC-like kinase 1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20200310 MGI 1550637 Clk1 CDC-like kinase 1 gene MP:0005316 abnormal response to tactile stimuli IEA N RGD:5509061 20200310 MGI 1550638 Atp2b4 ATPase, Ca++ transporting, plasma membrane 4 gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:15178683 1550638 Atp2b4 ATPase, Ca++ transporting, plasma membrane 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15078889 1550638 Atp2b4 ATPase, Ca++ transporting, plasma membrane 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15178683 1550638 Atp2b4 ATPase, Ca++ transporting, plasma membrane 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15078889 1550638 Atp2b4 ATPase, Ca++ transporting, plasma membrane 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15178683 1550638 Atp2b4 ATPase, Ca++ transporting, plasma membrane 4 gene MP:0002742 enlarged submandibular lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15178683 1550638 Atp2b4 ATPase, Ca++ transporting, plasma membrane 4 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:15178683 1550638 Atp2b4 ATPase, Ca++ transporting, plasma membrane 4 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:15078889 1550638 Atp2b4 ATPase, Ca++ transporting, plasma membrane 4 gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20190829 MGI PMID:28714864 1550640 Id4 inhibitor of DNA binding 4 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20200310 MGI PMID:25038044 1550640 Id4 inhibitor of DNA binding 4 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:15469968 1550640 Id4 inhibitor of DNA binding 4 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:15469968 1550640 Id4 inhibitor of DNA binding 4 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20200310 MGI PMID:15469968 1550640 Id4 inhibitor of DNA binding 4 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20200310 MGI PMID:15469968 1550640 Id4 inhibitor of DNA binding 4 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20200310 MGI PMID:25038044 1550640 Id4 inhibitor of DNA binding 4 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20200310 MGI PMID:25038044 1550640 Id4 inhibitor of DNA binding 4 gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:20628571 1550640 Id4 inhibitor of DNA binding 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:20628571 1550640 Id4 inhibitor of DNA binding 4 gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:19217292 1550640 Id4 inhibitor of DNA binding 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:20628571 1550640 Id4 inhibitor of DNA binding 4 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:20628571 1550640 Id4 inhibitor of DNA binding 4 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0003371 decreased circulating estrogen level IAGP N RGD:5509061 20200310 MGI PMID:25038044 1550640 Id4 inhibitor of DNA binding 4 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20200310 MGI PMID:20628571 1550640 Id4 inhibitor of DNA binding 4 gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20200310 MGI PMID:25038044 1550640 Id4 inhibitor of DNA binding 4 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20200310 MGI PMID:20628571 1550640 Id4 inhibitor of DNA binding 4 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20200310 MGI PMID:25038044 1550640 Id4 inhibitor of DNA binding 4 gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20200310 MGI PMID:20628571 1550640 Id4 inhibitor of DNA binding 4 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20200310 MGI PMID:15469968 1550640 Id4 inhibitor of DNA binding 4 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0008870 increased mature ovarian follicle number IAGP N RGD:5509061 20200310 MGI PMID:25038044 1550640 Id4 inhibitor of DNA binding 4 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20200310 MGI PMID:20628571 1550640 Id4 inhibitor of DNA binding 4 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20200310 MGI PMID:15469968 1550640 Id4 inhibitor of DNA binding 4 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15882580 1550640 Id4 inhibitor of DNA binding 4 gene MP:0011128 increased tertiary ovarian follicle number IAGP N RGD:5509061 20200310 MGI PMID:25038044 1550640 Id4 inhibitor of DNA binding 4 gene MP:0013609 abnormal ovarian medulla morphology IAGP N RGD:5509061 20200310 MGI PMID:25038044 1550640 Id4 inhibitor of DNA binding 4 gene MP:0013778 abnormal mammary gland myoepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:25038044 1550640 Id4 inhibitor of DNA binding 4 gene MP:0013781 abnormal mammary gland luminal epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:25038044 1550640 Id4 inhibitor of DNA binding 4 gene MP:0013908 small lateral ventricles IAGP N RGD:5509061 20200310 MGI PMID:15469968 1550640 Id4 inhibitor of DNA binding 4 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20200310 MGI PMID:20628571 1550640 Id4 inhibitor of DNA binding 4 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:20628571 1550640 Id4 inhibitor of DNA binding 4 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:25038044 1550640 Id4 inhibitor of DNA binding 4 gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:25038044 1550646 Yif1b Yip1 interacting factor homolog B (S. cerevisiae) gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20200402 MGI PMID:26077767 1550646 Yif1b Yip1 interacting factor homolog B (S. cerevisiae) gene MP:0030949 abnormal Golgi vesicle transport IAGP N RGD:5509061 20200402 MGI PMID:26077767 1550646 Yif1b Yip1 interacting factor homolog B (S. cerevisiae) gene MP:0030953 abnormal Golgi cisterna morphology IAGP N RGD:5509061 20200402 MGI PMID:26077767 1550647 Unc13d unc-13 homolog D gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17420270 1550647 Unc13d unc-13 homolog D gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17420270 1550647 Unc13d unc-13 homolog D gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17420270 1550647 Unc13d unc-13 homolog D gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17420270 1550647 Unc13d unc-13 homolog D gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:17420270 1550647 Unc13d unc-13 homolog D gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16688530 1550647 Unc13d unc-13 homolog D gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17420270 1550647 Unc13d unc-13 homolog D gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17420270 1550647 Unc13d unc-13 homolog D gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:17420270 1550647 Unc13d unc-13 homolog D gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20160714 MGI PMID:23659589 1550647 Unc13d unc-13 homolog D gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20160714 MGI PMID:23659589 1550647 Unc13d unc-13 homolog D gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20160714 MGI PMID:23659589 1550647 Unc13d unc-13 homolog D gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17420270 1550647 Unc13d unc-13 homolog D gene MP:0008523 absent lymph node germinal center IAGP N RGD:5509061 20141003 MGI PMID:17420270 1550647 Unc13d unc-13 homolog D gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20200310 MGI PMID:23659589 1550647 Unc13d unc-13 homolog D gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20160714 MGI PMID:23659589 1550647 Unc13d unc-13 homolog D gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17420270 1550647 Unc13d unc-13 homolog D gene MP:0020215 impaired blood coagulation IAGP N RGD:5509061 20160714 MGI PMID:23659589 1550647 Unc13d unc-13 homolog D gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:16688530 1550647 Unc13d unc-13 homolog D gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:17420270 1550647 Unc13d unc-13 homolog D gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:16688530 1550647 Unc13d unc-13 homolog D gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:17420270 1550647 Unc13d unc-13 homolog D gene MP:0031070 hemophagocytosis IAGP N RGD:5509061 20200618 MGI PMID:17420270 1550649 Cltb clathrin light chain B gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20230216 MGI PMID:32907943 1550649 Cltb clathrin light chain B gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20230216 MGI PMID:32907943 1550649 Cltb clathrin light chain B gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20230216 MGI PMID:32907943 1550650 Uxt ubiquitously expressed prefoldin like chaperone gene MP:0001147 small testis IAGP N RGD:5509061 20180614 MGI PMID:29649254 1550650 Uxt ubiquitously expressed prefoldin like chaperone gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20180614 MGI PMID:29649254 1550650 Uxt ubiquitously expressed prefoldin like chaperone gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180614 MGI PMID:29649254 1550650 Uxt ubiquitously expressed prefoldin like chaperone gene MP:0005159 azoospermia IAGP N RGD:5509061 20180614 MGI PMID:29649254 1550650 Uxt ubiquitously expressed prefoldin like chaperone gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20180614 MGI PMID:29649254 1550650 Uxt ubiquitously expressed prefoldin like chaperone gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20180614 MGI PMID:29649254 1550650 Uxt ubiquitously expressed prefoldin like chaperone gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20180614 MGI PMID:29649254 1550650 Uxt ubiquitously expressed prefoldin like chaperone gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20180614 MGI PMID:29649254 1550651 Uba1 ubiquitin-like modifier activating enzyme 1 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20220630 MGI PMID:35440748 1550651 Uba1 ubiquitin-like modifier activating enzyme 1 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20220630 MGI PMID:35440748 1550651 Uba1 ubiquitin-like modifier activating enzyme 1 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20220630 MGI PMID:35440748 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16467350 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16467350 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:16467350 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16467350 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16467350 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0003121 genetic imprinting IAGP N RGD:5509061 20141003 MGI PMID:16467350 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16467350 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:16467350 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16467350 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20141003 MGI PMID:16467350 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16467350 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16467350 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16467350 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16467350 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16467350 1550653 Abcb7 ATP-binding cassette, sub-family B member 7 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:16467350 1550654 Pdcd10 programmed cell death 10 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:21490399 1550654 Pdcd10 programmed cell death 10 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:21490399 1550654 Pdcd10 programmed cell death 10 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21490399 1550654 Pdcd10 programmed cell death 10 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21490399 1550654 Pdcd10 programmed cell death 10 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20180614 MGI PMID:24176643 1550654 Pdcd10 programmed cell death 10 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20190307 MGI PMID:25625206 1550654 Pdcd10 programmed cell death 10 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21859843 1550654 Pdcd10 programmed cell death 10 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21490399 1550654 Pdcd10 programmed cell death 10 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20180614 MGI PMID:24176643 1550654 Pdcd10 programmed cell death 10 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:21490399 1550654 Pdcd10 programmed cell death 10 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21490399 1550654 Pdcd10 programmed cell death 10 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21859843 1550654 Pdcd10 programmed cell death 10 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20180614 MGI PMID:24176643 1550654 Pdcd10 programmed cell death 10 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20180614 MGI PMID:24176643 1550654 Pdcd10 programmed cell death 10 gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:21490399 1550654 Pdcd10 programmed cell death 10 gene MP:0009382 abnormal cardiac jelly morphology IAGP N RGD:5509061 20190307 MGI PMID:25625206 1550654 Pdcd10 programmed cell death 10 gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21490399 1550654 Pdcd10 programmed cell death 10 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21490399 1550654 Pdcd10 programmed cell death 10 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190307 MGI PMID:25625206 1550654 Pdcd10 programmed cell death 10 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550654 Pdcd10 programmed cell death 10 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20371769 1550654 Pdcd10 programmed cell death 10 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:21321212 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:14560010 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20200310 MGI PMID:17635993 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:17635993 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20200310 MGI PMID:17635993 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0000404 decreased curvature of zigzag hairs IAGP N RGD:5509061 20200310 MGI PMID:17635993 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0000416 sparse hair IAGP N RGD:5509061 20200310 MGI PMID:17635993 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:21258009 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:17635993 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20200310 MGI PMID:17635993 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20200310 MGI PMID:14560010 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20200310 MGI PMID:14560010 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:14560010 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:21258009 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:21258009 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20200310 MGI PMID:14560010 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:14560010 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:14560010 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20200310 MGI PMID:14560010 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:14560010 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:17635993 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:21258009 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20200310 MGI PMID:21258009 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0005409 darkened coat color IAGP N RGD:5509061 20200310 MGI PMID:17635993 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:14560010 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:21258009 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20200310 MGI PMID:21258009 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0008538 decreased zigzag hair amount IAGP N RGD:5509061 20200310 MGI PMID:17635993 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:17635993 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0010130 decreased DN1 thymic pro-T cell number IAGP N RGD:5509061 20200310 MGI PMID:21258009 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0010132 decreased DN2 thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:21258009 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0010134 decreased DN3 thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:21258009 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0010179 rough coat IAGP N RGD:5509061 20200310 MGI PMID:17635993 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0010202 focal dorsal hair loss IAGP N RGD:5509061 20200310 MGI PMID:17635993 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:14560010 1550658 Zbtb17 zinc finger and BTB domain containing 17 gene MP:0011198 absent proamniotic cavity IAGP N RGD:5509061 20200310 MGI PMID:14560010 1550659 Gaa glucosidase, alpha, acid gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10838256 1550659 Gaa glucosidase, alpha, acid gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231102 MGI PMID:9384603 1550659 Gaa glucosidase, alpha, acid gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9384603 1550659 Gaa glucosidase, alpha, acid gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9384603 1550659 Gaa glucosidase, alpha, acid gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9384603 1550659 Gaa glucosidase, alpha, acid gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:9668092 1550659 Gaa glucosidase, alpha, acid gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:10838256 1550659 Gaa glucosidase, alpha, acid gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:15674828 1550659 Gaa glucosidase, alpha, acid gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:9668092 1550659 Gaa glucosidase, alpha, acid gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:10838256 1550659 Gaa glucosidase, alpha, acid gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:10838256 1550659 Gaa glucosidase, alpha, acid gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10838256 1550659 Gaa glucosidase, alpha, acid gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9668092 1550659 Gaa glucosidase, alpha, acid gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10838256 1550659 Gaa glucosidase, alpha, acid gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10838256 1550659 Gaa glucosidase, alpha, acid gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9668092 1550659 Gaa glucosidase, alpha, acid gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:15674828 1550659 Gaa glucosidase, alpha, acid gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:15674828 1550659 Gaa glucosidase, alpha, acid gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9384603 1550659 Gaa glucosidase, alpha, acid gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:9384603 1550659 Gaa glucosidase, alpha, acid gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:9384603 1550659 Gaa glucosidase, alpha, acid gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:9668092 1550659 Gaa glucosidase, alpha, acid gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9384603 1550659 Gaa glucosidase, alpha, acid gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:9384603 1550659 Gaa glucosidase, alpha, acid gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20150416 MGI PMID:25036864 1550659 Gaa glucosidase, alpha, acid gene MP:0003898 abnormal QRS complex IAGP N RGD:5509061 20141003 MGI PMID:9384603 1550659 Gaa glucosidase, alpha, acid gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9668092 1550659 Gaa glucosidase, alpha, acid gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:9668092 1550659 Gaa glucosidase, alpha, acid gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:9668092 1550659 Gaa glucosidase, alpha, acid gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:15674828 1550659 Gaa glucosidase, alpha, acid gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:9668092 1550659 Gaa glucosidase, alpha, acid gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:10838256 1550659 Gaa glucosidase, alpha, acid gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:9384603 1550659 Gaa glucosidase, alpha, acid gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:9668092 1550659 Gaa glucosidase, alpha, acid gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9384603 1550659 Gaa glucosidase, alpha, acid gene MP:0005440 increased glycogen level IAGP N RGD:5509061 20150416 MGI PMID:25036864 1550659 Gaa glucosidase, alpha, acid gene MP:0006087 increased body mass index IAGP N RGD:5509061 20141003 MGI PMID:15674828 1550659 Gaa glucosidase, alpha, acid gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:9668092 1550659 Gaa glucosidase, alpha, acid gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20211028 MGI PMID:27358407 1550659 Gaa glucosidase, alpha, acid gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:10838256 1550659 Gaa glucosidase, alpha, acid gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:11785984 1550659 Gaa glucosidase, alpha, acid gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:9668092 1550659 Gaa glucosidase, alpha, acid gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20150416 MGI PMID:25036864 1550659 Gaa glucosidase, alpha, acid gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20211028 MGI PMID:27358407 1550659 Gaa glucosidase, alpha, acid gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20160310 MGI PMID:10838256 1550659 Gaa glucosidase, alpha, acid gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20160310 MGI PMID:9668092 1550659 Gaa glucosidase, alpha, acid gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20211028 MGI PMID:27358407 1550659 Gaa glucosidase, alpha, acid gene MP:0014074 increased brain glycogen level IAGP N RGD:5509061 20160310 MGI PMID:10838256 1550659 Gaa glucosidase, alpha, acid gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:9384603 1550660 Gsn gelsolin gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:10684249 1550660 Gsn gelsolin gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7720072 1550660 Gsn gelsolin gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:7720072 1550660 Gsn gelsolin gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:10985859 1550660 Gsn gelsolin gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:10684249 1550660 Gsn gelsolin gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:10684249 1550660 Gsn gelsolin gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:7720072 1550660 Gsn gelsolin gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:11514591 1550660 Gsn gelsolin gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:7720072 1550660 Gsn gelsolin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9927495 1550660 Gsn gelsolin gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:9927495 1550660 Gsn gelsolin gene MP:0002295 abnormal pulmonary circulation IAGP N RGD:5509061 20141003 MGI PMID:12654637 1550660 Gsn gelsolin gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11514591 1550660 Gsn gelsolin gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:10684249 1550660 Gsn gelsolin gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10684249 1550660 Gsn gelsolin gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:12654637 1550660 Gsn gelsolin gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:9927495 1550660 Gsn gelsolin gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:10684249 1550660 Gsn gelsolin gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:10684249 1550660 Gsn gelsolin gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:7720072 1550660 Gsn gelsolin gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10684249 1550660 Gsn gelsolin gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:7720072 1550660 Gsn gelsolin gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:9927495 1550660 Gsn gelsolin gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:10985859 1550660 Gsn gelsolin gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20201001 MGI PMID:7720072 1550660 Gsn gelsolin gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:10684249 1550660 Gsn gelsolin gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:7720072 1550660 Gsn gelsolin gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:7720072 1550660 Gsn gelsolin gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10985859 1550660 Gsn gelsolin gene MP:0013782 abnormal mammary duct terminal end bud morphology IAGP N RGD:5509061 20150625 MGI PMID:10985859 1550670 H2-T3 histocompatibility 2, T region locus 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19004778 1550670 H2-T3 histocompatibility 2, T region locus 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20880997 1550670 H2-T3 histocompatibility 2, T region locus 3 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:19004778 1550670 H2-T3 histocompatibility 2, T region locus 3 gene MP:0008361 abnormal CD8-positive, gamma-delta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19004778 1550670 H2-T3 histocompatibility 2, T region locus 3 gene MP:0008401 abnormal CD8 positive, alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19004778 1550670 H2-T3 histocompatibility 2, T region locus 3 gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19004778 1550670 H2-T3 histocompatibility 2, T region locus 3 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19004778 1550670 H2-T3 histocompatibility 2, T region locus 3 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19004778 1550670 H2-T3 histocompatibility 2, T region locus 3 gene MP:0008894 abnormal intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19004778 1550670 H2-T3 histocompatibility 2, T region locus 3 gene MP:0008895 abnormal intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:19004778 1550671 Eogt EGF domain specific O-linked N-acetylglucosamine transferase gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20240530 MGI PMID:28395734 1550671 Eogt EGF domain specific O-linked N-acetylglucosamine transferase gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1550671 Eogt EGF domain specific O-linked N-acetylglucosamine transferase gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20240530 MGI PMID:28395734 1550671 Eogt EGF domain specific O-linked N-acetylglucosamine transferase gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20240530 MGI PMID:28395734 1550671 Eogt EGF domain specific O-linked N-acetylglucosamine transferase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1550672 Six3 sine oculis-related homeobox 3 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:12569128 1550672 Six3 sine oculis-related homeobox 3 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:18694563 1550672 Six3 sine oculis-related homeobox 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12569128 1550672 Six3 sine oculis-related homeobox 3 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:18694563 1550672 Six3 sine oculis-related homeobox 3 gene MP:0001288 abnormal lens induction IAGP N RGD:5509061 20141003 MGI PMID:17066077 1550672 Six3 sine oculis-related homeobox 3 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:17066077 1550672 Six3 sine oculis-related homeobox 3 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:12569128 1550672 Six3 sine oculis-related homeobox 3 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:17066077 1550672 Six3 sine oculis-related homeobox 3 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:17066077 1550672 Six3 sine oculis-related homeobox 3 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:17066077 1550672 Six3 sine oculis-related homeobox 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12569128 1550672 Six3 sine oculis-related homeobox 3 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:18694563 1550672 Six3 sine oculis-related homeobox 3 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17066077 1550672 Six3 sine oculis-related homeobox 3 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:17066077 1550672 Six3 sine oculis-related homeobox 3 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:12569128 1550672 Six3 sine oculis-related homeobox 3 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:17066077 1550672 Six3 sine oculis-related homeobox 3 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:17066077 1550672 Six3 sine oculis-related homeobox 3 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:18694563 1550672 Six3 sine oculis-related homeobox 3 gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20141003 MGI PMID:18694563 1550672 Six3 sine oculis-related homeobox 3 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:18694563 1550672 Six3 sine oculis-related homeobox 3 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12569128 1550672 Six3 sine oculis-related homeobox 3 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:17066077 1550672 Six3 sine oculis-related homeobox 3 gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20141003 MGI PMID:18694563 1550672 Six3 sine oculis-related homeobox 3 gene MP:0006293 absent nasal placodes IAGP N RGD:5509061 20141003 MGI PMID:12569128 1550672 Six3 sine oculis-related homeobox 3 gene MP:0006294 absent optic vesicle IAGP N RGD:5509061 20141003 MGI PMID:12569128 1550672 Six3 sine oculis-related homeobox 3 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:18694563 1550672 Six3 sine oculis-related homeobox 3 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:18694563 1550672 Six3 sine oculis-related homeobox 3 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:18694563 1550672 Six3 sine oculis-related homeobox 3 gene MP:0010059 olfactory bulb hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18694563 1550672 Six3 sine oculis-related homeobox 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12569128 1550672 Six3 sine oculis-related homeobox 3 gene MP:0012091 increased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:12569128 1550672 Six3 sine oculis-related homeobox 3 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:12569128 1550672 Six3 sine oculis-related homeobox 3 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:17066077 1550672 Six3 sine oculis-related homeobox 3 gene MP:0012257 absent philtrum IAGP N RGD:5509061 20141003 MGI PMID:18694563 1550672 Six3 sine oculis-related homeobox 3 gene MP:0013906 absent embryonic telencephalon IAGP N RGD:5509061 20150924 MGI PMID:12569128 1550672 Six3 sine oculis-related homeobox 3 gene MP:0030241 absent optic pit IAGP N RGD:5509061 20171109 MGI PMID:12569128 1550674 Mpzl2 myelin protein zero-like 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20210128 MGI 1550674 Mpzl2 myelin protein zero-like 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 1550674 Mpzl2 myelin protein zero-like 2 gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20210128 MGI 1550674 Mpzl2 myelin protein zero-like 2 gene MP:0004357 long tibia IEA N RGD:5509061 20210128 MGI 1550674 Mpzl2 myelin protein zero-like 2 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20200310 MGI 1550674 Mpzl2 myelin protein zero-like 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1550674 Mpzl2 myelin protein zero-like 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1550674 Mpzl2 myelin protein zero-like 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1550676 Ablim2 actin-binding LIM protein 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20221103 MGI 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20221103 MGI 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20221103 MGI 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0004357 long tibia IEA N RGD:5509061 20221103 MGI 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20221103 MGI 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20221103 MGI 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0011999 abnormal tail length IEA N RGD:5509061 20221103 MGI 1550677 Micu1 mitochondrial calcium uptake 1 gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20201015 MGI PMID:27477272 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230119 MGI 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20220602 MGI PMID:35422047 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20220602 MGI PMID:35422047 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:23217742 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220602 MGI PMID:35422047 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:23217742 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0002083 premature death IAGP N RGD:5509061 20220602 MGI PMID:35422047 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:23217742 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:23217742 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20230119 MGI 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20220602 MGI PMID:35422047 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20220602 MGI PMID:35422047 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20220602 MGI PMID:35422047 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20220602 MGI PMID:35422047 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20220602 MGI PMID:35422047 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:23217742 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:23217742 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0009695 abnormal spinal cord ventral commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:23217742 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20220602 MGI PMID:35422047 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20220602 MGI PMID:35422047 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20220602 MGI PMID:35422047 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23217742 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20141003 MGI PMID:23217742 1550679 Crppa CDP-L-ribitol pyrophosphorylase A gene MP:0020391 radial glial endfoot detachment IAGP N RGD:5509061 20161117 MGI PMID:23217742 1550682 Mybpc1 myosin binding protein C, slow-type gene MP:0000160 kyphosis IEA N RGD:5509061 20220407 MGI 1550682 Mybpc1 myosin binding protein C, slow-type gene MP:0000745 tremors IEA N RGD:5509061 20220407 MGI 1550682 Mybpc1 myosin binding protein C, slow-type gene MP:0001265 decreased body size IEA N RGD:5509061 20220407 MGI 1550682 Mybpc1 myosin binding protein C, slow-type gene MP:0002058 neonatal lethality IEA N RGD:5509061 20220407 MGI 1550682 Mybpc1 myosin binding protein C, slow-type gene MP:0002082 postnatal lethality IEA N RGD:5509061 20220407 MGI 1550682 Mybpc1 myosin binding protein C, slow-type gene MP:0004090 abnormal sarcomere morphology IEA N RGD:5509061 20220407 MGI 1550682 Mybpc1 myosin binding protein C, slow-type gene MP:0004819 decreased skeletal muscle mass IEA N RGD:5509061 20220407 MGI 1550682 Mybpc1 myosin binding protein C, slow-type gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220407 MGI 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001147 small testis IAGP N RGD:5509061 20211216 MGI PMID:34100066 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20211216 MGI PMID:34100066 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20200310 MGI 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20211216 MGI PMID:34100066 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20211216 MGI PMID:34100066 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:15782166 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20200310 MGI PMID:15782166 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:20103643 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:20103643 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20200310 MGI PMID:20103643 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20211216 MGI PMID:34100066 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:15782166 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20211216 MGI PMID:34100066 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220407 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20211216 MGI PMID:34100066 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20211216 MGI PMID:34100066 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200310 MGI 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17415412 1550683 Ewsr1 Ewing sarcoma breakpoint region 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20200310 MGI PMID:20103643 1550688 Slc41a2 solute carrier family 41, member 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1550688 Slc41a2 solute carrier family 41, member 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1550688 Slc41a2 solute carrier family 41, member 2 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20211021 MGI 1550689 Fut8 fucosyltransferase 8 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20180628 MGI 1550689 Fut8 fucosyltransferase 8 gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20180628 MGI 1550689 Fut8 fucosyltransferase 8 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:16236725 1550689 Fut8 fucosyltransferase 8 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16236725 1550689 Fut8 fucosyltransferase 8 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:16236725 1550689 Fut8 fucosyltransferase 8 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:16236725 1550689 Fut8 fucosyltransferase 8 gene MP:0002338 abnormal pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:16236725 1550689 Fut8 fucosyltransferase 8 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16236725 1550689 Fut8 fucosyltransferase 8 gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20180628 MGI 1550689 Fut8 fucosyltransferase 8 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20180628 MGI 1550689 Fut8 fucosyltransferase 8 gene MP:0006054 spinal hemorrhage IEA N RGD:5509061 20180628 MGI 1550689 Fut8 fucosyltransferase 8 gene MP:0006093 arteriovenous malformation IEA N RGD:5509061 20180628 MGI 1550689 Fut8 fucosyltransferase 8 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19179362 1550689 Fut8 fucosyltransferase 8 gene MP:0010668 abnormal hepatic portal vein morphology IEA N RGD:5509061 20180628 MGI 1550689 Fut8 fucosyltransferase 8 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:16236725 1550689 Fut8 fucosyltransferase 8 gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:16236725 1550689 Fut8 fucosyltransferase 8 gene MP:0010903 abnormal pulmonary alveolus wall morphology IAGP N RGD:5509061 20141003 MGI PMID:19179362 1550689 Fut8 fucosyltransferase 8 gene MP:0010908 dilated pulmonary alveolar duct IAGP N RGD:5509061 20141003 MGI PMID:16236725 1550689 Fut8 fucosyltransferase 8 gene MP:0010937 increased total lung capacity IAGP N RGD:5509061 20141003 MGI PMID:16236725 1550689 Fut8 fucosyltransferase 8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16236725 1550689 Fut8 fucosyltransferase 8 gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20180628 MGI 1550689 Fut8 fucosyltransferase 8 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20180628 MGI 1550689 Fut8 fucosyltransferase 8 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20180628 MGI 1550689 Fut8 fucosyltransferase 8 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20180628 MGI 1550689 Fut8 fucosyltransferase 8 gene MP:0014018 embryo tumor IEA N RGD:5509061 20180628 MGI 1550689 Fut8 fucosyltransferase 8 gene MP:0014023 abnormal intestine placement IEA N RGD:5509061 20180628 MGI 1550690 Synrg synergin, gamma gene MP:0002626 increased heart rate IEA N RGD:5509061 20201022 MGI 1550690 Synrg synergin, gamma gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550691 Lrrc8c leucine rich repeat containing 8 family, member C gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20221215 MGI 1550691 Lrrc8c leucine rich repeat containing 8 family, member C gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1550691 Lrrc8c leucine rich repeat containing 8 family, member C gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210520 MGI 1550691 Lrrc8c leucine rich repeat containing 8 family, member C gene MP:0001147 small testis IEA N RGD:5509061 20210520 MGI 1550691 Lrrc8c leucine rich repeat containing 8 family, member C gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:21804215 1550691 Lrrc8c leucine rich repeat containing 8 family, member C gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1550691 Lrrc8c leucine rich repeat containing 8 family, member C gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200310 MGI PMID:21804215 1550691 Lrrc8c leucine rich repeat containing 8 family, member C gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20200310 MGI PMID:21804215 1550691 Lrrc8c leucine rich repeat containing 8 family, member C gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20221215 MGI 1550691 Lrrc8c leucine rich repeat containing 8 family, member C gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:21804215 1550691 Lrrc8c leucine rich repeat containing 8 family, member C gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1550692 Inmt indolethylamine N-methyltransferase gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1550692 Inmt indolethylamine N-methyltransferase gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1550692 Inmt indolethylamine N-methyltransferase gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20220519 MGI 1550694 F8 coagulation factor VIII gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:21705497 1550694 F8 coagulation factor VIII gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:7647782 1550694 F8 coagulation factor VIII gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:8896409 1550694 F8 coagulation factor VIII gene MP:0005000 abnormal immune tolerance IAGP N RGD:5509061 20141003 MGI PMID:16493498 1550694 F8 coagulation factor VIII gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:7647782 1550694 F8 coagulation factor VIII gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:8896409 1550694 F8 coagulation factor VIII gene MP:0012328 decreased circulating factor VIII level IAGP N RGD:5509061 20141003 MGI PMID:24705491 1550695 Dner delta/notch-like EGF repeat containing gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:16298139 1550695 Dner delta/notch-like EGF repeat containing gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:16298139 1550695 Dner delta/notch-like EGF repeat containing gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15965470 1550695 Dner delta/notch-like EGF repeat containing gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15965470 1550695 Dner delta/notch-like EGF repeat containing gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1550695 Dner delta/notch-like EGF repeat containing gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16298139 1550695 Dner delta/notch-like EGF repeat containing gene MP:0002763 ectopic Bergmann glia cells IAGP N RGD:5509061 20141003 MGI PMID:15965470 1550695 Dner delta/notch-like EGF repeat containing gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16298139 1550695 Dner delta/notch-like EGF repeat containing gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20141003 MGI PMID:16298139 1550695 Dner delta/notch-like EGF repeat containing gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1550695 Dner delta/notch-like EGF repeat containing gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:16298139 1550696 Galnt18 polypeptide N-acetylgalactosaminyltransferase 18 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1550696 Galnt18 polypeptide N-acetylgalactosaminyltransferase 18 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200310 MGI 1550696 Galnt18 polypeptide N-acetylgalactosaminyltransferase 18 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20201231 MGI 1550696 Galnt18 polypeptide N-acetylgalactosaminyltransferase 18 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200310 MGI 1550696 Galnt18 polypeptide N-acetylgalactosaminyltransferase 18 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20200310 MGI 1550696 Galnt18 polypeptide N-acetylgalactosaminyltransferase 18 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20200310 MGI 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0000433 microcephaly IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0010939 abnormal mandibular prominence morphology IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550697 Mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20200310 MGI PMID:23267094 1550698 Klhl17 kelch-like 17 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20240523 MGI 1550698 Klhl17 kelch-like 17 gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20240523 MGI 1550698 Klhl17 kelch-like 17 gene MP:0001406 abnormal gait IEA N RGD:5509061 20240523 MGI 1550698 Klhl17 kelch-like 17 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20210819 MGI PMID:33256713 1550698 Klhl17 kelch-like 17 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20210819 MGI PMID:33256713 1550698 Klhl17 kelch-like 17 gene MP:0014373 increased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:33256713 1550698 Klhl17 kelch-like 17 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20210819 MGI PMID:33256713 1550698 Klhl17 kelch-like 17 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:33256713 1550700 Stk36 serine/threonine kinase 36 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200310 MGI PMID:21746835 1550700 Stk36 serine/threonine kinase 36 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20200310 MGI PMID:16055717 1550700 Stk36 serine/threonine kinase 36 gene MP:0000440 domed cranium IAGP N RGD:5509061 20200310 MGI PMID:16055717 1550700 Stk36 serine/threonine kinase 36 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20200310 MGI PMID:16055717 1550700 Stk36 serine/threonine kinase 36 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20200310 MGI PMID:16055717 1550700 Stk36 serine/threonine kinase 36 gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:21746835 1550700 Stk36 serine/threonine kinase 36 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:16055716 1550700 Stk36 serine/threonine kinase 36 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:21746835 1550700 Stk36 serine/threonine kinase 36 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:16055717 1550700 Stk36 serine/threonine kinase 36 gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:16055717 1550700 Stk36 serine/threonine kinase 36 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:16055716 1550700 Stk36 serine/threonine kinase 36 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:16055717 1550700 Stk36 serine/threonine kinase 36 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:21746835 1550700 Stk36 serine/threonine kinase 36 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20200310 MGI PMID:21746835 1550700 Stk36 serine/threonine kinase 36 gene MP:0001867 rhinitis IAGP N RGD:5509061 20200310 MGI PMID:16055717 1550700 Stk36 serine/threonine kinase 36 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200310 MGI PMID:21746835 1550700 Stk36 serine/threonine kinase 36 gene MP:0001893 non-obstructive hydrocephaly IAGP N RGD:5509061 20200310 MGI PMID:16055717 1550700 Stk36 serine/threonine kinase 36 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:16055717 1550700 Stk36 serine/threonine kinase 36 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:24525297 1550700 Stk36 serine/threonine kinase 36 gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:21746835 1550700 Stk36 serine/threonine kinase 36 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21746835 1550700 Stk36 serine/threonine kinase 36 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:24525297 1550700 Stk36 serine/threonine kinase 36 gene MP:0002959 increased urine microalbumin level IEA N RGD:5509061 20211021 MGI 1550700 Stk36 serine/threonine kinase 36 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20200310 MGI PMID:16055717 1550700 Stk36 serine/threonine kinase 36 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20200310 MGI PMID:16055717 1550700 Stk36 serine/threonine kinase 36 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20231207 MGI 1550700 Stk36 serine/threonine kinase 36 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20200310 MGI PMID:24525297 1550700 Stk36 serine/threonine kinase 36 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20200310 MGI PMID:24525297 1550700 Stk36 serine/threonine kinase 36 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1550700 Stk36 serine/threonine kinase 36 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20200310 MGI PMID:24525297 1550700 Stk36 serine/threonine kinase 36 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:24525297 1550700 Stk36 serine/threonine kinase 36 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20200310 MGI PMID:24525297 1550700 Stk36 serine/threonine kinase 36 gene MP:0009280 decreased activated sperm motility IAGP N RGD:5509061 20200310 MGI PMID:24525297 1550700 Stk36 serine/threonine kinase 36 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20200310 MGI PMID:24525297 1550700 Stk36 serine/threonine kinase 36 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20200310 MGI PMID:24525297 1550700 Stk36 serine/threonine kinase 36 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20200310 MGI PMID:24525297 1550700 Stk36 serine/threonine kinase 36 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16055717 1550700 Stk36 serine/threonine kinase 36 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16055716 1550700 Stk36 serine/threonine kinase 36 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20200310 MGI PMID:24525297 1550700 Stk36 serine/threonine kinase 36 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20200310 MGI PMID:24525297 1550700 Stk36 serine/threonine kinase 36 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20220428 MGI PMID:24525297 1550701 Hs3st3b1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1550701 Hs3st3b1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1550701 Hs3st3b1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1550701 Hs3st3b1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1550701 Hs3st3b1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1550701 Hs3st3b1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1550701 Hs3st3b1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 1550701 Hs3st3b1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20201022 MGI 1550701 Hs3st3b1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20200310 MGI PMID:29208648 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20200310 MGI PMID:29208648 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:29208648 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200310 MGI PMID:29208648 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:29208648 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0008957 abnormal placenta junctional zone morphology IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29208648 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0011525 abnormal placenta intervillous maternal lacunae morphology IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0013247 placenta necrosis IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550707 Colgalt1 collagen beta(1-O)galactosyltransferase 1 gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20210506 MGI PMID:31759980 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:19139386 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:11907072 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11907072 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17296171 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20210617 MGI PMID:19139386 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:14688366 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19139386 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11907072 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:14688366 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:19139386 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20210617 MGI PMID:19139386 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11907072 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:11907072 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11907072 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:11907072 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0008817 hematoma IAGP N RGD:5509061 20141003 MGI PMID:19139386 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11907072 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19139386 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0010574 dilated aorta IAGP N RGD:5509061 20141003 MGI PMID:19139386 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0010658 thoracic aorta aneurysm IAGP N RGD:5509061 20141003 MGI PMID:19139386 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:17296171 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0020925 increased susceptibility to Hepadnaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:11907072 1550709 Cxcl10 C-X-C motif chemokine ligand 10 gene MP:0031274 increased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:19139386 1550710 Cntfr ciliary neurotrophic factor receptor gene MP:0000910 small facial motor nucleus IAGP N RGD:5509061 20141003 MGI PMID:7585948 1550710 Cntfr ciliary neurotrophic factor receptor gene MP:0000912 small trigeminal motor nucleus IAGP N RGD:5509061 20141003 MGI PMID:7585948 1550710 Cntfr ciliary neurotrophic factor receptor gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:7585948 1550710 Cntfr ciliary neurotrophic factor receptor gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:18588528 1550710 Cntfr ciliary neurotrophic factor receptor gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:7585948 1550710 Cntfr ciliary neurotrophic factor receptor gene MP:0001435 absent suckling reflex IAGP N RGD:5509061 20141003 MGI PMID:7585948 1550710 Cntfr ciliary neurotrophic factor receptor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7585948 1550710 Cntfr ciliary neurotrophic factor receptor gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18588528 1550710 Cntfr ciliary neurotrophic factor receptor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550713 Ufm1 ubiquitin-fold modifier 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20200310 MGI PMID:27545674 1550713 Ufm1 ubiquitin-fold modifier 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20200310 MGI PMID:27545674 1550713 Ufm1 ubiquitin-fold modifier 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:27545674 1550713 Ufm1 ubiquitin-fold modifier 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:27545674 1550713 Ufm1 ubiquitin-fold modifier 1 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20200310 MGI PMID:27545674 1550713 Ufm1 ubiquitin-fold modifier 1 gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20200310 MGI PMID:27545674 1550713 Ufm1 ubiquitin-fold modifier 1 gene MP:0020069 decreased neocortex size IAGP N RGD:5509061 20200310 MGI PMID:27545674 1550713 Ufm1 ubiquitin-fold modifier 1 gene MP:0020527 small thalamus IAGP N RGD:5509061 20200310 MGI PMID:27545674 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:17916558 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20829355 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0001573 abnormal circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20829355 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:17916558 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17916558 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20709796 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:17916558 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17916558 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:18669605 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0003505 increased prolactinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20709796 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17916558 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0004004 patent ductus venosus IAGP N RGD:5509061 20141003 MGI PMID:18669605 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0004004 patent ductus venosus IAGP N RGD:5509061 20141003 MGI PMID:20829355 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0008816 petechiae IAGP N RGD:5509061 20141003 MGI PMID:17916558 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20829355 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0009078 adrenal gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20709796 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0010128 hypovolemia IAGP N RGD:5509061 20141003 MGI PMID:17916558 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17916558 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20709796 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17916558 1550715 Aip aryl-hydrocarbon receptor-interacting protein gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17916558 1550717 Chmp5 charged multivesicular body protein 5 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:16567502 1550717 Chmp5 charged multivesicular body protein 5 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20200310 MGI PMID:16567502 1550717 Chmp5 charged multivesicular body protein 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:16567502 1550717 Chmp5 charged multivesicular body protein 5 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20200310 MGI PMID:16567502 1550717 Chmp5 charged multivesicular body protein 5 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20200310 MGI PMID:16567502 1550717 Chmp5 charged multivesicular body protein 5 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:16567502 1550717 Chmp5 charged multivesicular body protein 5 gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20200310 MGI PMID:16567502 1550717 Chmp5 charged multivesicular body protein 5 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20200310 MGI PMID:16567502 1550717 Chmp5 charged multivesicular body protein 5 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:16567502 1550717 Chmp5 charged multivesicular body protein 5 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20200310 MGI PMID:16567502 1550717 Chmp5 charged multivesicular body protein 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16567502 1550717 Chmp5 charged multivesicular body protein 5 gene MP:0014239 abnormal intracellular organelle morphology IAGP N RGD:5509061 20230615 MGI PMID:16567502 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:11158324 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20240523 MGI 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20200310 MGI PMID:30046000 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20200310 MGI PMID:12808453 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:11158324 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:12808453 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0000599 enlarged liver IAGP N RGD:5509061 20200310 MGI PMID:11158324 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:11158324 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:12808453 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0000608 dissociated hepatocytes IAGP N RGD:5509061 20200310 MGI PMID:12808453 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0001262 decreased body weight IEA N RGD:5509061 20210826 MGI 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:11158324 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0001426 polydipsia IAGP N RGD:5509061 20200310 MGI PMID:30046000 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:7958910 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20200310 MGI PMID:7958910 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20200310 MGI PMID:7958910 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20200310 MGI PMID:7958910 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:9825865 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20200310 MGI PMID:30046000 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0001762 polyuria IAGP N RGD:5509061 20200310 MGI PMID:30046000 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:11158324 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:7958910 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:7958910 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200310 MGI PMID:16498401 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:30046000 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:11857799 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15282747 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:16498401 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20200310 MGI PMID:7958910 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20200310 MGI PMID:16498401 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200310 MGI PMID:16498401 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:11158324 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:16498401 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:16498401 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:16377800 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20200310 MGI 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20200310 MGI PMID:30046000 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0002989 small kidney IAGP N RGD:5509061 20200310 MGI PMID:30046000 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0003087 absent allantois IAGP N RGD:5509061 20200310 MGI PMID:7958910 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20200310 MGI PMID:30046000 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20200310 MGI PMID:16377800 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0003895 increased ectoderm apoptosis IAGP N RGD:5509061 20200310 MGI PMID:7958910 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:7958910 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0004119 hypokalemia IAGP N RGD:5509061 20200310 MGI PMID:16498401 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20200310 MGI PMID:16498401 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:30046000 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0005030 absent amnion IAGP N RGD:5509061 20200310 MGI PMID:7958910 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:11158324 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:16498401 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20230720 MGI 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:16377800 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:16498401 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20200310 MGI PMID:16498401 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0005355 enlarged thyroid gland IEA N RGD:5509061 20210128 MGI 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0009593 absent chorion IAGP N RGD:5509061 20200310 MGI PMID:7958910 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20200310 MGI 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20200310 MGI PMID:12808453 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16498401 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:7958910 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11158324 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20210128 MGI 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0012105 delayed gastrulation IAGP N RGD:5509061 20200310 MGI PMID:7958910 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0012131 small visceral yolk sac IAGP N RGD:5509061 20200310 MGI PMID:7958910 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:9825865 1550718 Hnf4a hepatic nuclear factor 4, alpha gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:11158324 1550719 Dars2 aspartyl-tRNA synthetase 2 (mitochondrial) gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20211021 MGI 1550719 Dars2 aspartyl-tRNA synthetase 2 (mitochondrial) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550720 Adgrl1 adhesion G protein-coupled receptor L1 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:11741895 1550720 Adgrl1 adhesion G protein-coupled receptor L1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:11741895 1550720 Adgrl1 adhesion G protein-coupled receptor L1 gene MP:0004494 abnormal synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:11741895 1550720 Adgrl1 adhesion G protein-coupled receptor L1 gene MP:0004495 decreased synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:11741895 1550721 Cox6b2 cytochrome c oxidase subunit 6B2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20241107 MGI PMID:37423748 1550721 Cox6b2 cytochrome c oxidase subunit 6B2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20241107 MGI PMID:37423748 1550721 Cox6b2 cytochrome c oxidase subunit 6B2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20241107 MGI PMID:37423748 1550721 Cox6b2 cytochrome c oxidase subunit 6B2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 1550721 Cox6b2 cytochrome c oxidase subunit 6B2 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20241107 MGI PMID:37423748 1550725 Fgf15 fibroblast growth factor 15 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1550725 Fgf15 fibroblast growth factor 15 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20170105 MGI 1550725 Fgf15 fibroblast growth factor 15 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1550725 Fgf15 fibroblast growth factor 15 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20190808 MGI 1550725 Fgf15 fibroblast growth factor 15 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20190808 MGI 1550725 Fgf15 fibroblast growth factor 15 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20170105 MGI 1550725 Fgf15 fibroblast growth factor 15 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0010241 abnormal aortic arch development IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550725 Fgf15 fibroblast growth factor 15 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0012749 decreased cardiac neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550725 Fgf15 fibroblast growth factor 15 gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:15789410 1550726 Micu2 mitochondrial calcium uptake 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20200310 MGI PMID:29073106 1550726 Micu2 mitochondrial calcium uptake 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:29073106 1550726 Micu2 mitochondrial calcium uptake 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20200310 MGI 1550726 Micu2 mitochondrial calcium uptake 2 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20200310 MGI PMID:29073106 1550726 Micu2 mitochondrial calcium uptake 2 gene MP:0008726 increased heart left atrium size IAGP N RGD:5509061 20200310 MGI PMID:29073106 1550726 Micu2 mitochondrial calcium uptake 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:29073106 1550726 Micu2 mitochondrial calcium uptake 2 gene MP:0009870 abnormal abdominal aorta morphology IAGP N RGD:5509061 20200310 MGI PMID:29073106 1550726 Micu2 mitochondrial calcium uptake 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210520 MGI 1550726 Micu2 mitochondrial calcium uptake 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20200310 MGI 1550726 Micu2 mitochondrial calcium uptake 2 gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20200310 MGI PMID:29073106 1550726 Micu2 mitochondrial calcium uptake 2 gene MP:0012557 decreased calcium uptake by cardiac muscle IAGP N RGD:5509061 20200310 MGI PMID:29073106 1550726 Micu2 mitochondrial calcium uptake 2 gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:29073106 1550726 Micu2 mitochondrial calcium uptake 2 gene MP:0020419 decreased cardiac muscle relaxation IAGP N RGD:5509061 20200310 MGI PMID:29073106 1550726 Micu2 mitochondrial calcium uptake 2 gene MP:0031274 increased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:29073106 1550727 Acbd3 acyl-Coenzyme A binding domain containing 3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20170105 MGI 1550727 Acbd3 acyl-Coenzyme A binding domain containing 3 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1550727 Acbd3 acyl-Coenzyme A binding domain containing 3 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160421 MGI 1550727 Acbd3 acyl-Coenzyme A binding domain containing 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1550727 Acbd3 acyl-Coenzyme A binding domain containing 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550733 Otof otoferlin gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17329413 1550733 Otof otoferlin gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:16024820 1550733 Otof otoferlin gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:17055430 1550733 Otof otoferlin gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:17967520 1550733 Otof otoferlin gene MP:0002918 abnormal paired-pulse facilitation IAGP N RGD:5509061 20191226 MGI PMID:25253474 1550733 Otof otoferlin gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20191226 MGI PMID:25253474 1550733 Otof otoferlin gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17055430 1550733 Otof otoferlin gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17055430 1550733 Otof otoferlin gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21451027 1550733 Otof otoferlin gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:17329413 1550733 Otof otoferlin gene MP:0004562 abnormal inner hair cell synaptic ribbon morphology IAGP N RGD:5509061 20141003 MGI PMID:17055430 1550733 Otof otoferlin gene MP:0004716 abnormal cochlear nerve morphology IAGP N RGD:5509061 20191226 MGI PMID:25253474 1550733 Otof otoferlin gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21451027 1550733 Otof otoferlin gene MP:0006335 abnormal hearing electrophysiology IAGP N RGD:5509061 20191226 MGI PMID:25253474 1550733 Otof otoferlin gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:17967520 1550733 Otof otoferlin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17055430 1550733 Otof otoferlin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17329413 1550733 Otof otoferlin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17967520 1550733 Otof otoferlin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21451027 1550733 Otof otoferlin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20191226 MGI PMID:25253474 1550733 Otof otoferlin gene MP:0012486 decreased cochlear VIII nucleus size IAGP N RGD:5509061 20191226 MGI PMID:25253474 1550737 Agpat5 1-acylglycerol-3-phosphate O-acyltransferase 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1550737 Agpat5 1-acylglycerol-3-phosphate O-acyltransferase 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1550737 Agpat5 1-acylglycerol-3-phosphate O-acyltransferase 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1550737 Agpat5 1-acylglycerol-3-phosphate O-acyltransferase 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1550737 Agpat5 1-acylglycerol-3-phosphate O-acyltransferase 5 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1550737 Agpat5 1-acylglycerol-3-phosphate O-acyltransferase 5 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1550737 Agpat5 1-acylglycerol-3-phosphate O-acyltransferase 5 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20230119 MGI 1550737 Agpat5 1-acylglycerol-3-phosphate O-acyltransferase 5 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230119 MGI 1550737 Agpat5 1-acylglycerol-3-phosphate O-acyltransferase 5 gene MP:0002628 hepatic steatosis IEA N RGD:5509061 20200310 MGI 1550737 Agpat5 1-acylglycerol-3-phosphate O-acyltransferase 5 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230119 MGI 1550738 Srr serine racemase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1550738 Srr serine racemase gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1550738 Srr serine racemase gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1550738 Srr serine racemase gene MP:0001147 small testis IEA N RGD:5509061 20230119 MGI 1550738 Srr serine racemase gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1550738 Srr serine racemase gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:19483194 1550738 Srr serine racemase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19065142 1550738 Srr serine racemase gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19065142 1550738 Srr serine racemase gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:19065142 1550738 Srr serine racemase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1550738 Srr serine racemase gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1550738 Srr serine racemase gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:19118183 1550738 Srr serine racemase gene MP:0002463 abnormal neutrophil physiology IEA N RGD:5509061 20150625 MGI 1550738 Srr serine racemase gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:19065142 1550738 Srr serine racemase gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1550738 Srr serine racemase gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:19065142 1550738 Srr serine racemase gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19065142 1550738 Srr serine racemase gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:19065142 1550738 Srr serine racemase gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:19118183 1550738 Srr serine racemase gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:19483194 1550738 Srr serine racemase gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:19065142 1550738 Srr serine racemase gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:19483194 1550738 Srr serine racemase gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19483194 1550738 Srr serine racemase gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:19483194 1550738 Srr serine racemase gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:19065142 1550738 Srr serine racemase gene MP:0030691 increased serine level IAGP N RGD:5509061 20180927 MGI PMID:19483194 1550738 Srr serine racemase gene MP:0030692 decreased serine level IAGP N RGD:5509061 20180927 MGI PMID:19118183 1550738 Srr serine racemase gene MP:0030692 decreased serine level IAGP N RGD:5509061 20180927 MGI PMID:19483194 1550740 Qars1 glutaminyl-tRNA synthetase 1 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20231207 MGI 1550740 Qars1 glutaminyl-tRNA synthetase 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20231207 MGI 1550740 Qars1 glutaminyl-tRNA synthetase 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20231207 MGI 1550740 Qars1 glutaminyl-tRNA synthetase 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 1550740 Qars1 glutaminyl-tRNA synthetase 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1550740 Qars1 glutaminyl-tRNA synthetase 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 1550740 Qars1 glutaminyl-tRNA synthetase 1 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20231207 MGI 1550740 Qars1 glutaminyl-tRNA synthetase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1550740 Qars1 glutaminyl-tRNA synthetase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20231207 MGI 1550743 Tmx2 thioredoxin-related transmembrane protein 2 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20240926 MGI 1550743 Tmx2 thioredoxin-related transmembrane protein 2 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20191128 MGI 1550743 Tmx2 thioredoxin-related transmembrane protein 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20191128 MGI 1550743 Tmx2 thioredoxin-related transmembrane protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550743 Tmx2 thioredoxin-related transmembrane protein 2 gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20191128 MGI 1550743 Tmx2 thioredoxin-related transmembrane protein 2 gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20191128 MGI 1550743 Tmx2 thioredoxin-related transmembrane protein 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1550744 Noa1 nitric oxide associated 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21118999 1550744 Noa1 nitric oxide associated 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21118999 1550744 Noa1 nitric oxide associated 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21118999 1550744 Noa1 nitric oxide associated 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:21118999 1550744 Noa1 nitric oxide associated 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:21118999 1550744 Noa1 nitric oxide associated 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21118999 1550744 Noa1 nitric oxide associated 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:21118999 1550744 Noa1 nitric oxide associated 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:21118999 1550744 Noa1 nitric oxide associated 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21118999 1550744 Noa1 nitric oxide associated 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:21118999 1550744 Noa1 nitric oxide associated 1 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:21118999 1550744 Noa1 nitric oxide associated 1 gene MP:0013505 decreased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:21118999 1550745 Hdgfl1 HDGF like 1 gene MP:0001147 small testis IEA N RGD:5509061 20200310 MGI 1550745 Hdgfl1 HDGF like 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1550745 Hdgfl1 HDGF like 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201022 MGI PMID:32588039 1550745 Hdgfl1 HDGF like 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1550745 Hdgfl1 HDGF like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200310 MGI 1550745 Hdgfl1 HDGF like 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1550745 Hdgfl1 HDGF like 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1550746 Bzw1 basic leucine zipper and W2 domains 1 gene MP:0001304 cataract IEA N RGD:5509061 20190502 MGI 1550746 Bzw1 basic leucine zipper and W2 domains 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1550746 Bzw1 basic leucine zipper and W2 domains 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1550746 Bzw1 basic leucine zipper and W2 domains 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1550747 Gatad2a GATA zinc finger domain containing 2A gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20200310 MGI PMID:17565372 1550747 Gatad2a GATA zinc finger domain containing 2A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:17565372 1550747 Gatad2a GATA zinc finger domain containing 2A gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20200310 MGI PMID:17565372 1550747 Gatad2a GATA zinc finger domain containing 2A gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:17565372 1550747 Gatad2a GATA zinc finger domain containing 2A gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:17565372 1550747 Gatad2a GATA zinc finger domain containing 2A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17565372 1550747 Gatad2a GATA zinc finger domain containing 2A gene MP:0011256 abnormal neural fold morphology IAGP N RGD:5509061 20200310 MGI PMID:17565372 1550748 Mrpl47 mitochondrial ribosomal protein L47 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550748 Mrpl47 mitochondrial ribosomal protein L47 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1550748 Mrpl47 mitochondrial ribosomal protein L47 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1550749 Efcab2 EF-hand calcium binding domain 2 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1550752 L2hgdh L-2-hydroxyglutarate dehydrogenase gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:25763823 1550752 L2hgdh L-2-hydroxyglutarate dehydrogenase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1550752 L2hgdh L-2-hydroxyglutarate dehydrogenase gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1550752 L2hgdh L-2-hydroxyglutarate dehydrogenase gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220519 MGI 1550752 L2hgdh L-2-hydroxyglutarate dehydrogenase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:25763823 1550752 L2hgdh L-2-hydroxyglutarate dehydrogenase gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20200310 MGI PMID:25763823 1550752 L2hgdh L-2-hydroxyglutarate dehydrogenase gene MP:0002899 fatigue IAGP N RGD:5509061 20200310 MGI PMID:25763823 1550752 L2hgdh L-2-hydroxyglutarate dehydrogenase gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20200310 MGI PMID:25763823 1550752 L2hgdh L-2-hydroxyglutarate dehydrogenase gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:25763823 1550752 L2hgdh L-2-hydroxyglutarate dehydrogenase gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20200310 MGI PMID:25763823 1550752 L2hgdh L-2-hydroxyglutarate dehydrogenase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20200310 MGI PMID:25763823 1550752 L2hgdh L-2-hydroxyglutarate dehydrogenase gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20200310 MGI PMID:25763823 1550752 L2hgdh L-2-hydroxyglutarate dehydrogenase gene MP:0011617 abnormal habituation IAGP N RGD:5509061 20200310 MGI PMID:25763823 1550752 L2hgdh L-2-hydroxyglutarate dehydrogenase gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200310 MGI PMID:25763823 1550752 L2hgdh L-2-hydroxyglutarate dehydrogenase gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:25763823 1550753 Luc7l Luc7-like gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1550753 Luc7l Luc7-like gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1550753 Luc7l Luc7-like gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1550753 Luc7l Luc7-like gene MP:0000599 enlarged liver IEA N RGD:5509061 20210520 MGI 1550753 Luc7l Luc7-like gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1550753 Luc7l Luc7-like gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1550753 Luc7l Luc7-like gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1550753 Luc7l Luc7-like gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1550753 Luc7l Luc7-like gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1550753 Luc7l Luc7-like gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1550753 Luc7l Luc7-like gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 1550753 Luc7l Luc7-like gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1550753 Luc7l Luc7-like gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1550753 Luc7l Luc7-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15474286 1550753 Luc7l Luc7-like gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1550753 Luc7l Luc7-like gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1550753 Luc7l Luc7-like gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1550753 Luc7l Luc7-like gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210826 MGI 1550753 Luc7l Luc7-like gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1550754 Slc38a5 solute carrier family 38, member 5 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20180322 MGI PMID:28591637 1550754 Slc38a5 solute carrier family 38, member 5 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20180322 MGI PMID:28591637 1550754 Slc38a5 solute carrier family 38, member 5 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180322 MGI PMID:28591637 1550754 Slc38a5 solute carrier family 38, member 5 gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20180322 MGI PMID:28591637 1550754 Slc38a5 solute carrier family 38, member 5 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20180322 MGI PMID:28591637 1550754 Slc38a5 solute carrier family 38, member 5 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20180322 MGI PMID:28591637 1550755 Akap9 A kinase anchor protein 9 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20160804 MGI 1550755 Akap9 A kinase anchor protein 9 gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20160804 MGI 1550755 Akap9 A kinase anchor protein 9 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12855593 1550755 Akap9 A kinase anchor protein 9 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23608191 1550755 Akap9 A kinase anchor protein 9 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23608191 1550755 Akap9 A kinase anchor protein 9 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12855593 1550755 Akap9 A kinase anchor protein 9 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23608191 1550755 Akap9 A kinase anchor protein 9 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0002216 abnormal seminiferous tubule morphology IEA N RGD:5509061 20141003 MGI 1550755 Akap9 A kinase anchor protein 9 gene MP:0002686 globozoospermia IEA N RGD:5509061 20141003 MGI 1550755 Akap9 A kinase anchor protein 9 gene MP:0002687 oligozoospermia IEA N RGD:5509061 20141003 MGI 1550755 Akap9 A kinase anchor protein 9 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20141003 MGI PMID:23608191 1550755 Akap9 A kinase anchor protein 9 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20160804 MGI 1550755 Akap9 A kinase anchor protein 9 gene MP:0004852 decreased testis weight IEA N RGD:5509061 20141003 MGI 1550755 Akap9 A kinase anchor protein 9 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0004910 decreased seminal vesicle weight IEA N RGD:5509061 20141003 MGI 1550755 Akap9 A kinase anchor protein 9 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:23608191 1550755 Akap9 A kinase anchor protein 9 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23608191 1550755 Akap9 A kinase anchor protein 9 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12855593 1550755 Akap9 A kinase anchor protein 9 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20160804 MGI 1550755 Akap9 A kinase anchor protein 9 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20160804 MGI 1550755 Akap9 A kinase anchor protein 9 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20160922 MGI PMID:24652767 1550755 Akap9 A kinase anchor protein 9 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:14779004 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15871460 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16026577 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000380 small hair follicles IAGP N RGD:5509061 20181129 MGI PMID:16026577 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:15871460 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20181129 MGI PMID:15240817 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000389 disorganized outer root sheath cells IAGP N RGD:5509061 20141003 MGI PMID:15240817 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000392 accelerated hair follicle regression IAGP N RGD:5509061 20141003 MGI PMID:16026577 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000392 accelerated hair follicle regression IAGP N RGD:5509061 20141003 MGI PMID:16103225 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:14779004 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:15240817 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:17914447 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16026577 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:15240817 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:16026577 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:16103225 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:17914447 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:15871460 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:16103225 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:16026577 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:16103225 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0001211 wrinkled skin IEA N RGD:5509061 20111116 MGI 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:4618567 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:16026577 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:15240817 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:16026577 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0001278 kinked vibrissae IAGP N RGD:5509061 20141003 MGI PMID:16103225 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0001279 wavy vibrissae IAGP N RGD:5509061 20141003 MGI PMID:14779004 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0001279 wavy vibrissae IAGP N RGD:5509061 20141003 MGI PMID:15871460 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0001279 wavy vibrissae IAGP N RGD:5509061 20141003 MGI PMID:17914447 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:15871460 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:15240817 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20191031 MGI PMID:15971077 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16026577 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:15240817 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:16103225 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20141003 MGI PMID:14779004 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20141003 MGI 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:15871460 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:16026577 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20181129 MGI PMID:15240817 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:15240817 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:15871460 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:16026577 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:16103225 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20141003 MGI PMID:16026577 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20141003 MGI PMID:16103225 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003812 abnormal hair medulla IAGP N RGD:5509061 20141003 MGI PMID:15871460 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003812 abnormal hair medulla IAGP N RGD:5509061 20141003 MGI PMID:16026577 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003812 abnormal hair medulla IAGP N RGD:5509061 20141003 MGI PMID:16103225 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003813 abnormal hair follicle dermal papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:15871460 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003813 abnormal hair follicle dermal papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:16103225 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20191031 MGI PMID:15971077 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20191031 MGI PMID:15971077 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:6696991 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0008860 abnormal hair cycle telogen phase IAGP N RGD:5509061 20181129 MGI PMID:16026577 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0009351 thin hair shaft IAGP N RGD:5509061 20141003 MGI PMID:16026577 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0009351 thin hair shaft IAGP N RGD:5509061 20141003 MGI PMID:16103225 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:15240817 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0010686 abnormal hair follicle matrix region morphology IAGP N RGD:5509061 20181129 MGI PMID:15871460 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0010686 abnormal hair follicle matrix region morphology IAGP N RGD:5509061 20181129 MGI PMID:16103225 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0010690 thick hair follicle outer root sheath IAGP N RGD:5509061 20141003 MGI PMID:15871460 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0010693 thin hair follicle inner root sheath IAGP N RGD:5509061 20141003 MGI PMID:15871460 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0011195 increased hair follicle apoptosis IAGP N RGD:5509061 20181129 MGI PMID:16103225 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0011939 increased food intake IAGP N RGD:5509061 20191031 MGI PMID:15971077 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0011978 abnormal potassium ion homeostasis IAGP N RGD:5509061 20191031 MGI PMID:15971077 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20191031 MGI PMID:15971077 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0013759 decreased intestinal glucose absorption IAGP N RGD:5509061 20191031 MGI PMID:15971077 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0030575 decreased hair follicle cell proliferation IAGP N RGD:5509061 20181129 MGI PMID:16103225 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0030920 small hair follicle bulb IAGP N RGD:5509061 20181220 MGI PMID:15871460 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0030920 small hair follicle bulb IAGP N RGD:5509061 20181220 MGI PMID:16103225 1550757 Sgk3 serum/glucocorticoid regulated kinase 3 gene MP:0030925 early exit from anagen phase IEA N RGD:5509061 20181220 MGI 1550758 Tmem45b transmembrane protein 45b gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20221215 MGI PMID:36322717 1550758 Tmem45b transmembrane protein 45b gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20221215 MGI PMID:36322717 1550759 Hdac4 histone deacetylase 4 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15537544 1550759 Hdac4 histone deacetylase 4 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15537544 1550759 Hdac4 histone deacetylase 4 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:15537544 1550759 Hdac4 histone deacetylase 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15537544 1550759 Hdac4 histone deacetylase 4 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:19672313 1550759 Hdac4 histone deacetylase 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19672313 1550759 Hdac4 histone deacetylase 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15537544 1550759 Hdac4 histone deacetylase 4 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200723 MGI PMID:27884425 1550759 Hdac4 histone deacetylase 4 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200723 MGI PMID:32153359 1550759 Hdac4 histone deacetylase 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200723 MGI PMID:32153359 1550759 Hdac4 histone deacetylase 4 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1550759 Hdac4 histone deacetylase 4 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20200723 MGI PMID:32153359 1550759 Hdac4 histone deacetylase 4 gene MP:0001432 abnormal food preference IAGP N RGD:5509061 20200723 MGI PMID:27884425 1550759 Hdac4 histone deacetylase 4 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20200723 MGI PMID:27884425 1550759 Hdac4 histone deacetylase 4 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20200723 MGI PMID:32153359 1550759 Hdac4 histone deacetylase 4 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:19672313 1550759 Hdac4 histone deacetylase 4 gene MP:0001994 increased blinking frequency IAGP N RGD:5509061 20141003 MGI PMID:19672313 1550759 Hdac4 histone deacetylase 4 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20200723 MGI PMID:32153359 1550759 Hdac4 histone deacetylase 4 gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20200723 MGI PMID:27884425 1550759 Hdac4 histone deacetylase 4 gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20200723 MGI PMID:32153359 1550759 Hdac4 histone deacetylase 4 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19672313 1550759 Hdac4 histone deacetylase 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1550759 Hdac4 histone deacetylase 4 gene MP:0003063 increased coping response IAGP N RGD:5509061 20200723 MGI PMID:27884425 1550759 Hdac4 histone deacetylase 4 gene MP:0003417 premature endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15537544 1550759 Hdac4 histone deacetylase 4 gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:19672313 1550759 Hdac4 histone deacetylase 4 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20200723 MGI PMID:32153359 1550759 Hdac4 histone deacetylase 4 gene MP:0004243 abnormal motor nerve collateral sprouting IAGP N RGD:5509061 20141003 MGI PMID:20007902 1550759 Hdac4 histone deacetylase 4 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20200723 MGI PMID:27884425 1550759 Hdac4 histone deacetylase 4 gene MP:0006432 abnormal costal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15537544 1550759 Hdac4 histone deacetylase 4 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20211021 MGI 1550759 Hdac4 histone deacetylase 4 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15537544 1550759 Hdac4 histone deacetylase 4 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:19672313 1550759 Hdac4 histone deacetylase 4 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:19672313 1550759 Hdac4 histone deacetylase 4 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:17786239 1550759 Hdac4 histone deacetylase 4 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20200723 MGI PMID:32153359 1550759 Hdac4 histone deacetylase 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15537544 1550759 Hdac4 histone deacetylase 4 gene MP:0011939 increased food intake IAGP N RGD:5509061 20200723 MGI PMID:27884425 1550759 Hdac4 histone deacetylase 4 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20200723 MGI PMID:32153359 1550759 Hdac4 histone deacetylase 4 gene MP:0030356 premature lambdoid suture closure IAGP N RGD:5509061 20171207 MGI PMID:15537544 1550759 Hdac4 histone deacetylase 4 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:19672313 1550760 Thap4 THAP domain containing 4 gene MP:0001147 small testis IAGP N RGD:5509061 20240801 MGI PMID:38658415 1550760 Thap4 THAP domain containing 4 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20240801 MGI PMID:38658415 1550760 Thap4 THAP domain containing 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240801 MGI PMID:38658415 1550760 Thap4 THAP domain containing 4 gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20240801 MGI PMID:38658415 1550761 Ccl4 C-C motif chemokine ligand 4 gene MP:0000550 abnormal forelimb morphology IEA N RGD:5509061 20240523 MGI 1550761 Ccl4 C-C motif chemokine ligand 4 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20240502 MGI PMID:36863097 1550761 Ccl4 C-C motif chemokine ligand 4 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20240509 MGI PMID:36863097 1550761 Ccl4 C-C motif chemokine ligand 4 gene MP:0012000 abnormal limb position IEA N RGD:5509061 20240523 MGI 1550764 Jmjd4 jumonji domain containing 4 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1550764 Jmjd4 jumonji domain containing 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:27147518 1550764 Jmjd4 jumonji domain containing 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1550764 Jmjd4 jumonji domain containing 4 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 1550764 Jmjd4 jumonji domain containing 4 gene MP:0005358 abnormal incisor morphology IEA N RGD:5509061 20210128 MGI 1550764 Jmjd4 jumonji domain containing 4 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1550764 Jmjd4 jumonji domain containing 4 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 1550764 Jmjd4 jumonji domain containing 4 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1550764 Jmjd4 jumonji domain containing 4 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210520 MGI 1550770 Syap1 synapse associated protein 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190725 MGI PMID:31118165 1550770 Syap1 synapse associated protein 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190725 MGI PMID:31118165 1550770 Syap1 synapse associated protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:27344443 1550770 Syap1 synapse associated protein 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20190725 MGI PMID:31118165 1550772 Slc1a5 solute carrier family 1 (neutral amino acid transporter), member 5 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20180215 MGI PMID:24792914 1550772 Slc1a5 solute carrier family 1 (neutral amino acid transporter), member 5 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180215 MGI PMID:24792914 1550772 Slc1a5 solute carrier family 1 (neutral amino acid transporter), member 5 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180215 MGI PMID:24792914 1550772 Slc1a5 solute carrier family 1 (neutral amino acid transporter), member 5 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180215 MGI PMID:24792914 1550772 Slc1a5 solute carrier family 1 (neutral amino acid transporter), member 5 gene MP:0008087 decreased T helper 1 cell number IAGP N RGD:5509061 20180215 MGI PMID:24792914 1550772 Slc1a5 solute carrier family 1 (neutral amino acid transporter), member 5 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20180215 MGI PMID:24792914 1550772 Slc1a5 solute carrier family 1 (neutral amino acid transporter), member 5 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20180215 MGI PMID:24792914 1550772 Slc1a5 solute carrier family 1 (neutral amino acid transporter), member 5 gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20180215 MGI PMID:24792914 1550772 Slc1a5 solute carrier family 1 (neutral amino acid transporter), member 5 gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20180215 MGI PMID:24792914 1550772 Slc1a5 solute carrier family 1 (neutral amino acid transporter), member 5 gene MP:0010836 decreased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20180215 MGI PMID:24792914 1550773 Srpk3 serine/arginine-rich protein specific kinase 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1550773 Srpk3 serine/arginine-rich protein specific kinase 3 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20220811 MGI 1550773 Srpk3 serine/arginine-rich protein specific kinase 3 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20181227 MGI 1550773 Srpk3 serine/arginine-rich protein specific kinase 3 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16140986 1550773 Srpk3 serine/arginine-rich protein specific kinase 3 gene MP:0002731 megacolon IEA N RGD:5509061 20181227 MGI 1550773 Srpk3 serine/arginine-rich protein specific kinase 3 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:16140986 1550773 Srpk3 serine/arginine-rich protein specific kinase 3 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:16140986 1550773 Srpk3 serine/arginine-rich protein specific kinase 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1550774 Drosha drosha, ribonuclease type III gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0000380 small hair follicles IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0000410 waved hair IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0000414 alopecia IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0000520 absent kidney IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0001192 scaly skin IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:23918385 1550774 Drosha drosha, ribonuclease type III gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0001575 cyanosis IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0001863 blood vessel inflammation IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0001954 respiratory distress IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:23918385 1550774 Drosha drosha, ribonuclease type III gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0003853 dry skin IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0003875 abnormal hair follicle regression IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0004941 abnormal regulatory T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0005150 cachexia IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0008559 abnormal interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0008698 abnormal interleukin-4 secretion IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550774 Drosha drosha, ribonuclease type III gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0009759 abnormal hair follicle bulge morphology IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20200310 MGI PMID:22434867 1550774 Drosha drosha, ribonuclease type III gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23918385 1550774 Drosha drosha, ribonuclease type III gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0011940 decreased food intake IAGP N RGD:5509061 20220331 MGI PMID:30367465 1550774 Drosha drosha, ribonuclease type III gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20200310 MGI PMID:18725527 1550775 Atp8b3 ATPase, class I, type 8B, member 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:14975727 1550775 Atp8b3 ATPase, class I, type 8B, member 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:14975727 1550775 Atp8b3 ATPase, class I, type 8B, member 3 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:14975727 1550775 Atp8b3 ATPase, class I, type 8B, member 3 gene MP:0005410 abnormal fertilization IAGP N RGD:5509061 20141003 MGI PMID:14975727 1550775 Atp8b3 ATPase, class I, type 8B, member 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1550776 Fcgr4 Fc receptor, IgG, low affinity IV gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:23754379 1550776 Fcgr4 Fc receptor, IgG, low affinity IV gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20974962 1550776 Fcgr4 Fc receptor, IgG, low affinity IV gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:23754379 1550776 Fcgr4 Fc receptor, IgG, low affinity IV gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:23754379 1550776 Fcgr4 Fc receptor, IgG, low affinity IV gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:20974962 1550776 Fcgr4 Fc receptor, IgG, low affinity IV gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:23754379 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0000436 abnormal head movements IAGP N RGD:5509061 20200310 MGI PMID:8706126 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:8706126 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:8917582 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20200310 MGI PMID:8706126 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20200310 MGI PMID:8917582 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0000756 forelimb paralysis IAGP N RGD:5509061 20200310 MGI PMID:8917582 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20200310 MGI PMID:16551741 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20200310 MGI PMID:18987190 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20200310 MGI PMID:9464989 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0000921 demyelination IAGP N RGD:5509061 20200310 MGI PMID:8917582 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0000921 demyelination IAGP N RGD:5509061 20200310 MGI PMID:9560463 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:8706126 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:8706126 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:8917582 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:18987190 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:8917582 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20200310 MGI PMID:8706126 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20200310 MGI PMID:8917582 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:8917582 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:8706126 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:8917582 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20200310 MGI PMID:18987190 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20200310 MGI PMID:10601330 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20200310 MGI PMID:8917582 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20200310 MGI PMID:9464989 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20200310 MGI PMID:18987190 1550779 Ugt8a UDP galactosyltransferase 8A gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:16551741 1550780 Rab9 RAB9, member RAS oncogene family gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1550781 Parp8 poly (ADP-ribose) polymerase family, member 8 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1550781 Parp8 poly (ADP-ribose) polymerase family, member 8 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1550781 Parp8 poly (ADP-ribose) polymerase family, member 8 gene MP:0003064 decreased coping response IEA N RGD:5509061 20210128 MGI 1550782 Abcb8 ATP-binding cassette, sub-family B member 8 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:22375032 1550782 Abcb8 ATP-binding cassette, sub-family B member 8 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22375032 1550782 Abcb8 ATP-binding cassette, sub-family B member 8 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:22375032 1550782 Abcb8 ATP-binding cassette, sub-family B member 8 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:22375032 1550782 Abcb8 ATP-binding cassette, sub-family B member 8 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22375032 1550782 Abcb8 ATP-binding cassette, sub-family B member 8 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:22375032 1550782 Abcb8 ATP-binding cassette, sub-family B member 8 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:22375032 1550782 Abcb8 ATP-binding cassette, sub-family B member 8 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:22375032 1550782 Abcb8 ATP-binding cassette, sub-family B member 8 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22375032 1550782 Abcb8 ATP-binding cassette, sub-family B member 8 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:22375032 1550782 Abcb8 ATP-binding cassette, sub-family B member 8 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:22375032 1550782 Abcb8 ATP-binding cassette, sub-family B member 8 gene MP:0020367 increased heart iron level IAGP N RGD:5509061 20161020 MGI PMID:22375032 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20160609 MGI PMID:26490168 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20160609 MGI PMID:26490168 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20240523 MGI 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20160609 MGI PMID:26490168 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20160609 MGI PMID:26490168 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20160609 MGI PMID:26490168 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0002776 increased Sertoli cell number IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0003582 abnormal ovary development IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20160609 MGI PMID:26490168 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20160609 MGI PMID:26490168 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20160609 MGI PMID:26490168 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20160609 MGI PMID:26490168 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220519 MGI 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20160609 MGI PMID:26490168 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20160609 MGI PMID:26490168 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20160609 MGI PMID:26490168 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0013538 increased Harderian gland adenoma incidence IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0014040 increased cellular sensitivity to DNA damaging agents IAGP N RGD:5509061 20160609 MGI PMID:26637282 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0030934 decreased primordial germ cell proliferation IAGP N RGD:5509061 20190411 MGI PMID:26490168 1550783 Brip1 BRCA1 interacting protein C-terminal helicase 1 gene MP:0030935 increased primordial germ cell apoptosis IAGP N RGD:5509061 20190411 MGI PMID:26490168 1550784 Tbcel tubulin folding cofactor E-like gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20240523 MGI 1550784 Tbcel tubulin folding cofactor E-like gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:22723298 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22723298 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22723298 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22158707 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:22723298 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0004112 abnormal arteriole morphology IAGP N RGD:5509061 20141003 MGI PMID:22723298 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:22723298 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22723298 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22723298 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0011401 abnormal vascular smooth muscle development IAGP N RGD:5509061 20141003 MGI PMID:22723298 1550785 Tmsb4x thymosin, beta 4, X chromosome gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1550795 Dzip1 DAZ interacting protein 1 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20210715 MGI PMID:31118289 1550795 Dzip1 DAZ interacting protein 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:23955340 1550795 Dzip1 DAZ interacting protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23955340 1550795 Dzip1 DAZ interacting protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20230302 MGI PMID:32051257 1550795 Dzip1 DAZ interacting protein 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23955340 1550795 Dzip1 DAZ interacting protein 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230302 MGI PMID:32051257 1550795 Dzip1 DAZ interacting protein 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230302 MGI PMID:32051257 1550795 Dzip1 DAZ interacting protein 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230302 MGI PMID:32051257 1550795 Dzip1 DAZ interacting protein 1 gene MP:0006120 mitral valve prolapse IAGP N RGD:5509061 20210715 MGI PMID:31118289 1550795 Dzip1 DAZ interacting protein 1 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20230302 MGI PMID:32051257 1550795 Dzip1 DAZ interacting protein 1 gene MP:0010614 abnormal mitral valve cusp morphology IAGP N RGD:5509061 20210715 MGI PMID:31118289 1550795 Dzip1 DAZ interacting protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23955340 1550795 Dzip1 DAZ interacting protein 1 gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20210715 MGI PMID:31118289 1550795 Dzip1 DAZ interacting protein 1 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:23955340 1550795 Dzip1 DAZ interacting protein 1 gene MP:0013206 abnormal motile cilium morphology IAGP N RGD:5509061 20210715 MGI PMID:31118289 1550796 Sulf1 sulfatase 1 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17593974 1550796 Sulf1 sulfatase 1 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:17593974 1550796 Sulf1 sulfatase 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22298771 1550796 Sulf1 sulfatase 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17720696 1550796 Sulf1 sulfatase 1 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17720696 1550796 Sulf1 sulfatase 1 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17720696 1550796 Sulf1 sulfatase 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17593974 1550796 Sulf1 sulfatase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16901266 1550796 Sulf1 sulfatase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17593974 1550796 Sulf1 sulfatase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17720696 1550796 Sulf1 sulfatase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17720696 1550796 Sulf1 sulfatase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17720696 1550796 Sulf1 sulfatase 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:17720696 1550796 Sulf1 sulfatase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:16901266 1550796 Sulf1 sulfatase 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20210211 MGI PMID:17720696 1550796 Sulf1 sulfatase 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17593974 1550796 Sulf1 sulfatase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16901266 1550796 Sulf1 sulfatase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17593974 1550796 Sulf1 sulfatase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17720696 1550796 Sulf1 sulfatase 1 gene MP:0002411 decreased susceptibility to bacterial infection IEA N RGD:5509061 20170406 MGI 1550796 Sulf1 sulfatase 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:17593974 1550796 Sulf1 sulfatase 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:17593974 1550796 Sulf1 sulfatase 1 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0004545 enlarged esophagus IAGP N RGD:5509061 20141003 MGI PMID:17720696 1550796 Sulf1 sulfatase 1 gene MP:0004548 dilated esophagus IAGP N RGD:5509061 20141003 MGI PMID:17720696 1550796 Sulf1 sulfatase 1 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0004622 sacral vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0004687 split vertebrae IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0004831 long incisors IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16901266 1550796 Sulf1 sulfatase 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17593974 1550796 Sulf1 sulfatase 1 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:17593974 1550796 Sulf1 sulfatase 1 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:17593974 1550796 Sulf1 sulfatase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17720696 1550796 Sulf1 sulfatase 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17593974 1550796 Sulf1 sulfatase 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:16901266 1550796 Sulf1 sulfatase 1 gene MP:0012279 wide sternum IAGP N RGD:5509061 20141003 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20180125 MGI PMID:18213582 1550796 Sulf1 sulfatase 1 gene MP:0031088 coughing IAGP N RGD:5509061 20210211 MGI PMID:17720696 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0000111 cleft palate IEA N RGD:5509061 20230601 MGI 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:22902753 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20200310 MGI PMID:24680895 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20200310 MGI PMID:22510880 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:22354172 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:25063677 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:26527802 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20200611 MGI PMID:32052574 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:22190642 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:22354172 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:22464327 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:30224759 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20200310 MGI PMID:17934449 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20200310 MGI PMID:24680895 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20200310 MGI PMID:15509778 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20200310 MGI PMID:17934449 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20230601 MGI 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20200310 MGI PMID:15509778 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20200310 MGI PMID:17934449 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:15509778 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:17934449 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20200310 MGI PMID:27736879 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20200310 MGI PMID:15509778 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20200310 MGI PMID:17934449 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21727895 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20220721 MGI PMID:34376666 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22464327 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22895187 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:26527802 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20200310 MGI PMID:22190642 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20200310 MGI PMID:30224759 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20211202 MGI PMID:33431892 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:23726973 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:26527802 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20200310 MGI PMID:22510880 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20200310 MGI PMID:24680895 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20200310 MGI PMID:24680895 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:22902753 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200611 MGI PMID:32052574 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20200310 MGI PMID:22510880 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20200310 MGI PMID:23202126 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20200310 MGI PMID:22354172 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20200310 MGI PMID:30224759 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20200310 MGI PMID:21727895 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:22354172 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:30224759 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:30224759 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20230629 MGI PMID:34240584 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20200310 MGI PMID:15509778 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:23726973 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20200310 MGI PMID:21727895 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20200310 MGI PMID:22190642 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20200310 MGI PMID:22902753 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20200310 MGI PMID:24680895 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0010156 abnormal small intestinal crypt cell physiology IAGP N RGD:5509061 20200310 MGI PMID:26527802 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21727895 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20200310 MGI PMID:24680895 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20200310 MGI PMID:27736879 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0011006 abnormal epidermal stem cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:24680895 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200611 MGI PMID:32052574 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15509778 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17934449 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21927002 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24680895 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24680895 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:24680895 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0012734 abnormal response to radiation IAGP N RGD:5509061 20200310 MGI PMID:30224759 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0013264 tongue ankylosis IAGP N RGD:5509061 20200310 MGI PMID:15509778 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0013481 abnormal ileum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:22902753 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0013485 increased Paneth cell number IAGP N RGD:5509061 20200310 MGI PMID:22190642 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20200310 MGI PMID:27736879 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0013487 abnormal Paneth cell physiology IAGP N RGD:5509061 20200310 MGI PMID:22190642 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0013648 increased CD11b-high dendritic cell number IEA N RGD:5509061 20230601 MGI 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0013886 increased CD4-negative, CD25-positive NK T cell number IEA N RGD:5509061 20230601 MGI 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0013890 increased CD8-positive, CD25-positive alpha-beta T cell number IEA N RGD:5509061 20230601 MGI 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0014076 absent Paneth cells IAGP N RGD:5509061 20200310 MGI PMID:22354172 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0014077 ectopic Paneth cells IAGP N RGD:5509061 20200310 MGI PMID:22510880 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0014077 ectopic Paneth cells IAGP N RGD:5509061 20200310 MGI PMID:22902753 1550798 Lgr5 leucine rich repeat containing G protein coupled receptor 5 gene MP:0014201 abnormal intestinal epithelium physiology IAGP N RGD:5509061 20200409 MGI PMID:30449703 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:28355569 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0000753 paralysis IAGP N RGD:5509061 20200310 MGI PMID:28355569 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20200310 MGI PMID:19805030 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20200310 MGI PMID:28355569 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20200310 MGI PMID:28355569 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20200310 MGI PMID:28355569 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:19805030 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:28355569 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200310 MGI PMID:19805030 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20200310 MGI PMID:28355569 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20200310 MGI PMID:28355569 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200310 MGI PMID:19805030 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20200310 MGI 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20200310 MGI PMID:19805030 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20200310 MGI PMID:28355569 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:28355569 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0010559 heart block IAGP N RGD:5509061 20200310 MGI PMID:28355569 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0010732 abnormal node of Ranvier morphology IAGP N RGD:5509061 20200310 MGI PMID:19805030 1550799 Sh3tc2 SH3 domain and tetratricopeptide repeats 2 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20200310 MGI PMID:28355569 1550801 Rcc2 regulator of chromosome condensation 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1550801 Rcc2 regulator of chromosome condensation 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200310 MGI 1550801 Rcc2 regulator of chromosome condensation 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20200310 MGI 1550801 Rcc2 regulator of chromosome condensation 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 1550801 Rcc2 regulator of chromosome condensation 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1550801 Rcc2 regulator of chromosome condensation 2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 1550801 Rcc2 regulator of chromosome condensation 2 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20201231 MGI 1550802 Sec13 SEC13 homolog, nuclear pore and COPII coat complex component gene MP:0010580 decreased heart left ventricle size IEA N RGD:5509061 20240523 MGI 1550802 Sec13 SEC13 homolog, nuclear pore and COPII coat complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1550804 Actl6b actin-like 6B gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20200310 MGI PMID:17920018 1550804 Actl6b actin-like 6B gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:17920018 1550804 Actl6b actin-like 6B gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1550804 Actl6b actin-like 6B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1550804 Actl6b actin-like 6B gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20200310 MGI PMID:17920018 1550804 Actl6b actin-like 6B gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20200310 MGI PMID:17920018 1550804 Actl6b actin-like 6B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17920018 1550804 Actl6b actin-like 6B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1550806 Dpy30 dpy-30, histone methyltransferase complex regulatory subunit gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20160421 MGI PMID:25805847 1550806 Dpy30 dpy-30, histone methyltransferase complex regulatory subunit gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20160421 MGI PMID:25805847 1550806 Dpy30 dpy-30, histone methyltransferase complex regulatory subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160421 MGI PMID:25805847 1550806 Dpy30 dpy-30, histone methyltransferase complex regulatory subunit gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20160421 MGI PMID:25805847 1550806 Dpy30 dpy-30, histone methyltransferase complex regulatory subunit gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160421 MGI PMID:25805847 1550806 Dpy30 dpy-30, histone methyltransferase complex regulatory subunit gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20160421 MGI PMID:25805847 1550806 Dpy30 dpy-30, histone methyltransferase complex regulatory subunit gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20160421 MGI PMID:25805847 1550806 Dpy30 dpy-30, histone methyltransferase complex regulatory subunit gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1550806 Dpy30 dpy-30, histone methyltransferase complex regulatory subunit gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20160421 MGI PMID:25805847 1550806 Dpy30 dpy-30, histone methyltransferase complex regulatory subunit gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20160421 MGI PMID:25805847 1550806 Dpy30 dpy-30, histone methyltransferase complex regulatory subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:22571926 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:22571926 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:22110132 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:22571926 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0001776 abnormal circulating sodium level IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:22110132 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:22571926 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:23335223 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0002425 abnormal susceptibility to autoimmune disorder IAGP N RGD:5509061 20200310 MGI PMID:23335223 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20200310 MGI PMID:22110132 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0002776 increased Sertoli cell number IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20200310 MGI PMID:23335223 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0004849 abnormal testis size IAGP N RGD:5509061 20200310 MGI PMID:22110132 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:22571926 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200310 MGI PMID:22110132 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:22110132 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:22571926 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20200310 MGI PMID:23335223 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20200310 MGI PMID:22110132 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20200310 MGI PMID:22110132 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20200310 MGI PMID:22571926 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:23335223 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20200310 MGI PMID:23335223 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0010134 decreased DN3 thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0010135 increased DN4 thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20200310 MGI PMID:22556341 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:22571926 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:22571926 1550809 Tsc22d3 TSC22 domain family, member 3 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:22556341 1550810 Eif4e2 eukaryotic translation initiation factor 4E member 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:22751931 1550810 Eif4e2 eukaryotic translation initiation factor 4E member 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:22751931 1550810 Eif4e2 eukaryotic translation initiation factor 4E member 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20200310 MGI PMID:22751931 1550810 Eif4e2 eukaryotic translation initiation factor 4E member 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20200310 MGI PMID:22751931 1550810 Eif4e2 eukaryotic translation initiation factor 4E member 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22751931 1550812 Or10a4 olfactory receptor family 10 subfamily A member 4 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:15186781 1550812 Or10a4 olfactory receptor family 10 subfamily A member 4 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:8929536 1550812 Or10a4 olfactory receptor family 10 subfamily A member 4 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:21646512 1550812 Or10a4 olfactory receptor family 10 subfamily A member 4 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15157418 1550812 Or10a4 olfactory receptor family 10 subfamily A member 4 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17537788 1550812 Or10a4 olfactory receptor family 10 subfamily A member 4 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23035080 1550812 Or10a4 olfactory receptor family 10 subfamily A member 4 gene MP:0009946 abnormal olfactory bulb layer morphology IAGP N RGD:5509061 20161229 MGI PMID:23884929 1550812 Or10a4 olfactory receptor family 10 subfamily A member 4 gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15186781 1550812 Or10a4 olfactory receptor family 10 subfamily A member 4 gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:9546391 1550812 Or10a4 olfactory receptor family 10 subfamily A member 4 gene MP:0020348 decreased olfactory sensory neuron number IAGP N RGD:5509061 20161229 MGI PMID:23884929 1550814 Npas4 neuronal PAS domain protein 4 gene MP:0000243 myoclonus IAGP N RGD:5509061 20200310 MGI PMID:19001414 1550814 Npas4 neuronal PAS domain protein 4 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200310 MGI PMID:18815592 1550814 Npas4 neuronal PAS domain protein 4 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:18815592 1550814 Npas4 neuronal PAS domain protein 4 gene MP:0002064 seizures IAGP N RGD:5509061 20200310 MGI PMID:18815592 1550814 Npas4 neuronal PAS domain protein 4 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:18815592 1550814 Npas4 neuronal PAS domain protein 4 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19001414 1550814 Npas4 neuronal PAS domain protein 4 gene MP:0002183 gliosis IAGP N RGD:5509061 20200310 MGI PMID:19001414 1550814 Npas4 neuronal PAS domain protein 4 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:19001414 1550814 Npas4 neuronal PAS domain protein 4 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:18815592 1550814 Npas4 neuronal PAS domain protein 4 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:19001414 1550814 Npas4 neuronal PAS domain protein 4 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:18815592 1550814 Npas4 neuronal PAS domain protein 4 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20200310 MGI PMID:19001414 1550814 Npas4 neuronal PAS domain protein 4 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20200310 MGI PMID:19001414 1550814 Npas4 neuronal PAS domain protein 4 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:19001414 1550818 Mlkl mixed lineage kinase domain-like gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 1550818 Mlkl mixed lineage kinase domain-like gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20240125 MGI PMID:35064213 1550818 Mlkl mixed lineage kinase domain-like gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20240125 MGI PMID:35064213 1550818 Mlkl mixed lineage kinase domain-like gene MP:0001194 dermatitis IAGP N RGD:5509061 20220407 MGI PMID:34625556 1550818 Mlkl mixed lineage kinase domain-like gene MP:0001876 decreased inflammatory response IEA N RGD:5509061 20200310 MGI 1550818 Mlkl mixed lineage kinase domain-like gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:23835476 1550818 Mlkl mixed lineage kinase domain-like gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 1550818 Mlkl mixed lineage kinase domain-like gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 1550818 Mlkl mixed lineage kinase domain-like gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 1550818 Mlkl mixed lineage kinase domain-like gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20200310 MGI PMID:23835476 1550818 Mlkl mixed lineage kinase domain-like gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 1550818 Mlkl mixed lineage kinase domain-like gene MP:0006043 decreased apoptosis IEA N RGD:5509061 20200310 MGI 1550818 Mlkl mixed lineage kinase domain-like gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 1550818 Mlkl mixed lineage kinase domain-like gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20200310 MGI PMID:23835476 1550818 Mlkl mixed lineage kinase domain-like gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20200310 MGI PMID:24012422 1550818 Mlkl mixed lineage kinase domain-like gene MP:0012555 decreased cell death IEA N RGD:5509061 20200310 MGI 1550818 Mlkl mixed lineage kinase domain-like gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20200310 MGI PMID:24557836 1550818 Mlkl mixed lineage kinase domain-like gene MP:0013648 increased CD11b-high dendritic cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20141003 MGI 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000373 belly spot IAGP N RGD:5509061 20181122 MGI PMID:28431046 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000433 microcephaly IEA N RGD:5509061 20141003 MGI 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:16192310 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16287714 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:18955569 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:18955569 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:12932351 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11163203 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:16192310 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0001237 enlarged spinous cells IAGP N RGD:5509061 20141003 MGI PMID:16192310 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:16192310 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:16192310 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0001293 anophthalmia IEA N RGD:5509061 20141003 MGI 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:16192310 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12932351 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12932351 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20160512 MGI PMID:17637742 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11163203 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:16192310 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20160512 MGI PMID:17637742 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:16192310 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12932351 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24752179 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002295 abnormal pulmonary circulation IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16287714 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16287714 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002639 micrognathia IEA N RGD:5509061 20141003 MGI 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:16192310 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0002939 head spot IAGP N RGD:5509061 20181122 MGI PMID:28431046 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20160512 MGI PMID:17637742 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20160512 MGI PMID:17637742 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0003800 monodactyly IAGP N RGD:5509061 20141003 MGI PMID:16192310 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:16192310 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:16192310 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20160304 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12932351 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:18955569 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:18955569 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12932351 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18955569 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18955569 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12932351 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18955569 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:11163203 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0008802 abnormal intestinal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0009476 enlarged cecum IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0009483 enlarged ileum IAGP N RGD:5509061 20160304 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20181122 MGI PMID:28431046 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20160512 MGI PMID:17637742 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20160512 MGI PMID:17637742 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010413 complete atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20141003 MGI 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010453 abnormal coronary vein morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010482 abnormal aortic sinus morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010595 abnormal aortic valve cusp morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010602 abnormal pulmonary valve cusp morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010656 thick myocardium IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0010998 pulmonary alveolar proteinosis IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11163203 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16192310 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20181122 MGI PMID:28431046 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11163203 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16287714 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0011648 thick heart valve cusps IAGP N RGD:5509061 20160107 MGI PMID:26100917 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0011684 coronary-cameral fistula to heart right ventricle IEA N RGD:5509061 20141003 MGI 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:21518954 1550820 Smarca4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 gene MP:0013958 decreased small intestine length IAGP N RGD:5509061 20160304 MGI PMID:21518954 1550821 Pkp4 plakophilin 4 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1550821 Pkp4 plakophilin 4 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220519 MGI 1550821 Pkp4 plakophilin 4 gene MP:0001523 impaired righting response IEA N RGD:5509061 20170105 MGI 1550821 Pkp4 plakophilin 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12904583 1550821 Pkp4 plakophilin 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 1550821 Pkp4 plakophilin 4 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220519 MGI 1550821 Pkp4 plakophilin 4 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220519 MGI 1550821 Pkp4 plakophilin 4 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1550821 Pkp4 plakophilin 4 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20211021 MGI 1550822 Prcp prolylcarboxypeptidase (angiotensinase C) gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19620781 1550822 Prcp prolylcarboxypeptidase (angiotensinase C) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19620781 1550822 Prcp prolylcarboxypeptidase (angiotensinase C) gene MP:0001297 microphthalmia IEA N RGD:5509061 20240523 MGI 1550822 Prcp prolylcarboxypeptidase (angiotensinase C) gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 1550822 Prcp prolylcarboxypeptidase (angiotensinase C) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:19620781 1550822 Prcp prolylcarboxypeptidase (angiotensinase C) gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19620781 1550822 Prcp prolylcarboxypeptidase (angiotensinase C) gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:19620781 1550822 Prcp prolylcarboxypeptidase (angiotensinase C) gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19620781 1550822 Prcp prolylcarboxypeptidase (angiotensinase C) gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19620781 1550822 Prcp prolylcarboxypeptidase (angiotensinase C) gene MP:0009291 decreased femoral fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19620781 1550822 Prcp prolylcarboxypeptidase (angiotensinase C) gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19620781 1550822 Prcp prolylcarboxypeptidase (angiotensinase C) gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19620781 1550822 Prcp prolylcarboxypeptidase (angiotensinase C) gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:19620781 1550824 Ly6k lymphocyte antigen 6 family member K gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:24501175 1550824 Ly6k lymphocyte antigen 6 family member K gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20200310 MGI PMID:24501175 1550824 Ly6k lymphocyte antigen 6 family member K gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220303 MGI PMID:24501175 1550831 Mdh1b malate dehydrogenase 1B, NAD (soluble) gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1550833 Dync1li2 dynein, cytoplasmic 1 light intermediate chain 2 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1550833 Dync1li2 dynein, cytoplasmic 1 light intermediate chain 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1550833 Dync1li2 dynein, cytoplasmic 1 light intermediate chain 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1550833 Dync1li2 dynein, cytoplasmic 1 light intermediate chain 2 gene MP:0001925 male infertility IEA N RGD:5509061 20220811 MGI 1550833 Dync1li2 dynein, cytoplasmic 1 light intermediate chain 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1550834 Iars2 isoleucine-tRNA synthetase 2, mitochondrial gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200310 MGI 1550834 Iars2 isoleucine-tRNA synthetase 2, mitochondrial gene MP:0002608 increased hematocrit IEA N RGD:5509061 20201022 MGI 1550834 Iars2 isoleucine-tRNA synthetase 2, mitochondrial gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200310 MGI 1550834 Iars2 isoleucine-tRNA synthetase 2, mitochondrial gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1550834 Iars2 isoleucine-tRNA synthetase 2, mitochondrial gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1550839 Zyx zyxin gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16505170 1550839 Zyx zyxin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12482962 1550839 Zyx zyxin gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:16505170 1550839 Zyx zyxin gene MP:0011707 impaired fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:16505170 1550839 Zyx zyxin gene MP:0011709 increased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:16505170 1550845 Akap6 A kinase anchor protein 6 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:16337591 1550845 Akap6 A kinase anchor protein 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16337591 1550845 Akap6 A kinase anchor protein 6 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141120 MGI PMID:24812305 1550845 Akap6 A kinase anchor protein 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141120 MGI PMID:24812305 1550845 Akap6 A kinase anchor protein 6 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141120 MGI PMID:24812305 1550845 Akap6 A kinase anchor protein 6 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141120 MGI PMID:24812305 1550845 Akap6 A kinase anchor protein 6 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141120 MGI PMID:24812305 1550845 Akap6 A kinase anchor protein 6 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141120 MGI PMID:24812305 1550845 Akap6 A kinase anchor protein 6 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141120 MGI PMID:24812305 1550845 Akap6 A kinase anchor protein 6 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141120 MGI PMID:24812305 1550845 Akap6 A kinase anchor protein 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16337591 1550845 Akap6 A kinase anchor protein 6 gene MP:0011915 increased heart left atrium weight IAGP N RGD:5509061 20141120 MGI PMID:24812305 1550845 Akap6 A kinase anchor protein 6 gene MP:0012688 abnormal heart ventricles weight IAGP N RGD:5509061 20141120 MGI PMID:24812305 1550845 Akap6 A kinase anchor protein 6 gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:24812305 1550846 Rer1 retention in endoplasmic reticulum sorting receptor 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20200310 MGI PMID:21187406 1550846 Rer1 retention in endoplasmic reticulum sorting receptor 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1550846 Rer1 retention in endoplasmic reticulum sorting receptor 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20200310 MGI 1550846 Rer1 retention in endoplasmic reticulum sorting receptor 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1550846 Rer1 retention in endoplasmic reticulum sorting receptor 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20200310 MGI PMID:21187406 1550846 Rer1 retention in endoplasmic reticulum sorting receptor 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1550846 Rer1 retention in endoplasmic reticulum sorting receptor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550846 Rer1 retention in endoplasmic reticulum sorting receptor 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1550846 Rer1 retention in endoplasmic reticulum sorting receptor 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1550848 Klhl20 kelch-like 20 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20200310 MGI PMID:22511632 1550848 Klhl20 kelch-like 20 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:22511632 1550848 Klhl20 kelch-like 20 gene MP:0002161 abnormal fertility/fecundity IEA N RGD:5509061 20111116 MGI 1550848 Klhl20 kelch-like 20 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20200310 MGI PMID:22511632 1550848 Klhl20 kelch-like 20 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20200310 MGI PMID:22511632 1550848 Klhl20 kelch-like 20 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:22511632 1550848 Klhl20 kelch-like 20 gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20200310 MGI PMID:22511632 1550848 Klhl20 kelch-like 20 gene MP:0020857 cornea epithelium hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:22511632 1550849 Ccna2 cyclin A2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19592082 1550849 Ccna2 cyclin A2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19592082 1550849 Ccna2 cyclin A2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19592082 1550849 Ccna2 cyclin A2 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:19592082 1550849 Ccna2 cyclin A2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19592082 1550849 Ccna2 cyclin A2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:10864467 1550849 Ccna2 cyclin A2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:8988174 1550849 Ccna2 cyclin A2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19592082 1550849 Ccna2 cyclin A2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19592082 1550849 Ccna2 cyclin A2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19592082 1550849 Ccna2 cyclin A2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:19592082 1550849 Ccna2 cyclin A2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19592082 1550849 Ccna2 cyclin A2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19592082 1550849 Ccna2 cyclin A2 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19592082 1550849 Ccna2 cyclin A2 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19592082 1550849 Ccna2 cyclin A2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19592082 1550849 Ccna2 cyclin A2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8988174 1550852 Arr3 arrestin 3, retinal gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20220811 MGI 1550852 Arr3 arrestin 3, retinal gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1550852 Arr3 arrestin 3, retinal gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18701071 1550852 Arr3 arrestin 3, retinal gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20240523 MGI 1550853 Gnb3 guanine nucleotide binding protein (G protein), beta 3 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22895717 1550853 Gnb3 guanine nucleotide binding protein (G protein), beta 3 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22895717 1550853 Gnb3 guanine nucleotide binding protein (G protein), beta 3 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22895717 1550853 Gnb3 guanine nucleotide binding protein (G protein), beta 3 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22895717 1550853 Gnb3 guanine nucleotide binding protein (G protein), beta 3 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22895717 1550853 Gnb3 guanine nucleotide binding protein (G protein), beta 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22895717 1550856 Ncam2 neural cell adhesion molecule 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:16531066 1550856 Ncam2 neural cell adhesion molecule 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1550856 Ncam2 neural cell adhesion molecule 2 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:16531066 1550856 Ncam2 neural cell adhesion molecule 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1550856 Ncam2 neural cell adhesion molecule 2 gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20211021 MGI 1550856 Ncam2 neural cell adhesion molecule 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1550856 Ncam2 neural cell adhesion molecule 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1550856 Ncam2 neural cell adhesion molecule 2 gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20211021 MGI 1550856 Ncam2 neural cell adhesion molecule 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1550856 Ncam2 neural cell adhesion molecule 2 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20170314 MGI PMID:25875008 1550857 Cep350 centrosomal protein 350 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1550857 Cep350 centrosomal protein 350 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1550857 Cep350 centrosomal protein 350 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1550861 Plg plasminogen gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9294211 1550861 Plg plasminogen gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16554301 1550861 Plg plasminogen gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:7705657 1550861 Plg plasminogen gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:20653841 1550861 Plg plasminogen gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:9473227 1550861 Plg plasminogen gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:15333838 1550861 Plg plasminogen gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:20653841 1550861 Plg plasminogen gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:7586361 1550861 Plg plasminogen gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:7705657 1550861 Plg plasminogen gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:7705657 1550861 Plg plasminogen gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:7705657 1550861 Plg plasminogen gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:11003846 1550861 Plg plasminogen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:20653841 1550861 Plg plasminogen gene MP:0001139 abnormal vagina morphology IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:7705657 1550861 Plg plasminogen gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:9294211 1550861 Plg plasminogen gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15333838 1550861 Plg plasminogen gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7586361 1550861 Plg plasminogen gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9473227 1550861 Plg plasminogen gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12417566 1550861 Plg plasminogen gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17395831 1550861 Plg plasminogen gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:9671388 1550861 Plg plasminogen gene MP:0001310 abnormal conjunctiva morphology IAGP N RGD:5509061 20141003 MGI PMID:9473227 1550861 Plg plasminogen gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:9473227 1550861 Plg plasminogen gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:17395831 1550861 Plg plasminogen gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:7705657 1550861 Plg plasminogen gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20653841 1550861 Plg plasminogen gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:8612226 1550861 Plg plasminogen gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12417566 1550861 Plg plasminogen gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:9473227 1550861 Plg plasminogen gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:9473227 1550861 Plg plasminogen gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:11003846 1550861 Plg plasminogen gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9671388 1550861 Plg plasminogen gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11003846 1550861 Plg plasminogen gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:7586361 1550861 Plg plasminogen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17395831 1550861 Plg plasminogen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7586361 1550861 Plg plasminogen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9294211 1550861 Plg plasminogen gene MP:0002249 abnormal larynx morphology IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:12417566 1550861 Plg plasminogen gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:7586361 1550861 Plg plasminogen gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:7586361 1550861 Plg plasminogen gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0003273 duodenal ulcer IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0003282 gastric ulcer IAGP N RGD:5509061 20141003 MGI PMID:7586361 1550861 Plg plasminogen gene MP:0003282 gastric ulcer IAGP N RGD:5509061 20141003 MGI PMID:7705657 1550861 Plg plasminogen gene MP:0003282 gastric ulcer IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0003300 gastrointestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0003305 proctitis IAGP N RGD:5509061 20150702 MGI PMID:7705657 1550861 Plg plasminogen gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15333838 1550861 Plg plasminogen gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20653841 1550861 Plg plasminogen gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:7586361 1550861 Plg plasminogen gene MP:0003434 decreased susceptibility to induced choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:12657615 1550861 Plg plasminogen gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:9373263 1550861 Plg plasminogen gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:9275201 1550861 Plg plasminogen gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17301181 1550861 Plg plasminogen gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17395831 1550861 Plg plasminogen gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17395831 1550861 Plg plasminogen gene MP:0004481 abnormal conjunctival epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9473227 1550861 Plg plasminogen gene MP:0004547 esophageal ulcer IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0005035 perianal ulcer IAGP N RGD:5509061 20141003 MGI PMID:7705657 1550861 Plg plasminogen gene MP:0005035 perianal ulcer IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:7705657 1550861 Plg plasminogen gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:9473227 1550861 Plg plasminogen gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:9294211 1550861 Plg plasminogen gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:9473227 1550861 Plg plasminogen gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11557572 1550861 Plg plasminogen gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9473227 1550861 Plg plasminogen gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:7586361 1550861 Plg plasminogen gene MP:0006137 venoocclusion IAGP N RGD:5509061 20141003 MGI PMID:7705657 1550861 Plg plasminogen gene MP:0006164 ectropion IAGP N RGD:5509061 20141003 MGI PMID:9473227 1550861 Plg plasminogen gene MP:0006203 eye hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9473227 1550861 Plg plasminogen gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:11003846 1550861 Plg plasminogen gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:11003846 1550861 Plg plasminogen gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17301181 1550861 Plg plasminogen gene MP:0009507 abnormal mammary gland connective tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11003846 1550861 Plg plasminogen gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15333838 1550861 Plg plasminogen gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9373263 1550861 Plg plasminogen gene MP:0010211 abnormal acute phase protein level IAGP N RGD:5509061 20141003 MGI PMID:12657615 1550861 Plg plasminogen gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:11003846 1550861 Plg plasminogen gene MP:0011507 abnormal kidney thrombosis IAGP N RGD:5509061 20141003 MGI PMID:8929539 1550861 Plg plasminogen gene MP:0012194 decreased keratinocyte migration IAGP N RGD:5509061 20200625 MGI PMID:7705657 1550861 Plg plasminogen gene MP:0012331 increased circulating fibrinogen level IAGP N RGD:5509061 20141003 MGI PMID:20653841 1550861 Plg plasminogen gene MP:0020856 absent cornea epithelium IAGP N RGD:5509061 20181101 MGI PMID:9473227 1550862 Plekhg5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18757825 1550862 Plekhg5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5 gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18757825 1550862 Plekhg5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23253477 1550862 Plekhg5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23253477 1550862 Plekhg5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:23253477 1550862 Plekhg5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:23253477 1550862 Plekhg5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5 gene MP:0003410 abnormal artery development IAGP N RGD:5509061 20141003 MGI PMID:18757825 1550862 Plekhg5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23253477 1550862 Plekhg5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:23253477 1550862 Plekhg5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18757825 1550862 Plekhg5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23253477 1550862 Plekhg5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18757825 1550864 Cd300lb CD300 molecule like family member B gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20200310 MGI PMID:20566714 1550865 Gapdhs glyceraldehyde-3-phosphate dehydrogenase, spermatogenic gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:15546993 1550865 Gapdhs glyceraldehyde-3-phosphate dehydrogenase, spermatogenic gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:15546993 1550867 Kif26a kinesin family member 26A gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:19914172 1550867 Kif26a kinesin family member 26A gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:19914172 1550867 Kif26a kinesin family member 26A gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19914172 1550867 Kif26a kinesin family member 26A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19914172 1550867 Kif26a kinesin family member 26A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19914172 1550867 Kif26a kinesin family member 26A gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:19914172 1550867 Kif26a kinesin family member 26A gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20141003 MGI PMID:19914172 1550867 Kif26a kinesin family member 26A gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:19914172 1550867 Kif26a kinesin family member 26A gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:19914172 1550867 Kif26a kinesin family member 26A gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:19914172 1550867 Kif26a kinesin family member 26A gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19914172 1550867 Kif26a kinesin family member 26A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19914172 1550868 Ptpn7 protein tyrosine phosphatase, non-receptor type 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11564869 1550871 Ift81 intraflagellar transport 81 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1550871 Ift81 intraflagellar transport 81 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1550871 Ift81 intraflagellar transport 81 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1550871 Ift81 intraflagellar transport 81 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1550871 Ift81 intraflagellar transport 81 gene MP:0001925 male infertility IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 1550871 Ift81 intraflagellar transport 81 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1550871 Ift81 intraflagellar transport 81 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1550871 Ift81 intraflagellar transport 81 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1550871 Ift81 intraflagellar transport 81 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550871 Ift81 intraflagellar transport 81 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0014468 disorganized sperm mitochondrial sheath IAGP N RGD:5509061 20240613 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550871 Ift81 intraflagellar transport 81 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20220217 MGI PMID:32233951 1550874 Ncapg2 non-SMC condensin II complex, subunit G2 gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20200310 MGI PMID:14729962 1550874 Ncapg2 non-SMC condensin II complex, subunit G2 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20200310 MGI PMID:14729962 1550874 Ncapg2 non-SMC condensin II complex, subunit G2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:14729962 1550874 Ncapg2 non-SMC condensin II complex, subunit G2 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20200310 MGI PMID:14729962 1550877 Dut deoxyuridine triphosphatase gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20200806 MGI PMID:30987342 1550877 Dut deoxyuridine triphosphatase gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20200806 MGI PMID:30987342 1550877 Dut deoxyuridine triphosphatase gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200806 MGI PMID:30987342 1550880 Smap2 small ArfGAP 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20220922 MGI PMID:26296315 1550880 Smap2 small ArfGAP 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20220922 MGI PMID:23864717 1550880 Smap2 small ArfGAP 2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220922 MGI PMID:23864717 1550880 Smap2 small ArfGAP 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220922 MGI PMID:23864717 1550880 Smap2 small ArfGAP 2 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220922 MGI PMID:23864717 1550880 Smap2 small ArfGAP 2 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20220922 MGI PMID:26296315 1550880 Smap2 small ArfGAP 2 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220922 MGI PMID:23864717 1550880 Smap2 small ArfGAP 2 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20220922 MGI PMID:23864717 1550880 Smap2 small ArfGAP 2 gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20220922 MGI PMID:23864717 1550880 Smap2 small ArfGAP 2 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220922 MGI PMID:23864717 1550880 Smap2 small ArfGAP 2 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220922 MGI PMID:23864717 1550880 Smap2 small ArfGAP 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20220922 MGI PMID:26296315 1550880 Smap2 small ArfGAP 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20220922 MGI PMID:26296315 1550880 Smap2 small ArfGAP 2 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220922 MGI PMID:23864717 1550880 Smap2 small ArfGAP 2 gene MP:0031355 abnormal proacrosomal vesicle fusion IAGP N RGD:5509061 20220922 MGI PMID:23864717 1550880 Smap2 small ArfGAP 2 gene MP:0031389 abnormal ectoplasmic specialization morphology IAGP N RGD:5509061 20220922 MGI PMID:23864717 1550881 Pabpn1 poly(A) binding protein, nuclear 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20180201 MGI PMID:28575395 1550881 Pabpn1 poly(A) binding protein, nuclear 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20180201 MGI PMID:28575395 1550881 Pabpn1 poly(A) binding protein, nuclear 1 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20180201 MGI PMID:28575395 1550881 Pabpn1 poly(A) binding protein, nuclear 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180201 MGI PMID:28575395 1550881 Pabpn1 poly(A) binding protein, nuclear 1 gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20180201 MGI PMID:28575395 1550881 Pabpn1 poly(A) binding protein, nuclear 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20180201 MGI PMID:28575395 1550881 Pabpn1 poly(A) binding protein, nuclear 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20180201 MGI PMID:28575395 1550881 Pabpn1 poly(A) binding protein, nuclear 1 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20180201 MGI PMID:28575395 1550881 Pabpn1 poly(A) binding protein, nuclear 1 gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20180201 MGI PMID:28575395 1550881 Pabpn1 poly(A) binding protein, nuclear 1 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20180201 MGI PMID:28575395 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0000373 belly spot IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0000706 small thymus IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20241010 MGI 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20241010 MGI 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0002418 increased susceptibility to viral infection IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0002582 disorganized extraembryonic tissue IEA N RGD:5509061 20241010 MGI 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0002938 white spotting IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20241010 MGI 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241010 MGI 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0009791 increased susceptibility to viral infection induced morbidity/mortality IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0010130 decreased DN1 thymic pro-T cell number IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550882 Snrnp40 small nuclear ribonucleoprotein 40 (U5) gene MP:0013893 decreased common lymphocyte progenitor cell number IAGP N RGD:5509061 20210520 MGI PMID:31427773 1550883 Hrc histidine rich calcium binding protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17030629 1550883 Hrc histidine rich calcium binding protein gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17030629 1550883 Hrc histidine rich calcium binding protein gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20171026 MGI PMID:28859293 1550883 Hrc histidine rich calcium binding protein gene MP:0002083 premature death IAGP N RGD:5509061 20171026 MGI PMID:28859293 1550883 Hrc histidine rich calcium binding protein gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20171026 MGI PMID:28859293 1550883 Hrc histidine rich calcium binding protein gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20171026 MGI PMID:28859293 1550883 Hrc histidine rich calcium binding protein gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:17030629 1550883 Hrc histidine rich calcium binding protein gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20171026 MGI PMID:28859293 1550883 Hrc histidine rich calcium binding protein gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:17030629 1550883 Hrc histidine rich calcium binding protein gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20171026 MGI PMID:28859293 1550883 Hrc histidine rich calcium binding protein gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17030629 1550883 Hrc histidine rich calcium binding protein gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20171026 MGI PMID:28859293 1550883 Hrc histidine rich calcium binding protein gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20171026 MGI PMID:28859293 1550883 Hrc histidine rich calcium binding protein gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20171026 MGI PMID:28859293 1550883 Hrc histidine rich calcium binding protein gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20171026 MGI PMID:28859293 1550883 Hrc histidine rich calcium binding protein gene MP:0020345 abnormal myocardial fiber currents IAGP N RGD:5509061 20171026 MGI PMID:28859293 1550883 Hrc histidine rich calcium binding protein gene MP:0020419 decreased cardiac muscle relaxation IAGP N RGD:5509061 20171026 MGI PMID:28859293 1550884 Prepl prolyl endopeptidase-like gene MP:0000746 weakness IAGP N RGD:5509061 20200310 MGI PMID:24586561 1550884 Prepl prolyl endopeptidase-like gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:24586561 1550884 Prepl prolyl endopeptidase-like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:24586561 1550884 Prepl prolyl endopeptidase-like gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:24586561 1550884 Prepl prolyl endopeptidase-like gene MP:0001333 absent optic nerve IEA N RGD:5509061 20200514 MGI 1550884 Prepl prolyl endopeptidase-like gene MP:0001406 abnormal gait IEA N RGD:5509061 20200514 MGI 1550884 Prepl prolyl endopeptidase-like gene MP:0001523 impaired righting response IAGP N RGD:5509061 20200310 MGI PMID:24586561 1550884 Prepl prolyl endopeptidase-like gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:24586561 1550884 Prepl prolyl endopeptidase-like gene MP:0004144 hypotonia IAGP N RGD:5509061 20200310 MGI PMID:24586561 1550884 Prepl prolyl endopeptidase-like gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200310 MGI PMID:24586561 1550884 Prepl prolyl endopeptidase-like gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:15964823 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:21840293 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22952456 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:16983341 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:16983341 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16983341 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:16983341 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:16983341 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:16983341 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:22952456 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:15964823 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:22952456 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:15964823 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:17174946 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15964823 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:22952456 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:22952456 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:15964823 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:15964823 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:16983341 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:22952456 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:16983341 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:21840293 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16983341 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0004265 abnormal placental transport IAGP N RGD:5509061 20141003 MGI PMID:15964823 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17174946 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0004560 abnormal chorionic plate morphology IAGP N RGD:5509061 20141003 MGI PMID:15964823 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:21840293 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16983341 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17174946 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15964823 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:21840293 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:21840293 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17174946 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21840293 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21840293 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0009477 small cecum IAGP N RGD:5509061 20141003 MGI PMID:21840293 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:16983341 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21840293 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:21840293 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:21840293 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16983341 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15964823 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16983341 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17174946 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:15964823 1550885 Spint1 serine protease inhibitor, Kunitz type 1 gene MP:0030605 abnormal corneocyte morphology IAGP N RGD:5509061 20180628 MGI PMID:16983341 1550887 Mgp matrix Gla protein gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20200310 MGI PMID:12391016 1550887 Mgp matrix Gla protein gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:21765215 1550887 Mgp matrix Gla protein gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:21765215 1550887 Mgp matrix Gla protein gene MP:0001255 decreased body height IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:23994172 1550887 Mgp matrix Gla protein gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:12391016 1550887 Mgp matrix Gla protein gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:12391016 1550887 Mgp matrix Gla protein gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20200310 MGI PMID:23994172 1550887 Mgp matrix Gla protein gene MP:0002626 increased heart rate IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0002989 small kidney IAGP N RGD:5509061 20200310 MGI PMID:21765215 1550887 Mgp matrix Gla protein gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20200310 MGI PMID:23994172 1550887 Mgp matrix Gla protein gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0003279 aneurysm IAGP N RGD:5509061 20200310 MGI PMID:12391016 1550887 Mgp matrix Gla protein gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0003641 small lung IAGP N RGD:5509061 20200310 MGI PMID:21765215 1550887 Mgp matrix Gla protein gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20200310 MGI PMID:21765215 1550887 Mgp matrix Gla protein gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:21765215 1550887 Mgp matrix Gla protein gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20200310 MGI PMID:23994172 1550887 Mgp matrix Gla protein gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20200310 MGI PMID:23994172 1550887 Mgp matrix Gla protein gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200310 MGI PMID:21765215 1550887 Mgp matrix Gla protein gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20200310 MGI PMID:21765215 1550887 Mgp matrix Gla protein gene MP:0006116 calcified aortic valve IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0006133 calcified artery IAGP N RGD:5509061 20200310 MGI PMID:12391016 1550887 Mgp matrix Gla protein gene MP:0006133 calcified artery IAGP N RGD:5509061 20200310 MGI PMID:23994172 1550887 Mgp matrix Gla protein gene MP:0006133 calcified artery IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20200310 MGI PMID:23994172 1550887 Mgp matrix Gla protein gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200310 MGI PMID:23994172 1550887 Mgp matrix Gla protein gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20200310 MGI PMID:23994172 1550887 Mgp matrix Gla protein gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0010480 pulmonary arteriovenous malformation IAGP N RGD:5509061 20200310 MGI PMID:21765215 1550887 Mgp matrix Gla protein gene MP:0010522 calcified aorta IAGP N RGD:5509061 20201112 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:23994172 1550887 Mgp matrix Gla protein gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20200310 MGI PMID:23994172 1550887 Mgp matrix Gla protein gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20200310 MGI PMID:23994172 1550887 Mgp matrix Gla protein gene MP:0010962 decreased compact bone mass IAGP N RGD:5509061 20200310 MGI PMID:23994172 1550887 Mgp matrix Gla protein gene MP:0010988 abnormal bronchial cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:9052783 1550887 Mgp matrix Gla protein gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20200310 MGI PMID:21765215 1550887 Mgp matrix Gla protein gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20200310 MGI PMID:23994172 1550887 Mgp matrix Gla protein gene MP:0030984 increased circulating osteocalcin level IAGP N RGD:5509061 20200310 MGI PMID:23994172 1550889 Plpp2 phospholipid phosphatase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10992322 1550897 Wdr44 WD repeat domain 44 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:24252660 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:24252660 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:24252660 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:24252660 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230119 MGI 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20200310 MGI PMID:24252660 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200310 MGI PMID:24252660 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20200310 MGI PMID:24252660 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20200310 MGI PMID:24252660 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20200310 MGI PMID:24252660 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20200310 MGI PMID:24252660 1550898 Chd5 chromodomain helicase DNA binding protein 5 gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20230119 MGI 1550902 Arhgap8 Rho GTPase activating protein 8 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1550902 Arhgap8 Rho GTPase activating protein 8 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1550903 Slc12a7 solute carrier family 12, member 7 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11976689 1550903 Slc12a7 solute carrier family 12, member 7 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:11976689 1550903 Slc12a7 solute carrier family 12, member 7 gene MP:0000044 absent organ of Corti IAGP N RGD:5509061 20141003 MGI PMID:11976689 1550903 Slc12a7 solute carrier family 12, member 7 gene MP:0000525 renal tubular acidosis IAGP N RGD:5509061 20141003 MGI PMID:11976689 1550903 Slc12a7 solute carrier family 12, member 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11976689 1550903 Slc12a7 solute carrier family 12, member 7 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11976689 1550903 Slc12a7 solute carrier family 12, member 7 gene MP:0001967 deafness IAGP N RGD:5509061 20160929 MGI PMID:27534441 1550903 Slc12a7 solute carrier family 12, member 7 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:11976689 1550903 Slc12a7 solute carrier family 12, member 7 gene MP:0004403 absent cochlear outer hair cells IAGP N RGD:5509061 20141003 MGI PMID:11976689 1550903 Slc12a7 solute carrier family 12, member 7 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11976689 1550903 Slc12a7 solute carrier family 12, member 7 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:11976689 1550903 Slc12a7 solute carrier family 12, member 7 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:11976689 1550903 Slc12a7 solute carrier family 12, member 7 gene MP:0009349 increased urine pH IAGP N RGD:5509061 20141003 MGI PMID:11976689 1550903 Slc12a7 solute carrier family 12, member 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1550903 Slc12a7 solute carrier family 12, member 7 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11976689 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0003865 lymph node inflammation IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0006173 abnormal myeloid dendritic cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0006412 abnormal T cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550908 Tnfaip8l2 tumor necrosis factor, alpha-induced protein 8-like 2 gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20200310 MGI PMID:18455983 1550912 St7 suppression of tumorigenicity 7 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1550912 St7 suppression of tumorigenicity 7 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1550912 St7 suppression of tumorigenicity 7 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1550912 St7 suppression of tumorigenicity 7 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1550912 St7 suppression of tumorigenicity 7 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1550915 Mrgpre MAS-related GPR, member E gene MP:0003177 allodynia IAGP N RGD:5509061 20150924 MGI PMID:18197975 1550915 Mrgpre MAS-related GPR, member E gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20211021 MGI 1550917 Nsmce1 NSE1 homolog, SMC5-SMC6 complex component gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200514 MGI 1550917 Nsmce1 NSE1 homolog, SMC5-SMC6 complex component gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200514 MGI 1550917 Nsmce1 NSE1 homolog, SMC5-SMC6 complex component gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20200514 MGI 1550917 Nsmce1 NSE1 homolog, SMC5-SMC6 complex component gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210128 MGI 1550917 Nsmce1 NSE1 homolog, SMC5-SMC6 complex component gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210128 MGI 1550917 Nsmce1 NSE1 homolog, SMC5-SMC6 complex component gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1550917 Nsmce1 NSE1 homolog, SMC5-SMC6 complex component gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 1550917 Nsmce1 NSE1 homolog, SMC5-SMC6 complex component gene MP:0009709 hydrometra IEA N RGD:5509061 20200514 MGI 1550917 Nsmce1 NSE1 homolog, SMC5-SMC6 complex component gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1550917 Nsmce1 NSE1 homolog, SMC5-SMC6 complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550917 Nsmce1 NSE1 homolog, SMC5-SMC6 complex component gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1550927 Git2 GIT ArfGAP 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16715100 1550927 Git2 GIT ArfGAP 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16715100 1550927 Git2 GIT ArfGAP 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:16715100 1550927 Git2 GIT ArfGAP 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:23870131 1550927 Git2 GIT ArfGAP 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17565117 1550927 Git2 GIT ArfGAP 2 gene MP:0002333 abnormal lung compliance IAGP N RGD:5509061 20141003 MGI PMID:16715100 1550927 Git2 GIT ArfGAP 2 gene MP:0002415 abnormal neutrophil differentiation IAGP N RGD:5509061 20141003 MGI PMID:16715100 1550927 Git2 GIT ArfGAP 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16715100 1550927 Git2 GIT ArfGAP 2 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:20431621 1550927 Git2 GIT ArfGAP 2 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20431621 1550927 Git2 GIT ArfGAP 2 gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:20431621 1550927 Git2 GIT ArfGAP 2 gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:16715100 1550927 Git2 GIT ArfGAP 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20431621 1550927 Git2 GIT ArfGAP 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20431621 1550927 Git2 GIT ArfGAP 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20431621 1550927 Git2 GIT ArfGAP 2 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:20431621 1550927 Git2 GIT ArfGAP 2 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:16715100 1550929 Phldb1 pleckstrin homology like domain, family B, member 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20201022 MGI 1550929 Phldb1 pleckstrin homology like domain, family B, member 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1550929 Phldb1 pleckstrin homology like domain, family B, member 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1550929 Phldb1 pleckstrin homology like domain, family B, member 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20231207 MGI 1550929 Phldb1 pleckstrin homology like domain, family B, member 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1550929 Phldb1 pleckstrin homology like domain, family B, member 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200402 MGI 1550931 Mapk15 mitogen-activated protein kinase 15 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1550931 Mapk15 mitogen-activated protein kinase 15 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20201022 MGI 1550931 Mapk15 mitogen-activated protein kinase 15 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1550931 Mapk15 mitogen-activated protein kinase 15 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1550931 Mapk15 mitogen-activated protein kinase 15 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20231207 MGI 1550933 Laptm4a lysosomal-associated protein transmembrane 4A gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1550933 Laptm4a lysosomal-associated protein transmembrane 4A gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1550933 Laptm4a lysosomal-associated protein transmembrane 4A gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20160421 MGI 1550933 Laptm4a lysosomal-associated protein transmembrane 4A gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20160421 MGI 1550933 Laptm4a lysosomal-associated protein transmembrane 4A gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1550934 Enc1 ectodermal-neural cortex 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20170105 MGI 1550934 Enc1 ectodermal-neural cortex 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1550934 Enc1 ectodermal-neural cortex 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20170105 MGI 1550934 Enc1 ectodermal-neural cortex 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1550934 Enc1 ectodermal-neural cortex 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170105 MGI 1550934 Enc1 ectodermal-neural cortex 1 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20170105 MGI 1550935 Wdr45 WD repeat domain 45 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1550935 Wdr45 WD repeat domain 45 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0000745 tremors IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0000921 demyelination IAGP N RGD:5509061 20200130 MGI PMID:26000824 1550935 Wdr45 WD repeat domain 45 gene MP:0001260 increased body weight IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220428 MGI 1550935 Wdr45 WD repeat domain 45 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200130 MGI PMID:26000824 1550935 Wdr45 WD repeat domain 45 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20240523 MGI 1550935 Wdr45 WD repeat domain 45 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20200130 MGI PMID:26000824 1550935 Wdr45 WD repeat domain 45 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20210128 MGI 1550935 Wdr45 WD repeat domain 45 gene MP:0001513 limb grasping IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1550935 Wdr45 WD repeat domain 45 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0002833 increased heart weight IEA N RGD:5509061 20240523 MGI 1550935 Wdr45 WD repeat domain 45 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20200130 MGI PMID:26000824 1550935 Wdr45 WD repeat domain 45 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1550935 Wdr45 WD repeat domain 45 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200130 MGI PMID:26000824 1550935 Wdr45 WD repeat domain 45 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1550935 Wdr45 WD repeat domain 45 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1550935 Wdr45 WD repeat domain 45 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0005376 homeostasis/metabolism phenotype IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0005397 hematopoietic system phenotype IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20200130 MGI PMID:26000824 1550935 Wdr45 WD repeat domain 45 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20200130 MGI PMID:26000824 1550935 Wdr45 WD repeat domain 45 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20200130 MGI PMID:26000824 1550935 Wdr45 WD repeat domain 45 gene MP:0008805 decreased circulating amylase level IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20200130 MGI PMID:26000824 1550935 Wdr45 WD repeat domain 45 gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20200130 MGI PMID:26000824 1550935 Wdr45 WD repeat domain 45 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1550935 Wdr45 WD repeat domain 45 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0011897 decreased circulating unsaturated transferrin level IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200130 MGI PMID:26000824 1550935 Wdr45 WD repeat domain 45 gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0020396 abnormal social recognition IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200130 MGI PMID:26000824 1550935 Wdr45 WD repeat domain 45 gene MP:0031213 increased eye anterior chamber depth IAGP N RGD:5509061 20210729 MGI PMID:34043061 1550935 Wdr45 WD repeat domain 45 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:34043061 1550938 Tob2 transducer of ERBB2, 2 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:18358842 1550938 Tob2 transducer of ERBB2, 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18358842 1550938 Tob2 transducer of ERBB2, 2 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:18358842 1550938 Tob2 transducer of ERBB2, 2 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:18358842 1550938 Tob2 transducer of ERBB2, 2 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:18358842 1550938 Tob2 transducer of ERBB2, 2 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:18358842 1550938 Tob2 transducer of ERBB2, 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:18358842 1550939 Ticam2 TIR domain containing adaptor molecule 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:14556004 1550939 Ticam2 TIR domain containing adaptor molecule 2 gene MP:0008555 abnormal interferon secretion IEA N RGD:5509061 20111116 MGI 1550939 Ticam2 TIR domain containing adaptor molecule 2 gene MP:0008561 decreased tumor necrosis factor secretion IEA N RGD:5509061 20111116 MGI 1550939 Ticam2 TIR domain containing adaptor molecule 2 gene MP:0008658 decreased interleukin-1 beta secretion IEA N RGD:5509061 20180215 MGI 1550939 Ticam2 TIR domain containing adaptor molecule 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:14556004 1550939 Ticam2 TIR domain containing adaptor molecule 2 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:28592648 1550941 Nsmaf neutral sphingomyelinase (N-SMase) activation associated factor gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10228161 1550941 Nsmaf neutral sphingomyelinase (N-SMase) activation associated factor gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:10228161 1550941 Nsmaf neutral sphingomyelinase (N-SMase) activation associated factor gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:14985352 1550942 Yod1 YOD1 deubiquitinase gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20221103 MGI 1550942 Yod1 YOD1 deubiquitinase gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20241114 MGI PMID:38789414 1550942 Yod1 YOD1 deubiquitinase gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20241114 MGI PMID:38789414 1550942 Yod1 YOD1 deubiquitinase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20241114 MGI PMID:38789414 1550942 Yod1 YOD1 deubiquitinase gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20241114 MGI PMID:38789414 1550942 Yod1 YOD1 deubiquitinase gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20221103 MGI 1550942 Yod1 YOD1 deubiquitinase gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20241114 MGI PMID:38789414 1550942 Yod1 YOD1 deubiquitinase gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20221103 MGI 1550942 Yod1 YOD1 deubiquitinase gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20221103 MGI 1550942 Yod1 YOD1 deubiquitinase gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20241114 MGI PMID:38789414 1550942 Yod1 YOD1 deubiquitinase gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20241114 MGI PMID:38789414 1550942 Yod1 YOD1 deubiquitinase gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20241114 MGI PMID:38789414 1550942 Yod1 YOD1 deubiquitinase gene MP:0011078 increased macrophage cytokine production IAGP N RGD:5509061 20241114 MGI PMID:38789414 1550942 Yod1 YOD1 deubiquitinase gene MP:0012330 decreased circulating fibrinogen level IAGP N RGD:5509061 20241114 MGI PMID:38789414 1550942 Yod1 YOD1 deubiquitinase gene MP:0012359 increased partial thromboplastin time IAGP N RGD:5509061 20241114 MGI PMID:38789414 1550942 Yod1 YOD1 deubiquitinase gene MP:0031083 increased circulating D-dimer level IAGP N RGD:5509061 20241114 MGI PMID:38789414 1550942 Yod1 YOD1 deubiquitinase gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20241114 MGI PMID:38789414 1550945 Phlpp1 PH domain and leucine rich repeat protein phosphatase 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1550945 Phlpp1 PH domain and leucine rich repeat protein phosphatase 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210520 MGI 1550945 Phlpp1 PH domain and leucine rich repeat protein phosphatase 1 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20200310 MGI PMID:26187040 1550945 Phlpp1 PH domain and leucine rich repeat protein phosphatase 1 gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20200310 MGI PMID:26187040 1550945 Phlpp1 PH domain and leucine rich repeat protein phosphatase 1 gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20200310 MGI PMID:20080691 1550945 Phlpp1 PH domain and leucine rich repeat protein phosphatase 1 gene MP:0020475 delayed circadian behavior phase IAGP N RGD:5509061 20200310 MGI PMID:20080691 1550946 Alkbh3 alkB homolog 3, alpha-ketoglutarate-dependent dioxygenase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16642038 1550946 Alkbh3 alkB homolog 3, alpha-ketoglutarate-dependent dioxygenase gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:16642038 1550948 Uhmk1 U2AF homology motif (UHM) kinase 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:19033656 1550948 Uhmk1 U2AF homology motif (UHM) kinase 1 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20200310 MGI PMID:19033656 1550948 Uhmk1 U2AF homology motif (UHM) kinase 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20200310 MGI PMID:19033656 1550948 Uhmk1 U2AF homology motif (UHM) kinase 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:19033656 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0001488 increased startle reflex IEA N RGD:5509061 20231207 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0001574 abnormal oxygen level IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0002626 increased heart rate IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0003028 alkalosis IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0003032 hypocapnia IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0005585 increased tidal volume IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20220519 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0011939 increased food intake IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20200310 MGI PMID:20399150 1550949 Hif1an hypoxia-inducible factor 1, alpha subunit inhibitor gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:20399150 1550950 Rhbdl1 rhomboid like 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1550950 Rhbdl1 rhomboid like 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1550950 Rhbdl1 rhomboid like 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1550950 Rhbdl1 rhomboid like 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1550950 Rhbdl1 rhomboid like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1550950 Rhbdl1 rhomboid like 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1550951 Rnf141 ring finger protein 141 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23196134 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20200310 MGI PMID:18064678 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:24115439 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:24115439 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:18064678 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:18064678 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:22593209 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20200310 MGI PMID:24115439 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200310 MGI PMID:24115439 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20200310 MGI PMID:18064678 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0004559 small allantois IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20200310 MGI PMID:18064678 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:24115439 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20200310 MGI PMID:24115439 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20200310 MGI PMID:24115439 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0008817 hematoma IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0009845 abnormal neural crest cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20200310 MGI PMID:24115439 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20200310 MGI PMID:24115439 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18064678 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:24115439 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0012675 enlarged floor plate IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0021086 decreased DNA replication IAGP N RGD:5509061 20220310 MGI PMID:24115439 1550955 Rtel1 regulator of telomere elongation helicase 1 gene MP:0030539 abnormal head paraxial mesoderm morphology IAGP N RGD:5509061 20200310 MGI PMID:15210109 1550957 Oxgr1 oxoglutarate (alpha-ketoglutarate) receptor 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20200310 MGI PMID:23504326 1550957 Oxgr1 oxoglutarate (alpha-ketoglutarate) receptor 1 gene MP:0003016 increased circulating bicarbonate level IAGP N RGD:5509061 20200310 MGI PMID:23934124 1550957 Oxgr1 oxoglutarate (alpha-ketoglutarate) receptor 1 gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20200310 MGI PMID:23934124 1550957 Oxgr1 oxoglutarate (alpha-ketoglutarate) receptor 1 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20200310 MGI PMID:23934124 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:25835743 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:7139332 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:9182797 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20200310 MGI PMID:7139332 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0000921 demyelination IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20200310 MGI PMID:9182797 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20200310 MGI PMID:7139332 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0001671 abnormal vitamin absorption IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0002064 seizures IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:14517553 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:9182797 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0002715 decreased glycogen catabolism rate IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:14517553 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:9182797 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0002883 chromatolysis IAGP N RGD:5509061 20200310 MGI PMID:9182797 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:7139332 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:9182797 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0010769 abnormal survival IAGP N RGD:5509061 20200310 MGI PMID:25835743 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0011231 abnormal vitamin E level IAGP N RGD:5509061 20200310 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:7139332 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20200917 MGI PMID:12788952 1550960 Pitpna phosphatidylinositol transfer protein, alpha gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:12788952 1550963 Kcnq5 potassium voltage-gated channel, subfamily Q, member 5 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20141003 MGI PMID:20534576 1550963 Kcnq5 potassium voltage-gated channel, subfamily Q, member 5 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20534576 1550965 Wdr47 WD repeat domain 47 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20200310 MGI 1550965 Wdr47 WD repeat domain 47 gene MP:0001262 decreased body weight IEA N RGD:5509061 20200310 MGI 1550965 Wdr47 WD repeat domain 47 gene MP:0001399 hyperactivity IEA N RGD:5509061 20200310 MGI 1550965 Wdr47 WD repeat domain 47 gene MP:0001513 limb grasping IEA N RGD:5509061 20200310 MGI 1550965 Wdr47 WD repeat domain 47 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20200310 MGI 1550965 Wdr47 WD repeat domain 47 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200310 MGI 1550965 Wdr47 WD repeat domain 47 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20200310 MGI 1550965 Wdr47 WD repeat domain 47 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20200310 MGI 1550965 Wdr47 WD repeat domain 47 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200310 MGI 1550966 Nova1 NOVA alternative splicing regulator 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10719891 1550966 Nova1 NOVA alternative splicing regulator 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:10719891 1550966 Nova1 NOVA alternative splicing regulator 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:10719891 1550966 Nova1 NOVA alternative splicing regulator 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:10719891 1550966 Nova1 NOVA alternative splicing regulator 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10719891 1550966 Nova1 NOVA alternative splicing regulator 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:10719891 1550966 Nova1 NOVA alternative splicing regulator 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10719891 1550967 Hsd17b8 hydroxysteroid 17-beta dehydrogenase 8 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1550969 Sac3d1 SAC3 domain containing 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:18838617 1550969 Sac3d1 SAC3 domain containing 1 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:18838617 1550969 Sac3d1 SAC3 domain containing 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20200310 MGI PMID:18838617 1550969 Sac3d1 SAC3 domain containing 1 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20200310 MGI PMID:18838617 1550969 Sac3d1 SAC3 domain containing 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20200310 MGI PMID:18838617 1550969 Sac3d1 SAC3 domain containing 1 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20200310 MGI PMID:18838617 1550969 Sac3d1 SAC3 domain containing 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:18838617 1550969 Sac3d1 SAC3 domain containing 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18838617 1550974 Ehbp1 EH domain binding protein 1 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20210520 MGI 1550974 Ehbp1 EH domain binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1550974 Ehbp1 EH domain binding protein 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1550975 Gsdme gasdermin E gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16023581 1550975 Gsdme gasdermin E gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16023581 1550975 Gsdme gasdermin E gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180920 MGI PMID:28459430 1550975 Gsdme gasdermin E gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20231207 MGI 1550975 Gsdme gasdermin E gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1550975 Gsdme gasdermin E gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16804542 1550978 Tnfaip1 tumor necrosis factor, alpha-induced protein 1 (endothelial) gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 1550978 Tnfaip1 tumor necrosis factor, alpha-induced protein 1 (endothelial) gene MP:0001391 abnormal tail movements IEA N RGD:5509061 20160804 MGI 1550978 Tnfaip1 tumor necrosis factor, alpha-induced protein 1 (endothelial) gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1550978 Tnfaip1 tumor necrosis factor, alpha-induced protein 1 (endothelial) gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1550978 Tnfaip1 tumor necrosis factor, alpha-induced protein 1 (endothelial) gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20160804 MGI 1550978 Tnfaip1 tumor necrosis factor, alpha-induced protein 1 (endothelial) gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20160804 MGI 1550978 Tnfaip1 tumor necrosis factor, alpha-induced protein 1 (endothelial) gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160804 MGI 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:17438139 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0003606 kidney failure IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0003624 anuria IAGP N RGD:5509061 20200310 MGI PMID:25108225 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20200310 MGI PMID:25108225 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20200310 MGI PMID:25108225 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20200310 MGI PMID:25108225 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0008137 absent podocytes IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20200310 MGI PMID:25108225 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25108225 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17438139 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0011402 renal cast IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0011455 absent glomerular endothelium fenestra IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0011498 abnormal glomerular capsule parietal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0011856 abnormal glomerular filtration barrier function IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0011868 podocyte microvillus transformation IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550979 Magi2 membrane associated guanylate kinase, WW and PDZ domain containing 2 gene MP:0011871 podocyte hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:25271328 1550980 Rbm3 RNA binding motif (RNP1, RRM) protein 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1550980 Rbm3 RNA binding motif (RNP1, RRM) protein 3 gene MP:0002084 abnormal developmental patterning IEA N RGD:5509061 20111116 MGI 1550980 Rbm3 RNA binding motif (RNP1, RRM) protein 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:21684257 1550980 Rbm3 RNA binding motif (RNP1, RRM) protein 3 gene MP:0006386 absent somites IEA N RGD:5509061 20111116 MGI 1550980 Rbm3 RNA binding motif (RNP1, RRM) protein 3 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:21684257 1550981 Omg oligodendrocyte myelin glycoprotein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19672953 1550981 Omg oligodendrocyte myelin glycoprotein gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:18692574 1550982 Zfp111 zinc finger protein 111 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1550982 Zfp111 zinc finger protein 111 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1550982 Zfp111 zinc finger protein 111 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1550984 Mrgprb4 MAS-related GPR, member B4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17618277 1550985 Pank4 pantothenate kinase 4 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20231207 MGI 1550985 Pank4 pantothenate kinase 4 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20210318 MGI PMID:30585370 1550985 Pank4 pantothenate kinase 4 gene MP:0001304 cataract IAGP N RGD:5509061 20210318 MGI PMID:30585370 1550985 Pank4 pantothenate kinase 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1550985 Pank4 pantothenate kinase 4 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20210318 MGI PMID:30585370 1550985 Pank4 pantothenate kinase 4 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20210318 MGI PMID:30585370 1550985 Pank4 pantothenate kinase 4 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20231207 MGI 1550985 Pank4 pantothenate kinase 4 gene MP:0008794 increased lens epithelium apoptosis IAGP N RGD:5509061 20210318 MGI PMID:30585370 1550985 Pank4 pantothenate kinase 4 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 1550992 Usp5 ubiquitin specific peptidase 5 (isopeptidase T) gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20160114 MGI 1550992 Usp5 ubiquitin specific peptidase 5 (isopeptidase T) gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20111116 MGI 1550992 Usp5 ubiquitin specific peptidase 5 (isopeptidase T) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1550993 Bcl7c B cell CLL/lymphoma 7C gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1550993 Bcl7c B cell CLL/lymphoma 7C gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1550994 Mpzl1 myelin protein zero-like 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1550994 Mpzl1 myelin protein zero-like 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20210311 MGI PMID:32584792 1550994 Mpzl1 myelin protein zero-like 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20221215 MGI 1550994 Mpzl1 myelin protein zero-like 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1551003 Tlr2 toll-like receptor 2 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19841034 1551003 Tlr2 toll-like receptor 2 gene MP:0000181 abnormal circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19841034 1551003 Tlr2 toll-like receptor 2 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19841034 1551003 Tlr2 toll-like receptor 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:14656915 1551003 Tlr2 toll-like receptor 2 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:14656915 1551003 Tlr2 toll-like receptor 2 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:16980352 1551003 Tlr2 toll-like receptor 2 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17408640 1551003 Tlr2 toll-like receptor 2 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20885960 1551003 Tlr2 toll-like receptor 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16118350 1551003 Tlr2 toll-like receptor 2 gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:20534434 1551003 Tlr2 toll-like receptor 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16211093 1551003 Tlr2 toll-like receptor 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18250194 1551003 Tlr2 toll-like receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20171214 MGI PMID:28769782 1551003 Tlr2 toll-like receptor 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17408640 1551003 Tlr2 toll-like receptor 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20885960 1551003 Tlr2 toll-like receptor 2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:17403033 1551003 Tlr2 toll-like receptor 2 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:17998311 1551003 Tlr2 toll-like receptor 2 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19841034 1551003 Tlr2 toll-like receptor 2 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19841034 1551003 Tlr2 toll-like receptor 2 gene MP:0001652 colonic necrosis IAGP N RGD:5509061 20141003 MGI PMID:20885960 1551003 Tlr2 toll-like receptor 2 gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17475877 1551003 Tlr2 toll-like receptor 2 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20885960 1551003 Tlr2 toll-like receptor 2 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20885960 1551003 Tlr2 toll-like receptor 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17707128 1551003 Tlr2 toll-like receptor 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19841034 1551003 Tlr2 toll-like receptor 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20407745 1551003 Tlr2 toll-like receptor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17408640 1551003 Tlr2 toll-like receptor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20885960 1551003 Tlr2 toll-like receptor 2 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:15843573 1551003 Tlr2 toll-like receptor 2 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:17626835 1551003 Tlr2 toll-like receptor 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1551003 Tlr2 toll-like receptor 2 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17704767 1551003 Tlr2 toll-like receptor 2 gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:16244651 1551003 Tlr2 toll-like receptor 2 gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:20407745 1551003 Tlr2 toll-like receptor 2 gene MP:0002319 hyperoxia IAGP N RGD:5509061 20141003 MGI PMID:16244651 1551003 Tlr2 toll-like receptor 2 gene MP:0002334 abnormal airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:17626835 1551003 Tlr2 toll-like receptor 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16461338 1551003 Tlr2 toll-like receptor 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11751980 1551003 Tlr2 toll-like receptor 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12091878 1551003 Tlr2 toll-like receptor 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15690042 1551003 Tlr2 toll-like receptor 2 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:11751980 1551003 Tlr2 toll-like receptor 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10549626 1551003 Tlr2 toll-like receptor 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11431423 1551003 Tlr2 toll-like receptor 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11751980 1551003 Tlr2 toll-like receptor 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12091878 1551003 Tlr2 toll-like receptor 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15690042 1551003 Tlr2 toll-like receptor 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16204620 1551003 Tlr2 toll-like receptor 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17118979 1551003 Tlr2 toll-like receptor 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17353199 1551003 Tlr2 toll-like receptor 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17998311 1551003 Tlr2 toll-like receptor 2 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12091878 1551003 Tlr2 toll-like receptor 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19841034 1551003 Tlr2 toll-like receptor 2 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20407745 1551003 Tlr2 toll-like receptor 2 gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:17355971 1551003 Tlr2 toll-like receptor 2 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:14656915 1551003 Tlr2 toll-like receptor 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20407745 1551003 Tlr2 toll-like receptor 2 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:16118350 1551003 Tlr2 toll-like receptor 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11431423 1551003 Tlr2 toll-like receptor 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17118979 1551003 Tlr2 toll-like receptor 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17353199 1551003 Tlr2 toll-like receptor 2 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20407745 1551003 Tlr2 toll-like receptor 2 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:21458307 1551003 Tlr2 toll-like receptor 2 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17693552 1551003 Tlr2 toll-like receptor 2 gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17408640 1551003 Tlr2 toll-like receptor 2 gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20885960 1551003 Tlr2 toll-like receptor 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20171214 MGI PMID:28769782 1551003 Tlr2 toll-like receptor 2 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:18509040 1551003 Tlr2 toll-like receptor 2 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17355971 1551003 Tlr2 toll-like receptor 2 gene MP:0003916 decreased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:14656915 1551003 Tlr2 toll-like receptor 2 gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:19841034 1551003 Tlr2 toll-like receptor 2 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:17355971 1551003 Tlr2 toll-like receptor 2 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:18509040 1551003 Tlr2 toll-like receptor 2 gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:17707128 1551003 Tlr2 toll-like receptor 2 gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:16167081 1551003 Tlr2 toll-like receptor 2 gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:17475853 1551003 Tlr2 toll-like receptor 2 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:20885960 1551003 Tlr2 toll-like receptor 2 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:20407745 1551003 Tlr2 toll-like receptor 2 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16461338 1551003 Tlr2 toll-like receptor 2 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17135446 1551003 Tlr2 toll-like receptor 2 gene MP:0005116 abnormal circulating pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19841034 1551003 Tlr2 toll-like receptor 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16211093 1551003 Tlr2 toll-like receptor 2 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19357791 1551003 Tlr2 toll-like receptor 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20407745 1551003 Tlr2 toll-like receptor 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:14656915 1551003 Tlr2 toll-like receptor 2 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:16211093 1551003 Tlr2 toll-like receptor 2 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:18250194 1551003 Tlr2 toll-like receptor 2 gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20708624 1551003 Tlr2 toll-like receptor 2 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:14656915 1551003 Tlr2 toll-like receptor 2 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:14656915 1551003 Tlr2 toll-like receptor 2 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:20407745 1551003 Tlr2 toll-like receptor 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16244651 1551003 Tlr2 toll-like receptor 2 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:17548055 1551003 Tlr2 toll-like receptor 2 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:17693552 1551003 Tlr2 toll-like receptor 2 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:17854911 1551003 Tlr2 toll-like receptor 2 gene MP:0006080 brain ischemia IAGP N RGD:5509061 20141003 MGI PMID:19401158 1551003 Tlr2 toll-like receptor 2 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:18509040 1551003 Tlr2 toll-like receptor 2 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:17118979 1551003 Tlr2 toll-like receptor 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20885960 1551003 Tlr2 toll-like receptor 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16980352 1551003 Tlr2 toll-like receptor 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:20407745 1551003 Tlr2 toll-like receptor 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:10549626 1551003 Tlr2 toll-like receptor 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:11431423 1551003 Tlr2 toll-like receptor 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:12077222 1551003 Tlr2 toll-like receptor 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16547271 1551003 Tlr2 toll-like receptor 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18250194 1551003 Tlr2 toll-like receptor 2 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:16980352 1551003 Tlr2 toll-like receptor 2 gene MP:0008652 decreased interleukin-1 secretion IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:16547271 1551003 Tlr2 toll-like receptor 2 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:11751980 1551003 Tlr2 toll-like receptor 2 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:11431423 1551003 Tlr2 toll-like receptor 2 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:16461338 1551003 Tlr2 toll-like receptor 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:10549626 1551003 Tlr2 toll-like receptor 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:11431423 1551003 Tlr2 toll-like receptor 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:11751980 1551003 Tlr2 toll-like receptor 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:14739339 1551003 Tlr2 toll-like receptor 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:16461338 1551003 Tlr2 toll-like receptor 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:16547271 1551003 Tlr2 toll-like receptor 2 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:14739339 1551003 Tlr2 toll-like receptor 2 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16244651 1551003 Tlr2 toll-like receptor 2 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:16461338 1551003 Tlr2 toll-like receptor 2 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17707128 1551003 Tlr2 toll-like receptor 2 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16118350 1551003 Tlr2 toll-like receptor 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16244651 1551003 Tlr2 toll-like receptor 2 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17355971 1551003 Tlr2 toll-like receptor 2 gene MP:0009132 abnormal white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19841034 1551003 Tlr2 toll-like receptor 2 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19357791 1551003 Tlr2 toll-like receptor 2 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:20407745 1551003 Tlr2 toll-like receptor 2 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20170803 MGI PMID:20407745 1551003 Tlr2 toll-like receptor 2 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17353199 1551003 Tlr2 toll-like receptor 2 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15690042 1551003 Tlr2 toll-like receptor 2 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17353199 1551003 Tlr2 toll-like receptor 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19139201 1551003 Tlr2 toll-like receptor 2 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17353199 1551003 Tlr2 toll-like receptor 2 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17475877 1551003 Tlr2 toll-like receptor 2 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:18250194 1551003 Tlr2 toll-like receptor 2 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:20708624 1551003 Tlr2 toll-like receptor 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17704767 1551003 Tlr2 toll-like receptor 2 gene MP:0010266 decreased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19122641 1551003 Tlr2 toll-like receptor 2 gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19122641 1551003 Tlr2 toll-like receptor 2 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20885960 1551003 Tlr2 toll-like receptor 2 gene MP:0011077 decreased macrophage nitric oxide production IAGP N RGD:5509061 20141003 MGI PMID:11751980 1551003 Tlr2 toll-like receptor 2 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20141003 MGI PMID:11751980 1551003 Tlr2 toll-like receptor 2 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20141003 MGI PMID:15546996 1551003 Tlr2 toll-like receptor 2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:20407745 1551003 Tlr2 toll-like receptor 2 gene MP:0012320 abnormal body fat mass IAGP N RGD:5509061 20160407 MGI PMID:19841034 1551003 Tlr2 toll-like receptor 2 gene MP:0020449 decreased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:17355971 1551003 Tlr2 toll-like receptor 2 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171214 MGI PMID:28769782 1551003 Tlr2 toll-like receptor 2 gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20171214 MGI PMID:28769782 1551003 Tlr2 toll-like receptor 2 gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:14739339 1551003 Tlr2 toll-like receptor 2 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:20407745 1551003 Tlr2 toll-like receptor 2 gene MP:0031025 decreased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:14739339 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:10716933 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:9679061 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10716933 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:12556477 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10716933 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10716933 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9679061 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10716933 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12556477 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9679061 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:10716933 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:12556477 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:9679061 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10716933 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10716933 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:10716933 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12556477 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:10716933 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:9679061 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10716933 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10716933 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9679061 1551005 Mafg v-maf musculoaponeurotic fibrosarcoma oncogene family, protein G (avian) gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:10716933 1551006 Ltb lymphotoxin B gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:20226692 1551006 Ltb lymphotoxin B gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:9256477 1551006 Ltb lymphotoxin B gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:10586051 1551006 Ltb lymphotoxin B gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12070288 1551006 Ltb lymphotoxin B gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12115620 1551006 Ltb lymphotoxin B gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9133428 1551006 Ltb lymphotoxin B gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9256477 1551006 Ltb lymphotoxin B gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12115620 1551006 Ltb lymphotoxin B gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:9256477 1551006 Ltb lymphotoxin B gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20226692 1551006 Ltb lymphotoxin B gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:21436282 1551006 Ltb lymphotoxin B gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:12115620 1551006 Ltb lymphotoxin B gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:9133428 1551006 Ltb lymphotoxin B gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:9133428 1551006 Ltb lymphotoxin B gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:9133428 1551006 Ltb lymphotoxin B gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:9256477 1551006 Ltb lymphotoxin B gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:9133428 1551006 Ltb lymphotoxin B gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:9256477 1551006 Ltb lymphotoxin B gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:9256477 1551006 Ltb lymphotoxin B gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20226692 1551006 Ltb lymphotoxin B gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:12354378 1551006 Ltb lymphotoxin B gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12115620 1551006 Ltb lymphotoxin B gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:20226692 1551006 Ltb lymphotoxin B gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:10586051 1551006 Ltb lymphotoxin B gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12070288 1551006 Ltb lymphotoxin B gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12115620 1551006 Ltb lymphotoxin B gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:9133428 1551006 Ltb lymphotoxin B gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:9256477 1551006 Ltb lymphotoxin B gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9256477 1551006 Ltb lymphotoxin B gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:12115620 1551006 Ltb lymphotoxin B gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:10586051 1551006 Ltb lymphotoxin B gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:12070288 1551006 Ltb lymphotoxin B gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:12115620 1551006 Ltb lymphotoxin B gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:9133428 1551006 Ltb lymphotoxin B gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:9256477 1551006 Ltb lymphotoxin B gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12070288 1551006 Ltb lymphotoxin B gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12354378 1551006 Ltb lymphotoxin B gene MP:0008179 absent germinal center B cells IAGP N RGD:5509061 20141003 MGI PMID:10586051 1551006 Ltb lymphotoxin B gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12354378 1551006 Ltb lymphotoxin B gene MP:0008201 absent follicular dendritic cells IAGP N RGD:5509061 20141003 MGI PMID:10586051 1551006 Ltb lymphotoxin B gene MP:0008201 absent follicular dendritic cells IAGP N RGD:5509061 20141003 MGI PMID:12354378 1551006 Ltb lymphotoxin B gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:10586051 1551006 Ltb lymphotoxin B gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21436282 1551006 Ltb lymphotoxin B gene MP:0008464 absent peripheral lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10586051 1551006 Ltb lymphotoxin B gene MP:0008464 absent peripheral lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12115620 1551006 Ltb lymphotoxin B gene MP:0008464 absent peripheral lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9133428 1551006 Ltb lymphotoxin B gene MP:0008465 absent mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12354378 1551006 Ltb lymphotoxin B gene MP:0008473 abnormal spleen follicular dendritic cell network IAGP N RGD:5509061 20141003 MGI PMID:12354378 1551006 Ltb lymphotoxin B gene MP:0008473 abnormal spleen follicular dendritic cell network IAGP N RGD:5509061 20141003 MGI PMID:9256477 1551006 Ltb lymphotoxin B gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:10586051 1551006 Ltb lymphotoxin B gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:16705172 1551006 Ltb lymphotoxin B gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:12354378 1551006 Ltb lymphotoxin B gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:12354378 1551006 Ltb lymphotoxin B gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12115620 1551006 Ltb lymphotoxin B gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12115620 1551006 Ltb lymphotoxin B gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21436282 1551006 Ltb lymphotoxin B gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21436282 1551006 Ltb lymphotoxin B gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10586051 1551006 Ltb lymphotoxin B gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12070288 1551006 Ltb lymphotoxin B gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9256477 1551006 Ltb lymphotoxin B gene MP:0009628 absent brachial lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10586051 1551006 Ltb lymphotoxin B gene MP:0009628 absent brachial lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12070288 1551006 Ltb lymphotoxin B gene MP:0009628 absent brachial lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0009628 absent brachial lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9256477 1551006 Ltb lymphotoxin B gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10586051 1551006 Ltb lymphotoxin B gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12070288 1551006 Ltb lymphotoxin B gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9256477 1551006 Ltb lymphotoxin B gene MP:0009633 absent cervical lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10586051 1551006 Ltb lymphotoxin B gene MP:0009633 absent cervical lymph nodes IAGP N RGD:5509061 20170713 MGI PMID:12115620 1551006 Ltb lymphotoxin B gene MP:0009634 absent popliteal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10586051 1551006 Ltb lymphotoxin B gene MP:0009634 absent popliteal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12070288 1551006 Ltb lymphotoxin B gene MP:0009634 absent popliteal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12446781 1551006 Ltb lymphotoxin B gene MP:0009634 absent popliteal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9256477 1551006 Ltb lymphotoxin B gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12115620 1551006 Ltb lymphotoxin B gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15240709 1551006 Ltb lymphotoxin B gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20226692 1551006 Ltb lymphotoxin B gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:12446781 1551007 Ccl7 C-C motif chemokine ligand 7 gene MP:0002620 abnormal monocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17364026 1551009 Map1lc3b microtubule-associated protein 1 light chain 3 beta gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24185898 1551009 Map1lc3b microtubule-associated protein 1 light chain 3 beta gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18069693 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:19478059 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:19478059 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200402 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210128 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20240523 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:14976163 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:14976163 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0000610 cholestasis IAGP N RGD:5509061 20150326 MGI PMID:25068656 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20200402 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20150326 MGI PMID:25068656 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20200402 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0001314 cornea opacity IEA N RGD:5509061 20201231 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20201022 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220519 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14976163 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20240523 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20240523 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20231207 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20210520 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:19478059 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210128 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20150326 MGI PMID:25068656 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20150326 MGI PMID:25068656 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20150326 MGI PMID:25068656 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20240523 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20150326 MGI PMID:25068656 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20200402 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200402 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0004357 long tibia IEA N RGD:5509061 20200402 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19478059 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19478059 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:19478059 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:19478059 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20141003 MGI PMID:14976163 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20150326 MGI PMID:25068656 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:14976163 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20150326 MGI PMID:25068656 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210520 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210826 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:14976163 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:14976163 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20150326 MGI PMID:25068656 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20150326 MGI PMID:25068656 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20231207 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20231207 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20200402 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220519 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20150326 MGI PMID:25068656 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210520 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:14976163 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220519 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20200402 MGI 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:19478059 1551010 Atp8b1 ATPase, class I, type 8B, member 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210520 MGI 1551015 Exoc2 exocyst complex component 2 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20191205 MGI 1551015 Exoc2 exocyst complex component 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551015 Exoc2 exocyst complex component 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551015 Exoc2 exocyst complex component 2 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240801 MGI 1551016 Pcbd1 pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1 gene MP:0000373 belly spot IAGP N RGD:5509061 20200310 MGI PMID:12011081 1551016 Pcbd1 pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:12011081 1551016 Pcbd1 pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1 gene MP:0001304 cataract IAGP N RGD:5509061 20200310 MGI PMID:12011081 1551016 Pcbd1 pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:12011081 1551016 Pcbd1 pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1 gene MP:0002893 ketoaciduria IAGP N RGD:5509061 20200310 MGI PMID:12011081 1551016 Pcbd1 pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:12011081 1551016 Pcbd1 pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20200310 MGI PMID:12011081 1551016 Pcbd1 pterin 4 alpha carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) 1 gene MP:0030670 increased circulating phenylalanine level IAGP N RGD:5509061 20200310 MGI PMID:12011081 1551017 Mypn myopalladin gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1551017 Mypn myopalladin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:25541130 1551017 Mypn myopalladin gene MP:0000751 myopathy IAGP N RGD:5509061 20200310 MGI PMID:28017374 1551017 Mypn myopalladin gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1551017 Mypn myopalladin gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20200310 MGI PMID:25541130 1551017 Mypn myopalladin gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1551017 Mypn myopalladin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:25541130 1551017 Mypn myopalladin gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20200310 MGI PMID:25541130 1551017 Mypn myopalladin gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20200310 MGI PMID:25541130 1551017 Mypn myopalladin gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20200310 MGI PMID:25541130 1551017 Mypn myopalladin gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20200310 MGI PMID:28017374 1551017 Mypn myopalladin gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20200310 MGI PMID:25541130 1551017 Mypn myopalladin gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20200310 MGI PMID:25541130 1551017 Mypn myopalladin gene MP:0010505 abnormal T wave IAGP N RGD:5509061 20200310 MGI PMID:25541130 1551017 Mypn myopalladin gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20200310 MGI PMID:25541130 1551017 Mypn myopalladin gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20200310 MGI PMID:25541130 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18307533 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18307533 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22689267 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:22689267 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18307533 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18307533 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18307533 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18307533 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:22689267 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0003385 abnormal body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:22689267 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22689267 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22689267 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18307533 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22689267 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22689267 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:22689267 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18307533 1551018 Nuak2 NUAK family, SNF1-like kinase, 2 gene MP:0012535 abnormal optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:22689267 1551020 Sv2c synaptic vesicle glycoprotein 2c gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23458503 1551020 Sv2c synaptic vesicle glycoprotein 2c gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23458503 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20220519 MGI PMID:33961779 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20220519 MGI PMID:33961779 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20200310 MGI 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20220519 MGI PMID:33961779 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20220519 MGI PMID:33961779 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20220519 MGI PMID:33961779 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20220519 MGI PMID:33961779 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20220519 MGI PMID:33961779 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20201231 MGI 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20220519 MGI PMID:33961779 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0003036 vertebral transformation IEA N RGD:5509061 20200310 MGI 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20220519 MGI PMID:33961779 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20220519 MGI PMID:33961779 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20220519 MGI PMID:33961779 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20200310 MGI 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20200310 MGI 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20220519 MGI PMID:33961779 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0005358 abnormal incisor morphology IEA N RGD:5509061 20201022 MGI 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20220519 MGI PMID:33961779 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1551023 Aff3 AF4/FMR2 family, member 3 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220616 MGI PMID:33543287 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0001147 small testis IAGP N RGD:5509061 20220616 MGI PMID:33543287 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0001469 abnormal contextual conditioning behavior IEA N RGD:5509061 20210128 MGI 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:17060460 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0001925 male infertility IAGP N RGD:5509061 20220616 MGI PMID:33543287 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17060460 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220616 MGI PMID:33543287 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220616 MGI PMID:33543287 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220616 MGI PMID:33543287 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18347064 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220616 MGI PMID:33543287 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:17060460 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:18347064 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17060460 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17060460 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220616 MGI PMID:33543287 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17060460 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17060460 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17060460 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20220616 MGI PMID:33543287 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220616 MGI PMID:33543287 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220616 MGI PMID:33543287 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220616 MGI PMID:33543287 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18347064 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18347064 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17060460 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220616 MGI PMID:33543287 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220616 MGI PMID:33543287 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0020850 abnormal microtubule cytoskeleton morphology IAGP N RGD:5509061 20230615 MGI PMID:18347064 1551024 Ppp4c protein phosphatase 4, catalytic subunit gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20220616 MGI PMID:33543287 1551026 Dhrs1 dehydrogenase/reductase 1 gene MP:0000745 tremors IEA N RGD:5509061 20240523 MGI 1551029 Lpgat1 lysophosphatidylglycerol acyltransferase 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1551029 Lpgat1 lysophosphatidylglycerol acyltransferase 1 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20210128 MGI 1551029 Lpgat1 lysophosphatidylglycerol acyltransferase 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1551029 Lpgat1 lysophosphatidylglycerol acyltransferase 1 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1551029 Lpgat1 lysophosphatidylglycerol acyltransferase 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1551029 Lpgat1 lysophosphatidylglycerol acyltransferase 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1551029 Lpgat1 lysophosphatidylglycerol acyltransferase 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200310 MGI 1551029 Lpgat1 lysophosphatidylglycerol acyltransferase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20220519 MGI PMID:25954032 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0000161 scoliosis IAGP N RGD:5509061 20220519 MGI PMID:25954032 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0000161 scoliosis IAGP N RGD:5509061 20220519 MGI PMID:34318745 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20200310 MGI PMID:24082093 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20200310 MGI PMID:21613327 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20200310 MGI PMID:21613327 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:21613327 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20200310 MGI PMID:21613327 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:21124978 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:21613327 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:21124978 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20200310 MGI PMID:24082093 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20200310 MGI PMID:21124978 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0002188 small heart IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20200310 MGI PMID:24082093 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:21613327 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200310 MGI PMID:21124978 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0002690 akinesia IAGP N RGD:5509061 20200310 MGI PMID:21613327 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20200310 MGI PMID:21613327 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20200310 MGI PMID:24082093 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20220519 MGI PMID:25954032 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20220519 MGI PMID:34318745 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0004716 abnormal cochlear nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:21613327 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200310 MGI PMID:21613327 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20200310 MGI PMID:24082093 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0006392 abnormal nucleus pulposus morphology IAGP N RGD:5509061 20220519 MGI PMID:34318745 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20200310 MGI PMID:21124978 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:24082093 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0008958 abnormal trophoblast glycogen cell morphology IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20200310 MGI PMID:21613327 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0010038 abnormal placenta physiology IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:24082093 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21124978 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24082093 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21613327 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21613327 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0011527 disorganized placental labyrinth IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0011529 increased placenta intervillous maternal lacunae size IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20200310 MGI PMID:24082093 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20200310 MGI PMID:24082093 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0012726 abnormal uterine spiral artery morphology IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0012727 abnormal uterine spiral artery remodeling IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20220519 MGI PMID:25954032 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0020452 abnormal axon radial sorting IAGP N RGD:5509061 20200310 MGI PMID:21613327 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0030798 joint contracture IAGP N RGD:5509061 20200310 MGI PMID:21613327 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0030798 joint contracture IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0030802 abnormal tendon physiology IAGP N RGD:5509061 20220519 MGI PMID:34318745 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20230323 MGI PMID:34767447 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0031418 increased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:24082093 1551030 Adgrg6 adhesion G protein-coupled receptor G6 gene MP:0031607 abnormal fetal cardiomyocyte mitochondrial morphology IAGP N RGD:5509061 20240321 MGI PMID:24082093 1551031 Ptgdr prostaglandin D receptor gene MP:0000362 decreased mast cell histamine storage IAGP N RGD:5509061 20141003 MGI PMID:23624557 1551031 Ptgdr prostaglandin D receptor gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16624958 1551031 Ptgdr prostaglandin D receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23103473 1551031 Ptgdr prostaglandin D receptor gene MP:0001619 abnormal vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:23624557 1551031 Ptgdr prostaglandin D receptor gene MP:0001847 brain inflammation IAGP N RGD:5509061 20200702 MGI PMID:28630327 1551031 Ptgdr prostaglandin D receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16624958 1551031 Ptgdr prostaglandin D receptor gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16624958 1551031 Ptgdr prostaglandin D receptor gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:10720327 1551031 Ptgdr prostaglandin D receptor gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23624557 1551031 Ptgdr prostaglandin D receptor gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20200702 MGI PMID:28630327 1551031 Ptgdr prostaglandin D receptor gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23103473 1551031 Ptgdr prostaglandin D receptor gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20200702 MGI PMID:28630327 1551031 Ptgdr prostaglandin D receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23103473 1551031 Ptgdr prostaglandin D receptor gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:16617107 1551031 Ptgdr prostaglandin D receptor gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:16617107 1551031 Ptgdr prostaglandin D receptor gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23624557 1551031 Ptgdr prostaglandin D receptor gene MP:0008020 abnormal dermal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23624557 1551031 Ptgdr prostaglandin D receptor gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200702 MGI PMID:28630327 1551031 Ptgdr prostaglandin D receptor gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20200702 MGI PMID:28630327 1551031 Ptgdr prostaglandin D receptor gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:23624557 1551031 Ptgdr prostaglandin D receptor gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20200702 MGI PMID:28630327 1551031 Ptgdr prostaglandin D receptor gene MP:0020449 decreased microglial cell activation IAGP N RGD:5509061 20200702 MGI PMID:28630327 1551031 Ptgdr prostaglandin D receptor gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200702 MGI PMID:28630327 1551031 Ptgdr prostaglandin D receptor gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200702 MGI PMID:28630327 1551032 Ypel2 yippee like 2 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1551032 Ypel2 yippee like 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 1551032 Ypel2 yippee like 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220519 MGI 1551032 Ypel2 yippee like 2 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20200514 MGI 1551032 Ypel2 yippee like 2 gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20220519 MGI 1551032 Ypel2 yippee like 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1551032 Ypel2 yippee like 2 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1551033 Ddhd1 DDHD domain containing 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20200310 MGI 1551033 Ddhd1 DDHD domain containing 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:24599962 1551033 Ddhd1 DDHD domain containing 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220714 MGI PMID:24599962 1551033 Ddhd1 DDHD domain containing 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:24599962 1551033 Ddhd1 DDHD domain containing 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1551033 Ddhd1 DDHD domain containing 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200310 MGI 1551033 Ddhd1 DDHD domain containing 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:24599962 1551033 Ddhd1 DDHD domain containing 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20200310 MGI PMID:24599962 1551033 Ddhd1 DDHD domain containing 1 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220714 MGI PMID:24599962 1551033 Ddhd1 DDHD domain containing 1 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20220714 MGI PMID:24599962 1551033 Ddhd1 DDHD domain containing 1 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220714 MGI PMID:24599962 1551033 Ddhd1 DDHD domain containing 1 gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20220714 MGI PMID:24599962 1551033 Ddhd1 DDHD domain containing 1 gene MP:0014464 decreased sperm mitochondrial sheath size IAGP N RGD:5509061 20240613 MGI PMID:24599962 1551036 Zgpat zinc finger, CCCH-type with G patch domain gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1551036 Zgpat zinc finger, CCCH-type with G patch domain gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1551043 Parp12 poly (ADP-ribose) polymerase family, member 12 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1551043 Parp12 poly (ADP-ribose) polymerase family, member 12 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200310 MGI 1551043 Parp12 poly (ADP-ribose) polymerase family, member 12 gene MP:0001147 small testis IEA N RGD:5509061 20200310 MGI 1551043 Parp12 poly (ADP-ribose) polymerase family, member 12 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1551043 Parp12 poly (ADP-ribose) polymerase family, member 12 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 1551043 Parp12 poly (ADP-ribose) polymerase family, member 12 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1551043 Parp12 poly (ADP-ribose) polymerase family, member 12 gene MP:0005573 increased pulmonary respiratory rate IEA N RGD:5509061 20201022 MGI 1551043 Parp12 poly (ADP-ribose) polymerase family, member 12 gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 1551043 Parp12 poly (ADP-ribose) polymerase family, member 12 gene MP:0012125 decreased bronchoconstrictive response IEA N RGD:5509061 20201022 MGI 1551044 Phf7 PHD finger protein 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20210429 MGI PMID:32726616 1551044 Phf7 PHD finger protein 7 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210429 MGI PMID:32726616 1551044 Phf7 PHD finger protein 7 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20210429 MGI PMID:32726616 1551044 Phf7 PHD finger protein 7 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210429 MGI PMID:32726616 1551044 Phf7 PHD finger protein 7 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210429 MGI PMID:32726616 1551044 Phf7 PHD finger protein 7 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210429 MGI PMID:32726616 1551044 Phf7 PHD finger protein 7 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20210429 MGI PMID:32726616 1551044 Phf7 PHD finger protein 7 gene MP:0009233 enlarged sperm head IAGP N RGD:5509061 20210429 MGI PMID:32726616 1551044 Phf7 PHD finger protein 7 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20210429 MGI PMID:32726616 1551044 Phf7 PHD finger protein 7 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1551046 Gpr50 G-protein-coupled receptor 50 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17957037 1551046 Gpr50 G-protein-coupled receptor 50 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:17957037 1551046 Gpr50 G-protein-coupled receptor 50 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17957037 1551046 Gpr50 G-protein-coupled receptor 50 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17957037 1551046 Gpr50 G-protein-coupled receptor 50 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17957037 1551046 Gpr50 G-protein-coupled receptor 50 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17957037 1551046 Gpr50 G-protein-coupled receptor 50 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:17957037 1551046 Gpr50 G-protein-coupled receptor 50 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:17957037 1551047 Akap8l A kinase anchor protein 8-like gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1551047 Akap8l A kinase anchor protein 8-like gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1551047 Akap8l A kinase anchor protein 8-like gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000322 increased granulocyte number IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000373 belly spot IAGP N RGD:5509061 20200310 MGI PMID:24721909 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000373 belly spot IAGP N RGD:5509061 20200310 MGI PMID:25340873 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:24721909 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000384 distorted hair follicle pattern IAGP N RGD:5509061 20200310 MGI PMID:24721909 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000384 distorted hair follicle pattern IAGP N RGD:5509061 20200310 MGI PMID:25340873 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20200310 MGI PMID:24721909 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20200310 MGI PMID:25340873 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20200310 MGI PMID:25340873 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20200310 MGI PMID:24721909 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000592 short tail IAGP N RGD:5509061 20200310 MGI PMID:22169041 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000592 short tail IAGP N RGD:5509061 20200310 MGI PMID:25340873 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0000745 tremors IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:24721909 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0001256 abnormal body length IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0001512 trunk curl IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:22169041 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:22169041 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20200310 MGI PMID:24721909 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:22169041 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20200310 MGI PMID:25340873 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0003062 abnormal coping response IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0005015 increased T cell number IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:22169041 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20200310 MGI PMID:22169041 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20200310 MGI PMID:22169041 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20200310 MGI PMID:22169041 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0008211 decreased mature B cell number IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20200310 MGI PMID:22169041 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20200310 MGI PMID:22169041 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0008501 increased IgG2b level IEA N RGD:5509061 20200310 MGI 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20200310 MGI PMID:22169041 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20200310 MGI PMID:24721909 1551048 Mysm1 myb-like, SWIRM and MPN domains 1 gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20200310 MGI PMID:25340873 1551049 Zbtb40 zinc finger and BTB domain containing 40 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20201015 MGI PMID:32497039 1551049 Zbtb40 zinc finger and BTB domain containing 40 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20201015 MGI PMID:32497039 1551049 Zbtb40 zinc finger and BTB domain containing 40 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20201015 MGI PMID:32497039 1551049 Zbtb40 zinc finger and BTB domain containing 40 gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20201015 MGI PMID:32497039 1551049 Zbtb40 zinc finger and BTB domain containing 40 gene MP:0011585 decreased alkaline phosphatase activity IAGP N RGD:5509061 20201015 MGI PMID:32497039 1551049 Zbtb40 zinc finger and BTB domain containing 40 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20201015 MGI PMID:32497039 1551049 Zbtb40 zinc finger and BTB domain containing 40 gene MP:0013618 decreased areal bone mineral density IAGP N RGD:5509061 20201015 MGI PMID:32497039 1551049 Zbtb40 zinc finger and BTB domain containing 40 gene MP:0021190 decreased bone mineral density of lumbar vertebrae IAGP N RGD:5509061 20220915 MGI PMID:32497039 1551051 Lct lactase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1551051 Lct lactase gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0001460 abnormal olfactory discrimination memory IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0003686 abnormal eye muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0004081 abnormal globus pallidus morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0004292 abnormal spiral ligament fibrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0008265 abnormal hippocampus CA2 region morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:16014715 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551052 Man2b1 mannosidase 2, alpha B1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10400983 1551053 Zfp318 zinc finger protein 318 gene MP:0001922 reduced male fertility IEA N RGD:5509061 20141003 MGI 1551053 Zfp318 zinc finger protein 318 gene MP:0002458 abnormal B cell number IEA N RGD:5509061 20141003 MGI 1551053 Zfp318 zinc finger protein 318 gene MP:0002491 decreased IgD level IAGP N RGD:5509061 20141003 MGI PMID:24616512 1551053 Zfp318 zinc finger protein 318 gene MP:0002491 decreased IgD level IAGP N RGD:5509061 20141225 MGI PMID:25057009 1551053 Zfp318 zinc finger protein 318 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:24616512 1551053 Zfp318 zinc finger protein 318 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141225 MGI PMID:25057009 1551053 Zfp318 zinc finger protein 318 gene MP:0008191 abnormal follicular B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24616512 1551053 Zfp318 zinc finger protein 318 gene MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24616512 1551053 Zfp318 zinc finger protein 318 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:24616512 1551053 Zfp318 zinc finger protein 318 gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141225 MGI PMID:25057009 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0000032 cochlear degeneration IAGP N RGD:5509061 20141003 MGI PMID:22330676 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:22330676 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0000048 abnormal stria vascularis morphology IEA N RGD:5509061 20111116 MGI 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22105175 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:22105175 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:22105175 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:22105175 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:1728569 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:4067076 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:6541219 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:7093705 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:7432512 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:7719036 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:16648588 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:22105175 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20111116 MGI 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:1728569 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:6541219 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:6662828 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:7432512 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:7719036 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0002857 cochlear ganglion degeneration IEA N RGD:5509061 20111116 MGI 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0002894 abnormal otolith morphology IEA N RGD:5509061 20111116 MGI 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0003149 abnormal tectorial membrane morphology IEA N RGD:5509061 20111116 MGI 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0003169 abnormal scala media morphology IEA N RGD:5509061 20111116 MGI 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0003879 abnormal hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22105175 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0004300 abnormal organ of Corti supporting cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22330676 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0004302 abnormal Deiters cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22330676 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0004331 vestibular saccular macula degeneration IEA N RGD:5509061 20111116 MGI 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22105175 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22105175 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22330676 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22105175 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22330676 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20141003 MGI PMID:22105175 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0004432 abnormal cochlear hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22105175 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:22330676 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0004628 Deiters cell degeneration IEA N RGD:5509061 20111116 MGI 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:16648588 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0005307 head tossing IEA N RGD:5509061 20111116 MGI 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:22330676 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0011039 abnormal vestibuloocular dark reflex IAGP N RGD:5509061 20141003 MGI PMID:22105175 1551056 Tmc1 transmembrane channel-like gene family 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:22105175 1551060 Aaas achalasia, adrenocortical insufficiency, alacrimia gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16479006 1551060 Aaas achalasia, adrenocortical insufficiency, alacrimia gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16479006 1551060 Aaas achalasia, adrenocortical insufficiency, alacrimia gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:16479006 1551060 Aaas achalasia, adrenocortical insufficiency, alacrimia gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:16479006 1551060 Aaas achalasia, adrenocortical insufficiency, alacrimia gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16479006 1551061 Ydjc YdjC homolog (bacterial) gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1551061 Ydjc YdjC homolog (bacterial) gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1551061 Ydjc YdjC homolog (bacterial) gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1551061 Ydjc YdjC homolog (bacterial) gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1551061 Ydjc YdjC homolog (bacterial) gene MP:0002608 increased hematocrit IEA N RGD:5509061 20210826 MGI 1551061 Ydjc YdjC homolog (bacterial) gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1551061 Ydjc YdjC homolog (bacterial) gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20210826 MGI 1551061 Ydjc YdjC homolog (bacterial) gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150430 MGI 1551061 Ydjc YdjC homolog (bacterial) gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1551061 Ydjc YdjC homolog (bacterial) gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210826 MGI 1551061 Ydjc YdjC homolog (bacterial) gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1551061 Ydjc YdjC homolog (bacterial) gene MP:0008177 increased germinal center B cell number IEA N RGD:5509061 20201231 MGI 1551061 Ydjc YdjC homolog (bacterial) gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20211021 MGI 1551061 Ydjc YdjC homolog (bacterial) gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20201231 MGI 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0000315 hemoglobinuria IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20733003 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20733003 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20733003 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20733003 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0004882 enlarged lung IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0005139 increased prolactin level IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:10491259 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:20733003 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20733003 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0011567 increased renal glomerulus lobularity IAGP N RGD:5509061 20141003 MGI PMID:11287624 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:17372192 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:20733003 1551063 Mark2 MAP/microtubule affinity regulating kinase 2 gene MP:0031270 decreased susceptibility to age-related hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:17372192 1551064 Ube4a ubiquitination factor E4A gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1551064 Ube4a ubiquitination factor E4A gene MP:0002764 short tibia IEA N RGD:5509061 20210520 MGI 1551064 Ube4a ubiquitination factor E4A gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210520 MGI 1551064 Ube4a ubiquitination factor E4A gene MP:0003900 shortened QT interval IEA N RGD:5509061 20220519 MGI 1551064 Ube4a ubiquitination factor E4A gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210520 MGI 1551064 Ube4a ubiquitination factor E4A gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210520 MGI 1551064 Ube4a ubiquitination factor E4A gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210520 MGI 1551064 Ube4a ubiquitination factor E4A gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 1551067 Mlycd malonyl-CoA decarboxylase gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17030679 1551067 Mlycd malonyl-CoA decarboxylase gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:17030679 1551067 Mlycd malonyl-CoA decarboxylase gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:17030679 1551069 Tmem30b transmembrane protein 30B gene MP:0000274 enlarged heart IEA N RGD:5509061 20200310 MGI 1551069 Tmem30b transmembrane protein 30B gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20200310 MGI 1551069 Tmem30b transmembrane protein 30B gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200310 MGI 1551069 Tmem30b transmembrane protein 30B gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200310 MGI 1551069 Tmem30b transmembrane protein 30B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1551071 Prokr1 prokineticin receptor 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18421008 1551071 Prokr1 prokineticin receptor 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220519 MGI 1551071 Prokr1 prokineticin receptor 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:18421008 1551071 Prokr1 prokineticin receptor 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:16793879 1551071 Prokr1 prokineticin receptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16537498 1551071 Prokr1 prokineticin receptor 1 gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20141003 MGI PMID:16793879 1551071 Prokr1 prokineticin receptor 1 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:16793879 1551071 Prokr1 prokineticin receptor 1 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:16793879 1551071 Prokr1 prokineticin receptor 1 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:16793879 1551071 Prokr1 prokineticin receptor 1 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:16793879 1551071 Prokr1 prokineticin receptor 1 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:16793879 1551071 Prokr1 prokineticin receptor 1 gene MP:0011947 abnormal fluid intake IAGP N RGD:5509061 20141003 MGI PMID:16793879 1551071 Prokr1 prokineticin receptor 1 gene MP:0020329 decreased capillary density IAGP N RGD:5509061 20160714 MGI PMID:18421008 1551072 Ctrb1 chymotrypsinogen B1 gene MP:0001785 edema IAGP N RGD:5509061 20200924 MGI PMID:30076839 1551072 Ctrb1 chymotrypsinogen B1 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20200924 MGI PMID:32678161 1551072 Ctrb1 chymotrypsinogen B1 gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20200924 MGI PMID:30076839 1551072 Ctrb1 chymotrypsinogen B1 gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20200924 MGI PMID:30076839 1551072 Ctrb1 chymotrypsinogen B1 gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20200924 MGI PMID:32678161 1551072 Ctrb1 chymotrypsinogen B1 gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20200924 MGI PMID:30076839 1551074 Lingo2 leucine rich repeat and Ig domain containing 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 1551074 Lingo2 leucine rich repeat and Ig domain containing 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 1551074 Lingo2 leucine rich repeat and Ig domain containing 2 gene MP:0001257 increased body length IEA N RGD:5509061 20230601 MGI 1551074 Lingo2 leucine rich repeat and Ig domain containing 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20230601 MGI 1551074 Lingo2 leucine rich repeat and Ig domain containing 2 gene MP:0004357 long tibia IEA N RGD:5509061 20230601 MGI 1551074 Lingo2 leucine rich repeat and Ig domain containing 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20230601 MGI 1551074 Lingo2 leucine rich repeat and Ig domain containing 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230601 MGI 1551074 Lingo2 leucine rich repeat and Ig domain containing 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230601 MGI 1551080 Ccl22 C-C motif chemokine ligand 22 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20170615 MGI PMID:27195186 1551080 Ccl22 C-C motif chemokine ligand 22 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551081 Txndc2 thioredoxin domain containing 2 (spermatozoa) gene MP:0001257 increased body length IEA N RGD:5509061 20111116 MGI 1551081 Txndc2 thioredoxin domain containing 2 (spermatozoa) gene MP:0001260 increased body weight IEA N RGD:5509061 20111116 MGI 1551081 Txndc2 thioredoxin domain containing 2 (spermatozoa) gene MP:0001264 increased body size IEA N RGD:5509061 20111116 MGI 1551081 Txndc2 thioredoxin domain containing 2 (spermatozoa) gene MP:0001565 abnormal circulating phosphate level IEA N RGD:5509061 20111116 MGI 1551081 Txndc2 thioredoxin domain containing 2 (spermatozoa) gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23707457 1551081 Txndc2 thioredoxin domain containing 2 (spermatozoa) gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23707457 1551081 Txndc2 thioredoxin domain containing 2 (spermatozoa) gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:23707457 1551081 Txndc2 thioredoxin domain containing 2 (spermatozoa) gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:23707457 1551081 Txndc2 thioredoxin domain containing 2 (spermatozoa) gene MP:0008597 decreased circulating interleukin-6 level IEA N RGD:5509061 20111116 MGI 1551081 Txndc2 thioredoxin domain containing 2 (spermatozoa) gene MP:0012582 increased peroxidase activity IAGP N RGD:5509061 20141003 MGI PMID:23707457 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0000381 enlarged hair follicles IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:12101409 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23755247 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001163 abnormal prostate gland anterior lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:23755247 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:18599506 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001306 small lens IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001320 small pupil IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001346 abnormal lacrimal gland morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:18983969 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20220303 MGI PMID:22233806 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20220303 MGI PMID:22233806 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220303 MGI PMID:22233806 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20220303 MGI PMID:22233806 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220303 MGI PMID:22233806 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:18599506 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23755247 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:18599506 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0002274 abnormal type I pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18599506 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18599506 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0002579 disorganized secondary lens fibers IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:20980403 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:18983969 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:23755247 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0003671 abnormal eyelid aperture IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:20980403 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220303 MGI PMID:22233806 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0004481 abnormal conjunctival epithelium morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:12101409 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:18599506 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18395082 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:12101409 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0004962 decreased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:23755247 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:18395082 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18983969 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0005247 abnormal extraocular muscle morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:12101409 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12101409 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0006167 eyelid edema IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:12101409 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20181011 MGI 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0009381 abnormal prostate gland dorsolateral lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:23755247 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0009662 abnormal uterine receptivity IAGP N RGD:5509061 20220303 MGI PMID:22233806 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20220303 MGI PMID:22233806 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0009742 increased cornea stroma thickness IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:12101409 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0009935 abnormal Meibomian gland acinus morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0010814 absent alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:18599506 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0010816 decreased type I pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:18599506 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:18599506 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0010894 pulmonary alveolar edema IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18599506 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12101409 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18983969 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20980403 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:18599506 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0011163 increased wet-to-dry lung weight ratio IAGP N RGD:5509061 20141003 MGI PMID:20038803 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0011482 posterior iris synechia IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:20980403 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0012117 decreased trophectoderm cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20980403 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0013385 abnormal Meibomian gland development IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0013391 abnormal Meibomian gland physiology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0013394 abnormal palpebral conjunctiva morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0013527 absent conjunctiva goblet cells IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0013754 abnormal ocular surface morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0014147 lacrimal gland necrosis IAGP N RGD:5509061 20160407 MGI PMID:21600198 1551083 Klf5 Kruppel-like transcription factor 5 gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:21600198 1551084 Zbp1 Z-DNA binding protein 1 gene MP:0012555 decreased cell death IAGP N RGD:5509061 20180125 MGI PMID:28716805 1551084 Zbp1 Z-DNA binding protein 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20150219 MGI PMID:24557836 1551084 Zbp1 Z-DNA binding protein 1 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:28716805 1551086 Camta1 calmodulin binding transcription activator 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:25049392 1551086 Camta1 calmodulin binding transcription activator 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20200310 MGI PMID:25049392 1551086 Camta1 calmodulin binding transcription activator 1 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20200310 MGI PMID:25049392 1551086 Camta1 calmodulin binding transcription activator 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:25049392 1551086 Camta1 calmodulin binding transcription activator 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:25049392 1551086 Camta1 calmodulin binding transcription activator 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:25049392 1551086 Camta1 calmodulin binding transcription activator 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20200310 MGI PMID:25049392 1551086 Camta1 calmodulin binding transcription activator 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20200310 MGI PMID:25049392 1551086 Camta1 calmodulin binding transcription activator 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25049392 1551086 Camta1 calmodulin binding transcription activator 1 gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20200310 MGI PMID:25049392 1551086 Camta1 calmodulin binding transcription activator 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25049392 1551086 Camta1 calmodulin binding transcription activator 1 gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20200310 MGI PMID:25049392 1551089 Cmpk1 cytidine/uridine monophosphate kinase 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1551089 Cmpk1 cytidine/uridine monophosphate kinase 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20200310 MGI 1551089 Cmpk1 cytidine/uridine monophosphate kinase 1 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1551089 Cmpk1 cytidine/uridine monophosphate kinase 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1551089 Cmpk1 cytidine/uridine monophosphate kinase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551092 Ctu2 cytosolic thiouridylase subunit 2 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1551092 Ctu2 cytosolic thiouridylase subunit 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1551092 Ctu2 cytosolic thiouridylase subunit 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551093 Zranb1 zinc finger, RAN-binding domain containing 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230413 MGI PMID:36087511 1551093 Zranb1 zinc finger, RAN-binding domain containing 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230413 MGI PMID:36087511 1551093 Zranb1 zinc finger, RAN-binding domain containing 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20200310 MGI PMID:26808229 1551093 Zranb1 zinc finger, RAN-binding domain containing 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1551093 Zranb1 zinc finger, RAN-binding domain containing 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200310 MGI PMID:26808229 1551093 Zranb1 zinc finger, RAN-binding domain containing 1 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20201022 MGI 1551093 Zranb1 zinc finger, RAN-binding domain containing 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:26808229 1551093 Zranb1 zinc finger, RAN-binding domain containing 1 gene MP:0008087 decreased T helper 1 cell number IAGP N RGD:5509061 20200310 MGI PMID:26808229 1551093 Zranb1 zinc finger, RAN-binding domain containing 1 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20200310 MGI PMID:26808229 1551093 Zranb1 zinc finger, RAN-binding domain containing 1 gene MP:0008615 decreased circulating interleukin-17 level IAGP N RGD:5509061 20200310 MGI PMID:26808229 1551093 Zranb1 zinc finger, RAN-binding domain containing 1 gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20200310 MGI PMID:26808229 1551093 Zranb1 zinc finger, RAN-binding domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551093 Zranb1 zinc finger, RAN-binding domain containing 1 gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20230413 MGI PMID:36087511 1551093 Zranb1 zinc finger, RAN-binding domain containing 1 gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20230413 MGI PMID:36087511 1551093 Zranb1 zinc finger, RAN-binding domain containing 1 gene MP:0014219 decreased intestinal mucosa thickness IAGP N RGD:5509061 20230413 MGI PMID:36087511 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10702415 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:10518539 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:7603567 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:10518539 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15199130 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:15199130 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000380 small hair follicles IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:15199130 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000384 distorted hair follicle pattern IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18250470 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:11160181 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:18250470 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17096024 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:9120401 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9120401 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:10702415 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:18299349 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10433815 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15199130 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:15199130 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001220 epidermal necrosis IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:15199130 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10702415 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:18408078 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:18408078 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:18408078 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10518539 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7603567 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:10702415 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15199130 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:9120401 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:10702415 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:10702415 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:10702415 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17525802 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:17525802 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:18408078 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18250470 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18408078 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:18408078 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19263497 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:10702415 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11160181 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21419662 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15199130 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:18250470 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0002814 hyperchromasia IAGP N RGD:5509061 20141003 MGI PMID:10518539 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15199130 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:7603567 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10433815 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:11160181 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:11160181 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15905096 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17525802 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10518539 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16485035 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18408078 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:7603567 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17096024 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:9120401 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:10433815 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18250470 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:11160181 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:18250470 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9120401 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9120401 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9120401 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:18250470 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008112 abnormal monocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:10518539 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11869686 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:11869686 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:11034607 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008343 abnormal gamma-delta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21419662 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:10702415 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18250470 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9120401 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:18250470 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:21419662 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:18606991 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:17525802 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17525802 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18250470 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:10518539 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:18299349 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0009405 increased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:18299349 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20141003 MGI PMID:11160181 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17525802 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18250470 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10702415 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15199130 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10518539 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10518539 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17101783 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18408078 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7603567 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9120401 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15199130 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18408078 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18408078 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17101783 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0020854 increased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:20713516 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0030582 abnormal hair follicle placode formation IAGP N RGD:5509061 20180614 MGI PMID:15199130 1551095 Rela v-rel reticuloendotheliosis viral oncogene homolog A (avian) gene MP:0031319 impaired intestine regeneration IAGP N RGD:5509061 20211125 MGI PMID:18250470 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20200702 MGI PMID:26136579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22586041 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20200702 MGI PMID:26136579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20200702 MGI PMID:26136579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17408640 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20220616 MGI PMID:33343574 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0000753 paralysis IAGP N RGD:5509061 20200702 MGI PMID:26136579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0000921 demyelination IAGP N RGD:5509061 20200702 MGI PMID:26136579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19808018 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19808018 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19357791 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:16832055 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17456769 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:18492657 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17357057 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17707128 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19808018 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:17626835 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002334 abnormal airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:17626835 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12447442 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16461338 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16625202 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17159982 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17486093 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18656388 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21760953 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16832055 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23334413 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:16832055 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20200423 MGI PMID:19079579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:16832055 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:16832055 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12447442 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15800576 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12447442 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12872135 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16832055 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17118979 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17159982 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18776906 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:21760953 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200702 MGI PMID:26136579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:18656388 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17158234 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16703567 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20220616 MGI PMID:33343574 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:23334413 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16703567 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19808018 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19808018 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:22586041 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:22586041 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:14993594 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15034168 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17118979 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17159982 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20855887 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200423 MGI PMID:19079579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:21458307 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17408640 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:19218085 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19357791 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:17591966 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20200702 MGI PMID:26136579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20200702 MGI PMID:26136579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:17475853 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0004242 abnormal plasmacytoid dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17723216 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:20526283 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:19668221 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16440059 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20220616 MGI PMID:33343574 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:19808018 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16703567 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17456769 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17135446 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17082622 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12447442 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20220616 MGI PMID:33343574 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22586041 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19357791 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:22586041 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20150305 MGI PMID:24439266 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20200702 MGI PMID:26136579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20150305 MGI PMID:24439266 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:22586041 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19808018 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16244651 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18981228 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0006334 abnormal susceptibility to hearing loss IAGP N RGD:5509061 20141003 MGI PMID:17357057 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14993594 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20150305 MGI PMID:24439266 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18656388 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20220616 MGI PMID:33343574 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18656388 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:17135446 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20220616 MGI PMID:33343574 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16703567 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18656388 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:18492657 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:18656388 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:18492657 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16703567 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20530205 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20855887 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22586041 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:18641654 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:12872135 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17135446 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17159982 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17456769 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22586041 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22851711 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:15800576 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:17723216 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20200423 MGI PMID:16985170 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16461338 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17135446 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23334413 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20200702 MGI PMID:26136579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:22586041 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18656388 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:22586041 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008648 decreased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:18656388 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008648 decreased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:22586041 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:16407889 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:22586041 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:17159982 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:16461338 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:17135446 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:16461338 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17456769 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17525287 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20855887 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:22586041 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:22851711 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:21760953 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:22586041 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16244651 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:18776906 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:16625202 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16204620 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17707128 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20220616 MGI PMID:33343574 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16244651 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20855887 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20530205 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20141003 MGI PMID:18656388 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0008906 abnormal parametrial fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:19808018 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:19357791 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19357791 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19808018 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19808018 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20141003 MGI PMID:21804564 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17704767 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19808018 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20210204 MGI PMID:22586041 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0010222 abnormal T-helper 17 cell physiology IAGP N RGD:5509061 20150305 MGI PMID:24439266 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0010266 decreased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16204620 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20141003 MGI PMID:21998396 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0010750 increased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17082622 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14993594 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18656388 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:23179078 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0010845 decreased effector memory CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200702 MGI PMID:26136579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0011077 decreased macrophage nitric oxide production IAGP N RGD:5509061 20141003 MGI PMID:17082622 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20141003 MGI PMID:17082622 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:19808018 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20150312 MGI PMID:21804564 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0020186 abnormal susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:22851711 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:14993594 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:16832055 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:15800576 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16625202 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:19079579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200702 MGI PMID:26136579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:19079579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200702 MGI PMID:26136579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0031054 bronchiolitis IAGP N RGD:5509061 20200709 MGI PMID:19079579 1551097 Myd88 myeloid differentiation primary response gene 88 gene MP:0031225 decreased CXCL10 level IAGP N RGD:5509061 20210204 MGI PMID:22586041 1551102 Bpi bactericidal permeablility increasing protein gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20240509 MGI PMID:38457343 1551102 Bpi bactericidal permeablility increasing protein gene MP:0005015 increased T cell number IAGP N RGD:5509061 20240509 MGI PMID:38457343 1551102 Bpi bactericidal permeablility increasing protein gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20240509 MGI PMID:38457343 1551102 Bpi bactericidal permeablility increasing protein gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20240509 MGI PMID:38457343 1551102 Bpi bactericidal permeablility increasing protein gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20240509 MGI PMID:38457343 1551102 Bpi bactericidal permeablility increasing protein gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20240509 MGI PMID:38457343 1551102 Bpi bactericidal permeablility increasing protein gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20240509 MGI PMID:38457343 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0002450 abnormal lymph organ development IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0003385 abnormal body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0010146 umbilical hernia IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0010426 abnormal heart and great artery attachment IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0010439 abnormal hepatic vein morphology IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0010912 herniated liver IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0012269 nuchal edema IAGP N RGD:5509061 20141003 MGI PMID:22538705 1551104 Nprl3 nitrogen permease regulator-like 3 gene MP:0014519 myocardial ventricular hypertrabeculation IAGP N RGD:5509061 20240822 MGI PMID:22538705 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170105 MGI 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0001147 small testis IEA N RGD:5509061 20170105 MGI 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18794888 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18794888 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18794888 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20201022 MGI 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170105 MGI 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0003064 decreased coping response IAGP N RGD:5509061 20141003 MGI PMID:18794888 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:18794888 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18794888 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:18794888 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20170105 MGI 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18794888 1551107 Slitrk1 SLIT and NTRK-like family, member 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18794888 1551109 Smpdl3a sphingomyelin phosphodiesterase, acid-like 3A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1551109 Smpdl3a sphingomyelin phosphodiesterase, acid-like 3A gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14729950 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:8096198 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:8096198 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8096198 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14978099 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:8096198 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14978099 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:14978099 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:14978099 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:14729950 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:8096198 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:8096198 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:8096198 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14729950 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14978099 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8096198 1551110 Pou2f2 POU domain, class 2, transcription factor 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14729950 1551114 Calcoco1 calcium binding and coiled coil domain 1 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20240523 MGI 1551114 Calcoco1 calcium binding and coiled coil domain 1 gene MP:0001304 cataract IEA N RGD:5509061 20220519 MGI 1551114 Calcoco1 calcium binding and coiled coil domain 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210826 MGI 1551114 Calcoco1 calcium binding and coiled coil domain 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201022 MGI 1551114 Calcoco1 calcium binding and coiled coil domain 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20210826 MGI 1551114 Calcoco1 calcium binding and coiled coil domain 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210826 MGI 1551114 Calcoco1 calcium binding and coiled coil domain 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 1551114 Calcoco1 calcium binding and coiled coil domain 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210826 MGI 1551117 Zfp407 zinc finger protein 407 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1551117 Zfp407 zinc finger protein 407 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20240926 MGI 1551117 Zfp407 zinc finger protein 407 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20201022 MGI 1551117 Zfp407 zinc finger protein 407 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20191205 MGI 1551117 Zfp407 zinc finger protein 407 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20191205 MGI 1551117 Zfp407 zinc finger protein 407 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551117 Zfp407 zinc finger protein 407 gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20191205 MGI 1551117 Zfp407 zinc finger protein 407 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551119 Ttc9 tetratricopeptide repeat domain 9 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20200310 MGI PMID:25798063 1551119 Ttc9 tetratricopeptide repeat domain 9 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:25798063 1551119 Ttc9 tetratricopeptide repeat domain 9 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:25798063 1551119 Ttc9 tetratricopeptide repeat domain 9 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20200310 MGI PMID:25798063 1551119 Ttc9 tetratricopeptide repeat domain 9 gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20200310 MGI PMID:25798063 1551120 Rbm19 RNA binding motif protein 19 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:19087264 1551120 Rbm19 RNA binding motif protein 19 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:19087264 1551120 Rbm19 RNA binding motif protein 19 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20200310 MGI PMID:19087264 1551120 Rbm19 RNA binding motif protein 19 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19087264 1551120 Rbm19 RNA binding motif protein 19 gene MP:0012111 failure of morula compaction IAGP N RGD:5509061 20200310 MGI PMID:19087264 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18490740 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19171887 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18490740 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20150226 MGI PMID:18490740 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:18490740 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23602766 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18490740 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:23602766 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:23602766 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18490740 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:23602766 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0005398 decreased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:19171887 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:18490740 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23602766 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23602766 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0008559 abnormal interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23602766 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18490740 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19171887 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23602766 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0008615 decreased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:23602766 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:19171887 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0008680 abnormal interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:23602766 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:19171887 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:19171887 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:23602766 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23602766 1551121 Clec4e C-type lectin domain family 4, member e gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23602766 1551124 Cab39l calcium binding protein 39-like gene MP:0000274 enlarged heart IEA N RGD:5509061 20200310 MGI 1551124 Cab39l calcium binding protein 39-like gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20240801 MGI PMID:38676926 1551124 Cab39l calcium binding protein 39-like gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1551124 Cab39l calcium binding protein 39-like gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20240801 MGI PMID:38676926 1551126 Rbm26 RNA binding motif protein 26 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11940672 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:11940672 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11940672 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16672719 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:11940672 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0001717 absent ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16672719 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16672719 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11857798 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:11940672 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:11940672 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0003954 abnormal Reichert's membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11940672 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11940672 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16672719 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0011200 abnormal extraembryonic coelom morphology IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551127 Tfap2c transcription factor AP-2, gamma gene MP:0011207 absent ectoplacental cavity IAGP N RGD:5509061 20141003 MGI PMID:12015300 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20191128 MGI PMID:28194446 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20191128 MGI PMID:28194446 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20141003 MGI 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20191128 MGI PMID:28194446 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20141003 MGI 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20170105 MGI 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000678 abnormal parathyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17694176 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:16847339 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21357625 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0001562 abnormal circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20191128 MGI PMID:28194446 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16847339 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16847339 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:16847339 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002249 abnormal larynx morphology IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17482476 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:21357625 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11689889 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18084302 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20141003 MGI 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20170105 MGI 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002876 abnormal thyroid gland physiology IAGP N RGD:5509061 20141003 MGI PMID:17694176 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20191128 MGI PMID:28194446 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0002985 abnormal urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:18084302 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:19171764 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210128 MGI 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:17694176 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:16847339 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:16847339 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:11689889 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20170105 MGI 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0004697 abnormal thyroid follicular cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17694176 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18084302 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20161027 MGI PMID:26168216 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20141003 MGI 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17694176 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20141003 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:12533510 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:17694176 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160804 MGI 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20161027 MGI PMID:26168216 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:19171764 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20141003 MGI 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21357625 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0010326 malleus hypoplasia IAGP N RGD:5509061 20170928 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0010432 common ventricle IAGP N RGD:5509061 20141003 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0010640 ventricular myocardium compact layer hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20191128 MGI PMID:28194446 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11689889 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20191128 MGI PMID:28194446 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20191128 MGI PMID:28194446 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20191128 MGI PMID:28194446 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0012045 increased susceptibility to hypertension IAGP N RGD:5509061 20161027 MGI PMID:26168216 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20191128 MGI PMID:28194446 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0020106 decreased nitrate level IAGP N RGD:5509061 20161027 MGI PMID:26168216 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:16988000 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0030107 incus hypoplasia IAGP N RGD:5509061 20170928 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0030128 stapes hypoplasia IAGP N RGD:5509061 20170928 MGI PMID:9687499 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0030299 lower jaw to upper jaw transformation IAGP N RGD:5509061 20171102 MGI PMID:18199583 1551128 Gna11 guanine nucleotide binding protein, alpha 11 gene MP:0030884 rachitic rosary IAGP N RGD:5509061 20181101 MGI PMID:16988000 1551129 Lman2 lectin, mannose-binding 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240523 MGI 1551129 Lman2 lectin, mannose-binding 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20240523 MGI 1551130 Atp6v1g2 ATPase, H+ transporting, lysosomal V1 subunit G2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1551132 Mageh1 MAGE family member H1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240523 MGI 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0009837 abnormal sperm end piece morphology IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20200310 MGI PMID:30929735 1551133 Ttc21a tetratricopeptide repeat domain 21A gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20220811 MGI PMID:30929735 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20210304 MGI PMID:32966787 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0000248 macrocytosis IAGP N RGD:5509061 20210304 MGI PMID:32966787 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20210304 MGI PMID:32966787 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20210304 MGI PMID:32966787 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20210304 MGI PMID:32966787 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0002872 polycythemia IAGP N RGD:5509061 20210304 MGI PMID:32966787 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20210304 MGI PMID:32966787 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20210304 MGI PMID:32966787 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20210304 MGI PMID:32966787 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0010751 decreased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20210304 MGI PMID:32966787 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20210304 MGI PMID:32966787 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0011236 increased blood oxygen capacity IAGP N RGD:5509061 20210304 MGI PMID:32966787 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20210304 MGI PMID:32966787 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0011913 abnormal reticulocyte cell number IAGP N RGD:5509061 20210304 MGI PMID:32966787 1551134 Bpgm 2,3-bisphosphoglycerate mutase gene MP:0031276 abnormal stress erythropoiesis IAGP N RGD:5509061 20210805 MGI PMID:32966787 1551135 Nsd3 nuclear receptor binding SET domain protein 3 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201231 MGI 1551135 Nsd3 nuclear receptor binding SET domain protein 3 gene MP:0000692 small spleen IEA N RGD:5509061 20181227 MGI 1551135 Nsd3 nuclear receptor binding SET domain protein 3 gene MP:0000745 tremors IEA N RGD:5509061 20160421 MGI 1551135 Nsd3 nuclear receptor binding SET domain protein 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1551135 Nsd3 nuclear receptor binding SET domain protein 3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20170105 MGI 1551135 Nsd3 nuclear receptor binding SET domain protein 3 gene MP:0001512 trunk curl IEA N RGD:5509061 20160421 MGI 1551135 Nsd3 nuclear receptor binding SET domain protein 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1551135 Nsd3 nuclear receptor binding SET domain protein 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1551135 Nsd3 nuclear receptor binding SET domain protein 3 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20240613 MGI PMID:29101251 1551135 Nsd3 nuclear receptor binding SET domain protein 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551135 Nsd3 nuclear receptor binding SET domain protein 3 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20240613 MGI PMID:29101251 1551135 Nsd3 nuclear receptor binding SET domain protein 3 gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20240613 MGI PMID:29101251 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20190221 MGI PMID:24814481 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20190221 MGI PMID:24814481 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20190221 MGI PMID:24814481 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20190221 MGI PMID:24814481 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20190221 MGI PMID:24814481 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0014173 increased fatty acid beta-oxidation IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0020521 browned white adipose tissue morphology IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20190228 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:26997277 1551139 Abhd6 abhydrolase domain containing 6 gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:26997277 1551140 Marchf7 membrane associated ring-CH-type finger 7 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20200310 MGI PMID:15670816 1551140 Marchf7 membrane associated ring-CH-type finger 7 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20200310 MGI PMID:15670816 1551140 Marchf7 membrane associated ring-CH-type finger 7 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200310 MGI PMID:15670816 1551140 Marchf7 membrane associated ring-CH-type finger 7 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200310 MGI PMID:15670816 1551140 Marchf7 membrane associated ring-CH-type finger 7 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:15670816 1551140 Marchf7 membrane associated ring-CH-type finger 7 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20200310 MGI PMID:15670816 1551140 Marchf7 membrane associated ring-CH-type finger 7 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20200310 MGI PMID:15670816 1551141 Cryba2 crystallin, beta A2 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:21212184 1551141 Cryba2 crystallin, beta A2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:21212184 1551141 Cryba2 crystallin, beta A2 gene MP:0010251 subcapsular cataract IAGP N RGD:5509061 20141003 MGI PMID:21212184 1551141 Cryba2 crystallin, beta A2 gene MP:0010263 total cataract IAGP N RGD:5509061 20141003 MGI PMID:21212184 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:15687236 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:18449193 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18449193 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10196176 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:22370636 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20160421 MGI PMID:22666336 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:22214849 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:23873941 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:23873941 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:16625210 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001260 increased body weight IAGP N RGD:5509061 20220317 MGI PMID:28357399 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16625210 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17540175 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:16625210 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18449193 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:10196176 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10196176 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:15687236 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18449193 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16625210 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17540175 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10196176 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001925 male infertility IAGP N RGD:5509061 20220317 MGI PMID:28357399 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20220317 MGI PMID:28357399 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20160421 MGI PMID:22666336 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:17540175 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15713620 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16625210 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22214849 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0002083 premature death IAGP N RGD:5509061 20160421 MGI PMID:22666336 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:22214849 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20220317 MGI PMID:28357399 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20220317 MGI PMID:28357399 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18449193 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19597047 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19597047 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15687236 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20141003 MGI PMID:22214849 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:16625210 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20160421 MGI PMID:22666336 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20220317 MGI PMID:28357399 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:16625210 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:15687236 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16625210 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18449193 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:18449193 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16625210 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:19597047 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17540175 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15687236 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:18449193 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:16625210 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22214849 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220317 MGI PMID:28357399 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220317 MGI PMID:28357399 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15687236 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19597047 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20220317 MGI PMID:28357399 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15713620 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16625210 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:16625210 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17060635 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18594509 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16625210 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20220317 MGI PMID:28357399 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20220317 MGI PMID:28357399 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:16625210 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22722829 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0006422 increased mammary adenoacanthoma incidence IAGP N RGD:5509061 20160421 MGI PMID:22666336 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22214849 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20200109 MGI PMID:25742742 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17540175 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0008940 delayed balanopreputial separation IAGP N RGD:5509061 20220317 MGI PMID:28357399 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0009216 abnormal peritoneum morphology IAGP N RGD:5509061 20141003 MGI PMID:22214849 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:18594509 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22214849 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0009469 increased skin hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23873941 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20160421 MGI PMID:22666336 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20160421 MGI PMID:22666336 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0009715 thick epidermis stratum basale IAGP N RGD:5509061 20141003 MGI PMID:23873941 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0009819 abnormal circulating androgen level IAGP N RGD:5509061 20220317 MGI PMID:28357399 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20220317 MGI PMID:28357399 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0010173 increased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20160421 MGI PMID:22666336 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17540175 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22370636 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20160421 MGI PMID:22666336 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0010364 increased fibroadenoma incidence IAGP N RGD:5509061 20160421 MGI PMID:22666336 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:19597047 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17540175 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17540175 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18449193 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10196176 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15687236 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16625210 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18449193 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22214849 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0012080 chylous ascites IAGP N RGD:5509061 20141003 MGI PMID:17540175 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200109 MGI PMID:25742742 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18449193 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22214849 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0012732 abnormal perineural vascular plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:18449193 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20141003 MGI PMID:22214849 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:22214849 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0013778 abnormal mammary gland myoepithelium morphology IAGP N RGD:5509061 20160421 MGI PMID:22666336 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0013782 abnormal mammary duct terminal end bud morphology IAGP N RGD:5509061 20160421 MGI PMID:22666336 1551142 Pik3ca phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha gene MP:0014057 abnormal mammary gland stroma morphology IAGP N RGD:5509061 20160421 MGI PMID:22666336 1551143 Phkg1 phosphorylase kinase gamma 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 1551143 Phkg1 phosphorylase kinase gamma 1 gene MP:0000601 small liver IEA N RGD:5509061 20220519 MGI 1551143 Phkg1 phosphorylase kinase gamma 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 1551143 Phkg1 phosphorylase kinase gamma 1 gene MP:0001304 cataract IEA N RGD:5509061 20220519 MGI 1551143 Phkg1 phosphorylase kinase gamma 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 1551143 Phkg1 phosphorylase kinase gamma 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1551143 Phkg1 phosphorylase kinase gamma 1 gene MP:0002989 small kidney IEA N RGD:5509061 20220519 MGI 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:19037259 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19037259 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0000960 abnormal sensory ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19037259 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0001393 ataxia IEA N RGD:5509061 20111116 MGI 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:19037259 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:19037259 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0002183 gliosis IEA N RGD:5509061 20111116 MGI 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:19037259 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:23047693 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:19037259 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19037259 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:19037259 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0012503 increased midbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0012504 increased forebrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0020851 abnormal vacuole morphology IAGP N RGD:5509061 20230615 MGI PMID:17956977 1551146 Vac14 Vac14 homolog (S. cerevisiae) gene MP:0021002 brain lesion IAGP N RGD:5509061 20210805 MGI PMID:17956977 1551147 Lama5 laminin, alpha 5 gene MP:0000024 lowered ear position IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0000075 absent neurocranium IAGP N RGD:5509061 20141003 MGI PMID:9852162 1551147 Lama5 laminin, alpha 5 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:16365040 1551147 Lama5 laminin, alpha 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15936333 1551147 Lama5 laminin, alpha 5 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20220428 MGI PMID:28735299 1551147 Lama5 laminin, alpha 5 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:16365040 1551147 Lama5 laminin, alpha 5 gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:9852162 1551147 Lama5 laminin, alpha 5 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:12921739 1551147 Lama5 laminin, alpha 5 gene MP:0000484 abnormal pulmonary artery morphology IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12921739 1551147 Lama5 laminin, alpha 5 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20220428 MGI PMID:28735299 1551147 Lama5 laminin, alpha 5 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:10625553 1551147 Lama5 laminin, alpha 5 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:10625553 1551147 Lama5 laminin, alpha 5 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:9852162 1551147 Lama5 laminin, alpha 5 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0000650 mesocardia IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:18794334 1551147 Lama5 laminin, alpha 5 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:16365040 1551147 Lama5 laminin, alpha 5 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9852162 1551147 Lama5 laminin, alpha 5 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:9852162 1551147 Lama5 laminin, alpha 5 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:18794334 1551147 Lama5 laminin, alpha 5 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:18794334 1551147 Lama5 laminin, alpha 5 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:16365040 1551147 Lama5 laminin, alpha 5 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:15936333 1551147 Lama5 laminin, alpha 5 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15936333 1551147 Lama5 laminin, alpha 5 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:15936333 1551147 Lama5 laminin, alpha 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16790509 1551147 Lama5 laminin, alpha 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18794334 1551147 Lama5 laminin, alpha 5 gene MP:0001293 anophthalmia IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0001297 microphthalmia IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15936333 1551147 Lama5 laminin, alpha 5 gene MP:0001697 abnormal embryo size IAGP N RGD:5509061 20141003 MGI PMID:16365040 1551147 Lama5 laminin, alpha 5 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:9852162 1551147 Lama5 laminin, alpha 5 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20150535 1551147 Lama5 laminin, alpha 5 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:15936333 1551147 Lama5 laminin, alpha 5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15936333 1551147 Lama5 laminin, alpha 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16790509 1551147 Lama5 laminin, alpha 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18794334 1551147 Lama5 laminin, alpha 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20150535 1551147 Lama5 laminin, alpha 5 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16365040 1551147 Lama5 laminin, alpha 5 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:16365040 1551147 Lama5 laminin, alpha 5 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:9852162 1551147 Lama5 laminin, alpha 5 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:16365040 1551147 Lama5 laminin, alpha 5 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:20150535 1551147 Lama5 laminin, alpha 5 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:15936333 1551147 Lama5 laminin, alpha 5 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23847204 1551147 Lama5 laminin, alpha 5 gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:16790509 1551147 Lama5 laminin, alpha 5 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:16790509 1551147 Lama5 laminin, alpha 5 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:20150535 1551147 Lama5 laminin, alpha 5 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:10625553 1551147 Lama5 laminin, alpha 5 gene MP:0003044 impaired basement membrane formation IAGP N RGD:5509061 20141003 MGI PMID:12051813 1551147 Lama5 laminin, alpha 5 gene MP:0003051 curly tail IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:16790509 1551147 Lama5 laminin, alpha 5 gene MP:0003178 left pulmonary isomerism IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16790509 1551147 Lama5 laminin, alpha 5 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12921739 1551147 Lama5 laminin, alpha 5 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:16790509 1551147 Lama5 laminin, alpha 5 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:16365040 1551147 Lama5 laminin, alpha 5 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:12051813 1551147 Lama5 laminin, alpha 5 gene MP:0003675 kidney cyst IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20220428 MGI PMID:28735299 1551147 Lama5 laminin, alpha 5 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:10625553 1551147 Lama5 laminin, alpha 5 gene MP:0003813 abnormal hair follicle dermal papilla morphology IAGP N RGD:5509061 20220428 MGI PMID:28735299 1551147 Lama5 laminin, alpha 5 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15936333 1551147 Lama5 laminin, alpha 5 gene MP:0004157 interrupted aortic arch IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0004158 right aortic arch IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:9852162 1551147 Lama5 laminin, alpha 5 gene MP:0004733 abnormal thoracic cavity morphology IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12921739 1551147 Lama5 laminin, alpha 5 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23847204 1551147 Lama5 laminin, alpha 5 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9852162 1551147 Lama5 laminin, alpha 5 gene MP:0005161 hematuria IAGP N RGD:5509061 20141003 MGI PMID:20150535 1551147 Lama5 laminin, alpha 5 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20150535 1551147 Lama5 laminin, alpha 5 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:20150535 1551147 Lama5 laminin, alpha 5 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10625553 1551147 Lama5 laminin, alpha 5 gene MP:0005327 abnormal mesangial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10625553 1551147 Lama5 laminin, alpha 5 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:20150535 1551147 Lama5 laminin, alpha 5 gene MP:0005502 abnormal renal/urinary system physiology IAGP N RGD:5509061 20141003 MGI PMID:18794334 1551147 Lama5 laminin, alpha 5 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20160929 MGI PMID:27534441 1551147 Lama5 laminin, alpha 5 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16790509 1551147 Lama5 laminin, alpha 5 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20160929 MGI PMID:27534441 1551147 Lama5 laminin, alpha 5 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15936333 1551147 Lama5 laminin, alpha 5 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20220428 MGI PMID:28735299 1551147 Lama5 laminin, alpha 5 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:20150535 1551147 Lama5 laminin, alpha 5 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:23847204 1551147 Lama5 laminin, alpha 5 gene MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23847204 1551147 Lama5 laminin, alpha 5 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:16790509 1551147 Lama5 laminin, alpha 5 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:20150535 1551147 Lama5 laminin, alpha 5 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9852162 1551147 Lama5 laminin, alpha 5 gene MP:0009570 abnormal right lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12051813 1551147 Lama5 laminin, alpha 5 gene MP:0009922 increased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:23847204 1551147 Lama5 laminin, alpha 5 gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:23847204 1551147 Lama5 laminin, alpha 5 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0010460 pulmonary artery hypoplasia IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0010466 vascular ring IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0010487 abnormal right subclavian artery morphology IEA N RGD:5509061 20150827 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0010811 decreased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:15936333 1551147 Lama5 laminin, alpha 5 gene MP:0010817 absent type I pneumocytes IAGP N RGD:5509061 20141003 MGI PMID:15936333 1551147 Lama5 laminin, alpha 5 gene MP:0010821 abnormal visceral pleura morphology IAGP N RGD:5509061 20141003 MGI PMID:12051813 1551147 Lama5 laminin, alpha 5 gene MP:0010898 abnormal pulmonary alveolus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15936333 1551147 Lama5 laminin, alpha 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20150535 1551147 Lama5 laminin, alpha 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15936333 1551147 Lama5 laminin, alpha 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16365040 1551147 Lama5 laminin, alpha 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9852162 1551147 Lama5 laminin, alpha 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551147 Lama5 laminin, alpha 5 gene MP:0011144 thin lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:15936333 1551147 Lama5 laminin, alpha 5 gene MP:0011159 abnormal epidermal-dermal junction morphology IAGP N RGD:5509061 20220428 MGI PMID:28735299 1551147 Lama5 laminin, alpha 5 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:10625553 1551147 Lama5 laminin, alpha 5 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16790509 1551147 Lama5 laminin, alpha 5 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:20150535 1551147 Lama5 laminin, alpha 5 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:20150535 1551147 Lama5 laminin, alpha 5 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16790509 1551147 Lama5 laminin, alpha 5 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:20150535 1551147 Lama5 laminin, alpha 5 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:20150535 1551147 Lama5 laminin, alpha 5 gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10625553 1551147 Lama5 laminin, alpha 5 gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20141003 MGI PMID:9852162 1551147 Lama5 laminin, alpha 5 gene MP:0014084 clubbed small intestinal villi IAGP N RGD:5509061 20220428 MGI PMID:28735299 1551149 Coro7 coronin 7 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20200310 MGI PMID:27143109 1551149 Coro7 coronin 7 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20200310 MGI PMID:27143109 1551149 Coro7 coronin 7 gene MP:0011709 increased fibroblast cell migration IAGP N RGD:5509061 20200310 MGI PMID:27143109 1551149 Coro7 coronin 7 gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20200310 MGI PMID:27143109 1551149 Coro7 coronin 7 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:27143109 1551155 Rtn3 reticulon 3 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20241024 MGI PMID:35596061 1551155 Rtn3 reticulon 3 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20241024 MGI PMID:35596061 1551155 Rtn3 reticulon 3 gene MP:0002959 increased urine microalbumin level IAGP N RGD:5509061 20241024 MGI PMID:35596061 1551155 Rtn3 reticulon 3 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20241024 MGI PMID:25319692 1551155 Rtn3 reticulon 3 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20241024 MGI PMID:35596061 1551155 Rtn3 reticulon 3 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20241024 MGI PMID:35596061 1551155 Rtn3 reticulon 3 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20241024 MGI PMID:35596061 1551155 Rtn3 reticulon 3 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20241024 MGI PMID:35596061 1551155 Rtn3 reticulon 3 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20241024 MGI PMID:35596061 1551155 Rtn3 reticulon 3 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20241024 MGI PMID:35596061 1551155 Rtn3 reticulon 3 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20241024 MGI PMID:35596061 1551155 Rtn3 reticulon 3 gene MP:0011425 abnormal kidney interstitium morphology IAGP N RGD:5509061 20241024 MGI PMID:35596061 1551159 Yeats4 YEATS domain containing 4 gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20200206 MGI PMID:31434684 1551159 Yeats4 YEATS domain containing 4 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20200206 MGI PMID:31434684 1551159 Yeats4 YEATS domain containing 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200206 MGI PMID:31434684 1551159 Yeats4 YEATS domain containing 4 gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20200206 MGI PMID:31434684 1551159 Yeats4 YEATS domain containing 4 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20200206 MGI PMID:31434684 1551159 Yeats4 YEATS domain containing 4 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200206 MGI PMID:31434684 1551159 Yeats4 YEATS domain containing 4 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20200206 MGI PMID:31434684 1551159 Yeats4 YEATS domain containing 4 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20200206 MGI PMID:31434684 1551159 Yeats4 YEATS domain containing 4 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20200206 MGI PMID:31434684 1551159 Yeats4 YEATS domain containing 4 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20200206 MGI PMID:31434684 1551159 Yeats4 YEATS domain containing 4 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20200206 MGI PMID:31434684 1551159 Yeats4 YEATS domain containing 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200206 MGI PMID:31434684 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21505443 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18524855 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:18524855 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0000519 hydronephrosis IEA N RGD:5509061 20111116 MGI 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:21300902 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0001426 polydipsia IEA N RGD:5509061 20111116 MGI 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20160421 MGI 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:21505443 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:18524855 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:21300902 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:21505443 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:21505443 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21505443 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:21505443 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:21300902 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21300902 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:18524855 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0002703 abnormal renal tubule morphology IEA N RGD:5509061 20111116 MGI 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0002988 decreased urine osmolality IEA N RGD:5509061 20111116 MGI 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:18524855 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20141003 MGI PMID:18524855 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21505443 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18524855 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:18524855 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:18524855 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0005633 increased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:18524855 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21300902 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20160421 MGI 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:21505443 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0010858 pulmonary epithelial necrosis IAGP N RGD:5509061 20141003 MGI PMID:21505443 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0010861 increased respiratory mucosa goblet cell number IAGP N RGD:5509061 20141003 MGI PMID:21300902 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21300902 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21505443 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21505443 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:18524855 1551161 Nedd4l neural precursor cell expressed, developmentally down-regulated gene 4-like gene MP:0014206 decreased intestinal epithelial sodium ion transmembrane transport IAGP N RGD:5509061 20160526 MGI PMID:18524855 1551162 Dnah6 dynein, axonemal, heavy chain 6 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200514 MGI 1551162 Dnah6 dynein, axonemal, heavy chain 6 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20201022 MGI 1551162 Dnah6 dynein, axonemal, heavy chain 6 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1551162 Dnah6 dynein, axonemal, heavy chain 6 gene MP:0009709 hydrometra IEA N RGD:5509061 20201022 MGI 1551163 Tas2r105 taste receptor, type 2, member 105 gene MP:0004210 abnormal bitter taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15759003 1551164 Slx1b SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae) gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1551164 Slx1b SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae) gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20200310 MGI PMID:24076219 1551164 Slx1b SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae) gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20200310 MGI PMID:24076219 1551164 Slx1b SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae) gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:26980188 1551164 Slx1b SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae) gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20200310 MGI PMID:24076219 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:30926667 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:30926667 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20200310 MGI PMID:30926667 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:30926667 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:30926667 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0001935 decreased litter size IAGP N RGD:5509061 20210513 MGI PMID:31924127 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210513 MGI PMID:31924127 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210805 MGI PMID:34026442 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20200310 MGI PMID:30926667 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20200310 MGI PMID:30926667 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20200310 MGI PMID:30926667 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20200310 MGI PMID:30926667 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:30926667 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:30926667 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:30926667 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20200310 MGI PMID:30926667 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20200310 MGI PMID:30926667 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20200310 MGI PMID:30926667 1551166 Cnot6l CCR4-NOT transcription complex, subunit 6-like gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:30926667 1551167 Fbxo30 F-box protein 30 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 1551167 Fbxo30 F-box protein 30 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1551167 Fbxo30 F-box protein 30 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1551167 Fbxo30 F-box protein 30 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210520 MGI 1551167 Fbxo30 F-box protein 30 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 1551167 Fbxo30 F-box protein 30 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1551167 Fbxo30 F-box protein 30 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20201022 MGI 1551167 Fbxo30 F-box protein 30 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1551167 Fbxo30 F-box protein 30 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11172041 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:12482969 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:11172041 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:11172041 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:11172041 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11172041 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11172041 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:12482969 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170105 MGI 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12482969 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:11172041 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:11172041 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:11172041 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:12482969 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:17369844 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11172041 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11172041 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12482969 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11172041 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0011187 abnormal parietal endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11172041 1551168 Tsg101 tumor susceptibility gene 101 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:11172041 1551174 Ncstn nicastrin gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21562564 1551174 Ncstn nicastrin gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23359070 1551174 Ncstn nicastrin gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21562564 1551174 Ncstn nicastrin gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12716934 1551174 Ncstn nicastrin gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:12716934 1551174 Ncstn nicastrin gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20160714 MGI PMID:25194568 1551174 Ncstn nicastrin gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:21562564 1551174 Ncstn nicastrin gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21562564 1551174 Ncstn nicastrin gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23359070 1551174 Ncstn nicastrin gene MP:0001212 skin lesions IAGP N RGD:5509061 20161027 MGI PMID:27008863 1551174 Ncstn nicastrin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20161027 MGI PMID:27008863 1551174 Ncstn nicastrin gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20161027 MGI PMID:27008863 1551174 Ncstn nicastrin gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20161027 MGI PMID:27008863 1551174 Ncstn nicastrin gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20161027 MGI PMID:27008863 1551174 Ncstn nicastrin gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19494151 1551174 Ncstn nicastrin gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20161027 MGI PMID:27008863 1551174 Ncstn nicastrin gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:12815056 1551174 Ncstn nicastrin gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16626651 1551174 Ncstn nicastrin gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:12716934 1551174 Ncstn nicastrin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16626651 1551174 Ncstn nicastrin gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21562564 1551174 Ncstn nicastrin gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:23359070 1551174 Ncstn nicastrin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21562564 1551174 Ncstn nicastrin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23359070 1551174 Ncstn nicastrin gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21562564 1551174 Ncstn nicastrin gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12716934 1551174 Ncstn nicastrin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19494151 1551174 Ncstn nicastrin gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:19494151 1551174 Ncstn nicastrin gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:12716934 1551174 Ncstn nicastrin gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19494151 1551174 Ncstn nicastrin gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12716934 1551174 Ncstn nicastrin gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20180125 MGI PMID:16626651 1551174 Ncstn nicastrin gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:19494151 1551174 Ncstn nicastrin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:19494151 1551174 Ncstn nicastrin gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:12716934 1551174 Ncstn nicastrin gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:16626651 1551174 Ncstn nicastrin gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:16626651 1551174 Ncstn nicastrin gene MP:0003587 ureter obstruction IAGP N RGD:5509061 20160714 MGI PMID:25194568 1551174 Ncstn nicastrin gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:16626651 1551174 Ncstn nicastrin gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12716934 1551174 Ncstn nicastrin gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:12716934 1551174 Ncstn nicastrin gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:12716934 1551174 Ncstn nicastrin gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21562564 1551174 Ncstn nicastrin gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21562564 1551174 Ncstn nicastrin gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:19494151 1551174 Ncstn nicastrin gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12716934 1551174 Ncstn nicastrin gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16626651 1551174 Ncstn nicastrin gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:19494151 1551174 Ncstn nicastrin gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16626651 1551174 Ncstn nicastrin gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23359070 1551174 Ncstn nicastrin gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19494151 1551174 Ncstn nicastrin gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:21562564 1551174 Ncstn nicastrin gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20161027 MGI PMID:27008863 1551174 Ncstn nicastrin gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23359070 1551174 Ncstn nicastrin gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19494151 1551174 Ncstn nicastrin gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20160714 MGI PMID:25194568 1551174 Ncstn nicastrin gene MP:0009846 abnormal neural crest morphology IAGP N RGD:5509061 20141003 MGI PMID:16626651 1551174 Ncstn nicastrin gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23359070 1551174 Ncstn nicastrin gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20141003 MGI PMID:23359070 1551174 Ncstn nicastrin gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12815056 1551174 Ncstn nicastrin gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19494151 1551174 Ncstn nicastrin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12716934 1551174 Ncstn nicastrin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16626651 1551174 Ncstn nicastrin gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20161027 MGI PMID:27008863 1551174 Ncstn nicastrin gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16626651 1551174 Ncstn nicastrin gene MP:0013438 dysmyelination IAGP N RGD:5509061 20161027 MGI PMID:27008863 1551174 Ncstn nicastrin gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:19494151 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0001586 abnormal erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20190425 MGI PMID:24510501 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0005563 abnormal hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:18796632 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:20190135 1551178 Gimap5 GTPase, IMAP family member 5 gene MP:0014348 decreased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:20190135 1551179 Des desmin gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:14715896 1551179 Des desmin gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:9281443 1551179 Des desmin gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:10591032 1551179 Des desmin gene MP:0000274 enlarged heart IAGP N RGD:5509061 20171109 MGI PMID:11827695 1551179 Des desmin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10591032 1551179 Des desmin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:14715896 1551179 Des desmin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:8626040 1551179 Des desmin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:8794866 1551179 Des desmin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9281443 1551179 Des desmin gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:9281443 1551179 Des desmin gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:8794866 1551179 Des desmin gene MP:0000751 myopathy IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8794866 1551179 Des desmin gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:8626040 1551179 Des desmin gene MP:0000767 abnormal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8794866 1551179 Des desmin gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:14715896 1551179 Des desmin gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10591032 1551179 Des desmin gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:14715896 1551179 Des desmin gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8626040 1551179 Des desmin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10591032 1551179 Des desmin gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:10591032 1551179 Des desmin gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:8794866 1551179 Des desmin gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:8626040 1551179 Des desmin gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:10591032 1551179 Des desmin gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:10591032 1551179 Des desmin gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:10591032 1551179 Des desmin gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:14715896 1551179 Des desmin gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0002833 increased heart weight IAGP N RGD:5509061 20171109 MGI PMID:11827695 1551179 Des desmin gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:10591032 1551179 Des desmin gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:14715896 1551179 Des desmin gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:8626040 1551179 Des desmin gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:8794866 1551179 Des desmin gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:9281443 1551179 Des desmin gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20171109 MGI PMID:11827695 1551179 Des desmin gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0003057 abnormal epicardium morphology IAGP N RGD:5509061 20141003 MGI PMID:9281443 1551179 Des desmin gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18490514 1551179 Des desmin gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:14715896 1551179 Des desmin gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:8626040 1551179 Des desmin gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9281443 1551179 Des desmin gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20171109 MGI PMID:11827695 1551179 Des desmin gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:8626040 1551179 Des desmin gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20171109 MGI PMID:11827695 1551179 Des desmin gene MP:0003824 decreased left ventricle developed pressure IAGP N RGD:5509061 20171109 MGI PMID:11827695 1551179 Des desmin gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20171109 MGI PMID:11827695 1551179 Des desmin gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9281443 1551179 Des desmin gene MP:0004058 abnormal ventricle papillary muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9281443 1551179 Des desmin gene MP:0004070 abnormal P wave IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:10591032 1551179 Des desmin gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:14715896 1551179 Des desmin gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20171109 MGI PMID:11827695 1551179 Des desmin gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:9281443 1551179 Des desmin gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:9281443 1551179 Des desmin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20171109 MGI PMID:11827695 1551179 Des desmin gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:8794866 1551179 Des desmin gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8626040 1551179 Des desmin gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8794866 1551179 Des desmin gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:8794866 1551179 Des desmin gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20171109 MGI PMID:11827695 1551179 Des desmin gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8626040 1551179 Des desmin gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10591032 1551179 Des desmin gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14715896 1551179 Des desmin gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:14715896 1551179 Des desmin gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:8794866 1551179 Des desmin gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:8626040 1551179 Des desmin gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:10591032 1551179 Des desmin gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:9281443 1551179 Des desmin gene MP:0008543 atrial fibrillation IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:18490514 1551179 Des desmin gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:18490514 1551179 Des desmin gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:18490514 1551179 Des desmin gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:18490514 1551179 Des desmin gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:18490514 1551179 Des desmin gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0009420 skeletal muscle endomysial fibrosis IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0010520 sinoatrial block IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0010553 prolonged HV interval IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20201217 MGI PMID:25179606 1551179 Des desmin gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20160428 MGI PMID:25394388 1551179 Des desmin gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:10591032 1551179 Des desmin gene MP:0014344 abnormal skeletal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:25394388 1551179 Des desmin gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:11827695 1551182 Pmpca peptidase (mitochondrial processing) alpha gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20220811 MGI 1551182 Pmpca peptidase (mitochondrial processing) alpha gene MP:0001284 absent vibrissae IEA N RGD:5509061 20201022 MGI 1551182 Pmpca peptidase (mitochondrial processing) alpha gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1551182 Pmpca peptidase (mitochondrial processing) alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551182 Pmpca peptidase (mitochondrial processing) alpha gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551183 Kif4 kinesin family member 4 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551183 Kif4 kinesin family member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551183 Kif4 kinesin family member 4 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551183 Kif4 kinesin family member 4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1551183 Kif4 kinesin family member 4 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551183 Kif4 kinesin family member 4 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551183 Kif4 kinesin family member 4 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551183 Kif4 kinesin family member 4 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551183 Kif4 kinesin family member 4 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551183 Kif4 kinesin family member 4 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551183 Kif4 kinesin family member 4 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551183 Kif4 kinesin family member 4 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551183 Kif4 kinesin family member 4 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551183 Kif4 kinesin family member 4 gene MP:0012315 impaired learning IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551183 Kif4 kinesin family member 4 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551183 Kif4 kinesin family member 4 gene MP:0021019 increased dendritic spine number IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551183 Kif4 kinesin family member 4 gene MP:0021165 behavioral developmental delay IAGP N RGD:5509061 20240905 MGI PMID:36482480 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0000161 scoliosis IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11829492 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:11829492 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11829492 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:23770692 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23770692 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0009105 penis prolapse IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0009246 pale spleen IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:23770692 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0010894 pulmonary alveolar edema IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11829492 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210218 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20141003 MGI PMID:23770692 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20161027 MGI PMID:23681708 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0020116 increased sphingosine level IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0020582 increased ceramide level IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0030837 abnormal knee joint morphology IAGP N RGD:5509061 20200409 MGI PMID:29908121 1551184 Asah1 N-acylsphingosine amidohydrolase 1 gene MP:0031220 increased circulating CXCL10 level IAGP N RGD:5509061 20210218 MGI PMID:29908121 1551186 Wdr24 WD repeat domain 24 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1551186 Wdr24 WD repeat domain 24 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20230907 MGI PMID:36732624 1551186 Wdr24 WD repeat domain 24 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1551186 Wdr24 WD repeat domain 24 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551186 Wdr24 WD repeat domain 24 gene MP:0013243 abnormal carbohydrate metabolism IAGP N RGD:5509061 20230907 MGI PMID:36732624 1551186 Wdr24 WD repeat domain 24 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1551186 Wdr24 WD repeat domain 24 gene MP:0014257 embryonic lethality prior to tooth bud stage, complete penetrance IAGP N RGD:5509061 20230907 MGI PMID:36732624 1551190 Larp6 La ribonucleoprotein 6, translational regulator gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210128 MGI 1551190 Larp6 La ribonucleoprotein 6, translational regulator gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20200310 MGI 1551190 Larp6 La ribonucleoprotein 6, translational regulator gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20200310 MGI 1551190 Larp6 La ribonucleoprotein 6, translational regulator gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200310 MGI 1551190 Larp6 La ribonucleoprotein 6, translational regulator gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1551192 Id2 inhibitor of DNA binding 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20200310 MGI PMID:15569159 1551192 Id2 inhibitor of DNA binding 2 gene MP:0000526 small inner medullary pyramid IAGP N RGD:5509061 20200310 MGI PMID:15569159 1551192 Id2 inhibitor of DNA binding 2 gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:15601467 1551192 Id2 inhibitor of DNA binding 2 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20200310 MGI PMID:15601467 1551192 Id2 inhibitor of DNA binding 2 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20200310 MGI PMID:14691482 1551192 Id2 inhibitor of DNA binding 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20200310 MGI PMID:19109490 1551192 Id2 inhibitor of DNA binding 2 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20200310 MGI PMID:22522171 1551192 Id2 inhibitor of DNA binding 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:19217292 1551192 Id2 inhibitor of DNA binding 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:15601467 1551192 Id2 inhibitor of DNA binding 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:18562627 1551192 Id2 inhibitor of DNA binding 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:19217292 1551192 Id2 inhibitor of DNA binding 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:10067894 1551192 Id2 inhibitor of DNA binding 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:18562627 1551192 Id2 inhibitor of DNA binding 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20200310 MGI PMID:19217292 1551192 Id2 inhibitor of DNA binding 2 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20200310 MGI PMID:17086188 1551192 Id2 inhibitor of DNA binding 2 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20200310 MGI PMID:10067894 1551192 Id2 inhibitor of DNA binding 2 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20200310 MGI PMID:11060028 1551192 Id2 inhibitor of DNA binding 2 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20200310 MGI PMID:19217292 1551192 Id2 inhibitor of DNA binding 2 gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20200310 MGI PMID:19109490 1551192 Id2 inhibitor of DNA binding 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:22522171 1551192 Id2 inhibitor of DNA binding 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:21587207 1551192 Id2 inhibitor of DNA binding 2 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:17452521 1551192 Id2 inhibitor of DNA binding 2 gene MP:0002219 decreased lymph node number IAGP N RGD:5509061 20200310 MGI PMID:10067894 1551192 Id2 inhibitor of DNA binding 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20200310 MGI PMID:23297132 1551192 Id2 inhibitor of DNA binding 2 gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:14691482 1551192 Id2 inhibitor of DNA binding 2 gene MP:0002379 abnormal oropharyngeal lymphoid tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:12150889 1551192 Id2 inhibitor of DNA binding 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20200310 MGI PMID:23297132 1551192 Id2 inhibitor of DNA binding 2 gene MP:0002450 abnormal lymph organ development IAGP N RGD:5509061 20200310 MGI PMID:14691482 1551192 Id2 inhibitor of DNA binding 2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20200310 MGI PMID:19109490 1551192 Id2 inhibitor of DNA binding 2 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20200310 MGI PMID:10067894 1551192 Id2 inhibitor of DNA binding 2 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20200310 MGI PMID:17452521 1551192 Id2 inhibitor of DNA binding 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:22522171 1551192 Id2 inhibitor of DNA binding 2 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20200310 MGI PMID:19109490 1551192 Id2 inhibitor of DNA binding 2 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20200310 MGI PMID:19109490 1551192 Id2 inhibitor of DNA binding 2 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20200310 MGI PMID:22522171 1551192 Id2 inhibitor of DNA binding 2 gene MP:0003622 ischuria IAGP N RGD:5509061 20200310 MGI PMID:15569159 1551192 Id2 inhibitor of DNA binding 2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20200310 MGI PMID:19217292 1551192 Id2 inhibitor of DNA binding 2 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20200310 MGI PMID:19109490 1551192 Id2 inhibitor of DNA binding 2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200310 MGI PMID:19109490 1551192 Id2 inhibitor of DNA binding 2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200310 MGI PMID:22522171 1551192 Id2 inhibitor of DNA binding 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:17452521 1551192 Id2 inhibitor of DNA binding 2 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:18562627 1551192 Id2 inhibitor of DNA binding 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210520 MGI 1551192 Id2 inhibitor of DNA binding 2 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210520 MGI 1551192 Id2 inhibitor of DNA binding 2 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20200310 MGI PMID:11060028 1551192 Id2 inhibitor of DNA binding 2 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:17086188 1551192 Id2 inhibitor of DNA binding 2 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:17452521 1551192 Id2 inhibitor of DNA binding 2 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20200310 MGI PMID:17452521 1551192 Id2 inhibitor of DNA binding 2 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20200310 MGI PMID:10067894 1551192 Id2 inhibitor of DNA binding 2 gene MP:0008046 absent NK cells IAGP N RGD:5509061 20200310 MGI PMID:17086188 1551192 Id2 inhibitor of DNA binding 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:17086188 1551192 Id2 inhibitor of DNA binding 2 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20200310 MGI PMID:17452521 1551192 Id2 inhibitor of DNA binding 2 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20200310 MGI PMID:22522171 1551192 Id2 inhibitor of DNA binding 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:19217292 1551192 Id2 inhibitor of DNA binding 2 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:18562627 1551192 Id2 inhibitor of DNA binding 2 gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:18562627 1551192 Id2 inhibitor of DNA binding 2 gene MP:0009485 distended ileum IAGP N RGD:5509061 20200310 MGI PMID:10067894 1551192 Id2 inhibitor of DNA binding 2 gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:17452521 1551192 Id2 inhibitor of DNA binding 2 gene MP:0009628 absent brachial lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:17452521 1551192 Id2 inhibitor of DNA binding 2 gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:17452521 1551192 Id2 inhibitor of DNA binding 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20200310 MGI PMID:22522171 1551192 Id2 inhibitor of DNA binding 2 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:15601467 1551192 Id2 inhibitor of DNA binding 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18562627 1551192 Id2 inhibitor of DNA binding 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10067894 1551192 Id2 inhibitor of DNA binding 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22522171 1551192 Id2 inhibitor of DNA binding 2 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20200310 MGI PMID:22522171 1551192 Id2 inhibitor of DNA binding 2 gene MP:0011487 abnormal ureteropelvic junction morphology IAGP N RGD:5509061 20200310 MGI PMID:15569159 1551192 Id2 inhibitor of DNA binding 2 gene MP:0011490 ureteropelvic junction stenosis IAGP N RGD:5509061 20200310 MGI PMID:15569159 1551192 Id2 inhibitor of DNA binding 2 gene MP:0011503 distended jejunum IAGP N RGD:5509061 20200310 MGI PMID:10067894 1551192 Id2 inhibitor of DNA binding 2 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20200310 MGI PMID:19217292 1551192 Id2 inhibitor of DNA binding 2 gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20200310 MGI PMID:19217292 1551193 Atp13a5 ATPase type 13A5 gene MP:0002635 reduced sensorimotor gating IEA N RGD:5509061 20200310 MGI 1551193 Atp13a5 ATPase type 13A5 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20200310 MGI 1551194 Steap3 STEAP family member 3 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:16227996 1551194 Steap3 STEAP family member 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20200310 MGI PMID:18955558 1551194 Steap3 STEAP family member 3 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:18955558 1551194 Steap3 STEAP family member 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1551194 Steap3 STEAP family member 3 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0002424 abnormal reticulocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:16227996 1551194 Steap3 STEAP family member 3 gene MP:0002424 abnormal reticulocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:16227996 1551194 Steap3 STEAP family member 3 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20200310 MGI PMID:16227996 1551194 Steap3 STEAP family member 3 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20200310 MGI PMID:16227996 1551194 Steap3 STEAP family member 3 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20200310 MGI PMID:18955558 1551194 Steap3 STEAP family member 3 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20200310 MGI PMID:16227996 1551194 Steap3 STEAP family member 3 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20200310 MGI PMID:18955558 1551194 Steap3 STEAP family member 3 gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:16227996 1551194 Steap3 STEAP family member 3 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:18955558 1551194 Steap3 STEAP family member 3 gene MP:0003066 increased liver copper level IAGP N RGD:5509061 20200310 MGI PMID:18955558 1551194 Steap3 STEAP family member 3 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:16227996 1551194 Steap3 STEAP family member 3 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:18955558 1551194 Steap3 STEAP family member 3 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20200310 MGI PMID:18955558 1551194 Steap3 STEAP family member 3 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20201022 MGI 1551194 Steap3 STEAP family member 3 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20200310 MGI PMID:16227996 1551194 Steap3 STEAP family member 3 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20200310 MGI PMID:16227996 1551194 Steap3 STEAP family member 3 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20200310 MGI PMID:16227996 1551194 Steap3 STEAP family member 3 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20200310 MGI PMID:18955558 1551194 Steap3 STEAP family member 3 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20200310 MGI PMID:16227996 1551194 Steap3 STEAP family member 3 gene MP:0006349 decreased circulating copper level IAGP N RGD:5509061 20200310 MGI PMID:18955558 1551194 Steap3 STEAP family member 3 gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20200310 MGI PMID:18955558 1551194 Steap3 STEAP family member 3 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20200310 MGI PMID:16227996 1551194 Steap3 STEAP family member 3 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20200310 MGI PMID:18955558 1551194 Steap3 STEAP family member 3 gene MP:0008996 abnormal blood osmolality IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0009341 decreased splenocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:18617898 1551194 Steap3 STEAP family member 3 gene MP:0010175 leptocytosis IAGP N RGD:5509061 20200310 MGI PMID:18955558 1551195 Eif3k eukaryotic translation initiation factor 3, subunit K gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230119 MGI 1551195 Eif3k eukaryotic translation initiation factor 3, subunit K gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20230119 MGI 1551195 Eif3k eukaryotic translation initiation factor 3, subunit K gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20230119 MGI 1551195 Eif3k eukaryotic translation initiation factor 3, subunit K gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1551197 Unk unkempt family zinc finger gene MP:0000520 absent kidney IEA N RGD:5509061 20200310 MGI 1551197 Unk unkempt family zinc finger gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20200310 MGI 1551197 Unk unkempt family zinc finger gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1551197 Unk unkempt family zinc finger gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220908 MGI PMID:34381067 1551197 Unk unkempt family zinc finger gene MP:0002947 increased hemangioma incidence IEA N RGD:5509061 20210930 MGI 1551197 Unk unkempt family zinc finger gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20210520 MGI 1551197 Unk unkempt family zinc finger gene MP:0003722 absent ureter IEA N RGD:5509061 20200310 MGI 1551197 Unk unkempt family zinc finger gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 1551197 Unk unkempt family zinc finger gene MP:0009532 decreased parotid gland size IEA N RGD:5509061 20200310 MGI 1551197 Unk unkempt family zinc finger gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1551197 Unk unkempt family zinc finger gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20200310 MGI 1551197 Unk unkempt family zinc finger gene MP:0010977 fused right lung lobes IEA N RGD:5509061 20200310 MGI 1551197 Unk unkempt family zinc finger gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551197 Unk unkempt family zinc finger gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20200310 MGI 1551197 Unk unkempt family zinc finger gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20200310 MGI 1551197 Unk unkempt family zinc finger gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20200310 MGI 1551197 Unk unkempt family zinc finger gene MP:0014114 abnormal cognition IAGP N RGD:5509061 20220908 MGI PMID:34381067 1551198 Unc13b unc-13 homolog B gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:12070347 1551198 Unc13b unc-13 homolog B gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20181227 MGI 1551198 Unc13b unc-13 homolog B gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 1551198 Unc13b unc-13 homolog B gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:17267576 1551198 Unc13b unc-13 homolog B gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17267576 1551198 Unc13b unc-13 homolog B gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21040848 1551198 Unc13b unc-13 homolog B gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12070347 1551198 Unc13b unc-13 homolog B gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22674279 1551198 Unc13b unc-13 homolog B gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22674279 1551198 Unc13b unc-13 homolog B gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17267576 1551198 Unc13b unc-13 homolog B gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17267576 1551198 Unc13b unc-13 homolog B gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:12070347 1551198 Unc13b unc-13 homolog B gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:17267576 1551198 Unc13b unc-13 homolog B gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21040848 1551198 Unc13b unc-13 homolog B gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22674279 1551198 Unc13b unc-13 homolog B gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:12070347 1551198 Unc13b unc-13 homolog B gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:22674279 1551198 Unc13b unc-13 homolog B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12070347 1551198 Unc13b unc-13 homolog B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20160602 MGI PMID:24789067 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0000088 short mandible IEA N RGD:5509061 20111116 MGI 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18538759 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210128 MGI 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:20197625 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:17943079 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:20197625 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:20197625 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20160602 MGI PMID:24789067 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20197625 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0003755 abnormal palate morphology IEA N RGD:5509061 20111116 MGI 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0003756 abnormal hard palate morphology IEA N RGD:5509061 20111215 MGI 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0003932 abnormal molar crown morphology IAGP N RGD:5509061 20141003 MGI PMID:16179481 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20141003 MGI PMID:16341262 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20160602 MGI PMID:24789067 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20160602 MGI PMID:24789067 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20160602 MGI PMID:24789067 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:20197625 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:20197625 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:20197625 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20160602 MGI PMID:24789067 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20197625 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0006369 supernumerary incisors IEA N RGD:5509061 20111116 MGI 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20160602 MGI PMID:24789067 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0008525 decreased cranium height IEA N RGD:5509061 20111116 MGI 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0008526 decreased cranium width IEA N RGD:5509061 20111116 MGI 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16341262 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20141003 MGI PMID:19782673 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16341262 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20160602 MGI PMID:24789067 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0010773 supernumerary molars IAGP N RGD:5509061 20171228 MGI PMID:16179481 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0010864 abnormal enamel knot morphology IAGP N RGD:5509061 20171228 MGI PMID:16179481 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20160602 MGI PMID:24789067 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18538759 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20160602 MGI PMID:24789067 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:20197625 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0011372 decreased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16341262 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:20197625 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20160602 MGI PMID:24789067 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0030438 increased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:24789067 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20171228 MGI PMID:16179481 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0030473 fused molars IAGP N RGD:5509061 20171228 MGI PMID:16179481 1551201 Sostdc1 sclerostin domain containing 1 gene MP:0030473 fused molars IAGP N RGD:5509061 20171228 MGI PMID:16341262 1551202 Noc4l NOC4 like gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1551202 Noc4l NOC4 like gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1551202 Noc4l NOC4 like gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28012024 1551202 Noc4l NOC4 like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1551202 Noc4l NOC4 like gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1551202 Noc4l NOC4 like gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:28012024 1551203 Spam1 sperm adhesion molecule 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20200310 MGI PMID:12065596 1551203 Spam1 sperm adhesion molecule 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20200310 MGI PMID:19605784 1551203 Spam1 sperm adhesion molecule 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20200310 MGI PMID:19605784 1551204 Degs2 delta 4-desaturase, sphingolipid 2 gene MP:0020583 decreased ceramide level IAGP N RGD:5509061 20231109 MGI PMID:36907437 1551206 Olfml2b olfactomedin-like 2B gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 1551210 Pafah2 platelet-activating factor acetylhydrolase 2 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:18024956 1551210 Pafah2 platelet-activating factor acetylhydrolase 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18024956 1551210 Pafah2 platelet-activating factor acetylhydrolase 2 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:18024956 1551212 Dnajc18 DnaJ heat shock protein family (Hsp40) member C18 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551215 Cdc37l1 cell division cycle 37-like 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20201022 MGI 1551215 Cdc37l1 cell division cycle 37-like 1 gene MP:0001304 cataract IEA N RGD:5509061 20210826 MGI 1551215 Cdc37l1 cell division cycle 37-like 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20200310 MGI 1551215 Cdc37l1 cell division cycle 37-like 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1551220 Lmbr1l limb region 1 like gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20200310 MGI 1551220 Lmbr1l limb region 1 like gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0002491 decreased IgD level IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1551220 Lmbr1l limb region 1 like gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0011181 increased hematopoietic cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0012762 abnormal alpha-beta T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0013893 decreased common lymphocyte progenitor cell number IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551220 Lmbr1l limb region 1 like gene MP:0020154 impaired humoral immune response IAGP N RGD:5509061 20200310 MGI PMID:31073040 1551221 Babam2 BRISC and BRCA1 A complex member 2 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20141003 MGI 1551221 Babam2 BRISC and BRCA1 A complex member 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20141003 MGI 1551221 Babam2 BRISC and BRCA1 A complex member 2 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1551221 Babam2 BRISC and BRCA1 A complex member 2 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20170615 MGI PMID:27001068 1551221 Babam2 BRISC and BRCA1 A complex member 2 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20170615 MGI PMID:27001068 1551221 Babam2 BRISC and BRCA1 A complex member 2 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20170615 MGI PMID:27001068 1551221 Babam2 BRISC and BRCA1 A complex member 2 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20170615 MGI PMID:27001068 1551226 Sec23ip Sec23 interacting protein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:21640725 1551226 Sec23ip Sec23 interacting protein gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20230309 MGI PMID:21640725 1551226 Sec23ip Sec23 interacting protein gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21640725 1551226 Sec23ip Sec23 interacting protein gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:21640725 1551226 Sec23ip Sec23 interacting protein gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20230309 MGI PMID:21640725 1551226 Sec23ip Sec23 interacting protein gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20230309 MGI PMID:21640725 1551226 Sec23ip Sec23 interacting protein gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20230309 MGI PMID:21640725 1551226 Sec23ip Sec23 interacting protein gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20230309 MGI PMID:21640725 1551227 Cct3 chaperonin containing TCP1 subunit 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210520 MGI 1551227 Cct3 chaperonin containing TCP1 subunit 3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1551227 Cct3 chaperonin containing TCP1 subunit 3 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20220519 MGI 1551227 Cct3 chaperonin containing TCP1 subunit 3 gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20240523 MGI 1551227 Cct3 chaperonin containing TCP1 subunit 3 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1551227 Cct3 chaperonin containing TCP1 subunit 3 gene MP:0006206 embryonic lethality between somite formation and embryo turning IEA N RGD:5509061 20141003 MGI 1551227 Cct3 chaperonin containing TCP1 subunit 3 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20230601 MGI 1551227 Cct3 chaperonin containing TCP1 subunit 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1551227 Cct3 chaperonin containing TCP1 subunit 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1551231 Tmem64 transmembrane protein 64 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551231 Tmem64 transmembrane protein 64 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551231 Tmem64 transmembrane protein 64 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551231 Tmem64 transmembrane protein 64 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551231 Tmem64 transmembrane protein 64 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551231 Tmem64 transmembrane protein 64 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551231 Tmem64 transmembrane protein 64 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551231 Tmem64 transmembrane protein 64 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551231 Tmem64 transmembrane protein 64 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551231 Tmem64 transmembrane protein 64 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551231 Tmem64 transmembrane protein 64 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551231 Tmem64 transmembrane protein 64 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551231 Tmem64 transmembrane protein 64 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551231 Tmem64 transmembrane protein 64 gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551231 Tmem64 transmembrane protein 64 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551231 Tmem64 transmembrane protein 64 gene MP:0030984 increased circulating osteocalcin level IAGP N RGD:5509061 20200310 MGI PMID:23395171 1551233 Marchf8 membrane associated ring-CH-type finger 8 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200514 MGI 1551233 Marchf8 membrane associated ring-CH-type finger 8 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200514 MGI 1551233 Marchf8 membrane associated ring-CH-type finger 8 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1551233 Marchf8 membrane associated ring-CH-type finger 8 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20240523 MGI 1551233 Marchf8 membrane associated ring-CH-type finger 8 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1551233 Marchf8 membrane associated ring-CH-type finger 8 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 1551233 Marchf8 membrane associated ring-CH-type finger 8 gene MP:0010935 increased airway resistance IEA N RGD:5509061 20220519 MGI 1551235 Bcap29 B cell receptor associated protein 29 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220519 MGI 1551235 Bcap29 B cell receptor associated protein 29 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1551235 Bcap29 B cell receptor associated protein 29 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000162 lordosis IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20200310 MGI PMID:22144916 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20200310 MGI PMID:22144916 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20200310 MGI PMID:24721909 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20200310 MGI PMID:25340873 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20200310 MGI PMID:25340873 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0000961 abnormal dorsal root ganglion morphology IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20200310 MGI PMID:24721909 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:22144916 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0001304 cataract IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0001349 excessive tearing IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20200310 MGI PMID:25340873 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20200310 MGI PMID:25340873 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:22144916 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0002368 abnormal thymus capsule morphology IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0004160 retroesophageal right subclavian artery IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0004463 basisphenoid bone foramen IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0004666 absent stapedial artery IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0008805 decreased circulating amylase level IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20200310 MGI PMID:22144916 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20200310 MGI PMID:25340873 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0008861 abnormal hair shedding IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0008861 abnormal hair shedding IAGP N RGD:5509061 20200310 MGI PMID:25340873 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0008923 thoracoschisis IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0009770 abnormal optic chiasm morphology IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25340873 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0011655 abnormal systemic artery morphology IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20200310 MGI PMID:24652767 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013826 absent hypoglossal canal IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013842 ductus venosus stenosis IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013875 increased trigeminal neuroma incidence IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013928 thin motoric part of trigeminal nerve IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013948 intraembryonal intestine elongation IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013992 persistent dorsal ophthalmic artery IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0013995 abnormal external carotid artery origin IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20200310 MGI 1551238 Nsun2 NOL1/NOP2/Sun domain family member 2 gene MP:0020500 persistent trigeminal artery IEA N RGD:5509061 20200310 MGI 1551239 Arfip2 ADP-ribosylation factor interacting protein 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20240328 MGI PMID:38247505 1551239 Arfip2 ADP-ribosylation factor interacting protein 2 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20240328 MGI PMID:38247505 1551239 Arfip2 ADP-ribosylation factor interacting protein 2 gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20240328 MGI PMID:38247505 1551239 Arfip2 ADP-ribosylation factor interacting protein 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20240328 MGI PMID:38247505 1551239 Arfip2 ADP-ribosylation factor interacting protein 2 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20240328 MGI PMID:38247505 1551241 St3gal1 ST3 beta-galactoside alpha-2,3-sialyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:10755614 1551241 St3gal1 ST3 beta-galactoside alpha-2,3-sialyltransferase 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:12077344 1551242 Tspan3 tetraspanin 3 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20160623 MGI PMID:26212080 1551242 Tspan3 tetraspanin 3 gene MP:0011995 decreased leukemia incidence IAGP N RGD:5509061 20160623 MGI PMID:26212080 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20200310 MGI PMID:25557619 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20200310 MGI PMID:25557619 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25557619 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0020078 decreased brain tyrosine 3-monooxygenase activity IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0020875 decreased nervous system dopamine level IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551245 Gch1 GTP cyclohydrolase 1 gene MP:0030697 increased phenylalanine level IAGP N RGD:5509061 20201210 MGI PMID:30742839 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0002899 fatigue IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0011134 decreased lung endothelial cell migration IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551247 Aggf1 angiogenic factor with G patch and FHA domains 1 gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20200310 MGI PMID:27522498 1551248 Lrrc38 leucine rich repeat containing 38 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20231207 MGI 1551248 Lrrc38 leucine rich repeat containing 38 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1551248 Lrrc38 leucine rich repeat containing 38 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1551249 Vsx2 visual system homeobox 2 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20150611 MGI PMID:640793 1551249 Vsx2 visual system homeobox 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:13994395 1551249 Vsx2 visual system homeobox 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:827941 1551249 Vsx2 visual system homeobox 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:13994395 1551249 Vsx2 visual system homeobox 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15223342 1551249 Vsx2 visual system homeobox 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:23028343 1551249 Vsx2 visual system homeobox 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:827941 1551249 Vsx2 visual system homeobox 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:13994395 1551249 Vsx2 visual system homeobox 2 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:23028343 1551249 Vsx2 visual system homeobox 2 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:827941 1551249 Vsx2 visual system homeobox 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23028343 1551249 Vsx2 visual system homeobox 2 gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:15223342 1551249 Vsx2 visual system homeobox 2 gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:827941 1551249 Vsx2 visual system homeobox 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:13994395 1551249 Vsx2 visual system homeobox 2 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:13994395 1551249 Vsx2 visual system homeobox 2 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:827941 1551249 Vsx2 visual system homeobox 2 gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 1551249 Vsx2 visual system homeobox 2 gene MP:0001926 female infertility IEA N RGD:5509061 20111116 MGI 1551249 Vsx2 visual system homeobox 2 gene MP:0001929 abnormal gametogenesis IEA N RGD:5509061 20111116 MGI 1551249 Vsx2 visual system homeobox 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:23028343 1551249 Vsx2 visual system homeobox 2 gene MP:0002697 abnormal eye size IAGP N RGD:5509061 20141003 MGI PMID:16783634 1551249 Vsx2 visual system homeobox 2 gene MP:0002697 abnormal eye size IAGP N RGD:5509061 20141003 MGI PMID:23028343 1551249 Vsx2 visual system homeobox 2 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:23028343 1551249 Vsx2 visual system homeobox 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18940589 1551249 Vsx2 visual system homeobox 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:24267650 1551249 Vsx2 visual system homeobox 2 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20150611 MGI PMID:1181211 1551249 Vsx2 visual system homeobox 2 gene MP:0004100 abnormal spinal cord interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18940589 1551249 Vsx2 visual system homeobox 2 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:13994395 1551249 Vsx2 visual system homeobox 2 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:827941 1551249 Vsx2 visual system homeobox 2 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20150611 MGI PMID:640793 1551249 Vsx2 visual system homeobox 2 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:827941 1551249 Vsx2 visual system homeobox 2 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:23028343 1551249 Vsx2 visual system homeobox 2 gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:827941 1551249 Vsx2 visual system homeobox 2 gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20141003 MGI PMID:827941 1551249 Vsx2 visual system homeobox 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23028343 1551249 Vsx2 visual system homeobox 2 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:827941 1551249 Vsx2 visual system homeobox 2 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15223342 1551249 Vsx2 visual system homeobox 2 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:827941 1551249 Vsx2 visual system homeobox 2 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20150611 MGI PMID:640793 1551249 Vsx2 visual system homeobox 2 gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20141003 MGI PMID:15223342 1551249 Vsx2 visual system homeobox 2 gene MP:0008503 abnormal spinal cord grey matter morphology IAGP N RGD:5509061 20141003 MGI PMID:24267650 1551249 Vsx2 visual system homeobox 2 gene MP:0009771 absent optic chiasm IAGP N RGD:5509061 20150611 MGI PMID:13994395 1551249 Vsx2 visual system homeobox 2 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:23028343 1551249 Vsx2 visual system homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18940589 1551249 Vsx2 visual system homeobox 2 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:23028343 1551249 Vsx2 visual system homeobox 2 gene MP:0012534 abnormal optic fissure morphology IAGP N RGD:5509061 20141003 MGI PMID:827941 1551249 Vsx2 visual system homeobox 2 gene MP:0012537 abnormal hyaloid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:827941 1551249 Vsx2 visual system homeobox 2 gene MP:0013447 Harderian gland hypertrophy IAGP N RGD:5509061 20150205 MGI PMID:13994395 1551249 Vsx2 visual system homeobox 2 gene MP:0013454 lacrimal gland hypertrophy IAGP N RGD:5509061 20150205 MGI PMID:13994395 1551249 Vsx2 visual system homeobox 2 gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:18940589 1551250 Trpc7 transient receptor potential cation channel, subfamily C, member 7 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:21261756 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:14679186 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0001263 weight loss IEA N RGD:5509061 20141003 MGI 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:14679186 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0001858 intestinal inflammation IEA N RGD:5509061 20141003 MGI 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:14679186 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:14679186 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:14679186 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14679186 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:14679186 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0005036 diarrhea IEA N RGD:5509061 20141003 MGI 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:14679186 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20141003 MGI 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:14679186 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:14679186 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0010111 abnormal renal calcium reabsorption IAGP N RGD:5509061 20141003 MGI PMID:14679186 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:14679186 1551251 Trpv5 transient receptor potential cation channel, subfamily V, member 5 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:23383183 1551253 Cited4 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0000263 absent organized vascular network IAGP N RGD:5509061 20171116 MGI PMID:25328912 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20231116 MGI PMID:33773996 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20171116 MGI PMID:25328912 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20231116 MGI PMID:33773996 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20231116 MGI PMID:33773996 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:33773996 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20231116 MGI PMID:33773996 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20171116 MGI PMID:25328912 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20171116 MGI PMID:25328912 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20231116 MGI PMID:33773996 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20171116 MGI PMID:25328912 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20231116 MGI PMID:33773996 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20231116 MGI PMID:33773996 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0010502 ventricle myocardium hypoplasia IAGP N RGD:5509061 20231116 MGI PMID:33773996 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20231116 MGI PMID:33773996 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20231116 MGI PMID:33773996 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20171116 MGI PMID:25328912 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20231116 MGI PMID:33773996 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0013258 abnormal extracellular matrix morphology IAGP N RGD:5509061 20231116 MGI PMID:33773996 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20171116 MGI PMID:25328912 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20191128 MGI PMID:25328912 1551256 Creld1 cysteine-rich with EGF-like domains 1 gene MP:0031128 cardiovascular shunt IAGP N RGD:5509061 20231116 MGI PMID:33773996 1551257 Nrp2 neuropilin 2 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:18657176 1551257 Nrp2 neuropilin 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:11891274 1551257 Nrp2 neuropilin 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20065093 1551257 Nrp2 neuropilin 2 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:22726444 1551257 Nrp2 neuropilin 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17942483 1551257 Nrp2 neuropilin 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12019322 1551257 Nrp2 neuropilin 2 gene MP:0001061 abnormal oculomotor nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10707971 1551257 Nrp2 neuropilin 2 gene MP:0001064 absent trochlear nerve IAGP N RGD:5509061 20141003 MGI PMID:10707971 1551257 Nrp2 neuropilin 2 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10707971 1551257 Nrp2 neuropilin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17362911 1551257 Nrp2 neuropilin 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11891274 1551257 Nrp2 neuropilin 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12019322 1551257 Nrp2 neuropilin 2 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:20065093 1551257 Nrp2 neuropilin 2 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20170525 MGI PMID:26319580 1551257 Nrp2 neuropilin 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:12019322 1551257 Nrp2 neuropilin 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11891274 1551257 Nrp2 neuropilin 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:12019322 1551257 Nrp2 neuropilin 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:18657176 1551257 Nrp2 neuropilin 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:17362911 1551257 Nrp2 neuropilin 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:12852851 1551257 Nrp2 neuropilin 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15550623 1551257 Nrp2 neuropilin 2 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10707971 1551257 Nrp2 neuropilin 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:18657176 1551257 Nrp2 neuropilin 2 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:12019322 1551257 Nrp2 neuropilin 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11891274 1551257 Nrp2 neuropilin 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18657176 1551257 Nrp2 neuropilin 2 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:18434520 1551257 Nrp2 neuropilin 2 gene MP:0004082 abnormal habenula morphology IAGP N RGD:5509061 20141003 MGI PMID:10707971 1551257 Nrp2 neuropilin 2 gene MP:0004106 lymphatic vessel hyperplasia IAGP N RGD:5509061 20170525 MGI PMID:26319580 1551257 Nrp2 neuropilin 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:11891274 1551257 Nrp2 neuropilin 2 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:18657176 1551257 Nrp2 neuropilin 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:18434520 1551257 Nrp2 neuropilin 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18657176 1551257 Nrp2 neuropilin 2 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:10707971 1551257 Nrp2 neuropilin 2 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:12852851 1551257 Nrp2 neuropilin 2 gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20065093 1551257 Nrp2 neuropilin 2 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:18657176 1551257 Nrp2 neuropilin 2 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:10707971 1551257 Nrp2 neuropilin 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18657176 1551257 Nrp2 neuropilin 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:18657176 1551257 Nrp2 neuropilin 2 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18657176 1551257 Nrp2 neuropilin 2 gene MP:0010197 abnormal lymphatic vessel endothelial cell morphology IAGP N RGD:5509061 20170525 MGI PMID:26319580 1551257 Nrp2 neuropilin 2 gene MP:0010368 abnormal lymphatic system physiology IAGP N RGD:5509061 20170525 MGI PMID:26319580 1551257 Nrp2 neuropilin 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12852851 1551257 Nrp2 neuropilin 2 gene MP:0010860 abnormal anterior commissure pars posterior morphology IAGP N RGD:5509061 20141003 MGI PMID:10707971 1551257 Nrp2 neuropilin 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18657176 1551257 Nrp2 neuropilin 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17362911 1551257 Nrp2 neuropilin 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11891274 1551257 Nrp2 neuropilin 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12019322 1551257 Nrp2 neuropilin 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20065093 1551257 Nrp2 neuropilin 2 gene MP:0011678 abnormal vomeronasal sensory neuron physiology IAGP N RGD:5509061 20150319 MGI PMID:12019322 1551257 Nrp2 neuropilin 2 gene MP:0011679 abnormal vomeronasal sensory neuron morphology IAGP N RGD:5509061 20150319 MGI PMID:12019322 1551257 Nrp2 neuropilin 2 gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12019322 1551259 Zfp687 zinc finger protein 687 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1551261 Morf4l2 mortality factor 4 like 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15923606 1551261 Morf4l2 mortality factor 4 like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15923606 1551261 Morf4l2 mortality factor 4 like 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15923606 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:19059914 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20200310 MGI PMID:21308779 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20200310 MGI PMID:21308779 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20200310 MGI PMID:19059914 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20200310 MGI PMID:18552211 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:18552211 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20200310 MGI PMID:16651614 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20200310 MGI PMID:10411532 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:19734231 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:19734231 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20200310 MGI PMID:19059914 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20200310 MGI PMID:18552211 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0001606 impaired hematopoiesis IEA N RGD:5509061 20200310 MGI 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20200310 MGI PMID:19923276 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19059914 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20200310 MGI PMID:10894167 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20200310 MGI PMID:18354038 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20200310 MGI PMID:18552211 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:19339614 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:21709234 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:24048899 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:8456301 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20211216 MGI PMID:31964735 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:16123129 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:8871615 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0003332 liver abscess IAGP N RGD:5509061 20200310 MGI PMID:21709234 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20200310 MGI PMID:19339614 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20200310 MGI PMID:9164973 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0003884 decreased macrophage cell number IEA N RGD:5509061 20200310 MGI 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:8871615 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20200310 MGI PMID:9169506 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20200310 MGI PMID:10329607 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20200310 MGI PMID:10411532 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0004795 decreased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200310 MGI PMID:8871615 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0004821 increased susceptibility to experimental autoimmune uveoretinitis IAGP N RGD:5509061 20200310 MGI PMID:15902435 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0004824 decreased susceptibility to experimental autoimmune myasthenia gravis IAGP N RGD:5509061 20200310 MGI PMID:10201893 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20200310 MGI PMID:19059914 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20200310 MGI PMID:21308779 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20200310 MGI PMID:21308779 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0005014 increased B cell number IEA N RGD:5509061 20200310 MGI 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:18552211 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20200310 MGI PMID:23999498 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20200310 MGI PMID:9687534 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20200310 MGI PMID:10329607 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:8456301 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:9169506 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20200310 MGI PMID:9169506 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0005672 increased susceptibility to graft versus host disease IAGP N RGD:5509061 20200310 MGI PMID:18552211 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008054 abnormal uterine NK cell morphology IAGP N RGD:5509061 20200310 MGI PMID:10411532 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18552211 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18552211 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20200310 MGI PMID:19059914 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20200310 MGI PMID:21308779 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:8456301 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:8871615 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:9164973 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20200310 MGI PMID:8456301 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:15265950 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20200310 MGI PMID:8163930 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20200310 MGI PMID:8871615 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008561 decreased tumor necrosis factor secretion IEA N RGD:5509061 20200310 MGI 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:15902435 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:18552211 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:8871615 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:24048899 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20211216 MGI PMID:31964735 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20200310 MGI PMID:19734231 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20200310 MGI PMID:21709234 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008618 decreased circulating interleukin-12 level IAGP N RGD:5509061 20200310 MGI PMID:19734231 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20211216 MGI PMID:31964735 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20200310 MGI PMID:24048899 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20200310 MGI PMID:15902435 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20200310 MGI PMID:19734231 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20200310 MGI PMID:8163930 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:16651614 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0009099 abnormal uterine NK cell physiology IAGP N RGD:5509061 20200310 MGI PMID:10411532 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:15902435 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20200310 MGI PMID:21308779 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0009394 increased uterine NK cell number IAGP N RGD:5509061 20200310 MGI PMID:10411532 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:18552211 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:8871615 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:21709234 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:24048899 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20211216 MGI PMID:31964735 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0010138 arteritis IAGP N RGD:5509061 20200310 MGI PMID:9687534 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0010139 aortitis IAGP N RGD:5509061 20200310 MGI PMID:9687534 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20200310 MGI PMID:10894167 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20200310 MGI PMID:19734231 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0010280 increased skeletal tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19059914 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0010331 abnormal apolipoprotein level IAGP N RGD:5509061 20200310 MGI PMID:9169506 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:21308779 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20200310 MGI PMID:21308779 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20200310 MGI PMID:21308779 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20200310 MGI PMID:21308779 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:21308779 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:8456301 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:11390995 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0020928 increased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16123129 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0020940 increased susceptibility to Togaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:11390995 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0030483 decreased osteocyte number IAGP N RGD:5509061 20200310 MGI PMID:21308779 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0030985 decreased circulating osteocalcin level IAGP N RGD:5509061 20200310 MGI PMID:21308779 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:8456301 1551263 Ifngr1 interferon gamma receptor 1 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:9687534 1551267 Intu inturned planar cell polarity protein gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0000562 polydactyly IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0000831 diencephalon hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0000914 exencephaly IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0000927 small floor plate IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20160929 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0004203 abnormal cranial flexure morphology IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0004574 broad limb buds IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20160929 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20160929 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0011065 abnormal kidney epithelial cell primary cilium morphology IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0011998 decreased embryonic cilium length IAGP N RGD:5509061 20160929 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0011998 decreased embryonic cilium length IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0013197 decreased embryonic cilium number IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20160929 MGI PMID:20067783 1551267 Intu inturned planar cell polarity protein gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0013213 abnormal embryonic neuroepithelium primary cilium morphology IAGP N RGD:5509061 20160929 MGI PMID:25774014 1551267 Intu inturned planar cell polarity protein gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:20067783 1551268 Rln3 relaxin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19416195 1551268 Rln3 relaxin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19416196 1551268 Rln3 relaxin 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19416196 1551268 Rln3 relaxin 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:19416195 1551268 Rln3 relaxin 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21887138 1551268 Rln3 relaxin 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19416195 1551268 Rln3 relaxin 3 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:21887138 1551268 Rln3 relaxin 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20161201 MGI 1551268 Rln3 relaxin 3 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:19416195 1551268 Rln3 relaxin 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19416196 1551268 Rln3 relaxin 3 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1551268 Rln3 relaxin 3 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1551268 Rln3 relaxin 3 gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:21887138 1551268 Rln3 relaxin 3 gene MP:0004892 increased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:19416196 1551268 Rln3 relaxin 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19416196 1551268 Rln3 relaxin 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19416196 1551268 Rln3 relaxin 3 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20211021 MGI 1551268 Rln3 relaxin 3 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19416196 1551268 Rln3 relaxin 3 gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19416196 1551268 Rln3 relaxin 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1551268 Rln3 relaxin 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19416196 1551268 Rln3 relaxin 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1551270 Strada STE20-related kinase adaptor alpha gene MP:0000111 cleft palate IEA N RGD:5509061 20230119 MGI 1551270 Strada STE20-related kinase adaptor alpha gene MP:0000120 malocclusion IAGP N RGD:5509061 20210923 MGI PMID:32457579 1551270 Strada STE20-related kinase adaptor alpha gene MP:0000440 domed cranium IAGP N RGD:5509061 20210923 MGI PMID:32457579 1551270 Strada STE20-related kinase adaptor alpha gene MP:0000745 tremors IAGP N RGD:5509061 20210923 MGI PMID:32457579 1551270 Strada STE20-related kinase adaptor alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20210923 MGI PMID:32457579 1551270 Strada STE20-related kinase adaptor alpha gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20210923 MGI PMID:32457579 1551270 Strada STE20-related kinase adaptor alpha gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20210923 MGI PMID:32457579 1551270 Strada STE20-related kinase adaptor alpha gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20210923 MGI PMID:32457579 1551270 Strada STE20-related kinase adaptor alpha gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20230119 MGI 1551270 Strada STE20-related kinase adaptor alpha gene MP:0004144 hypotonia IAGP N RGD:5509061 20210923 MGI PMID:32457579 1551270 Strada STE20-related kinase adaptor alpha gene MP:0004831 long incisors IAGP N RGD:5509061 20210923 MGI PMID:32457579 1551270 Strada STE20-related kinase adaptor alpha gene MP:0005238 increased brain size IAGP N RGD:5509061 20210923 MGI PMID:32457579 1551270 Strada STE20-related kinase adaptor alpha gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20210923 MGI PMID:32457579 1551270 Strada STE20-related kinase adaptor alpha gene MP:0009908 protruding tongue IEA N RGD:5509061 20230119 MGI 1551270 Strada STE20-related kinase adaptor alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210923 MGI PMID:32457579 1551270 Strada STE20-related kinase adaptor alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1551270 Strada STE20-related kinase adaptor alpha gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20210923 MGI PMID:32457579 1551270 Strada STE20-related kinase adaptor alpha gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20210923 MGI PMID:32457579 1551273 Sesn3 sestrin 3 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20160804 MGI 1551273 Sesn3 sestrin 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22958918 1551273 Sesn3 sestrin 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22958918 1551273 Sesn3 sestrin 3 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160804 MGI 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0000440 domed cranium IAGP N RGD:5509061 20200310 MGI PMID:23472195 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:23097495 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20200310 MGI PMID:23097495 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200310 MGI PMID:23097495 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20200310 MGI PMID:21746835 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20200310 MGI PMID:21746835 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20200310 MGI 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:21746835 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:23097495 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:23472195 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:23472195 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20200310 MGI PMID:23472195 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20200310 MGI PMID:23472195 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200310 MGI PMID:21746835 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21746835 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:23097495 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:23472195 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200310 MGI PMID:23472195 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:23097495 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0005202 lethargy IAGP N RGD:5509061 20200310 MGI PMID:23472195 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:23097495 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:23097495 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20200310 MGI PMID:23097495 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20200310 MGI PMID:23097495 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20200310 MGI PMID:23097495 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20200310 MGI PMID:23097495 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23472195 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23097495 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23472195 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23097495 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551274 Mboat7 membrane bound O-acyltransferase domain containing 7 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20200310 MGI PMID:21746835 1551275 Dcps decapping enzyme, scavenger gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1551275 Dcps decapping enzyme, scavenger gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551275 Dcps decapping enzyme, scavenger gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551280 H2-T24 histocompatibility 2, T region locus 24 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1551280 H2-T24 histocompatibility 2, T region locus 24 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1551280 H2-T24 histocompatibility 2, T region locus 24 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 1551281 Myo9a myosin IXa gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20180322 MGI PMID:19828736 1551281 Myo9a myosin IXa gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20180322 MGI PMID:19828736 1551281 Myo9a myosin IXa gene MP:0000917 obstructive hydrocephaly IAGP N RGD:5509061 20180322 MGI PMID:19828736 1551281 Myo9a myosin IXa gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1551281 Myo9a myosin IXa gene MP:0001393 ataxia IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0001406 abnormal gait IAGP N RGD:5509061 20180322 MGI PMID:19828736 1551281 Myo9a myosin IXa gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180322 MGI PMID:19828736 1551281 Myo9a myosin IXa gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0002064 seizures IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0002871 albuminuria IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0003584 bifid ureter IEA N RGD:5509061 20170504 MGI 1551281 Myo9a myosin IXa gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1551281 Myo9a myosin IXa gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20170504 MGI 1551281 Myo9a myosin IXa gene MP:0004160 retroesophageal right subclavian artery IEA N RGD:5509061 20170504 MGI 1551281 Myo9a myosin IXa gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1551281 Myo9a myosin IXa gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20180322 MGI PMID:19828736 1551281 Myo9a myosin IXa gene MP:0006093 arteriovenous malformation IEA N RGD:5509061 20170504 MGI 1551281 Myo9a myosin IXa gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20180322 MGI PMID:19828736 1551281 Myo9a myosin IXa gene MP:0009689 abnormal neural tube ventricular layer morphology IAGP N RGD:5509061 20180322 MGI PMID:19828736 1551281 Myo9a myosin IXa gene MP:0011293 dilated nephron IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0011864 abnormal podocyte adhesion IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0011867 decreased podocyte motility IAGP N RGD:5509061 20210422 MGI PMID:33412162 1551281 Myo9a myosin IXa gene MP:0013228 brain ventricle stenosis IAGP N RGD:5509061 20180322 MGI PMID:19828736 1551281 Myo9a myosin IXa gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1551281 Myo9a myosin IXa gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20170504 MGI 1551281 Myo9a myosin IXa gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1551283 Rarres1 retinoic acid receptor responder (tazarotene induced) 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20220721 MGI PMID:35541897 1551283 Rarres1 retinoic acid receptor responder (tazarotene induced) 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20220721 MGI PMID:35541897 1551283 Rarres1 retinoic acid receptor responder (tazarotene induced) 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20220721 MGI PMID:35541897 1551283 Rarres1 retinoic acid receptor responder (tazarotene induced) 1 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20220721 MGI PMID:35541897 1551283 Rarres1 retinoic acid receptor responder (tazarotene induced) 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20220721 MGI PMID:35541897 1551283 Rarres1 retinoic acid receptor responder (tazarotene induced) 1 gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20220721 MGI PMID:35541897 1551283 Rarres1 retinoic acid receptor responder (tazarotene induced) 1 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20220721 MGI PMID:35541897 1551283 Rarres1 retinoic acid receptor responder (tazarotene induced) 1 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20220721 MGI PMID:35541897 1551283 Rarres1 retinoic acid receptor responder (tazarotene induced) 1 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20220721 MGI PMID:35541897 1551283 Rarres1 retinoic acid receptor responder (tazarotene induced) 1 gene MP:0009317 increased follicular lymphoma incidence IAGP N RGD:5509061 20220721 MGI PMID:35541897 1551283 Rarres1 retinoic acid receptor responder (tazarotene induced) 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20220721 MGI PMID:35541897 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20231207 MGI 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:12149515 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210422 MGI 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12149515 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20231207 MGI 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12149515 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12149515 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12149515 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17360959 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20160804 MGI PMID:25614626 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0008839 absent acrosome IAGP N RGD:5509061 20141003 MGI PMID:12149515 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17360959 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:12149515 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0009231 detached acrosome IAGP N RGD:5509061 20141003 MGI PMID:12149515 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:12149515 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:12149515 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:17360959 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0009476 enlarged cecum IEA N RGD:5509061 20210422 MGI 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:12149515 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20160804 MGI PMID:25614626 1551284 Gopc golgi associated PDZ and coiled-coil motif containing gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210422 MGI 1551286 Ccser2 coiled-coil serine rich 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20230601 MGI PMID:36795749 1551286 Ccser2 coiled-coil serine rich 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20230601 MGI PMID:36795749 1551286 Ccser2 coiled-coil serine rich 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20230601 MGI PMID:36795749 1551289 Ppm1h protein phosphatase 1H (PP2C domain containing) gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20211125 MGI PMID:34658337 1551298 Ppic peptidylprolyl isomerase C gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20220317 MGI PMID:33864384 1551298 Ppic peptidylprolyl isomerase C gene MP:0009922 increased transitional stage T1 B cell number IAGP N RGD:5509061 20220317 MGI PMID:33864384 1551298 Ppic peptidylprolyl isomerase C gene MP:0009925 increased transitional stage T2 B cell number IAGP N RGD:5509061 20220317 MGI PMID:33864384 1551300 Timm8a1 translocase of inner mitochondrial membrane 8A1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20221215 MGI 1551300 Timm8a1 translocase of inner mitochondrial membrane 8A1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20221215 MGI 1551300 Timm8a1 translocase of inner mitochondrial membrane 8A1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 1551300 Timm8a1 translocase of inner mitochondrial membrane 8A1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20221215 MGI 1551300 Timm8a1 translocase of inner mitochondrial membrane 8A1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1551301 Aicda activation-induced cytidine deaminase gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1551301 Aicda activation-induced cytidine deaminase gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:22117047 1551301 Aicda activation-induced cytidine deaminase gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:21258321 1551301 Aicda activation-induced cytidine deaminase gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:21258321 1551301 Aicda activation-induced cytidine deaminase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 1551301 Aicda activation-induced cytidine deaminase gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 1551301 Aicda activation-induced cytidine deaminase gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 1551301 Aicda activation-induced cytidine deaminase gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 1551301 Aicda activation-induced cytidine deaminase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19808965 1551301 Aicda activation-induced cytidine deaminase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22117047 1551301 Aicda activation-induced cytidine deaminase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19855380 1551301 Aicda activation-induced cytidine deaminase gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20230810 MGI PMID:33098766 1551301 Aicda activation-induced cytidine deaminase gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21258321 1551301 Aicda activation-induced cytidine deaminase gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19070574 1551301 Aicda activation-induced cytidine deaminase gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20133609 1551301 Aicda activation-induced cytidine deaminase gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:22117047 1551301 Aicda activation-induced cytidine deaminase gene MP:0002492 decreased IgE level IEA N RGD:5509061 20181011 MGI 1551301 Aicda activation-induced cytidine deaminase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11007474 1551301 Aicda activation-induced cytidine deaminase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21258321 1551301 Aicda activation-induced cytidine deaminase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20230810 MGI PMID:33098766 1551301 Aicda activation-induced cytidine deaminase gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:19070574 1551301 Aicda activation-induced cytidine deaminase gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:19587764 1551301 Aicda activation-induced cytidine deaminase gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:19070574 1551301 Aicda activation-induced cytidine deaminase gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:18455451 1551301 Aicda activation-induced cytidine deaminase gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:18838546 1551301 Aicda activation-induced cytidine deaminase gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:19196992 1551301 Aicda activation-induced cytidine deaminase gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:21258321 1551301 Aicda activation-induced cytidine deaminase gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:22962683 1551301 Aicda activation-induced cytidine deaminase gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20210513 MGI PMID:33526923 1551301 Aicda activation-induced cytidine deaminase gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:11007474 1551301 Aicda activation-induced cytidine deaminase gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:12810694 1551301 Aicda activation-induced cytidine deaminase gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:18455451 1551301 Aicda activation-induced cytidine deaminase gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:18838546 1551301 Aicda activation-induced cytidine deaminase gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:19196992 1551301 Aicda activation-induced cytidine deaminase gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:20368578 1551301 Aicda activation-induced cytidine deaminase gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20230810 MGI PMID:33098766 1551301 Aicda activation-induced cytidine deaminase gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1551301 Aicda activation-induced cytidine deaminase gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 1551301 Aicda activation-induced cytidine deaminase gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 1551301 Aicda activation-induced cytidine deaminase gene MP:0008094 absent memory B cells IAGP N RGD:5509061 20141003 MGI PMID:22117047 1551301 Aicda activation-induced cytidine deaminase gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:22117047 1551301 Aicda activation-induced cytidine deaminase gene MP:0008100 absent plasma cells IAGP N RGD:5509061 20141003 MGI PMID:22117047 1551301 Aicda activation-induced cytidine deaminase gene MP:0008174 decreased follicular B cell number IEA N RGD:5509061 20201231 MGI 1551301 Aicda activation-induced cytidine deaminase gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21258321 1551301 Aicda activation-induced cytidine deaminase gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:22117047 1551301 Aicda activation-induced cytidine deaminase gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22117047 1551301 Aicda activation-induced cytidine deaminase gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11007474 1551301 Aicda activation-induced cytidine deaminase gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:21258321 1551301 Aicda activation-induced cytidine deaminase gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:11007474 1551301 Aicda activation-induced cytidine deaminase gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:21258321 1551301 Aicda activation-induced cytidine deaminase gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:21258321 1551301 Aicda activation-induced cytidine deaminase gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:23254285 1551301 Aicda activation-induced cytidine deaminase gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20230810 MGI PMID:33098766 1551301 Aicda activation-induced cytidine deaminase gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20230810 MGI PMID:33098766 1551301 Aicda activation-induced cytidine deaminase gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:18455451 1551301 Aicda activation-induced cytidine deaminase gene MP:0009317 increased follicular lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 1551301 Aicda activation-induced cytidine deaminase gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 1551301 Aicda activation-induced cytidine deaminase gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21258321 1551301 Aicda activation-induced cytidine deaminase gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 1551301 Aicda activation-induced cytidine deaminase gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20141003 MGI PMID:21258321 1551301 Aicda activation-induced cytidine deaminase gene MP:0013684 increased early germinal center B cell number IEA N RGD:5509061 20201231 MGI 1551301 Aicda activation-induced cytidine deaminase gene MP:0013685 decreased late germinal center B cell number IEA N RGD:5509061 20201231 MGI 1551303 Rnf41 ring finger protein 41 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 1551303 Rnf41 ring finger protein 41 gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 1551303 Rnf41 ring finger protein 41 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20220519 MGI 1551304 Tmem63a transmembrane protein 63a gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 1551306 Cfdp1 craniofacial development protein 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20240905 MGI PMID:38630655 1551306 Cfdp1 craniofacial development protein 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20240905 MGI PMID:38630655 1551306 Cfdp1 craniofacial development protein 1 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20240905 MGI PMID:38630655 1551306 Cfdp1 craniofacial development protein 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20240905 MGI PMID:38630655 1551306 Cfdp1 craniofacial development protein 1 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20240905 MGI PMID:38630655 1551306 Cfdp1 craniofacial development protein 1 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20240905 MGI PMID:38630655 1551306 Cfdp1 craniofacial development protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1551306 Cfdp1 craniofacial development protein 1 gene MP:0012174 flat head IAGP N RGD:5509061 20240905 MGI PMID:38630655 1551306 Cfdp1 craniofacial development protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1551306 Cfdp1 craniofacial development protein 1 gene MP:0014241 abnormal intracellular organelle physiology IAGP N RGD:5509061 20240905 MGI PMID:38630655 1551307 Zbtb7a zinc finger and BTB domain containing 7a gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:17495164 1551307 Zbtb7a zinc finger and BTB domain containing 7a gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:17495164 1551307 Zbtb7a zinc finger and BTB domain containing 7a gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20200310 MGI PMID:17495164 1551307 Zbtb7a zinc finger and BTB domain containing 7a gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:17495164 1551307 Zbtb7a zinc finger and BTB domain containing 7a gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20200310 MGI PMID:17495164 1551307 Zbtb7a zinc finger and BTB domain containing 7a gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:17495164 1551307 Zbtb7a zinc finger and BTB domain containing 7a gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20200310 MGI PMID:17495164 1551307 Zbtb7a zinc finger and BTB domain containing 7a gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20200310 MGI PMID:17495164 1551307 Zbtb7a zinc finger and BTB domain containing 7a gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17495164 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0000599 enlarged liver IEA N RGD:5509061 20210520 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0002188 small heart IEA N RGD:5509061 20210826 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210826 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1551308 Gapvd1 GTPase activating protein and VPS9 domains 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1551310 Commd3 COMM domain containing 3 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20190912 MGI PMID:31088898 1551310 Commd3 COMM domain containing 3 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20190912 MGI PMID:31088898 1551310 Commd3 COMM domain containing 3 gene MP:0008191 abnormal follicular B cell physiology IAGP N RGD:5509061 20190912 MGI PMID:31088898 1551310 Commd3 COMM domain containing 3 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20190912 MGI PMID:31088898 1551310 Commd3 COMM domain containing 3 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20190912 MGI PMID:31088898 1551310 Commd3 COMM domain containing 3 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20190912 MGI PMID:31088898 1551310 Commd3 COMM domain containing 3 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20190912 MGI PMID:31088898 1551310 Commd3 COMM domain containing 3 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20190912 MGI PMID:31088898 1551310 Commd3 COMM domain containing 3 gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20190912 MGI PMID:31088898 1551310 Commd3 COMM domain containing 3 gene MP:0013940 abnormal plasmablast number IAGP N RGD:5509061 20190912 MGI PMID:31088898 1551312 Aldh3b1 aldehyde dehydrogenase 3 family, member B1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160421 MGI 1551312 Aldh3b1 aldehyde dehydrogenase 3 family, member B1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 1551312 Aldh3b1 aldehyde dehydrogenase 3 family, member B1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16276414 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:8018921 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18765677 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8018921 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8018921 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8018921 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8171324 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8202532 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:10684813 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:8171324 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:8202532 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16276414 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18765677 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:16276414 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16276414 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16276414 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17483299 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12732663 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:11159518 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:8018921 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:8202532 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:8018921 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20141003 MGI PMID:10684813 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:8202532 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12732663 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12732663 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17483299 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12732663 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8018921 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002224 abnormal spleen size IAGP N RGD:5509061 20141003 MGI PMID:11119498 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:8018921 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:8171324 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:8202532 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:8018921 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8202532 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10684813 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:12732663 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12732663 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12732663 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18765677 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:12732663 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:8018921 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12890699 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:17483299 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0003356 impaired luteinization IAGP N RGD:5509061 20141003 MGI PMID:10684813 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12732663 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10684813 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:12732663 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:11159518 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:12732663 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:19196868 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:10684813 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:16276414 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11159518 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12732663 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:11119498 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0005040 abnormal MHC II cell surface expression on macrophages IAGP N RGD:5509061 20141003 MGI PMID:10684813 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:10684813 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:17483299 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17483299 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:8202532 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17483299 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:8018921 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11159518 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16276414 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:21262803 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141211 MGI PMID:24633240 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:18765677 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:8171324 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:8202532 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12732663 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0008903 abnormal mesenteric fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18765677 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:10684813 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:10684813 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0009020 prolonged metestrus IAGP N RGD:5509061 20141003 MGI PMID:10684813 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16276414 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16276414 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16276414 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16276414 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0010998 pulmonary alveolar proteinosis IAGP N RGD:5509061 20141003 MGI PMID:8018921 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0010998 pulmonary alveolar proteinosis IAGP N RGD:5509061 20141003 MGI PMID:8202532 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12732663 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0011640 abnormal aorta collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:12890699 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:16276414 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0012098 increased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0012109 decreased trophoblast glycogen cell number IAGP N RGD:5509061 20141003 MGI PMID:9915988 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20170202 MGI PMID:16276414 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:8018921 1551314 Csf2 colony stimulating factor 2 (granulocyte-macrophage) gene MP:0030974 enhanced gluconeogenesis IAGP N RGD:5509061 20200102 MGI PMID:18765677 1551315 Slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:17035501 1551315 Slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17035501 1551315 Slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17035501 1551315 Slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:17035501 1551315 Slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17035501 1551315 Slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17035501 1551315 Slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:17035501 1551315 Slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17035501 1551315 Slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene MP:0002893 ketoaciduria IAGP N RGD:5509061 20141003 MGI PMID:17035501 1551315 Slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17035501 1551315 Slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:17035501 1551315 Slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17035501 1551315 Slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene MP:0012172 abnormal amniotic fluid composition IAGP N RGD:5509061 20141003 MGI PMID:17035501 1551315 Slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene MP:0012677 absent brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:17035501 1551315 Slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:17035501 1551318 Dnajc7 DnaJ heat shock protein family (Hsp40) member C7 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 1551318 Dnajc7 DnaJ heat shock protein family (Hsp40) member C7 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1551318 Dnajc7 DnaJ heat shock protein family (Hsp40) member C7 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160407 MGI PMID:25542016 1551318 Dnajc7 DnaJ heat shock protein family (Hsp40) member C7 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20160407 MGI PMID:25542016 1551318 Dnajc7 DnaJ heat shock protein family (Hsp40) member C7 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1551319 Angel2 angel homolog 2 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20230223 MGI PMID:36180430 1551319 Angel2 angel homolog 2 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20230223 MGI PMID:36180430 1551319 Angel2 angel homolog 2 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20230223 MGI PMID:36180430 1551319 Angel2 angel homolog 2 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20230223 MGI PMID:36180430 1551322 Klk4 kallikrein related-peptidase 4 (prostase, enamel matrix, prostate) gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1551322 Klk4 kallikrein related-peptidase 4 (prostase, enamel matrix, prostate) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19578120 1551322 Klk4 kallikrein related-peptidase 4 (prostase, enamel matrix, prostate) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19578120 1551322 Klk4 kallikrein related-peptidase 4 (prostase, enamel matrix, prostate) gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:19578120 1551322 Klk4 kallikrein related-peptidase 4 (prostase, enamel matrix, prostate) gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1551322 Klk4 kallikrein related-peptidase 4 (prostase, enamel matrix, prostate) gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 1551327 Irf6 interferon regulatory factor 6 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0000111 cleft palate IAGP N RGD:5509061 20151210 MGI PMID:24360809 1551327 Irf6 interferon regulatory factor 6 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:22366192 1551327 Irf6 interferon regulatory factor 6 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20141003 MGI PMID:20196077 1551327 Irf6 interferon regulatory factor 6 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0000467 abnormal esophagus morphology IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:20196077 1551327 Irf6 interferon regulatory factor 6 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:20196077 1551327 Irf6 interferon regulatory factor 6 gene MP:0000566 synostosis IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0001241 absent epidermis stratum corneum IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0001241 absent epidermis stratum corneum IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0002649 abnormal enamel rod pattern IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:20196077 1551327 Irf6 interferon regulatory factor 6 gene MP:0003160 abnormal esophagus development IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0003385 abnormal body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0003932 abnormal molar crown morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:22366192 1551327 Irf6 interferon regulatory factor 6 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20151210 MGI PMID:24360809 1551327 Irf6 interferon regulatory factor 6 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20141003 MGI PMID:21918538 1551327 Irf6 interferon regulatory factor 6 gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0004537 abnormal palatine bone horizontal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20196077 1551327 Irf6 interferon regulatory factor 6 gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20171019 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1551327 Irf6 interferon regulatory factor 6 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:22366192 1551327 Irf6 interferon regulatory factor 6 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:20196077 1551327 Irf6 interferon regulatory factor 6 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210520 MGI 1551327 Irf6 interferon regulatory factor 6 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0006400 decreased molar number IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:20196077 1551327 Irf6 interferon regulatory factor 6 gene MP:0009441 delayed skin barrier formation IAGP N RGD:5509061 20141003 MGI PMID:20196077 1551327 Irf6 interferon regulatory factor 6 gene MP:0009474 thick epidermis stratum spinosum IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0009560 absent epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0009560 absent epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20151210 MGI PMID:24360809 1551327 Irf6 interferon regulatory factor 6 gene MP:0009884 palatal shelf fusion with tongue or mandible IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0009884 palatal shelf fusion with tongue or mandible IAGP N RGD:5509061 20141003 MGI PMID:20196077 1551327 Irf6 interferon regulatory factor 6 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:20196077 1551327 Irf6 interferon regulatory factor 6 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:20196077 1551327 Irf6 interferon regulatory factor 6 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 1551327 Irf6 interferon regulatory factor 6 gene MP:0010096 abnormal incisor color IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20151210 MGI PMID:24360809 1551327 Irf6 interferon regulatory factor 6 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17041603 1551327 Irf6 interferon regulatory factor 6 gene MP:0011089 perinatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1551327 Irf6 interferon regulatory factor 6 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20151210 MGI PMID:24360809 1551327 Irf6 interferon regulatory factor 6 gene MP:0013531 abnormal periderm development IAGP N RGD:5509061 20151210 MGI PMID:24360809 1551327 Irf6 interferon regulatory factor 6 gene MP:0013818 abnormal oral cavity morphology IAGP N RGD:5509061 20151210 MGI PMID:24360809 1551327 Irf6 interferon regulatory factor 6 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:20196077 1551327 Irf6 interferon regulatory factor 6 gene MP:0030188 round snout IAGP N RGD:5509061 20171019 MGI PMID:17041601 1551327 Irf6 interferon regulatory factor 6 gene MP:0030328 glossopalatal ankylosis IAGP N RGD:5509061 20221103 MGI PMID:20196077 1551327 Irf6 interferon regulatory factor 6 gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0030494 abnormal molar root morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0030496 taurodontia IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0030525 abnormal Hertwig epithelial root sheath morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551327 Irf6 interferon regulatory factor 6 gene MP:0030544 abnormal enamel development IAGP N RGD:5509061 20190711 MGI PMID:27369589 1551328 Zfp142 zinc finger protein 142 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1551328 Zfp142 zinc finger protein 142 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1551333 Hpcal1 hippocalcin-like 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20221222 MGI PMID:36438486 1551333 Hpcal1 hippocalcin-like 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20221222 MGI PMID:36438486 1551333 Hpcal1 hippocalcin-like 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20221222 MGI PMID:36438486 1551333 Hpcal1 hippocalcin-like 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20221222 MGI PMID:36438486 1551333 Hpcal1 hippocalcin-like 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20221222 MGI PMID:36438486 1551333 Hpcal1 hippocalcin-like 1 gene MP:0030673 increased circulating alanine level IAGP N RGD:5509061 20221222 MGI PMID:36438486 1551337 Spink1 serine peptidase inhibitor, Kazal type 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:16083722 1551337 Spink1 serine peptidase inhibitor, Kazal type 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:16083722 1551337 Spink1 serine peptidase inhibitor, Kazal type 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:16083722 1551337 Spink1 serine peptidase inhibitor, Kazal type 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:16083722 1551337 Spink1 serine peptidase inhibitor, Kazal type 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16083722 1551337 Spink1 serine peptidase inhibitor, Kazal type 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:16083722 1551337 Spink1 serine peptidase inhibitor, Kazal type 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16083722 1551337 Spink1 serine peptidase inhibitor, Kazal type 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:16083722 1551337 Spink1 serine peptidase inhibitor, Kazal type 1 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:16083722 1551337 Spink1 serine peptidase inhibitor, Kazal type 1 gene MP:0005520 impaired pancreas regeneration IAGP N RGD:5509061 20141003 MGI PMID:16083722 1551337 Spink1 serine peptidase inhibitor, Kazal type 1 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16083722 1551337 Spink1 serine peptidase inhibitor, Kazal type 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16083722 1551337 Spink1 serine peptidase inhibitor, Kazal type 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18386042 1551338 Ift88 intraflagellar transport 88 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20200310 MGI PMID:12701101 1551338 Ift88 intraflagellar transport 88 gene MP:0000111 cleft palate IAGP N RGD:5509061 20200310 MGI PMID:22228099 1551338 Ift88 intraflagellar transport 88 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:17166921 1551338 Ift88 intraflagellar transport 88 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20210114 MGI PMID:32702291 1551338 Ift88 intraflagellar transport 88 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20240125 MGI PMID:30289203 1551338 Ift88 intraflagellar transport 88 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20210715 MGI PMID:31118289 1551338 Ift88 intraflagellar transport 88 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20200310 MGI PMID:17166921 1551338 Ift88 intraflagellar transport 88 gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:17166921 1551338 Ift88 intraflagellar transport 88 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20200310 MGI PMID:12701101 1551338 Ift88 intraflagellar transport 88 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:12701101 1551338 Ift88 intraflagellar transport 88 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:14603322 1551338 Ift88 intraflagellar transport 88 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:15755804 1551338 Ift88 intraflagellar transport 88 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:17166921 1551338 Ift88 intraflagellar transport 88 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:8191288 1551338 Ift88 intraflagellar transport 88 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:11773599 1551338 Ift88 intraflagellar transport 88 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20200310 MGI PMID:15755804 1551338 Ift88 intraflagellar transport 88 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20200310 MGI PMID:14603322 1551338 Ift88 intraflagellar transport 88 gene MP:0000898 midbrain hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:22228099 1551338 Ift88 intraflagellar transport 88 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20200310 MGI PMID:14603322 1551338 Ift88 intraflagellar transport 88 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20200310 MGI PMID:15755804 1551338 Ift88 intraflagellar transport 88 gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:17166921 1551338 Ift88 intraflagellar transport 88 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:17166921 1551338 Ift88 intraflagellar transport 88 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200310 MGI PMID:22228099 1551338 Ift88 intraflagellar transport 88 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20200310 MGI PMID:8191288 1551338 Ift88 intraflagellar transport 88 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200310 MGI 1551338 Ift88 intraflagellar transport 88 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20200310 MGI 1551338 Ift88 intraflagellar transport 88 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20200310 MGI PMID:15755804 1551338 Ift88 intraflagellar transport 88 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:14603322 1551338 Ift88 intraflagellar transport 88 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:8191288 1551338 Ift88 intraflagellar transport 88 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20210805 MGI PMID:34186026 1551338 Ift88 intraflagellar transport 88 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20200310 MGI PMID:22228099 1551338 Ift88 intraflagellar transport 88 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20200310 MGI PMID:11773599 1551338 Ift88 intraflagellar transport 88 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20200310 MGI PMID:15226261 1551338 Ift88 intraflagellar transport 88 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20200310 MGI PMID:17166921 1551338 Ift88 intraflagellar transport 88 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:17166921 1551338 Ift88 intraflagellar transport 88 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20200310 MGI PMID:17359961 1551338 Ift88 intraflagellar transport 88 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20240125 MGI PMID:30289203 1551338 Ift88 intraflagellar transport 88 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20200310 MGI PMID:15580285 1551338 Ift88 intraflagellar transport 88 gene MP:0002694 abnormal pancreas secretion IAGP N RGD:5509061 20200310 MGI PMID:15226261 1551338 Ift88 intraflagellar transport 88 gene MP:0002694 abnormal pancreas secretion IAGP N RGD:5509061 20200310 MGI PMID:15580285 1551338 Ift88 intraflagellar transport 88 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:17166921 1551338 Ift88 intraflagellar transport 88 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20200310 MGI PMID:11773599 1551338 Ift88 intraflagellar transport 88 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20200310 MGI PMID:8191288 1551338 Ift88 intraflagellar transport 88 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20200310 MGI PMID:8952527 1551338 Ift88 intraflagellar transport 88 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20200310 MGI PMID:11773599 1551338 Ift88 intraflagellar transport 88 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20200310 MGI PMID:11773599 1551338 Ift88 intraflagellar transport 88 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20200310 MGI PMID:17359961 1551338 Ift88 intraflagellar transport 88 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20200310 MGI PMID:8191288 1551338 Ift88 intraflagellar transport 88 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200310 MGI PMID:11773599 1551338 Ift88 intraflagellar transport 88 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200310 MGI PMID:8191288 1551338 Ift88 intraflagellar transport 88 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200310 MGI PMID:8952527 1551338 Ift88 intraflagellar transport 88 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20200310 MGI PMID:11773599 1551338 Ift88 intraflagellar transport 88 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20200310 MGI PMID:15226261 1551338 Ift88 intraflagellar transport 88 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20200310 MGI PMID:15580285 1551338 Ift88 intraflagellar transport 88 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0003462 abnormal response to novel odor IAGP N RGD:5509061 20210805 MGI PMID:34186026 1551338 Ift88 intraflagellar transport 88 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:11773599 1551338 Ift88 intraflagellar transport 88 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:8191288 1551338 Ift88 intraflagellar transport 88 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20200310 MGI PMID:12701101 1551338 Ift88 intraflagellar transport 88 gene MP:0003840 abnormal coronal suture morphology IAGP N RGD:5509061 20200310 MGI PMID:12701101 1551338 Ift88 intraflagellar transport 88 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20210114 MGI PMID:32702291 1551338 Ift88 intraflagellar transport 88 gene MP:0004203 abnormal cranial flexure morphology IAGP N RGD:5509061 20200310 MGI PMID:14603322 1551338 Ift88 intraflagellar transport 88 gene MP:0004247 small pancreas IAGP N RGD:5509061 20200310 MGI PMID:15226261 1551338 Ift88 intraflagellar transport 88 gene MP:0004247 small pancreas IAGP N RGD:5509061 20200310 MGI PMID:15580285 1551338 Ift88 intraflagellar transport 88 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0004574 broad limb buds IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0004574 broad limb buds IAGP N RGD:5509061 20200310 MGI PMID:22228099 1551338 Ift88 intraflagellar transport 88 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20200310 MGI PMID:17166921 1551338 Ift88 intraflagellar transport 88 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20200310 MGI PMID:11773599 1551338 Ift88 intraflagellar transport 88 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20200310 MGI PMID:17166921 1551338 Ift88 intraflagellar transport 88 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20200310 MGI PMID:12701101 1551338 Ift88 intraflagellar transport 88 gene MP:0005262 coloboma IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:15580285 1551338 Ift88 intraflagellar transport 88 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20200310 MGI PMID:12701101 1551338 Ift88 intraflagellar transport 88 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20210114 MGI PMID:32702291 1551338 Ift88 intraflagellar transport 88 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:15580285 1551338 Ift88 intraflagellar transport 88 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20200310 MGI PMID:12701101 1551338 Ift88 intraflagellar transport 88 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20200310 MGI PMID:17166921 1551338 Ift88 intraflagellar transport 88 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20200310 MGI PMID:22228099 1551338 Ift88 intraflagellar transport 88 gene MP:0006322 abnormal perichondrium morphology IAGP N RGD:5509061 20200310 MGI PMID:17166921 1551338 Ift88 intraflagellar transport 88 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20200310 MGI PMID:17166921 1551338 Ift88 intraflagellar transport 88 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20200310 MGI PMID:17166921 1551338 Ift88 intraflagellar transport 88 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20200310 MGI PMID:11773599 1551338 Ift88 intraflagellar transport 88 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20200310 MGI PMID:8191288 1551338 Ift88 intraflagellar transport 88 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20200310 MGI PMID:8191288 1551338 Ift88 intraflagellar transport 88 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20200310 MGI PMID:8952527 1551338 Ift88 intraflagellar transport 88 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0009143 abnormal pancreatic duct morphology IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0009143 abnormal pancreatic duct morphology IAGP N RGD:5509061 20200310 MGI PMID:11773599 1551338 Ift88 intraflagellar transport 88 gene MP:0009143 abnormal pancreatic duct morphology IAGP N RGD:5509061 20200310 MGI PMID:15226261 1551338 Ift88 intraflagellar transport 88 gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20200310 MGI PMID:15580285 1551338 Ift88 intraflagellar transport 88 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15226261 1551338 Ift88 intraflagellar transport 88 gene MP:0009149 decreased pancreatic acinar cell number IAGP N RGD:5509061 20200310 MGI PMID:11773599 1551338 Ift88 intraflagellar transport 88 gene MP:0009150 pancreatic acinar cell atrophy IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20200310 MGI PMID:31226309 1551338 Ift88 intraflagellar transport 88 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20200310 MGI PMID:14603322 1551338 Ift88 intraflagellar transport 88 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20200310 MGI PMID:12701101 1551338 Ift88 intraflagellar transport 88 gene MP:0010041 absent oval cells IAGP N RGD:5509061 20200310 MGI PMID:11773599 1551338 Ift88 intraflagellar transport 88 gene MP:0010042 abnormal oval cell physiology IAGP N RGD:5509061 20200310 MGI PMID:8191288 1551338 Ift88 intraflagellar transport 88 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0010406 common atrium IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20240125 MGI PMID:30289203 1551338 Ift88 intraflagellar transport 88 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20240125 MGI PMID:30289203 1551338 Ift88 intraflagellar transport 88 gene MP:0010436 abnormal coronary sinus morphology IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0010440 anomalous pulmonary venous connection IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0010440 anomalous pulmonary venous connection IAGP N RGD:5509061 20240125 MGI PMID:30289203 1551338 Ift88 intraflagellar transport 88 gene MP:0010521 absent pulmonary artery IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0010548 abnormal dorsal mesocardium morphology IAGP N RGD:5509061 20240125 MGI PMID:30289203 1551338 Ift88 intraflagellar transport 88 gene MP:0010614 abnormal mitral valve cusp morphology IAGP N RGD:5509061 20210715 MGI PMID:31118289 1551338 Ift88 intraflagellar transport 88 gene MP:0010773 supernumerary molars IAGP N RGD:5509061 20200310 MGI PMID:12701101 1551338 Ift88 intraflagellar transport 88 gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20200310 MGI PMID:11062270 1551338 Ift88 intraflagellar transport 88 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:8191288 1551338 Ift88 intraflagellar transport 88 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:8952527 1551338 Ift88 intraflagellar transport 88 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10804177 1551338 Ift88 intraflagellar transport 88 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:14603322 1551338 Ift88 intraflagellar transport 88 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15755804 1551338 Ift88 intraflagellar transport 88 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22228099 1551338 Ift88 intraflagellar transport 88 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551338 Ift88 intraflagellar transport 88 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19036983 1551338 Ift88 intraflagellar transport 88 gene MP:0012531 delayed limb development IAGP N RGD:5509061 20200310 MGI PMID:22228099 1551338 Ift88 intraflagellar transport 88 gene MP:0013206 abnormal motile cilium morphology IAGP N RGD:5509061 20210715 MGI PMID:31118289 1551338 Ift88 intraflagellar transport 88 gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20210114 MGI PMID:32702291 1551338 Ift88 intraflagellar transport 88 gene MP:0014093 decreased pancreatic primary cilium length IAGP N RGD:5509061 20200310 MGI PMID:15226261 1551338 Ift88 intraflagellar transport 88 gene MP:0014093 decreased pancreatic primary cilium length IAGP N RGD:5509061 20200310 MGI PMID:15580285 1551338 Ift88 intraflagellar transport 88 gene MP:0014094 decreased pancreatic primary cilium number IAGP N RGD:5509061 20200310 MGI PMID:15226261 1551338 Ift88 intraflagellar transport 88 gene MP:0014094 decreased pancreatic primary cilium number IAGP N RGD:5509061 20200310 MGI PMID:15580285 1551340 Dnajc28 DnaJ heat shock protein family (Hsp40) member C28 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1551340 Dnajc28 DnaJ heat shock protein family (Hsp40) member C28 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20160421 MGI 1551341 Cd209c CD209c antigen gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1551341 Cd209c CD209c antigen gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 1551341 Cd209c CD209c antigen gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20240523 MGI 1551344 Gucy2g guanylate cyclase 2g gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:18199799 1551347 Myo1f myosin IF gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:17023661 1551347 Myo1f myosin IF gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17023661 1551348 Man1a2 mannosidase, alpha, class 1A, member 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20200310 MGI PMID:17121831 1551348 Man1a2 mannosidase, alpha, class 1A, member 2 gene MP:0001177 atelectasis IAGP N RGD:5509061 20200310 MGI PMID:17121831 1551348 Man1a2 mannosidase, alpha, class 1A, member 2 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20200310 MGI PMID:17121831 1551348 Man1a2 mannosidase, alpha, class 1A, member 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:17121831 1551348 Man1a2 mannosidase, alpha, class 1A, member 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:17121831 1551348 Man1a2 mannosidase, alpha, class 1A, member 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20200310 MGI PMID:17121831 1551348 Man1a2 mannosidase, alpha, class 1A, member 2 gene MP:0010909 pulmonary alveolar hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:17121831 1551348 Man1a2 mannosidase, alpha, class 1A, member 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17121831 1551349 Nek2 NIMA (never in mitosis gene a)-related expressed kinase 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1551349 Nek2 NIMA (never in mitosis gene a)-related expressed kinase 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 1551349 Nek2 NIMA (never in mitosis gene a)-related expressed kinase 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1551349 Nek2 NIMA (never in mitosis gene a)-related expressed kinase 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1551349 Nek2 NIMA (never in mitosis gene a)-related expressed kinase 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1551349 Nek2 NIMA (never in mitosis gene a)-related expressed kinase 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1551350 Ganab alpha glucosidase 2 alpha neutral subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210506 MGI PMID:32550232 1551350 Ganab alpha glucosidase 2 alpha neutral subunit gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20210506 MGI PMID:32550232 1551351 St3gal2 ST3 beta-galactoside alpha-2,3-sialyltransferase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:12393657 1551351 St3gal2 ST3 beta-galactoside alpha-2,3-sialyltransferase 2 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20200310 MGI PMID:23118208 1551351 St3gal2 ST3 beta-galactoside alpha-2,3-sialyltransferase 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:23118208 1551351 St3gal2 ST3 beta-galactoside alpha-2,3-sialyltransferase 2 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20200310 MGI PMID:23118208 1551351 St3gal2 ST3 beta-galactoside alpha-2,3-sialyltransferase 2 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20200310 MGI PMID:23118208 1551353 Polq polymerase (DNA directed), theta gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1551353 Polq polymerase (DNA directed), theta gene MP:0000692 small spleen IEA N RGD:5509061 20210128 MGI 1551353 Polq polymerase (DNA directed), theta gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16172387 1551353 Polq polymerase (DNA directed), theta gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16172387 1551353 Polq polymerase (DNA directed), theta gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20170713 MGI PMID:28570559 1551353 Polq polymerase (DNA directed), theta gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16172387 1551353 Polq polymerase (DNA directed), theta gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16172387 1551353 Polq polymerase (DNA directed), theta gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:12663541 1551353 Polq polymerase (DNA directed), theta gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:16172387 1551353 Polq polymerase (DNA directed), theta gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:16222339 1551353 Polq polymerase (DNA directed), theta gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:16890500 1551353 Polq polymerase (DNA directed), theta gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16172387 1551353 Polq polymerase (DNA directed), theta gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1551356 Thtpa thiamine triphosphatase gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1551356 Thtpa thiamine triphosphatase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1551356 Thtpa thiamine triphosphatase gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:7477376 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15863464 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15863464 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15863464 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0000296 absent trabeculae carneae IAGP N RGD:5509061 20141003 MGI PMID:7477376 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:7477376 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18203811 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:12824469 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:12954715 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12824469 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:18760695 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:7477376 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:7477376 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12824469 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7477376 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7477376 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7477376 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001072 abnormal vestibulocochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7477376 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7477376 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:7477376 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:7477376 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:7477376 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:18203811 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22378872 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12145742 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15863464 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18203811 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:12954715 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:18203811 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15863464 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20023653 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22378872 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0002271 abnormal pulmonary alveolar duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18203811 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20141003 MGI PMID:18203811 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15863464 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15863464 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15863464 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22378872 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:12145742 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:15863464 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:15863464 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:7477376 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:15863464 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:18203811 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:18203811 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:18203811 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:15863464 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:12824469 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:12954715 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:15863464 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:22378872 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22378872 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22378872 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12824469 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:15863464 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18760695 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12824469 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7477376 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0012757 abnormal cranial neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:12824469 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0013716 hypolactation IAGP N RGD:5509061 20150611 MGI PMID:12824469 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22378872 1551357 Erbb4 erb-b2 receptor tyrosine kinase 4 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15863464 1551360 Prkcq protein kinase C, theta gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15592506 1551360 Prkcq protein kinase C, theta gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20170126 MGI PMID:26978024 1551360 Prkcq protein kinase C, theta gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:15084656 1551360 Prkcq protein kinase C, theta gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170105 MGI 1551360 Prkcq protein kinase C, theta gene MP:0001147 small testis IEA N RGD:5509061 20170105 MGI 1551360 Prkcq protein kinase C, theta gene MP:0001267 enlarged chest IAGP N RGD:5509061 20141003 MGI PMID:15592506 1551360 Prkcq protein kinase C, theta gene MP:0001304 cataract IAGP N RGD:5509061 20170126 MGI PMID:26978024 1551360 Prkcq protein kinase C, theta gene MP:0001326 retina degeneration IAGP N RGD:5509061 20170720 MGI PMID:26978024 1551360 Prkcq protein kinase C, theta gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20170126 MGI PMID:26978024 1551360 Prkcq protein kinase C, theta gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:15592506 1551360 Prkcq protein kinase C, theta gene MP:0001805 decreased IgG level IEA N RGD:5509061 20180215 MGI 1551360 Prkcq protein kinase C, theta gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:10746729 1551360 Prkcq protein kinase C, theta gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1551360 Prkcq protein kinase C, theta gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15372106 1551360 Prkcq protein kinase C, theta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15592506 1551360 Prkcq protein kinase C, theta gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:15528385 1551360 Prkcq protein kinase C, theta gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22155788 1551360 Prkcq protein kinase C, theta gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12782715 1551360 Prkcq protein kinase C, theta gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20170126 MGI PMID:26978024 1551360 Prkcq protein kinase C, theta gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15372106 1551360 Prkcq protein kinase C, theta gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20141003 MGI PMID:15084656 1551360 Prkcq protein kinase C, theta gene MP:0003099 retina detachment IAGP N RGD:5509061 20170126 MGI PMID:26978024 1551360 Prkcq protein kinase C, theta gene MP:0003099 retina detachment IAGP N RGD:5509061 20170202 MGI PMID:27603725 1551360 Prkcq protein kinase C, theta gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20170202 MGI PMID:27603725 1551360 Prkcq protein kinase C, theta gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:15084656 1551360 Prkcq protein kinase C, theta gene MP:0004130 abnormal muscle cell glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:15372106 1551360 Prkcq protein kinase C, theta gene MP:0004185 abnormal adipocyte glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:15372106 1551360 Prkcq protein kinase C, theta gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16493044 1551360 Prkcq protein kinase C, theta gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:22155788 1551360 Prkcq protein kinase C, theta gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:15592506 1551360 Prkcq protein kinase C, theta gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17182568 1551360 Prkcq protein kinase C, theta gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:15024044 1551360 Prkcq protein kinase C, theta gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 1551360 Prkcq protein kinase C, theta gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 1551360 Prkcq protein kinase C, theta gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10746729 1551360 Prkcq protein kinase C, theta gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12782715 1551360 Prkcq protein kinase C, theta gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15024044 1551360 Prkcq protein kinase C, theta gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15528385 1551360 Prkcq protein kinase C, theta gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17182568 1551360 Prkcq protein kinase C, theta gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18155708 1551360 Prkcq protein kinase C, theta gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22155788 1551360 Prkcq protein kinase C, theta gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20170126 MGI PMID:26978024 1551360 Prkcq protein kinase C, theta gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20170720 MGI PMID:26978024 1551360 Prkcq protein kinase C, theta gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20170126 MGI PMID:26978024 1551360 Prkcq protein kinase C, theta gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15528385 1551360 Prkcq protein kinase C, theta gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:18815612 1551360 Prkcq protein kinase C, theta gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:15528385 1551360 Prkcq protein kinase C, theta gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20170126 MGI PMID:26978024 1551360 Prkcq protein kinase C, theta gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20170126 MGI PMID:26978024 1551360 Prkcq protein kinase C, theta gene MP:0006237 abnormal choroid vasculature morphology IAGP N RGD:5509061 20170202 MGI PMID:27603725 1551360 Prkcq protein kinase C, theta gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:18815612 1551360 Prkcq protein kinase C, theta gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20170126 MGI PMID:26978024 1551360 Prkcq protein kinase C, theta gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18842300 1551360 Prkcq protein kinase C, theta gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17182568 1551360 Prkcq protein kinase C, theta gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:18842300 1551360 Prkcq protein kinase C, theta gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 1551360 Prkcq protein kinase C, theta gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 1551360 Prkcq protein kinase C, theta gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15528385 1551360 Prkcq protein kinase C, theta gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20170202 MGI PMID:27603725 1551360 Prkcq protein kinase C, theta gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15528385 1551360 Prkcq protein kinase C, theta gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16493044 1551360 Prkcq protein kinase C, theta gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:15528385 1551360 Prkcq protein kinase C, theta gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:16493044 1551360 Prkcq protein kinase C, theta gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:10746729 1551360 Prkcq protein kinase C, theta gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:12782715 1551360 Prkcq protein kinase C, theta gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:15528385 1551360 Prkcq protein kinase C, theta gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:16493044 1551360 Prkcq protein kinase C, theta gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15528385 1551360 Prkcq protein kinase C, theta gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:16493044 1551360 Prkcq protein kinase C, theta gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:18155708 1551360 Prkcq protein kinase C, theta gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:15528385 1551360 Prkcq protein kinase C, theta gene MP:0008747 abnormal T cell anergy IAGP N RGD:5509061 20141003 MGI PMID:15024044 1551360 Prkcq protein kinase C, theta gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15528385 1551360 Prkcq protein kinase C, theta gene MP:0009274 buphthalmos IAGP N RGD:5509061 20170126 MGI PMID:26978024 1551360 Prkcq protein kinase C, theta gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15024044 1551360 Prkcq protein kinase C, theta gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16493044 1551360 Prkcq protein kinase C, theta gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20141003 MGI PMID:18815612 1551360 Prkcq protein kinase C, theta gene MP:0009586 increased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:18815612 1551360 Prkcq protein kinase C, theta gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20170126 MGI PMID:26978024 1551360 Prkcq protein kinase C, theta gene MP:0010130 decreased DN1 thymic pro-T cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 1551360 Prkcq protein kinase C, theta gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22155788 1551360 Prkcq protein kinase C, theta gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15592506 1551360 Prkcq protein kinase C, theta gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20180215 MGI 1551360 Prkcq protein kinase C, theta gene MP:0020442 serous retina detachment IAGP N RGD:5509061 20170907 MGI PMID:26978024 1551361 Vax1 ventral anterior homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10601035 1551361 Vax1 ventral anterior homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:15905411 1551361 Vax1 ventral anterior homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:15590934 1551361 Vax1 ventral anterior homeobox 1 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:10601035 1551361 Vax1 ventral anterior homeobox 1 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10601035 1551361 Vax1 ventral anterior homeobox 1 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15905411 1551361 Vax1 ventral anterior homeobox 1 gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:10601035 1551361 Vax1 ventral anterior homeobox 1 gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:15905411 1551361 Vax1 ventral anterior homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:10601035 1551361 Vax1 ventral anterior homeobox 1 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0002653 abnormal ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:15590934 1551361 Vax1 ventral anterior homeobox 1 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:15590934 1551361 Vax1 ventral anterior homeobox 1 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:10601035 1551361 Vax1 ventral anterior homeobox 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 1551361 Vax1 ventral anterior homeobox 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20211021 MGI 1551361 Vax1 ventral anterior homeobox 1 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:15905411 1551361 Vax1 ventral anterior homeobox 1 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15590934 1551361 Vax1 ventral anterior homeobox 1 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:15590934 1551361 Vax1 ventral anterior homeobox 1 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:15590934 1551361 Vax1 ventral anterior homeobox 1 gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0004450 presphenoid bone hypoplasia IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0004475 palatine bone hypoplasia IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0004790 absent upper incisors IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:10601035 1551361 Vax1 ventral anterior homeobox 1 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:15905411 1551361 Vax1 ventral anterior homeobox 1 gene MP:0005352 small cranium IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20181227 MGI 1551361 Vax1 ventral anterior homeobox 1 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0009771 absent optic chiasm IAGP N RGD:5509061 20141003 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0009898 maxillary shelf hypoplasia IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0009900 vomer bone hypoplasia IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15590934 1551361 Vax1 ventral anterior homeobox 1 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10601035 1551361 Vax1 ventral anterior homeobox 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15905411 1551361 Vax1 ventral anterior homeobox 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551361 Vax1 ventral anterior homeobox 1 gene MP:0011266 abnormal frontonasal mesenchyme morphology IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20231221 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0014276 lobar holoprosencephaly IAGP N RGD:5509061 20230810 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0030137 abnormal upper incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0030137 abnormal upper incisor morphology IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0030274 maxillary retrognathia IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551361 Vax1 ventral anterior homeobox 1 gene MP:0030476 fused upper incisors IAGP N RGD:5509061 20171228 MGI PMID:10601036 1551361 Vax1 ventral anterior homeobox 1 gene MP:0031457 abnormal vomeronasal cartilage morphology IAGP N RGD:5509061 20221215 MGI PMID:28771384 1551364 Zfp160 zinc finger protein 160 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1551364 Zfp160 zinc finger protein 160 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1551364 Zfp160 zinc finger protein 160 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220519 MGI 1551364 Zfp160 zinc finger protein 160 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 1551364 Zfp160 zinc finger protein 160 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1551365 Ctnnd2 catenin delta 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15380068 1551365 Ctnnd2 catenin delta 2 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15380068 1551365 Ctnnd2 catenin delta 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15380068 1551365 Ctnnd2 catenin delta 2 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15380068 1551365 Ctnnd2 catenin delta 2 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:15380068 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20191107 MGI PMID:27229483 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20191107 MGI PMID:27229483 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20200402 MGI 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0008168 decreased B-1a cell number IEA N RGD:5509061 20201231 MGI 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0008174 decreased follicular B cell number IEA N RGD:5509061 20201231 MGI 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0008211 decreased mature B cell number IEA N RGD:5509061 20170105 MGI 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20191107 MGI PMID:27229483 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20191107 MGI PMID:27229483 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20191107 MGI PMID:27229483 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20191107 MGI PMID:27229483 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0009922 increased transitional stage T1 B cell number IEA N RGD:5509061 20201231 MGI 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20200402 MGI 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20191107 MGI PMID:27229483 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20191107 MGI PMID:27229483 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0013797 abnormal ileal goblet cell morphology IAGP N RGD:5509061 20191107 MGI PMID:27229483 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20191107 MGI PMID:27229483 1551368 Arhgap17 Rho GTPase activating protein 17 gene MP:0014201 abnormal intestinal epithelium physiology IAGP N RGD:5509061 20191107 MGI PMID:27229483 1551369 Gtpbp6 GTP binding protein 6 (putative) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:15870284 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:15870284 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15870284 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15870284 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15870284 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:15870284 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15870284 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230601 MGI 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:15870284 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:15870284 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15870284 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0005314 absent thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:15870284 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0010017 visceral vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15870284 1551371 Abca5 ATP-binding cassette, sub-family A member 5 gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20161124 MGI PMID:15870284 1551372 Fgf12 fibroblast growth factor 12 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:17678857 1551372 Fgf12 fibroblast growth factor 12 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17678857 1551372 Fgf12 fibroblast growth factor 12 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17678857 1551372 Fgf12 fibroblast growth factor 12 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17678857 1551372 Fgf12 fibroblast growth factor 12 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:17678857 1551372 Fgf12 fibroblast growth factor 12 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200514 MGI 1551372 Fgf12 fibroblast growth factor 12 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17678857 1551372 Fgf12 fibroblast growth factor 12 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:17678857 1551372 Fgf12 fibroblast growth factor 12 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:17678857 1551372 Fgf12 fibroblast growth factor 12 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1551373 Fibp fibroblast growth factor (acidic) intracellular binding protein gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20221110 MGI 1551373 Fibp fibroblast growth factor (acidic) intracellular binding protein gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20221110 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200310 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0000601 small liver IEA N RGD:5509061 20200310 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0000692 small spleen IEA N RGD:5509061 20200310 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0000706 small thymus IEA N RGD:5509061 20200310 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0000774 decreased brain size IEA N RGD:5509061 20200310 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0002188 small heart IEA N RGD:5509061 20200310 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:29920190 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0002691 small stomach IEA N RGD:5509061 20200310 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0003641 small lung IEA N RGD:5509061 20200310 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20200310 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20211021 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20200310 MGI PMID:29920190 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20200310 MGI PMID:29920190 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20200310 MGI PMID:29920190 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20200310 MGI PMID:29920190 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:29920190 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200310 MGI 1551375 Hectd3 HECT domain E3 ubiquitin protein ligase 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200310 MGI 1551376 Alpk3 alpha-kinase 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0010545 abnormal heart layer morphology IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20210128 MGI 1551376 Alpk3 alpha-kinase 3 gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551376 Alpk3 alpha-kinase 3 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20200310 MGI PMID:21441111 1551376 Alpk3 alpha-kinase 3 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:21441111 1551377 Erlin1 ER lipid raft associated 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220519 MGI 1551377 Erlin1 ER lipid raft associated 1 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20220519 MGI 1551377 Erlin1 ER lipid raft associated 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 1551377 Erlin1 ER lipid raft associated 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1551377 Erlin1 ER lipid raft associated 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1551377 Erlin1 ER lipid raft associated 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20220519 MGI 1551377 Erlin1 ER lipid raft associated 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1551377 Erlin1 ER lipid raft associated 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1551377 Erlin1 ER lipid raft associated 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220519 MGI 1551377 Erlin1 ER lipid raft associated 1 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20220519 MGI 1551377 Erlin1 ER lipid raft associated 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1551377 Erlin1 ER lipid raft associated 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1551377 Erlin1 ER lipid raft associated 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1551379 Rap1gap Rap1 GTPase-activating protein gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1551379 Rap1gap Rap1 GTPase-activating protein gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1551379 Rap1gap Rap1 GTPase-activating protein gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1551379 Rap1gap Rap1 GTPase-activating protein gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1551379 Rap1gap Rap1 GTPase-activating protein gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1551380 Sypl2 synaptophysin like 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:10613905 1551380 Sypl2 synaptophysin like 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:10613905 1551380 Sypl2 synaptophysin like 2 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:10613905 1551380 Sypl2 synaptophysin like 2 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:10613905 1551380 Sypl2 synaptophysin like 2 gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20200310 MGI PMID:10613905 1551380 Sypl2 synaptophysin like 2 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20200310 MGI PMID:10613905 1551380 Sypl2 synaptophysin like 2 gene MP:0009411 abnormal skeletal muscle fiber triad morphology IAGP N RGD:5509061 20200310 MGI PMID:10613905 1551381 Esrrg estrogen-related receptor gamma gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:21138943 1551381 Esrrg estrogen-related receptor gamma gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:17618853 1551381 Esrrg estrogen-related receptor gamma gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:17618853 1551381 Esrrg estrogen-related receptor gamma gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:21138943 1551381 Esrrg estrogen-related receptor gamma gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20141003 MGI PMID:21138943 1551381 Esrrg estrogen-related receptor gamma gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:17618853 1551381 Esrrg estrogen-related receptor gamma gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:21138943 1551381 Esrrg estrogen-related receptor gamma gene MP:0005604 hyperekplexia IEA N RGD:5509061 20111116 MGI 1551381 Esrrg estrogen-related receptor gamma gene MP:0006325 impaired hearing IAGP N RGD:5509061 20150917 MGI PMID:23540940 1551381 Esrrg estrogen-related receptor gamma gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20150917 MGI PMID:23540940 1551381 Esrrg estrogen-related receptor gamma gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:17618853 1551381 Esrrg estrogen-related receptor gamma gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:17618853 1551381 Esrrg estrogen-related receptor gamma gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:17618853 1551381 Esrrg estrogen-related receptor gamma gene MP:0010570 prolonged ST segment IAGP N RGD:5509061 20141003 MGI PMID:17618853 1551381 Esrrg estrogen-related receptor gamma gene MP:0010636 bundle branch block IAGP N RGD:5509061 20141003 MGI PMID:17618853 1551381 Esrrg estrogen-related receptor gamma gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:17618853 1551381 Esrrg estrogen-related receptor gamma gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17618853 1551381 Esrrg estrogen-related receptor gamma gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19965931 1551381 Esrrg estrogen-related receptor gamma gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20150917 MGI PMID:23540940 1551381 Esrrg estrogen-related receptor gamma gene MP:0011303 absent kidney papilla IAGP N RGD:5509061 20141003 MGI PMID:21138943 1551381 Esrrg estrogen-related receptor gamma gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:17618853 1551381 Esrrg estrogen-related receptor gamma gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20150917 MGI PMID:23540940 1551381 Esrrg estrogen-related receptor gamma gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20150917 MGI PMID:23540940 1551381 Esrrg estrogen-related receptor gamma gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:17618853 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20160804 MGI 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20170824 MGI PMID:28248300 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20160922 MGI PMID:24652767 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0009611 epidermis stratum spinosum hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0010535 myocardium steatosis IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0011579 decreased lipoprotein lipase activity IAGP N RGD:5509061 20141003 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0011582 decreased triglyceride lipase activity IAGP N RGD:5509061 20141003 MGI PMID:20023287 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0011582 decreased triglyceride lipase activity IAGP N RGD:5509061 20141003 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20170824 MGI PMID:28248300 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:23733885 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0031418 increased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:23413028 1551382 Abhd5 abhydrolase domain containing 5 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:23413028 1551383 Ifi47 interferon gamma inducible protein 47 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:11457893 1551390 Usp36 ubiquitin specific peptidase 36 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:29273634 1551390 Usp36 ubiquitin specific peptidase 36 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20200310 MGI 1551390 Usp36 ubiquitin specific peptidase 36 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:29273634 1551390 Usp36 ubiquitin specific peptidase 36 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29273634 1551390 Usp36 ubiquitin specific peptidase 36 gene MP:0012129 failure of blastocyst formation IAGP N RGD:5509061 20200310 MGI PMID:29273634 1551390 Usp36 ubiquitin specific peptidase 36 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:29273634 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:11181567 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:11181567 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:11181567 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:11181567 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:11181567 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0000884 delaminated Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:11181567 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11181567 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11181567 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11181567 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:11181567 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11181567 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11181567 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0002608 increased hematocrit IAGP N RGD:6893636|PMID:18551038 20120913 RGD 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:11181567 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0005563 abnormal hemoglobin content IAGP N RGD:6893636|PMID:18551038 20120913 RGD 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20638879 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20180920 MGI PMID:11181567 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20180920 MGI PMID:19204075 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20180920 MGI PMID:20638879 1551392 Mthfr methylenetetrahydrofolate reductase gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:11181567 1551394 Pon2 paraoxonase 2 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16891303 1551394 Pon2 paraoxonase 2 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20210128 MGI 1551394 Pon2 paraoxonase 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16891303 1551394 Pon2 paraoxonase 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16891303 1551394 Pon2 paraoxonase 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:16891303 1551394 Pon2 paraoxonase 2 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16891303 1551394 Pon2 paraoxonase 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1551394 Pon2 paraoxonase 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16891303 1551394 Pon2 paraoxonase 2 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16891303 1551394 Pon2 paraoxonase 2 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16891303 1551394 Pon2 paraoxonase 2 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:16891303 1551394 Pon2 paraoxonase 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16891303 1551394 Pon2 paraoxonase 2 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:16891303 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20200310 MGI PMID:16715502 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:22689267 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20200310 MGI PMID:22689267 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200310 MGI PMID:22418434 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20200310 MGI PMID:16715502 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20200310 MGI PMID:22689267 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0003385 abnormal body wall morphology IAGP N RGD:5509061 20200310 MGI PMID:22689267 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:22689267 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:22689267 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:22418434 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:22418434 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20200310 MGI PMID:22689267 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:22689267 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0008797 facial cleft IAGP N RGD:5509061 20200310 MGI PMID:22689267 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20200310 MGI PMID:22418434 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16715502 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0012535 abnormal optic fissure closure IAGP N RGD:5509061 20200310 MGI PMID:22689267 1551398 Nuak1 NUAK family, SNF1-like kinase, 1 gene MP:0031617 abnormal skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:22418434 1551400 Jmjd1c jumonji domain containing 1C gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:24006281 1551400 Jmjd1c jumonji domain containing 1C gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:24006281 1551400 Jmjd1c jumonji domain containing 1C gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20200310 MGI 1551400 Jmjd1c jumonji domain containing 1C gene MP:0002546 mydriasis IEA N RGD:5509061 20200310 MGI 1551400 Jmjd1c jumonji domain containing 1C gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:24006281 1551400 Jmjd1c jumonji domain containing 1C gene MP:0003036 vertebral transformation IEA N RGD:5509061 20200310 MGI 1551400 Jmjd1c jumonji domain containing 1C gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:24006281 1551400 Jmjd1c jumonji domain containing 1C gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200310 MGI PMID:24006281 1551400 Jmjd1c jumonji domain containing 1C gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20200310 MGI PMID:24006281 1551400 Jmjd1c jumonji domain containing 1C gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20200310 MGI PMID:24006281 1551400 Jmjd1c jumonji domain containing 1C gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551400 Jmjd1c jumonji domain containing 1C gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:24006281 1551400 Jmjd1c jumonji domain containing 1C gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:24006281 1551401 Sec11c SEC11 homolog C, signal peptidase complex subunit gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1551403 Ndufs1 NADH:ubiquinone oxidoreductase core subunit S1 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 1551403 Ndufs1 NADH:ubiquinone oxidoreductase core subunit S1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1551403 Ndufs1 NADH:ubiquinone oxidoreductase core subunit S1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1551403 Ndufs1 NADH:ubiquinone oxidoreductase core subunit S1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20160421 MGI 1551403 Ndufs1 NADH:ubiquinone oxidoreductase core subunit S1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1551403 Ndufs1 NADH:ubiquinone oxidoreductase core subunit S1 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20170105 MGI 1551403 Ndufs1 NADH:ubiquinone oxidoreductase core subunit S1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1551403 Ndufs1 NADH:ubiquinone oxidoreductase core subunit S1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20201022 MGI 1551403 Ndufs1 NADH:ubiquinone oxidoreductase core subunit S1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1551403 Ndufs1 NADH:ubiquinone oxidoreductase core subunit S1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1551403 Ndufs1 NADH:ubiquinone oxidoreductase core subunit S1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551403 Ndufs1 NADH:ubiquinone oxidoreductase core subunit S1 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 1551403 Ndufs1 NADH:ubiquinone oxidoreductase core subunit S1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20240523 MGI 1551404 Wdr55 WD repeat domain 55 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15902260 1551405 Gpm6b glycoprotein m6b gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0010205 abnormal oligodendrocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0010749 absent visual evoked potential IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551405 Gpm6b glycoprotein m6b gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:23322581 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17589504 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20221215 MGI 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20221215 MGI 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0000897 abnormal midbrain morphology IEA N RGD:5509061 20221215 MGI 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17589504 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:17589504 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20220811 MGI 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20221215 MGI 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0002809 increased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:17589504 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:17589504 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20221215 MGI 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20221215 MGI 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:17589504 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0008797 facial cleft IEA N RGD:5509061 20221215 MGI 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17589504 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17589504 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20240523 MGI 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17589504 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0012705 increased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17589504 1551408 Ambra1 autophagy/beclin 1 regulator 1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:17589504 1551409 Bace2 beta-site APP-cleaving enzyme 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 1551409 Bace2 beta-site APP-cleaving enzyme 2 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20181108 MGI PMID:23754390 1551409 Bace2 beta-site APP-cleaving enzyme 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15987683 1551409 Bace2 beta-site APP-cleaving enzyme 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1551409 Bace2 beta-site APP-cleaving enzyme 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15987683 1551409 Bace2 beta-site APP-cleaving enzyme 2 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20181108 MGI PMID:23754390 1551409 Bace2 beta-site APP-cleaving enzyme 2 gene MP:0005077 abnormal melanogenesis IAGP N RGD:5509061 20181108 MGI PMID:23754390 1551409 Bace2 beta-site APP-cleaving enzyme 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:15987683 1551409 Bace2 beta-site APP-cleaving enzyme 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15987683 1551409 Bace2 beta-site APP-cleaving enzyme 2 gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20181108 MGI PMID:23754390 1551409 Bace2 beta-site APP-cleaving enzyme 2 gene MP:0010192 abnormal retina melanin granule morphology IAGP N RGD:5509061 20181108 MGI PMID:23754390 1551409 Bace2 beta-site APP-cleaving enzyme 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15987683 1551409 Bace2 beta-site APP-cleaving enzyme 2 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20210128 MGI 1551410 Exoc8 exocyst complex component 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170105 MGI 1551410 Exoc8 exocyst complex component 8 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551410 Exoc8 exocyst complex component 8 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:3875649 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15117762 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:2884254 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11104803 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:805203 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14634110 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:2884254 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:2884254 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15117762 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:8890160 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:11104803 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:14634110 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:9088978 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11449370 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11104803 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15331445 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:7552994 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:8890160 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9088978 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9371815 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:9088978 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:17574818 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15331445 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:2884254 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11104803 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15331445 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7552994 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8890160 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:11104803 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:11104803 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:3875649 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002403 abnormal pre-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14634110 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002403 abnormal pre-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:3875649 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15117762 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12618482 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:805203 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11104803 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14634110 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15331445 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:15117762 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:15117762 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002491 decreased IgD level IEA N RGD:5509061 20111116 MGI 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002493 increased IgG level IEA N RGD:5509061 20111116 MGI 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:2884254 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0002497 increased IgE level IEA N RGD:5509061 20111116 MGI 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11104803 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:2884254 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:15117762 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:9371815 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11104803 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:14634110 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:805203 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8890160 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9088978 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:15117762 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11104803 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12618482 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:805203 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9088978 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9371815 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:805203 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:12842985 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20141003 MGI 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:11371362 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:7552994 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:17105816 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008203 absent B-1a cells IAGP N RGD:5509061 20141003 MGI PMID:14634110 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008203 absent B-1a cells IAGP N RGD:5509061 20141003 MGI PMID:8890160 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15331445 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:7552994 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:8890160 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9088978 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9371815 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:8890160 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008214 increased immature B cell number IEA N RGD:5509061 20141003 MGI 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15331445 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:8890160 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:7552994 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008246 abnormal leukocyte morphology IEA N RGD:5509061 20111116 MGI 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:9088978 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:9088978 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:9088978 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:11104803 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9088978 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:9088978 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11104803 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:15331445 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:7552994 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:8890160 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9088978 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9371815 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:9088978 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008523 absent lymph node germinal center IAGP N RGD:5509061 20141003 MGI PMID:9088978 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:15117762 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14634110 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:2884254 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:805203 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:12842985 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17998386 1551411 Btk Bruton agammaglobulinemia tyrosine kinase gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:15331445 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20220616 MGI PMID:34130995 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0000798 abnormal frontal lobe morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20201022 MGI 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20220616 MGI PMID:34130995 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20230601 MGI 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20220616 MGI PMID:34130995 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220811 MGI 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20200310 MGI PMID:25698751 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0009084 blind uterus IEA N RGD:5509061 20210826 MGI 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20200310 MGI PMID:25698751 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20200310 MGI PMID:25698751 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210128 MGI 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20220616 MGI PMID:34130995 1551412 Chmp2b charged multivesicular body protein 2B gene MP:0012448 abnormal primary motor cortex morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20221215 MGI 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:20652258 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19815013 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0000829 dilated fourth ventricle IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15755804 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20652258 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0000921 demyelination IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17314202 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17428816 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001393 ataxia IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19815013 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:17428816 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:19815013 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17428816 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:20652258 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17428816 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20652258 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17428816 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:20652258 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20221215 MGI 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17314202 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20652258 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0001967 deafness IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:17428816 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0002090 abnormal vision IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20221215 MGI 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:17314202 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21551073 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:20652258 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:21551073 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0003213 decreased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:19815013 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:17428816 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:21551073 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21551073 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20221215 MGI 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17314202 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17428816 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20652258 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21551073 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:20652258 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21551073 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21551073 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0005405 axon degeneration IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21803037 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21551073 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:20652258 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:21551073 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20230615 MGI PMID:17428816 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141218 MGI PMID:24055366 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17314202 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:17314202 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0008259 abnormal optic disk morphology IAGP N RGD:5509061 20190411 MGI PMID:17314202 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:17314202 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:21551073 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:20652258 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19815013 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0010061 increased creatine level IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20141003 MGI PMID:21803037 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:21551073 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17314202 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21551073 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17428816 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20652258 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:21551073 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141218 MGI PMID:24055366 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:20652258 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20150611 MGI PMID:21551073 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220811 MGI 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20180802 MGI PMID:23250881 1551416 Opa1 OPA1, mitochondrial dynamin like GTPase gene MP:0014386 decreased muscle fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:23250881 1551418 Rnd3 Rho family GTPase 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1551418 Rnd3 Rho family GTPase 3 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:23630292 1551418 Rnd3 Rho family GTPase 3 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:23630292 1551418 Rnd3 Rho family GTPase 3 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23630292 1551418 Rnd3 Rho family GTPase 3 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0002200 abnormal brain ventricular system morphology IAGP N RGD:5509061 20141003 MGI PMID:23630292 1551418 Rnd3 Rho family GTPase 3 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0002958 cerebral aqueductal stenosis IAGP N RGD:5509061 20141003 MGI PMID:23630292 1551418 Rnd3 Rho family GTPase 3 gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0003358 abnormal hypaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0005356 positive geotaxis IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:23630292 1551418 Rnd3 Rho family GTPase 3 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20170105 MGI 1551418 Rnd3 Rho family GTPase 3 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:23630292 1551418 Rnd3 Rho family GTPase 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:23630292 1551418 Rnd3 Rho family GTPase 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20201022 MGI 1551418 Rnd3 Rho family GTPase 3 gene MP:0020865 delayed suckling reflex loss IAGP N RGD:5509061 20220922 MGI PMID:21552537 1551418 Rnd3 Rho family GTPase 3 gene MP:0021165 behavioral developmental delay IAGP N RGD:5509061 20220922 MGI PMID:21552537 1551421 Angel1 angel homolog 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20200310 MGI 1551421 Angel1 angel homolog 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20200310 MGI 1551421 Angel1 angel homolog 1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20200310 MGI 1551423 Rnf113a1 ring finger protein 113A1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20151112 MGI PMID:24064296 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12543979 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:12543979 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12543979 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12543979 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12543979 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:12543979 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12543979 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23870131 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23870131 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20150326 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0002188 small heart IAGP N RGD:5509061 20151112 MGI PMID:24064296 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20151112 MGI PMID:24064296 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12543979 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18263735 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18263735 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20151112 MGI PMID:24064296 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20151112 MGI PMID:24064296 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12543979 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20141003 MGI 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160804 MGI 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0005571 decreased lactate dehydrogenase level IEA N RGD:5509061 20160804 MGI 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20151112 MGI PMID:24064296 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0008891 decreased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18263735 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0009906 increased tongue size IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0010266 decreased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18263735 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0010366 increased adrenal cortical tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0010384 increased renal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20151112 MGI PMID:24064296 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20151112 MGI PMID:24064296 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0010561 absent coronary vessels IAGP N RGD:5509061 20151112 MGI PMID:24064296 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0010733 abnormal axon initial segment morphology IAGP N RGD:5509061 20141003 MGI PMID:22632975 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22632975 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12543979 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20151112 MGI PMID:24064296 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0011392 increased fetal cardiomyocyte apoptosis IAGP N RGD:5509061 20151112 MGI PMID:24064296 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20151112 MGI PMID:24064296 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0013309 adrenal gland cyst IAGP N RGD:5509061 20141120 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0013328 visceromegaly IAGP N RGD:5509061 20141204 MGI PMID:20739274 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0020135 abnormal heart ventricle wall thickness IAGP N RGD:5509061 20151112 MGI PMID:24064296 1551425 Sptbn1 spectrin beta, non-erythrocytic 1 gene MP:0031525 thin left ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:24064296 1551428 Iqcb1 IQ calmodulin-binding motif containing 1 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20220519 MGI 1551428 Iqcb1 IQ calmodulin-binding motif containing 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20230601 MGI 1551428 Iqcb1 IQ calmodulin-binding motif containing 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1551428 Iqcb1 IQ calmodulin-binding motif containing 1 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20220519 MGI 1551428 Iqcb1 IQ calmodulin-binding motif containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551428 Iqcb1 IQ calmodulin-binding motif containing 1 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20211021 MGI 1551429 Ccl11 C-C motif chemokine ligand 11 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:16210640 1551429 Ccl11 C-C motif chemokine ligand 11 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16210640 1551429 Ccl11 C-C motif chemokine ligand 11 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:17060636 1551429 Ccl11 C-C motif chemokine ligand 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9808585 1551429 Ccl11 C-C motif chemokine ligand 11 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17060636 1551429 Ccl11 C-C motif chemokine ligand 11 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9034156 1551429 Ccl11 C-C motif chemokine ligand 11 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20150402 MGI PMID:16210640 1551429 Ccl11 C-C motif chemokine ligand 11 gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:9034156 1551430 Skic8 SKI8 subunit of superkiller complex gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1551430 Skic8 SKI8 subunit of superkiller complex gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20240523 MGI 1551430 Skic8 SKI8 subunit of superkiller complex gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1551432 Oprm1 opioid receptor, mu 1 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:16505249 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:19221053 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20200310 MGI PMID:20503133 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200310 MGI PMID:22231481 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:8893006 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:9126934 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20200310 MGI PMID:14499482 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20200310 MGI PMID:10727705 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:9126934 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:9126934 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20200310 MGI PMID:12525693 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20200310 MGI PMID:10835636 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20200310 MGI PMID:8893006 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20200310 MGI PMID:9037090 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:21232580 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001980 abnormal chemically-elicited antinociception IAGP N RGD:5509061 20200310 MGI PMID:21957251 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20200310 MGI PMID:18207746 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20200310 MGI PMID:21957251 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20200310 MGI PMID:19273844 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20200310 MGI PMID:19528658 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20200310 MGI PMID:21232580 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20200310 MGI PMID:9126934 1551432 Oprm1 opioid receptor, mu 1 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20200310 MGI PMID:9555078 1551432 Oprm1 opioid receptor, mu 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:19221053 1551432 Oprm1 opioid receptor, mu 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:12525693 1551432 Oprm1 opioid receptor, mu 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20200310 MGI PMID:9126934 1551432 Oprm1 opioid receptor, mu 1 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20200310 MGI PMID:15926936 1551432 Oprm1 opioid receptor, mu 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:9126934 1551432 Oprm1 opioid receptor, mu 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:9126934 1551432 Oprm1 opioid receptor, mu 1 gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20200310 MGI PMID:15355329 1551432 Oprm1 opioid receptor, mu 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20200310 MGI PMID:10727705 1551432 Oprm1 opioid receptor, mu 1 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:19221053 1551432 Oprm1 opioid receptor, mu 1 gene MP:0003063 increased coping response IAGP N RGD:5509061 20200310 MGI PMID:10835636 1551432 Oprm1 opioid receptor, mu 1 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20200310 MGI PMID:9126934 1551432 Oprm1 opioid receptor, mu 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20200310 MGI PMID:15893889 1551432 Oprm1 opioid receptor, mu 1 gene MP:0003959 abnormal lean body mass IAGP N RGD:5509061 20200310 MGI PMID:19221053 1551432 Oprm1 opioid receptor, mu 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:10515257 1551432 Oprm1 opioid receptor, mu 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:19528658 1551432 Oprm1 opioid receptor, mu 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:9037090 1551432 Oprm1 opioid receptor, mu 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:19221053 1551432 Oprm1 opioid receptor, mu 1 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20200310 MGI PMID:19221053 1551432 Oprm1 opioid receptor, mu 1 gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20200310 MGI PMID:19273844 1551432 Oprm1 opioid receptor, mu 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20200310 MGI PMID:9126934 1551432 Oprm1 opioid receptor, mu 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:17544222 1551432 Oprm1 opioid receptor, mu 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:11377918 1551432 Oprm1 opioid receptor, mu 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:21232580 1551432 Oprm1 opioid receptor, mu 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:24069332 1551432 Oprm1 opioid receptor, mu 1 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:15355329 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20200310 MGI PMID:19221053 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20200310 MGI PMID:19221053 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20200310 MGI PMID:9126934 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:9126934 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20200310 MGI PMID:19528658 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009713 enhanced conditioned place preference behavior IAGP N RGD:5509061 20200310 MGI PMID:11377918 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20200310 MGI PMID:18207746 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20200310 MGI PMID:24069332 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20200310 MGI PMID:15355329 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009753 enhanced behavioral response to morphine IAGP N RGD:5509061 20200310 MGI PMID:21957251 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20200310 MGI PMID:12781916 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20200310 MGI PMID:10195199 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20200310 MGI PMID:10515257 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20200310 MGI PMID:11032994 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20200310 MGI PMID:11377918 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20200310 MGI PMID:12781916 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20200310 MGI PMID:17544222 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20200310 MGI PMID:19528658 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20200310 MGI PMID:21232580 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20200310 MGI PMID:24069332 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20200310 MGI PMID:8893006 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20200310 MGI PMID:9126934 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20200310 MGI PMID:9555078 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:11377918 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:9555078 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009776 decreased behavioral withdrawal response IAGP N RGD:5509061 20200310 MGI PMID:10835636 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009778 impaired behavioral response to anesthetic IAGP N RGD:5509061 20200310 MGI PMID:10195199 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009778 impaired behavioral response to anesthetic IAGP N RGD:5509061 20200310 MGI PMID:11032994 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009778 impaired behavioral response to anesthetic IAGP N RGD:5509061 20200310 MGI PMID:17544222 1551432 Oprm1 opioid receptor, mu 1 gene MP:0009779 enhanced behavioral response to anesthetic IAGP N RGD:5509061 20200310 MGI PMID:11032994 1551432 Oprm1 opioid receptor, mu 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:19221053 1551432 Oprm1 opioid receptor, mu 1 gene MP:0030982 abnormal copulatory plug deposition IAGP N RGD:5509061 20240718 MGI PMID:9126934 1551432 Oprm1 opioid receptor, mu 1 gene MP:0031436 decreased copulatory plug deposition IAGP N RGD:5509061 20240718 MGI PMID:9126934 1551432 Oprm1 opioid receptor, mu 1 gene MP:0031628 abnormal intromission IAGP N RGD:5509061 20240718 MGI PMID:9126934 1551432 Oprm1 opioid receptor, mu 1 gene MP:0031650 decreased mounting behavior IAGP N RGD:5509061 20240905 MGI PMID:9126934 1551433 Ntn3 netrin 3 gene MP:0003177 allodynia IAGP N RGD:5509061 20230921 MGI PMID:36587114 1551433 Ntn3 netrin 3 gene MP:0014488 abnormal skin sensory neuron innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:36587114 1551433 Ntn3 netrin 3 gene MP:0020954 decreased mechanical nociceptive threshold IAGP N RGD:5509061 20230921 MGI PMID:36587114 1551436 Rbm8a RNA binding motif protein 8a gene MP:0000433 microcephaly IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0000433 microcephaly IAGP N RGD:5509061 20200310 MGI PMID:27618312 1551436 Rbm8a RNA binding motif protein 8a gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20200310 MGI PMID:27618312 1551436 Rbm8a RNA binding motif protein 8a gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0008947 increased neuron number IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20200310 MGI PMID:27618312 1551436 Rbm8a RNA binding motif protein 8a gene MP:0011724 ectopic cortical neuron IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0012504 increased forebrain apoptosis IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0013227 small brain ventricles IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0020069 decreased neocortex size IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0020388 decreased radial glial cell number IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0020392 abnormal radial glial cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551436 Rbm8a RNA binding motif protein 8a gene MP:0020393 increased neuronal precursor proliferation IAGP N RGD:5509061 20200310 MGI PMID:25948253 1551437 Wfikkn2 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20200310 MGI PMID:24019467 1551437 Wfikkn2 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 gene MP:0000480 increased rib number IAGP N RGD:5509061 20200310 MGI PMID:24019467 1551437 Wfikkn2 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:24019467 1551437 Wfikkn2 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:24019467 1551437 Wfikkn2 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 gene MP:0004650 increased lumbar vertebrae number IAGP N RGD:5509061 20200310 MGI PMID:24019467 1551437 Wfikkn2 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 gene MP:0004651 increased thoracic vertebrae number IAGP N RGD:5509061 20200310 MGI PMID:24019467 1551437 Wfikkn2 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20200310 MGI PMID:24019467 1551437 Wfikkn2 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20200310 MGI PMID:24019467 1551437 Wfikkn2 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20200310 MGI PMID:24019467 1551437 Wfikkn2 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20200310 MGI PMID:24019467 1551437 Wfikkn2 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20200310 MGI PMID:24019467 1551437 Wfikkn2 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 gene MP:0021206 abnormal limb muscle morphology IAGP N RGD:5509061 20221201 MGI PMID:24019467 1551442 Zhx2 zinc fingers and homeoboxes 2 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:67170 1551444 Rbm34 RNA binding motif protein 34 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1551445 Rnase11 ribonuclease, RNase A family, 11 (non-active) gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1551445 Rnase11 ribonuclease, RNase A family, 11 (non-active) gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1551445 Rnase11 ribonuclease, RNase A family, 11 (non-active) gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1551445 Rnase11 ribonuclease, RNase A family, 11 (non-active) gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1551445 Rnase11 ribonuclease, RNase A family, 11 (non-active) gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1551445 Rnase11 ribonuclease, RNase A family, 11 (non-active) gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1551445 Rnase11 ribonuclease, RNase A family, 11 (non-active) gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1551445 Rnase11 ribonuclease, RNase A family, 11 (non-active) gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1551445 Rnase11 ribonuclease, RNase A family, 11 (non-active) gene MP:0003918 decreased kidney weight IEA N RGD:5509061 20210826 MGI 1551445 Rnase11 ribonuclease, RNase A family, 11 (non-active) gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1551445 Rnase11 ribonuclease, RNase A family, 11 (non-active) gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20210520 MGI 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:15003629 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20200310 MGI PMID:16397237 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:16397237 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20200310 MGI PMID:11696558 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:16397237 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:16397237 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:29180569 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:16397237 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:16397237 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0003334 pancreas fibrosis IAGP N RGD:5509061 20200310 MGI PMID:11696558 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0003335 exocrine pancreatic insufficiency IAGP N RGD:5509061 20200310 MGI PMID:11696558 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15003629 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0005150 cachexia IAGP N RGD:5509061 20200310 MGI PMID:16397237 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20200310 MGI PMID:11696558 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20200310 MGI PMID:16397237 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20200310 MGI PMID:16645041 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20200310 MGI PMID:22510200 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0008780 increased pancreatic acinar cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:16397237 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0009043 increased pancreas adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:16397237 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20200310 MGI PMID:11696558 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20200310 MGI PMID:12829745 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20200310 MGI PMID:22510200 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0009147 abnormal pancreatic acinar cell physiology IAGP N RGD:5509061 20200310 MGI PMID:22510200 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20200310 MGI PMID:19028870 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0009155 pancreatic acinar hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:16397237 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0009160 abnormal pancreatic acinar cell zymogen granule morphology IAGP N RGD:5509061 20200310 MGI PMID:11696558 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0009160 abnormal pancreatic acinar cell zymogen granule morphology IAGP N RGD:5509061 20200310 MGI PMID:15003629 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0009160 abnormal pancreatic acinar cell zymogen granule morphology IAGP N RGD:5509061 20200310 MGI PMID:22510200 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20200310 MGI PMID:16645041 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0010172 abnormal mammary gland epithelium physiology IAGP N RGD:5509061 20200310 MGI PMID:16645041 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20200310 MGI PMID:16397237 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0013317 abnormal seminal vesicle development IAGP N RGD:5509061 20200310 MGI PMID:17901072 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0013594 abnormal parotid gland acinus morphology IAGP N RGD:5509061 20200310 MGI PMID:15003629 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0013781 abnormal mammary gland luminal epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:16645041 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0013899 abnormal seminal vesicle epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:17901072 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0013900 seminal vesicle epithelium degeneration IAGP N RGD:5509061 20200310 MGI PMID:17901072 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0013903 abnormal seminal vesicle fluid composition IAGP N RGD:5509061 20200310 MGI PMID:17901072 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0014098 decreased pancreatic amylase secretion IAGP N RGD:5509061 20200310 MGI PMID:22510200 1551446 Bhlha15 basic helix-loop-helix family, member a15 gene MP:0014126 increased mammary gland apoptosis IAGP N RGD:5509061 20200310 MGI PMID:16645041 1551450 Jam3 junction adhesion molecule 3 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20200220 MGI PMID:19109565 1551450 Jam3 junction adhesion molecule 3 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20200220 MGI PMID:19109565 1551450 Jam3 junction adhesion molecule 3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:17455169 1551450 Jam3 junction adhesion molecule 3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20200220 MGI PMID:19109565 1551450 Jam3 junction adhesion molecule 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20210826 MGI 1551450 Jam3 junction adhesion molecule 3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0000917 obstructive hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15372036 1551450 Jam3 junction adhesion molecule 3 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21147852 1551450 Jam3 junction adhesion molecule 3 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15372036 1551450 Jam3 junction adhesion molecule 3 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21147852 1551450 Jam3 junction adhesion molecule 3 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:21593193 1551450 Jam3 junction adhesion molecule 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200220 MGI PMID:19533782 1551450 Jam3 junction adhesion molecule 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20200220 MGI PMID:19109565 1551450 Jam3 junction adhesion molecule 3 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17455169 1551450 Jam3 junction adhesion molecule 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200220 MGI PMID:19533782 1551450 Jam3 junction adhesion molecule 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17455169 1551450 Jam3 junction adhesion molecule 3 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15372036 1551450 Jam3 junction adhesion molecule 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17455169 1551450 Jam3 junction adhesion molecule 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21593193 1551450 Jam3 junction adhesion molecule 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20200220 MGI PMID:19109565 1551450 Jam3 junction adhesion molecule 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15372036 1551450 Jam3 junction adhesion molecule 3 gene MP:0002083 premature death IAGP N RGD:5509061 20200220 MGI PMID:19533782 1551450 Jam3 junction adhesion molecule 3 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:17455169 1551450 Jam3 junction adhesion molecule 3 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15372036 1551450 Jam3 junction adhesion molecule 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17455169 1551450 Jam3 junction adhesion molecule 3 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15372036 1551450 Jam3 junction adhesion molecule 3 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20200220 MGI PMID:19109565 1551450 Jam3 junction adhesion molecule 3 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0004545 enlarged esophagus IAGP N RGD:5509061 20141003 MGI PMID:17455169 1551450 Jam3 junction adhesion molecule 3 gene MP:0004545 enlarged esophagus IAGP N RGD:5509061 20200220 MGI PMID:19109565 1551450 Jam3 junction adhesion molecule 3 gene MP:0004545 enlarged esophagus IAGP N RGD:5509061 20200220 MGI PMID:19533782 1551450 Jam3 junction adhesion molecule 3 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:21147852 1551450 Jam3 junction adhesion molecule 3 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20200220 MGI PMID:19533782 1551450 Jam3 junction adhesion molecule 3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200220 MGI PMID:19109565 1551450 Jam3 junction adhesion molecule 3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200220 MGI PMID:19533782 1551450 Jam3 junction adhesion molecule 3 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:21147852 1551450 Jam3 junction adhesion molecule 3 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20141003 MGI PMID:21147852 1551450 Jam3 junction adhesion molecule 3 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17455169 1551450 Jam3 junction adhesion molecule 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200220 MGI PMID:19109565 1551450 Jam3 junction adhesion molecule 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21593193 1551450 Jam3 junction adhesion molecule 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21593193 1551450 Jam3 junction adhesion molecule 3 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20220811 MGI 1551450 Jam3 junction adhesion molecule 3 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1551450 Jam3 junction adhesion molecule 3 gene MP:0013891 increased common myeloid progenitor cell number IAGP N RGD:5509061 20200220 MGI PMID:19109565 1551450 Jam3 junction adhesion molecule 3 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:21147852 1551450 Jam3 junction adhesion molecule 3 gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:23029139 1551450 Jam3 junction adhesion molecule 3 gene MP:0031109 subarachnoid hemorrhage IAGP N RGD:5509061 20200910 MGI PMID:23029139 1551451 Arl5a ADP-ribosylation factor-like 5A gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1551451 Arl5a ADP-ribosylation factor-like 5A gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1551453 Tbc1d22a TBC1 domain family, member 22a gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20210128 MGI 1551453 Tbc1d22a TBC1 domain family, member 22a gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 1551453 Tbc1d22a TBC1 domain family, member 22a gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20200310 MGI 1551453 Tbc1d22a TBC1 domain family, member 22a gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20210128 MGI 1551453 Tbc1d22a TBC1 domain family, member 22a gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1551453 Tbc1d22a TBC1 domain family, member 22a gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210128 MGI 1551453 Tbc1d22a TBC1 domain family, member 22a gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20210128 MGI 1551453 Tbc1d22a TBC1 domain family, member 22a gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1551453 Tbc1d22a TBC1 domain family, member 22a gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20200310 MGI 1551453 Tbc1d22a TBC1 domain family, member 22a gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20200310 MGI 1551453 Tbc1d22a TBC1 domain family, member 22a gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1551454 Plbd2 phospholipase B domain containing 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1551454 Plbd2 phospholipase B domain containing 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 1551455 Vkorc1l1 vitamin K epoxide reductase complex, subunit 1-like 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1551455 Vkorc1l1 vitamin K epoxide reductase complex, subunit 1-like 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1551455 Vkorc1l1 vitamin K epoxide reductase complex, subunit 1-like 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1551455 Vkorc1l1 vitamin K epoxide reductase complex, subunit 1-like 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1551455 Vkorc1l1 vitamin K epoxide reductase complex, subunit 1-like 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1551455 Vkorc1l1 vitamin K epoxide reductase complex, subunit 1-like 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1551455 Vkorc1l1 vitamin K epoxide reductase complex, subunit 1-like 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220811 MGI 1551455 Vkorc1l1 vitamin K epoxide reductase complex, subunit 1-like 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1551455 Vkorc1l1 vitamin K epoxide reductase complex, subunit 1-like 1 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20220811 MGI 1551455 Vkorc1l1 vitamin K epoxide reductase complex, subunit 1-like 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1551455 Vkorc1l1 vitamin K epoxide reductase complex, subunit 1-like 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1551455 Vkorc1l1 vitamin K epoxide reductase complex, subunit 1-like 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1551455 Vkorc1l1 vitamin K epoxide reductase complex, subunit 1-like 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1551455 Vkorc1l1 vitamin K epoxide reductase complex, subunit 1-like 1 gene MP:0011922 abnormal circulating osteocalcin level IAGP N RGD:5509061 20181004 MGI PMID:25753038 1551455 Vkorc1l1 vitamin K epoxide reductase complex, subunit 1-like 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0002083 premature death IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0002766 situs inversus IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551456 Zmynd10 zinc finger, MYND domain containing 10 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20180712 MGI PMID:29601588 1551459 Nbeal2 neurobeachin-like 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200310 MGI 1551459 Nbeal2 neurobeachin-like 2 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20200310 MGI 1551459 Nbeal2 neurobeachin-like 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:26950939 1551459 Nbeal2 neurobeachin-like 2 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20200310 MGI PMID:25258341 1551459 Nbeal2 neurobeachin-like 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:23863626 1551459 Nbeal2 neurobeachin-like 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:25258341 1551459 Nbeal2 neurobeachin-like 2 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:25258341 1551459 Nbeal2 neurobeachin-like 2 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20200310 MGI PMID:23863626 1551459 Nbeal2 neurobeachin-like 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:25258341 1551459 Nbeal2 neurobeachin-like 2 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:23863626 1551459 Nbeal2 neurobeachin-like 2 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:25258341 1551459 Nbeal2 neurobeachin-like 2 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20200310 MGI PMID:25258341 1551459 Nbeal2 neurobeachin-like 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200310 MGI PMID:23863626 1551459 Nbeal2 neurobeachin-like 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200310 MGI PMID:25258341 1551459 Nbeal2 neurobeachin-like 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200310 MGI PMID:26950939 1551459 Nbeal2 neurobeachin-like 2 gene MP:0003405 abnormal platelet shape IAGP N RGD:5509061 20200310 MGI PMID:25258341 1551459 Nbeal2 neurobeachin-like 2 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20200310 MGI PMID:23863626 1551459 Nbeal2 neurobeachin-like 2 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20200310 MGI PMID:25258341 1551459 Nbeal2 neurobeachin-like 2 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20200310 MGI PMID:23863626 1551459 Nbeal2 neurobeachin-like 2 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20200310 MGI PMID:23863626 1551459 Nbeal2 neurobeachin-like 2 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20200310 MGI PMID:23863626 1551459 Nbeal2 neurobeachin-like 2 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20200310 MGI PMID:23863626 1551459 Nbeal2 neurobeachin-like 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:23863626 1551459 Nbeal2 neurobeachin-like 2 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20200310 MGI PMID:23863626 1551459 Nbeal2 neurobeachin-like 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1551459 Nbeal2 neurobeachin-like 2 gene MP:0011747 myelofibrosis IAGP N RGD:5509061 20200310 MGI PMID:25258341 1551459 Nbeal2 neurobeachin-like 2 gene MP:0012197 impaired myofibroblast differentiation IAGP N RGD:5509061 20200310 MGI PMID:23863626 1551459 Nbeal2 neurobeachin-like 2 gene MP:0020399 enhanced megakaryocyte emperipolesis IAGP N RGD:5509061 20200310 MGI PMID:23863626 1551459 Nbeal2 neurobeachin-like 2 gene MP:0020399 enhanced megakaryocyte emperipolesis IAGP N RGD:5509061 20200310 MGI PMID:26950939 1551459 Nbeal2 neurobeachin-like 2 gene MP:0020431 decreased platelet alpha-granule number IAGP N RGD:5509061 20200310 MGI PMID:23863626 1551459 Nbeal2 neurobeachin-like 2 gene MP:0020431 decreased platelet alpha-granule number IAGP N RGD:5509061 20200310 MGI PMID:25258341 1551459 Nbeal2 neurobeachin-like 2 gene MP:0020431 decreased platelet alpha-granule number IAGP N RGD:5509061 20200310 MGI PMID:26950939 1551459 Nbeal2 neurobeachin-like 2 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201001 MGI PMID:23863626 1551460 Mkrn1 makorin, ring finger protein, 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16882727 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0000416 sparse hair IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20200310 MGI PMID:16075059 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:16075058 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:21748766 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20200310 MGI PMID:21748766 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20200310 MGI PMID:16075058 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20200310 MGI PMID:16075059 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20200310 MGI PMID:21748766 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0005638 hemochromatosis IAGP N RGD:5509061 20200310 MGI PMID:16075058 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0005638 hemochromatosis IAGP N RGD:5509061 20200310 MGI PMID:16075059 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0005638 hemochromatosis IAGP N RGD:5509061 20200310 MGI PMID:21748766 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20200310 MGI PMID:16075058 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20200310 MGI PMID:16075059 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20200310 MGI PMID:21748766 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20200310 MGI PMID:16075058 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20200310 MGI PMID:16075059 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20200310 MGI PMID:21748766 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20200310 MGI PMID:16075059 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20200310 MGI PMID:21748766 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20200310 MGI PMID:16075059 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20200310 MGI PMID:21748766 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0011897 decreased circulating unsaturated transferrin level IAGP N RGD:5509061 20200310 MGI PMID:21748766 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0013302 increased pancreas iron level IAGP N RGD:5509061 20200310 MGI PMID:16075058 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0013303 decreased pancreas iron level IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0020367 increased heart iron level IAGP N RGD:5509061 20200310 MGI PMID:16075058 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0020368 decreased heart iron level IAGP N RGD:5509061 20200310 MGI PMID:20200349 1551463 Hjv hemojuvelin BMP co-receptor gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220811 MGI 1551466 Arcn1 archain 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:12955145 1551466 Arcn1 archain 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:20502676 1551466 Arcn1 archain 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:20502676 1551466 Arcn1 archain 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20502676 1551466 Arcn1 archain 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:20502676 1551466 Arcn1 archain 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20502676 1551466 Arcn1 archain 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20502676 1551466 Arcn1 archain 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20502676 1551466 Arcn1 archain 1 gene MP:0003214 neurofibrillary tangles IAGP N RGD:5509061 20141003 MGI PMID:20502676 1551466 Arcn1 archain 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:12955145 1551466 Arcn1 archain 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:20502676 1551466 Arcn1 archain 1 gene MP:0008733 abnormal hair shaft melanin granule distribution IAGP N RGD:5509061 20141003 MGI PMID:20502676 1551466 Arcn1 archain 1 gene MP:0009992 abnormal cerebellum vermis lobule IX morphology IAGP N RGD:5509061 20141003 MGI PMID:20502676 1551466 Arcn1 archain 1 gene MP:0009994 abnormal cerebellum vermis lobule VI morphology IAGP N RGD:5509061 20141003 MGI PMID:20502676 1551466 Arcn1 archain 1 gene MP:0009995 abnormal cerebellum vermis lobule VII morphology IAGP N RGD:5509061 20141003 MGI PMID:20502676 1551466 Arcn1 archain 1 gene MP:0009997 abnormal cerebellum vermis lobule X morphology IAGP N RGD:5509061 20141003 MGI PMID:20502676 1551466 Arcn1 archain 1 gene MP:0030949 abnormal Golgi vesicle transport IAGP N RGD:5509061 20190725 MGI PMID:20502676 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:17761531 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:3410303 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:6322428 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0001513 limb grasping IEA N RGD:5509061 20230601 MGI 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17761531 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:6322428 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0002095 abnormal skin pigmentation IEA N RGD:5509061 20111116 MGI 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17090228 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:17384153 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0002877 abnormal melanocyte morphology IEA N RGD:5509061 20111116 MGI 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0003798 abnormal Harderian gland pigmentation IEA N RGD:5509061 20111116 MGI 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0004721 abnormal platelet dense granule morphology IAGP N RGD:5509061 20141003 MGI PMID:12070017 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:10859366 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:12070017 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:17062724 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:17384153 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11266473 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:11266472 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:11266473 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:17090228 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:10859366 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:12070017 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0008327 abnormal corticotroph morphology IAGP N RGD:5509061 20141003 MGI PMID:17761531 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20141003 MGI PMID:11228153 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0008790 abnormal NK cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:11266473 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0008791 decreased NK cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0008834 abnormal melanosome transport IAGP N RGD:5509061 20141003 MGI PMID:11228153 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20141003 MGI PMID:12070017 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20141003 MGI PMID:17384153 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20141003 MGI PMID:12070017 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:12070017 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:17384153 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0009557 decreased platelet ADP level IAGP N RGD:5509061 20141003 MGI PMID:12070017 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0010809 abnormal club cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21160031 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20141003 MGI PMID:21160031 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0010943 abnormal bronchus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21160031 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170720 MGI PMID:10859366 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170720 MGI PMID:12070017 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170720 MGI PMID:17384153 1551470 Rab27a RAB27A, member RAS oncogene family gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:23160464 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:23426945 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20200310 MGI PMID:23426945 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20230601 MGI 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:23426945 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0000601 small liver IAGP N RGD:5509061 20200310 MGI PMID:23426945 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0000603 pale liver IEA N RGD:5509061 20230601 MGI 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230119 MGI 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:23426945 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230119 MGI 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:21778431 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:23426945 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20200310 MGI PMID:23426945 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:23426945 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:23426945 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230119 MGI 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20230119 MGI 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0003717 pallor IAGP N RGD:5509061 20200310 MGI PMID:23426945 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20200310 MGI PMID:23426945 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20230119 MGI 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:23426945 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20200310 MGI PMID:21778431 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:23426945 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230119 MGI 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0010194 absent lymphatic vessels IAGP N RGD:5509061 20200310 MGI PMID:21778431 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0010194 absent lymphatic vessels IAGP N RGD:5509061 20200310 MGI PMID:23426945 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21778431 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1551471 Ccbe1 collagen and calcium binding EGF domains 1 gene MP:0011243 decreased fetal derived definitive erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:23426945 1551477 Sall3 spalt like transcription factor 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1551477 Sall3 spalt like transcription factor 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1551477 Sall3 spalt like transcription factor 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1551477 Sall3 spalt like transcription factor 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1551477 Sall3 spalt like transcription factor 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1551477 Sall3 spalt like transcription factor 3 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:15282310 1551477 Sall3 spalt like transcription factor 3 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:15282310 1551477 Sall3 spalt like transcription factor 3 gene MP:0000959 abnormal somatic sensory system morphology IAGP N RGD:5509061 20141003 MGI PMID:15282310 1551477 Sall3 spalt like transcription factor 3 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15282310 1551477 Sall3 spalt like transcription factor 3 gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15282310 1551477 Sall3 spalt like transcription factor 3 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 1551477 Sall3 spalt like transcription factor 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1551477 Sall3 spalt like transcription factor 3 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1551477 Sall3 spalt like transcription factor 3 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230601 MGI 1551477 Sall3 spalt like transcription factor 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1551477 Sall3 spalt like transcription factor 3 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:15282310 1551477 Sall3 spalt like transcription factor 3 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:15282310 1551477 Sall3 spalt like transcription factor 3 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:15282310 1551477 Sall3 spalt like transcription factor 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1551477 Sall3 spalt like transcription factor 3 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1551477 Sall3 spalt like transcription factor 3 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20230601 MGI 1551477 Sall3 spalt like transcription factor 3 gene MP:0003154 abnormal soft palate morphology IAGP N RGD:5509061 20141003 MGI PMID:15282310 1551477 Sall3 spalt like transcription factor 3 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20230601 MGI 1551477 Sall3 spalt like transcription factor 3 gene MP:0010371 abnormal epiglottis morphology IAGP N RGD:5509061 20141003 MGI PMID:15282310 1551477 Sall3 spalt like transcription factor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15282310 1551477 Sall3 spalt like transcription factor 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1551480 Rfc2 replication factor C (activator 1) 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551480 Rfc2 replication factor C (activator 1) 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551486 Map3k2 mitogen-activated protein kinase kinase kinase 2 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:12138187 1551486 Map3k2 mitogen-activated protein kinase kinase kinase 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23125215 1551486 Map3k2 mitogen-activated protein kinase kinase kinase 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:12138187 1551486 Map3k2 mitogen-activated protein kinase kinase kinase 2 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:23125215 1551486 Map3k2 mitogen-activated protein kinase kinase kinase 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12138187 1551487 Samsn1 SAM domain, SH3 domain and nuclear localization signals, 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19923443 1551487 Samsn1 SAM domain, SH3 domain and nuclear localization signals, 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:19923443 1551487 Samsn1 SAM domain, SH3 domain and nuclear localization signals, 1 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19923443 1551487 Samsn1 SAM domain, SH3 domain and nuclear localization signals, 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19923443 1551487 Samsn1 SAM domain, SH3 domain and nuclear localization signals, 1 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:19923443 1551487 Samsn1 SAM domain, SH3 domain and nuclear localization signals, 1 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:19923443 1551487 Samsn1 SAM domain, SH3 domain and nuclear localization signals, 1 gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:19923443 1551487 Samsn1 SAM domain, SH3 domain and nuclear localization signals, 1 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:19923443 1551487 Samsn1 SAM domain, SH3 domain and nuclear localization signals, 1 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:19923443 1551487 Samsn1 SAM domain, SH3 domain and nuclear localization signals, 1 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:19923443 1551487 Samsn1 SAM domain, SH3 domain and nuclear localization signals, 1 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19923443 1551490 Fndc7 fibronectin type III domain containing 7 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210520 MGI 1551490 Fndc7 fibronectin type III domain containing 7 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210520 MGI 1551490 Fndc7 fibronectin type III domain containing 7 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20221215 MGI 1551493 Ddx24 DEAD box helicase 24 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210128 MGI 1551493 Ddx24 DEAD box helicase 24 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 1551493 Ddx24 DEAD box helicase 24 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20201022 MGI 1551493 Ddx24 DEAD box helicase 24 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1551493 Ddx24 DEAD box helicase 24 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180315 MGI PMID:24204270 1551493 Ddx24 DEAD box helicase 24 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20180315 MGI PMID:24204270 1551493 Ddx24 DEAD box helicase 24 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551493 Ddx24 DEAD box helicase 24 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1551493 Ddx24 DEAD box helicase 24 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1551493 Ddx24 DEAD box helicase 24 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20180315 MGI PMID:24204270 1551493 Ddx24 DEAD box helicase 24 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20240523 MGI 1551494 Hsdl2 hydroxysteroid dehydrogenase like 2 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0000341 abnormal bile color IAGP N RGD:5509061 20141003 MGI PMID:12429862 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20150122 MGI PMID:23954234 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0001307 fused cornea and lens IEA N RGD:5509061 20201231 MGI 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160421 MGI 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20151224 MGI PMID:22473008 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0001860 liver inflammation IAGP N RGD:5509061 20150122 MGI PMID:23954234 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20150122 MGI PMID:23954234 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20210812 MGI PMID:32488095 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20210812 MGI PMID:32488095 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150101 MGI PMID:22134889 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:15546952 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20150122 MGI PMID:23954234 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20210812 MGI PMID:32488095 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:21881209 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0003674 oxidative stress IAGP N RGD:5509061 20150122 MGI PMID:23954234 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0004147 increased porphyrin level IAGP N RGD:5509061 20150122 MGI PMID:23954234 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20210812 MGI PMID:32488095 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20150122 MGI PMID:23954234 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:12429862 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20210812 MGI PMID:32488095 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20210812 MGI PMID:32488095 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20210812 MGI PMID:32488095 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0005653 phototoxicity IAGP N RGD:5509061 20141003 MGI PMID:12429862 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0005654 porphyria IAGP N RGD:5509061 20141003 MGI PMID:12429862 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20150122 MGI PMID:23954234 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20210812 MGI PMID:32488095 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0008055 increased urine osmolality IAGP N RGD:5509061 20210812 MGI PMID:32488095 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20151224 MGI PMID:22473008 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20210812 MGI PMID:32488095 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15546952 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20150122 MGI PMID:23954234 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0009810 increased urine uric acid level IAGP N RGD:5509061 20151224 MGI PMID:22473008 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20210812 MGI PMID:32488095 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20150122 MGI PMID:23954234 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20150122 MGI PMID:23954234 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20150122 MGI PMID:23954234 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20150122 MGI PMID:23954234 1551496 Abcg2 ATP binding cassette subfamily G member 2 (Junior blood group) gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:23954234 1551497 Kazn kazrin, periplakin interacting protein gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1551497 Kazn kazrin, periplakin interacting protein gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1551497 Kazn kazrin, periplakin interacting protein gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 1551497 Kazn kazrin, periplakin interacting protein gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1551499 Caskin1 CASK interacting protein 1 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 1551499 Caskin1 CASK interacting protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191107 MGI PMID:30359304 1551499 Caskin1 CASK interacting protein 1 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20191107 MGI PMID:30359304 1551499 Caskin1 CASK interacting protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1551499 Caskin1 CASK interacting protein 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20191107 MGI PMID:30359304 1551499 Caskin1 CASK interacting protein 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20210603 MGI PMID:31727973 1551499 Caskin1 CASK interacting protein 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20170105 MGI 1551499 Caskin1 CASK interacting protein 1 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20191107 MGI PMID:30359304 1551499 Caskin1 CASK interacting protein 1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170105 MGI 1551499 Caskin1 CASK interacting protein 1 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20191107 MGI PMID:30359304 1551499 Caskin1 CASK interacting protein 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20191107 MGI PMID:30359304 1551499 Caskin1 CASK interacting protein 1 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20191107 MGI PMID:30359304 1551499 Caskin1 CASK interacting protein 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20210603 MGI PMID:31727973 1551499 Caskin1 CASK interacting protein 1 gene MP:0003908 decreased stereotypic behavior IAGP N RGD:5509061 20191107 MGI PMID:30359304 1551499 Caskin1 CASK interacting protein 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20191107 MGI PMID:30359304 1551499 Caskin1 CASK interacting protein 1 gene MP:0005407 hyperalgesia IAGP N RGD:5509061 20191107 MGI PMID:30359304 1551499 Caskin1 CASK interacting protein 1 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20191107 MGI PMID:30359304 1551499 Caskin1 CASK interacting protein 1 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20191107 MGI PMID:30359304 1551499 Caskin1 CASK interacting protein 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1551499 Caskin1 CASK interacting protein 1 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20191107 MGI PMID:30359304 1551499 Caskin1 CASK interacting protein 1 gene MP:0009455 enhanced cued conditioning behavior IAGP N RGD:5509061 20191107 MGI PMID:30359304 1551499 Caskin1 CASK interacting protein 1 gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20220519 MGI 1551499 Caskin1 CASK interacting protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551499 Caskin1 CASK interacting protein 1 gene MP:0011625 cystolithiasis IEA N RGD:5509061 20170105 MGI 1551499 Caskin1 CASK interacting protein 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20210603 MGI PMID:31727973 1551499 Caskin1 CASK interacting protein 1 gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20210603 MGI PMID:31727973 1551499 Caskin1 CASK interacting protein 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:30359304 1551501 Gpr108 G protein-coupled receptor 108 gene MP:0002764 short tibia IEA N RGD:5509061 20200514 MGI 1551501 Gpr108 G protein-coupled receptor 108 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1551501 Gpr108 G protein-coupled receptor 108 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20190103 MGI PMID:30332431 1551501 Gpr108 G protein-coupled receptor 108 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20190103 MGI PMID:30332431 1551501 Gpr108 G protein-coupled receptor 108 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20190103 MGI PMID:30332431 1551501 Gpr108 G protein-coupled receptor 108 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20190103 MGI PMID:30332431 1551501 Gpr108 G protein-coupled receptor 108 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20190103 MGI PMID:30332431 1551501 Gpr108 G protein-coupled receptor 108 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20211021 MGI 1551502 Ppp1r10 protein phosphatase 1, regulatory subunit 10 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20111116 MGI 1551503 Hrnr hornerin gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20201022 MGI 1551504 Ak4 adenylate kinase 4 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20231207 MGI 1551504 Ak4 adenylate kinase 4 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20230601 MGI 1551504 Ak4 adenylate kinase 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1551504 Ak4 adenylate kinase 4 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20231207 MGI 1551504 Ak4 adenylate kinase 4 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20230601 MGI 1551504 Ak4 adenylate kinase 4 gene MP:0002581 abnormal ileum morphology IEA N RGD:5509061 20231207 MGI 1551504 Ak4 adenylate kinase 4 gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20231207 MGI 1551504 Ak4 adenylate kinase 4 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 1551504 Ak4 adenylate kinase 4 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230601 MGI 1551504 Ak4 adenylate kinase 4 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230601 MGI 1551505 Hhipl1 hedgehog interacting protein-like 1 gene MP:0002989 small kidney IEA N RGD:5509061 20160811 MGI 1551505 Hhipl1 hedgehog interacting protein-like 1 gene MP:0004357 long tibia IEA N RGD:5509061 20221215 MGI 1551505 Hhipl1 hedgehog interacting protein-like 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20201217 MGI PMID:31163988 1551505 Hhipl1 hedgehog interacting protein-like 1 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20201217 MGI PMID:31163988 1551505 Hhipl1 hedgehog interacting protein-like 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1551505 Hhipl1 hedgehog interacting protein-like 1 gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20201217 MGI PMID:31163988 1551505 Hhipl1 hedgehog interacting protein-like 1 gene MP:0031509 decreased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:31163988 1551507 Plod2 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20201022 MGI PMID:30905411 1551507 Plod2 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1551507 Plod2 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1551507 Plod2 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1551507 Plod2 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20201022 MGI PMID:30905411 1551507 Plod2 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1551507 Plod2 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20201231 MGI 1551507 Plod2 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20201022 MGI PMID:30905411 1551507 Plod2 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20201022 MGI PMID:30905411 1551507 Plod2 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20201022 MGI PMID:30905411 1551507 Plod2 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551507 Plod2 procollagen lysine, 2-oxoglutarate 5-dioxygenase 2 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20201022 MGI PMID:30905411 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20201029 MGI PMID:32242237 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20201029 MGI PMID:32242237 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20201029 MGI PMID:32242237 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20210506 MGI PMID:32265257 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20201029 MGI PMID:32242237 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20210506 MGI PMID:32265257 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20210506 MGI PMID:32265257 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20210506 MGI PMID:32265257 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20201029 MGI PMID:32242237 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20201029 MGI PMID:32242237 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20201029 MGI PMID:32242237 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0008455 abnormal retina rod cell inner segment morphology IAGP N RGD:5509061 20201029 MGI PMID:32242237 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20201029 MGI PMID:32242237 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20210506 MGI PMID:32265257 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20201029 MGI PMID:32242237 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20201029 MGI PMID:32242237 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0013258 abnormal extracellular matrix morphology IAGP N RGD:5509061 20201029 MGI PMID:32242237 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20201029 MGI PMID:32242237 1551510 Impg2 interphotoreceptor matrix proteoglycan 2 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20201029 MGI PMID:32242237 1551511 Ccn3 cellular communication network factor 3 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1551511 Ccn3 cellular communication network factor 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1551511 Ccn3 cellular communication network factor 3 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0000532 kidney vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1551511 Ccn3 cellular communication network factor 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1551511 Ccn3 cellular communication network factor 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1551511 Ccn3 cellular communication network factor 3 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1551511 Ccn3 cellular communication network factor 3 gene MP:0001268 barrel chest IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1551511 Ccn3 cellular communication network factor 3 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0001506 limp posture IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:19934377 1551511 Ccn3 cellular communication network factor 3 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:19934377 1551511 Ccn3 cellular communication network factor 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1551511 Ccn3 cellular communication network factor 3 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 1551511 Ccn3 cellular communication network factor 3 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0002952 ventricular cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210826 MGI 1551511 Ccn3 cellular communication network factor 3 gene MP:0003385 abnormal body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0003808 increased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:19934377 1551511 Ccn3 cellular communication network factor 3 gene MP:0004348 long femur IAGP N RGD:5509061 20141003 MGI PMID:19934377 1551511 Ccn3 cellular communication network factor 3 gene MP:0004695 increased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:20139355 1551511 Ccn3 cellular communication network factor 3 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:19934377 1551511 Ccn3 cellular communication network factor 3 gene MP:0005353 abnormal patella morphology IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:19934377 1551511 Ccn3 cellular communication network factor 3 gene MP:0006137 venoocclusion IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0008069 abnormal joint mobility IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19934377 1551511 Ccn3 cellular communication network factor 3 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:19934377 1551511 Ccn3 cellular communication network factor 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0008919 fused tarsal bones IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0009084 blind uterus IEA N RGD:5509061 20210520 MGI 1551511 Ccn3 cellular communication network factor 3 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:19934377 1551511 Ccn3 cellular communication network factor 3 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:19934377 1551511 Ccn3 cellular communication network factor 3 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0030796 hip dislocation IAGP N RGD:5509061 20181011 MGI PMID:18289368 1551511 Ccn3 cellular communication network factor 3 gene MP:0031510 increased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:20139355 1551513 Txndc12 thioredoxin domain containing 12 (endoplasmic reticulum) gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20200310 MGI 1551516 Cc2d1b coiled-coil and C2 domain containing 1B gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20200310 MGI 1551516 Cc2d1b coiled-coil and C2 domain containing 1B gene MP:0001262 decreased body weight IEA N RGD:5509061 20200310 MGI 1551516 Cc2d1b coiled-coil and C2 domain containing 1B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201015 MGI PMID:26720614 1551516 Cc2d1b coiled-coil and C2 domain containing 1B gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20200310 MGI 1551516 Cc2d1b coiled-coil and C2 domain containing 1B gene MP:0004924 abnormal behavior IEA N RGD:5509061 20200310 MGI 1551519 Prss27 serine protease 27 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20210128 MGI 1551519 Prss27 serine protease 27 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23447538 1551520 Keg1 kidney expressed gene 1 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20240523 MGI 1551520 Keg1 kidney expressed gene 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1551520 Keg1 kidney expressed gene 1 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1551520 Keg1 kidney expressed gene 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1551520 Keg1 kidney expressed gene 1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20220811 MGI 1551520 Keg1 kidney expressed gene 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1551523 Ddx39a DEAD box helicase 39a gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201022 MGI 1551523 Ddx39a DEAD box helicase 39a gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210520 MGI 1551523 Ddx39a DEAD box helicase 39a gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1551523 Ddx39a DEAD box helicase 39a gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 1551523 Ddx39a DEAD box helicase 39a gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20201022 MGI 1551523 Ddx39a DEAD box helicase 39a gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20201022 MGI 1551523 Ddx39a DEAD box helicase 39a gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1551523 Ddx39a DEAD box helicase 39a gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1551523 Ddx39a DEAD box helicase 39a gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551523 Ddx39a DEAD box helicase 39a gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20201022 MGI 1551524 Mterf2 mitochondrial transcription termination factor 2 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20200310 MGI PMID:19490905 1551524 Mterf2 mitochondrial transcription termination factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:19490905 1551524 Mterf2 mitochondrial transcription termination factor 2 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20200310 MGI PMID:19490905 1551524 Mterf2 mitochondrial transcription termination factor 2 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20200310 MGI PMID:19490905 1551524 Mterf2 mitochondrial transcription termination factor 2 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20200310 MGI PMID:19490905 1551524 Mterf2 mitochondrial transcription termination factor 2 gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20200310 MGI PMID:19490905 1551524 Mterf2 mitochondrial transcription termination factor 2 gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20200310 MGI PMID:19490905 1551524 Mterf2 mitochondrial transcription termination factor 2 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20200310 MGI PMID:19490905 1551524 Mterf2 mitochondrial transcription termination factor 2 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20200310 MGI PMID:19490905 1551524 Mterf2 mitochondrial transcription termination factor 2 gene MP:0014394 increased skeletal muscle fiber mitochondrial DNA content IAGP N RGD:5509061 20240328 MGI PMID:19490905 1551524 Mterf2 mitochondrial transcription termination factor 2 gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20200310 MGI PMID:19490905 1551526 Fads3 fatty acid desaturase 3 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1551526 Fads3 fatty acid desaturase 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1551526 Fads3 fatty acid desaturase 3 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20180607 MGI PMID:28838557 1551526 Fads3 fatty acid desaturase 3 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20180607 MGI PMID:28838557 1551526 Fads3 fatty acid desaturase 3 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20181227 MGI 1551526 Fads3 fatty acid desaturase 3 gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20180607 MGI PMID:28838557 1551526 Fads3 fatty acid desaturase 3 gene MP:0010360 decreased liver free fatty acids level IAGP N RGD:5509061 20180607 MGI PMID:28838557 1551528 Sap18 Sin3-associated polypeptide 18 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1551528 Sap18 Sin3-associated polypeptide 18 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551528 Sap18 Sin3-associated polypeptide 18 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551529 Phf19 PHD finger protein 19 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20211209 MGI PMID:32821835 1551529 Phf19 PHD finger protein 19 gene MP:0000480 increased rib number IAGP N RGD:5509061 20211209 MGI PMID:32821835 1551529 Phf19 PHD finger protein 19 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20211209 MGI PMID:32821835 1551529 Phf19 PHD finger protein 19 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210805 MGI 1551529 Phf19 PHD finger protein 19 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210805 MGI 1551529 Phf19 PHD finger protein 19 gene MP:0001147 small testis IEA N RGD:5509061 20210805 MGI 1551529 Phf19 PHD finger protein 19 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20211209 MGI PMID:32821835 1551529 Phf19 PHD finger protein 19 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210805 MGI 1551529 Phf19 PHD finger protein 19 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20211209 MGI PMID:32821835 1551529 Phf19 PHD finger protein 19 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210805 MGI 1551529 Phf19 PHD finger protein 19 gene MP:0009709 hydrometra IEA N RGD:5509061 20210805 MGI 1551529 Phf19 PHD finger protein 19 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20231207 MGI 1551529 Phf19 PHD finger protein 19 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20211209 MGI PMID:32821835 1551529 Phf19 PHD finger protein 19 gene MP:0011181 increased hematopoietic cell number IAGP N RGD:5509061 20211209 MGI PMID:32821835 1551529 Phf19 PHD finger protein 19 gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20211209 MGI PMID:32821835 1551529 Phf19 PHD finger protein 19 gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20211209 MGI PMID:32821835 1551530 Rchy1 ring finger and CHY zinc finger domain containing 1 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:21791603 1551532 Cd99l2 CD99 antigen-like 2 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20200310 MGI PMID:23293350 1551532 Cd99l2 CD99 antigen-like 2 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20200310 MGI PMID:23293350 1551533 Cd248 CD248 antigen, endosialin gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200310 MGI 1551533 Cd248 CD248 antigen, endosialin gene MP:0001258 decreased body length IEA N RGD:5509061 20210520 MGI 1551533 Cd248 CD248 antigen, endosialin gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20200310 MGI 1551533 Cd248 CD248 antigen, endosialin gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1551533 Cd248 CD248 antigen, endosialin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:21402174 1551533 Cd248 CD248 antigen, endosialin gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:16492758 1551534 Pdia4 protein disulfide isomerase associated 4 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20200402 MGI 1551534 Pdia4 protein disulfide isomerase associated 4 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20200310 MGI PMID:28576878 1551534 Pdia4 protein disulfide isomerase associated 4 gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20200310 MGI PMID:28576878 1551534 Pdia4 protein disulfide isomerase associated 4 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20200310 MGI PMID:28576878 1551534 Pdia4 protein disulfide isomerase associated 4 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 1551535 Atp5mg ATP synthase membrane subunit g gene MP:0000274 enlarged heart IEA N RGD:5509061 20230720 MGI 1551535 Atp5mg ATP synthase membrane subunit g gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230720 MGI 1551535 Atp5mg ATP synthase membrane subunit g gene MP:0001406 abnormal gait IEA N RGD:5509061 20230720 MGI 1551535 Atp5mg ATP synthase membrane subunit g gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20230720 MGI 1551535 Atp5mg ATP synthase membrane subunit g gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20230720 MGI 1551535 Atp5mg ATP synthase membrane subunit g gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20230720 MGI 1551535 Atp5mg ATP synthase membrane subunit g gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20230720 MGI 1551535 Atp5mg ATP synthase membrane subunit g gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230720 MGI 1551541 Plekhn1 pleckstrin homology domain containing, family N member 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20211028 MGI PMID:27616329 1551541 Plekhn1 pleckstrin homology domain containing, family N member 1 gene MP:0001261 obese IAGP N RGD:5509061 20211028 MGI PMID:27616329 1551541 Plekhn1 pleckstrin homology domain containing, family N member 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20211028 MGI PMID:27616329 1551541 Plekhn1 pleckstrin homology domain containing, family N member 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20211028 MGI PMID:27616329 1551541 Plekhn1 pleckstrin homology domain containing, family N member 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20211028 MGI PMID:27616329 1551541 Plekhn1 pleckstrin homology domain containing, family N member 1 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20211028 MGI PMID:27616329 1551541 Plekhn1 pleckstrin homology domain containing, family N member 1 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20211028 MGI PMID:27616329 1551541 Plekhn1 pleckstrin homology domain containing, family N member 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20211028 MGI PMID:27616329 1551541 Plekhn1 pleckstrin homology domain containing, family N member 1 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20211028 MGI PMID:27616329 1551542 Chd6 chromodomain helicase DNA binding protein 6 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1551542 Chd6 chromodomain helicase DNA binding protein 6 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1551542 Chd6 chromodomain helicase DNA binding protein 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20111866 1551542 Chd6 chromodomain helicase DNA binding protein 6 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1551542 Chd6 chromodomain helicase DNA binding protein 6 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:20111866 1551542 Chd6 chromodomain helicase DNA binding protein 6 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:20111866 1551542 Chd6 chromodomain helicase DNA binding protein 6 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 1551544 Kif6 kinesin family member 6 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1551544 Kif6 kinesin family member 6 gene MP:0000440 domed cranium IAGP N RGD:5509061 20190718 MGI PMID:30475797 1551544 Kif6 kinesin family member 6 gene MP:0000774 decreased brain size IEA N RGD:5509061 20230601 MGI 1551544 Kif6 kinesin family member 6 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20190718 MGI PMID:30475797 1551544 Kif6 kinesin family member 6 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20190718 MGI PMID:30475797 1551544 Kif6 kinesin family member 6 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 1551544 Kif6 kinesin family member 6 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1551544 Kif6 kinesin family member 6 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1551544 Kif6 kinesin family member 6 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190718 MGI PMID:30475797 1551544 Kif6 kinesin family member 6 gene MP:0001505 hunched posture IAGP N RGD:5509061 20190718 MGI PMID:30475797 1551544 Kif6 kinesin family member 6 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20190718 MGI PMID:30475797 1551544 Kif6 kinesin family member 6 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20190718 MGI PMID:30475797 1551544 Kif6 kinesin family member 6 gene MP:0001925 male infertility IEA N RGD:5509061 20230601 MGI 1551544 Kif6 kinesin family member 6 gene MP:0001926 female infertility IEA N RGD:5509061 20230601 MGI 1551544 Kif6 kinesin family member 6 gene MP:0002083 premature death IAGP N RGD:5509061 20190718 MGI PMID:30475797 1551544 Kif6 kinesin family member 6 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230601 MGI 1551544 Kif6 kinesin family member 6 gene MP:0002188 small heart IEA N RGD:5509061 20230601 MGI 1551544 Kif6 kinesin family member 6 gene MP:0005238 increased brain size IAGP N RGD:5509061 20190718 MGI PMID:30475797 1551544 Kif6 kinesin family member 6 gene MP:0009709 hydrometra IEA N RGD:5509061 20230601 MGI 1551544 Kif6 kinesin family member 6 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20190718 MGI PMID:30475797 1551546 Foxi2 forkhead box I2 gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20180215 MGI PMID:26550799 1551546 Foxi2 forkhead box I2 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20180215 MGI PMID:26550799 1551546 Foxi2 forkhead box I2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180215 MGI PMID:26550799 1551546 Foxi2 forkhead box I2 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20180215 MGI PMID:26550799 1551546 Foxi2 forkhead box I2 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20180215 MGI PMID:26550799 1551546 Foxi2 forkhead box I2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1551549 Angpt1 angiopoietin 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20200310 MGI PMID:21606590 1551549 Angpt1 angiopoietin 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20200310 MGI PMID:8980224 1551549 Angpt1 angiopoietin 1 gene MP:0000264 failure of vascular branching IAGP N RGD:5509061 20200310 MGI PMID:8980224 1551549 Angpt1 angiopoietin 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20200310 MGI PMID:21606590 1551549 Angpt1 angiopoietin 1 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20200310 MGI PMID:8980224 1551549 Angpt1 angiopoietin 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20200310 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:21606590 1551549 Angpt1 angiopoietin 1 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200310 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20200310 MGI PMID:24048525 1551549 Angpt1 angiopoietin 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:8980224 1551549 Angpt1 angiopoietin 1 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20200310 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20200310 MGI PMID:8980224 1551549 Angpt1 angiopoietin 1 gene MP:0004226 absent Schlemm's canal IAGP N RGD:5509061 20200310 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:21606590 1551549 Angpt1 angiopoietin 1 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20200310 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20200310 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0005257 abnormal intraocular pressure IAGP N RGD:5509061 20200310 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200310 MGI PMID:21606590 1551549 Angpt1 angiopoietin 1 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20230810 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20200310 MGI PMID:8980224 1551549 Angpt1 angiopoietin 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:8980224 1551549 Angpt1 angiopoietin 1 gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20200310 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20200310 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20200310 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200310 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200310 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0009274 buphthalmos IAGP N RGD:5509061 20200310 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:24048525 1551549 Angpt1 angiopoietin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21606590 1551549 Angpt1 angiopoietin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:8980224 1551549 Angpt1 angiopoietin 1 gene MP:0012049 increased susceptilbility to retina ischemic injury IAGP N RGD:5509061 20200310 MGI PMID:24048525 1551549 Angpt1 angiopoietin 1 gene MP:0012066 decreased astrocyte number IAGP N RGD:5509061 20200310 MGI PMID:24048525 1551549 Angpt1 angiopoietin 1 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20200310 MGI PMID:8980224 1551549 Angpt1 angiopoietin 1 gene MP:0031213 increased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:25202984 1551549 Angpt1 angiopoietin 1 gene MP:0031500 increased cornea size IAGP N RGD:5509061 20230810 MGI PMID:25202984 1551552 Adss2 adenylosuccinate synthase 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1551552 Adss2 adenylosuccinate synthase 2 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20231207 MGI 1551552 Adss2 adenylosuccinate synthase 2 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20231207 MGI 1551552 Adss2 adenylosuccinate synthase 2 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 1551552 Adss2 adenylosuccinate synthase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1551552 Adss2 adenylosuccinate synthase 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20231207 MGI 1551552 Adss2 adenylosuccinate synthase 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20231207 MGI 1551555 Ptgr2 prostaglandin reductase 2 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1551556 P4ha3 procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha polypeptide III gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20210128 MGI 1551556 P4ha3 procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha polypeptide III gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210128 MGI 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0009596 abnormal stratum corneum lipid matrix formation IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200310 MGI 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551559 Slurp1 secreted Ly6/Plaur domain containing 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20200310 MGI PMID:24499735 1551560 Hpcal4 hippocalcin-like 4 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20220811 MGI 1551560 Hpcal4 hippocalcin-like 4 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20200409 MGI PMID:32015563 1551560 Hpcal4 hippocalcin-like 4 gene MP:0005631 decreased lung weight IEA N RGD:5509061 20201022 MGI 1551562 Crbn cereblon gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20190314 MGI PMID:30064974 1551562 Crbn cereblon gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1551562 Crbn cereblon gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1551562 Crbn cereblon gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20190314 MGI PMID:30064974 1551562 Crbn cereblon gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210128 MGI 1551562 Crbn cereblon gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:23349485 1551562 Crbn cereblon gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:23349485 1551562 Crbn cereblon gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23349485 1551562 Crbn cereblon gene MP:0001293 anophthalmia IAGP N RGD:5509061 20190314 MGI PMID:30064974 1551562 Crbn cereblon gene MP:0001333 absent optic nerve IEA N RGD:5509061 20210128 MGI 1551562 Crbn cereblon gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20190718 MGI PMID:29459374 1551562 Crbn cereblon gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1551562 Crbn cereblon gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23349485 1551562 Crbn cereblon gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23349485 1551562 Crbn cereblon gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:23349485 1551562 Crbn cereblon gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20190314 MGI PMID:30064974 1551562 Crbn cereblon gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23349485 1551562 Crbn cereblon gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20190314 MGI PMID:30064974 1551562 Crbn cereblon gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20190314 MGI PMID:30064974 1551562 Crbn cereblon gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23349485 1551562 Crbn cereblon gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23349485 1551562 Crbn cereblon gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:23349485 1551562 Crbn cereblon gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23349485 1551562 Crbn cereblon gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20190718 MGI PMID:29459374 1551562 Crbn cereblon gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20190314 MGI PMID:30064974 1551562 Crbn cereblon gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20190314 MGI PMID:30064974 1551562 Crbn cereblon gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1551562 Crbn cereblon gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23349485 1551562 Crbn cereblon gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23349485 1551562 Crbn cereblon gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21995942 1551562 Crbn cereblon gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20190718 MGI PMID:29459374 1551562 Crbn cereblon gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20190718 MGI PMID:29459374 1551562 Crbn cereblon gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20190314 MGI PMID:30064974 1551562 Crbn cereblon gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20190718 MGI PMID:29459374 1551562 Crbn cereblon gene MP:0013660 abnormal bone marrow hematopoietic cell morphology IAGP N RGD:5509061 20190314 MGI PMID:30064974 1551562 Crbn cereblon gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20190314 MGI PMID:30064974 1551562 Crbn cereblon gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:23349485 1551563 Cand2 cullin associated and neddylation dissociated 2 (putative) gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200310 MGI 1551563 Cand2 cullin associated and neddylation dissociated 2 (putative) gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20211021 MGI 1551563 Cand2 cullin associated and neddylation dissociated 2 (putative) gene MP:0005478 decreased circulating thyroxine level IEA N RGD:5509061 20211021 MGI 1551563 Cand2 cullin associated and neddylation dissociated 2 (putative) gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1551563 Cand2 cullin associated and neddylation dissociated 2 (putative) gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1551567 Glud1 glutamate dehydrogenase 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:19015267 1551567 Glud1 glutamate dehydrogenase 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:19015267 1551567 Glud1 glutamate dehydrogenase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200310 MGI PMID:19015267 1551567 Glud1 glutamate dehydrogenase 1 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20200310 MGI PMID:19015267 1551568 Pigv phosphatidylinositol glycan anchor biosynthesis, class V gene MP:0000111 cleft palate IEA N RGD:5509061 20200310 MGI 1551568 Pigv phosphatidylinositol glycan anchor biosynthesis, class V gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20200310 MGI 1551568 Pigv phosphatidylinositol glycan anchor biosynthesis, class V gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20200310 MGI 1551568 Pigv phosphatidylinositol glycan anchor biosynthesis, class V gene MP:0000519 hydronephrosis IEA N RGD:5509061 20200310 MGI 1551568 Pigv phosphatidylinositol glycan anchor biosynthesis, class V gene MP:0001265 decreased body size IEA N RGD:5509061 20200310 MGI 1551568 Pigv phosphatidylinositol glycan anchor biosynthesis, class V gene MP:0001297 microphthalmia IEA N RGD:5509061 20200310 MGI 1551568 Pigv phosphatidylinositol glycan anchor biosynthesis, class V gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20200310 MGI 1551568 Pigv phosphatidylinositol glycan anchor biosynthesis, class V gene MP:0002639 micrognathia IEA N RGD:5509061 20200310 MGI 1551568 Pigv phosphatidylinositol glycan anchor biosynthesis, class V gene MP:0003675 kidney cyst IEA N RGD:5509061 20200310 MGI 1551568 Pigv phosphatidylinositol glycan anchor biosynthesis, class V gene MP:0004158 right aortic arch IEA N RGD:5509061 20200310 MGI 1551568 Pigv phosphatidylinositol glycan anchor biosynthesis, class V gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20200310 MGI 1551568 Pigv phosphatidylinositol glycan anchor biosynthesis, class V gene MP:0010466 vascular ring IEA N RGD:5509061 20200310 MGI 1551568 Pigv phosphatidylinositol glycan anchor biosynthesis, class V gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20200310 MGI 1551569 Pcyt1b phosphate cytidylyltransferase 1, choline, beta isoform gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:15143167 1551569 Pcyt1b phosphate cytidylyltransferase 1, choline, beta isoform gene MP:0001128 ovary hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15143167 1551569 Pcyt1b phosphate cytidylyltransferase 1, choline, beta isoform gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:15143167 1551569 Pcyt1b phosphate cytidylyltransferase 1, choline, beta isoform gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:15143167 1551569 Pcyt1b phosphate cytidylyltransferase 1, choline, beta isoform gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15143167 1551569 Pcyt1b phosphate cytidylyltransferase 1, choline, beta isoform gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15143167 1551569 Pcyt1b phosphate cytidylyltransferase 1, choline, beta isoform gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:15143167 1551569 Pcyt1b phosphate cytidylyltransferase 1, choline, beta isoform gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15143167 1551569 Pcyt1b phosphate cytidylyltransferase 1, choline, beta isoform gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15143167 1551569 Pcyt1b phosphate cytidylyltransferase 1, choline, beta isoform gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15143167 1551569 Pcyt1b phosphate cytidylyltransferase 1, choline, beta isoform gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:15143167 1551569 Pcyt1b phosphate cytidylyltransferase 1, choline, beta isoform gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:15143167 1551573 Ascc1 activating signal cointegrator 1 complex subunit 1 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20220519 MGI 1551573 Ascc1 activating signal cointegrator 1 complex subunit 1 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20200402 MGI 1551573 Ascc1 activating signal cointegrator 1 complex subunit 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551573 Ascc1 activating signal cointegrator 1 complex subunit 1 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20220811 MGI 1551580 Gcsh glycine cleavage system protein H (aminomethyl carrier) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20210318 MGI PMID:33569080 1551580 Gcsh glycine cleavage system protein H (aminomethyl carrier) gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20210318 MGI PMID:33569080 1551580 Gcsh glycine cleavage system protein H (aminomethyl carrier) gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20210318 MGI PMID:33569080 1551580 Gcsh glycine cleavage system protein H (aminomethyl carrier) gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20210318 MGI PMID:33569080 1551580 Gcsh glycine cleavage system protein H (aminomethyl carrier) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:33569080 1551580 Gcsh glycine cleavage system protein H (aminomethyl carrier) gene MP:0003900 shortened QT interval IEA N RGD:5509061 20230601 MGI 1551580 Gcsh glycine cleavage system protein H (aminomethyl carrier) gene MP:0006386 absent somites IAGP N RGD:5509061 20210318 MGI PMID:33569080 1551580 Gcsh glycine cleavage system protein H (aminomethyl carrier) gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20230601 MGI 1551580 Gcsh glycine cleavage system protein H (aminomethyl carrier) gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20210318 MGI PMID:33569080 1551580 Gcsh glycine cleavage system protein H (aminomethyl carrier) gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20210318 MGI PMID:33569080 1551580 Gcsh glycine cleavage system protein H (aminomethyl carrier) gene MP:0012165 absent neural folds IAGP N RGD:5509061 20210318 MGI PMID:33569080 1551580 Gcsh glycine cleavage system protein H (aminomethyl carrier) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551581 Slc4a8 solute carrier family 4 (anion exchanger), member 8 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1551581 Slc4a8 solute carrier family 4 (anion exchanger), member 8 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230601 MGI 1551581 Slc4a8 solute carrier family 4 (anion exchanger), member 8 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1551581 Slc4a8 solute carrier family 4 (anion exchanger), member 8 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:20389022 1551581 Slc4a8 solute carrier family 4 (anion exchanger), member 8 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20389022 1551587 Sec24c SEC24 homolog C, COPII coat complex component gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:24876386 1551587 Sec24c SEC24 homolog C, COPII coat complex component gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24876386 1551587 Sec24c SEC24 homolog C, COPII coat complex component gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24876386 1551588 Tmem63c transmembrane protein 63c gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1551588 Tmem63c transmembrane protein 63c gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1551588 Tmem63c transmembrane protein 63c gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1551588 Tmem63c transmembrane protein 63c gene MP:0001891 hydrocephaly IEA N RGD:5509061 20210520 MGI 1551588 Tmem63c transmembrane protein 63c gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210520 MGI 1551588 Tmem63c transmembrane protein 63c gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1551589 Spg7 SPG7, paraplegin matrix AAA peptidase subunit gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:14722615 1551589 Spg7 SPG7, paraplegin matrix AAA peptidase subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14722615 1551589 Spg7 SPG7, paraplegin matrix AAA peptidase subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:14722615 1551589 Spg7 SPG7, paraplegin matrix AAA peptidase subunit gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:14722615 1551589 Spg7 SPG7, paraplegin matrix AAA peptidase subunit gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:14722615 1551589 Spg7 SPG7, paraplegin matrix AAA peptidase subunit gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:14722615 1551589 Spg7 SPG7, paraplegin matrix AAA peptidase subunit gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:14722615 1551589 Spg7 SPG7, paraplegin matrix AAA peptidase subunit gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:14722615 1551589 Spg7 SPG7, paraplegin matrix AAA peptidase subunit gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:14722615 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0000125 absent incisors IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0000373 belly spot IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0000380 small hair follicles IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0000745 tremors IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230601 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0001304 cataract IEA N RGD:5509061 20230601 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0001512 trunk curl IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20220811 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0001577 anemia IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220811 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20181227 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0002965 increased circulating serum albumin level IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0004380 short frontal bone IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0004757 abnormal distal convoluted tubule morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0004790 absent upper incisors IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0004791 absent lower incisors IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0005367 renal/urinary system phenotype IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0005507 tail dragging IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0005540 decreased urine albumin level IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0005542 cornea vascularization IEA N RGD:5509061 20230601 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20220811 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20231207 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20230601 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0008806 increased circulating amylase level IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0009051 dilated distal convoluted tubule IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0011424 decreased urine uric acid level IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0011435 increased urine magnesium level IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0011585 decreased alkaline phosphatase activity IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20210304 MGI PMID:28818080 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0012121 sclerocornea IEA N RGD:5509061 20230601 MGI 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0012725 small sebaceous gland IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0013370 anhidrosis IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0013458 decreased eccrine gland number IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0030178 abnormal scalp morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0030431 wide metopic suture IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551590 Kctd1 potassium channel tetramerisation domain containing 1 gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 1551591 Gpr173 G-protein coupled receptor 173 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1551591 Gpr173 G-protein coupled receptor 173 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20190502 MGI 1551591 Gpr173 G-protein coupled receptor 173 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1551592 Wnt5b wingless-type MMTV integration site family, member 5B gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20231207 MGI 1551592 Wnt5b wingless-type MMTV integration site family, member 5B gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19285468 1551592 Wnt5b wingless-type MMTV integration site family, member 5B gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19285468 1551592 Wnt5b wingless-type MMTV integration site family, member 5B gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:19285468 1551592 Wnt5b wingless-type MMTV integration site family, member 5B gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1551592 Wnt5b wingless-type MMTV integration site family, member 5B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19285468 1551594 Zfp654 zinc finger protein 654 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230601 MGI 1551594 Zfp654 zinc finger protein 654 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1551594 Zfp654 zinc finger protein 654 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551598 Dstyk dual serine/threonine and tyrosine protein kinase gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20180329 MGI PMID:25400726 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10026148 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0001394 circling IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0001522 impaired swimming IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10026148 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20160526 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0004328 decreased vestibular hair cell number IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0004697 abnormal thyroid follicular cell morphology IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0005191 head tilt IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0005307 head tossing IAGP N RGD:5509061 20160526 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0005546 choroidal neovascularization IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10026148 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20231207 MGI 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:10026148 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20160512 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10026148 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20160526 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0012671 retina spots IAGP N RGD:5509061 20160526 MGI PMID:27090238 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551601 Ap1g1 adaptor protein complex AP-1, gamma 1 subunit gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:27090238 1551602 Pard6a par-6 family cell polarity regulator alpha gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0000111 cleft palate IEA N RGD:5509061 20210520 MGI 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20200402 MGI 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:23636699 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:20439742 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:20439742 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:10555141 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:15215868 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:23636699 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20439742 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15215868 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10555141 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20220519 MGI 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16581773 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20220519 MGI 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20220519 MGI 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10555141 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0004375 enlarged frontal bone IAGP N RGD:5509061 20141003 MGI PMID:20439742 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0004379 wide frontal bone IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0004386 enlarged interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:20439742 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:20439742 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:20439742 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:20439742 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:10555141 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:17182866 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:20439742 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20439742 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10555141 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15215868 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10555141 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16501171 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23636699 1551604 Dnmt3b DNA methyltransferase 3B gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20141003 MGI PMID:23636699 1551608 Usp19 ubiquitin specific peptidase 19 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151203 MGI PMID:26048142 1551608 Usp19 ubiquitin specific peptidase 19 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201022 MGI 1551608 Usp19 ubiquitin specific peptidase 19 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20151203 MGI PMID:26048142 1551608 Usp19 ubiquitin specific peptidase 19 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1551608 Usp19 ubiquitin specific peptidase 19 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1551608 Usp19 ubiquitin specific peptidase 19 gene MP:0004064 decreased susceptibility to induced muscular atrophy IAGP N RGD:5509061 20151203 MGI PMID:26048142 1551608 Usp19 ubiquitin specific peptidase 19 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1551608 Usp19 ubiquitin specific peptidase 19 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20181227 MGI 1551608 Usp19 ubiquitin specific peptidase 19 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20151203 MGI PMID:26048142 1551608 Usp19 ubiquitin specific peptidase 19 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20151203 MGI PMID:26048142 1551608 Usp19 ubiquitin specific peptidase 19 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20151203 MGI PMID:26048142 1551608 Usp19 ubiquitin specific peptidase 19 gene MP:0010052 increased grip strength IAGP N RGD:5509061 20151203 MGI PMID:26048142 1551608 Usp19 ubiquitin specific peptidase 19 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551612 Nudcd2 NudC domain containing 2 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20230601 MGI 1551612 Nudcd2 NudC domain containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1551612 Nudcd2 NudC domain containing 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1551615 Cct5 chaperonin containing TCP1 subunit 5 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220519 MGI 1551615 Cct5 chaperonin containing TCP1 subunit 5 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1551615 Cct5 chaperonin containing TCP1 subunit 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1551615 Cct5 chaperonin containing TCP1 subunit 5 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200402 MGI 1551615 Cct5 chaperonin containing TCP1 subunit 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1551615 Cct5 chaperonin containing TCP1 subunit 5 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20221215 MGI 1551615 Cct5 chaperonin containing TCP1 subunit 5 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1551615 Cct5 chaperonin containing TCP1 subunit 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1551615 Cct5 chaperonin containing TCP1 subunit 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551616 Hdac5 histone deacetylase 5 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15367668 1551616 Hdac5 histone deacetylase 5 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15367668 1551616 Hdac5 histone deacetylase 5 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16678093 1551616 Hdac5 histone deacetylase 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15367668 1551616 Hdac5 histone deacetylase 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15367668 1551616 Hdac5 histone deacetylase 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15367668 1551616 Hdac5 histone deacetylase 5 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:20181743 1551616 Hdac5 histone deacetylase 5 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:17786239 1551616 Hdac5 histone deacetylase 5 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15367668 1551616 Hdac5 histone deacetylase 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15367668 1551616 Hdac5 histone deacetylase 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20181743 1551616 Hdac5 histone deacetylase 5 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15367668 1551619 Rph3al rabphilin 3A-like (without C2 domains) gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15159548 1551619 Rph3al rabphilin 3A-like (without C2 domains) gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15159548 1551619 Rph3al rabphilin 3A-like (without C2 domains) gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15159548 1551619 Rph3al rabphilin 3A-like (without C2 domains) gene MP:0009161 pancreatic acinar cell zymogen granule accumulation IAGP N RGD:5509061 20141003 MGI PMID:15159548 1551620 Aldh1l2 aldehyde dehydrogenase 1 family, member L2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20210204 MGI PMID:33168096 1551620 Aldh1l2 aldehyde dehydrogenase 1 family, member L2 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20210204 MGI PMID:33168096 1551620 Aldh1l2 aldehyde dehydrogenase 1 family, member L2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20210204 MGI PMID:33168096 1551620 Aldh1l2 aldehyde dehydrogenase 1 family, member L2 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20210204 MGI PMID:33168096 1551620 Aldh1l2 aldehyde dehydrogenase 1 family, member L2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20210204 MGI PMID:33168096 1551620 Aldh1l2 aldehyde dehydrogenase 1 family, member L2 gene MP:0011229 abnormal vitamin C level IAGP N RGD:5509061 20210204 MGI PMID:33168096 1551620 Aldh1l2 aldehyde dehydrogenase 1 family, member L2 gene MP:0011230 abnormal folic acid level IAGP N RGD:5509061 20210204 MGI PMID:33168096 1551620 Aldh1l2 aldehyde dehydrogenase 1 family, member L2 gene MP:0012604 decreased glutathione level IAGP N RGD:5509061 20210204 MGI PMID:33168096 1551620 Aldh1l2 aldehyde dehydrogenase 1 family, member L2 gene MP:0014174 decreased fatty acid beta-oxidation IAGP N RGD:5509061 20210204 MGI PMID:33168096 1551620 Aldh1l2 aldehyde dehydrogenase 1 family, member L2 gene MP:0030623 decreased cysteine level IAGP N RGD:5509061 20210204 MGI PMID:33168096 1551620 Aldh1l2 aldehyde dehydrogenase 1 family, member L2 gene MP:0030685 decreased cystathionine level IAGP N RGD:5509061 20210204 MGI PMID:33168096 1551622 Btla B and T lymphocyte associated gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:12796776 1551622 Btla B and T lymphocyte associated gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:15128774 1551622 Btla B and T lymphocyte associated gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:16237069 1551622 Btla B and T lymphocyte associated gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:19342624 1551622 Btla B and T lymphocyte associated gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:16237069 1551622 Btla B and T lymphocyte associated gene MP:0004752 decreased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:16237069 1551622 Btla B and T lymphocyte associated gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12796776 1551622 Btla B and T lymphocyte associated gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16237069 1551622 Btla B and T lymphocyte associated gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12796776 1551622 Btla B and T lymphocyte associated gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12796776 1551622 Btla B and T lymphocyte associated gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16237069 1551622 Btla B and T lymphocyte associated gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12796776 1551622 Btla B and T lymphocyte associated gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12796776 1551622 Btla B and T lymphocyte associated gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:12796776 1551622 Btla B and T lymphocyte associated gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16237069 1551622 Btla B and T lymphocyte associated gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:16237069 1551622 Btla B and T lymphocyte associated gene MP:0008749 abnormal peripheral T cell anergy IAGP N RGD:5509061 20141003 MGI PMID:19342624 1551626 Dad1 defender against cell death 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:10336695 1551626 Dad1 defender against cell death 1 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:10748466 1551626 Dad1 defender against cell death 1 gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10336695 1551626 Dad1 defender against cell death 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:10336695 1551626 Dad1 defender against cell death 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10748466 1551626 Dad1 defender against cell death 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10336695 1551626 Dad1 defender against cell death 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10748466 1551626 Dad1 defender against cell death 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10336695 1551626 Dad1 defender against cell death 1 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0011187 abnormal parietal endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0011197 abnormal proamniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0011200 abnormal extraembryonic coelom morphology IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0012095 increased Reichert's membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0012299 hydropic allantois IAGP N RGD:5509061 20141003 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:10720432 1551626 Dad1 defender against cell death 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:10748466 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10197978 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9620849 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15585856 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9620849 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:9620849 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21640975 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10197978 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12874264 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9620849 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10197978 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000709 enlarged thymus IEA N RGD:5509061 20111116 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:9620849 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001182 lung hemorrhage IEA N RGD:5509061 20141003 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9620849 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15831701 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17585010 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:21640975 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001861 lung inflammation IEA N RGD:5509061 20141003 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002023 increased B cell derived lymphoma incidence IEA N RGD:5509061 20141003 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10197978 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9620849 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002083 premature death IAGP N RGD:5509061 20191128 MGI PMID:22078222 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9620849 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002144 abnormal B cell differentiation IEA N RGD:5509061 20111116 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002145 abnormal T cell differentiation IEA N RGD:5509061 20190418 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15831701 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9620849 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:10606629 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10197978 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15585856 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17312133 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10606629 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002445 abnormal mononuclear cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15585856 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002463 abnormal neutrophil physiology IEA N RGD:5509061 20111116 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002465 abnormal eosinophil physiology IEA N RGD:5509061 20111116 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002493 increased IgG level IAGP N RGD:5509061 20191128 MGI PMID:22078222 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:17347685 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:21640975 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0002619 abnormal lymphocyte morphology IEA N RGD:5509061 20190418 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21640975 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20191128 MGI PMID:22078222 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:15944314 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10606629 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20191128 MGI PMID:22078222 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20191128 MGI PMID:22078222 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20191128 MGI PMID:22078222 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20191128 MGI PMID:22078222 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15831701 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20191128 MGI PMID:22078222 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0004944 abnormal B cell negative selection IAGP N RGD:5509061 20191128 MGI PMID:22078222 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:9620849 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20190418 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9620849 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10197978 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20191128 MGI PMID:22078222 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17585010 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005068 abnormal NK cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11896280 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005070 impaired natural killer cell mediated cytotoxicity IEA N RGD:5509061 20111116 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17585010 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005079 decreased cytotoxic T cell cytolysis IEA N RGD:5509061 20111116 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005150 cachexia IEA N RGD:5509061 20111116 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005333 decreased heart rate IEA N RGD:5509061 20190418 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10606629 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:17347685 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005673 decreased susceptibility to graft versus host disease IAGP N RGD:5509061 20141003 MGI PMID:11896280 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005673 decreased susceptibility to graft versus host disease IAGP N RGD:5509061 20141003 MGI PMID:15585856 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0005673 decreased susceptibility to graft versus host disease IAGP N RGD:5509061 20141003 MGI PMID:17312133 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:17347685 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:11896280 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20180215 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20190418 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20191128 MGI PMID:22078222 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:9620849 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008112 abnormal monocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:9620849 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:15585856 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:12874264 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15831701 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008240 abnormal spleen marginal zone macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:12874264 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17312133 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:17585010 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008560 increased tumor necrosis factor secretion IEA N RGD:5509061 20190418 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008564 increased interferon-beta secretion IEA N RGD:5509061 20190418 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:17585010 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:15831701 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21421839 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008744 abnormal B cell anergy IAGP N RGD:5509061 20191128 MGI PMID:22078222 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:17585010 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:21640975 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:9736736 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0008802 abnormal intestinal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21640975 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10606629 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0009317 increased follicular lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0009318 increased splenic marginal zone lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20141003 MGI PMID:21640975 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:17347685 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10606629 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:9620849 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:12161749 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20956547 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 1551628 Inpp5d inositol polyphosphate-5-phosphatase D gene MP:0014471 enhanced B cell migration IAGP N RGD:5509061 20240613 MGI PMID:10606629 1551629 4930453N24Rik RIKEN cDNA 4930453N24 gene gene MP:0000018 small ears IAGP N RGD:5509061 20150730 MGI PMID:8830097 1551629 4930453N24Rik RIKEN cDNA 4930453N24 gene gene MP:0000120 malocclusion IAGP N RGD:5509061 20180215 MGI PMID:8830097 1551629 4930453N24Rik RIKEN cDNA 4930453N24 gene gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20180215 MGI PMID:8830097 1551629 4930453N24Rik RIKEN cDNA 4930453N24 gene gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20150730 MGI PMID:8830097 1551629 4930453N24Rik RIKEN cDNA 4930453N24 gene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20150730 MGI PMID:8830097 1551629 4930453N24Rik RIKEN cDNA 4930453N24 gene gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20150730 MGI PMID:8830097 1551629 4930453N24Rik RIKEN cDNA 4930453N24 gene gene MP:0002083 premature death IAGP N RGD:5509061 20150730 MGI PMID:8830097 1551629 4930453N24Rik RIKEN cDNA 4930453N24 gene gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20150730 MGI PMID:8830097 1551629 4930453N24Rik RIKEN cDNA 4930453N24 gene gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20150730 MGI PMID:8830097 1551629 4930453N24Rik RIKEN cDNA 4930453N24 gene gene MP:0030542 abnormal dentin development IAGP N RGD:5509061 20180215 MGI PMID:8830097 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20200310 MGI PMID:24401273 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20200310 MGI PMID:24401273 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:22634729 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:18585372 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:18585372 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:22634729 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20200310 MGI PMID:18585372 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0002284 abnormal tracheal smooth muscle morphology IAGP N RGD:5509061 20200310 MGI PMID:18585372 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:18585372 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20200310 MGI PMID:24476694 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0002871 albuminuria IAGP N RGD:5509061 20200310 MGI PMID:24476694 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20200310 MGI PMID:24476694 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20200310 MGI PMID:24401273 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:18585372 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:24401273 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20200310 MGI PMID:24476694 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20200310 MGI PMID:24401273 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20200310 MGI PMID:24401273 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20200310 MGI PMID:24401273 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20200310 MGI PMID:24476694 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20200310 MGI PMID:24476694 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200310 MGI PMID:18585372 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:24476694 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0010988 abnormal bronchial cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:18585372 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0010994 aerophagia IAGP N RGD:5509061 20200310 MGI PMID:18585372 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18585372 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24401273 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0011460 decreased urine chloride ion level IAGP N RGD:5509061 20200310 MGI PMID:24476694 1551631 Ano1 anoctamin 1, calcium activated chloride channel gene MP:0014208 decreased intestinal epithelial chloride transmembrane transport IAGP N RGD:5509061 20200310 MGI PMID:24974903 1551632 Fkbp4 FK506 binding protein 4 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:16176985 1551632 Fkbp4 FK506 binding protein 4 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:17307907 1551632 Fkbp4 FK506 binding protein 4 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:16873445 1551632 Fkbp4 FK506 binding protein 4 gene MP:0000664 small prostate gland anterior lobe IAGP N RGD:5509061 20141003 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20231207 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20231207 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0000692 small spleen IEA N RGD:5509061 20231207 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20231207 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001147 small testis IEA N RGD:5509061 20231207 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230601 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20191226 MGI PMID:16176985 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16176985 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17307907 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16176985 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16873445 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0002059 abnormal seminal vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20231207 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17307907 1551632 Fkbp4 FK506 binding protein 4 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0002771 absent prostate gland anterior lobe IAGP N RGD:5509061 20141003 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0003124 hypospadia IAGP N RGD:5509061 20141003 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0003124 hypospadia IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20210128 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0003553 abnormal foreskin morphology IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:16873445 1551632 Fkbp4 FK506 binding protein 4 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0004930 small epididymis IEA N RGD:5509061 20231207 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20231207 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0005187 abnormal penis morphology IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0005188 small penis IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20231207 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0006415 absent testes IEA N RGD:5509061 20231207 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0009198 abnormal male genitalia morphology IEA N RGD:5509061 20231207 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:17307907 1551632 Fkbp4 FK506 binding protein 4 gene MP:0009662 abnormal uterine receptivity IAGP N RGD:5509061 20191226 MGI PMID:16176985 1551632 Fkbp4 FK506 binding protein 4 gene MP:0009664 abnormal luminal closure IAGP N RGD:5509061 20191226 MGI PMID:16176985 1551632 Fkbp4 FK506 binding protein 4 gene MP:0009735 abnormal prostate gland development IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20231207 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551632 Fkbp4 FK506 binding protein 4 gene MP:0031286 unilateral cryptorchism IAGP N RGD:5509061 20211014 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0031294 penile hypospadia IAGP N RGD:5509061 20211014 MGI PMID:17142810 1551632 Fkbp4 FK506 binding protein 4 gene MP:0031378 ambiguous external male genitalia IAGP N RGD:5509061 20220421 MGI PMID:15831525 1551632 Fkbp4 FK506 binding protein 4 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:16873445 1551634 Apom apolipoprotein M gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18381283 1551634 Apom apolipoprotein M gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1551634 Apom apolipoprotein M gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18006500 1551634 Apom apolipoprotein M gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1551634 Apom apolipoprotein M gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210520 MGI 1551634 Apom apolipoprotein M gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:18006500 1551634 Apom apolipoprotein M gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20201022 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20181227 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0000322 increased granulocyte number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20181227 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0001916 intracerebral hemorrhage IEA N RGD:5509061 20170504 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20181227 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170504 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20181227 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20181227 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0003036 vertebral transformation IEA N RGD:5509061 20181227 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20181227 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0004794 increased anti-nuclear antigen antibody level IEA N RGD:5509061 20201022 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20170105 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20170504 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20170105 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20181227 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0008097 increased plasma cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0008173 increased follicular B cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0008182 decreased marginal zone B cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0008206 increased B-2 B cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0008346 increased gamma-delta T cell number IEA N RGD:5509061 20181227 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20181227 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0009820 abnormal liver vasculature morphology IEA N RGD:5509061 20170504 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0009926 decreased transitional stage T2 B cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0010490 abnormal inferior vena cava valve morphology IEA N RGD:5509061 20170504 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IEA N RGD:5509061 20201022 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0010851 decreased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20170504 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20181227 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0012767 increased KLRG1-positive NK cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013022 increased Ly6C high monocyte number IEA N RGD:5509061 20170105 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013154 increased KLRG1+ CD8 alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013157 increased KLRG1+ CD4 alpha-beta T cell number IEA N RGD:5509061 20181227 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013417 decreased memory-marker gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013418 increased memory-marker gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013421 increased CD5-positive gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013426 decreased memory-marker NK cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013427 increased memory-marker NK cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013430 increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013433 increased KLRG1-positive CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013511 increased CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013513 decreased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013519 decreased CD4-positive NK T cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013522 decreased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013669 decreased Ly6C-positive immature NK cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013675 decreased Ly6C-positive mature NK cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013764 decreased T-helper cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013775 increased KLRG1-positive T-helper cell number IEA N RGD:5509061 20201231 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20170504 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0013975 abnormal coronary sinus connection IEA N RGD:5509061 20170504 MGI 1551639 Cog6 component of oligomeric golgi complex 6 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1551641 Tsnax translin-associated factor X gene MP:0001258 decreased body length IEA N RGD:5509061 20240523 MGI 1551641 Tsnax translin-associated factor X gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20240523 MGI 1551641 Tsnax translin-associated factor X gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20240523 MGI 1551641 Tsnax translin-associated factor X gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 1551641 Tsnax translin-associated factor X gene MP:0002834 decreased heart weight IEA N RGD:5509061 20240523 MGI 1551641 Tsnax translin-associated factor X gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20211230 MGI PMID:26096928 1551641 Tsnax translin-associated factor X gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20211230 MGI PMID:26096928 1551641 Tsnax translin-associated factor X gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20211230 MGI PMID:26096928 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11416156 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20231207 MGI 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20231207 MGI 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20231207 MGI 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11416156 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20191219 MGI PMID:27707879 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20231207 MGI 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11416156 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20201022 MGI PMID:27430022 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20231207 MGI 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20231207 MGI 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11416156 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20231207 MGI 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20201022 MGI PMID:27430022 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20201022 MGI PMID:27430022 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:11416156 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20201022 MGI PMID:27430022 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11416156 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20201022 MGI PMID:27430022 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:11416156 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:11416156 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:11416156 1551642 Kirrel1 kirre like nephrin family adhesion molecule 1 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:11416156 1551651 Morc2a microrchidia 2A gene MP:0000026 abnormal inner ear morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000049 abnormal middle ear morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000075 absent neurocranium IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000104 abnormal sphenoid bone morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000141 abnormal vertebral body morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000149 abnormal scapula morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1551651 Morc2a microrchidia 2A gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000297 abnormal atrioventricular cushion morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000440 domed cranium IAGP N RGD:5509061 20230126 MGI PMID:36332029 1551651 Morc2a microrchidia 2A gene MP:0000454 abnormal jaw morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000550 abnormal forelimb morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000552 abnormal radius morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000553 absent radius IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000554 abnormal carpal bone morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000565 oligodactyly IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000613 abnormal salivary gland morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000614 absent salivary gland IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000632 abnormal pineal gland morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000633 abnormal pituitary gland morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000705 athymia IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000706 small thymus IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000819 abnormal olfactory bulb morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000820 abnormal choroid plexus morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0000899 abnormal corpora quadrigemina morphology IAGP N RGD:5509061 20230126 MGI PMID:36332029 1551651 Morc2a microrchidia 2A gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0001014 absent superior cervical ganglion IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0001067 absent mandibular nerve IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0001093 small trigeminal ganglion IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0001127 small ovary IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230126 MGI PMID:36332029 1551651 Morc2a microrchidia 2A gene MP:0001265 decreased body size IAGP N RGD:5509061 20230126 MGI PMID:36332029 1551651 Morc2a microrchidia 2A gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0001393 ataxia IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20230126 MGI PMID:36332029 1551651 Morc2a microrchidia 2A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20230126 MGI PMID:36332029 1551651 Morc2a microrchidia 2A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0001406 abnormal gait IEA N RGD:5509061 20210128 MGI 1551651 Morc2a microrchidia 2A gene MP:0001513 limb grasping IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20230126 MGI PMID:36332029 1551651 Morc2a microrchidia 2A gene MP:0001916 intracerebral hemorrhage IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0002083 premature death IAGP N RGD:5509061 20230126 MGI PMID:36332029 1551651 Morc2a microrchidia 2A gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0002237 abnormal nasal cavity morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0002239 abnormal nasal septum morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0002243 abnormal vomeronasal organ morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0002279 abnormal diaphragm morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0002768 small adrenal glands IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0002951 small thyroid gland IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0002989 small kidney IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0003078 aphakia IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0003327 liver cyst IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0003924 diaphragmatic hernia IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0004158 right aortic arch IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0004234 abnormal masticatory muscle morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0004247 small pancreas IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0004352 absent humerus IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0004440 absent occipital bone IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0004463 basisphenoid bone foramen IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0004666 absent stapedial artery IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0004668 absent vertebral body IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0004790 absent upper incisors IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20230126 MGI PMID:36332029 1551651 Morc2a microrchidia 2A gene MP:0005105 abnormal middle ear ossicle morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0005107 abnormal stapes morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0005108 abnormal ulna morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0005113 decreased spinal cord ventral horn cell number IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0005157 holoprosencephaly IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0005236 abnormal olfactory nerve morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0005238 increased brain size IAGP N RGD:5509061 20230126 MGI PMID:36332029 1551651 Morc2a microrchidia 2A gene MP:0005269 abnormal occipital bone morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0005298 abnormal clavicle morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0005315 absent pituitary gland IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0005358 abnormal incisor morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0005587 abnormal Meckel's cartilage morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0006033 abnormal external auditory canal morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0006425 absent Mullerian ducts IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0008128 abnormal brain internal capsule morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0008797 facial cleft IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0008923 thoracoschisis IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0009073 absent Wolffian ducts IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0009434 paraparesis IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20230126 MGI PMID:36332029 1551651 Morc2a microrchidia 2A gene MP:0009495 abnormal common bile duct morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0009569 abnormal left lung morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0009570 abnormal right lung morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0009707 absent external auditory canal IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0009771 absent optic chiasm IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0009820 abnormal liver vasculature morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0009904 tongue hypoplasia IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0009917 abnormal hyoid bone body morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20230126 MGI PMID:36332029 1551651 Morc2a microrchidia 2A gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0010434 double inlet heart right ventricle IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0010465 aberrant origin of the right subclavian artery IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0010496 abnormal pectinate muscle morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20230126 MGI PMID:36332029 1551651 Morc2a microrchidia 2A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551651 Morc2a microrchidia 2A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0011380 enlarged brain ventricles IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0012091 increased midbrain size IAGP N RGD:5509061 20230126 MGI PMID:36332029 1551651 Morc2a microrchidia 2A gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1551651 Morc2a microrchidia 2A gene MP:0013816 absent digastric muscle IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013822 abnormal anterior cerebral artery morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013823 absent segment of anterior cerebral artery IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013830 abnormal intrathoracic topology of vagus nerve IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013851 abnormal Wolffian duct topology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013854 abnormal celiac artery morphology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013865 abnormal dorsal pancreas topology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013874 abnormal ductus venosus topology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013875 increased trigeminal neuroma incidence IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013914 absent intracranial segment of vertebral artery IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013927 abnormal facial nerve topology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013929 absent eye muscles IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013931 abnormal olfactory bulb position IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013932 fragmented Meckel's cartilage IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013936 abnormal thymus topology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013943 abnormal ureter topology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013952 retroesophageal left subclavian artery IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013953 left sided brachiocephalic trunk IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013970 absent connection between subcutaneous lymph vessels and lymph sac IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013979 abnormal subclavian artery origin IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013987 absent intrahepatic inferior vena cava segment IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013992 persistent dorsal ophthalmic artery IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013996 abnormal vertebral artery origin IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0013997 abnormal internal carotid artery topology IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0014006 absent posterior communicating artery IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0014021 heterochrony IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0014023 abnormal intestine placement IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0014110 absent ventral pancreas IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0014111 small ventral pancreas IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0014113 small dorsal pancreas IEA N RGD:5509061 20200310 MGI 1551651 Morc2a microrchidia 2A gene MP:0014114 abnormal cognition IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20240215 MGI PMID:34695197 1551651 Morc2a microrchidia 2A gene MP:0020301 short tongue IEA N RGD:5509061 20200310 MGI 1551652 Nfya nuclear transcription factor-Y alpha gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:14678971 1551652 Nfya nuclear transcription factor-Y alpha gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14678971 1551652 Nfya nuclear transcription factor-Y alpha gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20150212 MGI PMID:14678971 1551652 Nfya nuclear transcription factor-Y alpha gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:14678971 1551654 Pou6f2 POU domain, class 6, transcription factor 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20200310 MGI 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:21909103 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:11051546 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:21909103 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:22068587 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000119 abnormal tooth eruption IAGP N RGD:5509061 20160825 MGI PMID:24127173 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:10984520 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:11051546 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:21909103 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:22068587 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22068587 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:21909103 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:21909103 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10984520 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20161013 MGI PMID:26659571 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11085748 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22068587 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22068587 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22068587 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22068587 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160825 MGI PMID:24127173 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0002351 abnormal cervical lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:11085748 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:11085748 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:10984520 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10984520 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:10984520 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:10984520 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20161013 MGI PMID:26659571 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:21909103 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10984520 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:10984520 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:10984520 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004983 abnormal osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:21909103 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:10984520 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:11085748 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:21909103 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:22068587 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:22068587 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0005352 small cranium IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:22068587 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:11051546 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:10984520 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:21909103 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22068587 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20160825 MGI PMID:24127173 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008119 decreased Langerhans cell number IAGP N RGD:5509061 20141003 MGI PMID:18606662 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008162 increased diameter of tibia IAGP N RGD:5509061 20141003 MGI PMID:10984520 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008233 abnormal pro-B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008464 absent peripheral lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11085748 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008464 absent peripheral lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008465 absent mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11085748 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008465 absent mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11085748 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:10984520 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21441458 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0009633 absent cervical lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11085748 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0009917 abnormal hyoid bone body morphology IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:11051546 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:22068587 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:22068587 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:21909103 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:21909105 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0011999 abnormal tail length IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0013614 abnormal areal bone mineral density IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0013617 increased areal bone mineral density IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0013619 abnormal long bone internal diameter IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0013619 abnormal long bone internal diameter IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0013621 decreased internal diameter of femur IAGP N RGD:5509061 20151112 MGI PMID:26234751 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20220922 MGI PMID:21909103 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:10984520 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:21909103 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20160818 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20220922 MGI PMID:21909103 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0030072 round face IAGP N RGD:5509061 20170921 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0030279 thin neurocranium IAGP N RGD:5509061 20171102 MGI PMID:9950424 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0030469 optic canal stenosis IAGP N RGD:5509061 20171221 MGI PMID:22836362 1551655 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11 gene MP:0031278 decreased osteosarcoma incidence IAGP N RGD:5509061 20210805 MGI PMID:26659571 1551656 M6pr mannose-6-phosphate receptor, cation dependent gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1551656 M6pr mannose-6-phosphate receptor, cation dependent gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8806828 1551656 M6pr mannose-6-phosphate receptor, cation dependent gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 1551656 M6pr mannose-6-phosphate receptor, cation dependent gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1551656 M6pr mannose-6-phosphate receptor, cation dependent gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:8806828 1551656 M6pr mannose-6-phosphate receptor, cation dependent gene MP:0003174 increased lysosomal enzyme secretion IAGP N RGD:5509061 20141003 MGI PMID:8262065 1551656 M6pr mannose-6-phosphate receptor, cation dependent gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1551656 M6pr mannose-6-phosphate receptor, cation dependent gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20141003 MGI PMID:8262065 1551656 M6pr mannose-6-phosphate receptor, cation dependent gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:11105922 1551656 M6pr mannose-6-phosphate receptor, cation dependent gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:8262065 1551656 M6pr mannose-6-phosphate receptor, cation dependent gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 1551656 M6pr mannose-6-phosphate receptor, cation dependent gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8262065 1551656 M6pr mannose-6-phosphate receptor, cation dependent gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8806828 1551656 M6pr mannose-6-phosphate receptor, cation dependent gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8262064 1551656 M6pr mannose-6-phosphate receptor, cation dependent gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1551657 Robo4 roundabout guidance receptor 4 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:24355925 1551657 Robo4 roundabout guidance receptor 4 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18345009 1551657 Robo4 roundabout guidance receptor 4 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:22123939 1551657 Robo4 roundabout guidance receptor 4 gene MP:0001619 abnormal vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:18345009 1551657 Robo4 roundabout guidance receptor 4 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:24355925 1551657 Robo4 roundabout guidance receptor 4 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:18345009 1551657 Robo4 roundabout guidance receptor 4 gene MP:0003711 pathological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:18345009 1551657 Robo4 roundabout guidance receptor 4 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:24355925 1551657 Robo4 roundabout guidance receptor 4 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20201015 MGI PMID:30825241 1551657 Robo4 roundabout guidance receptor 4 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20201015 MGI PMID:30825241 1551657 Robo4 roundabout guidance receptor 4 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20201015 MGI PMID:30825241 1551657 Robo4 roundabout guidance receptor 4 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20201015 MGI PMID:30825241 1551657 Robo4 roundabout guidance receptor 4 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:24355925 1551657 Robo4 roundabout guidance receptor 4 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20201015 MGI PMID:30825241 1551657 Robo4 roundabout guidance receptor 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1551657 Robo4 roundabout guidance receptor 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210422 MGI 1551657 Robo4 roundabout guidance receptor 4 gene MP:0011132 abnormal lung endothelial cell migration IAGP N RGD:5509061 20211125 MGI PMID:18345009 1551657 Robo4 roundabout guidance receptor 4 gene MP:0012107 enhanced exercise endurance IAGP N RGD:5509061 20201015 MGI PMID:30825241 1551657 Robo4 roundabout guidance receptor 4 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20201015 MGI PMID:30825241 1551659 Esam endothelial cell-specific adhesion molecule gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12819200 1551659 Esam endothelial cell-specific adhesion molecule gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16818677 1551659 Esam endothelial cell-specific adhesion molecule gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12819200 1551659 Esam endothelial cell-specific adhesion molecule gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:16818677 1551659 Esam endothelial cell-specific adhesion molecule gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:16818677 1551659 Esam endothelial cell-specific adhesion molecule gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12819200 1551659 Esam endothelial cell-specific adhesion molecule gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:16818677 1551664 Iqcg IQ motif containing G gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:12855593 1551664 Iqcg IQ motif containing G gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:12855593 1551664 Iqcg IQ motif containing G gene MP:0001925 male infertility IAGP N RGD:5509061 20220324 MGI PMID:24849454 1551664 Iqcg IQ motif containing G gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20200310 MGI PMID:24362311 1551664 Iqcg IQ motif containing G gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220324 MGI PMID:24849454 1551664 Iqcg IQ motif containing G gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20220324 MGI PMID:24849454 1551664 Iqcg IQ motif containing G gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220324 MGI PMID:24849454 1551664 Iqcg IQ motif containing G gene MP:0002675 asthenozoospermia IEA N RGD:5509061 20200310 MGI 1551664 Iqcg IQ motif containing G gene MP:0002687 oligozoospermia IEA N RGD:5509061 20200310 MGI 1551664 Iqcg IQ motif containing G gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:12855593 1551664 Iqcg IQ motif containing G gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:24362311 1551664 Iqcg IQ motif containing G gene MP:0005578 teratozoospermia IEA N RGD:5509061 20200310 MGI 1551664 Iqcg IQ motif containing G gene MP:0008545 absent sperm flagellum IEA N RGD:5509061 20200310 MGI 1551664 Iqcg IQ motif containing G gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220324 MGI PMID:24849454 1551664 Iqcg IQ motif containing G gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220324 MGI PMID:24849454 1551664 Iqcg IQ motif containing G gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220324 MGI PMID:24849454 1551664 Iqcg IQ motif containing G gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220324 MGI PMID:24849454 1551664 Iqcg IQ motif containing G gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220324 MGI PMID:24849454 1551664 Iqcg IQ motif containing G gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220324 MGI PMID:24849454 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20170105 MGI 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0001265 decreased body size IEA N RGD:5509061 20230824 MGI 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0001759 increased urine glucose level IEA N RGD:5509061 20211021 MGI 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0002959 increased urine microalbumin level IEA N RGD:5509061 20211021 MGI 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20211021 MGI 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20220630 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20201022 MGI 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0011085 postnatal lethality, complete penetrance IEA N RGD:5509061 20230824 MGI 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0011128 increased tertiary ovarian follicle number IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0030973 impaired gluconeogenesis IAGP N RGD:5509061 20200116 MGI PMID:28973305 1551668 Agpat1 1-acylglycerol-3-phosphate O-acyltransferase 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:28973305 1551670 Arhgap26 Rho GTPase activating protein 26 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20201022 MGI 1551670 Arhgap26 Rho GTPase activating protein 26 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20221215 MGI 1551670 Arhgap26 Rho GTPase activating protein 26 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1551670 Arhgap26 Rho GTPase activating protein 26 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20150910 MGI PMID:25019370 1551670 Arhgap26 Rho GTPase activating protein 26 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20211125 MGI PMID:25019370 1551670 Arhgap26 Rho GTPase activating protein 26 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:25019370 1551670 Arhgap26 Rho GTPase activating protein 26 gene MP:0030959 abnormal myoblast fusion IAGP N RGD:5509061 20211125 MGI PMID:25019370 1551679 Pla2g2f phospholipase A2, group IIF gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1551679 Pla2g2f phospholipase A2, group IIF gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1551679 Pla2g2f phospholipase A2, group IIF gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1551679 Pla2g2f phospholipase A2, group IIF gene MP:0001147 small testis IEA N RGD:5509061 20230119 MGI 1551679 Pla2g2f phospholipase A2, group IIF gene MP:0001262 decreased body weight IEA N RGD:5509061 20230119 MGI 1551679 Pla2g2f phospholipase A2, group IIF gene MP:0001297 microphthalmia IEA N RGD:5509061 20230119 MGI 1551679 Pla2g2f phospholipase A2, group IIF gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1551679 Pla2g2f phospholipase A2, group IIF gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 1551679 Pla2g2f phospholipase A2, group IIF gene MP:0010052 increased grip strength IEA N RGD:5509061 20230119 MGI 1551682 Ephb1 Eph receptor B1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1551682 Ephb1 Eph receptor B1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20201022 MGI 1551682 Ephb1 Eph receptor B1 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20201022 MGI 1551682 Ephb1 Eph receptor B1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1551682 Ephb1 Eph receptor B1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1551682 Ephb1 Eph receptor B1 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1551682 Ephb1 Eph receptor B1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:23143520 1551682 Ephb1 Eph receptor B1 gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20160526 MGI PMID:24997765 1551682 Ephb1 Eph receptor B1 gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:12971893 1551682 Ephb1 Eph receptor B1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20231207 MGI 1551682 Ephb1 Eph receptor B1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:12971893 1551682 Ephb1 Eph receptor B1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1551682 Ephb1 Eph receptor B1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20160526 MGI PMID:24997765 1551682 Ephb1 Eph receptor B1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20201022 MGI 1551682 Ephb1 Eph receptor B1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:23143520 1551682 Ephb1 Eph receptor B1 gene MP:0004267 abnormal optic tract morphology IAGP N RGD:5509061 20141003 MGI PMID:12971893 1551682 Ephb1 Eph receptor B1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19182796 1551682 Ephb1 Eph receptor B1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:21847105 1551682 Ephb1 Eph receptor B1 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20160526 MGI PMID:24997765 1551682 Ephb1 Eph receptor B1 gene MP:0008228 increased anterior commissure size IAGP N RGD:5509061 20160526 MGI PMID:24997765 1551682 Ephb1 Eph receptor B1 gene MP:0008960 abnormal axon pruning IAGP N RGD:5509061 20141003 MGI PMID:19182796 1551682 Ephb1 Eph receptor B1 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20160526 MGI PMID:24997765 1551682 Ephb1 Eph receptor B1 gene MP:0012462 decreased brain internal capsule size IAGP N RGD:5509061 20160526 MGI PMID:24997765 1551682 Ephb1 Eph receptor B1 gene MP:0012484 decreased corticospinal tract size IAGP N RGD:5509061 20160526 MGI PMID:24997765 1551682 Ephb1 Eph receptor B1 gene MP:0020140 increased brain external capsule size IAGP N RGD:5509061 20160616 MGI PMID:24997765 1551683 Herc4 hect domain and RLD 4 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17967448 1551683 Herc4 hect domain and RLD 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17967448 1551683 Herc4 hect domain and RLD 4 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1551683 Herc4 hect domain and RLD 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17967448 1551683 Herc4 hect domain and RLD 4 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1551683 Herc4 hect domain and RLD 4 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:17967448 1551685 Nme3 NME/NM23 nucleoside diphosphate kinase 3 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:22438820 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18056838 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20141003 MGI PMID:18056838 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:18056838 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:18056838 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18056838 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:18056838 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18056838 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:18176562 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18056838 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18056838 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22464323 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:18056838 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:18176562 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:18176562 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:18056838 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:18176562 1551687 Egln2 egl-9 family hypoxia-inducible factor 2 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18056838 1551688 Usp45 ubiquitin specific petidase 45 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20230601 MGI 1551688 Usp45 ubiquitin specific petidase 45 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20220901 MGI PMID:30573563 1551688 Usp45 ubiquitin specific petidase 45 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20220901 MGI PMID:30573563 1551688 Usp45 ubiquitin specific petidase 45 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220519 MGI 1551688 Usp45 ubiquitin specific petidase 45 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20220901 MGI PMID:30573563 1551689 Nenf neuron derived neurotrophic factor gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:24058337 1551689 Nenf neuron derived neurotrophic factor gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:24058337 1551689 Nenf neuron derived neurotrophic factor gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:24058337 1551689 Nenf neuron derived neurotrophic factor gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:24058337 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20200310 MGI 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0001258 decreased body length IAGP N RGD:5509061 20220106 MGI PMID:29809150 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20200310 MGI 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20220106 MGI PMID:29809150 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0004575 small limb buds IAGP N RGD:5509061 20220106 MGI PMID:29809150 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20200310 MGI 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20200310 MGI 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20220106 MGI PMID:29809150 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20220106 MGI PMID:29809150 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20220106 MGI PMID:29809150 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0011264 abnormal cardiac mesenchyme morphology IAGP N RGD:5509061 20220106 MGI PMID:29809150 1551690 Fbxl19 F-box and leucine-rich repeat protein 19 gene MP:0012177 delayed head development IAGP N RGD:5509061 20220106 MGI PMID:29809150 1551691 Corin corin, serine peptidase gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:15637153 1551691 Corin corin, serine peptidase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:18057101 1551691 Corin corin, serine peptidase gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20141003 MGI PMID:18057101 1551691 Corin corin, serine peptidase gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20141003 MGI PMID:20412777 1551691 Corin corin, serine peptidase gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20141003 MGI PMID:18057101 1551691 Corin corin, serine peptidase gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20141003 MGI PMID:20412777 1551691 Corin corin, serine peptidase gene MP:0000405 abnormal auchene hair morphology IAGP N RGD:5509061 20141003 MGI PMID:20412777 1551691 Corin corin, serine peptidase gene MP:0000423 delayed hair regrowth IAGP N RGD:5509061 20141003 MGI PMID:20412777 1551691 Corin corin, serine peptidase gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15637153 1551691 Corin corin, serine peptidase gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15637153 1551691 Corin corin, serine peptidase gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:15637153 1551691 Corin corin, serine peptidase gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:20412777 1551691 Corin corin, serine peptidase gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20141003 MGI PMID:15637153 1551691 Corin corin, serine peptidase gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15637153 1551691 Corin corin, serine peptidase gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15637153 1551691 Corin corin, serine peptidase gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20141003 MGI PMID:20412777 1551691 Corin corin, serine peptidase gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20141003 MGI PMID:20412777 1551691 Corin corin, serine peptidase gene MP:0008860 abnormal hair cycle telogen phase IAGP N RGD:5509061 20141003 MGI PMID:20412777 1551691 Corin corin, serine peptidase gene MP:0009272 decreased guard hair length IAGP N RGD:5509061 20141003 MGI PMID:20412777 1551691 Corin corin, serine peptidase gene MP:0011194 abnormal hair follicle physiology IAGP N RGD:5509061 20141003 MGI PMID:20412777 1551691 Corin corin, serine peptidase gene MP:0011195 increased hair follicle apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20412777 1551694 Dnajc16 DnaJ heat shock protein family (Hsp40) member C16 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1551694 Dnajc16 DnaJ heat shock protein family (Hsp40) member C16 gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20160811 MGI 1551694 Dnajc16 DnaJ heat shock protein family (Hsp40) member C16 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551696 Il18bp interleukin 18 binding protein gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0001263 weight loss IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0005014 increased B cell number IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0005152 pancytopenia IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20180531 MGI PMID:28900426 1551696 Il18bp interleukin 18 binding protein gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20180531 MGI PMID:28900426 1551696 Il18bp interleukin 18 binding protein gene MP:0008251 abnormal phagocyte morphology IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20180531 MGI PMID:28900426 1551696 Il18bp interleukin 18 binding protein gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20180531 MGI PMID:28900426 1551696 Il18bp interleukin 18 binding protein gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20180927 MGI PMID:29295842 1551696 Il18bp interleukin 18 binding protein gene MP:0012768 decreased KLRG1-positive NK cell number IAGP N RGD:5509061 20180531 MGI PMID:28900426 1551696 Il18bp interleukin 18 binding protein gene MP:0013667 increased immature NK cell number IAGP N RGD:5509061 20180531 MGI PMID:28900426 1551696 Il18bp interleukin 18 binding protein gene MP:0013672 decreased mature NK cell number IAGP N RGD:5509061 20180531 MGI PMID:28900426 1551699 Bcl2l2 BCL2-like 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:18551174 1551699 Bcl2l2 BCL2-like 2 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:18551174 1551699 Bcl2l2 BCL2-like 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18551174 1551699 Bcl2l2 BCL2-like 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9500547 1551699 Bcl2l2 BCL2-like 2 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:11420255 1551699 Bcl2l2 BCL2-like 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:11420255 1551699 Bcl2l2 BCL2-like 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20150402 MGI PMID:9770502 1551699 Bcl2l2 BCL2-like 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18551174 1551699 Bcl2l2 BCL2-like 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18551174 1551699 Bcl2l2 BCL2-like 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18551174 1551699 Bcl2l2 BCL2-like 2 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:9500547 1551699 Bcl2l2 BCL2-like 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9500547 1551699 Bcl2l2 BCL2-like 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20150402 MGI PMID:9770502 1551699 Bcl2l2 BCL2-like 2 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:9770502 1551699 Bcl2l2 BCL2-like 2 gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:11420255 1551699 Bcl2l2 BCL2-like 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:9500547 1551699 Bcl2l2 BCL2-like 2 gene MP:0002785 absent Leydig cells IAGP N RGD:5509061 20141003 MGI PMID:11420255 1551699 Bcl2l2 BCL2-like 2 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:18551174 1551699 Bcl2l2 BCL2-like 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11420255 1551699 Bcl2l2 BCL2-like 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:9500547 1551699 Bcl2l2 BCL2-like 2 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:11420255 1551699 Bcl2l2 BCL2-like 2 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:9500547 1551699 Bcl2l2 BCL2-like 2 gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:18551174 1551699 Bcl2l2 BCL2-like 2 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:18551174 1551699 Bcl2l2 BCL2-like 2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:18551174 1551699 Bcl2l2 BCL2-like 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20150402 MGI PMID:9770502 1551699 Bcl2l2 BCL2-like 2 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20141003 MGI PMID:11420255 1551699 Bcl2l2 BCL2-like 2 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20150402 MGI PMID:9770502 1551699 Bcl2l2 BCL2-like 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18551174 1551699 Bcl2l2 BCL2-like 2 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20150402 MGI PMID:9770502 1551699 Bcl2l2 BCL2-like 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:9770502 1551699 Bcl2l2 BCL2-like 2 gene MP:0014331 abnormal Purkinje cell mitochondrial morphology IAGP N RGD:5509061 20240718 MGI PMID:18551174 1551699 Bcl2l2 BCL2-like 2 gene MP:0020355 abnormal Sertoli cell barrier morphology IAGP N RGD:5509061 20160915 MGI PMID:11420255 1551699 Bcl2l2 BCL2-like 2 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220623 MGI PMID:9770502 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20201022 MGI 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20220519 MGI 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210520 MGI 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0002764 short tibia IEA N RGD:5509061 20201022 MGI 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201022 MGI 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210520 MGI 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1551706 Phf20l1 PHD finger protein 20-like 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20201022 MGI 1551707 Ptpre protein tyrosine phosphatase receptor type E gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:10921884 1551707 Ptpre protein tyrosine phosphatase receptor type E gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:14528021 1551707 Ptpre protein tyrosine phosphatase receptor type E gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:10921884 1551707 Ptpre protein tyrosine phosphatase receptor type E gene MP:0004357 long tibia IAGP N RGD:5509061 20141003 MGI PMID:14528021 1551707 Ptpre protein tyrosine phosphatase receptor type E gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:14528021 1551707 Ptpre protein tyrosine phosphatase receptor type E gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:14528021 1551707 Ptpre protein tyrosine phosphatase receptor type E gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:14528021 1551707 Ptpre protein tyrosine phosphatase receptor type E gene MP:0031073 decreased circulating type I collagen C-terminal telopeptide level IAGP N RGD:5509061 20200618 MGI PMID:14528021 1551708 Abtb2 ankyrin repeat and BTB domain containing 2 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20150430 MGI 1551708 Abtb2 ankyrin repeat and BTB domain containing 2 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20200402 MGI PMID:19393728 1551708 Abtb2 ankyrin repeat and BTB domain containing 2 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20200402 MGI PMID:25568138 1551708 Abtb2 ankyrin repeat and BTB domain containing 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1551708 Abtb2 ankyrin repeat and BTB domain containing 2 gene MP:0020148 abnormal susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200402 MGI PMID:19393728 1551708 Abtb2 ankyrin repeat and BTB domain containing 2 gene MP:0020148 abnormal susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200402 MGI PMID:25568138 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11640934 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12805218 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12925882 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9603515 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20221103 MGI 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11640934 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:9384379 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12925882 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9603515 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0001746 abnormal pituitary secretion IAGP N RGD:5509061 20141003 MGI PMID:9603515 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:9384379 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17030618 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12805218 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0002798 abnormal active avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:9384379 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0002802 abnormal discrimination learning IAGP N RGD:5509061 20141003 MGI PMID:11640934 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:9384379 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0002969 impaired social transmission of food preference IAGP N RGD:5509061 20141003 MGI PMID:11640934 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:15029245 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:12925882 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:9603515 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:12740578 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:12805218 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:11753386 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:12740578 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:16314537 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:17030618 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20221103 MGI 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:9603515 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:9603515 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12805218 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17030618 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:12805218 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:9384379 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:16314537 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:12805218 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:9384379 1551710 Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12805218 1551711 Or6b9 olfactory receptor family 6 subfamily B member 9 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:15186781 1551711 Or6b9 olfactory receptor family 6 subfamily B member 9 gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15186781 1551712 Tspan12 tetraspanin 12 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20200310 MGI PMID:19837033 1551712 Tspan12 tetraspanin 12 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20200310 MGI PMID:19837033 1551712 Tspan12 tetraspanin 12 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:19837033 1551712 Tspan12 tetraspanin 12 gene MP:0004368 abnormal stria vascularis vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:19837033 1551712 Tspan12 tetraspanin 12 gene MP:0006185 retina hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:19837033 1551712 Tspan12 tetraspanin 12 gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20200310 MGI PMID:19837033 1551712 Tspan12 tetraspanin 12 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200310 MGI PMID:19837033 1551712 Tspan12 tetraspanin 12 gene MP:0009392 retina gliosis IAGP N RGD:5509061 20200310 MGI PMID:19837033 1551712 Tspan12 tetraspanin 12 gene MP:0010452 retina microaneurysm IAGP N RGD:5509061 20200310 MGI PMID:19837033 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0000263 absent organized vascular network IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9683559 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:9683559 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19910638 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20223757 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23918385 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:8846781 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:7596437 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20223757 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19910638 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20223757 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7596437 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8846781 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:7596437 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20223757 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:7596437 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:9683559 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:9683559 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:9683559 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:7596437 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0003542 abnormal vascular endothelial cell development IAGP N RGD:5509061 20141003 MGI PMID:9683559 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20141003 MGI PMID:20223757 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:7596437 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:7596437 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:9683559 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0004106 lymphatic vessel hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20223757 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:20223757 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:9683559 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7596437 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19910638 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20223757 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7596437 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20223757 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8846781 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20223757 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7596437 1551713 Tie1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:10498691 1551714 Impdh1 inosine monophosphate dehydrogenase 1 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12944494 1551714 Impdh1 inosine monophosphate dehydrogenase 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12944494 1551714 Impdh1 inosine monophosphate dehydrogenase 1 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12944494 1551714 Impdh1 inosine monophosphate dehydrogenase 1 gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:12944494 1551714 Impdh1 inosine monophosphate dehydrogenase 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12944494 1551714 Impdh1 inosine monophosphate dehydrogenase 1 gene MP:0008515 thin retina outer nuclear layer IEA N RGD:5509061 20180215 MGI 1551714 Impdh1 inosine monophosphate dehydrogenase 1 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:12944494 1551714 Impdh1 inosine monophosphate dehydrogenase 1 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12944494 1551714 Impdh1 inosine monophosphate dehydrogenase 1 gene MP:0010235 abnormal retina inner limiting membrane morphology IEA N RGD:5509061 20180215 MGI 1551714 Impdh1 inosine monophosphate dehydrogenase 1 gene MP:0010236 abnormal retina outer limiting membrane morphology IEA N RGD:5509061 20180215 MGI 1551714 Impdh1 inosine monophosphate dehydrogenase 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20180215 MGI 1551715 Foxd1 forkhead box D1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20150625 MGI PMID:24732380 1551715 Foxd1 forkhead box D1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0002990 short ureter IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0003605 fused kidneys IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20200206 MGI PMID:30830875 1551715 Foxd1 forkhead box D1 gene MP:0005426 tachypnea IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20200206 MGI PMID:30830875 1551715 Foxd1 forkhead box D1 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0010987 abnormal nephrogenic mesenchyme morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551715 Foxd1 forkhead box D1 gene MP:0011361 pelvic kidney IAGP N RGD:5509061 20141003 MGI PMID:8666231 1551716 Fxn frataxin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:15028670 1551716 Fxn frataxin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:10767347 1551716 Fxn frataxin gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:10767347 1551716 Fxn frataxin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0001847 brain inflammation IAGP N RGD:5509061 20200310 MGI PMID:25104852 1551716 Fxn frataxin gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:11852098 1551716 Fxn frataxin gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:15028670 1551716 Fxn frataxin gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:10767347 1551716 Fxn frataxin gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20200310 MGI PMID:15028670 1551716 Fxn frataxin gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:15028670 1551716 Fxn frataxin gene MP:0002883 chromatolysis IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0002899 fatigue IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20240523 MGI PMID:32586831 1551716 Fxn frataxin gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200310 MGI PMID:11852098 1551716 Fxn frataxin gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20200310 MGI PMID:15028670 1551716 Fxn frataxin gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20200310 MGI PMID:15028670 1551716 Fxn frataxin gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20231109 MGI PMID:15028670 1551716 Fxn frataxin gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20200310 MGI 1551716 Fxn frataxin gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0005330 cardiomyopathy IEA N RGD:5509061 20200310 MGI 1551716 Fxn frataxin gene MP:0005333 decreased heart rate IEA N RGD:5509061 20200310 MGI 1551716 Fxn frataxin gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:15028670 1551716 Fxn frataxin gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20200310 MGI PMID:15028670 1551716 Fxn frataxin gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20240523 MGI PMID:32586831 1551716 Fxn frataxin gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0006404 abnormal lumbar dorsal root ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20240523 MGI PMID:32586831 1551716 Fxn frataxin gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20240523 MGI PMID:32586831 1551716 Fxn frataxin gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20200310 MGI PMID:15028670 1551716 Fxn frataxin gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20200310 MGI PMID:15028670 1551716 Fxn frataxin gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10767347 1551716 Fxn frataxin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551716 Fxn frataxin gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20240523 MGI PMID:32586831 1551716 Fxn frataxin gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20240523 MGI PMID:32586831 1551716 Fxn frataxin gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20240523 MGI PMID:32586831 1551716 Fxn frataxin gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0011638 abnormal mitochondrial chromosome morphology IAGP N RGD:5509061 20240523 MGI PMID:32586831 1551716 Fxn frataxin gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20240523 MGI PMID:32586831 1551716 Fxn frataxin gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20200310 MGI PMID:10767347 1551716 Fxn frataxin gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551716 Fxn frataxin gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:10767347 1551716 Fxn frataxin gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0020367 increased heart iron level IAGP N RGD:5509061 20200310 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0020367 increased heart iron level IAGP N RGD:5509061 20200310 MGI PMID:11852098 1551716 Fxn frataxin gene MP:0020367 increased heart iron level IAGP N RGD:5509061 20200310 MGI PMID:15028670 1551716 Fxn frataxin gene MP:0020367 increased heart iron level IAGP N RGD:5509061 20200310 MGI PMID:16919418 1551716 Fxn frataxin gene MP:0020423 abnormal mitochondrial biogenesis IAGP N RGD:5509061 20200310 MGI PMID:28444186 1551716 Fxn frataxin gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:11175786 1551716 Fxn frataxin gene MP:0021161 increased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:15028670 1551718 Tomm70a translocase of outer mitochondrial membrane 70A gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20240919 MGI 1551718 Tomm70a translocase of outer mitochondrial membrane 70A gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20240919 MGI 1551718 Tomm70a translocase of outer mitochondrial membrane 70A gene MP:0001698 decreased embryo size IEA N RGD:5509061 20240919 MGI 1551718 Tomm70a translocase of outer mitochondrial membrane 70A gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20240919 MGI 1551718 Tomm70a translocase of outer mitochondrial membrane 70A gene MP:0009331 absent primitive node IEA N RGD:5509061 20240919 MGI 1551718 Tomm70a translocase of outer mitochondrial membrane 70A gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1551718 Tomm70a translocase of outer mitochondrial membrane 70A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551718 Tomm70a translocase of outer mitochondrial membrane 70A gene MP:0012724 absent head fold IEA N RGD:5509061 20240919 MGI 1551718 Tomm70a translocase of outer mitochondrial membrane 70A gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 1551721 Tmem45a transmembrane protein 45a gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1551721 Tmem45a transmembrane protein 45a gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1551721 Tmem45a transmembrane protein 45a gene MP:0000692 small spleen IEA N RGD:5509061 20201022 MGI 1551721 Tmem45a transmembrane protein 45a gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1551721 Tmem45a transmembrane protein 45a gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1551721 Tmem45a transmembrane protein 45a gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24239381 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20240229 MGI PMID:25476608 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0000411 shiny fur IAGP N RGD:5509061 20141003 MGI PMID:6863898 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:24239381 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:3955134 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001147 small testis IAGP N RGD:5509061 20240229 MGI PMID:25476608 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:14757819 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:6863898 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:6863898 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:24239381 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20240229 MGI PMID:25476608 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:24239381 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:3955134 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:24239381 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:3955134 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:6863898 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001925 male infertility IAGP N RGD:5509061 20240229 MGI PMID:25476608 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:3955134 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20200514 MGI 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20240229 MGI PMID:25476608 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:3955134 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:6863898 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:24239381 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0003686 abnormal eye muscle morphology IAGP N RGD:5509061 20240229 MGI PMID:25476608 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:3955134 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:24239381 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:3955134 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:3955134 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20141003 MGI PMID:24239381 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20141003 MGI PMID:3955134 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20141003 MGI PMID:24239381 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20240229 MGI PMID:25476608 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:3955134 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20240229 MGI PMID:25476608 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20240229 MGI PMID:25476608 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20141003 MGI PMID:24239381 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24239381 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20191226 MGI PMID:3955134 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0031345 developmental cataract IAGP N RGD:5509061 20220217 MGI PMID:6863898 1551722 Tbc1d20 TBC1 domain family, member 20 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20240229 MGI PMID:25476608 1551723 Bola3 bolA family member 3 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20210520 MGI PMID:32313871 1551723 Bola3 bolA family member 3 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20210520 MGI PMID:32313871 1551723 Bola3 bolA family member 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210520 MGI PMID:32313871 1551723 Bola3 bolA family member 3 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20210520 MGI PMID:32313871 1551723 Bola3 bolA family member 3 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20210520 MGI PMID:32313871 1551723 Bola3 bolA family member 3 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20210520 MGI PMID:32313871 1551723 Bola3 bolA family member 3 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20210520 MGI PMID:32313871 1551723 Bola3 bolA family member 3 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20210520 MGI PMID:32313871 1551723 Bola3 bolA family member 3 gene MP:0014145 increased white adipose tissue mass IAGP N RGD:5509061 20210520 MGI PMID:32313871 1551723 Bola3 bolA family member 3 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20210520 MGI PMID:32313871 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8598041 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9256469 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:11602620 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:11937578 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:8638109 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8598041 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9256469 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9551884 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11290790 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11290790 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12646641 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8598040 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8638109 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9256469 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:11602620 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:11937578 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:10843678 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:8638109 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9551884 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0005041 abnormal antigen presentation via MHC class II IAGP N RGD:5509061 20141003 MGI PMID:11290790 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0005041 abnormal antigen presentation via MHC class II IAGP N RGD:5509061 20141003 MGI PMID:12646641 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0005041 abnormal antigen presentation via MHC class II IAGP N RGD:5509061 20141003 MGI PMID:15034026 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0005041 abnormal antigen presentation via MHC class II IAGP N RGD:5509061 20141003 MGI PMID:8598041 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:9551884 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0005043 defective assembly of class II molecules IAGP N RGD:5509061 20141003 MGI PMID:11290790 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12646641 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8598041 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8638109 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:11937578 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11937578 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11290790 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15034026 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8598041 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8638109 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9256469 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9551884 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9256469 1551725 H2-DMa histocompatibility 2, class II, locus DMa gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9551884 1551726 Etfdh electron transferring flavoprotein, dehydrogenase gene MP:0000751 myopathy IAGP N RGD:5509061 20240404 MGI PMID:38243131 1551726 Etfdh electron transferring flavoprotein, dehydrogenase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240404 MGI PMID:38243131 1551726 Etfdh electron transferring flavoprotein, dehydrogenase gene MP:0001263 weight loss IAGP N RGD:5509061 20240404 MGI PMID:38243131 1551726 Etfdh electron transferring flavoprotein, dehydrogenase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20220811 MGI 1551726 Etfdh electron transferring flavoprotein, dehydrogenase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20240404 MGI PMID:38243131 1551726 Etfdh electron transferring flavoprotein, dehydrogenase gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20240404 MGI PMID:38243131 1551726 Etfdh electron transferring flavoprotein, dehydrogenase gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20240404 MGI PMID:38243131 1551726 Etfdh electron transferring flavoprotein, dehydrogenase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551726 Etfdh electron transferring flavoprotein, dehydrogenase gene MP:0014344 abnormal skeletal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240404 MGI PMID:38243131 1551728 Zfp251 zinc finger protein 251 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20231026 MGI PMID:36565788 1551728 Zfp251 zinc finger protein 251 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20231026 MGI PMID:36565788 1551728 Zfp251 zinc finger protein 251 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20231026 MGI PMID:36565788 1551728 Zfp251 zinc finger protein 251 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20231026 MGI PMID:36565788 1551728 Zfp251 zinc finger protein 251 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20231026 MGI PMID:36565788 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:31276560 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20200310 MGI PMID:31276560 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20200310 MGI PMID:31276560 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20200310 MGI 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:31276560 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:31276560 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:31276560 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0003064 decreased coping response IEA N RGD:5509061 20210128 MGI 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0003087 absent allantois IAGP N RGD:5509061 20200310 MGI PMID:31276560 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20200310 MGI PMID:31276560 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:31276560 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20200310 MGI 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20200310 MGI PMID:31276560 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20200310 MGI PMID:31276560 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0011192 decreased embryonic epiblast cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:31276560 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0011388 absent heart IAGP N RGD:5509061 20200310 MGI PMID:31276560 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0012724 absent head fold IAGP N RGD:5509061 20200310 MGI PMID:31276560 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1551730 Elof1 ELF1 homolog, elongation factor 1 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20240620 MGI PMID:31276560 1551735 Lhx9 LIM homeobox protein 9 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150416 MGI PMID:25112520 1551735 Lhx9 LIM homeobox protein 9 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0001926 female infertility IAGP N RGD:5509061 20150416 MGI PMID:25112520 1551735 Lhx9 LIM homeobox protein 9 gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0003578 absent ovary IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0004894 uterus atrophy IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0004895 vagina atrophy IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0005644 agonadal IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0005652 sex reversal IAGP N RGD:5509061 20150416 MGI PMID:25112520 1551735 Lhx9 LIM homeobox protein 9 gene MP:0006415 absent testes IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:10706291 1551735 Lhx9 LIM homeobox protein 9 gene MP:0021092 abnormal dorsal interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:18701067 1551735 Lhx9 LIM homeobox protein 9 gene MP:0030934 decreased primordial germ cell proliferation IAGP N RGD:5509061 20190411 MGI PMID:10706291 1551746 Arl10 ADP-ribosylation factor-like 10 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1551746 Arl10 ADP-ribosylation factor-like 10 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20150430 MGI 1551746 Arl10 ADP-ribosylation factor-like 10 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000018 small ears IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000018 small ears IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000022 abnormal ear shape IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20180201 MGI PMID:24700590 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20180201 MGI PMID:12514106 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20180201 MGI PMID:16221728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20180201 MGI PMID:19185569 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20180201 MGI PMID:15037550 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000040 absent middle ear ossicles IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000073 absent craniofacial bones IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000073 absent craniofacial bones IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000087 absent mandible IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000087 absent mandible IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000087 absent mandible IAGP N RGD:5509061 20180201 MGI PMID:22190459 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20180201 MGI PMID:17376812 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20180201 MGI PMID:18501887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20180201 MGI PMID:19185569 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20180201 MGI PMID:23546880 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20180201 MGI PMID:24700590 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20180201 MGI PMID:24895408 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20221117 MGI PMID:29986157 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20221124 MGI PMID:31526805 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20180201 MGI PMID:17610273 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000094 absent alveolar process IAGP N RGD:5509061 20180201 MGI PMID:17610273 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20180201 MGI PMID:22156581 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20180201 MGI PMID:23546880 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000099 absent vomer bone IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000100 abnormal ethmoid bone morphology IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:12490557 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20221020 MGI PMID:17927973 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:12490557 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20180201 MGI PMID:12490557 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20180201 MGI PMID:26341559 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20200917 MGI PMID:31733190 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:12514106 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:15037550 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:17376812 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:17499702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:18483623 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:21982646 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:22745308 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:24895408 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:26341559 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20190822 MGI PMID:31232685 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20191114 MGI PMID:25451153 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221006 MGI PMID:35212626 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221020 MGI PMID:33772547 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230504 MGI PMID:26746790 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230629 MGI PMID:28408410 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20221006 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20221006 MGI PMID:35151207 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20180201 MGI PMID:17610273 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20221201 MGI PMID:24433583 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20180201 MGI PMID:22156581 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000128 growth retardation of molars IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000161 scoliosis IAGP N RGD:5509061 20220616 MGI PMID:28829946 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20180201 MGI PMID:21098571 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20180201 MGI PMID:18188448 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231109 MGI PMID:36745292 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20180201 MGI PMID:18501887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20180201 MGI PMID:19008477 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20180201 MGI PMID:16557299 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231109 MGI PMID:36745292 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20180201 MGI PMID:17172441 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000373 belly spot IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000373 belly spot IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000373 belly spot IAGP N RGD:5509061 20181122 MGI PMID:25818501 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000373 belly spot IAGP N RGD:5509061 20181227 MGI PMID:27001213 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180201 MGI PMID:18483623 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180201 MGI PMID:19185569 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180201 MGI PMID:19805360 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180201 MGI PMID:21098571 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180201 MGI PMID:22190459 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180201 MGI PMID:22991437 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180201 MGI PMID:23454479 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180201 MGI PMID:23546880 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180201 MGI PMID:24497849 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20191114 MGI PMID:25451153 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20220922 MGI PMID:32169905 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20220922 MGI PMID:32169905 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20221117 MGI PMID:29986157 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000435 shortened head IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000435 shortened head IAGP N RGD:5509061 20221117 MGI PMID:29986157 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20180201 MGI PMID:24700590 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20180201 MGI PMID:17376812 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20230504 MGI PMID:26746790 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000445 short snout IAGP N RGD:5509061 20180201 MGI PMID:12490557 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000445 short snout IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000445 short snout IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000445 short snout IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000445 short snout IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000445 short snout IAGP N RGD:5509061 20180201 MGI PMID:19047372 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000445 short snout IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000445 short snout IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000445 short snout IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20180201 MGI PMID:24700590 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20221124 MGI PMID:31526805 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:24700590 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20180201 MGI PMID:19185569 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20180201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20221124 MGI PMID:31526805 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:24700590 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20191003 MGI PMID:30842416 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20180201 MGI PMID:12469121 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20180201 MGI PMID:12469121 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000678 abnormal parathyroid gland morphology IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20180201 MGI PMID:26061883 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000692 small spleen IAGP N RGD:5509061 20180201 MGI PMID:26061883 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20180201 MGI PMID:26061883 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20180201 MGI PMID:17499702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20180201 MGI PMID:19008477 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20180201 MGI PMID:21098571 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000705 athymia IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000705 athymia IAGP N RGD:5509061 20180201 MGI PMID:21098571 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20180201 MGI PMID:12490557 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20180201 MGI PMID:17652354 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000746 weakness IAGP N RGD:5509061 20180201 MGI PMID:17553423 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000753 paralysis IAGP N RGD:5509061 20180201 MGI PMID:15198977 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20180201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000771 abnormal brain size IAGP N RGD:5509061 20180201 MGI PMID:17172441 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000836 abnormal substantia nigra morphology IAGP N RGD:5509061 20180201 MGI PMID:15987955 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20180201 MGI PMID:20614471 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20180201 MGI PMID:20614471 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20180201 MGI PMID:17166916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20180201 MGI PMID:17693261 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20180201 MGI PMID:12682014 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20180201 MGI PMID:22190459 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20180201 MGI PMID:12682014 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20180201 MGI PMID:21502507 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20180201 MGI PMID:22190459 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000906 abnormal trigeminal V mesencephalic nucleus morphology IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20180201 MGI PMID:16221970 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20180201 MGI PMID:18440989 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20180201 MGI PMID:21502507 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20180201 MGI PMID:20220021 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20180201 MGI PMID:20220021 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20180201 MGI PMID:16267821 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20180201 MGI PMID:22190459 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20180201 MGI PMID:19421194 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20180201 MGI PMID:15198977 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20180201 MGI PMID:19421194 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20180201 MGI PMID:18849985 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20180201 MGI PMID:21098571 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20180201 MGI PMID:24173031 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20180201 MGI PMID:17553423 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20180201 MGI PMID:19805360 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20180201 MGI PMID:24173031 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20180201 MGI PMID:18849985 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20180201 MGI PMID:19805360 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20180201 MGI PMID:24173031 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20180201 MGI PMID:26418744 1551747 H2az2 H2A.Z histone variant 2 gene MP:0000969 abnormal nociceptor morphology IAGP N RGD:5509061 20180201 MGI PMID:26418744 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20180201 MGI PMID:12469121 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20180201 MGI PMID:18501887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20180201 MGI PMID:21098571 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20180201 MGI PMID:24173031 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001026 abnormal adrenergic neuron morphology IAGP N RGD:5509061 20180201 MGI PMID:17531968 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001034 abnormal parasympathetic ganglion morphology IAGP N RGD:5509061 20180201 MGI PMID:20133851 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20180201 MGI PMID:17075884 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20180201 MGI PMID:17075884 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20180201 MGI PMID:17075884 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20180201 MGI PMID:17553423 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001062 absent oculomotor nerve IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20180201 MGI PMID:15198977 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20180201 MGI PMID:20133851 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20180201 MGI PMID:23055936 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20180201 MGI PMID:18440989 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20180201 MGI PMID:18849985 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20180201 MGI PMID:23055936 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20180201 MGI PMID:18440989 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20180201 MGI PMID:23055936 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20180201 MGI PMID:18440989 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20180201 MGI PMID:18440989 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20180201 MGI PMID:19805360 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001109 absent Schwann cell precursors IAGP N RGD:5509061 20180201 MGI PMID:19805360 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001212 skin lesions IAGP N RGD:5509061 20180201 MGI PMID:20346763 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001255 decreased body height IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20181227 MGI PMID:27001213 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191003 MGI PMID:30842416 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:12469121 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:17693261 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:22156581 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20231109 MGI PMID:36745292 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20180201 MGI PMID:17553423 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20180201 MGI PMID:18693272 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20180201 MGI PMID:16203745 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20180201 MGI PMID:16207763 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20180201 MGI PMID:16203745 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20180201 MGI PMID:20568247 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20191114 MGI PMID:25451153 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20180201 MGI PMID:24700590 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001306 small lens IAGP N RGD:5509061 20180201 MGI PMID:17428831 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20180201 MGI PMID:22503753 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20180201 MGI PMID:20568247 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20180201 MGI PMID:20568247 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20180201 MGI PMID:16203745 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20180201 MGI PMID:16203745 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20180201 MGI PMID:18483623 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001341 absent eyelids IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20180201 MGI PMID:22745308 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20180201 MGI PMID:23134367 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20180201 MGI PMID:23134367 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20220616 MGI PMID:28829946 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180201 MGI PMID:15987955 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180201 MGI PMID:23792428 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20180201 MGI PMID:23792428 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20220616 MGI PMID:28829946 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001412 excessive scratching IAGP N RGD:5509061 20180201 MGI PMID:20346763 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20180201 MGI PMID:22156581 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001438 aphagia IAGP N RGD:5509061 20180201 MGI PMID:17610273 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20180201 MGI PMID:23134367 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20180201 MGI PMID:23134367 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001490 abnormal vibrissae reflex IAGP N RGD:5509061 20180201 MGI PMID:15198977 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20180201 MGI PMID:15987955 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20180201 MGI PMID:21413144 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20180201 MGI PMID:17693261 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20180201 MGI PMID:17693261 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20180201 MGI PMID:17172441 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20180201 MGI PMID:17499702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20180201 MGI PMID:18188448 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20180201 MGI PMID:20045680 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20180201 MGI PMID:17172441 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20180201 MGI PMID:22156581 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20180201 MGI PMID:12490557 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180201 MGI PMID:18501887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001785 edema IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20180201 MGI PMID:26061883 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:17499702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001890 anencephaly IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20180201 MGI PMID:12490557 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20180201 MGI PMID:19605684 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20180201 MGI PMID:12469121 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20180201 MGI PMID:20045680 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001957 apnea IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20180201 MGI PMID:15198977 1551747 H2az2 H2A.Z histone variant 2 gene MP:0001993 abnormal blinking IAGP N RGD:5509061 20180201 MGI PMID:15198977 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20180201 MGI PMID:12469121 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20180201 MGI PMID:23281395 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20180201 MGI PMID:12469121 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20180201 MGI PMID:12682014 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20180201 MGI PMID:20614471 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20180201 MGI PMID:26418744 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20180201 MGI PMID:12490557 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:18693272 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:22156581 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:23571217 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002083 premature death IAGP N RGD:5509061 20181227 MGI PMID:27001213 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002083 premature death IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002083 premature death IAGP N RGD:5509061 20231109 MGI PMID:36745292 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20180201 MGI PMID:12514106 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20180201 MGI PMID:16221728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20180201 MGI PMID:18501887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20180201 MGI PMID:19185569 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20180201 MGI PMID:22190459 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20190822 MGI PMID:31232685 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20230504 MGI PMID:26746790 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20180201 MGI PMID:16557299 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20180201 MGI PMID:17531968 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20180201 MGI PMID:20614471 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20180201 MGI PMID:22190459 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180201 MGI PMID:21502507 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180201 MGI PMID:22991437 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200917 MGI PMID:31733190 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:16703618 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:17376812 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:19605684 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:19855134 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:23184148 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:23303524 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26341559 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002183 gliosis IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20180201 MGI PMID:23591430 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20180201 MGI PMID:19008477 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20180201 MGI PMID:17344228 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002244 abnormal turbinate morphology IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002251 abnormal nasopharynx morphology IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:12490557 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:16332365 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:16557299 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:17172441 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:17344228 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:17499702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:21098571 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20180201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20221006 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20221124 MGI PMID:31526805 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20180201 MGI PMID:21413144 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002735 abnormal chemical nociception IAGP N RGD:5509061 20180201 MGI PMID:20346763 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:19805360 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20180201 MGI PMID:17553423 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20180201 MGI PMID:20220021 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20180201 MGI PMID:24210822 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20180201 MGI PMID:17553423 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20180201 MGI PMID:18693272 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002938 white spotting IAGP N RGD:5509061 20180201 MGI PMID:18693272 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002940 variable body spotting IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20180201 MGI PMID:20498049 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20180201 MGI PMID:20045680 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20180201 MGI PMID:16221728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20180201 MGI PMID:19008477 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20180201 MGI PMID:16203745 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:18188448 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003142 anotia IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003154 abnormal soft palate morphology IAGP N RGD:5509061 20221006 MGI PMID:35212626 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20180201 MGI PMID:23454479 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20180201 MGI PMID:24173031 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20180201 MGI PMID:12514106 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20180201 MGI PMID:20568247 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20180201 MGI PMID:26061883 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003359 hypaxial muscle hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:20045680 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20231109 MGI PMID:36745292 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003416 premature bone ossification IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003418 premature intramembranous bone ossification IAGP N RGD:5509061 20180201 MGI PMID:19047372 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20180201 MGI PMID:22190459 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003494 parathyroid hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:19008477 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20180201 MGI PMID:24173031 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20180201 MGI PMID:19805360 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20180201 MGI PMID:23454479 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20210603 MGI PMID:32414840 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20180201 MGI PMID:24173031 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20180201 MGI PMID:18483623 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20180201 MGI PMID:22156581 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20220922 MGI PMID:32169905 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003760 decreased palatal length IAGP N RGD:5509061 20180201 MGI PMID:22156581 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003773 eclabion IAGP N RGD:5509061 20180201 MGI PMID:24700590 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003792 abnormal major salivary gland morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20180201 MGI PMID:24173031 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003818 abnormal eye muscle development IAGP N RGD:5509061 20180201 MGI PMID:16203745 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003834 abnormal adrenergic chromaffin cell morphology IAGP N RGD:5509061 20180201 MGI PMID:12469121 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003840 abnormal coronal suture morphology IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20180201 MGI PMID:21502507 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20180201 MGI PMID:23134367 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20180201 MGI PMID:24700590 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20180201 MGI PMID:26418744 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20191114 MGI PMID:25451153 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20180201 MGI PMID:18440989 1551747 H2az2 H2A.Z histone variant 2 gene MP:0003994 abnormal dorsal spinal root morphology IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20180201 MGI PMID:17553423 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20180201 MGI PMID:17172441 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20180201 MGI PMID:23792428 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004075 decreased Schwann cell precursor number IAGP N RGD:5509061 20180201 MGI PMID:19805360 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004096 abnormal midbrain-hindbrain boundary development IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20180201 MGI PMID:17344228 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20180201 MGI PMID:16332365 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20180201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20220922 MGI PMID:32169905 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20180201 MGI PMID:16557299 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20180201 MGI PMID:17172441 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20180201 MGI PMID:19008477 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20180201 MGI PMID:16332365 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20180201 MGI PMID:16557299 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20180201 MGI PMID:17499702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20180201 MGI PMID:19008477 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20180201 MGI PMID:24173031 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004204 absent stapes IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004204 absent stapes IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004204 absent stapes IAGP N RGD:5509061 20180201 MGI PMID:16221728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20180201 MGI PMID:16203745 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004283 absent cornea endothelium IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004318 absent incus IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004318 absent incus IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004318 absent incus IAGP N RGD:5509061 20180201 MGI PMID:19185569 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004319 absent malleus IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004319 absent malleus IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004319 absent malleus IAGP N RGD:5509061 20180201 MGI PMID:19185569 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004378 frontal bone foramen IAGP N RGD:5509061 20180201 MGI PMID:17376812 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004378 frontal bone foramen IAGP N RGD:5509061 20180201 MGI PMID:19605684 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004379 wide frontal bone IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004380 short frontal bone IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004380 short frontal bone IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004380 short frontal bone IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004380 short frontal bone IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004385 interparietal bone hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004420 parietal bone hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20180201 MGI PMID:12514106 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004424 temporal bone hypoplasia IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004424 temporal bone hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004424 temporal bone hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20180201 MGI PMID:19185569 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004444 small supraoccipital bone IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004447 small basioccipital bone IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004450 presphenoid bone hypoplasia IAGP N RGD:5509061 20230504 MGI PMID:26746790 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004451 short presphenoid bone IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20221020 MGI PMID:17927973 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20180201 MGI PMID:12514106 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004454 absent pterygoid process IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004455 pterygoid bone hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004458 absent alisphenoid bone IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004459 small alisphenoid bone IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004459 small alisphenoid bone IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004461 basisphenoid bone hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20230504 MGI PMID:26746790 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004468 small zygomatic bone IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004468 small zygomatic bone IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20180201 MGI PMID:24895408 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20180201 MGI PMID:24895408 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004472 broad nasal bone IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004474 enlarged nasal bone IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004537 abnormal palatine bone horizontal plate morphology IAGP N RGD:5509061 20180201 MGI PMID:17610273 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20180201 MGI PMID:17610273 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004539 absent maxilla IAGP N RGD:5509061 20180201 MGI PMID:22190459 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004539 absent maxilla IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004540 small maxilla IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004540 small maxilla IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004540 small maxilla IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004592 small mandible IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004592 small mandible IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004592 small mandible IAGP N RGD:5509061 20180201 MGI PMID:24700590 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004592 small mandible IAGP N RGD:5509061 20180201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004592 small mandible IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004592 small mandible IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004592 small mandible IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004592 small mandible IAGP N RGD:5509061 20221117 MGI PMID:29986157 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004592 small mandible IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004594 abnormal mandibular coronoid process morphology IAGP N RGD:5509061 20180201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004595 abnormal mandibular condyloid process morphology IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004595 abnormal mandibular condyloid process morphology IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20180201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20180201 MGI PMID:12490557 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20180201 MGI PMID:16332365 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004791 absent lower incisors IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20210603 MGI PMID:32414840 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004830 short incisors IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004870 small premaxilla IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004870 small premaxilla IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20230504 MGI PMID:26746790 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004899 absent temporal bone squamous part IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004911 absent mandibular condyloid process IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004911 absent mandibular condyloid process IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004911 absent mandibular condyloid process IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004911 absent mandibular condyloid process IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20180201 MGI PMID:17610273 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004913 absent mandibular angle IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004913 absent mandibular angle IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004913 absent mandibular angle IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004913 absent mandibular angle IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004916 absent Reichert cartilage IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20180201 MGI PMID:23134367 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20180201 MGI PMID:26061883 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20180201 MGI PMID:21502507 1551747 H2az2 H2A.Z histone variant 2 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180201 MGI PMID:26061883 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20181220 MGI PMID:21610032 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20180201 MGI PMID:16203745 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20191114 MGI PMID:25451153 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20180201 MGI PMID:12514106 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20180201 MGI PMID:12514106 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20180201 MGI PMID:16221728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20180201 MGI PMID:19185569 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20180201 MGI PMID:19185569 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20190822 MGI PMID:31232685 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20221006 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005174 abnormal tail pigmentation IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20191114 MGI PMID:25451153 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005198 abnormal aqueous drainage system morphology IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005203 abnormal trabecular meshwork morphology IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005204 abnormal canal of Schlemm morphology IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005262 coloboma IAGP N RGD:5509061 20191114 MGI PMID:25451153 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20180201 MGI PMID:20568247 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005314 absent thyroid gland IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20180201 MGI PMID:17531968 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005352 small cranium IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005352 small cranium IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005352 small cranium IAGP N RGD:5509061 20230629 MGI PMID:28408410 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20180201 MGI PMID:19185569 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005359 growth retardation of incisors IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20180201 MGI PMID:26418744 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20210603 MGI PMID:32414840 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005451 abnormal body composition IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005497 optic nerve cupping IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20180201 MGI PMID:20568247 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20191114 MGI PMID:25451153 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20180201 MGI PMID:16221728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20180201 MGI PMID:16221728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20180201 MGI PMID:17376812 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20180201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20221124 MGI PMID:31526805 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20180201 MGI PMID:18188448 1551747 H2az2 H2A.Z histone variant 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20221006 MGI PMID:35212626 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20180201 MGI PMID:12514106 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20180201 MGI PMID:17172441 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006101 absent tegmentum IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006105 small tectum IAGP N RGD:5509061 20180201 MGI PMID:17166916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006106 absent tectum IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006111 abnormal coronary circulation IAGP N RGD:5509061 20231109 MGI PMID:36745292 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20180201 MGI PMID:15789410 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20180201 MGI PMID:17172441 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20180201 MGI PMID:17344228 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20180201 MGI PMID:21597012 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006198 enophthalmos IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20180201 MGI PMID:23408898 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006211 small orbits IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20191114 MGI PMID:25451153 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006230 iris stroma hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:20568247 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006306 abnormal nasal pit morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006306 abnormal nasal pit morphology IAGP N RGD:5509061 20230309 MGI PMID:23872235 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006322 abnormal perichondrium morphology IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006326 conductive hearing impairment IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20180201 MGI PMID:21098571 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006338 abnormal second pharyngeal arch morphology IAGP N RGD:5509061 20180201 MGI PMID:12514106 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20180201 MGI PMID:22190459 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20180201 MGI PMID:16332365 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20180201 MGI PMID:19855134 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006400 decreased molar number IAGP N RGD:5509061 20221201 MGI PMID:24433583 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006408 dorsal root ganglion hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:18849985 1551747 H2az2 H2A.Z histone variant 2 gene MP:0006411 upturned snout IAGP N RGD:5509061 20180201 MGI PMID:24700590 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008052 abnormal serous gland morphology IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20180201 MGI PMID:26061883 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20180201 MGI PMID:26061883 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20180201 MGI PMID:26061883 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008259 abnormal optic disk morphology IAGP N RGD:5509061 20190411 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20230504 MGI PMID:26746790 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20180201 MGI PMID:19047372 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20220922 MGI PMID:32169905 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008276 failure of intramembranous bone ossification IAGP N RGD:5509061 20180201 MGI PMID:19605684 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20180201 MGI PMID:12469121 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008302 thin adrenal cortex IAGP N RGD:5509061 20180201 MGI PMID:12469121 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008372 small malleus IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008375 short malleus manubrium IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008375 short malleus manubrium IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008376 small malleus manubrium IAGP N RGD:5509061 20180201 MGI PMID:17523175 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008380 abnormal gonial bone morphology IAGP N RGD:5509061 20180201 MGI PMID:16221728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008380 abnormal gonial bone morphology IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008381 absent gonial bone IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008384 absent nasal capsule IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008384 absent nasal capsule IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008384 absent nasal capsule IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008384 absent nasal capsule IAGP N RGD:5509061 20200917 MGI PMID:31733190 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008384 absent nasal capsule IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008385 absent basisphenoid bone IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008386 absent styloid process IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008386 absent styloid process IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008386 absent styloid process IAGP N RGD:5509061 20180201 MGI PMID:16221728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20180201 MGI PMID:17553423 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008467 absent proprioceptive neurons IAGP N RGD:5509061 20220616 MGI PMID:28829946 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20180201 MGI PMID:26061883 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20180201 MGI PMID:26061883 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008486 decreased muscle spindle number IAGP N RGD:5509061 20180201 MGI PMID:23792428 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180201 MGI PMID:18693272 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20180201 MGI PMID:19251646 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20180201 MGI PMID:23546880 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008532 decreased chemical nociceptive threshold IAGP N RGD:5509061 20180201 MGI PMID:18849985 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008534 enlarged fourth ventricle IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20180201 MGI PMID:24497849 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20180201 MGI PMID:18440989 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20181227 MGI PMID:27001213 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20200917 MGI PMID:31733190 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008797 facial cleft IAGP N RGD:5509061 20180201 MGI PMID:19185569 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008797 facial cleft IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008818 abnormal interfrontal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:19047372 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20180201 MGI PMID:26061883 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20180201 MGI PMID:22745308 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20180201 MGI PMID:20614471 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20180201 MGI PMID:21246653 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20180201 MGI PMID:24173031 1551747 H2az2 H2A.Z histone variant 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20180201 MGI PMID:24173031 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009025 abnormal brain dura mater morphology IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009039 absent inferior colliculus IAGP N RGD:5509061 20180201 MGI PMID:12682014 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009048 enlarged tectum IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20191114 MGI PMID:25451153 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009284 abnormal sympathetic neuron innervation pattern IAGP N RGD:5509061 20180201 MGI PMID:22343533 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009284 abnormal sympathetic neuron innervation pattern IAGP N RGD:5509061 20180201 MGI PMID:23454479 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009379 abnormal foot pigmentation IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009386 abnormal dermal melanocyte morphology IAGP N RGD:5509061 20181220 MGI PMID:21610032 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20181220 MGI PMID:21610032 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20180201 MGI PMID:19805360 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20180201 MGI PMID:24052814 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009483 enlarged ileum IAGP N RGD:5509061 20180201 MGI PMID:17553423 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20221020 MGI PMID:17927973 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20221117 MGI PMID:29986157 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20230504 MGI PMID:26746790 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009579 acephaly IAGP N RGD:5509061 20180201 MGI PMID:24895408 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20220922 MGI PMID:32169905 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20221006 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20221006 MGI PMID:35212626 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20221124 MGI PMID:31526805 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009654 abnormal primary palate development IAGP N RGD:5509061 20180201 MGI PMID:22156581 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20180201 MGI PMID:23546880 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221006 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221006 MGI PMID:35151207 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20230302 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20180201 MGI PMID:20045680 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009782 abnormal basicranium angle IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20181122 MGI PMID:25818501 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009798 abnormal ophthalmic nerve morphology IAGP N RGD:5509061 20180201 MGI PMID:24052814 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009844 abnormal neural crest cell apoptosis IAGP N RGD:5509061 20180201 MGI PMID:17344228 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009845 abnormal neural crest cell morphology IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009845 abnormal neural crest cell morphology IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009845 abnormal neural crest cell morphology IAGP N RGD:5509061 20180201 MGI PMID:18242513 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009859 eye opacity IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:23546880 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20221006 MGI PMID:35212626 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009884 palatal shelf fusion with tongue or mandible IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20220922 MGI PMID:32169905 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20221201 MGI PMID:24433583 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20180201 MGI PMID:15037550 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20180201 MGI PMID:17376812 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20180201 MGI PMID:17610273 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20180201 MGI PMID:23546880 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20180201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221006 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221124 MGI PMID:31526805 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221006 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221020 MGI PMID:17927973 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221020 MGI PMID:33772547 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221117 MGI PMID:29986157 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009889 persistence of medial edge epithelium during palatal shelf fusion IAGP N RGD:5509061 20221006 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20180201 MGI PMID:17610273 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20180201 MGI PMID:23546880 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20220922 MGI PMID:32169905 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221006 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221006 MGI PMID:35151207 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221020 MGI PMID:17927973 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221201 MGI PMID:24433583 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009891 abnormal palate bone morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009892 palate bone hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009893 cleft primary palate IAGP N RGD:5509061 20221006 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009894 absent hard palate IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009896 palatine bone horizontal plate hypoplasia IAGP N RGD:5509061 20221006 MGI PMID:35212626 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009896 palatine bone horizontal plate hypoplasia IAGP N RGD:5509061 20230504 MGI PMID:26746790 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009897 decreased maxillary shelf size IAGP N RGD:5509061 20221006 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009898 maxillary shelf hypoplasia IAGP N RGD:5509061 20221006 MGI PMID:35212626 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009898 maxillary shelf hypoplasia IAGP N RGD:5509061 20230504 MGI PMID:26746790 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20180201 MGI PMID:12490557 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20180201 MGI PMID:16221970 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20190822 MGI PMID:31232685 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20190822 MGI PMID:31232685 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20221006 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:19185569 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20221006 MGI PMID:35151207 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009905 absent tongue IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009905 absent tongue IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009906 increased tongue size IAGP N RGD:5509061 20221124 MGI PMID:31526805 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20180201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20220922 MGI PMID:32169905 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20221117 MGI PMID:29986157 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20221124 MGI PMID:31526805 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009913 abnormal hyoid bone greater horn morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20180201 MGI PMID:12514106 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009915 absent hyoid bone lesser horns IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009917 abnormal hyoid bone body morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20180201 MGI PMID:18501887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20180201 MGI PMID:22190459 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20180201 MGI PMID:23591430 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20180201 MGI PMID:24173031 1551747 H2az2 H2A.Z histone variant 2 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20180201 MGI PMID:21502507 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010017 visceral vascular congestion IAGP N RGD:5509061 20180201 MGI PMID:17531968 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010043 abnormal frontonasal suture morphology IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010241 abnormal aortic arch development IAGP N RGD:5509061 20180201 MGI PMID:21098571 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010252 anterior subcapsular cataract IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010361 increased gangliosarcoma incidence IAGP N RGD:5509061 20180201 MGI PMID:12469121 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010362 increased ganglioneuroma incidence IAGP N RGD:5509061 20180201 MGI PMID:12469121 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010395 abnormal pharyngeal arch development IAGP N RGD:5509061 20180201 MGI PMID:20596238 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:16332365 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:17499702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:21098571 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:36745292 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:12490557 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:16557299 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:17499702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:19008477 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010449 heart right ventricle outflow tract stenosis IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010457 pulmonary artery stenosis IAGP N RGD:5509061 20180201 MGI PMID:19008477 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010460 pulmonary artery hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:17344228 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010464 abnormal aortic arch and aortic arch branch attachment IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010464 abnormal aortic arch and aortic arch branch attachment IAGP N RGD:5509061 20180201 MGI PMID:15741317 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010464 abnormal aortic arch and aortic arch branch attachment IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20180201 MGI PMID:19008477 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010472 abnormal ascending aorta and coronary artery attachment IAGP N RGD:5509061 20180201 MGI PMID:16624854 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010485 aortic arch hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:16557299 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010563 increased heart right ventricle size IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010565 absent fetal ductus arteriosus IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010583 abnormal conotruncus morphology IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010584 abnormal conotruncus septation IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010587 conotruncal ridge hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010589 common truncal valve IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010663 abnormal brachiocephalic trunk morphology IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010706 ventral rotation of lens IAGP N RGD:5509061 20180201 MGI PMID:16207763 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010707 decreased ventral retina size IAGP N RGD:5509061 20180201 MGI PMID:16207763 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010710 absent sclera IAGP N RGD:5509061 20180201 MGI PMID:16203745 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20180201 MGI PMID:16207763 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010714 iris coloboma IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0010719 ciliary body coloboma IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:16332365 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:17693261 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:18188448 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:21982646 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:17553423 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:18440989 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:24895408 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:17172441 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:17376812 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:17610273 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:18849985 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:19605684 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:20045680 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:22745308 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:22991437 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:23454479 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:23546880 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:24173031 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20181122 MGI PMID:25818501 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20220922 MGI PMID:32169905 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221006 MGI PMID:35151207 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221006 MGI PMID:35212626 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:32692983 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221117 MGI PMID:29986157 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221124 MGI PMID:31526805 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221201 MGI PMID:24433583 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:19605684 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36745292 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:16557299 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:17499702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:22156581 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:17927973 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:33772547 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:22991437 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:23410975 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20181227 MGI PMID:27001213 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:17531968 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:18501887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:18952847 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:19008477 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:21098571 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20230504 MGI PMID:26746790 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:17344228 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:19805360 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:17183527 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011210 abnormal temporomandibular joint morphology IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20200917 MGI PMID:31733190 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011262 abnormal pharyngeal arch mesenchyme morphology IAGP N RGD:5509061 20180201 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011262 abnormal pharyngeal arch mesenchyme morphology IAGP N RGD:5509061 20180201 MGI PMID:24700590 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011615 submucous cleft palate IAGP N RGD:5509061 20220922 MGI PMID:32169905 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011627 decreased skin pigmentation IAGP N RGD:5509061 20181220 MGI PMID:21610032 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:16332365 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20240118 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20180201 MGI PMID:24895408 1551747 H2az2 H2A.Z histone variant 2 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20180503 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20181220 MGI PMID:21610032 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012077 webbed neck IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20180201 MGI PMID:17499702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:22156581 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20180201 MGI PMID:20614471 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20180201 MGI PMID:22190459 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20180201 MGI PMID:16267821 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012090 midbrain hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012091 increased midbrain size IAGP N RGD:5509061 20180201 MGI PMID:21502507 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012091 increased midbrain size IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20191114 MGI PMID:25451153 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20180201 MGI PMID:16267821 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20180201 MGI PMID:20614471 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20180201 MGI PMID:22190459 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20180201 MGI PMID:20614471 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012139 increased forebrain size IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012141 absent hindbrain IAGP N RGD:5509061 20180201 MGI PMID:22190459 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20180201 MGI PMID:20614471 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012174 flat head IAGP N RGD:5509061 20221006 MGI PMID:35212626 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012176 abnormal head development IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012260 encephalomeningocele IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012490 abnormal cochlear VIII nucleus morphology IAGP N RGD:5509061 20180201 MGI PMID:23408898 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012516 absent metencephalon IAGP N RGD:5509061 20180201 MGI PMID:11262227 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012522 abnormal stomodeum morphology IAGP N RGD:5509061 20200917 MGI PMID:31733190 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012523 abnormal upper lip morphology IAGP N RGD:5509061 20180201 MGI PMID:24700590 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20230309 MGI PMID:23872235 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012747 abnormal cardiac neural crest cell morphology IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012748 increased cardiac neural crest cell number IAGP N RGD:5509061 20180201 MGI PMID:17344228 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012749 decreased cardiac neural crest cell number IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012749 decreased cardiac neural crest cell number IAGP N RGD:5509061 20180201 MGI PMID:15789410 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012749 decreased cardiac neural crest cell number IAGP N RGD:5509061 20180201 MGI PMID:17344228 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012749 decreased cardiac neural crest cell number IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012750 absent cardiac neural crest cells IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012751 impaired cardiac neural crest cell differentiation IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012751 impaired cardiac neural crest cell differentiation IAGP N RGD:5509061 20180201 MGI PMID:17344228 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20180201 MGI PMID:15226263 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20180201 MGI PMID:15789410 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20180201 MGI PMID:17499702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012754 abnormal cranial neural crest cell morphology IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012754 abnormal cranial neural crest cell morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012754 abnormal cranial neural crest cell morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012756 impaired cranial neural crest cell differentiation IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012759 increased cranial neural crest cell proliferation IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012760 decreased cranial neural crest cell proliferation IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012760 decreased cranial neural crest cell proliferation IAGP N RGD:5509061 20180201 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012760 decreased cranial neural crest cell proliferation IAGP N RGD:5509061 20180201 MGI PMID:24700590 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012760 decreased cranial neural crest cell proliferation IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012760 decreased cranial neural crest cell proliferation IAGP N RGD:5509061 20230309 MGI PMID:23872235 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012761 increased cranial neural crest cell apoptosis IAGP N RGD:5509061 20200917 MGI PMID:31733190 1551747 H2az2 H2A.Z histone variant 2 gene MP:0012761 increased cranial neural crest cell apoptosis IAGP N RGD:5509061 20230309 MGI PMID:23872235 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013002 decreased enteric neural crest cell number IAGP N RGD:5509061 20180201 MGI PMID:19805360 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013006 abnormal enteric neural crest cell migration IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013006 abnormal enteric neural crest cell migration IAGP N RGD:5509061 20180201 MGI PMID:18693272 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013199 increased head mesenchyme apoptosis IAGP N RGD:5509061 20230309 MGI PMID:23872235 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20180201 MGI PMID:15987955 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013262 abnormal mouth floor morphology IAGP N RGD:5509061 20180201 MGI PMID:19185569 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013331 abnormal lacrimal gland development IAGP N RGD:5509061 20180201 MGI PMID:22745308 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013545 cleft hard palate IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013545 cleft hard palate IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013546 cleft soft palate IAGP N RGD:5509061 20220922 MGI PMID:32169905 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013574 ectopic parathyroid gland IAGP N RGD:5509061 20180201 MGI PMID:20498049 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013701 abnormal mature B cell number IAGP N RGD:5509061 20180201 MGI PMID:26061883 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013743 ciliary body hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:20568247 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013744 abnormal conjunctival sac morphology IAGP N RGD:5509061 20180201 MGI PMID:16207763 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013818 abnormal oral cavity morphology IAGP N RGD:5509061 20221124 MGI PMID:31526805 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20180201 MGI PMID:24895408 1551747 H2az2 H2A.Z histone variant 2 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20221124 MGI PMID:31526805 1551747 H2az2 H2A.Z histone variant 2 gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0014563 duplicated tympanic ring IAGP N RGD:5509061 20241031 MGI PMID:16221728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0020301 short tongue IAGP N RGD:5509061 20221117 MGI PMID:29986157 1551747 H2az2 H2A.Z histone variant 2 gene MP:0020393 increased neuronal precursor proliferation IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:27483349 1551747 H2az2 H2A.Z histone variant 2 gene MP:0020954 decreased mechanical nociceptive threshold IAGP N RGD:5509061 20231026 MGI PMID:28572455 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021164 oral cleft IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20220721 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20221006 MGI PMID:35151207 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20221020 MGI PMID:33772547 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20221117 MGI PMID:29986157 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021210 bilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:17927973 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:29986157 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:31526805 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:32692983 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:35212626 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:24433583 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:29986157 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:32169905 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:33772547 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:35151207 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:35212626 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021216 abnormal palatal mesenchymal cell differentiation IAGP N RGD:5509061 20230302 MGI PMID:35212626 1551747 H2az2 H2A.Z histone variant 2 gene MP:0021217 abnormal palatal shelf bone ossification IAGP N RGD:5509061 20230223 MGI PMID:17927973 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030026 small Meckel's cartilage IAGP N RGD:5509061 20180201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030026 small Meckel's cartilage IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030026 small Meckel's cartilage IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030033 abnormal nasal bridge morphology IAGP N RGD:5509061 20230504 MGI PMID:26746790 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030057 absent lacrimal bone IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030065 face hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:24700590 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030065 face hypoplasia IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030066 short face IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030069 broad face IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030072 round face IAGP N RGD:5509061 20180201 MGI PMID:24895408 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030072 round face IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030080 small lower incisors IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030085 syngnathia IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030089 short lower incisors IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030090 short upper incisors IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030102 absent orbitosphenoid bone IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030111 absent temporomandibular joint IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030112 zygomatic bone hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030119 abnormal retrotympanic process morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030120 absent retrotympanic process IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20180201 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030125 small gonial bone IAGP N RGD:5509061 20180201 MGI PMID:12514106 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030162 absent hyoid bone body IAGP N RGD:5509061 20180201 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030166 increased inner canthal distance IAGP N RGD:5509061 20180201 MGI PMID:19251646 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030166 increased inner canthal distance IAGP N RGD:5509061 20180201 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030170 absent mandibular symphysis IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030170 absent mandibular symphysis IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030189 broad snout IAGP N RGD:5509061 20221110 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030190 small snout IAGP N RGD:5509061 20180201 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030198 nasal septum hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030198 nasal septum hypoplasia IAGP N RGD:5509061 20221013 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030199 deviated nasal septum IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030200 abnormal nasal septum cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030202 nasal septum cartilage hypoplasia IAGP N RGD:5509061 20200917 MGI PMID:31733190 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030209 abnormal extrinsic tongue muscle morphology IAGP N RGD:5509061 20180201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030223 mandibular hyperostosis IAGP N RGD:5509061 20180201 MGI PMID:18367558 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030224 abnormal soft palate muscle morphology IAGP N RGD:5509061 20180201 MGI PMID:24496627 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030224 abnormal soft palate muscle morphology IAGP N RGD:5509061 20221006 MGI PMID:35212626 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030245 round head IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030249 small frontonasal prominence IAGP N RGD:5509061 20200917 MGI PMID:31733190 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030249 small frontonasal prominence IAGP N RGD:5509061 20221006 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030251 broad frontonasal prominence IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030258 small mandibular condyloid process IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030258 small mandibular condyloid process IAGP N RGD:5509061 20180201 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030258 small mandibular condyloid process IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030259 mandibular condyloid process hypoplasia IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030259 mandibular condyloid process hypoplasia IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030259 mandibular condyloid process hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030261 abnormal temporal bone zygomatic process morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030261 abnormal temporal bone zygomatic process morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030262 frontal bossing IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030268 agnathia IAGP N RGD:5509061 20180201 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030269 absent mandibular ramus IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030273 mandibular retrognathia IAGP N RGD:5509061 20180201 MGI PMID:24173031 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030276 anterior cranium occultum IAGP N RGD:5509061 20180201 MGI PMID:20106874 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030280 short parietal bone IAGP N RGD:5509061 20180201 MGI PMID:17376812 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030283 small mandibular coronoid process IAGP N RGD:5509061 20180201 MGI PMID:12975342 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030283 small mandibular coronoid process IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030283 small mandibular coronoid process IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030283 small mandibular coronoid process IAGP N RGD:5509061 20221006 MGI PMID:27362800 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030285 mandibular coronoid process hypoplasia IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030285 mandibular coronoid process hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030301 abnormal maxillary frontal process morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030302 abnormal maxillary zygomatic process morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030311 abnormal mandibular fossa morphology IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20200917 MGI PMID:31733190 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030320 abnormal temporal bone tympanic part morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030326 decreased periocular mesenchyme apoptosis IAGP N RGD:5509061 20180201 MGI PMID:16207763 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030342 small maxillary prominence IAGP N RGD:5509061 20200917 MGI PMID:31733190 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030346 small mandibular prominence IAGP N RGD:5509061 20200917 MGI PMID:31733190 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20180201 MGI PMID:19047372 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030351 wide coronal suture IAGP N RGD:5509061 20230504 MGI PMID:26746790 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030367 premature metopic suture closure IAGP N RGD:5509061 20180201 MGI PMID:19047372 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030367 premature metopic suture closure IAGP N RGD:5509061 20221110 MGI PMID:26859889 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030372 enlarged Meckel's cartilage IAGP N RGD:5509061 20180201 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030374 Meckel's cartilage hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:15107405 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030374 Meckel's cartilage hypoplasia IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030374 Meckel's cartilage hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030374 Meckel's cartilage hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030377 zygomatic arch hypoplasia IAGP N RGD:5509061 20181108 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030379 abnormal frontal bone squamous part morphology IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030383 small presphenoid bone IAGP N RGD:5509061 20220915 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030386 facial bone hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030416 absent temporal bone zygomatic process IAGP N RGD:5509061 20180201 MGI PMID:15037318 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030420 short basicranium IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030431 wide metopic suture IAGP N RGD:5509061 20221215 MGI PMID:29727702 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030431 wide metopic suture IAGP N RGD:5509061 20230504 MGI PMID:26746790 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030447 abnormal presphenoid synchondrosis IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030448 premature presphenoid synchondrosis closure IAGP N RGD:5509061 20180201 MGI PMID:18652813 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030467 abnormal cranial cartilage development IAGP N RGD:5509061 20221020 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030531 abnormal facial skin morphology IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030532 abnormal periorbital skin morphology IAGP N RGD:5509061 20180201 MGI PMID:14975722 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030536 abnormal diastema morphology IAGP N RGD:5509061 20221201 MGI PMID:24433583 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:17610273 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030681 increased circulating hydroxyproline level IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030868 absent thyroid cartilage IAGP N RGD:5509061 20181101 MGI PMID:12878728 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030869 thyroid cartilage hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030874 cricoid cartilage hypoplasia IAGP N RGD:5509061 20221027 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0030908 abnormal melanocyte differentiation IAGP N RGD:5509061 20181220 MGI PMID:21610032 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031101 nasal obstruction IAGP N RGD:5509061 20210325 MGI PMID:33431521 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031212 decreased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:19509472 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031212 decreased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:20568247 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:23134367 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031442 enlarged cerebral aqueduct IAGP N RGD:5509061 20221103 MGI PMID:34887903 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:26395480 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221110 MGI PMID:30413887 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221201 MGI PMID:24433583 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031444 glossoptosis IAGP N RGD:5509061 20221027 MGI PMID:17420000 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031444 glossoptosis IAGP N RGD:5509061 20221027 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031444 glossoptosis IAGP N RGD:5509061 20221027 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031445 midline cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:25451153 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:19541608 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:19706403 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:22219353 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031450 nasal cartilage hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:33155500 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031454 decreased cranial neural crest cell apoptosis IAGP N RGD:5509061 20221110 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031458 absent palate bones IAGP N RGD:5509061 20221124 MGI PMID:32169905 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031459 maxillary zygomatic process hypoplasia IAGP N RGD:5509061 20221201 MGI PMID:34184034 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:17376812 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:24433583 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:32541010 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20221201 MGI PMID:24433583 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:23754280 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:24785830 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:31526805 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:33772547 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031517 interrupted aortic arch, type c IAGP N RGD:5509061 20240118 MGI PMID:18058916 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031554 abnormal aortic valve development IAGP N RGD:5509061 20240125 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031555 abnormal pulmonary valve development IAGP N RGD:5509061 20240125 MGI PMID:26806701 1551747 H2az2 H2A.Z histone variant 2 gene MP:0031634 decreased heart right ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:36745292 1551748 Plekhg2 pleckstrin homology domain containing, family G (with RhoGef domain) member 2 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1551748 Plekhg2 pleckstrin homology domain containing, family G (with RhoGef domain) member 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:18273058 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:16870734 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17626887 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16870734 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18273058 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17626887 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:17626887 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17626887 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:10580504 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12101399 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17626887 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17626887 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:17626887 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12101399 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:17626887 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:17626887 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:12571362 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:17626887 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0004181 abnormal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12101399 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:12571362 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12571362 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:17626887 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:12571362 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12101399 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0008407 decreased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:10580504 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0008407 decreased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:12571362 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:10580504 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:12571362 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0008413 decreased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:10580504 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0008486 decreased muscle spindle number IAGP N RGD:5509061 20141003 MGI PMID:17626887 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:18273058 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0010021 heart vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18273058 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17626887 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17626887 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17626887 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20190704 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231221 MGI PMID:10809671 1551749 Shc1 src homology 2 domain-containing transforming protein C1 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20231221 MGI PMID:10809671 1551751 Gjb6 gap junction protein, beta 6 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:17227867 1551751 Gjb6 gap junction protein, beta 6 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:17400755 1551751 Gjb6 gap junction protein, beta 6 gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20150108 MGI PMID:24685692 1551751 Gjb6 gap junction protein, beta 6 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20150108 MGI PMID:24685692 1551751 Gjb6 gap junction protein, beta 6 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20150108 MGI PMID:24685692 1551751 Gjb6 gap junction protein, beta 6 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20150108 MGI PMID:24685692 1551751 Gjb6 gap junction protein, beta 6 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12911759 1551751 Gjb6 gap junction protein, beta 6 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:17227867 1551751 Gjb6 gap junction protein, beta 6 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:20858605 1551751 Gjb6 gap junction protein, beta 6 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12911759 1551751 Gjb6 gap junction protein, beta 6 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12911759 1551751 Gjb6 gap junction protein, beta 6 gene MP:0003849 greasy coat IAGP N RGD:5509061 20150108 MGI PMID:24685692 1551751 Gjb6 gap junction protein, beta 6 gene MP:0003879 abnormal hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19047635 1551751 Gjb6 gap junction protein, beta 6 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12490528 1551751 Gjb6 gap junction protein, beta 6 gene MP:0004368 abnormal stria vascularis vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17400755 1551751 Gjb6 gap junction protein, beta 6 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12490528 1551751 Gjb6 gap junction protein, beta 6 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17227867 1551751 Gjb6 gap junction protein, beta 6 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12490528 1551751 Gjb6 gap junction protein, beta 6 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17227867 1551751 Gjb6 gap junction protein, beta 6 gene MP:0004410 absent endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:12490528 1551751 Gjb6 gap junction protein, beta 6 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:12490528 1551751 Gjb6 gap junction protein, beta 6 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:17227867 1551751 Gjb6 gap junction protein, beta 6 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:20858605 1551751 Gjb6 gap junction protein, beta 6 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12490528 1551751 Gjb6 gap junction protein, beta 6 gene MP:0004999 abnormal blood-inner ear barrier function IAGP N RGD:5509061 20141003 MGI PMID:17400755 1551751 Gjb6 gap junction protein, beta 6 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:17400755 1551751 Gjb6 gap junction protein, beta 6 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:12911759 1551751 Gjb6 gap junction protein, beta 6 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20150108 MGI PMID:24685692 1551751 Gjb6 gap junction protein, beta 6 gene MP:0006332 abnormal cochlear potential IAGP N RGD:5509061 20141003 MGI PMID:20858605 1551751 Gjb6 gap junction protein, beta 6 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:12490528 1551751 Gjb6 gap junction protein, beta 6 gene MP:0006403 abnormal cochlear endolymph ionic homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12490528 1551751 Gjb6 gap junction protein, beta 6 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12490528 1551751 Gjb6 gap junction protein, beta 6 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17227867 1551751 Gjb6 gap junction protein, beta 6 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20858605 1551751 Gjb6 gap junction protein, beta 6 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20150108 MGI PMID:24685692 1551751 Gjb6 gap junction protein, beta 6 gene MP:0011968 decreased threshold for auditory brainstem response IAGP N RGD:5509061 20150108 MGI PMID:24685692 1551751 Gjb6 gap junction protein, beta 6 gene MP:0013378 increased sebocyte number IAGP N RGD:5509061 20150108 MGI PMID:24685692 1551752 Slpi secretory leukocyte peptidase inhibitor gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:11017147 1551752 Slpi secretory leukocyte peptidase inhibitor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18322212 1551752 Slpi secretory leukocyte peptidase inhibitor gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12615907 1551752 Slpi secretory leukocyte peptidase inhibitor gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:11017147 1551752 Slpi secretory leukocyte peptidase inhibitor gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:11017147 1551752 Slpi secretory leukocyte peptidase inhibitor gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12615907 1551752 Slpi secretory leukocyte peptidase inhibitor gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:15315966 1551752 Slpi secretory leukocyte peptidase inhibitor gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:12615907 1551752 Slpi secretory leukocyte peptidase inhibitor gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12615907 1551752 Slpi secretory leukocyte peptidase inhibitor gene MP:0008837 increased transforming growth factor beta level IAGP N RGD:5509061 20141003 MGI PMID:11017147 1551752 Slpi secretory leukocyte peptidase inhibitor gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18322212 1551753 Sf1 splicing factor 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20736371 1551753 Sf1 splicing factor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20736371 1551753 Sf1 splicing factor 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20736371 1551753 Sf1 splicing factor 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:17900258 1551753 Sf1 splicing factor 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17900258 1551753 Sf1 splicing factor 1 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20736371 1551753 Sf1 splicing factor 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17900258 1551753 Sf1 splicing factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20736371 1551754 H2-Oa histocompatibility 2, O region alpha locus gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551754 H2-Oa histocompatibility 2, O region alpha locus gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551754 H2-Oa histocompatibility 2, O region alpha locus gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551754 H2-Oa histocompatibility 2, O region alpha locus gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551754 H2-Oa histocompatibility 2, O region alpha locus gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551754 H2-Oa histocompatibility 2, O region alpha locus gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551754 H2-Oa histocompatibility 2, O region alpha locus gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551754 H2-Oa histocompatibility 2, O region alpha locus gene MP:0005041 abnormal antigen presentation via MHC class II IAGP N RGD:5509061 20141003 MGI PMID:11069069 1551754 H2-Oa histocompatibility 2, O region alpha locus gene MP:0005041 abnormal antigen presentation via MHC class II IAGP N RGD:5509061 20141003 MGI PMID:9492004 1551754 H2-Oa histocompatibility 2, O region alpha locus gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11069069 1551754 H2-Oa histocompatibility 2, O region alpha locus gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9492004 1551754 H2-Oa histocompatibility 2, O region alpha locus gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551754 H2-Oa histocompatibility 2, O region alpha locus gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551754 H2-Oa histocompatibility 2, O region alpha locus gene MP:0012702 increased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551755 Lrg1 leucine-rich alpha-2-glycoprotein 1 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20180920 MGI PMID:25826092 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16876494 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16876494 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:16876494 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:16876494 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:22349513 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22349513 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22349513 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:15657444 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:16876494 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0008156 decreased diameter of tibia IAGP N RGD:5509061 20141003 MGI PMID:16876494 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15657444 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22349513 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22349513 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:16876494 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22349513 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:16876494 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:16876494 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0021182 decreased femoral compact bone area IAGP N RGD:5509061 20220922 MGI PMID:16876494 1551756 Klf10 Kruppel-like transcription factor 10 gene MP:0030483 decreased osteocyte number IAGP N RGD:5509061 20171221 MGI PMID:16876494 1551758 Pygo2 pygopus 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20200310 MGI PMID:17425782 1551758 Pygo2 pygopus 2 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20221103 MGI 1551758 Pygo2 pygopus 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20200310 MGI PMID:17428831 1551758 Pygo2 pygopus 2 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20200310 MGI PMID:19487454 1551758 Pygo2 pygopus 2 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20200310 MGI PMID:19487454 1551758 Pygo2 pygopus 2 gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20221103 MGI 1551758 Pygo2 pygopus 2 gene MP:0000897 abnormal midbrain morphology IEA N RGD:5509061 20221103 MGI 1551758 Pygo2 pygopus 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:17425782 1551758 Pygo2 pygopus 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1551758 Pygo2 pygopus 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0001288 abnormal lens induction IAGP N RGD:5509061 20200310 MGI PMID:17428831 1551758 Pygo2 pygopus 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210128 MGI 1551758 Pygo2 pygopus 2 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20221103 MGI 1551758 Pygo2 pygopus 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:17428831 1551758 Pygo2 pygopus 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0001306 small lens IAGP N RGD:5509061 20200310 MGI PMID:17428831 1551758 Pygo2 pygopus 2 gene MP:0001306 small lens IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200310 MGI PMID:17425782 1551758 Pygo2 pygopus 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0001785 edema IEA N RGD:5509061 20221103 MGI 1551758 Pygo2 pygopus 2 gene MP:0001914 hemorrhage IEA N RGD:5509061 20221103 MGI 1551758 Pygo2 pygopus 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:23637336 1551758 Pygo2 pygopus 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:23637336 1551758 Pygo2 pygopus 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20221103 MGI 1551758 Pygo2 pygopus 2 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20221103 MGI 1551758 Pygo2 pygopus 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:17425782 1551758 Pygo2 pygopus 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:23637336 1551758 Pygo2 pygopus 2 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0003078 aphakia IAGP N RGD:5509061 20200310 MGI PMID:17425782 1551758 Pygo2 pygopus 2 gene MP:0003078 aphakia IAGP N RGD:5509061 20200310 MGI PMID:17428831 1551758 Pygo2 pygopus 2 gene MP:0003078 aphakia IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:17428831 1551758 Pygo2 pygopus 2 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20200310 MGI PMID:17425782 1551758 Pygo2 pygopus 2 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20221103 MGI 1551758 Pygo2 pygopus 2 gene MP:0004135 abnormal mammary gland embryonic development IAGP N RGD:5509061 20200310 MGI PMID:19487454 1551758 Pygo2 pygopus 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200310 MGI PMID:17425782 1551758 Pygo2 pygopus 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200310 MGI PMID:17428831 1551758 Pygo2 pygopus 2 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:17425782 1551758 Pygo2 pygopus 2 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20200310 MGI PMID:17428831 1551758 Pygo2 pygopus 2 gene MP:0005238 increased brain size IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20200310 MGI PMID:19487454 1551758 Pygo2 pygopus 2 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20200310 MGI PMID:19487454 1551758 Pygo2 pygopus 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20200310 MGI PMID:23637336 1551758 Pygo2 pygopus 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20200310 MGI 1551758 Pygo2 pygopus 2 gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:19487454 1551758 Pygo2 pygopus 2 gene MP:0010249 lactation failure IAGP N RGD:5509061 20200310 MGI PMID:19487454 1551758 Pygo2 pygopus 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17425782 1551758 Pygo2 pygopus 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17425782 1551758 Pygo2 pygopus 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17428831 1551758 Pygo2 pygopus 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17458864 1551758 Pygo2 pygopus 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551758 Pygo2 pygopus 2 gene MP:0012168 abnormal optic placode morphology IAGP N RGD:5509061 20200310 MGI PMID:17428831 1551758 Pygo2 pygopus 2 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:17425782 1551758 Pygo2 pygopus 2 gene MP:0030242 small optic pit IAGP N RGD:5509061 20200310 MGI PMID:17428831 1551760 Tspyl5 testis-specific protein, Y-encoded-like 5 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20240801 MGI PMID:38185096 1551760 Tspyl5 testis-specific protein, Y-encoded-like 5 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20240801 MGI PMID:38185096 1551760 Tspyl5 testis-specific protein, Y-encoded-like 5 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20240801 MGI PMID:38185096 1551760 Tspyl5 testis-specific protein, Y-encoded-like 5 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20240801 MGI PMID:38185096 1551760 Tspyl5 testis-specific protein, Y-encoded-like 5 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240801 MGI PMID:38185096 1551760 Tspyl5 testis-specific protein, Y-encoded-like 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20240801 MGI PMID:38185096 1551760 Tspyl5 testis-specific protein, Y-encoded-like 5 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20240801 MGI PMID:38185096 1551760 Tspyl5 testis-specific protein, Y-encoded-like 5 gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20240801 MGI PMID:38185096 1551766 Rcn1 reticulocalbin 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1551766 Rcn1 reticulocalbin 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20220811 MGI 1551766 Rcn1 reticulocalbin 1 gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 1551766 Rcn1 reticulocalbin 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210826 MGI 1551766 Rcn1 reticulocalbin 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1551766 Rcn1 reticulocalbin 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20200310 MGI 1551766 Rcn1 reticulocalbin 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1551766 Rcn1 reticulocalbin 1 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1551766 Rcn1 reticulocalbin 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20200310 MGI 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:19855011 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141009 MGI PMID:23636094 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16478991 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:19855011 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16478991 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:16478991 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20019329 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20019329 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16478991 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19855011 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16478991 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20019329 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0003279 aneurysm IAGP N RGD:5509061 20141003 MGI PMID:19855011 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0003705 abnormal hypodermis morphology IAGP N RGD:5509061 20141003 MGI PMID:16478991 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:19855011 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:19855011 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0005421 loose skin IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0005489 vascular smooth muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20019329 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:20019329 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:20019329 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:19855011 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0006135 artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:16478991 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141009 MGI PMID:23636094 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0006265 increased pulse pressure IAGP N RGD:5509061 20141009 MGI PMID:23636094 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0008418 abnormal cutaneous elastic fiber morphology IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16478991 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:19855011 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16478991 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20141009 MGI PMID:23636094 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:16478991 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141009 MGI PMID:23636094 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:20019329 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20141009 MGI PMID:23636094 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0009869 abnormal descending aorta morphology IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:17311093 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:20019329 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0010202 focal dorsal hair loss IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0010470 dilated ascending aorta IAGP N RGD:5509061 20141003 MGI PMID:19855011 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0010470 dilated ascending aorta IAGP N RGD:5509061 20141009 MGI PMID:23636094 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0010641 descending aorta stenosis IAGP N RGD:5509061 20141003 MGI PMID:16478991 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0010661 ascending aorta aneurysm IAGP N RGD:5509061 20141003 MGI PMID:20019329 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0010661 ascending aorta aneurysm IAGP N RGD:5509061 20141009 MGI PMID:23636094 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0010661 ascending aorta aneurysm IAGP N RGD:5509061 20210617 MGI PMID:19855011 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0010661 ascending aorta aneurysm IAGP N RGD:5509061 20210617 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20141003 MGI PMID:16478991 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20141009 MGI PMID:23636094 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19855011 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16478991 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20019329 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IEA N RGD:5509061 20111116 MGI 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0011157 abnormal hypodermis muscle layer morphology IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0011575 dilated aorta bulb IAGP N RGD:5509061 20210617 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20150917 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0020161 increased vascular endothelial cell proliferation IAGP N RGD:5509061 20160616 MGI PMID:20019329 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0020321 increased vascular endothelial cell apoptosis IAGP N RGD:5509061 20160616 MGI PMID:20019329 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0031086 wheezing IAGP N RGD:5509061 20200709 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0031132 increased artery tortuosity IAGP N RGD:5509061 20210617 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0031134 increased carotid artery tortuosity IAGP N RGD:5509061 20210617 MGI PMID:26178373 1551771 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2 gene MP:0031510 increased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:20019329 1551777 Adal adenosine deaminase-like gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20200402 MGI 1551777 Adal adenosine deaminase-like gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1551781 Prune1 prune exopolyphosphatase gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20111116 MGI 1551781 Prune1 prune exopolyphosphatase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551781 Prune1 prune exopolyphosphatase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1551782 Cnot6 CCR4-NOT transcription complex, subunit 6 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20210513 MGI PMID:31924127 1551782 Cnot6 CCR4-NOT transcription complex, subunit 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210513 MGI PMID:31924127 1551782 Cnot6 CCR4-NOT transcription complex, subunit 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210805 MGI PMID:34026442 1551782 Cnot6 CCR4-NOT transcription complex, subunit 6 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551783 Cnbd2 cyclic nucleotide binding domain containing 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:24339785 1551783 Cnbd2 cyclic nucleotide binding domain containing 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:24339785 1551783 Cnbd2 cyclic nucleotide binding domain containing 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:24339785 1551783 Cnbd2 cyclic nucleotide binding domain containing 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:24339785 1551783 Cnbd2 cyclic nucleotide binding domain containing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:24339785 1551783 Cnbd2 cyclic nucleotide binding domain containing 2 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:24339785 1551783 Cnbd2 cyclic nucleotide binding domain containing 2 gene MP:0004850 abnormal testis weight IAGP N RGD:5509061 20141003 MGI PMID:24339785 1551783 Cnbd2 cyclic nucleotide binding domain containing 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:24339785 1551783 Cnbd2 cyclic nucleotide binding domain containing 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:24339785 1551783 Cnbd2 cyclic nucleotide binding domain containing 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:24339785 1551783 Cnbd2 cyclic nucleotide binding domain containing 2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:24339785 1551783 Cnbd2 cyclic nucleotide binding domain containing 2 gene MP:0013209 abnormal motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:24339785 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11927618 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12861009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12861009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12126735 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:10502824 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12072562 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12126735 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12861009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12742262 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201231 MGI 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10502824 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:12072562 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:12861009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:10502824 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:14997009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12126735 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12072562 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:11927618 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:12072562 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12861009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12072562 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12861009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12000791 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12000791 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20613867 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0002570 alcohol aversion IAGP N RGD:5509061 20141003 MGI PMID:15203244 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12126735 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12072562 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12861009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20141003 MGI PMID:11579129 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:12861009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:16650144 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:20613867 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:12861009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:18305161 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:18305161 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:17272395 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:10502824 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:18305161 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:11927618 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:12861009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:12861009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0005137 increased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:17272395 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12126735 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:20613867 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12126735 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12072562 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:12072562 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:16950139 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:20613867 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:20613867 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12126735 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12861009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18305161 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12861009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0008459 abnormal circulating pancreatic peptide level IAGP N RGD:5509061 20141003 MGI PMID:12072562 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0008459 abnormal circulating pancreatic peptide level IAGP N RGD:5509061 20141003 MGI PMID:12861009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10502824 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12453895 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:11927618 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12861009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20613867 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16650144 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:20613867 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0011021 abnormal circadian regulation of heart rate IAGP N RGD:5509061 20141003 MGI PMID:10502824 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17272395 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:15203244 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:16364461 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20160407 MGI PMID:20613867 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0014145 increased white adipose tissue mass IAGP N RGD:5509061 20160407 MGI PMID:20613867 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20160407 MGI PMID:20613867 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:14997009 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0014441 decreased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:10502824 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:11927618 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:11927618 1551786 Npy2r neuropeptide Y receptor Y2 gene MP:0021198 abnormal sleep duration IAGP N RGD:5509061 20220922 MGI PMID:11579129 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:22095278 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22095278 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22095278 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:19409883 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:19409883 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22095278 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22095278 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:22095278 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19409883 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22095278 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23395638 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22095278 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:23395638 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:22095278 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22095278 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:19409883 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19409883 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:23395638 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:23395638 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:23395638 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:22095278 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:23395638 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22095278 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:19409883 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:19409883 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0008285 abnormal hippocampus granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:19409883 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0008440 abnormal subplate morphology IAGP N RGD:5509061 20141003 MGI PMID:23395638 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:19409883 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19409883 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:19409883 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:22095278 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:23395638 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19409883 1551787 Zbtb18 zinc finger and BTB domain containing 18 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:22095278 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0000753 paralysis IAGP N RGD:5509061 20180712 MGI PMID:28665968 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20180712 MGI PMID:28665968 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:19879271 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0001671 abnormal vitamin absorption IAGP N RGD:5509061 20141003 MGI PMID:19879271 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:19879271 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19879271 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20180712 MGI PMID:28665968 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20180712 MGI PMID:28665968 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20180712 MGI PMID:28665968 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19879271 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:19879271 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:19879271 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20180712 MGI PMID:28665968 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:19879271 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0009860 nephrosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19879271 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0011226 abnormal thiamin level IAGP N RGD:5509061 20141003 MGI PMID:19879271 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0011226 abnormal thiamin level IAGP N RGD:5509061 20180712 MGI PMID:28665968 1551788 Slc19a3 solute carrier family 19, member 3 gene MP:0031301 chronic liver inflammation IAGP N RGD:5509061 20211028 MGI PMID:19879271 1551792 Usf1 upstream transcription factor 1 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:9520440 1551792 Usf1 upstream transcription factor 1 gene MP:0001446 abnormal whisker trimming behavior IAGP N RGD:5509061 20141003 MGI PMID:9520440 1551792 Usf1 upstream transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9685363 1551792 Usf1 upstream transcription factor 1 gene MP:0002808 abnormal barbering behavior IAGP N RGD:5509061 20141003 MGI PMID:9520440 1551792 Usf1 upstream transcription factor 1 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:9520440 1551792 Usf1 upstream transcription factor 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9520440 1551792 Usf1 upstream transcription factor 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9520440 1551792 Usf1 upstream transcription factor 1 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:23580255 1551792 Usf1 upstream transcription factor 1 gene MP:0020468 abnormal circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:23580255 1551792 Usf1 upstream transcription factor 1 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:23580255 1551794 Iqce IQ motif containing E gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1551794 Iqce IQ motif containing E gene MP:0000745 tremors IEA N RGD:5509061 20200310 MGI 1551794 Iqce IQ motif containing E gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20200310 MGI 1551794 Iqce IQ motif containing E gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1551794 Iqce IQ motif containing E gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1551794 Iqce IQ motif containing E gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1551794 Iqce IQ motif containing E gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1551794 Iqce IQ motif containing E gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1551794 Iqce IQ motif containing E gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1551794 Iqce IQ motif containing E gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0009837 abnormal sperm end piece morphology IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551800 Styxl1 serine/threonine/tyrosine interacting-like 1 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20240808 MGI PMID:38168070 1551801 Neil3 nei like 3 (E. coli) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:16428305 1551801 Neil3 nei like 3 (E. coli) gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200310 MGI PMID:22065741 1551801 Neil3 nei like 3 (E. coli) gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20200310 MGI PMID:22065741 1551801 Neil3 nei like 3 (E. coli) gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20200310 MGI PMID:22065741 1551801 Neil3 nei like 3 (E. coli) gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20200310 MGI PMID:22065741 1551801 Neil3 nei like 3 (E. coli) gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20200310 MGI PMID:22065741 1551801 Neil3 nei like 3 (E. coli) gene MP:0020449 decreased microglial cell activation IAGP N RGD:5509061 20200310 MGI PMID:22065741 1551802 Pcgf3 polycomb group ring finger 3 gene MP:0000111 cleft palate IEA N RGD:5509061 20221215 MGI 1551802 Pcgf3 polycomb group ring finger 3 gene MP:0000562 polydactyly IEA N RGD:5509061 20221215 MGI 1551802 Pcgf3 polycomb group ring finger 3 gene MP:0000564 syndactyly IEA N RGD:5509061 20221215 MGI 1551802 Pcgf3 polycomb group ring finger 3 gene MP:0000690 absent spleen IEA N RGD:5509061 20111116 MGI 1551802 Pcgf3 polycomb group ring finger 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20221215 MGI 1551802 Pcgf3 polycomb group ring finger 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1551802 Pcgf3 polycomb group ring finger 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1551802 Pcgf3 polycomb group ring finger 3 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20221215 MGI 1551802 Pcgf3 polycomb group ring finger 3 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20221215 MGI 1551802 Pcgf3 polycomb group ring finger 3 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20221215 MGI 1551802 Pcgf3 polycomb group ring finger 3 gene MP:0008797 facial cleft IEA N RGD:5509061 20221215 MGI 1551802 Pcgf3 polycomb group ring finger 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1551802 Pcgf3 polycomb group ring finger 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1551806 Zc3h14 zinc finger CCCH type containing 14 gene MP:0001147 small testis IAGP N RGD:5509061 20180118 MGI PMID:28666327 1551806 Zc3h14 zinc finger CCCH type containing 14 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1551806 Zc3h14 zinc finger CCCH type containing 14 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210520 MGI 1551806 Zc3h14 zinc finger CCCH type containing 14 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20180118 MGI PMID:28666327 1551806 Zc3h14 zinc finger CCCH type containing 14 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20180118 MGI PMID:28666327 1551806 Zc3h14 zinc finger CCCH type containing 14 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20180118 MGI PMID:28666327 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20200310 MGI 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:30582764 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0001262 decreased body weight IEA N RGD:5509061 20200310 MGI 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:30582764 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:30582764 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200310 MGI PMID:30582764 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200310 MGI 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20200310 MGI 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:30582764 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200310 MGI PMID:30582764 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200310 MGI PMID:30582764 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:30582764 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20200310 MGI 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:30582764 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:30582764 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:30582764 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0010093 decreased circulating magnesium level IEA N RGD:5509061 20200310 MGI 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:30582764 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20200310 MGI PMID:30582764 1551807 Dusp26 dual specificity phosphatase 26 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:30582764 1551808 Lmbrd1 LMBR1 domain containing 1 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20210422 MGI PMID:27061115 1551808 Lmbrd1 LMBR1 domain containing 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1551808 Lmbrd1 LMBR1 domain containing 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20210422 MGI PMID:27061115 1551808 Lmbrd1 LMBR1 domain containing 1 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20210422 MGI PMID:27061115 1551808 Lmbrd1 LMBR1 domain containing 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20210422 MGI PMID:27061115 1551808 Lmbrd1 LMBR1 domain containing 1 gene MP:0004039 abnormal cardiac muscle cell glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:24078630 1551808 Lmbrd1 LMBR1 domain containing 1 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20240523 MGI 1551808 Lmbrd1 LMBR1 domain containing 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1551808 Lmbrd1 LMBR1 domain containing 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20210422 MGI PMID:27061115 1551808 Lmbrd1 LMBR1 domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1551808 Lmbrd1 LMBR1 domain containing 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551808 Lmbrd1 LMBR1 domain containing 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1551808 Lmbrd1 LMBR1 domain containing 1 gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:24078630 1551810 Cd226 CD226 antigen gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:19029380 1551810 Cd226 CD226 antigen gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20200310 MGI PMID:19029379 1551810 Cd226 CD226 antigen gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20200310 MGI PMID:19029380 1551810 Cd226 CD226 antigen gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:24658051 1551810 Cd226 CD226 antigen gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20200310 MGI PMID:19029379 1551810 Cd226 CD226 antigen gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20200310 MGI PMID:24658051 1551810 Cd226 CD226 antigen gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:19029380 1551810 Cd226 CD226 antigen gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20200310 MGI PMID:19029379 1551810 Cd226 CD226 antigen gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20200310 MGI PMID:19029379 1551810 Cd226 CD226 antigen gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20200310 MGI PMID:19029380 1551810 Cd226 CD226 antigen gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20200310 MGI PMID:19029379 1551810 Cd226 CD226 antigen gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20200310 MGI PMID:19029380 1551810 Cd226 CD226 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:19029380 1551810 Cd226 CD226 antigen gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:19029380 1551810 Cd226 CD226 antigen gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:19029379 1551812 Sypl1 synaptophysin like 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20231207 MGI 1551812 Sypl1 synaptophysin like 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1551812 Sypl1 synaptophysin like 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20230914 MGI PMID:37607933 1551812 Sypl1 synaptophysin like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20230914 MGI PMID:37607933 1551812 Sypl1 synaptophysin like 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20230914 MGI PMID:37607933 1551812 Sypl1 synaptophysin like 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230914 MGI PMID:37607933 1551812 Sypl1 synaptophysin like 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230914 MGI PMID:37607933 1551812 Sypl1 synaptophysin like 1 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20230914 MGI PMID:37607933 1551812 Sypl1 synaptophysin like 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20230914 MGI PMID:37607933 1551812 Sypl1 synaptophysin like 1 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20230914 MGI PMID:37607933 1551812 Sypl1 synaptophysin like 1 gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20230914 MGI PMID:37607933 1551812 Sypl1 synaptophysin like 1 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20230914 MGI PMID:37607933 1551812 Sypl1 synaptophysin like 1 gene MP:0014239 abnormal intracellular organelle morphology IAGP N RGD:5509061 20230914 MGI PMID:37607933 1551812 Sypl1 synaptophysin like 1 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20230914 MGI PMID:37607933 1551816 Tox3 TOX high mobility group box family member 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1551816 Tox3 TOX high mobility group box family member 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20200310 MGI 1551820 Lrrc8e leucine rich repeat containing 8 family, member E gene MP:0002418 increased susceptibility to viral infection IAGP N RGD:5509061 20201001 MGI PMID:32277911 1551820 Lrrc8e leucine rich repeat containing 8 family, member E gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20201001 MGI PMID:32277911 1551820 Lrrc8e leucine rich repeat containing 8 family, member E gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20201001 MGI PMID:32277911 1551820 Lrrc8e leucine rich repeat containing 8 family, member E gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20201001 MGI PMID:32277911 1551820 Lrrc8e leucine rich repeat containing 8 family, member E gene MP:0009791 increased susceptibility to viral infection induced morbidity/mortality IAGP N RGD:5509061 20201001 MGI PMID:32277911 1551820 Lrrc8e leucine rich repeat containing 8 family, member E gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20201001 MGI PMID:32277911 1551820 Lrrc8e leucine rich repeat containing 8 family, member E gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20201001 MGI PMID:32277911 1551821 Nfkbil1 nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor like 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160114 MGI 1551821 Nfkbil1 nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor like 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20160114 MGI 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12808086 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:8951074 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:8951074 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8951074 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0003109 short femur IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20221215 MGI 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20141003 MGI PMID:8951074 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:8951074 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20141003 MGI PMID:8951074 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0004627 abnormal trochanter morphology IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0004675 rib fractures IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0004987 abnormal osteoblast cell number IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:8951074 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:12808086 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:12808086 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0009445 osteomalacia IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12808086 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0010924 abnormal osteoid morphology IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0010965 decreased compact bone volume IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8951074 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808086 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0013626 decreased femur yield load IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0013633 decreased femur maximal load IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0013638 decreased femur stiffness IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0013646 decreased energy dissipated prior to femur fracture IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0013941 abnormal enthesis morphology IAGP N RGD:5509061 20160310 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20151112 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0030484 abnormal osteocyte lacuna morphology IAGP N RGD:5509061 20171221 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0030487 abnormal osteocyte dendritic process morphology IAGP N RGD:5509061 20171221 MGI PMID:24419319 1551822 Bmp1 bone morphogenetic protein 1 gene MP:0030827 femur fracture IAGP N RGD:5509061 20181018 MGI PMID:24419319 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20231207 MGI 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:24744148 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:24744148 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:24744148 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20200310 MGI PMID:11078464 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:24744148 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200310 MGI PMID:24744148 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0002574 increased vertical activity IEA N RGD:5509061 20231207 MGI 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:21998599 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20200310 MGI PMID:24744148 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20200310 MGI PMID:24744148 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0003717 pallor IAGP N RGD:5509061 20200310 MGI PMID:24744148 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0004836 abnormal synaptic acetylcholine release IAGP N RGD:5509061 20200310 MGI PMID:24744148 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:21998599 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20200310 MGI PMID:24744148 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:24744148 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24744148 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0012359 increased partial thromboplastin time IAGP N RGD:5509061 20200310 MGI PMID:24744148 1551824 Stxbp5l syntaxin binding protein 5-like gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1551825 Sc5d sterol-C5-desaturase gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0000520 absent kidney IEA N RGD:5509061 20150903 MGI 1551825 Sc5d sterol-C5-desaturase gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0000564 syndactyly IEA N RGD:5509061 20111116 MGI 1551825 Sc5d sterol-C5-desaturase gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20111116 MGI 1551825 Sc5d sterol-C5-desaturase gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0003051 curly tail IEA N RGD:5509061 20111116 MGI 1551825 Sc5d sterol-C5-desaturase gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0004361 bowed ulna IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0004385 interparietal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0004674 thin ribs IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0009160 abnormal pancreatic acinar cell zymogen granule morphology IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0010161 decreased brain cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0010422 heart right ventricle hypoplasia IEA N RGD:5509061 20150903 MGI 1551825 Sc5d sterol-C5-desaturase gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0030252 narrow frontonasal prominence IAGP N RGD:5509061 20171026 MGI PMID:12812989 1551825 Sc5d sterol-C5-desaturase gene MP:0030256 abnormal mandibular dental arch morphology IAGP N RGD:5509061 20171026 MGI PMID:12812989 1551829 Dnai4 dynein axonemal intermediate chain 4 gene MP:0001925 male infertility IEA N RGD:5509061 20230601 MGI 1551829 Dnai4 dynein axonemal intermediate chain 4 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1551832 Cklf chemokine-like factor gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20220120 MGI PMID:34446558 1551835 Smn1 survival motor neuron 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20200310 MGI PMID:11238465 1551835 Smn1 survival motor neuron 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20200310 MGI PMID:20693262 1551835 Smn1 survival motor neuron 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200310 MGI PMID:20693262 1551835 Smn1 survival motor neuron 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20200310 MGI PMID:20696672 1551835 Smn1 survival motor neuron 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20200310 MGI PMID:20696672 1551835 Smn1 survival motor neuron 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20200310 MGI PMID:21249120 1551835 Smn1 survival motor neuron 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20200310 MGI PMID:21672919 1551835 Smn1 survival motor neuron 1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0000588 thick tail IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0000588 thick tail IAGP N RGD:5509061 20200310 MGI PMID:10655541 1551835 Smn1 survival motor neuron 1 gene MP:0000592 short tail IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0000592 short tail IAGP N RGD:5509061 20200310 MGI PMID:10655541 1551835 Smn1 survival motor neuron 1 gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:10655541 1551835 Smn1 survival motor neuron 1 gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:10749994 1551835 Smn1 survival motor neuron 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0000753 paralysis IAGP N RGD:5509061 20200310 MGI PMID:11238465 1551835 Smn1 survival motor neuron 1 gene MP:0000753 paralysis IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20200310 MGI PMID:19329542 1551835 Smn1 survival motor neuron 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:10749994 1551835 Smn1 survival motor neuron 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:10655541 1551835 Smn1 survival motor neuron 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:15076752 1551835 Smn1 survival motor neuron 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200310 MGI PMID:12091709 1551835 Smn1 survival motor neuron 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200310 MGI PMID:15703193 1551835 Smn1 survival motor neuron 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200310 MGI PMID:18178576 1551835 Smn1 survival motor neuron 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200310 MGI PMID:19497369 1551835 Smn1 survival motor neuron 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20200310 MGI PMID:10749994 1551835 Smn1 survival motor neuron 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0001007 abnormal sympathetic system morphology IAGP N RGD:5509061 20200310 MGI PMID:20693262 1551835 Smn1 survival motor neuron 1 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20200310 MGI PMID:18065780 1551835 Smn1 survival motor neuron 1 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20200310 MGI PMID:15703193 1551835 Smn1 survival motor neuron 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20200310 MGI PMID:18065780 1551835 Smn1 survival motor neuron 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20200310 MGI PMID:23390132 1551835 Smn1 survival motor neuron 1 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:15076752 1551835 Smn1 survival motor neuron 1 gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:15076752 1551835 Smn1 survival motor neuron 1 gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0001212 skin lesions IEA N RGD:5509061 20111116 MGI 1551835 Smn1 survival motor neuron 1 gene MP:0001220 epidermal necrosis IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0001220 epidermal necrosis IAGP N RGD:5509061 20200310 MGI PMID:23390132 1551835 Smn1 survival motor neuron 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:15703193 1551835 Smn1 survival motor neuron 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:23390132 1551835 Smn1 survival motor neuron 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:15076752 1551835 Smn1 survival motor neuron 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:19497369 1551835 Smn1 survival motor neuron 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:20693262 1551835 Smn1 survival motor neuron 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:19497369 1551835 Smn1 survival motor neuron 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:20693262 1551835 Smn1 survival motor neuron 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:21672919 1551835 Smn1 survival motor neuron 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:23390132 1551835 Smn1 survival motor neuron 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20200310 MGI PMID:11238465 1551835 Smn1 survival motor neuron 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:20705738 1551835 Smn1 survival motor neuron 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:21672919 1551835 Smn1 survival motor neuron 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:23390132 1551835 Smn1 survival motor neuron 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:15703193 1551835 Smn1 survival motor neuron 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:19497369 1551835 Smn1 survival motor neuron 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20200310 MGI PMID:10655541 1551835 Smn1 survival motor neuron 1 gene MP:0001443 poor grooming IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20200310 MGI PMID:10749994 1551835 Smn1 survival motor neuron 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20200310 MGI PMID:15703193 1551835 Smn1 survival motor neuron 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20200310 MGI PMID:23390132 1551835 Smn1 survival motor neuron 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20200310 MGI PMID:15703193 1551835 Smn1 survival motor neuron 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20200310 MGI PMID:15703193 1551835 Smn1 survival motor neuron 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20200310 MGI PMID:9275227 1551835 Smn1 survival motor neuron 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:21249120 1551835 Smn1 survival motor neuron 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:10655541 1551835 Smn1 survival motor neuron 1 gene MP:0001956 hypopnea IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0001957 apnea IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200310 MGI PMID:10749994 1551835 Smn1 survival motor neuron 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200310 MGI PMID:15076752 1551835 Smn1 survival motor neuron 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:23390132 1551835 Smn1 survival motor neuron 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:10749994 1551835 Smn1 survival motor neuron 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:11238465 1551835 Smn1 survival motor neuron 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:15076752 1551835 Smn1 survival motor neuron 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:18178576 1551835 Smn1 survival motor neuron 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19497369 1551835 Smn1 survival motor neuron 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21672919 1551835 Smn1 survival motor neuron 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:23390132 1551835 Smn1 survival motor neuron 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:9275227 1551835 Smn1 survival motor neuron 1 gene MP:0002088 abnormal embryonic growth/weight/body size IEA N RGD:5509061 20111116 MGI 1551835 Smn1 survival motor neuron 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20111116 MGI 1551835 Smn1 survival motor neuron 1 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20200310 MGI PMID:21672919 1551835 Smn1 survival motor neuron 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20200310 MGI PMID:11238465 1551835 Smn1 survival motor neuron 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:10749994 1551835 Smn1 survival motor neuron 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0002188 small heart IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20200310 MGI PMID:20696672 1551835 Smn1 survival motor neuron 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20200310 MGI PMID:9275227 1551835 Smn1 survival motor neuron 1 gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20200310 MGI PMID:20705738 1551835 Smn1 survival motor neuron 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:20693262 1551835 Smn1 survival motor neuron 1 gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0002883 chromatolysis IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20200310 MGI PMID:19329542 1551835 Smn1 survival motor neuron 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:10749994 1551835 Smn1 survival motor neuron 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:11238465 1551835 Smn1 survival motor neuron 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0003201 extremity edema IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0003466 decreased single cell response threshold IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:20696672 1551835 Smn1 survival motor neuron 1 gene MP:0003815 hairless IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20200310 MGI PMID:11238465 1551835 Smn1 survival motor neuron 1 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20200310 MGI PMID:20693262 1551835 Smn1 survival motor neuron 1 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0003928 increased heart rate variability IAGP N RGD:5509061 20200310 MGI PMID:20693262 1551835 Smn1 survival motor neuron 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:9275227 1551835 Smn1 survival motor neuron 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0004144 hypotonia IAGP N RGD:5509061 20200310 MGI PMID:10749994 1551835 Smn1 survival motor neuron 1 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20200310 MGI PMID:19497369 1551835 Smn1 survival motor neuron 1 gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0004243 abnormal motor nerve collateral sprouting IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20200310 MGI PMID:10749994 1551835 Smn1 survival motor neuron 1 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20200310 MGI PMID:11238465 1551835 Smn1 survival motor neuron 1 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0004793 abnormal synaptic vesicle clustering IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20200310 MGI PMID:10655541 1551835 Smn1 survival motor neuron 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20200310 MGI PMID:20693262 1551835 Smn1 survival motor neuron 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20200310 MGI PMID:20696672 1551835 Smn1 survival motor neuron 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0005356 positive geotaxis IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20200310 MGI PMID:15076752 1551835 Smn1 survival motor neuron 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0005407 hyperalgesia IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0005576 decreased pulmonary ventilation IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20200310 MGI PMID:20696672 1551835 Smn1 survival motor neuron 1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20200310 MGI PMID:23390132 1551835 Smn1 survival motor neuron 1 gene MP:0006404 abnormal lumbar dorsal root ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:18178576 1551835 Smn1 survival motor neuron 1 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20200310 MGI PMID:20705738 1551835 Smn1 survival motor neuron 1 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20200310 MGI PMID:18178576 1551835 Smn1 survival motor neuron 1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20200310 MGI PMID:23390132 1551835 Smn1 survival motor neuron 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20200310 MGI PMID:18065780 1551835 Smn1 survival motor neuron 1 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20200310 MGI PMID:11238465 1551835 Smn1 survival motor neuron 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20200310 MGI PMID:11238465 1551835 Smn1 survival motor neuron 1 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20200310 MGI PMID:15703193 1551835 Smn1 survival motor neuron 1 gene MP:0009434 paraparesis IAGP N RGD:5509061 20200310 MGI PMID:19497369 1551835 Smn1 survival motor neuron 1 gene MP:0009703 decreased birth body size IEA N RGD:5509061 20111116 MGI 1551835 Smn1 survival motor neuron 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:20705738 1551835 Smn1 survival motor neuron 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:23390132 1551835 Smn1 survival motor neuron 1 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20200310 MGI PMID:11238465 1551835 Smn1 survival motor neuron 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20200310 MGI PMID:20693262 1551835 Smn1 survival motor neuron 1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20200310 MGI PMID:20696672 1551835 Smn1 survival motor neuron 1 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20200310 MGI PMID:20696672 1551835 Smn1 survival motor neuron 1 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20200310 MGI PMID:20696672 1551835 Smn1 survival motor neuron 1 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20200310 MGI PMID:23390132 1551835 Smn1 survival motor neuron 1 gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20200310 MGI PMID:23263861 1551835 Smn1 survival motor neuron 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10655541 1551835 Smn1 survival motor neuron 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15703193 1551835 Smn1 survival motor neuron 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18178576 1551835 Smn1 survival motor neuron 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19329542 1551835 Smn1 survival motor neuron 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20693262 1551835 Smn1 survival motor neuron 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20826664 1551835 Smn1 survival motor neuron 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21672919 1551835 Smn1 survival motor neuron 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22423102 1551835 Smn1 survival motor neuron 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20085811 1551835 Smn1 survival motor neuron 1 gene MP:0011088 neonatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1551835 Smn1 survival motor neuron 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10655541 1551835 Smn1 survival motor neuron 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19329542 1551835 Smn1 survival motor neuron 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10749994 1551835 Smn1 survival motor neuron 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12515823 1551835 Smn1 survival motor neuron 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551835 Smn1 survival motor neuron 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9275227 1551835 Smn1 survival motor neuron 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21249120 1551835 Smn1 survival motor neuron 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21249120 1551835 Smn1 survival motor neuron 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20696672 1551835 Smn1 survival motor neuron 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21249120 1551835 Smn1 survival motor neuron 1 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29371219 1551835 Smn1 survival motor neuron 1 gene MP:0013178 tail necrosis IAGP N RGD:5509061 20200310 MGI PMID:10615130 1551835 Smn1 survival motor neuron 1 gene MP:0013178 tail necrosis IAGP N RGD:5509061 20200310 MGI PMID:18178576 1551835 Smn1 survival motor neuron 1 gene MP:0013178 tail necrosis IAGP N RGD:5509061 20200310 MGI PMID:22802075 1551837 Zfp689 zinc finger protein 689 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1551837 Zfp689 zinc finger protein 689 gene MP:0001523 impaired righting response IEA N RGD:5509061 20181227 MGI 1551837 Zfp689 zinc finger protein 689 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20211021 MGI 1551837 Zfp689 zinc finger protein 689 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20211021 MGI 1551837 Zfp689 zinc finger protein 689 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551837 Zfp689 zinc finger protein 689 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20170105 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0000692 small spleen IEA N RGD:5509061 20210826 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210128 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0001212 skin lesions IAGP N RGD:5509061 20200310 MGI PMID:22284184 1551840 Prdm8 PR domain containing 8 gene MP:0001262 decreased body weight IEA N RGD:5509061 20210128 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20220519 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210826 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0001412 excessive scratching IAGP N RGD:5509061 20200310 MGI PMID:22284184 1551840 Prdm8 PR domain containing 8 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20200310 MGI PMID:22284184 1551840 Prdm8 PR domain containing 8 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20210520 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0002188 small heart IEA N RGD:5509061 20210826 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20200310 MGI PMID:22284184 1551840 Prdm8 PR domain containing 8 gene MP:0002311 abnormal inspiratory capacity IEA N RGD:5509061 20210128 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0002626 increased heart rate IEA N RGD:5509061 20210826 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20200310 MGI PMID:22284184 1551840 Prdm8 PR domain containing 8 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20210826 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210128 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20200310 MGI PMID:22284184 1551840 Prdm8 PR domain containing 8 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20221215 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0010935 increased airway resistance IEA N RGD:5509061 20210128 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0011044 increased lung elastance IEA N RGD:5509061 20210520 MGI 1551840 Prdm8 PR domain containing 8 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1551842 Dlst dihydrolipoamide S-succinyltransferase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19596066 1551842 Dlst dihydrolipoamide S-succinyltransferase gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19596066 1551842 Dlst dihydrolipoamide S-succinyltransferase gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:19596066 1551842 Dlst dihydrolipoamide S-succinyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1551843 Sf3b3 splicing factor 3b, subunit 3 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201022 MGI 1551843 Sf3b3 splicing factor 3b, subunit 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1551843 Sf3b3 splicing factor 3b, subunit 3 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1551843 Sf3b3 splicing factor 3b, subunit 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1551843 Sf3b3 splicing factor 3b, subunit 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201022 MGI 1551843 Sf3b3 splicing factor 3b, subunit 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551843 Sf3b3 splicing factor 3b, subunit 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551843 Sf3b3 splicing factor 3b, subunit 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1551847 Uqcrc1 ubiquinol-cytochrome c reductase core protein 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210826 MGI 1551847 Uqcrc1 ubiquinol-cytochrome c reductase core protein 1 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20200423 MGI PMID:30666338 1551847 Uqcrc1 ubiquinol-cytochrome c reductase core protein 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20200423 MGI PMID:30666338 1551847 Uqcrc1 ubiquinol-cytochrome c reductase core protein 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20200423 MGI PMID:30666338 1551847 Uqcrc1 ubiquinol-cytochrome c reductase core protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200423 MGI PMID:30666338 1551847 Uqcrc1 ubiquinol-cytochrome c reductase core protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1551847 Uqcrc1 ubiquinol-cytochrome c reductase core protein 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200423 MGI PMID:30666338 1551847 Uqcrc1 ubiquinol-cytochrome c reductase core protein 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1551850 Tmem30a transmembrane protein 30A gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180315 MGI PMID:28919113 1551850 Tmem30a transmembrane protein 30A gene MP:0000611 jaundice IAGP N RGD:5509061 20180315 MGI PMID:28919113 1551850 Tmem30a transmembrane protein 30A gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20200109 MGI PMID:28839191 1551850 Tmem30a transmembrane protein 30A gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200109 MGI PMID:28839191 1551850 Tmem30a transmembrane protein 30A gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180315 MGI PMID:28919113 1551850 Tmem30a transmembrane protein 30A gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180315 MGI PMID:28919113 1551850 Tmem30a transmembrane protein 30A gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20180315 MGI PMID:28919113 1551850 Tmem30a transmembrane protein 30A gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180315 MGI PMID:28919113 1551850 Tmem30a transmembrane protein 30A gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20180315 MGI PMID:28919113 1551850 Tmem30a transmembrane protein 30A gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200109 MGI PMID:28839191 1551850 Tmem30a transmembrane protein 30A gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20180315 MGI PMID:28919113 1551850 Tmem30a transmembrane protein 30A gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20180315 MGI PMID:28919113 1551850 Tmem30a transmembrane protein 30A gene MP:0005150 cachexia IAGP N RGD:5509061 20180315 MGI PMID:28919113 1551850 Tmem30a transmembrane protein 30A gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20180315 MGI PMID:28919113 1551850 Tmem30a transmembrane protein 30A gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20180315 MGI PMID:28919113 1551850 Tmem30a transmembrane protein 30A gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20180315 MGI PMID:28919113 1551850 Tmem30a transmembrane protein 30A gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20200109 MGI PMID:28839191 1551850 Tmem30a transmembrane protein 30A gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20200109 MGI PMID:28839191 1551850 Tmem30a transmembrane protein 30A gene MP:0008447 absent retina cone cells IAGP N RGD:5509061 20200109 MGI PMID:28839191 1551850 Tmem30a transmembrane protein 30A gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200109 MGI PMID:28839191 1551850 Tmem30a transmembrane protein 30A gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20200109 MGI PMID:28839191 1551850 Tmem30a transmembrane protein 30A gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20200109 MGI PMID:28839191 1551850 Tmem30a transmembrane protein 30A gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200109 MGI PMID:28839191 1551850 Tmem30a transmembrane protein 30A gene MP:0009773 absent retina IAGP N RGD:5509061 20200109 MGI PMID:28839191 1551850 Tmem30a transmembrane protein 30A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200109 MGI PMID:28839191 1551850 Tmem30a transmembrane protein 30A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551850 Tmem30a transmembrane protein 30A gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20180315 MGI PMID:28919113 1551850 Tmem30a transmembrane protein 30A gene MP:0020211 slow movement IAGP N RGD:5509061 20180315 MGI PMID:28919113 1551852 Crb2 crumbs family member 2 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20200310 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200310 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20200310 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0001699 increased embryo size IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20200310 MGI PMID:29539633 1551852 Crb2 crumbs family member 2 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20200310 MGI PMID:29539633 1551852 Crb2 crumbs family member 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20200310 MGI 1551852 Crb2 crumbs family member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20200310 MGI PMID:29539633 1551852 Crb2 crumbs family member 2 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20200310 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20200310 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0004559 small allantois IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20200310 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0008105 increased amacrine cell number IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0008452 increased retina rod cell number IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200310 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0010236 abnormal retina outer limiting membrane morphology IAGP N RGD:5509061 20200310 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0010236 abnormal retina outer limiting membrane morphology IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0010236 abnormal retina outer limiting membrane morphology IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29539633 1551852 Crb2 crumbs family member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551852 Crb2 crumbs family member 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0011257 abnormal head fold morphology IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0011964 increased total retina thickness IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0012081 absent heart tube IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0012104 small amniotic cavity IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20200310 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0012739 abnormal anterior primitive streak morphology IAGP N RGD:5509061 20200310 MGI PMID:22072575 1551852 Crb2 crumbs family member 2 gene MP:0014333 short retina cone cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:24493795 1551852 Crb2 crumbs family member 2 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0030006 decreased retina apoptosis IAGP N RGD:5509061 20200310 MGI PMID:24339791 1551852 Crb2 crumbs family member 2 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:23001562 1551852 Crb2 crumbs family member 2 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:24493795 1551853 Atf6b activating transcription factor 6 beta gene MP:0001192 scaly skin IEA N RGD:5509061 20181227 MGI 1551853 Atf6b activating transcription factor 6 beta gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1551853 Atf6b activating transcription factor 6 beta gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:17765680 1551853 Atf6b activating transcription factor 6 beta gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17765680 1551853 Atf6b activating transcription factor 6 beta gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551854 Rps9 ribosomal protein S9 gene MP:0000160 kyphosis IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0000414 alopecia IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0000746 weakness IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0001304 cataract IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0001577 anemia IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0002083 premature death IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0003587 ureter obstruction IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0003786 premature aging IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0010951 abnormal lipid oxidation IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551854 Rps9 ribosomal protein S9 gene MP:0031392 hypoactivity IAGP N RGD:5509061 20221201 MGI PMID:35235349 1551855 Insrr insulin receptor-related receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:11463843 1551855 Insrr insulin receptor-related receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11463843 1551855 Insrr insulin receptor-related receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11463843 1551855 Insrr insulin receptor-related receptor gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:14628051 1551855 Insrr insulin receptor-related receptor gene MP:0002893 ketoaciduria IAGP N RGD:5509061 20141003 MGI PMID:11463843 1551855 Insrr insulin receptor-related receptor gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:14628051 1551855 Insrr insulin receptor-related receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11463843 1551855 Insrr insulin receptor-related receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11463843 1551856 Unc5c unc-5 netrin receptor C gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9550145 1551856 Unc5c unc-5 netrin receptor C gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:9126743 1551856 Unc5c unc-5 netrin receptor C gene MP:0000777 increased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:9550145 1551856 Unc5c unc-5 netrin receptor C gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:9550145 1551856 Unc5c unc-5 netrin receptor C gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:14562603 1551856 Unc5c unc-5 netrin receptor C gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9126743 1551856 Unc5c unc-5 netrin receptor C gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9389662 1551856 Unc5c unc-5 netrin receptor C gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9550145 1551856 Unc5c unc-5 netrin receptor C gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:14562603 1551856 Unc5c unc-5 netrin receptor C gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:9126743 1551856 Unc5c unc-5 netrin receptor C gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:9389662 1551856 Unc5c unc-5 netrin receptor C gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9126743 1551856 Unc5c unc-5 netrin receptor C gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:9126743 1551856 Unc5c unc-5 netrin receptor C gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:9550145 1551856 Unc5c unc-5 netrin receptor C gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9389662 1551856 Unc5c unc-5 netrin receptor C gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:1401878 1551856 Unc5c unc-5 netrin receptor C gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:9126743 1551856 Unc5c unc-5 netrin receptor C gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:9389662 1551856 Unc5c unc-5 netrin receptor C gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:9550145 1551856 Unc5c unc-5 netrin receptor C gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:1401878 1551856 Unc5c unc-5 netrin receptor C gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9550145 1551856 Unc5c unc-5 netrin receptor C gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:1401878 1551856 Unc5c unc-5 netrin receptor C gene MP:0000899 abnormal corpora quadrigemina morphology IAGP N RGD:5509061 20141003 MGI PMID:14562603 1551856 Unc5c unc-5 netrin receptor C gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:16723533 1551856 Unc5c unc-5 netrin receptor C gene MP:0001063 abnormal trochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16723533 1551856 Unc5c unc-5 netrin receptor C gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16723533 1551856 Unc5c unc-5 netrin receptor C gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14562603 1551856 Unc5c unc-5 netrin receptor C gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14562603 1551856 Unc5c unc-5 netrin receptor C gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:1401878 1551856 Unc5c unc-5 netrin receptor C gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:14562603 1551856 Unc5c unc-5 netrin receptor C gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9126743 1551856 Unc5c unc-5 netrin receptor C gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9550145 1551856 Unc5c unc-5 netrin receptor C gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:14562603 1551856 Unc5c unc-5 netrin receptor C gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1551856 Unc5c unc-5 netrin receptor C gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:1401878 1551856 Unc5c unc-5 netrin receptor C gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:14562603 1551856 Unc5c unc-5 netrin receptor C gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:9550145 1551856 Unc5c unc-5 netrin receptor C gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:9550145 1551856 Unc5c unc-5 netrin receptor C gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:1401878 1551856 Unc5c unc-5 netrin receptor C gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:1401878 1551856 Unc5c unc-5 netrin receptor C gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:1401878 1551856 Unc5c unc-5 netrin receptor C gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:9126743 1551856 Unc5c unc-5 netrin receptor C gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:9389662 1551856 Unc5c unc-5 netrin receptor C gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:9550145 1551856 Unc5c unc-5 netrin receptor C gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:12451134 1551856 Unc5c unc-5 netrin receptor C gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:12451134 1551856 Unc5c unc-5 netrin receptor C gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:14562603 1551856 Unc5c unc-5 netrin receptor C gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:9389662 1551856 Unc5c unc-5 netrin receptor C gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:9126743 1551856 Unc5c unc-5 netrin receptor C gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:14562603 1551856 Unc5c unc-5 netrin receptor C gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:12451134 1551856 Unc5c unc-5 netrin receptor C gene MP:0009681 abnormal pyramidal decussation morphology IAGP N RGD:5509061 20141003 MGI PMID:12451134 1551856 Unc5c unc-5 netrin receptor C gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:9126743 1551856 Unc5c unc-5 netrin receptor C gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9550145 1551856 Unc5c unc-5 netrin receptor C gene MP:0009957 abnormal cerebellum vermis lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:9550145 1551856 Unc5c unc-5 netrin receptor C gene MP:0009960 abnormal cerebellum anterior lobe morphology IEA N RGD:5509061 20111116 MGI 1551856 Unc5c unc-5 netrin receptor C gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16723533 1551856 Unc5c unc-5 netrin receptor C gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1401878 1551856 Unc5c unc-5 netrin receptor C gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:14562603 1551856 Unc5c unc-5 netrin receptor C gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:14562603 1551856 Unc5c unc-5 netrin receptor C gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20141003 MGI PMID:16723533 1551856 Unc5c unc-5 netrin receptor C gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:14562603 1551857 Tusc3 tumor suppressor candidate 3 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1551857 Tusc3 tumor suppressor candidate 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1551857 Tusc3 tumor suppressor candidate 3 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20190502 MGI 1551857 Tusc3 tumor suppressor candidate 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551861 Sh3gl3 SH3-domain GRB2-like 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22099461 1551861 Sh3gl3 SH3-domain GRB2-like 3 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:22099461 1551861 Sh3gl3 SH3-domain GRB2-like 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22099461 1551861 Sh3gl3 SH3-domain GRB2-like 3 gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:22099461 1551861 Sh3gl3 SH3-domain GRB2-like 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22099461 1551861 Sh3gl3 SH3-domain GRB2-like 3 gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:22099461 1551861 Sh3gl3 SH3-domain GRB2-like 3 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:22099461 1551861 Sh3gl3 SH3-domain GRB2-like 3 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:22099461 1551861 Sh3gl3 SH3-domain GRB2-like 3 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:22099461 1551861 Sh3gl3 SH3-domain GRB2-like 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:22099461 1551861 Sh3gl3 SH3-domain GRB2-like 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22099461 1551861 Sh3gl3 SH3-domain GRB2-like 3 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:22099461 1551863 Trpm4 transient receptor potential cation channel, subfamily M, member 4 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18758465 1551863 Trpm4 transient receptor potential cation channel, subfamily M, member 4 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:17293867 1551863 Trpm4 transient receptor potential cation channel, subfamily M, member 4 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17293867 1551863 Trpm4 transient receptor potential cation channel, subfamily M, member 4 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:17293867 1551863 Trpm4 transient receptor potential cation channel, subfamily M, member 4 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:18758465 1551864 Fndc3b fibronectin type III domain containing 3B gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201231 MGI 1551864 Fndc3b fibronectin type III domain containing 3B gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1551864 Fndc3b fibronectin type III domain containing 3B gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210422 MGI 1551864 Fndc3b fibronectin type III domain containing 3B gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1551864 Fndc3b fibronectin type III domain containing 3B gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 1551864 Fndc3b fibronectin type III domain containing 3B gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20200310 MGI PMID:19138685 1551864 Fndc3b fibronectin type III domain containing 3B gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:19138685 1551864 Fndc3b fibronectin type III domain containing 3B gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:20493170 1551864 Fndc3b fibronectin type III domain containing 3B gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20210422 MGI 1551864 Fndc3b fibronectin type III domain containing 3B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19138685 1551864 Fndc3b fibronectin type III domain containing 3B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210422 MGI 1551864 Fndc3b fibronectin type III domain containing 3B gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:19138685 1551864 Fndc3b fibronectin type III domain containing 3B gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20200310 MGI PMID:19138685 1551864 Fndc3b fibronectin type III domain containing 3B gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20200310 MGI PMID:20493170 1551867 Zfp532 zinc finger protein 532 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1551867 Zfp532 zinc finger protein 532 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1551867 Zfp532 zinc finger protein 532 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1551867 Zfp532 zinc finger protein 532 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20230601 MGI 1551867 Zfp532 zinc finger protein 532 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20230601 MGI 1551867 Zfp532 zinc finger protein 532 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1551867 Zfp532 zinc finger protein 532 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1551869 Nqo2 N-ribosyldihydronicotinamide quinone reductase 2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:12351651 1551869 Nqo2 N-ribosyldihydronicotinamide quinone reductase 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:20861374 1551869 Nqo2 N-ribosyldihydronicotinamide quinone reductase 2 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12351651 1551869 Nqo2 N-ribosyldihydronicotinamide quinone reductase 2 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:20861374 1551869 Nqo2 N-ribosyldihydronicotinamide quinone reductase 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:12351651 1551869 Nqo2 N-ribosyldihydronicotinamide quinone reductase 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:12351651 1551869 Nqo2 N-ribosyldihydronicotinamide quinone reductase 2 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:20861374 1551869 Nqo2 N-ribosyldihydronicotinamide quinone reductase 2 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15342368 1551869 Nqo2 N-ribosyldihydronicotinamide quinone reductase 2 gene MP:0014368 enhanced long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:20861374 1551873 Wwp1 WW domain containing E3 ubiquitin protein ligase 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1551873 Wwp1 WW domain containing E3 ubiquitin protein ligase 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210826 MGI 1551873 Wwp1 WW domain containing E3 ubiquitin protein ligase 1 gene MP:0002764 short tibia IEA N RGD:5509061 20200402 MGI 1551873 Wwp1 WW domain containing E3 ubiquitin protein ligase 1 gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21809421 1551873 Wwp1 WW domain containing E3 ubiquitin protein ligase 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1551875 Vamp7 vesicle-associated membrane protein 7 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22323709 1551875 Vamp7 vesicle-associated membrane protein 7 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:22323709 1551875 Vamp7 vesicle-associated membrane protein 7 gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:22323709 1551875 Vamp7 vesicle-associated membrane protein 7 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:21740490 1551875 Vamp7 vesicle-associated membrane protein 7 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:22323709 1551876 Brd2 bromodomain containing 2 gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0000141 abnormal vertebral body morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0000153 rib bifurcation IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0000154 rib fusion IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0000161 scoliosis IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:19301389 1551876 Brd2 bromodomain containing 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19301389 1551876 Brd2 bromodomain containing 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551876 Brd2 bromodomain containing 2 gene MP:0000480 increased rib number IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0000632 abnormal pineal gland morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0000706 small thymus IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551876 Brd2 bromodomain containing 2 gene MP:0000820 abnormal choroid plexus morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0000914 exencephaly IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0001014 absent superior cervical ganglion IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0001100 abnormal vagus ganglion morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0001697 abnormal embryo size IAGP N RGD:5509061 20141003 MGI PMID:19301389 1551876 Brd2 bromodomain containing 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19301389 1551876 Brd2 bromodomain containing 2 gene MP:0001914 hemorrhage IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551876 Brd2 bromodomain containing 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551876 Brd2 bromodomain containing 2 gene MP:0002239 abnormal nasal septum morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0002746 abnormal semilunar valve morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0002747 abnormal aortic valve morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0002748 abnormal pulmonary valve morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0002951 small thyroid gland IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0002989 small kidney IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:19301389 1551876 Brd2 bromodomain containing 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551876 Brd2 bromodomain containing 2 gene MP:0003078 aphakia IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0003345 decreased rib number IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0003387 aorta coarctation IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:19301389 1551876 Brd2 bromodomain containing 2 gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551876 Brd2 bromodomain containing 2 gene MP:0004057 thin myocardium compact layer IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0004110 transposition of great arteries IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0004160 retroesophageal right subclavian artery IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0004163 abnormal adenohypophysis morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0004201 fetal growth retardation IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551876 Brd2 bromodomain containing 2 gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0004463 basisphenoid bone foramen IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0004571 absent vagus nerve IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0004603 absent vertebral arch IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0005105 abnormal middle ear ossicle morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0005236 abnormal olfactory nerve morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20181227 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0006135 artery stenosis IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0008923 thoracoschisis IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0009167 increased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0009770 abnormal optic chiasm morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0010496 abnormal pectinate muscle morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0010572 persistent right dorsal aorta IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0010589 common truncal valve IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0010853 abnormal lung position or orientation IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19883376 1551876 Brd2 bromodomain containing 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19301389 1551876 Brd2 bromodomain containing 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551876 Brd2 bromodomain containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0011380 enlarged brain ventricles IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0011659 interrupted aortic arch, type b IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0012548 myelocele IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551876 Brd2 bromodomain containing 2 gene MP:0012702 increased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:22885183 1551876 Brd2 bromodomain containing 2 gene MP:0012729 abnormal common carotid artery morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:19301389 1551876 Brd2 bromodomain containing 2 gene MP:0013809 absent pectinate muscle IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013814 abnormal hepatic portal vein connection IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013847 retropleural edema IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013852 abnormal Mullerian duct topology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013873 abnormal ductus venosus morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013874 abnormal ductus venosus topology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013879 duplication of ductus venosus IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013913 absent costovertebral joint IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013929 absent eye muscles IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013936 abnormal thymus topology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013970 absent connection between subcutaneous lymph vessels and lymph sac IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013985 abnormal umbilical vein topology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0013995 abnormal external carotid artery origin IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0014021 heterochrony IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0020483 abnormal brain artery topology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0020500 persistent trigeminal artery IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0020502 abnormal physiological umbilical hernia morphology IEA N RGD:5509061 20180628 MGI 1551876 Brd2 bromodomain containing 2 gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:19883376 1551878 Lcn8 lipocalin 8 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210603 MGI PMID:33631677 1551878 Lcn8 lipocalin 8 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210603 MGI PMID:33631677 1551878 Lcn8 lipocalin 8 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210603 MGI PMID:33631677 1551878 Lcn8 lipocalin 8 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20210603 MGI PMID:33631677 1551878 Lcn8 lipocalin 8 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20210603 MGI PMID:33631677 1551878 Lcn8 lipocalin 8 gene MP:0013288 premature acrosome reaction IAGP N RGD:5509061 20210603 MGI PMID:33631677 1551878 Lcn8 lipocalin 8 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210603 MGI PMID:33631677 1551880 Foxj3 forkhead box J3 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20201022 MGI 1551880 Foxj3 forkhead box J3 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20200310 MGI 1551880 Foxj3 forkhead box J3 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20200310 MGI 1551880 Foxj3 forkhead box J3 gene MP:0000745 tremors IEA N RGD:5509061 20201231 MGI 1551880 Foxj3 forkhead box J3 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1551880 Foxj3 forkhead box J3 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200310 MGI 1551880 Foxj3 forkhead box J3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200310 MGI 1551880 Foxj3 forkhead box J3 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20200310 MGI PMID:19914232 1551880 Foxj3 forkhead box J3 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:19914232 1551880 Foxj3 forkhead box J3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1551880 Foxj3 forkhead box J3 gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20200310 MGI PMID:19914232 1551880 Foxj3 forkhead box J3 gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20200310 MGI PMID:19914232 1551880 Foxj3 forkhead box J3 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20211021 MGI 1551880 Foxj3 forkhead box J3 gene MP:0004246 abnormal extensor digitorum longus morphology IAGP N RGD:5509061 20200310 MGI PMID:19914232 1551880 Foxj3 forkhead box J3 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20200310 MGI PMID:19914232 1551880 Foxj3 forkhead box J3 gene MP:0009410 abnormal skeletal muscle satellite cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:19914232 1551880 Foxj3 forkhead box J3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1551880 Foxj3 forkhead box J3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20200310 MGI 1551880 Foxj3 forkhead box J3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551880 Foxj3 forkhead box J3 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20200310 MGI 1551880 Foxj3 forkhead box J3 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20200310 MGI PMID:19914232 1551881 Icam2 intercellular adhesion molecule 2 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:10023766 1551881 Icam2 intercellular adhesion molecule 2 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10023766 1551881 Icam2 intercellular adhesion molecule 2 gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20141003 MGI PMID:10023766 1551885 Dsc3 desmocollin 3 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:18682494 1551885 Dsc3 desmocollin 3 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:18682494 1551885 Dsc3 desmocollin 3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:18682494 1551885 Dsc3 desmocollin 3 gene MP:0001217 absent epidermis IAGP N RGD:5509061 20141003 MGI PMID:18682494 1551885 Dsc3 desmocollin 3 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18682494 1551885 Dsc3 desmocollin 3 gene MP:0001333 absent optic nerve IEA N RGD:5509061 20181227 MGI 1551885 Dsc3 desmocollin 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1551885 Dsc3 desmocollin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16418220 1551885 Dsc3 desmocollin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18682494 1551885 Dsc3 desmocollin 3 gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:18682494 1551885 Dsc3 desmocollin 3 gene MP:0004241 acantholysis IAGP N RGD:5509061 20141003 MGI PMID:18682494 1551885 Dsc3 desmocollin 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1551885 Dsc3 desmocollin 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18682494 1551885 Dsc3 desmocollin 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18682494 1551885 Dsc3 desmocollin 3 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16418220 1551885 Dsc3 desmocollin 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551885 Dsc3 desmocollin 3 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1551885 Dsc3 desmocollin 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1551885 Dsc3 desmocollin 3 gene MP:0030578 decreased keratinocyte adhesion IAGP N RGD:5509061 20180607 MGI PMID:18682494 1551886 Tspan13 tetraspanin 13 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1551886 Tspan13 tetraspanin 13 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20230601 MGI 1551886 Tspan13 tetraspanin 13 gene MP:0002833 increased heart weight IEA N RGD:5509061 20231207 MGI 1551886 Tspan13 tetraspanin 13 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1551886 Tspan13 tetraspanin 13 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1551886 Tspan13 tetraspanin 13 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1551886 Tspan13 tetraspanin 13 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1551886 Tspan13 tetraspanin 13 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1551886 Tspan13 tetraspanin 13 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230601 MGI 1551886 Tspan13 tetraspanin 13 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1551886 Tspan13 tetraspanin 13 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1551887 Klhl9 kelch-like 9 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220811 MGI 1551887 Klhl9 kelch-like 9 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1551887 Klhl9 kelch-like 9 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1551887 Klhl9 kelch-like 9 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1551887 Klhl9 kelch-like 9 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210520 MGI 1551889 Krt1 keratin 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23132931 1551889 Krt1 keratin 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0001147 small testis IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:16528356 1551889 Krt1 keratin 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:16528356 1551889 Krt1 keratin 1 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:16528356 1551889 Krt1 keratin 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22375063 1551889 Krt1 keratin 1 gene MP:0001230 epidermal desquamation IAGP N RGD:5509061 20141003 MGI PMID:16528356 1551889 Krt1 keratin 1 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22375063 1551889 Krt1 keratin 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:16528356 1551889 Krt1 keratin 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:22375063 1551889 Krt1 keratin 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23132931 1551889 Krt1 keratin 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:16528356 1551889 Krt1 keratin 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:23132931 1551889 Krt1 keratin 1 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:16528356 1551889 Krt1 keratin 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:23132931 1551889 Krt1 keratin 1 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16528356 1551889 Krt1 keratin 1 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:23132931 1551889 Krt1 keratin 1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:23132931 1551889 Krt1 keratin 1 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:23132931 1551889 Krt1 keratin 1 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:22375063 1551889 Krt1 keratin 1 gene MP:0004930 small epididymis IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:23132931 1551889 Krt1 keratin 1 gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20141003 MGI PMID:23132931 1551889 Krt1 keratin 1 gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:23132931 1551889 Krt1 keratin 1 gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20141003 MGI PMID:22375063 1551889 Krt1 keratin 1 gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20141003 MGI PMID:23132931 1551889 Krt1 keratin 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16528356 1551889 Krt1 keratin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22375063 1551889 Krt1 keratin 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23132931 1551889 Krt1 keratin 1 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23132931 1551889 Krt1 keratin 1 gene MP:0013436 increased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20240523 MGI 1551889 Krt1 keratin 1 gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20240523 MGI 1551890 Dhps deoxyhypusine synthase gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20170706 MGI PMID:26037925 1551890 Dhps deoxyhypusine synthase gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200521 MGI PMID:21850436 1551890 Dhps deoxyhypusine synthase gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20170706 MGI PMID:26037925 1551890 Dhps deoxyhypusine synthase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170706 MGI PMID:26037925 1551890 Dhps deoxyhypusine synthase gene MP:0002083 premature death IAGP N RGD:5509061 20170706 MGI PMID:26037925 1551890 Dhps deoxyhypusine synthase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160804 MGI PMID:21389784 1551890 Dhps deoxyhypusine synthase gene MP:0005150 cachexia IAGP N RGD:5509061 20170706 MGI PMID:26037925 1551890 Dhps deoxyhypusine synthase gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20211021 MGI 1551890 Dhps deoxyhypusine synthase gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20170706 MGI PMID:26037925 1551890 Dhps deoxyhypusine synthase gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20200521 MGI PMID:21850436 1551890 Dhps deoxyhypusine synthase gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20170706 MGI PMID:26037925 1551890 Dhps deoxyhypusine synthase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20170706 MGI PMID:26037925 1551890 Dhps deoxyhypusine synthase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160804 MGI PMID:21389784 1551890 Dhps deoxyhypusine synthase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200521 MGI PMID:21850436 1551890 Dhps deoxyhypusine synthase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20201217 MGI PMID:31780266 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20210819 MGI PMID:31562139 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0001177 atelectasis IAGP N RGD:5509061 20210819 MGI PMID:31562139 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20201217 MGI PMID:31780266 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20210819 MGI PMID:31562139 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20210819 MGI PMID:31562139 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20201217 MGI PMID:31780266 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20210819 MGI PMID:31562139 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20201217 MGI PMID:31780266 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0003182 decreased pulmonary endothelial cell surface IAGP N RGD:5509061 20201217 MGI PMID:31780266 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20210819 MGI PMID:31562139 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20240523 MGI 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20210819 MGI PMID:31562139 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20210819 MGI PMID:31562139 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0010816 decreased type I pneumocyte number IAGP N RGD:5509061 20201217 MGI PMID:31780266 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20201217 MGI PMID:31780266 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20210819 MGI PMID:31562139 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0011053 decreased respiratory motile cilia number IAGP N RGD:5509061 20210819 MGI PMID:31562139 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0011071 absent club cells IAGP N RGD:5509061 20210819 MGI PMID:31562139 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210819 MGI PMID:31562139 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20201217 MGI PMID:31780266 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0014200 abnormal respiratory epithelium physiology IAGP N RGD:5509061 20210819 MGI PMID:31562139 1551892 Wfdc2 WAP four-disulfide core domain 2 gene MP:0031068 decreased blood oxygen saturation level IAGP N RGD:5509061 20201217 MGI PMID:31780266 1551894 Sh3rf1 SH3 domain containing ring finger 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220721 MGI PMID:35385725 1551894 Sh3rf1 SH3 domain containing ring finger 1 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20220721 MGI PMID:35385725 1551894 Sh3rf1 SH3 domain containing ring finger 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1551894 Sh3rf1 SH3 domain containing ring finger 1 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20220721 MGI PMID:35385725 1551894 Sh3rf1 SH3 domain containing ring finger 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20220721 MGI PMID:35385725 1551894 Sh3rf1 SH3 domain containing ring finger 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20190502 MGI 1551894 Sh3rf1 SH3 domain containing ring finger 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20220721 MGI PMID:35385725 1551894 Sh3rf1 SH3 domain containing ring finger 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20220721 MGI PMID:35385725 1551894 Sh3rf1 SH3 domain containing ring finger 1 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20220721 MGI PMID:35385725 1551894 Sh3rf1 SH3 domain containing ring finger 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20220721 MGI PMID:35385725 1551894 Sh3rf1 SH3 domain containing ring finger 1 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20220721 MGI PMID:35385725 1551894 Sh3rf1 SH3 domain containing ring finger 1 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20220721 MGI PMID:35385725 1551894 Sh3rf1 SH3 domain containing ring finger 1 gene MP:0020511 decreased dendritic spine length IAGP N RGD:5509061 20220721 MGI PMID:35385725 1551894 Sh3rf1 SH3 domain containing ring finger 1 gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20220721 MGI PMID:35385725 1551894 Sh3rf1 SH3 domain containing ring finger 1 gene MP:0031392 hypoactivity IAGP N RGD:5509061 20220721 MGI PMID:35385725 1551898 Coq2 coenzyme Q2 4-hydroxybenzoate polyprenyltransferase gene MP:0002834 decreased heart weight IEA N RGD:5509061 20200310 MGI 1551898 Coq2 coenzyme Q2 4-hydroxybenzoate polyprenyltransferase gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1551898 Coq2 coenzyme Q2 4-hydroxybenzoate polyprenyltransferase gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20200310 MGI 1551898 Coq2 coenzyme Q2 4-hydroxybenzoate polyprenyltransferase gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200310 MGI 1551898 Coq2 coenzyme Q2 4-hydroxybenzoate polyprenyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551898 Coq2 coenzyme Q2 4-hydroxybenzoate polyprenyltransferase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1551900 Nanp N-acetylneuraminic acid phosphatase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1551901 Tmed3 transmembrane p24 trafficking protein 3 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0005285 decreased unsaturated fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IEA N RGD:5509061 20111116 MGI 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20191226 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0011015 decreased body surface temperature IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0011085 postnatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551902 Dgat2 diacylglycerol O-acyltransferase 2 gene MP:0013178 tail necrosis IAGP N RGD:5509061 20141003 MGI PMID:14668353 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:17000755 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:22689653 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:17000755 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20200310 MGI PMID:22689653 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:17000755 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:17000763 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20200310 MGI PMID:17000755 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:22689653 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20200310 MGI PMID:17000755 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20200310 MGI PMID:22689653 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:22689653 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0006102 decreased tegmentum size IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20200310 MGI PMID:17000763 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22689653 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17000763 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17000755 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17000755 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17000755 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:17000763 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0012102 absent trophectoderm IAGP N RGD:5509061 20200310 MGI PMID:22689653 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20200310 MGI PMID:23798389 1551904 Gnl3 guanine nucleotide binding protein nucleolar 3 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20200310 MGI PMID:17000763 1551905 Rab11fip3 RAB11 family interacting protein 3 (class II) gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1551905 Rab11fip3 RAB11 family interacting protein 3 (class II) gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20200310 MGI 1551905 Rab11fip3 RAB11 family interacting protein 3 (class II) gene MP:0002574 increased vertical activity IEA N RGD:5509061 20200310 MGI 1551905 Rab11fip3 RAB11 family interacting protein 3 (class II) gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1551905 Rab11fip3 RAB11 family interacting protein 3 (class II) gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1551905 Rab11fip3 RAB11 family interacting protein 3 (class II) gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20240523 MGI 1551905 Rab11fip3 RAB11 family interacting protein 3 (class II) gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1551908 Or1e1c olfactory receptor family 1 subfamily E member 1C gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1551908 Or1e1c olfactory receptor family 1 subfamily E member 1C gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1551908 Or1e1c olfactory receptor family 1 subfamily E member 1C gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20230601 MGI 1551908 Or1e1c olfactory receptor family 1 subfamily E member 1C gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 1551908 Or1e1c olfactory receptor family 1 subfamily E member 1C gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20230601 MGI 1551908 Or1e1c olfactory receptor family 1 subfamily E member 1C gene MP:0004832 enlarged ovary IEA N RGD:5509061 20230601 MGI 1551908 Or1e1c olfactory receptor family 1 subfamily E member 1C gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 1551908 Or1e1c olfactory receptor family 1 subfamily E member 1C gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1551908 Or1e1c olfactory receptor family 1 subfamily E member 1C gene MP:0009476 enlarged cecum IEA N RGD:5509061 20230601 MGI 1551909 Rab31 RAB31, member RAS oncogene family gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1551913 Prkd1 protein kinase D1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1551913 Prkd1 protein kinase D1 gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:18287012 1551913 Prkd1 protein kinase D1 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1551913 Prkd1 protein kinase D1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:18287012 1551913 Prkd1 protein kinase D1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18287012 1551913 Prkd1 protein kinase D1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18287012 1551913 Prkd1 protein kinase D1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1551913 Prkd1 protein kinase D1 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18287012 1551913 Prkd1 protein kinase D1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1551913 Prkd1 protein kinase D1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20819079 1551913 Prkd1 protein kinase D1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18287012 1551913 Prkd1 protein kinase D1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20819079 1551913 Prkd1 protein kinase D1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20819079 1551915 Lrrc52 leucine rich repeat containing 52 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20200310 MGI PMID:25675513 1551915 Lrrc52 leucine rich repeat containing 52 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:25675513 1551915 Lrrc52 leucine rich repeat containing 52 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20200310 MGI PMID:25675513 1551918 Tpx2 TPX2, microtubule-associated gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0004024 aneuploidy IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0004025 polyploidy IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0008371 pituitary intermediate lobe hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0009332 abnormal splenocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1551918 Tpx2 TPX2, microtubule-associated gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22266221 1551918 Tpx2 TPX2, microtubule-associated gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0000433 microcephaly IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0000774 decreased brain size IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0000852 small cerebellum IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0001265 decreased body size IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230601 MGI 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0003604 single kidney IEA N RGD:5509061 20230601 MGI 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0010947 abnormal single-strand DNA break repair IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230601 MGI 1551919 Pnkp polynucleotide kinase 3'- phosphatase gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20161013 MGI PMID:26290337 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20200310 MGI PMID:29977031 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:25127365 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20200310 MGI PMID:25127365 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20200310 MGI PMID:25127365 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20200310 MGI PMID:25127365 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20200310 MGI PMID:25127365 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:25127365 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0004019 abnormal vitamin homeostasis IAGP N RGD:5509061 20200310 MGI PMID:25127365 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20200310 MGI PMID:29977031 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:25127365 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0005544 cornea deposits IAGP N RGD:5509061 20200310 MGI PMID:29977031 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20200310 MGI PMID:29977031 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25127365 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20200310 MGI PMID:29977031 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551920 Ubiad1 UbiA prenyltransferase domain containing 1 gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20200310 MGI PMID:29977031 1551926 Ankrd45 ankyrin repeat domain 45 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1551928 Nup85 nucleoporin 85 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200903 MGI PMID:32001710 1551928 Nup85 nucleoporin 85 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20200903 MGI PMID:32001710 1551928 Nup85 nucleoporin 85 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551928 Nup85 nucleoporin 85 gene MP:0013023 decreased Ly6C high monocyte number IAGP N RGD:5509061 20200903 MGI PMID:32001710 1551928 Nup85 nucleoporin 85 gene MP:0013026 decreased Ly6C low monocyte number IAGP N RGD:5509061 20200903 MGI PMID:32001710 1551929 Nppc natriuretic peptide type C gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11259675 1551929 Nppc natriuretic peptide type C gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17439653 1551929 Nppc natriuretic peptide type C gene MP:0000592 short tail IEA N RGD:5509061 20111116 MGI 1551929 Nppc natriuretic peptide type C gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:19805384 1551929 Nppc natriuretic peptide type C gene MP:0001147 small testis IEA N RGD:5509061 20111116 MGI 1551929 Nppc natriuretic peptide type C gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:19805384 1551929 Nppc natriuretic peptide type C gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11259675 1551929 Nppc natriuretic peptide type C gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17439653 1551929 Nppc natriuretic peptide type C gene MP:0001258 decreased body length IAGP N RGD:5509061 20220519 MGI PMID:22271248 1551929 Nppc natriuretic peptide type C gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11259675 1551929 Nppc natriuretic peptide type C gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17439653 1551929 Nppc natriuretic peptide type C gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220519 MGI PMID:22271248 1551929 Nppc natriuretic peptide type C gene MP:0001265 decreased body size IAGP N RGD:5509061 20220519 MGI PMID:22271248 1551929 Nppc natriuretic peptide type C gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11259675 1551929 Nppc natriuretic peptide type C gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:11259675 1551929 Nppc natriuretic peptide type C gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:17439653 1551929 Nppc natriuretic peptide type C gene MP:0002764 short tibia IEA N RGD:5509061 20111116 MGI 1551929 Nppc natriuretic peptide type C gene MP:0002765 short fibula IEA N RGD:5509061 20111116 MGI 1551929 Nppc natriuretic peptide type C gene MP:0003055 abnormal long bone epiphyseal plate morphology IEA N RGD:5509061 20111116 MGI 1551929 Nppc natriuretic peptide type C gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11259675 1551929 Nppc natriuretic peptide type C gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20220519 MGI PMID:22271248 1551929 Nppc natriuretic peptide type C gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:11259675 1551929 Nppc natriuretic peptide type C gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20220519 MGI PMID:22271248 1551929 Nppc natriuretic peptide type C gene MP:0004686 decreased length of long bones IEA N RGD:5509061 20111116 MGI 1551929 Nppc natriuretic peptide type C gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19805384 1551929 Nppc natriuretic peptide type C gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19805384 1551929 Nppc natriuretic peptide type C gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:20947764 1551929 Nppc natriuretic peptide type C gene MP:0006394 abnormal vertebral epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11259675 1551929 Nppc natriuretic peptide type C gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:11259675 1551929 Nppc natriuretic peptide type C gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20220519 MGI PMID:22271248 1551929 Nppc natriuretic peptide type C gene MP:0006397 disorganized long bone epiphyseal plate IEA N RGD:5509061 20111116 MGI 1551929 Nppc natriuretic peptide type C gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20220519 MGI PMID:22271248 1551929 Nppc natriuretic peptide type C gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:11259675 1551929 Nppc natriuretic peptide type C gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19805384 1551929 Nppc natriuretic peptide type C gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20220519 MGI PMID:22271248 1551929 Nppc natriuretic peptide type C gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20220519 MGI PMID:22271248 1551929 Nppc natriuretic peptide type C gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17439653 1551929 Nppc natriuretic peptide type C gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11259675 1551935 Hlx H2.0-like homeobox gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20200310 MGI PMID:8557196 1551935 Hlx H2.0-like homeobox gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20200310 MGI PMID:8557196 1551935 Hlx H2.0-like homeobox gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20200310 MGI PMID:16854219 1551935 Hlx H2.0-like homeobox gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20200310 MGI PMID:8557196 1551935 Hlx H2.0-like homeobox gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:8557196 1551935 Hlx H2.0-like homeobox gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:16854219 1551935 Hlx H2.0-like homeobox gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:8557196 1551935 Hlx H2.0-like homeobox gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:8557196 1551935 Hlx H2.0-like homeobox gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20200310 MGI PMID:16854219 1551935 Hlx H2.0-like homeobox gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20200310 MGI PMID:8557196 1551935 Hlx H2.0-like homeobox gene MP:0003250 absent gallbladder IAGP N RGD:5509061 20200310 MGI PMID:8557196 1551935 Hlx H2.0-like homeobox gene MP:0003717 pallor IAGP N RGD:5509061 20200310 MGI PMID:16854219 1551935 Hlx H2.0-like homeobox gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20200310 MGI PMID:8557196 1551935 Hlx H2.0-like homeobox gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200310 MGI PMID:16854219 1551935 Hlx H2.0-like homeobox gene MP:0004247 small pancreas IAGP N RGD:5509061 20200310 MGI PMID:8557196 1551935 Hlx H2.0-like homeobox gene MP:0004882 enlarged lung IAGP N RGD:5509061 20200310 MGI PMID:8557196 1551935 Hlx H2.0-like homeobox gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20200310 MGI PMID:16854219 1551935 Hlx H2.0-like homeobox gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16854219 1551935 Hlx H2.0-like homeobox gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:8557196 1551935 Hlx H2.0-like homeobox gene MP:0012235 abnormal liver bud morphology IAGP N RGD:5509061 20200310 MGI PMID:8557196 1551947 Arl9 ADP-ribosylation factor-like 9 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1551947 Arl9 ADP-ribosylation factor-like 9 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1551948 Atp13a2 ATPase type 13A2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:25855184 1551948 Atp13a2 ATPase type 13A2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:23393156 1551948 Atp13a2 ATPase type 13A2 gene MP:0001407 short stride length IAGP N RGD:5509061 20200310 MGI PMID:23393156 1551948 Atp13a2 ATPase type 13A2 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20200310 MGI PMID:23393156 1551948 Atp13a2 ATPase type 13A2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20200310 MGI PMID:23393156 1551948 Atp13a2 ATPase type 13A2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:25855184 1551948 Atp13a2 ATPase type 13A2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20200310 MGI PMID:23393156 1551948 Atp13a2 ATPase type 13A2 gene MP:0002183 gliosis IAGP N RGD:5509061 20200310 MGI PMID:25855184 1551948 Atp13a2 ATPase type 13A2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:23393156 1551948 Atp13a2 ATPase type 13A2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:25855184 1551948 Atp13a2 ATPase type 13A2 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20200310 MGI PMID:25855184 1551948 Atp13a2 ATPase type 13A2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200310 MGI PMID:25855184 1551948 Atp13a2 ATPase type 13A2 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20200310 MGI PMID:23393156 1551948 Atp13a2 ATPase type 13A2 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20200310 MGI PMID:25855184 1551948 Atp13a2 ATPase type 13A2 gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20200310 MGI PMID:25855184 1551948 Atp13a2 ATPase type 13A2 gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20200310 MGI PMID:23393156 1551948 Atp13a2 ATPase type 13A2 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20200310 MGI PMID:23393156 1551948 Atp13a2 ATPase type 13A2 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20200310 MGI PMID:25855184 1551948 Atp13a2 ATPase type 13A2 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200310 MGI PMID:25855184 1551949 Yif1a Yip1 interacting factor homolog A (S. cerevisiae) gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1551950 Cav2 caveolin 2 gene MP:0000730 increased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:17200204 1551950 Cav2 caveolin 2 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:17200204 1551950 Cav2 caveolin 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11884617 1551950 Cav2 caveolin 2 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:11884617 1551950 Cav2 caveolin 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1551950 Cav2 caveolin 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:11884617 1551950 Cav2 caveolin 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1551950 Cav2 caveolin 2 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17200204 1551950 Cav2 caveolin 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20160915 MGI PMID:25269481 1551950 Cav2 caveolin 2 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20160915 MGI PMID:25269481 1551950 Cav2 caveolin 2 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11884617 1551950 Cav2 caveolin 2 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20230601 MGI 1551950 Cav2 caveolin 2 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:17200204 1551950 Cav2 caveolin 2 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20160915 MGI PMID:25269481 1551950 Cav2 caveolin 2 gene MP:0010537 tumor regression IAGP N RGD:5509061 20160915 MGI PMID:25269481 1551950 Cav2 caveolin 2 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20160915 MGI PMID:25269481 1551950 Cav2 caveolin 2 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:11884617 1551951 Ak3 adenylate kinase 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:23095888 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23095888 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:12783789 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210520 MGI 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0001147 small testis IEA N RGD:5509061 20210520 MGI 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:12783789 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12783789 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:12783789 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12783789 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20141003 MGI PMID:20962251 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23095888 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12783789 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12783789 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0011760 abnormal ureteric bud tip morphology IAGP N RGD:5509061 20141003 MGI PMID:12783789 1551956 Wnt11 wingless-type MMTV integration site family, member 11 gene MP:0013401 increased endometrial gland number IAGP N RGD:5509061 20141218 MGI PMID:20962251 1551957 Or10a5 olfactory receptor family 10 subfamily A member 5 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:15186781 1551957 Or10a5 olfactory receptor family 10 subfamily A member 5 gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15186781 1551958 Cep57l1 centrosomal protein 57-like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551958 Cep57l1 centrosomal protein 57-like 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1551958 Cep57l1 centrosomal protein 57-like 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551960 Mical2 microtubule associated monooxygenase, calponin and LIM domain containing 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20231207 MGI 1551960 Mical2 microtubule associated monooxygenase, calponin and LIM domain containing 2 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20231207 MGI 1551960 Mical2 microtubule associated monooxygenase, calponin and LIM domain containing 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20231207 MGI 1551960 Mical2 microtubule associated monooxygenase, calponin and LIM domain containing 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20231207 MGI 1551960 Mical2 microtubule associated monooxygenase, calponin and LIM domain containing 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1551960 Mical2 microtubule associated monooxygenase, calponin and LIM domain containing 2 gene MP:0002188 small heart IEA N RGD:5509061 20231207 MGI 1551960 Mical2 microtubule associated monooxygenase, calponin and LIM domain containing 2 gene MP:0002989 small kidney IEA N RGD:5509061 20231207 MGI 1551960 Mical2 microtubule associated monooxygenase, calponin and LIM domain containing 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20231207 MGI 1551960 Mical2 microtubule associated monooxygenase, calponin and LIM domain containing 2 gene MP:0004357 long tibia IEA N RGD:5509061 20240523 MGI 1551960 Mical2 microtubule associated monooxygenase, calponin and LIM domain containing 2 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20231207 MGI 1551960 Mical2 microtubule associated monooxygenase, calponin and LIM domain containing 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1551960 Mical2 microtubule associated monooxygenase, calponin and LIM domain containing 2 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20231207 MGI 1551961 Krt25 keratin 25 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17920809 1551961 Krt25 keratin 25 gene MP:0000399 increased curvature of guard hairs IEA N RGD:5509061 20111116 MGI 1551961 Krt25 keratin 25 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:17920809 1551961 Krt25 keratin 25 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:17920809 1551961 Krt25 keratin 25 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17920809 1551961 Krt25 keratin 25 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:17920809 1551961 Krt25 keratin 25 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1551961 Krt25 keratin 25 gene MP:0002074 abnormal hair texture IEA N RGD:5509061 20111116 MGI 1551961 Krt25 keratin 25 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:16284798 1551961 Krt25 keratin 25 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:17920809 1551961 Krt25 keratin 25 gene MP:0008899 plush coat IEA N RGD:5509061 20111116 MGI 1551961 Krt25 keratin 25 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1551961 Krt25 keratin 25 gene MP:0010179 rough coat IEA N RGD:5509061 20111116 MGI 1551961 Krt25 keratin 25 gene MP:0010685 abnormal hair follicle inner root sheath morphology IEA N RGD:5509061 20111116 MGI 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:6391574 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:22945695 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16025116 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:6801109 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:22945695 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:22945695 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:22945695 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:6801109 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:22945695 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16025116 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:6391574 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:16025116 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:6391574 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0003582 abnormal ovary development IAGP N RGD:5509061 20160414 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16025116 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:6801109 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20160414 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20141003 MGI PMID:16025116 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004361 bowed ulna IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004373 bowed humerus IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004506 abnormal pubis morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004507 abnormal ischium morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004675 rib fractures IAGP N RGD:5509061 20141003 MGI PMID:16025116 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:6801109 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0005471 decreased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0005473 decreased triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0006322 abnormal perichondrium morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0008329 decreased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0008335 decreased gonadotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0008338 decreased thyrotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0008341 decreased corticotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:6801109 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:22945695 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0010971 abnormal periosteum morphology IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22945695 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6801109 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8456819 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0013340 abnormal pituicyte morphology IAGP N RGD:5509061 20141204 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0014162 decreased circulating cortisol level IAGP N RGD:5509061 20160414 MGI PMID:15764706 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0030542 abnormal dentin development IAGP N RGD:5509061 20180215 MGI PMID:16025116 1551964 Smpd3 sphingomyelin phosphodiesterase 3, neutral gene MP:0030856 abnormal olecranon morphology IAGP N RGD:5509061 20181025 MGI PMID:8456819 1551965 Nudt19 nudix hydrolase 19 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1551965 Nudt19 nudix hydrolase 19 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1551965 Nudt19 nudix hydrolase 19 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20170105 MGI 1551965 Nudt19 nudix hydrolase 19 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20231207 MGI 1551965 Nudt19 nudix hydrolase 19 gene MP:0005574 decreased pulmonary respiratory rate IEA N RGD:5509061 20231207 MGI 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10884307 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:10884307 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0009974 decreased cerebral cortex pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0010012 ectopic cerebral cortex pyramidal cells IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17682066 1551967 St8sia4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:17682066 1551968 Max Max protein gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:10640271 1551968 Max Max protein gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:10640271 1551968 Max Max protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10640271 1551968 Max Max protein gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10640271 1551968 Max Max protein gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10640271 1551968 Max Max protein gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:10640271 1551968 Max Max protein gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10640271 1551968 Max Max protein gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:10640271 1551969 Grm4 glutamate receptor, metabotropic 4 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:8815915 1551969 Grm4 glutamate receptor, metabotropic 4 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:8815915 1551969 Grm4 glutamate receptor, metabotropic 4 gene MP:0002922 decreased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:8815915 1551969 Grm4 glutamate receptor, metabotropic 4 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20141003 MGI 1551970 Krt27 keratin 27 gene MP:0000162 lordosis IEA N RGD:5509061 20210520 MGI 1551970 Krt27 keratin 27 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1551970 Krt27 keratin 27 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1551970 Krt27 keratin 27 gene MP:0000397 abnormal guard hair morphology IEA N RGD:5509061 20150730 MGI 1551970 Krt27 keratin 27 gene MP:0000402 abnormal zigzag hair morphology IEA N RGD:5509061 20150730 MGI 1551970 Krt27 keratin 27 gene MP:0000410 waved hair IEA N RGD:5509061 20111116 MGI 1551970 Krt27 keratin 27 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1551970 Krt27 keratin 27 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1551970 Krt27 keratin 27 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1551970 Krt27 keratin 27 gene MP:0001274 curly vibrissae IEA N RGD:5509061 20150730 MGI 1551970 Krt27 keratin 27 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1551970 Krt27 keratin 27 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1551970 Krt27 keratin 27 gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20111116 MGI 1551970 Krt27 keratin 27 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20111116 MGI 1551970 Krt27 keratin 27 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1551970 Krt27 keratin 27 gene MP:0003809 abnormal hair shaft morphology IEA N RGD:5509061 20111116 MGI 1551970 Krt27 keratin 27 gene MP:0010179 rough coat IEA N RGD:5509061 20150730 MGI 1551972 Nek6 NIMA (never in mitosis gene a)-related expressed kinase 6 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141225 MGI PMID:24763737 1551972 Nek6 NIMA (never in mitosis gene a)-related expressed kinase 6 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1551972 Nek6 NIMA (never in mitosis gene a)-related expressed kinase 6 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141225 MGI PMID:24763737 1551972 Nek6 NIMA (never in mitosis gene a)-related expressed kinase 6 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141225 MGI PMID:24763737 1551972 Nek6 NIMA (never in mitosis gene a)-related expressed kinase 6 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141225 MGI PMID:24763737 1551972 Nek6 NIMA (never in mitosis gene a)-related expressed kinase 6 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141225 MGI PMID:24763737 1551972 Nek6 NIMA (never in mitosis gene a)-related expressed kinase 6 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141225 MGI PMID:24763737 1551972 Nek6 NIMA (never in mitosis gene a)-related expressed kinase 6 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:24763737 1551973 Odc1 ornithine decarboxylase, structural 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:11533243 1551973 Odc1 ornithine decarboxylase, structural 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1551973 Odc1 ornithine decarboxylase, structural 1 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20200310 MGI PMID:11533243 1551973 Odc1 ornithine decarboxylase, structural 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11533243 1551973 Odc1 ornithine decarboxylase, structural 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551973 Odc1 ornithine decarboxylase, structural 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1551974 Fzd5 frizzled class receptor 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1551974 Fzd5 frizzled class receptor 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1551974 Fzd5 frizzled class receptor 5 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20191219 MGI PMID:18791178 1551974 Fzd5 frizzled class receptor 5 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:18509025 1551974 Fzd5 frizzled class receptor 5 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1551974 Fzd5 frizzled class receptor 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18509025 1551974 Fzd5 frizzled class receptor 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18509025 1551974 Fzd5 frizzled class receptor 5 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20191219 MGI PMID:18791178 1551974 Fzd5 frizzled class receptor 5 gene MP:0001306 small lens IAGP N RGD:5509061 20191219 MGI PMID:18791178 1551974 Fzd5 frizzled class receptor 5 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:18509025 1551974 Fzd5 frizzled class receptor 5 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18509025 1551974 Fzd5 frizzled class receptor 5 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:11092808 1551974 Fzd5 frizzled class receptor 5 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:11092808 1551974 Fzd5 frizzled class receptor 5 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:11092808 1551974 Fzd5 frizzled class receptor 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11092808 1551974 Fzd5 frizzled class receptor 5 gene MP:0003099 retina detachment IAGP N RGD:5509061 20191219 MGI PMID:18791178 1551974 Fzd5 frizzled class receptor 5 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20191219 MGI PMID:18489003 1551974 Fzd5 frizzled class receptor 5 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20191219 MGI PMID:18791178 1551974 Fzd5 frizzled class receptor 5 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:11092808 1551974 Fzd5 frizzled class receptor 5 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20191219 MGI PMID:18489003 1551974 Fzd5 frizzled class receptor 5 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20191219 MGI PMID:18489003 1551974 Fzd5 frizzled class receptor 5 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20191219 MGI PMID:18791178 1551974 Fzd5 frizzled class receptor 5 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20191219 MGI PMID:18489003 1551974 Fzd5 frizzled class receptor 5 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20191219 MGI PMID:18791178 1551974 Fzd5 frizzled class receptor 5 gene MP:0006200 vitreous body deposition IAGP N RGD:5509061 20191219 MGI PMID:18791178 1551974 Fzd5 frizzled class receptor 5 gene MP:0008509 disorganized retina ganglion layer IAGP N RGD:5509061 20191219 MGI PMID:18791178 1551974 Fzd5 frizzled class receptor 5 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11092808 1551974 Fzd5 frizzled class receptor 5 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1551974 Fzd5 frizzled class receptor 5 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11092808 1551974 Fzd5 frizzled class receptor 5 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18509025 1551974 Fzd5 frizzled class receptor 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551974 Fzd5 frizzled class receptor 5 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20191219 MGI PMID:18791178 1551974 Fzd5 frizzled class receptor 5 gene MP:0011964 increased total retina thickness IAGP N RGD:5509061 20191219 MGI PMID:18791178 1551974 Fzd5 frizzled class receptor 5 gene MP:0014077 ectopic Paneth cells IAGP N RGD:5509061 20160310 MGI PMID:15778706 1551974 Fzd5 frizzled class receptor 5 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:18791178 1551974 Fzd5 frizzled class receptor 5 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20191219 MGI PMID:18489003 1551975 Ddx52 DExD box helicase 52 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1551975 Ddx52 DExD box helicase 52 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1551975 Ddx52 DExD box helicase 52 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20160804 MGI 1551979 Coq4 coenzyme Q4 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20200310 MGI PMID:29539633 1551979 Coq4 coenzyme Q4 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20200310 MGI PMID:29539633 1551979 Coq4 coenzyme Q4 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20200310 MGI PMID:29539633 1551979 Coq4 coenzyme Q4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29539633 1551979 Coq4 coenzyme Q4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551980 Pskh1 protein serine kinase H1 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1551980 Pskh1 protein serine kinase H1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20160929 MGI PMID:27534441 1551980 Pskh1 protein serine kinase H1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1551980 Pskh1 protein serine kinase H1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1551980 Pskh1 protein serine kinase H1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1551980 Pskh1 protein serine kinase H1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 1551980 Pskh1 protein serine kinase H1 gene MP:0010853 abnormal lung position or orientation IEA N RGD:5509061 20141003 MGI 1551980 Pskh1 protein serine kinase H1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551980 Pskh1 protein serine kinase H1 gene MP:0011252 situs inversus totalis IEA N RGD:5509061 20141003 MGI 1551980 Pskh1 protein serine kinase H1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1551984 Mtarc2 mitochondrial amidoxime reducing component 2 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20240509 MGI PMID:38437227 1551984 Mtarc2 mitochondrial amidoxime reducing component 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240509 MGI PMID:38437227 1551984 Mtarc2 mitochondrial amidoxime reducing component 2 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20240509 MGI PMID:38437227 1551985 Eml3 echinoderm microtubule associated protein like 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 1551987 Ints12 integrator complex subunit 12 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1551987 Ints12 integrator complex subunit 12 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1551987 Ints12 integrator complex subunit 12 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1551987 Ints12 integrator complex subunit 12 gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20160804 MGI 1551987 Ints12 integrator complex subunit 12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:17318223 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:7698643 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:17318223 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20240523 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20240523 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001214 skin hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:7698643 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:9207086 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20240523 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20200310 MGI PMID:9207086 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:17318223 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:12727891 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:15489954 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:17184942 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:15489954 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:15494543 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:9922314 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:12727891 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:12727891 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:9207086 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20240523 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:15489954 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20200310 MGI PMID:15554929 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20200310 MGI PMID:9922314 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20200310 MGI PMID:17184942 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:11097843 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:15699164 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20200310 MGI PMID:15699164 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20200310 MGI PMID:15699164 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0003701 elevated level of mitotic sister chromatid exchange IAGP N RGD:5509061 20200310 MGI PMID:9207086 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20200310 MGI PMID:17318223 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20201231 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20200310 MGI PMID:21270334 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20200310 MGI PMID:12727891 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20200310 MGI PMID:17318223 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20200310 MGI PMID:9207086 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20200310 MGI PMID:15494543 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20200310 MGI PMID:9207086 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0004925 decreased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20200310 MGI PMID:17184942 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20200310 MGI PMID:15554929 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0005387 immune system phenotype IEA N RGD:5509061 20201022 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0005527 increased renal glomerular filtration rate IAGP N RGD:5509061 20200310 MGI PMID:15494543 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20240523 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20200310 MGI PMID:15494543 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:9207086 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20210128 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20200310 MGI PMID:9207086 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20200310 MGI PMID:15489954 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20200310 MGI PMID:15489954 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20200310 MGI PMID:15489954 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20200310 MGI PMID:12727891 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:10051636 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:15699164 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:9207086 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200310 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20210128 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12727891 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17318223 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9207086 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12727891 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0011372 decreased renal tubule apoptosis IAGP N RGD:5509061 20200310 MGI PMID:15494543 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20200310 MGI PMID:7698643 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20200310 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20200310 MGI PMID:17318223 1551988 Parp1 poly (ADP-ribose) polymerase family, member 1 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20230824 MGI PMID:17318223 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0000126 brittle teeth IAGP N RGD:5509061 20180125 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0000132 thickened long bone epiphysis IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0003671 abnormal eyelid aperture IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0004540 small maxilla IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0006198 enophthalmos IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20220915 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:18985159 1551989 Slc39a13 solute carrier family 39 (metal ion transporter), member 13 gene MP:0030494 abnormal molar root morphology IAGP N RGD:5509061 20180125 MGI PMID:18985159 1551991 Cnmd chondromodulin gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12509461 1551991 Cnmd chondromodulin gene MP:0000064 failure of bone resorption IAGP N RGD:5509061 20141003 MGI PMID:12509461 1551991 Cnmd chondromodulin gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:12509461 1551991 Cnmd chondromodulin gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:12509461 1551991 Cnmd chondromodulin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12192060 1551991 Cnmd chondromodulin gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:12509461 1551991 Cnmd chondromodulin gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:12509461 1551991 Cnmd chondromodulin gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12509461 1551991 Cnmd chondromodulin gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20220922 MGI PMID:12509461 1551991 Cnmd chondromodulin gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:12509461 1551993 Dtl denticleless E3 ubiquitin protein ligase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 1551993 Dtl denticleless E3 ubiquitin protein ligase gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17107960 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20693420 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12208842 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12208842 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:12208842 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:12208842 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0001411 spinning IAGP N RGD:5509061 20141003 MGI PMID:12208842 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20200709 MGI PMID:24648452 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20693420 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:12208842 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12208842 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12208842 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20693420 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20693420 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20693420 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:12208842 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:12208842 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20693420 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20200709 MGI PMID:24648452 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20200709 MGI PMID:24648452 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:20693420 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20200709 MGI PMID:24648452 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20693420 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20693420 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20200709 MGI PMID:24648452 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:20693420 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:16382139 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20693420 1551994 Usp18 ubiquitin specific peptidase 18 gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200709 MGI PMID:24648452 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20817122 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20817122 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20141003 MGI PMID:20830789 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:20817122 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20141003 MGI PMID:20830789 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20817122 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:20817122 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20817122 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20830789 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20830789 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20830789 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0010967 increased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:20817122 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1551996 P2ry13 purinergic receptor P2Y, G-protein coupled 13 gene MP:0014480 increased feces cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:20817122 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220519 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:1759682 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:2164218 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:16904100 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0001258 decreased body length IEA N RGD:5509061 20210520 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210520 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210520 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:16904100 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:1759682 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:2164218 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:1759682 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0002764 short tibia IEA N RGD:5509061 20210520 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20200310 MGI PMID:1759682 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20200310 MGI PMID:2164218 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20210520 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0002834 decreased heart weight IEA N RGD:5509061 20210520 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210520 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210520 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:1759682 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:2164218 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20220519 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20240523 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210520 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20210520 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1551997 Fndc3a fibronectin type III domain containing 3A gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20200310 MGI PMID:2164218 1551998 Mpp2 membrane protein, palmitoylated 2 (MAGUK p55 subfamily member 2) gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210520 MGI 1551998 Mpp2 membrane protein, palmitoylated 2 (MAGUK p55 subfamily member 2) gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1551998 Mpp2 membrane protein, palmitoylated 2 (MAGUK p55 subfamily member 2) gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1551998 Mpp2 membrane protein, palmitoylated 2 (MAGUK p55 subfamily member 2) gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1552001 Wdr27 WD repeat domain 27 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20231207 MGI 1552001 Wdr27 WD repeat domain 27 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20231207 MGI 1552001 Wdr27 WD repeat domain 27 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 1552001 Wdr27 WD repeat domain 27 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20231207 MGI 1552001 Wdr27 WD repeat domain 27 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20240523 MGI 1552001 Wdr27 WD repeat domain 27 gene MP:0003394 increased cardiac output IEA N RGD:5509061 20240523 MGI 1552001 Wdr27 WD repeat domain 27 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1552001 Wdr27 WD repeat domain 27 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1552001 Wdr27 WD repeat domain 27 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20240523 MGI 1552001 Wdr27 WD repeat domain 27 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20240523 MGI 1552001 Wdr27 WD repeat domain 27 gene MP:0010574 dilated aorta IEA N RGD:5509061 20240523 MGI 1552002 Ppp2r1b protein phosphatase 2, regulatory subunit A, beta gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1552002 Ppp2r1b protein phosphatase 2, regulatory subunit A, beta gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20201231 MGI 1552002 Ppp2r1b protein phosphatase 2, regulatory subunit A, beta gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20305648 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23637822 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20200116 MGI PMID:29669747 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18971423 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:16675847 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:16675847 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:16675847 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20200116 MGI PMID:29669747 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17652758 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17909628 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23637822 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:17909628 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200116 MGI PMID:29669747 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:16675847 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20191003 MGI PMID:30675063 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17652758 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16732273 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15653504 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20191003 MGI PMID:30675063 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23334413 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16809547 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18843253 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21060874 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:23637822 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20220811 MGI 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20200116 MGI PMID:29669747 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210128 MGI 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16732273 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20200827 MGI PMID:31771656 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:20305648 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16732273 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20305648 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20200116 MGI PMID:29669747 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17909628 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:23637822 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20200116 MGI PMID:29669747 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:11544273 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12569158 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:18843253 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20210211 MGI PMID:32755573 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:18843253 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16675847 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21060874 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:16809547 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:15653504 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17652758 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:23637822 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17652758 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17652758 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:23637822 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23637822 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12569158 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12600915 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20200827 MGI PMID:31771656 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005546 choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:17652758 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005546 choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:17909628 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23637822 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20141003 MGI PMID:17652758 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20141003 MGI PMID:23637822 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005549 retina pigment epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17652758 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:11544273 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0006051 brainstem hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16675847 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20200827 MGI PMID:31771656 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0006187 retina deposits IAGP N RGD:5509061 20141003 MGI PMID:17652758 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0006187 retina deposits IAGP N RGD:5509061 20141003 MGI PMID:17909628 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:16675847 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:15653504 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23334413 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20200116 MGI PMID:29669747 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20200116 MGI PMID:29669747 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:17652758 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:23637822 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:17909628 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200116 MGI PMID:29669747 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20210211 MGI PMID:32755573 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20200827 MGI PMID:31771656 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:17652758 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:23637822 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200116 MGI PMID:29669747 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200827 MGI PMID:31771656 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20200827 MGI PMID:31771656 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20200827 MGI PMID:31771656 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20200827 MGI PMID:31771656 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008837 increased transforming growth factor beta level IAGP N RGD:5509061 20200827 MGI PMID:31771656 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:16732273 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20200827 MGI PMID:31771656 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:16732273 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:12600915 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0009392 retina gliosis IAGP N RGD:5509061 20200116 MGI PMID:29669747 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20211202 MGI PMID:32923620 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16675847 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200827 MGI PMID:31771656 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15653504 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0010016 variable depigmentation IAGP N RGD:5509061 20141003 MGI PMID:17652758 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16732273 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:16732273 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20210211 MGI PMID:32755573 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11544273 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16675847 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:16732273 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:29669747 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:29669747 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20210211 MGI PMID:32755573 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20200116 MGI PMID:29669747 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:23637822 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0031509 decreased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:16809547 1552004 Cx3cr1 C-X3-C motif chemokine receptor 1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:23637822 1552006 Dag1 dystroglycan 1 gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:12140559 1552006 Dag1 dystroglycan 1 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:12230980 1552006 Dag1 dystroglycan 1 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:21388311 1552006 Dag1 dystroglycan 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12230980 1552006 Dag1 dystroglycan 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12140559 1552006 Dag1 dystroglycan 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:12140559 1552006 Dag1 dystroglycan 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20240801 MGI PMID:38616731 1552006 Dag1 dystroglycan 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:12140559 1552006 Dag1 dystroglycan 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:18579745 1552006 Dag1 dystroglycan 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:18794334 1552006 Dag1 dystroglycan 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:21388311 1552006 Dag1 dystroglycan 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240801 MGI PMID:38616731 1552006 Dag1 dystroglycan 1 gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:12230980 1552006 Dag1 dystroglycan 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19846701 1552006 Dag1 dystroglycan 1 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:19846701 1552006 Dag1 dystroglycan 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12140559 1552006 Dag1 dystroglycan 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:21388311 1552006 Dag1 dystroglycan 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9175728 1552006 Dag1 dystroglycan 1 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:9175728 1552006 Dag1 dystroglycan 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9175728 1552006 Dag1 dystroglycan 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20240801 MGI PMID:38616731 1552006 Dag1 dystroglycan 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9175728 1552006 Dag1 dystroglycan 1 gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:19846701 1552006 Dag1 dystroglycan 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9175728 1552006 Dag1 dystroglycan 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9175728 1552006 Dag1 dystroglycan 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20240801 MGI PMID:38616731 1552006 Dag1 dystroglycan 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12140559 1552006 Dag1 dystroglycan 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22810924 1552006 Dag1 dystroglycan 1 gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:19846701 1552006 Dag1 dystroglycan 1 gene MP:0002583 absent extraembryonic ectoderm IAGP N RGD:5509061 20141003 MGI PMID:9175728 1552006 Dag1 dystroglycan 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:19797173 1552006 Dag1 dystroglycan 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:23217742 1552006 Dag1 dystroglycan 1 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19797173 1552006 Dag1 dystroglycan 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20240801 MGI PMID:38616731 1552006 Dag1 dystroglycan 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19797173 1552006 Dag1 dystroglycan 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:12140559 1552006 Dag1 dystroglycan 1 gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:12230980 1552006 Dag1 dystroglycan 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:18579745 1552006 Dag1 dystroglycan 1 gene MP:0003954 abnormal Reichert's membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:9175728 1552006 Dag1 dystroglycan 1 gene MP:0003954 abnormal Reichert's membrane morphology IAGP N RGD:5509061 20240801 MGI PMID:38616731 1552006 Dag1 dystroglycan 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19846701 1552006 Dag1 dystroglycan 1 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12140559 1552006 Dag1 dystroglycan 1 gene MP:0004262 abnormal physical strength IAGP N RGD:5509061 20240801 MGI PMID:38616731 1552006 Dag1 dystroglycan 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:23217742 1552006 Dag1 dystroglycan 1 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:19797173 1552006 Dag1 dystroglycan 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22810924 1552006 Dag1 dystroglycan 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:12140559 1552006 Dag1 dystroglycan 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:18579745 1552006 Dag1 dystroglycan 1 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:18579745 1552006 Dag1 dystroglycan 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:18579745 1552006 Dag1 dystroglycan 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12140559 1552006 Dag1 dystroglycan 1 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:12140559 1552006 Dag1 dystroglycan 1 gene MP:0008285 abnormal hippocampus granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:12140559 1552006 Dag1 dystroglycan 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:18579745 1552006 Dag1 dystroglycan 1 gene MP:0009027 abnormal subarachnoid space morphology IAGP N RGD:5509061 20141003 MGI PMID:12140559 1552006 Dag1 dystroglycan 1 gene MP:0009274 buphthalmos IAGP N RGD:5509061 20141003 MGI PMID:19846701 1552006 Dag1 dystroglycan 1 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:12230980 1552006 Dag1 dystroglycan 1 gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:12230980 1552006 Dag1 dystroglycan 1 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:12230980 1552006 Dag1 dystroglycan 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:12230980 1552006 Dag1 dystroglycan 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:21388311 1552006 Dag1 dystroglycan 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:22810924 1552006 Dag1 dystroglycan 1 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:23217742 1552006 Dag1 dystroglycan 1 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:23217742 1552006 Dag1 dystroglycan 1 gene MP:0009695 abnormal spinal cord ventral commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:23217742 1552006 Dag1 dystroglycan 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:21388311 1552006 Dag1 dystroglycan 1 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:12230980 1552006 Dag1 dystroglycan 1 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:22810924 1552006 Dag1 dystroglycan 1 gene MP:0010238 increased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:12230980 1552006 Dag1 dystroglycan 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19846701 1552006 Dag1 dystroglycan 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240801 MGI PMID:38616731 1552006 Dag1 dystroglycan 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9175728 1552006 Dag1 dystroglycan 1 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20150430 MGI PMID:19846701 1552006 Dag1 dystroglycan 1 gene MP:0020391 radial glial endfoot detachment IAGP N RGD:5509061 20161117 MGI PMID:23217742 1552006 Dag1 dystroglycan 1 gene MP:0021155 abnormal heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:19797173 1552007 Zfp184 zinc finger protein 184 (Kruppel-like) gene MP:0004924 abnormal behavior IEA N RGD:5509061 20200310 MGI 1552008 Gip gastric inhibitory polypeptide gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1552009 Bcl2l1 BCL2-like 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:17382885 1552009 Bcl2l1 BCL2-like 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:15905539 1552009 Bcl2l1 BCL2-like 1 gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20200310 MGI PMID:18566418 1552009 Bcl2l1 BCL2-like 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:11150333 1552009 Bcl2l1 BCL2-like 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20200310 MGI PMID:11150333 1552009 Bcl2l1 BCL2-like 1 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20200310 MGI PMID:10894153 1552009 Bcl2l1 BCL2-like 1 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:10894153 1552009 Bcl2l1 BCL2-like 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:10894153 1552009 Bcl2l1 BCL2-like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:16033881 1552009 Bcl2l1 BCL2-like 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20200310 MGI PMID:10894153 1552009 Bcl2l1 BCL2-like 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:10894153 1552009 Bcl2l1 BCL2-like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:10894153 1552009 Bcl2l1 BCL2-like 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:10894153 1552009 Bcl2l1 BCL2-like 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200310 MGI PMID:16033881 1552009 Bcl2l1 BCL2-like 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20200310 MGI PMID:16033881 1552009 Bcl2l1 BCL2-like 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:12093873 1552009 Bcl2l1 BCL2-like 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200310 MGI PMID:17382885 1552009 Bcl2l1 BCL2-like 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:11150333 1552009 Bcl2l1 BCL2-like 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:9096145 1552009 Bcl2l1 BCL2-like 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:9096145 1552009 Bcl2l1 BCL2-like 1 gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20200310 MGI PMID:16033881 1552009 Bcl2l1 BCL2-like 1 gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20200310 MGI PMID:18566418 1552009 Bcl2l1 BCL2-like 1 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20200310 MGI PMID:17382885 1552009 Bcl2l1 BCL2-like 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200310 MGI PMID:12093873 1552009 Bcl2l1 BCL2-like 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200310 MGI PMID:10894153 1552009 Bcl2l1 BCL2-like 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:15905539 1552009 Bcl2l1 BCL2-like 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:18566418 1552009 Bcl2l1 BCL2-like 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:12093873 1552009 Bcl2l1 BCL2-like 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:10894153 1552009 Bcl2l1 BCL2-like 1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20200310 MGI PMID:17382885 1552009 Bcl2l1 BCL2-like 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20200310 MGI PMID:17382885 1552009 Bcl2l1 BCL2-like 1 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20200310 MGI PMID:16033881 1552009 Bcl2l1 BCL2-like 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:11150333 1552009 Bcl2l1 BCL2-like 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:9096145 1552009 Bcl2l1 BCL2-like 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:11150333 1552009 Bcl2l1 BCL2-like 1 gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20200310 MGI PMID:12093873 1552009 Bcl2l1 BCL2-like 1 gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:12093873 1552009 Bcl2l1 BCL2-like 1 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:17382885 1552009 Bcl2l1 BCL2-like 1 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20200310 MGI PMID:10894153 1552009 Bcl2l1 BCL2-like 1 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20200310 MGI PMID:12665473 1552009 Bcl2l1 BCL2-like 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:20929728 1552009 Bcl2l1 BCL2-like 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20200310 MGI PMID:12093873 1552009 Bcl2l1 BCL2-like 1 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19209227 1552009 Bcl2l1 BCL2-like 1 gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:12665473 1552009 Bcl2l1 BCL2-like 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9096145 1552009 Bcl2l1 BCL2-like 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17382885 1552009 Bcl2l1 BCL2-like 1 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10894153 1552009 Bcl2l1 BCL2-like 1 gene MP:0020543 decreased substantia nigra size IAGP N RGD:5509061 20200310 MGI PMID:16033881 1552009 Bcl2l1 BCL2-like 1 gene MP:0030578 decreased keratinocyte adhesion IAGP N RGD:5509061 20200310 MGI PMID:12665473 1552011 Pitpnc1 phosphatidylinositol transfer protein, cytoplasmic 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20230601 MGI 1552011 Pitpnc1 phosphatidylinositol transfer protein, cytoplasmic 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1552011 Pitpnc1 phosphatidylinositol transfer protein, cytoplasmic 1 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 1552011 Pitpnc1 phosphatidylinositol transfer protein, cytoplasmic 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1552011 Pitpnc1 phosphatidylinositol transfer protein, cytoplasmic 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20230601 MGI 1552011 Pitpnc1 phosphatidylinositol transfer protein, cytoplasmic 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20230601 MGI 1552011 Pitpnc1 phosphatidylinositol transfer protein, cytoplasmic 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230601 MGI 1552011 Pitpnc1 phosphatidylinositol transfer protein, cytoplasmic 1 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20230601 MGI 1552013 Smyd2 SET and MYND domain containing 2 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20141003 MGI 1552013 Smyd2 SET and MYND domain containing 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1552014 Prrg4 proline rich Gla (G-carboxyglutamic acid) 4 (transmembrane) gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1552014 Prrg4 proline rich Gla (G-carboxyglutamic acid) 4 (transmembrane) gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1552014 Prrg4 proline rich Gla (G-carboxyglutamic acid) 4 (transmembrane) gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20230601 MGI 1552014 Prrg4 proline rich Gla (G-carboxyglutamic acid) 4 (transmembrane) gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1552015 Kcnip4 Kv channel interacting protein 4 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1552019 Ssr3 signal sequence receptor, gamma gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:21246656 1552019 Ssr3 signal sequence receptor, gamma gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:21246656 1552019 Ssr3 signal sequence receptor, gamma gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:21246656 1552019 Ssr3 signal sequence receptor, gamma gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21246656 1552019 Ssr3 signal sequence receptor, gamma gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:21246656 1552019 Ssr3 signal sequence receptor, gamma gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:21246656 1552019 Ssr3 signal sequence receptor, gamma gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21246656 1552019 Ssr3 signal sequence receptor, gamma gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:21246656 1552019 Ssr3 signal sequence receptor, gamma gene MP:0009658 increased placenta apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21246656 1552019 Ssr3 signal sequence receptor, gamma gene MP:0010038 abnormal placenta physiology IAGP N RGD:5509061 20141003 MGI PMID:21246656 1552019 Ssr3 signal sequence receptor, gamma gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21246656 1552019 Ssr3 signal sequence receptor, gamma gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20141003 MGI PMID:21246656 1552021 Dohh deoxyhypusine hydroxylase/monooxygenase gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20200310 MGI PMID:24832488 1552021 Dohh deoxyhypusine hydroxylase/monooxygenase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:26037925 1552021 Dohh deoxyhypusine hydroxylase/monooxygenase gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20200310 MGI PMID:26037925 1552021 Dohh deoxyhypusine hydroxylase/monooxygenase gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20200310 MGI PMID:26037925 1552021 Dohh deoxyhypusine hydroxylase/monooxygenase gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:26037925 1552021 Dohh deoxyhypusine hydroxylase/monooxygenase gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20200310 MGI PMID:26037925 1552021 Dohh deoxyhypusine hydroxylase/monooxygenase gene MP:0005150 cachexia IAGP N RGD:5509061 20200310 MGI PMID:26037925 1552021 Dohh deoxyhypusine hydroxylase/monooxygenase gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20200310 MGI PMID:26037925 1552021 Dohh deoxyhypusine hydroxylase/monooxygenase gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:24832488 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210520 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210520 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1552022 Disp3 dispatched RND transporter family member 3 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210128 MGI 1552024 Taar5 trace amine-associated receptor 5 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:22837392 1552025 Syt9 synaptotagmin IX gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1552025 Syt9 synaptotagmin IX gene MP:0001891 hydrocephaly IEA N RGD:5509061 20210826 MGI 1552025 Syt9 synaptotagmin IX gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1552027 Ep300 E1A binding protein p300 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18684867 1552027 Ep300 E1A binding protein p300 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0000296 absent trabeculae carneae IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:16237459 1552027 Ep300 E1A binding protein p300 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:16428436 1552027 Ep300 E1A binding protein p300 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:12384703 1552027 Ep300 E1A binding protein p300 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16428436 1552027 Ep300 E1A binding protein p300 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:14517256 1552027 Ep300 E1A binding protein p300 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12384703 1552027 Ep300 E1A binding protein p300 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16237459 1552027 Ep300 E1A binding protein p300 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12384703 1552027 Ep300 E1A binding protein p300 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:14517256 1552027 Ep300 E1A binding protein p300 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16237459 1552027 Ep300 E1A binding protein p300 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18684867 1552027 Ep300 E1A binding protein p300 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:14517256 1552027 Ep300 E1A binding protein p300 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:16237459 1552027 Ep300 E1A binding protein p300 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141225 MGI 1552027 Ep300 E1A binding protein p300 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18684867 1552027 Ep300 E1A binding protein p300 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12384703 1552027 Ep300 E1A binding protein p300 gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12384703 1552027 Ep300 E1A binding protein p300 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:12384703 1552027 Ep300 E1A binding protein p300 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20180118 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:14517256 1552027 Ep300 E1A binding protein p300 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:18684867 1552027 Ep300 E1A binding protein p300 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18684867 1552027 Ep300 E1A binding protein p300 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18684867 1552027 Ep300 E1A binding protein p300 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18684867 1552027 Ep300 E1A binding protein p300 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18684867 1552027 Ep300 E1A binding protein p300 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16428436 1552027 Ep300 E1A binding protein p300 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16428436 1552027 Ep300 E1A binding protein p300 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16428436 1552027 Ep300 E1A binding protein p300 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:12384703 1552027 Ep300 E1A binding protein p300 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:18684867 1552027 Ep300 E1A binding protein p300 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:16237459 1552027 Ep300 E1A binding protein p300 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:16428436 1552027 Ep300 E1A binding protein p300 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16428436 1552027 Ep300 E1A binding protein p300 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0008188 abnormal transitional stage B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0008240 abnormal spleen marginal zone macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12384703 1552027 Ep300 E1A binding protein p300 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18684867 1552027 Ep300 E1A binding protein p300 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:14517256 1552027 Ep300 E1A binding protein p300 gene MP:0010138 arteritis IAGP N RGD:5509061 20141003 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0010500 myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0010592 abnormal atrioventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12384703 1552027 Ep300 E1A binding protein p300 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16237459 1552027 Ep300 E1A binding protein p300 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14517256 1552027 Ep300 E1A binding protein p300 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14517256 1552027 Ep300 E1A binding protein p300 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16237459 1552027 Ep300 E1A binding protein p300 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14517256 1552027 Ep300 E1A binding protein p300 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:9590171 1552027 Ep300 E1A binding protein p300 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:14517255 1552027 Ep300 E1A binding protein p300 gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:17513743 1552027 Ep300 E1A binding protein p300 gene MP:0031590 abnormal epicardium development IAGP N RGD:5509061 20240229 MGI PMID:14517255 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0000706 small thymus IAGP N RGD:5509061 20210722 MGI PMID:28333124 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20210722 MGI PMID:28333124 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20210722 MGI PMID:28333124 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20210722 MGI PMID:28333124 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20210617 MGI PMID:31883536 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20210722 MGI PMID:28333124 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20210722 MGI PMID:28333124 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20210617 MGI PMID:31883536 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20210722 MGI PMID:28333124 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20210617 MGI PMID:31883536 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20210617 MGI PMID:31883536 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20210722 MGI PMID:28333124 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20210617 MGI PMID:31883536 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20210722 MGI PMID:28333124 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20210617 MGI PMID:31883536 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20210722 MGI PMID:28333124 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IAGP N RGD:5509061 20210722 MGI PMID:28333124 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0013772 increased effector memory T-helper cell number IAGP N RGD:5509061 20210722 MGI PMID:28333124 1552028 Bcap31 B cell receptor associated protein 31 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20210617 MGI PMID:31883536 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20371805 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:20371805 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20231455 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:20231455 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:20231455 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20231455 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20231455 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20371805 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20231455 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20371805 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20371805 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:20371805 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20371805 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210128 MGI 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20231455 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:20231455 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 1552030 Sptbn2 spectrin beta, non-erythrocytic 2 gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:20371805 1552032 Pfkfb4 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20230601 MGI 1552032 Pfkfb4 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1552032 Pfkfb4 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 1552035 Trmt61a tRNA methyltransferase 61A gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20231109 MGI PMID:36138184 1552035 Trmt61a tRNA methyltransferase 61A gene MP:0002816 colitis IAGP N RGD:5509061 20231109 MGI PMID:36138184 1552035 Trmt61a tRNA methyltransferase 61A gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:36138184 1552035 Trmt61a tRNA methyltransferase 61A gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20231109 MGI PMID:36138184 1552035 Trmt61a tRNA methyltransferase 61A gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20231109 MGI PMID:36138184 1552035 Trmt61a tRNA methyltransferase 61A gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20231109 MGI PMID:36138184 1552035 Trmt61a tRNA methyltransferase 61A gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20231109 MGI PMID:36138184 1552035 Trmt61a tRNA methyltransferase 61A gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20231109 MGI PMID:36138184 1552037 Capn11 calpain 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1552037 Capn11 calpain 11 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20201022 MGI 1552038 Prss59 protease, serine 59 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20210415 MGI PMID:32020604 1552038 Prss59 protease, serine 59 gene MP:0001925 male infertility IAGP N RGD:5509061 20210415 MGI PMID:32020604 1552038 Prss59 protease, serine 59 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20210415 MGI PMID:32020604 1552040 Agbl2 ATP/GTP binding protein-like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:25103237 1552040 Agbl2 ATP/GTP binding protein-like 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:22573622 1552041 Tcf21 transcription factor 21 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:22573622 1552041 Tcf21 transcription factor 21 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:10944221 1552041 Tcf21 transcription factor 21 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:22792366 1552041 Tcf21 transcription factor 21 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:22792366 1552041 Tcf21 transcription factor 21 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:10944221 1552041 Tcf21 transcription factor 21 gene MP:0000692 small spleen IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:12493912 1552041 Tcf21 transcription factor 21 gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:15289436 1552041 Tcf21 transcription factor 21 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:15289436 1552041 Tcf21 transcription factor 21 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10944221 1552041 Tcf21 transcription factor 21 gene MP:0001184 absent pulmonary alveoli IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0001184 absent pulmonary alveoli IAGP N RGD:5509061 20141003 MGI PMID:10944221 1552041 Tcf21 transcription factor 21 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10944221 1552041 Tcf21 transcription factor 21 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0001785 edema IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:15289436 1552041 Tcf21 transcription factor 21 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10944221 1552041 Tcf21 transcription factor 21 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22792366 1552041 Tcf21 transcription factor 21 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22792366 1552041 Tcf21 transcription factor 21 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22792366 1552041 Tcf21 transcription factor 21 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:22792366 1552041 Tcf21 transcription factor 21 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20150205 MGI PMID:24904088 1552041 Tcf21 transcription factor 21 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20150205 MGI PMID:24904088 1552041 Tcf21 transcription factor 21 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12493912 1552041 Tcf21 transcription factor 21 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21432986 1552041 Tcf21 transcription factor 21 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:22573622 1552041 Tcf21 transcription factor 21 gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20150205 MGI PMID:24904088 1552041 Tcf21 transcription factor 21 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20150205 MGI PMID:24904088 1552041 Tcf21 transcription factor 21 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0002989 small kidney IAGP N RGD:5509061 20150205 MGI PMID:24904088 1552041 Tcf21 transcription factor 21 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:15289436 1552041 Tcf21 transcription factor 21 gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10944221 1552041 Tcf21 transcription factor 21 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22792366 1552041 Tcf21 transcription factor 21 gene MP:0003605 fused kidneys IAGP N RGD:5509061 20141003 MGI PMID:22792366 1552041 Tcf21 transcription factor 21 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:22792366 1552041 Tcf21 transcription factor 21 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:10944221 1552041 Tcf21 transcription factor 21 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:12493912 1552041 Tcf21 transcription factor 21 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20141003 MGI PMID:22792366 1552041 Tcf21 transcription factor 21 gene MP:0004234 abnormal masticatory muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12493912 1552041 Tcf21 transcription factor 21 gene MP:0004236 absent masseter muscle IAGP N RGD:5509061 20141003 MGI PMID:12493912 1552041 Tcf21 transcription factor 21 gene MP:0004237 abnormal pterygoid muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12493912 1552041 Tcf21 transcription factor 21 gene MP:0004238 absent pterygoid muscle IAGP N RGD:5509061 20141003 MGI PMID:12493912 1552041 Tcf21 transcription factor 21 gene MP:0004240 absent temporalis muscle IAGP N RGD:5509061 20141003 MGI PMID:12493912 1552041 Tcf21 transcription factor 21 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:22792366 1552041 Tcf21 transcription factor 21 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10944221 1552041 Tcf21 transcription factor 21 gene MP:0004969 pale kidney IAGP N RGD:5509061 20150205 MGI PMID:24904088 1552041 Tcf21 transcription factor 21 gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20150205 MGI PMID:24904088 1552041 Tcf21 transcription factor 21 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:22573622 1552041 Tcf21 transcription factor 21 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20150205 MGI PMID:24904088 1552041 Tcf21 transcription factor 21 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20150205 MGI PMID:24904088 1552041 Tcf21 transcription factor 21 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20150205 MGI PMID:24904088 1552041 Tcf21 transcription factor 21 gene MP:0005652 sex reversal IAGP N RGD:5509061 20141003 MGI PMID:15289436 1552041 Tcf21 transcription factor 21 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0006419 disorganized testis cords IAGP N RGD:5509061 20141003 MGI PMID:15289436 1552041 Tcf21 transcription factor 21 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20150205 MGI PMID:24904088 1552041 Tcf21 transcription factor 21 gene MP:0008727 increased heart right atrium size IAGP N RGD:5509061 20141003 MGI PMID:22573622 1552041 Tcf21 transcription factor 21 gene MP:0009323 abnormal spleen development IAGP N RGD:5509061 20141003 MGI PMID:10944221 1552041 Tcf21 transcription factor 21 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20150205 MGI PMID:24904088 1552041 Tcf21 transcription factor 21 gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:12493912 1552041 Tcf21 transcription factor 21 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:12493912 1552041 Tcf21 transcription factor 21 gene MP:0010812 absent type II pneumocytes IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0010911 abnormal pulmonary acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0010976 small lung lobe IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0010981 abnormal branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0010985 abnormal kidney mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10944221 1552041 Tcf21 transcription factor 21 gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0011038 impaired branching involved in alveolar sac morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10944221 1552041 Tcf21 transcription factor 21 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12493912 1552041 Tcf21 transcription factor 21 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21432986 1552041 Tcf21 transcription factor 21 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1552041 Tcf21 transcription factor 21 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0011298 ureter hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22792366 1552041 Tcf21 transcription factor 21 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0011321 abnormal peritubular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0011351 absent proximal convoluted tubule brush border IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20141003 MGI PMID:10944221 1552041 Tcf21 transcription factor 21 gene MP:0011727 ectopic ovary IAGP N RGD:5509061 20141003 MGI PMID:15289436 1552041 Tcf21 transcription factor 21 gene MP:0011760 abnormal ureteric bud tip morphology IAGP N RGD:5509061 20141003 MGI PMID:10572052 1552041 Tcf21 transcription factor 21 gene MP:0012515 abnormal heart apex morphology IAGP N RGD:5509061 20141003 MGI PMID:22573622 1552041 Tcf21 transcription factor 21 gene MP:0020491 abnormal ovary topology IAGP N RGD:5509061 20171026 MGI PMID:15289436 1552044 Lysmd3 LysM, putative peptidoglycan-binding, domain containing 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20181220 MGI PMID:29496999 1552045 Ica1l islet cell autoantigen 1-like gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1552045 Ica1l islet cell autoantigen 1-like gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20161117 MGI PMID:26306493 1552045 Ica1l islet cell autoantigen 1-like gene MP:0001925 male infertility IAGP N RGD:5509061 20161117 MGI PMID:26306493 1552045 Ica1l islet cell autoantigen 1-like gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20161117 MGI PMID:26306493 1552045 Ica1l islet cell autoantigen 1-like gene MP:0001935 decreased litter size IAGP N RGD:5509061 20161117 MGI PMID:26306493 1552045 Ica1l islet cell autoantigen 1-like gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1552045 Ica1l islet cell autoantigen 1-like gene MP:0002686 globozoospermia IAGP N RGD:5509061 20161117 MGI PMID:26306493 1552045 Ica1l islet cell autoantigen 1-like gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20161117 MGI PMID:26306493 1552045 Ica1l islet cell autoantigen 1-like gene MP:0008839 absent acrosome IAGP N RGD:5509061 20161117 MGI PMID:26306493 1552045 Ica1l islet cell autoantigen 1-like gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20161117 MGI PMID:26306493 1552045 Ica1l islet cell autoantigen 1-like gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20161117 MGI PMID:26306493 1552045 Ica1l islet cell autoantigen 1-like gene MP:0009476 enlarged cecum IEA N RGD:5509061 20181227 MGI 1552045 Ica1l islet cell autoantigen 1-like gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20161117 MGI PMID:26306493 1552047 Cops4 COP9 signalosome subunit 4 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1552047 Cops4 COP9 signalosome subunit 4 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20141003 MGI 1552047 Cops4 COP9 signalosome subunit 4 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20141003 MGI 1552047 Cops4 COP9 signalosome subunit 4 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160804 MGI 1552047 Cops4 COP9 signalosome subunit 4 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 1552050 Tchhl1 trichohyalin-like 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20221215 MGI 1552051 Clca2 chloride channel accessory 2 gene MP:0000599 enlarged liver IEA N RGD:5509061 20111116 MGI 1552051 Clca2 chloride channel accessory 2 gene MP:0000607 abnormal hepatocyte morphology IEA N RGD:5509061 20111116 MGI 1552051 Clca2 chloride channel accessory 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1552051 Clca2 chloride channel accessory 2 gene MP:0001147 small testis IEA N RGD:5509061 20230119 MGI 1552051 Clca2 chloride channel accessory 2 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1552051 Clca2 chloride channel accessory 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 1552051 Clca2 chloride channel accessory 2 gene MP:0001655 multifocal hepatic necrosis IEA N RGD:5509061 20111116 MGI 1552051 Clca2 chloride channel accessory 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1552051 Clca2 chloride channel accessory 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1552051 Clca2 chloride channel accessory 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1552051 Clca2 chloride channel accessory 2 gene MP:0002981 increased liver weight IEA N RGD:5509061 20111116 MGI 1552051 Clca2 chloride channel accessory 2 gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:17549259 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:18463233 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:19319191 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20200310 MGI PMID:15907819 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20200310 MGI PMID:12068289 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:12032136 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:12068289 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20200310 MGI PMID:12068289 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20200310 MGI PMID:12860835 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20200310 MGI PMID:12860835 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:15907819 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:15907819 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:12068289 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200310 MGI PMID:18463233 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20200310 MGI PMID:15907819 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:17549259 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20200310 MGI PMID:15907819 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0002871 albuminuria IAGP N RGD:5509061 20200310 MGI PMID:18431508 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:18463233 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20200310 MGI PMID:16326714 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20200310 MGI PMID:19319191 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:18431508 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0003718 maternal effect IAGP N RGD:5509061 20200310 MGI PMID:25590242 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:19319191 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20200310 MGI PMID:15907819 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0003948 abnormal gas homeostasis IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20200310 MGI PMID:17549259 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0004149 increased bone strength IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20200310 MGI PMID:12032136 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20200310 MGI PMID:12138120 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20200310 MGI PMID:24531262 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0004892 increased adiponectin level IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005114 premature hair loss IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:24531262 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:12032136 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:16326714 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200310 MGI PMID:12032136 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200310 MGI PMID:12068289 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200310 MGI PMID:17693256 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20200310 MGI PMID:24531262 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005413 vascular restenosis IAGP N RGD:5509061 20200310 MGI PMID:12138120 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:15907819 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20231207 MGI 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005605 increased bone mass IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005630 increased lung weight IAGP N RGD:5509061 20200310 MGI PMID:19319191 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:12860835 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20200310 MGI PMID:15907819 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20200310 MGI PMID:12860835 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20200310 MGI PMID:18431508 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:15907819 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20200310 MGI PMID:15907819 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19319191 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20200310 MGI PMID:24531262 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0011016 increased core body temperature IAGP N RGD:5509061 20200310 MGI PMID:24531262 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19319191 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0011939 increased food intake IAGP N RGD:5509061 20200310 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0011940 decreased food intake IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0014174 decreased fatty acid beta-oxidation IAGP N RGD:5509061 20200310 MGI PMID:12151381 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0020318 increased vascular endothelial cell adhesion IAGP N RGD:5509061 20200310 MGI PMID:17549259 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20200310 MGI PMID:24531262 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0030770 increased urine adrenaline level IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20200310 MGI PMID:17549259 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20200310 MGI PMID:17693256 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20200310 MGI PMID:19319191 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0030984 increased circulating osteocalcin level IAGP N RGD:5509061 20200310 MGI PMID:23684624 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0031269 increased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:16595853 1552054 Adipoq adiponectin, C1Q and collagen domain containing gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15907819 1552056 Lipm lipase, family member M gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20221215 MGI 1552056 Lipm lipase, family member M gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1552058 Ift172 intraflagellar transport 172 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200310 MGI 1552058 Ift172 intraflagellar transport 172 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20200310 MGI 1552058 Ift172 intraflagellar transport 172 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0000445 short snout IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:19521792 1552058 Ift172 intraflagellar transport 172 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:19521792 1552058 Ift172 intraflagellar transport 172 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:15755804 1552058 Ift172 intraflagellar transport 172 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20200310 MGI PMID:14603322 1552058 Ift172 intraflagellar transport 172 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20200310 MGI PMID:19666503 1552058 Ift172 intraflagellar transport 172 gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:14603322 1552058 Ift172 intraflagellar transport 172 gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:16061793 1552058 Ift172 intraflagellar transport 172 gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200310 MGI PMID:16061793 1552058 Ift172 intraflagellar transport 172 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20200310 MGI PMID:15755804 1552058 Ift172 intraflagellar transport 172 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200310 MGI PMID:29659833 1552058 Ift172 intraflagellar transport 172 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:19521792 1552058 Ift172 intraflagellar transport 172 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20200310 MGI 1552058 Ift172 intraflagellar transport 172 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20200310 MGI PMID:15755804 1552058 Ift172 intraflagellar transport 172 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0001726 abnormal allantois morphology IEA N RGD:5509061 20200310 MGI 1552058 Ift172 intraflagellar transport 172 gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20200310 MGI PMID:20511334 1552058 Ift172 intraflagellar transport 172 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20200402 MGI 1552058 Ift172 intraflagellar transport 172 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:19521792 1552058 Ift172 intraflagellar transport 172 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:19666503 1552058 Ift172 intraflagellar transport 172 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0002764 short tibia IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0002765 short fibula IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20200310 MGI 1552058 Ift172 intraflagellar transport 172 gene MP:0003109 short femur IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0003130 anal atresia IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0003276 esophageal atresia IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20200310 MGI 1552058 Ift172 intraflagellar transport 172 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20200310 MGI PMID:29659833 1552058 Ift172 intraflagellar transport 172 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1552058 Ift172 intraflagellar transport 172 gene MP:0004131 abnormal motile primary cilium morphology IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20200310 MGI PMID:14603322 1552058 Ift172 intraflagellar transport 172 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20200310 MGI PMID:14603322 1552058 Ift172 intraflagellar transport 172 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20200310 MGI PMID:16061793 1552058 Ift172 intraflagellar transport 172 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0004351 short humerus IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0004355 short radius IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0004359 short ulna IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200310 MGI PMID:29659833 1552058 Ift172 intraflagellar transport 172 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20200310 MGI PMID:29659833 1552058 Ift172 intraflagellar transport 172 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20200310 MGI PMID:29659833 1552058 Ift172 intraflagellar transport 172 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200310 MGI PMID:29659833 1552058 Ift172 intraflagellar transport 172 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20200310 MGI PMID:20511334 1552058 Ift172 intraflagellar transport 172 gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20200310 MGI PMID:20511334 1552058 Ift172 intraflagellar transport 172 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20200310 MGI PMID:20511334 1552058 Ift172 intraflagellar transport 172 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201022 MGI 1552058 Ift172 intraflagellar transport 172 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20200310 MGI PMID:20511334 1552058 Ift172 intraflagellar transport 172 gene MP:0010881 esophagus hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0010884 esophagus stenosis IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19521792 1552058 Ift172 intraflagellar transport 172 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:14603322 1552058 Ift172 intraflagellar transport 172 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15755804 1552058 Ift172 intraflagellar transport 172 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16061793 1552058 Ift172 intraflagellar transport 172 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18930042 1552058 Ift172 intraflagellar transport 172 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552058 Ift172 intraflagellar transport 172 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20200310 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200310 MGI PMID:29659833 1552058 Ift172 intraflagellar transport 172 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200310 MGI PMID:29659833 1552058 Ift172 intraflagellar transport 172 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:18488998 1552058 Ift172 intraflagellar transport 172 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:21653639 1552058 Ift172 intraflagellar transport 172 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1552058 Ift172 intraflagellar transport 172 gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20200310 MGI PMID:29659833 1552058 Ift172 intraflagellar transport 172 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20220210 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220317 MGI PMID:31958312 1552058 Ift172 intraflagellar transport 172 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20220428 MGI PMID:31958312 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20230727 MGI PMID:36306217 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20230622 MGI PMID:34623009 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20230727 MGI PMID:36306217 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20230622 MGI PMID:34623009 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20230727 MGI PMID:36306217 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20230622 MGI PMID:34623009 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20230727 MGI PMID:36306217 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230622 MGI PMID:34623009 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230727 MGI PMID:36306217 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20230727 MGI PMID:36306217 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230622 MGI PMID:34623009 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230727 MGI PMID:36306217 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20230727 MGI PMID:36306217 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20230622 MGI PMID:34623009 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20230727 MGI PMID:36306217 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20230622 MGI PMID:34623009 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20230727 MGI PMID:36306217 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20230622 MGI PMID:34623009 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20230727 MGI PMID:36306217 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20230727 MGI PMID:36306217 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20230727 MGI PMID:36306217 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20230622 MGI PMID:34623009 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20230727 MGI PMID:36306217 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20230727 MGI PMID:36306217 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20230622 MGI PMID:34623009 1552060 Tssk3 testis-specific serine kinase 3 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20230622 MGI PMID:34623009 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19330010 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18843253 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18165355 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22577176 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:16275892 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:9362535 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:17351623 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9362535 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9362535 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10843684 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20220811 MGI 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:19330010 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:10751350 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0001655 multifocal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:9362535 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:9362535 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:10843684 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9366570 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17351623 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0001987 alcohol preference IAGP N RGD:5509061 20141003 MGI PMID:16105698 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23986513 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17351623 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12504109 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:10438957 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9362535 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17257744 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18843253 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21060874 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:23986513 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:14566334 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002570 alcohol aversion IAGP N RGD:5509061 20141003 MGI PMID:16105698 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002620 abnormal monocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17364026 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:10438957 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:16105698 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:10751350 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20211021 MGI PMID:31813573 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:10843684 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:11591787 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:21458307 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:17351623 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:17257744 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:16105698 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:16105698 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:16275892 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11591787 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17351623 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12504109 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17351623 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:18843253 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:19641140 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:22190646 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:9362535 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:9366570 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:9732872 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:14566334 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:22577176 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10751350 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10751350 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20231207 MGI 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:18843253 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:11015448 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21060874 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:12065319 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0004983 abnormal osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:19330010 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:19330010 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9362535 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10843684 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:22577176 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:10843684 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:11591787 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11015448 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005098 abnormal optic choroid morphology IAGP N RGD:5509061 20141003 MGI PMID:14566334 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20211021 MGI PMID:31813573 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21779871 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14566334 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:14566334 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12504109 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:23986513 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23986513 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18165355 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9732872 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16444257 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005546 choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:14566334 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:18843253 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10438957 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20231207 MGI 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21779871 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0006187 retina deposits IAGP N RGD:5509061 20141003 MGI PMID:14566334 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0006238 abnormal choriocapillaris morphology IAGP N RGD:5509061 20141003 MGI PMID:14566334 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0006315 abnormal urine protein level IAGP N RGD:5509061 20141003 MGI PMID:23986513 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10843684 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10843684 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20150924 MGI PMID:23168837 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:19330010 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:14566334 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:14566334 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:10843684 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20483766 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:10751350 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10751350 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11015448 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11591787 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9366570 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:9366570 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:11015448 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:19641140 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:9366570 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20141003 MGI PMID:14566334 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10751350 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23986513 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11015448 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:19330010 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:16275892 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0009878 decreased susceptibility to bone fracture IAGP N RGD:5509061 20141003 MGI PMID:19330010 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0010119 abnormal bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19330010 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0010740 abnormal dendritic cell chemotaxis IAGP N RGD:5509061 20150924 MGI PMID:23168837 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:9366570 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:19330010 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:19330010 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:16105698 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0013648 increased CD11b-high dendritic cell number IAGP N RGD:5509061 20150924 MGI PMID:23168837 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0013649 decreased CD11b-high dendritic cell number IAGP N RGD:5509061 20150924 MGI PMID:23168837 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:19357362 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:19079579 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200514 MGI PMID:11591787 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:21779871 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:11591787 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0031054 bronchiolitis IAGP N RGD:5509061 20200709 MGI PMID:19079579 1552061 Ccr2 C-C motif chemokine receptor 2 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:14566334 1552063 Kif15 kinesin family member 15 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20231109 MGI PMID:36934586 1552063 Kif15 kinesin family member 15 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20231109 MGI PMID:36934586 1552063 Kif15 kinesin family member 15 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20231109 MGI PMID:36934586 1552063 Kif15 kinesin family member 15 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20231109 MGI PMID:36934586 1552063 Kif15 kinesin family member 15 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20231109 MGI PMID:36934586 1552063 Kif15 kinesin family member 15 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20231109 MGI PMID:36934586 1552063 Kif15 kinesin family member 15 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20231109 MGI PMID:36934586 1552066 Tmtc2 transmembrane and tetratricopeptide repeat containing 2 gene MP:0009453 enhanced contextual conditioning behavior IEA N RGD:5509061 20230601 MGI 1552067 Spink2 serine peptidase inhibitor, Kazal type 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21705336 1552067 Spink2 serine peptidase inhibitor, Kazal type 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:21705336 1552067 Spink2 serine peptidase inhibitor, Kazal type 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:21705336 1552067 Spink2 serine peptidase inhibitor, Kazal type 2 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1552067 Spink2 serine peptidase inhibitor, Kazal type 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21705336 1552067 Spink2 serine peptidase inhibitor, Kazal type 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21705336 1552067 Spink2 serine peptidase inhibitor, Kazal type 2 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20231207 MGI 1552067 Spink2 serine peptidase inhibitor, Kazal type 2 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170105 MGI 1552067 Spink2 serine peptidase inhibitor, Kazal type 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21705336 1552067 Spink2 serine peptidase inhibitor, Kazal type 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20231207 MGI 1552067 Spink2 serine peptidase inhibitor, Kazal type 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21705336 1552067 Spink2 serine peptidase inhibitor, Kazal type 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21705336 1552067 Spink2 serine peptidase inhibitor, Kazal type 2 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21705336 1552067 Spink2 serine peptidase inhibitor, Kazal type 2 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:21705336 1552068 Kcne4 potassium voltage-gated channel, Isk-related subfamily, gene 4 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20211104 MGI PMID:26399785 1552068 Kcne4 potassium voltage-gated channel, Isk-related subfamily, gene 4 gene MP:0020345 abnormal myocardial fiber currents IAGP N RGD:5509061 20211104 MGI PMID:26399785 1552068 Kcne4 potassium voltage-gated channel, Isk-related subfamily, gene 4 gene MP:0020418 increased cardiac muscle relaxation IAGP N RGD:5509061 20211104 MGI PMID:26399785 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19879845 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000553 absent radius IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:19879845 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19879845 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20221124 MGI PMID:31300413 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20221124 MGI PMID:31300413 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23267101 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:23267101 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23267101 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23267101 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:19879845 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:19879845 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23267101 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20221124 MGI PMID:31300413 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20221124 MGI PMID:31300413 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20221124 MGI PMID:31300413 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0003655 absent pancreas IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:23267101 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20221124 MGI PMID:31300413 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23267101 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:15314648 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0006292 abnormal nasal placode morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0006339 abnormal third pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0006339 abnormal third pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0006340 abnormal fourth pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0006347 abnormal sixth pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:23267101 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23267101 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0009111 pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0009705 abnormal midgut morphology IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0009806 abnormal otic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0009806 abnormal otic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0009806 abnormal otic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20221124 MGI PMID:31300413 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221124 MGI PMID:31300413 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221124 MGI PMID:31300413 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0009895 decreased palatine bone horizontal plate size IAGP N RGD:5509061 20221124 MGI PMID:31300413 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20221124 MGI PMID:31300413 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0010356 abnormal second pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0010642 absent third pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0010643 absent fourth pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0010643 absent fourth pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0010644 absent sixth pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0010707 decreased ventral retina size IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0010907 absent lung buds IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0011026 impaired branching involved in trachea morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0011233 abnormal vitamin A metabolism IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0011364 abnormal metanephros morphology IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0012247 absent cornea IAGP N RGD:5509061 20171019 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0012270 cardiac edema IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0013164 abnormal forelimb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0013166 small forelimb buds IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0013166 small forelimb buds IAGP N RGD:5509061 20141003 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:21930923 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0013817 absent nasal cavity IAGP N RGD:5509061 20171019 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0014291 decreased autopod size IAGP N RGD:5509061 20230824 MGI PMID:17473173 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0020350 fused pharyngeal arches IAGP N RGD:5509061 20160915 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0020350 fused pharyngeal arches IAGP N RGD:5509061 20160915 MGI PMID:22319578 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0030250 frontonasal prominence hypoplasia IAGP N RGD:5509061 20171019 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0030334 absent sixth pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0030335 absent third pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:21305688 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221124 MGI PMID:31300413 1552069 Rdh10 retinol dehydrogenase 10 (all-trans) gene MP:0031464 abnormal spontaneous fetal mouth movement IAGP N RGD:5509061 20230302 MGI PMID:31300413 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0001925 male infertility IAGP N RGD:5509061 20210415 MGI PMID:33536340 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0001925 male infertility IAGP N RGD:5509061 20211209 MGI PMID:32976492 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20211209 MGI PMID:32976492 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20211209 MGI PMID:32976492 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20211209 MGI PMID:32976492 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210415 MGI PMID:33536340 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20211209 MGI PMID:32976492 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20210415 MGI PMID:33536340 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20211209 MGI PMID:32976492 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20210415 MGI PMID:33536340 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20211209 MGI PMID:32976492 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20211209 MGI PMID:32976492 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20211209 MGI PMID:32976492 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20211209 MGI PMID:32976492 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:32976492 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20211209 MGI PMID:32976492 1552071 Tbc1d21 TBC1 domain family, member 21 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220811 MGI PMID:32976492 1552078 Kif2b kinesin family member 2B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1552080 Vps26a VPS26 retromer complex component A gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:16214895 1552080 Vps26a VPS26 retromer complex component A gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16214895 1552080 Vps26a VPS26 retromer complex component A gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:1879343 1552080 Vps26a VPS26 retromer complex component A gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:1879343 1552080 Vps26a VPS26 retromer complex component A gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:1879343 1552080 Vps26a VPS26 retromer complex component A gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16214895 1552080 Vps26a VPS26 retromer complex component A gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:1879343 1552080 Vps26a VPS26 retromer complex component A gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:1879343 1552080 Vps26a VPS26 retromer complex component A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16214895 1552080 Vps26a VPS26 retromer complex component A gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:1879343 1552080 Vps26a VPS26 retromer complex component A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16214895 1552080 Vps26a VPS26 retromer complex component A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:1879343 1552080 Vps26a VPS26 retromer complex component A gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16214895 1552080 Vps26a VPS26 retromer complex component A gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16214895 1552080 Vps26a VPS26 retromer complex component A gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16214895 1552080 Vps26a VPS26 retromer complex component A gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1879343 1552080 Vps26a VPS26 retromer complex component A gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16214895 1552084 Mapkapk3 mitogen-activated protein kinase-activated protein kinase 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1552084 Mapkapk3 mitogen-activated protein kinase-activated protein kinase 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1552084 Mapkapk3 mitogen-activated protein kinase-activated protein kinase 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1552084 Mapkapk3 mitogen-activated protein kinase-activated protein kinase 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1552084 Mapkapk3 mitogen-activated protein kinase-activated protein kinase 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1552084 Mapkapk3 mitogen-activated protein kinase-activated protein kinase 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1552084 Mapkapk3 mitogen-activated protein kinase-activated protein kinase 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1552084 Mapkapk3 mitogen-activated protein kinase-activated protein kinase 3 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200310 MGI PMID:17030606 1552087 Zfp219 zinc finger protein 219 gene MP:0001759 increased urine glucose level IEA N RGD:5509061 20211021 MGI 1552087 Zfp219 zinc finger protein 219 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20210520 MGI 1552087 Zfp219 zinc finger protein 219 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1552092 Zbtb12 zinc finger and BTB domain containing 12 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210826 MGI 1552092 Zbtb12 zinc finger and BTB domain containing 12 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1552092 Zbtb12 zinc finger and BTB domain containing 12 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1552092 Zbtb12 zinc finger and BTB domain containing 12 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210520 MGI 1552092 Zbtb12 zinc finger and BTB domain containing 12 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20240523 MGI 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0009839 multiflagellated sperm IAGP N RGD:5509061 20220630 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:12556490 1552095 Gmcl1 germ cell-less, spermatogenesis associated 1 gene MP:0031408 multi-headed sperm IAGP N RGD:5509061 20220630 MGI PMID:12556490 1552096 Tnks2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16507984 1552096 Tnks2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16507985 1552096 Tnks2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18612384 1552096 Tnks2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210520 MGI 1552096 Tnks2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18612384 1552096 Tnks2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:18612384 1552096 Tnks2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:18612384 1552096 Tnks2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1552096 Tnks2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:18612384 1552096 Tnks2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1552096 Tnks2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16507985 1552096 Tnks2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18612384 1552096 Tnks2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2 gene MP:0012134 absent umbilical cord IAGP N RGD:5509061 20141003 MGI PMID:18612384 1552096 Tnks2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2 gene MP:0012301 absent umbilical cord blood vessels IAGP N RGD:5509061 20141003 MGI PMID:18612384 1552096 Tnks2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:18612384 1552098 Lrrc49 leucine rich repeat containing 49 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20200310 MGI 1552098 Lrrc49 leucine rich repeat containing 49 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552098 Lrrc49 leucine rich repeat containing 49 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20210128 MGI 1552099 Baz2a bromodomain adjacent to zinc finger domain, 2A gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 1552099 Baz2a bromodomain adjacent to zinc finger domain, 2A gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 1552099 Baz2a bromodomain adjacent to zinc finger domain, 2A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1552099 Baz2a bromodomain adjacent to zinc finger domain, 2A gene MP:0002989 small kidney IEA N RGD:5509061 20181227 MGI 1552099 Baz2a bromodomain adjacent to zinc finger domain, 2A gene MP:0004930 small epididymis IEA N RGD:5509061 20181227 MGI 1552099 Baz2a bromodomain adjacent to zinc finger domain, 2A gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1552099 Baz2a bromodomain adjacent to zinc finger domain, 2A gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20181227 MGI 1552099 Baz2a bromodomain adjacent to zinc finger domain, 2A gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1552100 Zfp260 zinc finger protein 260 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1552100 Zfp260 zinc finger protein 260 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1552100 Zfp260 zinc finger protein 260 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1552100 Zfp260 zinc finger protein 260 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1552100 Zfp260 zinc finger protein 260 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1552100 Zfp260 zinc finger protein 260 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1552100 Zfp260 zinc finger protein 260 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 1552100 Zfp260 zinc finger protein 260 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 1552102 Tns1 tensin 1 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20200310 MGI PMID:26301497 1552102 Tns1 tensin 1 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0000746 weakness IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0003606 kidney failure IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0004969 pale kidney IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0005526 decreased renal plasma flow rate IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0010614 abnormal mitral valve cusp morphology IAGP N RGD:5509061 20200310 MGI PMID:26301497 1552102 Tns1 tensin 1 gene MP:0011402 renal cast IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552102 Tns1 tensin 1 gene MP:0011534 granular kidney IAGP N RGD:5509061 20200310 MGI PMID:9087448 1552103 Ccdc25 coiled-coil domain containing 25 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1552103 Ccdc25 coiled-coil domain containing 25 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20201022 MGI PMID:32528174 1552103 Ccdc25 coiled-coil domain containing 25 gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1552103 Ccdc25 coiled-coil domain containing 25 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1552103 Ccdc25 coiled-coil domain containing 25 gene MP:0001333 absent optic nerve IEA N RGD:5509061 20210520 MGI 1552103 Ccdc25 coiled-coil domain containing 25 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1552103 Ccdc25 coiled-coil domain containing 25 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20220519 MGI 1552103 Ccdc25 coiled-coil domain containing 25 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1552103 Ccdc25 coiled-coil domain containing 25 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20220519 MGI 1552103 Ccdc25 coiled-coil domain containing 25 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20231207 MGI 1552103 Ccdc25 coiled-coil domain containing 25 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1552104 Hnrnpll heterogeneous nuclear ribonucleoprotein L-like gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:19100700 1552104 Hnrnpll heterogeneous nuclear ribonucleoprotein L-like gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:19100700 1552104 Hnrnpll heterogeneous nuclear ribonucleoprotein L-like gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:19100700 1552104 Hnrnpll heterogeneous nuclear ribonucleoprotein L-like gene MP:0010833 abnormal memory T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:19100700 1552109 Get1 guided entry of tail-anchored proteins factor 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200402 MGI 1552109 Get1 guided entry of tail-anchored proteins factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552109 Get1 guided entry of tail-anchored proteins factor 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1552109 Get1 guided entry of tail-anchored proteins factor 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1552114 Wdsub1 WD repeat, SAM and U-box domain containing 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20220811 MGI 1552114 Wdsub1 WD repeat, SAM and U-box domain containing 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20240523 MGI 1552114 Wdsub1 WD repeat, SAM and U-box domain containing 1 gene MP:0004357 long tibia IEA N RGD:5509061 20220519 MGI 1552114 Wdsub1 WD repeat, SAM and U-box domain containing 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1552114 Wdsub1 WD repeat, SAM and U-box domain containing 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1552114 Wdsub1 WD repeat, SAM and U-box domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552115 Smyd1 SET and MYND domain containing 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11923873 1552115 Smyd1 SET and MYND domain containing 1 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11923873 1552115 Smyd1 SET and MYND domain containing 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11923873 1552115 Smyd1 SET and MYND domain containing 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11923873 1552115 Smyd1 SET and MYND domain containing 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11923873 1552115 Smyd1 SET and MYND domain containing 1 gene MP:0010432 common ventricle IAGP N RGD:5509061 20141003 MGI PMID:11923873 1552115 Smyd1 SET and MYND domain containing 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11923873 1552116 Mapre3 microtubule-associated protein, RP/EB family, member 3 gene MP:0001619 abnormal vascular permeability IAGP N RGD:5509061 20160721 MGI PMID:26119739 1552116 Mapre3 microtubule-associated protein, RP/EB family, member 3 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20141003 MGI 1552118 Tspan8 tetraspanin 8 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 1552118 Tspan8 tetraspanin 8 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230119 MGI 1552118 Tspan8 tetraspanin 8 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1552118 Tspan8 tetraspanin 8 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230119 MGI 1552119 Dhx16 DEAH-box helicase 16 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1552119 Dhx16 DEAH-box helicase 16 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20211021 MGI 1552119 Dhx16 DEAH-box helicase 16 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230601 MGI 1552119 Dhx16 DEAH-box helicase 16 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552119 Dhx16 DEAH-box helicase 16 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1552120 Ghitm growth hormone inducible transmembrane protein gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20230323 MGI PMID:35715207 1552120 Ghitm growth hormone inducible transmembrane protein gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20230323 MGI PMID:35715207 1552120 Ghitm growth hormone inducible transmembrane protein gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20230323 MGI PMID:35715207 1552120 Ghitm growth hormone inducible transmembrane protein gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20230323 MGI PMID:35715207 1552120 Ghitm growth hormone inducible transmembrane protein gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:35715207 1552123 Srek1 splicing regulatory glutamine/lysine-rich protein 1 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1552123 Srek1 splicing regulatory glutamine/lysine-rich protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552126 Adad1 adenosine deaminase domain containing 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:15649457 1552126 Adad1 adenosine deaminase domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15649457 1552126 Adad1 adenosine deaminase domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20230803 MGI PMID:36698249 1552126 Adad1 adenosine deaminase domain containing 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20230803 MGI PMID:36698249 1552126 Adad1 adenosine deaminase domain containing 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15649457 1552126 Adad1 adenosine deaminase domain containing 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15649457 1552126 Adad1 adenosine deaminase domain containing 1 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20220519 MGI 1552126 Adad1 adenosine deaminase domain containing 1 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220519 MGI 1552126 Adad1 adenosine deaminase domain containing 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15649457 1552126 Adad1 adenosine deaminase domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552127 Zfp644 zinc finger protein 644 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210128 MGI 1552127 Zfp644 zinc finger protein 644 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1552127 Zfp644 zinc finger protein 644 gene MP:0001262 decreased body weight IEA N RGD:5509061 20240523 MGI 1552127 Zfp644 zinc finger protein 644 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1552127 Zfp644 zinc finger protein 644 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1552127 Zfp644 zinc finger protein 644 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1552127 Zfp644 zinc finger protein 644 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210128 MGI 1552127 Zfp644 zinc finger protein 644 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1552127 Zfp644 zinc finger protein 644 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1552127 Zfp644 zinc finger protein 644 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 1552128 Atg101 autophagy related 101 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20210325 MGI PMID:33296658 1552128 Atg101 autophagy related 101 gene MP:0003641 small lung IAGP N RGD:5509061 20210325 MGI PMID:33296658 1552128 Atg101 autophagy related 101 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20210325 MGI PMID:33296658 1552128 Atg101 autophagy related 101 gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20210325 MGI PMID:33296658 1552128 Atg101 autophagy related 101 gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20210325 MGI PMID:33296658 1552128 Atg101 autophagy related 101 gene MP:0010889 small alveolar lamellar bodies IAGP N RGD:5509061 20210325 MGI PMID:33296658 1552128 Atg101 autophagy related 101 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20210325 MGI PMID:33296658 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20201022 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20201022 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20201022 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20201022 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0001726 abnormal allantois morphology IEA N RGD:5509061 20201022 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20201022 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20201022 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20201022 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20201022 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20220519 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20210826 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20180222 MGI PMID:16307915 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0020352 abnormal endoplasmic reticulum physiology IAGP N RGD:5509061 20180222 MGI PMID:16307915 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0020936 abnormal susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:28545059 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0020938 decreased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:28545059 1552130 Uggt1 UDP-glucose glycoprotein glucosyltransferase 1 gene MP:0031039 decreased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:28545059 1552138 Gm2a GM2 ganglioside activator protein gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20230601 MGI 1552138 Gm2a GM2 ganglioside activator protein gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20141003 MGI PMID:9223328 1552138 Gm2a GM2 ganglioside activator protein gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:9223328 1552138 Gm2a GM2 ganglioside activator protein gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9223328 1552138 Gm2a GM2 ganglioside activator protein gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9223328 1552138 Gm2a GM2 ganglioside activator protein gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:9223328 1552138 Gm2a GM2 ganglioside activator protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9223328 1552138 Gm2a GM2 ganglioside activator protein gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9223328 1552138 Gm2a GM2 ganglioside activator protein gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:9223328 1552138 Gm2a GM2 ganglioside activator protein gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9223328 1552138 Gm2a GM2 ganglioside activator protein gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9223328 1552138 Gm2a GM2 ganglioside activator protein gene MP:0004166 abnormal limbic system morphology IAGP N RGD:5509061 20141003 MGI PMID:9223328 1552138 Gm2a GM2 ganglioside activator protein gene MP:0005267 abnormal olfactory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9223328 1552138 Gm2a GM2 ganglioside activator protein gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20230601 MGI 1552138 Gm2a GM2 ganglioside activator protein gene MP:0006300 abnormal entorhinal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9223328 1552138 Gm2a GM2 ganglioside activator protein gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9223328 1552139 Vdac2 voltage-dependent anion channel 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20151112 MGI PMID:19706873 1552139 Vdac2 voltage-dependent anion channel 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20151112 MGI PMID:19706873 1552139 Vdac2 voltage-dependent anion channel 2 gene MP:0009258 abnormal thymocyte apoptosis IAGP N RGD:5509061 20151112 MGI PMID:19706873 1552140 Ece1 endothelin converting enzyme 1 gene MP:0000040 absent middle ear ossicles IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:10811845 1552140 Ece1 endothelin converting enzyme 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:9649553 1552140 Ece1 endothelin converting enzyme 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:10811845 1552140 Ece1 endothelin converting enzyme 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:9649553 1552140 Ece1 endothelin converting enzyme 1 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:10811845 1552140 Ece1 endothelin converting enzyme 1 gene MP:0000299 failure of atrioventricular cushion closure IAGP N RGD:5509061 20141003 MGI PMID:10811845 1552140 Ece1 endothelin converting enzyme 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10811845 1552140 Ece1 endothelin converting enzyme 1 gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:10811845 1552140 Ece1 endothelin converting enzyme 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10811845 1552140 Ece1 endothelin converting enzyme 1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:10811845 1552140 Ece1 endothelin converting enzyme 1 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9649553 1552140 Ece1 endothelin converting enzyme 1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:10811845 1552140 Ece1 endothelin converting enzyme 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:9649553 1552140 Ece1 endothelin converting enzyme 1 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:10811845 1552140 Ece1 endothelin converting enzyme 1 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0003494 parathyroid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0003499 thyroid gland hypoplasia IAGP N RGD:5509061 20150326 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0003798 abnormal Harderian gland pigmentation IAGP N RGD:5509061 20150326 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0004159 double aortic arch IAGP N RGD:5509061 20141003 MGI PMID:9649553 1552140 Ece1 endothelin converting enzyme 1 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0004318 absent incus IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0004319 absent malleus IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0004460 alisphenoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0004475 palatine bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20170921 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10811845 1552140 Ece1 endothelin converting enzyme 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9649553 1552140 Ece1 endothelin converting enzyme 1 gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9649553 1552140 Ece1 endothelin converting enzyme 1 gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9649553 1552140 Ece1 endothelin converting enzyme 1 gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20150326 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0009525 abnormal submandibular duct morphology IAGP N RGD:5509061 20150326 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0009707 absent external auditory canal IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:9649553 1552140 Ece1 endothelin converting enzyme 1 gene MP:0009905 absent tongue IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0010191 abnormal choroid melanocyte morphology IAGP N RGD:5509061 20150326 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:10811845 1552140 Ece1 endothelin converting enzyme 1 gene MP:0010426 abnormal heart and great artery attachment IAGP N RGD:5509061 20141003 MGI PMID:10811845 1552140 Ece1 endothelin converting enzyme 1 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:9649553 1552140 Ece1 endothelin converting enzyme 1 gene MP:0010486 absent right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0010572 persistent right dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:9649553 1552140 Ece1 endothelin converting enzyme 1 gene MP:0010720 absent sublingual duct IAGP N RGD:5509061 20150326 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0010722 persistent cervical thymus IAGP N RGD:5509061 20150326 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10811845 1552140 Ece1 endothelin converting enzyme 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0012310 persistent ductus caroticus IAGP N RGD:5509061 20141003 MGI PMID:9649553 1552140 Ece1 endothelin converting enzyme 1 gene MP:0013917 persistent right 6th pharyngeal arch artery IAGP N RGD:5509061 20191219 MGI PMID:9649553 1552140 Ece1 endothelin converting enzyme 1 gene MP:0030122 temporal bone squamous part hypoplasia IAGP N RGD:5509061 20171005 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20191128 MGI PMID:9449665 1552140 Ece1 endothelin converting enzyme 1 gene MP:0031550 abnormal atrioventricular valve development IAGP N RGD:5509061 20240104 MGI PMID:10811845 1552142 Mon1b MON1 homolog B, secretory traffciking associated gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1552142 Mon1b MON1 homolog B, secretory traffciking associated gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1552142 Mon1b MON1 homolog B, secretory traffciking associated gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1552144 Actl6a actin-like 6A gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20230601 MGI 1552144 Actl6a actin-like 6A gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1552144 Actl6a actin-like 6A gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0002872 polycythemia IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1552144 Actl6a actin-like 6A gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1552144 Actl6a actin-like 6A gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552144 Actl6a actin-like 6A gene MP:0011903 decreased hematopoietic stem cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:23018638 1552145 Dnajc17 DnaJ heat shock protein family (Hsp40) member C17 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200310 MGI 1552145 Dnajc17 DnaJ heat shock protein family (Hsp40) member C17 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1552145 Dnajc17 DnaJ heat shock protein family (Hsp40) member C17 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20221215 MGI 1552145 Dnajc17 DnaJ heat shock protein family (Hsp40) member C17 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20160132 1552145 Dnajc17 DnaJ heat shock protein family (Hsp40) member C17 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552150 Arhgap29 Rho GTPase activating protein 29 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1552150 Arhgap29 Rho GTPase activating protein 29 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230601 MGI 1552150 Arhgap29 Rho GTPase activating protein 29 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1552150 Arhgap29 Rho GTPase activating protein 29 gene MP:0009884 palatal shelf fusion with tongue or mandible IAGP N RGD:5509061 20200310 MGI PMID:28817352 1552150 Arhgap29 Rho GTPase activating protein 29 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20200310 MGI PMID:28817352 1552150 Arhgap29 Rho GTPase activating protein 29 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28817352 1552150 Arhgap29 Rho GTPase activating protein 29 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552150 Arhgap29 Rho GTPase activating protein 29 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1552150 Arhgap29 Rho GTPase activating protein 29 gene MP:0013530 abnormal periderm morphology IAGP N RGD:5509061 20200310 MGI PMID:28817352 1552150 Arhgap29 Rho GTPase activating protein 29 gene MP:0030179 abnormal oral epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:28817352 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:1606615 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17893328 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15380515 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17893328 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23576758 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:17893328 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:1606615 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:1606615 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17893328 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:8898232 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12702876 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11290321 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12702876 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15380515 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:15380515 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11940649 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15380515 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:1606615 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16940357 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:8898232 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12397175 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8608936 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11940649 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23576758 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11940649 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0003121 genetic imprinting IAGP N RGD:5509061 20141003 MGI PMID:9679064 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:15890782 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20230727 MGI PMID:34516921 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20230727 MGI PMID:34516921 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:11290321 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:18221528 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:9679064 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:21383065 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17893328 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:15380515 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:8898232 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:11888894 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16940357 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20230727 MGI PMID:34516921 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20230727 MGI PMID:34516921 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:1606615 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:17182866 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21383065 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:8898232 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20230727 MGI PMID:34516921 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:8898232 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230727 MGI PMID:34516921 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1606615 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8898232 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21383065 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15890782 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15890782 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0012131 small visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:1606615 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0012207 decreased neuronal stem cell self-renewal IAGP N RGD:5509061 20230727 MGI PMID:34516921 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20230727 MGI PMID:34516921 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11940649 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:1606615 1552151 Dnmt1 DNA methyltransferase 1 gene MP:0014257 embryonic lethality prior to tooth bud stage, complete penetrance IAGP N RGD:5509061 20230727 MGI PMID:34516921 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20240523 MGI 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20210401 MGI PMID:23902639 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20210401 MGI PMID:23902639 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:20093357 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20210401 MGI PMID:23902639 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20210401 MGI PMID:23902639 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20240523 MGI 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0002965 increased circulating serum albumin level IAGP N RGD:5509061 20210401 MGI PMID:23902639 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20210401 MGI PMID:23902639 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20093357 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0005331 insulin resistance IAGP N RGD:5509061 20210401 MGI PMID:23902639 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20210401 MGI PMID:23902639 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20093357 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20210401 MGI PMID:23902639 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:20093357 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20093357 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0010127 hypervolemia IAGP N RGD:5509061 20141003 MGI PMID:20093357 1552153 Agtrap angiotensin II, type I receptor-associated protein gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20240523 MGI 1552156 Pon3 paraoxonase 3 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0000611 jaundice IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0002830 gallstones IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22441669 1552156 Pon3 paraoxonase 3 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:21952037 1552156 Pon3 paraoxonase 3 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0009121 increased white fat cell lipid droplet size IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:21952037 1552156 Pon3 paraoxonase 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21952037 1552156 Pon3 paraoxonase 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21952037 1552156 Pon3 paraoxonase 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21952037 1552156 Pon3 paraoxonase 3 gene MP:0012338 decreased bile salt level IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552156 Pon3 paraoxonase 3 gene MP:0012604 decreased glutathione level IAGP N RGD:5509061 20141003 MGI PMID:22441669 1552156 Pon3 paraoxonase 3 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20170406 MGI PMID:25477283 1552157 Rnf135 ring finger protein 135 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210826 MGI 1552157 Rnf135 ring finger protein 135 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20181227 MGI 1552157 Rnf135 ring finger protein 135 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1552157 Rnf135 ring finger protein 135 gene MP:0001127 small ovary IEA N RGD:5509061 20210826 MGI 1552157 Rnf135 ring finger protein 135 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1552157 Rnf135 ring finger protein 135 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1552157 Rnf135 ring finger protein 135 gene MP:0002637 small uterus IEA N RGD:5509061 20210826 MGI 1552157 Rnf135 ring finger protein 135 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:19323995 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:8637595 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:11807038 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20141003 MGI PMID:19109949 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11807038 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:15797020 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:18321480 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11807038 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15647317 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15797020 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19109949 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:18434421 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11807038 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:19109949 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19459208 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150430 MGI PMID:24608965 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:19109949 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:21765429 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18321480 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8632990 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0004165 abnormal lateral geniculate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19323995 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0004267 abnormal optic tract morphology IAGP N RGD:5509061 20141003 MGI PMID:19323995 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11807038 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:14559155 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141225 MGI PMID:24736625 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18321480 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15797020 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18321480 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18321480 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0006156 abnormal visual pursuit IAGP N RGD:5509061 20141003 MGI PMID:19323995 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20141003 MGI PMID:19109949 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18434421 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8632990 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:21765429 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20230713 MGI PMID:19323995 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11807038 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:11807038 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:18321480 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:19323995 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:21765429 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:8632990 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11807038 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18321480 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19323995 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15647317 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18434421 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:8637595 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008105 increased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:11807038 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:18321480 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008259 abnormal optic disk morphology IAGP N RGD:5509061 20141003 MGI PMID:15797020 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:11807038 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:15797020 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:18321480 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:19109949 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:8632990 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:18321480 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:8632990 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:18321480 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:8632990 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0008847 abnormal suprachiasmatic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:21765429 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0009639 abnormal olivary pretectal nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:21765429 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:15797020 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0020468 abnormal circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:21765429 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:19323995 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:19323995 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:15647317 1552160 Pou4f2 POU domain, class 4, transcription factor 2 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:18321480 1552164 Ahdc1 AT hook, DNA binding motif, containing 1 gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20240307 MGI PMID:35585237 1552164 Ahdc1 AT hook, DNA binding motif, containing 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20240307 MGI PMID:35585237 1552164 Ahdc1 AT hook, DNA binding motif, containing 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20240307 MGI PMID:35585237 1552164 Ahdc1 AT hook, DNA binding motif, containing 1 gene MP:0000445 short snout IAGP N RGD:5509061 20240307 MGI PMID:35585237 1552164 Ahdc1 AT hook, DNA binding motif, containing 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20240307 MGI PMID:35585237 1552164 Ahdc1 AT hook, DNA binding motif, containing 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20240307 MGI PMID:35585237 1552164 Ahdc1 AT hook, DNA binding motif, containing 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20240307 MGI PMID:35585237 1552164 Ahdc1 AT hook, DNA binding motif, containing 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20240307 MGI PMID:35585237 1552164 Ahdc1 AT hook, DNA binding motif, containing 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20240307 MGI PMID:35585237 1552164 Ahdc1 AT hook, DNA binding motif, containing 1 gene MP:0009827 skin detachment IAGP N RGD:5509061 20240307 MGI PMID:35585237 1552164 Ahdc1 AT hook, DNA binding motif, containing 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20240307 MGI PMID:35585237 1552164 Ahdc1 AT hook, DNA binding motif, containing 1 gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20240307 MGI PMID:35585237 1552165 Slc10a6 solute carrier family 10 (sodium/bile acid cotransporter family), member 6 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20210401 MGI PMID:28743544 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23064362 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23064362 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0001194 dermatitis IAGP N RGD:5509061 20181122 MGI PMID:25902485 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:14978083 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0001830 decreased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:17351619 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17351619 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16688182 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14978083 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16688182 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:17351619 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23034650 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16688182 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16688182 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:15657292 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:17277169 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14978083 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23064362 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17277169 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14978083 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15657292 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14978083 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17351619 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23064362 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:14978083 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:16920909 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20151112 MGI PMID:22089030 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17277169 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20151112 MGI PMID:22089030 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20151112 MGI PMID:22089030 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:15657292 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:17277169 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:23064362 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:16688182 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23064362 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20151112 MGI PMID:22089030 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16920909 1552166 Il23a interleukin 23, alpha subunit p19 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18264109 1552167 Phkb phosphorylase kinase beta gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20221124 MGI PMID:36077341 1552167 Phkb phosphorylase kinase beta gene MP:0000599 enlarged liver IAGP N RGD:5509061 20221124 MGI PMID:36077341 1552167 Phkb phosphorylase kinase beta gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201022 MGI 1552167 Phkb phosphorylase kinase beta gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1552167 Phkb phosphorylase kinase beta gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20221124 MGI PMID:36077341 1552167 Phkb phosphorylase kinase beta gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20221124 MGI PMID:36077341 1552167 Phkb phosphorylase kinase beta gene MP:0002715 decreased glycogen catabolism rate IAGP N RGD:5509061 20221124 MGI PMID:36077341 1552167 Phkb phosphorylase kinase beta gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1552167 Phkb phosphorylase kinase beta gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1552167 Phkb phosphorylase kinase beta gene MP:0002981 increased liver weight IAGP N RGD:5509061 20221124 MGI PMID:36077341 1552167 Phkb phosphorylase kinase beta gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1552167 Phkb phosphorylase kinase beta gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1552167 Phkb phosphorylase kinase beta gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20221124 MGI PMID:36077341 1552167 Phkb phosphorylase kinase beta gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20221124 MGI PMID:36077341 1552167 Phkb phosphorylase kinase beta gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20221124 MGI PMID:36077341 1552167 Phkb phosphorylase kinase beta gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20221124 MGI PMID:36077341 1552167 Phkb phosphorylase kinase beta gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1552167 Phkb phosphorylase kinase beta gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20221124 MGI PMID:36077341 1552167 Phkb phosphorylase kinase beta gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552167 Phkb phosphorylase kinase beta gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20221124 MGI PMID:36077341 1552167 Phkb phosphorylase kinase beta gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20221124 MGI PMID:36077341 1552167 Phkb phosphorylase kinase beta gene MP:0030974 enhanced gluconeogenesis IAGP N RGD:5509061 20221124 MGI PMID:36077341 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0000745 tremors IAGP N RGD:5509061 20210617 MGI PMID:30876848 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0000745 tremors IAGP N RGD:5509061 20241017 MGI PMID:35760530 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20151224 MGI PMID:24507192 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20210617 MGI PMID:30876848 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:11955447 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:16407399 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11955448 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20151203 MGI PMID:24423059 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20180607 MGI PMID:28041882 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:11955447 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20161027 MGI PMID:27008863 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20210617 MGI PMID:30876848 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20161027 MGI PMID:27008863 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20161027 MGI PMID:27008863 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20161027 MGI PMID:27008863 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20161027 MGI PMID:27008863 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20161027 MGI PMID:27008863 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0002064 seizures IAGP N RGD:5509061 20210617 MGI PMID:30876848 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0003647 absent oligodendrocytes IAGP N RGD:5509061 20141003 MGI PMID:11955447 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0003647 absent oligodendrocytes IAGP N RGD:5509061 20141003 MGI PMID:16407399 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:11955447 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20151224 MGI PMID:24507192 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:11955447 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20210617 MGI PMID:30876848 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20241017 MGI PMID:35760530 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0005473 decreased triiodothyronine level IAGP N RGD:5509061 20241017 MGI PMID:35760530 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20161027 MGI PMID:27008863 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20151224 MGI PMID:24507192 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20210617 MGI PMID:30876848 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20230713 MGI PMID:26928066 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20241017 MGI PMID:35760530 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0009941 abnormal olfactory bulb interneuron morphology IAGP N RGD:5509061 20151224 MGI PMID:24507192 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20151224 MGI PMID:24507192 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20151224 MGI PMID:24507192 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210617 MGI PMID:30876848 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20151224 MGI PMID:24507192 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11955447 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16407399 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20161027 MGI PMID:27008863 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20230713 MGI PMID:26928066 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20241017 MGI PMID:35760530 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20161027 MGI PMID:27008863 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20180607 MGI PMID:28041882 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20210617 MGI PMID:30876848 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20230713 MGI PMID:26928066 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0014318 abnormal oligodendrocyte differentiation IAGP N RGD:5509061 20241017 MGI PMID:35760530 1552169 Olig1 oligodendrocyte transcription factor 1 gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:11955447 1552170 Incenp inner centromere protein gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10369859 1552170 Incenp inner centromere protein gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10369859 1552170 Incenp inner centromere protein gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:10369859 1552170 Incenp inner centromere protein gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:10369859 1552170 Incenp inner centromere protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10369859 1552172 Rlf rearranged L-myc fusion sequence gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:19099580 1552172 Rlf rearranged L-myc fusion sequence gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:19099580 1552173 Acat2 acetyl-Coenzyme A acetyltransferase 2 gene MP:0001257 increased body length IEA N RGD:5509061 20210128 MGI 1552173 Acat2 acetyl-Coenzyme A acetyltransferase 2 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1552173 Acat2 acetyl-Coenzyme A acetyltransferase 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20161201 MGI 1552173 Acat2 acetyl-Coenzyme A acetyltransferase 2 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20210128 MGI 1552173 Acat2 acetyl-Coenzyme A acetyltransferase 2 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20161201 MGI 1552173 Acat2 acetyl-Coenzyme A acetyltransferase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16754665 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0000505 decreased digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:16754665 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0001577 anemia IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0003285 gastric hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21084694 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:16754665 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:21084694 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16754665 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0004731 increased circulating gastrin level IAGP N RGD:5509061 20141003 MGI PMID:16754665 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0008001 hypochlorhydria IAGP N RGD:5509061 20141003 MGI PMID:16754665 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0008003 achlorhydria IAGP N RGD:5509061 20141003 MGI PMID:16754665 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0008003 achlorhydria IAGP N RGD:5509061 20141003 MGI PMID:21084694 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20141003 MGI PMID:16754665 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20141003 MGI PMID:21084694 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0010092 increased circulating magnesium level IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0011891 decreased circulating ferritin level IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0013569 gastric gland hyperplasia IAGP N RGD:5509061 20150312 MGI PMID:16754665 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0013569 gastric gland hyperplasia IAGP N RGD:5509061 20161027 MGI PMID:25127743 1552174 Kcne2 potassium voltage-gated channel, Isk-related subfamily, gene 2 gene MP:0013578 abnormal stomach glandular region morphology IAGP N RGD:5509061 20150312 MGI PMID:16754665 1552177 Ube2q1 ubiquitin-conjugating enzyme E2Q family member 1 gene MP:0001377 abnormal mating frequency IAGP N RGD:5509061 20200310 MGI PMID:23108111 1552177 Ube2q1 ubiquitin-conjugating enzyme E2Q family member 1 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20200310 MGI PMID:23108111 1552177 Ube2q1 ubiquitin-conjugating enzyme E2Q family member 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:23108111 1552177 Ube2q1 ubiquitin-conjugating enzyme E2Q family member 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20200310 MGI PMID:23108111 1552177 Ube2q1 ubiquitin-conjugating enzyme E2Q family member 1 gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20200310 MGI PMID:23108111 1552177 Ube2q1 ubiquitin-conjugating enzyme E2Q family member 1 gene MP:0008976 delayed female fertility IAGP N RGD:5509061 20200310 MGI PMID:23108111 1552177 Ube2q1 ubiquitin-conjugating enzyme E2Q family member 1 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20200310 MGI PMID:23108111 1552177 Ube2q1 ubiquitin-conjugating enzyme E2Q family member 1 gene MP:0011103 embryonic lethality at implantation, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23108111 1552179 Mtr 5-methyltetrahydrofolate-homocysteine methyltransferase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11158293 1552179 Mtr 5-methyltetrahydrofolate-homocysteine methyltransferase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20180920 MGI PMID:11158293 1552179 Mtr 5-methyltetrahydrofolate-homocysteine methyltransferase gene MP:0030644 increased circulating methionine level IAGP N RGD:5509061 20180920 MGI PMID:11158293 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:14701741 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:14701741 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:14701741 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:15256493 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:14701741 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:14701741 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:14701741 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:15256493 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20141003 MGI PMID:14701741 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20141003 MGI PMID:15256493 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:14701741 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:14701741 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0005149 abnormal gubernaculum morphology IAGP N RGD:5509061 20141003 MGI PMID:15256493 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:14701741 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15256493 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0009722 abnormal nipple development IAGP N RGD:5509061 20150402 MGI PMID:15256493 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0011727 ectopic ovary IAGP N RGD:5509061 20141003 MGI PMID:15256493 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0013713 decreased nipple size IAGP N RGD:5509061 20150402 MGI PMID:14701741 1552181 Rxfp1 relaxin/insulin-like family peptide receptor 1 gene MP:0013713 decreased nipple size IAGP N RGD:5509061 20150402 MGI PMID:15256493 1552182 Pla2g3 phospholipase A2, group III gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20200310 MGI PMID:23624557 1552182 Pla2g3 phospholipase A2, group III gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:23624557 1552182 Pla2g3 phospholipase A2, group III gene MP:0001849 ear inflammation IAGP N RGD:5509061 20200310 MGI PMID:23624557 1552182 Pla2g3 phospholipase A2, group III gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0002686 globozoospermia IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0005462 abnormal mast cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:23624557 1552182 Pla2g3 phospholipase A2, group III gene MP:0005535 abnormal body temperature IAGP N RGD:5509061 20200310 MGI PMID:23624557 1552182 Pla2g3 phospholipase A2, group III gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20200310 MGI PMID:23624557 1552182 Pla2g3 phospholipase A2, group III gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20200310 MGI PMID:23624557 1552182 Pla2g3 phospholipase A2, group III gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0009280 decreased activated sperm motility IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0014467 increased sperm mitochondrial size IAGP N RGD:5509061 20240613 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0014468 disorganized sperm mitochondrial sheath IAGP N RGD:5509061 20240613 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20200310 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20220630 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220630 MGI PMID:20424323 1552182 Pla2g3 phospholipase A2, group III gene MP:0031410 biflagellated sperm IAGP N RGD:5509061 20220630 MGI PMID:20424323 1552183 Lemd2 LEM domain containing 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200310 MGI 1552183 Lemd2 LEM domain containing 2 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0002083 premature death IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1552183 Lemd2 LEM domain containing 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552183 Lemd2 LEM domain containing 2 gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20230330 MGI PMID:36377660 1552183 Lemd2 LEM domain containing 2 gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20231207 MGI 1552183 Lemd2 LEM domain containing 2 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0012706 decreased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1552183 Lemd2 LEM domain containing 2 gene MP:0013906 absent embryonic telencephalon IAGP N RGD:5509061 20200310 MGI PMID:25790465 1552183 Lemd2 LEM domain containing 2 gene MP:0031328 delayed skeletal muscle regeneration IAGP N RGD:5509061 20220106 MGI PMID:25790465 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20211209 MGI PMID:31798959 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20211209 MGI PMID:31798959 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20211209 MGI PMID:31798959 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20211209 MGI PMID:31798959 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20211209 MGI PMID:31798959 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20211209 MGI PMID:31798959 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20211209 MGI PMID:31798959 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0020103 decreased hepatic glucose production IAGP N RGD:5509061 20191010 MGI PMID:31230984 1552184 Or4m1 olfactory receptor family 4 subfamily M member 1 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20211209 MGI PMID:31798959 1552186 Lyzl6 lysozyme-like 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:27357688 1552188 Galc galactosylceramidase gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20441793 1552188 Galc galactosylceramidase gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:20441793 1552188 Galc galactosylceramidase gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:20441793 1552188 Galc galactosylceramidase gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16624958 1552188 Galc galactosylceramidase gene MP:0000160 kyphosis IAGP N RGD:5509061 20210805 MGI PMID:34142127 1552188 Galc galactosylceramidase gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:6319815 1552188 Galc galactosylceramidase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:10861297 1552188 Galc galactosylceramidase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:10861297 1552188 Galc galactosylceramidase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10861297 1552188 Galc galactosylceramidase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10415153 1552188 Galc galactosylceramidase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11461188 1552188 Galc galactosylceramidase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12270695 1552188 Galc galactosylceramidase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16624958 1552188 Galc galactosylceramidase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23620143 1552188 Galc galactosylceramidase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:7417782 1552188 Galc galactosylceramidase gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:23620143 1552188 Galc galactosylceramidase gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:7417782 1552188 Galc galactosylceramidase gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:11461188 1552188 Galc galactosylceramidase gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:23620143 1552188 Galc galactosylceramidase gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:12270695 1552188 Galc galactosylceramidase gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20141003 MGI PMID:12270695 1552188 Galc galactosylceramidase gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:12270695 1552188 Galc galactosylceramidase gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:10415153 1552188 Galc galactosylceramidase gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:10861297 1552188 Galc galactosylceramidase gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:11371512 1552188 Galc galactosylceramidase gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:11461188 1552188 Galc galactosylceramidase gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:12270695 1552188 Galc galactosylceramidase gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:16624958 1552188 Galc galactosylceramidase gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:23620143 1552188 Galc galactosylceramidase gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10374755 1552188 Galc galactosylceramidase gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:23620143 1552188 Galc galactosylceramidase gene MP:0000958 peripheral nervous system degeneration IEA N RGD:5509061 20111116 MGI 1552188 Galc galactosylceramidase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20441793 1552188 Galc galactosylceramidase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23620143 1552188 Galc galactosylceramidase gene MP:0001265 decreased body size IAGP N RGD:5509061 20210805 MGI PMID:34142127 1552188 Galc galactosylceramidase gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16624958 1552188 Galc galactosylceramidase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12270695 1552188 Galc galactosylceramidase gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:16624958 1552188 Galc galactosylceramidase gene MP:0001524 impaired limb coordination IEA N RGD:5509061 20111116 MGI 1552188 Galc galactosylceramidase gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:20441793 1552188 Galc galactosylceramidase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:10861297 1552188 Galc galactosylceramidase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:11371512 1552188 Galc galactosylceramidase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:20441793 1552188 Galc galactosylceramidase gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:6306338 1552188 Galc galactosylceramidase gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:11461188 1552188 Galc galactosylceramidase gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10861297 1552188 Galc galactosylceramidase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10415153 1552188 Galc galactosylceramidase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10861297 1552188 Galc galactosylceramidase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11461188 1552188 Galc galactosylceramidase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12270695 1552188 Galc galactosylceramidase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16624958 1552188 Galc galactosylceramidase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23620143 1552188 Galc galactosylceramidase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7417782 1552188 Galc galactosylceramidase gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:20441793 1552188 Galc galactosylceramidase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:6319815 1552188 Galc galactosylceramidase gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:6693925 1552188 Galc galactosylceramidase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12270695 1552188 Galc galactosylceramidase gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12270695 1552188 Galc galactosylceramidase gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16624958 1552188 Galc galactosylceramidase gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:10415153 1552188 Galc galactosylceramidase gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:23620143 1552188 Galc galactosylceramidase gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:10861297 1552188 Galc galactosylceramidase gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:7417782 1552188 Galc galactosylceramidase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10861297 1552188 Galc galactosylceramidase gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12270695 1552188 Galc galactosylceramidase gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:10861297 1552188 Galc galactosylceramidase gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:20441793 1552188 Galc galactosylceramidase gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23620143 1552188 Galc galactosylceramidase gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:6306338 1552188 Galc galactosylceramidase gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:7417782 1552188 Galc galactosylceramidase gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:20441793 1552188 Galc galactosylceramidase gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20210805 MGI PMID:34142127 1552188 Galc galactosylceramidase gene MP:0004875 increased mean systemic arterial blood pressure IEA N RGD:5509061 20190103 MGI 1552188 Galc galactosylceramidase gene MP:0004967 abnormal kidney epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:6319815 1552188 Galc galactosylceramidase gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:11461188 1552188 Galc galactosylceramidase gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:7417782 1552188 Galc galactosylceramidase gene MP:0005167 abnormal blood-brain barrier function IAGP N RGD:5509061 20141003 MGI PMID:10415153 1552188 Galc galactosylceramidase gene MP:0005333 decreased heart rate IEA N RGD:5509061 20190103 MGI 1552188 Galc galactosylceramidase gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:23620143 1552188 Galc galactosylceramidase gene MP:0005405 axon degeneration IEA N RGD:5509061 20111116 MGI 1552188 Galc galactosylceramidase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11461188 1552188 Galc galactosylceramidase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16624958 1552188 Galc galactosylceramidase gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16624958 1552188 Galc galactosylceramidase gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:11371512 1552188 Galc galactosylceramidase gene MP:0006143 increased systemic arterial diastolic blood pressure IEA N RGD:5509061 20190103 MGI 1552188 Galc galactosylceramidase gene MP:0008026 abnormal brain white matter morphology IEA N RGD:5509061 20111116 MGI 1552188 Galc galactosylceramidase gene MP:0008027 abnormal spinal cord white matter morphology IEA N RGD:5509061 20111116 MGI 1552188 Galc galactosylceramidase gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23620143 1552188 Galc galactosylceramidase gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20141003 MGI PMID:6693925 1552188 Galc galactosylceramidase gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:23620143 1552188 Galc galactosylceramidase gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:10415153 1552188 Galc galactosylceramidase gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10861297 1552188 Galc galactosylceramidase gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0009046 muscle twitch IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:12270695 1552188 Galc galactosylceramidase gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10861297 1552188 Galc galactosylceramidase gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:10374755 1552188 Galc galactosylceramidase gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20141003 MGI PMID:20441793 1552188 Galc galactosylceramidase gene MP:0009978 abnormal cerebellum white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:10415153 1552188 Galc galactosylceramidase gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20141003 MGI PMID:12270695 1552188 Galc galactosylceramidase gene MP:0010170 abnormal glial cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10374755 1552188 Galc galactosylceramidase gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:20441793 1552188 Galc galactosylceramidase gene MP:0010892 increased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:21389217 1552188 Galc galactosylceramidase gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1552188 Galc galactosylceramidase gene MP:0030825 decreased femur size IAGP N RGD:5509061 20181018 MGI PMID:20441793 1552188 Galc galactosylceramidase gene MP:0030826 decreased femur weight IAGP N RGD:5509061 20181018 MGI PMID:20441793 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000100 abnormal ethmoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11776395 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:16598713 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20170713 MGI PMID:28176446 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:9126927 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:9126927 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:9126927 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:11776395 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16598713 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16598713 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16598713 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:16598713 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16598713 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16598713 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16598713 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001785 edema IAGP N RGD:5509061 20170713 MGI PMID:28176446 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9126927 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20170713 MGI PMID:28176446 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20170713 MGI PMID:28176446 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18467597 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002068 abnormal parental behavior IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18467597 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9126927 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16598713 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:28176446 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20170713 MGI PMID:28176446 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:11776395 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20141003 MGI PMID:11776395 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002244 abnormal turbinate morphology IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002244 abnormal turbinate morphology IAGP N RGD:5509061 20141003 MGI PMID:11776395 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002729 abnormal inner ear canal morphology IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0002980 abnormal postural reflex IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20170713 MGI PMID:28176446 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0003143 enlarged otoliths IAGP N RGD:5509061 20151001 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0003144 decreased otolith number IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0003164 decreased posterior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0003169 abnormal scala media morphology IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:9126927 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004105 cornea abrasion IAGP N RGD:5509061 20141003 MGI PMID:18436818 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:16598713 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20170713 MGI PMID:28176446 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:18436818 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004340 short scapula IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004409 abnormal crista ampullaris neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004477 turbinate hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20171207 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004642 fused metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004681 intervertebral disk hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:16824956 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9126927 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9126927 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9126927 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005163 cyclopia IAGP N RGD:5509061 20170713 MGI PMID:28176446 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11776395 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:18436818 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18436818 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:18467597 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:16824956 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16598713 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11776395 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:16598713 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0008052 abnormal serous gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9126927 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9126927 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0008170 decreased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0008194 abnormal memory B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11776395 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:9126927 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0009727 abnormal navicular morphology IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:11776395 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0009892 palate bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0009946 abnormal olfactory bulb layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11776395 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11776395 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0009951 abnormal olfactory bulb mitral cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11776395 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9126927 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18436818 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20170713 MGI PMID:28176446 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16598713 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141003 MGI PMID:18436818 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:16598713 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20230810 MGI PMID:18436818 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20240627 MGI PMID:11776395 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0013945 abnormal elbow joint morphology IAGP N RGD:5509061 20181025 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0014012 abnormal cranial blood vasculature morphology IAGP N RGD:5509061 20170713 MGI PMID:28176446 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20150702 MGI 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0020858 cornea epithelium hypoplasia IAGP N RGD:5509061 20181101 MGI PMID:18436818 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0021208 median cleft palate IAGP N RGD:5509061 20221201 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0021210 bilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0021211 unilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0030259 mandibular condyloid process hypoplasia IAGP N RGD:5509061 20171207 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0030285 mandibular coronoid process hypoplasia IAGP N RGD:5509061 20171207 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0030304 abnormal cribriform plate morphology IAGP N RGD:5509061 20171109 MGI PMID:11776395 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0030373 Meckel's cartilage hyperplasia IAGP N RGD:5509061 20171207 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0030829 abnormal hip joint morphology IAGP N RGD:5509061 20181025 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0030860 patellar dislocation IAGP N RGD:5509061 20181025 MGI PMID:9389660 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:21980308 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0031447 unilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0031447 unilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:11776395 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0031447 unilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:13539273 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:10669096 1552190 Zeb1 zinc finger E-box binding homeobox 1 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:10669096 1552191 Wif1 Wnt inhibitory factor 1 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:19307728 1552191 Wif1 Wnt inhibitory factor 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19307728 1552191 Wif1 Wnt inhibitory factor 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19307728 1552191 Wif1 Wnt inhibitory factor 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19307728 1552198 Ms4a2 membrane-spanning 4-domains, subfamily A, member 2 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10069418 1552198 Ms4a2 membrane-spanning 4-domains, subfamily A, member 2 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9586641 1552198 Ms4a2 membrane-spanning 4-domains, subfamily A, member 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:9586641 1552198 Ms4a2 membrane-spanning 4-domains, subfamily A, member 2 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10069418 1552198 Ms4a2 membrane-spanning 4-domains, subfamily A, member 2 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:9586641 1552199 Entpd6 ectonucleoside triphosphate diphosphohydrolase 6 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20201022 MGI 1552199 Entpd6 ectonucleoside triphosphate diphosphohydrolase 6 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1552199 Entpd6 ectonucleoside triphosphate diphosphohydrolase 6 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20150430 MGI 1552199 Entpd6 ectonucleoside triphosphate diphosphohydrolase 6 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1552199 Entpd6 ectonucleoside triphosphate diphosphohydrolase 6 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20093629 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20093629 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:20093629 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20190228 MGI PMID:29306897 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20190228 MGI PMID:29306897 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:20093629 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20190228 MGI PMID:29306897 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0004011 decreased diastolic filling velocity IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0004117 abnormal atrioventricular bundle morphology IAGP N RGD:5509061 20190228 MGI PMID:29306897 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0004124 abnormal Purkinje fiber morphology IAGP N RGD:5509061 20190228 MGI PMID:29306897 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:20093629 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20190228 MGI PMID:29306897 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20190228 MGI PMID:29306897 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0010640 ventricular myocardium compact layer hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20360251 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0012624 decreased acetylcholinesterase activity IAGP N RGD:5509061 20190228 MGI PMID:29306897 1552200 Xirp2 xin actin-binding repeat containing 2 gene MP:0020345 abnormal myocardial fiber currents IAGP N RGD:5509061 20190228 MGI PMID:29306897 1552201 Neurog3 neurogenin 3 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10677506 1552201 Neurog3 neurogenin 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:10677506 1552201 Neurog3 neurogenin 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19487660 1552201 Neurog3 neurogenin 3 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19487660 1552201 Neurog3 neurogenin 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:10677506 1552201 Neurog3 neurogenin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15297605 1552201 Neurog3 neurogenin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:12080087 1552201 Neurog3 neurogenin 3 gene MP:0002791 steatorrhea IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0003016 increased circulating bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19487660 1552201 Neurog3 neurogenin 3 gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0005210 disorganized stomach mucosa IAGP N RGD:5509061 20141003 MGI PMID:12080087 1552201 Neurog3 neurogenin 3 gene MP:0005211 increased stomach mucosa thickness IAGP N RGD:5509061 20141003 MGI PMID:12080087 1552201 Neurog3 neurogenin 3 gene MP:0005214 regional gastric metaplasia IAGP N RGD:5509061 20141003 MGI PMID:12080087 1552201 Neurog3 neurogenin 3 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:18394599 1552201 Neurog3 neurogenin 3 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12080087 1552201 Neurog3 neurogenin 3 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12080087 1552201 Neurog3 neurogenin 3 gene MP:0005218 abnormal pancreatic delta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12080087 1552201 Neurog3 neurogenin 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19487660 1552201 Neurog3 neurogenin 3 gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10677506 1552201 Neurog3 neurogenin 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19487660 1552201 Neurog3 neurogenin 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0008109 abnormal small intestinal microvillus morphology IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0008141 decreased small intestinal microvillus size IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10677506 1552201 Neurog3 neurogenin 3 gene MP:0009161 pancreatic acinar cell zymogen granule accumulation IAGP N RGD:5509061 20141003 MGI PMID:10677506 1552201 Neurog3 neurogenin 3 gene MP:0009165 abnormal endocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:19223466 1552201 Neurog3 neurogenin 3 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0009173 absent pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:10677506 1552201 Neurog3 neurogenin 3 gene MP:0009174 absent pancreatic beta cells IAGP N RGD:5509061 20141003 MGI PMID:10677506 1552201 Neurog3 neurogenin 3 gene MP:0009178 absent pancreatic alpha cells IAGP N RGD:5509061 20141003 MGI PMID:10677506 1552201 Neurog3 neurogenin 3 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0010802 abnormal intestinal enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10677506 1552201 Neurog3 neurogenin 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20364088 1552201 Neurog3 neurogenin 3 gene MP:0011984 decreased enteroendocrine cell number IAGP N RGD:5509061 20210603 MGI PMID:31663849 1552204 Sstr2 somatostatin receptor 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1552204 Sstr2 somatostatin receptor 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1552204 Sstr2 somatostatin receptor 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1552204 Sstr2 somatostatin receptor 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1552204 Sstr2 somatostatin receptor 2 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1552204 Sstr2 somatostatin receptor 2 gene MP:0001200 thick skin IEA N RGD:5509061 20210520 MGI 1552204 Sstr2 somatostatin receptor 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:11029646 1552204 Sstr2 somatostatin receptor 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11029646 1552204 Sstr2 somatostatin receptor 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12752788 1552204 Sstr2 somatostatin receptor 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:11029646 1552204 Sstr2 somatostatin receptor 2 gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:11029646 1552204 Sstr2 somatostatin receptor 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1552204 Sstr2 somatostatin receptor 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20201022 MGI 1552204 Sstr2 somatostatin receptor 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1552204 Sstr2 somatostatin receptor 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:11029646 1552204 Sstr2 somatostatin receptor 2 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:15601946 1552204 Sstr2 somatostatin receptor 2 gene MP:0004494 abnormal synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:12752788 1552204 Sstr2 somatostatin receptor 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:12752788 1552204 Sstr2 somatostatin receptor 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:15548214 1552204 Sstr2 somatostatin receptor 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:12752788 1552204 Sstr2 somatostatin receptor 2 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14750962 1552204 Sstr2 somatostatin receptor 2 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17425570 1552204 Sstr2 somatostatin receptor 2 gene MP:0009084 blind uterus IEA N RGD:5509061 20201022 MGI 1552205 Tmem62 transmembrane protein 62 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240523 MGI 1552205 Tmem62 transmembrane protein 62 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1552206 Tm2d1 TM2 domain containing 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200310 MGI 1552206 Tm2d1 TM2 domain containing 1 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20201231 MGI 1552206 Tm2d1 TM2 domain containing 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20201022 MGI 1552206 Tm2d1 TM2 domain containing 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1552206 Tm2d1 TM2 domain containing 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20200402 MGI 1552206 Tm2d1 TM2 domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552207 Pla2g15 phospholipase A2, group XV gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15781238 1552207 Pla2g15 phospholipase A2, group XV gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16880524 1552207 Pla2g15 phospholipase A2, group XV gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:16880524 1552207 Pla2g15 phospholipase A2, group XV gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16880524 1552207 Pla2g15 phospholipase A2, group XV gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16880524 1552207 Pla2g15 phospholipase A2, group XV gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:16880524 1552207 Pla2g15 phospholipase A2, group XV gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:15781238 1552207 Pla2g15 phospholipase A2, group XV gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:16880524 1552207 Pla2g15 phospholipase A2, group XV gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16880524 1552207 Pla2g15 phospholipase A2, group XV gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16880524 1552207 Pla2g15 phospholipase A2, group XV gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20141003 MGI PMID:16880524 1552207 Pla2g15 phospholipase A2, group XV gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16880524 1552207 Pla2g15 phospholipase A2, group XV gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15781238 1552207 Pla2g15 phospholipase A2, group XV gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15781238 1552207 Pla2g15 phospholipase A2, group XV gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15781238 1552207 Pla2g15 phospholipase A2, group XV gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16880524 1552209 Has1 hyaluronan synthase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20823158 1552209 Has1 hyaluronan synthase 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1552209 Has1 hyaluronan synthase 1 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20210128 MGI 1552210 Osmr oncostatin M receptor gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12855584 1552210 Osmr oncostatin M receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12855584 1552210 Osmr oncostatin M receptor gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12855584 1552210 Osmr oncostatin M receptor gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12855584 1552210 Osmr oncostatin M receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12855584 1552210 Osmr oncostatin M receptor gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12855584 1552210 Osmr oncostatin M receptor gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12855584 1552210 Osmr oncostatin M receptor gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12855584 1552210 Osmr oncostatin M receptor gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12855584 1552210 Osmr oncostatin M receptor gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0011939 increased food intake IAGP N RGD:5509061 20141106 MGI PMID:24695736 1552210 Osmr oncostatin M receptor gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240321 MGI PMID:24695736 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:15778975 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17079272 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:17079272 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17079272 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15778975 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:15778975 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0002163 abnormal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17079272 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17079272 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:15778975 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15778975 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17079272 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17079272 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0004757 abnormal distal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17079272 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0005310 abnormal salivary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:17079272 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:17079272 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:17079272 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17079272 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:17079272 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0011754 abnormal kidney collecting duct intercalated cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17079272 1552211 Tfcp2l1 transcription factor CP2-like 1 gene MP:0013580 abnormal nasal gland morphology IAGP N RGD:5509061 20150305 MGI PMID:17079272 1552216 Ppm1k protein phosphatase 1K (PP2C domain containing) gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:19411760 1552216 Ppm1k protein phosphatase 1K (PP2C domain containing) gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20200310 MGI PMID:19411760 1552216 Ppm1k protein phosphatase 1K (PP2C domain containing) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19411760 1552220 Gtf2h3 general transcription factor IIH, polypeptide 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210826 MGI 1552220 Gtf2h3 general transcription factor IIH, polypeptide 3 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20240523 MGI 1552220 Gtf2h3 general transcription factor IIH, polypeptide 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1552220 Gtf2h3 general transcription factor IIH, polypeptide 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220811 MGI 1552223 Lmo7 LIM domain only 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12761045 1552223 Lmo7 LIM domain only 7 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19215226 1552223 Lmo7 LIM domain only 7 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12761045 1552223 Lmo7 LIM domain only 7 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12761045 1552223 Lmo7 LIM domain only 7 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:12761045 1552223 Lmo7 LIM domain only 7 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:12761045 1552223 Lmo7 LIM domain only 7 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12761045 1552223 Lmo7 LIM domain only 7 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:12761045 1552223 Lmo7 LIM domain only 7 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12761045 1552223 Lmo7 LIM domain only 7 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19215226 1552223 Lmo7 LIM domain only 7 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12761045 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0000111 cleft palate IAGP N RGD:5509061 20221020 MGI PMID:33772547 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:14645126 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:14645126 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:14645126 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0001265 decreased body size IEA N RGD:5509061 20141003 MGI 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:14645126 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:14645126 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:14645126 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17150957 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:14645126 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:14645126 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:14645126 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:14645126 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221020 MGI PMID:33772547 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0010487 abnormal right subclavian artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0010488 abnormal left subclavian artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:33772547 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14645126 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14645126 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23451234 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20221020 MGI PMID:33772547 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0021208 median cleft palate IAGP N RGD:5509061 20221201 MGI PMID:33772547 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:33772547 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0030191 narrow snout IEA N RGD:5509061 20171019 MGI 1552225 Rere arginine glutamic acid dipeptide (RE) repeats gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:33772547 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18378898 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000111 cleft palate IEA N RGD:5509061 20210520 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210520 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210128 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:18378898 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:18378898 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000562 polydactyly IEA N RGD:5509061 20141003 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000564 syndactyly IEA N RGD:5509061 20141003 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:18378898 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000650 mesocardia IEA N RGD:5509061 20141003 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:18378898 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18378898 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160421 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18378898 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:18378898 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20141003 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20160421 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0002367 abnormal thymus lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:18378898 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0003130 anal atresia IEA N RGD:5509061 20141003 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20160811 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:18378898 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20160811 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20160811 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220811 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0004159 double aortic arch IEA N RGD:5509061 20141003 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0004651 increased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0004653 absent caudal vertebrae IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0004656 absent sacral vertebrae IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0004694 absent patella IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0005155 herniated intestine IAGP N RGD:5509061 20141003 MGI PMID:18378898 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20210520 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0005430 absent fibula IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20160811 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:18378898 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:18378898 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0008999 absent anus IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0010413 complete atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0010466 vascular ring IAGP N RGD:5509061 20141003 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0011055 abnormal respiratory motile cilium physiology IEA N RGD:5509061 20141003 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18378898 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18378898 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16354705 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0011649 immotile respiratory cilia IEA N RGD:5509061 20141003 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0011665 d-loop transposition of the great arteries IEA N RGD:5509061 20141003 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0011872 absent xiphoid process IAGP N RGD:5509061 20231130 MGI PMID:18519639 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1552230 Pcsk5 proprotein convertase subtilisin/kexin type 5 gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:18519639 1552232 Ms4a7 membrane-spanning 4-domains, subfamily A, member 7 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20240530 MGI PMID:38478630 1552232 Ms4a7 membrane-spanning 4-domains, subfamily A, member 7 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20240530 MGI PMID:38478630 1552232 Ms4a7 membrane-spanning 4-domains, subfamily A, member 7 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20240530 MGI PMID:38478630 1552232 Ms4a7 membrane-spanning 4-domains, subfamily A, member 7 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20240530 MGI PMID:38478630 1552232 Ms4a7 membrane-spanning 4-domains, subfamily A, member 7 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20240530 MGI PMID:38478630 1552232 Ms4a7 membrane-spanning 4-domains, subfamily A, member 7 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20240530 MGI PMID:38478630 1552232 Ms4a7 membrane-spanning 4-domains, subfamily A, member 7 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20240530 MGI PMID:38478630 1552232 Ms4a7 membrane-spanning 4-domains, subfamily A, member 7 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20240530 MGI PMID:38478630 1552232 Ms4a7 membrane-spanning 4-domains, subfamily A, member 7 gene MP:0008891 decreased hepatocyte apoptosis IAGP N RGD:5509061 20240530 MGI PMID:38478630 1552232 Ms4a7 membrane-spanning 4-domains, subfamily A, member 7 gene MP:0014434 decreased cytokine level IAGP N RGD:5509061 20240530 MGI PMID:38478630 1552232 Ms4a7 membrane-spanning 4-domains, subfamily A, member 7 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240530 MGI PMID:38478630 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0003109 short femur IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0013633 decreased femur maximal load IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0013646 decreased energy dissipated prior to femur fracture IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552233 Clec11a C-type lectin domain family 11, member a gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:27976999 1552235 Panx1 pannexin 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:21606493 1552235 Panx1 pannexin 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21508259 1552235 Panx1 pannexin 1 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:21949881 1552235 Panx1 pannexin 1 gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:22384122 1552235 Panx1 pannexin 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22384122 1552235 Panx1 pannexin 1 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:22147915 1552235 Panx1 pannexin 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21949881 1552235 Panx1 pannexin 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220811 MGI 1552235 Panx1 pannexin 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:22384122 1552235 Panx1 pannexin 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210520 MGI 1552235 Panx1 pannexin 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1552235 Panx1 pannexin 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21606493 1552235 Panx1 pannexin 1 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:22147915 1552235 Panx1 pannexin 1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:22147915 1552235 Panx1 pannexin 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1552236 Or5ar1 olfactory receptor family 5 subfamily AR member 1 gene MP:0020421 increased freezing behavior IAGP N RGD:5509061 20210401 MGI PMID:28685774 1552236 Or5ar1 olfactory receptor family 5 subfamily AR member 1 gene MP:0020422 decreased freezing behavior IAGP N RGD:5509061 20210401 MGI PMID:28685774 1552237 Ihh Indian hedgehog gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:19906844 1552237 Ihh Indian hedgehog gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16278811 1552237 Ihh Indian hedgehog gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16278811 1552237 Ihh Indian hedgehog gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:16278811 1552237 Ihh Indian hedgehog gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:16278811 1552237 Ihh Indian hedgehog gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:19252479 1552237 Ihh Indian hedgehog gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15951842 1552237 Ihh Indian hedgehog gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:19906844 1552237 Ihh Indian hedgehog gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:22155527 1552237 Ihh Indian hedgehog gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10821773 1552237 Ihh Indian hedgehog gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10821773 1552237 Ihh Indian hedgehog gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:11748145 1552237 Ihh Indian hedgehog gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:16278811 1552237 Ihh Indian hedgehog gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:19906844 1552237 Ihh Indian hedgehog gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0000767 abnormal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10821773 1552237 Ihh Indian hedgehog gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:10821773 1552237 Ihh Indian hedgehog gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19906844 1552237 Ihh Indian hedgehog gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:17881493 1552237 Ihh Indian hedgehog gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:17881493 1552237 Ihh Indian hedgehog gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10821773 1552237 Ihh Indian hedgehog gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16278811 1552237 Ihh Indian hedgehog gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:11748145 1552237 Ihh Indian hedgehog gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:16278811 1552237 Ihh Indian hedgehog gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:11748145 1552237 Ihh Indian hedgehog gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:15075292 1552237 Ihh Indian hedgehog gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:19252479 1552237 Ihh Indian hedgehog gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:15075292 1552237 Ihh Indian hedgehog gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:16278811 1552237 Ihh Indian hedgehog gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:10821773 1552237 Ihh Indian hedgehog gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:11748145 1552237 Ihh Indian hedgehog gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:11748145 1552237 Ihh Indian hedgehog gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20141003 MGI PMID:10821773 1552237 Ihh Indian hedgehog gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22155527 1552237 Ihh Indian hedgehog gene MP:0003109 short femur IAGP N RGD:5509061 20171221 MGI PMID:28696225 1552237 Ihh Indian hedgehog gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17881493 1552237 Ihh Indian hedgehog gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:10821773 1552237 Ihh Indian hedgehog gene MP:0003283 abnormal digestive organ placement IAGP N RGD:5509061 20141003 MGI PMID:10821773 1552237 Ihh Indian hedgehog gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16278811 1552237 Ihh Indian hedgehog gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19252479 1552237 Ihh Indian hedgehog gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:19906844 1552237 Ihh Indian hedgehog gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11748145 1552237 Ihh Indian hedgehog gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16278811 1552237 Ihh Indian hedgehog gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22155527 1552237 Ihh Indian hedgehog gene MP:0004053 abnormal synchondrosis IAGP N RGD:5509061 20141003 MGI PMID:16278811 1552237 Ihh Indian hedgehog gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17881493 1552237 Ihh Indian hedgehog gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:10821773 1552237 Ihh Indian hedgehog gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:19906844 1552237 Ihh Indian hedgehog gene MP:0004340 short scapula IAGP N RGD:5509061 20141003 MGI PMID:11748145 1552237 Ihh Indian hedgehog gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:11748145 1552237 Ihh Indian hedgehog gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:11748145 1552237 Ihh Indian hedgehog gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20230223 MGI PMID:21364421 1552237 Ihh Indian hedgehog gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:19252479 1552237 Ihh Indian hedgehog gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0006261 annular pancreas IAGP N RGD:5509061 20141003 MGI PMID:10821773 1552237 Ihh Indian hedgehog gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:19252479 1552237 Ihh Indian hedgehog gene MP:0006322 abnormal perichondrium morphology IAGP N RGD:5509061 20141003 MGI PMID:19906844 1552237 Ihh Indian hedgehog gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:15951842 1552237 Ihh Indian hedgehog gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:16278811 1552237 Ihh Indian hedgehog gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:19906844 1552237 Ihh Indian hedgehog gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:15951842 1552237 Ihh Indian hedgehog gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16278811 1552237 Ihh Indian hedgehog gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22155527 1552237 Ihh Indian hedgehog gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:19906844 1552237 Ihh Indian hedgehog gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:22155527 1552237 Ihh Indian hedgehog gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:19252479 1552237 Ihh Indian hedgehog gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20171221 MGI PMID:28696225 1552237 Ihh Indian hedgehog gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16278811 1552237 Ihh Indian hedgehog gene MP:0010969 absent compact bone IAGP N RGD:5509061 20141003 MGI PMID:16278811 1552237 Ihh Indian hedgehog gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19906844 1552237 Ihh Indian hedgehog gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0011585 decreased alkaline phosphatase activity IAGP N RGD:5509061 20230223 MGI PMID:21364421 1552237 Ihh Indian hedgehog gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:11748145 1552237 Ihh Indian hedgehog gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:11748145 1552237 Ihh Indian hedgehog gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:15951842 1552237 Ihh Indian hedgehog gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:10465785 1552237 Ihh Indian hedgehog gene MP:0020516 abnormal visceral yolk sac mesenchyme morphology IAGP N RGD:5509061 20180125 MGI PMID:17881493 1552237 Ihh Indian hedgehog gene MP:0021208 median cleft palate IAGP N RGD:5509061 20230223 MGI PMID:21364421 1552237 Ihh Indian hedgehog gene MP:0021217 abnormal palatal shelf bone ossification IAGP N RGD:5509061 20230223 MGI PMID:21364421 1552239 H2-Q10 histocompatibility 2, Q region locus 10 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20231207 MGI 1552239 H2-Q10 histocompatibility 2, Q region locus 10 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20201029 MGI PMID:30537346 1552239 H2-Q10 histocompatibility 2, Q region locus 10 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20201029 MGI PMID:30537346 1552239 H2-Q10 histocompatibility 2, Q region locus 10 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20201029 MGI PMID:30537346 1552239 H2-Q10 histocompatibility 2, Q region locus 10 gene MP:0011625 cystolithiasis IEA N RGD:5509061 20231207 MGI 1552239 H2-Q10 histocompatibility 2, Q region locus 10 gene MP:0013666 decreased immature NK cell number IAGP N RGD:5509061 20201029 MGI PMID:30537346 1552239 H2-Q10 histocompatibility 2, Q region locus 10 gene MP:0013672 decreased mature NK cell number IAGP N RGD:5509061 20201029 MGI PMID:30537346 1552240 Gykl1 glycerol kinase-like 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:28852571 1552240 Gykl1 glycerol kinase-like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:28852571 1552240 Gykl1 glycerol kinase-like 1 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20200310 MGI PMID:28852571 1552240 Gykl1 glycerol kinase-like 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:28852571 1552240 Gykl1 glycerol kinase-like 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20200310 MGI PMID:28852571 1552240 Gykl1 glycerol kinase-like 1 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20200310 MGI PMID:28852571 1552240 Gykl1 glycerol kinase-like 1 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20200310 MGI PMID:28852571 1552240 Gykl1 glycerol kinase-like 1 gene MP:0014464 decreased sperm mitochondrial sheath size IAGP N RGD:5509061 20240613 MGI PMID:28852571 1552242 Eif2b3 eukaryotic translation initiation factor 2B, subunit 3 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1552242 Eif2b3 eukaryotic translation initiation factor 2B, subunit 3 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1552242 Eif2b3 eukaryotic translation initiation factor 2B, subunit 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552242 Eif2b3 eukaryotic translation initiation factor 2B, subunit 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1552242 Eif2b3 eukaryotic translation initiation factor 2B, subunit 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15539485 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15563592 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:15539485 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15539485 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:17275784 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15539485 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15563592 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19590036 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15539485 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19590036 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0002764 short tibia IEA N RGD:5509061 20231207 MGI 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:19590036 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20141003 MGI PMID:17275784 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:15563592 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20240523 MGI 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15539485 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20240523 MGI 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17275784 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19590036 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19590036 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:15563592 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15539485 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20240523 MGI 1552243 Mmp13 matrix metallopeptidase 13 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:15563592 1552244 Etfbkmt electron transfer flavoprotein beta subunit lysine methyltransferase gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20190307 MGI PMID:29352221 1552244 Etfbkmt electron transfer flavoprotein beta subunit lysine methyltransferase gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20190307 MGI PMID:29352221 1552244 Etfbkmt electron transfer flavoprotein beta subunit lysine methyltransferase gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20190307 MGI PMID:29352221 1552244 Etfbkmt electron transfer flavoprotein beta subunit lysine methyltransferase gene MP:0014173 increased fatty acid beta-oxidation IAGP N RGD:5509061 20190307 MGI PMID:29352221 1552244 Etfbkmt electron transfer flavoprotein beta subunit lysine methyltransferase gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20190307 MGI PMID:29352221 1552246 Rcor2 REST corepressor 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20170601 MGI PMID:26795843 1552246 Rcor2 REST corepressor 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20170601 MGI PMID:26795843 1552246 Rcor2 REST corepressor 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20170601 MGI PMID:26795843 1552246 Rcor2 REST corepressor 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20170601 MGI PMID:26795843 1552246 Rcor2 REST corepressor 2 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20170601 MGI PMID:26795843 1552246 Rcor2 REST corepressor 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20170601 MGI PMID:26795843 1552246 Rcor2 REST corepressor 2 gene MP:0009974 decreased cerebral cortex pyramidal cell number IAGP N RGD:5509061 20170601 MGI PMID:26795843 1552246 Rcor2 REST corepressor 2 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20170601 MGI PMID:26795843 1552250 Axin1 axin 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:17246824 1552250 Axin1 axin 1 gene MP:0000151 absent ribs IAGP N RGD:5509061 20200310 MGI PMID:17246824 1552250 Axin1 axin 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20200310 MGI PMID:17246824 1552250 Axin1 axin 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20200310 MGI PMID:8536979 1552250 Axin1 axin 1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0000435 shortened head IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20200310 MGI PMID:13340237 1552250 Axin1 axin 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20200310 MGI PMID:17246824 1552250 Axin1 axin 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20200310 MGI PMID:13340237 1552250 Axin1 axin 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20200310 MGI PMID:17246824 1552250 Axin1 axin 1 gene MP:0000585 kinked tail IEA N RGD:5509061 20111116 MGI 1552250 Axin1 axin 1 gene MP:0000592 short tail IAGP N RGD:5509061 20200310 MGI PMID:17246824 1552250 Axin1 axin 1 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:8536979 1552250 Axin1 axin 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20200310 MGI PMID:8536979 1552250 Axin1 axin 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:21003499 1552250 Axin1 axin 1 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20200310 MGI PMID:17246824 1552250 Axin1 axin 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0001675 abnormal ectoderm development IEA N RGD:5509061 20111116 MGI 1552250 Axin1 axin 1 gene MP:0001684 abnormal axial mesoderm morphology IAGP N RGD:5509061 20200310 MGI PMID:9230313 1552250 Axin1 axin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:21344612 1552250 Axin1 axin 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20200310 MGI PMID:18113441 1552250 Axin1 axin 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20200310 MGI PMID:8536979 1552250 Axin1 axin 1 gene MP:0001967 deafness IAGP N RGD:5509061 20200310 MGI PMID:21003499 1552250 Axin1 axin 1 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20111116 MGI 1552250 Axin1 axin 1 gene MP:0002084 abnormal developmental patterning IEA N RGD:5509061 20200310 MGI 1552250 Axin1 axin 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:18113441 1552250 Axin1 axin 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:21344612 1552250 Axin1 axin 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:8536979 1552250 Axin1 axin 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:18113441 1552250 Axin1 axin 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20200310 MGI PMID:11170344 1552250 Axin1 axin 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:17246824 1552250 Axin1 axin 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20200310 MGI PMID:13340237 1552250 Axin1 axin 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20200310 MGI PMID:21003499 1552250 Axin1 axin 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15899843 1552250 Axin1 axin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:17246824 1552250 Axin1 axin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:21344612 1552250 Axin1 axin 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:17246824 1552250 Axin1 axin 1 gene MP:0003047 abnormal thoracic vertebrae morphology IEA N RGD:5509061 20111116 MGI 1552250 Axin1 axin 1 gene MP:0003049 abnormal lumbar vertebrae morphology IEA N RGD:5509061 20111116 MGI 1552250 Axin1 axin 1 gene MP:0003050 abnormal sacral vertebrae morphology IEA N RGD:5509061 20111116 MGI 1552250 Axin1 axin 1 gene MP:0003121 genetic imprinting IAGP N RGD:5509061 20200310 MGI PMID:12601169 1552250 Axin1 axin 1 gene MP:0003121 genetic imprinting IAGP N RGD:5509061 20200310 MGI PMID:7276510 1552250 Axin1 axin 1 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20200310 MGI PMID:12601169 1552250 Axin1 axin 1 gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20200310 MGI PMID:12601169 1552250 Axin1 axin 1 gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20200310 MGI PMID:7276510 1552250 Axin1 axin 1 gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20230601 MGI PMID:24265074 1552250 Axin1 axin 1 gene MP:0003176 reversion by viral sequence excision IAGP N RGD:5509061 20200310 MGI PMID:11132407 1552250 Axin1 axin 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20200310 MGI PMID:8536979 1552250 Axin1 axin 1 gene MP:0003591 urethra atresia IAGP N RGD:5509061 20200310 MGI PMID:13340237 1552250 Axin1 axin 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20200310 MGI PMID:17246824 1552250 Axin1 axin 1 gene MP:0003722 absent ureter IAGP N RGD:5509061 20200310 MGI PMID:17246824 1552250 Axin1 axin 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:18113441 1552250 Axin1 axin 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:8536979 1552250 Axin1 axin 1 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20200310 MGI PMID:18113441 1552250 Axin1 axin 1 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20200310 MGI PMID:8536979 1552250 Axin1 axin 1 gene MP:0004619 caudal vertebral fusion IEA N RGD:5509061 20111116 MGI 1552250 Axin1 axin 1 gene MP:0004621 lumbar vertebral fusion IEA N RGD:5509061 20111116 MGI 1552250 Axin1 axin 1 gene MP:0004622 sacral vertebral fusion IEA N RGD:5509061 20111116 MGI 1552250 Axin1 axin 1 gene MP:0004623 thoracic vertebral fusion IEA N RGD:5509061 20111116 MGI 1552250 Axin1 axin 1 gene MP:0004713 split notochord IAGP N RGD:5509061 20200310 MGI PMID:18113441 1552250 Axin1 axin 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20200310 MGI PMID:21344612 1552250 Axin1 axin 1 gene MP:0009352 impaired spacing of implantation sites IEA N RGD:5509061 20111116 MGI 1552250 Axin1 axin 1 gene MP:0009353 twin decidual capsule IEA N RGD:5509061 20111116 MGI 1552250 Axin1 axin 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18113441 1552250 Axin1 axin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19204372 1552250 Axin1 axin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:8536979 1552250 Axin1 axin 1 gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20200310 MGI PMID:8536979 1552250 Axin1 axin 1 gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20200310 MGI PMID:8536979 1552250 Axin1 axin 1 gene MP:0011775 rectal atresia IAGP N RGD:5509061 20200310 MGI PMID:13340237 1552250 Axin1 axin 1 gene MP:0011999 abnormal tail length IAGP N RGD:5509061 20200310 MGI PMID:17246824 1552250 Axin1 axin 1 gene MP:0012062 small tail bud IAGP N RGD:5509061 20200310 MGI PMID:18113441 1552250 Axin1 axin 1 gene MP:0012104 small amniotic cavity IEA N RGD:5509061 20200310 MGI 1552250 Axin1 axin 1 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20200310 MGI PMID:8536979 1552250 Axin1 axin 1 gene MP:0012156 rostral-caudal axis duplication IAGP N RGD:5509061 20200310 MGI PMID:18113441 1552250 Axin1 axin 1 gene MP:0012156 rostral-caudal axis duplication IAGP N RGD:5509061 20200310 MGI PMID:8536979 1552250 Axin1 axin 1 gene MP:0012174 flat head IAGP N RGD:5509061 20200310 MGI PMID:8536979 1552250 Axin1 axin 1 gene MP:0013175 bifurcated tail IAGP N RGD:5509061 20200310 MGI PMID:17246824 1552252 Septin7 septin 7 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20150910 MGI PMID:25122120 1552252 Septin7 septin 7 gene MP:0003707 increased cell nucleus count IAGP N RGD:5509061 20150910 MGI PMID:25122120 1552252 Septin7 septin 7 gene MP:0003903 increased cell mass IAGP N RGD:5509061 20150910 MGI PMID:25122120 1552252 Septin7 septin 7 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:24113571 1552252 Septin7 septin 7 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:24113571 1552252 Septin7 septin 7 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20150910 MGI PMID:25122120 1552252 Septin7 septin 7 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20150910 MGI PMID:25122120 1552252 Septin7 septin 7 gene MP:0013289 abnormal mitotic cytokinesis IAGP N RGD:5509061 20150910 MGI PMID:25122120 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15100286 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20161216 MGI PMID:27708076 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20161216 MGI PMID:27708076 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20161216 MGI PMID:27708076 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15100286 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20161216 MGI PMID:27708076 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20190221 MGI PMID:30580966 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20180726 MGI PMID:28783703 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20180726 MGI PMID:28783703 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:8671660 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8671660 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15100286 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15100286 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:15100286 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20161216 MGI PMID:27708076 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20180726 MGI PMID:28783703 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20180726 MGI PMID:28783703 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8602528 1552253 Lag3 lymphocyte-activation gene 3 gene MP:0013762 abnormal effector T cell number IAGP N RGD:5509061 20180726 MGI PMID:28783703 1552255 Zfp410 zinc finger protein 410 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240516 MGI PMID:33859416 1552256 Adprhl1 ADP-ribosylhydrolase like 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 1552257 Ctnnd1 catenin delta 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221027 MGI PMID:29805042 1552257 Ctnnd1 catenin delta 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:18809907 1552257 Ctnnd1 catenin delta 1 gene MP:0000424 retarded hair growth IAGP N RGD:5509061 20200310 MGI PMID:18809907 1552257 Ctnnd1 catenin delta 1 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:18809907 1552257 Ctnnd1 catenin delta 1 gene MP:0001346 abnormal lacrimal gland morphology IAGP N RGD:5509061 20200310 MGI PMID:16399075 1552257 Ctnnd1 catenin delta 1 gene MP:0002235 abnormal external nares morphology IAGP N RGD:5509061 20221027 MGI PMID:29805042 1552257 Ctnnd1 catenin delta 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0003708 binucleate IAGP N RGD:5509061 20200310 MGI PMID:18809907 1552257 Ctnnd1 catenin delta 1 gene MP:0003792 abnormal major salivary gland morphology IAGP N RGD:5509061 20200310 MGI PMID:16399075 1552257 Ctnnd1 catenin delta 1 gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20200310 MGI PMID:16399075 1552257 Ctnnd1 catenin delta 1 gene MP:0004035 abnormal sublingual gland morphology IAGP N RGD:5509061 20200310 MGI PMID:16399075 1552257 Ctnnd1 catenin delta 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200310 MGI PMID:18809907 1552257 Ctnnd1 catenin delta 1 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20221027 MGI PMID:29805042 1552257 Ctnnd1 catenin delta 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20200310 MGI PMID:16815331 1552257 Ctnnd1 catenin delta 1 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0009051 dilated distal convoluted tubule IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20200310 MGI PMID:18809907 1552257 Ctnnd1 catenin delta 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221027 MGI PMID:29805042 1552257 Ctnnd1 catenin delta 1 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20200310 MGI PMID:16815331 1552257 Ctnnd1 catenin delta 1 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:18809907 1552257 Ctnnd1 catenin delta 1 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20221027 MGI PMID:29805042 1552257 Ctnnd1 catenin delta 1 gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16399075 1552257 Ctnnd1 catenin delta 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0011364 abnormal metanephros morphology IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21521738 1552257 Ctnnd1 catenin delta 1 gene MP:0013300 abnormal submandibular gland physiology IAGP N RGD:5509061 20200310 MGI PMID:16399075 1552257 Ctnnd1 catenin delta 1 gene MP:0013540 increased submandibular gland apoptosis IAGP N RGD:5509061 20200310 MGI PMID:16399075 1552257 Ctnnd1 catenin delta 1 gene MP:0021164 oral cleft IAGP N RGD:5509061 20221027 MGI PMID:29805042 1552257 Ctnnd1 catenin delta 1 gene MP:0021210 bilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:29805042 1552257 Ctnnd1 catenin delta 1 gene MP:0021211 unilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:29805042 1552257 Ctnnd1 catenin delta 1 gene MP:0030099 facial asymmetry IAGP N RGD:5509061 20221027 MGI PMID:29805042 1552257 Ctnnd1 catenin delta 1 gene MP:0030115 abnormal nasal tip morphology IAGP N RGD:5509061 20221027 MGI PMID:29805042 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20200310 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20200310 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20200310 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0001219 thick epidermis IAGP N RGD:5509061 20200310 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20200310 MGI PMID:19829704 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:19829704 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20200310 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20200310 MGI PMID:20530548 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20200310 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200310 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20200310 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20200310 MGI PMID:20530548 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20200310 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20200310 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20200310 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200310 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0004063 dilated heart left atrium IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20200310 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20200310 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20200310 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20200310 MGI PMID:19829704 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20200310 MGI PMID:19829704 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:19829704 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20200310 MGI PMID:19829704 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0010224 abnormal heart ventricle outflow tract morphology IAGP N RGD:5509061 20200310 MGI PMID:20530548 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0010574 dilated aorta IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0010591 enlarged aortic valve IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0010591 enlarged aortic valve IAGP N RGD:5509061 20231221 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20231221 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0010600 enlarged pulmonary valve IAGP N RGD:5509061 20200310 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0010600 enlarged pulmonary valve IAGP N RGD:5509061 20231221 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20231221 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0010618 enlarged mitral valve IAGP N RGD:5509061 20231221 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0010620 thick mitral valve IAGP N RGD:5509061 20231221 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0010627 enlarged tricuspid valve IAGP N RGD:5509061 20231221 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0010629 thick tricuspid valve IAGP N RGD:5509061 20231221 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:19829704 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0031550 abnormal atrioventricular valve development IAGP N RGD:5509061 20240104 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0031555 abnormal pulmonary valve development IAGP N RGD:5509061 20240104 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0031570 enlarged atrioventricular valve IAGP N RGD:5509061 20240125 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0031570 enlarged atrioventricular valve IAGP N RGD:5509061 20240125 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0031570 enlarged atrioventricular valve IAGP N RGD:5509061 20240125 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0031575 atrioventricular valve stenosis IAGP N RGD:5509061 20240125 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0031580 enlarged semilunar valve IAGP N RGD:5509061 20240125 MGI PMID:12621152 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0031580 enlarged semilunar valve IAGP N RGD:5509061 20240125 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0031580 enlarged semilunar valve IAGP N RGD:5509061 20240125 MGI PMID:14597776 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0031585 semilunar valve stenosis IAGP N RGD:5509061 20240125 MGI PMID:12773386 1552258 Hbegf heparin-binding EGF-like growth factor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:14597776 1552259 Gas7 growth arrest specific 7 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20201022 MGI 1552259 Gas7 growth arrest specific 7 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20160225 MGI PMID:22662195 1552259 Gas7 growth arrest specific 7 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20160225 MGI PMID:22662195 1552259 Gas7 growth arrest specific 7 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20160225 MGI PMID:22662195 1552259 Gas7 growth arrest specific 7 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160225 MGI PMID:22662195 1552259 Gas7 growth arrest specific 7 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1552259 Gas7 growth arrest specific 7 gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20160225 MGI PMID:22662195 1552259 Gas7 growth arrest specific 7 gene MP:0004243 abnormal motor nerve collateral sprouting IAGP N RGD:5509061 20160225 MGI PMID:22662195 1552259 Gas7 growth arrest specific 7 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1552259 Gas7 growth arrest specific 7 gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20160225 MGI PMID:22662195 1552259 Gas7 growth arrest specific 7 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20160225 MGI PMID:22662195 1552259 Gas7 growth arrest specific 7 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20181227 MGI 1552259 Gas7 growth arrest specific 7 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160225 MGI PMID:22662195 1552259 Gas7 growth arrest specific 7 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 1552260 Rpl22l1 ribosomal protein L22 like 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:28076796 1552260 Rpl22l1 ribosomal protein L22 like 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28076796 1552261 Slc45a3 solute carrier family 45, member 3 gene MP:0002833 increased heart weight IEA N RGD:5509061 20230720 MGI 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:16730350 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:16730350 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:16730350 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:16730350 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:16730350 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0003087 absent allantois IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20200310 MGI PMID:16730350 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0005030 absent amnion IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0008365 adenohypophysis hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:16730350 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0009593 absent chorion IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0011184 absent embryonic epiblast IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552262 Lin9 lin-9 DREAM MuvB core complex component gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20200310 MGI PMID:20404087 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0003402 decreased liver weight IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20230119 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20200310 MGI PMID:17463252 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0013771 decreased effector memory T-helper cell number IEA N RGD:5509061 20240523 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20200310 MGI PMID:23452856 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0020468 abnormal circadian behavior period IAGP N RGD:5509061 20200310 MGI PMID:23471982 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20200310 MGI PMID:15248865 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20200310 MGI PMID:17462724 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20200310 MGI PMID:17463252 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20200310 MGI PMID:23452855 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20200310 MGI PMID:23452856 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20200310 MGI PMID:23471982 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0020475 delayed circadian behavior phase IEA N RGD:5509061 20200310 MGI 1552263 Fbxl3 F-box and leucine-rich repeat protein 3 gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20200310 MGI PMID:23452856 1552264 Qrsl1 glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1552264 Qrsl1 glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 1552264 Qrsl1 glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20220602 MGI PMID:25481243 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20220602 MGI PMID:25481243 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20220602 MGI PMID:25481243 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20220602 MGI PMID:25481243 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20220602 MGI PMID:25481243 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20220602 MGI PMID:25481243 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20220602 MGI PMID:25481243 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:15741318 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:15741318 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:15741318 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:15741318 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20220602 MGI PMID:25481243 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:15741318 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:15741318 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0008389 hypochromic macrocytic anemia IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20220602 MGI PMID:25481243 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15741318 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20170223 MGI PMID:27622333 1552266 Sf3b1 splicing factor 3b, subunit 1 gene MP:0031392 hypoactivity IAGP N RGD:5509061 20220602 MGI PMID:25481243 1552268 Allc allantoicase gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201022 MGI PMID:32588039 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23544080 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23544080 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0000767 abnormal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:23544080 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:22781001 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23544080 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23544080 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22781001 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002223 lymphoid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:23544080 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002367 abnormal thymus lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22781001 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002534 abnormal type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23544080 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210520 MGI 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:22781001 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0003630 abnormal urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:23544080 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210520 MGI 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0004972 abnormal regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23544080 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22781001 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20190801 MGI PMID:28165339 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0006418 abnormal testis cord formation IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20190801 MGI PMID:28165339 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23544080 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20190801 MGI PMID:28165339 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:23544080 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:23544080 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0009370 decreased theca cell number IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0009895 decreased palatine bone horizontal plate size IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20141003 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:17143286 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0013591 thymus medulla hyperplasia IAGP N RGD:5509061 20150326 MGI PMID:19119317 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:19056881 1552269 Sgpl1 sphingosine phosphate lyase 1 gene MP:0030383 small presphenoid bone IAGP N RGD:5509061 20171207 MGI PMID:17143286 1552274 Nme2 NME/NM23 nucleoside diphosphate kinase 2 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20181227 MGI 1552274 Nme2 NME/NM23 nucleoside diphosphate kinase 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1552274 Nme2 NME/NM23 nucleoside diphosphate kinase 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1552274 Nme2 NME/NM23 nucleoside diphosphate kinase 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1552274 Nme2 NME/NM23 nucleoside diphosphate kinase 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1552274 Nme2 NME/NM23 nucleoside diphosphate kinase 2 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210520 MGI 1552274 Nme2 NME/NM23 nucleoside diphosphate kinase 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20884616 1552274 Nme2 NME/NM23 nucleoside diphosphate kinase 2 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:20884616 1552274 Nme2 NME/NM23 nucleoside diphosphate kinase 2 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:20884616 1552274 Nme2 NME/NM23 nucleoside diphosphate kinase 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20884616 1552274 Nme2 NME/NM23 nucleoside diphosphate kinase 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20884616 1552274 Nme2 NME/NM23 nucleoside diphosphate kinase 2 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:20884616 1552274 Nme2 NME/NM23 nucleoside diphosphate kinase 2 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:20884616 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:7683855 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:7683855 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:3783318 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:9600738 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10191135 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:3783318 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:3783318 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:3783318 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:3783318 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:3783318 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:3783318 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:3783318 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:3783318 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210520 MGI 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:3783318 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:7683855 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:9600738 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:3783318 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10191135 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:1639406 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:3783318 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:9600738 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20221215 MGI 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:1639406 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:7683855 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7683855 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8282051 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:3783318 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8282051 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:9600738 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0008455 abnormal retina rod cell inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:8282051 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:8282051 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:8282051 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:8282051 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:8282051 1552276 Cln8 CLN8 transmembrane ER and ERGIC protein gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:8282051 1552279 Adam1a a disintegrin and metallopeptidase domain 1a gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15194697 1552279 Adam1a a disintegrin and metallopeptidase domain 1a gene MP:0005410 abnormal fertilization IAGP N RGD:5509061 20141003 MGI PMID:15194697 1552279 Adam1a a disintegrin and metallopeptidase domain 1a gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:15194697 1552279 Adam1a a disintegrin and metallopeptidase domain 1a gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20200227 MGI PMID:15194697 1552280 Nefl neurofilament, light polypeptide gene MP:0000745 tremors IAGP N RGD:5509061 20160324 MGI PMID:25552649 1552280 Nefl neurofilament, light polypeptide gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20160324 MGI PMID:25552649 1552280 Nefl neurofilament, light polypeptide gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20160324 MGI PMID:25552649 1552280 Nefl neurofilament, light polypeptide gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20160324 MGI PMID:25552649 1552280 Nefl neurofilament, light polypeptide gene MP:0000958 peripheral nervous system degeneration IAGP N RGD:5509061 20141003 MGI PMID:9689132 1552280 Nefl neurofilament, light polypeptide gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20160324 MGI PMID:25552649 1552280 Nefl neurofilament, light polypeptide gene MP:0001513 limb grasping IAGP N RGD:5509061 20160324 MGI PMID:25552649 1552280 Nefl neurofilament, light polypeptide gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19116659 1552280 Nefl neurofilament, light polypeptide gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160324 MGI PMID:25552649 1552280 Nefl neurofilament, light polypeptide gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20160324 MGI PMID:25552649 1552280 Nefl neurofilament, light polypeptide gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:10461886 1552280 Nefl neurofilament, light polypeptide gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:9398473 1552280 Nefl neurofilament, light polypeptide gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:9689132 1552280 Nefl neurofilament, light polypeptide gene MP:0008503 abnormal spinal cord grey matter morphology IAGP N RGD:5509061 20160324 MGI PMID:25552649 1552280 Nefl neurofilament, light polypeptide gene MP:0014062 nervous system inclusion bodies IAGP N RGD:5509061 20160324 MGI PMID:25552649 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20211021 MGI PMID:34434211 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0000066 osteoporosis IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20200310 MGI PMID:16502419 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20200310 MGI PMID:17227850 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:10537105 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20200310 MGI PMID:22522171 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:17717145 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:10537105 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:21145943 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0001306 small lens IAGP N RGD:5509061 20200310 MGI PMID:21145943 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:9372963 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:9372963 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20211021 MGI PMID:34434211 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:10537105 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:9372963 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:22522171 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20200310 MGI PMID:17227850 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:17227850 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:21145943 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20200310 MGI PMID:17717145 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:22522171 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20200310 MGI PMID:10537105 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20200310 MGI PMID:22522171 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:10537105 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20200310 MGI PMID:10537105 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20211021 MGI PMID:34434211 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20200310 MGI PMID:17227850 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20200310 MGI PMID:17622570 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200310 MGI PMID:10537105 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200310 MGI PMID:21145943 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200310 MGI PMID:22522171 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:10537105 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:17227850 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:9372963 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20200310 MGI PMID:10537105 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20200310 MGI PMID:17717145 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0008071 absent B cells IAGP N RGD:5509061 20200310 MGI PMID:9372963 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20200310 MGI PMID:22522171 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20200310 MGI PMID:9372963 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20200310 MGI PMID:10537105 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20200310 MGI PMID:9372963 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20200310 MGI PMID:21145943 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20200310 MGI PMID:22522171 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20200310 MGI PMID:10537105 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0010537 tumor regression IAGP N RGD:5509061 20200310 MGI PMID:10537105 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20200310 MGI PMID:17227850 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20200310 MGI PMID:19956687 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9372963 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22522171 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9372963 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10537105 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21145943 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9372963 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0011140 decreased lung endothelial cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:17717145 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0011141 increased lung endothelial cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:17717145 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20200310 MGI PMID:22522171 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20211021 MGI PMID:34434211 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0014409 decreased distortion product otoacoustic emission amplitude IAGP N RGD:5509061 20240405 MGI PMID:34434211 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0020321 increased vascular endothelial cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:17717145 1552283 Id1 inhibitor of DNA binding 1, HLH protein gene MP:0030410 middle ear effusion IAGP N RGD:5509061 20211021 MGI PMID:34434211 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:10440905 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12374761 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17855597 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10440905 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10527801 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:10527801 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:12374761 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:12374761 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201210 MGI PMID:32601357 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:15326100 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:12374761 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:12374761 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17855597 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20201210 MGI PMID:32601357 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12374761 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:12374761 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:20219947 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:12374761 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:17855597 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:20219947 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12374761 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:20219947 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10527801 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17855597 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:10440905 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20201210 MGI PMID:32601357 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:12374761 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20160825 MGI PMID:27101989 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20160825 MGI PMID:27101989 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:17855597 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:20219947 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:17855597 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20201210 MGI PMID:32601357 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20160825 MGI PMID:27101989 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:12374761 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15326100 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:12374761 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:10440905 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:10527801 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17855597 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20201210 MGI PMID:32601357 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15326100 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:10527801 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20201210 MGI PMID:32601357 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:20219947 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:20219947 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10527801 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12374761 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12374761 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0008195 abnormal professional antigen presenting cell morphology IAGP N RGD:5509061 20160825 MGI PMID:27101989 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:20219947 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12374761 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20160825 MGI PMID:27101989 1552285 Cln3 CLN3 lysosomal/endosomal transmembrane protein, battenin gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20201210 MGI PMID:32601357 1552286 Nudt21 nudix hydrolase 21 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20200310 MGI PMID:30830875 1552286 Nudt21 nudix hydrolase 21 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20200310 MGI PMID:30830875 1552286 Nudt21 nudix hydrolase 21 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20200310 MGI PMID:30830875 1552286 Nudt21 nudix hydrolase 21 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552286 Nudt21 nudix hydrolase 21 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1552286 Nudt21 nudix hydrolase 21 gene MP:0020253 increased collagen level IAGP N RGD:5509061 20200310 MGI PMID:30830875 1552290 Flywch1 FLYWCH-type zinc finger 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200310 MGI 1552290 Flywch1 FLYWCH-type zinc finger 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552290 Flywch1 FLYWCH-type zinc finger 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20200402 MGI 1552292 E2f6 E2F transcription factor 6 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:12101104 1552292 E2f6 E2F transcription factor 6 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15936277 1552292 E2f6 E2F transcription factor 6 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12101104 1552292 E2f6 E2F transcription factor 6 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12101104 1552292 E2f6 E2F transcription factor 6 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12101104 1552292 E2f6 E2F transcription factor 6 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552292 E2f6 E2F transcription factor 6 gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20141003 MGI PMID:18366140 1552295 Epha8 Eph receptor A8 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:9214628 1552295 Epha8 Eph receptor A8 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:9214628 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0004757 abnormal distal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0005502 abnormal renal/urinary system physiology IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0008137 absent podocytes IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0008626 increased circulating interleukin-5 level IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0011428 decreased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10498891 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0014350 disorganized spleen B cell follicle IAGP N RGD:5509061 20240104 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0014471 enhanced B cell migration IAGP N RGD:5509061 20240613 MGI PMID:17142749 1552296 Arhgdia Rho GDP dissociation inhibitor alpha gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:10498891 1552297 Col14a1 collagen, type XIV, alpha 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19136672 1552297 Col14a1 collagen, type XIV, alpha 1 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:19136672 1552297 Col14a1 collagen, type XIV, alpha 1 gene MP:0003098 decreased tendon stiffness IAGP N RGD:5509061 20141003 MGI PMID:19136672 1552297 Col14a1 collagen, type XIV, alpha 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20201022 MGI 1552297 Col14a1 collagen, type XIV, alpha 1 gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:19136672 1552299 Tspan4 tetraspanin 4 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38786026 1552302 Hdac6 histone deacetylase 6 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18180281 1552302 Hdac6 histone deacetylase 6 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:23364049 1552302 Hdac6 histone deacetylase 6 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18180281 1552302 Hdac6 histone deacetylase 6 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:18180281 1552302 Hdac6 histone deacetylase 6 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:18180281 1552302 Hdac6 histone deacetylase 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18180281 1552302 Hdac6 histone deacetylase 6 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20151112 MGI PMID:17938201 1552302 Hdac6 histone deacetylase 6 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20160929 MGI PMID:23184605 1552302 Hdac6 histone deacetylase 6 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:23364049 1552302 Hdac6 histone deacetylase 6 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20160929 MGI PMID:23184605 1552302 Hdac6 histone deacetylase 6 gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20160225 MGI PMID:24747960 1552302 Hdac6 histone deacetylase 6 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20160225 MGI PMID:24747960 1552302 Hdac6 histone deacetylase 6 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23364049 1552302 Hdac6 histone deacetylase 6 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23364049 1552302 Hdac6 histone deacetylase 6 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:18180281 1552302 Hdac6 histone deacetylase 6 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:23364049 1552303 Colgalt2 collagen beta(1-O)galactosyltransferase 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20220203 MGI PMID:30355948 1552303 Colgalt2 collagen beta(1-O)galactosyltransferase 2 gene MP:0004941 abnormal regulatory T cell morphology IAGP N RGD:5509061 20220203 MGI PMID:30355948 1552303 Colgalt2 collagen beta(1-O)galactosyltransferase 2 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20220203 MGI PMID:30355948 1552303 Colgalt2 collagen beta(1-O)galactosyltransferase 2 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20220203 MGI PMID:30355948 1552303 Colgalt2 collagen beta(1-O)galactosyltransferase 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20220203 MGI PMID:30355948 1552303 Colgalt2 collagen beta(1-O)galactosyltransferase 2 gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20220203 MGI PMID:30355948 1552303 Colgalt2 collagen beta(1-O)galactosyltransferase 2 gene MP:0008629 increased circulating interleukin-9 level IAGP N RGD:5509061 20220203 MGI PMID:30355948 1552303 Colgalt2 collagen beta(1-O)galactosyltransferase 2 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20220203 MGI PMID:30355948 1552303 Colgalt2 collagen beta(1-O)galactosyltransferase 2 gene MP:0012773 abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20220203 MGI PMID:30355948 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0000467 abnormal esophagus morphology IEA N RGD:5509061 20200402 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0000745 tremors IEA N RGD:5509061 20170105 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20170105 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0002221 abnormal lymph organ size IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0003068 enlarged kidney IEA N RGD:5509061 20200402 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20190502 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230601 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20240523 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20200402 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230601 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20170105 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0011496 abnormal head size IEA N RGD:5509061 20201022 MGI 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0012188 increased regulatory T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24135136 1552304 Itch itchy, E3 ubiquitin protein ligase gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:19479951 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000160 kyphosis IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19479951 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19479951 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19217325 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0005014 increased B cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20150226 MGI PMID:23118208 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:19479951 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0008180 abnormal marginal zone B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19217325 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19479951 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0009709 hydrometra IEA N RGD:5509061 20230601 MGI 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19479951 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0012355 decreased prothrombin time IAGP N RGD:5509061 20150226 MGI PMID:23118208 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0012358 decreased partial thromboplastin time IAGP N RGD:5509061 20150226 MGI PMID:23118208 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0012616 increased circulating factor IX level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1552305 Mfng MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0020985 increased circulating factor XI level IAGP N RGD:5509061 20210204 MGI PMID:23118208 1552306 Prpf31 pre-mRNA processing factor 31 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:20811066 1552306 Prpf31 pre-mRNA processing factor 31 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20190502 MGI 1552306 Prpf31 pre-mRNA processing factor 31 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20811066 1552306 Prpf31 pre-mRNA processing factor 31 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20160421 MGI 1552306 Prpf31 pre-mRNA processing factor 31 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19578015 1552306 Prpf31 pre-mRNA processing factor 31 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19578015 1552307 Gpr158 G protein-coupled receptor 158 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20200310 MGI PMID:29419376 1552307 Gpr158 G protein-coupled receptor 158 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:29419376 1552307 Gpr158 G protein-coupled receptor 158 gene MP:0003247 abnormal glutaminergic neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:29419376 1552307 Gpr158 G protein-coupled receptor 158 gene MP:0010167 decreased response to stress-induced hyperthermia IAGP N RGD:5509061 20200310 MGI PMID:29419376 1552307 Gpr158 G protein-coupled receptor 158 gene MP:0011002 enhanced AMPA-mediated synaptic currents IAGP N RGD:5509061 20200310 MGI PMID:29419376 1552307 Gpr158 G protein-coupled receptor 158 gene MP:0014378 increased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:29419376 1552307 Gpr158 G protein-coupled receptor 158 gene MP:0014413 decreased depression-related behavior IAGP N RGD:5509061 20240425 MGI PMID:29419376 1552307 Gpr158 G protein-coupled receptor 158 gene MP:0020507 increased dendritic spine density IAGP N RGD:5509061 20200310 MGI PMID:29419376 1552308 Wdr76 WD repeat domain 76 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:30655611 1552311 Cdh15 cadherin 15 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12052883 1552312 Peli3 pellino 3 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20200310 MGI PMID:23042151 1552312 Peli3 pellino 3 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20200310 MGI 1552312 Peli3 pellino 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20230601 MGI 1552312 Peli3 pellino 3 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20200310 MGI 1552312 Peli3 pellino 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:23042151 1552312 Peli3 pellino 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230601 MGI 1552312 Peli3 pellino 3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230601 MGI 1552312 Peli3 pellino 3 gene MP:0011072 abnormal macrophage cytokine production IAGP N RGD:5509061 20200310 MGI PMID:23042151 1552312 Peli3 pellino 3 gene MP:0020938 decreased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:23042151 1552312 Peli3 pellino 3 gene MP:0031039 decreased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:23042151 1552314 Mettl6 methyltransferase 6, methylcytidine gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1552314 Mettl6 methyltransferase 6, methylcytidine gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20170713 MGI PMID:28655767 1552314 Mettl6 methyltransferase 6, methylcytidine gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220519 MGI 1552316 Taar3 trace amine-associated receptor 3 gene MP:0000774 decreased brain size IEA N RGD:5509061 20210520 MGI 1552316 Taar3 trace amine-associated receptor 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220811 MGI 1552316 Taar3 trace amine-associated receptor 3 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210520 MGI 1552316 Taar3 trace amine-associated receptor 3 gene MP:0002989 small kidney IEA N RGD:5509061 20220811 MGI 1552317 Chi3l1 chitinase 3 like 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19414556 1552317 Chi3l1 chitinase 3 like 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:19414556 1552317 Chi3l1 chitinase 3 like 1 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:19414556 1552317 Chi3l1 chitinase 3 like 1 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:19414556 1552317 Chi3l1 chitinase 3 like 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19414556 1552317 Chi3l1 chitinase 3 like 1 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19414556 1552317 Chi3l1 chitinase 3 like 1 gene MP:0008089 abnormal T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:19414556 1552317 Chi3l1 chitinase 3 like 1 gene MP:0008091 decreased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:19414556 1552317 Chi3l1 chitinase 3 like 1 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:19414556 1552317 Chi3l1 chitinase 3 like 1 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19414556 1552317 Chi3l1 chitinase 3 like 1 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:19414556 1552317 Chi3l1 chitinase 3 like 1 gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:19414556 1552317 Chi3l1 chitinase 3 like 1 gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19414556 1552317 Chi3l1 chitinase 3 like 1 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19414556 1552322 Cstf3 cleavage stimulation factor, 3' pre-RNA, subunit 3 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20190502 MGI 1552322 Cstf3 cleavage stimulation factor, 3' pre-RNA, subunit 3 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20190502 MGI 1552322 Cstf3 cleavage stimulation factor, 3' pre-RNA, subunit 3 gene MP:0001304 cataract IEA N RGD:5509061 20190502 MGI 1552322 Cstf3 cleavage stimulation factor, 3' pre-RNA, subunit 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1552322 Cstf3 cleavage stimulation factor, 3' pre-RNA, subunit 3 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 1552322 Cstf3 cleavage stimulation factor, 3' pre-RNA, subunit 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1552322 Cstf3 cleavage stimulation factor, 3' pre-RNA, subunit 3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1552322 Cstf3 cleavage stimulation factor, 3' pre-RNA, subunit 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1552325 Ublcp1 ubiquitin-like domain containing CTD phosphatase 1 gene MP:0000745 tremors IEA N RGD:5509061 20200310 MGI 1552325 Ublcp1 ubiquitin-like domain containing CTD phosphatase 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1552325 Ublcp1 ubiquitin-like domain containing CTD phosphatase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1552325 Ublcp1 ubiquitin-like domain containing CTD phosphatase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552326 Tacc2 transforming, acidic coiled-coil containing protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15226440 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0000263 absent organized vascular network IAGP N RGD:5509061 20141003 MGI PMID:16514057 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16514057 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:17360632 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:16514057 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:17360632 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16514057 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17360632 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:16514057 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:16514057 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:17360632 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:16514057 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17360632 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:16514057 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16514057 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16514057 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16514057 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:17360632 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:17360632 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16514057 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17360632 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16514057 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0012254 absent intersomitic vessels IAGP N RGD:5509061 20141003 MGI PMID:16514057 1552328 Ptprb protein tyrosine phosphatase receptor type B gene MP:0012270 cardiac edema IAGP N RGD:5509061 20141003 MGI PMID:21559415 1552329 Arf5 ADP-ribosylation factor 5 gene MP:0000745 tremors IAGP N RGD:5509061 20191114 MGI PMID:31201232 1552329 Arf5 ADP-ribosylation factor 5 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20191114 MGI PMID:31201232 1552329 Arf5 ADP-ribosylation factor 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20191114 MGI PMID:31201232 1552329 Arf5 ADP-ribosylation factor 5 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20191114 MGI PMID:31201232 1552329 Arf5 ADP-ribosylation factor 5 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20191114 MGI PMID:31201232 1552329 Arf5 ADP-ribosylation factor 5 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20191114 MGI PMID:31201232 1552329 Arf5 ADP-ribosylation factor 5 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20191114 MGI PMID:31201232 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:19220926 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:29720471 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20200310 MGI PMID:29720471 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20200310 MGI PMID:29720471 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:29720471 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20200310 MGI 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20200310 MGI PMID:19220926 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20200310 MGI PMID:29720471 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20200310 MGI PMID:29720471 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:2055457 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:2693209 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20200310 MGI PMID:29720471 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20200310 MGI PMID:19220926 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20200310 MGI PMID:29720471 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20200310 MGI PMID:29720471 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:19220926 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:29720471 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:29720471 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20200310 MGI PMID:19220926 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20200310 MGI PMID:29720471 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20200310 MGI PMID:29720471 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20200310 MGI PMID:29720471 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200310 MGI PMID:19220926 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20200310 MGI PMID:19220926 1552331 Tpi1 triosephosphate isomerase 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:2693209 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20181227 MGI 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191205 MGI 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191205 MGI 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191205 MGI 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191205 MGI 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0009331 absent primitive node IEA N RGD:5509061 20191205 MGI 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0009476 enlarged cecum IEA N RGD:5509061 20181227 MGI 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200409 MGI PMID:29479578 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200409 MGI PMID:29479578 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0012724 absent head fold IEA N RGD:5509061 20191205 MGI 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191205 MGI 1552332 Ap2s1 adaptor-related protein complex 2, sigma 1 subunit gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1552333 Cnksr2 connector enhancer of kinase suppressor of Ras 2 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1552333 Cnksr2 connector enhancer of kinase suppressor of Ras 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220519 MGI 1552333 Cnksr2 connector enhancer of kinase suppressor of Ras 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20240523 MGI 1552334 Rhot2 ras homolog family member T2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1552334 Rhot2 ras homolog family member T2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170817 MGI PMID:27705781 1552334 Rhot2 ras homolog family member T2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 1552334 Rhot2 ras homolog family member T2 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20160804 MGI 1552334 Rhot2 ras homolog family member T2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160804 MGI 1552336 Msh5 mutS homolog 5 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1552336 Msh5 mutS homolog 5 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1552336 Msh5 mutS homolog 5 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:10072381 1552336 Msh5 mutS homolog 5 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20220421 MGI PMID:28175301 1552336 Msh5 mutS homolog 5 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9916805 1552336 Msh5 mutS homolog 5 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20220811 MGI 1552336 Msh5 mutS homolog 5 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1552336 Msh5 mutS homolog 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10072381 1552336 Msh5 mutS homolog 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10809667 1552336 Msh5 mutS homolog 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9916805 1552336 Msh5 mutS homolog 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10072381 1552336 Msh5 mutS homolog 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10809667 1552336 Msh5 mutS homolog 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9916805 1552336 Msh5 mutS homolog 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20220421 MGI PMID:28175301 1552336 Msh5 mutS homolog 5 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141120 MGI PMID:9916805 1552336 Msh5 mutS homolog 5 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:10072381 1552336 Msh5 mutS homolog 5 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:10072381 1552336 Msh5 mutS homolog 5 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20220421 MGI PMID:28175301 1552336 Msh5 mutS homolog 5 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20220421 MGI PMID:28175301 1552336 Msh5 mutS homolog 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10072381 1552336 Msh5 mutS homolog 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:10072381 1552336 Msh5 mutS homolog 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:9916805 1552336 Msh5 mutS homolog 5 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:10072381 1552336 Msh5 mutS homolog 5 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:9916805 1552336 Msh5 mutS homolog 5 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:10809667 1552336 Msh5 mutS homolog 5 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:9916805 1552336 Msh5 mutS homolog 5 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:9916805 1552336 Msh5 mutS homolog 5 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:10072381 1552336 Msh5 mutS homolog 5 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20220623 MGI PMID:21915857 1552336 Msh5 mutS homolog 5 gene MP:0011896 increased circulating unsaturated transferrin level IEA N RGD:5509061 20211021 MGI 1552336 Msh5 mutS homolog 5 gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20180111 MGI PMID:21915857 1552336 Msh5 mutS homolog 5 gene MP:0013236 ovary degeneration IAGP N RGD:5509061 20141120 MGI PMID:9916805 1552336 Msh5 mutS homolog 5 gene MP:0013605 abnormal ovarian bursa morphology IAGP N RGD:5509061 20150312 MGI PMID:9916805 1552336 Msh5 mutS homolog 5 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:10072381 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0001260 increased body weight IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0001264 increased body size IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0005386 behavior/neurological phenotype IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0012006 abnormal hippocampus physiology IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0020520 whitened brown adipose tissue morphology IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0031271 increased susceptibility to age-related hepatic steatosis IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552339 Saraf store-operated calcium entry-associated regulatory factor gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20231019 MGI PMID:37007714 1552341 Ttc1 tetratricopeptide repeat domain 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210826 MGI 1552341 Ttc1 tetratricopeptide repeat domain 1 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241003 MGI 1552341 Ttc1 tetratricopeptide repeat domain 1 gene MP:0002718 abnormal inner cell mass morphology IEA N RGD:5509061 20241003 MGI 1552341 Ttc1 tetratricopeptide repeat domain 1 gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20210520 MGI 1552341 Ttc1 tetratricopeptide repeat domain 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1552341 Ttc1 tetratricopeptide repeat domain 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1552341 Ttc1 tetratricopeptide repeat domain 1 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241003 MGI 1552342 Cd302 CD302 antigen gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20210805 MGI PMID:27316686 1552342 Cd302 CD302 antigen gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20210805 MGI PMID:27316686 1552342 Cd302 CD302 antigen gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20210805 MGI PMID:27316686 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22174130 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0000495 abnormal colon morphology IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0000599 enlarged liver IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22174130 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22174130 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0000706 small thymus IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20231207 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22174130 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:22174130 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:22174130 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:22174130 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002637 small uterus IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20230601 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002981 increased liver weight IEA N RGD:5509061 20231207 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:22174130 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20211021 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20231207 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20231207 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:22174130 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22174130 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0009483 enlarged ileum IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22174130 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210520 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22174130 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20231207 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22174130 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0011503 distended jejunum IEA N RGD:5509061 20230119 MGI 1552344 Slc29a3 solute carrier family 29 (nucleoside transporters), member 3 gene MP:0011882 enlarged duodenum IEA N RGD:5509061 20230119 MGI 1552346 Ffar2 free fatty acid receptor 2 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0001553 abnormal circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18499755 1552346 Ffar2 free fatty acid receptor 2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:19865172 1552346 Ffar2 free fatty acid receptor 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160602 MGI PMID:25581519 1552346 Ffar2 free fatty acid receptor 2 gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19865172 1552346 Ffar2 free fatty acid receptor 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:19865172 1552346 Ffar2 free fatty acid receptor 2 gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:19865172 1552346 Ffar2 free fatty acid receptor 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20160602 MGI PMID:25581519 1552346 Ffar2 free fatty acid receptor 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22190648 1552346 Ffar2 free fatty acid receptor 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1552346 Ffar2 free fatty acid receptor 2 gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20160602 MGI PMID:25581519 1552346 Ffar2 free fatty acid receptor 2 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:19865172 1552346 Ffar2 free fatty acid receptor 2 gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19865172 1552346 Ffar2 free fatty acid receptor 2 gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20160602 MGI PMID:25581519 1552346 Ffar2 free fatty acid receptor 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22190648 1552346 Ffar2 free fatty acid receptor 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 1552346 Ffar2 free fatty acid receptor 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:19865172 1552346 Ffar2 free fatty acid receptor 2 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:19865172 1552346 Ffar2 free fatty acid receptor 2 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19865172 1552346 Ffar2 free fatty acid receptor 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19917676 1552346 Ffar2 free fatty acid receptor 2 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:22190648 1552347 Creb3l1 cAMP responsive element binding protein 3-like 1 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:19767743 1552347 Creb3l1 cAMP responsive element binding protein 3-like 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19767743 1552347 Creb3l1 cAMP responsive element binding protein 3-like 1 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:19767743 1552347 Creb3l1 cAMP responsive element binding protein 3-like 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19767743 1552347 Creb3l1 cAMP responsive element binding protein 3-like 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:19767743 1552347 Creb3l1 cAMP responsive element binding protein 3-like 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1552347 Creb3l1 cAMP responsive element binding protein 3-like 1 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:19767743 1552347 Creb3l1 cAMP responsive element binding protein 3-like 1 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:19767743 1552347 Creb3l1 cAMP responsive element binding protein 3-like 1 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:19767743 1552347 Creb3l1 cAMP responsive element binding protein 3-like 1 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:19767743 1552347 Creb3l1 cAMP responsive element binding protein 3-like 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:19767743 1552349 Rhbg Rhesus blood group-associated B glycoprotein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16077082 1552349 Rhbg Rhesus blood group-associated B glycoprotein gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20201022 MGI 1552349 Rhbg Rhesus blood group-associated B glycoprotein gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20211021 MGI 1552349 Rhbg Rhesus blood group-associated B glycoprotein gene MP:0011736 decreased urine ammonia level IAGP N RGD:5509061 20141003 MGI PMID:20719974 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20210114 MGI PMID:32702291 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20210114 MGI PMID:32702291 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20210114 MGI PMID:32702291 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20210114 MGI PMID:32702291 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0001712 abnormal placenta development IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0003717 pallor IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20210114 MGI PMID:32702291 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20210114 MGI PMID:32702291 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20221215 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20210114 MGI PMID:32702291 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20210114 MGI PMID:32702291 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20210114 MGI PMID:32702291 1552350 Ankmy2 ankyrin repeat and MYND domain containing 2 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220811 MGI 1552352 Dck deoxycytidine kinase gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22407915 1552352 Dck deoxycytidine kinase gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:22407915 1552352 Dck deoxycytidine kinase gene MP:0001606 impaired hematopoiesis IEA N RGD:5509061 20161201 MGI 1552352 Dck deoxycytidine kinase gene MP:0001805 decreased IgG level IEA N RGD:5509061 20161201 MGI 1552352 Dck deoxycytidine kinase gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22407915 1552352 Dck deoxycytidine kinase gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22407915 1552352 Dck deoxycytidine kinase gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1552352 Dck deoxycytidine kinase gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0002497 increased IgE level IEA N RGD:5509061 20161201 MGI 1552352 Dck deoxycytidine kinase gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22407915 1552352 Dck deoxycytidine kinase gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22407915 1552352 Dck deoxycytidine kinase gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:22407915 1552352 Dck deoxycytidine kinase gene MP:0005046 absent spleen white pulp IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22407915 1552352 Dck deoxycytidine kinase gene MP:0005425 increased macrophage cell number IEA N RGD:5509061 20161201 MGI 1552352 Dck deoxycytidine kinase gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22407915 1552352 Dck deoxycytidine kinase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22407915 1552352 Dck deoxycytidine kinase gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20161201 MGI 1552352 Dck deoxycytidine kinase gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22407915 1552352 Dck deoxycytidine kinase gene MP:0008463 abnormal peripheral lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:20080663 1552352 Dck deoxycytidine kinase gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22407915 1552352 Dck deoxycytidine kinase gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22407915 1552352 Dck deoxycytidine kinase gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20161201 MGI 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0000771 abnormal brain size IAGP N RGD:5509061 20200310 MGI PMID:17998335 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0001177 atelectasis IAGP N RGD:5509061 20200310 MGI PMID:17998335 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:17998335 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:17998335 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:16880526 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:17998335 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20200310 MGI PMID:16880526 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20200310 MGI PMID:16880526 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:17998335 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:16880526 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200310 MGI PMID:17998335 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20200310 MGI PMID:16880526 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20200310 MGI PMID:17998335 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20200310 MGI 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20200310 MGI 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200310 MGI PMID:17998335 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:17998335 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:16880526 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17998335 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16880526 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16880526 1552356 Fbxw8 F-box and WD-40 domain protein 8 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552359 Usp13 ubiquitin specific peptidase 13 (isopeptidase T-3) gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200521 MGI PMID:31204278 1552359 Usp13 ubiquitin specific peptidase 13 (isopeptidase T-3) gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200521 MGI PMID:31204278 1552359 Usp13 ubiquitin specific peptidase 13 (isopeptidase T-3) gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1552359 Usp13 ubiquitin specific peptidase 13 (isopeptidase T-3) gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20200521 MGI PMID:31204278 1552359 Usp13 ubiquitin specific peptidase 13 (isopeptidase T-3) gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20200521 MGI PMID:31204278 1552359 Usp13 ubiquitin specific peptidase 13 (isopeptidase T-3) gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20200521 MGI PMID:31204278 1552359 Usp13 ubiquitin specific peptidase 13 (isopeptidase T-3) gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1552363 Cd276 CD276 antigen gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1552363 Cd276 CD276 antigen gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12925852 1552363 Cd276 CD276 antigen gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1552363 Cd276 CD276 antigen gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15682454 1552363 Cd276 CD276 antigen gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20170209 MGI PMID:26065426 1552363 Cd276 CD276 antigen gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:12925852 1552363 Cd276 CD276 antigen gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12925852 1552363 Cd276 CD276 antigen gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20170209 MGI PMID:26065426 1552363 Cd276 CD276 antigen gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12925852 1552363 Cd276 CD276 antigen gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:12925852 1552363 Cd276 CD276 antigen gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20170209 MGI PMID:26065426 1552363 Cd276 CD276 antigen gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20170209 MGI PMID:26065426 1552363 Cd276 CD276 antigen gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 1552363 Cd276 CD276 antigen gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20170209 MGI PMID:26065426 1552363 Cd276 CD276 antigen gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:15682454 1552363 Cd276 CD276 antigen gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12925852 1552363 Cd276 CD276 antigen gene MP:0010222 abnormal T-helper 17 cell physiology IAGP N RGD:5509061 20170209 MGI PMID:26065426 1552365 Cdk9 cyclin dependent kinase 9 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1552365 Cdk9 cyclin dependent kinase 9 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1552365 Cdk9 cyclin dependent kinase 9 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220519 MGI 1552365 Cdk9 cyclin dependent kinase 9 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170105 MGI 1552365 Cdk9 cyclin dependent kinase 9 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20170105 MGI 1552365 Cdk9 cyclin dependent kinase 9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552365 Cdk9 cyclin dependent kinase 9 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1552365 Cdk9 cyclin dependent kinase 9 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1552366 Ntsr1 neurotensin receptor 1 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:12384239 1552366 Ntsr1 neurotensin receptor 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:12384239 1552366 Ntsr1 neurotensin receptor 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:11752130 1552366 Ntsr1 neurotensin receptor 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20200310 MGI PMID:12384239 1552366 Ntsr1 neurotensin receptor 1 gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20200310 MGI PMID:19596359 1552366 Ntsr1 neurotensin receptor 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20200310 MGI PMID:19596359 1552366 Ntsr1 neurotensin receptor 1 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20200310 MGI PMID:19223157 1552366 Ntsr1 neurotensin receptor 1 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20200310 MGI PMID:15030383 1552366 Ntsr1 neurotensin receptor 1 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20200310 MGI PMID:11752130 1552366 Ntsr1 neurotensin receptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:14725975 1552366 Ntsr1 neurotensin receptor 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20200310 MGI PMID:19223157 1552366 Ntsr1 neurotensin receptor 1 gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20200310 MGI PMID:19223157 1552366 Ntsr1 neurotensin receptor 1 gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20200310 MGI PMID:19596359 1552366 Ntsr1 neurotensin receptor 1 gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20200310 MGI PMID:11752130 1552366 Ntsr1 neurotensin receptor 1 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20200310 MGI PMID:12384239 1552366 Ntsr1 neurotensin receptor 1 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20200310 MGI PMID:11752130 1552367 Wbp2 WW domain binding protein 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20170202 MGI PMID:26881968 1552367 Wbp2 WW domain binding protein 2 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20160804 MGI 1552367 Wbp2 WW domain binding protein 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1552367 Wbp2 WW domain binding protein 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160804 MGI 1552367 Wbp2 WW domain binding protein 2 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20170202 MGI PMID:26881968 1552367 Wbp2 WW domain binding protein 2 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20170202 MGI PMID:26881968 1552367 Wbp2 WW domain binding protein 2 gene MP:0004746 abnormal cochlear IHC afferent innervation pattern IAGP N RGD:5509061 20170202 MGI PMID:26881968 1552367 Wbp2 WW domain binding protein 2 gene MP:0004747 abnormal cochlear OHC afferent innervation pattern IAGP N RGD:5509061 20170202 MGI PMID:26881968 1552367 Wbp2 WW domain binding protein 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1552367 Wbp2 WW domain binding protein 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160804 MGI 1552367 Wbp2 WW domain binding protein 2 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20160804 MGI 1552367 Wbp2 WW domain binding protein 2 gene MP:0006388 abnormal auditory summating potential IAGP N RGD:5509061 20170202 MGI PMID:26881968 1552367 Wbp2 WW domain binding protein 2 gene MP:0008805 decreased circulating amylase level IAGP N RGD:5509061 20170202 MGI PMID:26881968 1552367 Wbp2 WW domain binding protein 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20160804 MGI 1552367 Wbp2 WW domain binding protein 2 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20170202 MGI PMID:26881968 1552367 Wbp2 WW domain binding protein 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20170202 MGI PMID:26881968 1552368 Cyb561d2 cytochrome b-561 domain containing 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1552368 Cyb561d2 cytochrome b-561 domain containing 2 gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20220811 MGI 1552370 Tpbg trophoblast glycoprotein gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:20376365 1552370 Tpbg trophoblast glycoprotein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20376365 1552370 Tpbg trophoblast glycoprotein gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:17507657 1552370 Tpbg trophoblast glycoprotein gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:20376365 1552370 Tpbg trophoblast glycoprotein gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17507657 1552372 Hace1 HECT domain and ankyrin repeat containing, E3 ubiquitin protein ligase 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17694067 1552372 Hace1 HECT domain and ankyrin repeat containing, E3 ubiquitin protein ligase 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17694067 1552372 Hace1 HECT domain and ankyrin repeat containing, E3 ubiquitin protein ligase 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17694067 1552372 Hace1 HECT domain and ankyrin repeat containing, E3 ubiquitin protein ligase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552372 Hace1 HECT domain and ankyrin repeat containing, E3 ubiquitin protein ligase 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0002083 premature death IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0002176 increased brain weight IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0012066 decreased astrocyte number IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552374 Prrc2a proline-rich coiled-coil 2A gene MP:0013438 dysmyelination IAGP N RGD:5509061 20210805 MGI PMID:30514900 1552380 Podxl2 podocalyxin-like 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1552380 Podxl2 podocalyxin-like 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200310 MGI 1552380 Podxl2 podocalyxin-like 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200310 MGI 1552380 Podxl2 podocalyxin-like 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1552380 Podxl2 podocalyxin-like 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200310 MGI 1552380 Podxl2 podocalyxin-like 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20200310 MGI 1552380 Podxl2 podocalyxin-like 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20210603 MGI PMID:27542690 1552383 Chst7 carbohydrate sulfotransferase 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20191017 MGI PMID:30867513 1552385 Mrps12 mitochondrial ribosomal protein S12 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20220120 MGI PMID:31721250 1552385 Mrps12 mitochondrial ribosomal protein S12 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1552385 Mrps12 mitochondrial ribosomal protein S12 gene MP:0002188 small heart IAGP N RGD:5509061 20220120 MGI PMID:31721250 1552385 Mrps12 mitochondrial ribosomal protein S12 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20220120 MGI PMID:31721250 1552385 Mrps12 mitochondrial ribosomal protein S12 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20220120 MGI PMID:31721250 1552385 Mrps12 mitochondrial ribosomal protein S12 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20220120 MGI PMID:31721250 1552385 Mrps12 mitochondrial ribosomal protein S12 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20220120 MGI PMID:31721250 1552385 Mrps12 mitochondrial ribosomal protein S12 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20220120 MGI PMID:31721250 1552385 Mrps12 mitochondrial ribosomal protein S12 gene MP:0010578 abnormal heart left ventricle size IAGP N RGD:5509061 20220120 MGI PMID:31721250 1552385 Mrps12 mitochondrial ribosomal protein S12 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20220120 MGI PMID:31721250 1552385 Mrps12 mitochondrial ribosomal protein S12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552385 Mrps12 mitochondrial ribosomal protein S12 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20220120 MGI PMID:31721250 1552385 Mrps12 mitochondrial ribosomal protein S12 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1552385 Mrps12 mitochondrial ribosomal protein S12 gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20220120 MGI PMID:31721250 1552386 Tlr6 toll-like receptor 6 gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 1552386 Tlr6 toll-like receptor 6 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:16832055 1552386 Tlr6 toll-like receptor 6 gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:16832055 1552386 Tlr6 toll-like receptor 6 gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:16832055 1552386 Tlr6 toll-like receptor 6 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11431423 1552386 Tlr6 toll-like receptor 6 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16832055 1552386 Tlr6 toll-like receptor 6 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11431423 1552386 Tlr6 toll-like receptor 6 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:11431423 1552386 Tlr6 toll-like receptor 6 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:11431423 1552386 Tlr6 toll-like receptor 6 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:11431423 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20200310 MGI PMID:16717184 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20200310 MGI PMID:16717184 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:16717184 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20200310 MGI PMID:16717184 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:16103361 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:16103361 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200310 MGI PMID:16717184 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:16717184 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200310 MGI PMID:17210641 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20200310 MGI PMID:16717184 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:24567531 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:16717184 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20200310 MGI PMID:16717184 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:17210641 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:24567531 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:16717184 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200310 MGI PMID:17210641 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:24567531 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200310 MGI PMID:16717184 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20200310 MGI PMID:17210641 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20200310 MGI PMID:24567531 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:16717184 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:17210641 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16103361 1552388 Acaca acetyl-Coenzyme A carboxylase alpha gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20200310 MGI PMID:24567531 1552392 Zfp629 zinc finger protein 629 gene MP:0000692 small spleen IEA N RGD:5509061 20220519 MGI 1552392 Zfp629 zinc finger protein 629 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1552392 Zfp629 zinc finger protein 629 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1552392 Zfp629 zinc finger protein 629 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 1552392 Zfp629 zinc finger protein 629 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1552396 Slc30a3 solute carrier family 30 (zinc transporter), member 3 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9990090 1552396 Slc30a3 solute carrier family 30 (zinc transporter), member 3 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:12032347 1552396 Slc30a3 solute carrier family 30 (zinc transporter), member 3 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9990090 1552396 Slc30a3 solute carrier family 30 (zinc transporter), member 3 gene MP:0009615 abnormal zinc homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9990090 1552396 Slc30a3 solute carrier family 30 (zinc transporter), member 3 gene MP:0009617 decreased brain zinc level IAGP N RGD:5509061 20141003 MGI PMID:12032347 1552396 Slc30a3 solute carrier family 30 (zinc transporter), member 3 gene MP:0009617 decreased brain zinc level IAGP N RGD:5509061 20141003 MGI PMID:9990090 1552398 Prlhr prolactin releasing hormone receptor gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17904108 1552398 Prlhr prolactin releasing hormone receptor gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:17904108 1552398 Prlhr prolactin releasing hormone receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17904108 1552398 Prlhr prolactin releasing hormone receptor gene MP:0001432 abnormal food preference IAGP N RGD:5509061 20141003 MGI PMID:14742914 1552398 Prlhr prolactin releasing hormone receptor gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17904108 1552398 Prlhr prolactin releasing hormone receptor gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:17904108 1552398 Prlhr prolactin releasing hormone receptor gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:16299503 1552398 Prlhr prolactin releasing hormone receptor gene MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:16299503 1552398 Prlhr prolactin releasing hormone receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14742914 1552398 Prlhr prolactin releasing hormone receptor gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:16299503 1552398 Prlhr prolactin releasing hormone receptor gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:16299503 1552398 Prlhr prolactin releasing hormone receptor gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17904108 1552398 Prlhr prolactin releasing hormone receptor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:14742914 1552398 Prlhr prolactin releasing hormone receptor gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:14742914 1552398 Prlhr prolactin releasing hormone receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17904108 1552398 Prlhr prolactin releasing hormone receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17904108 1552398 Prlhr prolactin releasing hormone receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17904108 1552398 Prlhr prolactin releasing hormone receptor gene MP:0009713 enhanced conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:16299503 1552398 Prlhr prolactin releasing hormone receptor gene MP:0009776 decreased behavioral withdrawal response IAGP N RGD:5509061 20141003 MGI PMID:16299503 1552398 Prlhr prolactin releasing hormone receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17904108 1552398 Prlhr prolactin releasing hormone receptor gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:17904108 1552399 Rap1a RAS-related protein 1a gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18305243 1552399 Rap1a RAS-related protein 1a gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18305243 1552399 Rap1a RAS-related protein 1a gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18056377 1552399 Rap1a RAS-related protein 1a gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:18056377 1552399 Rap1a RAS-related protein 1a gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:18305243 1552399 Rap1a RAS-related protein 1a gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:18305243 1552399 Rap1a RAS-related protein 1a gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:18056377 1552399 Rap1a RAS-related protein 1a gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:16382154 1552399 Rap1a RAS-related protein 1a gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18305243 1552399 Rap1a RAS-related protein 1a gene MP:0004494 abnormal synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:18305243 1552399 Rap1a RAS-related protein 1a gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16382154 1552399 Rap1a RAS-related protein 1a gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18625726 1552399 Rap1a RAS-related protein 1a gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:16382154 1552399 Rap1a RAS-related protein 1a gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18056377 1552400 Notch3 notch 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200402 MGI PMID:30042232 1552400 Notch3 notch 3 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20200402 MGI PMID:30042232 1552400 Notch3 notch 3 gene MP:0000160 kyphosis IEA N RGD:5509061 20141003 MGI 1552400 Notch3 notch 3 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1552400 Notch3 notch 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21562564 1552400 Notch3 notch 3 gene MP:0000262 poor arterial differentiation IAGP N RGD:5509061 20141003 MGI PMID:15545631 1552400 Notch3 notch 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1552400 Notch3 notch 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1552400 Notch3 notch 3 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15525534 1552400 Notch3 notch 3 gene MP:0000648 absent sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:15525534 1552400 Notch3 notch 3 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:21562564 1552400 Notch3 notch 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21562564 1552400 Notch3 notch 3 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:15882997 1552400 Notch3 notch 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:15882997 1552400 Notch3 notch 3 gene MP:0000751 myopathy IEA N RGD:5509061 20141003 MGI 1552400 Notch3 notch 3 gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:21940951 1552400 Notch3 notch 3 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19897741 1552400 Notch3 notch 3 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:15525534 1552400 Notch3 notch 3 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:15525534 1552400 Notch3 notch 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200402 MGI PMID:30042232 1552400 Notch3 notch 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21940951 1552400 Notch3 notch 3 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:21940951 1552400 Notch3 notch 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:14595837 1552400 Notch3 notch 3 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20141003 MGI 1552400 Notch3 notch 3 gene MP:0001925 male infertility IEA N RGD:5509061 20141003 MGI 1552400 Notch3 notch 3 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21562564 1552400 Notch3 notch 3 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:21940951 1552400 Notch3 notch 3 gene MP:0002083 premature death IEA N RGD:5509061 20141003 MGI 1552400 Notch3 notch 3 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:14595837 1552400 Notch3 notch 3 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:14595837 1552400 Notch3 notch 3 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21562564 1552400 Notch3 notch 3 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:15545631 1552400 Notch3 notch 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1552400 Notch3 notch 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14595837 1552400 Notch3 notch 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15645445 1552400 Notch3 notch 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21991352 1552400 Notch3 notch 3 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:21940951 1552400 Notch3 notch 3 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15545631 1552400 Notch3 notch 3 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21940951 1552400 Notch3 notch 3 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20160609 MGI PMID:26563570 1552400 Notch3 notch 3 gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 1552400 Notch3 notch 3 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20200402 MGI PMID:30042232 1552400 Notch3 notch 3 gene MP:0003044 impaired basement membrane formation IAGP N RGD:5509061 20160609 MGI PMID:26563570 1552400 Notch3 notch 3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20170105 MGI 1552400 Notch3 notch 3 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:18347334 1552400 Notch3 notch 3 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:21555590 1552400 Notch3 notch 3 gene MP:0003402 decreased liver weight IEA N RGD:5509061 20210128 MGI 1552400 Notch3 notch 3 gene MP:0003554 phimosis IEA N RGD:5509061 20141003 MGI 1552400 Notch3 notch 3 gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20160609 MGI PMID:26563570 1552400 Notch3 notch 3 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20231207 MGI 1552400 Notch3 notch 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14595837 1552400 Notch3 notch 3 gene MP:0004125 abnormal venule morphology IAGP N RGD:5509061 20160609 MGI PMID:26563570 1552400 Notch3 notch 3 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1552400 Notch3 notch 3 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20200402 MGI PMID:30042232 1552400 Notch3 notch 3 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20200402 MGI PMID:30042232 1552400 Notch3 notch 3 gene MP:0005150 cachexia IEA N RGD:5509061 20141003 MGI 1552400 Notch3 notch 3 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20160211 MGI 1552400 Notch3 notch 3 gene MP:0005532 abnormal vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:15545631 1552400 Notch3 notch 3 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15545631 1552400 Notch3 notch 3 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21555590 1552400 Notch3 notch 3 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20160609 MGI PMID:26563570 1552400 Notch3 notch 3 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:19897741 1552400 Notch3 notch 3 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:18347334 1552400 Notch3 notch 3 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:18347334 1552400 Notch3 notch 3 gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20160609 MGI PMID:26563570 1552400 Notch3 notch 3 gene MP:0006325 impaired hearing IEA N RGD:5509061 20141003 MGI 1552400 Notch3 notch 3 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20200402 MGI PMID:30042232 1552400 Notch3 notch 3 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:21562564 1552400 Notch3 notch 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1552400 Notch3 notch 3 gene MP:0009417 skeletal muscle atrophy IEA N RGD:5509061 20141003 MGI 1552400 Notch3 notch 3 gene MP:0009661 abnormal pregnancy IEA N RGD:5509061 20141003 MGI 1552400 Notch3 notch 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18347334 1552400 Notch3 notch 3 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1552400 Notch3 notch 3 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20160609 MGI PMID:26563570 1552400 Notch3 notch 3 gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24100291 1552400 Notch3 notch 3 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20200402 MGI PMID:30042232 1552400 Notch3 notch 3 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20200402 MGI PMID:30042232 1552400 Notch3 notch 3 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20200402 MGI PMID:30042232 1552400 Notch3 notch 3 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20200402 MGI PMID:30042232 1552400 Notch3 notch 3 gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20200402 MGI PMID:30042232 1552400 Notch3 notch 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19897741 1552400 Notch3 notch 3 gene MP:0011181 increased hematopoietic cell number IAGP N RGD:5509061 20141003 MGI PMID:21562564 1552400 Notch3 notch 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20141003 MGI 1552400 Notch3 notch 3 gene MP:0013925 abnormal vascular plexus formation IAGP N RGD:5509061 20160609 MGI PMID:26563570 1552400 Notch3 notch 3 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20200402 MGI PMID:30042232 1552400 Notch3 notch 3 gene MP:0021002 brain lesion IAGP N RGD:5509061 20210805 MGI PMID:21940951 1552400 Notch3 notch 3 gene MP:0030438 increased osteoblast proliferation IAGP N RGD:5509061 20200402 MGI PMID:30042232 1552400 Notch3 notch 3 gene MP:0030482 increased osteocyte number IAGP N RGD:5509061 20200402 MGI PMID:30042232 1552400 Notch3 notch 3 gene MP:0031168 abnormal brain thrombosis IAGP N RGD:5509061 20201210 MGI PMID:21940951 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:10798394 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:15186781 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17537788 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:18353676 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:21147989 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:21613506 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:23035080 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:10798394 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:15186782 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19186165 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:15186782 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:15186782 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:21147989 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15186782 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:21646512 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:10798394 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17537788 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10798394 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17521568 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21147989 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23035080 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:21646512 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0009946 abnormal olfactory bulb layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21147989 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21147989 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0010057 abnormal olfactory bulb outer nerve layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21147989 1552401 Or8a1b olfactory receptor family 8 subfamily A member 1B gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15186781 1552402 Cldn18 claudin 18 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552402 Cldn18 claudin 18 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552402 Cldn18 claudin 18 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552402 Cldn18 claudin 18 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1552402 Cldn18 claudin 18 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20181227 MGI 1552402 Cldn18 claudin 18 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552402 Cldn18 claudin 18 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552402 Cldn18 claudin 18 gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552402 Cldn18 claudin 18 gene MP:0004882 enlarged lung IEA N RGD:5509061 20210128 MGI 1552402 Cldn18 claudin 18 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552402 Cldn18 claudin 18 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552402 Cldn18 claudin 18 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552402 Cldn18 claudin 18 gene MP:0005630 increased lung weight IEA N RGD:5509061 20201022 MGI 1552402 Cldn18 claudin 18 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20160707 MGI PMID:24787463 1552402 Cldn18 claudin 18 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552402 Cldn18 claudin 18 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552402 Cldn18 claudin 18 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1552402 Cldn18 claudin 18 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552402 Cldn18 claudin 18 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552402 Cldn18 claudin 18 gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20160707 MGI PMID:24787463 1552402 Cldn18 claudin 18 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552402 Cldn18 claudin 18 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552402 Cldn18 claudin 18 gene MP:0010898 abnormal pulmonary alveolus epithelium morphology IAGP N RGD:5509061 20160707 MGI PMID:24787463 1552402 Cldn18 claudin 18 gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20160707 MGI PMID:24787463 1552402 Cldn18 claudin 18 gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:23299504 1552406 Ahi1 Abelson helper integration site 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:21623382 1552406 Ahi1 Abelson helper integration site 1 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21623382 1552406 Ahi1 Abelson helper integration site 1 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:21623382 1552406 Ahi1 Abelson helper integration site 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21623382 1552406 Ahi1 Abelson helper integration site 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20081859 1552406 Ahi1 Abelson helper integration site 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19718039 1552406 Ahi1 Abelson helper integration site 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20081859 1552406 Ahi1 Abelson helper integration site 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21623382 1552406 Ahi1 Abelson helper integration site 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:23658157 1552406 Ahi1 Abelson helper integration site 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:19718039 1552406 Ahi1 Abelson helper integration site 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19718039 1552406 Ahi1 Abelson helper integration site 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19718039 1552406 Ahi1 Abelson helper integration site 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:19718039 1552406 Ahi1 Abelson helper integration site 1 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:20956301 1552406 Ahi1 Abelson helper integration site 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19718039 1552406 Ahi1 Abelson helper integration site 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:19718039 1552406 Ahi1 Abelson helper integration site 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:19718039 1552406 Ahi1 Abelson helper integration site 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:23658157 1552406 Ahi1 Abelson helper integration site 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:19718039 1552406 Ahi1 Abelson helper integration site 1 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19718039 1552406 Ahi1 Abelson helper integration site 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20081859 1552406 Ahi1 Abelson helper integration site 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:19718039 1552406 Ahi1 Abelson helper integration site 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:19718039 1552406 Ahi1 Abelson helper integration site 1 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:19718039 1552406 Ahi1 Abelson helper integration site 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:19718039 1552406 Ahi1 Abelson helper integration site 1 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20081859 1552406 Ahi1 Abelson helper integration site 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:20081859 1552406 Ahi1 Abelson helper integration site 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:23658157 1552406 Ahi1 Abelson helper integration site 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20081859 1552406 Ahi1 Abelson helper integration site 1 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:20081859 1552406 Ahi1 Abelson helper integration site 1 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:21623382 1552406 Ahi1 Abelson helper integration site 1 gene MP:0009959 abnormal cerebellar hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:21623382 1552406 Ahi1 Abelson helper integration site 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20081859 1552406 Ahi1 Abelson helper integration site 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21623382 1552406 Ahi1 Abelson helper integration site 1 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:19625297 1552406 Ahi1 Abelson helper integration site 1 gene MP:0013305 isosthenuria IAGP N RGD:5509061 20141120 MGI PMID:19718039 1552408 Eomes eomesodermin gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18635804 1552408 Eomes eomesodermin gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:18794345 1552408 Eomes eomesodermin gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:18794345 1552408 Eomes eomesodermin gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:18794345 1552408 Eomes eomesodermin gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18077589 1552408 Eomes eomesodermin gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:18794345 1552408 Eomes eomesodermin gene MP:0001357 increased aggression towards humans IAGP N RGD:5509061 20141003 MGI PMID:18794345 1552408 Eomes eomesodermin gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20220421 MGI PMID:18794345 1552408 Eomes eomesodermin gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10716450 1552408 Eomes eomesodermin gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:19830823 1552408 Eomes eomesodermin gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0001714 absent trophoblast giant cells IAGP N RGD:5509061 20141003 MGI PMID:15788452 1552408 Eomes eomesodermin gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:15788452 1552408 Eomes eomesodermin gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10716450 1552408 Eomes eomesodermin gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15788452 1552408 Eomes eomesodermin gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:18635804 1552408 Eomes eomesodermin gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20713880 1552408 Eomes eomesodermin gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18077589 1552408 Eomes eomesodermin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23897762 1552408 Eomes eomesodermin gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:19830823 1552408 Eomes eomesodermin gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18635804 1552408 Eomes eomesodermin gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:18794345 1552408 Eomes eomesodermin gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:18794345 1552408 Eomes eomesodermin gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:10716450 1552408 Eomes eomesodermin gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:20713880 1552408 Eomes eomesodermin gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18794345 1552408 Eomes eomesodermin gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:19830823 1552408 Eomes eomesodermin gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160421 MGI 1552408 Eomes eomesodermin gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:18794345 1552408 Eomes eomesodermin gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10716450 1552408 Eomes eomesodermin gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1552408 Eomes eomesodermin gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:18794345 1552408 Eomes eomesodermin gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:18077589 1552408 Eomes eomesodermin gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18635804 1552408 Eomes eomesodermin gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:16273099 1552408 Eomes eomesodermin gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:16273099 1552408 Eomes eomesodermin gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16273099 1552408 Eomes eomesodermin gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18635804 1552408 Eomes eomesodermin gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:20713880 1552408 Eomes eomesodermin gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20151231 MGI PMID:24516120 1552408 Eomes eomesodermin gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18077589 1552408 Eomes eomesodermin gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20713880 1552408 Eomes eomesodermin gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18635804 1552408 Eomes eomesodermin gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20713880 1552408 Eomes eomesodermin gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18635804 1552408 Eomes eomesodermin gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:18794345 1552408 Eomes eomesodermin gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:18077589 1552408 Eomes eomesodermin gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16273099 1552408 Eomes eomesodermin gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20713880 1552408 Eomes eomesodermin gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:20713880 1552408 Eomes eomesodermin gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20713880 1552408 Eomes eomesodermin gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:18635804 1552408 Eomes eomesodermin gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:10716450 1552408 Eomes eomesodermin gene MP:0009850 embryonic lethality between implantation and placentation IAGP N RGD:5509061 20141003 MGI PMID:23897762 1552408 Eomes eomesodermin gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20160421 MGI 1552408 Eomes eomesodermin gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:18794345 1552408 Eomes eomesodermin gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1552408 Eomes eomesodermin gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15788452 1552408 Eomes eomesodermin gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19830823 1552408 Eomes eomesodermin gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10716450 1552408 Eomes eomesodermin gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552408 Eomes eomesodermin gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0012102 absent trophectoderm IAGP N RGD:5509061 20141003 MGI PMID:15788452 1552408 Eomes eomesodermin gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0012156 rostral-caudal axis duplication IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0012181 increased somite number IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0012675 enlarged floor plate IAGP N RGD:5509061 20141003 MGI PMID:18171685 1552408 Eomes eomesodermin gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:10716450 1552408 Eomes eomesodermin gene MP:0012739 abnormal anterior primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:10716450 1552408 Eomes eomesodermin gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1552408 Eomes eomesodermin gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1552408 Eomes eomesodermin gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:18635804 1552408 Eomes eomesodermin gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:18077589 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16081683 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15039466 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:16081683 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:16081683 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:16081683 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15039466 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11489994 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15039466 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15039466 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15039466 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16081683 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:17360466 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:17360466 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11086056 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:16081683 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:16081683 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11489994 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15039466 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:17360466 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15039466 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:16081683 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16081683 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0008879 submandibular gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:16081683 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:17360466 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16081683 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11086056 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15039466 1552409 Il12rb2 interleukin 12 receptor, beta 2 gene MP:0013367 parotid gland inflammation IAGP N RGD:5509061 20141225 MGI PMID:16081683 1552410 Gcnt2 glucosaminyl (N-acetyl) transferase 2 (I blood group) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16107727 1552410 Gcnt2 glucosaminyl (N-acetyl) transferase 2 (I blood group) gene MP:0002015 epithelioid cyst IAGP N RGD:5509061 20141003 MGI PMID:16107727 1552410 Gcnt2 glucosaminyl (N-acetyl) transferase 2 (I blood group) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16107727 1552410 Gcnt2 glucosaminyl (N-acetyl) transferase 2 (I blood group) gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16107727 1552410 Gcnt2 glucosaminyl (N-acetyl) transferase 2 (I blood group) gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16107727 1552410 Gcnt2 glucosaminyl (N-acetyl) transferase 2 (I blood group) gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16107727 1552411 Rpusd2 RNA pseudouridylate synthase domain containing 2 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1552411 Rpusd2 RNA pseudouridylate synthase domain containing 2 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20201022 MGI 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:10581033 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:21305608 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000064 failure of bone resorption IAGP N RGD:5509061 20141003 MGI PMID:3976544 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:10581033 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:10581033 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:3998439 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20151112 MGI PMID:25811986 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:10581033 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21305608 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:3976544 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:3998439 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20151112 MGI PMID:25811986 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:10581033 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:10581033 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:3976544 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20151112 MGI PMID:25811986 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:3998439 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:10581033 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000576 clubfoot IEA N RGD:5509061 20111116 MGI 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:3998439 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10581033 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:3998439 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:3998439 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10709991 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19549681 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:3998439 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10709991 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:3998439 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:10581033 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:21305608 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10581033 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19549681 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19549681 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0002360 abnormal spleen B cell corona morphology IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:19549681 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17046993 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20151112 MGI PMID:25811986 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0003053 delayed tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:10709991 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0003053 delayed tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:3998439 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17046993 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0003116 rickets IAGP N RGD:5509061 20151112 MGI PMID:25811986 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:3976544 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:21305608 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:3998439 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:21305608 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:3998439 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:3976544 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:3998439 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:3998439 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0008271 abnormal bone ossification IEA N RGD:5509061 20111116 MGI 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0008463 abnormal peripheral lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:21305608 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:21305608 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0010969 absent compact bone IAGP N RGD:5509061 20151112 MGI PMID:25811986 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:3998439 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0012336 decreased vitamin D level IAGP N RGD:5509061 20151112 MGI PMID:25811986 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0014348 decreased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:15294947 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0030543 abnormal predentin morphology IAGP N RGD:5509061 20180215 MGI PMID:3998439 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:10581033 1552412 Tcirg1 T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:19549681 1552413 Pde8b phosphodiesterase 8B gene MP:0002664 decreased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:21187369 1552413 Pde8b phosphodiesterase 8B gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21187369 1552413 Pde8b phosphodiesterase 8B gene MP:0011549 increased urine corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:21187369 1552414 Mx1 MX dynamin-like GTPase 1 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:17426143 1552414 Mx1 MX dynamin-like GTPase 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160804 MGI 1552414 Mx1 MX dynamin-like GTPase 1 gene MP:0008244 abnormal peritoneal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:7884909 1552414 Mx1 MX dynamin-like GTPase 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:7884909 1552414 Mx1 MX dynamin-like GTPase 1 gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:7769712 1552414 Mx1 MX dynamin-like GTPase 1 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:7884909 1552414 Mx1 MX dynamin-like GTPase 1 gene MP:0020947 decreased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:7769712 1552414 Mx1 MX dynamin-like GTPase 1 gene MP:0020947 decreased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:7884909 1552414 Mx1 MX dynamin-like GTPase 1 gene MP:0031023 decreased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:7769712 1552414 Mx1 MX dynamin-like GTPase 1 gene MP:0031045 decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:7769712 1552414 Mx1 MX dynamin-like GTPase 1 gene MP:0031045 decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:7884909 1552414 Mx1 MX dynamin-like GTPase 1 gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:7884909 1552415 Sgtb small glutamine-rich tetratricopeptide repeat (TPR)-containing, beta gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1552418 Krt15 keratin 15 gene MP:0000466 esophageal epithelium hyperplasia IAGP N RGD:5509061 20180315 MGI PMID:28481227 1552418 Krt15 keratin 15 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20180315 MGI PMID:28481227 1552418 Krt15 keratin 15 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20180315 MGI PMID:28481227 1552419 Map2k6 mitogen-activated protein kinase kinase 6 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:12151339 1552419 Map2k6 mitogen-activated protein kinase kinase 6 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12824301 1552419 Map2k6 mitogen-activated protein kinase kinase 6 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:12824301 1552419 Map2k6 mitogen-activated protein kinase kinase 6 gene MP:0009258 abnormal thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12151339 1552420 Arid4b AT-rich interaction domain 4B gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20200402 MGI 1552420 Arid4b AT-rich interaction domain 4B gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0001147 small testis IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1552420 Arid4b AT-rich interaction domain 4B gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 1552420 Arid4b AT-rich interaction domain 4B gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0001925 male infertility IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20221215 MGI 1552420 Arid4b AT-rich interaction domain 4B gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0003121 genetic imprinting IAGP N RGD:5509061 20141003 MGI PMID:17043311 1552420 Arid4b AT-rich interaction domain 4B gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:17043311 1552420 Arid4b AT-rich interaction domain 4B gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:17043311 1552420 Arid4b AT-rich interaction domain 4B gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200402 MGI 1552420 Arid4b AT-rich interaction domain 4B gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0004924 abnormal behavior IEA N RGD:5509061 20240627 MGI 1552420 Arid4b AT-rich interaction domain 4B gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0004930 small epididymis IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0005159 azoospermia IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18728284 1552420 Arid4b AT-rich interaction domain 4B gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:17043311 1552420 Arid4b AT-rich interaction domain 4B gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:17043311 1552420 Arid4b AT-rich interaction domain 4B gene MP:0009257 dilated seminiferous tubule IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200402 MGI 1552420 Arid4b AT-rich interaction domain 4B gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17043311 1552420 Arid4b AT-rich interaction domain 4B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17043311 1552420 Arid4b AT-rich interaction domain 4B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552420 Arid4b AT-rich interaction domain 4B gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20170803 MGI PMID:26258622 1552420 Arid4b AT-rich interaction domain 4B gene MP:0031070 hemophagocytosis IAGP N RGD:5509061 20200618 MGI PMID:18728284 1552421 Rab35 RAB35, member RAS oncogene family gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20200310 MGI 1552421 Rab35 RAB35, member RAS oncogene family gene MP:0001304 cataract IEA N RGD:5509061 20200310 MGI 1552421 Rab35 RAB35, member RAS oncogene family gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552421 Rab35 RAB35, member RAS oncogene family gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20201029 MGI PMID:32503983 1552421 Rab35 RAB35, member RAS oncogene family gene MP:0012674 tomacula IAGP N RGD:5509061 20201029 MGI PMID:32503983 1552421 Rab35 RAB35, member RAS oncogene family gene MP:0020434 increased astrocyte size IAGP N RGD:5509061 20201029 MGI PMID:32503983 1552422 Cfap20dc CFAP20 domain containing gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20240523 MGI 1552422 Cfap20dc CFAP20 domain containing gene MP:0002834 decreased heart weight IEA N RGD:5509061 20240523 MGI 1552424 Btrc beta-transducin repeat containing protein gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 1552424 Btrc beta-transducin repeat containing protein gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12843402 1552424 Btrc beta-transducin repeat containing protein gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24469832 1552424 Btrc beta-transducin repeat containing protein gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24469832 1552424 Btrc beta-transducin repeat containing protein gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:24469832 1552424 Btrc beta-transducin repeat containing protein gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:24469832 1552424 Btrc beta-transducin repeat containing protein gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20150702 MGI PMID:24469832 1552424 Btrc beta-transducin repeat containing protein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12791266 1552424 Btrc beta-transducin repeat containing protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24469832 1552424 Btrc beta-transducin repeat containing protein gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1552424 Btrc beta-transducin repeat containing protein gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12843402 1552424 Btrc beta-transducin repeat containing protein gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12791266 1552424 Btrc beta-transducin repeat containing protein gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1552424 Btrc beta-transducin repeat containing protein gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:24469832 1552424 Btrc beta-transducin repeat containing protein gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:12843402 1552424 Btrc beta-transducin repeat containing protein gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:12791266 1552424 Btrc beta-transducin repeat containing protein gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:24469832 1552424 Btrc beta-transducin repeat containing protein gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:24469832 1552424 Btrc beta-transducin repeat containing protein gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:24469832 1552424 Btrc beta-transducin repeat containing protein gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12791266 1552424 Btrc beta-transducin repeat containing protein gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:24469832 1552424 Btrc beta-transducin repeat containing protein gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:24469832 1552424 Btrc beta-transducin repeat containing protein gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:12791266 1552424 Btrc beta-transducin repeat containing protein gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:24469832 1552424 Btrc beta-transducin repeat containing protein gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:12791266 1552424 Btrc beta-transducin repeat containing protein gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20150212 MGI PMID:12843402 1552424 Btrc beta-transducin repeat containing protein gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:12843402 1552424 Btrc beta-transducin repeat containing protein gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:12791266 1552424 Btrc beta-transducin repeat containing protein gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:24469832 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20181227 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210520 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20181227 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:7891151 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:7891151 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:3678603 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:3678603 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:20041218 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210520 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20041218 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20041218 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20041218 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210520 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20210128 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20181227 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20201022 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:20041218 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20220811 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20181227 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210520 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0013022 increased Ly6C high monocyte number IEA N RGD:5509061 20181227 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0013025 increased Ly6C low monocyte number IEA N RGD:5509061 20181227 MGI 1552425 Herc1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1552429 Cept1 choline/ethanolaminephosphotransferase 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20180322 MGI PMID:26512026 1552429 Cept1 choline/ethanolaminephosphotransferase 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20180322 MGI PMID:26512026 1552429 Cept1 choline/ethanolaminephosphotransferase 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20180322 MGI PMID:26512026 1552429 Cept1 choline/ethanolaminephosphotransferase 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180322 MGI PMID:26512026 1552429 Cept1 choline/ethanolaminephosphotransferase 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180322 MGI PMID:26512026 1552429 Cept1 choline/ethanolaminephosphotransferase 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20180322 MGI PMID:26512026 1552429 Cept1 choline/ethanolaminephosphotransferase 1 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20180322 MGI PMID:26512026 1552429 Cept1 choline/ethanolaminephosphotransferase 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20180322 MGI PMID:26512026 1552430 Clock clock circadian regulator gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:19629164 1552430 Clock clock circadian regulator gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16879220 1552430 Clock clock circadian regulator gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12882315 1552430 Clock clock circadian regulator gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15967985 1552430 Clock clock circadian regulator gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16732766 1552430 Clock clock circadian regulator gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:15967985 1552430 Clock clock circadian regulator gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:12882315 1552430 Clock clock circadian regulator gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16732766 1552430 Clock clock circadian regulator gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:11050136 1552430 Clock clock circadian regulator gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:11388430 1552430 Clock clock circadian regulator gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16879220 1552430 Clock clock circadian regulator gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16879220 1552430 Clock clock circadian regulator gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:20562852 1552430 Clock clock circadian regulator gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:19387090 1552430 Clock clock circadian regulator gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15523558 1552430 Clock clock circadian regulator gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16879220 1552430 Clock clock circadian regulator gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15523558 1552430 Clock clock circadian regulator gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1552430 Clock clock circadian regulator gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21123577 1552430 Clock clock circadian regulator gene MP:0002311 abnormal inspiratory capacity IEA N RGD:5509061 20240627 MGI 1552430 Clock clock circadian regulator gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12882315 1552430 Clock clock circadian regulator gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:15967985 1552430 Clock clock circadian regulator gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:16732766 1552430 Clock clock circadian regulator gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:20562852 1552430 Clock clock circadian regulator gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16879220 1552430 Clock clock circadian regulator gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:15296754 1552430 Clock clock circadian regulator gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15523558 1552430 Clock clock circadian regulator gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20562852 1552430 Clock clock circadian regulator gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20141003 MGI PMID:15296754 1552430 Clock clock circadian regulator gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20562852 1552430 Clock clock circadian regulator gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:15967985 1552430 Clock clock circadian regulator gene MP:0003969 abnormal luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:15296754 1552430 Clock clock circadian regulator gene MP:0004080 abnormal nucleus accumbens morphology IAGP N RGD:5509061 20141003 MGI PMID:21123577 1552430 Clock clock circadian regulator gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:12882315 1552430 Clock clock circadian regulator gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:18413500 1552430 Clock clock circadian regulator gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16879220 1552430 Clock clock circadian regulator gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:15296754 1552430 Clock clock circadian regulator gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:15296754 1552430 Clock clock circadian regulator gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:15296754 1552430 Clock clock circadian regulator gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:15296754 1552430 Clock clock circadian regulator gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:20562852 1552430 Clock clock circadian regulator gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20562852 1552430 Clock clock circadian regulator gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:20562852 1552430 Clock clock circadian regulator gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17360665 1552430 Clock clock circadian regulator gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:19387090 1552430 Clock clock circadian regulator gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:18413500 1552430 Clock clock circadian regulator gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16879220 1552430 Clock clock circadian regulator gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16879220 1552430 Clock clock circadian regulator gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:16879220 1552430 Clock clock circadian regulator gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21123577 1552430 Clock clock circadian regulator gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20141003 MGI PMID:19629164 1552430 Clock clock circadian regulator gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15296754 1552430 Clock clock circadian regulator gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18007188 1552430 Clock clock circadian regulator gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19387090 1552430 Clock clock circadian regulator gene MP:0008961 abnormal basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:15296754 1552430 Clock clock circadian regulator gene MP:0009015 short proestrus IAGP N RGD:5509061 20141003 MGI PMID:15296754 1552430 Clock clock circadian regulator gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20141003 MGI PMID:15296754 1552430 Clock clock circadian regulator gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:20562852 1552430 Clock clock circadian regulator gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:15296754 1552430 Clock clock circadian regulator gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:15967985 1552430 Clock clock circadian regulator gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0010896 decreased lung compliance IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11388430 1552430 Clock clock circadian regulator gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20171012 MGI PMID:16732766 1552430 Clock clock circadian regulator gene MP:0011021 abnormal circadian regulation of heart rate IAGP N RGD:5509061 20141003 MGI PMID:17360665 1552430 Clock clock circadian regulator gene MP:0011022 abnormal circadian regulation of systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17360665 1552430 Clock clock circadian regulator gene MP:0011044 increased lung elastance IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0013758 increased intestinal glucose absorption IAGP N RGD:5509061 20191031 MGI PMID:19387090 1552430 Clock clock circadian regulator gene MP:0013763 increased T-helper cell number IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0013771 decreased effector memory T-helper cell number IEA N RGD:5509061 20230601 MGI 1552430 Clock clock circadian regulator gene MP:0014121 increased pancreatic islet cell apoptosis IAGP N RGD:5509061 20160324 MGI PMID:20562852 1552430 Clock clock circadian regulator gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:11050136 1552430 Clock clock circadian regulator gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:11388430 1552430 Clock clock circadian regulator gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:16732766 1552430 Clock clock circadian regulator gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:17445238 1552430 Clock clock circadian regulator gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:9160756 1552430 Clock clock circadian regulator gene MP:0020468 abnormal circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:23580255 1552430 Clock clock circadian regulator gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:23580255 1552430 Clock clock circadian regulator gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:8171325 1552430 Clock clock circadian regulator gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:9160756 1552430 Clock clock circadian regulator gene MP:0020471 abnormal circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:8171325 1552430 Clock clock circadian regulator gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:8171325 1552430 Clock clock circadian regulator gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:15967985 1552430 Clock clock circadian regulator gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:16675400 1552430 Clock clock circadian regulator gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:17445238 1552430 Clock clock circadian regulator gene MP:0020474 advanced circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:16675400 1552430 Clock clock circadian regulator gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20171012 MGI PMID:15845877 1552430 Clock clock circadian regulator gene MP:0020478 abnormal circadian sleep/wake cycle IAGP N RGD:5509061 20171012 MGI PMID:11050136 1552430 Clock clock circadian regulator gene MP:0020478 abnormal circadian sleep/wake cycle IAGP N RGD:5509061 20171012 MGI PMID:11388430 1552430 Clock clock circadian regulator gene MP:0020478 abnormal circadian sleep/wake cycle IAGP N RGD:5509061 20171012 MGI PMID:16732766 1552430 Clock clock circadian regulator gene MP:0021198 abnormal sleep duration IAGP N RGD:5509061 20220922 MGI PMID:11050136 1552430 Clock clock circadian regulator gene MP:0021198 abnormal sleep duration IAGP N RGD:5509061 20220922 MGI PMID:11388430 1552430 Clock clock circadian regulator gene MP:0030973 impaired gluconeogenesis IAGP N RGD:5509061 20200102 MGI PMID:15523558 1552432 Ppp4r3a protein phosphatase 4 regulatory subunit 3A gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20220721 MGI PMID:35314861 1552432 Ppp4r3a protein phosphatase 4 regulatory subunit 3A gene MP:0002573 behavioral despair IAGP N RGD:5509061 20220721 MGI PMID:35314861 1552432 Ppp4r3a protein phosphatase 4 regulatory subunit 3A gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20220721 MGI PMID:35314861 1552432 Ppp4r3a protein phosphatase 4 regulatory subunit 3A gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20220721 MGI PMID:35314861 1552432 Ppp4r3a protein phosphatase 4 regulatory subunit 3A gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20220721 MGI PMID:35314861 1552432 Ppp4r3a protein phosphatase 4 regulatory subunit 3A gene MP:0020379 abnormal sucrose solution preference IAGP N RGD:5509061 20220721 MGI PMID:35314861 1552432 Ppp4r3a protein phosphatase 4 regulatory subunit 3A gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20220721 MGI PMID:35314861 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20211021 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0010040 abnormal oval cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552435 Entpd5 ectonucleoside triphosphate diphosphohydrolase 5 gene MP:0010042 abnormal oval cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19176496 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16606670 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0001790 abnormal immune system physiology IEA N RGD:5509061 20111116 MGI 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16606670 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:12847135 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16358363 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15897272 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:15897272 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:16606670 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16606670 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:16606670 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:16358363 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15897272 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15897272 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16606670 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16606670 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17182110 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16606670 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:15897272 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16358363 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16606670 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:16606670 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:16606670 1552436 Pdcd1lg2 programmed cell death 1 ligand 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15897272 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20191107 MGI PMID:29237777 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20191107 MGI PMID:29237777 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230119 MGI 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20191107 MGI PMID:29237777 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20191107 MGI PMID:29237777 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230119 MGI 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20191107 MGI PMID:29237777 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20191107 MGI PMID:29237777 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0009709 hydrometra IEA N RGD:5509061 20230119 MGI 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230119 MGI 1552437 Ccl28 C-C motif chemokine ligand 28 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20191107 MGI PMID:29237777 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0000692 small spleen IAGP N RGD:5509061 20200310 MGI PMID:9294146 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:9294146 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0000706 small thymus IAGP N RGD:5509061 20200310 MGI PMID:9294146 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20200310 MGI PMID:10716994 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:9294146 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:9294146 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:9294146 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:9294146 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20200310 MGI PMID:9294146 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20200310 MGI PMID:9294146 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:10716994 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20200310 MGI PMID:10716994 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20200310 MGI PMID:9294146 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20200310 MGI 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20200310 MGI 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20200310 MGI PMID:10716994 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:10716994 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:9294146 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20200310 MGI PMID:9294146 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0008213 absent immature B cells IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20200310 MGI PMID:9294146 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200310 MGI PMID:9390689 1552438 Xrcc6 X-ray repair complementing defective repair in Chinese hamster cells 6 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20200310 MGI PMID:9294146 1552440 Spef1 sperm flagellar 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1552441 Selenbp1 selenium binding protein 1 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20210520 MGI 1552441 Selenbp1 selenium binding protein 1 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20210520 MGI 1552441 Selenbp1 selenium binding protein 1 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:23500078 1552441 Selenbp1 selenium binding protein 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220519 MGI 1552441 Selenbp1 selenium binding protein 1 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:23500078 1552441 Selenbp1 selenium binding protein 1 gene MP:0002965 increased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:23500078 1552441 Selenbp1 selenium binding protein 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1552441 Selenbp1 selenium binding protein 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23500078 1552441 Selenbp1 selenium binding protein 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23500078 1552441 Selenbp1 selenium binding protein 1 gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:23500078 1552441 Selenbp1 selenium binding protein 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1552441 Selenbp1 selenium binding protein 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1552441 Selenbp1 selenium binding protein 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180222 MGI PMID:29255262 1552441 Selenbp1 selenium binding protein 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220519 MGI 1552441 Selenbp1 selenium binding protein 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20180222 MGI PMID:29255262 1552442 Bola1 bolA family member 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220519 MGI 1552442 Bola1 bolA family member 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1552442 Bola1 bolA family member 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210826 MGI 1552442 Bola1 bolA family member 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1552442 Bola1 bolA family member 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1552442 Bola1 bolA family member 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1552445 Polr3f polymerase (RNA) III (DNA directed) polypeptide F gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20201022 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20200514 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20221215 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20200514 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20220519 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20221215 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210520 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20221215 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210520 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20200514 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20200514 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210520 MGI 1552449 Gnl1 guanine nucleotide binding protein-like 1 gene MP:0010511 shortened PR interval IEA N RGD:5509061 20210520 MGI 1552451 Scin scinderin gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20160428 MGI PMID:25681458 1552451 Scin scinderin gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1552451 Scin scinderin gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20160428 MGI PMID:25681458 1552451 Scin scinderin gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20160428 MGI PMID:25681458 1552451 Scin scinderin gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20160428 MGI PMID:25681458 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0003213 decreased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0003439 abnormal glycerol level IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0004156 abnormal QT variability IEA N RGD:5509061 20220519 MGI 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0010052 increased grip strength IEA N RGD:5509061 20181227 MGI 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0011117 abnormal susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:21803289 1552454 Slc13a5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:21803289 1552455 Fas Fas cell surface death receptor gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:1416659 1552455 Fas Fas cell surface death receptor gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:2708160 1552455 Fas Fas cell surface death receptor gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:8793508 1552455 Fas Fas cell surface death receptor gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8700897 1552455 Fas Fas cell surface death receptor gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:16527894 1552455 Fas Fas cell surface death receptor gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18677469 1552455 Fas Fas cell surface death receptor gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18677469 1552455 Fas Fas cell surface death receptor gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:18677469 1552455 Fas Fas cell surface death receptor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:9036998 1552455 Fas Fas cell surface death receptor gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:18677469 1552455 Fas Fas cell surface death receptor gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:12787314 1552455 Fas Fas cell surface death receptor gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:17608689 1552455 Fas Fas cell surface death receptor gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17509906 1552455 Fas Fas cell surface death receptor gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16118350 1552455 Fas Fas cell surface death receptor gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7581453 1552455 Fas Fas cell surface death receptor gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:10878371 1552455 Fas Fas cell surface death receptor gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:16118350 1552455 Fas Fas cell surface death receptor gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:7628400 1552455 Fas Fas cell surface death receptor gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7581453 1552455 Fas Fas cell surface death receptor gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17509906 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11737079 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11801636 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12787314 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16339515 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16818796 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17509906 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17608689 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18492657 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19528538 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23997217 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:2406366 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7581453 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:8671629 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:8700897 1552455 Fas Fas cell surface death receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0000701 abnormal lymph node size IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0000701 abnormal lymph node size IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11035071 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12787314 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16339515 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16365433 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16818796 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17608689 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18492657 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:2302830 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23997217 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:2406366 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:6975351 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7540652 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7581453 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:762500 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8671629 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8700897 1552455 Fas Fas cell surface death receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:12787314 1552455 Fas Fas cell surface death receptor gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552455 Fas Fas cell surface death receptor gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12787313 1552455 Fas Fas cell surface death receptor gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:12787313 1552455 Fas Fas cell surface death receptor gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:12787313 1552455 Fas Fas cell surface death receptor gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:12787313 1552455 Fas Fas cell surface death receptor gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:12787313 1552455 Fas Fas cell surface death receptor gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:9736651 1552455 Fas Fas cell surface death receptor gene MP:0001017 abnormal stellate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12787313 1552455 Fas Fas cell surface death receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12787313 1552455 Fas Fas cell surface death receptor gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:16541466 1552455 Fas Fas cell surface death receptor gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:16541466 1552455 Fas Fas cell surface death receptor gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:17608689 1552455 Fas Fas cell surface death receptor gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:9036998 1552455 Fas Fas cell surface death receptor gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:18677469 1552455 Fas Fas cell surface death receptor gene MP:0001220 epidermal necrosis IAGP N RGD:5509061 20141003 MGI PMID:16541466 1552455 Fas Fas cell surface death receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12787314 1552455 Fas Fas cell surface death receptor gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18677469 1552455 Fas Fas cell surface death receptor gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:18677469 1552455 Fas Fas cell surface death receptor gene MP:0001346 abnormal lacrimal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17898284 1552455 Fas Fas cell surface death receptor gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12787313 1552455 Fas Fas cell surface death receptor gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12787314 1552455 Fas Fas cell surface death receptor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12787313 1552455 Fas Fas cell surface death receptor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:8496852 1552455 Fas Fas cell surface death receptor gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:8496852 1552455 Fas Fas cell surface death receptor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15192051 1552455 Fas Fas cell surface death receptor gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:16118350 1552455 Fas Fas cell surface death receptor gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:16301622 1552455 Fas Fas cell surface death receptor gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:18677469 1552455 Fas Fas cell surface death receptor gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:9036998 1552455 Fas Fas cell surface death receptor gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:11801636 1552455 Fas Fas cell surface death receptor gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:16365433 1552455 Fas Fas cell surface death receptor gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:11035071 1552455 Fas Fas cell surface death receptor gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11035071 1552455 Fas Fas cell surface death receptor gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:9036998 1552455 Fas Fas cell surface death receptor gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:9236188 1552455 Fas Fas cell surface death receptor gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11035071 1552455 Fas Fas cell surface death receptor gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16818796 1552455 Fas Fas cell surface death receptor gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9236188 1552455 Fas Fas cell surface death receptor gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:15192051 1552455 Fas Fas cell surface death receptor gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0001830 decreased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:18492657 1552455 Fas Fas cell surface death receptor gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:16818796 1552455 Fas Fas cell surface death receptor gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:17574818 1552455 Fas Fas cell surface death receptor gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:2302830 1552455 Fas Fas cell surface death receptor gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:2406366 1552455 Fas Fas cell surface death receptor gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:2708160 1552455 Fas Fas cell surface death receptor gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:9736651 1552455 Fas Fas cell surface death receptor gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:17208228 1552455 Fas Fas cell surface death receptor gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:11737079 1552455 Fas Fas cell surface death receptor gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:12097414 1552455 Fas Fas cell surface death receptor gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552455 Fas Fas cell surface death receptor gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:16339515 1552455 Fas Fas cell surface death receptor gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:9472669 1552455 Fas Fas cell surface death receptor gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11714837 1552455 Fas Fas cell surface death receptor gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15289505 1552455 Fas Fas cell surface death receptor gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:16339515 1552455 Fas Fas cell surface death receptor gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12097414 1552455 Fas Fas cell surface death receptor gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:16339515 1552455 Fas Fas cell surface death receptor gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0001863 blood vessel inflammation IAGP N RGD:5509061 20141003 MGI PMID:18492657 1552455 Fas Fas cell surface death receptor gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20141003 MGI PMID:12571859 1552455 Fas Fas cell surface death receptor gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20141003 MGI PMID:16365433 1552455 Fas Fas cell surface death receptor gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:1565490 1552455 Fas Fas cell surface death receptor gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:16339515 1552455 Fas Fas cell surface death receptor gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:8163351 1552455 Fas Fas cell surface death receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12787313 1552455 Fas Fas cell surface death receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12787313 1552455 Fas Fas cell surface death receptor gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12787314 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12097414 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12571859 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16541466 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16818796 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17574818 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17608689 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18492657 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:2406366 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:6975351 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7540652 1552455 Fas Fas cell surface death receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7581453 1552455 Fas Fas cell surface death receptor gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11801636 1552455 Fas Fas cell surface death receptor gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17898284 1552455 Fas Fas cell surface death receptor gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:9036998 1552455 Fas Fas cell surface death receptor gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:9472669 1552455 Fas Fas cell surface death receptor gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:2406366 1552455 Fas Fas cell surface death receptor gene MP:0002148 abnormal hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:2302830 1552455 Fas Fas cell surface death receptor gene MP:0002148 abnormal hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:2406366 1552455 Fas Fas cell surface death receptor gene MP:0002148 abnormal hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:7581453 1552455 Fas Fas cell surface death receptor gene MP:0002148 abnormal hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:8700897 1552455 Fas Fas cell surface death receptor gene MP:0002163 abnormal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8163351 1552455 Fas Fas cell surface death receptor gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20150108 MGI 1552455 Fas Fas cell surface death receptor gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:12787313 1552455 Fas Fas cell surface death receptor gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:17608689 1552455 Fas Fas cell surface death receptor gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0002221 abnormal lymph organ size IAGP N RGD:5509061 20141003 MGI PMID:2406366 1552455 Fas Fas cell surface death receptor gene MP:0002221 abnormal lymph organ size IAGP N RGD:5509061 20141003 MGI PMID:7581453 1552455 Fas Fas cell surface death receptor gene MP:0002224 abnormal spleen size IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0002334 abnormal airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:11590380 1552455 Fas Fas cell surface death receptor gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:17509906 1552455 Fas Fas cell surface death receptor gene MP:0002375 abnormal thymus medulla morphology IEA N RGD:5509061 20111116 MGI 1552455 Fas Fas cell surface death receptor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15980239 1552455 Fas Fas cell surface death receptor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9820556 1552455 Fas Fas cell surface death receptor gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18677469 1552455 Fas Fas cell surface death receptor gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16339515 1552455 Fas Fas cell surface death receptor gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:3009614 1552455 Fas Fas cell surface death receptor gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17574818 1552455 Fas Fas cell surface death receptor gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9036998 1552455 Fas Fas cell surface death receptor gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17509906 1552455 Fas Fas cell surface death receptor gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17574818 1552455 Fas Fas cell surface death receptor gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17608689 1552455 Fas Fas cell surface death receptor gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:18325838 1552455 Fas Fas cell surface death receptor gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:2406366 1552455 Fas Fas cell surface death receptor gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:6444324 1552455 Fas Fas cell surface death receptor gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:8671629 1552455 Fas Fas cell surface death receptor gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11035071 1552455 Fas Fas cell surface death receptor gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9236188 1552455 Fas Fas cell surface death receptor gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12571859 1552455 Fas Fas cell surface death receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16365433 1552455 Fas Fas cell surface death receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16818796 1552455 Fas Fas cell surface death receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:17509906 1552455 Fas Fas cell surface death receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:2302830 1552455 Fas Fas cell surface death receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:2406366 1552455 Fas Fas cell surface death receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:8700897 1552455 Fas Fas cell surface death receptor gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11737079 1552455 Fas Fas cell surface death receptor gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16365433 1552455 Fas Fas cell surface death receptor gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:17509906 1552455 Fas Fas cell surface death receptor gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:2302830 1552455 Fas Fas cell surface death receptor gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23997217 1552455 Fas Fas cell surface death receptor gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:2406366 1552455 Fas Fas cell surface death receptor gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11737079 1552455 Fas Fas cell surface death receptor gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1552455 Fas Fas cell surface death receptor gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0002533 abnormal type III hypersensitivity reaction IEA N RGD:5509061 20111116 MGI 1552455 Fas Fas cell surface death receptor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12787313 1552455 Fas Fas cell surface death receptor gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:12097414 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:12571859 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16301622 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16365433 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16541466 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16818796 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:17574818 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:18055812 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:18492657 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:9472669 1552455 Fas Fas cell surface death receptor gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552455 Fas Fas cell surface death receptor gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0002936 joint swelling IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11035071 1552455 Fas Fas cell surface death receptor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:12571859 1552455 Fas Fas cell surface death receptor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:16541466 1552455 Fas Fas cell surface death receptor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:16818796 1552455 Fas Fas cell surface death receptor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:23997217 1552455 Fas Fas cell surface death receptor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:9472669 1552455 Fas Fas cell surface death receptor gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20210506 MGI PMID:32547538 1552455 Fas Fas cell surface death receptor gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20111116 MGI 1552455 Fas Fas cell surface death receptor gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16541466 1552455 Fas Fas cell surface death receptor gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11567045 1552455 Fas Fas cell surface death receptor gene MP:0003504 thyroid gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:7628400 1552455 Fas Fas cell surface death receptor gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:12571859 1552455 Fas Fas cell surface death receptor gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:16541466 1552455 Fas Fas cell surface death receptor gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:11971023 1552455 Fas Fas cell surface death receptor gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0003670 dilated renal glomerular capsule IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:11035071 1552455 Fas Fas cell surface death receptor gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:12097414 1552455 Fas Fas cell surface death receptor gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:16818796 1552455 Fas Fas cell surface death receptor gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:18325838 1552455 Fas Fas cell surface death receptor gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:18492657 1552455 Fas Fas cell surface death receptor gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:2302830 1552455 Fas Fas cell surface death receptor gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:8496852 1552455 Fas Fas cell surface death receptor gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:8700897 1552455 Fas Fas cell surface death receptor gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:10607487 1552455 Fas Fas cell surface death receptor gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:9036998 1552455 Fas Fas cell surface death receptor gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20210506 MGI PMID:32547538 1552455 Fas Fas cell surface death receptor gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8163351 1552455 Fas Fas cell surface death receptor gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0003946 renal necrosis IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:10946317 1552455 Fas Fas cell surface death receptor gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0004367 abnormal strial intermediate cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1416659 1552455 Fas Fas cell surface death receptor gene MP:0004368 abnormal stria vascularis vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:8793508 1552455 Fas Fas cell surface death receptor gene MP:0004481 abnormal conjunctival epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17208228 1552455 Fas Fas cell surface death receptor gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:7628400 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11737079 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11801636 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:12486097 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:12571859 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:16365433 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:16541466 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:18325838 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23997217 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:6444324 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:8700897 1552455 Fas Fas cell surface death receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:9036998 1552455 Fas Fas cell surface death receptor gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11737079 1552455 Fas Fas cell surface death receptor gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:8700897 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:11067882 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:11801636 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:16339515 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:16365433 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:16818796 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:17509906 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:17608689 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:18325838 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:18492657 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:23997217 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:2406366 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:6975351 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:8496852 1552455 Fas Fas cell surface death receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:8793508 1552455 Fas Fas cell surface death receptor gene MP:0004795 decreased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0004795 decreased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0004795 decreased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0004797 increased anti-erythrocyte antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0004798 decreased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1552455 Fas Fas cell surface death receptor gene MP:0004798 decreased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:16541466 1552455 Fas Fas cell surface death receptor gene MP:0004798 decreased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0004798 decreased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16237080 1552455 Fas Fas cell surface death receptor gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:17608689 1552455 Fas Fas cell surface death receptor gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:18325838 1552455 Fas Fas cell surface death receptor gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:23997217 1552455 Fas Fas cell surface death receptor gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:8793508 1552455 Fas Fas cell surface death receptor gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:16301622 1552455 Fas Fas cell surface death receptor gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:16339515 1552455 Fas Fas cell surface death receptor gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20210506 MGI PMID:32547538 1552455 Fas Fas cell surface death receptor gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10946317 1552455 Fas Fas cell surface death receptor gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:14530378 1552455 Fas Fas cell surface death receptor gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10946317 1552455 Fas Fas cell surface death receptor gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:12525697 1552455 Fas Fas cell surface death receptor gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:9094710 1552455 Fas Fas cell surface death receptor gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:762500 1552455 Fas Fas cell surface death receptor gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:12571859 1552455 Fas Fas cell surface death receptor gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16365433 1552455 Fas Fas cell surface death receptor gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:2302830 1552455 Fas Fas cell surface death receptor gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:8793508 1552455 Fas Fas cell surface death receptor gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0004955 increased thymus weight IEA N RGD:5509061 20111116 MGI 1552455 Fas Fas cell surface death receptor gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:17608689 1552455 Fas Fas cell surface death receptor gene MP:0005002 abnormal T cell clonal deletion IAGP N RGD:5509061 20141003 MGI PMID:8700897 1552455 Fas Fas cell surface death receptor gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11590380 1552455 Fas Fas cell surface death receptor gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17509906 1552455 Fas Fas cell surface death receptor gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7581453 1552455 Fas Fas cell surface death receptor gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8700897 1552455 Fas Fas cell surface death receptor gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17574818 1552455 Fas Fas cell surface death receptor gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8700897 1552455 Fas Fas cell surface death receptor gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11035071 1552455 Fas Fas cell surface death receptor gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:7540652 1552455 Fas Fas cell surface death receptor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18492657 1552455 Fas Fas cell surface death receptor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23997217 1552455 Fas Fas cell surface death receptor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9075933 1552455 Fas Fas cell surface death receptor gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:12594834 1552455 Fas Fas cell surface death receptor gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:6610701 1552455 Fas Fas cell surface death receptor gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12571859 1552455 Fas Fas cell surface death receptor gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16339515 1552455 Fas Fas cell surface death receptor gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16818796 1552455 Fas Fas cell surface death receptor gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17608689 1552455 Fas Fas cell surface death receptor gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17898284 1552455 Fas Fas cell surface death receptor gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:18492657 1552455 Fas Fas cell surface death receptor gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:23997217 1552455 Fas Fas cell surface death receptor gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:7540652 1552455 Fas Fas cell surface death receptor gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17509906 1552455 Fas Fas cell surface death receptor gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:3009614 1552455 Fas Fas cell surface death receptor gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7581453 1552455 Fas Fas cell surface death receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18325838 1552455 Fas Fas cell surface death receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552455 Fas Fas cell surface death receptor gene MP:0005265 abnormal blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18492657 1552455 Fas Fas cell surface death receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11801636 1552455 Fas Fas cell surface death receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12097414 1552455 Fas Fas cell surface death receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552455 Fas Fas cell surface death receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17574818 1552455 Fas Fas cell surface death receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:9472669 1552455 Fas Fas cell surface death receptor gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8496852 1552455 Fas Fas cell surface death receptor gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18325838 1552455 Fas Fas cell surface death receptor gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:762500 1552455 Fas Fas cell surface death receptor gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:11801636 1552455 Fas Fas cell surface death receptor gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:16301622 1552455 Fas Fas cell surface death receptor gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:6444324 1552455 Fas Fas cell surface death receptor gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1552455 Fas Fas cell surface death receptor gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:12097414 1552455 Fas Fas cell surface death receptor gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16365433 1552455 Fas Fas cell surface death receptor gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:9472669 1552455 Fas Fas cell surface death receptor gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1552455 Fas Fas cell surface death receptor gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20111116 MGI 1552455 Fas Fas cell surface death receptor gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:12974753 1552455 Fas Fas cell surface death receptor gene MP:0005614 decreased susceptibility to type III hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:12571859 1552455 Fas Fas cell surface death receptor gene MP:0005615 increased susceptibility to type III hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:8793508 1552455 Fas Fas cell surface death receptor gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16541466 1552455 Fas Fas cell surface death receptor gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11590380 1552455 Fas Fas cell surface death receptor gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16527894 1552455 Fas Fas cell surface death receptor gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10453074 1552455 Fas Fas cell surface death receptor gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17509906 1552455 Fas Fas cell surface death receptor gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:8496852 1552455 Fas Fas cell surface death receptor gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:9736651 1552455 Fas Fas cell surface death receptor gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:12787313 1552455 Fas Fas cell surface death receptor gene MP:0006315 abnormal urine protein level IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:17574818 1552455 Fas Fas cell surface death receptor gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:3009614 1552455 Fas Fas cell surface death receptor gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:762500 1552455 Fas Fas cell surface death receptor gene MP:0008044 increased NK cell number IEA N RGD:5509061 20150108 MGI 1552455 Fas Fas cell surface death receptor gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21479271 1552455 Fas Fas cell surface death receptor gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16541466 1552455 Fas Fas cell surface death receptor gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17608689 1552455 Fas Fas cell surface death receptor gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17898284 1552455 Fas Fas cell surface death receptor gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16339515 1552455 Fas Fas cell surface death receptor gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18492657 1552455 Fas Fas cell surface death receptor gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18492657 1552455 Fas Fas cell surface death receptor gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:17574818 1552455 Fas Fas cell surface death receptor gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11737079 1552455 Fas Fas cell surface death receptor gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:17509906 1552455 Fas Fas cell surface death receptor gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0008136 enlarged Peyer's patches IEA N RGD:5509061 20111116 MGI 1552455 Fas Fas cell surface death receptor gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0008180 abnormal marginal zone B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12486097 1552455 Fas Fas cell surface death receptor gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0008206 increased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:17608689 1552455 Fas Fas cell surface death receptor gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11035071 1552455 Fas Fas cell surface death receptor gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11971023 1552455 Fas Fas cell surface death receptor gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:7540652 1552455 Fas Fas cell surface death receptor gene MP:0008350 increased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:7540652 1552455 Fas Fas cell surface death receptor gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:17608689 1552455 Fas Fas cell surface death receptor gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1552455 Fas Fas cell surface death receptor gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:18492657 1552455 Fas Fas cell surface death receptor gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:18492657 1552455 Fas Fas cell surface death receptor gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9109438 1552455 Fas Fas cell surface death receptor gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11737079 1552455 Fas Fas cell surface death receptor gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1552455 Fas Fas cell surface death receptor gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:8700897 1552455 Fas Fas cell surface death receptor gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:11737079 1552455 Fas Fas cell surface death receptor gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:23997217 1552455 Fas Fas cell surface death receptor gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:8700897 1552455 Fas Fas cell surface death receptor gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:11737079 1552455 Fas Fas cell surface death receptor gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:8700897 1552455 Fas Fas cell surface death receptor gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11737079 1552455 Fas Fas cell surface death receptor gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:15265950 1552455 Fas Fas cell surface death receptor gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:22773818 1552455 Fas Fas cell surface death receptor gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:8700897 1552455 Fas Fas cell surface death receptor gene MP:0008542 enlarged cervical lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11801636 1552455 Fas Fas cell surface death receptor gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16301622 1552455 Fas Fas cell surface death receptor gene MP:0008573 increased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1552455 Fas Fas cell surface death receptor gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0008626 increased circulating interleukin-5 level IAGP N RGD:5509061 20141003 MGI PMID:16301622 1552455 Fas Fas cell surface death receptor gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:6610701 1552455 Fas Fas cell surface death receptor gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:6975351 1552455 Fas Fas cell surface death receptor gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:17898284 1552455 Fas Fas cell surface death receptor gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552455 Fas Fas cell surface death receptor gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:3009614 1552455 Fas Fas cell surface death receptor gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552455 Fas Fas cell surface death receptor gene MP:0008766 abnormal B cell receptor editing IAGP N RGD:5509061 20141003 MGI PMID:12486097 1552455 Fas Fas cell surface death receptor gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16973389 1552455 Fas Fas cell surface death receptor gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16118350 1552455 Fas Fas cell surface death receptor gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:6444324 1552455 Fas Fas cell surface death receptor gene MP:0008879 submandibular gland inflammation IAGP N RGD:5509061 20141218 MGI PMID:7957574 1552455 Fas Fas cell surface death receptor gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:1565490 1552455 Fas Fas cell surface death receptor gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:17898284 1552455 Fas Fas cell surface death receptor gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:18055812 1552455 Fas Fas cell surface death receptor gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141204 MGI PMID:8163351 1552455 Fas Fas cell surface death receptor gene MP:0008891 decreased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16118350 1552455 Fas Fas cell surface death receptor gene MP:0008978 abnormal vagina weight IAGP N RGD:5509061 20141003 MGI PMID:10453074 1552455 Fas Fas cell surface death receptor gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9236188 1552455 Fas Fas cell surface death receptor gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9236188 1552455 Fas Fas cell surface death receptor gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9820556 1552455 Fas Fas cell surface death receptor gene MP:0010065 decreased circulating creatine level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0010138 arteritis IAGP N RGD:5509061 20141003 MGI PMID:12571859 1552455 Fas Fas cell surface death receptor gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12097414 1552455 Fas Fas cell surface death receptor gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9834083 1552455 Fas Fas cell surface death receptor gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190328 MGI 1552455 Fas Fas cell surface death receptor gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190328 MGI 1552455 Fas Fas cell surface death receptor gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0010922 alveolitis IAGP N RGD:5509061 20141003 MGI PMID:15148335 1552455 Fas Fas cell surface death receptor gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0011081 decreased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19741297 1552455 Fas Fas cell surface death receptor gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17574818 1552455 Fas Fas cell surface death receptor gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:12097414 1552455 Fas Fas cell surface death receptor gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552455 Fas Fas cell surface death receptor gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:16267157 1552455 Fas Fas cell surface death receptor gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0011369 increased renal glomerulus apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0011402 renal cast IEA N RGD:5509061 20111116 MGI 1552455 Fas Fas cell surface death receptor gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:12097414 1552455 Fas Fas cell surface death receptor gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:12571859 1552455 Fas Fas cell surface death receptor gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12571859 1552455 Fas Fas cell surface death receptor gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18275831 1552455 Fas Fas cell surface death receptor gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0011445 abnormal renal protein reabsorption IAGP N RGD:5509061 20141003 MGI PMID:18779924 1552455 Fas Fas cell surface death receptor gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12571859 1552455 Fas Fas cell surface death receptor gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0011483 renal glomerular synechia IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:12571859 1552455 Fas Fas cell surface death receptor gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:17073941 1552455 Fas Fas cell surface death receptor gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:17142777 1552455 Fas Fas cell surface death receptor gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:17574818 1552455 Fas Fas cell surface death receptor gene MP:0011567 increased renal glomerulus lobularity IAGP N RGD:5509061 20141003 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0011742 decreased urine nitrite level IAGP N RGD:5509061 20141003 MGI PMID:9236188 1552455 Fas Fas cell surface death receptor gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:1416659 1552455 Fas Fas cell surface death receptor gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:2708160 1552455 Fas Fas cell surface death receptor gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:8793508 1552455 Fas Fas cell surface death receptor gene MP:0012433 decreased ovarian tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20505730 1552455 Fas Fas cell surface death receptor gene MP:0013452 increased lacrimal gland apoptosis IAGP N RGD:5509061 20150205 MGI PMID:17898284 1552455 Fas Fas cell surface death receptor gene MP:0013455 lacrimal gland atrophy IAGP N RGD:5509061 20160324 MGI PMID:1565490 1552455 Fas Fas cell surface death receptor gene MP:0013585 thymus cortex atrophy IEA N RGD:5509061 20150319 MGI 1552455 Fas Fas cell surface death receptor gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:11971023 1552455 Fas Fas cell surface death receptor gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:17608689 1552455 Fas Fas cell surface death receptor gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:16541466 1552455 Fas Fas cell surface death receptor gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:16818796 1552455 Fas Fas cell surface death receptor gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:17574818 1552455 Fas Fas cell surface death receptor gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:23616572 1552455 Fas Fas cell surface death receptor gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:9736651 1552455 Fas Fas cell surface death receptor gene MP:0021186 decreased bone mineral density of vertebrae IAGP N RGD:5509061 20220915 MGI PMID:17259598 1552455 Fas Fas cell surface death receptor gene MP:0031051 lymph node hemorrhage IAGP N RGD:5509061 20200618 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0031051 lymph node hemorrhage IAGP N RGD:5509061 20200618 MGI PMID:6609979 1552455 Fas Fas cell surface death receptor gene MP:0031052 lymph node necrosis IAGP N RGD:5509061 20200618 MGI PMID:309911 1552455 Fas Fas cell surface death receptor gene MP:0031052 lymph node necrosis IAGP N RGD:5509061 20200618 MGI PMID:6609979 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18288109 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:17382885 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23805138 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:17382885 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:17382885 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0008206 increased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17676052 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20151112 MGI PMID:19706873 1552456 Bak1 BCL2-antagonist/killer 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11163212 1552458 Rnf146 ring finger protein 146 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:28287403 1552458 Rnf146 ring finger protein 146 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20200310 MGI PMID:28287403 1552458 Rnf146 ring finger protein 146 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20200310 MGI PMID:28287403 1552458 Rnf146 ring finger protein 146 gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20200310 MGI PMID:28287403 1552458 Rnf146 ring finger protein 146 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20200310 MGI PMID:28287403 1552458 Rnf146 ring finger protein 146 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20200310 MGI PMID:28287403 1552458 Rnf146 ring finger protein 146 gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:28287403 1552458 Rnf146 ring finger protein 146 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20200310 MGI PMID:28287403 1552458 Rnf146 ring finger protein 146 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20200310 MGI PMID:28287403 1552458 Rnf146 ring finger protein 146 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0010965 decreased compact bone volume IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0011504 abnormal limb long bone morphology IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20200310 MGI PMID:28287403 1552458 Rnf146 ring finger protein 146 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0030009 increased bone marrow adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0030387 large posterior fontanelle IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0030439 decreased osteoblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0030471 abnormal ameloblast differentiation IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552458 Rnf146 ring finger protein 146 gene MP:0030985 decreased circulating osteocalcin level IAGP N RGD:5509061 20200310 MGI PMID:28581440 1552461 Sdad1 SDA1 domain containing 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20210930 MGI PMID:33905568 1552461 Sdad1 SDA1 domain containing 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 1552462 Fuca2 fucosidase, alpha-L- 2, plasma gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170406 MGI 1552463 Pex5l peroxisomal biogenesis factor 5-like gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:21593326 1552463 Pex5l peroxisomal biogenesis factor 5-like gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:21593326 1552463 Pex5l peroxisomal biogenesis factor 5-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21555075 1552463 Pex5l peroxisomal biogenesis factor 5-like gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:21593326 1552463 Pex5l peroxisomal biogenesis factor 5-like gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:21593326 1552463 Pex5l peroxisomal biogenesis factor 5-like gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21593326 1552464 Tek TEK receptor tyrosine kinase gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:7596437 1552464 Tek TEK receptor tyrosine kinase gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:9683559 1552464 Tek TEK receptor tyrosine kinase gene MP:0000263 absent organized vascular network IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0000264 failure of vascular branching IAGP N RGD:5509061 20141003 MGI PMID:15899871 1552464 Tek TEK receptor tyrosine kinase gene MP:0000264 failure of vascular branching IAGP N RGD:5509061 20141003 MGI PMID:9683559 1552464 Tek TEK receptor tyrosine kinase gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15899871 1552464 Tek TEK receptor tyrosine kinase gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9683559 1552464 Tek TEK receptor tyrosine kinase gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20200514 MGI 1552464 Tek TEK receptor tyrosine kinase gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:7477259 1552464 Tek TEK receptor tyrosine kinase gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:15899871 1552464 Tek TEK receptor tyrosine kinase gene MP:0000296 absent trabeculae carneae IAGP N RGD:5509061 20141003 MGI PMID:9683559 1552464 Tek TEK receptor tyrosine kinase gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:9683559 1552464 Tek TEK receptor tyrosine kinase gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 1552464 Tek TEK receptor tyrosine kinase gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:7477259 1552464 Tek TEK receptor tyrosine kinase gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7477259 1552464 Tek TEK receptor tyrosine kinase gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15899871 1552464 Tek TEK receptor tyrosine kinase gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15899871 1552464 Tek TEK receptor tyrosine kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 1552464 Tek TEK receptor tyrosine kinase gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:7596437 1552464 Tek TEK receptor tyrosine kinase gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15899871 1552464 Tek TEK receptor tyrosine kinase gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:7596437 1552464 Tek TEK receptor tyrosine kinase gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15899871 1552464 Tek TEK receptor tyrosine kinase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7596437 1552464 Tek TEK receptor tyrosine kinase gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15899871 1552464 Tek TEK receptor tyrosine kinase gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:7477259 1552464 Tek TEK receptor tyrosine kinase gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 1552464 Tek TEK receptor tyrosine kinase gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20150212 MGI PMID:25202984 1552464 Tek TEK receptor tyrosine kinase gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15899871 1552464 Tek TEK receptor tyrosine kinase gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9683559 1552464 Tek TEK receptor tyrosine kinase gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0009274 buphthalmos IAGP N RGD:5509061 20150212 MGI PMID:25202984 1552464 Tek TEK receptor tyrosine kinase gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15899871 1552464 Tek TEK receptor tyrosine kinase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7596437 1552464 Tek TEK receptor tyrosine kinase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20150528 MGI PMID:25686605 1552464 Tek TEK receptor tyrosine kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552464 Tek TEK receptor tyrosine kinase gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:10498691 1552464 Tek TEK receptor tyrosine kinase gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:9683559 1552464 Tek TEK receptor tyrosine kinase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1552464 Tek TEK receptor tyrosine kinase gene MP:0031213 increased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:25202984 1552464 Tek TEK receptor tyrosine kinase gene MP:0031500 increased cornea size IAGP N RGD:5509061 20230810 MGI PMID:25202984 1552466 Nit1 nitrilase 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16864578 1552466 Nit1 nitrilase 1 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:16864578 1552466 Nit1 nitrilase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16864578 1552466 Nit1 nitrilase 1 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:16864578 1552466 Nit1 nitrilase 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16864578 1552468 Dld dihydrolipoamide dehydrogenase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9405644 1552468 Dld dihydrolipoamide dehydrogenase gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9405644 1552468 Dld dihydrolipoamide dehydrogenase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9405644 1552468 Dld dihydrolipoamide dehydrogenase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9405644 1552468 Dld dihydrolipoamide dehydrogenase gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9405644 1552470 Kifc1 kinesin family member C1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 1552470 Kifc1 kinesin family member C1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1552471 Abhd10 abhydrolase domain containing 10 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1552471 Abhd10 abhydrolase domain containing 10 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20240523 MGI 1552471 Abhd10 abhydrolase domain containing 10 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20230601 MGI 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14993262 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14993262 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20141003 MGI PMID:16327803 1552474 Dnaja3 DnaJ heat shock protein family (Hsp40) member A3 gene MP:0014390 decreased myocardial fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:16327803 1552475 Serpinb6a serine (or cysteine) peptidase inhibitor, clade B, member 6a gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15082799 1552478 Rrbp1 ribosome binding protein 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210520 MGI 1552478 Rrbp1 ribosome binding protein 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1552478 Rrbp1 ribosome binding protein 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1552478 Rrbp1 ribosome binding protein 1 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20240523 MGI 1552478 Rrbp1 ribosome binding protein 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210520 MGI 1552478 Rrbp1 ribosome binding protein 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1552478 Rrbp1 ribosome binding protein 1 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20240523 MGI 1552478 Rrbp1 ribosome binding protein 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1552478 Rrbp1 ribosome binding protein 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 1552478 Rrbp1 ribosome binding protein 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1552478 Rrbp1 ribosome binding protein 1 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1552478 Rrbp1 ribosome binding protein 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210520 MGI 1552478 Rrbp1 ribosome binding protein 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 1552478 Rrbp1 ribosome binding protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1552483 Tm2d2 TM2 domain containing 2 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20201022 MGI 1552483 Tm2d2 TM2 domain containing 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20221215 MGI 1552483 Tm2d2 TM2 domain containing 2 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1552483 Tm2d2 TM2 domain containing 2 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20201231 MGI 1552483 Tm2d2 TM2 domain containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552484 Bbc3 BCL2 binding component 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18287039 1552484 Bbc3 BCL2 binding component 3 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:14585359 1552484 Bbc3 BCL2 binding component 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20818388 1552484 Bbc3 BCL2 binding component 3 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:18077368 1552484 Bbc3 BCL2 binding component 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18077368 1552484 Bbc3 BCL2 binding component 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18077368 1552484 Bbc3 BCL2 binding component 3 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:18077368 1552484 Bbc3 BCL2 binding component 3 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18048346 1552484 Bbc3 BCL2 binding component 3 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:16399862 1552484 Bbc3 BCL2 binding component 3 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:14500851 1552484 Bbc3 BCL2 binding component 3 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:14585359 1552484 Bbc3 BCL2 binding component 3 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:14585359 1552484 Bbc3 BCL2 binding component 3 gene MP:0003823 increased left ventricle developed pressure IAGP N RGD:5509061 20141003 MGI PMID:16399862 1552484 Bbc3 BCL2 binding component 3 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18287039 1552484 Bbc3 BCL2 binding component 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18032672 1552484 Bbc3 BCL2 binding component 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18077368 1552484 Bbc3 BCL2 binding component 3 gene MP:0005571 decreased lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:16399862 1552484 Bbc3 BCL2 binding component 3 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16399862 1552484 Bbc3 BCL2 binding component 3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18287039 1552484 Bbc3 BCL2 binding component 3 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18287039 1552484 Bbc3 BCL2 binding component 3 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:14500851 1552484 Bbc3 BCL2 binding component 3 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:18077368 1552484 Bbc3 BCL2 binding component 3 gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:16399862 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0000111 cleft palate IAGP N RGD:5509061 20180830 MGI PMID:29208648 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20220519 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220519 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0001148 enlarged testis IEA N RGD:5509061 20220519 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20210826 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20230601 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20220519 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220811 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20220519 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0002639 micrognathia IAGP N RGD:5509061 20180830 MGI PMID:29208648 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0002989 small kidney IEA N RGD:5509061 20220519 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20230601 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1552485 Tgds TDP-glucose 4,6-dehydratase gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1552486 Pdhb pyruvate dehydrogenase (lipoamide) beta gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20201022 MGI 1552486 Pdhb pyruvate dehydrogenase (lipoamide) beta gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1552486 Pdhb pyruvate dehydrogenase (lipoamide) beta gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20201022 MGI 1552486 Pdhb pyruvate dehydrogenase (lipoamide) beta gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20201022 MGI 1552486 Pdhb pyruvate dehydrogenase (lipoamide) beta gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20201022 MGI 1552486 Pdhb pyruvate dehydrogenase (lipoamide) beta gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20201022 MGI 1552486 Pdhb pyruvate dehydrogenase (lipoamide) beta gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1552486 Pdhb pyruvate dehydrogenase (lipoamide) beta gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1552486 Pdhb pyruvate dehydrogenase (lipoamide) beta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1552486 Pdhb pyruvate dehydrogenase (lipoamide) beta gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552486 Pdhb pyruvate dehydrogenase (lipoamide) beta gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1552487 Zfp52 zinc finger protein 52 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20210128 MGI 1552487 Zfp52 zinc finger protein 52 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1552487 Zfp52 zinc finger protein 52 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210520 MGI 1552487 Zfp52 zinc finger protein 52 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1552488 Erlin2 ER lipid raft associated 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20210128 MGI 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:22045334 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20200310 MGI PMID:22045334 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:22552287 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200310 MGI PMID:22045334 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:22552287 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22552287 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:28107482 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22552287 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20200310 MGI PMID:22045334 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0002174 abnormal gastrulation movements IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22552287 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:22045334 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20200310 MGI PMID:22552287 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22552287 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22552287 1552490 Smurf2 SMAD specific E3 ubiquitin protein ligase 2 gene MP:0012675 enlarged floor plate IAGP N RGD:5509061 20200310 MGI PMID:19379695 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:10811868 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:15593118 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10811868 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0005398 decreased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:15593118 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15593118 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:10811868 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:10811868 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:10811868 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:10811868 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10811868 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0010935 increased airway resistance IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552492 Ccr4 C-C motif chemokine receptor 4 gene MP:0010936 decreased airway resistance IAGP N RGD:5509061 20141003 MGI PMID:12154006 1552495 Rffl ring finger and FYVE like domain containing protein gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1552495 Rffl ring finger and FYVE like domain containing protein gene MP:0000277 abnormal heart shape IEA N RGD:5509061 20210128 MGI 1552495 Rffl ring finger and FYVE like domain containing protein gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1552495 Rffl ring finger and FYVE like domain containing protein gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1552495 Rffl ring finger and FYVE like domain containing protein gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1552495 Rffl ring finger and FYVE like domain containing protein gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1552495 Rffl ring finger and FYVE like domain containing protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19138581 1552499 F12 coagulation factor XII (Hageman factor) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15351846 1552499 F12 coagulation factor XII (Hageman factor) gene MP:0003075 abnormal response to CNS ischemic injury IAGP N RGD:5509061 20141003 MGI PMID:16533887 1552499 F12 coagulation factor XII (Hageman factor) gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:16533887 1552499 F12 coagulation factor XII (Hageman factor) gene MP:0009812 abnormal bradykinin level IAGP N RGD:5509061 20170323 MGI PMID:16732380 1552499 F12 coagulation factor XII (Hageman factor) gene MP:0012359 increased partial thromboplastin time IAGP N RGD:5509061 20170323 MGI PMID:16732380 1552505 Sars1 seryl-tRNA synthetase 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20191128 MGI 1552505 Sars1 seryl-tRNA synthetase 1 gene MP:0005102 abnormal iris pigmentation IEA N RGD:5509061 20231207 MGI 1552505 Sars1 seryl-tRNA synthetase 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20240523 MGI 1552505 Sars1 seryl-tRNA synthetase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 1552505 Sars1 seryl-tRNA synthetase 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20191128 MGI 1552505 Sars1 seryl-tRNA synthetase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1552505 Sars1 seryl-tRNA synthetase 1 gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20191128 MGI 1552505 Sars1 seryl-tRNA synthetase 1 gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20191128 MGI 1552505 Sars1 seryl-tRNA synthetase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20231207 MGI 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0000105 impaired ossification of basisphenoid bone IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0000111 cleft palate IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0000440 domed cranium IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210128 MGI 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240627 MGI 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20210520 MGI 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0002639 micrognathia IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20210826 MGI 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0003842 abnormal metopic suture morphology IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004282 retrognathia IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004380 short frontal bone IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004421 enlarged parietal bone IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004454 absent pterygoid process IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004592 small mandible IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0010043 abnormal frontonasal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0011642 abnormal bone collagen fibril morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0012546 triangular face IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0013545 cleft hard palate IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0014012 abnormal cranial blood vasculature morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0020301 short tongue IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0030066 short face IAGP N RGD:5509061 20170921 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0030067 narrow face IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0030069 broad face IAGP N RGD:5509061 20170921 MGI PMID:17986521 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0030316 enlarged neurocranium IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0030431 wide metopic suture IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0030533 abnormal snout skin morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 1552507 Ankrd11 ankyrin repeat domain 11 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:33996804 1552508 Letmd1 LETM1 domain containing 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1552508 Letmd1 LETM1 domain containing 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230601 MGI 1552508 Letmd1 LETM1 domain containing 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20220324 MGI PMID:34910916 1552508 Letmd1 LETM1 domain containing 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 1552508 Letmd1 LETM1 domain containing 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20220324 MGI PMID:34910916 1552508 Letmd1 LETM1 domain containing 1 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20220324 MGI PMID:34910916 1552508 Letmd1 LETM1 domain containing 1 gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20220324 MGI PMID:34910916 1552508 Letmd1 LETM1 domain containing 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20220324 MGI PMID:34910916 1552508 Letmd1 LETM1 domain containing 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20220324 MGI PMID:34910916 1552508 Letmd1 LETM1 domain containing 1 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20220324 MGI PMID:34910916 1552508 Letmd1 LETM1 domain containing 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1552508 Letmd1 LETM1 domain containing 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1552508 Letmd1 LETM1 domain containing 1 gene MP:0011015 decreased body surface temperature IAGP N RGD:5509061 20220324 MGI PMID:34910916 1552508 Letmd1 LETM1 domain containing 1 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20220324 MGI PMID:34910916 1552508 Letmd1 LETM1 domain containing 1 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20220324 MGI PMID:34910916 1552508 Letmd1 LETM1 domain containing 1 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20220324 MGI PMID:34910916 1552508 Letmd1 LETM1 domain containing 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1552508 Letmd1 LETM1 domain containing 1 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20220324 MGI PMID:34910916 1552508 Letmd1 LETM1 domain containing 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 1552508 Letmd1 LETM1 domain containing 1 gene MP:0020426 abnormal beige fat cell physiology IAGP N RGD:5509061 20220324 MGI PMID:34910916 1552508 Letmd1 LETM1 domain containing 1 gene MP:0020520 whitened brown adipose tissue morphology IAGP N RGD:5509061 20220324 MGI PMID:34910916 1552508 Letmd1 LETM1 domain containing 1 gene MP:0020522 decreased susceptibility to xenobiotic induced hyperthermia IAGP N RGD:5509061 20220324 MGI PMID:34910916 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22082675 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20220519 MGI 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0001304 cataract IEA N RGD:5509061 20210826 MGI 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:16505176 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20221215 MGI 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:16505176 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0003068 enlarged kidney IEA N RGD:5509061 20220519 MGI 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16505176 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16505176 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0003547 abnormal pulmonary pressure IAGP N RGD:5509061 20141003 MGI PMID:22082675 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22082675 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0004832 enlarged ovary IEA N RGD:5509061 20220519 MGI 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22082675 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16505176 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0005629 abnormal lung weight IAGP N RGD:5509061 20141003 MGI PMID:16505176 1552509 Nol3 nucleolar protein 3 (apoptosis repressor with CARD domain) gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22082675 1552510 Or51e1 olfactory receptor family 51 subfamily E member 1 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20240404 MGI PMID:38507492 1552510 Or51e1 olfactory receptor family 51 subfamily E member 1 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20240404 MGI PMID:38507492 1552510 Or51e1 olfactory receptor family 51 subfamily E member 1 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20240404 MGI PMID:38507492 1552510 Or51e1 olfactory receptor family 51 subfamily E member 1 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20240404 MGI PMID:38507492 1552510 Or51e1 olfactory receptor family 51 subfamily E member 1 gene MP:0005583 decreased renin activity IAGP N RGD:5509061 20240404 MGI PMID:38507492 1552510 Or51e1 olfactory receptor family 51 subfamily E member 1 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20240404 MGI PMID:38507492 1552510 Or51e1 olfactory receptor family 51 subfamily E member 1 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20240404 MGI PMID:38507492 1552510 Or51e1 olfactory receptor family 51 subfamily E member 1 gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20240404 MGI PMID:38507492 1552510 Or51e1 olfactory receptor family 51 subfamily E member 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20240404 MGI PMID:38507492 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0003066 increased liver copper level IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0003067 decreased liver copper level IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20190808 MGI 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20190808 MGI 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20190808 MGI 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0003952 abnormal copper level IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0005636 abnormal mineral homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20190808 MGI 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0009615 abnormal zinc homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0010248 decreased intestine copper level IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22737083 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17483098 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1552511 Slc39a4 solute carrier family 39 (zinc transporter), member 4 gene MP:0020385 decreased intestinal iron level IAGP N RGD:5509061 20161020 MGI PMID:22737083 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23748901 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:23720746 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:23720746 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23748901 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23748901 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23748901 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23748901 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23748901 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:23748901 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23748901 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:23748901 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23748901 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23720746 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:23748901 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20141003 MGI PMID:23748901 1552512 Atat1 alpha tubulin acetyltransferase 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:23748901 1552513 Prickle2 prickle planar cell polarity protein 2 gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20200310 MGI PMID:21276947 1552513 Prickle2 prickle planar cell polarity protein 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20200310 MGI PMID:21276947 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0000120 malocclusion IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0000160 kyphosis IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0000418 focal hair loss IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0001194 dermatitis IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0001212 skin lesions IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0001958 emphysema IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0002016 ovary cyst IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0002750 exophthalmos IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0005015 increased T cell number IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18343975 1552516 Tom1l2 target of myb1-like 2 (chicken) gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:18343975 1552517 Eri1 exoribonuclease 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:18438418 1552517 Eri1 exoribonuclease 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:18438418 1552517 Eri1 exoribonuclease 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:18438418 1552517 Eri1 exoribonuclease 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200310 MGI PMID:18438418 1552517 Eri1 exoribonuclease 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18438418 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20200310 MGI PMID:28067313 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20200310 MGI PMID:28067313 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20200310 MGI PMID:28067313 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20200310 MGI PMID:28067313 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:23896986 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20200310 MGI PMID:28067313 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20200310 MGI PMID:28067313 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0004357 long tibia IEA N RGD:5509061 20210128 MGI 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20200310 MGI PMID:28067313 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:23896986 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200310 MGI PMID:23896986 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:28067313 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0008823 abnormal interventricular septum membranous part morphology IAGP N RGD:5509061 20200310 MGI PMID:28067313 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28067313 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28067313 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28067313 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:23896986 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0013848 subcutaneous edema IAGP N RGD:5509061 20200310 MGI PMID:28067313 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:28067313 1552518 Baiap2l1 BAI1-associated protein 2-like 1 gene MP:0020102 increased hepatic glucose production IAGP N RGD:5509061 20200310 MGI PMID:23896986 1552524 Enpp5 ectonucleotide pyrophosphatase/phosphodiesterase 5 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1552524 Enpp5 ectonucleotide pyrophosphatase/phosphodiesterase 5 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20201022 MGI 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20200310 MGI PMID:23643363 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0002082 postnatal lethality IEA N RGD:5509061 20200310 MGI 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:23643363 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200310 MGI PMID:23643363 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0004979 abnormal neuronal precursor cell number IAGP N RGD:5509061 20200310 MGI PMID:23643363 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210826 MGI 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20200310 MGI PMID:23643363 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20200310 MGI PMID:23643363 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0008946 abnormal neuron number IAGP N RGD:5509061 20200310 MGI PMID:23643363 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0009430 increased embryo weight IAGP N RGD:5509061 20200310 MGI PMID:23643363 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20200310 MGI PMID:23643363 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210826 MGI 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23643363 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23643363 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1552525 Smarcc2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20201015 MGI PMID:26720614 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:22375002 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:22375002 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0001575 cyanosis IAGP N RGD:5509061 20201015 MGI PMID:26720614 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:22375002 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0001954 respiratory distress IAGP N RGD:5509061 20201015 MGI PMID:26720614 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201015 MGI PMID:26720614 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:21273312 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:21273312 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20200310 MGI PMID:21273312 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20200310 MGI PMID:22375002 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:22375002 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20200310 MGI PMID:22375002 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20200310 MGI PMID:22375002 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20200310 MGI PMID:22375002 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20200310 MGI PMID:22833682 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20200310 MGI PMID:22833682 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:21273312 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20201015 MGI PMID:26720614 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22375002 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21273312 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0014381 abnormal miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:21273312 1552526 Cc2d1a coiled-coil and C2 domain containing 1A gene MP:0014384 increased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:21273312 1552527 Nceh1 neutral cholesterol ester hydrolase 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:19723498 1552527 Nceh1 neutral cholesterol ester hydrolase 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:19723498 1552527 Nceh1 neutral cholesterol ester hydrolase 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:19723498 1552527 Nceh1 neutral cholesterol ester hydrolase 1 gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20200310 MGI PMID:19723498 1552527 Nceh1 neutral cholesterol ester hydrolase 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:19723498 1552527 Nceh1 neutral cholesterol ester hydrolase 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20200310 MGI PMID:19723498 1552527 Nceh1 neutral cholesterol ester hydrolase 1 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20200310 MGI PMID:19723498 1552527 Nceh1 neutral cholesterol ester hydrolase 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:19723498 1552527 Nceh1 neutral cholesterol ester hydrolase 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20200310 MGI PMID:15840715 1552533 Abhd14a abhydrolase domain containing 14A gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1552533 Abhd14a abhydrolase domain containing 14A gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 1552535 Tpmt thiopurine methyltransferase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17510427 1552535 Tpmt thiopurine methyltransferase gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:17510427 1552535 Tpmt thiopurine methyltransferase gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:17510427 1552535 Tpmt thiopurine methyltransferase gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:17510427 1552535 Tpmt thiopurine methyltransferase gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17510427 1552537 Pkmyt1 protein kinase, membrane associated tyrosine/threonine 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20201022 MGI 1552537 Pkmyt1 protein kinase, membrane associated tyrosine/threonine 1 gene MP:0000603 pale liver IEA N RGD:5509061 20210520 MGI 1552537 Pkmyt1 protein kinase, membrane associated tyrosine/threonine 1 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20210520 MGI 1552537 Pkmyt1 protein kinase, membrane associated tyrosine/threonine 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1552537 Pkmyt1 protein kinase, membrane associated tyrosine/threonine 1 gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1552537 Pkmyt1 protein kinase, membrane associated tyrosine/threonine 1 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20210520 MGI 1552537 Pkmyt1 protein kinase, membrane associated tyrosine/threonine 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20200310 MGI 1552537 Pkmyt1 protein kinase, membrane associated tyrosine/threonine 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552537 Pkmyt1 protein kinase, membrane associated tyrosine/threonine 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20210826 MGI 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20220331 MGI PMID:34298397 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20220331 MGI PMID:34221868 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20220331 MGI PMID:34221868 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20200310 MGI 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20220331 MGI PMID:34221868 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20200310 MGI 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20200310 MGI 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:28874825 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20220331 MGI PMID:34221868 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20200310 MGI PMID:28874825 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20220331 MGI PMID:34221868 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20220331 MGI PMID:34221868 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20220331 MGI PMID:34221868 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20220331 MGI PMID:34221868 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20220331 MGI PMID:34221868 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200310 MGI 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20220331 MGI PMID:34221868 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0011637 abnormal mitochondrial matrix morphology IAGP N RGD:5509061 20220331 MGI PMID:34221868 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0013299 decreased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20220331 MGI PMID:34298397 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20220331 MGI PMID:34221868 1552540 Atp5if1 ATP synthase inhibitory factor subunit 1 gene MP:0014234 decreased enterocyte apoptosis IAGP N RGD:5509061 20230323 MGI PMID:34221868 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:9367982 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:9859212 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:9859212 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:9859212 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17141159 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9367982 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9859212 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9859212 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:9367982 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9367982 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20160310 MGI PMID:24905170 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9367982 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:17141159 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:9859212 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9367982 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9859212 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9367982 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19592277 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19592277 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:19592277 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:17141159 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0003279 aneurysm IAGP N RGD:5509061 20141003 MGI PMID:9367982 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:17141159 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9859212 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:17141159 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0004879 decreased systemic vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:17141159 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20190307 MGI PMID:27027284 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19592277 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:17141159 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9367982 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9367982 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:17141159 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19592277 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19592277 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19592277 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9859212 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:9367982 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20160310 MGI PMID:24905170 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9367982 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9859212 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17141159 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:17141159 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0013026 decreased Ly6C low monocyte number IAGP N RGD:5509061 20170413 MGI PMID:27814941 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:9367982 1552542 Klf2 Kruppel-like transcription factor 2 (lung) gene MP:0031589 detached epicardium IAGP N RGD:5509061 20240229 MGI PMID:17141159 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20220519 MGI 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20211021 MGI 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20240627 MGI PMID:38011999 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20240627 MGI PMID:38011999 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0008526 decreased cranium width IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0010031 abnormal cranium size IAGP N RGD:5509061 20141003 MGI PMID:22234171 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552543 Eif4h eukaryotic translation initiation factor 4H gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:21465509 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20200310 MGI PMID:23835334 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:21465509 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200310 MGI PMID:20023287 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:21465509 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:21465509 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0003221 abnormal cardiomyocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0003948 abnormal gas homeostasis IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:23835334 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:20023287 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200310 MGI PMID:20023287 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0006087 increased body mass index IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20200310 MGI PMID:20023287 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0009119 increased brown fat cell size IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:20023287 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:21465509 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0012236 abnormal cholangiocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:21465509 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0012270 cardiac edema IAGP N RGD:5509061 20200310 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20200310 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20200310 MGI PMID:21465509 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20200310 MGI PMID:21465509 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20200310 MGI PMID:21641555 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21465509 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21465509 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:23835334 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0031418 increased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:16675698 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0031418 increased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:21857651 1552545 Pnpla2 patatin-like phospholipase domain containing 2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:16675698 1552548 Tm9sf2 transmembrane 9 superfamily member 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1552548 Tm9sf2 transmembrane 9 superfamily member 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20220519 MGI 1552548 Tm9sf2 transmembrane 9 superfamily member 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20220519 MGI 1552548 Tm9sf2 transmembrane 9 superfamily member 2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220519 MGI 1552548 Tm9sf2 transmembrane 9 superfamily member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1552548 Tm9sf2 transmembrane 9 superfamily member 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1552550 Parp9 poly (ADP-ribose) polymerase family, member 9 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20210805 MGI PMID:33976210 1552550 Parp9 poly (ADP-ribose) polymerase family, member 9 gene MP:0008548 abnormal circulating interferon level IAGP N RGD:5509061 20210805 MGI PMID:33976210 1552550 Parp9 poly (ADP-ribose) polymerase family, member 9 gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20210805 MGI PMID:33976210 1552552 Hdac7 histone deacetylase 7 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:16873063 1552552 Hdac7 histone deacetylase 7 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:16873063 1552552 Hdac7 histone deacetylase 7 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16873063 1552552 Hdac7 histone deacetylase 7 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16873063 1552552 Hdac7 histone deacetylase 7 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210826 MGI 1552552 Hdac7 histone deacetylase 7 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:16873063 1552552 Hdac7 histone deacetylase 7 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16873063 1552552 Hdac7 histone deacetylase 7 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 1552552 Hdac7 histone deacetylase 7 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:16873063 1552552 Hdac7 histone deacetylase 7 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:16873063 1552552 Hdac7 histone deacetylase 7 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:16873063 1552552 Hdac7 histone deacetylase 7 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16873063 1552552 Hdac7 histone deacetylase 7 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20210826 MGI 1552552 Hdac7 histone deacetylase 7 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16873063 1552552 Hdac7 histone deacetylase 7 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16873063 1552552 Hdac7 histone deacetylase 7 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16873063 1552552 Hdac7 histone deacetylase 7 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16873063 1552552 Hdac7 histone deacetylase 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16873063 1552552 Hdac7 histone deacetylase 7 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20240523 MGI 1552554 Memo1 mediator of cell motility 1 gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20160811 MGI 1552554 Memo1 mediator of cell motility 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0000653 abnormal sex gland morphology IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1552554 Memo1 mediator of cell motility 1 gene MP:0001512 trunk curl IEA N RGD:5509061 20201231 MGI 1552554 Memo1 mediator of cell motility 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1552554 Memo1 mediator of cell motility 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1552554 Memo1 mediator of cell motility 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20211021 MGI 1552554 Memo1 mediator of cell motility 1 gene MP:0004450 presphenoid bone hypoplasia IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0004461 basisphenoid bone hypoplasia IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0008275 failure of endochondral bone ossification IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0009892 palate bone hypoplasia IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0009896 palatine bone horizontal plate hypoplasia IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0009898 maxillary shelf hypoplasia IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0012337 increased vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:24056085 1552554 Memo1 mediator of cell motility 1 gene MP:0013807 generalized edema IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0030027 basioccipital bone hypoplasia IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0030033 abnormal nasal bridge morphology IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0030351 wide coronal suture IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0030431 wide metopic suture IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552554 Memo1 mediator of cell motility 1 gene MP:0030467 abnormal cranial cartilage development IAGP N RGD:5509061 20230504 MGI PMID:26746790 1552555 Lgmn legumain gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1552555 Lgmn legumain gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12775715 1552555 Lgmn legumain gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:19879164 1552555 Lgmn legumain gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1552555 Lgmn legumain gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0005060 accumulation of giant lysosomes in kidney/renal tubule cells IAGP N RGD:5509061 20141003 MGI PMID:12775715 1552555 Lgmn legumain gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:12775715 1552555 Lgmn legumain gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19879164 1552555 Lgmn legumain gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:19879164 1552555 Lgmn legumain gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:19879164 1552555 Lgmn legumain gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1552555 Lgmn legumain gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19106291 1552555 Lgmn legumain gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0011379 abnormal kidney outer medulla outer stripe morphology IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0011425 abnormal kidney interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552555 Lgmn legumain gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:21292981 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:16645591 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17347480 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17251423 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19705551 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17251423 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:18341994 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0001756 abnormal urination IAGP N RGD:5509061 20141003 MGI PMID:12161756 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:19794112 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:10764638 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:15128844 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:23263443 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19244541 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0001987 alcohol preference IAGP N RGD:5509061 20141003 MGI PMID:19705551 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10821274 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16327782 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16943565 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:15509739 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:16943565 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19794112 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20141003 MGI PMID:10821274 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:17553498 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:10764638 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:10821274 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20141003 MGI PMID:19705551 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:18341994 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:19794112 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0003022 increased coronary flow rate IAGP N RGD:5509061 20141003 MGI PMID:16314376 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:10764638 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:23263443 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:19705551 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0003821 decreased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:16314376 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0003823 increased left ventricle developed pressure IAGP N RGD:5509061 20141003 MGI PMID:16314376 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20141003 MGI PMID:15763167 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:16314376 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:19155296 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20151217 MGI PMID:24462040 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20240530 MGI PMID:33358893 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17251423 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:15266010 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:19794112 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19794112 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:15509739 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:18503767 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:10764638 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19794112 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:19794112 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:19794112 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:15763167 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18503767 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20141003 MGI PMID:16645591 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0008860 abnormal hair cycle telogen phase IAGP N RGD:5509061 20141003 MGI PMID:16645591 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15121805 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15128844 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17553498 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18341994 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:16327782 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:18503767 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0009287 decreased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18503767 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17251423 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17251423 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19794112 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:19705551 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0010055 abnormal sensory neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:10764638 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0010055 abnormal sensory neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18499726 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0010072 increased pruritus IAGP N RGD:5509061 20141003 MGI PMID:23263443 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0010073 decreased pruritus IAGP N RGD:5509061 20240530 MGI PMID:33358893 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:16943565 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20180125 MGI PMID:18503767 1552559 Trpv1 transient receptor potential cation channel, subfamily V, member 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:18503767 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0000160 kyphosis IEA N RGD:5509061 20111116 MGI 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:4596202 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20171109 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:4596202 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:4596202 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20141003 MGI 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20171109 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20141003 MGI 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20171109 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0001156 abnormal spermatogenesis IEA N RGD:5509061 20111116 MGI 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:4596202 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20240718 MGI PMID:34237032 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0001577 anemia IEA N RGD:5509061 20111116 MGI 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20171109 MGI PMID:6831040 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:4596202 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20627074 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:4596202 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20240718 MGI PMID:34237032 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0002209 decreased germ cell number IEA N RGD:5509061 20111116 MGI 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:4596202 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20141003 MGI 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:4596202 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:4596202 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20171109 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20171109 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:20627074 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0003950 abnormal plasma membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:20627074 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20171109 MGI PMID:6466874 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20627074 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20171109 MGI PMID:6466874 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0005114 premature hair loss IEA N RGD:5509061 20111116 MGI 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0005431 decreased oocyte number IEA N RGD:5509061 20111222 MGI 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20141003 MGI 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20627074 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20240718 MGI PMID:34237032 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20141003 MGI PMID:4596202 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20171109 MGI PMID:16219534 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:20627074 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20240718 MGI PMID:34237032 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0009859 eye opacity IEA N RGD:5509061 20150326 MGI 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160804 MGI 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20240718 MGI PMID:34237032 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:20460369 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0012010 parturition failure IAGP N RGD:5509061 20191219 MGI PMID:1756209 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0013539 increased ovary adenoma incidence IEA N RGD:5509061 20150326 MGI 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20240718 MGI PMID:34237032 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0030942 abnormal microtubule organizing center morphology IAGP N RGD:5509061 20190718 MGI PMID:20627074 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:20627074 1552560 Cdk5rap2 CDK5 regulatory subunit associated protein 2 gene MP:0030944 abnormal pericentriolar material morphology IAGP N RGD:5509061 20190718 MGI PMID:20627074 1552564 Lyl1 lymphoblastomic leukemia 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16514064 1552564 Lyl1 lymphoblastomic leukemia 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16514064 1552564 Lyl1 lymphoblastomic leukemia 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21387538 1552564 Lyl1 lymphoblastomic leukemia 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16514064 1552564 Lyl1 lymphoblastomic leukemia 1 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16514064 1552564 Lyl1 lymphoblastomic leukemia 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21387538 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0002059 abnormal seminal vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0002990 short ureter IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0003586 dilated ureter IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0003942 abnormal urinary system development IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0004017 duplex kidney IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0004967 abnormal kidney epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0009085 abnormal uterine horn morphology IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0010980 ectopic ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0011493 double ureter IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0011803 double kidney pelvis IAGP N RGD:5509061 20141003 MGI PMID:21949185 1552566 Lzts2 leucine zipper, putative tumor suppressor 2 gene MP:0013320 dilated seminal vesicle IAGP N RGD:5509061 20141204 MGI PMID:21949185 1552569 Veph1 ventricular zone expressed PH domain-containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15388229 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:23274954 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:12405636 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:8510385 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:23274954 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:8510385 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23274954 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23274954 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23274954 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8510385 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:23274954 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:12405636 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:23274954 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:8510385 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17928412 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:8510385 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141030 MGI PMID:24700869 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:12405636 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0004875 increased mean systemic arterial blood pressure IEA N RGD:5509061 20190103 MGI 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:8510385 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0006143 increased systemic arterial diastolic blood pressure IEA N RGD:5509061 20190103 MGI 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0006144 increased systemic arterial systolic blood pressure IEA N RGD:5509061 20190103 MGI 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:12405636 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141030 MGI PMID:24700869 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20190103 MGI 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:23274954 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23274954 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0010422 heart right ventricle hypoplasia IEA N RGD:5509061 20141003 MGI 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0010845 decreased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0010851 decreased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0011249 abdominal situs inversus IAGP N RGD:5509061 20141003 MGI PMID:23274954 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0011252 situs inversus totalis IAGP N RGD:5509061 20141003 MGI PMID:23274954 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20141003 MGI PMID:12405636 1552572 Nek8 NIMA (never in mitosis gene a)-related expressed kinase 8 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:23274954 1552573 Pax3 paired box 3 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:18832392 1552573 Pax3 paired box 3 gene MP:0000088 short mandible IAGP N RGD:5509061 20221020 MGI PMID:32692983 1552573 Pax3 paired box 3 gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20230309 MGI PMID:23872235 1552573 Pax3 paired box 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230309 MGI PMID:23872235 1552573 Pax3 paired box 3 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0000154 rib fusion IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231102 MGI PMID:35899771 1552573 Pax3 paired box 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15132998 1552573 Pax3 paired box 3 gene MP:0000371 diluted coat color IEA N RGD:5509061 20111116 MGI 1552573 Pax3 paired box 3 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:11857794 1552573 Pax3 paired box 3 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:14170406 1552573 Pax3 paired box 3 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:15384171 1552573 Pax3 paired box 3 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:16951257 1552573 Pax3 paired box 3 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:20045680 1552573 Pax3 paired box 3 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:20095975 1552573 Pax3 paired box 3 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:21512107 1552573 Pax3 paired box 3 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:21867959 1552573 Pax3 paired box 3 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:9344762 1552573 Pax3 paired box 3 gene MP:0000373 belly spot IAGP N RGD:5509061 20160616 MGI PMID:26952979 1552573 Pax3 paired box 3 gene MP:0000373 belly spot IAGP N RGD:5509061 20170824 MGI PMID:28043919 1552573 Pax3 paired box 3 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:18832392 1552573 Pax3 paired box 3 gene MP:0000445 short snout IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0000585 kinked tail IEA N RGD:5509061 20111116 MGI 1552573 Pax3 paired box 3 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:15132998 1552573 Pax3 paired box 3 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:16951257 1552573 Pax3 paired box 3 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:17360543 1552573 Pax3 paired box 3 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:7600971 1552573 Pax3 paired box 3 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:8631247 1552573 Pax3 paired box 3 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:15132998 1552573 Pax3 paired box 3 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:21512107 1552573 Pax3 paired box 3 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:23785297 1552573 Pax3 paired box 3 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20231109 MGI PMID:36400788 1552573 Pax3 paired box 3 gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:15843801 1552573 Pax3 paired box 3 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:21512107 1552573 Pax3 paired box 3 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23785297 1552573 Pax3 paired box 3 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 1552573 Pax3 paired box 3 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20150528 MGI PMID:7976186 1552573 Pax3 paired box 3 gene MP:0000822 abnormal brain ventricle morphology IEA N RGD:5509061 20111116 MGI 1552573 Pax3 paired box 3 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:7976186 1552573 Pax3 paired box 3 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15384171 1552573 Pax3 paired box 3 gene MP:0000898 midbrain hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10699180 1552573 Pax3 paired box 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17492753 1552573 Pax3 paired box 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20045680 1552573 Pax3 paired box 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20095975 1552573 Pax3 paired box 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21512107 1552573 Pax3 paired box 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21867959 1552573 Pax3 paired box 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:2763211 1552573 Pax3 paired box 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:7976186 1552573 Pax3 paired box 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9344762 1552573 Pax3 paired box 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20230309 MGI PMID:23872235 1552573 Pax3 paired box 3 gene MP:0000919 cranioschisis IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:7976186 1552573 Pax3 paired box 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10699180 1552573 Pax3 paired box 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11914272 1552573 Pax3 paired box 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:12358782 1552573 Pax3 paired box 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17492753 1552573 Pax3 paired box 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21512107 1552573 Pax3 paired box 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21867959 1552573 Pax3 paired box 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:4826095 1552573 Pax3 paired box 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:5912439 1552573 Pax3 paired box 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:9344762 1552573 Pax3 paired box 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20170824 MGI PMID:28043919 1552573 Pax3 paired box 3 gene MP:0000936 small embryonic telencephalon IEA N RGD:5509061 20111116 MGI 1552573 Pax3 paired box 3 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0000959 abnormal somatic sensory system morphology IAGP N RGD:5509061 20141003 MGI PMID:16906226 1552573 Pax3 paired box 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17492753 1552573 Pax3 paired box 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21512107 1552573 Pax3 paired box 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:2763211 1552573 Pax3 paired box 3 gene MP:0000962 disorganized dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:2763211 1552573 Pax3 paired box 3 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20160616 MGI PMID:26952979 1552573 Pax3 paired box 3 gene MP:0001061 abnormal oculomotor nerve morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0001063 abnormal trochlear nerve morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:17492753 1552573 Pax3 paired box 3 gene MP:0001177 atelectasis IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0001189 absent skin pigmentation IEA N RGD:5509061 20111116 MGI 1552573 Pax3 paired box 3 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18330927 1552573 Pax3 paired box 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21539826 1552573 Pax3 paired box 3 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20230309 MGI PMID:23872235 1552573 Pax3 paired box 3 gene MP:0001341 absent eyelids IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:17360543 1552573 Pax3 paired box 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:18330927 1552573 Pax3 paired box 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:20045680 1552573 Pax3 paired box 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16720875 1552573 Pax3 paired box 3 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:21512107 1552573 Pax3 paired box 3 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:8661050 1552573 Pax3 paired box 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170824 MGI PMID:28043919 1552573 Pax3 paired box 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17492753 1552573 Pax3 paired box 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17360543 1552573 Pax3 paired box 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:20045680 1552573 Pax3 paired box 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:21539826 1552573 Pax3 paired box 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:23622066 1552573 Pax3 paired box 3 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15489287 1552573 Pax3 paired box 3 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15384171 1552573 Pax3 paired box 3 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20160616 MGI PMID:26952979 1552573 Pax3 paired box 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:18330927 1552573 Pax3 paired box 3 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:21867959 1552573 Pax3 paired box 3 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20111116 MGI 1552573 Pax3 paired box 3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10699180 1552573 Pax3 paired box 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15729346 1552573 Pax3 paired box 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18198335 1552573 Pax3 paired box 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20095975 1552573 Pax3 paired box 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21512107 1552573 Pax3 paired box 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23650549 1552573 Pax3 paired box 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:2763211 1552573 Pax3 paired box 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:473084 1552573 Pax3 paired box 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11857794 1552573 Pax3 paired box 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15489287 1552573 Pax3 paired box 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20045680 1552573 Pax3 paired box 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23650549 1552573 Pax3 paired box 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:17360543 1552573 Pax3 paired box 3 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20160623 MGI PMID:25807280 1552573 Pax3 paired box 3 gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17360543 1552573 Pax3 paired box 3 gene MP:0002367 abnormal thymus lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:5912439 1552573 Pax3 paired box 3 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:24121508 1552573 Pax3 paired box 3 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:15384171 1552573 Pax3 paired box 3 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:20045680 1552573 Pax3 paired box 3 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:9344762 1552573 Pax3 paired box 3 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:23622066 1552573 Pax3 paired box 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:9344762 1552573 Pax3 paired box 3 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:9344762 1552573 Pax3 paired box 3 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:24121508 1552573 Pax3 paired box 3 gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:24121508 1552573 Pax3 paired box 3 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:20095975 1552573 Pax3 paired box 3 gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:21867959 1552573 Pax3 paired box 3 gene MP:0002939 head spot IAGP N RGD:5509061 20141003 MGI PMID:11857794 1552573 Pax3 paired box 3 gene MP:0002939 head spot IAGP N RGD:5509061 20141003 MGI PMID:14170406 1552573 Pax3 paired box 3 gene MP:0002940 variable body spotting IEA N RGD:5509061 20111116 MGI 1552573 Pax3 paired box 3 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:15132998 1552573 Pax3 paired box 3 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:15384171 1552573 Pax3 paired box 3 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:21512107 1552573 Pax3 paired box 3 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:24121508 1552573 Pax3 paired box 3 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20150326 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:21867959 1552573 Pax3 paired box 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:2763211 1552573 Pax3 paired box 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20170824 MGI PMID:28043919 1552573 Pax3 paired box 3 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:10699180 1552573 Pax3 paired box 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:15132998 1552573 Pax3 paired box 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:16712836 1552573 Pax3 paired box 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:16951257 1552573 Pax3 paired box 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:20045680 1552573 Pax3 paired box 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:20095975 1552573 Pax3 paired box 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:21512107 1552573 Pax3 paired box 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:21867959 1552573 Pax3 paired box 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:2763211 1552573 Pax3 paired box 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:6665745 1552573 Pax3 paired box 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20170824 MGI PMID:28043919 1552573 Pax3 paired box 3 gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:15132998 1552573 Pax3 paired box 3 gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:21512107 1552573 Pax3 paired box 3 gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:8631247 1552573 Pax3 paired box 3 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:5912439 1552573 Pax3 paired box 3 gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20141003 MGI PMID:18198335 1552573 Pax3 paired box 3 gene MP:0003247 abnormal glutaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18198335 1552573 Pax3 paired box 3 gene MP:0003248 loss of glutamate neurons IAGP N RGD:5509061 20141003 MGI PMID:18198335 1552573 Pax3 paired box 3 gene MP:0003359 hypaxial muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0003359 hypaxial muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17360543 1552573 Pax3 paired box 3 gene MP:0003359 hypaxial muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0003359 hypaxial muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20045680 1552573 Pax3 paired box 3 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20150528 MGI PMID:7976186 1552573 Pax3 paired box 3 gene MP:0003717 pallor IAGP N RGD:5509061 20221020 MGI PMID:32692983 1552573 Pax3 paired box 3 gene MP:0003760 decreased palatal length IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0003792 abnormal major salivary gland morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 1552573 Pax3 paired box 3 gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:17360543 1552573 Pax3 paired box 3 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:4826095 1552573 Pax3 paired box 3 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:21354128 1552573 Pax3 paired box 3 gene MP:0003939 abnormal myotome morphology IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:21354128 1552573 Pax3 paired box 3 gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20141003 MGI PMID:16951257 1552573 Pax3 paired box 3 gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20141003 MGI PMID:21512107 1552573 Pax3 paired box 3 gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20141003 MGI PMID:8631247 1552573 Pax3 paired box 3 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:9344762 1552573 Pax3 paired box 3 gene MP:0004248 abnormal epaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17360543 1552573 Pax3 paired box 3 gene MP:0004289 abnormal bony labyrinth IAGP N RGD:5509061 20141003 MGI PMID:5912439 1552573 Pax3 paired box 3 gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20230309 MGI PMID:23872235 1552573 Pax3 paired box 3 gene MP:0004383 absent interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0004419 absent parietal bone IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0004419 absent parietal bone IAGP N RGD:5509061 20230309 MGI PMID:23872235 1552573 Pax3 paired box 3 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0004454 absent pterygoid process IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0004458 absent alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0004460 alisphenoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0004477 turbinate hypoplasia IAGP N RGD:5509061 20170921 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0004592 small mandible IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0004612 fusion of vertebral bodies IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0004760 increased mitotic index IEA N RGD:5509061 20111116 MGI 1552573 Pax3 paired box 3 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0004838 abnormal neural fold elevation formation IAGP N RGD:5509061 20141003 MGI PMID:9344762 1552573 Pax3 paired box 3 gene MP:0004846 absent skeletal muscle IAGP N RGD:5509061 20141003 MGI PMID:21512107 1552573 Pax3 paired box 3 gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0004914 absent ultimobranchial body IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:24121508 1552573 Pax3 paired box 3 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:18198335 1552573 Pax3 paired box 3 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20230309 MGI PMID:23872235 1552573 Pax3 paired box 3 gene MP:0005171 absent coat pigmentation IEA N RGD:5509061 20111116 MGI 1552573 Pax3 paired box 3 gene MP:0005314 absent thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:21867959 1552573 Pax3 paired box 3 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:18330927 1552573 Pax3 paired box 3 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:5912439 1552573 Pax3 paired box 3 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20221020 MGI PMID:32692983 1552573 Pax3 paired box 3 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:5912439 1552573 Pax3 paired box 3 gene MP:0006062 abnormal vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:5912439 1552573 Pax3 paired box 3 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:5912439 1552573 Pax3 paired box 3 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:20045680 1552573 Pax3 paired box 3 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231102 MGI PMID:35899771 1552573 Pax3 paired box 3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0006284 absent hypaxial muscle IAGP N RGD:5509061 20141003 MGI PMID:20045680 1552573 Pax3 paired box 3 gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0008065 short endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:5912439 1552573 Pax3 paired box 3 gene MP:0008237 abnormal ventral coat pigmentation IAGP N RGD:5509061 20170824 MGI PMID:28043919 1552573 Pax3 paired box 3 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0008301 adrenal medulla hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16906226 1552573 Pax3 paired box 3 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0008460 absent dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0008460 absent dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:15132998 1552573 Pax3 paired box 3 gene MP:0008460 absent dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:21512107 1552573 Pax3 paired box 3 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:23622066 1552573 Pax3 paired box 3 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20170824 MGI PMID:28043919 1552573 Pax3 paired box 3 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20150528 MGI PMID:7976186 1552573 Pax3 paired box 3 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23622066 1552573 Pax3 paired box 3 gene MP:0009245 caudal rachischisis IAGP N RGD:5509061 20141003 MGI PMID:14170406 1552573 Pax3 paired box 3 gene MP:0009247 meteorism IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141225 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0009407 increased skeletal muscle fiber density IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20221020 MGI PMID:32692983 1552573 Pax3 paired box 3 gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20141225 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:20045680 1552573 Pax3 paired box 3 gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:24121508 1552573 Pax3 paired box 3 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221020 MGI PMID:32692983 1552573 Pax3 paired box 3 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0009909 bifid tongue IAGP N RGD:5509061 20221020 MGI PMID:32692983 1552573 Pax3 paired box 3 gene MP:0009933 abnormal tail hair pigmentation IAGP N RGD:5509061 20160616 MGI PMID:26952979 1552573 Pax3 paired box 3 gene MP:0009933 abnormal tail hair pigmentation IAGP N RGD:5509061 20170824 MGI PMID:28043919 1552573 Pax3 paired box 3 gene MP:0009934 abnormal hind foot hair pigmentation IAGP N RGD:5509061 20170824 MGI PMID:28043919 1552573 Pax3 paired box 3 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18198335 1552573 Pax3 paired box 3 gene MP:0010016 variable depigmentation IAGP N RGD:5509061 20141003 MGI PMID:15132998 1552573 Pax3 paired box 3 gene MP:0010056 ectopic skeletal muscle IAGP N RGD:5509061 20141003 MGI PMID:23785297 1552573 Pax3 paired box 3 gene MP:0010073 decreased pruritus IAGP N RGD:5509061 20141003 MGI PMID:23622066 1552573 Pax3 paired box 3 gene MP:0010231 transverse fur striping IAGP N RGD:5509061 20170824 MGI PMID:28043919 1552573 Pax3 paired box 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9344762 1552573 Pax3 paired box 3 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0010457 pulmonary artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:18330927 1552573 Pax3 paired box 3 gene MP:0010459 supravalvar pulmonary trunk stenosis IAGP N RGD:5509061 20141003 MGI PMID:18330927 1552573 Pax3 paired box 3 gene MP:0010463 aorta stenosis IAGP N RGD:5509061 20141003 MGI PMID:18330927 1552573 Pax3 paired box 3 gene MP:0010572 persistent right dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20231102 MGI PMID:35899771 1552573 Pax3 paired box 3 gene MP:0010589 common truncal valve IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0010628 patent tricuspid valve IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0010649 dilated pulmonary trunk IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21539826 1552573 Pax3 paired box 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18330927 1552573 Pax3 paired box 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16906226 1552573 Pax3 paired box 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17360543 1552573 Pax3 paired box 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20045680 1552573 Pax3 paired box 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:32692983 1552573 Pax3 paired box 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14170406 1552573 Pax3 paired box 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15132998 1552573 Pax3 paired box 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16951257 1552573 Pax3 paired box 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21354128 1552573 Pax3 paired box 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21539826 1552573 Pax3 paired box 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15843801 1552573 Pax3 paired box 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20045680 1552573 Pax3 paired box 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20095975 1552573 Pax3 paired box 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20160512 MGI PMID:14170406 1552573 Pax3 paired box 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23410975 1552573 Pax3 paired box 3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8661050 1552573 Pax3 paired box 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11857794 1552573 Pax3 paired box 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17418413 1552573 Pax3 paired box 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21867959 1552573 Pax3 paired box 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21512107 1552573 Pax3 paired box 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1552573 Pax3 paired box 3 gene MP:0011102 embryonic lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1552573 Pax3 paired box 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20095975 1552573 Pax3 paired box 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9344762 1552573 Pax3 paired box 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36400788 1552573 Pax3 paired box 3 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36400788 1552573 Pax3 paired box 3 gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21867959 1552573 Pax3 paired box 3 gene MP:0012169 optic placode degeneration IAGP N RGD:5509061 20141003 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0012185 abnormal muscle precursor cell morphology IAGP N RGD:5509061 20210513 MGI PMID:32094117 1552573 Pax3 paired box 3 gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20141003 MGI PMID:12242297 1552573 Pax3 paired box 3 gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20141003 MGI PMID:15132998 1552573 Pax3 paired box 3 gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20141003 MGI PMID:18483623 1552573 Pax3 paired box 3 gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20231109 MGI PMID:36400788 1552573 Pax3 paired box 3 gene MP:0012547 spina bifida cystica IEA N RGD:5509061 20141003 MGI 1552573 Pax3 paired box 3 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11914272 1552573 Pax3 paired box 3 gene MP:0012728 abnormal somite border morphology IAGP N RGD:5509061 20141003 MGI PMID:14665670 1552573 Pax3 paired box 3 gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:2619088 1552573 Pax3 paired box 3 gene MP:0012745 abnormal neural crest cell physiology IAGP N RGD:5509061 20231102 MGI PMID:35899771 1552573 Pax3 paired box 3 gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20231102 MGI PMID:35899771 1552573 Pax3 paired box 3 gene MP:0013264 tongue ankylosis IAGP N RGD:5509061 20221020 MGI PMID:32692983 1552573 Pax3 paired box 3 gene MP:0013720 abnormal mammary line morphology IAGP N RGD:5509061 20150402 MGI PMID:16720875 1552573 Pax3 paired box 3 gene MP:0013721 abnormal mammary placode morphology IAGP N RGD:5509061 20150402 MGI PMID:16720875 1552573 Pax3 paired box 3 gene MP:0013848 subcutaneous edema IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20221020 MGI PMID:32692983 1552573 Pax3 paired box 3 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20170824 MGI PMID:28043919 1552573 Pax3 paired box 3 gene MP:0014167 ectopic bone IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20221013 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0021095 abnormal dorsal interneuron 4 morphology IAGP N RGD:5509061 20220310 MGI PMID:18198335 1552573 Pax3 paired box 3 gene MP:0021210 bilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:32692983 1552573 Pax3 paired box 3 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:31241461 1552573 Pax3 paired box 3 gene MP:0021216 abnormal palatal mesenchymal cell differentiation IAGP N RGD:5509061 20230302 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0021217 abnormal palatal shelf bone ossification IAGP N RGD:5509061 20230302 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0030056 lacrimal bone hypoplasia IAGP N RGD:5509061 20170921 MGI PMID:15520281 1552573 Pax3 paired box 3 gene MP:0030190 small snout IAGP N RGD:5509061 20230309 MGI PMID:23872235 1552573 Pax3 paired box 3 gene MP:0030291 short soft palate IAGP N RGD:5509061 20221020 MGI PMID:17927973 1552573 Pax3 paired box 3 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20230309 MGI PMID:23872235 1552573 Pax3 paired box 3 gene MP:0030535 abnormal hypoglossal cord morphology IAGP N RGD:5509061 20180125 MGI PMID:16951257 1552573 Pax3 paired box 3 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:32692983 1552573 Pax3 paired box 3 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:9344762 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230119 MGI 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12213450 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12213450 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23269668 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:23269668 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23269668 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:12213450 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12213450 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:12213450 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0003370 increased circulating estrogen level IAGP N RGD:5509061 20141003 MGI PMID:23269668 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:23269668 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:23269668 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230119 MGI 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230119 MGI 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23269668 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230119 MGI 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20230119 MGI 1552574 Chst10 carbohydrate sulfotransferase 10 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230119 MGI 1552575 Plpp7 phospholipid phosphatase 7 (inactive) gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20210311 MGI PMID:33514739 1552575 Plpp7 phospholipid phosphatase 7 (inactive) gene MP:0000747 muscle weakness IAGP N RGD:5509061 20210311 MGI PMID:33514739 1552575 Plpp7 phospholipid phosphatase 7 (inactive) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20210311 MGI PMID:33514739 1552575 Plpp7 phospholipid phosphatase 7 (inactive) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210311 MGI PMID:33514739 1552575 Plpp7 phospholipid phosphatase 7 (inactive) gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20210311 MGI PMID:33514739 1552575 Plpp7 phospholipid phosphatase 7 (inactive) gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20210311 MGI PMID:33514739 1552575 Plpp7 phospholipid phosphatase 7 (inactive) gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20210311 MGI PMID:33514739 1552575 Plpp7 phospholipid phosphatase 7 (inactive) gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20210311 MGI PMID:33514739 1552575 Plpp7 phospholipid phosphatase 7 (inactive) gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20210311 MGI PMID:33514739 1552575 Plpp7 phospholipid phosphatase 7 (inactive) gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20210311 MGI PMID:33514739 1552575 Plpp7 phospholipid phosphatase 7 (inactive) gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20210311 MGI PMID:33514739 1552575 Plpp7 phospholipid phosphatase 7 (inactive) gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20210311 MGI PMID:33514739 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:12486155 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10688600 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11961069 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12486155 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0000742 impaired contractility of ileal smooth muscle IAGP N RGD:5509061 20141003 MGI PMID:12486155 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9990086 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:18382674 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:10688600 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12486155 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:9990086 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15919709 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:12486155 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:18382674 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:16110248 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0005085 abnormal gallbladder physiology IAGP N RGD:5509061 20141003 MGI PMID:11961069 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9990086 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10688600 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9990086 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0012125 decreased bronchoconstrictive response IAGP N RGD:5509061 20141003 MGI PMID:14645675 1552578 Chrm2 cholinergic receptor, muscarinic 2, cardiac gene MP:0031650 decreased mounting behavior IAGP N RGD:5509061 20240905 MGI PMID:18382674 1552581 Fgfbp1 fibroblast growth factor binding protein 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20170706 MGI PMID:28053031 1552581 Fgfbp1 fibroblast growth factor binding protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20170706 MGI PMID:28053031 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9664684 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000084 abnormal fontanelle morphology IAGP N RGD:5509061 20141003 MGI PMID:9664684 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:9664684 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20141003 MGI PMID:20215352 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17166916 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000828 abnormal fourth ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19741143 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17166916 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:19741143 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17166916 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19741143 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:19741143 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:17166916 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:17166916 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:21752929 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15562281 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001296 macrophthalmia IAGP N RGD:5509061 20141218 MGI PMID:11929848 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10660670 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141218 MGI PMID:11929848 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001316 cornea scarring IAGP N RGD:5509061 20141218 MGI PMID:11929848 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001316 cornea scarring IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20141003 MGI PMID:10660670 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20141218 MGI PMID:11929848 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141218 MGI PMID:11929848 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18695238 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001375 abnormal mating preference IAGP N RGD:5509061 20141003 MGI PMID:21441904 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150827 MGI PMID:25915474 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9590288 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18695238 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:18695238 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:9590288 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141218 MGI PMID:11929848 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15007643 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19298015 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20150827 MGI PMID:25915474 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18695238 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20150827 MGI PMID:25915474 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:17316599 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20171102 MGI PMID:9664684 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:17316599 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15562281 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002892 decreased superior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:17166916 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:20215352 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:11956245 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20150827 MGI PMID:25915474 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20215352 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20150827 MGI PMID:25915474 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10660670 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21752929 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:17316599 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0003687 abnormal intraocular muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0003877 abnormal serotonergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17151281 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:18695238 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004096 abnormal midbrain-hindbrain boundary development IAGP N RGD:5509061 20141003 MGI PMID:17166916 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004224 absent trabecular meshwork IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004284 abnormal Descemet membrane morphology IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004343 small scapula IAGP N RGD:5509061 20141003 MGI PMID:9590288 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004360 absent ulna IAGP N RGD:5509061 20141003 MGI PMID:9590288 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004443 absent supraoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:9664684 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004508 abnormal pectoral girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9590288 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004688 absent ilium IAGP N RGD:5509061 20141003 MGI PMID:9590288 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004694 absent patella IAGP N RGD:5509061 20141003 MGI PMID:20215352 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004694 absent patella IAGP N RGD:5509061 20141003 MGI PMID:9590288 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20150827 MGI PMID:25915474 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004861 abnormal Raphe nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:17151281 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004861 abnormal Raphe nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18695238 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:21752929 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20150827 MGI PMID:25915474 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20141003 MGI PMID:10660670 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:10660670 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005208 abnormal iris stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:10660670 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17316599 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9590288 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:10660670 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20160310 MGI PMID:11929848 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20160310 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11956245 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17316599 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11956244 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11956245 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:20215352 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:20215352 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20150827 MGI PMID:25915474 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20141003 MGI PMID:17166916 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0006105 small tectum IAGP N RGD:5509061 20141003 MGI PMID:17166916 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0006230 iris stroma hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:19298015 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:11956244 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:17316599 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20141003 MGI PMID:11956244 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20141003 MGI PMID:11956245 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20141003 MGI PMID:17316599 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0008138 absent podocyte foot process IAGP N RGD:5509061 20141003 MGI PMID:11956245 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:17316599 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20150827 MGI PMID:25915474 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:18695238 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0008494 absence of all nails IAGP N RGD:5509061 20141003 MGI PMID:9590288 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20150827 MGI PMID:25915474 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20150827 MGI PMID:25915474 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:21752929 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21752929 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0009274 buphthalmos IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20150827 MGI PMID:25915474 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0009637 abnormal pretectal region morphology IAGP N RGD:5509061 20141003 MGI PMID:17166916 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0009825 cornea ulcer IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:21246047 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17316599 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9590288 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:11956245 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11956245 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:9590288 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:17316599 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:17316599 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:9590288 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:21752929 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11956245 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011455 absent glomerular endothelium fenestra IAGP N RGD:5509061 20141003 MGI PMID:11956245 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141218 MGI PMID:11929848 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0011483 renal glomerular synechia IAGP N RGD:5509061 20141003 MGI PMID:17316599 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0012000 abnormal limb position IAGP N RGD:5509061 20141218 MGI PMID:24809698 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20141003 MGI PMID:17166916 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0012785 decreased rhombomere 1 size IAGP N RGD:5509061 20141003 MGI PMID:17166916 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0013742 absent ciliary body IAGP N RGD:5509061 20150416 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0013743 ciliary body hypoplasia IAGP N RGD:5509061 20150416 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:25915474 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:21441904 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0031212 decreased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:10660670 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0031212 decreased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:20568247 1552590 Lmx1b LIM homeobox transcription factor 1 beta gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:25915474 1552591 Hsp90ab1 heat shock protein 90 alpha (cytosolic), class B member 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10654595 1552591 Hsp90ab1 heat shock protein 90 alpha (cytosolic), class B member 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:10654595 1552591 Hsp90ab1 heat shock protein 90 alpha (cytosolic), class B member 1 gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:10654595 1552591 Hsp90ab1 heat shock protein 90 alpha (cytosolic), class B member 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10654595 1552591 Hsp90ab1 heat shock protein 90 alpha (cytosolic), class B member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10654595 1552591 Hsp90ab1 heat shock protein 90 alpha (cytosolic), class B member 1 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:10654595 1552592 Usp37 ubiquitin specific peptidase 37 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1552592 Usp37 ubiquitin specific peptidase 37 gene MP:0011092 embryonic lethality, complete penetrance IEA N RGD:5509061 20200310 MGI 1552592 Usp37 ubiquitin specific peptidase 37 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552593 Marveld3 MARVEL (membrane-associating) domain containing 3 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20230601 MGI 1552593 Marveld3 MARVEL (membrane-associating) domain containing 3 gene MP:0000154 rib fusion IEA N RGD:5509061 20230601 MGI 1552593 Marveld3 MARVEL (membrane-associating) domain containing 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1552593 Marveld3 MARVEL (membrane-associating) domain containing 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1552593 Marveld3 MARVEL (membrane-associating) domain containing 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1552593 Marveld3 MARVEL (membrane-associating) domain containing 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1552593 Marveld3 MARVEL (membrane-associating) domain containing 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1552593 Marveld3 MARVEL (membrane-associating) domain containing 3 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230601 MGI 1552593 Marveld3 MARVEL (membrane-associating) domain containing 3 gene MP:0003036 vertebral transformation IEA N RGD:5509061 20230601 MGI 1552593 Marveld3 MARVEL (membrane-associating) domain containing 3 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20230601 MGI 1552593 Marveld3 MARVEL (membrane-associating) domain containing 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1552593 Marveld3 MARVEL (membrane-associating) domain containing 3 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20230601 MGI 1552593 Marveld3 MARVEL (membrane-associating) domain containing 3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230601 MGI 1552596 Depdc1a DEP domain containing 1a gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 1552596 Depdc1a DEP domain containing 1a gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1552600 Plekhm2 pleckstrin homology domain containing, family M (with RUN domain) member 2 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20200310 MGI 1552600 Plekhm2 pleckstrin homology domain containing, family M (with RUN domain) member 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:26268777 1552600 Plekhm2 pleckstrin homology domain containing, family M (with RUN domain) member 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20200310 MGI 1552600 Plekhm2 pleckstrin homology domain containing, family M (with RUN domain) member 2 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:26268777 1552600 Plekhm2 pleckstrin homology domain containing, family M (with RUN domain) member 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20200310 MGI 1552600 Plekhm2 pleckstrin homology domain containing, family M (with RUN domain) member 2 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20200310 MGI PMID:26268777 1552600 Plekhm2 pleckstrin homology domain containing, family M (with RUN domain) member 2 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:26268777 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20201224 MGI PMID:29617460 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20201224 MGI PMID:29617460 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20201224 MGI PMID:29617460 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20201224 MGI PMID:29617460 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20201224 MGI PMID:29617460 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22952456 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:11431694 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:11431694 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:22952456 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:22952456 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20201224 MGI PMID:29617460 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22952456 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:22952456 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:22952456 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20201224 MGI PMID:29617460 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:22952456 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20201224 MGI PMID:29617460 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20201224 MGI PMID:29617460 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20201224 MGI PMID:29617460 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20201224 MGI PMID:29617460 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11431694 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0013916 decreased intestine length IAGP N RGD:5509061 20201224 MGI PMID:29617460 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0014078 small intestinal villus atrophy IAGP N RGD:5509061 20201224 MGI PMID:29617460 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0014222 decreased colon goblet cell number IAGP N RGD:5509061 20201224 MGI PMID:29617460 1552601 Spint2 serine protease inhibitor, Kunitz type 2 gene MP:0031154 intestinal hemorrhage IAGP N RGD:5509061 20201224 MGI PMID:29617460 1552604 Amigo1 adhesion molecule with Ig like domain 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1552604 Amigo1 adhesion molecule with Ig like domain 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210826 MGI 1552604 Amigo1 adhesion molecule with Ig like domain 1 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20230413 MGI PMID:35169021 1552604 Amigo1 adhesion molecule with Ig like domain 1 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20230413 MGI PMID:35169021 1552608 Kif3a kinesin family member 3A gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:17359961 1552608 Kif3a kinesin family member 3A gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:17359961 1552608 Kif3a kinesin family member 3A gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17359961 1552608 Kif3a kinesin family member 3A gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17359961 1552608 Kif3a kinesin family member 3A gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:10220415 1552608 Kif3a kinesin family member 3A gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:12672950 1552608 Kif3a kinesin family member 3A gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17166921 1552608 Kif3a kinesin family member 3A gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:17166921 1552608 Kif3a kinesin family member 3A gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15755804 1552608 Kif3a kinesin family member 3A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17166921 1552608 Kif3a kinesin family member 3A gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:23332756 1552608 Kif3a kinesin family member 3A gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10220415 1552608 Kif3a kinesin family member 3A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23332756 1552608 Kif3a kinesin family member 3A gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10220415 1552608 Kif3a kinesin family member 3A gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10220415 1552608 Kif3a kinesin family member 3A gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15755804 1552608 Kif3a kinesin family member 3A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12672950 1552608 Kif3a kinesin family member 3A gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:10220415 1552608 Kif3a kinesin family member 3A gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0001925 male infertility IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21209331 1552608 Kif3a kinesin family member 3A gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:21745638 1552608 Kif3a kinesin family member 3A gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:17359961 1552608 Kif3a kinesin family member 3A gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:18579360 1552608 Kif3a kinesin family member 3A gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:10220415 1552608 Kif3a kinesin family member 3A gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17359961 1552608 Kif3a kinesin family member 3A gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:12672950 1552608 Kif3a kinesin family member 3A gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12672950 1552608 Kif3a kinesin family member 3A gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:12672950 1552608 Kif3a kinesin family member 3A gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:17359961 1552608 Kif3a kinesin family member 3A gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12672950 1552608 Kif3a kinesin family member 3A gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:10220415 1552608 Kif3a kinesin family member 3A gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20200130 MGI PMID:10943838 1552608 Kif3a kinesin family member 3A gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:23332756 1552608 Kif3a kinesin family member 3A gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:10220415 1552608 Kif3a kinesin family member 3A gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:10220415 1552608 Kif3a kinesin family member 3A gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:10220415 1552608 Kif3a kinesin family member 3A gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:21209331 1552608 Kif3a kinesin family member 3A gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:10220415 1552608 Kif3a kinesin family member 3A gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:17359961 1552608 Kif3a kinesin family member 3A gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:17166921 1552608 Kif3a kinesin family member 3A gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:17359961 1552608 Kif3a kinesin family member 3A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0004911 absent mandibular condyloid process IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:12672950 1552608 Kif3a kinesin family member 3A gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:17359961 1552608 Kif3a kinesin family member 3A gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:12672950 1552608 Kif3a kinesin family member 3A gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:17166921 1552608 Kif3a kinesin family member 3A gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:10220415 1552608 Kif3a kinesin family member 3A gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20171109 MGI PMID:10220415 1552608 Kif3a kinesin family member 3A gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:17166921 1552608 Kif3a kinesin family member 3A gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:17166921 1552608 Kif3a kinesin family member 3A gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:18579360 1552608 Kif3a kinesin family member 3A gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18579360 1552608 Kif3a kinesin family member 3A gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200130 MGI PMID:10943838 1552608 Kif3a kinesin family member 3A gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:12672950 1552608 Kif3a kinesin family member 3A gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:18579360 1552608 Kif3a kinesin family member 3A gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20200130 MGI PMID:10943838 1552608 Kif3a kinesin family member 3A gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200130 MGI PMID:10943838 1552608 Kif3a kinesin family member 3A gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0009328 delayed heart looping IAGP N RGD:5509061 20141003 MGI PMID:10220415 1552608 Kif3a kinesin family member 3A gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:18579360 1552608 Kif3a kinesin family member 3A gene MP:0010500 myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10220415 1552608 Kif3a kinesin family member 3A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 1552608 Kif3a kinesin family member 3A gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20141003 MGI PMID:12672950 1552608 Kif3a kinesin family member 3A gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:12672950 1552608 Kif3a kinesin family member 3A gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12672950 1552608 Kif3a kinesin family member 3A gene MP:0012093 absent nodal flow IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0012509 neural tube degeneration IAGP N RGD:5509061 20141003 MGI PMID:10330409 1552608 Kif3a kinesin family member 3A gene MP:0012754 abnormal cranial neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0012759 increased cranial neural crest cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0014468 disorganized sperm mitochondrial sheath IAGP N RGD:5509061 20240613 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0020384 absent kidney epithelial cell primary cilium IAGP N RGD:5509061 20161013 MGI PMID:12672950 1552608 Kif3a kinesin family member 3A gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20190704 MGI PMID:17359961 1552608 Kif3a kinesin family member 3A gene MP:0030251 broad frontonasal prominence IAGP N RGD:5509061 20171019 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0030269 absent mandibular ramus IAGP N RGD:5509061 20171026 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0030276 anterior cranium occultum IAGP N RGD:5509061 20171102 MGI PMID:20106874 1552608 Kif3a kinesin family member 3A gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220324 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0031373 abnormal manchette perinuclear ring morphology IAGP N RGD:5509061 20220407 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0031375 abnormal manchette disassembly IAGP N RGD:5509061 20220407 MGI PMID:23831641 1552608 Kif3a kinesin family member 3A gene MP:0031386 elongated manchette IAGP N RGD:5509061 20220428 MGI PMID:23831641 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210128 MGI 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210128 MGI 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0009453 enhanced contextual conditioning behavior IEA N RGD:5509061 20210128 MGI 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0009787 increased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20190110 MGI PMID:30442668 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20190110 MGI PMID:30442668 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1552609 Marchf3 membrane associated ring-CH-type finger 3 gene MP:0020148 abnormal susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20190110 MGI PMID:30442668 1552610 Eif4a1 eukaryotic translation initiation factor 4A1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20240627 MGI PMID:38011999 1552610 Eif4a1 eukaryotic translation initiation factor 4A1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20240627 MGI PMID:38011999 1552610 Eif4a1 eukaryotic translation initiation factor 4A1 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20240627 MGI PMID:38011999 1552610 Eif4a1 eukaryotic translation initiation factor 4A1 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20240627 MGI PMID:38011999 1552610 Eif4a1 eukaryotic translation initiation factor 4A1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20240627 MGI PMID:38011999 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:10922077 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:10922077 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10922077 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10922077 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0001399 hyperactivity IEA N RGD:5509061 20170105 MGI 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20170105 MGI 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:10922077 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:16600521 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:11584074 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10922077 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:10922077 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:10922077 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0003063 increased coping response IEA N RGD:5509061 20240523 MGI 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210520 MGI 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:16600521 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:10922077 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:10922077 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:16600521 1552611 Ppp1r9b protein phosphatase 1, regulatory subunit 9B gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20160421 MGI 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19287392 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20201022 MGI 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0001147 small testis IEA N RGD:5509061 20201022 MGI 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20201022 MGI 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20201022 MGI 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19287392 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0002323 decreased susceptibility to hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:19287392 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19287392 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19732742 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19287392 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19287392 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19287392 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19287392 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19287392 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:19287392 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:19287392 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:19287392 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19287392 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0009128 decreased brown fat cell number IAGP N RGD:5509061 20141003 MGI PMID:19287392 1552612 Mogat2 monoacylglycerol O-acyltransferase 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1552615 Rpl32 ribosomal protein L32 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1552619 Grin3a glutamate receptor ionotropic, NMDA3A gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1552619 Grin3a glutamate receptor ionotropic, NMDA3A gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20200514 MGI 1552619 Grin3a glutamate receptor ionotropic, NMDA3A gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:15866554 1552619 Grin3a glutamate receptor ionotropic, NMDA3A gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:9620802 1552619 Grin3a glutamate receptor ionotropic, NMDA3A gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:14507892 1552619 Grin3a glutamate receptor ionotropic, NMDA3A gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:9620802 1552620 Dnaaf1 dynein, axonemal assembly factor 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1552620 Dnaaf1 dynein, axonemal assembly factor 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20200310 MGI PMID:23968836 1552620 Dnaaf1 dynein, axonemal assembly factor 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200310 MGI PMID:23968836 1552620 Dnaaf1 dynein, axonemal assembly factor 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20200310 MGI PMID:23968836 1552620 Dnaaf1 dynein, axonemal assembly factor 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20200310 MGI PMID:23968836 1552620 Dnaaf1 dynein, axonemal assembly factor 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20200310 MGI PMID:23968836 1552620 Dnaaf1 dynein, axonemal assembly factor 1 gene MP:0010511 shortened PR interval IEA N RGD:5509061 20231207 MGI 1552620 Dnaaf1 dynein, axonemal assembly factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23968836 1552620 Dnaaf1 dynein, axonemal assembly factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1552621 Cnot1 CCR4-NOT transcription complex, subunit 1 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20200310 MGI PMID:29438013 1552621 Cnot1 CCR4-NOT transcription complex, subunit 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:29438013 1552621 Cnot1 CCR4-NOT transcription complex, subunit 1 gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20200310 MGI PMID:29438013 1552621 Cnot1 CCR4-NOT transcription complex, subunit 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29438013 1552625 Nmur1 neuromedin U receptor 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:17379411 1552625 Nmur1 neuromedin U receptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:19070594 1552625 Nmur1 neuromedin U receptor 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20200310 MGI PMID:16474416 1552625 Nmur1 neuromedin U receptor 1 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 1552629 Nr1i3 nuclear receptor subfamily 1, group I, member 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18941143 1552629 Nr1i3 nuclear receptor subfamily 1, group I, member 3 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:12644704 1552629 Nr1i3 nuclear receptor subfamily 1, group I, member 3 gene MP:0005469 abnormal thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:15004031 1552629 Nr1i3 nuclear receptor subfamily 1, group I, member 3 gene MP:0005472 abnormal triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:15004031 1552629 Nr1i3 nuclear receptor subfamily 1, group I, member 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15340055 1552629 Nr1i3 nuclear receptor subfamily 1, group I, member 3 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12376703 1552629 Nr1i3 nuclear receptor subfamily 1, group I, member 3 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18677425 1552629 Nr1i3 nuclear receptor subfamily 1, group I, member 3 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11057673 1552629 Nr1i3 nuclear receptor subfamily 1, group I, member 3 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12376703 1552629 Nr1i3 nuclear receptor subfamily 1, group I, member 3 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12644704 1552629 Nr1i3 nuclear receptor subfamily 1, group I, member 3 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15004031 1552629 Nr1i3 nuclear receptor subfamily 1, group I, member 3 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18677425 1552629 Nr1i3 nuclear receptor subfamily 1, group I, member 3 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:18677425 1552629 Nr1i3 nuclear receptor subfamily 1, group I, member 3 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:15004031 1552629 Nr1i3 nuclear receptor subfamily 1, group I, member 3 gene MP:0010951 abnormal lipid oxidation IAGP N RGD:5509061 20141003 MGI PMID:18941143 1552631 Skp2 S-phase kinase-associated protein 2 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10790373 1552631 Skp2 S-phase kinase-associated protein 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10790373 1552631 Skp2 S-phase kinase-associated protein 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11861371 1552631 Skp2 S-phase kinase-associated protein 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:10790373 1552631 Skp2 S-phase kinase-associated protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10790373 1552631 Skp2 S-phase kinase-associated protein 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:10790373 1552631 Skp2 S-phase kinase-associated protein 2 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:11818378 1552631 Skp2 S-phase kinase-associated protein 2 gene MP:0008755 abnormal immunoglobulin V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:21349429 1552631 Skp2 S-phase kinase-associated protein 2 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:10790373 1552632 Cd320 CD320 antigen gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:23430977 1552632 Cd320 CD320 antigen gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:23430977 1552632 Cd320 CD320 antigen gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20200310 MGI 1552632 Cd320 CD320 antigen gene MP:0004019 abnormal vitamin homeostasis IAGP N RGD:5509061 20200310 MGI PMID:23430977 1552632 Cd320 CD320 antigen gene MP:0011227 abnormal vitamin B12 level IAGP N RGD:5509061 20200310 MGI PMID:23430977 1552632 Cd320 CD320 antigen gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20220811 MGI 1552632 Cd320 CD320 antigen gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20200310 MGI PMID:23430977 1552632 Cd320 CD320 antigen gene MP:0030628 increased methylmalonic acid level IAGP N RGD:5509061 20200310 MGI PMID:23430977 1552632 Cd320 CD320 antigen gene MP:0030630 increased circulating methylmalonic acid level IAGP N RGD:5509061 20200310 MGI PMID:23430977 1552634 Tspan11 tetraspanin 11 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20210128 MGI 1552634 Tspan11 tetraspanin 11 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20210128 MGI 1552636 Kcnk18 potassium channel, subfamily K, member 18 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170105 MGI 1552636 Kcnk18 potassium channel, subfamily K, member 18 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20141003 MGI PMID:17962323 1552636 Kcnk18 potassium channel, subfamily K, member 18 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:17962323 1552636 Kcnk18 potassium channel, subfamily K, member 18 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20170105 MGI 1552636 Kcnk18 potassium channel, subfamily K, member 18 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:17962323 1552637 Zbtb4 zinc finger and BTB domain containing 4 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20200310 MGI 1552637 Zbtb4 zinc finger and BTB domain containing 4 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1552637 Zbtb4 zinc finger and BTB domain containing 4 gene MP:0001307 fused cornea and lens IEA N RGD:5509061 20200310 MGI 1552637 Zbtb4 zinc finger and BTB domain containing 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1552637 Zbtb4 zinc finger and BTB domain containing 4 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 1552637 Zbtb4 zinc finger and BTB domain containing 4 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1552637 Zbtb4 zinc finger and BTB domain containing 4 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20201231 MGI 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20421483 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:15340140 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0000962 disorganized dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:16155866 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11875122 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16155866 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16155866 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11875122 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16155866 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:12004056 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15340140 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16155866 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:20421483 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:19074277 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11875122 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15340140 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16155866 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20421483 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0002963 decreased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11875122 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:16155866 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20421483 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20421483 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16155866 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16155866 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16155866 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:20421483 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0010079 increased osteochondroma incidence IAGP N RGD:5509061 20141003 MGI PMID:20421483 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0010280 increased skeletal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20421483 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0010280 increased skeletal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20940146 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:16155866 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0010971 abnormal periosteum morphology IAGP N RGD:5509061 20141003 MGI PMID:20421483 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11875122 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552640 Prkaca protein kinase, cAMP dependent, catalytic, alpha gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11886853 1552646 Or5an6 olfactory receptor family 5 subfamily AN member 6 gene MP:0020852 abnormal olfactory behavior IAGP N RGD:5509061 20200917 MGI PMID:30643144 1552647 Wdr12 WD repeat domain 12 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20170105 MGI 1552647 Wdr12 WD repeat domain 12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552647 Wdr12 WD repeat domain 12 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1552647 Wdr12 WD repeat domain 12 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1552648 Ankib1 ankyrin repeat and IBR domain containing 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20200310 MGI 1552648 Ankib1 ankyrin repeat and IBR domain containing 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1552648 Ankib1 ankyrin repeat and IBR domain containing 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1552648 Ankib1 ankyrin repeat and IBR domain containing 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1552648 Ankib1 ankyrin repeat and IBR domain containing 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20200310 MGI 1552649 Fstl4 follistatin-like 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:18253481 1552650 Acvr1c activin A receptor, type IC gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210826 MGI 1552650 Acvr1c activin A receptor, type IC gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15485907 1552650 Acvr1c activin A receptor, type IC gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16564040 1552650 Acvr1c activin A receptor, type IC gene MP:0002833 increased heart weight IEA N RGD:5509061 20201022 MGI 1552650 Acvr1c activin A receptor, type IC gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20231109 MGI PMID:37093546 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0001163 abnormal prostate gland anterior lobe morphology IAGP N RGD:5509061 20231109 MGI PMID:37093546 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230223 MGI PMID:30126926 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0002083 premature death IAGP N RGD:5509061 20230223 MGI PMID:30126926 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0002083 premature death IAGP N RGD:5509061 20231109 MGI PMID:37093546 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20230223 MGI PMID:30126926 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20230223 MGI PMID:30126926 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0003608 prostate gland inflammation IAGP N RGD:5509061 20231109 MGI PMID:37093546 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20230223 MGI PMID:30126926 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0005305 prostate gland anterior lobe hyperplasia IAGP N RGD:5509061 20231109 MGI PMID:37093546 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20230223 MGI PMID:30126926 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20230223 MGI PMID:30126926 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20231109 MGI PMID:37093546 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0009381 abnormal prostate gland dorsolateral lobe morphology IAGP N RGD:5509061 20231109 MGI PMID:37093546 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20230223 MGI PMID:30126926 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20230223 MGI PMID:30126926 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20230223 MGI PMID:30126926 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20230223 MGI PMID:30126926 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20230223 MGI PMID:30126926 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0013320 dilated seminal vesicle IAGP N RGD:5509061 20231109 MGI PMID:37093546 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0013899 abnormal seminal vesicle epithelium morphology IAGP N RGD:5509061 20231109 MGI PMID:37093546 1552652 Elac2 elaC ribonuclease Z 2 gene MP:0031369 prostate gland dorsolateral lobe hyperplasia IAGP N RGD:5509061 20231109 MGI PMID:37093546 1552653 Mast4 microtubule associated serine/threonine kinase family member 4 gene MP:0000120 malocclusion IEA N RGD:5509061 20200310 MGI 1552653 Mast4 microtubule associated serine/threonine kinase family member 4 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20240926 MGI PMID:33219327 1552653 Mast4 microtubule associated serine/threonine kinase family member 4 gene MP:0001147 small testis IAGP N RGD:5509061 20240926 MGI PMID:33219327 1552653 Mast4 microtubule associated serine/threonine kinase family member 4 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20240926 MGI PMID:33219327 1552653 Mast4 microtubule associated serine/threonine kinase family member 4 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20240926 MGI PMID:33219327 1552653 Mast4 microtubule associated serine/threonine kinase family member 4 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20240926 MGI PMID:33219327 1552653 Mast4 microtubule associated serine/threonine kinase family member 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240926 MGI PMID:33219327 1552653 Mast4 microtubule associated serine/threonine kinase family member 4 gene MP:0011416 abnormal testis interstitial tissue morphology IAGP N RGD:5509061 20240926 MGI PMID:33219327 1552653 Mast4 microtubule associated serine/threonine kinase family member 4 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20240926 MGI PMID:33219327 1552654 Pdgfd platelet-derived growth factor, D polypeptide gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20191017 MGI PMID:27032083 1552654 Pdgfd platelet-derived growth factor, D polypeptide gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 1552654 Pdgfd platelet-derived growth factor, D polypeptide gene MP:0001260 increased body weight IAGP N RGD:5509061 20191017 MGI PMID:27032083 1552654 Pdgfd platelet-derived growth factor, D polypeptide gene MP:0001935 decreased litter size IAGP N RGD:5509061 20191017 MGI PMID:27032083 1552654 Pdgfd platelet-derived growth factor, D polypeptide gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1552654 Pdgfd platelet-derived growth factor, D polypeptide gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20191017 MGI PMID:27032083 1552654 Pdgfd platelet-derived growth factor, D polypeptide gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20191017 MGI PMID:27032083 1552654 Pdgfd platelet-derived growth factor, D polypeptide gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20210128 MGI 1552654 Pdgfd platelet-derived growth factor, D polypeptide gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20191017 MGI PMID:27032083 1552654 Pdgfd platelet-derived growth factor, D polypeptide gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20191017 MGI PMID:27032083 1552656 Clec14a C-type lectin domain family 14, member a gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20200310 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20141003 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20141003 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0000458 abnormal mandible morphology IEA N RGD:5509061 20141003 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0001258 decreased body length IEA N RGD:5509061 20160804 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20141003 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20160421 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20141003 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20141003 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0005358 abnormal incisor morphology IEA N RGD:5509061 20141003 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20160421 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20160804 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20141003 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20141003 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20141003 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0010093 decreased circulating magnesium level IEA N RGD:5509061 20201022 MGI 1552659 Slc25a21 solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20141003 MGI 1552660 Chmp4b charged multivesicular body protein 4B gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17683935 1552661 Cpa5 carboxypeptidase A5 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220519 MGI 1552661 Cpa5 carboxypeptidase A5 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1552661 Cpa5 carboxypeptidase A5 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220519 MGI 1552665 Snx11 sorting nexin 11 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20210923 MGI PMID:31730264 1552665 Snx11 sorting nexin 11 gene MP:0003663 abnormal thermosensation IAGP N RGD:5509061 20210923 MGI PMID:31730264 1552665 Snx11 sorting nexin 11 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20210923 MGI PMID:31730264 1552667 Desi2 desumoylating isopeptidase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21553223 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0000537 abnormal urethra morphology IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0000753 paralysis IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0000909 abnormal facial motor nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0000958 peripheral nervous system degeneration IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0001177 atelectasis IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0001334 absent optic tract IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20220519 MGI 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0001948 vesicoureteral reflux IAGP N RGD:5509061 20240926 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210826 MGI 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20220519 MGI 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0003624 anuria IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0008492 dorsal root ganglion degeneration IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0010057 abnormal olfactory bulb outer nerve layer morphology IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20200310 MGI PMID:23082226 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552668 Nmnat2 nicotinamide nucleotide adenylyltransferase 2 gene MP:0012484 decreased corticospinal tract size IAGP N RGD:5509061 20200310 MGI PMID:23946398 1552671 Phtf1 putative homeodomain transcription factor 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1552671 Phtf1 putative homeodomain transcription factor 1 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20181227 MGI 1552671 Phtf1 putative homeodomain transcription factor 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1552673 Gpc4 glypican 4 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20240523 MGI 1552673 Gpc4 glypican 4 gene MP:0001314 cornea opacity IEA N RGD:5509061 20230601 MGI 1552673 Gpc4 glypican 4 gene MP:0001577 anemia IEA N RGD:5509061 20141003 MGI 1552673 Gpc4 glypican 4 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20240523 MGI 1552673 Gpc4 glypican 4 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1552673 Gpc4 glypican 4 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20240523 MGI 1552673 Gpc4 glypican 4 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1552673 Gpc4 glypican 4 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20240523 MGI 1552673 Gpc4 glypican 4 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1552673 Gpc4 glypican 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1552673 Gpc4 glypican 4 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1552674 Sftpa1 surfactant associated protein A1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:12376353 1552674 Sftpa1 surfactant associated protein A1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:12376353 1552674 Sftpa1 surfactant associated protein A1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20200310 MGI PMID:12376353 1552674 Sftpa1 surfactant associated protein A1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:12740217 1552674 Sftpa1 surfactant associated protein A1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:12060563 1552674 Sftpa1 surfactant associated protein A1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:9126996 1552674 Sftpa1 surfactant associated protein A1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20200310 MGI PMID:11867335 1552674 Sftpa1 surfactant associated protein A1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20200310 MGI PMID:12376353 1552674 Sftpa1 surfactant associated protein A1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:11237812 1552674 Sftpa1 surfactant associated protein A1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:17967856 1552674 Sftpa1 surfactant associated protein A1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:9126996 1552674 Sftpa1 surfactant associated protein A1 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20200310 MGI PMID:12060563 1552674 Sftpa1 surfactant associated protein A1 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20200310 MGI PMID:12376353 1552674 Sftpa1 surfactant associated protein A1 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20200310 MGI PMID:16917077 1552674 Sftpa1 surfactant associated protein A1 gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20200310 MGI PMID:11867335 1552674 Sftpa1 surfactant associated protein A1 gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20200310 MGI PMID:12060563 1552674 Sftpa1 surfactant associated protein A1 gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20200310 MGI PMID:16917077 1552674 Sftpa1 surfactant associated protein A1 gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20200310 MGI PMID:9700084 1552674 Sftpa1 surfactant associated protein A1 gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20200310 MGI PMID:12376353 1552674 Sftpa1 surfactant associated protein A1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20200310 MGI PMID:11867335 1552674 Sftpa1 surfactant associated protein A1 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20200310 MGI PMID:11867335 1552674 Sftpa1 surfactant associated protein A1 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20200310 MGI PMID:11867335 1552674 Sftpa1 surfactant associated protein A1 gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20200310 MGI PMID:12740217 1552674 Sftpa1 surfactant associated protein A1 gene MP:0010898 abnormal pulmonary alveolus epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:12376353 1552674 Sftpa1 surfactant associated protein A1 gene MP:0010901 abnormal pulmonary alveolar parenchyma morphology IAGP N RGD:5509061 20200310 MGI PMID:11867335 1552674 Sftpa1 surfactant associated protein A1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17967856 1552674 Sftpa1 surfactant associated protein A1 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:11867335 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20200310 MGI PMID:19564410 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20200310 MGI PMID:11390367 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:20679483 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20200310 MGI PMID:17875667 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20200310 MGI PMID:17875667 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:19564410 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:19564410 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:17875667 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:19564410 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20200310 MGI PMID:17875667 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200310 MGI PMID:20679483 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20200310 MGI PMID:20679483 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20200310 MGI PMID:20679483 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20200310 MGI PMID:19564410 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:20679483 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20200310 MGI PMID:14515362 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20200310 MGI PMID:11562351 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:20679483 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20200310 MGI PMID:20679483 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19564410 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11390367 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20200310 MGI PMID:20679483 1552682 Mapk8ip1 mitogen-activated protein kinase 8 interacting protein 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:20679483 1552685 Vps16 VSP16 CORVET/HOPS core subunit gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20180301 MGI PMID:27174565 1552685 Vps16 VSP16 CORVET/HOPS core subunit gene MP:0005323 dystonia IAGP N RGD:5509061 20180301 MGI PMID:27174565 1552686 Or4e5 olfactory receptor family 4 subfamily E member 5 gene MP:0001003 abnormal olfactory receptor morphology IAGP N RGD:5509061 20141003 MGI PMID:24120133 1552686 Or4e5 olfactory receptor family 4 subfamily E member 5 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15157418 1552687 Sfxn3 sideroflexin 3 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0003325 decreased liver function IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552689 Degs1 delta 4-desaturase, sphingolipid 1 gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20200310 MGI PMID:17339025 1552696 Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:23479625 1552696 Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:23479625 1552696 Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23479625 1552696 Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:23479625 1552696 Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23479625 1552696 Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23479625 1552696 Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:23479625 1552696 Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23479625 1552696 Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23479625 1552696 Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:23479625 1552696 Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:23479625 1552696 Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 gene MP:0010332 abnormal circulating apolipoprotein level IAGP N RGD:5509061 20141003 MGI PMID:23479625 1552696 Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 gene MP:0010333 abnormal circulating apolipoprotein E level IAGP N RGD:5509061 20141003 MGI PMID:23479625 1552696 Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 gene MP:0011738 anasarca IAGP N RGD:5509061 20141003 MGI PMID:23479625 1552696 Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:23479625 1552701 Nufip1 nuclear FMR1 interacting protein 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20230119 MGI PMID:35982178 1552701 Nufip1 nuclear FMR1 interacting protein 1 gene MP:0009455 enhanced cued conditioning behavior IEA N RGD:5509061 20210128 MGI 1552701 Nufip1 nuclear FMR1 interacting protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552701 Nufip1 nuclear FMR1 interacting protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220811 MGI 1552701 Nufip1 nuclear FMR1 interacting protein 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1552701 Nufip1 nuclear FMR1 interacting protein 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1552703 Kif5b kinesin family member 5B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20870970 1552703 Kif5b kinesin family member 5B gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:20870970 1552703 Kif5b kinesin family member 5B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9657148 1552703 Kif5b kinesin family member 5B gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9657148 1552703 Kif5b kinesin family member 5B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20870970 1552703 Kif5b kinesin family member 5B gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:20870970 1552703 Kif5b kinesin family member 5B gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20870970 1552703 Kif5b kinesin family member 5B gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20870970 1552703 Kif5b kinesin family member 5B gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20870970 1552703 Kif5b kinesin family member 5B gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:20870970 1552703 Kif5b kinesin family member 5B gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:9657148 1552703 Kif5b kinesin family member 5B gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20870970 1552703 Kif5b kinesin family member 5B gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20870970 1552703 Kif5b kinesin family member 5B gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:9657148 1552703 Kif5b kinesin family member 5B gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20141003 MGI PMID:21335237 1552703 Kif5b kinesin family member 5B gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:20870970 1552703 Kif5b kinesin family member 5B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9657148 1552703 Kif5b kinesin family member 5B gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21335237 1552712 Hhat hedgehog acyltransferase gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20200310 MGI PMID:14975718 1552712 Hhat hedgehog acyltransferase gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20200310 MGI PMID:14975718 1552712 Hhat hedgehog acyltransferase gene MP:0000117 absent tooth placode IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0000120 malocclusion IAGP N RGD:5509061 20200310 MGI PMID:14975718 1552712 Hhat hedgehog acyltransferase gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0000445 short snout IAGP N RGD:5509061 20200310 MGI PMID:14975718 1552712 Hhat hedgehog acyltransferase gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0000565 oligodactyly IAGP N RGD:5509061 20200310 MGI PMID:15075292 1552712 Hhat hedgehog acyltransferase gene MP:0000565 oligodactyly IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0000926 absent floor plate IAGP N RGD:5509061 20200310 MGI PMID:15075292 1552712 Hhat hedgehog acyltransferase gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200310 MGI PMID:15075292 1552712 Hhat hedgehog acyltransferase gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20200310 MGI PMID:24784881 1552712 Hhat hedgehog acyltransferase gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:24784881 1552712 Hhat hedgehog acyltransferase gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20200310 MGI PMID:14975718 1552712 Hhat hedgehog acyltransferase gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:14975718 1552712 Hhat hedgehog acyltransferase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:15075292 1552712 Hhat hedgehog acyltransferase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20200310 MGI PMID:15075292 1552712 Hhat hedgehog acyltransferase gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20200310 MGI PMID:15075292 1552712 Hhat hedgehog acyltransferase gene MP:0003104 acrania IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20200310 MGI PMID:24784881 1552712 Hhat hedgehog acyltransferase gene MP:0004380 short frontal bone IAGP N RGD:5509061 20200310 MGI PMID:14975718 1552712 Hhat hedgehog acyltransferase gene MP:0004383 absent interparietal bone IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0004419 absent parietal bone IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0004443 absent supraoccipital bone IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0004445 small exoccipital bone IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0004447 small basioccipital bone IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0004471 short nasal bone IAGP N RGD:5509061 20200310 MGI PMID:14975718 1552712 Hhat hedgehog acyltransferase gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0004911 absent mandibular condyloid process IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0004913 absent mandibular angle IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20200310 MGI PMID:15075292 1552712 Hhat hedgehog acyltransferase gene MP:0006418 abnormal testis cord formation IAGP N RGD:5509061 20200310 MGI PMID:24784881 1552712 Hhat hedgehog acyltransferase gene MP:0008274 failure of bone ossification IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0009845 abnormal neural crest cell morphology IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0009846 abnormal neural crest morphology IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0010043 abnormal frontonasal suture morphology IAGP N RGD:5509061 20200310 MGI PMID:14975718 1552712 Hhat hedgehog acyltransferase gene MP:0010939 abnormal mandibular prominence morphology IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15075292 1552712 Hhat hedgehog acyltransferase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0012092 diencephalon hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0012247 absent cornea IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0013603 abnormal fetal Leydig cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:24784881 1552712 Hhat hedgehog acyltransferase gene MP:0013818 abnormal oral cavity morphology IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:15075292 1552712 Hhat hedgehog acyltransferase gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:15075292 1552712 Hhat hedgehog acyltransferase gene MP:0030200 abnormal nasal septum cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:14975718 1552712 Hhat hedgehog acyltransferase gene MP:0030249 small frontonasal prominence IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0030268 agnathia IAGP N RGD:5509061 20200310 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:23055936 1552712 Hhat hedgehog acyltransferase gene MP:0031450 nasal cartilage hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:23055936 1552714 Cmtm2a CKLF-like MARVEL transmembrane domain containing 2A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20190926 MGI PMID:30209135 1552714 Cmtm2a CKLF-like MARVEL transmembrane domain containing 2A gene MP:0001925 male infertility IAGP N RGD:5509061 20190926 MGI PMID:30209135 1552714 Cmtm2a CKLF-like MARVEL transmembrane domain containing 2A gene MP:0020869 immotile sperm IAGP N RGD:5509061 20190926 MGI PMID:30209135 1552714 Cmtm2a CKLF-like MARVEL transmembrane domain containing 2A gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20200102 MGI PMID:30209135 1552716 Dnm1 dynamin 1 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1552716 Dnm1 dynamin 1 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1552716 Dnm1 dynamin 1 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1552716 Dnm1 dynamin 1 gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:20700442 1552716 Dnm1 dynamin 1 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20200310 MGI PMID:20700442 1552716 Dnm1 dynamin 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1552716 Dnm1 dynamin 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1552716 Dnm1 dynamin 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:20700442 1552716 Dnm1 dynamin 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:20700442 1552716 Dnm1 dynamin 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20200310 MGI PMID:17463283 1552716 Dnm1 dynamin 1 gene MP:0001499 abnormal kindling response IAGP N RGD:5509061 20200310 MGI PMID:20700442 1552716 Dnm1 dynamin 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:20700442 1552716 Dnm1 dynamin 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:21689597 1552716 Dnm1 dynamin 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20200310 MGI PMID:20700442 1552716 Dnm1 dynamin 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:21689597 1552716 Dnm1 dynamin 1 gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20200310 MGI PMID:20700442 1552716 Dnm1 dynamin 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1552716 Dnm1 dynamin 1 gene MP:0002064 seizures IAGP N RGD:5509061 20200310 MGI PMID:27363778 1552716 Dnm1 dynamin 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200310 MGI PMID:17463283 1552716 Dnm1 dynamin 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200310 MGI PMID:20700442 1552716 Dnm1 dynamin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:27363778 1552716 Dnm1 dynamin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:20059951 1552716 Dnm1 dynamin 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20200310 MGI PMID:17463283 1552716 Dnm1 dynamin 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:25417109 1552716 Dnm1 dynamin 1 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20200310 MGI PMID:20700442 1552716 Dnm1 dynamin 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:17463283 1552716 Dnm1 dynamin 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:17463283 1552716 Dnm1 dynamin 1 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1552716 Dnm1 dynamin 1 gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20200310 MGI PMID:21689597 1552716 Dnm1 dynamin 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20200310 MGI PMID:20700442 1552716 Dnm1 dynamin 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:17463283 1552716 Dnm1 dynamin 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:21689597 1552716 Dnm1 dynamin 1 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20200310 MGI PMID:17463283 1552716 Dnm1 dynamin 1 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20200310 MGI PMID:21689597 1552716 Dnm1 dynamin 1 gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20200310 MGI PMID:17463283 1552716 Dnm1 dynamin 1 gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20200310 MGI PMID:21689597 1552716 Dnm1 dynamin 1 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20200310 MGI PMID:17463283 1552716 Dnm1 dynamin 1 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20200310 MGI PMID:21689597 1552716 Dnm1 dynamin 1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20200310 MGI PMID:27363778 1552716 Dnm1 dynamin 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:20059951 1552716 Dnm1 dynamin 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:25417109 1552716 Dnm1 dynamin 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20200310 MGI PMID:20700442 1552716 Dnm1 dynamin 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20200310 MGI PMID:21689597 1552716 Dnm1 dynamin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17463283 1552716 Dnm1 dynamin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20700442 1552716 Dnm1 dynamin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21689597 1552716 Dnm1 dynamin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552716 Dnm1 dynamin 1 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20200310 MGI PMID:21689597 1552716 Dnm1 dynamin 1 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20200310 MGI PMID:20700442 1552716 Dnm1 dynamin 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:20700442 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:11961557 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:14597717 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:14597717 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0000921 demyelination IAGP N RGD:5509061 20200310 MGI PMID:12707359 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:19088190 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:21494554 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:12707359 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:18493980 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20200310 MGI PMID:12707359 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:14597717 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20200310 MGI PMID:14597717 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200310 MGI PMID:12707359 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20200310 MGI PMID:11961557 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20200310 MGI PMID:16148148 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:14597717 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20200310 MGI PMID:12707359 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20200310 MGI PMID:14597717 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20200310 MGI PMID:14597717 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0008471 abnormal spleen primary B follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:14597717 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20200310 MGI PMID:12707359 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20200310 MGI PMID:14597717 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:12707359 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20200310 MGI PMID:21494554 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20200310 MGI PMID:10708458 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20200310 MGI PMID:21494554 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:18493980 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20200310 MGI PMID:12707359 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20200310 MGI PMID:14597717 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20200310 MGI PMID:14597717 1552719 Ifnb1 interferon beta 1, fibroblast gene MP:0020928 increased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:10708458 1552725 Dnah8 dynein, axonemal, heavy chain 8 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20201210 MGI PMID:32619401 1552725 Dnah8 dynein, axonemal, heavy chain 8 gene MP:0001925 male infertility IAGP N RGD:5509061 20201210 MGI PMID:32619401 1552725 Dnah8 dynein, axonemal, heavy chain 8 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20201210 MGI PMID:32619401 1552725 Dnah8 dynein, axonemal, heavy chain 8 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20201210 MGI PMID:32619401 1552725 Dnah8 dynein, axonemal, heavy chain 8 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20201210 MGI PMID:32619401 1552725 Dnah8 dynein, axonemal, heavy chain 8 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20201210 MGI PMID:32619401 1552725 Dnah8 dynein, axonemal, heavy chain 8 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20201210 MGI PMID:32619401 1552725 Dnah8 dynein, axonemal, heavy chain 8 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20201210 MGI PMID:32619401 1552725 Dnah8 dynein, axonemal, heavy chain 8 gene MP:0014468 disorganized sperm mitochondrial sheath IAGP N RGD:5509061 20240613 MGI PMID:32619401 1552725 Dnah8 dynein, axonemal, heavy chain 8 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20201210 MGI PMID:32619401 1552725 Dnah8 dynein, axonemal, heavy chain 8 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20201210 MGI PMID:32619401 1552725 Dnah8 dynein, axonemal, heavy chain 8 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220811 MGI PMID:32619401 1552726 Dhh desert hedgehog gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141218 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:8805249 1552726 Dhh desert hedgehog gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:8805249 1552726 Dhh desert hedgehog gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:8805249 1552726 Dhh desert hedgehog gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8805249 1552726 Dhh desert hedgehog gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:8805249 1552726 Dhh desert hedgehog gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8805249 1552726 Dhh desert hedgehog gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:10482238 1552726 Dhh desert hedgehog gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:8805249 1552726 Dhh desert hedgehog gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:8805249 1552726 Dhh desert hedgehog gene MP:0006418 abnormal testis cord formation IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0006420 abnormal peritubular myoid cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0006421 decreased number of peritubular myoid cells IAGP N RGD:5509061 20141003 MGI PMID:11090455 1552726 Dhh desert hedgehog gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:8805249 1552731 Or10j5 olfactory receptor family 10 subfamily J member 5 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:12194868 1552731 Or10j5 olfactory receptor family 10 subfamily J member 5 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17537788 1552731 Or10j5 olfactory receptor family 10 subfamily J member 5 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:18353676 1552731 Or10j5 olfactory receptor family 10 subfamily J member 5 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:18353676 1552731 Or10j5 olfactory receptor family 10 subfamily J member 5 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12194868 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200514 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200514 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200514 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20221215 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20210520 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20211021 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0005387 immune system phenotype IEA N RGD:5509061 20210520 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20200514 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20210520 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20210520 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20210520 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20210520 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20210520 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0008725 increased heart atrium size IEA N RGD:5509061 20200514 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20210520 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20211021 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0013510 decreased CD4-negative NK T cell number IEA N RGD:5509061 20210520 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0013513 decreased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20210520 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0013649 decreased CD11b-high dendritic cell number IEA N RGD:5509061 20210520 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0013678 decreased Ly6C-positive NK T cell number IEA N RGD:5509061 20210520 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0013679 increased Ly6C-positive NK T cell number IEA N RGD:5509061 20210520 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0013691 decreased CD5-positive Ly6C-positive T cell number IEA N RGD:5509061 20210520 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20210520 MGI 1552732 Nub1 negative regulator of ubiquitin-like proteins 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:15486564 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:15486564 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15486564 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15486564 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17554336 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18159219 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22948941 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15486564 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20150129 MGI PMID:24504341 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:15486564 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:9814708 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21474102 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22020437 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:15486564 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9814708 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:15486564 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20150129 MGI PMID:24504341 1552733 Pou5f1 POU domain, class 5, transcription factor 1 gene MP:0011411 abnormal gonadal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:15486564 1552735 Krt9 keratin 9 gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20141003 MGI PMID:23962810 1552735 Krt9 keratin 9 gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:23962810 1552735 Krt9 keratin 9 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:23962810 1552735 Krt9 keratin 9 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:23962810 1552735 Krt9 keratin 9 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:23962810 1552735 Krt9 keratin 9 gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20141003 MGI PMID:23962810 1552735 Krt9 keratin 9 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:23962810 1552735 Krt9 keratin 9 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:23962810 1552735 Krt9 keratin 9 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:23962810 1552735 Krt9 keratin 9 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:23962810 1552735 Krt9 keratin 9 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23962810 1552735 Krt9 keratin 9 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:23962810 1552735 Krt9 keratin 9 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20220519 MGI 1552735 Krt9 keratin 9 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23962810 1552735 Krt9 keratin 9 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:23962810 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:11239162 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:15265900 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:11239162 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20200310 MGI PMID:15265900 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:19401562 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15265900 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15265900 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:15265900 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20200310 MGI PMID:11239162 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:19401562 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20200310 MGI PMID:15265900 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:11239162 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:19401562 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:11239162 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:19401562 1552736 Grap2 GRB2-related adaptor protein 2 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:19401562 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15282321 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15282321 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:15282321 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15282321 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15282321 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:15282321 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:15282321 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:15282321 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15282321 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15282321 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:15282321 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20210121 MGI PMID:32876667 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15282321 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:15282321 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15282321 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15282321 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210121 MGI PMID:32876667 1552737 Ubr5 ubiquitin protein ligase E3 component n-recognin 5 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:15282321 1552738 Pdk1 pyruvate dehydrogenase kinase, isoenzyme 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220811 MGI 1552738 Pdk1 pyruvate dehydrogenase kinase, isoenzyme 1 gene MP:0001147 small testis IEA N RGD:5509061 20220811 MGI 1552738 Pdk1 pyruvate dehydrogenase kinase, isoenzyme 1 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20210610 MGI PMID:33773101 1552738 Pdk1 pyruvate dehydrogenase kinase, isoenzyme 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210610 MGI PMID:33773101 1552738 Pdk1 pyruvate dehydrogenase kinase, isoenzyme 1 gene MP:0005390 skeleton phenotype IAGP N RGD:5509061 20210610 MGI PMID:33773101 1552738 Pdk1 pyruvate dehydrogenase kinase, isoenzyme 1 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20210610 MGI PMID:33773101 1552738 Pdk1 pyruvate dehydrogenase kinase, isoenzyme 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20210610 MGI PMID:33773101 1552738 Pdk1 pyruvate dehydrogenase kinase, isoenzyme 1 gene MP:0010768 mortality/aging IAGP N RGD:5509061 20210610 MGI PMID:33773101 1552738 Pdk1 pyruvate dehydrogenase kinase, isoenzyme 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210610 MGI PMID:33773101 1552738 Pdk1 pyruvate dehydrogenase kinase, isoenzyme 1 gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20210610 MGI PMID:33773101 1552741 Rnase9 ribonuclease, RNase A family, 9 (non-active) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:24719258 1552741 Rnase9 ribonuclease, RNase A family, 9 (non-active) gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20160526 MGI PMID:24719258 1552741 Rnase9 ribonuclease, RNase A family, 9 (non-active) gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20160526 MGI PMID:24719258 1552742 Ipmk inositol polyphosphate multikinase gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20200310 MGI PMID:15939867 1552742 Ipmk inositol polyphosphate multikinase gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:15939867 1552742 Ipmk inositol polyphosphate multikinase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:15939867 1552742 Ipmk inositol polyphosphate multikinase gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20200310 MGI PMID:15939867 1552742 Ipmk inositol polyphosphate multikinase gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20200310 MGI PMID:15939867 1552742 Ipmk inositol polyphosphate multikinase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:15939867 1552742 Ipmk inositol polyphosphate multikinase gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20200310 MGI PMID:15939867 1552742 Ipmk inositol polyphosphate multikinase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15939867 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15103023 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17241289 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15118123 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19574394 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15118123 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:15103023 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:15103023 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15103023 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19574394 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:15118123 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15118123 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19574394 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15118123 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:17241289 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0002801 abnormal long-term object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:17241289 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15103023 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:15118123 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:19574394 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0003444 abnormal neurotransmitter uptake IAGP N RGD:5509061 20141003 MGI PMID:15118123 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:15118123 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:17241289 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15103023 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:15118123 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:15118123 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:15118123 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20230601 MGI 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15103023 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:15118123 1552743 Slc17a7 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 gene MP:0020340 abnormal inhibitory learning IAGP N RGD:5509061 20160915 MGI PMID:19574394 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230119 MGI 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16283624 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16109770 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:16109770 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16109770 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16109770 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16109770 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16283624 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16109770 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16283624 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:16109770 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16109770 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:10430909 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10430909 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12417405 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:23716689 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10430909 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12417405 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16109770 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16283624 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:10430909 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230119 MGI 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0003895 increased ectoderm apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10430909 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0003895 increased ectoderm apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12417405 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0003950 abnormal plasma membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:10430909 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0003954 abnormal Reichert's membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:10430909 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:23716689 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20230119 MGI 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:16109770 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:23716689 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:23716689 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23716689 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16109770 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10430909 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12417405 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1552745 Ugcg UDP-glucose ceramide glucosyltransferase gene MP:0011736 decreased urine ammonia level IAGP N RGD:5509061 20141003 MGI PMID:23716689 1552746 Gfm1 G elongation factor, mitochondrial 1 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20200310 MGI 1552746 Gfm1 G elongation factor, mitochondrial 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20210318 MGI PMID:33238133 1552746 Gfm1 G elongation factor, mitochondrial 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20210318 MGI PMID:33238133 1552746 Gfm1 G elongation factor, mitochondrial 1 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20210318 MGI PMID:33238133 1552746 Gfm1 G elongation factor, mitochondrial 1 gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20210318 MGI PMID:33238133 1552748 Mphosph10 M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1552748 Mphosph10 M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1552748 Mphosph10 M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 1552750 Masp1 MBL associated serine protease 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20240523 MGI 1552750 Masp1 MBL associated serine protease 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18424734 1552750 Masp1 MBL associated serine protease 1 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20240523 MGI 1552750 Masp1 MBL associated serine protease 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1552750 Masp1 MBL associated serine protease 1 gene MP:0002472 impaired complement alternative pathway IAGP N RGD:5509061 20141003 MGI PMID:21943708 1552750 Masp1 MBL associated serine protease 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1552750 Masp1 MBL associated serine protease 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1552750 Masp1 MBL associated serine protease 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20240523 MGI 1552750 Masp1 MBL associated serine protease 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18424734 1552750 Masp1 MBL associated serine protease 1 gene MP:0009062 impaired lectin complement pathway IAGP N RGD:5509061 20141003 MGI PMID:18424734 1552750 Masp1 MBL associated serine protease 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1552750 Masp1 MBL associated serine protease 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552750 Masp1 MBL associated serine protease 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1552754 Scly selenocysteine lyase gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:22487427 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0008600 decreased circulating interleukin-2 level IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552755 Nmt2 N-myristoyltransferase 2 gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20151203 MGI PMID:26423150 1552756 Ddx59 DEAD box helicase 59 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191205 MGI 1552756 Ddx59 DEAD box helicase 59 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191205 MGI 1552756 Ddx59 DEAD box helicase 59 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191205 MGI 1552756 Ddx59 DEAD box helicase 59 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1552756 Ddx59 DEAD box helicase 59 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20170504 MGI 1552756 Ddx59 DEAD box helicase 59 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191205 MGI 1552756 Ddx59 DEAD box helicase 59 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191205 MGI 1552756 Ddx59 DEAD box helicase 59 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1552756 Ddx59 DEAD box helicase 59 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552756 Ddx59 DEAD box helicase 59 gene MP:0012724 absent head fold IEA N RGD:5509061 20191205 MGI 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15887119 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15887119 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15887119 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0003978 decreased circulating carnitine level IAGP N RGD:5509061 20141003 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20141003 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15887119 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:11390422 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:15887119 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:15887119 1552757 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:15887119 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:14729950 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:14729950 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14729950 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:17140559 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0001288 abnormal lens induction IAGP N RGD:5509061 20141003 MGI PMID:17140559 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:17140559 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17140559 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:17140559 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:17140559 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:14729950 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20876643 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14729950 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20876643 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0001717 absent ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:20876643 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:20876643 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:14729950 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0003817 abnormal pituitary diverticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:17140559 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:20876643 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:17140559 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:14729950 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0006293 absent nasal placodes IAGP N RGD:5509061 20141003 MGI PMID:17140559 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0008533 abnormal anterior visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:20876643 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:20876643 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14729950 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14729950 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20876643 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14729950 1552758 Pou2f1 POU domain, class 2, transcription factor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14729950 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20200310 MGI PMID:25217574 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20200310 MGI PMID:25217574 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20200310 MGI PMID:25822906 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20200310 MGI PMID:25819842 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:23863714 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0001967 deafness IAGP N RGD:5509061 20200310 MGI PMID:25217574 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0001967 deafness IAGP N RGD:5509061 20200310 MGI PMID:25819842 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20200310 MGI PMID:25217574 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0002630 abnormal endocochlear potential IAGP N RGD:5509061 20200310 MGI PMID:25217574 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0003151 absent tunnel of Corti IAGP N RGD:5509061 20200310 MGI PMID:25819842 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:25217574 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:25822906 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:25217574 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:25819842 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:25822906 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20200310 MGI PMID:25217574 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20200310 MGI PMID:25822906 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20200310 MGI PMID:25217574 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20200310 MGI PMID:25822906 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:23863714 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20200310 MGI 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:25217574 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:25819842 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:25822906 1552760 Ildr1 immunoglobulin-like domain containing receptor 1 gene MP:0013808 abnormal tunnel of Corti morphology IAGP N RGD:5509061 20200310 MGI PMID:25819842 1552761 Msrb3 methionine sulfoxide reductase B3 gene MP:0001967 deafness IAGP N RGD:5509061 20200310 MGI PMID:24191262 1552761 Msrb3 methionine sulfoxide reductase B3 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:24191262 1552761 Msrb3 methionine sulfoxide reductase B3 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:24191262 1552761 Msrb3 methionine sulfoxide reductase B3 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20200310 MGI PMID:24191262 1552761 Msrb3 methionine sulfoxide reductase B3 gene MP:0004530 absent outer hair cell stereocilia IAGP N RGD:5509061 20200310 MGI PMID:24191262 1552761 Msrb3 methionine sulfoxide reductase B3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:24191262 1552761 Msrb3 methionine sulfoxide reductase B3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:24191262 1552763 Dmxl1 Dmx-like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1552765 Itgb6 integrin beta 6 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:8666675 1552765 Itgb6 integrin beta 6 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:8666675 1552765 Itgb6 integrin beta 6 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12634787 1552765 Itgb6 integrin beta 6 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:8666675 1552765 Itgb6 integrin beta 6 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:9761761 1552765 Itgb6 integrin beta 6 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1552765 Itgb6 integrin beta 6 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1552765 Itgb6 integrin beta 6 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:8666675 1552765 Itgb6 integrin beta 6 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:12634787 1552765 Itgb6 integrin beta 6 gene MP:0001262 decreased body weight IEA N RGD:5509061 20230119 MGI 1552765 Itgb6 integrin beta 6 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230119 MGI 1552765 Itgb6 integrin beta 6 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17353357 1552765 Itgb6 integrin beta 6 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12634787 1552765 Itgb6 integrin beta 6 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:12634787 1552765 Itgb6 integrin beta 6 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1552765 Itgb6 integrin beta 6 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1552765 Itgb6 integrin beta 6 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230119 MGI 1552765 Itgb6 integrin beta 6 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 1552765 Itgb6 integrin beta 6 gene MP:0002311 abnormal inspiratory capacity IEA N RGD:5509061 20240627 MGI 1552765 Itgb6 integrin beta 6 gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:8666675 1552765 Itgb6 integrin beta 6 gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:9761761 1552765 Itgb6 integrin beta 6 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1552765 Itgb6 integrin beta 6 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:14507636 1552765 Itgb6 integrin beta 6 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:14507636 1552765 Itgb6 integrin beta 6 gene MP:0008118 absent Langerhans cell IAGP N RGD:5509061 20141003 MGI PMID:17353357 1552765 Itgb6 integrin beta 6 gene MP:0008119 decreased Langerhans cell number IAGP N RGD:5509061 20141003 MGI PMID:17353357 1552765 Itgb6 integrin beta 6 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20240523 MGI 1552765 Itgb6 integrin beta 6 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20230119 MGI 1552765 Itgb6 integrin beta 6 gene MP:0010895 increased lung compliance IEA N RGD:5509061 20230119 MGI 1552765 Itgb6 integrin beta 6 gene MP:0011045 decreased lung elastance IEA N RGD:5509061 20230119 MGI 1552765 Itgb6 integrin beta 6 gene MP:0011048 decreased lung tissue damping IEA N RGD:5509061 20230119 MGI 1552765 Itgb6 integrin beta 6 gene MP:0013129 abnormal tooth color IEA N RGD:5509061 20230119 MGI 1552765 Itgb6 integrin beta 6 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230119 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210520 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0002188 small heart IEA N RGD:5509061 20210826 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20201022 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20201022 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210520 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1552768 Nucb1 nucleobindin 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1552771 Tmem14a transmembrane protein 14A gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1552773 Ubac1 ubiquitin associated domain containing 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1552773 Ubac1 ubiquitin associated domain containing 1 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1552773 Ubac1 ubiquitin associated domain containing 1 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1552773 Ubac1 ubiquitin associated domain containing 1 gene MP:0005287 narrow eye opening IEA N RGD:5509061 20201022 MGI 1552773 Ubac1 ubiquitin associated domain containing 1 gene MP:0005542 cornea vascularization IEA N RGD:5509061 20201022 MGI 1552773 Ubac1 ubiquitin associated domain containing 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1552773 Ubac1 ubiquitin associated domain containing 1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20220811 MGI 1552773 Ubac1 ubiquitin associated domain containing 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1552776 Ldhc lactate dehydrogenase C gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:18367675 1552776 Ldhc lactate dehydrogenase C gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:18367675 1552776 Ldhc lactate dehydrogenase C gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18367675 1552776 Ldhc lactate dehydrogenase C gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18367675 1552776 Ldhc lactate dehydrogenase C gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:18367675 1552776 Ldhc lactate dehydrogenase C gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20141003 MGI PMID:18367675 1552777 Tspyl1 testis-specific protein, Y-encoded-like 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1552777 Tspyl1 testis-specific protein, Y-encoded-like 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1552777 Tspyl1 testis-specific protein, Y-encoded-like 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1552777 Tspyl1 testis-specific protein, Y-encoded-like 1 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20201022 MGI 1552777 Tspyl1 testis-specific protein, Y-encoded-like 1 gene MP:0005655 increased aggression IEA N RGD:5509061 20240523 MGI 1552777 Tspyl1 testis-specific protein, Y-encoded-like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552780 Eva1c eva-1 homolog C gene MP:0002638 abnormal pupillary reflex IEA N RGD:5509061 20170323 MGI 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20210128 MGI 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18187333 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:17535435 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15799973 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18187333 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:24075852 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18187333 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:18187333 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:17560790 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:15799973 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:15721235 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:17560790 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:15799973 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:24075852 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20150319 MGI PMID:23019375 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:15721235 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:15799973 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:18187333 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20150319 MGI PMID:23019375 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20150319 MGI PMID:23019375 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:17535435 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0003444 abnormal neurotransmitter uptake IAGP N RGD:5509061 20141003 MGI PMID:15721235 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20150319 MGI PMID:23019375 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20150319 MGI PMID:23019375 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:15721235 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:15721235 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20180215 MGI PMID:28360124 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0008830 abnormal nucleolus morphology IAGP N RGD:5509061 20180215 MGI PMID:28360124 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15784737 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15784737 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:18187333 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20150319 MGI PMID:23019375 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:24075852 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:17766438 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20141003 MGI PMID:17766438 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17560790 1552781 Park7 Parkinson disease (autosomal recessive, early onset) 7 gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20150319 MGI PMID:23019375 1552783 Ubb ubiquitin B gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:18299572 1552783 Ubb ubiquitin B gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:18299572 1552783 Ubb ubiquitin B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18299572 1552783 Ubb ubiquitin B gene MP:0001326 retina degeneration IAGP N RGD:5509061 20191107 MGI PMID:30935687 1552783 Ubb ubiquitin B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18299572 1552783 Ubb ubiquitin B gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:18299572 1552783 Ubb ubiquitin B gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:18299572 1552783 Ubb ubiquitin B gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18299572 1552783 Ubb ubiquitin B gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18299572 1552783 Ubb ubiquitin B gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20191107 MGI PMID:30935687 1552783 Ubb ubiquitin B gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20191107 MGI PMID:30935687 1552783 Ubb ubiquitin B gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20191107 MGI PMID:30935687 1552783 Ubb ubiquitin B gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0009375 thin zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18299572 1552783 Ubb ubiquitin B gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:18299572 1552783 Ubb ubiquitin B gene MP:0013600 testis degeneration IAGP N RGD:5509061 20150312 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0014447 impaired spindle assembly in female meiosis IAGP N RGD:5509061 20240509 MGI PMID:18070917 1552783 Ubb ubiquitin B gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220630 MGI PMID:18070917 1552784 Rhcg Rhesus blood group-associated C glycoprotein gene MP:0000525 renal tubular acidosis IAGP N RGD:5509061 20141003 MGI PMID:19020613 1552784 Rhcg Rhesus blood group-associated C glycoprotein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19020613 1552784 Rhcg Rhesus blood group-associated C glycoprotein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:19020613 1552784 Rhcg Rhesus blood group-associated C glycoprotein gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:19020613 1552784 Rhcg Rhesus blood group-associated C glycoprotein gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:23281477 1552784 Rhcg Rhesus blood group-associated C glycoprotein gene MP:0003031 acidosis IAGP N RGD:5509061 20141003 MGI PMID:19020613 1552784 Rhcg Rhesus blood group-associated C glycoprotein gene MP:0003031 acidosis IAGP N RGD:5509061 20141003 MGI PMID:23281477 1552784 Rhcg Rhesus blood group-associated C glycoprotein gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:23281477 1552784 Rhcg Rhesus blood group-associated C glycoprotein gene MP:0005628 decreased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:19020613 1552784 Rhcg Rhesus blood group-associated C glycoprotein gene MP:0009349 increased urine pH IAGP N RGD:5509061 20141003 MGI PMID:19020613 1552784 Rhcg Rhesus blood group-associated C glycoprotein gene MP:0009349 increased urine pH IAGP N RGD:5509061 20141003 MGI PMID:23281477 1552784 Rhcg Rhesus blood group-associated C glycoprotein gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23281477 1552784 Rhcg Rhesus blood group-associated C glycoprotein gene MP:0011736 decreased urine ammonia level IAGP N RGD:5509061 20141003 MGI PMID:19020613 1552784 Rhcg Rhesus blood group-associated C glycoprotein gene MP:0011736 decreased urine ammonia level IAGP N RGD:5509061 20141003 MGI PMID:23281477 1552785 Panx3 pannexin 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20160825 MGI PMID:26138248 1552785 Panx3 pannexin 3 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20160825 MGI PMID:26138248 1552785 Panx3 pannexin 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1552785 Panx3 pannexin 3 gene MP:0013304 osteophytes IAGP N RGD:5509061 20160825 MGI PMID:26138248 1552786 Aox4 aldehyde oxidase 4 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20200310 MGI PMID:18981221 1552786 Aox4 aldehyde oxidase 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18981221 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000071 axial skeleton hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20160505 MGI PMID:25126760 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:19056490 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:19715689 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:19715689 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17986259 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:17986259 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20160505 MGI PMID:25126760 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:17986259 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17986259 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17986259 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25126760 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:17986259 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0004266 pale placenta IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0004447 small basioccipital bone IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20160505 MGI PMID:25126760 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0004572 fusion of basioccipital and basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20160505 MGI PMID:25126760 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19715689 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0005352 small cranium IAGP N RGD:5509061 20160505 MGI PMID:25126760 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0009384 cardiac valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0009912 decreased hyoid bone size IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0010941 abnormal foramen magnum morphology IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:19715689 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0010987 abnormal nephrogenic mesenchyme morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19715689 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17986259 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0011177 abnormal erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0011292 absent nephron IAGP N RGD:5509061 20141003 MGI PMID:19715689 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0011364 abnormal metanephros morphology IAGP N RGD:5509061 20141003 MGI PMID:19715689 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0011366 absent metanephros IAGP N RGD:5509061 20141003 MGI PMID:19715689 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0011366 absent metanephros IAGP N RGD:5509061 20160505 MGI PMID:25126760 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19715689 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19715689 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0011527 disorganized placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20141003 MGI PMID:17986259 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0012514 pectus excavatum IAGP N RGD:5509061 20141003 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0030279 thin neurocranium IAGP N RGD:5509061 20171102 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0030867 small thyroid cartilage IAGP N RGD:5509061 20181101 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0030872 small cricoid cartilage IAGP N RGD:5509061 20181101 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0031574 thick atrioventricular valve IAGP N RGD:5509061 20240125 MGI PMID:19383940 1552790 Fgfrl1 fibroblast growth factor receptor-like 1 gene MP:0031584 thick semilunar valve IAGP N RGD:5509061 20240125 MGI PMID:19383940 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:24509076 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:20643340 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230601 MGI 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20643340 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:24509076 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:20643340 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:24509076 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:24509076 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20643340 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:24509076 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:24509076 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:20643340 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20643340 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:24509076 1552792 Cxcl5 C-X-C motif chemokine ligand 5 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:20643340 1552794 Cnih2 cornichon family AMPA receptor auxiliary protein 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1552794 Cnih2 cornichon family AMPA receptor auxiliary protein 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20230601 MGI 1552794 Cnih2 cornichon family AMPA receptor auxiliary protein 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1552794 Cnih2 cornichon family AMPA receptor auxiliary protein 2 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20201022 MGI 1552794 Cnih2 cornichon family AMPA receptor auxiliary protein 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20200310 MGI PMID:23522044 1552794 Cnih2 cornichon family AMPA receptor auxiliary protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:23522044 1552794 Cnih2 cornichon family AMPA receptor auxiliary protein 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1552794 Cnih2 cornichon family AMPA receptor auxiliary protein 2 gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20200310 MGI PMID:23522044 1552794 Cnih2 cornichon family AMPA receptor auxiliary protein 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1552794 Cnih2 cornichon family AMPA receptor auxiliary protein 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1552794 Cnih2 cornichon family AMPA receptor auxiliary protein 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:23522044 1552794 Cnih2 cornichon family AMPA receptor auxiliary protein 2 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20200310 MGI PMID:23522044 1552798 Brinp2 bone morphogenic protein/retinoic acid inducible neural-specific 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1552798 Brinp2 bone morphogenic protein/retinoic acid inducible neural-specific 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20240523 MGI 1552798 Brinp2 bone morphogenic protein/retinoic acid inducible neural-specific 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1552800 Reg3g regenerating islet-derived 3 gamma gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20150108 MGI 1552800 Reg3g regenerating islet-derived 3 gamma gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20150108 MGI 1552800 Reg3g regenerating islet-derived 3 gamma gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:21998396 1552800 Reg3g regenerating islet-derived 3 gamma gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:21998396 1552800 Reg3g regenerating islet-derived 3 gamma gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20150108 MGI 1552800 Reg3g regenerating islet-derived 3 gamma gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:21998396 1552800 Reg3g regenerating islet-derived 3 gamma gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:21998396 1552800 Reg3g regenerating islet-derived 3 gamma gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20141003 MGI PMID:21998396 1552800 Reg3g regenerating islet-derived 3 gamma gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:26329040 1552802 Syt17 synaptotagmin XVII gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20231207 MGI 1552802 Syt17 synaptotagmin XVII gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1552802 Syt17 synaptotagmin XVII gene MP:0002764 short tibia IEA N RGD:5509061 20200310 MGI 1552802 Syt17 synaptotagmin XVII gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20231207 MGI 1552802 Syt17 synaptotagmin XVII gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1552802 Syt17 synaptotagmin XVII gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 1552802 Syt17 synaptotagmin XVII gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20231207 MGI 1552802 Syt17 synaptotagmin XVII gene MP:0005573 increased pulmonary respiratory rate IEA N RGD:5509061 20210128 MGI 1552802 Syt17 synaptotagmin XVII gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:15252120 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:12609501 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:12609501 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:15252120 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:12609501 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:12609501 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:9732288 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10485893 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9732288 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:15252120 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9732288 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15252120 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9732288 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:15252120 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15252120 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12609501 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9732288 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19884661 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:12609501 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:9732288 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:9732288 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:9732288 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:12609501 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12609501 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12609501 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:12609501 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:12609501 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9732288 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15252120 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15252120 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:12609501 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:12609501 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19884661 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12609501 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0010052 increased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19884661 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19884661 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:10485893 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:12609501 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:9732288 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15252120 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0012059 thick diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:9732288 1552804 Sgcg sarcoglycan, gamma (dystrophin-associated glycoprotein) gene MP:0031192 coronary artery spasm IAGP N RGD:5509061 20201119 MGI PMID:14982859 1552805 Serping1 serine (or cysteine) peptidase inhibitor, clade G, member 1 gene MP:0000774 decreased brain size IEA N RGD:5509061 20210520 MGI 1552805 Serping1 serine (or cysteine) peptidase inhibitor, clade G, member 1 gene MP:0001304 cataract IEA N RGD:5509061 20210826 MGI 1552805 Serping1 serine (or cysteine) peptidase inhibitor, clade G, member 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1552805 Serping1 serine (or cysteine) peptidase inhibitor, clade G, member 1 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210520 MGI 1552805 Serping1 serine (or cysteine) peptidase inhibitor, clade G, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11956243 1552805 Serping1 serine (or cysteine) peptidase inhibitor, clade G, member 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1552805 Serping1 serine (or cysteine) peptidase inhibitor, clade G, member 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1552805 Serping1 serine (or cysteine) peptidase inhibitor, clade G, member 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1552805 Serping1 serine (or cysteine) peptidase inhibitor, clade G, member 1 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:11956243 1552806 Nubpl nucleotide binding protein-like gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20200310 MGI PMID:29539633 1552806 Nubpl nucleotide binding protein-like gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20200310 MGI PMID:29539633 1552806 Nubpl nucleotide binding protein-like gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20200310 MGI PMID:29539633 1552806 Nubpl nucleotide binding protein-like gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29539633 1552806 Nubpl nucleotide binding protein-like gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20230413 MGI PMID:36280881 1552806 Nubpl nucleotide binding protein-like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552806 Nubpl nucleotide binding protein-like gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170105 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0001147 small testis IEA N RGD:5509061 20170105 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20181227 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20181227 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20210128 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1552812 Gpld1 glycosylphosphatidylinositol specific phospholipase D1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20210715 MGI PMID:33899734 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20210715 MGI PMID:33899734 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20210715 MGI PMID:33899734 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20210715 MGI PMID:33899734 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:12556505 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160211 MGI PMID:24835669 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20160211 MGI PMID:24835669 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12556505 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12556505 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160211 MGI PMID:24835669 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0002892 decreased superior colliculus size IAGP N RGD:5509061 20210715 MGI PMID:33899734 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20210715 MGI PMID:33899734 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20210715 MGI PMID:33899734 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12556505 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:12556505 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:12556505 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20210715 MGI PMID:33899734 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20210715 MGI PMID:33899734 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20210715 MGI PMID:33899734 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0009960 abnormal cerebellum anterior lobe morphology IAGP N RGD:5509061 20210715 MGI PMID:33899734 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160211 MGI PMID:24835669 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12556505 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20210715 MGI PMID:33899734 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0011209 absent extraembryonic coelom IAGP N RGD:5509061 20141003 MGI PMID:12556505 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:12556505 1552813 Pelo pelota mRNA surveillance and ribosome rescue factor gene MP:0020393 increased neuronal precursor proliferation IAGP N RGD:5509061 20210715 MGI PMID:33899734 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21750680 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20201022 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20170105 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20201022 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:21750680 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0000566 synostosis IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0000576 clubfoot IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21750680 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230601 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20170105 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21750680 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20141003 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20170105 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0002546 mydriasis IEA N RGD:5509061 20230601 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230601 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0003757 high palate IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20201022 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20201022 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0004642 fused metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21750680 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0005287 narrow eye opening IEA N RGD:5509061 20230601 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0005430 absent fibula IAGP N RGD:5509061 20141003 MGI PMID:21750680 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21750680 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20230601 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20230601 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0009874 abnormal interdigital cell death IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230601 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0010714 iris coloboma IAGP N RGD:5509061 20141003 MGI PMID:21750680 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0010715 retina coloboma IAGP N RGD:5509061 20141003 MGI PMID:21750680 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0010772 abnormal pollex morphology IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21194678 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21750680 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0011496 abnormal head size IEA N RGD:5509061 20201022 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 1552814 Smoc1 SPARC related modular calcium binding 1 gene MP:0031291 pes valgus IAGP N RGD:5509061 20211014 MGI PMID:21194678 1552815 Miox myo-inositol oxygenase gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20200310 MGI PMID:27895157 1552815 Miox myo-inositol oxygenase gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20200310 MGI PMID:27895157 1552816 Krt33b keratin 33B gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1552816 Krt33b keratin 33B gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1552816 Krt33b keratin 33B gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1552816 Krt33b keratin 33B gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1552816 Krt33b keratin 33B gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1552816 Krt33b keratin 33B gene MP:0003604 single kidney IEA N RGD:5509061 20210128 MGI 1552816 Krt33b keratin 33B gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1552819 Aurka aurora kinase A gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1552819 Aurka aurora kinase A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:19075002 1552819 Aurka aurora kinase A gene MP:0001147 small testis IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:18345035 1552819 Aurka aurora kinase A gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:18801727 1552819 Aurka aurora kinase A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0001926 female infertility IAGP N RGD:5509061 20220616 MGI PMID:33901174 1552819 Aurka aurora kinase A gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:18801727 1552819 Aurka aurora kinase A gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20220616 MGI PMID:33901174 1552819 Aurka aurora kinase A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20200310 MGI PMID:18345035 1552819 Aurka aurora kinase A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:18345035 1552819 Aurka aurora kinase A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:19075002 1552819 Aurka aurora kinase A gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20200310 MGI PMID:19075002 1552819 Aurka aurora kinase A gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1552819 Aurka aurora kinase A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:18345035 1552819 Aurka aurora kinase A gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20200310 MGI PMID:19075002 1552819 Aurka aurora kinase A gene MP:0004024 aneuploidy IAGP N RGD:5509061 20200310 MGI PMID:18801727 1552819 Aurka aurora kinase A gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200310 MGI PMID:18345035 1552819 Aurka aurora kinase A gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200310 MGI PMID:18801727 1552819 Aurka aurora kinase A gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200310 MGI PMID:19075002 1552819 Aurka aurora kinase A gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18801727 1552819 Aurka aurora kinase A gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20200310 MGI PMID:19075002 1552819 Aurka aurora kinase A gene MP:0004806 absent germ cells IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20200310 MGI PMID:18345035 1552819 Aurka aurora kinase A gene MP:0005159 azoospermia IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:19075002 1552819 Aurka aurora kinase A gene MP:0006204 embryonic lethality before implantation IAGP N RGD:5509061 20200310 MGI PMID:18801727 1552819 Aurka aurora kinase A gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18801727 1552819 Aurka aurora kinase A gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20200310 MGI PMID:18801727 1552819 Aurka aurora kinase A gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20200310 MGI PMID:18345035 1552819 Aurka aurora kinase A gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20200310 MGI PMID:18801727 1552819 Aurka aurora kinase A gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20200310 MGI PMID:19075002 1552819 Aurka aurora kinase A gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20220616 MGI PMID:33901174 1552819 Aurka aurora kinase A gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20200310 MGI PMID:19075002 1552819 Aurka aurora kinase A gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0009839 multiflagellated sperm IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18801727 1552819 Aurka aurora kinase A gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20220616 MGI PMID:33901174 1552819 Aurka aurora kinase A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18345035 1552819 Aurka aurora kinase A gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19075002 1552819 Aurka aurora kinase A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552819 Aurka aurora kinase A gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0012121 sclerocornea IEA N RGD:5509061 20200310 MGI 1552819 Aurka aurora kinase A gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18801727 1552819 Aurka aurora kinase A gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1552819 Aurka aurora kinase A gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1552819 Aurka aurora kinase A gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220707 MGI PMID:34518881 1552819 Aurka aurora kinase A gene MP:0031427 increased sperm progressive motility IAGP N RGD:5509061 20220714 MGI PMID:34518881 1552820 Wsb2 WD repeat and SOCS box-containing 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 1552820 Wsb2 WD repeat and SOCS box-containing 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210520 MGI 1552820 Wsb2 WD repeat and SOCS box-containing 2 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1552820 Wsb2 WD repeat and SOCS box-containing 2 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1552820 Wsb2 WD repeat and SOCS box-containing 2 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20160421 MGI 1552820 Wsb2 WD repeat and SOCS box-containing 2 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20160811 MGI 1552820 Wsb2 WD repeat and SOCS box-containing 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20170105 MGI 1552820 Wsb2 WD repeat and SOCS box-containing 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1552820 Wsb2 WD repeat and SOCS box-containing 2 gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20211021 MGI 1552820 Wsb2 WD repeat and SOCS box-containing 2 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20170105 MGI 1552820 Wsb2 WD repeat and SOCS box-containing 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1552820 Wsb2 WD repeat and SOCS box-containing 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20170105 MGI 1552820 Wsb2 WD repeat and SOCS box-containing 2 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20160421 MGI 1552820 Wsb2 WD repeat and SOCS box-containing 2 gene MP:0011940 decreased food intake IEA N RGD:5509061 20160421 MGI 1552820 Wsb2 WD repeat and SOCS box-containing 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20170105 MGI 1552821 Golt1b golgi transport 1B gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20210128 MGI 1552821 Golt1b golgi transport 1B gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1552821 Golt1b golgi transport 1B gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1552821 Golt1b golgi transport 1B gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1552821 Golt1b golgi transport 1B gene MP:0003393 decreased cardiac output IEA N RGD:5509061 20200310 MGI 1552821 Golt1b golgi transport 1B gene MP:0010052 increased grip strength IEA N RGD:5509061 20200310 MGI 1552821 Golt1b golgi transport 1B gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20240523 MGI 1552821 Golt1b golgi transport 1B gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210128 MGI 1552822 Fam210a family with sequence similarity 210, member A gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552822 Fam210a family with sequence similarity 210, member A gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552822 Fam210a family with sequence similarity 210, member A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552822 Fam210a family with sequence similarity 210, member A gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1552822 Fam210a family with sequence similarity 210, member A gene MP:0002083 premature death IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552822 Fam210a family with sequence similarity 210, member A gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552822 Fam210a family with sequence similarity 210, member A gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20170105 MGI 1552822 Fam210a family with sequence similarity 210, member A gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552822 Fam210a family with sequence similarity 210, member A gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552822 Fam210a family with sequence similarity 210, member A gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552822 Fam210a family with sequence similarity 210, member A gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552822 Fam210a family with sequence similarity 210, member A gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552822 Fam210a family with sequence similarity 210, member A gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552822 Fam210a family with sequence similarity 210, member A gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552822 Fam210a family with sequence similarity 210, member A gene MP:0010965 decreased compact bone volume IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552822 Fam210a family with sequence similarity 210, member A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552822 Fam210a family with sequence similarity 210, member A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1552822 Fam210a family with sequence similarity 210, member A gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1552822 Fam210a family with sequence similarity 210, member A gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1552822 Fam210a family with sequence similarity 210, member A gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552822 Fam210a family with sequence similarity 210, member A gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20180614 MGI PMID:29618611 1552823 Or10a2 olfactory receptor family 10 subfamily A member 2 gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15186781 1552824 Ankrd46 ankyrin repeat domain 46 gene MP:0001265 decreased body size IEA N RGD:5509061 20231207 MGI 1552825 Vcpip1 valosin containing protein (p97)/p47 complex interacting protein 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20210422 MGI PMID:32649882 1552825 Vcpip1 valosin containing protein (p97)/p47 complex interacting protein 1 gene MP:0000162 lordosis IAGP N RGD:5509061 20210422 MGI PMID:32649882 1552825 Vcpip1 valosin containing protein (p97)/p47 complex interacting protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210422 MGI PMID:32649882 1552825 Vcpip1 valosin containing protein (p97)/p47 complex interacting protein 1 gene MP:0001304 cataract IAGP N RGD:5509061 20210422 MGI PMID:32649882 1552825 Vcpip1 valosin containing protein (p97)/p47 complex interacting protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20210422 MGI PMID:32649882 1552825 Vcpip1 valosin containing protein (p97)/p47 complex interacting protein 1 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20210422 MGI PMID:32649882 1552825 Vcpip1 valosin containing protein (p97)/p47 complex interacting protein 1 gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20210422 MGI PMID:32649882 1552825 Vcpip1 valosin containing protein (p97)/p47 complex interacting protein 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20210422 MGI PMID:32649882 1552825 Vcpip1 valosin containing protein (p97)/p47 complex interacting protein 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20210422 MGI PMID:32649882 1552825 Vcpip1 valosin containing protein (p97)/p47 complex interacting protein 1 gene MP:0014040 increased cellular sensitivity to DNA damaging agents IAGP N RGD:5509061 20210422 MGI PMID:32649882 1552828 Nasp nuclear autoantigenic sperm protein (histone-binding) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16728391 1552828 Nasp nuclear autoantigenic sperm protein (histone-binding) gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16728391 1552828 Nasp nuclear autoantigenic sperm protein (histone-binding) gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16728391 1552829 Ces2a carboxylesterase 2A gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0001260 increased body weight IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0001860 liver inflammation IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0002981 increased liver weight IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0005331 insulin resistance IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0014170 increased brown adipose tissue mass IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0020582 increased ceramide level IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552829 Ces2a carboxylesterase 2A gene MP:0031269 increased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240912 MGI PMID:37059417 1552832 Nme8 NME/NM23 family member 8 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23707457 1552832 Nme8 NME/NM23 family member 8 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23707457 1552832 Nme8 NME/NM23 family member 8 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:23707457 1552832 Nme8 NME/NM23 family member 8 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:23707457 1552832 Nme8 NME/NM23 family member 8 gene MP:0012582 increased peroxidase activity IAGP N RGD:5509061 20141003 MGI PMID:23707457 1552833 Zng1 Zn regulated GTPase metalloprotein activator 1 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20220714 MGI PMID:31862704 1552833 Zng1 Zn regulated GTPase metalloprotein activator 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20220714 MGI PMID:31862704 1552833 Zng1 Zn regulated GTPase metalloprotein activator 1 gene MP:0000536 hydroureter IAGP N RGD:5509061 20220714 MGI PMID:31862704 1552833 Zng1 Zn regulated GTPase metalloprotein activator 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20220714 MGI PMID:31862704 1552833 Zng1 Zn regulated GTPase metalloprotein activator 1 gene MP:0011425 abnormal kidney interstitium morphology IAGP N RGD:5509061 20220714 MGI PMID:31862704 1552833 Zng1 Zn regulated GTPase metalloprotein activator 1 gene MP:0011493 double ureter IAGP N RGD:5509061 20220714 MGI PMID:31862704 1552835 Drc3 dynein regulatory complex subunit 3 gene MP:0000440 domed cranium IAGP N RGD:5509061 20200310 MGI PMID:23968836 1552835 Drc3 dynein regulatory complex subunit 3 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200310 MGI PMID:23968836 1552835 Drc3 dynein regulatory complex subunit 3 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20200310 MGI PMID:23968836 1552835 Drc3 dynein regulatory complex subunit 3 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20200310 MGI PMID:23968836 1552835 Drc3 dynein regulatory complex subunit 3 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20200310 MGI PMID:23968836 1552835 Drc3 dynein regulatory complex subunit 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23968836 1552838 Morc3 microrchidia 3 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1552838 Morc3 microrchidia 3 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1552838 Morc3 microrchidia 3 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 1552838 Morc3 microrchidia 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1552838 Morc3 microrchidia 3 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1552838 Morc3 microrchidia 3 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1552838 Morc3 microrchidia 3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1552838 Morc3 microrchidia 3 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1552838 Morc3 microrchidia 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1552838 Morc3 microrchidia 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17332504 1552838 Morc3 microrchidia 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552838 Morc3 microrchidia 3 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 1552840 Eya2 EYA transcriptional coactivator and phosphatase 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1552840 Eya2 EYA transcriptional coactivator and phosphatase 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1552840 Eya2 EYA transcriptional coactivator and phosphatase 2 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1552840 Eya2 EYA transcriptional coactivator and phosphatase 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1552840 Eya2 EYA transcriptional coactivator and phosphatase 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20220428 MGI PMID:33715274 1552840 Eya2 EYA transcriptional coactivator and phosphatase 2 gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20220428 MGI PMID:33715274 1552840 Eya2 EYA transcriptional coactivator and phosphatase 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1552840 Eya2 EYA transcriptional coactivator and phosphatase 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20220428 MGI PMID:33715274 1552840 Eya2 EYA transcriptional coactivator and phosphatase 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20220428 MGI PMID:33715274 1552846 Emp2 epithelial membrane protein 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20171207 MGI PMID:28295343 1552846 Emp2 epithelial membrane protein 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20171207 MGI PMID:28295343 1552846 Emp2 epithelial membrane protein 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20171207 MGI PMID:28295343 1552846 Emp2 epithelial membrane protein 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20171207 MGI PMID:28295343 1552846 Emp2 epithelial membrane protein 2 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20171207 MGI PMID:28295343 1552846 Emp2 epithelial membrane protein 2 gene MP:0009394 increased uterine NK cell number IAGP N RGD:5509061 20171207 MGI PMID:28295343 1552846 Emp2 epithelial membrane protein 2 gene MP:0012529 abnormal decidua basalis morphology IAGP N RGD:5509061 20171207 MGI PMID:28295343 1552850 Pgpep1 pyroglutamyl-peptidase I gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20240523 MGI 1552850 Pgpep1 pyroglutamyl-peptidase I gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 1552850 Pgpep1 pyroglutamyl-peptidase I gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1552851 Cyp4f13 cytochrome P450, family 4, subfamily f, polypeptide 13 gene MP:0003192 increased cholesterol efflux IAGP N RGD:5509061 20201002 MGI PMID:31102955 1552851 Cyp4f13 cytochrome P450, family 4, subfamily f, polypeptide 13 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20201002 MGI PMID:31102955 1552851 Cyp4f13 cytochrome P450, family 4, subfamily f, polypeptide 13 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20201002 MGI PMID:31102955 1552851 Cyp4f13 cytochrome P450, family 4, subfamily f, polypeptide 13 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20201002 MGI PMID:31102955 1552853 Rims4 regulating synaptic membrane exocytosis 4 gene MP:0001262 decreased body weight IEA N RGD:5509061 20180222 MGI 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:2305264 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:7651535 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0000771 abnormal brain size IAGP N RGD:5509061 20141003 MGI PMID:7958830 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:7958830 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:10742101 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10742101 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7651535 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7958830 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10742101 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:2305264 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20190516 MGI PMID:28790031 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001924 infertility IEA N RGD:5509061 20111116 MGI 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12032866 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0002758 long tail IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:7958830 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0002772 brachypodia IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0002881 long hair IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0003415 priapism IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0003550 short perineum IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:12032866 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0005238 increased brain size IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:10742101 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0005352 small cranium IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:7958830 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:10742101 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:12032866 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:14794889 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0008526 decreased cranium width IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:2305264 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:7958830 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0009105 penis prolapse IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20190516 MGI PMID:28790031 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10742101 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10742101 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:7651535 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552855 Hmga2 high mobility group AT-hook 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220714 MGI PMID:34878116 1552857 Abca7 ATP-binding cassette, sub-family A member 7 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15550377 1552857 Abca7 ATP-binding cassette, sub-family A member 7 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15550377 1552857 Abca7 ATP-binding cassette, sub-family A member 7 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:15550377 1552857 Abca7 ATP-binding cassette, sub-family A member 7 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20211021 MGI 1552857 Abca7 ATP-binding cassette, sub-family A member 7 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15550377 1552857 Abca7 ATP-binding cassette, sub-family A member 7 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1552857 Abca7 ATP-binding cassette, sub-family A member 7 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20211021 MGI 1552857 Abca7 ATP-binding cassette, sub-family A member 7 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:14752163 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:21841778 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:14752163 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20200310 MGI PMID:21841778 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0001844 autoimmune response IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20200310 MGI PMID:21841778 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20200310 MGI PMID:14752163 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:14752163 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:21841778 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002497 increased IgE level IAGP N RGD:5509061 20200310 MGI PMID:14752163 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002497 increased IgE level IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002869 increased anti-insulin autoantibody level IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0004969 pale kidney IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200310 MGI PMID:14752163 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0005015 increased T cell number IAGP N RGD:5509061 20200310 MGI PMID:21841778 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21841778 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21841778 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:21841778 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:21841778 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20200310 MGI PMID:21841778 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20200310 MGI PMID:14752163 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008191 abnormal follicular B cell physiology IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20200310 MGI PMID:19299707 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20200310 MGI PMID:14752163 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20200310 MGI PMID:21841778 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20200310 MGI PMID:21841778 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:14752163 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:14752163 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:21841778 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20200310 MGI PMID:21841778 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20200310 MGI PMID:21841778 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0009922 increased transitional stage T1 B cell number IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552858 Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:23619366 1552859 Slc1a4 solute carrier family 1 (glutamate/neutral amino acid transporter), member 4 gene MP:0000433 microcephaly IAGP N RGD:5509061 20240201 MGI PMID:37642681 1552859 Slc1a4 solute carrier family 1 (glutamate/neutral amino acid transporter), member 4 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20240201 MGI PMID:37642681 1552859 Slc1a4 solute carrier family 1 (glutamate/neutral amino acid transporter), member 4 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20240201 MGI PMID:37642681 1552859 Slc1a4 solute carrier family 1 (glutamate/neutral amino acid transporter), member 4 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20240201 MGI PMID:37642681 1552859 Slc1a4 solute carrier family 1 (glutamate/neutral amino acid transporter), member 4 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20240201 MGI PMID:37642681 1552859 Slc1a4 solute carrier family 1 (glutamate/neutral amino acid transporter), member 4 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 1552859 Slc1a4 solute carrier family 1 (glutamate/neutral amino acid transporter), member 4 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1552859 Slc1a4 solute carrier family 1 (glutamate/neutral amino acid transporter), member 4 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1552861 Ascc3 activating signal cointegrator 1 complex subunit 3 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20200310 MGI 1552861 Ascc3 activating signal cointegrator 1 complex subunit 3 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20200310 MGI 1552861 Ascc3 activating signal cointegrator 1 complex subunit 3 gene MP:0004357 long tibia IEA N RGD:5509061 20200310 MGI 1552861 Ascc3 activating signal cointegrator 1 complex subunit 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1552862 Phc3 polyhomeotic 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1552862 Phc3 polyhomeotic 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1552862 Phc3 polyhomeotic 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1552862 Phc3 polyhomeotic 3 gene MP:0004956 decreased thymus weight IEA N RGD:5509061 20220519 MGI 1552864 Eif3h eukaryotic translation initiation factor 3, subunit H gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1552864 Eif3h eukaryotic translation initiation factor 3, subunit H gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20141003 MGI PMID:23173090 1552864 Eif3h eukaryotic translation initiation factor 3, subunit H gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23173090 1552864 Eif3h eukaryotic translation initiation factor 3, subunit H gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1552864 Eif3h eukaryotic translation initiation factor 3, subunit H gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23173090 1552864 Eif3h eukaryotic translation initiation factor 3, subunit H gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20141003 MGI PMID:23173090 1552865 Entpd3 ectonucleoside triphosphate diphosphohydrolase 3 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20190815 MGI PMID:25717362 1552865 Entpd3 ectonucleoside triphosphate diphosphohydrolase 3 gene MP:0010073 decreased pruritus IAGP N RGD:5509061 20190815 MGI PMID:25717362 1552866 Oit3 oncoprotein induced transcript 3 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:22306318 1552866 Oit3 oncoprotein induced transcript 3 gene MP:0008822 decreased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:22306318 1552866 Oit3 oncoprotein induced transcript 3 gene MP:0011424 decreased urine uric acid level IAGP N RGD:5509061 20141003 MGI PMID:22306318 1552867 Per1 period circadian clock 1 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:18367514 1552867 Per1 period circadian clock 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18367514 1552867 Per1 period circadian clock 1 gene MP:0001432 abnormal food preference IAGP N RGD:5509061 20141003 MGI PMID:18367514 1552867 Per1 period circadian clock 1 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:15031135 1552867 Per1 period circadian clock 1 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:18367514 1552867 Per1 period circadian clock 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:23267082 1552867 Per1 period circadian clock 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:18367514 1552867 Per1 period circadian clock 1 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:18367514 1552867 Per1 period circadian clock 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18367514 1552867 Per1 period circadian clock 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20150521 MGI PMID:25673850 1552867 Per1 period circadian clock 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:16143109 1552867 Per1 period circadian clock 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16143109 1552867 Per1 period circadian clock 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20150521 MGI PMID:25673850 1552867 Per1 period circadian clock 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:16143109 1552867 Per1 period circadian clock 1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:15031135 1552867 Per1 period circadian clock 1 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:18367514 1552867 Per1 period circadian clock 1 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:16143109 1552867 Per1 period circadian clock 1 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20150521 MGI PMID:25673850 1552867 Per1 period circadian clock 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16143109 1552867 Per1 period circadian clock 1 gene MP:0008961 abnormal basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:18367514 1552867 Per1 period circadian clock 1 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:18367514 1552867 Per1 period circadian clock 1 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:18367514 1552867 Per1 period circadian clock 1 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:18367514 1552867 Per1 period circadian clock 1 gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20150521 MGI PMID:25673850 1552867 Per1 period circadian clock 1 gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15031135 1552867 Per1 period circadian clock 1 gene MP:0011478 abnormal urine catecholamine level IAGP N RGD:5509061 20141003 MGI PMID:16143109 1552867 Per1 period circadian clock 1 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20171012 MGI PMID:23267082 1552867 Per1 period circadian clock 1 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:15031135 1552867 Per1 period circadian clock 1 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:11483500 1552867 Per1 period circadian clock 1 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:11389837 1552867 Per1 period circadian clock 1 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:11395012 1552867 Per1 period circadian clock 1 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:15031135 1552867 Per1 period circadian clock 1 gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:15888647 1552867 Per1 period circadian clock 1 gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:15888647 1552867 Per1 period circadian clock 1 gene MP:0020478 abnormal circadian sleep/wake cycle IAGP N RGD:5509061 20171012 MGI PMID:15031135 1552867 Per1 period circadian clock 1 gene MP:0030438 increased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:16143109 1552867 Per1 period circadian clock 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:25673850 1552868 Marchf1 membrane associated ring-CH-type finger 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:23712430 1552868 Marchf1 membrane associated ring-CH-type finger 1 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20200310 MGI PMID:19917682 1552868 Marchf1 membrane associated ring-CH-type finger 1 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20200310 MGI PMID:23712430 1552868 Marchf1 membrane associated ring-CH-type finger 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20200310 MGI PMID:17255932 1552868 Marchf1 membrane associated ring-CH-type finger 1 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20200310 MGI PMID:23712430 1552868 Marchf1 membrane associated ring-CH-type finger 1 gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20200310 MGI PMID:17255932 1552868 Marchf1 membrane associated ring-CH-type finger 1 gene MP:0005461 abnormal dendritic cell morphology IAGP N RGD:5509061 20200310 MGI PMID:17255932 1552868 Marchf1 membrane associated ring-CH-type finger 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:27503071 1552868 Marchf1 membrane associated ring-CH-type finger 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20200310 MGI PMID:19917682 1552868 Marchf1 membrane associated ring-CH-type finger 1 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20200310 MGI PMID:19917682 1552869 Ankrd35 ankyrin repeat domain 35 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201231 MGI 1552870 Pnlip pancreatic lipase gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:12915407 1552870 Pnlip pancreatic lipase gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:17604277 1552870 Pnlip pancreatic lipase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17604277 1552870 Pnlip pancreatic lipase gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17604277 1552870 Pnlip pancreatic lipase gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17604277 1552870 Pnlip pancreatic lipase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17604277 1552870 Pnlip pancreatic lipase gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17604277 1552870 Pnlip pancreatic lipase gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:12915407 1552870 Pnlip pancreatic lipase gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:17604277 1552870 Pnlip pancreatic lipase gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12915407 1552870 Pnlip pancreatic lipase gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17604277 1552870 Pnlip pancreatic lipase gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17604277 1552870 Pnlip pancreatic lipase gene MP:0014480 increased feces cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:12915407 1552871 Adamts5 ADAM metallopeptidase with thrombospondin type 1 motif 5 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15800625 1552871 Adamts5 ADAM metallopeptidase with thrombospondin type 1 motif 5 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:19922873 1552871 Adamts5 ADAM metallopeptidase with thrombospondin type 1 motif 5 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141120 MGI PMID:24753090 1552871 Adamts5 ADAM metallopeptidase with thrombospondin type 1 motif 5 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:19922873 1552871 Adamts5 ADAM metallopeptidase with thrombospondin type 1 motif 5 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:20036347 1552871 Adamts5 ADAM metallopeptidase with thrombospondin type 1 motif 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15800624 1552871 Adamts5 ADAM metallopeptidase with thrombospondin type 1 motif 5 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:15800624 1552871 Adamts5 ADAM metallopeptidase with thrombospondin type 1 motif 5 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20036347 1552871 Adamts5 ADAM metallopeptidase with thrombospondin type 1 motif 5 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:15800625 1552871 Adamts5 ADAM metallopeptidase with thrombospondin type 1 motif 5 gene MP:0009874 abnormal interdigital cell death IAGP N RGD:5509061 20141003 MGI PMID:19922873 1552874 Fut7 fucosyltransferase 7 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11485743 1552874 Fut7 fucosyltransferase 7 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11485743 1552874 Fut7 fucosyltransferase 7 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10982764 1552874 Fut7 fucosyltransferase 7 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16452210 1552874 Fut7 fucosyltransferase 7 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:8752218 1552874 Fut7 fucosyltransferase 7 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11485743 1552874 Fut7 fucosyltransferase 7 gene MP:0002345 abnormal lymph node primary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11485743 1552874 Fut7 fucosyltransferase 7 gene MP:0002345 abnormal lymph node primary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:8752218 1552874 Fut7 fucosyltransferase 7 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12869507 1552874 Fut7 fucosyltransferase 7 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11485743 1552874 Fut7 fucosyltransferase 7 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:8752218 1552874 Fut7 fucosyltransferase 7 gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:8752218 1552874 Fut7 fucosyltransferase 7 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:11485743 1552874 Fut7 fucosyltransferase 7 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:11485743 1552874 Fut7 fucosyltransferase 7 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:11485743 1552874 Fut7 fucosyltransferase 7 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:8752218 1552874 Fut7 fucosyltransferase 7 gene MP:0003627 abnormal leukocyte tethering or rolling IAGP N RGD:5509061 20141003 MGI PMID:8752218 1552874 Fut7 fucosyltransferase 7 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:8752218 1552874 Fut7 fucosyltransferase 7 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15308551 1552874 Fut7 fucosyltransferase 7 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11535629 1552874 Fut7 fucosyltransferase 7 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11859099 1552874 Fut7 fucosyltransferase 7 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11485743 1552874 Fut7 fucosyltransferase 7 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11535629 1552874 Fut7 fucosyltransferase 7 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8752218 1552874 Fut7 fucosyltransferase 7 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:11485743 1552874 Fut7 fucosyltransferase 7 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:8752218 1552874 Fut7 fucosyltransferase 7 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10982764 1552874 Fut7 fucosyltransferase 7 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:11485743 1552877 Or1e32 olfactory receptor family 1 subfamily E member 32 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20230601 MGI 1552877 Or1e32 olfactory receptor family 1 subfamily E member 32 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20230601 MGI 1552877 Or1e32 olfactory receptor family 1 subfamily E member 32 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1552877 Or1e32 olfactory receptor family 1 subfamily E member 32 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1552877 Or1e32 olfactory receptor family 1 subfamily E member 32 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1552877 Or1e32 olfactory receptor family 1 subfamily E member 32 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1552877 Or1e32 olfactory receptor family 1 subfamily E member 32 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1552877 Or1e32 olfactory receptor family 1 subfamily E member 32 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 1552877 Or1e32 olfactory receptor family 1 subfamily E member 32 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20230601 MGI 1552878 Prok2 prokineticin 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:15976302 1552878 Prok2 prokineticin 2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:15976302 1552878 Prok2 prokineticin 2 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:15976302 1552880 Mtch2 mitochondrial carrier 2 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20181227 MGI 1552880 Mtch2 mitochondrial carrier 2 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 1552880 Mtch2 mitochondrial carrier 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20151217 MGI PMID:20436477 1552880 Mtch2 mitochondrial carrier 2 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20151217 MGI PMID:20436477 1552880 Mtch2 mitochondrial carrier 2 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20151217 MGI PMID:20436477 1552880 Mtch2 mitochondrial carrier 2 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20151217 MGI PMID:20436477 1552880 Mtch2 mitochondrial carrier 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20436477 1552880 Mtch2 mitochondrial carrier 2 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20151217 MGI PMID:20436477 1552880 Mtch2 mitochondrial carrier 2 gene MP:0003326 liver failure IAGP N RGD:5509061 20141003 MGI PMID:20436477 1552880 Mtch2 mitochondrial carrier 2 gene MP:0005030 absent amnion IAGP N RGD:5509061 20151217 MGI PMID:20436477 1552880 Mtch2 mitochondrial carrier 2 gene MP:0009593 absent chorion IAGP N RGD:5509061 20151217 MGI PMID:20436477 1552880 Mtch2 mitochondrial carrier 2 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20436477 1552880 Mtch2 mitochondrial carrier 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552880 Mtch2 mitochondrial carrier 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21565393 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:21593405 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:21593405 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20160811 MGI PMID:20923861 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:21593405 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:21593405 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20160811 MGI PMID:20923861 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:21565393 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20160811 MGI PMID:20923861 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:21593405 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21593405 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:21593405 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:21565393 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21565393 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0005036 diarrhea IAGP N RGD:5509061 20180111 MGI PMID:28636595 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20160811 MGI PMID:20923861 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0008136 enlarged Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:21565393 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:21565393 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:21593405 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:21565393 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:21565393 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21593405 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0008896 increased IgG2c level IAGP N RGD:5509061 20141003 MGI PMID:21565393 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21565393 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21593405 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:21593405 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:21593405 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21593405 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20141003 MGI PMID:21565393 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0011431 increased urine flow rate IAGP N RGD:5509061 20160811 MGI PMID:20923861 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20160811 MGI PMID:20923861 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20160811 MGI PMID:20923861 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:21593405 1552887 Nlrp6 NLR family, pyrin domain containing 6 gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:28636595 1552891 Stk40 serine/threonine kinase 40 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20200310 MGI PMID:23293024 1552891 Stk40 serine/threonine kinase 40 gene MP:0001177 atelectasis IAGP N RGD:5509061 20200310 MGI PMID:23293024 1552891 Stk40 serine/threonine kinase 40 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:23293024 1552891 Stk40 serine/threonine kinase 40 gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:23293024 1552891 Stk40 serine/threonine kinase 40 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:23293024 1552891 Stk40 serine/threonine kinase 40 gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20200310 MGI PMID:23293024 1552891 Stk40 serine/threonine kinase 40 gene MP:0003641 small lung IAGP N RGD:5509061 20200310 MGI PMID:23293024 1552891 Stk40 serine/threonine kinase 40 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20200310 MGI PMID:23293024 1552891 Stk40 serine/threonine kinase 40 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20200310 MGI PMID:23293024 1552891 Stk40 serine/threonine kinase 40 gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20200310 MGI PMID:23293024 1552891 Stk40 serine/threonine kinase 40 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23293024 1552891 Stk40 serine/threonine kinase 40 gene MP:0030002 increased lung apoptosis IAGP N RGD:5509061 20200310 MGI PMID:23293024 1552891 Stk40 serine/threonine kinase 40 gene MP:0031006 increased lung glycogen level IAGP N RGD:5509061 20200310 MGI PMID:23293024 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20221201 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20221201 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20221201 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20221201 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0001860 liver inflammation IAGP N RGD:5509061 20221201 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20221201 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20221201 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0002981 increased liver weight IAGP N RGD:5509061 20221201 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20221201 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20221201 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20221201 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20221201 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20221201 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0008990 abnormal Ito cell morphology IAGP N RGD:5509061 20221201 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20240530 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20221201 MGI PMID:26458163 1552892 Ssu72 Ssu72 RNA polymerase II CTD phosphatase homolog (yeast) gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1552893 Lefty2 left-right determination factor 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0000542 left-sided isomerism IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:10518210 1552893 Lefty2 left-right determination factor 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:10518210 1552893 Lefty2 left-right determination factor 2 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:10518210 1552893 Lefty2 left-right determination factor 2 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:10518210 1552893 Lefty2 left-right determination factor 2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:10518210 1552893 Lefty2 left-right determination factor 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:10518210 1552893 Lefty2 left-right determination factor 2 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:10518210 1552893 Lefty2 left-right determination factor 2 gene MP:0003284 abnormal large intestine placement IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0003342 accessory spleen IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0003872 absent heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0006063 abnormal inferior vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0006123 tricuspid valve atresia IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:10518210 1552893 Lefty2 left-right determination factor 2 gene MP:0008461 left atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:10518210 1552893 Lefty2 left-right determination factor 2 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:10518210 1552893 Lefty2 left-right determination factor 2 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0010426 abnormal heart and great artery attachment IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0010668 abnormal hepatic portal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11703930 1552893 Lefty2 left-right determination factor 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10518210 1552893 Lefty2 left-right determination factor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10518210 1552893 Lefty2 left-right determination factor 2 gene MP:0011257 abnormal head fold morphology IAGP N RGD:5509061 20141003 MGI PMID:10518210 1552893 Lefty2 left-right determination factor 2 gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:10518210 1552894 Ggps1 geranylgeranyl diphosphate synthase 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1552894 Ggps1 geranylgeranyl diphosphate synthase 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20160421 MGI 1552894 Ggps1 geranylgeranyl diphosphate synthase 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1552894 Ggps1 geranylgeranyl diphosphate synthase 1 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1552894 Ggps1 geranylgeranyl diphosphate synthase 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20201022 MGI 1552894 Ggps1 geranylgeranyl diphosphate synthase 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1552894 Ggps1 geranylgeranyl diphosphate synthase 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1552894 Ggps1 geranylgeranyl diphosphate synthase 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20160421 MGI 1552894 Ggps1 geranylgeranyl diphosphate synthase 1 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20220811 MGI 1552894 Ggps1 geranylgeranyl diphosphate synthase 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1552894 Ggps1 geranylgeranyl diphosphate synthase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552895 Cd1d1 CD1d1 antigen gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:15485631 1552895 Cd1d1 CD1d1 antigen gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:16675847 1552895 Cd1d1 CD1d1 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15958069 1552895 Cd1d1 CD1d1 antigen gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11550008 1552895 Cd1d1 CD1d1 antigen gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:21921158 1552895 Cd1d1 CD1d1 antigen gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:11731798 1552895 Cd1d1 CD1d1 antigen gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:16339525 1552895 Cd1d1 CD1d1 antigen gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:12902521 1552895 Cd1d1 CD1d1 antigen gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:21921158 1552895 Cd1d1 CD1d1 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20171214 MGI PMID:21964024 1552895 Cd1d1 CD1d1 antigen gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21921158 1552895 Cd1d1 CD1d1 antigen gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:19587020 1552895 Cd1d1 CD1d1 antigen gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20230601 MGI 1552895 Cd1d1 CD1d1 antigen gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:12902521 1552895 Cd1d1 CD1d1 antigen gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:12902521 1552895 Cd1d1 CD1d1 antigen gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:21921158 1552895 Cd1d1 CD1d1 antigen gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12902521 1552895 Cd1d1 CD1d1 antigen gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:15958069 1552895 Cd1d1 CD1d1 antigen gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:12902521 1552895 Cd1d1 CD1d1 antigen gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:12902521 1552895 Cd1d1 CD1d1 antigen gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16675847 1552895 Cd1d1 CD1d1 antigen gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16339525 1552895 Cd1d1 CD1d1 antigen gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:15485631 1552895 Cd1d1 CD1d1 antigen gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15591216 1552895 Cd1d1 CD1d1 antigen gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12902521 1552895 Cd1d1 CD1d1 antigen gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15591216 1552895 Cd1d1 CD1d1 antigen gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15591216 1552895 Cd1d1 CD1d1 antigen gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:12902521 1552895 Cd1d1 CD1d1 antigen gene MP:0008036 abnormal NK T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19587020 1552895 Cd1d1 CD1d1 antigen gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:10201995 1552895 Cd1d1 CD1d1 antigen gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:11731798 1552895 Cd1d1 CD1d1 antigen gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:19587020 1552895 Cd1d1 CD1d1 antigen gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:22393151 1552895 Cd1d1 CD1d1 antigen gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:9133426 1552895 Cd1d1 CD1d1 antigen gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19587020 1552895 Cd1d1 CD1d1 antigen gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:16675847 1552895 Cd1d1 CD1d1 antigen gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21921158 1552895 Cd1d1 CD1d1 antigen gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:12902521 1552895 Cd1d1 CD1d1 antigen gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15485631 1552895 Cd1d1 CD1d1 antigen gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15485631 1552895 Cd1d1 CD1d1 antigen gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22393151 1552895 Cd1d1 CD1d1 antigen gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9133426 1552895 Cd1d1 CD1d1 antigen gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19587020 1552895 Cd1d1 CD1d1 antigen gene MP:0008698 abnormal interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19587020 1552895 Cd1d1 CD1d1 antigen gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:12902521 1552895 Cd1d1 CD1d1 antigen gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:22393151 1552895 Cd1d1 CD1d1 antigen gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:9133426 1552895 Cd1d1 CD1d1 antigen gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20230601 MGI 1552895 Cd1d1 CD1d1 antigen gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15485631 1552895 Cd1d1 CD1d1 antigen gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21921158 1552895 Cd1d1 CD1d1 antigen gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20230601 MGI 1552895 Cd1d1 CD1d1 antigen gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:12902521 1552895 Cd1d1 CD1d1 antigen gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:12902521 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:20392939 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17250763 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9736643 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0000771 abnormal brain size IAGP N RGD:5509061 20141003 MGI PMID:8995755 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17250763 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:8995755 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:14686897 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:17250763 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8995755 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001349 excessive tearing IAGP N RGD:5509061 20141003 MGI PMID:8995755 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:17250763 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9736643 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:8995755 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17250763 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:9581771 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:17250763 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:8995755 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:12612586 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:9736643 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:9736643 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:20392939 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001849 ear inflammation IAGP N RGD:5509061 20141003 MGI PMID:17250763 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:17250763 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:8995755 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:17250763 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:9718989 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0001994 increased blinking frequency IAGP N RGD:5509061 20141003 MGI PMID:9581771 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:14686897 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:20392939 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:9581771 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:9736643 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141127 MGI PMID:24270080 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20392939 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9581771 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17250763 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:8995755 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:8995755 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8995755 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:9581771 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12611922 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:8995755 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:9581771 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:9736643 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002918 abnormal paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:9581771 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12612586 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:20392939 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0003483 decreased nerve fiber response threshold IAGP N RGD:5509061 20141003 MGI PMID:12611922 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141127 MGI PMID:24270080 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:14686897 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20392939 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:9581771 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:9718989 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:9581771 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:9581771 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:14686896 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:8995755 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:20392939 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:12611922 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:9581771 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0005654 porphyria IAGP N RGD:5509061 20141003 MGI PMID:17250763 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0008282 enlarged hippocampus IAGP N RGD:5509061 20141003 MGI PMID:17250763 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0008532 decreased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:9718989 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20141003 MGI PMID:20392939 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:20392939 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141127 MGI PMID:24270080 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20392939 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12612586 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0013468 chromodacryorrhea IAGP N RGD:5509061 20150205 MGI PMID:8995755 1552897 Kcna1 potassium voltage-gated channel, shaker-related subfamily, member 1 gene MP:0014253 decreased paired-pulse ratio IAGP N RGD:5509061 20230706 MGI PMID:24270080 1552898 Crybb2 crystallin, beta B2 gene MP:0000879 increased Purkinje cell number IAGP N RGD:5509061 20200310 MGI PMID:18385073 1552898 Crybb2 crystallin, beta B2 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220428 MGI PMID:25245288 1552898 Crybb2 crystallin, beta B2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:18719080 1552898 Crybb2 crystallin, beta B2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20200310 MGI PMID:11381063 1552898 Crybb2 crystallin, beta B2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20200310 MGI PMID:18385073 1552898 Crybb2 crystallin, beta B2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20200310 MGI PMID:7363969 1552898 Crybb2 crystallin, beta B2 gene MP:0001304 cataract IAGP N RGD:5509061 20200310 MGI PMID:11381063 1552898 Crybb2 crystallin, beta B2 gene MP:0001304 cataract IAGP N RGD:5509061 20200310 MGI PMID:18385073 1552898 Crybb2 crystallin, beta B2 gene MP:0001304 cataract IAGP N RGD:5509061 20200310 MGI PMID:18719080 1552898 Crybb2 crystallin, beta B2 gene MP:0001306 small lens IAGP N RGD:5509061 20200310 MGI PMID:18385073 1552898 Crybb2 crystallin, beta B2 gene MP:0001306 small lens IAGP N RGD:5509061 20200310 MGI PMID:18719080 1552898 Crybb2 crystallin, beta B2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220428 MGI PMID:25245288 1552898 Crybb2 crystallin, beta B2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220428 MGI PMID:25245288 1552898 Crybb2 crystallin, beta B2 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20220428 MGI PMID:25245288 1552898 Crybb2 crystallin, beta B2 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:11381063 1552898 Crybb2 crystallin, beta B2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20220428 MGI PMID:25245288 1552898 Crybb2 crystallin, beta B2 gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20220428 MGI PMID:25245288 1552898 Crybb2 crystallin, beta B2 gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20220428 MGI PMID:25245288 1552898 Crybb2 crystallin, beta B2 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20220428 MGI PMID:25245288 1552898 Crybb2 crystallin, beta B2 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20200310 MGI PMID:18719080 1552898 Crybb2 crystallin, beta B2 gene MP:0010251 subcapsular cataract IAGP N RGD:5509061 20200310 MGI PMID:7363969 1552898 Crybb2 crystallin, beta B2 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20200310 MGI PMID:7363969 1552898 Crybb2 crystallin, beta B2 gene MP:0010256 anterior cortical cataract IAGP N RGD:5509061 20220428 MGI PMID:18719080 1552898 Crybb2 crystallin, beta B2 gene MP:0010257 posterior cortical cataract IAGP N RGD:5509061 20220428 MGI PMID:18719080 1552898 Crybb2 crystallin, beta B2 gene MP:0010261 sutural cataract IEA N RGD:5509061 20200310 MGI 1552898 Crybb2 crystallin, beta B2 gene MP:0010263 total cataract IAGP N RGD:5509061 20200310 MGI PMID:11381063 1552898 Crybb2 crystallin, beta B2 gene MP:0010263 total cataract IAGP N RGD:5509061 20220428 MGI PMID:18719080 1552898 Crybb2 crystallin, beta B2 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220428 MGI PMID:25245288 1552898 Crybb2 crystallin, beta B2 gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20220428 MGI PMID:25245288 1552898 Crybb2 crystallin, beta B2 gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:18385073 1552898 Crybb2 crystallin, beta B2 gene MP:0031018 decreased granulosa cell proliferation IAGP N RGD:5509061 20220428 MGI PMID:25245288 1552898 Crybb2 crystallin, beta B2 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220428 MGI PMID:25245288 1552898 Crybb2 crystallin, beta B2 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220428 MGI PMID:25245288 1552898 Crybb2 crystallin, beta B2 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:25245288 1552899 Cd180 CD180 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:18492657 1552899 Cd180 CD180 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:18492657 1552899 Cd180 CD180 antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20200310 MGI PMID:10880523 1552899 Cd180 CD180 antigen gene MP:0001863 blood vessel inflammation IAGP N RGD:5509061 20200310 MGI PMID:18492657 1552899 Cd180 CD180 antigen gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20200310 MGI PMID:18492657 1552899 Cd180 CD180 antigen gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20200310 MGI PMID:18492657 1552899 Cd180 CD180 antigen gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200310 MGI PMID:18492657 1552899 Cd180 CD180 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:18492657 1552899 Cd180 CD180 antigen gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20200310 MGI PMID:18492657 1552899 Cd180 CD180 antigen gene MP:0005265 abnormal blood urea nitrogen level IAGP N RGD:5509061 20200310 MGI PMID:18492657 1552899 Cd180 CD180 antigen gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18492657 1552899 Cd180 CD180 antigen gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:18492657 1552899 Cd180 CD180 antigen gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20200310 MGI PMID:18492657 1552899 Cd180 CD180 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20200310 MGI PMID:18492657 1552901 Tmem63b transmembrane protein 63b gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20200310 MGI 1552901 Tmem63b transmembrane protein 63b gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1552901 Tmem63b transmembrane protein 63b gene MP:0001513 limb grasping IEA N RGD:5509061 20200310 MGI 1552901 Tmem63b transmembrane protein 63b gene MP:0001967 deafness IAGP N RGD:5509061 20210429 MGI PMID:32375046 1552901 Tmem63b transmembrane protein 63b gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1552901 Tmem63b transmembrane protein 63b gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20210429 MGI PMID:32375046 1552901 Tmem63b transmembrane protein 63b gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20210429 MGI PMID:32375046 1552901 Tmem63b transmembrane protein 63b gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20210429 MGI PMID:32375046 1552901 Tmem63b transmembrane protein 63b gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1552901 Tmem63b transmembrane protein 63b gene MP:0006325 impaired hearing IAGP N RGD:5509061 20210429 MGI PMID:32375046 1552901 Tmem63b transmembrane protein 63b gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552901 Tmem63b transmembrane protein 63b gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20210429 MGI PMID:32375046 1552903 Or9g4 olfactory receptor family 9 subfamily G member 4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1552903 Or9g4 olfactory receptor family 9 subfamily G member 4 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 1552903 Or9g4 olfactory receptor family 9 subfamily G member 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1552903 Or9g4 olfactory receptor family 9 subfamily G member 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1552903 Or9g4 olfactory receptor family 9 subfamily G member 4 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1552903 Or9g4 olfactory receptor family 9 subfamily G member 4 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1552903 Or9g4 olfactory receptor family 9 subfamily G member 4 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230601 MGI 1552903 Or9g4 olfactory receptor family 9 subfamily G member 4 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1552903 Or9g4 olfactory receptor family 9 subfamily G member 4 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20230601 MGI 1552903 Or9g4 olfactory receptor family 9 subfamily G member 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1552903 Or9g4 olfactory receptor family 9 subfamily G member 4 gene MP:0002188 small heart IEA N RGD:5509061 20230601 MGI 1552903 Or9g4 olfactory receptor family 9 subfamily G member 4 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1552903 Or9g4 olfactory receptor family 9 subfamily G member 4 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20231207 MGI 1552903 Or9g4 olfactory receptor family 9 subfamily G member 4 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 1552903 Or9g4 olfactory receptor family 9 subfamily G member 4 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20231207 MGI 1552904 Rab21 RAB21, member RAS oncogene family gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1552904 Rab21 RAB21, member RAS oncogene family gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1552904 Rab21 RAB21, member RAS oncogene family gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1552904 Rab21 RAB21, member RAS oncogene family gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1552904 Rab21 RAB21, member RAS oncogene family gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552905 Lcmt1 leucine carboxyl methyltransferase 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1552905 Lcmt1 leucine carboxyl methyltransferase 1 gene MP:0000520 absent kidney IEA N RGD:5509061 20111116 MGI 1552905 Lcmt1 leucine carboxyl methyltransferase 1 gene MP:0001565 abnormal circulating phosphate level IEA N RGD:5509061 20230601 MGI 1552905 Lcmt1 leucine carboxyl methyltransferase 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23840384 1552905 Lcmt1 leucine carboxyl methyltransferase 1 gene MP:0003313 abnormal locomotor activation IEA N RGD:5509061 20220811 MGI 1552905 Lcmt1 leucine carboxyl methyltransferase 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1552905 Lcmt1 leucine carboxyl methyltransferase 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23840384 1552905 Lcmt1 leucine carboxyl methyltransferase 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23840384 1552905 Lcmt1 leucine carboxyl methyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17724024 1552905 Lcmt1 leucine carboxyl methyltransferase 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23840384 1552905 Lcmt1 leucine carboxyl methyltransferase 1 gene MP:0012360 abnormal large unstained cell number IEA N RGD:5509061 20211021 MGI 1552909 Zbtb44 zinc finger and BTB domain containing 44 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20141003 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:22560297 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:22560297 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:22560297 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11468159 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000239 absent common myeloid progenitor cells IAGP N RGD:5509061 20141003 MGI PMID:11468159 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12591246 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:12591246 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:17244677 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000640 adrenal gland hypoplasia IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:22560297 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:11468159 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:22560297 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22560297 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11912494 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11468159 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:17082260 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:11912494 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11468159 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11468159 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:17082260 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001705 abnormal proximal-distal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:11912494 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:11468159 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:17082260 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:17082260 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:17082260 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17244677 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002345 abnormal lymph node primary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17244677 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11468159 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:17082260 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11912494 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:12591246 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:12591246 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:11912494 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0003276 esophageal atresia IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12591246 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0003600 ectopic kidney IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0003600 ectopic kidney IAGP N RGD:5509061 20141003 MGI PMID:12591246 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:12591246 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17082260 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17082260 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:22315423 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0004344 scapular bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22560297 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20141003 MGI PMID:22560297 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:12591246 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20141003 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:22560297 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12591246 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:11912494 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0005224 abnormal left-right axis symmetry of the somites IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11912494 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:22560297 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20141003 MGI PMID:14595835 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0005492 exocrine pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11912494 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0005651 abnormal gonad rudiment morphology IAGP N RGD:5509061 20141003 MGI PMID:14595835 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0006338 abnormal second pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17244677 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17244677 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17244677 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18462698 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0009173 absent pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:11912494 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:11912494 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0010146 umbilical hernia IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0010788 stomach hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0010788 stomach hypoplasia IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0010807 abnormal stomach position or orientation IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0010982 abnormal ureteric bud elongation IAGP N RGD:5509061 20141003 MGI PMID:12591246 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:12591246 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0010987 abnormal nephrogenic mesenchyme morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12591246 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11468159 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17244677 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0011263 abnormal spleen mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:22560297 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:12591246 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:12591246 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0011361 pelvic kidney IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0011364 abnormal metanephros morphology IAGP N RGD:5509061 20141003 MGI PMID:12591246 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0012491 larynx stenosis IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0013497 trachea occlusion IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0013848 subcutaneous edema IAGP N RGD:5509061 20220512 MGI PMID:31625560 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0014107 premature chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0014287 decreased adrenal gland zona fasciculata size IAGP N RGD:5509061 20230907 MGI PMID:17082260 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0021210 bilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0021211 unilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0030190 small snout IAGP N RGD:5509061 20171019 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0030297 outer ear hypoplasia IAGP N RGD:5509061 20171221 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0030323 short styloid process IAGP N RGD:5509061 20171214 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0030465 absent oval window IAGP N RGD:5509061 20171221 MGI PMID:11566859 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0031447 unilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:21982646 1552910 Pbx1 pre B cell leukemia homeobox 1 gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:21982646 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230126 MGI PMID:33824276 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20230126 MGI PMID:33824276 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20230126 MGI PMID:33824276 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0003502 increased activity of thyroid gland IAGP N RGD:5509061 20230126 MGI PMID:33824276 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20230126 MGI PMID:33824276 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20230126 MGI PMID:33824276 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20230126 MGI PMID:33824276 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20230126 MGI PMID:33824276 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20230126 MGI PMID:33824276 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20230126 MGI PMID:33824276 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20230126 MGI PMID:33824276 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0011019 abnormal adaptive thermogenesis IAGP N RGD:5509061 20230126 MGI PMID:33824276 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552915 Adgra1 adhesion G protein-coupled receptor A1 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20230126 MGI PMID:33824276 1552917 C6 complement component 6 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:10811844 1552917 C6 complement component 6 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19959238 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15660130 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:15660130 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:15660130 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15660130 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15660130 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15660130 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15660130 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15660130 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15660130 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20240523 MGI 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15660130 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:15660130 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1552918 Dnaja1 DnaJ heat shock protein family (Hsp40) member A1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552921 Sgpp1 sphingosine-1-phosphate phosphatase 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23637227 1552921 Sgpp1 sphingosine-1-phosphate phosphatase 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:23637227 1552921 Sgpp1 sphingosine-1-phosphate phosphatase 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:23637227 1552921 Sgpp1 sphingosine-1-phosphate phosphatase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23637227 1552921 Sgpp1 sphingosine-1-phosphate phosphatase 1 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:23637227 1552921 Sgpp1 sphingosine-1-phosphate phosphatase 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:23637227 1552921 Sgpp1 sphingosine-1-phosphate phosphatase 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:23637227 1552921 Sgpp1 sphingosine-1-phosphate phosphatase 1 gene MP:0009474 thick epidermis stratum spinosum IAGP N RGD:5509061 20141003 MGI PMID:23637227 1552921 Sgpp1 sphingosine-1-phosphate phosphatase 1 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23637227 1552921 Sgpp1 sphingosine-1-phosphate phosphatase 1 gene MP:0009599 thick epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:23637227 1552921 Sgpp1 sphingosine-1-phosphate phosphatase 1 gene MP:0009715 thick epidermis stratum basale IAGP N RGD:5509061 20141003 MGI PMID:23637227 1552921 Sgpp1 sphingosine-1-phosphate phosphatase 1 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20170309 MGI PMID:23637227 1552921 Sgpp1 sphingosine-1-phosphate phosphatase 1 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20170309 MGI PMID:27059959 1552921 Sgpp1 sphingosine-1-phosphate phosphatase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23637227 1552921 Sgpp1 sphingosine-1-phosphate phosphatase 1 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20141003 MGI PMID:23637227 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20200310 MGI PMID:12629211 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20200310 MGI PMID:21333627 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:21333627 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200310 MGI PMID:12629211 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200310 MGI PMID:12629211 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200310 MGI PMID:12629211 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0004494 abnormal synaptic glutamate release IAGP N RGD:5509061 20200310 MGI PMID:16115873 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:12629211 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0009434 paraparesis IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0009765 abnormal xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:16115873 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0009978 abnormal cerebellum white matter morphology IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20200310 MGI PMID:21333627 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0010734 abnormal paranode morphology IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0010735 abnormal paranodal axoglial junction morphology IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0012231 abnormal ganglioside level IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0014114 abnormal cognition IAGP N RGD:5509061 20200310 MGI PMID:21333627 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20200310 MGI PMID:15710896 1552922 St3gal5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5 gene MP:0020194 abnormal glycosphingolipid level IAGP N RGD:5509061 20200310 MGI PMID:16115873 1552924 Tmco3 transmembrane and coiled-coil domains 3 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20220811 MGI 1552924 Tmco3 transmembrane and coiled-coil domains 3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210520 MGI 1552924 Tmco3 transmembrane and coiled-coil domains 3 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1552926 Tars3 threonyl-tRNA synthetase 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1552926 Tars3 threonyl-tRNA synthetase 3 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20231207 MGI 1552926 Tars3 threonyl-tRNA synthetase 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1552926 Tars3 threonyl-tRNA synthetase 3 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20231207 MGI 1552926 Tars3 threonyl-tRNA synthetase 3 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20231207 MGI 1552926 Tars3 threonyl-tRNA synthetase 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20231207 MGI 1552926 Tars3 threonyl-tRNA synthetase 3 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20240523 MGI 1552926 Tars3 threonyl-tRNA synthetase 3 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20240523 MGI 1552926 Tars3 threonyl-tRNA synthetase 3 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 1552926 Tars3 threonyl-tRNA synthetase 3 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20231207 MGI 1552926 Tars3 threonyl-tRNA synthetase 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20231207 MGI 1552930 Fgf14 fibroblast growth factor 14 gene MP:0000160 kyphosis IEA N RGD:5509061 20210520 MGI 1552930 Fgf14 fibroblast growth factor 14 gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20210826 MGI 1552930 Fgf14 fibroblast growth factor 14 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1552930 Fgf14 fibroblast growth factor 14 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:17678857 1552930 Fgf14 fibroblast growth factor 14 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20180201 MGI PMID:22855807 1552930 Fgf14 fibroblast growth factor 14 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20180201 MGI PMID:22855807 1552930 Fgf14 fibroblast growth factor 14 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12123606 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001263 weight loss IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20180201 MGI PMID:24503275 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20180201 MGI PMID:24503275 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20180201 MGI PMID:24503275 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12123606 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17678857 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001393 ataxia IAGP N RGD:5509061 20150716 MGI PMID:17236779 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17678857 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12123606 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150716 MGI PMID:17236779 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12123606 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17678857 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:17678857 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20180201 MGI PMID:24503275 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20180201 MGI PMID:16020737 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20150716 MGI PMID:17236779 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:12123606 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001505 hunched posture IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:12123606 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001513 limb grasping IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:12123606 1552930 Fgf14 fibroblast growth factor 14 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1552930 Fgf14 fibroblast growth factor 14 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12123606 1552930 Fgf14 fibroblast growth factor 14 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1552930 Fgf14 fibroblast growth factor 14 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20180201 MGI PMID:16020737 1552930 Fgf14 fibroblast growth factor 14 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17678857 1552930 Fgf14 fibroblast growth factor 14 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20150716 MGI PMID:18930825 1552930 Fgf14 fibroblast growth factor 14 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20180201 MGI PMID:16020737 1552930 Fgf14 fibroblast growth factor 14 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:12123606 1552930 Fgf14 fibroblast growth factor 14 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20221215 MGI 1552930 Fgf14 fibroblast growth factor 14 gene MP:0003214 neurofibrillary tangles IAGP N RGD:5509061 20180201 MGI PMID:16020737 1552930 Fgf14 fibroblast growth factor 14 gene MP:0003214 neurofibrillary tangles IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0003214 neurofibrillary tangles IAGP N RGD:5509061 20180201 MGI PMID:24503275 1552930 Fgf14 fibroblast growth factor 14 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:12123606 1552930 Fgf14 fibroblast growth factor 14 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:17678857 1552930 Fgf14 fibroblast growth factor 14 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12123606 1552930 Fgf14 fibroblast growth factor 14 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20210520 MGI 1552930 Fgf14 fibroblast growth factor 14 gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20180201 MGI PMID:24503275 1552930 Fgf14 fibroblast growth factor 14 gene MP:0005323 dystonia IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0005355 enlarged thyroid gland IEA N RGD:5509061 20210826 MGI 1552930 Fgf14 fibroblast growth factor 14 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20180201 MGI PMID:16020737 1552930 Fgf14 fibroblast growth factor 14 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20240627 MGI PMID:12123606 1552930 Fgf14 fibroblast growth factor 14 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20180201 MGI PMID:24503275 1552930 Fgf14 fibroblast growth factor 14 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20180201 MGI PMID:24503275 1552930 Fgf14 fibroblast growth factor 14 gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20180201 MGI PMID:16020737 1552930 Fgf14 fibroblast growth factor 14 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:12123606 1552930 Fgf14 fibroblast growth factor 14 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:17678857 1552930 Fgf14 fibroblast growth factor 14 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20150716 MGI PMID:17236779 1552930 Fgf14 fibroblast growth factor 14 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1552930 Fgf14 fibroblast growth factor 14 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20150716 MGI PMID:17236779 1552930 Fgf14 fibroblast growth factor 14 gene MP:0012508 forebrain atrophy IAGP N RGD:5509061 20180201 MGI PMID:16020737 1552930 Fgf14 fibroblast growth factor 14 gene MP:0012508 forebrain atrophy IAGP N RGD:5509061 20180201 MGI PMID:16291936 1552930 Fgf14 fibroblast growth factor 14 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:17236779 1552930 Fgf14 fibroblast growth factor 14 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:24503275 1552932 Npdc1 neural proliferation, differentiation and control 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15563841 1552934 Brix1 BRX1, biogenesis of ribosomes gene MP:0001488 increased startle reflex IEA N RGD:5509061 20231207 MGI 1552934 Brix1 BRX1, biogenesis of ribosomes gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20231207 MGI 1552934 Brix1 BRX1, biogenesis of ribosomes gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20231207 MGI 1552936 Pwwp3a PWWP domain containing 3A, DNA repair factor gene MP:0000706 small thymus IEA N RGD:5509061 20231207 MGI 1552936 Pwwp3a PWWP domain containing 3A, DNA repair factor gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1552936 Pwwp3a PWWP domain containing 3A, DNA repair factor gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1552936 Pwwp3a PWWP domain containing 3A, DNA repair factor gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1552936 Pwwp3a PWWP domain containing 3A, DNA repair factor gene MP:0005505 thrombocytosis IEA N RGD:5509061 20211021 MGI 1552936 Pwwp3a PWWP domain containing 3A, DNA repair factor gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20240523 MGI 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:14671308 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0002083 premature death IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:14671308 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:14671308 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:14671308 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552938 Mbnl1 muscleblind like splicing regulator 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20150305 MGI PMID:24293317 1552940 Tfap4 transcription factor AP4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1552940 Tfap4 transcription factor AP4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1552940 Tfap4 transcription factor AP4 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1552940 Tfap4 transcription factor AP4 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21873191 1552940 Tfap4 transcription factor AP4 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210826 MGI 1552940 Tfap4 transcription factor AP4 gene MP:0003049 abnormal lumbar vertebrae morphology IEA N RGD:5509061 20210826 MGI 1552940 Tfap4 transcription factor AP4 gene MP:0003050 abnormal sacral vertebrae morphology IEA N RGD:5509061 20210826 MGI 1552940 Tfap4 transcription factor AP4 gene MP:0003402 decreased liver weight IEA N RGD:5509061 20220519 MGI 1552940 Tfap4 transcription factor AP4 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1552940 Tfap4 transcription factor AP4 gene MP:0004956 decreased thymus weight IEA N RGD:5509061 20220519 MGI 1552940 Tfap4 transcription factor AP4 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1552940 Tfap4 transcription factor AP4 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1552940 Tfap4 transcription factor AP4 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1552940 Tfap4 transcription factor AP4 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1552940 Tfap4 transcription factor AP4 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1552940 Tfap4 transcription factor AP4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21873191 1552940 Tfap4 transcription factor AP4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1552941 Myrip myosin VIIA and Rab interacting protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191114 MGI PMID:28673385 1552941 Myrip myosin VIIA and Rab interacting protein gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20191114 MGI PMID:28673385 1552941 Myrip myosin VIIA and Rab interacting protein gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20191114 MGI PMID:28673385 1552941 Myrip myosin VIIA and Rab interacting protein gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20191114 MGI PMID:28673385 1552941 Myrip myosin VIIA and Rab interacting protein gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20191114 MGI PMID:28673385 1552942 Rhob ras homolog family member B gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:14597666 1552942 Rhob ras homolog family member B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14597666 1552942 Rhob ras homolog family member B gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:11564874 1552942 Rhob ras homolog family member B gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:14597666 1552942 Rhob ras homolog family member B gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:11564874 1552942 Rhob ras homolog family member B gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11564874 1552942 Rhob ras homolog family member B gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20180322 MGI PMID:19828736 1552942 Rhob ras homolog family member B gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11564874 1552942 Rhob ras homolog family member B gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:11564874 1552944 Kpna1 karyopherin subunit alpha 1 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:21371262 1552944 Kpna1 karyopherin subunit alpha 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21371262 1552944 Kpna1 karyopherin subunit alpha 1 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:21371262 1552944 Kpna1 karyopherin subunit alpha 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21371262 1552944 Kpna1 karyopherin subunit alpha 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21371262 1552944 Kpna1 karyopherin subunit alpha 1 gene MP:0003572 abnormal uterus development IAGP N RGD:5509061 20141003 MGI PMID:21371262 1552944 Kpna1 karyopherin subunit alpha 1 gene MP:0004514 dystocia IAGP N RGD:5509061 20141003 MGI PMID:21371262 1552944 Kpna1 karyopherin subunit alpha 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21371262 1552944 Kpna1 karyopherin subunit alpha 1 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:21371262 1552944 Kpna1 karyopherin subunit alpha 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21371262 1552944 Kpna1 karyopherin subunit alpha 1 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:21371262 1552944 Kpna1 karyopherin subunit alpha 1 gene MP:0008257 thin myometrium IAGP N RGD:5509061 20141003 MGI PMID:21371262 1552944 Kpna1 karyopherin subunit alpha 1 gene MP:0013400 abnormal endometrial gland development IAGP N RGD:5509061 20141218 MGI PMID:21371262 1552944 Kpna1 karyopherin subunit alpha 1 gene MP:0031137 vaginal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:21371262 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21333348 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0001565 abnormal circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21333348 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:21333348 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21333348 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:21333348 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:21333348 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0004955 increased thymus weight IEA N RGD:5509061 20211021 MGI 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210520 MGI 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0009199 abnormal external male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0009205 abnormal internal male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0011556 increased urine beta2-microglobulin level IAGP N RGD:5509061 20141003 MGI PMID:19050760 1552947 Gprc6a G protein-coupled receptor, family C, group 6, member A gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:21333348 1552948 Cetn1 centrin 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0030942 abnormal microtubule organizing center morphology IAGP N RGD:5509061 20191017 MGI PMID:23641067 1552948 Cetn1 centrin 1 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220303 MGI PMID:23641067 1552951 Impdh2 inosine monophosphate dehydrogenase 2 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12944494 1552951 Impdh2 inosine monophosphate dehydrogenase 2 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10953035 1552951 Impdh2 inosine monophosphate dehydrogenase 2 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12944494 1552951 Impdh2 inosine monophosphate dehydrogenase 2 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10953035 1552951 Impdh2 inosine monophosphate dehydrogenase 2 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12944494 1552951 Impdh2 inosine monophosphate dehydrogenase 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12944494 1552951 Impdh2 inosine monophosphate dehydrogenase 2 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12944494 1552951 Impdh2 inosine monophosphate dehydrogenase 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10953035 1552951 Impdh2 inosine monophosphate dehydrogenase 2 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10953035 1552955 Nrp1 neuropilin 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20200310 MGI PMID:11891274 1552955 Nrp1 neuropilin 1 gene MP:0000264 failure of vascular branching IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20200310 MGI PMID:10518505 1552955 Nrp1 neuropilin 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0000909 abnormal facial motor nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:15545635 1552955 Nrp1 neuropilin 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:15545635 1552955 Nrp1 neuropilin 1 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:15814794 1552955 Nrp1 neuropilin 1 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:15545635 1552955 Nrp1 neuropilin 1 gene MP:0001072 abnormal vestibulocochlear nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:15814794 1552955 Nrp1 neuropilin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:24401374 1552955 Nrp1 neuropilin 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:11891274 1552955 Nrp1 neuropilin 1 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20200310 MGI PMID:10518505 1552955 Nrp1 neuropilin 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:11891274 1552955 Nrp1 neuropilin 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:24401374 1552955 Nrp1 neuropilin 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20200310 MGI PMID:20512151 1552955 Nrp1 neuropilin 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:20512151 1552955 Nrp1 neuropilin 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20200310 MGI PMID:10518505 1552955 Nrp1 neuropilin 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20200310 MGI PMID:15550623 1552955 Nrp1 neuropilin 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20200310 MGI PMID:10518505 1552955 Nrp1 neuropilin 1 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20200310 MGI PMID:27844052 1552955 Nrp1 neuropilin 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:24401374 1552955 Nrp1 neuropilin 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20200310 MGI PMID:15814794 1552955 Nrp1 neuropilin 1 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:11891274 1552955 Nrp1 neuropilin 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:24401374 1552955 Nrp1 neuropilin 1 gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:24401374 1552955 Nrp1 neuropilin 1 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20200310 MGI PMID:11891274 1552955 Nrp1 neuropilin 1 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20200310 MGI PMID:24401374 1552955 Nrp1 neuropilin 1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20200310 MGI PMID:10518505 1552955 Nrp1 neuropilin 1 gene MP:0004159 double aortic arch IAGP N RGD:5509061 20200310 MGI PMID:10518505 1552955 Nrp1 neuropilin 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1552955 Nrp1 neuropilin 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20200310 MGI PMID:10518505 1552955 Nrp1 neuropilin 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20200310 MGI PMID:11891274 1552955 Nrp1 neuropilin 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:21828096 1552955 Nrp1 neuropilin 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:24401374 1552955 Nrp1 neuropilin 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20200310 MGI PMID:10518505 1552955 Nrp1 neuropilin 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20200310 MGI PMID:24401374 1552955 Nrp1 neuropilin 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20200310 MGI PMID:15545635 1552955 Nrp1 neuropilin 1 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20200310 MGI PMID:10518505 1552955 Nrp1 neuropilin 1 gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20200310 MGI PMID:10518505 1552955 Nrp1 neuropilin 1 gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20200310 MGI PMID:10518505 1552955 Nrp1 neuropilin 1 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20200310 MGI PMID:21828096 1552955 Nrp1 neuropilin 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1552955 Nrp1 neuropilin 1 gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20200310 MGI PMID:24401374 1552955 Nrp1 neuropilin 1 gene MP:0009945 abnormal accessory olfactory bulb morphology IAGP N RGD:5509061 20200310 MGI PMID:22745317 1552955 Nrp1 neuropilin 1 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:24401374 1552955 Nrp1 neuropilin 1 gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20200310 MGI PMID:21852397 1552955 Nrp1 neuropilin 1 gene MP:0010355 abnormal first pharyngeal arch artery morphology IAGP N RGD:5509061 20200310 MGI PMID:10518505 1552955 Nrp1 neuropilin 1 gene MP:0010356 abnormal second pharyngeal arch artery morphology IAGP N RGD:5509061 20200310 MGI PMID:10518505 1552955 Nrp1 neuropilin 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0010464 abnormal aortic arch and aortic arch branch attachment IAGP N RGD:5509061 20200310 MGI PMID:10518505 1552955 Nrp1 neuropilin 1 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:24401374 1552955 Nrp1 neuropilin 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24401374 1552955 Nrp1 neuropilin 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12852851 1552955 Nrp1 neuropilin 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10518505 1552955 Nrp1 neuropilin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11891274 1552955 Nrp1 neuropilin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552956 St8sia6 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1552956 St8sia6 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1552956 St8sia6 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6 gene MP:0001304 cataract IEA N RGD:5509061 20210520 MGI 1552956 St8sia6 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1552958 Rnase10 ribonuclease, RNase A family, 10 (non-active) gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20200310 MGI PMID:21084446 1552958 Rnase10 ribonuclease, RNase A family, 10 (non-active) gene MP:0001148 enlarged testis IAGP N RGD:5509061 20200310 MGI PMID:21084446 1552958 Rnase10 ribonuclease, RNase A family, 10 (non-active) gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:21084446 1552958 Rnase10 ribonuclease, RNase A family, 10 (non-active) gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20200310 MGI 1552958 Rnase10 ribonuclease, RNase A family, 10 (non-active) gene MP:0001875 testis inflammation IAGP N RGD:5509061 20200310 MGI PMID:21084446 1552958 Rnase10 ribonuclease, RNase A family, 10 (non-active) gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:21084446 1552958 Rnase10 ribonuclease, RNase A family, 10 (non-active) gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20200310 MGI PMID:21084446 1552958 Rnase10 ribonuclease, RNase A family, 10 (non-active) gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20200310 MGI PMID:21084446 1552958 Rnase10 ribonuclease, RNase A family, 10 (non-active) gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20200310 MGI PMID:21084446 1552958 Rnase10 ribonuclease, RNase A family, 10 (non-active) gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20200310 MGI PMID:21084446 1552958 Rnase10 ribonuclease, RNase A family, 10 (non-active) gene MP:0004924 abnormal behavior IEA N RGD:5509061 20200310 MGI 1552958 Rnase10 ribonuclease, RNase A family, 10 (non-active) gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:21084446 1552958 Rnase10 ribonuclease, RNase A family, 10 (non-active) gene MP:0004934 epididymis epithelium degeneration IAGP N RGD:5509061 20200310 MGI PMID:21084446 1552958 Rnase10 ribonuclease, RNase A family, 10 (non-active) gene MP:0009198 abnormal male genitalia morphology IAGP N RGD:5509061 20200310 MGI PMID:21084446 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20191003 MGI PMID:30842416 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191003 MGI PMID:30842416 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20241031 MGI PMID:39194072 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20241031 MGI PMID:39194072 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20241031 MGI PMID:39194072 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0002083 premature death IAGP N RGD:5509061 20191003 MGI PMID:30842416 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20241031 MGI PMID:39194072 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20241031 MGI PMID:39194072 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20191003 MGI PMID:30842416 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0008527 embryonic lethality at implantation IAGP N RGD:5509061 20241031 MGI PMID:39194072 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20241031 MGI PMID:39194072 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20191003 MGI PMID:30842416 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20191003 MGI PMID:30842416 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20241031 MGI PMID:39194072 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0011187 abnormal parietal endoderm morphology IAGP N RGD:5509061 20241031 MGI PMID:39194072 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1552959 Znhit1 zinc finger, HIT domain containing 1 gene MP:0013485 increased Paneth cell number IAGP N RGD:5509061 20191003 MGI PMID:30842416 1552963 Rpl13a ribosomal protein L13A gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20170413 MGI PMID:27820699 1552963 Rpl13a ribosomal protein L13A gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:23460747 1552963 Rpl13a ribosomal protein L13A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23460747 1552963 Rpl13a ribosomal protein L13A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23460747 1552963 Rpl13a ribosomal protein L13A gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20170413 MGI PMID:27820699 1552963 Rpl13a ribosomal protein L13A gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20170413 MGI PMID:27820699 1552963 Rpl13a ribosomal protein L13A gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20170413 MGI PMID:27820699 1552963 Rpl13a ribosomal protein L13A gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20170413 MGI PMID:27820699 1552963 Rpl13a ribosomal protein L13A gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20170413 MGI PMID:27820699 1552963 Rpl13a ribosomal protein L13A gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23460747 1552963 Rpl13a ribosomal protein L13A gene MP:0005426 tachypnea IAGP N RGD:5509061 20141003 MGI PMID:23460747 1552963 Rpl13a ribosomal protein L13A gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23460747 1552963 Rpl13a ribosomal protein L13A gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:23460747 1552963 Rpl13a ribosomal protein L13A gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:23460747 1552963 Rpl13a ribosomal protein L13A gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:23460747 1552963 Rpl13a ribosomal protein L13A gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20170413 MGI PMID:27820699 1552964 Ubr7 ubiquitin protein ligase E3 component n-recognin 7 (putative) gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20240523 MGI 1552964 Ubr7 ubiquitin protein ligase E3 component n-recognin 7 (putative) gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1552964 Ubr7 ubiquitin protein ligase E3 component n-recognin 7 (putative) gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230601 MGI 1552964 Ubr7 ubiquitin protein ligase E3 component n-recognin 7 (putative) gene MP:0002626 increased heart rate IEA N RGD:5509061 20230601 MGI 1552964 Ubr7 ubiquitin protein ligase E3 component n-recognin 7 (putative) gene MP:0002764 short tibia IEA N RGD:5509061 20230601 MGI 1552964 Ubr7 ubiquitin protein ligase E3 component n-recognin 7 (putative) gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230601 MGI 1552964 Ubr7 ubiquitin protein ligase E3 component n-recognin 7 (putative) gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20240523 MGI 1552964 Ubr7 ubiquitin protein ligase E3 component n-recognin 7 (putative) gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20240523 MGI 1552964 Ubr7 ubiquitin protein ligase E3 component n-recognin 7 (putative) gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20240523 MGI 1552964 Ubr7 ubiquitin protein ligase E3 component n-recognin 7 (putative) gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20230601 MGI 1552964 Ubr7 ubiquitin protein ligase E3 component n-recognin 7 (putative) gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20231207 MGI 1552964 Ubr7 ubiquitin protein ligase E3 component n-recognin 7 (putative) gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1552964 Ubr7 ubiquitin protein ligase E3 component n-recognin 7 (putative) gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230601 MGI 1552964 Ubr7 ubiquitin protein ligase E3 component n-recognin 7 (putative) gene MP:0010507 shortened RR interval IEA N RGD:5509061 20230601 MGI 1552965 Ppp1r2 protein phosphatase 1, regulatory inhibitor subunit 2 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20170831 MGI PMID:26558779 1552965 Ppp1r2 protein phosphatase 1, regulatory inhibitor subunit 2 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20170831 MGI PMID:26558779 1552965 Ppp1r2 protein phosphatase 1, regulatory inhibitor subunit 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170831 MGI PMID:26558779 1552967 Calb2 calbindin 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10220453 1552967 Calb2 calbindin 2 gene MP:0001473 reduced long-term potentiation IEA N RGD:5509061 20111116 MGI 1552967 Calb2 calbindin 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1552967 Calb2 calbindin 2 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:9294225 1552967 Calb2 calbindin 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10220453 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0001007 abnormal sympathetic system morphology IAGP N RGD:5509061 20141003 MGI PMID:12160745 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12160745 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10482239 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11585795 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12160745 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0001014 absent superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:10482239 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:10482239 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:11585795 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:12160745 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0001025 abnormal sympathetic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12160745 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:10482239 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:12160745 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:15204970 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10482239 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:11585795 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:10482239 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0009284 abnormal sympathetic neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:10482239 1552970 Gfra3 glial cell line derived neurotrophic factor family receptor alpha 3 gene MP:0009561 superior cervical ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:10482239 1552972 Nle1 notchless homolog 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20200310 MGI PMID:16466971 1552972 Nle1 notchless homolog 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20200310 MGI PMID:16611995 1552972 Nle1 notchless homolog 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20200310 MGI PMID:16611995 1552972 Nle1 notchless homolog 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20200310 MGI PMID:24062412 1552972 Nle1 notchless homolog 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16466971 1552972 Nle1 notchless homolog 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16611995 1552972 Nle1 notchless homolog 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23231322 1552972 Nle1 notchless homolog 1 gene MP:0014242 abnormal ribosome biogenesis IAGP N RGD:5509061 20230615 MGI PMID:24062412 1552973 Hdhd2 haloacid dehalogenase-like hydrolase domain containing 2 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21937600 1552974 Tmem138 transmembrane protein 138 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1552974 Tmem138 transmembrane protein 138 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20201022 MGI 1552974 Tmem138 transmembrane protein 138 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1552974 Tmem138 transmembrane protein 138 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1552974 Tmem138 transmembrane protein 138 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1552974 Tmem138 transmembrane protein 138 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1552975 Zfp579 zinc finger protein 579 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 1552975 Zfp579 zinc finger protein 579 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20220519 MGI 1552978 Cdh11 cadherin 11 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20220519 MGI 1552978 Cdh11 cadherin 11 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 1552978 Cdh11 cadherin 11 gene MP:0000601 small liver IEA N RGD:5509061 20210826 MGI 1552978 Cdh11 cadherin 11 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1552978 Cdh11 cadherin 11 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1552978 Cdh11 cadherin 11 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220519 MGI 1552978 Cdh11 cadherin 11 gene MP:0001147 small testis IEA N RGD:5509061 20220519 MGI 1552978 Cdh11 cadherin 11 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:22284184 1552978 Cdh11 cadherin 11 gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 1552978 Cdh11 cadherin 11 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20221215 MGI 1552978 Cdh11 cadherin 11 gene MP:0001399 hyperactivity IEA N RGD:5509061 20221215 MGI 1552978 Cdh11 cadherin 11 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:10545229 1552978 Cdh11 cadherin 11 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220811 MGI 1552978 Cdh11 cadherin 11 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1552978 Cdh11 cadherin 11 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1552978 Cdh11 cadherin 11 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210826 MGI 1552978 Cdh11 cadherin 11 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20221215 MGI 1552978 Cdh11 cadherin 11 gene MP:0009682 abnormal anterior corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:22284184 1552978 Cdh11 cadherin 11 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1552978 Cdh11 cadherin 11 gene MP:0011496 abnormal head size IEA N RGD:5509061 20220519 MGI 1552978 Cdh11 cadherin 11 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20221215 MGI 1552980 Ston1 stonin 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20161103 MGI PMID:26437238 1552980 Ston1 stonin 1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20161103 MGI PMID:26437238 1552980 Ston1 stonin 1 gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20161103 MGI PMID:26437238 1552980 Ston1 stonin 1 gene MP:0011706 abnormal fibroblast migration IAGP N RGD:5509061 20161103 MGI PMID:26437238 1552982 Trub1 TruB pseudouridine (psi) synthase family member 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 1552982 Trub1 TruB pseudouridine (psi) synthase family member 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1552982 Trub1 TruB pseudouridine (psi) synthase family member 1 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20211021 MGI 1552982 Trub1 TruB pseudouridine (psi) synthase family member 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1552982 Trub1 TruB pseudouridine (psi) synthase family member 1 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 1552983 Il3ra interleukin 3 receptor, alpha chain gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7889941 1552983 Il3ra interleukin 3 receptor, alpha chain gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7727767 1552984 Or2b4 olfactory receptor family 2 subfamily B member 4 gene MP:0001003 abnormal olfactory receptor morphology IAGP N RGD:5509061 20141003 MGI PMID:19923288 1552984 Or2b4 olfactory receptor family 2 subfamily B member 4 gene MP:0001003 abnormal olfactory receptor morphology IAGP N RGD:5509061 20200402 MGI PMID:23688909 1552984 Or2b4 olfactory receptor family 2 subfamily B member 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19923288 1552984 Or2b4 olfactory receptor family 2 subfamily B member 4 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19923288 1552984 Or2b4 olfactory receptor family 2 subfamily B member 4 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20200402 MGI PMID:23688909 1552984 Or2b4 olfactory receptor family 2 subfamily B member 4 gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20150205 MGI PMID:23688909 1552986 Tmem50b transmembrane protein 50B gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20211021 MGI 1552986 Tmem50b transmembrane protein 50B gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200310 MGI 1552986 Tmem50b transmembrane protein 50B gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20211021 MGI 1552991 Ilkap integrin-linked kinase-associated serine/threonine phosphatase 2C gene MP:0003858 enhanced coordination IEA N RGD:5509061 20200310 MGI 1552991 Ilkap integrin-linked kinase-associated serine/threonine phosphatase 2C gene MP:0003982 increased cholesterol level IEA N RGD:5509061 20200310 MGI 1552991 Ilkap integrin-linked kinase-associated serine/threonine phosphatase 2C gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230119 MGI 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:12925600 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11859196 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11859196 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12130536 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:11859196 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:12130536 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:11859196 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:12130536 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:11859196 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:12130536 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:12130536 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12925600 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:11859196 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0002989 small kidney IAGP N RGD:5509061 20170126 MGI PMID:17264314 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:12130536 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:12925600 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:12925600 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:12925600 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20170126 MGI PMID:17264314 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:12130536 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:18697905 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0004755 abnormal loop of Henle morphology IAGP N RGD:5509061 20141003 MGI PMID:11859196 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0004757 abnormal distal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12925600 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0004899 absent temporal bone squamous part IAGP N RGD:5509061 20141003 MGI PMID:18697905 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20170126 MGI PMID:17264314 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20170126 MGI PMID:17264314 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:12925600 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20170126 MGI PMID:17264314 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:12925600 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12130536 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20170126 MGI PMID:17264314 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:12130536 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:12130536 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12130536 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11859196 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12130536 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12925600 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11859196 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0011345 truncated loop of Henle IAGP N RGD:5509061 20141003 MGI PMID:12925600 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12925600 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12925600 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0030111 absent temporomandibular joint IAGP N RGD:5509061 20171207 MGI PMID:18697905 1552994 Pou3f3 POU domain, class 3, transcription factor 3 gene MP:0030394 abnormal incus short process morphology IAGP N RGD:5509061 20171207 MGI PMID:18697905 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0000434 megacephaly IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0000445 short snout IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001314 cornea opacity IEA N RGD:5509061 20201022 MGI 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0004380 short frontal bone IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0012175 flat face IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20170223 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:27212239 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552997 Tmco1 transmembrane and coiled-coil domains 1 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220721 MGI PMID:29467381 1552999 Ppp1r9a protein phosphatase 1, regulatory subunit 9A gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16600521 1552999 Ppp1r9a protein phosphatase 1, regulatory subunit 9A gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16600521 1552999 Ppp1r9a protein phosphatase 1, regulatory subunit 9A gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:16600521 1552999 Ppp1r9a protein phosphatase 1, regulatory subunit 9A gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:16600521 1552999 Ppp1r9a protein phosphatase 1, regulatory subunit 9A gene MP:0014378 increased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:16600521 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:19419305 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:11745639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:18806225 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20200310 MGI PMID:7840851 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000549 absent limbs IAGP N RGD:5509061 20200310 MGI PMID:2884254 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000578 ulcerated autopod IAGP N RGD:5509061 20200310 MGI PMID:18806225 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:18806225 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20200310 MGI PMID:8118868 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000706 small thymus IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000706 small thymus IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:27670070 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:11745639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20200310 MGI PMID:11745639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20200310 MGI PMID:11745639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20200310 MGI PMID:11745639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20200310 MGI PMID:11745639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:11745639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:664185 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001189 absent skin pigmentation IAGP N RGD:5509061 20200310 MGI PMID:7840851 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20200310 MGI PMID:16860389 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20200310 MGI PMID:2884254 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001193 psoriasis IAGP N RGD:5509061 20200310 MGI PMID:19419305 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20200310 MGI PMID:7840851 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001212 skin lesions IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001212 skin lesions IAGP N RGD:5509061 20200310 MGI PMID:664185 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:11745639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:2884254 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:16860389 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:664185 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200310 MGI PMID:16505059 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20200310 MGI PMID:16505059 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20200310 MGI PMID:22724066 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:7840851 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001846 increased inflammatory response IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:18806225 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:664185 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20200310 MGI PMID:6380298 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20200310 MGI PMID:18806225 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:664185 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:2884254 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:6380298 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002145 abnormal T cell differentiation IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:11745639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002221 abnormal lymph organ size IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:18806225 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20200310 MGI PMID:3551623 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:1756226 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:6334306 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002491 decreased IgD level IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:18806225 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:2884254 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:9586639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20200310 MGI PMID:7840851 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:11145649 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20200310 MGI PMID:18806225 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0003201 extremity edema IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20200310 MGI PMID:11145649 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20200310 MGI PMID:7840851 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20200310 MGI PMID:11745639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20200310 MGI PMID:664185 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20200310 MGI PMID:2884254 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20200310 MGI PMID:16505059 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20200310 MGI PMID:16505059 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20200310 MGI PMID:19419305 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20200310 MGI PMID:11145649 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20200310 MGI PMID:18806225 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0004944 abnormal B cell negative selection IAGP N RGD:5509061 20200310 MGI PMID:9586639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0004978 decreased B-1 B cell number IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:16860389 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:11145649 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20200310 MGI PMID:3891855 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008126 increased dendritic cell number IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20200310 MGI PMID:9586639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20200310 MGI PMID:17600736 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20200310 MGI PMID:18806225 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20200310 MGI PMID:3891855 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008215 decreased immature B cell number IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:18806225 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20200310 MGI PMID:11745639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200310 MGI PMID:16505059 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:16505059 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200310 MGI PMID:16505059 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200310 MGI PMID:16505059 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20200310 MGI PMID:16505059 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200310 MGI PMID:16505059 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20200310 MGI PMID:19419305 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20200310 MGI PMID:14987753 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:2884254 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:18806225 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20200310 MGI PMID:19419305 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20200310 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20200310 MGI PMID:11745639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11745639 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:1184950 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0011130 absent tertiary ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:21435452 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200310 MGI PMID:16505059 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200310 MGI PMID:16505059 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20200310 MGI PMID:14987753 1553000 Ptpn6 protein tyrosine phosphatase, non-receptor type 6 gene MP:0031234 increased circulating serum amyloid protein level IAGP N RGD:5509061 20210225 MGI PMID:21435452 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11138930 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18160655 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:16850391 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:6315811 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:6315811 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9950794 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20007718 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:21896731 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:7202025 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000745 tremors IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000745 tremors IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:21303697 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:11530237 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12692847 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:24391715 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:12692847 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:18160655 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000867 abnormal cerebellum anterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:12528192 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000869 abnormal cerebellum posterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:12528192 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12528192 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12692847 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15071184 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:20007718 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21303697 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22869680 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20171207 MGI PMID:21856732 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20180201 MGI PMID:11504598 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:11530237 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:12528192 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:15071184 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:21896731 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:6315811 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:11138930 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:21303697 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:22869680 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20171207 MGI PMID:21856732 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11530237 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:24391715 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:16850391 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16850391 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21896731 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22869680 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24391715 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15071184 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18160655 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19056848 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20007718 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21303697 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21896731 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22869680 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:7202025 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:9950794 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20171207 MGI PMID:21856732 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20007718 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:22163015 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:11984826 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20007718 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21896731 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:7202025 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22869680 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18160655 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20007718 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21303697 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22869680 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20171207 MGI PMID:21856732 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:22869680 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20171207 MGI PMID:21856732 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:21896731 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001866 nasal inflammation IAGP N RGD:5509061 20141003 MGI PMID:24391715 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001921 reduced fertility IEA N RGD:5509061 20111116 MGI 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:11984826 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16850391 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:11984826 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:20007718 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:9950794 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12528192 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15071184 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15790756 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17314284 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18160655 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19056848 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20007718 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21303697 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21896731 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22869680 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7202025 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002083 premature death IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002083 premature death IAGP N RGD:5509061 20171207 MGI PMID:21856732 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002083 premature death IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15071184 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20171207 MGI PMID:21856732 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:18160655 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:24391715 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:9950794 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22869680 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:24391715 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15790756 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16850391 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11138930 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:15790756 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:9950794 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17314284 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:24391715 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20141003 MGI PMID:11138930 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20141003 MGI PMID:12692847 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:20007718 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21303697 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22869680 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:24391715 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20171207 MGI PMID:21856732 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17314284 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003947 abnormal cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:6315811 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11138930 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18160655 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20007718 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21896731 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20191226 MGI PMID:16850391 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20141003 MGI PMID:6315811 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0004781 abnormal surfactant composition IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0004894 uterus atrophy IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0005138 decreased prolactin level IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11138930 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:6257302 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:24391715 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:22869680 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20171207 MGI PMID:21856732 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0005499 abnormal olfactory system morphology IAGP N RGD:5509061 20141003 MGI PMID:24391715 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0005544 cornea deposits IAGP N RGD:5509061 20141003 MGI PMID:22163015 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16850391 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:22869680 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:9950794 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20190124 MGI PMID:15644330 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20190124 MGI PMID:15644330 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:24391715 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008257 thin myometrium IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008258 thin endometrium IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:12692847 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008332 decreased lactotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008365 adenohypophysis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:24391715 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:16850391 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12692847 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008570 lipidosis IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008570 lipidosis IAGP N RGD:5509061 20141003 MGI PMID:6257302 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20180201 MGI PMID:12528192 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24391715 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:20007718 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:22869680 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:24391715 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20171207 MGI PMID:21856732 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009081 thin uterus IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009096 decreased endometrial gland number IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:16850391 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20141003 MGI PMID:16850391 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009287 decreased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009359 endometrium atrophy IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009587 abnormal plasma membrane sphingolipid content IAGP N RGD:5509061 20141003 MGI PMID:6315811 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009588 increased plasma membrane sphingolipid content IAGP N RGD:5509061 20141003 MGI PMID:6315811 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009589 sphingomyelinosis IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009589 sphingomyelinosis IAGP N RGD:5509061 20141003 MGI PMID:6315811 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009589 sphingomyelinosis IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009841 foam cell reticulosis IAGP N RGD:5509061 20141003 MGI PMID:20007718 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0009841 foam cell reticulosis IAGP N RGD:5509061 20141003 MGI PMID:21896731 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11984826 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15071184 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21896731 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:6315811 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:11504598 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:18160655 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20171207 MGI PMID:21856732 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010052 increased grip strength IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010161 decreased brain cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11138930 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010161 decreased brain cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18160655 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010162 increased brain cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21303697 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010162 increased brain cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010162 increased brain cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22869680 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010162 increased brain cholesterol level IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010162 increased brain cholesterol level IAGP N RGD:5509061 20171207 MGI PMID:21856732 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010162 increased brain cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:11138930 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010162 increased brain cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:20007718 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:19056848 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010762 abnormal microglial cell activation IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010815 enlarged alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0010998 pulmonary alveolar proteinosis IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20190124 MGI PMID:15644330 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20190124 MGI PMID:15644330 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0011637 abnormal mitochondrial matrix morphology IAGP N RGD:5509061 20190124 MGI PMID:15644330 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20190117 MGI PMID:15465426 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:9950794 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0012230 abnormal sphingolipid level IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20150709 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0012315 impaired learning IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20180201 MGI PMID:28379564 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0014270 decreased ovary secretion IAGP N RGD:5509061 20230810 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:11530237 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0014330 abnormal Purkinje cell focal axonal swelling IAGP N RGD:5509061 20240118 MGI PMID:12528192 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0014460 increased lipid level IAGP N RGD:5509061 20240704 MGI PMID:23843985 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0014460 increased lipid level IAGP N RGD:5509061 20240704 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20240704 MGI PMID:19056848 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0020582 increased ceramide level IAGP N RGD:5509061 20190926 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0020582 increased ceramide level IAGP N RGD:5509061 20240704 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:16850391 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:28167839 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:15105438 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0031560 decreased ganglioside level IAGP N RGD:5509061 20240704 MGI PMID:19056848 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0031561 increased ganglioside level IAGP N RGD:5509061 20240704 MGI PMID:19056848 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0031561 increased ganglioside level IAGP N RGD:5509061 20240704 MGI PMID:22048958 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0031561 increased ganglioside level IAGP N RGD:5509061 20240704 MGI PMID:26019327 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0031632 increased lung cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:18160655 1553002 Npc1 NPC intracellular cholesterol transporter 1 gene MP:0031632 increased lung cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:23843985 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20200116 MGI PMID:30808746 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170713 MGI PMID:26344103 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200116 MGI PMID:30808746 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200116 MGI PMID:30808746 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20170713 MGI PMID:26344103 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20170713 MGI PMID:26344103 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20170713 MGI PMID:26344103 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20170713 MGI PMID:26344103 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20200116 MGI PMID:30808746 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200116 MGI PMID:30808746 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200116 MGI PMID:30808746 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20170713 MGI PMID:26344103 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20200116 MGI PMID:30808746 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20200116 MGI PMID:30808746 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20170713 MGI PMID:26344103 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20170713 MGI PMID:26344103 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20200116 MGI PMID:30808746 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20170713 MGI PMID:26344103 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20170713 MGI PMID:26344103 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20200116 MGI PMID:30808746 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:30808746 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200116 MGI PMID:30808746 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20170713 MGI PMID:26344103 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20170713 MGI PMID:26344103 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20170713 MGI PMID:26344103 1553003 Mpc1 mitochondrial pyruvate carrier 1 gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20200116 MGI PMID:30808746 1553005 Trim31 tripartite motif-containing 31 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:27929086 1553005 Trim31 tripartite motif-containing 31 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20200310 MGI PMID:27929086 1553005 Trim31 tripartite motif-containing 31 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20200310 MGI PMID:27929086 1553005 Trim31 tripartite motif-containing 31 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20200310 MGI PMID:27929086 1553005 Trim31 tripartite motif-containing 31 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20200310 MGI PMID:27929086 1553005 Trim31 tripartite motif-containing 31 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20200310 MGI PMID:27929086 1553005 Trim31 tripartite motif-containing 31 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1553005 Trim31 tripartite motif-containing 31 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20200310 MGI PMID:27929086 1553005 Trim31 tripartite motif-containing 31 gene MP:0013022 increased Ly6C high monocyte number IAGP N RGD:5509061 20200310 MGI PMID:27929086 1553007 Jph4 junctophilin 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:16809425 1553007 Jph4 junctophilin 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:16809425 1553007 Jph4 junctophilin 4 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20200310 MGI PMID:16809425 1553007 Jph4 junctophilin 4 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20200310 MGI PMID:16809425 1553007 Jph4 junctophilin 4 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:16809425 1553007 Jph4 junctophilin 4 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20200310 MGI PMID:26929330 1553007 Jph4 junctophilin 4 gene MP:0001924 infertility IAGP N RGD:5509061 20200310 MGI PMID:16809425 1553007 Jph4 junctophilin 4 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20200310 MGI PMID:16809425 1553007 Jph4 junctophilin 4 gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20200310 MGI PMID:16809425 1553007 Jph4 junctophilin 4 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20200310 MGI PMID:16809425 1553007 Jph4 junctophilin 4 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20200310 MGI PMID:16809425 1553007 Jph4 junctophilin 4 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20200310 MGI PMID:26929330 1553007 Jph4 junctophilin 4 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20200310 MGI PMID:16809425 1553007 Jph4 junctophilin 4 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20200310 MGI PMID:26929330 1553007 Jph4 junctophilin 4 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16809425 1553007 Jph4 junctophilin 4 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:16809425 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000160 kyphosis IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000414 alopecia IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000440 domed cranium IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000467 abnormal esophagus morphology IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17878299 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000524 decreased renal tubule number IAGP N RGD:5509061 20141003 MGI PMID:23555292 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17878299 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000829 dilated fourth ventricle IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000917 obstructive hydrocephaly IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:11584271 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001192 scaly skin IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001194 dermatitis IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001219 thick epidermis IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001406 abnormal gait IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:11559594 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:11559594 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11559594 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11584271 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:11559594 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0002083 premature death IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11559594 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151112 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17878299 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17878299 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:17878299 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0002958 cerebral aqueductal stenosis IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0003354 astrocytosis IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23555292 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:17878299 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0003853 dry skin IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11584271 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:11584271 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11559594 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11584271 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:23555292 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0004548 dilated esophagus IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:11584271 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0004947 skin inflammation IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:17878299 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17878299 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0005202 lethargy IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0005238 increased brain size IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0006323 abnormal extraembryonic mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:11559594 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17878299 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17878299 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0008638 increased circulating interleukin-1 alpha level IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20190516 MGI PMID:28779153 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0011057 absent brain ependyma motile cilia IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11559594 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11584271 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11584271 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0011202 abnormal ectoplacental cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:11559594 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0011518 abnormal cell chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:11584271 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:11584271 1553011 Wasl WASP like actin nucleation promoting factor gene MP:0012003 abnormal septum of telencephalon morphology IAGP N RGD:5509061 20151008 MGI PMID:24462670 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000033 absent scala media IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000041 absent endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000777 increased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:19279136 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19279136 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:19279136 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0001066 absent trigeminal nerve IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16847871 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0003146 absent cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0003165 absent superior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0003543 abnormal vascular endothelial cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0003740 fusion of middle ear ossicles IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20141003 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0004096 abnormal midbrain-hindbrain boundary development IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0004315 absent vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0004330 abnormal vestibular saccular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0004443 absent supraoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0004568 fusion of glossopharyngeal and vagus nerve IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0004592 small mandible IAGP N RGD:5509061 20170921 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0004923 absent common crus IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0006287 inner ear cyst IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0006289 otic capsule hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0006293 absent nasal placodes IAGP N RGD:5509061 20141003 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0006294 absent optic vesicle IAGP N RGD:5509061 20141003 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0009843 decreased neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0009845 abnormal neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:9247335 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20141003 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0012170 absent optic placodes IAGP N RGD:5509061 20141003 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0012176 abnormal head development IAGP N RGD:5509061 20141003 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0012706 decreased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12367504 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0012800 abnormal rhombomere 5 morphology IAGP N RGD:5509061 20141003 MGI PMID:15829521 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0013906 absent embryonic telencephalon IAGP N RGD:5509061 20150924 MGI PMID:11731459 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0030124 middle ear ossicle hypoplasia IAGP N RGD:5509061 20171005 MGI PMID:15996652 1553014 Gbx2 gastrulation brain homeobox 2 gene MP:0030322 styloid process hypoplasia IAGP N RGD:5509061 20171109 MGI PMID:15996652 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20200310 MGI PMID:21183657 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200310 MGI PMID:21183657 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0001314 cornea opacity IEA N RGD:5509061 20220811 MGI 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:12447384 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20200310 MGI PMID:21183657 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20200310 MGI PMID:21183657 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:12447384 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20200310 MGI PMID:12447384 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20200310 MGI PMID:12447384 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20200310 MGI PMID:21183657 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0003087 absent allantois IAGP N RGD:5509061 20200310 MGI PMID:12447384 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20200310 MGI PMID:21183657 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0005030 absent amnion IAGP N RGD:5509061 20200310 MGI PMID:12447384 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0005163 cyclopia IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20200310 MGI PMID:12447384 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21183657 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0008384 absent nasal capsule IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20200310 MGI PMID:21183657 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0009593 absent chorion IAGP N RGD:5509061 20200310 MGI PMID:12447384 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0010287 increased reproductive system tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21183657 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20200310 MGI PMID:21183657 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0010335 fused first pharyngeal arch IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0010406 common atrium IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0010432 common ventricle IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20200310 MGI PMID:12447384 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12447384 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20200310 MGI PMID:12447384 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0012084 truncated foregut IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20200310 MGI PMID:12447384 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0013906 absent embryonic telencephalon IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553015 Pcsk6 proprotein convertase subtilisin/kexin type 6 gene MP:0030268 agnathia IAGP N RGD:5509061 20200310 MGI PMID:10809672 1553016 Pdlim2 PDZ and LIM domain 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15963787 1553016 Pdlim2 PDZ and LIM domain 2 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:15963787 1553016 Pdlim2 PDZ and LIM domain 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15963787 1553017 Pno1 partner of NOB1 homolog gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:23029399 1553017 Pno1 partner of NOB1 homolog gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23029399 1553018 Zdhhc20 zinc finger, DHHC domain containing 20 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20201022 MGI 1553018 Zdhhc20 zinc finger, DHHC domain containing 20 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20240905 MGI PMID:38733589 1553018 Zdhhc20 zinc finger, DHHC domain containing 20 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20201022 MGI 1553018 Zdhhc20 zinc finger, DHHC domain containing 20 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20210520 MGI 1553018 Zdhhc20 zinc finger, DHHC domain containing 20 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240905 MGI PMID:38733589 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20200310 MGI PMID:4448900 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20200310 MGI PMID:4448900 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20200310 MGI PMID:6736600 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20200310 MGI PMID:4448900 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20200310 MGI PMID:4448900 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0000371 diluted coat color IAGP N RGD:5509061 20200310 MGI PMID:12647238 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0000371 diluted coat color IAGP N RGD:5509061 20200310 MGI PMID:4448900 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:19436707 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0001265 decreased body size IEA N RGD:5509061 20200310 MGI 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:12647238 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:4448900 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:4448900 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0001923 reduced female fertility IEA N RGD:5509061 20200310 MGI 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0001925 male infertility IEA N RGD:5509061 20200310 MGI 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20200310 MGI PMID:4448900 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200310 MGI PMID:4448900 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20200310 MGI PMID:19436707 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:6736600 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20200310 MGI PMID:4448900 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20200310 MGI PMID:4448900 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20200310 MGI PMID:15109702 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20200310 MGI PMID:4448900 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0002978 absent otoliths IAGP N RGD:5509061 20200310 MGI PMID:6736600 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0003173 decreased lysosomal enzyme secretion IAGP N RGD:5509061 20200310 MGI PMID:1912584 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20200310 MGI PMID:15537701 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0003889 enhanced sensorimotor gating IAGP N RGD:5509061 20200310 MGI PMID:10586974 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0004721 abnormal platelet dense granule morphology IAGP N RGD:5509061 20200310 MGI PMID:1912584 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20200310 MGI PMID:1912584 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:10586974 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:1912584 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20200310 MGI PMID:15109702 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20200310 MGI PMID:16235133 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20200310 MGI PMID:2778559 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20200310 MGI PMID:4448900 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0005191 head tilt IAGP N RGD:5509061 20200310 MGI PMID:4448900 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:1912584 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20200310 MGI PMID:1912584 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20200310 MGI PMID:9585243 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20200310 MGI PMID:10586974 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20200310 MGI PMID:1912584 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0009617 decreased brain zinc level IAGP N RGD:5509061 20240912 MGI PMID:9697856 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20200310 MGI PMID:20664521 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:4448900 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20200310 MGI 1553020 Ap3d1 adaptor-related protein complex 3, delta 1 subunit gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20200310 MGI PMID:1912584 1553023 Nutf2 nuclear transport factor 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1553023 Nutf2 nuclear transport factor 2 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1553023 Nutf2 nuclear transport factor 2 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1553023 Nutf2 nuclear transport factor 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553026 Ssh3 slingshot protein phosphatase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18442045 1553027 Spef2 sperm flagellar 2 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0001872 sinus inflammation IAGP N RGD:5509061 20141003 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20141003 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0030316 enlarged neurocranium IAGP N RGD:5509061 20171109 MGI PMID:21715716 1553027 Spef2 sperm flagellar 2 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20220224 MGI PMID:21715716 1553028 Cnot10 CCR4-NOT transcription complex, subunit 10 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1553028 Cnot10 CCR4-NOT transcription complex, subunit 10 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1553028 Cnot10 CCR4-NOT transcription complex, subunit 10 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1553028 Cnot10 CCR4-NOT transcription complex, subunit 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553029 Klk11 kallikrein related-peptidase 11 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20210826 MGI 1553029 Klk11 kallikrein related-peptidase 11 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1553029 Klk11 kallikrein related-peptidase 11 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1553029 Klk11 kallikrein related-peptidase 11 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1553029 Klk11 kallikrein related-peptidase 11 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1553029 Klk11 kallikrein related-peptidase 11 gene MP:0001192 scaly skin IAGP N RGD:5509061 20240404 MGI PMID:36689511 1553029 Klk11 kallikrein related-peptidase 11 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20240404 MGI PMID:36689511 1553029 Klk11 kallikrein related-peptidase 11 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1553029 Klk11 kallikrein related-peptidase 11 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1553029 Klk11 kallikrein related-peptidase 11 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20210128 MGI 1553029 Klk11 kallikrein related-peptidase 11 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230601 MGI 1553030 Thbd thrombomodulin gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11557684 1553030 Thbd thrombomodulin gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:9576763 1553030 Thbd thrombomodulin gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:7846065 1553030 Thbd thrombomodulin gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11557684 1553030 Thbd thrombomodulin gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9576763 1553030 Thbd thrombomodulin gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11557684 1553030 Thbd thrombomodulin gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:9576763 1553030 Thbd thrombomodulin gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:12579195 1553030 Thbd thrombomodulin gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:12579195 1553030 Thbd thrombomodulin gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:12579195 1553030 Thbd thrombomodulin gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12579195 1553030 Thbd thrombomodulin gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:7846065 1553030 Thbd thrombomodulin gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:8575060 1553030 Thbd thrombomodulin gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7846065 1553030 Thbd thrombomodulin gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11557684 1553030 Thbd thrombomodulin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7846065 1553030 Thbd thrombomodulin gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:22573811 1553030 Thbd thrombomodulin gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:12208873 1553030 Thbd thrombomodulin gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:11557684 1553030 Thbd thrombomodulin gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:12579195 1553030 Thbd thrombomodulin gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:12208873 1553030 Thbd thrombomodulin gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12579195 1553030 Thbd thrombomodulin gene MP:0003415 priapism IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:12208873 1553030 Thbd thrombomodulin gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0003913 increased heart right ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:7846065 1553030 Thbd thrombomodulin gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12579195 1553030 Thbd thrombomodulin gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0005161 hematuria IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:21885846 1553030 Thbd thrombomodulin gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22573811 1553030 Thbd thrombomodulin gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:10233896 1553030 Thbd thrombomodulin gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:21885846 1553030 Thbd thrombomodulin gene MP:0005630 increased lung weight IEA N RGD:5509061 20220811 MGI 1553030 Thbd thrombomodulin gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:12208873 1553030 Thbd thrombomodulin gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:11557684 1553030 Thbd thrombomodulin gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22573811 1553030 Thbd thrombomodulin gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22573811 1553030 Thbd thrombomodulin gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:11557684 1553030 Thbd thrombomodulin gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:22573811 1553030 Thbd thrombomodulin gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:11557684 1553030 Thbd thrombomodulin gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:12208873 1553030 Thbd thrombomodulin gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:11557684 1553030 Thbd thrombomodulin gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12208873 1553030 Thbd thrombomodulin gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:9576763 1553030 Thbd thrombomodulin gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11557684 1553030 Thbd thrombomodulin gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12208873 1553030 Thbd thrombomodulin gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22573811 1553030 Thbd thrombomodulin gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22573811 1553030 Thbd thrombomodulin gene MP:0010211 abnormal acute phase protein level IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8575060 1553030 Thbd thrombomodulin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12579195 1553030 Thbd thrombomodulin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7846065 1553030 Thbd thrombomodulin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553030 Thbd thrombomodulin gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21885846 1553030 Thbd thrombomodulin gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21885846 1553030 Thbd thrombomodulin gene MP:0011514 skin hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:12579195 1553030 Thbd thrombomodulin gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1553030 Thbd thrombomodulin gene MP:0020407 abnormal placental thrombosis IAGP N RGD:5509061 20161124 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:12579195 1553030 Thbd thrombomodulin gene MP:0031083 increased circulating D-dimer level IAGP N RGD:5509061 20200709 MGI PMID:11518727 1553030 Thbd thrombomodulin gene MP:0031083 increased circulating D-dimer level IAGP N RGD:5509061 20200709 MGI PMID:11557684 1553030 Thbd thrombomodulin gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:11557684 1553030 Thbd thrombomodulin gene MP:0031167 abnormal lung thrombosis IAGP N RGD:5509061 20201210 MGI PMID:9576763 1553035 Nrxn3 neurexin III gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:23827676 1553035 Nrxn3 neurexin III gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:14983056 1553035 Nrxn3 neurexin III gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:12827191 1553035 Nrxn3 neurexin III gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12827191 1553035 Nrxn3 neurexin III gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12827191 1553035 Nrxn3 neurexin III gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111215 MGI 1553035 Nrxn3 neurexin III gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12827191 1553035 Nrxn3 neurexin III gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:14983056 1553035 Nrxn3 neurexin III gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12827191 1553035 Nrxn3 neurexin III gene MP:0002915 abnormal synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:12827191 1553035 Nrxn3 neurexin III gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:12827191 1553035 Nrxn3 neurexin III gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:12827191 1553035 Nrxn3 neurexin III gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23827676 1553035 Nrxn3 neurexin III gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:12827191 1553035 Nrxn3 neurexin III gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:12827191 1553035 Nrxn3 neurexin III gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:23827676 1553035 Nrxn3 neurexin III gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12827191 1553035 Nrxn3 neurexin III gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12827191 1553035 Nrxn3 neurexin III gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12827191 1553035 Nrxn3 neurexin III gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:12827191 1553035 Nrxn3 neurexin III gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20180301 MGI PMID:23827676 1553036 Acy3 aminoacylase 3 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1553036 Acy3 aminoacylase 3 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20220811 MGI 1553036 Acy3 aminoacylase 3 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1553036 Acy3 aminoacylase 3 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1553036 Acy3 aminoacylase 3 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1553039 Chst15 carbohydrate sulfotransferase 15 gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20439988 1553039 Chst15 carbohydrate sulfotransferase 15 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:20439988 1553041 Rbm25 RNA binding motif protein 25 gene MP:0001293 anophthalmia IEA N RGD:5509061 20201231 MGI 1553041 Rbm25 RNA binding motif protein 25 gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 1553041 Rbm25 RNA binding motif protein 25 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1553041 Rbm25 RNA binding motif protein 25 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553041 Rbm25 RNA binding motif protein 25 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1553045 Numa1 nuclear mitotic apparatus protein 1 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20200310 MGI PMID:19255246 1553045 Numa1 nuclear mitotic apparatus protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19255246 1553045 Numa1 nuclear mitotic apparatus protein 1 gene MP:0011705 absent fibroblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:19255246 1553051 Clec4f C-type lectin domain family 4, member f gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:23762286 1553051 Clec4f C-type lectin domain family 4, member f gene MP:0011072 abnormal macrophage cytokine production IAGP N RGD:5509061 20200310 MGI PMID:23762286 1553053 Phf21b PHD finger protein 21B gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20220929 MGI PMID:35866480 1553053 Phf21b PHD finger protein 21B gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20220929 MGI PMID:35866480 1553053 Phf21b PHD finger protein 21B gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20220929 MGI PMID:35866480 1553053 Phf21b PHD finger protein 21B gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20220929 MGI PMID:35866480 1553053 Phf21b PHD finger protein 21B gene MP:0012066 decreased astrocyte number IAGP N RGD:5509061 20220929 MGI PMID:35866480 1553053 Phf21b PHD finger protein 21B gene MP:0020514 abnormal dendritic thin spine morphology IAGP N RGD:5509061 20220929 MGI PMID:35866480 1553053 Phf21b PHD finger protein 21B gene MP:0021112 impaired social recognition IAGP N RGD:5509061 20220929 MGI PMID:35866480 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22110650 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20170223 MGI PMID:27143553 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20170223 MGI PMID:27143553 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20170223 MGI PMID:27143553 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20170223 MGI PMID:27143553 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0008448 abnormal retina cone cell inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0008455 abnormal retina rod cell inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20170223 MGI PMID:27143553 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20170223 MGI PMID:27143553 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20240404 MGI PMID:21349921 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20170223 MGI PMID:27143553 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0030973 impaired gluconeogenesis IAGP N RGD:5509061 20200102 MGI PMID:27143553 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:27143553 1553055 C1qtnf5 C1q and tumor necrosis factor related protein 5 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:21349921 1553057 Slc25a26 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 26 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14504232 1553057 Slc25a26 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 26 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14504232 1553058 Slc17a2 solute carrier family 17 (sodium phosphate), member 2 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210128 MGI 1553058 Slc17a2 solute carrier family 17 (sodium phosphate), member 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1553059 Nanog Nanog homeobox gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:12787504 1553059 Nanog Nanog homeobox gene MP:0002583 absent extraembryonic ectoderm IAGP N RGD:5509061 20141003 MGI PMID:12787504 1553059 Nanog Nanog homeobox gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:20435031 1553059 Nanog Nanog homeobox gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20435031 1553059 Nanog Nanog homeobox gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12787504 1553059 Nanog Nanog homeobox gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20435031 1553059 Nanog Nanog homeobox gene MP:0011184 absent embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:12787504 1553059 Nanog Nanog homeobox gene MP:0011185 absent primitive endoderm IAGP N RGD:5509061 20141003 MGI PMID:20435031 1553060 Gphb5 glycoprotein hormone beta 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15699348 1553060 Gphb5 glycoprotein hormone beta 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16210345 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0004089 dilated sarcoplasmic reticulum IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0004937 dilated heart IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0009777 abnormal behavioral response to anesthetic IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0010052 increased grip strength IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0010394 decreased QRS amplitude IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0010520 sinoatrial block IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0011634 abnormal mitochondrial inner membrane morphology IAGP N RGD:5509061 20150910 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0014390 decreased myocardial fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:25506927 1553062 Mto1 mitochondrial tRNA translation optimization 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:25506927 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230119 MGI 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20200310 MGI PMID:30485550 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20200310 MGI PMID:30485550 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20230119 MGI 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20230119 MGI 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20200310 MGI PMID:30485550 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230119 MGI 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210128 MGI 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20210128 MGI 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20230119 MGI 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20200310 MGI PMID:30485550 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20220519 MGI 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200310 MGI PMID:30485550 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1553063 Nsun5 NOL1/NOP2/Sun domain family, member 5 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1553064 Fasl Fas ligand gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20200310 MGI PMID:15980239 1553064 Fasl Fas ligand gene MP:0000599 enlarged liver IAGP N RGD:5509061 20200310 MGI PMID:14764677 1553064 Fasl Fas ligand gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:16118350 1553064 Fasl Fas ligand gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20200310 MGI PMID:14764677 1553064 Fasl Fas ligand gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:14764677 1553064 Fasl Fas ligand gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:14764677 1553064 Fasl Fas ligand gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:16935260 1553064 Fasl Fas ligand gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:21479271 1553064 Fasl Fas ligand gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:14764677 1553064 Fasl Fas ligand gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:16935260 1553064 Fasl Fas ligand gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:21479271 1553064 Fasl Fas ligand gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:23577189 1553064 Fasl Fas ligand gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20200310 MGI PMID:16935260 1553064 Fasl Fas ligand gene MP:0000921 demyelination IAGP N RGD:5509061 20200310 MGI PMID:9736651 1553064 Fasl Fas ligand gene MP:0001194 dermatitis IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:16935260 1553064 Fasl Fas ligand gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20200310 MGI PMID:17803905 1553064 Fasl Fas ligand gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20200310 MGI PMID:20053716 1553064 Fasl Fas ligand gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20200310 MGI PMID:16118350 1553064 Fasl Fas ligand gene MP:0001786 skin edema IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20200310 MGI 1553064 Fasl Fas ligand gene MP:0001805 decreased IgG level IEA N RGD:5509061 20200310 MGI 1553064 Fasl Fas ligand gene MP:0001844 autoimmune response IAGP N RGD:5509061 20200310 MGI PMID:14764677 1553064 Fasl Fas ligand gene MP:0001847 brain inflammation IAGP N RGD:5509061 20200310 MGI PMID:9736651 1553064 Fasl Fas ligand gene MP:0001851 eye inflammation IAGP N RGD:5509061 20200310 MGI PMID:15980239 1553064 Fasl Fas ligand gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20200310 MGI PMID:23577189 1553064 Fasl Fas ligand gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200310 MGI PMID:16118350 1553064 Fasl Fas ligand gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0001863 blood vessel inflammation IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:14764677 1553064 Fasl Fas ligand gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:16935260 1553064 Fasl Fas ligand gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:16935260 1553064 Fasl Fas ligand gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:3009614 1553064 Fasl Fas ligand gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:3856256 1553064 Fasl Fas ligand gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:14764677 1553064 Fasl Fas ligand gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20200310 MGI PMID:14764677 1553064 Fasl Fas ligand gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:14764677 1553064 Fasl Fas ligand gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:15980239 1553064 Fasl Fas ligand gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:3009614 1553064 Fasl Fas ligand gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0002493 increased IgG level IAGP N RGD:5509061 20200310 MGI PMID:14764677 1553064 Fasl Fas ligand gene MP:0002493 increased IgG level IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0002493 increased IgG level IAGP N RGD:5509061 20200310 MGI PMID:16935260 1553064 Fasl Fas ligand gene MP:0002493 increased IgG level IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:16935260 1553064 Fasl Fas ligand gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:20971954 1553064 Fasl Fas ligand gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0002495 increased IgA level IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0002495 increased IgA level IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0002497 increased IgE level IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20200310 MGI PMID:14764677 1553064 Fasl Fas ligand gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:16118350 1553064 Fasl Fas ligand gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20200310 MGI PMID:14764677 1553064 Fasl Fas ligand gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:11567045 1553064 Fasl Fas ligand gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200310 MGI PMID:23577189 1553064 Fasl Fas ligand gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20200310 MGI PMID:21479271 1553064 Fasl Fas ligand gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20200310 MGI PMID:23577189 1553064 Fasl Fas ligand gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0005015 increased T cell number IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0005015 increased T cell number IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0005017 decreased B cell number IEA N RGD:5509061 20200310 MGI 1553064 Fasl Fas ligand gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20200310 MGI PMID:7512035 1553064 Fasl Fas ligand gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:3009614 1553064 Fasl Fas ligand gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:20971954 1553064 Fasl Fas ligand gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20200310 MGI PMID:12045257 1553064 Fasl Fas ligand gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:23577189 1553064 Fasl Fas ligand gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200310 MGI PMID:23577189 1553064 Fasl Fas ligand gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20200310 MGI PMID:23577189 1553064 Fasl Fas ligand gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:20971954 1553064 Fasl Fas ligand gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:15980239 1553064 Fasl Fas ligand gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:15096538 1553064 Fasl Fas ligand gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20200310 MGI PMID:9736651 1553064 Fasl Fas ligand gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20200310 MGI PMID:21479271 1553064 Fasl Fas ligand gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20200310 MGI PMID:21479271 1553064 Fasl Fas ligand gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:3009614 1553064 Fasl Fas ligand gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20200310 MGI PMID:21479271 1553064 Fasl Fas ligand gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:21479271 1553064 Fasl Fas ligand gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20200310 MGI PMID:20971954 1553064 Fasl Fas ligand gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20200310 MGI PMID:20971954 1553064 Fasl Fas ligand gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20220714 MGI PMID:18818293 1553064 Fasl Fas ligand gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20200310 MGI PMID:6693832 1553064 Fasl Fas ligand gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20200310 MGI PMID:3009614 1553064 Fasl Fas ligand gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20200310 MGI PMID:16935260 1553064 Fasl Fas ligand gene MP:0008891 decreased hepatocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:16118350 1553064 Fasl Fas ligand gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20200310 MGI PMID:9834083 1553064 Fasl Fas ligand gene MP:0011402 renal cast IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20200310 MGI PMID:19794494 1553064 Fasl Fas ligand gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:16935260 1553064 Fasl Fas ligand gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20200310 MGI 1553064 Fasl Fas ligand gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:9736651 1553064 Fasl Fas ligand gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20200310 MGI PMID:21479271 1553064 Fasl Fas ligand gene MP:0030603 increased sperm number IAGP N RGD:5509061 20220714 MGI PMID:18818293 1553065 Armc7 armadillo repeat containing 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1553065 Armc7 armadillo repeat containing 7 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1553065 Armc7 armadillo repeat containing 7 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1553066 Msto1 misato 1, mitochondrial distribution and morphology regulator gene MP:0000692 small spleen IEA N RGD:5509061 20220519 MGI 1553066 Msto1 misato 1, mitochondrial distribution and morphology regulator gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1553066 Msto1 misato 1, mitochondrial distribution and morphology regulator gene MP:0001258 decreased body length IEA N RGD:5509061 20200514 MGI 1553066 Msto1 misato 1, mitochondrial distribution and morphology regulator gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20200514 MGI 1553066 Msto1 misato 1, mitochondrial distribution and morphology regulator gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1553066 Msto1 misato 1, mitochondrial distribution and morphology regulator gene MP:0003068 enlarged kidney IEA N RGD:5509061 20220519 MGI 1553066 Msto1 misato 1, mitochondrial distribution and morphology regulator gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200514 MGI 1553066 Msto1 misato 1, mitochondrial distribution and morphology regulator gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1553072 Mars2 methionine-tRNA synthetase 2 (mitochondrial) gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20200310 MGI 1553072 Mars2 methionine-tRNA synthetase 2 (mitochondrial) gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1553072 Mars2 methionine-tRNA synthetase 2 (mitochondrial) gene MP:0001698 decreased embryo size IEA N RGD:5509061 20200310 MGI 1553072 Mars2 methionine-tRNA synthetase 2 (mitochondrial) gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20200310 MGI 1553072 Mars2 methionine-tRNA synthetase 2 (mitochondrial) gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20200310 MGI 1553072 Mars2 methionine-tRNA synthetase 2 (mitochondrial) gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20221215 MGI 1553072 Mars2 methionine-tRNA synthetase 2 (mitochondrial) gene MP:0009331 absent primitive node IEA N RGD:5509061 20200310 MGI 1553072 Mars2 methionine-tRNA synthetase 2 (mitochondrial) gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20221215 MGI 1553072 Mars2 methionine-tRNA synthetase 2 (mitochondrial) gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1553072 Mars2 methionine-tRNA synthetase 2 (mitochondrial) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553072 Mars2 methionine-tRNA synthetase 2 (mitochondrial) gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20200310 MGI 1553072 Mars2 methionine-tRNA synthetase 2 (mitochondrial) gene MP:0012724 absent head fold IEA N RGD:5509061 20200310 MGI 1553072 Mars2 methionine-tRNA synthetase 2 (mitochondrial) gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1553072 Mars2 methionine-tRNA synthetase 2 (mitochondrial) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20200310 MGI 1553073 Krt17 keratin 17 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1553073 Krt17 keratin 17 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12050118 1553073 Krt17 keratin 17 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12050118 1553073 Krt17 keratin 17 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:12050118 1553073 Krt17 keratin 17 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:15601842 1553073 Krt17 keratin 17 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15601842 1553073 Krt17 keratin 17 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:12050118 1553073 Krt17 keratin 17 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1553073 Krt17 keratin 17 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1553073 Krt17 keratin 17 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20230504 MGI PMID:33008845 1553073 Krt17 keratin 17 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:12050118 1553073 Krt17 keratin 17 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:15601842 1553073 Krt17 keratin 17 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:12050118 1553073 Krt17 keratin 17 gene MP:0003812 abnormal hair medulla IAGP N RGD:5509061 20141003 MGI PMID:12050118 1553073 Krt17 keratin 17 gene MP:0003848 brittle hair IAGP N RGD:5509061 20141003 MGI PMID:12050118 1553073 Krt17 keratin 17 gene MP:0005072 abnormal hair follicle melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:12050118 1553073 Krt17 keratin 17 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20201022 MGI 1553073 Krt17 keratin 17 gene MP:0010686 abnormal hair follicle matrix region morphology IAGP N RGD:5509061 20141003 MGI PMID:12050118 1553073 Krt17 keratin 17 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15601842 1553073 Krt17 keratin 17 gene MP:0011195 increased hair follicle apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12050118 1553074 Chpt1 choline phosphotransferase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1553075 Nudt5 nudix hydrolase 5 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1553075 Nudt5 nudix hydrolase 5 gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20220811 MGI 1553075 Nudt5 nudix hydrolase 5 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1553077 Ncl nucleolin gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20220113 MGI PMID:34515347 1553077 Ncl nucleolin gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20220113 MGI PMID:34515347 1553078 Chmp3 charged multivesicular body protein 3 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201231 MGI 1553078 Chmp3 charged multivesicular body protein 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1553078 Chmp3 charged multivesicular body protein 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553078 Chmp3 charged multivesicular body protein 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1553079 Crcp calcitonin gene-related peptide-receptor component protein gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20240523 MGI 1553079 Crcp calcitonin gene-related peptide-receptor component protein gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1553079 Crcp calcitonin gene-related peptide-receptor component protein gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1553079 Crcp calcitonin gene-related peptide-receptor component protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553079 Crcp calcitonin gene-related peptide-receptor component protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1553080 Dctn2 dynactin 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553081 Samd7 sterile alpha motif domain containing 7 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200310 MGI PMID:28900001 1553081 Samd7 sterile alpha motif domain containing 7 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201022 MGI 1553081 Samd7 sterile alpha motif domain containing 7 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20230907 MGI PMID:33603070 1553081 Samd7 sterile alpha motif domain containing 7 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20230907 MGI PMID:33603070 1553081 Samd7 sterile alpha motif domain containing 7 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20230907 MGI PMID:33603070 1553081 Samd7 sterile alpha motif domain containing 7 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20200310 MGI PMID:28900001 1553081 Samd7 sterile alpha motif domain containing 7 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20230907 MGI PMID:33603070 1553081 Samd7 sterile alpha motif domain containing 7 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20230907 MGI PMID:33603070 1553081 Samd7 sterile alpha motif domain containing 7 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20230907 MGI PMID:33603070 1553081 Samd7 sterile alpha motif domain containing 7 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200310 MGI PMID:28900001 1553081 Samd7 sterile alpha motif domain containing 7 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20230907 MGI PMID:33603070 1553081 Samd7 sterile alpha motif domain containing 7 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200310 MGI PMID:28900001 1553081 Samd7 sterile alpha motif domain containing 7 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20230907 MGI PMID:33603070 1553081 Samd7 sterile alpha motif domain containing 7 gene MP:0012150 increased b-wave implicit time IAGP N RGD:5509061 20230907 MGI PMID:33603070 1553084 Sipa1 signal-induced proliferation associated gene 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12892713 1553084 Sipa1 signal-induced proliferation associated gene 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12892713 1553084 Sipa1 signal-induced proliferation associated gene 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:12892713 1553084 Sipa1 signal-induced proliferation associated gene 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:12892713 1553084 Sipa1 signal-induced proliferation associated gene 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12892713 1553084 Sipa1 signal-induced proliferation associated gene 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12892713 1553084 Sipa1 signal-induced proliferation associated gene 1 gene MP:0001410 head bobbing IEA N RGD:5509061 20200514 MGI 1553084 Sipa1 signal-induced proliferation associated gene 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12892713 1553084 Sipa1 signal-induced proliferation associated gene 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12892713 1553084 Sipa1 signal-induced proliferation associated gene 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12892713 1553084 Sipa1 signal-induced proliferation associated gene 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12892713 1553084 Sipa1 signal-induced proliferation associated gene 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:12892713 1553084 Sipa1 signal-induced proliferation associated gene 1 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:12892713 1553084 Sipa1 signal-induced proliferation associated gene 1 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:12892713 1553085 Serinc1 serine incorporator 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20141003 MGI 1553085 Serinc1 serine incorporator 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1553085 Serinc1 serine incorporator 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20141003 MGI 1553087 Gdpd3 glycerophosphodiester phosphodiesterase domain containing 3 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210722 MGI PMID:30224518 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0000414 alopecia IAGP N RGD:5509061 20200310 MGI PMID:15491998 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0000414 alopecia IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001190 reddish skin IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20200310 MGI PMID:15491998 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001192 scaly skin IAGP N RGD:5509061 20200310 MGI PMID:15491998 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001194 dermatitis IAGP N RGD:5509061 20200310 MGI PMID:15241416 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001194 dermatitis IAGP N RGD:5509061 20200310 MGI PMID:15491998 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001194 dermatitis IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001194 dermatitis IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001200 thick skin IAGP N RGD:5509061 20200310 MGI PMID:15491998 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20200310 MGI PMID:15491998 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001212 skin lesions IAGP N RGD:5509061 20200310 MGI PMID:15671285 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20200310 MGI PMID:15491998 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001412 excessive scratching IAGP N RGD:5509061 20200310 MGI PMID:15491998 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001786 skin edema IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001851 eye inflammation IAGP N RGD:5509061 20200310 MGI PMID:15671285 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001851 eye inflammation IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20200310 MGI PMID:15671285 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001874 acanthosis IAGP N RGD:5509061 20200310 MGI PMID:15491998 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0001874 acanthosis IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20200310 MGI PMID:15491998 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0002433 abnormal T-helper 1 cell morphology IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:15241416 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0002497 increased IgE level IAGP N RGD:5509061 20200310 MGI PMID:15491998 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0002497 increased IgE level IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200310 MGI PMID:15241416 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0003427 parakeratosis IAGP N RGD:5509061 20200310 MGI PMID:15491998 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0004481 abnormal conjunctival epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0004947 skin inflammation IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0005251 blepharitis IAGP N RGD:5509061 20200310 MGI PMID:15671285 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0005251 blepharitis IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0006167 eyelid edema IAGP N RGD:5509061 20200310 MGI PMID:15491998 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0006167 eyelid edema IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0008556 abnormal tumor necrosis factor secretion IAGP N RGD:5509061 20200310 MGI PMID:15241416 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20200310 MGI PMID:15241416 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20200310 MGI PMID:15241416 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15491998 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0012164 abnormal conjunctiva goblet cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15241416 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0013452 increased lacrimal gland apoptosis IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0013459 perioral dermatitis IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0013460 periocular dermatitis IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0013464 decreased conjunctiva goblet cell number IAGP N RGD:5509061 20200310 MGI PMID:15671285 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0013464 decreased conjunctiva goblet cell number IAGP N RGD:5509061 20200310 MGI PMID:18441309 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0013478 corneal limbitis IAGP N RGD:5509061 20200310 MGI PMID:15671285 1553089 Nfkbiz nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, zeta gene MP:0020220 decreased tear production IAGP N RGD:5509061 20200310 MGI PMID:23453632 1553090 Rab8b RAB8B, member RAS oncogene family gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24213529 1553090 Rab8b RAB8B, member RAS oncogene family gene MP:0008109 abnormal small intestinal microvillus morphology IAGP N RGD:5509061 20141003 MGI PMID:24213529 1553090 Rab8b RAB8B, member RAS oncogene family gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24213529 1553094 Klk12 kallikrein related-peptidase 12 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1553094 Klk12 kallikrein related-peptidase 12 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20201231 MGI 1553096 Zfand6 zinc finger, AN1-type domain 6 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1553096 Zfand6 zinc finger, AN1-type domain 6 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1553096 Zfand6 zinc finger, AN1-type domain 6 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1553096 Zfand6 zinc finger, AN1-type domain 6 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1553096 Zfand6 zinc finger, AN1-type domain 6 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20201022 MGI 1553096 Zfand6 zinc finger, AN1-type domain 6 gene MP:0001147 small testis IEA N RGD:5509061 20201022 MGI 1553096 Zfand6 zinc finger, AN1-type domain 6 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1553096 Zfand6 zinc finger, AN1-type domain 6 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1553096 Zfand6 zinc finger, AN1-type domain 6 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 1553096 Zfand6 zinc finger, AN1-type domain 6 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20201022 MGI 1553096 Zfand6 zinc finger, AN1-type domain 6 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200514 MGI 1553096 Zfand6 zinc finger, AN1-type domain 6 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1553096 Zfand6 zinc finger, AN1-type domain 6 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20200514 MGI 1553096 Zfand6 zinc finger, AN1-type domain 6 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20221215 MGI 1553097 Fbxo45 F-box protein 45 gene MP:0000160 kyphosis IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0001512 trunk curl IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0003717 pallor IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0008129 absent brain internal capsule IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0008503 abnormal spinal cord grey matter morphology IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553097 Fbxo45 F-box protein 45 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19398581 1553098 Atrx ATRX, chromatin remodeler gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20111116 MGI 1553098 Atrx ATRX, chromatin remodeler gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16628246 1553098 Atrx ATRX, chromatin remodeler gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:15668733 1553098 Atrx ATRX, chromatin remodeler gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20865721 1553098 Atrx ATRX, chromatin remodeler gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:19088125 1553098 Atrx ATRX, chromatin remodeler gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:15668733 1553098 Atrx ATRX, chromatin remodeler gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:20865721 1553098 Atrx ATRX, chromatin remodeler gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16628246 1553098 Atrx ATRX, chromatin remodeler gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:16628246 1553098 Atrx ATRX, chromatin remodeler gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:16628246 1553098 Atrx ATRX, chromatin remodeler gene MP:0002084 abnormal developmental patterning IEA N RGD:5509061 20111116 MGI 1553098 Atrx ATRX, chromatin remodeler gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:16628246 1553098 Atrx ATRX, chromatin remodeler gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:16628246 1553098 Atrx ATRX, chromatin remodeler gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:15668733 1553098 Atrx ATRX, chromatin remodeler gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:15668733 1553098 Atrx ATRX, chromatin remodeler gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19088125 1553098 Atrx ATRX, chromatin remodeler gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:16628246 1553098 Atrx ATRX, chromatin remodeler gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:36073547 1553098 Atrx ATRX, chromatin remodeler gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16628246 1553098 Atrx ATRX, chromatin remodeler gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:16628246 1553098 Atrx ATRX, chromatin remodeler gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16628246 1553098 Atrx ATRX, chromatin remodeler gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:16628246 1553098 Atrx ATRX, chromatin remodeler gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19088125 1553098 Atrx ATRX, chromatin remodeler gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19088125 1553098 Atrx ATRX, chromatin remodeler gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19088125 1553098 Atrx ATRX, chromatin remodeler gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:19088125 1553098 Atrx ATRX, chromatin remodeler gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:20865721 1553098 Atrx ATRX, chromatin remodeler gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:15668733 1553098 Atrx ATRX, chromatin remodeler gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15668733 1553098 Atrx ATRX, chromatin remodeler gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:15668733 1553098 Atrx ATRX, chromatin remodeler gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20230601 MGI PMID:36073547 1553098 Atrx ATRX, chromatin remodeler gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15668733 1553098 Atrx ATRX, chromatin remodeler gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15668733 1553098 Atrx ATRX, chromatin remodeler gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16628246 1553098 Atrx ATRX, chromatin remodeler gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20865721 1553098 Atrx ATRX, chromatin remodeler gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16628246 1553101 Gprasp1 G protein-coupled receptor associated sorting protein 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:19712096 1553101 Gprasp1 G protein-coupled receptor associated sorting protein 1 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:19712096 1553101 Gprasp1 G protein-coupled receptor associated sorting protein 1 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:20543951 1553104 Yipf1 Yip1 domain family, member 1 gene MP:0001391 abnormal tail movements IEA N RGD:5509061 20200310 MGI 1553104 Yipf1 Yip1 domain family, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:24652767 1553107 Nox3 NADPH oxidase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12434016 1553107 Nox3 NADPH oxidase 3 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1553107 Nox3 NADPH oxidase 3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:9755211 1553107 Nox3 NADPH oxidase 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20111116 MGI 1553107 Nox3 NADPH oxidase 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15014044 1553107 Nox3 NADPH oxidase 3 gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 1553107 Nox3 NADPH oxidase 3 gene MP:0001443 poor grooming IEA N RGD:5509061 20111116 MGI 1553107 Nox3 NADPH oxidase 3 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:12434016 1553107 Nox3 NADPH oxidase 3 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:15014044 1553107 Nox3 NADPH oxidase 3 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:9755211 1553107 Nox3 NADPH oxidase 3 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:15014044 1553107 Nox3 NADPH oxidase 3 gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20141003 MGI PMID:10491954 1553107 Nox3 NADPH oxidase 3 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:10491954 1553107 Nox3 NADPH oxidase 3 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:15014044 1553107 Nox3 NADPH oxidase 3 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:21161235 1553107 Nox3 NADPH oxidase 3 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:9755211 1553107 Nox3 NADPH oxidase 3 gene MP:0002980 abnormal postural reflex IAGP N RGD:5509061 20141003 MGI PMID:15014044 1553107 Nox3 NADPH oxidase 3 gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:10491954 1553107 Nox3 NADPH oxidase 3 gene MP:0004845 absent vestibuloocular reflex IAGP N RGD:5509061 20141003 MGI PMID:12711080 1553107 Nox3 NADPH oxidase 3 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:10491954 1553107 Nox3 NADPH oxidase 3 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:10835400 1553107 Nox3 NADPH oxidase 3 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:15014044 1553107 Nox3 NADPH oxidase 3 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:21161235 1553107 Nox3 NADPH oxidase 3 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:9755211 1553107 Nox3 NADPH oxidase 3 gene MP:0005424 jerky movement IEA N RGD:5509061 20111116 MGI 1553107 Nox3 NADPH oxidase 3 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:12434016 1553107 Nox3 NADPH oxidase 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12434016 1553107 Nox3 NADPH oxidase 3 gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20171012 MGI PMID:12434016 1553107 Nox3 NADPH oxidase 3 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:12434016 1553108 Ldhal6b lactate dehydrogenase A-like 6B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210826 MGI 1553109 Ehd3 EH-domain containing 3 gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0011369 increased renal glomerulus apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0011455 absent glomerular endothelium fenestra IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553109 Ehd3 EH-domain containing 3 gene MP:0011512 mesangial cell interposition IAGP N RGD:5509061 20141003 MGI PMID:21408024 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20200310 MGI PMID:18353305 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200310 MGI 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0001125 abnormal oocyte morphology IEA N RGD:5509061 20111116 MGI 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0001147 small testis IEA N RGD:5509061 20200310 MGI 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220519 MGI 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20200310 MGI PMID:18353305 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:18353305 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:18353305 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0001932 abnormal spermiogenesis IEA N RGD:5509061 20111116 MGI 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20200310 MGI 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20200310 MGI 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20200310 MGI PMID:18353305 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:18353305 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20200310 MGI PMID:18353305 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0002687 oligozoospermia IEA N RGD:5509061 20111116 MGI 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200310 MGI PMID:18353305 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20200310 MGI PMID:18353305 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220519 MGI 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20200310 MGI PMID:18353305 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18353305 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20200310 MGI PMID:18353305 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20200310 MGI PMID:18353305 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0009325 necrospermia IAGP N RGD:5509061 20200310 MGI PMID:18353305 1553111 Brwd1 bromodomain and WD repeat domain containing 1 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20200310 MGI PMID:18353305 1553115 Ifnk interferon kappa gene MP:0000452 abnormal mouth morphology IEA N RGD:5509061 20181227 MGI 1553115 Ifnk interferon kappa gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20220407 MGI PMID:34364883 1553115 Ifnk interferon kappa gene MP:0012573 decreased susceptibility to chemically induced skin inflammation IAGP N RGD:5509061 20220407 MGI PMID:34364883 1553116 Lrrc41 leucine rich repeat containing 41 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20220811 MGI 1553116 Lrrc41 leucine rich repeat containing 41 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1553116 Lrrc41 leucine rich repeat containing 41 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 1553116 Lrrc41 leucine rich repeat containing 41 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20201022 MGI 1553116 Lrrc41 leucine rich repeat containing 41 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1553116 Lrrc41 leucine rich repeat containing 41 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20210128 MGI 1553116 Lrrc41 leucine rich repeat containing 41 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1553116 Lrrc41 leucine rich repeat containing 41 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1553116 Lrrc41 leucine rich repeat containing 41 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20220811 MGI 1553117 Krt5 keratin 5 gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11408584 1553117 Krt5 keratin 5 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:11408584 1553117 Krt5 keratin 5 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:11408584 1553117 Krt5 keratin 5 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11408584 1553117 Krt5 keratin 5 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11408584 1553117 Krt5 keratin 5 gene MP:0001258 decreased body length IEA N RGD:5509061 20221215 MGI 1553117 Krt5 keratin 5 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:11408584 1553117 Krt5 keratin 5 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1553117 Krt5 keratin 5 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:11408584 1553117 Krt5 keratin 5 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:11408584 1553117 Krt5 keratin 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11408584 1553117 Krt5 keratin 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1553117 Krt5 keratin 5 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1553119 Slc9c1 solute carrier family 9, subfamily C (Na+-transporting carboxylic acid decarboxylase), member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:14634667 1553119 Slc9c1 solute carrier family 9, subfamily C (Na+-transporting carboxylic acid decarboxylase), member 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:14634667 1553120 Pmch pro-melanin-concentrating hormone gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1553120 Pmch pro-melanin-concentrating hormone gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1553120 Pmch pro-melanin-concentrating hormone gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12897241 1553120 Pmch pro-melanin-concentrating hormone gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22232663 1553120 Pmch pro-melanin-concentrating hormone gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9872314 1553120 Pmch pro-melanin-concentrating hormone gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12897241 1553120 Pmch pro-melanin-concentrating hormone gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:22232663 1553120 Pmch pro-melanin-concentrating hormone gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:22232663 1553120 Pmch pro-melanin-concentrating hormone gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:22232663 1553120 Pmch pro-melanin-concentrating hormone gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12897241 1553120 Pmch pro-melanin-concentrating hormone gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12897241 1553120 Pmch pro-melanin-concentrating hormone gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1553120 Pmch pro-melanin-concentrating hormone gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12897241 1553120 Pmch pro-melanin-concentrating hormone gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:12897241 1553120 Pmch pro-melanin-concentrating hormone gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:9872314 1553120 Pmch pro-melanin-concentrating hormone gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12897241 1553120 Pmch pro-melanin-concentrating hormone gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22232663 1553120 Pmch pro-melanin-concentrating hormone gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9872314 1553120 Pmch pro-melanin-concentrating hormone gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:12897241 1553120 Pmch pro-melanin-concentrating hormone gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12897241 1553120 Pmch pro-melanin-concentrating hormone gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12897241 1553120 Pmch pro-melanin-concentrating hormone gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:9872314 1553120 Pmch pro-melanin-concentrating hormone gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22232663 1553120 Pmch pro-melanin-concentrating hormone gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1553120 Pmch pro-melanin-concentrating hormone gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:9872314 1553120 Pmch pro-melanin-concentrating hormone gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:12897241 1553120 Pmch pro-melanin-concentrating hormone gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:12897241 1553120 Pmch pro-melanin-concentrating hormone gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:9872314 1553121 Frmd4a FERM domain containing 4A gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20230601 MGI 1553121 Frmd4a FERM domain containing 4A gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220519 MGI 1553121 Frmd4a FERM domain containing 4A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1553125 Toe1 target of EGR1, member 1 (nuclear) gene MP:0001513 limb grasping IEA N RGD:5509061 20201231 MGI 1553125 Toe1 target of EGR1, member 1 (nuclear) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20191114 MGI PMID:28092684 1553125 Toe1 target of EGR1, member 1 (nuclear) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553125 Toe1 target of EGR1, member 1 (nuclear) gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20211021 MGI 1553125 Toe1 target of EGR1, member 1 (nuclear) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1553126 Nifk nucleolar protein interacting with the FHA domain of MKI67 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1553126 Nifk nucleolar protein interacting with the FHA domain of MKI67 gene MP:0001293 anophthalmia IEA N RGD:5509061 20220811 MGI 1553126 Nifk nucleolar protein interacting with the FHA domain of MKI67 gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 1553126 Nifk nucleolar protein interacting with the FHA domain of MKI67 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1553126 Nifk nucleolar protein interacting with the FHA domain of MKI67 gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20241003 MGI 1553126 Nifk nucleolar protein interacting with the FHA domain of MKI67 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220811 MGI 1553126 Nifk nucleolar protein interacting with the FHA domain of MKI67 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1553126 Nifk nucleolar protein interacting with the FHA domain of MKI67 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1553126 Nifk nucleolar protein interacting with the FHA domain of MKI67 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241003 MGI 1553126 Nifk nucleolar protein interacting with the FHA domain of MKI67 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241003 MGI 1553126 Nifk nucleolar protein interacting with the FHA domain of MKI67 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1553126 Nifk nucleolar protein interacting with the FHA domain of MKI67 gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20241003 MGI 1553126 Nifk nucleolar protein interacting with the FHA domain of MKI67 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24469832 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24469832 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:24469832 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:24469832 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20211104 MGI PMID:26240281 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20150702 MGI PMID:24469832 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24469832 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:24469832 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20211104 MGI PMID:26240281 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:24469832 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0004264 abnormal extraembryonic tissue physiology IAGP N RGD:5509061 20211104 MGI PMID:26240281 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:24469832 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:24469832 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:24469832 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:24469832 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:24469832 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20211104 MGI PMID:26240281 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20211104 MGI PMID:26240281 1553129 Fbxw11 F-box and WD-40 domain protein 11 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:24469832 1553130 Atf5 activating transcription factor 5 gene MP:0001003 abnormal olfactory receptor morphology IAGP N RGD:5509061 20141003 MGI PMID:24120133 1553130 Atf5 activating transcription factor 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23090999 1553130 Atf5 activating transcription factor 5 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23090999 1553130 Atf5 activating transcription factor 5 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:24120133 1553130 Atf5 activating transcription factor 5 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:24120133 1553130 Atf5 activating transcription factor 5 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23090999 1553130 Atf5 activating transcription factor 5 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:23090999 1553130 Atf5 activating transcription factor 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23090999 1553130 Atf5 activating transcription factor 5 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23090999 1553131 Hyal4 hyaluronoglucosaminidase 4 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1553131 Hyal4 hyaluronoglucosaminidase 4 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20220811 MGI 1553135 Slc12a8 solute carrier family 12 (potassium/chloride transporters), member 8 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1553135 Slc12a8 solute carrier family 12 (potassium/chloride transporters), member 8 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20191128 MGI PMID:31131364 1553135 Slc12a8 solute carrier family 12 (potassium/chloride transporters), member 8 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20191128 MGI PMID:31131364 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0000256 echinocytosis IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0010035 increased erythrocyte clearance IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553136 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 gene MP:0010177 acanthocytosis IAGP N RGD:5509061 20200310 MGI PMID:24739386 1553140 Taar1 trace amine-associated receptor 1 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20200310 MGI PMID:17212650 1553140 Taar1 trace amine-associated receptor 1 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20200310 MGI PMID:22114263 1553140 Taar1 trace amine-associated receptor 1 gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20200310 MGI PMID:17212650 1553140 Taar1 trace amine-associated receptor 1 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20200310 MGI PMID:17212650 1553140 Taar1 trace amine-associated receptor 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:25740289 1553140 Taar1 trace amine-associated receptor 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:17212650 1553140 Taar1 trace amine-associated receptor 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:22114263 1553140 Taar1 trace amine-associated receptor 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:22114263 1553140 Taar1 trace amine-associated receptor 1 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:22114263 1553140 Taar1 trace amine-associated receptor 1 gene MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20200310 MGI PMID:17212650 1553140 Taar1 trace amine-associated receptor 1 gene MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20200310 MGI PMID:25740289 1553140 Taar1 trace amine-associated receptor 1 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20200310 MGI PMID:22114263 1553140 Taar1 trace amine-associated receptor 1 gene MP:0011016 increased core body temperature IAGP N RGD:5509061 20200310 MGI PMID:22114263 1553140 Taar1 trace amine-associated receptor 1 gene MP:0012342 high preference for an addictive substance IAGP N RGD:5509061 20220317 MGI PMID:34512422 1553140 Taar1 trace amine-associated receptor 1 gene MP:0012733 abnormal behavioral response to methamphetamine IAGP N RGD:5509061 20220317 MGI PMID:34512422 1553142 Fam13b family with sequence similarity 13, member B gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1553142 Fam13b family with sequence similarity 13, member B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1553143 Pnpla5 patatin-like phospholipase domain containing 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1553143 Pnpla5 patatin-like phospholipase domain containing 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1553146 Wdr77 WD repeat domain 77 gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:17032745 1553146 Wdr77 WD repeat domain 77 gene MP:0000666 decreased prostate gland duct number IAGP N RGD:5509061 20200310 MGI PMID:20519372 1553146 Wdr77 WD repeat domain 77 gene MP:0001163 abnormal prostate gland anterior lobe morphology IAGP N RGD:5509061 20200310 MGI PMID:20519372 1553146 Wdr77 WD repeat domain 77 gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:17032745 1553146 Wdr77 WD repeat domain 77 gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:20519372 1553146 Wdr77 WD repeat domain 77 gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:17032745 1553146 Wdr77 WD repeat domain 77 gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:20519372 1553146 Wdr77 WD repeat domain 77 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:20519372 1553146 Wdr77 WD repeat domain 77 gene MP:0002774 small prostate gland IAGP N RGD:5509061 20200310 MGI PMID:20519372 1553146 Wdr77 WD repeat domain 77 gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20200310 MGI PMID:20519372 1553146 Wdr77 WD repeat domain 77 gene MP:0009380 abnormal prostate gland ventral lobe morphology IAGP N RGD:5509061 20200310 MGI PMID:20519372 1553146 Wdr77 WD repeat domain 77 gene MP:0009381 abnormal prostate gland dorsolateral lobe morphology IAGP N RGD:5509061 20200310 MGI PMID:20519372 1553146 Wdr77 WD repeat domain 77 gene MP:0009734 abnormal prostate gland duct morphology IAGP N RGD:5509061 20200310 MGI PMID:20519372 1553146 Wdr77 WD repeat domain 77 gene MP:0009735 abnormal prostate gland development IAGP N RGD:5509061 20200310 MGI PMID:20519372 1553146 Wdr77 WD repeat domain 77 gene MP:0009736 abnormal prostate gland branching morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:20519372 1553146 Wdr77 WD repeat domain 77 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17032745 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:8064243 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:9647223 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0002144 abnormal B cell differentiation IEA N RGD:5509061 20200310 MGI 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0002493 increased IgG level IEA N RGD:5509061 20200310 MGI 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20200310 MGI PMID:8064243 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20200310 MGI PMID:9647223 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20200310 MGI PMID:7889415 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20200310 MGI PMID:7889415 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:8064243 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:9647223 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:7889415 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:7889415 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200310 MGI PMID:9647223 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:7889415 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:17082573 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:17082573 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:7889415 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:8064243 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:9647223 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:8064243 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20200310 MGI PMID:7889415 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1553149 Cd8b1 CD8 subunit beta 1 gene MP:0020155 enhanced humoral immune response IEA N RGD:5509061 20200310 MGI 1553151 Or2y1g olfactory receptor family 2 subfamily Y member 1G gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20190905 MGI PMID:27739476 1553151 Or2y1g olfactory receptor family 2 subfamily Y member 1G gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20190905 MGI PMID:27739476 1553154 Gpaa1 GPI anchor attachment protein 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1553154 Gpaa1 GPI anchor attachment protein 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 1553154 Gpaa1 GPI anchor attachment protein 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1553154 Gpaa1 GPI anchor attachment protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553154 Gpaa1 GPI anchor attachment protein 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1553155 Foxo3 forkhead box O3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200310 MGI 1553155 Foxo3 forkhead box O3 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:15308101 1553155 Foxo3 forkhead box O3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:15308101 1553155 Foxo3 forkhead box O3 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:15308101 1553155 Foxo3 forkhead box O3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:15308101 1553155 Foxo3 forkhead box O3 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:12855809 1553155 Foxo3 forkhead box O3 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20200310 MGI PMID:14978268 1553155 Foxo3 forkhead box O3 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20200310 MGI PMID:12855809 1553155 Foxo3 forkhead box O3 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20200310 MGI PMID:15308101 1553155 Foxo3 forkhead box O3 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:26061565 1553155 Foxo3 forkhead box O3 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0001194 dermatitis IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1553155 Foxo3 forkhead box O3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20200310 MGI 1553155 Foxo3 forkhead box O3 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20200310 MGI 1553155 Foxo3 forkhead box O3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20200310 MGI PMID:25264246 1553155 Foxo3 forkhead box O3 gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:12855809 1553155 Foxo3 forkhead box O3 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0001749 suppressed circulating follicle stimulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:26061565 1553155 Foxo3 forkhead box O3 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:12855809 1553155 Foxo3 forkhead box O3 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20200310 MGI PMID:12855809 1553155 Foxo3 forkhead box O3 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20200310 MGI PMID:15308101 1553155 Foxo3 forkhead box O3 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:15308101 1553155 Foxo3 forkhead box O3 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20200310 MGI PMID:15308101 1553155 Foxo3 forkhead box O3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:15308101 1553155 Foxo3 forkhead box O3 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20200310 MGI PMID:15308101 1553155 Foxo3 forkhead box O3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:12855809 1553155 Foxo3 forkhead box O3 gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:18371339 1553155 Foxo3 forkhead box O3 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20200310 MGI PMID:12855809 1553155 Foxo3 forkhead box O3 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20200310 MGI PMID:26061565 1553155 Foxo3 forkhead box O3 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0002047 increased hepatic hemangioma incidence IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200310 MGI PMID:25264246 1553155 Foxo3 forkhead box O3 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:15308101 1553155 Foxo3 forkhead box O3 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20200310 MGI PMID:18371339 1553155 Foxo3 forkhead box O3 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20200310 MGI PMID:12855809 1553155 Foxo3 forkhead box O3 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20200310 MGI PMID:18371339 1553155 Foxo3 forkhead box O3 gene MP:0002681 increased corpora lutea number IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20200310 MGI PMID:14978268 1553155 Foxo3 forkhead box O3 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20200310 MGI PMID:15308101 1553155 Foxo3 forkhead box O3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:25264246 1553155 Foxo3 forkhead box O3 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20200310 MGI PMID:26061565 1553155 Foxo3 forkhead box O3 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1553155 Foxo3 forkhead box O3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:18371339 1553155 Foxo3 forkhead box O3 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20211021 MGI 1553155 Foxo3 forkhead box O3 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:25264246 1553155 Foxo3 forkhead box O3 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210520 MGI 1553155 Foxo3 forkhead box O3 gene MP:0003505 increased prolactinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20200310 MGI PMID:18601916 1553155 Foxo3 forkhead box O3 gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20200310 MGI PMID:25264246 1553155 Foxo3 forkhead box O3 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18371339 1553155 Foxo3 forkhead box O3 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20200310 MGI PMID:18371339 1553155 Foxo3 forkhead box O3 gene MP:0004832 enlarged ovary IAGP N RGD:5509061 20200310 MGI PMID:12855809 1553155 Foxo3 forkhead box O3 gene MP:0004832 enlarged ovary IAGP N RGD:5509061 20200310 MGI PMID:18601916 1553155 Foxo3 forkhead box O3 gene MP:0004832 enlarged ovary IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0005068 abnormal NK cell morphology IAGP N RGD:5509061 20200310 MGI PMID:17618288 1553155 Foxo3 forkhead box O3 gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20200310 MGI PMID:26061565 1553155 Foxo3 forkhead box O3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:12855809 1553155 Foxo3 forkhead box O3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:25264246 1553155 Foxo3 forkhead box O3 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:15308101 1553155 Foxo3 forkhead box O3 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:26061565 1553155 Foxo3 forkhead box O3 gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20200310 MGI PMID:18371339 1553155 Foxo3 forkhead box O3 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20200310 MGI PMID:25264246 1553155 Foxo3 forkhead box O3 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:17618288 1553155 Foxo3 forkhead box O3 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20200310 MGI PMID:17618288 1553155 Foxo3 forkhead box O3 gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20220331 MGI PMID:26061565 1553155 Foxo3 forkhead box O3 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:17618288 1553155 Foxo3 forkhead box O3 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20200310 MGI PMID:12855809 1553155 Foxo3 forkhead box O3 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20200310 MGI PMID:14978268 1553155 Foxo3 forkhead box O3 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20200310 MGI PMID:15308101 1553155 Foxo3 forkhead box O3 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20200310 MGI PMID:12855809 1553155 Foxo3 forkhead box O3 gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20200310 MGI PMID:14978268 1553155 Foxo3 forkhead box O3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1553155 Foxo3 forkhead box O3 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:25264246 1553155 Foxo3 forkhead box O3 gene MP:0009361 abnormal primordial ovarian follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:18601916 1553155 Foxo3 forkhead box O3 gene MP:0009361 abnormal primordial ovarian follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0009442 increased ovarian teratoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0009442 increased ovarian teratoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0009648 abnormal superovulation IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:18371339 1553155 Foxo3 forkhead box O3 gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20220519 MGI 1553155 Foxo3 forkhead box O3 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20200310 MGI 1553155 Foxo3 forkhead box O3 gene MP:0012121 sclerocornea IEA N RGD:5509061 20200310 MGI 1553155 Foxo3 forkhead box O3 gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:26061565 1553155 Foxo3 forkhead box O3 gene MP:0012437 increased Harderian gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:17254969 1553155 Foxo3 forkhead box O3 gene MP:0012736 abnormal polar body morphology IAGP N RGD:5509061 20200310 MGI PMID:21347845 1553155 Foxo3 forkhead box O3 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:12855809 1553155 Foxo3 forkhead box O3 gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:21347845 1553159 Yipf5 Yip1 domain family, member 5 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1553159 Yipf5 Yip1 domain family, member 5 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20211021 MGI 1553159 Yipf5 Yip1 domain family, member 5 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20201231 MGI 1553159 Yipf5 Yip1 domain family, member 5 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20200310 MGI 1553159 Yipf5 Yip1 domain family, member 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553159 Yipf5 Yip1 domain family, member 5 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 1553159 Yipf5 Yip1 domain family, member 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1553159 Yipf5 Yip1 domain family, member 5 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1553164 Cenpc1 centromere protein C1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9448298 1553164 Cenpc1 centromere protein C1 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:9448298 1553164 Cenpc1 centromere protein C1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9448298 1553164 Cenpc1 centromere protein C1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:9448298 1553164 Cenpc1 centromere protein C1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9448298 1553165 Mlh3 mutL homolog 3 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12091911 1553165 Mlh3 mutL homolog 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12091911 1553165 Mlh3 mutL homolog 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12091911 1553165 Mlh3 mutL homolog 3 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:12091911 1553165 Mlh3 mutL homolog 3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:12091911 1553165 Mlh3 mutL homolog 3 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:12091911 1553165 Mlh3 mutL homolog 3 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12091911 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:19114101 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:19114101 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20190530 MGI PMID:26306834 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0000913 abnormal brain development IEA N RGD:5509061 20170330 MGI 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19114101 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0001326 retina degeneration IEA N RGD:5509061 20170330 MGI 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20190530 MGI PMID:26306834 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19114101 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0003044 impaired basement membrane formation IAGP N RGD:5509061 20141003 MGI PMID:23454088 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:23454088 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170330 MGI 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:19017726 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:19114101 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0005623 abnormal meninges morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0008030 abnormal Cajal-Retzius cell morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0009026 abnormal brain pia mater morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:19114101 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:16458488 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:19114101 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0009410 abnormal skeletal muscle satellite cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19114101 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0009959 abnormal cerebellar hemisphere morphology IAGP N RGD:5509061 20190530 MGI PMID:26306834 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0010098 abnormal retina blood vessel pattern IEA N RGD:5509061 20170330 MGI 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0010235 abnormal retina inner limiting membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:23454088 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0010452 retina microaneurysm IEA N RGD:5509061 20170330 MGI 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19114101 1553166 Pomgnt1 protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20150226 MGI PMID:23118208 1553168 Slc27a1 solute carrier family 27 (fatty acid transporter), member 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:14991074 1553168 Slc27a1 solute carrier family 27 (fatty acid transporter), member 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14991074 1553168 Slc27a1 solute carrier family 27 (fatty acid transporter), member 1 gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:14991074 1553168 Slc27a1 solute carrier family 27 (fatty acid transporter), member 1 gene MP:0031413 abnormal skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:14991074 1553168 Slc27a1 solute carrier family 27 (fatty acid transporter), member 1 gene MP:0031617 abnormal skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:14991074 1553171 Gpr153 G protein-coupled receptor 153 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1553171 Gpr153 G protein-coupled receptor 153 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20220519 MGI 1553171 Gpr153 G protein-coupled receptor 153 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1553173 Tspan2 tetraspanin 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20200310 MGI PMID:24038504 1553173 Tspan2 tetraspanin 2 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20200310 MGI PMID:24038504 1553173 Tspan2 tetraspanin 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20200310 MGI PMID:24038504 1553173 Tspan2 tetraspanin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:24038504 1553173 Tspan2 tetraspanin 2 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20200310 MGI PMID:24038504 1553173 Tspan2 tetraspanin 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200310 MGI PMID:24038504 1553173 Tspan2 tetraspanin 2 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20200310 MGI PMID:24038504 1553173 Tspan2 tetraspanin 2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20200310 MGI PMID:24038504 1553173 Tspan2 tetraspanin 2 gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20200310 MGI PMID:24038504 1553174 Rab1b RAB1B, member RAS oncogene family gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16244655 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1117319 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7416238 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:5709840 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:5709840 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:20643756 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000756 forelimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:1955109 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:4120487 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:1117319 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:5709840 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8027772 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:20643756 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:5709840 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:7349996 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:7416238 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:8027772 1553179 Vps54 VPS54 GARP complex subunit gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:16244655 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:4120487 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16244655 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:1955109 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:5709840 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7416238 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:1955109 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:5709840 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:7416238 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:5709840 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:5709840 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:7416238 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:5709840 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20221215 MGI 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20221215 MGI 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:7416238 1553179 Vps54 VPS54 GARP complex subunit gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:1955109 1553179 Vps54 VPS54 GARP complex subunit gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 1553179 Vps54 VPS54 GARP complex subunit gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:5709840 1553179 Vps54 VPS54 GARP complex subunit gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8006678 1553179 Vps54 VPS54 GARP complex subunit gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:1955109 1553179 Vps54 VPS54 GARP complex subunit gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:20643756 1553179 Vps54 VPS54 GARP complex subunit gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:1383870 1553179 Vps54 VPS54 GARP complex subunit gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:2432278 1553179 Vps54 VPS54 GARP complex subunit gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:8281455 1553179 Vps54 VPS54 GARP complex subunit gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:5709840 1553179 Vps54 VPS54 GARP complex subunit gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:7416238 1553179 Vps54 VPS54 GARP complex subunit gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:4120487 1553179 Vps54 VPS54 GARP complex subunit gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:1955109 1553179 Vps54 VPS54 GARP complex subunit gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:1955109 1553179 Vps54 VPS54 GARP complex subunit gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:1955109 1553179 Vps54 VPS54 GARP complex subunit gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20643756 1553179 Vps54 VPS54 GARP complex subunit gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:5709840 1553179 Vps54 VPS54 GARP complex subunit gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20643756 1553179 Vps54 VPS54 GARP complex subunit gene MP:0003371 decreased circulating estrogen level IAGP N RGD:5509061 20141003 MGI PMID:210748 1553179 Vps54 VPS54 GARP complex subunit gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:3142758 1553179 Vps54 VPS54 GARP complex subunit gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:1117319 1553179 Vps54 VPS54 GARP complex subunit gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:210748 1553179 Vps54 VPS54 GARP complex subunit gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16244655 1553179 Vps54 VPS54 GARP complex subunit gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:20643756 1553179 Vps54 VPS54 GARP complex subunit gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:3947038 1553179 Vps54 VPS54 GARP complex subunit gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:8390608 1553179 Vps54 VPS54 GARP complex subunit gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:1955109 1553179 Vps54 VPS54 GARP complex subunit gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:1117319 1553179 Vps54 VPS54 GARP complex subunit gene MP:0006411 upturned snout IAGP N RGD:5509061 20141003 MGI PMID:7416238 1553179 Vps54 VPS54 GARP complex subunit gene MP:0008460 absent dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:16244655 1553179 Vps54 VPS54 GARP complex subunit gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:20643756 1553179 Vps54 VPS54 GARP complex subunit gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20230615 MGI PMID:1117319 1553179 Vps54 VPS54 GARP complex subunit gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20643756 1553179 Vps54 VPS54 GARP complex subunit gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16244655 1553179 Vps54 VPS54 GARP complex subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16244655 1553179 Vps54 VPS54 GARP complex subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1553179 Vps54 VPS54 GARP complex subunit gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1553179 Vps54 VPS54 GARP complex subunit gene MP:0011987 abnormal GABAergic neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:20643756 1553179 Vps54 VPS54 GARP complex subunit gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:20643756 1553179 Vps54 VPS54 GARP complex subunit gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:20643756 1553179 Vps54 VPS54 GARP complex subunit gene MP:0030140 facial muscle atrophy IAGP N RGD:5509061 20171005 MGI PMID:5709840 1553180 Dele1 DAP3 binding cell death enhancer 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20200514 MGI 1553180 Dele1 DAP3 binding cell death enhancer 1 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20200514 MGI 1553180 Dele1 DAP3 binding cell death enhancer 1 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20201231 MGI 1553180 Dele1 DAP3 binding cell death enhancer 1 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20200514 MGI 1553180 Dele1 DAP3 binding cell death enhancer 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20220811 MGI 1553180 Dele1 DAP3 binding cell death enhancer 1 gene MP:0009453 enhanced contextual conditioning behavior IEA N RGD:5509061 20211021 MGI 1553181 Sgce sarcoglycan, epsilon gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:16099459 1553181 Sgce sarcoglycan, epsilon gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:22040906 1553181 Sgce sarcoglycan, epsilon gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22040906 1553181 Sgce sarcoglycan, epsilon gene MP:0001265 decreased body size IAGP N RGD:5509061 20190815 MGI PMID:27890709 1553181 Sgce sarcoglycan, epsilon gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20190815 MGI PMID:27890709 1553181 Sgce sarcoglycan, epsilon gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201231 MGI 1553181 Sgce sarcoglycan, epsilon gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190815 MGI PMID:27890709 1553181 Sgce sarcoglycan, epsilon gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16099459 1553181 Sgce sarcoglycan, epsilon gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22040906 1553181 Sgce sarcoglycan, epsilon gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190815 MGI PMID:27890709 1553181 Sgce sarcoglycan, epsilon gene MP:0001406 abnormal gait IAGP N RGD:5509061 20190815 MGI PMID:27890709 1553181 Sgce sarcoglycan, epsilon gene MP:0001407 short stride length IAGP N RGD:5509061 20190815 MGI PMID:27890709 1553181 Sgce sarcoglycan, epsilon gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16099459 1553181 Sgce sarcoglycan, epsilon gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:21890494 1553181 Sgce sarcoglycan, epsilon gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:22040906 1553181 Sgce sarcoglycan, epsilon gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:16099459 1553181 Sgce sarcoglycan, epsilon gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21890494 1553181 Sgce sarcoglycan, epsilon gene MP:0003908 decreased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:22040906 1553181 Sgce sarcoglycan, epsilon gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21890494 1553181 Sgce sarcoglycan, epsilon gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20190815 MGI PMID:27890709 1553181 Sgce sarcoglycan, epsilon gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20240523 MGI 1553181 Sgce sarcoglycan, epsilon gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21890494 1553181 Sgce sarcoglycan, epsilon gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:21890494 1553181 Sgce sarcoglycan, epsilon gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:21890494 1553181 Sgce sarcoglycan, epsilon gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20190815 MGI PMID:27890709 1553181 Sgce sarcoglycan, epsilon gene MP:0020422 decreased freezing behavior IEA N RGD:5509061 20240523 MGI 1553182 Casp7 caspase 7 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16469926 1553182 Casp7 caspase 7 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:16469926 1553182 Casp7 caspase 7 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16469926 1553182 Casp7 caspase 7 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:16469926 1553182 Casp7 caspase 7 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16469926 1553182 Casp7 caspase 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16469926 1553182 Casp7 caspase 7 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16469926 1553182 Casp7 caspase 7 gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16469926 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0000141 abnormal vertebral body morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0000297 abnormal atrioventricular cushion morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0000632 abnormal pineal gland morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0000788 abnormal cerebral cortex morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0000963 fused dorsal root ganglion IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0002249 abnormal larynx morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0003105 abnormal heart atrium morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0003130 anal atresia IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0003262 intestinal/bowel diverticulum IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0003617 urinary bladder hypoplasia IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0003922 abnormal heart right atrium morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0004158 right aortic arch IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0004160 retroesophageal right subclavian artery IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0004603 absent vertebral arch IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20181227 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0006065 abnormal heart position or orientation IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0006093 arteriovenous malformation IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0006408 dorsal root ganglion hypoplasia IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0008128 abnormal brain internal capsule morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20181227 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0010200 enlarged lymphatic vessel IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0010490 abnormal inferior vena cava valve morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0010496 abnormal pectinate muscle morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0010595 abnormal aortic valve cusp morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0010602 abnormal pulmonary valve cusp morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0010912 herniated liver IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0011493 double ureter IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013826 absent hypoglossal canal IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013878 abnormal ductus venosus valve topology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013913 absent costovertebral joint IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013924 abnormal dural venous sinus morphology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013937 absent lobe of thyroid gland IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013952 retroesophageal left subclavian artery IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0014017 abnormal Wolffian duct connection IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0014019 embryo cyst IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1553185 4933434E20Rik RIKEN cDNA 4933434E20 gene gene MP:0020500 persistent trigeminal artery IEA N RGD:5509061 20180628 MGI 1553186 Wdr74 WD repeat domain 74 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1553186 Wdr74 WD repeat domain 74 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1553187 Mia MIA SH3 domain containing gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:11839810 1553189 Crispld2 cysteine-rich secretory protein LCCL domain containing 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200310 MGI 1553189 Crispld2 cysteine-rich secretory protein LCCL domain containing 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200310 MGI 1553189 Crispld2 cysteine-rich secretory protein LCCL domain containing 2 gene MP:0000685 abnormal immune system morphology IEA N RGD:5509061 20200310 MGI 1553189 Crispld2 cysteine-rich secretory protein LCCL domain containing 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200310 MGI 1553189 Crispld2 cysteine-rich secretory protein LCCL domain containing 2 gene MP:0001790 abnormal immune system physiology IEA N RGD:5509061 20200310 MGI 1553189 Crispld2 cysteine-rich secretory protein LCCL domain containing 2 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20200310 MGI 1553189 Crispld2 cysteine-rich secretory protein LCCL domain containing 2 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20200310 MGI 1553189 Crispld2 cysteine-rich secretory protein LCCL domain containing 2 gene MP:0005508 abnormal skeleton morphology IEA N RGD:5509061 20200310 MGI 1553189 Crispld2 cysteine-rich secretory protein LCCL domain containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200310 MGI 1553189 Crispld2 cysteine-rich secretory protein LCCL domain containing 2 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1553192 Pdia3 protein disulfide isomerase associated 3 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20200310 MGI PMID:20576531 1553192 Pdia3 protein disulfide isomerase associated 3 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20230119 MGI 1553192 Pdia3 protein disulfide isomerase associated 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:20022947 1553192 Pdia3 protein disulfide isomerase associated 3 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20200310 MGI PMID:16311600 1553192 Pdia3 protein disulfide isomerase associated 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:20022947 1553192 Pdia3 protein disulfide isomerase associated 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:21941299 1553192 Pdia3 protein disulfide isomerase associated 3 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:20576531 1553192 Pdia3 protein disulfide isomerase associated 3 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20200310 MGI PMID:20576531 1553192 Pdia3 protein disulfide isomerase associated 3 gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20200310 MGI PMID:20576531 1553192 Pdia3 protein disulfide isomerase associated 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16311600 1553192 Pdia3 protein disulfide isomerase associated 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20576531 1553192 Pdia3 protein disulfide isomerase associated 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20022947 1553192 Pdia3 protein disulfide isomerase associated 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1553193 Smchd1 SMC hinge domain containing 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20230119 MGI 1553193 Smchd1 SMC hinge domain containing 1 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20230119 MGI 1553193 Smchd1 SMC hinge domain containing 1 gene MP:0003136 yellow coat color IAGP N RGD:5509061 20200310 MGI PMID:15890782 1553193 Smchd1 SMC hinge domain containing 1 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20200310 MGI PMID:15890782 1553193 Smchd1 SMC hinge domain containing 1 gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20200310 MGI PMID:18425126 1553193 Smchd1 SMC hinge domain containing 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20200310 MGI PMID:18425126 1553193 Smchd1 SMC hinge domain containing 1 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18425126 1553193 Smchd1 SMC hinge domain containing 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20200310 MGI PMID:18425126 1553193 Smchd1 SMC hinge domain containing 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1553193 Smchd1 SMC hinge domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1553193 Smchd1 SMC hinge domain containing 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18425126 1553193 Smchd1 SMC hinge domain containing 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15890782 1553193 Smchd1 SMC hinge domain containing 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18425126 1553193 Smchd1 SMC hinge domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230119 MGI 1553197 Klc1 kinesin light chain 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20180215 MGI 1553197 Klc1 kinesin light chain 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10491391 1553197 Klc1 kinesin light chain 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10491391 1553197 Klc1 kinesin light chain 1 gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20141003 MGI PMID:19420244 1553197 Klc1 kinesin light chain 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:15731448 1553197 Klc1 kinesin light chain 1 gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20141003 MGI PMID:19420244 1553197 Klc1 kinesin light chain 1 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:19420244 1553197 Klc1 kinesin light chain 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:15731448 1553197 Klc1 kinesin light chain 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19420244 1553197 Klc1 kinesin light chain 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:19420244 1553197 Klc1 kinesin light chain 1 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:19420244 1553197 Klc1 kinesin light chain 1 gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:19420244 1553197 Klc1 kinesin light chain 1 gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20141003 MGI PMID:21335237 1553199 Trim10 tripartite motif-containing 10 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 1553199 Trim10 tripartite motif-containing 10 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20240523 MGI 1553199 Trim10 tripartite motif-containing 10 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20210708 MGI PMID:32343488 1553199 Trim10 tripartite motif-containing 10 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 1553199 Trim10 tripartite motif-containing 10 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1553201 Fmn1 formin 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20200310 MGI PMID:7517224 1553201 Fmn1 formin 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20200310 MGI PMID:9234242 1553201 Fmn1 formin 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20200310 MGI PMID:9848078 1553201 Fmn1 formin 1 gene MP:0000536 hydroureter IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0000547 short limbs IEA N RGD:5509061 20111116 MGI 1553201 Fmn1 formin 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20200310 MGI PMID:2997621 1553201 Fmn1 formin 1 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20200310 MGI PMID:17554679 1553201 Fmn1 formin 1 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20200310 MGI PMID:2997621 1553201 Fmn1 formin 1 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20200310 MGI PMID:2997621 1553201 Fmn1 formin 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20200310 MGI PMID:15198975 1553201 Fmn1 formin 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20200310 MGI PMID:2997621 1553201 Fmn1 formin 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20221027 MGI PMID:34548488 1553201 Fmn1 formin 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20200310 MGI PMID:15198975 1553201 Fmn1 formin 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20200310 MGI PMID:19383632 1553201 Fmn1 formin 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20200310 MGI PMID:2997621 1553201 Fmn1 formin 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20221027 MGI PMID:34548488 1553201 Fmn1 formin 1 gene MP:0000566 synostosis IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20200310 MGI PMID:17554679 1553201 Fmn1 formin 1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20200310 MGI PMID:19383632 1553201 Fmn1 formin 1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 1553201 Fmn1 formin 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20200310 MGI PMID:15198975 1553201 Fmn1 formin 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20200310 MGI PMID:17554679 1553201 Fmn1 formin 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20200310 MGI PMID:15198975 1553201 Fmn1 formin 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:7517224 1553201 Fmn1 formin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15198975 1553201 Fmn1 formin 1 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20200310 MGI PMID:2997621 1553201 Fmn1 formin 1 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20200310 MGI PMID:17554679 1553201 Fmn1 formin 1 gene MP:0003073 abnormal metacarpal bone morphology IEA N RGD:5509061 20111116 MGI 1553201 Fmn1 formin 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0003586 dilated ureter IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20200310 MGI PMID:19383632 1553201 Fmn1 formin 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20200310 MGI PMID:7517224 1553201 Fmn1 formin 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20200310 MGI PMID:9234242 1553201 Fmn1 formin 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20200310 MGI PMID:9848078 1553201 Fmn1 formin 1 gene MP:0003722 absent ureter IAGP N RGD:5509061 20200310 MGI PMID:9234242 1553201 Fmn1 formin 1 gene MP:0004356 radius hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0004639 fused metacarpal bones IAGP N RGD:5509061 20200310 MGI PMID:2997621 1553201 Fmn1 formin 1 gene MP:0004642 fused metatarsal bones IAGP N RGD:5509061 20200310 MGI PMID:19383632 1553201 Fmn1 formin 1 gene MP:0004642 fused metatarsal bones IAGP N RGD:5509061 20200310 MGI PMID:2997621 1553201 Fmn1 formin 1 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20200310 MGI PMID:17554679 1553201 Fmn1 formin 1 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0005353 abnormal patella morphology IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0005371 limbs/digits/tail phenotype IAGP N RGD:5509061 20221027 MGI PMID:34548488 1553201 Fmn1 formin 1 gene MP:0005409 darkened coat color IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0005430 absent fibula IAGP N RGD:5509061 20200310 MGI PMID:17554679 1553201 Fmn1 formin 1 gene MP:0005430 absent fibula IAGP N RGD:5509061 20200310 MGI PMID:19383632 1553201 Fmn1 formin 1 gene MP:0005430 absent fibula IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:18560567 1553201 Fmn1 formin 1 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20200310 MGI PMID:19383632 1553201 Fmn1 formin 1 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20200310 MGI PMID:9234242 1553201 Fmn1 formin 1 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20200310 MGI PMID:2997621 1553201 Fmn1 formin 1 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20200310 MGI PMID:2997621 1553201 Fmn1 formin 1 gene MP:0008919 fused tarsal bones IAGP N RGD:5509061 20200310 MGI PMID:2320577 1553201 Fmn1 formin 1 gene MP:0008919 fused tarsal bones IAGP N RGD:5509061 20200310 MGI PMID:2997621 1553201 Fmn1 formin 1 gene MP:0009728 abnormal calcaneum morphology IAGP N RGD:5509061 20200310 MGI PMID:17554679 1553201 Fmn1 formin 1 gene MP:0011090 perinatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1553201 Fmn1 formin 1 gene MP:0011530 fused radius and ulna IAGP N RGD:5509061 20200310 MGI PMID:2997621 1553201 Fmn1 formin 1 gene MP:0011797 blind ureter IAGP N RGD:5509061 20200310 MGI PMID:9234242 1553201 Fmn1 formin 1 gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:34548488 1553201 Fmn1 formin 1 gene MP:0014320 abnormal autopod rotation IAGP N RGD:5509061 20240404 MGI PMID:17554679 1553201 Fmn1 formin 1 gene MP:0014320 abnormal autopod rotation IAGP N RGD:5509061 20240404 MGI PMID:2320577 1553205 Skor1 SKI family transcriptional corepressor 1 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20230601 MGI 1553205 Skor1 SKI family transcriptional corepressor 1 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1553205 Skor1 SKI family transcriptional corepressor 1 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1553205 Skor1 SKI family transcriptional corepressor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1553207 Dmrt1 doublesex and mab-3 related transcription factor 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11040213 1553207 Dmrt1 doublesex and mab-3 related transcription factor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11040213 1553207 Dmrt1 doublesex and mab-3 related transcription factor 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11040213 1553207 Dmrt1 doublesex and mab-3 related transcription factor 1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11040213 1553207 Dmrt1 doublesex and mab-3 related transcription factor 1 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:11040213 1553207 Dmrt1 doublesex and mab-3 related transcription factor 1 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:17540358 1553207 Dmrt1 doublesex and mab-3 related transcription factor 1 gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20141003 MGI PMID:17540358 1553207 Dmrt1 doublesex and mab-3 related transcription factor 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:11040213 1553207 Dmrt1 doublesex and mab-3 related transcription factor 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:17540358 1553207 Dmrt1 doublesex and mab-3 related transcription factor 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:11040213 1553207 Dmrt1 doublesex and mab-3 related transcription factor 1 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:17540358 1553207 Dmrt1 doublesex and mab-3 related transcription factor 1 gene MP:0031407 increased Sertoli cell proliferation IAGP N RGD:5509061 20220630 MGI PMID:11040213 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20240822 MGI PMID:37341808 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:12221714 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:15030764 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:16502419 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:14724733 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20240822 MGI PMID:37341808 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20220519 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:15030764 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20220519 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:15030764 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:17868088 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:11350121 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:14597577 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:14724733 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:15030764 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:17868088 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:8988167 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20240822 MGI PMID:37341808 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20220519 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20220519 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:17652354 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12553906 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11350121 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:14724733 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17868088 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:7729687 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11350121 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:7729687 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20240822 MGI PMID:37341808 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17868088 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:12221714 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20220519 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0002115 abnormal limb bone morphology IEA N RGD:5509061 20111222 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20220519 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0003417 premature endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15030764 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220519 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15030764 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0004378 frontal bone foramen IAGP N RGD:5509061 20141003 MGI PMID:14597577 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0004386 enlarged interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:8988167 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0004424 temporal bone hypoplasia IAGP N RGD:5509061 20171207 MGI PMID:12221714 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20220519 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20220519 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:12553906 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0005270 abnormal zygomatic bone morphology IEA N RGD:5509061 20220519 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15030764 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15030764 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:15030764 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0008430 short temporal bone squamous part IAGP N RGD:5509061 20141003 MGI PMID:17868088 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20240822 MGI PMID:37341808 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220519 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220519 MGI 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15030764 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12553906 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11350121 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7729687 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20240822 MGI PMID:37341808 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14724733 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0013546 cleft soft palate IAGP N RGD:5509061 20240822 MGI PMID:37341808 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171207 MGI PMID:12221714 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171207 MGI PMID:15030764 1553211 Twist1 twist basic helix-loop-helix transcription factor 1 gene MP:0030356 premature lambdoid suture closure IAGP N RGD:5509061 20171207 MGI PMID:15030764 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20240509 MGI PMID:35794642 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20240509 MGI PMID:35794642 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20240509 MGI PMID:35794642 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20240509 MGI PMID:35794642 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20240509 MGI PMID:35794642 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20240509 MGI PMID:35794642 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20240509 MGI PMID:35794642 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20240509 MGI PMID:35794642 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20240509 MGI PMID:35794642 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200310 MGI 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20240509 MGI PMID:35794642 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20240509 MGI PMID:35794642 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20240509 MGI PMID:35794642 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20240509 MGI PMID:35794642 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20240509 MGI PMID:35794642 1553213 Fars2 phenylalanine-tRNA synthetase 2, mitochondrial gene MP:0014246 decreased cellular ATP level IAGP N RGD:5509061 20240509 MGI PMID:35794642 1553214 Stx16 syntaxin 16 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1553214 Stx16 syntaxin 16 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1553214 Stx16 syntaxin 16 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:17317779 1553214 Stx16 syntaxin 16 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1553214 Stx16 syntaxin 16 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1553214 Stx16 syntaxin 16 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200310 MGI 1553214 Stx16 syntaxin 16 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20200310 MGI 1553214 Stx16 syntaxin 16 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 1553214 Stx16 syntaxin 16 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1553214 Stx16 syntaxin 16 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1553214 Stx16 syntaxin 16 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20220811 MGI 1553214 Stx16 syntaxin 16 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1553214 Stx16 syntaxin 16 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20220519 MGI 1553214 Stx16 syntaxin 16 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1553214 Stx16 syntaxin 16 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1553215 Med31 mediator complex subunit 31 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20200310 MGI PMID:20347762 1553215 Med31 mediator complex subunit 31 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:20347762 1553215 Med31 mediator complex subunit 31 gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:12955145 1553215 Med31 mediator complex subunit 31 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:20347762 1553215 Med31 mediator complex subunit 31 gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:12955145 1553215 Med31 mediator complex subunit 31 gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:20347762 1553215 Med31 mediator complex subunit 31 gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20200310 MGI PMID:12955145 1553215 Med31 mediator complex subunit 31 gene MP:0003054 spina bifida IAGP N RGD:5509061 20200310 MGI PMID:20347762 1553215 Med31 mediator complex subunit 31 gene MP:0003717 pallor IAGP N RGD:5509061 20200310 MGI PMID:20347762 1553215 Med31 mediator complex subunit 31 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:12955145 1553215 Med31 mediator complex subunit 31 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:20347762 1553215 Med31 mediator complex subunit 31 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200310 MGI PMID:20347762 1553215 Med31 mediator complex subunit 31 gene MP:0005352 small cranium IAGP N RGD:5509061 20200310 MGI PMID:20347762 1553215 Med31 mediator complex subunit 31 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:20347762 1553215 Med31 mediator complex subunit 31 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20200310 MGI PMID:20347762 1553215 Med31 mediator complex subunit 31 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20200310 MGI PMID:20347762 1553215 Med31 mediator complex subunit 31 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12955145 1553215 Med31 mediator complex subunit 31 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20347762 1553215 Med31 mediator complex subunit 31 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:20347762 1553215 Med31 mediator complex subunit 31 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20200310 MGI PMID:20347762 1553217 Rdx radixin gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:15314067 1553217 Rdx radixin gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12068294 1553217 Rdx radixin gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1553217 Rdx radixin gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15314067 1553217 Rdx radixin gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:12068294 1553217 Rdx radixin gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15314067 1553217 Rdx radixin gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15314067 1553217 Rdx radixin gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15314067 1553217 Rdx radixin gene MP:0004528 fused outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:15314067 1553217 Rdx radixin gene MP:0004531 short outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:15314067 1553217 Rdx radixin gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15314067 1553217 Rdx radixin gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:15314067 1553217 Rdx radixin gene MP:0004536 short inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:15314067 1553217 Rdx radixin gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:12068294 1553217 Rdx radixin gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:12068294 1553217 Rdx radixin gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1553217 Rdx radixin gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:15314067 1553217 Rdx radixin gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12068294 1553217 Rdx radixin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1553217 Rdx radixin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15314067 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0000592 short tail IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0000692 small spleen IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0000706 small thymus IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553218 Pole3 polymerase (DNA directed), epsilon 3 (p17 subunit) gene MP:0014180 abnormal thymus apoptosis IAGP N RGD:5509061 20210128 MGI PMID:32553171 1553219 Zfyve27 zinc finger, FYVE domain containing 27 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210617 MGI PMID:33172474 1553219 Zfyve27 zinc finger, FYVE domain containing 27 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210617 MGI PMID:33172474 1553219 Zfyve27 zinc finger, FYVE domain containing 27 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20210617 MGI PMID:33172474 1553219 Zfyve27 zinc finger, FYVE domain containing 27 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20210617 MGI PMID:33172474 1553219 Zfyve27 zinc finger, FYVE domain containing 27 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20210617 MGI PMID:33172474 1553219 Zfyve27 zinc finger, FYVE domain containing 27 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20210617 MGI PMID:33172474 1553219 Zfyve27 zinc finger, FYVE domain containing 27 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20210617 MGI PMID:33172474 1553220 Rab27b RAB27B, member RAS oncogene family gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:17761531 1553220 Rab27b RAB27B, member RAS oncogene family gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17761531 1553220 Rab27b RAB27B, member RAS oncogene family gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17761531 1553220 Rab27b RAB27B, member RAS oncogene family gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:17384153 1553220 Rab27b RAB27B, member RAS oncogene family gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:17384153 1553220 Rab27b RAB27B, member RAS oncogene family gene MP:0008327 abnormal corticotroph morphology IAGP N RGD:5509061 20141003 MGI PMID:17761531 1553220 Rab27b RAB27B, member RAS oncogene family gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20141003 MGI PMID:17384153 1553220 Rab27b RAB27B, member RAS oncogene family gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:17384153 1553220 Rab27b RAB27B, member RAS oncogene family gene MP:0010809 abnormal club cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21160031 1553220 Rab27b RAB27B, member RAS oncogene family gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20141003 MGI PMID:21160031 1553220 Rab27b RAB27B, member RAS oncogene family gene MP:0010943 abnormal bronchus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21160031 1553220 Rab27b RAB27B, member RAS oncogene family gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20220519 MGI 1553220 Rab27b RAB27B, member RAS oncogene family gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170720 MGI PMID:17384153 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0000315 hemoglobinuria IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0000746 weakness IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0001195 flaky skin IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20201022 MGI 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0002708 nephrolithiasis IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0003606 kidney failure IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0003622 ischuria IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20211021 MGI 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0008822 decreased blood uric acid level IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0009552 urinary bladder obstruction IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0011419 erythrocyturia IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0011424 decreased urine uric acid level IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0011625 cystolithiasis IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0020400 cystinuria IAGP N RGD:5509061 20170803 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0031479 increased urine xanthine level IAGP N RGD:5509061 20230810 MGI PMID:27138983 1553221 Mocs2 molybdenum cofactor synthesis 2 gene MP:0031484 increased urine hypoxanthine level IAGP N RGD:5509061 20230810 MGI PMID:27138983 1553224 Dus2 dihydrouridine synthase 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200514 MGI 1553224 Dus2 dihydrouridine synthase 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200514 MGI 1553224 Dus2 dihydrouridine synthase 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:10639148 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20200310 MGI PMID:12444148 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:12444148 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:10899911 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:10899911 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:16717117 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:16861683 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:16984919 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:18493980 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:16429160 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:16861683 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:18493980 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:7859282 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20200310 MGI PMID:12444148 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200310 MGI PMID:7535475 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20200310 MGI PMID:11298831 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:14663141 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:10639148 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0003606 kidney failure IAGP N RGD:5509061 20200310 MGI PMID:11342578 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0003606 kidney failure IAGP N RGD:5509061 20200310 MGI PMID:15644489 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20200310 MGI PMID:11342578 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20200310 MGI PMID:15644489 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20200310 MGI PMID:23090995 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200310 MGI PMID:10452974 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20200310 MGI PMID:14645573 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20221215 MGI 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20200310 MGI PMID:15644489 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20210128 MGI 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:10899911 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:28636595 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20200310 MGI PMID:10532634 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20200310 MGI PMID:11376856 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:9015751 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20200310 MGI PMID:21565393 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20200310 MGI PMID:7859282 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20200310 MGI PMID:7535475 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:10491411 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20200310 MGI PMID:10491411 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20200310 MGI PMID:7859282 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20200310 MGI PMID:22002608 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008639 decreased circulating interleukin-1 alpha level IAGP N RGD:5509061 20200310 MGI PMID:22002608 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008639 decreased circulating interleukin-1 alpha level IAGP N RGD:5509061 20200310 MGI PMID:7859282 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008639 decreased circulating interleukin-1 alpha level IAGP N RGD:5509061 20200310 MGI PMID:9491891 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20200310 MGI PMID:22002608 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20200310 MGI PMID:7859282 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20200310 MGI PMID:9491891 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20200310 MGI PMID:14693703 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20200310 MGI PMID:22002608 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20200310 MGI PMID:7535475 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20200310 MGI PMID:7859282 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:14663141 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:14693703 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:18493980 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:20457908 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:22002608 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:29472103 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:7535475 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:7859282 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:9809553 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20200310 MGI PMID:10491411 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20200310 MGI PMID:14693703 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20200310 MGI PMID:22002608 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20200310 MGI PMID:29472103 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20200310 MGI PMID:7535475 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20200310 MGI PMID:16407889 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20200310 MGI PMID:22002608 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20200310 MGI PMID:7859282 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20200310 MGI PMID:9015751 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20200310 MGI PMID:9317135 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20200310 MGI PMID:9491891 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20200310 MGI PMID:16717117 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:7535475 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:16717117 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:10639148 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:22002608 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:18493980 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:10899911 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20200310 MGI PMID:21565393 1553228 Casp4 caspase 4, apoptosis-related cysteine peptidase gene MP:0011081 decreased macrophage apoptosis IAGP N RGD:5509061 20200310 MGI PMID:22002608 1553230 Mc2r melanocortin 2 receptor gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0000640 adrenal gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20141003 MGI 1553230 Mc2r melanocortin 2 receptor gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0002906 increased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20141003 MGI 1553230 Mc2r melanocortin 2 receptor gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0005459 decreased percent body fat/body weight IEA N RGD:5509061 20141003 MGI 1553230 Mc2r melanocortin 2 receptor gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0005661 decreased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0008294 abnormal adrenal gland zona fasciculata morphology IAGP N RGD:5509061 20150305 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0008299 adrenal cortical hyperplasia IEA N RGD:5509061 20141003 MGI 1553230 Mc2r melanocortin 2 receptor gene MP:0009137 decreased brown fat lipid droplet number IEA N RGD:5509061 20141003 MGI 1553230 Mc2r melanocortin 2 receptor gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0013565 abnormal adrenal gland capsule morphology IAGP N RGD:5509061 20150305 MGI PMID:17989225 1553230 Mc2r melanocortin 2 receptor gene MP:0031391 increased locomotor activity IEA N RGD:5509061 20220421 MGI 1553231 Cnr2 cannabinoid receptor 2 gene MP:0000414 alopecia IEA N RGD:5509061 20111116 MGI 1553231 Cnr2 cannabinoid receptor 2 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210520 MGI 1553231 Cnr2 cannabinoid receptor 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1553231 Cnr2 cannabinoid receptor 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1553231 Cnr2 cannabinoid receptor 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1553231 Cnr2 cannabinoid receptor 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1553231 Cnr2 cannabinoid receptor 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10822068 1553231 Cnr2 cannabinoid receptor 2 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1553231 Cnr2 cannabinoid receptor 2 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20210520 MGI 1553231 Cnr2 cannabinoid receptor 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1553233 Tspan9 tetraspanin 9 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20210722 MGI PMID:34048705 1553233 Tspan9 tetraspanin 9 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20210722 MGI PMID:34048705 1553233 Tspan9 tetraspanin 9 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1553233 Tspan9 tetraspanin 9 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20210722 MGI PMID:34048705 1553233 Tspan9 tetraspanin 9 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1553233 Tspan9 tetraspanin 9 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:21228155 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:21228155 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0001504 abnormal posture IAGP N RGD:5509061 20200310 MGI PMID:21228155 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20200310 MGI PMID:15989966 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:15989966 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20200310 MGI PMID:15989966 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200310 MGI PMID:21228155 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:15989966 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200310 MGI PMID:21228155 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20200310 MGI PMID:21228155 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:21228155 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:15989966 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0005424 jerky movement IAGP N RGD:5509061 20200310 MGI PMID:21228155 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:28360124 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20200310 MGI PMID:21228155 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20200310 MGI PMID:21228155 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:21228155 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200310 MGI PMID:21228155 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0008830 abnormal nucleolus morphology IAGP N RGD:5509061 20200310 MGI PMID:21228155 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0008830 abnormal nucleolus morphology IAGP N RGD:5509061 20200310 MGI PMID:28360124 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15989966 1553236 Rrn3 RRN3 RNA polymerase I transcription factor homolog (yeast) gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20200310 MGI PMID:15989966 1553237 Krt86 keratin 86 gene MP:0001200 thick skin IEA N RGD:5509061 20210128 MGI 1553237 Krt86 keratin 86 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1553238 Tacstd2 tumor-associated calcium signal transducer 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20201022 MGI 1553238 Tacstd2 tumor-associated calcium signal transducer 2 gene MP:0001147 small testis IEA N RGD:5509061 20201022 MGI 1553238 Tacstd2 tumor-associated calcium signal transducer 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1553238 Tacstd2 tumor-associated calcium signal transducer 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1553238 Tacstd2 tumor-associated calcium signal transducer 2 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21970857 1553238 Tacstd2 tumor-associated calcium signal transducer 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1553238 Tacstd2 tumor-associated calcium signal transducer 2 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:21970857 1553238 Tacstd2 tumor-associated calcium signal transducer 2 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20141003 MGI PMID:21970857 1553238 Tacstd2 tumor-associated calcium signal transducer 2 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21970857 1553238 Tacstd2 tumor-associated calcium signal transducer 2 gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21970857 1553238 Tacstd2 tumor-associated calcium signal transducer 2 gene MP:0010367 increased spindle cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21970857 1553238 Tacstd2 tumor-associated calcium signal transducer 2 gene MP:0012193 increased keratinocyte migration IAGP N RGD:5509061 20141204 MGI PMID:21970857 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:12801998 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10733589 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12801998 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10733589 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:12801998 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:12801998 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10733589 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12801998 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10733589 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:10733589 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:10733589 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:12801998 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:10733589 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:10733589 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:12801998 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:12801998 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0014468 disorganized sperm mitochondrial sheath IAGP N RGD:5509061 20240613 MGI PMID:10733589 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:12801998 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20200227 MGI PMID:12801998 1553240 Nectin2 nectin cell adhesion molecule 2 gene MP:0031389 abnormal ectoplasmic specialization morphology IAGP N RGD:5509061 20220428 MGI PMID:12801998 1553242 Alk anaplastic lymphoma kinase gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20160304 MGI PMID:25955180 1553242 Alk anaplastic lymphoma kinase gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20160915 MGI PMID:24811913 1553242 Alk anaplastic lymphoma kinase gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20201217 MGI PMID:31218818 1553242 Alk anaplastic lymphoma kinase gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20160915 MGI PMID:24811913 1553242 Alk anaplastic lymphoma kinase gene MP:0001013 enlarged superior cervical ganglion IAGP N RGD:5509061 20160915 MGI PMID:24811913 1553242 Alk anaplastic lymphoma kinase gene MP:0001013 enlarged superior cervical ganglion IAGP N RGD:5509061 20201217 MGI PMID:31218818 1553242 Alk anaplastic lymphoma kinase gene MP:0001017 abnormal stellate ganglion morphology IAGP N RGD:5509061 20160915 MGI PMID:24811913 1553242 Alk anaplastic lymphoma kinase gene MP:0001017 abnormal stellate ganglion morphology IAGP N RGD:5509061 20201217 MGI PMID:31218818 1553242 Alk anaplastic lymphoma kinase gene MP:0001147 small testis IAGP N RGD:5509061 20160304 MGI PMID:25955180 1553242 Alk anaplastic lymphoma kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160304 MGI PMID:25955180 1553242 Alk anaplastic lymphoma kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0001752 abnormal hypothalamus secretion IAGP N RGD:5509061 20160304 MGI PMID:25955180 1553242 Alk anaplastic lymphoma kinase gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20160304 MGI PMID:25955180 1553242 Alk anaplastic lymphoma kinase gene MP:0001957 apnea IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0002039 increased neuroblastoma incidence IAGP N RGD:5509061 20160915 MGI PMID:24811913 1553242 Alk anaplastic lymphoma kinase gene MP:0002039 increased neuroblastoma incidence IAGP N RGD:5509061 20180920 MGI PMID:29321660 1553242 Alk anaplastic lymphoma kinase gene MP:0002039 increased neuroblastoma incidence IAGP N RGD:5509061 20201217 MGI PMID:31218818 1553242 Alk anaplastic lymphoma kinase gene MP:0002083 premature death IAGP N RGD:5509061 20180920 MGI PMID:29321660 1553242 Alk anaplastic lymphoma kinase gene MP:0002083 premature death IAGP N RGD:5509061 20201217 MGI PMID:31218818 1553242 Alk anaplastic lymphoma kinase gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201217 MGI PMID:31218818 1553242 Alk anaplastic lymphoma kinase gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20160304 MGI PMID:25955180 1553242 Alk anaplastic lymphoma kinase gene MP:0002673 abnormal sperm number IAGP N RGD:5509061 20160304 MGI PMID:25955180 1553242 Alk anaplastic lymphoma kinase gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20160304 MGI PMID:25955180 1553242 Alk anaplastic lymphoma kinase gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20160225 MGI PMID:21799923 1553242 Alk anaplastic lymphoma kinase gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20160304 MGI PMID:25955180 1553242 Alk anaplastic lymphoma kinase gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20160304 MGI PMID:25955180 1553242 Alk anaplastic lymphoma kinase gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20160304 MGI PMID:25955180 1553242 Alk anaplastic lymphoma kinase gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20160304 MGI PMID:25955180 1553242 Alk anaplastic lymphoma kinase gene MP:0008940 delayed balanopreputial separation IAGP N RGD:5509061 20160304 MGI PMID:25955180 1553242 Alk anaplastic lymphoma kinase gene MP:0008975 delayed male fertility IAGP N RGD:5509061 20160304 MGI PMID:25955180 1553242 Alk anaplastic lymphoma kinase gene MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20160225 MGI PMID:21799923 1553242 Alk anaplastic lymphoma kinase gene MP:0010052 increased grip strength IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0010232 delayed skin pigmentation appearance IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20201217 MGI PMID:31218818 1553242 Alk anaplastic lymphoma kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0011940 decreased food intake IAGP N RGD:5509061 20160915 MGI PMID:24811761 1553242 Alk anaplastic lymphoma kinase gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20160304 MGI PMID:25955180 1553242 Alk anaplastic lymphoma kinase gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:31218818 1553245 Iscu iron-sulfur cluster assembly enzyme gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20230907 MGI PMID:21165651 1553246 Art2b ADP-ribosyltransferase 2b gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:16585549 1553246 Art2b ADP-ribosyltransferase 2b gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16585549 1553247 Adgrl3 adhesion G protein-coupled receptor L3 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20190718 MGI PMID:27247960 1553247 Adgrl3 adhesion G protein-coupled receptor L3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22575564 1553247 Adgrl3 adhesion G protein-coupled receptor L3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22575564 1553247 Adgrl3 adhesion G protein-coupled receptor L3 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:22575564 1553247 Adgrl3 adhesion G protein-coupled receptor L3 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20190718 MGI PMID:27247960 1553247 Adgrl3 adhesion G protein-coupled receptor L3 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22575564 1553247 Adgrl3 adhesion G protein-coupled receptor L3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1553247 Adgrl3 adhesion G protein-coupled receptor L3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20220505 MGI PMID:30792275 1553247 Adgrl3 adhesion G protein-coupled receptor L3 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20190718 MGI PMID:27247960 1553247 Adgrl3 adhesion G protein-coupled receptor L3 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20190718 MGI PMID:27247960 1553247 Adgrl3 adhesion G protein-coupled receptor L3 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22575564 1553247 Adgrl3 adhesion G protein-coupled receptor L3 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:22575564 1553247 Adgrl3 adhesion G protein-coupled receptor L3 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:22575564 1553247 Adgrl3 adhesion G protein-coupled receptor L3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:27247960 1553252 Mdfic MyoD family inhibitor domain containing gene MP:0001505 hunched posture IAGP N RGD:5509061 20220804 MGI PMID:35235341 1553252 Mdfic MyoD family inhibitor domain containing gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20220804 MGI PMID:35235341 1553252 Mdfic MyoD family inhibitor domain containing gene MP:0001954 respiratory distress IAGP N RGD:5509061 20220804 MGI PMID:35235341 1553252 Mdfic MyoD family inhibitor domain containing gene MP:0002083 premature death IAGP N RGD:5509061 20220804 MGI PMID:35235341 1553252 Mdfic MyoD family inhibitor domain containing gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20220804 MGI PMID:35235341 1553252 Mdfic MyoD family inhibitor domain containing gene MP:0003660 chylothorax IAGP N RGD:5509061 20220804 MGI PMID:35235341 1553252 Mdfic MyoD family inhibitor domain containing gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20220804 MGI PMID:35235341 1553252 Mdfic MyoD family inhibitor domain containing gene MP:0031392 hypoactivity IAGP N RGD:5509061 20220804 MGI PMID:35235341 1553253 Nsun6 NOL1/NOP2/Sun domain family member 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:33330931 1553255 Klhl18 kelch-like 18 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1553255 Klhl18 kelch-like 18 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1553255 Klhl18 kelch-like 18 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1553255 Klhl18 kelch-like 18 gene MP:0004415 abnormal cochlear nerve compound action potential IAGP N RGD:5509061 20211021 MGI PMID:34597341 1553255 Klhl18 kelch-like 18 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20211021 MGI PMID:34597341 1553255 Klhl18 kelch-like 18 gene MP:0010052 increased grip strength IEA N RGD:5509061 20200310 MGI 1553255 Klhl18 kelch-like 18 gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20211021 MGI 1553255 Klhl18 kelch-like 18 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20211021 MGI PMID:34597341 1553256 Ranbp10 RAN binding protein 10 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20200310 MGI PMID:19801445 1553256 Ranbp10 RAN binding protein 10 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1553256 Ranbp10 RAN binding protein 10 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200310 MGI 1553256 Ranbp10 RAN binding protein 10 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20200310 MGI PMID:19801445 1553256 Ranbp10 RAN binding protein 10 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:19801445 1553256 Ranbp10 RAN binding protein 10 gene MP:0003405 abnormal platelet shape IAGP N RGD:5509061 20200310 MGI PMID:19801445 1553256 Ranbp10 RAN binding protein 10 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20200310 MGI 1553256 Ranbp10 RAN binding protein 10 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20200310 MGI PMID:19801445 1553256 Ranbp10 RAN binding protein 10 gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20200310 MGI PMID:19801445 1553256 Ranbp10 RAN binding protein 10 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20200310 MGI PMID:19801445 1553257 Zmynd8 zinc finger, MYND-type containing 8 gene MP:0001262 decreased body weight IEA N RGD:5509061 20200310 MGI 1553257 Zmynd8 zinc finger, MYND-type containing 8 gene MP:0001539 decreased caudal vertebrae number IEA N RGD:5509061 20200310 MGI 1553257 Zmynd8 zinc finger, MYND-type containing 8 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20200310 MGI 1553257 Zmynd8 zinc finger, MYND-type containing 8 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20200310 MGI 1553257 Zmynd8 zinc finger, MYND-type containing 8 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200310 MGI 1553257 Zmynd8 zinc finger, MYND-type containing 8 gene MP:0010093 decreased circulating magnesium level IEA N RGD:5509061 20200310 MGI 1553257 Zmynd8 zinc finger, MYND-type containing 8 gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20230223 MGI PMID:35857506 1553257 Zmynd8 zinc finger, MYND-type containing 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553258 Ttyh3 tweety family member 3 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1553258 Ttyh3 tweety family member 3 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20230119 MGI 1553258 Ttyh3 tweety family member 3 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1553258 Ttyh3 tweety family member 3 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1553258 Ttyh3 tweety family member 3 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20230119 MGI 1553259 Ube2a ubiquitin-conjugating enzyme E2A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15169909 1553259 Ube2a ubiquitin-conjugating enzyme E2A gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1553259 Ube2a ubiquitin-conjugating enzyme E2A gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1553259 Ube2a ubiquitin-conjugating enzyme E2A gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20160310 MGI PMID:26476408 1553259 Ube2a ubiquitin-conjugating enzyme E2A gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 1553259 Ube2a ubiquitin-conjugating enzyme E2A gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15169909 1553259 Ube2a ubiquitin-conjugating enzyme E2A gene MP:0002833 increased heart weight IEA N RGD:5509061 20220811 MGI 1553259 Ube2a ubiquitin-conjugating enzyme E2A gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20240523 MGI 1553259 Ube2a ubiquitin-conjugating enzyme E2A gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20160310 MGI PMID:26476408 1553259 Ube2a ubiquitin-conjugating enzyme E2A gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:15169909 1553259 Ube2a ubiquitin-conjugating enzyme E2A gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1553259 Ube2a ubiquitin-conjugating enzyme E2A gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1553259 Ube2a ubiquitin-conjugating enzyme E2A gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15169909 1553259 Ube2a ubiquitin-conjugating enzyme E2A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15169909 1553259 Ube2a ubiquitin-conjugating enzyme E2A gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20160310 MGI PMID:26476408 1553261 Cachd1 cache domain containing 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20211216 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20211209 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20211216 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20220811 MGI 1553261 Cachd1 cache domain containing 1 gene MP:0001394 circling IAGP N RGD:5509061 20211209 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20211209 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0003144 decreased otolith number IAGP N RGD:5509061 20211209 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20211216 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0003169 abnormal scala media morphology IAGP N RGD:5509061 20211209 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20211216 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20211209 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0004422 small temporal bone IAGP N RGD:5509061 20211216 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20211216 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0004885 abnormal endolymph physiology IAGP N RGD:5509061 20211216 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0004886 increased endolymph production IAGP N RGD:5509061 20211209 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0005191 head tilt IAGP N RGD:5509061 20211209 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20211209 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20211209 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20211209 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0006403 abnormal cochlear endolymph ionic homeostasis IAGP N RGD:5509061 20211216 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1553261 Cachd1 cache domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1553261 Cachd1 cache domain containing 1 gene MP:0011238 abnormal inner ear development IAGP N RGD:5509061 20211216 MGI PMID:34388681 1553261 Cachd1 cache domain containing 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20211209 MGI PMID:34388681 1553262 Tbc1d10c TBC1 domain family, member 10c gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20200310 MGI PMID:23109291 1553262 Tbc1d10c TBC1 domain family, member 10c gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20200310 MGI PMID:23109291 1553262 Tbc1d10c TBC1 domain family, member 10c gene MP:0002493 increased IgG level IAGP N RGD:5509061 20200310 MGI PMID:23109291 1553262 Tbc1d10c TBC1 domain family, member 10c gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:23109291 1553262 Tbc1d10c TBC1 domain family, member 10c gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20200310 MGI PMID:23109291 1553262 Tbc1d10c TBC1 domain family, member 10c gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20200310 MGI PMID:23109291 1553262 Tbc1d10c TBC1 domain family, member 10c gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20200310 MGI PMID:23109291 1553262 Tbc1d10c TBC1 domain family, member 10c gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:23109291 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0004941 abnormal regulatory T cell morphology IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0008087 decreased T helper 1 cell number IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0010740 abnormal dendritic cell chemotaxis IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0013022 increased Ly6C high monocyte number IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553263 Extl1 exostosin-like glycosyltransferase 1 gene MP:0020349 abnormal dendritic cell migration IAGP N RGD:5509061 20240606 MGI PMID:36656709 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20347813 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15825076 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12015290 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22384261 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10431239 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0000765 abnormal tongue squamous epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20347813 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:20347813 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:10431239 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:10431239 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0001297 microphthalmia IAGP N RGD:5509061 20150212 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0001306 small lens IAGP N RGD:5509061 20150212 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0001320 small pupil IAGP N RGD:5509061 20150212 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:10431239 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:10431239 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:22745808 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:15825076 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:20347813 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20150212 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12015290 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20347813 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:20347813 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:18243172 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0002782 abnormal testes secretion IAGP N RGD:5509061 20141003 MGI PMID:18243172 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:10431239 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20150212 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20150806 MGI PMID:21600198 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0003093 abnormal cornea anterior stroma morphology IAGP N RGD:5509061 20150212 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0003285 gastric hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15825076 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:10431239 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22384261 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0003892 abnormal gastric gland morphology IAGP N RGD:5509061 20141003 MGI PMID:15825076 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20141003 MGI PMID:18243172 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0004137 abnormal gastric surface mucous cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15825076 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0004138 abnormal mucous neck cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15825076 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15825076 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20150312 MGI PMID:15825076 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0004481 abnormal conjunctival epithelium morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22491752 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20190307 MGI PMID:27027284 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20150806 MGI PMID:21600198 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0005251 blepharitis IAGP N RGD:5509061 20150212 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20150212 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20150212 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20150212 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0006307 abnormal seminiferous tubule size IAGP N RGD:5509061 20141003 MGI PMID:18243172 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0008521 abnormal Bowman membrane morphology IAGP N RGD:5509061 20150212 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22491752 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22745808 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0009612 thick epidermis suprabasal layer IAGP N RGD:5509061 20141003 MGI PMID:22491752 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0009742 increased cornea stroma thickness IAGP N RGD:5509061 20150212 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0010203 focal ventral hair loss IAGP N RGD:5509061 20141003 MGI PMID:20347813 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:15825076 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10431239 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12015290 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20150212 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18243172 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0012101 acoria IAGP N RGD:5509061 20150212 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0012110 increased hair follicle number IAGP N RGD:5509061 20180607 MGI PMID:22491752 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0012193 increased keratinocyte migration IAGP N RGD:5509061 20141204 MGI PMID:22491752 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0013026 decreased Ly6C low monocyte number IAGP N RGD:5509061 20170413 MGI PMID:27814941 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0013485 increased Paneth cell number IAGP N RGD:5509061 20160310 MGI PMID:22384261 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0013527 absent conjunctiva goblet cells IAGP N RGD:5509061 20150219 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0013527 absent conjunctiva goblet cells IAGP N RGD:5509061 20150806 MGI PMID:21600198 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0013754 abnormal ocular surface morphology IAGP N RGD:5509061 20150806 MGI PMID:21600198 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0013765 iris hyperplasia IAGP N RGD:5509061 20150430 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20150806 MGI PMID:12015290 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0014077 ectopic Paneth cells IAGP N RGD:5509061 20160310 MGI PMID:22384261 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0020862 increased cornea fragility IAGP N RGD:5509061 20181101 MGI PMID:17060454 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0030574 increased hair follicle cell proliferation IAGP N RGD:5509061 20181129 MGI PMID:22745808 1553264 Klf4 Kruppel-like transcription factor 4 (gut) gene MP:0030577 increased keratinocyte adhesion IAGP N RGD:5509061 20180607 MGI PMID:22491752 1553266 Ddx51 DEAD box helicase 51 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1553266 Ddx51 DEAD box helicase 51 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1553266 Ddx51 DEAD box helicase 51 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553270 Smug1 single-strand selective monofunctional uracil DNA glycosylase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22447450 1553270 Smug1 single-strand selective monofunctional uracil DNA glycosylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22447450 1553270 Smug1 single-strand selective monofunctional uracil DNA glycosylase gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:22447450 1553270 Smug1 single-strand selective monofunctional uracil DNA glycosylase gene MP:0009796 abnormal base-excision repair IAGP N RGD:5509061 20141003 MGI PMID:22447450 1553270 Smug1 single-strand selective monofunctional uracil DNA glycosylase gene MP:0009797 abnormal mismatch repair IAGP N RGD:5509061 20141003 MGI PMID:22447450 1553270 Smug1 single-strand selective monofunctional uracil DNA glycosylase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22447450 1553270 Smug1 single-strand selective monofunctional uracil DNA glycosylase gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22447450 1553271 Fblim1 filamin binding LIM protein 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22556421 1553271 Fblim1 filamin binding LIM protein 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22556421 1553271 Fblim1 filamin binding LIM protein 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22556421 1553271 Fblim1 filamin binding LIM protein 1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:22556421 1553271 Fblim1 filamin binding LIM protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21224394 1553271 Fblim1 filamin binding LIM protein 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1553271 Fblim1 filamin binding LIM protein 1 gene MP:0003450 enlarged pancreas IEA N RGD:5509061 20190502 MGI 1553271 Fblim1 filamin binding LIM protein 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:22556421 1553271 Fblim1 filamin binding LIM protein 1 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:22556421 1553271 Fblim1 filamin binding LIM protein 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22556421 1553271 Fblim1 filamin binding LIM protein 1 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:22556421 1553271 Fblim1 filamin binding LIM protein 1 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:22556421 1553271 Fblim1 filamin binding LIM protein 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:22556421 1553271 Fblim1 filamin binding LIM protein 1 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:22556421 1553273 Amigo2 adhesion molecule with Ig like domain 2 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20201224 MGI PMID:31693896 1553273 Amigo2 adhesion molecule with Ig like domain 2 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20201224 MGI PMID:31693896 1553273 Amigo2 adhesion molecule with Ig like domain 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1553273 Amigo2 adhesion molecule with Ig like domain 2 gene MP:0020376 abnormal starburst amacrine cell morphology IAGP N RGD:5509061 20201224 MGI PMID:31693896 1553275 Hoxc6 homeobox C6 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:17626057 1553275 Hoxc6 homeobox C6 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:11002345 1553275 Hoxc6 homeobox C6 gene MP:0001881 abnormal mammary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:11002345 1553275 Hoxc6 homeobox C6 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:11002345 1553275 Hoxc6 homeobox C6 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1553275 Hoxc6 homeobox C6 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:17626057 1553275 Hoxc6 homeobox C6 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:17626057 1553275 Hoxc6 homeobox C6 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1553275 Hoxc6 homeobox C6 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1553275 Hoxc6 homeobox C6 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11002345 1553275 Hoxc6 homeobox C6 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1553275 Hoxc6 homeobox C6 gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1553275 Hoxc6 homeobox C6 gene MP:0004680 small xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:17626057 1553275 Hoxc6 homeobox C6 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1553275 Hoxc6 homeobox C6 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:17626057 1553275 Hoxc6 homeobox C6 gene MP:0013711 abnormal inguinal mammary gland morphology IAGP N RGD:5509061 20150402 MGI PMID:11002345 1553275 Hoxc6 homeobox C6 gene MP:0013712 abnormal thoracic mammary gland morphology IAGP N RGD:5509061 20150402 MGI PMID:11002345 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20201231 MGI 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20170105 MGI 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20200213 MGI PMID:31408169 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21209834 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23213375 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23213375 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200213 MGI PMID:31408169 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21209834 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23213375 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0002001 blindness IAGP N RGD:5509061 20200213 MGI PMID:31408169 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21930907 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:21930907 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:23213375 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0003609 small scrotum IAGP N RGD:5509061 20141003 MGI PMID:23213375 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20200213 MGI PMID:31408169 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21209834 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23213375 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:21209834 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:23213375 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21209834 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0005358 abnormal incisor morphology IEA N RGD:5509061 20201231 MGI 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21209834 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21209834 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23213375 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200213 MGI PMID:31408169 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200213 MGI PMID:31408169 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:21930907 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20200213 MGI PMID:31408169 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23213375 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200213 MGI PMID:31408169 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200213 MGI PMID:31408169 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200213 MGI PMID:31408169 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:23213375 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20200213 MGI PMID:31408169 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20200213 MGI PMID:31408169 1553279 Hsp90aa1 heat shock protein 90, alpha (cytosolic), class A member 1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20200213 MGI PMID:31408169 1553280 Hacl1 2-hydroxyacyl-CoA lyase 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1553280 Hacl1 2-hydroxyacyl-CoA lyase 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1553280 Hacl1 2-hydroxyacyl-CoA lyase 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553284 Mtfmt mitochondrial methionyl-tRNA formyltransferase gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20240808 MGI PMID:36983072 1553285 Tgfbi transforming growth factor, beta induced gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19117985 1553285 Tgfbi transforming growth factor, beta induced gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19117985 1553285 Tgfbi transforming growth factor, beta induced gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20200507 MGI PMID:32029872 1553285 Tgfbi transforming growth factor, beta induced gene MP:0001314 cornea opacity IAGP N RGD:5509061 20200507 MGI PMID:32029872 1553285 Tgfbi transforming growth factor, beta induced gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19117985 1553285 Tgfbi transforming growth factor, beta induced gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19117985 1553285 Tgfbi transforming growth factor, beta induced gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19117985 1553285 Tgfbi transforming growth factor, beta induced gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19117985 1553285 Tgfbi transforming growth factor, beta induced gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19117985 1553285 Tgfbi transforming growth factor, beta induced gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20200507 MGI PMID:32029872 1553285 Tgfbi transforming growth factor, beta induced gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20160929 MGI PMID:24728038 1553285 Tgfbi transforming growth factor, beta induced gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19117985 1553285 Tgfbi transforming growth factor, beta induced gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20160929 MGI PMID:24728038 1553285 Tgfbi transforming growth factor, beta induced gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:19117985 1553285 Tgfbi transforming growth factor, beta induced gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:19117985 1553285 Tgfbi transforming growth factor, beta induced gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19117985 1553285 Tgfbi transforming growth factor, beta induced gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20160929 MGI PMID:24728038 1553285 Tgfbi transforming growth factor, beta induced gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20200507 MGI PMID:32029872 1553285 Tgfbi transforming growth factor, beta induced gene MP:0011996 abnormal retina inner nuclear layer thickness IAGP N RGD:5509061 20170504 MGI PMID:26387839 1553285 Tgfbi transforming growth factor, beta induced gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19117985 1553285 Tgfbi transforming growth factor, beta induced gene MP:0014117 increased pancreatic beta cell apoptosis IAGP N RGD:5509061 20160929 MGI PMID:24728038 1553285 Tgfbi transforming growth factor, beta induced gene MP:0020087 increased susceptibility to non-insulin-dependent diabetes IAGP N RGD:5509061 20160929 MGI PMID:24728038 1553285 Tgfbi transforming growth factor, beta induced gene MP:0030006 decreased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:26387839 1553287 Pkn2 protein kinase N2 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1553287 Pkn2 protein kinase N2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1553287 Pkn2 protein kinase N2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20181227 MGI 1553287 Pkn2 protein kinase N2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1553287 Pkn2 protein kinase N2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1553287 Pkn2 protein kinase N2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 1553287 Pkn2 protein kinase N2 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0009328 delayed heart looping IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553287 Pkn2 protein kinase N2 gene MP:0011702 abnormal fibroblast proliferation IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0011897 decreased circulating unsaturated transferrin level IEA N RGD:5509061 20210128 MGI 1553287 Pkn2 protein kinase N2 gene MP:0012176 abnormal head development IAGP N RGD:5509061 20171214 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0013925 abnormal vascular plexus formation IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0014138 abnormal germ layer morphology IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553287 Pkn2 protein kinase N2 gene MP:0014141 abnormal mesoderm morphology IAGP N RGD:5509061 20171109 MGI PMID:26774483 1553288 Zbed3 zinc finger, BED type containing 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20240523 MGI 1553288 Zbed3 zinc finger, BED type containing 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20201112 MGI PMID:28992324 1553288 Zbed3 zinc finger, BED type containing 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 1553288 Zbed3 zinc finger, BED type containing 3 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20201112 MGI PMID:28992324 1553288 Zbed3 zinc finger, BED type containing 3 gene MP:0003718 maternal effect IAGP N RGD:5509061 20201112 MGI PMID:28992324 1553288 Zbed3 zinc finger, BED type containing 3 gene MP:0009709 hydrometra IEA N RGD:5509061 20240523 MGI 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:15499555 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9679067 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:15499555 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:9500603 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:9679067 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:15499555 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:9679067 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:9500603 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:9679067 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9679067 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15499555 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9310465 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9500603 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9679067 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:9679067 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:9679067 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:15499555 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:9500603 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:9679067 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9679067 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9679067 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9679067 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15499555 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0008054 abnormal uterine NK cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15499555 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:12219085 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:9500603 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9500603 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9679067 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0012529 abnormal decidua basalis morphology IAGP N RGD:5509061 20141003 MGI PMID:9500603 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0012530 abnormal decidua capsularis morphology IAGP N RGD:5509061 20141003 MGI PMID:9500603 1553290 Il11ra1 interleukin 11 receptor subunit alpha 1 gene MP:0012530 abnormal decidua capsularis morphology IAGP N RGD:5509061 20141003 MGI PMID:9679067 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20221215 MGI 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0001512 trunk curl IEA N RGD:5509061 20200310 MGI 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0002174 abnormal gastrulation movements IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20200310 MGI PMID:15820682 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20200310 MGI PMID:15820682 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20200310 MGI PMID:15820682 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0012675 enlarged floor plate IAGP N RGD:5509061 20200310 MGI PMID:19379695 1553292 Smurf1 SMAD specific E3 ubiquitin protein ligase 1 gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:15820682 1553293 Apba1 amyloid beta precursor protein binding family A member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17167098 1553293 Apba1 amyloid beta precursor protein binding family A member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12547917 1553293 Apba1 amyloid beta precursor protein binding family A member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17167098 1553293 Apba1 amyloid beta precursor protein binding family A member 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17167098 1553293 Apba1 amyloid beta precursor protein binding family A member 1 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:12103443 1553293 Apba1 amyloid beta precursor protein binding family A member 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17167098 1553293 Apba1 amyloid beta precursor protein binding family A member 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17167098 1553293 Apba1 amyloid beta precursor protein binding family A member 1 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:17167098 1553293 Apba1 amyloid beta precursor protein binding family A member 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12547917 1553293 Apba1 amyloid beta precursor protein binding family A member 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17167098 1553293 Apba1 amyloid beta precursor protein binding family A member 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:12103443 1553293 Apba1 amyloid beta precursor protein binding family A member 1 gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:12103443 1553293 Apba1 amyloid beta precursor protein binding family A member 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17167098 1553294 Qpctl glutaminyl-peptide cyclotransferase-like gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20230323 MGI PMID:35314846 1553294 Qpctl glutaminyl-peptide cyclotransferase-like gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20230323 MGI PMID:35314846 1553294 Qpctl glutaminyl-peptide cyclotransferase-like gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20200310 MGI PMID:21900558 1553294 Qpctl glutaminyl-peptide cyclotransferase-like gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20230323 MGI PMID:35314846 1553296 Os9 amplified in osteosarcoma gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20201231 MGI 1553296 Os9 amplified in osteosarcoma gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201231 MGI 1553296 Os9 amplified in osteosarcoma gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20201231 MGI 1553296 Os9 amplified in osteosarcoma gene MP:0004609 vertebral fusion IEA N RGD:5509061 20170105 MGI 1553298 Tsn translin gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20151112 MGI PMID:18239274 1553298 Tsn translin gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18719666 1553298 Tsn translin gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:12944470 1553298 Tsn translin gene MP:0012734 abnormal response to radiation IAGP N RGD:5509061 20151112 MGI PMID:18239274 1553298 Tsn translin gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:12944470 1553300 Dcaf7 DDB1 and CUL4 associated factor 7 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210520 MGI 1553300 Dcaf7 DDB1 and CUL4 associated factor 7 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 1553300 Dcaf7 DDB1 and CUL4 associated factor 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553300 Dcaf7 DDB1 and CUL4 associated factor 7 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20200310 MGI PMID:8046347 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0000618 small salivary gland IAGP N RGD:5509061 20200310 MGI PMID:7541529 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0000653 abnormal sex gland morphology IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0001142 abnormal vagina orifice morphology IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0001261 obese IAGP N RGD:5509061 20200310 MGI PMID:27534441 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20200310 MGI PMID:21368045 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:7541529 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:8339285 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:8828479 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20200310 MGI PMID:21368045 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0002637 small uterus IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0002669 abnormal scrotum morphology IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20200310 MGI PMID:7541529 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0002785 absent Leydig cells IAGP N RGD:5509061 20200310 MGI PMID:19574395 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20200310 MGI PMID:7541529 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20200310 MGI PMID:21368045 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20200310 MGI PMID:7541529 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20200310 MGI PMID:21368045 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20200310 MGI PMID:7541529 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20200310 MGI PMID:21368045 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200310 MGI PMID:8046347 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0005128 decreased adrenocorticotropin level IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0005138 decreased prolactin level IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20200310 MGI PMID:21368045 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20200310 MGI PMID:21368045 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0005188 small penis IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20200310 MGI PMID:7541529 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20200310 MGI PMID:8046347 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20200310 MGI PMID:8046347 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20200310 MGI PMID:198666 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20200310 MGI PMID:8046347 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0008976 delayed female fertility IAGP N RGD:5509061 20200310 MGI PMID:21368045 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0009007 short estrous cycle IAGP N RGD:5509061 20200310 MGI PMID:21368045 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0009012 short diestrus IAGP N RGD:5509061 20200310 MGI PMID:21368045 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0009015 short proestrus IAGP N RGD:5509061 20200310 MGI PMID:21368045 1553302 Gnrh1 gonadotropin releasing hormone 1 gene MP:0009047 short metestrus IAGP N RGD:5509061 20200310 MGI PMID:21368045 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230601 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0000277 abnormal heart shape IEA N RGD:5509061 20210128 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0001304 cataract IEA N RGD:5509061 20210826 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20231207 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20221215 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1553303 Zc3h11a zinc finger CCCH type containing 11A gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1553304 4933428G20Rik RIKEN cDNA 4933428G20 gene gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1553304 4933428G20Rik RIKEN cDNA 4933428G20 gene gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1553304 4933428G20Rik RIKEN cDNA 4933428G20 gene gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1553306 Tnrc6c trinucleotide repeat containing 6C gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1553306 Tnrc6c trinucleotide repeat containing 6C gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:28811219 1553306 Tnrc6c trinucleotide repeat containing 6C gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:28811219 1553306 Tnrc6c trinucleotide repeat containing 6C gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1553306 Tnrc6c trinucleotide repeat containing 6C gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28811219 1553306 Tnrc6c trinucleotide repeat containing 6C gene MP:0011142 abnormal lung-associated mesenchyme development IAGP N RGD:5509061 20200310 MGI PMID:28811219 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:17588474 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:17588474 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17043238 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:8079170 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000215 absent erythrocytes IAGP N RGD:5509061 20141003 MGI PMID:15867096 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000239 absent common myeloid progenitor cells IAGP N RGD:5509061 20141003 MGI PMID:15867096 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15867096 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:14739214 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:8079170 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:23395001 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:15867096 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:17994017 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:15867096 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17588474 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:17043238 1553307 Spi1 Spi-1 proto-oncogene gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:17043238 1553307 Spi1 Spi-1 proto-oncogene gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17588474 1553307 Spi1 Spi-1 proto-oncogene gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:16163358 1553307 Spi1 Spi-1 proto-oncogene gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:16163358 1553307 Spi1 Spi-1 proto-oncogene gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:15914556 1553307 Spi1 Spi-1 proto-oncogene gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8079170 1553307 Spi1 Spi-1 proto-oncogene gene MP:0001586 abnormal erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17588474 1553307 Spi1 Spi-1 proto-oncogene gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17588474 1553307 Spi1 Spi-1 proto-oncogene gene MP:0001603 failure of myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14739214 1553307 Spi1 Spi-1 proto-oncogene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17043238 1553307 Spi1 Spi-1 proto-oncogene gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17588474 1553307 Spi1 Spi-1 proto-oncogene gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17043238 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10229183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8079170 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8079170 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15657291 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17043238 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:10229183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:15867096 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002415 abnormal neutrophil differentiation IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:15914556 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8079170 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002620 abnormal monocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8079170 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1553307 Spi1 Spi-1 proto-oncogene gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:23395001 1553307 Spi1 Spi-1 proto-oncogene gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16163358 1553307 Spi1 Spi-1 proto-oncogene gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23395001 1553307 Spi1 Spi-1 proto-oncogene gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:15914556 1553307 Spi1 Spi-1 proto-oncogene gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17994017 1553307 Spi1 Spi-1 proto-oncogene gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:17994017 1553307 Spi1 Spi-1 proto-oncogene gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10229183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15867096 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17994017 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005022 abnormal immature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10229183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17994017 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17994017 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10229183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15146183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17588474 1553307 Spi1 Spi-1 proto-oncogene gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8079170 1553307 Spi1 Spi-1 proto-oncogene gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17588474 1553307 Spi1 Spi-1 proto-oncogene gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18354487 1553307 Spi1 Spi-1 proto-oncogene gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:14739214 1553307 Spi1 Spi-1 proto-oncogene gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:15867096 1553307 Spi1 Spi-1 proto-oncogene gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0008169 increased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16311598 1553307 Spi1 Spi-1 proto-oncogene gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:10229183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10229183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23395001 1553307 Spi1 Spi-1 proto-oncogene gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18354487 1553307 Spi1 Spi-1 proto-oncogene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17588474 1553307 Spi1 Spi-1 proto-oncogene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18354487 1553307 Spi1 Spi-1 proto-oncogene gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14739214 1553307 Spi1 Spi-1 proto-oncogene gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15867096 1553307 Spi1 Spi-1 proto-oncogene gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8896458 1553307 Spi1 Spi-1 proto-oncogene gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15914556 1553307 Spi1 Spi-1 proto-oncogene gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10229183 1553307 Spi1 Spi-1 proto-oncogene gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18354487 1553307 Spi1 Spi-1 proto-oncogene gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8079170 1553307 Spi1 Spi-1 proto-oncogene gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553307 Spi1 Spi-1 proto-oncogene gene MP:0011241 abnormal fetal derived definitive erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14739214 1553307 Spi1 Spi-1 proto-oncogene gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23395001 1553310 Whrn whirlin gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:5538400 1553310 Whrn whirlin gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:5538400 1553310 Whrn whirlin gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:6034501 1553310 Whrn whirlin gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:20502675 1553310 Whrn whirlin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14098314 1553310 Whrn whirlin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:5538400 1553310 Whrn whirlin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:6034501 1553310 Whrn whirlin gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:20502675 1553310 Whrn whirlin gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:14098314 1553310 Whrn whirlin gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:14098314 1553310 Whrn whirlin gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:6034501 1553310 Whrn whirlin gene MP:0001394 circling IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:6034501 1553310 Whrn whirlin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160929 MGI PMID:27534441 1553310 Whrn whirlin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:14098314 1553310 Whrn whirlin gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:14098314 1553310 Whrn whirlin gene MP:0001410 head bobbing IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:14098314 1553310 Whrn whirlin gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:14098314 1553310 Whrn whirlin gene MP:0001523 impaired righting response IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:5538400 1553310 Whrn whirlin gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:14098314 1553310 Whrn whirlin gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:6034501 1553310 Whrn whirlin gene MP:0001967 deafness IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20141003 MGI 1553310 Whrn whirlin gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:5538400 1553310 Whrn whirlin gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:6034501 1553310 Whrn whirlin gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:6034501 1553310 Whrn whirlin gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20502675 1553310 Whrn whirlin gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20502675 1553310 Whrn whirlin gene MP:0004362 cochlear hair cell degeneration IEA N RGD:5509061 20111116 MGI 1553310 Whrn whirlin gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12124769 1553310 Whrn whirlin gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12124769 1553310 Whrn whirlin gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20332152 1553310 Whrn whirlin gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12124769 1553310 Whrn whirlin gene MP:0004408 decreased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:20502675 1553310 Whrn whirlin gene MP:0004413 absent cochlear microphonics IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0004416 absent cochlear nerve compound action potential IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0004520 short vestibular hair cell stereocilia IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:12124769 1553310 Whrn whirlin gene MP:0004524 short cochlear hair cell stereocilia IAGP N RGD:5509061 20161020 MGI PMID:18160714 1553310 Whrn whirlin gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:12124769 1553310 Whrn whirlin gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:17326148 1553310 Whrn whirlin gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:20332152 1553310 Whrn whirlin gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20161020 MGI PMID:20502675 1553310 Whrn whirlin gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:17326148 1553310 Whrn whirlin gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:20502675 1553310 Whrn whirlin gene MP:0004531 short outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:20332152 1553310 Whrn whirlin gene MP:0004536 short inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:12124769 1553310 Whrn whirlin gene MP:0004536 short inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:17326148 1553310 Whrn whirlin gene MP:0004536 short inner hair cell stereocilia IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0004580 abnormal cochlear hair bundle transient lateral links morphology IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:20502675 1553310 Whrn whirlin gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:6034501 1553310 Whrn whirlin gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:5538400 1553310 Whrn whirlin gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:6034501 1553310 Whrn whirlin gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:24211856 1553310 Whrn whirlin gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:5538400 1553310 Whrn whirlin gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:6034501 1553310 Whrn whirlin gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:14098314 1553310 Whrn whirlin gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:6034501 1553310 Whrn whirlin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:5538400 1553310 Whrn whirlin gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:20502675 1553310 Whrn whirlin gene MP:0006325 impaired hearing IAGP N RGD:5509061 20160929 MGI PMID:27534441 1553310 Whrn whirlin gene MP:0006325 impaired hearing IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0006383 abnormal cochlear frequency tuning IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0006388 abnormal auditory summating potential IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553310 Whrn whirlin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:24211856 1553310 Whrn whirlin gene MP:0008455 abnormal retina rod cell inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:24211856 1553310 Whrn whirlin gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20502675 1553310 Whrn whirlin gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:20502675 1553310 Whrn whirlin gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:5538400 1553310 Whrn whirlin gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:5538400 1553310 Whrn whirlin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20161020 MGI PMID:27117407 1553313 Ttll9 tubulin tyrosine ligase-like family, member 9 gene MP:0001925 male infertility IAGP N RGD:5509061 20191017 MGI PMID:27257088 1553313 Ttll9 tubulin tyrosine ligase-like family, member 9 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20191017 MGI PMID:27257088 1553313 Ttll9 tubulin tyrosine ligase-like family, member 9 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20191017 MGI PMID:27257088 1553313 Ttll9 tubulin tyrosine ligase-like family, member 9 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20191017 MGI PMID:27257088 1553313 Ttll9 tubulin tyrosine ligase-like family, member 9 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20191017 MGI PMID:27257088 1553313 Ttll9 tubulin tyrosine ligase-like family, member 9 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20191017 MGI PMID:27257088 1553313 Ttll9 tubulin tyrosine ligase-like family, member 9 gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20191017 MGI PMID:27257088 1553313 Ttll9 tubulin tyrosine ligase-like family, member 9 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20191017 MGI PMID:27257088 1553313 Ttll9 tubulin tyrosine ligase-like family, member 9 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20191017 MGI PMID:27257088 1553313 Ttll9 tubulin tyrosine ligase-like family, member 9 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20191017 MGI PMID:27257088 1553313 Ttll9 tubulin tyrosine ligase-like family, member 9 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20191017 MGI PMID:27257088 1553314 Med25 mediator complex subunit 25 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1553314 Med25 mediator complex subunit 25 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1553314 Med25 mediator complex subunit 25 gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20201231 MGI 1553314 Med25 mediator complex subunit 25 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1553314 Med25 mediator complex subunit 25 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1553314 Med25 mediator complex subunit 25 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1553314 Med25 mediator complex subunit 25 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1553314 Med25 mediator complex subunit 25 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553314 Med25 mediator complex subunit 25 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1553315 Tuba4a tubulin, alpha 4A gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20200730 MGI PMID:30760556 1553315 Tuba4a tubulin, alpha 4A gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20200730 MGI PMID:30760556 1553315 Tuba4a tubulin, alpha 4A gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200730 MGI PMID:30760556 1553315 Tuba4a tubulin, alpha 4A gene MP:0003405 abnormal platelet shape IAGP N RGD:5509061 20200730 MGI PMID:30760556 1553315 Tuba4a tubulin, alpha 4A gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20200730 MGI PMID:30760556 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20200310 MGI PMID:8673132 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0000751 myopathy IAGP N RGD:5509061 20200310 MGI PMID:8673132 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20200310 MGI PMID:8673131 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20200310 MGI PMID:9294109 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:11809728 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:8673132 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20200310 MGI PMID:10021468 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0004089 dilated sarcoplasmic reticulum IAGP N RGD:5509061 20200310 MGI PMID:8673132 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20200310 MGI PMID:10021468 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20200310 MGI PMID:8673132 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0004092 absent Z line IAGP N RGD:5509061 20200310 MGI PMID:8673132 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20200310 MGI PMID:15598648 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20200310 MGI PMID:15598648 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0006141 abnormal atrioventricular node conduction IAGP N RGD:5509061 20200310 MGI PMID:10021468 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20200310 MGI PMID:8673132 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20200310 MGI PMID:8673132 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20200310 MGI PMID:10021468 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0010559 heart block IAGP N RGD:5509061 20200310 MGI PMID:10021468 1553318 Dmpk dystrophia myotonica-protein kinase gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:8673132 1553326 Blcap bladder cancer associated protein gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1553326 Blcap bladder cancer associated protein gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20230601 MGI 1553326 Blcap bladder cancer associated protein gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1553329 Mt3 metallothionein 3 gene MP:0000192 abnormal mineral level IAGP N RGD:5509061 20141003 MGI PMID:9006971 1553329 Mt3 metallothionein 3 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:14637104 1553329 Mt3 metallothionein 3 gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:14637104 1553329 Mt3 metallothionein 3 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:14637104 1553329 Mt3 metallothionein 3 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:12388585 1553329 Mt3 metallothionein 3 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12388585 1553329 Mt3 metallothionein 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12388585 1553329 Mt3 metallothionein 3 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9006971 1553329 Mt3 metallothionein 3 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:14637104 1553329 Mt3 metallothionein 3 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:9006971 1553329 Mt3 metallothionein 3 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:12388585 1553334 Skp1 S-phase kinase-associated protein 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20201002 MGI PMID:32232159 1553334 Skp1 S-phase kinase-associated protein 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20201002 MGI PMID:32232159 1553334 Skp1 S-phase kinase-associated protein 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20201002 MGI PMID:32232159 1553334 Skp1 S-phase kinase-associated protein 1 gene MP:0004806 absent germ cells IAGP N RGD:5509061 20201002 MGI PMID:32232159 1553334 Skp1 S-phase kinase-associated protein 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20201002 MGI PMID:32232159 1553334 Skp1 S-phase kinase-associated protein 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20201002 MGI PMID:32232159 1553334 Skp1 S-phase kinase-associated protein 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20201002 MGI PMID:32232159 1553334 Skp1 S-phase kinase-associated protein 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20201002 MGI PMID:32232159 1553334 Skp1 S-phase kinase-associated protein 1 gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20201002 MGI PMID:32232159 1553334 Skp1 S-phase kinase-associated protein 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20201002 MGI PMID:32232159 1553334 Skp1 S-phase kinase-associated protein 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20201002 MGI PMID:32232159 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19339551 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15634774 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15634774 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:15634774 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15634774 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:18466748 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15634774 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19339551 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21123569 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18466748 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0005201 abnormal retina pigment epithelium morphology IEA N RGD:5509061 20180215 MGI 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:18466748 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15634774 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15634774 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:15634774 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:19339551 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:19339551 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0008515 thin retina outer nuclear layer IEA N RGD:5509061 20180215 MGI 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20180215 MGI 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:15634774 1553335 Cngb1 cyclic nucleotide gated channel beta 1 gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:19339551 1553337 Echdc1 enoyl Coenzyme A hydratase domain containing 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20240425 MGI PMID:38417553 1553337 Echdc1 enoyl Coenzyme A hydratase domain containing 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20240425 MGI PMID:38417553 1553337 Echdc1 enoyl Coenzyme A hydratase domain containing 1 gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20240425 MGI PMID:38417553 1553337 Echdc1 enoyl Coenzyme A hydratase domain containing 1 gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20240425 MGI PMID:38417553 1553337 Echdc1 enoyl Coenzyme A hydratase domain containing 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20240425 MGI PMID:38417553 1553340 Pisd phosphatidylserine decarboxylase gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20200310 MGI PMID:16192276 1553340 Pisd phosphatidylserine decarboxylase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:16192276 1553340 Pisd phosphatidylserine decarboxylase gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:16192276 1553340 Pisd phosphatidylserine decarboxylase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200310 MGI PMID:16192276 1553340 Pisd phosphatidylserine decarboxylase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20200310 MGI PMID:16192276 1553340 Pisd phosphatidylserine decarboxylase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16192276 1553340 Pisd phosphatidylserine decarboxylase gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20200310 MGI PMID:16192276 1553341 Slc16a4 solute carrier family 16 (monocarboxylic acid transporters), member 4 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1553343 Trmt1l tRNA methyltransferase 1 like gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17198746 1553343 Trmt1l tRNA methyltransferase 1 like gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17198746 1553343 Trmt1l tRNA methyltransferase 1 like gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:17198746 1553343 Trmt1l tRNA methyltransferase 1 like gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:17198746 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20200310 MGI PMID:28235781 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20200310 MGI PMID:28235781 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200310 MGI PMID:28235781 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210826 MGI 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0002573 behavioral despair IAGP N RGD:5509061 20200310 MGI PMID:28235781 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:28235781 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20200310 MGI PMID:28235781 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20200310 MGI PMID:28235781 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20200310 MGI PMID:28235781 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0010569 papillary muscle hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0011915 increased heart left atrium weight IAGP N RGD:5509061 20231221 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20200310 MGI PMID:28235781 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20210826 MGI 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0020419 decreased cardiac muscle relaxation IAGP N RGD:5509061 20200310 MGI PMID:26304555 1553347 Tnnc1 troponin C, cardiac/slow skeletal gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20231221 MGI PMID:26304555 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200310 MGI 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200310 MGI 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0002064 seizures IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17360554 1553352 Sumf1 sulfatase modifying factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1553353 Ggta1 glycoprotein galactosyltransferase alpha 1, 3 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:15161001 1553353 Ggta1 glycoprotein galactosyltransferase alpha 1, 3 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:16082726 1553353 Ggta1 glycoprotein galactosyltransferase alpha 1, 3 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15161001 1553353 Ggta1 glycoprotein galactosyltransferase alpha 1, 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7545161 1553353 Ggta1 glycoprotein galactosyltransferase alpha 1, 3 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18322191 1553353 Ggta1 glycoprotein galactosyltransferase alpha 1, 3 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16082726 1553353 Ggta1 glycoprotein galactosyltransferase alpha 1, 3 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15161001 1553353 Ggta1 glycoprotein galactosyltransferase alpha 1, 3 gene MP:0004942 abnormal B cell selection IAGP N RGD:5509061 20141003 MGI PMID:18322191 1553353 Ggta1 glycoprotein galactosyltransferase alpha 1, 3 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:15161001 1553353 Ggta1 glycoprotein galactosyltransferase alpha 1, 3 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18322191 1553353 Ggta1 glycoprotein galactosyltransferase alpha 1, 3 gene MP:0010255 cortical cataract IAGP N RGD:5509061 20210722 MGI PMID:8560551 1553353 Ggta1 glycoprotein galactosyltransferase alpha 1, 3 gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15161001 1553355 Rab6b RAB6B, member RAS oncogene family gene MP:0001258 decreased body length IEA N RGD:5509061 20200310 MGI 1553355 Rab6b RAB6B, member RAS oncogene family gene MP:0001262 decreased body weight IEA N RGD:5509061 20200310 MGI 1553355 Rab6b RAB6B, member RAS oncogene family gene MP:0001399 hyperactivity IEA N RGD:5509061 20200310 MGI 1553355 Rab6b RAB6B, member RAS oncogene family gene MP:0001732 postnatal growth retardation IEA N RGD:5509061 20200310 MGI 1553355 Rab6b RAB6B, member RAS oncogene family gene MP:0004924 abnormal behavior IEA N RGD:5509061 20200310 MGI 1553355 Rab6b RAB6B, member RAS oncogene family gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1553355 Rab6b RAB6B, member RAS oncogene family gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200310 MGI 1553355 Rab6b RAB6B, member RAS oncogene family gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1553355 Rab6b RAB6B, member RAS oncogene family gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1553356 Il17b interleukin 17B gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20230914 MGI PMID:36814913 1553356 Il17b interleukin 17B gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20160526 MGI PMID:25888259 1553356 Il17b interleukin 17B gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20160526 MGI PMID:25888259 1553356 Il17b interleukin 17B gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20160526 MGI PMID:25888259 1553356 Il17b interleukin 17B gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20160526 MGI PMID:25888259 1553356 Il17b interleukin 17B gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20230914 MGI PMID:36814913 1553356 Il17b interleukin 17B gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20160526 MGI PMID:25888259 1553356 Il17b interleukin 17B gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20160526 MGI PMID:25888259 1553356 Il17b interleukin 17B gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20160526 MGI PMID:25888259 1553356 Il17b interleukin 17B gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20160526 MGI PMID:25888259 1553356 Il17b interleukin 17B gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20160526 MGI PMID:25888259 1553356 Il17b interleukin 17B gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20160526 MGI PMID:25888259 1553356 Il17b interleukin 17B gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20160526 MGI PMID:25888259 1553356 Il17b interleukin 17B gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20230914 MGI PMID:36814913 1553356 Il17b interleukin 17B gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20160526 MGI PMID:25888259 1553356 Il17b interleukin 17B gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20160526 MGI PMID:25888259 1553356 Il17b interleukin 17B gene MP:0011078 increased macrophage cytokine production IAGP N RGD:5509061 20230914 MGI PMID:36814913 1553357 Or55b10 olfactory receptor family 55 subfamily B member 10 gene MP:0001003 abnormal olfactory receptor morphology IAGP N RGD:5509061 20211021 MGI PMID:31378611 1553357 Or55b10 olfactory receptor family 55 subfamily B member 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19186165 1553357 Or55b10 olfactory receptor family 55 subfamily B member 10 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:19186165 1553357 Or55b10 olfactory receptor family 55 subfamily B member 10 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20211021 MGI PMID:31378611 1553360 Gimap4 GTPase, IMAP family member 4 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:16569770 1553364 Leprot leptin receptor overlapping transcript gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20240801 MGI PMID:38716728 1553364 Leprot leptin receptor overlapping transcript gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20240801 MGI PMID:38716728 1553364 Leprot leptin receptor overlapping transcript gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20240801 MGI PMID:38716728 1553364 Leprot leptin receptor overlapping transcript gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1553364 Leprot leptin receptor overlapping transcript gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20240801 MGI PMID:38716728 1553364 Leprot leptin receptor overlapping transcript gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240801 MGI PMID:38716728 1553364 Leprot leptin receptor overlapping transcript gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20240801 MGI PMID:38716728 1553364 Leprot leptin receptor overlapping transcript gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20170105 MGI 1553364 Leprot leptin receptor overlapping transcript gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1553364 Leprot leptin receptor overlapping transcript gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20170105 MGI 1553364 Leprot leptin receptor overlapping transcript gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20240801 MGI PMID:38716728 1553364 Leprot leptin receptor overlapping transcript gene MP:0011939 increased food intake IEA N RGD:5509061 20210128 MGI 1553364 Leprot leptin receptor overlapping transcript gene MP:0011940 decreased food intake IAGP N RGD:5509061 20240801 MGI PMID:38716728 1553364 Leprot leptin receptor overlapping transcript gene MP:0014434 decreased cytokine level IAGP N RGD:5509061 20240801 MGI PMID:38716728 1553364 Leprot leptin receptor overlapping transcript gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240801 MGI PMID:38716728 1553367 Tbc1d14 TBC1 domain family, member 14 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21118569 1553369 Wdr45b WD repeat domain 45B gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553369 Wdr45b WD repeat domain 45B gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553369 Wdr45b WD repeat domain 45B gene MP:0001405 impaired coordination IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553369 Wdr45b WD repeat domain 45B gene MP:0001513 limb grasping IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553369 Wdr45b WD repeat domain 45B gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553369 Wdr45b WD repeat domain 45B gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200402 MGI 1553369 Wdr45b WD repeat domain 45B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553369 Wdr45b WD repeat domain 45B gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553369 Wdr45b WD repeat domain 45B gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553369 Wdr45b WD repeat domain 45B gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553369 Wdr45b WD repeat domain 45B gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553369 Wdr45b WD repeat domain 45B gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553369 Wdr45b WD repeat domain 45B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1553369 Wdr45b WD repeat domain 45B gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553369 Wdr45b WD repeat domain 45B gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553369 Wdr45b WD repeat domain 45B gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553369 Wdr45b WD repeat domain 45B gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553369 Wdr45b WD repeat domain 45B gene MP:0020365 increased brain iron level IAGP N RGD:5509061 20201231 MGI PMID:33082312 1553373 Klk10 kallikrein related-peptidase 10 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 1553373 Klk10 kallikrein related-peptidase 10 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 1553373 Klk10 kallikrein related-peptidase 10 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20240523 MGI 1553373 Klk10 kallikrein related-peptidase 10 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20240523 MGI 1553373 Klk10 kallikrein related-peptidase 10 gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20240523 MGI 1553373 Klk10 kallikrein related-peptidase 10 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1553373 Klk10 kallikrein related-peptidase 10 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20240523 MGI 1553373 Klk10 kallikrein related-peptidase 10 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20240523 MGI 1553373 Klk10 kallikrein related-peptidase 10 gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20240523 MGI 1553374 Txndc11 thioredoxin domain containing 11 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1553374 Txndc11 thioredoxin domain containing 11 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1553374 Txndc11 thioredoxin domain containing 11 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20220519 MGI 1553374 Txndc11 thioredoxin domain containing 11 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220519 MGI 1553374 Txndc11 thioredoxin domain containing 11 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1553374 Txndc11 thioredoxin domain containing 11 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1553374 Txndc11 thioredoxin domain containing 11 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1553374 Txndc11 thioredoxin domain containing 11 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220519 MGI 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0000745 tremors IEA N RGD:5509061 20170105 MGI 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21115496 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21115496 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21115496 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21115496 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20150430 MGI 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21115496 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21115496 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20151112 MGI PMID:22580896 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:21115496 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20150430 MGI 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:21115496 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150430 MGI 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:21115496 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0005285 decreased unsaturated fatty acids level IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21115496 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20151112 MGI PMID:22580896 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20151112 MGI PMID:22580896 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20151112 MGI PMID:22580896 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20151112 MGI PMID:22580896 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20151112 MGI PMID:22580896 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20151112 MGI PMID:22580896 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20150430 MGI 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20150430 MGI 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20211021 MGI 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0012216 decreased plasmalogen level IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0012230 abnormal sphingolipid level IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20151112 MGI PMID:22580896 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0020355 abnormal Sertoli cell barrier morphology IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553375 Sgms1 sphingomyelin synthase 1 gene MP:0020356 abnormal Sertoli cell barrier function IAGP N RGD:5509061 20190425 MGI PMID:27788151 1553376 Pycard PYD and CARD domain containing gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23219391 1553376 Pycard PYD and CARD domain containing gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23219391 1553376 Pycard PYD and CARD domain containing gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15190255 1553376 Pycard PYD and CARD domain containing gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19501000 1553376 Pycard PYD and CARD domain containing gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16717117 1553376 Pycard PYD and CARD domain containing gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16546100 1553376 Pycard PYD and CARD domain containing gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20457908 1553376 Pycard PYD and CARD domain containing gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:21565393 1553376 Pycard PYD and CARD domain containing gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23090995 1553376 Pycard PYD and CARD domain containing gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:21565393 1553376 Pycard PYD and CARD domain containing gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:16407890 1553376 Pycard PYD and CARD domain containing gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:16546100 1553376 Pycard PYD and CARD domain containing gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:20351692 1553376 Pycard PYD and CARD domain containing gene MP:0008136 enlarged Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:21565393 1553376 Pycard PYD and CARD domain containing gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:21565393 1553376 Pycard PYD and CARD domain containing gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20180920 MGI PMID:29263322 1553376 Pycard PYD and CARD domain containing gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20457908 1553376 Pycard PYD and CARD domain containing gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23090995 1553376 Pycard PYD and CARD domain containing gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20457908 1553376 Pycard PYD and CARD domain containing gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15507117 1553376 Pycard PYD and CARD domain containing gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20180920 MGI PMID:29263322 1553376 Pycard PYD and CARD domain containing gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20180920 MGI PMID:29263322 1553376 Pycard PYD and CARD domain containing gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:16546100 1553376 Pycard PYD and CARD domain containing gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:20351692 1553376 Pycard PYD and CARD domain containing gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:22002608 1553376 Pycard PYD and CARD domain containing gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:16546100 1553376 Pycard PYD and CARD domain containing gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:22002608 1553376 Pycard PYD and CARD domain containing gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:15190255 1553376 Pycard PYD and CARD domain containing gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:16546100 1553376 Pycard PYD and CARD domain containing gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:23090995 1553376 Pycard PYD and CARD domain containing gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:15190255 1553376 Pycard PYD and CARD domain containing gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:15507117 1553376 Pycard PYD and CARD domain containing gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:16407889 1553376 Pycard PYD and CARD domain containing gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:16407890 1553376 Pycard PYD and CARD domain containing gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:16546100 1553376 Pycard PYD and CARD domain containing gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:16547271 1553376 Pycard PYD and CARD domain containing gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20457908 1553376 Pycard PYD and CARD domain containing gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 1553376 Pycard PYD and CARD domain containing gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22002608 1553376 Pycard PYD and CARD domain containing gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:23090995 1553376 Pycard PYD and CARD domain containing gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:15190255 1553376 Pycard PYD and CARD domain containing gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:15507117 1553376 Pycard PYD and CARD domain containing gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:16407890 1553376 Pycard PYD and CARD domain containing gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:16547271 1553376 Pycard PYD and CARD domain containing gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:23090995 1553376 Pycard PYD and CARD domain containing gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:15507117 1553376 Pycard PYD and CARD domain containing gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16546100 1553376 Pycard PYD and CARD domain containing gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:22002608 1553376 Pycard PYD and CARD domain containing gene MP:0008896 increased IgG2c level IAGP N RGD:5509061 20141003 MGI PMID:21565393 1553376 Pycard PYD and CARD domain containing gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20141003 MGI PMID:21565393 1553376 Pycard PYD and CARD domain containing gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:20351692 1553377 Oas2 2'-5' oligoadenylate synthetase 2 gene MP:0001881 abnormal mammary gland physiology IAGP N RGD:5509061 20180517 MGI PMID:29117179 1553377 Oas2 2'-5' oligoadenylate synthetase 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20180517 MGI PMID:29117179 1553377 Oas2 2'-5' oligoadenylate synthetase 2 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20180517 MGI PMID:29117179 1553377 Oas2 2'-5' oligoadenylate synthetase 2 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20180517 MGI PMID:29117179 1553377 Oas2 2'-5' oligoadenylate synthetase 2 gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20180517 MGI PMID:29117179 1553377 Oas2 2'-5' oligoadenylate synthetase 2 gene MP:0010249 lactation failure IAGP N RGD:5509061 20180517 MGI PMID:29117179 1553377 Oas2 2'-5' oligoadenylate synthetase 2 gene MP:0013716 hypolactation IAGP N RGD:5509061 20180517 MGI PMID:29117179 1553379 Sccpdh saccharopine dehydrogenase (putative) gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1553379 Sccpdh saccharopine dehydrogenase (putative) gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1553379 Sccpdh saccharopine dehydrogenase (putative) gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20240523 MGI 1553380 Prdm15 PR domain containing 15 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200430 MGI PMID:31950080 1553380 Prdm15 PR domain containing 15 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200430 MGI PMID:31950080 1553380 Prdm15 PR domain containing 15 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200430 MGI PMID:31950080 1553380 Prdm15 PR domain containing 15 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:31950080 1553380 Prdm15 PR domain containing 15 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20220519 MGI 1553380 Prdm15 PR domain containing 15 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20200430 MGI PMID:31950080 1553380 Prdm15 PR domain containing 15 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200430 MGI PMID:31950080 1553380 Prdm15 PR domain containing 15 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200430 MGI PMID:31950080 1553380 Prdm15 PR domain containing 15 gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20200430 MGI PMID:31950080 1553380 Prdm15 PR domain containing 15 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20200430 MGI PMID:31950080 1553380 Prdm15 PR domain containing 15 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20200430 MGI PMID:31950080 1553380 Prdm15 PR domain containing 15 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20200430 MGI PMID:31950080 1553380 Prdm15 PR domain containing 15 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20220519 MGI 1553380 Prdm15 PR domain containing 15 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200430 MGI PMID:31950080 1553380 Prdm15 PR domain containing 15 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1553380 Prdm15 PR domain containing 15 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20200430 MGI PMID:31950080 1553380 Prdm15 PR domain containing 15 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20200430 MGI PMID:31950080 1553380 Prdm15 PR domain containing 15 gene MP:0020515 abnormal visceral yolk sac endoderm morphology IAGP N RGD:5509061 20200430 MGI PMID:31950080 1553380 Prdm15 PR domain containing 15 gene MP:0030324 abnormal anterior head development IAGP N RGD:5509061 20200430 MGI PMID:31950080 1553383 Pfn4 profilin family, member 4 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20230209 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20230209 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20230209 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20230601 MGI 1553383 Pfn4 profilin family, member 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230209 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20230216 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20230209 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20230216 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0005573 increased pulmonary respiratory rate IEA N RGD:5509061 20201022 MGI 1553383 Pfn4 profilin family, member 4 gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 1553383 Pfn4 profilin family, member 4 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20230216 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20230209 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20230209 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20230216 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20230209 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0009235 small sperm head IAGP N RGD:5509061 20230209 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20230216 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0009325 necrospermia IAGP N RGD:5509061 20230216 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20230209 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20230209 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20230209 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20230216 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20230216 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0012125 decreased bronchoconstrictive response IEA N RGD:5509061 20211021 MGI 1553383 Pfn4 profilin family, member 4 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20230216 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20230216 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0030949 abnormal Golgi vesicle transport IAGP N RGD:5509061 20230216 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20230216 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0031355 abnormal proacrosomal vesicle fusion IAGP N RGD:5509061 20230209 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0031374 abnormal manchette assembly IAGP N RGD:5509061 20230216 MGI PMID:35950913 1553383 Pfn4 profilin family, member 4 gene MP:0031388 absent manchette IAGP N RGD:5509061 20230216 MGI PMID:35950913 1553384 Muc13 mucin 13, epithelial transmembrane gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20211202 MGI PMID:21636645 1553384 Muc13 mucin 13, epithelial transmembrane gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20211202 MGI PMID:21636645 1553384 Muc13 mucin 13, epithelial transmembrane gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20211202 MGI PMID:21636645 1553384 Muc13 mucin 13, epithelial transmembrane gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20211202 MGI PMID:21636645 1553384 Muc13 mucin 13, epithelial transmembrane gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20211202 MGI PMID:21636645 1553384 Muc13 mucin 13, epithelial transmembrane gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20211202 MGI PMID:21636645 1553384 Muc13 mucin 13, epithelial transmembrane gene MP:0005036 diarrhea IAGP N RGD:5509061 20211202 MGI PMID:21636645 1553384 Muc13 mucin 13, epithelial transmembrane gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20211202 MGI PMID:21636645 1553384 Muc13 mucin 13, epithelial transmembrane gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20211202 MGI PMID:21636645 1553384 Muc13 mucin 13, epithelial transmembrane gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20211202 MGI PMID:21636645 1553384 Muc13 mucin 13, epithelial transmembrane gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20211202 MGI PMID:21636645 1553384 Muc13 mucin 13, epithelial transmembrane gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20211202 MGI PMID:21636645 1553384 Muc13 mucin 13, epithelial transmembrane gene MP:0013799 abnormal intestinal goblet cell physiology IAGP N RGD:5509061 20211202 MGI PMID:21636645 1553387 Rtn2 reticulon 2 (Z-band associated protein) gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19720795 1553387 Rtn2 reticulon 2 (Z-band associated protein) gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:19720795 1553389 Clk2 CDC-like kinase 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 1553389 Clk2 CDC-like kinase 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20201022 MGI 1553389 Clk2 CDC-like kinase 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20201022 MGI 1553389 Clk2 CDC-like kinase 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20160324 MGI PMID:24458359 1553389 Clk2 CDC-like kinase 2 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20160324 MGI PMID:24458359 1553389 Clk2 CDC-like kinase 2 gene MP:0010953 abnormal fatty acid oxidation IAGP N RGD:5509061 20160324 MGI PMID:24458359 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0000026 abnormal inner ear morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0000534 abnormal ureter morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0000819 abnormal olfactory bulb morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0000826 abnormal third ventricle morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0001917 intraventricular hemorrhage IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0002947 increased hemangioma incidence IEA N RGD:5509061 20210930 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0004160 retroesophageal right subclavian artery IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0005262 coloboma IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0006054 spinal hemorrhage IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0009493 abnormal cystic duct morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0009688 abnormal spinal cord central canal morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0011380 enlarged brain ventricles IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0011513 abnormal vertebral artery morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0013873 abnormal ductus venosus morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0013968 multiple persisting craniopharyngeal ducts IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0014000 anastomosis between internal carotid artery and basilar artery IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0014019 embryo cyst IEA N RGD:5509061 20170504 MGI 1553390 Rala v-ral simian leukemia viral oncogene A (ras related) gene MP:0014087 retrolental blood IEA N RGD:5509061 20180628 MGI 1553391 Impa2 inositol monophosphatase 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:23205734 1553391 Impa2 inositol monophosphatase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201112 MGI PMID:24554717 1553391 Impa2 inositol monophosphatase 2 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:23205734 1553392 Dek DEK proto-oncogene gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:19223548 1553393 Ajuba ajuba LIM protein gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210128 MGI 1553393 Ajuba ajuba LIM protein gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20201022 MGI 1553393 Ajuba ajuba LIM protein gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20201022 MGI 1553393 Ajuba ajuba LIM protein gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:15728191 1553393 Ajuba ajuba LIM protein gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1553393 Ajuba ajuba LIM protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20230209 MGI PMID:35535434 1553393 Ajuba ajuba LIM protein gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:16862162 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16862162 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16862162 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17404240 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16862162 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17404240 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16862162 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16862162 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20210128 MGI 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16862162 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16862162 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17404240 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17404240 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16862162 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17404240 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16862162 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17404240 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16862162 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1553395 Ube2n ubiquitin-conjugating enzyme E2N gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 1553400 Sfxn5 sideroflexin 5 gene MP:0010052 increased grip strength IEA N RGD:5509061 20231207 MGI 1553400 Sfxn5 sideroflexin 5 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24453213 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24453213 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24453213 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:20170518 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0002791 steatorrhea IAGP N RGD:5509061 20141003 MGI PMID:24453213 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:20170518 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20170518 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0004609 vertebral fusion IEA N RGD:5509061 20170105 MGI 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:24453213 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:24453213 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:24453213 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0009147 abnormal pancreatic acinar cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24453213 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0009164 exocrine pancreas atrophy IAGP N RGD:5509061 20141003 MGI PMID:24453213 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20170518 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0009179 abnormal pancreatic alpha cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20170518 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:24453213 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:24453213 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20170518 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20170518 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:24453213 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0012556 increased cell death IAGP N RGD:5509061 20141003 MGI PMID:24453213 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0013139 moribund IAGP N RGD:5509061 20141003 MGI PMID:24453213 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0013220 increased pancreas apoptosis IAGP N RGD:5509061 20160428 MGI PMID:24453213 1553402 Sel1l sel-1 suppressor of lin-12-like (C. elegans) gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20161013 MGI PMID:20170518 1553404 Zfyve28 zinc finger, FYVE domain containing 28 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1553405 Akap3 A kinase anchor protein 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20220224 MGI PMID:31969357 1553405 Akap3 A kinase anchor protein 3 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220224 MGI PMID:31969357 1553405 Akap3 A kinase anchor protein 3 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220224 MGI PMID:31969357 1553405 Akap3 A kinase anchor protein 3 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220224 MGI PMID:31969357 1553405 Akap3 A kinase anchor protein 3 gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20220224 MGI PMID:31969357 1553405 Akap3 A kinase anchor protein 3 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20220224 MGI PMID:31969357 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0000111 cleft palate IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0001127 small ovary IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0002279 abnormal diaphragm morphology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0002652 thin myocardium IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0003105 abnormal heart atrium morphology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0003641 small lung IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0005477 increased circulating thyroxine level IEA N RGD:5509061 20210128 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0009493 abnormal cystic duct morphology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0009494 abnormal biliary ductule morphology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0010439 abnormal hepatic vein morphology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0010912 herniated liver IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0011513 abnormal vertebral artery morphology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0012303 umbilical vein stenosis IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0013163 absent thyroid gland isthmus IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0013852 abnormal Mullerian duct topology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0013878 abnormal ductus venosus valve topology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0013975 abnormal coronary sinus connection IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20180628 MGI 1553407 Zmynd11 zinc finger, MYND domain containing 11 gene MP:0014021 heterochrony IEA N RGD:5509061 20180628 MGI 1553411 Iqca1 IQ motif containing with AAA domain 1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20240523 MGI 1553411 Iqca1 IQ motif containing with AAA domain 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 1553411 Iqca1 IQ motif containing with AAA domain 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1553411 Iqca1 IQ motif containing with AAA domain 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201022 MGI PMID:32588039 1553411 Iqca1 IQ motif containing with AAA domain 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20240523 MGI 1553411 Iqca1 IQ motif containing with AAA domain 1 gene MP:0010511 shortened PR interval IEA N RGD:5509061 20231207 MGI 1553411 Iqca1 IQ motif containing with AAA domain 1 gene MP:0011954 shortened PQ interval IEA N RGD:5509061 20231207 MGI 1553412 Angptl4 angiopoietin-like 4 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17609370 1553412 Angptl4 angiopoietin-like 4 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:17609370 1553412 Angptl4 angiopoietin-like 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16081640 1553412 Angptl4 angiopoietin-like 4 gene MP:0001333 absent optic nerve IEA N RGD:5509061 20200402 MGI 1553412 Angptl4 angiopoietin-like 4 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17609370 1553412 Angptl4 angiopoietin-like 4 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17609370 1553412 Angptl4 angiopoietin-like 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16081640 1553412 Angptl4 angiopoietin-like 4 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17609370 1553412 Angptl4 angiopoietin-like 4 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16081640 1553412 Angptl4 angiopoietin-like 4 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19318355 1553412 Angptl4 angiopoietin-like 4 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:21832056 1553412 Angptl4 angiopoietin-like 4 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:21832056 1553412 Angptl4 angiopoietin-like 4 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:21832056 1553412 Angptl4 angiopoietin-like 4 gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21832056 1553412 Angptl4 angiopoietin-like 4 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17609370 1553412 Angptl4 angiopoietin-like 4 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16081640 1553412 Angptl4 angiopoietin-like 4 gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:17609370 1553412 Angptl4 angiopoietin-like 4 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17609370 1553412 Angptl4 angiopoietin-like 4 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19318355 1553412 Angptl4 angiopoietin-like 4 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:21832056 1553412 Angptl4 angiopoietin-like 4 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:15505215 1553412 Angptl4 angiopoietin-like 4 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:17609370 1553412 Angptl4 angiopoietin-like 4 gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:21832056 1553412 Angptl4 angiopoietin-like 4 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17609370 1553412 Angptl4 angiopoietin-like 4 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15505215 1553412 Angptl4 angiopoietin-like 4 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21832056 1553412 Angptl4 angiopoietin-like 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16081640 1553412 Angptl4 angiopoietin-like 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21832056 1553412 Angptl4 angiopoietin-like 4 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21832056 1553412 Angptl4 angiopoietin-like 4 gene MP:0011578 increased lipoprotein lipase activity IAGP N RGD:5509061 20141003 MGI PMID:16081640 1553412 Angptl4 angiopoietin-like 4 gene MP:0012080 chylous ascites IAGP N RGD:5509061 20141003 MGI PMID:17609370 1553416 Tram1 translocating chain-associating membrane protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 1553416 Tram1 translocating chain-associating membrane protein 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1553416 Tram1 translocating chain-associating membrane protein 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220811 MGI 1553416 Tram1 translocating chain-associating membrane protein 1 gene MP:0001925 male infertility IEA N RGD:5509061 20220811 MGI 1553416 Tram1 translocating chain-associating membrane protein 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1553416 Tram1 translocating chain-associating membrane protein 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220811 MGI 1553416 Tram1 translocating chain-associating membrane protein 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20230601 MGI 1553416 Tram1 translocating chain-associating membrane protein 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20230601 MGI 1553416 Tram1 translocating chain-associating membrane protein 1 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1553416 Tram1 translocating chain-associating membrane protein 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1553416 Tram1 translocating chain-associating membrane protein 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20210805 MGI PMID:33716172 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20210520 MGI 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20210805 MGI PMID:33716172 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20210805 MGI PMID:33716172 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20210128 MGI 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0005355 enlarged thyroid gland IEA N RGD:5509061 20210520 MGI 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20210805 MGI PMID:33716172 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20210805 MGI PMID:33716172 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553418 Wdhd1 WD repeat and HMG-box DNA binding protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1553420 Prrx1 paired related homeobox 1 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0000023 abnormal ear position IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18198333 1553420 Prrx1 paired related homeobox 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:18198333 1553420 Prrx1 paired related homeobox 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0000448 pointed snout IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0000448 pointed snout IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0000486 abnormal pulmonary trunk morphology IAGP N RGD:5509061 20141003 MGI PMID:10664157 1553420 Prrx1 paired related homeobox 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:18198333 1553420 Prrx1 paired related homeobox 1 gene MP:0000548 long limbs IAGP N RGD:5509061 20141003 MGI PMID:18198333 1553420 Prrx1 paired related homeobox 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0000568 ectopic digits IAGP N RGD:5509061 20141003 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15117820 1553420 Prrx1 paired related homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15117820 1553420 Prrx1 paired related homeobox 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0001341 absent eyelids IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15117820 1553420 Prrx1 paired related homeobox 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15117820 1553420 Prrx1 paired related homeobox 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:10664157 1553420 Prrx1 paired related homeobox 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0003142 anotia IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:18198333 1553420 Prrx1 paired related homeobox 1 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15117820 1553420 Prrx1 paired related homeobox 1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:10664157 1553420 Prrx1 paired related homeobox 1 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:10664157 1553420 Prrx1 paired related homeobox 1 gene MP:0004347 abnormal scapular spine morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0004443 absent supraoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0004455 pterygoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0004458 absent alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0004460 alisphenoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0004479 abnormal oval window morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0004603 absent vertebral arch IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0004679 xiphoid process foramen IAGP N RGD:5509061 20181018 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0004899 absent temporal bone squamous part IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0004899 absent temporal bone squamous part IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0004900 absent zygomatic arch IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0005359 growth retardation of incisors IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0006288 small otic capsule IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0008374 abnormal malleus manubrium morphology IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0008375 short malleus manubrium IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0008381 absent gonial bone IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0008919 fused tarsal bones IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20181101 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0009744 postaxial polydactyly IAGP N RGD:5509061 20181101 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0009898 maxillary shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0009898 maxillary shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0009918 abnormal stylohyoid ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0010324 abnormal malleus processus brevis morphology IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0010464 abnormal aortic arch and aortic arch branch attachment IAGP N RGD:5509061 20141003 MGI PMID:10664157 1553420 Prrx1 paired related homeobox 1 gene MP:0010564 abnormal fetal ductus arteriosus morphology IAGP N RGD:5509061 20141003 MGI PMID:10664157 1553420 Prrx1 paired related homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10664157 1553420 Prrx1 paired related homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15117820 1553420 Prrx1 paired related homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0020823 absent pubic symphysis IAGP N RGD:5509061 20181018 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0030108 abnormal incudostapedial joint morphology IAGP N RGD:5509061 20171005 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0030111 absent temporomandibular joint IAGP N RGD:5509061 20171005 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0030297 outer ear hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0030317 absent maxillary zygomatic process IAGP N RGD:5509061 20171109 MGI PMID:9729491 1553420 Prrx1 paired related homeobox 1 gene MP:0030317 absent maxillary zygomatic process IAGP N RGD:5509061 20171109 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0030406 absent stapes obturator foramen IAGP N RGD:5509061 20171207 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0030407 abnormal stapes crus morpholgy IAGP N RGD:5509061 20171207 MGI PMID:7758948 1553420 Prrx1 paired related homeobox 1 gene MP:0030456 abnormal odontoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0030471 abnormal ameloblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:9876178 1553420 Prrx1 paired related homeobox 1 gene MP:0030862 absent triquetrum IAGP N RGD:5509061 20181101 MGI PMID:9882503 1553420 Prrx1 paired related homeobox 1 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:9729491 1553422 Tmed6 transmembrane p24 trafficking protein 6 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1553422 Tmed6 transmembrane p24 trafficking protein 6 gene MP:0000599 enlarged liver IEA N RGD:5509061 20210520 MGI 1553422 Tmed6 transmembrane p24 trafficking protein 6 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1553422 Tmed6 transmembrane p24 trafficking protein 6 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20200514 MGI 1553422 Tmed6 transmembrane p24 trafficking protein 6 gene MP:0004247 small pancreas IEA N RGD:5509061 20200514 MGI 1553428 Fbxo43 F-box protein 43 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:28723571 1553428 Fbxo43 F-box protein 43 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:28723571 1553428 Fbxo43 F-box protein 43 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:28723571 1553428 Fbxo43 F-box protein 43 gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:28723571 1553428 Fbxo43 F-box protein 43 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:28723571 1553428 Fbxo43 F-box protein 43 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:28723571 1553428 Fbxo43 F-box protein 43 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:28723571 1553428 Fbxo43 F-box protein 43 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20200310 MGI PMID:28723571 1553428 Fbxo43 F-box protein 43 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20200310 MGI PMID:28723571 1553428 Fbxo43 F-box protein 43 gene MP:0009443 parthenogenesis IAGP N RGD:5509061 20200310 MGI PMID:28723571 1553428 Fbxo43 F-box protein 43 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:28723571 1553430 Tmem53 transmembrane protein 53 gene MP:0000547 short limbs IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0001255 decreased body height IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0003109 short femur IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0003840 abnormal coronal suture morphology IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0004635 short metatarsal bones IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0011175 platyspondylia IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0030032 high forehead IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0030278 thick neurocranium IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0030417 craniofacial hyperostosis IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553430 Tmem53 transmembrane protein 53 gene MP:0030469 optic canal stenosis IAGP N RGD:5509061 20220203 MGI PMID:33824347 1553432 Ppp1r3g protein phosphatase 1, regulatory subunit 3G gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200310 MGI PMID:27815211 1553432 Ppp1r3g protein phosphatase 1, regulatory subunit 3G gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200310 MGI PMID:27815211 1553432 Ppp1r3g protein phosphatase 1, regulatory subunit 3G gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20200310 MGI PMID:27815211 1553432 Ppp1r3g protein phosphatase 1, regulatory subunit 3G gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:27815211 1553432 Ppp1r3g protein phosphatase 1, regulatory subunit 3G gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:27815211 1553432 Ppp1r3g protein phosphatase 1, regulatory subunit 3G gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20200310 MGI PMID:27815211 1553432 Ppp1r3g protein phosphatase 1, regulatory subunit 3G gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20200310 MGI PMID:27815211 1553432 Ppp1r3g protein phosphatase 1, regulatory subunit 3G gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:27815211 1553432 Ppp1r3g protein phosphatase 1, regulatory subunit 3G gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20200310 MGI PMID:27815211 1553432 Ppp1r3g protein phosphatase 1, regulatory subunit 3G gene MP:0011939 increased food intake IAGP N RGD:5509061 20200310 MGI PMID:27815211 1553432 Ppp1r3g protein phosphatase 1, regulatory subunit 3G gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20200310 MGI PMID:27815211 1553432 Ppp1r3g protein phosphatase 1, regulatory subunit 3G gene MP:0030994 decreased adipose tissue glycogen level IAGP N RGD:5509061 20200310 MGI PMID:27815211 1553432 Ppp1r3g protein phosphatase 1, regulatory subunit 3G gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:27815211 1553435 Stk35 serine/threonine kinase 35 gene MP:0001127 small ovary IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0001293 anophthalmia IEA N RGD:5509061 20240523 MGI 1553435 Stk35 serine/threonine kinase 35 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1553435 Stk35 serine/threonine kinase 35 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201231 MGI 1553435 Stk35 serine/threonine kinase 35 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230601 MGI 1553435 Stk35 serine/threonine kinase 35 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1553435 Stk35 serine/threonine kinase 35 gene MP:0003099 retina detachment IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1553435 Stk35 serine/threonine kinase 35 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0005261 aniridia IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0005542 cornea vascularization IEA N RGD:5509061 20240523 MGI 1553435 Stk35 serine/threonine kinase 35 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1553435 Stk35 serine/threonine kinase 35 gene MP:0006200 vitreous body deposition IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1553435 Stk35 serine/threonine kinase 35 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553435 Stk35 serine/threonine kinase 35 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:29970477 1553437 Selenot selenoprotein T gene MP:0000774 decreased brain size IEA N RGD:5509061 20231207 MGI 1553437 Selenot selenoprotein T gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20231207 MGI 1553437 Selenot selenoprotein T gene MP:0001147 small testis IEA N RGD:5509061 20231207 MGI 1553437 Selenot selenoprotein T gene MP:0001258 decreased body length IEA N RGD:5509061 20230119 MGI 1553437 Selenot selenoprotein T gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1553437 Selenot selenoprotein T gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20231207 MGI 1553437 Selenot selenoprotein T gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1553437 Selenot selenoprotein T gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20231207 MGI 1553437 Selenot selenoprotein T gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23913443 1553437 Selenot selenoprotein T gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:23913443 1553437 Selenot selenoprotein T gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230119 MGI 1553437 Selenot selenoprotein T gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23913443 1553437 Selenot selenoprotein T gene MP:0005333 decreased heart rate IEA N RGD:5509061 20231207 MGI 1553437 Selenot selenoprotein T gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23913443 1553437 Selenot selenoprotein T gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1553437 Selenot selenoprotein T gene MP:0009167 increased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:23913443 1553437 Selenot selenoprotein T gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:23913443 1553437 Selenot selenoprotein T gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20231207 MGI 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20200310 MGI PMID:16995819 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20200310 MGI PMID:17550335 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20200310 MGI PMID:16995819 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20200310 MGI PMID:17550335 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20200310 MGI PMID:16995819 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:14563650 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:15734843 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20200310 MGI PMID:11457855 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20200310 MGI PMID:11498544 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:12177436 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:12057923 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20200310 MGI PMID:17517963 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20200310 MGI PMID:16973879 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20200310 MGI PMID:19342371 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:12368209 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20200310 MGI PMID:15044451 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:16750274 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:21203469 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20200310 MGI PMID:21203469 1553438 Cav1 caveolin 1, caveolae protein gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:21203469 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:18849439 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20200310 MGI PMID:11457855 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20200310 MGI PMID:11498544 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20200310 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:12759258 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:12660144 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:18178722 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20200310 MGI PMID:16750274 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:16750274 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:16750274 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001407 short stride length IAGP N RGD:5509061 20200310 MGI PMID:16750274 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20200310 MGI PMID:16750274 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:16750274 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20200310 MGI PMID:16973879 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:14563650 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001553 abnormal circulating free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20200310 MGI PMID:11457855 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:12057923 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20200310 MGI PMID:15937515 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20200310 MGI PMID:16501011 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20200310 MGI PMID:17517963 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001853 heart inflammation IAGP N RGD:5509061 20200310 MGI PMID:12057923 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20200310 MGI PMID:12388746 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001885 mammary gland duct hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:12368209 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001885 mammary gland duct hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:15044451 1553438 Cav1 caveolin 1, caveolae protein gene MP:0001921 reduced fertility IAGP N RGD:5509061 20200310 MGI PMID:18849439 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002016 ovary cyst IAGP N RGD:5509061 20200310 MGI PMID:21467199 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:15802273 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:12660144 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20200310 MGI PMID:16750274 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:21203469 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:11498544 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20200310 MGI PMID:18849439 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:16982844 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:16982844 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20200310 MGI PMID:16982927 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:12057923 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002626 increased heart rate IEA N RGD:5509061 20210520 MGI 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20200310 MGI PMID:12057923 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20200310 MGI PMID:12177436 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20200310 MGI PMID:12177436 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20200310 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:12177436 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002833 increased heart weight IAGP N RGD:5509061 20200310 MGI PMID:12057923 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20200310 MGI PMID:18178722 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:17550335 1553438 Cav1 caveolin 1, caveolae protein gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20200310 MGI PMID:17098833 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20200310 MGI PMID:18178722 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20200310 MGI PMID:16995819 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20200310 MGI PMID:12167625 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20200310 MGI PMID:18849439 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:15044451 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:17200204 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200310 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003180 abnormal pulmonary endothelial cell surface IAGP N RGD:5509061 20200310 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20200310 MGI PMID:16603689 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:18849439 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20200310 MGI PMID:21203469 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200310 MGI PMID:21203469 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003416 premature bone ossification IAGP N RGD:5509061 20200310 MGI PMID:17550335 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003426 pulmonary interstitial fibrosis IAGP N RGD:5509061 20200310 MGI PMID:11498544 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20200310 MGI PMID:16750274 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20200310 MGI PMID:12177436 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20200310 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20200310 MGI PMID:16995819 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20200310 MGI PMID:17550335 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20200310 MGI PMID:18849439 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20231109 MGI PMID:12177436 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20200310 MGI PMID:12651616 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20200310 MGI PMID:12177436 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20200310 MGI PMID:15937515 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20200310 MGI PMID:16982927 1553438 Cav1 caveolin 1, caveolae protein gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:16973879 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:23652019 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004149 increased bone strength IAGP N RGD:5509061 20200310 MGI PMID:17550335 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004150 absent caveolae IAGP N RGD:5509061 20200310 MGI PMID:11457855 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004150 absent caveolae IAGP N RGD:5509061 20200310 MGI PMID:11498544 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004150 absent caveolae IAGP N RGD:5509061 20200310 MGI PMID:11689550 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004150 absent caveolae IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004150 absent caveolae IAGP N RGD:5509061 20200310 MGI PMID:12057923 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004150 absent caveolae IAGP N RGD:5509061 20200310 MGI PMID:12177436 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004150 absent caveolae IAGP N RGD:5509061 20200310 MGI PMID:15222744 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004150 absent caveolae IAGP N RGD:5509061 20200310 MGI PMID:15937515 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004150 absent caveolae IAGP N RGD:5509061 20200310 MGI PMID:16995819 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004150 absent caveolae IAGP N RGD:5509061 20200310 MGI PMID:18849439 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004150 absent caveolae IAGP N RGD:5509061 20200310 MGI PMID:23652019 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20200310 MGI PMID:21203469 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20200310 MGI PMID:12759258 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004697 abnormal thyroid follicular cell morphology IAGP N RGD:5509061 20200310 MGI PMID:17202321 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20200310 MGI PMID:15222744 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:21203469 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20200310 MGI PMID:17550335 1553438 Cav1 caveolin 1, caveolae protein gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20200310 MGI PMID:21203469 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:14563650 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:14563650 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:15734843 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20200310 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:12057923 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200310 MGI PMID:12660144 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20200310 MGI PMID:14563650 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005360 urolithiasis IAGP N RGD:5509061 20200310 MGI PMID:12651616 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20200310 MGI PMID:12651616 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20200310 MGI PMID:16973879 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20211021 MGI 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20200310 MGI PMID:11498544 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20200310 MGI PMID:18178722 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:12177436 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20200310 MGI PMID:12057923 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:12167625 1553438 Cav1 caveolin 1, caveolae protein gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:23652019 1553438 Cav1 caveolin 1, caveolae protein gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20200310 MGI PMID:17293479 1553438 Cav1 caveolin 1, caveolae protein gene MP:0006080 brain ischemia IAGP N RGD:5509061 20200310 MGI PMID:21203469 1553438 Cav1 caveolin 1, caveolae protein gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20200310 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20200310 MGI PMID:12388746 1553438 Cav1 caveolin 1, caveolae protein gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20200310 MGI PMID:16995819 1553438 Cav1 caveolin 1, caveolae protein gene MP:0006429 abnormal hyaline cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:16995819 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20200310 MGI PMID:15111495 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20200310 MGI PMID:15734843 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20200310 MGI PMID:16750274 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20200310 MGI PMID:21203469 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20200310 MGI PMID:21203469 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20200310 MGI PMID:11689550 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20200310 MGI PMID:16982844 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20200310 MGI PMID:16982844 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20200310 MGI PMID:16982844 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20200310 MGI PMID:16982844 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20200310 MGI PMID:16982844 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20210218 MGI PMID:16982844 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20200310 MGI PMID:16982927 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0008904 abnormal mammary fat pad morphology IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009082 uterus cyst IAGP N RGD:5509061 20200310 MGI PMID:21467199 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15111495 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20200310 MGI PMID:23652019 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15734843 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009122 decreased white fat cell lipid droplet size IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20200310 MGI PMID:15734843 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009251 enlarged endometrial glands IAGP N RGD:5509061 20200310 MGI PMID:21467199 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20200310 MGI PMID:17550335 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:16973879 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20200310 MGI PMID:15044451 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:12368209 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20200310 MGI PMID:21467199 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:16973879 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:16995819 1553438 Cav1 caveolin 1, caveolae protein gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:16982844 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:16750274 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010111 abnormal renal calcium reabsorption IAGP N RGD:5509061 20200310 MGI PMID:12651616 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:12631721 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:19342371 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010358 abnormal free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20200310 MGI PMID:12057923 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20200310 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20200310 MGI PMID:12177436 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010855 pulmonary hyperemia IAGP N RGD:5509061 20200310 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20200310 MGI PMID:17550335 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:17550335 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010896 decreased lung compliance IAGP N RGD:5509061 20200310 MGI PMID:18849439 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010901 abnormal pulmonary alveolar parenchyma morphology IAGP N RGD:5509061 20200310 MGI PMID:11457855 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010935 increased airway resistance IAGP N RGD:5509061 20200310 MGI PMID:18849439 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20200310 MGI PMID:15734843 1553438 Cav1 caveolin 1, caveolae protein gene MP:0011044 increased lung elastance IAGP N RGD:5509061 20200310 MGI PMID:18849439 1553438 Cav1 caveolin 1, caveolae protein gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20200310 MGI PMID:15734843 1553438 Cav1 caveolin 1, caveolae protein gene MP:0011139 increased lung endothelial cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:11498544 1553438 Cav1 caveolin 1, caveolae protein gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:15044451 1553438 Cav1 caveolin 1, caveolae protein gene MP:0011939 increased food intake IAGP N RGD:5509061 20200310 MGI PMID:11739396 1553438 Cav1 caveolin 1, caveolae protein gene MP:0011939 increased food intake IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20200310 MGI PMID:11457855 1553438 Cav1 caveolin 1, caveolae protein gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20200310 MGI PMID:11498544 1553438 Cav1 caveolin 1, caveolae protein gene MP:0013401 increased endometrial gland number IAGP N RGD:5509061 20200310 MGI PMID:21467199 1553438 Cav1 caveolin 1, caveolae protein gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:12177436 1553438 Cav1 caveolin 1, caveolae protein gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:21203469 1553438 Cav1 caveolin 1, caveolae protein gene MP:0020415 abnormal fibroblast chemotaxis IAGP N RGD:5509061 20200310 MGI PMID:17517963 1553438 Cav1 caveolin 1, caveolae protein gene MP:0020416 decreased fibroblast chemotaxis IAGP N RGD:5509061 20200310 MGI PMID:17517963 1553438 Cav1 caveolin 1, caveolae protein gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:17517963 1553438 Cav1 caveolin 1, caveolae protein gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:12057923 1553438 Cav1 caveolin 1, caveolae protein gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0021159 increased heart right ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:12057923 1553438 Cav1 caveolin 1, caveolae protein gene MP:0021183 increased femoral compact bone area IAGP N RGD:5509061 20220922 MGI PMID:17550335 1553438 Cav1 caveolin 1, caveolae protein gene MP:0030876 abnormal costochondral joint morphology IAGP N RGD:5509061 20200310 MGI PMID:16995819 1553438 Cav1 caveolin 1, caveolae protein gene MP:0030942 abnormal microtubule organizing center morphology IAGP N RGD:5509061 20200310 MGI PMID:17517963 1553438 Cav1 caveolin 1, caveolae protein gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0030974 enhanced gluconeogenesis IAGP N RGD:5509061 20200310 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:12057923 1553438 Cav1 caveolin 1, caveolae protein gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:14690422 1553438 Cav1 caveolin 1, caveolae protein gene MP:0031220 increased circulating CXCL10 level IAGP N RGD:5509061 20210218 MGI PMID:16982844 1553438 Cav1 caveolin 1, caveolae protein gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:22326219 1553438 Cav1 caveolin 1, caveolae protein gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:12057923 1553438 Cav1 caveolin 1, caveolae protein gene MP:0031636 increased heart right ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:12177436 1553439 Fahd1 fumarylacetoacetate hydrolase domain containing 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20200310 MGI PMID:25575590 1553440 Dynlrb1 dynein light chain roadblock-type 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20201029 MGI PMID:32088381 1553440 Dynlrb1 dynein light chain roadblock-type 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20201029 MGI PMID:32088381 1553440 Dynlrb1 dynein light chain roadblock-type 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20201029 MGI PMID:32088381 1553440 Dynlrb1 dynein light chain roadblock-type 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20201029 MGI PMID:32088381 1553440 Dynlrb1 dynein light chain roadblock-type 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20201029 MGI PMID:32088381 1553440 Dynlrb1 dynein light chain roadblock-type 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20201029 MGI PMID:32088381 1553440 Dynlrb1 dynein light chain roadblock-type 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20201029 MGI PMID:32088381 1553440 Dynlrb1 dynein light chain roadblock-type 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1553440 Dynlrb1 dynein light chain roadblock-type 1 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20201029 MGI PMID:32088381 1553440 Dynlrb1 dynein light chain roadblock-type 1 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20201029 MGI PMID:32088381 1553440 Dynlrb1 dynein light chain roadblock-type 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20201029 MGI PMID:32088381 1553440 Dynlrb1 dynein light chain roadblock-type 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553441 Cd6 CD6 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20170309 MGI PMID:27909060 1553441 Cd6 CD6 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20170309 MGI PMID:27909060 1553441 Cd6 CD6 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20170309 MGI PMID:27909060 1553441 Cd6 CD6 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20170309 MGI PMID:27909060 1553441 Cd6 CD6 antigen gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20170309 MGI PMID:27909060 1553441 Cd6 CD6 antigen gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20170309 MGI PMID:27909060 1553441 Cd6 CD6 antigen gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20170309 MGI PMID:27909060 1553441 Cd6 CD6 antigen gene MP:0008169 increased B-1b cell number IAGP N RGD:5509061 20170309 MGI PMID:27909060 1553441 Cd6 CD6 antigen gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20170309 MGI PMID:27909060 1553445 Arf1 ADP-ribosylation factor 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20151217 MGI PMID:25305484 1553446 Atp6v1d ATPase, H+ transporting, lysosomal V1 subunit D gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20211021 MGI 1553446 Atp6v1d ATPase, H+ transporting, lysosomal V1 subunit D gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1553446 Atp6v1d ATPase, H+ transporting, lysosomal V1 subunit D gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20211021 MGI 1553446 Atp6v1d ATPase, H+ transporting, lysosomal V1 subunit D gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20211021 MGI 1553446 Atp6v1d ATPase, H+ transporting, lysosomal V1 subunit D gene MP:0005505 thrombocytosis IEA N RGD:5509061 20200402 MGI 1553446 Atp6v1d ATPase, H+ transporting, lysosomal V1 subunit D gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20170105 MGI 1553446 Atp6v1d ATPase, H+ transporting, lysosomal V1 subunit D gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1553446 Atp6v1d ATPase, H+ transporting, lysosomal V1 subunit D gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1553446 Atp6v1d ATPase, H+ transporting, lysosomal V1 subunit D gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1553447 Gjc3 gap junction protein, gamma 3 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:16481432 1553447 Gjc3 gap junction protein, gamma 3 gene MP:0004597 increased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20141003 MGI PMID:16481432 1553447 Gjc3 gap junction protein, gamma 3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20190502 MGI 1553447 Gjc3 gap junction protein, gamma 3 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:16481432 1553447 Gjc3 gap junction protein, gamma 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16481432 1553448 Sos2 SOS Ras/Rho guanine nucleotide exchange factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10938118 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0001346 abnormal lacrimal gland morphology IAGP N RGD:5509061 20141218 MGI PMID:16473829 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16473829 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:16473829 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0002343 abnormal lymph node cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0002347 abnormal lymph node T cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0002363 abnormal spleen marginal sinus morphology IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15302902 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18451854 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22538615 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0002392 abnormal Peyer's patch T cell area morphology IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23334413 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0002499 chronic inflammation IEA N RGD:5509061 20111116 MGI 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:9825957 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:17474155 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:15302902 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:16473829 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:17474155 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0003452 abnormal parotid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:16473829 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20141218 MGI PMID:16473829 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0003884 decreased macrophage cell number IEA N RGD:5509061 20150702 MGI 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17474155 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:16473829 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0008082 increased single-positive T cell number IEA N RGD:5509061 20150702 MGI 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:10520991 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16473829 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0008879 submandibular gland inflammation IAGP N RGD:5509061 20141204 MGI PMID:16473829 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:16473829 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0010740 abnormal dendritic cell chemotaxis IAGP N RGD:5509061 20150924 MGI PMID:23168837 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0013367 parotid gland inflammation IAGP N RGD:5509061 20141218 MGI PMID:16473829 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0013558 abnormal exocrine gland morphology IAGP N RGD:5509061 20150319 MGI PMID:16473829 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:15302902 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0013649 decreased CD11b-high dendritic cell number IAGP N RGD:5509061 20150924 MGI PMID:23168837 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0013655 decreased CD103-positive CD11b-low dendritic cell number IAGP N RGD:5509061 20150924 MGI PMID:23168837 1553451 Ccr7 C-C motif chemokine receptor 7 gene MP:0014472 impaired B cell migration IAGP N RGD:5509061 20240613 MGI PMID:10520991 1553453 Fcrla Fc receptor-like A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1553453 Fcrla Fc receptor-like A gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1553453 Fcrla Fc receptor-like A gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200310 MGI 1553453 Fcrla Fc receptor-like A gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200310 MGI 1553453 Fcrla Fc receptor-like A gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1553453 Fcrla Fc receptor-like A gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20200310 MGI PMID:20668221 1553453 Fcrla Fc receptor-like A gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200310 MGI 1553453 Fcrla Fc receptor-like A gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1553453 Fcrla Fc receptor-like A gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210520 MGI 1553453 Fcrla Fc receptor-like A gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:20668221 1553453 Fcrla Fc receptor-like A gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1553453 Fcrla Fc receptor-like A gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20220519 MGI 1553454 Cd300lg CD300 molecule like family member G gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20200310 MGI 1553454 Cd300lg CD300 molecule like family member G gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200402 MGI 1553454 Cd300lg CD300 molecule like family member G gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20200310 MGI 1553454 Cd300lg CD300 molecule like family member G gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20211021 MGI 1553454 Cd300lg CD300 molecule like family member G gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1553454 Cd300lg CD300 molecule like family member G gene MP:0011939 increased food intake IEA N RGD:5509061 20210128 MGI 1553458 Cirbp cold inducible RNA binding protein gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20141003 MGI PMID:22711815 1553458 Cirbp cold inducible RNA binding protein gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:22711815 1553458 Cirbp cold inducible RNA binding protein gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:22711815 1553458 Cirbp cold inducible RNA binding protein gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22711815 1553461 Nrros negative regulator of reactive oxygen species gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20210128 MGI 1553461 Nrros negative regulator of reactive oxygen species gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1553461 Nrros negative regulator of reactive oxygen species gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1553461 Nrros negative regulator of reactive oxygen species gene MP:0001406 abnormal gait IEA N RGD:5509061 20200310 MGI 1553461 Nrros negative regulator of reactive oxygen species gene MP:0001513 limb grasping IEA N RGD:5509061 20200310 MGI 1553461 Nrros negative regulator of reactive oxygen species gene MP:0002409 decreased susceptibility to infection IAGP N RGD:5509061 20200310 MGI PMID:24739962 1553461 Nrros negative regulator of reactive oxygen species gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20210128 MGI 1553461 Nrros negative regulator of reactive oxygen species gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:24739962 1553461 Nrros negative regulator of reactive oxygen species gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200310 MGI PMID:24739962 1553461 Nrros negative regulator of reactive oxygen species gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210128 MGI 1553461 Nrros negative regulator of reactive oxygen species gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20200310 MGI PMID:24739962 1553462 Btaf1 B-TFIID TATA-box binding protein associated factor 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20200310 MGI PMID:21419221 1553462 Btaf1 B-TFIID TATA-box binding protein associated factor 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:21419221 1553462 Btaf1 B-TFIID TATA-box binding protein associated factor 1 gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:21419221 1553462 Btaf1 B-TFIID TATA-box binding protein associated factor 1 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20200310 MGI PMID:21419221 1553462 Btaf1 B-TFIID TATA-box binding protein associated factor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:21419221 1553462 Btaf1 B-TFIID TATA-box binding protein associated factor 1 gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:21419221 1553462 Btaf1 B-TFIID TATA-box binding protein associated factor 1 gene MP:0012177 delayed head development IAGP N RGD:5509061 20200310 MGI PMID:21419221 1553464 Papolg poly(A) polymerase gamma gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20210128 MGI 1553464 Papolg poly(A) polymerase gamma gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1553464 Papolg poly(A) polymerase gamma gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20231207 MGI 1553464 Papolg poly(A) polymerase gamma gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1553464 Papolg poly(A) polymerase gamma gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1553469 Rnasel ribonuclease L (2', 5'-oligoisoadenylate synthetase-dependent) gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:9351818 1553469 Rnasel ribonuclease L (2', 5'-oligoisoadenylate synthetase-dependent) gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9351818 1553469 Rnasel ribonuclease L (2', 5'-oligoisoadenylate synthetase-dependent) gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:9351818 1553469 Rnasel ribonuclease L (2', 5'-oligoisoadenylate synthetase-dependent) gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20220616 MGI PMID:34343497 1553469 Rnasel ribonuclease L (2', 5'-oligoisoadenylate synthetase-dependent) gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9351818 1553469 Rnasel ribonuclease L (2', 5'-oligoisoadenylate synthetase-dependent) gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:10366581 1553469 Rnasel ribonuclease L (2', 5'-oligoisoadenylate synthetase-dependent) gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:9351818 1553470 Hcar2 hydroxycarboxylic acid receptor 2 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20200514 MGI 1553470 Hcar2 hydroxycarboxylic acid receptor 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12563315 1553472 Cyp20a1 cytochrome P450, family 20, subfamily a, polypeptide 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1553477 Mid1ip1 Mid1 interacting protein 1 (gastrulation specific G12-like (zebrafish)) gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220519 MGI 1553477 Mid1ip1 Mid1 interacting protein 1 (gastrulation specific G12-like (zebrafish)) gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 1553480 Usp47 ubiquitin specific peptidase 47 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160421 MGI 1553480 Usp47 ubiquitin specific peptidase 47 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1553480 Usp47 ubiquitin specific peptidase 47 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20160421 MGI 1553480 Usp47 ubiquitin specific peptidase 47 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20170105 MGI 1553480 Usp47 ubiquitin specific peptidase 47 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:19966869 1553481 Has3 hyaluronan synthase 3 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:15790861 1553484 Kif27 kinesin family member 27 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21746835 1553484 Kif27 kinesin family member 27 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:21746835 1553484 Kif27 kinesin family member 27 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21746835 1553484 Kif27 kinesin family member 27 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21746835 1553484 Kif27 kinesin family member 27 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21746835 1553484 Kif27 kinesin family member 27 gene MP:0002200 abnormal brain ventricular system morphology IAGP N RGD:5509061 20141003 MGI PMID:21746835 1553484 Kif27 kinesin family member 27 gene MP:0002236 abnormal internal nares morphology IAGP N RGD:5509061 20141003 MGI PMID:21746835 1553484 Kif27 kinesin family member 27 gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20141003 MGI PMID:21746835 1553484 Kif27 kinesin family member 27 gene MP:0030113 maxillary sinus inflammation IAGP N RGD:5509061 20171005 MGI PMID:21746835 1553485 Gk2 glycerol kinase 2 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20190926 MGI PMID:30662012 1553485 Gk2 glycerol kinase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20190926 MGI PMID:28852571 1553485 Gk2 glycerol kinase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20190926 MGI PMID:30662012 1553485 Gk2 glycerol kinase 2 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20190926 MGI PMID:28852571 1553485 Gk2 glycerol kinase 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20190926 MGI PMID:30662012 1553485 Gk2 glycerol kinase 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20190926 MGI PMID:28852571 1553485 Gk2 glycerol kinase 2 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20190926 MGI PMID:28852571 1553485 Gk2 glycerol kinase 2 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20190926 MGI PMID:30662012 1553485 Gk2 glycerol kinase 2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20190926 MGI PMID:28852571 1553485 Gk2 glycerol kinase 2 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20190926 MGI PMID:28852571 1553485 Gk2 glycerol kinase 2 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20190926 MGI PMID:30662012 1553485 Gk2 glycerol kinase 2 gene MP:0014464 decreased sperm mitochondrial sheath size IAGP N RGD:5509061 20240613 MGI PMID:28852571 1553486 Cd300e CD300E molecule gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1553486 Cd300e CD300E molecule gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210520 MGI 1553486 Cd300e CD300E molecule gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210520 MGI 1553486 Cd300e CD300E molecule gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:15860530 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220721 MGI PMID:29411926 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15860530 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17964540 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11114194 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:11114194 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11114194 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24385426 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:20042581 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220721 MGI PMID:29411926 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220721 MGI PMID:29411926 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:17964540 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17964540 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20042581 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11114194 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0004184 abnormal baroreceptor physiology IAGP N RGD:5509061 20141003 MGI PMID:15860530 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220721 MGI PMID:29411926 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:16143109 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17964540 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17964540 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:16143109 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:12522242 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:11114194 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0008454 absent retina rod cells IAGP N RGD:5509061 20141003 MGI PMID:11114194 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:20042581 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20042581 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:11114194 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20042581 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:20042581 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17964540 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17964540 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17964540 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17964540 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0011021 abnormal circadian regulation of heart rate IAGP N RGD:5509061 20141003 MGI PMID:17964540 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0011021 abnormal circadian regulation of heart rate IAGP N RGD:5509061 20171012 MGI PMID:15860530 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0011022 abnormal circadian regulation of systemic arterial blood pressure IAGP N RGD:5509061 20171012 MGI PMID:15860530 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20221215 MGI 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220721 MGI PMID:29411926 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:10217146 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:15860530 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0020468 abnormal circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:10217146 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0020468 abnormal circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:23471982 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:10217146 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:10518585 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:10217146 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:10518585 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:12381662 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:11114194 1553489 Cry1 cryptochrome circadian regulator 1 gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20171012 MGI PMID:11114194 1553490 Celf6 CUGBP, Elav-like family member 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:23407934 1553490 Celf6 CUGBP, Elav-like family member 6 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20200310 MGI PMID:23407934 1553490 Celf6 CUGBP, Elav-like family member 6 gene MP:0003462 abnormal response to novel odor IAGP N RGD:5509061 20200310 MGI PMID:23407934 1553490 Celf6 CUGBP, Elav-like family member 6 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20200310 MGI PMID:23407934 1553490 Celf6 CUGBP, Elav-like family member 6 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20200310 MGI PMID:23407934 1553490 Celf6 CUGBP, Elav-like family member 6 gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20200310 MGI PMID:23407934 1553490 Celf6 CUGBP, Elav-like family member 6 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20200310 MGI PMID:23407934 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0000162 lordosis IEA N RGD:5509061 20210520 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0000599 enlarged liver IEA N RGD:5509061 20210520 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20210520 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0003604 single kidney IEA N RGD:5509061 20210520 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230601 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220519 MGI 1553491 Zc3h8 zinc finger CCCH type containing 8 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20211021 MGI 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20200310 MGI PMID:20333300 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20200310 MGI PMID:17418495 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:21745644 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:21745644 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0001261 obese IAGP N RGD:5509061 20200310 MGI PMID:25157144 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:19160495 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20230921 MGI PMID:37261953 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20200310 MGI PMID:16701208 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20230921 MGI PMID:37261953 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20200310 MGI PMID:21745644 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:16701208 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:20333300 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20200310 MGI PMID:17418495 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20200310 MGI PMID:20333300 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:21745644 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:21745644 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:17418495 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:21745644 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20230921 MGI PMID:37261953 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20230921 MGI PMID:37261953 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0002911 abnormal inhibitory postsynaptic potential IAGP N RGD:5509061 20200310 MGI PMID:17418495 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:16701208 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:19160495 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:21745644 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20210826 MGI PMID:32954490 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20200310 MGI PMID:16701208 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20200310 MGI PMID:17418495 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20200310 MGI PMID:17418495 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20200310 MGI PMID:16701208 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20210826 MGI PMID:32954490 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20200310 MGI PMID:16701208 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:19160495 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20200310 MGI PMID:19160495 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:19160495 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20230921 MGI PMID:37261953 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20200310 MGI PMID:20333300 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20200310 MGI PMID:16701208 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20200310 MGI PMID:20333300 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:21745644 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:19160495 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0010146 umbilical hernia IAGP N RGD:5509061 20200310 MGI PMID:20333300 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20200310 MGI PMID:19160495 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20200310 MGI PMID:17418495 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17418495 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16701208 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20333300 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:37261953 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0020422 decreased freezing behavior IAGP N RGD:5509061 20230921 MGI PMID:37261953 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0020424 increased kindling response IAGP N RGD:5509061 20210826 MGI PMID:32954490 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20230921 MGI PMID:37261953 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0021010 impaired synaptic physiology IAGP N RGD:5509061 20230921 MGI PMID:37261953 1553492 Slc32a1 solute carrier family 32 (GABA vesicular transporter), member 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:19160495 1553493 Cenpj centromere protein J gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0001391 abnormal tail movements IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20200310 MGI PMID:24706806 1553493 Cenpj centromere protein J gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:24706806 1553493 Cenpj centromere protein J gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20200310 MGI PMID:24706806 1553493 Cenpj centromere protein J gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20200310 MGI PMID:24706806 1553493 Cenpj centromere protein J gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:24706806 1553493 Cenpj centromere protein J gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:24706806 1553493 Cenpj centromere protein J gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200310 MGI PMID:24706806 1553493 Cenpj centromere protein J gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20200310 MGI PMID:24706806 1553493 Cenpj centromere protein J gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0004222 iris synechia IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:24706806 1553493 Cenpj centromere protein J gene MP:0004284 abnormal Descemet membrane morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0004373 bowed humerus IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0004609 vertebral fusion IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0004657 small sacral vertebrae IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0004708 short lumbar vertebrae IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0004924 abnormal behavior IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0005015 increased T cell number IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0005108 abnormal ulna morphology IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0005352 small cranium IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0008297 retention of the adrenal gland x-zone IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0009199 abnormal external male genitalia morphology IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200310 MGI 1553493 Cenpj centromere protein J gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23213448 1553493 Cenpj centromere protein J gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24706806 1553493 Cenpj centromere protein J gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:24706806 1553493 Cenpj centromere protein J gene MP:0014164 abnormal ciliary process morphology IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0030048 sloping forehead IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0030167 decreased inner canthal distance IAGP N RGD:5509061 20200310 MGI PMID:23166506 1553493 Cenpj centromere protein J gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20200310 MGI PMID:24706806 1553494 Oxsr1 oxidative-stress responsive 1 gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:21972418 1553494 Oxsr1 oxidative-stress responsive 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:21972418 1553494 Oxsr1 oxidative-stress responsive 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22648948 1553494 Oxsr1 oxidative-stress responsive 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:21972418 1553494 Oxsr1 oxidative-stress responsive 1 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:21972418 1553494 Oxsr1 oxidative-stress responsive 1 gene MP:0005461 abnormal dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22648948 1553494 Oxsr1 oxidative-stress responsive 1 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:21972418 1553494 Oxsr1 oxidative-stress responsive 1 gene MP:0005628 decreased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:21972418 1553494 Oxsr1 oxidative-stress responsive 1 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:21972418 1553494 Oxsr1 oxidative-stress responsive 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20091762 1553494 Oxsr1 oxidative-stress responsive 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19307180 1553494 Oxsr1 oxidative-stress responsive 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20091762 1553496 Rpl7l1 ribosomal protein L7-like 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20200310 MGI 1553496 Rpl7l1 ribosomal protein L7-like 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200310 MGI 1553496 Rpl7l1 ribosomal protein L7-like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553496 Rpl7l1 ribosomal protein L7-like 1 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 1553496 Rpl7l1 ribosomal protein L7-like 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1553497 Adgre1 adhesion G protein-coupled receptor E1 gene MP:0002451 abnormal macrophage physiology IEA N RGD:5509061 20141003 MGI 1553497 Adgre1 adhesion G protein-coupled receptor E1 gene MP:0003884 decreased macrophage cell number IEA N RGD:5509061 20141003 MGI 1553497 Adgre1 adhesion G protein-coupled receptor E1 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15883173 1553497 Adgre1 adhesion G protein-coupled receptor E1 gene MP:0005000 abnormal immune tolerance IAGP N RGD:5509061 20141003 MGI PMID:15883173 1553499 Rnf187 ring finger protein 187 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20240523 MGI 1553499 Rnf187 ring finger protein 187 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1553499 Rnf187 ring finger protein 187 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240627 MGI 1553499 Rnf187 ring finger protein 187 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230601 MGI 1553499 Rnf187 ring finger protein 187 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20240523 MGI 1553499 Rnf187 ring finger protein 187 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210520 MGI 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0010162 increased brain cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553501 Fuca1 fucosidase, alpha-L- 1, tissue gene MP:0011874 enlarged urinary bladder IAGP N RGD:5509061 20200310 MGI PMID:27491075 1553502 Ntf5 neurotrophin 5 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:9973328 1553502 Ntf5 neurotrophin 5 gene MP:0000745 tremors IEA N RGD:5509061 20160421 MGI 1553502 Ntf5 neurotrophin 5 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10681461 1553502 Ntf5 neurotrophin 5 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:10681461 1553502 Ntf5 neurotrophin 5 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:7746324 1553502 Ntf5 neurotrophin 5 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:7746325 1553502 Ntf5 neurotrophin 5 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:10681461 1553502 Ntf5 neurotrophin 5 gene MP:0001021 small L4 dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746325 1553502 Ntf5 neurotrophin 5 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:10681461 1553502 Ntf5 neurotrophin 5 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10995552 1553502 Ntf5 neurotrophin 5 gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746325 1553502 Ntf5 neurotrophin 5 gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746324 1553502 Ntf5 neurotrophin 5 gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746325 1553502 Ntf5 neurotrophin 5 gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746324 1553502 Ntf5 neurotrophin 5 gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746325 1553502 Ntf5 neurotrophin 5 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:10681461 1553502 Ntf5 neurotrophin 5 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746324 1553502 Ntf5 neurotrophin 5 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746325 1553502 Ntf5 neurotrophin 5 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:9973328 1553502 Ntf5 neurotrophin 5 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1553502 Ntf5 neurotrophin 5 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210826 MGI 1553502 Ntf5 neurotrophin 5 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:7746324 1553502 Ntf5 neurotrophin 5 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10681461 1553502 Ntf5 neurotrophin 5 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:7746325 1553502 Ntf5 neurotrophin 5 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:7746324 1553502 Ntf5 neurotrophin 5 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:7746324 1553502 Ntf5 neurotrophin 5 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:7746325 1553502 Ntf5 neurotrophin 5 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160421 MGI 1553502 Ntf5 neurotrophin 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7746324 1553502 Ntf5 neurotrophin 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7746325 1553502 Ntf5 neurotrophin 5 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1553502 Ntf5 neurotrophin 5 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1553502 Ntf5 neurotrophin 5 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10995552 1553502 Ntf5 neurotrophin 5 gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20211021 MGI 1553502 Ntf5 neurotrophin 5 gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:7746325 1553502 Ntf5 neurotrophin 5 gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:8674435 1553502 Ntf5 neurotrophin 5 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1553502 Ntf5 neurotrophin 5 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 1553502 Ntf5 neurotrophin 5 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:10681461 1553502 Ntf5 neurotrophin 5 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20211021 MGI 1553502 Ntf5 neurotrophin 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7746324 1553502 Ntf5 neurotrophin 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7746325 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:17389239 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15071184 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15071184 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:15071184 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15071184 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:15071184 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15071184 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17389239 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15071184 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15071184 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17389239 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20160811 MGI 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0004781 abnormal surfactant composition IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17389239 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:17389239 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0008570 lipidosis IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15071184 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17389239 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0010889 small alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0010891 increased alveolar lamellar body number IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0010998 pulmonary alveolar proteinosis IAGP N RGD:5509061 20141003 MGI PMID:23843985 1553506 Npc2 NPC intracellular cholesterol transporter 2 gene MP:0031632 increased lung cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:23843985 1553508 Atl1 atlastin GTPase 1 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11685207 1553508 Atl1 atlastin GTPase 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0005248 abnormal Harderian gland morphology IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0009517 abnormal salivary gland duct morphology IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0010946 hyperpnea IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0012051 spasticity IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0014320 abnormal autopod rotation IAGP N RGD:5509061 20240404 MGI PMID:11685207 1553508 Atl1 atlastin GTPase 1 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553508 Atl1 atlastin GTPase 1 gene MP:0031204 hindlimb paresis IAGP N RGD:5509061 20230504 MGI PMID:35348668 1553509 Fbxo11 F-box protein 11 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:17035249 1553509 Fbxo11 F-box protein 11 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17035249 1553509 Fbxo11 F-box protein 11 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1553509 Fbxo11 F-box protein 11 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20181227 MGI 1553509 Fbxo11 F-box protein 11 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20170720 MGI PMID:25827072 1553509 Fbxo11 F-box protein 11 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:12943368 1553509 Fbxo11 F-box protein 11 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20170720 MGI PMID:25827072 1553509 Fbxo11 F-box protein 11 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20170720 MGI PMID:25827072 1553509 Fbxo11 F-box protein 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12943368 1553509 Fbxo11 F-box protein 11 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12943368 1553509 Fbxo11 F-box protein 11 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:17035249 1553509 Fbxo11 F-box protein 11 gene MP:0001399 hyperactivity IEA N RGD:5509061 20170105 MGI 1553509 Fbxo11 F-box protein 11 gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20171228 MGI PMID:20057387 1553509 Fbxo11 F-box protein 11 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17035249 1553509 Fbxo11 F-box protein 11 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:12943368 1553509 Fbxo11 F-box protein 11 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:17035249 1553509 Fbxo11 F-box protein 11 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20171228 MGI PMID:20057387 1553509 Fbxo11 F-box protein 11 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:10932191 1553509 Fbxo11 F-box protein 11 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:12943368 1553509 Fbxo11 F-box protein 11 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1553509 Fbxo11 F-box protein 11 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20181227 MGI 1553509 Fbxo11 F-box protein 11 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20181227 MGI 1553509 Fbxo11 F-box protein 11 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:12943368 1553509 Fbxo11 F-box protein 11 gene MP:0003330 abnormal auditory tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12943368 1553509 Fbxo11 F-box protein 11 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20210128 MGI 1553509 Fbxo11 F-box protein 11 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:12943368 1553509 Fbxo11 F-box protein 11 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12943368 1553509 Fbxo11 F-box protein 11 gene MP:0005287 narrow eye opening IEA N RGD:5509061 20240523 MGI 1553509 Fbxo11 F-box protein 11 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 1553509 Fbxo11 F-box protein 11 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:17035249 1553509 Fbxo11 F-box protein 11 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20171228 MGI PMID:20057387 1553509 Fbxo11 F-box protein 11 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:12943368 1553509 Fbxo11 F-box protein 11 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20170720 MGI PMID:25827072 1553509 Fbxo11 F-box protein 11 gene MP:0009603 absent keratohyalin granules IAGP N RGD:5509061 20170720 MGI PMID:25827072 1553509 Fbxo11 F-box protein 11 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210520 MGI 1553509 Fbxo11 F-box protein 11 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17035249 1553509 Fbxo11 F-box protein 11 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170720 MGI PMID:25827072 1553509 Fbxo11 F-box protein 11 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17035249 1553509 Fbxo11 F-box protein 11 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17035249 1553509 Fbxo11 F-box protein 11 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553509 Fbxo11 F-box protein 11 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20221215 MGI 1553509 Fbxo11 F-box protein 11 gene MP:0030066 short face IAGP N RGD:5509061 20170921 MGI PMID:17035249 1553509 Fbxo11 F-box protein 11 gene MP:0030154 abnormal tympanic cavity morphology IAGP N RGD:5509061 20171005 MGI PMID:12943368 1553509 Fbxo11 F-box protein 11 gene MP:0030226 middle ear polyps IAGP N RGD:5509061 20171019 MGI PMID:12943368 1553509 Fbxo11 F-box protein 11 gene MP:0030226 middle ear polyps IAGP N RGD:5509061 20171228 MGI PMID:20057387 1553509 Fbxo11 F-box protein 11 gene MP:0030410 middle ear effusion IAGP N RGD:5509061 20171207 MGI PMID:12943368 1553509 Fbxo11 F-box protein 11 gene MP:0030410 middle ear effusion IAGP N RGD:5509061 20171228 MGI PMID:20057387 1553509 Fbxo11 F-box protein 11 gene MP:0030413 tympanic membrane retraction IAGP N RGD:5509061 20171207 MGI PMID:12943368 1553509 Fbxo11 F-box protein 11 gene MP:0030419 excessive cerumen IAGP N RGD:5509061 20171207 MGI PMID:12943368 1553510 Parp4 poly (ADP-ribose) polymerase family, member 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1553510 Parp4 poly (ADP-ribose) polymerase family, member 4 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1553510 Parp4 poly (ADP-ribose) polymerase family, member 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15169895 1553510 Parp4 poly (ADP-ribose) polymerase family, member 4 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1553510 Parp4 poly (ADP-ribose) polymerase family, member 4 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20220811 MGI 1553510 Parp4 poly (ADP-ribose) polymerase family, member 4 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1553510 Parp4 poly (ADP-ribose) polymerase family, member 4 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1553512 Pwp1 PWP1 homolog, endonuclein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553513 Tlr3 toll-like receptor 3 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:20713712 1553513 Tlr3 toll-like receptor 3 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:20713712 1553513 Tlr3 toll-like receptor 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20713712 1553513 Tlr3 toll-like receptor 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20713712 1553513 Tlr3 toll-like receptor 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:18223009 1553513 Tlr3 toll-like receptor 3 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:16936008 1553513 Tlr3 toll-like receptor 3 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11607032 1553513 Tlr3 toll-like receptor 3 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20233880 1553513 Tlr3 toll-like receptor 3 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:20713712 1553513 Tlr3 toll-like receptor 3 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:16424225 1553513 Tlr3 toll-like receptor 3 gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20200625 MGI PMID:26015500 1553513 Tlr3 toll-like receptor 3 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12960379 1553513 Tlr3 toll-like receptor 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11607032 1553513 Tlr3 toll-like receptor 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:14625548 1553513 Tlr3 toll-like receptor 3 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11607032 1553513 Tlr3 toll-like receptor 3 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:20713712 1553513 Tlr3 toll-like receptor 3 gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20141003 MGI PMID:18032677 1553513 Tlr3 toll-like receptor 3 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:21317384 1553513 Tlr3 toll-like receptor 3 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:14993594 1553513 Tlr3 toll-like receptor 3 gene MP:0003106 abnormal fear-related response IAGP N RGD:5509061 20141003 MGI PMID:20713712 1553513 Tlr3 toll-like receptor 3 gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:20713712 1553513 Tlr3 toll-like receptor 3 gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:20713712 1553513 Tlr3 toll-like receptor 3 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:20713712 1553513 Tlr3 toll-like receptor 3 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18223009 1553513 Tlr3 toll-like receptor 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18032677 1553513 Tlr3 toll-like receptor 3 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:21220319 1553513 Tlr3 toll-like receptor 3 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:19357791 1553513 Tlr3 toll-like receptor 3 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:18032677 1553513 Tlr3 toll-like receptor 3 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:16782847 1553513 Tlr3 toll-like receptor 3 gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14993594 1553513 Tlr3 toll-like receptor 3 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:20713712 1553513 Tlr3 toll-like receptor 3 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:20713712 1553513 Tlr3 toll-like receptor 3 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:20713712 1553513 Tlr3 toll-like receptor 3 gene MP:0008561 decreased tumor necrosis factor secretion IEA N RGD:5509061 20151015 MGI 1553513 Tlr3 toll-like receptor 3 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20200423 MGI PMID:16985170 1553513 Tlr3 toll-like receptor 3 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20180125 MGI PMID:28970238 1553513 Tlr3 toll-like receptor 3 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:16517751 1553513 Tlr3 toll-like receptor 3 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:16936008 1553513 Tlr3 toll-like receptor 3 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:16936008 1553513 Tlr3 toll-like receptor 3 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:16424225 1553513 Tlr3 toll-like receptor 3 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:16936008 1553513 Tlr3 toll-like receptor 3 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16936008 1553513 Tlr3 toll-like receptor 3 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:19357791 1553513 Tlr3 toll-like receptor 3 gene MP:0009167 increased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:19357791 1553513 Tlr3 toll-like receptor 3 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:19239422 1553513 Tlr3 toll-like receptor 3 gene MP:0009669 abnormal postimplantation uterine environment IAGP N RGD:5509061 20141003 MGI PMID:19239422 1553513 Tlr3 toll-like receptor 3 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14993594 1553513 Tlr3 toll-like receptor 3 gene MP:0011079 decreased macrophage cytokine production IEA N RGD:5509061 20151015 MGI 1553513 Tlr3 toll-like receptor 3 gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:18490751 1553513 Tlr3 toll-like receptor 3 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:14993594 1553513 Tlr3 toll-like receptor 3 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200625 MGI PMID:26015500 1553513 Tlr3 toll-like receptor 3 gene MP:0031023 decreased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:18490751 1553513 Tlr3 toll-like receptor 3 gene MP:0031040 increased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:16936008 1553513 Tlr3 toll-like receptor 3 gene MP:0031079 increased circulating troponin I level IAGP N RGD:5509061 20200618 MGI PMID:16936008 1553514 Cpm carboxypeptidase M gene MP:0001262 decreased body weight IEA N RGD:5509061 20231207 MGI 1553514 Cpm carboxypeptidase M gene MP:0005387 immune system phenotype IEA N RGD:5509061 20231207 MGI 1553514 Cpm carboxypeptidase M gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20231207 MGI 1553514 Cpm carboxypeptidase M gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20231207 MGI 1553514 Cpm carboxypeptidase M gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20231207 MGI 1553517 Gnl2 guanine nucleotide binding protein nucleolar 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1553517 Gnl2 guanine nucleotide binding protein nucleolar 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 1553517 Gnl2 guanine nucleotide binding protein nucleolar 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20240523 MGI 1553517 Gnl2 guanine nucleotide binding protein nucleolar 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20240523 MGI 1553517 Gnl2 guanine nucleotide binding protein nucleolar 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20240523 MGI 1553517 Gnl2 guanine nucleotide binding protein nucleolar 2 gene MP:0010895 increased lung compliance IEA N RGD:5509061 20240523 MGI 1553517 Gnl2 guanine nucleotide binding protein nucleolar 2 gene MP:0011045 decreased lung elastance IEA N RGD:5509061 20240523 MGI 1553517 Gnl2 guanine nucleotide binding protein nucleolar 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1553518 Ecm1 extracellular matrix protein 1 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20201022 MGI 1553518 Ecm1 extracellular matrix protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21217760 1553518 Ecm1 extracellular matrix protein 1 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:21217760 1553518 Ecm1 extracellular matrix protein 1 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:21217760 1553518 Ecm1 extracellular matrix protein 1 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:21217760 1553518 Ecm1 extracellular matrix protein 1 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:21217760 1553518 Ecm1 extracellular matrix protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1553520 Ndufv1 NADH:ubiquinone oxidoreductase core subunit V1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1553520 Ndufv1 NADH:ubiquinone oxidoreductase core subunit V1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1553520 Ndufv1 NADH:ubiquinone oxidoreductase core subunit V1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 1553520 Ndufv1 NADH:ubiquinone oxidoreductase core subunit V1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1553520 Ndufv1 NADH:ubiquinone oxidoreductase core subunit V1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553520 Ndufv1 NADH:ubiquinone oxidoreductase core subunit V1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:22144095 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:22144095 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:22773818 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:22144095 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:22144095 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:22144095 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:22144095 1553522 Havcr1 hepatitis A virus cellular receptor 1 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:22144095 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0000015 abnormal ear pigmentation IAGP N RGD:5509061 20200310 MGI PMID:18424845 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20200310 MGI PMID:18424845 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20200310 MGI PMID:18424845 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0005101 abnormal ciliary body pigmentation IAGP N RGD:5509061 20200310 MGI PMID:18424845 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20200310 MGI PMID:18424845 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20200310 MGI PMID:18424845 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:18424845 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20200310 MGI PMID:18424845 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220519 MGI 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0006159 ocular albinism IAGP N RGD:5509061 20200310 MGI PMID:18424845 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:18424845 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0008731 abnormal hair shaft melanin granule morphology IAGP N RGD:5509061 20200310 MGI PMID:18424845 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0009273 abnormal hair shaft melanin granule shape IAGP N RGD:5509061 20200310 MGI PMID:18424845 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0009385 abnormal dermal pigmentation IAGP N RGD:5509061 20200310 MGI PMID:18424845 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0009387 abnormal epidermal pigmentation IAGP N RGD:5509061 20200310 MGI PMID:18424845 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0010052 increased grip strength IEA N RGD:5509061 20200310 MGI 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0012122 abnormal iris transillumination IEA N RGD:5509061 20200310 MGI 1553523 Slc24a5 solute carrier family 24, member 5 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20200310 MGI 1553525 Parp2 poly (ADP-ribose) polymerase family, member 2 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20200310 MGI PMID:12727891 1553525 Parp2 poly (ADP-ribose) polymerase family, member 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:12727891 1553525 Parp2 poly (ADP-ribose) polymerase family, member 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:12727891 1553525 Parp2 poly (ADP-ribose) polymerase family, member 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:12727891 1553525 Parp2 poly (ADP-ribose) polymerase family, member 2 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20200310 MGI PMID:12727891 1553525 Parp2 poly (ADP-ribose) polymerase family, member 2 gene MP:0003701 elevated level of mitotic sister chromatid exchange IAGP N RGD:5509061 20200310 MGI PMID:12727891 1553525 Parp2 poly (ADP-ribose) polymerase family, member 2 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20200310 MGI PMID:12727891 1553525 Parp2 poly (ADP-ribose) polymerase family, member 2 gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20200310 MGI PMID:12727891 1553525 Parp2 poly (ADP-ribose) polymerase family, member 2 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20200310 MGI PMID:12727891 1553525 Parp2 poly (ADP-ribose) polymerase family, member 2 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20200310 MGI PMID:12727891 1553525 Parp2 poly (ADP-ribose) polymerase family, member 2 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20200310 MGI PMID:12727891 1553525 Parp2 poly (ADP-ribose) polymerase family, member 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12727891 1553525 Parp2 poly (ADP-ribose) polymerase family, member 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12727891 1553526 Wdr62 WD repeat domain 62 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:31197141 1553526 Wdr62 WD repeat domain 62 gene MP:0000433 microcephaly IAGP N RGD:5509061 20200310 MGI PMID:24875059 1553526 Wdr62 WD repeat domain 62 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20200310 MGI 1553526 Wdr62 WD repeat domain 62 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:31197141 1553526 Wdr62 WD repeat domain 62 gene MP:0001147 small testis IAGP N RGD:5509061 20210923 MGI PMID:34059773 1553526 Wdr62 WD repeat domain 62 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20200310 MGI 1553526 Wdr62 WD repeat domain 62 gene MP:0001297 microphthalmia IEA N RGD:5509061 20200310 MGI 1553526 Wdr62 WD repeat domain 62 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20200310 MGI PMID:24875059 1553526 Wdr62 WD repeat domain 62 gene MP:0001925 male infertility IAGP N RGD:5509061 20210923 MGI PMID:34059773 1553526 Wdr62 WD repeat domain 62 gene MP:0001926 female infertility IAGP N RGD:5509061 20210923 MGI PMID:34059773 1553526 Wdr62 WD repeat domain 62 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20200310 MGI PMID:31197141 1553526 Wdr62 WD repeat domain 62 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20210923 MGI PMID:34059773 1553526 Wdr62 WD repeat domain 62 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210923 MGI PMID:34059773 1553526 Wdr62 WD repeat domain 62 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210923 MGI PMID:34059773 1553526 Wdr62 WD repeat domain 62 gene MP:0002989 small kidney IEA N RGD:5509061 20200310 MGI 1553526 Wdr62 WD repeat domain 62 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:31197141 1553526 Wdr62 WD repeat domain 62 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20200310 MGI PMID:24875059 1553526 Wdr62 WD repeat domain 62 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20200310 MGI PMID:31197141 1553526 Wdr62 WD repeat domain 62 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20200310 MGI PMID:24875059 1553526 Wdr62 WD repeat domain 62 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200310 MGI PMID:24875059 1553526 Wdr62 WD repeat domain 62 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:24875059 1553526 Wdr62 WD repeat domain 62 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20210923 MGI PMID:34059773 1553526 Wdr62 WD repeat domain 62 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210923 MGI PMID:34059773 1553526 Wdr62 WD repeat domain 62 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20200310 MGI PMID:24875059 1553526 Wdr62 WD repeat domain 62 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20200310 MGI PMID:31197141 1553526 Wdr62 WD repeat domain 62 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20210923 MGI PMID:34059773 1553526 Wdr62 WD repeat domain 62 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210923 MGI PMID:34059773 1553526 Wdr62 WD repeat domain 62 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1553526 Wdr62 WD repeat domain 62 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20200310 MGI PMID:24875059 1553526 Wdr62 WD repeat domain 62 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20210923 MGI PMID:34059773 1553526 Wdr62 WD repeat domain 62 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20210923 MGI PMID:34059773 1553526 Wdr62 WD repeat domain 62 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20210923 MGI PMID:34059773 1553526 Wdr62 WD repeat domain 62 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20200310 MGI PMID:24875059 1553526 Wdr62 WD repeat domain 62 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1553526 Wdr62 WD repeat domain 62 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210923 MGI PMID:34059773 1553526 Wdr62 WD repeat domain 62 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20200310 MGI PMID:24875059 1553526 Wdr62 WD repeat domain 62 gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20200310 MGI PMID:24875059 1553526 Wdr62 WD repeat domain 62 gene MP:0012504 increased forebrain apoptosis IAGP N RGD:5509061 20200310 MGI PMID:31197141 1553526 Wdr62 WD repeat domain 62 gene MP:0012556 increased cell death IAGP N RGD:5509061 20200310 MGI PMID:24875059 1553526 Wdr62 WD repeat domain 62 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20200310 MGI PMID:31197141 1553526 Wdr62 WD repeat domain 62 gene MP:0020066 abnormal neocortex size IAGP N RGD:5509061 20200310 MGI PMID:31197141 1553526 Wdr62 WD repeat domain 62 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210923 MGI PMID:34059773 1553526 Wdr62 WD repeat domain 62 gene MP:0031375 abnormal manchette disassembly IAGP N RGD:5509061 20220407 MGI PMID:34059773 1553528 Masp2 MBL associated serine protease 2 gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:17142762 1553528 Masp2 MBL associated serine protease 2 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:21502512 1553528 Masp2 MBL associated serine protease 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:21502512 1553528 Masp2 MBL associated serine protease 2 gene MP:0009062 impaired lectin complement pathway IAGP N RGD:5509061 20141003 MGI PMID:21502512 1553530 Zfp641 zinc finger protein 641 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1553530 Zfp641 zinc finger protein 641 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20221215 MGI 1553530 Zfp641 zinc finger protein 641 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20221215 MGI 1553530 Zfp641 zinc finger protein 641 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20221215 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12759446 1553531 Rac1 Rac family small GTPase 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12759446 1553531 Rac1 Rac family small GTPase 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231109 MGI PMID:33804107 1553531 Rac1 Rac family small GTPase 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20231109 MGI PMID:33804107 1553531 Rac1 Rac family small GTPase 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20231109 MGI PMID:33804107 1553531 Rac1 Rac family small GTPase 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16651530 1553531 Rac1 Rac family small GTPase 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20231116 MGI PMID:25315346 1553531 Rac1 Rac family small GTPase 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231109 MGI PMID:33804107 1553531 Rac1 Rac family small GTPase 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20231116 MGI PMID:25315346 1553531 Rac1 Rac family small GTPase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21693517 1553531 Rac1 Rac family small GTPase 1 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:16943436 1553531 Rac1 Rac family small GTPase 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16081735 1553531 Rac1 Rac family small GTPase 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16943436 1553531 Rac1 Rac family small GTPase 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16943436 1553531 Rac1 Rac family small GTPase 1 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:16081735 1553531 Rac1 Rac family small GTPase 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:18423204 1553531 Rac1 Rac family small GTPase 1 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:18423204 1553531 Rac1 Rac family small GTPase 1 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:16081735 1553531 Rac1 Rac family small GTPase 1 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:16943436 1553531 Rac1 Rac family small GTPase 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:18702697 1553531 Rac1 Rac family small GTPase 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:18702697 1553531 Rac1 Rac family small GTPase 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:18702697 1553531 Rac1 Rac family small GTPase 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20152175 1553531 Rac1 Rac family small GTPase 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:16943436 1553531 Rac1 Rac family small GTPase 1 gene MP:0001213 abnormal skin cell number IAGP N RGD:5509061 20141003 MGI PMID:16081735 1553531 Rac1 Rac family small GTPase 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16081735 1553531 Rac1 Rac family small GTPase 1 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:16081735 1553531 Rac1 Rac family small GTPase 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20201022 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16651530 1553531 Rac1 Rac family small GTPase 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21693517 1553531 Rac1 Rac family small GTPase 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:21693517 1553531 Rac1 Rac family small GTPase 1 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:10030666 1553531 Rac1 Rac family small GTPase 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:21693517 1553531 Rac1 Rac family small GTPase 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10030666 1553531 Rac1 Rac family small GTPase 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:10030666 1553531 Rac1 Rac family small GTPase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10030666 1553531 Rac1 Rac family small GTPase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21693517 1553531 Rac1 Rac family small GTPase 1 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:21693517 1553531 Rac1 Rac family small GTPase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:20689803 1553531 Rac1 Rac family small GTPase 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14564011 1553531 Rac1 Rac family small GTPase 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:21693517 1553531 Rac1 Rac family small GTPase 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20201022 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16943436 1553531 Rac1 Rac family small GTPase 1 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:18702697 1553531 Rac1 Rac family small GTPase 1 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:20689803 1553531 Rac1 Rac family small GTPase 1 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:21693517 1553531 Rac1 Rac family small GTPase 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:20152175 1553531 Rac1 Rac family small GTPase 1 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16081735 1553531 Rac1 Rac family small GTPase 1 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16943436 1553531 Rac1 Rac family small GTPase 1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:21693517 1553531 Rac1 Rac family small GTPase 1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20231116 MGI PMID:25315346 1553531 Rac1 Rac family small GTPase 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:16651530 1553531 Rac1 Rac family small GTPase 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20180201 MGI PMID:21693517 1553531 Rac1 Rac family small GTPase 1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:16943436 1553531 Rac1 Rac family small GTPase 1 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:10030666 1553531 Rac1 Rac family small GTPase 1 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:10030666 1553531 Rac1 Rac family small GTPase 1 gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:10030666 1553531 Rac1 Rac family small GTPase 1 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:16651530 1553531 Rac1 Rac family small GTPase 1 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20231116 MGI PMID:25315346 1553531 Rac1 Rac family small GTPase 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:20689803 1553531 Rac1 Rac family small GTPase 1 gene MP:0003989 abnormal barrel cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18702697 1553531 Rac1 Rac family small GTPase 1 gene MP:0004032 abnormal interventricular groove morphology IAGP N RGD:5509061 20231116 MGI PMID:25315346 1553531 Rac1 Rac family small GTPase 1 gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20231109 MGI PMID:33804107 1553531 Rac1 Rac family small GTPase 1 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20231109 MGI PMID:33804107 1553531 Rac1 Rac family small GTPase 1 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:21693517 1553531 Rac1 Rac family small GTPase 1 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20231109 MGI PMID:33804107 1553531 Rac1 Rac family small GTPase 1 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:21693517 1553531 Rac1 Rac family small GTPase 1 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:14564011 1553531 Rac1 Rac family small GTPase 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:14564011 1553531 Rac1 Rac family small GTPase 1 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:12759446 1553531 Rac1 Rac family small GTPase 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:20689803 1553531 Rac1 Rac family small GTPase 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16651530 1553531 Rac1 Rac family small GTPase 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:16943436 1553531 Rac1 Rac family small GTPase 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16651530 1553531 Rac1 Rac family small GTPase 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10030666 1553531 Rac1 Rac family small GTPase 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20231116 MGI PMID:25315346 1553531 Rac1 Rac family small GTPase 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231109 MGI PMID:33804107 1553531 Rac1 Rac family small GTPase 1 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20180118 MGI PMID:25079357 1553531 Rac1 Rac family small GTPase 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:10030666 1553531 Rac1 Rac family small GTPase 1 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:14564011 1553531 Rac1 Rac family small GTPase 1 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:14564011 1553531 Rac1 Rac family small GTPase 1 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:14564011 1553531 Rac1 Rac family small GTPase 1 gene MP:0008222 decreased hippocampal commissure size IAGP N RGD:5509061 20141003 MGI PMID:18702697 1553531 Rac1 Rac family small GTPase 1 gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:18702697 1553531 Rac1 Rac family small GTPase 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:18702697 1553531 Rac1 Rac family small GTPase 1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:18702697 1553531 Rac1 Rac family small GTPase 1 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:12759446 1553531 Rac1 Rac family small GTPase 1 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12759446 1553531 Rac1 Rac family small GTPase 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18702697 1553531 Rac1 Rac family small GTPase 1 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20231109 MGI PMID:33804107 1553531 Rac1 Rac family small GTPase 1 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20231116 MGI PMID:25315346 1553531 Rac1 Rac family small GTPase 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20180118 MGI PMID:25079357 1553531 Rac1 Rac family small GTPase 1 gene MP:0009759 abnormal hair follicle bulge morphology IAGP N RGD:5509061 20181129 MGI PMID:16081735 1553531 Rac1 Rac family small GTPase 1 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:21693517 1553531 Rac1 Rac family small GTPase 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:33804107 1553531 Rac1 Rac family small GTPase 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231116 MGI PMID:25315346 1553531 Rac1 Rac family small GTPase 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20231116 MGI PMID:25315346 1553531 Rac1 Rac family small GTPase 1 gene MP:0010498 abnormal interventricular septum muscular part morphology IAGP N RGD:5509061 20231116 MGI PMID:25315346 1553531 Rac1 Rac family small GTPase 1 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20231109 MGI PMID:33804107 1553531 Rac1 Rac family small GTPase 1 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20231116 MGI PMID:25315346 1553531 Rac1 Rac family small GTPase 1 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20231109 MGI PMID:33804107 1553531 Rac1 Rac family small GTPase 1 gene MP:0010682 abnormal hair follicle infundibulum morphology IAGP N RGD:5509061 20181129 MGI PMID:16081735 1553531 Rac1 Rac family small GTPase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18702697 1553531 Rac1 Rac family small GTPase 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:33804107 1553531 Rac1 Rac family small GTPase 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20231116 MGI PMID:25315346 1553531 Rac1 Rac family small GTPase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20689803 1553531 Rac1 Rac family small GTPase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14564011 1553531 Rac1 Rac family small GTPase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20689803 1553531 Rac1 Rac family small GTPase 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20689803 1553531 Rac1 Rac family small GTPase 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12759446 1553531 Rac1 Rac family small GTPase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10030666 1553531 Rac1 Rac family small GTPase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0011190 thick embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:10030666 1553531 Rac1 Rac family small GTPase 1 gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20141003 MGI PMID:20689803 1553531 Rac1 Rac family small GTPase 1 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20231109 MGI PMID:33804107 1553531 Rac1 Rac family small GTPase 1 gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20231116 MGI PMID:25315346 1553531 Rac1 Rac family small GTPase 1 gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:20689803 1553531 Rac1 Rac family small GTPase 1 gene MP:0012515 abnormal heart apex morphology IAGP N RGD:5509061 20231109 MGI PMID:33804107 1553531 Rac1 Rac family small GTPase 1 gene MP:0012515 abnormal heart apex morphology IAGP N RGD:5509061 20231116 MGI PMID:25315346 1553531 Rac1 Rac family small GTPase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1553531 Rac1 Rac family small GTPase 1 gene MP:0013377 abnormal sebocyte number IAGP N RGD:5509061 20141218 MGI PMID:16081735 1553531 Rac1 Rac family small GTPase 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150219 MGI PMID:21693517 1553531 Rac1 Rac family small GTPase 1 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:18423204 1553531 Rac1 Rac family small GTPase 1 gene MP:0020446 increased NAD(P)H oxidase activity IAGP N RGD:5509061 20170914 MGI PMID:16651530 1553531 Rac1 Rac family small GTPase 1 gene MP:0030538 abnormal notochordal plate morphology IAGP N RGD:5509061 20180201 MGI PMID:21693517 1553531 Rac1 Rac family small GTPase 1 gene MP:0030919 absent hair follicle bulb IAGP N RGD:5509061 20181220 MGI PMID:16081735 1553531 Rac1 Rac family small GTPase 1 gene MP:0031526 thin right ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:25315346 1553533 Syde1 synapse defective 1, Rho GTPase, homolog 1 (C. elegans) gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 1553533 Syde1 synapse defective 1, Rho GTPase, homolog 1 (C. elegans) gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20200310 MGI PMID:27917469 1553533 Syde1 synapse defective 1, Rho GTPase, homolog 1 (C. elegans) gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20200310 MGI PMID:27917469 1553533 Syde1 synapse defective 1, Rho GTPase, homolog 1 (C. elegans) gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20240314 MGI 1553533 Syde1 synapse defective 1, Rho GTPase, homolog 1 (C. elegans) gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20200310 MGI PMID:27917469 1553533 Syde1 synapse defective 1, Rho GTPase, homolog 1 (C. elegans) gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20200310 MGI PMID:27917469 1553533 Syde1 synapse defective 1, Rho GTPase, homolog 1 (C. elegans) gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:23791195 1553533 Syde1 synapse defective 1, Rho GTPase, homolog 1 (C. elegans) gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20200310 MGI PMID:23791195 1553533 Syde1 synapse defective 1, Rho GTPase, homolog 1 (C. elegans) gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20200310 MGI PMID:27917469 1553533 Syde1 synapse defective 1, Rho GTPase, homolog 1 (C. elegans) gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20200310 MGI PMID:27917469 1553533 Syde1 synapse defective 1, Rho GTPase, homolog 1 (C. elegans) gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:27917469 1553533 Syde1 synapse defective 1, Rho GTPase, homolog 1 (C. elegans) gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:27917469 1553533 Syde1 synapse defective 1, Rho GTPase, homolog 1 (C. elegans) gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20200310 MGI PMID:27917469 1553533 Syde1 synapse defective 1, Rho GTPase, homolog 1 (C. elegans) gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230601 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:24089213 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:30254094 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20220120 MGI PMID:31875883 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20200310 MGI PMID:24089213 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220120 MGI PMID:31875883 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220120 MGI PMID:31875883 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20200310 MGI PMID:23973919 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:23973919 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:24553140 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:18849965 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:24553140 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20200310 MGI PMID:30254094 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220120 MGI PMID:31875883 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18849966 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20200310 MGI PMID:23973919 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20200310 MGI PMID:24089213 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20231221 MGI PMID:36198790 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20200310 MGI PMID:23973919 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20200310 MGI PMID:23973919 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20200310 MGI PMID:24089213 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20200310 MGI PMID:18849965 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20200310 MGI PMID:30254094 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20231221 MGI PMID:36198790 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20200310 MGI PMID:23973919 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20200310 MGI PMID:23973919 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20200310 MGI PMID:23973919 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20200310 MGI PMID:24553140 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:18849965 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008684 increased interleukin-18 secretion IAGP N RGD:5509061 20200310 MGI PMID:18849965 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20200310 MGI PMID:23973919 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20231221 MGI PMID:36198790 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20200310 MGI PMID:23973919 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20231221 MGI PMID:36198790 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:24089213 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:30254094 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0008923 thoracoschisis IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20200310 MGI PMID:23973919 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20200310 MGI PMID:24089213 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20231221 MGI PMID:36198790 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0010439 abnormal hepatic vein morphology IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0010490 abnormal inferior vena cava valve morphology IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0011078 increased macrophage cytokine production IAGP N RGD:5509061 20200310 MGI PMID:24553140 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18849965 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20231221 MGI PMID:36198790 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20231221 MGI PMID:36198790 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20200310 MGI PMID:23973919 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20231221 MGI PMID:36198790 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0013830 abnormal intrathoracic topology of vagus nerve IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0013936 abnormal thymus topology IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0013970 absent connection between subcutaneous lymph vessels and lymph sac IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20200310 MGI 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20231221 MGI PMID:36198790 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20200310 MGI PMID:18849965 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200310 MGI PMID:18849965 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200310 MGI PMID:18849966 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200310 MGI PMID:22258505 1553543 Atg16l1 autophagy related 16 like 1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200310 MGI PMID:24553140 1553545 Kremen1 kringle containing transmembrane protein 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20200310 MGI PMID:18505822 1553545 Kremen1 kringle containing transmembrane protein 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:18505822 1553545 Kremen1 kringle containing transmembrane protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:18505822 1553545 Kremen1 kringle containing transmembrane protein 1 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20200310 MGI PMID:18505822 1553545 Kremen1 kringle containing transmembrane protein 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20200310 MGI PMID:18505822 1553545 Kremen1 kringle containing transmembrane protein 1 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20200310 MGI PMID:18505822 1553545 Kremen1 kringle containing transmembrane protein 1 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20200310 MGI PMID:18505822 1553545 Kremen1 kringle containing transmembrane protein 1 gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:18505822 1553546 Krt4 keratin 4 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:16858417 1553546 Krt4 keratin 4 gene MP:0000466 esophageal epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9727004 1553546 Krt4 keratin 4 gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9727004 1553546 Krt4 keratin 4 gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9727004 1553546 Krt4 keratin 4 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:16858417 1553546 Krt4 keratin 4 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9727004 1553546 Krt4 keratin 4 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9727004 1553546 Krt4 keratin 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16858417 1553546 Krt4 keratin 4 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9727004 1553546 Krt4 keratin 4 gene MP:0003745 abnormal oral mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:16858417 1553546 Krt4 keratin 4 gene MP:0003751 oral leukoplakia IAGP N RGD:5509061 20141003 MGI PMID:16858417 1553546 Krt4 keratin 4 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9727004 1553546 Krt4 keratin 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16858417 1553546 Krt4 keratin 4 gene MP:0020854 increased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:9727004 1553546 Krt4 keratin 4 gene MP:0020857 cornea epithelium hyperplasia IAGP N RGD:5509061 20181101 MGI PMID:9727004 1553549 Tiprl TIP41, TOR signalling pathway regulator-like (S. cerevisiae) gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20201231 MGI 1553549 Tiprl TIP41, TOR signalling pathway regulator-like (S. cerevisiae) gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20200310 MGI 1553549 Tiprl TIP41, TOR signalling pathway regulator-like (S. cerevisiae) gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1553549 Tiprl TIP41, TOR signalling pathway regulator-like (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553549 Tiprl TIP41, TOR signalling pathway regulator-like (S. cerevisiae) gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1553549 Tiprl TIP41, TOR signalling pathway regulator-like (S. cerevisiae) gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210826 MGI 1553551 Casr calcium-sensing receptor gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20200310 MGI PMID:11517179 1553551 Casr calcium-sensing receptor gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20200310 MGI PMID:22527485 1553551 Casr calcium-sensing receptor gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20200310 MGI PMID:15347804 1553551 Casr calcium-sensing receptor gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20200310 MGI PMID:11517179 1553551 Casr calcium-sensing receptor gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20200310 MGI PMID:22527485 1553551 Casr calcium-sensing receptor gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20221103 MGI 1553551 Casr calcium-sensing receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:11517179 1553551 Casr calcium-sensing receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:11517179 1553551 Casr calcium-sensing receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:22527485 1553551 Casr calcium-sensing receptor gene MP:0001304 cataract IAGP N RGD:5509061 20200310 MGI PMID:15347804 1553551 Casr calcium-sensing receptor gene MP:0001429 dehydration IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0001438 aphagia IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0001504 abnormal posture IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20200310 MGI PMID:15347804 1553551 Casr calcium-sensing receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1553551 Casr calcium-sensing receptor gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20221103 MGI 1553551 Casr calcium-sensing receptor gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20200310 MGI PMID:22527485 1553551 Casr calcium-sensing receptor gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:15347804 1553551 Casr calcium-sensing receptor gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:11517179 1553551 Casr calcium-sensing receptor gene MP:0002902 decreased urine phosphate level IAGP N RGD:5509061 20200310 MGI PMID:15347804 1553551 Casr calcium-sensing receptor gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20200310 MGI PMID:15347804 1553551 Casr calcium-sensing receptor gene MP:0002980 abnormal postural reflex IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20200310 MGI PMID:15347804 1553551 Casr calcium-sensing receptor gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0003112 enlarged parathyroid gland IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0003114 pigmented parathyroid gland IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0003116 rickets IAGP N RGD:5509061 20200310 MGI PMID:11517179 1553551 Casr calcium-sensing receptor gene MP:0003195 calcinosis IAGP N RGD:5509061 20200310 MGI PMID:15347804 1553551 Casr calcium-sensing receptor gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20200310 MGI PMID:15347804 1553551 Casr calcium-sensing receptor gene MP:0003199 calcified muscle IAGP N RGD:5509061 20200310 MGI PMID:15347804 1553551 Casr calcium-sensing receptor gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20200310 MGI PMID:11517179 1553551 Casr calcium-sensing receptor gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0003493 parathyroid gland hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:22094462 1553551 Casr calcium-sensing receptor gene MP:0004906 enlarged uterus IEA N RGD:5509061 20221103 MGI 1553551 Casr calcium-sensing receptor gene MP:0005202 lethargy IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:22094462 1553551 Casr calcium-sensing receptor gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1553551 Casr calcium-sensing receptor gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0010092 increased circulating magnesium level IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0010965 decreased compact bone volume IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11517179 1553551 Casr calcium-sensing receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20221103 MGI 1553551 Casr calcium-sensing receptor gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0013572 abnormal parathyroid gland chief cell morphology IAGP N RGD:5509061 20200310 MGI PMID:7493018 1553551 Casr calcium-sensing receptor gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:18765830 1553551 Casr calcium-sensing receptor gene MP:0030129 tongue inflammation IAGP N RGD:5509061 20200310 MGI PMID:15347804 1553554 Cd274 CD274 antigen gene MP:0001790 abnormal immune system physiology IEA N RGD:5509061 20200310 MGI 1553554 Cd274 CD274 antigen gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20200310 MGI PMID:25964334 1553554 Cd274 CD274 antigen gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20200310 MGI PMID:15030776 1553554 Cd274 CD274 antigen gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20200310 MGI PMID:16606670 1553554 Cd274 CD274 antigen gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20200310 MGI PMID:19710456 1553554 Cd274 CD274 antigen gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:20639491 1553554 Cd274 CD274 antigen gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15249675 1553554 Cd274 CD274 antigen gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20200310 MGI PMID:20051242 1553554 Cd274 CD274 antigen gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200310 MGI PMID:16358363 1553554 Cd274 CD274 antigen gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200310 MGI PMID:17182110 1553554 Cd274 CD274 antigen gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20200310 MGI PMID:21061440 1553554 Cd274 CD274 antigen gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:15030776 1553554 Cd274 CD274 antigen gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200310 MGI PMID:17182110 1553554 Cd274 CD274 antigen gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200310 MGI PMID:18825752 1553554 Cd274 CD274 antigen gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20200310 MGI PMID:16606670 1553554 Cd274 CD274 antigen gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20200310 MGI PMID:17911591 1553554 Cd274 CD274 antigen gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:21061440 1553554 Cd274 CD274 antigen gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15249675 1553554 Cd274 CD274 antigen gene MP:0005015 increased T cell number IAGP N RGD:5509061 20200310 MGI PMID:18825752 1553554 Cd274 CD274 antigen gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20200310 MGI PMID:16358363 1553554 Cd274 CD274 antigen gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20200310 MGI PMID:20051242 1553554 Cd274 CD274 antigen gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21061440 1553554 Cd274 CD274 antigen gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20200310 MGI PMID:15030776 1553554 Cd274 CD274 antigen gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:15030776 1553554 Cd274 CD274 antigen gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:18490751 1553554 Cd274 CD274 antigen gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18490751 1553554 Cd274 CD274 antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:15030776 1553554 Cd274 CD274 antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:19710456 1553554 Cd274 CD274 antigen gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:17182110 1553554 Cd274 CD274 antigen gene MP:0008087 decreased T helper 1 cell number IAGP N RGD:5509061 20200310 MGI PMID:20639491 1553554 Cd274 CD274 antigen gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:20639491 1553554 Cd274 CD274 antigen gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20200310 MGI PMID:21061440 1553554 Cd274 CD274 antigen gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20200310 MGI PMID:21061440 1553554 Cd274 CD274 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:21061440 1553554 Cd274 CD274 antigen gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:21061440 1553554 Cd274 CD274 antigen gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:20639491 1553554 Cd274 CD274 antigen gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20200310 MGI PMID:20051242 1553554 Cd274 CD274 antigen gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:16606670 1553554 Cd274 CD274 antigen gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:21061440 1553554 Cd274 CD274 antigen gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20200310 MGI PMID:16606670 1553554 Cd274 CD274 antigen gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20200310 MGI PMID:21061440 1553554 Cd274 CD274 antigen gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20200310 MGI PMID:16606670 1553554 Cd274 CD274 antigen gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20200310 MGI PMID:21061440 1553554 Cd274 CD274 antigen gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20200310 MGI PMID:16606670 1553554 Cd274 CD274 antigen gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20200310 MGI PMID:20051242 1553554 Cd274 CD274 antigen gene MP:0008896 increased IgG2c level IAGP N RGD:5509061 20200310 MGI PMID:20639491 1553554 Cd274 CD274 antigen gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:20639491 1553554 Cd274 CD274 antigen gene MP:0010189 abnormal T follicular helper cell physiology IAGP N RGD:5509061 20200310 MGI PMID:21061440 1553554 Cd274 CD274 antigen gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20200310 MGI PMID:21061440 1553554 Cd274 CD274 antigen gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16027236 1553554 Cd274 CD274 antigen gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:18490751 1553554 Cd274 CD274 antigen gene MP:0031023 decreased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:18490751 1553557 Sbk1 SH3-binding kinase 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200402 MGI 1553557 Sbk1 SH3-binding kinase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1553557 Sbk1 SH3-binding kinase 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20201231 MGI 1553557 Sbk1 SH3-binding kinase 1 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 1553557 Sbk1 SH3-binding kinase 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1553559 Plcd1 phospholipase C, delta 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:22805570 1553559 Plcd1 phospholipase C, delta 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20200310 MGI PMID:22805570 1553559 Plcd1 phospholipase C, delta 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:12805213 1553559 Plcd1 phospholipase C, delta 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20200310 MGI PMID:12805213 1553559 Plcd1 phospholipase C, delta 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20200310 MGI PMID:19002527 1553559 Plcd1 phospholipase C, delta 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:22805570 1553559 Plcd1 phospholipase C, delta 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:22805570 1553559 Plcd1 phospholipase C, delta 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:19002527 1553559 Plcd1 phospholipase C, delta 1 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:12805213 1553559 Plcd1 phospholipase C, delta 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:12805213 1553559 Plcd1 phospholipase C, delta 1 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20200310 MGI PMID:12805213 1553559 Plcd1 phospholipase C, delta 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:22805570 1553559 Plcd1 phospholipase C, delta 1 gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20200310 MGI PMID:12805213 1553559 Plcd1 phospholipase C, delta 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:22805570 1553559 Plcd1 phospholipase C, delta 1 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20200310 MGI PMID:22805570 1553559 Plcd1 phospholipase C, delta 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20200310 MGI PMID:22805570 1553559 Plcd1 phospholipase C, delta 1 gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20200310 MGI PMID:22805570 1553559 Plcd1 phospholipase C, delta 1 gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20200310 MGI PMID:22805570 1553559 Plcd1 phospholipase C, delta 1 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20200310 MGI PMID:22805570 1553559 Plcd1 phospholipase C, delta 1 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20200310 MGI PMID:22805570 1553559 Plcd1 phospholipase C, delta 1 gene MP:0009623 enlarged inguinal lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:22805570 1553559 Plcd1 phospholipase C, delta 1 gene MP:0009631 enlarged axillary lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:22805570 1553559 Plcd1 phospholipase C, delta 1 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:12805213 1553559 Plcd1 phospholipase C, delta 1 gene MP:0013378 increased sebocyte number IAGP N RGD:5509061 20200310 MGI PMID:12805213 1553560 Tmprss11b transmembrane protease, serine 11B gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20191031 MGI PMID:31501243 1553561 Dhrs2 dehydrogenase/reductase member 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160421 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20240523 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20210902 MGI PMID:33560420 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0000745 tremors IEA N RGD:5509061 20201231 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20210902 MGI PMID:33560420 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20210902 MGI PMID:33560420 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0001261 obese IAGP N RGD:5509061 20210902 MGI PMID:33560420 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210902 MGI PMID:33560420 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0001924 infertility IAGP N RGD:5509061 20210902 MGI PMID:33560420 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20210902 MGI PMID:33560420 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20210128 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0002764 short tibia IEA N RGD:5509061 20201022 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20210128 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20160421 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20160421 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201022 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160421 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20210902 MGI PMID:33560420 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20210826 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20160421 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20160421 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20210902 MGI PMID:33560420 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20210902 MGI PMID:33560420 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20210128 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20210902 MGI PMID:33560420 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20210902 MGI PMID:33560420 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20160421 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20210902 MGI PMID:33560420 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20201022 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160421 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20210128 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210902 MGI PMID:33560420 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20210902 MGI PMID:33560420 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20191128 MGI PMID:31479441 1553562 Bbs5 Bardet-Biedl syndrome 5 gene MP:0020511 decreased dendritic spine length IAGP N RGD:5509061 20191128 MGI PMID:31479441 1553568 St3gal6 ST3 beta-galactoside alpha-2,3-sialyltransferase 6 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22700726 1553568 St3gal6 ST3 beta-galactoside alpha-2,3-sialyltransferase 6 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22700726 1553568 St3gal6 ST3 beta-galactoside alpha-2,3-sialyltransferase 6 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:22700726 1553568 St3gal6 ST3 beta-galactoside alpha-2,3-sialyltransferase 6 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:22700726 1553568 St3gal6 ST3 beta-galactoside alpha-2,3-sialyltransferase 6 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:22700726 1553568 St3gal6 ST3 beta-galactoside alpha-2,3-sialyltransferase 6 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22700726 1553568 St3gal6 ST3 beta-galactoside alpha-2,3-sialyltransferase 6 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:22700726 1553568 St3gal6 ST3 beta-galactoside alpha-2,3-sialyltransferase 6 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:22700726 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:22922412 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20151112 MGI 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16368758 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:22922412 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:21383102 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16368758 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:21383102 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16368758 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0002829 abnormal juxtaglomerular apparatus morphology IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:22922412 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:22922412 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:22922412 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20141003 MGI PMID:22922412 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:16368758 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0004142 abnormal muscle tone IAGP N RGD:5509061 20141003 MGI PMID:22922412 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16361444 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0005582 increased renin activity IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:22922412 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0005634 decreased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22922412 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:21383102 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:16368758 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0010109 abnormal renal sodium reabsorption IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0010128 hypovolemia IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0011299 abnormal macula densa morphology IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0011300 abnormal juxtaglomerular cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0011302 abnormal extraglomerular mesangial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0011442 abnormal renal sodium ion transport IAGP N RGD:5509061 20141003 MGI PMID:9689096 1553569 Nr3c2 nuclear receptor subfamily 3, group C, member 2 gene MP:0031232 increased circulating angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:9689096 1553572 Tmprss11d transmembrane protease, serine 11d gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20200310 MGI PMID:31501243 1553572 Tmprss11d transmembrane protease, serine 11d gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21853097 1553576 F11r F11 receptor gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15343392 1553576 F11r F11 receptor gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16809549 1553576 F11r F11 receptor gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:15343392 1553576 F11r F11 receptor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16809549 1553577 Gsto2 glutathione S-transferase omega 2 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20201022 MGI 1553577 Gsto2 glutathione S-transferase omega 2 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20200402 MGI 1553577 Gsto2 glutathione S-transferase omega 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20150108 MGI 1553577 Gsto2 glutathione S-transferase omega 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1553585 Plxnd1 plexin D1 gene MP:0000111 cleft palate IEA N RGD:5509061 20141003 MGI 1553585 Plxnd1 plexin D1 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1553585 Plxnd1 plexin D1 gene MP:0000445 short snout IEA N RGD:5509061 20150827 MGI 1553585 Plxnd1 plexin D1 gene MP:0000520 absent kidney IEA N RGD:5509061 20141003 MGI 1553585 Plxnd1 plexin D1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19421194 1553585 Plxnd1 plexin D1 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:19421194 1553585 Plxnd1 plexin D1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20141003 MGI 1553585 Plxnd1 plexin D1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 1553585 Plxnd1 plexin D1 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0002639 micrognathia IEA N RGD:5509061 20150827 MGI 1553585 Plxnd1 plexin D1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0002726 abnormal pulmonary vein morphology IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:24210822 1553585 Plxnd1 plexin D1 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0004612 fusion of vertebral bodies IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20141003 MGI 1553585 Plxnd1 plexin D1 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:21505259 1553585 Plxnd1 plexin D1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0010406 common atrium IEA N RGD:5509061 20150827 MGI 1553585 Plxnd1 plexin D1 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1553585 Plxnd1 plexin D1 gene MP:0010413 complete atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1553585 Plxnd1 plexin D1 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0010466 vascular ring IEA N RGD:5509061 20150827 MGI 1553585 Plxnd1 plexin D1 gene MP:0010472 abnormal ascending aorta and coronary artery attachment IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0010488 abnormal left subclavian artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0010565 absent fetal ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0011661 persistent truncus arteriosus type i IEA N RGD:5509061 20141003 MGI 1553585 Plxnd1 plexin D1 gene MP:0011662 persistent truncus arteriosus type ii IEA N RGD:5509061 20141003 MGI 1553585 Plxnd1 plexin D1 gene MP:0011681 atrium cyst IEA N RGD:5509061 20141003 MGI 1553585 Plxnd1 plexin D1 gene MP:0011682 renal glomerulus cyst IEA N RGD:5509061 20141003 MGI 1553585 Plxnd1 plexin D1 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20141003 MGI 1553585 Plxnd1 plexin D1 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15239958 1553585 Plxnd1 plexin D1 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15550623 1553585 Plxnd1 plexin D1 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18992737 1553585 Plxnd1 plexin D1 gene MP:0013975 abnormal coronary sinus connection IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0020330 increased capillary density IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0031152 subcutaneous hemorrhage IAGP N RGD:5509061 20231109 MGI PMID:34791216 1553585 Plxnd1 plexin D1 gene MP:0031589 detached epicardium IAGP N RGD:5509061 20240229 MGI PMID:18992737 1553588 Notch4 notch 4 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10837027 1553588 Notch4 notch 4 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:10837027 1553588 Notch4 notch 4 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10837027 1553588 Notch4 notch 4 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:10837027 1553588 Notch4 notch 4 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:10837027 1553588 Notch4 notch 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10837027 1553588 Notch4 notch 4 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:10837027 1553588 Notch4 notch 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21991352 1553588 Notch4 notch 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:10837027 1553588 Notch4 notch 4 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:10837027 1553588 Notch4 notch 4 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20160922 MGI PMID:24667410 1553588 Notch4 notch 4 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:10837027 1553588 Notch4 notch 4 gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:10837027 1553588 Notch4 notch 4 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:10837027 1553588 Notch4 notch 4 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10837027 1553588 Notch4 notch 4 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20160922 MGI PMID:24667410 1553588 Notch4 notch 4 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10837027 1553592 Zfp516 zinc finger protein 516 gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20200310 MGI PMID:25578880 1553592 Zfp516 zinc finger protein 516 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20200310 MGI PMID:25578880 1553592 Zfp516 zinc finger protein 516 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25578880 1553592 Zfp516 zinc finger protein 516 gene MP:0011170 abnormal brown fat cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:25578880 1553592 Zfp516 zinc finger protein 516 gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20200310 MGI PMID:25578880 1553593 Otp orthopedia homeobox gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553593 Otp orthopedia homeobox gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553593 Otp orthopedia homeobox gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:11071765 1553593 Otp orthopedia homeobox gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11071765 1553593 Otp orthopedia homeobox gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:11071765 1553593 Otp orthopedia homeobox gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:11071765 1553593 Otp orthopedia homeobox gene MP:0001257 increased body length IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553593 Otp orthopedia homeobox gene MP:0001261 obese IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553593 Otp orthopedia homeobox gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11071765 1553593 Otp orthopedia homeobox gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553593 Otp orthopedia homeobox gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11071765 1553593 Otp orthopedia homeobox gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553593 Otp orthopedia homeobox gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17481897 1553593 Otp orthopedia homeobox gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553593 Otp orthopedia homeobox gene MP:0004164 abnormal neurohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:11071765 1553593 Otp orthopedia homeobox gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553593 Otp orthopedia homeobox gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553593 Otp orthopedia homeobox gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553593 Otp orthopedia homeobox gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553593 Otp orthopedia homeobox gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553593 Otp orthopedia homeobox gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20141003 MGI PMID:11071765 1553593 Otp orthopedia homeobox gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553593 Otp orthopedia homeobox gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1553593 Otp orthopedia homeobox gene MP:0008845 abnormal paraventricular hypothalamic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11071765 1553593 Otp orthopedia homeobox gene MP:0008846 abnormal supraoptic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11071765 1553593 Otp orthopedia homeobox gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20231207 MGI 1553593 Otp orthopedia homeobox gene MP:0009229 abnormal neurohypophysis median eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:11071765 1553593 Otp orthopedia homeobox gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11071765 1553593 Otp orthopedia homeobox gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553593 Otp orthopedia homeobox gene MP:0011939 increased food intake IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553593 Otp orthopedia homeobox gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20200416 MGI PMID:29107289 1553595 Tcf3 transcription factor 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20170314 MGI PMID:26301816 1553595 Tcf3 transcription factor 3 gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:16365147 1553595 Tcf3 transcription factor 3 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:16365147 1553595 Tcf3 transcription factor 3 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16365147 1553595 Tcf3 transcription factor 3 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:16315099 1553595 Tcf3 transcription factor 3 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20170314 MGI PMID:26301816 1553595 Tcf3 transcription factor 3 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:9584174 1553595 Tcf3 transcription factor 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170314 MGI PMID:26301816 1553595 Tcf3 transcription factor 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20170314 MGI PMID:26301816 1553595 Tcf3 transcription factor 3 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:9372963 1553595 Tcf3 transcription factor 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21857655 1553595 Tcf3 transcription factor 3 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8001124 1553595 Tcf3 transcription factor 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16315099 1553595 Tcf3 transcription factor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19822014 1553595 Tcf3 transcription factor 3 gene MP:0001577 anemia IAGP N RGD:5509061 20170314 MGI PMID:26301816 1553595 Tcf3 transcription factor 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19822014 1553595 Tcf3 transcription factor 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8001124 1553595 Tcf3 transcription factor 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8649400 1553595 Tcf3 transcription factor 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9372963 1553595 Tcf3 transcription factor 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9584174 1553595 Tcf3 transcription factor 3 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19752184 1553595 Tcf3 transcription factor 3 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19822014 1553595 Tcf3 transcription factor 3 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9372963 1553595 Tcf3 transcription factor 3 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20170314 MGI PMID:26301816 1553595 Tcf3 transcription factor 3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17442955 1553595 Tcf3 transcription factor 3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18384878 1553595 Tcf3 transcription factor 3 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:16315099 1553595 Tcf3 transcription factor 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9584174 1553595 Tcf3 transcription factor 3 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:20062079 1553595 Tcf3 transcription factor 3 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9372963 1553595 Tcf3 transcription factor 3 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9584174 1553595 Tcf3 transcription factor 3 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:20062079 1553595 Tcf3 transcription factor 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9584174 1553595 Tcf3 transcription factor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19822014 1553595 Tcf3 transcription factor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20062079 1553595 Tcf3 transcription factor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9372963 1553595 Tcf3 transcription factor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9584174 1553595 Tcf3 transcription factor 3 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18538592 1553595 Tcf3 transcription factor 3 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19752184 1553595 Tcf3 transcription factor 3 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20062079 1553595 Tcf3 transcription factor 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11937548 1553595 Tcf3 transcription factor 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16315099 1553595 Tcf3 transcription factor 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18093538 1553595 Tcf3 transcription factor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11937548 1553595 Tcf3 transcription factor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17316599 1553595 Tcf3 transcription factor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22354994 1553595 Tcf3 transcription factor 3 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17452521 1553595 Tcf3 transcription factor 3 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:9584174 1553595 Tcf3 transcription factor 3 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16365147 1553595 Tcf3 transcription factor 3 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:8001125 1553595 Tcf3 transcription factor 3 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:15078898 1553595 Tcf3 transcription factor 3 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:8001124 1553595 Tcf3 transcription factor 3 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20170314 MGI PMID:26301816 1553595 Tcf3 transcription factor 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:16315099 1553595 Tcf3 transcription factor 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:16315099 1553595 Tcf3 transcription factor 3 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20170314 MGI PMID:26301816 1553595 Tcf3 transcription factor 3 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:8001124 1553595 Tcf3 transcription factor 3 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:16315099 1553595 Tcf3 transcription factor 3 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:8001125 1553595 Tcf3 transcription factor 3 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9584174 1553595 Tcf3 transcription factor 3 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18093538 1553595 Tcf3 transcription factor 3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18195039 1553595 Tcf3 transcription factor 3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20062079 1553595 Tcf3 transcription factor 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8001125 1553595 Tcf3 transcription factor 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9372963 1553595 Tcf3 transcription factor 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17452521 1553595 Tcf3 transcription factor 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18538592 1553595 Tcf3 transcription factor 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8001124 1553595 Tcf3 transcription factor 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8001125 1553595 Tcf3 transcription factor 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9584174 1553595 Tcf3 transcription factor 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170314 MGI PMID:26301816 1553595 Tcf3 transcription factor 3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442955 1553595 Tcf3 transcription factor 3 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:20062079 1553595 Tcf3 transcription factor 3 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:11937548 1553595 Tcf3 transcription factor 3 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442955 1553595 Tcf3 transcription factor 3 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:18384878 1553595 Tcf3 transcription factor 3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442955 1553595 Tcf3 transcription factor 3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18384878 1553595 Tcf3 transcription factor 3 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18195039 1553595 Tcf3 transcription factor 3 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17442955 1553595 Tcf3 transcription factor 3 gene MP:0005432 abnormal pro-B cell morphology IAGP N RGD:5509061 20170314 MGI PMID:26301816 1553595 Tcf3 transcription factor 3 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:17452521 1553595 Tcf3 transcription factor 3 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:16365147 1553595 Tcf3 transcription factor 3 gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:19752184 1553595 Tcf3 transcription factor 3 gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:9372963 1553595 Tcf3 transcription factor 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18093538 1553595 Tcf3 transcription factor 3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18093538 1553595 Tcf3 transcription factor 3 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11937548 1553595 Tcf3 transcription factor 3 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18384878 1553595 Tcf3 transcription factor 3 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:16365147 1553595 Tcf3 transcription factor 3 gene MP:0008176 abnormal germinal center B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18538592 1553595 Tcf3 transcription factor 3 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:18538592 1553595 Tcf3 transcription factor 3 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18538592 1553595 Tcf3 transcription factor 3 gene MP:0008187 absent pro-B cells IAGP N RGD:5509061 20141003 MGI PMID:16365147 1553595 Tcf3 transcription factor 3 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18538592 1553595 Tcf3 transcription factor 3 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18538592 1553595 Tcf3 transcription factor 3 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:19752184 1553595 Tcf3 transcription factor 3 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:8649400 1553595 Tcf3 transcription factor 3 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:9584174 1553595 Tcf3 transcription factor 3 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15078898 1553595 Tcf3 transcription factor 3 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18538592 1553595 Tcf3 transcription factor 3 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:19752184 1553595 Tcf3 transcription factor 3 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:9584174 1553595 Tcf3 transcription factor 3 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18538592 1553595 Tcf3 transcription factor 3 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18538592 1553595 Tcf3 transcription factor 3 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20170314 MGI PMID:26301816 1553595 Tcf3 transcription factor 3 gene MP:0008233 abnormal pro-B cell differentiation IAGP N RGD:5509061 20170314 MGI PMID:26301816 1553595 Tcf3 transcription factor 3 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:9372963 1553595 Tcf3 transcription factor 3 gene MP:0008755 abnormal immunoglobulin V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:8001125 1553595 Tcf3 transcription factor 3 gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:18538592 1553595 Tcf3 transcription factor 3 gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:19822014 1553595 Tcf3 transcription factor 3 gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:8001125 1553595 Tcf3 transcription factor 3 gene MP:0008761 abnormal immunoglobulin light chain V-J recombination IAGP N RGD:5509061 20141003 MGI PMID:19752184 1553595 Tcf3 transcription factor 3 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:9372963 1553595 Tcf3 transcription factor 3 gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17452521 1553595 Tcf3 transcription factor 3 gene MP:0009628 absent brachial lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17452521 1553595 Tcf3 transcription factor 3 gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17452521 1553595 Tcf3 transcription factor 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20062079 1553595 Tcf3 transcription factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16315099 1553595 Tcf3 transcription factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8001124 1553595 Tcf3 transcription factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8001125 1553595 Tcf3 transcription factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8649400 1553595 Tcf3 transcription factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9372963 1553595 Tcf3 transcription factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9584174 1553595 Tcf3 transcription factor 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9372963 1553595 Tcf3 transcription factor 3 gene MP:0014050 increased B cell acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20170314 MGI PMID:26301816 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:9314549 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18563383 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18563383 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:9736651 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:18563383 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:11559824 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0001844 autoimmune response IAGP N RGD:5509061 20180111 MGI PMID:21964024 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:8164737 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:9736651 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:24658838 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12093877 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12093877 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12093877 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12093877 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18563383 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12093877 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002083 premature death IAGP N RGD:5509061 20180111 MGI PMID:21964024 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19084435 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002343 abnormal lymph node cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:8164737 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9820556 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17562770 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:8164737 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:9820556 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11559824 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18563383 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:9314549 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:12093877 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:10639149 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:17919943 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0003865 lymph node inflammation IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:9736651 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:9314549 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10946317 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:9314549 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:9736651 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:12594834 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11801676 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:24658838 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:7972104 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:8164737 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:7526382 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:7972104 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:8164737 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:18563383 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18563383 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15308121 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005580 periinsulitis IAGP N RGD:5509061 20141003 MGI PMID:9314549 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20231207 MGI 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:15308121 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:17114464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:9736651 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17919943 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:18563383 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:18563383 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:14557749 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:11559824 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11559824 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008573 increased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:17562770 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008791 decreased NK cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9314549 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0009022 abnormal brain meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15061770 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16116214 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17919943 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0009791 increased susceptibility to viral infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:12093877 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:12093877 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16116214 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17919943 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20141003 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18563383 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0012330 decreased circulating fibrinogen level IAGP N RGD:5509061 20200618 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12093877 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:11559824 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:23160464 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:7526382 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:8164737 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0020916 increased susceptibility to Herpesvirales infection IEA N RGD:5509061 20200430 MGI 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:9736651 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0020943 increased susceptibility to Flaviviridae infection IAGP N RGD:5509061 20200430 MGI PMID:15061770 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:15069016 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IEA N RGD:5509061 20200514 MGI 1553597 Prf1 perforin 1 (pore forming protein) gene MP:0031052 lymph node necrosis IAGP N RGD:5509061 20200618 MGI PMID:15069016 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20240523 MGI 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:16630838 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16630838 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111215 MGI 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0002330 abnormal bronchial provocation IAGP N RGD:5509061 20141003 MGI PMID:19059884 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:16564016 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20141003 MGI PMID:16564016 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:16564016 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0003043 hypoalgesia IEA N RGD:5509061 20111215 MGI 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20181011 MGI PMID:29795268 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:16564016 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0003663 abnormal thermosensation IAGP N RGD:5509061 20141003 MGI PMID:16630838 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220811 MGI 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18499726 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19059884 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0005407 hyperalgesia IAGP N RGD:5509061 20141003 MGI PMID:16564016 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:16630838 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:16564016 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19059884 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0010055 abnormal sensory neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18499726 1553598 Trpa1 transient receptor potential cation channel, subfamily A, member 1 gene MP:0011968 decreased threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16630838 1553600 Colec12 collectin sub-family member 12 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1553600 Colec12 collectin sub-family member 12 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20200514 MGI 1553600 Colec12 collectin sub-family member 12 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200514 MGI 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20201022 MGI 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20181227 MGI 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20221006 MGI PMID:32938917 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0000445 short snout IAGP N RGD:5509061 20221006 MGI PMID:32938917 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0000493 rectal prolapse IEA N RGD:5509061 20240208 MGI 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0000745 tremors IAGP N RGD:5509061 20240222 MGI PMID:38198538 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20240222 MGI PMID:38198538 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20240229 MGI PMID:38198538 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20240222 MGI PMID:38198538 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20221006 MGI PMID:32938917 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20221006 MGI PMID:32938917 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20221006 MGI PMID:32938917 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20240222 MGI PMID:38198538 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20221006 MGI PMID:32938917 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20221006 MGI PMID:32938917 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20221006 MGI PMID:32938917 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20181227 MGI 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20181227 MGI 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20221006 MGI PMID:32938917 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20221006 MGI PMID:32938917 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20221006 MGI PMID:32938917 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20201022 MGI 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:32938917 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0030166 increased inner canthal distance IAGP N RGD:5509061 20221006 MGI PMID:32938917 1553608 Rreb1 ras responsive element binding protein 1 gene MP:0030189 broad snout IAGP N RGD:5509061 20221006 MGI PMID:32938917 1553609 Fgf13 fibroblast growth factor 13 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20210819 MGI PMID:34184986 1553609 Fgf13 fibroblast growth factor 13 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0001499 abnormal kindling response IAGP N RGD:5509061 20160204 MGI PMID:26063919 1553609 Fgf13 fibroblast growth factor 13 gene MP:0002064 seizures IAGP N RGD:5509061 20160204 MGI PMID:26063919 1553609 Fgf13 fibroblast growth factor 13 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20210819 MGI PMID:34184986 1553609 Fgf13 fibroblast growth factor 13 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20160204 MGI PMID:26063919 1553609 Fgf13 fibroblast growth factor 13 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20160204 MGI PMID:26063919 1553609 Fgf13 fibroblast growth factor 13 gene MP:0003063 increased coping response IAGP N RGD:5509061 20210819 MGI PMID:34184986 1553609 Fgf13 fibroblast growth factor 13 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20210819 MGI PMID:34184986 1553609 Fgf13 fibroblast growth factor 13 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20210819 MGI PMID:34184986 1553609 Fgf13 fibroblast growth factor 13 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20210819 MGI PMID:34184986 1553609 Fgf13 fibroblast growth factor 13 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20160204 MGI PMID:26063919 1553609 Fgf13 fibroblast growth factor 13 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20210819 MGI PMID:34184986 1553609 Fgf13 fibroblast growth factor 13 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20210819 MGI PMID:34184986 1553609 Fgf13 fibroblast growth factor 13 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20210819 MGI PMID:34184986 1553609 Fgf13 fibroblast growth factor 13 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22726441 1553609 Fgf13 fibroblast growth factor 13 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160204 MGI PMID:26063919 1553609 Fgf13 fibroblast growth factor 13 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20210819 MGI PMID:34184986 1553609 Fgf13 fibroblast growth factor 13 gene MP:0014378 increased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:26063919 1553609 Fgf13 fibroblast growth factor 13 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:26063919 1553609 Fgf13 fibroblast growth factor 13 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20210819 MGI PMID:34184986 1553611 Ngb neuroglobin gene MP:0020475 delayed circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:22496809 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15140899 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:15140899 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15140899 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15140899 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15140899 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:15140899 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0009974 decreased cerebral cortex pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0010012 ectopic cerebral cortex pyramidal cells IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17682066 1553612 St8sia2 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:17682066 1553613 Psmd6 proteasome (prosome, macropain) 26S subunit, non-ATPase, 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553616 Hcrtr2 hypocretin (orexin) receptor 2 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12797957 1553616 Hcrtr2 hypocretin (orexin) receptor 2 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:21377495 1553616 Hcrtr2 hypocretin (orexin) receptor 2 gene MP:0004142 abnormal muscle tone IAGP N RGD:5509061 20141003 MGI PMID:21368172 1553616 Hcrtr2 hypocretin (orexin) receptor 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21368172 1553616 Hcrtr2 hypocretin (orexin) receptor 2 gene MP:0005279 narcolepsy IAGP N RGD:5509061 20141003 MGI PMID:12797957 1553616 Hcrtr2 hypocretin (orexin) receptor 2 gene MP:0005279 narcolepsy IAGP N RGD:5509061 20141003 MGI PMID:21368172 1553616 Hcrtr2 hypocretin (orexin) receptor 2 gene MP:0009436 fragmentation of sleep/wake states IAGP N RGD:5509061 20141003 MGI PMID:21368172 1553616 Hcrtr2 hypocretin (orexin) receptor 2 gene MP:0012288 abnormal paradoxical sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12797957 1553616 Hcrtr2 hypocretin (orexin) receptor 2 gene MP:0012289 abnormal non-rapid eye movement sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12797957 1553619 Ppp3cc protein phosphatase 3, catalytic subunit, gamma isoform gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20160818 MGI PMID:26429887 1553619 Ppp3cc protein phosphatase 3, catalytic subunit, gamma isoform gene MP:0001925 male infertility IAGP N RGD:5509061 20160818 MGI PMID:26429887 1553619 Ppp3cc protein phosphatase 3, catalytic subunit, gamma isoform gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20231207 MGI 1553619 Ppp3cc protein phosphatase 3, catalytic subunit, gamma isoform gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20160818 MGI PMID:26429887 1553619 Ppp3cc protein phosphatase 3, catalytic subunit, gamma isoform gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20160818 MGI PMID:26429887 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20231207 MGI 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0001661 extended life span IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20231207 MGI 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20231207 MGI 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20231207 MGI 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20231207 MGI 1553620 Eprs1 glutamyl-prolyl-tRNA synthetase 1 gene MP:0014173 increased fatty acid beta-oxidation IAGP N RGD:5509061 20180531 MGI PMID:28178239 1553621 Timmdc1 translocase of inner mitochondrial membrane domain containing 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201022 MGI 1553621 Timmdc1 translocase of inner mitochondrial membrane domain containing 1 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1553621 Timmdc1 translocase of inner mitochondrial membrane domain containing 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1553621 Timmdc1 translocase of inner mitochondrial membrane domain containing 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1553621 Timmdc1 translocase of inner mitochondrial membrane domain containing 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20141003 MGI 1553621 Timmdc1 translocase of inner mitochondrial membrane domain containing 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1553621 Timmdc1 translocase of inner mitochondrial membrane domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 1553625 Mak16 MAK16 homolog gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1553625 Mak16 MAK16 homolog gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553625 Mak16 MAK16 homolog gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1553626 Als2cl ALS2 C-terminal like gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1553628 Klhl10 kelch-like 10 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1553628 Klhl10 kelch-like 10 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1553628 Klhl10 kelch-like 10 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15136734 1553628 Klhl10 kelch-like 10 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15136734 1553628 Klhl10 kelch-like 10 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15136734 1553628 Klhl10 kelch-like 10 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15136734 1553628 Klhl10 kelch-like 10 gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:15136734 1553628 Klhl10 kelch-like 10 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15136734 1553628 Klhl10 kelch-like 10 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15136734 1553630 Gpatch4 G patch domain containing 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1553630 Gpatch4 G patch domain containing 4 gene MP:0000692 small spleen IEA N RGD:5509061 20240523 MGI 1553630 Gpatch4 G patch domain containing 4 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20240523 MGI 1553630 Gpatch4 G patch domain containing 4 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20240523 MGI 1553630 Gpatch4 G patch domain containing 4 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1553630 Gpatch4 G patch domain containing 4 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 1553630 Gpatch4 G patch domain containing 4 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1553630 Gpatch4 G patch domain containing 4 gene MP:0005387 immune system phenotype IEA N RGD:5509061 20240523 MGI 1553630 Gpatch4 G patch domain containing 4 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 1553630 Gpatch4 G patch domain containing 4 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20240523 MGI 1553630 Gpatch4 G patch domain containing 4 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1553630 Gpatch4 G patch domain containing 4 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20240523 MGI 1553632 Klf6 Kruppel-like transcription factor 6 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:16234353 1553632 Klf6 Kruppel-like transcription factor 6 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20200310 MGI PMID:16234353 1553632 Klf6 Kruppel-like transcription factor 6 gene MP:0001163 abnormal prostate gland anterior lobe morphology IAGP N RGD:5509061 20200310 MGI PMID:19494112 1553632 Klf6 Kruppel-like transcription factor 6 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:17297474 1553632 Klf6 Kruppel-like transcription factor 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:16234353 1553632 Klf6 Kruppel-like transcription factor 6 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20200310 MGI PMID:16234353 1553632 Klf6 Kruppel-like transcription factor 6 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:17297474 1553632 Klf6 Kruppel-like transcription factor 6 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:16234353 1553632 Klf6 Kruppel-like transcription factor 6 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:16234353 1553632 Klf6 Kruppel-like transcription factor 6 gene MP:0003717 pallor IAGP N RGD:5509061 20200310 MGI PMID:16234353 1553632 Klf6 Kruppel-like transcription factor 6 gene MP:0009734 abnormal prostate gland duct morphology IAGP N RGD:5509061 20200310 MGI PMID:19494112 1553632 Klf6 Kruppel-like transcription factor 6 gene MP:0009736 abnormal prostate gland branching morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:19494112 1553632 Klf6 Kruppel-like transcription factor 6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16234353 1553636 Mrgprd MAS-related GPR, member D gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20190215 MGI PMID:30339496 1553636 Mrgprd MAS-related GPR, member D gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:19571152 1553636 Mrgprd MAS-related GPR, member D gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15629699 1553636 Mrgprd MAS-related GPR, member D gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19846708 1553636 Mrgprd MAS-related GPR, member D gene MP:0002626 increased heart rate IAGP N RGD:5509061 20190215 MGI PMID:30339496 1553636 Mrgprd MAS-related GPR, member D gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:19451647 1553636 Mrgprd MAS-related GPR, member D gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20190215 MGI PMID:30339496 1553636 Mrgprd MAS-related GPR, member D gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19451647 1553636 Mrgprd MAS-related GPR, member D gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20190215 MGI PMID:30339496 1553636 Mrgprd MAS-related GPR, member D gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:19571152 1553636 Mrgprd MAS-related GPR, member D gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20190215 MGI PMID:30339496 1553636 Mrgprd MAS-related GPR, member D gene MP:0004937 dilated heart IAGP N RGD:5509061 20190215 MGI PMID:30339496 1553636 Mrgprd MAS-related GPR, member D gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20190215 MGI PMID:30339496 1553636 Mrgprd MAS-related GPR, member D gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:19451647 1553636 Mrgprd MAS-related GPR, member D gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:19571152 1553636 Mrgprd MAS-related GPR, member D gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20190215 MGI PMID:30339496 1553636 Mrgprd MAS-related GPR, member D gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:17553423 1553636 Mrgprd MAS-related GPR, member D gene MP:0008726 increased heart left atrium size IAGP N RGD:5509061 20190215 MGI PMID:30339496 1553636 Mrgprd MAS-related GPR, member D gene MP:0010511 shortened PR interval IEA N RGD:5509061 20220519 MGI 1553636 Mrgprd MAS-related GPR, member D gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20231109 MGI PMID:30339496 1553636 Mrgprd MAS-related GPR, member D gene MP:0010613 abnormal mitral valve annulus morphology IAGP N RGD:5509061 20190215 MGI PMID:30339496 1553636 Mrgprd MAS-related GPR, member D gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20190215 MGI PMID:30339496 1553636 Mrgprd MAS-related GPR, member D gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20190215 MGI PMID:30339496 1553636 Mrgprd MAS-related GPR, member D gene MP:0020374 abnormal nocifensive behavior IAGP N RGD:5509061 20210204 MGI PMID:32084332 1553636 Mrgprd MAS-related GPR, member D gene MP:0020955 increased mechanical nociceptive threshold IAGP N RGD:5509061 20210204 MGI PMID:32084332 1553636 Mrgprd MAS-related GPR, member D gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:30339496 1553636 Mrgprd MAS-related GPR, member D gene MP:0031511 globular heart IAGP N RGD:5509061 20231109 MGI PMID:30339496 1553638 Pdxk pyridoxal (pyridoxine, vitamin B6) kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553639 Clec3b C-type lectin domain family 3, member b gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:11604516 1553639 Clec3b C-type lectin domain family 3, member b gene MP:0000160 kyphosis IAGP N RGD:5509061 20200310 MGI PMID:11604516 1553639 Clec3b C-type lectin domain family 3, member b gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20200310 MGI PMID:11604516 1553639 Clec3b C-type lectin domain family 3, member b gene MP:0005227 abnormal vertebral body development IAGP N RGD:5509061 20200310 MGI PMID:11604516 1553639 Clec3b C-type lectin domain family 3, member b gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20200310 MGI PMID:11604516 1553639 Clec3b C-type lectin domain family 3, member b gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20200310 MGI PMID:11604516 1553639 Clec3b C-type lectin domain family 3, member b gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1553639 Clec3b C-type lectin domain family 3, member b gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:11604516 1553642 Zfp697 zinc finger protein 697 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20240523 MGI 1553644 Vwf Von Willebrand factor gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9689113 1553644 Vwf Von Willebrand factor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18688020 1553644 Vwf Von Willebrand factor gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:10930441 1553644 Vwf Von Willebrand factor gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:9689113 1553644 Vwf Von Willebrand factor gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20201210 MGI PMID:30565388 1553644 Vwf Von Willebrand factor gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20181220 MGI PMID:27212476 1553644 Vwf Von Willebrand factor gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:19182208 1553644 Vwf Von Willebrand factor gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20181220 MGI PMID:27212476 1553644 Vwf Von Willebrand factor gene MP:0003292 melena IAGP N RGD:5509061 20141003 MGI PMID:9689113 1553644 Vwf Von Willebrand factor gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:18083848 1553644 Vwf Von Willebrand factor gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:18688020 1553644 Vwf Von Willebrand factor gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20181220 MGI PMID:27212476 1553644 Vwf Von Willebrand factor gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20181220 MGI PMID:27212476 1553644 Vwf Von Willebrand factor gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11520791 1553644 Vwf Von Willebrand factor gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:9689113 1553644 Vwf Von Willebrand factor gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20181220 MGI PMID:27212476 1553644 Vwf Von Willebrand factor gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20201210 MGI PMID:30565388 1553644 Vwf Von Willebrand factor gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20181220 MGI PMID:27212476 1553644 Vwf Von Willebrand factor gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:18084279 1553644 Vwf Von Willebrand factor gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:9689113 1553644 Vwf Von Willebrand factor gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20150611 MGI PMID:25293780 1553644 Vwf Von Willebrand factor gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20181220 MGI PMID:27212476 1553644 Vwf Von Willebrand factor gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20201210 MGI PMID:30565388 1553644 Vwf Von Willebrand factor gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:19182208 1553644 Vwf Von Willebrand factor gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:18084279 1553644 Vwf Von Willebrand factor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18083848 1553644 Vwf Von Willebrand factor gene MP:0009548 abnormal platelet aggregation IAGP N RGD:5509061 20181220 MGI PMID:27212476 1553644 Vwf Von Willebrand factor gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20181220 MGI PMID:27212476 1553644 Vwf Von Willebrand factor gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18083848 1553644 Vwf Von Willebrand factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10930441 1553644 Vwf Von Willebrand factor gene MP:0012359 increased partial thromboplastin time IAGP N RGD:5509061 20201001 MGI PMID:9689113 1553644 Vwf Von Willebrand factor gene MP:0020215 impaired blood coagulation IAGP N RGD:5509061 20150611 MGI PMID:25293780 1553644 Vwf Von Willebrand factor gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:11520791 1553644 Vwf Von Willebrand factor gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:27212476 1553644 Vwf Von Willebrand factor gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201001 MGI PMID:10930441 1553644 Vwf Von Willebrand factor gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201001 MGI PMID:18083848 1553644 Vwf Von Willebrand factor gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201210 MGI PMID:30565388 1553644 Vwf Von Willebrand factor gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:18688020 1553646 Ndufa11 NADH:ubiquinone oxidoreductase subunit A11 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20241010 MGI 1553646 Ndufa11 NADH:ubiquinone oxidoreductase subunit A11 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20241010 MGI 1553646 Ndufa11 NADH:ubiquinone oxidoreductase subunit A11 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20241010 MGI 1553646 Ndufa11 NADH:ubiquinone oxidoreductase subunit A11 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20241010 MGI 1553646 Ndufa11 NADH:ubiquinone oxidoreductase subunit A11 gene MP:0009331 absent primitive node IEA N RGD:5509061 20241010 MGI 1553646 Ndufa11 NADH:ubiquinone oxidoreductase subunit A11 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1553646 Ndufa11 NADH:ubiquinone oxidoreductase subunit A11 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1553646 Ndufa11 NADH:ubiquinone oxidoreductase subunit A11 gene MP:0012724 absent head fold IEA N RGD:5509061 20241010 MGI 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0000071 axial skeleton hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:18539921 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0000071 axial skeleton hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0000071 axial skeleton hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:23479625 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0000071 axial skeleton hypoplasia IAGP N RGD:5509061 20201029 MGI PMID:30865697 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20201029 MGI PMID:30865697 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20200310 MGI PMID:18539921 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20200310 MGI PMID:23479625 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0000435 shortened head IAGP N RGD:5509061 20200310 MGI PMID:18539921 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0000435 shortened head IAGP N RGD:5509061 20200310 MGI PMID:23479625 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0000445 short snout IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:18539921 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:23479625 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20201029 MGI PMID:30865697 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0001177 atelectasis IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0001260 increased body weight IEA N RGD:5509061 20200310 MGI 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20200310 MGI PMID:18539921 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:18539921 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20200310 MGI PMID:18539921 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20201029 MGI PMID:30865697 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0002765 short fibula IAGP N RGD:5509061 20201029 MGI PMID:30865697 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20200310 MGI PMID:18539921 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0003109 short femur IAGP N RGD:5509061 20201029 MGI PMID:30865697 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004321 short sternum IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004321 short sternum IAGP N RGD:5509061 20200310 MGI PMID:23479625 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004321 short sternum IAGP N RGD:5509061 20201029 MGI PMID:30865697 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004340 short scapula IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004340 short scapula IAGP N RGD:5509061 20200310 MGI PMID:23479625 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20200310 MGI PMID:23479625 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004355 short radius IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004355 short radius IAGP N RGD:5509061 20200310 MGI PMID:23479625 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20200310 MGI PMID:23479625 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20200310 MGI PMID:18539921 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20200310 MGI PMID:23479625 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20201029 MGI PMID:30865697 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004672 short ribs IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0004672 short ribs IAGP N RGD:5509061 20200310 MGI PMID:23479625 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20201029 MGI PMID:30865697 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20200310 MGI PMID:18539921 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20200310 MGI PMID:23479625 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20201029 MGI PMID:30865697 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20200310 MGI PMID:18539921 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18695242 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23479625 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20201029 MGI PMID:30865697 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0030245 round head IAGP N RGD:5509061 20200310 MGI PMID:18539921 1553656 Bpnt2 3'(2'), 5'-bisphosphate nucleotidase 2 gene MP:0030837 abnormal knee joint morphology IAGP N RGD:5509061 20200310 MGI PMID:18539921 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210128 MGI 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0000248 macrocytosis IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:19188446 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0001265 decreased body size IAGP N RGD:5509061 20180719 MGI PMID:8098731 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0001265 decreased body size IAGP N RGD:5509061 20180719 MGI PMID:9256469 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20180719 MGI PMID:11067886 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20180719 MGI PMID:8810244 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20180719 MGI PMID:11602620 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20180719 MGI PMID:11937578 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20180719 MGI PMID:7679955 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:9256469 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20180719 MGI PMID:10384121 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20180719 MGI PMID:11290790 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20180719 MGI PMID:9256469 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20180719 MGI PMID:10384121 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20180719 MGI PMID:19587020 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20210527 MGI PMID:24983315 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180719 MGI PMID:11602620 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180719 MGI PMID:11602620 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180719 MGI PMID:11937578 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20180719 MGI PMID:10843678 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20230601 MGI 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180719 MGI PMID:23267015 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20180719 MGI PMID:9551884 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005041 abnormal antigen presentation via MHC class II IAGP N RGD:5509061 20180719 MGI PMID:10384121 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005041 abnormal antigen presentation via MHC class II IAGP N RGD:5509061 20180719 MGI PMID:11290790 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005041 abnormal antigen presentation via MHC class II IAGP N RGD:5509061 20180719 MGI PMID:12646641 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005041 abnormal antigen presentation via MHC class II IAGP N RGD:5509061 20180719 MGI PMID:15034026 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005041 abnormal antigen presentation via MHC class II IAGP N RGD:5509061 20180719 MGI PMID:7553002 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005041 abnormal antigen presentation via MHC class II IAGP N RGD:5509061 20180719 MGI PMID:8098731 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005041 abnormal antigen presentation via MHC class II IAGP N RGD:5509061 20180719 MGI PMID:8977190 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20180719 MGI PMID:7553002 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20180719 MGI PMID:8098731 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20180719 MGI PMID:8294875 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20180719 MGI PMID:8977190 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20180719 MGI PMID:9551884 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005043 defective assembly of class II molecules IAGP N RGD:5509061 20180719 MGI PMID:7553002 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005043 defective assembly of class II molecules IAGP N RGD:5509061 20180719 MGI PMID:8098731 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005043 defective assembly of class II molecules IAGP N RGD:5509061 20180719 MGI PMID:8977190 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:16484589 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:8810244 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:10384121 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:11602620 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:7553002 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005150 cachexia IAGP N RGD:5509061 20180719 MGI PMID:8098731 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:7553002 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20180719 MGI PMID:11937578 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20180719 MGI PMID:11937578 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20180719 MGI PMID:12634786 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:10384121 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:11290790 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:15034026 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:7553002 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:7679955 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:8098731 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:8810244 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:9256469 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:9551884 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:7679955 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20180719 MGI PMID:9256469 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20180719 MGI PMID:23267015 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20180719 MGI PMID:23267013 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20180719 MGI PMID:10384121 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20180719 MGI PMID:11602620 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20180719 MGI PMID:11602620 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20180719 MGI PMID:11067886 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0013657 abnormal blood cell morphology IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0013705 decreased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20180719 MGI PMID:19966810 1553657 Cd74 CD74 antigen (invariant polypeptide of major histocompatibility complex, class II antigen-associated) gene MP:0031217 increased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20210527 MGI PMID:24983315 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20151126 MGI PMID:25965569 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:11239462 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11239462 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20151126 MGI PMID:25965569 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20151126 MGI PMID:25965569 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0001603 failure of myelopoiesis IAGP N RGD:5509061 20151126 MGI PMID:25965569 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20151126 MGI PMID:25965569 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11239462 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:11239462 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:14963485 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20151126 MGI PMID:25965569 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20151126 MGI PMID:25965569 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20151126 MGI PMID:25965569 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:11239462 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20151126 MGI PMID:25965569 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11239462 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20151126 MGI PMID:25965569 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:11239462 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11239462 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14963485 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:14963485 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20151126 MGI PMID:25965569 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:14963485 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20151126 MGI PMID:25965569 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20151126 MGI PMID:25965569 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14963485 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0013741 absent thymus corticomedullary boundary IAGP N RGD:5509061 20150430 MGI PMID:11239462 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0013776 bone marrow failure IAGP N RGD:5509061 20151126 MGI PMID:25965569 1553658 Srsf2 serine and arginine-rich splicing factor 2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:14963485 1553660 Zer1 zyg-11 related, cell cycle regulator gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1553660 Zer1 zyg-11 related, cell cycle regulator gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1553660 Zer1 zyg-11 related, cell cycle regulator gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 1553662 Pck2 phosphoenolpyruvate carboxykinase 2 (mitochondrial) gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20220519 MGI 1553662 Pck2 phosphoenolpyruvate carboxykinase 2 (mitochondrial) gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1553662 Pck2 phosphoenolpyruvate carboxykinase 2 (mitochondrial) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1553662 Pck2 phosphoenolpyruvate carboxykinase 2 (mitochondrial) gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20210826 MGI 1553662 Pck2 phosphoenolpyruvate carboxykinase 2 (mitochondrial) gene MP:0004930 small epididymis IEA N RGD:5509061 20220519 MGI 1553664 Ift140 intraflagellar transport 140 gene MP:0000075 absent neurocranium IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0000080 abnormal exoccipital bone morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0000111 cleft palate IEA N RGD:5509061 20200310 MGI 1553664 Ift140 intraflagellar transport 140 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20200310 MGI PMID:23469164 1553664 Ift140 intraflagellar transport 140 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200310 MGI PMID:23469164 1553664 Ift140 intraflagellar transport 140 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20200310 MGI PMID:22282595 1553664 Ift140 intraflagellar transport 140 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:23469164 1553664 Ift140 intraflagellar transport 140 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0000690 absent spleen IEA N RGD:5509061 20200310 MGI 1553664 Ift140 intraflagellar transport 140 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:23469164 1553664 Ift140 intraflagellar transport 140 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200310 MGI PMID:23469164 1553664 Ift140 intraflagellar transport 140 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0001925 male infertility IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:22282595 1553664 Ift140 intraflagellar transport 140 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20200310 MGI PMID:22282595 1553664 Ift140 intraflagellar transport 140 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20200310 MGI 1553664 Ift140 intraflagellar transport 140 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0003051 curly tail IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0003052 omphalocele IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0003054 spina bifida IAGP N RGD:5509061 20200310 MGI PMID:23469164 1553664 Ift140 intraflagellar transport 140 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0003178 left pulmonary isomerism IEA N RGD:5509061 20200310 MGI 1553664 Ift140 intraflagellar transport 140 gene MP:0003606 kidney failure IAGP N RGD:5509061 20200310 MGI PMID:22282595 1553664 Ift140 intraflagellar transport 140 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:22282595 1553664 Ift140 intraflagellar transport 140 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20200310 MGI PMID:22282595 1553664 Ift140 intraflagellar transport 140 gene MP:0004113 abnormal aortic arch morphology IEA N RGD:5509061 20200310 MGI 1553664 Ift140 intraflagellar transport 140 gene MP:0004158 right aortic arch IEA N RGD:5509061 20200310 MGI 1553664 Ift140 intraflagellar transport 140 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0004458 absent alisphenoid bone IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20200310 MGI PMID:22282595 1553664 Ift140 intraflagellar transport 140 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20200310 MGI PMID:22282595 1553664 Ift140 intraflagellar transport 140 gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0008149 abnormal costovertebral joint morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220317 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0009837 abnormal sperm end piece morphology IAGP N RGD:5509061 20220217 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0009877 exostosis IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20200310 MGI 1553664 Ift140 intraflagellar transport 140 gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22282595 1553664 Ift140 intraflagellar transport 140 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23469164 1553664 Ift140 intraflagellar transport 140 gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20200310 MGI PMID:22282595 1553664 Ift140 intraflagellar transport 140 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20200310 MGI PMID:22282595 1553664 Ift140 intraflagellar transport 140 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:22282595 1553664 Ift140 intraflagellar transport 140 gene MP:0013167 abnormal hindlimb bud morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:23469164 1553664 Ift140 intraflagellar transport 140 gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0020383 decreased kidney epithelial cell primary cilium length IAGP N RGD:5509061 20200310 MGI PMID:22282595 1553664 Ift140 intraflagellar transport 140 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220210 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0030385 absent facial bone IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0030386 facial bone hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:24009529 1553664 Ift140 intraflagellar transport 140 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20220317 MGI PMID:29236364 1553664 Ift140 intraflagellar transport 140 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220317 MGI PMID:29236364 1553666 Vps13a vacuolar protein sorting 13A gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20200310 MGI PMID:15686477 1553666 Vps13a vacuolar protein sorting 13A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:15686477 1553666 Vps13a vacuolar protein sorting 13A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:15686477 1553666 Vps13a vacuolar protein sorting 13A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:15686477 1553666 Vps13a vacuolar protein sorting 13A gene MP:0001407 short stride length IAGP N RGD:5509061 20200310 MGI PMID:15686477 1553666 Vps13a vacuolar protein sorting 13A gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:29928881 1553666 Vps13a vacuolar protein sorting 13A gene MP:0002183 gliosis IAGP N RGD:5509061 20200310 MGI PMID:15686477 1553666 Vps13a vacuolar protein sorting 13A gene MP:0002204 abnormal synaptic neurotransmitter level IAGP N RGD:5509061 20200310 MGI PMID:15686477 1553666 Vps13a vacuolar protein sorting 13A gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20200310 MGI PMID:15686477 1553666 Vps13a vacuolar protein sorting 13A gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:29928881 1553666 Vps13a vacuolar protein sorting 13A gene MP:0003242 loss of basal ganglia neurons IAGP N RGD:5509061 20200310 MGI PMID:15686477 1553666 Vps13a vacuolar protein sorting 13A gene MP:0008124 decreased plasmacytoid dendritic cell number IEA N RGD:5509061 20201231 MGI 1553666 Vps13a vacuolar protein sorting 13A gene MP:0010177 acanthocytosis IAGP N RGD:5509061 20200310 MGI PMID:15686477 1553666 Vps13a vacuolar protein sorting 13A gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20200310 MGI PMID:15686477 1553666 Vps13a vacuolar protein sorting 13A gene MP:0013764 decreased T-helper cell number IEA N RGD:5509061 20201231 MGI 1553666 Vps13a vacuolar protein sorting 13A gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:29928881 1553666 Vps13a vacuolar protein sorting 13A gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:15686477 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20201022 MGI 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0001406 abnormal gait IEA N RGD:5509061 20230601 MGI 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0005355 enlarged thyroid gland IEA N RGD:5509061 20201022 MGI 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0013519 decreased CD4-positive NK T cell number IEA N RGD:5509061 20210128 MGI 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0013696 increased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0013769 increased marginal zone precursor B cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553668 Pdia6 protein disulfide isomerase associated 6 gene MP:0013893 decreased common lymphocyte progenitor cell number IAGP N RGD:5509061 20201001 MGI PMID:31985756 1553672 Atp13a4 ATPase type 13A4 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1553672 Atp13a4 ATPase type 13A4 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20240523 MGI 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9918574 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20152175 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22952456 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:20152175 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:20703245 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:20703245 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20181227 MGI 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15458925 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:16260585 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:20703245 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12391252 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17623652 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18757438 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:17623652 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:20703245 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17992256 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:20703245 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22952456 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12391252 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20141003 MGI PMID:11433347 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:17640968 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:22952456 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:22952456 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:12511586 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20141003 MGI PMID:15458925 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0005085 abnormal gallbladder physiology IAGP N RGD:5509061 20141003 MGI PMID:17431214 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:17640968 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17992256 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:16691196 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:18156206 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11859856 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:15647743 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:12759239 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:16260585 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:14576054 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16434493 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:16434493 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:16434493 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12511586 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17304351 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12511586 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16434493 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:18757438 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18757438 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18757438 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9918574 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20703245 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9918574 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16434493 1553673 F2rl1 F2R like trypsin receptor 1 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:11086091 1553676 Tspan17 tetraspanin 17 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1553676 Tspan17 tetraspanin 17 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20211021 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0000111 cleft palate IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20210930 MGI PMID:31087039 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0000497 abnormal small intestine placement IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0001914 hemorrhage IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0001925 male infertility IAGP N RGD:5509061 20210930 MGI PMID:31087039 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20180201 MGI PMID:28931820 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20210930 MGI PMID:31087039 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210930 MGI PMID:31087039 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20180201 MGI PMID:28931820 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20210930 MGI PMID:31087039 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0002928 abnormal bile duct morphology IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0002989 small kidney IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:28931820 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20210930 MGI PMID:31087039 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20180201 MGI PMID:28931820 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20210930 MGI PMID:31087039 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20210930 MGI PMID:31087039 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20180201 MGI PMID:28931820 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20210930 MGI PMID:31087039 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20180201 MGI PMID:28931820 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20210930 MGI PMID:31087039 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0009234 absent sperm head IAGP N RGD:5509061 20210930 MGI PMID:31087039 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20210930 MGI PMID:31087039 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0010439 abnormal hepatic vein morphology IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0013970 absent connection between subcutaneous lymph vessels and lymph sac IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1553679 Tent5c terminal nucleotidyltransferase 5C gene MP:0014003 additional anastomosis between intracranial vertebral arteries IEA N RGD:5509061 20170504 MGI 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:31469588 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:31469588 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:31469588 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:31469588 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20200310 MGI PMID:31469588 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:31469588 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20200310 MGI PMID:31469588 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20200310 MGI PMID:31469588 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0005039 hypoxia IAGP N RGD:5509061 20180111 MGI PMID:28204537 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:31469588 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0005563 abnormal hemoglobin content IAGP N RGD:5509061 20180111 MGI PMID:28204537 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20200310 MGI PMID:31469588 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:31469588 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20200310 MGI PMID:31469588 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20160804 MGI 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160804 MGI 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20200310 MGI PMID:31469588 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0012552 lactic acidosis IAGP N RGD:5509061 20200310 MGI PMID:31469588 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1553681 Sdhc succinate dehydrogenase complex, subunit C, integral membrane protein gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20200310 MGI PMID:31469588 1553682 Paqr5 progestin and adipoQ receptor family member V gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1553682 Paqr5 progestin and adipoQ receptor family member V gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20240523 MGI 1553682 Paqr5 progestin and adipoQ receptor family member V gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20240523 MGI 1553682 Paqr5 progestin and adipoQ receptor family member V gene MP:0003068 enlarged kidney IEA N RGD:5509061 20240523 MGI 1553682 Paqr5 progestin and adipoQ receptor family member V gene MP:0003917 increased kidney weight IEA N RGD:5509061 20240523 MGI 1553683 Krt2 keratin 2 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 1553683 Krt2 keratin 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210805 MGI 1553683 Krt2 keratin 2 gene MP:0001147 small testis IEA N RGD:5509061 20210805 MGI 1553683 Krt2 keratin 2 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:12533510 1553683 Krt2 keratin 2 gene MP:0001192 scaly skin IAGP N RGD:5509061 20161027 MGI PMID:24751727 1553683 Krt2 keratin 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:12533510 1553683 Krt2 keratin 2 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20161027 MGI PMID:24751727 1553683 Krt2 keratin 2 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20161027 MGI PMID:24751727 1553683 Krt2 keratin 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20161027 MGI PMID:24751727 1553683 Krt2 keratin 2 gene MP:0001874 acanthosis IAGP N RGD:5509061 20161027 MGI PMID:24751727 1553683 Krt2 keratin 2 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 1553683 Krt2 keratin 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210805 MGI 1553683 Krt2 keratin 2 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20161027 MGI PMID:24751727 1553683 Krt2 keratin 2 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20161027 MGI PMID:24751727 1553683 Krt2 keratin 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210805 MGI 1553683 Krt2 keratin 2 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20161027 MGI PMID:24751727 1553683 Krt2 keratin 2 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210805 MGI 1553683 Krt2 keratin 2 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20161027 MGI PMID:24751727 1553683 Krt2 keratin 2 gene MP:0009599 thick epidermis stratum granulosum IAGP N RGD:5509061 20161027 MGI PMID:24751727 1553683 Krt2 keratin 2 gene MP:0009600 hypergranulosis IAGP N RGD:5509061 20161027 MGI PMID:24751727 1553683 Krt2 keratin 2 gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20161027 MGI PMID:24751727 1553683 Krt2 keratin 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 1553683 Krt2 keratin 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210805 MGI 1553683 Krt2 keratin 2 gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 1553683 Krt2 keratin 2 gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 1553683 Krt2 keratin 2 gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20161027 MGI PMID:24751727 1553683 Krt2 keratin 2 gene MP:0030605 abnormal corneocyte morphology IAGP N RGD:5509061 20180628 MGI PMID:24751727 1553684 Gpatch3 G patch domain containing 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1553684 Gpatch3 G patch domain containing 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1553684 Gpatch3 G patch domain containing 3 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1553684 Gpatch3 G patch domain containing 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1553684 Gpatch3 G patch domain containing 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1553684 Gpatch3 G patch domain containing 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1553684 Gpatch3 G patch domain containing 3 gene MP:0009084 blind uterus IEA N RGD:5509061 20201022 MGI 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16510570 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16510570 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12874803 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:12874803 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12874803 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16510570 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16510570 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12874803 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16510570 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:16510570 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12874803 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16510570 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15924147 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12874803 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15924147 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15924147 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12874803 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:12874803 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:12874803 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:15924147 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15924147 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16510570 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15924147 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:15924147 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19729480 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16510570 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1553686 Hmga1 high mobility group AT-hook 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12874803 1553690 Fibcd1 fibrinogen C domain containing 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20240808 MGI PMID:34937773 1553690 Fibcd1 fibrinogen C domain containing 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20240808 MGI PMID:34937773 1553690 Fibcd1 fibrinogen C domain containing 1 gene MP:0005398 decreased susceptibility to fungal infection IAGP N RGD:5509061 20240808 MGI PMID:34937773 1553690 Fibcd1 fibrinogen C domain containing 1 gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20240808 MGI PMID:34937773 1553690 Fibcd1 fibrinogen C domain containing 1 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20240808 MGI PMID:34937773 1553690 Fibcd1 fibrinogen C domain containing 1 gene MP:0009786 decreased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20240808 MGI PMID:34937773 1553690 Fibcd1 fibrinogen C domain containing 1 gene MP:0014433 increased cytokine level IAGP N RGD:5509061 20240808 MGI PMID:34937773 1553690 Fibcd1 fibrinogen C domain containing 1 gene MP:0014434 decreased cytokine level IAGP N RGD:5509061 20240808 MGI PMID:34937773 1553692 Snai1 snail family zinc finger 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:17376812 1553692 Snai1 snail family zinc finger 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17376812 1553692 Snai1 snail family zinc finger 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20150903 MGI PMID:24894949 1553692 Snai1 snail family zinc finger 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16801545 1553692 Snai1 snail family zinc finger 1 gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20150903 MGI PMID:24894949 1553692 Snai1 snail family zinc finger 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:17376812 1553692 Snai1 snail family zinc finger 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16801545 1553692 Snai1 snail family zinc finger 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:11689706 1553692 Snai1 snail family zinc finger 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:16397867 1553692 Snai1 snail family zinc finger 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:11689706 1553692 Snai1 snail family zinc finger 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11689706 1553692 Snai1 snail family zinc finger 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20150903 MGI PMID:24894949 1553692 Snai1 snail family zinc finger 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:16801545 1553692 Snai1 snail family zinc finger 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16397867 1553692 Snai1 snail family zinc finger 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17376812 1553692 Snai1 snail family zinc finger 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150903 MGI PMID:24894949 1553692 Snai1 snail family zinc finger 1 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:16801545 1553692 Snai1 snail family zinc finger 1 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:19188491 1553692 Snai1 snail family zinc finger 1 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20150903 MGI PMID:24894949 1553692 Snai1 snail family zinc finger 1 gene MP:0003891 increased allantois apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16801545 1553692 Snai1 snail family zinc finger 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11689706 1553692 Snai1 snail family zinc finger 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16801545 1553692 Snai1 snail family zinc finger 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20150903 MGI PMID:24894949 1553692 Snai1 snail family zinc finger 1 gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:16801545 1553692 Snai1 snail family zinc finger 1 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:16801545 1553692 Snai1 snail family zinc finger 1 gene MP:0004378 frontal bone foramen IAGP N RGD:5509061 20141003 MGI PMID:17376812 1553692 Snai1 snail family zinc finger 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20150903 MGI PMID:24894949 1553692 Snai1 snail family zinc finger 1 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:11689706 1553692 Snai1 snail family zinc finger 1 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17376812 1553692 Snai1 snail family zinc finger 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20150903 MGI PMID:24894949 1553692 Snai1 snail family zinc finger 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19188491 1553692 Snai1 snail family zinc finger 1 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16801545 1553692 Snai1 snail family zinc finger 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:16801545 1553692 Snai1 snail family zinc finger 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20150903 MGI PMID:24894949 1553692 Snai1 snail family zinc finger 1 gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20150903 MGI PMID:24894949 1553692 Snai1 snail family zinc finger 1 gene MP:0009593 absent chorion IAGP N RGD:5509061 20141003 MGI PMID:11689706 1553692 Snai1 snail family zinc finger 1 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:17376812 1553692 Snai1 snail family zinc finger 1 gene MP:0009889 persistence of medial edge epithelium during palatal shelf fusion IAGP N RGD:5509061 20141003 MGI PMID:17376812 1553692 Snai1 snail family zinc finger 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17376812 1553692 Snai1 snail family zinc finger 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16397867 1553692 Snai1 snail family zinc finger 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11689706 1553692 Snai1 snail family zinc finger 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16801545 1553692 Snai1 snail family zinc finger 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20150903 MGI PMID:24894949 1553692 Snai1 snail family zinc finger 1 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20150903 MGI PMID:24894949 1553692 Snai1 snail family zinc finger 1 gene MP:0030280 short parietal bone IAGP N RGD:5509061 20171207 MGI PMID:17376812 1553692 Snai1 snail family zinc finger 1 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:17376812 1553694 Cxxc5 CXXC finger 5 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20240314 MGI PMID:35390758 1553694 Cxxc5 CXXC finger 5 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0004348 long femur IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0008159 increased diameter of fibula IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0008162 increased diameter of tibia IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0008957 abnormal placenta junctional zone morphology IAGP N RGD:5509061 20240314 MGI PMID:35390758 1553694 Cxxc5 CXXC finger 5 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0011504 abnormal limb long bone morphology IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0011519 abnormal placenta labyrinth size IAGP N RGD:5509061 20240314 MGI PMID:35390758 1553694 Cxxc5 CXXC finger 5 gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0013149 macrodactyly IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20160225 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:25633194 1553694 Cxxc5 CXXC finger 5 gene MP:0030487 abnormal osteocyte dendritic process morphology IAGP N RGD:5509061 20171221 MGI PMID:25633194 1553696 Pan2 PAN2 poly(A) specific ribonuclease subunit gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1553696 Pan2 PAN2 poly(A) specific ribonuclease subunit gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1553696 Pan2 PAN2 poly(A) specific ribonuclease subunit gene MP:0008762 embryonic lethality IEA N RGD:5509061 20141003 MGI 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000746 weakness IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20200310 MGI PMID:20832057 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20200310 MGI PMID:14627648 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20200310 MGI PMID:20832057 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20200310 MGI PMID:14627648 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000884 delaminated Purkinje cell layer IAGP N RGD:5509061 20200310 MGI PMID:14627648 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:20832057 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:24802945 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20200310 MGI PMID:15992381 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20200310 MGI PMID:23064382 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20200310 MGI PMID:24802945 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20200310 MGI PMID:15992381 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20200310 MGI PMID:24725413 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20200310 MGI PMID:24802945 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20200310 MGI PMID:24802945 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:16407116 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0002064 seizures IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20200310 MGI PMID:20832057 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20200310 MGI PMID:14627648 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0002883 chromatolysis IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20200310 MGI PMID:24725413 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20200310 MGI PMID:24725413 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20200310 MGI PMID:23064382 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0003927 increased cellular glucose import IAGP N RGD:5509061 20200310 MGI PMID:20832057 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0008440 abnormal subplate morphology IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:20832057 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0009718 absent Purkinje cell layer IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:20832057 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15992381 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15992381 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20200310 MGI PMID:20832057 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11517264 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0011624 abnormal sensitization to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:20832057 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0012318 slow extinction of fear memory IAGP N RGD:5509061 20200310 MGI PMID:24725413 1553698 Cdk5r1 cyclin dependent kinase 5, regulatory subunit 1 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20200310 MGI PMID:9010203 1553700 Ctnna1 catenin alpha 1 gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:16543460 1553700 Ctnna1 catenin alpha 1 gene MP:0000448 pointed snout IAGP N RGD:5509061 20141003 MGI PMID:11239416 1553700 Ctnna1 catenin alpha 1 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16543460 1553700 Ctnna1 catenin alpha 1 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16543460 1553700 Ctnna1 catenin alpha 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:16543460 1553700 Ctnna1 catenin alpha 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11239416 1553700 Ctnna1 catenin alpha 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:11239416 1553700 Ctnna1 catenin alpha 1 gene MP:0001230 epidermal desquamation IAGP N RGD:5509061 20141003 MGI PMID:11239416 1553700 Ctnna1 catenin alpha 1 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:11239416 1553700 Ctnna1 catenin alpha 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11239416 1553700 Ctnna1 catenin alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14706703 1553700 Ctnna1 catenin alpha 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230511 MGI PMID:33497368 1553700 Ctnna1 catenin alpha 1 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:11239416 1553700 Ctnna1 catenin alpha 1 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20230511 MGI PMID:33497368 1553700 Ctnna1 catenin alpha 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20230511 MGI PMID:33497368 1553700 Ctnna1 catenin alpha 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14706703 1553700 Ctnna1 catenin alpha 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16543460 1553700 Ctnna1 catenin alpha 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20230511 MGI PMID:33497368 1553700 Ctnna1 catenin alpha 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9023354 1553700 Ctnna1 catenin alpha 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9023354 1553700 Ctnna1 catenin alpha 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:21924256 1553700 Ctnna1 catenin alpha 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:16543460 1553700 Ctnna1 catenin alpha 1 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:16543460 1553700 Ctnna1 catenin alpha 1 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11239416 1553700 Ctnna1 catenin alpha 1 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:9023354 1553700 Ctnna1 catenin alpha 1 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20151203 MGI PMID:26142281 1553700 Ctnna1 catenin alpha 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:22421363 1553700 Ctnna1 catenin alpha 1 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20161222 MGI PMID:26691986 1553700 Ctnna1 catenin alpha 1 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:21924256 1553700 Ctnna1 catenin alpha 1 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20160609 MGI PMID:21924256 1553700 Ctnna1 catenin alpha 1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:11239416 1553700 Ctnna1 catenin alpha 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:11239416 1553700 Ctnna1 catenin alpha 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:14706703 1553700 Ctnna1 catenin alpha 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:14706703 1553700 Ctnna1 catenin alpha 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20161222 MGI PMID:26691986 1553700 Ctnna1 catenin alpha 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:16543460 1553700 Ctnna1 catenin alpha 1 gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:14706703 1553700 Ctnna1 catenin alpha 1 gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:9023354 1553700 Ctnna1 catenin alpha 1 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20161222 MGI PMID:26691986 1553700 Ctnna1 catenin alpha 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20161222 MGI PMID:26691986 1553700 Ctnna1 catenin alpha 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:18809908 1553700 Ctnna1 catenin alpha 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20161222 MGI PMID:26691986 1553700 Ctnna1 catenin alpha 1 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20230511 MGI PMID:33497368 1553700 Ctnna1 catenin alpha 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20230511 MGI PMID:33497368 1553700 Ctnna1 catenin alpha 1 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:11239416 1553700 Ctnna1 catenin alpha 1 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20161222 MGI PMID:26691986 1553700 Ctnna1 catenin alpha 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20161222 MGI PMID:26691986 1553700 Ctnna1 catenin alpha 1 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20161222 MGI PMID:26691986 1553700 Ctnna1 catenin alpha 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20230511 MGI PMID:33497368 1553700 Ctnna1 catenin alpha 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20161222 MGI PMID:26691986 1553700 Ctnna1 catenin alpha 1 gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14706703 1553700 Ctnna1 catenin alpha 1 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11239416 1553700 Ctnna1 catenin alpha 1 gene MP:0009715 thick epidermis stratum basale IAGP N RGD:5509061 20141003 MGI PMID:11239416 1553700 Ctnna1 catenin alpha 1 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20230511 MGI PMID:33497368 1553700 Ctnna1 catenin alpha 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16543460 1553700 Ctnna1 catenin alpha 1 gene MP:0010172 abnormal mammary gland epithelium physiology IAGP N RGD:5509061 20141003 MGI PMID:14706703 1553700 Ctnna1 catenin alpha 1 gene MP:0010236 abnormal retina outer limiting membrane morphology IAGP N RGD:5509061 20161222 MGI PMID:26691986 1553700 Ctnna1 catenin alpha 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16543460 1553700 Ctnna1 catenin alpha 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20230511 MGI PMID:33497368 1553700 Ctnna1 catenin alpha 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230511 MGI PMID:33497368 1553700 Ctnna1 catenin alpha 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9023354 1553700 Ctnna1 catenin alpha 1 gene MP:0012040 abnormal c-wave shape IAGP N RGD:5509061 20161222 MGI PMID:26691986 1553700 Ctnna1 catenin alpha 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20161222 MGI PMID:26691986 1553700 Ctnna1 catenin alpha 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20161222 MGI PMID:26691986 1553700 Ctnna1 catenin alpha 1 gene MP:0012671 retina spots IAGP N RGD:5509061 20161222 MGI PMID:26691986 1553700 Ctnna1 catenin alpha 1 gene MP:0014126 increased mammary gland apoptosis IAGP N RGD:5509061 20160317 MGI PMID:14706703 1553700 Ctnna1 catenin alpha 1 gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20230511 MGI PMID:33497368 1553706 Gcnt3 glucosaminyl (N-acetyl) transferase 3, mucin type gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:19349303 1553706 Gcnt3 glucosaminyl (N-acetyl) transferase 3, mucin type gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:19349303 1553706 Gcnt3 glucosaminyl (N-acetyl) transferase 3, mucin type gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:19349303 1553706 Gcnt3 glucosaminyl (N-acetyl) transferase 3, mucin type gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19349303 1553706 Gcnt3 glucosaminyl (N-acetyl) transferase 3, mucin type gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1553706 Gcnt3 glucosaminyl (N-acetyl) transferase 3, mucin type gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19349303 1553706 Gcnt3 glucosaminyl (N-acetyl) transferase 3, mucin type gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:19349303 1553706 Gcnt3 glucosaminyl (N-acetyl) transferase 3, mucin type gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:19349303 1553706 Gcnt3 glucosaminyl (N-acetyl) transferase 3, mucin type gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:19349303 1553712 Mettl15 methyltransferase like 15 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20220922 MGI PMID:35682734 1553712 Mettl15 methyltransferase like 15 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20220922 MGI PMID:35682734 1553712 Mettl15 methyltransferase like 15 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20220922 MGI PMID:35682734 1553712 Mettl15 methyltransferase like 15 gene MP:0012315 impaired learning IAGP N RGD:5509061 20220922 MGI PMID:35682734 1553712 Mettl15 methyltransferase like 15 gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20220922 MGI PMID:35682734 1553716 Ankrd24 ankyrin repeat domain 24 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20240523 MGI 1553716 Ankrd24 ankyrin repeat domain 24 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1553718 Tox4 TOX high mobility group box family member 4 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1553718 Tox4 TOX high mobility group box family member 4 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1553718 Tox4 TOX high mobility group box family member 4 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1553718 Tox4 TOX high mobility group box family member 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553719 St6galnac3 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 gene MP:0001304 cataract IEA N RGD:5509061 20200310 MGI 1553719 St6galnac3 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 1553719 St6galnac3 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20240523 MGI 1553719 St6galnac3 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20231102 MGI PMID:37386100 1553719 St6galnac3 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1553719 St6galnac3 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 gene MP:0031051 lymph node hemorrhage IAGP N RGD:5509061 20231102 MGI PMID:37386100 1553720 Aimp1 aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1553720 Aimp1 aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1553720 Aimp1 aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15681823 1553720 Aimp1 aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1553720 Aimp1 aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:15681823 1553720 Aimp1 aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20220519 MGI 1553720 Aimp1 aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20220519 MGI 1553720 Aimp1 aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20190502 MGI 1553721 Serinc2 serine incorporator 2 gene MP:0001513 limb grasping IEA N RGD:5509061 20220811 MGI 1553721 Serinc2 serine incorporator 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20231207 MGI 1553723 Ralb v-ral simian leukemia viral oncogene B gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20150108 MGI 1553723 Ralb v-ral simian leukemia viral oncogene B gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553723 Ralb v-ral simian leukemia viral oncogene B gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553723 Ralb v-ral simian leukemia viral oncogene B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553723 Ralb v-ral simian leukemia viral oncogene B gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553723 Ralb v-ral simian leukemia viral oncogene B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553723 Ralb v-ral simian leukemia viral oncogene B gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20201231 MGI 1553723 Ralb v-ral simian leukemia viral oncogene B gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553723 Ralb v-ral simian leukemia viral oncogene B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553723 Ralb v-ral simian leukemia viral oncogene B gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:23063435 1553724 Ankrd16 ankyrin repeat domain 16 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:29769718 1553724 Ankrd16 ankyrin repeat domain 16 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20200310 MGI PMID:29769718 1553724 Ankrd16 ankyrin repeat domain 16 gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:29769718 1553724 Ankrd16 ankyrin repeat domain 16 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:29769718 1553724 Ankrd16 ankyrin repeat domain 16 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:29769718 1553724 Ankrd16 ankyrin repeat domain 16 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29769718 1553726 Tars2 threonyl-tRNA synthetase 2, mitochondrial (putative) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1553726 Tars2 threonyl-tRNA synthetase 2, mitochondrial (putative) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1553726 Tars2 threonyl-tRNA synthetase 2, mitochondrial (putative) gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1553733 Aldh18a1 aldehyde dehydrogenase 18 family, member A1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20200310 MGI PMID:25340873 1553733 Aldh18a1 aldehyde dehydrogenase 18 family, member A1 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20200310 MGI PMID:25340873 1553733 Aldh18a1 aldehyde dehydrogenase 18 family, member A1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25340873 1553733 Aldh18a1 aldehyde dehydrogenase 18 family, member A1 gene MP:0011156 abnormal hypodermis fat layer morphology IAGP N RGD:5509061 20200310 MGI PMID:25340873 1553734 Ctnnal1 catenin alpha like 1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20230216 MGI PMID:32258033 1553734 Ctnnal1 catenin alpha like 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20230216 MGI PMID:32258033 1553734 Ctnnal1 catenin alpha like 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20230216 MGI PMID:32258033 1553734 Ctnnal1 catenin alpha like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:26416744 1553734 Ctnnal1 catenin alpha like 1 gene MP:0003044 impaired basement membrane formation IAGP N RGD:5509061 20230216 MGI PMID:32258033 1553734 Ctnnal1 catenin alpha like 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20230216 MGI PMID:32258033 1553734 Ctnnal1 catenin alpha like 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20230216 MGI PMID:32258033 1553734 Ctnnal1 catenin alpha like 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20230216 MGI PMID:32258033 1553734 Ctnnal1 catenin alpha like 1 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20230216 MGI PMID:32258033 1553734 Ctnnal1 catenin alpha like 1 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20230216 MGI PMID:32258033 1553737 Cuta cutA divalent cation tolerance homolog gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 1553737 Cuta cutA divalent cation tolerance homolog gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1553737 Cuta cutA divalent cation tolerance homolog gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1553737 Cuta cutA divalent cation tolerance homolog gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1553737 Cuta cutA divalent cation tolerance homolog gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210826 MGI 1553737 Cuta cutA divalent cation tolerance homolog gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1553738 Kif13b kinesin family member 13B gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20150122 MGI PMID:24469637 1553738 Kif13b kinesin family member 13B gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20200130 MGI PMID:31487503 1553738 Kif13b kinesin family member 13B gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20200402 MGI 1553738 Kif13b kinesin family member 13B gene MP:0000445 short snout IAGP N RGD:5509061 20200130 MGI PMID:31487503 1553738 Kif13b kinesin family member 13B gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20150122 MGI PMID:24469637 1553738 Kif13b kinesin family member 13B gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20200130 MGI PMID:31487503 1553738 Kif13b kinesin family member 13B gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 1553738 Kif13b kinesin family member 13B gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20150122 MGI PMID:24469637 1553738 Kif13b kinesin family member 13B gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200130 MGI PMID:31487503 1553738 Kif13b kinesin family member 13B gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20200130 MGI PMID:31487503 1553738 Kif13b kinesin family member 13B gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200130 MGI PMID:31487503 1553738 Kif13b kinesin family member 13B gene MP:0012329 increased circulating factor VIII level IAGP N RGD:5509061 20150122 MGI PMID:24469637 1553738 Kif13b kinesin family member 13B gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20200130 MGI PMID:31487503 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0000495 abnormal colon morphology IEA N RGD:5509061 20210128 MGI 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210520 MGI 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0000948 nonconvulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:18215623 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:23325226 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:23325226 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0001304 cataract IEA N RGD:5509061 20210520 MGI 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20201022 MGI 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20200514 MGI 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:18215623 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:18674745 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18674745 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:18215623 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:23325226 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0003444 abnormal neurotransmitter uptake IAGP N RGD:5509061 20141003 MGI PMID:18278042 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:18674745 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0004416 absent cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:18674745 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18674745 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0004495 decreased synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:18215623 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0004562 abnormal inner hair cell synaptic ribbon morphology IAGP N RGD:5509061 20141003 MGI PMID:18215623 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0004562 abnormal inner hair cell synaptic ribbon morphology IAGP N RGD:5509061 20141003 MGI PMID:18674745 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0004633 abnormal cochlear IHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:18674745 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18674745 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:18215623 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0004836 abnormal synaptic acetylcholine release IAGP N RGD:5509061 20141003 MGI PMID:18278042 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210520 MGI 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:18215623 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18215623 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200514 MGI 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0009253 abnormal sympathetic neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:23325226 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18278042 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:18278042 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18215623 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18674745 1553740 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:18278042 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20201022 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0000111 cleft palate IEA N RGD:5509061 20230601 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20210128 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0000603 pale liver IEA N RGD:5509061 20230601 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20230601 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210128 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20220519 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0009084 blind uterus IEA N RGD:5509061 20210520 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0010146 umbilical hernia IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22206015 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553742 Col27a1 collagen, type XXVII, alpha 1 gene MP:0030273 mandibular retrognathia IAGP N RGD:5509061 20171026 MGI PMID:22206015 1553743 Zfp24 zinc finger protein 24 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20080941 1553743 Zfp24 zinc finger protein 24 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:20080941 1553743 Zfp24 zinc finger protein 24 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:20080941 1553743 Zfp24 zinc finger protein 24 gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:20080941 1553743 Zfp24 zinc finger protein 24 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20080941 1553743 Zfp24 zinc finger protein 24 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20080941 1553743 Zfp24 zinc finger protein 24 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:20080941 1553743 Zfp24 zinc finger protein 24 gene MP:0004264 abnormal extraembryonic tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:17064688 1553743 Zfp24 zinc finger protein 24 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:17064688 1553743 Zfp24 zinc finger protein 24 gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:20080941 1553743 Zfp24 zinc finger protein 24 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:20080941 1553743 Zfp24 zinc finger protein 24 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17064688 1553743 Zfp24 zinc finger protein 24 gene MP:0011731 decreased myelin sheath thickness IEA N RGD:5509061 20141003 MGI 1553743 Zfp24 zinc finger protein 24 gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20141003 MGI 1553743 Zfp24 zinc finger protein 24 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:17064688 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12372254 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:12372254 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:12372254 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:17468400 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12372253 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12372254 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:12372254 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:15389319 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20150618 MGI PMID:23288164 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:16242143 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:17468400 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16242143 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16242143 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12454287 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16242143 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:22408025 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0001725 abnormal umbilical cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12372253 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12454287 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002083 premature death IAGP N RGD:5509061 20150618 MGI PMID:23288164 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:15389319 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16242143 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12372253 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12372254 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16242143 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20150618 MGI PMID:23288164 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:16242143 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20150618 MGI PMID:23288164 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:17468400 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12372253 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12372253 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22408025 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20150618 MGI PMID:23288164 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0003410 abnormal artery development IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17468400 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20150618 MGI PMID:23288164 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:22408025 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0004225 patent cardiac foramen ovale IAGP N RGD:5509061 20141003 MGI PMID:15389319 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:22408025 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12454287 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17468400 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22408025 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16242143 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17468400 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20150618 MGI PMID:23288164 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:12454287 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12454287 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006044 tricuspid valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006045 mitral valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006046 atrioventricular valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20150618 MGI PMID:23288164 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16242143 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20150618 MGI PMID:23288164 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006123 tricuspid valve atresia IAGP N RGD:5509061 20141003 MGI PMID:12372254 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006123 tricuspid valve atresia IAGP N RGD:5509061 20141003 MGI PMID:15389319 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006123 tricuspid valve atresia IAGP N RGD:5509061 20141003 MGI PMID:16242143 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006124 tricuspid valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006124 tricuspid valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:15389319 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006124 tricuspid valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:16242143 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:12372254 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:22408025 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0008824 absent interventricular septum membranous part IAGP N RGD:5509061 20141003 MGI PMID:12454287 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:17303760 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010017 visceral vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:12454287 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:12454287 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:12454287 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12372253 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15389319 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16242143 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17468400 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:12372253 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:12372254 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010405 ostium secundum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12372254 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12454287 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15389319 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17303760 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12372254 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010432 common ventricle IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010457 pulmonary artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:12372254 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20150618 MGI PMID:23288164 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20150618 MGI PMID:23288164 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010595 abnormal aortic valve cusp morphology IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20150618 MGI PMID:23288164 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010602 abnormal pulmonary valve cusp morphology IAGP N RGD:5509061 20141003 MGI PMID:12372254 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010602 abnormal pulmonary valve cusp morphology IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010617 thick mitral valve cusps IAGP N RGD:5509061 20141003 MGI PMID:16242143 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0010997 decreased aorta wall thickness IAGP N RGD:5509061 20141003 MGI PMID:16242143 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16242143 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12454287 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12372253 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12372254 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12454287 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15389319 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17468400 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17468400 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15680351 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:12372253 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0031584 thick semilunar valve IAGP N RGD:5509061 20240125 MGI PMID:23288164 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15297376 1553745 Hey2 hairy/enhancer-of-split related with YRPW motif 2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:23288164 1553746 Tssk5 testis-specific serine kinase 5 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1553751 Itpkc inositol 1,4,5-trisphosphate 3-kinase C gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:14517551 1553751 Itpkc inositol 1,4,5-trisphosphate 3-kinase C gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14517551 1553751 Itpkc inositol 1,4,5-trisphosphate 3-kinase C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14517551 1553751 Itpkc inositol 1,4,5-trisphosphate 3-kinase C gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:14517551 1553751 Itpkc inositol 1,4,5-trisphosphate 3-kinase C gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:14517551 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16720880 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:14975726 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16720880 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16720880 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17507393 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:14975726 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:10601039 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23453598 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:10601039 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:10601039 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:23453598 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:16049111 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:23453598 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000551 absent forelimb IAGP N RGD:5509061 20141003 MGI PMID:23453598 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000553 absent radius IAGP N RGD:5509061 20141003 MGI PMID:11101846 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:23453598 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:16308330 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:21832120 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000678 abnormal parathyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20150305 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:14975726 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:14975726 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20230727 MGI PMID:24368733 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000836 abnormal substantia nigra morphology IAGP N RGD:5509061 20141003 MGI PMID:19968985 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:21832120 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19968985 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20230727 MGI PMID:24368733 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:10751172 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000865 absent cerebellum vermis IAGP N RGD:5509061 20230727 MGI PMID:24368733 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000867 abnormal cerebellum anterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:10751172 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000867 abnormal cerebellum anterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:19968985 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10751172 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:19968985 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:23453598 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17507393 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:19968985 1553752 Fgf8 fibroblast growth factor 8 gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10601039 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19968985 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:16308330 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10751172 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:10421635 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:10421635 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:17507393 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:17507393 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:17507393 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17507393 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:10421635 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16308330 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12223416 1553752 Fgf8 fibroblast growth factor 8 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11101845 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19968985 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:17507393 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:11101845 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:11101845 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11101845 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:14975726 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19968985 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:23453598 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:16308330 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11101845 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20843859 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:17507393 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:14975726 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:18832392 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:16720880 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:10421635 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16720880 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:17507393 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:16720880 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003152 abnormal pillar cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17557302 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12574514 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12574514 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12574514 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:17557302 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17557302 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003395 abnormal subclavian artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:23453598 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003494 parathyroid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:16049111 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003631 nervous system phenotype IAGP N RGD:5509061 20230727 MGI PMID:24368733 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17557302 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003854 abnormal forelimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:16308330 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:11101846 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:16308330 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003856 abnormal hindlimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:11101846 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003856 abnormal hindlimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:16308330 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:11101846 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:16308330 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003872 absent heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:16720880 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16720880 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003877 abnormal serotonergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19968985 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:10421635 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003931 absent molars IAGP N RGD:5509061 20141003 MGI PMID:10601039 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:10601039 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23453598 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004044 aortic dissection IAGP N RGD:5509061 20141003 MGI PMID:14975726 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20141003 MGI PMID:16308330 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:14975726 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:12223416 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16696966 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:21364285 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:12223416 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:15996652 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004161 cervical aortic arch IAGP N RGD:5509061 20141003 MGI PMID:12223416 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004161 cervical aortic arch IAGP N RGD:5509061 20141003 MGI PMID:21364285 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004312 absent pillar cells IAGP N RGD:5509061 20141003 MGI PMID:17557302 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004318 absent incus IAGP N RGD:5509061 20141003 MGI PMID:10601039 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20231130 MGI PMID:16308330 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20141003 MGI PMID:10601039 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004575 small limb buds IAGP N RGD:5509061 20141003 MGI PMID:11101846 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004592 small mandible IAGP N RGD:5509061 20170921 MGI PMID:15996652 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:16720880 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:17507393 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004861 abnormal Raphe nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19968985 1553752 Fgf8 fibroblast growth factor 8 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:16049111 1553752 Fgf8 fibroblast growth factor 8 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:10421635 1553752 Fgf8 fibroblast growth factor 8 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:17507393 1553752 Fgf8 fibroblast growth factor 8 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:14975726 1553752 Fgf8 fibroblast growth factor 8 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:16308330 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:16049111 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10601039 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:18832392 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:21364285 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:16308330 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:11101846 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:16308330 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006306 abnormal nasal pit morphology IAGP N RGD:5509061 20150827 MGI PMID:25381013 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:18818193 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006331 abnormal patterning of the organ of Corti IAGP N RGD:5509061 20141003 MGI PMID:17557302 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:10601039 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12223416 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:19855134 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:10421635 1553752 Fgf8 fibroblast growth factor 8 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:18832392 1553752 Fgf8 fibroblast growth factor 8 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0008919 fused tarsal bones IAGP N RGD:5509061 20141003 MGI PMID:16308330 1553752 Fgf8 fibroblast growth factor 8 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:10751172 1553752 Fgf8 fibroblast growth factor 8 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:19968985 1553752 Fgf8 fibroblast growth factor 8 gene MP:0009039 absent inferior colliculus IAGP N RGD:5509061 20141003 MGI PMID:18480159 1553752 Fgf8 fibroblast growth factor 8 gene MP:0009039 absent inferior colliculus IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0009048 enlarged tectum IAGP N RGD:5509061 20141003 MGI PMID:18480159 1553752 Fgf8 fibroblast growth factor 8 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:10421635 1553752 Fgf8 fibroblast growth factor 8 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:17507393 1553752 Fgf8 fibroblast growth factor 8 gene MP:0009844 abnormal neural crest cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0009845 abnormal neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16720880 1553752 Fgf8 fibroblast growth factor 8 gene MP:0009893 cleft primary palate IAGP N RGD:5509061 20150827 MGI PMID:25381013 1553752 Fgf8 fibroblast growth factor 8 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20141003 MGI PMID:10601039 1553752 Fgf8 fibroblast growth factor 8 gene MP:0010241 abnormal aortic arch development IAGP N RGD:5509061 20141003 MGI PMID:12223416 1553752 Fgf8 fibroblast growth factor 8 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:14975726 1553752 Fgf8 fibroblast growth factor 8 gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:14975726 1553752 Fgf8 fibroblast growth factor 8 gene MP:0010432 common ventricle IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0010527 bicuspid pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:18832392 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19968985 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10601039 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16049111 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17557302 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19968985 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14975726 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10421635 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16720880 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23453598 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16720879 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011262 abnormal pharyngeal arch mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:16720880 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011354 absent renal glomerulus IAGP N RGD:5509061 20141003 MGI PMID:16049111 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16049111 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:10421635 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:9462741 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:19968985 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:12223416 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:15996652 1553752 Fgf8 fibroblast growth factor 8 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18818193 1553752 Fgf8 fibroblast growth factor 8 gene MP:0012179 abnormal splanchnic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16720880 1553752 Fgf8 fibroblast growth factor 8 gene MP:0012278 abnormal cardiogenic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:17507393 1553752 Fgf8 fibroblast growth factor 8 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:10421635 1553752 Fgf8 fibroblast growth factor 8 gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0012730 abnormal internal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14975726 1553752 Fgf8 fibroblast growth factor 8 gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0013268 second pharyngeal arch hypoplasia IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0013269 third pharyngeal arch hypoplasia IAGP N RGD:5509061 20150924 MGI PMID:20035084 1553752 Fgf8 fibroblast growth factor 8 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1553752 Fgf8 fibroblast growth factor 8 gene MP:0013574 ectopic parathyroid gland IAGP N RGD:5509061 20150305 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0014044 absent cardiac outflow tract IAGP N RGD:5509061 20160304 MGI PMID:16720880 1553752 Fgf8 fibroblast growth factor 8 gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:16049111 1553752 Fgf8 fibroblast growth factor 8 gene MP:0021211 unilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:25381013 1553752 Fgf8 fibroblast growth factor 8 gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20170928 MGI PMID:25381013 1553752 Fgf8 fibroblast growth factor 8 gene MP:0030334 absent sixth pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0030336 third pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20171116 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0030337 enlarged third pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0030340 absent fourth pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:14623825 1553752 Fgf8 fibroblast growth factor 8 gene MP:0030341 fourth pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20171116 MGI PMID:14623825 1553755 Plcz1 phospholipase C, zeta 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20180125 MGI PMID:28694258 1553755 Plcz1 phospholipase C, zeta 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 1553755 Plcz1 phospholipase C, zeta 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20180125 MGI PMID:28694258 1553755 Plcz1 phospholipase C, zeta 1 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20210128 MGI 1553755 Plcz1 phospholipase C, zeta 1 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20181227 MGI 1553755 Plcz1 phospholipase C, zeta 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1553755 Plcz1 phospholipase C, zeta 1 gene MP:0031013 abnormal egg activation IAGP N RGD:5509061 20200130 MGI PMID:28694258 1553755 Plcz1 phospholipase C, zeta 1 gene MP:0031014 polyspermy IAGP N RGD:5509061 20200130 MGI PMID:28694258 1553757 Prkd2 protein kinase D2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:27670070 1553757 Prkd2 protein kinase D2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210826 MGI 1553757 Prkd2 protein kinase D2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20200310 MGI 1553757 Prkd2 protein kinase D2 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20200310 MGI PMID:20819079 1553757 Prkd2 protein kinase D2 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20200310 MGI 1553757 Prkd2 protein kinase D2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1553757 Prkd2 protein kinase D2 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:20819079 1553757 Prkd2 protein kinase D2 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:27670070 1553757 Prkd2 protein kinase D2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:20819079 1553757 Prkd2 protein kinase D2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:20819079 1553757 Prkd2 protein kinase D2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:20819079 1553757 Prkd2 protein kinase D2 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20200310 MGI PMID:20819079 1553757 Prkd2 protein kinase D2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200310 MGI 1553757 Prkd2 protein kinase D2 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20230601 MGI 1553757 Prkd2 protein kinase D2 gene MP:0011940 decreased food intake IEA N RGD:5509061 20200310 MGI 1553757 Prkd2 protein kinase D2 gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20200310 MGI PMID:27670070 1553758 Paqr9 progestin and adipoQ receptor family member IX gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20201015 MGI PMID:30061575 1553763 Rxfp3 relaxin family peptide receptor 3 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 1553763 Rxfp3 relaxin family peptide receptor 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1553763 Rxfp3 relaxin family peptide receptor 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20200310 MGI PMID:25257104 1553763 Rxfp3 relaxin family peptide receptor 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:25257104 1553763 Rxfp3 relaxin family peptide receptor 3 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20211021 MGI 1553763 Rxfp3 relaxin family peptide receptor 3 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20231207 MGI 1553763 Rxfp3 relaxin family peptide receptor 3 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20230601 MGI 1553769 Gda guanine deaminase gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20200402 MGI 1553769 Gda guanine deaminase gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20200402 MGI 1553769 Gda guanine deaminase gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1553769 Gda guanine deaminase gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200402 MGI 1553769 Gda guanine deaminase gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1553769 Gda guanine deaminase gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20200402 MGI 1553769 Gda guanine deaminase gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1553769 Gda guanine deaminase gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20200402 MGI 1553769 Gda guanine deaminase gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1553769 Gda guanine deaminase gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1553769 Gda guanine deaminase gene MP:0013764 decreased T-helper cell number IEA N RGD:5509061 20201231 MGI 1553769 Gda guanine deaminase gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20201231 MGI 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0001925 male infertility IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0014467 increased sperm mitochondrial size IAGP N RGD:5509061 20240613 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0030591 absent sperm fibrous sheath IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553771 Lrrc46 leucine rich repeat containing 46 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20221110 MGI PMID:35955660 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0001202 skin photosensitivity IAGP N RGD:5509061 20200310 MGI PMID:12509261 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0001203 increased sensitivity to skin irradiation IAGP N RGD:5509061 20200310 MGI PMID:12509261 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:12509261 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210520 MGI 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210826 MGI 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:12509261 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200310 MGI PMID:22174697 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:25762674 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:25762674 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20200310 MGI PMID:12509261 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210826 MGI 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20200310 MGI PMID:25762674 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20200310 MGI PMID:12509261 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20200310 MGI PMID:12509261 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200310 MGI PMID:12509261 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0008918 microgliosis IAGP N RGD:5509061 20200310 MGI PMID:22174697 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:25762674 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0013787 photophobia IAGP N RGD:5509061 20200310 MGI PMID:12509261 1553774 Ercc8 excision repaiross-complementing rodent repair deficiency, complementation group 8 gene MP:0014409 decreased distortion product otoacoustic emission amplitude IAGP N RGD:5509061 20240405 MGI PMID:25762674 1553776 Cd300lf CD300 molecule like family member F gene MP:0000921 demyelination IAGP N RGD:5509061 20200310 MGI PMID:20038601 1553776 Cd300lf CD300 molecule like family member F gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20200310 MGI PMID:23123064 1553776 Cd300lf CD300 molecule like family member F gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20200310 MGI PMID:23123064 1553776 Cd300lf CD300 molecule like family member F gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20200310 MGI PMID:20038601 1553776 Cd300lf CD300 molecule like family member F gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200310 MGI PMID:20038601 1553776 Cd300lf CD300 molecule like family member F gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20200310 MGI PMID:23123064 1553776 Cd300lf CD300 molecule like family member F gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20200310 MGI PMID:23123064 1553776 Cd300lf CD300 molecule like family member F gene MP:0008654 increased interleukin-1 alpha secretion IAGP N RGD:5509061 20200310 MGI PMID:20038601 1553776 Cd300lf CD300 molecule like family member F gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:20038601 1553776 Cd300lf CD300 molecule like family member F gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20200310 MGI PMID:20038601 1553776 Cd300lf CD300 molecule like family member F gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20200310 MGI PMID:23123064 1553776 Cd300lf CD300 molecule like family member F gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20200310 MGI PMID:23123064 1553776 Cd300lf CD300 molecule like family member F gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20200310 MGI PMID:23123064 1553777 Id3 inhibitor of DNA binding 3 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20211021 MGI PMID:34434211 1553777 Id3 inhibitor of DNA binding 3 gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20200310 MGI PMID:16502419 1553777 Id3 inhibitor of DNA binding 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20200310 MGI PMID:15485632 1553777 Id3 inhibitor of DNA binding 3 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20200310 MGI PMID:20932862 1553777 Id3 inhibitor of DNA binding 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:21857655 1553777 Id3 inhibitor of DNA binding 3 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:10537105 1553777 Id3 inhibitor of DNA binding 3 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20200310 MGI PMID:22522171 1553777 Id3 inhibitor of DNA binding 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210520 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0001147 small testis IEA N RGD:5509061 20210520 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:10537105 1553777 Id3 inhibitor of DNA binding 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:21145943 1553777 Id3 inhibitor of DNA binding 3 gene MP:0001306 small lens IAGP N RGD:5509061 20200310 MGI PMID:21145943 1553777 Id3 inhibitor of DNA binding 3 gene MP:0001314 cornea opacity IEA N RGD:5509061 20231207 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0001346 abnormal lacrimal gland morphology IAGP N RGD:5509061 20200310 MGI PMID:15485632 1553777 Id3 inhibitor of DNA binding 3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210826 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20211021 MGI PMID:34434211 1553777 Id3 inhibitor of DNA binding 3 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20200310 MGI PMID:15485632 1553777 Id3 inhibitor of DNA binding 3 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:10537105 1553777 Id3 inhibitor of DNA binding 3 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200310 MGI PMID:15485632 1553777 Id3 inhibitor of DNA binding 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:10661402 1553777 Id3 inhibitor of DNA binding 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:17622570 1553777 Id3 inhibitor of DNA binding 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:20932862 1553777 Id3 inhibitor of DNA binding 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:22522171 1553777 Id3 inhibitor of DNA binding 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:10661402 1553777 Id3 inhibitor of DNA binding 3 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:10454544 1553777 Id3 inhibitor of DNA binding 3 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:10454544 1553777 Id3 inhibitor of DNA binding 3 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20231207 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:21145943 1553777 Id3 inhibitor of DNA binding 3 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:22522171 1553777 Id3 inhibitor of DNA binding 3 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20200310 MGI PMID:10537105 1553777 Id3 inhibitor of DNA binding 3 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20200310 MGI PMID:22522171 1553777 Id3 inhibitor of DNA binding 3 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:10537105 1553777 Id3 inhibitor of DNA binding 3 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20200310 MGI PMID:15485632 1553777 Id3 inhibitor of DNA binding 3 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20200310 MGI PMID:10537105 1553777 Id3 inhibitor of DNA binding 3 gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20211021 MGI PMID:34434211 1553777 Id3 inhibitor of DNA binding 3 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200310 MGI PMID:10537105 1553777 Id3 inhibitor of DNA binding 3 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200310 MGI PMID:21145943 1553777 Id3 inhibitor of DNA binding 3 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200310 MGI PMID:22522171 1553777 Id3 inhibitor of DNA binding 3 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:10537105 1553777 Id3 inhibitor of DNA binding 3 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200310 MGI PMID:21857655 1553777 Id3 inhibitor of DNA binding 3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:20932862 1553777 Id3 inhibitor of DNA binding 3 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:10454544 1553777 Id3 inhibitor of DNA binding 3 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20200310 MGI PMID:10537105 1553777 Id3 inhibitor of DNA binding 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:20932862 1553777 Id3 inhibitor of DNA binding 3 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:20932862 1553777 Id3 inhibitor of DNA binding 3 gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20200310 MGI PMID:20932862 1553777 Id3 inhibitor of DNA binding 3 gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20200310 MGI PMID:21857655 1553777 Id3 inhibitor of DNA binding 3 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20200310 MGI PMID:22522171 1553777 Id3 inhibitor of DNA binding 3 gene MP:0008879 submandibular gland inflammation IAGP N RGD:5509061 20200310 MGI PMID:20932862 1553777 Id3 inhibitor of DNA binding 3 gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20200310 MGI PMID:15485632 1553777 Id3 inhibitor of DNA binding 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210826 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20200310 MGI PMID:10537105 1553777 Id3 inhibitor of DNA binding 3 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20200310 MGI PMID:21145943 1553777 Id3 inhibitor of DNA binding 3 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20200310 MGI PMID:22522171 1553777 Id3 inhibitor of DNA binding 3 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20200310 MGI PMID:10537105 1553777 Id3 inhibitor of DNA binding 3 gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20200310 MGI PMID:21857655 1553777 Id3 inhibitor of DNA binding 3 gene MP:0010537 tumor regression IAGP N RGD:5509061 20200310 MGI PMID:10537105 1553777 Id3 inhibitor of DNA binding 3 gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20200310 MGI PMID:20932862 1553777 Id3 inhibitor of DNA binding 3 gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20200310 MGI PMID:20932862 1553777 Id3 inhibitor of DNA binding 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22522171 1553777 Id3 inhibitor of DNA binding 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10537105 1553777 Id3 inhibitor of DNA binding 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21145943 1553777 Id3 inhibitor of DNA binding 3 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9372963 1553777 Id3 inhibitor of DNA binding 3 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20200310 MGI PMID:22522171 1553777 Id3 inhibitor of DNA binding 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20211021 MGI PMID:34434211 1553777 Id3 inhibitor of DNA binding 3 gene MP:0013367 parotid gland inflammation IAGP N RGD:5509061 20200310 MGI PMID:20932862 1553777 Id3 inhibitor of DNA binding 3 gene MP:0014409 decreased distortion product otoacoustic emission amplitude IAGP N RGD:5509061 20240405 MGI PMID:34434211 1553777 Id3 inhibitor of DNA binding 3 gene MP:0020220 decreased tear production IAGP N RGD:5509061 20200310 MGI PMID:15485632 1553777 Id3 inhibitor of DNA binding 3 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1553777 Id3 inhibitor of DNA binding 3 gene MP:0030410 middle ear effusion IAGP N RGD:5509061 20211021 MGI PMID:34434211 1553781 Paf1 Paf1, RNA polymerase II complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553781 Paf1 Paf1, RNA polymerase II complex component gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1553782 Ndufa10 NADH:ubiquinone oxidoreductase subunit A10 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200514 MGI 1553782 Ndufa10 NADH:ubiquinone oxidoreductase subunit A10 gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 1553782 Ndufa10 NADH:ubiquinone oxidoreductase subunit A10 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20200514 MGI 1553782 Ndufa10 NADH:ubiquinone oxidoreductase subunit A10 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1553782 Ndufa10 NADH:ubiquinone oxidoreductase subunit A10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553784 Adpgk ADP-dependent glucokinase gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20200402 MGI 1553784 Adpgk ADP-dependent glucokinase gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200310 MGI 1553784 Adpgk ADP-dependent glucokinase gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200310 MGI 1553784 Adpgk ADP-dependent glucokinase gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1553784 Adpgk ADP-dependent glucokinase gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 1553787 Gnptg N-acetylglucosamine-1-phosphotransferase, gamma subunit gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 1553787 Gnptg N-acetylglucosamine-1-phosphotransferase, gamma subunit gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1553787 Gnptg N-acetylglucosamine-1-phosphotransferase, gamma subunit gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1553787 Gnptg N-acetylglucosamine-1-phosphotransferase, gamma subunit gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210520 MGI 1553787 Gnptg N-acetylglucosamine-1-phosphotransferase, gamma subunit gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 1553787 Gnptg N-acetylglucosamine-1-phosphotransferase, gamma subunit gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1553787 Gnptg N-acetylglucosamine-1-phosphotransferase, gamma subunit gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1553787 Gnptg N-acetylglucosamine-1-phosphotransferase, gamma subunit gene MP:0005238 increased brain size IEA N RGD:5509061 20210520 MGI 1553787 Gnptg N-acetylglucosamine-1-phosphotransferase, gamma subunit gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1553787 Gnptg N-acetylglucosamine-1-phosphotransferase, gamma subunit gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17652091 1553787 Gnptg N-acetylglucosamine-1-phosphotransferase, gamma subunit gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1553787 Gnptg N-acetylglucosamine-1-phosphotransferase, gamma subunit gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180830 MGI PMID:29208648 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20221103 MGI 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210520 MGI 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20180830 MGI PMID:29208648 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:16467571 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:16467571 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16467571 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221103 MGI 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15377789 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16467571 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20180830 MGI PMID:29208648 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16467571 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0003044 impaired basement membrane formation IAGP N RGD:5509061 20141003 MGI PMID:16467571 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0003954 abnormal Reichert's membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16467571 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15377789 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16467571 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20180830 MGI PMID:29208648 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:16467571 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16467571 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:16467571 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:15377789 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16467571 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180830 MGI PMID:29208648 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15377789 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16467571 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20180830 MGI PMID:29208648 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16467571 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 1553789 Plod3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene MP:0014239 abnormal intracellular organelle morphology IAGP N RGD:5509061 20230615 MGI PMID:15377789 1553792 Pxylp1 2-phosphoxylose phosphatase 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 1553792 Pxylp1 2-phosphoxylose phosphatase 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20160804 MGI 1553792 Pxylp1 2-phosphoxylose phosphatase 1 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1553792 Pxylp1 2-phosphoxylose phosphatase 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1553792 Pxylp1 2-phosphoxylose phosphatase 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 1553792 Pxylp1 2-phosphoxylose phosphatase 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1553792 Pxylp1 2-phosphoxylose phosphatase 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160804 MGI 1553793 Dhx40 DEAH-box helicase 40 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 1553793 Dhx40 DEAH-box helicase 40 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1553793 Dhx40 DEAH-box helicase 40 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20220811 MGI 1553793 Dhx40 DEAH-box helicase 40 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20161201 MGI 1553793 Dhx40 DEAH-box helicase 40 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1553793 Dhx40 DEAH-box helicase 40 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1553793 Dhx40 DEAH-box helicase 40 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1553793 Dhx40 DEAH-box helicase 40 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160804 MGI 1553793 Dhx40 DEAH-box helicase 40 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200402 MGI 1553793 Dhx40 DEAH-box helicase 40 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1553793 Dhx40 DEAH-box helicase 40 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 1553793 Dhx40 DEAH-box helicase 40 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1553793 Dhx40 DEAH-box helicase 40 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1553793 Dhx40 DEAH-box helicase 40 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220519 MGI 1553793 Dhx40 DEAH-box helicase 40 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1553794 Tnfsf12 tumor necrosis factor (ligand) superfamily, member 12 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16325585 1553794 Tnfsf12 tumor necrosis factor (ligand) superfamily, member 12 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16325585 1553794 Tnfsf12 tumor necrosis factor (ligand) superfamily, member 12 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16325585 1553794 Tnfsf12 tumor necrosis factor (ligand) superfamily, member 12 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:16325585 1553794 Tnfsf12 tumor necrosis factor (ligand) superfamily, member 12 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16325585 1553794 Tnfsf12 tumor necrosis factor (ligand) superfamily, member 12 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16325585 1553794 Tnfsf12 tumor necrosis factor (ligand) superfamily, member 12 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:16325585 1553794 Tnfsf12 tumor necrosis factor (ligand) superfamily, member 12 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16325585 1553794 Tnfsf12 tumor necrosis factor (ligand) superfamily, member 12 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:16325585 1553794 Tnfsf12 tumor necrosis factor (ligand) superfamily, member 12 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16325585 1553794 Tnfsf12 tumor necrosis factor (ligand) superfamily, member 12 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16325585 1553794 Tnfsf12 tumor necrosis factor (ligand) superfamily, member 12 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:16325585 1553794 Tnfsf12 tumor necrosis factor (ligand) superfamily, member 12 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:16325585 1553797 Kif11 kinesin family member 11 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18474226 1553797 Kif11 kinesin family member 11 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:18474226 1553797 Kif11 kinesin family member 11 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17449012 1553797 Kif11 kinesin family member 11 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:18474226 1553797 Kif11 kinesin family member 11 gene MP:0006204 embryonic lethality before implantation IAGP N RGD:5509061 20141003 MGI PMID:18474226 1553797 Kif11 kinesin family member 11 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:17449012 1553797 Kif11 kinesin family member 11 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17449012 1553797 Kif11 kinesin family member 11 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17449012 1553797 Kif11 kinesin family member 11 gene MP:0012111 failure of morula compaction IAGP N RGD:5509061 20141003 MGI PMID:17449012 1553804 Pfn2 profilin 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19497369 1553804 Pfn2 profilin 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19497369 1553804 Pfn2 profilin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19497369 1553804 Pfn2 profilin 2 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17541406 1553804 Pfn2 profilin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19497369 1553804 Pfn2 profilin 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17541406 1553804 Pfn2 profilin 2 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:17541406 1553804 Pfn2 profilin 2 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:17541406 1553804 Pfn2 profilin 2 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:17541406 1553804 Pfn2 profilin 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17541406 1553804 Pfn2 profilin 2 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:17541406 1553804 Pfn2 profilin 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17541406 1553807 1700088E04Rik RIKEN cDNA 1700088E04 gene gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20210128 MGI 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:16024815 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:16024815 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:16024815 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0001377 abnormal mating frequency IAGP N RGD:5509061 20200310 MGI PMID:16024815 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20210128 MGI 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:16024815 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20200310 MGI PMID:16024815 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20200310 MGI PMID:16024815 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20220811 MGI 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210128 MGI 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:16024815 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0004909 increased seminal vesicle weight IAGP N RGD:5509061 20200310 MGI PMID:16024815 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0004930 small epididymis IAGP N RGD:5509061 20200310 MGI PMID:16024815 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:16024815 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16024815 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16024815 1553808 Aff4 AF4/FMR2 family, member 4 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1553809 Plpp5 phospholipid phosphatase 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:30042348 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000128 growth retardation of molars IAGP N RGD:5509061 20180215 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:10631182 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9664686 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000155 asymmetric rib joints IAGP N RGD:5509061 20141003 MGI PMID:9664686 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9664686 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20150716 MGI PMID:25889639 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20160804 MGI 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:7590254 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:15342483 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:16154126 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:7590254 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:15342483 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:16154126 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:7590254 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:7590254 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9664686 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:7590254 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11784057 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:7590254 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:16154126 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:7590254 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:8792608 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11784057 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0001957 apnea IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002083 premature death IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:8792608 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9664686 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:7590254 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16154126 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17194222 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002244 abnormal turbinate morphology IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:11784057 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:10631182 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:11784057 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20160804 MGI 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20150716 MGI PMID:25889639 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20150716 MGI PMID:25889639 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:15342483 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003154 abnormal soft palate morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003445 sirenomelia IAGP N RGD:5509061 20150716 MGI PMID:23028455 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20150716 MGI PMID:25889639 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003670 dilated renal glomerular capsule IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:15342483 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:16154126 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003756 abnormal hard palate morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20141003 MGI PMID:11470817 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:10631182 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:10631182 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:10631182 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004456 small pterygoid bone IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004458 absent alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004459 small alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004468 small zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004539 absent maxilla IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004574 broad limb buds IAGP N RGD:5509061 20141003 MGI PMID:8792608 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004595 abnormal mandibular condyloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004612 fusion of vertebral bodies IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:9664686 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:10631182 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:9664686 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004679 xiphoid process foramen IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004757 abnormal distal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004790 absent upper incisors IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11784057 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004899 absent temporal bone squamous part IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004911 absent mandibular condyloid process IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004913 absent mandibular angle IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004934 epididymis epithelium degeneration IAGP N RGD:5509061 20141003 MGI PMID:11784057 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0004935 epididymis degeneration IAGP N RGD:5509061 20141003 MGI PMID:11784057 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:10631182 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:15342483 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11784057 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0006400 decreased molar number IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:7590254 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0009003 abnormal vibrissa number IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0009052 anal stenosis IAGP N RGD:5509061 20150716 MGI PMID:23028455 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0009252 absent urinary bladder IAGP N RGD:5509061 20150716 MGI PMID:23028455 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0009782 abnormal basicranium angle IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0010688 hair follicle outer root sheath hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0010985 abnormal kidney mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15342483 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7590254 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15342483 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17260385 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:9013703 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0011387 absent metanephric mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:7590255 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0011846 decreased kidney collecting duct number IAGP N RGD:5509061 20141003 MGI PMID:15342483 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:19247966 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0014291 decreased autopod size IAGP N RGD:5509061 20230824 MGI PMID:10631182 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0030026 small Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20171005 MGI PMID:22219353 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0030199 deviated nasal septum IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0030200 abnormal nasal septum cartilage morphology IAGP N RGD:5509061 20171012 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0030262 frontal bossing IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0030319 abnormal temporal bone petrous part morphology IAGP N RGD:5509061 20171109 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0030420 short basicranium IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0030681 increased circulating hydroxyproline level IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0030868 absent thyroid cartilage IAGP N RGD:5509061 20181101 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0030873 absent cricoid cartilage IAGP N RGD:5509061 20181101 MGI PMID:19127565 1553810 Bmp7 bone morphogenetic protein 7 gene MP:0031101 nasal obstruction IAGP N RGD:5509061 20210325 MGI PMID:33431521 1553811 Ibtk inhibitor of Bruton agammaglobulinemia tyrosine kinase gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20221215 MGI 1553811 Ibtk inhibitor of Bruton agammaglobulinemia tyrosine kinase gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:21482705 1553812 Derl1 Der1-like domain family, member 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:22479592 1553812 Derl1 Der1-like domain family, member 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22479592 1553817 Igsf5 immunoglobulin superfamily, member 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16982697 1553818 Gemin2 gem nuclear organelle associated protein 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:12091709 1553818 Gemin2 gem nuclear organelle associated protein 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12091709 1553819 Parp6 poly (ADP-ribose) polymerase family, member 6 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20220224 MGI PMID:34067418 1553819 Parp6 poly (ADP-ribose) polymerase family, member 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220224 MGI PMID:34067418 1553819 Parp6 poly (ADP-ribose) polymerase family, member 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220224 MGI PMID:34067418 1553819 Parp6 poly (ADP-ribose) polymerase family, member 6 gene MP:0001401 jumpy IAGP N RGD:5509061 20220224 MGI PMID:34067418 1553819 Parp6 poly (ADP-ribose) polymerase family, member 6 gene MP:0001575 cyanosis IAGP N RGD:5509061 20220224 MGI PMID:34067418 1553819 Parp6 poly (ADP-ribose) polymerase family, member 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20220224 MGI PMID:34067418 1553819 Parp6 poly (ADP-ribose) polymerase family, member 6 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20220224 MGI PMID:34067418 1553822 Slc22a18 solute carrier family 22 (organic cation transporter), member 18 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20240627 MGI PMID:38626531 1553822 Slc22a18 solute carrier family 22 (organic cation transporter), member 18 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20240627 MGI PMID:38626531 1553822 Slc22a18 solute carrier family 22 (organic cation transporter), member 18 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20240627 MGI PMID:38626531 1553824 Taar6 trace amine-associated receptor 6 gene MP:0005573 increased pulmonary respiratory rate IEA N RGD:5509061 20201022 MGI 1553824 Taar6 trace amine-associated receptor 6 gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 1553824 Taar6 trace amine-associated receptor 6 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1553824 Taar6 trace amine-associated receptor 6 gene MP:0012125 decreased bronchoconstrictive response IEA N RGD:5509061 20201022 MGI 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0000601 small liver IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0001263 weight loss IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0001505 hunched posture IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191205 MGI 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191205 MGI 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0002083 premature death IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0002083 premature death IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191205 MGI 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0008993 abnormal portal triad morphology IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0009331 absent primitive node IEA N RGD:5509061 20191205 MGI 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0012724 absent head fold IEA N RGD:5509061 20191205 MGI 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20181227 MGI 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220519 MGI 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20190509 MGI PMID:21274865 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0020836 increased circulating citrulline level IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0030650 increased circulating ornithine level IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0030662 decreased circulating arginine level IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0030970 ketosis IAGP N RGD:5509061 20200213 MGI PMID:28424480 1553825 Bcs1l BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21274865 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200310 MGI PMID:20538684 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:23593136 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20200310 MGI PMID:20538684 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20200310 MGI PMID:23593136 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20200310 MGI PMID:20538684 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:20538684 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20200310 MGI PMID:20538684 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:20538684 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20200310 MGI PMID:23593136 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20200310 MGI PMID:20538684 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20200310 MGI PMID:20538684 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:23593136 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20200310 MGI PMID:23593136 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20200310 MGI PMID:20538684 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0010695 abnormal blood pressure regulation IAGP N RGD:5509061 20200310 MGI PMID:20538684 1553828 Pdlim5 PDZ and LIM domain 5 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:20538684 1553829 Itga2 integrin alpha 2 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:12107118 1553829 Itga2 integrin alpha 2 gene MP:0000745 tremors IEA N RGD:5509061 20160421 MGI 1553829 Itga2 integrin alpha 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11788609 1553829 Itga2 integrin alpha 2 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:12107118 1553829 Itga2 integrin alpha 2 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:16636073 1553829 Itga2 integrin alpha 2 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:11788609 1553829 Itga2 integrin alpha 2 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:16618804 1553829 Itga2 integrin alpha 2 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:23359821 1553829 Itga2 integrin alpha 2 gene MP:0008935 decreased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:23359821 1553829 Itga2 integrin alpha 2 gene MP:0009548 abnormal platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:11788609 1553829 Itga2 integrin alpha 2 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:11788609 1553829 Itga2 integrin alpha 2 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:23359821 1553831 Usp6nl USP6 N-terminal like gene MP:0011709 increased fibroblast cell migration IAGP N RGD:5509061 20200310 MGI PMID:24239119 1553831 Usp6nl USP6 N-terminal like gene MP:0020417 increased fibroblast chemotaxis IAGP N RGD:5509061 20200310 MGI PMID:24239119 1553838 Mterf3 mitochondrial transcription termination factor 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:17662942 1553838 Mterf3 mitochondrial transcription termination factor 3 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17662942 1553838 Mterf3 mitochondrial transcription termination factor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17662942 1553838 Mterf3 mitochondrial transcription termination factor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17662942 1553838 Mterf3 mitochondrial transcription termination factor 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17662942 1553838 Mterf3 mitochondrial transcription termination factor 3 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:17662942 1553838 Mterf3 mitochondrial transcription termination factor 3 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:17662942 1553838 Mterf3 mitochondrial transcription termination factor 3 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:17662942 1553838 Mterf3 mitochondrial transcription termination factor 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17662942 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0000706 small thymus IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0008070 absent T cells IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0010134 decreased DN3 thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0012765 decreased alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:25201955 1553840 Noc2l NOC2 like nucleolar associated transcriptional repressor gene MP:0014257 embryonic lethality prior to tooth bud stage, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:25201955 1553847 Letm1 leucine zipper-EF-hand containing transmembrane protein 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20160714 MGI PMID:23716663 1553847 Letm1 leucine zipper-EF-hand containing transmembrane protein 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20160714 MGI PMID:23716663 1553847 Letm1 leucine zipper-EF-hand containing transmembrane protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160714 MGI PMID:23716663 1553847 Letm1 leucine zipper-EF-hand containing transmembrane protein 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20160714 MGI PMID:23716663 1553847 Letm1 leucine zipper-EF-hand containing transmembrane protein 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20160714 MGI PMID:23716663 1553847 Letm1 leucine zipper-EF-hand containing transmembrane protein 1 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20160714 MGI PMID:23716663 1553847 Letm1 leucine zipper-EF-hand containing transmembrane protein 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20160714 MGI PMID:23716663 1553847 Letm1 leucine zipper-EF-hand containing transmembrane protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160714 MGI PMID:23716663 1553847 Letm1 leucine zipper-EF-hand containing transmembrane protein 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20160714 MGI PMID:23716663 1553847 Letm1 leucine zipper-EF-hand containing transmembrane protein 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20160714 MGI PMID:23716663 1553847 Letm1 leucine zipper-EF-hand containing transmembrane protein 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20160714 MGI PMID:23716663 1553847 Letm1 leucine zipper-EF-hand containing transmembrane protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160714 MGI PMID:23716663 1553847 Letm1 leucine zipper-EF-hand containing transmembrane protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20160714 MGI PMID:23716663 1553847 Letm1 leucine zipper-EF-hand containing transmembrane protein 1 gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20160714 MGI PMID:23716663 1553848 Ush1c USH1 protein network component harmonin gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:19447093 1553848 Ush1c USH1 protein network component harmonin gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20160324 MGI PMID:24725409 1553848 Ush1c USH1 protein network component harmonin gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20160324 MGI PMID:24725409 1553848 Ush1c USH1 protein network component harmonin gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20160324 MGI PMID:24725409 1553848 Ush1c USH1 protein network component harmonin gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20160324 MGI PMID:24725409 1553848 Ush1c USH1 protein network component harmonin gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:14519688 1553848 Ush1c USH1 protein network component harmonin gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:14519688 1553848 Ush1c USH1 protein network component harmonin gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:17174357 1553848 Ush1c USH1 protein network component harmonin gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:19447093 1553848 Ush1c USH1 protein network component harmonin gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:20211154 1553848 Ush1c USH1 protein network component harmonin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17174357 1553848 Ush1c USH1 protein network component harmonin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20211154 1553848 Ush1c USH1 protein network component harmonin gene MP:0001408 stereotypic behavior IEA N RGD:5509061 20170105 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0001410 head bobbing IEA N RGD:5509061 20111116 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0001512 trunk curl IEA N RGD:5509061 20170105 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0001513 limb grasping IEA N RGD:5509061 20170105 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:20211154 1553848 Ush1c USH1 protein network component harmonin gene MP:0001523 impaired righting response IEA N RGD:5509061 20170105 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:14519688 1553848 Ush1c USH1 protein network component harmonin gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:14519688 1553848 Ush1c USH1 protein network component harmonin gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:19447093 1553848 Ush1c USH1 protein network component harmonin gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:20211154 1553848 Ush1c USH1 protein network component harmonin gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20211154 1553848 Ush1c USH1 protein network component harmonin gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:19447093 1553848 Ush1c USH1 protein network component harmonin gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20141003 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150108 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:14519688 1553848 Ush1c USH1 protein network component harmonin gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:14519688 1553848 Ush1c USH1 protein network component harmonin gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20211154 1553848 Ush1c USH1 protein network component harmonin gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20332152 1553848 Ush1c USH1 protein network component harmonin gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:14519688 1553848 Ush1c USH1 protein network component harmonin gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20141003 MGI PMID:19447093 1553848 Ush1c USH1 protein network component harmonin gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:20211154 1553848 Ush1c USH1 protein network component harmonin gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:20211154 1553848 Ush1c USH1 protein network component harmonin gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:19447093 1553848 Ush1c USH1 protein network component harmonin gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:18339676 1553848 Ush1c USH1 protein network component harmonin gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:14519688 1553848 Ush1c USH1 protein network component harmonin gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 1553848 Ush1c USH1 protein network component harmonin gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:18849963 1553848 Ush1c USH1 protein network component harmonin gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:20211154 1553848 Ush1c USH1 protein network component harmonin gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:20332152 1553848 Ush1c USH1 protein network component harmonin gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:14519688 1553848 Ush1c USH1 protein network component harmonin gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 1553848 Ush1c USH1 protein network component harmonin gene MP:0004577 abnormal cochlear hair cell inter-stereocilial links morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 1553848 Ush1c USH1 protein network component harmonin gene MP:0004578 abnormal cochlear hair bundle tip links morphology IAGP N RGD:5509061 20141003 MGI PMID:19447093 1553848 Ush1c USH1 protein network component harmonin gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:14519688 1553848 Ush1c USH1 protein network component harmonin gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:17174357 1553848 Ush1c USH1 protein network component harmonin gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:19447093 1553848 Ush1c USH1 protein network component harmonin gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:20211154 1553848 Ush1c USH1 protein network component harmonin gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20150108 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:17174357 1553848 Ush1c USH1 protein network component harmonin gene MP:0008141 decreased small intestinal microvillus size IAGP N RGD:5509061 20160324 MGI PMID:24725409 1553848 Ush1c USH1 protein network component harmonin gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20141003 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20141003 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0010053 decreased grip strength IEA N RGD:5509061 20141003 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20150108 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0011939 increased food intake IEA N RGD:5509061 20211021 MGI 1553848 Ush1c USH1 protein network component harmonin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:14519688 1553848 Ush1c USH1 protein network component harmonin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:19447093 1553848 Ush1c USH1 protein network component harmonin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20211154 1553848 Ush1c USH1 protein network component harmonin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:22381527 1553848 Ush1c USH1 protein network component harmonin gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20141003 MGI PMID:20211154 1553849 Ube2d3 ubiquitin-conjugating enzyme E2D 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20201022 MGI 1553849 Ube2d3 ubiquitin-conjugating enzyme E2D 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1553849 Ube2d3 ubiquitin-conjugating enzyme E2D 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20160421 MGI 1553849 Ube2d3 ubiquitin-conjugating enzyme E2D 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1553849 Ube2d3 ubiquitin-conjugating enzyme E2D 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1553854 Prickle3 prickle planar cell polarity protein 3 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20210415 MGI PMID:32516135 1553854 Prickle3 prickle planar cell polarity protein 3 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20210415 MGI PMID:32516135 1553854 Prickle3 prickle planar cell polarity protein 3 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20210415 MGI PMID:32516135 1553854 Prickle3 prickle planar cell polarity protein 3 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20210415 MGI PMID:32516135 1553854 Prickle3 prickle planar cell polarity protein 3 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20210415 MGI PMID:32516135 1553854 Prickle3 prickle planar cell polarity protein 3 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20210415 MGI PMID:32516135 1553854 Prickle3 prickle planar cell polarity protein 3 gene MP:0020339 abnormal retina ganglion cell dendrite morphology IAGP N RGD:5509061 20210415 MGI PMID:32516135 1553854 Prickle3 prickle planar cell polarity protein 3 gene MP:0031141 increased retina vascular tortuosity IAGP N RGD:5509061 20210415 MGI PMID:32516135 1553856 Klhl22 kelch-like 22 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20210826 MGI 1553856 Klhl22 kelch-like 22 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20211104 MGI PMID:33109719 1553856 Klhl22 kelch-like 22 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1553856 Klhl22 kelch-like 22 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20211104 MGI PMID:33109719 1553856 Klhl22 kelch-like 22 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20211104 MGI PMID:33109719 1553856 Klhl22 kelch-like 22 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20211104 MGI PMID:33109719 1553856 Klhl22 kelch-like 22 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20211104 MGI PMID:33109719 1553857 Nipsnap3b nipsnap homolog 3B gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20240523 MGI 1553857 Nipsnap3b nipsnap homolog 3B gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20240523 MGI 1553857 Nipsnap3b nipsnap homolog 3B gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20240523 MGI 1553862 Paqr6 progestin and adipoQ receptor family member VI gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 1553862 Paqr6 progestin and adipoQ receptor family member VI gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1553869 Tspan14 tetraspanin 14 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1553869 Tspan14 tetraspanin 14 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1553872 Chrdl1 chordin-like 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 1553872 Chrdl1 chordin-like 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20190718 MGI PMID:30344043 1553872 Chrdl1 chordin-like 1 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20190718 MGI PMID:30344043 1553872 Chrdl1 chordin-like 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20190718 MGI PMID:30344043 1553872 Chrdl1 chordin-like 1 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20211021 MGI 1553872 Chrdl1 chordin-like 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1553873 Lyzl4 lysozyme-like 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:27357688 1553878 Marchf2 membrane associated ring-CH-type finger 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20240523 MGI 1553878 Marchf2 membrane associated ring-CH-type finger 2 gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20210121 MGI PMID:32935379 1553878 Marchf2 membrane associated ring-CH-type finger 2 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20210121 MGI PMID:32935379 1553878 Marchf2 membrane associated ring-CH-type finger 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20240523 MGI 1553878 Marchf2 membrane associated ring-CH-type finger 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 1553878 Marchf2 membrane associated ring-CH-type finger 2 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20240523 MGI 1553878 Marchf2 membrane associated ring-CH-type finger 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20210121 MGI PMID:32935379 1553878 Marchf2 membrane associated ring-CH-type finger 2 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20210121 MGI PMID:32935379 1553878 Marchf2 membrane associated ring-CH-type finger 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20210121 MGI PMID:32935379 1553878 Marchf2 membrane associated ring-CH-type finger 2 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20210121 MGI PMID:32935379 1553878 Marchf2 membrane associated ring-CH-type finger 2 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20210121 MGI PMID:32935379 1553878 Marchf2 membrane associated ring-CH-type finger 2 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20210121 MGI PMID:32935379 1553878 Marchf2 membrane associated ring-CH-type finger 2 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20210121 MGI PMID:32935379 1553878 Marchf2 membrane associated ring-CH-type finger 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20210121 MGI PMID:32935379 1553879 Orc4 origin recognition complex, subunit 4 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20220721 MGI PMID:34977916 1553879 Orc4 origin recognition complex, subunit 4 gene MP:0001926 female infertility IAGP N RGD:5509061 20220721 MGI PMID:34977916 1553879 Orc4 origin recognition complex, subunit 4 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20220721 MGI PMID:34977916 1553879 Orc4 origin recognition complex, subunit 4 gene MP:0012736 abnormal polar body morphology IAGP N RGD:5509061 20220721 MGI PMID:34977916 1553882 Oas1h 2'-5' oligoadenylate synthetase 1H gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38786026 1553883 Bmf BCL2 modifying factor gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:19841067 1553883 Bmf BCL2 modifying factor gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:18299399 1553883 Bmf BCL2 modifying factor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18299399 1553883 Bmf BCL2 modifying factor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19841067 1553883 Bmf BCL2 modifying factor gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18299399 1553883 Bmf BCL2 modifying factor gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19841067 1553883 Bmf BCL2 modifying factor gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18299399 1553883 Bmf BCL2 modifying factor gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:19841067 1553883 Bmf BCL2 modifying factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19841067 1553883 Bmf BCL2 modifying factor gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18299399 1553883 Bmf BCL2 modifying factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19841067 1553883 Bmf BCL2 modifying factor gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:18299399 1553883 Bmf BCL2 modifying factor gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18299399 1553883 Bmf BCL2 modifying factor gene MP:0003537 hydrometrocolpos IAGP N RGD:5509061 20141003 MGI PMID:19841067 1553883 Bmf BCL2 modifying factor gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18299399 1553883 Bmf BCL2 modifying factor gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19841067 1553883 Bmf BCL2 modifying factor gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20161013 MGI PMID:27044867 1553883 Bmf BCL2 modifying factor gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18299399 1553883 Bmf BCL2 modifying factor gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19841067 1553883 Bmf BCL2 modifying factor gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19841067 1553883 Bmf BCL2 modifying factor gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19841067 1553883 Bmf BCL2 modifying factor gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19841067 1553883 Bmf BCL2 modifying factor gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18299399 1553883 Bmf BCL2 modifying factor gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18299399 1553883 Bmf BCL2 modifying factor gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18299399 1553883 Bmf BCL2 modifying factor gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18299399 1553883 Bmf BCL2 modifying factor gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18299399 1553883 Bmf BCL2 modifying factor gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:19841067 1553883 Bmf BCL2 modifying factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19841067 1553884 Neil2 nei like 2 (E. coli) gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1553884 Neil2 nei like 2 (E. coli) gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:26245904 1553884 Neil2 nei like 2 (E. coli) gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1553884 Neil2 nei like 2 (E. coli) gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:26245904 1553884 Neil2 nei like 2 (E. coli) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:26245904 1553884 Neil2 nei like 2 (E. coli) gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1553884 Neil2 nei like 2 (E. coli) gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:26245904 1553884 Neil2 nei like 2 (E. coli) gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20200310 MGI PMID:26245904 1553884 Neil2 nei like 2 (E. coli) gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1553884 Neil2 nei like 2 (E. coli) gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20220811 MGI 1553884 Neil2 nei like 2 (E. coli) gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1553884 Neil2 nei like 2 (E. coli) gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1553884 Neil2 nei like 2 (E. coli) gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20200310 MGI PMID:26245904 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20150226 MGI PMID:23118208 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23709686 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23709686 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0005014 increased B cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20150226 MGI PMID:23118208 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20150226 MGI PMID:23118208 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0008559 abnormal interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23709686 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23709686 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0008615 decreased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:23709686 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0008680 abnormal interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:23709686 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:23709686 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23602766 1553885 Clec4d C-type lectin domain family 4, member d gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23709686 1553887 Serpina12 serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22837305 1553887 Serpina12 serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22837305 1553887 Serpina12 serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22837305 1553887 Serpina12 serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22837305 1553887 Serpina12 serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22837305 1553887 Serpina12 serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22837305 1553887 Serpina12 serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22837305 1553887 Serpina12 serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22837305 1553887 Serpina12 serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22837305 1553887 Serpina12 serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22837305 1553888 Ryk receptor-like tyrosine kinase gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0000111 cleft palate IEA N RGD:5509061 20230601 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20230119 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20231207 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20230601 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230119 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0001785 edema IEA N RGD:5509061 20230601 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230119 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20230119 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20230119 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0009906 increased tongue size IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1553888 Ryk receptor-like tyrosine kinase gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20171026 MGI PMID:10932185 1553888 Ryk receptor-like tyrosine kinase gene MP:0030315 small neurocranium IAGP N RGD:5509061 20171109 MGI PMID:10932185 1553892 Reg4 regenerating islet-derived family, member 4 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20230601 MGI 1553892 Reg4 regenerating islet-derived family, member 4 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 1553892 Reg4 regenerating islet-derived family, member 4 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230601 MGI 15554233 Gm26330 predicted gene, 26330 gene MP:0001261 obese IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0001762 polyuria IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0011939 increased food intake IAGP N RGD:5509061 20231109 MGI PMID:37329887 15554233 Gm26330 predicted gene, 26330 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20231109 MGI PMID:37329887 15557747 Snord50b small nucleolar RNA, C/D box 50B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20201029 MGI PMID:23991050 15557747 Snord50b small nucleolar RNA, C/D box 50B gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20201029 MGI PMID:23991050 15557747 Snord50b small nucleolar RNA, C/D box 50B gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20201029 MGI PMID:23991050 15557747 Snord50b small nucleolar RNA, C/D box 50B gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20201029 MGI PMID:23991050 15557747 Snord50b small nucleolar RNA, C/D box 50B gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20201029 MGI PMID:23991050 15557747 Snord50b small nucleolar RNA, C/D box 50B gene MP:0005630 increased lung weight IAGP N RGD:5509061 20201029 MGI PMID:23991050 15557755 Snord50a small nucleolar RNA, C/D box 50A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20201029 MGI PMID:23991050 15557755 Snord50a small nucleolar RNA, C/D box 50A gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20201029 MGI PMID:23991050 15557755 Snord50a small nucleolar RNA, C/D box 50A gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20201029 MGI PMID:23991050 15557755 Snord50a small nucleolar RNA, C/D box 50A gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20201029 MGI PMID:23991050 15557755 Snord50a small nucleolar RNA, C/D box 50A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20201029 MGI PMID:23991050 15557755 Snord50a small nucleolar RNA, C/D box 50A gene MP:0005630 increased lung weight IAGP N RGD:5509061 20201029 MGI PMID:23991050 1556860 Itm2a integral membrane protein 2A gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23650549 1556860 Itm2a integral membrane protein 2A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23650549 1556861 Glb1l3 galactosidase, beta 1 like 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20221215 MGI 1556861 Glb1l3 galactosidase, beta 1 like 3 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 1556862 Tsnaxip1 translin-associated factor X (Tsnax) interacting protein 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20231012 MGI PMID:36598146 1556862 Tsnaxip1 translin-associated factor X (Tsnax) interacting protein 1 gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20231012 MGI PMID:36598146 1556862 Tsnaxip1 translin-associated factor X (Tsnax) interacting protein 1 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20231012 MGI PMID:36598146 1556865 Il22 interleukin 22 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23064362 1556865 Il22 interleukin 22 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:18264109 1556865 Il22 interleukin 22 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:24211183 1556865 Il22 interleukin 22 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:17187052 1556865 Il22 interleukin 22 gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:17187052 1556865 Il22 interleukin 22 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18264109 1556865 Il22 interleukin 22 gene MP:0001655 multifocal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:18264109 1556865 Il22 interleukin 22 gene MP:0001849 ear inflammation IAGP N RGD:5509061 20141003 MGI PMID:17187052 1556865 Il22 interleukin 22 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:17919941 1556865 Il22 interleukin 22 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:22038916 1556865 Il22 interleukin 22 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:17187052 1556865 Il22 interleukin 22 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:23223145 1556865 Il22 interleukin 22 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20150514 MGI PMID:25261485 1556865 Il22 interleukin 22 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:18264109 1556865 Il22 interleukin 22 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:23223145 1556865 Il22 interleukin 22 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17919941 1556865 Il22 interleukin 22 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17187052 1556865 Il22 interleukin 22 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1556865 Il22 interleukin 22 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1556865 Il22 interleukin 22 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23075849 1556865 Il22 interleukin 22 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18264109 1556865 Il22 interleukin 22 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:24211183 1556865 Il22 interleukin 22 gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:23223145 1556865 Il22 interleukin 22 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17919941 1556865 Il22 interleukin 22 gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:22038916 1556865 Il22 interleukin 22 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:23075849 1556865 Il22 interleukin 22 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22038916 1556865 Il22 interleukin 22 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:22038916 1556865 Il22 interleukin 22 gene MP:0008618 decreased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:22038916 1556865 Il22 interleukin 22 gene MP:0008639 decreased circulating interleukin-1 alpha level IAGP N RGD:5509061 20141003 MGI PMID:22038916 1556865 Il22 interleukin 22 gene MP:0008648 decreased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:22038916 1556865 Il22 interleukin 22 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:23064362 1556865 Il22 interleukin 22 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17919941 1556865 Il22 interleukin 22 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17919941 1556865 Il22 interleukin 22 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23064362 1556865 Il22 interleukin 22 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20210617 MGI PMID:33753942 1556865 Il22 interleukin 22 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18264109 1556865 Il22 interleukin 22 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20150514 MGI PMID:25261485 1556865 Il22 interleukin 22 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:22038916 1556865 Il22 interleukin 22 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24211183 1556865 Il22 interleukin 22 gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23075849 1556865 Il22 interleukin 22 gene MP:0020186 abnormal susceptibility to bacterial infection IAGP N RGD:5509061 20150514 MGI PMID:25261485 1556866 Phlpp2 PH domain and leucine rich repeat protein phosphatase 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1556866 Phlpp2 PH domain and leucine rich repeat protein phosphatase 2 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20160929 MGI PMID:26187040 1556866 Phlpp2 PH domain and leucine rich repeat protein phosphatase 2 gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20160929 MGI PMID:26187040 1556867 Anks1b ankyrin repeat and sterile alpha motif domain containing 1B gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20170817 MGI PMID:28115237 1556867 Anks1b ankyrin repeat and sterile alpha motif domain containing 1B gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20160707 MGI PMID:26085624 1556867 Anks1b ankyrin repeat and sterile alpha motif domain containing 1B gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20160707 MGI PMID:26085624 1556867 Anks1b ankyrin repeat and sterile alpha motif domain containing 1B gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20170817 MGI PMID:28115237 1556867 Anks1b ankyrin repeat and sterile alpha motif domain containing 1B gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20170817 MGI PMID:28115237 1556867 Anks1b ankyrin repeat and sterile alpha motif domain containing 1B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170817 MGI PMID:28115237 1556867 Anks1b ankyrin repeat and sterile alpha motif domain containing 1B gene MP:0011274 short excitatory postsynaptic current decay time IAGP N RGD:5509061 20160707 MGI PMID:26085624 1556867 Anks1b ankyrin repeat and sterile alpha motif domain containing 1B gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:28115237 1556868 Or55b4 olfactory receptor family 55 subfamily B member 4 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20240314 MGI PMID:28990936 1556870 Cep72 centrosomal protein 72 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20221229 MGI PMID:36277211 1556870 Cep72 centrosomal protein 72 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20221229 MGI PMID:36277211 1556870 Cep72 centrosomal protein 72 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20221229 MGI PMID:36277211 1556870 Cep72 centrosomal protein 72 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20221229 MGI PMID:36277211 1556870 Cep72 centrosomal protein 72 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20221229 MGI PMID:36277211 1556870 Cep72 centrosomal protein 72 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20221229 MGI PMID:36277211 1556870 Cep72 centrosomal protein 72 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20221229 MGI PMID:36277211 1556870 Cep72 centrosomal protein 72 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20221229 MGI PMID:36277211 1556870 Cep72 centrosomal protein 72 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20221229 MGI PMID:36277211 1556870 Cep72 centrosomal protein 72 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20221229 MGI PMID:36277211 1556870 Cep72 centrosomal protein 72 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20221229 MGI PMID:36277211 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0008910 thin long bone epiphysis IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556873 Csgalnact2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20180308 MGI PMID:29287114 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20150212 MGI PMID:24306492 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0000445 short snout IEA N RGD:5509061 20141003 MGI 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0000644 dextrocardia IEA N RGD:5509061 20111116 MGI 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20141003 MGI 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:19906869 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20150212 MGI PMID:24306492 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0001947 abnormal mucociliary clearance IAGP N RGD:5509061 20141003 MGI PMID:19675306 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0001950 abnormal respiratory sounds IAGP N RGD:5509061 20141003 MGI PMID:20498047 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20150212 MGI PMID:24306492 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20150212 MGI PMID:24306492 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:19675306 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20191205 MGI PMID:26501274 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0002639 micrognathia IEA N RGD:5509061 20141003 MGI 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0003178 left pulmonary isomerism IEA N RGD:5509061 20141003 MGI 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:19906869 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20150212 MGI PMID:24306492 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20150212 MGI PMID:24306492 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20150212 MGI PMID:24306492 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0010463 aorta stenosis IEA N RGD:5509061 20141003 MGI 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20150212 MGI PMID:24306492 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0011249 abdominal situs inversus IEA N RGD:5509061 20141003 MGI 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0011250 abdominal situs ambiguus IEA N RGD:5509061 20111116 MGI 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0011251 bronchial situs inversus IEA N RGD:5509061 20111116 MGI 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0011252 situs inversus totalis IAGP N RGD:5509061 20150212 MGI PMID:24306492 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0011649 immotile respiratory cilia IEA N RGD:5509061 20141003 MGI 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20141003 MGI 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:19906869 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0013206 abnormal motile cilium morphology IAGP N RGD:5509061 20150212 MGI PMID:24306492 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0013209 abnormal motile cilium physiology IAGP N RGD:5509061 20150212 MGI PMID:24306492 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0030118 rhinosinusitis IAGP N RGD:5509061 20210211 MGI PMID:19675306 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0031088 coughing IAGP N RGD:5509061 20210211 MGI PMID:20498047 1556874 Dnai1 dynein axonemal intermediate chain 1 gene MP:0031089 sneezing IAGP N RGD:5509061 20210211 MGI PMID:20498047 1556875 Plin4 perilipin 4 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 1556875 Plin4 perilipin 4 gene MP:0001258 decreased body length IEA N RGD:5509061 20230601 MGI 1556875 Plin4 perilipin 4 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230601 MGI 1556875 Plin4 perilipin 4 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1556875 Plin4 perilipin 4 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1556875 Plin4 perilipin 4 gene MP:0031417 decreased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:23423172 1556876 Aig1 androgen-induced 1 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20210114 MGI PMID:32152231 1556876 Aig1 androgen-induced 1 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20210114 MGI PMID:32152231 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0000111 cleft palate IEA N RGD:5509061 20141003 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17452975 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20141003 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16459298 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20160616 MGI PMID:25760946 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0000433 microcephaly IEA N RGD:5509061 20141003 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20170105 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0000562 polydactyly IAGP N RGD:5509061 20160616 MGI PMID:25760946 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0000603 pale liver IEA N RGD:5509061 20210520 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20170105 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0000914 exencephaly IAGP N RGD:5509061 20160616 MGI PMID:25760946 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16459298 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16155214 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16459298 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:16459298 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0001488 increased startle reflex IEA N RGD:5509061 20201022 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16155214 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160114 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:16155214 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16155214 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16155214 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20074523 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0001785 edema IAGP N RGD:5509061 20160616 MGI PMID:25760946 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160616 MGI PMID:25760946 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16155214 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17452975 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16459298 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17452975 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:16155214 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20160811 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20160616 MGI PMID:25760946 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16459298 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20463034 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16155214 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0002639 micrognathia IEA N RGD:5509061 20141003 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:20074523 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:16459298 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0003641 small lung IAGP N RGD:5509061 20160616 MGI PMID:25760946 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:17452975 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:16459298 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16155214 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:16155214 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0004111 abnormal coronary artery morphology IEA N RGD:5509061 20141003 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20160616 MGI PMID:25760946 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:16155214 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20160114 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0004848 abnormal liver size IEA N RGD:5509061 20160811 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16155214 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20220519 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20160114 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:20074523 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:16459298 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17452975 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20074523 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20074523 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:20074523 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:20074523 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20170309 MGI PMID:16459298 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20141003 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20141003 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0010473 descending aorta dilation IAGP N RGD:5509061 20141003 MGI PMID:16155214 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0010476 coronary fistula IEA N RGD:5509061 20141003 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0010479 brain aneurysm IAGP N RGD:5509061 20141003 MGI PMID:16155214 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16155214 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16459298 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17452975 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20463034 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160616 MGI PMID:25760946 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20160616 MGI PMID:25760946 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160114 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0011495 abnormal head shape IEA N RGD:5509061 20141003 MGI 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17452975 1556878 Sufu SUFU negative regulator of hedgehog signaling gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20200820 MGI PMID:32704094 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11784869 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:11784869 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200820 MGI PMID:32704094 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0000603 pale liver IAGP N RGD:5509061 20200820 MGI PMID:32704094 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20200820 MGI PMID:32704094 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0001740 failure of adrenal epinephrine secretion IAGP N RGD:5509061 20141003 MGI PMID:11784869 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20200820 MGI PMID:32704094 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0002080 prenatal lethality IEA N RGD:5509061 20201231 MGI 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:11784869 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200820 MGI PMID:32704094 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:11784869 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20200820 MGI PMID:32704094 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20190502 MGI 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200820 MGI PMID:32704094 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11784869 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20200820 MGI PMID:32704094 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200820 MGI PMID:32704094 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20200820 MGI PMID:32704094 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0008247 abnormal mononuclear cell morphology IAGP N RGD:5509061 20200820 MGI PMID:32704094 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11784869 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11784869 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:11784869 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200820 MGI PMID:32704094 1556880 Ly6e lymphocyte antigen 6 family member E gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200820 MGI PMID:32704094 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16427009 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:16427009 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:16427009 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16427009 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:16427009 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16427009 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16427009 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:16427009 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16427009 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0003393 decreased cardiac output IEA N RGD:5509061 20240523 MGI 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:16427009 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:16427009 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:16427009 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:16427009 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20240523 MGI 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:16427009 1556882 Mdc1 mediator of DNA damage checkpoint 1 gene MP:0011952 decreased cardiac stroke volume IEA N RGD:5509061 20240523 MGI 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20160204 MGI PMID:24686385 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0000126 brittle teeth IAGP N RGD:5509061 20160204 MGI PMID:24686385 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20211014 MGI PMID:27283840 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20211014 MGI PMID:27283840 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0001868 ovary inflammation IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20160204 MGI PMID:24686385 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0002626 increased heart rate IAGP N RGD:5509061 20211014 MGI PMID:27283840 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20201022 MGI 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20160204 MGI PMID:24686385 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0004592 small mandible IAGP N RGD:5509061 20170921 MGI PMID:24686385 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20160204 MGI PMID:24686385 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20211014 MGI PMID:27283840 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20211014 MGI PMID:27283840 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0008837 increased transforming growth factor beta level IAGP N RGD:5509061 20211014 MGI PMID:27283840 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0009010 abnormal diestrus IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0009018 short estrus IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0009020 prolonged metestrus IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0011124 increased primary ovarian follicle number IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0011951 increased cardiac stroke volume IEA N RGD:5509061 20200402 MGI 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:24686385 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0021106 abnormal secondary ovarian follicle morphology IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0030080 small lower incisors IAGP N RGD:5509061 20170928 MGI PMID:24686385 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0030081 small upper incisors IAGP N RGD:5509061 20170928 MGI PMID:24686385 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0030089 short lower incisors IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0030090 short upper incisors IAGP N RGD:5509061 20220616 MGI PMID:34333627 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20180125 MGI PMID:24686385 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0030458 abnormal tooth wear IAGP N RGD:5509061 20180125 MGI PMID:24686385 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0031215 abnormal response to myocardial ischemic injury IAGP N RGD:5509061 20211014 MGI PMID:27283840 1556883 Grem2 gremlin 2, DAN family BMP antagonist gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:27283840 1556884 Il10rb interleukin 10 receptor, beta gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9463407 1556884 Il10rb interleukin 10 receptor, beta gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9463407 1556884 Il10rb interleukin 10 receptor, beta gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9463407 1556884 Il10rb interleukin 10 receptor, beta gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:9463407 1556884 Il10rb interleukin 10 receptor, beta gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9463407 1556884 Il10rb interleukin 10 receptor, beta gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9463407 1556884 Il10rb interleukin 10 receptor, beta gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18318596 1556884 Il10rb interleukin 10 receptor, beta gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18318596 1556884 Il10rb interleukin 10 receptor, beta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18318596 1556884 Il10rb interleukin 10 receptor, beta gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:18318596 1556884 Il10rb interleukin 10 receptor, beta gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:9463407 1556884 Il10rb interleukin 10 receptor, beta gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:18318596 1556884 Il10rb interleukin 10 receptor, beta gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:9463407 1556884 Il10rb interleukin 10 receptor, beta gene MP:0003305 proctitis IAGP N RGD:5509061 20141003 MGI PMID:18318596 1556884 Il10rb interleukin 10 receptor, beta gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:9463407 1556884 Il10rb interleukin 10 receptor, beta gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:18318596 1556884 Il10rb interleukin 10 receptor, beta gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:9463407 1556884 Il10rb interleukin 10 receptor, beta gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1556884 Il10rb interleukin 10 receptor, beta gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:9463407 1556884 Il10rb interleukin 10 receptor, beta gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:18318596 1556884 Il10rb interleukin 10 receptor, beta gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18318596 1556884 Il10rb interleukin 10 receptor, beta gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18318596 1556884 Il10rb interleukin 10 receptor, beta gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:18318596 1556884 Il10rb interleukin 10 receptor, beta gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18318596 1556884 Il10rb interleukin 10 receptor, beta gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:18318596 1556884 Il10rb interleukin 10 receptor, beta gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18318596 1556884 Il10rb interleukin 10 receptor, beta gene MP:0011224 abnormal lymph node medullary cord morphology IAGP N RGD:5509061 20141003 MGI PMID:9463407 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0000032 cochlear degeneration IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20170105 MGI 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0011968 decreased threshold for auditory brainstem response IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0020352 abnormal endoplasmic reticulum physiology IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556885 Tmtc4 transmembrane and tetratricopeptide repeat containing 4 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20190307 MGI PMID:30188326 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:22535952 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22535952 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:22535952 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001512 trunk curl IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22535952 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22535952 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:22535952 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22535952 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002338 abnormal pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0003382 straub tail IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20141003 MGI PMID:22535952 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0004142 abnormal muscle tone IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005114 premature hair loss IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:22535952 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005356 positive geotaxis IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005507 tail dragging IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:19460290 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005604 hyperekplexia IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0006051 brainstem hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20170309 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0009947 abnormal olfactory bulb external plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0009964 abnormal cerebellum lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0009983 abnormal cerebellum fastigial nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0010323 retropulsion IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0010746 abnormal pre-Botzinger complex physiology IAGP N RGD:5509061 20141003 MGI PMID:22653057 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:19460290 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:18396137 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:23702311 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:20534480 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0030655 increased circulating glycine level IAGP N RGD:5509061 20180920 MGI PMID:22535952 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0030670 increased circulating phenylalanine level IAGP N RGD:5509061 20180920 MGI PMID:22535952 1556886 Ndufs4 NADH:ubiquinone oxidoreductase core subunit S4 gene MP:0030745 increased circulating homocitrulline level IAGP N RGD:5509061 20240912 MGI PMID:22535952 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20230119 MGI 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:10917533 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0002219 decreased lymph node number IAGP N RGD:5509061 20141003 MGI PMID:10917533 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:10917533 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10917533 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12902460 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20230119 MGI 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:12902460 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:12902460 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20150702 MGI 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20230119 MGI 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:10917533 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:10917533 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0008201 absent follicular dendritic cells IAGP N RGD:5509061 20141003 MGI PMID:10917533 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10917533 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:10917533 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:10917533 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10917533 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0009628 absent brachial lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10917533 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10917533 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20240523 MGI 1556887 Cxcl13 C-X-C motif chemokine ligand 13 gene MP:0014472 impaired B cell migration IAGP N RGD:5509061 20240613 MGI PMID:17185562 1556888 Unkl unkempt family like zinc finger gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1556888 Unkl unkempt family like zinc finger gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1556889 Dock6 dedicator of cytokinesis 6 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1556889 Dock6 dedicator of cytokinesis 6 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1556889 Dock6 dedicator of cytokinesis 6 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20220811 MGI 1556889 Dock6 dedicator of cytokinesis 6 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1556890 Hoxc8 homeobox C8 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11311170 1556890 Hoxc8 homeobox C8 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:1348969 1556890 Hoxc8 homeobox C8 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:1348969 1556890 Hoxc8 homeobox C8 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:11311170 1556890 Hoxc8 homeobox C8 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:1348969 1556890 Hoxc8 homeobox C8 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:19621436 1556890 Hoxc8 homeobox C8 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:1348969 1556890 Hoxc8 homeobox C8 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:1348969 1556890 Hoxc8 homeobox C8 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:1348969 1556890 Hoxc8 homeobox C8 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:1348969 1556890 Hoxc8 homeobox C8 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:20510925 1556890 Hoxc8 homeobox C8 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11311170 1556890 Hoxc8 homeobox C8 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:1348969 1556890 Hoxc8 homeobox C8 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11311170 1556890 Hoxc8 homeobox C8 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:1348969 1556890 Hoxc8 homeobox C8 gene MP:0003807 camptodactyly IAGP N RGD:5509061 20141003 MGI PMID:1348969 1556890 Hoxc8 homeobox C8 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20141003 MGI PMID:11311170 1556890 Hoxc8 homeobox C8 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:19621436 1556890 Hoxc8 homeobox C8 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11311170 1556890 Hoxc8 homeobox C8 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11311170 1556890 Hoxc8 homeobox C8 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:11311170 1556890 Hoxc8 homeobox C8 gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:11311170 1556890 Hoxc8 homeobox C8 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:1348969 1556890 Hoxc8 homeobox C8 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:11311170 1556890 Hoxc8 homeobox C8 gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:20510925 1556890 Hoxc8 homeobox C8 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:11311170 1556890 Hoxc8 homeobox C8 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:1348969 1556890 Hoxc8 homeobox C8 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:19621436 1556890 Hoxc8 homeobox C8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1348969 1556890 Hoxc8 homeobox C8 gene MP:0012284 increased sternebra number IAGP N RGD:5509061 20141003 MGI PMID:11311170 1556891 Rusc1 RUN and SH3 domain containing 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20181227 MGI 1556891 Rusc1 RUN and SH3 domain containing 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1556891 Rusc1 RUN and SH3 domain containing 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 1556891 Rusc1 RUN and SH3 domain containing 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230601 MGI 1556891 Rusc1 RUN and SH3 domain containing 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220519 MGI 1556892 Rasgrp2 RAS, guanyl releasing protein 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20151217 MGI PMID:17492052 1556892 Rasgrp2 RAS, guanyl releasing protein 2 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:15334074 1556892 Rasgrp2 RAS, guanyl releasing protein 2 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:15334074 1556892 Rasgrp2 RAS, guanyl releasing protein 2 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20151217 MGI PMID:17492052 1556892 Rasgrp2 RAS, guanyl releasing protein 2 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:15334074 1556892 Rasgrp2 RAS, guanyl releasing protein 2 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20151217 MGI PMID:17492052 1556892 Rasgrp2 RAS, guanyl releasing protein 2 gene MP:0009676 abnormal hemostasis IAGP N RGD:5509061 20191212 MGI PMID:25705885 1556892 Rasgrp2 RAS, guanyl releasing protein 2 gene MP:0011898 abnormal platelet cell number IAGP N RGD:5509061 20191212 MGI PMID:25705885 1556894 Cd33 CD33 molecule gene MP:0001586 abnormal erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12773563 1556894 Cd33 CD33 molecule gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12773563 1556894 Cd33 CD33 molecule gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:12773563 1556894 Cd33 CD33 molecule gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20230119 MGI 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17374848 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17374848 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0001713 decreased trophoblast giant cell number IEA N RGD:5509061 20241010 MGI 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241010 MGI 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17374848 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17374848 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0003960 increased lean body mass IEA N RGD:5509061 20230119 MGI 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17374848 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0005505 thrombocytosis IEA N RGD:5509061 20230119 MGI 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17374848 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17374848 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20150212 MGI PMID:17374848 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20230119 MGI 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17374848 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0012706 decreased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17374848 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230119 MGI 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17374848 1556895 Rad54l2 RAD54 like 2 (S. cerevisiae) gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241010 MGI 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0003641 small lung IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0005039 hypoxia IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0009567 mitotic nondisjunction IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0010898 abnormal pulmonary alveolus epithelium morphology IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556899 Hnrnpa3 heterogeneous nuclear ribonucleoprotein A3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20201210 MGI PMID:32321712 1556901 Mrgprx1 MAS-related GPR, member X1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1556901 Mrgprx1 MAS-related GPR, member X1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20240530 MGI PMID:33358893 1556901 Mrgprx1 MAS-related GPR, member X1 gene MP:0010073 decreased pruritus IAGP N RGD:5509061 20240530 MGI PMID:33358893 1556902 Foxo4 forkhead box O4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1556902 Foxo4 forkhead box O4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1556902 Foxo4 forkhead box O4 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210520 MGI 1556902 Foxo4 forkhead box O4 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20150618 MGI PMID:25264246 1556902 Foxo4 forkhead box O4 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1556902 Foxo4 forkhead box O4 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 1556902 Foxo4 forkhead box O4 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 1556902 Foxo4 forkhead box O4 gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 1556902 Foxo4 forkhead box O4 gene MP:0002047 increased hepatic hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 1556902 Foxo4 forkhead box O4 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 1556902 Foxo4 forkhead box O4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20150618 MGI PMID:25264246 1556902 Foxo4 forkhead box O4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17254969 1556902 Foxo4 forkhead box O4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14978268 1556902 Foxo4 forkhead box O4 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20150618 MGI PMID:25264246 1556902 Foxo4 forkhead box O4 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 1556902 Foxo4 forkhead box O4 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20150618 MGI PMID:25264246 1556902 Foxo4 forkhead box O4 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20150618 MGI PMID:25264246 1556902 Foxo4 forkhead box O4 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 1556902 Foxo4 forkhead box O4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20150618 MGI PMID:25264246 1556902 Foxo4 forkhead box O4 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20150618 MGI PMID:25264246 1556902 Foxo4 forkhead box O4 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 1556902 Foxo4 forkhead box O4 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20150618 MGI PMID:25264246 1556902 Foxo4 forkhead box O4 gene MP:0009442 increased ovarian teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 1556902 Foxo4 forkhead box O4 gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 1556902 Foxo4 forkhead box O4 gene MP:0012437 increased Harderian gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 1556904 Tuba8 tubulin, alpha 8 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1556904 Tuba8 tubulin, alpha 8 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1556904 Tuba8 tubulin, alpha 8 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1556904 Tuba8 tubulin, alpha 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20171214 MGI PMID:28388629 1556904 Tuba8 tubulin, alpha 8 gene MP:0003929 decreased heart rate variability IEA N RGD:5509061 20231207 MGI 1556904 Tuba8 tubulin, alpha 8 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20231207 MGI 1556905 Prss36 serine protease 36 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1556907 Zfp28 zinc finger protein 28 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20240523 MGI 1556907 Zfp28 zinc finger protein 28 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20240523 MGI 1556910 Slc5a8 solute carrier family 5 (iodide transporter), member 8 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18562324 1556910 Slc5a8 solute carrier family 5 (iodide transporter), member 8 gene MP:0005310 abnormal salivary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:18562324 1556910 Slc5a8 solute carrier family 5 (iodide transporter), member 8 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18562324 1556911 Gpr146 G protein-coupled receptor 146 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210826 MGI 1556911 Gpr146 G protein-coupled receptor 146 gene MP:0000745 tremors IEA N RGD:5509061 20201231 MGI 1556911 Gpr146 G protein-coupled receptor 146 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 1556911 Gpr146 G protein-coupled receptor 146 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20200514 MGI 1556911 Gpr146 G protein-coupled receptor 146 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20201022 MGI 1556911 Gpr146 G protein-coupled receptor 146 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1556911 Gpr146 G protein-coupled receptor 146 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20210826 MGI 1556911 Gpr146 G protein-coupled receptor 146 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230601 MGI 1556911 Gpr146 G protein-coupled receptor 146 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200514 MGI 1556911 Gpr146 G protein-coupled receptor 146 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20201022 MGI 1556911 Gpr146 G protein-coupled receptor 146 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20201022 MGI 1556911 Gpr146 G protein-coupled receptor 146 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 1556911 Gpr146 G protein-coupled receptor 146 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 1556912 Cdyl chromodomain protein, Y chromosome-like gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20180329 MGI PMID:28076783 1556912 Cdyl chromodomain protein, Y chromosome-like gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20180329 MGI PMID:28076783 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:18703497 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:21038445 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0000126 brittle teeth IAGP N RGD:5509061 20171228 MGI PMID:18703497 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:21038445 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21038445 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15728677 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:18703497 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15728677 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:15728677 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0002649 abnormal enamel rod pattern IAGP N RGD:5509061 20141003 MGI PMID:18703497 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:18703497 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:21038445 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:15728677 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:21038445 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15728677 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0003932 abnormal molar crown morphology IAGP N RGD:5509061 20141003 MGI PMID:21038445 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0004830 short incisors IAGP N RGD:5509061 20141003 MGI PMID:18703497 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15728677 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0006402 small molars IAGP N RGD:5509061 20141003 MGI PMID:21038445 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:15728677 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0010096 abnormal incisor color IAGP N RGD:5509061 20141003 MGI PMID:18703497 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21038445 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0014165 absent ciliary process IAGP N RGD:5509061 20160414 MGI PMID:15728677 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0014175 abnormal ciliary epithelium morphology IAGP N RGD:5509061 20160505 MGI PMID:15728677 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:21038445 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0030138 abnormal lower incisor color IAGP N RGD:5509061 20171005 MGI PMID:21038445 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20171221 MGI PMID:18703497 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0030458 abnormal tooth wear IAGP N RGD:5509061 20171228 MGI PMID:18703497 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0030459 abnormal tooth attrition IAGP N RGD:5509061 20171228 MGI PMID:18703497 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0030500 conical molar IAGP N RGD:5509061 20180118 MGI PMID:21038445 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0030522 abnormal stellate reticulum morphology IAGP N RGD:5509061 20180118 MGI PMID:21038445 1556913 Nectin1 nectin cell adhesion molecule 1 gene MP:0030523 abnormal stratum intermedium morphology IAGP N RGD:5509061 20180118 MGI PMID:21038445 1556917 Atg9b autophagy related 9B gene MP:0001293 anophthalmia IEA N RGD:5509061 20181227 MGI 1556917 Atg9b autophagy related 9B gene MP:0001333 absent optic nerve IEA N RGD:5509061 20181227 MGI 1556917 Atg9b autophagy related 9B gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1556917 Atg9b autophagy related 9B gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1556918 Plekha2 pleckstrin homology domain-containing, family A (phosphoinositide binding specific) member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21204784 1556918 Plekha2 pleckstrin homology domain-containing, family A (phosphoinositide binding specific) member 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21204784 1556918 Plekha2 pleckstrin homology domain-containing, family A (phosphoinositide binding specific) member 2 gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:21204784 1556918 Plekha2 pleckstrin homology domain-containing, family A (phosphoinositide binding specific) member 2 gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:21204784 1556919 Atrnl1 attractin like 1 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:18064672 1556919 Atrnl1 attractin like 1 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:18064672 1556919 Atrnl1 attractin like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1556922 Pqbp1 polyglutamine binding protein 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20201210 MGI PMID:25070536 1556922 Pqbp1 polyglutamine binding protein 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20201210 MGI PMID:25070536 1556922 Pqbp1 polyglutamine binding protein 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20201210 MGI PMID:25070536 1556922 Pqbp1 polyglutamine binding protein 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20201210 MGI PMID:25070536 1556922 Pqbp1 polyglutamine binding protein 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1556922 Pqbp1 polyglutamine binding protein 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20201210 MGI PMID:25070536 1556922 Pqbp1 polyglutamine binding protein 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20201210 MGI PMID:25070536 1556922 Pqbp1 polyglutamine binding protein 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20201210 MGI PMID:25070536 1556922 Pqbp1 polyglutamine binding protein 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20201210 MGI PMID:25070536 1556922 Pqbp1 polyglutamine binding protein 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20201210 MGI PMID:25070536 1556922 Pqbp1 polyglutamine binding protein 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20201210 MGI PMID:25070536 1556922 Pqbp1 polyglutamine binding protein 1 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20201210 MGI PMID:25070536 1556922 Pqbp1 polyglutamine binding protein 1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20201210 MGI PMID:25070536 1556922 Pqbp1 polyglutamine binding protein 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20201210 MGI PMID:25070536 1556922 Pqbp1 polyglutamine binding protein 1 gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20201210 MGI PMID:25070536 1556924 H2-Ob histocompatibility 2, O region beta locus gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20180802 MGI PMID:10684291 1556924 H2-Ob histocompatibility 2, O region beta locus gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20180802 MGI PMID:12538662 1556924 H2-Ob histocompatibility 2, O region beta locus gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20180802 MGI PMID:10684291 1556924 H2-Ob histocompatibility 2, O region beta locus gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20180802 MGI PMID:12538662 1556924 H2-Ob histocompatibility 2, O region beta locus gene MP:0005043 defective assembly of class II molecules IAGP N RGD:5509061 20180809 MGI PMID:28813660 1556924 H2-Ob histocompatibility 2, O region beta locus gene MP:0020935 decreased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:18057254 1556924 H2-Ob histocompatibility 2, O region beta locus gene MP:0020935 decreased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:28813660 1556928 Oas1b 2'-5' oligoadenylate synthetase 1B gene MP:0020943 increased susceptibility to Flaviviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16589143 1556928 Oas1b 2'-5' oligoadenylate synthetase 1B gene MP:0020944 decreased susceptibility to Flaviviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16589143 1556928 Oas1b 2'-5' oligoadenylate synthetase 1B gene MP:0020944 decreased susceptibility to Flaviviridae infection IAGP N RGD:5509061 20200430 MGI PMID:17904183 1556928 Oas1b 2'-5' oligoadenylate synthetase 1B gene MP:0020944 decreased susceptibility to Flaviviridae infection IAGP N RGD:5509061 20200430 MGI PMID:8380081 1556931 Hoxb5 homeobox B5 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7828847 1556931 Hoxb5 homeobox B5 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:7828847 1556931 Hoxb5 homeobox B5 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:17626057 1556931 Hoxb5 homeobox B5 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1556931 Hoxb5 homeobox B5 gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:7828847 1556931 Hoxb5 homeobox B5 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:17626057 1556931 Hoxb5 homeobox B5 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1556931 Hoxb5 homeobox B5 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7828847 1556931 Hoxb5 homeobox B5 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:17626057 1556931 Hoxb5 homeobox B5 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1556931 Hoxb5 homeobox B5 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:17626057 1556931 Hoxb5 homeobox B5 gene MP:0004508 abnormal pectoral girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7828847 1556931 Hoxb5 homeobox B5 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1556931 Hoxb5 homeobox B5 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7828847 1556931 Hoxb5 homeobox B5 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1556931 Hoxb5 homeobox B5 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7828847 1556931 Hoxb5 homeobox B5 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:17626057 1556931 Hoxb5 homeobox B5 gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1556931 Hoxb5 homeobox B5 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1556931 Hoxb5 homeobox B5 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:17626057 1556931 Hoxb5 homeobox B5 gene MP:0012668 absent sternal manubrium IAGP N RGD:5509061 20141003 MGI PMID:17626057 1556934 Zdhhc9 zinc finger, DHHC domain containing 9 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20211021 MGI PMID:29944857 1556934 Zdhhc9 zinc finger, DHHC domain containing 9 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190711 MGI PMID:29944857 1556934 Zdhhc9 zinc finger, DHHC domain containing 9 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20190711 MGI PMID:29944857 1556934 Zdhhc9 zinc finger, DHHC domain containing 9 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20190711 MGI PMID:29944857 1556934 Zdhhc9 zinc finger, DHHC domain containing 9 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20211021 MGI PMID:26493479 1556934 Zdhhc9 zinc finger, DHHC domain containing 9 gene MP:0004144 hypotonia IAGP N RGD:5509061 20190711 MGI PMID:29944857 1556934 Zdhhc9 zinc finger, DHHC domain containing 9 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20211021 MGI PMID:26493479 1556934 Zdhhc9 zinc finger, DHHC domain containing 9 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20211021 MGI PMID:26493479 1556934 Zdhhc9 zinc finger, DHHC domain containing 9 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20211021 MGI PMID:26493479 1556934 Zdhhc9 zinc finger, DHHC domain containing 9 gene MP:0011995 decreased leukemia incidence IAGP N RGD:5509061 20211021 MGI PMID:26493479 1556934 Zdhhc9 zinc finger, DHHC domain containing 9 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20190711 MGI PMID:29944857 1556936 Oscar osteoclast associated receptor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21841309 1556936 Oscar osteoclast associated receptor gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:21841309 1556936 Oscar osteoclast associated receptor gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:21841309 1556936 Oscar osteoclast associated receptor gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:21841309 1556936 Oscar osteoclast associated receptor gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21841309 1556936 Oscar osteoclast associated receptor gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1556936 Oscar osteoclast associated receptor gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:21841309 1556936 Oscar osteoclast associated receptor gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:21841309 1556937 Polr1e polymerase (RNA) I polypeptide E gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1556937 Polr1e polymerase (RNA) I polypeptide E gene MP:0003345 decreased rib number IEA N RGD:5509061 20160804 MGI 1556937 Polr1e polymerase (RNA) I polypeptide E gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20160804 MGI 1556937 Polr1e polymerase (RNA) I polypeptide E gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1556937 Polr1e polymerase (RNA) I polypeptide E gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20160804 MGI 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20180719 MGI PMID:17761953 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20180719 MGI PMID:17761953 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20180719 MGI PMID:17761953 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20180719 MGI PMID:17761953 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:10982834 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20180719 MGI PMID:11457897 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20180719 MGI PMID:17761953 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20180719 MGI PMID:18792399 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180719 MGI PMID:17761953 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20180719 MGI PMID:17761953 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20180719 MGI PMID:11457897 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0005672 increased susceptibility to graft versus host disease IAGP N RGD:5509061 20180719 MGI PMID:18792399 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20180719 MGI PMID:17761953 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20180719 MGI PMID:17761953 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20180719 MGI PMID:17761953 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20180719 MGI PMID:17761953 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20180719 MGI PMID:11457897 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20180719 MGI PMID:17761953 1556938 Lilrb4a leukocyte immunoglobulin-like receptor, subfamily B, member 4A gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20180719 MGI PMID:17761953 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:19046572 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:21266327 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16962829 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19185849 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19185849 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19046572 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21266327 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:19185849 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16962829 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:17141160 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:16962829 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21266327 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22815285 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19185849 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21266327 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19046572 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:19046572 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19046572 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19046572 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:16962829 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22815285 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21266327 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:21266327 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21266327 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17141160 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:16962829 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:22815285 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:22815285 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22815285 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22815285 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21266327 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21266327 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22815285 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16962829 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:21266327 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0009734 abnormal prostate gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:19185849 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:19497867 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0010130 decreased DN1 thymic pro-T cell number IAGP N RGD:5509061 20141003 MGI PMID:22815285 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0010132 decreased DN2 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22815285 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0010134 decreased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22815285 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22815285 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16962829 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17043309 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17141160 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16962829 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16962829 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0011524 thick placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:17141160 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20150611 MGI PMID:21266327 1556939 Rictor RPTOR independent companion of MTOR, complex 2 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:19497867 1556940 Ces5a carboxylesterase 5A gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1556940 Ces5a carboxylesterase 5A gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1556940 Ces5a carboxylesterase 5A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210506 MGI PMID:32814578 1556940 Ces5a carboxylesterase 5A gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20210506 MGI PMID:32814578 1556940 Ces5a carboxylesterase 5A gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210506 MGI PMID:32814578 1556940 Ces5a carboxylesterase 5A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210506 MGI PMID:32814578 1556940 Ces5a carboxylesterase 5A gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1556940 Ces5a carboxylesterase 5A gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1556940 Ces5a carboxylesterase 5A gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230601 MGI 1556940 Ces5a carboxylesterase 5A gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210506 MGI PMID:32814578 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:1883968 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0000122 premature tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:1883968 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18371931 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:3712587 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0000914 exencephaly IEA N RGD:5509061 20111116 MGI 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:3712587 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:3712587 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:18371931 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:18371931 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:1883968 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:3712587 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0002082 postnatal lethality IEA N RGD:5509061 20111116 MGI 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:1883968 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:3712587 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:1883968 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18371931 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:1883968 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:1385849 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:1883968 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:3712587 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:8636651 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:1883968 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0003670 dilated renal glomerular capsule IAGP N RGD:5509061 20141003 MGI PMID:1883968 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12872122 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:1385849 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18371931 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:1883968 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:3712587 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:1883968 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:3712587 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0003985 renal fibrosis IEA N RGD:5509061 20111116 MGI 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:1385849 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:1883968 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:1385849 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:3712587 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:1385849 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:1883968 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:3712587 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0006084 abnormal circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:1385849 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:8636651 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20190725 MGI PMID:28205547 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0009051 dilated distal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:1883968 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0010052 increased grip strength IEA N RGD:5509061 20210520 MGI 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0010478 intracranial aneurysm IAGP N RGD:5509061 20141003 MGI PMID:1883968 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:18371931 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18371931 1556941 Nphp3 nephronophthisis 3 (adolescent) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1556942 Rnft2 ring finger protein, transmembrane 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1556943 Rpl39l ribosomal protein L39-like gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220210 MGI PMID:34825148 1556943 Rpl39l ribosomal protein L39-like gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220210 MGI PMID:34825148 1556943 Rpl39l ribosomal protein L39-like gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220210 MGI PMID:34825148 1556943 Rpl39l ribosomal protein L39-like gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20220210 MGI PMID:34825148 1556943 Rpl39l ribosomal protein L39-like gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220210 MGI PMID:34825148 1556943 Rpl39l ribosomal protein L39-like gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220210 MGI PMID:34825148 1556943 Rpl39l ribosomal protein L39-like gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20220210 MGI PMID:34825148 1556943 Rpl39l ribosomal protein L39-like gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220210 MGI PMID:34825148 1556943 Rpl39l ribosomal protein L39-like gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220210 MGI PMID:34825148 1556943 Rpl39l ribosomal protein L39-like gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20220210 MGI PMID:34825148 1556943 Rpl39l ribosomal protein L39-like gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220210 MGI PMID:34825148 1556943 Rpl39l ribosomal protein L39-like gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220210 MGI PMID:34825148 1556943 Rpl39l ribosomal protein L39-like gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220210 MGI PMID:34825148 1556943 Rpl39l ribosomal protein L39-like gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20220210 MGI PMID:34825148 1556943 Rpl39l ribosomal protein L39-like gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20220210 MGI PMID:34825148 1556946 Bdp1 B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20220519 MGI 1556946 Bdp1 B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1556946 Bdp1 B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20221215 MGI 1556946 Bdp1 B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1556946 Bdp1 B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210826 MGI 1556946 Bdp1 B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1556948 Helt helt bHLH transcription factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16968817 1556948 Helt helt bHLH transcription factor gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:16968817 1556948 Helt helt bHLH transcription factor gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16968817 1556948 Helt helt bHLH transcription factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16968817 1556948 Helt helt bHLH transcription factor gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16968817 1556948 Helt helt bHLH transcription factor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16968817 1556948 Helt helt bHLH transcription factor gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20141003 MGI PMID:16968817 1556948 Helt helt bHLH transcription factor gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20141003 MGI PMID:17611227 1556948 Helt helt bHLH transcription factor gene MP:0003247 abnormal glutaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17611227 1556948 Helt helt bHLH transcription factor gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:16968817 1556948 Helt helt bHLH transcription factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16968817 1556952 Leo1 Leo1, Paf1/RNA polymerase II complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160421 MGI 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20190103 MGI PMID:30372477 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20190103 MGI PMID:30372477 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20190103 MGI PMID:30372477 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20221103 MGI PMID:35238077 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0001337 dry eyes IAGP N RGD:5509061 20221103 MGI PMID:35238077 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20190103 MGI PMID:30372477 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0001994 increased blinking frequency IAGP N RGD:5509061 20221103 MGI PMID:35238077 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20190103 MGI PMID:30372477 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160421 MGI 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0005252 abnormal Meibomian gland morphology IAGP N RGD:5509061 20221103 MGI PMID:35238077 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20221103 MGI PMID:35238077 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0009535 abnormal skin sebaceous gland morphology IAGP N RGD:5509061 20190103 MGI PMID:30372477 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0012725 small sebaceous gland IAGP N RGD:5509061 20190103 MGI PMID:30372477 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0013376 abnormal sebocyte differentiation IAGP N RGD:5509061 20190103 MGI PMID:30372477 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0013391 abnormal Meibomian gland physiology IAGP N RGD:5509061 20221103 MGI PMID:35238077 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0014131 abnormal tear film morphology IAGP N RGD:5509061 20221103 MGI PMID:35238077 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0014132 abnormal tear film physiology IAGP N RGD:5509061 20221103 MGI PMID:35238077 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0020219 increased tear production IAGP N RGD:5509061 20221103 MGI PMID:35238077 1556953 Far2 fatty acyl CoA reductase 2 gene MP:0030572 abnormal pilosebaceous unit morphology IAGP N RGD:5509061 20190103 MGI PMID:30372477 1556954 Lrrc2 leucine rich repeat containing 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220519 MGI 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20170209 MGI PMID:27502165 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20210429 MGI PMID:25729399 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20170209 MGI PMID:27502165 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20160804 MGI 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20160804 MGI 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20220901 MGI PMID:32241915 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20220901 MGI PMID:32241915 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20170209 MGI PMID:27502165 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170209 MGI PMID:27502165 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20220901 MGI PMID:32241915 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160804 MGI 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20170209 MGI PMID:27502165 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20170209 MGI PMID:27502165 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20170209 MGI PMID:27502165 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0008191 abnormal follicular B cell physiology IAGP N RGD:5509061 20170209 MGI PMID:27502165 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20210429 MGI PMID:25729399 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20220901 MGI PMID:32241915 1556955 Dock10 dedicator of cytokinesis 10 gene MP:0010761 abnormal microglial cell chemotaxis IAGP N RGD:5509061 20220901 MGI PMID:32241915 1556958 Hira histone cell cycle regulator gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20141003 MGI 1556958 Hira histone cell cycle regulator gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20170216 MGI PMID:26935106 1556958 Hira histone cell cycle regulator gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170216 MGI PMID:26935106 1556958 Hira histone cell cycle regulator gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20170216 MGI PMID:26935106 1556958 Hira histone cell cycle regulator gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:19884347 1556958 Hira histone cell cycle regulator gene MP:0001684 abnormal axial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20170216 MGI PMID:26935106 1556958 Hira histone cell cycle regulator gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20170216 MGI PMID:26935106 1556958 Hira histone cell cycle regulator gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20170216 MGI PMID:26935106 1556958 Hira histone cell cycle regulator gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0003345 decreased rib number IEA N RGD:5509061 20160804 MGI 1556958 Hira histone cell cycle regulator gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20170216 MGI PMID:26935106 1556958 Hira histone cell cycle regulator gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0003674 oxidative stress IAGP N RGD:5509061 20170216 MGI PMID:26935106 1556958 Hira histone cell cycle regulator gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0004096 abnormal midbrain-hindbrain boundary development IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20170216 MGI PMID:26935106 1556958 Hira histone cell cycle regulator gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20170216 MGI PMID:26935106 1556958 Hira histone cell cycle regulator gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0004387 abnormal prechordal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20170216 MGI PMID:26935106 1556958 Hira histone cell cycle regulator gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20170216 MGI PMID:26935106 1556958 Hira histone cell cycle regulator gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19884347 1556958 Hira histone cell cycle regulator gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556958 Hira histone cell cycle regulator gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20170216 MGI PMID:26935106 1556958 Hira histone cell cycle regulator gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:11884616 1556960 Zfp609 zinc finger protein 609 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1556960 Zfp609 zinc finger protein 609 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200402 MGI 1556960 Zfp609 zinc finger protein 609 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1556960 Zfp609 zinc finger protein 609 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1556961 Nadsyn1 NAD synthetase 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200402 MGI 1556961 Nadsyn1 NAD synthetase 1 gene MP:0001314 cornea opacity IEA N RGD:5509061 20231207 MGI 1556961 Nadsyn1 NAD synthetase 1 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1556961 Nadsyn1 NAD synthetase 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1556961 Nadsyn1 NAD synthetase 1 gene MP:0005542 cornea vascularization IEA N RGD:5509061 20231207 MGI 1556961 Nadsyn1 NAD synthetase 1 gene MP:0005575 increased pulmonary ventilation IEA N RGD:5509061 20210128 MGI 1556961 Nadsyn1 NAD synthetase 1 gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20211021 MGI 1556961 Nadsyn1 NAD synthetase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 1556961 Nadsyn1 NAD synthetase 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1556961 Nadsyn1 NAD synthetase 1 gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20211021 MGI 1556965 Atg5 autophagy related 5 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:18701890 1556965 Atg5 autophagy related 5 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:23479732 1556965 Atg5 autophagy related 5 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17450150 1556965 Atg5 autophagy related 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:21493778 1556965 Atg5 autophagy related 5 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0002083 premature death IAGP N RGD:5509061 20180503 MGI PMID:29438013 1556965 Atg5 autophagy related 5 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17450150 1556965 Atg5 autophagy related 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9626506 1556965 Atg5 autophagy related 5 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18701890 1556965 Atg5 autophagy related 5 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20160728 MGI PMID:23615463 1556965 Atg5 autophagy related 5 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:17450150 1556965 Atg5 autophagy related 5 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17450150 1556965 Atg5 autophagy related 5 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20180503 MGI PMID:29438013 1556965 Atg5 autophagy related 5 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23479732 1556965 Atg5 autophagy related 5 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17450150 1556965 Atg5 autophagy related 5 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:20577052 1556965 Atg5 autophagy related 5 gene MP:0003143 enlarged otoliths IAGP N RGD:5509061 20141003 MGI PMID:20577052 1556965 Atg5 autophagy related 5 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20180503 MGI PMID:29438013 1556965 Atg5 autophagy related 5 gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:21493778 1556965 Atg5 autophagy related 5 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20230119 MGI PMID:35982178 1556965 Atg5 autophagy related 5 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20230119 MGI PMID:35982178 1556965 Atg5 autophagy related 5 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24185898 1556965 Atg5 autophagy related 5 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20160728 MGI PMID:23615463 1556965 Atg5 autophagy related 5 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:18701890 1556965 Atg5 autophagy related 5 gene MP:0003897 abnormal ST segment IAGP N RGD:5509061 20141003 MGI PMID:15525940 1556965 Atg5 autophagy related 5 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:21493778 1556965 Atg5 autophagy related 5 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20160728 MGI PMID:23615463 1556965 Atg5 autophagy related 5 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:17450150 1556965 Atg5 autophagy related 5 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:17450150 1556965 Atg5 autophagy related 5 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21493778 1556965 Atg5 autophagy related 5 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18849966 1556965 Atg5 autophagy related 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20160728 MGI PMID:23615463 1556965 Atg5 autophagy related 5 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:15525940 1556965 Atg5 autophagy related 5 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20160728 MGI PMID:23615463 1556965 Atg5 autophagy related 5 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20180503 MGI PMID:29438013 1556965 Atg5 autophagy related 5 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:15525940 1556965 Atg5 autophagy related 5 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:15525940 1556965 Atg5 autophagy related 5 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24209762 1556965 Atg5 autophagy related 5 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:17450150 1556965 Atg5 autophagy related 5 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20577052 1556965 Atg5 autophagy related 5 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:17450150 1556965 Atg5 autophagy related 5 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20160728 MGI PMID:23615463 1556965 Atg5 autophagy related 5 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20160728 MGI PMID:23615463 1556965 Atg5 autophagy related 5 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20160728 MGI PMID:23615463 1556965 Atg5 autophagy related 5 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:23870125 1556965 Atg5 autophagy related 5 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20160811 MGI PMID:25585051 1556965 Atg5 autophagy related 5 gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17450150 1556965 Atg5 autophagy related 5 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:15525940 1556965 Atg5 autophagy related 5 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17450150 1556965 Atg5 autophagy related 5 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200917 MGI PMID:30874544 1556965 Atg5 autophagy related 5 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0009837 abnormal sperm end piece morphology IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0009974 decreased cerebral cortex pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16625204 1556965 Atg5 autophagy related 5 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1556965 Atg5 autophagy related 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23426372 1556965 Atg5 autophagy related 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15525940 1556965 Atg5 autophagy related 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18701890 1556965 Atg5 autophagy related 5 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20160728 MGI PMID:23615463 1556965 Atg5 autophagy related 5 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20141003 MGI PMID:23870125 1556965 Atg5 autophagy related 5 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20141003 MGI PMID:23870125 1556965 Atg5 autophagy related 5 gene MP:0020406 hyperthreoninuria IAGP N RGD:5509061 20161208 MGI PMID:21493778 1556965 Atg5 autophagy related 5 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0030591 absent sperm fibrous sheath IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0030618 tryptophanuria IAGP N RGD:5509061 20180906 MGI PMID:21493778 1556965 Atg5 autophagy related 5 gene MP:0030620 valinuria IAGP N RGD:5509061 20180920 MGI PMID:21493778 1556965 Atg5 autophagy related 5 gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20190711 MGI PMID:18701890 1556965 Atg5 autophagy related 5 gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20190711 MGI PMID:29438013 1556965 Atg5 autophagy related 5 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:18849966 1556965 Atg5 autophagy related 5 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:21493778 1556965 Atg5 autophagy related 5 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:23479732 1556965 Atg5 autophagy related 5 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:23615463 1556965 Atg5 autophagy related 5 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220310 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0031372 abnormal sperm individualization IAGP N RGD:5509061 20220331 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0031409 double-headed sperm IAGP N RGD:5509061 20220630 MGI PMID:32677505 1556965 Atg5 autophagy related 5 gene MP:0031641 alaninuria IAGP N RGD:5509061 20240801 MGI PMID:21493778 1556966 Vmn1r51 vomeronasal 1 receptor 51 gene MP:0009945 abnormal accessory olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:11222144 1556967 St6gal2 beta galactoside alpha 2,6 sialyltransferase 2 gene MP:0004357 long tibia IEA N RGD:5509061 20211021 MGI 1556967 St6gal2 beta galactoside alpha 2,6 sialyltransferase 2 gene MP:0009455 enhanced cued conditioning behavior IEA N RGD:5509061 20230601 MGI 1556968 Jade3 jade family PHD finger 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1556969 Astl astacin like metalloendopeptidase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:22206759 1556969 Astl astacin like metalloendopeptidase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:22472438 1556969 Astl astacin like metalloendopeptidase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:22472438 1556970 Mpp3 membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3) gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23658188 1556970 Mpp3 membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3) gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23893895 1556970 Mpp3 membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3) gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:23893895 1556970 Mpp3 membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3) gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20231207 MGI 1556970 Mpp3 membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3) gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23893895 1556970 Mpp3 membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3) gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23893895 1556970 Mpp3 membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3) gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20231207 MGI 1556970 Mpp3 membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3) gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:23658188 1556970 Mpp3 membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3) gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1556970 Mpp3 membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3) gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20231207 MGI 1556970 Mpp3 membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3) gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:23658188 1556970 Mpp3 membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3) gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:23658188 1556970 Mpp3 membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3) gene MP:0010236 abnormal retina outer limiting membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:23893895 1556970 Mpp3 membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3) gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20141003 MGI PMID:23893895 1556970 Mpp3 membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3) gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:23893895 1556971 Zfp74 zinc finger protein 74 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230119 MGI 1556971 Zfp74 zinc finger protein 74 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230119 MGI 1556972 Jmy junction-mediating and regulatory protein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210805 MGI PMID:32279424 1556972 Jmy junction-mediating and regulatory protein gene MP:0001935 decreased litter size IAGP N RGD:5509061 20210805 MGI PMID:32279424 1556972 Jmy junction-mediating and regulatory protein gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20210805 MGI PMID:32279424 1556972 Jmy junction-mediating and regulatory protein gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210805 MGI PMID:32279424 1556972 Jmy junction-mediating and regulatory protein gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210805 MGI PMID:32279424 1556972 Jmy junction-mediating and regulatory protein gene MP:0009233 enlarged sperm head IAGP N RGD:5509061 20210805 MGI PMID:32279424 1556972 Jmy junction-mediating and regulatory protein gene MP:0020356 abnormal Sertoli cell barrier function IAGP N RGD:5509061 20210805 MGI PMID:32279424 1556972 Jmy junction-mediating and regulatory protein gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210805 MGI PMID:32279424 1556974 Mroh9 maestro heat-like repeat family member 9 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1556979 Cntd1 cyclin N-terminal domain containing 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1556979 Cntd1 cyclin N-terminal domain containing 1 gene MP:0001147 small testis IAGP N RGD:5509061 20180705 MGI PMID:24891606 1556979 Cntd1 cyclin N-terminal domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20180705 MGI PMID:24891606 1556979 Cntd1 cyclin N-terminal domain containing 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20180705 MGI PMID:24891606 1556979 Cntd1 cyclin N-terminal domain containing 1 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20201001 MGI PMID:32555348 1556979 Cntd1 cyclin N-terminal domain containing 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20180705 MGI PMID:24891606 1556979 Cntd1 cyclin N-terminal domain containing 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20180705 MGI PMID:24891606 1556979 Cntd1 cyclin N-terminal domain containing 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20180705 MGI PMID:24891606 1556979 Cntd1 cyclin N-terminal domain containing 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20180705 MGI PMID:24891606 1556979 Cntd1 cyclin N-terminal domain containing 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20180705 MGI PMID:24891606 1556980 Pcdh9 protocadherin 9 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220428 MGI 1556980 Pcdh9 protocadherin 9 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170314 MGI PMID:25802080 1556980 Pcdh9 protocadherin 9 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1556980 Pcdh9 protocadherin 9 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20170314 MGI PMID:25802080 1556980 Pcdh9 protocadherin 9 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20181227 MGI 1556980 Pcdh9 protocadherin 9 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1556980 Pcdh9 protocadherin 9 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1556980 Pcdh9 protocadherin 9 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20170314 MGI PMID:25802080 1556980 Pcdh9 protocadherin 9 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20170314 MGI PMID:25802080 1556980 Pcdh9 protocadherin 9 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20170314 MGI PMID:25802080 1556980 Pcdh9 protocadherin 9 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20170314 MGI PMID:25802080 1556980 Pcdh9 protocadherin 9 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1556980 Pcdh9 protocadherin 9 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1556980 Pcdh9 protocadherin 9 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:25802080 1556980 Pcdh9 protocadherin 9 gene MP:0020396 abnormal social recognition IAGP N RGD:5509061 20170314 MGI PMID:25802080 1556980 Pcdh9 protocadherin 9 gene MP:0021019 increased dendritic spine number IAGP N RGD:5509061 20211014 MGI PMID:25802080 1556980 Pcdh9 protocadherin 9 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:25802080 1556981 Cd27 CD27 antigen gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15723067 1556981 Cd27 CD27 antigen gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1556981 Cd27 CD27 antigen gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1556981 Cd27 CD27 antigen gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1556981 Cd27 CD27 antigen gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1556981 Cd27 CD27 antigen gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1556981 Cd27 CD27 antigen gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20230601 MGI 1556981 Cd27 CD27 antigen gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1556981 Cd27 CD27 antigen gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11062504 1556981 Cd27 CD27 antigen gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1556981 Cd27 CD27 antigen gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230601 MGI 1556981 Cd27 CD27 antigen gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23547099 1556981 Cd27 CD27 antigen gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11062504 1556981 Cd27 CD27 antigen gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15723067 1556981 Cd27 CD27 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11062504 1556981 Cd27 CD27 antigen gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23547099 1556981 Cd27 CD27 antigen gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1556981 Cd27 CD27 antigen gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20230601 MGI 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0000066 osteoporosis IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0008638 increased circulating interleukin-1 alpha level IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0030439 decreased osteoblast proliferation IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0030985 decreased circulating osteocalcin level IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556984 Itln1 intelectin 1 (galactofuranose binding) gene MP:0031074 increased circulating type I collagen C-terminal telopeptide level IAGP N RGD:5509061 20201210 MGI PMID:29619269 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0000162 lordosis IAGP N RGD:5509061 20151126 MGI PMID:3711636 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0000396 increased curvature of hairs IAGP N RGD:5509061 20141003 MGI PMID:22496784 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20141003 MGI PMID:22496784 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:22496784 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0000410 waved hair IAGP N RGD:5509061 20151126 MGI PMID:3711636 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0001177 atelectasis IAGP N RGD:5509061 20151126 MGI PMID:3711636 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:22496784 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0001280 loss of vibrissae IAGP N RGD:5509061 20141003 MGI PMID:22496784 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0001406 abnormal gait IAGP N RGD:5509061 20151126 MGI PMID:3711636 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20151126 MGI PMID:3711636 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20151126 MGI PMID:3711636 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20141003 MGI PMID:22496784 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:22496784 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20151126 MGI PMID:3711636 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170105 MGI 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:23884312 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0003109 short femur IAGP N RGD:5509061 20151126 MGI PMID:3711636 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0003641 small lung IAGP N RGD:5509061 20151126 MGI PMID:3711636 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:22496784 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20141003 MGI PMID:22496784 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0003848 brittle hair IAGP N RGD:5509061 20141003 MGI PMID:22496784 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20151126 MGI PMID:3711636 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:22496784 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0008538 decreased zigzag hair amount IAGP N RGD:5509061 20141003 MGI PMID:22496784 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0009351 thin hair shaft IEA N RGD:5509061 20151126 MGI 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0009441 delayed skin barrier formation IAGP N RGD:5509061 20141003 MGI PMID:22496784 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0009801 abnormal hair cortex keratinization IAGP N RGD:5509061 20141003 MGI PMID:22496784 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20151126 MGI PMID:3711636 1556985 Tgm3 transglutaminase 3, E polypeptide gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20151126 MGI PMID:3711636 1556988 Padi6 peptidyl arginine deiminase, type VI gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17587491 1556988 Padi6 peptidyl arginine deiminase, type VI gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18599511 1556988 Padi6 peptidyl arginine deiminase, type VI gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18599511 1556988 Padi6 peptidyl arginine deiminase, type VI gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17587491 1556988 Padi6 peptidyl arginine deiminase, type VI gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:17587491 1556992 Gjb4 gap junction protein, beta 4 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20181227 MGI 1556992 Gjb4 gap junction protein, beta 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 1556992 Gjb4 gap junction protein, beta 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20181227 MGI 1556992 Gjb4 gap junction protein, beta 4 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1556992 Gjb4 gap junction protein, beta 4 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210520 MGI 1556992 Gjb4 gap junction protein, beta 4 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:17728008 1556992 Gjb4 gap junction protein, beta 4 gene MP:0009709 hydrometra IEA N RGD:5509061 20170105 MGI 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0001967 deafness IAGP N RGD:5509061 20161110 MGI PMID:26662512 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0001967 deafness IAGP N RGD:5509061 20180712 MGI PMID:27660326 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20150129 MGI PMID:24135232 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:18084280 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20161110 MGI PMID:26662512 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20150129 MGI PMID:24135232 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20180712 MGI PMID:27660326 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20161110 MGI PMID:26662512 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20161110 MGI PMID:26662512 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0004536 short inner hair cell stereocilia IAGP N RGD:5509061 20161110 MGI PMID:26662512 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18084280 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20161110 MGI PMID:26662512 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20161110 MGI PMID:26662512 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0011060 abnormal kinocilium morphology IAGP N RGD:5509061 20150129 MGI PMID:24135232 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20161110 MGI PMID:26662512 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20180712 MGI PMID:27660326 1556993 Gpsm2 G-protein signalling modulator 2 (AGS3-like, C. elegans) gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20161013 MGI PMID:24135232 1556994 Sp6 trans-acting transcription factor 6 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:18156176 1556994 Sp6 trans-acting transcription factor 6 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0000126 brittle teeth IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0000387 disorganized inner root sheath cells IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18156176 1556994 Sp6 trans-acting transcription factor 6 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18156176 1556994 Sp6 trans-acting transcription factor 6 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0002817 abnormal tooth mineralization IAGP N RGD:5509061 20141003 MGI PMID:18156176 1556994 Sp6 trans-acting transcription factor 6 gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20141003 MGI PMID:18156176 1556994 Sp6 trans-acting transcription factor 6 gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0003053 delayed tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:18156176 1556994 Sp6 trans-acting transcription factor 6 gene MP:0003404 absent enamel IAGP N RGD:5509061 20141003 MGI PMID:18156176 1556994 Sp6 trans-acting transcription factor 6 gene MP:0003404 absent enamel IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0003930 abnormal tooth hard tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20141003 MGI PMID:18156176 1556994 Sp6 trans-acting transcription factor 6 gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20171228 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0006369 supernumerary incisors IAGP N RGD:5509061 20141003 MGI PMID:18156176 1556994 Sp6 trans-acting transcription factor 6 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18156176 1556994 Sp6 trans-acting transcription factor 6 gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0010747 abnormal enamel organ morphology IAGP N RGD:5509061 20171221 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0010773 supernumerary molars IAGP N RGD:5509061 20171228 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0013129 abnormal tooth color IAGP N RGD:5509061 20171221 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0030079 small incisors IAGP N RGD:5509061 20171228 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0030088 microdontia IAGP N RGD:5509061 20171228 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20171221 MGI PMID:18156176 1556994 Sp6 trans-acting transcription factor 6 gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20171221 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0030472 fused teeth IAGP N RGD:5509061 20171228 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0030473 fused molars IAGP N RGD:5509061 20171228 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0030497 short tooth root IAGP N RGD:5509061 20171228 MGI PMID:18297738 1556994 Sp6 trans-acting transcription factor 6 gene MP:0030525 abnormal Hertwig epithelial root sheath morphology IAGP N RGD:5509061 20180118 MGI PMID:18297738 1556995 Serpinb9 serine (or cysteine) peptidase inhibitor, clade B, member 9 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20180118 MGI PMID:22801574 1556995 Serpinb9 serine (or cysteine) peptidase inhibitor, clade B, member 9 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20180118 MGI PMID:22801574 1556995 Serpinb9 serine (or cysteine) peptidase inhibitor, clade B, member 9 gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16618603 1556995 Serpinb9 serine (or cysteine) peptidase inhibitor, clade B, member 9 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20180118 MGI PMID:22801574 1556995 Serpinb9 serine (or cysteine) peptidase inhibitor, clade B, member 9 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16618603 1556995 Serpinb9 serine (or cysteine) peptidase inhibitor, clade B, member 9 gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:16618603 1556995 Serpinb9 serine (or cysteine) peptidase inhibitor, clade B, member 9 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:16618603 1556995 Serpinb9 serine (or cysteine) peptidase inhibitor, clade B, member 9 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16618603 1556995 Serpinb9 serine (or cysteine) peptidase inhibitor, clade B, member 9 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:16618603 1556995 Serpinb9 serine (or cysteine) peptidase inhibitor, clade B, member 9 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16618603 1556995 Serpinb9 serine (or cysteine) peptidase inhibitor, clade B, member 9 gene MP:0012191 decreased cytotoxic T cell apoptosis IAGP N RGD:5509061 20180118 MGI PMID:22801574 1556995 Serpinb9 serine (or cysteine) peptidase inhibitor, clade B, member 9 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:16618603 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20210617 MGI PMID:25376646 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20210617 MGI PMID:25376646 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0000692 small spleen IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0001891 hydrocephaly IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20210617 MGI PMID:25376646 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0002282 abnormal trachea morphology IEA N RGD:5509061 20210520 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0002834 decreased heart weight IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20210617 MGI PMID:25376646 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20231207 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0010875 increased bone volume IAGP N RGD:5509061 20210617 MGI PMID:25376646 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20210617 MGI PMID:25376646 1556999 Naa10 N(alpha)-acetyltransferase 10, NatA catalytic subunit gene MP:0030278 thick neurocranium IAGP N RGD:5509061 20210617 MGI PMID:25376646 1557001 Tpm2 tropomyosin 2, beta gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20191114 MGI PMID:29510160 1557001 Tpm2 tropomyosin 2, beta gene MP:0001304 cataract IAGP N RGD:5509061 20191114 MGI PMID:29510160 1557001 Tpm2 tropomyosin 2, beta gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20191114 MGI PMID:29510160 1557001 Tpm2 tropomyosin 2, beta gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20191114 MGI PMID:29510160 1557001 Tpm2 tropomyosin 2, beta gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20191114 MGI PMID:29510160 1557003 Nsun3 NOL1/NOP2/Sun domain family member 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20241003 MGI PMID:36949224 1557003 Nsun3 NOL1/NOP2/Sun domain family member 3 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20241003 MGI PMID:36949224 1557003 Nsun3 NOL1/NOP2/Sun domain family member 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20241003 MGI PMID:36949224 1557003 Nsun3 NOL1/NOP2/Sun domain family member 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20241003 MGI PMID:36949224 1557003 Nsun3 NOL1/NOP2/Sun domain family member 3 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20241003 MGI PMID:36949224 1557003 Nsun3 NOL1/NOP2/Sun domain family member 3 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20241003 MGI PMID:36949224 1557003 Nsun3 NOL1/NOP2/Sun domain family member 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20241003 MGI PMID:36949224 1557003 Nsun3 NOL1/NOP2/Sun domain family member 3 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20241003 MGI PMID:36949224 1557003 Nsun3 NOL1/NOP2/Sun domain family member 3 gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20241003 MGI PMID:36949224 1557004 Egfl6 EGF-like-domain, multiple 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22613833 1557004 Egfl6 EGF-like-domain, multiple 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200723 MGI PMID:32231122 1557005 Frmd5 FERM domain containing 5 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1557005 Frmd5 FERM domain containing 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 1557005 Frmd5 FERM domain containing 5 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20240328 MGI PMID:38228891 1557005 Frmd5 FERM domain containing 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20240328 MGI PMID:38228891 1557005 Frmd5 FERM domain containing 5 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20240328 MGI PMID:38228891 1557005 Frmd5 FERM domain containing 5 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20240328 MGI PMID:38228891 1557005 Frmd5 FERM domain containing 5 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20240328 MGI PMID:38228891 1557005 Frmd5 FERM domain containing 5 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20240328 MGI PMID:38228891 1557005 Frmd5 FERM domain containing 5 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20240328 MGI PMID:38228891 1557005 Frmd5 FERM domain containing 5 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20160804 MGI 1557005 Frmd5 FERM domain containing 5 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160804 MGI 1557005 Frmd5 FERM domain containing 5 gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:38228891 1557005 Frmd5 FERM domain containing 5 gene MP:0020511 decreased dendritic spine length IAGP N RGD:5509061 20240328 MGI PMID:38228891 1557005 Frmd5 FERM domain containing 5 gene MP:0020512 abnormal dendritic mushroom spine morphology IAGP N RGD:5509061 20240328 MGI PMID:38228891 1557005 Frmd5 FERM domain containing 5 gene MP:0020513 abnormal dendritic stubby spine morphology IAGP N RGD:5509061 20240328 MGI PMID:38228891 1557005 Frmd5 FERM domain containing 5 gene MP:0020514 abnormal dendritic thin spine morphology IAGP N RGD:5509061 20240328 MGI PMID:38228891 1557005 Frmd5 FERM domain containing 5 gene MP:0021090 abnormal dendrite arborization pattern IAGP N RGD:5509061 20240328 MGI PMID:38228891 1557005 Frmd5 FERM domain containing 5 gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20240328 MGI PMID:38228891 1557005 Frmd5 FERM domain containing 5 gene MP:0021112 impaired social recognition IAGP N RGD:5509061 20240328 MGI PMID:38228891 1557007 Ociad2 OCIA domain containing 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1557007 Ociad2 OCIA domain containing 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1557007 Ociad2 OCIA domain containing 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0020423 abnormal mitochondrial biogenesis IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557008 Rangrf RAN guanine nucleotide release factor gene MP:0030567 abnormal I band morphology IAGP N RGD:5509061 20221215 MGI PMID:35533905 1557009 Glis3 GLIS family zinc finger 3 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:19481545 1557009 Glis3 GLIS family zinc finger 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19273592 1557009 Glis3 GLIS family zinc finger 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19481545 1557009 Glis3 GLIS family zinc finger 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19273592 1557009 Glis3 GLIS family zinc finger 3 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:19481545 1557009 Glis3 GLIS family zinc finger 3 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:19273592 1557009 Glis3 GLIS family zinc finger 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:19481545 1557009 Glis3 GLIS family zinc finger 3 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:19481545 1557009 Glis3 GLIS family zinc finger 3 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:19481545 1557009 Glis3 GLIS family zinc finger 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19481545 1557009 Glis3 GLIS family zinc finger 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19481545 1557009 Glis3 GLIS family zinc finger 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:19273592 1557009 Glis3 GLIS family zinc finger 3 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:19481545 1557009 Glis3 GLIS family zinc finger 3 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19481545 1557009 Glis3 GLIS family zinc finger 3 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0009174 absent pancreatic beta cells IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:19481545 1557009 Glis3 GLIS family zinc finger 3 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0009178 absent pancreatic alpha cells IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0009181 decreased pancreatic delta cell number IAGP N RGD:5509061 20141003 MGI PMID:19481545 1557009 Glis3 GLIS family zinc finger 3 gene MP:0009181 decreased pancreatic delta cell number IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0009191 decreased pancreatic epsilon cell number IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:19273592 1557009 Glis3 GLIS family zinc finger 3 gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:19273592 1557009 Glis3 GLIS family zinc finger 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19273592 1557009 Glis3 GLIS family zinc finger 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19481545 1557009 Glis3 GLIS family zinc finger 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21786021 1557009 Glis3 GLIS family zinc finger 3 gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:19273592 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16234806 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16234806 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22117778 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16234806 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16234806 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:16234806 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20141003 MGI PMID:16234806 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20537373 1557010 Cbln1 cerebellin 1 precursor protein gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:16234806 1557013 Fgf6 fibroblast growth factor 6 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:9284044 1557013 Fgf6 fibroblast growth factor 6 gene MP:0000730 increased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:9284044 1557013 Fgf6 fibroblast growth factor 6 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:9284044 1557013 Fgf6 fibroblast growth factor 6 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:12917328 1557013 Fgf6 fibroblast growth factor 6 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12917328 1557013 Fgf6 fibroblast growth factor 6 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9284044 1557013 Fgf6 fibroblast growth factor 6 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:12917328 1557013 Fgf6 fibroblast growth factor 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9303352 1557013 Fgf6 fibroblast growth factor 6 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:9284044 1557013 Fgf6 fibroblast growth factor 6 gene MP:0002881 long hair IAGP N RGD:5509061 20141003 MGI PMID:12917328 1557013 Fgf6 fibroblast growth factor 6 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12917328 1557013 Fgf6 fibroblast growth factor 6 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:12917328 1557013 Fgf6 fibroblast growth factor 6 gene MP:0003358 abnormal hypaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9284044 1557013 Fgf6 fibroblast growth factor 6 gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:12917328 1557013 Fgf6 fibroblast growth factor 6 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:12917328 1557013 Fgf6 fibroblast growth factor 6 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:9284044 1557013 Fgf6 fibroblast growth factor 6 gene MP:0004248 abnormal epaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9284044 1557013 Fgf6 fibroblast growth factor 6 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:12917328 1557013 Fgf6 fibroblast growth factor 6 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:12917328 1557013 Fgf6 fibroblast growth factor 6 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:9284044 1557013 Fgf6 fibroblast growth factor 6 gene MP:0030945 abnormal myoblast migration IAGP N RGD:5509061 20211125 MGI PMID:12917328 1557014 Plin5 perilipin 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20210930 MGI PMID:27376234 1557014 Plin5 perilipin 5 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20210930 MGI PMID:27376234 1557014 Plin5 perilipin 5 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22532565 1557014 Plin5 perilipin 5 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20210930 MGI PMID:27376234 1557014 Plin5 perilipin 5 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:22532565 1557014 Plin5 perilipin 5 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22532565 1557014 Plin5 perilipin 5 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20170720 MGI PMID:25161888 1557014 Plin5 perilipin 5 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22532565 1557014 Plin5 perilipin 5 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20210930 MGI PMID:27376234 1557014 Plin5 perilipin 5 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22532565 1557014 Plin5 perilipin 5 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20210930 MGI PMID:27376234 1557014 Plin5 perilipin 5 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22532565 1557014 Plin5 perilipin 5 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22532565 1557014 Plin5 perilipin 5 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20170720 MGI PMID:25161888 1557014 Plin5 perilipin 5 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:22532565 1557014 Plin5 perilipin 5 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22532565 1557014 Plin5 perilipin 5 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20170720 MGI PMID:25161888 1557014 Plin5 perilipin 5 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20170720 MGI PMID:25161888 1557014 Plin5 perilipin 5 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22532565 1557014 Plin5 perilipin 5 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22532565 1557014 Plin5 perilipin 5 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210930 MGI PMID:27376234 1557014 Plin5 perilipin 5 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20170720 MGI PMID:25161888 1557014 Plin5 perilipin 5 gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22532565 1557014 Plin5 perilipin 5 gene MP:0010360 decreased liver free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22532565 1557014 Plin5 perilipin 5 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20170720 MGI PMID:25161888 1557014 Plin5 perilipin 5 gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20170720 MGI PMID:25161888 1557014 Plin5 perilipin 5 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20170720 MGI PMID:25161888 1557014 Plin5 perilipin 5 gene MP:0013243 abnormal carbohydrate metabolism IAGP N RGD:5509061 20170720 MGI PMID:25161888 1557014 Plin5 perilipin 5 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:22532565 1557014 Plin5 perilipin 5 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20170720 MGI PMID:25161888 1557014 Plin5 perilipin 5 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20170720 MGI PMID:25161888 1557014 Plin5 perilipin 5 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20210930 MGI PMID:27376234 1557014 Plin5 perilipin 5 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:25161888 1557014 Plin5 perilipin 5 gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20210930 MGI PMID:27376234 1557014 Plin5 perilipin 5 gene MP:0031414 decreased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:25161888 1557014 Plin5 perilipin 5 gene MP:0031417 decreased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:22532565 1557014 Plin5 perilipin 5 gene MP:0031417 decreased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:25161888 1557014 Plin5 perilipin 5 gene MP:0031417 decreased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:27376234 1557015 Zmym3 zinc finger, MYM-type 3 gene MP:0001147 small testis IAGP N RGD:5509061 20220630 MGI PMID:28661483 1557015 Zmym3 zinc finger, MYM-type 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220630 MGI PMID:28661483 1557015 Zmym3 zinc finger, MYM-type 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20220630 MGI PMID:28661483 1557015 Zmym3 zinc finger, MYM-type 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220630 MGI PMID:28661483 1557015 Zmym3 zinc finger, MYM-type 3 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20220630 MGI PMID:28661483 1557015 Zmym3 zinc finger, MYM-type 3 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220630 MGI PMID:28661483 1557015 Zmym3 zinc finger, MYM-type 3 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20220630 MGI PMID:28661483 1557015 Zmym3 zinc finger, MYM-type 3 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220630 MGI PMID:28661483 1557016 Pigf phosphatidylinositol glycan anchor biosynthesis, class F gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1557016 Pigf phosphatidylinositol glycan anchor biosynthesis, class F gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1557016 Pigf phosphatidylinositol glycan anchor biosynthesis, class F gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1557016 Pigf phosphatidylinositol glycan anchor biosynthesis, class F gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1557016 Pigf phosphatidylinositol glycan anchor biosynthesis, class F gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1557016 Pigf phosphatidylinositol glycan anchor biosynthesis, class F gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557017 Bmper BMP-binding endothelial regulator gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19221194 1557017 Bmper BMP-binding endothelial regulator gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:19221194 1557017 Bmper BMP-binding endothelial regulator gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0003842 abnormal metopic suture morphology IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0004342 scapular bone foramen IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0004343 small scapula IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0004444 small supraoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0004506 abnormal pubis morphology IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0004553 absent tracheal cartilage rings IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0004553 absent tracheal cartilage rings IAGP N RGD:5509061 20171214 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0004603 absent vertebral arch IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0004670 small vertebral body IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0004915 abnormal Reichert's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0005226 abnormal vertebral arch development IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0005227 abnormal vertebral body development IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0009575 abnormal pubic symphysis morphology IAGP N RGD:5509061 20181018 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:21737784 1557017 Bmper BMP-binding endothelial regulator gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:19221194 1557017 Bmper BMP-binding endothelial regulator gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:19221194 1557017 Bmper BMP-binding endothelial regulator gene MP:0010827 small lung saccule IAGP N RGD:5509061 20141003 MGI PMID:19221194 1557017 Bmper BMP-binding endothelial regulator gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19221194 1557017 Bmper BMP-binding endothelial regulator gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19221194 1557017 Bmper BMP-binding endothelial regulator gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18789316 1557017 Bmper BMP-binding endothelial regulator gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:19221194 1557017 Bmper BMP-binding endothelial regulator gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0011376 abnormal kidney corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0030120 absent retrotympanic process IAGP N RGD:5509061 20171005 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0030431 wide metopic suture IAGP N RGD:5509061 20171214 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0030844 abnormal pubis body morphology IAGP N RGD:5509061 20181025 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0030867 small thyroid cartilage IAGP N RGD:5509061 20181101 MGI PMID:17035289 1557017 Bmper BMP-binding endothelial regulator gene MP:0030872 small cricoid cartilage IAGP N RGD:5509061 20181101 MGI PMID:17035289 1557018 Mcm7 minichromosome maintenance complex component 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20838603 1557018 Mcm7 minichromosome maintenance complex component 7 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20838603 1557018 Mcm7 minichromosome maintenance complex component 7 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:20838603 1557018 Mcm7 minichromosome maintenance complex component 7 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:20838603 1557018 Mcm7 minichromosome maintenance complex component 7 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20838603 1557018 Mcm7 minichromosome maintenance complex component 7 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20838603 1557018 Mcm7 minichromosome maintenance complex component 7 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20838603 1557019 Timd2 T cell immunoglobulin and mucin domain containing 2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16982865 1557019 Timd2 T cell immunoglobulin and mucin domain containing 2 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16982865 1557019 Timd2 T cell immunoglobulin and mucin domain containing 2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16982865 1557019 Timd2 T cell immunoglobulin and mucin domain containing 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16982865 1557019 Timd2 T cell immunoglobulin and mucin domain containing 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16982865 1557019 Timd2 T cell immunoglobulin and mucin domain containing 2 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:16982865 1557020 Itgbl1 integrin, beta-like 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20240523 MGI 1557020 Itgbl1 integrin, beta-like 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20240523 MGI 1557021 Sestd1 SEC14 and spectrin domains 1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:23696638 1557021 Sestd1 SEC14 and spectrin domains 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:23696638 1557021 Sestd1 SEC14 and spectrin domains 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:23696638 1557021 Sestd1 SEC14 and spectrin domains 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:23696638 1557021 Sestd1 SEC14 and spectrin domains 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23696638 1557021 Sestd1 SEC14 and spectrin domains 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:23696638 1557021 Sestd1 SEC14 and spectrin domains 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:23696638 1557021 Sestd1 SEC14 and spectrin domains 1 gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20141003 MGI PMID:23696638 1557021 Sestd1 SEC14 and spectrin domains 1 gene MP:0003942 abnormal urinary system development IAGP N RGD:5509061 20141003 MGI PMID:23696638 1557021 Sestd1 SEC14 and spectrin domains 1 gene MP:0008999 absent anus IAGP N RGD:5509061 20141003 MGI PMID:23696638 1557021 Sestd1 SEC14 and spectrin domains 1 gene MP:0009252 absent urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:23696638 1557021 Sestd1 SEC14 and spectrin domains 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23696638 1557021 Sestd1 SEC14 and spectrin domains 1 gene MP:0011771 abnormal genital tubercle morphology IAGP N RGD:5509061 20141003 MGI PMID:23696638 1557022 Isyna1 myo-inositol 1-phosphate synthase A1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1557022 Isyna1 myo-inositol 1-phosphate synthase A1 gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20230601 MGI 1557022 Isyna1 myo-inositol 1-phosphate synthase A1 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1557022 Isyna1 myo-inositol 1-phosphate synthase A1 gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20230601 MGI 1557022 Isyna1 myo-inositol 1-phosphate synthase A1 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20230601 MGI 1557022 Isyna1 myo-inositol 1-phosphate synthase A1 gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20230601 MGI 1557022 Isyna1 myo-inositol 1-phosphate synthase A1 gene MP:0001722 pale yolk sac IEA N RGD:5509061 20230601 MGI 1557022 Isyna1 myo-inositol 1-phosphate synthase A1 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20230601 MGI 1557022 Isyna1 myo-inositol 1-phosphate synthase A1 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20230601 MGI 1557022 Isyna1 myo-inositol 1-phosphate synthase A1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20230601 MGI 1557022 Isyna1 myo-inositol 1-phosphate synthase A1 gene MP:0002861 abnormal tail bud morphology IEA N RGD:5509061 20230601 MGI 1557022 Isyna1 myo-inositol 1-phosphate synthase A1 gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20230601 MGI 1557022 Isyna1 myo-inositol 1-phosphate synthase A1 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20230601 MGI 1557022 Isyna1 myo-inositol 1-phosphate synthase A1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557024 Gusb glucuronidase, beta gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20200310 MGI PMID:12700165 1557024 Gusb glucuronidase, beta gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20200310 MGI PMID:2111021 1557024 Gusb glucuronidase, beta gene MP:0000435 shortened head IAGP N RGD:5509061 20200310 MGI PMID:11228259 1557024 Gusb glucuronidase, beta gene MP:0000435 shortened head IAGP N RGD:5509061 20200310 MGI PMID:12700165 1557024 Gusb glucuronidase, beta gene MP:0000435 shortened head IAGP N RGD:5509061 20200310 MGI PMID:9774663 1557024 Gusb glucuronidase, beta gene MP:0000445 short snout IAGP N RGD:5509061 20200310 MGI PMID:2495302 1557024 Gusb glucuronidase, beta gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:11228259 1557024 Gusb glucuronidase, beta gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557024 Gusb glucuronidase, beta gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:12700165 1557024 Gusb glucuronidase, beta gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:2495302 1557024 Gusb glucuronidase, beta gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:9774663 1557024 Gusb glucuronidase, beta gene MP:0000588 thick tail IAGP N RGD:5509061 20200310 MGI PMID:11228259 1557024 Gusb glucuronidase, beta gene MP:0000588 thick tail IAGP N RGD:5509061 20200310 MGI PMID:2495302 1557024 Gusb glucuronidase, beta gene MP:0000588 thick tail IAGP N RGD:5509061 20200310 MGI PMID:9774663 1557024 Gusb glucuronidase, beta gene MP:0000592 short tail IAGP N RGD:5509061 20200310 MGI PMID:2495302 1557024 Gusb glucuronidase, beta gene MP:0000592 short tail IAGP N RGD:5509061 20200310 MGI PMID:9774663 1557024 Gusb glucuronidase, beta gene MP:0001258 decreased body length IEA N RGD:5509061 20111116 MGI 1557024 Gusb glucuronidase, beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:11228259 1557024 Gusb glucuronidase, beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557024 Gusb glucuronidase, beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:12700165 1557024 Gusb glucuronidase, beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:9774663 1557024 Gusb glucuronidase, beta gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557024 Gusb glucuronidase, beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:11228259 1557024 Gusb glucuronidase, beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557024 Gusb glucuronidase, beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:12700165 1557024 Gusb glucuronidase, beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:9774663 1557024 Gusb glucuronidase, beta gene MP:0001783 decreased white adipose tissue amount IEA N RGD:5509061 20111116 MGI 1557024 Gusb glucuronidase, beta gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20200310 MGI PMID:2495302 1557024 Gusb glucuronidase, beta gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:2495302 1557024 Gusb glucuronidase, beta gene MP:0001967 deafness IAGP N RGD:5509061 20200310 MGI PMID:12700165 1557024 Gusb glucuronidase, beta gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557024 Gusb glucuronidase, beta gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:10560917 1557024 Gusb glucuronidase, beta gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:11228259 1557024 Gusb glucuronidase, beta gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:2495302 1557024 Gusb glucuronidase, beta gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:12700165 1557024 Gusb glucuronidase, beta gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557024 Gusb glucuronidase, beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:2111021 1557024 Gusb glucuronidase, beta gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20200310 MGI PMID:2495302 1557024 Gusb glucuronidase, beta gene MP:0002566 abnormal sexual interaction IEA N RGD:5509061 20111116 MGI 1557024 Gusb glucuronidase, beta gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557024 Gusb glucuronidase, beta gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557024 Gusb glucuronidase, beta gene MP:0004470 small nasal bone IAGP N RGD:5509061 20200310 MGI PMID:2495302 1557024 Gusb glucuronidase, beta gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557024 Gusb glucuronidase, beta gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20200310 MGI PMID:10560917 1557024 Gusb glucuronidase, beta gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20200310 MGI PMID:10560917 1557024 Gusb glucuronidase, beta gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20200310 MGI PMID:11228259 1557024 Gusb glucuronidase, beta gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557024 Gusb glucuronidase, beta gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20200310 MGI PMID:2111021 1557024 Gusb glucuronidase, beta gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20200310 MGI PMID:2495302 1557024 Gusb glucuronidase, beta gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20200310 MGI PMID:9774663 1557024 Gusb glucuronidase, beta gene MP:0005060 accumulation of giant lysosomes in kidney/renal tubule cells IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557024 Gusb glucuronidase, beta gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20111116 MGI 1557024 Gusb glucuronidase, beta gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20200310 MGI PMID:2111021 1557024 Gusb glucuronidase, beta gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200310 MGI PMID:2111021 1557024 Gusb glucuronidase, beta gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20200310 MGI PMID:12700165 1557024 Gusb glucuronidase, beta gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:2495302 1557024 Gusb glucuronidase, beta gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557024 Gusb glucuronidase, beta gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557024 Gusb glucuronidase, beta gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557024 Gusb glucuronidase, beta gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12700165 1557024 Gusb glucuronidase, beta gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1557024 Gusb glucuronidase, beta gene MP:0011473 increased urine glycosaminoglycan level IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557024 Gusb glucuronidase, beta gene MP:0011473 increased urine glycosaminoglycan level IAGP N RGD:5509061 20200310 MGI PMID:14583446 1557024 Gusb glucuronidase, beta gene MP:0030066 short face IAGP N RGD:5509061 20200310 MGI PMID:12403825 1557026 Srpx2 sushi-repeat-containing protein, X-linked 2 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20230119 MGI 1557026 Srpx2 sushi-repeat-containing protein, X-linked 2 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20180906 MGI PMID:29920554 1557026 Srpx2 sushi-repeat-containing protein, X-linked 2 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20180906 MGI PMID:29920554 1557026 Srpx2 sushi-repeat-containing protein, X-linked 2 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20180906 MGI PMID:29920554 1557027 Mug1 murinoglobulin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14580373 1557027 Mug1 murinoglobulin 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:10487856 1557027 Mug1 murinoglobulin 1 gene MP:0001657 abnormal induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10487856 1557027 Mug1 murinoglobulin 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:14580373 1557027 Mug1 murinoglobulin 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:10487856 1557027 Mug1 murinoglobulin 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:14580373 1557027 Mug1 murinoglobulin 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:14580373 1557027 Mug1 murinoglobulin 1 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:14580373 1557027 Mug1 murinoglobulin 1 gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:14580373 1557027 Mug1 murinoglobulin 1 gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14580373 1557027 Mug1 murinoglobulin 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14580373 1557027 Mug1 murinoglobulin 1 gene MP:0008054 abnormal uterine NK cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14580373 1557027 Mug1 murinoglobulin 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:10487856 1557027 Mug1 murinoglobulin 1 gene MP:0008806 increased circulating amylase level IAGP N RGD:5509061 20150611 MGI PMID:10487856 1557027 Mug1 murinoglobulin 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10487856 1557027 Mug1 murinoglobulin 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14580373 1557027 Mug1 murinoglobulin 1 gene MP:0011886 increased circulating lipase level IAGP N RGD:5509061 20150611 MGI PMID:10487856 1557027 Mug1 murinoglobulin 1 gene MP:0012726 abnormal uterine spiral artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14580373 1557028 Mrpl12 mitochondrial ribosomal protein L12 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1557028 Mrpl12 mitochondrial ribosomal protein L12 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 1557028 Mrpl12 mitochondrial ribosomal protein L12 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20240620 MGI PMID:37182101 1557028 Mrpl12 mitochondrial ribosomal protein L12 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20240620 MGI PMID:37182101 1557028 Mrpl12 mitochondrial ribosomal protein L12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1557028 Mrpl12 mitochondrial ribosomal protein L12 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20240620 MGI PMID:37182101 1557028 Mrpl12 mitochondrial ribosomal protein L12 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20240620 MGI PMID:37182101 1557028 Mrpl12 mitochondrial ribosomal protein L12 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1557029 Tulp4 TUB like protein 4 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 1557029 Tulp4 TUB like protein 4 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1557029 Tulp4 TUB like protein 4 gene MP:0001260 increased body weight IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0004175 telangiectasia IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0004665 abnormal stapedial artery morphology IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0004880 lung cyst IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0009455 enhanced cued conditioning behavior IEA N RGD:5509061 20240523 MGI 1557029 Tulp4 TUB like protein 4 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1557029 Tulp4 TUB like protein 4 gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1557029 Tulp4 TUB like protein 4 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0011513 abnormal vertebral artery morphology IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0011683 dual inferior vena cava IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0013162 abnormal thyroid gland isthmus morphology IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0013814 abnormal hepatic portal vein connection IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0013834 thin hypoglossal nerve IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0013840 absent segment of posterior cerebral artery IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0013848 subcutaneous edema IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0013876 absent ductus venosus valve IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0013936 abnormal thymus topology IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0013952 retroesophageal left subclavian artery IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0013966 abnormal infrahyoid muscle morphology IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0013970 absent connection between subcutaneous lymph vessels and lymph sac IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0013973 abnormal hepatic vein connection IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0013995 abnormal external carotid artery origin IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557029 Tulp4 TUB like protein 4 gene MP:0020824 abnormal testis tissue architecture IAGP N RGD:5509061 20240215 MGI PMID:38115643 1557030 Magix MAGI family member, X-linked gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230119 MGI 1557030 Magix MAGI family member, X-linked gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 1557030 Magix MAGI family member, X-linked gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20230119 MGI 1557030 Magix MAGI family member, X-linked gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20230119 MGI 1557030 Magix MAGI family member, X-linked gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230119 MGI 1557031 Septin6 septin 6 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220811 MGI 1557031 Septin6 septin 6 gene MP:0000274 enlarged heart IEA N RGD:5509061 20220811 MGI 1557031 Septin6 septin 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16314519 1557031 Septin6 septin 6 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1557032 Tm9sf3 transmembrane 9 superfamily member 3 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1557032 Tm9sf3 transmembrane 9 superfamily member 3 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1557032 Tm9sf3 transmembrane 9 superfamily member 3 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1557032 Tm9sf3 transmembrane 9 superfamily member 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201231 MGI 1557032 Tm9sf3 transmembrane 9 superfamily member 3 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1557032 Tm9sf3 transmembrane 9 superfamily member 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557033 Fundc1 FUN14 domain containing 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1557033 Fundc1 FUN14 domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160915 MGI PMID:24652767 1557033 Fundc1 FUN14 domain containing 1 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20210128 MGI 1557035 Acod1 aconitate decarboxylase 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20161117 MGI PMID:27189937 1557035 Acod1 aconitate decarboxylase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0000202 abnormal circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0000613 abnormal salivary gland morphology IEA N RGD:5509061 20210520 MGI 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17344385 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17344385 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:17380209 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17380209 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:17380209 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17380209 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:17380209 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17380209 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17344385 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17380209 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:17380209 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0001589 abnormal mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20141003 MGI PMID:18495893 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20190228 MGI PMID:25437547 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20200514 MGI 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18177725 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17380209 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:18022372 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:17380209 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:17380209 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0002581 abnormal ileum morphology IEA N RGD:5509061 20210520 MGI 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0002710 increased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:18177725 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18022372 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:18177725 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0002918 abnormal paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:17344385 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:17344385 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:18177725 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:18177725 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20210520 MGI 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:17380209 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18177725 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:18177725 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0004002 abnormal jejunum morphology IEA N RGD:5509061 20210520 MGI 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17380209 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18022372 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18022372 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21040848 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18177725 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18177725 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20190228 MGI PMID:25437547 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:17380209 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:17344385 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0008953 abnormal pancreatic somatostatin secretion IAGP N RGD:5509061 20141003 MGI PMID:18177725 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20141003 MGI PMID:17344385 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20141003 MGI PMID:17344385 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20141003 MGI PMID:17344385 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18177725 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0011267 abnormal excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:18022372 1557036 Cadps2 Ca2+-dependent activator protein for secretion 2 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:17380209 1557038 Rlim ring finger protein, LIM domain interacting gene MP:0000226 abnormal mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1557038 Rlim ring finger protein, LIM domain interacting gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1557038 Rlim ring finger protein, LIM domain interacting gene MP:0000274 enlarged heart IEA N RGD:5509061 20201022 MGI 1557038 Rlim ring finger protein, LIM domain interacting gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20201022 MGI 1557038 Rlim ring finger protein, LIM domain interacting gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20201022 MGI 1557038 Rlim ring finger protein, LIM domain interacting gene MP:0000709 enlarged thymus IEA N RGD:5509061 20201022 MGI 1557038 Rlim ring finger protein, LIM domain interacting gene MP:0001589 abnormal mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1557038 Rlim ring finger protein, LIM domain interacting gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20962847 1557038 Rlim ring finger protein, LIM domain interacting gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:20962847 1557038 Rlim ring finger protein, LIM domain interacting gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20962847 1557038 Rlim ring finger protein, LIM domain interacting gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20201022 MGI 1557038 Rlim ring finger protein, LIM domain interacting gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:20962847 1557038 Rlim ring finger protein, LIM domain interacting gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20201022 MGI 1557038 Rlim ring finger protein, LIM domain interacting gene MP:0010382 abnormal dosage compensation, by inactivation of X chromosome IAGP N RGD:5509061 20141003 MGI PMID:20962847 1557038 Rlim ring finger protein, LIM domain interacting gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20962847 1557039 Parp11 poly (ADP-ribose) polymerase family, member 11 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20161020 MGI PMID:25673562 1557039 Parp11 poly (ADP-ribose) polymerase family, member 11 gene MP:0001925 male infertility IAGP N RGD:5509061 20161020 MGI PMID:25673562 1557039 Parp11 poly (ADP-ribose) polymerase family, member 11 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20161020 MGI PMID:25673562 1557039 Parp11 poly (ADP-ribose) polymerase family, member 11 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1557039 Parp11 poly (ADP-ribose) polymerase family, member 11 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20161020 MGI PMID:25673562 1557039 Parp11 poly (ADP-ribose) polymerase family, member 11 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20161020 MGI PMID:25673562 1557039 Parp11 poly (ADP-ribose) polymerase family, member 11 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20161020 MGI PMID:25673562 1557039 Parp11 poly (ADP-ribose) polymerase family, member 11 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20161020 MGI PMID:25673562 1557039 Parp11 poly (ADP-ribose) polymerase family, member 11 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20161020 MGI PMID:25673562 1557041 Crebzf CREB/ATF bZIP transcription factor gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0001116 small gonad IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0001304 cataract IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0001324 abnormal eye pigmentation IEA N RGD:5509061 20160804 MGI 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20160804 MGI 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20169082 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:20169082 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20169082 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20180201 MGI PMID:12361980 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20180201 MGI PMID:12361980 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0005000 abnormal immune tolerance IAGP N RGD:5509061 20180201 MGI PMID:2464645 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:15308121 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20180201 MGI PMID:15308121 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:20169082 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0009332 abnormal splenocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:15308121 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21947081 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20107607 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0012538 persistent hyaloid artery IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557042 Mcph1 microcephaly, primary autosomal recessive 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:20107607 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15485634 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11520463 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15485634 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:11509691 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11509691 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11520463 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11520463 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11509691 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11520463 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0002221 abnormal lymph organ size IAGP N RGD:5509061 20141003 MGI PMID:11520463 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:11509691 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11520463 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11509691 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0002619 abnormal lymphocyte morphology IEA N RGD:5509061 20190418 MGI 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:18624351 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:15368291 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11509691 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11520463 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11509691 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18624351 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15368291 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:11520463 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008082 increased single-positive T cell number IEA N RGD:5509061 20150507 MGI 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11520463 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18313334 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:11509691 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:11520463 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18624351 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008175 absent follicular B cells IAGP N RGD:5509061 20141003 MGI PMID:18313334 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18313334 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:11509691 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:18313334 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18624351 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11520463 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18313334 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18624351 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008214 increased immature B cell number IEA N RGD:5509061 20111116 MGI 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11520463 1557043 Tnfsf13b tumor necrosis factor (ligand) superfamily, member 13b gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20150507 MGI 1557044 Cpsf6 cleavage and polyadenylation specific factor 6 gene MP:0001924 infertility IAGP N RGD:5509061 20240502 MGI PMID:38416782 1557044 Cpsf6 cleavage and polyadenylation specific factor 6 gene MP:0005159 azoospermia IAGP N RGD:5509061 20240502 MGI PMID:38416782 1557044 Cpsf6 cleavage and polyadenylation specific factor 6 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20240502 MGI PMID:38416782 1557044 Cpsf6 cleavage and polyadenylation specific factor 6 gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20240502 MGI PMID:38416782 1557045 Acnat2 acyl-coenzyme A amino acid N-acyltransferase 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1557045 Acnat2 acyl-coenzyme A amino acid N-acyltransferase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1557048 Tmem241 transmembrane protein 241 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20240620 MGI PMID:37890669 1557048 Tmem241 transmembrane protein 241 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20200402 MGI 1557048 Tmem241 transmembrane protein 241 gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20240620 MGI PMID:37890669 1557048 Tmem241 transmembrane protein 241 gene MP:0014473 increased pulmonary alveolus wall thickness IAGP N RGD:5509061 20240704 MGI PMID:37890669 1557048 Tmem241 transmembrane protein 241 gene MP:0031632 increased lung cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:37890669 1557049 Slitrk4 SLIT and NTRK-like family, member 4 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 1557049 Slitrk4 SLIT and NTRK-like family, member 4 gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20240808 MGI PMID:38736483 1557049 Slitrk4 SLIT and NTRK-like family, member 4 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20240808 MGI PMID:38736483 1557049 Slitrk4 SLIT and NTRK-like family, member 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240808 MGI PMID:38736483 1557049 Slitrk4 SLIT and NTRK-like family, member 4 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20240808 MGI PMID:38736483 1557049 Slitrk4 SLIT and NTRK-like family, member 4 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20240808 MGI PMID:38736483 1557049 Slitrk4 SLIT and NTRK-like family, member 4 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20240808 MGI PMID:38736483 1557049 Slitrk4 SLIT and NTRK-like family, member 4 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20240808 MGI PMID:38736483 1557049 Slitrk4 SLIT and NTRK-like family, member 4 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20240808 MGI PMID:38736483 1557049 Slitrk4 SLIT and NTRK-like family, member 4 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20240808 MGI PMID:38736483 1557049 Slitrk4 SLIT and NTRK-like family, member 4 gene MP:0009455 enhanced cued conditioning behavior IAGP N RGD:5509061 20240808 MGI PMID:38736483 1557049 Slitrk4 SLIT and NTRK-like family, member 4 gene MP:0020852 abnormal olfactory behavior IAGP N RGD:5509061 20240808 MGI PMID:38736483 1557049 Slitrk4 SLIT and NTRK-like family, member 4 gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20240808 MGI PMID:38736483 1557050 Dcp1a decapping mRNA 1A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20210603 MGI PMID:33813271 1557050 Dcp1a decapping mRNA 1A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210603 MGI PMID:33813271 1557050 Dcp1a decapping mRNA 1A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20210603 MGI PMID:33813271 1557050 Dcp1a decapping mRNA 1A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20210603 MGI PMID:33813271 1557051 Lancl3 LanC lantibiotic synthetase component C-like 3 (bacterial) gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220519 MGI 1557051 Lancl3 LanC lantibiotic synthetase component C-like 3 (bacterial) gene MP:0002083 premature death IAGP N RGD:5509061 20240222 MGI PMID:33932340 1557051 Lancl3 LanC lantibiotic synthetase component C-like 3 (bacterial) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180222 MGI PMID:28106097 1557051 Lancl3 LanC lantibiotic synthetase component C-like 3 (bacterial) gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20220519 MGI 1557053 Ahrr aryl-hydrocarbon receptor repressor gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210826 MGI 1557053 Ahrr aryl-hydrocarbon receptor repressor gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1557053 Ahrr aryl-hydrocarbon receptor repressor gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:18022386 1557053 Ahrr aryl-hydrocarbon receptor repressor gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 1557053 Ahrr aryl-hydrocarbon receptor repressor gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210520 MGI 1557053 Ahrr aryl-hydrocarbon receptor repressor gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210520 MGI 1557055 Odad4 outer dynein arm complex subunit 4 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20180201 MGI PMID:27486780 1557055 Odad4 outer dynein arm complex subunit 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:27486780 1557055 Odad4 outer dynein arm complex subunit 4 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20180201 MGI PMID:27486780 1557055 Odad4 outer dynein arm complex subunit 4 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20180201 MGI PMID:27486780 1557055 Odad4 outer dynein arm complex subunit 4 gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20180201 MGI PMID:27486780 1557055 Odad4 outer dynein arm complex subunit 4 gene MP:0010854 lung situs inversus IAGP N RGD:5509061 20180201 MGI PMID:27486780 1557055 Odad4 outer dynein arm complex subunit 4 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:27486780 1557055 Odad4 outer dynein arm complex subunit 4 gene MP:0012093 absent nodal flow IAGP N RGD:5509061 20180201 MGI PMID:27486780 1557058 Myo18b myosin XVIIIb gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1557058 Myo18b myosin XVIIIb gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18761673 1557058 Myo18b myosin XVIIIb gene MP:0004062 dilated heart right atrium IAGP N RGD:5509061 20231221 MGI PMID:18761673 1557058 Myo18b myosin XVIIIb gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1557058 Myo18b myosin XVIIIb gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:18761673 1557058 Myo18b myosin XVIIIb gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:18761673 1557058 Myo18b myosin XVIIIb gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18761673 1557058 Myo18b myosin XVIIIb gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18761673 1557058 Myo18b myosin XVIIIb gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557058 Myo18b myosin XVIIIb gene MP:0031613 fetal cardiomyocyte disarray IAGP N RGD:5509061 20240321 MGI PMID:18761673 1557059 Tspyl2 TSPY-like 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1557059 Tspyl2 TSPY-like 2 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:21738728 1557059 Tspyl2 TSPY-like 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220811 MGI 1557061 Zcchc17 zinc finger, CCHC domain containing 17 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20230119 MGI 1557061 Zcchc17 zinc finger, CCHC domain containing 17 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 1557061 Zcchc17 zinc finger, CCHC domain containing 17 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20180412 MGI PMID:26721440 1557061 Zcchc17 zinc finger, CCHC domain containing 17 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230119 MGI 1557061 Zcchc17 zinc finger, CCHC domain containing 17 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20180412 MGI PMID:26721440 1557061 Zcchc17 zinc finger, CCHC domain containing 17 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20180412 MGI PMID:26721440 1557062 Pcbp1 poly(rC) binding protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170928 MGI PMID:26527618 1557062 Pcbp1 poly(rC) binding protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170928 MGI PMID:26527618 1557062 Pcbp1 poly(rC) binding protein 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20170928 MGI PMID:26527618 1557062 Pcbp1 poly(rC) binding protein 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170928 MGI PMID:26527618 1557063 Mier1 MEIR1 treanscription regulator gene MP:0000745 tremors IEA N RGD:5509061 20160804 MGI 1557063 Mier1 MEIR1 treanscription regulator gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1557063 Mier1 MEIR1 treanscription regulator gene MP:0001512 trunk curl IEA N RGD:5509061 20160804 MGI 1557063 Mier1 MEIR1 treanscription regulator gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20160804 MGI 1557063 Mier1 MEIR1 treanscription regulator gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20160804 MGI 1557063 Mier1 MEIR1 treanscription regulator gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1557063 Mier1 MEIR1 treanscription regulator gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160804 MGI 1557064 Fuom fucose mutarotase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20609214 1557064 Fuom fucose mutarotase gene MP:0001376 abnormal mating receptivity IAGP N RGD:5509061 20141003 MGI PMID:20609214 1557064 Fuom fucose mutarotase gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:20609214 1557064 Fuom fucose mutarotase gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:20609214 1557064 Fuom fucose mutarotase gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:20609214 1557065 Cd84 CD84 antigen gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1557065 Cd84 CD84 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:20153220 1557065 Cd84 CD84 antigen gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25551754 1557065 Cd84 CD84 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20153220 1557065 Cd84 CD84 antigen gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1557065 Cd84 CD84 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20153220 1557065 Cd84 CD84 antigen gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:20153220 1557065 Cd84 CD84 antigen gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:20153220 1557065 Cd84 CD84 antigen gene MP:0009058 decreased interleukin-21 secretion IAGP N RGD:5509061 20141003 MGI PMID:20153220 1557065 Cd84 CD84 antigen gene MP:0010084 abnormal long lived plasma cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20153220 1557068 Ep400 E1A binding protein p400 gene MP:0000215 absent erythrocytes IAGP N RGD:5509061 20141003 MGI PMID:17535249 1557068 Ep400 E1A binding protein p400 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20610385 1557068 Ep400 E1A binding protein p400 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:17535249 1557068 Ep400 E1A binding protein p400 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17535249 1557068 Ep400 E1A binding protein p400 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17535249 1557068 Ep400 E1A binding protein p400 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20610385 1557068 Ep400 E1A binding protein p400 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20610385 1557068 Ep400 E1A binding protein p400 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17535249 1557068 Ep400 E1A binding protein p400 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20610385 1557068 Ep400 E1A binding protein p400 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20610385 1557068 Ep400 E1A binding protein p400 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20610385 1557068 Ep400 E1A binding protein p400 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17535249 1557068 Ep400 E1A binding protein p400 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20610385 1557068 Ep400 E1A binding protein p400 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20610385 1557068 Ep400 E1A binding protein p400 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20610385 1557068 Ep400 E1A binding protein p400 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17535249 1557068 Ep400 E1A binding protein p400 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22615130 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22615130 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20150924 MGI PMID:23168837 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:22615130 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:15128773 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12387740 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0005022 abnormal immature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:22615130 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12387740 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0005461 abnormal dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0005461 abnormal dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15128773 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:22615130 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:22615130 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22615130 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0008122 decreased myeloid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0008122 decreased myeloid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:15128773 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:15128773 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22615130 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22615130 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12387740 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12387740 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10828034 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12387740 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0010740 abnormal dendritic cell chemotaxis IAGP N RGD:5509061 20150924 MGI PMID:23168837 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0013649 decreased CD11b-high dendritic cell number IAGP N RGD:5509061 20150924 MGI PMID:23168837 1557069 Flt3l FMS-like tyrosine kinase 3 ligand gene MP:0013655 decreased CD103-positive CD11b-low dendritic cell number IAGP N RGD:5509061 20150924 MGI PMID:23168837 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:17468755 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:20609353 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:15837621 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:20609353 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:21156286 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:21514245 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0000414 alopecia IAGP N RGD:5509061 20180719 MGI PMID:21088222 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0000423 delayed hair regrowth IAGP N RGD:5509061 20180719 MGI PMID:21156286 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20180719 MGI PMID:21514245 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20180719 MGI PMID:21156286 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20180719 MGI PMID:21514245 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0000692 small spleen IAGP N RGD:5509061 20180719 MGI PMID:15837621 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20180719 MGI PMID:17468755 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20180719 MGI PMID:17468755 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20180719 MGI PMID:21088222 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001200 thick skin IAGP N RGD:5509061 20180719 MGI PMID:21088222 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20180719 MGI PMID:21088222 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20180719 MGI PMID:21088222 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20180719 MGI PMID:21156286 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001234 absent suprabasal layer IAGP N RGD:5509061 20180719 MGI PMID:21088222 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20180719 MGI PMID:21088222 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180719 MGI PMID:10071215 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001263 weight loss IAGP N RGD:5509061 20180719 MGI PMID:21156286 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001265 decreased body size IAGP N RGD:5509061 20180719 MGI PMID:19383288 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20180719 MGI PMID:15837621 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180719 MGI PMID:10071215 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20180719 MGI PMID:21088222 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20180719 MGI PMID:22431510 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20180719 MGI PMID:17468755 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20180719 MGI PMID:20609353 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20180719 MGI PMID:15837621 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20180719 MGI PMID:17468755 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20180719 MGI PMID:15837621 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20180719 MGI PMID:17299132 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20180719 MGI PMID:17468755 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20180719 MGI PMID:20609353 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20180719 MGI PMID:21088222 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:17468755 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:20609353 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:21156286 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:21514245 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:10071215 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:21514245 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:25155958 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20180719 MGI PMID:17468755 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20180719 MGI PMID:18039844 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20180719 MGI PMID:15837621 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20180719 MGI PMID:17468755 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20180719 MGI PMID:20609353 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20180719 MGI PMID:21156286 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20180719 MGI PMID:21088222 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20180719 MGI PMID:21156286 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20180719 MGI PMID:24101512 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20180719 MGI PMID:10071215 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20180719 MGI PMID:24101512 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20180719 MGI PMID:15837621 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20180719 MGI PMID:19383288 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0004882 enlarged lung IAGP N RGD:5509061 20180719 MGI PMID:17468755 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0005014 increased B cell number IAGP N RGD:5509061 20180719 MGI PMID:22431510 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180719 MGI PMID:18039844 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:22431510 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20180719 MGI PMID:21088222 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20180719 MGI PMID:17468755 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20180719 MGI PMID:18039844 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20180719 MGI PMID:20609353 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20180719 MGI PMID:17468755 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20180719 MGI PMID:20609353 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20180719 MGI PMID:22431510 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20180719 MGI PMID:22431510 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20180719 MGI PMID:22431510 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20180719 MGI PMID:22431510 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20180719 MGI PMID:22431510 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20180719 MGI PMID:22431510 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20180719 MGI PMID:22431510 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180719 MGI PMID:22431510 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20180719 MGI PMID:22431510 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20180719 MGI PMID:20609353 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20180719 MGI PMID:22431510 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20180719 MGI PMID:20609353 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0009560 absent epidermis stratum granulosum IAGP N RGD:5509061 20180719 MGI PMID:21088222 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0009759 abnormal hair follicle bulge morphology IAGP N RGD:5509061 20180719 MGI PMID:21088222 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20180719 MGI PMID:17468755 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20180719 MGI PMID:20609353 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0010537 tumor regression IAGP N RGD:5509061 20180719 MGI PMID:21156286 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:10071215 1557071 Polr2a polymerase (RNA) II (DNA directed) polypeptide A gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:10837119 1557072 Sytl3 synaptotagmin-like 3 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 1557073 Pm20d1 peptidase M20 domain containing 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20230119 MGI 1557073 Pm20d1 peptidase M20 domain containing 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20230119 MGI 1557073 Pm20d1 peptidase M20 domain containing 1 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20181018 MGI PMID:29967167 1557073 Pm20d1 peptidase M20 domain containing 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20230119 MGI 1557073 Pm20d1 peptidase M20 domain containing 1 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20181018 MGI PMID:29967167 1557073 Pm20d1 peptidase M20 domain containing 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20181018 MGI PMID:29967167 1557073 Pm20d1 peptidase M20 domain containing 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20181018 MGI PMID:29967167 1557073 Pm20d1 peptidase M20 domain containing 1 gene MP:0011019 abnormal adaptive thermogenesis IAGP N RGD:5509061 20181018 MGI PMID:29967167 1557073 Pm20d1 peptidase M20 domain containing 1 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20181018 MGI PMID:29967167 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20221215 MGI 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0009837 abnormal sperm end piece morphology IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0030591 absent sperm fibrous sheath IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0031351 abnormal sperm flagellum thickness IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557075 Dnah2 dynein, axonemal, heavy chain 2 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220519 MGI PMID:33968937 1557076 Ulk1 unc-51 like kinase 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:18539900 1557076 Ulk1 unc-51 like kinase 1 gene MP:0002424 abnormal reticulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18539900 1557076 Ulk1 unc-51 like kinase 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18539900 1557076 Ulk1 unc-51 like kinase 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:18539900 1557076 Ulk1 unc-51 like kinase 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:18539900 1557076 Ulk1 unc-51 like kinase 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:18539900 1557076 Ulk1 unc-51 like kinase 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:18539900 1557076 Ulk1 unc-51 like kinase 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:18539900 1557076 Ulk1 unc-51 like kinase 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:18539900 1557076 Ulk1 unc-51 like kinase 1 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:18539900 1557076 Ulk1 unc-51 like kinase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21690395 1557080 Ophn1 oligophrenin 1 gene MP:0000402 abnormal zigzag hair morphology IEA N RGD:5509061 20150730 MGI 1557080 Ophn1 oligophrenin 1 gene MP:0000410 waved hair IEA N RGD:5509061 20150730 MGI 1557080 Ophn1 oligophrenin 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0001265 decreased body size IEA N RGD:5509061 20150730 MGI 1557080 Ophn1 oligophrenin 1 gene MP:0001274 curly vibrissae IEA N RGD:5509061 20150730 MGI 1557080 Ophn1 oligophrenin 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0001935 decreased litter size IEA N RGD:5509061 20150730 MGI 1557080 Ophn1 oligophrenin 1 gene MP:0002061 abnormal aggression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0002675 asthenozoospermia IEA N RGD:5509061 20150730 MGI 1557080 Ophn1 oligophrenin 1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:17728457 1557080 Ophn1 oligophrenin 1 gene MP:0010231 transverse fur striping IEA N RGD:5509061 20150730 MGI 1557080 Ophn1 oligophrenin 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20150730 MGI 1557081 Ptcd3 pentatricopeptide repeat domain 3 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1557081 Ptcd3 pentatricopeptide repeat domain 3 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1557081 Ptcd3 pentatricopeptide repeat domain 3 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20210520 MGI 1557081 Ptcd3 pentatricopeptide repeat domain 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557081 Ptcd3 pentatricopeptide repeat domain 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1557082 Tbx10 T-box 10 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:6230750 1557082 Tbx10 T-box 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15118109 1557082 Tbx10 T-box 10 gene MP:0001394 circling IEA N RGD:5509061 20111116 MGI 1557082 Tbx10 T-box 10 gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20162674 1557082 Tbx10 T-box 10 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0002939 head spot IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0002980 abnormal postural reflex IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0004289 abnormal bony labyrinth IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0004317 small vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0004336 small utricle IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0004427 abnormal vestibular labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0004718 abnormal vestibular nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0006409 vestibular ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0009265 delayed eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:15118109 1557082 Tbx10 T-box 10 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:15118109 1557082 Tbx10 T-box 10 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15118109 1557082 Tbx10 T-box 10 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0031447 unilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:5297683 1557082 Tbx10 T-box 10 gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:15118109 1557082 Tbx10 T-box 10 gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:5297683 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20151112 MGI PMID:22689450 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20151112 MGI PMID:22689450 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20180201 MGI PMID:21088218 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0001258 decreased body length IAGP N RGD:5509061 20151112 MGI PMID:22689450 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151112 MGI PMID:22689450 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20180201 MGI PMID:18931664 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20151112 MGI PMID:22689450 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20180201 MGI PMID:17478722 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20180201 MGI PMID:18931664 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20180201 MGI PMID:17478722 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20180201 MGI PMID:18931664 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20180201 MGI PMID:21088218 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20151112 MGI PMID:22689450 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20180201 MGI PMID:21088218 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0001908 abnormal somatosensory cortex physiology IAGP N RGD:5509061 20180201 MGI PMID:21088218 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002083 premature death IAGP N RGD:5509061 20151112 MGI PMID:22689450 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:14687544 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:17478722 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:18931664 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:26931567 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002183 gliosis IAGP N RGD:5509061 20180201 MGI PMID:14687544 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20180201 MGI PMID:10818140 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002801 abnormal long-term object recognition memory IAGP N RGD:5509061 20180201 MGI PMID:17478722 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20180201 MGI PMID:17478722 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20180201 MGI PMID:17478722 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20180201 MGI PMID:17478722 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20180201 MGI PMID:18562603 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20180201 MGI PMID:10818140 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20180201 MGI PMID:14687544 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20180201 MGI PMID:15502844 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20180201 MGI PMID:17478722 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20180201 MGI PMID:18562603 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20180201 MGI PMID:21088218 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20180201 MGI PMID:22492035 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20180201 MGI PMID:25741723 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20180201 MGI PMID:14687544 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20180201 MGI PMID:21088218 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0004254 cerebral amyloid angiopathy IAGP N RGD:5509061 20180201 MGI PMID:21088218 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20180201 MGI PMID:21088218 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20180201 MGI PMID:21088218 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0006203 eye hemorrhage IAGP N RGD:5509061 20151112 MGI PMID:22689450 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20151112 MGI PMID:22689450 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20151112 MGI PMID:22689450 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0008287 abnormal subiculum morphology IAGP N RGD:5509061 20151112 MGI PMID:22689450 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20180201 MGI PMID:21088218 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20180201 MGI PMID:14687544 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20180201 MGI PMID:15502844 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0008569 lethality at weaning IAGP N RGD:5509061 20180201 MGI PMID:26931567 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0009026 abnormal brain pia mater morphology IAGP N RGD:5509061 20180201 MGI PMID:21088218 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20180201 MGI PMID:17478722 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20180201 MGI PMID:17360894 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:26931567 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19273596 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20151112 MGI PMID:22689450 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:26931567 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20151112 MGI PMID:22689450 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240912 MGI PMID:34156424 1557085 Zbtb20 zinc finger and BTB domain containing 20 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20180201 MGI PMID:18562603 1557086 Slc44a4 solute carrier family 44, member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240808 MGI PMID:38713615 1557086 Slc44a4 solute carrier family 44, member 4 gene MP:0001671 abnormal vitamin absorption IAGP N RGD:5509061 20240808 MGI PMID:38713615 1557086 Slc44a4 solute carrier family 44, member 4 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1557086 Slc44a4 solute carrier family 44, member 4 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20240808 MGI PMID:38713615 1557086 Slc44a4 solute carrier family 44, member 4 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1557086 Slc44a4 solute carrier family 44, member 4 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1557086 Slc44a4 solute carrier family 44, member 4 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20240808 MGI PMID:38713615 1557089 Plin3 perilipin 3 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180607 MGI PMID:29440067 1557089 Plin3 perilipin 3 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20180607 MGI PMID:29440067 1557089 Plin3 perilipin 3 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20180607 MGI PMID:29440067 1557089 Plin3 perilipin 3 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20180607 MGI PMID:29440067 1557089 Plin3 perilipin 3 gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20180607 MGI PMID:29440067 1557089 Plin3 perilipin 3 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20180607 MGI PMID:29440067 1557089 Plin3 perilipin 3 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20180607 MGI PMID:29440067 1557089 Plin3 perilipin 3 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180607 MGI PMID:29440067 1557089 Plin3 perilipin 3 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20180607 MGI PMID:29440067 1557089 Plin3 perilipin 3 gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20180607 MGI PMID:29440067 1557089 Plin3 perilipin 3 gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20180607 MGI PMID:29440067 1557089 Plin3 perilipin 3 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20180607 MGI PMID:29440067 1557089 Plin3 perilipin 3 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20180607 MGI PMID:29440067 1557089 Plin3 perilipin 3 gene MP:0020426 abnormal beige fat cell physiology IAGP N RGD:5509061 20180607 MGI PMID:29440067 1557089 Plin3 perilipin 3 gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20180607 MGI PMID:29440067 1557090 Msl3 MSL complex subunit 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1557091 Galnt17 polypeptide N-acetylgalactosaminyltransferase 17 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210805 MGI 1557092 Klrb1b killer cell lectin-like receptor subfamily B member 1B gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20200310 MGI PMID:25612621 1557092 Klrb1b killer cell lectin-like receptor subfamily B member 1B gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20200310 MGI PMID:25612621 1557093 Lgr6 leucine-rich repeat-containing G protein-coupled receptor 6 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1557093 Lgr6 leucine-rich repeat-containing G protein-coupled receptor 6 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1557093 Lgr6 leucine-rich repeat-containing G protein-coupled receptor 6 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1557093 Lgr6 leucine-rich repeat-containing G protein-coupled receptor 6 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1557093 Lgr6 leucine-rich repeat-containing G protein-coupled receptor 6 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1557093 Lgr6 leucine-rich repeat-containing G protein-coupled receptor 6 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1557093 Lgr6 leucine-rich repeat-containing G protein-coupled receptor 6 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1557093 Lgr6 leucine-rich repeat-containing G protein-coupled receptor 6 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230601 MGI 1557093 Lgr6 leucine-rich repeat-containing G protein-coupled receptor 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20223988 1557093 Lgr6 leucine-rich repeat-containing G protein-coupled receptor 6 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20230601 MGI 1557094 Vsig1 V-set and immunoglobulin domain containing 1 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21991385 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:22820399 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22820399 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:22820399 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:21325512 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:22820399 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22820399 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:22820399 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21325512 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:22820399 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:21325512 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:22820399 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:22820399 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:21325512 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22820399 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:22820399 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:21325512 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:22820399 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:22820399 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0011854 cerebral edema IAGP N RGD:5509061 20141003 MGI PMID:22820399 1557097 Srgap3 SLIT-ROBO Rho GTPase activating protein 3 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:21325512 1557098 Tfap2e transcription factor AP-2, epsilon gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:19580868 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20170216 MGI PMID:27162350 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0000158 absent sternum IAGP N RGD:5509061 20141003 MGI PMID:11713269 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11713269 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:11713269 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11713269 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:22343533 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22343533 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20170216 MGI PMID:27162350 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11713269 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20170622 MGI PMID:25043182 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20170622 MGI PMID:25043182 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11713269 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0001967 deafness IAGP N RGD:5509061 20170216 MGI PMID:27162350 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11713269 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:22343533 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:11713269 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20170216 MGI PMID:27162350 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0002989 small kidney IEA N RGD:5509061 20230601 MGI 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20170216 MGI PMID:27162350 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11713269 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:22343533 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:22343533 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:11713269 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20170622 MGI PMID:25043182 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240627 MGI 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0009284 abnormal sympathetic neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:22343533 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20170216 MGI PMID:27162350 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20170216 MGI PMID:27162350 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0009575 abnormal pubic symphysis morphology IAGP N RGD:5509061 20181018 MGI PMID:11713269 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11713269 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20170622 MGI PMID:25043182 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20230601 MGI 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11713269 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11713269 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11713269 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22343533 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20170216 MGI PMID:27162350 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0014409 decreased distortion product otoacoustic emission amplitude IAGP N RGD:5509061 20240405 MGI PMID:27162350 1557099 Ror1 receptor tyrosine kinase-like orphan receptor 1 gene MP:0020359 abnormal ribbon synapse morphology IAGP N RGD:5509061 20170216 MGI PMID:27162350 1557100 Pex26 peroxisomal biogenesis factor 26 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20160811 MGI 1557100 Pex26 peroxisomal biogenesis factor 26 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170105 MGI 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20181227 MGI 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20181227 MGI 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0000706 small thymus IEA N RGD:5509061 20181227 MGI 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20180201 MGI PMID:28948974 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20180201 MGI PMID:28948974 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0001513 limb grasping IAGP N RGD:5509061 20180201 MGI PMID:28948974 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0002989 small kidney IEA N RGD:5509061 20181227 MGI 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20180201 MGI PMID:28948974 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20180201 MGI PMID:28948974 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20180201 MGI PMID:28948974 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20180201 MGI PMID:28948974 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0012286 decreased frequency of paradoxical sleep IAGP N RGD:5509061 20180201 MGI PMID:28948974 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0012292 decreased slow-wave sleep duration IAGP N RGD:5509061 20180201 MGI PMID:28948974 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0020393 increased neuronal precursor proliferation IAGP N RGD:5509061 20180201 MGI PMID:28948974 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0020422 decreased freezing behavior IEA N RGD:5509061 20210128 MGI 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20180201 MGI PMID:28948974 1557102 Upf3b UPF3 regulator of nonsense transcripts homolog B (yeast) gene MP:0021198 abnormal sleep duration IAGP N RGD:5509061 20220922 MGI PMID:28948974 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210520 MGI 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0000599 enlarged liver IEA N RGD:5509061 20210520 MGI 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20201022 MGI 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0002816 colitis IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0012436 increased colon tumor incidence IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557103 Tnfaip8l1 tumor necrosis factor, alpha-induced protein 8-like 1 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20240111 MGI PMID:37459052 1557104 Tuba3b tubulin, alpha 3B gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20211021 MGI PMID:34326397 1557104 Tuba3b tubulin, alpha 3B gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20211021 MGI PMID:34326397 1557104 Tuba3b tubulin, alpha 3B gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20211021 MGI PMID:34326397 1557105 Foxk1 forkhead box K1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:12446708 1557105 Foxk1 forkhead box K1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:10792059 1557105 Foxk1 forkhead box K1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10792059 1557105 Foxk1 forkhead box K1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10792059 1557105 Foxk1 forkhead box K1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10792059 1557105 Foxk1 forkhead box K1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:12446708 1557105 Foxk1 forkhead box K1 gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:10792059 1557105 Foxk1 forkhead box K1 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10792059 1557105 Foxk1 forkhead box K1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10792059 1557105 Foxk1 forkhead box K1 gene MP:0012185 abnormal muscle precursor cell morphology IAGP N RGD:5509061 20190725 MGI PMID:12446708 1557105 Foxk1 forkhead box K1 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:10792059 1557106 Figla folliculogenesis specific basic helix-loop-helix gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:11023867 1557106 Figla folliculogenesis specific basic helix-loop-helix gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11023867 1557106 Figla folliculogenesis specific basic helix-loop-helix gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11023867 1557106 Figla folliculogenesis specific basic helix-loop-helix gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20230518 MGI PMID:32086523 1557106 Figla folliculogenesis specific basic helix-loop-helix gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20230518 MGI PMID:32086523 1557106 Figla folliculogenesis specific basic helix-loop-helix gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:11023867 1557106 Figla folliculogenesis specific basic helix-loop-helix gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20230518 MGI PMID:32086523 1557106 Figla folliculogenesis specific basic helix-loop-helix gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20230518 MGI PMID:32086523 1557106 Figla folliculogenesis specific basic helix-loop-helix gene MP:0011122 absent primordial ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:11023867 1557106 Figla folliculogenesis specific basic helix-loop-helix gene MP:0013507 increased ovary apoptosis IAGP N RGD:5509061 20230518 MGI PMID:32086523 1557106 Figla folliculogenesis specific basic helix-loop-helix gene MP:0031474 increased female germ cell apoptosis IAGP N RGD:5509061 20230615 MGI PMID:32086523 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20200310 MGI 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:9653162 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:18776904 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:18776905 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:18776907 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18776907 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18776905 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18776907 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20200310 MGI PMID:15729333 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20200310 MGI PMID:9653162 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20200310 MGI PMID:18776907 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:18776907 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18776904 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18776905 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18776907 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:21435585 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:23315079 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:23481257 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:9653162 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008077 abnormal CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18776904 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18776905 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18776907 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:23315079 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:9653162 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18258917 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:18776907 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:23481257 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:18776905 1557107 Zbtb7b zinc finger and BTB domain containing 7B gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:18776905 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20160804 MGI 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0000917 obstructive hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:24076219 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001317 abnormal pupil morphology IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0002697 abnormal eye size IEA N RGD:5509061 20160804 MGI 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0003671 abnormal eyelid aperture IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:24076219 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0006241 abnormal placement of pupils IEA N RGD:5509061 20160804 MGI 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:24076219 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0008391 abnormal primordial germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20150122 MGI PMID:22922648 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20170601 MGI PMID:26980188 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:24076219 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20150122 MGI PMID:22922648 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0010102 increased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20141003 MGI PMID:23994477 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24076219 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24076219 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21240276 1557108 Slx4 SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae) gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24076219 1557109 Il36g interleukin 36G gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20201029 MGI PMID:31578266 1557109 Il36g interleukin 36G gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20201029 MGI PMID:28176791 1557109 Il36g interleukin 36G gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20201029 MGI PMID:28176791 1557109 Il36g interleukin 36G gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20201029 MGI PMID:29848754 1557109 Il36g interleukin 36G gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20201029 MGI PMID:28327619 1557109 Il36g interleukin 36G gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20201029 MGI PMID:28327619 1557109 Il36g interleukin 36G gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20201029 MGI PMID:28327619 1557109 Il36g interleukin 36G gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20201029 MGI PMID:28327619 1557109 Il36g interleukin 36G gene MP:0008712 decreased interleukin-9 secretion IAGP N RGD:5509061 20201029 MGI PMID:28327619 1557109 Il36g interleukin 36G gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20201029 MGI PMID:28176791 1557109 Il36g interleukin 36G gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20201029 MGI PMID:31578266 1557109 Il36g interleukin 36G gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20201029 MGI PMID:29848754 1557109 Il36g interleukin 36G gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20201029 MGI PMID:29848754 1557109 Il36g interleukin 36G gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20201029 MGI PMID:28176791 1557109 Il36g interleukin 36G gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20201029 MGI PMID:29848754 1557109 Il36g interleukin 36G gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20201029 MGI PMID:28176791 1557109 Il36g interleukin 36G gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20201029 MGI PMID:29848754 1557109 Il36g interleukin 36G gene MP:0013648 increased CD11b-high dendritic cell number IAGP N RGD:5509061 20201029 MGI PMID:29848754 1557109 Il36g interleukin 36G gene MP:0014229 decreased alveolar macrophage number IAGP N RGD:5509061 20201029 MGI PMID:29848754 1557109 Il36g interleukin 36G gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20201029 MGI PMID:31578266 1557109 Il36g interleukin 36G gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20201029 MGI PMID:29848754 1557109 Il36g interleukin 36G gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20201029 MGI PMID:31578266 1557109 Il36g interleukin 36G gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20201029 MGI PMID:29848754 1557110 Gar1 GAR1 ribonucleoprotein gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20160804 MGI 1557110 Gar1 GAR1 ribonucleoprotein gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20141003 MGI 1557110 Gar1 GAR1 ribonucleoprotein gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20141003 MGI 1557110 Gar1 GAR1 ribonucleoprotein gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20141003 MGI 1557111 Macroh2a2 macroH2A.2 histone gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20240523 MGI 1557111 Macroh2a2 macroH2A.2 histone gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 1557111 Macroh2a2 macroH2A.2 histone gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20240523 MGI 1557111 Macroh2a2 macroH2A.2 histone gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 1557111 Macroh2a2 macroH2A.2 histone gene MP:0001258 decreased body length IAGP N RGD:5509061 20180322 MGI PMID:25312643 1557111 Macroh2a2 macroH2A.2 histone gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180322 MGI PMID:25312643 1557111 Macroh2a2 macroH2A.2 histone gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20240523 MGI 1557111 Macroh2a2 macroH2A.2 histone gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20180322 MGI PMID:25312643 1557111 Macroh2a2 macroH2A.2 histone gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180322 MGI PMID:25312643 1557111 Macroh2a2 macroH2A.2 histone gene MP:0003671 abnormal eyelid aperture IAGP N RGD:5509061 20180322 MGI PMID:25312643 1557111 Macroh2a2 macroH2A.2 histone gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20180322 MGI PMID:25312643 1557111 Macroh2a2 macroH2A.2 histone gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20180322 MGI PMID:25312643 1557111 Macroh2a2 macroH2A.2 histone gene MP:0005251 blepharitis IAGP N RGD:5509061 20180322 MGI PMID:25312643 1557111 Macroh2a2 macroH2A.2 histone gene MP:0005409 darkened coat color IAGP N RGD:5509061 20180322 MGI PMID:25312643 1557111 Macroh2a2 macroH2A.2 histone gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20180322 MGI PMID:25312643 1557111 Macroh2a2 macroH2A.2 histone gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1557111 Macroh2a2 macroH2A.2 histone gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20180322 MGI PMID:25312643 1557111 Macroh2a2 macroH2A.2 histone gene MP:0013745 abnormal eyelid margin morphology IAGP N RGD:5509061 20180322 MGI PMID:25312643 1557113 Icosl icos ligand gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12833154 1557113 Icosl icos ligand gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:14615582 1557113 Icosl icos ligand gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:12833154 1557113 Icosl icos ligand gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:12714510 1557113 Icosl icos ligand gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:14615582 1557113 Icosl icos ligand gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:14615582 1557113 Icosl icos ligand gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12714510 1557113 Icosl icos ligand gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12833154 1557113 Icosl icos ligand gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14615582 1557113 Icosl icos ligand gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:12714510 1557113 Icosl icos ligand gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14615582 1557113 Icosl icos ligand gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:14615582 1557113 Icosl icos ligand gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:12714510 1557113 Icosl icos ligand gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:12833154 1557113 Icosl icos ligand gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:14615582 1557113 Icosl icos ligand gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12833154 1557113 Icosl icos ligand gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:12833154 1557113 Icosl icos ligand gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:12833154 1557113 Icosl icos ligand gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12833154 1557113 Icosl icos ligand gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:14615582 1557113 Icosl icos ligand gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12714510 1557113 Icosl icos ligand gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:14615582 1557113 Icosl icos ligand gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:12714510 1557113 Icosl icos ligand gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12714510 1557113 Icosl icos ligand gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:14615582 1557113 Icosl icos ligand gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:12714510 1557113 Icosl icos ligand gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:12714510 1557113 Icosl icos ligand gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:14615582 1557114 Nrk Nik related kinase gene MP:0004260 enlarged placenta IAGP N RGD:5509061 20141003 MGI PMID:21715335 1557114 Nrk Nik related kinase gene MP:0004514 dystocia IAGP N RGD:5509061 20141003 MGI PMID:21715335 1557114 Nrk Nik related kinase gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:21715335 1557114 Nrk Nik related kinase gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:21715335 1557114 Nrk Nik related kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21715335 1557114 Nrk Nik related kinase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21715335 1557114 Nrk Nik related kinase gene MP:0012098 increased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:21715335 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17098235 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17447844 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17447844 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17447844 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:17098235 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17098235 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17447844 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:17447844 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17447844 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:17447844 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:17098235 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17447844 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:17447844 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17447844 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17098235 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17447844 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17098235 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17447844 1557115 Dmrtc2 doublesex and mab-3 related transcription factor like family C2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:17447844 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20160804 MGI 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180607 MGI PMID:28887018 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20211021 MGI 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20180607 MGI PMID:28887018 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20210520 MGI 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20180607 MGI PMID:28887018 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210520 MGI 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20211021 MGI 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20180607 MGI PMID:28887018 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20180607 MGI PMID:28887018 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24223149 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24223149 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180607 MGI PMID:28887018 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24223149 1557116 Dpp9 dipeptidylpeptidase 9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557118 Kdm5b lysine demethylase 5B gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20150402 MGI PMID:24802759 1557118 Kdm5b lysine demethylase 5B gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20150402 MGI PMID:24802759 1557118 Kdm5b lysine demethylase 5B gene MP:0001258 decreased body length IEA N RGD:5509061 20181227 MGI 1557118 Kdm5b lysine demethylase 5B gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20150402 MGI PMID:24802759 1557118 Kdm5b lysine demethylase 5B gene MP:0001926 female infertility IAGP N RGD:5509061 20150402 MGI PMID:24802759 1557118 Kdm5b lysine demethylase 5B gene MP:0002083 premature death IAGP N RGD:5509061 20150402 MGI PMID:24802759 1557118 Kdm5b lysine demethylase 5B gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20150402 MGI PMID:24802759 1557118 Kdm5b lysine demethylase 5B gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20150402 MGI PMID:24802759 1557118 Kdm5b lysine demethylase 5B gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20181227 MGI 1557118 Kdm5b lysine demethylase 5B gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20150402 MGI PMID:24802759 1557118 Kdm5b lysine demethylase 5B gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20150402 MGI PMID:24802759 1557118 Kdm5b lysine demethylase 5B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557119 Tmprss11e transmembrane protease, serine 11e gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20191031 MGI PMID:31501243 1557120 Atp9b ATPase, class II, type 9B gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1557120 Atp9b ATPase, class II, type 9B gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1557122 Il22ra1 interleukin 22 receptor, alpha 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:24211183 1557122 Il22ra1 interleukin 22 receptor, alpha 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:24211183 1557122 Il22ra1 interleukin 22 receptor, alpha 1 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20210617 MGI PMID:33753942 1557122 Il22ra1 interleukin 22 receptor, alpha 1 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1557122 Il22ra1 interleukin 22 receptor, alpha 1 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 1557122 Il22ra1 interleukin 22 receptor, alpha 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:24211183 1557122 Il22ra1 interleukin 22 receptor, alpha 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160804 MGI 1557122 Il22ra1 interleukin 22 receptor, alpha 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20210617 MGI PMID:33753942 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210826 MGI 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20240523 MGI 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230601 MGI 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20230601 MGI 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19047684 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19047684 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:21435586 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:21435586 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19047684 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:21435586 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:19047684 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19047684 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:19047684 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0011951 increased cardiac stroke volume IEA N RGD:5509061 20231207 MGI 1557123 Rsad2 radical S-adenosyl methionine domain containing 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1557126 Hoxb7 homeobox B7 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9784603 1557126 Hoxb7 homeobox B7 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:9784603 1557126 Hoxb7 homeobox B7 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:9784603 1557126 Hoxb7 homeobox B7 gene MP:0012283 decreased sternebra number IAGP N RGD:5509061 20141003 MGI PMID:9784603 1557127 Tmem70 transmembrane protein 70 gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20210520 MGI 1557127 Tmem70 transmembrane protein 70 gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20190502 MGI 1557127 Tmem70 transmembrane protein 70 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1557127 Tmem70 transmembrane protein 70 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170803 MGI PMID:28173120 1557127 Tmem70 transmembrane protein 70 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20190502 MGI 1557127 Tmem70 transmembrane protein 70 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20190502 MGI 1557127 Tmem70 transmembrane protein 70 gene MP:0002188 small heart IAGP N RGD:5509061 20170803 MGI PMID:28173120 1557127 Tmem70 transmembrane protein 70 gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20190502 MGI 1557127 Tmem70 transmembrane protein 70 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20170803 MGI PMID:28173120 1557127 Tmem70 transmembrane protein 70 gene MP:0003794 delayed somite formation IAGP N RGD:5509061 20170803 MGI PMID:28173120 1557127 Tmem70 transmembrane protein 70 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20170803 MGI PMID:28173120 1557127 Tmem70 transmembrane protein 70 gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20170803 MGI PMID:28173120 1557127 Tmem70 transmembrane protein 70 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20170803 MGI PMID:28173120 1557127 Tmem70 transmembrane protein 70 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20170803 MGI PMID:28173120 1557127 Tmem70 transmembrane protein 70 gene MP:0010052 increased grip strength IEA N RGD:5509061 20231207 MGI 1557127 Tmem70 transmembrane protein 70 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20170803 MGI PMID:28173120 1557127 Tmem70 transmembrane protein 70 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170803 MGI PMID:28173120 1557127 Tmem70 transmembrane protein 70 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557127 Tmem70 transmembrane protein 70 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20170803 MGI PMID:28173120 1557127 Tmem70 transmembrane protein 70 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20170803 MGI PMID:28173120 1557127 Tmem70 transmembrane protein 70 gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20170803 MGI PMID:28173120 1557127 Tmem70 transmembrane protein 70 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20170803 MGI PMID:28173120 1557127 Tmem70 transmembrane protein 70 gene MP:0012708 delayed rostral neuropore closure IAGP N RGD:5509061 20170803 MGI PMID:28173120 1557127 Tmem70 transmembrane protein 70 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1557127 Tmem70 transmembrane protein 70 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:28173120 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20201112 MGI PMID:31634484 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20171012 MGI PMID:23267082 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201112 MGI PMID:31634484 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0001695 abnormal gastrulation IEA N RGD:5509061 20111116 MGI 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:23267082 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0002188 small heart IAGP N RGD:5509061 20201112 MGI PMID:31634484 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20201112 MGI PMID:31634484 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:23267082 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20201112 MGI PMID:31634484 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0003821 decreased left ventricle diastolic pressure IAGP N RGD:5509061 20201112 MGI PMID:31634484 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20201112 MGI PMID:31634484 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20201112 MGI PMID:31634484 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:23267082 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20201112 MGI PMID:31634484 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20201112 MGI PMID:31634484 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:23267082 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20201112 MGI PMID:31634484 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20201112 MGI PMID:31634484 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:22966205 1557128 Nono non-POU-domain-containing, octamer binding protein gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:23267082 1557129 Zfp69 zinc finger protein 69 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20201022 MGI 1557129 Zfp69 zinc finger protein 69 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20211021 MGI 1557130 Stard3 StAR related lipid transfer domain containing 3 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14963026 1557131 Fam184b family with sequence similarity 184, member B gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20221215 MGI 1557131 Fam184b family with sequence similarity 184, member B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16807365 1557131 Fam184b family with sequence similarity 184, member B gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20210805 MGI 1557132 Gpr75 G protein-coupled receptor 75 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20240905 MGI PMID:36978267 1557132 Gpr75 G protein-coupled receptor 75 gene MP:0003213 decreased susceptibility to age related obesity IAGP N RGD:5509061 20240905 MGI PMID:36978267 1557132 Gpr75 G protein-coupled receptor 75 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20231116 MGI PMID:37840219 1557132 Gpr75 G protein-coupled receptor 75 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20231116 MGI PMID:37840219 1557132 Gpr75 G protein-coupled receptor 75 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20231116 MGI PMID:37840219 1557132 Gpr75 G protein-coupled receptor 75 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20231116 MGI PMID:37840219 1557132 Gpr75 G protein-coupled receptor 75 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20240905 MGI PMID:36978267 1557132 Gpr75 G protein-coupled receptor 75 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20231116 MGI PMID:37840219 1557132 Gpr75 G protein-coupled receptor 75 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20231116 MGI PMID:37840219 1557133 Setd6 SET domain containing 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1557133 Setd6 SET domain containing 6 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1557133 Setd6 SET domain containing 6 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220519 MGI 1557133 Setd6 SET domain containing 6 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20231207 MGI 1557133 Setd6 SET domain containing 6 gene MP:0002833 increased heart weight IEA N RGD:5509061 20231207 MGI 1557133 Setd6 SET domain containing 6 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220519 MGI 1557133 Setd6 SET domain containing 6 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220519 MGI 1557133 Setd6 SET domain containing 6 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220519 MGI 1557133 Setd6 SET domain containing 6 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220519 MGI 1557133 Setd6 SET domain containing 6 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1557133 Setd6 SET domain containing 6 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20220519 MGI 1557133 Setd6 SET domain containing 6 gene MP:0012121 sclerocornea IEA N RGD:5509061 20160421 MGI 1557136 Mterf4 mitochondrial transcription termination factor 4 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:21531335 1557136 Mterf4 mitochondrial transcription termination factor 4 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21531335 1557136 Mterf4 mitochondrial transcription termination factor 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21531335 1557136 Mterf4 mitochondrial transcription termination factor 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21531335 1557136 Mterf4 mitochondrial transcription termination factor 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21531335 1557136 Mterf4 mitochondrial transcription termination factor 4 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:21531335 1557136 Mterf4 mitochondrial transcription termination factor 4 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:21531335 1557136 Mterf4 mitochondrial transcription termination factor 4 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:21531335 1557136 Mterf4 mitochondrial transcription termination factor 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21531335 1557136 Mterf4 mitochondrial transcription termination factor 4 gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:21531335 1557136 Mterf4 mitochondrial transcription termination factor 4 gene MP:0011389 absent optic disk IAGP N RGD:5509061 20141003 MGI PMID:21531335 1557137 Clec1a C-type lectin domain family 1, member a gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20221124 MGI PMID:35135958 1557137 Clec1a C-type lectin domain family 1, member a gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20221124 MGI PMID:35135958 1557137 Clec1a C-type lectin domain family 1, member a gene MP:0011823 decreased CD8-positive, alpha-beta memory T cell proliferation IAGP N RGD:5509061 20221124 MGI PMID:35135958 1557138 Ctnnbl1 catenin, beta like 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20161013 MGI PMID:23343763 1557138 Ctnnbl1 catenin, beta like 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20161013 MGI PMID:23343763 1557138 Ctnnbl1 catenin, beta like 1 gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20161013 MGI PMID:23343763 1557138 Ctnnbl1 catenin, beta like 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20161013 MGI PMID:23343763 1557138 Ctnnbl1 catenin, beta like 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20161013 MGI PMID:23343763 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22706340 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:22706340 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:9384589 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10229183 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:9384589 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:10229183 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:9384589 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:22706340 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9384589 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10229183 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0005022 abnormal immature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10229183 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10229183 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9384589 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9384589 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:10229183 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9384589 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9384589 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:9384589 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10229183 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9384589 1557143 Spib Spi-B transcription factor (Spi-1/PU.1 related) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10229183 1557144 Elavl4 ELAV like RNA binding protein 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1557144 Elavl4 ELAV like RNA binding protein 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15764704 1557144 Elavl4 ELAV like RNA binding protein 4 gene MP:0001406 abnormal gait IEA N RGD:5509061 20200514 MGI 1557144 Elavl4 ELAV like RNA binding protein 4 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15764704 1557144 Elavl4 ELAV like RNA binding protein 4 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:15764704 1557144 Elavl4 ELAV like RNA binding protein 4 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15764704 1557144 Elavl4 ELAV like RNA binding protein 4 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:15764704 1557144 Elavl4 ELAV like RNA binding protein 4 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15764704 1557144 Elavl4 ELAV like RNA binding protein 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 1557144 Elavl4 ELAV like RNA binding protein 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22998874 1557144 Elavl4 ELAV like RNA binding protein 4 gene MP:0030737 decreased glutamic acid level IAGP N RGD:5509061 20180927 MGI PMID:22998874 1557146 Hoxc13 homeobox C13 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:9420327 1557146 Hoxc13 homeobox C13 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:9789037 1557146 Hoxc13 homeobox C13 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:9789037 1557146 Hoxc13 homeobox C13 gene MP:0000425 loss of eyelid cilia IAGP N RGD:5509061 20141003 MGI PMID:9420327 1557146 Hoxc13 homeobox C13 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20220217 MGI PMID:7000960 1557146 Hoxc13 homeobox C13 gene MP:0000580 deformed nails IAGP N RGD:5509061 20141003 MGI PMID:9420327 1557146 Hoxc13 homeobox C13 gene MP:0000580 deformed nails IAGP N RGD:5509061 20141003 MGI PMID:9789037 1557146 Hoxc13 homeobox C13 gene MP:0000582 toenail hyperkeratosis IEA N RGD:5509061 20220217 MGI 1557146 Hoxc13 homeobox C13 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:9420327 1557146 Hoxc13 homeobox C13 gene MP:0000749 muscle degeneration IEA N RGD:5509061 20220217 MGI 1557146 Hoxc13 homeobox C13 gene MP:0000763 abnormal filiform papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:9420327 1557146 Hoxc13 homeobox C13 gene MP:0000763 abnormal filiform papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:9789037 1557146 Hoxc13 homeobox C13 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9420327 1557146 Hoxc13 homeobox C13 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20220217 MGI PMID:7000960 1557146 Hoxc13 homeobox C13 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:9420327 1557146 Hoxc13 homeobox C13 gene MP:0001265 decreased body size IEA N RGD:5509061 20220217 MGI 1557146 Hoxc13 homeobox C13 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:9420327 1557146 Hoxc13 homeobox C13 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20220217 MGI 1557146 Hoxc13 homeobox C13 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:9420327 1557146 Hoxc13 homeobox C13 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:9789037 1557146 Hoxc13 homeobox C13 gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20220217 MGI PMID:21020475 1557146 Hoxc13 homeobox C13 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20220217 MGI PMID:7000960 1557146 Hoxc13 homeobox C13 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9420327 1557146 Hoxc13 homeobox C13 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20220217 MGI PMID:7000960 1557146 Hoxc13 homeobox C13 gene MP:0003810 abnormal hair cuticle IEA N RGD:5509061 20220217 MGI 1557146 Hoxc13 homeobox C13 gene MP:0003815 hairless IAGP N RGD:5509061 20220217 MGI PMID:7000960 1557146 Hoxc13 homeobox C13 gene MP:0003848 brittle hair IAGP N RGD:5509061 20141003 MGI PMID:9420327 1557146 Hoxc13 homeobox C13 gene MP:0003848 brittle hair IAGP N RGD:5509061 20220217 MGI PMID:21020475 1557146 Hoxc13 homeobox C13 gene MP:0004614 caudal vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9420327 1557146 Hoxc13 homeobox C13 gene MP:0008770 decreased survivor rate IEA N RGD:5509061 20220217 MGI 1557146 Hoxc13 homeobox C13 gene MP:0010233 hairless tail IAGP N RGD:5509061 20141003 MGI PMID:9420327 1557146 Hoxc13 homeobox C13 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9420327 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11159343 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11689686 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160204 MGI PMID:23633960 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557147 H1f3 H1.3 linker histone, cluster member gene MP:0012156 rostral-caudal axis duplication IAGP N RGD:5509061 20141003 MGI PMID:12808097 1557148 Vnn3 vanin 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1557148 Vnn3 vanin 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1557148 Vnn3 vanin 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1557148 Vnn3 vanin 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1557148 Vnn3 vanin 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1557148 Vnn3 vanin 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1557148 Vnn3 vanin 3 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230601 MGI 1557148 Vnn3 vanin 3 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 1557148 Vnn3 vanin 3 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20230601 MGI 1557148 Vnn3 vanin 3 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1557148 Vnn3 vanin 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1557148 Vnn3 vanin 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1557148 Vnn3 vanin 3 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20240523 MGI 1557148 Vnn3 vanin 3 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20230601 MGI 1557148 Vnn3 vanin 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20240523 MGI 1557150 Golga4 golgin A4 gene MP:0002626 increased heart rate IEA N RGD:5509061 20231207 MGI 1557150 Golga4 golgin A4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1557151 Map2k7 mitogen-activated protein kinase kinase 7 gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21317887 1557151 Map2k7 mitogen-activated protein kinase kinase 7 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:21317887 1557151 Map2k7 mitogen-activated protein kinase kinase 7 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21317887 1557151 Map2k7 mitogen-activated protein kinase kinase 7 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21317887 1557151 Map2k7 mitogen-activated protein kinase kinase 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21317887 1557151 Map2k7 mitogen-activated protein kinase kinase 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21317887 1557151 Map2k7 mitogen-activated protein kinase kinase 7 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22114267 1557151 Map2k7 mitogen-activated protein kinase kinase 7 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:22114267 1557151 Map2k7 mitogen-activated protein kinase kinase 7 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21317887 1557151 Map2k7 mitogen-activated protein kinase kinase 7 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:21317887 1557151 Map2k7 mitogen-activated protein kinase kinase 7 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:22114267 1557151 Map2k7 mitogen-activated protein kinase kinase 7 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:22899651 1557151 Map2k7 mitogen-activated protein kinase kinase 7 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21317887 1557151 Map2k7 mitogen-activated protein kinase kinase 7 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10811224 1557151 Map2k7 mitogen-activated protein kinase kinase 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557152 Edn3 endothelin 3 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:8001160 1557152 Edn3 endothelin 3 gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:5917257 1557152 Edn3 endothelin 3 gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:8001160 1557152 Edn3 endothelin 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8001160 1557152 Edn3 endothelin 3 gene MP:0002557 abnormal social/conspecific interaction behavior IEA N RGD:5509061 20111116 MGI 1557152 Edn3 endothelin 3 gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:14138974 1557152 Edn3 endothelin 3 gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:5917257 1557152 Edn3 endothelin 3 gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20141003 MGI PMID:8001160 1557152 Edn3 endothelin 3 gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:14138974 1557152 Edn3 endothelin 3 gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:17516928 1557152 Edn3 endothelin 3 gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:5917257 1557152 Edn3 endothelin 3 gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:8001160 1557152 Edn3 endothelin 3 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:14138974 1557152 Edn3 endothelin 3 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:14138974 1557152 Edn3 endothelin 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14138974 1557152 Edn3 endothelin 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:5917257 1557152 Edn3 endothelin 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17516928 1557152 Edn3 endothelin 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8001160 1557153 Serac1 serine active site containing 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20190502 MGI 1557153 Serac1 serine active site containing 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20190502 MGI 1557153 Serac1 serine active site containing 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20181227 MGI 1557153 Serac1 serine active site containing 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1557153 Serac1 serine active site containing 1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20181227 MGI 1557153 Serac1 serine active site containing 1 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0006037 abnormal mitochondrial fission IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0009453 enhanced contextual conditioning behavior IEA N RGD:5509061 20211021 MGI 1557153 Serac1 serine active site containing 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0010028 aciduria IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0013806 encephalopathy IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0014388 decreased hepatocyte mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0014389 decreased skeletal muscle fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20201231 MGI 1557153 Serac1 serine active site containing 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1557153 Serac1 serine active site containing 1 gene MP:0021002 brain lesion IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557153 Serac1 serine active site containing 1 gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20220811 MGI PMID:35235340 1557156 Tssk4 testis-specific serine kinase 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20180809 MGI PMID:25361759 1557156 Tssk4 testis-specific serine kinase 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20180809 MGI PMID:25361759 1557156 Tssk4 testis-specific serine kinase 4 gene MP:0004222 iris synechia IEA N RGD:5509061 20190502 MGI 1557156 Tssk4 testis-specific serine kinase 4 gene MP:0009280 decreased activated sperm motility IAGP N RGD:5509061 20180809 MGI PMID:25361759 1557156 Tssk4 testis-specific serine kinase 4 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20180809 MGI PMID:25361759 1557156 Tssk4 testis-specific serine kinase 4 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20180809 MGI PMID:25361759 1557156 Tssk4 testis-specific serine kinase 4 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20180809 MGI PMID:25361759 1557157 Zfp704 zinc finger protein 704 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17693064 1557157 Zfp704 zinc finger protein 704 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0009591 increased liver adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0010288 increased gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0010367 increased spindle cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20240523 MGI 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0014128 increased Harderian gland adenocarcinoma incidence IAGP N RGD:5509061 20160317 MGI PMID:21901109 1557158 Atad5 ATPase family, AAA domain containing 5 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:21901109 1557159 C1ra complement component 1, r subcomponent A gene MP:0002282 abnormal trachea morphology IEA N RGD:5509061 20170105 MGI 1557159 C1ra complement component 1, r subcomponent A gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20230601 MGI 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19767295 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20190207 MGI PMID:30592498 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:19767295 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19767295 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20190207 MGI PMID:30592498 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:19767295 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20190207 MGI PMID:30592498 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:19767295 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:19767295 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0014333 short retina cone cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:19767295 1557161 Cngb3 cyclic nucleotide gated channel beta 3 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:19767295 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:23290137 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21641550 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:23290137 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:23290137 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23290137 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23290137 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23290137 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21986498 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:21986498 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23290137 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:23290137 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21641550 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:21641550 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23290137 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:23290137 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23290137 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:21641550 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:23290137 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23290137 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21641550 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21986498 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:21986498 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1557162 Ptpmt1 protein tyrosine phosphatase, mitochondrial 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:21986498 1557163 Mafa MAF bZIP transcription factor A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15923615 1557163 Mafa MAF bZIP transcription factor A gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:15923615 1557163 Mafa MAF bZIP transcription factor A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20213756 1557163 Mafa MAF bZIP transcription factor A gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15923615 1557163 Mafa MAF bZIP transcription factor A gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15923615 1557163 Mafa MAF bZIP transcription factor A gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:15923615 1557163 Mafa MAF bZIP transcription factor A gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15923615 1557163 Mafa MAF bZIP transcription factor A gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15923615 1557168 Bsx brain specific homeobox gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17485440 1557168 Bsx brain specific homeobox gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17485440 1557168 Bsx brain specific homeobox gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17550780 1557168 Bsx brain specific homeobox gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:17550780 1557168 Bsx brain specific homeobox gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17550780 1557168 Bsx brain specific homeobox gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17550780 1557168 Bsx brain specific homeobox gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17550780 1557168 Bsx brain specific homeobox gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17550780 1557168 Bsx brain specific homeobox gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:17485440 1557168 Bsx brain specific homeobox gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17550780 1557168 Bsx brain specific homeobox gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:17550780 1557168 Bsx brain specific homeobox gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17550780 1557168 Bsx brain specific homeobox gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:17485440 1557168 Bsx brain specific homeobox gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:17485440 1557168 Bsx brain specific homeobox gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:17485440 1557168 Bsx brain specific homeobox gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:17550780 1557168 Bsx brain specific homeobox gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:17550780 1557168 Bsx brain specific homeobox gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17550780 1557168 Bsx brain specific homeobox gene MP:0014126 increased mammary gland apoptosis IAGP N RGD:5509061 20160317 MGI PMID:17485440 1557169 Lypd1 Ly6/Plaur domain containing 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19246390 1557169 Lypd1 Ly6/Plaur domain containing 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19246390 1557169 Lypd1 Ly6/Plaur domain containing 1 gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:19246390 1557169 Lypd1 Ly6/Plaur domain containing 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19246390 1557169 Lypd1 Ly6/Plaur domain containing 1 gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:19246390 1557171 Zfp553 zinc finger protein 553 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IEA N RGD:5509061 20141003 MGI 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20200116 MGI PMID:29379415 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20200507 MGI PMID:31174210 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11983912 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:15326152 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200116 MGI PMID:29379415 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200507 MGI PMID:31174210 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:15326152 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:16088326 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20200507 MGI PMID:31174210 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20200507 MGI PMID:31174210 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:16088326 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20200507 MGI PMID:31174210 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11983912 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16088326 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20200116 MGI PMID:17652759 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16088326 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16088326 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16088326 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16088326 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20200116 MGI PMID:29379415 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16088326 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11983912 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20200507 MGI PMID:31174210 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0005201 abnormal retina pigment epithelium morphology IEA N RGD:5509061 20111116 MGI 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0005240 abnormal amacrine cell morphology IEA N RGD:5509061 20111116 MGI 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20200507 MGI PMID:31174210 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11983912 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15326152 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16088326 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20200116 MGI PMID:29379415 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20200507 MGI PMID:31174210 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15326152 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16088326 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18245825 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20200116 MGI PMID:29379415 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:11983912 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:11983912 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:17652759 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:29379415 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:29379415 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200507 MGI PMID:31174210 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:11983912 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:17652759 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:29379415 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200116 MGI PMID:17652759 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008520 disorganized retina outer plexiform layer IAGP N RGD:5509061 20200116 MGI PMID:17652759 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008520 disorganized retina outer plexiform layer IAGP N RGD:5509061 20200116 MGI PMID:29379415 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20200116 MGI PMID:29379415 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008581 disorganized photoreceptor inner segment IAGP N RGD:5509061 20200116 MGI PMID:17652759 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20200116 MGI PMID:29379415 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:11983912 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20200116 MGI PMID:17652759 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200116 MGI PMID:17652759 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200116 MGI PMID:17652759 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200507 MGI PMID:31174210 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:17652759 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200507 MGI PMID:31174210 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:17652759 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:29379415 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200507 MGI PMID:31174210 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0014333 short retina cone cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:31174210 1557176 Rs1 retinoschisis (X-linked, juvenile) 1 (human) gene MP:0020816 decreased photoreceptor outer segment number IAGP N RGD:5509061 20200116 MGI PMID:29379415 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0000111 cleft palate IEA N RGD:5509061 20111116 MGI 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20150827 MGI PMID:23936366 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23936366 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:23936366 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:23936366 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20181227 MGI 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:23936366 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:23936366 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:23936366 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0005534 decreased body temperature IEA N RGD:5509061 20211021 MGI 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:23936366 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:23936366 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23936366 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23936366 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20141003 MGI PMID:23936366 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0013140 excessive vocalization IAGP N RGD:5509061 20141003 MGI PMID:23936366 1557177 Ckap5 cytoskeleton associated protein 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1557180 Lvrn laeverin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:30745494 1557184 Lyzl1 lysozyme-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1557184 Lyzl1 lysozyme-like 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20170406 MGI 1557189 Tspan6 tetraspanin 6 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20210401 MGI PMID:28207852 1557189 Tspan6 tetraspanin 6 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20210401 MGI PMID:28207852 1557189 Tspan6 tetraspanin 6 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20210401 MGI PMID:28207852 1557189 Tspan6 tetraspanin 6 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20210401 MGI PMID:28207852 1557190 Siglecl2 Siglec family like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1557191 Lamtor2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17178906 1557191 Lamtor2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:17178906 1557191 Lamtor2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:17178906 1557191 Lamtor2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17178906 1557191 Lamtor2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:17178906 1557191 Lamtor2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:17178906 1557191 Lamtor2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:17178906 1557191 Lamtor2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17178906 1557191 Lamtor2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:17178906 1557191 Lamtor2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17178906 1557191 Lamtor2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17178906 1557191 Lamtor2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17178906 1557192 Pcdh10 protocadherin 10 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:17721516 1557192 Pcdh10 protocadherin 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17721516 1557192 Pcdh10 protocadherin 10 gene MP:0001399 hyperactivity IEA N RGD:5509061 20221103 MGI 1557192 Pcdh10 protocadherin 10 gene MP:0001406 abnormal gait IEA N RGD:5509061 20221103 MGI 1557192 Pcdh10 protocadherin 10 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17721516 1557192 Pcdh10 protocadherin 10 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20221103 MGI 1557192 Pcdh10 protocadherin 10 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17721516 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16777961 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19164512 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16777961 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:19164512 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16777961 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19164512 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16777961 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16777961 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11118202 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16777961 1557193 Xrcc2 X-ray repair complementing defective repair in Chinese hamster cells 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:11118202 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11818962 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:11818962 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:11818962 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0000433 microcephaly IAGP N RGD:5509061 20200416 MGI PMID:31730647 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:11818962 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0000562 polydactyly IAGP N RGD:5509061 20200402 MGI PMID:31730647 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20200402 MGI PMID:31730647 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0000914 exencephaly IAGP N RGD:5509061 20200402 MGI PMID:31730647 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0001260 increased body weight IEA N RGD:5509061 20181011 MGI 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11818962 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141030 MGI PMID:24700869 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11818962 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:11818962 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:11818962 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20200416 MGI PMID:31730647 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141030 MGI PMID:24700869 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0004677 truncated ribs IAGP N RGD:5509061 20141003 MGI PMID:11818962 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0004755 abnormal loop of Henle morphology IAGP N RGD:5509061 20141030 MGI PMID:24700869 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20200402 MGI PMID:31730647 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141030 MGI PMID:24700869 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141030 MGI PMID:24700869 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141030 MGI PMID:24700869 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200402 MGI PMID:31730647 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141030 MGI PMID:24700869 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0012547 spina bifida cystica IAGP N RGD:5509061 20200402 MGI PMID:31730647 1557198 Ttc21b tetratricopeptide repeat domain 21B gene MP:0020383 decreased kidney epithelial cell primary cilium length IAGP N RGD:5509061 20161013 MGI PMID:24700869 1557199 Nyx nyctalopin gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:12506099 1557199 Nyx nyctalopin gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16597347 1557199 Nyx nyctalopin gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22896717 1557199 Nyx nyctalopin gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:9804152 1557199 Nyx nyctalopin gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16597347 1557199 Nyx nyctalopin gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:9804152 1557199 Nyx nyctalopin gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:9804152 1557199 Nyx nyctalopin gene MP:0010749 absent visual evoked potential IAGP N RGD:5509061 20141003 MGI PMID:9804152 1557203 Snrnp200 small nuclear ribonucleoprotein 200 (U5) gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 1557203 Snrnp200 small nuclear ribonucleoprotein 200 (U5) gene MP:0000274 enlarged heart IEA N RGD:5509061 20160811 MGI 1557203 Snrnp200 small nuclear ribonucleoprotein 200 (U5) gene MP:0002750 exophthalmos IEA N RGD:5509061 20230601 MGI 1557203 Snrnp200 small nuclear ribonucleoprotein 200 (U5) gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20230601 MGI 1557203 Snrnp200 small nuclear ribonucleoprotein 200 (U5) gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20111116 MGI 1557203 Snrnp200 small nuclear ribonucleoprotein 200 (U5) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557203 Snrnp200 small nuclear ribonucleoprotein 200 (U5) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1557205 Atg9a autophagy related 9A gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20200310 MGI PMID:19926846 1557205 Atg9a autophagy related 9A gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20200310 MGI PMID:19926846 1557205 Atg9a autophagy related 9A gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20200310 MGI PMID:19926846 1557205 Atg9a autophagy related 9A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19926846 1557205 Atg9a autophagy related 9A gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20200310 MGI PMID:19926846 1557205 Atg9a autophagy related 9A gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200310 MGI PMID:19926846 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210520 MGI 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20231123 MGI PMID:35840571 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20231123 MGI PMID:35840571 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20220811 MGI PMID:35789858 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20231123 MGI PMID:35840571 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20200402 MGI 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20220811 MGI PMID:35789858 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20220811 MGI PMID:35789858 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20220811 MGI PMID:35789858 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20220811 MGI PMID:35789858 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0003063 increased coping response IAGP N RGD:5509061 20220811 MGI PMID:35789858 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20220811 MGI PMID:35789858 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0003877 abnormal serotonergic neuron morphology IAGP N RGD:5509061 20220811 MGI PMID:35789858 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20231123 MGI PMID:35840571 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210520 MGI 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0004844 abnormal vestibuloocular reflex IAGP N RGD:5509061 20220811 MGI PMID:35789858 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210520 MGI 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20220811 MGI PMID:35789858 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20231123 MGI PMID:35840571 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20231123 MGI PMID:35840571 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20220811 MGI PMID:35789858 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20220811 MGI PMID:35789858 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20231123 MGI PMID:35840571 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20231123 MGI PMID:35840571 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0020379 abnormal sucrose solution preference IAGP N RGD:5509061 20220811 MGI PMID:35789858 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20231123 MGI PMID:35840571 1557207 Slitrk2 SLIT and NTRK-like family, member 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1557208 Cd177 CD177 antigen gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20160324 MGI PMID:25359465 1557208 Cd177 CD177 antigen gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20160324 MGI PMID:25359465 1557208 Cd177 CD177 antigen gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20160324 MGI PMID:25359465 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20170105 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20160804 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0000745 tremors IEA N RGD:5509061 20200402 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0002608 increased hematocrit IEA N RGD:5509061 20210128 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20181227 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160114 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20160114 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0003443 increased circulating glycerol level IEA N RGD:5509061 20211021 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20170105 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200402 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20170105 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0005014 increased B cell number IEA N RGD:5509061 20160804 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20160114 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160114 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160114 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20181227 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20201231 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0008210 increased mature B cell number IEA N RGD:5509061 20160804 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0008347 decreased gamma-delta T cell number IEA N RGD:5509061 20160804 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20160114 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200402 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0010851 decreased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20190711 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0012767 increased KLRG1-positive NK cell number IEA N RGD:5509061 20160804 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0013022 increased Ly6C high monocyte number IEA N RGD:5509061 20160804 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0013025 increased Ly6C low monocyte number IEA N RGD:5509061 20160804 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:23851121 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0013513 decreased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0013519 decreased CD4-positive NK T cell number IEA N RGD:5509061 20201231 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0013522 decreased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20201231 MGI 1557209 Clpp caseinolytic mitochondrial matrix peptidase proteolytic subunit gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20190711 MGI PMID:23851121 1557210 Fn3k fructosamine 3 kinase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16819943 1557210 Fn3k fructosamine 3 kinase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16819943 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0000610 cholestasis IAGP N RGD:5509061 20141003 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0000610 cholestasis IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0000746 weakness IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20141003 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0005284 increased saturated fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0006084 abnormal circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0010140 phlebitis IAGP N RGD:5509061 20201224 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0014010 abnormal peroxisome morphology IAGP N RGD:5509061 20200227 MGI PMID:31207289 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:24503136 1557211 Pex1 peroxisomal biogenesis factor 1 gene MP:0031158 abnormal venous thrombosis IAGP N RGD:5509061 20201224 MGI PMID:31207289 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10725384 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21546531 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20170126 MGI PMID:22563472 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20200109 MGI PMID:27162334 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:10725384 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:14691151 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20170126 MGI PMID:11853768 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20170126 MGI PMID:22563472 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:10725384 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:14691151 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0001326 retina degeneration IAGP N RGD:5509061 20150129 MGI PMID:22807293 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0001326 retina degeneration IAGP N RGD:5509061 20170126 MGI PMID:22563472 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:20007830 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20170126 MGI PMID:22563472 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20170126 MGI PMID:11853768 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20170126 MGI PMID:22563472 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20200109 MGI PMID:27162334 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20170126 MGI PMID:22563472 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:20007830 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:20007830 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21546531 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20007830 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20150129 MGI PMID:22807293 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20007830 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20150129 MGI PMID:22807293 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20170126 MGI PMID:22563472 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0004175 telangiectasia IAGP N RGD:5509061 20170126 MGI PMID:22563472 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20170126 MGI PMID:22563472 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:10725384 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:14691151 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:20007830 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12651948 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:20007830 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:10725384 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:12651948 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21546531 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12651948 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:10725384 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20170126 MGI PMID:22563472 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:10725384 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20007830 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20150129 MGI PMID:22807293 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20170126 MGI PMID:22563472 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20170126 MGI PMID:11853768 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20170126 MGI PMID:22563472 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:21546531 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:21546531 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:10725384 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:21546531 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20170126 MGI PMID:22563472 1557212 Rpgr retinitis pigmentosa GTPase regulator gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20170126 MGI PMID:22563472 1557213 Dtx3l deltex 3-like, E3 ubiquitin ligase gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1557213 Dtx3l deltex 3-like, E3 ubiquitin ligase gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220519 MGI 1557213 Dtx3l deltex 3-like, E3 ubiquitin ligase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1557213 Dtx3l deltex 3-like, E3 ubiquitin ligase gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1557213 Dtx3l deltex 3-like, E3 ubiquitin ligase gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210826 MGI 1557213 Dtx3l deltex 3-like, E3 ubiquitin ligase gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1557214 Trim39 tripartite motif-containing 39 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1557214 Trim39 tripartite motif-containing 39 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20200402 MGI 1557214 Trim39 tripartite motif-containing 39 gene MP:0001314 cornea opacity IEA N RGD:5509061 20201231 MGI 1557214 Trim39 tripartite motif-containing 39 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1557214 Trim39 tripartite motif-containing 39 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1557214 Trim39 tripartite motif-containing 39 gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 1557214 Trim39 tripartite motif-containing 39 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20181227 MGI 1557214 Trim39 tripartite motif-containing 39 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1557214 Trim39 tripartite motif-containing 39 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20230601 MGI 1557214 Trim39 tripartite motif-containing 39 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20201022 MGI 1557214 Trim39 tripartite motif-containing 39 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1557214 Trim39 tripartite motif-containing 39 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1557215 Hoxd3 homeobox D3 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557215 Hoxd3 homeobox D3 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9520319 1557215 Hoxd3 homeobox D3 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:10688203 1557215 Hoxd3 homeobox D3 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:7913519 1557215 Hoxd3 homeobox D3 gene MP:0001051 abnormal somatic motor system morphology IAGP N RGD:5509061 20141003 MGI PMID:12954718 1557215 Hoxd3 homeobox D3 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7910549 1557215 Hoxd3 homeobox D3 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10688203 1557215 Hoxd3 homeobox D3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557215 Hoxd3 homeobox D3 gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7913519 1557215 Hoxd3 homeobox D3 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20141003 MGI PMID:9520319 1557215 Hoxd3 homeobox D3 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7910549 1557215 Hoxd3 homeobox D3 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7913519 1557215 Hoxd3 homeobox D3 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557215 Hoxd3 homeobox D3 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10688203 1557215 Hoxd3 homeobox D3 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557215 Hoxd3 homeobox D3 gene MP:0003955 abnormal ultimobranchial body morphology IAGP N RGD:5509061 20141003 MGI PMID:9520319 1557215 Hoxd3 homeobox D3 gene MP:0004568 fusion of glossopharyngeal and vagus nerve IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557215 Hoxd3 homeobox D3 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:10688203 1557215 Hoxd3 homeobox D3 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:7910549 1557215 Hoxd3 homeobox D3 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:7913519 1557215 Hoxd3 homeobox D3 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:7910549 1557215 Hoxd3 homeobox D3 gene MP:0004659 abnormal odontoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:10688203 1557215 Hoxd3 homeobox D3 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12954718 1557215 Hoxd3 homeobox D3 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:7910549 1557215 Hoxd3 homeobox D3 gene MP:0009879 abnormal arcus anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:10688203 1557215 Hoxd3 homeobox D3 gene MP:0009899 hyoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7913519 1557215 Hoxd3 homeobox D3 gene MP:0010701 fusion of atlas and odontoid process IAGP N RGD:5509061 20141003 MGI PMID:10688203 1557215 Hoxd3 homeobox D3 gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20141003 MGI PMID:7910549 1557215 Hoxd3 homeobox D3 gene MP:0010729 absent arcus anterior IAGP N RGD:5509061 20141003 MGI PMID:10688203 1557215 Hoxd3 homeobox D3 gene MP:0010730 absent odontoid process IAGP N RGD:5509061 20141003 MGI PMID:10688203 1557215 Hoxd3 homeobox D3 gene MP:0010730 absent odontoid process IAGP N RGD:5509061 20141003 MGI PMID:7910549 1557215 Hoxd3 homeobox D3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557215 Hoxd3 homeobox D3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7910549 1557215 Hoxd3 homeobox D3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557215 Hoxd3 homeobox D3 gene MP:0011513 abnormal vertebral artery morphology IAGP N RGD:5509061 20141003 MGI PMID:7910549 1557215 Hoxd3 homeobox D3 gene MP:0011576 absent cervical atlas IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557215 Hoxd3 homeobox D3 gene MP:0011576 absent cervical atlas IAGP N RGD:5509061 20141003 MGI PMID:7913519 1557215 Hoxd3 homeobox D3 gene MP:0013290 persistent ultimobranchial bodies IAGP N RGD:5509061 20150122 MGI PMID:9520319 1557215 Hoxd3 homeobox D3 gene MP:0013574 ectopic parathyroid gland IAGP N RGD:5509061 20150305 MGI PMID:9520319 1557215 Hoxd3 homeobox D3 gene MP:0030871 abnormal inferior horn of thyroid cartilage morphology IAGP N RGD:5509061 20181101 MGI PMID:7913519 1557217 Gstm4 glutathione S-transferase, mu 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1557217 Gstm4 glutathione S-transferase, mu 4 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20191128 MGI 1557218 Eda2r ectodysplasin A2 receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14749376 1557219 Chst5 carbohydrate sulfotransferase 5 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:16938851 1557219 Chst5 carbohydrate sulfotransferase 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1557219 Chst5 carbohydrate sulfotransferase 5 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:16938851 1557219 Chst5 carbohydrate sulfotransferase 5 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20220811 MGI 1557219 Chst5 carbohydrate sulfotransferase 5 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:16938851 1557219 Chst5 carbohydrate sulfotransferase 5 gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20220811 MGI 1557219 Chst5 carbohydrate sulfotransferase 5 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:16938851 1557219 Chst5 carbohydrate sulfotransferase 5 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557220 Pml promyelocytic leukemia gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20180830 MGI PMID:29191918 1557220 Pml promyelocytic leukemia gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9488655 1557220 Pml promyelocytic leukemia gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20230615 MGI PMID:23656786 1557220 Pml promyelocytic leukemia gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:9488655 1557220 Pml promyelocytic leukemia gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21364283 1557220 Pml promyelocytic leukemia gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180830 MGI PMID:29191918 1557220 Pml promyelocytic leukemia gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9488655 1557220 Pml promyelocytic leukemia gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230615 MGI PMID:23656786 1557220 Pml promyelocytic leukemia gene MP:0001577 anemia IAGP N RGD:5509061 20180830 MGI PMID:29191918 1557220 Pml promyelocytic leukemia gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9488655 1557220 Pml promyelocytic leukemia gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9488655 1557220 Pml promyelocytic leukemia gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20180830 MGI PMID:29191918 1557220 Pml promyelocytic leukemia gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20230615 MGI PMID:23656786 1557220 Pml promyelocytic leukemia gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20180830 MGI PMID:29191918 1557220 Pml promyelocytic leukemia gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20230615 MGI PMID:23656786 1557220 Pml promyelocytic leukemia gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21364283 1557220 Pml promyelocytic leukemia gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20230615 MGI PMID:23656786 1557220 Pml promyelocytic leukemia gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20230615 MGI PMID:23656786 1557220 Pml promyelocytic leukemia gene MP:0002083 premature death IAGP N RGD:5509061 20230615 MGI PMID:23656786 1557220 Pml promyelocytic leukemia gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21364283 1557220 Pml promyelocytic leukemia gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9488655 1557220 Pml promyelocytic leukemia gene MP:0003701 elevated level of mitotic sister chromatid exchange IAGP N RGD:5509061 20180830 MGI PMID:29191918 1557220 Pml promyelocytic leukemia gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230615 MGI PMID:23656786 1557220 Pml promyelocytic leukemia gene MP:0004049 increased acute promyelocytic leukemia incidence IAGP N RGD:5509061 20180830 MGI PMID:29191918 1557220 Pml promyelocytic leukemia gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20180830 MGI PMID:29191918 1557220 Pml promyelocytic leukemia gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20180830 MGI PMID:29191918 1557220 Pml promyelocytic leukemia gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21364283 1557220 Pml promyelocytic leukemia gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20180830 MGI PMID:29191918 1557220 Pml promyelocytic leukemia gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9488655 1557220 Pml promyelocytic leukemia gene MP:0008886 abnormal PML bodies IAGP N RGD:5509061 20180830 MGI PMID:29191918 1557220 Pml promyelocytic leukemia gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21364283 1557220 Pml promyelocytic leukemia gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20180830 MGI PMID:29191918 1557220 Pml promyelocytic leukemia gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21364283 1557220 Pml promyelocytic leukemia gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20230615 MGI PMID:23656786 1557220 Pml promyelocytic leukemia gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:9488655 1557220 Pml promyelocytic leukemia gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9488655 1557220 Pml promyelocytic leukemia gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20230615 MGI PMID:23656786 1557220 Pml promyelocytic leukemia gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230615 MGI PMID:23656786 1557220 Pml promyelocytic leukemia gene MP:0031058 hepatosplenomegaly IAGP N RGD:5509061 20230615 MGI PMID:23656786 1557223 Atp11b ATPase, class VI, type 11B gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210520 MGI 1557223 Atp11b ATPase, class VI, type 11B gene MP:0004832 enlarged ovary IEA N RGD:5509061 20220519 MGI 1557223 Atp11b ATPase, class VI, type 11B gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1557223 Atp11b ATPase, class VI, type 11B gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220519 MGI 1557224 Atg3 autophagy related 3 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:21421856 1557224 Atg3 autophagy related 3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:21421856 1557224 Atg3 autophagy related 3 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:21421856 1557224 Atg3 autophagy related 3 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21421856 1557224 Atg3 autophagy related 3 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20200310 MGI PMID:18768753 1557224 Atg3 autophagy related 3 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:21421856 1557224 Atg3 autophagy related 3 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:21421856 1557224 Atg3 autophagy related 3 gene MP:0008071 absent B cells IAGP N RGD:5509061 20200310 MGI PMID:27303042 1557224 Atg3 autophagy related 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:21421856 1557224 Atg3 autophagy related 3 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:21421856 1557224 Atg3 autophagy related 3 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20200310 MGI PMID:18768753 1557224 Atg3 autophagy related 3 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20200310 MGI PMID:27303042 1557224 Atg3 autophagy related 3 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20200310 MGI PMID:18768753 1557224 Atg3 autophagy related 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:18768753 1557224 Atg3 autophagy related 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18768753 1557224 Atg3 autophagy related 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557224 Atg3 autophagy related 3 gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20200310 MGI PMID:18768753 1557224 Atg3 autophagy related 3 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200310 MGI PMID:21421856 1557225 Ddx19b DEAD box helicase 19b gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1557225 Ddx19b DEAD box helicase 19b gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20210506 MGI PMID:30699353 1557225 Ddx19b DEAD box helicase 19b gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210506 MGI PMID:30699353 1557225 Ddx19b DEAD box helicase 19b gene MP:0008562 increased interferon-alpha secretion IAGP N RGD:5509061 20210506 MGI PMID:30699353 1557225 Ddx19b DEAD box helicase 19b gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20210506 MGI PMID:30699353 1557225 Ddx19b DEAD box helicase 19b gene MP:0009198 abnormal male genitalia morphology IEA N RGD:5509061 20230720 MGI 1557225 Ddx19b DEAD box helicase 19b gene MP:0010768 mortality/aging IAGP N RGD:5509061 20210506 MGI PMID:30699353 1557225 Ddx19b DEAD box helicase 19b gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210506 MGI PMID:30699353 1557226 Ecsit ECSIT signalling integrator gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14633973 1557226 Ecsit ECSIT signalling integrator gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:14633973 1557226 Ecsit ECSIT signalling integrator gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:14633973 1557226 Ecsit ECSIT signalling integrator gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14633973 1557226 Ecsit ECSIT signalling integrator gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20160929 MGI PMID:27534441 1557226 Ecsit ECSIT signalling integrator gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14633973 1557226 Ecsit ECSIT signalling integrator gene MP:0011190 thick embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:14633973 1557227 Heatr5b HEAT repeat containing 5B gene MP:0014257 embryonic lethality prior to tooth bud stage, complete penetrance IAGP N RGD:5509061 20231102 MGI PMID:33824466 1557228 Col20a1 collagen, type XX, alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1557230 Mospd1 motile sperm domain containing 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1557231 Styk1 serine/threonine/tyrosine kinase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:30758858 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20170504 MGI 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0001523 impaired righting response IEA N RGD:5509061 20170504 MGI 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20220811 MGI PMID:35358843 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20220811 MGI PMID:35358843 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0002083 premature death IAGP N RGD:5509061 20220811 MGI PMID:35358843 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20220811 MGI PMID:35358843 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20220811 MGI PMID:35358843 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20220811 MGI PMID:35358843 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20220811 MGI PMID:35358843 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20220811 MGI PMID:35358843 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20220811 MGI PMID:35358843 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20220811 MGI PMID:35358843 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20220811 MGI PMID:35358843 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20220811 MGI PMID:35358843 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20220811 MGI PMID:35358843 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20211021 MGI 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20220811 MGI PMID:35358843 1557234 Slc8b1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:35358843 1557237 Neurl3 neuralized E3 ubiquitin protein ligase 3 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20240620 MGI PMID:35792897 1557237 Neurl3 neuralized E3 ubiquitin protein ligase 3 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20240620 MGI PMID:35792897 1557237 Neurl3 neuralized E3 ubiquitin protein ligase 3 gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20240620 MGI PMID:35792897 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20141003 MGI 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20160804 MGI 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0003345 decreased rib number IEA N RGD:5509061 20141003 MGI 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20141003 MGI 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0004648 decreased thoracic vertebrae number IEA N RGD:5509061 20141003 MGI 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:22696294 1557238 Zc3hc1 zinc finger, C3HC type 1 gene MP:0031474 increased female germ cell apoptosis IAGP N RGD:5509061 20230615 MGI PMID:22696294 1557239 Crabp1 cellular retinoic acid binding protein I gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 1557239 Crabp1 cellular retinoic acid binding protein I gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:7768191 1557239 Crabp1 cellular retinoic acid binding protein I gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20181227 MGI 1557239 Crabp1 cellular retinoic acid binding protein I gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210128 MGI 1557239 Crabp1 cellular retinoic acid binding protein I gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7768191 1557239 Crabp1 cellular retinoic acid binding protein I gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7890139 1557239 Crabp1 cellular retinoic acid binding protein I gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8090764 1557239 Crabp1 cellular retinoic acid binding protein I gene MP:0004832 enlarged ovary IEA N RGD:5509061 20181227 MGI 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0000433 microcephaly IEA N RGD:5509061 20111116 MGI 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:22187431 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:19686682 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19686682 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:19686682 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:19686682 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19686682 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0001147 small testis IAGP N RGD:5509061 20220630 MGI PMID:29259204 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220630 MGI PMID:29259204 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22187431 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:22187431 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0001685 abnormal endoderm development IEA N RGD:5509061 20111116 MGI 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0001695 abnormal gastrulation IEA N RGD:5509061 20111116 MGI 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0001701 incomplete embryo turning IEA N RGD:5509061 20111116 MGI 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:22187431 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220630 MGI PMID:29259204 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19686682 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22187431 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0002084 abnormal developmental patterning IEA N RGD:5509061 20111116 MGI 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:19686682 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22187431 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0002188 small heart IEA N RGD:5509061 20111116 MGI 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20220630 MGI PMID:29259204 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220630 MGI PMID:29259204 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22187431 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:22187431 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20111116 MGI 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220630 MGI PMID:29259204 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220630 MGI PMID:29259204 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:19686682 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:19686682 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20220630 MGI PMID:29259204 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22187431 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22187431 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:19686682 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20220630 MGI PMID:29259204 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220630 MGI PMID:29259204 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0008203 absent B-1a cells IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:22187431 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:22213803 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20220630 MGI PMID:29259204 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220630 MGI PMID:29259204 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20220630 MGI PMID:29259204 1557240 Huwe1 HECT, UBA and WWE domain containing 1 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:22213803 1557241 Tmem120a transmembrane protein 120A gene MP:0020374 abnormal nocifensive behavior IAGP N RGD:5509061 20210204 MGI PMID:32084332 1557241 Tmem120a transmembrane protein 120A gene MP:0020955 increased mechanical nociceptive threshold IAGP N RGD:5509061 20210204 MGI PMID:32084332 1557242 Zfp706 zinc finger protein 706 gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1557242 Zfp706 zinc finger protein 706 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1557242 Zfp706 zinc finger protein 706 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1557242 Zfp706 zinc finger protein 706 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557243 Gpd1l glycerol-3-phosphate dehydrogenase 1-like gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1557244 Trim66 tripartite motif-containing 66 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1557244 Trim66 tripartite motif-containing 66 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20160804 MGI 1557244 Trim66 tripartite motif-containing 66 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20240627 MGI PMID:38719749 1557244 Trim66 tripartite motif-containing 66 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1557244 Trim66 tripartite motif-containing 66 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1557244 Trim66 tripartite motif-containing 66 gene MP:0010723 paternal effect IAGP N RGD:5509061 20240627 MGI PMID:38719749 1557244 Trim66 tripartite motif-containing 66 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240627 MGI PMID:38719749 1557246 Neurod6 neurogenic differentiation 6 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:10804213 1557246 Neurod6 neurogenic differentiation 6 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20181220 MGI PMID:29911180 1557246 Neurod6 neurogenic differentiation 6 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15314171 1557246 Neurod6 neurogenic differentiation 6 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20200827 MGI PMID:31780330 1557246 Neurod6 neurogenic differentiation 6 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21315259 1557246 Neurod6 neurogenic differentiation 6 gene MP:0000794 abnormal parietal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:22810622 1557246 Neurod6 neurogenic differentiation 6 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200827 MGI PMID:31780330 1557246 Neurod6 neurogenic differentiation 6 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:10804213 1557246 Neurod6 neurogenic differentiation 6 gene MP:0000861 disorganized barrel cortex IAGP N RGD:5509061 20141003 MGI PMID:16862160 1557246 Neurod6 neurogenic differentiation 6 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:21315259 1557246 Neurod6 neurogenic differentiation 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200827 MGI PMID:31780330 1557246 Neurod6 neurogenic differentiation 6 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:22153375 1557246 Neurod6 neurogenic differentiation 6 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200827 MGI PMID:31780330 1557246 Neurod6 neurogenic differentiation 6 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21885734 1557246 Neurod6 neurogenic differentiation 6 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21885734 1557246 Neurod6 neurogenic differentiation 6 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:22153375 1557246 Neurod6 neurogenic differentiation 6 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23785142 1557246 Neurod6 neurogenic differentiation 6 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12853418 1557246 Neurod6 neurogenic differentiation 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10804213 1557246 Neurod6 neurogenic differentiation 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16251442 1557246 Neurod6 neurogenic differentiation 6 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20200827 MGI PMID:31780330 1557246 Neurod6 neurogenic differentiation 6 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20200827 MGI PMID:31780330 1557246 Neurod6 neurogenic differentiation 6 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:21885734 1557246 Neurod6 neurogenic differentiation 6 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:10804213 1557246 Neurod6 neurogenic differentiation 6 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20200827 MGI PMID:31780330 1557246 Neurod6 neurogenic differentiation 6 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:16908411 1557246 Neurod6 neurogenic differentiation 6 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:22219273 1557246 Neurod6 neurogenic differentiation 6 gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:23785142 1557246 Neurod6 neurogenic differentiation 6 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:19607846 1557246 Neurod6 neurogenic differentiation 6 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:10804213 1557246 Neurod6 neurogenic differentiation 6 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:10804213 1557246 Neurod6 neurogenic differentiation 6 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:21050275 1557246 Neurod6 neurogenic differentiation 6 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:10804213 1557246 Neurod6 neurogenic differentiation 6 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:21315259 1557246 Neurod6 neurogenic differentiation 6 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:20159449 1557246 Neurod6 neurogenic differentiation 6 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20200827 MGI PMID:31780330 1557246 Neurod6 neurogenic differentiation 6 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:20159449 1557246 Neurod6 neurogenic differentiation 6 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:22219273 1557246 Neurod6 neurogenic differentiation 6 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557246 Neurod6 neurogenic differentiation 6 gene MP:0008285 abnormal hippocampus granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:10804213 1557246 Neurod6 neurogenic differentiation 6 gene MP:0008443 absent subplate IAGP N RGD:5509061 20141003 MGI PMID:21315259 1557246 Neurod6 neurogenic differentiation 6 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:20159449 1557246 Neurod6 neurogenic differentiation 6 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:21050275 1557246 Neurod6 neurogenic differentiation 6 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:22219273 1557246 Neurod6 neurogenic differentiation 6 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23785142 1557246 Neurod6 neurogenic differentiation 6 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22219273 1557246 Neurod6 neurogenic differentiation 6 gene MP:0010011 ectopic hippocampus pyramidal cells IAGP N RGD:5509061 20141003 MGI PMID:22219273 1557246 Neurod6 neurogenic differentiation 6 gene MP:0010011 ectopic hippocampus pyramidal cells IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557246 Neurod6 neurogenic differentiation 6 gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20141003 MGI PMID:19607846 1557246 Neurod6 neurogenic differentiation 6 gene MP:0010770 preweaning lethality IAGP N RGD:5509061 20200827 MGI PMID:31780330 1557246 Neurod6 neurogenic differentiation 6 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23522044 1557246 Neurod6 neurogenic differentiation 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10804213 1557246 Neurod6 neurogenic differentiation 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15314171 1557246 Neurod6 neurogenic differentiation 6 gene MP:0011150 abnormal hippocampus stratum oriens morphology IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557246 Neurod6 neurogenic differentiation 6 gene MP:0014375 increased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:31780330 1557246 Neurod6 neurogenic differentiation 6 gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:31780330 1557246 Neurod6 neurogenic differentiation 6 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20200827 MGI PMID:31780330 1557246 Neurod6 neurogenic differentiation 6 gene MP:0020507 increased dendritic spine density IAGP N RGD:5509061 20200827 MGI PMID:31780330 1557246 Neurod6 neurogenic differentiation 6 gene MP:0020594 decreased cerebral cortex cell number IAGP N RGD:5509061 20190215 MGI PMID:28288114 1557246 Neurod6 neurogenic differentiation 6 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22153375 1557248 Aoah acyloxyacyl hydrolase gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:12810692 1557249 Slc35f1 solute carrier family 35, member F1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160915 MGI PMID:24652767 1557249 Slc35f1 solute carrier family 35, member F1 gene MP:0005571 decreased lactate dehydrogenase level IEA N RGD:5509061 20160804 MGI 1557252 Ncoa7 nuclear receptor coactivator 7 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20210617 MGI PMID:33340069 1557252 Ncoa7 nuclear receptor coactivator 7 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20210617 MGI PMID:33340069 1557252 Ncoa7 nuclear receptor coactivator 7 gene MP:0001393 ataxia IAGP N RGD:5509061 20210617 MGI PMID:33340069 1557252 Ncoa7 nuclear receptor coactivator 7 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20231207 MGI 1557252 Ncoa7 nuclear receptor coactivator 7 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20210617 MGI PMID:33340069 1557252 Ncoa7 nuclear receptor coactivator 7 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20210617 MGI PMID:33340069 1557252 Ncoa7 nuclear receptor coactivator 7 gene MP:0009349 increased urine pH IAGP N RGD:5509061 20210617 MGI PMID:33340069 1557252 Ncoa7 nuclear receptor coactivator 7 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20210617 MGI PMID:33340069 1557252 Ncoa7 nuclear receptor coactivator 7 gene MP:0020358 abnormal inhibitory synapse morphology IAGP N RGD:5509061 20210617 MGI PMID:33340069 1557252 Ncoa7 nuclear receptor coactivator 7 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20210617 MGI PMID:33340069 1557254 Gpr160 G protein-coupled receptor 160 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1557254 Gpr160 G protein-coupled receptor 160 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1557254 Gpr160 G protein-coupled receptor 160 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1557256 Hcfc1 host cell factor C1 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20170615 MGI PMID:26921005 1557256 Hcfc1 host cell factor C1 gene MP:0000373 belly spot IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20220217 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20220721 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20220217 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0000592 short tail IAGP N RGD:5509061 20220721 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20170615 MGI PMID:26921005 1557256 Hcfc1 host cell factor C1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170615 MGI PMID:26921005 1557256 Hcfc1 host cell factor C1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20170615 MGI PMID:26921005 1557256 Hcfc1 host cell factor C1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20220217 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20170615 MGI PMID:26921005 1557256 Hcfc1 host cell factor C1 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0005352 small cranium IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20170615 MGI PMID:26921005 1557256 Hcfc1 host cell factor C1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20170615 MGI PMID:26921005 1557256 Hcfc1 host cell factor C1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0006411 upturned snout IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20220721 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20220217 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20170615 MGI PMID:26921005 1557256 Hcfc1 host cell factor C1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20220217 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20170615 MGI PMID:26921005 1557256 Hcfc1 host cell factor C1 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20170615 MGI PMID:26921005 1557256 Hcfc1 host cell factor C1 gene MP:0030066 short face IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0030630 increased circulating methylmalonic acid level IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557256 Hcfc1 host cell factor C1 gene MP:0030930 decreased digit pigmentation IAGP N RGD:5509061 20220210 MGI PMID:35013307 1557257 Sspo SCO-spondin gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210826 MGI 1557257 Sspo SCO-spondin gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1557257 Sspo SCO-spondin gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1557257 Sspo SCO-spondin gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20240307 MGI PMID:38049798 1557257 Sspo SCO-spondin gene MP:0013908 small lateral ventricles IAGP N RGD:5509061 20240307 MGI PMID:38049798 1557257 Sspo SCO-spondin gene MP:0013909 small third ventricle IAGP N RGD:5509061 20240307 MGI PMID:38049798 1557257 Sspo SCO-spondin gene MP:0014402 abnormal Reissner's fiber morphology IAGP N RGD:5509061 20240321 MGI PMID:38049798 1557259 Klhl4 kelch-like 4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20190725 MGI 1557260 Rasgef1b RasGEF domain family, member 1B gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1557260 Rasgef1b RasGEF domain family, member 1B gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1557260 Rasgef1b RasGEF domain family, member 1B gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1557261 Akr1c19 aldo-keto reductase family 1, member C19 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240222 MGI PMID:34843575 1557261 Akr1c19 aldo-keto reductase family 1, member C19 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20230601 MGI 1557261 Akr1c19 aldo-keto reductase family 1, member C19 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1557262 Garnl3 GTPase activating RANGAP domain-like 3 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1557266 Tmc7 transmembrane channel-like gene family 7 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1557266 Tmc7 transmembrane channel-like gene family 7 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1557266 Tmc7 transmembrane channel-like gene family 7 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1557266 Tmc7 transmembrane channel-like gene family 7 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 1557266 Tmc7 transmembrane channel-like gene family 7 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1557266 Tmc7 transmembrane channel-like gene family 7 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1557266 Tmc7 transmembrane channel-like gene family 7 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1557266 Tmc7 transmembrane channel-like gene family 7 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1557266 Tmc7 transmembrane channel-like gene family 7 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1557266 Tmc7 transmembrane channel-like gene family 7 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1557267 Nobox NOBOX oogenesis homeobox gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15326356 1557267 Nobox NOBOX oogenesis homeobox gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:15326356 1557267 Nobox NOBOX oogenesis homeobox gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1557267 Nobox NOBOX oogenesis homeobox gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1557267 Nobox NOBOX oogenesis homeobox gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15326356 1557267 Nobox NOBOX oogenesis homeobox gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:15326356 1557267 Nobox NOBOX oogenesis homeobox gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20160811 MGI 1557267 Nobox NOBOX oogenesis homeobox gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1557267 Nobox NOBOX oogenesis homeobox gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:15326356 1557267 Nobox NOBOX oogenesis homeobox gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:15326356 1557267 Nobox NOBOX oogenesis homeobox gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:15326356 1557267 Nobox NOBOX oogenesis homeobox gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:15326356 1557267 Nobox NOBOX oogenesis homeobox gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:15326356 1557267 Nobox NOBOX oogenesis homeobox gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20160421 MGI 1557267 Nobox NOBOX oogenesis homeobox gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1557267 Nobox NOBOX oogenesis homeobox gene MP:0031382 absent secondary ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:15326356 1557268 Psd3 pleckstrin and Sec7 domain containing 3 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20230601 MGI 1557268 Psd3 pleckstrin and Sec7 domain containing 3 gene MP:0000745 tremors IEA N RGD:5509061 20200514 MGI 1557268 Psd3 pleckstrin and Sec7 domain containing 3 gene MP:0003394 increased cardiac output IEA N RGD:5509061 20230601 MGI 1557268 Psd3 pleckstrin and Sec7 domain containing 3 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20240523 MGI 1557268 Psd3 pleckstrin and Sec7 domain containing 3 gene MP:0009456 impaired cued conditioning behavior IEA N RGD:5509061 20230601 MGI 1557268 Psd3 pleckstrin and Sec7 domain containing 3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230601 MGI 1557268 Psd3 pleckstrin and Sec7 domain containing 3 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20211021 MGI 1557268 Psd3 pleckstrin and Sec7 domain containing 3 gene MP:0011951 increased cardiac stroke volume IEA N RGD:5509061 20230601 MGI 1557268 Psd3 pleckstrin and Sec7 domain containing 3 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0001127 small ovary IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:24155305 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:24155305 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:24155305 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:24155305 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24155305 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:24155305 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:24155305 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:24155305 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:24155305 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24155305 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0031018 decreased granulosa cell proliferation IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220505 MGI PMID:34930897 1557269 Cpeb3 cytoplasmic polyadenylation element binding protein 3 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:34930897 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18654663 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151231 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18654663 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18654663 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0003213 decreased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:18654663 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230601 MGI 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:18654663 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:18654663 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18654663 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005331 insulin resistance IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18654663 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:18654663 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18654663 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:18654663 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20210128 MGI 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18654663 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:18654663 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0011019 abnormal adaptive thermogenesis IAGP N RGD:5509061 20160128 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:18682832 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:25477509 1557270 Cidec cell death-inducing DFFA-like effector c gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:18654663 1557271 Dtx3 deltex 3, E3 ubiquitin ligase gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1557272 Tfdp1 transcription factor Dp 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12588846 1557272 Tfdp1 transcription factor Dp 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12588846 1557272 Tfdp1 transcription factor Dp 1 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:12588846 1557272 Tfdp1 transcription factor Dp 1 gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:12588846 1557272 Tfdp1 transcription factor Dp 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12588846 1557272 Tfdp1 transcription factor Dp 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12588846 1557272 Tfdp1 transcription factor Dp 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12588846 1557272 Tfdp1 transcription factor Dp 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12588846 1557272 Tfdp1 transcription factor Dp 1 gene MP:0012131 small visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:12588846 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000023 abnormal ear position IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:1018005 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23303524 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:15384171 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:23303524 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20171123 MGI PMID:1018005 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:10861288 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:10942421 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:15384171 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:16589192 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:10861288 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:10942421 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:16589192 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20221117 MGI PMID:15450095 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:1018005 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10861288 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000919 cranioschisis IAGP N RGD:5509061 20141003 MGI PMID:1018005 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000919 cranioschisis IAGP N RGD:5509061 20141003 MGI PMID:10861288 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:1018005 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10861288 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20221117 MGI PMID:15450095 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:10861288 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:23303524 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:23303524 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15384171 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:23303524 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10861288 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:10861288 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16589192 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16589192 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23303524 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23303524 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0002767 situs ambiguus IAGP N RGD:5509061 20141003 MGI PMID:10942421 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:23471918 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20160331 MGI PMID:23471918 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:23303524 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0004131 abnormal motile primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:23303524 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:23471918 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0004559 small allantois IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0004713 split notochord IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0005034 abnormal anus morphology IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0005224 abnormal left-right axis symmetry of the somites IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0006063 abnormal inferior vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0008533 abnormal anterior visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0008818 abnormal interfrontal bone morphology IAGP N RGD:5509061 20171123 MGI PMID:1018005 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0009916 absent hyoid bone greater horns IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0009959 abnormal cerebellar hemisphere morphology IAGP N RGD:5509061 20221117 MGI PMID:15450095 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0009990 abnormal cerebellum vermis lobule III morphology IAGP N RGD:5509061 20221117 MGI PMID:15450095 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0009993 abnormal cerebellum vermis lobule V morphology IAGP N RGD:5509061 20221117 MGI PMID:15450095 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0010807 abnormal stomach position or orientation IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0010853 abnormal lung position or orientation IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0010854 lung situs inversus IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0010854 lung situs inversus IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0011042 abnormal horizontal vestibuloocular reflex IAGP N RGD:5509061 20221117 MGI PMID:15450095 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10861288 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23184148 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0011660 ectopia cordis IAGP N RGD:5509061 20141003 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0011665 d-loop transposition of the great arteries IAGP N RGD:5509061 20240118 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0012156 rostral-caudal axis duplication IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0012739 abnormal anterior primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:16397896 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0020530 disorganized thalamus IAGP N RGD:5509061 20180208 MGI PMID:11959836 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0030100 hemifacial hypoplasia IAGP N RGD:5509061 20170928 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0030285 mandibular coronoid process hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0031345 developmental cataract IAGP N RGD:5509061 20220217 MGI PMID:17127413 1557273 Zic3 zinc finger protein of the cerebellum 3 gene MP:0031392 hypoactivity IAGP N RGD:5509061 20221117 MGI PMID:15450095 1557277 Cbln3 cerebellin 3 precursor protein gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557277 Cbln3 cerebellin 3 precursor protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557277 Cbln3 cerebellin 3 precursor protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557277 Cbln3 cerebellin 3 precursor protein gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557277 Cbln3 cerebellin 3 precursor protein gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557277 Cbln3 cerebellin 3 precursor protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557277 Cbln3 cerebellin 3 precursor protein gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557277 Cbln3 cerebellin 3 precursor protein gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20141003 MGI PMID:17030622 1557277 Cbln3 cerebellin 3 precursor protein gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1557277 Cbln3 cerebellin 3 precursor protein gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20211021 MGI 1557278 Repin1 replication initiator 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170713 MGI PMID:27402271 1557278 Repin1 replication initiator 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20170713 MGI PMID:27402271 1557278 Repin1 replication initiator 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20170713 MGI PMID:27402271 1557278 Repin1 replication initiator 1 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20170713 MGI PMID:27402271 1557278 Repin1 replication initiator 1 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20170713 MGI PMID:27402271 1557279 Pabpn1l poly(A)binding protein nuclear 1-like gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20210429 MGI PMID:32558204 1557279 Pabpn1l poly(A)binding protein nuclear 1-like gene MP:0001926 female infertility IAGP N RGD:5509061 20210429 MGI PMID:32558204 1557279 Pabpn1l poly(A)binding protein nuclear 1-like gene MP:0003718 maternal effect IAGP N RGD:5509061 20210429 MGI PMID:32558204 1557280 Supt5 suppressor of Ty 5, DSIF elongation factor subunit gene MP:0003036 vertebral transformation IEA N RGD:5509061 20160114 MGI 1557280 Supt5 suppressor of Ty 5, DSIF elongation factor subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557280 Supt5 suppressor of Ty 5, DSIF elongation factor subunit gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20220224 MGI PMID:29514850 1557282 Dmkn dermokine gene MP:0001192 scaly skin IAGP N RGD:5509061 20191010 MGI PMID:24794495 1557282 Dmkn dermokine gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20191010 MGI PMID:24794495 1557282 Dmkn dermokine gene MP:0009605 decreased keratohyalin granule number IAGP N RGD:5509061 20191010 MGI PMID:24794495 1557282 Dmkn dermokine gene MP:0009607 decreased keratohyalin granule size IAGP N RGD:5509061 20191010 MGI PMID:24794495 1557283 Otud1 OTU domain containing 1 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20220901 MGI PMID:32075857 1557283 Otud1 OTU domain containing 1 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20220901 MGI PMID:32075857 1557283 Otud1 OTU domain containing 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20220901 MGI PMID:32075857 1557283 Otud1 OTU domain containing 1 gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20220901 MGI PMID:32075857 1557283 Otud1 OTU domain containing 1 gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20220901 MGI PMID:32075857 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:20589882 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20181227 MGI 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20160811 MGI 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20181227 MGI 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20181227 MGI 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0000897 abnormal midbrain morphology IEA N RGD:5509061 20181227 MGI 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15640247 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20589882 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22045912 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0001341 absent eyelids IAGP N RGD:5509061 20141003 MGI PMID:15640247 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20221215 MGI 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20589882 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22045912 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:22045912 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20170105 MGI 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0004156 abnormal QT variability IEA N RGD:5509061 20220519 MGI 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15640247 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1557284 Cecr2 CECR2, histone acetyl-lysine reader gene MP:0012260 encephalomeningocele IAGP N RGD:5509061 20141003 MGI PMID:20589882 1557286 Nags N-acetylglutamate synthase gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:22503289 1557286 Nags N-acetylglutamate synthase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22503289 1557286 Nags N-acetylglutamate synthase gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:22503289 1557286 Nags N-acetylglutamate synthase gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:22503289 1557286 Nags N-acetylglutamate synthase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:22503289 1557286 Nags N-acetylglutamate synthase gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22503289 1557286 Nags N-acetylglutamate synthase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22503289 1557286 Nags N-acetylglutamate synthase gene MP:0020837 decreased circulating citrulline level IAGP N RGD:5509061 20180712 MGI PMID:22503289 1557288 Cenpv centromere protein V gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1557288 Cenpv centromere protein V gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220106 MGI PMID:34764261 1557288 Cenpv centromere protein V gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20220106 MGI PMID:34764261 1557288 Cenpv centromere protein V gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20220106 MGI PMID:34764261 1557288 Cenpv centromere protein V gene MP:0014443 impaired polar body extrusion IAGP N RGD:5509061 20240509 MGI PMID:34764261 1557290 Myo3a myosin IIIA gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1557290 Myo3a myosin IIIA gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21165622 1557290 Myo3a myosin IIIA gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:21165622 1557290 Myo3a myosin IIIA gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21165622 1557290 Myo3a myosin IIIA gene MP:0004408 decreased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:21165622 1557290 Myo3a myosin IIIA gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1557290 Myo3a myosin IIIA gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1557290 Myo3a myosin IIIA gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:21165622 1557290 Myo3a myosin IIIA gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240321 MGI PMID:26926603 1557290 Myo3a myosin IIIA gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0001263 weight loss IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0001393 ataxia IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0003354 astrocytosis IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0005333 decreased heart rate IEA N RGD:5509061 20221215 MGI 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0005405 axon degeneration IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20231207 MGI 1557291 Spg11 SPG11, spatacsin vesicle trafficking associated gene MP:0012506 brain atrophy IAGP N RGD:5509061 20160915 MGI PMID:26284655 1557292 Zcchc13 zinc finger, CCHC domain containing 13 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:19004851 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:24086156 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20171116 MGI PMID:27009049 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19004851 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:19004851 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20171116 MGI PMID:27009049 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20171116 MGI PMID:27009049 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:24086156 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:19004851 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0001406 abnormal gait IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0001925 male infertility IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0001926 female infertility IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20231207 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20171116 MGI PMID:27009049 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20171116 MGI PMID:27009049 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20171116 MGI PMID:27009049 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:24086156 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:19004851 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0003164 decreased posterior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:24086156 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20171116 MGI PMID:27009049 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20171116 MGI PMID:27009049 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20171116 MGI PMID:27009049 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20141003 MGI PMID:19004851 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0004425 abnormal otolith organ morphology IAGP N RGD:5509061 20141003 MGI PMID:24086156 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:19004851 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:24086156 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24086156 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0011238 abnormal inner ear development IAGP N RGD:5509061 20141003 MGI PMID:24086156 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20171116 MGI PMID:27009049 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0011971 increased circulating lactate dehydrogenase level IEA N RGD:5509061 20230601 MGI 1557293 Lrig3 leucine-rich repeats and immunoglobulin-like domains 3 gene MP:0020204 abnormal heart left ventricle weight IAGP N RGD:5509061 20171116 MGI PMID:27009049 1557295 2810408A11Rik RIKEN cDNA 2810408A11 gene gene MP:0001260 increased body weight IEA N RGD:5509061 20141003 MGI 1557295 2810408A11Rik RIKEN cDNA 2810408A11 gene gene MP:0001513 limb grasping IEA N RGD:5509061 20141003 MGI 1557295 2810408A11Rik RIKEN cDNA 2810408A11 gene gene MP:0002833 increased heart weight IEA N RGD:5509061 20160804 MGI 1557295 2810408A11Rik RIKEN cDNA 2810408A11 gene gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1557295 2810408A11Rik RIKEN cDNA 2810408A11 gene gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160804 MGI 1557295 2810408A11Rik RIKEN cDNA 2810408A11 gene gene MP:0008044 increased NK cell number IEA N RGD:5509061 20141003 MGI 1557295 2810408A11Rik RIKEN cDNA 2810408A11 gene gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20160804 MGI 1557295 2810408A11Rik RIKEN cDNA 2810408A11 gene gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20141003 MGI 1557297 Rhox9 reproductive homeobox 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11689708 1557300 Actr3b ARP3 actin-related protein 3B gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1557300 Actr3b ARP3 actin-related protein 3B gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20240523 MGI 1557301 Bcor BCL6 interacting corepressor gene MP:0000088 short mandible IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0000111 cleft palate IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0000160 kyphosis IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20171207 MGI PMID:26847029 1557301 Bcor BCL6 interacting corepressor gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20111116 MGI 1557301 Bcor BCL6 interacting corepressor gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20171207 MGI PMID:26847029 1557301 Bcor BCL6 interacting corepressor gene MP:0000433 microcephaly IEA N RGD:5509061 20111116 MGI 1557301 Bcor BCL6 interacting corepressor gene MP:0000564 syndactyly IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0000585 kinked tail IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0001304 cataract IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0001689 incomplete somite formation IEA N RGD:5509061 20111116 MGI 1557301 Bcor BCL6 interacting corepressor gene MP:0001695 abnormal gastrulation IEA N RGD:5509061 20111116 MGI 1557301 Bcor BCL6 interacting corepressor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20111116 MGI 1557301 Bcor BCL6 interacting corepressor gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0002084 abnormal developmental patterning IEA N RGD:5509061 20111116 MGI 1557301 Bcor BCL6 interacting corepressor gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20111116 MGI 1557301 Bcor BCL6 interacting corepressor gene MP:0003717 pallor IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0003792 abnormal major salivary gland morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0004251 failure of heart looping IEA N RGD:5509061 20111116 MGI 1557301 Bcor BCL6 interacting corepressor gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0008862 asymmetric snout IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20171207 MGI PMID:26847029 1557301 Bcor BCL6 interacting corepressor gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0009909 bifid tongue IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IEA N RGD:5509061 20111116 MGI 1557301 Bcor BCL6 interacting corepressor gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0013264 tongue ankylosis IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0030189 broad snout IAGP N RGD:5509061 20221020 MGI PMID:32692983 1557301 Bcor BCL6 interacting corepressor gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:32692983 1557303 Supt7l SPT7-like, STAGA complex gamma subunit gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1557303 Supt7l SPT7-like, STAGA complex gamma subunit gene MP:0002074 abnormal hair texture IEA N RGD:5509061 20160804 MGI 1557303 Supt7l SPT7-like, STAGA complex gamma subunit gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1557303 Supt7l SPT7-like, STAGA complex gamma subunit gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1557305 Serpinb3a serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 3A gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:21126757 1557305 Serpinb3a serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 3A gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:21126757 1557305 Serpinb3a serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 3A gene MP:0010862 decreased respiratory mucosa goblet cell number IAGP N RGD:5509061 20141003 MGI PMID:21126757 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0001200 thick skin IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0001258 decreased body length IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0001258 decreased body length IAGP N RGD:5509061 20211104 MGI PMID:34424262 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20211104 MGI PMID:34424262 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20211104 MGI PMID:34424262 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20211104 MGI PMID:34424262 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0009405 increased skeletal muscle fiber number IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0011159 abnormal epidermal-dermal junction morphology IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20211104 MGI PMID:34424262 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0014164 abnormal ciliary process morphology IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0014176 abnormal cilary zonule morphology IAGP N RGD:5509061 20181220 MGI PMID:30060141 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0014176 abnormal cilary zonule morphology IAGP N RGD:5509061 20211104 MGI PMID:34424262 1557306 Adamts10 ADAM metallopeptidase with thrombospondin type 1 motif 10 gene MP:0031212 decreased eye anterior chamber depth IAGP N RGD:5509061 20211104 MGI PMID:34424262 1557308 Dnajc27 DnaJ heat shock protein family (Hsp40) member C27 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20170314 MGI PMID:24746703 1557308 Dnajc27 DnaJ heat shock protein family (Hsp40) member C27 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20170314 MGI PMID:24746703 1557308 Dnajc27 DnaJ heat shock protein family (Hsp40) member C27 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20170314 MGI PMID:24746703 1557308 Dnajc27 DnaJ heat shock protein family (Hsp40) member C27 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1557310 Bhlhe23 basic helix-loop-helix family, member e23 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15363390 1557310 Bhlhe23 basic helix-loop-helix family, member e23 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15363390 1557310 Bhlhe23 basic helix-loop-helix family, member e23 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:15363390 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:20089971 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20089971 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:20089971 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000440 domed cranium IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:20089971 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000445 short snout IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:20089971 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:21214893 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000547 short limbs IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:21214893 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21214893 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0001258 decreased body length IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:20089971 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0002274 abnormal type I pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:21214893 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20089971 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:20089971 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:21214893 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:20089971 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20089971 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0008274 failure of bone ossification IAGP N RGD:5509061 20141003 MGI PMID:20089971 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:20089971 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20089971 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:20089971 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0010449 heart right ventricle outflow tract stenosis IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0010827 small lung saccule IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21214893 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19112494 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20089971 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0020138 delayed bone mineralization IAGP N RGD:5509061 20180517 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0030949 abnormal Golgi vesicle transport IAGP N RGD:5509061 20190725 MGI PMID:29180569 1557313 Trip11 thyroid hormone receptor interactor 11 gene MP:0030952 abnormal Golgi stack morphology IAGP N RGD:5509061 20190725 MGI PMID:29180569 1557314 Invs inversin gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:16325766 1557314 Invs inversin gene MP:0000542 left-sided isomerism IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:8480178 1557314 Invs inversin gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:9771707 1557314 Invs inversin gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:16325766 1557314 Invs inversin gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8480178 1557314 Invs inversin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8480178 1557314 Invs inversin gene MP:0001785 edema IEA N RGD:5509061 20230119 MGI 1557314 Invs inversin gene MP:0001914 hemorrhage IEA N RGD:5509061 20230119 MGI 1557314 Invs inversin gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8480178 1557314 Invs inversin gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9771707 1557314 Invs inversin gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:8480178 1557314 Invs inversin gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:8480178 1557314 Invs inversin gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:9771707 1557314 Invs inversin gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:8480178 1557314 Invs inversin gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:9744276 1557314 Invs inversin gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:9771707 1557314 Invs inversin gene MP:0002767 situs ambiguus IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:16325766 1557314 Invs inversin gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12386294 1557314 Invs inversin gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:9744276 1557314 Invs inversin gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:10549278 1557314 Invs inversin gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:16325766 1557314 Invs inversin gene MP:0004159 double aortic arch IAGP N RGD:5509061 20141003 MGI PMID:16325766 1557314 Invs inversin gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:8480178 1557314 Invs inversin gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20141003 MGI PMID:9771707 1557314 Invs inversin gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:8480178 1557314 Invs inversin gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:9744276 1557314 Invs inversin gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:9771707 1557314 Invs inversin gene MP:0005083 abnormal biliary tract morphology IAGP N RGD:5509061 20141003 MGI PMID:9771707 1557314 Invs inversin gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:9771707 1557314 Invs inversin gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:8480178 1557314 Invs inversin gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9771707 1557314 Invs inversin gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0006062 abnormal vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0008461 left atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0008933 abnormal motile primary cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:10549278 1557314 Invs inversin gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:9771707 1557314 Invs inversin gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:9771707 1557314 Invs inversin gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9771707 1557314 Invs inversin gene MP:0009149 decreased pancreatic acinar cell number IAGP N RGD:5509061 20141003 MGI PMID:9771707 1557314 Invs inversin gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:9771707 1557314 Invs inversin gene MP:0010431 atrial situs inversus IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0010541 aorta hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16325766 1557314 Invs inversin gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:16325766 1557314 Invs inversin gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0010854 lung situs inversus IAGP N RGD:5509061 20141003 MGI PMID:16325766 1557314 Invs inversin gene MP:0010854 lung situs inversus IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1557314 Invs inversin gene MP:0011250 abdominal situs ambiguus IAGP N RGD:5509061 20141003 MGI PMID:9664638 1557314 Invs inversin gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0011308 kidney corticomedullary cyst IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0011341 abnormal loop of Henle descending limb morphology IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0011344 abnormal loop of Henle ascending limb thick segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0011352 proximal convoluted tubule brush border loss IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0011425 abnormal kidney interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:15213262 1557314 Invs inversin gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:12386294 1557314 Invs inversin gene MP:0012027 abnormal embryonic cilium location or orientation IAGP N RGD:5509061 20141003 MGI PMID:10549278 1557315 Camk1d calcium/calmodulin-dependent protein kinase ID gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210520 MGI 1557315 Camk1d calcium/calmodulin-dependent protein kinase ID gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1557315 Camk1d calcium/calmodulin-dependent protein kinase ID gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1557315 Camk1d calcium/calmodulin-dependent protein kinase ID gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1557315 Camk1d calcium/calmodulin-dependent protein kinase ID gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1557315 Camk1d calcium/calmodulin-dependent protein kinase ID gene MP:0002834 decreased heart weight IEA N RGD:5509061 20201022 MGI 1557315 Camk1d calcium/calmodulin-dependent protein kinase ID gene MP:0003450 enlarged pancreas IEA N RGD:5509061 20210128 MGI 1557315 Camk1d calcium/calmodulin-dependent protein kinase ID gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1557315 Camk1d calcium/calmodulin-dependent protein kinase ID gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210520 MGI 1557315 Camk1d calcium/calmodulin-dependent protein kinase ID gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1557315 Camk1d calcium/calmodulin-dependent protein kinase ID gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1557316 Vps41 VPS41 HOPS complex subunit gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:22698281 1557316 Vps41 VPS41 HOPS complex subunit gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:22698281 1557316 Vps41 VPS41 HOPS complex subunit gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:22698281 1557316 Vps41 VPS41 HOPS complex subunit gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:22698281 1557316 Vps41 VPS41 HOPS complex subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22698281 1557316 Vps41 VPS41 HOPS complex subunit gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:22698281 1557316 Vps41 VPS41 HOPS complex subunit gene MP:0003895 increased ectoderm apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22698281 1557316 Vps41 VPS41 HOPS complex subunit gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:22698281 1557316 Vps41 VPS41 HOPS complex subunit gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22698281 1557316 Vps41 VPS41 HOPS complex subunit gene MP:0030951 abnormal endocytosis IAGP N RGD:5509061 20190725 MGI PMID:22698281 1557317 Nwd2 NACHT and WD repeat domain containing 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20210128 MGI 1557317 Nwd2 NACHT and WD repeat domain containing 2 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210128 MGI 1557317 Nwd2 NACHT and WD repeat domain containing 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20200514 MGI 1557317 Nwd2 NACHT and WD repeat domain containing 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20200514 MGI 1557317 Nwd2 NACHT and WD repeat domain containing 2 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20200514 MGI 1557317 Nwd2 NACHT and WD repeat domain containing 2 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20201022 MGI 1557318 Zfyve19 zinc finger, FYVE domain containing 19 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1557318 Zfyve19 zinc finger, FYVE domain containing 19 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20221215 MGI 1557318 Zfyve19 zinc finger, FYVE domain containing 19 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220519 MGI 1557318 Zfyve19 zinc finger, FYVE domain containing 19 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20220811 MGI 1557318 Zfyve19 zinc finger, FYVE domain containing 19 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220519 MGI 1557319 Diaph2 diaphanous related formin 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20111116 MGI 1557319 Diaph2 diaphanous related formin 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141225 MGI PMID:22246438 1557319 Diaph2 diaphanous related formin 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141225 MGI PMID:22246438 1557319 Diaph2 diaphanous related formin 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141225 MGI PMID:22246438 1557319 Diaph2 diaphanous related formin 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20201022 MGI 1557319 Diaph2 diaphanous related formin 2 gene MP:0001914 hemorrhage IEA N RGD:5509061 20111116 MGI 1557319 Diaph2 diaphanous related formin 2 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20111116 MGI 1557319 Diaph2 diaphanous related formin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141225 MGI PMID:22246438 1557319 Diaph2 diaphanous related formin 2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141225 MGI PMID:22246438 1557319 Diaph2 diaphanous related formin 2 gene MP:0005377 hearing/vestibular/ear phenotype IAGP N RGD:5509061 20230420 MGI PMID:36689403 1557319 Diaph2 diaphanous related formin 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141225 MGI PMID:22246438 1557319 Diaph2 diaphanous related formin 2 gene MP:0009949 abnormal olfactory bulb granule cell layer morphology IAGP N RGD:5509061 20141225 MGI PMID:22246438 1557321 Golt1a golgi transport 1A gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1557321 Golt1a golgi transport 1A gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1557321 Golt1a golgi transport 1A gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1557321 Golt1a golgi transport 1A gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210520 MGI 1557321 Golt1a golgi transport 1A gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 1557325 Ifne interferon epsilon gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:23449591 1557325 Ifne interferon epsilon gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23449591 1557325 Ifne interferon epsilon gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:23449591 1557325 Ifne interferon epsilon gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:23449591 1557326 Lypd6b LY6/PLAUR domain containing 6B gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20221215 MGI 1557326 Lypd6b LY6/PLAUR domain containing 6B gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1557326 Lypd6b LY6/PLAUR domain containing 6B gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210520 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20170105 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20170105 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210128 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20170105 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20211021 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20170105 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20210520 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20190919 MGI PMID:31276534 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20170105 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20231207 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20170105 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20210826 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20211021 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0010580 decreased heart left ventricle size IEA N RGD:5509061 20210520 MGI 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20190919 MGI PMID:31276534 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20190919 MGI PMID:31276534 1557328 Eftud2 elongation factor Tu GTP binding domain containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557329 Aqp12 aquaporin 12 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1557329 Aqp12 aquaporin 12 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19726746 1557329 Aqp12 aquaporin 12 gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20141003 MGI PMID:19726746 1557329 Aqp12 aquaporin 12 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1557329 Aqp12 aquaporin 12 gene MP:0009160 abnormal pancreatic acinar cell zymogen granule morphology IAGP N RGD:5509061 20141003 MGI PMID:19726746 1557330 Dnah17 dynein, axonemal, heavy chain 17 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210506 MGI PMID:31658987 1557330 Dnah17 dynein, axonemal, heavy chain 17 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1557330 Dnah17 dynein, axonemal, heavy chain 17 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20210506 MGI PMID:31658987 1557330 Dnah17 dynein, axonemal, heavy chain 17 gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20201022 MGI 1557330 Dnah17 dynein, axonemal, heavy chain 17 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210506 MGI PMID:31658987 1557330 Dnah17 dynein, axonemal, heavy chain 17 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20210506 MGI PMID:31658987 1557330 Dnah17 dynein, axonemal, heavy chain 17 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210506 MGI PMID:31658987 1557330 Dnah17 dynein, axonemal, heavy chain 17 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20210506 MGI PMID:31658987 1557331 Tdrd12 tudor domain containing 12 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19897936 1557331 Tdrd12 tudor domain containing 12 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:24067652 1557331 Tdrd12 tudor domain containing 12 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19897936 1557331 Tdrd12 tudor domain containing 12 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:24067652 1557331 Tdrd12 tudor domain containing 12 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19897936 1557331 Tdrd12 tudor domain containing 12 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:24067652 1557331 Tdrd12 tudor domain containing 12 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:24067652 1557331 Tdrd12 tudor domain containing 12 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:24067652 1557331 Tdrd12 tudor domain containing 12 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:24067652 1557331 Tdrd12 tudor domain containing 12 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19897936 1557331 Tdrd12 tudor domain containing 12 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:19897936 1557331 Tdrd12 tudor domain containing 12 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:19897936 1557331 Tdrd12 tudor domain containing 12 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:24067652 1557331 Tdrd12 tudor domain containing 12 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19897936 1557331 Tdrd12 tudor domain containing 12 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:19897936 1557331 Tdrd12 tudor domain containing 12 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:24067652 1557331 Tdrd12 tudor domain containing 12 gene MP:0008261 arrest of male meiosis IEA N RGD:5509061 20141003 MGI 1557332 Hmgb3 high mobility group box 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:15358624 1557332 Hmgb3 high mobility group box 3 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15358624 1557332 Hmgb3 high mobility group box 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12714519 1557332 Hmgb3 high mobility group box 3 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:15358624 1557332 Hmgb3 high mobility group box 3 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:15358624 1557332 Hmgb3 high mobility group box 3 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15358624 1557332 Hmgb3 high mobility group box 3 gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15358624 1557332 Hmgb3 high mobility group box 3 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:15358624 1557332 Hmgb3 high mobility group box 3 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15358624 1557332 Hmgb3 high mobility group box 3 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15358624 1557333 Tdp2 tyrosyl-DNA phosphodiesterase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19598121 1557333 Tdp2 tyrosyl-DNA phosphodiesterase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23505375 1557333 Tdp2 tyrosyl-DNA phosphodiesterase 2 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23505375 1557333 Tdp2 tyrosyl-DNA phosphodiesterase 2 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:23505375 1557333 Tdp2 tyrosyl-DNA phosphodiesterase 2 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:23505375 1557333 Tdp2 tyrosyl-DNA phosphodiesterase 2 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:23505375 1557333 Tdp2 tyrosyl-DNA phosphodiesterase 2 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:23505375 1557333 Tdp2 tyrosyl-DNA phosphodiesterase 2 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:23505375 1557333 Tdp2 tyrosyl-DNA phosphodiesterase 2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:23505375 1557333 Tdp2 tyrosyl-DNA phosphodiesterase 2 gene MP:0005022 abnormal immature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23505375 1557333 Tdp2 tyrosyl-DNA phosphodiesterase 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23505375 1557333 Tdp2 tyrosyl-DNA phosphodiesterase 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23505375 1557333 Tdp2 tyrosyl-DNA phosphodiesterase 2 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:23505375 1557333 Tdp2 tyrosyl-DNA phosphodiesterase 2 gene MP:0011176 abnormal erythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:23505375 1557333 Tdp2 tyrosyl-DNA phosphodiesterase 2 gene MP:0014078 small intestinal villus atrophy IAGP N RGD:5509061 20160414 MGI PMID:23505375 1557334 Usp46 ubiquitin specific peptidase 46 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19465912 1557334 Usp46 ubiquitin specific peptidase 46 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:19465912 1557334 Usp46 ubiquitin specific peptidase 46 gene MP:0002863 improved righting response IAGP N RGD:5509061 20141003 MGI PMID:19465912 1557334 Usp46 ubiquitin specific peptidase 46 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:19465912 1557334 Usp46 ubiquitin specific peptidase 46 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:22720038 1557337 Mrgprb2 MAS-related GPR, member B2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 1557337 Mrgprb2 MAS-related GPR, member B2 gene MP:0000692 small spleen IEA N RGD:5509061 20210826 MGI 1557337 Mrgprb2 MAS-related GPR, member B2 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 1557337 Mrgprb2 MAS-related GPR, member B2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1557337 Mrgprb2 MAS-related GPR, member B2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20160304 MGI PMID:25517090 1557337 Mrgprb2 MAS-related GPR, member B2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1557337 Mrgprb2 MAS-related GPR, member B2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20190502 MGI 1557337 Mrgprb2 MAS-related GPR, member B2 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20210826 MGI 1557337 Mrgprb2 MAS-related GPR, member B2 gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 1557337 Mrgprb2 MAS-related GPR, member B2 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210826 MGI 1557337 Mrgprb2 MAS-related GPR, member B2 gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20160304 MGI PMID:25517090 1557337 Mrgprb2 MAS-related GPR, member B2 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210826 MGI 1557339 Ercc6l2 excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20211118 MGI PMID:32355287 1557339 Ercc6l2 excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20211118 MGI PMID:32355287 1557339 Ercc6l2 excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20211118 MGI PMID:32355287 1557339 Ercc6l2 excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20211118 MGI PMID:32355287 1557339 Ercc6l2 excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20211118 MGI PMID:32355287 1557339 Ercc6l2 excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20211118 MGI PMID:32355287 1557339 Ercc6l2 excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20211118 MGI PMID:32355287 1557339 Ercc6l2 excision repair cross-complementing rodent repair deficiency, complementation group 6 like 2 gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20211118 MGI PMID:32355287 1557340 Arl6ip1 ADP-ribosylation factor-like 6 interacting protein 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1557340 Arl6ip1 ADP-ribosylation factor-like 6 interacting protein 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20170105 MGI 1557340 Arl6ip1 ADP-ribosylation factor-like 6 interacting protein 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20170105 MGI 1557340 Arl6ip1 ADP-ribosylation factor-like 6 interacting protein 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20170105 MGI 1557340 Arl6ip1 ADP-ribosylation factor-like 6 interacting protein 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20170105 MGI 1557342 Ccnb3 cyclin B3 gene MP:0001926 female infertility IAGP N RGD:5509061 20190502 MGI PMID:30723090 1557342 Ccnb3 cyclin B3 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20190502 MGI PMID:30723090 1557342 Ccnb3 cyclin B3 gene MP:0012736 abnormal polar body morphology IAGP N RGD:5509061 20190502 MGI PMID:30723090 1557343 Rnft1 ring finger protein, transmembrane 1 gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20200514 MGI 1557343 Rnft1 ring finger protein, transmembrane 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1557343 Rnft1 ring finger protein, transmembrane 1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 1557344 Cnih3 cornichon family AMPA receptor auxiliary protein 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:23522044 1557344 Cnih3 cornichon family AMPA receptor auxiliary protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23522044 1557344 Cnih3 cornichon family AMPA receptor auxiliary protein 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23522044 1557344 Cnih3 cornichon family AMPA receptor auxiliary protein 3 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23522044 1557345 Tead1 TEA domain family member 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:7958896 1557345 Tead1 TEA domain family member 1 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:7958896 1557345 Tead1 TEA domain family member 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7958896 1557345 Tead1 TEA domain family member 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0000828 abnormal fourth ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:7958896 1557345 Tead1 TEA domain family member 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1557345 Tead1 TEA domain family member 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1557345 Tead1 TEA domain family member 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:7958896 1557345 Tead1 TEA domain family member 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20181227 MGI 1557345 Tead1 TEA domain family member 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141225 MGI 1557345 Tead1 TEA domain family member 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20240523 MGI 1557345 Tead1 TEA domain family member 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:7958896 1557345 Tead1 TEA domain family member 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:7958896 1557345 Tead1 TEA domain family member 1 gene MP:0005543 decreased cornea thickness IEA N RGD:5509061 20210128 MGI 1557345 Tead1 TEA domain family member 1 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0008534 enlarged fourth ventricle IAGP N RGD:5509061 20141003 MGI PMID:7958896 1557345 Tead1 TEA domain family member 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1557345 Tead1 TEA domain family member 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1557345 Tead1 TEA domain family member 1 gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7958896 1557345 Tead1 TEA domain family member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557345 Tead1 TEA domain family member 1 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20210128 MGI 1557345 Tead1 TEA domain family member 1 gene MP:0013217 abnormal posterior definitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18332127 1557345 Tead1 TEA domain family member 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1557345 Tead1 TEA domain family member 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:18332127 1557346 Foxj2 forkhead box J2 gene MP:0001925 male infertility IAGP N RGD:5509061 20210506 MGI PMID:27316861 1557346 Foxj2 forkhead box J2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210506 MGI PMID:27316861 1557346 Foxj2 forkhead box J2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20210506 MGI PMID:27316861 1557346 Foxj2 forkhead box J2 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20210506 MGI PMID:27316861 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000160 kyphosis IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20160707 MGI PMID:20693262 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20160707 MGI PMID:20693262 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20160707 MGI PMID:20696672 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20160707 MGI PMID:20696672 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000745 tremors IAGP N RGD:5509061 20160707 MGI PMID:10655541 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000753 paralysis IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20160707 MGI PMID:19329542 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20160707 MGI PMID:10655541 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20160707 MGI PMID:15703193 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20160707 MGI PMID:18178576 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000947 convulsive seizures IEA N RGD:5509061 20151015 MGI 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001007 abnormal sympathetic system morphology IAGP N RGD:5509061 20160707 MGI PMID:20693262 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20160707 MGI PMID:18065780 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20160707 MGI PMID:15703193 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20160707 MGI PMID:18065780 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20160707 MGI PMID:23390132 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001220 epidermal necrosis IAGP N RGD:5509061 20160707 MGI PMID:23390132 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160707 MGI PMID:15703193 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160707 MGI PMID:23390132 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001263 weight loss IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001263 weight loss IAGP N RGD:5509061 20160707 MGI PMID:20693262 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160707 MGI PMID:20693262 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160707 MGI PMID:23390132 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210128 MGI 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001378 abnormal ejaculation IAGP N RGD:5509061 20230216 MGI PMID:32865662 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160707 MGI PMID:23390132 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160707 MGI PMID:15703193 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20160707 MGI PMID:10655541 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001443 poor grooming IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:9920659 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001513 limb grasping IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20160707 MGI PMID:15703193 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20160707 MGI PMID:23390132 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20160707 MGI PMID:15703193 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001525 impaired balance IAGP N RGD:5509061 20160707 MGI PMID:15703193 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20230216 MGI PMID:32865662 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20160707 MGI PMID:10655541 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0001956 hypopnea IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:9920659 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20160707 MGI PMID:23390132 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002083 premature death IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002083 premature death IAGP N RGD:5509061 20160707 MGI PMID:18178576 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002083 premature death IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002083 premature death IAGP N RGD:5509061 20160707 MGI PMID:23390132 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20160707 MGI PMID:20696672 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20230216 MGI PMID:32865662 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002738 hyperresponsive to tactile stimuli IEA N RGD:5509061 20151015 MGI 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20160707 MGI PMID:20693262 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:9920659 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:18716219 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18716219 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20160707 MGI PMID:19329542 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0003466 decreased single cell response threshold IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20160707 MGI PMID:20696672 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20160707 MGI PMID:20693262 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0003928 increased heart rate variability IAGP N RGD:5509061 20160707 MGI PMID:20693262 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0004243 abnormal motor nerve collateral sprouting IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20160707 MGI PMID:10655541 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0005202 lethargy IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20160707 MGI PMID:20693262 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20160707 MGI PMID:20696672 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20160707 MGI PMID:12515823 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20160707 MGI PMID:20696672 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20160707 MGI PMID:23390132 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0006404 abnormal lumbar dorsal root ganglion morphology IAGP N RGD:5509061 20160707 MGI PMID:18178576 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:18716219 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20160707 MGI PMID:18178576 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20160707 MGI PMID:23390132 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20160707 MGI PMID:18065780 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20160707 MGI PMID:15703193 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18716219 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0009856 failure of ejaculation IAGP N RGD:5509061 20230216 MGI PMID:32865662 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160707 MGI PMID:23390132 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20160707 MGI PMID:20693262 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20160707 MGI PMID:20696672 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20160707 MGI PMID:20696672 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20160707 MGI PMID:20696672 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20160707 MGI PMID:23390132 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160707 MGI PMID:10655541 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160707 MGI PMID:15703193 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160707 MGI PMID:18178576 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160707 MGI PMID:19329542 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160707 MGI PMID:20693262 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160707 MGI PMID:20826664 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160707 MGI PMID:22423102 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20160707 MGI PMID:10655541 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20160707 MGI PMID:20696672 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20180308 MGI PMID:29371219 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0013178 tail necrosis IAGP N RGD:5509061 20160707 MGI PMID:18178576 1557347 Grm7 glutamate receptor, metabotropic 7 gene MP:0031628 abnormal intromission IAGP N RGD:5509061 20240704 MGI PMID:32865662 1557349 Hmx3 H6 homeobox 3 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:9389661 1557349 Hmx3 H6 homeobox 3 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:9435283 1557349 Hmx3 H6 homeobox 3 gene MP:0000041 absent endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:9389661 1557349 Hmx3 H6 homeobox 3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:9435283 1557349 Hmx3 H6 homeobox 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:9389661 1557349 Hmx3 H6 homeobox 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:9435283 1557349 Hmx3 H6 homeobox 3 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:9435283 1557349 Hmx3 H6 homeobox 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9389661 1557349 Hmx3 H6 homeobox 3 gene MP:0001752 abnormal hypothalamus secretion IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9435283 1557349 Hmx3 H6 homeobox 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9389661 1557349 Hmx3 H6 homeobox 3 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:12142028 1557349 Hmx3 H6 homeobox 3 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:9389661 1557349 Hmx3 H6 homeobox 3 gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:9389661 1557349 Hmx3 H6 homeobox 3 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:9389661 1557349 Hmx3 H6 homeobox 3 gene MP:0003164 decreased posterior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:9389661 1557349 Hmx3 H6 homeobox 3 gene MP:0003166 decreased superior semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:9389661 1557349 Hmx3 H6 homeobox 3 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:9435283 1557349 Hmx3 H6 homeobox 3 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:9435283 1557349 Hmx3 H6 homeobox 3 gene MP:0004314 absent inner ear vestibule IAGP N RGD:5509061 20141003 MGI PMID:9389661 1557349 Hmx3 H6 homeobox 3 gene MP:0004328 decreased vestibular hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0004329 vestibular saccular degeneration IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0004331 vestibular saccular macula degeneration IAGP N RGD:5509061 20141003 MGI PMID:9435283 1557349 Hmx3 H6 homeobox 3 gene MP:0004332 utricular degeneration IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0004334 utricular macular degeneration IAGP N RGD:5509061 20141003 MGI PMID:9435283 1557349 Hmx3 H6 homeobox 3 gene MP:0004425 abnormal otolith organ morphology IAGP N RGD:5509061 20141003 MGI PMID:9435283 1557349 Hmx3 H6 homeobox 3 gene MP:0004427 abnormal vestibular labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:9435283 1557349 Hmx3 H6 homeobox 3 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:9435283 1557349 Hmx3 H6 homeobox 3 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9435283 1557349 Hmx3 H6 homeobox 3 gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15363417 1557349 Hmx3 H6 homeobox 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9435283 1557350 Pax9 paired box 9 gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20141003 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0000094 absent alveolar process IAGP N RGD:5509061 20141003 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0000094 absent alveolar process IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0000111 cleft palate IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:21420399 1557350 Pax9 paired box 9 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:21420399 1557350 Pax9 paired box 9 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0000128 growth retardation of molars IAGP N RGD:5509061 20141003 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:21420399 1557350 Pax9 paired box 9 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21420399 1557350 Pax9 paired box 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0002256 abnormal laryngeal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0002367 abnormal thymus lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20141003 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0003404 absent enamel IAGP N RGD:5509061 20141003 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0003931 absent molars IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0004537 abnormal palatine bone horizontal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20141003 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0004552 fused tracheal cartilage rings IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:21420399 1557350 Pax9 paired box 9 gene MP:0004791 absent lower incisors IAGP N RGD:5509061 20141003 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20141003 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20141003 MGI PMID:21420399 1557350 Pax9 paired box 9 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0004914 absent ultimobranchial body IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0004915 abnormal Reichert's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0004916 absent Reichert cartilage IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0005382 craniofacial phenotype IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:21420399 1557350 Pax9 paired box 9 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0006400 decreased molar number IAGP N RGD:5509061 20141003 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:21420399 1557350 Pax9 paired box 9 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0009843 decreased neural crest cell number IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:21420399 1557350 Pax9 paired box 9 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:21420399 1557350 Pax9 paired box 9 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0009913 abnormal hyoid bone greater horn morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0010355 abnormal first pharyngeal arch artery morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0010356 abnormal second pharyngeal arch artery morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21420399 1557350 Pax9 paired box 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0021207 abnormal autopod muscle morphology IAGP N RGD:5509061 20221201 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0030084 tympanic ring hypoplasia IAGP N RGD:5509061 20241031 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:21420399 1557350 Pax9 paired box 9 gene MP:0030335 absent third pharyngeal arch artery IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0030336 third pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0030340 absent fourth pharyngeal arch artery IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0030341 fourth pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0030459 abnormal tooth attrition IAGP N RGD:5509061 20180125 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0030542 abnormal dentin development IAGP N RGD:5509061 20180215 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0030608 decreased tooth number IAGP N RGD:5509061 20180726 MGI PMID:16236760 1557350 Pax9 paired box 9 gene MP:0030608 decreased tooth number IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:17610273 1557350 Pax9 paired box 9 gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:9732271 1557350 Pax9 paired box 9 gene MP:0030870 abnormal superior horn of thyroid cartilage morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0030871 abnormal inferior horn of thyroid cartilage morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 1557350 Pax9 paired box 9 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:21420399 1557350 Pax9 paired box 9 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:9732271 1557351 Porcn porcupine O-acyltransferase gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0000111 cleft palate IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0000564 syndactyly IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0000592 short tail IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0001215 skin hypoplasia IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0001297 microphthalmia IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:23760955 1557351 Porcn porcupine O-acyltransferase gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:23760955 1557351 Porcn porcupine O-acyltransferase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23760955 1557351 Porcn porcupine O-acyltransferase gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:23760955 1557351 Porcn porcupine O-acyltransferase gene MP:0001725 abnormal umbilical cord morphology IAGP N RGD:5509061 20141003 MGI PMID:23760955 1557351 Porcn porcupine O-acyltransferase gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:23760955 1557351 Porcn porcupine O-acyltransferase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0002085 abnormal embryonic tissue morphology IEA N RGD:5509061 20111116 MGI 1557351 Porcn porcupine O-acyltransferase gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:23760955 1557351 Porcn porcupine O-acyltransferase gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23760955 1557351 Porcn porcupine O-acyltransferase gene MP:0002213 true hermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0003051 curly tail IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0004323 sternum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0004360 absent ulna IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:23760955 1557351 Porcn porcupine O-acyltransferase gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0005262 coloboma IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0009085 abnormal uterine horn morphology IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0009593 absent chorion IAGP N RGD:5509061 20141003 MGI PMID:23760955 1557351 Porcn porcupine O-acyltransferase gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23760955 1557351 Porcn porcupine O-acyltransferase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23760955 1557351 Porcn porcupine O-acyltransferase gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0011156 abnormal hypodermis fat layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22412863 1557351 Porcn porcupine O-acyltransferase gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0013283 failure of ventral body wall closure IAGP N RGD:5509061 20191114 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:25451153 1557351 Porcn porcupine O-acyltransferase gene MP:0014291 decreased autopod size IAGP N RGD:5509061 20230824 MGI PMID:21768372 1557351 Porcn porcupine O-acyltransferase gene MP:0031445 midline cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:25451153 1557352 Stk31 serine threonine kinase 31 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23929668 1557354 Ttyh2 tweety family member 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20220609 MGI PMID:29527922 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20220609 MGI PMID:29527922 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20220609 MGI PMID:29527922 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0000160 kyphosis IAGP N RGD:5509061 20220609 MGI PMID:29527922 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:24240089 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220609 MGI PMID:29527922 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20220609 MGI PMID:29527922 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20220609 MGI PMID:29527922 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20220609 MGI PMID:29527922 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20220609 MGI PMID:29527922 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20211021 MGI 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20220609 MGI PMID:29527922 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:24240089 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20141003 MGI PMID:24240089 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20220609 MGI PMID:29527922 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20220609 MGI PMID:29527922 1557355 Idh2 isocitrate dehydrogenase 2 (NADP+), mitochondrial gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20220609 MGI PMID:29527922 1557356 Rad51b RAD51 paralog B gene MP:0006206 embryonic lethality between somite formation and embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10567591 1557356 Rad51b RAD51 paralog B gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10567591 1557359 Brcc3 BRCA1/BRCA2-containing complex, subunit 3 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20211021 MGI 1557361 Vps13c vacuolar protein sorting 13C gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230119 MGI 1557361 Vps13c vacuolar protein sorting 13C gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20170831 MGI PMID:27329800 1557361 Vps13c vacuolar protein sorting 13C gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230119 MGI 1557361 Vps13c vacuolar protein sorting 13C gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 1557361 Vps13c vacuolar protein sorting 13C gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20170831 MGI PMID:27329800 1557361 Vps13c vacuolar protein sorting 13C gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230119 MGI 1557361 Vps13c vacuolar protein sorting 13C gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20170831 MGI PMID:27329800 1557361 Vps13c vacuolar protein sorting 13C gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230119 MGI 1557361 Vps13c vacuolar protein sorting 13C gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20210128 MGI 1557361 Vps13c vacuolar protein sorting 13C gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1557361 Vps13c vacuolar protein sorting 13C gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20230119 MGI 1557361 Vps13c vacuolar protein sorting 13C gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20170105 MGI 1557361 Vps13c vacuolar protein sorting 13C gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230119 MGI 1557362 Zfp445 zinc finger protein 445 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210826 MGI 1557362 Zfp445 zinc finger protein 445 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20181227 MGI 1557362 Zfp445 zinc finger protein 445 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1557362 Zfp445 zinc finger protein 445 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1557362 Zfp445 zinc finger protein 445 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1557362 Zfp445 zinc finger protein 445 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557362 Zfp445 zinc finger protein 445 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1557363 Msh3 mutS homolog 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1557363 Msh3 mutS homolog 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1557363 Msh3 mutS homolog 3 gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1557363 Msh3 mutS homolog 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1557363 Msh3 mutS homolog 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10706084 1557363 Msh3 mutS homolog 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1557363 Msh3 mutS homolog 3 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1557363 Msh3 mutS homolog 3 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10706084 1557363 Msh3 mutS homolog 3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1557363 Msh3 mutS homolog 3 gene MP:0009797 abnormal mismatch repair IAGP N RGD:5509061 20141003 MGI PMID:10706084 1557363 Msh3 mutS homolog 3 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10545954 1557363 Msh3 mutS homolog 3 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10706084 1557363 Msh3 mutS homolog 3 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10545954 1557363 Msh3 mutS homolog 3 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10545954 1557363 Msh3 mutS homolog 3 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10706084 1557363 Msh3 mutS homolog 3 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:10545954 1557364 Stard13 StAR related lipid transfer domain containing 13 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557364 Stard13 StAR related lipid transfer domain containing 13 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557364 Stard13 StAR related lipid transfer domain containing 13 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19668331 1557364 Stard13 StAR related lipid transfer domain containing 13 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19668331 1557364 Stard13 StAR related lipid transfer domain containing 13 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23175628 1557364 Stard13 StAR related lipid transfer domain containing 13 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557364 Stard13 StAR related lipid transfer domain containing 13 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557364 Stard13 StAR related lipid transfer domain containing 13 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20208559 1557364 Stard13 StAR related lipid transfer domain containing 13 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:23175628 1557364 Stard13 StAR related lipid transfer domain containing 13 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23175628 1557364 Stard13 StAR related lipid transfer domain containing 13 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20208559 1557364 Stard13 StAR related lipid transfer domain containing 13 gene MP:0009111 pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23175628 1557364 Stard13 StAR related lipid transfer domain containing 13 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19668331 1557364 Stard13 StAR related lipid transfer domain containing 13 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:20208559 1557367 Socs5 suppressor of cytokine signaling 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15199163 1557367 Socs5 suppressor of cytokine signaling 5 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:17611223 1557369 Atp23 ATP23 metallopeptidase and ATP synthase assembly factor homolog gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20220714 MGI PMID:35682694 1557369 Atp23 ATP23 metallopeptidase and ATP synthase assembly factor homolog gene MP:0001177 atelectasis IAGP N RGD:5509061 20220714 MGI PMID:35682694 1557369 Atp23 ATP23 metallopeptidase and ATP synthase assembly factor homolog gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20220714 MGI PMID:35682694 1557369 Atp23 ATP23 metallopeptidase and ATP synthase assembly factor homolog gene MP:0003641 small lung IAGP N RGD:5509061 20220714 MGI PMID:35682694 1557369 Atp23 ATP23 metallopeptidase and ATP synthase assembly factor homolog gene MP:0003717 pallor IAGP N RGD:5509061 20220714 MGI PMID:35682694 1557369 Atp23 ATP23 metallopeptidase and ATP synthase assembly factor homolog gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20220714 MGI PMID:35682694 1557369 Atp23 ATP23 metallopeptidase and ATP synthase assembly factor homolog gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20220714 MGI PMID:35682694 1557369 Atp23 ATP23 metallopeptidase and ATP synthase assembly factor homolog gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20220714 MGI PMID:35682694 1557369 Atp23 ATP23 metallopeptidase and ATP synthase assembly factor homolog gene MP:0010887 pale lung IAGP N RGD:5509061 20220714 MGI PMID:35682694 1557369 Atp23 ATP23 metallopeptidase and ATP synthase assembly factor homolog gene MP:0010890 decreased alveolar lamellar body number IAGP N RGD:5509061 20220714 MGI PMID:35682694 1557369 Atp23 ATP23 metallopeptidase and ATP synthase assembly factor homolog gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20220714 MGI PMID:35682694 1557369 Atp23 ATP23 metallopeptidase and ATP synthase assembly factor homolog gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20220714 MGI PMID:35682694 1557371 Sash1 SAM and SH3 domain containing 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1557371 Sash1 SAM and SH3 domain containing 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1557371 Sash1 SAM and SH3 domain containing 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1557371 Sash1 SAM and SH3 domain containing 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1557371 Sash1 SAM and SH3 domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557374 Ino80b INO80 complex subunit B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1557374 Ino80b INO80 complex subunit B gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20231207 MGI 1557377 Rnf114 ring finger protein 114 gene MP:0001926 female infertility IAGP N RGD:5509061 20210930 MGI PMID:34104941 1557377 Rnf114 ring finger protein 114 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1557377 Rnf114 ring finger protein 114 gene MP:0003718 maternal effect IAGP N RGD:5509061 20210930 MGI PMID:34104941 1557377 Rnf114 ring finger protein 114 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20210930 MGI PMID:34104941 1557378 Srsf11 serine and arginine-rich splicing factor 11 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20211021 MGI 1557378 Srsf11 serine and arginine-rich splicing factor 11 gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20211021 MGI 1557378 Srsf11 serine and arginine-rich splicing factor 11 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1557378 Srsf11 serine and arginine-rich splicing factor 11 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557378 Srsf11 serine and arginine-rich splicing factor 11 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201224 MGI PMID:30582011 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230601 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230601 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0002083 premature death IAGP N RGD:5509061 20201224 MGI PMID:30582011 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20191212 MGI PMID:29263159 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20201224 MGI PMID:30582011 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0002871 albuminuria IAGP N RGD:5509061 20191212 MGI PMID:29263159 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0002871 albuminuria IAGP N RGD:5509061 20201224 MGI PMID:30582011 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20201224 MGI PMID:30582011 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0003236 abnormal lens capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:23707242 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005161 hematuria IAGP N RGD:5509061 20201224 MGI PMID:30582011 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:23707242 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20191212 MGI PMID:29263159 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20201224 MGI PMID:30582011 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20201224 MGI PMID:30582011 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20201224 MGI PMID:30582011 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20201224 MGI PMID:30582011 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20201224 MGI PMID:30582011 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20201224 MGI PMID:30582011 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20201224 MGI PMID:30582011 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20201224 MGI PMID:30582011 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20201224 MGI PMID:30582011 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0011483 renal glomerular synechia IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0011509 dilated glomerular capillary IAGP N RGD:5509061 20141003 MGI PMID:15153557 1557379 Col4a5 collagen, type IV, alpha 5 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20210128 MGI 1557380 Zpbp zona pellucida binding protein gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17664285 1557380 Zpbp zona pellucida binding protein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17664285 1557380 Zpbp zona pellucida binding protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17664285 1557380 Zpbp zona pellucida binding protein gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17664285 1557380 Zpbp zona pellucida binding protein gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17664285 1557380 Zpbp zona pellucida binding protein gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17664285 1557380 Zpbp zona pellucida binding protein gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17664285 1557380 Zpbp zona pellucida binding protein gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17664285 1557380 Zpbp zona pellucida binding protein gene MP:0008839 absent acrosome IAGP N RGD:5509061 20141003 MGI PMID:17664285 1557380 Zpbp zona pellucida binding protein gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17664285 1557380 Zpbp zona pellucida binding protein gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:17664285 1557380 Zpbp zona pellucida binding protein gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17664285 1557380 Zpbp zona pellucida binding protein gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:17664285 1557380 Zpbp zona pellucida binding protein gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:17664285 1557381 Map3k9 mitogen-activated protein kinase kinase kinase 9 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1557381 Map3k9 mitogen-activated protein kinase kinase kinase 9 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220811 MGI 1557381 Map3k9 mitogen-activated protein kinase kinase kinase 9 gene MP:0001148 enlarged testis IEA N RGD:5509061 20220811 MGI 1557381 Map3k9 mitogen-activated protein kinase kinase kinase 9 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1557381 Map3k9 mitogen-activated protein kinase kinase kinase 9 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1557381 Map3k9 mitogen-activated protein kinase kinase kinase 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18414056 1557381 Map3k9 mitogen-activated protein kinase kinase kinase 9 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1557381 Map3k9 mitogen-activated protein kinase kinase kinase 9 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210520 MGI 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000088 short mandible IAGP N RGD:5509061 20180201 MGI PMID:24895408 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20180201 MGI PMID:19307312 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:21768372 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:24895408 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:24168030 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20180201 MGI PMID:24043815 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20180201 MGI PMID:19837032 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20180201 MGI PMID:23303524 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20180201 MGI PMID:26494787 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20180201 MGI PMID:12842913 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20180201 MGI PMID:25953344 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20180201 MGI PMID:12842913 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20180201 MGI PMID:20040491 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20180201 MGI PMID:23303524 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20180201 MGI PMID:26494787 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20180201 MGI PMID:24043815 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20180201 MGI PMID:25953344 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20180201 MGI PMID:12842913 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20180201 MGI PMID:26494787 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20180201 MGI PMID:26494787 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20180201 MGI PMID:21693517 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20180201 MGI PMID:26921005 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20180201 MGI PMID:25190059 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000433 microcephaly IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000445 short snout IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:24895408 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000536 hydroureter IAGP N RGD:5509061 20180201 MGI PMID:19060336 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000547 short limbs IAGP N RGD:5509061 20180201 MGI PMID:19307312 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:16611729 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20180201 MGI PMID:16611729 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000564 syndactyly IAGP N RGD:5509061 20180201 MGI PMID:19307312 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000566 synostosis IAGP N RGD:5509061 20180201 MGI PMID:19307312 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20180201 MGI PMID:21768372 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000592 short tail IAGP N RGD:5509061 20180201 MGI PMID:21768372 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:21768366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:18550708 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000601 small liver IAGP N RGD:5509061 20180201 MGI PMID:21768366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000690 absent spleen IAGP N RGD:5509061 20180201 MGI PMID:19307312 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20210114 MGI PMID:32702291 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000828 abnormal fourth ventricle morphology IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20180201 MGI PMID:18509025 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20180201 MGI PMID:21983115 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20180201 MGI PMID:17619227 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20180201 MGI PMID:21983115 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20180201 MGI PMID:21983115 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20180201 MGI PMID:21983115 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20180201 MGI PMID:21983115 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20180201 MGI PMID:20573697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20180201 MGI PMID:21768366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20180201 MGI PMID:20573697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20180201 MGI PMID:24043815 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20180201 MGI PMID:25809849 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20180201 MGI PMID:22110054 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000932 absent notochord IAGP N RGD:5509061 20240627 MGI PMID:22669107 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20180201 MGI PMID:15215210 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20180201 MGI PMID:18367557 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20180201 MGI PMID:19307312 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001177 atelectasis IAGP N RGD:5509061 20180201 MGI PMID:18367557 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20180201 MGI PMID:18367557 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20180201 MGI PMID:25652406 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20180201 MGI PMID:21768372 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20180201 MGI PMID:26921005 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:17619227 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:18509025 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:26232697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20180201 MGI PMID:26232697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:18509025 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:21768372 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:25652406 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230323 MGI PMID:34767447 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20180201 MGI PMID:20048158 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20180201 MGI PMID:17619227 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001296 macrophthalmia IAGP N RGD:5509061 20180201 MGI PMID:20048158 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20180201 MGI PMID:18509025 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001394 circling IAGP N RGD:5509061 20180201 MGI PMID:17765677 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180201 MGI PMID:18509025 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180201 MGI PMID:21983115 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001407 short stride length IAGP N RGD:5509061 20180201 MGI PMID:21983115 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001410 head bobbing IAGP N RGD:5509061 20180201 MGI PMID:17765677 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20180201 MGI PMID:22763239 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001513 limb grasping IAGP N RGD:5509061 20180201 MGI PMID:21983115 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20180201 MGI PMID:17619227 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20180201 MGI PMID:18367557 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20180201 MGI PMID:18550708 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20180201 MGI PMID:19023080 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20180201 MGI PMID:24043815 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20180201 MGI PMID:21693517 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20180201 MGI PMID:19279185 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20180201 MGI PMID:21094155 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20180201 MGI PMID:21693517 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20180201 MGI PMID:15302604 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20180201 MGI PMID:22991437 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20180201 MGI PMID:21693517 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20180201 MGI PMID:21768372 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20180329 MGI PMID:29203676 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20240627 MGI PMID:22669107 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20180201 MGI PMID:15302604 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20180201 MGI PMID:18171685 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20180201 MGI PMID:18171685 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20180201 MGI PMID:20573697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20180201 MGI PMID:26494787 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20240627 MGI PMID:22669107 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20180201 MGI PMID:23303524 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20240627 MGI PMID:22669107 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20180201 MGI PMID:19830823 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20180201 MGI PMID:22991437 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180201 MGI PMID:18550708 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180201 MGI PMID:20573697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180201 MGI PMID:20978237 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180201 MGI PMID:21693517 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180201 MGI PMID:26921005 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200430 MGI PMID:31950080 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20240627 MGI PMID:22669107 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20180201 MGI PMID:15215210 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20180201 MGI PMID:20040491 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20180201 MGI PMID:19464366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20180201 MGI PMID:20978237 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20180201 MGI PMID:19464366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20180201 MGI PMID:18550708 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20180201 MGI PMID:20978237 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20180201 MGI PMID:23142660 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20180201 MGI PMID:15215210 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20180201 MGI PMID:17060609 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20180201 MGI PMID:20978237 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20180201 MGI PMID:22110054 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180201 MGI PMID:21664579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180201 MGI PMID:25652406 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001785 edema IAGP N RGD:5509061 20180201 MGI PMID:24895408 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20180201 MGI PMID:12842913 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20180201 MGI PMID:19279185 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20180201 MGI PMID:19023080 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20180201 MGI PMID:22516201 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20180201 MGI PMID:25652406 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20180201 MGI PMID:18171685 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20180201 MGI PMID:24043815 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:26232697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20180201 MGI PMID:15302604 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20180201 MGI PMID:21693517 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20180201 MGI PMID:22516201 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20180201 MGI PMID:22991437 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20180201 MGI PMID:23142660 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20180201 MGI PMID:26921005 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20240627 MGI PMID:22669107 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20180201 MGI PMID:16611729 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20180201 MGI PMID:21768372 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20180201 MGI PMID:19307312 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20180201 MGI PMID:22516201 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20180201 MGI PMID:19060336 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20180201 MGI PMID:23303524 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200430 MGI PMID:31950080 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:19219045 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:19279185 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:21664579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:22453236 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190207 MGI PMID:28708136 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002174 abnormal gastrulation movements IAGP N RGD:5509061 20240627 MGI PMID:22669107 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002183 gliosis IAGP N RGD:5509061 20180201 MGI PMID:26232697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002188 small heart IAGP N RGD:5509061 20230323 MGI PMID:34767447 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20240627 MGI PMID:22669107 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20180201 MGI PMID:18171685 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20180201 MGI PMID:19830823 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20180201 MGI PMID:21693517 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20180201 MGI PMID:18550708 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20180201 MGI PMID:26219237 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20180201 MGI PMID:17765677 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:19008446 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20180301 MGI PMID:29097735 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25953344 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20180201 MGI PMID:20048158 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20180201 MGI PMID:20048158 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20180201 MGI PMID:22763239 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20180201 MGI PMID:23217742 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20180201 MGI PMID:21664579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20180201 MGI PMID:23102580 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003052 omphalocele IAGP N RGD:5509061 20180201 MGI PMID:21768372 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20180201 MGI PMID:21768366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20180201 MGI PMID:25809849 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20180531 MGI PMID:28337978 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003116 rickets IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20180201 MGI PMID:22110054 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20180201 MGI PMID:18367557 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003169 abnormal scala media morphology IAGP N RGD:5509061 20180201 MGI PMID:17765677 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20180201 MGI PMID:26232697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20180201 MGI PMID:22110054 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20180201 MGI PMID:23142660 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20180201 MGI PMID:20978237 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20180201 MGI PMID:26232697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003381 vitreal fibroplasia IAGP N RGD:5509061 20180201 MGI PMID:20048158 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20180201 MGI PMID:19307312 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20180201 MGI PMID:21693517 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:21768366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003613 abnormal kidney medulla development IAGP N RGD:5509061 20180201 MGI PMID:19060336 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:19008446 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003641 small lung IAGP N RGD:5509061 20180201 MGI PMID:18367557 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20180201 MGI PMID:26232697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20180201 MGI PMID:21983115 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20180201 MGI PMID:21768372 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20180201 MGI PMID:25190059 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003717 pallor IAGP N RGD:5509061 20180201 MGI PMID:19279185 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003717 pallor IAGP N RGD:5509061 20180201 MGI PMID:20978237 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003717 pallor IAGP N RGD:5509061 20180201 MGI PMID:24895408 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20180201 MGI PMID:21693517 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20181129 MGI PMID:27505251 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003815 hairless IAGP N RGD:5509061 20180201 MGI PMID:21768372 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20180201 MGI PMID:26494787 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20180201 MGI PMID:18171685 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20180201 MGI PMID:19830823 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20180201 MGI PMID:21768366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20180201 MGI PMID:26921005 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180201 MGI PMID:19464366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180201 MGI PMID:19837032 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180201 MGI PMID:24043815 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180201 MGI PMID:26494787 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20180201 MGI PMID:20573697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20180201 MGI PMID:21693517 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20180201 MGI PMID:26494787 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20180201 MGI PMID:21768372 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20180201 MGI PMID:22190642 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20180201 MGI PMID:21693517 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20180201 MGI PMID:26494787 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20180329 MGI PMID:29203676 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20240620 MGI PMID:38453366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20180201 MGI PMID:24895408 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20180201 MGI PMID:20040491 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20180201 MGI PMID:20040491 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20180201 MGI PMID:23217742 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004323 sternum hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:21768372 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004360 absent ulna IAGP N RGD:5509061 20180201 MGI PMID:21768372 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20180201 MGI PMID:24895408 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004559 small allantois IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004575 small limb buds IAGP N RGD:5509061 20180201 MGI PMID:19307312 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20180201 MGI PMID:19307312 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20180201 MGI PMID:22833677 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0004887 decreased endolymph production IAGP N RGD:5509061 20180201 MGI PMID:17765677 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005034 abnormal anus morphology IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20180201 MGI PMID:26232697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20180201 MGI PMID:16611729 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20180201 MGI PMID:25809849 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005163 cyclopia IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005167 abnormal blood-brain barrier function IAGP N RGD:5509061 20180201 MGI PMID:19023080 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:24168030 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20180201 MGI PMID:12842913 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20180201 MGI PMID:15215210 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20240627 MGI PMID:22669107 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20180201 MGI PMID:19307312 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20180201 MGI PMID:21664579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005352 small cranium IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005352 small cranium IAGP N RGD:5509061 20180201 MGI PMID:24895408 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20180201 MGI PMID:25652406 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20180201 MGI PMID:20048158 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20180201 MGI PMID:17639082 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20180201 MGI PMID:18367557 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20180201 MGI PMID:26921005 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20180201 MGI PMID:19023080 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0006063 abnormal inferior vena cava morphology IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0006063 abnormal inferior vena cava morphology IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20180201 MGI PMID:20048158 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20180201 MGI PMID:15215210 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20180301 MGI PMID:29097735 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20180201 MGI PMID:19644017 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0006290 proboscis IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20180201 MGI PMID:17765677 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20180201 MGI PMID:18550708 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20181129 MGI PMID:27505251 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20180201 MGI PMID:22763239 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008308 small scala media IAGP N RGD:5509061 20180201 MGI PMID:17765677 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008393 absent primordial germ cells IAGP N RGD:5509061 20180201 MGI PMID:15215210 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20180201 MGI PMID:17765677 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20180201 MGI PMID:20048158 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20180201 MGI PMID:20048158 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20180201 MGI PMID:20048158 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20180201 MGI PMID:21983115 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20180201 MGI PMID:19279185 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20180201 MGI PMID:20079728 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20180201 MGI PMID:23142660 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20181129 MGI PMID:27505251 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008903 abnormal mesenteric fat pad morphology IAGP N RGD:5509061 20180201 MGI PMID:21664579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008918 microgliosis IAGP N RGD:5509061 20180201 MGI PMID:26232697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008926 abnormal anterior definitive endoderm morphology IAGP N RGD:5509061 20180201 MGI PMID:12842913 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20180201 MGI PMID:22763239 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20180201 MGI PMID:18550708 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009022 abnormal brain meninges morphology IAGP N RGD:5509061 20180201 MGI PMID:21983115 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009026 abnormal brain pia mater morphology IAGP N RGD:5509061 20180201 MGI PMID:21983115 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009130 increased white fat cell number IAGP N RGD:5509061 20180201 MGI PMID:21664579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20180201 MGI PMID:20573697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009323 abnormal spleen development IAGP N RGD:5509061 20180201 MGI PMID:19307312 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20240627 MGI PMID:22669107 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009445 osteomalacia IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20180201 MGI PMID:23217742 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009573 abnormal right lung middle lobe morphology IAGP N RGD:5509061 20180201 MGI PMID:18367557 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20180201 MGI PMID:20048158 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20180201 MGI PMID:23217742 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009695 abnormal spinal cord ventral commissure morphology IAGP N RGD:5509061 20180201 MGI PMID:23217742 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20210422 MGI PMID:26851218 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20180201 MGI PMID:17619227 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20180201 MGI PMID:16611729 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20211021 MGI PMID:32280065 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20180201 MGI PMID:21693517 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:19008446 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20180201 MGI PMID:19837032 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20180201 MGI PMID:21664579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009869 abnormal descending aorta morphology IAGP N RGD:5509061 20180201 MGI PMID:19837032 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20180201 MGI PMID:24895408 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20180201 MGI PMID:15576405 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20180201 MGI PMID:22763239 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20180201 MGI PMID:21768366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20180201 MGI PMID:20048158 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20180201 MGI PMID:20048158 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20180201 MGI PMID:22110054 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010126 abnormal distal visceral endoderm morphology IAGP N RGD:5509061 20180201 MGI PMID:15302604 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010235 abnormal retina inner limiting membrane morphology IAGP N RGD:5509061 20180201 MGI PMID:20048158 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010387 abnormal Bergmann glial cell morphology IAGP N RGD:5509061 20180201 MGI PMID:21983115 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:21768366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:25953344 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010437 absent coronary sinus IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20240627 MGI PMID:22669107 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010807 abnormal stomach position or orientation IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010853 abnormal lung position or orientation IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20180201 MGI PMID:21664579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:17619227 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:21664579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:21768366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:25190059 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:25809849 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:21768366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210422 MGI PMID:26851218 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:18367557 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:24895408 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20210422 MGI PMID:26851218 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:15576405 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:16611729 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:21768372 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:19837032 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:20689803 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:22991437 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:26553930 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200430 MGI PMID:31950080 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240620 MGI PMID:38453366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:18974357 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:25480920 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:26290337 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:26921005 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180322 MGI PMID:29415061 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20221229 MGI PMID:29967292 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:17060609 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:16467350 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20210114 MGI PMID:32702291 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:15215210 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:18550708 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:19023080 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:19279185 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:20040491 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:20978237 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:25953344 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20230323 MGI PMID:34767447 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:19307312 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:21768366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:21768372 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:23028370 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:23824717 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:26292834 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20240620 MGI PMID:38453366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:19464366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:19690388 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:19837032 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:20573697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20201015 MGI PMID:32658897 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:18440989 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:23184148 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:25809849 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20230323 MGI PMID:34767447 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011144 thin lung-associated mesenchyme IAGP N RGD:5509061 20180201 MGI PMID:18367557 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011148 decreased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20180201 MGI PMID:18367557 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011156 abnormal hypodermis fat layer morphology IAGP N RGD:5509061 20180201 MGI PMID:21664579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011169 abnormal white fat cell differentation IAGP N RGD:5509061 20180201 MGI PMID:21664579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20180201 MGI PMID:18171685 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20240627 MGI PMID:22669107 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20180201 MGI PMID:20978237 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011257 abnormal head fold morphology IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011257 abnormal head fold morphology IAGP N RGD:5509061 20180329 MGI PMID:29203676 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011345 truncated loop of Henle IAGP N RGD:5509061 20180201 MGI PMID:19060336 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20180201 MGI PMID:19060336 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011438 absent kidney medulla IAGP N RGD:5509061 20180201 MGI PMID:19060336 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011439 abnormal kidney cell proliferation IAGP N RGD:5509061 20180201 MGI PMID:19060336 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20180201 MGI PMID:19060336 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011504 abnormal limb long bone morphology IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20180201 MGI PMID:20978237 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20240620 MGI PMID:38453366 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011733 fused somites IAGP N RGD:5509061 20180201 MGI PMID:12842913 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011733 fused somites IAGP N RGD:5509061 20180201 MGI PMID:15215210 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011843 abnormal kidney collecting duct epithelium morphology IAGP N RGD:5509061 20180201 MGI PMID:19060336 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20180201 MGI PMID:17765677 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012083 absent foregut IAGP N RGD:5509061 20180201 MGI PMID:12842913 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012083 absent foregut IAGP N RGD:5509061 20180201 MGI PMID:15215210 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012084 truncated foregut IAGP N RGD:5509061 20180201 MGI PMID:12842913 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012086 absent hindgut IAGP N RGD:5509061 20180201 MGI PMID:15215210 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20180201 MGI PMID:12842913 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012091 increased midbrain size IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20180201 MGI PMID:12842913 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012139 increased forebrain size IAGP N RGD:5509061 20180201 MGI PMID:17468181 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20180201 MGI PMID:12842913 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20180201 MGI PMID:18171685 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20180201 MGI PMID:22110054 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20180329 MGI PMID:29203676 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012175 flat face IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012671 retina spots IAGP N RGD:5509061 20180201 MGI PMID:20048158 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20180201 MGI PMID:20040491 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20180201 MGI PMID:20573697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20240627 MGI PMID:22669107 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012706 decreased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20180201 MGI PMID:22383895 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0012724 absent head fold IAGP N RGD:5509061 20240627 MGI PMID:22669107 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20180201 MGI PMID:26921005 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20180201 MGI PMID:21693517 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20180201 MGI PMID:27179789 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0014078 small intestinal villus atrophy IAGP N RGD:5509061 20180201 MGI PMID:26232697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20180201 MGI PMID:26232697 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20181129 MGI PMID:27505251 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0014104 decreased chondrocyte apoptosis IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20180201 MGI PMID:26921005 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:22763239 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20180201 MGI PMID:22615579 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0020290 floppy ears IAGP N RGD:5509061 20181129 MGI PMID:27505251 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0020333 enhanced leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:19008446 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0020391 radial glial endfoot detachment IAGP N RGD:5509061 20180201 MGI PMID:23217742 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0030423 abnormal pinna cartilage morphology IAGP N RGD:5509061 20181129 MGI PMID:27505251 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0030538 abnormal notochordal plate morphology IAGP N RGD:5509061 20180201 MGI PMID:21693517 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0030798 joint contracture IAGP N RGD:5509061 20230323 MGI PMID:34767447 1557383 Edil3 EGF-like repeats and discoidin I-like domains 3 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:24895408 1557386 Cks2 CDC28 protein kinase regulatory subunit 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12714746 1557386 Cks2 CDC28 protein kinase regulatory subunit 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12714746 1557386 Cks2 CDC28 protein kinase regulatory subunit 2 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:12714746 1557386 Cks2 CDC28 protein kinase regulatory subunit 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:12714746 1557386 Cks2 CDC28 protein kinase regulatory subunit 2 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:12714746 1557386 Cks2 CDC28 protein kinase regulatory subunit 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12714746 1557386 Cks2 CDC28 protein kinase regulatory subunit 2 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:12714746 1557387 Zscan5b zinc finger and SCAN domain containing 5B gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1557387 Zscan5b zinc finger and SCAN domain containing 5B gene MP:0001406 abnormal gait IEA N RGD:5509061 20201022 MGI 1557387 Zscan5b zinc finger and SCAN domain containing 5B gene MP:0010095 increased chromosomal stability IAGP N RGD:5509061 20201001 MGI PMID:31155506 1557390 Pof1b premature ovarian failure 1B gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20221215 MGI 1557390 Pof1b premature ovarian failure 1B gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1557390 Pof1b premature ovarian failure 1B gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1557390 Pof1b premature ovarian failure 1B gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1557390 Pof1b premature ovarian failure 1B gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1557390 Pof1b premature ovarian failure 1B gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1557390 Pof1b premature ovarian failure 1B gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1557391 Spata16 spermatogenesis associated 16 gene MP:0001147 small testis IAGP N RGD:5509061 20180705 MGI PMID:29065458 1557391 Spata16 spermatogenesis associated 16 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20180705 MGI PMID:29065458 1557391 Spata16 spermatogenesis associated 16 gene MP:0001925 male infertility IAGP N RGD:5509061 20180705 MGI PMID:29065458 1557391 Spata16 spermatogenesis associated 16 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20180705 MGI PMID:29065458 1557391 Spata16 spermatogenesis associated 16 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20180705 MGI PMID:29065458 1557391 Spata16 spermatogenesis associated 16 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180705 MGI PMID:29065458 1557391 Spata16 spermatogenesis associated 16 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20180705 MGI PMID:29065458 1557391 Spata16 spermatogenesis associated 16 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20180705 MGI PMID:29065458 1557391 Spata16 spermatogenesis associated 16 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20180705 MGI PMID:29065458 1557391 Spata16 spermatogenesis associated 16 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20180705 MGI PMID:29065458 1557392 Hsfy2 heat shock transcription factor, Y-linked 2 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1557392 Hsfy2 heat shock transcription factor, Y-linked 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220519 MGI 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20160128 MGI PMID:26487682 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20160128 MGI PMID:26487682 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0001512 trunk curl IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0001954 respiratory distress IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0002083 premature death IAGP N RGD:5509061 20160128 MGI PMID:26487682 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0002083 premature death IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20160128 MGI PMID:26487682 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20160128 MGI PMID:26487682 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0002833 increased heart weight IAGP N RGD:5509061 20160128 MGI PMID:26487682 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0002833 increased heart weight IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20160128 MGI PMID:26487682 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20180614 MGI PMID:29078393 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20160128 MGI PMID:26487682 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0004146 absent M line IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0004937 dilated heart IAGP N RGD:5509061 20160128 MGI PMID:26487682 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160128 MGI PMID:26487682 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20160128 MGI PMID:26487682 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20160128 MGI PMID:26487682 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20161013 MGI PMID:27274810 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20160128 MGI PMID:26487682 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20180614 MGI PMID:29078393 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160128 MGI PMID:26487682 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180614 MGI PMID:29078393 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20160128 MGI PMID:26487682 1557393 Lmod2 leiomodin 2 (cardiac) gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:26487682 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15199160 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0003080 increased natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:15199160 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0003080 increased natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:16439675 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0003080 increased natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:18203684 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0003604 single kidney IEA N RGD:5509061 20230119 MGI 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0004819 decreased skeletal muscle mass IEA N RGD:5509061 20230119 MGI 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:18203684 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16439675 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:18203684 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0008559 abnormal interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16439675 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18203684 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18203684 1557394 Clnk cytokine-dependent hematopoietic cell linker gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:16439675 1557395 Snx12 sorting nexin 12 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1557395 Snx12 sorting nexin 12 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20220811 MGI 1557395 Snx12 sorting nexin 12 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1557395 Snx12 sorting nexin 12 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20230601 MGI 1557397 Lcor ligand dependent nuclear receptor corepressor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200514 MGI PMID:29628311 1557398 Tm2d3 TM2 domain containing 3 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20210128 MGI 1557398 Tm2d3 TM2 domain containing 3 gene MP:0001785 edema IEA N RGD:5509061 20220519 MGI 1557398 Tm2d3 TM2 domain containing 3 gene MP:0001914 hemorrhage IEA N RGD:5509061 20220519 MGI 1557398 Tm2d3 TM2 domain containing 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1557398 Tm2d3 TM2 domain containing 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557399 Acot4 acyl-CoA thioesterase 4 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1557402 Vit vitrin gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20170223 MGI PMID:25331329 1557402 Vit vitrin gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20170223 MGI PMID:25331329 1557402 Vit vitrin gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20170223 MGI PMID:25331329 1557402 Vit vitrin gene MP:0004100 abnormal spinal cord interneuron morphology IAGP N RGD:5509061 20170223 MGI PMID:25331329 1557402 Vit vitrin gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20170223 MGI PMID:25331329 1557402 Vit vitrin gene MP:0009688 abnormal spinal cord central canal morphology IAGP N RGD:5509061 20170223 MGI PMID:25331329 1557402 Vit vitrin gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20170223 MGI PMID:25331329 1557402 Vit vitrin gene MP:0010151 abnormal spinal cord ependymal layer morphology IAGP N RGD:5509061 20170223 MGI PMID:25331329 1557402 Vit vitrin gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20170223 MGI PMID:25331329 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0010360 decreased liver free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:22231784 1557405 Naa40 N(alpha)-acetyltransferase 40, NatD catalytic subunit gene MP:0031270 decreased susceptibility to age-related hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:22231784 1557406 Dct dopachrome tautomerase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:15060160 1557406 Dct dopachrome tautomerase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:18715234 1557406 Dct dopachrome tautomerase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:8530099 1557406 Dct dopachrome tautomerase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20211223 MGI PMID:33100333 1557406 Dct dopachrome tautomerase gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1557406 Dct dopachrome tautomerase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1557406 Dct dopachrome tautomerase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20181122 MGI PMID:20144786 1557406 Dct dopachrome tautomerase gene MP:0002939 head spot IAGP N RGD:5509061 20181122 MGI PMID:25818501 1557406 Dct dopachrome tautomerase gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20181122 MGI PMID:20144786 1557406 Dct dopachrome tautomerase gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18715234 1557406 Dct dopachrome tautomerase gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20211223 MGI PMID:33100333 1557406 Dct dopachrome tautomerase gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1557406 Dct dopachrome tautomerase gene MP:0010037 ectopic melanocytes IAGP N RGD:5509061 20181122 MGI PMID:20144786 1557406 Dct dopachrome tautomerase gene MP:0010192 abnormal retina melanin granule morphology IAGP N RGD:5509061 20211223 MGI PMID:33100333 1557406 Dct dopachrome tautomerase gene MP:0010206 pigment incontinence IAGP N RGD:5509061 20181129 MGI PMID:20144786 1557406 Dct dopachrome tautomerase gene MP:0011830 ectopic hair follicle melanin granules IAGP N RGD:5509061 20181122 MGI PMID:20144786 1557407 Zbtb33 zinc finger and BTB domain containing 33 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16354691 1557407 Zbtb33 zinc finger and BTB domain containing 33 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16354691 1557407 Zbtb33 zinc finger and BTB domain containing 33 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16354691 1557407 Zbtb33 zinc finger and BTB domain containing 33 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:16354691 1557408 G3bp1 G3BP stress granule assembly factor 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16166649 1557408 G3bp1 G3BP stress granule assembly factor 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:16166649 1557408 G3bp1 G3BP stress granule assembly factor 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:16166649 1557408 G3bp1 G3BP stress granule assembly factor 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1557408 G3bp1 G3BP stress granule assembly factor 1 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16166649 1557408 G3bp1 G3BP stress granule assembly factor 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16166649 1557408 G3bp1 G3BP stress granule assembly factor 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:16166649 1557408 G3bp1 G3BP stress granule assembly factor 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16166649 1557408 G3bp1 G3BP stress granule assembly factor 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:16166649 1557408 G3bp1 G3BP stress granule assembly factor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16166649 1557408 G3bp1 G3BP stress granule assembly factor 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1557408 G3bp1 G3BP stress granule assembly factor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16166649 1557408 G3bp1 G3BP stress granule assembly factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557408 G3bp1 G3BP stress granule assembly factor 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1557409 Cbx3 chromobox 3 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20423503 1557409 Cbx3 chromobox 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:20423503 1557409 Cbx3 chromobox 3 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:17644066 1557409 Cbx3 chromobox 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20423503 1557409 Cbx3 chromobox 3 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:20423503 1557409 Cbx3 chromobox 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20423503 1557409 Cbx3 chromobox 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20423503 1557411 Ppp6r2 protein phosphatase 6, regulatory subunit 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141218 MGI PMID:24440290 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:19884350 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141218 MGI PMID:24440290 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19884350 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:19884350 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:19884350 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:19884350 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:19884350 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0010924 abnormal osteoid morphology IAGP N RGD:5509061 20141003 MGI PMID:19884350 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0010927 decreased osteoid volume IAGP N RGD:5509061 20141003 MGI PMID:19884350 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0010930 decreased osteoid thickness IAGP N RGD:5509061 20141003 MGI PMID:19884350 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:21071677 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:19884350 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:19884350 1557413 Naca nascent polypeptide-associated complex alpha polypeptide gene MP:0030482 increased osteocyte number IAGP N RGD:5509061 20171221 MGI PMID:19884350 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20220519 MGI PMID:29178458 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20220519 MGI PMID:29178458 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:12807825 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16557300 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:16987502 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16987502 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:16987502 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21441458 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20220519 MGI PMID:29178458 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20220519 MGI PMID:29178458 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20220519 MGI PMID:29178458 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:11901205 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20220519 MGI PMID:29178458 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20220519 MGI PMID:29178458 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16987502 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11994431 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12807825 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:11994431 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12807825 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0005327 abnormal mesangial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16987502 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:16987502 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0008343 abnormal gamma-delta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21419662 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20220519 MGI PMID:29178458 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:11994431 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11994431 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21441458 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0009628 absent brachial lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0009634 absent popliteal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12070288 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20220519 MGI PMID:29178458 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:21441458 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20220519 MGI PMID:29178458 1557415 Tnfsf14 tumor necrosis factor (ligand) superfamily, member 14 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:16987502 1557416 Myof myoferlin gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:16280346 1557416 Myof myoferlin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16280346 1557416 Myof myoferlin gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:17702744 1557416 Myof myoferlin gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16280346 1557416 Myof myoferlin gene MP:0009408 decreased skeletal muscle fiber density IAGP N RGD:5509061 20141003 MGI PMID:16280346 1557416 Myof myoferlin gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:16280346 1557417 Gdf3 growth differentiation factor 3 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:16368929 1557417 Gdf3 growth differentiation factor 3 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:17936261 1557417 Gdf3 growth differentiation factor 3 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:16368929 1557417 Gdf3 growth differentiation factor 3 gene MP:0001687 thin endoderm IAGP N RGD:5509061 20141003 MGI PMID:16368929 1557417 Gdf3 growth differentiation factor 3 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19008465 1557417 Gdf3 growth differentiation factor 3 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:16368929 1557417 Gdf3 growth differentiation factor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17936261 1557417 Gdf3 growth differentiation factor 3 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:16368929 1557417 Gdf3 growth differentiation factor 3 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:17936261 1557417 Gdf3 growth differentiation factor 3 gene MP:0004713 split notochord IAGP N RGD:5509061 20141003 MGI PMID:16368929 1557417 Gdf3 growth differentiation factor 3 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16368929 1557417 Gdf3 growth differentiation factor 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19008465 1557417 Gdf3 growth differentiation factor 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19008465 1557417 Gdf3 growth differentiation factor 3 gene MP:0008533 abnormal anterior visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16368929 1557417 Gdf3 growth differentiation factor 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17936261 1557417 Gdf3 growth differentiation factor 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19008465 1557417 Gdf3 growth differentiation factor 3 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:19008465 1557417 Gdf3 growth differentiation factor 3 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19008465 1557417 Gdf3 growth differentiation factor 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16368929 1557417 Gdf3 growth differentiation factor 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19008465 1557417 Gdf3 growth differentiation factor 3 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17936261 1557417 Gdf3 growth differentiation factor 3 gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20141003 MGI PMID:16368929 1557417 Gdf3 growth differentiation factor 3 gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20141003 MGI PMID:17936261 1557417 Gdf3 growth differentiation factor 3 gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:16368929 1557417 Gdf3 growth differentiation factor 3 gene MP:0012156 rostral-caudal axis duplication IAGP N RGD:5509061 20141003 MGI PMID:16368929 1557417 Gdf3 growth differentiation factor 3 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:17936261 1557417 Gdf3 growth differentiation factor 3 gene MP:0012159 absent anterior visceral endoderm IAGP N RGD:5509061 20141003 MGI PMID:17936261 1557417 Gdf3 growth differentiation factor 3 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:17936261 1557417 Gdf3 growth differentiation factor 3 gene MP:0013207 absent endoderm IAGP N RGD:5509061 20141003 MGI PMID:16368929 1557418 Gpihbp1 GPI-anchored HDL-binding protein 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17403372 1557418 Gpihbp1 GPI-anchored HDL-binding protein 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17403372 1557418 Gpihbp1 GPI-anchored HDL-binding protein 1 gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17403372 1557418 Gpihbp1 GPI-anchored HDL-binding protein 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17403372 1557419 Col24a1 collagen, type XXIV, alpha 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1557419 Col24a1 collagen, type XXIV, alpha 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20160421 MGI 1557421 Asb10 ankyrin repeat and SOCS box-containing 10 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20210128 MGI 1557421 Asb10 ankyrin repeat and SOCS box-containing 10 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1557421 Asb10 ankyrin repeat and SOCS box-containing 10 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 1557422 Serpinb12 serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 12 gene MP:0001410 head bobbing IEA N RGD:5509061 20170105 MGI 1557422 Serpinb12 serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 12 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1557423 Ids iduronate 2-sulfatase gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:22704483 1557423 Ids iduronate 2-sulfatase gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16505002 1557423 Ids iduronate 2-sulfatase gene MP:0000414 alopecia IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0000414 alopecia IAGP N RGD:5509061 20201210 MGI PMID:20652491 1557423 Ids iduronate 2-sulfatase gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16505002 1557423 Ids iduronate 2-sulfatase gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20201210 MGI PMID:20652491 1557423 Ids iduronate 2-sulfatase gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20201210 MGI PMID:20652491 1557423 Ids iduronate 2-sulfatase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12572850 1557423 Ids iduronate 2-sulfatase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16505002 1557423 Ids iduronate 2-sulfatase gene MP:0001265 decreased body size IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0001296 macrophthalmia IAGP N RGD:5509061 20141003 MGI PMID:22704483 1557423 Ids iduronate 2-sulfatase gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16505002 1557423 Ids iduronate 2-sulfatase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16505002 1557423 Ids iduronate 2-sulfatase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20201210 MGI PMID:20652491 1557423 Ids iduronate 2-sulfatase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16505002 1557423 Ids iduronate 2-sulfatase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22704483 1557423 Ids iduronate 2-sulfatase gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:16505002 1557423 Ids iduronate 2-sulfatase gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:22704483 1557423 Ids iduronate 2-sulfatase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16505002 1557423 Ids iduronate 2-sulfatase gene MP:0002083 premature death IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0002083 premature death IAGP N RGD:5509061 20201210 MGI PMID:20652491 1557423 Ids iduronate 2-sulfatase gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:12572850 1557423 Ids iduronate 2-sulfatase gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:16505002 1557423 Ids iduronate 2-sulfatase gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:16505002 1557423 Ids iduronate 2-sulfatase gene MP:0002176 increased brain weight IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:12572850 1557423 Ids iduronate 2-sulfatase gene MP:0002832 coarse hair IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20201217 MGI PMID:22847837 1557423 Ids iduronate 2-sulfatase gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12572850 1557423 Ids iduronate 2-sulfatase gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0002936 joint swelling IAGP N RGD:5509061 20141003 MGI PMID:12572850 1557423 Ids iduronate 2-sulfatase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0002997 enlarged seminal vesicle IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20201210 MGI PMID:20652491 1557423 Ids iduronate 2-sulfatase gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20201217 MGI PMID:22847837 1557423 Ids iduronate 2-sulfatase gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20201210 MGI PMID:20652491 1557423 Ids iduronate 2-sulfatase gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22704483 1557423 Ids iduronate 2-sulfatase gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0004288 abnormal spiral ligament morphology IAGP N RGD:5509061 20201217 MGI PMID:22847837 1557423 Ids iduronate 2-sulfatase gene MP:0004308 abnormal basilar membrane morphology IAGP N RGD:5509061 20201217 MGI PMID:22847837 1557423 Ids iduronate 2-sulfatase gene MP:0004851 increased testis weight IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0004928 increased epididymis weight IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20141003 MGI PMID:12572850 1557423 Ids iduronate 2-sulfatase gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20141003 MGI PMID:16505002 1557423 Ids iduronate 2-sulfatase gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16505002 1557423 Ids iduronate 2-sulfatase gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0005630 increased lung weight IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0006018 abnormal tympanic membrane morphology IAGP N RGD:5509061 20201217 MGI PMID:22847837 1557423 Ids iduronate 2-sulfatase gene MP:0006021 abnormal Reissner membrane morphology IAGP N RGD:5509061 20201217 MGI PMID:22847837 1557423 Ids iduronate 2-sulfatase gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:22704483 1557423 Ids iduronate 2-sulfatase gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:22704483 1557423 Ids iduronate 2-sulfatase gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:16505002 1557423 Ids iduronate 2-sulfatase gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0009728 abnormal calcaneum morphology IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0009840 abnormal foam cell morphology IAGP N RGD:5509061 20201210 MGI PMID:20652491 1557423 Ids iduronate 2-sulfatase gene MP:0009877 exostosis IAGP N RGD:5509061 20141003 MGI PMID:22704483 1557423 Ids iduronate 2-sulfatase gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0011473 increased urine glycosaminoglycan level IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0011473 increased urine glycosaminoglycan level IAGP N RGD:5509061 20201210 MGI PMID:20652491 1557423 Ids iduronate 2-sulfatase gene MP:0011475 abnormal glycosaminoglycan level IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0011475 abnormal glycosaminoglycan level IAGP N RGD:5509061 20201210 MGI PMID:20652491 1557423 Ids iduronate 2-sulfatase gene MP:0011475 abnormal glycosaminoglycan level IAGP N RGD:5509061 20201217 MGI PMID:22847837 1557423 Ids iduronate 2-sulfatase gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20201217 MGI PMID:22847837 1557423 Ids iduronate 2-sulfatase gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0020169 increased thyroid gland weight IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0030068 large face IAGP N RGD:5509061 20201210 MGI PMID:20652491 1557423 Ids iduronate 2-sulfatase gene MP:0030074 coarse facial features IAGP N RGD:5509061 20170921 MGI PMID:22704483 1557423 Ids iduronate 2-sulfatase gene MP:0030074 coarse facial features IAGP N RGD:5509061 20201210 MGI PMID:20652491 1557423 Ids iduronate 2-sulfatase gene MP:0030188 round snout IAGP N RGD:5509061 20180118 MGI PMID:22704483 1557423 Ids iduronate 2-sulfatase gene MP:0030189 broad snout IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0030316 enlarged neurocranium IAGP N RGD:5509061 20180927 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0030410 middle ear effusion IAGP N RGD:5509061 20201217 MGI PMID:22847837 1557423 Ids iduronate 2-sulfatase gene MP:0030776 calcified calcaneal tendon IAGP N RGD:5509061 20181004 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0030808 abnormal hindlimb joint morphology IAGP N RGD:5509061 20181101 MGI PMID:17876721 1557423 Ids iduronate 2-sulfatase gene MP:0030808 abnormal hindlimb joint morphology IAGP N RGD:5509061 20201210 MGI PMID:20652491 1557423 Ids iduronate 2-sulfatase gene MP:0030811 abnormal hand joint morphology IAGP N RGD:5509061 20201210 MGI PMID:20652491 1557423 Ids iduronate 2-sulfatase gene MP:0030863 decreased joint mobility IAGP N RGD:5509061 20181101 MGI PMID:17876721 1557424 Arx aristaless related homeobox gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:14561778 1557424 Arx aristaless related homeobox gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0000243 myoclonus IAGP N RGD:5509061 20180913 MGI PMID:28602636 1557424 Arx aristaless related homeobox gene MP:0000743 muscle spasm IAGP N RGD:5509061 20180913 MGI PMID:29659809 1557424 Arx aristaless related homeobox gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:14561778 1557424 Arx aristaless related homeobox gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:18799476 1557424 Arx aristaless related homeobox gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18799476 1557424 Arx aristaless related homeobox gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:18799476 1557424 Arx aristaless related homeobox gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:19439424 1557424 Arx aristaless related homeobox gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:19439424 1557424 Arx aristaless related homeobox gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180913 MGI PMID:28602636 1557424 Arx aristaless related homeobox gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20180913 MGI PMID:28602636 1557424 Arx aristaless related homeobox gene MP:0001361 social withdrawal IAGP N RGD:5509061 20180913 MGI PMID:28602636 1557424 Arx aristaless related homeobox gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20180913 MGI PMID:28602636 1557424 Arx aristaless related homeobox gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180913 MGI PMID:28602636 1557424 Arx aristaless related homeobox gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0001406 abnormal gait IAGP N RGD:5509061 20180913 MGI PMID:29659809 1557424 Arx aristaless related homeobox gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20180913 MGI PMID:28602636 1557424 Arx aristaless related homeobox gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20180913 MGI PMID:28602636 1557424 Arx aristaless related homeobox gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:14561778 1557424 Arx aristaless related homeobox gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0001525 impaired balance IAGP N RGD:5509061 20180913 MGI PMID:29659809 1557424 Arx aristaless related homeobox gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:22056672 1557424 Arx aristaless related homeobox gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14561778 1557424 Arx aristaless related homeobox gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0002064 seizures IAGP N RGD:5509061 20180913 MGI PMID:28602636 1557424 Arx aristaless related homeobox gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20180913 MGI PMID:28602636 1557424 Arx aristaless related homeobox gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0002083 premature death IAGP N RGD:5509061 20180913 MGI PMID:28602636 1557424 Arx aristaless related homeobox gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18799476 1557424 Arx aristaless related homeobox gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20180913 MGI PMID:29659809 1557424 Arx aristaless related homeobox gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20180913 MGI PMID:29659809 1557424 Arx aristaless related homeobox gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0003247 abnormal glutaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:22056672 1557424 Arx aristaless related homeobox gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20180913 MGI PMID:28602636 1557424 Arx aristaless related homeobox gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20180913 MGI PMID:29659809 1557424 Arx aristaless related homeobox gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:14561778 1557424 Arx aristaless related homeobox gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20180913 MGI PMID:29659809 1557424 Arx aristaless related homeobox gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19439424 1557424 Arx aristaless related homeobox gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19439424 1557424 Arx aristaless related homeobox gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19439424 1557424 Arx aristaless related homeobox gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20180913 MGI PMID:29659809 1557424 Arx aristaless related homeobox gene MP:0004103 abnormal ventral striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:19439424 1557424 Arx aristaless related homeobox gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0005148 seminal vesicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0005218 abnormal pancreatic delta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14561778 1557424 Arx aristaless related homeobox gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20180913 MGI PMID:29659809 1557424 Arx aristaless related homeobox gene MP:0006308 enlarged seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0008269 abnormal hippocampus CA4 region morphology IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19439424 1557424 Arx aristaless related homeobox gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0008929 abnormal central medial nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20180913 MGI PMID:29659809 1557424 Arx aristaless related homeobox gene MP:0009178 absent pancreatic alpha cells IAGP N RGD:5509061 20141003 MGI PMID:14561778 1557424 Arx aristaless related homeobox gene MP:0009180 increased pancreatic delta cell number IAGP N RGD:5509061 20141003 MGI PMID:14561778 1557424 Arx aristaless related homeobox gene MP:0009324 absent hippocampal fimbria IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20180913 MGI PMID:29659809 1557424 Arx aristaless related homeobox gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19587282 1557424 Arx aristaless related homeobox gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14561778 1557424 Arx aristaless related homeobox gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19439424 1557424 Arx aristaless related homeobox gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180913 MGI PMID:28602636 1557424 Arx aristaless related homeobox gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19605412 1557424 Arx aristaless related homeobox gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20180913 MGI PMID:28602636 1557424 Arx aristaless related homeobox gene MP:0013603 abnormal fetal Leydig cell differentiation IAGP N RGD:5509061 20150319 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0014558 decreased cortical ventricular zone thickness IAGP N RGD:5509061 20241031 MGI PMID:12379852 1557424 Arx aristaless related homeobox gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20180913 MGI PMID:28602636 1557424 Arx aristaless related homeobox gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:29659809 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:15294946 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15294936 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15294936 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15294946 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:17073941 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15294936 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15294946 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21300983 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21228330 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16973390 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0002491 decreased IgD level IAGP N RGD:5509061 20141003 MGI PMID:15294946 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21228330 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15368291 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:15368291 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:16973390 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15294946 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17073941 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17073941 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15368291 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16782029 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21300983 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17073941 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:15294936 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:15294946 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21228330 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:15294936 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:15294946 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15294936 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21228330 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008216 absent transitional stage B cells IAGP N RGD:5509061 20141003 MGI PMID:15294946 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:21300983 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15294936 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15294946 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:15294936 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:15294936 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:15294936 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15368291 1557427 Tnfrsf13c tumor necrosis factor receptor superfamily, member 13c gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21228330 1557428 Enox2 ecto-NOX disulfide-thiol exchanger 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1557429 Cd209e CD209e antigen gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1557430 Glt8d2 glycosyltransferase 8 domain containing 2 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1557430 Glt8d2 glycosyltransferase 8 domain containing 2 gene MP:0002420 abnormal adaptive immunity IEA N RGD:5509061 20170413 MGI 1557430 Glt8d2 glycosyltransferase 8 domain containing 2 gene MP:0008495 decreased IgG1 level IEA N RGD:5509061 20170413 MGI 1557430 Glt8d2 glycosyltransferase 8 domain containing 2 gene MP:0008496 decreased IgG2a level IEA N RGD:5509061 20170413 MGI 1557430 Glt8d2 glycosyltransferase 8 domain containing 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1557430 Glt8d2 glycosyltransferase 8 domain containing 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20150430 MGI 1557431 Sertad2 SERTA domain containing 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0004892 increased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0009127 increased brown fat cell number IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0011016 increased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:16721052 1557431 Sertad2 SERTA domain containing 2 gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:23291629 1557431 Sertad2 SERTA domain containing 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:23291629 1557432 Pdk3 pyruvate dehydrogenase kinase, isoenzyme 3 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20210610 MGI PMID:33773101 1557432 Pdk3 pyruvate dehydrogenase kinase, isoenzyme 3 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20210610 MGI PMID:33773101 1557432 Pdk3 pyruvate dehydrogenase kinase, isoenzyme 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20210610 MGI PMID:33773101 1557432 Pdk3 pyruvate dehydrogenase kinase, isoenzyme 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210610 MGI PMID:33773101 1557432 Pdk3 pyruvate dehydrogenase kinase, isoenzyme 3 gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20210610 MGI PMID:33773101 1557434 Hopx HOP homeobox gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:12297046 1557434 Hopx HOP homeobox gene MP:0000275 heart hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12297046 1557434 Hopx HOP homeobox gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:16510470 1557434 Hopx HOP homeobox gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16510470 1557434 Hopx HOP homeobox gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12297046 1557434 Hopx HOP homeobox gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12297046 1557434 Hopx HOP homeobox gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12297046 1557434 Hopx HOP homeobox gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:12297046 1557434 Hopx HOP homeobox gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16510470 1557434 Hopx HOP homeobox gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:12297045 1557434 Hopx HOP homeobox gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:12297046 1557434 Hopx HOP homeobox gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12297046 1557434 Hopx HOP homeobox gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:12297046 1557434 Hopx HOP homeobox gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12297046 1557434 Hopx HOP homeobox gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:15790958 1557434 Hopx HOP homeobox gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12297046 1557434 Hopx HOP homeobox gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:12297045 1557434 Hopx HOP homeobox gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:15790958 1557434 Hopx HOP homeobox gene MP:0004072 abnormal frontal plane axis IAGP N RGD:5509061 20141003 MGI PMID:15790958 1557434 Hopx HOP homeobox gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12297046 1557434 Hopx HOP homeobox gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:12297046 1557434 Hopx HOP homeobox gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:12297045 1557434 Hopx HOP homeobox gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12297045 1557434 Hopx HOP homeobox gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12975471 1557434 Hopx HOP homeobox gene MP:0005586 decreased tidal volume IAGP N RGD:5509061 20141003 MGI PMID:16510470 1557434 Hopx HOP homeobox gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:16510470 1557434 Hopx HOP homeobox gene MP:0006321 increased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:12975471 1557434 Hopx HOP homeobox gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:15790958 1557434 Hopx HOP homeobox gene MP:0010553 prolonged HV interval IAGP N RGD:5509061 20141003 MGI PMID:15790958 1557434 Hopx HOP homeobox gene MP:0010560 intraventricular block IAGP N RGD:5509061 20141003 MGI PMID:15790958 1557434 Hopx HOP homeobox gene MP:0010992 increased surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:16510470 1557434 Hopx HOP homeobox gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16510470 1557434 Hopx HOP homeobox gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16510470 1557434 Hopx HOP homeobox gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12297045 1557434 Hopx HOP homeobox gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12297046 1557434 Hopx HOP homeobox gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12975471 1557434 Hopx HOP homeobox gene MP:0011142 abnormal lung-associated mesenchyme development IAGP N RGD:5509061 20141003 MGI PMID:16510470 1557434 Hopx HOP homeobox gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:16510470 1557436 Mob2 MOB kinase activator 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210520 MGI 1557436 Mob2 MOB kinase activator 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557438 Cpvl carboxypeptidase, vitellogenic-like gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1557438 Cpvl carboxypeptidase, vitellogenic-like gene MP:0001200 thick skin IEA N RGD:5509061 20181227 MGI 1557438 Cpvl carboxypeptidase, vitellogenic-like gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1557438 Cpvl carboxypeptidase, vitellogenic-like gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 1557438 Cpvl carboxypeptidase, vitellogenic-like gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19884347 1557444 Akap17b A kinase anchor protein 17B gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20111116 MGI 1557444 Akap17b A kinase anchor protein 17B gene MP:0001698 decreased embryo size IEA N RGD:5509061 20111116 MGI 1557444 Akap17b A kinase anchor protein 17B gene MP:0002084 abnormal developmental patterning IEA N RGD:5509061 20111116 MGI 1557444 Akap17b A kinase anchor protein 17B gene MP:0002085 abnormal embryonic tissue morphology IEA N RGD:5509061 20111116 MGI 1557444 Akap17b A kinase anchor protein 17B gene MP:0003400 kinked neural tube IEA N RGD:5509061 20111116 MGI 1557444 Akap17b A kinase anchor protein 17B gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20111116 MGI 1557444 Akap17b A kinase anchor protein 17B gene MP:0009657 failure of chorioallantoic fusion IEA N RGD:5509061 20111116 MGI 1557444 Akap17b A kinase anchor protein 17B gene MP:0009768 impaired somite development IEA N RGD:5509061 20111116 MGI 1557444 Akap17b A kinase anchor protein 17B gene MP:0011732 decreased somite size IEA N RGD:5509061 20141003 MGI 1557446 Klhl42 kelch-like 42 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1557446 Klhl42 kelch-like 42 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20181227 MGI 1557446 Klhl42 kelch-like 42 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:23583643 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23583643 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15917799 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22700722 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23583643 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23583643 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:23583642 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15917799 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:23583643 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23583642 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:23583642 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15917799 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22700722 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23583642 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15917799 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:22700722 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:23583643 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23583642 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:23583643 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22700722 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:23583643 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:15917799 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:15917799 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:23583642 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:15917799 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:15917799 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22700722 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23583643 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23583643 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23583642 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23583643 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23583643 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:23583643 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:23583643 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:22700722 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:23583642 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0008895 abnormal intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20141003 MGI PMID:23451046 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:22700722 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:23583642 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:23583643 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0010189 abnormal T follicular helper cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22700722 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22700722 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23583642 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21844204 1557447 Rc3h1 RING CCCH (C3H) domains 1 gene MP:0031301 chronic liver inflammation IAGP N RGD:5509061 20211028 MGI PMID:23451046 1557448 Top2b topoisomerase (DNA) II beta gene MP:0000111 cleft palate IEA N RGD:5509061 20230119 MGI 1557448 Top2b topoisomerase (DNA) II beta gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10615047 1557448 Top2b topoisomerase (DNA) II beta gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20230119 MGI 1557448 Top2b topoisomerase (DNA) II beta gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1557448 Top2b topoisomerase (DNA) II beta gene MP:0000692 small spleen IEA N RGD:5509061 20230119 MGI 1557448 Top2b topoisomerase (DNA) II beta gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:10615047 1557448 Top2b topoisomerase (DNA) II beta gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:10615047 1557448 Top2b topoisomerase (DNA) II beta gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20200109 MGI PMID:28370415 1557448 Top2b topoisomerase (DNA) II beta gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20200109 MGI PMID:28370415 1557448 Top2b topoisomerase (DNA) II beta gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:10615047 1557448 Top2b topoisomerase (DNA) II beta gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 1557448 Top2b topoisomerase (DNA) II beta gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10615047 1557448 Top2b topoisomerase (DNA) II beta gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230119 MGI 1557448 Top2b topoisomerase (DNA) II beta gene MP:0001785 edema IEA N RGD:5509061 20230119 MGI 1557448 Top2b topoisomerase (DNA) II beta gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10615047 1557448 Top2b topoisomerase (DNA) II beta gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1557448 Top2b topoisomerase (DNA) II beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20200109 MGI PMID:28370415 1557448 Top2b topoisomerase (DNA) II beta gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20200109 MGI PMID:28370415 1557448 Top2b topoisomerase (DNA) II beta gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1557448 Top2b topoisomerase (DNA) II beta gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20200109 MGI PMID:28370415 1557448 Top2b topoisomerase (DNA) II beta gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0008285 abnormal hippocampus granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0008442 disorganized cortical plate IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0008443 absent subplate IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20200109 MGI PMID:28370415 1557448 Top2b topoisomerase (DNA) II beta gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20200109 MGI PMID:28370415 1557448 Top2b topoisomerase (DNA) II beta gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200109 MGI PMID:28370415 1557448 Top2b topoisomerase (DNA) II beta gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20200109 MGI PMID:28370415 1557448 Top2b topoisomerase (DNA) II beta gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200109 MGI PMID:28370415 1557448 Top2b topoisomerase (DNA) II beta gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20200109 MGI PMID:28370415 1557448 Top2b topoisomerase (DNA) II beta gene MP:0010236 abnormal retina outer limiting membrane morphology IAGP N RGD:5509061 20200109 MGI PMID:28370415 1557448 Top2b topoisomerase (DNA) II beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10615047 1557448 Top2b topoisomerase (DNA) II beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12773624 1557448 Top2b topoisomerase (DNA) II beta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1557448 Top2b topoisomerase (DNA) II beta gene MP:0011495 abnormal head shape IEA N RGD:5509061 20230601 MGI 1557451 Strip1 striatin interacting protein 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20180329 MGI PMID:29203676 1557451 Strip1 striatin interacting protein 1 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20180329 MGI PMID:29203676 1557451 Strip1 striatin interacting protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180329 MGI PMID:29203676 1557451 Strip1 striatin interacting protein 1 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20180329 MGI PMID:29203676 1557451 Strip1 striatin interacting protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180329 MGI PMID:29203676 1557451 Strip1 striatin interacting protein 1 gene MP:0011257 abnormal head fold morphology IAGP N RGD:5509061 20180329 MGI PMID:29203676 1557451 Strip1 striatin interacting protein 1 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20180329 MGI PMID:29203676 1557451 Strip1 striatin interacting protein 1 gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20180329 MGI PMID:29203676 1557451 Strip1 striatin interacting protein 1 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20180329 MGI PMID:29203676 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220811 MGI 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20200130 MGI PMID:23857330 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20200130 MGI PMID:23857330 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20200130 MGI PMID:23857330 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20200130 MGI PMID:23857330 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200130 MGI PMID:23857330 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20200130 MGI PMID:23857330 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20200130 MGI PMID:23857330 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20200130 MGI PMID:23857330 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20230601 MGI 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20200130 MGI PMID:23857330 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20190221 MGI PMID:23812712 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20200130 MGI PMID:23857330 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20200130 MGI PMID:23857330 1557452 Cox7a2l cytochrome c oxidase subunit 7A2 like gene MP:0020520 whitened brown adipose tissue morphology IAGP N RGD:5509061 20200130 MGI PMID:23857330 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20181227 MGI 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20181227 MGI 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20181227 MGI 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20181227 MGI 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20181227 MGI 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20181227 MGI 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1557454 Pcgf1 polycomb group ring finger 1 gene MP:0014484 decreased feces water content IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557455 Hoxa7 homeobox A7 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9784603 1557455 Hoxa7 homeobox A7 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:9784603 1557455 Hoxa7 homeobox A7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9784603 1557457 Kbtbd8 kelch repeat and BTB (POZ) domain containing 8 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1557457 Kbtbd8 kelch repeat and BTB (POZ) domain containing 8 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1557457 Kbtbd8 kelch repeat and BTB (POZ) domain containing 8 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1557457 Kbtbd8 kelch repeat and BTB (POZ) domain containing 8 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1557457 Kbtbd8 kelch repeat and BTB (POZ) domain containing 8 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1557457 Kbtbd8 kelch repeat and BTB (POZ) domain containing 8 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1557457 Kbtbd8 kelch repeat and BTB (POZ) domain containing 8 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1557457 Kbtbd8 kelch repeat and BTB (POZ) domain containing 8 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 1557457 Kbtbd8 kelch repeat and BTB (POZ) domain containing 8 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1557457 Kbtbd8 kelch repeat and BTB (POZ) domain containing 8 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1557459 Noto notochord homeobox gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:13837681 1557459 Noto notochord homeobox gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:22357932 1557459 Noto notochord homeobox gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:13837681 1557459 Noto notochord homeobox gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:15231714 1557459 Noto notochord homeobox gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:19720144 1557459 Noto notochord homeobox gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:22357932 1557459 Noto notochord homeobox gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:13837681 1557459 Noto notochord homeobox gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:15231714 1557459 Noto notochord homeobox gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:13837681 1557459 Noto notochord homeobox gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:13837681 1557459 Noto notochord homeobox gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:13837681 1557459 Noto notochord homeobox gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:13837681 1557459 Noto notochord homeobox gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:13837681 1557459 Noto notochord homeobox gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:22357932 1557459 Noto notochord homeobox gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:13837681 1557459 Noto notochord homeobox gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15231714 1557459 Noto notochord homeobox gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:13837681 1557459 Noto notochord homeobox gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:19720144 1557459 Noto notochord homeobox gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:19720144 1557459 Noto notochord homeobox gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:19720144 1557459 Noto notochord homeobox gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:22357932 1557459 Noto notochord homeobox gene MP:0004131 abnormal motile primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:22357932 1557459 Noto notochord homeobox gene MP:0004612 fusion of vertebral bodies IAGP N RGD:5509061 20141003 MGI PMID:13837681 1557459 Noto notochord homeobox gene MP:0004645 decreased vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:15231714 1557459 Noto notochord homeobox gene MP:0004645 decreased vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:8155581 1557459 Noto notochord homeobox gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:13837681 1557459 Noto notochord homeobox gene MP:0004714 truncated notochord IAGP N RGD:5509061 20141003 MGI PMID:13837681 1557459 Noto notochord homeobox gene MP:0004714 truncated notochord IAGP N RGD:5509061 20141003 MGI PMID:15231714 1557459 Noto notochord homeobox gene MP:0004714 truncated notochord IAGP N RGD:5509061 20141003 MGI PMID:15550757 1557459 Noto notochord homeobox gene MP:0004714 truncated notochord IAGP N RGD:5509061 20141003 MGI PMID:8155581 1557459 Noto notochord homeobox gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:13837681 1557459 Noto notochord homeobox gene MP:0008933 abnormal motile primary cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:22357932 1557459 Noto notochord homeobox gene MP:0011998 decreased embryonic cilium length IAGP N RGD:5509061 20141003 MGI PMID:22357932 1557459 Noto notochord homeobox gene MP:0012027 abnormal embryonic cilium location or orientation IAGP N RGD:5509061 20141003 MGI PMID:22357932 1557459 Noto notochord homeobox gene MP:0012093 absent nodal flow IAGP N RGD:5509061 20141003 MGI PMID:22357932 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0001805 decreased IgG level IEA N RGD:5509061 20161201 MGI 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23267016 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20151217 MGI PMID:24492962 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:23267016 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20151217 MGI PMID:24492962 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:23267016 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:23267016 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23267016 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008122 decreased myeloid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23267016 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20151217 MGI PMID:24492962 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267016 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008188 abnormal transitional stage B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23267016 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267016 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:23267016 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0008524 increased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23267016 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267016 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0010228 decreased transitional stage T3 B cell number IAGP N RGD:5509061 20141003 MGI PMID:23267016 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0010675 decreased activation-induced B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23267013 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:23267015 1557460 Sppl2a signal peptide peptidase like 2A gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20161201 MGI 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:18974357 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:18974357 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:21045827 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0000754 paresis IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:21045827 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:21045827 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21045827 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:21045827 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:21045827 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18974357 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25030553 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:18974357 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18974357 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0002989 small kidney IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:21045827 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0003606 kidney failure IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18974357 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20201022 MGI 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:21045827 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21045827 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0008812 abnormal rostrocaudal coat patterning IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18974357 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:18974357 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21045827 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:21045827 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21045827 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18974357 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18974357 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0011436 decreased urine magnesium level IAGP N RGD:5509061 20141003 MGI PMID:21045827 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0011979 abnormal magnesium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21045827 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0012024 abnormal nephron morphogenesis IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0012025 abnormal comma shaped body morphology IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0012026 abnormal S-shaped body morphology IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0012367 decreased erythrocyte magnesium level IAGP N RGD:5509061 20141003 MGI PMID:21045827 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1557461 Trpm7 transient receptor potential cation channel, subfamily M, member 7 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20181115 MGI PMID:22203997 1557464 Cers6 ceramide synthase 6 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:23760501 1557464 Cers6 ceramide synthase 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23760501 1557464 Cers6 ceramide synthase 6 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:23760501 1557464 Cers6 ceramide synthase 6 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20150101 MGI PMID:25295788 1557464 Cers6 ceramide synthase 6 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23760501 1557464 Cers6 ceramide synthase 6 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:23760501 1557464 Cers6 ceramide synthase 6 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20150101 MGI PMID:25295788 1557464 Cers6 ceramide synthase 6 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20150101 MGI PMID:25295788 1557464 Cers6 ceramide synthase 6 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20150101 MGI PMID:25295788 1557464 Cers6 ceramide synthase 6 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20150101 MGI PMID:25295788 1557464 Cers6 ceramide synthase 6 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20150101 MGI PMID:25295788 1557464 Cers6 ceramide synthase 6 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20150101 MGI PMID:25295788 1557464 Cers6 ceramide synthase 6 gene MP:0008912 nervous IAGP N RGD:5509061 20141003 MGI PMID:23760501 1557464 Cers6 ceramide synthase 6 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23760501 1557464 Cers6 ceramide synthase 6 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20150101 MGI PMID:25295788 1557464 Cers6 ceramide synthase 6 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20150101 MGI PMID:25295788 1557464 Cers6 ceramide synthase 6 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20150101 MGI PMID:25295788 1557464 Cers6 ceramide synthase 6 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20150101 MGI PMID:25295788 1557464 Cers6 ceramide synthase 6 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20141003 MGI PMID:23760501 1557464 Cers6 ceramide synthase 6 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20150101 MGI PMID:25295788 1557464 Cers6 ceramide synthase 6 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:25295788 1557464 Cers6 ceramide synthase 6 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:23760501 1557465 Dzip3 DAZ interacting protein 3, zinc finger gene MP:0008762 embryonic lethality IEA N RGD:5509061 20141003 MGI 1557466 Phox2b paired-like homeobox 2b gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:10736201 1557466 Phox2b paired-like homeobox 2b gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557466 Phox2b paired-like homeobox 2b gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20141003 MGI PMID:14627719 1557466 Phox2b paired-like homeobox 2b gene MP:0000906 abnormal trigeminal V mesencephalic nucleus morphology IAGP N RGD:5509061 20221215 MGI PMID:25975378 1557466 Phox2b paired-like homeobox 2b gene MP:0000910 small facial motor nucleus IAGP N RGD:5509061 20141003 MGI PMID:16319924 1557466 Phox2b paired-like homeobox 2b gene MP:0000910 small facial motor nucleus IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10360575 1557466 Phox2b paired-like homeobox 2b gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10704382 1557466 Phox2b paired-like homeobox 2b gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16319924 1557466 Phox2b paired-like homeobox 2b gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20133851 1557466 Phox2b paired-like homeobox 2b gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10360575 1557466 Phox2b paired-like homeobox 2b gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0001034 abnormal parasympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10360575 1557466 Phox2b paired-like homeobox 2b gene MP:0001034 abnormal parasympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16319924 1557466 Phox2b paired-like homeobox 2b gene MP:0001034 abnormal parasympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20133851 1557466 Phox2b paired-like homeobox 2b gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:16319924 1557466 Phox2b paired-like homeobox 2b gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:10360575 1557466 Phox2b paired-like homeobox 2b gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10704382 1557466 Phox2b paired-like homeobox 2b gene MP:0001066 absent trigeminal nerve IAGP N RGD:5509061 20141003 MGI PMID:10704382 1557466 Phox2b paired-like homeobox 2b gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20221215 MGI PMID:25975378 1557466 Phox2b paired-like homeobox 2b gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10704382 1557466 Phox2b paired-like homeobox 2b gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20221215 MGI PMID:25975378 1557466 Phox2b paired-like homeobox 2b gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:10360575 1557466 Phox2b paired-like homeobox 2b gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:14627719 1557466 Phox2b paired-like homeobox 2b gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:16319924 1557466 Phox2b paired-like homeobox 2b gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10360575 1557466 Phox2b paired-like homeobox 2b gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:14627719 1557466 Phox2b paired-like homeobox 2b gene MP:0001084 abnormal petrosal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:14627719 1557466 Phox2b paired-like homeobox 2b gene MP:0001086 absent petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:20133851 1557466 Phox2b paired-like homeobox 2b gene MP:0001087 abnormal nodose ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:14627719 1557466 Phox2b paired-like homeobox 2b gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:16319924 1557466 Phox2b paired-like homeobox 2b gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10360575 1557466 Phox2b paired-like homeobox 2b gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10360575 1557466 Phox2b paired-like homeobox 2b gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16319924 1557466 Phox2b paired-like homeobox 2b gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19940179 1557466 Phox2b paired-like homeobox 2b gene MP:0001265 decreased body size IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557466 Phox2b paired-like homeobox 2b gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20221215 MGI PMID:25975378 1557466 Phox2b paired-like homeobox 2b gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:18198276 1557466 Phox2b paired-like homeobox 2b gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0001575 cyanosis IAGP N RGD:5509061 20221215 MGI PMID:25975378 1557466 Phox2b paired-like homeobox 2b gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557466 Phox2b paired-like homeobox 2b gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20141003 MGI PMID:18198276 1557466 Phox2b paired-like homeobox 2b gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:18198276 1557466 Phox2b paired-like homeobox 2b gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:19940179 1557466 Phox2b paired-like homeobox 2b gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:18198276 1557466 Phox2b paired-like homeobox 2b gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:18198276 1557466 Phox2b paired-like homeobox 2b gene MP:0001953 respiratory failure IAGP N RGD:5509061 20221215 MGI PMID:25975378 1557466 Phox2b paired-like homeobox 2b gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:18198276 1557466 Phox2b paired-like homeobox 2b gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11929848 1557466 Phox2b paired-like homeobox 2b gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11929848 1557466 Phox2b paired-like homeobox 2b gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:16319924 1557466 Phox2b paired-like homeobox 2b gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19940179 1557466 Phox2b paired-like homeobox 2b gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20221215 MGI PMID:25975378 1557466 Phox2b paired-like homeobox 2b gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20221215 MGI PMID:25975378 1557466 Phox2b paired-like homeobox 2b gene MP:0002321 hypoventilation IAGP N RGD:5509061 20141003 MGI PMID:18198276 1557466 Phox2b paired-like homeobox 2b gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20141003 MGI PMID:21900566 1557466 Phox2b paired-like homeobox 2b gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0002338 abnormal pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:14627719 1557466 Phox2b paired-like homeobox 2b gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:11929848 1557466 Phox2b paired-like homeobox 2b gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:15150159 1557466 Phox2b paired-like homeobox 2b gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557466 Phox2b paired-like homeobox 2b gene MP:0002751 abnormal autonomic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:10360575 1557466 Phox2b paired-like homeobox 2b gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20221215 MGI PMID:25975378 1557466 Phox2b paired-like homeobox 2b gene MP:0003029 alkalemia IAGP N RGD:5509061 20141003 MGI PMID:21900566 1557466 Phox2b paired-like homeobox 2b gene MP:0003437 abnormal carotid body morphology IAGP N RGD:5509061 20141003 MGI PMID:14627719 1557466 Phox2b paired-like homeobox 2b gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:16319924 1557466 Phox2b paired-like homeobox 2b gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:19940179 1557466 Phox2b paired-like homeobox 2b gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:16319924 1557466 Phox2b paired-like homeobox 2b gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20141003 MGI PMID:10736201 1557466 Phox2b paired-like homeobox 2b gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16319924 1557466 Phox2b paired-like homeobox 2b gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20221215 MGI PMID:25975378 1557466 Phox2b paired-like homeobox 2b gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557466 Phox2b paired-like homeobox 2b gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:10360575 1557466 Phox2b paired-like homeobox 2b gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:10736201 1557466 Phox2b paired-like homeobox 2b gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:16319924 1557466 Phox2b paired-like homeobox 2b gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557466 Phox2b paired-like homeobox 2b gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18198276 1557466 Phox2b paired-like homeobox 2b gene MP:0004186 abnormal area postrema morphology IAGP N RGD:5509061 20141003 MGI PMID:14627719 1557466 Phox2b paired-like homeobox 2b gene MP:0004561 absent facial nerve IAGP N RGD:5509061 20141003 MGI PMID:10704382 1557466 Phox2b paired-like homeobox 2b gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19940179 1557466 Phox2b paired-like homeobox 2b gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0004990 abnormal ciliary ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15150159 1557466 Phox2b paired-like homeobox 2b gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20221215 MGI PMID:25975378 1557466 Phox2b paired-like homeobox 2b gene MP:0005576 decreased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:14627719 1557466 Phox2b paired-like homeobox 2b gene MP:0005576 decreased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:21900566 1557466 Phox2b paired-like homeobox 2b gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557466 Phox2b paired-like homeobox 2b gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:15150159 1557466 Phox2b paired-like homeobox 2b gene MP:0006276 abnormal autonomic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:21900566 1557466 Phox2b paired-like homeobox 2b gene MP:0008314 abnormal pterygopalatine ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20133851 1557466 Phox2b paired-like homeobox 2b gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557466 Phox2b paired-like homeobox 2b gene MP:0008947 increased neuron number IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557466 Phox2b paired-like homeobox 2b gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557466 Phox2b paired-like homeobox 2b gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19940179 1557466 Phox2b paired-like homeobox 2b gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19940179 1557466 Phox2b paired-like homeobox 2b gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18198276 1557466 Phox2b paired-like homeobox 2b gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21900566 1557466 Phox2b paired-like homeobox 2b gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221215 MGI PMID:25975378 1557466 Phox2b paired-like homeobox 2b gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16319924 1557466 Phox2b paired-like homeobox 2b gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19940179 1557466 Phox2b paired-like homeobox 2b gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10736201 1557466 Phox2b paired-like homeobox 2b gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10736201 1557466 Phox2b paired-like homeobox 2b gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11929848 1557466 Phox2b paired-like homeobox 2b gene MP:0011406 abnormal retrotrapezoid nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:20133877 1557466 Phox2b paired-like homeobox 2b gene MP:0011406 abnormal retrotrapezoid nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:21900566 1557466 Phox2b paired-like homeobox 2b gene MP:0011406 abnormal retrotrapezoid nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0011406 abnormal retrotrapezoid nucleus morphology IAGP N RGD:5509061 20221215 MGI PMID:25975378 1557466 Phox2b paired-like homeobox 2b gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0013002 decreased enteric neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0013005 decreased enteric neural crest cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0013006 abnormal enteric neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:22922260 1557466 Phox2b paired-like homeobox 2b gene MP:0014484 decreased feces water content IAGP N RGD:5509061 20241017 MGI PMID:37452641 1557467 Prdm2 PR domain containing 2, with ZNF domain gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11544182 1557467 Prdm2 PR domain containing 2, with ZNF domain gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11544182 1557467 Prdm2 PR domain containing 2, with ZNF domain gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11544182 1557467 Prdm2 PR domain containing 2, with ZNF domain gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11544182 1557467 Prdm2 PR domain containing 2, with ZNF domain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11544182 1557467 Prdm2 PR domain containing 2, with ZNF domain gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11544182 1557467 Prdm2 PR domain containing 2, with ZNF domain gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11544182 1557468 Dcaf6 DDB1 and CUL4 associated factor 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20191114 MGI PMID:26430214 1557468 Dcaf6 DDB1 and CUL4 associated factor 6 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20191114 MGI PMID:26430214 1557468 Dcaf6 DDB1 and CUL4 associated factor 6 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20191114 MGI PMID:26430214 1557468 Dcaf6 DDB1 and CUL4 associated factor 6 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20191114 MGI PMID:26430214 1557468 Dcaf6 DDB1 and CUL4 associated factor 6 gene MP:0031328 delayed skeletal muscle regeneration IAGP N RGD:5509061 20220106 MGI PMID:26430214 1557469 Ptpn13 protein tyrosine phosphatase, non-receptor type 13 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15226483 1557469 Ptpn13 protein tyrosine phosphatase, non-receptor type 13 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:15226483 1557469 Ptpn13 protein tyrosine phosphatase, non-receptor type 13 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17306571 1557469 Ptpn13 protein tyrosine phosphatase, non-receptor type 13 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17306571 1557469 Ptpn13 protein tyrosine phosphatase, non-receptor type 13 gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15932596 1557469 Ptpn13 protein tyrosine phosphatase, non-receptor type 13 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:15226483 1557469 Ptpn13 protein tyrosine phosphatase, non-receptor type 13 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17306571 1557469 Ptpn13 protein tyrosine phosphatase, non-receptor type 13 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17306571 1557469 Ptpn13 protein tyrosine phosphatase, non-receptor type 13 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15932596 1557469 Ptpn13 protein tyrosine phosphatase, non-receptor type 13 gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:19107198 1557471 Atpsckmt ATP synthase C subunit lysine N-methyltransferase gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20240328 MGI PMID:37944527 1557471 Atpsckmt ATP synthase C subunit lysine N-methyltransferase gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20240328 MGI PMID:37944527 1557471 Atpsckmt ATP synthase C subunit lysine N-methyltransferase gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20240328 MGI PMID:37944527 1557471 Atpsckmt ATP synthase C subunit lysine N-methyltransferase gene MP:0020879 abnormal calcium level IAGP N RGD:5509061 20240328 MGI PMID:37944527 1557471 Atpsckmt ATP synthase C subunit lysine N-methyltransferase gene MP:0020955 increased mechanical nociceptive threshold IAGP N RGD:5509061 20240328 MGI PMID:37944527 1557473 Myo6 myosin VI gene MP:0000032 cochlear degeneration IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20160929 MGI PMID:27534441 1557473 Myo6 myosin VI gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:12966030 1557473 Myo6 myosin VI gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:7493015 1557473 Myo6 myosin VI gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20180621 MGI PMID:20224170 1557473 Myo6 myosin VI gene MP:0000044 absent organ of Corti IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200514 MGI 1557473 Myo6 myosin VI gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1557473 Myo6 myosin VI gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220519 MGI 1557473 Myo6 myosin VI gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20220519 MGI 1557473 Myo6 myosin VI gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220519 MGI 1557473 Myo6 myosin VI gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1557473 Myo6 myosin VI gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12966030 1557473 Myo6 myosin VI gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20201022 MGI 1557473 Myo6 myosin VI gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10900098 1557473 Myo6 myosin VI gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:15978262 1557473 Myo6 myosin VI gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:16235133 1557473 Myo6 myosin VI gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:17329413 1557473 Myo6 myosin VI gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:7493015 1557473 Myo6 myosin VI gene MP:0001394 circling IAGP N RGD:5509061 20191205 MGI PMID:28832620 1557473 Myo6 myosin VI gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:20923982 1557473 Myo6 myosin VI gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20180621 MGI PMID:20224170 1557473 Myo6 myosin VI gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17329413 1557473 Myo6 myosin VI gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:7493015 1557473 Myo6 myosin VI gene MP:0001399 hyperactivity IAGP N RGD:5509061 20191205 MGI PMID:28832620 1557473 Myo6 myosin VI gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200618 MGI PMID:31103816 1557473 Myo6 myosin VI gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200618 MGI PMID:31103816 1557473 Myo6 myosin VI gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:7493015 1557473 Myo6 myosin VI gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:15978262 1557473 Myo6 myosin VI gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200514 MGI 1557473 Myo6 myosin VI gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17329413 1557473 Myo6 myosin VI gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:16235133 1557473 Myo6 myosin VI gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:17329413 1557473 Myo6 myosin VI gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:10900098 1557473 Myo6 myosin VI gene MP:0001525 impaired balance IAGP N RGD:5509061 20180621 MGI PMID:20224170 1557473 Myo6 myosin VI gene MP:0001525 impaired balance IAGP N RGD:5509061 20200618 MGI PMID:31103816 1557473 Myo6 myosin VI gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:10900098 1557473 Myo6 myosin VI gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220519 MGI 1557473 Myo6 myosin VI gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:7493015 1557473 Myo6 myosin VI gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:16235133 1557473 Myo6 myosin VI gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0001967 deafness IAGP N RGD:5509061 20160929 MGI PMID:27534441 1557473 Myo6 myosin VI gene MP:0001967 deafness IAGP N RGD:5509061 20200618 MGI PMID:31103816 1557473 Myo6 myosin VI gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220519 MGI 1557473 Myo6 myosin VI gene MP:0002730 head shaking IEA N RGD:5509061 20111116 MGI 1557473 Myo6 myosin VI gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20180621 MGI PMID:20224170 1557473 Myo6 myosin VI gene MP:0002895 abnormal otolithic membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 1557473 Myo6 myosin VI gene MP:0003150 detached tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7493015 1557473 Myo6 myosin VI gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200514 MGI 1557473 Myo6 myosin VI gene MP:0004298 vestibular ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10900098 1557473 Myo6 myosin VI gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0004328 decreased vestibular hair cell number IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0004331 vestibular saccular macula degeneration IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0004334 utricular macular degeneration IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10900098 1557473 Myo6 myosin VI gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:7493015 1557473 Myo6 myosin VI gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20180621 MGI PMID:20224170 1557473 Myo6 myosin VI gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20200618 MGI PMID:31103816 1557473 Myo6 myosin VI gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10900098 1557473 Myo6 myosin VI gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:7493015 1557473 Myo6 myosin VI gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20180621 MGI PMID:20224170 1557473 Myo6 myosin VI gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10900098 1557473 Myo6 myosin VI gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:7493015 1557473 Myo6 myosin VI gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20180621 MGI PMID:20224170 1557473 Myo6 myosin VI gene MP:0004409 abnormal crista ampullaris neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0004416 absent cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:7493015 1557473 Myo6 myosin VI gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20180621 MGI PMID:20224170 1557473 Myo6 myosin VI gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20191205 MGI PMID:28832620 1557473 Myo6 myosin VI gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20200618 MGI PMID:31103816 1557473 Myo6 myosin VI gene MP:0004516 fused vestibular hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:10900098 1557473 Myo6 myosin VI gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:12966030 1557473 Myo6 myosin VI gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:17329413 1557473 Myo6 myosin VI gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20180621 MGI PMID:20224170 1557473 Myo6 myosin VI gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20191205 MGI PMID:28832620 1557473 Myo6 myosin VI gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20200618 MGI PMID:31103816 1557473 Myo6 myosin VI gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20191205 MGI PMID:28832620 1557473 Myo6 myosin VI gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20200618 MGI PMID:31103816 1557473 Myo6 myosin VI gene MP:0004523 decreased cochlear hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:17329413 1557473 Myo6 myosin VI gene MP:0004523 decreased cochlear hair cell stereocilia number IAGP N RGD:5509061 20191205 MGI PMID:28832620 1557473 Myo6 myosin VI gene MP:0004524 short cochlear hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:12966030 1557473 Myo6 myosin VI gene MP:0004528 fused outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:10525338 1557473 Myo6 myosin VI gene MP:0004528 fused outer hair cell stereocilia IAGP N RGD:5509061 20180621 MGI PMID:20224170 1557473 Myo6 myosin VI gene MP:0004528 fused outer hair cell stereocilia IAGP N RGD:5509061 20191205 MGI PMID:28832620 1557473 Myo6 myosin VI gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20180621 MGI PMID:20224170 1557473 Myo6 myosin VI gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20191205 MGI PMID:28832620 1557473 Myo6 myosin VI gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20200618 MGI PMID:31103816 1557473 Myo6 myosin VI gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:10525338 1557473 Myo6 myosin VI gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20180621 MGI PMID:20224170 1557473 Myo6 myosin VI gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20191205 MGI PMID:28832620 1557473 Myo6 myosin VI gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20200618 MGI PMID:31103816 1557473 Myo6 myosin VI gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0004589 abnormal cochlear hair cell development IAGP N RGD:5509061 20141003 MGI PMID:10900098 1557473 Myo6 myosin VI gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1557473 Myo6 myosin VI gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12966030 1557473 Myo6 myosin VI gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 1557473 Myo6 myosin VI gene MP:0004814 reduced linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 1557473 Myo6 myosin VI gene MP:0004924 abnormal behavior IEA N RGD:5509061 20200514 MGI 1557473 Myo6 myosin VI gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:20923982 1557473 Myo6 myosin VI gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:10900098 1557473 Myo6 myosin VI gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:7493015 1557473 Myo6 myosin VI gene MP:0005307 head tossing IAGP N RGD:5509061 20180621 MGI PMID:20224170 1557473 Myo6 myosin VI gene MP:0005307 head tossing IAGP N RGD:5509061 20200618 MGI PMID:31103816 1557473 Myo6 myosin VI gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210128 MGI 1557473 Myo6 myosin VI gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15978262 1557473 Myo6 myosin VI gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20220519 MGI 1557473 Myo6 myosin VI gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0006325 impaired hearing IAGP N RGD:5509061 20191205 MGI PMID:28832620 1557473 Myo6 myosin VI gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:10900098 1557473 Myo6 myosin VI gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20180621 MGI PMID:20224170 1557473 Myo6 myosin VI gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220519 MGI 1557473 Myo6 myosin VI gene MP:0010015 abnormal cuticular plate morphology IAGP N RGD:5509061 20191205 MGI PMID:28832620 1557473 Myo6 myosin VI gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200514 MGI 1557473 Myo6 myosin VI gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1557473 Myo6 myosin VI gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200514 MGI 1557473 Myo6 myosin VI gene MP:0010323 retropulsion IAGP N RGD:5509061 20141003 MGI PMID:10900098 1557473 Myo6 myosin VI gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210128 MGI 1557473 Myo6 myosin VI gene MP:0011060 abnormal kinocilium morphology IAGP N RGD:5509061 20191205 MGI PMID:28832620 1557473 Myo6 myosin VI gene MP:0011062 abnormal outer hair cell kinocilium morphology IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:5980120 1557473 Myo6 myosin VI gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1557473 Myo6 myosin VI gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20191205 MGI PMID:28832620 1557473 Myo6 myosin VI gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17329413 1557473 Myo6 myosin VI gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23485424 1557473 Myo6 myosin VI gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20180621 MGI PMID:20224170 1557473 Myo6 myosin VI gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200618 MGI PMID:31103816 1557473 Myo6 myosin VI gene MP:0020084 short ears IEA N RGD:5509061 20170914 MGI 1557474 Zdhhc24 zinc finger, DHHC domain containing 24 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1557474 Zdhhc24 zinc finger, DHHC domain containing 24 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1557475 Hecw2 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20210722 MGI PMID:25555806 1557475 Hecw2 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210722 MGI PMID:25555806 1557475 Hecw2 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210722 MGI PMID:25555806 1557475 Hecw2 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 gene MP:0009854 impaired gastric peristalsis IAGP N RGD:5509061 20210722 MGI PMID:25555806 1557475 Hecw2 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 gene MP:0010801 abnormal myenteric nerve plexus morphology IAGP N RGD:5509061 20210722 MGI PMID:25555806 1557475 Hecw2 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210722 MGI PMID:25555806 1557475 Hecw2 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557475 Hecw2 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 gene MP:0013958 decreased small intestine length IAGP N RGD:5509061 20210722 MGI PMID:25555806 1557475 Hecw2 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20210722 MGI PMID:25555806 1557476 Plcb2 phospholipase C, beta 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1557476 Plcb2 phospholipase C, beta 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1557476 Plcb2 phospholipase C, beta 2 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:10669417 1557476 Plcb2 phospholipase C, beta 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1557476 Plcb2 phospholipase C, beta 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1557476 Plcb2 phospholipase C, beta 2 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1557476 Plcb2 phospholipase C, beta 2 gene MP:0001985 abnormal gustatory system physiology IAGP N RGD:5509061 20141003 MGI PMID:12581520 1557476 Plcb2 phospholipase C, beta 2 gene MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12581520 1557476 Plcb2 phospholipase C, beta 2 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20160623 MGI PMID:26046438 1557476 Plcb2 phospholipase C, beta 2 gene MP:0002409 decreased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:9223297 1557476 Plcb2 phospholipase C, beta 2 gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20141003 MGI PMID:9223297 1557476 Plcb2 phospholipase C, beta 2 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9223297 1557476 Plcb2 phospholipase C, beta 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:9223297 1557476 Plcb2 phospholipase C, beta 2 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:10669417 1557476 Plcb2 phospholipase C, beta 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:10669417 1557476 Plcb2 phospholipase C, beta 2 gene MP:0004209 abnormal sweet taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12581520 1557476 Plcb2 phospholipase C, beta 2 gene MP:0004210 abnormal bitter taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12581520 1557476 Plcb2 phospholipase C, beta 2 gene MP:0004867 decreased platelet calcium level IAGP N RGD:5509061 20141003 MGI PMID:10669417 1557476 Plcb2 phospholipase C, beta 2 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:10669417 1557476 Plcb2 phospholipase C, beta 2 gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 1557476 Plcb2 phospholipase C, beta 2 gene MP:0009449 increased platelet ATP level IAGP N RGD:5509061 20141003 MGI PMID:10669417 1557476 Plcb2 phospholipase C, beta 2 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:10669417 1557476 Plcb2 phospholipase C, beta 2 gene MP:0011678 abnormal vomeronasal sensory neuron physiology IAGP N RGD:5509061 20160623 MGI PMID:26046438 1557476 Plcb2 phospholipase C, beta 2 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201002 MGI PMID:10669417 1557479 Zzef1 zinc finger, ZZ-type with EF hand domain 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1557479 Zzef1 zinc finger, ZZ-type with EF hand domain 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20240523 MGI 1557479 Zzef1 zinc finger, ZZ-type with EF hand domain 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20210520 MGI 1557479 Zzef1 zinc finger, ZZ-type with EF hand domain 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1557479 Zzef1 zinc finger, ZZ-type with EF hand domain 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1557479 Zzef1 zinc finger, ZZ-type with EF hand domain 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1557479 Zzef1 zinc finger, ZZ-type with EF hand domain 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1557479 Zzef1 zinc finger, ZZ-type with EF hand domain 1 gene MP:0003063 increased coping response IEA N RGD:5509061 20210826 MGI 1557479 Zzef1 zinc finger, ZZ-type with EF hand domain 1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20210128 MGI 1557479 Zzef1 zinc finger, ZZ-type with EF hand domain 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1557479 Zzef1 zinc finger, ZZ-type with EF hand domain 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1557479 Zzef1 zinc finger, ZZ-type with EF hand domain 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1557479 Zzef1 zinc finger, ZZ-type with EF hand domain 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20240523 MGI 1557479 Zzef1 zinc finger, ZZ-type with EF hand domain 1 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20160421 MGI 1557479 Zzef1 zinc finger, ZZ-type with EF hand domain 1 gene MP:0030610 absent teeth IEA N RGD:5509061 20240523 MGI 1557480 Lrrn1 leucine rich repeat protein 1, neuronal gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20141003 MGI 1557480 Lrrn1 leucine rich repeat protein 1, neuronal gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20141003 MGI 1557480 Lrrn1 leucine rich repeat protein 1, neuronal gene MP:0003169 abnormal scala media morphology IAGP N RGD:5509061 20240229 MGI PMID:37369584 1557480 Lrrn1 leucine rich repeat protein 1, neuronal gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20240229 MGI PMID:37369584 1557480 Lrrn1 leucine rich repeat protein 1, neuronal gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20240229 MGI PMID:37369584 1557481 Actrt3 actin related protein T3 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20181227 MGI 1557481 Actrt3 actin related protein T3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1557481 Actrt3 actin related protein T3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 1557484 Zbed5 zinc finger BED-type containing 5 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20230601 MGI 1557486 Osbpl3 oxysterol binding protein-like 3 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20160114 MGI 1557486 Osbpl3 oxysterol binding protein-like 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1557486 Osbpl3 oxysterol binding protein-like 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1557486 Osbpl3 oxysterol binding protein-like 3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20200402 MGI 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0000751 myopathy IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0001314 cornea opacity IEA N RGD:5509061 20210826 MGI 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0010014 hippocampus pyramidal cell degeneration IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557489 Gmppa GDP-mannose pyrophosphorylase A gene MP:0020240 increased skeletal muscle cell apoptosis IAGP N RGD:5509061 20210603 MGI PMID:33755596 1557490 Mknk1 MAP kinase-interacting serine/threonine kinase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15254222 1557495 Hyal6 hyaluronoglucosaminidase 6 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1557495 Hyal6 hyaluronoglucosaminidase 6 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220811 MGI 1557496 Thsd7b thrombospondin, type I, domain containing 7B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1557497 Megf11 multiple EGF-like-domains 11 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22407321 1557497 Megf11 multiple EGF-like-domains 11 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22407321 1557498 Stoml1 stomatin-like 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1557498 Stoml1 stomatin-like 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1557498 Stoml1 stomatin-like 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1557498 Stoml1 stomatin-like 1 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20220519 MGI 1557498 Stoml1 stomatin-like 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1557498 Stoml1 stomatin-like 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220519 MGI 1557498 Stoml1 stomatin-like 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20151001 MGI PMID:24247984 1557498 Stoml1 stomatin-like 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20210128 MGI 1557498 Stoml1 stomatin-like 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20210128 MGI 1557500 H1f8 H1.8 linker histone gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1557500 H1f8 H1.8 linker histone gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1557500 H1f8 H1.8 linker histone gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 1557500 H1f8 H1.8 linker histone gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0001263 weight loss IAGP N RGD:5509061 20210121 MGI PMID:32876667 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0002083 premature death IAGP N RGD:5509061 20210121 MGI PMID:32876667 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0004969 pale kidney IAGP N RGD:5509061 20210121 MGI PMID:32876667 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011352 proximal convoluted tubule brush border loss IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011359 decreased glomerular capillary number IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12858174 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011454 abnormal glomerular endothelium fenestra morphology IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011498 abnormal glomerular capsule parietal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557502 Rrm2b ribonucleotide reductase M2 B (TP53 inducible) gene MP:0011871 podocyte hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15723268 1557504 Lrrcc1 leucine rich repeat and coiled-coil domain containing 1 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20210805 MGI 1557504 Lrrcc1 leucine rich repeat and coiled-coil domain containing 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1557504 Lrrcc1 leucine rich repeat and coiled-coil domain containing 1 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210805 MGI 1557504 Lrrcc1 leucine rich repeat and coiled-coil domain containing 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20231207 MGI 1557505 Atoh8 atonal bHLH transcription factor 8 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18560595 1557505 Atoh8 atonal bHLH transcription factor 8 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23836893 1557506 Washc5 WASH complex subunit 5 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1557506 Washc5 WASH complex subunit 5 gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20171116 MGI PMID:27390154 1557506 Washc5 WASH complex subunit 5 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 1557506 Washc5 WASH complex subunit 5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20181129 MGI PMID:26572744 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20190418 MGI PMID:29950491 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20190418 MGI PMID:29950491 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0000536 hydroureter IAGP N RGD:5509061 20190418 MGI PMID:29950491 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20190418 MGI PMID:29950491 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20230803 MGI PMID:36727488 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0001257 increased body length IEA N RGD:5509061 20220811 MGI 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0001914 hemorrhage IEA N RGD:5509061 20221215 MGI 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20230803 MGI PMID:36727488 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20190418 MGI PMID:29950491 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20221215 MGI 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20190418 MGI PMID:29950491 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20190418 MGI PMID:29950491 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20230803 MGI PMID:36727488 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20190418 MGI PMID:29950491 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1557512 Dis3l2 DIS3 like 3'-5' exoribonuclease 2 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20230803 MGI PMID:36727488 1557514 Zmym6 zinc finger, MYM-type 6 gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20211021 MGI 1557515 Plekha8 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 8 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1557515 Plekha8 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 8 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1557515 Plekha8 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 8 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1557515 Plekha8 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 8 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170105 MGI 1557515 Plekha8 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 8 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20170105 MGI 1557515 Plekha8 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 8 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210128 MGI 1557516 Tbc1d25 TBC1 domain family, member 25 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20201105 MGI PMID:32210723 1557516 Tbc1d25 TBC1 domain family, member 25 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 1557516 Tbc1d25 TBC1 domain family, member 25 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20201105 MGI PMID:32210723 1557516 Tbc1d25 TBC1 domain family, member 25 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20201105 MGI PMID:32210723 1557516 Tbc1d25 TBC1 domain family, member 25 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20201105 MGI PMID:32210723 1557516 Tbc1d25 TBC1 domain family, member 25 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20201105 MGI PMID:32210723 1557516 Tbc1d25 TBC1 domain family, member 25 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20201105 MGI PMID:32210723 1557516 Tbc1d25 TBC1 domain family, member 25 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20201105 MGI PMID:32210723 1557516 Tbc1d25 TBC1 domain family, member 25 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20201105 MGI PMID:32210723 1557516 Tbc1d25 TBC1 domain family, member 25 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20201105 MGI PMID:32210723 1557516 Tbc1d25 TBC1 domain family, member 25 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20201105 MGI PMID:32210723 1557516 Tbc1d25 TBC1 domain family, member 25 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0000751 myopathy IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20181227 MGI 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20190228 MGI PMID:29905857 1557517 Gfpt1 glutamine fructose-6-phosphate transaminase 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1557519 Tfe3 transcription factor E3 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:11930005 1557519 Tfe3 transcription factor E3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11930005 1557519 Tfe3 transcription factor E3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11930005 1557519 Tfe3 transcription factor E3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11930005 1557519 Tfe3 transcription factor E3 gene MP:0003053 delayed tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:11930005 1557519 Tfe3 transcription factor E3 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:11930005 1557519 Tfe3 transcription factor E3 gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11930005 1557519 Tfe3 transcription factor E3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11930005 1557519 Tfe3 transcription factor E3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11930005 1557520 Aldh16a1 aldehyde dehydrogenase 16 family, member A1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1557520 Aldh16a1 aldehyde dehydrogenase 16 family, member A1 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20190221 MGI PMID:28254523 1557520 Aldh16a1 aldehyde dehydrogenase 16 family, member A1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20190221 MGI PMID:28254523 1557520 Aldh16a1 aldehyde dehydrogenase 16 family, member A1 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20141003 MGI 1557520 Aldh16a1 aldehyde dehydrogenase 16 family, member A1 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20141003 MGI 1557521 Ifi204 interferon activated gene 204 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1557521 Ifi204 interferon activated gene 204 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20190912 MGI PMID:29472103 1557521 Ifi204 interferon activated gene 204 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20190912 MGI PMID:29472103 1557521 Ifi204 interferon activated gene 204 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20190912 MGI PMID:29472103 1557521 Ifi204 interferon activated gene 204 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20190912 MGI PMID:29472103 1557521 Ifi204 interferon activated gene 204 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20190912 MGI PMID:29472103 1557521 Ifi204 interferon activated gene 204 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20190912 MGI PMID:29472103 1557521 Ifi204 interferon activated gene 204 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20190912 MGI PMID:29472103 1557521 Ifi204 interferon activated gene 204 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20190912 MGI PMID:29472103 1557522 Ccny cyclin Y gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0001399 hyperactivity IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0009303 decreased renal fat pad weight IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20151008 MGI PMID:26305884 1557522 Ccny cyclin Y gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557522 Ccny cyclin Y gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20151008 MGI PMID:26161966 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0000433 microcephaly IEA N RGD:5509061 20231207 MGI 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0000562 polydactyly IEA N RGD:5509061 20231207 MGI 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0000564 syndactyly IEA N RGD:5509061 20231207 MGI 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:9883721 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9883721 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20160331 MGI PMID:24441682 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20231207 MGI 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20231207 MGI 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160331 MGI PMID:24441682 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200220 MGI PMID:31680851 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:9883721 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20200220 MGI PMID:31680851 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20160331 MGI PMID:24441682 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20231207 MGI 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:21285371 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20160331 MGI PMID:24441682 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20200220 MGI PMID:31680851 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20200220 MGI PMID:31680851 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:9883721 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20160331 MGI PMID:24441682 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0002969 impaired social transmission of food preference IAGP N RGD:5509061 20160331 MGI PMID:24441682 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0003054 spina bifida IEA N RGD:5509061 20231207 MGI 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20200220 MGI PMID:31680851 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20160331 MGI PMID:24441682 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0005237 abnormal olfactory tract morphology IAGP N RGD:5509061 20141003 MGI PMID:9883721 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0005267 abnormal olfactory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9883721 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20231207 MGI 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20231207 MGI 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20160331 MGI PMID:24441682 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0009941 abnormal olfactory bulb interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9883721 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0009947 abnormal olfactory bulb external plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9883721 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9883721 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0009951 abnormal olfactory bulb mitral cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9883721 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0009954 abnormal mitral cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9883721 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0009955 abnormal olfactory bulb tufted cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9883721 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0010059 olfactory bulb hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9883721 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9883721 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200220 MGI PMID:31680851 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20200220 MGI PMID:31680851 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0014115 cognitive inflexibility IAGP N RGD:5509061 20160331 MGI PMID:24441682 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0014378 increased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:31680851 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:31680851 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:24441682 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0020870 decreased thigmotaxis IAGP N RGD:5509061 20200220 MGI PMID:31680851 1557526 Tbr1 T-box brain transcription factor 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:31680851 1557530 Brsk1 BR serine/threonine kinase 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15705853 1557530 Brsk1 BR serine/threonine kinase 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15705853 1557530 Brsk1 BR serine/threonine kinase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15705853 1557530 Brsk1 BR serine/threonine kinase 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15705853 1557530 Brsk1 BR serine/threonine kinase 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:15705853 1557530 Brsk1 BR serine/threonine kinase 1 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:15705853 1557530 Brsk1 BR serine/threonine kinase 1 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:15705853 1557530 Brsk1 BR serine/threonine kinase 1 gene MP:0008440 abnormal subplate morphology IAGP N RGD:5509061 20141003 MGI PMID:15705853 1557530 Brsk1 BR serine/threonine kinase 1 gene MP:0008442 disorganized cortical plate IAGP N RGD:5509061 20141003 MGI PMID:15705853 1557530 Brsk1 BR serine/threonine kinase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15705853 1557530 Brsk1 BR serine/threonine kinase 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:15705853 1557530 Brsk1 BR serine/threonine kinase 1 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:15705853 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20221215 MGI 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0000692 small spleen IEA N RGD:5509061 20220519 MGI 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220519 MGI 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20220811 MGI PMID:34096614 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220811 MGI PMID:34096614 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20220519 MGI 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20220811 MGI PMID:34096614 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220811 MGI PMID:34096614 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220811 MGI PMID:34096614 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0003883 enlarged stomach IEA N RGD:5509061 20220519 MGI 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220811 MGI PMID:34096614 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220811 MGI PMID:34096614 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20190207 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220811 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0031373 abnormal manchette perinuclear ring morphology IAGP N RGD:5509061 20220407 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0031375 abnormal manchette disassembly IAGP N RGD:5509061 20220407 MGI PMID:29136647 1557532 Katnal2 katanin p60 subunit A-like 2 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20220428 MGI PMID:29136647 1557534 Cdx4 caudal type homeobox 4 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557534 Cdx4 caudal type homeobox 4 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557534 Cdx4 caudal type homeobox 4 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557534 Cdx4 caudal type homeobox 4 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557534 Cdx4 caudal type homeobox 4 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557534 Cdx4 caudal type homeobox 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557534 Cdx4 caudal type homeobox 4 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557534 Cdx4 caudal type homeobox 4 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557534 Cdx4 caudal type homeobox 4 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557534 Cdx4 caudal type homeobox 4 gene MP:0003445 sirenomelia IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557534 Cdx4 caudal type homeobox 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557534 Cdx4 caudal type homeobox 4 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:18511567 1557534 Cdx4 caudal type homeobox 4 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557534 Cdx4 caudal type homeobox 4 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557534 Cdx4 caudal type homeobox 4 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557534 Cdx4 caudal type homeobox 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557534 Cdx4 caudal type homeobox 4 gene MP:0012127 absent placenta hemotrichorial membrane IAGP N RGD:5509061 20141003 MGI PMID:16396910 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19020030 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19625617 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19020030 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19020030 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0001746 abnormal pituitary secretion IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:19625617 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0003506 acromegaly IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0003838 abnormal milk ejection IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19020030 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:19020030 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:19020030 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19020030 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:19625617 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0008779 abnormal maternal behavior IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19625617 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:19625617 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19020030 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19625617 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19625617 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0012010 parturition failure IAGP N RGD:5509061 20141003 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:19625617 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:19020030 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0030567 abnormal I band morphology IAGP N RGD:5509061 20180531 MGI PMID:23116210 1557535 Kalrn kalirin, RhoGEF kinase gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:19625617 1557537 Med12 mediator complex subunit 12 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:20589884 1557537 Med12 mediator complex subunit 12 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20589884 1557537 Med12 mediator complex subunit 12 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20589884 1557537 Med12 mediator complex subunit 12 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:20589884 1557537 Med12 mediator complex subunit 12 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20141003 MGI PMID:20589884 1557537 Med12 mediator complex subunit 12 gene MP:0004603 absent vertebral arch IAGP N RGD:5509061 20141003 MGI PMID:20589884 1557537 Med12 mediator complex subunit 12 gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:20589884 1557537 Med12 mediator complex subunit 12 gene MP:0010642 absent third pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20589884 1557537 Med12 mediator complex subunit 12 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20589884 1557537 Med12 mediator complex subunit 12 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557537 Med12 mediator complex subunit 12 gene MP:0012159 absent anterior visceral endoderm IAGP N RGD:5509061 20141003 MGI PMID:20630950 1557538 Lipn lipase, family member N gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170105 MGI 1557539 Casz1 castor zinc finger 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20221215 MGI 1557539 Casz1 castor zinc finger 1 gene MP:0001633 poor circulation IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0001785 edema IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0003900 shortened QT interval IEA N RGD:5509061 20230601 MGI 1557539 Casz1 castor zinc finger 1 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0004062 dilated heart right atrium IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0008727 increased heart right atrium size IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0010200 enlarged lymphatic vessel IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0010500 myocardium hypoplasia IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0010640 ventricular myocardium compact layer hypoplasia IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557539 Casz1 castor zinc finger 1 gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0012269 nuchal edema IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0012515 abnormal heart apex morphology IAGP N RGD:5509061 20161229 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0013848 subcutaneous edema IAGP N RGD:5509061 20170803 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:25190801 1557539 Casz1 castor zinc finger 1 gene MP:0031611 decreased fetal cardiomyocyte number IAGP N RGD:5509061 20240321 MGI PMID:25953344 1557539 Casz1 castor zinc finger 1 gene MP:0031613 fetal cardiomyocyte disarray IAGP N RGD:5509061 20240321 MGI PMID:25190801 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0008956 decreased cellular hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20141003 MGI PMID:9927493 1557540 Epb41 erythrocyte membrane protein band 4.1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557542 Usp17lc ubiquitin specific peptidase 17-like C gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22984479 1557542 Usp17lc ubiquitin specific peptidase 17-like C gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22984479 1557542 Usp17lc ubiquitin specific peptidase 17-like C gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22984479 1557542 Usp17lc ubiquitin specific peptidase 17-like C gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:22984479 1557542 Usp17lc ubiquitin specific peptidase 17-like C gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22984479 1557542 Usp17lc ubiquitin specific peptidase 17-like C gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:22984479 1557542 Usp17lc ubiquitin specific peptidase 17-like C gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22984479 1557542 Usp17lc ubiquitin specific peptidase 17-like C gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22984479 1557542 Usp17lc ubiquitin specific peptidase 17-like C gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22984479 1557542 Usp17lc ubiquitin specific peptidase 17-like C gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22984479 1557542 Usp17lc ubiquitin specific peptidase 17-like C gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22984479 1557542 Usp17lc ubiquitin specific peptidase 17-like C gene MP:0012119 increased trophectoderm apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22984479 1557542 Usp17lc ubiquitin specific peptidase 17-like C gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:22984479 1557544 Nod1 nucleotide-binding oligomerization domain containing 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:16418393 1557544 Nod1 nucleotide-binding oligomerization domain containing 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18261938 1557544 Nod1 nucleotide-binding oligomerization domain containing 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16418393 1557544 Nod1 nucleotide-binding oligomerization domain containing 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18261938 1557544 Nod1 nucleotide-binding oligomerization domain containing 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16418393 1557544 Nod1 nucleotide-binding oligomerization domain containing 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18261938 1557544 Nod1 nucleotide-binding oligomerization domain containing 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:18261938 1557544 Nod1 nucleotide-binding oligomerization domain containing 1 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16418393 1557546 Lats1 large tumor suppressor gene MP:0000599 enlarged liver IAGP N RGD:5509061 20150910 MGI PMID:26109051 1557546 Lats1 large tumor suppressor gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23230145 1557546 Lats1 large tumor suppressor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1557546 Lats1 large tumor suppressor gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23230145 1557546 Lats1 large tumor suppressor gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1557546 Lats1 large tumor suppressor gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1557546 Lats1 large tumor suppressor gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1557546 Lats1 large tumor suppressor gene MP:0002981 increased liver weight IAGP N RGD:5509061 20150910 MGI PMID:26109051 1557546 Lats1 large tumor suppressor gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:23230145 1557546 Lats1 large tumor suppressor gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:23230145 1557546 Lats1 large tumor suppressor gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23230145 1557546 Lats1 large tumor suppressor gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1557546 Lats1 large tumor suppressor gene MP:0009733 absent nipple IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:23230145 1557546 Lats1 large tumor suppressor gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1557546 Lats1 large tumor suppressor gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200514 MGI 1557546 Lats1 large tumor suppressor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23230145 1557546 Lats1 large tumor suppressor gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:23230145 1557546 Lats1 large tumor suppressor gene MP:0013348 adenohypophysis hyperplasia IAGP N RGD:5509061 20150129 MGI PMID:9988269 1557546 Lats1 large tumor suppressor gene MP:0013611 abnormal bile duct epithelium morphology IAGP N RGD:5509061 20150910 MGI PMID:26109051 1557546 Lats1 large tumor suppressor gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:23230145 1557547 Gnpnat1 glucosamine-phosphate N-acetyltransferase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11013212 1557547 Gnpnat1 glucosamine-phosphate N-acetyltransferase 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:11013212 1557547 Gnpnat1 glucosamine-phosphate N-acetyltransferase 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11013212 1557547 Gnpnat1 glucosamine-phosphate N-acetyltransferase 1 gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:11013212 1557547 Gnpnat1 glucosamine-phosphate N-acetyltransferase 1 gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:11013212 1557547 Gnpnat1 glucosamine-phosphate N-acetyltransferase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11013212 1557547 Gnpnat1 glucosamine-phosphate N-acetyltransferase 1 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:11013212 1557547 Gnpnat1 glucosamine-phosphate N-acetyltransferase 1 gene MP:0009593 absent chorion IAGP N RGD:5509061 20141003 MGI PMID:11013212 1557547 Gnpnat1 glucosamine-phosphate N-acetyltransferase 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11013212 1557548 Mrtfb myocardin related transcription factor B gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17183527 1557548 Mrtfb myocardin related transcription factor B gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20191003 MGI PMID:31147515 1557548 Mrtfb myocardin related transcription factor B gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15951419 1557548 Mrtfb myocardin related transcription factor B gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:16204380 1557548 Mrtfb myocardin related transcription factor B gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17183527 1557548 Mrtfb myocardin related transcription factor B gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22899851 1557548 Mrtfb myocardin related transcription factor B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22899851 1557548 Mrtfb myocardin related transcription factor B gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:17183527 1557548 Mrtfb myocardin related transcription factor B gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:17183527 1557548 Mrtfb myocardin related transcription factor B gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15951419 1557548 Mrtfb myocardin related transcription factor B gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:16204380 1557548 Mrtfb myocardin related transcription factor B gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16204380 1557548 Mrtfb myocardin related transcription factor B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:22899851 1557548 Mrtfb myocardin related transcription factor B gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15951419 1557548 Mrtfb myocardin related transcription factor B gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:17183527 1557548 Mrtfb myocardin related transcription factor B gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:16204380 1557548 Mrtfb myocardin related transcription factor B gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:17183527 1557548 Mrtfb myocardin related transcription factor B gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15951419 1557548 Mrtfb myocardin related transcription factor B gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16204380 1557548 Mrtfb myocardin related transcription factor B gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0003279 aneurysm IAGP N RGD:5509061 20141003 MGI PMID:22899851 1557548 Mrtfb myocardin related transcription factor B gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:22899851 1557548 Mrtfb myocardin related transcription factor B gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16204380 1557548 Mrtfb myocardin related transcription factor B gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17183527 1557548 Mrtfb myocardin related transcription factor B gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22899851 1557548 Mrtfb myocardin related transcription factor B gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20191003 MGI PMID:31147515 1557548 Mrtfb myocardin related transcription factor B gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15951419 1557548 Mrtfb myocardin related transcription factor B gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15951419 1557548 Mrtfb myocardin related transcription factor B gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20191003 MGI PMID:31147515 1557548 Mrtfb myocardin related transcription factor B gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20191003 MGI PMID:31147515 1557548 Mrtfb myocardin related transcription factor B gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:22899851 1557548 Mrtfb myocardin related transcription factor B gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:15951419 1557548 Mrtfb myocardin related transcription factor B gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:22899851 1557548 Mrtfb myocardin related transcription factor B gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16204380 1557548 Mrtfb myocardin related transcription factor B gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16204380 1557548 Mrtfb myocardin related transcription factor B gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0009868 abnormal descending thoracic aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:22899851 1557548 Mrtfb myocardin related transcription factor B gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:22899851 1557548 Mrtfb myocardin related transcription factor B gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15951419 1557548 Mrtfb myocardin related transcription factor B gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17183527 1557548 Mrtfb myocardin related transcription factor B gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16204380 1557548 Mrtfb myocardin related transcription factor B gene MP:0010425 abnormal heart and great vessel attachment IAGP N RGD:5509061 20141003 MGI PMID:16204380 1557548 Mrtfb myocardin related transcription factor B gene MP:0010574 dilated aorta IAGP N RGD:5509061 20141003 MGI PMID:22899851 1557548 Mrtfb myocardin related transcription factor B gene MP:0010652 absent aorticopulmonary septum IAGP N RGD:5509061 20141003 MGI PMID:15951419 1557548 Mrtfb myocardin related transcription factor B gene MP:0010666 abnormal vitelline vein morphology IAGP N RGD:5509061 20150521 MGI PMID:17183527 1557548 Mrtfb myocardin related transcription factor B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15951419 1557548 Mrtfb myocardin related transcription factor B gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16204380 1557548 Mrtfb myocardin related transcription factor B gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22899851 1557548 Mrtfb myocardin related transcription factor B gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17183527 1557548 Mrtfb myocardin related transcription factor B gene MP:0011707 impaired fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:20534669 1557548 Mrtfb myocardin related transcription factor B gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:22899851 1557548 Mrtfb myocardin related transcription factor B gene MP:0012751 impaired cardiac neural crest cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15951419 1557548 Mrtfb myocardin related transcription factor B gene MP:0013187 dilated basilar artery IAGP N RGD:5509061 20141003 MGI PMID:22899851 1557548 Mrtfb myocardin related transcription factor B gene MP:0030338 dilated third pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:22899851 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20221020 MGI PMID:34732852 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20221020 MGI PMID:34732852 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20240523 MGI 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:34732852 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0001575 cyanosis IAGP N RGD:5509061 20221020 MGI PMID:34732852 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20221020 MGI PMID:34732852 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0003109 short femur IAGP N RGD:5509061 20221020 MGI PMID:34732852 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20221020 MGI PMID:34732852 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0004351 short humerus IAGP N RGD:5509061 20221020 MGI PMID:34732852 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0004911 absent mandibular condyloid process IAGP N RGD:5509061 20221020 MGI PMID:34732852 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0005352 small cranium IAGP N RGD:5509061 20221020 MGI PMID:34732852 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20221020 MGI PMID:34732852 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221020 MGI PMID:34732852 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221020 MGI PMID:34732852 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:34732852 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1557549 Zfhx4 zinc finger homeodomain 4 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:34732852 1557550 Tbx15 T-box 15 gene MP:0000023 abnormal ear position IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0000023 abnormal ear position IAGP N RGD:5509061 20141003 MGI PMID:15728667 1557550 Tbx15 T-box 15 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:14737183 1557550 Tbx15 T-box 15 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15728667 1557550 Tbx15 T-box 15 gene MP:0000088 short mandible IAGP N RGD:5509061 20171214 MGI PMID:15728667 1557550 Tbx15 T-box 15 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:15728667 1557550 Tbx15 T-box 15 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:13654621 1557550 Tbx15 T-box 15 gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:14737183 1557550 Tbx15 T-box 15 gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:14737183 1557550 Tbx15 T-box 15 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:14737183 1557550 Tbx15 T-box 15 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:13654621 1557550 Tbx15 T-box 15 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:14737183 1557550 Tbx15 T-box 15 gene MP:0000449 broad nasal bridge IAGP N RGD:5509061 20141003 MGI PMID:13654621 1557550 Tbx15 T-box 15 gene MP:0000449 broad nasal bridge IAGP N RGD:5509061 20141003 MGI PMID:14737183 1557550 Tbx15 T-box 15 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14737183 1557550 Tbx15 T-box 15 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:14737183 1557550 Tbx15 T-box 15 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:13654621 1557550 Tbx15 T-box 15 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:14737183 1557550 Tbx15 T-box 15 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:13654621 1557550 Tbx15 T-box 15 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:13654621 1557550 Tbx15 T-box 15 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004338 small clavicle IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004339 absent clavicle IAGP N RGD:5509061 20141003 MGI PMID:15728667 1557550 Tbx15 T-box 15 gene MP:0004342 scapular bone foramen IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004342 scapular bone foramen IAGP N RGD:5509061 20141003 MGI PMID:15728667 1557550 Tbx15 T-box 15 gene MP:0004343 small scapula IAGP N RGD:5509061 20141003 MGI PMID:13654621 1557550 Tbx15 T-box 15 gene MP:0004343 small scapula IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004343 small scapula IAGP N RGD:5509061 20141003 MGI PMID:15728667 1557550 Tbx15 T-box 15 gene MP:0004345 abnormal acromion morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004347 abnormal scapular spine morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004347 abnormal scapular spine morphology IAGP N RGD:5509061 20141003 MGI PMID:15728667 1557550 Tbx15 T-box 15 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004447 small basioccipital bone IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004508 abnormal pectoral girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15728667 1557550 Tbx15 T-box 15 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20171214 MGI PMID:15728667 1557550 Tbx15 T-box 15 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15728667 1557550 Tbx15 T-box 15 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:15728667 1557550 Tbx15 T-box 15 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004635 short metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004659 abnormal odontoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0004659 abnormal odontoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:15728667 1557550 Tbx15 T-box 15 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141225 MGI PMID:14737183 1557550 Tbx15 T-box 15 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:14737183 1557550 Tbx15 T-box 15 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0008154 decreased diameter of humerus IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0008237 abnormal ventral coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:14737183 1557550 Tbx15 T-box 15 gene MP:0008238 abnormal dorsoventral coat patterning IAGP N RGD:5509061 20141003 MGI PMID:14737183 1557550 Tbx15 T-box 15 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:15728667 1557550 Tbx15 T-box 15 gene MP:0008526 decreased cranium width IAGP N RGD:5509061 20141003 MGI PMID:15728667 1557550 Tbx15 T-box 15 gene MP:0010941 abnormal foramen magnum morphology IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:13654621 1557550 Tbx15 T-box 15 gene MP:0030189 broad snout IAGP N RGD:5509061 20171019 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0030833 small acromion IAGP N RGD:5509061 20181018 MGI PMID:13654621 1557550 Tbx15 T-box 15 gene MP:0030833 small acromion IAGP N RGD:5509061 20181018 MGI PMID:15652702 1557550 Tbx15 T-box 15 gene MP:0030833 small acromion IAGP N RGD:5509061 20181018 MGI PMID:15728667 1557551 Cyth4 cytohesin 4 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20240523 MGI 1557551 Cyth4 cytohesin 4 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1557551 Cyth4 cytohesin 4 gene MP:0006415 absent testes IEA N RGD:5509061 20240523 MGI 1557551 Cyth4 cytohesin 4 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20240523 MGI 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20151126 MGI PMID:24626990 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0000066 osteoporosis IAGP N RGD:5509061 20151126 MGI PMID:24626990 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0000111 cleft palate IEA N RGD:5509061 20150827 MGI 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20151126 MGI PMID:24626990 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0000642 enlarged adrenal glands IEA N RGD:5509061 20150827 MGI 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:12242664 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20151126 MGI PMID:24626990 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20150827 MGI 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:12242664 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11280729 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9789047 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10757812 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20151126 MGI PMID:24626990 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0002925 abnormal cardiovascular development IEA N RGD:5509061 20150827 MGI 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20151126 MGI PMID:24626990 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0003820 increased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:12242664 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20151126 MGI PMID:24626990 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10757812 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20151126 MGI PMID:24626990 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20151126 MGI PMID:24626990 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:11280729 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0010484 bicuspid aortic valve IEA N RGD:5509061 20150827 MGI 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0010527 bicuspid pulmonary valve IEA N RGD:5509061 20150827 MGI 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20151126 MGI PMID:24626990 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20151126 MGI PMID:24626990 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:15235603 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20151126 MGI PMID:24626990 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0010924 abnormal osteoid morphology IAGP N RGD:5509061 20151126 MGI PMID:24626990 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20151126 MGI PMID:24626990 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9789047 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20151126 MGI PMID:24626990 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0014427 increased circulating hyaluronic acid level IAGP N RGD:5509061 20240425 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20170202 MGI PMID:16330174 1557552 Wrn Werner syndrome RecQ like helicase gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:15235603 1557555 Cntrl centriolin gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1557555 Cntrl centriolin gene MP:0000519 hydronephrosis IEA N RGD:5509061 20141003 MGI 1557555 Cntrl centriolin gene MP:0000536 hydroureter IEA N RGD:5509061 20151203 MGI 1557555 Cntrl centriolin gene MP:0001297 microphthalmia IEA N RGD:5509061 20151203 MGI 1557555 Cntrl centriolin gene MP:0003675 kidney cyst IEA N RGD:5509061 20141003 MGI 1557555 Cntrl centriolin gene MP:0004200 decreased fetal size IEA N RGD:5509061 20151203 MGI 1557555 Cntrl centriolin gene MP:0004860 dilated kidney collecting duct IEA N RGD:5509061 20151203 MGI 1557555 Cntrl centriolin gene MP:0006124 tricuspid valve stenosis IEA N RGD:5509061 20141003 MGI 1557555 Cntrl centriolin gene MP:0008528 polycystic kidney IEA N RGD:5509061 20151203 MGI 1557555 Cntrl centriolin gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141003 MGI 1557555 Cntrl centriolin gene MP:0010403 atrial septal defect IEA N RGD:5509061 20141003 MGI 1557555 Cntrl centriolin gene MP:0010422 heart right ventricle hypoplasia IEA N RGD:5509061 20141003 MGI 1557555 Cntrl centriolin gene MP:0010457 pulmonary artery stenosis IEA N RGD:5509061 20151203 MGI 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200625 MGI PMID:26015500 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0000578 ulcerated autopod IAGP N RGD:5509061 20141003 MGI PMID:18806225 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20200625 MGI PMID:26015500 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:22649252 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:21239721 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20200625 MGI PMID:26015500 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:20855887 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0002297 abnormal forced expiratory flow rates IAGP N RGD:5509061 20200625 MGI PMID:26015500 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20200625 MGI PMID:26015500 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21760953 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12935356 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15322195 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17312165 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12855817 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12872135 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:21760953 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12855817 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:12855817 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16714379 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20855887 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22649252 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:17190817 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17312165 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17082622 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17190817 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:18178804 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:18423196 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22796522 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20200625 MGI PMID:26015500 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:20505141 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18981228 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21760953 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18178804 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200625 MGI PMID:26015500 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:21760953 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008524 increased plasmacytoid dendritic cell number IAGP N RGD:5509061 20200625 MGI PMID:26015500 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20855887 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008552 abnormal circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:18713975 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:12935356 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17312165 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008557 abnormal interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:21998457 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:12872135 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22550345 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20200625 MGI PMID:26015500 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:18178804 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18423196 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008648 decreased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:18178804 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20855887 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:17312165 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:21239721 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:21760953 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:17312165 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20200625 MGI PMID:26015500 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12855817 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12872135 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:16625202 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:16625202 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20855887 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12855817 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:18802464 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0010750 increased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17082622 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21760953 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0011077 decreased macrophage nitric oxide production IAGP N RGD:5509061 20141003 MGI PMID:12872135 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0011077 decreased macrophage nitric oxide production IAGP N RGD:5509061 20141003 MGI PMID:17082622 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20141003 MGI PMID:12872135 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20141003 MGI PMID:17082622 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20141003 MGI PMID:17312165 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0011081 decreased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12872135 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0011081 decreased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15322195 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0013022 increased Ly6C high monocyte number IAGP N RGD:5509061 20200625 MGI PMID:26015500 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0013026 decreased Ly6C low monocyte number IAGP N RGD:5509061 20200625 MGI PMID:26015500 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20150219 MGI PMID:24557836 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:12872135 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0020927 abnormal susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:18802464 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:21239721 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:21998457 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0020947 decreased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:18423196 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200625 MGI PMID:26015500 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0031040 increased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:21239721 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0031040 increased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:21998457 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200625 MGI PMID:26015500 1557557 Ticam1 TIR domain containing adaptor molecule 1 gene MP:0031266 decreased susceptibility to alcohol-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:18713975 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20171207 MGI PMID:28263186 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0002083 premature death IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20171207 MGI PMID:28263186 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0003717 pallor IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20171207 MGI PMID:28263186 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0011261 abnormal limb mesenchyme morphology IAGP N RGD:5509061 20171207 MGI PMID:28263186 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0012556 increased cell death IAGP N RGD:5509061 20170601 MGI PMID:26544067 1557559 Ddrgk1 DDRGK domain containing 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20171207 MGI PMID:28263186 1557562 Tbx3 T-box 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:22130515 1557562 Tbx3 T-box 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:17460765 1557562 Tbx3 T-box 3 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:22130515 1557562 Tbx3 T-box 3 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0000555 absent carpal bone IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0000555 absent carpal bone IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:17473172 1557562 Tbx3 T-box 3 gene MP:0000629 absent mammary gland IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1557562 Tbx3 T-box 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1557562 Tbx3 T-box 3 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0001142 abnormal vagina orifice morphology IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17460765 1557562 Tbx3 T-box 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230119 MGI 1557562 Tbx3 T-box 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1557562 Tbx3 T-box 3 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0001679 thin apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:17460765 1557562 Tbx3 T-box 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1557562 Tbx3 T-box 3 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:17473172 1557562 Tbx3 T-box 3 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19769959 1557562 Tbx3 T-box 3 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230119 MGI 1557562 Tbx3 T-box 3 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20231207 MGI 1557562 Tbx3 T-box 3 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1557562 Tbx3 T-box 3 gene MP:0003074 absent metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0003127 abnormal clitoris morphology IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17460765 1557562 Tbx3 T-box 3 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0003898 abnormal QRS complex IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0003928 increased heart rate variability IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22130515 1557562 Tbx3 T-box 3 gene MP:0004070 abnormal P wave IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0004115 abnormal sinoatrial node morphology IAGP N RGD:5509061 20141003 MGI PMID:17473172 1557562 Tbx3 T-box 3 gene MP:0004122 abnormal sinus arrhythmia IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0004135 abnormal mammary gland embryonic development IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:17460765 1557562 Tbx3 T-box 3 gene MP:0004360 absent ulna IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0004576 abnormal embryonic autopod plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0005430 absent fibula IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0006063 abnormal inferior vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:17460765 1557562 Tbx3 T-box 3 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20231207 MGI 1557562 Tbx3 T-box 3 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0009328 delayed heart looping IAGP N RGD:5509061 20141003 MGI PMID:17460765 1557562 Tbx3 T-box 3 gene MP:0009382 abnormal cardiac jelly morphology IAGP N RGD:5509061 20141003 MGI PMID:22130515 1557562 Tbx3 T-box 3 gene MP:0009729 absent tarsus bones IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:19769959 1557562 Tbx3 T-box 3 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:19769959 1557562 Tbx3 T-box 3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1557562 Tbx3 T-box 3 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0010510 absent P wave IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0010511 shortened PR interval IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0010512 absent PR interval IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17473172 1557562 Tbx3 T-box 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19769959 1557562 Tbx3 T-box 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19769959 1557562 Tbx3 T-box 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22203979 1557562 Tbx3 T-box 3 gene MP:0013169 small hindlimb buds IAGP N RGD:5509061 20141003 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230119 MGI 1557562 Tbx3 T-box 3 gene MP:0013785 abnormal mammary gland bud morphology IAGP N RGD:5509061 20150611 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:17460765 1557562 Tbx3 T-box 3 gene MP:0020515 abnormal visceral yolk sac endoderm morphology IAGP N RGD:5509061 20180125 MGI PMID:12668638 1557562 Tbx3 T-box 3 gene MP:0031541 decreased sinoatrial node size IAGP N RGD:5509061 20240104 MGI PMID:17473172 1557562 Tbx3 T-box 3 gene MP:0031542 sinoatrial node hypoplasia IAGP N RGD:5509061 20240104 MGI PMID:22203979 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17442300 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17442300 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17442300 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0000272 abnormal aorta morphology IEA N RGD:5509061 20141003 MGI 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20141003 MGI 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15755804 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17442300 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9636176 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17442300 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20141003 MGI PMID:17442300 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20181227 MGI 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17442300 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:17442300 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0002746 abnormal semilunar valve morphology IEA N RGD:5509061 20141003 MGI 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0002748 abnormal pulmonary valve morphology IEA N RGD:5509061 20141003 MGI 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:17442300 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0004383 absent interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:17442300 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0004838 abnormal neural fold elevation formation IAGP N RGD:5509061 20141003 MGI PMID:17442300 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:9636176 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20141003 MGI 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20141003 MGI 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0010469 ascending aorta hypoplasia IEA N RGD:5509061 20141003 MGI 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0010476 coronary fistula IEA N RGD:5509061 20141003 MGI 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0010541 aorta hypoplasia IEA N RGD:5509061 20141003 MGI 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:17442300 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0030028 absent exoccipital bone IAGP N RGD:5509061 20170810 MGI PMID:17442300 1557564 Hectd1 HECT domain E3 ubiquitin protein ligase 1 gene MP:0030329 absent temporal bone petrous part IAGP N RGD:5509061 20171109 MGI PMID:17442300 1557565 Arhgef38 Rho guanine nucleotide exchange factor 38 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20181227 MGI 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20201022 MGI 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:9482885 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0001128 ovary hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9482885 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9482885 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9482885 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9482885 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9482885 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9482885 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20181227 MGI 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:9482885 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20201022 MGI 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:9482885 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9482885 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10921895 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10921895 1557567 Tial1 Tia1 cytotoxic granule-associated RNA binding protein-like 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9482885 1557569 Pax7 paired box 7 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:8631261 1557569 Pax7 paired box 7 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23410975 1557569 Pax7 paired box 7 gene MP:0000448 pointed snout IAGP N RGD:5509061 20141003 MGI PMID:8631261 1557569 Pax7 paired box 7 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15520281 1557569 Pax7 paired box 7 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:8631261 1557569 Pax7 paired box 7 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:19554048 1557569 Pax7 paired box 7 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:17418413 1557569 Pax7 paired box 7 gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15520281 1557569 Pax7 paired box 7 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:15843801 1557569 Pax7 paired box 7 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:11030621 1557569 Pax7 paired box 7 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:11030621 1557569 Pax7 paired box 7 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:15282552 1557569 Pax7 paired box 7 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:19554048 1557569 Pax7 paired box 7 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:21828093 1557569 Pax7 paired box 7 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:22945933 1557569 Pax7 paired box 7 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:23933088 1557569 Pax7 paired box 7 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:23410975 1557569 Pax7 paired box 7 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23933088 1557569 Pax7 paired box 7 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:11030621 1557569 Pax7 paired box 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15520281 1557569 Pax7 paired box 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22869749 1557569 Pax7 paired box 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23933088 1557569 Pax7 paired box 7 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19213072 1557569 Pax7 paired box 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11030621 1557569 Pax7 paired box 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15520281 1557569 Pax7 paired box 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8631261 1557569 Pax7 paired box 7 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24239359 1557569 Pax7 paired box 7 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24239359 1557569 Pax7 paired box 7 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20170420 MGI PMID:26987019 1557569 Pax7 paired box 7 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20170420 MGI PMID:26987019 1557569 Pax7 paired box 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15520281 1557569 Pax7 paired box 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21828093 1557569 Pax7 paired box 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8631261 1557569 Pax7 paired box 7 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:22945933 1557569 Pax7 paired box 7 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20190704 MGI PMID:26854227 1557569 Pax7 paired box 7 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23933088 1557569 Pax7 paired box 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15520281 1557569 Pax7 paired box 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19332644 1557569 Pax7 paired box 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180322 MGI PMID:29415061 1557569 Pax7 paired box 7 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:15520281 1557569 Pax7 paired box 7 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1557569 Pax7 paired box 7 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:15520281 1557569 Pax7 paired box 7 gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:15282552 1557569 Pax7 paired box 7 gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:15520281 1557569 Pax7 paired box 7 gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:21828091 1557569 Pax7 paired box 7 gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:21828093 1557569 Pax7 paired box 7 gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:23933088 1557569 Pax7 paired box 7 gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:23933088 1557569 Pax7 paired box 7 gene MP:0004477 turbinate hypoplasia IAGP N RGD:5509061 20170921 MGI PMID:15520281 1557569 Pax7 paired box 7 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:21828093 1557569 Pax7 paired box 7 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:8631261 1557569 Pax7 paired box 7 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:15520281 1557569 Pax7 paired box 7 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:21828093 1557569 Pax7 paired box 7 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:22869749 1557569 Pax7 paired box 7 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20190704 MGI PMID:26854227 1557569 Pax7 paired box 7 gene MP:0005247 abnormal extraocular muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19531352 1557569 Pax7 paired box 7 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20211209 MGI PMID:33753492 1557569 Pax7 paired box 7 gene MP:0006039 decreased mitochondrial fission IAGP N RGD:5509061 20211209 MGI PMID:33753492 1557569 Pax7 paired box 7 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19213072 1557569 Pax7 paired box 7 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20190704 MGI PMID:26854227 1557569 Pax7 paired box 7 gene MP:0008052 abnormal serous gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8631261 1557569 Pax7 paired box 7 gene MP:0009398 abnormal skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:22869749 1557569 Pax7 paired box 7 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:11030621 1557569 Pax7 paired box 7 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:15520281 1557569 Pax7 paired box 7 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:23933088 1557569 Pax7 paired box 7 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:23933088 1557569 Pax7 paired box 7 gene MP:0009407 increased skeletal muscle fiber density IAGP N RGD:5509061 20141003 MGI PMID:15520281 1557569 Pax7 paired box 7 gene MP:0009410 abnormal skeletal muscle satellite cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23933088 1557569 Pax7 paired box 7 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19554048 1557569 Pax7 paired box 7 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21828091 1557569 Pax7 paired box 7 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22945933 1557569 Pax7 paired box 7 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23933088 1557569 Pax7 paired box 7 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:21828093 1557569 Pax7 paired box 7 gene MP:0010238 increased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:22869749 1557569 Pax7 paired box 7 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:22869749 1557569 Pax7 paired box 7 gene MP:0010240 decreased skeletal muscle size IAGP N RGD:5509061 20141003 MGI PMID:23933088 1557569 Pax7 paired box 7 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20211209 MGI PMID:33753492 1557569 Pax7 paired box 7 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20211209 MGI PMID:33753492 1557569 Pax7 paired box 7 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20211209 MGI PMID:33753492 1557569 Pax7 paired box 7 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22869749 1557569 Pax7 paired box 7 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8631261 1557569 Pax7 paired box 7 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15843801 1557569 Pax7 paired box 7 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20211209 MGI PMID:33753492 1557569 Pax7 paired box 7 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17418413 1557569 Pax7 paired box 7 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23410975 1557569 Pax7 paired box 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557569 Pax7 paired box 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557569 Pax7 paired box 7 gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20201217 MGI PMID:31685980 1557569 Pax7 paired box 7 gene MP:0012185 abnormal muscle precursor cell morphology IAGP N RGD:5509061 20160721 MGI PMID:26999603 1557569 Pax7 paired box 7 gene MP:0012185 abnormal muscle precursor cell morphology IAGP N RGD:5509061 20210513 MGI PMID:32094117 1557569 Pax7 paired box 7 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:22279050 1557569 Pax7 paired box 7 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:23933088 1557569 Pax7 paired box 7 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20160721 MGI PMID:26999603 1557569 Pax7 paired box 7 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20190704 MGI PMID:26854227 1557569 Pax7 paired box 7 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20201217 MGI PMID:31685980 1557569 Pax7 paired box 7 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:19554048 1557569 Pax7 paired box 7 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:21828091 1557569 Pax7 paired box 7 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:21828093 1557569 Pax7 paired box 7 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211209 MGI PMID:33753492 1557569 Pax7 paired box 7 gene MP:0030056 lacrimal bone hypoplasia IAGP N RGD:5509061 20170921 MGI PMID:15520281 1557569 Pax7 paired box 7 gene MP:0031328 delayed skeletal muscle regeneration IAGP N RGD:5509061 20220106 MGI PMID:32483152 1557571 Slc39a1 solute carrier family 39 (zinc transporter), member 1 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:16652366 1557571 Slc39a1 solute carrier family 39 (zinc transporter), member 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:16652366 1557571 Slc39a1 solute carrier family 39 (zinc transporter), member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151203 MGI PMID:16652366 1557571 Slc39a1 solute carrier family 39 (zinc transporter), member 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:16652366 1557571 Slc39a1 solute carrier family 39 (zinc transporter), member 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16652366 1557571 Slc39a1 solute carrier family 39 (zinc transporter), member 1 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:16652366 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:7600574 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7600574 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11454988 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:7600574 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:7670466 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:7670466 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7600574 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:7600574 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:7600574 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:7670466 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7670466 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:7600574 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:7670466 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:7600574 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:7670466 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7670466 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8706124 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:7600574 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7600574 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7670466 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7600574 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7670466 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:7600574 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:7600574 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12594290 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:12594290 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12213735 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:23770692 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20141003 MGI PMID:12213735 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20141003 MGI PMID:12594290 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20141003 MGI PMID:7600574 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:7670466 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12213735 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12213735 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23770692 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:23770692 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20141003 MGI PMID:23770692 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0012507 midbrain atrophy IAGP N RGD:5509061 20141003 MGI PMID:7670466 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:7670466 1557572 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal gene MP:0031058 hepatosplenomegaly IAGP N RGD:5509061 20200618 MGI PMID:7600574 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:23630012 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:23630012 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23630012 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:23630012 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:23630012 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:23630012 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:23630012 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:23630012 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:23630012 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0010011 ectopic hippocampus pyramidal cells IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:23630012 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:23630012 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23630012 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0011150 abnormal hippocampus stratum oriens morphology IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557573 Pik3r4 phosphoinositide-3-kinase regulatory subunit 4 gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557574 Irak1 interleukin-1 receptor-associated kinase 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12860565 1557574 Irak1 interleukin-1 receptor-associated kinase 1 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:12860565 1557574 Irak1 interleukin-1 receptor-associated kinase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22007846 1557574 Irak1 interleukin-1 receptor-associated kinase 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18438411 1557574 Irak1 interleukin-1 receptor-associated kinase 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18438411 1557574 Irak1 interleukin-1 receptor-associated kinase 1 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:12860565 1557574 Irak1 interleukin-1 receptor-associated kinase 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12626533 1557574 Irak1 interleukin-1 receptor-associated kinase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9625767 1557574 Irak1 interleukin-1 receptor-associated kinase 1 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:23918981 1557574 Irak1 interleukin-1 receptor-associated kinase 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:18438411 1557574 Irak1 interleukin-1 receptor-associated kinase 1 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1557578 Trex2 three prime repair exonuclease 2 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19654293 1557578 Trex2 three prime repair exonuclease 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:19654293 1557578 Trex2 three prime repair exonuclease 2 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:19654293 1557578 Trex2 three prime repair exonuclease 2 gene MP:0009581 decreased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19654293 1557579 Fgfbp3 fibroblast growth factor binding protein 3 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 1557579 Fgfbp3 fibroblast growth factor binding protein 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20851768 1557581 Krt18 keratin 18 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20220609 MGI PMID:27689336 1557581 Krt18 keratin 18 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:9508776 1557581 Krt18 keratin 18 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20220609 MGI PMID:27689336 1557581 Krt18 keratin 18 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20220609 MGI PMID:27689336 1557581 Krt18 keratin 18 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11013209 1557581 Krt18 keratin 18 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20220609 MGI PMID:27689336 1557581 Krt18 keratin 18 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11013209 1557581 Krt18 keratin 18 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20220609 MGI PMID:27689336 1557581 Krt18 keratin 18 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20220609 MGI PMID:27689336 1557581 Krt18 keratin 18 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20220609 MGI PMID:27689336 1557581 Krt18 keratin 18 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20220609 MGI PMID:27689336 1557581 Krt18 keratin 18 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:11013209 1557581 Krt18 keratin 18 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11013209 1557581 Krt18 keratin 18 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20220609 MGI PMID:27689336 1557581 Krt18 keratin 18 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20220609 MGI PMID:27689336 1557581 Krt18 keratin 18 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20220609 MGI PMID:27689336 1557581 Krt18 keratin 18 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11013209 1557581 Krt18 keratin 18 gene MP:0014045 Mallory bodies IAGP N RGD:5509061 20220609 MGI PMID:27689336 1557582 Tatdn3 TatD DNase domain containing 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20170105 MGI 1557582 Tatdn3 TatD DNase domain containing 3 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1557582 Tatdn3 TatD DNase domain containing 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 1557584 Tbx22 T-box 22 gene MP:0000098 abnormal vomer bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19648291 1557584 Tbx22 T-box 22 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20240523 MGI 1557584 Tbx22 T-box 22 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1557584 Tbx22 T-box 22 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:19648291 1557584 Tbx22 T-box 22 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19648291 1557584 Tbx22 T-box 22 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:19648291 1557584 Tbx22 T-box 22 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1557584 Tbx22 T-box 22 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19648291 1557584 Tbx22 T-box 22 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:19648291 1557584 Tbx22 T-box 22 gene MP:0008970 choanal atresia IAGP N RGD:5509061 20141003 MGI PMID:19648291 1557584 Tbx22 T-box 22 gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20141003 MGI PMID:19648291 1557584 Tbx22 T-box 22 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:19648291 1557584 Tbx22 T-box 22 gene MP:0009892 palate bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19648291 1557584 Tbx22 T-box 22 gene MP:0009895 decreased palatine bone horizontal plate size IAGP N RGD:5509061 20141003 MGI PMID:19648291 1557584 Tbx22 T-box 22 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19648291 1557584 Tbx22 T-box 22 gene MP:0013264 tongue ankylosis IAGP N RGD:5509061 20141003 MGI PMID:19648291 1557584 Tbx22 T-box 22 gene MP:0030183 persistent oronasal membrane IAGP N RGD:5509061 20171012 MGI PMID:19648291 1557584 Tbx22 T-box 22 gene MP:0030266 small vomer bone IAGP N RGD:5509061 20171026 MGI PMID:19648291 1557585 Cad carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase gene MP:0001263 weight loss IAGP N RGD:5509061 20191128 MGI PMID:29551634 1557585 Cad carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase gene MP:0001513 limb grasping IEA N RGD:5509061 20201022 MGI 1557585 Cad carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20191128 MGI PMID:29551634 1557585 Cad carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1557585 Cad carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557585 Cad carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1557586 Naaa N-acylethanolamine acid amidase gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1557586 Naaa N-acylethanolamine acid amidase gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1557586 Naaa N-acylethanolamine acid amidase gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1557586 Naaa N-acylethanolamine acid amidase gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1557588 Tenm1 teneurin transmembrane protein 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230119 MGI 1557588 Tenm1 teneurin transmembrane protein 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230119 MGI 1557588 Tenm1 teneurin transmembrane protein 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1557588 Tenm1 teneurin transmembrane protein 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230119 MGI 1557588 Tenm1 teneurin transmembrane protein 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1557588 Tenm1 teneurin transmembrane protein 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1557590 Eda ectodysplasin-A gene MP:0000116 abnormal tooth development IEA N RGD:5509061 20120209 MGI 1557590 Eda ectodysplasin-A gene MP:0000119 abnormal tooth eruption IEA N RGD:5509061 20111116 MGI 1557590 Eda ectodysplasin-A gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:18689798 1557590 Eda ectodysplasin-A gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:5959976 1557590 Eda ectodysplasin-A gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:18689798 1557590 Eda ectodysplasin-A gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:2055107 1557590 Eda ectodysplasin-A gene MP:0000396 increased curvature of hairs IEA N RGD:5509061 20111116 MGI 1557590 Eda ectodysplasin-A gene MP:0000397 abnormal guard hair morphology IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20141003 MGI PMID:18689798 1557590 Eda ectodysplasin-A gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:18689798 1557590 Eda ectodysplasin-A gene MP:0000416 sparse hair IEA N RGD:5509061 20111116 MGI 1557590 Eda ectodysplasin-A gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:5893447 1557590 Eda ectodysplasin-A gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:18689798 1557590 Eda ectodysplasin-A gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:2055107 1557590 Eda ectodysplasin-A gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:2055107 1557590 Eda ectodysplasin-A gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:2055107 1557590 Eda ectodysplasin-A gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:2348861 1557590 Eda ectodysplasin-A gene MP:0000577 absent eccrine glands IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0000577 absent eccrine glands IAGP N RGD:5509061 20141003 MGI PMID:2348861 1557590 Eda ectodysplasin-A gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:5893447 1557590 Eda ectodysplasin-A gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:2055107 1557590 Eda ectodysplasin-A gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0001218 thin epidermis IAGP N RGD:5509061 20181101 MGI PMID:7544943 1557590 Eda ectodysplasin-A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:2055107 1557590 Eda ectodysplasin-A gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0001302 eyelids open at birth IEA N RGD:5509061 20120209 MGI 1557590 Eda ectodysplasin-A gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:15972955 1557590 Eda ectodysplasin-A gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:15972955 1557590 Eda ectodysplasin-A gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:15972955 1557590 Eda ectodysplasin-A gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:15972955 1557590 Eda ectodysplasin-A gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:15972955 1557590 Eda ectodysplasin-A gene MP:0001926 female infertility IEA N RGD:5509061 20141003 MGI 1557590 Eda ectodysplasin-A gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:15972955 1557590 Eda ectodysplasin-A gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10932191 1557590 Eda ectodysplasin-A gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:2055107 1557590 Eda ectodysplasin-A gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:15972955 1557590 Eda ectodysplasin-A gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:18689798 1557590 Eda ectodysplasin-A gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20170314 MGI 1557590 Eda ectodysplasin-A gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0002163 abnormal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0002277 abnormal respiratory mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:15973734 1557590 Eda ectodysplasin-A gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:5893447 1557590 Eda ectodysplasin-A gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:5893447 1557590 Eda ectodysplasin-A gene MP:0002717 abnormal male preputial gland morphology IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:2055107 1557590 Eda ectodysplasin-A gene MP:0002832 coarse hair IEA N RGD:5509061 20111116 MGI 1557590 Eda ectodysplasin-A gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:18689798 1557590 Eda ectodysplasin-A gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20181101 MGI PMID:7544943 1557590 Eda ectodysplasin-A gene MP:0003815 hairless IEA N RGD:5509061 20120209 MGI 1557590 Eda ectodysplasin-A gene MP:0003932 abnormal molar crown morphology IAGP N RGD:5509061 20180125 MGI PMID:478295 1557590 Eda ectodysplasin-A gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0004830 short incisors IAGP N RGD:5509061 20141003 MGI PMID:5959976 1557590 Eda ectodysplasin-A gene MP:0005176 eyelids fail to open IEA N RGD:5509061 20120209 MGI 1557590 Eda ectodysplasin-A gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:15972955 1557590 Eda ectodysplasin-A gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:15972955 1557590 Eda ectodysplasin-A gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:5893447 1557590 Eda ectodysplasin-A gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:5959976 1557590 Eda ectodysplasin-A gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:15972955 1557590 Eda ectodysplasin-A gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15972955 1557590 Eda ectodysplasin-A gene MP:0006236 absent Meibomian glands IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0006236 absent Meibomian glands IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0006236 absent Meibomian glands IAGP N RGD:5509061 20141003 MGI PMID:15972955 1557590 Eda ectodysplasin-A gene MP:0006363 absent auchene hairs IAGP N RGD:5509061 20141003 MGI PMID:18689798 1557590 Eda ectodysplasin-A gene MP:0006365 absent guard hair IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0006365 absent guard hair IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0006365 absent guard hair IAGP N RGD:5509061 20141003 MGI PMID:18689798 1557590 Eda ectodysplasin-A gene MP:0006365 absent guard hair IAGP N RGD:5509061 20141003 MGI PMID:5893447 1557590 Eda ectodysplasin-A gene MP:0006366 absent zigzag hairs IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0006366 absent zigzag hairs IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0006366 absent zigzag hairs IAGP N RGD:5509061 20141003 MGI PMID:18689798 1557590 Eda ectodysplasin-A gene MP:0006366 absent zigzag hairs IAGP N RGD:5509061 20141003 MGI PMID:5893447 1557590 Eda ectodysplasin-A gene MP:0006367 absent sweat gland IAGP N RGD:5509061 20141003 MGI PMID:18689798 1557590 Eda ectodysplasin-A gene MP:0006369 supernumerary incisors IAGP N RGD:5509061 20141003 MGI PMID:2055107 1557590 Eda ectodysplasin-A gene MP:0006370 abnormal hair follicle pheomelanosome pheomelanin content IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0006371 absent hair follicle pheomelanosome pheomelanin IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0006400 decreased molar number IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0006400 decreased molar number IAGP N RGD:5509061 20141003 MGI PMID:18689798 1557590 Eda ectodysplasin-A gene MP:0006400 decreased molar number IAGP N RGD:5509061 20141003 MGI PMID:5893447 1557590 Eda ectodysplasin-A gene MP:0006400 decreased molar number IAGP N RGD:5509061 20141003 MGI PMID:5959976 1557590 Eda ectodysplasin-A gene MP:0006401 absent male preputial gland IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0006402 small molars IAGP N RGD:5509061 20141003 MGI PMID:478295 1557590 Eda ectodysplasin-A gene MP:0006402 small molars IAGP N RGD:5509061 20141003 MGI PMID:5959976 1557590 Eda ectodysplasin-A gene MP:0008538 decreased zigzag hair amount IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0009003 abnormal vibrissa number IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20141003 MGI PMID:18028050 1557590 Eda ectodysplasin-A gene MP:0009659 striated fur IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0009659 striated fur IAGP N RGD:5509061 20141003 MGI PMID:2055107 1557590 Eda ectodysplasin-A gene MP:0009793 sebaceous gland hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15972955 1557590 Eda ectodysplasin-A gene MP:0009794 sebaceous gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0010031 abnormal cranium size IAGP N RGD:5509061 20141003 MGI PMID:2055107 1557590 Eda ectodysplasin-A gene MP:0010231 transverse fur striping IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0010231 transverse fur striping IAGP N RGD:5509061 20141003 MGI PMID:2055107 1557590 Eda ectodysplasin-A gene MP:0010233 hairless tail IAGP N RGD:5509061 20141003 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2055107 1557590 Eda ectodysplasin-A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20150618 MGI PMID:2055107 1557590 Eda ectodysplasin-A gene MP:0012078 abnormal tail ring morphology IAGP N RGD:5509061 20170309 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0013177 abnormal tail tip morphology IAGP N RGD:5509061 20141225 MGI PMID:13103353 1557590 Eda ectodysplasin-A gene MP:0013370 anhidrosis IAGP N RGD:5509061 20141225 MGI PMID:18689798 1557590 Eda ectodysplasin-A gene MP:0013370 anhidrosis IAGP N RGD:5509061 20141225 MGI PMID:2348861 1557590 Eda ectodysplasin-A gene MP:0013373 increased sebum secretion IAGP N RGD:5509061 20141218 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0013378 increased sebocyte number IAGP N RGD:5509061 20141218 MGI PMID:14506134 1557590 Eda ectodysplasin-A gene MP:0013478 corneal limbitis IAGP N RGD:5509061 20150205 MGI PMID:15972955 1557590 Eda ectodysplasin-A gene MP:0013558 abnormal exocrine gland morphology IEA N RGD:5509061 20150702 MGI 1557590 Eda ectodysplasin-A gene MP:0013580 abnormal nasal gland morphology IAGP N RGD:5509061 20170119 MGI PMID:27590203 1557590 Eda ectodysplasin-A gene MP:0013582 abnormal lateral nasal gland morphology IAGP N RGD:5509061 20170119 MGI PMID:27590203 1557590 Eda ectodysplasin-A gene MP:0013745 abnormal eyelid margin morphology IAGP N RGD:5509061 20150416 MGI PMID:15972955 1557590 Eda ectodysplasin-A gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20171221 MGI PMID:5893447 1557590 Eda ectodysplasin-A gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20180125 MGI PMID:18689798 1557590 Eda ectodysplasin-A gene MP:0030494 abnormal molar root morphology IAGP N RGD:5509061 20180125 MGI PMID:5893447 1557592 Cdh12 cadherin 12 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1557593 Map3k11 mitogen-activated protein kinase kinase kinase 11 gene MP:0000116 abnormal tooth development IEA N RGD:5509061 20111116 MGI 1557593 Map3k11 mitogen-activated protein kinase kinase kinase 11 gene MP:0001216 abnormal epidermal layer morphology IEA N RGD:5509061 20111116 MGI 1557593 Map3k11 mitogen-activated protein kinase kinase kinase 11 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:15831472 1557593 Map3k11 mitogen-activated protein kinase kinase kinase 11 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20111116 MGI 1557593 Map3k11 mitogen-activated protein kinase kinase kinase 11 gene MP:0002819 abnormal dental pulp cavity morphology IEA N RGD:5509061 20111116 MGI 1557593 Map3k11 mitogen-activated protein kinase kinase kinase 11 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:21979919 1557593 Map3k11 mitogen-activated protein kinase kinase kinase 11 gene MP:0009931 abnormal skin appearance IEA N RGD:5509061 20111116 MGI 1557593 Map3k11 mitogen-activated protein kinase kinase kinase 11 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:21979919 1557593 Map3k11 mitogen-activated protein kinase kinase kinase 11 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:21979919 1557593 Map3k11 mitogen-activated protein kinase kinase kinase 11 gene MP:0011084 lethality at weaning, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20220804 MGI PMID:35312628 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:15367666 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15367666 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220811 MGI PMID:35312628 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220804 MGI PMID:35312628 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220804 MGI PMID:35312628 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:15367666 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20220811 MGI PMID:35312628 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220804 MGI PMID:35312628 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20220811 MGI PMID:35312628 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220811 MGI PMID:35312628 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15367666 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20220811 MGI PMID:35312628 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15367666 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20220804 MGI PMID:35312628 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20141003 MGI PMID:15367666 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:15367666 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220804 MGI PMID:35312628 1557595 Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220811 MGI PMID:35312628 1557596 Lpar5 lysophosphatidic acid receptor 5 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:23039190 1557596 Lpar5 lysophosphatidic acid receptor 5 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23039190 1557596 Lpar5 lysophosphatidic acid receptor 5 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23039190 1557596 Lpar5 lysophosphatidic acid receptor 5 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:23039190 1557596 Lpar5 lysophosphatidic acid receptor 5 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:23039190 1557596 Lpar5 lysophosphatidic acid receptor 5 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:23039190 1557596 Lpar5 lysophosphatidic acid receptor 5 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:23039190 1557596 Lpar5 lysophosphatidic acid receptor 5 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:23039190 1557596 Lpar5 lysophosphatidic acid receptor 5 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:23039190 1557596 Lpar5 lysophosphatidic acid receptor 5 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:22461625 1557596 Lpar5 lysophosphatidic acid receptor 5 gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20141003 MGI PMID:23039190 1557597 Gpr101 G protein-coupled receptor 101 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1557597 Gpr101 G protein-coupled receptor 101 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1557597 Gpr101 G protein-coupled receptor 101 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1557597 Gpr101 G protein-coupled receptor 101 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20211021 MGI 1557597 Gpr101 G protein-coupled receptor 101 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1557598 Rasa4 RAS p21 protein activator 4 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:16041389 1557598 Rasa4 RAS p21 protein activator 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16041389 1557599 Rcbtb2 regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200618 MGI PMID:26291700 1557599 Rcbtb2 regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200618 MGI PMID:26291700 1557599 Rcbtb2 regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20200618 MGI PMID:26291700 1557599 Rcbtb2 regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2 gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20200618 MGI PMID:26291700 1557599 Rcbtb2 regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20200618 MGI PMID:26291700 1557599 Rcbtb2 regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20200618 MGI PMID:26291700 1557599 Rcbtb2 regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2 gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20200618 MGI PMID:26291700 1557599 Rcbtb2 regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20200618 MGI PMID:26291700 1557599 Rcbtb2 regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20200618 MGI PMID:26291700 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20170921 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20240620 MGI PMID:38671004 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0001785 edema IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0003717 pallor IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20240620 MGI PMID:38671004 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0005352 small cranium IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22869748 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:22869748 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0009579 acephaly IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20240620 MGI PMID:38671004 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240620 MGI PMID:38671004 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22869748 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20150910 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0012240 abnormal hepatoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:14744934 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20240620 MGI PMID:38671004 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0030072 round face IAGP N RGD:5509061 20170921 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:24895408 1557600 Dph1 diphthamide biosynthesis 1 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20221201 MGI PMID:24895408 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0002083 premature death IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0003674 oxidative stress IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0003900 shortened QT interval IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0010393 shortened QRS complex duration IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20210429 MGI PMID:31939735 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1557601 Bud23 BUD23, rRNA methyltransferase and ribosome maturation factor gene MP:0014390 decreased myocardial fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:31939735 1557603 Myl1 myosin, light polypeptide 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16103131 1557603 Myl1 myosin, light polypeptide 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20180927 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20201217 MGI PMID:31530015 1557603 Myl1 myosin, light polypeptide 1 gene MP:0000746 weakness IAGP N RGD:5509061 20180927 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:16103131 1557603 Myl1 myosin, light polypeptide 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16103131 1557603 Myl1 myosin, light polypeptide 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20191219 MGI PMID:24713655 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:12417746 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16103131 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20201217 MGI PMID:31530015 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17626887 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16103131 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180927 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20180927 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:17626887 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20201015 MGI PMID:30989113 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20201015 MGI PMID:30989113 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:11884037 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:11884037 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11884037 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:11884037 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11884037 1557603 Myl1 myosin, light polypeptide 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20201217 MGI PMID:31530015 1557603 Myl1 myosin, light polypeptide 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20201015 MGI PMID:30989113 1557603 Myl1 myosin, light polypeptide 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12417746 1557603 Myl1 myosin, light polypeptide 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16103131 1557603 Myl1 myosin, light polypeptide 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20191107 MGI PMID:28475869 1557603 Myl1 myosin, light polypeptide 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20201015 MGI PMID:30989113 1557603 Myl1 myosin, light polypeptide 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10686620 1557603 Myl1 myosin, light polypeptide 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20201217 MGI PMID:31530015 1557603 Myl1 myosin, light polypeptide 1 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12417746 1557603 Myl1 myosin, light polypeptide 1 gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20190131 MGI PMID:28683291 1557603 Myl1 myosin, light polypeptide 1 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:17626887 1557603 Myl1 myosin, light polypeptide 1 gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:16103131 1557603 Myl1 myosin, light polypeptide 1 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20191219 MGI PMID:24713655 1557603 Myl1 myosin, light polypeptide 1 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:17626887 1557603 Myl1 myosin, light polypeptide 1 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20180927 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:16103131 1557603 Myl1 myosin, light polypeptide 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20180927 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:12417746 1557603 Myl1 myosin, light polypeptide 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20201015 MGI PMID:30989113 1557603 Myl1 myosin, light polypeptide 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20180927 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20201015 MGI PMID:30989113 1557603 Myl1 myosin, light polypeptide 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20191107 MGI PMID:28475869 1557603 Myl1 myosin, light polypeptide 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20191107 MGI PMID:28475869 1557603 Myl1 myosin, light polypeptide 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20191107 MGI PMID:28475869 1557603 Myl1 myosin, light polypeptide 1 gene MP:0008486 decreased muscle spindle number IAGP N RGD:5509061 20141003 MGI PMID:17626887 1557603 Myl1 myosin, light polypeptide 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:11884037 1557603 Myl1 myosin, light polypeptide 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20191219 MGI PMID:24713655 1557603 Myl1 myosin, light polypeptide 1 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:12417746 1557603 Myl1 myosin, light polypeptide 1 gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20191219 MGI PMID:24713655 1557603 Myl1 myosin, light polypeptide 1 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:16103131 1557603 Myl1 myosin, light polypeptide 1 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20180927 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20180927 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20191219 MGI PMID:24713655 1557603 Myl1 myosin, light polypeptide 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20180927 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0010238 increased skeletal muscle weight IAGP N RGD:5509061 20191219 MGI PMID:24713655 1557603 Myl1 myosin, light polypeptide 1 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20180927 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20201217 MGI PMID:31530015 1557603 Myl1 myosin, light polypeptide 1 gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20201217 MGI PMID:31530015 1557603 Myl1 myosin, light polypeptide 1 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20190131 MGI PMID:28683291 1557603 Myl1 myosin, light polypeptide 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20190131 MGI PMID:28683291 1557603 Myl1 myosin, light polypeptide 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:12417746 1557603 Myl1 myosin, light polypeptide 1 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20180927 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20201217 MGI PMID:31530015 1557603 Myl1 myosin, light polypeptide 1 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11884037 1557603 Myl1 myosin, light polypeptide 1 gene MP:0011201 abnormal visceral yolk sac cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:11884037 1557603 Myl1 myosin, light polypeptide 1 gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20180927 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20180927 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20180927 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20201217 MGI PMID:31530015 1557603 Myl1 myosin, light polypeptide 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20190131 MGI PMID:28683291 1557603 Myl1 myosin, light polypeptide 1 gene MP:0012735 abnormal response to exercise IAGP N RGD:5509061 20190131 MGI PMID:28683291 1557603 Myl1 myosin, light polypeptide 1 gene MP:0014342 abnormal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0014389 decreased skeletal muscle fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:29898916 1557603 Myl1 myosin, light polypeptide 1 gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20201015 MGI PMID:30989113 1557603 Myl1 myosin, light polypeptide 1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20191219 MGI PMID:24713655 1557608 Synpo2 synaptopodin 2 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1557608 Synpo2 synaptopodin 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1557608 Synpo2 synaptopodin 2 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1557608 Synpo2 synaptopodin 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1557608 Synpo2 synaptopodin 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1557608 Synpo2 synaptopodin 2 gene MP:0003896 prolonged PR interval IEA N RGD:5509061 20211021 MGI 1557608 Synpo2 synaptopodin 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 1557608 Synpo2 synaptopodin 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557609 Ap1s3 adaptor-related protein complex AP-1, sigma 3 gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20230601 MGI 1557611 Fundc2 FUN14 domain containing 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20210318 MGI PMID:29786068 1557611 Fundc2 FUN14 domain containing 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20210318 MGI PMID:29786068 1557611 Fundc2 FUN14 domain containing 2 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20210318 MGI PMID:30576423 1557612 Rbpms2 RNA binding protein with multiple splicing 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1557612 Rbpms2 RNA binding protein with multiple splicing 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1557612 Rbpms2 RNA binding protein with multiple splicing 2 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1557612 Rbpms2 RNA binding protein with multiple splicing 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1557612 Rbpms2 RNA binding protein with multiple splicing 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20181227 MGI 1557612 Rbpms2 RNA binding protein with multiple splicing 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1557612 Rbpms2 RNA binding protein with multiple splicing 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1557612 Rbpms2 RNA binding protein with multiple splicing 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1557613 Ano5 anoctamin 5 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20180426 MGI PMID:26911675 1557613 Ano5 anoctamin 5 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20180426 MGI PMID:26667038 1557613 Ano5 anoctamin 5 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20180426 MGI PMID:26911675 1557613 Ano5 anoctamin 5 gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20180426 MGI PMID:26911675 1557613 Ano5 anoctamin 5 gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20180426 MGI PMID:26911675 1557613 Ano5 anoctamin 5 gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20180426 MGI PMID:26911675 1557613 Ano5 anoctamin 5 gene MP:0003668 abnormal periodontal ligament morphology IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0005190 osteomyelitis IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180426 MGI PMID:26911675 1557613 Ano5 anoctamin 5 gene MP:0009280 decreased activated sperm motility IAGP N RGD:5509061 20180426 MGI PMID:26667038 1557613 Ano5 anoctamin 5 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20180426 MGI PMID:26911675 1557613 Ano5 anoctamin 5 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20180426 MGI PMID:26911675 1557613 Ano5 anoctamin 5 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20180426 MGI PMID:26911675 1557613 Ano5 anoctamin 5 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0010932 increased trabecular bone connectivity density IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0011642 abnormal bone collagen fibril morphology IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20180426 MGI PMID:26911675 1557613 Ano5 anoctamin 5 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0014344 abnormal skeletal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:26911675 1557613 Ano5 anoctamin 5 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20180426 MGI PMID:26667038 1557613 Ano5 anoctamin 5 gene MP:0030050 large mandible IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0030050 large mandible IAGP N RGD:5509061 20230629 MGI PMID:34841576 1557613 Ano5 anoctamin 5 gene MP:0030132 periodontium inflammation IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0030223 mandibular hyperostosis IAGP N RGD:5509061 20210121 MGI PMID:30712070 1557613 Ano5 anoctamin 5 gene MP:0031328 delayed skeletal muscle regeneration IAGP N RGD:5509061 20220106 MGI PMID:26911675 1557614 Il25 interleukin 25 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:16606667 1557614 Il25 interleukin 25 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20160526 MGI PMID:25888259 1557614 Il25 interleukin 25 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1557614 Il25 interleukin 25 gene MP:0001147 small testis IEA N RGD:5509061 20230119 MGI 1557614 Il25 interleukin 25 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 1557614 Il25 interleukin 25 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230119 MGI 1557614 Il25 interleukin 25 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1557614 Il25 interleukin 25 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20141003 MGI 1557614 Il25 interleukin 25 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:16606667 1557614 Il25 interleukin 25 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:20154671 1557614 Il25 interleukin 25 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1557614 Il25 interleukin 25 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20160526 MGI PMID:25888259 1557614 Il25 interleukin 25 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16606668 1557614 Il25 interleukin 25 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1557614 Il25 interleukin 25 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16606667 1557614 Il25 interleukin 25 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:17200411 1557614 Il25 interleukin 25 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16606668 1557614 Il25 interleukin 25 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20160526 MGI PMID:25888259 1557614 Il25 interleukin 25 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17200411 1557614 Il25 interleukin 25 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:16606667 1557614 Il25 interleukin 25 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:16606667 1557614 Il25 interleukin 25 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:16606668 1557614 Il25 interleukin 25 gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:16606668 1557614 Il25 interleukin 25 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:20154671 1557614 Il25 interleukin 25 gene MP:0008091 decreased T-helper 2 cell number IAGP N RGD:5509061 20160526 MGI PMID:25888259 1557614 Il25 interleukin 25 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16606667 1557614 Il25 interleukin 25 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20160526 MGI PMID:25888259 1557614 Il25 interleukin 25 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20160526 MGI PMID:25888259 1557614 Il25 interleukin 25 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:16606668 1557614 Il25 interleukin 25 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20160526 MGI PMID:25888259 1557614 Il25 interleukin 25 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20160526 MGI PMID:25888259 1557614 Il25 interleukin 25 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:16606668 1557614 Il25 interleukin 25 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:20154671 1557614 Il25 interleukin 25 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20160526 MGI PMID:25888259 1557614 Il25 interleukin 25 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20154671 1557614 Il25 interleukin 25 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20160526 MGI PMID:25888259 1557614 Il25 interleukin 25 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:16606668 1557614 Il25 interleukin 25 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:20154671 1557614 Il25 interleukin 25 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20160526 MGI PMID:25888259 1557614 Il25 interleukin 25 gene MP:0008712 decreased interleukin-9 secretion IAGP N RGD:5509061 20141003 MGI PMID:20154671 1557614 Il25 interleukin 25 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20160526 MGI PMID:25888259 1557614 Il25 interleukin 25 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:16606667 1557614 Il25 interleukin 25 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:16606667 1557614 Il25 interleukin 25 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:17200411 1557614 Il25 interleukin 25 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17200411 1557614 Il25 interleukin 25 gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20160526 MGI PMID:25888259 1557614 Il25 interleukin 25 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20231207 MGI 1557615 Mllt1 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:12781363 1557615 Mllt1 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12781363 1557615 Mllt1 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16096649 1557615 Mllt1 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:12781363 1557615 Mllt1 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:16096649 1557615 Mllt1 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12781363 1557615 Mllt1 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12367585 1557615 Mllt1 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:16096649 1557615 Mllt1 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:16096649 1557615 Mllt1 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:12781363 1557615 Mllt1 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1 gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16096649 1557615 Mllt1 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12367585 1557616 Bmx BMX non-receptor tyrosine kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11416142 1557616 Bmx BMX non-receptor tyrosine kinase gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:21471444 1557617 Nectin4 nectin cell adhesion molecule 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1557617 Nectin4 nectin cell adhesion molecule 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1557617 Nectin4 nectin cell adhesion molecule 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557622 Wdr13 WD repeat domain 13 gene MP:0001260 increased body weight IAGP N RGD:5509061 20151119 MGI PMID:22715406 1557622 Wdr13 WD repeat domain 13 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20151119 MGI PMID:22715406 1557622 Wdr13 WD repeat domain 13 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20151119 MGI PMID:22715406 1557622 Wdr13 WD repeat domain 13 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20151119 MGI PMID:22715406 1557622 Wdr13 WD repeat domain 13 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20151119 MGI PMID:22715406 1557622 Wdr13 WD repeat domain 13 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20151119 MGI PMID:22715406 1557622 Wdr13 WD repeat domain 13 gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20151119 MGI PMID:22715406 1557622 Wdr13 WD repeat domain 13 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20151119 MGI PMID:22715406 1557622 Wdr13 WD repeat domain 13 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20151119 MGI PMID:22715406 1557622 Wdr13 WD repeat domain 13 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20151119 MGI PMID:22715406 1557622 Wdr13 WD repeat domain 13 gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20151119 MGI PMID:22715406 1557623 Hhip Hedgehog-interacting protein gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12917290 1557623 Hhip Hedgehog-interacting protein gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12917290 1557623 Hhip Hedgehog-interacting protein gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:12917290 1557623 Hhip Hedgehog-interacting protein gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15576403 1557623 Hhip Hedgehog-interacting protein gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:15576403 1557623 Hhip Hedgehog-interacting protein gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12569124 1557623 Hhip Hedgehog-interacting protein gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:15576403 1557623 Hhip Hedgehog-interacting protein gene MP:0001699 increased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15576403 1557623 Hhip Hedgehog-interacting protein gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:12569124 1557623 Hhip Hedgehog-interacting protein gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15576403 1557623 Hhip Hedgehog-interacting protein gene MP:0002271 abnormal pulmonary alveolar duct morphology IAGP N RGD:5509061 20141003 MGI PMID:12569124 1557623 Hhip Hedgehog-interacting protein gene MP:0002271 abnormal pulmonary alveolar duct morphology IAGP N RGD:5509061 20141003 MGI PMID:15576403 1557623 Hhip Hedgehog-interacting protein gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:15576403 1557623 Hhip Hedgehog-interacting protein gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:12569124 1557623 Hhip Hedgehog-interacting protein gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:12569124 1557623 Hhip Hedgehog-interacting protein gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:12917290 1557623 Hhip Hedgehog-interacting protein gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:12917290 1557623 Hhip Hedgehog-interacting protein gene MP:0004979 abnormal neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:15576403 1557623 Hhip Hedgehog-interacting protein gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:15576403 1557623 Hhip Hedgehog-interacting protein gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:12917290 1557623 Hhip Hedgehog-interacting protein gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15576403 1557623 Hhip Hedgehog-interacting protein gene MP:0006343 enlarged first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15576403 1557623 Hhip Hedgehog-interacting protein gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:12917290 1557623 Hhip Hedgehog-interacting protein gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:12917290 1557623 Hhip Hedgehog-interacting protein gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:12569124 1557623 Hhip Hedgehog-interacting protein gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12569124 1557623 Hhip Hedgehog-interacting protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12917290 1557623 Hhip Hedgehog-interacting protein gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15576403 1557623 Hhip Hedgehog-interacting protein gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20150611 MGI PMID:12917290 1557623 Hhip Hedgehog-interacting protein gene MP:0011934 abnormal branching involved in pancreas development IAGP N RGD:5509061 20141218 MGI PMID:12917290 1557623 Hhip Hedgehog-interacting protein gene MP:0012675 enlarged floor plate IAGP N RGD:5509061 20141003 MGI PMID:15576403 1557623 Hhip Hedgehog-interacting protein gene MP:0013291 ectopic pancreas IAGP N RGD:5509061 20141218 MGI PMID:12917290 1557624 Syncrip synaptotagmin binding, cytoplasmic RNA interacting protein gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210520 MGI 1557624 Syncrip synaptotagmin binding, cytoplasmic RNA interacting protein gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 1557624 Syncrip synaptotagmin binding, cytoplasmic RNA interacting protein gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210520 MGI 1557624 Syncrip synaptotagmin binding, cytoplasmic RNA interacting protein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1557624 Syncrip synaptotagmin binding, cytoplasmic RNA interacting protein gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1557624 Syncrip synaptotagmin binding, cytoplasmic RNA interacting protein gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210520 MGI 1557624 Syncrip synaptotagmin binding, cytoplasmic RNA interacting protein gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230601 MGI 1557624 Syncrip synaptotagmin binding, cytoplasmic RNA interacting protein gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210826 MGI 1557624 Syncrip synaptotagmin binding, cytoplasmic RNA interacting protein gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1557624 Syncrip synaptotagmin binding, cytoplasmic RNA interacting protein gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20240523 MGI 1557624 Syncrip synaptotagmin binding, cytoplasmic RNA interacting protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1557624 Syncrip synaptotagmin binding, cytoplasmic RNA interacting protein gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210520 MGI 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0000531 right pulmonary isomerism IEA N RGD:5509061 20210218 MGI 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210218 MGI 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0000644 dextrocardia IEA N RGD:5509061 20210218 MGI 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0000650 mesocardia IEA N RGD:5509061 20210218 MGI 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16581775 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20210218 MGI 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:16581775 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23706739 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16581775 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0004133 heterotaxia IEA N RGD:5509061 20210218 MGI 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0004158 right aortic arch IEA N RGD:5509061 20210218 MGI 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16581775 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0006123 tricuspid valve atresia IEA N RGD:5509061 20210218 MGI 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16581775 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16581775 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:16581775 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:23706739 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20210218 MGI 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20210218 MGI 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0011665 d-loop transposition of the great arteries IEA N RGD:5509061 20210218 MGI 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0011668 double outlet right ventricle, Taussig bing type IEA N RGD:5509061 20210218 MGI 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20210218 MGI 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:23706739 1557625 Psme4 proteasome (prosome, macropain) activator subunit 4 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:16581775 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20230803 MGI PMID:36698249 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20230330 MGI PMID:32665638 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20230420 MGI PMID:36930220 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20230803 MGI PMID:36698249 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20230803 MGI PMID:36698249 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0003064 decreased coping response IEA N RGD:5509061 20210128 MGI 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230420 MGI PMID:36930220 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230803 MGI PMID:36698249 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20230803 MGI PMID:36698249 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20230330 MGI PMID:32665638 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20230420 MGI PMID:36930220 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20230420 MGI PMID:36930220 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20230803 MGI PMID:36698249 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20230803 MGI PMID:36698249 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20230330 MGI PMID:32665638 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20230803 MGI PMID:36698249 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20230420 MGI PMID:36930220 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20230803 MGI PMID:36698249 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20230420 MGI PMID:36930220 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20230803 MGI PMID:36698249 1557626 Adad2 adenosine deaminase domain containing 2 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20230803 MGI PMID:36698249 1557629 Zfp92 zinc finger protein 92 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1557629 Zfp92 zinc finger protein 92 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1557629 Zfp92 zinc finger protein 92 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1557629 Zfp92 zinc finger protein 92 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1557629 Zfp92 zinc finger protein 92 gene MP:0010768 mortality/aging IAGP N RGD:5509061 20210701 MGI PMID:33653874 1557630 St6galnac2 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557630 St6galnac2 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557630 St6galnac2 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557630 St6galnac2 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557630 St6galnac2 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557630 St6galnac2 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557630 St6galnac2 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557630 St6galnac2 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557631 Cep192 centrosomal protein 192 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20231109 MGI PMID:36325906 1557631 Cep192 centrosomal protein 192 gene MP:0008823 abnormal interventricular septum membranous part morphology IAGP N RGD:5509061 20231109 MGI PMID:36325906 1557631 Cep192 centrosomal protein 192 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20231109 MGI PMID:36325906 1557631 Cep192 centrosomal protein 192 gene MP:0010498 abnormal interventricular septum muscular part morphology IAGP N RGD:5509061 20231109 MGI PMID:36325906 1557632 Fem1a fem 1 homolog a gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20180503 MGI PMID:26439841 1557632 Fem1a fem 1 homolog a gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20180503 MGI PMID:26439841 1557632 Fem1a fem 1 homolog a gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180503 MGI PMID:26439841 1557632 Fem1a fem 1 homolog a gene MP:0003269 colon polyps IAGP N RGD:5509061 20180503 MGI PMID:26439841 1557632 Fem1a fem 1 homolog a gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20180503 MGI PMID:26439841 1557632 Fem1a fem 1 homolog a gene MP:0012436 increased colon tumor incidence IAGP N RGD:5509061 20180503 MGI PMID:26439841 1557632 Fem1a fem 1 homolog a gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20180503 MGI PMID:26439841 1557632 Fem1a fem 1 homolog a gene MP:0013956 decreased colon length IAGP N RGD:5509061 20180503 MGI PMID:26439841 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20180222 MGI PMID:27153923 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:15755804 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21539826 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15755804 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:21539826 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0002083 premature death IAGP N RGD:5509061 20180222 MGI PMID:27153923 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:27153923 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20200102 MGI PMID:30573647 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:21539826 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20180222 MGI PMID:27153923 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20180222 MGI PMID:27153923 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0003606 kidney failure IAGP N RGD:5509061 20180222 MGI PMID:27153923 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0003675 kidney cyst IAGP N RGD:5509061 20180222 MGI PMID:27153923 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20200102 MGI PMID:30573647 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20180222 MGI PMID:27153923 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20180222 MGI PMID:27153923 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20180222 MGI PMID:27153923 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20180222 MGI PMID:27153923 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200102 MGI PMID:30573647 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20180222 MGI PMID:27153923 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20200102 MGI PMID:30573647 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200102 MGI PMID:30573647 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20200102 MGI PMID:30573647 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21539826 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21539826 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20180222 MGI PMID:27153923 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20180222 MGI PMID:27153923 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200102 MGI PMID:30573647 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200102 MGI PMID:30573647 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20200102 MGI PMID:30573647 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0020384 absent kidney epithelial cell primary cilium IAGP N RGD:5509061 20180222 MGI PMID:27153923 1557633 Arl13b ADP-ribosylation factor-like 13B gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20200102 MGI PMID:30573647 1557635 Hs6st2 heparan sulfate 6-O-sulfotransferase 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18281280 1557635 Hs6st2 heparan sulfate 6-O-sulfotransferase 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1557636 Cd300c2 CD300C molecule 2 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21727189 1557637 Hook3 hook microtubule tethering protein 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20170105 MGI 1557637 Hook3 hook microtubule tethering protein 3 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20170105 MGI 1557637 Hook3 hook microtubule tethering protein 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20170105 MGI 1557637 Hook3 hook microtubule tethering protein 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20170105 MGI 1557637 Hook3 hook microtubule tethering protein 3 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20221215 MGI 1557637 Hook3 hook microtubule tethering protein 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20170105 MGI 1557637 Hook3 hook microtubule tethering protein 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1557637 Hook3 hook microtubule tethering protein 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1557637 Hook3 hook microtubule tethering protein 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20170105 MGI 1557637 Hook3 hook microtubule tethering protein 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20181227 MGI 1557637 Hook3 hook microtubule tethering protein 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20170105 MGI 1557638 Acsbg1 acyl-CoA synthetase bubblegum family member 1 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20200310 MGI PMID:19167491 1557638 Acsbg1 acyl-CoA synthetase bubblegum family member 1 gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20200310 MGI PMID:19167491 1557638 Acsbg1 acyl-CoA synthetase bubblegum family member 1 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20200310 MGI PMID:19167491 1557638 Acsbg1 acyl-CoA synthetase bubblegum family member 1 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:19167491 1557638 Acsbg1 acyl-CoA synthetase bubblegum family member 1 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:19167491 1557639 Ciapin1 cytokine induced apoptosis inhibitor 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:14970183 1557639 Ciapin1 cytokine induced apoptosis inhibitor 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:14970183 1557639 Ciapin1 cytokine induced apoptosis inhibitor 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:14970183 1557639 Ciapin1 cytokine induced apoptosis inhibitor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14970183 1557639 Ciapin1 cytokine induced apoptosis inhibitor 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14970183 1557639 Ciapin1 cytokine induced apoptosis inhibitor 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:14970183 1557639 Ciapin1 cytokine induced apoptosis inhibitor 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14970183 1557639 Ciapin1 cytokine induced apoptosis inhibitor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14970183 1557639 Ciapin1 cytokine induced apoptosis inhibitor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14970183 1557640 Ddx18 DEAD box helicase 18 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20240523 MGI 1557640 Ddx18 DEAD box helicase 18 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20210506 MGI PMID:31914400 1557640 Ddx18 DEAD box helicase 18 gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20210506 MGI PMID:31914400 1557640 Ddx18 DEAD box helicase 18 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20241017 MGI PMID:31914400 1557640 Ddx18 DEAD box helicase 18 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241017 MGI 1557640 Ddx18 DEAD box helicase 18 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20240523 MGI 1557640 Ddx18 DEAD box helicase 18 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20210506 MGI PMID:31914400 1557640 Ddx18 DEAD box helicase 18 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1557640 Ddx18 DEAD box helicase 18 gene MP:0012111 failure of morula compaction IEA N RGD:5509061 20241017 MGI 1557643 Susd4 sushi domain containing 4 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20210722 MGI PMID:32179479 1557643 Susd4 sushi domain containing 4 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20210722 MGI PMID:32179479 1557643 Susd4 sushi domain containing 4 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20210722 MGI PMID:32179479 1557643 Susd4 sushi domain containing 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210722 MGI PMID:32179479 1557643 Susd4 sushi domain containing 4 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20210722 MGI PMID:32179479 1557643 Susd4 sushi domain containing 4 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20210722 MGI PMID:32179479 1557643 Susd4 sushi domain containing 4 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20210722 MGI PMID:32179479 1557643 Susd4 sushi domain containing 4 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20210722 MGI PMID:32179479 1557643 Susd4 sushi domain containing 4 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20210722 MGI PMID:32179479 1557643 Susd4 sushi domain containing 4 gene MP:0011566 abnormal complement protein level IAGP N RGD:5509061 20210722 MGI PMID:32179479 1557643 Susd4 sushi domain containing 4 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20210722 MGI PMID:32179479 1557643 Susd4 sushi domain containing 4 gene MP:0020358 abnormal inhibitory synapse morphology IAGP N RGD:5509061 20210722 MGI PMID:32179479 1557643 Susd4 sushi domain containing 4 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20210722 MGI PMID:32179479 1557643 Susd4 sushi domain containing 4 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20210722 MGI PMID:32179479 1557644 Ptx3 pentraxin related gene gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:12040004 1557644 Ptx3 pentraxin related gene gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:14998931 1557644 Ptx3 pentraxin related gene gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:12432394 1557644 Ptx3 pentraxin related gene gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12432394 1557644 Ptx3 pentraxin related gene gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12040004 1557644 Ptx3 pentraxin related gene gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12432394 1557644 Ptx3 pentraxin related gene gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:14998931 1557644 Ptx3 pentraxin related gene gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12040004 1557644 Ptx3 pentraxin related gene gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14998931 1557644 Ptx3 pentraxin related gene gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12040004 1557644 Ptx3 pentraxin related gene gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:14998931 1557644 Ptx3 pentraxin related gene gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12432394 1557644 Ptx3 pentraxin related gene gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12432394 1557644 Ptx3 pentraxin related gene gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12432394 1557644 Ptx3 pentraxin related gene gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12432394 1557644 Ptx3 pentraxin related gene gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:12432394 1557644 Ptx3 pentraxin related gene gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:12432394 1557644 Ptx3 pentraxin related gene gene MP:0009372 abnormal cumulus oophorus morphology IAGP N RGD:5509061 20141003 MGI PMID:12040004 1557644 Ptx3 pentraxin related gene gene MP:0009372 abnormal cumulus oophorus morphology IAGP N RGD:5509061 20141003 MGI PMID:14998931 1557644 Ptx3 pentraxin related gene gene MP:0009374 absent cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:12040004 1557644 Ptx3 pentraxin related gene gene MP:0009374 absent cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:14998931 1557644 Ptx3 pentraxin related gene gene MP:0009374 absent cumulus expansion IAGP N RGD:5509061 20230518 MGI PMID:17675295 1557644 Ptx3 pentraxin related gene gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:22732935 1557644 Ptx3 pentraxin related gene gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:12040004 1557646 Ssu2 ssu-2 homolog gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20170928 MGI PMID:27680507 1557646 Ssu2 ssu-2 homolog gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20170928 MGI PMID:27680507 1557646 Ssu2 ssu-2 homolog gene MP:0002819 abnormal dental pulp cavity morphology IAGP N RGD:5509061 20170928 MGI PMID:27680507 1557646 Ssu2 ssu-2 homolog gene MP:0013250 abnormal dental pulp morphology IAGP N RGD:5509061 20180215 MGI PMID:27680507 1557646 Ssu2 ssu-2 homolog gene MP:0030451 abnormal dentin mineralization IAGP N RGD:5509061 20171221 MGI PMID:27680507 1557646 Ssu2 ssu-2 homolog gene MP:0030455 increased odontoblast number IAGP N RGD:5509061 20180215 MGI PMID:27680507 1557646 Ssu2 ssu-2 homolog gene MP:0030459 abnormal tooth attrition IAGP N RGD:5509061 20180215 MGI PMID:27680507 1557646 Ssu2 ssu-2 homolog gene MP:0030543 abnormal predentin morphology IAGP N RGD:5509061 20180215 MGI PMID:27680507 1557651 Tnni3k TNNI3 interacting kinase gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20150212 MGI PMID:24132636 1557651 Tnni3k TNNI3 interacting kinase gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20180222 MGI PMID:28783163 1557651 Tnni3k TNNI3 interacting kinase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20231102 MGI PMID:37628941 1557651 Tnni3k TNNI3 interacting kinase gene MP:0001661 extended life span IAGP N RGD:5509061 20231102 MGI PMID:19763165 1557651 Tnni3k TNNI3 interacting kinase gene MP:0002083 premature death IAGP N RGD:5509061 20231102 MGI PMID:19763165 1557651 Tnni3k TNNI3 interacting kinase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20231102 MGI PMID:37628941 1557651 Tnni3k TNNI3 interacting kinase gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20231102 MGI PMID:37628941 1557651 Tnni3k TNNI3 interacting kinase gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20231102 MGI PMID:19763165 1557651 Tnni3k TNNI3 interacting kinase gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20150212 MGI PMID:24132636 1557651 Tnni3k TNNI3 interacting kinase gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20150212 MGI PMID:24132636 1557651 Tnni3k TNNI3 interacting kinase gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20180222 MGI PMID:28783163 1557651 Tnni3k TNNI3 interacting kinase gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20231102 MGI PMID:19763165 1557651 Tnni3k TNNI3 interacting kinase gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20231102 MGI PMID:19763165 1557651 Tnni3k TNNI3 interacting kinase gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20231102 MGI PMID:37628941 1557651 Tnni3k TNNI3 interacting kinase gene MP:0005331 insulin resistance IAGP N RGD:5509061 20231102 MGI PMID:37628941 1557651 Tnni3k TNNI3 interacting kinase gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20231102 MGI PMID:19763165 1557651 Tnni3k TNNI3 interacting kinase gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20231102 MGI PMID:37628941 1557651 Tnni3k TNNI3 interacting kinase gene MP:0006321 increased myocardial fiber number IAGP N RGD:5509061 20180222 MGI PMID:28783163 1557651 Tnni3k TNNI3 interacting kinase gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231102 MGI PMID:37628941 1557652 Hoxa3 homeobox A3 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0000678 abnormal parathyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1557652 Hoxa3 homeobox A3 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20150305 MGI PMID:14623825 1557652 Hoxa3 homeobox A3 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9520319 1557652 Hoxa3 homeobox A3 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:10688203 1557652 Hoxa3 homeobox A3 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:7913519 1557652 Hoxa3 homeobox A3 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:14960494 1557652 Hoxa3 homeobox A3 gene MP:0001051 abnormal somatic motor system morphology IAGP N RGD:5509061 20141003 MGI PMID:12954718 1557652 Hoxa3 homeobox A3 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14623825 1557652 Hoxa3 homeobox A3 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10688203 1557652 Hoxa3 homeobox A3 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10688203 1557652 Hoxa3 homeobox A3 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0002249 abnormal larynx morphology IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0002256 abnormal laryngeal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16696966 1557652 Hoxa3 homeobox A3 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1557652 Hoxa3 homeobox A3 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20141003 MGI PMID:14623825 1557652 Hoxa3 homeobox A3 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20141003 MGI PMID:9520319 1557652 Hoxa3 homeobox A3 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10688203 1557652 Hoxa3 homeobox A3 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0003154 abnormal soft palate morphology IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0003445 sirenomelia IAGP N RGD:5509061 20150716 MGI PMID:23028455 1557652 Hoxa3 homeobox A3 gene MP:0003494 parathyroid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14623825 1557652 Hoxa3 homeobox A3 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20171102 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0003955 abnormal ultimobranchial body morphology IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0003955 abnormal ultimobranchial body morphology IAGP N RGD:5509061 20141003 MGI PMID:9520319 1557652 Hoxa3 homeobox A3 gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0004445 small exoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0004549 small trachea IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0004568 fusion of glossopharyngeal and vagus nerve IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0004568 fusion of glossopharyngeal and vagus nerve IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0004914 absent ultimobranchial body IAGP N RGD:5509061 20150122 MGI PMID:9520319 1557652 Hoxa3 homeobox A3 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12954718 1557652 Hoxa3 homeobox A3 gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0006340 abnormal fourth pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1557652 Hoxa3 homeobox A3 gene MP:0009052 anal stenosis IAGP N RGD:5509061 20150716 MGI PMID:23028455 1557652 Hoxa3 homeobox A3 gene MP:0009252 absent urinary bladder IAGP N RGD:5509061 20150716 MGI PMID:23028455 1557652 Hoxa3 homeobox A3 gene MP:0009844 abnormal neural crest cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14623825 1557652 Hoxa3 homeobox A3 gene MP:0009913 abnormal hyoid bone greater horn morphology IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0009913 abnormal hyoid bone greater horn morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0009915 absent hyoid bone lesser horns IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0009915 absent hyoid bone lesser horns IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0010371 abnormal epiglottis morphology IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0010441 total anomalous pulmonary venous connection IAGP N RGD:5509061 20231109 MGI PMID:20071345 1557652 Hoxa3 homeobox A3 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:14623825 1557652 Hoxa3 homeobox A3 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20141003 MGI PMID:14623825 1557652 Hoxa3 homeobox A3 gene MP:0010527 bicuspid pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0010541 aorta hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0010548 abnormal dorsal mesocardium morphology IAGP N RGD:5509061 20231109 MGI PMID:20071345 1557652 Hoxa3 homeobox A3 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:14623825 1557652 Hoxa3 homeobox A3 gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14623825 1557652 Hoxa3 homeobox A3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0011576 absent cervical atlas IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0011683 dual inferior vena cava IAGP N RGD:5509061 20231109 MGI PMID:20071345 1557652 Hoxa3 homeobox A3 gene MP:0012491 larynx stenosis IAGP N RGD:5509061 20141003 MGI PMID:1673020 1557652 Hoxa3 homeobox A3 gene MP:0013162 abnormal thyroid gland isthmus morphology IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0013162 abnormal thyroid gland isthmus morphology IAGP N RGD:5509061 20141003 MGI PMID:9520319 1557652 Hoxa3 homeobox A3 gene MP:0013163 absent thyroid gland isthmus IAGP N RGD:5509061 20141003 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0013163 absent thyroid gland isthmus IAGP N RGD:5509061 20141003 MGI PMID:9520319 1557652 Hoxa3 homeobox A3 gene MP:0013290 persistent ultimobranchial bodies IAGP N RGD:5509061 20150122 MGI PMID:9520319 1557652 Hoxa3 homeobox A3 gene MP:0013574 ectopic parathyroid gland IAGP N RGD:5509061 20150305 MGI PMID:14623825 1557652 Hoxa3 homeobox A3 gene MP:0013574 ectopic parathyroid gland IAGP N RGD:5509061 20150305 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0013574 ectopic parathyroid gland IAGP N RGD:5509061 20150305 MGI PMID:9520319 1557652 Hoxa3 homeobox A3 gene MP:0030291 short soft palate IAGP N RGD:5509061 20171102 MGI PMID:20498049 1557652 Hoxa3 homeobox A3 gene MP:0030337 enlarged third pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:14623825 1557652 Hoxa3 homeobox A3 gene MP:0030869 thyroid cartilage hypoplasia IAGP N RGD:5509061 20181101 MGI PMID:9441667 1557652 Hoxa3 homeobox A3 gene MP:0030872 small cricoid cartilage IAGP N RGD:5509061 20181101 MGI PMID:9441667 1557655 Sympk symplekin gene MP:0001577 anemia IEA N RGD:5509061 20111116 MGI 1557655 Sympk symplekin gene MP:0002192 hydrops fetalis IEA N RGD:5509061 20111116 MGI 1557655 Sympk symplekin gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1557656 Onecut2 one cut domain, family member 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16103213 1557656 Onecut2 one cut domain, family member 2 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:16103213 1557656 Onecut2 one cut domain, family member 2 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:17400205 1557656 Onecut2 one cut domain, family member 2 gene MP:0012242 abnormal hepatoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:16103213 1557656 Onecut2 one cut domain, family member 2 gene MP:0012246 abnormal hepatic cord morphology IAGP N RGD:5509061 20141003 MGI PMID:16103213 1557657 Gorab golgin, RAB6-interacting gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20160707 MGI PMID:26967474 1557657 Gorab golgin, RAB6-interacting gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20160707 MGI PMID:26967474 1557657 Gorab golgin, RAB6-interacting gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20160707 MGI PMID:26967474 1557657 Gorab golgin, RAB6-interacting gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20160707 MGI PMID:26967474 1557657 Gorab golgin, RAB6-interacting gene MP:0001505 hunched posture IAGP N RGD:5509061 20160707 MGI PMID:26967474 1557657 Gorab golgin, RAB6-interacting gene MP:0001786 skin edema IAGP N RGD:5509061 20160707 MGI PMID:26967474 1557657 Gorab golgin, RAB6-interacting gene MP:0001954 respiratory distress IAGP N RGD:5509061 20160707 MGI PMID:26967474 1557657 Gorab golgin, RAB6-interacting gene MP:0009545 abnormal dermis papillary layer morphology IAGP N RGD:5509061 20160707 MGI PMID:26967474 1557657 Gorab golgin, RAB6-interacting gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160707 MGI PMID:26967474 1557657 Gorab golgin, RAB6-interacting gene MP:0013205 abnormal nonmotile primary cilium morphology IAGP N RGD:5509061 20160707 MGI PMID:26967474 1557658 Dnajc5b DnaJ heat shock protein family (Hsp40) member C5 beta gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1557658 Dnajc5b DnaJ heat shock protein family (Hsp40) member C5 beta gene MP:0003900 shortened QT interval IEA N RGD:5509061 20160421 MGI 1557658 Dnajc5b DnaJ heat shock protein family (Hsp40) member C5 beta gene MP:0010571 shortened ST segment IEA N RGD:5509061 20210128 MGI 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0000231 hypertension IAGP N RGD:5509061 20170330 MGI PMID:27821757 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20200514 MGI 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200514 MGI 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200514 MGI 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20160204 MGI PMID:24586788 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20160204 MGI PMID:24586788 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20160204 MGI PMID:24586788 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20160204 MGI PMID:24586788 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20170330 MGI PMID:27821757 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20160204 MGI PMID:24586788 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20200514 MGI 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0002871 albuminuria IAGP N RGD:5509061 20170330 MGI PMID:27821757 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20160204 MGI PMID:24586788 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20170330 MGI PMID:27821757 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0010695 abnormal blood pressure regulation IAGP N RGD:5509061 20160204 MGI PMID:24586788 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0010935 increased airway resistance IEA N RGD:5509061 20221215 MGI 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20170330 MGI PMID:27821757 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20170330 MGI PMID:27821757 1557659 Asb4 ankyrin repeat and SOCS box-containing 4 gene MP:0020153 abnormal urine albumin level IAGP N RGD:5509061 20160204 MGI PMID:24586788 1557661 Scrn1 secernin 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 1557661 Scrn1 secernin 1 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1557662 Edar ectodysplasin-A receptor gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:270322 1557662 Edar ectodysplasin-A receptor gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:544312 1557662 Edar ectodysplasin-A receptor gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1557662 Edar ectodysplasin-A receptor gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:892445 1557662 Edar ectodysplasin-A receptor gene MP:0000372 irregular coat pigmentation IEA N RGD:5509061 20181011 MGI 1557662 Edar ectodysplasin-A receptor gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:2622338 1557662 Edar ectodysplasin-A receptor gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20150618 MGI PMID:9799834 1557662 Edar ectodysplasin-A receptor gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20141003 MGI PMID:23415220 1557662 Edar ectodysplasin-A receptor gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20141003 MGI PMID:892445 1557662 Edar ectodysplasin-A receptor gene MP:0000405 abnormal auchene hair morphology IAGP N RGD:5509061 20141003 MGI PMID:23415220 1557662 Edar ectodysplasin-A receptor gene MP:0000408 absent duvet hair IAGP N RGD:5509061 20141003 MGI PMID:892445 1557662 Edar ectodysplasin-A receptor gene MP:0000411 shiny fur IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:2622338 1557662 Edar ectodysplasin-A receptor gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:2622338 1557662 Edar ectodysplasin-A receptor gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:17148670 1557662 Edar ectodysplasin-A receptor gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:2622338 1557662 Edar ectodysplasin-A receptor gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:23415220 1557662 Edar ectodysplasin-A receptor gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:2622338 1557662 Edar ectodysplasin-A receptor gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:544312 1557662 Edar ectodysplasin-A receptor gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20150618 MGI PMID:9799834 1557662 Edar ectodysplasin-A receptor gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:17148670 1557662 Edar ectodysplasin-A receptor gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:892445 1557662 Edar ectodysplasin-A receptor gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:270322 1557662 Edar ectodysplasin-A receptor gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:544312 1557662 Edar ectodysplasin-A receptor gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:17148670 1557662 Edar ectodysplasin-A receptor gene MP:0003791 abnormal minor salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:20969842 1557662 Edar ectodysplasin-A receptor gene MP:0003849 greasy coat IAGP N RGD:5509061 20141003 MGI PMID:2622338 1557662 Edar ectodysplasin-A receptor gene MP:0003931 absent molars IAGP N RGD:5509061 20141003 MGI PMID:270322 1557662 Edar ectodysplasin-A receptor gene MP:0003931 absent molars IAGP N RGD:5509061 20141003 MGI PMID:544312 1557662 Edar ectodysplasin-A receptor gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:270322 1557662 Edar ectodysplasin-A receptor gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:544312 1557662 Edar ectodysplasin-A receptor gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:892445 1557662 Edar ectodysplasin-A receptor gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17148670 1557662 Edar ectodysplasin-A receptor gene MP:0006236 absent Meibomian glands IAGP N RGD:5509061 20141003 MGI PMID:2622338 1557662 Edar ectodysplasin-A receptor gene MP:0006236 absent Meibomian glands IAGP N RGD:5509061 20150618 MGI PMID:9799834 1557662 Edar ectodysplasin-A receptor gene MP:0006258 abnormal circumvallate papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:20969842 1557662 Edar ectodysplasin-A receptor gene MP:0006363 absent auchene hairs IAGP N RGD:5509061 20141003 MGI PMID:892445 1557662 Edar ectodysplasin-A receptor gene MP:0006365 absent guard hair IAGP N RGD:5509061 20141003 MGI PMID:17148670 1557662 Edar ectodysplasin-A receptor gene MP:0006365 absent guard hair IAGP N RGD:5509061 20141003 MGI PMID:2622338 1557662 Edar ectodysplasin-A receptor gene MP:0006365 absent guard hair IAGP N RGD:5509061 20141003 MGI PMID:892445 1557662 Edar ectodysplasin-A receptor gene MP:0006366 absent zigzag hairs IAGP N RGD:5509061 20141003 MGI PMID:17148670 1557662 Edar ectodysplasin-A receptor gene MP:0006366 absent zigzag hairs IAGP N RGD:5509061 20141003 MGI PMID:892445 1557662 Edar ectodysplasin-A receptor gene MP:0006367 absent sweat gland IAGP N RGD:5509061 20150618 MGI PMID:9799834 1557662 Edar ectodysplasin-A receptor gene MP:0006400 decreased molar number IAGP N RGD:5509061 20141003 MGI PMID:270322 1557662 Edar ectodysplasin-A receptor gene MP:0006400 decreased molar number IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0006400 decreased molar number IAGP N RGD:5509061 20141003 MGI PMID:544312 1557662 Edar ectodysplasin-A receptor gene MP:0006402 small molars IAGP N RGD:5509061 20141003 MGI PMID:270322 1557662 Edar ectodysplasin-A receptor gene MP:0006402 small molars IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0006402 small molars IAGP N RGD:5509061 20141003 MGI PMID:544312 1557662 Edar ectodysplasin-A receptor gene MP:0008904 abnormal mammary fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:23415220 1557662 Edar ectodysplasin-A receptor gene MP:0009003 abnormal vibrissa number IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0009003 abnormal vibrissa number IAGP N RGD:5509061 20141003 MGI PMID:544312 1557662 Edar ectodysplasin-A receptor gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1557662 Edar ectodysplasin-A receptor gene MP:0009533 absent palatine gland IAGP N RGD:5509061 20141003 MGI PMID:20969842 1557662 Edar ectodysplasin-A receptor gene MP:0009534 absent anterior lingual gland IAGP N RGD:5509061 20141003 MGI PMID:20969842 1557662 Edar ectodysplasin-A receptor gene MP:0010233 hairless tail IAGP N RGD:5509061 20141003 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0010233 hairless tail IAGP N RGD:5509061 20141003 MGI PMID:892445 1557662 Edar ectodysplasin-A receptor gene MP:0010864 abnormal enamel knot morphology IAGP N RGD:5509061 20141003 MGI PMID:19340299 1557662 Edar ectodysplasin-A receptor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1557662 Edar ectodysplasin-A receptor gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557662 Edar ectodysplasin-A receptor gene MP:0013176 abnormal tail position or orientation IEA N RGD:5509061 20141003 MGI 1557662 Edar ectodysplasin-A receptor gene MP:0013457 increased eccrine gland number IAGP N RGD:5509061 20150212 MGI PMID:23415220 1557662 Edar ectodysplasin-A receptor gene MP:0013458 decreased eccrine gland number IAGP N RGD:5509061 20150212 MGI PMID:23415220 1557662 Edar ectodysplasin-A receptor gene MP:0030079 small incisors IAGP N RGD:5509061 20170928 MGI PMID:270322 1557662 Edar ectodysplasin-A receptor gene MP:0030079 small incisors IAGP N RGD:5509061 20170928 MGI PMID:5361555 1557662 Edar ectodysplasin-A receptor gene MP:0030079 small incisors IAGP N RGD:5509061 20170928 MGI PMID:544312 1557662 Edar ectodysplasin-A receptor gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20180125 MGI PMID:270322 1557662 Edar ectodysplasin-A receptor gene MP:0030494 abnormal molar root morphology IAGP N RGD:5509061 20180125 MGI PMID:270322 1557665 Fancm Fanconi anemia, complementation group M gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20160304 MGI PMID:19561169 1557665 Fancm Fanconi anemia, complementation group M gene MP:0001147 small testis IAGP N RGD:5509061 20160304 MGI PMID:19561169 1557665 Fancm Fanconi anemia, complementation group M gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20160304 MGI PMID:19561169 1557665 Fancm Fanconi anemia, complementation group M gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20210311 MGI PMID:29895858 1557665 Fancm Fanconi anemia, complementation group M gene MP:0001925 male infertility IAGP N RGD:5509061 20210311 MGI PMID:29895858 1557665 Fancm Fanconi anemia, complementation group M gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20160304 MGI PMID:19561169 1557665 Fancm Fanconi anemia, complementation group M gene MP:0002083 premature death IAGP N RGD:5509061 20160304 MGI PMID:19561169 1557665 Fancm Fanconi anemia, complementation group M gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20160304 MGI PMID:19561169 1557665 Fancm Fanconi anemia, complementation group M gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20210311 MGI PMID:29895858 1557665 Fancm Fanconi anemia, complementation group M gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20160304 MGI PMID:19561169 1557665 Fancm Fanconi anemia, complementation group M gene MP:0003701 elevated level of mitotic sister chromatid exchange IAGP N RGD:5509061 20160304 MGI PMID:19561169 1557665 Fancm Fanconi anemia, complementation group M gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20160304 MGI PMID:19561169 1557665 Fancm Fanconi anemia, complementation group M gene MP:0005159 azoospermia IAGP N RGD:5509061 20160304 MGI PMID:19561169 1557665 Fancm Fanconi anemia, complementation group M gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20160304 MGI PMID:19561169 1557665 Fancm Fanconi anemia, complementation group M gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210311 MGI PMID:29895858 1557665 Fancm Fanconi anemia, complementation group M gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20160304 MGI PMID:19561169 1557665 Fancm Fanconi anemia, complementation group M gene MP:0014040 increased cellular sensitivity to DNA damaging agents IAGP N RGD:5509061 20210311 MGI PMID:29895858 1557665 Fancm Fanconi anemia, complementation group M gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20210311 MGI PMID:29895858 1557666 Golgb1 golgin B1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180503 MGI PMID:27226319 1557666 Golgb1 golgin B1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180503 MGI PMID:28509431 1557666 Golgb1 golgin B1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180503 MGI PMID:28509431 1557666 Golgb1 golgin B1 gene MP:0000445 short snout IAGP N RGD:5509061 20180503 MGI PMID:28509431 1557666 Golgb1 golgin B1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20180503 MGI PMID:28509431 1557666 Golgb1 golgin B1 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20180503 MGI PMID:27226319 1557666 Golgb1 golgin B1 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20180503 MGI PMID:27226319 1557666 Golgb1 golgin B1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20230302 MGI PMID:27226319 1557666 Golgb1 golgin B1 gene MP:0014430 decreased hyaluronic acid level IAGP N RGD:5509061 20240425 MGI PMID:27226319 1557666 Golgb1 golgin B1 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:27226319 1557666 Golgb1 golgin B1 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:27226319 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20421466 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:20421466 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:22723547 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20368430 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20421466 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20368430 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:20368430 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:20368430 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:22723547 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:22723547 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20190502 MGI PMID:27096368 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20421466 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:20368430 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:20421466 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:20368430 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20421466 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20421466 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20368430 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:20368430 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20368430 1557669 Timd4 T cell immunoglobulin and mucin domain containing 4 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20190502 MGI PMID:27096368 1557670 Phf21a PHD finger protein 21A gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:16684532 1557670 Phf21a PHD finger protein 21A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16684532 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20141003 MGI PMID:17143286 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:17143286 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:17143286 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17143286 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0000445 short snout IAGP N RGD:5509061 20171019 MGI PMID:17143286 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17143286 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17143286 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21204784 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20200514 MGI 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21204784 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:17143286 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20240523 MGI 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0006418 abnormal testis cord formation IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0009370 decreased theca cell number IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:19056881 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0011896 increased circulating unsaturated transferrin level IEA N RGD:5509061 20240523 MGI 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:17143286 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:21204784 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0030189 broad snout IAGP N RGD:5509061 20171019 MGI PMID:17143286 1557672 Plekha1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1 gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:21204784 1557673 Tprn taperin gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1557673 Tprn taperin gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20160421 MGI 1557673 Tprn taperin gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20170601 MGI PMID:27693694 1557673 Tprn taperin gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20170601 MGI PMID:27693694 1557673 Tprn taperin gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20170601 MGI PMID:27693694 1557673 Tprn taperin gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20170601 MGI PMID:27693694 1557673 Tprn taperin gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1557673 Tprn taperin gene MP:0004749 nonsyndromic hearing loss IAGP N RGD:5509061 20170803 MGI PMID:27693694 1557673 Tprn taperin gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1557673 Tprn taperin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20170601 MGI PMID:27693694 1557674 Tulp3 TUB like protein 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0000480 increased rib number IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0002809 increased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1557674 Tulp3 TUB like protein 3 gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160421 MGI 1557674 Tulp3 TUB like protein 3 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220811 MGI 1557674 Tulp3 TUB like protein 3 gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1557674 Tulp3 TUB like protein 3 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20210128 MGI 1557674 Tulp3 TUB like protein 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0006253 clinodactyly IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20160421 MGI 1557674 Tulp3 TUB like protein 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20160421 MGI 1557674 Tulp3 TUB like protein 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557674 Tulp3 TUB like protein 3 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557674 Tulp3 TUB like protein 3 gene MP:0012544 abnormal caudal neuropore morphology IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0012547 spina bifida cystica IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11406614 1557674 Tulp3 TUB like protein 3 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0012707 incomplete caudal neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:19223390 1557674 Tulp3 TUB like protein 3 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1557674 Tulp3 TUB like protein 3 gene MP:0013294 prenatal lethality prior to heart atrial septation IAGP N RGD:5509061 20200310 MGI PMID:30799240 1557675 Thyn1 thymocyte nuclear protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:31329649 1557675 Thyn1 thymocyte nuclear protein 1 gene MP:0003393 decreased cardiac output IEA N RGD:5509061 20240523 MGI 1557677 Btbd2 BTB domain containing 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20240523 MGI 1557677 Btbd2 BTB domain containing 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1557677 Btbd2 BTB domain containing 2 gene MP:0000601 small liver IEA N RGD:5509061 20210128 MGI 1557677 Btbd2 BTB domain containing 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1557677 Btbd2 BTB domain containing 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1557677 Btbd2 BTB domain containing 2 gene MP:0001513 limb grasping IEA N RGD:5509061 20201231 MGI 1557677 Btbd2 BTB domain containing 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1557677 Btbd2 BTB domain containing 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20181227 MGI 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20201231 MGI 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0001304 cataract IEA N RGD:5509061 20200402 MGI 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20200402 MGI 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20170706 MGI PMID:26405179 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20200402 MGI 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20170706 MGI PMID:26405179 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20230601 MGI 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20170706 MGI PMID:26405179 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20170706 MGI PMID:26405179 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0006241 abnormal placement of pupils IEA N RGD:5509061 20200402 MGI 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0012040 abnormal c-wave shape IAGP N RGD:5509061 20170706 MGI PMID:26405179 1557679 Adamtsl4 ADAMTS-like 4 gene MP:0031428 lens dislocation IAGP N RGD:5509061 20220714 MGI PMID:26405179 1557680 Mapkapk5 MAP kinase-activated protein kinase 5 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:17254968 1557680 Mapkapk5 MAP kinase-activated protein kinase 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17254968 1557680 Mapkapk5 MAP kinase-activated protein kinase 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14560018 1557680 Mapkapk5 MAP kinase-activated protein kinase 5 gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:17254968 1557680 Mapkapk5 MAP kinase-activated protein kinase 5 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557680 Mapkapk5 MAP kinase-activated protein kinase 5 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17254968 1557682 Angptl3 angiopoietin-like 3 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11788823 1557682 Angptl3 angiopoietin-like 3 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11788823 1557682 Angptl3 angiopoietin-like 3 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:16508209 1557682 Angptl3 angiopoietin-like 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20221103 MGI 1557682 Angptl3 angiopoietin-like 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16081640 1557682 Angptl3 angiopoietin-like 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16081640 1557682 Angptl3 angiopoietin-like 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11788823 1557682 Angptl3 angiopoietin-like 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16081640 1557682 Angptl3 angiopoietin-like 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16508209 1557682 Angptl3 angiopoietin-like 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19318355 1557682 Angptl3 angiopoietin-like 3 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:11788823 1557682 Angptl3 angiopoietin-like 3 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16508209 1557682 Angptl3 angiopoietin-like 3 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16508209 1557682 Angptl3 angiopoietin-like 3 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20221103 MGI 1557682 Angptl3 angiopoietin-like 3 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11788823 1557682 Angptl3 angiopoietin-like 3 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16508209 1557682 Angptl3 angiopoietin-like 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11788823 1557682 Angptl3 angiopoietin-like 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16081640 1557682 Angptl3 angiopoietin-like 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16508209 1557682 Angptl3 angiopoietin-like 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19318355 1557682 Angptl3 angiopoietin-like 3 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11788823 1557682 Angptl3 angiopoietin-like 3 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11788823 1557682 Angptl3 angiopoietin-like 3 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16508209 1557682 Angptl3 angiopoietin-like 3 gene MP:0009709 hydrometra IEA N RGD:5509061 20221103 MGI 1557682 Angptl3 angiopoietin-like 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16081640 1557682 Angptl3 angiopoietin-like 3 gene MP:0011578 increased lipoprotein lipase activity IAGP N RGD:5509061 20141003 MGI PMID:11788823 1557682 Angptl3 angiopoietin-like 3 gene MP:0011578 increased lipoprotein lipase activity IAGP N RGD:5509061 20141003 MGI PMID:16081640 1557682 Angptl3 angiopoietin-like 3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20221103 MGI 1557686 Fam107b family with sequence similarity 107, member B gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20160804 MGI 1557686 Fam107b family with sequence similarity 107, member B gene MP:0000452 abnormal mouth morphology IEA N RGD:5509061 20160804 MGI 1557686 Fam107b family with sequence similarity 107, member B gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1557686 Fam107b family with sequence similarity 107, member B gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20160804 MGI 1557686 Fam107b family with sequence similarity 107, member B gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:23870131 1557689 Armcx3 armadillo repeat containing, X-linked 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20240328 MGI PMID:33807672 1557689 Armcx3 armadillo repeat containing, X-linked 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20240328 MGI PMID:33807672 1557689 Armcx3 armadillo repeat containing, X-linked 3 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20240328 MGI PMID:33807672 1557689 Armcx3 armadillo repeat containing, X-linked 3 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20240328 MGI PMID:33807672 1557689 Armcx3 armadillo repeat containing, X-linked 3 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20240328 MGI PMID:33807672 1557689 Armcx3 armadillo repeat containing, X-linked 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240328 MGI PMID:33807672 1557689 Armcx3 armadillo repeat containing, X-linked 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20240328 MGI PMID:33807672 1557689 Armcx3 armadillo repeat containing, X-linked 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20240328 MGI PMID:33807672 1557689 Armcx3 armadillo repeat containing, X-linked 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20240328 MGI PMID:33807672 1557689 Armcx3 armadillo repeat containing, X-linked 3 gene MP:0011939 increased food intake IAGP N RGD:5509061 20240328 MGI PMID:33807672 1557689 Armcx3 armadillo repeat containing, X-linked 3 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240328 MGI PMID:33807672 1557690 Rab7b RAB7B, member RAS oncogene family gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20220331 MGI PMID:34494097 1557690 Rab7b RAB7B, member RAS oncogene family gene MP:0020349 abnormal dendritic cell migration IAGP N RGD:5509061 20220331 MGI PMID:34494097 1557691 Bcl2l14 BCL2 like 14 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201119 MGI PMID:23059823 1557691 Bcl2l14 BCL2 like 14 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20201119 MGI PMID:31296963 1557691 Bcl2l14 BCL2 like 14 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20201119 MGI PMID:31296963 1557691 Bcl2l14 BCL2 like 14 gene MP:0012436 increased colon tumor incidence IAGP N RGD:5509061 20201119 MGI PMID:31296963 1557691 Bcl2l14 BCL2 like 14 gene MP:0013296 abnormal susceptibility to induced colitis IAGP N RGD:5509061 20201119 MGI PMID:31296963 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:23178125 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:9515964 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20190307 MGI PMID:25625206 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:23178125 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:9515963 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20231207 MGI PMID:33846290 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:23824573 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20210715 MGI PMID:31118289 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20190912 MGI PMID:28172500 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:21597012 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:23824573 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9515964 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23178125 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:23824573 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:9515964 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9515963 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9515963 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:9515963 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:9515964 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21464221 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23824573 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:15166096 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:33773996 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:34767447 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20190307 MGI PMID:25625206 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21464221 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21464221 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20190307 MGI PMID:25625206 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:21597012 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:9515964 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20190307 MGI PMID:25625206 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:9515964 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0003865 lymph node inflammation IAGP N RGD:5509061 20141003 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23178125 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0004595 abnormal mandibular condyloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0004791 absent lower incisors IAGP N RGD:5509061 20141003 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21464221 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20240530 MGI PMID:32986812 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:21464221 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20240523 MGI 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20240530 MGI PMID:32986812 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21464221 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21464221 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:9515964 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0005673 decreased susceptibility to graft versus host disease IAGP N RGD:5509061 20240530 MGI PMID:32986812 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:23824573 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0006049 semilunar valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:15166096 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0006120 mitral valve prolapse IAGP N RGD:5509061 20210715 MGI PMID:31118289 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:21597012 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:9515963 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20190307 MGI PMID:25625206 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20190307 MGI PMID:25625206 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:21464221 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21464221 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:21464221 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:21464221 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008559 abnormal interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20240530 MGI PMID:32986812 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21464221 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20240530 MGI PMID:32986812 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008686 abnormal interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20240530 MGI PMID:32986812 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:21464221 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:9462518 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21464221 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20190912 MGI PMID:28172500 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20231207 MGI PMID:33846290 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0009382 abnormal cardiac jelly morphology IAGP N RGD:5509061 20190307 MGI PMID:25625206 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23178125 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9515964 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20231207 MGI PMID:33846290 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010414 partial atrioventricular septal defect IAGP N RGD:5509061 20231207 MGI PMID:33846290 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010453 abnormal coronary vein morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010482 abnormal aortic sinus morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010595 abnormal aortic valve cusp morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010597 absent aortic valve cusps IAGP N RGD:5509061 20141003 MGI PMID:9515964 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010602 abnormal pulmonary valve cusp morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010604 absent pulmonary valve cusps IAGP N RGD:5509061 20141003 MGI PMID:9515964 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010614 abnormal mitral valve cusp morphology IAGP N RGD:5509061 20210715 MGI PMID:31118289 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010614 abnormal mitral valve cusp morphology IAGP N RGD:5509061 20240104 MGI PMID:9515963 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010622 abnormal tricuspid valve cusp morphology IAGP N RGD:5509061 20240104 MGI PMID:9515963 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010656 thick myocardium IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:22573816 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23178125 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23824573 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9515963 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9515964 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190307 MGI PMID:25625206 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0011648 thick heart valve cusps IAGP N RGD:5509061 20160107 MGI PMID:26100917 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0013206 abnormal motile cilium morphology IAGP N RGD:5509061 20210715 MGI PMID:31118289 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:9515963 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:21464221 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20240523 MGI 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0030083 long upper incisors IAGP N RGD:5509061 20170928 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0030089 short lower incisors IAGP N RGD:5509061 20170928 MGI PMID:18846253 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20231207 MGI PMID:33846290 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0031551 abnormal mitral valve development IAGP N RGD:5509061 20240104 MGI PMID:9515963 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0031552 abnormal tricuspid valve development IAGP N RGD:5509061 20240104 MGI PMID:9515963 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0031553 abnormal semilunar valve development IAGP N RGD:5509061 20240104 MGI PMID:9515963 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0031572 small atrioventricular valve IAGP N RGD:5509061 20240125 MGI PMID:23824573 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0031582 small semilunar valve IAGP N RGD:5509061 20240125 MGI PMID:23824573 1557692 Nfatc1 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 gene MP:0031593 decreased cardiac jelly amount IAGP N RGD:5509061 20240229 MGI PMID:25625206 1557693 Dock4 dedicator of cytokinesis 4 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230119 MGI 1557693 Dock4 dedicator of cytokinesis 4 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20230119 MGI 1557693 Dock4 dedicator of cytokinesis 4 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20230119 MGI 1557693 Dock4 dedicator of cytokinesis 4 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230119 MGI 1557693 Dock4 dedicator of cytokinesis 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230119 MGI 1557693 Dock4 dedicator of cytokinesis 4 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20160616 MGI PMID:26129894 1557693 Dock4 dedicator of cytokinesis 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160616 MGI PMID:26129894 1557693 Dock4 dedicator of cytokinesis 4 gene MP:0020373 abnormal blood vessel lumen formation IAGP N RGD:5509061 20170713 MGI PMID:26129894 1557693 Dock4 dedicator of cytokinesis 4 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230119 MGI 1557694 Zfp296 zinc finger protein 296 gene MP:0001127 small ovary IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0001147 small testis IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0001925 male infertility IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0001926 female infertility IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0008391 abnormal primordial germ cell morphology IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20190404 MGI PMID:28963472 1557694 Zfp296 zinc finger protein 296 gene MP:0030934 decreased primordial germ cell proliferation IAGP N RGD:5509061 20190411 MGI PMID:28963472 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:15746429 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:20403327 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:20403327 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:20403327 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:9250484 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:20403327 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:20403327 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:15746429 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:9250484 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9250484 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15746429 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20403327 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0003454 erythroderma IAGP N RGD:5509061 20141003 MGI PMID:20403327 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0003663 abnormal thermosensation IAGP N RGD:5509061 20141003 MGI PMID:15746429 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:20403327 1557695 Trpv3 transient receptor potential cation channel, subfamily V, member 3 gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20141003 MGI PMID:20403327 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:11884614 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11884614 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11884614 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11884614 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:11884614 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11884614 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11884614 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11884614 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11884614 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:11884614 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:11884614 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14645526 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14645526 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14645526 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14645526 1557696 Siah1a siah E3 ubiquitin protein ligase 1A gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11884614 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19861679 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19861679 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19861679 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:19861679 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19861679 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20160804 MGI 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0001314 cornea opacity IEA N RGD:5509061 20160804 MGI 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19861679 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:19861679 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002700 increased opacity of vitreous body IAGP N RGD:5509061 20141003 MGI PMID:23870131 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20160804 MGI 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:19861679 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0003062 abnormal coping response IEA N RGD:5509061 20160804 MGI 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20141003 MGI 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20141003 MGI 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19861679 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19861679 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:19861679 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160804 MGI 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19861679 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19861679 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:19861679 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20160804 MGI 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0008821 increased blood uric acid level IEA N RGD:5509061 20160804 MGI 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0009859 eye opacity IAGP N RGD:5509061 20141003 MGI PMID:23870131 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20141003 MGI 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0010178 increased number of Howell-Jolly bodies IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24218140 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24255920 1557697 Asxl1 ASXL transcriptional regulator 1 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23870131 1557698 Itm2b integral membrane protein 2B gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:21098268 1557698 Itm2b integral membrane protein 2B gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21098268 1557698 Itm2b integral membrane protein 2B gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18753367 1557698 Itm2b integral membrane protein 2B gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:21048150 1557698 Itm2b integral membrane protein 2B gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21048150 1557698 Itm2b integral membrane protein 2B gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21098268 1557698 Itm2b integral membrane protein 2B gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:21048150 1557698 Itm2b integral membrane protein 2B gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:21048150 1557698 Itm2b integral membrane protein 2B gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:21098268 1557703 Ier5l immediate early response 5-like gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 1557703 Ier5l immediate early response 5-like gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 1557703 Ier5l immediate early response 5-like gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20221215 MGI 1557703 Ier5l immediate early response 5-like gene MP:0002833 increased heart weight IEA N RGD:5509061 20220811 MGI 1557703 Ier5l immediate early response 5-like gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20231207 MGI 1557703 Ier5l immediate early response 5-like gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1557703 Ier5l immediate early response 5-like gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1557703 Ier5l immediate early response 5-like gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1557704 Hdgfl3 HDGF like 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20210826 MGI 1557704 Hdgfl3 HDGF like 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1557704 Hdgfl3 HDGF like 3 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20201022 MGI 1557704 Hdgfl3 HDGF like 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1557704 Hdgfl3 HDGF like 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1557704 Hdgfl3 HDGF like 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210520 MGI 1557704 Hdgfl3 HDGF like 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1557704 Hdgfl3 HDGF like 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200402 MGI 1557704 Hdgfl3 HDGF like 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 1557704 Hdgfl3 HDGF like 3 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1557707 Clxn calaxin gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20190919 MGI PMID:31240264 1557707 Clxn calaxin gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20190919 MGI PMID:31240264 1557707 Clxn calaxin gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20190919 MGI PMID:31240264 1557707 Clxn calaxin gene MP:0001935 decreased litter size IAGP N RGD:5509061 20190919 MGI PMID:31240264 1557707 Clxn calaxin gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20190919 MGI PMID:31240264 1557707 Clxn calaxin gene MP:0002766 situs inversus IAGP N RGD:5509061 20190919 MGI PMID:31240264 1557707 Clxn calaxin gene MP:0004131 abnormal motile primary cilium morphology IAGP N RGD:5509061 20190919 MGI PMID:31240264 1557707 Clxn calaxin gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20190919 MGI PMID:31240264 1557707 Clxn calaxin gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20190919 MGI PMID:31240264 1557707 Clxn calaxin gene MP:0008933 abnormal motile primary cilium physiology IAGP N RGD:5509061 20190919 MGI PMID:31240264 1557707 Clxn calaxin gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20190919 MGI PMID:31240264 1557707 Clxn calaxin gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20190919 MGI PMID:31240264 1557707 Clxn calaxin gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20190919 MGI PMID:31240264 1557707 Clxn calaxin gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20190919 MGI PMID:31240264 1557707 Clxn calaxin gene MP:0013197 decreased embryonic cilium number IAGP N RGD:5509061 20190919 MGI PMID:31240264 1557708 Ablim3 actin binding LIM protein family, member 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1557708 Ablim3 actin binding LIM protein family, member 3 gene MP:0001293 anophthalmia IEA N RGD:5509061 20220519 MGI 1557708 Ablim3 actin binding LIM protein family, member 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1557708 Ablim3 actin binding LIM protein family, member 3 gene MP:0002607 decreased basophil cell number IEA N RGD:5509061 20221215 MGI 1557708 Ablim3 actin binding LIM protein family, member 3 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20221215 MGI 1557708 Ablim3 actin binding LIM protein family, member 3 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1557709 Galp galanin-like peptide gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:18775887 1557709 Galp galanin-like peptide gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:18775887 1557709 Galp galanin-like peptide gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:18775887 1557710 Etfb electron transferring flavoprotein, beta polypeptide gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230601 MGI 1557710 Etfb electron transferring flavoprotein, beta polypeptide gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230601 MGI 1557710 Etfb electron transferring flavoprotein, beta polypeptide gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230601 MGI 1557710 Etfb electron transferring flavoprotein, beta polypeptide gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 1557710 Etfb electron transferring flavoprotein, beta polypeptide gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230601 MGI 1557710 Etfb electron transferring flavoprotein, beta polypeptide gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20240523 MGI 1557710 Etfb electron transferring flavoprotein, beta polypeptide gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1557713 Acot12 acyl-CoA thioesterase 12 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20230119 MGI 1557713 Acot12 acyl-CoA thioesterase 12 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20231026 MGI PMID:37150501 1557713 Acot12 acyl-CoA thioesterase 12 gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20240523 MGI 1557713 Acot12 acyl-CoA thioesterase 12 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20231026 MGI PMID:37150501 1557713 Acot12 acyl-CoA thioesterase 12 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20231026 MGI PMID:37150501 1557713 Acot12 acyl-CoA thioesterase 12 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20231026 MGI PMID:37150501 1557713 Acot12 acyl-CoA thioesterase 12 gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20231026 MGI PMID:37150501 1557713 Acot12 acyl-CoA thioesterase 12 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20231026 MGI PMID:37150501 1557713 Acot12 acyl-CoA thioesterase 12 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20231026 MGI PMID:37150501 1557713 Acot12 acyl-CoA thioesterase 12 gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20240523 MGI 1557713 Acot12 acyl-CoA thioesterase 12 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20231026 MGI PMID:37150501 1557713 Acot12 acyl-CoA thioesterase 12 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20231026 MGI PMID:37150501 1557713 Acot12 acyl-CoA thioesterase 12 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20231026 MGI PMID:37150501 1557715 Tle6 transducin-like enhancer of split 6 gene MP:0001926 female infertility IAGP N RGD:5509061 20200423 MGI PMID:25208553 1557715 Tle6 transducin-like enhancer of split 6 gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20200423 MGI PMID:25208553 1557715 Tle6 transducin-like enhancer of split 6 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20200423 MGI PMID:25208553 1557715 Tle6 transducin-like enhancer of split 6 gene MP:0020850 abnormal microtubule cytoskeleton morphology IAGP N RGD:5509061 20200423 MGI PMID:25208553 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7908720 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:7908720 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:7555717 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:7908720 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0000690 absent spleen IAGP N RGD:5509061 20151112 MGI PMID:25283275 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:18400903 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12023301 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12023301 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7908720 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:18400903 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0009322 increased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:7555717 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0009323 abnormal spleen development IAGP N RGD:5509061 20141003 MGI PMID:7555717 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0009323 abnormal spleen development IAGP N RGD:5509061 20141003 MGI PMID:7908720 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0010178 increased number of Howell-Jolly bodies IAGP N RGD:5509061 20141003 MGI PMID:7908720 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0011263 abnormal spleen mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:7908720 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0021091 abnormal dorsal interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:12023301 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0021093 abnormal dorsal interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:12023301 1557716 Tlx1 T cell leukemia, homeobox 1 gene MP:0021095 abnormal dorsal interneuron 4 morphology IAGP N RGD:5509061 20220310 MGI PMID:12023301 1557719 Tubb4b tubulin, beta 4B class IVB gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1557719 Tubb4b tubulin, beta 4B class IVB gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 1557719 Tubb4b tubulin, beta 4B class IVB gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20240229 MGI PMID:38031972 1557719 Tubb4b tubulin, beta 4B class IVB gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20240229 MGI PMID:38031972 1557719 Tubb4b tubulin, beta 4B class IVB gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20240229 MGI PMID:38031972 1557719 Tubb4b tubulin, beta 4B class IVB gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20240229 MGI PMID:38031972 1557719 Tubb4b tubulin, beta 4B class IVB gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20240229 MGI PMID:38031972 1557719 Tubb4b tubulin, beta 4B class IVB gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557719 Tubb4b tubulin, beta 4B class IVB gene MP:0011644 abnormal oviduct epithelium motile cilium morphology IAGP N RGD:5509061 20240229 MGI PMID:38031972 1557720 Cfp complement factor properdin gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:22308431 1557720 Cfp complement factor properdin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17916747 1557720 Cfp complement factor properdin gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:17916747 1557720 Cfp complement factor properdin gene MP:0002472 impaired complement alternative pathway IAGP N RGD:5509061 20141003 MGI PMID:17916747 1557720 Cfp complement factor properdin gene MP:0002472 impaired complement alternative pathway IAGP N RGD:5509061 20141003 MGI PMID:20941861 1557720 Cfp complement factor properdin gene MP:0002473 impaired complement classical pathway IAGP N RGD:5509061 20141003 MGI PMID:17916747 1557720 Cfp complement factor properdin gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20941861 1557720 Cfp complement factor properdin gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:18292556 1557720 Cfp complement factor properdin gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22308431 1557720 Cfp complement factor properdin gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18292556 1557721 Pbrm1 polybromo 1 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15601824 1557721 Pbrm1 polybromo 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:15601824 1557721 Pbrm1 polybromo 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:15601824 1557721 Pbrm1 polybromo 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 1557721 Pbrm1 polybromo 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:15601824 1557721 Pbrm1 polybromo 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1557721 Pbrm1 polybromo 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20181227 MGI 1557721 Pbrm1 polybromo 1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:15601824 1557721 Pbrm1 polybromo 1 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15601824 1557721 Pbrm1 polybromo 1 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15601824 1557721 Pbrm1 polybromo 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20161201 MGI PMID:22336179 1557721 Pbrm1 polybromo 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1557721 Pbrm1 polybromo 1 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20161201 MGI PMID:22336179 1557721 Pbrm1 polybromo 1 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20161201 MGI PMID:22336179 1557721 Pbrm1 polybromo 1 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20161201 MGI PMID:22336179 1557721 Pbrm1 polybromo 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1557721 Pbrm1 polybromo 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15601824 1557721 Pbrm1 polybromo 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557722 Galnt4 polypeptide N-acetylgalactosaminyltransferase 4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1557723 Sumo3 small ubiquitin-like modifier 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151112 MGI PMID:24891386 1557723 Sumo3 small ubiquitin-like modifier 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151112 MGI PMID:24891386 1557723 Sumo3 small ubiquitin-like modifier 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20151112 MGI PMID:24891386 1557723 Sumo3 small ubiquitin-like modifier 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20151112 MGI PMID:24891386 1557724 Trim62 tripartite motif-containing 62 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141127 MGI PMID:23838884 1557724 Trim62 tripartite motif-containing 62 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141127 MGI PMID:23838884 1557724 Trim62 tripartite motif-containing 62 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141127 MGI PMID:23838884 1557724 Trim62 tripartite motif-containing 62 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141127 MGI PMID:23838884 1557724 Trim62 tripartite motif-containing 62 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141127 MGI PMID:23838884 1557724 Trim62 tripartite motif-containing 62 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141127 MGI PMID:23838884 1557724 Trim62 tripartite motif-containing 62 gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141127 MGI PMID:23838884 1557724 Trim62 tripartite motif-containing 62 gene MP:0009591 increased liver adenocarcinoma incidence IAGP N RGD:5509061 20141127 MGI PMID:23838884 1557724 Trim62 tripartite motif-containing 62 gene MP:0010367 increased spindle cell carcinoma incidence IAGP N RGD:5509061 20141127 MGI PMID:23838884 1557724 Trim62 tripartite motif-containing 62 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141127 MGI PMID:23838884 1557725 Itga2b integrin alpha 2b gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:23935982 1557725 Itga2b integrin alpha 2b gene MP:0000440 domed cranium IEA N RGD:5509061 20200604 MGI 1557725 Itga2b integrin alpha 2b gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10942384 1557725 Itga2b integrin alpha 2b gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10942384 1557725 Itga2b integrin alpha 2b gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12871637 1557725 Itga2b integrin alpha 2b gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10942384 1557725 Itga2b integrin alpha 2b gene MP:0001891 hydrocephaly IEA N RGD:5509061 20200604 MGI 1557725 Itga2b integrin alpha 2b gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10942384 1557725 Itga2b integrin alpha 2b gene MP:0002083 premature death IEA N RGD:5509061 20200604 MGI 1557725 Itga2b integrin alpha 2b gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12871637 1557725 Itga2b integrin alpha 2b gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23935982 1557725 Itga2b integrin alpha 2b gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:10942384 1557725 Itga2b integrin alpha 2b gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10942384 1557725 Itga2b integrin alpha 2b gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12871637 1557725 Itga2b integrin alpha 2b gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17309829 1557725 Itga2b integrin alpha 2b gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12871637 1557725 Itga2b integrin alpha 2b gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:12871637 1557725 Itga2b integrin alpha 2b gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:12871637 1557725 Itga2b integrin alpha 2b gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:10942384 1557725 Itga2b integrin alpha 2b gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:12871637 1557725 Itga2b integrin alpha 2b gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:10942384 1557725 Itga2b integrin alpha 2b gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:10942384 1557725 Itga2b integrin alpha 2b gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:17309829 1557725 Itga2b integrin alpha 2b gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23935982 1557725 Itga2b integrin alpha 2b gene MP:0009548 abnormal platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:10942384 1557725 Itga2b integrin alpha 2b gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:10942384 1557725 Itga2b integrin alpha 2b gene MP:0009676 abnormal hemostasis IAGP N RGD:5509061 20141003 MGI PMID:10942384 1557725 Itga2b integrin alpha 2b gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20200604 MGI 1557725 Itga2b integrin alpha 2b gene MP:0011380 enlarged brain ventricles IEA N RGD:5509061 20200604 MGI 1557725 Itga2b integrin alpha 2b gene MP:0014060 abnormal platelet alpha-granule morphology IAGP N RGD:5509061 20170803 MGI PMID:10942384 1557725 Itga2b integrin alpha 2b gene MP:0031152 subcutaneous hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:10942384 1557726 Efhd1 EF hand domain containing 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20210603 MGI PMID:32414840 1557726 Efhd1 EF hand domain containing 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20210603 MGI PMID:32414840 1557726 Efhd1 EF hand domain containing 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20210603 MGI PMID:32414840 1557726 Efhd1 EF hand domain containing 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20210603 MGI PMID:32414840 1557726 Efhd1 EF hand domain containing 1 gene MP:0010055 abnormal sensory neuron physiology IAGP N RGD:5509061 20210603 MGI PMID:32414840 1557728 Tex11 testis expressed gene 11 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18369460 1557728 Tex11 testis expressed gene 11 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18316482 1557728 Tex11 testis expressed gene 11 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18316482 1557728 Tex11 testis expressed gene 11 gene MP:0004218 meiotic nondisjunction during M1 phase IAGP N RGD:5509061 20141003 MGI PMID:18316482 1557728 Tex11 testis expressed gene 11 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18316482 1557728 Tex11 testis expressed gene 11 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18369460 1557728 Tex11 testis expressed gene 11 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18316482 1557728 Tex11 testis expressed gene 11 gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20141003 MGI PMID:18316482 1557728 Tex11 testis expressed gene 11 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:18316482 1557729 Map4 microtubule-associated protein 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9626500 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0000440 domed cranium IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0002083 premature death IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0006062 abnormal vena cava morphology IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0008933 abnormal motile primary cilium physiology IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0011649 immotile respiratory cilia IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0013858 abnormal azygos vein topology IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557730 Dnaaf11 dynein axonemal assembly factor 11 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20190418 MGI PMID:27353389 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10574770 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:10574770 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:10574770 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0000542 left-sided isomerism IEA N RGD:5509061 20141003 MGI 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:10574770 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0000650 mesocardia IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:10574770 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10574770 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0003342 accessory spleen IEA N RGD:5509061 20141003 MGI 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:10574770 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0004113 abnormal aortic arch morphology IEA N RGD:5509061 20141003 MGI 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20141003 MGI 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141003 MGI PMID:10574770 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:10574770 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:10574770 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20141003 MGI 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0010422 heart right ventricle hypoplasia IEA N RGD:5509061 20141003 MGI 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0010426 abnormal heart and great artery attachment IAGP N RGD:5509061 20141003 MGI PMID:10574770 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0010443 total anomalous pulmonary venous connection, intracardiac IEA N RGD:5509061 20141003 MGI 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:10574770 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0010466 vascular ring IEA N RGD:5509061 20141003 MGI 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0010487 abnormal right subclavian artery morphology IEA N RGD:5509061 20141003 MGI 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:10574770 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10574770 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0011254 superior-inferior ventricles IEA N RGD:5509061 20141003 MGI 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0011569 abnormal azygos vein morphology IAGP N RGD:5509061 20141003 MGI PMID:10521397 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0011665 d-loop transposition of the great arteries IEA N RGD:5509061 20141003 MGI 1557732 Cfc1 cryptic, EGF-CFC family member 1 gene MP:0011673 unbalanced complete common atrioventricular canal IEA N RGD:5509061 20210708 MGI 1557733 Srgap1 SLIT-ROBO Rho GTPase activating protein 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20230323 MGI PMID:33514561 1557733 Srgap1 SLIT-ROBO Rho GTPase activating protein 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20230323 MGI PMID:33514561 1557733 Srgap1 SLIT-ROBO Rho GTPase activating protein 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20230323 MGI PMID:33514561 1557733 Srgap1 SLIT-ROBO Rho GTPase activating protein 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20230323 MGI PMID:33514561 1557733 Srgap1 SLIT-ROBO Rho GTPase activating protein 1 gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20230323 MGI PMID:33514561 1557733 Srgap1 SLIT-ROBO Rho GTPase activating protein 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20230323 MGI PMID:33514561 1557733 Srgap1 SLIT-ROBO Rho GTPase activating protein 1 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20230323 MGI PMID:33514561 1557733 Srgap1 SLIT-ROBO Rho GTPase activating protein 1 gene MP:0011402 renal cast IAGP N RGD:5509061 20230323 MGI PMID:33514561 1557733 Srgap1 SLIT-ROBO Rho GTPase activating protein 1 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20230323 MGI PMID:33514561 1557733 Srgap1 SLIT-ROBO Rho GTPase activating protein 1 gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20230323 MGI PMID:33514561 1557733 Srgap1 SLIT-ROBO Rho GTPase activating protein 1 gene MP:0011856 abnormal glomerular filtration barrier function IAGP N RGD:5509061 20230323 MGI PMID:33514561 1557733 Srgap1 SLIT-ROBO Rho GTPase activating protein 1 gene MP:0011869 detached podocyte IAGP N RGD:5509061 20230323 MGI PMID:33514561 1557735 Stradb STE20-related kinase adaptor beta gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1557735 Stradb STE20-related kinase adaptor beta gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1557736 Pyy peptide YY gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16680491 1557736 Pyy peptide YY gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:16950139 1557736 Pyy peptide YY gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22792209 1557736 Pyy peptide YY gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17920065 1557736 Pyy peptide YY gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:16680491 1557736 Pyy peptide YY gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16680491 1557736 Pyy peptide YY gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:16950139 1557736 Pyy peptide YY gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:16950139 1557736 Pyy peptide YY gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16680491 1557736 Pyy peptide YY gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15870288 1557736 Pyy peptide YY gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16950139 1557736 Pyy peptide YY gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:16680491 1557736 Pyy peptide YY gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:22792209 1557736 Pyy peptide YY gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17920065 1557736 Pyy peptide YY gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:22792209 1557736 Pyy peptide YY gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:16680491 1557736 Pyy peptide YY gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:16950139 1557736 Pyy peptide YY gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22792209 1557736 Pyy peptide YY gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:16680491 1557736 Pyy peptide YY gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17920065 1557736 Pyy peptide YY gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:17920065 1557736 Pyy peptide YY gene MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:16680491 1557736 Pyy peptide YY gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16680491 1557736 Pyy peptide YY gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:17920065 1557736 Pyy peptide YY gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17920065 1557736 Pyy peptide YY gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20141003 MGI PMID:16680491 1557736 Pyy peptide YY gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16950139 1557736 Pyy peptide YY gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16680491 1557736 Pyy peptide YY gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16680491 1557736 Pyy peptide YY gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16950139 1557736 Pyy peptide YY gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16680491 1557736 Pyy peptide YY gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:22792209 1557736 Pyy peptide YY gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:17920065 1557736 Pyy peptide YY gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:22792209 1557736 Pyy peptide YY gene MP:0021191 increased bone mineral density of lumbar vertebrae IAGP N RGD:5509061 20220922 MGI PMID:22792209 1557737 Tssk6 testis-specific serine kinase 6 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15870294 1557737 Tssk6 testis-specific serine kinase 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15870294 1557737 Tssk6 testis-specific serine kinase 6 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15870294 1557737 Tssk6 testis-specific serine kinase 6 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15870294 1557737 Tssk6 testis-specific serine kinase 6 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:15870294 1557740 Cd70 CD70 antigen gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:23269247 1557740 Cd70 CD70 antigen gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23269247 1557740 Cd70 CD70 antigen gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23269247 1557740 Cd70 CD70 antigen gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23547099 1557740 Cd70 CD70 antigen gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23269247 1557740 Cd70 CD70 antigen gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:23269247 1557741 Herc6 hect domain and RLD 6 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1557741 Herc6 hect domain and RLD 6 gene MP:0002997 enlarged seminal vesicle IAGP N RGD:5509061 20221124 MGI PMID:25406959 1557741 Herc6 hect domain and RLD 6 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1557741 Herc6 hect domain and RLD 6 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1557741 Herc6 hect domain and RLD 6 gene MP:0013899 abnormal seminal vesicle epithelium morphology IAGP N RGD:5509061 20221124 MGI PMID:25406959 1557742 Phf14 PHD finger protein 14 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22730381 1557742 Phf14 PHD finger protein 14 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 1557742 Phf14 PHD finger protein 14 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210520 MGI 1557742 Phf14 PHD finger protein 14 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210520 MGI 1557742 Phf14 PHD finger protein 14 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:22730381 1557742 Phf14 PHD finger protein 14 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:22730381 1557742 Phf14 PHD finger protein 14 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22730381 1557742 Phf14 PHD finger protein 14 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20210520 MGI 1557742 Phf14 PHD finger protein 14 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 1557742 Phf14 PHD finger protein 14 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:22730381 1557742 Phf14 PHD finger protein 14 gene MP:0010903 abnormal pulmonary alveolus wall morphology IAGP N RGD:5509061 20141003 MGI PMID:22730381 1557742 Phf14 PHD finger protein 14 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22730381 1557742 Phf14 PHD finger protein 14 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1557742 Phf14 PHD finger protein 14 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22730381 1557744 Trim35 tripartite motif-containing 35 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1557744 Trim35 tripartite motif-containing 35 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20210408 MGI PMID:32562145 1557744 Trim35 tripartite motif-containing 35 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210826 MGI 1557744 Trim35 tripartite motif-containing 35 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20210408 MGI PMID:32562145 1557744 Trim35 tripartite motif-containing 35 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210520 MGI 1557744 Trim35 tripartite motif-containing 35 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20210408 MGI PMID:32562145 1557744 Trim35 tripartite motif-containing 35 gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20210408 MGI PMID:32562145 1557746 Pde4c phosphodiesterase 4C, cAMP specific gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1557746 Pde4c phosphodiesterase 4C, cAMP specific gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1557747 Myoz1 myozenin 1 gene MP:0000562 polydactyly IEA N RGD:5509061 20160804 MGI 1557747 Myoz1 myozenin 1 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:18846255 1557747 Myoz1 myozenin 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:18846255 1557747 Myoz1 myozenin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18846255 1557747 Myoz1 myozenin 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:18846255 1557747 Myoz1 myozenin 1 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20201022 MGI 1557747 Myoz1 myozenin 1 gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20141003 MGI PMID:18846255 1557747 Myoz1 myozenin 1 gene MP:0003959 abnormal lean body mass IEA N RGD:5509061 20230601 MGI 1557747 Myoz1 myozenin 1 gene MP:0004142 abnormal muscle tone IAGP N RGD:5509061 20141003 MGI PMID:18846255 1557747 Myoz1 myozenin 1 gene MP:0004651 increased thoracic vertebrae number IEA N RGD:5509061 20160804 MGI 1557747 Myoz1 myozenin 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20201022 MGI 1557747 Myoz1 myozenin 1 gene MP:0008181 increased marginal zone B cell number IEA N RGD:5509061 20210520 MGI 1557747 Myoz1 myozenin 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20201022 MGI 1557747 Myoz1 myozenin 1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:18846255 1557747 Myoz1 myozenin 1 gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:18846255 1557747 Myoz1 myozenin 1 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:18846255 1557747 Myoz1 myozenin 1 gene MP:0009422 decreased gastrocnemius weight IAGP N RGD:5509061 20141003 MGI PMID:18846255 1557747 Myoz1 myozenin 1 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20201022 MGI 1557747 Myoz1 myozenin 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 1557747 Myoz1 myozenin 1 gene MP:0010100 increased cervical vertebrae number IEA N RGD:5509061 20160804 MGI 1557747 Myoz1 myozenin 1 gene MP:0012107 enhanced exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:18846255 1557747 Myoz1 myozenin 1 gene MP:0012320 abnormal body fat mass IEA N RGD:5509061 20230601 MGI 1557747 Myoz1 myozenin 1 gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:18846255 1557748 Tlr12 toll-like receptor 12 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15001781 1557748 Tlr12 toll-like receptor 12 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15001781 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:16410414 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20190418 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000344 absent Cajal-Retzius cell IAGP N RGD:5509061 20141003 MGI PMID:16410414 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20161013 MGI PMID:26290337 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:22101327 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20190912 MGI PMID:31197172 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20200102 MGI PMID:27618312 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20200402 MGI PMID:30093551 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17426285 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:23178126 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20151126 MGI PMID:24771530 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20161013 MGI PMID:26290337 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20170601 MGI PMID:26795843 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200102 MGI PMID:27618312 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:18702697 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:8812118 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:17901218 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20170629 MGI PMID:25568313 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20230928 MGI PMID:35604347 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19820705 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20190912 MGI PMID:31197172 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:18702697 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:19820705 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141016 MGI PMID:22705452 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15115821 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15219872 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16410414 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17828260 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18202285 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19661288 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20667915 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23658188 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20150521 MGI PMID:24857653 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20190215 MGI PMID:28288114 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20200102 MGI PMID:27618312 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20200130 MGI PMID:31112699 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20230928 MGI PMID:35604347 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23643363 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20161208 MGI PMID:24614806 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20230928 MGI PMID:35604347 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12890780 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20180830 MGI PMID:29809135 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15115821 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15219872 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:19661288 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20150108 MGI PMID:24719109 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:22101327 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20141003 MGI PMID:20667915 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20141003 MGI PMID:22101327 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20200402 MGI PMID:30093551 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:19661288 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:18702697 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:19661288 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:24174665 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20161208 MGI PMID:24614806 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:15219872 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:20667915 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:19709628 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:19820705 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:15219872 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141016 MGI PMID:22705452 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10963597 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000860 abnormal primary somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12498788 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000860 abnormal primary somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17828260 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000860 abnormal primary somatosensory cortex morphology IAGP N RGD:5509061 20210107 MGI PMID:31715135 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000862 absent barrels in primary somatosensory cortex IAGP N RGD:5509061 20141003 MGI PMID:10963597 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000862 absent barrels in primary somatosensory cortex IAGP N RGD:5509061 20141003 MGI PMID:12498788 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:16436615 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:24930700 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20200102 MGI PMID:27618312 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:23922229 1557750 Emx1 empty spiracles homeobox 1 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12890780 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10963597 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12890780 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23359422 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230928 MGI PMID:35604347 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15219872 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23136427 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150122 MGI PMID:24448406 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20161013 MGI PMID:26290337 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170629 MGI PMID:25568313 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:12890780 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22726441 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20220721 MGI PMID:35314861 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20190215 MGI PMID:28288114 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20190418 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:15219872 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:17956903 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17956903 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22726441 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20210107 MGI PMID:31715135 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001401 jumpy IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:24784230 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190418 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:24784230 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141218 MGI PMID:24937429 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210107 MGI PMID:31715135 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17956903 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:17956903 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20220421 MGI PMID:26868444 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:23136427 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20171221 MGI PMID:28346493 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:16410414 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:12890780 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20170629 MGI PMID:25568313 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:22726441 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20220421 MGI PMID:26868444 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:22726441 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:23136427 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20171221 MGI PMID:28346493 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18524897 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:23136427 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15115821 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:19661288 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20170629 MGI PMID:25568313 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20210527 MGI PMID:32202496 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:17956903 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:10963597 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23359422 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20150122 MGI PMID:24448406 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210527 MGI PMID:32202496 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141016 MGI PMID:22705452 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:20080609 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001909 reduced NMDA receptor mediated synaptic activity in barrel cortex IAGP N RGD:5509061 20141003 MGI PMID:10963597 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:12890780 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15219872 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20210107 MGI PMID:31715135 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15219872 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002064 seizures IAGP N RGD:5509061 20190418 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16410414 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12890780 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23922229 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24930700 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20150108 MGI PMID:24719109 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20190418 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20210527 MGI PMID:32202496 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:18579678 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:24930700 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10963597 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12151506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170126 MGI PMID:27693255 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20230928 MGI PMID:35604347 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20141218 MGI PMID:24937429 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20210527 MGI PMID:32202496 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:11027526 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:15219872 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:22284184 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:8812118 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20150122 MGI PMID:24448406 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:18702697 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:19661288 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141218 MGI PMID:24937429 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20150122 MGI PMID:24448406 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20190418 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20210527 MGI PMID:32202496 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20150108 MGI PMID:24719109 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:22726441 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20220421 MGI PMID:26868444 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20220721 MGI PMID:35314861 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002659 pituitary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17426285 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:19709628 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20190418 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20220721 MGI PMID:35314861 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:18487195 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:22678282 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20150219 MGI PMID:24623763 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18625319 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:23136427 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:15219872 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:17299771 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20180329 MGI PMID:28076783 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20080609 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:20080609 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:21321212 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20230928 MGI PMID:35604347 1557750 Emx1 empty spiracles homeobox 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:17901218 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:19661288 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22101327 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20150521 MGI PMID:24857653 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20230928 MGI PMID:35604347 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20150122 MGI PMID:24448406 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:19661288 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:19661288 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:23178126 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20190418 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:19661288 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21321212 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21452199 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20190418 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:22726441 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20220421 MGI PMID:26868444 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20150108 MGI PMID:24719109 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21185282 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201022 MGI 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141003 MGI PMID:17426285 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003817 abnormal pituitary diverticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:17426285 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003989 abnormal barrel cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17828260 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003989 abnormal barrel cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18524897 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003989 abnormal barrel cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18702697 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20190215 MGI PMID:28288114 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20220721 MGI PMID:35314861 1557750 Emx1 empty spiracles homeobox 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20150108 MGI PMID:24719109 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20161013 MGI PMID:26290337 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004164 abnormal neurohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:17426285 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004171 abnormal pallium development IAGP N RGD:5509061 20141003 MGI PMID:20667915 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004171 abnormal pallium development IAGP N RGD:5509061 20200402 MGI PMID:30093551 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18579678 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22101327 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20667915 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:23293287 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:19709628 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004495 decreased synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:23136427 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20080609 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20220721 MGI PMID:35314861 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:23658188 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20170629 MGI PMID:25568313 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:22101327 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:23643363 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20230928 MGI PMID:35604347 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21321212 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20190418 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004979 abnormal neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:23643363 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20150521 MGI PMID:24857653 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20200402 MGI PMID:30093551 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20230928 MGI PMID:35604347 1557750 Emx1 empty spiracles homeobox 1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20150108 MGI PMID:24719109 1557750 Emx1 empty spiracles homeobox 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:21321212 1557750 Emx1 empty spiracles homeobox 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0005267 abnormal olfactory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19820705 1557750 Emx1 empty spiracles homeobox 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20150108 MGI PMID:24719109 1557750 Emx1 empty spiracles homeobox 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22726441 1557750 Emx1 empty spiracles homeobox 1 gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20170629 MGI PMID:27939640 1557750 Emx1 empty spiracles homeobox 1 gene MP:0005655 increased aggression IAGP N RGD:5509061 20141003 MGI PMID:12890780 1557750 Emx1 empty spiracles homeobox 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:23658188 1557750 Emx1 empty spiracles homeobox 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20161208 MGI PMID:24614806 1557750 Emx1 empty spiracles homeobox 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20180329 MGI PMID:28076783 1557750 Emx1 empty spiracles homeobox 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:12890780 1557750 Emx1 empty spiracles homeobox 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23178126 1557750 Emx1 empty spiracles homeobox 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23643363 1557750 Emx1 empty spiracles homeobox 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20150122 MGI PMID:24448406 1557750 Emx1 empty spiracles homeobox 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20151126 MGI PMID:24771530 1557750 Emx1 empty spiracles homeobox 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20170601 MGI PMID:26795843 1557750 Emx1 empty spiracles homeobox 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20190215 MGI PMID:28288114 1557750 Emx1 empty spiracles homeobox 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557750 Emx1 empty spiracles homeobox 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20210527 MGI PMID:32202496 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008030 abnormal Cajal-Retzius cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21185282 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008030 abnormal Cajal-Retzius cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:18487195 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:24930700 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:23136427 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20210211 MGI PMID:33086056 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008222 decreased hippocampal commissure size IAGP N RGD:5509061 20141003 MGI PMID:18702697 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:15219872 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:22284184 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:18487195 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:18702697 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008262 abnormal hippocampus region morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008264 absent hippocampus CA1 region IAGP N RGD:5509061 20141003 MGI PMID:15219872 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008266 absent hippocampus CA2 region IAGP N RGD:5509061 20141003 MGI PMID:15219872 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008268 absent hippocampus CA3 region IAGP N RGD:5509061 20141003 MGI PMID:15219872 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:18702697 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:20667915 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20150122 MGI PMID:24448406 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20150521 MGI PMID:24857653 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:18702697 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008328 increased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:17426285 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008367 absent pituitary intermediate lobe IAGP N RGD:5509061 20141003 MGI PMID:17426285 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:23136427 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:22726441 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20220421 MGI PMID:26868444 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:23293287 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20170629 MGI PMID:25568313 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:23293287 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15115821 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20150122 MGI PMID:24448406 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:17901218 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:19661288 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20150122 MGI PMID:24448406 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19820705 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21452199 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22101327 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23643363 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23922229 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20170629 MGI PMID:25568313 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20200102 MGI PMID:27618312 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20200130 MGI PMID:31112699 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:24174665 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18702697 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:23643363 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:19661288 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20230928 MGI PMID:35604347 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:16410414 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:18579678 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008946 abnormal neuron number IAGP N RGD:5509061 20141003 MGI PMID:23643363 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20200130 MGI PMID:31112699 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20190912 MGI PMID:31197172 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20200102 MGI PMID:27618312 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20200402 MGI PMID:30093551 1557750 Emx1 empty spiracles homeobox 1 gene MP:0008949 increased Cajal-Retzius cell number IAGP N RGD:5509061 20141003 MGI PMID:18579678 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009324 absent hippocampal fimbria IAGP N RGD:5509061 20141003 MGI PMID:20667915 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:23359422 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20161013 MGI PMID:25143599 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20190215 MGI PMID:28288114 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22726441 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20171221 MGI PMID:28346493 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009457 whorled hair IAGP N RGD:5509061 20141003 MGI PMID:19357712 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009463 abnormal pituitary infundibular stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:17426285 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009682 abnormal anterior corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:22284184 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:23658188 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:20335472 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:23136427 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18579678 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19709628 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:23293287 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:23643363 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20171221 MGI PMID:28346493 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24174665 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009946 abnormal olfactory bulb layer morphology IAGP N RGD:5509061 20150122 MGI PMID:24448406 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009954 abnormal mitral cell morphology IAGP N RGD:5509061 20150122 MGI PMID:24448406 1557750 Emx1 empty spiracles homeobox 1 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22726441 1557750 Emx1 empty spiracles homeobox 1 gene MP:0010011 ectopic hippocampus pyramidal cells IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557750 Emx1 empty spiracles homeobox 1 gene MP:0010014 hippocampus pyramidal cell degeneration IAGP N RGD:5509061 20190418 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1557750 Emx1 empty spiracles homeobox 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20399730 1557750 Emx1 empty spiracles homeobox 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1557750 Emx1 empty spiracles homeobox 1 gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20170629 MGI PMID:25568313 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20141016 MGI PMID:22705452 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23359422 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20150122 MGI PMID:24448406 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18702697 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20150108 MGI PMID:24719109 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170629 MGI PMID:25568313 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23293287 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170629 MGI PMID:25568313 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011150 abnormal hippocampus stratum oriens morphology IAGP N RGD:5509061 20190815 MGI PMID:29311744 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011396 abnormal sleep behavior IAGP N RGD:5509061 20210107 MGI PMID:31715135 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20230928 MGI PMID:35604347 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011724 ectopic cortical neuron IAGP N RGD:5509061 20141003 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011724 ectopic cortical neuron IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20170629 MGI PMID:25568313 1557750 Emx1 empty spiracles homeobox 1 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20200102 MGI PMID:27618312 1557750 Emx1 empty spiracles homeobox 1 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20230928 MGI PMID:35604347 1557750 Emx1 empty spiracles homeobox 1 gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20200102 MGI PMID:27618312 1557750 Emx1 empty spiracles homeobox 1 gene MP:0012204 abnormal neuronal stem cell physiology IAGP N RGD:5509061 20200130 MGI PMID:31112699 1557750 Emx1 empty spiracles homeobox 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20161013 MGI PMID:25143599 1557750 Emx1 empty spiracles homeobox 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20220421 MGI PMID:26868444 1557750 Emx1 empty spiracles homeobox 1 gene MP:0012349 increased susceptibility to induction of seizure by inducing agent IAGP N RGD:5509061 20180830 MGI PMID:7806216 1557750 Emx1 empty spiracles homeobox 1 gene MP:0012448 abnormal primary motor cortex morphology IAGP N RGD:5509061 20210107 MGI PMID:31715135 1557750 Emx1 empty spiracles homeobox 1 gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20190215 MGI PMID:28288114 1557750 Emx1 empty spiracles homeobox 1 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:15115821 1557750 Emx1 empty spiracles homeobox 1 gene MP:0012504 increased forebrain apoptosis IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0012556 increased cell death IAGP N RGD:5509061 20200402 MGI PMID:30093551 1557750 Emx1 empty spiracles homeobox 1 gene MP:0012683 absent telencephalon IAGP N RGD:5509061 20200102 MGI PMID:27618312 1557750 Emx1 empty spiracles homeobox 1 gene MP:0013227 small brain ventricles IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20161013 MGI PMID:26290337 1557750 Emx1 empty spiracles homeobox 1 gene MP:0014254 increased paired-pulse ratio IAGP N RGD:5509061 20230706 MGI PMID:23136427 1557750 Emx1 empty spiracles homeobox 1 gene MP:0014372 decreased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:18524897 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020067 increased neocortex size IAGP N RGD:5509061 20150101 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020069 decreased neocortex size IAGP N RGD:5509061 20161103 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020069 decreased neocortex size IAGP N RGD:5509061 20170629 MGI PMID:25568313 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020069 decreased neocortex size IAGP N RGD:5509061 20200102 MGI PMID:27618312 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020069 decreased neocortex size IAGP N RGD:5509061 20210211 MGI PMID:33086056 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020337 abnormal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20190215 MGI PMID:28288114 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020379 abnormal sucrose solution preference IAGP N RGD:5509061 20220721 MGI PMID:35314861 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020388 decreased radial glial cell number IAGP N RGD:5509061 20161117 MGI PMID:21185282 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020388 decreased radial glial cell number IAGP N RGD:5509061 20161117 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020388 decreased radial glial cell number IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020388 decreased radial glial cell number IAGP N RGD:5509061 20200402 MGI PMID:30093551 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020389 increased radial glial cell number IAGP N RGD:5509061 20161117 MGI PMID:25100583 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020391 radial glial endfoot detachment IAGP N RGD:5509061 20161117 MGI PMID:21185282 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020392 abnormal radial glial cell apoptosis IAGP N RGD:5509061 20161117 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020393 increased neuronal precursor proliferation IAGP N RGD:5509061 20161117 MGI PMID:25948253 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20161117 MGI PMID:21185282 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20170518 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20170629 MGI PMID:25568313 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20220721 MGI PMID:35314861 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:14687546 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020536 increased subiculum size IAGP N RGD:5509061 20180301 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020594 decreased cerebral cortex cell number IAGP N RGD:5509061 20190215 MGI PMID:28288114 1557750 Emx1 empty spiracles homeobox 1 gene MP:0020912 abnormal susceptibility to Riboviria infection IAGP N RGD:5509061 20210211 MGI PMID:33086056 1557750 Emx1 empty spiracles homeobox 1 gene MP:0030004 hippocampus hypoplasia IAGP N RGD:5509061 20170706 MGI PMID:22266795 1557750 Emx1 empty spiracles homeobox 1 gene MP:0030707 decreased glutamine level IAGP N RGD:5509061 20190418 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0030733 decreased gamma-aminobutyric acid level IAGP N RGD:5509061 20190418 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0030737 decreased glutamic acid level IAGP N RGD:5509061 20190418 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0030743 decreased aspartic acid level IAGP N RGD:5509061 20190418 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0030955 abnormal Golgi trans cisterna morphology IAGP N RGD:5509061 20190725 MGI PMID:24174665 1557750 Emx1 empty spiracles homeobox 1 gene MP:0030956 abnormal neuronal precursor cell migration IAGP N RGD:5509061 20190725 MGI PMID:25757017 1557750 Emx1 empty spiracles homeobox 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:28288114 1557750 Emx1 empty spiracles homeobox 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:30053506 1557750 Emx1 empty spiracles homeobox 1 gene MP:0031392 hypoactivity IAGP N RGD:5509061 20220421 MGI PMID:26868444 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:20016100 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20160317 MGI PMID:25836420 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:20016100 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20160317 MGI PMID:25836420 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20160317 MGI PMID:25836420 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20141003 MGI PMID:19667187 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:20457918 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20160317 MGI PMID:25836420 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:20457918 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:21828077 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150806 MGI PMID:24427314 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:20064389 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21828077 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:21828077 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23270607 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20064389 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20190124 MGI PMID:27383589 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:21828077 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:20457918 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:20064389 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:20064389 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:19667187 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:20850369 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20160317 MGI PMID:25836420 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:21828077 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:20457918 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:20064389 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20211125 MGI PMID:34658337 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20211125 MGI PMID:34658337 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20457918 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20160317 MGI PMID:25836420 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21828077 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:20457918 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:23270607 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0005060 accumulation of giant lysosomes in kidney/renal tubule cells IAGP N RGD:5509061 20240718 MGI PMID:32375042 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:19667187 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19890007 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20160317 MGI PMID:25836420 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0006037 abnormal mitochondrial fission IAGP N RGD:5509061 20160317 MGI PMID:25836420 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21828077 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:23270607 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:20457918 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:19890007 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:20850369 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20240718 MGI PMID:32375042 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20141003 MGI PMID:20457918 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20141003 MGI PMID:21828077 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19667187 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:20064389 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19667187 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:19667187 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20190124 MGI PMID:27383589 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20160317 MGI PMID:25836420 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20016100 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0011267 abnormal excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:27383589 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20457918 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0011369 increased renal glomerulus apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20457918 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0011534 granular kidney IAGP N RGD:5509061 20141003 MGI PMID:20457918 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20160317 MGI PMID:25836420 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20160317 MGI PMID:25836420 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20160317 MGI PMID:25836420 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20160317 MGI PMID:25836420 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0014378 increased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:27383589 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0030949 abnormal Golgi vesicle transport IAGP N RGD:5509061 20240718 MGI PMID:32375042 1557751 Lrrk2 leucine-rich repeat kinase 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:25836420 1557752 Fabp12 fatty acid binding protein 12 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1557755 Ndufaf2 NADH:ubiquinone oxidoreductase complex assembly factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151119 MGI PMID:23702311 1557755 Ndufaf2 NADH:ubiquinone oxidoreductase complex assembly factor 2 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:23702311 1557757 Spmap2l sperm microtubule associated protein 2 like gene MP:0000745 tremors IEA N RGD:5509061 20231207 MGI 1557757 Spmap2l sperm microtubule associated protein 2 like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1557757 Spmap2l sperm microtubule associated protein 2 like gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20231207 MGI 1557758 Pot1a protection of telomeres 1A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16839876 1557758 Pot1a protection of telomeres 1A gene MP:0003155 abnormal telomere length IAGP N RGD:5509061 20141003 MGI PMID:16839876 1557758 Pot1a protection of telomeres 1A gene MP:0003701 elevated level of mitotic sister chromatid exchange IAGP N RGD:5509061 20141003 MGI PMID:16839876 1557758 Pot1a protection of telomeres 1A gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:16839876 1557758 Pot1a protection of telomeres 1A gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:16839876 1557758 Pot1a protection of telomeres 1A gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:16839877 1557758 Pot1a protection of telomeres 1A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16839876 1557758 Pot1a protection of telomeres 1A gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16839877 1557758 Pot1a protection of telomeres 1A gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16839877 1557759 Ube2l3 ubiquitin-conjugating enzyme E2L 3 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:8901595 1557759 Ube2l3 ubiquitin-conjugating enzyme E2L 3 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:8901595 1557759 Ube2l3 ubiquitin-conjugating enzyme E2L 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8901595 1557759 Ube2l3 ubiquitin-conjugating enzyme E2L 3 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:8901595 1557759 Ube2l3 ubiquitin-conjugating enzyme E2L 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8901595 1557759 Ube2l3 ubiquitin-conjugating enzyme E2L 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8901595 1557760 Vps9d1 VPS9 domain containing 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1557760 Vps9d1 VPS9 domain containing 1 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 1557763 Cyb5r3 cytochrome b5 reductase 3 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:31487266 1557763 Cyb5r3 cytochrome b5 reductase 3 gene MP:0001304 cataract IEA N RGD:5509061 20200310 MGI 1557763 Cyb5r3 cytochrome b5 reductase 3 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20200310 MGI PMID:31487266 1557763 Cyb5r3 cytochrome b5 reductase 3 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20200310 MGI PMID:31487266 1557763 Cyb5r3 cytochrome b5 reductase 3 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20200310 MGI PMID:31487266 1557763 Cyb5r3 cytochrome b5 reductase 3 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20200310 MGI PMID:31487266 1557763 Cyb5r3 cytochrome b5 reductase 3 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20200310 MGI PMID:31487266 1557763 Cyb5r3 cytochrome b5 reductase 3 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:31487266 1557763 Cyb5r3 cytochrome b5 reductase 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557763 Cyb5r3 cytochrome b5 reductase 3 gene MP:0012045 increased susceptibility to hypertension IAGP N RGD:5509061 20200310 MGI PMID:31487266 1557763 Cyb5r3 cytochrome b5 reductase 3 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1557764 Mthfs 5, 10-methenyltetrahydrofolate synthetase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:22303332 1557764 Mthfs 5, 10-methenyltetrahydrofolate synthetase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22303332 1557764 Mthfs 5, 10-methenyltetrahydrofolate synthetase gene MP:0011230 abnormal folic acid level IAGP N RGD:5509061 20141003 MGI PMID:22303332 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:17488636 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0000231 hypertension IAGP N RGD:5509061 20200521 MGI PMID:30765526 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:22550170 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:22550170 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0003017 decreased circulating bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:17488636 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0003017 decreased circulating bicarbonate level IAGP N RGD:5509061 20200521 MGI PMID:30765526 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20200521 MGI PMID:30765526 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:22550170 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20181115 MGI PMID:24655003 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0003028 alkalosis IAGP N RGD:5509061 20141003 MGI PMID:22550170 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0003029 alkalemia IAGP N RGD:5509061 20181115 MGI PMID:24655003 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0003031 acidosis IAGP N RGD:5509061 20141003 MGI PMID:17488636 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:22550170 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0003860 abnormal carbon dioxide level IAGP N RGD:5509061 20200521 MGI PMID:30765526 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0004119 hypokalemia IAGP N RGD:5509061 20141003 MGI PMID:22550170 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0005502 abnormal renal/urinary system physiology IAGP N RGD:5509061 20141003 MGI PMID:22550170 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:17488636 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20200521 MGI PMID:30765526 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:19633012 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:22550170 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20200521 MGI PMID:30765526 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:17488636 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20200521 MGI PMID:30765526 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0005634 decreased circulating sodium level IAGP N RGD:5509061 20181115 MGI PMID:24655003 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19633012 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20181115 MGI PMID:24655003 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0006274 abnormal urine sodium level IAGP N RGD:5509061 20200521 MGI PMID:30765526 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:19633012 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:22550170 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20200521 MGI PMID:30765526 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22550170 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22550170 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22550170 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:22550170 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:22550170 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0012339 hyperkalemia IAGP N RGD:5509061 20200521 MGI PMID:30765526 1557765 Wnk4 WNK lysine deficient protein kinase 4 gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20200521 MGI PMID:30765526 1557766 Gdpd2 glycerophosphodiester phosphodiesterase domain containing 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20201231 MGI PMID:31932351 1557766 Gdpd2 glycerophosphodiester phosphodiesterase domain containing 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20201231 MGI PMID:31932351 1557766 Gdpd2 glycerophosphodiester phosphodiesterase domain containing 2 gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20201231 MGI PMID:31932351 1557766 Gdpd2 glycerophosphodiester phosphodiesterase domain containing 2 gene MP:0010892 increased oligodendrocyte progenitor number IAGP N RGD:5509061 20201231 MGI PMID:31932351 1557766 Gdpd2 glycerophosphodiester phosphodiesterase domain containing 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1557766 Gdpd2 glycerophosphodiester phosphodiesterase domain containing 2 gene MP:0020393 increased neuronal precursor proliferation IAGP N RGD:5509061 20201231 MGI PMID:31932351 1557767 Myo7b myosin VIIB gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 1557767 Myo7b myosin VIIB gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1557767 Myo7b myosin VIIB gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160421 MGI 1557769 Mepce methylphosphate capping enzyme gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1557769 Mepce methylphosphate capping enzyme gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1557769 Mepce methylphosphate capping enzyme gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557769 Mepce methylphosphate capping enzyme gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1557770 Camp cathelicidin antimicrobial peptide gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23670560 1557770 Camp cathelicidin antimicrobial peptide gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:23670560 1557770 Camp cathelicidin antimicrobial peptide gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11719807 1557770 Camp cathelicidin antimicrobial peptide gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16751768 1557770 Camp cathelicidin antimicrobial peptide gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:23670560 1557770 Camp cathelicidin antimicrobial peptide gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23603910 1557770 Camp cathelicidin antimicrobial peptide gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16751768 1557770 Camp cathelicidin antimicrobial peptide gene MP:0011518 abnormal cell chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:23603910 1557771 Stk24 serine/threonine kinase 24 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20180614 MGI PMID:24176643 1557771 Stk24 serine/threonine kinase 24 gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20180614 MGI PMID:24176643 1557771 Stk24 serine/threonine kinase 24 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20180614 MGI PMID:24176643 1557771 Stk24 serine/threonine kinase 24 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20180614 MGI PMID:24176643 1557772 Irs4 insulin receptor substrate 4 gene MP:0001260 increased body weight IAGP N RGD:5509061 20160204 MGI PMID:24567904 1557772 Irs4 insulin receptor substrate 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10644546 1557772 Irs4 insulin receptor substrate 4 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:10644546 1557772 Irs4 insulin receptor substrate 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10644546 1557772 Irs4 insulin receptor substrate 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12502742 1557772 Irs4 insulin receptor substrate 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10644546 1557772 Irs4 insulin receptor substrate 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20160204 MGI PMID:24567904 1557772 Irs4 insulin receptor substrate 4 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12502742 1557772 Irs4 insulin receptor substrate 4 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160204 MGI PMID:24567904 1557772 Irs4 insulin receptor substrate 4 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:10644546 1557772 Irs4 insulin receptor substrate 4 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160204 MGI PMID:24567904 1557772 Irs4 insulin receptor substrate 4 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20160204 MGI PMID:24567904 1557772 Irs4 insulin receptor substrate 4 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:10644546 1557772 Irs4 insulin receptor substrate 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:10644546 1557772 Irs4 insulin receptor substrate 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12502742 1557772 Irs4 insulin receptor substrate 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20160204 MGI PMID:24567904 1557772 Irs4 insulin receptor substrate 4 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12502742 1557772 Irs4 insulin receptor substrate 4 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20160204 MGI PMID:24567904 1557772 Irs4 insulin receptor substrate 4 gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20160204 MGI PMID:24567904 1557772 Irs4 insulin receptor substrate 4 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20160204 MGI PMID:24567904 1557772 Irs4 insulin receptor substrate 4 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10644546 1557772 Irs4 insulin receptor substrate 4 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20160204 MGI PMID:24567904 1557772 Irs4 insulin receptor substrate 4 gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20160204 MGI PMID:24567904 1557772 Irs4 insulin receptor substrate 4 gene MP:0011939 increased food intake IAGP N RGD:5509061 20160204 MGI PMID:24567904 1557772 Irs4 insulin receptor substrate 4 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20160204 MGI PMID:24567904 1557772 Irs4 insulin receptor substrate 4 gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20160204 MGI PMID:24567904 1557773 Pnma3 paraneoplastic antigen MA3 gene MP:0008820 abnormal blood uric acid level IEA N RGD:5509061 20210520 MGI 1557774 Clec4g C-type lectin domain family 4, member g gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557774 Clec4g C-type lectin domain family 4, member g gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19632227 1557774 Clec4g C-type lectin domain family 4, member g gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:19632227 1557774 Clec4g C-type lectin domain family 4, member g gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:19632227 1557774 Clec4g C-type lectin domain family 4, member g gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:19632227 1557774 Clec4g C-type lectin domain family 4, member g gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19632227 1557774 Clec4g C-type lectin domain family 4, member g gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557774 Clec4g C-type lectin domain family 4, member g gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557774 Clec4g C-type lectin domain family 4, member g gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557774 Clec4g C-type lectin domain family 4, member g gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19632227 1557774 Clec4g C-type lectin domain family 4, member g gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19632227 1557774 Clec4g C-type lectin domain family 4, member g gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19632227 1557774 Clec4g C-type lectin domain family 4, member g gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23487419 1557774 Clec4g C-type lectin domain family 4, member g gene MP:0020932 decreased susceptibility to Adenoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:23487419 1557775 Cdc45 cell division cycle 45 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11416137 1557775 Cdc45 cell division cycle 45 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11416137 1557775 Cdc45 cell division cycle 45 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557775 Cdc45 cell division cycle 45 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:11416137 1557776 Dynlt2b dynein light chain Tctex-type 2B gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1557776 Dynlt2b dynein light chain Tctex-type 2B gene MP:0011940 decreased food intake IEA N RGD:5509061 20211021 MGI 1557777 Dock11 dedicator of cytokinesis 11 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1557777 Dock11 dedicator of cytokinesis 11 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20210429 MGI PMID:25729399 1557777 Dock11 dedicator of cytokinesis 11 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20220908 MGI PMID:32241915 1557777 Dock11 dedicator of cytokinesis 11 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 1557777 Dock11 dedicator of cytokinesis 11 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20210429 MGI PMID:25729399 1557777 Dock11 dedicator of cytokinesis 11 gene MP:0008241 abnormal metallophilic macrophage morphology IAGP N RGD:5509061 20210429 MGI PMID:25729399 1557777 Dock11 dedicator of cytokinesis 11 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20210429 MGI PMID:25729399 1557778 Pam16 presequence translocase-asssociated motor 16 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557778 Pam16 presequence translocase-asssociated motor 16 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1557778 Pam16 presequence translocase-asssociated motor 16 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1557779 Tceal3 transcription elongation factor A (SII)-like 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1557779 Tceal3 transcription elongation factor A (SII)-like 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1557779 Tceal3 transcription elongation factor A (SII)-like 3 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20181227 MGI 1557780 Clec9a C-type lectin domain family 9, member a gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:22209163 1557780 Clec9a C-type lectin domain family 9, member a gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:19219027 1557780 Clec9a C-type lectin domain family 9, member a gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20211021 MGI 1557781 Fkbp9 FK506 binding protein 9 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1557781 Fkbp9 FK506 binding protein 9 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160804 MGI 1557781 Fkbp9 FK506 binding protein 9 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 1557781 Fkbp9 FK506 binding protein 9 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20160804 MGI 1557783 En2 engrailed 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:7909289 1557783 En2 engrailed 2 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:12832534 1557783 En2 engrailed 2 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:1672471 1557783 En2 engrailed 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:7909289 1557783 En2 engrailed 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:8652061 1557783 En2 engrailed 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:1672471 1557783 En2 engrailed 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:7909289 1557783 En2 engrailed 2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:1672471 1557783 En2 engrailed 2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:7909289 1557783 En2 engrailed 2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:8652061 1557783 En2 engrailed 2 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:1672471 1557783 En2 engrailed 2 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0000865 absent cerebellum vermis IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0000867 abnormal cerebellum anterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0000868 decreased anterior vermis size IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0000869 abnormal cerebellum posterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0000869 abnormal cerebellum posterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0000869 abnormal cerebellum posterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:7909289 1557783 En2 engrailed 2 gene MP:0000869 abnormal cerebellum posterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:8652061 1557783 En2 engrailed 2 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:7909289 1557783 En2 engrailed 2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7909289 1557783 En2 engrailed 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0000900 decreased colliculi size IAGP N RGD:5509061 20141003 MGI PMID:7909289 1557783 En2 engrailed 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:16935268 1557783 En2 engrailed 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16935268 1557783 En2 engrailed 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17015829 1557783 En2 engrailed 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16935268 1557783 En2 engrailed 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:8652061 1557783 En2 engrailed 2 gene MP:0001440 abnormal grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:16935268 1557783 En2 engrailed 2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:16935268 1557783 En2 engrailed 2 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:16935268 1557783 En2 engrailed 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16935268 1557783 En2 engrailed 2 gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:16935268 1557783 En2 engrailed 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:16935268 1557783 En2 engrailed 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:16935268 1557783 En2 engrailed 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:16935268 1557783 En2 engrailed 2 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:16935268 1557783 En2 engrailed 2 gene MP:0002892 decreased superior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:17015829 1557783 En2 engrailed 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:8652061 1557783 En2 engrailed 2 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:16935268 1557783 En2 engrailed 2 gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20141003 MGI PMID:8652061 1557783 En2 engrailed 2 gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:17015829 1557783 En2 engrailed 2 gene MP:0004096 abnormal midbrain-hindbrain boundary development IAGP N RGD:5509061 20141003 MGI PMID:11124114 1557783 En2 engrailed 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17015829 1557783 En2 engrailed 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:8652061 1557783 En2 engrailed 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:17015829 1557783 En2 engrailed 2 gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0006105 small tectum IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0006106 absent tectum IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17015829 1557783 En2 engrailed 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0009039 absent inferior colliculus IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0009040 absent superior colliculus IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0009041 absent colliculi IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0009957 abnormal cerebellum vermis lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0009963 abnormal cerebellum hemisphere lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0009968 abnormal cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:17015829 1557783 En2 engrailed 2 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:16935268 1557783 En2 engrailed 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17015829 1557783 En2 engrailed 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20081196 1557783 En2 engrailed 2 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:17015829 1557783 En2 engrailed 2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:17015829 1557783 En2 engrailed 2 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:11124114 1557783 En2 engrailed 2 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20141003 MGI PMID:11124114 1557783 En2 engrailed 2 gene MP:0012785 decreased rhombomere 1 size IAGP N RGD:5509061 20141003 MGI PMID:11124114 1557783 En2 engrailed 2 gene MP:0012785 decreased rhombomere 1 size IAGP N RGD:5509061 20141003 MGI PMID:17537797 1557783 En2 engrailed 2 gene MP:0012787 absent rhombomere 1 IAGP N RGD:5509061 20141003 MGI PMID:11124114 1557784 Kcp kielin/chordin-like protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557784 Kcp kielin/chordin-like protein gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557784 Kcp kielin/chordin-like protein gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15793581 1557784 Kcp kielin/chordin-like protein gene MP:0003639 abnormal response to vitamins IAGP N RGD:5509061 20141003 MGI PMID:15793581 1557784 Kcp kielin/chordin-like protein gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557784 Kcp kielin/chordin-like protein gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557784 Kcp kielin/chordin-like protein gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15793581 1557784 Kcp kielin/chordin-like protein gene MP:0011376 abnormal kidney corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:17035289 1557785 Asb5 ankyrin repeat and SOCs box-containing 5 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20201231 MGI 1557785 Asb5 ankyrin repeat and SOCs box-containing 5 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20200514 MGI 1557785 Asb5 ankyrin repeat and SOCs box-containing 5 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20200514 MGI 1557785 Asb5 ankyrin repeat and SOCs box-containing 5 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20201022 MGI 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20210506 MGI PMID:27504012 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20210506 MGI PMID:27504012 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20210506 MGI PMID:27504012 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20190620 MGI PMID:30550785 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20210506 MGI PMID:27504012 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20210506 MGI PMID:30940158 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20190620 MGI PMID:30550785 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210506 MGI PMID:30940158 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20190620 MGI PMID:30550785 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0010932 increased trabecular bone connectivity density IAGP N RGD:5509061 20190620 MGI PMID:30550785 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0010953 abnormal fatty acid oxidation IAGP N RGD:5509061 20210506 MGI PMID:27504012 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0012072 decreased susceptibility to osteoporosis IAGP N RGD:5509061 20190620 MGI PMID:30550785 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0030484 abnormal osteocyte lacuna morphology IAGP N RGD:5509061 20190620 MGI PMID:30550785 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20210610 MGI PMID:27504012 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0031265 increased susceptibility to hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:27504012 1557788 Fndc5 fibronectin type III domain containing 5 gene MP:0031269 increased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:27504012 1557790 Nkap NFKB activating protein gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19409814 1557790 Nkap NFKB activating protein gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19409814 1557790 Nkap NFKB activating protein gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19409814 1557790 Nkap NFKB activating protein gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19409814 1557790 Nkap NFKB activating protein gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19409814 1557790 Nkap NFKB activating protein gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19409814 1557790 Nkap NFKB activating protein gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19409814 1557790 Nkap NFKB activating protein gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19409814 1557791 Lonrf3 LON peptidase N-terminal domain and ring finger 3 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 1557791 Lonrf3 LON peptidase N-terminal domain and ring finger 3 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20210128 MGI 1557791 Lonrf3 LON peptidase N-terminal domain and ring finger 3 gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20210128 MGI 1557793 Fpr2 formyl peptide receptor 2 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:23454745 1557793 Fpr2 formyl peptide receptor 2 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:23454745 1557793 Fpr2 formyl peptide receptor 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23454745 1557793 Fpr2 formyl peptide receptor 2 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23603910 1557793 Fpr2 formyl peptide receptor 2 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:20107188 1557793 Fpr2 formyl peptide receptor 2 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:23454745 1557793 Fpr2 formyl peptide receptor 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20107188 1557793 Fpr2 formyl peptide receptor 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20107188 1557793 Fpr2 formyl peptide receptor 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23454745 1557793 Fpr2 formyl peptide receptor 2 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:23454745 1557793 Fpr2 formyl peptide receptor 2 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:23454745 1557793 Fpr2 formyl peptide receptor 2 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:20107188 1557793 Fpr2 formyl peptide receptor 2 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:20107188 1557793 Fpr2 formyl peptide receptor 2 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23603910 1557793 Fpr2 formyl peptide receptor 2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:23454745 1557793 Fpr2 formyl peptide receptor 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23454745 1557793 Fpr2 formyl peptide receptor 2 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557793 Fpr2 formyl peptide receptor 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23454745 1557793 Fpr2 formyl peptide receptor 2 gene MP:0010740 abnormal dendritic cell chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:23603910 1557793 Fpr2 formyl peptide receptor 2 gene MP:0010862 decreased respiratory mucosa goblet cell number IAGP N RGD:5509061 20141003 MGI PMID:20200280 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20161201 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20161201 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20161201 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:12381721 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:16530751 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:12381721 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16530751 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001061 abnormal oculomotor nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16530751 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001063 abnormal trochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16530751 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12912906 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:19164181 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:23762465 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:12381721 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20161201 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20161201 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23762465 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20161201 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:23762465 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20161201 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:12381721 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12912906 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12912906 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12381721 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12381721 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20161201 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:12381721 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:12912906 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12912906 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0002824 abnormal chorioallantoic fusion IEA N RGD:5509061 20161201 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:12381721 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0002861 abnormal tail bud morphology IAGP N RGD:5509061 20141003 MGI PMID:12381721 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20161201 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20161201 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20161201 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20161201 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12381721 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:12381721 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:12912906 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:12912906 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20161201 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0008786 abnormal hindgut morphology IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:12912906 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0009010 abnormal diestrus IAGP N RGD:5509061 20141003 MGI PMID:12912906 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:12912906 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20141003 MGI PMID:12912906 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12381721 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:23762465 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19164181 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23762465 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12381721 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0012086 absent hindgut IAGP N RGD:5509061 20141003 MGI PMID:12381721 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0012544 abnormal caudal neuropore morphology IAGP N RGD:5509061 20141003 MGI PMID:11134352 1557794 Nr6a1 nuclear receptor subfamily 6, group A, member 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1557795 Zfp277 zinc finger protein 277 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20808772 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20570919 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20190912 MGI PMID:23704941 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20190912 MGI PMID:28129027 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20190912 MGI PMID:28129027 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230629 MGI PMID:33890822 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20190912 MGI PMID:24305829 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:20570919 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20230629 MGI PMID:33890822 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20190912 MGI PMID:23704941 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20230629 MGI PMID:33890822 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20160721 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20160721 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20160721 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20190912 MGI PMID:23704941 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20190912 MGI PMID:23704941 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20230629 MGI PMID:33890822 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20190912 MGI PMID:23704941 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20190912 MGI PMID:23704941 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20190912 MGI PMID:24305829 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20230629 MGI PMID:33890822 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20190912 MGI PMID:23704941 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20230629 MGI PMID:33890822 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20230629 MGI PMID:33890822 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20190912 MGI PMID:23704941 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0004857 abnormal heart weight IAGP N RGD:5509061 20141003 MGI PMID:20570919 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20190912 MGI PMID:23704941 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20190912 MGI PMID:23704941 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20160721 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20160721 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20160721 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20160721 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20190912 MGI PMID:23704941 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20160721 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:20570919 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20190912 MGI PMID:23704941 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20230629 MGI PMID:33890822 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0006376 decreased circulating angiotensinogen level IAGP N RGD:5509061 20230629 MGI PMID:33890822 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20160721 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20190912 MGI PMID:24305829 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20230629 MGI PMID:33890822 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0009349 increased urine pH IAGP N RGD:5509061 20190912 MGI PMID:23704941 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20160721 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20230629 MGI PMID:33890822 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20190912 MGI PMID:28129027 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20570919 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160721 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0011282 increased podocyte apoptosis IAGP N RGD:5509061 20160721 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20190912 MGI PMID:23704941 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0011351 absent proximal convoluted tubule brush border IAGP N RGD:5509061 20160721 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0011402 renal cast IAGP N RGD:5509061 20160915 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0011457 abnormal metanephric ureteric bud development IAGP N RGD:5509061 20190912 MGI PMID:23704941 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20230629 MGI PMID:33890822 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20190912 MGI PMID:24305829 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0012024 abnormal nephron morphogenesis IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0012025 abnormal comma shaped body morphology IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0012026 abnormal S-shaped body morphology IAGP N RGD:5509061 20190912 MGI PMID:26658320 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0012046 decreased susceptibility to hypertension IAGP N RGD:5509061 20230629 MGI PMID:33890822 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20190912 MGI PMID:24305829 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20190912 MGI PMID:24305829 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20161013 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:22034640 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190912 MGI PMID:28129027 1557796 Atp6ap2 ATPase, H+ transporting, lysosomal accessory protein 2 gene MP:0031358 decreased urine output IAGP N RGD:5509061 20230629 MGI PMID:33890822 1557797 Bcl6b B cell CLL/lymphoma 6, member B gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17526724 1557797 Bcl6b B cell CLL/lymphoma 6, member B gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17526724 1557797 Bcl6b B cell CLL/lymphoma 6, member B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17526724 1557797 Bcl6b B cell CLL/lymphoma 6, member B gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17526724 1557797 Bcl6b B cell CLL/lymphoma 6, member B gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:17526724 1557797 Bcl6b B cell CLL/lymphoma 6, member B gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15314041 1557797 Bcl6b B cell CLL/lymphoma 6, member B gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17526724 1557797 Bcl6b B cell CLL/lymphoma 6, member B gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15314041 1557797 Bcl6b B cell CLL/lymphoma 6, member B gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17526724 1557797 Bcl6b B cell CLL/lymphoma 6, member B gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:15833813 1557797 Bcl6b B cell CLL/lymphoma 6, member B gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15833813 1557797 Bcl6b B cell CLL/lymphoma 6, member B gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:15833813 1557798 Treml1 triggering receptor expressed on myeloid cells-like 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19436112 1557798 Treml1 triggering receptor expressed on myeloid cells-like 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19436112 1557798 Treml1 triggering receptor expressed on myeloid cells-like 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:19436112 1557798 Treml1 triggering receptor expressed on myeloid cells-like 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19436112 1557798 Treml1 triggering receptor expressed on myeloid cells-like 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:19436112 1557798 Treml1 triggering receptor expressed on myeloid cells-like 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:19436112 1557798 Treml1 triggering receptor expressed on myeloid cells-like 1 gene MP:0011514 skin hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19436112 1557798 Treml1 triggering receptor expressed on myeloid cells-like 1 gene MP:0031083 increased circulating D-dimer level IAGP N RGD:5509061 20200709 MGI PMID:19436112 1557802 Ldb3 LIM domain binding 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:21303826 1557802 Ldb3 LIM domain binding 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:19028670 1557802 Ldb3 LIM domain binding 3 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19028670 1557802 Ldb3 LIM domain binding 3 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19028670 1557802 Ldb3 LIM domain binding 3 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:11696561 1557802 Ldb3 LIM domain binding 3 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:11696561 1557802 Ldb3 LIM domain binding 3 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:12499364 1557802 Ldb3 LIM domain binding 3 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:11696561 1557802 Ldb3 LIM domain binding 3 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12499364 1557802 Ldb3 LIM domain binding 3 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20200402 MGI 1557802 Ldb3 LIM domain binding 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12499364 1557802 Ldb3 LIM domain binding 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21303826 1557802 Ldb3 LIM domain binding 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1557802 Ldb3 LIM domain binding 3 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:11696561 1557802 Ldb3 LIM domain binding 3 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:19028670 1557802 Ldb3 LIM domain binding 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11696561 1557802 Ldb3 LIM domain binding 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19028670 1557802 Ldb3 LIM domain binding 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21303826 1557802 Ldb3 LIM domain binding 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11696561 1557802 Ldb3 LIM domain binding 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19028670 1557802 Ldb3 LIM domain binding 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21303826 1557802 Ldb3 LIM domain binding 3 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1557802 Ldb3 LIM domain binding 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:11696561 1557802 Ldb3 LIM domain binding 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:19028670 1557802 Ldb3 LIM domain binding 3 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11696561 1557802 Ldb3 LIM domain binding 3 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:19028670 1557802 Ldb3 LIM domain binding 3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:19028670 1557802 Ldb3 LIM domain binding 3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:21303826 1557802 Ldb3 LIM domain binding 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19028670 1557802 Ldb3 LIM domain binding 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21303826 1557802 Ldb3 LIM domain binding 3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20200402 MGI 1557802 Ldb3 LIM domain binding 3 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12499364 1557802 Ldb3 LIM domain binding 3 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21303826 1557802 Ldb3 LIM domain binding 3 gene MP:0003158 dysphagia IAGP N RGD:5509061 20141003 MGI PMID:11696561 1557802 Ldb3 LIM domain binding 3 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20231109 MGI PMID:21303826 1557802 Ldb3 LIM domain binding 3 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19028670 1557802 Ldb3 LIM domain binding 3 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19028670 1557802 Ldb3 LIM domain binding 3 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:21303826 1557802 Ldb3 LIM domain binding 3 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:21303826 1557802 Ldb3 LIM domain binding 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21303826 1557802 Ldb3 LIM domain binding 3 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19028670 1557802 Ldb3 LIM domain binding 3 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11696561 1557802 Ldb3 LIM domain binding 3 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:12499364 1557802 Ldb3 LIM domain binding 3 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:12499364 1557802 Ldb3 LIM domain binding 3 gene MP:0010021 heart vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:11696561 1557802 Ldb3 LIM domain binding 3 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20210128 MGI 1557802 Ldb3 LIM domain binding 3 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:19028670 1557802 Ldb3 LIM domain binding 3 gene MP:0010563 increased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:21303826 1557802 Ldb3 LIM domain binding 3 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:21303826 1557802 Ldb3 LIM domain binding 3 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:19028670 1557802 Ldb3 LIM domain binding 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11696561 1557802 Ldb3 LIM domain binding 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12499364 1557802 Ldb3 LIM domain binding 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21303826 1557802 Ldb3 LIM domain binding 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11696561 1557802 Ldb3 LIM domain binding 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557802 Ldb3 LIM domain binding 3 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 1557802 Ldb3 LIM domain binding 3 gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:21303826 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210128 MGI 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0001705 abnormal proximal-distal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0005163 cyclopia IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0006290 proboscis IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0011192 decreased embryonic epiblast cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:20040491 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557804 Tgif2 TGFB-induced factor homeobox 2 gene MP:0012706 decreased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20160929 MGI PMID:22383895 1557806 Trnt1 tRNA nucleotidyl transferase, CCA-adding, 1 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1557806 Trnt1 tRNA nucleotidyl transferase, CCA-adding, 1 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20160804 MGI 1557806 Trnt1 tRNA nucleotidyl transferase, CCA-adding, 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 1557807 Plxna1 plexin A1 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17145500 1557807 Plxna1 plexin A1 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20170525 MGI PMID:26319580 1557807 Plxna1 plexin A1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16715077 1557807 Plxna1 plexin A1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20512151 1557807 Plxna1 plexin A1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16715077 1557807 Plxna1 plexin A1 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1557807 Plxna1 plexin A1 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1557807 Plxna1 plexin A1 gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1557807 Plxna1 plexin A1 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17145500 1557807 Plxna1 plexin A1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20512151 1557807 Plxna1 plexin A1 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1557807 Plxna1 plexin A1 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16715077 1557807 Plxna1 plexin A1 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1557807 Plxna1 plexin A1 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1557807 Plxna1 plexin A1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1557807 Plxna1 plexin A1 gene MP:0010197 abnormal lymphatic vessel endothelial cell morphology IAGP N RGD:5509061 20170525 MGI PMID:26319580 1557807 Plxna1 plexin A1 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:16715077 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0000433 microcephaly IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20191219 MGI PMID:30613052 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0001785 edema IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0004259 small placenta IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0004559 small allantois IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20230629 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0011257 abnormal head fold morphology IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20191219 MGI PMID:30613052 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20160616 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:27179789 1557808 Ddx3x DEAD box helicase 3, X-linked gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20191219 MGI PMID:27179789 1557809 Ero1b endoplasmic reticulum oxidoreductase 1 beta gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20308425 1557809 Ero1b endoplasmic reticulum oxidoreductase 1 beta gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20308425 1557809 Ero1b endoplasmic reticulum oxidoreductase 1 beta gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20308425 1557809 Ero1b endoplasmic reticulum oxidoreductase 1 beta gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20308425 1557809 Ero1b endoplasmic reticulum oxidoreductase 1 beta gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:20308425 1557809 Ero1b endoplasmic reticulum oxidoreductase 1 beta gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:20308425 1557811 Arl8b ADP-ribosylation factor-like 8B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180125 MGI PMID:28827407 1557811 Arl8b ADP-ribosylation factor-like 8B gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20180125 MGI PMID:28827407 1557811 Arl8b ADP-ribosylation factor-like 8B gene MP:0004264 abnormal extraembryonic tissue physiology IAGP N RGD:5509061 20180125 MGI PMID:28827407 1557811 Arl8b ADP-ribosylation factor-like 8B gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20201022 MGI 1557811 Arl8b ADP-ribosylation factor-like 8B gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20180125 MGI PMID:28827407 1557811 Arl8b ADP-ribosylation factor-like 8B gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1557811 Arl8b ADP-ribosylation factor-like 8B gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20180125 MGI PMID:28827407 1557811 Arl8b ADP-ribosylation factor-like 8B gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1557811 Arl8b ADP-ribosylation factor-like 8B gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180125 MGI PMID:28827407 1557811 Arl8b ADP-ribosylation factor-like 8B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20170105 MGI 1557811 Arl8b ADP-ribosylation factor-like 8B gene MP:0020515 abnormal visceral yolk sac endoderm morphology IAGP N RGD:5509061 20180125 MGI PMID:28827407 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0001214 skin hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0010344 increased hibernoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0013538 increased Harderian gland adenoma incidence IAGP N RGD:5509061 20150219 MGI PMID:21436583 1557812 Pinx1 PIN2/TERF1 interacting, telomerase inhibitor 1 gene MP:0030928 increased telomere length IAGP N RGD:5509061 20190117 MGI PMID:21436583 1557813 Edem1 ER degradation enhancer, mannosidase alpha-like 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1557813 Edem1 ER degradation enhancer, mannosidase alpha-like 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230601 MGI 1557813 Edem1 ER degradation enhancer, mannosidase alpha-like 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20240523 MGI 1557813 Edem1 ER degradation enhancer, mannosidase alpha-like 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20240523 MGI 1557813 Edem1 ER degradation enhancer, mannosidase alpha-like 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20240523 MGI 1557815 Nbas neuroblastoma amplified sequence gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 1557815 Nbas neuroblastoma amplified sequence gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1557815 Nbas neuroblastoma amplified sequence gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1557815 Nbas neuroblastoma amplified sequence gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20181227 MGI 1557815 Nbas neuroblastoma amplified sequence gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20181227 MGI 1557815 Nbas neuroblastoma amplified sequence gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20211021 MGI 1557815 Nbas neuroblastoma amplified sequence gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1557815 Nbas neuroblastoma amplified sequence gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0000747 muscle weakness IAGP N RGD:5509061 20240104 MGI PMID:37390204 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20240104 MGI PMID:37390204 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20111116 MGI 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0005369 muscle phenotype IAGP N RGD:5509061 20240104 MGI PMID:37390204 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0005376 homeostasis/metabolism phenotype IAGP N RGD:5509061 20240104 MGI PMID:37390204 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20240104 MGI PMID:37390204 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0005380 embryo phenotype IAGP N RGD:5509061 20240104 MGI PMID:37390204 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0005385 cardiovascular system phenotype IAGP N RGD:5509061 20240104 MGI PMID:37390204 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0005386 behavior/neurological phenotype IAGP N RGD:5509061 20240104 MGI PMID:37390204 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240104 MGI PMID:37390204 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20240104 MGI PMID:37390204 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20240104 MGI PMID:37390204 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20240104 MGI PMID:37390204 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20240104 MGI PMID:37390204 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20240104 MGI PMID:37390204 1557816 Npl N-acetylneuraminate pyruvate lyase gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20240104 MGI PMID:37390204 1557817 Mr1 major histocompatibility complex, class I-related gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20230119 MGI 1557817 Mr1 major histocompatibility complex, class I-related gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12634786 1557817 Mr1 major histocompatibility complex, class I-related gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16878136 1557817 Mr1 major histocompatibility complex, class I-related gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20230119 MGI 1557817 Mr1 major histocompatibility complex, class I-related gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:12634786 1557817 Mr1 major histocompatibility complex, class I-related gene MP:0020186 abnormal susceptibility to bacterial infection IAGP N RGD:5509061 20200416 MGI PMID:31113973 1557821 Zftraf1 zinc finger TRAF type containing 1 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20230601 MGI 1557821 Zftraf1 zinc finger TRAF type containing 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1557821 Zftraf1 zinc finger TRAF type containing 1 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20230601 MGI 1557822 Slco6d1 solute carrier organic anion transporter family, member 6d1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210128 MGI 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:11585928 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0001460 abnormal olfactory discrimination memory IAGP N RGD:5509061 20141003 MGI PMID:11481456 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11585928 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18043734 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11585928 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:11481456 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:11585928 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11585928 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:11585928 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:11585928 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:11585928 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0009234 absent sperm head IAGP N RGD:5509061 20141003 MGI PMID:11585928 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:11585928 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20141003 MGI PMID:11585928 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20141003 MGI PMID:11585928 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0013716 hypolactation IAGP N RGD:5509061 20150611 MGI PMID:11585928 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20180621 MGI PMID:11585928 1557823 Neurl1a neuralized E3 ubiquitin protein ligase 1A gene MP:0031410 biflagellated sperm IAGP N RGD:5509061 20220630 MGI PMID:11585928 1557825 Slc52a2 solute carrier protein 52, member 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20160811 MGI 1557825 Slc52a2 solute carrier protein 52, member 2 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20160421 MGI 1557825 Slc52a2 solute carrier protein 52, member 2 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20160811 MGI 1557825 Slc52a2 solute carrier protein 52, member 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1557825 Slc52a2 solute carrier protein 52, member 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20211028 MGI PMID:33518683 1557825 Slc52a2 solute carrier protein 52, member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1557826 Sms spermine synthase gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23870131 1557826 Sms spermine synthase gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557826 Sms spermine synthase gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:23870131 1557826 Sms spermine synthase gene MP:0000162 lordosis IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557826 Sms spermine synthase gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:23870131 1557826 Sms spermine synthase gene MP:0001258 decreased body length IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557826 Sms spermine synthase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557826 Sms spermine synthase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23870131 1557826 Sms spermine synthase gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557826 Sms spermine synthase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23870131 1557826 Sms spermine synthase gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557826 Sms spermine synthase gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557826 Sms spermine synthase gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23870131 1557826 Sms spermine synthase gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557826 Sms spermine synthase gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557826 Sms spermine synthase gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160804 MGI 1557826 Sms spermine synthase gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20160804 MGI 1557826 Sms spermine synthase gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20160804 MGI 1557826 Sms spermine synthase gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557826 Sms spermine synthase gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557826 Sms spermine synthase gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557826 Sms spermine synthase gene MP:0013600 testis degeneration IAGP N RGD:5509061 20160922 MGI PMID:24652767 1557827 Ano7 anoctamin 7 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20181227 MGI 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0000929 open neural tube IEA N RGD:5509061 20111116 MGI 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0001147 small testis IAGP N RGD:5509061 20220630 MGI PMID:28559472 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220630 MGI PMID:28559472 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0001698 decreased embryo size IEA N RGD:5509061 20141003 MGI 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0001925 male infertility IAGP N RGD:5509061 20220630 MGI PMID:28559472 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220630 MGI PMID:28559472 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:22699621 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22699621 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220630 MGI PMID:28559472 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220630 MGI PMID:28559472 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0003752 increased oral papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:22699621 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0004180 failure of initiation of embryo turning IEA N RGD:5509061 20111116 MGI 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20220630 MGI PMID:28559472 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0004251 failure of heart looping IEA N RGD:5509061 20111116 MGI 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220630 MGI PMID:28559472 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220630 MGI PMID:28559472 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220630 MGI PMID:28559472 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22699621 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22699621 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0009657 failure of chorioallantoic fusion IEA N RGD:5509061 20111116 MGI 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0012105 delayed gastrulation IEA N RGD:5509061 20141003 MGI 1557828 Usp9x ubiquitin specific peptidase 9, X chromosome gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220630 MGI PMID:28559472 1557829 Pmm2 phosphomannomutase 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20160811 MGI 1557829 Pmm2 phosphomannomutase 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22157680 1557829 Pmm2 phosphomannomutase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22157680 1557829 Pmm2 phosphomannomutase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:22157680 1557829 Pmm2 phosphomannomutase 2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:22157680 1557829 Pmm2 phosphomannomutase 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22157680 1557829 Pmm2 phosphomannomutase 2 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:16847317 1557829 Pmm2 phosphomannomutase 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22157680 1557829 Pmm2 phosphomannomutase 2 gene MP:0004144 hypotonia IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22157680 1557829 Pmm2 phosphomannomutase 2 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22157680 1557829 Pmm2 phosphomannomutase 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22157680 1557829 Pmm2 phosphomannomutase 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1557829 Pmm2 phosphomannomutase 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22157680 1557829 Pmm2 phosphomannomutase 2 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16847317 1557829 Pmm2 phosphomannomutase 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22157680 1557829 Pmm2 phosphomannomutase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22157680 1557829 Pmm2 phosphomannomutase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1557829 Pmm2 phosphomannomutase 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:22157680 1557829 Pmm2 phosphomannomutase 2 gene MP:0011352 proximal convoluted tubule brush border loss IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0012325 decreased circulating antithrombin level IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1557829 Pmm2 phosphomannomutase 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1557829 Pmm2 phosphomannomutase 2 gene MP:0014045 Mallory bodies IAGP N RGD:5509061 20161229 MGI PMID:27053713 1557829 Pmm2 phosphomannomutase 2 gene MP:0030387 large posterior fontanelle IAGP N RGD:5509061 20171207 MGI PMID:27053713 1557830 Tas2r102 taste receptor, type 2, member 102 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20190502 MGI 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0000018 small ears IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0000097 short maxilla IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0000373 belly spot IEA N RGD:5509061 20111116 MGI 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23332756 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0000562 polydactyly IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:18250320 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:23332756 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:18250320 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:23332756 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0001677 absent apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:23332756 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23332756 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:23332756 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23332756 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:18250320 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:23332756 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0003142 anotia IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:23332756 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0004474 enlarged nasal bone IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0004540 small maxilla IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0004592 small mandible IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:1731393 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0004870 small premaxilla IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:23332756 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0008534 enlarged fourth ventricle IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0009048 enlarged tectum IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23332756 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0011697 lens vacuoles IEA N RGD:5509061 20141003 MGI 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0012091 increased midbrain size IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0012260 encephalomeningocele IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0012675 enlarged floor plate IAGP N RGD:5509061 20141003 MGI PMID:23332756 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0013545 cleft hard palate IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0020393 increased neuronal precursor proliferation IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0030198 nasal septum hypoplasia IAGP N RGD:5509061 20221013 MGI PMID:34887903 1557831 Gpr161 G protein-coupled receptor 161 gene MP:0031442 enlarged cerebral aqueduct IAGP N RGD:5509061 20221103 MGI PMID:34887903 1557832 Glod5 glyoxalase domain containing 5 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1557833 Zfp467 zinc finger protein 467 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0010932 increased trabecular bone connectivity density IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0010961 increased compact bone mass IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0013618 decreased areal bone mineral density IAGP N RGD:5509061 20220922 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557833 Zfp467 zinc finger protein 467 gene MP:0031008 decreased bone marrow adipose tissue amount IAGP N RGD:5509061 20210610 MGI PMID:33359894 1557834 Smarca1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:22516202 1557834 Smarca1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22516202 1557834 Smarca1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22516202 1557834 Smarca1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:22516202 1557834 Smarca1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22516202 1557834 Smarca1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:22516202 1557834 Smarca1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:22516202 1557834 Smarca1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:22516202 1557834 Smarca1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:22516202 1557834 Smarca1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:22516202 1557834 Smarca1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 gene MP:0014560 increased cortical ventricular zone cell density IAGP N RGD:5509061 20241031 MGI PMID:22516202 1557835 Stk26 serine/threonine kinase 26 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20210520 MGI 1557835 Stk26 serine/threonine kinase 26 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20200514 MGI 1557835 Stk26 serine/threonine kinase 26 gene MP:0000642 enlarged adrenal glands IEA N RGD:5509061 20200514 MGI 1557835 Stk26 serine/threonine kinase 26 gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20200514 MGI 1557835 Stk26 serine/threonine kinase 26 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20200514 MGI 1557835 Stk26 serine/threonine kinase 26 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1557835 Stk26 serine/threonine kinase 26 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20230629 MGI PMID:34240584 1557835 Stk26 serine/threonine kinase 26 gene MP:0003450 enlarged pancreas IEA N RGD:5509061 20200514 MGI 1557835 Stk26 serine/threonine kinase 26 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20210513 MGI PMID:32271880 1557835 Stk26 serine/threonine kinase 26 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20230629 MGI PMID:34240584 1557835 Stk26 serine/threonine kinase 26 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20230629 MGI PMID:34240584 1557835 Stk26 serine/threonine kinase 26 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20210826 MGI 1557835 Stk26 serine/threonine kinase 26 gene MP:0005355 enlarged thyroid gland IEA N RGD:5509061 20200514 MGI 1557835 Stk26 serine/threonine kinase 26 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1557835 Stk26 serine/threonine kinase 26 gene MP:0008039 increased NK T cell number IEA N RGD:5509061 20210520 MGI 1557835 Stk26 serine/threonine kinase 26 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20230629 MGI PMID:34240584 1557835 Stk26 serine/threonine kinase 26 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 1557835 Stk26 serine/threonine kinase 26 gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20230629 MGI PMID:34240584 1557835 Stk26 serine/threonine kinase 26 gene MP:0013958 decreased small intestine length IAGP N RGD:5509061 20230629 MGI PMID:34240584 1557836 Traf7 TNF receptor-associated factor 7 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1557836 Traf7 TNF receptor-associated factor 7 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230119 MGI 1557836 Traf7 TNF receptor-associated factor 7 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1557836 Traf7 TNF receptor-associated factor 7 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1557836 Traf7 TNF receptor-associated factor 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1557836 Traf7 TNF receptor-associated factor 7 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20230119 MGI 1557836 Traf7 TNF receptor-associated factor 7 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20230119 MGI 1557837 Mxd1 MAX dimerization protein 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:9451002 1557837 Mxd1 MAX dimerization protein 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9451002 1557837 Mxd1 MAX dimerization protein 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9451002 1557837 Mxd1 MAX dimerization protein 1 gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9451002 1557838 Foxp3 forkhead box P3 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0000019 thick ears IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0000020 scaly ears IAGP N RGD:5509061 20141003 MGI PMID:12612578 1557838 Foxp3 forkhead box P3 gene MP:0000020 scaly ears IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18725527 1557838 Foxp3 forkhead box P3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0000414 alopecia IEA N RGD:5509061 20111116 MGI 1557838 Foxp3 forkhead box P3 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:23281398 1557838 Foxp3 forkhead box P3 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:23281398 1557838 Foxp3 forkhead box P3 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20201029 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557838 Foxp3 forkhead box P3 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12612578 1557838 Foxp3 forkhead box P3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15780990 1557838 Foxp3 forkhead box P3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17220876 1557838 Foxp3 forkhead box P3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18725527 1557838 Foxp3 forkhead box P3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23135404 1557838 Foxp3 forkhead box P3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23281398 1557838 Foxp3 forkhead box P3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20161013 MGI PMID:27410049 1557838 Foxp3 forkhead box P3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20201029 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20240627 MGI PMID:38438357 1557838 Foxp3 forkhead box P3 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20200618 MGI PMID:27410049 1557838 Foxp3 forkhead box P3 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:20072126 1557838 Foxp3 forkhead box P3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12612578 1557838 Foxp3 forkhead box P3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15780990 1557838 Foxp3 forkhead box P3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17220876 1557838 Foxp3 forkhead box P3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18725527 1557838 Foxp3 forkhead box P3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23135404 1557838 Foxp3 forkhead box P3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23281398 1557838 Foxp3 forkhead box P3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20161013 MGI PMID:27410049 1557838 Foxp3 forkhead box P3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20201029 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:23135404 1557838 Foxp3 forkhead box P3 gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:16590412 1557838 Foxp3 forkhead box P3 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:12612578 1557838 Foxp3 forkhead box P3 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:16590412 1557838 Foxp3 forkhead box P3 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:17220876 1557838 Foxp3 forkhead box P3 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:15780990 1557838 Foxp3 forkhead box P3 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:20850013 1557838 Foxp3 forkhead box P3 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:16590412 1557838 Foxp3 forkhead box P3 gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:23281398 1557838 Foxp3 forkhead box P3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240627 MGI PMID:38438357 1557838 Foxp3 forkhead box P3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12612578 1557838 Foxp3 forkhead box P3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15780990 1557838 Foxp3 forkhead box P3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16590412 1557838 Foxp3 forkhead box P3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17220876 1557838 Foxp3 forkhead box P3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:16590412 1557838 Foxp3 forkhead box P3 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:23281398 1557838 Foxp3 forkhead box P3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23281398 1557838 Foxp3 forkhead box P3 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:23135404 1557838 Foxp3 forkhead box P3 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:23281398 1557838 Foxp3 forkhead box P3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0001655 multifocal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19661482 1557838 Foxp3 forkhead box P3 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17220876 1557838 Foxp3 forkhead box P3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17353370 1557838 Foxp3 forkhead box P3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18209052 1557838 Foxp3 forkhead box P3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20240627 MGI PMID:38438357 1557838 Foxp3 forkhead box P3 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18725527 1557838 Foxp3 forkhead box P3 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:23281398 1557838 Foxp3 forkhead box P3 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:17220874 1557838 Foxp3 forkhead box P3 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23135404 1557838 Foxp3 forkhead box P3 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0001849 ear inflammation IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:20850013 1557838 Foxp3 forkhead box P3 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18725525 1557838 Foxp3 forkhead box P3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18725527 1557838 Foxp3 forkhead box P3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18387831 1557838 Foxp3 forkhead box P3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18725525 1557838 Foxp3 forkhead box P3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18725527 1557838 Foxp3 forkhead box P3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20170427 MGI PMID:17207605 1557838 Foxp3 forkhead box P3 gene MP:0001863 blood vessel inflammation IAGP N RGD:5509061 20141003 MGI PMID:18725527 1557838 Foxp3 forkhead box P3 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20161013 MGI PMID:27410049 1557838 Foxp3 forkhead box P3 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20170427 MGI PMID:17207605 1557838 Foxp3 forkhead box P3 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20240627 MGI PMID:38438357 1557838 Foxp3 forkhead box P3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16590412 1557838 Foxp3 forkhead box P3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17220876 1557838 Foxp3 forkhead box P3 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16590412 1557838 Foxp3 forkhead box P3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16590412 1557838 Foxp3 forkhead box P3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17220874 1557838 Foxp3 forkhead box P3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17220876 1557838 Foxp3 forkhead box P3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18725527 1557838 Foxp3 forkhead box P3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23135404 1557838 Foxp3 forkhead box P3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0002083 premature death IAGP N RGD:5509061 20161013 MGI PMID:27410049 1557838 Foxp3 forkhead box P3 gene MP:0002083 premature death IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557838 Foxp3 forkhead box P3 gene MP:0002083 premature death IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:23135404 1557838 Foxp3 forkhead box P3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17353370 1557838 Foxp3 forkhead box P3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20072126 1557838 Foxp3 forkhead box P3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24164480 1557838 Foxp3 forkhead box P3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12612578 1557838 Foxp3 forkhead box P3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15780990 1557838 Foxp3 forkhead box P3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15795373 1557838 Foxp3 forkhead box P3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17220874 1557838 Foxp3 forkhead box P3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17220876 1557838 Foxp3 forkhead box P3 gene MP:0002221 abnormal lymph organ size IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0002281 abnormal respiratory mucosa goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002347 abnormal lymph node T cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:20072126 1557838 Foxp3 forkhead box P3 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24164480 1557838 Foxp3 forkhead box P3 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19661482 1557838 Foxp3 forkhead box P3 gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20240613 MGI PMID:38329807 1557838 Foxp3 forkhead box P3 gene MP:0002424 abnormal reticulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12612578 1557838 Foxp3 forkhead box P3 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24164480 1557838 Foxp3 forkhead box P3 gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18504307 1557838 Foxp3 forkhead box P3 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20201029 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20240613 MGI PMID:38329807 1557838 Foxp3 forkhead box P3 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0002496 increased IgD level IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20201029 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20201029 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0002534 abnormal type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18387831 1557838 Foxp3 forkhead box P3 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:19661482 1557838 Foxp3 forkhead box P3 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002670 absent scrotum IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20201029 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0002771 absent prostate gland anterior lobe IEA N RGD:5509061 20111116 MGI 1557838 Foxp3 forkhead box P3 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:18387831 1557838 Foxp3 forkhead box P3 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557838 Foxp3 forkhead box P3 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19661482 1557838 Foxp3 forkhead box P3 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0003292 melena IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20201029 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557838 Foxp3 forkhead box P3 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0003550 short perineum IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20111116 MGI 1557838 Foxp3 forkhead box P3 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:17220876 1557838 Foxp3 forkhead box P3 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:20850013 1557838 Foxp3 forkhead box P3 gene MP:0003853 dry skin IEA N RGD:5509061 20111116 MGI 1557838 Foxp3 forkhead box P3 gene MP:0003865 lymph node inflammation IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0003936 abnormal reproductive system development IEA N RGD:5509061 20111116 MGI 1557838 Foxp3 forkhead box P3 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20850013 1557838 Foxp3 forkhead box P3 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17220876 1557838 Foxp3 forkhead box P3 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20240620 MGI PMID:33355624 1557838 Foxp3 forkhead box P3 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:23281398 1557838 Foxp3 forkhead box P3 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20201029 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:17581588 1557838 Foxp3 forkhead box P3 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20150730 MGI PMID:26077720 1557838 Foxp3 forkhead box P3 gene MP:0004941 abnormal regulatory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18725527 1557838 Foxp3 forkhead box P3 gene MP:0004941 abnormal regulatory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20072126 1557838 Foxp3 forkhead box P3 gene MP:0004941 abnormal regulatory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21468021 1557838 Foxp3 forkhead box P3 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18209052 1557838 Foxp3 forkhead box P3 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18387831 1557838 Foxp3 forkhead box P3 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20493730 1557838 Foxp3 forkhead box P3 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21468021 1557838 Foxp3 forkhead box P3 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23135404 1557838 Foxp3 forkhead box P3 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557838 Foxp3 forkhead box P3 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20240620 MGI PMID:33355624 1557838 Foxp3 forkhead box P3 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:12612578 1557838 Foxp3 forkhead box P3 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:23281398 1557838 Foxp3 forkhead box P3 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20170427 MGI PMID:17207605 1557838 Foxp3 forkhead box P3 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0004972 abnormal regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:24164480 1557838 Foxp3 forkhead box P3 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:17481928 1557838 Foxp3 forkhead box P3 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:17581588 1557838 Foxp3 forkhead box P3 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:20850013 1557838 Foxp3 forkhead box P3 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21435587 1557838 Foxp3 forkhead box P3 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23135404 1557838 Foxp3 forkhead box P3 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23805138 1557838 Foxp3 forkhead box P3 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18209052 1557838 Foxp3 forkhead box P3 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:20072126 1557838 Foxp3 forkhead box P3 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21460251 1557838 Foxp3 forkhead box P3 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23281398 1557838 Foxp3 forkhead box P3 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20161013 MGI PMID:27410049 1557838 Foxp3 forkhead box P3 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20201029 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557838 Foxp3 forkhead box P3 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20240620 MGI PMID:33355624 1557838 Foxp3 forkhead box P3 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1557838 Foxp3 forkhead box P3 gene MP:0004975 absent regulatory T cells IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23281398 1557838 Foxp3 forkhead box P3 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20072126 1557838 Foxp3 forkhead box P3 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23135404 1557838 Foxp3 forkhead box P3 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20201029 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557838 Foxp3 forkhead box P3 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17353370 1557838 Foxp3 forkhead box P3 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23281398 1557838 Foxp3 forkhead box P3 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20240627 MGI PMID:38438357 1557838 Foxp3 forkhead box P3 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0005159 azoospermia IEA N RGD:5509061 20111116 MGI 1557838 Foxp3 forkhead box P3 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:20072126 1557838 Foxp3 forkhead box P3 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:17220876 1557838 Foxp3 forkhead box P3 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:20850013 1557838 Foxp3 forkhead box P3 gene MP:0005251 blepharitis IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23135404 1557838 Foxp3 forkhead box P3 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:12612578 1557838 Foxp3 forkhead box P3 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:15780990 1557838 Foxp3 forkhead box P3 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:23281398 1557838 Foxp3 forkhead box P3 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20161013 MGI PMID:27410049 1557838 Foxp3 forkhead box P3 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20240620 MGI PMID:33355624 1557838 Foxp3 forkhead box P3 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12612578 1557838 Foxp3 forkhead box P3 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17220876 1557838 Foxp3 forkhead box P3 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:21460251 1557838 Foxp3 forkhead box P3 gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557838 Foxp3 forkhead box P3 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557838 Foxp3 forkhead box P3 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557838 Foxp3 forkhead box P3 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557838 Foxp3 forkhead box P3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23135404 1557838 Foxp3 forkhead box P3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20240613 MGI PMID:38329807 1557838 Foxp3 forkhead box P3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24164480 1557838 Foxp3 forkhead box P3 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17581588 1557838 Foxp3 forkhead box P3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18725527 1557838 Foxp3 forkhead box P3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23135404 1557838 Foxp3 forkhead box P3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557838 Foxp3 forkhead box P3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20240620 MGI PMID:33355624 1557838 Foxp3 forkhead box P3 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24164480 1557838 Foxp3 forkhead box P3 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20200618 MGI PMID:27410049 1557838 Foxp3 forkhead box P3 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0008141 decreased small intestinal microvillus size IAGP N RGD:5509061 20201029 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20201029 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19661482 1557838 Foxp3 forkhead box P3 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0008397 abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12612578 1557838 Foxp3 forkhead box P3 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20201029 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20240613 MGI PMID:38329807 1557838 Foxp3 forkhead box P3 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20240620 MGI PMID:33355624 1557838 Foxp3 forkhead box P3 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0008559 abnormal interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18725527 1557838 Foxp3 forkhead box P3 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23135404 1557838 Foxp3 forkhead box P3 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20850013 1557838 Foxp3 forkhead box P3 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:17581588 1557838 Foxp3 forkhead box P3 gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0008626 increased circulating interleukin-5 level IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0008626 increased circulating interleukin-5 level IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:18387831 1557838 Foxp3 forkhead box P3 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557838 Foxp3 forkhead box P3 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:17581588 1557838 Foxp3 forkhead box P3 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0008698 abnormal interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:18725527 1557838 Foxp3 forkhead box P3 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18845758 1557838 Foxp3 forkhead box P3 gene MP:0008894 abnormal intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20072126 1557838 Foxp3 forkhead box P3 gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17136045 1557838 Foxp3 forkhead box P3 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:23135404 1557838 Foxp3 forkhead box P3 gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:12612578 1557838 Foxp3 forkhead box P3 gene MP:0010183 abnormal CD4-positive helper T cell morphology IAGP N RGD:5509061 20240627 MGI PMID:34709178 1557838 Foxp3 forkhead box P3 gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20201029 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20240613 MGI PMID:38329807 1557838 Foxp3 forkhead box P3 gene MP:0010334 pleural effusion IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0011015 decreased body surface temperature IAGP N RGD:5509061 20161124 MGI PMID:26317471 1557838 Foxp3 forkhead box P3 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:2320565 1557838 Foxp3 forkhead box P3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16275384 1557838 Foxp3 forkhead box P3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17273171 1557838 Foxp3 forkhead box P3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7930593 1557838 Foxp3 forkhead box P3 gene MP:0011224 abnormal lymph node medullary cord morphology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557838 Foxp3 forkhead box P3 gene MP:0011887 decreased circulating lipase level IAGP N RGD:5509061 20161013 MGI PMID:27410049 1557838 Foxp3 forkhead box P3 gene MP:0012078 abnormal tail ring morphology IAGP N RGD:5509061 20170309 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0012188 increased regulatory T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24135136 1557838 Foxp3 forkhead box P3 gene MP:0012188 increased regulatory T cell apoptosis IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557838 Foxp3 forkhead box P3 gene MP:0012246 abnormal hepatic cord morphology IAGP N RGD:5509061 20141003 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0012763 abnormal alpha-beta T cell number IAGP N RGD:5509061 20240613 MGI PMID:38329807 1557838 Foxp3 forkhead box P3 gene MP:0013295 pancreas atrophy IAGP N RGD:5509061 20161013 MGI PMID:27410049 1557838 Foxp3 forkhead box P3 gene MP:0013772 increased effector memory T-helper cell number IAGP N RGD:5509061 20161013 MGI PMID:27410049 1557838 Foxp3 forkhead box P3 gene MP:0014262 increased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:31296356 1557838 Foxp3 forkhead box P3 gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20240104 MGI PMID:2053595 1557838 Foxp3 forkhead box P3 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:26317471 1557838 Foxp3 forkhead box P3 gene MP:0031068 decreased blood oxygen saturation level IAGP N RGD:5509061 20200618 MGI PMID:26317471 1557838 Foxp3 forkhead box P3 gene MP:0031269 increased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20231214 MGI PMID:37277640 1557842 Trib2 tribbles pseudokinase 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1557842 Trib2 tribbles pseudokinase 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20141003 MGI 1557842 Trib2 tribbles pseudokinase 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18593568 1557842 Trib2 tribbles pseudokinase 2 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1557842 Trib2 tribbles pseudokinase 2 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1557842 Trib2 tribbles pseudokinase 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20141003 MGI 1557842 Trib2 tribbles pseudokinase 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20141003 MGI 1557842 Trib2 tribbles pseudokinase 2 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0010014 hippocampus pyramidal cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557842 Trib2 tribbles pseudokinase 2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:21900558 1557842 Trib2 tribbles pseudokinase 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1557844 Gipc3 GIPC PDZ domain containing family, member 3 gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20210826 MGI 1557844 Gipc3 GIPC PDZ domain containing family, member 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1557844 Gipc3 GIPC PDZ domain containing family, member 3 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20160421 MGI 1557844 Gipc3 GIPC PDZ domain containing family, member 3 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1557844 Gipc3 GIPC PDZ domain containing family, member 3 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210826 MGI 1557844 Gipc3 GIPC PDZ domain containing family, member 3 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20220519 MGI 1557844 Gipc3 GIPC PDZ domain containing family, member 3 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1557844 Gipc3 GIPC PDZ domain containing family, member 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1557844 Gipc3 GIPC PDZ domain containing family, member 3 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1557844 Gipc3 GIPC PDZ domain containing family, member 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1557844 Gipc3 GIPC PDZ domain containing family, member 3 gene MP:0010511 shortened PR interval IEA N RGD:5509061 20240523 MGI 1557844 Gipc3 GIPC PDZ domain containing family, member 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16426780 1557847 Klhl24 kelch-like 24 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230223 MGI PMID:27798626 1557847 Klhl24 kelch-like 24 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230223 MGI PMID:27798626 1557847 Klhl24 kelch-like 24 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230223 MGI PMID:27798626 1557847 Klhl24 kelch-like 24 gene MP:0005114 premature hair loss IAGP N RGD:5509061 20230223 MGI PMID:27798626 1557847 Klhl24 kelch-like 24 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20230223 MGI PMID:27798626 1557850 Irx2 Iroquois homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14585979 1557851 Acrbp proacrosin binding protein gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:11994540 1557851 Acrbp proacrosin binding protein gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220421 MGI PMID:30606959 1557851 Acrbp proacrosin binding protein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0001925 male infertility IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20220421 MGI PMID:30606959 1557851 Acrbp proacrosin binding protein gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220421 MGI PMID:30606959 1557851 Acrbp proacrosin binding protein gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20220421 MGI PMID:30606959 1557851 Acrbp proacrosin binding protein gene MP:0005411 delayed fertilization IAGP N RGD:5509061 20141003 MGI PMID:11994540 1557851 Acrbp proacrosin binding protein gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220421 MGI PMID:30606959 1557851 Acrbp proacrosin binding protein gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0030977 impaired sperm-egg recognition IAGP N RGD:5509061 20220421 MGI PMID:30606959 1557851 Acrbp proacrosin binding protein gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0031009 abnormal sperm-egg fusion IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557851 Acrbp proacrosin binding protein gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220421 MGI PMID:30606959 1557851 Acrbp proacrosin binding protein gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220303 MGI PMID:27303034 1557852 Msr1 macrophage scavenger receptor 1 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16339556 1557852 Msr1 macrophage scavenger receptor 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16339556 1557852 Msr1 macrophage scavenger receptor 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15145948 1557852 Msr1 macrophage scavenger receptor 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16339556 1557852 Msr1 macrophage scavenger receptor 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16339556 1557852 Msr1 macrophage scavenger receptor 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:10550330 1557852 Msr1 macrophage scavenger receptor 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:10550330 1557852 Msr1 macrophage scavenger receptor 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9069289 1557852 Msr1 macrophage scavenger receptor 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:9069289 1557852 Msr1 macrophage scavenger receptor 1 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20180125 MGI PMID:28970238 1557852 Msr1 macrophage scavenger receptor 1 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:11412310 1557852 Msr1 macrophage scavenger receptor 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9069289 1557852 Msr1 macrophage scavenger receptor 1 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:9069289 1557856 Usp26 ubiquitin specific peptidase 26 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20210923 MGI PMID:30561524 1557856 Usp26 ubiquitin specific peptidase 26 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20210923 MGI PMID:30561524 1557856 Usp26 ubiquitin specific peptidase 26 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20210923 MGI PMID:30561524 1557856 Usp26 ubiquitin specific peptidase 26 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210923 MGI PMID:30561524 1557856 Usp26 ubiquitin specific peptidase 26 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20210923 MGI PMID:30561524 1557856 Usp26 ubiquitin specific peptidase 26 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210923 MGI PMID:30561524 1557856 Usp26 ubiquitin specific peptidase 26 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20210923 MGI PMID:30561524 1557856 Usp26 ubiquitin specific peptidase 26 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20210923 MGI PMID:30561524 1557856 Usp26 ubiquitin specific peptidase 26 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20210923 MGI PMID:30561524 1557857 Klf8 Kruppel-like transcription factor 8 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23716600 1557857 Klf8 Kruppel-like transcription factor 8 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20111116 MGI 1557857 Klf8 Kruppel-like transcription factor 8 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23716600 1557857 Klf8 Kruppel-like transcription factor 8 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23716600 1557857 Klf8 Kruppel-like transcription factor 8 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23716600 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0000828 abnormal fourth ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:23431188 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:23431188 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23431188 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:23431188 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:23431188 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0009703 decreased birth body size IEA N RGD:5509061 20111116 MGI 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0011087 neonatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23431188 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:23824717 1557858 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20240215 MGI PMID:35436587 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20240215 MGI PMID:35436587 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20240215 MGI PMID:35436587 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20240215 MGI PMID:35436587 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0005331 insulin resistance IAGP N RGD:5509061 20240215 MGI PMID:35436587 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20240215 MGI PMID:35436587 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20240215 MGI PMID:35436587 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20240215 MGI PMID:35436587 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20240215 MGI PMID:35436587 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20240215 MGI PMID:35436587 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20240215 MGI PMID:35436587 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20240215 MGI PMID:35436587 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20240215 MGI PMID:35436587 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20240215 MGI PMID:35436587 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0031600 increased white adipose tissue apoptosis IAGP N RGD:5509061 20240229 MGI PMID:35436587 1557859 Serpina3c serine (or cysteine) peptidase inhibitor, clade A, member 3C gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240418 MGI PMID:35436587 1557860 Polr3b polymerase (RNA) III (DNA directed) polypeptide B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20190502 MGI 1557860 Polr3b polymerase (RNA) III (DNA directed) polypeptide B gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1557860 Polr3b polymerase (RNA) III (DNA directed) polypeptide B gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0002223 lymphoid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557861 Sash3 SAM and SH3 domain containing 3 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:16227612 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:15256482 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:19887680 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15314648 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:19887680 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:12925582 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19887680 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0000927 small floor plate IAGP N RGD:5509061 20141003 MGI PMID:19887680 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19887680 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:19887680 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:12925582 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12925582 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0002958 cerebral aqueductal stenosis IAGP N RGD:5509061 20141003 MGI PMID:12925582 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12925582 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0009717 absent subcommissural organ IAGP N RGD:5509061 20141003 MGI PMID:12925582 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:19887680 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0011058 abnormal spinal cord motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:19887680 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19887680 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12925582 1557863 Rfx4 regulatory factor X, 4 (influences HLA class II expression) gene MP:0014402 abnormal Reissner's fiber morphology IAGP N RGD:5509061 20240321 MGI PMID:12925582 1557864 Helq helicase, POLQ-like gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1557864 Helq helicase, POLQ-like gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1557864 Helq helicase, POLQ-like gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210520 MGI 1557864 Helq helicase, POLQ-like gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1557864 Helq helicase, POLQ-like gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1557864 Helq helicase, POLQ-like gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1557864 Helq helicase, POLQ-like gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1557864 Helq helicase, POLQ-like gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20220811 MGI 1557864 Helq helicase, POLQ-like gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1557864 Helq helicase, POLQ-like gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20231207 MGI 1557864 Helq helicase, POLQ-like gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20231207 MGI 1557864 Helq helicase, POLQ-like gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 1557864 Helq helicase, POLQ-like gene MP:0010288 increased gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557864 Helq helicase, POLQ-like gene MP:0012437 increased Harderian gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24005329 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20180222 MGI PMID:27892606 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0001785 edema IAGP N RGD:5509061 20180222 MGI PMID:27892606 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0001874 acanthosis IAGP N RGD:5509061 20180222 MGI PMID:27892606 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20190404 MGI PMID:28179432 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20180222 MGI PMID:27892606 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20180222 MGI PMID:27892606 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20230824 MGI PMID:33762433 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20210128 MGI 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0003390 lymphedema IAGP N RGD:5509061 20190404 MGI PMID:28179432 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20220519 MGI 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20190404 MGI PMID:28179432 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0009931 abnormal skin appearance IEA N RGD:5509061 20160811 MGI 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20220519 MGI 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20180222 MGI PMID:27892606 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0011239 abnormal skin coloration IAGP N RGD:5509061 20180222 MGI PMID:27892606 1557866 Svep1 sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1 gene MP:0012269 nuchal edema IAGP N RGD:5509061 20190404 MGI PMID:28179432 1557867 Arhgap28 Rho GTPase activating protein 28 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1557867 Arhgap28 Rho GTPase activating protein 28 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1557867 Arhgap28 Rho GTPase activating protein 28 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20210128 MGI 1557867 Arhgap28 Rho GTPase activating protein 28 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230601 MGI 1557867 Arhgap28 Rho GTPase activating protein 28 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1557867 Arhgap28 Rho GTPase activating protein 28 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160317 MGI PMID:25211221 1557867 Arhgap28 Rho GTPase activating protein 28 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210826 MGI 1557867 Arhgap28 Rho GTPase activating protein 28 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20210826 MGI 1557867 Arhgap28 Rho GTPase activating protein 28 gene MP:0009084 blind uterus IEA N RGD:5509061 20210520 MGI 1557867 Arhgap28 Rho GTPase activating protein 28 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17431507 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:17431507 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17717301 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21098440 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22828895 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:16407108 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17431507 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:23152493 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141218 MGI PMID:24441828 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:23666671 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:15890976 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:18419777 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:19603549 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:23152493 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20190228 MGI PMID:27482086 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20210422 MGI PMID:33536282 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:22869620 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16785989 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16785989 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22869620 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002083 premature death IAGP N RGD:5509061 20141225 MGI PMID:24743769 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9628868 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:9628868 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:9628868 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002220 large lymphoid organs IAGP N RGD:5509061 20160421 MGI PMID:25087098 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20190228 MGI PMID:27482086 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20160421 MGI PMID:25087098 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17431507 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:22869620 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:23666671 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:18483626 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20190228 MGI PMID:27482086 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:23666671 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141218 MGI PMID:24441828 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0003057 abnormal epicardium morphology IAGP N RGD:5509061 20141003 MGI PMID:9628868 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17431507 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:22869620 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20190228 MGI PMID:27482086 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23666671 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21098440 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23666671 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9628868 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:18483626 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:21098440 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:22828895 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:23363625 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004122 abnormal sinus arrhythmia IAGP N RGD:5509061 20141003 MGI PMID:22869620 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18483626 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:16873551 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:18419777 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:18483626 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:19603549 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:20224043 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:21768539 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:23152493 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141218 MGI PMID:24441828 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141225 MGI PMID:24743769 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20180111 MGI PMID:25775566 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20210422 MGI PMID:33536282 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:19603549 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:18483626 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:21098440 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20210422 MGI PMID:33536282 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:16785989 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20190228 MGI PMID:27482086 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20160421 MGI PMID:25087098 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20160421 MGI PMID:25087098 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:18483626 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20190228 MGI PMID:27482086 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16873551 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21098440 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:22869620 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20160421 MGI PMID:25087098 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:16873551 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:22869620 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17431507 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:21098440 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:22869620 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141225 MGI PMID:24743769 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20180111 MGI PMID:25775566 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20190228 MGI PMID:27482086 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20210422 MGI PMID:33536282 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20210422 MGI PMID:33536282 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17431507 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0006110 ventricular fibrillation IAGP N RGD:5509061 20141003 MGI PMID:15890976 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0006110 ventricular fibrillation IAGP N RGD:5509061 20180111 MGI PMID:25775566 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0006110 ventricular fibrillation IAGP N RGD:5509061 20190228 MGI PMID:27482086 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:22869620 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20160421 MGI PMID:25087098 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0008543 atrial fibrillation IAGP N RGD:5509061 20141003 MGI PMID:22828895 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18483626 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9628868 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20224043 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21743453 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:15890976 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:16873551 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:18419777 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:18483626 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:20224043 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:21098440 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:21743453 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:21768539 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0009559 thymus cortex hyperplasia IAGP N RGD:5509061 20160421 MGI PMID:25087098 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20141003 MGI PMID:16873551 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20141003 MGI PMID:21098440 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20141003 MGI PMID:23152493 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18483626 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21098440 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20190228 MGI PMID:27482086 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0010505 abnormal T wave IAGP N RGD:5509061 20141003 MGI PMID:22869620 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20190228 MGI PMID:27482086 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:22869620 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20190228 MGI PMID:27482086 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20141003 MGI PMID:22869620 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:23666671 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:17431507 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17431507 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20180111 MGI PMID:25775566 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210422 MGI PMID:33536282 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23152493 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141225 MGI PMID:24743769 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9628868 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141218 MGI PMID:24441828 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18483626 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20240404 MGI PMID:9628868 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20210422 MGI PMID:33536282 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0014253 decreased paired-pulse ratio IAGP N RGD:5509061 20230706 MGI PMID:27482086 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0020346 abnormal myocardial fiber calcium currents IAGP N RGD:5509061 20210422 MGI PMID:33536282 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0020347 abnormal myocardial fiber sodium currents IAGP N RGD:5509061 20210422 MGI PMID:33536282 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0031607 abnormal fetal cardiomyocyte mitochondrial morphology IAGP N RGD:5509061 20240404 MGI PMID:9628868 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0031614 fetal cardiomyocyte vacuoles IAGP N RGD:5509061 20240404 MGI PMID:9628868 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:17431507 1557868 Ryr2 ryanodine receptor 2, cardiac gene MP:0031634 decreased heart right ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:16873551 1557870 Rps6ka6 ribosomal protein S6 kinase polypeptide 6 gene MP:0000267 abnormal heart development IEA N RGD:5509061 20111116 MGI 1557870 Rps6ka6 ribosomal protein S6 kinase polypeptide 6 gene MP:0000433 microcephaly IEA N RGD:5509061 20111116 MGI 1557870 Rps6ka6 ribosomal protein S6 kinase polypeptide 6 gene MP:0001695 abnormal gastrulation IEA N RGD:5509061 20111116 MGI 1557870 Rps6ka6 ribosomal protein S6 kinase polypeptide 6 gene MP:0002230 abnormal primitive streak formation IEA N RGD:5509061 20111116 MGI 1557870 Rps6ka6 ribosomal protein S6 kinase polypeptide 6 gene MP:0002231 abnormal primitive streak morphology IEA N RGD:5509061 20111116 MGI 1557870 Rps6ka6 ribosomal protein S6 kinase polypeptide 6 gene MP:0004073 caudal body truncation IEA N RGD:5509061 20240118 MGI 1557870 Rps6ka6 ribosomal protein S6 kinase polypeptide 6 gene MP:0004180 failure of initiation of embryo turning IEA N RGD:5509061 20111116 MGI 1557870 Rps6ka6 ribosomal protein S6 kinase polypeptide 6 gene MP:0009331 absent primitive node IEA N RGD:5509061 20111116 MGI 1557870 Rps6ka6 ribosomal protein S6 kinase polypeptide 6 gene MP:0009657 failure of chorioallantoic fusion IEA N RGD:5509061 20111116 MGI 1557870 Rps6ka6 ribosomal protein S6 kinase polypeptide 6 gene MP:0012082 delayed heart development IEA N RGD:5509061 20240118 MGI 1557871 Ly75 lymphocyte antigen 75 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10784619 1557871 Ly75 lymphocyte antigen 75 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15024047 1557871 Ly75 lymphocyte antigen 75 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22736794 1557874 Prpf38b PRP38 pre-mRNA processing factor 38 (yeast) domain containing B gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1557874 Prpf38b PRP38 pre-mRNA processing factor 38 (yeast) domain containing B gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1557874 Prpf38b PRP38 pre-mRNA processing factor 38 (yeast) domain containing B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557875 Zfp398 zinc finger protein 398 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1557875 Zfp398 zinc finger protein 398 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1557875 Zfp398 zinc finger protein 398 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210128 MGI 1557875 Zfp398 zinc finger protein 398 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1557875 Zfp398 zinc finger protein 398 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220811 MGI 1557875 Zfp398 zinc finger protein 398 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 1557875 Zfp398 zinc finger protein 398 gene MP:0009477 small cecum IEA N RGD:5509061 20210128 MGI 1557876 Rad51c RAD51 paralog C gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20471405 1557876 Rad51c RAD51 paralog C gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20471405 1557876 Rad51c RAD51 paralog C gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17312021 1557876 Rad51c RAD51 paralog C gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20471405 1557878 Wdr53 WD repeat domain 53 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1557878 Wdr53 WD repeat domain 53 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20220811 MGI 1557878 Wdr53 WD repeat domain 53 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1557878 Wdr53 WD repeat domain 53 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1557878 Wdr53 WD repeat domain 53 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1557878 Wdr53 WD repeat domain 53 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230601 MGI 1557878 Wdr53 WD repeat domain 53 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20230601 MGI 1557879 Sh2d1a SH2 domain containing 1A gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11404475 1557879 Sh2d1a SH2 domain containing 1A gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:12966553 1557879 Sh2d1a SH2 domain containing 1A gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:16365433 1557879 Sh2d1a SH2 domain containing 1A gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:15774582 1557879 Sh2d1a SH2 domain containing 1A gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:22613797 1557879 Sh2d1a SH2 domain containing 1A gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12966553 1557879 Sh2d1a SH2 domain containing 1A gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15774582 1557879 Sh2d1a SH2 domain containing 1A gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:20153220 1557879 Sh2d1a SH2 domain containing 1A gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22613797 1557879 Sh2d1a SH2 domain containing 1A gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15774582 1557879 Sh2d1a SH2 domain containing 1A gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:18212118 1557879 Sh2d1a SH2 domain containing 1A gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22613797 1557879 Sh2d1a SH2 domain containing 1A gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:11404475 1557879 Sh2d1a SH2 domain containing 1A gene MP:0002433 abnormal T-helper 1 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11404475 1557879 Sh2d1a SH2 domain containing 1A gene MP:0002434 abnormal T-helper 2 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11404475 1557879 Sh2d1a SH2 domain containing 1A gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12966553 1557879 Sh2d1a SH2 domain containing 1A gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:22613797 1557879 Sh2d1a SH2 domain containing 1A gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11323694 1557879 Sh2d1a SH2 domain containing 1A gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11404475 1557879 Sh2d1a SH2 domain containing 1A gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12966553 1557879 Sh2d1a SH2 domain containing 1A gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:15539156 1557879 Sh2d1a SH2 domain containing 1A gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:18212118 1557879 Sh2d1a SH2 domain containing 1A gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:12966553 1557879 Sh2d1a SH2 domain containing 1A gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11323694 1557879 Sh2d1a SH2 domain containing 1A gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15123745 1557879 Sh2d1a SH2 domain containing 1A gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:16365433 1557879 Sh2d1a SH2 domain containing 1A gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15774582 1557879 Sh2d1a SH2 domain containing 1A gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:11323694 1557879 Sh2d1a SH2 domain containing 1A gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15123745 1557879 Sh2d1a SH2 domain containing 1A gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:11404475 1557879 Sh2d1a SH2 domain containing 1A gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:16127454 1557879 Sh2d1a SH2 domain containing 1A gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:20962259 1557879 Sh2d1a SH2 domain containing 1A gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22683123 1557879 Sh2d1a SH2 domain containing 1A gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:22683123 1557879 Sh2d1a SH2 domain containing 1A gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11323694 1557879 Sh2d1a SH2 domain containing 1A gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11404475 1557879 Sh2d1a SH2 domain containing 1A gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15539156 1557879 Sh2d1a SH2 domain containing 1A gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20153220 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008036 abnormal NK T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23430111 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:15749842 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:18212118 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:22613797 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008041 absent NK T cells IAGP N RGD:5509061 20141003 MGI PMID:15749842 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22613797 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23430111 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15539156 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20153220 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12966553 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008176 abnormal germinal center B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22613797 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:18212118 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:22613797 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:15749842 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22613797 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:15774582 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15774582 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18212118 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:18212118 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:18212118 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:18212118 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:15774582 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22683123 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22683124 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23430111 1557879 Sh2d1a SH2 domain containing 1A gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:23430111 1557879 Sh2d1a SH2 domain containing 1A gene MP:0009058 decreased interleukin-21 secretion IAGP N RGD:5509061 20141003 MGI PMID:20153220 1557879 Sh2d1a SH2 domain containing 1A gene MP:0010084 abnormal long lived plasma cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20153220 1557879 Sh2d1a SH2 domain containing 1A gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22683124 1557879 Sh2d1a SH2 domain containing 1A gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:11323694 1557879 Sh2d1a SH2 domain containing 1A gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:11404475 1557880 Dmrtb1 DMRT-like family B with proline-rich C-terminal, 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20160225 MGI PMID:25249458 1557880 Dmrtb1 DMRT-like family B with proline-rich C-terminal, 1 gene MP:0001147 small testis IAGP N RGD:5509061 20160225 MGI PMID:25249458 1557880 Dmrtb1 DMRT-like family B with proline-rich C-terminal, 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20160225 MGI PMID:25249458 1557880 Dmrtb1 DMRT-like family B with proline-rich C-terminal, 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20160225 MGI PMID:25249458 1557880 Dmrtb1 DMRT-like family B with proline-rich C-terminal, 1 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20160225 MGI PMID:25249458 1557880 Dmrtb1 DMRT-like family B with proline-rich C-terminal, 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20160225 MGI PMID:25249458 1557880 Dmrtb1 DMRT-like family B with proline-rich C-terminal, 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20160225 MGI PMID:25249458 1557880 Dmrtb1 DMRT-like family B with proline-rich C-terminal, 1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20160225 MGI PMID:25249458 1557880 Dmrtb1 DMRT-like family B with proline-rich C-terminal, 1 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20160225 MGI PMID:25249458 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20221013 MGI PMID:33771871 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20221013 MGI PMID:33771871 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20221013 MGI PMID:33771871 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20221013 MGI PMID:33771871 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20221013 MGI PMID:33771871 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20181227 MGI 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20210128 MGI 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20201231 MGI 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20210128 MGI 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20221013 MGI PMID:33771871 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20221013 MGI PMID:33771871 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20221013 MGI PMID:33771871 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20221013 MGI PMID:33771871 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20221013 MGI PMID:33771871 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0020512 abnormal dendritic mushroom spine morphology IAGP N RGD:5509061 20221013 MGI PMID:33771871 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0020514 abnormal dendritic thin spine morphology IAGP N RGD:5509061 20221013 MGI PMID:33771871 1557881 Ftsj1 FtsJ RNA 2'-O-methyltransferase 1 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20221013 MGI PMID:33771871 1557883 Stxbp3 syntaxin binding protein 3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15690082 1557883 Stxbp3 syntaxin binding protein 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15734838 1557883 Stxbp3 syntaxin binding protein 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15690082 1557883 Stxbp3 syntaxin binding protein 3 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15734838 1557883 Stxbp3 syntaxin binding protein 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15734838 1557883 Stxbp3 syntaxin binding protein 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15734838 1557883 Stxbp3 syntaxin binding protein 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15690082 1557883 Stxbp3 syntaxin binding protein 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15690082 1557883 Stxbp3 syntaxin binding protein 3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15734838 1557883 Stxbp3 syntaxin binding protein 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15690082 1557886 Nup62 nucleoporin 62 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1557886 Nup62 nucleoporin 62 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1557886 Nup62 nucleoporin 62 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20190502 MGI 1557886 Nup62 nucleoporin 62 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20141003 MGI 1557886 Nup62 nucleoporin 62 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557886 Nup62 nucleoporin 62 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1557887 Zfp512 zinc finger protein 512 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1557887 Zfp512 zinc finger protein 512 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1557887 Zfp512 zinc finger protein 512 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1557887 Zfp512 zinc finger protein 512 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201022 MGI 1557887 Zfp512 zinc finger protein 512 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 1557887 Zfp512 zinc finger protein 512 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1557888 Ulk3 unc-51-like kinase 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 1557888 Ulk3 unc-51-like kinase 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1557888 Ulk3 unc-51-like kinase 3 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1557888 Ulk3 unc-51-like kinase 3 gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1557888 Ulk3 unc-51-like kinase 3 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1557888 Ulk3 unc-51-like kinase 3 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1557888 Ulk3 unc-51-like kinase 3 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210826 MGI 1557888 Ulk3 unc-51-like kinase 3 gene MP:0004958 enlarged prostate gland IEA N RGD:5509061 20210826 MGI 1557888 Ulk3 unc-51-like kinase 3 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220519 MGI 1557888 Ulk3 unc-51-like kinase 3 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20181227 MGI 1557888 Ulk3 unc-51-like kinase 3 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220519 MGI 1557888 Ulk3 unc-51-like kinase 3 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210826 MGI 1557888 Ulk3 unc-51-like kinase 3 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210826 MGI 1557889 Gspt2 G1 to S phase transition 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1557889 Gspt2 G1 to S phase transition 2 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20201022 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11330864 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11330864 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11330864 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20230601 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0000160 kyphosis IEA N RGD:5509061 20230601 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:11330864 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11330864 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11330864 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0001260 increased body weight IEA N RGD:5509061 20111116 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20111116 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20111116 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:12431380 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11330864 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12431380 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10748463 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10748464 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10748465 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11330864 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:12431380 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0003036 vertebral transformation IEA N RGD:5509061 20230601 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0003063 increased coping response IEA N RGD:5509061 20111116 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:11330864 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:11330864 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20230601 MGI 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:18241853 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11330864 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:12431380 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11330864 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12431380 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1557890 Cer1 cerberus 1, DAN family BMP antagonist gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:12431380 1557892 Hoxa13 homeobox A13 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18483557 1557892 Hoxa13 homeobox A13 gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:12783783 1557892 Hoxa13 homeobox A13 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:5519671 1557892 Hoxa13 homeobox A13 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:5519671 1557892 Hoxa13 homeobox A13 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:17222543 1557892 Hoxa13 homeobox A13 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:22465667 1557892 Hoxa13 homeobox A13 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:11543619 1557892 Hoxa13 homeobox A13 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:11684655 1557892 Hoxa13 homeobox A13 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:15385446 1557892 Hoxa13 homeobox A13 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:15385446 1557892 Hoxa13 homeobox A13 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:11543619 1557892 Hoxa13 homeobox A13 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:11684655 1557892 Hoxa13 homeobox A13 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0000661 small prostate gland ventral lobe IAGP N RGD:5509061 20141003 MGI PMID:10210434 1557892 Hoxa13 homeobox A13 gene MP:0000666 decreased prostate gland duct number IAGP N RGD:5509061 20141003 MGI PMID:10210434 1557892 Hoxa13 homeobox A13 gene MP:0001135 abnormal uterine cervix morphology IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:10210434 1557892 Hoxa13 homeobox A13 gene MP:0001163 abnormal prostate gland anterior lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:10210434 1557892 Hoxa13 homeobox A13 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:11684655 1557892 Hoxa13 homeobox A13 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1557892 Hoxa13 homeobox A13 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18483557 1557892 Hoxa13 homeobox A13 gene MP:0001732 postnatal growth retardation IEA N RGD:5509061 20111116 MGI 1557892 Hoxa13 homeobox A13 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:18483557 1557892 Hoxa13 homeobox A13 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:5519671 1557892 Hoxa13 homeobox A13 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0002059 abnormal seminal vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10210434 1557892 Hoxa13 homeobox A13 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:11684655 1557892 Hoxa13 homeobox A13 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:5519671 1557892 Hoxa13 homeobox A13 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:5519671 1557892 Hoxa13 homeobox A13 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:11543619 1557892 Hoxa13 homeobox A13 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:15385446 1557892 Hoxa13 homeobox A13 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:5519671 1557892 Hoxa13 homeobox A13 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0002772 brachypodia IAGP N RGD:5509061 20141003 MGI PMID:11543619 1557892 Hoxa13 homeobox A13 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:5519671 1557892 Hoxa13 homeobox A13 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:5519671 1557892 Hoxa13 homeobox A13 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0003124 hypospadia IAGP N RGD:5509061 20141003 MGI PMID:12783783 1557892 Hoxa13 homeobox A13 gene MP:0003230 abnormal umbilical artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11684655 1557892 Hoxa13 homeobox A13 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0003550 short perineum IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0003617 urinary bladder hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0003800 monodactyly IAGP N RGD:5509061 20141003 MGI PMID:5519671 1557892 Hoxa13 homeobox A13 gene MP:0003800 monodactyly IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0003942 abnormal urinary system development IAGP N RGD:5509061 20141003 MGI PMID:12783783 1557892 Hoxa13 homeobox A13 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0004576 abnormal embryonic autopod plate morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0004641 elongated metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:5519671 1557892 Hoxa13 homeobox A13 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0005230 ectrodactyly IAGP N RGD:5509061 20141003 MGI PMID:11543619 1557892 Hoxa13 homeobox A13 gene MP:0005230 ectrodactyly IAGP N RGD:5509061 20141003 MGI PMID:5519671 1557892 Hoxa13 homeobox A13 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:17222543 1557892 Hoxa13 homeobox A13 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0006230 iris stroma hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11543619 1557892 Hoxa13 homeobox A13 gene MP:0006253 clinodactyly IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:11543619 1557892 Hoxa13 homeobox A13 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18483557 1557892 Hoxa13 homeobox A13 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0008919 fused tarsal bones IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0008983 small vagina IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0009001 absent hallux IAGP N RGD:5509061 20141003 MGI PMID:17222543 1557892 Hoxa13 homeobox A13 gene MP:0009049 abnormal hallux morphology IAGP N RGD:5509061 20141003 MGI PMID:17222543 1557892 Hoxa13 homeobox A13 gene MP:0009087 dilated uterine horn IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0009103 abnormal penile bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0009104 small penile bone IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0009227 uterine cervix hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0009252 absent urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0009740 small prostate gland dorsolateral lobe IAGP N RGD:5509061 20220303 MGI PMID:10210434 1557892 Hoxa13 homeobox A13 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11684655 1557892 Hoxa13 homeobox A13 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15385446 1557892 Hoxa13 homeobox A13 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11684655 1557892 Hoxa13 homeobox A13 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8898214 1557892 Hoxa13 homeobox A13 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11684655 1557892 Hoxa13 homeobox A13 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:5519671 1557892 Hoxa13 homeobox A13 gene MP:0011780 abnormal female urethra morphology IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0011828 urinary bladder cyst IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0011829 vesicovaginal fistula IAGP N RGD:5509061 20141003 MGI PMID:10569982 1557892 Hoxa13 homeobox A13 gene MP:0012302 umbilical artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:11684655 1557892 Hoxa13 homeobox A13 gene MP:0012302 umbilical artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:18483557 1557892 Hoxa13 homeobox A13 gene MP:0013318 abnormal branching involved in seminal vesicle morphogenesis IAGP N RGD:5509061 20141204 MGI PMID:10210434 1557892 Hoxa13 homeobox A13 gene MP:0013323 abnormal ampullary gland morphology IAGP N RGD:5509061 20141204 MGI PMID:10210434 1557892 Hoxa13 homeobox A13 gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:5519671 1557892 Hoxa13 homeobox A13 gene MP:0014291 decreased autopod size IAGP N RGD:5509061 20230824 MGI PMID:8898214 1557893 Bcl7b B cell CLL/lymphoma 7B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191017 MGI PMID:29213114 1557893 Bcl7b B cell CLL/lymphoma 7B gene MP:0001405 impaired coordination IAGP N RGD:5509061 20191017 MGI PMID:29213114 1557893 Bcl7b B cell CLL/lymphoma 7B gene MP:0001522 impaired swimming IAGP N RGD:5509061 20191017 MGI PMID:29213114 1557893 Bcl7b B cell CLL/lymphoma 7B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20191017 MGI PMID:29213114 1557893 Bcl7b B cell CLL/lymphoma 7B gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1557893 Bcl7b B cell CLL/lymphoma 7B gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20191017 MGI PMID:29213114 1557893 Bcl7b B cell CLL/lymphoma 7B gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1557893 Bcl7b B cell CLL/lymphoma 7B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1557893 Bcl7b B cell CLL/lymphoma 7B gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1557894 Idnk idnK gluconokinase homolog (E. coli) gene MP:0009456 impaired cued conditioning behavior IEA N RGD:5509061 20141003 MGI 1557894 Idnk idnK gluconokinase homolog (E. coli) gene MP:0020220 decreased tear production IEA N RGD:5509061 20141211 MGI 1557895 Zfp202 zinc finger protein 202 gene MP:0001258 decreased body length IEA N RGD:5509061 20160804 MGI 1557895 Zfp202 zinc finger protein 202 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1557895 Zfp202 zinc finger protein 202 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160804 MGI 1557895 Zfp202 zinc finger protein 202 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 1557895 Zfp202 zinc finger protein 202 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1557895 Zfp202 zinc finger protein 202 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1557895 Zfp202 zinc finger protein 202 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1557895 Zfp202 zinc finger protein 202 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1557897 Ntm neurotrimin gene MP:0005385 cardiovascular system phenotype IAGP N RGD:5509061 20201112 MGI PMID:24616287 1557897 Ntm neurotrimin gene MP:0012293 impaired active avoidance behavior IAGP N RGD:5509061 20190228 MGI PMID:27693610 1557897 Ntm neurotrimin gene MP:0030586 impaired behavioral response to amphetamine IAGP N RGD:5509061 20190228 MGI PMID:27693610 1557898 Peli2 pellino 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200409 MGI PMID:29674674 1557898 Peli2 pellino 2 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20200409 MGI PMID:29674674 1557898 Peli2 pellino 2 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200409 MGI PMID:29674674 1557898 Peli2 pellino 2 gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20200409 MGI PMID:29674674 1557898 Peli2 pellino 2 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200409 MGI PMID:29674674 1557898 Peli2 pellino 2 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20200409 MGI PMID:29674674 1557898 Peli2 pellino 2 gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20200409 MGI PMID:29674674 1557900 Cd209b CD209b antigen gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:15583012 1557900 Cd209b CD209b antigen gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20200618 MGI PMID:31998663 1557900 Cd209b CD209b antigen gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15583012 1557900 Cd209b CD209b antigen gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200618 MGI PMID:31998663 1557900 Cd209b CD209b antigen gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15583012 1557900 Cd209b CD209b antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557900 Cd209b CD209b antigen gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20200618 MGI PMID:31998663 1557900 Cd209b CD209b antigen gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557900 Cd209b CD209b antigen gene MP:0005635 decreased circulating bilirubin level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557900 Cd209b CD209b antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557900 Cd209b CD209b antigen gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557900 Cd209b CD209b antigen gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557900 Cd209b CD209b antigen gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20200618 MGI PMID:20130211 1557900 Cd209b CD209b antigen gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200618 MGI PMID:20130211 1557900 Cd209b CD209b antigen gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20200618 MGI PMID:20130211 1557900 Cd209b CD209b antigen gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20200618 MGI PMID:20130211 1557900 Cd209b CD209b antigen gene MP:0009646 urinary bladder inflammation IAGP N RGD:5509061 20200618 MGI PMID:31998663 1557900 Cd209b CD209b antigen gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200618 MGI PMID:15583012 1557900 Cd209b CD209b antigen gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20150226 MGI PMID:23118208 1557901 Pdp2 pyruvate dehydrogenase phosphatase catalytic subunit 2 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1557902 Cul4b cullin 4B gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22453236 1557902 Cul4b cullin 4B gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:22763239 1557902 Cul4b cullin 4B gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:22453236 1557902 Cul4b cullin 4B gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:22453236 1557902 Cul4b cullin 4B gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:22453236 1557902 Cul4b cullin 4B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22453236 1557902 Cul4b cullin 4B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0001717 absent ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:22453236 1557902 Cul4b cullin 4B gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:22453236 1557902 Cul4b cullin 4B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0002084 abnormal developmental patterning IEA N RGD:5509061 20111116 MGI 1557902 Cul4b cullin 4B gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22453236 1557902 Cul4b cullin 4B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:22763239 1557902 Cul4b cullin 4B gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22453236 1557902 Cul4b cullin 4B gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0004266 pale placenta IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22763239 1557902 Cul4b cullin 4B gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22763239 1557902 Cul4b cullin 4B gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:22763239 1557902 Cul4b cullin 4B gene MP:0010382 abnormal dosage compensation, by inactivation of X chromosome IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22453236 1557902 Cul4b cullin 4B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22453236 1557902 Cul4b cullin 4B gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0011527 disorganized placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:22453236 1557902 Cul4b cullin 4B gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:22606329 1557902 Cul4b cullin 4B gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:22763239 1557904 Hook2 hook microtubule tethering protein 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1557904 Hook2 hook microtubule tethering protein 2 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20210520 MGI 1557904 Hook2 hook microtubule tethering protein 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1557904 Hook2 hook microtubule tethering protein 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1557904 Hook2 hook microtubule tethering protein 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1557904 Hook2 hook microtubule tethering protein 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 1557904 Hook2 hook microtubule tethering protein 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20220519 MGI 1557904 Hook2 hook microtubule tethering protein 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0001147 small testis IAGP N RGD:5509061 20220623 MGI PMID:26162102 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0001147 small testis IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20160204 MGI PMID:26248850 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20160204 MGI PMID:26248850 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0001265 decreased body size IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0001925 male infertility IAGP N RGD:5509061 20160204 MGI PMID:26248850 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0001925 male infertility IAGP N RGD:5509061 20220623 MGI PMID:26162102 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0001925 male infertility IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20160204 MGI PMID:26248850 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0002083 premature death IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220623 MGI PMID:26162102 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0005159 azoospermia IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20160204 MGI PMID:26248850 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20220623 MGI PMID:26162102 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220623 MGI PMID:26162102 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0009231 detached acrosome IAGP N RGD:5509061 20220623 MGI PMID:26162102 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20220623 MGI PMID:26162102 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220623 MGI PMID:26162102 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20220623 MGI PMID:26162102 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0013598 Leydig cell hypertrophy IAGP N RGD:5509061 20160204 MGI PMID:26248850 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220623 MGI PMID:26162102 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220623 MGI PMID:26248850 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220721 MGI PMID:26853561 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220623 MGI PMID:26162102 1557906 Rfx2 regulatory factor X, 2 (influences HLA class II expression) gene MP:0031389 abnormal ectoplasmic specialization morphology IAGP N RGD:5509061 20220623 MGI PMID:26162102 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20220811 MGI 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20220811 MGI 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0020337 abnormal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557907 Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20190321 MGI PMID:30318146 1557910 Slc6a11 solute carrier family 6 (neurotransmitter transporter, GABA), member 11 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20111116 MGI 1557910 Slc6a11 solute carrier family 6 (neurotransmitter transporter, GABA), member 11 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1557912 Ifitm3 interferon induced transmembrane protein 3 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:24278312 1557912 Ifitm3 interferon induced transmembrane protein 3 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:22446628 1557912 Ifitm3 interferon induced transmembrane protein 3 gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:22446628 1557915 Acer1 alkaline ceramidase 1 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20180301 MGI PMID:29056331 1557915 Acer1 alkaline ceramidase 1 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20180301 MGI PMID:29056331 1557915 Acer1 alkaline ceramidase 1 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20180301 MGI PMID:29056331 1557915 Acer1 alkaline ceramidase 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1557915 Acer1 alkaline ceramidase 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0002992 abnormal sebaceous lipid secretion IAGP N RGD:5509061 20180301 MGI PMID:29056331 1557915 Acer1 alkaline ceramidase 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0003853 dry skin IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20180301 MGI PMID:29056331 1557915 Acer1 alkaline ceramidase 1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20180301 MGI PMID:29056331 1557915 Acer1 alkaline ceramidase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180301 MGI PMID:29056331 1557915 Acer1 alkaline ceramidase 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20180301 MGI PMID:29056331 1557915 Acer1 alkaline ceramidase 1 gene MP:0008860 abnormal hair cycle telogen phase IAGP N RGD:5509061 20180301 MGI PMID:29056331 1557915 Acer1 alkaline ceramidase 1 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0009441 delayed skin barrier formation IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0009535 abnormal skin sebaceous gland morphology IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0009602 abnormal keratohyalin granule morphology IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0009759 abnormal hair follicle bulge morphology IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0009793 sebaceous gland hypertrophy IAGP N RGD:5509061 20180301 MGI PMID:29056331 1557915 Acer1 alkaline ceramidase 1 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0010682 abnormal hair follicle infundibulum morphology IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0010683 dilated hair follicle infundibulum IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0010683 dilated hair follicle infundibulum IAGP N RGD:5509061 20180301 MGI PMID:29056331 1557915 Acer1 alkaline ceramidase 1 gene MP:0011194 abnormal hair follicle physiology IAGP N RGD:5509061 20180301 MGI PMID:29056331 1557915 Acer1 alkaline ceramidase 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0013375 abnormal sebocyte morphology IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0020117 decreased sphingosine level IAGP N RGD:5509061 20161117 MGI PMID:27126290 1557915 Acer1 alkaline ceramidase 1 gene MP:0030570 abnormal piliary canal morphology IAGP N RGD:5509061 20180524 MGI PMID:29056331 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15489218 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16223892 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:11875044 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15489218 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16223892 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15489218 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11875044 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20141003 MGI 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0001304 cataract IEA N RGD:5509061 20141003 MGI 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:16223892 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16223892 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11875044 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15489218 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:16223892 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:11875044 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16223892 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15489218 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:9418970 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9126326 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9256488 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9418970 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12719378 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160915 MGI PMID:24652767 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15489218 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16223892 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:11875044 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:16223892 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:15489218 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:15489218 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:16223892 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15489218 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15489218 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16223892 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20180830 MGI PMID:27124591 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0005284 increased saturated fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:9256488 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:11875044 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:15489218 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:11875044 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:15489218 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15489218 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0008294 abnormal adrenal gland zona fasciculata morphology IAGP N RGD:5509061 20141003 MGI PMID:15489218 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0008295 abnormal adrenal gland zona reticularis morphology IAGP N RGD:5509061 20141003 MGI PMID:15489218 1557916 Abcd1 ATP-binding cassette, sub-family D member 1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20180920 MGI PMID:27124591 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0009848 increased horizontal stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0009849 increased vertical stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:21775500 1557918 Zdhhc17 zinc finger, DHHC domain containing 17 gene MP:0020083 decreased hippocampus volume IAGP N RGD:5509061 20170706 MGI PMID:21775500 1557919 Dnm3 dynamin 3 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:21689597 1557919 Dnm3 dynamin 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:21689597 1557919 Dnm3 dynamin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21689597 1557919 Dnm3 dynamin 3 gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20141003 MGI PMID:21689597 1557919 Dnm3 dynamin 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21689597 1557919 Dnm3 dynamin 3 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:21689597 1557919 Dnm3 dynamin 3 gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:21689597 1557919 Dnm3 dynamin 3 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:21689597 1557919 Dnm3 dynamin 3 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:21689597 1557919 Dnm3 dynamin 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21689597 1557919 Dnm3 dynamin 3 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:21689597 1557922 Magee2 MAGE family member E2 gene MP:0000434 megacephaly IAGP N RGD:5509061 20221222 MGI PMID:34464968 1557922 Magee2 MAGE family member E2 gene MP:0000905 increased superior colliculus size IAGP N RGD:5509061 20221222 MGI PMID:34464968 1557922 Magee2 MAGE family member E2 gene MP:0005238 increased brain size IAGP N RGD:5509061 20221222 MGI PMID:34464968 1557922 Magee2 MAGE family member E2 gene MP:0008228 increased anterior commissure size IAGP N RGD:5509061 20221222 MGI PMID:34464968 1557922 Magee2 MAGE family member E2 gene MP:0012449 increased primary motor cortex size IAGP N RGD:5509061 20221222 MGI PMID:34464968 1557922 Magee2 MAGE family member E2 gene MP:0012451 abnormal retrosplenial granular cortex morphology IAGP N RGD:5509061 20221222 MGI PMID:34464968 1557922 Magee2 MAGE family member E2 gene MP:0012452 increased retrosplenial granular cortex size IAGP N RGD:5509061 20221222 MGI PMID:34464968 1557922 Magee2 MAGE family member E2 gene MP:0012465 increased hippocampal fimbria size IAGP N RGD:5509061 20221222 MGI PMID:34464968 1557922 Magee2 MAGE family member E2 gene MP:0020534 increased pons size IAGP N RGD:5509061 20221222 MGI PMID:34464968 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000084 abnormal fontanelle morphology IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000423 delayed hair regrowth IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20210826 MGI 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220519 MGI PMID:31489491 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20220519 MGI PMID:31489491 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10691732 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10691732 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19504344 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:19504344 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:19504344 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20220519 MGI PMID:31489491 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160421 MGI 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0008404 increased cellular sensitivity to methylmethanesulfonate IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0009362 abnormal primary ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0009794 sebaceous gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0009949 abnormal olfactory bulb granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10691732 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10801416 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0011120 increased primordial ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:31489491 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:31489491 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20141003 MGI PMID:18371340 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0011496 abnormal head size IAGP N RGD:5509061 20141003 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0012525 abnormal rhombic lip morphology IAGP N RGD:5509061 20141003 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20220519 MGI PMID:31489491 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0013551 decreased cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20161201 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0030004 hippocampus hypoplasia IAGP N RGD:5509061 20170706 MGI PMID:22266795 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0030048 sloping forehead IAGP N RGD:5509061 20170921 MGI PMID:19620979 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0031018 decreased granulosa cell proliferation IAGP N RGD:5509061 20220519 MGI PMID:31489491 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0031019 increased granulosa cell proliferation IAGP N RGD:5509061 20220519 MGI PMID:31489491 1557923 Atr ataxia telangiectasia and Rad3 related gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:31489491 1557925 Rspo4 R-spondin 4 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20221110 MGI 1557926 Krt16 keratin 16 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22336941 1557926 Krt16 keratin 16 gene MP:0000763 abnormal filiform papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:22336941 1557926 Krt16 keratin 16 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22336941 1557926 Krt16 keratin 16 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:22336941 1557926 Krt16 keratin 16 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:22336941 1557926 Krt16 keratin 16 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:22336941 1557926 Krt16 keratin 16 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22336941 1557926 Krt16 keratin 16 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22336941 1557926 Krt16 keratin 16 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22336941 1557926 Krt16 keratin 16 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:22336941 1557926 Krt16 keratin 16 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:22336941 1557926 Krt16 keratin 16 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22336941 1557926 Krt16 keratin 16 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22336941 1557927 Eif3c eukaryotic translation initiation factor 3, subunit C gene MP:0000373 belly spot IEA N RGD:5509061 20111116 MGI 1557927 Eif3c eukaryotic translation initiation factor 3, subunit C gene MP:0000562 polydactyly IEA N RGD:5509061 20111116 MGI 1557927 Eif3c eukaryotic translation initiation factor 3, subunit C gene MP:0001732 postnatal growth retardation IEA N RGD:5509061 20111116 MGI 1557927 Eif3c eukaryotic translation initiation factor 3, subunit C gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20111116 MGI 1557927 Eif3c eukaryotic translation initiation factor 3, subunit C gene MP:0002177 abnormal outer ear morphology IEA N RGD:5509061 20111116 MGI 1557927 Eif3c eukaryotic translation initiation factor 3, subunit C gene MP:0002938 white spotting IEA N RGD:5509061 20111116 MGI 1557927 Eif3c eukaryotic translation initiation factor 3, subunit C gene MP:0002939 head spot IEA N RGD:5509061 20111116 MGI 1557927 Eif3c eukaryotic translation initiation factor 3, subunit C gene MP:0008770 decreased survivor rate IEA N RGD:5509061 20111116 MGI 1557927 Eif3c eukaryotic translation initiation factor 3, subunit C gene MP:0009049 abnormal hallux morphology IEA N RGD:5509061 20111116 MGI 1557928 Zdhhc8 zinc finger, DHHC domain containing 8 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:15184899 1557928 Zdhhc8 zinc finger, DHHC domain containing 8 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20160526 MGI PMID:18836441 1557928 Zdhhc8 zinc finger, DHHC domain containing 8 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:15184899 1557928 Zdhhc8 zinc finger, DHHC domain containing 8 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20160526 MGI PMID:18836441 1557928 Zdhhc8 zinc finger, DHHC domain containing 8 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20160526 MGI PMID:18836441 1557929 Rnf208 ring finger protein 208 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1557929 Rnf208 ring finger protein 208 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1557929 Rnf208 ring finger protein 208 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1557929 Rnf208 ring finger protein 208 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 1557929 Rnf208 ring finger protein 208 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 1557929 Rnf208 ring finger protein 208 gene MP:0001262 decreased body weight IEA N RGD:5509061 20220519 MGI 1557929 Rnf208 ring finger protein 208 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1557929 Rnf208 ring finger protein 208 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1557929 Rnf208 ring finger protein 208 gene MP:0004156 abnormal QT variability IEA N RGD:5509061 20220519 MGI 1557929 Rnf208 ring finger protein 208 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20220811 MGI 1557929 Rnf208 ring finger protein 208 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20210826 MGI 1557929 Rnf208 ring finger protein 208 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1557929 Rnf208 ring finger protein 208 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20210826 MGI 1557929 Rnf208 ring finger protein 208 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210826 MGI 1557929 Rnf208 ring finger protein 208 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20240627 MGI 1557929 Rnf208 ring finger protein 208 gene MP:0011047 increased lung tissue damping IEA N RGD:5509061 20220519 MGI 1557931 Fbxo41 F-box protein 41 gene MP:0000745 tremors IAGP N RGD:5509061 20160630 MGI PMID:26063905 1557931 Fbxo41 F-box protein 41 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20160630 MGI PMID:26063905 1557931 Fbxo41 F-box protein 41 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20160630 MGI PMID:26063905 1557931 Fbxo41 F-box protein 41 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20160630 MGI PMID:26063905 1557931 Fbxo41 F-box protein 41 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160630 MGI PMID:26063905 1557931 Fbxo41 F-box protein 41 gene MP:0001393 ataxia IAGP N RGD:5509061 20160630 MGI PMID:26063905 1557931 Fbxo41 F-box protein 41 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1557931 Fbxo41 F-box protein 41 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160630 MGI PMID:26063905 1557931 Fbxo41 F-box protein 41 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160630 MGI PMID:26063905 1557931 Fbxo41 F-box protein 41 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1557931 Fbxo41 F-box protein 41 gene MP:0001513 limb grasping IAGP N RGD:5509061 20160630 MGI PMID:26063905 1557931 Fbxo41 F-box protein 41 gene MP:0001525 impaired balance IAGP N RGD:5509061 20160630 MGI PMID:26063905 1557931 Fbxo41 F-box protein 41 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160630 MGI PMID:26063905 1557931 Fbxo41 F-box protein 41 gene MP:0002083 premature death IAGP N RGD:5509061 20160630 MGI PMID:26063905 1557931 Fbxo41 F-box protein 41 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20160630 MGI PMID:26063905 1557931 Fbxo41 F-box protein 41 gene MP:0002833 increased heart weight IEA N RGD:5509061 20231207 MGI 1557931 Fbxo41 F-box protein 41 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20210128 MGI 1557931 Fbxo41 F-box protein 41 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1557931 Fbxo41 F-box protein 41 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 1557931 Fbxo41 F-box protein 41 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20160630 MGI PMID:26063905 1557931 Fbxo41 F-box protein 41 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20231207 MGI 1557931 Fbxo41 F-box protein 41 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1557931 Fbxo41 F-box protein 41 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160630 MGI PMID:26063905 1557932 Slc44a1 solute carrier family 44, member 1 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20201231 MGI 1557932 Slc44a1 solute carrier family 44, member 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1557932 Slc44a1 solute carrier family 44, member 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20190502 MGI 1557932 Slc44a1 solute carrier family 44, member 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1557932 Slc44a1 solute carrier family 44, member 1 gene MP:0002626 increased heart rate IEA N RGD:5509061 20230601 MGI 1557932 Slc44a1 solute carrier family 44, member 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210520 MGI 1557932 Slc44a1 solute carrier family 44, member 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1557932 Slc44a1 solute carrier family 44, member 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20201022 MGI 1557932 Slc44a1 solute carrier family 44, member 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1557932 Slc44a1 solute carrier family 44, member 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20190502 MGI 1557932 Slc44a1 solute carrier family 44, member 1 gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20220811 MGI 1557932 Slc44a1 solute carrier family 44, member 1 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20240627 MGI 1557932 Slc44a1 solute carrier family 44, member 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 1557934 Epgn epithelial mitogen gene MP:0001523 impaired righting response IEA N RGD:5509061 20170105 MGI 1557934 Epgn epithelial mitogen gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23142483 1557934 Epgn epithelial mitogen gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:23142483 1557935 Zranb3 zinc finger, RAN-binding domain containing 3 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20231207 MGI 1557936 Tmprss11f transmembrane protease, serine 11f gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20191003 MGI PMID:28338078 1557936 Tmprss11f transmembrane protease, serine 11f gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20191031 MGI PMID:31501243 1557936 Tmprss11f transmembrane protease, serine 11f gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20191003 MGI PMID:28338078 1557937 Fcho2 FCH domain only 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1557937 Fcho2 FCH domain only 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1557937 Fcho2 FCH domain only 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1557937 Fcho2 FCH domain only 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1557937 Fcho2 FCH domain only 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557939 Pdzd4 PDZ domain containing 4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1557941 Kbtbd12 kelch repeat and BTB (POZ) domain containing 12 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20230601 MGI 1557941 Kbtbd12 kelch repeat and BTB (POZ) domain containing 12 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1557941 Kbtbd12 kelch repeat and BTB (POZ) domain containing 12 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1557941 Kbtbd12 kelch repeat and BTB (POZ) domain containing 12 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20230601 MGI 1557943 Pld4 phospholipase D family member 4 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1557943 Pld4 phospholipase D family member 4 gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220519 MGI 1557943 Pld4 phospholipase D family member 4 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0000416 sparse hair IEA N RGD:5509061 20120126 MGI 1557943 Pld4 phospholipase D family member 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1557943 Pld4 phospholipase D family member 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20190905 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20190905 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20190905 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190905 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160929 MGI PMID:27534441 1557943 Pld4 phospholipase D family member 4 gene MP:0001314 cornea opacity IEA N RGD:5509061 20210520 MGI 1557943 Pld4 phospholipase D family member 4 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20190926 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20190926 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20190926 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20190926 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20190926 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20190905 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210520 MGI 1557943 Pld4 phospholipase D family member 4 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20240523 MGI 1557943 Pld4 phospholipase D family member 4 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20190926 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210520 MGI 1557943 Pld4 phospholipase D family member 4 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20190926 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20190905 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20190905 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0008244 abnormal peritoneal macrophage morphology IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20190905 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20190926 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20190926 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0008524 increased plasmacytoid dendritic cell number IAGP N RGD:5509061 20190926 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0012762 abnormal alpha-beta T cell morphology IAGP N RGD:5509061 20190926 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20190926 MGI PMID:30679154 1557943 Pld4 phospholipase D family member 4 gene MP:0031070 hemophagocytosis IAGP N RGD:5509061 20200910 MGI PMID:30111894 1557943 Pld4 phospholipase D family member 4 gene MP:0031220 increased circulating CXCL10 level IAGP N RGD:5509061 20210204 MGI PMID:30111894 1557944 Tnrc6a trinucleotide repeat containing 6a gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20160304 MGI PMID:22187428 1557944 Tnrc6a trinucleotide repeat containing 6a gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20160304 MGI PMID:22187428 1557944 Tnrc6a trinucleotide repeat containing 6a gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20160304 MGI PMID:22187428 1557944 Tnrc6a trinucleotide repeat containing 6a gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20160304 MGI PMID:22187428 1557944 Tnrc6a trinucleotide repeat containing 6a gene MP:0003717 pallor IAGP N RGD:5509061 20160304 MGI PMID:22187428 1557944 Tnrc6a trinucleotide repeat containing 6a gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180315 MGI PMID:28811219 1557944 Tnrc6a trinucleotide repeat containing 6a gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20160304 MGI PMID:22187428 1557944 Tnrc6a trinucleotide repeat containing 6a gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20160304 MGI PMID:22187428 1557944 Tnrc6a trinucleotide repeat containing 6a gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20160304 MGI PMID:22187428 1557946 Myg1 melanocyte proliferating gene 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:19818808 1557946 Myg1 melanocyte proliferating gene 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19818808 1557946 Myg1 melanocyte proliferating gene 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:19818808 1557946 Myg1 melanocyte proliferating gene 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19818808 1557946 Myg1 melanocyte proliferating gene 1 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:19818808 1557946 Myg1 melanocyte proliferating gene 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:19818808 1557946 Myg1 melanocyte proliferating gene 1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:19818808 1557946 Myg1 melanocyte proliferating gene 1 gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:19818808 1557947 Abca16 ATP-binding cassette, sub-family A member 16 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201022 MGI 1557947 Abca16 ATP-binding cassette, sub-family A member 16 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210826 MGI 1557947 Abca16 ATP-binding cassette, sub-family A member 16 gene MP:0001513 limb grasping IEA N RGD:5509061 20201231 MGI 1557947 Abca16 ATP-binding cassette, sub-family A member 16 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 1557947 Abca16 ATP-binding cassette, sub-family A member 16 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20230601 MGI 1557947 Abca16 ATP-binding cassette, sub-family A member 16 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1557948 Phf6 PHD finger protein 6 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20210304 MGI PMID:32994169 1557948 Phf6 PHD finger protein 6 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0001258 decreased body length IAGP N RGD:5509061 20190516 MGI PMID:30403997 1557948 Phf6 PHD finger protein 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190516 MGI PMID:30403997 1557948 Phf6 PHD finger protein 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210304 MGI PMID:32994169 1557948 Phf6 PHD finger protein 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210304 MGI PMID:32994169 1557948 Phf6 PHD finger protein 6 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20190516 MGI PMID:30403997 1557948 Phf6 PHD finger protein 6 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20190516 MGI PMID:30403997 1557948 Phf6 PHD finger protein 6 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20190516 MGI PMID:30403997 1557948 Phf6 PHD finger protein 6 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20210304 MGI PMID:30755422 1557948 Phf6 PHD finger protein 6 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20210304 MGI PMID:30755422 1557948 Phf6 PHD finger protein 6 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20210304 MGI PMID:30755422 1557948 Phf6 PHD finger protein 6 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20190516 MGI PMID:30403997 1557948 Phf6 PHD finger protein 6 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20190516 MGI PMID:30403997 1557948 Phf6 PHD finger protein 6 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0003466 decreased single cell response threshold IAGP N RGD:5509061 20190516 MGI PMID:30403997 1557948 Phf6 PHD finger protein 6 gene MP:0003468 increased single cell response intensity IAGP N RGD:5509061 20190516 MGI PMID:30403997 1557948 Phf6 PHD finger protein 6 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20210304 MGI PMID:32994169 1557948 Phf6 PHD finger protein 6 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20210304 MGI PMID:32994169 1557948 Phf6 PHD finger protein 6 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1557948 Phf6 PHD finger protein 6 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20210304 MGI PMID:30755422 1557948 Phf6 PHD finger protein 6 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20210304 MGI PMID:30755422 1557948 Phf6 PHD finger protein 6 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20190516 MGI PMID:30403997 1557948 Phf6 PHD finger protein 6 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20210304 MGI PMID:32994169 1557948 Phf6 PHD finger protein 6 gene MP:0005128 decreased adrenocorticotropin level IAGP N RGD:5509061 20210304 MGI PMID:32994169 1557948 Phf6 PHD finger protein 6 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20210304 MGI PMID:32994169 1557948 Phf6 PHD finger protein 6 gene MP:0005138 decreased prolactin level IAGP N RGD:5509061 20210304 MGI PMID:32994169 1557948 Phf6 PHD finger protein 6 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20210304 MGI PMID:32994169 1557948 Phf6 PHD finger protein 6 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20190516 MGI PMID:30403997 1557948 Phf6 PHD finger protein 6 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0008524 increased plasmacytoid dendritic cell number IAGP N RGD:5509061 20210304 MGI PMID:30755422 1557948 Phf6 PHD finger protein 6 gene MP:0008573 increased circulating interferon-alpha level IAGP N RGD:5509061 20210304 MGI PMID:30755422 1557948 Phf6 PHD finger protein 6 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20190516 MGI PMID:30403997 1557948 Phf6 PHD finger protein 6 gene MP:0010132 decreased DN2 thymocyte number IAGP N RGD:5509061 20210304 MGI PMID:30755422 1557948 Phf6 PHD finger protein 6 gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210304 MGI PMID:32994169 1557948 Phf6 PHD finger protein 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20190516 MGI PMID:30403997 1557948 Phf6 PHD finger protein 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20210304 MGI PMID:30755422 1557948 Phf6 PHD finger protein 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20210304 MGI PMID:32994169 1557948 Phf6 PHD finger protein 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557948 Phf6 PHD finger protein 6 gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20210304 MGI PMID:30755422 1557948 Phf6 PHD finger protein 6 gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0013707 abnormal hematopoietic precursor cell morphology IAGP N RGD:5509061 20210304 MGI PMID:30755422 1557948 Phf6 PHD finger protein 6 gene MP:0013762 abnormal effector T cell number IAGP N RGD:5509061 20220609 MGI PMID:31395598 1557948 Phf6 PHD finger protein 6 gene MP:0013892 increased common lymphocyte progenitor cell number IAGP N RGD:5509061 20210304 MGI PMID:30755422 1557948 Phf6 PHD finger protein 6 gene MP:0014400 increased hematopoietic precursor cell number IAGP N RGD:5509061 20240321 MGI PMID:30755422 1557948 Phf6 PHD finger protein 6 gene MP:0020396 abnormal social recognition IAGP N RGD:5509061 20190516 MGI PMID:30403997 1557949 Shroom3 shroom family member 3 gene MP:0000075 absent neurocranium IAGP N RGD:5509061 20141003 MGI PMID:10589677 1557949 Shroom3 shroom family member 3 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:10589677 1557949 Shroom3 shroom family member 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231207 MGI PMID:32511952 1557949 Shroom3 shroom family member 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20231207 MGI PMID:32511952 1557949 Shroom3 shroom family member 3 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231207 MGI PMID:32511952 1557949 Shroom3 shroom family member 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10589677 1557949 Shroom3 shroom family member 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10589677 1557949 Shroom3 shroom family member 3 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:10589677 1557949 Shroom3 shroom family member 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20221215 MGI 1557949 Shroom3 shroom family member 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:10589677 1557949 Shroom3 shroom family member 3 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20221215 MGI 1557949 Shroom3 shroom family member 3 gene MP:0003054 spina bifida IEA N RGD:5509061 20221215 MGI 1557949 Shroom3 shroom family member 3 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20111116 MGI 1557949 Shroom3 shroom family member 3 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20221215 MGI 1557949 Shroom3 shroom family member 3 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20231207 MGI PMID:32511952 1557949 Shroom3 shroom family member 3 gene MP:0005155 herniated intestine IAGP N RGD:5509061 20141003 MGI PMID:10589677 1557949 Shroom3 shroom family member 3 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231207 MGI PMID:32511952 1557949 Shroom3 shroom family member 3 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20231207 MGI PMID:32511952 1557949 Shroom3 shroom family member 3 gene MP:0008797 facial cleft IEA N RGD:5509061 20111116 MGI 1557949 Shroom3 shroom family member 3 gene MP:0009908 protruding tongue IEA N RGD:5509061 20221215 MGI 1557949 Shroom3 shroom family member 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231207 MGI PMID:32511952 1557949 Shroom3 shroom family member 3 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20231207 MGI PMID:32511952 1557949 Shroom3 shroom family member 3 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20231207 MGI PMID:32511952 1557949 Shroom3 shroom family member 3 gene MP:0010433 double inlet heart left ventricle IAGP N RGD:5509061 20231207 MGI PMID:32511952 1557949 Shroom3 shroom family member 3 gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20231207 MGI PMID:32511952 1557949 Shroom3 shroom family member 3 gene MP:0010912 herniated liver IAGP N RGD:5509061 20141003 MGI PMID:10589677 1557949 Shroom3 shroom family member 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10589677 1557949 Shroom3 shroom family member 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1557949 Shroom3 shroom family member 3 gene MP:0011394 increased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20231207 MGI PMID:32511952 1557949 Shroom3 shroom family member 3 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20231207 MGI PMID:32511952 1557949 Shroom3 shroom family member 3 gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231207 MGI PMID:32511952 1557949 Shroom3 shroom family member 3 gene MP:0031525 thin left ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:32511952 1557951 Rpe ribulose-5-phosphate-3-epimerase gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1557951 Rpe ribulose-5-phosphate-3-epimerase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1557951 Rpe ribulose-5-phosphate-3-epimerase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1557951 Rpe ribulose-5-phosphate-3-epimerase gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1557951 Rpe ribulose-5-phosphate-3-epimerase gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1557951 Rpe ribulose-5-phosphate-3-epimerase gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1557951 Rpe ribulose-5-phosphate-3-epimerase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1557951 Rpe ribulose-5-phosphate-3-epimerase gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1557951 Rpe ribulose-5-phosphate-3-epimerase gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 1557951 Rpe ribulose-5-phosphate-3-epimerase gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1557951 Rpe ribulose-5-phosphate-3-epimerase gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 1557951 Rpe ribulose-5-phosphate-3-epimerase gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210128 MGI 1557951 Rpe ribulose-5-phosphate-3-epimerase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557951 Rpe ribulose-5-phosphate-3-epimerase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1557951 Rpe ribulose-5-phosphate-3-epimerase gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 1557952 Ehd2 EH-domain containing 2 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20200402 MGI 1557952 Ehd2 EH-domain containing 2 gene MP:0005666 abnormal adipose tissue physiology IEA N RGD:5509061 20200402 MGI 1557952 Ehd2 EH-domain containing 2 gene MP:0009117 abnormal white fat cell morphology IEA N RGD:5509061 20200402 MGI 1557952 Ehd2 EH-domain containing 2 gene MP:0009118 increased white fat cell size IEA N RGD:5509061 20200402 MGI 1557952 Ehd2 EH-domain containing 2 gene MP:0009121 increased white fat cell lipid droplet size IEA N RGD:5509061 20200402 MGI 1557952 Ehd2 EH-domain containing 2 gene MP:0009124 increased brown fat cell lipid droplet size IEA N RGD:5509061 20200402 MGI 1557952 Ehd2 EH-domain containing 2 gene MP:0009285 increased gonadal fat pad weight IEA N RGD:5509061 20200402 MGI 1557952 Ehd2 EH-domain containing 2 gene MP:0009292 increased inguinal fat pad weight IEA N RGD:5509061 20200402 MGI 1557952 Ehd2 EH-domain containing 2 gene MP:0020325 abnormal beige fat cell morphology IEA N RGD:5509061 20200402 MGI 1557952 Ehd2 EH-domain containing 2 gene MP:0020414 abnormal fibroblast physiology IEA N RGD:5509061 20200402 MGI 1557952 Ehd2 EH-domain containing 2 gene MP:0030016 increased adipocyte glucose uptake IEA N RGD:5509061 20200402 MGI 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20231207 MGI 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20191003 MGI PMID:28290521 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210826 MGI 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20191003 MGI PMID:28290521 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20191003 MGI PMID:28290521 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20191003 MGI PMID:28290521 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20191003 MGI PMID:28290521 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20191003 MGI PMID:28290521 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1557954 Ndrg3 N-myc downstream regulated gene 3 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20220811 MGI 1557957 Atp5f1b ATP synthase F1 subunit beta gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230720 MGI 1557957 Atp5f1b ATP synthase F1 subunit beta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230720 MGI 1557957 Atp5f1b ATP synthase F1 subunit beta gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230720 MGI 1557957 Atp5f1b ATP synthase F1 subunit beta gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20230720 MGI 1557958 Gipr gastric inhibitory polypeptide receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:10611300 1557958 Gipr gastric inhibitory polypeptide receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10611300 1557958 Gipr gastric inhibitory polypeptide receptor gene MP:0002694 abnormal pancreas secretion IAGP N RGD:5509061 20141003 MGI PMID:14966573 1557958 Gipr gastric inhibitory polypeptide receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10611300 1557958 Gipr gastric inhibitory polypeptide receptor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14966573 1557958 Gipr gastric inhibitory polypeptide receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:14966573 1557958 Gipr gastric inhibitory polypeptide receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:14966573 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0004038 lymphangiectasis IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20713964 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20210128 MGI 1557960 Lpar4 lysophosphatidic acid receptor 4 gene MP:0014273 abnormal skin vasculature morphology IAGP N RGD:5509061 20230810 MGI PMID:20713964 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200514 MGI PMID:31416892 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20200514 MGI PMID:31416892 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200514 MGI PMID:31416892 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200514 MGI PMID:31416892 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200514 MGI PMID:31416892 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20200514 MGI PMID:31416892 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20200514 MGI PMID:31416892 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0008431 abnormal short-term spatial reference memory IAGP N RGD:5509061 20200514 MGI PMID:31416892 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20190221 MGI PMID:26246171 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20190221 MGI PMID:26246171 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20190221 MGI PMID:26246171 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20200514 MGI PMID:31416892 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20200514 MGI PMID:31416892 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0011637 abnormal mitochondrial matrix morphology IAGP N RGD:5509061 20200514 MGI PMID:31416892 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20200514 MGI PMID:31416892 1557961 Marchf5 membrane associated ring-CH-type finger 5 gene MP:0031023 decreased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:26246171 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:21606200 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:21606200 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:21606200 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21606200 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:21606200 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:21606200 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21606200 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20141003 MGI PMID:21606200 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0011522 abnormal placental labyrinth villi morphology IAGP N RGD:5509061 20141003 MGI PMID:21606200 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0011525 abnormal placenta intervillous maternal lacunae morphology IAGP N RGD:5509061 20141003 MGI PMID:21606200 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0011526 abnormal placenta fetal blood space morphology IAGP N RGD:5509061 20141003 MGI PMID:21606200 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0011528 abnormal placental labyrinth villi branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:21606200 1557962 Llgl2 LLGL2 scribble cell polarity complex component gene MP:0011529 increased placenta intervillous maternal lacunae size IAGP N RGD:5509061 20141003 MGI PMID:21606200 1557963 Hoxb4 homeobox B4 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9012503 1557963 Hoxb4 homeobox B4 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:14962901 1557963 Hoxb4 homeobox B4 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14962901 1557963 Hoxb4 homeobox B4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8097432 1557963 Hoxb4 homeobox B4 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9012503 1557963 Hoxb4 homeobox B4 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14962901 1557963 Hoxb4 homeobox B4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12748289 1557963 Hoxb4 homeobox B4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14962901 1557963 Hoxb4 homeobox B4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21278354 1557963 Hoxb4 homeobox B4 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:14962901 1557963 Hoxb4 homeobox B4 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14962901 1557963 Hoxb4 homeobox B4 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7628700 1557963 Hoxb4 homeobox B4 gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:9012503 1557963 Hoxb4 homeobox B4 gene MP:0003385 abnormal body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0003388 absent pericardium IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:8097432 1557963 Hoxb4 homeobox B4 gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20141003 MGI PMID:8097432 1557963 Hoxb4 homeobox B4 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:8097432 1557963 Hoxb4 homeobox B4 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:8097432 1557963 Hoxb4 homeobox B4 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:9012503 1557963 Hoxb4 homeobox B4 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:8097432 1557963 Hoxb4 homeobox B4 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:7628700 1557963 Hoxb4 homeobox B4 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7628700 1557963 Hoxb4 homeobox B4 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:8097432 1557963 Hoxb4 homeobox B4 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9012503 1557963 Hoxb4 homeobox B4 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:7628700 1557963 Hoxb4 homeobox B4 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:8097432 1557963 Hoxb4 homeobox B4 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7628700 1557963 Hoxb4 homeobox B4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7628700 1557963 Hoxb4 homeobox B4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8097432 1557963 Hoxb4 homeobox B4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11518511 1557963 Hoxb4 homeobox B4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9012503 1557963 Hoxb4 homeobox B4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8097432 1557964 Il16 interleukin 16 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15728482 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16625202 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16714379 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16625202 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:16714379 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20211202 MGI PMID:28031478 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:16714379 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:16625202 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:16625202 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16714379 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20210128 MGI 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20150312 MGI PMID:24530055 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16625202 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16714379 1557966 Ifih1 interferon induced with helicase C domain 1 gene MP:0031301 chronic liver inflammation IAGP N RGD:5509061 20211028 MGI PMID:24530055 1557967 Vps37a vacuolar protein sorting 37A gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20230119 MGI 1557967 Vps37a vacuolar protein sorting 37A gene MP:0001258 decreased body length IEA N RGD:5509061 20230119 MGI 1557967 Vps37a vacuolar protein sorting 37A gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230119 MGI 1557967 Vps37a vacuolar protein sorting 37A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1557967 Vps37a vacuolar protein sorting 37A gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230119 MGI 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:23533672 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:23533672 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23533672 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18026105 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23533672 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:23533672 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23533672 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23533672 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18026105 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:23533672 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:23533672 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:23533672 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:23533672 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:23533672 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:23533672 1557969 Rgs13 regulator of G-protein signaling 13 gene MP:0008896 increased IgG2c level IAGP N RGD:5509061 20141003 MGI PMID:23533672 1557971 Nkx1-1 NK1 homeobox 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14645517 1557971 Nkx1-1 NK1 homeobox 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:14645517 1557971 Nkx1-1 NK1 homeobox 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:14645517 1557971 Nkx1-1 NK1 homeobox 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14645517 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20160616 MGI PMID:24876128 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:17242199 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20160616 MGI PMID:24876128 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17242199 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:17242199 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17242199 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20160616 MGI PMID:24876128 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17242199 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17242199 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17242199 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20160616 MGI PMID:24876128 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17242199 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17242199 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20160616 MGI PMID:24876128 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0009137 decreased brown fat lipid droplet number IAGP N RGD:5509061 20160616 MGI PMID:24876128 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:17242199 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:17242199 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20160616 MGI PMID:24876128 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0011170 abnormal brown fat cell differentiation IAGP N RGD:5509061 20160616 MGI PMID:24876128 1557972 Taf7l TATA-box binding protein associated factor 7 like gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20160616 MGI PMID:24876128 1557973 Iqsec3 IQ motif and Sec7 domain 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20201022 MGI 1557973 Iqsec3 IQ motif and Sec7 domain 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20201022 MGI 1557973 Iqsec3 IQ motif and Sec7 domain 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1557973 Iqsec3 IQ motif and Sec7 domain 3 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1557973 Iqsec3 IQ motif and Sec7 domain 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20190502 MGI 1557973 Iqsec3 IQ motif and Sec7 domain 3 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1557973 Iqsec3 IQ motif and Sec7 domain 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1557973 Iqsec3 IQ motif and Sec7 domain 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20190502 MGI 1557973 Iqsec3 IQ motif and Sec7 domain 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20190502 MGI 1557973 Iqsec3 IQ motif and Sec7 domain 3 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1557973 Iqsec3 IQ motif and Sec7 domain 3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1557973 Iqsec3 IQ motif and Sec7 domain 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20231207 MGI 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20230601 MGI 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20231207 MGI 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21412262 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20151119 MGI PMID:22716256 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20151119 MGI PMID:22716256 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0003195 calcinosis IAGP N RGD:5509061 20151119 MGI PMID:22716256 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0010178 increased number of Howell-Jolly bodies IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0011176 abnormal erythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0012563 increased tumor incidence following infection IAGP N RGD:5509061 20141003 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:24029230 1557974 Samd9l sterile alpha motif domain containing 9-like gene MP:0030025 giant platelets IAGP N RGD:5509061 20170803 MGI PMID:24029230 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:16751419 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:12065839 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:8388689 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:10620608 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:11285306 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:1910207 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:1910207 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9491996 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:16709807 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:10078545 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:14570980 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:8388689 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:10078545 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:14570980 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:16751419 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:16751419 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:14570980 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:10620608 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:11285306 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:14570980 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14570980 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:2358682 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11687799 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23712430 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11857806 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12198548 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19917682 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23772037 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11285306 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12507777 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7547694 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002454 abnormal macrophage antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:7547694 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:23712430 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23772037 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7547694 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:2358682 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:1910207 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002726 abnormal pulmonary vein morphology IAGP N RGD:5509061 20141003 MGI PMID:14570980 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:14570980 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:2358682 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:9164958 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:14570980 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003410 abnormal artery development IAGP N RGD:5509061 20141003 MGI PMID:17717295 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003504 thyroid gland inflammation IEA N RGD:5509061 20111116 MGI 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:2358682 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:16751419 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:12065839 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:22561606 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:23772037 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:16751419 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003901 abnormal PR interval IAGP N RGD:5509061 20141003 MGI PMID:16751419 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:20360383 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20180322 MGI PMID:29472249 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:7547694 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:8258349 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:14570980 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:2358682 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:2358682 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0004797 increased anti-erythrocyte antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:8388689 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:23772037 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10620608 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:11285306 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:11285306 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20180322 MGI PMID:29472249 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0004824 decreased susceptibility to experimental autoimmune myasthenia gravis IAGP N RGD:5509061 20141003 MGI PMID:3917973 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:19597498 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23712430 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11285306 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:2358682 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:15653504 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9164958 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9627126 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9164958 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:2358682 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:6948771 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:9491996 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:8388689 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005122 increased circulating thyroid-stimulating hormone level IEA N RGD:5509061 20111116 MGI 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:10078545 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:12507777 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005355 enlarged thyroid gland IEA N RGD:5509061 20111116 MGI 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10620608 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11285306 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14570980 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:14525595 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:16751419 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0006045 mitral valve regurgitation IAGP N RGD:5509061 20231221 MGI PMID:14570980 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:14570980 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16709807 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18258917 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8388689 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9164958 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17082573 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1910207 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20360383 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:7547694 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9491996 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9885917 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180322 MGI PMID:29472249 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7547694 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17082573 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1910207 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20360383 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9164958 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22561606 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8388689 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9491996 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008397 abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16709807 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9491996 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20141003 MGI PMID:18258917 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19917682 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11285306 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:19917682 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:11285306 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:1909605 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:21179499 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16709807 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0010334 pleural effusion IAGP N RGD:5509061 20141003 MGI PMID:14764740 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:14570980 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:14570980 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:16751419 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0010539 decreased level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:16709807 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16709807 1557975 H2-Ab1 histocompatibility 2, class II antigen A, beta 1 gene MP:0012765 decreased alpha-beta T cell number IAGP N RGD:5509061 20180322 MGI PMID:29472249 1557976 Rapgef5 Rap guanine nucleotide exchange factor (GEF) 5 gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 1557977 Rbp7 retinol binding protein 7, cellular gene MP:0011232 abnormal vitamin A level IAGP N RGD:5509061 20141003 MGI PMID:15870066 1557978 Alpk2 alpha-kinase 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 1557978 Alpk2 alpha-kinase 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1557978 Alpk2 alpha-kinase 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20181227 MGI 1557978 Alpk2 alpha-kinase 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20201022 MGI 1557983 Grm2 glutamate receptor, metabotropic 2 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15619115 1557983 Grm2 glutamate receptor, metabotropic 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15753323 1557983 Grm2 glutamate receptor, metabotropic 2 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:8662555 1557983 Grm2 glutamate receptor, metabotropic 2 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:15753323 1557983 Grm2 glutamate receptor, metabotropic 2 gene MP:0001988 cocaine preference IAGP N RGD:5509061 20141003 MGI PMID:15753323 1557983 Grm2 glutamate receptor, metabotropic 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:15753323 1557983 Grm2 glutamate receptor, metabotropic 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:8662555 1557983 Grm2 glutamate receptor, metabotropic 2 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:24053122 1557983 Grm2 glutamate receptor, metabotropic 2 gene MP:0011987 abnormal GABAergic neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:24053122 1557983 Grm2 glutamate receptor, metabotropic 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:15753323 1557984 Tcf23 transcription factor 23 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20241107 MGI PMID:39014976 1557984 Tcf23 transcription factor 23 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20241107 MGI PMID:39014976 1557984 Tcf23 transcription factor 23 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20241107 MGI PMID:39014976 1557984 Tcf23 transcription factor 23 gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20241107 MGI PMID:39014976 1557984 Tcf23 transcription factor 23 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20241107 MGI PMID:39014976 1557984 Tcf23 transcription factor 23 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20241107 MGI PMID:39014976 1557984 Tcf23 transcription factor 23 gene MP:0004514 dystocia IAGP N RGD:5509061 20241107 MGI PMID:39014976 1557984 Tcf23 transcription factor 23 gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20241107 MGI PMID:39014976 1557984 Tcf23 transcription factor 23 gene MP:0008257 thin myometrium IAGP N RGD:5509061 20241107 MGI PMID:39014976 1557984 Tcf23 transcription factor 23 gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20241107 MGI PMID:39014976 1557984 Tcf23 transcription factor 23 gene MP:0012008 delayed parturition IAGP N RGD:5509061 20241107 MGI PMID:39014976 1557984 Tcf23 transcription factor 23 gene MP:0012699 decreased maternal body weight gain IAGP N RGD:5509061 20241107 MGI PMID:39014976 1557984 Tcf23 transcription factor 23 gene MP:0013258 abnormal extracellular matrix morphology IAGP N RGD:5509061 20241107 MGI PMID:39014976 1557984 Tcf23 transcription factor 23 gene MP:0020253 increased collagen level IAGP N RGD:5509061 20241107 MGI PMID:39014976 1557985 Trub2 TruB pseudouridine (psi) synthase family member 2 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1557985 Trub2 TruB pseudouridine (psi) synthase family member 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1557985 Trub2 TruB pseudouridine (psi) synthase family member 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1557985 Trub2 TruB pseudouridine (psi) synthase family member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:22914734 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22914734 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22914734 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22914734 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22914734 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:22028811 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22028811 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22914734 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:22914734 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22914734 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:22914734 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22914734 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:22914734 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:22914734 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20141003 MGI PMID:22914734 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0008238 abnormal dorsoventral coat patterning IAGP N RGD:5509061 20141003 MGI PMID:18401429 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0010009 abnormal piriform cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22914734 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:22028811 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:22028811 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22028811 1557988 Uqcrfs1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20160421 MGI PMID:22028811 1557990 Dazl deleted in azoospermia-like gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:9288969 1557990 Dazl deleted in azoospermia-like gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9288969 1557990 Dazl deleted in azoospermia-like gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11514340 1557990 Dazl deleted in azoospermia-like gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:9288969 1557990 Dazl deleted in azoospermia-like gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9288969 1557990 Dazl deleted in azoospermia-like gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9288969 1557990 Dazl deleted in azoospermia-like gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11514340 1557990 Dazl deleted in azoospermia-like gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:9288969 1557990 Dazl deleted in azoospermia-like gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:9288969 1557990 Dazl deleted in azoospermia-like gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:9288969 1557990 Dazl deleted in azoospermia-like gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17219433 1557990 Dazl deleted in azoospermia-like gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9288969 1557991 Dlx6 distal-less homeobox 6 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1557991 Dlx6 distal-less homeobox 6 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20171026 MGI PMID:18697905 1557991 Dlx6 distal-less homeobox 6 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12112878 1557991 Dlx6 distal-less homeobox 6 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:12112878 1557991 Dlx6 distal-less homeobox 6 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:18326838 1557991 Dlx6 distal-less homeobox 6 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:12112878 1557991 Dlx6 distal-less homeobox 6 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:12112878 1557991 Dlx6 distal-less homeobox 6 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1557991 Dlx6 distal-less homeobox 6 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12112878 1557991 Dlx6 distal-less homeobox 6 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20171005 MGI PMID:18697905 1557991 Dlx6 distal-less homeobox 6 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0003800 monodactyly IAGP N RGD:5509061 20141003 MGI PMID:18326838 1557991 Dlx6 distal-less homeobox 6 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:12112878 1557991 Dlx6 distal-less homeobox 6 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1557991 Dlx6 distal-less homeobox 6 gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:18697905 1557991 Dlx6 distal-less homeobox 6 gene MP:0004594 abnormal mandibular coronoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0004595 abnormal mandibular condyloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20171019 MGI PMID:18697905 1557991 Dlx6 distal-less homeobox 6 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0005230 ectrodactyly IAGP N RGD:5509061 20141003 MGI PMID:12112878 1557991 Dlx6 distal-less homeobox 6 gene MP:0005230 ectrodactyly IAGP N RGD:5509061 20141003 MGI PMID:18326838 1557991 Dlx6 distal-less homeobox 6 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1557991 Dlx6 distal-less homeobox 6 gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:12112878 1557991 Dlx6 distal-less homeobox 6 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:18326838 1557991 Dlx6 distal-less homeobox 6 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:18697905 1557991 Dlx6 distal-less homeobox 6 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:12112878 1557991 Dlx6 distal-less homeobox 6 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0008380 abnormal gonial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1557991 Dlx6 distal-less homeobox 6 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1557991 Dlx6 distal-less homeobox 6 gene MP:0009917 abnormal hyoid bone body morphology IAGP N RGD:5509061 20141003 MGI PMID:18697905 1557991 Dlx6 distal-less homeobox 6 gene MP:0009918 abnormal stylohyoid ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0010939 abnormal mandibular prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0010994 aerophagia IAGP N RGD:5509061 20141003 MGI PMID:18697905 1557991 Dlx6 distal-less homeobox 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18697905 1557991 Dlx6 distal-less homeobox 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12112878 1557991 Dlx6 distal-less homeobox 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0030259 mandibular condyloid process hypoplasia IAGP N RGD:5509061 20171019 MGI PMID:18697905 1557991 Dlx6 distal-less homeobox 6 gene MP:0030299 lower jaw to upper jaw transformation IAGP N RGD:5509061 20171102 MGI PMID:12434331 1557991 Dlx6 distal-less homeobox 6 gene MP:0030383 small presphenoid bone IAGP N RGD:5509061 20171207 MGI PMID:12434331 1557994 Sptb spectrin beta, erythrocytic gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0000314 schistocytosis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1557994 Sptb spectrin beta, erythrocytic gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:658175 1557994 Sptb spectrin beta, erythrocytic gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0001655 multifocal hepatic necrosis IEA N RGD:5509061 20111116 MGI 1557994 Sptb spectrin beta, erythrocytic gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20240926 MGI 1557994 Sptb spectrin beta, erythrocytic gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0002424 abnormal reticulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:6234993 1557994 Sptb spectrin beta, erythrocytic gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10772878 1557994 Sptb spectrin beta, erythrocytic gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1557994 Sptb spectrin beta, erythrocytic gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0002642 anisocytosis IEA N RGD:5509061 20111116 MGI 1557994 Sptb spectrin beta, erythrocytic gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0002704 tubular nephritis IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0002812 spherocytosis IEA N RGD:5509061 20111116 MGI 1557994 Sptb spectrin beta, erythrocytic gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:10772878 1557994 Sptb spectrin beta, erythrocytic gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0003068 enlarged kidney IEA N RGD:5509061 20111116 MGI 1557994 Sptb spectrin beta, erythrocytic gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0003657 abnormal erythrocyte osmotic lysis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240926 MGI 1557994 Sptb spectrin beta, erythrocytic gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0005360 urolithiasis IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1557994 Sptb spectrin beta, erythrocytic gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0008956 decreased cellular hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0010035 increased erythrocyte clearance IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0010035 increased erythrocyte clearance IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0010163 hemolysis IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0010177 acanthocytosis IEA N RGD:5509061 20111116 MGI 1557994 Sptb spectrin beta, erythrocytic gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6234993 1557994 Sptb spectrin beta, erythrocytic gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6763106 1557994 Sptb spectrin beta, erythrocytic gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20240926 MGI 1557994 Sptb spectrin beta, erythrocytic gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1557994 Sptb spectrin beta, erythrocytic gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1557994 Sptb spectrin beta, erythrocytic gene MP:0011188 increased erythrocyte protoporphyrin level IAGP N RGD:5509061 20141003 MGI PMID:658175 1557994 Sptb spectrin beta, erythrocytic gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20240926 MGI 1557994 Sptb spectrin beta, erythrocytic gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220811 MGI 1557994 Sptb spectrin beta, erythrocytic gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20161124 MGI PMID:10772878 1557994 Sptb spectrin beta, erythrocytic gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20161124 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0021002 brain lesion IAGP N RGD:5509061 20210805 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0021003 cerebral infarct IAGP N RGD:5509061 20210805 MGI PMID:9373273 1557994 Sptb spectrin beta, erythrocytic gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:9373273 1557995 Hoxb8 homeobox B8 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20510925 1557995 Hoxb8 homeobox B8 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:10559485 1557995 Hoxb8 homeobox B8 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:11311170 1557995 Hoxb8 homeobox B8 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:14623233 1557995 Hoxb8 homeobox B8 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:14623233 1557995 Hoxb8 homeobox B8 gene MP:0000155 asymmetric rib joints IAGP N RGD:5509061 20141003 MGI PMID:11311170 1557995 Hoxb8 homeobox B8 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:11311170 1557995 Hoxb8 homeobox B8 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:20510925 1557995 Hoxb8 homeobox B8 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:11311170 1557995 Hoxb8 homeobox B8 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10559485 1557995 Hoxb8 homeobox B8 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10559485 1557995 Hoxb8 homeobox B8 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:11779477 1557995 Hoxb8 homeobox B8 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:10559485 1557995 Hoxb8 homeobox B8 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:20510925 1557995 Hoxb8 homeobox B8 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10559485 1557995 Hoxb8 homeobox B8 gene MP:0001440 abnormal grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:20510925 1557995 Hoxb8 homeobox B8 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:11779477 1557995 Hoxb8 homeobox B8 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:20510925 1557995 Hoxb8 homeobox B8 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:11779477 1557995 Hoxb8 homeobox B8 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:11779477 1557995 Hoxb8 homeobox B8 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:10559485 1557995 Hoxb8 homeobox B8 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10559485 1557995 Hoxb8 homeobox B8 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:20510925 1557995 Hoxb8 homeobox B8 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14623233 1557995 Hoxb8 homeobox B8 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:14623233 1557995 Hoxb8 homeobox B8 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11311170 1557995 Hoxb8 homeobox B8 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:11779477 1557995 Hoxb8 homeobox B8 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11311170 1557995 Hoxb8 homeobox B8 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11311170 1557995 Hoxb8 homeobox B8 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11311170 1557995 Hoxb8 homeobox B8 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:14623233 1557995 Hoxb8 homeobox B8 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:11311170 1557995 Hoxb8 homeobox B8 gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:11311170 1557995 Hoxb8 homeobox B8 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:10559485 1557995 Hoxb8 homeobox B8 gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:20510925 1557995 Hoxb8 homeobox B8 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:11311170 1557995 Hoxb8 homeobox B8 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:10559485 1557995 Hoxb8 homeobox B8 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:14623233 1557995 Hoxb8 homeobox B8 gene MP:0012283 decreased sternebra number IAGP N RGD:5509061 20141003 MGI PMID:14623233 1557997 Glce glucuronyl C5-epimerase gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:12788935 1557997 Glce glucuronyl C5-epimerase gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:12788935 1557997 Glce glucuronyl C5-epimerase gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:12788935 1557997 Glce glucuronyl C5-epimerase gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:12788935 1557997 Glce glucuronyl C5-epimerase gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12788935 1557997 Glce glucuronyl C5-epimerase gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12788935 1557997 Glce glucuronyl C5-epimerase gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:12788935 1557997 Glce glucuronyl C5-epimerase gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:12788935 1557997 Glce glucuronyl C5-epimerase gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:12788935 1557997 Glce glucuronyl C5-epimerase gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:12788935 1557997 Glce glucuronyl C5-epimerase gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:12788935 1557997 Glce glucuronyl C5-epimerase gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:12788935 1557997 Glce glucuronyl C5-epimerase gene MP:0009729 absent tarsus bones IAGP N RGD:5509061 20141003 MGI PMID:12788935 1557997 Glce glucuronyl C5-epimerase gene MP:0010714 iris coloboma IAGP N RGD:5509061 20141003 MGI PMID:12788935 1557997 Glce glucuronyl C5-epimerase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12788935 1557997 Glce glucuronyl C5-epimerase gene MP:0014473 increased pulmonary alveolus wall thickness IAGP N RGD:5509061 20240704 MGI PMID:12788935 1557998 Ppp2r2b protein phosphatase 2, regulatory subunit B, beta gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20221215 MGI 1557998 Ppp2r2b protein phosphatase 2, regulatory subunit B, beta gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 1557998 Ppp2r2b protein phosphatase 2, regulatory subunit B, beta gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1557998 Ppp2r2b protein phosphatase 2, regulatory subunit B, beta gene MP:0001399 hyperactivity IEA N RGD:5509061 20200514 MGI 1557998 Ppp2r2b protein phosphatase 2, regulatory subunit B, beta gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20200310 MGI 1557998 Ppp2r2b protein phosphatase 2, regulatory subunit B, beta gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20200310 MGI 1557998 Ppp2r2b protein phosphatase 2, regulatory subunit B, beta gene MP:0003929 decreased heart rate variability IEA N RGD:5509061 20200514 MGI 1557998 Ppp2r2b protein phosphatase 2, regulatory subunit B, beta gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 1557998 Ppp2r2b protein phosphatase 2, regulatory subunit B, beta gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20200310 MGI 1557998 Ppp2r2b protein phosphatase 2, regulatory subunit B, beta gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20200310 MGI 1557998 Ppp2r2b protein phosphatase 2, regulatory subunit B, beta gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1557999 Rnf216 ring finger protein 216 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20160421 MGI 1557999 Rnf216 ring finger protein 216 gene MP:0001147 small testis IAGP N RGD:5509061 20190926 MGI PMID:30649198 1557999 Rnf216 ring finger protein 216 gene MP:0001147 small testis IAGP N RGD:5509061 20220721 MGI PMID:33724554 1557999 Rnf216 ring finger protein 216 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20220721 MGI PMID:33724554 1557999 Rnf216 ring finger protein 216 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20190926 MGI PMID:30649198 1557999 Rnf216 ring finger protein 216 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20190926 MGI PMID:30649198 1557999 Rnf216 ring finger protein 216 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220721 MGI PMID:33724554 1557999 Rnf216 ring finger protein 216 gene MP:0001925 male infertility IAGP N RGD:5509061 20190926 MGI PMID:30649198 1557999 Rnf216 ring finger protein 216 gene MP:0001925 male infertility IAGP N RGD:5509061 20220721 MGI PMID:33724554 1557999 Rnf216 ring finger protein 216 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20190926 MGI PMID:30649198 1557999 Rnf216 ring finger protein 216 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220721 MGI PMID:33724554 1557999 Rnf216 ring finger protein 216 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220721 MGI PMID:33724554 1557999 Rnf216 ring finger protein 216 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20190926 MGI PMID:30649198 1557999 Rnf216 ring finger protein 216 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220721 MGI PMID:33724554 1557999 Rnf216 ring finger protein 216 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220721 MGI PMID:33724554 1557999 Rnf216 ring finger protein 216 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20190926 MGI PMID:30649198 1557999 Rnf216 ring finger protein 216 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220721 MGI PMID:33724554 1557999 Rnf216 ring finger protein 216 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210520 MGI 1557999 Rnf216 ring finger protein 216 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20220721 MGI PMID:33724554 1557999 Rnf216 ring finger protein 216 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20190926 MGI PMID:30649198 1557999 Rnf216 ring finger protein 216 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220721 MGI PMID:33724554 1557999 Rnf216 ring finger protein 216 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20190926 MGI PMID:30649198 1557999 Rnf216 ring finger protein 216 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20220721 MGI PMID:33724554 1557999 Rnf216 ring finger protein 216 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1557999 Rnf216 ring finger protein 216 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20190926 MGI PMID:30649198 1557999 Rnf216 ring finger protein 216 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220721 MGI PMID:33724554 1558000 Epb41l2 erythrocyte membrane protein band 4.1 like 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:19225127 1558000 Epb41l2 erythrocyte membrane protein band 4.1 like 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19225127 1558000 Epb41l2 erythrocyte membrane protein band 4.1 like 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21482674 1558000 Epb41l2 erythrocyte membrane protein band 4.1 like 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21482674 1558000 Epb41l2 erythrocyte membrane protein band 4.1 like 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21482674 1558000 Epb41l2 erythrocyte membrane protein band 4.1 like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19225127 1558000 Epb41l2 erythrocyte membrane protein band 4.1 like 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21482674 1558000 Epb41l2 erythrocyte membrane protein band 4.1 like 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21482674 1558000 Epb41l2 erythrocyte membrane protein band 4.1 like 2 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21482674 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000075 absent neurocranium IAGP N RGD:5509061 20171102 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000100 abnormal ethmoid bone morphology IAGP N RGD:5509061 20171214 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20171214 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000288 abnormal pericardium morphology IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:12142349 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16873583 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:22449950 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:11802174 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:18647752 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:22449950 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:18647752 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18647752 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:18647752 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18647752 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:18647752 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:12142349 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:12142349 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0002748 abnormal pulmonary valve morphology IAGP N RGD:5509061 20141003 MGI PMID:12142349 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20141003 MGI PMID:18647752 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:18647752 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003044 impaired basement membrane formation IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18647752 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003279 aneurysm IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:22449950 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:12142349 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:12818570 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18647752 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16873583 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004373 bowed humerus IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004419 absent parietal bone IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004669 enlarged vertebral body IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:12142349 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:18647752 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:18647752 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20171214 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12142349 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:22449950 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22449950 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:12514129 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:12142349 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0008160 increased diameter of humerus IAGP N RGD:5509061 20141003 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0008160 increased diameter of humerus IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20160609 MGI PMID:12814946 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:18647752 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:18647752 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:18647752 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0009459 skeletal muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0010426 abnormal heart and great artery attachment IAGP N RGD:5509061 20141003 MGI PMID:12818570 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0010472 abnormal ascending aorta and coronary artery attachment IAGP N RGD:5509061 20141003 MGI PMID:12818570 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0010584 abnormal conotruncus septation IAGP N RGD:5509061 20141003 MGI PMID:12142349 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0010586 absent conotruncal ridges IAGP N RGD:5509061 20141003 MGI PMID:12142349 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0010588 conotruncal ridge hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12142349 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0010732 abnormal node of Ranvier morphology IAGP N RGD:5509061 20141003 MGI PMID:22449950 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0010734 abnormal paranode morphology IAGP N RGD:5509061 20141003 MGI PMID:22449950 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0010738 abnormal internode morphology IAGP N RGD:5509061 20141003 MGI PMID:22449950 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0010742 increased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:22449950 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0011238 abnormal inner ear development IAGP N RGD:5509061 20240912 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0011514 skin hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0012175 flat face IAGP N RGD:5509061 20141003 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0014516 abnormal middle ear development IAGP N RGD:5509061 20240912 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:10579729 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0020390 abnormal radial glial cell endfoot morphology IAGP N RGD:5509061 20161117 MGI PMID:16873583 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20171214 MGI PMID:10545953 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0030788 abnormal femur head morphology IAGP N RGD:5509061 20181011 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0030789 abnormal femur neck morphology IAGP N RGD:5509061 20181011 MGI PMID:17213231 1558001 Hspg2 perlecan (heparan sulfate proteoglycan 2) gene MP:0030793 short femur neck IAGP N RGD:5509061 20181011 MGI PMID:17213231 1558002 Rab19 RAB19, member RAS oncogene family gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210826 MGI 1558002 Rab19 RAB19, member RAS oncogene family gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1558002 Rab19 RAB19, member RAS oncogene family gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20240523 MGI 1558002 Rab19 RAB19, member RAS oncogene family gene MP:0001314 cornea opacity IEA N RGD:5509061 20210826 MGI 1558002 Rab19 RAB19, member RAS oncogene family gene MP:0001469 abnormal contextual conditioning behavior IEA N RGD:5509061 20211021 MGI 1558002 Rab19 RAB19, member RAS oncogene family gene MP:0002833 increased heart weight IEA N RGD:5509061 20160421 MGI 1558002 Rab19 RAB19, member RAS oncogene family gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1558002 Rab19 RAB19, member RAS oncogene family gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20211021 MGI 1558002 Rab19 RAB19, member RAS oncogene family gene MP:0012361 decreased large unstained cell number IEA N RGD:5509061 20160421 MGI 1558003 Zfp280c zinc finger protein 280C gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1558003 Zfp280c zinc finger protein 280C gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20240523 MGI 1558003 Zfp280c zinc finger protein 280C gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20240718 MGI PMID:35605119 1558003 Zfp280c zinc finger protein 280C gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20240718 MGI PMID:35605119 1558003 Zfp280c zinc finger protein 280C gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20240718 MGI PMID:35605119 1558006 Vrk3 vaccinia related kinase 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1558006 Vrk3 vaccinia related kinase 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1558006 Vrk3 vaccinia related kinase 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1558006 Vrk3 vaccinia related kinase 3 gene MP:0001192 scaly skin IEA N RGD:5509061 20210128 MGI 1558006 Vrk3 vaccinia related kinase 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20180208 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20180208 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20180208 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20180208 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20180208 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210128 MGI 1558006 Vrk3 vaccinia related kinase 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1558006 Vrk3 vaccinia related kinase 3 gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20180208 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1558006 Vrk3 vaccinia related kinase 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1558006 Vrk3 vaccinia related kinase 3 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20180208 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20180208 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1558006 Vrk3 vaccinia related kinase 3 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20180208 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20180208 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20180208 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20180208 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20180208 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20180208 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0020510 increased dendritic spine length IAGP N RGD:5509061 20180208 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20180301 MGI PMID:28899869 1558006 Vrk3 vaccinia related kinase 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:28899869 1558007 Rfk riboflavin kinase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1558007 Rfk riboflavin kinase gene MP:0000692 small spleen IEA N RGD:5509061 20230119 MGI 1558007 Rfk riboflavin kinase gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1558007 Rfk riboflavin kinase gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 1558007 Rfk riboflavin kinase gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 1558007 Rfk riboflavin kinase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1558007 Rfk riboflavin kinase gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 1558007 Rfk riboflavin kinase gene MP:0003604 single kidney IEA N RGD:5509061 20230119 MGI 1558007 Rfk riboflavin kinase gene MP:0011077 decreased macrophage nitric oxide production IAGP N RGD:5509061 20141003 MGI PMID:19641494 1558007 Rfk riboflavin kinase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19641494 1558007 Rfk riboflavin kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1558007 Rfk riboflavin kinase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230119 MGI 1558009 Asprv1 aspartic peptidase, retroviral-like 1 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:16837463 1558009 Asprv1 aspartic peptidase, retroviral-like 1 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:16837463 1558012 Fgd1 FYVE, RhoGEF and PH domain containing 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20190502 MGI 1558012 Fgd1 FYVE, RhoGEF and PH domain containing 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220519 MGI 1558012 Fgd1 FYVE, RhoGEF and PH domain containing 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1558012 Fgd1 FYVE, RhoGEF and PH domain containing 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1558012 Fgd1 FYVE, RhoGEF and PH domain containing 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1558012 Fgd1 FYVE, RhoGEF and PH domain containing 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1558013 Ogdh oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1558013 Ogdh oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170504 MGI 1558013 Ogdh oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1558013 Ogdh oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1558013 Ogdh oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150430 MGI 1558013 Ogdh oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20150430 MGI 1558013 Ogdh oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1558013 Ogdh oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558013 Ogdh oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:15846349 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000046 abnormal sulcus ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:15846349 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000397 abnormal guard hair morphology IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000405 abnormal auchene hair morphology IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000467 abnormal esophagus morphology IAGP N RGD:5509061 20141003 MGI PMID:17015430 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000467 abnormal esophagus morphology IAGP N RGD:5509061 20141003 MGI PMID:17522155 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000469 abnormal esophageal squamous epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17522155 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:17015430 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:17522155 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:21982232 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17522155 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:17015430 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:19734891 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19734891 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:19734891 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:19734891 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:19734891 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0000948 nonconvulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21982232 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21982232 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:17140559 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001288 abnormal lens induction IAGP N RGD:5509061 20141003 MGI PMID:17140559 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:16651659 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:17140559 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15882093 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:16651659 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17140559 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19570848 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20230223 MGI PMID:23638914 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:17140559 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20220811 MGI 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:16651659 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:16651659 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001329 retina hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16651659 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:15846349 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17522155 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:12514105 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20141003 MGI PMID:12514105 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20141003 MGI PMID:23029233 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001717 absent ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:12514105 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21982232 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:21982232 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12514105 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17522155 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15846349 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15882093 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:23153495 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15846349 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15882093 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19734891 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21982232 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20150205 MGI PMID:21331042 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15882093 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16651659 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23029233 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002281 abnormal respiratory mucosa goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20011520 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:15846349 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15846349 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002653 abnormal ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002697 abnormal eye size IAGP N RGD:5509061 20141003 MGI PMID:16651659 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16651659 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:15846349 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:15846349 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19570848 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:19734891 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0003276 esophageal atresia IAGP N RGD:5509061 20141003 MGI PMID:17522155 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0003300 gastrointestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:21982232 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:17522155 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19734891 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0003817 abnormal pituitary diverticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:17140559 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20220616 MGI PMID:33964205 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:17140559 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:24094324 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0004317 small vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:15846349 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0004325 absent vestibular hair cells IAGP N RGD:5509061 20141003 MGI PMID:15846349 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0004336 small utricle IAGP N RGD:5509061 20141003 MGI PMID:15846349 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:15846349 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0004416 absent cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0004493 dilated cochlea IAGP N RGD:5509061 20141003 MGI PMID:15846349 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20220616 MGI PMID:33964205 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:21982232 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:18638478 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:19734891 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0005128 decreased adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0005138 decreased prolactin level IAGP N RGD:5509061 20141003 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0005267 abnormal olfactory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15882093 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:12036291 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16651659 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:15846349 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16651659 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0006257 abnormal fungiform papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:17015430 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0006293 absent nasal placodes IAGP N RGD:5509061 20141003 MGI PMID:17140559 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20220616 MGI PMID:33964205 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20011520 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20220811 MGI 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:24209762 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:19734891 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0008329 decreased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:18638478 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:19734891 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0008794 increased lens epithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19570848 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:23029233 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0009453 enhanced contextual conditioning behavior IEA N RGD:5509061 20220519 MGI 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0009533 absent palatine gland IAGP N RGD:5509061 20141003 MGI PMID:17522155 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0009534 absent anterior lingual gland IAGP N RGD:5509061 20141003 MGI PMID:17522155 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20230223 MGI PMID:23638914 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20230223 MGI PMID:23638914 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20230223 MGI PMID:23638914 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19734891 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24094324 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0010371 abnormal epiglottis morphology IAGP N RGD:5509061 20141225 MGI PMID:17522155 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0010863 absent respiratory mucosa goblet cells IAGP N RGD:5509061 20141003 MGI PMID:20011520 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0010897 abnormal bronchiole epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20011520 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0011054 absent respiratory motile cilia IAGP N RGD:5509061 20141003 MGI PMID:20011520 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0011071 absent club cells IAGP N RGD:5509061 20141003 MGI PMID:20011520 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17015430 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17522155 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18638478 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23029233 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12514105 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20170824 MGI PMID:26658019 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15240551 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0011184 absent embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:23029233 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20220616 MGI PMID:33964205 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0013337 abnormal adenohypophysis development IAGP N RGD:5509061 20141204 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0013342 bifurcated Rathke's pouch IAGP N RGD:5509061 20141204 MGI PMID:16932809 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:29743593 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20230223 MGI PMID:23638914 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0030129 tongue inflammation IAGP N RGD:5509061 20171005 MGI PMID:21982232 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0031278 decreased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:29743593 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:0031467 absent palatal taste bud IAGP N RGD:5509061 20230615 MGI PMID:17015430 1558014 Sox2 SRY (sex determining region Y)-box 2 gene MP:3000003 abnormal Ebner's gland morphology IAGP N RGD:5509061 20141225 MGI PMID:17522155 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0001257 increased body length IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0001260 increased body weight IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0001261 obese IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0001433 polyphagia IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558016 Ankrd26 ankyrin repeat domain 26 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20160225 MGI PMID:18162531 1558017 Cd207 CD207 antigen gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20150226 MGI PMID:23118208 1558017 Cd207 CD207 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1558017 Cd207 CD207 antigen gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1558017 Cd207 CD207 antigen gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180830 MGI PMID:24638167 1558017 Cd207 CD207 antigen gene MP:0001861 lung inflammation IAGP N RGD:5509061 20180830 MGI PMID:24638167 1558017 Cd207 CD207 antigen gene MP:0002534 abnormal type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:21998450 1558017 Cd207 CD207 antigen gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:15897263 1558017 Cd207 CD207 antigen gene MP:0008117 abnormal Langerhans cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15601833 1558017 Cd207 CD207 antigen gene MP:0008117 abnormal Langerhans cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15894281 1558017 Cd207 CD207 antigen gene MP:0008118 absent Langerhans cell IAGP N RGD:5509061 20141003 MGI PMID:15894281 1558017 Cd207 CD207 antigen gene MP:0008118 absent Langerhans cell IAGP N RGD:5509061 20141003 MGI PMID:15897263 1558017 Cd207 CD207 antigen gene MP:0008119 decreased Langerhans cell number IAGP N RGD:5509061 20141003 MGI PMID:15894281 1558017 Cd207 CD207 antigen gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20180830 MGI PMID:24638167 1558017 Cd207 CD207 antigen gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:18591406 1558017 Cd207 CD207 antigen gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:21998450 1558017 Cd207 CD207 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1558017 Cd207 CD207 antigen gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1558017 Cd207 CD207 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1558017 Cd207 CD207 antigen gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:18591406 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16311594 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0011261 abnormal limb mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:20920500 1558019 Ofd1 OFD1, centriole and centriolar satellite protein gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20211021 MGI PMID:16311594 1558020 Npsr1 neuropeptide S receptor 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1558020 Npsr1 neuropeptide S receptor 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16829631 1558020 Npsr1 neuropeptide S receptor 1 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20220623 MGI PMID:31619542 1558020 Npsr1 neuropeptide S receptor 1 gene MP:0010936 decreased airway resistance IAGP N RGD:5509061 20141003 MGI PMID:16829631 1558020 Npsr1 neuropeptide S receptor 1 gene MP:0012288 abnormal paradoxical sleep pattern IAGP N RGD:5509061 20220623 MGI PMID:31619542 1558020 Npsr1 neuropeptide S receptor 1 gene MP:0012289 abnormal non-rapid eye movement sleep pattern IAGP N RGD:5509061 20220623 MGI PMID:31619542 1558020 Npsr1 neuropeptide S receptor 1 gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20220623 MGI PMID:31619542 1558020 Npsr1 neuropeptide S receptor 1 gene MP:0020478 abnormal circadian sleep/wake cycle IAGP N RGD:5509061 20220623 MGI PMID:31619542 1558021 Jaml junction adhesion molecule like gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20210304 MGI PMID:33186558 1558021 Jaml junction adhesion molecule like gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20210304 MGI PMID:33186558 1558021 Jaml junction adhesion molecule like gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20210304 MGI PMID:33186558 1558021 Jaml junction adhesion molecule like gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20210304 MGI PMID:33186558 1558021 Jaml junction adhesion molecule like gene MP:0011282 increased podocyte apoptosis IAGP N RGD:5509061 20210304 MGI PMID:33186558 1558021 Jaml junction adhesion molecule like gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20210304 MGI PMID:33186558 1558021 Jaml junction adhesion molecule like gene MP:0011561 renal glomerulus lipidosis IAGP N RGD:5509061 20210304 MGI PMID:33186558 1558021 Jaml junction adhesion molecule like gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20210304 MGI PMID:33186558 1558021 Jaml junction adhesion molecule like gene MP:0020153 abnormal urine albumin level IAGP N RGD:5509061 20210304 MGI PMID:33186558 1558022 Trappc2 trafficking protein particle complex 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20210520 MGI 1558022 Trappc2 trafficking protein particle complex 2 gene MP:0005575 increased pulmonary ventilation IEA N RGD:5509061 20210128 MGI 1558022 Trappc2 trafficking protein particle complex 2 gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20210128 MGI 1558022 Trappc2 trafficking protein particle complex 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20170105 MGI 1558022 Trappc2 trafficking protein particle complex 2 gene MP:0012125 decreased bronchoconstrictive response IEA N RGD:5509061 20210128 MGI 1558023 Kbtbd11 kelch repeat and BTB (POZ) domain containing 11 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200514 MGI 1558023 Kbtbd11 kelch repeat and BTB (POZ) domain containing 11 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200514 MGI 1558023 Kbtbd11 kelch repeat and BTB (POZ) domain containing 11 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20200514 MGI 1558023 Kbtbd11 kelch repeat and BTB (POZ) domain containing 11 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200514 MGI 1558023 Kbtbd11 kelch repeat and BTB (POZ) domain containing 11 gene MP:0001147 small testis IEA N RGD:5509061 20200514 MGI 1558023 Kbtbd11 kelch repeat and BTB (POZ) domain containing 11 gene MP:0001262 decreased body weight IEA N RGD:5509061 20240523 MGI 1558023 Kbtbd11 kelch repeat and BTB (POZ) domain containing 11 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20200514 MGI 1558023 Kbtbd11 kelch repeat and BTB (POZ) domain containing 11 gene MP:0009709 hydrometra IEA N RGD:5509061 20200514 MGI 1558023 Kbtbd11 kelch repeat and BTB (POZ) domain containing 11 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1558024 Atp11c ATPase, class VI, type 11C gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1558024 Atp11c ATPase, class VI, type 11C gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1558024 Atp11c ATPase, class VI, type 11C gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1558024 Atp11c ATPase, class VI, type 11C gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1558024 Atp11c ATPase, class VI, type 11C gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 1558024 Atp11c ATPase, class VI, type 11C gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1558024 Atp11c ATPase, class VI, type 11C gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1558024 Atp11c ATPase, class VI, type 11C gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1558024 Atp11c ATPase, class VI, type 11C gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20220811 MGI 1558024 Atp11c ATPase, class VI, type 11C gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008170 decreased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008175 absent follicular B cells IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423173 1558024 Atp11c ATPase, class VI, type 11C gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558024 Atp11c ATPase, class VI, type 11C gene MP:0010228 decreased transitional stage T3 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21423172 1558027 Hmx2 H6 homeobox 2 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11748138 1558027 Hmx2 H6 homeobox 2 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:11748138 1558027 Hmx2 H6 homeobox 2 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:11748138 1558027 Hmx2 H6 homeobox 2 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0000041 absent endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11748138 1558027 Hmx2 H6 homeobox 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11748138 1558027 Hmx2 H6 homeobox 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0001752 abnormal hypothalamus secretion IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1558027 Hmx2 H6 homeobox 2 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0002859 abnormal inner ear canal fusion IAGP N RGD:5509061 20141003 MGI PMID:11748138 1558027 Hmx2 H6 homeobox 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20170105 MGI 1558027 Hmx2 H6 homeobox 2 gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 1558027 Hmx2 H6 homeobox 2 gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20141003 MGI PMID:11748138 1558027 Hmx2 H6 homeobox 2 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:11748138 1558027 Hmx2 H6 homeobox 2 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0004328 decreased vestibular hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0004329 vestibular saccular degeneration IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0004332 utricular degeneration IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1558027 Hmx2 H6 homeobox 2 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:11748138 1558027 Hmx2 H6 homeobox 2 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20170105 MGI 1558027 Hmx2 H6 homeobox 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20181227 MGI 1558027 Hmx2 H6 homeobox 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15363417 1558027 Hmx2 H6 homeobox 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1558030 Opn3 opsin 3 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20201015 MGI PMID:31968245 1558030 Opn3 opsin 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1558030 Opn3 opsin 3 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20231207 MGI 1558030 Opn3 opsin 3 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20201015 MGI PMID:31968245 1558030 Opn3 opsin 3 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20201015 MGI PMID:31968245 1558030 Opn3 opsin 3 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20201015 MGI PMID:31968245 1558030 Opn3 opsin 3 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20201015 MGI PMID:31968245 1558030 Opn3 opsin 3 gene MP:0009132 abnormal white fat cell size IAGP N RGD:5509061 20201015 MGI PMID:31968245 1558030 Opn3 opsin 3 gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20201015 MGI PMID:31968245 1558030 Opn3 opsin 3 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20201015 MGI PMID:31968245 1558030 Opn3 opsin 3 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20201015 MGI PMID:31968245 1558030 Opn3 opsin 3 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20201015 MGI PMID:31968245 1558030 Opn3 opsin 3 gene MP:0011973 abnormal circulating glycerol level IAGP N RGD:5509061 20201015 MGI PMID:31968245 1558030 Opn3 opsin 3 gene MP:0020325 abnormal beige fat cell morphology IAGP N RGD:5509061 20201015 MGI PMID:31968245 1558032 Hccs holocytochrome c synthetase gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:12444108 1558032 Hccs holocytochrome c synthetase gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:12444108 1558032 Hccs holocytochrome c synthetase gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12444108 1558032 Hccs holocytochrome c synthetase gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12444108 1558032 Hccs holocytochrome c synthetase gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0010520 sinoatrial block IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0010636 bundle branch block IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12444108 1558032 Hccs holocytochrome c synthetase gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20240321 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0014072 decreased cardiac muscle glycogen level IAGP N RGD:5509061 20191226 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0031607 abnormal fetal cardiomyocyte mitochondrial morphology IAGP N RGD:5509061 20240321 MGI PMID:18854137 1558032 Hccs holocytochrome c synthetase gene MP:0031608 decreased fetal cardiomyocyte size IAGP N RGD:5509061 20240321 MGI PMID:18854137 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0000160 kyphosis IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0000751 myopathy IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0001263 weight loss IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0001513 limb grasping IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0002083 premature death IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0002083 premature death IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20180315 MGI PMID:29112723 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20211021 MGI 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20180315 MGI PMID:29112723 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0011637 abnormal mitochondrial matrix morphology IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0014342 abnormal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240215 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0014390 decreased myocardial fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:35700042 1558033 Chchd10 coiled-coil-helix-coiled-coil-helix domain containing 10 gene MP:0020851 abnormal vacuole morphology IAGP N RGD:5509061 20190411 MGI PMID:30877432 1558034 Rint1 RAD50 interactor 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1558034 Rint1 RAD50 interactor 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20220811 MGI 1558034 Rint1 RAD50 interactor 1 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0003570 increased uterus leiomyoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1558034 Rint1 RAD50 interactor 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1558034 Rint1 RAD50 interactor 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20201022 MGI 1558034 Rint1 RAD50 interactor 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1558034 Rint1 RAD50 interactor 1 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0010309 increased mesothelioma incidence IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558034 Rint1 RAD50 interactor 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1558034 Rint1 RAD50 interactor 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1558034 Rint1 RAD50 interactor 1 gene MP:0013488 increased keratoacanthoma incidence IAGP N RGD:5509061 20150212 MGI PMID:17470549 1558034 Rint1 RAD50 interactor 1 gene MP:0013751 increased cystadenoma incidence IAGP N RGD:5509061 20150416 MGI PMID:17470549 1558038 Sec14l1 SEC14-like lipid binding 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1558038 Sec14l1 SEC14-like lipid binding 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1558038 Sec14l1 SEC14-like lipid binding 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1558038 Sec14l1 SEC14-like lipid binding 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1558040 Cd96 CD96 antigen gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1558040 Cd96 CD96 antigen gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20191219 MGI PMID:24658051 1558040 Cd96 CD96 antigen gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20190425 MGI PMID:24658051 1558040 Cd96 CD96 antigen gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20191219 MGI PMID:24658051 1558040 Cd96 CD96 antigen gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20191219 MGI PMID:24658051 1558040 Cd96 CD96 antigen gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20190425 MGI PMID:24658051 1558041 Dab1 disabled 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:21315259 1558041 Dab1 disabled 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:8875886 1558041 Dab1 disabled 1 gene MP:0000746 weakness IEA N RGD:5509061 20141003 MGI 1558041 Dab1 disabled 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10959835 1558041 Dab1 disabled 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15249135 1558041 Dab1 disabled 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18981215 1558041 Dab1 disabled 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:8875886 1558041 Dab1 disabled 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:18981215 1558041 Dab1 disabled 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:8875886 1558041 Dab1 disabled 1 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:10959835 1558041 Dab1 disabled 1 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:11830577 1558041 Dab1 disabled 1 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15249135 1558041 Dab1 disabled 1 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:18981215 1558041 Dab1 disabled 1 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21315259 1558041 Dab1 disabled 1 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:24210661 1558041 Dab1 disabled 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15249135 1558041 Dab1 disabled 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:18981215 1558041 Dab1 disabled 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:8875886 1558041 Dab1 disabled 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:10959835 1558041 Dab1 disabled 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:11830577 1558041 Dab1 disabled 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:8875886 1558041 Dab1 disabled 1 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17182786 1558041 Dab1 disabled 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 1558041 Dab1 disabled 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:18981215 1558041 Dab1 disabled 1 gene MP:0000851 cerebellum hypoplasia IEA N RGD:5509061 20111116 MGI 1558041 Dab1 disabled 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:10959835 1558041 Dab1 disabled 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:18029196 1558041 Dab1 disabled 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:18981215 1558041 Dab1 disabled 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:8875886 1558041 Dab1 disabled 1 gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:10959835 1558041 Dab1 disabled 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:24210661 1558041 Dab1 disabled 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:18029196 1558041 Dab1 disabled 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:8875886 1558041 Dab1 disabled 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:10959835 1558041 Dab1 disabled 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:18029196 1558041 Dab1 disabled 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:8875886 1558041 Dab1 disabled 1 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:18029196 1558041 Dab1 disabled 1 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:18981215 1558041 Dab1 disabled 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10959835 1558041 Dab1 disabled 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:18981215 1558041 Dab1 disabled 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:21315259 1558041 Dab1 disabled 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8875886 1558041 Dab1 disabled 1 gene MP:0001391 abnormal tail movements IAGP N RGD:5509061 20141003 MGI PMID:10959835 1558041 Dab1 disabled 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10959835 1558041 Dab1 disabled 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18029196 1558041 Dab1 disabled 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21315259 1558041 Dab1 disabled 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:8875886 1558041 Dab1 disabled 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:8875886 1558041 Dab1 disabled 1 gene MP:0001523 impaired righting response IEA N RGD:5509061 20111116 MGI 1558041 Dab1 disabled 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:10959835 1558041 Dab1 disabled 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8875886 1558041 Dab1 disabled 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8875886 1558041 Dab1 disabled 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10959835 1558041 Dab1 disabled 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10959835 1558041 Dab1 disabled 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:18029196 1558041 Dab1 disabled 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10959835 1558041 Dab1 disabled 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15249135 1558041 Dab1 disabled 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21315259 1558041 Dab1 disabled 1 gene MP:0002397 abnormal bone marrow morphology IEA N RGD:5509061 20111116 MGI 1558041 Dab1 disabled 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:18029196 1558041 Dab1 disabled 1 gene MP:0003644 thymus atrophy IEA N RGD:5509061 20111116 MGI 1558041 Dab1 disabled 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11580894 1558041 Dab1 disabled 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11580894 1558041 Dab1 disabled 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11580894 1558041 Dab1 disabled 1 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 1558041 Dab1 disabled 1 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 1558041 Dab1 disabled 1 gene MP:0005150 cachexia IEA N RGD:5509061 20111116 MGI 1558041 Dab1 disabled 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:11830577 1558041 Dab1 disabled 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:21315259 1558041 Dab1 disabled 1 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11580894 1558041 Dab1 disabled 1 gene MP:0008265 abnormal hippocampus CA2 region morphology IAGP N RGD:5509061 20141003 MGI PMID:10959835 1558041 Dab1 disabled 1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:11830577 1558041 Dab1 disabled 1 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:24210661 1558041 Dab1 disabled 1 gene MP:0008440 abnormal subplate morphology IAGP N RGD:5509061 20141003 MGI PMID:18981215 1558041 Dab1 disabled 1 gene MP:0008443 absent subplate IAGP N RGD:5509061 20141003 MGI PMID:21315259 1558041 Dab1 disabled 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21315259 1558041 Dab1 disabled 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:8875886 1558041 Dab1 disabled 1 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8875886 1558041 Dab1 disabled 1 gene MP:0009949 abnormal olfactory bulb granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 1558041 Dab1 disabled 1 gene MP:0009956 abnormal cerebellar layer morphology IEA N RGD:5509061 20141003 MGI 1558041 Dab1 disabled 1 gene MP:0011083 lethality at weaning, complete penetrance IEA N RGD:5509061 20141003 MGI 1558041 Dab1 disabled 1 gene MP:0011085 postnatal lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 1558041 Dab1 disabled 1 gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1558041 Dab1 disabled 1 gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1558041 Dab1 disabled 1 gene MP:0013138 thin body IEA N RGD:5509061 20141003 MGI 1558041 Dab1 disabled 1 gene MP:0030956 abnormal neuronal precursor cell migration IAGP N RGD:5509061 20190725 MGI PMID:17494763 1558042 Efhb EF hand domain family, member B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1558042 Efhb EF hand domain family, member B gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1558042 Efhb EF hand domain family, member B gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1558043 Lrch1 leucine-rich repeats and calponin homology (CH) domain containing 1 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180329 MGI PMID:28028151 1558043 Lrch1 leucine-rich repeats and calponin homology (CH) domain containing 1 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20180329 MGI PMID:28028151 1558044 Slc6a14 solute carrier family 6 (neurotransmitter transporter), member 14 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20161201 MGI PMID:26173258 1558044 Slc6a14 solute carrier family 6 (neurotransmitter transporter), member 14 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20161201 MGI PMID:26173258 1558044 Slc6a14 solute carrier family 6 (neurotransmitter transporter), member 14 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210805 MGI 1558044 Slc6a14 solute carrier family 6 (neurotransmitter transporter), member 14 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20161201 MGI PMID:26173258 1558044 Slc6a14 solute carrier family 6 (neurotransmitter transporter), member 14 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210805 MGI 1558044 Slc6a14 solute carrier family 6 (neurotransmitter transporter), member 14 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20161201 MGI PMID:26173258 1558044 Slc6a14 solute carrier family 6 (neurotransmitter transporter), member 14 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210805 MGI 1558044 Slc6a14 solute carrier family 6 (neurotransmitter transporter), member 14 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20221215 MGI 1558044 Slc6a14 solute carrier family 6 (neurotransmitter transporter), member 14 gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20161201 MGI PMID:26173258 1558044 Slc6a14 solute carrier family 6 (neurotransmitter transporter), member 14 gene MP:0008639 decreased circulating interleukin-1 alpha level IAGP N RGD:5509061 20161201 MGI PMID:26173258 1558044 Slc6a14 solute carrier family 6 (neurotransmitter transporter), member 14 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20161201 MGI PMID:26173258 1558044 Slc6a14 solute carrier family 6 (neurotransmitter transporter), member 14 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20161201 MGI PMID:26173258 1558044 Slc6a14 solute carrier family 6 (neurotransmitter transporter), member 14 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20161201 MGI PMID:26173258 1558044 Slc6a14 solute carrier family 6 (neurotransmitter transporter), member 14 gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20161201 MGI PMID:26173258 1558045 Slamf6 SLAM family member 6 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1558045 Slamf6 SLAM family member 6 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15879084 1558045 Slamf6 SLAM family member 6 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:15879084 1558045 Slamf6 SLAM family member 6 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15879084 1558045 Slamf6 SLAM family member 6 gene MP:0005074 impaired granulocyte bactericidal activity IAGP N RGD:5509061 20141003 MGI PMID:15879084 1558045 Slamf6 SLAM family member 6 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:15879084 1558045 Slamf6 SLAM family member 6 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15879084 1558045 Slamf6 SLAM family member 6 gene MP:0008632 increased circulating interleukin-16 level IAGP N RGD:5509061 20141003 MGI PMID:15879084 1558045 Slamf6 SLAM family member 6 gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:15879084 1558045 Slamf6 SLAM family member 6 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15879084 1558045 Slamf6 SLAM family member 6 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15879084 1558047 Agbl3 ATP/GTP binding protein-like 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150122 MGI PMID:25103237 1558048 Sema4c sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:21122816 1558048 Sema4c sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21122816 1558048 Sema4c sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21122816 1558048 Sema4c sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:21122816 1558048 Sema4c sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C gene MP:0009964 abnormal cerebellum lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:21122816 1558048 Sema4c sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20141003 MGI PMID:21122816 1558048 Sema4c sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21122816 1558050 Uqcrq ubiquinol-cytochrome c reductase, complex III subunit VII gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 1558050 Uqcrq ubiquinol-cytochrome c reductase, complex III subunit VII gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558050 Uqcrq ubiquinol-cytochrome c reductase, complex III subunit VII gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1558051 Galntl5 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:24398516 1558051 Galntl5 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:24398516 1558051 Galntl5 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:24398516 1558051 Galntl5 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:24398516 1558051 Galntl5 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:24398516 1558051 Galntl5 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:24398516 1558051 Galntl5 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20200402 MGI 1558051 Galntl5 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase-like 5 gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20220811 MGI 1558053 Morc4 microrchidia 4 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1558053 Morc4 microrchidia 4 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210128 MGI 1558053 Morc4 microrchidia 4 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1558053 Morc4 microrchidia 4 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1558053 Morc4 microrchidia 4 gene MP:0003900 shortened QT interval IEA N RGD:5509061 20230601 MGI 1558053 Morc4 microrchidia 4 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1558054 Acot3 acyl-CoA thioesterase 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20201022 MGI 1558054 Acot3 acyl-CoA thioesterase 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1558054 Acot3 acyl-CoA thioesterase 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20201022 MGI 1558054 Acot3 acyl-CoA thioesterase 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1558054 Acot3 acyl-CoA thioesterase 3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210826 MGI 1558054 Acot3 acyl-CoA thioesterase 3 gene MP:0020422 decreased freezing behavior IEA N RGD:5509061 20231207 MGI 1558057 Parn poly(A)-specific ribonuclease (deadenylation nuclease) gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200430 MGI PMID:31273937 1558059 Hmces 5-hydroxymethylcytosine (hmC) binding, ES cell specific gene MP:0001935 decreased litter size IAGP N RGD:5509061 20180524 MGI PMID:29020633 1558059 Hmces 5-hydroxymethylcytosine (hmC) binding, ES cell specific gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180524 MGI PMID:29020633 1558059 Hmces 5-hydroxymethylcytosine (hmC) binding, ES cell specific gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20180524 MGI PMID:29020633 1558059 Hmces 5-hydroxymethylcytosine (hmC) binding, ES cell specific gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20180524 MGI PMID:29020633 1558059 Hmces 5-hydroxymethylcytosine (hmC) binding, ES cell specific gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20180524 MGI PMID:29020633 1558059 Hmces 5-hydroxymethylcytosine (hmC) binding, ES cell specific gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20180524 MGI PMID:29020633 1558060 Hoxa11 homeobox A11 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:7902826 1558060 Hoxa11 homeobox A11 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0000524 decreased renal tubule number IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:11493536 1558060 Hoxa11 homeobox A11 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:12050119 1558060 Hoxa11 homeobox A11 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:7902826 1558060 Hoxa11 homeobox A11 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:9250683 1558060 Hoxa11 homeobox A11 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:9521905 1558060 Hoxa11 homeobox A11 gene MP:0000553 absent radius IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9250683 1558060 Hoxa11 homeobox A11 gene MP:0000555 absent carpal bone IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:7902826 1558060 Hoxa11 homeobox A11 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:9521905 1558060 Hoxa11 homeobox A11 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:7789268 1558060 Hoxa11 homeobox A11 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:7789268 1558060 Hoxa11 homeobox A11 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12217321 1558060 Hoxa11 homeobox A11 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:7789268 1558060 Hoxa11 homeobox A11 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12050119 1558060 Hoxa11 homeobox A11 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12217321 1558060 Hoxa11 homeobox A11 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18942146 1558060 Hoxa11 homeobox A11 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:7789268 1558060 Hoxa11 homeobox A11 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12050119 1558060 Hoxa11 homeobox A11 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12217321 1558060 Hoxa11 homeobox A11 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18942146 1558060 Hoxa11 homeobox A11 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:7789268 1558060 Hoxa11 homeobox A11 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:7789268 1558060 Hoxa11 homeobox A11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11493536 1558060 Hoxa11 homeobox A11 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12050119 1558060 Hoxa11 homeobox A11 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:7902826 1558060 Hoxa11 homeobox A11 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:9521905 1558060 Hoxa11 homeobox A11 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:7789268 1558060 Hoxa11 homeobox A11 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:7789268 1558060 Hoxa11 homeobox A11 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9250683 1558060 Hoxa11 homeobox A11 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1558060 Hoxa11 homeobox A11 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:7902826 1558060 Hoxa11 homeobox A11 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12050119 1558060 Hoxa11 homeobox A11 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0003600 ectopic kidney IAGP N RGD:5509061 20141003 MGI PMID:12050119 1558060 Hoxa11 homeobox A11 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:12050119 1558060 Hoxa11 homeobox A11 gene MP:0003613 abnormal kidney medulla development IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0003626 kidney medulla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:11493536 1558060 Hoxa11 homeobox A11 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:12050119 1558060 Hoxa11 homeobox A11 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1558060 Hoxa11 homeobox A11 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1558060 Hoxa11 homeobox A11 gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:7789268 1558060 Hoxa11 homeobox A11 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:12217321 1558060 Hoxa11 homeobox A11 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:12217321 1558060 Hoxa11 homeobox A11 gene MP:0004360 absent ulna IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1558060 Hoxa11 homeobox A11 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12869760 1558060 Hoxa11 homeobox A11 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1558060 Hoxa11 homeobox A11 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7902826 1558060 Hoxa11 homeobox A11 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0004649 decreased sacral vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0004650 increased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:12217321 1558060 Hoxa11 homeobox A11 gene MP:0004650 increased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0004650 increased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:7902826 1558060 Hoxa11 homeobox A11 gene MP:0004650 increased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:9250683 1558060 Hoxa11 homeobox A11 gene MP:0004656 absent sacral vertebrae IAGP N RGD:5509061 20141003 MGI PMID:12869760 1558060 Hoxa11 homeobox A11 gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:11493536 1558060 Hoxa11 homeobox A11 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:7902826 1558060 Hoxa11 homeobox A11 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:9250683 1558060 Hoxa11 homeobox A11 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:9521905 1558060 Hoxa11 homeobox A11 gene MP:0005109 abnormal talus morphology IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:7789268 1558060 Hoxa11 homeobox A11 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0008159 increased diameter of fibula IAGP N RGD:5509061 20141003 MGI PMID:11493536 1558060 Hoxa11 homeobox A11 gene MP:0008159 increased diameter of fibula IAGP N RGD:5509061 20141003 MGI PMID:9521905 1558060 Hoxa11 homeobox A11 gene MP:0008161 increased diameter of radius IAGP N RGD:5509061 20141003 MGI PMID:12217321 1558060 Hoxa11 homeobox A11 gene MP:0008161 increased diameter of radius IAGP N RGD:5509061 20141003 MGI PMID:9521905 1558060 Hoxa11 homeobox A11 gene MP:0008162 increased diameter of tibia IAGP N RGD:5509061 20141003 MGI PMID:9521905 1558060 Hoxa11 homeobox A11 gene MP:0008163 increased diameter of ulna IAGP N RGD:5509061 20141003 MGI PMID:12217321 1558060 Hoxa11 homeobox A11 gene MP:0008163 increased diameter of ulna IAGP N RGD:5509061 20141003 MGI PMID:9521905 1558060 Hoxa11 homeobox A11 gene MP:0008258 thin endometrium IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:12217321 1558060 Hoxa11 homeobox A11 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:7902826 1558060 Hoxa11 homeobox A11 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:9250683 1558060 Hoxa11 homeobox A11 gene MP:0009096 decreased endometrial gland number IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0009097 absent endometrial glands IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0009214 vas deferens hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7789268 1558060 Hoxa11 homeobox A11 gene MP:0009728 abnormal calcaneum morphology IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:12050119 1558060 Hoxa11 homeobox A11 gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:12050119 1558060 Hoxa11 homeobox A11 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:11493536 1558060 Hoxa11 homeobox A11 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11688568 1558060 Hoxa11 homeobox A11 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0011366 absent metanephros IAGP N RGD:5509061 20141003 MGI PMID:12050119 1558060 Hoxa11 homeobox A11 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12050119 1558060 Hoxa11 homeobox A11 gene MP:0011565 kidney papillary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7596412 1558060 Hoxa11 homeobox A11 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:7789268 1558060 Hoxa11 homeobox A11 gene MP:0014320 abnormal autopod rotation IAGP N RGD:5509061 20240404 MGI PMID:7596412 1558061 Sez6l seizure related 6 homolog like gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20201022 MGI 1558061 Sez6l seizure related 6 homolog like gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20160421 MGI 1558061 Sez6l seizure related 6 homolog like gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16814779 1558061 Sez6l seizure related 6 homolog like gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 1558061 Sez6l seizure related 6 homolog like gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1558061 Sez6l seizure related 6 homolog like gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20201022 MGI 1558061 Sez6l seizure related 6 homolog like gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16814779 1558061 Sez6l seizure related 6 homolog like gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1558061 Sez6l seizure related 6 homolog like gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20141003 MGI PMID:16814779 1558061 Sez6l seizure related 6 homolog like gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160421 MGI 1558061 Sez6l seizure related 6 homolog like gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20170105 MGI 1558061 Sez6l seizure related 6 homolog like gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20210128 MGI 1558061 Sez6l seizure related 6 homolog like gene MP:0011268 biphasic excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:16814779 1558061 Sez6l seizure related 6 homolog like gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:16814779 1558061 Sez6l seizure related 6 homolog like gene MP:0011272 short excitatory postsynaptic current rise time IAGP N RGD:5509061 20141003 MGI PMID:16814779 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:19965762 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:10662643 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:24265785 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9367153 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:10662643 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:24265785 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:9367153 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10662643 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19965762 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24265785 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9367153 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:19965762 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000874 irregular external granule cell layer thickness IAGP N RGD:5509061 20141003 MGI PMID:19965762 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:10662643 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:9367153 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:17878293 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:24265785 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:24265785 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10662643 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9367153 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10662643 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:9367153 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:24265785 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19965762 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:24717433 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12441305 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0002623 abnormal vestibular hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12441305 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:24717433 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0003247 abnormal glutaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19439493 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0004325 absent vestibular hair cells IAGP N RGD:5509061 20141003 MGI PMID:10364557 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12441305 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:24265785 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:24265785 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:10364557 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:12441305 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:24265785 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:24265785 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:24265785 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17570220 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:19965762 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:19914183 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17878293 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:16202705 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:24265785 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17570220 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10662643 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17570220 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19914183 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20533400 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9367153 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:24265785 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0012490 abnormal cochlear VIII nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19439493 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:19965762 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20161117 MGI PMID:19965762 1558062 Atoh1 atonal bHLH transcription factor 1 gene MP:0031319 impaired intestine regeneration IAGP N RGD:5509061 20211125 MGI PMID:17570220 1558064 Exph5 exophilin 5 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1558064 Exph5 exophilin 5 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1558064 Exph5 exophilin 5 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20211202 MGI PMID:32240120 1558064 Exph5 exophilin 5 gene MP:0002944 increased lactate dehydrogenase level IAGP N RGD:5509061 20211202 MGI PMID:32240120 1558064 Exph5 exophilin 5 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20211202 MGI PMID:32240120 1558064 Exph5 exophilin 5 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1558064 Exph5 exophilin 5 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20211202 MGI PMID:32240120 1558064 Exph5 exophilin 5 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1558064 Exph5 exophilin 5 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20211202 MGI PMID:32240120 1558064 Exph5 exophilin 5 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20210128 MGI 1558064 Exph5 exophilin 5 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20211202 MGI PMID:32240120 1558064 Exph5 exophilin 5 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20211202 MGI PMID:32240120 1558064 Exph5 exophilin 5 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20211202 MGI PMID:32240120 1558064 Exph5 exophilin 5 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20151203 MGI 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20151203 MGI 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0001512 trunk curl IEA N RGD:5509061 20201022 MGI 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0001625 cardiac hypertrophy IEA N RGD:5509061 20141003 MGI 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0002767 situs ambiguus IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0006063 abnormal inferior vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20201022 MGI 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0010476 coronary fistula IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0010854 lung situs inversus IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0011250 abdominal situs ambiguus IEA N RGD:5509061 20151203 MGI 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0011252 situs inversus totalis IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0011649 immotile respiratory cilia IEA N RGD:5509061 20141003 MGI 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0011665 d-loop transposition of the great arteries IEA N RGD:5509061 20151203 MGI 1558065 Dnaaf4 dynein axonemal assembly factor 4 gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23872636 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20160128 MGI PMID:21515572 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20201022 MGI 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20210128 MGI 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20160128 MGI PMID:21515572 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20654612 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20978075 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21262862 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000919 cranioschisis IAGP N RGD:5509061 20141003 MGI PMID:20654612 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:20978075 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:21262862 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20210128 MGI 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20210128 MGI 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20654612 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:21262862 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:20654612 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:20978075 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:20654612 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:20978075 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:21262862 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20201022 MGI 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0003257 abnormal abdominal wall morphology IEA N RGD:5509061 20210128 MGI 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0003385 abnormal body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20201022 MGI 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:21262862 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20201022 MGI 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20978075 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0004391 abnormal respiratory conducting tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0004604 abnormal vertebral pedicle morphology IAGP N RGD:5509061 20240404 MGI PMID:20654612 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0004838 abnormal neural fold elevation formation IAGP N RGD:5509061 20141003 MGI PMID:20654612 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0004838 abnormal neural fold elevation formation IAGP N RGD:5509061 20141003 MGI PMID:20978075 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20200514 MGI 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:20654612 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:20978075 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:21262862 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0010976 small lung lobe IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20654612 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20978075 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21262862 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20210128 MGI 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0012260 encephalomeningocele IAGP N RGD:5509061 20160128 MGI PMID:21515572 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0012544 abnormal caudal neuropore morphology IAGP N RGD:5509061 20141003 MGI PMID:21262862 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0012686 everted embryonic neuroepithelium IAGP N RGD:5509061 20141003 MGI PMID:20978075 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0012707 incomplete caudal neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:20654612 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0012707 incomplete caudal neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:20978075 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20170928 MGI PMID:21377456 1558066 Grhl2 grainyhead like transcription factor 2 gene MP:0030579 thoracoabdominoschisis IAGP N RGD:5509061 20180607 MGI PMID:21377456 1558067 Lrriq1 leucine-rich repeats and IQ motif containing 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20240905 MGI PMID:36129630 1558067 Lrriq1 leucine-rich repeats and IQ motif containing 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240905 MGI PMID:36129630 1558067 Lrriq1 leucine-rich repeats and IQ motif containing 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20240905 MGI PMID:36129630 1558068 Unc5cl unc-5 family C-terminal like gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 1558068 Unc5cl unc-5 family C-terminal like gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1558068 Unc5cl unc-5 family C-terminal like gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1558068 Unc5cl unc-5 family C-terminal like gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1558068 Unc5cl unc-5 family C-terminal like gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1558068 Unc5cl unc-5 family C-terminal like gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1558068 Unc5cl unc-5 family C-terminal like gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210520 MGI 1558069 Hspa1a heat shock protein 1A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11713291 1558069 Hspa1a heat shock protein 1A gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:11713291 1558070 Siva1 SIVA1, apoptosis-inducing factor gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1558070 Siva1 SIVA1, apoptosis-inducing factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150910 MGI PMID:25813352 1558070 Siva1 SIVA1, apoptosis-inducing factor gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20150910 MGI PMID:25813352 1558070 Siva1 SIVA1, apoptosis-inducing factor gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20150910 MGI PMID:25813352 1558070 Siva1 SIVA1, apoptosis-inducing factor gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20150910 MGI PMID:25813352 1558070 Siva1 SIVA1, apoptosis-inducing factor gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1558070 Siva1 SIVA1, apoptosis-inducing factor gene MP:0020190 abnormal lung adenoma incidence IAGP N RGD:5509061 20150910 MGI PMID:25813352 1558071 Mbnl3 muscleblind like splicing factor 3 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:23660517 1558071 Mbnl3 muscleblind like splicing factor 3 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:23660517 1558071 Mbnl3 muscleblind like splicing factor 3 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23660517 1558071 Mbnl3 muscleblind like splicing factor 3 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:23660517 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15051870 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:15051870 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:15051870 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15051870 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12640454 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:15051870 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12640454 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12640454 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:15051870 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12640454 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:19759306 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15051870 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20141003 MGI PMID:19759306 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:12640454 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12640454 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0004560 abnormal chorionic plate morphology IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:19759306 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19759306 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0009656 delayed chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0009658 increased placenta apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0009683 abnormal lateral corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:19759306 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12640454 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12640454 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14749382 1558075 Pnpla6 patatin-like phospholipase domain containing 6 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:12640454 1558077 Ankrd28 ankyrin repeat domain 28 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1558077 Ankrd28 ankyrin repeat domain 28 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1558077 Ankrd28 ankyrin repeat domain 28 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20240523 MGI 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20170302 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20170302 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20170302 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20170302 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20170302 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170302 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20170302 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170302 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20170302 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19509342 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19509342 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19509342 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20170302 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20170302 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20170302 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19509342 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20170302 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0010008 abnormal Purkinje cell migration IAGP N RGD:5509061 20170302 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19509342 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20170302 MGI PMID:26035387 1558078 Sun2 Sad1 and UNC84 domain containing 2 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 1558079 Htatsf1 HIV TAT specific factor 1 gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20191017 MGI PMID:29625069 1558080 Zdhhc15 zinc finger, DHHC domain containing 15 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20111116 MGI 1558080 Zdhhc15 zinc finger, DHHC domain containing 15 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20111116 MGI 1558082 Flnc filamin C, gamma gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1558082 Flnc filamin C, gamma gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20201022 MGI 1558082 Flnc filamin C, gamma gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20170831 MGI PMID:26472074 1558082 Flnc filamin C, gamma gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20201022 MGI 1558082 Flnc filamin C, gamma gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20170831 MGI PMID:26472074 1558082 Flnc filamin C, gamma gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20201022 MGI 1558082 Flnc filamin C, gamma gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20170831 MGI PMID:26472074 1558082 Flnc filamin C, gamma gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20170831 MGI PMID:26472074 1558082 Flnc filamin C, gamma gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20170831 MGI PMID:26472074 1558082 Flnc filamin C, gamma gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0004246 abnormal extensor digitorum longus morphology IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0005534 decreased body temperature IEA N RGD:5509061 20240523 MGI 1558082 Flnc filamin C, gamma gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20170831 MGI PMID:26472074 1558082 Flnc filamin C, gamma gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20170831 MGI PMID:26472074 1558082 Flnc filamin C, gamma gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20170831 MGI PMID:26472074 1558082 Flnc filamin C, gamma gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16914736 1558082 Flnc filamin C, gamma gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558082 Flnc filamin C, gamma gene MP:0011940 decreased food intake IAGP N RGD:5509061 20170831 MGI PMID:26472074 1558082 Flnc filamin C, gamma gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1558084 Rasal2 RAS protein activator like 2 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160225 MGI PMID:24029233 1558084 Rasal2 RAS protein activator like 2 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201022 MGI 1558084 Rasal2 RAS protein activator like 2 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20160225 MGI PMID:24029233 1558084 Rasal2 RAS protein activator like 2 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20160225 MGI PMID:24029233 1558084 Rasal2 RAS protein activator like 2 gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20201022 MGI 1558084 Rasal2 RAS protein activator like 2 gene MP:0002083 premature death IAGP N RGD:5509061 20160225 MGI PMID:24029233 1558084 Rasal2 RAS protein activator like 2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20160225 MGI PMID:24029233 1558084 Rasal2 RAS protein activator like 2 gene MP:0003750 increased mouth tumor incidence IAGP N RGD:5509061 20160225 MGI PMID:24029233 1558084 Rasal2 RAS protein activator like 2 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20170105 MGI 1558084 Rasal2 RAS protein activator like 2 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20160225 MGI PMID:24029233 1558084 Rasal2 RAS protein activator like 2 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20160225 MGI PMID:24029233 1558084 Rasal2 RAS protein activator like 2 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20160225 MGI PMID:24029233 1558084 Rasal2 RAS protein activator like 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160225 MGI PMID:24029233 1558084 Rasal2 RAS protein activator like 2 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:24029233 1558085 Zmat4 zinc finger, matrin type 4 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1558087 Cbx8 chromobox 8 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22094252 1558088 Map7d2 MAP7 domain containing 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1558089 Galns galactosamine (N-acetyl)-6-sulfatase gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:16219627 1558089 Galns galactosamine (N-acetyl)-6-sulfatase gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:14583446 1558089 Galns galactosamine (N-acetyl)-6-sulfatase gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:16219627 1558089 Galns galactosamine (N-acetyl)-6-sulfatase gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16219627 1558089 Galns galactosamine (N-acetyl)-6-sulfatase gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:14583446 1558089 Galns galactosamine (N-acetyl)-6-sulfatase gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:16219627 1558089 Galns galactosamine (N-acetyl)-6-sulfatase gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:16219627 1558089 Galns galactosamine (N-acetyl)-6-sulfatase gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20141003 MGI PMID:16219627 1558089 Galns galactosamine (N-acetyl)-6-sulfatase gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20141003 MGI PMID:17498992 1558089 Galns galactosamine (N-acetyl)-6-sulfatase gene MP:0011473 increased urine glycosaminoglycan level IAGP N RGD:5509061 20141003 MGI PMID:14583446 1558090 Hdac8 histone deacetylase 8 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 1558090 Hdac8 histone deacetylase 8 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19605684 1558090 Hdac8 histone deacetylase 8 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20211230 MGI PMID:30620721 1558090 Hdac8 histone deacetylase 8 gene MP:0001258 decreased body length IEA N RGD:5509061 20160804 MGI 1558090 Hdac8 histone deacetylase 8 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19605684 1558090 Hdac8 histone deacetylase 8 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20211230 MGI PMID:30620721 1558090 Hdac8 histone deacetylase 8 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20211230 MGI PMID:30620721 1558090 Hdac8 histone deacetylase 8 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20211230 MGI PMID:30620721 1558090 Hdac8 histone deacetylase 8 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20230629 MGI PMID:32800293 1558090 Hdac8 histone deacetylase 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19605684 1558090 Hdac8 histone deacetylase 8 gene MP:0003121 genetic imprinting IAGP N RGD:5509061 20141003 MGI PMID:19605684 1558090 Hdac8 histone deacetylase 8 gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20230629 MGI PMID:32800293 1558090 Hdac8 histone deacetylase 8 gene MP:0004378 frontal bone foramen IAGP N RGD:5509061 20141003 MGI PMID:19605684 1558090 Hdac8 histone deacetylase 8 gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20230629 MGI PMID:32800293 1558090 Hdac8 histone deacetylase 8 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20211230 MGI PMID:30620721 1558090 Hdac8 histone deacetylase 8 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20230629 MGI PMID:32800293 1558090 Hdac8 histone deacetylase 8 gene MP:0008276 failure of intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19605684 1558090 Hdac8 histone deacetylase 8 gene MP:0008957 abnormal placenta junctional zone morphology IAGP N RGD:5509061 20230629 MGI PMID:32800293 1558090 Hdac8 histone deacetylase 8 gene MP:0008959 abnormal spongiotrophoblast cell morphology IAGP N RGD:5509061 20230629 MGI PMID:32800293 1558090 Hdac8 histone deacetylase 8 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:19605684 1558090 Hdac8 histone deacetylase 8 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20230629 MGI PMID:32800293 1558090 Hdac8 histone deacetylase 8 gene MP:0010038 abnormal placenta physiology IAGP N RGD:5509061 20230629 MGI PMID:32800293 1558090 Hdac8 histone deacetylase 8 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20141003 MGI 1558090 Hdac8 histone deacetylase 8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20230629 MGI PMID:32800293 1558090 Hdac8 histone deacetylase 8 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19605684 1558090 Hdac8 histone deacetylase 8 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19605684 1558090 Hdac8 histone deacetylase 8 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:32800293 1558092 Arf3 ADP-ribosylation factor 3 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1558092 Arf3 ADP-ribosylation factor 3 gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 1558092 Arf3 ADP-ribosylation factor 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1558092 Arf3 ADP-ribosylation factor 3 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1558092 Arf3 ADP-ribosylation factor 3 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20160811 MGI 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:15148409 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15148409 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15148409 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:15148409 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:17803964 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:17803964 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15148409 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:15148409 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:15148409 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15148409 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:15148409 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:17803964 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:17803964 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0004539 absent maxilla IAGP N RGD:5509061 20141003 MGI PMID:15148409 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17803964 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15148409 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20210128 MGI 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15148409 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:17803964 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15148409 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0011364 abnormal metanephros morphology IAGP N RGD:5509061 20141003 MGI PMID:17803964 1558093 Ctnnbip1 catenin beta interacting protein 1 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17803964 1558094 Gabpb2 GA repeat binding protein, beta 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:18628204 1558094 Gabpb2 GA repeat binding protein, beta 2 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18628204 1558094 Gabpb2 GA repeat binding protein, beta 2 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:18628204 1558094 Gabpb2 GA repeat binding protein, beta 2 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18628204 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0000601 small liver IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558095 C1qtnf2 C1q and tumor necrosis factor related protein 2 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20200310 MGI PMID:31439668 1558096 Dnajc24 DnaJ heat shock protein family (Hsp40) member C24 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:18765564 1558096 Dnajc24 DnaJ heat shock protein family (Hsp40) member C24 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18765564 1558096 Dnajc24 DnaJ heat shock protein family (Hsp40) member C24 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18765564 1558096 Dnajc24 DnaJ heat shock protein family (Hsp40) member C24 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18765564 1558097 Zfx zinc finger protein X-linked gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9187153 1558097 Zfx zinc finger protein X-linked gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:17448993 1558097 Zfx zinc finger protein X-linked gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17448993 1558097 Zfx zinc finger protein X-linked gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9187153 1558097 Zfx zinc finger protein X-linked gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9187153 1558097 Zfx zinc finger protein X-linked gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17448993 1558097 Zfx zinc finger protein X-linked gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:9187153 1558097 Zfx zinc finger protein X-linked gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:9187153 1558097 Zfx zinc finger protein X-linked gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:9187153 1558097 Zfx zinc finger protein X-linked gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:9187153 1558097 Zfx zinc finger protein X-linked gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:9187153 1558097 Zfx zinc finger protein X-linked gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:9187153 1558097 Zfx zinc finger protein X-linked gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:17448993 1558097 Zfx zinc finger protein X-linked gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17448993 1558097 Zfx zinc finger protein X-linked gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17448993 1558097 Zfx zinc finger protein X-linked gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:9187153 1558097 Zfx zinc finger protein X-linked gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17448993 1558097 Zfx zinc finger protein X-linked gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17448993 1558097 Zfx zinc finger protein X-linked gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:9187153 1558097 Zfx zinc finger protein X-linked gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9187153 1558097 Zfx zinc finger protein X-linked gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9187153 1558097 Zfx zinc finger protein X-linked gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17448993 1558097 Zfx zinc finger protein X-linked gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9187153 1558097 Zfx zinc finger protein X-linked gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17448993 1558099 Retnlb resistin like beta gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20190221 MGI PMID:27397737 1558099 Retnlb resistin like beta gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16815164 1558099 Retnlb resistin like beta gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20190221 MGI PMID:27397737 1558099 Retnlb resistin like beta gene MP:0000599 enlarged liver IAGP N RGD:5509061 20190221 MGI PMID:27397737 1558099 Retnlb resistin like beta gene MP:0001260 increased body weight IAGP N RGD:5509061 20190221 MGI PMID:27397737 1558099 Retnlb resistin like beta gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:16815164 1558099 Retnlb resistin like beta gene MP:0001860 liver inflammation IAGP N RGD:5509061 20190221 MGI PMID:27397737 1558099 Retnlb resistin like beta gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17024245 1558099 Retnlb resistin like beta gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20190221 MGI PMID:27397737 1558099 Retnlb resistin like beta gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20190221 MGI PMID:27397737 1558099 Retnlb resistin like beta gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:18802073 1558099 Retnlb resistin like beta gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:17024245 1558099 Retnlb resistin like beta gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20190221 MGI PMID:27397737 1558099 Retnlb resistin like beta gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20190221 MGI PMID:27397737 1558099 Retnlb resistin like beta gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:18802073 1558099 Retnlb resistin like beta gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18802073 1558099 Retnlb resistin like beta gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:16815164 1558099 Retnlb resistin like beta gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:16815164 1558099 Retnlb resistin like beta gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:17024245 1558099 Retnlb resistin like beta gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18802073 1558099 Retnlb resistin like beta gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18802073 1558099 Retnlb resistin like beta gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20190221 MGI PMID:27397737 1558099 Retnlb resistin like beta gene MP:0008608 increased circulating interleukin-13 level IAGP N RGD:5509061 20190221 MGI PMID:27397737 1558099 Retnlb resistin like beta gene MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20240418 MGI PMID:27397737 1558099 Retnlb resistin like beta gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17024245 1558099 Retnlb resistin like beta gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240418 MGI PMID:27397737 1558100 Rspo2 R-spondin 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17904116 1558100 Rspo2 R-spondin 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:17904116 1558100 Rspo2 R-spondin 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:12782276 1558100 Rspo2 R-spondin 2 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:12782276 1558100 Rspo2 R-spondin 2 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12782276 1558100 Rspo2 R-spondin 2 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:18067586 1558100 Rspo2 R-spondin 2 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0000553 absent radius IAGP N RGD:5509061 20141003 MGI PMID:12782276 1558100 Rspo2 R-spondin 2 gene MP:0000553 absent radius IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12782276 1558100 Rspo2 R-spondin 2 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:18067586 1558100 Rspo2 R-spondin 2 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0000561 adactyly IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:17904116 1558100 Rspo2 R-spondin 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:18067586 1558100 Rspo2 R-spondin 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17904116 1558100 Rspo2 R-spondin 2 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:17904116 1558100 Rspo2 R-spondin 2 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:18067586 1558100 Rspo2 R-spondin 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12782276 1558100 Rspo2 R-spondin 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17904116 1558100 Rspo2 R-spondin 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:12782276 1558100 Rspo2 R-spondin 2 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:18067586 1558100 Rspo2 R-spondin 2 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0002256 abnormal laryngeal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:17904116 1558100 Rspo2 R-spondin 2 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0002728 absent tibia IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:12782276 1558100 Rspo2 R-spondin 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:17904116 1558100 Rspo2 R-spondin 2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20220804 MGI PMID:12782276 1558100 Rspo2 R-spondin 2 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:12782276 1558100 Rspo2 R-spondin 2 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:18067586 1558100 Rspo2 R-spondin 2 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17904116 1558100 Rspo2 R-spondin 2 gene MP:0004371 bowed femur IAGP N RGD:5509061 20181011 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0004540 small maxilla IAGP N RGD:5509061 20171019 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0004635 short metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:17904116 1558100 Rspo2 R-spondin 2 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:12782276 1558100 Rspo2 R-spondin 2 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:17904116 1558100 Rspo2 R-spondin 2 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:18067586 1558100 Rspo2 R-spondin 2 gene MP:0005359 growth retardation of incisors IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0005430 absent fibula IAGP N RGD:5509061 20141003 MGI PMID:12782276 1558100 Rspo2 R-spondin 2 gene MP:0005430 absent fibula IAGP N RGD:5509061 20141003 MGI PMID:18067586 1558100 Rspo2 R-spondin 2 gene MP:0005430 absent fibula IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:17904116 1558100 Rspo2 R-spondin 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:18067586 1558100 Rspo2 R-spondin 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17904116 1558100 Rspo2 R-spondin 2 gene MP:0008494 absence of all nails IAGP N RGD:5509061 20141003 MGI PMID:12782276 1558100 Rspo2 R-spondin 2 gene MP:0008494 absence of all nails IAGP N RGD:5509061 20141003 MGI PMID:17904116 1558100 Rspo2 R-spondin 2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0009437 arytenoid and cricoid cartilage fusion IAGP N RGD:5509061 20181108 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:12782276 1558100 Rspo2 R-spondin 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0009895 decreased palatine bone horizontal plate size IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0009898 maxillary shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12782276 1558100 Rspo2 R-spondin 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17904116 1558100 Rspo2 R-spondin 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18067586 1558100 Rspo2 R-spondin 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0011262 abnormal pharyngeal arch mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:19233133 1558100 Rspo2 R-spondin 2 gene MP:0014320 abnormal autopod rotation IAGP N RGD:5509061 20240404 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:22610508 1558100 Rspo2 R-spondin 2 gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20220721 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0030258 small mandibular condyloid process IAGP N RGD:5509061 20171019 MGI PMID:21237142 1558100 Rspo2 R-spondin 2 gene MP:0030302 abnormal maxillary zygomatic process morphology IAGP N RGD:5509061 20171214 MGI PMID:21237142 1558102 Vav3 vav 3 oncogene gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19139088 1558102 Vav3 vav 3 oncogene gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:19139088 1558102 Vav3 vav 3 oncogene gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15848800 1558102 Vav3 vav 3 oncogene gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0001756 abnormal urination IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:19139088 1558102 Vav3 vav 3 oncogene gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:17202406 1558102 Vav3 vav 3 oncogene gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:20140222 1558102 Vav3 vav 3 oncogene gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17158234 1558102 Vav3 vav 3 oncogene gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17158234 1558102 Vav3 vav 3 oncogene gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17202406 1558102 Vav3 vav 3 oncogene gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15848800 1558102 Vav3 vav 3 oncogene gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0003184 increased angiotensin I-converting enzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17202406 1558102 Vav3 vav 3 oncogene gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:16782872 1558102 Vav3 vav 3 oncogene gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:16782872 1558102 Vav3 vav 3 oncogene gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16782872 1558102 Vav3 vav 3 oncogene gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:20140222 1558102 Vav3 vav 3 oncogene gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17202406 1558102 Vav3 vav 3 oncogene gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20141003 MGI PMID:20140222 1558102 Vav3 vav 3 oncogene gene MP:0005497 optic nerve cupping IAGP N RGD:5509061 20141003 MGI PMID:20140222 1558102 Vav3 vav 3 oncogene gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0005582 increased renin activity IAGP N RGD:5509061 20141003 MGI PMID:17202406 1558102 Vav3 vav 3 oncogene gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16782872 1558102 Vav3 vav 3 oncogene gene MP:0005610 increased circulating antidiuretic hormone level IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0005662 increased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0005662 increased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:17202406 1558102 Vav3 vav 3 oncogene gene MP:0005665 increased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0005665 increased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:17202406 1558102 Vav3 vav 3 oncogene gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:20140222 1558102 Vav3 vav 3 oncogene gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17158234 1558102 Vav3 vav 3 oncogene gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:17158234 1558102 Vav3 vav 3 oncogene gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20140222 1558102 Vav3 vav 3 oncogene gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20140222 1558102 Vav3 vav 3 oncogene gene MP:0009274 buphthalmos IAGP N RGD:5509061 20141003 MGI PMID:20140222 1558102 Vav3 vav 3 oncogene gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0009812 abnormal bradykinin level IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:16767097 1558102 Vav3 vav 3 oncogene gene MP:0009922 increased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22683124 1558102 Vav3 vav 3 oncogene gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20150430 MGI PMID:20140222 1558102 Vav3 vav 3 oncogene gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:14623913 1558102 Vav3 vav 3 oncogene gene MP:0031232 increased circulating angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:16767097 1558103 Blnk B cell linker gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210826 MGI 1558103 Blnk B cell linker gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210826 MGI 1558103 Blnk B cell linker gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12436112 1558103 Blnk B cell linker gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12818163 1558103 Blnk B cell linker gene MP:0000692 small spleen IEA N RGD:5509061 20210826 MGI 1558103 Blnk B cell linker gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16585562 1558103 Blnk B cell linker gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12818163 1558103 Blnk B cell linker gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10583957 1558103 Blnk B cell linker gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10591180 1558103 Blnk B cell linker gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11449370 1558103 Blnk B cell linker gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12818163 1558103 Blnk B cell linker gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22761313 1558103 Blnk B cell linker gene MP:0001805 decreased IgG level IEA N RGD:5509061 20111116 MGI 1558103 Blnk B cell linker gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10591180 1558103 Blnk B cell linker gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15331445 1558103 Blnk B cell linker gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1558103 Blnk B cell linker gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12436112 1558103 Blnk B cell linker gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15331445 1558103 Blnk B cell linker gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:12818163 1558103 Blnk B cell linker gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10583957 1558103 Blnk B cell linker gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10700474 1558103 Blnk B cell linker gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12119344 1558103 Blnk B cell linker gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12818163 1558103 Blnk B cell linker gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15331445 1558103 Blnk B cell linker gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16585562 1558103 Blnk B cell linker gene MP:0002403 abnormal pre-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10591180 1558103 Blnk B cell linker gene MP:0002403 abnormal pre-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12818163 1558103 Blnk B cell linker gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12618482 1558103 Blnk B cell linker gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:10583957 1558103 Blnk B cell linker gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15331445 1558103 Blnk B cell linker gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0002607 decreased basophil cell number IEA N RGD:5509061 20210826 MGI 1558103 Blnk B cell linker gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10591180 1558103 Blnk B cell linker gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12119344 1558103 Blnk B cell linker gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12436112 1558103 Blnk B cell linker gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:15528332 1558103 Blnk B cell linker gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20210826 MGI 1558103 Blnk B cell linker gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20210826 MGI 1558103 Blnk B cell linker gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210826 MGI 1558103 Blnk B cell linker gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10700474 1558103 Blnk B cell linker gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12119344 1558103 Blnk B cell linker gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16585562 1558103 Blnk B cell linker gene MP:0005022 abnormal immature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15528332 1558103 Blnk B cell linker gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10700474 1558103 Blnk B cell linker gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12618482 1558103 Blnk B cell linker gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20111116 MGI 1558103 Blnk B cell linker gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20111116 MGI 1558103 Blnk B cell linker gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:10583957 1558103 Blnk B cell linker gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10583957 1558103 Blnk B cell linker gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10583957 1558103 Blnk B cell linker gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10700474 1558103 Blnk B cell linker gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16585562 1558103 Blnk B cell linker gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:12119344 1558103 Blnk B cell linker gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0008203 absent B-1a cells IAGP N RGD:5509061 20141003 MGI PMID:10700474 1558103 Blnk B cell linker gene MP:0008204 absent B-1b cells IAGP N RGD:5509061 20141003 MGI PMID:10583957 1558103 Blnk B cell linker gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10700474 1558103 Blnk B cell linker gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12119344 1558103 Blnk B cell linker gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12818163 1558103 Blnk B cell linker gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:20133609 1558103 Blnk B cell linker gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10583957 1558103 Blnk B cell linker gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10591180 1558103 Blnk B cell linker gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10700474 1558103 Blnk B cell linker gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12818163 1558103 Blnk B cell linker gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15331445 1558103 Blnk B cell linker gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:12818163 1558103 Blnk B cell linker gene MP:0008213 absent immature B cells IAGP N RGD:5509061 20141003 MGI PMID:12818163 1558103 Blnk B cell linker gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10700474 1558103 Blnk B cell linker gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12818163 1558103 Blnk B cell linker gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15331445 1558103 Blnk B cell linker gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:10700474 1558103 Blnk B cell linker gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:16585562 1558103 Blnk B cell linker gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:10591180 1558103 Blnk B cell linker gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:15331445 1558103 Blnk B cell linker gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0008781 abnormal B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16481047 1558103 Blnk B cell linker gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16585562 1558103 Blnk B cell linker gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20190509 MGI PMID:24888588 1558103 Blnk B cell linker gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:10583957 1558103 Blnk B cell linker gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16585562 1558106 Neto1 neuropilin (NRP) and tolloid (TLL)-like 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19243221 1558106 Neto1 neuropilin (NRP) and tolloid (TLL)-like 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:19243221 1558106 Neto1 neuropilin (NRP) and tolloid (TLL)-like 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:19243221 1558106 Neto1 neuropilin (NRP) and tolloid (TLL)-like 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19243221 1558106 Neto1 neuropilin (NRP) and tolloid (TLL)-like 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21623363 1558106 Neto1 neuropilin (NRP) and tolloid (TLL)-like 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21734292 1558106 Neto1 neuropilin (NRP) and tolloid (TLL)-like 1 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:21623363 1558106 Neto1 neuropilin (NRP) and tolloid (TLL)-like 1 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20180412 MGI PMID:25126785 1558106 Neto1 neuropilin (NRP) and tolloid (TLL)-like 1 gene MP:0009244 abnormal acid-activated cation-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:21623363 1558106 Neto1 neuropilin (NRP) and tolloid (TLL)-like 1 gene MP:0011274 short excitatory postsynaptic current decay time IAGP N RGD:5509061 20240418 MGI PMID:21734292 1558109 Tcf20 transcription factor 20 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20210812 MGI PMID:32510763 1558109 Tcf20 transcription factor 20 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20210812 MGI PMID:32510763 1558109 Tcf20 transcription factor 20 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20210812 MGI PMID:32510763 1558109 Tcf20 transcription factor 20 gene MP:0001258 decreased body length IEA N RGD:5509061 20201022 MGI 1558109 Tcf20 transcription factor 20 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210812 MGI PMID:32510763 1558109 Tcf20 transcription factor 20 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20210812 MGI PMID:32510763 1558109 Tcf20 transcription factor 20 gene MP:0001394 circling IAGP N RGD:5509061 20210812 MGI PMID:32510763 1558109 Tcf20 transcription factor 20 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20210812 MGI PMID:32510763 1558109 Tcf20 transcription factor 20 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210812 MGI PMID:32510763 1558109 Tcf20 transcription factor 20 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20201022 MGI 1558109 Tcf20 transcription factor 20 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 1558109 Tcf20 transcription factor 20 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1558109 Tcf20 transcription factor 20 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1558109 Tcf20 transcription factor 20 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20210812 MGI PMID:32510763 1558109 Tcf20 transcription factor 20 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1558109 Tcf20 transcription factor 20 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 1558109 Tcf20 transcription factor 20 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 1558109 Tcf20 transcription factor 20 gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20210812 MGI PMID:32510763 1558109 Tcf20 transcription factor 20 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210812 MGI PMID:32510763 1558109 Tcf20 transcription factor 20 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20210812 MGI PMID:32510763 1558109 Tcf20 transcription factor 20 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20210812 MGI PMID:32510763 1558111 Sh3rf3 SH3 domain containing ring finger 3 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20240523 MGI 1558112 Lsm1 LSM1 homolog, mRNA degradation associated gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1558112 Lsm1 LSM1 homolog, mRNA degradation associated gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 1558112 Lsm1 LSM1 homolog, mRNA degradation associated gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1558112 Lsm1 LSM1 homolog, mRNA degradation associated gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1558112 Lsm1 LSM1 homolog, mRNA degradation associated gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20210128 MGI 1558112 Lsm1 LSM1 homolog, mRNA degradation associated gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1558112 Lsm1 LSM1 homolog, mRNA degradation associated gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20220811 MGI 1558112 Lsm1 LSM1 homolog, mRNA degradation associated gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1558112 Lsm1 LSM1 homolog, mRNA degradation associated gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1558112 Lsm1 LSM1 homolog, mRNA degradation associated gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1558112 Lsm1 LSM1 homolog, mRNA degradation associated gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160421 MGI 1558112 Lsm1 LSM1 homolog, mRNA degradation associated gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220811 MGI 1558112 Lsm1 LSM1 homolog, mRNA degradation associated gene MP:0010574 dilated aorta IEA N RGD:5509061 20160421 MGI 1558112 Lsm1 LSM1 homolog, mRNA degradation associated gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558113 Il17rd interleukin 17 receptor D gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17442811 1558113 Il17rd interleukin 17 receptor D gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15729686 1558113 Il17rd interleukin 17 receptor D gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20210520 MGI 1558113 Il17rd interleukin 17 receptor D gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17442811 1558113 Il17rd interleukin 17 receptor D gene MP:0012490 abnormal cochlear VIII nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:17442811 1558114 Zfp341 zinc finger protein 341 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20181227 MGI 1558114 Zfp341 zinc finger protein 341 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1558114 Zfp341 zinc finger protein 341 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1558114 Zfp341 zinc finger protein 341 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 1558117 Lbx2 ladybird homeobox 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17492753 1558117 Lbx2 ladybird homeobox 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17492753 1558117 Lbx2 ladybird homeobox 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17492753 1558117 Lbx2 ladybird homeobox 2 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:17492753 1558117 Lbx2 ladybird homeobox 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17492753 1558117 Lbx2 ladybird homeobox 2 gene MP:0010768 mortality/aging IAGP N RGD:5509061 20201029 MGI PMID:17492753 1558118 Wasf1 WASP family, member 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12578964 1558118 Wasf1 WASP family, member 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12578964 1558118 Wasf1 WASP family, member 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12578964 1558118 Wasf1 WASP family, member 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:12578964 1558118 Wasf1 WASP family, member 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12578964 1558118 Wasf1 WASP family, member 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17215396 1558118 Wasf1 WASP family, member 1 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:17215396 1558118 Wasf1 WASP family, member 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:12578964 1558118 Wasf1 WASP family, member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12578964 1558118 Wasf1 WASP family, member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17215396 1558118 Wasf1 WASP family, member 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17215396 1558118 Wasf1 WASP family, member 1 gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17215396 1558118 Wasf1 WASP family, member 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:17215396 1558118 Wasf1 WASP family, member 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17215396 1558118 Wasf1 WASP family, member 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:17215396 1558118 Wasf1 WASP family, member 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:17215396 1558118 Wasf1 WASP family, member 1 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0008109 abnormal small intestinal microvillus morphology IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:12716942 1558118 Wasf1 WASP family, member 1 gene MP:0012489 abnormal retrosplenial region morphology IAGP N RGD:5509061 20141003 MGI PMID:12716942 1558121 Usp10 ubiquitin specific peptidase 10 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23230274 1558121 Usp10 ubiquitin specific peptidase 10 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23230274 1558121 Usp10 ubiquitin specific peptidase 10 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23230274 1558121 Usp10 ubiquitin specific peptidase 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558122 Sirt2 sirtuin 2 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20160804 MGI 1558122 Sirt2 sirtuin 2 gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22014574 1558122 Sirt2 sirtuin 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:21949390 1558122 Sirt2 sirtuin 2 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:23364049 1558122 Sirt2 sirtuin 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20141003 MGI 1558122 Sirt2 sirtuin 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22511966 1558122 Sirt2 sirtuin 2 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23468428 1558122 Sirt2 sirtuin 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22014574 1558122 Sirt2 sirtuin 2 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22014574 1558122 Sirt2 sirtuin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23364049 1558122 Sirt2 sirtuin 2 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:23468428 1558122 Sirt2 sirtuin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21949390 1558122 Sirt2 sirtuin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160915 MGI PMID:24652767 1558122 Sirt2 sirtuin 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:22511966 1558122 Sirt2 sirtuin 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:23468428 1558122 Sirt2 sirtuin 2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22014574 1558122 Sirt2 sirtuin 2 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:23468428 1558122 Sirt2 sirtuin 2 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:22014574 1558122 Sirt2 sirtuin 2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:22014574 1558122 Sirt2 sirtuin 2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:23468428 1558122 Sirt2 sirtuin 2 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:21949390 1558122 Sirt2 sirtuin 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20141003 MGI 1558122 Sirt2 sirtuin 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:23364049 1558122 Sirt2 sirtuin 2 gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:22014574 1558122 Sirt2 sirtuin 2 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22014574 1558122 Sirt2 sirtuin 2 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:21949390 1558122 Sirt2 sirtuin 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23364049 1558122 Sirt2 sirtuin 2 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22014574 1558122 Sirt2 sirtuin 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23468428 1558122 Sirt2 sirtuin 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:22511966 1558122 Sirt2 sirtuin 2 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22014574 1558122 Sirt2 sirtuin 2 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22014574 1558122 Sirt2 sirtuin 2 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22014574 1558122 Sirt2 sirtuin 2 gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22014574 1558122 Sirt2 sirtuin 2 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22014574 1558125 Coasy Coenzyme A synthase gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230119 MGI 1558125 Coasy Coenzyme A synthase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210128 MGI PMID:33352696 1558125 Coasy Coenzyme A synthase gene MP:0001391 abnormal tail movements IAGP N RGD:5509061 20210128 MGI PMID:33352696 1558125 Coasy Coenzyme A synthase gene MP:0001523 impaired righting response IAGP N RGD:5509061 20210128 MGI PMID:33352696 1558125 Coasy Coenzyme A synthase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210128 MGI PMID:33352696 1558125 Coasy Coenzyme A synthase gene MP:0002083 premature death IAGP N RGD:5509061 20210128 MGI PMID:33352696 1558125 Coasy Coenzyme A synthase gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20210128 MGI PMID:33352696 1558125 Coasy Coenzyme A synthase gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 1558125 Coasy Coenzyme A synthase gene MP:0005323 dystonia IAGP N RGD:5509061 20210128 MGI PMID:33352696 1558125 Coasy Coenzyme A synthase gene MP:0005356 positive geotaxis IAGP N RGD:5509061 20210128 MGI PMID:33352696 1558125 Coasy Coenzyme A synthase gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20230119 MGI 1558125 Coasy Coenzyme A synthase gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20210128 MGI PMID:33352696 1558125 Coasy Coenzyme A synthase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1558125 Coasy Coenzyme A synthase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230601 MGI 1558125 Coasy Coenzyme A synthase gene MP:0020365 increased brain iron level IAGP N RGD:5509061 20210128 MGI PMID:33352696 1558125 Coasy Coenzyme A synthase gene MP:0020879 abnormal calcium level IAGP N RGD:5509061 20210128 MGI PMID:33352696 1558125 Coasy Coenzyme A synthase gene MP:0020883 abnormal magnesium level IAGP N RGD:5509061 20210128 MGI PMID:33352696 1558126 Zfp711 zinc finger protein 711 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1558128 Evx1 even-skipped homeobox 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7958869 1558128 Evx1 even-skipped homeobox 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7958869 1558128 Evx1 even-skipped homeobox 1 gene MP:0012102 absent trophectoderm IAGP N RGD:5509061 20141003 MGI PMID:7958869 1558128 Evx1 even-skipped homeobox 1 gene MP:0021102 abnormal ventral interneuron 0 morphology IAGP N RGD:5509061 20220310 MGI PMID:11239430 1558129 Tal2 T cell acute lymphocytic leukemia 2 gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:11071772 1558129 Tal2 T cell acute lymphocytic leukemia 2 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:11071772 1558129 Tal2 T cell acute lymphocytic leukemia 2 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:11071772 1558129 Tal2 T cell acute lymphocytic leukemia 2 gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:11071772 1558129 Tal2 T cell acute lymphocytic leukemia 2 gene MP:0000917 obstructive hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:11071772 1558129 Tal2 T cell acute lymphocytic leukemia 2 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:11071772 1558129 Tal2 T cell acute lymphocytic leukemia 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11071772 1558129 Tal2 T cell acute lymphocytic leukemia 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11071772 1558129 Tal2 T cell acute lymphocytic leukemia 2 gene MP:0002892 decreased superior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:11071772 1558129 Tal2 T cell acute lymphocytic leukemia 2 gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20141003 MGI PMID:11071772 1558129 Tal2 T cell acute lymphocytic leukemia 2 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11071772 1558129 Tal2 T cell acute lymphocytic leukemia 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1558130 Nsun4 NOL1/NOP2/Sun domain family, member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20190509 MGI PMID:24516400 1558130 Nsun4 NOL1/NOP2/Sun domain family, member 4 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20190509 MGI PMID:24516400 1558130 Nsun4 NOL1/NOP2/Sun domain family, member 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20190509 MGI PMID:24516400 1558130 Nsun4 NOL1/NOP2/Sun domain family, member 4 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20190509 MGI PMID:24516400 1558130 Nsun4 NOL1/NOP2/Sun domain family, member 4 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20190509 MGI PMID:24516400 1558130 Nsun4 NOL1/NOP2/Sun domain family, member 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20190509 MGI PMID:24516400 1558130 Nsun4 NOL1/NOP2/Sun domain family, member 4 gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20240718 MGI PMID:24516400 1558131 Coq9 coenzyme Q9 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0005114 premature hair loss IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558131 Coq9 coenzyme Q9 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:23255162 1558132 Slfn8 schlafen 8 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20210429 MGI PMID:29528433 1558132 Slfn8 schlafen 8 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20210429 MGI PMID:29528433 1558132 Slfn8 schlafen 8 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20210429 MGI PMID:29528433 1558132 Slfn8 schlafen 8 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20210429 MGI PMID:29528433 1558132 Slfn8 schlafen 8 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20210429 MGI PMID:29528433 1558133 Iqcf1 IQ motif containing F1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20160324 MGI PMID:25380116 1558133 Iqcf1 IQ motif containing F1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20160324 MGI PMID:25380116 1558133 Iqcf1 IQ motif containing F1 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20160324 MGI PMID:25380116 1558133 Iqcf1 IQ motif containing F1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210826 MGI 1558134 Lrsam1 leucine rich repeat and sterile alpha motif containing 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:23519028 1558134 Lrsam1 leucine rich repeat and sterile alpha motif containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23519028 1558134 Lrsam1 leucine rich repeat and sterile alpha motif containing 1 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:23519028 1558134 Lrsam1 leucine rich repeat and sterile alpha motif containing 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:23519028 1558134 Lrsam1 leucine rich repeat and sterile alpha motif containing 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:23519028 1558134 Lrsam1 leucine rich repeat and sterile alpha motif containing 1 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20231207 MGI 1558134 Lrsam1 leucine rich repeat and sterile alpha motif containing 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:23519028 1558134 Lrsam1 leucine rich repeat and sterile alpha motif containing 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1558135 Rnf128 ring finger protein 128 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20201022 MGI 1558135 Rnf128 ring finger protein 128 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20180719 MGI PMID:28581443 1558135 Rnf128 ring finger protein 128 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0005000 abnormal immune tolerance IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19805371 1558135 Rnf128 ring finger protein 128 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19805371 1558135 Rnf128 ring finger protein 128 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19805371 1558135 Rnf128 ring finger protein 128 gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19805371 1558135 Rnf128 ring finger protein 128 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0008599 increased circulating interleukin-2 level IAGP N RGD:5509061 20141003 MGI PMID:19805371 1558135 Rnf128 ring finger protein 128 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0008749 abnormal peripheral T cell anergy IAGP N RGD:5509061 20141003 MGI PMID:19805371 1558135 Rnf128 ring finger protein 128 gene MP:0009057 increased interleukin-21 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20493730 1558135 Rnf128 ring finger protein 128 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20201022 MGI 1558135 Rnf128 ring finger protein 128 gene MP:0012564 decreased tumor incidence following infection IAGP N RGD:5509061 20241114 MGI PMID:36103821 1558135 Rnf128 ring finger protein 128 gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20211021 MGI 1558136 Elp4 elongator acetyltransferase complex subunit 4 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20240523 MGI 1558136 Elp4 elongator acetyltransferase complex subunit 4 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20240523 MGI 1558136 Elp4 elongator acetyltransferase complex subunit 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0001926 female infertility IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0001935 decreased litter size IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0004025 polyploidy IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558137 Ercc6l excision repair cross-complementing rodent repair deficiency complementation group 6 like gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20190328 MGI PMID:30232008 1558139 Dkk2 dickkopf WNT signaling pathway inhibitor 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16056226 1558139 Dkk2 dickkopf WNT signaling pathway inhibitor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16672341 1558139 Dkk2 dickkopf WNT signaling pathway inhibitor 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:16672341 1558139 Dkk2 dickkopf WNT signaling pathway inhibitor 2 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16056226 1558139 Dkk2 dickkopf WNT signaling pathway inhibitor 2 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:16056226 1558139 Dkk2 dickkopf WNT signaling pathway inhibitor 2 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16672341 1558139 Dkk2 dickkopf WNT signaling pathway inhibitor 2 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:16056226 1558139 Dkk2 dickkopf WNT signaling pathway inhibitor 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:16056226 1558139 Dkk2 dickkopf WNT signaling pathway inhibitor 2 gene MP:0013754 abnormal ocular surface morphology IAGP N RGD:5509061 20150416 MGI PMID:16672341 1558139 Dkk2 dickkopf WNT signaling pathway inhibitor 2 gene MP:0020857 cornea epithelium hyperplasia IAGP N RGD:5509061 20181101 MGI PMID:16672341 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16407979 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16407979 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0000794 abnormal parietal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:16407979 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0000798 abnormal frontal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:16407979 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:16407979 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:16407979 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16407979 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16407979 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16407979 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:16407979 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:16407979 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20181004 MGI 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0005623 abnormal meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:16407979 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0005630 increased lung weight IEA N RGD:5509061 20230601 MGI 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0009026 abnormal brain pia mater morphology IAGP N RGD:5509061 20141003 MGI PMID:16407979 1558141 Apbb2 amyloid beta precursor protein binding family B member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:19357712 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0000420 ruffled hair IEA N RGD:5509061 20160324 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:19357712 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20151001 MGI PMID:25128525 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0000919 cranioschisis IAGP N RGD:5509061 20141003 MGI PMID:19357712 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:12842012 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20151001 MGI PMID:25128525 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220519 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001148 enlarged testis IEA N RGD:5509061 20220519 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:20223754 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20223754 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001265 decreased body size IEA N RGD:5509061 20160324 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001304 cataract IEA N RGD:5509061 20220519 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20151001 MGI PMID:25128525 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001341 absent eyelids IAGP N RGD:5509061 20141003 MGI PMID:12842012 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001394 circling IEA N RGD:5509061 20160324 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20230601 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:10932191 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001411 spinning IAGP N RGD:5509061 20141003 MGI PMID:12842012 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20160324 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20151001 MGI PMID:25128525 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001850 increased susceptibility to otitis media IEA N RGD:5509061 20160324 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20160324 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001921 reduced fertility IEA N RGD:5509061 20160324 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001925 male infertility IEA N RGD:5509061 20220811 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001926 female infertility IEA N RGD:5509061 20220811 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0001967 deafness IEA N RGD:5509061 20160324 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20160324 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20151001 MGI PMID:25128525 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20151001 MGI PMID:25128525 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20220519 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20151001 MGI PMID:25128525 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:12842012 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0002730 head shaking IAGP N RGD:5509061 20151001 MGI PMID:25128525 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20151001 MGI PMID:25128525 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20151001 MGI PMID:25128525 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:20704721 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20151001 MGI PMID:25128525 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0003205 testicular atrophy IEA N RGD:5509061 20160324 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20151001 MGI PMID:25128525 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12842012 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:10932191 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:20223754 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:19357712 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0004300 abnormal organ of Corti supporting cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12842012 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0004391 abnormal respiratory conducting tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20223754 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12842012 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:12842012 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0005238 increased brain size IEA N RGD:5509061 20220519 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0005307 head tossing IEA N RGD:5509061 20160324 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20151001 MGI PMID:25128525 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0006026 dilated terminal bronchiole tube IAGP N RGD:5509061 20141003 MGI PMID:20223754 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0006325 impaired hearing IEA N RGD:5509061 20160324 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20223754 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:12842012 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20151001 MGI PMID:25128525 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0009457 whorled hair IAGP N RGD:5509061 20141003 MGI PMID:19357712 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20151001 MGI PMID:25128525 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:20223754 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:20223754 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0010976 small lung lobe IAGP N RGD:5509061 20141003 MGI PMID:20223754 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:20223754 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0011032 impaired branching involved in terminal bronchiole morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:20223754 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12842012 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19357712 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:20223754 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20160324 MGI 1558142 Celsr1 cadherin, EGF LAG seven-pass G-type receptor 1 gene MP:0030961 abnormal outer hair cell kinocilium location or orientation IAGP N RGD:5509061 20190725 MGI PMID:12842012 1558143 Rbmx RNA binding motif protein, X chromosome gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 1558143 Rbmx RNA binding motif protein, X chromosome gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 1558143 Rbmx RNA binding motif protein, X chromosome gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1558143 Rbmx RNA binding motif protein, X chromosome gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1558143 Rbmx RNA binding motif protein, X chromosome gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 1558143 Rbmx RNA binding motif protein, X chromosome gene MP:0003917 increased kidney weight IEA N RGD:5509061 20210128 MGI 1558143 Rbmx RNA binding motif protein, X chromosome gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20562862 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22556408 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20562862 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20525685 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20562862 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:20525685 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20363774 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20525685 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:22556408 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20151119 MGI PMID:23448972 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20525685 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001935 decreased litter size IAGP N RGD:5509061 20151119 MGI PMID:23448972 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20695981 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20151119 MGI PMID:23448972 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20562862 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20562862 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20562862 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:20363774 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:22556408 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20562862 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:20695981 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20151119 MGI PMID:23448972 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:20363774 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:20525685 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0008247 abnormal mononuclear cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20562862 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:20525685 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0010022 brain vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:20562862 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0010197 abnormal lymphatic vessel endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0010198 decreased lymphatic vessel endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0010368 abnormal lymphatic system physiology IAGP N RGD:5509061 20141003 MGI PMID:20525685 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20525685 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20695981 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20562862 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20695981 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20525685 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20562862 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0011514 skin hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0011898 abnormal platelet cell number IAGP N RGD:5509061 20151119 MGI PMID:23448972 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0012080 chylous ascites IAGP N RGD:5509061 20141003 MGI PMID:22186994 1558144 Clec1b C-type lectin domain family 1, member b gene MP:0031051 lymph node hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:23995678 1558145 Rab33a RAB33A, member RAS oncogene family gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20221215 MGI 1558146 Tceal1 transcription elongation factor A (SII)-like 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20190502 MGI 1558146 Tceal1 transcription elongation factor A (SII)-like 1 gene MP:0002989 small kidney IEA N RGD:5509061 20190502 MGI 1558146 Tceal1 transcription elongation factor A (SII)-like 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1558146 Tceal1 transcription elongation factor A (SII)-like 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1558147 H2-Eb1 histocompatibility 2, class II antigen E beta gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20231207 MGI 1558148 Fmr1nb Fmr1 neighbor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1558149 Zfp61 zinc finger protein 61 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 1558149 Zfp61 zinc finger protein 61 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210520 MGI 1558149 Zfp61 zinc finger protein 61 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20181227 MGI 1558152 Kdm5c lysine demethylase 5C gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20111116 MGI 1558152 Kdm5c lysine demethylase 5C gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180712 MGI PMID:26804915 1558152 Kdm5c lysine demethylase 5C gene MP:0001265 decreased body size IAGP N RGD:5509061 20180712 MGI PMID:26804915 1558152 Kdm5c lysine demethylase 5C gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20180712 MGI PMID:26804915 1558152 Kdm5c lysine demethylase 5C gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20180712 MGI PMID:26804915 1558152 Kdm5c lysine demethylase 5C gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20180712 MGI PMID:26804915 1558152 Kdm5c lysine demethylase 5C gene MP:0002084 abnormal developmental patterning IEA N RGD:5509061 20111116 MGI 1558152 Kdm5c lysine demethylase 5C gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1558152 Kdm5c lysine demethylase 5C gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20180712 MGI PMID:26804915 1558152 Kdm5c lysine demethylase 5C gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20180712 MGI PMID:26804915 1558152 Kdm5c lysine demethylase 5C gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20180712 MGI PMID:26804915 1558152 Kdm5c lysine demethylase 5C gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20180712 MGI PMID:26804915 1558152 Kdm5c lysine demethylase 5C gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20180712 MGI PMID:26804915 1558152 Kdm5c lysine demethylase 5C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20221222 MGI 1558152 Kdm5c lysine demethylase 5C gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20180712 MGI PMID:26804915 1558152 Kdm5c lysine demethylase 5C gene MP:0020337 abnormal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20180712 MGI PMID:26804915 1558152 Kdm5c lysine demethylase 5C gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20180712 MGI PMID:26804915 1558152 Kdm5c lysine demethylase 5C gene MP:0020512 abnormal dendritic mushroom spine morphology IAGP N RGD:5509061 20180712 MGI PMID:26804915 1558154 Appl2 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20160519 MGI PMID:26445298 1558154 Appl2 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20160519 MGI PMID:26445298 1558154 Appl2 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20160505 MGI PMID:24879834 1558154 Appl2 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20160505 MGI PMID:24879834 1558154 Appl2 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20160519 MGI PMID:26445298 1558154 Appl2 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20160519 MGI PMID:26445298 1558154 Appl2 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20160519 MGI PMID:26445298 1558154 Appl2 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 2 gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:24879834 1558155 H2ax H2A.X variant histone gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11934988 1558155 H2ax H2A.X variant histone gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19377486 1558155 H2ax H2A.X variant histone gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11934988 1558155 H2ax H2A.X variant histone gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:11934988 1558155 H2ax H2A.X variant histone gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12914700 1558155 H2ax H2A.X variant histone gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:11934988 1558155 H2ax H2A.X variant histone gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11934988 1558155 H2ax H2A.X variant histone gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11740565 1558155 H2ax H2A.X variant histone gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12914700 1558155 H2ax H2A.X variant histone gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:12914701 1558155 H2ax H2A.X variant histone gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12914700 1558155 H2ax H2A.X variant histone gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12914700 1558155 H2ax H2A.X variant histone gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12914700 1558155 H2ax H2A.X variant histone gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12914700 1558155 H2ax H2A.X variant histone gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12914701 1558155 H2ax H2A.X variant histone gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12914700 1558155 H2ax H2A.X variant histone gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:19377486 1558155 H2ax H2A.X variant histone gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:19377486 1558155 H2ax H2A.X variant histone gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:18599436 1558155 H2ax H2A.X variant histone gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:12810694 1558155 H2ax H2A.X variant histone gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:12914700 1558155 H2ax H2A.X variant histone gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:23254285 1558155 H2ax H2A.X variant histone gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12914700 1558155 H2ax H2A.X variant histone gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11934988 1558155 H2ax H2A.X variant histone gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11934988 1558155 H2ax H2A.X variant histone gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:11934988 1558155 H2ax H2A.X variant histone gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:19377486 1558155 H2ax H2A.X variant histone gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:12914700 1558155 H2ax H2A.X variant histone gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:18599436 1558155 H2ax H2A.X variant histone gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12914700 1558155 H2ax H2A.X variant histone gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:19377486 1558155 H2ax H2A.X variant histone gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18599436 1558155 H2ax H2A.X variant histone gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12914700 1558155 H2ax H2A.X variant histone gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12914701 1558155 H2ax H2A.X variant histone gene MP:0012556 increased cell death IAGP N RGD:5509061 20150212 MGI PMID:18599436 1558155 H2ax H2A.X variant histone gene MP:0020316 decreased vascular endothelial cell proliferation IAGP N RGD:5509061 20160616 MGI PMID:23254285 1558155 H2ax H2A.X variant histone gene MP:0020321 increased vascular endothelial cell apoptosis IAGP N RGD:5509061 20160616 MGI PMID:19377486 1558156 Emcn endomucin gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20201022 MGI 1558156 Emcn endomucin gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20181227 MGI 1558156 Emcn endomucin gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1558156 Emcn endomucin gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20181227 MGI 1558156 Emcn endomucin gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20181227 MGI 1558156 Emcn endomucin gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200402 MGI 1558156 Emcn endomucin gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1558157 Atxn7 ataxin 7 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16494529 1558157 Atxn7 ataxin 7 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16494529 1558157 Atxn7 ataxin 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0002922 decreased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1558157 Atxn7 ataxin 7 gene MP:0010387 abnormal Bergmann glial cell morphology IAGP N RGD:5509061 20180830 MGI PMID:16936724 1558157 Atxn7 ataxin 7 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22002997 1558157 Atxn7 ataxin 7 gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:12575948 1558157 Atxn7 ataxin 7 gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:22002997 1558159 Apip APAF1 interacting protein gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20201022 MGI 1558161 Dnmbp dynamin binding protein gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1558161 Dnmbp dynamin binding protein gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1558161 Dnmbp dynamin binding protein gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1558161 Dnmbp dynamin binding protein gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1558161 Dnmbp dynamin binding protein gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230601 MGI 1558161 Dnmbp dynamin binding protein gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1558161 Dnmbp dynamin binding protein gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1558161 Dnmbp dynamin binding protein gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1558161 Dnmbp dynamin binding protein gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1558161 Dnmbp dynamin binding protein gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 1558161 Dnmbp dynamin binding protein gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20201022 MGI 1558161 Dnmbp dynamin binding protein gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20201022 MGI 1558161 Dnmbp dynamin binding protein gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1558161 Dnmbp dynamin binding protein gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20190502 MGI 1558162 Plxna3 plexin A3 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:11683995 1558162 Plxna3 plexin A3 gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:11683995 1558162 Plxna3 plexin A3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15721238 1558162 Plxna3 plexin A3 gene MP:0001063 abnormal trochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15721238 1558162 Plxna3 plexin A3 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11683995 1558162 Plxna3 plexin A3 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15721238 1558162 Plxna3 plexin A3 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11683995 1558162 Plxna3 plexin A3 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12732138 1558162 Plxna3 plexin A3 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:11683995 1558162 Plxna3 plexin A3 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15721238 1558162 Plxna3 plexin A3 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1558162 Plxna3 plexin A3 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1558162 Plxna3 plexin A3 gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1558162 Plxna3 plexin A3 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1558162 Plxna3 plexin A3 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1558162 Plxna3 plexin A3 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1558162 Plxna3 plexin A3 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:21835343 1558162 Plxna3 plexin A3 gene MP:0008960 abnormal axon pruning IAGP N RGD:5509061 20141003 MGI PMID:12732138 1558163 Hoxb6 homeobox B6 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7828847 1558163 Hoxb6 homeobox B6 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:7828847 1558163 Hoxb6 homeobox B6 gene MP:0000152 absent proximal rib IAGP N RGD:5509061 20141003 MGI PMID:7828847 1558163 Hoxb6 homeobox B6 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:7828847 1558163 Hoxb6 homeobox B6 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:17626057 1558163 Hoxb6 homeobox B6 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:10996827 1558163 Hoxb6 homeobox B6 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10996827 1558163 Hoxb6 homeobox B6 gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:7828847 1558163 Hoxb6 homeobox B6 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:10996827 1558163 Hoxb6 homeobox B6 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1558163 Hoxb6 homeobox B6 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7828847 1558163 Hoxb6 homeobox B6 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:10996827 1558163 Hoxb6 homeobox B6 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:17626057 1558163 Hoxb6 homeobox B6 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:7828847 1558163 Hoxb6 homeobox B6 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:17626057 1558163 Hoxb6 homeobox B6 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1558163 Hoxb6 homeobox B6 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1558163 Hoxb6 homeobox B6 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7828847 1558163 Hoxb6 homeobox B6 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1558163 Hoxb6 homeobox B6 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7828847 1558163 Hoxb6 homeobox B6 gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1558163 Hoxb6 homeobox B6 gene MP:0004680 small xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:17626057 1558163 Hoxb6 homeobox B6 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1558163 Hoxb6 homeobox B6 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:17626057 1558165 Cep41 centrosomal protein 41 gene MP:0000288 abnormal pericardium morphology IAGP N RGD:5509061 20141003 MGI PMID:22246503 1558165 Cep41 centrosomal protein 41 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:22246503 1558165 Cep41 centrosomal protein 41 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22246503 1558165 Cep41 centrosomal protein 41 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:22246503 1558165 Cep41 centrosomal protein 41 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22246503 1558165 Cep41 centrosomal protein 41 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1558165 Cep41 centrosomal protein 41 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22246503 1558166 Mindy1 MINDY lysine 48 deubiquitinase 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1558166 Mindy1 MINDY lysine 48 deubiquitinase 1 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20160804 MGI 1558166 Mindy1 MINDY lysine 48 deubiquitinase 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1558166 Mindy1 MINDY lysine 48 deubiquitinase 1 gene MP:0003313 abnormal locomotor activation IEA N RGD:5509061 20141003 MGI 1558166 Mindy1 MINDY lysine 48 deubiquitinase 1 gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20160804 MGI 1558166 Mindy1 MINDY lysine 48 deubiquitinase 1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20141003 MGI 1558167 Prmt2 protein arginine N-methyltransferase 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16616919 1558167 Prmt2 protein arginine N-methyltransferase 2 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:16616919 1558167 Prmt2 protein arginine N-methyltransferase 2 gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20160804 MGI 1558168 Gins1 GINS complex subunit 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16287864 1558168 Gins1 GINS complex subunit 1 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:16287864 1558168 Gins1 GINS complex subunit 1 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:16287864 1558168 Gins1 GINS complex subunit 1 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16287864 1558168 Gins1 GINS complex subunit 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16287864 1558168 Gins1 GINS complex subunit 1 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:16287864 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0000610 cholestasis IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20210415 MGI PMID:32518166 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20210415 MGI PMID:32518166 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0008956 decreased cellular hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20210415 MGI PMID:32518166 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558169 Slc25a37 solute carrier family 25, member 37 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:21310927 1558172 Tspan18 tetraspanin 18 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220519 MGI 1558172 Tspan18 tetraspanin 18 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220519 MGI 1558172 Tspan18 tetraspanin 18 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20201022 MGI 1558172 Tspan18 tetraspanin 18 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 1558172 Tspan18 tetraspanin 18 gene MP:0009676 abnormal hemostasis IAGP N RGD:5509061 20210617 MGI PMID:30573509 1558172 Tspan18 tetraspanin 18 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1558172 Tspan18 tetraspanin 18 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20210617 MGI PMID:30573509 1558172 Tspan18 tetraspanin 18 gene MP:0031164 decreased circulating von Willebrand factor level IAGP N RGD:5509061 20210617 MGI PMID:30573509 1558178 Fbxo44 F-box protein 44 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1558178 Fbxo44 F-box protein 44 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1558178 Fbxo44 F-box protein 44 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1558179 Dusp9 dual specificity phosphatase 9 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:16135819 1558179 Dusp9 dual specificity phosphatase 9 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16135819 1558179 Dusp9 dual specificity phosphatase 9 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16135819 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:23100420 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:23100420 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:23100420 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:23100420 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16221497 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:23100420 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16221497 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:23100420 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:23100420 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20181227 MGI 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0008914 enlarged cerebellum IAGP N RGD:5509061 20141003 MGI PMID:23100420 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0009268 absent cerebellum fissure IAGP N RGD:5509061 20141003 MGI PMID:23100420 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0009964 abnormal cerebellum lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:23100420 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20141003 MGI PMID:23100420 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210520 MGI 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0010387 abnormal Bergmann glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23100420 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23100420 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16221497 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558180 Ric8a RIC8 guanine nucleotide exchange factor A gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1558182 Cenpa centromere protein A gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12906131 1558182 Cenpa centromere protein A gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:12906131 1558182 Cenpa centromere protein A gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12906131 1558182 Cenpa centromere protein A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12906131 1558182 Cenpa centromere protein A gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12906131 1558182 Cenpa centromere protein A gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12906131 1558182 Cenpa centromere protein A gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:12906131 1558182 Cenpa centromere protein A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:12906131 1558182 Cenpa centromere protein A gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:12906131 1558182 Cenpa centromere protein A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12906131 1558182 Cenpa centromere protein A gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:12906131 1558182 Cenpa centromere protein A gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:10655499 1558182 Cenpa centromere protein A gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:10655499 1558182 Cenpa centromere protein A gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10655499 1558182 Cenpa centromere protein A gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12906131 1558182 Cenpa centromere protein A gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10655499 1558182 Cenpa centromere protein A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12906131 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0000021 prominent ears IAGP N RGD:5509061 20171019 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220922 MGI 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20141003 MGI 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20160804 MGI 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20141003 MGI 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0002697 abnormal eye size IEA N RGD:5509061 20141003 MGI 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20171019 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20160804 MGI 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20141003 MGI 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20141003 MGI 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0004089 dilated sarcoplasmic reticulum IAGP N RGD:5509061 20141003 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20141003 MGI 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20141003 MGI 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0005586 decreased tidal volume IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20141003 MGI 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20141003 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:19451219 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20190711 MGI PMID:22343142 1558185 Cisd2 CDGSH iron sulfur domain 2 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:19451219 1558188 Tmem43 transmembrane protein 43 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20141003 MGI 1558188 Tmem43 transmembrane protein 43 gene MP:0004300 abnormal organ of Corti supporting cell morphology IAGP N RGD:5509061 20220331 MGI PMID:34050020 1558188 Tmem43 transmembrane protein 43 gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20220331 MGI PMID:34050020 1558188 Tmem43 transmembrane protein 43 gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20220331 MGI PMID:34050020 1558188 Tmem43 transmembrane protein 43 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20220331 MGI PMID:34050020 1558188 Tmem43 transmembrane protein 43 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20220331 MGI PMID:34050020 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0002883 chromatolysis IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0009718 absent Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558190 Cdk5r2 cyclin dependent kinase 5, regulatory subunit 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11517264 1558191 Hunk hormonally upregulated Neu-associated kinase gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:19717424 1558191 Hunk hormonally upregulated Neu-associated kinase gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20201022 MGI 1558191 Hunk hormonally upregulated Neu-associated kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19717424 1558191 Hunk hormonally upregulated Neu-associated kinase gene MP:0002626 increased heart rate IEA N RGD:5509061 20210128 MGI 1558191 Hunk hormonally upregulated Neu-associated kinase gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20211021 MGI 1558191 Hunk hormonally upregulated Neu-associated kinase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1558192 Itsn2 intersectin 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1558192 Itsn2 intersectin 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1558192 Itsn2 intersectin 2 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20150430 MGI 1558192 Itsn2 intersectin 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:23447614 1558192 Itsn2 intersectin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23447614 1558192 Itsn2 intersectin 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1558192 Itsn2 intersectin 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23447614 1558192 Itsn2 intersectin 2 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20201022 MGI 1558192 Itsn2 intersectin 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:23447614 1558192 Itsn2 intersectin 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20180802 MGI PMID:29773874 1558192 Itsn2 intersectin 2 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:23447614 1558192 Itsn2 intersectin 2 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20180802 MGI PMID:29773874 1558192 Itsn2 intersectin 2 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23447614 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0012220 abnormal ether lipid level IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558194 Far1 fatty acyl CoA reductase 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20230921 MGI PMID:37039784 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17937813 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17937813 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23024777 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240314 MGI PMID:34901307 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001263 weight loss IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23024777 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:14555645 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:17937813 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:14555645 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20240314 MGI PMID:34901307 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23024777 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:14555645 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17937813 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0002083 premature death IAGP N RGD:5509061 20240314 MGI PMID:34901307 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17937813 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0002176 increased brain weight IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23024777 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0003017 decreased circulating bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0003030 acidemia IAGP N RGD:5509061 20141003 MGI PMID:17937813 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0003031 acidosis IAGP N RGD:5509061 20141003 MGI PMID:23024777 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0003031 acidosis IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0003620 oliguria IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:23024777 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20141003 MGI PMID:14555645 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20141003 MGI PMID:23024777 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20160804 MGI PMID:23024777 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:14555645 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:14555645 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17937813 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0010028 aciduria IAGP N RGD:5509061 20141003 MGI PMID:17937813 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20141003 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17937813 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20240314 MGI PMID:34901307 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14555645 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23024777 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20180906 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0011435 increased urine magnesium level IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0011637 abnormal mitochondrial matrix morphology IAGP N RGD:5509061 20141003 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0012230 abnormal sphingolipid level IAGP N RGD:5509061 20180531 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20141003 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0030612 organic aciduria IAGP N RGD:5509061 20180906 MGI PMID:19088183 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0030614 methylmalonic aciduria IAGP N RGD:5509061 20180906 MGI PMID:14555645 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0030614 methylmalonic aciduria IAGP N RGD:5509061 20180906 MGI PMID:23024777 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0030614 methylmalonic aciduria IAGP N RGD:5509061 20180906 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0030630 increased circulating methylmalonic acid level IAGP N RGD:5509061 20220120 MGI PMID:23898205 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0030630 increased circulating methylmalonic acid level IAGP N RGD:5509061 20240314 MGI PMID:34901307 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0030655 increased circulating glycine level IAGP N RGD:5509061 20180913 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0031339 increased lipocalin 2 level IAGP N RGD:5509061 20220120 MGI PMID:27519416 1558195 Mmut methylmalonyl-Coenzyme A mutase gene MP:0031342 increased circulating lipocalin 2 level IAGP N RGD:5509061 20220120 MGI PMID:23898205 1558196 Slc29a4 solute carrier family 29 (nucleoside transporters), member 4 gene MP:0000552 abnormal radius morphology IEA N RGD:5509061 20200514 MGI 1558196 Slc29a4 solute carrier family 29 (nucleoside transporters), member 4 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:23255610 1558196 Slc29a4 solute carrier family 29 (nucleoside transporters), member 4 gene MP:0005108 abnormal ulna morphology IEA N RGD:5509061 20200514 MGI 1558197 Cabp2 calcium binding protein 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220811 MGI 1558197 Cabp2 calcium binding protein 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1558197 Cabp2 calcium binding protein 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1558197 Cabp2 calcium binding protein 2 gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20180524 MGI PMID:28183797 1558197 Cabp2 calcium binding protein 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1558197 Cabp2 calcium binding protein 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20180531 MGI PMID:27822497 1558197 Cabp2 calcium binding protein 2 gene MP:0006335 abnormal hearing electrophysiology IAGP N RGD:5509061 20180524 MGI PMID:28183797 1558197 Cabp2 calcium binding protein 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1558197 Cabp2 calcium binding protein 2 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20180524 MGI PMID:28183797 1558197 Cabp2 calcium binding protein 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20180524 MGI PMID:28183797 1558198 Edaradd EDAR associated via death domain gene MP:0000017 big ears IEA N RGD:5509061 20111116 MGI 1558198 Edaradd EDAR associated via death domain gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:1166079 1558198 Edaradd EDAR associated via death domain gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:1166079 1558198 Edaradd EDAR associated via death domain gene MP:0000416 sparse hair IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0000417 short hair IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:5893447 1558198 Edaradd EDAR associated via death domain gene MP:0000418 focal hair loss IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:5893447 1558198 Edaradd EDAR associated via death domain gene MP:0000585 kinked tail IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:896803 1558198 Edaradd EDAR associated via death domain gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:896803 1558198 Edaradd EDAR associated via death domain gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:896803 1558198 Edaradd EDAR associated via death domain gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:133823 1558198 Edaradd EDAR associated via death domain gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:133823 1558198 Edaradd EDAR associated via death domain gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:896803 1558198 Edaradd EDAR associated via death domain gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:1166079 1558198 Edaradd EDAR associated via death domain gene MP:0001199 thin skin IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:1166079 1558198 Edaradd EDAR associated via death domain gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1558198 Edaradd EDAR associated via death domain gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0001314 cornea opacity IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0001340 abnormal eyelid morphology IEA N RGD:5509061 20111116 MGI 1558198 Edaradd EDAR associated via death domain gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20111116 MGI 1558198 Edaradd EDAR associated via death domain gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:896803 1558198 Edaradd EDAR associated via death domain gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:133823 1558198 Edaradd EDAR associated via death domain gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:896803 1558198 Edaradd EDAR associated via death domain gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0001950 abnormal respiratory sounds IEA N RGD:5509061 20111116 MGI 1558198 Edaradd EDAR associated via death domain gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:320066 1558198 Edaradd EDAR associated via death domain gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1166079 1558198 Edaradd EDAR associated via death domain gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:1166079 1558198 Edaradd EDAR associated via death domain gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:133823 1558198 Edaradd EDAR associated via death domain gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0002083 premature death IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:5893447 1558198 Edaradd EDAR associated via death domain gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20111116 MGI 1558198 Edaradd EDAR associated via death domain gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:896803 1558198 Edaradd EDAR associated via death domain gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0002277 abnormal respiratory mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:15973734 1558198 Edaradd EDAR associated via death domain gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:5893447 1558198 Edaradd EDAR associated via death domain gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:896803 1558198 Edaradd EDAR associated via death domain gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:133823 1558198 Edaradd EDAR associated via death domain gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:133823 1558198 Edaradd EDAR associated via death domain gene MP:0003932 abnormal molar crown morphology IAGP N RGD:5509061 20180125 MGI PMID:478295 1558198 Edaradd EDAR associated via death domain gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:5893447 1558198 Edaradd EDAR associated via death domain gene MP:0006236 absent Meibomian glands IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0006365 absent guard hair IAGP N RGD:5509061 20141003 MGI PMID:5893447 1558198 Edaradd EDAR associated via death domain gene MP:0006365 absent guard hair IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0006366 absent zigzag hairs IAGP N RGD:5509061 20141003 MGI PMID:5893447 1558198 Edaradd EDAR associated via death domain gene MP:0006366 absent zigzag hairs IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0006400 decreased molar number IAGP N RGD:5509061 20141003 MGI PMID:5893447 1558198 Edaradd EDAR associated via death domain gene MP:0006402 small molars IAGP N RGD:5509061 20141003 MGI PMID:478295 1558198 Edaradd EDAR associated via death domain gene MP:0006402 small molars IAGP N RGD:5509061 20141003 MGI PMID:5893447 1558198 Edaradd EDAR associated via death domain gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20141003 MGI PMID:896803 1558198 Edaradd EDAR associated via death domain gene MP:0009825 cornea ulcer IEA N RGD:5509061 20160310 MGI 1558198 Edaradd EDAR associated via death domain gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20141003 MGI PMID:896803 1558198 Edaradd EDAR associated via death domain gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230119 MGI 1558198 Edaradd EDAR associated via death domain gene MP:0012078 abnormal tail ring morphology IEA N RGD:5509061 20170309 MGI 1558198 Edaradd EDAR associated via death domain gene MP:0013176 abnormal tail position or orientation IEA N RGD:5509061 20141003 MGI 1558198 Edaradd EDAR associated via death domain gene MP:0013897 decreased eyelid cilium number IAGP N RGD:5509061 20200123 MGI PMID:24539712 1558198 Edaradd EDAR associated via death domain gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20171221 MGI PMID:5893447 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20190103 MGI PMID:27518564 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20231207 MGI 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20190103 MGI PMID:27518564 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20190103 MGI PMID:27518564 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20190103 MGI PMID:27518564 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20190103 MGI PMID:27518564 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20231207 MGI 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20190103 MGI PMID:27518564 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20190103 MGI PMID:27518564 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20190103 MGI PMID:27518564 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20190103 MGI PMID:27518564 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20190103 MGI PMID:27518564 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20190103 MGI PMID:27518564 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20190103 MGI PMID:27518564 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0013694 abnormal granulocyte monocyte progenitor cell morphology IAGP N RGD:5509061 20190103 MGI PMID:27518564 1558200 Ang angiogenin, ribonuclease, RNase A family, 5 gene MP:0013702 abnormal megakaryocyte-erythroid progenitor cell morphology IAGP N RGD:5509061 20190103 MGI PMID:27518564 1558202 Tmem114 transmembrane protein 114 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201022 MGI PMID:32588039 1558203 Zfp827 zinc finger protein 827 gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1558203 Zfp827 zinc finger protein 827 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1558203 Zfp827 zinc finger protein 827 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1558203 Zfp827 zinc finger protein 827 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558207 Cdk17 cyclin dependent kinase 17 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20240523 MGI 1558207 Cdk17 cyclin dependent kinase 17 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1558207 Cdk17 cyclin dependent kinase 17 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1558207 Cdk17 cyclin dependent kinase 17 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1558207 Cdk17 cyclin dependent kinase 17 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558208 Cd209d CD209d antigen gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:19770268 1558208 Cd209d CD209d antigen gene MP:0005014 increased B cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1558208 Cd209d CD209d antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20150226 MGI PMID:23118208 1558208 Cd209d CD209d antigen gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19770268 1558208 Cd209d CD209d antigen gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20150226 MGI PMID:23118208 1558212 Ahctf1 AT hook containing transcription factor 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20210520 MGI 1558212 Ahctf1 AT hook containing transcription factor 1 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:15507119 1558212 Ahctf1 AT hook containing transcription factor 1 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15507119 1558212 Ahctf1 AT hook containing transcription factor 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15507119 1558212 Ahctf1 AT hook containing transcription factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558212 Ahctf1 AT hook containing transcription factor 1 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:15507119 1558214 Rspo3 R-spondin 3 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20150716 MGI PMID:25053429 1558214 Rspo3 R-spondin 3 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20150129 MGI PMID:18842812 1558214 Rspo3 R-spondin 3 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20150716 MGI PMID:25053429 1558214 Rspo3 R-spondin 3 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0000561 adactyly IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16963017 1558214 Rspo3 R-spondin 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20150129 MGI PMID:18842812 1558214 Rspo3 R-spondin 3 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:16963017 1558214 Rspo3 R-spondin 3 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20150129 MGI PMID:18842812 1558214 Rspo3 R-spondin 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16963017 1558214 Rspo3 R-spondin 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20150129 MGI PMID:18842812 1558214 Rspo3 R-spondin 3 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20150716 MGI PMID:25053429 1558214 Rspo3 R-spondin 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20150129 MGI PMID:18842812 1558214 Rspo3 R-spondin 3 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20150716 MGI PMID:25053429 1558214 Rspo3 R-spondin 3 gene MP:0002728 absent tibia IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20150129 MGI PMID:18842812 1558214 Rspo3 R-spondin 3 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20150716 MGI PMID:25053429 1558214 Rspo3 R-spondin 3 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20150716 MGI PMID:25053429 1558214 Rspo3 R-spondin 3 gene MP:0004371 bowed femur IAGP N RGD:5509061 20181011 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20150716 MGI PMID:25053429 1558214 Rspo3 R-spondin 3 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16963017 1558214 Rspo3 R-spondin 3 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16963017 1558214 Rspo3 R-spondin 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22610508 1558214 Rspo3 R-spondin 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20150716 MGI PMID:25053429 1558214 Rspo3 R-spondin 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20150716 MGI PMID:25053429 1558215 Nptx2 neuronal pentraxin 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:16763034 1558215 Nptx2 neuronal pentraxin 2 gene MP:0002802 abnormal discrimination learning IAGP N RGD:5509061 20141003 MGI PMID:18057201 1558215 Nptx2 neuronal pentraxin 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16763034 1558216 Dach2 dachshund family transcription factor 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1558216 Dach2 dachshund family transcription factor 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1558216 Dach2 dachshund family transcription factor 2 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20230601 MGI 1558216 Dach2 dachshund family transcription factor 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1558216 Dach2 dachshund family transcription factor 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1558216 Dach2 dachshund family transcription factor 2 gene MP:0000692 small spleen IEA N RGD:5509061 20230601 MGI 1558216 Dach2 dachshund family transcription factor 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1558216 Dach2 dachshund family transcription factor 2 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20230601 MGI 1558216 Dach2 dachshund family transcription factor 2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1558216 Dach2 dachshund family transcription factor 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1558216 Dach2 dachshund family transcription factor 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1558216 Dach2 dachshund family transcription factor 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1558216 Dach2 dachshund family transcription factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16470613 1558216 Dach2 dachshund family transcription factor 2 gene MP:0002217 small lymph nodes IEA N RGD:5509061 20230601 MGI 1558216 Dach2 dachshund family transcription factor 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1558216 Dach2 dachshund family transcription factor 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20230601 MGI 1558216 Dach2 dachshund family transcription factor 2 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20230601 MGI 1558220 Siglece sialic acid binding Ig-like lectin E gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20180913 MGI PMID:28100677 1558220 Siglece sialic acid binding Ig-like lectin E gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:23315163 1558220 Siglece sialic acid binding Ig-like lectin E gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:23315163 1558220 Siglece sialic acid binding Ig-like lectin E gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20180913 MGI PMID:28100677 1558220 Siglece sialic acid binding Ig-like lectin E gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20180913 MGI PMID:28100677 1558220 Siglece sialic acid binding Ig-like lectin E gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20180913 MGI PMID:28100677 1558222 Kcnk5 potassium channel, subfamily K, member 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15141089 1558222 Kcnk5 potassium channel, subfamily K, member 5 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:20133877 1558222 Kcnk5 potassium channel, subfamily K, member 5 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:20133877 1558222 Kcnk5 potassium channel, subfamily K, member 5 gene MP:0005556 abnormal renal filtration rate IAGP N RGD:5509061 20141003 MGI PMID:15141089 1558222 Kcnk5 potassium channel, subfamily K, member 5 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:15141089 1558222 Kcnk5 potassium channel, subfamily K, member 5 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12707131 1558222 Kcnk5 potassium channel, subfamily K, member 5 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15141089 1558222 Kcnk5 potassium channel, subfamily K, member 5 gene MP:0011406 abnormal retrotrapezoid nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:20133877 1558222 Kcnk5 potassium channel, subfamily K, member 5 gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:15141089 1558226 Jdp2 Jun dimerization protein 2 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23200825 1558226 Jdp2 Jun dimerization protein 2 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:23200825 1558226 Jdp2 Jun dimerization protein 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23200825 1558226 Jdp2 Jun dimerization protein 2 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20802531 1558226 Jdp2 Jun dimerization protein 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:20802531 1558226 Jdp2 Jun dimerization protein 2 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:20802531 1558226 Jdp2 Jun dimerization protein 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1558226 Jdp2 Jun dimerization protein 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23200825 1558226 Jdp2 Jun dimerization protein 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:23200825 1558226 Jdp2 Jun dimerization protein 2 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:20802531 1558226 Jdp2 Jun dimerization protein 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:20802531 1558226 Jdp2 Jun dimerization protein 2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:23200825 1558226 Jdp2 Jun dimerization protein 2 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:23200825 1558226 Jdp2 Jun dimerization protein 2 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:23200825 1558226 Jdp2 Jun dimerization protein 2 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17464331 1558226 Jdp2 Jun dimerization protein 2 gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:23200825 1558226 Jdp2 Jun dimerization protein 2 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:20802531 1558226 Jdp2 Jun dimerization protein 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:23200825 1558226 Jdp2 Jun dimerization protein 2 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17464331 1558226 Jdp2 Jun dimerization protein 2 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23200825 1558226 Jdp2 Jun dimerization protein 2 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:23200825 1558227 Acot5 acyl-CoA thioesterase 5 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1558227 Acot5 acyl-CoA thioesterase 5 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1558228 Cep70 centrosomal protein 70 gene MP:0001147 small testis IAGP N RGD:5509061 20230316 MGI PMID:33980814 1558228 Cep70 centrosomal protein 70 gene MP:0001925 male infertility IAGP N RGD:5509061 20230316 MGI PMID:33980814 1558228 Cep70 centrosomal protein 70 gene MP:0001926 female infertility IEA N RGD:5509061 20240523 MGI 1558228 Cep70 centrosomal protein 70 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230316 MGI PMID:33980814 1558228 Cep70 centrosomal protein 70 gene MP:0005159 azoospermia IAGP N RGD:5509061 20230316 MGI PMID:33980814 1558228 Cep70 centrosomal protein 70 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230316 MGI PMID:33980814 1558228 Cep70 centrosomal protein 70 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20230316 MGI PMID:33980814 1558228 Cep70 centrosomal protein 70 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20230316 MGI PMID:33980814 1558228 Cep70 centrosomal protein 70 gene MP:0009235 small sperm head IAGP N RGD:5509061 20230316 MGI PMID:33980814 1558228 Cep70 centrosomal protein 70 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20230316 MGI PMID:33980814 1558228 Cep70 centrosomal protein 70 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20230316 MGI PMID:33980814 1558228 Cep70 centrosomal protein 70 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20230316 MGI PMID:33980814 1558228 Cep70 centrosomal protein 70 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20230316 MGI PMID:33980814 1558230 Bbln bublin coiled coil protein gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20201210 MGI PMID:32569872 1558230 Bbln bublin coiled coil protein gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20201210 MGI PMID:32569872 1558230 Bbln bublin coiled coil protein gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20201210 MGI PMID:32569872 1558230 Bbln bublin coiled coil protein gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20201210 MGI PMID:32569872 1558230 Bbln bublin coiled coil protein gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20201231 MGI PMID:32569872 1558230 Bbln bublin coiled coil protein gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20201231 MGI PMID:32569872 1558230 Bbln bublin coiled coil protein gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20201231 MGI PMID:32569872 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:9817932 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:14625552 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9817932 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:9817932 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9817932 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14625552 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:9817932 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:9817932 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0009420 skeletal muscle endomysial fibrosis IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558231 Col6a1 collagen, type VI, alpha 1 gene MP:0010240 decreased skeletal muscle size IAGP N RGD:5509061 20200409 MGI PMID:28043812 1558232 Rp2 retinitis pigmentosa 2 homolog gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20150402 MGI PMID:23745007 1558232 Rp2 retinitis pigmentosa 2 homolog gene MP:0002090 abnormal vision IAGP N RGD:5509061 20180222 MGI PMID:25422369 1558232 Rp2 retinitis pigmentosa 2 homolog gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20150402 MGI PMID:23745007 1558232 Rp2 retinitis pigmentosa 2 homolog gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20150402 MGI PMID:23745007 1558232 Rp2 retinitis pigmentosa 2 homolog gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20180222 MGI PMID:25422369 1558232 Rp2 retinitis pigmentosa 2 homolog gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20150402 MGI PMID:23745007 1558232 Rp2 retinitis pigmentosa 2 homolog gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20150402 MGI PMID:23745007 1558232 Rp2 retinitis pigmentosa 2 homolog gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20150402 MGI PMID:23745007 1558232 Rp2 retinitis pigmentosa 2 homolog gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20180222 MGI PMID:25422369 1558232 Rp2 retinitis pigmentosa 2 homolog gene MP:0012031 abnormal b-wave amplitude IAGP N RGD:5509061 20180222 MGI PMID:25422369 1558232 Rp2 retinitis pigmentosa 2 homolog gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20180222 MGI PMID:23745007 1558232 Rp2 retinitis pigmentosa 2 homolog gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20180222 MGI PMID:25422369 1558232 Rp2 retinitis pigmentosa 2 homolog gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20180222 MGI PMID:23745007 1558232 Rp2 retinitis pigmentosa 2 homolog gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20180222 MGI PMID:25422369 1558232 Rp2 retinitis pigmentosa 2 homolog gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:25422369 1558236 Coro2b coronin, actin binding protein, 2B gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1558236 Coro2b coronin, actin binding protein, 2B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20191219 MGI PMID:31221975 1558236 Coro2b coronin, actin binding protein, 2B gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20180329 MGI PMID:29162887 1558236 Coro2b coronin, actin binding protein, 2B gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20191219 MGI PMID:31221975 1558236 Coro2b coronin, actin binding protein, 2B gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20180329 MGI PMID:29162887 1558236 Coro2b coronin, actin binding protein, 2B gene MP:0006315 abnormal urine protein level IAGP N RGD:5509061 20180329 MGI PMID:29162887 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0002626 increased heart rate IEA N RGD:5509061 20240523 MGI 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0009710 anhedonia IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0010507 shortened RR interval IEA N RGD:5509061 20240523 MGI 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0011749 perivascular fibrosis IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0020396 abnormal social recognition IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558237 Cmya5 cardiomyopathy associated 5 gene MP:0020874 abnormal nervous system dopamine level IAGP N RGD:5509061 20220428 MGI PMID:34037836 1558238 Mef2b myocyte enhancer factor 2B gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20210128 MGI 1558238 Mef2b myocyte enhancer factor 2B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200409 MGI PMID:30205047 1558238 Mef2b myocyte enhancer factor 2B gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200409 MGI PMID:30205047 1558238 Mef2b myocyte enhancer factor 2B gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20200409 MGI PMID:30205047 1558238 Mef2b myocyte enhancer factor 2B gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20200409 MGI PMID:30205047 1558238 Mef2b myocyte enhancer factor 2B gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20200409 MGI PMID:30205047 1558238 Mef2b myocyte enhancer factor 2B gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20200409 MGI PMID:30205047 1558238 Mef2b myocyte enhancer factor 2B gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20200409 MGI PMID:30205047 1558238 Mef2b myocyte enhancer factor 2B gene MP:0009317 increased follicular lymphoma incidence IAGP N RGD:5509061 20200409 MGI PMID:30205047 1558238 Mef2b myocyte enhancer factor 2B gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20200409 MGI PMID:30205047 1558239 Wrap53 WD repeat containing, antisense to Trp53 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20201022 MGI 1558239 Wrap53 WD repeat containing, antisense to Trp53 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20201022 MGI 1558239 Wrap53 WD repeat containing, antisense to Trp53 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1558239 Wrap53 WD repeat containing, antisense to Trp53 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1558239 Wrap53 WD repeat containing, antisense to Trp53 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1558239 Wrap53 WD repeat containing, antisense to Trp53 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 1558239 Wrap53 WD repeat containing, antisense to Trp53 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1558239 Wrap53 WD repeat containing, antisense to Trp53 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1558239 Wrap53 WD repeat containing, antisense to Trp53 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20181227 MGI 1558239 Wrap53 WD repeat containing, antisense to Trp53 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1558239 Wrap53 WD repeat containing, antisense to Trp53 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558239 Wrap53 WD repeat containing, antisense to Trp53 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1558244 Ccdc18 coiled-coil domain containing 18 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20181227 MGI 1558244 Ccdc18 coiled-coil domain containing 18 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20210128 MGI 1558244 Ccdc18 coiled-coil domain containing 18 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1558244 Ccdc18 coiled-coil domain containing 18 gene MP:0003443 increased circulating glycerol level IEA N RGD:5509061 20211021 MGI 1558244 Ccdc18 coiled-coil domain containing 18 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 1558244 Ccdc18 coiled-coil domain containing 18 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1558245 Irf3 interferon regulatory factor 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1558245 Irf3 interferon regulatory factor 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1558245 Irf3 interferon regulatory factor 3 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200130 MGI PMID:31281243 1558245 Irf3 interferon regulatory factor 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1558245 Irf3 interferon regulatory factor 3 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20231207 MGI 1558245 Irf3 interferon regulatory factor 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20190523 MGI PMID:28951494 1558245 Irf3 interferon regulatory factor 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1558245 Irf3 interferon regulatory factor 3 gene MP:0002188 small heart IEA N RGD:5509061 20201022 MGI 1558245 Irf3 interferon regulatory factor 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20351692 1558245 Irf3 interferon regulatory factor 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1558245 Irf3 interferon regulatory factor 3 gene MP:0002989 small kidney IEA N RGD:5509061 20201022 MGI 1558245 Irf3 interferon regulatory factor 3 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11070172 1558245 Irf3 interferon regulatory factor 3 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20200130 MGI PMID:31281243 1558245 Irf3 interferon regulatory factor 3 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20200130 MGI PMID:31281243 1558245 Irf3 interferon regulatory factor 3 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20190523 MGI PMID:28951494 1558245 Irf3 interferon regulatory factor 3 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20150212 MGI PMID:19617565 1558245 Irf3 interferon regulatory factor 3 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200130 MGI PMID:31281243 1558245 Irf3 interferon regulatory factor 3 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200130 MGI PMID:31281243 1558245 Irf3 interferon regulatory factor 3 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20200130 MGI PMID:31281243 1558245 Irf3 interferon regulatory factor 3 gene MP:0008548 abnormal circulating interferon level IAGP N RGD:5509061 20141003 MGI PMID:11070172 1558245 Irf3 interferon regulatory factor 3 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20351692 1558245 Irf3 interferon regulatory factor 3 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20351692 1558245 Irf3 interferon regulatory factor 3 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200130 MGI PMID:31281243 1558245 Irf3 interferon regulatory factor 3 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200130 MGI PMID:31281243 1558245 Irf3 interferon regulatory factor 3 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200130 MGI PMID:31281243 1558245 Irf3 interferon regulatory factor 3 gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20190523 MGI PMID:28951494 1558245 Irf3 interferon regulatory factor 3 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:20351692 1558245 Irf3 interferon regulatory factor 3 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:11070172 1558245 Irf3 interferon regulatory factor 3 gene MP:0020952 increased susceptibility to Paramyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:20351692 1558246 Sertad1 SERTA domain containing 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20090907 1558246 Sertad1 SERTA domain containing 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20090907 1558246 Sertad1 SERTA domain containing 1 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:20090907 1558246 Sertad1 SERTA domain containing 1 gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:20090907 1558247 Bank1 B cell scaffold protein with ankyrin repeats 1 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:16546095 1558247 Bank1 B cell scaffold protein with ankyrin repeats 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16546095 1558247 Bank1 B cell scaffold protein with ankyrin repeats 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16546095 1558247 Bank1 B cell scaffold protein with ankyrin repeats 1 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16546095 1558247 Bank1 B cell scaffold protein with ankyrin repeats 1 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16546095 1558247 Bank1 B cell scaffold protein with ankyrin repeats 1 gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:16546095 1558247 Bank1 B cell scaffold protein with ankyrin repeats 1 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16546095 1558247 Bank1 B cell scaffold protein with ankyrin repeats 1 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:16546095 1558247 Bank1 B cell scaffold protein with ankyrin repeats 1 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:16546095 1558247 Bank1 B cell scaffold protein with ankyrin repeats 1 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16546095 1558247 Bank1 B cell scaffold protein with ankyrin repeats 1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16546095 1558248 Gas2 growth arrest specific 2 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20180719 MGI PMID:27734842 1558248 Gas2 growth arrest specific 2 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20180719 MGI PMID:27734842 1558248 Gas2 growth arrest specific 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20180719 MGI PMID:27734842 1558248 Gas2 growth arrest specific 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20180719 MGI PMID:27734842 1558248 Gas2 growth arrest specific 2 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20220616 MGI PMID:33964205 1558248 Gas2 growth arrest specific 2 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20180719 MGI PMID:27734842 1558248 Gas2 growth arrest specific 2 gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20180719 MGI PMID:27734842 1558248 Gas2 growth arrest specific 2 gene MP:0003582 abnormal ovary development IAGP N RGD:5509061 20180719 MGI PMID:27734842 1558248 Gas2 growth arrest specific 2 gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20220616 MGI PMID:33964205 1558248 Gas2 growth arrest specific 2 gene MP:0004273 abnormal basal lamina morphology IAGP N RGD:5509061 20180719 MGI PMID:27734842 1558248 Gas2 growth arrest specific 2 gene MP:0004300 abnormal organ of Corti supporting cell morphology IAGP N RGD:5509061 20220616 MGI PMID:33964205 1558248 Gas2 growth arrest specific 2 gene MP:0004302 abnormal Deiters cell morphology IAGP N RGD:5509061 20220616 MGI PMID:33964205 1558248 Gas2 growth arrest specific 2 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20220616 MGI PMID:33964205 1558248 Gas2 growth arrest specific 2 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20220616 MGI PMID:33964205 1558248 Gas2 growth arrest specific 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20220616 MGI PMID:33964205 1558248 Gas2 growth arrest specific 2 gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20180719 MGI PMID:27734842 1558248 Gas2 growth arrest specific 2 gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20180719 MGI PMID:27734842 1558248 Gas2 growth arrest specific 2 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20180719 MGI PMID:27734842 1558248 Gas2 growth arrest specific 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20220616 MGI PMID:33964205 1558249 Phldb2 pleckstrin homology like domain, family B, member 2 gene MP:0001333 absent optic nerve IEA N RGD:5509061 20200402 MGI 1558249 Phldb2 pleckstrin homology like domain, family B, member 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20191107 MGI PMID:30867511 1558249 Phldb2 pleckstrin homology like domain, family B, member 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 1558249 Phldb2 pleckstrin homology like domain, family B, member 2 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1558249 Phldb2 pleckstrin homology like domain, family B, member 2 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20191107 MGI PMID:30867511 1558249 Phldb2 pleckstrin homology like domain, family B, member 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20191107 MGI PMID:30867511 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20191114 MGI PMID:28747345 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0000692 small spleen IAGP N RGD:5509061 20191114 MGI PMID:28747345 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240627 MGI PMID:37316542 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0001265 decreased body size IAGP N RGD:5509061 20240627 MGI PMID:37316542 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20230202 MGI PMID:33643282 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20240627 MGI PMID:37316542 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0002531 abnormal type I hypersensitivity reaction IAGP N RGD:5509061 20230202 MGI PMID:33643282 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20230202 MGI PMID:33643282 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20230202 MGI PMID:33643282 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20230202 MGI PMID:33643282 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20230202 MGI PMID:33643282 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20191114 MGI PMID:28747345 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240627 MGI PMID:37316542 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0020116 increased sphingosine level IAGP N RGD:5509061 20230202 MGI PMID:33643282 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0020116 increased sphingosine level IAGP N RGD:5509061 20240627 MGI PMID:37316542 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0020582 increased ceramide level IAGP N RGD:5509061 20230202 MGI PMID:33643282 1558251 Ormdl3 ORM1-like 3 (S. cerevisiae) gene MP:0020582 increased ceramide level IAGP N RGD:5509061 20240627 MGI PMID:37316542 1558254 Lonrf2 LON peptidase N-terminal domain and ring finger 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20220519 MGI 1558254 Lonrf2 LON peptidase N-terminal domain and ring finger 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220811 MGI 1558254 Lonrf2 LON peptidase N-terminal domain and ring finger 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220519 MGI 1558254 Lonrf2 LON peptidase N-terminal domain and ring finger 2 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210826 MGI 1558254 Lonrf2 LON peptidase N-terminal domain and ring finger 2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20240523 MGI 1558254 Lonrf2 LON peptidase N-terminal domain and ring finger 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1558256 Cldnd2 claudin domain containing 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 1558256 Cldnd2 claudin domain containing 2 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1558256 Cldnd2 claudin domain containing 2 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20211021 MGI 1558256 Cldnd2 claudin domain containing 2 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 1558256 Cldnd2 claudin domain containing 2 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20210128 MGI 1558256 Cldnd2 claudin domain containing 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20200402 MGI PMID:31978606 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20200310 MGI PMID:31439632 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20200310 MGI PMID:31439632 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200402 MGI PMID:31978606 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20200310 MGI PMID:31439632 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200402 MGI PMID:31978606 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200402 MGI PMID:31978606 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20200402 MGI PMID:30842726 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20200310 MGI PMID:31439632 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20200402 MGI PMID:31978606 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20200402 MGI PMID:31978606 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20200402 MGI PMID:30842726 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200402 MGI PMID:31978606 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20200402 MGI PMID:31978606 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20200402 MGI PMID:31978606 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20200310 MGI PMID:31439632 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20200310 MGI PMID:31439632 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:31439632 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0011987 abnormal GABAergic neuron physiology IAGP N RGD:5509061 20200402 MGI PMID:31978606 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200310 MGI PMID:31439632 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200402 MGI PMID:30842726 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0012348 decreased susceptibility to induction of seizure by inducing agent IAGP N RGD:5509061 20200402 MGI PMID:31978606 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0012459 increased dentate gyrus size IAGP N RGD:5509061 20200310 MGI PMID:31439632 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0020082 increased hippocampus volume IAGP N RGD:5509061 20200310 MGI PMID:31439632 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20200402 MGI PMID:31978606 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20200402 MGI PMID:30842726 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0020573 abnormal corpus callosum size IAGP N RGD:5509061 20200310 MGI PMID:31439632 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:30842726 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:31439632 1558257 Iqsec2 IQ motif and Sec7 domain 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:31978606 1558258 Nap1l2 nucleosome assembly protein 1-like 2 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20141003 MGI 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20221215 MGI 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0001304 cataract IEA N RGD:5509061 20210128 MGI 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:20577052 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:20577052 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:20634410 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0001513 limb grasping IEA N RGD:5509061 20210128 MGI 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0001522 impaired swimming IAGP N RGD:5509061 20200310 MGI PMID:20577052 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20200514 MGI 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200310 MGI PMID:20577052 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0002764 short tibia IEA N RGD:5509061 20220519 MGI 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20200310 MGI PMID:20634410 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20200310 MGI PMID:20577052 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220519 MGI 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200514 MGI 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0002978 absent otoliths IAGP N RGD:5509061 20200310 MGI PMID:20577052 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0003143 enlarged otoliths IAGP N RGD:5509061 20200310 MGI PMID:20577052 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220519 MGI 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0004330 abnormal vestibular saccular macula morphology IAGP N RGD:5509061 20200310 MGI PMID:20577052 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20221215 MGI 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0005191 head tilt IAGP N RGD:5509061 20200310 MGI PMID:20577052 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20221215 MGI 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20200310 MGI PMID:20577052 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0009979 abnormal cerebellum deep nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:20634410 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20634410 1558262 Atg4b autophagy related 4B, cysteine peptidase gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200310 MGI PMID:20577052 1558263 Tpk1 thiamine pyrophosphokinase gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1558263 Tpk1 thiamine pyrophosphokinase gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1558263 Tpk1 thiamine pyrophosphokinase gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191128 MGI 1558263 Tpk1 thiamine pyrophosphokinase gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191128 MGI 1558263 Tpk1 thiamine pyrophosphokinase gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191128 MGI 1558263 Tpk1 thiamine pyrophosphokinase gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1558263 Tpk1 thiamine pyrophosphokinase gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191128 MGI 1558263 Tpk1 thiamine pyrophosphokinase gene MP:0009331 absent primitive node IEA N RGD:5509061 20191128 MGI 1558263 Tpk1 thiamine pyrophosphokinase gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1558263 Tpk1 thiamine pyrophosphokinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558263 Tpk1 thiamine pyrophosphokinase gene MP:0012724 absent head fold IEA N RGD:5509061 20191128 MGI 1558263 Tpk1 thiamine pyrophosphokinase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20190502 MGI 1558265 Inpp5k inositol polyphosphate 5-phosphatase K gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20201022 MGI 1558265 Inpp5k inositol polyphosphate 5-phosphatase K gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18573875 1558265 Inpp5k inositol polyphosphate 5-phosphatase K gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18573875 1558265 Inpp5k inositol polyphosphate 5-phosphatase K gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18573875 1558265 Inpp5k inositol polyphosphate 5-phosphatase K gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:18573875 1558265 Inpp5k inositol polyphosphate 5-phosphatase K gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18573875 1558265 Inpp5k inositol polyphosphate 5-phosphatase K gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:18573875 1558265 Inpp5k inositol polyphosphate 5-phosphatase K gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18573875 1558265 Inpp5k inositol polyphosphate 5-phosphatase K gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18573875 1558265 Inpp5k inositol polyphosphate 5-phosphatase K gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:18573875 1558265 Inpp5k inositol polyphosphate 5-phosphatase K gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18573875 1558265 Inpp5k inositol polyphosphate 5-phosphatase K gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18573875 1558265 Inpp5k inositol polyphosphate 5-phosphatase K gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18573875 1558265 Inpp5k inositol polyphosphate 5-phosphatase K gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558265 Inpp5k inositol polyphosphate 5-phosphatase K gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:18573875 1558266 Sec1 secretory blood group 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1558266 Sec1 secretory blood group 1 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20220804 MGI PMID:35696408 1558269 Wnt16 wingless-type MMTV integration site family, member 16 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:22792071 1558269 Wnt16 wingless-type MMTV integration site family, member 16 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:22792071 1558269 Wnt16 wingless-type MMTV integration site family, member 16 gene MP:0021182 decreased femoral compact bone area IAGP N RGD:5509061 20220922 MGI PMID:22792071 1558270 Aff2 AF4/FMR2 family, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11923441 1558270 Aff2 AF4/FMR2 family, member 2 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11923441 1558270 Aff2 AF4/FMR2 family, member 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11923441 1558270 Aff2 AF4/FMR2 family, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11923441 1558270 Aff2 AF4/FMR2 family, member 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11923441 1558270 Aff2 AF4/FMR2 family, member 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:11923441 1558270 Aff2 AF4/FMR2 family, member 2 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11923441 1558270 Aff2 AF4/FMR2 family, member 2 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11923441 1558270 Aff2 AF4/FMR2 family, member 2 gene MP:0004156 abnormal QT variability IEA N RGD:5509061 20230601 MGI 1558270 Aff2 AF4/FMR2 family, member 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1558271 Zcchc2 zinc finger, CCHC domain containing 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1558271 Zcchc2 zinc finger, CCHC domain containing 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1558271 Zcchc2 zinc finger, CCHC domain containing 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 1558271 Zcchc2 zinc finger, CCHC domain containing 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1558272 Ssh2 slingshot protein phosphatase 2 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20221215 MGI 1558272 Ssh2 slingshot protein phosphatase 2 gene MP:0001925 male infertility IEA N RGD:5509061 20220811 MGI 1558272 Ssh2 slingshot protein phosphatase 2 gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20220811 MGI 1558272 Ssh2 slingshot protein phosphatase 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220519 MGI 1558272 Ssh2 slingshot protein phosphatase 2 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1558272 Ssh2 slingshot protein phosphatase 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220519 MGI 1558272 Ssh2 slingshot protein phosphatase 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220519 MGI 1558274 2610028H24Rik RIKEN cDNA 2610028H24 gene gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1558274 2610028H24Rik RIKEN cDNA 2610028H24 gene gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1558275 Ppp1r3a protein phosphatase 1, regulatory subunit 3A gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:12606498 1558275 Ppp1r3a protein phosphatase 1, regulatory subunit 3A gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12606498 1558275 Ppp1r3a protein phosphatase 1, regulatory subunit 3A gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12606498 1558275 Ppp1r3a protein phosphatase 1, regulatory subunit 3A gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12606498 1558275 Ppp1r3a protein phosphatase 1, regulatory subunit 3A gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12606498 1558275 Ppp1r3a protein phosphatase 1, regulatory subunit 3A gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18232732 1558275 Ppp1r3a protein phosphatase 1, regulatory subunit 3A gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:12606498 1558275 Ppp1r3a protein phosphatase 1, regulatory subunit 3A gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11283248 1558275 Ppp1r3a protein phosphatase 1, regulatory subunit 3A gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:12606498 1558275 Ppp1r3a protein phosphatase 1, regulatory subunit 3A gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12606498 1558275 Ppp1r3a protein phosphatase 1, regulatory subunit 3A gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20191226 MGI PMID:11283248 1558275 Ppp1r3a protein phosphatase 1, regulatory subunit 3A gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20191226 MGI PMID:12606498 1558275 Ppp1r3a protein phosphatase 1, regulatory subunit 3A gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20191226 MGI PMID:18232732 1558275 Ppp1r3a protein phosphatase 1, regulatory subunit 3A gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20170803 MGI PMID:12606498 1558275 Ppp1r3a protein phosphatase 1, regulatory subunit 3A gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:12606498 1558276 Acad8 acyl-Coenzyme A dehydrogenase family, member 8 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20151112 MGI PMID:21659959 1558276 Acad8 acyl-Coenzyme A dehydrogenase family, member 8 gene MP:0003978 decreased circulating carnitine level IAGP N RGD:5509061 20151112 MGI PMID:21659959 1558276 Acad8 acyl-Coenzyme A dehydrogenase family, member 8 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20151112 MGI PMID:21659959 1558276 Acad8 acyl-Coenzyme A dehydrogenase family, member 8 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20151112 MGI PMID:21659959 1558276 Acad8 acyl-Coenzyme A dehydrogenase family, member 8 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20151112 MGI PMID:21659959 1558276 Acad8 acyl-Coenzyme A dehydrogenase family, member 8 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20151112 MGI PMID:21659959 1558276 Acad8 acyl-Coenzyme A dehydrogenase family, member 8 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20151112 MGI PMID:21659959 1558276 Acad8 acyl-Coenzyme A dehydrogenase family, member 8 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20151112 MGI PMID:21659959 1558276 Acad8 acyl-Coenzyme A dehydrogenase family, member 8 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20151112 MGI PMID:21659959 1558276 Acad8 acyl-Coenzyme A dehydrogenase family, member 8 gene MP:0011637 abnormal mitochondrial matrix morphology IAGP N RGD:5509061 20151112 MGI PMID:21659959 1558276 Acad8 acyl-Coenzyme A dehydrogenase family, member 8 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:21659959 1558276 Acad8 acyl-Coenzyme A dehydrogenase family, member 8 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21659959 1558276 Acad8 acyl-Coenzyme A dehydrogenase family, member 8 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21659959 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20161201 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20201022 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230119 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0001406 abnormal gait IEA N RGD:5509061 20161201 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0002626 increased heart rate IEA N RGD:5509061 20240523 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20230119 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0002834 decreased heart weight IEA N RGD:5509061 20161201 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20240523 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20230119 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230119 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0005387 immune system phenotype IEA N RGD:5509061 20230119 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20240523 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230119 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20161201 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20230119 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20230119 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0011971 increased circulating lactate dehydrogenase level IEA N RGD:5509061 20211021 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0013510 decreased CD4-negative NK T cell number IEA N RGD:5509061 20230119 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0013669 decreased Ly6C-positive immature NK cell number IEA N RGD:5509061 20230119 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0013678 decreased Ly6C-positive NK T cell number IEA N RGD:5509061 20230119 MGI 1558277 Ube3c ubiquitin protein ligase E3C gene MP:0013691 decreased CD5-positive Ly6C-positive T cell number IEA N RGD:5509061 20230119 MGI 1558278 Rnase12 ribonuclease, RNase A family, 12 (non-active) gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1558278 Rnase12 ribonuclease, RNase A family, 12 (non-active) gene MP:0000274 enlarged heart IEA N RGD:5509061 20201022 MGI 1558278 Rnase12 ribonuclease, RNase A family, 12 (non-active) gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1558278 Rnase12 ribonuclease, RNase A family, 12 (non-active) gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1558278 Rnase12 ribonuclease, RNase A family, 12 (non-active) gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20201022 MGI 1558278 Rnase12 ribonuclease, RNase A family, 12 (non-active) gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20201022 MGI 1558279 Hoxc4 homeobox C4 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:8626021 1558279 Hoxc4 homeobox C4 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:19363484 1558279 Hoxc4 homeobox C4 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:19363484 1558279 Hoxc4 homeobox C4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8660891 1558279 Hoxc4 homeobox C4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:19363484 1558279 Hoxc4 homeobox C4 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:8626021 1558279 Hoxc4 homeobox C4 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:8626021 1558279 Hoxc4 homeobox C4 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:8660891 1558279 Hoxc4 homeobox C4 gene MP:0003159 abnormal esophageal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8660891 1558279 Hoxc4 homeobox C4 gene MP:0004323 sternum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8660891 1558279 Hoxc4 homeobox C4 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:8660891 1558279 Hoxc4 homeobox C4 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:8660891 1558279 Hoxc4 homeobox C4 gene MP:0004679 xiphoid process foramen IAGP N RGD:5509061 20141003 MGI PMID:8626021 1558279 Hoxc4 homeobox C4 gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:19363484 1558279 Hoxc4 homeobox C4 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:19363484 1558279 Hoxc4 homeobox C4 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:8626021 1558279 Hoxc4 homeobox C4 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:8660891 1558279 Hoxc4 homeobox C4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19363484 1558279 Hoxc4 homeobox C4 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:19363484 1558279 Hoxc4 homeobox C4 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:19363484 1558279 Hoxc4 homeobox C4 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:19363484 1558279 Hoxc4 homeobox C4 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:8660891 1558279 Hoxc4 homeobox C4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8660891 1558279 Hoxc4 homeobox C4 gene MP:0012284 increased sternebra number IAGP N RGD:5509061 20141003 MGI PMID:8626021 1558280 Vwa2 von Willebrand factor A domain containing 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1558280 Vwa2 von Willebrand factor A domain containing 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1558280 Vwa2 von Willebrand factor A domain containing 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1558281 Gimap7 GTPase, IMAP family member 7 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 1558281 Gimap7 GTPase, IMAP family member 7 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20240523 MGI 1558281 Gimap7 GTPase, IMAP family member 7 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20240523 MGI 1558281 Gimap7 GTPase, IMAP family member 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 1558283 Lyg1 lysozyme G-like 1 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20190912 MGI PMID:28507796 1558283 Lyg1 lysozyme G-like 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190912 MGI PMID:28507796 1558283 Lyg1 lysozyme G-like 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20190912 MGI PMID:28507796 1558283 Lyg1 lysozyme G-like 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20190912 MGI PMID:28507796 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22898778 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:22898778 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:22898778 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:22898778 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:22898778 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0003542 abnormal vascular endothelial cell development IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0004038 lymphangiectasis IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0010195 abnormal lymphatic vessel endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22898778 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22898778 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22898778 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0012080 chylous ascites IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0012511 dilated aortic sac IAGP N RGD:5509061 20141003 MGI PMID:19151727 1558285 Heg1 heart development protein with EGF-like domains 1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:22898778 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20160804 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20210520 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20160804 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20190808 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20160811 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:23870131 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200514 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0001147 small testis IEA N RGD:5509061 20200514 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20160421 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20190502 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20160421 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20230601 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23870131 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20190808 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0002311 abnormal inspiratory capacity IEA N RGD:5509061 20200514 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20200514 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20230601 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20230601 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:23870131 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20240523 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20160804 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0003393 decreased cardiac output IEA N RGD:5509061 20190502 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210826 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20160421 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0003929 decreased heart rate variability IEA N RGD:5509061 20210826 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160421 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20210826 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20200514 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160421 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20211021 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210128 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20210826 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170105 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20141003 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20170105 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20230601 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:23870131 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20170105 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0009454 impaired contextual conditioning behavior IEA N RGD:5509061 20231207 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160811 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20160421 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20161201 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0010895 increased lung compliance IEA N RGD:5509061 20200514 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20190502 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20160421 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20160421 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20211021 MGI 1558286 Ap4e1 adaptor-related protein complex AP-4, epsilon 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1558287 Adam5 a disintegrin and metallopeptidase domain 5 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1558287 Adam5 a disintegrin and metallopeptidase domain 5 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1558288 Aspn asporin gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1558288 Aspn asporin gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20190502 MGI 1558288 Aspn asporin gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1558288 Aspn asporin gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1558288 Aspn asporin gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20231221 MGI PMID:28859141 1558288 Aspn asporin gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1558288 Aspn asporin gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1558288 Aspn asporin gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1558288 Aspn asporin gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1558288 Aspn asporin gene MP:0005275 abnormal skin tensile strength IAGP N RGD:5509061 20231221 MGI PMID:28859141 1558288 Aspn asporin gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20231221 MGI PMID:28859141 1558288 Aspn asporin gene MP:0011475 abnormal glycosaminoglycan level IAGP N RGD:5509061 20231221 MGI PMID:28859141 1558289 Was Wiskott-Aldrich syndrome gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19805221 1558289 Was Wiskott-Aldrich syndrome gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9697838 1558289 Was Wiskott-Aldrich syndrome gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19805221 1558289 Was Wiskott-Aldrich syndrome gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14645152 1558289 Was Wiskott-Aldrich syndrome gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17878299 1558289 Was Wiskott-Aldrich syndrome gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:9697838 1558289 Was Wiskott-Aldrich syndrome gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20141003 MGI PMID:9697838 1558289 Was Wiskott-Aldrich syndrome gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19805221 1558289 Was Wiskott-Aldrich syndrome gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17878299 1558289 Was Wiskott-Aldrich syndrome gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:14726392 1558289 Was Wiskott-Aldrich syndrome gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10544204 1558289 Was Wiskott-Aldrich syndrome gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:22079330 1558289 Was Wiskott-Aldrich syndrome gene MP:0002223 lymphoid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10544204 1558289 Was Wiskott-Aldrich syndrome gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19805221 1558289 Was Wiskott-Aldrich syndrome gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12730112 1558289 Was Wiskott-Aldrich syndrome gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17878299 1558289 Was Wiskott-Aldrich syndrome gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17878299 1558289 Was Wiskott-Aldrich syndrome gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23305739 1558289 Was Wiskott-Aldrich syndrome gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14645152 1558289 Was Wiskott-Aldrich syndrome gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11070165 1558289 Was Wiskott-Aldrich syndrome gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:12807484 1558289 Was Wiskott-Aldrich syndrome gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11493455 1558289 Was Wiskott-Aldrich syndrome gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22079330 1558289 Was Wiskott-Aldrich syndrome gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:22079330 1558289 Was Wiskott-Aldrich syndrome gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19805221 1558289 Was Wiskott-Aldrich syndrome gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:22079330 1558289 Was Wiskott-Aldrich syndrome gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:17878299 1558289 Was Wiskott-Aldrich syndrome gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:9697838 1558289 Was Wiskott-Aldrich syndrome gene MP:0002827 abnormal renal corpuscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:22079330 1558289 Was Wiskott-Aldrich syndrome gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:14645152 1558289 Was Wiskott-Aldrich syndrome gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:12730112 1558289 Was Wiskott-Aldrich syndrome gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:10544204 1558289 Was Wiskott-Aldrich syndrome gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19805221 1558289 Was Wiskott-Aldrich syndrome gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:9697838 1558289 Was Wiskott-Aldrich syndrome gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:17878299 1558289 Was Wiskott-Aldrich syndrome gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:19805221 1558289 Was Wiskott-Aldrich syndrome gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:17878299 1558289 Was Wiskott-Aldrich syndrome gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19805221 1558289 Was Wiskott-Aldrich syndrome gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10544204 1558289 Was Wiskott-Aldrich syndrome gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9697838 1558289 Was Wiskott-Aldrich syndrome gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10544204 1558289 Was Wiskott-Aldrich syndrome gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9697838 1558289 Was Wiskott-Aldrich syndrome gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10544204 1558289 Was Wiskott-Aldrich syndrome gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17878299 1558289 Was Wiskott-Aldrich syndrome gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19805221 1558289 Was Wiskott-Aldrich syndrome gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9697838 1558289 Was Wiskott-Aldrich syndrome gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10544204 1558289 Was Wiskott-Aldrich syndrome gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12807484 1558289 Was Wiskott-Aldrich syndrome gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19805221 1558289 Was Wiskott-Aldrich syndrome gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9697838 1558289 Was Wiskott-Aldrich syndrome gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0005461 abnormal dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19805221 1558289 Was Wiskott-Aldrich syndrome gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19805221 1558289 Was Wiskott-Aldrich syndrome gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17878299 1558289 Was Wiskott-Aldrich syndrome gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17878299 1558289 Was Wiskott-Aldrich syndrome gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:19805221 1558289 Was Wiskott-Aldrich syndrome gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22302739 1558289 Was Wiskott-Aldrich syndrome gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:14726392 1558289 Was Wiskott-Aldrich syndrome gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:19805221 1558289 Was Wiskott-Aldrich syndrome gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:22079330 1558289 Was Wiskott-Aldrich syndrome gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:22079330 1558289 Was Wiskott-Aldrich syndrome gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:22079330 1558289 Was Wiskott-Aldrich syndrome gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:22079330 1558290 Hars2 histidyl-tRNA synthetase 2 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20240919 MGI 1558290 Hars2 histidyl-tRNA synthetase 2 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20240919 MGI 1558290 Hars2 histidyl-tRNA synthetase 2 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20240919 MGI 1558290 Hars2 histidyl-tRNA synthetase 2 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20240919 MGI 1558290 Hars2 histidyl-tRNA synthetase 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1558290 Hars2 histidyl-tRNA synthetase 2 gene MP:0009331 absent primitive node IEA N RGD:5509061 20240919 MGI 1558290 Hars2 histidyl-tRNA synthetase 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1558290 Hars2 histidyl-tRNA synthetase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558290 Hars2 histidyl-tRNA synthetase 2 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IEA N RGD:5509061 20241017 MGI 1558290 Hars2 histidyl-tRNA synthetase 2 gene MP:0012724 absent head fold IEA N RGD:5509061 20240919 MGI 1558290 Hars2 histidyl-tRNA synthetase 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1558291 Snx27 sorting nexin family member 27 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20221215 MGI 1558291 Snx27 sorting nexin family member 27 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20190808 MGI 1558291 Snx27 sorting nexin family member 27 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21300787 1558291 Snx27 sorting nexin family member 27 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:21300787 1558291 Snx27 sorting nexin family member 27 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:21300787 1558291 Snx27 sorting nexin family member 27 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21300787 1558291 Snx27 sorting nexin family member 27 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1558291 Snx27 sorting nexin family member 27 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:21300787 1558291 Snx27 sorting nexin family member 27 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1558291 Snx27 sorting nexin family member 27 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1558291 Snx27 sorting nexin family member 27 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21300787 1558291 Snx27 sorting nexin family member 27 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21300787 1558291 Snx27 sorting nexin family member 27 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21300787 1558291 Snx27 sorting nexin family member 27 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21300787 1558291 Snx27 sorting nexin family member 27 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558293 Zc3h7a zinc finger CCCH type containing 7 A gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1558293 Zc3h7a zinc finger CCCH type containing 7 A gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1558293 Zc3h7a zinc finger CCCH type containing 7 A gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1558293 Zc3h7a zinc finger CCCH type containing 7 A gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 1558293 Zc3h7a zinc finger CCCH type containing 7 A gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1558293 Zc3h7a zinc finger CCCH type containing 7 A gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1558293 Zc3h7a zinc finger CCCH type containing 7 A gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220519 MGI 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20220811 MGI 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20240523 MGI 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0000745 tremors IAGP N RGD:5509061 20241017 MGI PMID:35760530 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220811 MGI 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0002626 increased heart rate IEA N RGD:5509061 20211021 MGI 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210826 MGI 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20241017 MGI PMID:35760530 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0005473 decreased triiodothyronine level IAGP N RGD:5509061 20241017 MGI PMID:35760530 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20210826 MGI 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0005655 increased aggression IEA N RGD:5509061 20220811 MGI 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20241017 MGI PMID:35760530 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210826 MGI 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210826 MGI 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20241017 MGI PMID:35760530 1558294 Secisbp2l SECIS binding protein 2-like gene MP:0014318 abnormal oligodendrocyte differentiation IAGP N RGD:5509061 20241017 MGI PMID:35760530 1558295 Amot angiomotin gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17699752 1558295 Amot angiomotin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17699752 1558295 Amot angiomotin gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12676095 1558295 Amot angiomotin gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12676095 1558295 Amot angiomotin gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17699752 1558295 Amot angiomotin gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:17699752 1558295 Amot angiomotin gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12676095 1558295 Amot angiomotin gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:17699752 1558295 Amot angiomotin gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:17699752 1558295 Amot angiomotin gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17699752 1558295 Amot angiomotin gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12676095 1558295 Amot angiomotin gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17699752 1558295 Amot angiomotin gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12676095 1558295 Amot angiomotin gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20141003 MGI PMID:12676095 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210520 MGI 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0000649 sebaceous gland atrophy IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0001192 scaly skin IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0001212 skin lesions IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0001310 abnormal conjunctiva morphology IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20221117 MGI PMID:34113821 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0001337 dry eyes IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0001337 dry eyes IAGP N RGD:5509061 20221117 MGI PMID:34113821 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0001349 excessive tearing IAGP N RGD:5509061 20221117 MGI PMID:34113821 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0001851 eye inflammation IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210520 MGI 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0001994 increased blinking frequency IAGP N RGD:5509061 20221117 MGI PMID:34113821 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0003853 dry skin IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0004222 iris synechia IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0005251 blepharitis IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0005252 abnormal Meibomian gland morphology IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0005252 abnormal Meibomian gland morphology IAGP N RGD:5509061 20221117 MGI PMID:34113821 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20221215 MGI 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0006193 conjunctival telangiectasia IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0009935 abnormal Meibomian gland acinus morphology IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0010202 focal dorsal hair loss IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0010699 dilated hair follicle IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0013145 eye discharge IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0013192 decreased sebaceous gland number IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0013375 abnormal sebocyte morphology IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0013386 enlarged Meibomian gland IAGP N RGD:5509061 20221117 MGI PMID:34113821 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0013391 abnormal Meibomian gland physiology IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0013391 abnormal Meibomian gland physiology IAGP N RGD:5509061 20221117 MGI PMID:34113821 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0014131 abnormal tear film morphology IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0014131 abnormal tear film morphology IAGP N RGD:5509061 20221117 MGI PMID:34113821 1558296 Awat2 acyl-CoA wax alcohol acyltransferase 2 gene MP:0014154 Meibomian gland degeneration IAGP N RGD:5509061 20210819 MGI PMID:32851726 1558297 Prss50 serine protease 50 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20141003 MGI 1558297 Prss50 serine protease 50 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210603 MGI PMID:33913480 1558297 Prss50 serine protease 50 gene MP:0001925 male infertility IAGP N RGD:5509061 20210603 MGI PMID:33913480 1558297 Prss50 serine protease 50 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20210603 MGI PMID:33913480 1558297 Prss50 serine protease 50 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20210603 MGI PMID:33913480 1558297 Prss50 serine protease 50 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220714 MGI PMID:33913480 1558297 Prss50 serine protease 50 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1558297 Prss50 serine protease 50 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20160804 MGI 1558297 Prss50 serine protease 50 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210603 MGI PMID:33913480 1558297 Prss50 serine protease 50 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210603 MGI PMID:33913480 1558297 Prss50 serine protease 50 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20141003 MGI 1558297 Prss50 serine protease 50 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20210603 MGI PMID:33913480 1558297 Prss50 serine protease 50 gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20220714 MGI PMID:33913480 1558297 Prss50 serine protease 50 gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20210603 MGI PMID:33913480 1558297 Prss50 serine protease 50 gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20210603 MGI PMID:33913480 1558297 Prss50 serine protease 50 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20210603 MGI PMID:33913480 1558297 Prss50 serine protease 50 gene MP:0009839 multiflagellated sperm IAGP N RGD:5509061 20220630 MGI PMID:33913480 1558297 Prss50 serine protease 50 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220714 MGI PMID:33913480 1558297 Prss50 serine protease 50 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220714 MGI PMID:33913480 1558297 Prss50 serine protease 50 gene MP:0031408 multi-headed sperm IAGP N RGD:5509061 20220630 MGI PMID:33913480 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:19837033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:8789439 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:8789439 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:12040033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:8789439 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12040033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19837032 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19837033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12040033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:12040033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:19837033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8789439 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8789439 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8789439 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8789439 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20141003 MGI PMID:12040033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0004367 abnormal strial intermediate cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12040033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0004368 abnormal stria vascularis vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12040033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12040033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12040033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0004487 type I spiral ligament fibrocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:12040033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12040033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12040033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0004758 absent strial marginal cells IAGP N RGD:5509061 20141003 MGI PMID:12040033 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19837032 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8789439 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0006200 vitreous body deposition IAGP N RGD:5509061 20141003 MGI PMID:8789439 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0008509 disorganized retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:8789439 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:8789439 1558298 Ndp Norrie disease (pseudoglioma) (human) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12040033 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17124501 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0000861 disorganized barrel cortex IAGP N RGD:5509061 20141003 MGI PMID:16525048 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17124501 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:17124501 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:11797009 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11797010 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:11797010 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:16525048 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:19074017 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19074017 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21241895 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11797009 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16525048 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:11797009 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20141003 MGI PMID:17124501 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0002918 abnormal paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:11797009 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:11797009 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:19074017 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:11797009 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0002921 abnormal post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:11797009 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19074017 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:21241895 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:19074017 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21241895 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:17124501 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:17124501 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:17124501 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0010104 enlarged thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:17124501 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19074017 1558300 Rims1 regulating synaptic membrane exocytosis 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17124501 1558305 Gmip Gem-interacting protein gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1558307 Cd160 CD160 antigen gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200723 MGI PMID:32231122 1558307 Cd160 CD160 antigen gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20160128 MGI PMID:25711213 1558307 Cd160 CD160 antigen gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20160128 MGI PMID:25711213 1558308 Nhlrc3 NHL repeat containing 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1558308 Nhlrc3 NHL repeat containing 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1558308 Nhlrc3 NHL repeat containing 3 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1558310 C1ql3 C1q-like 3 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1558310 C1ql3 C1q-like 3 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20230601 MGI 1558310 C1ql3 C1q-like 3 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20230601 MGI 1558310 C1ql3 C1q-like 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20161020 MGI PMID:27478018 1558310 C1ql3 C1q-like 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20161020 MGI PMID:27478018 1558310 C1ql3 C1q-like 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20161020 MGI PMID:27478018 1558310 C1ql3 C1q-like 3 gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20161020 MGI PMID:27478018 1558310 C1ql3 C1q-like 3 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20230601 MGI 1558310 C1ql3 C1q-like 3 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20230601 MGI 1558310 C1ql3 C1q-like 3 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20230601 MGI 1558310 C1ql3 C1q-like 3 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20161020 MGI PMID:27478018 1558310 C1ql3 C1q-like 3 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20161020 MGI PMID:27478018 1558310 C1ql3 C1q-like 3 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20161020 MGI PMID:27478018 1558310 C1ql3 C1q-like 3 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20161020 MGI PMID:27478018 1558311 Cyp2b10 cytochrome P450, family 2, subfamily b, polypeptide 10 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20231019 MGI PMID:36224745 1558311 Cyp2b10 cytochrome P450, family 2, subfamily b, polypeptide 10 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20231019 MGI PMID:36224745 1558311 Cyp2b10 cytochrome P450, family 2, subfamily b, polypeptide 10 gene MP:0005443 abnormal ethanol metabolism IAGP N RGD:5509061 20231019 MGI PMID:36224745 1558311 Cyp2b10 cytochrome P450, family 2, subfamily b, polypeptide 10 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20231019 MGI PMID:36224745 1558311 Cyp2b10 cytochrome P450, family 2, subfamily b, polypeptide 10 gene MP:0010951 abnormal lipid oxidation IAGP N RGD:5509061 20231019 MGI PMID:36224745 1558311 Cyp2b10 cytochrome P450, family 2, subfamily b, polypeptide 10 gene MP:0031267 increased susceptibility to alcohol-induced hepatic steatosis IAGP N RGD:5509061 20231019 MGI PMID:36224745 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0001349 excessive tearing IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12815074 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0005034 abnormal anus morphology IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0006167 eyelid edema IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:12815074 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0009859 eye opacity IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11809813 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12815074 1558312 Rad23b RAD23 homolog B, nucleotide excision repair protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12815074 1558313 Ninl ninein-like gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1558313 Ninl ninein-like gene MP:0013415 increased myeloid cell number in bone marrow IAGP N RGD:5509061 20160915 MGI PMID:24652767 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20191205 MGI PMID:31242448 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20191205 MGI PMID:31242448 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20180412 MGI PMID:28145888 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180412 MGI PMID:28145888 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20180412 MGI PMID:28145888 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0001304 cataract IEA N RGD:5509061 20150430 MGI 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0001919 abnormal reproductive system physiology IEA N RGD:5509061 20141003 MGI 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20191205 MGI PMID:31242448 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20231207 MGI 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20191205 MGI PMID:31242448 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0003641 small lung IAGP N RGD:5509061 20191205 MGI PMID:31242448 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20180412 MGI PMID:28145888 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20180412 MGI PMID:28145888 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20231207 MGI 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20180412 MGI PMID:28145888 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180412 MGI PMID:28145888 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0009571 abnormal right lung accessory lobe morphology IAGP N RGD:5509061 20191205 MGI PMID:31242448 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20191205 MGI PMID:31242448 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20191205 MGI PMID:31242448 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0011289 abnormal nephron number IAGP N RGD:5509061 20191205 MGI PMID:31242448 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0011493 double ureter IAGP N RGD:5509061 20191205 MGI PMID:31242448 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20180412 MGI PMID:28145888 1558314 Adamts18 ADAM metallopeptidase with thrombospondin type 1 motif 18 gene MP:0014222 decreased colon goblet cell number IAGP N RGD:5509061 20180412 MGI PMID:28145888 1558319 Zfp786 zinc finger protein 786 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1558320 Cldn2 claudin 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:20385797 1558320 Cldn2 claudin 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:20385797 1558320 Cldn2 claudin 2 gene MP:0004041 increased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20170713 MGI PMID:27214555 1558320 Cldn2 claudin 2 gene MP:0005039 hypoxia IAGP N RGD:5509061 20170713 MGI PMID:27214555 1558320 Cldn2 claudin 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20170713 MGI PMID:27214555 1558320 Cldn2 claudin 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20170713 MGI PMID:27214555 1558320 Cldn2 claudin 2 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:20385797 1558320 Cldn2 claudin 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20170713 MGI PMID:27214555 1558320 Cldn2 claudin 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20170713 MGI PMID:27214555 1558320 Cldn2 claudin 2 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:20385797 1558320 Cldn2 claudin 2 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20170713 MGI PMID:27214555 1558320 Cldn2 claudin 2 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:20385797 1558320 Cldn2 claudin 2 gene MP:0010108 abnormal renal water reabsorption IAGP N RGD:5509061 20141003 MGI PMID:20385797 1558320 Cldn2 claudin 2 gene MP:0010109 abnormal renal sodium reabsorption IAGP N RGD:5509061 20141003 MGI PMID:20385797 1558320 Cldn2 claudin 2 gene MP:0010109 abnormal renal sodium reabsorption IAGP N RGD:5509061 20170713 MGI PMID:27214555 1558320 Cldn2 claudin 2 gene MP:0011442 abnormal renal sodium ion transport IAGP N RGD:5509061 20170713 MGI PMID:27214555 1558321 Lrrc25 leucine rich repeat containing 25 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20210415 MGI PMID:30340835 1558321 Lrrc25 leucine rich repeat containing 25 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20210415 MGI PMID:30340835 1558321 Lrrc25 leucine rich repeat containing 25 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20210415 MGI PMID:30340835 1558321 Lrrc25 leucine rich repeat containing 25 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20210415 MGI PMID:30340835 1558321 Lrrc25 leucine rich repeat containing 25 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20210415 MGI PMID:30340835 1558321 Lrrc25 leucine rich repeat containing 25 gene MP:0008837 increased transforming growth factor beta level IAGP N RGD:5509061 20210415 MGI PMID:30340835 1558321 Lrrc25 leucine rich repeat containing 25 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:30340835 1558322 Sp9 trans-acting transcription factor 9 gene MP:0000746 weakness IAGP N RGD:5509061 20180705 MGI PMID:27452460 1558322 Sp9 trans-acting transcription factor 9 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20180705 MGI PMID:27452460 1558322 Sp9 trans-acting transcription factor 9 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20180705 MGI PMID:27452460 1558322 Sp9 trans-acting transcription factor 9 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20180705 MGI PMID:27452460 1558322 Sp9 trans-acting transcription factor 9 gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20180705 MGI PMID:27452460 1558322 Sp9 trans-acting transcription factor 9 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180705 MGI PMID:27452460 1558322 Sp9 trans-acting transcription factor 9 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20180705 MGI PMID:27452460 1558322 Sp9 trans-acting transcription factor 9 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20180705 MGI PMID:27452460 1558322 Sp9 trans-acting transcription factor 9 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:27452460 1558325 Serp2 stress-associated endoplasmic reticulum protein family member 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 1558327 Cnih4 cornichon family AMPA receptor auxiliary protein 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230309 MGI PMID:36657507 1558327 Cnih4 cornichon family AMPA receptor auxiliary protein 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230309 MGI PMID:36657507 1558327 Cnih4 cornichon family AMPA receptor auxiliary protein 4 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230309 MGI PMID:36657507 1558328 Dnaaf9 dynein axonemal assembly factor 9 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 1558328 Dnaaf9 dynein axonemal assembly factor 9 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210826 MGI 1558331 Serpina6 serine (or cysteine) peptidase inhibitor, clade A, member 6 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16980625 1558331 Serpina6 serine (or cysteine) peptidase inhibitor, clade A, member 6 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:20022933 1558331 Serpina6 serine (or cysteine) peptidase inhibitor, clade A, member 6 gene MP:0005129 increased adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:16980625 1558331 Serpina6 serine (or cysteine) peptidase inhibitor, clade A, member 6 gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:16980625 1558331 Serpina6 serine (or cysteine) peptidase inhibitor, clade A, member 6 gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:20022933 1558331 Serpina6 serine (or cysteine) peptidase inhibitor, clade A, member 6 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:16980625 1558331 Serpina6 serine (or cysteine) peptidase inhibitor, clade A, member 6 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16980625 1558331 Serpina6 serine (or cysteine) peptidase inhibitor, clade A, member 6 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:20022933 1558331 Serpina6 serine (or cysteine) peptidase inhibitor, clade A, member 6 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:16980625 1558332 H2-T23 histocompatibility 2, T region locus 23 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180719 MGI PMID:15098030 1558332 H2-T23 histocompatibility 2, T region locus 23 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20180719 MGI PMID:15098030 1558332 H2-T23 histocompatibility 2, T region locus 23 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180719 MGI PMID:15098030 1558332 H2-T23 histocompatibility 2, T region locus 23 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180719 MGI PMID:19047627 1558332 H2-T23 histocompatibility 2, T region locus 23 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180719 MGI PMID:19047627 1558332 H2-T23 histocompatibility 2, T region locus 23 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20180719 MGI PMID:17509909 1558332 H2-T23 histocompatibility 2, T region locus 23 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20180719 MGI PMID:19047627 1558332 H2-T23 histocompatibility 2, T region locus 23 gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20180719 MGI PMID:17509909 1558332 H2-T23 histocompatibility 2, T region locus 23 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:15098030 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:20566848 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20566848 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:20566848 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20566848 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20566848 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:20566848 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0001889 delayed brain development IAGP N RGD:5509061 20141003 MGI PMID:20566848 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:20566848 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:20566848 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:20566848 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20210128 MGI 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20566848 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0009782 abnormal basicranium angle IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0010208 prognathia IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20566848 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:20566848 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:23277562 1558333 Smg1 SMG1 nonsense mediated mRNA decay associated PI3K related kinase gene MP:0030241 absent optic pit IAGP N RGD:5509061 20171109 MGI PMID:20566848 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:17609388 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:17609388 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17609388 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:17609388 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:17609388 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20181227 MGI 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:15386003 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:22976293 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17609388 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:15386003 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22976293 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15386003 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18188447 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20855869 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:15386003 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:15386003 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15386003 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17609388 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17609388 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15386003 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:22976293 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:17609388 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20855869 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:17609388 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20855869 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:23372168 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22976293 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17609388 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:20855869 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20855869 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:20855869 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17609388 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:15386003 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:22976293 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0009548 abnormal platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:23372168 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15386003 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22976293 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17609388 1558334 Pip5k1c phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558335 Derl3 Der1-like domain family, member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11422294 1558336 Ngdn neuroguidin, EIF4E binding protein gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1558336 Ngdn neuroguidin, EIF4E binding protein gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20220811 MGI 1558336 Ngdn neuroguidin, EIF4E binding protein gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1558336 Ngdn neuroguidin, EIF4E binding protein gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1558336 Ngdn neuroguidin, EIF4E binding protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12387738 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16530702 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12387738 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0002220 large lymphoid organs IAGP N RGD:5509061 20141003 MGI PMID:12387738 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0002418 increased susceptibility to viral infection IAGP N RGD:5509061 20221222 MGI PMID:35266071 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20221222 MGI PMID:35266071 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12387738 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:12387738 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16530702 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:16530702 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12387738 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:12387738 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:12387738 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12387738 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12387738 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:12387738 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:12387738 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20221229 MGI PMID:35266071 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20221222 MGI PMID:35266071 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20221222 MGI PMID:35266071 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20221222 MGI PMID:35266071 1558337 Elf4 E74 like ETS transcription factor 4 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12387738 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:10615132 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:9568711 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:19235720 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:21307093 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18782757 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:20093497 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:19235720 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:20862291 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:21307093 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0000650 mesocardia IAGP N RGD:5509061 20141003 MGI PMID:19235720 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0001270 distended abdomen IEA N RGD:5509061 20151112 MGI 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:21307093 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18782757 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19235720 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20862291 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21307093 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10615132 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20862291 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20862291 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10615132 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002083 premature death IAGP N RGD:5509061 20151203 MGI PMID:25574838 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002083 premature death IAGP N RGD:5509061 20181129 MGI PMID:28244683 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002083 premature death IAGP N RGD:5509061 20190725 MGI PMID:28205547 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20181129 MGI PMID:28244683 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20862291 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21307093 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:10615132 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18235088 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18782757 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:19235720 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:20862291 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002767 situs ambiguus IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20093497 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:20093497 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20181129 MGI PMID:28244683 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20190725 MGI PMID:28205547 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:19235720 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:20862291 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20141003 MGI PMID:18782757 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20141003 MGI PMID:20093497 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20141003 MGI PMID:9568711 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:10615132 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:12140187 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:18782757 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:20093497 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:9568711 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003327 liver cyst IAGP N RGD:5509061 20181129 MGI PMID:28244683 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20093497 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:10615132 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:18782757 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:20862291 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20181129 MGI PMID:28244683 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:10615132 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003606 kidney failure IAGP N RGD:5509061 20181129 MGI PMID:28244683 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:10615132 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:12140187 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18235088 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18782757 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:20181743 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:20862291 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:21685914 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:9568711 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003675 kidney cyst IAGP N RGD:5509061 20181129 MGI PMID:28244683 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003675 kidney cyst IAGP N RGD:5509061 20190725 MGI PMID:28205547 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003675 kidney cyst IAGP N RGD:5509061 20210603 MGI PMID:28750036 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:20093497 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:21685914 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20151203 MGI PMID:25574838 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0004020 polyhydramnios IAGP N RGD:5509061 20141003 MGI PMID:16301212 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0004020 polyhydramnios IAGP N RGD:5509061 20141003 MGI PMID:20862291 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:12859898 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:23357539 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:21307093 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:19959710 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:10615132 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20181129 MGI PMID:28244683 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20190725 MGI PMID:28205547 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20190725 MGI PMID:28205547 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:10615132 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:21685914 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20151203 MGI PMID:25574838 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20181129 MGI PMID:28244683 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20190725 MGI PMID:28205547 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:10615132 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:20093497 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:9568711 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20151203 MGI PMID:25574838 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20190725 MGI PMID:28205547 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16301212 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:18782757 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:18782757 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:19959710 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:10615132 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:10615132 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:10615132 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0010439 abnormal hepatic vein morphology IAGP N RGD:5509061 20141003 MGI PMID:18782757 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0010807 abnormal stomach position or orientation IAGP N RGD:5509061 20141003 MGI PMID:19235720 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:21307093 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20862291 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20862291 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12062060 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10615132 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20181743 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20862291 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21307093 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23357539 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20862291 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23357539 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20141003 MGI PMID:9568711 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011331 abnormal papillary duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18782757 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20093497 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20093497 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20181129 MGI PMID:28244683 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20190725 MGI PMID:28205547 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20190725 MGI PMID:28205547 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:18782757 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0012172 abnormal amniotic fluid composition IAGP N RGD:5509061 20141003 MGI PMID:16301212 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0012236 abnormal cholangiocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20093497 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0012237 increased cholangiocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20093497 1558338 Pkd2 polycystin 2, transient receptor potential cation channel gene MP:0012238 abnormal cholangiocyte primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:20093497 1558339 Erbin Erbb2 interacting protein gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:19458253 1558339 Erbin Erbb2 interacting protein gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:19458253 1558339 Erbin Erbb2 interacting protein gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19458253 1558339 Erbin Erbb2 interacting protein gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:19458253 1558339 Erbin Erbb2 interacting protein gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:19458253 1558341 Gata5 GATA binding protein 5 gene MP:0000231 hypertension IAGP N RGD:5509061 20160225 MGI PMID:26617239 1558341 Gata5 GATA binding protein 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20240118 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10866681 1558341 Gata5 GATA binding protein 5 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0001139 abnormal vagina morphology IAGP N RGD:5509061 20141003 MGI PMID:10866681 1558341 Gata5 GATA binding protein 5 gene MP:0001140 abnormal vagina epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10866681 1558341 Gata5 GATA binding protein 5 gene MP:0001142 abnormal vagina orifice morphology IAGP N RGD:5509061 20141003 MGI PMID:10866681 1558341 Gata5 GATA binding protein 5 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20160225 MGI PMID:26617239 1558341 Gata5 GATA binding protein 5 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20160225 MGI PMID:26617239 1558341 Gata5 GATA binding protein 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10866681 1558341 Gata5 GATA binding protein 5 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20160225 MGI PMID:26617239 1558341 Gata5 GATA binding protein 5 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20160225 MGI PMID:26617239 1558341 Gata5 GATA binding protein 5 gene MP:0003315 abnormal perineum morphology IAGP N RGD:5509061 20141003 MGI PMID:10866681 1558341 Gata5 GATA binding protein 5 gene MP:0003316 perineal fistula IAGP N RGD:5509061 20141003 MGI PMID:10866681 1558341 Gata5 GATA binding protein 5 gene MP:0003529 enlarged clitoris IAGP N RGD:5509061 20141003 MGI PMID:10866681 1558341 Gata5 GATA binding protein 5 gene MP:0003541 vaginal inflammation IAGP N RGD:5509061 20141003 MGI PMID:10866681 1558341 Gata5 GATA binding protein 5 gene MP:0003550 short perineum IAGP N RGD:5509061 20141003 MGI PMID:10866681 1558341 Gata5 GATA binding protein 5 gene MP:0003550 short perineum IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20160225 MGI PMID:26617239 1558341 Gata5 GATA binding protein 5 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20160225 MGI PMID:26617239 1558341 Gata5 GATA binding protein 5 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20160225 MGI PMID:26617239 1558341 Gata5 GATA binding protein 5 gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20160225 MGI PMID:26617239 1558341 Gata5 GATA binding protein 5 gene MP:0005583 decreased renin activity IAGP N RGD:5509061 20160225 MGI PMID:26617239 1558341 Gata5 GATA binding protein 5 gene MP:0005600 increased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20160225 MGI PMID:26617239 1558341 Gata5 GATA binding protein 5 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20160225 MGI PMID:26617239 1558341 Gata5 GATA binding protein 5 gene MP:0008727 increased heart right atrium size IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0010408 sinus venosus atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0010419 inlet ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0010428 abnormal heart right ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0010429 abnormal heart left ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0010463 aorta stenosis IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0010587 conotruncal ridge hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0010595 abnormal aortic valve cusp morphology IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0010640 ventricular myocardium compact layer hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20240118 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0011485 abnormal urethra urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10866681 1558341 Gata5 GATA binding protein 5 gene MP:0011572 abnormal aorta bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:21633169 1558341 Gata5 GATA binding protein 5 gene MP:0011673 unbalanced complete common atrioventricular canal IAGP N RGD:5509061 20210708 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0011749 perivascular fibrosis IAGP N RGD:5509061 20160225 MGI PMID:26617239 1558341 Gata5 GATA binding protein 5 gene MP:0011763 urethritis IAGP N RGD:5509061 20141003 MGI PMID:10866681 1558341 Gata5 GATA binding protein 5 gene MP:0011780 abnormal female urethra morphology IAGP N RGD:5509061 20141003 MGI PMID:10866681 1558341 Gata5 GATA binding protein 5 gene MP:0011850 absent clitoral bone IAGP N RGD:5509061 20141003 MGI PMID:10866681 1558341 Gata5 GATA binding protein 5 gene MP:0013313 female preputial gland hypoplasia IAGP N RGD:5509061 20141204 MGI PMID:10866681 1558341 Gata5 GATA binding protein 5 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20191128 MGI PMID:19889636 1558341 Gata5 GATA binding protein 5 gene MP:0031611 decreased fetal cardiomyocyte number IAGP N RGD:5509061 20240321 MGI PMID:21633169 1558342 Sfpq splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated) gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201231 MGI 1558342 Sfpq splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated) gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20191003 MGI PMID:29719248 1558342 Sfpq splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated) gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20191003 MGI PMID:29719248 1558342 Sfpq splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated) gene MP:0001297 microphthalmia IAGP N RGD:5509061 20191003 MGI PMID:29719248 1558342 Sfpq splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated) gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20191003 MGI PMID:29719248 1558342 Sfpq splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated) gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20191003 MGI PMID:29719248 1558342 Sfpq splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated) gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20191003 MGI PMID:29719248 1558342 Sfpq splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated) gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20191003 MGI PMID:29719248 1558342 Sfpq splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated) gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20191003 MGI PMID:29719248 1558342 Sfpq splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated) gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20201022 MGI 1558342 Sfpq splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated) gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22966205 1558342 Sfpq splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated) gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20191003 MGI PMID:29719248 1558342 Sfpq splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated) gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:22966205 1558342 Sfpq splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated) gene MP:0020527 small thalamus IAGP N RGD:5509061 20191003 MGI PMID:29719248 1558343 Snx29 sorting nexin 29 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1558343 Snx29 sorting nexin 29 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1558343 Snx29 sorting nexin 29 gene MP:0011940 decreased food intake IEA N RGD:5509061 20211021 MGI 1558344 Serf1 small EDRK-rich factor 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20141003 MGI 1558344 Serf1 small EDRK-rich factor 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20160804 MGI 1558344 Serf1 small EDRK-rich factor 1 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20160804 MGI 1558344 Serf1 small EDRK-rich factor 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20141003 MGI 1558344 Serf1 small EDRK-rich factor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20160804 MGI 1558346 Setmar SET domain without mariner transposase fusion gene MP:0000745 tremors IEA N RGD:5509061 20141003 MGI 1558346 Setmar SET domain without mariner transposase fusion gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1558346 Setmar SET domain without mariner transposase fusion gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20141003 MGI 1558346 Setmar SET domain without mariner transposase fusion gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20141003 MGI 1558348 Vstm5 V-set and transmembrane domain containing 5 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20240523 MGI 1558348 Vstm5 V-set and transmembrane domain containing 5 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20191107 MGI PMID:30194420 1558349 Lefty1 left right determination factor 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0000542 left-sided isomerism IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20210128 MGI 1558349 Lefty1 left right determination factor 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:12431380 1558349 Lefty1 left right determination factor 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12431380 1558349 Lefty1 left right determination factor 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1558349 Lefty1 left right determination factor 1 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:12431380 1558349 Lefty1 left right determination factor 1 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1558349 Lefty1 left right determination factor 1 gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:12431380 1558349 Lefty1 left right determination factor 1 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1558349 Lefty1 left right determination factor 1 gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1558349 Lefty1 left right determination factor 1 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 1558349 Lefty1 left right determination factor 1 gene MP:0006063 abnormal inferior vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0006123 tricuspid valve atresia IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:12431380 1558349 Lefty1 left right determination factor 1 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1558349 Lefty1 left right determination factor 1 gene MP:0008461 left atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1558349 Lefty1 left right determination factor 1 gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1558349 Lefty1 left right determination factor 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0010425 abnormal heart and great vessel attachment IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0010668 abnormal hepatic portal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558349 Lefty1 left right determination factor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12431380 1558349 Lefty1 left right determination factor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:12431380 1558349 Lefty1 left right determination factor 1 gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20141003 MGI PMID:21364967 1558349 Lefty1 left right determination factor 1 gene MP:0011327 abnormal left renal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0011569 abnormal azygos vein morphology IAGP N RGD:5509061 20141003 MGI PMID:9708731 1558349 Lefty1 left right determination factor 1 gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:12431380 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18285334 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:18285334 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17442931 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18285334 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17442931 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18285334 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17442931 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17442931 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17442931 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17442931 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:18285334 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:17442931 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18285334 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18285334 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18285334 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442931 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:18285334 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442931 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:17442931 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0009341 decreased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17442931 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17442931 1558350 Klf13 Kruppel-like transcription factor 13 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:18285334 1558351 Rnf144a ring finger protein 144A gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20181227 MGI 1558351 Rnf144a ring finger protein 144A gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20240502 MGI PMID:37955227 1558351 Rnf144a ring finger protein 144A gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 1558351 Rnf144a ring finger protein 144A gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20240502 MGI PMID:37955227 1558351 Rnf144a ring finger protein 144A gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20240502 MGI PMID:37955227 1558354 Yipf6 Yip1 domain family, member 6 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20230720 MGI 1558354 Yipf6 Yip1 domain family, member 6 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:22802641 1558354 Yipf6 Yip1 domain family, member 6 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22802641 1558354 Yipf6 Yip1 domain family, member 6 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1558354 Yipf6 Yip1 domain family, member 6 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1558354 Yipf6 Yip1 domain family, member 6 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1558354 Yipf6 Yip1 domain family, member 6 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:22802641 1558354 Yipf6 Yip1 domain family, member 6 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22802641 1558354 Yipf6 Yip1 domain family, member 6 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22802641 1558354 Yipf6 Yip1 domain family, member 6 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:22802641 1558354 Yipf6 Yip1 domain family, member 6 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22802641 1558354 Yipf6 Yip1 domain family, member 6 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22802641 1558354 Yipf6 Yip1 domain family, member 6 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:22802641 1558354 Yipf6 Yip1 domain family, member 6 gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20150611 MGI PMID:22802641 1558355 Scgb3a2 secretoglobin, family 3A, member 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180920 MGI PMID:25242865 1558355 Scgb3a2 secretoglobin, family 3A, member 2 gene MP:0005388 respiratory system phenotype IAGP N RGD:5509061 20210204 MGI PMID:30768367 1558355 Scgb3a2 secretoglobin, family 3A, member 2 gene MP:0011053 decreased respiratory motile cilia number IAGP N RGD:5509061 20210204 MGI PMID:30768367 1558356 Ncapd3 non-SMC condensin II complex, subunit D3 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1558356 Ncapd3 non-SMC condensin II complex, subunit D3 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1558356 Ncapd3 non-SMC condensin II complex, subunit D3 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1558356 Ncapd3 non-SMC condensin II complex, subunit D3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1558356 Ncapd3 non-SMC condensin II complex, subunit D3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1558356 Ncapd3 non-SMC condensin II complex, subunit D3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1558358 Cd300c CD300C molecule gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20181227 MGI 1558358 Cd300c CD300C molecule gene MP:0001258 decreased body length IEA N RGD:5509061 20181227 MGI 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:15860530 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20171012 MGI PMID:25288642 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15860530 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17964540 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11114194 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:11114194 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11114194 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:20634945 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:20042581 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:17964540 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17964540 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20042581 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11114194 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0004184 abnormal baroreceptor physiology IAGP N RGD:5509061 20141003 MGI PMID:15860530 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:16143109 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:20634945 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17964540 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17964540 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:16143109 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:12522242 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:11114194 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0008454 absent retina rod cells IAGP N RGD:5509061 20141003 MGI PMID:11114194 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:20042581 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20042581 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:11114194 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20042581 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:20042581 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17964540 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17964540 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17964540 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:20634945 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17964540 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0011021 abnormal circadian regulation of heart rate IAGP N RGD:5509061 20141003 MGI PMID:17964540 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0011021 abnormal circadian regulation of heart rate IAGP N RGD:5509061 20171012 MGI PMID:15860530 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0011022 abnormal circadian regulation of systemic arterial blood pressure IAGP N RGD:5509061 20171012 MGI PMID:15860530 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:20634945 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:10217146 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:15860530 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0020468 abnormal circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:10217146 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:10217146 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:10518585 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:23471982 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:25288642 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:9822380 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0020471 abnormal circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:10518585 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:10217146 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:10518585 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:11114194 1558359 Cry2 cryptochrome circadian regulator 2 gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20171012 MGI PMID:11114194 1558360 Irag2 inositol 1,4,5-triphosphate receptor associated 2 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20230601 MGI 1558361 Spin4 spindlin family, member 4 gene MP:0001257 increased body length IAGP N RGD:5509061 20240509 MGI PMID:36927955 1558361 Spin4 spindlin family, member 4 gene MP:0001260 increased body weight IAGP N RGD:5509061 20240509 MGI PMID:36927955 1558361 Spin4 spindlin family, member 4 gene MP:0001264 increased body size IAGP N RGD:5509061 20240509 MGI PMID:36927955 1558361 Spin4 spindlin family, member 4 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20240509 MGI PMID:36927955 1558361 Spin4 spindlin family, member 4 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20240509 MGI PMID:36927955 1558361 Spin4 spindlin family, member 4 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20240509 MGI PMID:36927955 1558361 Spin4 spindlin family, member 4 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20240509 MGI PMID:36927955 1558361 Spin4 spindlin family, member 4 gene MP:0004357 long tibia IAGP N RGD:5509061 20240509 MGI PMID:36927955 1558361 Spin4 spindlin family, member 4 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20240509 MGI PMID:36927955 1558361 Spin4 spindlin family, member 4 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20240509 MGI PMID:36927955 1558361 Spin4 spindlin family, member 4 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20240509 MGI PMID:36927955 1558361 Spin4 spindlin family, member 4 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20240509 MGI PMID:36927955 1558361 Spin4 spindlin family, member 4 gene MP:0011692 increased chondrocyte number IAGP N RGD:5509061 20240509 MGI PMID:36927955 1558361 Spin4 spindlin family, member 4 gene MP:0014100 increased chondrocyte proliferation IAGP N RGD:5509061 20240509 MGI PMID:36927955 1558362 Aph1b aph1 homolog B, gamma secretase subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15665098 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16530040 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200130 MGI PMID:30662948 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220811 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20210128 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0002959 increased urine microalbumin level IEA N RGD:5509061 20210520 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220811 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200130 MGI PMID:30662948 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200130 MGI PMID:30662948 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19136662 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20211021 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:18524992 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20220519 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20200130 MGI PMID:30662948 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0008087 decreased T helper 1 cell number IAGP N RGD:5509061 20200130 MGI PMID:30662948 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20200130 MGI PMID:30662948 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20200130 MGI PMID:30662948 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20200130 MGI PMID:30662948 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20200130 MGI PMID:30662948 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20200130 MGI PMID:30662948 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16530040 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20200130 MGI PMID:30662948 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20200130 MGI PMID:30662948 1558365 Vsig4 V-set and immunoglobulin domain containing 4 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20201231 MGI 1558366 Lama4 laminin, alpha 4 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15699217 1558366 Lama4 laminin, alpha 4 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15814800 1558366 Lama4 laminin, alpha 4 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:18794334 1558366 Lama4 laminin, alpha 4 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15699217 1558366 Lama4 laminin, alpha 4 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15814800 1558366 Lama4 laminin, alpha 4 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:18794334 1558366 Lama4 laminin, alpha 4 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:18794334 1558366 Lama4 laminin, alpha 4 gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:15699217 1558366 Lama4 laminin, alpha 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15699217 1558366 Lama4 laminin, alpha 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18794334 1558366 Lama4 laminin, alpha 4 gene MP:0001314 cornea opacity IEA N RGD:5509061 20201231 MGI 1558366 Lama4 laminin, alpha 4 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15814800 1558366 Lama4 laminin, alpha 4 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15699217 1558366 Lama4 laminin, alpha 4 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:15814800 1558366 Lama4 laminin, alpha 4 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0001569 abnormal circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15814800 1558366 Lama4 laminin, alpha 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1558366 Lama4 laminin, alpha 4 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:15699217 1558366 Lama4 laminin, alpha 4 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1558366 Lama4 laminin, alpha 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18794334 1558366 Lama4 laminin, alpha 4 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1558366 Lama4 laminin, alpha 4 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15814800 1558366 Lama4 laminin, alpha 4 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0002833 increased heart weight IEA N RGD:5509061 20181227 MGI 1558366 Lama4 laminin, alpha 4 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1558366 Lama4 laminin, alpha 4 gene MP:0003044 impaired basement membrane formation IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:15814800 1558366 Lama4 laminin, alpha 4 gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:15814800 1558366 Lama4 laminin, alpha 4 gene MP:0003994 abnormal dorsal spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:15814800 1558366 Lama4 laminin, alpha 4 gene MP:0004120 cardiac ischemia IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0004122 abnormal sinus arrhythmia IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0004273 abnormal basal lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:15699217 1558366 Lama4 laminin, alpha 4 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:17344408 1558366 Lama4 laminin, alpha 4 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15699217 1558366 Lama4 laminin, alpha 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1558366 Lama4 laminin, alpha 4 gene MP:0020326 dilated capillary IAGP N RGD:5509061 20160714 MGI PMID:11809810 1558366 Lama4 laminin, alpha 4 gene MP:0020326 dilated capillary IAGP N RGD:5509061 20160714 MGI PMID:16204254 1558366 Lama4 laminin, alpha 4 gene MP:0020452 abnormal axon radial sorting IAGP N RGD:5509061 20170914 MGI PMID:15699217 1558366 Lama4 laminin, alpha 4 gene MP:0020452 abnormal axon radial sorting IAGP N RGD:5509061 20170914 MGI PMID:15814800 1558367 Rab5a RAB5A, member RAS oncogene family gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1558367 Rab5a RAB5A, member RAS oncogene family gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1558367 Rab5a RAB5A, member RAS oncogene family gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1558367 Rab5a RAB5A, member RAS oncogene family gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1558367 Rab5a RAB5A, member RAS oncogene family gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1558367 Rab5a RAB5A, member RAS oncogene family gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1558367 Rab5a RAB5A, member RAS oncogene family gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1558367 Rab5a RAB5A, member RAS oncogene family gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20160421 MGI 1558367 Rab5a RAB5A, member RAS oncogene family gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1558367 Rab5a RAB5A, member RAS oncogene family gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1558367 Rab5a RAB5A, member RAS oncogene family gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20160421 MGI 1558368 Eefsec eukaryotic elongation factor, selenocysteine-tRNA-specific gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1558368 Eefsec eukaryotic elongation factor, selenocysteine-tRNA-specific gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160421 MGI 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210128 MGI 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20160421 MGI 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20231207 MGI 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20151210 MGI PMID:23590306 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23684610 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:23684610 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20151210 MGI PMID:23590306 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:23684610 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20151210 MGI PMID:23590306 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:23922714 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23684610 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20151210 MGI PMID:23590306 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:23922714 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20151210 MGI PMID:23590306 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23684610 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20160421 MGI 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20160421 MGI 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23684610 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20240704 MGI PMID:23684610 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20141003 MGI PMID:23684610 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0004781 abnormal surfactant composition IAGP N RGD:5509061 20151210 MGI PMID:23590306 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20141003 MGI PMID:23684610 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20151210 MGI PMID:23590306 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160421 MGI 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:23922714 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0005426 tachypnea IAGP N RGD:5509061 20151210 MGI PMID:23590306 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20151112 MGI 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20160421 MGI 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:23922714 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:23922714 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20151210 MGI PMID:23590306 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0010052 increased grip strength IEA N RGD:5509061 20160421 MGI 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:23922714 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0010891 increased alveolar lamellar body number IAGP N RGD:5509061 20141003 MGI PMID:23684610 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0010992 increased surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:23684610 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0010992 increased surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:23922714 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0010992 increased surfactant secretion IAGP N RGD:5509061 20151210 MGI PMID:23590306 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0010998 pulmonary alveolar proteinosis IAGP N RGD:5509061 20141003 MGI PMID:23684610 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1558369 Adgrf5 adhesion G protein-coupled receptor F5 gene MP:0031632 increased lung cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:23684610 1558370 Flna filamin, alpha gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0000771 abnormal brain size IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11929848 1558370 Flna filamin, alpha gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1558370 Flna filamin, alpha gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:11929848 1558370 Flna filamin, alpha gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0010432 common ventricle IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0010620 thick mitral valve IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11929848 1558370 Flna filamin, alpha gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16825286 1558370 Flna filamin, alpha gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558370 Flna filamin, alpha gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17172441 1558372 Cd300a CD300A molecule gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22826299 1558372 Cd300a CD300A molecule gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210128 MGI 1558372 Cd300a CD300A molecule gene MP:0001406 abnormal gait IEA N RGD:5509061 20210128 MGI 1558372 Cd300a CD300A molecule gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22826299 1558372 Cd300a CD300A molecule gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 1558372 Cd300a CD300A molecule gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20210128 MGI 1558372 Cd300a CD300A molecule gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22826299 1558372 Cd300a CD300A molecule gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22826299 1558372 Cd300a CD300A molecule gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:22826299 1558372 Cd300a CD300A molecule gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:22826299 1558372 Cd300a CD300A molecule gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:22826299 1558372 Cd300a CD300A molecule gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22826299 1558372 Cd300a CD300A molecule gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1558373 Cfap68 cilia and flagella associated protein 68 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240627 MGI PMID:38835510 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20200310 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200310 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200310 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20200310 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20200310 MGI PMID:27840305 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:27840305 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20200310 MGI PMID:24896341 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20200310 MGI PMID:27840305 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200310 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200310 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0005439 decreased glycogen level IAGP N RGD:5509061 20200310 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20200310 MGI PMID:27840305 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:28508477 1558375 Creg1 cellular repressor of E1A-stimulated genes 1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:27840305 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18448090 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:18448090 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:19056886 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:19056886 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:18448090 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18448090 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19056886 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0003044 impaired basement membrane formation IAGP N RGD:5509061 20141003 MGI PMID:21350012 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:18448090 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:21673655 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19056886 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:19056886 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:19056886 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:18448090 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:19056886 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18448090 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:19056886 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0008533 abnormal anterior visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:19056886 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19056886 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18448090 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19056886 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21350012 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:18448090 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0013283 failure of ventral body wall closure IAGP N RGD:5509061 20141003 MGI PMID:18448090 1558376 Flrt3 fibronectin leucine rich transmembrane protein 3 gene MP:0013283 failure of ventral body wall closure IAGP N RGD:5509061 20141003 MGI PMID:19056886 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15109498 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11113183 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12765942 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11113183 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11113183 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23742761 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12765942 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:12765942 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:21119595 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:23742761 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:11113183 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12765942 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:24416220 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:23742761 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:24416220 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:15109498 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:23742761 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21119595 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15109498 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0003932 abnormal molar crown morphology IAGP N RGD:5509061 20141003 MGI PMID:24416220 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:15109498 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20141003 MGI PMID:24416220 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20141003 MGI PMID:15109498 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0004380 short frontal bone IAGP N RGD:5509061 20141003 MGI PMID:24416220 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:15109498 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20141003 MGI PMID:15109498 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:15109498 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:15109498 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:15109498 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12765942 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12765942 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12765942 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12765942 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15109498 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:23742761 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:23742761 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20191226 MGI PMID:11113183 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:15109498 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23742761 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0011165 abnormal tooth root development IAGP N RGD:5509061 20141003 MGI PMID:24416220 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0011274 short excitatory postsynaptic current decay time IAGP N RGD:5509061 20141003 MGI PMID:23742761 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20141003 MGI PMID:24416220 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20180301 MGI PMID:23742761 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:15109498 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0030388 large fontanelles IAGP N RGD:5509061 20171207 MGI PMID:15109498 1558377 Rps6ka3 ribosomal protein S6 kinase polypeptide 3 gene MP:0030536 abnormal diastema morphology IAGP N RGD:5509061 20180201 MGI PMID:24416220 1558378 St6galnac1 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20230622 MGI PMID:35303419 1558378 St6galnac1 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20230622 MGI PMID:35303419 1558378 St6galnac1 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20230622 MGI PMID:35303419 1558378 St6galnac1 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 gene MP:0014030 abnormal mucous gland physiology IAGP N RGD:5509061 20230622 MGI PMID:35303419 1558378 St6galnac1 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 gene MP:0014219 decreased intestinal mucosa thickness IAGP N RGD:5509061 20230622 MGI PMID:35303419 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20181220 MGI PMID:22527485 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000126 brittle teeth IAGP N RGD:5509061 20181220 MGI PMID:22527485 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20181220 MGI PMID:22527485 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20181220 MGI PMID:22527485 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20181227 MGI 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20181220 MGI PMID:22527485 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20181220 MGI PMID:22527485 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0004791 absent lower incisors IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0008862 asymmetric snout IAGP N RGD:5509061 20171019 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0009524 absent submandibular gland IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0009880 decreased mouth size IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0009917 abnormal hyoid bone body morphology IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16960803 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0020301 short tongue IAGP N RGD:5509061 20221027 MGI PMID:16751105 1558379 Satb2 special AT-rich sequence binding protein 2 gene MP:0030868 absent thyroid cartilage IAGP N RGD:5509061 20181101 MGI PMID:16751105 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0004235 abnormal masseter muscle morphology IAGP N RGD:5509061 20171214 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0012091 increased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0012263 decreased hindbrain size IAGP N RGD:5509061 20141003 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20171214 MGI PMID:23935987 1558380 Pak1ip1 PAK1 interacting protein 1 gene MP:0030197 small nasal septum IAGP N RGD:5509061 20171012 MGI PMID:23935987 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:7845467 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0000589 thin tail IEA N RGD:5509061 20111116 MGI 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:14499111 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001224 abnormal keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001262 decreased body weight IEA N RGD:5509061 20111116 MGI 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001577 anemia IEA N RGD:5509061 20111116 MGI 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:9164938 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:9164938 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:7845467 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12810685 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:7845467 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001868 ovary inflammation IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002138 abnormal hepatobiliary system morphology IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21419662 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9164938 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:9164938 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:9164938 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9164938 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9164938 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:9164938 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12810685 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0003046 liver cirrhosis IEA N RGD:5509061 20111116 MGI 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0003325 decreased liver function IEA N RGD:5509061 20111116 MGI 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0003326 liver failure IEA N RGD:5509061 20111116 MGI 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0003596 epididymis inflammation IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0003711 pathological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9164938 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9164938 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0005416 abnormal circulating protein level IEA N RGD:5509061 20111116 MGI 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20111116 MGI 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:7845467 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20111116 MGI 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12810685 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:12810685 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:14499111 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:12810685 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12810685 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008343 abnormal gamma-delta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21419662 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:12810685 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:12810685 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:21419662 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:9164938 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:9164938 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:9164938 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:9164938 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20111116 MGI 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0010861 increased respiratory mucosa goblet cell number IAGP N RGD:5509061 20141003 MGI PMID:10940923 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0010909 pulmonary alveolar hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7834753 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0011083 lethality at weaning, complete penetrance IEA N RGD:5509061 20111116 MGI 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0013587 absent thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:1443055 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0013587 absent thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:7845467 1558382 Relb avian reticuloendotheliosis viral (v-rel) oncogene related B gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:9164938 1558384 Ergic1 endoplasmic reticulum-golgi intermediate compartment 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1558384 Ergic1 endoplasmic reticulum-golgi intermediate compartment 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1558385 Lrch2 leucine-rich repeats and calponin homology (CH) domain containing 2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1558385 Lrch2 leucine-rich repeats and calponin homology (CH) domain containing 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1558385 Lrch2 leucine-rich repeats and calponin homology (CH) domain containing 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1558388 E4f1 E4F transcription factor 1 gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0001234 absent suprabasal layer IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15226446 1558388 E4f1 E4F transcription factor 1 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:15226446 1558388 E4f1 E4F transcription factor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15226446 1558388 E4f1 E4F transcription factor 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:15226446 1558388 E4f1 E4F transcription factor 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0009560 absent epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0009759 abnormal hair follicle bulge morphology IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21088222 1558388 E4f1 E4F transcription factor 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15226446 1558389 Epha4 Eph receptor A4 gene MP:0000860 abnormal primary somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17035292 1558389 Epha4 Eph receptor A4 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200507 MGI PMID:28346224 1558389 Epha4 Eph receptor A4 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12649481 1558389 Epha4 Eph receptor A4 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20150219 MGI PMID:24623763 1558389 Epha4 Eph receptor A4 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:16600854 1558389 Epha4 Eph receptor A4 gene MP:0001070 abnormal abducens nerve morphology IAGP N RGD:5509061 20200507 MGI PMID:28346224 1558389 Epha4 Eph receptor A4 gene MP:0001386 abnormal maternal nurturing IEA N RGD:5509061 20111116 MGI 1558389 Epha4 Eph receptor A4 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20111215 MGI 1558389 Epha4 Eph receptor A4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11182082 1558389 Epha4 Eph receptor A4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11242070 1558389 Epha4 Eph receptor A4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11431694 1558389 Epha4 Eph receptor A4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12649481 1558389 Epha4 Eph receptor A4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:14699416 1558389 Epha4 Eph receptor A4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16102535 1558389 Epha4 Eph receptor A4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17785183 1558389 Epha4 Eph receptor A4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19734893 1558389 Epha4 Eph receptor A4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20014422 1558389 Epha4 Eph receptor A4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9789074 1558389 Epha4 Eph receptor A4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20150219 MGI PMID:24623763 1558389 Epha4 Eph receptor A4 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:14699416 1558389 Epha4 Eph receptor A4 gene MP:0001513 limb grasping IEA N RGD:5509061 20111116 MGI 1558389 Epha4 Eph receptor A4 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:9789074 1558389 Epha4 Eph receptor A4 gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:9789074 1558389 Epha4 Eph receptor A4 gene MP:0001922 reduced male fertility IEA N RGD:5509061 20111116 MGI 1558389 Epha4 Eph receptor A4 gene MP:0001935 decreased litter size IEA N RGD:5509061 20111116 MGI 1558389 Epha4 Eph receptor A4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11182082 1558389 Epha4 Eph receptor A4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20014422 1558389 Epha4 Eph receptor A4 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:17035292 1558389 Epha4 Eph receptor A4 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:9789074 1558389 Epha4 Eph receptor A4 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20200507 MGI PMID:28346224 1558389 Epha4 Eph receptor A4 gene MP:0002286 cryptorchism IEA N RGD:5509061 20111116 MGI 1558389 Epha4 Eph receptor A4 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:11182082 1558389 Epha4 Eph receptor A4 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:11242070 1558389 Epha4 Eph receptor A4 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:12649481 1558389 Epha4 Eph receptor A4 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:14699416 1558389 Epha4 Eph receptor A4 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:9789074 1558389 Epha4 Eph receptor A4 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20150219 MGI PMID:24623763 1558389 Epha4 Eph receptor A4 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:11242070 1558389 Epha4 Eph receptor A4 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:11431694 1558389 Epha4 Eph receptor A4 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:16600854 1558389 Epha4 Eph receptor A4 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20190815 MGI PMID:27373307 1558389 Epha4 Eph receptor A4 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:9789074 1558389 Epha4 Eph receptor A4 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20150219 MGI PMID:24623763 1558389 Epha4 Eph receptor A4 gene MP:0003880 abnormal central pattern generator function IAGP N RGD:5509061 20141003 MGI PMID:12649481 1558389 Epha4 Eph receptor A4 gene MP:0003880 abnormal central pattern generator function IAGP N RGD:5509061 20141003 MGI PMID:16102535 1558389 Epha4 Eph receptor A4 gene MP:0003989 abnormal barrel cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17035292 1558389 Epha4 Eph receptor A4 gene MP:0004100 abnormal spinal cord interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17785183 1558389 Epha4 Eph receptor A4 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19734893 1558389 Epha4 Eph receptor A4 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19182796 1558389 Epha4 Eph receptor A4 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:11182082 1558389 Epha4 Eph receptor A4 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:11242070 1558389 Epha4 Eph receptor A4 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16102535 1558389 Epha4 Eph receptor A4 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:19734893 1558389 Epha4 Eph receptor A4 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:9789074 1558389 Epha4 Eph receptor A4 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20200507 MGI PMID:28346224 1558389 Epha4 Eph receptor A4 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:16102535 1558389 Epha4 Eph receptor A4 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:17785183 1558389 Epha4 Eph receptor A4 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:19734893 1558389 Epha4 Eph receptor A4 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:9789074 1558389 Epha4 Eph receptor A4 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20150219 MGI PMID:24623763 1558389 Epha4 Eph receptor A4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20111116 MGI 1558389 Epha4 Eph receptor A4 gene MP:0010859 abnormal anterior commissure pars anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:11182082 1558389 Epha4 Eph receptor A4 gene MP:0010859 abnormal anterior commissure pars anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:16102535 1558389 Epha4 Eph receptor A4 gene MP:0010860 abnormal anterior commissure pars posterior morphology IAGP N RGD:5509061 20141003 MGI PMID:11182082 1558389 Epha4 Eph receptor A4 gene MP:0010860 abnormal anterior commissure pars posterior morphology IAGP N RGD:5509061 20141003 MGI PMID:16102535 1558389 Epha4 Eph receptor A4 gene MP:0020529 ectopic thalamus IAGP N RGD:5509061 20180208 MGI PMID:16102535 1558392 Zpbp2 zona pellucida binding protein 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17664285 1558392 Zpbp2 zona pellucida binding protein 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17664285 1558392 Zpbp2 zona pellucida binding protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17664285 1558392 Zpbp2 zona pellucida binding protein 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17664285 1558392 Zpbp2 zona pellucida binding protein 2 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17664285 1558392 Zpbp2 zona pellucida binding protein 2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17664285 1558392 Zpbp2 zona pellucida binding protein 2 gene MP:0005411 delayed fertilization IAGP N RGD:5509061 20141003 MGI PMID:17664285 1558392 Zpbp2 zona pellucida binding protein 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17664285 1558392 Zpbp2 zona pellucida binding protein 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17664285 1558392 Zpbp2 zona pellucida binding protein 2 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20141003 MGI PMID:17664285 1558392 Zpbp2 zona pellucida binding protein 2 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17664285 1558392 Zpbp2 zona pellucida binding protein 2 gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:17664285 1558392 Zpbp2 zona pellucida binding protein 2 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17664285 1558392 Zpbp2 zona pellucida binding protein 2 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:17664285 1558392 Zpbp2 zona pellucida binding protein 2 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:17664285 1558393 Sp2 Sp2 transcription factor gene MP:0000929 open neural tube IAGP N RGD:5509061 20141225 MGI PMID:20221402 1558393 Sp2 Sp2 transcription factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23293287 1558393 Sp2 Sp2 transcription factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20221402 1558393 Sp2 Sp2 transcription factor gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141225 MGI PMID:20221402 1558393 Sp2 Sp2 transcription factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23293287 1558393 Sp2 Sp2 transcription factor gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23293287 1558393 Sp2 Sp2 transcription factor gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20221402 1558393 Sp2 Sp2 transcription factor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23293287 1558393 Sp2 Sp2 transcription factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20221402 1558393 Sp2 Sp2 transcription factor gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:23293287 1558393 Sp2 Sp2 transcription factor gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:23293287 1558393 Sp2 Sp2 transcription factor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20221402 1558393 Sp2 Sp2 transcription factor gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:20221402 1558393 Sp2 Sp2 transcription factor gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20221402 1558393 Sp2 Sp2 transcription factor gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:23293287 1558393 Sp2 Sp2 transcription factor gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:23293287 1558393 Sp2 Sp2 transcription factor gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:23293287 1558393 Sp2 Sp2 transcription factor gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:23293287 1558393 Sp2 Sp2 transcription factor gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:23293287 1558393 Sp2 Sp2 transcription factor gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:23293287 1558393 Sp2 Sp2 transcription factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20221402 1558393 Sp2 Sp2 transcription factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23293287 1558393 Sp2 Sp2 transcription factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20221402 1558393 Sp2 Sp2 transcription factor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23293287 1558393 Sp2 Sp2 transcription factor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20221402 1558393 Sp2 Sp2 transcription factor gene MP:0011705 absent fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20221402 1558393 Sp2 Sp2 transcription factor gene MP:0020083 decreased hippocampus volume IAGP N RGD:5509061 20170706 MGI PMID:23293287 1558393 Sp2 Sp2 transcription factor gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20170706 MGI PMID:23293287 1558399 Cbx4 chromobox 4 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:23362346 1558399 Cbx4 chromobox 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1558399 Cbx4 chromobox 4 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1558399 Cbx4 chromobox 4 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23362346 1558399 Cbx4 chromobox 4 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23362346 1558399 Cbx4 chromobox 4 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:23362346 1558399 Cbx4 chromobox 4 gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:23362346 1558399 Cbx4 chromobox 4 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160421 MGI 1558399 Cbx4 chromobox 4 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23362346 1558399 Cbx4 chromobox 4 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23362346 1558399 Cbx4 chromobox 4 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1558399 Cbx4 chromobox 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23362346 1558399 Cbx4 chromobox 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0000111 cleft palate IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0000192 abnormal mineral level IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0003717 pallor IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20240523 MGI 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0004265 abnormal placental transport IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0005262 coloboma IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0008274 failure of bone ossification IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0010714 iris coloboma IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0013848 subcutaneous edema IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558400 Slc13a4 solute carrier family 13 (sodium/sulfate symporters), member 4 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20170518 MGI PMID:26292834 1558401 Zfp365 zinc finger protein 365 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141030 MGI PMID:24481677 1558401 Zfp365 zinc finger protein 365 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23912123 1558401 Zfp365 zinc finger protein 365 gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20141030 MGI PMID:24481677 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:11181696 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11181696 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11181696 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12055243 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11181696 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16361315 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0003134 increased late pro-B cell number IAGP N RGD:5509061 20240404 MGI PMID:12055243 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12055243 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0005022 abnormal immature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11181696 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:11181696 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:12055243 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11181696 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12055243 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16361315 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11181696 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12055243 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16361315 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12055243 1558402 Vpreb1b V-set pre-B cell surrogate light chain 1B gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:11181696 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20181108 MGI PMID:29349289 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20170622 MGI PMID:21964919 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20181108 MGI PMID:29349289 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20170622 MGI PMID:21964919 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20170622 MGI PMID:26515654 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20181108 MGI PMID:29349289 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20181108 MGI PMID:29349289 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20170622 MGI PMID:21964919 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20170622 MGI PMID:26515654 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20181108 MGI PMID:29349289 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20181108 MGI PMID:29349289 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20170622 MGI PMID:26515654 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0001393 ataxia IAGP N RGD:5509061 20170622 MGI PMID:26515654 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170622 MGI PMID:21964919 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170622 MGI PMID:26515654 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20170622 MGI PMID:21964919 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0002183 gliosis IAGP N RGD:5509061 20170622 MGI PMID:26515654 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20170622 MGI PMID:21964919 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20170622 MGI PMID:21964919 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20111116 MGI 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20181108 MGI PMID:29349289 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20170622 MGI PMID:21964919 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20181108 MGI PMID:29349289 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20170622 MGI PMID:26515654 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0008269 abnormal hippocampus CA4 region morphology IAGP N RGD:5509061 20170622 MGI PMID:26515654 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20170622 MGI PMID:26515654 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20181108 MGI PMID:29349289 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0008918 microgliosis IAGP N RGD:5509061 20181108 MGI PMID:29349289 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170622 MGI PMID:21964919 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20181108 MGI PMID:29349289 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0012779 abnormal brain cholesterol level IAGP N RGD:5509061 20170622 MGI PMID:21964919 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:21964919 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:21964919 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:26515654 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0031561 increased ganglioside level IAGP N RGD:5509061 20240704 MGI PMID:21964919 1558403 Slc9a6 solute carrier family 9 (sodium/hydrogen exchanger), member 6 gene MP:0031561 increased ganglioside level IAGP N RGD:5509061 20240704 MGI PMID:26515654 1558404 Zdhhc14 zinc finger, DHHC domain containing 14 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1558404 Zdhhc14 zinc finger, DHHC domain containing 14 gene MP:0001147 small testis IEA N RGD:5509061 20230119 MGI 1558404 Zdhhc14 zinc finger, DHHC domain containing 14 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1558404 Zdhhc14 zinc finger, DHHC domain containing 14 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1558404 Zdhhc14 zinc finger, DHHC domain containing 14 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1558404 Zdhhc14 zinc finger, DHHC domain containing 14 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1558407 Hecw1 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1 gene MP:0000745 tremors IEA N RGD:5509061 20181227 MGI 1558407 Hecw1 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1558407 Hecw1 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20181227 MGI 1558407 Hecw1 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1 gene MP:0001523 impaired righting response IEA N RGD:5509061 20220811 MGI 1558407 Hecw1 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1558407 Hecw1 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20210506 MGI PMID:33633267 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20210506 MGI PMID:33633267 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0001925 male infertility IAGP N RGD:5509061 20210506 MGI PMID:33633267 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20210506 MGI PMID:33633267 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210506 MGI PMID:33633267 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210506 MGI PMID:33633267 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210506 MGI PMID:33633267 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210506 MGI PMID:33633267 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230601 MGI 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20240523 MGI 1558408 Rimklb ribosomal modification protein rimK-like family member B gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20160421 MGI 1558410 Fam83d family with sequence similarity 83, member D gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1558410 Fam83d family with sequence similarity 83, member D gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1558410 Fam83d family with sequence similarity 83, member D gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 1558410 Fam83d family with sequence similarity 83, member D gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 1558410 Fam83d family with sequence similarity 83, member D gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1558410 Fam83d family with sequence similarity 83, member D gene MP:0001148 enlarged testis IEA N RGD:5509061 20210826 MGI 1558410 Fam83d family with sequence similarity 83, member D gene MP:0001293 anophthalmia IEA N RGD:5509061 20210826 MGI 1558410 Fam83d family with sequence similarity 83, member D gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220519 MGI 1558410 Fam83d family with sequence similarity 83, member D gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1558410 Fam83d family with sequence similarity 83, member D gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1558410 Fam83d family with sequence similarity 83, member D gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1558410 Fam83d family with sequence similarity 83, member D gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220519 MGI 1558410 Fam83d family with sequence similarity 83, member D gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220519 MGI 1558410 Fam83d family with sequence similarity 83, member D gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220519 MGI 1558412 Zfp830 zinc finger protein 830 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21191184 1558412 Zfp830 zinc finger protein 830 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210128 MGI 1558412 Zfp830 zinc finger protein 830 gene MP:0001406 abnormal gait IEA N RGD:5509061 20210128 MGI 1558412 Zfp830 zinc finger protein 830 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:15988037 1558412 Zfp830 zinc finger protein 830 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21191184 1558412 Zfp830 zinc finger protein 830 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:15988037 1558412 Zfp830 zinc finger protein 830 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15988037 1558412 Zfp830 zinc finger protein 830 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:15988037 1558412 Zfp830 zinc finger protein 830 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15988037 1558412 Zfp830 zinc finger protein 830 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21191184 1558412 Zfp830 zinc finger protein 830 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15988037 1558412 Zfp830 zinc finger protein 830 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21191184 1558412 Zfp830 zinc finger protein 830 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558412 Zfp830 zinc finger protein 830 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:15988037 1558412 Zfp830 zinc finger protein 830 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:15988037 1558412 Zfp830 zinc finger protein 830 gene MP:0012118 absent trophectoderm cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15988037 1558412 Zfp830 zinc finger protein 830 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20200402 MGI 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20190502 MGI 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0001438 aphagia IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0001577 anemia IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0003717 pallor IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0004573 absent limb buds IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0004793 abnormal synaptic vesicle clustering IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0009328 delayed heart looping IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0011733 fused somites IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558414 Eps15l1 epidermal growth factor receptor pathway substrate 15-like 1 gene MP:0030951 abnormal endocytosis IAGP N RGD:5509061 20210318 MGI PMID:30692166 1558415 Sap30bp SAP30 binding protein gene MP:0001577 anemia IEA N RGD:5509061 20111116 MGI 1558416 Naa38 N(alpha)-acetyltransferase 38, NatC auxiliary subunit gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1558416 Naa38 N(alpha)-acetyltransferase 38, NatC auxiliary subunit gene MP:0000274 enlarged heart IEA N RGD:5509061 20201022 MGI 1558416 Naa38 N(alpha)-acetyltransferase 38, NatC auxiliary subunit gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20201022 MGI 1558416 Naa38 N(alpha)-acetyltransferase 38, NatC auxiliary subunit gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20200514 MGI 1558416 Naa38 N(alpha)-acetyltransferase 38, NatC auxiliary subunit gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20200514 MGI 1558416 Naa38 N(alpha)-acetyltransferase 38, NatC auxiliary subunit gene MP:0000709 enlarged thymus IEA N RGD:5509061 20200514 MGI 1558416 Naa38 N(alpha)-acetyltransferase 38, NatC auxiliary subunit gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20200514 MGI 1558416 Naa38 N(alpha)-acetyltransferase 38, NatC auxiliary subunit gene MP:0001262 decreased body weight IEA N RGD:5509061 20210128 MGI 1558416 Naa38 N(alpha)-acetyltransferase 38, NatC auxiliary subunit gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20200514 MGI 1558416 Naa38 N(alpha)-acetyltransferase 38, NatC auxiliary subunit gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20201022 MGI 1558416 Naa38 N(alpha)-acetyltransferase 38, NatC auxiliary subunit gene MP:0009709 hydrometra IEA N RGD:5509061 20200514 MGI 1558416 Naa38 N(alpha)-acetyltransferase 38, NatC auxiliary subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558416 Naa38 N(alpha)-acetyltransferase 38, NatC auxiliary subunit gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1558417 Poln DNA polymerase N gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20170713 MGI PMID:28570559 1558417 Poln DNA polymerase N gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20170713 MGI PMID:28570559 1558417 Poln DNA polymerase N gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170713 MGI PMID:28570559 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0000562 polydactyly IEA N RGD:5509061 20160804 MGI 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0001147 small testis IAGP N RGD:5509061 20201029 MGI PMID:31242413 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0001147 small testis IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0001756 abnormal urination IEA N RGD:5509061 20160804 MGI 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0001925 male infertility IAGP N RGD:5509061 20201015 MGI PMID:32345962 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0001925 male infertility IAGP N RGD:5509061 20201029 MGI PMID:31242413 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20160804 MGI 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0005159 azoospermia IAGP N RGD:5509061 20201029 MGI PMID:31242413 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0005159 azoospermia IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20201029 MGI PMID:31242413 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20160804 MGI 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160804 MGI 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20201029 MGI PMID:31242413 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20201029 MGI PMID:31242413 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20201015 MGI PMID:32345962 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20201029 MGI PMID:31242413 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558419 Hsf2bp heat shock transcription factor 2 binding protein gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220616 MGI PMID:32845237 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20210114 MGI PMID:32217665 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20210114 MGI PMID:32217665 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20210114 MGI PMID:32217665 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0001258 decreased body length IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210114 MGI PMID:32217665 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0001304 cataract IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20210114 MGI PMID:32217665 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0001925 male infertility IAGP N RGD:5509061 20210114 MGI PMID:32217665 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0002608 increased hematocrit IEA N RGD:5509061 20220811 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20210114 MGI PMID:32217665 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20210114 MGI PMID:32217665 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0004222 iris synechia IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0004952 increased spleen weight IEA N RGD:5509061 20220519 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20220811 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20210114 MGI PMID:32217665 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0010052 increased grip strength IEA N RGD:5509061 20210826 MGI 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20210114 MGI PMID:32217665 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210114 MGI PMID:32217665 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20210114 MGI PMID:32217665 1558420 Mettl5 methyltransferase 5, N6-adenosine gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20230518 MGI PMID:35416977 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220811 MGI 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0000599 enlarged liver IEA N RGD:5509061 20220811 MGI 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20231207 MGI PMID:32619424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23499424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230518 MGI PMID:35416977 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20190502 MGI 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20231207 MGI PMID:32619424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20231207 MGI PMID:32619424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20231207 MGI PMID:32619424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:23499424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20230518 MGI PMID:35416977 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20220811 MGI 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23499424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23499424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20201022 MGI 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:23499424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:23499424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23499424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:23499424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23499424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0009130 increased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:23499424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23499424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23499424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23499424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20190502 MGI 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23499424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20230518 MGI PMID:35416977 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0010274 increased organ/body region tumor incidence IAGP N RGD:5509061 20231207 MGI PMID:32619424 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20230518 MGI PMID:35416977 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20230518 MGI PMID:35416977 1558421 Tbl1xr1 transducin (beta)-like 1X-linked receptor 1 gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:23499424 1558423 Dnajb12 DnaJ heat shock protein family (Hsp40) member B12 gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20210826 MGI 1558423 Dnajb12 DnaJ heat shock protein family (Hsp40) member B12 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20220519 MGI 1558423 Dnajb12 DnaJ heat shock protein family (Hsp40) member B12 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1558423 Dnajb12 DnaJ heat shock protein family (Hsp40) member B12 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558423 Dnajb12 DnaJ heat shock protein family (Hsp40) member B12 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20160421 MGI 1558424 Fggy FGGY carbohydrate kinase domain containing gene MP:0004609 vertebral fusion IEA N RGD:5509061 20201231 MGI 1558425 Tlr13 toll-like receptor 13 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1558425 Tlr13 toll-like receptor 13 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20211021 MGI 1558426 Ric8b RIC8 guanine nucleotide exchange factor B gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1558426 Ric8b RIC8 guanine nucleotide exchange factor B gene MP:0001314 cornea opacity IEA N RGD:5509061 20201231 MGI 1558426 Ric8b RIC8 guanine nucleotide exchange factor B gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1558426 Ric8b RIC8 guanine nucleotide exchange factor B gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20180322 MGI PMID:29118104 1558426 Ric8b RIC8 guanine nucleotide exchange factor B gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20180322 MGI PMID:29118104 1558426 Ric8b RIC8 guanine nucleotide exchange factor B gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1558426 Ric8b RIC8 guanine nucleotide exchange factor B gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20180322 MGI PMID:29118104 1558426 Ric8b RIC8 guanine nucleotide exchange factor B gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20180322 MGI PMID:29118104 1558426 Ric8b RIC8 guanine nucleotide exchange factor B gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20180322 MGI PMID:29118104 1558426 Ric8b RIC8 guanine nucleotide exchange factor B gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20180322 MGI PMID:29118104 1558426 Ric8b RIC8 guanine nucleotide exchange factor B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180322 MGI PMID:29118104 1558426 Ric8b RIC8 guanine nucleotide exchange factor B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558426 Ric8b RIC8 guanine nucleotide exchange factor B gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20180322 MGI PMID:29118104 1558426 Ric8b RIC8 guanine nucleotide exchange factor B gene MP:0012020 abnormal olfactory epithelium physiology IAGP N RGD:5509061 20180322 MGI PMID:29118104 1558426 Ric8b RIC8 guanine nucleotide exchange factor B gene MP:0020348 decreased olfactory sensory neuron number IAGP N RGD:5509061 20180322 MGI PMID:29118104 1558427 Taar8b trace amine-associated receptor 8B gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1558427 Taar8b trace amine-associated receptor 8B gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1558427 Taar8b trace amine-associated receptor 8B gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1558427 Taar8b trace amine-associated receptor 8B gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1558427 Taar8b trace amine-associated receptor 8B gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20220811 MGI 1558427 Taar8b trace amine-associated receptor 8B gene MP:0001304 cataract IEA N RGD:5509061 20221215 MGI 1558427 Taar8b trace amine-associated receptor 8B gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1558427 Taar8b trace amine-associated receptor 8B gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1558427 Taar8b trace amine-associated receptor 8B gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20221215 MGI 1558427 Taar8b trace amine-associated receptor 8B gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210805 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210805 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210805 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210805 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0002175 decreased brain weight IEA N RGD:5509061 20210805 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210805 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0003402 decreased liver weight IEA N RGD:5509061 20220519 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210805 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210805 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20210805 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0009312 increased jejunum adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210805 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210805 MGI 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0010138 arteritis IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558429 Ssbp2 single-stranded DNA binding protein 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20348955 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170504 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0003266 biliary cyst IEA N RGD:5509061 20170504 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0010484 bicuspid aortic valve IEA N RGD:5509061 20170504 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0010602 abnormal pulmonary valve cusp morphology IEA N RGD:5509061 20170504 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0013875 increased trigeminal neuroma incidence IEA N RGD:5509061 20170504 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0013968 multiple persisting craniopharyngeal ducts IEA N RGD:5509061 20170504 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0013973 abnormal hepatic vein connection IEA N RGD:5509061 20170504 MGI 1558430 Capza2 capping actin protein of muscle Z-line subunit alpha 2 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1558431 Rhox13 reproductive homeobox 13 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20170622 MGI PMID:27486269 1558431 Rhox13 reproductive homeobox 13 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20170622 MGI PMID:27486269 1558431 Rhox13 reproductive homeobox 13 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20170622 MGI PMID:27486269 1558431 Rhox13 reproductive homeobox 13 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20170622 MGI PMID:27486269 1558431 Rhox13 reproductive homeobox 13 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20170622 MGI PMID:27486269 1558432 Lysmd1 LysM, putative peptidoglycan-binding, domain containing 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210826 MGI 1558432 Lysmd1 LysM, putative peptidoglycan-binding, domain containing 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1558433 Sik2 salt inducible kinase 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1558433 Sik2 salt inducible kinase 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20160505 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20160505 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160505 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20160505 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20160505 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20160505 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0005409 darkened coat color IAGP N RGD:5509061 20150129 MGI PMID:20819186 1558433 Sik2 salt inducible kinase 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20160505 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20160505 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20160505 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20160505 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20160505 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20160505 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20160505 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0030022 decreased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:24898145 1558433 Sik2 salt inducible kinase 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:24898145 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:12897243 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0000794 abnormal parietal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0000798 abnormal frontal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:12897243 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:12897243 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:18324732 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:12897243 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:12897243 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:18324732 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:12897243 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:18324732 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17977657 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:12897243 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12897243 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12897243 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0002316 anoxia IAGP N RGD:5509061 20141003 MGI PMID:12897243 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:12897243 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0003005 abnormal hippocampal fimbria morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18324732 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0004267 abnormal optic tract morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0008219 abnormal dorsal telencephalic commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:17977657 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0008440 abnormal subplate morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:18324732 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0010859 abnormal anterior commissure pars anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0010860 abnormal anterior commissure pars posterior morphology IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17977657 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17977657 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18324732 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17977657 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12897243 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0020546 increased hippocampal fornix size IAGP N RGD:5509061 20180301 MGI PMID:15572149 1558435 Mapk8ip3 mitogen-activated protein kinase 8 interacting protein 3 gene MP:0020549 increased optic chiasm size IAGP N RGD:5509061 20180301 MGI PMID:15572149 1558436 Ccdc40 coiled-coil domain containing 40 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1558436 Ccdc40 coiled-coil domain containing 40 gene MP:0000542 left-sided isomerism IAGP N RGD:5509061 20141003 MGI PMID:21131974 1558436 Ccdc40 coiled-coil domain containing 40 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21131974 1558436 Ccdc40 coiled-coil domain containing 40 gene MP:0001925 male infertility IEA N RGD:5509061 20220811 MGI 1558436 Ccdc40 coiled-coil domain containing 40 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:21131974 1558436 Ccdc40 coiled-coil domain containing 40 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1558436 Ccdc40 coiled-coil domain containing 40 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:21131974 1558436 Ccdc40 coiled-coil domain containing 40 gene MP:0004131 abnormal motile primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:21131974 1558436 Ccdc40 coiled-coil domain containing 40 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:21131974 1558436 Ccdc40 coiled-coil domain containing 40 gene MP:0010854 lung situs inversus IAGP N RGD:5509061 20141003 MGI PMID:21131974 1558436 Ccdc40 coiled-coil domain containing 40 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21131974 1558437 Prss33 serine protease 33 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1558437 Prss33 serine protease 33 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1558437 Prss33 serine protease 33 gene MP:0000692 small spleen IEA N RGD:5509061 20220519 MGI 1558437 Prss33 serine protease 33 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220519 MGI 1558437 Prss33 serine protease 33 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220519 MGI 1558437 Prss33 serine protease 33 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220519 MGI 1558437 Prss33 serine protease 33 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220519 MGI 1558437 Prss33 serine protease 33 gene MP:0001147 small testis IEA N RGD:5509061 20220519 MGI 1558437 Prss33 serine protease 33 gene MP:0001262 decreased body weight IEA N RGD:5509061 20220519 MGI 1558437 Prss33 serine protease 33 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1558437 Prss33 serine protease 33 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20220519 MGI 1558437 Prss33 serine protease 33 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20220519 MGI 1558440 Prmt8 protein arginine N-methyltransferase 8 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20161124 MGI PMID:26665171 1558440 Prmt8 protein arginine N-methyltransferase 8 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20161124 MGI PMID:26665171 1558440 Prmt8 protein arginine N-methyltransferase 8 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20161124 MGI PMID:26665171 1558440 Prmt8 protein arginine N-methyltransferase 8 gene MP:0001513 limb grasping IAGP N RGD:5509061 20161124 MGI PMID:26665171 1558440 Prmt8 protein arginine N-methyltransferase 8 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20161124 MGI PMID:26665171 1558440 Prmt8 protein arginine N-methyltransferase 8 gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20161124 MGI PMID:26665171 1558440 Prmt8 protein arginine N-methyltransferase 8 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20161124 MGI PMID:26665171 1558441 C1d C1D nuclear receptor co-repressor gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20230119 MGI 1558441 C1d C1D nuclear receptor co-repressor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1558442 Pgk2 phosphoglycerate kinase 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:19759366 1558442 Pgk2 phosphoglycerate kinase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19759366 1558442 Pgk2 phosphoglycerate kinase 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19759366 1558442 Pgk2 phosphoglycerate kinase 2 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220303 MGI PMID:19759366 1558445 Mid2 midline 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 1558445 Mid2 midline 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20181227 MGI 1558445 Mid2 midline 2 gene MP:0001192 scaly skin IEA N RGD:5509061 20181227 MGI 1558445 Mid2 midline 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1558448 Kdm4b lysine (K)-specific demethylase 4B gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:21445275 1558448 Kdm4b lysine (K)-specific demethylase 4B gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:21445275 1558448 Kdm4b lysine (K)-specific demethylase 4B gene MP:0000771 abnormal brain size IAGP N RGD:5509061 20210311 MGI PMID:33232677 1558448 Kdm4b lysine (K)-specific demethylase 4B gene MP:0001257 increased body length IEA N RGD:5509061 20160804 MGI 1558448 Kdm4b lysine (K)-specific demethylase 4B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21445275 1558448 Kdm4b lysine (K)-specific demethylase 4B gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20210311 MGI PMID:33232677 1558448 Kdm4b lysine (K)-specific demethylase 4B gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1558448 Kdm4b lysine (K)-specific demethylase 4B gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20160804 MGI 1558448 Kdm4b lysine (K)-specific demethylase 4B gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160804 MGI 1558448 Kdm4b lysine (K)-specific demethylase 4B gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20210311 MGI PMID:33232677 1558448 Kdm4b lysine (K)-specific demethylase 4B gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21445275 1558448 Kdm4b lysine (K)-specific demethylase 4B gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20210311 MGI PMID:33232677 1558448 Kdm4b lysine (K)-specific demethylase 4B gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210311 MGI PMID:33232677 1558448 Kdm4b lysine (K)-specific demethylase 4B gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20210311 MGI PMID:33232677 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000111 cleft palate IAGP N RGD:5509061 20220915 MGI PMID:32541010 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:22826230 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:22949634 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000913 abnormal brain development IEA N RGD:5509061 20111116 MGI 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22949634 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000919 cranioschisis IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:22801502 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:22949634 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22949634 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0001577 anemia IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22826230 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22949634 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0002083 premature death IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:22826230 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22826230 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:22949634 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:22949634 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20111116 MGI 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0003400 kinked neural tube IEA N RGD:5509061 20111116 MGI 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:22826230 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:22949634 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0003794 delayed somite formation IAGP N RGD:5509061 20141003 MGI PMID:22826230 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22801502 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:22949634 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:22826230 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:22949634 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:22801502 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:22826230 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:22826230 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22949634 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22949634 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23028370 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23365460 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22801502 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22826230 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0012185 abnormal muscle precursor cell morphology IAGP N RGD:5509061 20160721 MGI PMID:26999603 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0012754 abnormal cranial neural crest cell morphology IAGP N RGD:5509061 20220915 MGI PMID:32541010 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20160721 MGI PMID:26999603 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0013545 cleft hard palate IAGP N RGD:5509061 20220915 MGI PMID:32541010 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0013696 increased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558450 Kdm6a lysine (K)-specific demethylase 6A gene MP:0013705 decreased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20180830 MGI PMID:29479066 1558451 Kcnk7 potassium channel, subfamily K, member 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18572259 1558452 Slc25a23 solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:23344948 1558452 Slc25a23 solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23 gene MP:0011467 decreased urine urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23344948 1558453 Sh2d1b1 SH2 domain containing 1B1 gene MP:0003080 increased natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:16127454 1558453 Sh2d1b1 SH2 domain containing 1B1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:19151721 1558453 Sh2d1b1 SH2 domain containing 1B1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:20962259 1558453 Sh2d1b1 SH2 domain containing 1B1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16127454 1558453 Sh2d1b1 SH2 domain containing 1B1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20962259 1558453 Sh2d1b1 SH2 domain containing 1B1 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22683124 1558454 Itga4 integrin alpha 4 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14645544 1558454 Itga4 integrin alpha 4 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16470243 1558454 Itga4 integrin alpha 4 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:7539359 1558454 Itga4 integrin alpha 4 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:7539359 1558454 Itga4 integrin alpha 4 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:7539359 1558454 Itga4 integrin alpha 4 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14645544 1558454 Itga4 integrin alpha 4 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:7539359 1558454 Itga4 integrin alpha 4 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14645544 1558454 Itga4 integrin alpha 4 gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:14645544 1558454 Itga4 integrin alpha 4 gene MP:0002424 abnormal reticulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14645544 1558454 Itga4 integrin alpha 4 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16470243 1558454 Itga4 integrin alpha 4 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16470243 1558454 Itga4 integrin alpha 4 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:18809756 1558454 Itga4 integrin alpha 4 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:18809756 1558454 Itga4 integrin alpha 4 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:16470243 1558454 Itga4 integrin alpha 4 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16470243 1558454 Itga4 integrin alpha 4 gene MP:0004557 dilated allantois IAGP N RGD:5509061 20141003 MGI PMID:7539359 1558454 Itga4 integrin alpha 4 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18809756 1558454 Itga4 integrin alpha 4 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18809756 1558454 Itga4 integrin alpha 4 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18809756 1558454 Itga4 integrin alpha 4 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18583710 1558454 Itga4 integrin alpha 4 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14645544 1558454 Itga4 integrin alpha 4 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:16470243 1558454 Itga4 integrin alpha 4 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:18809756 1558454 Itga4 integrin alpha 4 gene MP:0008247 abnormal mononuclear cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18809756 1558454 Itga4 integrin alpha 4 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12021259 1558454 Itga4 integrin alpha 4 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:7539359 1558454 Itga4 integrin alpha 4 gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12021259 1558454 Itga4 integrin alpha 4 gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7539359 1558454 Itga4 integrin alpha 4 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:18809756 1558454 Itga4 integrin alpha 4 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:7539359 1558454 Itga4 integrin alpha 4 gene MP:0010555 absent epicardium IAGP N RGD:5509061 20240229 MGI PMID:12021259 1558454 Itga4 integrin alpha 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12021259 1558454 Itga4 integrin alpha 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7539359 1558454 Itga4 integrin alpha 4 gene MP:0031590 abnormal epicardium development IAGP N RGD:5509061 20240229 MGI PMID:12021259 1558454 Itga4 integrin alpha 4 gene MP:0031590 abnormal epicardium development IAGP N RGD:5509061 20240229 MGI PMID:7539359 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0002183 gliosis IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558456 Acot7 acyl-CoA thioesterase 7 gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20200310 MGI PMID:23459938 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:19637241 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14961764 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:19637241 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:19637241 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0002717 abnormal male preputial gland morphology IAGP N RGD:5509061 20141003 MGI PMID:14961764 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0002717 abnormal male preputial gland morphology IAGP N RGD:5509061 20141003 MGI PMID:19637241 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19637241 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:19637241 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19637241 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:19637241 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:19637241 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19637241 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19637241 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19637241 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:19637241 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19637241 1558458 Uaca uveal autoantigen with coiled-coil domains and ankyrin repeats gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210218 MGI PMID:19637241 1558459 Ubn2 ubinuclein 2 gene MP:0000914 exencephaly IEA N RGD:5509061 20221215 MGI 1558459 Ubn2 ubinuclein 2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210826 MGI 1558459 Ubn2 ubinuclein 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1558459 Ubn2 ubinuclein 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210826 MGI 1558459 Ubn2 ubinuclein 2 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1558459 Ubn2 ubinuclein 2 gene MP:0003717 pallor IEA N RGD:5509061 20230601 MGI 1558459 Ubn2 ubinuclein 2 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20210826 MGI 1558459 Ubn2 ubinuclein 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1558459 Ubn2 ubinuclein 2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1558459 Ubn2 ubinuclein 2 gene MP:0009263 abnormal eyelid fusion IEA N RGD:5509061 20221215 MGI 1558459 Ubn2 ubinuclein 2 gene MP:0009908 protruding tongue IEA N RGD:5509061 20221215 MGI 1558459 Ubn2 ubinuclein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1558459 Ubn2 ubinuclein 2 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20210826 MGI 1558459 Ubn2 ubinuclein 2 gene MP:0011496 abnormal head size IEA N RGD:5509061 20210826 MGI 1558462 Lax1 lymphocyte transmembrane adaptor 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:15843560 1558462 Lax1 lymphocyte transmembrane adaptor 1 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:15843560 1558462 Lax1 lymphocyte transmembrane adaptor 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15843560 1558462 Lax1 lymphocyte transmembrane adaptor 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15843560 1558462 Lax1 lymphocyte transmembrane adaptor 1 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:15843560 1558462 Lax1 lymphocyte transmembrane adaptor 1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15843560 1558462 Lax1 lymphocyte transmembrane adaptor 1 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:15843560 1558462 Lax1 lymphocyte transmembrane adaptor 1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:15843560 1558462 Lax1 lymphocyte transmembrane adaptor 1 gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:15843560 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000019 thick ears IAGP N RGD:5509061 20141003 MGI PMID:16397132 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20181227 MGI 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16122996 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20141003 MGI PMID:16397132 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:16122996 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:1686018 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000573 increased hindlimb autopod size IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000580 deformed nails IAGP N RGD:5509061 20141003 MGI PMID:16122996 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:16122996 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:1686018 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20181227 MGI 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16122996 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:16397132 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:16397132 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:16397132 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:16397132 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0001849 ear inflammation IAGP N RGD:5509061 20141003 MGI PMID:16122996 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0001849 ear inflammation IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:16397132 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20181227 MGI 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20181227 MGI 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:16122996 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:16122996 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16397132 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16397132 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:1686018 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20221215 MGI 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16397132 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:16397132 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:16397132 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0005190 osteomyelitis IAGP N RGD:5509061 20141003 MGI PMID:10678414 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0005190 osteomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16122996 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:16397132 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22646813 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16397132 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16397132 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1558463 Pstpip2 proline-serine-threonine phosphatase-interacting protein 2 gene MP:0030422 abnormal outer ear cartilage morphology IAGP N RGD:5509061 20171214 MGI PMID:16122996 1558464 Tspan33 tetraspanin 33 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:17158226 1558464 Tspan33 tetraspanin 33 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17158226 1558464 Tspan33 tetraspanin 33 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17158226 1558464 Tspan33 tetraspanin 33 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:17158226 1558464 Tspan33 tetraspanin 33 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17158226 1558464 Tspan33 tetraspanin 33 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17158226 1558464 Tspan33 tetraspanin 33 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17158226 1558464 Tspan33 tetraspanin 33 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17158226 1558464 Tspan33 tetraspanin 33 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:17158226 1558464 Tspan33 tetraspanin 33 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17158226 1558464 Tspan33 tetraspanin 33 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17158226 1558464 Tspan33 tetraspanin 33 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17158226 1558464 Tspan33 tetraspanin 33 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:17158226 1558464 Tspan33 tetraspanin 33 gene MP:0010175 leptocytosis IAGP N RGD:5509061 20141003 MGI PMID:17158226 1558466 Lrrc51 leucine rich repeat containing 51 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1558466 Lrrc51 leucine rich repeat containing 51 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20190502 MGI 1558466 Lrrc51 leucine rich repeat containing 51 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1558467 Shb src homology 2 domain-containing transforming protein B gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17676633 1558467 Shb src homology 2 domain-containing transforming protein B gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17676633 1558467 Shb src homology 2 domain-containing transforming protein B gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17676633 1558467 Shb src homology 2 domain-containing transforming protein B gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:17676633 1558467 Shb src homology 2 domain-containing transforming protein B gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20141003 MGI PMID:17676633 1558467 Shb src homology 2 domain-containing transforming protein B gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17676633 1558467 Shb src homology 2 domain-containing transforming protein B gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17676633 1558468 Marco macrophage receptor with collagenous structure gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1558468 Marco macrophage receptor with collagenous structure gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 1558468 Marco macrophage receptor with collagenous structure gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:15263032 1558468 Marco macrophage receptor with collagenous structure gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15263032 1558468 Marco macrophage receptor with collagenous structure gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16339556 1558468 Marco macrophage receptor with collagenous structure gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23840879 1558468 Marco macrophage receptor with collagenous structure gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15263032 1558468 Marco macrophage receptor with collagenous structure gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16339556 1558468 Marco macrophage receptor with collagenous structure gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15263032 1558468 Marco macrophage receptor with collagenous structure gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16339556 1558468 Marco macrophage receptor with collagenous structure gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16339556 1558468 Marco macrophage receptor with collagenous structure gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 1558468 Marco macrophage receptor with collagenous structure gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23840879 1558468 Marco macrophage receptor with collagenous structure gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15263032 1558468 Marco macrophage receptor with collagenous structure gene MP:0010740 abnormal dendritic cell chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:23840879 1558470 Osbpl10 oxysterol binding protein-like 10 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1558471 Tceal9 transcription elongation factor A like 9 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1558471 Tceal9 transcription elongation factor A like 9 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1558472 Aimp2 aminoacyl tRNA synthetase complex-interacting multifunctional protein 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12060739 1558473 Ddx54 DEAD box helicase 54 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1558473 Ddx54 DEAD box helicase 54 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558473 Ddx54 DEAD box helicase 54 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1558473 Ddx54 DEAD box helicase 54 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1558474 Dip2a disco interacting protein 2 homolog A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210603 MGI PMID:33184751 1558474 Dip2a disco interacting protein 2 homolog A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210603 MGI PMID:33184751 1558474 Dip2a disco interacting protein 2 homolog A gene MP:0003053 delayed tooth eruption IAGP N RGD:5509061 20210603 MGI PMID:33184751 1558474 Dip2a disco interacting protein 2 homolog A gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20210603 MGI PMID:33184751 1558474 Dip2a disco interacting protein 2 homolog A gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20211021 MGI 1558475 Gen1 GEN1, Holliday junction 5' flap endonuclease gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20190530 MGI PMID:29483821 1558475 Gen1 GEN1, Holliday junction 5' flap endonuclease gene MP:0000585 kinked tail IAGP N RGD:5509061 20190530 MGI PMID:29483821 1558475 Gen1 GEN1, Holliday junction 5' flap endonuclease gene MP:0001948 vesicoureteral reflux IAGP N RGD:5509061 20190530 MGI PMID:29483821 1558475 Gen1 GEN1, Holliday junction 5' flap endonuclease gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20190530 MGI PMID:29483821 1558475 Gen1 GEN1, Holliday junction 5' flap endonuclease gene MP:0003604 single kidney IAGP N RGD:5509061 20190530 MGI PMID:29483821 1558475 Gen1 GEN1, Holliday junction 5' flap endonuclease gene MP:0004017 duplex kidney IAGP N RGD:5509061 20190530 MGI PMID:29483821 1558475 Gen1 GEN1, Holliday junction 5' flap endonuclease gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20190530 MGI PMID:29483821 1558475 Gen1 GEN1, Holliday junction 5' flap endonuclease gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20230126 MGI PMID:27383418 1558475 Gen1 GEN1, Holliday junction 5' flap endonuclease gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20190530 MGI PMID:29483821 1558475 Gen1 GEN1, Holliday junction 5' flap endonuclease gene MP:0010980 ectopic ureteric bud IAGP N RGD:5509061 20190530 MGI PMID:29483821 1558475 Gen1 GEN1, Holliday junction 5' flap endonuclease gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230126 MGI PMID:27383418 1558475 Gen1 GEN1, Holliday junction 5' flap endonuclease gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20230126 MGI PMID:27383418 1558475 Gen1 GEN1, Holliday junction 5' flap endonuclease gene MP:0014040 increased cellular sensitivity to DNA damaging agents IAGP N RGD:5509061 20230126 MGI PMID:27383418 1558476 Endov endonuclease V gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20240523 MGI 1558476 Endov endonuclease V gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1558476 Endov endonuclease V gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20200910 MGI PMID:32083667 1558476 Endov endonuclease V gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20240523 MGI 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23376831 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20151217 MGI PMID:26311765 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20151217 MGI PMID:26311765 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18542050 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170323 MGI 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21709234 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18542050 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:23596170 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18542050 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:23596170 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0003332 liver abscess IAGP N RGD:5509061 20141003 MGI PMID:21709234 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23376831 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:23376831 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:23376831 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20151217 MGI PMID:26311765 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:23376831 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:21709234 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:21709234 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0008618 decreased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:21709234 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0008648 decreased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:21709234 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:21709234 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18542050 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:18542050 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:18542050 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20151217 MGI PMID:26311765 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21709234 1558477 Trpm2 transient receptor potential cation channel, subfamily M, member 2 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:23376831 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20231207 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20220519 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20220811 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0000650 mesocardia IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20231207 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:12560552 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20231207 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:12560552 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12560552 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20231207 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17083490 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20220811 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:12560552 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:12560552 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20220811 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20221215 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20220519 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220519 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:12560552 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:12560552 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20240523 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0010334 pleural effusion IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20210128 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0010426 abnormal heart and great artery attachment IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0010436 abnormal coronary sinus morphology IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0010488 abnormal left subclavian artery morphology IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0010854 lung situs inversus IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17075880 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20200402 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20220811 MGI 1558478 Mgrn1 mahogunin, ring finger 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20231207 MGI 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:18689798 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:18689798 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20141003 MGI PMID:18689798 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:18689798 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:18689798 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:18689798 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:15694322 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:18689798 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:15694322 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0006363 absent auchene hairs IAGP N RGD:5509061 20141003 MGI PMID:18689798 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0006365 absent guard hair IAGP N RGD:5509061 20141003 MGI PMID:18689798 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0006366 absent zigzag hairs IAGP N RGD:5509061 20141003 MGI PMID:18689798 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0006367 absent sweat gland IAGP N RGD:5509061 20141003 MGI PMID:18689798 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0006400 decreased molar number IAGP N RGD:5509061 20141003 MGI PMID:18689798 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0013370 anhidrosis IAGP N RGD:5509061 20141225 MGI PMID:18689798 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20180125 MGI PMID:18689798 1558479 Tnfrsf19 tumor necrosis factor receptor superfamily, member 19 gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:22340501 1558480 H3c14 H3 clustered histone 14 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20190815 MGI PMID:30991053 1558480 H3c14 H3 clustered histone 14 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20190815 MGI PMID:30991053 1558480 H3c14 H3 clustered histone 14 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20190815 MGI PMID:30991053 1558480 H3c14 H3 clustered histone 14 gene MP:0001329 retina hyperplasia IAGP N RGD:5509061 20190815 MGI PMID:30991053 1558480 H3c14 H3 clustered histone 14 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20190815 MGI PMID:30991053 1558480 H3c14 H3 clustered histone 14 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20190815 MGI PMID:30991053 1558480 H3c14 H3 clustered histone 14 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20190815 MGI PMID:30991053 1558480 H3c14 H3 clustered histone 14 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20190815 MGI PMID:30991053 1558480 H3c14 H3 clustered histone 14 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20190815 MGI PMID:30991053 1558480 H3c14 H3 clustered histone 14 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20190815 MGI PMID:30991053 1558480 H3c14 H3 clustered histone 14 gene MP:0031206 hypolipidemia IAGP N RGD:5509061 20210211 MGI PMID:30991053 1558480 H3c14 H3 clustered histone 14 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:30991053 1558481 Tsku tsukushi, small leucine rich proteoglycan gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:21055390 1558481 Tsku tsukushi, small leucine rich proteoglycan gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:21055390 1558481 Tsku tsukushi, small leucine rich proteoglycan gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:21055390 1558482 Ranbp2 RAN binding protein 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1558482 Ranbp2 RAN binding protein 2 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1558482 Ranbp2 RAN binding protein 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18394993 1558482 Ranbp2 RAN binding protein 2 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18394993 1558482 Ranbp2 RAN binding protein 2 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1558482 Ranbp2 RAN binding protein 2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18394993 1558482 Ranbp2 RAN binding protein 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:17069463 1558482 Ranbp2 RAN binding protein 2 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241010 MGI 1558482 Ranbp2 RAN binding protein 2 gene MP:0003701 elevated level of mitotic sister chromatid exchange IAGP N RGD:5509061 20141003 MGI PMID:18394993 1558482 Ranbp2 RAN binding protein 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17069463 1558482 Ranbp2 RAN binding protein 2 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:18394993 1558482 Ranbp2 RAN binding protein 2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:18394993 1558482 Ranbp2 RAN binding protein 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:18394993 1558482 Ranbp2 RAN binding protein 2 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 1558482 Ranbp2 RAN binding protein 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17069463 1558482 Ranbp2 RAN binding protein 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17069463 1558482 Ranbp2 RAN binding protein 2 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18394993 1558482 Ranbp2 RAN binding protein 2 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:18394993 1558482 Ranbp2 RAN binding protein 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17069463 1558482 Ranbp2 RAN binding protein 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18394993 1558482 Ranbp2 RAN binding protein 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241010 MGI 1558482 Ranbp2 RAN binding protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558482 Ranbp2 RAN binding protein 2 gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20241010 MGI 1558482 Ranbp2 RAN binding protein 2 gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20241010 MGI 1558482 Ranbp2 RAN binding protein 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1558482 Ranbp2 RAN binding protein 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1558483 Patj PATJ, crumbs cell polarity complex component gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1558483 Patj PATJ, crumbs cell polarity complex component gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1558483 Patj PATJ, crumbs cell polarity complex component gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 1558484 Slamf7 SLAM family member 7 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:19151721 1558487 Pabpc5 poly(A) binding protein, cytoplasmic 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1558487 Pabpc5 poly(A) binding protein, cytoplasmic 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1558487 Pabpc5 poly(A) binding protein, cytoplasmic 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1558487 Pabpc5 poly(A) binding protein, cytoplasmic 5 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1558491 Zfp329 zinc finger protein 329 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1558491 Zfp329 zinc finger protein 329 gene MP:0002546 mydriasis IEA N RGD:5509061 20240523 MGI 1558491 Zfp329 zinc finger protein 329 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20201231 MGI 1558491 Zfp329 zinc finger protein 329 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1558492 Bex2 brain expressed X-linked 2 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1558492 Bex2 brain expressed X-linked 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1558492 Bex2 brain expressed X-linked 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1558492 Bex2 brain expressed X-linked 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1558492 Bex2 brain expressed X-linked 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1558492 Bex2 brain expressed X-linked 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160421 MGI 1558492 Bex2 brain expressed X-linked 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201224 MGI PMID:25143383 1558492 Bex2 brain expressed X-linked 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1558492 Bex2 brain expressed X-linked 2 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1558493 Slitrk3 SLIT and NTRK-like family, member 3 gene MP:0002064 seizures IAGP N RGD:5509061 20160804 MGI PMID:22286174 1558493 Slitrk3 SLIT and NTRK-like family, member 3 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20160804 MGI PMID:22286174 1558493 Slitrk3 SLIT and NTRK-like family, member 3 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20160804 MGI PMID:22286174 1558493 Slitrk3 SLIT and NTRK-like family, member 3 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:22286174 1558494 Usp4 ubiquitin specific peptidase 4 (proto-oncogene) gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:21522127 1558494 Usp4 ubiquitin specific peptidase 4 (proto-oncogene) gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20240516 MGI PMID:30514904 1558494 Usp4 ubiquitin specific peptidase 4 (proto-oncogene) gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21522127 1558494 Usp4 ubiquitin specific peptidase 4 (proto-oncogene) gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21522127 1558494 Usp4 ubiquitin specific peptidase 4 (proto-oncogene) gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:21522127 1558494 Usp4 ubiquitin specific peptidase 4 (proto-oncogene) gene MP:0009322 increased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21522127 1558494 Usp4 ubiquitin specific peptidase 4 (proto-oncogene) gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21522127 1558497 Tlr7 toll-like receptor 7 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18606711 1558497 Tlr7 toll-like receptor 7 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17997333 1558497 Tlr7 toll-like receptor 7 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0000701 abnormal lymph node size IAGP N RGD:5509061 20141003 MGI PMID:16973389 1558497 Tlr7 toll-like receptor 7 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1558497 Tlr7 toll-like receptor 7 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1558497 Tlr7 toll-like receptor 7 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:17997333 1558497 Tlr7 toll-like receptor 7 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17997333 1558497 Tlr7 toll-like receptor 7 gene MP:0002083 premature death IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17997333 1558497 Tlr7 toll-like receptor 7 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20811154 1558497 Tlr7 toll-like receptor 7 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16461338 1558497 Tlr7 toll-like receptor 7 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16973389 1558497 Tlr7 toll-like receptor 7 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1558497 Tlr7 toll-like receptor 7 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1558497 Tlr7 toll-like receptor 7 gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:18606711 1558497 Tlr7 toll-like receptor 7 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:18606711 1558497 Tlr7 toll-like receptor 7 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0002870 decreased anti-insulin autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1558497 Tlr7 toll-like receptor 7 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1558497 Tlr7 toll-like receptor 7 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1558497 Tlr7 toll-like receptor 7 gene MP:0003865 lymph node inflammation IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:17997333 1558497 Tlr7 toll-like receptor 7 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:17997333 1558497 Tlr7 toll-like receptor 7 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:16973389 1558497 Tlr7 toll-like receptor 7 gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1558497 Tlr7 toll-like receptor 7 gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:18606711 1558497 Tlr7 toll-like receptor 7 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16973389 1558497 Tlr7 toll-like receptor 7 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16973389 1558497 Tlr7 toll-like receptor 7 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:20811154 1558497 Tlr7 toll-like receptor 7 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17997333 1558497 Tlr7 toll-like receptor 7 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:20811154 1558497 Tlr7 toll-like receptor 7 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:20811154 1558497 Tlr7 toll-like receptor 7 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:16973389 1558497 Tlr7 toll-like receptor 7 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1558497 Tlr7 toll-like receptor 7 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1558497 Tlr7 toll-like receptor 7 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1558497 Tlr7 toll-like receptor 7 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:16973389 1558497 Tlr7 toll-like receptor 7 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0008561 decreased tumor necrosis factor secretion IEA N RGD:5509061 20111116 MGI 1558497 Tlr7 toll-like receptor 7 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20200423 MGI PMID:16985170 1558497 Tlr7 toll-like receptor 7 gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:15034168 1558497 Tlr7 toll-like receptor 7 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:16461338 1558497 Tlr7 toll-like receptor 7 gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16973389 1558497 Tlr7 toll-like receptor 7 gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0009318 increased splenic marginal zone lymphoma incidence IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17997333 1558497 Tlr7 toll-like receptor 7 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17997333 1558497 Tlr7 toll-like receptor 7 gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558497 Tlr7 toll-like receptor 7 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20220623 MGI PMID:35477763 1558498 Mbtps2 membrane-bound transcription factor peptidase, site 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20240404 MGI PMID:37797712 1558498 Mbtps2 membrane-bound transcription factor peptidase, site 2 gene MP:0006205 embryonic lethality between implantation and somite formation IAGP N RGD:5509061 20240404 MGI PMID:37797712 1558498 Mbtps2 membrane-bound transcription factor peptidase, site 2 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20240404 MGI PMID:37797712 1558498 Mbtps2 membrane-bound transcription factor peptidase, site 2 gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20240404 MGI PMID:37797712 1558498 Mbtps2 membrane-bound transcription factor peptidase, site 2 gene MP:0011692 increased chondrocyte number IAGP N RGD:5509061 20240404 MGI PMID:37797712 1558498 Mbtps2 membrane-bound transcription factor peptidase, site 2 gene MP:0014025 decreased subchondral bone mineral content IAGP N RGD:5509061 20240404 MGI PMID:37797712 1558498 Mbtps2 membrane-bound transcription factor peptidase, site 2 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20240404 MGI PMID:37797712 1558498 Mbtps2 membrane-bound transcription factor peptidase, site 2 gene MP:0030486 abnormal osteocyte canaliculus morphology IAGP N RGD:5509061 20240404 MGI PMID:37797712 1558500 Dusp3 dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related) gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1558500 Dusp3 dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related) gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20160929 MGI PMID:24886454 1558500 Dusp3 dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related) gene MP:0003443 increased circulating glycerol level IEA N RGD:5509061 20200514 MGI 1558500 Dusp3 dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related) gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20141003 MGI 1558500 Dusp3 dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related) gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20141003 MGI 1558500 Dusp3 dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related) gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20160804 MGI 1558500 Dusp3 dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related) gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20160929 MGI PMID:24886454 1558500 Dusp3 dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related) gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1558500 Dusp3 dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related) gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20200514 MGI 1558500 Dusp3 dual specificity phosphatase 3 (vaccinia virus phosphatase VH1-related) gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20201022 MGI 1558502 Atg7 autophagy related 7 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:21339326 1558502 Atg7 autophagy related 7 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1558502 Atg7 autophagy related 7 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1558502 Atg7 autophagy related 7 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20200310 MGI PMID:21339326 1558502 Atg7 autophagy related 7 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:15866887 1558502 Atg7 autophagy related 7 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20200310 MGI PMID:15866887 1558502 Atg7 autophagy related 7 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:15866887 1558502 Atg7 autophagy related 7 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20200310 MGI PMID:15866887 1558502 Atg7 autophagy related 7 gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20210128 MGI 1558502 Atg7 autophagy related 7 gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:20439739 1558502 Atg7 autophagy related 7 gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:23152632 1558502 Atg7 autophagy related 7 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:23152632 1558502 Atg7 autophagy related 7 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20201231 MGI PMID:33082312 1558502 Atg7 autophagy related 7 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:23095749 1558502 Atg7 autophagy related 7 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:20439739 1558502 Atg7 autophagy related 7 gene MP:0001147 small testis IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:15866887 1558502 Atg7 autophagy related 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:23152632 1558502 Atg7 autophagy related 7 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1558502 Atg7 autophagy related 7 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20200310 MGI PMID:25155956 1558502 Atg7 autophagy related 7 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20200310 MGI PMID:23152632 1558502 Atg7 autophagy related 7 gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:23152632 1558502 Atg7 autophagy related 7 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:23152632 1558502 Atg7 autophagy related 7 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1558502 Atg7 autophagy related 7 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20201231 MGI PMID:33082312 1558502 Atg7 autophagy related 7 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:23152632 1558502 Atg7 autophagy related 7 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:20439739 1558502 Atg7 autophagy related 7 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20200310 MGI PMID:15866887 1558502 Atg7 autophagy related 7 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210128 MGI 1558502 Atg7 autophagy related 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20201231 MGI PMID:33082312 1558502 Atg7 autophagy related 7 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20200310 MGI PMID:26214133 1558502 Atg7 autophagy related 7 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20200310 MGI PMID:24089213 1558502 Atg7 autophagy related 7 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1558502 Atg7 autophagy related 7 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20200310 MGI PMID:25290687 1558502 Atg7 autophagy related 7 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:23152632 1558502 Atg7 autophagy related 7 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:29438013 1558502 Atg7 autophagy related 7 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:23152632 1558502 Atg7 autophagy related 7 gene MP:0002183 gliosis IAGP N RGD:5509061 20200310 MGI PMID:20439739 1558502 Atg7 autophagy related 7 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200310 MGI PMID:20439739 1558502 Atg7 autophagy related 7 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:23152632 1558502 Atg7 autophagy related 7 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:15866887 1558502 Atg7 autophagy related 7 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20210826 MGI 1558502 Atg7 autophagy related 7 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20200310 MGI PMID:15866887 1558502 Atg7 autophagy related 7 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:15866887 1558502 Atg7 autophagy related 7 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0003051 curly tail IAGP N RGD:5509061 20200310 MGI PMID:20439739 1558502 Atg7 autophagy related 7 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:20439739 1558502 Atg7 autophagy related 7 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:23152632 1558502 Atg7 autophagy related 7 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20200310 MGI PMID:24089213 1558502 Atg7 autophagy related 7 gene MP:0003325 decreased liver function IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200310 MGI PMID:23152632 1558502 Atg7 autophagy related 7 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20200310 MGI PMID:24185898 1558502 Atg7 autophagy related 7 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20200310 MGI PMID:26214133 1558502 Atg7 autophagy related 7 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:25290687 1558502 Atg7 autophagy related 7 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20201231 MGI PMID:33082312 1558502 Atg7 autophagy related 7 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20200310 MGI PMID:21339326 1558502 Atg7 autophagy related 7 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20200310 MGI PMID:21339326 1558502 Atg7 autophagy related 7 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20200310 MGI PMID:26214133 1558502 Atg7 autophagy related 7 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20200310 MGI PMID:26214133 1558502 Atg7 autophagy related 7 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:21339326 1558502 Atg7 autophagy related 7 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:21339326 1558502 Atg7 autophagy related 7 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20200310 MGI PMID:25290687 1558502 Atg7 autophagy related 7 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:29438013 1558502 Atg7 autophagy related 7 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20200310 MGI PMID:20439739 1558502 Atg7 autophagy related 7 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20200310 MGI PMID:15866887 1558502 Atg7 autophagy related 7 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20200310 MGI PMID:15866887 1558502 Atg7 autophagy related 7 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200310 MGI PMID:15866887 1558502 Atg7 autophagy related 7 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20201231 MGI PMID:33082312 1558502 Atg7 autophagy related 7 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 1558502 Atg7 autophagy related 7 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20200310 MGI PMID:23152632 1558502 Atg7 autophagy related 7 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20200310 MGI PMID:25290687 1558502 Atg7 autophagy related 7 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20200310 MGI PMID:21339326 1558502 Atg7 autophagy related 7 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:26214133 1558502 Atg7 autophagy related 7 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:21339326 1558502 Atg7 autophagy related 7 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20200310 MGI PMID:21339326 1558502 Atg7 autophagy related 7 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20200310 MGI PMID:24089213 1558502 Atg7 autophagy related 7 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20200310 MGI PMID:25155956 1558502 Atg7 autophagy related 7 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20200310 MGI PMID:25290687 1558502 Atg7 autophagy related 7 gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:26214133 1558502 Atg7 autophagy related 7 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20200310 MGI PMID:26214133 1558502 Atg7 autophagy related 7 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:23152632 1558502 Atg7 autophagy related 7 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20200310 MGI PMID:21339326 1558502 Atg7 autophagy related 7 gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:24089213 1558502 Atg7 autophagy related 7 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20201231 MGI PMID:33082312 1558502 Atg7 autophagy related 7 gene MP:0009387 abnormal epidermal pigmentation IAGP N RGD:5509061 20200310 MGI PMID:25290687 1558502 Atg7 autophagy related 7 gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:25290687 1558502 Atg7 autophagy related 7 gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20200310 MGI PMID:24089213 1558502 Atg7 autophagy related 7 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20200310 MGI PMID:25155956 1558502 Atg7 autophagy related 7 gene MP:0009972 absent hippocampus pyramidal cells IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0009975 absent cerebral cortex pyramidal cells IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20200310 MGI PMID:26214133 1558502 Atg7 autophagy related 7 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20200310 MGI PMID:27096368 1558502 Atg7 autophagy related 7 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20200310 MGI PMID:26214133 1558502 Atg7 autophagy related 7 gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20200310 MGI PMID:29438013 1558502 Atg7 autophagy related 7 gene MP:0010741 abnormal melanocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:25290687 1558502 Atg7 autophagy related 7 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20200310 MGI PMID:21339326 1558502 Atg7 autophagy related 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29438013 1558502 Atg7 autophagy related 7 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15866887 1558502 Atg7 autophagy related 7 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20201231 MGI PMID:33082312 1558502 Atg7 autophagy related 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1558502 Atg7 autophagy related 7 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20201231 MGI PMID:33082312 1558502 Atg7 autophagy related 7 gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20200310 MGI PMID:25290687 1558502 Atg7 autophagy related 7 gene MP:0011568 decreased foot pigmentation IAGP N RGD:5509061 20200310 MGI PMID:25290687 1558502 Atg7 autophagy related 7 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20200310 MGI PMID:25290687 1558502 Atg7 autophagy related 7 gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20201231 MGI PMID:33082312 1558502 Atg7 autophagy related 7 gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:26214133 1558502 Atg7 autophagy related 7 gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20200310 MGI PMID:23152632 1558502 Atg7 autophagy related 7 gene MP:0013654 increased CD103-positive CD11b-low dendritic cell number IAGP N RGD:5509061 20200310 MGI PMID:26214133 1558502 Atg7 autophagy related 7 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20201231 MGI PMID:33082312 1558502 Atg7 autophagy related 7 gene MP:0014239 abnormal intracellular organelle morphology IAGP N RGD:5509061 20230615 MGI PMID:15866887 1558502 Atg7 autophagy related 7 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:15866887 1558502 Atg7 autophagy related 7 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20200310 MGI PMID:25155956 1558502 Atg7 autophagy related 7 gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20200310 MGI PMID:29438013 1558502 Atg7 autophagy related 7 gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200310 MGI PMID:18083104 1558502 Atg7 autophagy related 7 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200310 MGI PMID:25155956 1558502 Atg7 autophagy related 7 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558502 Atg7 autophagy related 7 gene MP:0031355 abnormal proacrosomal vesicle fusion IAGP N RGD:5509061 20220303 MGI PMID:24853953 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23576758 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20231109 MGI PMID:23637775 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20240104 MGI PMID:23637775 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0000601 small liver IEA N RGD:5509061 20170105 MGI 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0000692 small spleen IEA N RGD:5509061 20170105 MGI 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23576758 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0001657 abnormal induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20141003 MGI PMID:19098913 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:21357675 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:19098913 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:19098913 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:19098913 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0002188 small heart IEA N RGD:5509061 20170105 MGI 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210520 MGI 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23576758 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23576758 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20170504 MGI PMID:24735673 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0002989 small kidney IEA N RGD:5509061 20170105 MGI 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:17392792 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0003216 absence seizures IAGP N RGD:5509061 20170504 MGI PMID:24735673 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0003641 small lung IEA N RGD:5509061 20170105 MGI 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141003 MGI PMID:17392792 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0003965 abnormal pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:17392792 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0003969 abnormal luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:17392792 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20170504 MGI PMID:24735673 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20170504 MGI PMID:24735673 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17392792 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:17392792 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19098913 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0009416 cardiac muscle degeneration IAGP N RGD:5509061 20231109 MGI PMID:23637775 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20170504 MGI PMID:24735673 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160421 MGI 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:23637775 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20240125 MGI PMID:23637775 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:23637775 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21357675 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17392792 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19098913 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21357675 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21357675 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21357675 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:23637775 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0011243 decreased fetal derived definitive erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23795291 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0020471 abnormal circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:24582500 1558503 Kdm1a lysine (K)-specific demethylase 1A gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:24582500 1558504 Cep43 centrosomal protein 43 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201022 MGI 1558504 Cep43 centrosomal protein 43 gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1558504 Cep43 centrosomal protein 43 gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20211021 MGI 1558504 Cep43 centrosomal protein 43 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1558504 Cep43 centrosomal protein 43 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 1558504 Cep43 centrosomal protein 43 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1558504 Cep43 centrosomal protein 43 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1558504 Cep43 centrosomal protein 43 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558505 Usp50 ubiquitin specific peptidase 50 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20170105 MGI 1558505 Usp50 ubiquitin specific peptidase 50 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1558505 Usp50 ubiquitin specific peptidase 50 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558506 Fahd2a fumarylacetoacetate hydrolase domain containing 2A gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20160804 MGI 1558506 Fahd2a fumarylacetoacetate hydrolase domain containing 2A gene MP:0001257 increased body length IEA N RGD:5509061 20160804 MGI 1558506 Fahd2a fumarylacetoacetate hydrolase domain containing 2A gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160804 MGI 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20180215 MGI PMID:27562646 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180215 MGI PMID:27562646 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:23035106 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0002802 abnormal discrimination learning IAGP N RGD:5509061 20141003 MGI PMID:23035106 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:23035106 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:23035106 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20180215 MGI PMID:27562646 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20170105 MGI 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23035106 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180215 MGI PMID:27562646 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180215 MGI PMID:27562646 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:23035106 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:23035106 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20180215 MGI PMID:27562646 1558507 Tnik TRAF2 and NCK interacting kinase gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:23035106 1558508 Trmt2b TRM2 tRNA methyltransferase 2B gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1558510 Ints1 integrator complex subunit 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16807365 1558510 Ints1 integrator complex subunit 1 gene MP:0006204 embryonic lethality before implantation IEA N RGD:5509061 20111116 MGI 1558510 Ints1 integrator complex subunit 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16807365 1558515 Gdpd5 glycerophosphodiester phosphodiesterase domain containing 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20170105 MGI 1558515 Gdpd5 glycerophosphodiester phosphodiesterase domain containing 5 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21943603 1558515 Gdpd5 glycerophosphodiester phosphodiesterase domain containing 5 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:21943603 1558515 Gdpd5 glycerophosphodiester phosphodiesterase domain containing 5 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:21943603 1558515 Gdpd5 glycerophosphodiester phosphodiesterase domain containing 5 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20201022 MGI 1558515 Gdpd5 glycerophosphodiester phosphodiesterase domain containing 5 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21943603 1558515 Gdpd5 glycerophosphodiester phosphodiesterase domain containing 5 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1558515 Gdpd5 glycerophosphodiester phosphodiesterase domain containing 5 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1558517 Gpr150 G protein-coupled receptor 150 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 1558517 Gpr150 G protein-coupled receptor 150 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20240523 MGI 1558517 Gpr150 G protein-coupled receptor 150 gene MP:0010511 shortened PR interval IEA N RGD:5509061 20231207 MGI 1558520 Ubl4a ubiquitin-like 4A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161013 MGI PMID:26195787 1558520 Ubl4a ubiquitin-like 4A gene MP:0001575 cyanosis IAGP N RGD:5509061 20161013 MGI PMID:26195787 1558520 Ubl4a ubiquitin-like 4A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22139977 1558520 Ubl4a ubiquitin-like 4A gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20161013 MGI PMID:26195787 1558520 Ubl4a ubiquitin-like 4A gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20161013 MGI PMID:26195787 1558521 Gtf2h5 general transcription factor IIH, polypeptide 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23637614 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230601 MGI 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15319281 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20210128 MGI 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:15319281 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15319281 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210826 MGI 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15319281 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0002879 increased cellular sensitivity to X-ray irradiation IAGP N RGD:5509061 20141003 MGI PMID:15319281 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:15319281 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15319281 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:15319281 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15319281 1558522 Apex2 apurinic/apyrimidinic endonuclease 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:15319281 1558524 Ncapd2 non-SMC condensin I complex, subunit D2 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20221201 MGI PMID:34229059 1558524 Ncapd2 non-SMC condensin I complex, subunit D2 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20221201 MGI PMID:34229059 1558525 Osbpl8 oxysterol binding protein-like 8 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20230119 MGI 1558525 Osbpl8 oxysterol binding protein-like 8 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230119 MGI 1558525 Osbpl8 oxysterol binding protein-like 8 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1558525 Osbpl8 oxysterol binding protein-like 8 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230119 MGI 1558525 Osbpl8 oxysterol binding protein-like 8 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23554939 1558525 Osbpl8 oxysterol binding protein-like 8 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1558525 Osbpl8 oxysterol binding protein-like 8 gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:23554939 1558525 Osbpl8 oxysterol binding protein-like 8 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230119 MGI 1558525 Osbpl8 oxysterol binding protein-like 8 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23554939 1558525 Osbpl8 oxysterol binding protein-like 8 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230119 MGI 1558525 Osbpl8 oxysterol binding protein-like 8 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230119 MGI 1558525 Osbpl8 oxysterol binding protein-like 8 gene MP:0010332 abnormal circulating apolipoprotein level IAGP N RGD:5509061 20141003 MGI PMID:23554939 1558525 Osbpl8 oxysterol binding protein-like 8 gene MP:0010333 abnormal circulating apolipoprotein E level IAGP N RGD:5509061 20141003 MGI PMID:23554939 1558525 Osbpl8 oxysterol binding protein-like 8 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230119 MGI 1558526 Fzd8 frizzled class receptor 8 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:21343368 1558526 Fzd8 frizzled class receptor 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21343368 1558526 Fzd8 frizzled class receptor 8 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20190502 MGI 1558526 Fzd8 frizzled class receptor 8 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:21343368 1558526 Fzd8 frizzled class receptor 8 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:21343368 1558526 Fzd8 frizzled class receptor 8 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20190502 MGI 1558526 Fzd8 frizzled class receptor 8 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20210128 MGI 1558526 Fzd8 frizzled class receptor 8 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21343368 1558526 Fzd8 frizzled class receptor 8 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20211021 MGI 1558527 Prpf18 pre-mRNA processing factor 18 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558527 Prpf18 pre-mRNA processing factor 18 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1558527 Prpf18 pre-mRNA processing factor 18 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220519 MGI 1558528 Sdk2 sidekick cell adhesion molecule 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20151224 MGI PMID:26287463 1558529 Gpr143 G protein-coupled receptor 143 gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:11092754 1558529 Gpr143 G protein-coupled receptor 143 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:11092754 1558529 Gpr143 G protein-coupled receptor 143 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:11092754 1558529 Gpr143 G protein-coupled receptor 143 gene MP:0005101 abnormal ciliary body pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11092754 1558529 Gpr143 G protein-coupled receptor 143 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11092754 1558529 Gpr143 G protein-coupled receptor 143 gene MP:0005199 abnormal iris pigment epithelium IAGP N RGD:5509061 20141003 MGI PMID:11092754 1558529 Gpr143 G protein-coupled receptor 143 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11092754 1558530 Septin12 septin 12 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19359518 1558530 Septin12 septin 12 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19359518 1558530 Septin12 septin 12 gene MP:0001925 male infertility IAGP N RGD:5509061 20220811 MGI PMID:35547809 1558530 Septin12 septin 12 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220324 MGI PMID:25588830 1558530 Septin12 septin 12 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220714 MGI PMID:19359518 1558530 Septin12 septin 12 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220811 MGI PMID:35547809 1558530 Septin12 septin 12 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19359518 1558530 Septin12 septin 12 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220811 MGI PMID:35547809 1558530 Septin12 septin 12 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19359518 1558530 Septin12 septin 12 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220811 MGI PMID:35547809 1558530 Septin12 septin 12 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20220811 MGI PMID:35547809 1558530 Septin12 septin 12 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19359518 1558530 Septin12 septin 12 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:19359518 1558530 Septin12 septin 12 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220811 MGI PMID:35547809 1558530 Septin12 septin 12 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220811 MGI PMID:35547809 1558530 Septin12 septin 12 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19359518 1558530 Septin12 septin 12 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:19359518 1558530 Septin12 septin 12 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220324 MGI PMID:25588830 1558530 Septin12 septin 12 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:19359518 1558530 Septin12 septin 12 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:19359518 1558530 Septin12 septin 12 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20141003 MGI PMID:19359518 1558530 Septin12 septin 12 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19359518 1558530 Septin12 septin 12 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20220811 MGI PMID:35547809 1558530 Septin12 septin 12 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:19359518 1558530 Septin12 septin 12 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220324 MGI PMID:25588830 1558530 Septin12 septin 12 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220811 MGI PMID:35547809 1558530 Septin12 septin 12 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220811 MGI PMID:35547809 1558530 Septin12 septin 12 gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20220811 MGI PMID:35547809 1558530 Septin12 septin 12 gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20220324 MGI PMID:25588830 1558530 Septin12 septin 12 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19359518 1558530 Septin12 septin 12 gene MP:0031013 abnormal egg activation IAGP N RGD:5509061 20220811 MGI PMID:35547809 1558530 Septin12 septin 12 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220811 MGI PMID:35547809 1558531 Npm3 nucleoplasmin 3 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1558531 Npm3 nucleoplasmin 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170105 MGI 1558531 Npm3 nucleoplasmin 3 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20220519 MGI 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:4784576 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:12461648 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:4784576 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0000439 enlarged cranium IEA N RGD:5509061 20111116 MGI 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:18250199 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0000743 muscle spasm IEA N RGD:5509061 20111116 MGI 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:4732188 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0000825 dilated lateral ventricle IEA N RGD:5509061 20111116 MGI 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:18250199 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12461648 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:4784576 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20111116 MGI 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18250199 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0001867 rhinitis IEA N RGD:5509061 20111116 MGI 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:12461648 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:18250199 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18250199 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0001947 abnormal mucociliary clearance IAGP N RGD:5509061 20141003 MGI PMID:18250199 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0002061 abnormal aggression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:4784576 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20141003 MGI PMID:4784576 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18250199 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0002133 abnormal respiratory system physiology IEA N RGD:5509061 20111116 MGI 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0002653 abnormal ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:4784576 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:18250199 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0003644 thymus atrophy IEA N RGD:5509061 20111116 MGI 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0004421 enlarged parietal bone IEA N RGD:5509061 20111116 MGI 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0005150 cachexia IEA N RGD:5509061 20111116 MGI 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:18250199 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:4732188 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:4784576 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0009022 abnormal brain meninges morphology IEA N RGD:5509061 20111116 MGI 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0009804 abnormal brain interventricular foramen morphology IEA N RGD:5509061 20161103 MGI 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:18250199 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:18250199 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:18250199 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0011059 abnormal ependyma motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:18250199 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:18250199 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12461648 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:12461648 1558533 Hydin HYDIN, axonemal central pair apparatus protein gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:4784576 1558535 Hmgxb3 HMG box domain containing 3 gene MP:0000026 abnormal inner ear morphology IEA N RGD:5509061 20171228 MGI 1558535 Hmgxb3 HMG box domain containing 3 gene MP:0000914 exencephaly IEA N RGD:5509061 20171228 MGI 1558535 Hmgxb3 HMG box domain containing 3 gene MP:0002947 increased hemangioma incidence IEA N RGD:5509061 20210930 MGI 1558535 Hmgxb3 HMG box domain containing 3 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20171228 MGI 1558535 Hmgxb3 HMG box domain containing 3 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20171228 MGI 1558535 Hmgxb3 HMG box domain containing 3 gene MP:0004463 basisphenoid bone foramen IEA N RGD:5509061 20171228 MGI 1558535 Hmgxb3 HMG box domain containing 3 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20171228 MGI 1558535 Hmgxb3 HMG box domain containing 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558535 Hmgxb3 HMG box domain containing 3 gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20171228 MGI 1558535 Hmgxb3 HMG box domain containing 3 gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20171228 MGI 1558535 Hmgxb3 HMG box domain containing 3 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20171228 MGI 1558535 Hmgxb3 HMG box domain containing 3 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20171228 MGI 1558535 Hmgxb3 HMG box domain containing 3 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20171228 MGI 1558535 Hmgxb3 HMG box domain containing 3 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20171228 MGI 1558535 Hmgxb3 HMG box domain containing 3 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20171228 MGI 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200402 MGI PMID:30338217 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0000371 diluted coat color IAGP N RGD:5509061 20210121 MGI PMID:31399401 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20210121 MGI PMID:31399401 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200402 MGI PMID:26885862 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200402 MGI PMID:30338217 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200402 MGI PMID:30338217 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0004721 abnormal platelet dense granule morphology IAGP N RGD:5509061 20210121 MGI PMID:31399401 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20210121 MGI PMID:31399401 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20210121 MGI PMID:31399401 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20210121 MGI PMID:31399401 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20200402 MGI PMID:30338217 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20210121 MGI PMID:31399401 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20210121 MGI PMID:31399401 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0009557 decreased platelet ADP level IAGP N RGD:5509061 20210121 MGI PMID:31399401 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0009709 hydrometra IEA N RGD:5509061 20170105 MGI 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0010052 increased grip strength IEA N RGD:5509061 20231207 MGI 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0010815 enlarged alveolar lamellar bodies IAGP N RGD:5509061 20210121 MGI PMID:31399401 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0010911 abnormal pulmonary acinus morphology IAGP N RGD:5509061 20210121 MGI PMID:31399401 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20200402 MGI PMID:30338217 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0013956 decreased colon length IAGP N RGD:5509061 20200402 MGI PMID:30338217 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20210121 MGI PMID:31399401 1558536 Rab32 RAB32, member RAS oncogene family gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20210121 MGI PMID:31399401 1558537 Kif17 kinesin family member 17 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:21521616 1558537 Kif17 kinesin family member 17 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21521616 1558537 Kif17 kinesin family member 17 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:21521616 1558537 Kif17 kinesin family member 17 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:21521616 1558537 Kif17 kinesin family member 17 gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21521616 1558537 Kif17 kinesin family member 17 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:21521616 1558537 Kif17 kinesin family member 17 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21521616 1558537 Kif17 kinesin family member 17 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:21521616 1558540 Nop53 NOP53 ribosome biogenesis factor gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20170817 MGI PMID:21804542 1558540 Nop53 NOP53 ribosome biogenesis factor gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20170817 MGI PMID:21804542 1558540 Nop53 NOP53 ribosome biogenesis factor gene MP:0020438 decreased papilloma incidence IAGP N RGD:5509061 20170831 MGI PMID:21804542 1558541 Septin11 septin 11 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1558541 Septin11 septin 11 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200409 MGI PMID:21824005 1558541 Septin11 septin 11 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200409 MGI PMID:21824005 1558541 Septin11 septin 11 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200514 MGI 1558541 Septin11 septin 11 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1558542 Zfyve16 zinc finger, FYVE domain containing 16 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20210415 MGI PMID:29247407 1558542 Zfyve16 zinc finger, FYVE domain containing 16 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20210415 MGI PMID:29247407 1558542 Zfyve16 zinc finger, FYVE domain containing 16 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20210415 MGI PMID:29247407 1558542 Zfyve16 zinc finger, FYVE domain containing 16 gene MP:0013892 increased common lymphocyte progenitor cell number IAGP N RGD:5509061 20210415 MGI PMID:29247407 1558543 Pla2r1 phospholipase A2 receptor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20211223 MGI PMID:33594040 1558543 Pla2r1 phospholipase A2 receptor 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:9407054 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20221215 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20211021 MGI PMID:32376790 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20211021 MGI PMID:32376790 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20211021 MGI PMID:32376790 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20211021 MGI PMID:32376790 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20221215 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20211021 MGI PMID:32376790 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1558544 Bcorl1 BCL6 co-repressor-like 1 gene MP:0030610 absent teeth IEA N RGD:5509061 20240523 MGI 1558545 Pla2g12b phospholipase A2, group XIIB gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20160929 MGI PMID:27534441 1558545 Pla2g12b phospholipase A2, group XIIB gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22912808 1558545 Pla2g12b phospholipase A2, group XIIB gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20160929 MGI PMID:27534441 1558545 Pla2g12b phospholipase A2, group XIIB gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:22912808 1558545 Pla2g12b phospholipase A2, group XIIB gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22912808 1558545 Pla2g12b phospholipase A2, group XIIB gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22912808 1558547 Cramp1 cramped chromatin regulator 1 gene MP:0000111 cleft palate IEA N RGD:5509061 20111116 MGI 1558547 Cramp1 cramped chromatin regulator 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20220519 MGI 1558547 Cramp1 cramped chromatin regulator 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220519 MGI 1558547 Cramp1 cramped chromatin regulator 1 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20220519 MGI 1558547 Cramp1 cramped chromatin regulator 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220519 MGI 1558547 Cramp1 cramped chromatin regulator 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220519 MGI 1558547 Cramp1 cramped chromatin regulator 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1558548 Wac WW domain containing adaptor with coiled-coil gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20181227 MGI 1558548 Wac WW domain containing adaptor with coiled-coil gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20210520 MGI 1558548 Wac WW domain containing adaptor with coiled-coil gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1558548 Wac WW domain containing adaptor with coiled-coil gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1558548 Wac WW domain containing adaptor with coiled-coil gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1558548 Wac WW domain containing adaptor with coiled-coil gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20210520 MGI 1558548 Wac WW domain containing adaptor with coiled-coil gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20201022 MGI 1558548 Wac WW domain containing adaptor with coiled-coil gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20181227 MGI 1558548 Wac WW domain containing adaptor with coiled-coil gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558548 Wac WW domain containing adaptor with coiled-coil gene MP:0013025 increased Ly6C low monocyte number IEA N RGD:5509061 20181227 MGI 1558549 Megf10 multiple EGF-like-domains 10 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20160929 MGI PMID:27170117 1558549 Megf10 multiple EGF-like-domains 10 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22407321 1558549 Megf10 multiple EGF-like-domains 10 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22407321 1558549 Megf10 multiple EGF-like-domains 10 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20160929 MGI PMID:27170117 1558549 Megf10 multiple EGF-like-domains 10 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20160929 MGI PMID:27170117 1558550 Ptms parathymosin gene MP:0001399 hyperactivity IEA N RGD:5509061 20170105 MGI 1558550 Ptms parathymosin gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1558550 Ptms parathymosin gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1558550 Ptms parathymosin gene MP:0004924 abnormal behavior IEA N RGD:5509061 20170105 MGI 1558550 Ptms parathymosin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558550 Ptms parathymosin gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20240523 MGI 1558550 Ptms parathymosin gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1558551 Dtna dystrobrevin alpha gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10559919 1558551 Dtna dystrobrevin alpha gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:10559919 1558551 Dtna dystrobrevin alpha gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:10719885 1558551 Dtna dystrobrevin alpha gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:10719885 1558551 Dtna dystrobrevin alpha gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16540561 1558551 Dtna dystrobrevin alpha gene MP:0001405 impaired coordination IAGP N RGD:5509061 20240215 MGI PMID:37461313 1558551 Dtna dystrobrevin alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10559919 1558551 Dtna dystrobrevin alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10559919 1558551 Dtna dystrobrevin alpha gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:10559919 1558551 Dtna dystrobrevin alpha gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10559919 1558551 Dtna dystrobrevin alpha gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:10559919 1558551 Dtna dystrobrevin alpha gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:10559919 1558551 Dtna dystrobrevin alpha gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:16540561 1558551 Dtna dystrobrevin alpha gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:10559919 1558551 Dtna dystrobrevin alpha gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16540561 1558551 Dtna dystrobrevin alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10559919 1558552 Pdcl2 phosducin-like 2 gene MP:0001147 small testis IAGP N RGD:5509061 20231116 MGI PMID:36278277 1558552 Pdcl2 phosducin-like 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20231116 MGI PMID:36278277 1558552 Pdcl2 phosducin-like 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20231116 MGI PMID:36278277 1558552 Pdcl2 phosducin-like 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20231116 MGI PMID:36278277 1558552 Pdcl2 phosducin-like 2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20231116 MGI PMID:36278277 1558552 Pdcl2 phosducin-like 2 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20231116 MGI PMID:36278277 1558552 Pdcl2 phosducin-like 2 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20231116 MGI PMID:36278277 1558552 Pdcl2 phosducin-like 2 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20231116 MGI PMID:36278277 1558552 Pdcl2 phosducin-like 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20231116 MGI PMID:36278277 1558552 Pdcl2 phosducin-like 2 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20231116 MGI PMID:36278277 1558552 Pdcl2 phosducin-like 2 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20231116 MGI PMID:36278277 1558552 Pdcl2 phosducin-like 2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20231116 MGI PMID:36278277 1558552 Pdcl2 phosducin-like 2 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20231116 MGI PMID:36278277 1558552 Pdcl2 phosducin-like 2 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20231116 MGI PMID:36278277 1558552 Pdcl2 phosducin-like 2 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20231116 MGI PMID:36278277 1558553 Acer3 alkaline ceramidase 3 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20180301 MGI PMID:26474409 1558553 Acer3 alkaline ceramidase 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180301 MGI PMID:26474409 1558553 Acer3 alkaline ceramidase 3 gene MP:0001513 limb grasping IAGP N RGD:5509061 20180301 MGI PMID:26474409 1558553 Acer3 alkaline ceramidase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180301 MGI PMID:29401619 1558553 Acer3 alkaline ceramidase 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20180301 MGI PMID:26474409 1558553 Acer3 alkaline ceramidase 3 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20180301 MGI PMID:26474409 1558553 Acer3 alkaline ceramidase 3 gene MP:0012230 abnormal sphingolipid level IAGP N RGD:5509061 20180301 MGI PMID:26474409 1558553 Acer3 alkaline ceramidase 3 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20180301 MGI PMID:26474409 1558553 Acer3 alkaline ceramidase 3 gene MP:0020116 increased sphingosine level IAGP N RGD:5509061 20180301 MGI PMID:26474409 1558556 Suv39h1 suppressor of variegation 3-9 1 gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:11701123 1558556 Suv39h1 suppressor of variegation 3-9 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11701123 1558556 Suv39h1 suppressor of variegation 3-9 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11701123 1558556 Suv39h1 suppressor of variegation 3-9 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:11701123 1558556 Suv39h1 suppressor of variegation 3-9 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11701123 1558556 Suv39h1 suppressor of variegation 3-9 1 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:22763435 1558556 Suv39h1 suppressor of variegation 3-9 1 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:22763435 1558556 Suv39h1 suppressor of variegation 3-9 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:11701123 1558556 Suv39h1 suppressor of variegation 3-9 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11701123 1558557 Tmbim1 transmembrane BAX inhibitor motif containing 1 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:16636500 1558557 Tmbim1 transmembrane BAX inhibitor motif containing 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16636500 1558557 Tmbim1 transmembrane BAX inhibitor motif containing 1 gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:16607040 1558557 Tmbim1 transmembrane BAX inhibitor motif containing 1 gene MP:0010574 dilated aorta IAGP N RGD:5509061 20141003 MGI PMID:16636500 1558558 Rbm6 RNA binding motif protein 6 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1558558 Rbm6 RNA binding motif protein 6 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 1558558 Rbm6 RNA binding motif protein 6 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1558558 Rbm6 RNA binding motif protein 6 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1558558 Rbm6 RNA binding motif protein 6 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1558558 Rbm6 RNA binding motif protein 6 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17159984 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:20062524 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17159984 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:22038916 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17159982 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17486093 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17159982 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17159984 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20062524 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17159984 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17159982 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17159984 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:17159984 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0004880 lung cyst IAGP N RGD:5509061 20141003 MGI PMID:17159982 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:17159982 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:17159984 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:20062524 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:22038916 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20062524 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20141003 MGI PMID:22038916 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0008615 decreased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:22038916 1558559 Clec7a C-type lectin domain family 7, member a gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17159984 1558560 Tas2r138 taste receptor, type 2, member 138 gene MP:0001513 limb grasping IEA N RGD:5509061 20201231 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20151224 MGI PMID:24509510 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12479824 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16968900 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16968900 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:16968900 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0001655 multifocal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12479824 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16968900 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12479824 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16968900 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20151224 MGI PMID:24509509 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20151224 MGI PMID:24509510 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16968900 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11870616 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12479824 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20151224 MGI PMID:24509509 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12479824 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002343 abnormal lymph node cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002348 abnormal lymph node medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002367 abnormal thymus lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:12479824 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20151224 MGI PMID:24509509 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20151224 MGI PMID:24509510 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002493 increased IgG level IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002606 increased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0003133 increased early pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12479824 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12479824 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005015 increased T cell number IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11870616 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005061 abnormal eosinophil morphology IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005068 abnormal NK cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16968900 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11870616 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0005461 abnormal dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12479824 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008046 absent NK cells IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008046 absent NK cells IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008082 increased single-positive T cell number IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008083 decreased single-positive T cell number IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008125 abnormal dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:11870616 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008170 decreased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:11870616 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008170 decreased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12479824 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20151224 MGI PMID:24509509 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008187 absent pro-B cells IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008187 absent pro-B cells IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008203 absent B-1a cells IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20151224 MGI PMID:24509509 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20151224 MGI PMID:24509509 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20151224 MGI PMID:24509510 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:11870616 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008354 decreased mature gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008463 abnormal peripheral lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008465 absent mesenteric lymph nodes IAGP N RGD:5509061 20170713 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008465 absent mesenteric lymph nodes IAGP N RGD:5509061 20170713 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:11870616 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11870616 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008542 enlarged cervical lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7585946 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:18538592 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008781 abnormal B cell apoptosis IAGP N RGD:5509061 20151224 MGI PMID:24509510 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0009633 absent cervical lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0009633 absent cervical lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8986714 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0010130 decreased DN1 thymic pro-T cell number IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0010132 decreased DN2 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0010134 decreased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:20393504 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7923373 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0011176 abnormal erythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0011243 decreased fetal derived definitive erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12871645 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0011719 abnormal natural killer cell mediated cytotoxicity IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0011816 decreased pre-pro B cell number IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16968900 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24013668 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0014472 impaired B cell migration IAGP N RGD:5509061 20240613 MGI PMID:24509510 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0020002 increased response to antigen IEA N RGD:5509061 20181011 MGI 1558562 Ikzf1 IKAROS family zinc finger 1 gene MP:0020155 enhanced humoral immune response IEA N RGD:5509061 20181011 MGI 1558563 Atg12 autophagy related 12 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:25585051 1558563 Atg12 autophagy related 12 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:25585051 1558563 Atg12 autophagy related 12 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:25585051 1558563 Atg12 autophagy related 12 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:25585051 1558563 Atg12 autophagy related 12 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20200310 MGI PMID:25585051 1558563 Atg12 autophagy related 12 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:25585051 1558563 Atg12 autophagy related 12 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25585051 1558563 Atg12 autophagy related 12 gene MP:0011939 increased food intake IAGP N RGD:5509061 20200310 MGI PMID:25585051 1558563 Atg12 autophagy related 12 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20200310 MGI PMID:25585051 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:10631181 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10631181 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20230831 MGI 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0000601 small liver IEA N RGD:5509061 20230601 MGI 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20230601 MGI 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:15673568 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:15673568 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20230601 MGI 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:15673568 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20231207 MGI 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:11416163 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11416163 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16179923 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:10631181 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10631181 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10631181 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:10631181 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:12654290 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10631181 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10631181 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0004635 short metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0004639 fused metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0004642 fused metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:10631181 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0004642 fused metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15673568 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:10631181 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10631181 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12654290 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15673568 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0008258 thin endometrium IAGP N RGD:5509061 20141003 MGI PMID:11416163 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20230601 MGI 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0008275 failure of endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:11416163 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0009097 absent endometrial glands IAGP N RGD:5509061 20141003 MGI PMID:11416163 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16179923 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0009374 absent cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:11416163 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0009728 abnormal calcaneum morphology IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0012281 decreased sternebra size IAGP N RGD:5509061 20141003 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0013400 abnormal endometrial gland development IAGP N RGD:5509061 20141218 MGI PMID:11416163 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:15781876 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0014291 decreased autopod size IAGP N RGD:5509061 20230824 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:12654290 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:15673568 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0030843 elbow dislocation IAGP N RGD:5509061 20181025 MGI PMID:10631182 1558564 Bmpr1b bone morphogenetic protein receptor, type 1B gene MP:0030886 decreased radius size IAGP N RGD:5509061 20181101 MGI PMID:15781876 1558565 Elmod3 ELMO/CED-12 domain containing 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201001 MGI PMID:31628468 1558565 Elmod3 ELMO/CED-12 domain containing 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1558565 Elmod3 ELMO/CED-12 domain containing 3 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20201001 MGI PMID:31628468 1558565 Elmod3 ELMO/CED-12 domain containing 3 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20201001 MGI PMID:31628468 1558565 Elmod3 ELMO/CED-12 domain containing 3 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20201001 MGI PMID:31628468 1558565 Elmod3 ELMO/CED-12 domain containing 3 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20201001 MGI PMID:31628468 1558565 Elmod3 ELMO/CED-12 domain containing 3 gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20201001 MGI PMID:31628468 1558565 Elmod3 ELMO/CED-12 domain containing 3 gene MP:0004536 short inner hair cell stereocilia IAGP N RGD:5509061 20201001 MGI PMID:31628468 1558565 Elmod3 ELMO/CED-12 domain containing 3 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20201001 MGI PMID:31628468 1558565 Elmod3 ELMO/CED-12 domain containing 3 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20201001 MGI PMID:31628468 1558565 Elmod3 ELMO/CED-12 domain containing 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20201001 MGI PMID:31628468 1558565 Elmod3 ELMO/CED-12 domain containing 3 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20201001 MGI PMID:31628468 1558566 Spen spen family transcription repressor gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12594956 1558566 Spen spen family transcription repressor gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12594956 1558566 Spen spen family transcription repressor gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:12594956 1558566 Spen spen family transcription repressor gene MP:0000771 abnormal brain size IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:12594956 1558566 Spen spen family transcription repressor gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12594956 1558566 Spen spen family transcription repressor gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:12594956 1558566 Spen spen family transcription repressor gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17457934 1558566 Spen spen family transcription repressor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12594956 1558567 Ppef1 protein phosphatase with EF hand calcium-binding domain 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11713293 1558568 Maco1 macoilin 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1558572 Tubb2a tubulin, beta 2A class IIA gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1558572 Tubb2a tubulin, beta 2A class IIA gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20210304 MGI PMID:31386652 1558572 Tubb2a tubulin, beta 2A class IIA gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20210304 MGI PMID:31386652 1558572 Tubb2a tubulin, beta 2A class IIA gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1558572 Tubb2a tubulin, beta 2A class IIA gene MP:0001406 abnormal gait IEA N RGD:5509061 20240523 MGI 1558572 Tubb2a tubulin, beta 2A class IIA gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1558572 Tubb2a tubulin, beta 2A class IIA gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1558572 Tubb2a tubulin, beta 2A class IIA gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20210304 MGI PMID:31386652 1558572 Tubb2a tubulin, beta 2A class IIA gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1558572 Tubb2a tubulin, beta 2A class IIA gene MP:0012448 abnormal primary motor cortex morphology IAGP N RGD:5509061 20210304 MGI PMID:31386652 1558574 Lamb3 laminin, beta 3 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9271670 1558574 Lamb3 laminin, beta 3 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:9271670 1558574 Lamb3 laminin, beta 3 gene MP:0001208 blistering IAGP N RGD:5509061 20160304 MGI PMID:25350318 1558574 Lamb3 laminin, beta 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160304 MGI PMID:25350318 1558574 Lamb3 laminin, beta 3 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20160304 MGI PMID:25350318 1558574 Lamb3 laminin, beta 3 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20160421 MGI 1558574 Lamb3 laminin, beta 3 gene MP:0002251 abnormal nasopharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:9271670 1558574 Lamb3 laminin, beta 3 gene MP:0002252 abnormal oropharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:9271670 1558574 Lamb3 laminin, beta 3 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20160304 MGI PMID:25350318 1558574 Lamb3 laminin, beta 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160304 MGI PMID:25350318 1558574 Lamb3 laminin, beta 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9271670 1558574 Lamb3 laminin, beta 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20160304 MGI PMID:25350318 1558574 Lamb3 laminin, beta 3 gene MP:0011159 abnormal epidermal-dermal junction morphology IAGP N RGD:5509061 20160304 MGI PMID:25350318 1558574 Lamb3 laminin, beta 3 gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20141003 MGI PMID:9271670 1558576 Zfhx2 zinc finger homeobox 2 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20220519 MGI 1558576 Zfhx2 zinc finger homeobox 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1558576 Zfhx2 zinc finger homeobox 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20220901 MGI PMID:29253101 1558576 Zfhx2 zinc finger homeobox 2 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20220519 MGI 1558576 Zfhx2 zinc finger homeobox 2 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20220901 MGI PMID:29253101 1558576 Zfhx2 zinc finger homeobox 2 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20220519 MGI 1558576 Zfhx2 zinc finger homeobox 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20221215 MGI 1558576 Zfhx2 zinc finger homeobox 2 gene MP:0020955 increased mechanical nociceptive threshold IAGP N RGD:5509061 20220901 MGI PMID:29253101 1558577 Irx6 Iroquois homeobox 6 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20200402 MGI 1558577 Irx6 Iroquois homeobox 6 gene MP:0001257 increased body length IEA N RGD:5509061 20240523 MGI 1558577 Irx6 Iroquois homeobox 6 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1558577 Irx6 Iroquois homeobox 6 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20200402 MGI 1558577 Irx6 Iroquois homeobox 6 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200402 MGI 1558577 Irx6 Iroquois homeobox 6 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20190808 MGI 1558577 Irx6 Iroquois homeobox 6 gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23172916 1558577 Irx6 Iroquois homeobox 6 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23172916 1558577 Irx6 Iroquois homeobox 6 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23172916 1558577 Irx6 Iroquois homeobox 6 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23172916 1558577 Irx6 Iroquois homeobox 6 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20201231 MGI 1558580 Ubp1 upstream binding protein 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20200402 MGI 1558580 Ubp1 upstream binding protein 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15282311 1558580 Ubp1 upstream binding protein 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15282311 1558580 Ubp1 upstream binding protein 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:15282311 1558580 Ubp1 upstream binding protein 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15282311 1558580 Ubp1 upstream binding protein 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200402 MGI 1558580 Ubp1 upstream binding protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15282311 1558580 Ubp1 upstream binding protein 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:15282311 1558580 Ubp1 upstream binding protein 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:15282311 1558580 Ubp1 upstream binding protein 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:15282311 1558580 Ubp1 upstream binding protein 1 gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1558580 Ubp1 upstream binding protein 1 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:15282311 1558580 Ubp1 upstream binding protein 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15282311 1558580 Ubp1 upstream binding protein 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:15282311 1558580 Ubp1 upstream binding protein 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20200402 MGI 1558580 Ubp1 upstream binding protein 1 gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1558580 Ubp1 upstream binding protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15282311 1558580 Ubp1 upstream binding protein 1 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:15282311 1558580 Ubp1 upstream binding protein 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210520 MGI 1558580 Ubp1 upstream binding protein 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1558580 Ubp1 upstream binding protein 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15282311 1558580 Ubp1 upstream binding protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15282311 1558580 Ubp1 upstream binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558580 Ubp1 upstream binding protein 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1558585 Cbx2 chromobox 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:9641679 1558585 Cbx2 chromobox 2 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:9043087 1558585 Cbx2 chromobox 2 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:9641679 1558585 Cbx2 chromobox 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:9641679 1558585 Cbx2 chromobox 2 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:9043087 1558585 Cbx2 chromobox 2 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:9641679 1558585 Cbx2 chromobox 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20160421 MGI 1558585 Cbx2 chromobox 2 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9043087 1558585 Cbx2 chromobox 2 gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:9641679 1558585 Cbx2 chromobox 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9043087 1558585 Cbx2 chromobox 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9641679 1558585 Cbx2 chromobox 2 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:9641679 1558585 Cbx2 chromobox 2 gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:9641679 1558585 Cbx2 chromobox 2 gene MP:0002213 true hermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:9641679 1558585 Cbx2 chromobox 2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9043087 1558585 Cbx2 chromobox 2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9641679 1558585 Cbx2 chromobox 2 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:9043087 1558585 Cbx2 chromobox 2 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:9043087 1558585 Cbx2 chromobox 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9043087 1558585 Cbx2 chromobox 2 gene MP:0005644 agonadal IAGP N RGD:5509061 20141003 MGI PMID:9641679 1558585 Cbx2 chromobox 2 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:9043087 1558585 Cbx2 chromobox 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1558585 Cbx2 chromobox 2 gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20141003 MGI PMID:9043087 1558585 Cbx2 chromobox 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9043087 1558585 Cbx2 chromobox 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9641679 1558585 Cbx2 chromobox 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9043087 1558585 Cbx2 chromobox 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558585 Cbx2 chromobox 2 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:9043087 1558585 Cbx2 chromobox 2 gene MP:0012283 decreased sternebra number IAGP N RGD:5509061 20141003 MGI PMID:9043087 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000111 cleft palate IEA N RGD:5509061 20210520 MGI 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:17360769 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:17360769 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:22007134 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:17360769 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:17360769 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:22007134 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17360769 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:22007134 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:17360769 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:22007134 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:17360769 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20210520 MGI 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0004096 abnormal midbrain-hindbrain boundary development IAGP N RGD:5509061 20141003 MGI PMID:17360769 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0004309 absent otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:22007134 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0006198 enophthalmos IAGP N RGD:5509061 20171019 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0006292 abnormal nasal placode morphology IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0006306 abnormal nasal pit morphology IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0008219 abnormal dorsal telencephalic commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20160526 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141218 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141218 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0008797 facial cleft IEA N RGD:5509061 20210520 MGI 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0010059 olfactory bulb hypoplasia IAGP N RGD:5509061 20171019 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17360769 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17360769 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0011495 abnormal head shape IEA N RGD:5509061 20210520 MGI 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0011759 absent Rathke's pouch IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0012004 abnormal septum pellucidum morphology IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:17360769 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:22007134 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0012178 absent frontonasal prominence IAGP N RGD:5509061 20171019 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0013342 bifurcated Rathke's pouch IAGP N RGD:5509061 20141204 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0013356 ectopic pituitary gland IAGP N RGD:5509061 20141218 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0013357 ectopic adenohypophysis IAGP N RGD:5509061 20141218 MGI PMID:19093031 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0013597 small vomeronasal organ IAGP N RGD:5509061 20150319 MGI PMID:9620767 1558586 Hesx1 homeobox gene expressed in ES cells gene MP:0014198 absent pituitary infundibular stalk IAGP N RGD:5509061 20160526 MGI PMID:9620767 1558587 Gdf2 growth differentiation factor 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1558587 Gdf2 growth differentiation factor 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558587 Gdf2 growth differentiation factor 2 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558587 Gdf2 growth differentiation factor 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1558587 Gdf2 growth differentiation factor 2 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22566602 1558587 Gdf2 growth differentiation factor 2 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558587 Gdf2 growth differentiation factor 2 gene MP:0004038 lymphangiectasis IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558587 Gdf2 growth differentiation factor 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22566602 1558587 Gdf2 growth differentiation factor 2 gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20141003 MGI PMID:22566602 1558587 Gdf2 growth differentiation factor 2 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558587 Gdf2 growth differentiation factor 2 gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558588 Timm17b translocase of inner mitochondrial membrane 17b gene MP:0005505 thrombocytosis IEA N RGD:5509061 20240523 MGI 1558588 Timm17b translocase of inner mitochondrial membrane 17b gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1558589 Actrt1 actin-related protein T1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20211021 MGI PMID:34422805 1558589 Actrt1 actin-related protein T1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20211021 MGI PMID:34422805 1558589 Actrt1 actin-related protein T1 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20211021 MGI PMID:34422805 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160526 MGI PMID:24928897 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0001297 microphthalmia IEA N RGD:5509061 20210128 MGI 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20150924 MGI PMID:20203623 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0001525 impaired balance IAGP N RGD:5509061 20150924 MGI PMID:20203623 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20150924 MGI PMID:20203623 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20150924 MGI PMID:20203623 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20150924 MGI PMID:20203623 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20150924 MGI PMID:20203623 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0004793 abnormal synaptic vesicle clustering IAGP N RGD:5509061 20150924 MGI PMID:20203623 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20210128 MGI 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0006320 abnormal interscapular fat pad morphology IAGP N RGD:5509061 20160526 MGI PMID:24928897 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20160526 MGI PMID:24928897 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20160526 MGI PMID:24928897 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20160526 MGI PMID:24928897 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20160526 MGI PMID:24928897 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20160526 MGI PMID:24928897 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20160526 MGI PMID:24928897 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20150924 MGI PMID:20203623 1558591 Ap1s2 adaptor-related protein complex 1, sigma 2 subunit gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1558593 Cxcl16 C-X-C motif chemokine ligand 16 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18056360 1558593 Cxcl16 C-X-C motif chemokine ligand 16 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:18056360 1558593 Cxcl16 C-X-C motif chemokine ligand 16 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:18056360 1558593 Cxcl16 C-X-C motif chemokine ligand 16 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18056360 1558593 Cxcl16 C-X-C motif chemokine ligand 16 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:18056360 1558593 Cxcl16 C-X-C motif chemokine ligand 16 gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:18056360 1558593 Cxcl16 C-X-C motif chemokine ligand 16 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:18056360 1558593 Cxcl16 C-X-C motif chemokine ligand 16 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18056360 1558594 Lbx1 ladybird homeobox 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12522123 1558594 Lbx1 ladybird homeobox 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:12522123 1558594 Lbx1 ladybird homeobox 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10508520 1558594 Lbx1 ladybird homeobox 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10603357 1558594 Lbx1 ladybird homeobox 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10508520 1558594 Lbx1 ladybird homeobox 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10603357 1558594 Lbx1 ladybird homeobox 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:10603357 1558594 Lbx1 ladybird homeobox 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:10508520 1558594 Lbx1 ladybird homeobox 1 gene MP:0000756 forelimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:10508520 1558594 Lbx1 ladybird homeobox 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15653949 1558594 Lbx1 ladybird homeobox 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21956886 1558594 Lbx1 ladybird homeobox 1 gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20141003 MGI PMID:17475798 1558594 Lbx1 ladybird homeobox 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:12358782 1558594 Lbx1 ladybird homeobox 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20220519 MGI PMID:34906895 1558594 Lbx1 ladybird homeobox 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20220519 MGI PMID:34906895 1558594 Lbx1 ladybird homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21956886 1558594 Lbx1 ladybird homeobox 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12522123 1558594 Lbx1 ladybird homeobox 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12358782 1558594 Lbx1 ladybird homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21956886 1558594 Lbx1 ladybird homeobox 1 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20220519 MGI PMID:34906895 1558594 Lbx1 ladybird homeobox 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20220519 MGI PMID:34906895 1558594 Lbx1 ladybird homeobox 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17475798 1558594 Lbx1 ladybird homeobox 1 gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:17475798 1558594 Lbx1 ladybird homeobox 1 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:12522123 1558594 Lbx1 ladybird homeobox 1 gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:10508520 1558594 Lbx1 ladybird homeobox 1 gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:10603357 1558594 Lbx1 ladybird homeobox 1 gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:21956886 1558594 Lbx1 ladybird homeobox 1 gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16234809 1558594 Lbx1 ladybird homeobox 1 gene MP:0003247 abnormal glutaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16234809 1558594 Lbx1 ladybird homeobox 1 gene MP:0003994 abnormal dorsal spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:12358782 1558594 Lbx1 ladybird homeobox 1 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20220519 MGI PMID:34906895 1558594 Lbx1 ladybird homeobox 1 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20220519 MGI PMID:34906895 1558594 Lbx1 ladybird homeobox 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:10603357 1558594 Lbx1 ladybird homeobox 1 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:17475798 1558594 Lbx1 ladybird homeobox 1 gene MP:0006006 increased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:17475798 1558594 Lbx1 ladybird homeobox 1 gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:12358782 1558594 Lbx1 ladybird homeobox 1 gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20220519 MGI PMID:34906895 1558594 Lbx1 ladybird homeobox 1 gene MP:0006284 absent hypaxial muscle IAGP N RGD:5509061 20141003 MGI PMID:10603357 1558594 Lbx1 ladybird homeobox 1 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20220519 MGI PMID:34906895 1558594 Lbx1 ladybird homeobox 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20220519 MGI PMID:34906895 1558594 Lbx1 ladybird homeobox 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15769945 1558594 Lbx1 ladybird homeobox 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17475798 1558594 Lbx1 ladybird homeobox 1 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12522123 1558594 Lbx1 ladybird homeobox 1 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:12522123 1558594 Lbx1 ladybird homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21956886 1558594 Lbx1 ladybird homeobox 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10603357 1558594 Lbx1 ladybird homeobox 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20220519 MGI PMID:34906895 1558594 Lbx1 ladybird homeobox 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12522123 1558594 Lbx1 ladybird homeobox 1 gene MP:0021094 abnormal dorsal interneuron 3 morphology IAGP N RGD:5509061 20220519 MGI PMID:34906895 1558594 Lbx1 ladybird homeobox 1 gene MP:0021095 abnormal dorsal interneuron 4 morphology IAGP N RGD:5509061 20220519 MGI PMID:34906895 1558594 Lbx1 ladybird homeobox 1 gene MP:0021096 abnormal dorsal interneuron 5 morphology IAGP N RGD:5509061 20220519 MGI PMID:34906895 1558594 Lbx1 ladybird homeobox 1 gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:34906895 1558594 Lbx1 ladybird homeobox 1 gene MP:0021206 abnormal limb muscle morphology IAGP N RGD:5509061 20221201 MGI PMID:10508520 1558594 Lbx1 ladybird homeobox 1 gene MP:0021206 abnormal limb muscle morphology IAGP N RGD:5509061 20221201 MGI PMID:10603357 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0001926 female infertility IAGP N RGD:5509061 20240502 MGI PMID:38546043 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20240502 MGI PMID:32814047 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20240502 MGI PMID:38546043 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20240829 MGI PMID:36548081 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20240502 MGI PMID:32814047 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20240502 MGI PMID:32814047 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0008573 increased circulating interferon-alpha level IAGP N RGD:5509061 20240502 MGI PMID:32814047 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20240502 MGI PMID:32814047 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20240502 MGI PMID:32814047 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20240502 MGI PMID:38546043 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20240829 MGI PMID:36548081 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0014435 increased interferon level IAGP N RGD:5509061 20240502 MGI PMID:32814047 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20240502 MGI PMID:32814047 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20240502 MGI PMID:32814047 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0020938 decreased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20240502 MGI PMID:32814047 1558595 Ube2s ubiquitin-conjugating enzyme E2S gene MP:0031039 decreased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20240502 MGI PMID:32814047 1558597 Phb2 prohibitin 2 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20200310 MGI PMID:21862609 1558597 Phb2 prohibitin 2 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20200310 MGI PMID:15713652 1558597 Phb2 prohibitin 2 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20200310 MGI PMID:21862609 1558597 Phb2 prohibitin 2 gene MP:0001933 abnormal litter size IAGP N RGD:5509061 20200310 MGI PMID:15713652 1558597 Phb2 prohibitin 2 gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20200310 MGI PMID:21862609 1558597 Phb2 prohibitin 2 gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20200310 MGI PMID:15713652 1558597 Phb2 prohibitin 2 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20200310 MGI PMID:15713652 1558597 Phb2 prohibitin 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20200310 MGI PMID:18281461 1558597 Phb2 prohibitin 2 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20200310 MGI PMID:21862609 1558597 Phb2 prohibitin 2 gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20200310 MGI PMID:21862609 1558597 Phb2 prohibitin 2 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20200310 MGI PMID:18281461 1558597 Phb2 prohibitin 2 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20200310 MGI PMID:21862609 1558597 Phb2 prohibitin 2 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20200310 MGI PMID:21862609 1558597 Phb2 prohibitin 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15713652 1558597 Phb2 prohibitin 2 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18281461 1558597 Phb2 prohibitin 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15713652 1558597 Phb2 prohibitin 2 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:18281461 1558597 Phb2 prohibitin 2 gene MP:0014126 increased mammary gland apoptosis IAGP N RGD:5509061 20200310 MGI PMID:21862609 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15690081 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21407177 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:21407177 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15690081 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19805353 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:19805353 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18286202 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15690081 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21407177 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:21407177 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:24089213 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18286202 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:15690081 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21407177 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15690081 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:19805353 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0004264 abnormal extraembryonic tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:19805353 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0004265 abnormal placental transport IAGP N RGD:5509061 20141003 MGI PMID:19805353 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19805353 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21407177 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0005432 abnormal pro-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15690081 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17765679 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19805353 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21407177 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0010331 abnormal apolipoprotein level IAGP N RGD:5509061 20141003 MGI PMID:21407177 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10650002 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15690081 1558600 Ern1 endoplasmic reticulum to nucleus signalling 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19805353 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20180705 MGI PMID:29666258 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0000914 exencephaly IAGP N RGD:5509061 20180705 MGI PMID:29666258 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0000914 exencephaly IAGP N RGD:5509061 20230907 MGI PMID:35727412 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20180705 MGI PMID:29666258 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0000929 open neural tube IAGP N RGD:5509061 20180705 MGI PMID:29666258 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20230907 MGI PMID:35727412 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20230907 MGI PMID:35727412 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20230907 MGI PMID:35727412 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20180705 MGI PMID:29666258 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0003978 decreased circulating carnitine level IAGP N RGD:5509061 20230907 MGI PMID:35727412 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20230907 MGI PMID:35727412 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20230907 MGI PMID:35727412 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20180705 MGI PMID:29666258 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20230907 MGI PMID:35727412 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20230907 MGI PMID:35727412 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180705 MGI PMID:29666258 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0011230 abnormal folic acid level IAGP N RGD:5509061 20230907 MGI PMID:35727412 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0030658 increased glycine level IAGP N RGD:5509061 20230907 MGI PMID:35727412 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0030659 decreased glycine level IAGP N RGD:5509061 20230907 MGI PMID:35727412 1558601 Slc25a32 solute carrier family 25, member 32 gene MP:0030691 increased serine level IAGP N RGD:5509061 20230907 MGI PMID:35727412 1558602 Steap4 STEAP family member 4 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:17482547 1558602 Steap4 STEAP family member 4 gene MP:0030022 decreased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:17482547 1558603 Mcts1 malignant T cell amplified sequence 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1558603 Mcts1 malignant T cell amplified sequence 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210128 MGI 1558603 Mcts1 malignant T cell amplified sequence 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1558603 Mcts1 malignant T cell amplified sequence 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1558605 Sez6l2 seizure related 6 homolog like 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16814779 1558605 Sez6l2 seizure related 6 homolog like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16814779 1558605 Sez6l2 seizure related 6 homolog like 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16814779 1558605 Sez6l2 seizure related 6 homolog like 2 gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20141003 MGI PMID:16814779 1558605 Sez6l2 seizure related 6 homolog like 2 gene MP:0011268 biphasic excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:16814779 1558605 Sez6l2 seizure related 6 homolog like 2 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:16814779 1558605 Sez6l2 seizure related 6 homolog like 2 gene MP:0011272 short excitatory postsynaptic current rise time IAGP N RGD:5509061 20141003 MGI PMID:16814779 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0000071 axial skeleton hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10856223 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:10856223 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10856223 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:10856223 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10856223 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:10856223 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10856223 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0003359 hypaxial muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0005162 carpoptosis IAGP N RGD:5509061 20141003 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20160407 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16738228 1558606 Ptprd protein tyrosine phosphatase receptor type D gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12415267 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9671496 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:9671496 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9671496 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12415267 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12591907 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15238603 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19620960 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9671496 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12591907 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19620960 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9671496 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:15238603 1558608 Cbl Casitas B-lineage lymphoma gene MP:0001123 dilated uterus IAGP N RGD:5509061 20141003 MGI PMID:12591907 1558608 Cbl Casitas B-lineage lymphoma gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:12415267 1558608 Cbl Casitas B-lineage lymphoma gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12415267 1558608 Cbl Casitas B-lineage lymphoma gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12415267 1558608 Cbl Casitas B-lineage lymphoma gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:12415267 1558608 Cbl Casitas B-lineage lymphoma gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15238603 1558608 Cbl Casitas B-lineage lymphoma gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15238603 1558608 Cbl Casitas B-lineage lymphoma gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:15238603 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12591907 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12415267 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19620960 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15238603 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002364 abnormal thymus size IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:9671496 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12591907 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12591907 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20211021 MGI 1558608 Cbl Casitas B-lineage lymphoma gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15238603 1558608 Cbl Casitas B-lineage lymphoma gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12415267 1558608 Cbl Casitas B-lineage lymphoma gene MP:0003896 prolonged PR interval IEA N RGD:5509061 20211021 MGI 1558608 Cbl Casitas B-lineage lymphoma gene MP:0003948 abnormal gas homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19620960 1558608 Cbl Casitas B-lineage lymphoma gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12415267 1558608 Cbl Casitas B-lineage lymphoma gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:9671496 1558608 Cbl Casitas B-lineage lymphoma gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12415267 1558608 Cbl Casitas B-lineage lymphoma gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15238603 1558608 Cbl Casitas B-lineage lymphoma gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:12591907 1558608 Cbl Casitas B-lineage lymphoma gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:9671496 1558608 Cbl Casitas B-lineage lymphoma gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:9671496 1558608 Cbl Casitas B-lineage lymphoma gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:9671496 1558608 Cbl Casitas B-lineage lymphoma gene MP:0008904 abnormal mammary fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:9671496 1558608 Cbl Casitas B-lineage lymphoma gene MP:0009069 dilated oviduct IAGP N RGD:5509061 20141003 MGI PMID:12591907 1558608 Cbl Casitas B-lineage lymphoma gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0009379 abnormal foot pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17130487 1558608 Cbl Casitas B-lineage lymphoma gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20150402 MGI PMID:12591907 1558608 Cbl Casitas B-lineage lymphoma gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558608 Cbl Casitas B-lineage lymphoma gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16211006 1558608 Cbl Casitas B-lineage lymphoma gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:15520865 1558608 Cbl Casitas B-lineage lymphoma gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:15520865 1558609 Fezf1 Fez family zinc finger 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:16971467 1558609 Fezf1 Fez family zinc finger 1 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:16971467 1558609 Fezf1 Fez family zinc finger 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:16971467 1558609 Fezf1 Fez family zinc finger 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:19479999 1558609 Fezf1 Fez family zinc finger 1 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:19479999 1558609 Fezf1 Fez family zinc finger 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141120 MGI 1558609 Fezf1 Fez family zinc finger 1 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:16540508 1558609 Fezf1 Fez family zinc finger 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:16540508 1558609 Fezf1 Fez family zinc finger 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:16971467 1558609 Fezf1 Fez family zinc finger 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:19479999 1558609 Fezf1 Fez family zinc finger 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:19479999 1558609 Fezf1 Fez family zinc finger 1 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16540508 1558609 Fezf1 Fez family zinc finger 1 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:16540508 1558609 Fezf1 Fez family zinc finger 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:16540508 1558609 Fezf1 Fez family zinc finger 1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16540508 1558609 Fezf1 Fez family zinc finger 1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19479999 1558609 Fezf1 Fez family zinc finger 1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21452247 1558609 Fezf1 Fez family zinc finger 1 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:16971467 1558609 Fezf1 Fez family zinc finger 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16971467 1558609 Fezf1 Fez family zinc finger 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16540508 1558609 Fezf1 Fez family zinc finger 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19479999 1558609 Fezf1 Fez family zinc finger 1 gene MP:0011679 abnormal vomeronasal sensory neuron morphology IAGP N RGD:5509061 20150319 MGI PMID:21452247 1558609 Fezf1 Fez family zinc finger 1 gene MP:0013595 absent vomeronasal organ IAGP N RGD:5509061 20150319 MGI PMID:21452247 1558609 Fezf1 Fez family zinc finger 1 gene MP:0013597 small vomeronasal organ IAGP N RGD:5509061 20150319 MGI PMID:21452247 1558609 Fezf1 Fez family zinc finger 1 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:16971467 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20221006 MGI PMID:35151207 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20014010 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20014010 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22991445 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:22991445 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20014010 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22991445 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22991445 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:22991445 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:22991445 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:22991445 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:22991445 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22991445 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22991445 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22991445 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221006 MGI PMID:35151207 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221006 MGI PMID:35151207 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20221006 MGI PMID:35151207 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:22991445 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22991445 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221006 MGI PMID:35151207 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20014010 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14993285 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:14993285 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20221006 MGI PMID:35151207 1558610 Setdb1 SET domain, bifurcated 1 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:35151207 1558615 Slamf1 signaling lymphocytic activation molecule family member 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17135325 1558615 Slamf1 signaling lymphocytic activation molecule family member 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15123745 1558615 Slamf1 signaling lymphocytic activation molecule family member 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15123745 1558615 Slamf1 signaling lymphocytic activation molecule family member 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15123745 1558615 Slamf1 signaling lymphocytic activation molecule family member 1 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15539156 1558615 Slamf1 signaling lymphocytic activation molecule family member 1 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17202343 1558615 Slamf1 signaling lymphocytic activation molecule family member 1 gene MP:0020952 increased susceptibility to Paramyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:17135325 1558616 Glra4 glycine receptor, alpha 4 subunit gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20210128 MGI 1558618 Dcp2 decapping mRNA 2 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20201022 MGI PMID:32245620 1558618 Dcp2 decapping mRNA 2 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20201022 MGI PMID:32245620 1558618 Dcp2 decapping mRNA 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20201022 MGI PMID:32245620 1558618 Dcp2 decapping mRNA 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160421 MGI 1558618 Dcp2 decapping mRNA 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21070968 1558618 Dcp2 decapping mRNA 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20201022 MGI PMID:32245620 1558618 Dcp2 decapping mRNA 2 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20201022 MGI PMID:32245620 1558618 Dcp2 decapping mRNA 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20181227 MGI 1558618 Dcp2 decapping mRNA 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20201022 MGI PMID:32245620 1558618 Dcp2 decapping mRNA 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20201022 MGI PMID:32245620 1558618 Dcp2 decapping mRNA 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20201022 MGI PMID:32245620 1558618 Dcp2 decapping mRNA 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558618 Dcp2 decapping mRNA 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20201022 MGI PMID:32245620 1558619 Ctsb cathepsin B gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:12048238 1558619 Ctsb cathepsin B gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:17068745 1558619 Ctsb cathepsin B gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12782676 1558619 Ctsb cathepsin B gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12048238 1558619 Ctsb cathepsin B gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12048238 1558619 Ctsb cathepsin B gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:23054835 1558619 Ctsb cathepsin B gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23054835 1558619 Ctsb cathepsin B gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:12048238 1558619 Ctsb cathepsin B gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:20133781 1558619 Ctsb cathepsin B gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:12048238 1558619 Ctsb cathepsin B gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:23054835 1558619 Ctsb cathepsin B gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19664906 1558619 Ctsb cathepsin B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12048238 1558619 Ctsb cathepsin B gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:19664906 1558619 Ctsb cathepsin B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20133781 1558619 Ctsb cathepsin B gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:12048238 1558619 Ctsb cathepsin B gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12048238 1558619 Ctsb cathepsin B gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12048238 1558619 Ctsb cathepsin B gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:12048238 1558619 Ctsb cathepsin B gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20133781 1558619 Ctsb cathepsin B gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:20133781 1558619 Ctsb cathepsin B gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:19664906 1558619 Ctsb cathepsin B gene MP:0004155 decreased susceptibility to induced pancreatitis IAGP N RGD:5509061 20141003 MGI PMID:10995788 1558619 Ctsb cathepsin B gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12782676 1558619 Ctsb cathepsin B gene MP:0004697 abnormal thyroid follicular cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12782676 1558619 Ctsb cathepsin B gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:19664906 1558619 Ctsb cathepsin B gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:12782676 1558619 Ctsb cathepsin B gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15472011 1558619 Ctsb cathepsin B gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20133781 1558619 Ctsb cathepsin B gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:12048238 1558619 Ctsb cathepsin B gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:20133781 1558619 Ctsb cathepsin B gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20133781 1558619 Ctsb cathepsin B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12048238 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20221215 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000276 heart right ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000297 abnormal atrioventricular cushion morphology IEA N RGD:5509061 20111116 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20141003 MGI PMID:11912187 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:11912187 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000445 short snout IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000650 mesocardia IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11912187 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0001544 abnormal cardiovascular system physiology IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11912187 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:11912187 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0001872 sinus inflammation IAGP N RGD:5509061 20141003 MGI PMID:11912187 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:11912187 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20150813 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11912187 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:11912187 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11912187 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0002625 heart left ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0002639 micrognathia IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:11912187 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0003283 abnormal digestive organ placement IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0003446 renal hypoplasia IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0003675 kidney cyst IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0004017 duplex kidney IEA N RGD:5509061 20111116 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0004158 right aortic arch IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20230601 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20231207 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0006063 abnormal inferior vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:11912187 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0008461 left atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:11912187 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0009705 abnormal midgut morphology IEA N RGD:5509061 20150813 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0010405 ostium secundum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0010413 complete atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0010422 heart right ventricle hypoplasia IEA N RGD:5509061 20150326 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0010435 abnormal heart atrium and ventricle connection IEA N RGD:5509061 20111201 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0010440 anomalous pulmonary venous connection IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0010441 total anomalous pulmonary venous connection IEA N RGD:5509061 20150326 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0010460 pulmonary artery hypoplasia IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0010466 vascular ring IEA N RGD:5509061 20150226 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0010487 abnormal right subclavian artery morphology IEA N RGD:5509061 20150326 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0010808 right-sided stomach IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0010854 lung situs inversus IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011249 abdominal situs inversus IEA N RGD:5509061 20111201 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011250 abdominal situs ambiguus IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011252 situs inversus totalis IEA N RGD:5509061 20111116 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011253 situs inversus with levocardia IEA N RGD:5509061 20111201 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011254 superior-inferior ventricles IAGP N RGD:5509061 20141003 MGI PMID:18037990 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011510 biventricular, discordant atrioventricular connection IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011511 biventricular, ambiguous atrioventricular connection IEA N RGD:5509061 20111215 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011649 immotile respiratory cilia IAGP N RGD:5509061 20141003 MGI PMID:11912187 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20141003 MGI 1558622 Dnah5 dynein, axonemal, heavy chain 5 gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:11912187 1558623 Itgb1bp2 integrin beta 1 binding protein 2 gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:12496958 1558623 Itgb1bp2 integrin beta 1 binding protein 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12496958 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15073151 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170209 MGI 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15073151 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:15073151 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20170209 MGI 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0003051 curly tail IEA N RGD:5509061 20170209 MGI 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15073151 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20170105 MGI 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20170209 MGI 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0008816 petechiae IEA N RGD:5509061 20170209 MGI 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0010417 subarterial ventricular septal defect IEA N RGD:5509061 20170209 MGI 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0010460 pulmonary artery hypoplasia IEA N RGD:5509061 20170209 MGI 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0010586 absent conotruncal ridges IAGP N RGD:5509061 20141003 MGI PMID:15073151 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15073151 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558624 Bmp10 bone morphogenetic protein 10 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20160225 MGI PMID:23812757 1558625 Nkx6-3 NK6 homeobox 3 gene MP:0004137 abnormal gastric surface mucous cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18347062 1558625 Nkx6-3 NK6 homeobox 3 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18347062 1558625 Nkx6-3 NK6 homeobox 3 gene MP:0004732 decreased circulating gastrin level IAGP N RGD:5509061 20141003 MGI PMID:18347062 1558625 Nkx6-3 NK6 homeobox 3 gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20141003 MGI PMID:18347062 1558625 Nkx6-3 NK6 homeobox 3 gene MP:0010803 abnormal stomach enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18347062 1558626 Zfp536 zinc finger protein 536 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1558626 Zfp536 zinc finger protein 536 gene MP:0001575 cyanosis IEA N RGD:5509061 20210520 MGI 1558626 Zfp536 zinc finger protein 536 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20201022 MGI 1558626 Zfp536 zinc finger protein 536 gene MP:0005388 respiratory system phenotype IEA N RGD:5509061 20160811 MGI 1558626 Zfp536 zinc finger protein 536 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20190502 MGI 1558626 Zfp536 zinc finger protein 536 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160421 MGI 1558626 Zfp536 zinc finger protein 536 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1558713 Ethm3_m ethanol induced thermoregulation 3 (mouse) qtl MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20111116 MGI PMID:11773602 1558713 Ethm3_m ethanol induced thermoregulation 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11773602 1558717 Ses1a_m salmonella enteritidis susceptibility 1a (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12058254 1558718 Scpro9_m Stem cell proliferation 9 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:11698278 1558718 Scpro9_m Stem cell proliferation 9 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11698278 1558720 Bpq8_m blood pressure QTL 8 (mouse) qtl MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20111116 MGI PMID:14996992 1558720 Bpq8_m blood pressure QTL 8 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14996992 1558722 Htas3_m hypothermia due to alcohol sensitivity 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8169823 1558722 Htas3_m hypothermia due to alcohol sensitivity 3 (mouse) qtl MP:0005443 abnormal ethanol metabolism IAGP N RGD:5509061 20111116 MGI PMID:8169823 1558722 Htas3_m hypothermia due to alcohol sensitivity 3 (mouse) qtl MP:0005534 decreased body temperature IAGP N RGD:5509061 20111116 MGI PMID:8169823 1558724 Manln19_m mandible length 19 (mouse) qtl MP:0004593 long mandible IAGP N RGD:5509061 20111116 MGI PMID:15384169 1558724 Manln19_m mandible length 19 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1558724 Manln19_m mandible length 19 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1558728 Idd25_m insulin dependent diabetes susceptibility 25 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:16015371 1558728 Idd25_m insulin dependent diabetes susceptibility 25 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16015371 1558729 Vacq3_m voluntary alcohol consumption QTL 3 (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:16104380 1558729 Vacq3_m voluntary alcohol consumption QTL 3 (mouse) qtl MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:16104380 1558729 Vacq3_m voluntary alcohol consumption QTL 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16104380 1558732 Mfiq2_m M16 feed intake QTL 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15944354 1558732 Mfiq2_m M16 feed intake QTL 2 (mouse) qtl MP:0005449 abnormal food intake IAGP N RGD:5509061 20111116 MGI PMID:15944354 1558733 Mfeq1_m M16 feed efficiency QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15944354 1558733 Mfeq1_m M16 feed efficiency QTL 1 (mouse) qtl MP:0005449 abnormal food intake IAGP N RGD:5509061 20111116 MGI PMID:15944354 1558735 Egq2_m early growth QTL 2 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558735 Egq2_m early growth QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558736 Swrl2_m SWR lupus locus 2 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:11739537 1558736 Swrl2_m SWR lupus locus 2 (mouse) qtl MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:15693014 1558736 Swrl2_m SWR lupus locus 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15693014 1558736 Swrl2_m SWR lupus locus 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15693014 1558737 Vacq4_m voluntary alcohol consumption QTL 4 (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:16104380 1558737 Vacq4_m voluntary alcohol consumption QTL 4 (mouse) qtl MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:16104380 1558737 Vacq4_m voluntary alcohol consumption QTL 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16104380 1558738 W6q1_m weight 6 weeks QTL 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558738 W6q1_m weight 6 weeks QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558739 Lgaq2_m late growth adjusted QTL 2 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558739 Lgaq2_m late growth adjusted QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558740 Bpq9_m blood pressure QTL 9 (mouse) qtl MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20111116 MGI PMID:14996992 1558740 Bpq9_m blood pressure QTL 9 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14996992 1558741 Ses10_m salmonella enteritidis susceptibility 10 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:15973461 1558741 Ses10_m salmonella enteritidis susceptibility 10 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15973461 1558742 Ses4_m salmonella enteritidis susceptibility 4 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:15973461 1558742 Ses4_m salmonella enteritidis susceptibility 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15973461 1558743 Kcal1_m kilocalorie 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12388789 1558743 Kcal1_m kilocalorie 1 (mouse) qtl MP:0011939 increased food intake IAGP N RGD:5509061 20130328 MGI PMID:12388789 1558744 Salpa1_m serum alkaline phosphatase activity 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15542033 1558744 Salpa1_m serum alkaline phosphatase activity 1 (mouse) qtl MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20120209 MGI PMID:15542033 1558745 Tsiq1_m T-cell secretion of IL-4 QTL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15815685 1558745 Tsiq1_m T-cell secretion of IL-4 QTL 1 (mouse) qtl MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20111116 MGI PMID:15815685 1558746 lla_m lymphoma latency acceleration (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9209340 1558746 lla_m lymphoma latency acceleration (mouse) qtl MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20131227 MGI PMID:8641972 1558746 lla_m lymphoma latency acceleration (mouse) qtl MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20131227 MGI PMID:9209340 1558748 Vacq1_m voluntary alcohol consumption QTL 1 (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:16104380 1558748 Vacq1_m voluntary alcohol consumption QTL 1 (mouse) qtl MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:16104380 1558748 Vacq1_m voluntary alcohol consumption QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16104380 1558749 Psl3_m promotion susceptibility QTL 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12782578 1558749 Psl3_m promotion susceptibility QTL 3 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:12782578 1558749 Psl3_m promotion susceptibility QTL 3 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12782578 1558751 Bomd6_m bone mineral density 6 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:11697791 1558751 Bomd6_m bone mineral density 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11697791 1558752 Bntq1_m bone traits QTL 1 (mouse) qtl MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20111116 MGI PMID:15619674 1558752 Bntq1_m bone traits QTL 1 (mouse) qtl MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20111116 MGI PMID:15619674 1558752 Bntq1_m bone traits QTL 1 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15619674 1558752 Bntq1_m bone traits QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15619674 1558752 Bntq1_m bone traits QTL 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15619674 1558752 Bntq1_m bone traits QTL 1 (mouse) qtl MP:0008158 increased diameter of femur IAGP N RGD:5509061 20111116 MGI PMID:15619674 1558753 Ath19_m atherosclerosis 19 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:14592847 1558753 Ath19_m atherosclerosis 19 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14592847|PMID:17641228 1558753 Ath19_m atherosclerosis 19 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20151218 MGI Created by mouse qtl pipeline PMID:14592847 1558754 Nsila1_m novelty/stress induced locomotor activation 1 (mouse) qtl MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:15904718 1558754 Nsila1_m novelty/stress induced locomotor activation 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15904718 1558755 Skmw7_m skeletal muscle weight 7 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15687484 1558755 Skmw7_m skeletal muscle weight 7 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15687484 1558755 Skmw7_m skeletal muscle weight 7 (mouse) qtl MP:0009423 increased extensor digitorum longus weight IAGP N RGD:5509061 20111116 MGI PMID:15687484 1558756 Tgct1_m testicular germ cell tumor 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12566386 1558756 Tgct1_m testicular germ cell tumor 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12566386 1558756 Tgct1_m testicular germ cell tumor 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12566386 1558756 Tgct1_m testicular germ cell tumor 1 (mouse) qtl MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:12566386 1558757 Eae34_m experimental allergic encephalomyelitis susceptibility 34 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:15917267 1558757 Eae34_m experimental allergic encephalomyelitis susceptibility 34 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15917267 1558758 Kcal2_m kilocalorie 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12388789 1558758 Kcal2_m kilocalorie 2 (mouse) qtl MP:0011939 increased food intake IAGP N RGD:5509061 20130322 MGI PMID:16946080 1558758 Kcal2_m kilocalorie 2 (mouse) qtl MP:0011939 increased food intake IAGP N RGD:5509061 20130328 MGI PMID:12388789 1558759 Ap4q_m alcohol preference 4 QTL (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:9726281 1558759 Ap4q_m alcohol preference 4 QTL (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9726281 1558760 Nsila4_m novelty/stress induced locomotor activation 4 (mouse) qtl MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:15904718 1558760 Nsila4_m novelty/stress induced locomotor activation 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15904718 1558761 Nsila5_m novelty/stress induced locomotor activation 5 (mouse) qtl MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:15904718 1558761 Nsila5_m novelty/stress induced locomotor activation 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15904718 1558763 Gct9_m granulosa cell tumorigenesis 9 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15735010 1558763 Gct9_m granulosa cell tumorigenesis 9 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15735010 1558763 Gct9_m granulosa cell tumorigenesis 9 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15735010 1558763 Gct9_m granulosa cell tumorigenesis 9 (mouse) qtl MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20131227 MGI PMID:15735010 1558764 Scpro10_m Stem cell proliferation 10 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:11698278 1558764 Scpro10_m Stem cell proliferation 10 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11698278 1558765 Tesw1_m testis weight 1 (mouse) qtl MP:0004851 increased testis weight IAGP N RGD:5509061 20111116 MGI PMID:11333241 1558765 Tesw1_m testis weight 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11333241 1558765 Tesw1_m testis weight 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11333241 1558766 Mmtp2_m modifier of mammary tumor progression 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15859357 1558766 Mmtp2_m modifier of mammary tumor progression 2 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:15859357 1558767 Skmw11_m skeletal muscle weight 11 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15687484 1558767 Skmw11_m skeletal muscle weight 11 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15687484 1558767 Skmw11_m skeletal muscle weight 11 (mouse) qtl MP:0009423 increased extensor digitorum longus weight IAGP N RGD:5509061 20111116 MGI PMID:15687484 1558767 Skmw11_m skeletal muscle weight 11 (mouse) qtl MP:0009425 increased soleus weight IAGP N RGD:5509061 20111116 MGI PMID:15687484 1558767 Skmw11_m skeletal muscle weight 11 (mouse) qtl MP:0009427 increased tibialis anterior weight IAGP N RGD:5509061 20111116 MGI PMID:15687484 1558767 Skmw11_m skeletal muscle weight 11 (mouse) qtl MP:0009427 increased tibialis anterior weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 1558768 Mfi7q1_m M16 feed intake at 7 weeks QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15944354 1558768 Mfi7q1_m M16 feed intake at 7 weeks QTL 1 (mouse) qtl MP:0005449 abnormal food intake IAGP N RGD:5509061 20111116 MGI PMID:15944354 1558769 Zolw1_m zolpidem withdrawal 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16436183 1558769 Zolw1_m zolpidem withdrawal 1 (mouse) qtl MP:0009775 increased behavioral withdrawal response IAGP N RGD:5509061 20111116 MGI PMID:16436183 1558770 Mnif2_m macronutrient intake, fat 2 (mouse) qtl MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20111116 MGI PMID:12388789 1558770 Mnif2_m macronutrient intake, fat 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12388789 1558771 Eae35_m experimental allergic encephalomyelitis susceptibility 35 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:15917267 1558771 Eae35_m experimental allergic encephalomyelitis susceptibility 35 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15917267 1558772 Lith23_m lithogenic gene 23 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:15834632 1558772 Lith23_m lithogenic gene 23 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15834632 1558774 Lith17_m lithogenic gene 17 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:15834632 1558774 Lith17_m lithogenic gene 17 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151694|PMID:15834632 1558774 Lith17_m lithogenic gene 17 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20150724 MGI Created by mouse qtl pipeline PMID:15834632 1558775 Eclc_m epistatic circling C C57L/J 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11932245 1558776 Artmd1_m arthropathy in MRL and DBA/1 mice 1 (mouse) qtl MP:0002936 joint swelling IAGP N RGD:5509061 20111116 MGI PMID:15751084 1558776 Artmd1_m arthropathy in MRL and DBA/1 mice 1 (mouse) qtl MP:0003189 fused joints IAGP N RGD:5509061 20111116 MGI PMID:15751084 1558776 Artmd1_m arthropathy in MRL and DBA/1 mice 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15751084 1558776 Artmd1_m arthropathy in MRL and DBA/1 mice 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15751084 1558777 Marq2_m methamphetamine response QTL 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16104378 1558777 Marq2_m methamphetamine response QTL 2 (mouse) qtl MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20111116 MGI PMID:16104378 1558779 Eclb_m epistatic circling B C57L/J (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11932245 1558780 Idd22_m insulin dependent diabetes susceptibility 22 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:14513297 1558780 Idd22_m insulin dependent diabetes susceptibility 22 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14513297 1558782 Orgwq9_m organ weight QTL 9 (mouse) qtl MP:0002833 increased heart weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1558782 Orgwq9_m organ weight QTL 9 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1558782 Orgwq9_m organ weight QTL 9 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1558782 Orgwq9_m organ weight QTL 9 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12118102 1558782 Orgwq9_m organ weight QTL 9 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1558783 Idd26_m insulin dependent diabetes susceptibility 26 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:16015371 1558783 Idd26_m insulin dependent diabetes susceptibility 26 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16015371 1558785 Ablp_m absorbance of eye lens protein (mouse) qtl MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20111116 MGI PMID:15519297 1558785 Ablp_m absorbance of eye lens protein (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15519297 1558787 Cplaq8_m circadian period of locomotor activity 8 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15332441 1558787 Cplaq8_m circadian period of locomotor activity 8 (mouse) qtl MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:15332441 1558788 Ptnu2_m proteinuria 2 (mouse) qtl MP:0002962 increased urine protein level IAGP N RGD:5509061 20111116 MGI PMID:15965785 1558788 Ptnu2_m proteinuria 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15965785 1558788 Ptnu2_m proteinuria 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15965785 1558790 Mmtp1_m modifier of mammary tumor progression 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15859357 1558790 Mmtp1_m modifier of mammary tumor progression 1 (mouse) qtl MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20111116 MGI PMID:15859357 1558790 Mmtp1_m modifier of mammary tumor progression 1 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:15859357 1558791 Mlepq1_m M16 leptin QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15944354 1558791 Mlepq1_m M16 leptin QTL 1 (mouse) qtl MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20111116 MGI PMID:15944354 1558792 Htas4_m hypothermia due to alcohol sensitivity 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8169823 1558792 Htas4_m hypothermia due to alcohol sensitivity 4 (mouse) qtl MP:0005443 abnormal ethanol metabolism IAGP N RGD:5509061 20111116 MGI PMID:8169823 1558792 Htas4_m hypothermia due to alcohol sensitivity 4 (mouse) qtl MP:0005534 decreased body temperature IAGP N RGD:5509061 20111116 MGI PMID:8169823 1558793 Scc11_m colon tumor susceptibility 11 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14562056 1558793 Scc11_m colon tumor susceptibility 11 (mouse) qtl MP:0002020 increased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:14562056 1558794 Agnm1_m autoimmune glomerulonephritis in MRL 1 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:15832294 1558794 Agnm1_m autoimmune glomerulonephritis in MRL 1 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:15832294 1558794 Agnm1_m autoimmune glomerulonephritis in MRL 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15832294 1558794 Agnm1_m autoimmune glomerulonephritis in MRL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15832294 1558796 Gsi2_m glomerulsclerosis index 2 (mouse) qtl MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16093645 1558796 Gsi2_m glomerulsclerosis index 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16093645 1558797 Scpro8_m Stem cell proliferation 8 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:11698278 1558797 Scpro8_m Stem cell proliferation 8 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11698278 1558799 Nba4_m New Zealand Black autoimmunity 4 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:15693014 1558799 Nba4_m New Zealand Black autoimmunity 4 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:15693014 1558799 Nba4_m New Zealand Black autoimmunity 4 (mouse) qtl MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:15693014 1558799 Nba4_m New Zealand Black autoimmunity 4 (mouse) qtl MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20111116 MGI PMID:12215897 1558799 Nba4_m New Zealand Black autoimmunity 4 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15693014 1558799 Nba4_m New Zealand Black autoimmunity 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15693014 1558799 Nba4_m New Zealand Black autoimmunity 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15693014 1558799 Nba4_m New Zealand Black autoimmunity 4 (mouse) qtl MP:0008502 increased IgG3 level IAGP N RGD:5509061 20111116 MGI PMID:12215897 1558801 Tsiq2_m T-cell secretion of IL-4 QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15815685 1558801 Tsiq2_m T-cell secretion of IL-4 QTL 2 (mouse) qtl MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20111116 MGI PMID:15815685 1558802 Skmw6_m skeletal muscle weight 6 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15687484 1558802 Skmw6_m skeletal muscle weight 6 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15687484 1558802 Skmw6_m skeletal muscle weight 6 (mouse) qtl MP:0009425 increased soleus weight IAGP N RGD:5509061 20111116 MGI PMID:15687484 1558802 Skmw6_m skeletal muscle weight 6 (mouse) qtl MP:0009425 increased soleus weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 1558802 Skmw6_m skeletal muscle weight 6 (mouse) qtl MP:0009427 increased tibialis anterior weight IAGP N RGD:5509061 20111116 MGI PMID:15687484 1558802 Skmw6_m skeletal muscle weight 6 (mouse) qtl MP:0009427 increased tibialis anterior weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 1558803 W3q16_m weight 3 weeks QTL 16 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558803 W3q16_m weight 3 weeks QTL 16 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558805 Bodw3_m body weight 3 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16151693 1558805 Bodw3_m body weight 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151693 1558806 Vacq5_m voluntary alcohol consumption QTL 5 (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:16104380 1558806 Vacq5_m voluntary alcohol consumption QTL 5 (mouse) qtl MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:16104380 1558806 Vacq5_m voluntary alcohol consumption QTL 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16104380 1558807 Ceat1_m chronic experimental autoimmune thyroiditis 1 (mouse) qtl MP:0002876 abnormal thyroid gland physiology IAGP N RGD:5509061 20111116 MGI PMID:12086944 1558807 Ceat1_m chronic experimental autoimmune thyroiditis 1 (mouse) qtl MP:0004825 increased susceptibility to experimental autoimmune thyroiditis IAGP N RGD:5509061 20111116 MGI PMID:12086944 1558807 Ceat1_m chronic experimental autoimmune thyroiditis 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12086944 1558807 Ceat1_m chronic experimental autoimmune thyroiditis 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12086944 1558808 Kdw1_m kidney weight 1 (mouse) qtl MP:0003918 decreased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:16093645 1558808 Kdw1_m kidney weight 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16093645 1558809 Lith20_m lithogenic gene 20 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:15834632 1558809 Lith20_m lithogenic gene 20 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15834632 1558811 Scc13_m colon tumor susceptibility 13 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14562056 1558811 Scc13_m colon tumor susceptibility 13 (mouse) qtl MP:0002020 increased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:14562056 1558812 Rafar_m retinoic acid induced forelimb autopod reduction (mouse) qtl MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20111116 MGI PMID:15781699 1558812 Rafar_m retinoic acid induced forelimb autopod reduction (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15781699 1558813 Lmrq5_m Leishmania major resistance QTL 5 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:9175833 1558813 Lmrq5_m Leishmania major resistance QTL 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9175833 1558814 Ducm1_m dsRNA-induced UCM 1 (mouse) qtl MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20111116 MGI PMID:14625548 1558814 Ducm1_m dsRNA-induced UCM 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14625548 1558815 Gstml_m gestational survival modifier locus (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15649944 1558815 Gstml_m gestational survival modifier locus (mouse) qtl MP:0010769 abnormal survival IAGP N RGD:5509061 20111116 MGI PMID:15649944 1558816 Bomd5_m bone mineral density 5 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:11697791 1558816 Bomd5_m bone mineral density 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11697791 1558818 Asm1_m autoimmune sialadenitis in MRL mice 1 (mouse) qtl MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20111116 MGI PMID:10616009 1558818 Asm1_m autoimmune sialadenitis in MRL mice 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10616009 1558819 Ossc2_m osteosarcoma susceptibility 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11893245|PMID:16331598 1558819 Ossc2_m osteosarcoma susceptibility 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20150807 MGI Created by mouse qtl pipeline PMID:11893245 1558819 Ossc2_m osteosarcoma susceptibility 2 (mouse) qtl MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20111116 MGI PMID:11893245 1558820 Moo1_m modifier of Odc1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16086382|PMID:11944982 1558820 Moo1_m modifier of Odc1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20151023 MGI Created by mouse qtl pipeline PMID:11944982 1558820 Moo1_m modifier of Odc1 (mouse) qtl MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:11944982 1558820 Moo1_m modifier of Odc1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20160506 MGI Created by mouse qtl pipeline PMID:14693723 1558825 Aabpr_m aberrant activation of B cell proliferation (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14695357 1558825 Aabpr_m aberrant activation of B cell proliferation (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14695357 1558825 Aabpr_m aberrant activation of B cell proliferation (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14695357 1558826 Spnw4_m spleen weight 4 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:16151693 1558826 Spnw4_m spleen weight 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16151693 1558826 Spnw4_m spleen weight 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151693 1558826 Spnw4_m spleen weight 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151693 1558828 Mfiq1_m M16 feed intake QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15944354 1558828 Mfiq1_m M16 feed intake QTL 1 (mouse) qtl MP:0005449 abnormal food intake IAGP N RGD:5509061 20111116 MGI PMID:15944354 1558829 W3q2_m weight 3 weeks QTL 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558829 W3q2_m weight 3 weeks QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558830 Egaq2_m early growth adjusted QTL 2 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558830 Egaq2_m early growth adjusted QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558832 Lmrq2_m Leishmania major resistance QTL 2 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:9175833 1558832 Lmrq2_m Leishmania major resistance QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9175833 1558833 Erars2_m erosive arthritis susceptibility 2 (mouse) qtl MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20111116 MGI PMID:15683449 1558833 Erars2_m erosive arthritis susceptibility 2 (mouse) qtl MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20111116 MGI PMID:15683449 1558833 Erars2_m erosive arthritis susceptibility 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15683449 1558833 Erars2_m erosive arthritis susceptibility 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15683449 1558834 Swrl3_m SWR lupus locus 3 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:15693014 1558834 Swrl3_m SWR lupus locus 3 (mouse) qtl MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:11739537 1558834 Swrl3_m SWR lupus locus 3 (mouse) qtl MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20111116 MGI PMID:15693014 1558834 Swrl3_m SWR lupus locus 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15693014 1558835 Bdw1_m body weight 1 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16093645 1558835 Bdw1_m body weight 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16093645 1558836 Dice1b_m determination of interleukin 4 commitment 1b (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:15596523 1558836 Dice1b_m determination of interleukin 4 commitment 1b (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15596523 1558837 Marq1_m methamphetamine response QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16104378 1558837 Marq1_m methamphetamine response QTL 1 (mouse) qtl MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20111116 MGI PMID:16104378 1558838 Mfiq5_m M16 feed intake QTL 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15944354 1558838 Mfiq5_m M16 feed intake QTL 5 (mouse) qtl MP:0005449 abnormal food intake IAGP N RGD:5509061 20111116 MGI PMID:15944354 1558842 Tailq2_m tail length QTL 2 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558842 Tailq2_m tail length QTL 2 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558843 Ecla_m epistatic circling A C57L/J 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11932245 1558844 Lith15_m lithogenic gene 15 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:16151694 1558844 Lith15_m lithogenic gene 15 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151694 1558845 Alprf_m alcohol preference (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:10719795 1558845 Alprf_m alcohol preference (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10719795 1558846 Hfib2_m hepatic fibrogenesis 2 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15995705 1558846 Hfib2_m hepatic fibrogenesis 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:15995705 1558848 Marq5_m methamphetamine response QTL 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16104378 1558848 Marq5_m methamphetamine response QTL 5 (mouse) qtl MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20111116 MGI PMID:16104378 1558849 W3q15_m weight 3 weeks QTL 15 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558849 W3q15_m weight 3 weeks QTL 15 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558850 Sgp3_m serum gp70 production 3 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15634937 1558850 Sgp3_m serum gp70 production 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15634937 1558852 Gnf2_m growth and fatness 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15769905 1558852 Gnf2_m growth and fatness 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15769905 1558852 Gnf2_m growth and fatness 2 (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:15769905 1558853 Knyw3_m kidney weight 3 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:16151693 1558853 Knyw3_m kidney weight 3 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151693 1558853 Knyw3_m kidney weight 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16151693 1558855 Eae30_m experimental allergic encephalomyelitis susceptibility 30 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15917267 1558855 Eae30_m experimental allergic encephalomyelitis susceptibility 30 (mouse) qtl MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20111116 MGI PMID:15917267 1558856 Scc14_m colon tumor susceptibility 14 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14562056 1558856 Scc14_m colon tumor susceptibility 14 (mouse) qtl MP:0002020 increased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:14562056 1558858 Scpro7_m Stem cell proliferation 7 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:11698278 1558858 Scpro7_m Stem cell proliferation 7 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11698278 1558859 Vacq2_m voluntary alcohol consumption QTL 2 (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:16104380 1558859 Vacq2_m voluntary alcohol consumption QTL 2 (mouse) qtl MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:16104380 1558859 Vacq2_m voluntary alcohol consumption QTL 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16104380 1558860 W10q7_m weight 10 weeks QTL 7 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558860 W10q7_m weight 10 weeks QTL 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558862 Lmrq3_m Leishmania major resistance QTL 3 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:9175833 1558862 Lmrq3_m Leishmania major resistance QTL 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9175833 1558863 Scpro5_m Stem cell proliferation 5 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:11698278 1558863 Scpro5_m Stem cell proliferation 5 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:15788535 1558863 Scpro5_m Stem cell proliferation 5 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11698278 1558865 Lith21_m lithogenic gene 21 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:15834632 1558865 Lith21_m lithogenic gene 21 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15834632 1558866 Lmrq6_m Leishmania major resistance QTL 6 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:9175833 1558866 Lmrq6_m Leishmania major resistance QTL 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9175833 1558867 Gnf3_m growth and fatness 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15769905 1558867 Gnf3_m growth and fatness 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15769905 1558867 Gnf3_m growth and fatness 3 (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:15769905 1558868 Ses9_m salmonella enteritidis susceptibility 9 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:15973461 1558868 Ses9_m salmonella enteritidis susceptibility 9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15973461 1558869 Abfp5_m abdominal fat percentage 5 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:16151693 1558869 Abfp5_m abdominal fat percentage 5 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151693 1558870 Eae36_m experimental allergic encephalomyelitis susceptibility 36 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20111116 MGI PMID:15917267 1558870 Eae36_m experimental allergic encephalomyelitis susceptibility 36 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15917267 1558871 Mfiq3_m M16 feed intake QTL 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15944354 1558871 Mfiq3_m M16 feed intake QTL 3 (mouse) qtl MP:0005449 abnormal food intake IAGP N RGD:5509061 20111116 MGI PMID:15944354 1558872 Ibdq1_m inflammatory bowel disease QTL 1 (mouse) qtl MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20111116 MGI PMID:12891551 1558872 Ibdq1_m inflammatory bowel disease QTL 1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12891551 1558872 Ibdq1_m inflammatory bowel disease QTL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12891551 1558872 Ibdq1_m inflammatory bowel disease QTL 1 (mouse) qtl MP:0009482 ileum inflammation IAGP N RGD:5509061 20111116 MGI PMID:12891551 1558873 Hrtfm7_m heart failure modifier 7 (mouse) qtl MP:0002082 postnatal lethality IAGP N RGD:5509061 20111116 MGI PMID:16075368 1558873 Hrtfm7_m heart failure modifier 7 (mouse) qtl MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20111116 MGI PMID:16075368 1558873 Hrtfm7_m heart failure modifier 7 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16075368 1558873 Hrtfm7_m heart failure modifier 7 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16075368 1558873 Hrtfm7_m heart failure modifier 7 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16075368 1558875 Eae31_m experimental allergic encephalomyelitis susceptibility 31 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15917267 1558875 Eae31_m experimental allergic encephalomyelitis susceptibility 31 (mouse) qtl MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20111116 MGI PMID:15917267 1558876 W3q14_m weight 3 weeks QTL 14 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558876 W3q14_m weight 3 weeks QTL 14 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558877 W10q1_m weight 10 weeks QTL 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558877 W10q1_m weight 10 weeks QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558880 Scc12_m colon tumor susceptibility 12 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14562056 1558880 Scc12_m colon tumor susceptibility 12 (mouse) qtl MP:0002020 increased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:14562056 1558881 Ses7_m salmonella enteritidis susceptibility 7 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:15973461 1558881 Ses7_m salmonella enteritidis susceptibility 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15973461 1558882 Tsvw1_m testis and seminal vesicles weight 1 (mouse) qtl MP:0004851 increased testis weight IAGP N RGD:5509061 20111116 MGI PMID:11333241 1558882 Tsvw1_m testis and seminal vesicles weight 1 (mouse) qtl MP:0004909 increased seminal vesicle weight IAGP N RGD:5509061 20111116 MGI PMID:11333241 1558882 Tsvw1_m testis and seminal vesicles weight 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11333241 1558882 Tsvw1_m testis and seminal vesicles weight 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11333241 1558883 Abfp4_m abdominal fat percentage 4 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:16151693 1558883 Abfp4_m abdominal fat percentage 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151693 1558884 Nsila7_m novelty/stress induced locomotor activation 7 (mouse) qtl MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:15904718 1558884 Nsila7_m novelty/stress induced locomotor activation 7 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15904718 1558889 Mfiq4_m M16 feed intake QTL 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15944354 1558889 Mfiq4_m M16 feed intake QTL 4 (mouse) qtl MP:0005449 abnormal food intake IAGP N RGD:5509061 20111116 MGI PMID:15944354 1558890 Lith18_m lithogenic gene 18 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:15834632 1558890 Lith18_m lithogenic gene 18 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15834632 1558892 Ptnu1_m proteinuria 1 (mouse) qtl MP:0002962 increased urine protein level IAGP N RGD:5509061 20111116 MGI PMID:15965785 1558892 Ptnu1_m proteinuria 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15965785 1558892 Ptnu1_m proteinuria 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15965785 1558893 Spir1_m Streptococcus pneumoniae infection resistance 1 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:12925893 1558893 Spir1_m Streptococcus pneumoniae infection resistance 1 (mouse) qtl MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:12925893 1558893 Spir1_m Streptococcus pneumoniae infection resistance 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12925893 1558894 Tlag1_m T lymphoma attenuation gene 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:2552132 1558894 Tlag1_m T lymphoma attenuation gene 1 (mouse) qtl MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20111215 MGI PMID:11813303 1558894 Tlag1_m T lymphoma attenuation gene 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:2552132 1558894 Tlag1_m T lymphoma attenuation gene 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20241101 MGI Created by mouse qtl pipeline PMID:2552132 1558894 Tlag1_m T lymphoma attenuation gene 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20241101 MGI Created by mouse qtl pipeline PMID:2552132 1558895 Nsila6_m novelty/stress induced locomotor activation 6 (mouse) qtl MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:15904718 1558895 Nsila6_m novelty/stress induced locomotor activation 6 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15904718 1558896 Motp1_m modifier of Trp53 1 (mouse) qtl MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20111116 MGI PMID:15181534 1558896 Motp1_m modifier of Trp53 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15181534 1558896 Motp1_m modifier of Trp53 1 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15181534 1558896 Motp1_m modifier of Trp53 1 (mouse) qtl MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20111116 MGI PMID:15181534 1558897 Bodw1_m body weight 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16151693 1558897 Bodw1_m body weight 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151693 1558898 Hpi1_m hapatic PMN infiltration 1 (mouse) qtl MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:11053246 1558898 Hpi1_m hapatic PMN infiltration 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11053246 1558899 Egq1_m early growth QTL 1 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558899 Egq1_m early growth QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558901 Skmw8_m skeletal muscle weight 8 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15687484 1558901 Skmw8_m skeletal muscle weight 8 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15687484 1558901 Skmw8_m skeletal muscle weight 8 (mouse) qtl MP:0009423 increased extensor digitorum longus weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 1558901 Skmw8_m skeletal muscle weight 8 (mouse) qtl MP:0009427 increased tibialis anterior weight IAGP N RGD:5509061 20111116 MGI PMID:15687484 1558901 Skmw8_m skeletal muscle weight 8 (mouse) qtl MP:0009427 increased tibialis anterior weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 1558902 Mnek1a_m modifier of Nek1 (NIMA-related expressed kinase 1), kidney weight and hematocrit (mouse) qtl MP:0000208 decreased hematocrit IAGP N RGD:5509061 20111116 MGI PMID:10366444 1558902 Mnek1a_m modifier of Nek1 (NIMA-related expressed kinase 1), kidney weight and hematocrit (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:10366444 1558902 Mnek1a_m modifier of Nek1 (NIMA-related expressed kinase 1), kidney weight and hematocrit (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10366444 1558902 Mnek1a_m modifier of Nek1 (NIMA-related expressed kinase 1), kidney weight and hematocrit (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:10366444 1558902 Mnek1a_m modifier of Nek1 (NIMA-related expressed kinase 1), kidney weight and hematocrit (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10366444 1558903 Salpa2_m serum alkaline phosphatase activity 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15542033 1558903 Salpa2_m serum alkaline phosphatase activity 2 (mouse) qtl MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20120209 MGI PMID:15542033 1558904 Nsila9_m novelty/stress induced locomotor activation 9 (mouse) qtl MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:15904718 1558904 Nsila9_m novelty/stress induced locomotor activation 9 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15904718 1558905 Gct7_m granulosa cell tumorigenesis 7 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15735010 1558905 Gct7_m granulosa cell tumorigenesis 7 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15735010 1558905 Gct7_m granulosa cell tumorigenesis 7 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15735010 1558905 Gct7_m granulosa cell tumorigenesis 7 (mouse) qtl MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20131227 MGI PMID:15735010 1558907 Spnw1_m spleen weight 1 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:16151693 1558907 Spnw1_m spleen weight 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16151693 1558907 Spnw1_m spleen weight 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151693 1558907 Spnw1_m spleen weight 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151693 1558908 W10q12_m weight 10 weeks QTL 12 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558908 W10q12_m weight 10 weeks QTL 12 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558912 Marq4_m methamphetamine response QTL 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16104378 1558912 Marq4_m methamphetamine response QTL 4 (mouse) qtl MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20111116 MGI PMID:16104378 1558913 Afw7_m abdominal fat weight QTL 7 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11116089|PMID:9725853 1558914 Artmd2_m arthropathy in MRL and DBA/1 mice 2 (mouse) qtl MP:0002936 joint swelling IAGP N RGD:5509061 20111116 MGI PMID:15751084 1558914 Artmd2_m arthropathy in MRL and DBA/1 mice 2 (mouse) qtl MP:0003189 fused joints IAGP N RGD:5509061 20111116 MGI PMID:15751084 1558914 Artmd2_m arthropathy in MRL and DBA/1 mice 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15751084 1558914 Artmd2_m arthropathy in MRL and DBA/1 mice 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15751084 1558915 W3q1_m weight 3 weeks QTL 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558915 W3q1_m weight 3 weeks QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558916 Egq5_m early growth QTL 5 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558916 Egq5_m early growth QTL 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558917 Gct8_m granulosa cell tumorigenesis 8 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15735010 1558917 Gct8_m granulosa cell tumorigenesis 8 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15735010 1558917 Gct8_m granulosa cell tumorigenesis 8 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15735010 1558917 Gct8_m granulosa cell tumorigenesis 8 (mouse) qtl MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20131227 MGI PMID:15735010 1558918 Manln16_m mandible length 16 (mouse) qtl MP:0004593 long mandible IAGP N RGD:5509061 20111116 MGI PMID:15384169 1558918 Manln16_m mandible length 16 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1558918 Manln16_m mandible length 16 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15384169 1558920 Trglyd_m triglycerides (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:15524312 1558920 Trglyd_m triglycerides (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15524312 1558921 Ethm2_m ethanol induced thermoregulation 2 (mouse) qtl MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20111116 MGI PMID:11773602 1558921 Ethm2_m ethanol induced thermoregulation 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11773602 1558925 Hivan1_m HIV-associated nephropathy 1 (mouse) qtl MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20111116 MGI PMID:14983036 1558925 Hivan1_m HIV-associated nephropathy 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14983036 1558927 Mfi5q1_m M16 feed intake at 5 weeks QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15944354 1558927 Mfi5q1_m M16 feed intake at 5 weeks QTL 1 (mouse) qtl MP:0005449 abnormal food intake IAGP N RGD:5509061 20111116 MGI PMID:15944354 1558928 Mord2_m modifier of retinal degeneration 2 (mouse) qtl MP:0003455 decreased susceptibility to induced retina damage IAGP N RGD:5509061 20111116 MGI PMID:15947737 1558928 Mord2_m modifier of retinal degeneration 2 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15947737 1558929 Gsi1_m glomerulsclerosis index 1 (mouse) qtl MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16093645 1558929 Gsi1_m glomerulsclerosis index 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16093645 1558930 Knyw4_m kidney weight 4 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:16151693 1558930 Knyw4_m kidney weight 4 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151693 1558930 Knyw4_m kidney weight 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16151693 1558931 Scpro4_m Stem cell proliferation 4 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:11698278 1558931 Scpro4_m Stem cell proliferation 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11698278 1558933 Ses1b_m salmonella enteritidis susceptibility 1b (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:15973461 1558933 Ses1b_m salmonella enteritidis susceptibility 1b (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15973461 1558934 Cplaq12_m circadian period of locomotor activity 12 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14667146 1558934 Cplaq12_m circadian period of locomotor activity 12 (mouse) qtl MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:14667146 1558936 Eae38_m experimental allergic encephalomyelitis susceptibility 38 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20111116 MGI PMID:15917267 1558936 Eae38_m experimental allergic encephalomyelitis susceptibility 38 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15917267 1558938 Ethm1_m ethanol induced thermoregulation 1 (mouse) qtl MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20111116 MGI PMID:11773602 1558938 Ethm1_m ethanol induced thermoregulation 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11773602 1558939 Gnf1_m growth and fatness 1 (mouse) qtl MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:15769905 1558939 Gnf1_m growth and fatness 1 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:15769905 1558939 Gnf1_m growth and fatness 1 (mouse) qtl MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20111116 MGI PMID:15769905 1558939 Gnf1_m growth and fatness 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15769905 1558939 Gnf1_m growth and fatness 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15769905 1558939 Gnf1_m growth and fatness 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15769905 1558939 Gnf1_m growth and fatness 1 (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:15769905 1558940 Imebt1_m imprinting effect on body traits 1 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:15761081 1558940 Imebt1_m imprinting effect on body traits 1 (mouse) qtl MP:0003122 maternal imprinting IAGP N RGD:5509061 20111116 MGI PMID:15761081 1558940 Imebt1_m imprinting effect on body traits 1 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:15761081 1558940 Imebt1_m imprinting effect on body traits 1 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15761081 1558940 Imebt1_m imprinting effect on body traits 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15761081 1558940 Imebt1_m imprinting effect on body traits 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15761081 1558940 Imebt1_m imprinting effect on body traits 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15761081 1558940 Imebt1_m imprinting effect on body traits 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15761081 1558942 Lith16_m lithogenic gene 16 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:16151694 1558942 Lith16_m lithogenic gene 16 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151694 1558943 Scpro6_m Stem cell proliferation 6 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:11698278 1558943 Scpro6_m Stem cell proliferation 6 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:17220891 1558943 Scpro6_m Stem cell proliferation 6 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11698278 1558945 Orgwq8_m organ weight QTL 8 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1558945 Orgwq8_m organ weight QTL 8 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1558945 Orgwq8_m organ weight QTL 8 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:12118102 1558945 Orgwq8_m organ weight QTL 8 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1558945 Orgwq8_m organ weight QTL 8 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1558945 Orgwq8_m organ weight QTL 8 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:12118102 1558945 Orgwq8_m organ weight QTL 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1558945 Orgwq8_m organ weight QTL 8 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12118102 1558946 Scpro11_m Stem cell proliferation 11 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:11698278 1558946 Scpro11_m Stem cell proliferation 11 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11698278 1558947 Ptnu5_m proteinuria 5 (mouse) qtl MP:0002962 increased urine protein level IAGP N RGD:5509061 20111116 MGI PMID:15965785 1558947 Ptnu5_m proteinuria 5 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15965785 1558947 Ptnu5_m proteinuria 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15965785 1558948 Ath8_m atherosclerosis 8 (mouse) qtl MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20111116 MGI PMID:15530921 1558948 Ath8_m atherosclerosis 8 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:15530921 1558948 Ath8_m atherosclerosis 8 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17916774|PMID:15530921 1558948 Ath8_m atherosclerosis 8 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20151218 MGI Created by mouse qtl pipeline PMID:15530921 1558950 Nsila3_m novelty/stress induced locomotor activation 3 (mouse) qtl MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:15904718 1558950 Nsila3_m novelty/stress induced locomotor activation 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15904718 1558951 mdlk1_m modifier of Dlk1 (mouse) qtl MP:0003787 abnormal imprinting IAGP N RGD:5509061 20111116 MGI PMID:15859358 1558951 mdlk1_m modifier of Dlk1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15859358 1558951 mdlk1_m modifier of Dlk1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15859358 1558954 Hypism_m hyperinsulinemia (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:15514201 1558954 Hypism_m hyperinsulinemia (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15514201 1558956 Lith19_m lithogenic gene 19 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:15834632 1558956 Lith19_m lithogenic gene 19 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15834632 1558958 Tesw2_m testis weight 2 (mouse) qtl MP:0004851 increased testis weight IAGP N RGD:5509061 20111116 MGI PMID:11333241 1558958 Tesw2_m testis weight 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11333241 1558958 Tesw2_m testis weight 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11333241 1558959 Eamcd2_m experimental autoimmune myocarditis 2 (mouse) qtl MP:0001856 myocarditis IAGP N RGD:5509061 20111116 MGI PMID:15699148 1558959 Eamcd2_m experimental autoimmune myocarditis 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15699148 1558959 Eamcd2_m experimental autoimmune myocarditis 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15699148 1558960 Mfe5q1_m M16 feed efficiency at 5 weeks QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15944354 1558960 Mfe5q1_m M16 feed efficiency at 5 weeks QTL 1 (mouse) qtl MP:0005449 abnormal food intake IAGP N RGD:5509061 20111116 MGI PMID:15944354 1558961 Nidd1_m non-insulin-dependent diabetes mellitus 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:9703330 1558961 Nidd1_m non-insulin-dependent diabetes mellitus 1 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:9703330 1558961 Nidd1_m non-insulin-dependent diabetes mellitus 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9703330 1558961 Nidd1_m non-insulin-dependent diabetes mellitus 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9703330 1558962 Cms1_m resistance to Coccidioides immitis 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10338499 1558962 Cms1_m resistance to Coccidioides immitis 1 (mouse) qtl MP:0005398 decreased susceptibility to fungal infection IAGP N RGD:5509061 20111116 MGI PMID:10338499 1558965 Hcs3_m hepatocarcinogenesis susceptibility 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8417808 1558965 Hcs3_m hepatocarcinogenesis susceptibility 3 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:8417808 1558965 Hcs3_m hepatocarcinogenesis susceptibility 3 (mouse) qtl MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8417808 1558966 W10q9_m weight 10 weeks QTL 9 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558966 W10q9_m weight 10 weeks QTL 9 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558967 Scc15_m colon tumor susceptibility 15 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14562056 1558967 Scc15_m colon tumor susceptibility 15 (mouse) qtl MP:0002020 increased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:14562056 1558968 Tbdr1_m body temperature response to dietary restriction, QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14999024 1558968 Tbdr1_m body temperature response to dietary restriction, QTL 1 (mouse) qtl MP:0005534 decreased body temperature IAGP N RGD:5509061 20111116 MGI PMID:14999024 1558969 W6q11_m weight 6 weeks QTL 11 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558969 W6q11_m weight 6 weeks QTL 11 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558971 Imebt2_m imprinting effect on body traits 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15761081 1558971 Imebt2_m imprinting effect on body traits 2 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:15761081 1558971 Imebt2_m imprinting effect on body traits 2 (mouse) qtl MP:0003122 maternal imprinting IAGP N RGD:5509061 20111116 MGI PMID:15761081 1558971 Imebt2_m imprinting effect on body traits 2 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15761081 1558971 Imebt2_m imprinting effect on body traits 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15761081 1558971 Imebt2_m imprinting effect on body traits 2 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15761081 1558971 Imebt2_m imprinting effect on body traits 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15761081 1558971 Imebt2_m imprinting effect on body traits 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15761081 1558972 Erars1_m erosive arthritis susceptibility 1 (mouse) qtl MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20111116 MGI PMID:15683449 1558972 Erars1_m erosive arthritis susceptibility 1 (mouse) qtl MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:15683449 1558972 Erars1_m erosive arthritis susceptibility 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15683449 1558972 Erars1_m erosive arthritis susceptibility 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15683449 1558974 Vacq6_m voluntary alcohol consumption QTL 6 (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:16104380 1558974 Vacq6_m voluntary alcohol consumption QTL 6 (mouse) qtl MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:16104380 1558974 Vacq6_m voluntary alcohol consumption QTL 6 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16104380 1558975 Marq3_m methamphetamine response QTL 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16104378 1558975 Marq3_m methamphetamine response QTL 3 (mouse) qtl MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20111116 MGI PMID:16104378 1558976 Ptnu4_m proteinuria 4 (mouse) qtl MP:0002962 increased urine protein level IAGP N RGD:5509061 20111116 MGI PMID:15965785 1558976 Ptnu4_m proteinuria 4 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15965785 1558976 Ptnu4_m proteinuria 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15965785 1558977 Skmw10_m skeletal muscle weight 10 (mouse) qtl MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20111116 MGI PMID:15687484 1558977 Skmw10_m skeletal muscle weight 10 (mouse) qtl MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20111116 MGI PMID:16783642 1558977 Skmw10_m skeletal muscle weight 10 (mouse) qtl MP:0003397 increased muscle weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 1558977 Skmw10_m skeletal muscle weight 10 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15687484 1558977 Skmw10_m skeletal muscle weight 10 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15687484 1558977 Skmw10_m skeletal muscle weight 10 (mouse) qtl MP:0009421 increased gastrocnemius weight IAGP N RGD:5509061 20111116 MGI PMID:15687484 1558978 Cplaq10_m circadian period of locomotor activity 10 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14667146 1558978 Cplaq10_m circadian period of locomotor activity 10 (mouse) qtl MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:14667146 1558979 Ofact_m open field activity (mouse) qtl MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20111116 MGI PMID:11544198 1558979 Ofact_m open field activity (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11544198 1558980 Idd15_m insulin dependent diabetes susceptibility 15 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:7556956 1558980 Idd15_m insulin dependent diabetes susceptibility 15 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7556956 1558982 Eae37_m experimental allergic encephalomyelitis susceptibility 37 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20111116 MGI PMID:15917267 1558982 Eae37_m experimental allergic encephalomyelitis susceptibility 37 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15917267 1558984 Cplaq9_m circadian period of locomotor activity 9 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14667146 1558984 Cplaq9_m circadian period of locomotor activity 9 (mouse) qtl MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:14667146 1558985 Eae32_m experimental allergic encephalomyelitis susceptibility 32 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15917267 1558985 Eae32_m experimental allergic encephalomyelitis susceptibility 32 (mouse) qtl MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20111116 MGI PMID:15917267 1558987 Psl4_m promotion susceptibility QTL 4 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12782578 1558987 Psl4_m promotion susceptibility QTL 4 (mouse) qtl MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:12782578 1558987 Psl4_m promotion susceptibility QTL 4 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12782578 1558988 Bodw2_m body weight 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16151693 1558988 Bodw2_m body weight 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151693 1558989 Gnf4_m growth and fatness 4 (mouse) qtl MP:0003402 decreased liver weight IAGP N RGD:5509061 20111116 MGI PMID:15769905 1558989 Gnf4_m growth and fatness 4 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15769905 1558990 Skmw9_m skeletal muscle weight 9 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15687484 1558990 Skmw9_m skeletal muscle weight 9 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15687484 1558990 Skmw9_m skeletal muscle weight 9 (mouse) qtl MP:0009421 increased gastrocnemius weight IAGP N RGD:5509061 20111116 MGI PMID:15687484 1558990 Skmw9_m skeletal muscle weight 9 (mouse) qtl MP:0009421 increased gastrocnemius weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 1558991 Tailq4_m tail length QTL 4 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558991 Tailq4_m tail length QTL 4 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558992 Ses8_m salmonella enteritidis susceptibility 8 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:15973461 1558992 Ses8_m salmonella enteritidis susceptibility 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15973461 1558993 Tdmq1_m type 2 diabetes modifying QTL 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15820311 1558993 Tdmq1_m type 2 diabetes modifying QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15820311 1558993 Tdmq1_m type 2 diabetes modifying QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15820311 1558993 Tdmq1_m type 2 diabetes modifying QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15820311 1558993 Tdmq1_m type 2 diabetes modifying QTL 1 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:15820311 1558993 Tdmq1_m type 2 diabetes modifying QTL 1 (mouse) qtl MP:0009300 increased parametrial fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15820311 1558994 W6q2_m weight 6 weeks QTL 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558994 W6q2_m weight 6 weeks QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558995 Tsiq3_m T-cell secretion of IL-4 QTL 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15815685 1558995 Tsiq3_m T-cell secretion of IL-4 QTL 3 (mouse) qtl MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20111116 MGI PMID:15815685 1558996 Bomd7_m bone mineral density 7 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:11697791 1558996 Bomd7_m bone mineral density 7 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11697791 1558997 Lgq2_m late growth QTL 2 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 1558997 Lgq2_m late growth QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 1558998 Ses5_m salmonella enteritidis susceptibility 5 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:15973461 1558998 Ses5_m salmonella enteritidis susceptibility 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15973461 1558999 Ethm4_m ethanol induced thermoregulation 4 (mouse) qtl MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20111116 MGI PMID:11773602 1558999 Ethm4_m ethanol induced thermoregulation 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11773602 1559000 Ossc1_m osteosarcoma susceptibility 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11893245 1559000 Ossc1_m osteosarcoma susceptibility 1 (mouse) qtl MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20111116 MGI PMID:11893245 1559001 Eae33_m experimental allergic encephalomyelitis susceptibility 33 (mouse) qtl MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:15917267 1559001 Eae33_m experimental allergic encephalomyelitis susceptibility 33 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15917267 1559002 Lmrq4_m Leishmania major resistance QTL 4 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:9175833 1559002 Lmrq4_m Leishmania major resistance QTL 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9175833 1559004 Mglcq1_m M16 glucose QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15944354 1559004 Mglcq1_m M16 glucose QTL 1 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:15944354 1559006 Ses6_m salmonella enteritidis susceptibility 6 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:15973461 1559006 Ses6_m salmonella enteritidis susceptibility 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15973461 1559008 Lith22_m lithogenic gene 22 (mouse) qtl MP:0002830 gallstones IAGP N RGD:5509061 20111116 MGI PMID:15834632 1559008 Lith22_m lithogenic gene 22 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15834632 1559009 Vacq7_m voluntary alcohol consumption QTL 7 (mouse) qtl MP:0001987 alcohol preference IAGP N RGD:5509061 20111116 MGI PMID:16104380 1559009 Vacq7_m voluntary alcohol consumption QTL 7 (mouse) qtl MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:16104380 1559009 Vacq7_m voluntary alcohol consumption QTL 7 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16104380 1559010 Nsila8_m novelty/stress induced locomotor activation 8 (mouse) qtl MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:15904718 1559010 Nsila8_m novelty/stress induced locomotor activation 8 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15904718 1559012 Nsila10_m novelty/stress induced locomotor activation 10 (mouse) qtl MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:15904718 1559012 Nsila10_m novelty/stress induced locomotor activation 10 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15904718 1559013 Htas2_m hypothermia due to alcohol sensitivity 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8169823 1559013 Htas2_m hypothermia due to alcohol sensitivity 2 (mouse) qtl MP:0005443 abnormal ethanol metabolism IAGP N RGD:5509061 20111116 MGI PMID:8169823 1559013 Htas2_m hypothermia due to alcohol sensitivity 2 (mouse) qtl MP:0005534 decreased body temperature IAGP N RGD:5509061 20111116 MGI PMID:8169823 1559014 Agnm3_m autoimmune glomerulonephritis in MRL 3 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:15832294 1559014 Agnm3_m autoimmune glomerulonephritis in MRL 3 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:15832294 1559014 Agnm3_m autoimmune glomerulonephritis in MRL 3 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15832294 1559014 Agnm3_m autoimmune glomerulonephritis in MRL 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15832294 1559015 Bodw4_m body weight 4 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16151693 1559015 Bodw4_m body weight 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16151693 1559016 Drsi_m DCC-related Spp1 induction (mouse) qtl MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20111116 MGI PMID:15039225 1559016 Drsi_m DCC-related Spp1 induction (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15039225 1559016 Drsi_m DCC-related Spp1 induction (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15039225 1559016 Drsi_m DCC-related Spp1 induction (mouse) qtl MP:0005568 increased circulating total protein level IAGP N RGD:5509061 20111116 MGI PMID:15039225 1559017 Lmrq1_m Leishmania major resistance QTL 1 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:9175833 1559017 Lmrq1_m Leishmania major resistance QTL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9175833 1559018 Mord3_m modifier of retinal degeneration 3 (mouse) qtl MP:0003455 decreased susceptibility to induced retina damage IAGP N RGD:5509061 20111116 MGI PMID:15947737 1559018 Mord3_m modifier of retinal degeneration 3 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15947737 1559019 Mlepq2_m M16 leptin QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15944354 1559019 Mlepq2_m M16 leptin QTL 2 (mouse) qtl MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20111116 MGI PMID:15944354 1559020 Mmtp3_m modifier of mammary tumor progression 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15859357 1559020 Mmtp3_m modifier of mammary tumor progression 3 (mouse) qtl MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20111116 MGI PMID:15859357 1559021 Tlag2_m T lymphoma attenuation gene 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11813303 1559021 Tlag2_m T lymphoma attenuation gene 2 (mouse) qtl MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20111215 MGI PMID:11813303 1559021 Tlag2_m T lymphoma attenuation gene 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:11813303 1559021 Tlag2_m T lymphoma attenuation gene 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20241101 MGI Created by mouse qtl pipeline PMID:11813303 1559021 Tlag2_m T lymphoma attenuation gene 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20241101 MGI Created by mouse qtl pipeline PMID:11813303 1559023 Gbrln_m granular brain lesions (mouse) qtl MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20111116 MGI PMID:12828934 1559023 Gbrln_m granular brain lesions (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12828934 1559024 Zit1_m zinc induced tolerance 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16026622 1559024 Zit1_m zinc induced tolerance 1 (mouse) qtl MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20111116 MGI PMID:16026622 1559025 Agnm2_m autoimmune glomerulonephritis in MRL 2 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:15832294 1559025 Agnm2_m autoimmune glomerulonephritis in MRL 2 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:15832294 1559025 Agnm2_m autoimmune glomerulonephritis in MRL 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15832294 1559025 Agnm2_m autoimmune glomerulonephritis in MRL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15832294 1559026 Nsila2_m novelty/stress induced locomotor activation 2 (mouse) qtl MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20111116 MGI PMID:15904718 1559026 Nsila2_m novelty/stress induced locomotor activation 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15904718 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0000756 forelimb paralysis IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0001393 ataxia IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0001575 cyanosis IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0012216 decreased plasmalogen level IAGP N RGD:5509061 20150625 MGI PMID:25176044 1607093 Pex10 peroxisomal biogenesis factor 10 gene MP:0031494 abnormal prenatal movement IAGP N RGD:5509061 20230810 MGI PMID:25176044 1607095 Snord115 small nucleolar RNA, C/D Box 115 cluster gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20210617 MGI PMID:33016258 1607095 Snord115 small nucleolar RNA, C/D Box 115 cluster gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20210617 MGI PMID:33016258 1607095 Snord115 small nucleolar RNA, C/D Box 115 cluster gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20210617 MGI PMID:33016258 1607119 Dgat2l6 diacylglycerol O-acyltransferase 2-like 6 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1607119 Dgat2l6 diacylglycerol O-acyltransferase 2-like 6 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1607119 Dgat2l6 diacylglycerol O-acyltransferase 2-like 6 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20181227 MGI 1607119 Dgat2l6 diacylglycerol O-acyltransferase 2-like 6 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1607119 Dgat2l6 diacylglycerol O-acyltransferase 2-like 6 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1607119 Dgat2l6 diacylglycerol O-acyltransferase 2-like 6 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1607175 Eid2b EP300 interacting inhibitor of differentiation 2B gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20220811 MGI 1607175 Eid2b EP300 interacting inhibitor of differentiation 2B gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20230601 MGI 1607175 Eid2b EP300 interacting inhibitor of differentiation 2B gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1607175 Eid2b EP300 interacting inhibitor of differentiation 2B gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1607175 Eid2b EP300 interacting inhibitor of differentiation 2B gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1607175 Eid2b EP300 interacting inhibitor of differentiation 2B gene MP:0010052 increased grip strength IEA N RGD:5509061 20220519 MGI 1607175 Eid2b EP300 interacting inhibitor of differentiation 2B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1607175 Eid2b EP300 interacting inhibitor of differentiation 2B gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1607290 Misfadt mitochondrial sheath formation associated divergent transcript gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20220901 MGI PMID:31956907 1607350 Majin membrane anchored junction protein gene MP:0001147 small testis IAGP N RGD:5509061 20211021 MGI PMID:34326397 1607350 Majin membrane anchored junction protein gene MP:0004805 absent oocytes IAGP N RGD:5509061 20211021 MGI PMID:34326397 1607350 Majin membrane anchored junction protein gene MP:0005159 azoospermia IAGP N RGD:5509061 20211021 MGI PMID:34326397 1607350 Majin membrane anchored junction protein gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20211021 MGI PMID:34326397 1607447 3930402G23Rik RIKEN cDNA 3930402G23 gene gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20240509 MGI PMID:35917881 1607447 3930402G23Rik RIKEN cDNA 3930402G23 gene gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20240509 MGI PMID:35917881 1607447 3930402G23Rik RIKEN cDNA 3930402G23 gene gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20240509 MGI PMID:35917881 1607447 3930402G23Rik RIKEN cDNA 3930402G23 gene gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20240509 MGI PMID:35917881 1607447 3930402G23Rik RIKEN cDNA 3930402G23 gene gene MP:0031265 increased susceptibility to hepatic steatosis IAGP N RGD:5509061 20240509 MGI PMID:35917881 1607458 Foxd3os Forkhead box D3 opposite strand gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230126 MGI PMID:29420831 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:18039655 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18039655 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15831459 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18039655 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:15831459 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9159106 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18039655 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:18039655 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18039655 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18039655 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:18039655 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:18039655 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0010883 trachea stenosis IAGP N RGD:5509061 20150212 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18039655 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12588969 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9159106 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15831459 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0013753 tracheomalacia IAGP N RGD:5509061 20150416 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0030262 frontal bossing IAGP N RGD:5509061 20171026 MGI PMID:19696890 1607539 n-TUtca2 nuclear encoded tRNA selenocysteine 2 (anticodon TCA) gene MP:0030297 outer ear hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:19696890 1607556 Mir9-3 microRNA 9-3 gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0004081 abnormal globus pallidus morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0004172 abnormal subpallium development IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0008031 decreased Cajal-Retzius cell number IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0008440 abnormal subplate morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607556 Mir9-3 microRNA 9-3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0004081 abnormal globus pallidus morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0004172 abnormal subpallium development IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0008031 decreased Cajal-Retzius cell number IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0008440 abnormal subplate morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607557 Mir9-2 microRNA 9-2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21368052 1607562 Mir26a-2 microRNA 26a-2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607562 Mir26a-2 microRNA 26a-2 gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607562 Mir26a-2 microRNA 26a-2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607562 Mir26a-2 microRNA 26a-2 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607562 Mir26a-2 microRNA 26a-2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607562 Mir26a-2 microRNA 26a-2 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607562 Mir26a-2 microRNA 26a-2 gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607562 Mir26a-2 microRNA 26a-2 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607562 Mir26a-2 microRNA 26a-2 gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607562 Mir26a-2 microRNA 26a-2 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607563 Mir24-2 microRNA 24-2 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20210805 MGI PMID:34107258 1607563 Mir24-2 microRNA 24-2 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20210805 MGI PMID:34107258 1607564 Mir1a-2 microRNA 1a-2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17397913 1607564 Mir1a-2 microRNA 1a-2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:17397913 1607564 Mir1a-2 microRNA 1a-2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17397913 1607564 Mir1a-2 microRNA 1a-2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:17397913 1607564 Mir1a-2 microRNA 1a-2 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:17397913 1607564 Mir1a-2 microRNA 1a-2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17397913 1607564 Mir1a-2 microRNA 1a-2 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:17397913 1607564 Mir1a-2 microRNA 1a-2 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0004122 abnormal sinus arrhythmia IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:17397913 1607564 Mir1a-2 microRNA 1a-2 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17397913 1607564 Mir1a-2 microRNA 1a-2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17397913 1607564 Mir1a-2 microRNA 1a-2 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:17397913 1607564 Mir1a-2 microRNA 1a-2 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17397913 1607564 Mir1a-2 microRNA 1a-2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:17397913 1607564 Mir1a-2 microRNA 1a-2 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0010577 abnormal heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:17397913 1607564 Mir1a-2 microRNA 1a-2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607564 Mir1a-2 microRNA 1a-2 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17397913 1607564 Mir1a-2 microRNA 1a-2 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20141003 MGI PMID:24252873 1607565 Mir196a-2 microRNA 196a-2 gene MP:0000480 increased rib number IAGP N RGD:5509061 20161117 MGI PMID:26283362 1607565 Mir196a-2 microRNA 196a-2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20161117 MGI PMID:26283362 1607565 Mir196a-2 microRNA 196a-2 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20161117 MGI PMID:26283362 1607565 Mir196a-2 microRNA 196a-2 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20161117 MGI PMID:26283362 1607565 Mir196a-2 microRNA 196a-2 gene MP:0010113 abnormal sacrum morphology IAGP N RGD:5509061 20161117 MGI PMID:26283362 1607569 Mir133a-2 microRNA 133a-2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19015276 1607569 Mir133a-2 microRNA 133a-2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:19015276 1607570 Mir129-2 microRNA 129-2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1607570 Mir129-2 microRNA 129-2 gene MP:0002764 short tibia IEA N RGD:5509061 20230601 MGI 1607570 Mir129-2 microRNA 129-2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 1607570 Mir129-2 microRNA 129-2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1607570 Mir129-2 microRNA 129-2 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20230601 MGI 1607570 Mir129-2 microRNA 129-2 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20230601 MGI 1607570 Mir129-2 microRNA 129-2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230601 MGI 1607570 Mir129-2 microRNA 129-2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20230601 MGI 1607570 Mir129-2 microRNA 129-2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1607570 Mir129-2 microRNA 129-2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20240523 MGI 1607570 Mir129-2 microRNA 129-2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 1607570 Mir129-2 microRNA 129-2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230601 MGI 1607572 Mir124a-3 microRNA 124a-3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230427 MGI PMID:35868558 1607572 Mir124a-3 microRNA 124a-3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230427 MGI PMID:35868558 1607572 Mir124a-3 microRNA 124a-3 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20230427 MGI PMID:35868558 1607572 Mir124a-3 microRNA 124a-3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230427 MGI PMID:35868558 1607573 Mir124a-2 microRNA 124a-2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20230427 MGI PMID:35868558 1607573 Mir124a-2 microRNA 124a-2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230427 MGI PMID:35868558 1607573 Mir124a-2 microRNA 124a-2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230427 MGI PMID:35868558 1607573 Mir124a-2 microRNA 124a-2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20230427 MGI PMID:35868558 1607573 Mir124a-2 microRNA 124a-2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20230427 MGI PMID:35868558 1607573 Mir124a-2 microRNA 124a-2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230427 MGI PMID:35868558 1607598 Mir218-2 microRNA 218-2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20170824 MGI PMID:26680198 1607598 Mir218-2 microRNA 218-2 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20170824 MGI PMID:26680198 1607598 Mir218-2 microRNA 218-2 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20170824 MGI PMID:26680198 1607598 Mir218-2 microRNA 218-2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20170824 MGI PMID:26680198 1607598 Mir218-2 microRNA 218-2 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20170824 MGI PMID:26680198 1607598 Mir218-2 microRNA 218-2 gene MP:0001054 failure of neuromuscular synapse presynaptic differentiation IAGP N RGD:5509061 20170824 MGI PMID:26680198 1607598 Mir218-2 microRNA 218-2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20170824 MGI PMID:26680198 1607598 Mir218-2 microRNA 218-2 gene MP:0002690 akinesia IAGP N RGD:5509061 20170824 MGI PMID:26680198 1607598 Mir218-2 microRNA 218-2 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20170824 MGI PMID:26680198 1607598 Mir218-2 microRNA 218-2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20170824 MGI PMID:26680198 1607598 Mir218-2 microRNA 218-2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170824 MGI PMID:26680198 1607598 Mir218-2 microRNA 218-2 gene MP:0020336 abnormal motor neuron dendrite morphology IAGP N RGD:5509061 20170824 MGI PMID:26680198 1607601 Mir350 microRNA 350 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20231207 MGI 1607619 Mir7-1 microRNA 7-1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190523 MGI PMID:29887379 1607621 Mir375 microRNA 375 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607621 Mir375 microRNA 375 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607621 Mir375 microRNA 375 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607621 Mir375 microRNA 375 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607621 Mir375 microRNA 375 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607621 Mir375 microRNA 375 gene MP:0002710 increased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607621 Mir375 microRNA 375 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607621 Mir375 microRNA 375 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607621 Mir375 microRNA 375 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607621 Mir375 microRNA 375 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607621 Mir375 microRNA 375 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607621 Mir375 microRNA 375 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607621 Mir375 microRNA 375 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607621 Mir375 microRNA 375 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607621 Mir375 microRNA 375 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607621 Mir375 microRNA 375 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19289822 1607645 Mir200b microRNA 200b gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:23765281 1607645 Mir200b microRNA 200b gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23765281 1607645 Mir200b microRNA 200b gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:23765281 1607645 Mir200b microRNA 200b gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:23765281 1607645 Mir200b microRNA 200b gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:23765281 1607645 Mir200b microRNA 200b gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:23765281 1607645 Mir200b microRNA 200b gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:23765281 1607645 Mir200b microRNA 200b gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:23765281 1607645 Mir200b microRNA 200b gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20141003 MGI PMID:23765281 1607653 Mir125a microRNA 125a gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20160602 MGI PMID:25963922 1607653 Mir125a microRNA 125a gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20160602 MGI PMID:25963922 1607653 Mir125a microRNA 125a gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20160602 MGI PMID:25963922 1607653 Mir125a microRNA 125a gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20160602 MGI PMID:25963922 1607653 Mir125a microRNA 125a gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20160602 MGI PMID:25963922 1607664 Mir29a microRNA 29a gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20201001 MGI PMID:30827505 1607664 Mir29a microRNA 29a gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20201001 MGI PMID:30827505 1607668 Mir26a-1 microRNA 26a-1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607668 Mir26a-1 microRNA 26a-1 gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607668 Mir26a-1 microRNA 26a-1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607668 Mir26a-1 microRNA 26a-1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607668 Mir26a-1 microRNA 26a-1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607668 Mir26a-1 microRNA 26a-1 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607668 Mir26a-1 microRNA 26a-1 gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607668 Mir26a-1 microRNA 26a-1 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607668 Mir26a-1 microRNA 26a-1 gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607668 Mir26a-1 microRNA 26a-1 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20200416 MGI PMID:32092075 1607673 Mir217 microRNA 217 gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20191017 MGI PMID:31367007 1607673 Mir217 microRNA 217 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20191017 MGI PMID:31367007 1607673 Mir217 microRNA 217 gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20191017 MGI PMID:31367007 1607674 Mir216a microRNA 216a gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20191017 MGI PMID:31367007 1607674 Mir216a microRNA 216a gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20191017 MGI PMID:31367007 1607674 Mir216a microRNA 216a gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20191017 MGI PMID:31367007 1607676 Mir214 microRNA 214 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20190207 MGI PMID:22426211 1607676 Mir214 microRNA 214 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20190207 MGI PMID:22426211 1607676 Mir214 microRNA 214 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20190207 MGI PMID:22426211 1607676 Mir214 microRNA 214 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20190207 MGI PMID:22426211 1607676 Mir214 microRNA 214 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20190207 MGI PMID:22426211 1607676 Mir214 microRNA 214 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20190207 MGI PMID:22426211 1607680 Mir210 microRNA 210 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20201015 MGI PMID:32141129 1607680 Mir210 microRNA 210 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23960236 1607680 Mir210 microRNA 210 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:23960236 1607680 Mir210 microRNA 210 gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:23960236 1607680 Mir210 microRNA 210 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:23960236 1607680 Mir210 microRNA 210 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20201015 MGI PMID:32141129 1607682 Mir208a microRNA 208a gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17379774 1607682 Mir208a microRNA 208a gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:19726871 1607682 Mir208a microRNA 208a gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17379774 1607682 Mir208a microRNA 208a gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:17379774 1607682 Mir208a microRNA 208a gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17379774 1607682 Mir208a microRNA 208a gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17379774 1607682 Mir208a microRNA 208a gene MP:0010510 absent P wave IAGP N RGD:5509061 20141003 MGI PMID:19726871 1607682 Mir208a microRNA 208a gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:19726871 1607684 Mir205 microRNA 205 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:23974039 1607684 Mir205 microRNA 205 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:23974039 1607684 Mir205 microRNA 205 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:23974039 1607684 Mir205 microRNA 205 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:24116130 1607684 Mir205 microRNA 205 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:23974039 1607684 Mir205 microRNA 205 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24116130 1607684 Mir205 microRNA 205 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24116130 1607684 Mir205 microRNA 205 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:23974039 1607684 Mir205 microRNA 205 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:23974039 1607684 Mir205 microRNA 205 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:24116130 1607684 Mir205 microRNA 205 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20141003 MGI PMID:24116130 1607684 Mir205 microRNA 205 gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20190919 MGI PMID:30982661 1607684 Mir205 microRNA 205 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:23974039 1607684 Mir205 microRNA 205 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:22570807 1607684 Mir205 microRNA 205 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23974039 1607684 Mir205 microRNA 205 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24116130 1607685 Mir204 microRNA 204 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20220721 MGI PMID:32487559 1607685 Mir204 microRNA 204 gene MP:0002871 albuminuria IAGP N RGD:5509061 20220721 MGI PMID:32487559 1607685 Mir204 microRNA 204 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20220721 MGI PMID:32487559 1607685 Mir204 microRNA 204 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20220721 MGI PMID:32487559 1607685 Mir204 microRNA 204 gene MP:0011316 abnormal kidney interlobular artery morphology IAGP N RGD:5509061 20220721 MGI PMID:32487559 1607685 Mir204 microRNA 204 gene MP:0021052 abnormal renal arterial blood pressure regulation IAGP N RGD:5509061 20220721 MGI PMID:32487559 1607688 Spata22 spermatogenesis associated 22 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1607688 Spata22 spermatogenesis associated 22 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1607688 Spata22 spermatogenesis associated 22 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1607688 Spata22 spermatogenesis associated 22 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:22011390 1607688 Spata22 spermatogenesis associated 22 gene MP:0001127 small ovary IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0001127 small ovary IAGP N RGD:5509061 20201224 MGI PMID:32388826 1607688 Spata22 spermatogenesis associated 22 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:22011390 1607688 Spata22 spermatogenesis associated 22 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20181227 MGI 1607688 Spata22 spermatogenesis associated 22 gene MP:0001147 small testis IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20201224 MGI PMID:32388826 1607688 Spata22 spermatogenesis associated 22 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22011390 1607688 Spata22 spermatogenesis associated 22 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0001924 infertility IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22011390 1607688 Spata22 spermatogenesis associated 22 gene MP:0001925 male infertility IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0001925 male infertility IAGP N RGD:5509061 20201224 MGI PMID:32388826 1607688 Spata22 spermatogenesis associated 22 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:22011390 1607688 Spata22 spermatogenesis associated 22 gene MP:0001926 female infertility IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0001926 female infertility IAGP N RGD:5509061 20201224 MGI PMID:32388826 1607688 Spata22 spermatogenesis associated 22 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20181227 MGI 1607688 Spata22 spermatogenesis associated 22 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:22011390 1607688 Spata22 spermatogenesis associated 22 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20201224 MGI PMID:32388826 1607688 Spata22 spermatogenesis associated 22 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1607688 Spata22 spermatogenesis associated 22 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:22011390 1607688 Spata22 spermatogenesis associated 22 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22011390 1607688 Spata22 spermatogenesis associated 22 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20201224 MGI PMID:32388826 1607688 Spata22 spermatogenesis associated 22 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20181227 MGI 1607688 Spata22 spermatogenesis associated 22 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:22011390 1607688 Spata22 spermatogenesis associated 22 gene MP:0005159 azoospermia IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:22011390 1607688 Spata22 spermatogenesis associated 22 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22011390 1607688 Spata22 spermatogenesis associated 22 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:22011390 1607688 Spata22 spermatogenesis associated 22 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:22011390 1607688 Spata22 spermatogenesis associated 22 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20201224 MGI PMID:32388826 1607688 Spata22 spermatogenesis associated 22 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20201224 MGI PMID:32388826 1607688 Spata22 spermatogenesis associated 22 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1607688 Spata22 spermatogenesis associated 22 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:22011390 1607688 Spata22 spermatogenesis associated 22 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20190314 MGI PMID:28297563 1607688 Spata22 spermatogenesis associated 22 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20201224 MGI PMID:32388826 1607688 Spata22 spermatogenesis associated 22 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20201224 MGI PMID:32388826 1607697 Klhl3 kelch-like 3 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20180607 MGI PMID:28052936 1607697 Klhl3 kelch-like 3 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20200402 MGI PMID:30148674 1607697 Klhl3 kelch-like 3 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220811 MGI 1607697 Klhl3 kelch-like 3 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20170105 MGI 1607697 Klhl3 kelch-like 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1607697 Klhl3 kelch-like 3 gene MP:0003017 decreased circulating bicarbonate level IAGP N RGD:5509061 20200402 MGI PMID:30148674 1607697 Klhl3 kelch-like 3 gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20180607 MGI PMID:28052936 1607697 Klhl3 kelch-like 3 gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20200402 MGI PMID:30148674 1607697 Klhl3 kelch-like 3 gene MP:0003030 acidemia IAGP N RGD:5509061 20180607 MGI PMID:28052936 1607697 Klhl3 kelch-like 3 gene MP:0003030 acidemia IAGP N RGD:5509061 20200402 MGI PMID:30148674 1607697 Klhl3 kelch-like 3 gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20150827 MGI PMID:24821705 1607697 Klhl3 kelch-like 3 gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20180607 MGI PMID:28052936 1607697 Klhl3 kelch-like 3 gene MP:0004757 abnormal distal convoluted tubule morphology IAGP N RGD:5509061 20180607 MGI PMID:28052936 1607697 Klhl3 kelch-like 3 gene MP:0005583 decreased renin activity IAGP N RGD:5509061 20200402 MGI PMID:30148674 1607697 Klhl3 kelch-like 3 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20200402 MGI PMID:30148674 1607697 Klhl3 kelch-like 3 gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20180607 MGI PMID:28052936 1607697 Klhl3 kelch-like 3 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20200402 MGI PMID:30148674 1607697 Klhl3 kelch-like 3 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20200402 MGI PMID:30148674 1607697 Klhl3 kelch-like 3 gene MP:0012339 hyperkalemia IAGP N RGD:5509061 20150827 MGI PMID:24821705 1607697 Klhl3 kelch-like 3 gene MP:0012339 hyperkalemia IAGP N RGD:5509061 20200402 MGI PMID:30148674 1607697 Klhl3 kelch-like 3 gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20150827 MGI PMID:24821705 1607697 Klhl3 kelch-like 3 gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20200402 MGI PMID:30148674 1608040 Lexis1 lipid responsive LXR-induced inhibitor of cholesterol synthesis 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20171116 MGI PMID:27251289 1608040 Lexis1 lipid responsive LXR-induced inhibitor of cholesterol synthesis 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20171116 MGI PMID:27251289 1608088 5430431A17Rik RIKEN cDNA 5430431A17 gene gene MP:0000275 heart hyperplasia IAGP N RGD:5509061 20181206 MGI PMID:30177572 1608088 5430431A17Rik RIKEN cDNA 5430431A17 gene gene MP:0002083 premature death IAGP N RGD:5509061 20181206 MGI PMID:30177572 1608088 5430431A17Rik RIKEN cDNA 5430431A17 gene gene MP:0002833 increased heart weight IAGP N RGD:5509061 20181206 MGI PMID:30177572 1608088 5430431A17Rik RIKEN cDNA 5430431A17 gene gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20181206 MGI PMID:30177572 1608088 5430431A17Rik RIKEN cDNA 5430431A17 gene gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20181206 MGI PMID:30177572 1608088 5430431A17Rik RIKEN cDNA 5430431A17 gene gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20181206 MGI PMID:30177572 1608088 5430431A17Rik RIKEN cDNA 5430431A17 gene gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20181206 MGI PMID:30177572 1608088 5430431A17Rik RIKEN cDNA 5430431A17 gene gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20181206 MGI PMID:30177572 1608088 5430431A17Rik RIKEN cDNA 5430431A17 gene gene MP:0010580 decreased heart left ventricle size IAGP N RGD:5509061 20181206 MGI PMID:30177572 1608089 Krtap7-1 keratin associated protein 7-1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1608089 Krtap7-1 keratin associated protein 7-1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1608089 Krtap7-1 keratin associated protein 7-1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1608089 Krtap7-1 keratin associated protein 7-1 gene MP:0000692 small spleen IEA N RGD:5509061 20230119 MGI 1608089 Krtap7-1 keratin associated protein 7-1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1608089 Krtap7-1 keratin associated protein 7-1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1608089 Krtap7-1 keratin associated protein 7-1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20240523 MGI 1608089 Krtap7-1 keratin associated protein 7-1 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:23369715 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0000467 abnormal esophagus morphology IAGP N RGD:5509061 20141003 MGI PMID:24381249 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20161229 MGI PMID:25909911 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:24381249 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:23369715 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:24381249 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0001954 respiratory distress IAGP N RGD:5509061 20161229 MGI PMID:25909911 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:24381249 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:23369715 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0003159 abnormal esophageal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:24381249 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:23369715 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0003641 small lung IAGP N RGD:5509061 20161229 MGI PMID:25909911 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:24381249 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:24381249 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0010502 ventricle myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23369715 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20161229 MGI PMID:25909911 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24381249 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20161229 MGI PMID:25909911 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23369715 1608137 Fendrr Foxf1 adjacent non-coding developmental regulatory RNA gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23369715 1608160 Mir324 microRNA 324 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20221201 MGI PMID:34001919 1608161 Mir31 microRNA 31 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20190912 MGI PMID:29051494 1608161 Mir31 microRNA 31 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20190912 MGI PMID:29051494 1608161 Mir31 microRNA 31 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20190912 MGI PMID:29051494 1608161 Mir31 microRNA 31 gene MP:0001661 extended life span IAGP N RGD:5509061 20190912 MGI PMID:29051494 1608161 Mir31 microRNA 31 gene MP:0001881 abnormal mammary gland physiology IAGP N RGD:5509061 20190912 MGI PMID:29051494 1608161 Mir31 microRNA 31 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20190912 MGI PMID:29051494 1608161 Mir31 microRNA 31 gene MP:0004135 abnormal mammary gland embryonic development IAGP N RGD:5509061 20190912 MGI PMID:29051494 1608161 Mir31 microRNA 31 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20190912 MGI PMID:29051494 1608161 Mir31 microRNA 31 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20190912 MGI PMID:29051494 1608161 Mir31 microRNA 31 gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20190912 MGI PMID:29051494 1608161 Mir31 microRNA 31 gene MP:0013716 hypolactation IAGP N RGD:5509061 20190912 MGI PMID:29051494 1608161 Mir31 microRNA 31 gene MP:0013782 abnormal mammary duct terminal end bud morphology IAGP N RGD:5509061 20190912 MGI PMID:29051494 1608163 Mir10a microRNA 10a gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24204315 1608163 Mir10a microRNA 10a gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24204315 1608163 Mir10a microRNA 10a gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24204315 1608164 Mir100 microRNA 100 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200402 MGI PMID:31293973 1608164 Mir100 microRNA 100 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20230601 MGI 1608164 Mir100 microRNA 100 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200402 MGI PMID:31293973 1608164 Mir100 microRNA 100 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200402 MGI PMID:31293973 1608164 Mir100 microRNA 100 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20230601 MGI 1608164 Mir100 microRNA 100 gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20200402 MGI PMID:31293973 1608167 Mir378a microRNA 378a gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22949648 1608167 Mir378a microRNA 378a gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22949648 1608167 Mir378a microRNA 378a gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:22949648 1608167 Mir378a microRNA 378a gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22949648 1608167 Mir378a microRNA 378a gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22949648 1608167 Mir378a microRNA 378a gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22949648 1608167 Mir378a microRNA 378a gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:22949648 1608167 Mir378a microRNA 378a gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22949648 1608167 Mir378a microRNA 378a gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22949648 1608167 Mir378a microRNA 378a gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22949648 1608167 Mir378a microRNA 378a gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:22949648 1608170 Mir96 microRNA 96 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:19363478 1608170 Mir96 microRNA 96 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19363478 1608170 Mir96 microRNA 96 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:19363478 1608170 Mir96 microRNA 96 gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:19363478 1608170 Mir96 microRNA 96 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:19363478 1608170 Mir96 microRNA 96 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20180830 MGI 1608170 Mir96 microRNA 96 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19363478 1608170 Mir96 microRNA 96 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19363478 1608170 Mir96 microRNA 96 gene MP:0004408 decreased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:19363478 1608170 Mir96 microRNA 96 gene MP:0004416 absent cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:19363478 1608170 Mir96 microRNA 96 gene MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:19363478 1608170 Mir96 microRNA 96 gene MP:0004516 fused vestibular hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:19363478 1608170 Mir96 microRNA 96 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:19363478 1608170 Mir96 microRNA 96 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:19363478 1608170 Mir96 microRNA 96 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:19363478 1608173 Mir7b microRNA 7b gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190523 MGI PMID:29887379 1608180 Mir485 microRNA 485 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20231109 MGI PMID:36161914 1608180 Mir485 microRNA 485 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20231109 MGI PMID:36161914 1608180 Mir485 microRNA 485 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20231109 MGI PMID:36161914 1608180 Mir485 microRNA 485 gene MP:0009119 increased brown fat cell size IAGP N RGD:5509061 20231109 MGI PMID:36161914 1608180 Mir485 microRNA 485 gene MP:0009128 decreased brown fat cell number IAGP N RGD:5509061 20231109 MGI PMID:36161914 1608185 Mir451a microRNA 451a gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608185 Mir451a microRNA 451a gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608185 Mir451a microRNA 451a gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608185 Mir451a microRNA 451a gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20679397 1608185 Mir451a microRNA 451a gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608185 Mir451a microRNA 451a gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608185 Mir451a microRNA 451a gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608185 Mir451a microRNA 451a gene MP:0001586 abnormal erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20679397 1608185 Mir451a microRNA 451a gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608185 Mir451a microRNA 451a gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608185 Mir451a microRNA 451a gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608185 Mir451a microRNA 451a gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608185 Mir451a microRNA 451a gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608185 Mir451a microRNA 451a gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608185 Mir451a microRNA 451a gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608185 Mir451a microRNA 451a gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608185 Mir451a microRNA 451a gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20679397 1608185 Mir451a microRNA 451a gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608185 Mir451a microRNA 451a gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608185 Mir451a microRNA 451a gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608185 Mir451a microRNA 451a gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608185 Mir451a microRNA 451a gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608185 Mir451a microRNA 451a gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20679397 1608185 Mir451a microRNA 451a gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608185 Mir451a microRNA 451a gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608185 Mir451a microRNA 451a gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608185 Mir451a microRNA 451a gene MP:0011171 increased number of Heinz bodies IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608185 Mir451a microRNA 451a gene MP:0011241 abnormal fetal derived definitive erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20679397 1608185 Mir451a microRNA 451a gene MP:0011594 decreased catalase activity IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608186 Mir449a microRNA 449a gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20191003 MGI PMID:29162901 1608189 Mir429 microRNA 429 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:23765281 1608189 Mir429 microRNA 429 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23765281 1608189 Mir429 microRNA 429 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:23765281 1608189 Mir429 microRNA 429 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:23765281 1608189 Mir429 microRNA 429 gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:23765281 1608189 Mir429 microRNA 429 gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:23765281 1608189 Mir429 microRNA 429 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:23765281 1608189 Mir429 microRNA 429 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:23765281 1608189 Mir429 microRNA 429 gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20141003 MGI PMID:23765281 1608190 Mir425 microRNA 425 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20191128 MGI PMID:31383850 1608190 Mir425 microRNA 425 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20191128 MGI PMID:31383850 1608190 Mir425 microRNA 425 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20191128 MGI PMID:31383850 1608190 Mir425 microRNA 425 gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20191128 MGI PMID:31383850 1608196 Mir379 microRNA 379 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20240627 MGI PMID:33398021 1608196 Mir379 microRNA 379 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20240627 MGI PMID:33398021 1608206 Mir34a microRNA 34a gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20160922 MGI PMID:25348795 1608206 Mir34a microRNA 34a gene MP:0000745 tremors IAGP N RGD:5509061 20160922 MGI PMID:25348795 1608206 Mir34a microRNA 34a gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20210520 MGI PMID:33787491 1608206 Mir34a microRNA 34a gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210520 MGI PMID:33787491 1608206 Mir34a microRNA 34a gene MP:0001297 microphthalmia IAGP N RGD:5509061 20210520 MGI PMID:33787491 1608206 Mir34a microRNA 34a gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20210520 MGI PMID:33787491 1608206 Mir34a microRNA 34a gene MP:0001401 jumpy IAGP N RGD:5509061 20210520 MGI PMID:33787491 1608206 Mir34a microRNA 34a gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20210520 MGI PMID:33787491 1608206 Mir34a microRNA 34a gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160922 MGI PMID:25348795 1608206 Mir34a microRNA 34a gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20160922 MGI PMID:25348795 1608206 Mir34a microRNA 34a gene MP:0001505 hunched posture IAGP N RGD:5509061 20210520 MGI PMID:33787491 1608206 Mir34a microRNA 34a gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180329 MGI PMID:28923932 1608206 Mir34a microRNA 34a gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210520 MGI PMID:33787491 1608206 Mir34a microRNA 34a gene MP:0001866 nasal inflammation IAGP N RGD:5509061 20180329 MGI PMID:28923932 1608206 Mir34a microRNA 34a gene MP:0001925 male infertility IAGP N RGD:5509061 20180329 MGI PMID:28923932 1608206 Mir34a microRNA 34a gene MP:0001926 female infertility IAGP N RGD:5509061 20180329 MGI PMID:28923932 1608206 Mir34a microRNA 34a gene MP:0002083 premature death IAGP N RGD:5509061 20210520 MGI PMID:33787491 1608206 Mir34a microRNA 34a gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:22564414 1608206 Mir34a microRNA 34a gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1608206 Mir34a microRNA 34a gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20180329 MGI PMID:28923932 1608206 Mir34a microRNA 34a gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20160922 MGI PMID:25348795 1608206 Mir34a microRNA 34a gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20180329 MGI PMID:28923932 1608206 Mir34a microRNA 34a gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20160922 MGI PMID:25348795 1608206 Mir34a microRNA 34a gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20210520 MGI PMID:33787491 1608206 Mir34a microRNA 34a gene MP:0003700 abnormal oviduct transport IAGP N RGD:5509061 20180329 MGI PMID:28923932 1608206 Mir34a microRNA 34a gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20210520 MGI PMID:33787491 1608206 Mir34a microRNA 34a gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20150226 MGI PMID:24642471 1608206 Mir34a microRNA 34a gene MP:0004728 abnormal efferent ductules of testis morphology IAGP N RGD:5509061 20180329 MGI PMID:28923932 1608206 Mir34a microRNA 34a gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:22160706 1608206 Mir34a microRNA 34a gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:22564414 1608206 Mir34a microRNA 34a gene MP:0005014 increased B cell number IAGP N RGD:5509061 20160922 MGI PMID:25348795 1608206 Mir34a microRNA 34a gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20160922 MGI PMID:25348795 1608206 Mir34a microRNA 34a gene MP:0005576 decreased pulmonary ventilation IAGP N RGD:5509061 20160922 MGI PMID:25348795 1608206 Mir34a microRNA 34a gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:22564414 1608206 Mir34a microRNA 34a gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22020437 1608206 Mir34a microRNA 34a gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20160922 MGI PMID:25348795 1608206 Mir34a microRNA 34a gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180329 MGI PMID:28923932 1608206 Mir34a microRNA 34a gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20160922 MGI PMID:25348795 1608206 Mir34a microRNA 34a gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20180329 MGI PMID:28923932 1608206 Mir34a microRNA 34a gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160922 MGI PMID:25348795 1608206 Mir34a microRNA 34a gene MP:0011053 decreased respiratory motile cilia number IAGP N RGD:5509061 20180329 MGI PMID:28923932 1608206 Mir34a microRNA 34a gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180329 MGI PMID:28923932 1608206 Mir34a microRNA 34a gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210520 MGI PMID:33787491 1608206 Mir34a microRNA 34a gene MP:0011644 abnormal oviduct epithelium motile cilium morphology IAGP N RGD:5509061 20180329 MGI PMID:28923932 1608206 Mir34a microRNA 34a gene MP:0012018 abnormal oviduct physiology IAGP N RGD:5509061 20180329 MGI PMID:28923932 1608206 Mir34a microRNA 34a gene MP:0014200 abnormal respiratory epithelium physiology IAGP N RGD:5509061 20180329 MGI PMID:28923932 1608209 Mir338 microRNA 338 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20200423 MGI PMID:31281513 1608209 Mir338 microRNA 338 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20200423 MGI PMID:31281513 1608209 Mir338 microRNA 338 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20200423 MGI PMID:31281513 1608209 Mir338 microRNA 338 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20200423 MGI PMID:31281513 1608212 Mir326 microRNA 326 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20241017 MGI PMID:38909535 1608212 Mir326 microRNA 326 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20241017 MGI PMID:38909535 1608212 Mir326 microRNA 326 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20241017 MGI PMID:38909535 1608214 Mir320 microRNA 320 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1608215 Mir32 microRNA 32 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20240222 MGI PMID:37451670 1608215 Mir32 microRNA 32 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20240222 MGI PMID:37451670 1608215 Mir32 microRNA 32 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20240222 MGI PMID:37451670 1608215 Mir32 microRNA 32 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20240222 MGI PMID:37451670 1608215 Mir32 microRNA 32 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20240222 MGI PMID:37451670 1608215 Mir32 microRNA 32 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20240222 MGI PMID:37451670 1608215 Mir32 microRNA 32 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240222 MGI PMID:37451670 1608215 Mir32 microRNA 32 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20240222 MGI PMID:37451670 1608215 Mir32 microRNA 32 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20240222 MGI PMID:37451670 1608215 Mir32 microRNA 32 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20240222 MGI PMID:37451670 1608215 Mir32 microRNA 32 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20240222 MGI PMID:37451670 1608215 Mir32 microRNA 32 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240222 MGI PMID:37451670 1608215 Mir32 microRNA 32 gene MP:0031601 decreased endoplasmic reticulum stress IAGP N RGD:5509061 20240418 MGI PMID:37451670 1608218 Mir301 microRNA 301 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20170216 MGI PMID:27462406 1608218 Mir301 microRNA 301 gene MP:0002083 premature death IAGP N RGD:5509061 20170216 MGI PMID:27462406 1608218 Mir301 microRNA 301 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20170216 MGI PMID:27462406 1608218 Mir301 microRNA 301 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20170216 MGI PMID:27462406 1608218 Mir301 microRNA 301 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20170216 MGI PMID:27462406 1608218 Mir301 microRNA 301 gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20170216 MGI PMID:27462406 1608218 Mir301 microRNA 301 gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20170216 MGI PMID:27462406 1608218 Mir301 microRNA 301 gene MP:0010285 decreased skin tumor incidence IAGP N RGD:5509061 20170216 MGI PMID:27462406 1608229 Mir218-1 microRNA 218-1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20170824 MGI PMID:26680198 1608229 Mir218-1 microRNA 218-1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20170824 MGI PMID:26680198 1608229 Mir218-1 microRNA 218-1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20170824 MGI PMID:26680198 1608229 Mir218-1 microRNA 218-1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20170824 MGI PMID:26680198 1608229 Mir218-1 microRNA 218-1 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20170824 MGI PMID:26680198 1608229 Mir218-1 microRNA 218-1 gene MP:0001054 failure of neuromuscular synapse presynaptic differentiation IAGP N RGD:5509061 20170824 MGI PMID:26680198 1608229 Mir218-1 microRNA 218-1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20170824 MGI PMID:26680198 1608229 Mir218-1 microRNA 218-1 gene MP:0002690 akinesia IAGP N RGD:5509061 20170824 MGI PMID:26680198 1608229 Mir218-1 microRNA 218-1 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20170824 MGI PMID:26680198 1608229 Mir218-1 microRNA 218-1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20170824 MGI PMID:26680198 1608229 Mir218-1 microRNA 218-1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170824 MGI PMID:26680198 1608229 Mir218-1 microRNA 218-1 gene MP:0020336 abnormal motor neuron dendrite morphology IAGP N RGD:5509061 20170824 MGI PMID:26680198 1608230 Mir199a-2 microRNA 199a-2 gene MP:0000745 tremors IAGP N RGD:5509061 20190912 MGI PMID:26344767 1608230 Mir199a-2 microRNA 199a-2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20190912 MGI PMID:26344767 1608230 Mir199a-2 microRNA 199a-2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190912 MGI PMID:26344767 1608230 Mir199a-2 microRNA 199a-2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190912 MGI PMID:26344767 1608230 Mir199a-2 microRNA 199a-2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190912 MGI PMID:26344767 1608230 Mir199a-2 microRNA 199a-2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20190912 MGI PMID:26344767 1608230 Mir199a-2 microRNA 199a-2 gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20190912 MGI PMID:26344767 1608230 Mir199a-2 microRNA 199a-2 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20190912 MGI PMID:26344767 1608230 Mir199a-2 microRNA 199a-2 gene MP:0002083 premature death IAGP N RGD:5509061 20190912 MGI PMID:26344767 1608230 Mir199a-2 microRNA 199a-2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20190912 MGI PMID:26344767 1608230 Mir199a-2 microRNA 199a-2 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20190912 MGI PMID:26344767 1608230 Mir199a-2 microRNA 199a-2 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20190912 MGI PMID:26344767 1608231 Mir196b microRNA 196b gene MP:0000480 increased rib number IAGP N RGD:5509061 20161117 MGI PMID:26283362 1608231 Mir196b microRNA 196b gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20161117 MGI PMID:26283362 1608231 Mir196b microRNA 196b gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20161117 MGI PMID:26283362 1608231 Mir196b microRNA 196b gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20161117 MGI PMID:26283362 1608231 Mir196b microRNA 196b gene MP:0010113 abnormal sacrum morphology IAGP N RGD:5509061 20161117 MGI PMID:26283362 1608234 Mir133b microRNA 133b gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22875923 1608236 Mir128-2 microRNA 128-2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:24311694 1608236 Mir128-2 microRNA 128-2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:24311694 1608236 Mir128-2 microRNA 128-2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24311694 1608236 Mir128-2 microRNA 128-2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24311694 1608236 Mir128-2 microRNA 128-2 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:24311694 1608236 Mir128-2 microRNA 128-2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:24311694 1608236 Mir128-2 microRNA 128-2 gene MP:0021019 increased dendritic spine number IAGP N RGD:5509061 20211014 MGI PMID:24311694 1608237 Mir223 microRNA 223 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18278031 1608237 Mir223 microRNA 223 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18278031 1608237 Mir223 microRNA 223 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18278031 1608237 Mir223 microRNA 223 gene MP:0002415 abnormal neutrophil differentiation IAGP N RGD:5509061 20141003 MGI PMID:18278031 1608237 Mir223 microRNA 223 gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18278031 1608237 Mir223 microRNA 223 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:18278031 1608237 Mir223 microRNA 223 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:18278031 1608292 Mir203 microRNA 203 gene MP:0001200 thick skin IAGP N RGD:5509061 20151224 MGI PMID:26203562 1608292 Mir203 microRNA 203 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151217 MGI PMID:26203562 1608292 Mir203 microRNA 203 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20151224 MGI PMID:26203562 1608292 Mir203 microRNA 203 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20151224 MGI PMID:26203562 1608293 Mir202 microRNA 202 gene MP:0001147 small testis IAGP N RGD:5509061 20230817 MGI PMID:35712867 1608293 Mir202 microRNA 202 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20230817 MGI PMID:35712867 1608293 Mir202 microRNA 202 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20230817 MGI PMID:35712867 1608293 Mir202 microRNA 202 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20230817 MGI PMID:35712867 1608293 Mir202 microRNA 202 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20230817 MGI PMID:35712867 1608293 Mir202 microRNA 202 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230817 MGI PMID:35712867 1608293 Mir202 microRNA 202 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20230817 MGI PMID:35712867 1608293 Mir202 microRNA 202 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20230817 MGI PMID:35712867 1608293 Mir202 microRNA 202 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20230817 MGI PMID:35712867 1608293 Mir202 microRNA 202 gene MP:0008967 absent chiasmata formation IAGP N RGD:5509061 20230817 MGI PMID:35712867 1608293 Mir202 microRNA 202 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20230817 MGI PMID:35712867 1608293 Mir202 microRNA 202 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20230817 MGI PMID:35712867 1608293 Mir202 microRNA 202 gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20230817 MGI PMID:35712867 1608293 Mir202 microRNA 202 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20230817 MGI PMID:35712867 1608293 Mir202 microRNA 202 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20230817 MGI PMID:35712867 1608300 Mir196a-1 microRNA 196a-1 gene MP:0000480 increased rib number IAGP N RGD:5509061 20161117 MGI PMID:26283362 1608300 Mir196a-1 microRNA 196a-1 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20161117 MGI PMID:26283362 1608300 Mir196a-1 microRNA 196a-1 gene MP:0004672 short ribs IAGP N RGD:5509061 20161117 MGI PMID:26283362 1608300 Mir196a-1 microRNA 196a-1 gene MP:0010113 abnormal sacrum morphology IAGP N RGD:5509061 20161117 MGI PMID:26283362 1608301 Mir195a microRNA 195a gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:33029941 1608304 Mir192 microRNA 192 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:23649518 1608304 Mir192 microRNA 192 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:23649518 1608304 Mir192 microRNA 192 gene MP:0006315 abnormal urine protein level IAGP N RGD:5509061 20141003 MGI PMID:23649518 1608304 Mir192 microRNA 192 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23649518 1608304 Mir192 microRNA 192 gene MP:0011338 abnormal mesangial matrix morphology IAGP N RGD:5509061 20141003 MGI PMID:23649518 1608308 Mir188 microRNA 188 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20160505 MGI PMID:25751060 1608308 Mir188 microRNA 188 gene MP:0004149 increased bone strength IAGP N RGD:5509061 20160505 MGI PMID:25751060 1608308 Mir188 microRNA 188 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20160505 MGI PMID:25751060 1608308 Mir188 microRNA 188 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20160505 MGI PMID:25751060 1608308 Mir188 microRNA 188 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20160505 MGI PMID:25751060 1608308 Mir188 microRNA 188 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20160505 MGI PMID:25751060 1608308 Mir188 microRNA 188 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20160505 MGI PMID:25751060 1608308 Mir188 microRNA 188 gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20160505 MGI PMID:25751060 1608308 Mir188 microRNA 188 gene MP:0013621 decreased internal diameter of femur IAGP N RGD:5509061 20160505 MGI PMID:25751060 1608308 Mir188 microRNA 188 gene MP:0013623 increased femur compact bone thickness IAGP N RGD:5509061 20160505 MGI PMID:25751060 1608308 Mir188 microRNA 188 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20160505 MGI PMID:25751060 1608308 Mir188 microRNA 188 gene MP:0013640 increased bone stiffness IAGP N RGD:5509061 20160505 MGI PMID:25751060 1608308 Mir188 microRNA 188 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:25751060 1608311 Mir185 microRNA 185 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20191024 MGI PMID:30787286 1608311 Mir185 microRNA 185 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20191024 MGI PMID:30787286 1608311 Mir185 microRNA 185 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20191024 MGI PMID:30787286 1608311 Mir185 microRNA 185 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20191024 MGI PMID:30787286 1608311 Mir185 microRNA 185 gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20191024 MGI PMID:30787286 1608311 Mir185 microRNA 185 gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20191024 MGI PMID:30787286 1608311 Mir185 microRNA 185 gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20191024 MGI PMID:30787286 1608311 Mir185 microRNA 185 gene MP:0012072 decreased susceptibility to osteoporosis IAGP N RGD:5509061 20191024 MGI PMID:30787286 1608311 Mir185 microRNA 185 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20191024 MGI PMID:30787286 1608311 Mir185 microRNA 185 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20191024 MGI PMID:30787286 1608311 Mir185 microRNA 185 gene MP:0030438 increased osteoblast proliferation IAGP N RGD:5509061 20191024 MGI PMID:30787286 1608312 Mir184 microRNA 184 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141009 MGI PMID:24361012 1608312 Mir184 microRNA 184 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141009 MGI PMID:24361012 1608312 Mir184 microRNA 184 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141009 MGI PMID:24361012 1608312 Mir184 microRNA 184 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141009 MGI PMID:24361012 1608312 Mir184 microRNA 184 gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20141009 MGI PMID:24361012 1608312 Mir184 microRNA 184 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20141009 MGI PMID:24361012 1608313 Mir183 microRNA 183 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20210506 MGI PMID:32176259 1608313 Mir183 microRNA 183 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20210506 MGI PMID:32176259 1608314 Mir182 microRNA 182 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20160204 MGI PMID:25180607 1608314 Mir182 microRNA 182 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160204 MGI PMID:25180607 1608318 Mir155 microRNA 155 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:17463290 1608318 Mir155 microRNA 155 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:17463290 1608318 Mir155 microRNA 155 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:17463290 1608318 Mir155 microRNA 155 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17463290 1608318 Mir155 microRNA 155 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150305 MGI PMID:25367574 1608318 Mir155 microRNA 155 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:17463290 1608318 Mir155 microRNA 155 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17463290 1608318 Mir155 microRNA 155 gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17463290 1608318 Mir155 microRNA 155 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17463290 1608318 Mir155 microRNA 155 gene MP:0002433 abnormal T-helper 1 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17463290 1608318 Mir155 microRNA 155 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20160218 MGI PMID:26163372 1608318 Mir155 microRNA 155 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17463290 1608318 Mir155 microRNA 155 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17463290 1608318 Mir155 microRNA 155 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20160218 MGI PMID:26163372 1608318 Mir155 microRNA 155 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:17463290 1608318 Mir155 microRNA 155 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:18455451 1608318 Mir155 microRNA 155 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19234151 1608318 Mir155 microRNA 155 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20160218 MGI PMID:26163372 1608318 Mir155 microRNA 155 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17463290 1608318 Mir155 microRNA 155 gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:17463290 1608318 Mir155 microRNA 155 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:17463290 1608318 Mir155 microRNA 155 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:17463289 1608318 Mir155 microRNA 155 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20160218 MGI PMID:26163372 1608318 Mir155 microRNA 155 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:18455451 1608318 Mir155 microRNA 155 gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20160218 MGI PMID:26163372 1608318 Mir155 microRNA 155 gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20160218 MGI PMID:26163372 1608318 Mir155 microRNA 155 gene MP:0013771 decreased effector memory T-helper cell number IAGP N RGD:5509061 20160218 MGI PMID:26163372 1608323 Mir150 microRNA 150 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:17923094 1608323 Mir150 microRNA 150 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:17923094 1608323 Mir150 microRNA 150 gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:17923094 1608323 Mir150 microRNA 150 gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:17923094 1608323 Mir150 microRNA 150 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:17923094 1608323 Mir150 microRNA 150 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:17923094 1608324 Mir149 microRNA 149 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20201001 MGI PMID:29029439 1608324 Mir149 microRNA 149 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20201001 MGI PMID:29029439 1608324 Mir149 microRNA 149 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20201001 MGI PMID:29029439 1608324 Mir149 microRNA 149 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20201001 MGI PMID:29029439 1608325 Mir148a microRNA 148a gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20210826 MGI PMID:33336366 1608325 Mir148a microRNA 148a gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20210826 MGI PMID:33336366 1608325 Mir148a microRNA 148a gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20210826 MGI PMID:33336366 1608325 Mir148a microRNA 148a gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20210826 MGI PMID:33336366 1608325 Mir148a microRNA 148a gene MP:0003926 decreased cellular glucose uptake IAGP N RGD:5509061 20210826 MGI PMID:33336366 1608325 Mir148a microRNA 148a gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20210826 MGI PMID:33336366 1608325 Mir148a microRNA 148a gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20210826 MGI PMID:33336366 1608325 Mir148a microRNA 148a gene MP:0008728 increased memory B cell number IAGP N RGD:5509061 20210826 MGI PMID:33336366 1608325 Mir148a microRNA 148a gene MP:0013940 abnormal plasmablast number IAGP N RGD:5509061 20210826 MGI PMID:33336366 1608325 Mir148a microRNA 148a gene MP:0020154 impaired humoral immune response IAGP N RGD:5509061 20210826 MGI PMID:33336366 1608327 Mir146 microRNA 146 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20171102 MGI PMID:26458771 1608327 Mir146 microRNA 146 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:20850013 1608327 Mir146 microRNA 146 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:20850013 1608327 Mir146 microRNA 146 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20850013 1608327 Mir146 microRNA 146 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20190926 MGI PMID:30013024 1608327 Mir146 microRNA 146 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:20850013 1608327 Mir146 microRNA 146 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20850013 1608327 Mir146 microRNA 146 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20190926 MGI PMID:30013024 1608327 Mir146 microRNA 146 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20171102 MGI PMID:26458771 1608327 Mir146 microRNA 146 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20850013 1608327 Mir146 microRNA 146 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:20850013 1608327 Mir146 microRNA 146 gene MP:0005000 abnormal immune tolerance IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20171102 MGI PMID:26458771 1608327 Mir146 microRNA 146 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:20850013 1608327 Mir146 microRNA 146 gene MP:0005649 increased spleen neoplasm incidence IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20190926 MGI PMID:30013024 1608327 Mir146 microRNA 146 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20190926 MGI PMID:30013024 1608327 Mir146 microRNA 146 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20190926 MGI PMID:30013024 1608327 Mir146 microRNA 146 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20850013 1608327 Mir146 microRNA 146 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0009317 increased follicular lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0009317 increased follicular lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0009439 increased myeloid sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20190926 MGI PMID:30013024 1608327 Mir146 microRNA 146 gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20850013 1608327 Mir146 microRNA 146 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608327 Mir146 microRNA 146 gene MP:0011076 increased macrophage nitric oxide production IAGP N RGD:5509061 20141003 MGI PMID:21555486 1608327 Mir146 microRNA 146 gene MP:0011747 myelofibrosis IAGP N RGD:5509061 20141003 MGI PMID:21576471 1608328 Mir145a microRNA 145a gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:19720868 1608328 Mir145a microRNA 145a gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19720868 1608328 Mir145a microRNA 145a gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19720868 1608328 Mir145a microRNA 145a gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:19720868 1608328 Mir145a microRNA 145a gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19720868 1608328 Mir145a microRNA 145a gene MP:0002976 vascular smooth muscle hypotrophy IAGP N RGD:5509061 20141003 MGI PMID:19720868 1608328 Mir145a microRNA 145a gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19720868 1608328 Mir145a microRNA 145a gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:19720868 1608328 Mir145a microRNA 145a gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19720868 1608328 Mir145a microRNA 145a gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19720868 1608328 Mir145a microRNA 145a gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19720868 1608328 Mir145a microRNA 145a gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19720868 1608329 Mir144 microRNA 144 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608329 Mir144 microRNA 144 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608329 Mir144 microRNA 144 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608329 Mir144 microRNA 144 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608329 Mir144 microRNA 144 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608329 Mir144 microRNA 144 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608329 Mir144 microRNA 144 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608329 Mir144 microRNA 144 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608329 Mir144 microRNA 144 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608329 Mir144 microRNA 144 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608329 Mir144 microRNA 144 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608329 Mir144 microRNA 144 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608329 Mir144 microRNA 144 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608329 Mir144 microRNA 144 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608329 Mir144 microRNA 144 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608329 Mir144 microRNA 144 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608329 Mir144 microRNA 144 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608329 Mir144 microRNA 144 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608329 Mir144 microRNA 144 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608329 Mir144 microRNA 144 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:20513743 1608329 Mir144 microRNA 144 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608329 Mir144 microRNA 144 gene MP:0011171 increased number of Heinz bodies IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608329 Mir144 microRNA 144 gene MP:0011594 decreased catalase activity IAGP N RGD:5509061 20141003 MGI PMID:20679398 1608330 Mir143 microRNA 143 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:19720868 1608330 Mir143 microRNA 143 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1608332 Mir140 microRNA 140 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20200604 MGI PMID:30804514 1608332 Mir140 microRNA 140 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:20466812 1608332 Mir140 microRNA 140 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20200604 MGI PMID:30804514 1608332 Mir140 microRNA 140 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:20466812 1608332 Mir140 microRNA 140 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:20466812 1608332 Mir140 microRNA 140 gene MP:0000445 short snout IAGP N RGD:5509061 20200604 MGI PMID:30804514 1608332 Mir140 microRNA 140 gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:20466812 1608332 Mir140 microRNA 140 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20466812 1608332 Mir140 microRNA 140 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21576357 1608332 Mir140 microRNA 140 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21576357 1608332 Mir140 microRNA 140 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200604 MGI PMID:30804514 1608332 Mir140 microRNA 140 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:20466812 1608332 Mir140 microRNA 140 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20466812 1608332 Mir140 microRNA 140 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21576357 1608332 Mir140 microRNA 140 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:21576357 1608332 Mir140 microRNA 140 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:21576357 1608332 Mir140 microRNA 140 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21576357 1608332 Mir140 microRNA 140 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20200604 MGI PMID:30804514 1608332 Mir140 microRNA 140 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:21576357 1608332 Mir140 microRNA 140 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:21576357 1608332 Mir140 microRNA 140 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:20466812 1608332 Mir140 microRNA 140 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20466812 1608332 Mir140 microRNA 140 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:21576357 1608332 Mir140 microRNA 140 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:20466812 1608332 Mir140 microRNA 140 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20200604 MGI PMID:30804514 1608332 Mir140 microRNA 140 gene MP:0004670 small vertebral body IAGP N RGD:5509061 20200604 MGI PMID:30804514 1608332 Mir140 microRNA 140 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:20466812 1608332 Mir140 microRNA 140 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:21576357 1608332 Mir140 microRNA 140 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:20466812 1608332 Mir140 microRNA 140 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21576357 1608332 Mir140 microRNA 140 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20200604 MGI PMID:30804514 1608332 Mir140 microRNA 140 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:20466812 1608332 Mir140 microRNA 140 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:21576357 1608332 Mir140 microRNA 140 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:21576357 1608332 Mir140 microRNA 140 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20190926 MGI PMID:29695789 1608332 Mir140 microRNA 140 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20466812 1608332 Mir140 microRNA 140 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:21576357 1608332 Mir140 microRNA 140 gene MP:0011175 platyspondylia IAGP N RGD:5509061 20200604 MGI PMID:30804514 1608332 Mir140 microRNA 140 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20200604 MGI PMID:30804514 1608333 Mir139 microRNA 139 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20191128 MGI PMID:27022656 1608333 Mir139 microRNA 139 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20201119 MGI PMID:26859226 1608333 Mir139 microRNA 139 gene MP:0005036 diarrhea IAGP N RGD:5509061 20191128 MGI PMID:27022656 1608333 Mir139 microRNA 139 gene MP:0005036 diarrhea IAGP N RGD:5509061 20201119 MGI PMID:26859226 1608333 Mir139 microRNA 139 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20201119 MGI PMID:26859226 1608333 Mir139 microRNA 139 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20201119 MGI PMID:26859226 1608333 Mir139 microRNA 139 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20191128 MGI PMID:27022656 1608333 Mir139 microRNA 139 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20201119 MGI PMID:26859226 1608333 Mir139 microRNA 139 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20191128 MGI PMID:27022656 1608333 Mir139 microRNA 139 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20191128 MGI PMID:27022656 1608333 Mir139 microRNA 139 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20201119 MGI PMID:26859226 1608333 Mir139 microRNA 139 gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20191128 MGI PMID:27022656 1608333 Mir139 microRNA 139 gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20201119 MGI PMID:26859226 1608333 Mir139 microRNA 139 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20201119 MGI PMID:26859226 1608333 Mir139 microRNA 139 gene MP:0014234 decreased enterocyte apoptosis IAGP N RGD:5509061 20230323 MGI PMID:27022656 1608335 Mir137 microRNA 137 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180315 MGI PMID:25016316 1608342 Mir128-1 microRNA 128-1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24311694 1608343 Mir127 microRNA 127 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20160915 MGI PMID:26138477 1608343 Mir127 microRNA 127 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160915 MGI PMID:26138477 1608343 Mir127 microRNA 127 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20160915 MGI PMID:26138477 1608343 Mir127 microRNA 127 gene MP:0004265 abnormal placental transport IAGP N RGD:5509061 20160915 MGI PMID:26138477 1608343 Mir127 microRNA 127 gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20160915 MGI PMID:26138477 1608343 Mir127 microRNA 127 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20160915 MGI PMID:26138477 1608343 Mir127 microRNA 127 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20160915 MGI PMID:26138477 1608343 Mir127 microRNA 127 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20160915 MGI PMID:26138477 1608343 Mir127 microRNA 127 gene MP:0011526 abnormal placenta fetal blood space morphology IAGP N RGD:5509061 20160915 MGI PMID:26138477 1608345 Mir10b microRNA 10b gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20231221 MGI PMID:37723933 1608345 Mir10b microRNA 10b gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20231221 MGI PMID:37723933 1608345 Mir10b microRNA 10b gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20231221 MGI PMID:37723933 1608345 Mir10b microRNA 10b gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20231221 MGI PMID:37723933 1608345 Mir10b microRNA 10b gene MP:0005331 insulin resistance IAGP N RGD:5509061 20231221 MGI PMID:37723933 1608345 Mir10b microRNA 10b gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20231221 MGI PMID:37723933 1608345 Mir10b microRNA 10b gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20231221 MGI PMID:37723933 1608345 Mir10b microRNA 10b gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20231221 MGI PMID:37723933 1608345 Mir10b microRNA 10b gene MP:0009854 impaired gastric peristalsis IAGP N RGD:5509061 20231221 MGI PMID:37723933 1608345 Mir10b microRNA 10b gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20231221 MGI PMID:37723933 1608347 Mir24-1 microRNA 24-1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20210805 MGI PMID:34107258 1608347 Mir24-1 microRNA 24-1 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20210805 MGI PMID:34107258 1608348 Mir22 microRNA 22 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190207 MGI PMID:28314781 1608348 Mir22 microRNA 22 gene MP:0001544 abnormal cardiovascular system physiology IEA N RGD:5509061 20141003 MGI 1608348 Mir22 microRNA 22 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141016 MGI PMID:23524588 1608348 Mir22 microRNA 22 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20190207 MGI PMID:28314781 1608348 Mir22 microRNA 22 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20190207 MGI PMID:28314781 1608348 Mir22 microRNA 22 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141016 MGI PMID:23524588 1608348 Mir22 microRNA 22 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141016 MGI PMID:23524588 1608348 Mir22 microRNA 22 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141016 MGI PMID:23524588 1608348 Mir22 microRNA 22 gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20141003 MGI 1608348 Mir22 microRNA 22 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20190207 MGI PMID:28314781 1608348 Mir22 microRNA 22 gene MP:0006138 congestive heart failure IEA N RGD:5509061 20141003 MGI 1608348 Mir22 microRNA 22 gene MP:0008022 dilated heart ventricle IEA N RGD:5509061 20141003 MGI 1608348 Mir22 microRNA 22 gene MP:0008873 increased physiological sensitivity to xenobiotic IEA N RGD:5509061 20141003 MGI 1608348 Mir22 microRNA 22 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20190207 MGI PMID:28314781 1608348 Mir22 microRNA 22 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20190207 MGI PMID:28314781 1608348 Mir22 microRNA 22 gene MP:0020135 abnormal heart ventricle wall thickness IAGP N RGD:5509061 20141016 MGI PMID:23524588 1608349 Mir21a microRNA 21a gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:23527070 1608349 Mir21a microRNA 21a gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832755 1608349 Mir21a microRNA 21a gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20832755 1608349 Mir21a microRNA 21a gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20832755 1608349 Mir21a microRNA 21a gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:20978354 1608349 Mir21a microRNA 21a gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:21849676 1608349 Mir21a microRNA 21a gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20832755 1608349 Mir21a microRNA 21a gene MP:0003907 decreased aorta elastin content IAGP N RGD:5509061 20141003 MGI PMID:23527070 1608349 Mir21a microRNA 21a gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:22344686 1608349 Mir21a microRNA 21a gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:21646541 1608349 Mir21a microRNA 21a gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23527070 1608349 Mir21a microRNA 21a gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:21646541 1608349 Mir21a microRNA 21a gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:23527070 1608349 Mir21a microRNA 21a gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:21849676 1608349 Mir21a microRNA 21a gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:21849676 1608349 Mir21a microRNA 21a gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23527070 1608349 Mir21a microRNA 21a gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:21849676 1608349 Mir21a microRNA 21a gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:21849676 1608349 Mir21a microRNA 21a gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:21849676 1608349 Mir21a microRNA 21a gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:21849676 1608349 Mir21a microRNA 21a gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:21849676 1608349 Mir21a microRNA 21a gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:21849676 1608349 Mir21a microRNA 21a gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21646541 1608349 Mir21a microRNA 21a gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20832755 1608349 Mir21a microRNA 21a gene MP:0010468 abnormal thoracic aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:23527070 1608349 Mir21a microRNA 21a gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20141003 MGI PMID:21646541 1608349 Mir21a microRNA 21a gene MP:0010945 lung epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20832755 1608349 Mir21a microRNA 21a gene MP:0011640 abnormal aorta collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:23527070 1608351 Mir18 microRNA 18 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150924 MGI PMID:26029871 1608439 Ulk4 unc-51-like kinase 4 gene MP:0000440 domed cranium IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0000440 domed cranium IAGP N RGD:5509061 20200310 MGI PMID:21746835 1608439 Ulk4 unc-51-like kinase 4 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:24284070 1608439 Ulk4 unc-51-like kinase 4 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:21746835 1608439 Ulk4 unc-51-like kinase 4 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:21746835 1608439 Ulk4 unc-51-like kinase 4 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:21746835 1608439 Ulk4 unc-51-like kinase 4 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0000917 obstructive hydrocephaly IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21746835 1608439 Ulk4 unc-51-like kinase 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:21746835 1608439 Ulk4 unc-51-like kinase 4 gene MP:0001866 nasal inflammation IAGP N RGD:5509061 20171005 MGI PMID:21746835 1608439 Ulk4 unc-51-like kinase 4 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21746835 1608439 Ulk4 unc-51-like kinase 4 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21746835 1608439 Ulk4 unc-51-like kinase 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21746835 1608439 Ulk4 unc-51-like kinase 4 gene MP:0002691 small stomach IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0002958 cerebral aqueductal stenosis IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:21746835 1608439 Ulk4 unc-51-like kinase 4 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:21746835 1608439 Ulk4 unc-51-like kinase 4 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0011057 absent brain ependyma motile cilia IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0013907 abnormal cerebrospinal fluid flow IAGP N RGD:5509061 20170112 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0014402 abnormal Reissner's fiber morphology IAGP N RGD:5509061 20240321 MGI PMID:27445138 1608439 Ulk4 unc-51-like kinase 4 gene MP:0030113 maxillary sinus inflammation IAGP N RGD:5509061 20171005 MGI PMID:21746835 1608439 Ulk4 unc-51-like kinase 4 gene MP:0030964 decreased brain ependyma motile cilium length IAGP N RGD:5509061 20190725 MGI PMID:21746835 1608452 Rnf169 ring finger protein 169 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20141003 MGI 1608452 Rnf169 ring finger protein 169 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20160804 MGI 1608452 Rnf169 ring finger protein 169 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20160804 MGI 1608452 Rnf169 ring finger protein 169 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20141003 MGI 1608745 2700054A10Rik RIKEN cDNA 2700054A10 gene gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1608745 2700054A10Rik RIKEN cDNA 2700054A10 gene gene MP:0001293 anophthalmia IEA N RGD:5509061 20181227 MGI 1608745 2700054A10Rik RIKEN cDNA 2700054A10 gene gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1608745 2700054A10Rik RIKEN cDNA 2700054A10 gene gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20240523 MGI 1608745 2700054A10Rik RIKEN cDNA 2700054A10 gene gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1608745 2700054A10Rik RIKEN cDNA 2700054A10 gene gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1608928 Dpy19l2 dpy-19 like 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20220331 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0009839 multiflagellated sperm IAGP N RGD:5509061 20141003 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0031372 abnormal sperm individualization IAGP N RGD:5509061 20220331 MGI PMID:22764053 1608928 Dpy19l2 dpy-19 like 2 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20220428 MGI PMID:22764053 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:21857657 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20230427 MGI PMID:35868558 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21857657 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:21857657 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230427 MGI PMID:35868558 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:21857657 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20230427 MGI PMID:35868558 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20230427 MGI PMID:35868558 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21857657 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21857657 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21857657 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:21857657 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21857657 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21857657 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20230427 MGI PMID:35868558 1608991 Mir124a-1hg Mir124-1 host gene (non-protein coding) gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230427 MGI PMID:35868558 1609124 Gata3un Gata3 upstream neighbor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230126 MGI PMID:29420831 1609478 Ajap1 adherens junction associated protein 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1609478 Ajap1 adherens junction associated protein 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 1609478 Ajap1 adherens junction associated protein 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1609478 Ajap1 adherens junction associated protein 1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 1609478 Ajap1 adherens junction associated protein 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160421 MGI 1609478 Ajap1 adherens junction associated protein 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220519 MGI 1609478 Ajap1 adherens junction associated protein 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1609478 Ajap1 adherens junction associated protein 1 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 1609478 Ajap1 adherens junction associated protein 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 1609478 Ajap1 adherens junction associated protein 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1609478 Ajap1 adherens junction associated protein 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1609478 Ajap1 adherens junction associated protein 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220519 MGI 1609552 Hand2os1 Hand2, opposite strand 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190919 MGI PMID:27783597 1609552 Hand2os1 Hand2, opposite strand 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230126 MGI PMID:29420831 1609552 Hand2os1 Hand2, opposite strand 1 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20230126 MGI PMID:29420831 1609552 Hand2os1 Hand2, opposite strand 1 gene MP:0003872 absent heart right ventricle IAGP N RGD:5509061 20190919 MGI PMID:27783597 1609552 Hand2os1 Hand2, opposite strand 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20190919 MGI PMID:27783597 1609552 Hand2os1 Hand2, opposite strand 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20190919 MGI PMID:27783597 1609552 Hand2os1 Hand2, opposite strand 1 gene MP:0010432 common ventricle IAGP N RGD:5509061 20190919 MGI PMID:27783597 1609552 Hand2os1 Hand2, opposite strand 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20230126 MGI PMID:29420831 1609552 Hand2os1 Hand2, opposite strand 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20190919 MGI PMID:27783597 1609552 Hand2os1 Hand2, opposite strand 1 gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20190919 MGI PMID:27783597 1609618 Btnl6 butyrophilin-like 6 gene MP:0008359 decreased CD4-positive, gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20231109 MGI PMID:32724083 1609759 Pldi polymorphic derived intron containing gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19733073 1609759 Pldi polymorphic derived intron containing gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19733073 1609826 1600029I14Rik RIKEN cDNA 1600029I14 gene gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1609826 1600029I14Rik RIKEN cDNA 1600029I14 gene gene MP:0004930 small epididymis IEA N RGD:5509061 20200514 MGI 1609846 Gata6os GATA binding protein 6, opposite strand gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20191107 MGI PMID:30224759 1609846 Gata6os GATA binding protein 6, opposite strand gene MP:0001661 extended life span IAGP N RGD:5509061 20191107 MGI PMID:30224759 1609846 Gata6os GATA binding protein 6, opposite strand gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230126 MGI PMID:29420831 1609846 Gata6os GATA binding protein 6, opposite strand gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20191107 MGI PMID:30224759 1609846 Gata6os GATA binding protein 6, opposite strand gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20191107 MGI PMID:30224759 1609846 Gata6os GATA binding protein 6, opposite strand gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20191107 MGI PMID:30224759 1609846 Gata6os GATA binding protein 6, opposite strand gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20191107 MGI PMID:30224759 1609846 Gata6os GATA binding protein 6, opposite strand gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20191107 MGI PMID:30224759 1609846 Gata6os GATA binding protein 6, opposite strand gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20191107 MGI PMID:30224759 1609846 Gata6os GATA binding protein 6, opposite strand gene MP:0012734 abnormal response to radiation IAGP N RGD:5509061 20191107 MGI PMID:30224759 1609892 Fnip2 folliculin interacting protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170525 MGI PMID:25775561 1609892 Fnip2 folliculin interacting protein 2 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20170525 MGI PMID:25775561 1609892 Fnip2 folliculin interacting protein 2 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20170525 MGI PMID:25775561 1609892 Fnip2 folliculin interacting protein 2 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20170525 MGI PMID:25775561 1609892 Fnip2 folliculin interacting protein 2 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1609892 Fnip2 folliculin interacting protein 2 gene MP:0010294 increased kidney tumor incidence IAGP N RGD:5509061 20170525 MGI PMID:25775561 1609892 Fnip2 folliculin interacting protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170525 MGI PMID:25775561 1609948 Sros1 non-coding RNA suppressor of Stat1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20210701 MGI PMID:31740800 1609948 Sros1 non-coding RNA suppressor of Stat1 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20210701 MGI PMID:31740800 1609948 Sros1 non-coding RNA suppressor of Stat1 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20210701 MGI PMID:31740800 1609948 Sros1 non-coding RNA suppressor of Stat1 gene MP:0031220 increased circulating CXCL10 level IAGP N RGD:5509061 20210701 MGI PMID:31740800 1610154 Platr4 pluripotency associated transcript 4 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20221215 MGI PMID:36347239 1610154 Platr4 pluripotency associated transcript 4 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20221215 MGI PMID:36347239 1610154 Platr4 pluripotency associated transcript 4 gene MP:0002083 premature death IAGP N RGD:5509061 20221215 MGI PMID:36347239 1610154 Platr4 pluripotency associated transcript 4 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20221215 MGI PMID:36347239 1610154 Platr4 pluripotency associated transcript 4 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20221215 MGI PMID:36347239 1610154 Platr4 pluripotency associated transcript 4 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20221215 MGI PMID:36347239 1610154 Platr4 pluripotency associated transcript 4 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20221215 MGI PMID:36347239 1610154 Platr4 pluripotency associated transcript 4 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20221215 MGI PMID:36347239 1610154 Platr4 pluripotency associated transcript 4 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20221215 MGI PMID:36347239 1610154 Platr4 pluripotency associated transcript 4 gene MP:0006431 abnormal fibrocartilage morphology IAGP N RGD:5509061 20221215 MGI PMID:36347239 1610154 Platr4 pluripotency associated transcript 4 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20221215 MGI PMID:36347239 1610182 Redrum Redrum, erythroid developmental long intergenic non-protein coding transcript gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200806 MGI PMID:29237115 1610387 Atcayos ataxia, cerebellar, Cayman type, opposite strand gene MP:0003916 decreased heart left ventricle weight IAGP N RGD:5509061 20200402 MGI PMID:31784461 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0000753 paralysis IAGP N RGD:5509061 20180201 MGI PMID:12084935 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20180201 MGI PMID:12084935 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0001393 ataxia IAGP N RGD:5509061 20180201 MGI PMID:12084935 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20241114 MGI PMID:31237944 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0001523 impaired righting response IAGP N RGD:5509061 20180201 MGI PMID:12084935 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0001661 extended life span IAGP N RGD:5509061 20241114 MGI PMID:31237944 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20180201 MGI PMID:12084935 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:12084935 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0002083 premature death IAGP N RGD:5509061 20241114 MGI PMID:31237944 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20180201 MGI PMID:12084935 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20241114 MGI PMID:31237944 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20241114 MGI PMID:31237944 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20180201 MGI PMID:12084935 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20241114 MGI PMID:31237944 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0003354 astrocytosis IAGP N RGD:5509061 20180201 MGI PMID:12084935 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0003354 astrocytosis IAGP N RGD:5509061 20241114 MGI PMID:31237944 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20180201 MGI PMID:12084935 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20180201 MGI PMID:12084935 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0005156 bradykinesia IAGP N RGD:5509061 20180201 MGI PMID:12084935 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0005323 dystonia IAGP N RGD:5509061 20180201 MGI PMID:12084935 1610393 2310039L15Rik RIKEN cDNA 2310039L15 gene gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20241114 MGI PMID:31237944 1610443 Ccdc180 coiled-coil domain containing 180 gene MP:0001925 male infertility IEA N RGD:5509061 20240523 MGI 1610443 Ccdc180 coiled-coil domain containing 180 gene MP:0001926 female infertility IEA N RGD:5509061 20240523 MGI 1610443 Ccdc180 coiled-coil domain containing 180 gene MP:0005543 decreased cornea thickness IEA N RGD:5509061 20240523 MGI 1610450 Trim67 tripartite motif-containing 67 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0008222 decreased hippocampal commissure size IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0012462 decreased brain internal capsule size IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0012480 decreased amygdala size IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0013908 small lateral ventricles IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0014114 abnormal cognition IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0014115 cognitive inflexibility IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0020527 small thalamus IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610450 Trim67 tripartite motif-containing 67 gene MP:0020554 decreased stria medullaris size IAGP N RGD:5509061 20181220 MGI PMID:29911180 1610489 Leat1 lncRNA Efnb2 associated transcript 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200430 MGI PMID:31830612 1610489 Leat1 lncRNA Efnb2 associated transcript 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200430 MGI PMID:31830612 1610489 Leat1 lncRNA Efnb2 associated transcript 1 gene MP:0003550 short perineum IAGP N RGD:5509061 20200430 MGI PMID:31830612 1610489 Leat1 lncRNA Efnb2 associated transcript 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20200430 MGI PMID:31830612 1610800 1700069L16Rik RIKEN cDNA 1700069L16 gene gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220811 MGI 1610800 1700069L16Rik RIKEN cDNA 1700069L16 gene gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220811 MGI 1610800 1700069L16Rik RIKEN cDNA 1700069L16 gene gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220811 MGI 1610866 Krt28 keratin 28 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1610866 Krt28 keratin 28 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210520 MGI 1610866 Krt28 keratin 28 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1610875 Mir205hg Mir205 host gene gene MP:0000706 small thymus IAGP N RGD:5509061 20190919 MGI PMID:30982661 1610875 Mir205hg Mir205 host gene gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20190919 MGI PMID:30982661 1610875 Mir205hg Mir205 host gene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190919 MGI PMID:30982661 1610875 Mir205hg Mir205 host gene gene MP:0001265 decreased body size IAGP N RGD:5509061 20190919 MGI PMID:30982661 1610875 Mir205hg Mir205 host gene gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20190919 MGI PMID:30982661 1610875 Mir205hg Mir205 host gene gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20190919 MGI PMID:30982661 1610875 Mir205hg Mir205 host gene gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20190919 MGI PMID:30982661 1610875 Mir205hg Mir205 host gene gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20190919 MGI PMID:30982661 1610900 Fcor Foxo1 corepressor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22510882 1610900 Fcor Foxo1 corepressor gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22510882 1610900 Fcor Foxo1 corepressor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22510882 1610900 Fcor Foxo1 corepressor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22510882 1610900 Fcor Foxo1 corepressor gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22510882 1610900 Fcor Foxo1 corepressor gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22510882 1610909 Neat1 nuclear paraspeckle assembly transcript 1 (non-protein coding) gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20160211 MGI PMID:25316907 1610909 Neat1 nuclear paraspeckle assembly transcript 1 (non-protein coding) gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20160211 MGI PMID:25316907 1610909 Neat1 nuclear paraspeckle assembly transcript 1 (non-protein coding) gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20160211 MGI PMID:25316907 1610909 Neat1 nuclear paraspeckle assembly transcript 1 (non-protein coding) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160211 MGI PMID:25316907 1610909 Neat1 nuclear paraspeckle assembly transcript 1 (non-protein coding) gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20160211 MGI PMID:25316907 1610909 Neat1 nuclear paraspeckle assembly transcript 1 (non-protein coding) gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:21444682 1610909 Neat1 nuclear paraspeckle assembly transcript 1 (non-protein coding) gene MP:0003718 maternal effect IAGP N RGD:5509061 20160211 MGI PMID:25316907 1610909 Neat1 nuclear paraspeckle assembly transcript 1 (non-protein coding) gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20160211 MGI PMID:25316907 1610909 Neat1 nuclear paraspeckle assembly transcript 1 (non-protein coding) gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20160211 MGI PMID:25316907 1610909 Neat1 nuclear paraspeckle assembly transcript 1 (non-protein coding) gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20160211 MGI PMID:25316907 1610909 Neat1 nuclear paraspeckle assembly transcript 1 (non-protein coding) gene MP:0011940 decreased food intake IAGP N RGD:5509061 20160211 MGI PMID:25316907 1610965 Gpr62 G protein-coupled receptor 62 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:28912303 1610968 Ptprh protein tyrosine phosphatase receptor type H gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:19170756 1611166 Mir142hg Mir142 host gene (non-protein coding) gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141009 MGI PMID:24352241 1611166 Mir142hg Mir142 host gene (non-protein coding) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141009 MGI PMID:24352241 1611166 Mir142hg Mir142 host gene (non-protein coding) gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141009 MGI PMID:24352241 1611166 Mir142hg Mir142 host gene (non-protein coding) gene MP:0005461 abnormal dendritic cell morphology IAGP N RGD:5509061 20141009 MGI PMID:24352241 1611166 Mir142hg Mir142 host gene (non-protein coding) gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141009 MGI PMID:24352241 1611166 Mir142hg Mir142 host gene (non-protein coding) gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141009 MGI PMID:24352241 1611166 Mir142hg Mir142 host gene (non-protein coding) gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141009 MGI PMID:24352241 1611166 Mir142hg Mir142 host gene (non-protein coding) gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141009 MGI PMID:24352241 1611244 Hdnr Hand2 downstream lncRNA gene MP:0003916 decreased heart left ventricle weight IAGP N RGD:5509061 20200402 MGI PMID:31784461 1611244 Hdnr Hand2 downstream lncRNA gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20200402 MGI PMID:31784461 1611244 Hdnr Hand2 downstream lncRNA gene MP:0005629 abnormal lung weight IAGP N RGD:5509061 20200402 MGI PMID:31784461 1611458 Ildr2 immunoglobulin-like domain containing receptor 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:18654634 1611458 Ildr2 immunoglobulin-like domain containing receptor 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18654634 1611458 Ildr2 immunoglobulin-like domain containing receptor 2 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:18654634 1611458 Ildr2 immunoglobulin-like domain containing receptor 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18654634 1611458 Ildr2 immunoglobulin-like domain containing receptor 2 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:18654634 1611458 Ildr2 immunoglobulin-like domain containing receptor 2 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18654634 1611478 Baiap3 BAI1-associated protein 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20151001 MGI PMID:23698091 1611478 Baiap3 BAI1-associated protein 3 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20151001 MGI PMID:23698091 1611478 Baiap3 BAI1-associated protein 3 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20151001 MGI PMID:23698091 1611478 Baiap3 BAI1-associated protein 3 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20151001 MGI PMID:23698091 1611478 Baiap3 BAI1-associated protein 3 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20151001 MGI PMID:23698091 1611478 Baiap3 BAI1-associated protein 3 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20151001 MGI PMID:23698091 1611478 Baiap3 BAI1-associated protein 3 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20151001 MGI PMID:23698091 1611478 Baiap3 BAI1-associated protein 3 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:23698091 1611507 Lcn6 lipocalin 6 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20180329 MGI PMID:29045572 1611507 Lcn6 lipocalin 6 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20180329 MGI PMID:29045572 1611507 Lcn6 lipocalin 6 gene MP:0013288 premature acrosome reaction IAGP N RGD:5509061 20180329 MGI PMID:29045572 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:16033881 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20180201 MGI PMID:25176149 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200123 MGI PMID:31285329 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200123 MGI PMID:31285329 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20180201 MGI PMID:16033881 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:19630976 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20180201 MGI PMID:16033881 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20200123 MGI PMID:31285329 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20180201 MGI PMID:26869263 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20200123 MGI PMID:31285329 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20180201 MGI PMID:25176149 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20180201 MGI PMID:16033881 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20180201 MGI PMID:26869263 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20200123 MGI PMID:31285329 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200123 MGI PMID:31285329 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20180201 MGI PMID:16033881 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20180201 MGI PMID:19630976 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0005665 increased circulating noradrenaline level IAGP N RGD:5509061 20180201 MGI PMID:19630976 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20200123 MGI PMID:31285329 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20200123 MGI PMID:31285329 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0009016 abnormal estrus IAGP N RGD:5509061 20200123 MGI PMID:31285329 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:19630976 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20180920 MGI PMID:19630976 1611742 7630403G23Rik RIKEN cDNA 7630403G23 gene gene MP:0020543 decreased substantia nigra size IAGP N RGD:5509061 20180301 MGI PMID:16033881 1611791 Fam227b family with sequence similarity 227, member B gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0000495 abnormal colon morphology IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0001925 male infertility IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0001926 female infertility IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0002581 abnormal ileum morphology IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0004002 abnormal jejunum morphology IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20230601 MGI 1611791 Fam227b family with sequence similarity 227, member B gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1611801 4930463O16Rik RIKEN cDNA 4930463O16 gene gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20221124 MGI PMID:34277642 1611801 4930463O16Rik RIKEN cDNA 4930463O16 gene gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20221124 MGI PMID:34277642 1611801 4930463O16Rik RIKEN cDNA 4930463O16 gene gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20221124 MGI PMID:34277642 1611801 4930463O16Rik RIKEN cDNA 4930463O16 gene gene MP:0031426 increased sperm motility IAGP N RGD:5509061 20221124 MGI PMID:34277642 1611801 4930463O16Rik RIKEN cDNA 4930463O16 gene gene MP:0031427 increased sperm progressive motility IAGP N RGD:5509061 20221124 MGI PMID:34277642 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20233966 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220519 MGI 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0000274 enlarged heart IEA N RGD:5509061 20220519 MGI 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220519 MGI 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220519 MGI 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20233966 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20233966 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20233966 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20233966 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20220519 MGI 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20240523 MGI 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20220519 MGI 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20220519 MGI 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20220519 MGI 1611829 Lrrc17 leucine rich repeat containing 17 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20220519 MGI 1611847 Dino damage induced long noncoding RNA gene MP:0003010 decreased mortality induced by ionizing radiation IAGP N RGD:5509061 20220922 MGI PMID:27668660 1611847 Dino damage induced long noncoding RNA gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20220922 MGI PMID:27668660 1611847 Dino damage induced long noncoding RNA gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20220922 MGI PMID:27668660 1611847 Dino damage induced long noncoding RNA gene MP:0014042 decreased cellular sensitivity to DNA damaging agents IAGP N RGD:5509061 20220922 MGI PMID:27668660 1611867 Ptchd4 patched domain containing 4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1611867 Ptchd4 patched domain containing 4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1611867 Ptchd4 patched domain containing 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1611867 Ptchd4 patched domain containing 4 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 1611867 Ptchd4 patched domain containing 4 gene MP:0011044 increased lung elastance IEA N RGD:5509061 20231207 MGI 1611912 Lelp1 late cornified envelope-like proline-rich 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20240523 MGI 1611912 Lelp1 late cornified envelope-like proline-rich 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 1611912 Lelp1 late cornified envelope-like proline-rich 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20240523 MGI 1611912 Lelp1 late cornified envelope-like proline-rich 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20240523 MGI 1611912 Lelp1 late cornified envelope-like proline-rich 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201022 MGI PMID:32588039 1611912 Lelp1 late cornified envelope-like proline-rich 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 1611959 Ms4a12 membrane-spanning 4-domains, subfamily A, member 12 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1611959 Ms4a12 membrane-spanning 4-domains, subfamily A, member 12 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1611959 Ms4a12 membrane-spanning 4-domains, subfamily A, member 12 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220519 MGI 1612156 Lhx1os LIM homeobox 1, opposite strand gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230126 MGI PMID:29420831 1612159 2500002B13Rik RIKEN cDNA 2500002B13 gene gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20211104 MGI PMID:33953175 1612159 2500002B13Rik RIKEN cDNA 2500002B13 gene gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20211104 MGI PMID:33953175 1612159 2500002B13Rik RIKEN cDNA 2500002B13 gene gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20211104 MGI PMID:33953175 1612159 2500002B13Rik RIKEN cDNA 2500002B13 gene gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20211104 MGI PMID:33953175 1612159 2500002B13Rik RIKEN cDNA 2500002B13 gene gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20211104 MGI PMID:33953175 1612204 Mpped2 metallophosphoesterase domain containing 2 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1612204 Mpped2 metallophosphoesterase domain containing 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 1612289 Evx1os even skipped homeotic gene 1, opposite strand gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230126 MGI PMID:29420831 1612333 Pantr2 POU domain, class 3, transcription factor 3 adjacent noncoding transcript 2 gene MP:0000861 disorganized barrel cortex IAGP N RGD:5509061 20141003 MGI PMID:24381249 1612333 Pantr2 POU domain, class 3, transcription factor 3 adjacent noncoding transcript 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24381249 1612333 Pantr2 POU domain, class 3, transcription factor 3 adjacent noncoding transcript 2 gene MP:0003989 abnormal barrel cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:24381249 1612333 Pantr2 POU domain, class 3, transcription factor 3 adjacent noncoding transcript 2 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:24381249 1612333 Pantr2 POU domain, class 3, transcription factor 3 adjacent noncoding transcript 2 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:24381249 1612333 Pantr2 POU domain, class 3, transcription factor 3 adjacent noncoding transcript 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:24381249 1612333 Pantr2 POU domain, class 3, transcription factor 3 adjacent noncoding transcript 2 gene MP:0020069 decreased neocortex size IAGP N RGD:5509061 20141003 MGI PMID:24381249 1612334 Oip5os1 Opa interacting protein 5, opposite strand 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190523 MGI PMID:29887379 1612334 Oip5os1 Opa interacting protein 5, opposite strand 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230126 MGI PMID:29420831 1612354 Rn7sk RNA, 7SK, nuclear gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20221208 MGI PMID:34620876 1612354 Rn7sk RNA, 7SK, nuclear gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20221208 MGI PMID:34620876 1612360 Nrg2 neuregulin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15340081 1612360 Nrg2 neuregulin 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15340081 1612360 Nrg2 neuregulin 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15340081 1612412 Map3k15 mitogen-activated protein kinase kinase kinase 15 gene MP:0000231 hypertension IAGP N RGD:5509061 20151022 MGI PMID:23250415 1612412 Map3k15 mitogen-activated protein kinase kinase kinase 15 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20151022 MGI PMID:23250415 1612412 Map3k15 mitogen-activated protein kinase kinase kinase 15 gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20151022 MGI PMID:23250415 1612412 Map3k15 mitogen-activated protein kinase kinase kinase 15 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20151022 MGI PMID:23250415 1612412 Map3k15 mitogen-activated protein kinase kinase kinase 15 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20151022 MGI PMID:23250415 1612419 Cog5 component of oligomeric golgi complex 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1612419 Cog5 component of oligomeric golgi complex 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1612419 Cog5 component of oligomeric golgi complex 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1612419 Cog5 component of oligomeric golgi complex 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1612419 Cog5 component of oligomeric golgi complex 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1612419 Cog5 component of oligomeric golgi complex 5 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230601 MGI 1612419 Cog5 component of oligomeric golgi complex 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1612419 Cog5 component of oligomeric golgi complex 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20240523 MGI 1612419 Cog5 component of oligomeric golgi complex 5 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20240523 MGI 1612419 Cog5 component of oligomeric golgi complex 5 gene MP:0020422 decreased freezing behavior IEA N RGD:5509061 20230601 MGI 1612423 Dbx2 developing brain homeobox 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1612423 Dbx2 developing brain homeobox 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20220407 MGI PMID:33497014 1612425 Rnf157 ring finger protein 157 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1612425 Rnf157 ring finger protein 157 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1612425 Rnf157 ring finger protein 157 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25342469 1612425 Rnf157 ring finger protein 157 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1612426 Tent5d terminal nucleotidyltransferase 5D gene MP:0001925 male infertility IAGP N RGD:5509061 20230817 MGI PMID:35256600 1612426 Tent5d terminal nucleotidyltransferase 5D gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230817 MGI PMID:35256600 1612426 Tent5d terminal nucleotidyltransferase 5D gene MP:0002686 globozoospermia IAGP N RGD:5509061 20230817 MGI PMID:35256600 1612426 Tent5d terminal nucleotidyltransferase 5D gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230817 MGI PMID:35256600 1612426 Tent5d terminal nucleotidyltransferase 5D gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20230817 MGI PMID:35256600 1612426 Tent5d terminal nucleotidyltransferase 5D gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20230817 MGI PMID:35256600 1612491 Pax1dt paired box 1 divergent transcript gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240328 MGI PMID:27986952 1612607 Pabpc1l poly(A) binding protein, cytoplasmic 1-like gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:22621333 1612607 Pabpc1l poly(A) binding protein, cytoplasmic 1-like gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22621333 1612607 Pabpc1l poly(A) binding protein, cytoplasmic 1-like gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:22621333 1612607 Pabpc1l poly(A) binding protein, cytoplasmic 1-like gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:22621333 1612607 Pabpc1l poly(A) binding protein, cytoplasmic 1-like gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:22621333 1612607 Pabpc1l poly(A) binding protein, cytoplasmic 1-like gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:22621333 1612607 Pabpc1l poly(A) binding protein, cytoplasmic 1-like gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:22621333 1612607 Pabpc1l poly(A) binding protein, cytoplasmic 1-like gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1612607 Pabpc1l poly(A) binding protein, cytoplasmic 1-like gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22621333 1612607 Pabpc1l poly(A) binding protein, cytoplasmic 1-like gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20220407 MGI PMID:22621333 1612607 Pabpc1l poly(A) binding protein, cytoplasmic 1-like gene MP:0011701 decreased cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:22621333 1612607 Pabpc1l poly(A) binding protein, cytoplasmic 1-like gene MP:0014445 abnormal spindle assembly in female meiosis IAGP N RGD:5509061 20240509 MGI PMID:22621333 1612607 Pabpc1l poly(A) binding protein, cytoplasmic 1-like gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:22621333 1612622 Rab26os RAB26, member RAS oncogene family, opposite strand gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230126 MGI PMID:29420831 1612971 Flicr Foxp3 regulating long intergenic noncoding RNA gene MP:0004031 insulitis IAGP N RGD:5509061 20170921 MGI PMID:28396406 1612971 Flicr Foxp3 regulating long intergenic noncoding RNA gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20170921 MGI PMID:28396406 1612991 4930404H24Rik RIKEN cDNA 4930404H24 gene gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 1612991 4930404H24Rik RIKEN cDNA 4930404H24 gene gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1613143 4833411C07Rik RIKEN cDNA 4833411C07 gene gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210506 MGI PMID:32005828 1613143 4833411C07Rik RIKEN cDNA 4833411C07 gene gene MP:0005331 insulin resistance IAGP N RGD:5509061 20210506 MGI PMID:32005828 1613143 4833411C07Rik RIKEN cDNA 4833411C07 gene gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20210506 MGI PMID:32005828 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210211 MGI PMID:32891704 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0001401 jumpy IAGP N RGD:5509061 20170309 MGI PMID:28007585 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210211 MGI PMID:32891704 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20170309 MGI PMID:28007585 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0001454 abnormal cued conditioning behavior IEA N RGD:5509061 20210128 MGI 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20181227 MGI 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20170309 MGI PMID:28007585 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20210211 MGI PMID:32891704 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20170309 MGI PMID:28007585 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20170309 MGI PMID:28007585 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20170309 MGI PMID:28007585 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20210211 MGI PMID:32891704 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20170309 MGI PMID:28007585 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20170309 MGI PMID:28007585 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20170309 MGI PMID:28007585 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0005323 dystonia IAGP N RGD:5509061 20210211 MGI PMID:32891704 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0005424 jerky movement IAGP N RGD:5509061 20170309 MGI PMID:28007585 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20170309 MGI PMID:28007585 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20170309 MGI PMID:28007585 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20210211 MGI PMID:32891704 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0010323 retropulsion IAGP N RGD:5509061 20170309 MGI PMID:28007585 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20210211 MGI PMID:32891704 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20170309 MGI PMID:28007585 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0020358 abnormal inhibitory synapse morphology IAGP N RGD:5509061 20170309 MGI PMID:28007585 1613176 Prrt2 proline-rich transmembrane protein 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:32891704 1613196 Klra15 killer cell lectin-like receptor, subfamily A, member 15 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:22661698 1613284 Gcnt4 glucosaminyl (N-acetyl) transferase 4, core 2 (beta-1,6-N-acetylglucosaminyltransferase) gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19349303 1613284 Gcnt4 glucosaminyl (N-acetyl) transferase 4, core 2 (beta-1,6-N-acetylglucosaminyltransferase) gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:19349303 1613284 Gcnt4 glucosaminyl (N-acetyl) transferase 4, core 2 (beta-1,6-N-acetylglucosaminyltransferase) gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:19349303 1613284 Gcnt4 glucosaminyl (N-acetyl) transferase 4, core 2 (beta-1,6-N-acetylglucosaminyltransferase) gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19349303 1613284 Gcnt4 glucosaminyl (N-acetyl) transferase 4, core 2 (beta-1,6-N-acetylglucosaminyltransferase) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19349303 1613284 Gcnt4 glucosaminyl (N-acetyl) transferase 4, core 2 (beta-1,6-N-acetylglucosaminyltransferase) gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:19349303 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0000111 cleft palate IAGP N RGD:5509061 20200514 MGI PMID:31600785 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141120 MGI PMID:24753090 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20141120 MGI PMID:24753090 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:19922873 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141120 MGI PMID:24753090 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:19922873 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141120 MGI PMID:24753090 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200514 MGI PMID:31600785 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200514 MGI PMID:31600785 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20170105 MGI PMID:27297885 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20170105 MGI PMID:27297885 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190808 MGI 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18454205 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141120 MGI PMID:24753090 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200514 MGI PMID:31600785 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141120 MGI PMID:24753090 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20170105 MGI 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20170105 MGI PMID:27297885 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20170105 MGI PMID:27297885 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20170105 MGI PMID:27297885 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0005072 abnormal hair follicle melanin granule morphology IAGP N RGD:5509061 20141120 MGI PMID:24753090 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0005174 abnormal tail pigmentation IAGP N RGD:5509061 20180719 MGI PMID:29781574 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0009387 abnormal epidermal pigmentation IAGP N RGD:5509061 20180719 MGI PMID:29781574 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:18454205 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20141120 MGI PMID:24753090 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20180719 MGI PMID:29781574 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141120 MGI PMID:24753090 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18454205 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200514 MGI PMID:31600785 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18454205 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19922873 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141120 MGI PMID:24753090 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141120 MGI PMID:24753090 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:29781574 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20170105 MGI PMID:27297885 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20170105 MGI PMID:27297885 1613350 Adamts9 ADAM metallopeptidase with thrombospondin type 1 motif 9 gene MP:0030911 increased melanoblast apoptosis IAGP N RGD:5509061 20190411 MGI PMID:29781574 1613514 2310065F04Rik RIKEN cDNA 2310065F04 gene gene MP:0000730 increased satellite cell number IAGP N RGD:5509061 20240620 MGI PMID:32960481 1613514 2310065F04Rik RIKEN cDNA 2310065F04 gene gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20240620 MGI PMID:32960481 1613514 2310065F04Rik RIKEN cDNA 2310065F04 gene gene MP:0001260 increased body weight IAGP N RGD:5509061 20240620 MGI PMID:32960481 1613514 2310065F04Rik RIKEN cDNA 2310065F04 gene gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20240620 MGI PMID:32960481 1613514 2310065F04Rik RIKEN cDNA 2310065F04 gene gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20240620 MGI PMID:32960481 1613514 2310065F04Rik RIKEN cDNA 2310065F04 gene gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20240620 MGI PMID:32960481 1613514 2310065F04Rik RIKEN cDNA 2310065F04 gene gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20240620 MGI PMID:32960481 1613514 2310065F04Rik RIKEN cDNA 2310065F04 gene gene MP:0010238 increased skeletal muscle weight IAGP N RGD:5509061 20240620 MGI PMID:32960481 1613514 2310065F04Rik RIKEN cDNA 2310065F04 gene gene MP:0031323 increased skeletal muscle satellite cell proliferation IAGP N RGD:5509061 20240620 MGI PMID:32960481 1613557 9030622O22Rik RIKEN cDNA 9030622O22 gene gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200402 MGI PMID:30923168 1613557 9030622O22Rik RIKEN cDNA 9030622O22 gene gene MP:0002281 abnormal respiratory mucosa goblet cell morphology IAGP N RGD:5509061 20200402 MGI PMID:30923168 1613557 9030622O22Rik RIKEN cDNA 9030622O22 gene gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20200402 MGI PMID:30923168 1613557 9030622O22Rik RIKEN cDNA 9030622O22 gene gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20200402 MGI PMID:30923168 1613572 Piezo2 piezo-type mechanosensitive ion channel component 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20190509 MGI PMID:30305456 1613572 Piezo2 piezo-type mechanosensitive ion channel component 2 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20220811 MGI 1613572 Piezo2 piezo-type mechanosensitive ion channel component 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210128 MGI 1613572 Piezo2 piezo-type mechanosensitive ion channel component 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20190509 MGI PMID:30305456 1613572 Piezo2 piezo-type mechanosensitive ion channel component 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:24717433 1613572 Piezo2 piezo-type mechanosensitive ion channel component 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1613572 Piezo2 piezo-type mechanosensitive ion channel component 2 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:24717433 1613572 Piezo2 piezo-type mechanosensitive ion channel component 2 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20190509 MGI PMID:30305456 1613572 Piezo2 piezo-type mechanosensitive ion channel component 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1613572 Piezo2 piezo-type mechanosensitive ion channel component 2 gene MP:0012001 abnormal touch escape response IAGP N RGD:5509061 20190509 MGI PMID:30305456 1613633 Bbip1 BBSome interacting protein 1 gene MP:0000160 kyphosis IEA N RGD:5509061 20210826 MGI 1613633 Bbip1 BBSome interacting protein 1 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:24316073 1613633 Bbip1 BBSome interacting protein 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:24316073 1613633 Bbip1 BBSome interacting protein 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:24316073 1613633 Bbip1 BBSome interacting protein 1 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210826 MGI 1613633 Bbip1 BBSome interacting protein 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:24316073 1613633 Bbip1 BBSome interacting protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:24316073 1613633 Bbip1 BBSome interacting protein 1 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210826 MGI 1613633 Bbip1 BBSome interacting protein 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1613633 Bbip1 BBSome interacting protein 1 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20210826 MGI 1613633 Bbip1 BBSome interacting protein 1 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20210826 MGI 1613633 Bbip1 BBSome interacting protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24316073 1613633 Bbip1 BBSome interacting protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24316073 1613633 Bbip1 BBSome interacting protein 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:24316073 1613682 Ccdc85c coiled-coil domain containing 85C gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20180412 MGI PMID:15283996 1613682 Ccdc85c coiled-coil domain containing 85C gene MP:0000804 abnormal occipital lobe morphology IAGP N RGD:5509061 20180412 MGI PMID:15283996 1613682 Ccdc85c coiled-coil domain containing 85C gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20180412 MGI PMID:15283996 1613682 Ccdc85c coiled-coil domain containing 85C gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20180412 MGI PMID:15283996 1613682 Ccdc85c coiled-coil domain containing 85C gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20180412 MGI PMID:15283996 1613682 Ccdc85c coiled-coil domain containing 85C gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20180412 MGI PMID:15283996 1613682 Ccdc85c coiled-coil domain containing 85C gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20180412 MGI PMID:15283996 1613682 Ccdc85c coiled-coil domain containing 85C gene MP:0002083 premature death IAGP N RGD:5509061 20180412 MGI PMID:15283996 1613682 Ccdc85c coiled-coil domain containing 85C gene MP:0002183 gliosis IAGP N RGD:5509061 20180412 MGI PMID:15283996 1613682 Ccdc85c coiled-coil domain containing 85C gene MP:0002958 cerebral aqueductal stenosis IAGP N RGD:5509061 20180412 MGI PMID:15283996 1613682 Ccdc85c coiled-coil domain containing 85C gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20180412 MGI PMID:15283996 1613682 Ccdc85c coiled-coil domain containing 85C gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20180412 MGI PMID:15283996 1613701 Syce1l synaptonemal complex central element protein 1 like gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20210128 MGI 1613701 Syce1l synaptonemal complex central element protein 1 like gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20181227 MGI 1613760 Gm7694 predicted gene 7694 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1613760 Gm7694 predicted gene 7694 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220519 MGI 1613794 Trim71 tripartite motif-containing 71 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:19098426 1613794 Trim71 tripartite motif-containing 71 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19098426 1613794 Trim71 tripartite motif-containing 71 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19098426 1613794 Trim71 tripartite motif-containing 71 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:19098426 1613794 Trim71 tripartite motif-containing 71 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20160218 MGI PMID:25883935 1613794 Trim71 tripartite motif-containing 71 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20160218 MGI PMID:25883935 1613794 Trim71 tripartite motif-containing 71 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19098426 1613794 Trim71 tripartite motif-containing 71 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25883935 1613794 Trim71 tripartite motif-containing 71 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:19098426 1613794 Trim71 tripartite motif-containing 71 gene MP:0002581 abnormal ileum morphology IEA N RGD:5509061 20210128 MGI 1613794 Trim71 tripartite motif-containing 71 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:19098426 1613794 Trim71 tripartite motif-containing 71 gene MP:0004002 abnormal jejunum morphology IEA N RGD:5509061 20210128 MGI 1613794 Trim71 tripartite motif-containing 71 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:19098426 1613794 Trim71 tripartite motif-containing 71 gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:19098426 1613794 Trim71 tripartite motif-containing 71 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160218 MGI PMID:25883935 1613794 Trim71 tripartite motif-containing 71 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19098426 1613794 Trim71 tripartite motif-containing 71 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1613794 Trim71 tripartite motif-containing 71 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19098426 1613794 Trim71 tripartite motif-containing 71 gene MP:0012680 absent lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:19098426 1613794 Trim71 tripartite motif-containing 71 gene MP:0012686 everted embryonic neuroepithelium IAGP N RGD:5509061 20141003 MGI PMID:19098426 1613816 Misfa mitochondrial sheath formation associated gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20230223 MGI PMID:35228556 1613816 Misfa mitochondrial sheath formation associated gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230223 MGI PMID:35228556 1613816 Misfa mitochondrial sheath formation associated gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20230223 MGI PMID:35228556 1613816 Misfa mitochondrial sheath formation associated gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20230223 MGI PMID:35228556 1613816 Misfa mitochondrial sheath formation associated gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20230223 MGI PMID:35228556 1613887 Parp14 poly (ADP-ribose) polymerase family, member 14 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20200310 MGI PMID:19147789 1613887 Parp14 poly (ADP-ribose) polymerase family, member 14 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20200310 MGI PMID:19147789 1613887 Parp14 poly (ADP-ribose) polymerase family, member 14 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:19147789 1613887 Parp14 poly (ADP-ribose) polymerase family, member 14 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:19147789 1613887 Parp14 poly (ADP-ribose) polymerase family, member 14 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20200310 MGI PMID:19147789 1613887 Parp14 poly (ADP-ribose) polymerase family, member 14 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20200310 MGI PMID:19147789 1613887 Parp14 poly (ADP-ribose) polymerase family, member 14 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:19147789 1613897 Cers3 ceramide synthase 3 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:22038835 1613897 Cers3 ceramide synthase 3 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:22038835 1613897 Cers3 ceramide synthase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22038835 1613897 Cers3 ceramide synthase 3 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:22038835 1613897 Cers3 ceramide synthase 3 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:22038835 1613897 Cers3 ceramide synthase 3 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:22038835 1613897 Cers3 ceramide synthase 3 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22038835 1613897 Cers3 ceramide synthase 3 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20141003 MGI PMID:22038835 1613897 Cers3 ceramide synthase 3 gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:22038835 1613897 Cers3 ceramide synthase 3 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:22038835 1613897 Cers3 ceramide synthase 3 gene MP:0009596 abnormal stratum corneum lipid matrix formation IAGP N RGD:5509061 20141003 MGI PMID:22038835 1613897 Cers3 ceramide synthase 3 gene MP:0009597 impaired stratum corneum desquamation IAGP N RGD:5509061 20141003 MGI PMID:22038835 1613897 Cers3 ceramide synthase 3 gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:22038835 1613897 Cers3 ceramide synthase 3 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:22038835 1613897 Cers3 ceramide synthase 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22038835 1613907 Psg27 pregnancy-specific beta-1-glycoprotein 27 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0000111 cleft palate IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0000445 short snout IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0000562 polydactyly IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0000650 mesocardia IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20159594 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0001178 pulmonary hypoplasia IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:20159594 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0001293 anophthalmia IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0001297 microphthalmia IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:20159594 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20220519 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0001785 edema IEA N RGD:5509061 20220519 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0001914 hemorrhage IEA N RGD:5509061 20220519 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20150903 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20159594 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0002746 abnormal semilunar valve morphology IEA N RGD:5509061 20150903 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20159594 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0003178 left pulmonary isomerism IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0003321 tracheoesophageal fistula IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20220519 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0003675 kidney cyst IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20220519 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0004017 duplex kidney IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0004110 transposition of great arteries IEA N RGD:5509061 20150903 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0004113 abnormal aortic arch morphology IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0004158 right aortic arch IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20159594 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0004548 dilated esophagus IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0005170 cleft upper lip IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20159594 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0006061 right atrial isomerism IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0008461 left atrial isomerism IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0008797 facial cleft IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:20159594 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0009901 abnormal frontonasal prominence morphology IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0010460 pulmonary artery hypoplasia IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0010466 vascular ring IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0010576 premature closure of the ductus arteriosus IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0010808 right-sided stomach IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0011661 persistent truncus arteriosus type i IEA N RGD:5509061 20141003 MGI 1613911 Tbc1d32 TBC1 domain family, member 32 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20141003 MGI 1613919 Zfp141 zinc finger protein 141 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20111116 MGI PMID:12904583 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0000274 enlarged heart IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0002188 small heart IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0004937 dilated heart IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20200402 MGI 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20210520 MGI 1613941 3425401B19Rik RIKEN cDNA 3425401B19 gene gene MP:0014518 myocardial hypertrabeculation IAGP N RGD:5509061 20240926 MGI PMID:38950288 1613949 Spink7 serine peptidase inhibitor, Kazal type 7 (putative) gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20211014 MGI PMID:33722746 1613949 Spink7 serine peptidase inhibitor, Kazal type 7 (putative) gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20211014 MGI PMID:33722746 1613949 Spink7 serine peptidase inhibitor, Kazal type 7 (putative) gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20211014 MGI PMID:33722746 1613949 Spink7 serine peptidase inhibitor, Kazal type 7 (putative) gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20211014 MGI PMID:33722746 1613952 Otud6a OTU domain containing 6A gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1613952 Otud6a OTU domain containing 6A gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20190502 MGI 1613952 Otud6a OTU domain containing 6A gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20240229 MGI PMID:37632103 1613952 Otud6a OTU domain containing 6A gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1613952 Otud6a OTU domain containing 6A gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1613952 Otud6a OTU domain containing 6A gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1613952 Otud6a OTU domain containing 6A gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20240229 MGI PMID:37632103 1613952 Otud6a OTU domain containing 6A gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20240229 MGI PMID:37632103 1613985 Tas2r131 taste receptor, type 2, member 131 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1613985 Tas2r131 taste receptor, type 2, member 131 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1614007 Prdm14 PR domain containing 14 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1614007 Prdm14 PR domain containing 14 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20200402 MGI 1614007 Prdm14 PR domain containing 14 gene MP:0001399 hyperactivity IEA N RGD:5509061 20170504 MGI 1614007 Prdm14 PR domain containing 14 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18622394 1614007 Prdm14 PR domain containing 14 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18622394 1614007 Prdm14 PR domain containing 14 gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 1614007 Prdm14 PR domain containing 14 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20190502 MGI 1614007 Prdm14 PR domain containing 14 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1614007 Prdm14 PR domain containing 14 gene MP:0004806 absent germ cells IAGP N RGD:5509061 20141003 MGI PMID:18622394 1614007 Prdm14 PR domain containing 14 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1614007 Prdm14 PR domain containing 14 gene MP:0008391 abnormal primordial germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18622394 1614007 Prdm14 PR domain containing 14 gene MP:0008391 abnormal primordial germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23670199 1614007 Prdm14 PR domain containing 14 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:18622394 1614007 Prdm14 PR domain containing 14 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1614007 Prdm14 PR domain containing 14 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1614007 Prdm14 PR domain containing 14 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20220811 MGI 1614007 Prdm14 PR domain containing 14 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1614007 Prdm14 PR domain containing 14 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 1614007 Prdm14 PR domain containing 14 gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20220519 MGI 1614016 Fdxacb1 ferredoxin-fold anticodon binding domain containing 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20221215 MGI 1614016 Fdxacb1 ferredoxin-fold anticodon binding domain containing 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 1614016 Fdxacb1 ferredoxin-fold anticodon binding domain containing 1 gene MP:0001512 trunk curl IEA N RGD:5509061 20170105 MGI 1614016 Fdxacb1 ferredoxin-fold anticodon binding domain containing 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1614017 Tcaim T cell activation inhibitor, mitochondrial gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1614017 Tcaim T cell activation inhibitor, mitochondrial gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1614017 Tcaim T cell activation inhibitor, mitochondrial gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220428 MGI PMID:27811987 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20220428 MGI PMID:34704967 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20190912 MGI PMID:27811987 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20190912 MGI PMID:27811987 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220428 MGI PMID:34704967 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20190912 MGI PMID:27811987 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20220428 MGI PMID:34704967 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0004043 abnormal pH regulation IAGP N RGD:5509061 20220428 MGI PMID:34704967 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20190912 MGI PMID:27811987 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220428 MGI PMID:34704967 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20190912 MGI PMID:27811987 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20190912 MGI PMID:27811987 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20190912 MGI PMID:27811987 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220428 MGI PMID:34704967 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20190912 MGI PMID:27811987 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220428 MGI PMID:27811987 1614018 Slc22a14 solute carrier family 22 (organic cation transporter), member 14 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220428 MGI PMID:27811987 1614020 Fbxw26 F-box and WD-40 domain protein 26 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20201231 MGI 1614020 Fbxw26 F-box and WD-40 domain protein 26 gene MP:0012767 increased KLRG1-positive NK cell number IEA N RGD:5509061 20201231 MGI 1614020 Fbxw26 F-box and WD-40 domain protein 26 gene MP:0013426 decreased memory-marker NK cell number IEA N RGD:5509061 20201231 MGI 1614022 Fbxw15 F-box and WD-40 domain protein 15 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20210826 MGI 1614022 Fbxw15 F-box and WD-40 domain protein 15 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220519 MGI 1614022 Fbxw15 F-box and WD-40 domain protein 15 gene MP:0003604 single kidney IEA N RGD:5509061 20210826 MGI 1614022 Fbxw15 F-box and WD-40 domain protein 15 gene MP:0005270 abnormal zygomatic bone morphology IEA N RGD:5509061 20210826 MGI 1614022 Fbxw15 F-box and WD-40 domain protein 15 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38786026 1614026 Zfp729b zinc finger protein 729b gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 1614026 Zfp729b zinc finger protein 729b gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1614032 Mrs2 MRS2 magnesium transporter gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20210415 MGI PMID:33035451 1614032 Mrs2 MRS2 magnesium transporter gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1614032 Mrs2 MRS2 magnesium transporter gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20210415 MGI PMID:33035451 1614032 Mrs2 MRS2 magnesium transporter gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20210415 MGI PMID:33035451 1614032 Mrs2 MRS2 magnesium transporter gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20210415 MGI PMID:33035451 1614032 Mrs2 MRS2 magnesium transporter gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20210415 MGI PMID:33035451 1614032 Mrs2 MRS2 magnesium transporter gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20210415 MGI PMID:33035451 1614032 Mrs2 MRS2 magnesium transporter gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20210415 MGI PMID:33035451 1614032 Mrs2 MRS2 magnesium transporter gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20210415 MGI PMID:33035451 1614032 Mrs2 MRS2 magnesium transporter gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20210415 MGI PMID:33035451 1614037 Fndc11 fibronectin type III domain containing 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1614038 Gm5127 predicted gene 5127 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20230601 MGI 1614038 Gm5127 predicted gene 5127 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20230601 MGI 1614038 Gm5127 predicted gene 5127 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20230601 MGI 1614038 Gm5127 predicted gene 5127 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 1614038 Gm5127 predicted gene 5127 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230601 MGI 1614041 Rtl5 retrotransposon Gag like 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1614041 Rtl5 retrotransposon Gag like 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1614041 Rtl5 retrotransposon Gag like 5 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210128 MGI 1614041 Rtl5 retrotransposon Gag like 5 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20221124 MGI PMID:36162816 1614041 Rtl5 retrotransposon Gag like 5 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1614041 Rtl5 retrotransposon Gag like 5 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1614041 Rtl5 retrotransposon Gag like 5 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1614041 Rtl5 retrotransposon Gag like 5 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20221124 MGI PMID:36162816 1614041 Rtl5 retrotransposon Gag like 5 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20240523 MGI 1614042 Il1rapl1 interleukin 1 receptor accessory protein-like 1 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:19811529 1614042 Il1rapl1 interleukin 1 receptor accessory protein-like 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:19811529 1614042 Il1rapl1 interleukin 1 receptor accessory protein-like 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19811529 1614042 Il1rapl1 interleukin 1 receptor accessory protein-like 1 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20200924 MGI PMID:30838762 1614042 Il1rapl1 interleukin 1 receptor accessory protein-like 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20200924 MGI PMID:30838762 1614043 Gm773 predicted gene 773 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20211021 MGI PMID:34326397 1614043 Gm773 predicted gene 773 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20211021 MGI PMID:34326397 1614044 Thoc2 THO complex 2 gene MP:0000445 short snout IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0000447 flattened snout IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0000601 small liver IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0002188 small heart IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0003641 small lung IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0012205 abnormal neuronal stem cell self-renewal IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0014241 abnormal intracellular organelle physiology IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0014558 decreased cortical ventricular zone thickness IAGP N RGD:5509061 20241031 MGI PMID:38331934 1614044 Thoc2 THO complex 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20240905 MGI PMID:38331934 1614045 Vps37b vacuolar protein sorting 37B gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20220519 MGI 1614045 Vps37b vacuolar protein sorting 37B gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20221215 MGI 1614045 Vps37b vacuolar protein sorting 37B gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20221215 MGI 1614047 Ccdc63 coiled-coil domain containing 63 gene MP:0001925 male infertility IAGP N RGD:5509061 20191205 MGI PMID:26501274 1614047 Ccdc63 coiled-coil domain containing 63 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20191205 MGI PMID:26501274 1614047 Ccdc63 coiled-coil domain containing 63 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20191205 MGI PMID:26501274 1614047 Ccdc63 coiled-coil domain containing 63 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20191205 MGI PMID:26501274 1614047 Ccdc63 coiled-coil domain containing 63 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20191205 MGI PMID:26501274 1614047 Ccdc63 coiled-coil domain containing 63 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20191205 MGI PMID:26501274 1614048 Taok3 TAO kinase 3 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1614048 Taok3 TAO kinase 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1614048 Taok3 TAO kinase 3 gene MP:0002863 improved righting response IAGP N RGD:5509061 20220721 MGI PMID:23227189 1614048 Taok3 TAO kinase 3 gene MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20220721 MGI PMID:23227189 1614048 Taok3 TAO kinase 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20220721 MGI PMID:23227189 1614050 Kctd10 potassium channel tetramerisation domain containing 10 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20160324 MGI PMID:25401743 1614050 Kctd10 potassium channel tetramerisation domain containing 10 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20160324 MGI PMID:25401743 1614050 Kctd10 potassium channel tetramerisation domain containing 10 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20160324 MGI PMID:25401743 1614050 Kctd10 potassium channel tetramerisation domain containing 10 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20160324 MGI PMID:25401743 1614050 Kctd10 potassium channel tetramerisation domain containing 10 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20160324 MGI PMID:25401743 1614050 Kctd10 potassium channel tetramerisation domain containing 10 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20160324 MGI PMID:25401743 1614050 Kctd10 potassium channel tetramerisation domain containing 10 gene MP:0003230 abnormal umbilical artery morphology IAGP N RGD:5509061 20160324 MGI PMID:25401743 1614050 Kctd10 potassium channel tetramerisation domain containing 10 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160324 MGI PMID:25401743 1614050 Kctd10 potassium channel tetramerisation domain containing 10 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20160324 MGI PMID:25401743 1614050 Kctd10 potassium channel tetramerisation domain containing 10 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20160324 MGI PMID:25401743 1614050 Kctd10 potassium channel tetramerisation domain containing 10 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20160324 MGI PMID:25401743 1614050 Kctd10 potassium channel tetramerisation domain containing 10 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20160324 MGI PMID:25401743 1614050 Kctd10 potassium channel tetramerisation domain containing 10 gene MP:0012730 abnormal internal carotid artery morphology IAGP N RGD:5509061 20160324 MGI PMID:25401743 1614051 Miat myocardial infarction associated transcript (non-protein coding) gene MP:0001399 hyperactivity IAGP N RGD:5509061 20211014 MGI PMID:27251103 1614051 Miat myocardial infarction associated transcript (non-protein coding) gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20211014 MGI PMID:27251103 1614051 Miat myocardial infarction associated transcript (non-protein coding) gene MP:0020876 increased nervous system dopamine level IAGP N RGD:5509061 20211014 MGI PMID:27251103 1614051 Miat myocardial infarction associated transcript (non-protein coding) gene MP:0031303 enhanced behavioral response to methamphetamine IAGP N RGD:5509061 20211028 MGI PMID:27251103 1614051 Miat myocardial infarction associated transcript (non-protein coding) gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:27251103 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0009564 abnormal meiotic configurations IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614052 Hfm1 HFM1, ATP-dependent DNA helicase homolog gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23555294 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0000111 cleft palate IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0000601 small liver IAGP N RGD:5509061 20180809 MGI PMID:26446156 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0000823 abnormal lateral ventricle morphology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0000826 abnormal third ventricle morphology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0000828 abnormal fourth ventricle morphology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20180809 MGI PMID:26446156 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0001786 skin edema IAGP N RGD:5509061 20180809 MGI PMID:26446156 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20180809 MGI PMID:26446156 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0002947 increased hemangioma incidence IEA N RGD:5509061 20210930 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20180809 MGI PMID:26446156 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0003387 aorta coarctation IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0003584 bifid ureter IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0003586 dilated ureter IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0003717 pallor IAGP N RGD:5509061 20180809 MGI PMID:26446156 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20180809 MGI PMID:26446156 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0004163 abnormal adenohypophysis morphology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0004463 basisphenoid bone foramen IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0004666 absent stapedial artery IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0005244 hemopericardium IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20180809 MGI PMID:26446156 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0008922 abnormal cervical rib IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0008923 thoracoschisis IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0008986 abnormal liver parenchyma morphology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0009770 abnormal optic chiasm morphology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0010194 absent lymphatic vessels IAGP N RGD:5509061 20180809 MGI PMID:26446156 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180809 MGI PMID:26446156 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0011513 abnormal vertebral artery morphology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0011526 abnormal placenta fetal blood space morphology IAGP N RGD:5509061 20180809 MGI PMID:26446156 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0013186 abnormal basilar artery morphology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0013823 absent segment of anterior cerebral artery IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0013847 retropleural edema IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0013852 abnormal Mullerian duct topology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0013875 increased trigeminal neuroma incidence IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0013878 abnormal ductus venosus valve topology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0013968 multiple persisting craniopharyngeal ducts IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0013992 persistent dorsal ophthalmic artery IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0014019 embryo cyst IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0020483 abnormal brain artery topology IEA N RGD:5509061 20180628 MGI 1614056 Adamts3 ADAM metallopeptidase with thrombospondin type 1 motif 3 gene MP:0020500 persistent trigeminal artery IEA N RGD:5509061 20180628 MGI 1614057 Acsbg2 acyl-CoA synthetase bubblegum family member 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 1614057 Acsbg2 acyl-CoA synthetase bubblegum family member 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1614057 Acsbg2 acyl-CoA synthetase bubblegum family member 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20160804 MGI 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0001661 extended life span IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0012778 abnormal liver triglyceride level IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0020520 whitened brown adipose tissue morphology IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20190509 MGI PMID:25863250 1614069 Igf2bp2 insulin-like growth factor 2 mRNA binding protein 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:25863250 1614072 Rfx7 regulatory factor X, 7 gene MP:0000692 small spleen IAGP N RGD:5509061 20210415 MGI PMID:29967452 1614072 Rfx7 regulatory factor X, 7 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1614072 Rfx7 regulatory factor X, 7 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1614072 Rfx7 regulatory factor X, 7 gene MP:0002418 increased susceptibility to viral infection IAGP N RGD:5509061 20210415 MGI PMID:29967452 1614072 Rfx7 regulatory factor X, 7 gene MP:0005068 abnormal NK cell morphology IAGP N RGD:5509061 20210415 MGI PMID:29967452 1614072 Rfx7 regulatory factor X, 7 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20210415 MGI PMID:29967452 1614072 Rfx7 regulatory factor X, 7 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20210415 MGI PMID:29967452 1614072 Rfx7 regulatory factor X, 7 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210415 MGI PMID:29967452 1614072 Rfx7 regulatory factor X, 7 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1614075 Cacna2d4 calcium channel, voltage-dependent, alpha 2/delta subunit 4 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1614075 Cacna2d4 calcium channel, voltage-dependent, alpha 2/delta subunit 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20200402 MGI 1614075 Cacna2d4 calcium channel, voltage-dependent, alpha 2/delta subunit 4 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11053310 1614075 Cacna2d4 calcium channel, voltage-dependent, alpha 2/delta subunit 4 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11053310 1614075 Cacna2d4 calcium channel, voltage-dependent, alpha 2/delta subunit 4 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16877424 1614075 Cacna2d4 calcium channel, voltage-dependent, alpha 2/delta subunit 4 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11053310 1614075 Cacna2d4 calcium channel, voltage-dependent, alpha 2/delta subunit 4 gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11053310 1614075 Cacna2d4 calcium channel, voltage-dependent, alpha 2/delta subunit 4 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11053310 1614075 Cacna2d4 calcium channel, voltage-dependent, alpha 2/delta subunit 4 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16877424 1614075 Cacna2d4 calcium channel, voltage-dependent, alpha 2/delta subunit 4 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11053310 1614075 Cacna2d4 calcium channel, voltage-dependent, alpha 2/delta subunit 4 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11053310 1614075 Cacna2d4 calcium channel, voltage-dependent, alpha 2/delta subunit 4 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:11053310 1614075 Cacna2d4 calcium channel, voltage-dependent, alpha 2/delta subunit 4 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:16877424 1614075 Cacna2d4 calcium channel, voltage-dependent, alpha 2/delta subunit 4 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20190502 MGI 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20240530 MGI PMID:35341968 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0001925 male infertility IAGP N RGD:5509061 20210930 MGI PMID:33961623 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0001925 male infertility IAGP N RGD:5509061 20240530 MGI PMID:35341968 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210930 MGI PMID:33961623 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0005159 azoospermia IAGP N RGD:5509061 20210930 MGI PMID:33961623 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0005159 azoospermia IAGP N RGD:5509061 20240530 MGI PMID:35341968 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20210930 MGI PMID:33961623 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20240530 MGI PMID:35341968 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210930 MGI PMID:33961623 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20210930 MGI PMID:33961623 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20210930 MGI PMID:33961623 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0011953 prolonged PQ interval IEA N RGD:5509061 20231207 MGI 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20240530 MGI PMID:35341968 1614079 Kctd19 potassium channel tetramerisation domain containing 19 gene MP:0030935 increased primordial germ cell apoptosis IAGP N RGD:5509061 20210930 MGI PMID:33961623 1614085 Cdk15 cyclin dependent kinase 15 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20240523 MGI 1614085 Cdk15 cyclin dependent kinase 15 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1614089 Dagla diacylglycerol lipase, alpha gene MP:0000601 small liver IEA N RGD:5509061 20160811 MGI 1614089 Dagla diacylglycerol lipase, alpha gene MP:0000692 small spleen IEA N RGD:5509061 20160811 MGI 1614089 Dagla diacylglycerol lipase, alpha gene MP:0000706 small thymus IEA N RGD:5509061 20160811 MGI 1614089 Dagla diacylglycerol lipase, alpha gene MP:0000774 decreased brain size IEA N RGD:5509061 20160811 MGI 1614089 Dagla diacylglycerol lipase, alpha gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1614089 Dagla diacylglycerol lipase, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20147530 1614089 Dagla diacylglycerol lipase, alpha gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1614089 Dagla diacylglycerol lipase, alpha gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:20147530 1614089 Dagla diacylglycerol lipase, alpha gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:20159446 1614089 Dagla diacylglycerol lipase, alpha gene MP:0002188 small heart IEA N RGD:5509061 20160811 MGI 1614089 Dagla diacylglycerol lipase, alpha gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:21807615 1614089 Dagla diacylglycerol lipase, alpha gene MP:0002691 small stomach IEA N RGD:5509061 20160811 MGI 1614089 Dagla diacylglycerol lipase, alpha gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21613483 1614089 Dagla diacylglycerol lipase, alpha gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20147530 1614089 Dagla diacylglycerol lipase, alpha gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20159446 1614089 Dagla diacylglycerol lipase, alpha gene MP:0003465 increased single cell response threshold IAGP N RGD:5509061 20141003 MGI PMID:21807615 1614089 Dagla diacylglycerol lipase, alpha gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:20159446 1614089 Dagla diacylglycerol lipase, alpha gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:21807615 1614089 Dagla diacylglycerol lipase, alpha gene MP:0003641 small lung IEA N RGD:5509061 20160811 MGI 1614089 Dagla diacylglycerol lipase, alpha gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160421 MGI 1614089 Dagla diacylglycerol lipase, alpha gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:20147530 1614089 Dagla diacylglycerol lipase, alpha gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:20147530 1614089 Dagla diacylglycerol lipase, alpha gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1614090 Gpr152 G protein-coupled receptor 152 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1614090 Gpr152 G protein-coupled receptor 152 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20170105 MGI 1614090 Gpr152 G protein-coupled receptor 152 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160421 MGI 1614097 Or5b112 olfactory receptor family 5 subfamily B member 112 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1614123 Rragb Ras-related GTP binding B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20181122 MGI PMID:24768164 1614127 Tbc1d8b TBC1 domain family, member 8B gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220519 MGI 1614128 Fam199x family with sequence similarity 199, X-linked gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1614128 Fam199x family with sequence similarity 199, X-linked gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210128 MGI 1614128 Fam199x family with sequence similarity 199, X-linked gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1614130 Nxf3 nuclear RNA export factor 3 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23677977 1614130 Nxf3 nuclear RNA export factor 3 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23677977 1614130 Nxf3 nuclear RNA export factor 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23677977 1614130 Nxf3 nuclear RNA export factor 3 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23677977 1614130 Nxf3 nuclear RNA export factor 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21308854 1614130 Nxf3 nuclear RNA export factor 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23677977 1614130 Nxf3 nuclear RNA export factor 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21308854 1614130 Nxf3 nuclear RNA export factor 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23677977 1614130 Nxf3 nuclear RNA export factor 3 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23677977 1614130 Nxf3 nuclear RNA export factor 3 gene MP:0009240 elongated sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:23677977 1614130 Nxf3 nuclear RNA export factor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23677977 1614130 Nxf3 nuclear RNA export factor 3 gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23677977 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20190502 MGI PMID:30926797 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20190502 MGI PMID:30926797 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20190502 MGI PMID:30926797 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20190502 MGI PMID:30926797 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20190502 MGI PMID:30926797 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20190502 MGI PMID:30926797 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20190502 MGI PMID:30926797 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20190502 MGI PMID:30926797 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20190502 MGI PMID:30926797 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20190502 MGI PMID:30926797 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20190502 MGI PMID:30926797 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20190502 MGI PMID:30926797 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20190502 MGI PMID:30926797 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20190502 MGI PMID:30926797 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20190502 MGI PMID:30926797 1614131 Gprasp2 G protein-coupled receptor associated sorting protein 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:30926797 1614133 Defb14 defensin beta 14 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20160421 MGI 1614133 Defb14 defensin beta 14 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 1614133 Defb14 defensin beta 14 gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20210128 MGI 1614133 Defb14 defensin beta 14 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1614133 Defb14 defensin beta 14 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1614136 Kcng1 potassium voltage-gated channel, subfamily G, member 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1614136 Kcng1 potassium voltage-gated channel, subfamily G, member 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1614136 Kcng1 potassium voltage-gated channel, subfamily G, member 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1614136 Kcng1 potassium voltage-gated channel, subfamily G, member 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1614136 Kcng1 potassium voltage-gated channel, subfamily G, member 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1614139 Dipk1c divergent protein kinase domain 1C gene MP:0001399 hyperactivity IAGP N RGD:5509061 20230713 MGI PMID:35858575 1614139 Dipk1c divergent protein kinase domain 1C gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1614139 Dipk1c divergent protein kinase domain 1C gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20230713 MGI PMID:35858575 1614139 Dipk1c divergent protein kinase domain 1C gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20230713 MGI PMID:35858575 1614139 Dipk1c divergent protein kinase domain 1C gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20230713 MGI PMID:35858575 1614139 Dipk1c divergent protein kinase domain 1C gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:35858575 1614139 Dipk1c divergent protein kinase domain 1C gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20230713 MGI PMID:35858575 1614140 Kcng2 potassium voltage-gated channel, subfamily G, member 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1614140 Kcng2 potassium voltage-gated channel, subfamily G, member 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 1614140 Kcng2 potassium voltage-gated channel, subfamily G, member 2 gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20221215 MGI 1614140 Kcng2 potassium voltage-gated channel, subfamily G, member 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210520 MGI 1614140 Kcng2 potassium voltage-gated channel, subfamily G, member 2 gene MP:0011952 decreased cardiac stroke volume IEA N RGD:5509061 20190502 MGI 1614141 Loxhd1 lipoxygenase homology domains 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17329413 1614141 Loxhd1 lipoxygenase homology domains 1 gene MP:0001967 deafness IAGP N RGD:5509061 20160929 MGI PMID:27534441 1614141 Loxhd1 lipoxygenase homology domains 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19732867 1614141 Loxhd1 lipoxygenase homology domains 1 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:19732867 1614141 Loxhd1 lipoxygenase homology domains 1 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19732867 1614141 Loxhd1 lipoxygenase homology domains 1 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:19732867 1614141 Loxhd1 lipoxygenase homology domains 1 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:19732867 1614141 Loxhd1 lipoxygenase homology domains 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17329413 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20210429 MGI PMID:32289885 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20210429 MGI PMID:31862898 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220519 MGI 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0000274 enlarged heart IEA N RGD:5509061 20220519 MGI 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20210429 MGI PMID:31862898 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220519 MGI 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220519 MGI 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0001860 liver inflammation IAGP N RGD:5509061 20210429 MGI PMID:32289885 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20210429 MGI PMID:32289885 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20210429 MGI PMID:32289885 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0002981 increased liver weight IAGP N RGD:5509061 20210429 MGI PMID:32289885 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20210429 MGI PMID:31862898 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20210429 MGI PMID:32289885 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20210429 MGI PMID:32289885 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20210429 MGI PMID:32289885 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20210429 MGI PMID:31862898 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20210429 MGI PMID:31862898 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20210429 MGI PMID:32289885 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20210429 MGI PMID:32289885 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20210429 MGI PMID:32289885 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20210429 MGI PMID:32289885 1614142 Fhip2b FHF complex subunit HOOK interacting protein 2B gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20210429 MGI PMID:31862898 1614144 Nuggc nuclear GTPase, germinal center associated gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1614144 Nuggc nuclear GTPase, germinal center associated gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1614144 Nuggc nuclear GTPase, germinal center associated gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1614144 Nuggc nuclear GTPase, germinal center associated gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1614144 Nuggc nuclear GTPase, germinal center associated gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1614144 Nuggc nuclear GTPase, germinal center associated gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230119 MGI 1614144 Nuggc nuclear GTPase, germinal center associated gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230119 MGI 1614144 Nuggc nuclear GTPase, germinal center associated gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1614144 Nuggc nuclear GTPase, germinal center associated gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 1614144 Nuggc nuclear GTPase, germinal center associated gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:22833677 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0001260 increased body weight IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0001261 obese IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614146 C1qtnf9 C1q and tumor necrosis factor related protein 9 gene MP:0011939 increased food intake IAGP N RGD:5509061 20151210 MGI PMID:24473438 1614147 Setdb2 SET domain, bifurcated 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20160324 MGI PMID:25419628 1614147 Setdb2 SET domain, bifurcated 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20160804 MGI 1614147 Setdb2 SET domain, bifurcated 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20160324 MGI PMID:25419628 1614147 Setdb2 SET domain, bifurcated 2 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20160804 MGI 1614147 Setdb2 SET domain, bifurcated 2 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20160324 MGI PMID:25419628 1614147 Setdb2 SET domain, bifurcated 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20160804 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0000106 abnormal basisphenoid bone morphology IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0000141 abnormal vertebral body morphology IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0000614 absent salivary gland IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20190829 MGI PMID:30665704 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0000897 abnormal midbrain morphology IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0000928 incomplete rostral neuropore closure IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0000963 fused dorsal root ganglion IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20190829 MGI PMID:30665704 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20190829 MGI PMID:30665704 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0002240 abnormal paranasal sinus morphology IAGP N RGD:5509061 20190829 MGI PMID:30665704 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20190829 MGI PMID:30665704 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0002767 situs ambiguus IAGP N RGD:5509061 20190829 MGI PMID:30665704 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0003078 aphakia IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0003266 biliary cyst IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0003330 abnormal auditory tube morphology IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0003586 dilated ureter IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0004603 absent vertebral arch IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0004666 absent stapedial artery IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0005587 abnormal Meckel's cartilage morphology IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20181227 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0009576 oral atresia IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0009905 absent tongue IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20190829 MGI PMID:30665704 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20190829 MGI PMID:30665704 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0013820 absent optic cup IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0013823 absent segment of anterior cerebral artery IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0013852 abnormal Mullerian duct topology IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0013875 increased trigeminal neuroma incidence IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0013936 abnormal thymus topology IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0013976 abnormal left vena cava superior connection IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0013995 abnormal external carotid artery origin IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0014018 embryo tumor IEA N RGD:5509061 20170504 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0020488 abnormal middle cerebral artery origin IEA N RGD:5509061 20180628 MGI 1614148 Gas2l2 growth arrest-specific 2 like 2 gene MP:0020490 abnormal ophthalmic artery origin IEA N RGD:5509061 20180628 MGI 1614149 Slfn14 schlafen 14 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230119 MGI 1614149 Slfn14 schlafen 14 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20220630 MGI PMID:33496736 1614149 Slfn14 schlafen 14 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20220630 MGI PMID:33496736 1614149 Slfn14 schlafen 14 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20220630 MGI PMID:33496736 1614149 Slfn14 schlafen 14 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20230119 MGI 1614149 Slfn14 schlafen 14 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20220630 MGI PMID:33496736 1614149 Slfn14 schlafen 14 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230119 MGI 1614149 Slfn14 schlafen 14 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1614149 Slfn14 schlafen 14 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20220630 MGI PMID:33496736 1614149 Slfn14 schlafen 14 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20220630 MGI PMID:33496736 1614149 Slfn14 schlafen 14 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1614149 Slfn14 schlafen 14 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20220630 MGI PMID:33496736 1614149 Slfn14 schlafen 14 gene MP:0002813 microcytosis IAGP N RGD:5509061 20220630 MGI PMID:33496736 1614149 Slfn14 schlafen 14 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20220630 MGI PMID:33496736 1614149 Slfn14 schlafen 14 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20220630 MGI PMID:33496736 1614149 Slfn14 schlafen 14 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20220630 MGI PMID:33496736 1614149 Slfn14 schlafen 14 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20220630 MGI PMID:33496736 1614149 Slfn14 schlafen 14 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20220630 MGI PMID:33496736 1614149 Slfn14 schlafen 14 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1614149 Slfn14 schlafen 14 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1614149 Slfn14 schlafen 14 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230119 MGI 1614149 Slfn14 schlafen 14 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20220630 MGI PMID:33496736 1614149 Slfn14 schlafen 14 gene MP:0013704 increased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20220630 MGI PMID:33496736 1614151 Slfn9 schlafen 9 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20240905 MGI PMID:38875319 1614151 Slfn9 schlafen 9 gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20240905 MGI PMID:38875319 1614153 Trarg1 trafficking regulator of GLUT4 (SLC2A4) 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:26629404 1614153 Trarg1 trafficking regulator of GLUT4 (SLC2A4) 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1614153 Trarg1 trafficking regulator of GLUT4 (SLC2A4) 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1614153 Trarg1 trafficking regulator of GLUT4 (SLC2A4) 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20200310 MGI PMID:26629404 1614153 Trarg1 trafficking regulator of GLUT4 (SLC2A4) 1 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:26629404 1614153 Trarg1 trafficking regulator of GLUT4 (SLC2A4) 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:26629404 1614153 Trarg1 trafficking regulator of GLUT4 (SLC2A4) 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200310 MGI PMID:26629404 1614153 Trarg1 trafficking regulator of GLUT4 (SLC2A4) 1 gene MP:0013277 abnormal fasting circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:26629404 1614153 Trarg1 trafficking regulator of GLUT4 (SLC2A4) 1 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20200310 MGI PMID:26629404 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0000097 short maxilla IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0000373 belly spot IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0000440 domed cranium IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20240523 MGI 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0000445 short snout IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20240523 MGI 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0001300 ocular hypertelorism IEA N RGD:5509061 20111116 MGI 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0005175 non-pigmented tail tip IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0006411 upturned snout IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0008188 abnormal transitional stage B cell morphology IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0008818 abnormal interfrontal bone morphology IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20200310 MGI 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0030444 premature cranial synchondrosis closure IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614154 Pfas phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) gene MP:0030466 alveolar process atrophy IAGP N RGD:5509061 20200310 MGI PMID:26234751 1614162 4933402N03Rik RIKEN cDNA 4933402N03 gene gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 1614162 4933402N03Rik RIKEN cDNA 4933402N03 gene gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20141003 MGI 1614162 4933402N03Rik RIKEN cDNA 4933402N03 gene gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20201022 MGI 1614162 4933402N03Rik RIKEN cDNA 4933402N03 gene gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1614162 4933402N03Rik RIKEN cDNA 4933402N03 gene gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1614164 Cpa2 carboxypeptidase A2, pancreatic gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20220811 MGI 1614164 Cpa2 carboxypeptidase A2, pancreatic gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1614164 Cpa2 carboxypeptidase A2, pancreatic gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 1614165 Ccdc136 coiled-coil domain containing 136 gene MP:0001925 male infertility IAGP N RGD:5509061 20180705 MGI PMID:27076447 1614165 Ccdc136 coiled-coil domain containing 136 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20180705 MGI PMID:27076447 1614165 Ccdc136 coiled-coil domain containing 136 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20180705 MGI PMID:27076447 1614165 Ccdc136 coiled-coil domain containing 136 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20180705 MGI PMID:27076447 1614165 Ccdc136 coiled-coil domain containing 136 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20180705 MGI PMID:27076447 1614165 Ccdc136 coiled-coil domain containing 136 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20180705 MGI PMID:27076447 1614167 Phf24 PHD finger protein 24 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20160225 MGI PMID:25242222 1614167 Phf24 PHD finger protein 24 gene MP:0002735 abnormal chemical nociception IAGP N RGD:5509061 20160225 MGI PMID:25242222 1614167 Phf24 PHD finger protein 24 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20160225 MGI PMID:25242222 1614170 Xkr7 X-linked Kx blood group related 7 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1614170 Xkr7 X-linked Kx blood group related 7 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1614170 Xkr7 X-linked Kx blood group related 7 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1614171 6820408C15Rik RIKEN cDNA 6820408C15 gene gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20240523 MGI 1614171 6820408C15Rik RIKEN cDNA 6820408C15 gene gene MP:0009476 enlarged cecum IEA N RGD:5509061 20240523 MGI 1614172 Nrsn2 neurensin 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20230601 MGI 1614172 Nrsn2 neurensin 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20231207 MGI 1614172 Nrsn2 neurensin 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20230601 MGI 1614172 Nrsn2 neurensin 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20231207 MGI 1614172 Nrsn2 neurensin 2 gene MP:0008821 increased blood uric acid level IEA N RGD:5509061 20230601 MGI 1614172 Nrsn2 neurensin 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0000745 tremors IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0004142 abnormal muscle tone IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0009979 abnormal cerebellum deep nucleus morphology IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0012051 spasticity IAGP N RGD:5509061 20220106 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:31754024 1614173 Psmf1 proteasome (prosome, macropain) inhibitor subunit 1 gene MP:0014330 abnormal Purkinje cell focal axonal swelling IAGP N RGD:5509061 20240118 MGI PMID:31754024 1614175 Kiz kizuna centrosomal protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18423593 1614177 Cdh19 cadherin 19, type 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 1614177 Cdh19 cadherin 19, type 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1614183 Usp49 ubiquitin specific peptidase 49 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20200423 MGI PMID:30943264 1614183 Usp49 ubiquitin specific peptidase 49 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20200423 MGI PMID:30943264 1614183 Usp49 ubiquitin specific peptidase 49 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20200423 MGI PMID:30943264 1614183 Usp49 ubiquitin specific peptidase 49 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20200423 MGI PMID:30943264 1614183 Usp49 ubiquitin specific peptidase 49 gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:30943264 1614183 Usp49 ubiquitin specific peptidase 49 gene MP:0031025 decreased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:30943264 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20181227 MGI 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14585983 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:14585983 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14585983 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:14585983 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:14585983 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:14585983 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:14585983 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:14585983 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:14585983 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14585983 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:16606826 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:14585983 1614185 Ubr2 ubiquitin protein ligase E3 component n-recognin 2 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20150312 MGI PMID:14585983 1614187 Eny2 ENY2 transcription and export complex 2 subunit gene MP:0001714 absent trophoblast giant cells IEA N RGD:5509061 20241010 MGI 1614187 Eny2 ENY2 transcription and export complex 2 subunit gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241010 MGI 1614187 Eny2 ENY2 transcription and export complex 2 subunit gene MP:0004964 absent inner cell mass IEA N RGD:5509061 20241010 MGI 1614187 Eny2 ENY2 transcription and export complex 2 subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1614187 Eny2 ENY2 transcription and export complex 2 subunit gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241010 MGI 1614188 Zfp595 zinc finger protein 595 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1614188 Zfp595 zinc finger protein 595 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20210128 MGI 1614188 Zfp595 zinc finger protein 595 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1614188 Zfp595 zinc finger protein 595 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1614189 Prss47 serine protease 47 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1614189 Prss47 serine protease 47 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220519 MGI 1614189 Prss47 serine protease 47 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220519 MGI 1614189 Prss47 serine protease 47 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220519 MGI 1614189 Prss47 serine protease 47 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220519 MGI 1614189 Prss47 serine protease 47 gene MP:0001147 small testis IEA N RGD:5509061 20220519 MGI 1614189 Prss47 serine protease 47 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20220519 MGI 1614189 Prss47 serine protease 47 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20220519 MGI 1614189 Prss47 serine protease 47 gene MP:0009709 hydrometra IEA N RGD:5509061 20220519 MGI 1614189 Prss47 serine protease 47 gene MP:0013129 abnormal tooth color IEA N RGD:5509061 20220519 MGI 1614190 Hlf hepatic leukemia factor gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180705 MGI PMID:16814730 1614190 Hlf hepatic leukemia factor gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:15175240 1614190 Hlf hepatic leukemia factor gene MP:0001596 hypotension IAGP N RGD:5509061 20180705 MGI PMID:20686175 1614190 Hlf hepatic leukemia factor gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20180705 MGI PMID:20686175 1614190 Hlf hepatic leukemia factor gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15175240 1614190 Hlf hepatic leukemia factor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15175240 1614190 Hlf hepatic leukemia factor gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15175240 1614190 Hlf hepatic leukemia factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180705 MGI PMID:15175240 1614190 Hlf hepatic leukemia factor gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20180705 MGI PMID:20686175 1614190 Hlf hepatic leukemia factor gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180705 MGI PMID:16814730 1614190 Hlf hepatic leukemia factor gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:15175240 1614190 Hlf hepatic leukemia factor gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:15175240 1614190 Hlf hepatic leukemia factor gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:15175240 1614190 Hlf hepatic leukemia factor gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20180920 MGI PMID:15175240 1614190 Hlf hepatic leukemia factor gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180705 MGI PMID:16814730 1614190 Hlf hepatic leukemia factor gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20180705 MGI PMID:16814730 1614190 Hlf hepatic leukemia factor gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:15175240 1614192 Trim25 tripartite motif-containing 25 gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:10518570 1614192 Trim25 tripartite motif-containing 25 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180426 MGI PMID:27721430 1614192 Trim25 tripartite motif-containing 25 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20180426 MGI PMID:27721430 1614192 Trim25 tripartite motif-containing 25 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1614192 Trim25 tripartite motif-containing 25 gene MP:0010751 decreased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20180426 MGI PMID:27721430 1614193 Elobl elongin B-like gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38786026 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0001147 small testis IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:28592902 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200310 MGI 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20200310 MGI PMID:26764350 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:28592902 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:28592902 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220519 MGI 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0003717 pallor IAGP N RGD:5509061 20200310 MGI PMID:26764350 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0004266 pale placenta IAGP N RGD:5509061 20200310 MGI PMID:26764350 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0004930 small epididymis IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:28592902 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20200310 MGI PMID:28592902 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:28592902 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:26764350 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0008957 abnormal placenta junctional zone morphology IAGP N RGD:5509061 20200310 MGI PMID:26764350 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20211021 MGI 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:26764350 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28592902 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20200310 MGI 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:28592902 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20200310 MGI PMID:28592902 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614194 Ggnbp2 gametogenetin binding protein 2 gene MP:0031374 abnormal manchette assembly IAGP N RGD:5509061 20220407 MGI PMID:28823874 1614196 Adgb androglobin gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1614196 Adgb androglobin gene MP:0001891 hydrocephaly IEA N RGD:5509061 20210128 MGI 1614196 Adgb androglobin gene MP:0001925 male infertility IAGP N RGD:5509061 20220721 MGI PMID:35700329 1614196 Adgb androglobin gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1614196 Adgb androglobin gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1614196 Adgb androglobin gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210128 MGI 1614196 Adgb androglobin gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220721 MGI PMID:35700329 1614196 Adgb androglobin gene MP:0004818 increased skeletal muscle mass IEA N RGD:5509061 20210520 MGI 1614196 Adgb androglobin gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220721 MGI PMID:35700329 1614196 Adgb androglobin gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20210128 MGI 1614196 Adgb androglobin gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220721 MGI PMID:35700329 1614196 Adgb androglobin gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220721 MGI PMID:35700329 1614196 Adgb androglobin gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220721 MGI PMID:35700329 1614196 Adgb androglobin gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220721 MGI PMID:35700329 1614196 Adgb androglobin gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1614196 Adgb androglobin gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220721 MGI PMID:35700329 1614196 Adgb androglobin gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20200310 MGI PMID:28288139 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20200310 MGI PMID:28288139 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0000601 small liver IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0000618 small salivary gland IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0000692 small spleen IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:28288139 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0002164 abnormal gland physiology IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0002188 small heart IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0002691 small stomach IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20200310 MGI PMID:28288139 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0002989 small kidney IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0003432 increased activity of parathyroid IAGP N RGD:5509061 20200310 MGI PMID:28288139 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0003495 increased parathyroid adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:28288139 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0003641 small lung IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0003946 renal necrosis IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0005324 ascites IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20200310 MGI PMID:28288139 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0009082 uterus cyst IAGP N RGD:5509061 20200310 MGI PMID:28288139 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:28288139 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0009222 increased uterus tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:28288139 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0010321 increased parathyroid gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:28288139 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0012118 absent trophectoderm cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614198 Cdc73 cell division cycle 73, Paf1/RNA polymerase II complex component gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20200310 MGI PMID:18212049 1614206 Tmem151b transmembrane protein 151B gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 1614206 Tmem151b transmembrane protein 151B gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1614206 Tmem151b transmembrane protein 151B gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20230601 MGI 1614206 Tmem151b transmembrane protein 151B gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20170105 MGI 1614206 Tmem151b transmembrane protein 151B gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1614211 Csta1 cystatin A1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20231207 MGI PMID:37118283 1614211 Csta1 cystatin A1 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20231207 MGI PMID:37118283 1614211 Csta1 cystatin A1 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20231207 MGI PMID:37118283 1614211 Csta1 cystatin A1 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20231207 MGI PMID:37118283 1614211 Csta1 cystatin A1 gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20231207 MGI PMID:37118283 1614211 Csta1 cystatin A1 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20231207 MGI PMID:37118283 1614211 Csta1 cystatin A1 gene MP:0010962 decreased compact bone mass IAGP N RGD:5509061 20231207 MGI PMID:37118283 1614212 Vcpkmt valosin containing protein lysine (K) methyltransferase gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 1614212 Vcpkmt valosin containing protein lysine (K) methyltransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180301 MGI PMID:26544960 1614212 Vcpkmt valosin containing protein lysine (K) methyltransferase gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1614212 Vcpkmt valosin containing protein lysine (K) methyltransferase gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20220519 MGI 1614212 Vcpkmt valosin containing protein lysine (K) methyltransferase gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220519 MGI 1614212 Vcpkmt valosin containing protein lysine (K) methyltransferase gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1614213 Alg11 ALG11 alpha-1,2-mannosyltransferase gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1614213 Alg11 ALG11 alpha-1,2-mannosyltransferase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1614213 Alg11 ALG11 alpha-1,2-mannosyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614213 Alg11 ALG11 alpha-1,2-mannosyltransferase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1614214 Urb1 URB1 ribosome biogenesis 1 homolog (S. cerevisiae) gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20240523 MGI 1614214 Urb1 URB1 ribosome biogenesis 1 homolog (S. cerevisiae) gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20240704 MGI PMID:36890225 1614214 Urb1 URB1 ribosome biogenesis 1 homolog (S. cerevisiae) gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20240704 MGI PMID:36890225 1614214 Urb1 URB1 ribosome biogenesis 1 homolog (S. cerevisiae) gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20220811 MGI 1614214 Urb1 URB1 ribosome biogenesis 1 homolog (S. cerevisiae) gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20240704 MGI PMID:36890225 1614214 Urb1 URB1 ribosome biogenesis 1 homolog (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614214 Urb1 URB1 ribosome biogenesis 1 homolog (S. cerevisiae) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1614216 Sun3 Sad1 and UNC84 domain containing 3 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20240523 MGI 1614216 Sun3 Sad1 and UNC84 domain containing 3 gene MP:0001147 small testis IAGP N RGD:5509061 20210506 MGI PMID:32156700 1614216 Sun3 Sad1 and UNC84 domain containing 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20210506 MGI PMID:32156700 1614216 Sun3 Sad1 and UNC84 domain containing 3 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20210506 MGI PMID:32156700 1614216 Sun3 Sad1 and UNC84 domain containing 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210506 MGI PMID:32156700 1614216 Sun3 Sad1 and UNC84 domain containing 3 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20210506 MGI PMID:32156700 1614216 Sun3 Sad1 and UNC84 domain containing 3 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20210506 MGI PMID:32156700 1614216 Sun3 Sad1 and UNC84 domain containing 3 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20210506 MGI PMID:32156700 1614217 Mical1 microtubule associated monooxygenase, calponin and LIM domain containing 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20240523 MGI PMID:25007825 1614217 Mical1 microtubule associated monooxygenase, calponin and LIM domain containing 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20240523 MGI PMID:25007825 1614217 Mical1 microtubule associated monooxygenase, calponin and LIM domain containing 1 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20240523 MGI PMID:25007825 1614217 Mical1 microtubule associated monooxygenase, calponin and LIM domain containing 1 gene MP:0004085 abnormal heartbeat IAGP N RGD:5509061 20240523 MGI PMID:32749237 1614217 Mical1 microtubule associated monooxygenase, calponin and LIM domain containing 1 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20240523 MGI PMID:25007825 1614217 Mical1 microtubule associated monooxygenase, calponin and LIM domain containing 1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20240523 MGI PMID:25007825 1614217 Mical1 microtubule associated monooxygenase, calponin and LIM domain containing 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20240523 MGI PMID:25007825 1614217 Mical1 microtubule associated monooxygenase, calponin and LIM domain containing 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20240523 MGI PMID:32749237 1614218 Ucn2 urocortin 2 gene MP:0001422 abnormal drinking behavior IAGP N RGD:5509061 20141003 MGI PMID:16707802 1614218 Ucn2 urocortin 2 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:16707802 1614218 Ucn2 urocortin 2 gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:16707802 1614218 Ucn2 urocortin 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16707802 1614218 Ucn2 urocortin 2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:16707802 1614227 Chd9 chromodomain helicase DNA binding protein 9 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:29665362 1614227 Chd9 chromodomain helicase DNA binding protein 9 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1614227 Chd9 chromodomain helicase DNA binding protein 9 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20201022 MGI 1614227 Chd9 chromodomain helicase DNA binding protein 9 gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20200310 MGI 1614227 Chd9 chromodomain helicase DNA binding protein 9 gene MP:0013412 increased Langerhans cell number IEA N RGD:5509061 20201231 MGI 1614230 Nsd2 nuclear receptor binding SET domain protein 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19483677 1614230 Nsd2 nuclear receptor binding SET domain protein 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:19483677 1614230 Nsd2 nuclear receptor binding SET domain protein 2 gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20141003 MGI PMID:19483677 1614230 Nsd2 nuclear receptor binding SET domain protein 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19483677 1614230 Nsd2 nuclear receptor binding SET domain protein 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:19483677 1614230 Nsd2 nuclear receptor binding SET domain protein 2 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:19483677 1614230 Nsd2 nuclear receptor binding SET domain protein 2 gene MP:0008278 failure of sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:19483677 1614230 Nsd2 nuclear receptor binding SET domain protein 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:19483677 1614230 Nsd2 nuclear receptor binding SET domain protein 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19483677 1614230 Nsd2 nuclear receptor binding SET domain protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19483677 1614230 Nsd2 nuclear receptor binding SET domain protein 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19483677 1614231 Scml2 Scm polycomb group protein like 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210520 MGI 1614231 Scml2 Scm polycomb group protein like 2 gene MP:0001147 small testis IAGP N RGD:5509061 20151112 MGI PMID:25703348 1614231 Scml2 Scm polycomb group protein like 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20151112 MGI PMID:25703348 1614231 Scml2 Scm polycomb group protein like 2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20151112 MGI PMID:25703348 1614231 Scml2 Scm polycomb group protein like 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20151112 MGI PMID:25703348 1614231 Scml2 Scm polycomb group protein like 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:25703348 1614231 Scml2 Scm polycomb group protein like 2 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220623 MGI PMID:25703348 1614233 Gpsm3 G-protein signalling modulator 3 (AGS3-like, C. elegans) gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20231207 MGI 1614233 Gpsm3 G-protein signalling modulator 3 (AGS3-like, C. elegans) gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23280397 1614233 Gpsm3 G-protein signalling modulator 3 (AGS3-like, C. elegans) gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23280397 1614233 Gpsm3 G-protein signalling modulator 3 (AGS3-like, C. elegans) gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:23280397 1614233 Gpsm3 G-protein signalling modulator 3 (AGS3-like, C. elegans) gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:23280397 1614234 Tasor2 transcription activation suppressor family member 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1614234 Tasor2 transcription activation suppressor family member 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1614234 Tasor2 transcription activation suppressor family member 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220519 MGI 1614234 Tasor2 transcription activation suppressor family member 2 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1614236 Oaf out at first homolog gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1614238 Brk1 BRICK1, SCAR/WAVE actin-nucleating complex subunit gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:20861187 1614238 Brk1 BRICK1, SCAR/WAVE actin-nucleating complex subunit gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:20861187 1614238 Brk1 BRICK1, SCAR/WAVE actin-nucleating complex subunit gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20861187 1614238 Brk1 BRICK1, SCAR/WAVE actin-nucleating complex subunit gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:20861187 1614238 Brk1 BRICK1, SCAR/WAVE actin-nucleating complex subunit gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:20861187 1614238 Brk1 BRICK1, SCAR/WAVE actin-nucleating complex subunit gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20861187 1614238 Brk1 BRICK1, SCAR/WAVE actin-nucleating complex subunit gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20230615 MGI PMID:20861187 1614239 Rcc1 regulator of chromosome condensation 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1614239 Rcc1 regulator of chromosome condensation 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1614240 Kti12 KTI12 homolog, chromatin associated gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1614240 Kti12 KTI12 homolog, chromatin associated gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1614240 Kti12 KTI12 homolog, chromatin associated gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1614240 Kti12 KTI12 homolog, chromatin associated gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1614240 Kti12 KTI12 homolog, chromatin associated gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614240 Kti12 KTI12 homolog, chromatin associated gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1614242 Lrrc19 leucine rich repeat containing 19 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20190509 MGI PMID:25026888 1614242 Lrrc19 leucine rich repeat containing 19 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20190509 MGI PMID:25026888 1614242 Lrrc19 leucine rich repeat containing 19 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20190509 MGI PMID:25026888 1614243 Ldlrap1 low density lipoprotein receptor adaptor protein 1 gene MP:0000181 abnormal circulating LDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:12746448 1614243 Ldlrap1 low density lipoprotein receptor adaptor protein 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:12746448 1614243 Ldlrap1 low density lipoprotein receptor adaptor protein 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:15472122 1614243 Ldlrap1 low density lipoprotein receptor adaptor protein 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:12746448 1614243 Ldlrap1 low density lipoprotein receptor adaptor protein 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:12746448 1614243 Ldlrap1 low density lipoprotein receptor adaptor protein 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:15472122 1614245 Kcnb2 potassium voltage gated channel, Shab-related subfamily, member 2 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20221215 MGI 1614245 Kcnb2 potassium voltage gated channel, Shab-related subfamily, member 2 gene MP:0000746 weakness IEA N RGD:5509061 20141003 MGI 1614245 Kcnb2 potassium voltage gated channel, Shab-related subfamily, member 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1614245 Kcnb2 potassium voltage gated channel, Shab-related subfamily, member 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20141003 MGI 1614245 Kcnb2 potassium voltage gated channel, Shab-related subfamily, member 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20141003 MGI 1614245 Kcnb2 potassium voltage gated channel, Shab-related subfamily, member 2 gene MP:0001501 abnormal sleep pattern IEA N RGD:5509061 20141003 MGI 1614245 Kcnb2 potassium voltage gated channel, Shab-related subfamily, member 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20221215 MGI 1614245 Kcnb2 potassium voltage gated channel, Shab-related subfamily, member 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1614245 Kcnb2 potassium voltage gated channel, Shab-related subfamily, member 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1614249 Tnxb tenascin XB gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1614249 Tnxb tenascin XB gene MP:0000691 enlarged spleen IEA N RGD:5509061 20170105 MGI 1614249 Tnxb tenascin XB gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:11737270 1614249 Tnxb tenascin XB gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1614249 Tnxb tenascin XB gene MP:0005275 abnormal skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:11925569 1614249 Tnxb tenascin XB gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1614249 Tnxb tenascin XB gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:15242785 1614249 Tnxb tenascin XB gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11737270 1614249 Tnxb tenascin XB gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230601 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20200310 MGI PMID:24990152 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20200310 MGI PMID:24990152 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200310 MGI PMID:25625206 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20200310 MGI PMID:14993192 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20200310 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20200310 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0001333 absent optic nerve IEA N RGD:5509061 20210128 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20200310 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20200310 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200310 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20200310 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20200310 MGI PMID:14993192 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0001706 abnormal left-right axis patterning IEA N RGD:5509061 20200310 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20200310 MGI PMID:14993192 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0001726 abnormal allantois morphology IEA N RGD:5509061 20200310 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:14993192 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:24990152 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:27027284 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20200310 MGI PMID:24990152 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20200310 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20200310 MGI PMID:25625206 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20200310 MGI PMID:14993192 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200310 MGI PMID:25625206 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20200310 MGI PMID:24990152 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:21859843 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:24990152 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0002824 abnormal chorioallantoic fusion IEA N RGD:5509061 20200310 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20200310 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20200310 MGI PMID:25625206 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20200310 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20200310 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20200310 MGI PMID:24990152 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0004125 abnormal venule morphology IAGP N RGD:5509061 20200310 MGI PMID:27027284 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0004175 telangiectasia IAGP N RGD:5509061 20200310 MGI PMID:24990152 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20200310 MGI PMID:14993192 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20200310 MGI PMID:14993192 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:21859843 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:24990152 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:27027284 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:27513872 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0006182 increased retina hemangioma incidence IAGP N RGD:5509061 20200310 MGI PMID:24990152 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20200310 MGI PMID:25625206 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0009806 abnormal otic vesicle morphology IEA N RGD:5509061 20200310 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0010574 dilated aorta IAGP N RGD:5509061 20200310 MGI PMID:14993192 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0010662 abnormal intersomitic artery morphology IAGP N RGD:5509061 20200310 MGI PMID:14993192 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:14993192 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20668652 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24990152 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25625206 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0012495 pharyngeal arch artery stenosis IAGP N RGD:5509061 20200310 MGI PMID:14993192 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0013146 eye lesions IAGP N RGD:5509061 20200310 MGI PMID:24990152 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220519 MGI 1614252 Krit1 KRIT1, ankyrin repeat containing gene MP:0031593 decreased cardiac jelly amount IAGP N RGD:5509061 20240229 MGI PMID:25625206 1614254 Hdac9 histone deacetylase 9 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15367668 1614254 Hdac9 histone deacetylase 9 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12202037 1614254 Hdac9 histone deacetylase 9 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15367668 1614254 Hdac9 histone deacetylase 9 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15367668 1614254 Hdac9 histone deacetylase 9 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15367668 1614254 Hdac9 histone deacetylase 9 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12202037 1614254 Hdac9 histone deacetylase 9 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12202037 1614254 Hdac9 histone deacetylase 9 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:17786239 1614254 Hdac9 histone deacetylase 9 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15367668 1614254 Hdac9 histone deacetylase 9 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15367668 1614261 Krtap17-1 keratin associated protein 17-1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1614261 Krtap17-1 keratin associated protein 17-1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1614261 Krtap17-1 keratin associated protein 17-1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1614261 Krtap17-1 keratin associated protein 17-1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1614261 Krtap17-1 keratin associated protein 17-1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20160421 MGI 1614261 Krtap17-1 keratin associated protein 17-1 gene MP:0001192 scaly skin IEA N RGD:5509061 20210520 MGI 1614261 Krtap17-1 keratin associated protein 17-1 gene MP:0001200 thick skin IEA N RGD:5509061 20210520 MGI 1614261 Krtap17-1 keratin associated protein 17-1 gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 1614261 Krtap17-1 keratin associated protein 17-1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20181227 MGI 1614261 Krtap17-1 keratin associated protein 17-1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20160421 MGI 1614261 Krtap17-1 keratin associated protein 17-1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1614261 Krtap17-1 keratin associated protein 17-1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 1614261 Krtap17-1 keratin associated protein 17-1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1614261 Krtap17-1 keratin associated protein 17-1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20181227 MGI 1614261 Krtap17-1 keratin associated protein 17-1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1614270 Srxn1 sulfiredoxin 1 homolog (S. cerevisiae) gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20200310 MGI PMID:22681886 1614270 Srxn1 sulfiredoxin 1 homolog (S. cerevisiae) gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20200310 MGI PMID:22681886 1614270 Srxn1 sulfiredoxin 1 homolog (S. cerevisiae) gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:21083423 1614270 Srxn1 sulfiredoxin 1 homolog (S. cerevisiae) gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200310 MGI PMID:21083423 1614270 Srxn1 sulfiredoxin 1 homolog (S. cerevisiae) gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20200310 MGI PMID:22681886 1614270 Srxn1 sulfiredoxin 1 homolog (S. cerevisiae) gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20200310 MGI PMID:21083423 1614270 Srxn1 sulfiredoxin 1 homolog (S. cerevisiae) gene MP:0009078 adrenal gland hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:22681886 1614270 Srxn1 sulfiredoxin 1 homolog (S. cerevisiae) gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:21083423 1614271 Pkd1l2 polycystic kidney disease 1 like 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1614271 Pkd1l2 polycystic kidney disease 1 like 2 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1614271 Pkd1l2 polycystic kidney disease 1 like 2 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38786026 1614274 Lrmda leucine rich melanocyte differentiation associated gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1614274 Lrmda leucine rich melanocyte differentiation associated gene MP:0010052 increased grip strength IEA N RGD:5509061 20160114 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141030 MGI PMID:24395885 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220811 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0000601 small liver IEA N RGD:5509061 20220811 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220811 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141030 MGI PMID:24395885 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0000774 decreased brain size IEA N RGD:5509061 20220811 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20639863 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20231207 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20231207 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220519 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20231207 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20639863 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20221215 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20220811 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0002175 decreased brain weight IEA N RGD:5509061 20231207 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20231207 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0002989 small kidney IEA N RGD:5509061 20221215 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0003402 decreased liver weight IEA N RGD:5509061 20231207 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20639863 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20231207 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20639863 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141030 MGI PMID:24395885 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141030 MGI PMID:24395885 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20231207 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20231207 MGI 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0010132 decreased DN2 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0010134 decreased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141030 MGI PMID:24395885 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21613258 1614276 Msi2 musashi RNA-binding protein 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1614279 Llcfc1 LLLL and CFNLAS motif containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200716 MGI PMID:32393636 1614279 Llcfc1 LLLL and CFNLAS motif containing 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20231207 MGI 1614279 Llcfc1 LLLL and CFNLAS motif containing 1 gene MP:0031010 failure of sperm-egg fusion IAGP N RGD:5509061 20200716 MGI PMID:32393636 1614280 Sirt4 sirtuin 4 gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 1614280 Sirt4 sirtuin 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1614280 Sirt4 sirtuin 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16959573 1614280 Sirt4 sirtuin 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17923681 1614280 Sirt4 sirtuin 4 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20201022 MGI 1614280 Sirt4 sirtuin 4 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20160421 MGI 1614280 Sirt4 sirtuin 4 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20160421 MGI 1614291 4930563E22Rik RIKEN cDNA 4930563E22 gene gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20220519 MGI 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200310 MGI PMID:19270745 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20200310 MGI PMID:19270745 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:19270745 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:19270745 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19270745 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:19270745 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:19270745 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:19270745 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20200310 MGI PMID:19270745 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0004687 split vertebrae IAGP N RGD:5509061 20200310 MGI PMID:19270745 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20200310 MGI PMID:19270745 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20200310 MGI PMID:19270745 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20231207 MGI 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20231207 MGI 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19270745 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19270745 1614292 Asxl2 ASXL transcriptional regulator 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201022 MGI 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220811 MGI 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20210930 MGI PMID:32402064 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:19247432 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20210930 MGI PMID:32402064 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19247432 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0001147 small testis IAGP N RGD:5509061 20210930 MGI PMID:32402064 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20210930 MGI PMID:32402064 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20210930 MGI PMID:32402064 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20210826 MGI 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210520 MGI 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20181227 MGI 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0001924 infertility IAGP N RGD:5509061 20210930 MGI PMID:32402064 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19247432 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19247432 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:19247432 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20210930 MGI PMID:32402064 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20210520 MGI 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0002959 increased urine microalbumin level IEA N RGD:5509061 20211021 MGI 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20210930 MGI PMID:32402064 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:19247432 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20210930 MGI PMID:32402064 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20181227 MGI 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:19247432 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20210930 MGI PMID:32402064 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20210930 MGI PMID:32402064 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:19247432 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210826 MGI 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230601 MGI 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:19247432 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1614295 Syce1 synaptonemal complex central element protein 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:19247432 1614298 Vsir V-set immunoregulatory receptor gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20160602 MGI PMID:25964334 1614298 Vsir V-set immunoregulatory receptor gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20160602 MGI PMID:25964334 1614298 Vsir V-set immunoregulatory receptor gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20160602 MGI PMID:25964334 1614298 Vsir V-set immunoregulatory receptor gene MP:0002494 increased IgM level IAGP N RGD:5509061 20160602 MGI PMID:25964334 1614298 Vsir V-set immunoregulatory receptor gene MP:0002495 increased IgA level IAGP N RGD:5509061 20160602 MGI PMID:25964334 1614298 Vsir V-set immunoregulatory receptor gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20160602 MGI PMID:25964334 1614298 Vsir V-set immunoregulatory receptor gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20160602 MGI PMID:25964334 1614298 Vsir V-set immunoregulatory receptor gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20160602 MGI PMID:25964334 1614298 Vsir V-set immunoregulatory receptor gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20160602 MGI PMID:25964334 1614298 Vsir V-set immunoregulatory receptor gene MP:0009148 pancreas necrosis IAGP N RGD:5509061 20160602 MGI PMID:25964334 1614298 Vsir V-set immunoregulatory receptor gene MP:0010857 pulmonary necrosis IAGP N RGD:5509061 20160602 MGI PMID:25964334 1614299 Ddias DNA damage-induced apoptosis suppressor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20191219 MGI PMID:17515607 1614299 Ddias DNA damage-induced apoptosis suppressor gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20191219 MGI PMID:17515607 1614299 Ddias DNA damage-induced apoptosis suppressor gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20191219 MGI PMID:17515607 1614299 Ddias DNA damage-induced apoptosis suppressor gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20191219 MGI PMID:17515607 1614299 Ddias DNA damage-induced apoptosis suppressor gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20191219 MGI PMID:17515607 1614299 Ddias DNA damage-induced apoptosis suppressor gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20191219 MGI PMID:17515607 1614299 Ddias DNA damage-induced apoptosis suppressor gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20191219 MGI PMID:17515607 1614299 Ddias DNA damage-induced apoptosis suppressor gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20191219 MGI PMID:17515607 1614299 Ddias DNA damage-induced apoptosis suppressor gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20191219 MGI PMID:17515607 1614299 Ddias DNA damage-induced apoptosis suppressor gene MP:0014040 increased cellular sensitivity to DNA damaging agents IAGP N RGD:5509061 20191219 MGI PMID:17515607 1614300 Nol9 nucleolar protein 9 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1614300 Nol9 nucleolar protein 9 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1614300 Nol9 nucleolar protein 9 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230601 MGI 1614300 Nol9 nucleolar protein 9 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20230601 MGI 1614300 Nol9 nucleolar protein 9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614300 Nol9 nucleolar protein 9 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1614302 Msl1 male specific lethal 1 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20201231 MGI 1614302 Msl1 male specific lethal 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200514 MGI 1614303 Rd3 retinal degeneration 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1614303 Rd3 retinal degeneration 3 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:18344445 1614303 Rd3 retinal degeneration 3 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20231207 MGI 1614303 Rd3 retinal degeneration 3 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8486383 1614303 Rd3 retinal degeneration 3 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1614303 Rd3 retinal degeneration 3 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1614303 Rd3 retinal degeneration 3 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:8486383 1614303 Rd3 retinal degeneration 3 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20200402 MGI 1614303 Rd3 retinal degeneration 3 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:8486383 1614303 Rd3 retinal degeneration 3 gene MP:0008454 absent retina rod cells IAGP N RGD:5509061 20141003 MGI PMID:8486383 1614303 Rd3 retinal degeneration 3 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:8486383 1614303 Rd3 retinal degeneration 3 gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20240523 MGI 1614303 Rd3 retinal degeneration 3 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20211021 MGI 1614303 Rd3 retinal degeneration 3 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20221215 MGI 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20221215 MGI 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:21945076 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:21945076 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20221215 MGI 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20221215 MGI 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0001785 edema IEA N RGD:5509061 20221215 MGI 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21945076 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:21945076 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:21945076 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20221215 MGI 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:21945076 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21945076 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20220811 MGI 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0012270 cardiac edema IAGP N RGD:5509061 20141003 MGI PMID:21945076 1614304 Traf3ip1 TRAF3 interacting protein 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220811 MGI 1614305 Ttc19 tetratricopeptide repeat domain 19 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:30578322 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614307 Ndc1 NDC1 transmembrane nucleoporin gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:3220432 1614308 Fance Fanconi anemia, complementation group E gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20190926 MGI PMID:27486799 1614308 Fance Fanconi anemia, complementation group E gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20190926 MGI PMID:27486799 1614308 Fance Fanconi anemia, complementation group E gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20190926 MGI PMID:27486799 1614308 Fance Fanconi anemia, complementation group E gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20190926 MGI PMID:27486799 1614308 Fance Fanconi anemia, complementation group E gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20190926 MGI PMID:27486799 1614308 Fance Fanconi anemia, complementation group E gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20190926 MGI PMID:27486799 1614309 Arhgef10l Rho guanine nucleotide exchange factor 10-like gene MP:0003960 increased lean body mass IEA N RGD:5509061 20240523 MGI 1614310 Fam117b family with sequence similarity 117, member B gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20200310 MGI 1614310 Fam117b family with sequence similarity 117, member B gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20200310 MGI 1614310 Fam117b family with sequence similarity 117, member B gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20200310 MGI 1614310 Fam117b family with sequence similarity 117, member B gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20200310 MGI 1614310 Fam117b family with sequence similarity 117, member B gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200310 MGI 1614310 Fam117b family with sequence similarity 117, member B gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20200310 MGI 1614311 Tonsl tonsoku-like, DNA repair protein gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200220 MGI PMID:30773278 1614311 Tonsl tonsoku-like, DNA repair protein gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20200220 MGI PMID:30773278 1614311 Tonsl tonsoku-like, DNA repair protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200220 MGI PMID:30773278 1614311 Tonsl tonsoku-like, DNA repair protein gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 1614311 Tonsl tonsoku-like, DNA repair protein gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20220519 MGI 1614311 Tonsl tonsoku-like, DNA repair protein gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200220 MGI PMID:30773278 1614311 Tonsl tonsoku-like, DNA repair protein gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20220519 MGI 1614311 Tonsl tonsoku-like, DNA repair protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200220 MGI PMID:30773278 1614311 Tonsl tonsoku-like, DNA repair protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614311 Tonsl tonsoku-like, DNA repair protein gene MP:0012131 small visceral yolk sac IAGP N RGD:5509061 20200220 MGI PMID:30773278 1614311 Tonsl tonsoku-like, DNA repair protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1614313 Ttc39c tetratricopeptide repeat domain 39C gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20240523 MGI 1614313 Ttc39c tetratricopeptide repeat domain 39C gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20240523 MGI 1614313 Ttc39c tetratricopeptide repeat domain 39C gene MP:0002608 increased hematocrit IEA N RGD:5509061 20240523 MGI 1614313 Ttc39c tetratricopeptide repeat domain 39C gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20240523 MGI 1614313 Ttc39c tetratricopeptide repeat domain 39C gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1614314 Zkscan3 zinc finger with KRAB and SCAN domains 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:28581889 1614314 Zkscan3 zinc finger with KRAB and SCAN domains 3 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20220217 MGI PMID:34504306 1614315 Eldr Egfr long non-coding downstream RNA gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24381249 1614318 Angptl1 angiopoietin-like 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20190808 MGI 1614318 Angptl1 angiopoietin-like 1 gene MP:0001304 cataract IEA N RGD:5509061 20190808 MGI 1614318 Angptl1 angiopoietin-like 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1614318 Angptl1 angiopoietin-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17676644 1614318 Angptl1 angiopoietin-like 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0000445 short snout IEA N RGD:5509061 20141003 MGI 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:15229603 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0000914 exencephaly IEA N RGD:5509061 20141003 MGI 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0001095 enlarged trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:15229603 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0002639 micrognathia IEA N RGD:5509061 20141003 MGI 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:15229603 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0003047 abnormal thoracic vertebrae morphology IEA N RGD:5509061 20141003 MGI 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:15229603 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0003456 absent tail IEA N RGD:5509061 20141003 MGI 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0003671 abnormal eyelid aperture IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0003675 kidney cyst IEA N RGD:5509061 20141003 MGI 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15229603 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15229603 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15229603 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:15229603 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:15229603 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:15229603 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0009744 postaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0009845 abnormal neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0010557 dilated pulmonary artery IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0010976 small lung lobe IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15229603 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:20704721 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0012675 enlarged floor plate IAGP N RGD:5509061 20141003 MGI PMID:15229603 1614323 Ptk7 PTK7 protein tyrosine kinase 7 gene MP:0030961 abnormal outer hair cell kinocilium location or orientation IAGP N RGD:5509061 20190725 MGI PMID:15229603 1614326 Amtn amelotin gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220811 MGI 1614326 Amtn amelotin gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1614326 Amtn amelotin gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20170525 MGI PMID:25715379 1614326 Amtn amelotin gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20170525 MGI PMID:25715379 1614326 Amtn amelotin gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1614326 Amtn amelotin gene MP:0010096 abnormal incisor color IAGP N RGD:5509061 20170525 MGI PMID:25715379 1614326 Amtn amelotin gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20180215 MGI PMID:25715379 1614327 Spaar small regulatory polypeptide of amino acid response gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20211104 MGI PMID:28024296 1614327 Spaar small regulatory polypeptide of amino acid response gene MP:0013161 enhanced muscle regeneration IAGP N RGD:5509061 20211104 MGI PMID:28024296 1614328 Fam83c family with sequence similarity 83, member C gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1614332 Cyp4f16 cytochrome P450, family 4, subfamily f, polypeptide 16 gene MP:0001513 limb grasping IEA N RGD:5509061 20210128 MGI 1614332 Cyp4f16 cytochrome P450, family 4, subfamily f, polypeptide 16 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1614332 Cyp4f16 cytochrome P450, family 4, subfamily f, polypeptide 16 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0001258 decreased body length IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0001661 extended life span IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0001921 reduced fertility IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0003981 decreased circulating phospholipid level IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0009130 increased white fat cell number IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0010046 decreased omental fat pad weight IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0011590 increased hormone-sensitive lipase activity IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0011940 decreased food intake IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0020237 increased proline level IAGP N RGD:5509061 20151112 MGI PMID:25934505 1614338 Maf1 MAF1 homolog, negative regulator of RNA polymerase III gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:25934505 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20220811 MGI 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220811 MGI 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220811 MGI 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20230601 MGI 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0001577 anemia IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220811 MGI 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210826 MGI 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0003717 pallor IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20220811 MGI 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20220811 MGI 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20220714 MGI PMID:35563652 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20220811 MGI 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0009931 abnormal skin appearance IEA N RGD:5509061 20230601 MGI 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1614339 Tmcc2 transmembrane and coiled-coil domains 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210520 MGI 1614340 Rnf122 ring finger protein 122 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20240627 MGI PMID:27506794 1614340 Rnf122 ring finger protein 122 gene MP:0008562 increased interferon-alpha secretion IAGP N RGD:5509061 20240627 MGI PMID:27506794 1614340 Rnf122 ring finger protein 122 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20240627 MGI PMID:27506794 1614340 Rnf122 ring finger protein 122 gene MP:0008573 increased circulating interferon-alpha level IAGP N RGD:5509061 20240627 MGI PMID:27506794 1614340 Rnf122 ring finger protein 122 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20240627 MGI PMID:27506794 1614340 Rnf122 ring finger protein 122 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20240627 MGI PMID:27506794 1614340 Rnf122 ring finger protein 122 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20240627 MGI PMID:27506794 1614340 Rnf122 ring finger protein 122 gene MP:0031023 decreased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20240627 MGI PMID:27506794 1614342 Lrrn4cl LRRN4 C-terminal like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240502 MGI PMID:33758365 1614344 Foxk2 forkhead box K2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1614344 Foxk2 forkhead box K2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1614344 Foxk2 forkhead box K2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200310 MGI 1614344 Foxk2 forkhead box K2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1614344 Foxk2 forkhead box K2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0001263 weight loss IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0001270 distended abdomen IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0002083 premature death IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0005150 cachexia IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0011747 myelofibrosis IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0013414 decreased myeloid cell number in bone marrow IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0013658 abnormal myeloid cell morphology IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0013660 abnormal bone marrow hematopoietic cell morphology IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0013696 increased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0013704 increased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614345 Zfand2b zinc finger, AN1 type domain 2B gene MP:0013891 increased common myeloid progenitor cell number IAGP N RGD:5509061 20211104 MGI PMID:26692333 1614346 Btbd10 BTB domain containing 10 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230119 MGI 1614346 Btbd10 BTB domain containing 10 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230119 MGI 1614349 Tespa1 thymocyte expressed, positive selection associated 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:22561606 1614349 Tespa1 thymocyte expressed, positive selection associated 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22561606 1614349 Tespa1 thymocyte expressed, positive selection associated 1 gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:22561606 1614349 Tespa1 thymocyte expressed, positive selection associated 1 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22561606 1614349 Tespa1 thymocyte expressed, positive selection associated 1 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22561606 1614349 Tespa1 thymocyte expressed, positive selection associated 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22561606 1614349 Tespa1 thymocyte expressed, positive selection associated 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22561606 1614349 Tespa1 thymocyte expressed, positive selection associated 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22561606 1614349 Tespa1 thymocyte expressed, positive selection associated 1 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22561606 1614349 Tespa1 thymocyte expressed, positive selection associated 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22561606 1614349 Tespa1 thymocyte expressed, positive selection associated 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22561606 1614349 Tespa1 thymocyte expressed, positive selection associated 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22561606 1614349 Tespa1 thymocyte expressed, positive selection associated 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:22561606 1614349 Tespa1 thymocyte expressed, positive selection associated 1 gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:22561606 1614351 Ubl4b ubiquitin-like 4B gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1614351 Ubl4b ubiquitin-like 4B gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1614351 Ubl4b ubiquitin-like 4B gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1614351 Ubl4b ubiquitin-like 4B gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1614351 Ubl4b ubiquitin-like 4B gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1614351 Ubl4b ubiquitin-like 4B gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1614351 Ubl4b ubiquitin-like 4B gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1614352 Tmem35a transmembrane protein 35A gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:27170659 1614352 Tmem35a transmembrane protein 35A gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200310 MGI PMID:27170659 1614352 Tmem35a transmembrane protein 35A gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20200310 MGI PMID:27170659 1614352 Tmem35a transmembrane protein 35A gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20200310 MGI PMID:27170659 1614352 Tmem35a transmembrane protein 35A gene MP:0002806 abnormal conditioned emotional response IAGP N RGD:5509061 20200310 MGI PMID:27170659 1614352 Tmem35a transmembrane protein 35A gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20200310 MGI PMID:27170659 1614352 Tmem35a transmembrane protein 35A gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20200310 MGI PMID:27170659 1614352 Tmem35a transmembrane protein 35A gene MP:0009078 adrenal gland hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:27170659 1614352 Tmem35a transmembrane protein 35A gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20200310 MGI PMID:27170659 1614352 Tmem35a transmembrane protein 35A gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20200310 MGI PMID:27170659 1614352 Tmem35a transmembrane protein 35A gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:27170659 1614353 Slc25a30 solute carrier family 25, member 30 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20150430 MGI 1614353 Slc25a30 solute carrier family 25, member 30 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150430 MGI 1614353 Slc25a30 solute carrier family 25, member 30 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20160114 MGI 1614353 Slc25a30 solute carrier family 25, member 30 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1614353 Slc25a30 solute carrier family 25, member 30 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20141003 MGI 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0000414 alopecia IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0001192 scaly skin IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0001194 dermatitis IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0003677 abnormal ear lobe morphology IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20200310 MGI PMID:22572823 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20200730 MGI PMID:32220963 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20200730 MGI PMID:32220963 1614355 Gpr89 G protein-coupled receptor 89 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20200730 MGI PMID:32220963 1614357 Saysd1 SAYSVFN motif domain containing 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20240523 MGI 1614357 Saysd1 SAYSVFN motif domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240222 MGI PMID:37419030 1614357 Saysd1 SAYSVFN motif domain containing 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240222 MGI PMID:37419030 1614357 Saysd1 SAYSVFN motif domain containing 1 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20240523 MGI 1614357 Saysd1 SAYSVFN motif domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1614358 Spmip5 sperm associated microtubule inner protein 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1614360 Ccdc50 coiled-coil domain containing 50 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1614360 Ccdc50 coiled-coil domain containing 50 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230601 MGI 1614360 Ccdc50 coiled-coil domain containing 50 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20240530 MGI PMID:34453126 1614360 Ccdc50 coiled-coil domain containing 50 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20240530 MGI PMID:34453126 1614360 Ccdc50 coiled-coil domain containing 50 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1614360 Ccdc50 coiled-coil domain containing 50 gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20240530 MGI PMID:34453126 1614360 Ccdc50 coiled-coil domain containing 50 gene MP:0031025 decreased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20240530 MGI PMID:34453126 1614363 Fam3a FAM3 metabolism regulating signaling molecule A gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20201217 MGI PMID:28562339 1614363 Fam3a FAM3 metabolism regulating signaling molecule A gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20201217 MGI PMID:28562339 1614363 Fam3a FAM3 metabolism regulating signaling molecule A gene MP:0005015 increased T cell number IAGP N RGD:5509061 20201217 MGI PMID:28562339 1614363 Fam3a FAM3 metabolism regulating signaling molecule A gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20201217 MGI PMID:28562339 1614363 Fam3a FAM3 metabolism regulating signaling molecule A gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20201217 MGI PMID:28562339 1614363 Fam3a FAM3 metabolism regulating signaling molecule A gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20201217 MGI PMID:28562339 1614363 Fam3a FAM3 metabolism regulating signaling molecule A gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20201217 MGI PMID:28562339 1614363 Fam3a FAM3 metabolism regulating signaling molecule A gene MP:0011009 increased circulating glutamate dehydrogenase level IAGP N RGD:5509061 20201217 MGI PMID:28562339 1614363 Fam3a FAM3 metabolism regulating signaling molecule A gene MP:0012659 decreased superoxide dismutase level IAGP N RGD:5509061 20201217 MGI PMID:28562339 1614364 Smim8 small integral membrane protein 8 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1614364 Smim8 small integral membrane protein 8 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1614364 Smim8 small integral membrane protein 8 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210520 MGI 1614364 Smim8 small integral membrane protein 8 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1614364 Smim8 small integral membrane protein 8 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 1614364 Smim8 small integral membrane protein 8 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 1614364 Smim8 small integral membrane protein 8 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1614366 Smim20 small integral membrane protein 20 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20240801 MGI PMID:38733120 1614366 Smim20 small integral membrane protein 20 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20240801 MGI PMID:38733120 1614366 Smim20 small integral membrane protein 20 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20240801 MGI PMID:38733120 1614366 Smim20 small integral membrane protein 20 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20240801 MGI PMID:38733120 1614366 Smim20 small integral membrane protein 20 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20240801 MGI PMID:38733120 1614366 Smim20 small integral membrane protein 20 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20230601 MGI 1614368 Cox16 cytochrome c oxidase assembly protein 16 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1614368 Cox16 cytochrome c oxidase assembly protein 16 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1614369 Retreg1 reticulophagy regulator 1 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20160616 MGI PMID:26040720 1614369 Retreg1 reticulophagy regulator 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20220519 MGI 1614369 Retreg1 reticulophagy regulator 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1614369 Retreg1 reticulophagy regulator 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20160616 MGI PMID:26040720 1614369 Retreg1 reticulophagy regulator 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20160616 MGI PMID:26040720 1614371 Ccdc28b coiled coil domain containing 28B gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20240208 MGI PMID:35653384 1614371 Ccdc28b coiled coil domain containing 28B gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20240208 MGI PMID:35653384 1614371 Ccdc28b coiled coil domain containing 28B gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20240208 MGI PMID:35653384 1614371 Ccdc28b coiled coil domain containing 28B gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20240208 MGI PMID:35653384 1614371 Ccdc28b coiled coil domain containing 28B gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20240208 MGI PMID:35653384 1614371 Ccdc28b coiled coil domain containing 28B gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20240208 MGI PMID:35653384 1614371 Ccdc28b coiled coil domain containing 28B gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20240208 MGI PMID:35653384 1614371 Ccdc28b coiled coil domain containing 28B gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20240208 MGI PMID:35653384 1614373 Tm4sf20 transmembrane 4 L six family member 20 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1614373 Tm4sf20 transmembrane 4 L six family member 20 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220519 MGI 1614375 Camk2n1 calcium/calmodulin-dependent protein kinase II inhibitor 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20240620 MGI PMID:33746041 1614375 Camk2n1 calcium/calmodulin-dependent protein kinase II inhibitor 1 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20240620 MGI PMID:33746041 1614375 Camk2n1 calcium/calmodulin-dependent protein kinase II inhibitor 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20240620 MGI PMID:33746041 1614375 Camk2n1 calcium/calmodulin-dependent protein kinase II inhibitor 1 gene MP:0006110 ventricular fibrillation IAGP N RGD:5509061 20240620 MGI PMID:33746041 1614375 Camk2n1 calcium/calmodulin-dependent protein kinase II inhibitor 1 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20240620 MGI PMID:33746041 1614375 Camk2n1 calcium/calmodulin-dependent protein kinase II inhibitor 1 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20240620 MGI PMID:33746041 1614375 Camk2n1 calcium/calmodulin-dependent protein kinase II inhibitor 1 gene MP:0031217 increased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20240620 MGI PMID:33746041 1614375 Camk2n1 calcium/calmodulin-dependent protein kinase II inhibitor 1 gene MP:0031252 abnormal physiological response to hypoxia IAGP N RGD:5509061 20240620 MGI PMID:33746041 1614377 Hsbp1l1 heat shock factor binding protein 1-like 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201022 MGI 1614377 Hsbp1l1 heat shock factor binding protein 1-like 1 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20201022 MGI 1614377 Hsbp1l1 heat shock factor binding protein 1-like 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1614379 Kcne5 potassium voltage-gated channel subfamily E regulatory subunit 5 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20240606 MGI PMID:30289750 1614379 Kcne5 potassium voltage-gated channel subfamily E regulatory subunit 5 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20240606 MGI PMID:30289750 1614379 Kcne5 potassium voltage-gated channel subfamily E regulatory subunit 5 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20240606 MGI PMID:30289750 1614379 Kcne5 potassium voltage-gated channel subfamily E regulatory subunit 5 gene MP:0020345 abnormal myocardial fiber currents IAGP N RGD:5509061 20240606 MGI PMID:30289750 1614383 Lce1m late cornified envelope 1M gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1614385 Pes1 pescadillo ribosomal biogenesis factor 1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20210128 MGI 1614385 Pes1 pescadillo ribosomal biogenesis factor 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12237316 1614385 Pes1 pescadillo ribosomal biogenesis factor 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12237316 1614385 Pes1 pescadillo ribosomal biogenesis factor 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1614385 Pes1 pescadillo ribosomal biogenesis factor 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1614385 Pes1 pescadillo ribosomal biogenesis factor 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 1614385 Pes1 pescadillo ribosomal biogenesis factor 1 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1614385 Pes1 pescadillo ribosomal biogenesis factor 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12237316 1614385 Pes1 pescadillo ribosomal biogenesis factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614385 Pes1 pescadillo ribosomal biogenesis factor 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1614385 Pes1 pescadillo ribosomal biogenesis factor 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0000745 tremors IEA N RGD:5509061 20210520 MGI 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0001147 small testis IAGP N RGD:5509061 20160929 MGI PMID:26667018 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20160929 MGI PMID:26667018 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0001921 reduced fertility IAGP N RGD:5509061 20160929 MGI PMID:26667018 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0001935 decreased litter size IAGP N RGD:5509061 20160929 MGI PMID:26667018 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20160811 MGI 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20160929 MGI PMID:26667018 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20170105 MGI 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20160929 MGI PMID:26667018 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20160929 MGI PMID:26667018 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20160929 MGI PMID:26667018 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20170105 MGI 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20170105 MGI 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20160929 MGI PMID:26667018 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20160929 MGI PMID:26667018 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20170105 MGI 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1614389 Knstrn kinetochore-localized astrin/SPAG5 binding gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20160929 MGI PMID:26667018 1614393 Mga MAX gene associated gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20160804 MGI PMID:25516968 1614393 Mga MAX gene associated gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20160804 MGI PMID:25516968 1614393 Mga MAX gene associated gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20160804 MGI PMID:25516968 1614393 Mga MAX gene associated gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20160804 MGI PMID:25516968 1614393 Mga MAX gene associated gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20160804 MGI PMID:25516968 1614393 Mga MAX gene associated gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20160804 MGI PMID:25516968 1614393 Mga MAX gene associated gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20160804 MGI PMID:25516968 1614393 Mga MAX gene associated gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20160804 MGI PMID:25516968 1614393 Mga MAX gene associated gene MP:0012743 increased inner cell mass apoptosis IAGP N RGD:5509061 20160804 MGI PMID:25516968 1614393 Mga MAX gene associated gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20160804 MGI PMID:25516968 1614395 Chaf1a chromatin assembly factor 1, subunit A gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17083276 1614395 Chaf1a chromatin assembly factor 1, subunit A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:17083276 1614395 Chaf1a chromatin assembly factor 1, subunit A gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17083276 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:11262229 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18057104 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:11262229 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:11262229 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20141003 MGI PMID:11262229 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:11262229 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11262229 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:21852535 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:11262229 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:11262229 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17199041 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10520993 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:11262229 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21852535 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:11262229 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:21852535 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:21852535 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:10520993 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:17199041 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:21852535 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21852535 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:21852535 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21852535 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:11262229 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21852535 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17199041 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:18057104 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21852535 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:21852535 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0010382 abnormal dosage compensation, by inactivation of X chromosome IAGP N RGD:5509061 20141003 MGI PMID:10520993 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0010382 abnormal dosage compensation, by inactivation of X chromosome IAGP N RGD:5509061 20141003 MGI PMID:21852535 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17199041 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15992549 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11262229 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0011103 embryonic lethality at implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17199041 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18057104 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0011200 abnormal extraembryonic coelom morphology IAGP N RGD:5509061 20141003 MGI PMID:11262229 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0011202 abnormal ectoplacental cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:11262229 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0012100 absent spongiotrophoblast IAGP N RGD:5509061 20141003 MGI PMID:21852535 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0012104 small amniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:11262229 1614402 Tsix X (inactive)-specific transcript, opposite strand gene MP:0020329 decreased capillary density IAGP N RGD:5509061 20160714 MGI PMID:21852535 1614410 Trip6 thyroid hormone receptor interactor 6 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20200402 MGI 1614410 Trip6 thyroid hormone receptor interactor 6 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20190502 MGI 1614410 Trip6 thyroid hormone receptor interactor 6 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20220908 MGI PMID:34620853 1614410 Trip6 thyroid hormone receptor interactor 6 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20220908 MGI PMID:34620853 1614410 Trip6 thyroid hormone receptor interactor 6 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20220908 MGI PMID:34620853 1614410 Trip6 thyroid hormone receptor interactor 6 gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20220908 MGI PMID:34620853 1614410 Trip6 thyroid hormone receptor interactor 6 gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20220811 MGI 1614410 Trip6 thyroid hormone receptor interactor 6 gene MP:0030964 decreased brain ependyma motile cilium length IAGP N RGD:5509061 20220908 MGI PMID:34620853 1614410 Trip6 thyroid hormone receptor interactor 6 gene MP:0030966 decreased brain ependyma motile cilium number IAGP N RGD:5509061 20220908 MGI PMID:34620853 1614411 Trap1a tumor rejection antigen P1A gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22140254 1614411 Trap1a tumor rejection antigen P1A gene MP:0005000 abnormal immune tolerance IAGP N RGD:5509061 20141003 MGI PMID:22140254 1614411 Trap1a tumor rejection antigen P1A gene MP:0005002 abnormal T cell clonal deletion IAGP N RGD:5509061 20141003 MGI PMID:22140254 1614411 Trap1a tumor rejection antigen P1A gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22140254 1614411 Trap1a tumor rejection antigen P1A gene MP:0010537 tumor regression IAGP N RGD:5509061 20141003 MGI PMID:22140254 1614412 Traf5 TNF receptor-associated factor 5 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:10449775 1614412 Traf5 TNF receptor-associated factor 5 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10449775 1614412 Traf5 TNF receptor-associated factor 5 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10449775 1614412 Traf5 TNF receptor-associated factor 5 gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10449775 1614412 Traf5 TNF receptor-associated factor 5 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:10449775 1614413 Traf1 TNF receptor-associated factor 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11672546 1614413 Traf1 TNF receptor-associated factor 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11672546 1614413 Traf1 TNF receptor-associated factor 1 gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:11672546 1614413 Traf1 TNF receptor-associated factor 1 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:11672546 1614414 Tmie transmembrane inner ear gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14027064 1614414 Tmie transmembrane inner ear gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:14027064 1614414 Tmie transmembrane inner ear gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:12140191 1614414 Tmie transmembrane inner ear gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:16235133 1614414 Tmie transmembrane inner ear gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:17219777 1614414 Tmie transmembrane inner ear gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:14027064 1614414 Tmie transmembrane inner ear gene MP:0001410 head bobbing IEA N RGD:5509061 20201022 MGI 1614414 Tmie transmembrane inner ear gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20141003 MGI PMID:12140191 1614414 Tmie transmembrane inner ear gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:14027064 1614414 Tmie transmembrane inner ear gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:16235133 1614414 Tmie transmembrane inner ear gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:17219777 1614414 Tmie transmembrane inner ear gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1614414 Tmie transmembrane inner ear gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:14027064 1614414 Tmie transmembrane inner ear gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:16235133 1614414 Tmie transmembrane inner ear gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:14027064 1614414 Tmie transmembrane inner ear gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1614414 Tmie transmembrane inner ear gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:12140191 1614414 Tmie transmembrane inner ear gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:14027064 1614414 Tmie transmembrane inner ear gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:14027064 1614414 Tmie transmembrane inner ear gene MP:0003150 detached tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:14027064 1614414 Tmie transmembrane inner ear gene MP:0004331 vestibular saccular macula degeneration IAGP N RGD:5509061 20141003 MGI PMID:14027064 1614414 Tmie transmembrane inner ear gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:14027064 1614414 Tmie transmembrane inner ear gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 1614414 Tmie transmembrane inner ear gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:12140191 1614414 Tmie transmembrane inner ear gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17219777 1614414 Tmie transmembrane inner ear gene MP:0005191 head tilt IEA N RGD:5509061 20111116 MGI 1614414 Tmie transmembrane inner ear gene MP:0005655 increased aggression IEA N RGD:5509061 20201022 MGI 1614414 Tmie transmembrane inner ear gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:19648608 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0000649 sebaceous gland atrophy IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:16216550 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19648608 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0002965 increased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0003192 increased cholesterol efflux IAGP N RGD:5509061 20141003 MGI PMID:19648608 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:16216550 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:19648608 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19648608 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0008117 abnormal Langerhans cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0009160 abnormal pancreatic acinar cell zymogen granule morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0009441 delayed skin barrier formation IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0009560 absent epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20141003 MGI PMID:19648608 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16216550 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20141003 MGI PMID:23633022 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0013307 increased adrenal gland weight IAGP N RGD:5509061 20141120 MGI PMID:19897935 1614415 Sptlc2 serine palmitoyltransferase, long chain base subunit 2 gene MP:0013407 abnormal dendritic epidermal T cell morphology IAGP N RGD:5509061 20141225 MGI PMID:23633022 1614421 Sprr2f small proline-rich protein 2F gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20210325 MGI PMID:33017192 1614421 Sprr2f small proline-rich protein 2F gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20210325 MGI PMID:33017192 1614421 Sprr2f small proline-rich protein 2F gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210325 MGI PMID:33017192 1614421 Sprr2f small proline-rich protein 2F gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20210325 MGI PMID:33017192 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230119 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230119 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20230601 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0001785 edema IEA N RGD:5509061 20230601 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20230601 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17374614 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230119 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0002958 cerebral aqueductal stenosis IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230119 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20230601 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20230601 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0010733 abnormal axon initial segment morphology IAGP N RGD:5509061 20141003 MGI PMID:22632975 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20230601 MGI 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:22159418 1614426 Sptan1 spectrin alpha, non-erythrocytic 1 gene MP:0014561 decreased cortical ventricular zone cell density IAGP N RGD:5509061 20241031 MGI PMID:22159418 1614430 Serpina3g serine (or cysteine) peptidase inhibitor, clade A, member 3G gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:22745374 1614430 Serpina3g serine (or cysteine) peptidase inhibitor, clade A, member 3G gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22745374 1614430 Serpina3g serine (or cysteine) peptidase inhibitor, clade A, member 3G gene MP:0010833 abnormal memory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22745374 1614430 Serpina3g serine (or cysteine) peptidase inhibitor, clade A, member 3G gene MP:0010839 decreased CD8-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22745374 1614431 Serpina3k serine (or cysteine) peptidase inhibitor, clade A, member 3K gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20241114 MGI PMID:37175519 1614431 Serpina3k serine (or cysteine) peptidase inhibitor, clade A, member 3K gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20241114 MGI PMID:37175519 1614431 Serpina3k serine (or cysteine) peptidase inhibitor, clade A, member 3K gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20241114 MGI PMID:37175519 1614431 Serpina3k serine (or cysteine) peptidase inhibitor, clade A, member 3K gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20241114 MGI PMID:37175519 1614431 Serpina3k serine (or cysteine) peptidase inhibitor, clade A, member 3K gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20241114 MGI PMID:37175519 1614431 Serpina3k serine (or cysteine) peptidase inhibitor, clade A, member 3K gene MP:0031252 abnormal physiological response to hypoxia IAGP N RGD:5509061 20241114 MGI PMID:37175519 1614433 Serpinb9c serine (or cysteine) peptidase inhibitor, clade B, member 9c gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1614434 Serpinb9b serine (or cysteine) peptidase inhibitor, clade B, member 9b gene MP:0012564 decreased tumor incidence following infection IAGP N RGD:5509061 20241114 MGI PMID:36103821 1614438 Serpina1b serine (or cysteine) preptidase inhibitor, clade A, member 1B gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15516792 1614439 Serpina1a serine (or cysteine) peptidase inhibitor, clade A, member 1A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21574874 1614439 Serpina1a serine (or cysteine) peptidase inhibitor, clade A, member 1A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21574874 1614439 Serpina1a serine (or cysteine) peptidase inhibitor, clade A, member 1A gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21574874 1614441 Nsd1 nuclear receptor-binding SET-domain protein 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:12805229 1614441 Nsd1 nuclear receptor-binding SET-domain protein 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12805229 1614441 Nsd1 nuclear receptor-binding SET-domain protein 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12805229 1614441 Nsd1 nuclear receptor-binding SET-domain protein 1 gene MP:0002174 abnormal gastrulation movements IAGP N RGD:5509061 20141003 MGI PMID:12805229 1614441 Nsd1 nuclear receptor-binding SET-domain protein 1 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:12805229 1614441 Nsd1 nuclear receptor-binding SET-domain protein 1 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:12805229 1614441 Nsd1 nuclear receptor-binding SET-domain protein 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12805229 1614441 Nsd1 nuclear receptor-binding SET-domain protein 1 gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:12805229 1614441 Nsd1 nuclear receptor-binding SET-domain protein 1 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:12805229 1614441 Nsd1 nuclear receptor-binding SET-domain protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12805229 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20141003 MGI 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0004700 abnormal circulating insulin-like growth factor I level IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614443 Npy6r neuropeptide Y receptor Y6 gene MP:0012311 decreased defecation amount IAGP N RGD:5509061 20141030 MGI PMID:24411939 1614445 Emc8 ER membrane protein complex subunit 8 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1614445 Emc8 ER membrane protein complex subunit 8 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200310 MGI 1614445 Emc8 ER membrane protein complex subunit 8 gene MP:0002546 mydriasis IEA N RGD:5509061 20200310 MGI 1614445 Emc8 ER membrane protein complex subunit 8 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1614445 Emc8 ER membrane protein complex subunit 8 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1614445 Emc8 ER membrane protein complex subunit 8 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1614445 Emc8 ER membrane protein complex subunit 8 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20200310 MGI 1614445 Emc8 ER membrane protein complex subunit 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:9635194 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20200310 MGI PMID:9635194 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20200310 MGI PMID:1459450 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:1459450 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000433 microcephaly IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000564 syndactyly IAGP N RGD:5509061 20200310 MGI PMID:22879379 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000585 kinked tail IAGP N RGD:5509061 20200310 MGI PMID:9635194 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20200310 MGI PMID:9520320 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:9520320 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:9520320 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000601 small liver IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000601 small liver IAGP N RGD:5509061 20200310 MGI PMID:9520320 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:22879379 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000852 small cerebellum IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000852 small cerebellum IAGP N RGD:5509061 20200310 MGI PMID:22879379 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20200310 MGI PMID:22879379 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000962 disorganized dorsal root ganglion IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20200310 MGI PMID:1459450 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20200310 MGI PMID:1459450 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20200310 MGI PMID:1459450 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:15716345 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:1577267 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20200310 MGI PMID:15716345 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20200310 MGI PMID:9635194 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20200310 MGI PMID:1459450 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20200310 MGI PMID:1577267 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:1459450 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:8287798 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:9635194 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20200310 MGI PMID:9635194 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20200310 MGI PMID:9635194 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:8287798 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001953 respiratory failure IAGP N RGD:5509061 20200310 MGI PMID:9635194 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:1577267 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:9635194 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20200310 MGI PMID:22879379 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0002188 small heart IAGP N RGD:5509061 20200310 MGI PMID:8287798 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0002188 small heart IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15716345 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200310 MGI PMID:8287798 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200310 MGI PMID:9635194 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20200310 MGI PMID:8287798 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0002989 small kidney IAGP N RGD:5509061 20200310 MGI PMID:8287798 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20200310 MGI PMID:1459450 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:8287798 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:9520320 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20200310 MGI PMID:8287798 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200310 MGI PMID:8287798 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:1459450 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20200310 MGI PMID:9635194 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0004670 small vertebral body IAGP N RGD:5509061 20200310 MGI PMID:9635194 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20200310 MGI PMID:1459450 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20200310 MGI PMID:9520320 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0005227 abnormal vertebral body development IAGP N RGD:5509061 20200310 MGI PMID:9635194 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20200310 MGI PMID:8287798 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:15716345 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0006408 dorsal root ganglion hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:1459450 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20200310 MGI PMID:1459450 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:15716345 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20200310 MGI PMID:1459450 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20200310 MGI PMID:22879379 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0010432 common ventricle IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0010811 decreased type II pneumocyte number IAGP N RGD:5509061 20200310 MGI PMID:15716345 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0010816 decreased type I pneumocyte number IAGP N RGD:5509061 20200310 MGI PMID:15716345 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0010986 abnormal mesonephric mesenchyme morphology IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:15716345 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:8287798 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15716345 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:1577267 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9635194 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15716345 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:1459450 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:1931830 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22879379 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:8287798 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:8404543 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:9635194 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011412 gonadal ridge hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0011875 absent stomach IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20200310 MGI PMID:12381668 1614446 Mycn v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived gene MP:0013267 first pharyngeal arch hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:1459449 1614453 Dnajb3 DnaJ heat shock protein family (Hsp40) member B3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1614453 Dnajb3 DnaJ heat shock protein family (Hsp40) member B3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1614453 Dnajb3 DnaJ heat shock protein family (Hsp40) member B3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1614453 Dnajb3 DnaJ heat shock protein family (Hsp40) member B3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1614454 Frat1 frequently rearranged in advanced T cell lymphomas gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10534617 1614454 Frat1 frequently rearranged in advanced T cell lymphomas gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15681612 1614455 Fpr3 formyl peptide receptor 3 gene MP:0000495 abnormal colon morphology IEA N RGD:5509061 20160811 MGI 1614455 Fpr3 formyl peptide receptor 3 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210826 MGI 1614455 Fpr3 formyl peptide receptor 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1614455 Fpr3 formyl peptide receptor 3 gene MP:0002581 abnormal ileum morphology IEA N RGD:5509061 20160811 MGI 1614455 Fpr3 formyl peptide receptor 3 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20211021 MGI 1614455 Fpr3 formyl peptide receptor 3 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20201231 MGI 1614455 Fpr3 formyl peptide receptor 3 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20191219 MGI PMID:31653840 1614455 Fpr3 formyl peptide receptor 3 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1614455 Fpr3 formyl peptide receptor 3 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20211021 MGI 1614455 Fpr3 formyl peptide receptor 3 gene MP:0011678 abnormal vomeronasal sensory neuron physiology IAGP N RGD:5509061 20191219 MGI PMID:31653840 1614456 Srgap2 SLIT-ROBO Rho GTPase activating protein 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20200310 MGI PMID:22559944 1614456 Srgap2 SLIT-ROBO Rho GTPase activating protein 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20200310 MGI PMID:22559944 1614456 Srgap2 SLIT-ROBO Rho GTPase activating protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22559944 1614457 Foxl1 forkhead box L1 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:9203584 1614457 Foxl1 forkhead box L1 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9203584 1614457 Foxl1 forkhead box L1 gene MP:0000478 delayed intestine development IAGP N RGD:5509061 20141003 MGI PMID:9203584 1614457 Foxl1 forkhead box L1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9203584 1614457 Foxl1 forkhead box L1 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:16469829 1614457 Foxl1 forkhead box L1 gene MP:0000501 abnormal digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:11162636 1614457 Foxl1 forkhead box L1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11162636 1614457 Foxl1 forkhead box L1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9203584 1614457 Foxl1 forkhead box L1 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15650110 1614457 Foxl1 forkhead box L1 gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:15650110 1614457 Foxl1 forkhead box L1 gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:15650110 1614457 Foxl1 forkhead box L1 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9203584 1614457 Foxl1 forkhead box L1 gene MP:0003892 abnormal gastric gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11162636 1614457 Foxl1 forkhead box L1 gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20141003 MGI PMID:9203584 1614457 Foxl1 forkhead box L1 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11162636 1614457 Foxl1 forkhead box L1 gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11162636 1614457 Foxl1 forkhead box L1 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:9203584 1614457 Foxl1 forkhead box L1 gene MP:0005211 increased stomach mucosa thickness IAGP N RGD:5509061 20141003 MGI PMID:11162636 1614457 Foxl1 forkhead box L1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15650110 1614457 Foxl1 forkhead box L1 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:9203584 1614457 Foxl1 forkhead box L1 gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20141003 MGI PMID:9203584 1614457 Foxl1 forkhead box L1 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:9203584 1614457 Foxl1 forkhead box L1 gene MP:0010797 abnormal pyloric gastric gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11162636 1614457 Foxl1 forkhead box L1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9203584 1614457 Foxl1 forkhead box L1 gene MP:0014077 ectopic Paneth cells IAGP N RGD:5509061 20160310 MGI PMID:16469829 1614458 Foxf2 forkhead box F2 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20171102 MGI PMID:12812790 1614458 Foxf2 forkhead box F2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:12812790 1614458 Foxf2 forkhead box F2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0004223 hypoplastic trabecular meshwork IAGP N RGD:5509061 20141003 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0004226 absent Schlemm's canal IAGP N RGD:5509061 20160414 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12812790 1614458 Foxf2 forkhead box F2 gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12812790 1614458 Foxf2 forkhead box F2 gene MP:0004537 abnormal palatine bone horizontal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12812790 1614458 Foxf2 forkhead box F2 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20141003 MGI PMID:12812790 1614458 Foxf2 forkhead box F2 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0005204 abnormal canal of Schlemm morphology IAGP N RGD:5509061 20141003 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0005208 abnormal iris stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0006223 optic nerve swelling IAGP N RGD:5509061 20141003 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:12812790 1614458 Foxf2 forkhead box F2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20171102 MGI PMID:12812790 1614458 Foxf2 forkhead box F2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:12812790 1614458 Foxf2 forkhead box F2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:12812790 1614458 Foxf2 forkhead box F2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:12812790 1614458 Foxf2 forkhead box F2 gene MP:0010704 abnormal optic canal morphology IAGP N RGD:5509061 20171207 MGI PMID:12812790 1614458 Foxf2 forkhead box F2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12812790 1614458 Foxf2 forkhead box F2 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141003 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0013742 absent ciliary body IAGP N RGD:5509061 20150416 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0013743 ciliary body hypoplasia IAGP N RGD:5509061 20150416 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0014163 abnormal ciliary muscle morphology IAGP N RGD:5509061 20160414 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0014164 abnormal ciliary process morphology IAGP N RGD:5509061 20160414 MGI PMID:22022403 1614458 Foxf2 forkhead box F2 gene MP:0030290 absent soft palate IAGP N RGD:5509061 20171102 MGI PMID:12812790 1614458 Foxf2 forkhead box F2 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:12812790 1614459 Foxd4 forkhead box D4 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1614459 Foxd4 forkhead box D4 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1614461 Foxc2 forkhead box C2 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20171005 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:10704385 1614461 Foxc2 forkhead box C2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:10704385 1614461 Foxc2 forkhead box C2 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:10704385 1614461 Foxc2 forkhead box C2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:10767326 1614461 Foxc2 forkhead box C2 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:10767326 1614461 Foxc2 forkhead box C2 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:10767326 1614461 Foxc2 forkhead box C2 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:15196959 1614461 Foxc2 forkhead box C2 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:15196959 1614461 Foxc2 forkhead box C2 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:15664398 1614461 Foxc2 forkhead box C2 gene MP:0001788 periorbital edema IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20231130 MGI PMID:26299482 1614461 Foxc2 forkhead box C2 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22522965 1614461 Foxc2 forkhead box C2 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0002218 increased lymph node number IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0002400 abnormal multipotent stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15664398 1614461 Foxc2 forkhead box C2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:22522965 1614461 Foxc2 forkhead box C2 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0002748 abnormal pulmonary valve morphology IAGP N RGD:5509061 20141003 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0002898 absent cartilage IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:10704385 1614461 Foxc2 forkhead box C2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:16498405 1614461 Foxc2 forkhead box C2 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:15664398 1614461 Foxc2 forkhead box C2 gene MP:0003201 extremity edema IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0003390 lymphedema IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0003390 lymphedema IAGP N RGD:5509061 20231130 MGI PMID:26299482 1614461 Foxc2 forkhead box C2 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10704385 1614461 Foxc2 forkhead box C2 gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0004017 duplex kidney IAGP N RGD:5509061 20141003 MGI PMID:10704385 1614461 Foxc2 forkhead box C2 gene MP:0004038 lymphangiectasis IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0004085 abnormal heartbeat IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0004095 ocular distichiasis IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0004105 cornea abrasion IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0004106 lymphatic vessel hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0004107 abnormal thoracic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:10767326 1614461 Foxc2 forkhead box C2 gene MP:0004318 absent incus IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0004443 absent supraoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0004445 small exoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0004447 small basioccipital bone IAGP N RGD:5509061 20171005 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0004456 small pterygoid bone IAGP N RGD:5509061 20171005 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:16498405 1614461 Foxc2 forkhead box C2 gene MP:0004537 abnormal palatine bone horizontal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0004604 abnormal vertebral pedicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0004605 abnormal vertebral lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0004670 small vertebral body IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0004706 short vertebral body IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15664398 1614461 Foxc2 forkhead box C2 gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20141003 MGI PMID:10767326 1614461 Foxc2 forkhead box C2 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0005199 abnormal iris pigment epithelium IAGP N RGD:5509061 20141003 MGI PMID:10767326 1614461 Foxc2 forkhead box C2 gene MP:0005203 abnormal trabecular meshwork morphology IAGP N RGD:5509061 20141003 MGI PMID:10767326 1614461 Foxc2 forkhead box C2 gene MP:0005204 abnormal canal of Schlemm morphology IAGP N RGD:5509061 20141003 MGI PMID:10767326 1614461 Foxc2 forkhead box C2 gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20231130 MGI PMID:26299482 1614461 Foxc2 forkhead box C2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16498405 1614461 Foxc2 forkhead box C2 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16498405 1614461 Foxc2 forkhead box C2 gene MP:0005327 abnormal mesangial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16498405 1614461 Foxc2 forkhead box C2 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:10767326 1614461 Foxc2 forkhead box C2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20171005 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0006064 abnormal superior vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0006230 iris stroma hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10767326 1614461 Foxc2 forkhead box C2 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:15196959 1614461 Foxc2 forkhead box C2 gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20141003 MGI PMID:16498405 1614461 Foxc2 forkhead box C2 gene MP:0008138 absent podocyte foot process IAGP N RGD:5509061 20141003 MGI PMID:16498405 1614461 Foxc2 forkhead box C2 gene MP:0008149 abnormal costovertebral joint morphology IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0008380 abnormal gonial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0008382 gonial bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20141003 MGI PMID:10704385 1614461 Foxc2 forkhead box C2 gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20141003 MGI PMID:15196959 1614461 Foxc2 forkhead box C2 gene MP:0009037 abnormal subarachnoid space development IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0009825 cornea ulcer IAGP N RGD:5509061 20150430 MGI PMID:10767326 1614461 Foxc2 forkhead box C2 gene MP:0009859 eye opacity IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0009929 meningomyelocele IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0010030 abnormal orbit morphology IAGP N RGD:5509061 20141003 MGI PMID:12719382 1614461 Foxc2 forkhead box C2 gene MP:0010326 malleus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:22522965 1614461 Foxc2 forkhead box C2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20231130 MGI PMID:26299482 1614461 Foxc2 forkhead box C2 gene MP:0010502 ventricle myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0010526 aortic arch coarctation IAGP N RGD:5509061 20141003 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0010526 aortic arch coarctation IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20141003 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0010605 thick pulmonary valve cusps IAGP N RGD:5509061 20141003 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0010701 fusion of atlas and odontoid process IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0010980 ectopic ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:10704385 1614461 Foxc2 forkhead box C2 gene MP:0010981 abnormal branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10704385 1614461 Foxc2 forkhead box C2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20231130 MGI PMID:26299482 1614461 Foxc2 forkhead box C2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10364424 1614461 Foxc2 forkhead box C2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15664398 1614461 Foxc2 forkhead box C2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:16498405 1614461 Foxc2 forkhead box C2 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16498405 1614461 Foxc2 forkhead box C2 gene MP:0011359 decreased glomerular capillary number IAGP N RGD:5509061 20141003 MGI PMID:16498405 1614461 Foxc2 forkhead box C2 gene MP:0011437 glomerulus hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16498405 1614461 Foxc2 forkhead box C2 gene MP:0011455 absent glomerular endothelium fenestra IAGP N RGD:5509061 20141003 MGI PMID:16498405 1614461 Foxc2 forkhead box C2 gene MP:0011493 double ureter IAGP N RGD:5509061 20141003 MGI PMID:10704385 1614461 Foxc2 forkhead box C2 gene MP:0011509 dilated glomerular capillary IAGP N RGD:5509061 20141003 MGI PMID:16498405 1614461 Foxc2 forkhead box C2 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231130 MGI PMID:26299482 1614461 Foxc2 forkhead box C2 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:10479458 1614461 Foxc2 forkhead box C2 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0012176 abnormal head development IAGP N RGD:5509061 20171214 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0012184 absent paraxial mesoderm IAGP N RGD:5509061 20141003 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0013200 head mesenchyme hypoplasia IAGP N RGD:5509061 20171214 MGI PMID:11562355 1614461 Foxc2 forkhead box C2 gene MP:0030026 small Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20171005 MGI PMID:9106663 1614461 Foxc2 forkhead box C2 gene MP:0030290 absent soft palate IAGP N RGD:5509061 20171102 MGI PMID:9409679 1614461 Foxc2 forkhead box C2 gene MP:0030337 enlarged third pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:11562355 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:10942411 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18178860 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7697542 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:18178860 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18178860 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:8639882 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18178860 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18178860 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18178860 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18178860 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18178860 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:18178860 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:18178860 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:18178860 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:18178860 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18178860 1614463 Csf2rb2 colony stimulating factor 2 receptor, beta 2, low-affinity (granulocyte-macrophage) gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18178860 1614464 Csf2ra colony stimulating factor 2 receptor, alpha, low-affinity (granulocyte-macrophage) gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20220428 MGI PMID:35043685 1614464 Csf2ra colony stimulating factor 2 receptor, alpha, low-affinity (granulocyte-macrophage) gene MP:0001861 lung inflammation IAGP N RGD:5509061 20220428 MGI PMID:35043685 1614464 Csf2ra colony stimulating factor 2 receptor, alpha, low-affinity (granulocyte-macrophage) gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20220428 MGI PMID:35043685 1614464 Csf2ra colony stimulating factor 2 receptor, alpha, low-affinity (granulocyte-macrophage) gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20220428 MGI PMID:35043685 1614464 Csf2ra colony stimulating factor 2 receptor, alpha, low-affinity (granulocyte-macrophage) gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20220428 MGI PMID:35043685 1614466 Crym crystallin, mu gene MP:0005472 abnormal triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:17264173 1614466 Crym crystallin, mu gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:17264173 1614466 Crym crystallin, mu gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:17264173 1614466 Crym crystallin, mu gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1614475 Alx3 aristaless-like homeobox 3 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:20534379 1614475 Alx3 aristaless-like homeobox 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:15728667 1614475 Alx3 aristaless-like homeobox 3 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:20534379 1614475 Alx3 aristaless-like homeobox 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20534379 1614475 Alx3 aristaless-like homeobox 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:20534379 1614475 Alx3 aristaless-like homeobox 3 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:20534379 1614475 Alx3 aristaless-like homeobox 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21104068 1614475 Alx3 aristaless-like homeobox 3 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20171102 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:21104068 1614475 Alx3 aristaless-like homeobox 3 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21104068 1614475 Alx3 aristaless-like homeobox 3 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:20534379 1614475 Alx3 aristaless-like homeobox 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20534379 1614475 Alx3 aristaless-like homeobox 3 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20534379 1614475 Alx3 aristaless-like homeobox 3 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0004459 small alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0004692 small pubis IAGP N RGD:5509061 20141003 MGI PMID:15728667 1614475 Alx3 aristaless-like homeobox 3 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20171123 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21104068 1614475 Alx3 aristaless-like homeobox 3 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21104068 1614475 Alx3 aristaless-like homeobox 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21104068 1614475 Alx3 aristaless-like homeobox 3 gene MP:0008430 short temporal bone squamous part IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:21104068 1614475 Alx3 aristaless-like homeobox 3 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:21104068 1614475 Alx3 aristaless-like homeobox 3 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:20534379 1614475 Alx3 aristaless-like homeobox 3 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20534379 1614475 Alx3 aristaless-like homeobox 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20534379 1614475 Alx3 aristaless-like homeobox 3 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:20534379 1614475 Alx3 aristaless-like homeobox 3 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20160324 MGI PMID:21104068 1614475 Alx3 aristaless-like homeobox 3 gene MP:0014117 increased pancreatic beta cell apoptosis IAGP N RGD:5509061 20160324 MGI PMID:21104068 1614475 Alx3 aristaless-like homeobox 3 gene MP:0030116 bifid nasal tip IAGP N RGD:5509061 20170928 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0030117 bifid nose IAGP N RGD:5509061 20170928 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0030301 abnormal maxillary frontal process morphology IAGP N RGD:5509061 20171102 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0030384 short facial bone IAGP N RGD:5509061 20171207 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0030385 absent facial bone IAGP N RGD:5509061 20171207 MGI PMID:11641221 1614475 Alx3 aristaless-like homeobox 3 gene MP:0030388 large fontanelles IAGP N RGD:5509061 20171207 MGI PMID:11641221 1614519 Rbm24 RNA binding motif protein 24 gene MP:0000299 failure of atrioventricular cushion closure IAGP N RGD:5509061 20180503 MGI PMID:29358667 1614519 Rbm24 RNA binding motif protein 24 gene MP:0000300 thin atrioventricular cushion IAGP N RGD:5509061 20180503 MGI PMID:29358667 1614519 Rbm24 RNA binding motif protein 24 gene MP:0001263 weight loss IAGP N RGD:5509061 20221229 MGI PMID:30267374 1614519 Rbm24 RNA binding motif protein 24 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20221229 MGI PMID:30267374 1614519 Rbm24 RNA binding motif protein 24 gene MP:0002083 premature death IAGP N RGD:5509061 20221229 MGI PMID:30267374 1614519 Rbm24 RNA binding motif protein 24 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20221229 MGI PMID:30267374 1614519 Rbm24 RNA binding motif protein 24 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20221229 MGI PMID:30267374 1614519 Rbm24 RNA binding motif protein 24 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180503 MGI PMID:29358667 1614519 Rbm24 RNA binding motif protein 24 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20221229 MGI PMID:30267374 1614519 Rbm24 RNA binding motif protein 24 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20221229 MGI PMID:30267374 1614519 Rbm24 RNA binding motif protein 24 gene MP:0004094 abnormal M line morphology IAGP N RGD:5509061 20221229 MGI PMID:30267374 1614519 Rbm24 RNA binding motif protein 24 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20180503 MGI PMID:29358667 1614519 Rbm24 RNA binding motif protein 24 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20221229 MGI PMID:30267374 1614519 Rbm24 RNA binding motif protein 24 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20221229 MGI PMID:30267374 1614519 Rbm24 RNA binding motif protein 24 gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20180503 MGI PMID:29358667 1614519 Rbm24 RNA binding motif protein 24 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20180503 MGI PMID:29358667 1614519 Rbm24 RNA binding motif protein 24 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20221229 MGI PMID:30267374 1614519 Rbm24 RNA binding motif protein 24 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180503 MGI PMID:29358667 1614519 Rbm24 RNA binding motif protein 24 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20221229 MGI PMID:30267374 1614519 Rbm24 RNA binding motif protein 24 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20180503 MGI PMID:29358667 1614519 Rbm24 RNA binding motif protein 24 gene MP:0031392 hypoactivity IAGP N RGD:5509061 20221229 MGI PMID:30267374 1614519 Rbm24 RNA binding motif protein 24 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:30267374 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0001633 poor circulation IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0001785 edema IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0003416 premature bone ossification IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0003717 pallor IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0004266 pale placenta IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0011206 absent visceral yolk sac IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0012301 absent umbilical cord blood vessels IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614554 Samd1 sterile alpha motif domain containing 1 gene MP:0031232 increased circulating angiotensin II level IAGP N RGD:5509061 20231109 MGI PMID:36810619 1614602 Vmn2r115 vomeronasal 2, receptor 115 gene MP:0001376 abnormal mating receptivity IAGP N RGD:5509061 20210225 MGI PMID:30367054 1614603 Cntnap5a contactin associated protein-like 5A gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1614603 Cntnap5a contactin associated protein-like 5A gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 1614603 Cntnap5a contactin associated protein-like 5A gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1614603 Cntnap5a contactin associated protein-like 5A gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20181227 MGI 1614607 Rergl RERG/RAS-like gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1614607 Rergl RERG/RAS-like gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 1614607 Rergl RERG/RAS-like gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210826 MGI 1614662 Psg26 pregnancy-specific beta-1-glycoprotein 26 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200402 MGI 1614667 Insyn2b inhibitory synaptic factor family member 2B gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20230601 MGI 1614667 Insyn2b inhibitory synaptic factor family member 2B gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1614667 Insyn2b inhibitory synaptic factor family member 2B gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1614667 Insyn2b inhibitory synaptic factor family member 2B gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1614667 Insyn2b inhibitory synaptic factor family member 2B gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1614668 Gpr17 G protein-coupled receptor 17 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1614668 Gpr17 G protein-coupled receptor 17 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:19838178 1614668 Gpr17 G protein-coupled receptor 17 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19838178 1614668 Gpr17 G protein-coupled receptor 17 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25624481 1614668 Gpr17 G protein-coupled receptor 17 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20220519 MGI 1614668 Gpr17 G protein-coupled receptor 17 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:19561298 1614670 Zc3h12b zinc finger CCCH-type containing 12B gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1614670 Zc3h12b zinc finger CCCH-type containing 12B gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 1614670 Zc3h12b zinc finger CCCH-type containing 12B gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1614670 Zc3h12b zinc finger CCCH-type containing 12B gene MP:0002637 small uterus IEA N RGD:5509061 20210826 MGI 1614670 Zc3h12b zinc finger CCCH-type containing 12B gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1614670 Zc3h12b zinc finger CCCH-type containing 12B gene MP:0009456 impaired cued conditioning behavior IEA N RGD:5509061 20210128 MGI 1614676 Mansc4 MANSC domain containing 4 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1614686 Zar1l zygote arrest 1-like gene MP:0003718 maternal effect IAGP N RGD:5509061 20210520 MGI PMID:31598710 1614686 Zar1l zygote arrest 1-like gene MP:0004024 aneuploidy IAGP N RGD:5509061 20210520 MGI PMID:31598710 1614686 Zar1l zygote arrest 1-like gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20210520 MGI PMID:31598710 1614686 Zar1l zygote arrest 1-like gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38786026 1614686 Zar1l zygote arrest 1-like gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20210520 MGI PMID:31598710 1614686 Zar1l zygote arrest 1-like gene MP:0014443 impaired polar body extrusion IAGP N RGD:5509061 20240509 MGI PMID:31598710 1614692 Dnm3os dynamin 3, opposite strand gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18985749 1614692 Dnm3os dynamin 3, opposite strand gene MP:0021186 decreased bone mineral density of vertebrae IAGP N RGD:5509061 20220915 MGI PMID:18985749 1614697 Dusp29 dual specificity phosphatase 29 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1614722 Tmem178b transmembrane protein 178B gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1614722 Tmem178b transmembrane protein 178B gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20201022 MGI 1614722 Tmem178b transmembrane protein 178B gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20200514 MGI 1614725 Zfp708 zinc finger protein 708 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20200806 MGI PMID:30846446 1614729 Prr7 proline rich 7 (synaptic) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20170126 MGI PMID:27657535 1614732 Gm5447 predicted gene 5447 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1614732 Gm5447 predicted gene 5447 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1614747 Primpol primase and polymerase (DNA-directed) gene MP:0000745 tremors IEA N RGD:5509061 20160421 MGI 1614747 Primpol primase and polymerase (DNA-directed) gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1614747 Primpol primase and polymerase (DNA-directed) gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1614747 Primpol primase and polymerase (DNA-directed) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24207056 1614747 Primpol primase and polymerase (DNA-directed) gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:24267451 1614747 Primpol primase and polymerase (DNA-directed) gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20170810 MGI PMID:26926109 1614749 Gfral GDNF family receptor alpha like gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20180329 MGI PMID:28953886 1614749 Gfral GDNF family receptor alpha like gene MP:0001433 polyphagia IAGP N RGD:5509061 20180329 MGI PMID:28953886 1614749 Gfral GDNF family receptor alpha like gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180329 MGI PMID:28953886 1614749 Gfral GDNF family receptor alpha like gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20180329 MGI PMID:28953886 1614749 Gfral GDNF family receptor alpha like gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180329 MGI PMID:28953886 1614749 Gfral GDNF family receptor alpha like gene MP:0010358 abnormal free fatty acids level IAGP N RGD:5509061 20180329 MGI PMID:28953886 1614749 Gfral GDNF family receptor alpha like gene MP:0011969 abnormal circulating triglyceride level IAGP N RGD:5509061 20180329 MGI PMID:28953886 1614751 Mir124a-1 microRNA 124a-1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:21857657 1614751 Mir124a-1 microRNA 124a-1 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21857657 1614751 Mir124a-1 microRNA 124a-1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:21857657 1614751 Mir124a-1 microRNA 124a-1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:21857657 1614751 Mir124a-1 microRNA 124a-1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21857657 1614751 Mir124a-1 microRNA 124a-1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21857657 1614751 Mir124a-1 microRNA 124a-1 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21857657 1614751 Mir124a-1 microRNA 124a-1 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:21857657 1614751 Mir124a-1 microRNA 124a-1 gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21857657 1614751 Mir124a-1 microRNA 124a-1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21857657 1614752 Mir122 microRNA 122 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0008990 abnormal Ito cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0010042 abnormal oval cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:22820288 1614752 Mir122 microRNA 122 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:22820290 1614752 Mir122 microRNA 122 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:22820288 1614753 Mir206 microRNA 206 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:20007902 1614753 Mir206 microRNA 206 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:20007902 1614753 Mir206 microRNA 206 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20007902 1614753 Mir206 microRNA 206 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20007902 1614753 Mir206 microRNA 206 gene MP:0004243 abnormal motor nerve collateral sprouting IAGP N RGD:5509061 20141003 MGI PMID:20007902 1614753 Mir206 microRNA 206 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:20007902 1614760 Kash5 KASH domain containing 5 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1614760 Kash5 KASH domain containing 5 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1614760 Kash5 KASH domain containing 5 gene MP:0001127 small ovary IAGP N RGD:5509061 20161208 MGI PMID:24062341 1614760 Kash5 KASH domain containing 5 gene MP:0001147 small testis IAGP N RGD:5509061 20161208 MGI PMID:24062341 1614760 Kash5 KASH domain containing 5 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20161208 MGI PMID:24062341 1614760 Kash5 KASH domain containing 5 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1614760 Kash5 KASH domain containing 5 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1614760 Kash5 KASH domain containing 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20161208 MGI PMID:24062341 1614760 Kash5 KASH domain containing 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20161208 MGI PMID:24062341 1614760 Kash5 KASH domain containing 5 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20161208 MGI PMID:24062341 1614760 Kash5 KASH domain containing 5 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20161208 MGI PMID:24062341 1614760 Kash5 KASH domain containing 5 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20161208 MGI PMID:24062341 1614760 Kash5 KASH domain containing 5 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1614760 Kash5 KASH domain containing 5 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1614760 Kash5 KASH domain containing 5 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20161208 MGI PMID:24062341 1614760 Kash5 KASH domain containing 5 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20161208 MGI PMID:24062341 1614760 Kash5 KASH domain containing 5 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20161208 MGI PMID:24062341 1614760 Kash5 KASH domain containing 5 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20161208 MGI PMID:24062341 1614760 Kash5 KASH domain containing 5 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1614760 Kash5 KASH domain containing 5 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230601 MGI 1614760 Kash5 KASH domain containing 5 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20161208 MGI PMID:24062341 1614760 Kash5 KASH domain containing 5 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20161208 MGI PMID:24062341 1614760 Kash5 KASH domain containing 5 gene MP:0030024 abnormal meiotic attachment of telomere to nuclear envelope IAGP N RGD:5509061 20170803 MGI PMID:24062341 1614769 Snx22 sorting nexin 22 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1614769 Snx22 sorting nexin 22 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1614769 Snx22 sorting nexin 22 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1614771 Foxr1 forkhead box R1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20231207 MGI 1614771 Foxr1 forkhead box R1 gene MP:0000692 small spleen IEA N RGD:5509061 20220519 MGI 1614771 Foxr1 forkhead box R1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20231207 MGI 1614771 Foxr1 forkhead box R1 gene MP:0001127 small ovary IEA N RGD:5509061 20220519 MGI 1614771 Foxr1 forkhead box R1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1614771 Foxr1 forkhead box R1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 1614771 Foxr1 forkhead box R1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1614773 Prdm10 PR domain containing 10 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160421 MGI 1614773 Prdm10 PR domain containing 10 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 1614773 Prdm10 PR domain containing 10 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 1614773 Prdm10 PR domain containing 10 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1614773 Prdm10 PR domain containing 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614773 Prdm10 PR domain containing 10 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210520 MGI 1614775 AB124611 cDNA sequence AB124611 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1614775 AB124611 cDNA sequence AB124611 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1614775 AB124611 cDNA sequence AB124611 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1614775 AB124611 cDNA sequence AB124611 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210520 MGI 1614775 AB124611 cDNA sequence AB124611 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210520 MGI 1614775 AB124611 cDNA sequence AB124611 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20240523 MGI 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18758446 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:18758446 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:18758446 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20171221 MGI PMID:22592058 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0001356 increased aggression towards female mice IAGP N RGD:5509061 20171221 MGI PMID:22592058 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20171221 MGI PMID:22592058 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20171221 MGI PMID:22592058 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20171221 MGI PMID:22592058 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20171221 MGI PMID:22592058 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:18758446 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20171221 MGI PMID:22592058 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18758446 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:18758446 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20171221 MGI PMID:22592058 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18758446 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18758446 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18758446 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20171221 MGI PMID:22592058 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20171221 MGI PMID:22592058 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:18758446 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:18758446 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18758446 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0008501 increased IgG2b level IEA N RGD:5509061 20160804 MGI 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0009081 thin uterus IAGP N RGD:5509061 20141003 MGI PMID:18758446 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20171221 MGI PMID:22592058 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0009710 anhedonia IAGP N RGD:5509061 20171221 MGI PMID:22592058 1614777 Crtc1 CREB regulated transcription coactivator 1 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20171221 MGI PMID:22592058 1614779 Gse1 genetic suppressor element 1, coiled-coil protein gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 1614779 Gse1 genetic suppressor element 1, coiled-coil protein gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1614779 Gse1 genetic suppressor element 1, coiled-coil protein gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20160804 MGI 1614779 Gse1 genetic suppressor element 1, coiled-coil protein gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1614779 Gse1 genetic suppressor element 1, coiled-coil protein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1614779 Gse1 genetic suppressor element 1, coiled-coil protein gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160804 MGI 1614779 Gse1 genetic suppressor element 1, coiled-coil protein gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160804 MGI 1614779 Gse1 genetic suppressor element 1, coiled-coil protein gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20160804 MGI 1614780 Unc13a unc-13 homolog A gene MP:0000746 weakness IAGP N RGD:5509061 20200310 MGI PMID:10440375 1614780 Unc13a unc-13 homolog A gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20200310 MGI PMID:17267576 1614780 Unc13a unc-13 homolog A gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:18703708 1614780 Unc13a unc-13 homolog A gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20200310 MGI PMID:18703708 1614780 Unc13a unc-13 homolog A gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20200310 MGI PMID:23770256 1614780 Unc13a unc-13 homolog A gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:11792326 1614780 Unc13a unc-13 homolog A gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:17267576 1614780 Unc13a unc-13 homolog A gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:21040848 1614780 Unc13a unc-13 homolog A gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20200310 MGI PMID:23770256 1614780 Unc13a unc-13 homolog A gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:16644700 1614780 Unc13a unc-13 homolog A gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:24814481 1614780 Unc13a unc-13 homolog A gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20200310 MGI PMID:12070347 1614780 Unc13a unc-13 homolog A gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20200310 MGI PMID:12070347 1614780 Unc13a unc-13 homolog A gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:17267576 1614780 Unc13a unc-13 homolog A gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20200310 MGI PMID:11792326 1614780 Unc13a unc-13 homolog A gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20200310 MGI PMID:17267576 1614780 Unc13a unc-13 homolog A gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20200310 MGI PMID:11792326 1614780 Unc13a unc-13 homolog A gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20200310 MGI PMID:10440375 1614780 Unc13a unc-13 homolog A gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20200310 MGI PMID:11792326 1614780 Unc13a unc-13 homolog A gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20200310 MGI PMID:12070347 1614780 Unc13a unc-13 homolog A gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20200310 MGI PMID:17267576 1614780 Unc13a unc-13 homolog A gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20200310 MGI PMID:21040848 1614780 Unc13a unc-13 homolog A gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20200310 MGI PMID:23770256 1614780 Unc13a unc-13 homolog A gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20200310 MGI PMID:16644700 1614780 Unc13a unc-13 homolog A gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:16644700 1614780 Unc13a unc-13 homolog A gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20200310 MGI PMID:10440375 1614780 Unc13a unc-13 homolog A gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20200310 MGI PMID:12070347 1614780 Unc13a unc-13 homolog A gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20200310 MGI PMID:18703708 1614780 Unc13a unc-13 homolog A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18703708 1614780 Unc13a unc-13 homolog A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10440375 1614780 Unc13a unc-13 homolog A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11792326 1614780 Unc13a unc-13 homolog A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12070347 1614780 Unc13a unc-13 homolog A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17267576 1614781 Ano8 anoctamin 8 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1614781 Ano8 anoctamin 8 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1614781 Ano8 anoctamin 8 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1614781 Ano8 anoctamin 8 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20190502 MGI 1614788 Begain brain-enriched guanylate kinase-associated gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20240822 MGI PMID:27785460 1614788 Begain brain-enriched guanylate kinase-associated gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20240822 MGI PMID:27785460 1614788 Begain brain-enriched guanylate kinase-associated gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20240822 MGI PMID:38086879 1614788 Begain brain-enriched guanylate kinase-associated gene MP:0011271 prolonged excitatory postsynaptic current rise time IAGP N RGD:5509061 20240822 MGI PMID:27785460 1614788 Begain brain-enriched guanylate kinase-associated gene MP:0012319 fast extinction of fear memory IAGP N RGD:5509061 20240822 MGI PMID:38086879 1614792 Atxn7l1 ataxin 7-like 1 gene MP:0000745 tremors IEA N RGD:5509061 20240523 MGI 1614792 Atxn7l1 ataxin 7-like 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1614792 Atxn7l1 ataxin 7-like 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1614792 Atxn7l1 ataxin 7-like 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 1614793 Milr1 mast cell immunoglobulin like receptor 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210128 MGI 1614793 Milr1 mast cell immunoglobulin like receptor 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1614793 Milr1 mast cell immunoglobulin like receptor 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1614793 Milr1 mast cell immunoglobulin like receptor 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1614793 Milr1 mast cell immunoglobulin like receptor 1 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:20526344 1614793 Milr1 mast cell immunoglobulin like receptor 1 gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:20526344 1614793 Milr1 mast cell immunoglobulin like receptor 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20210128 MGI 1614793 Milr1 mast cell immunoglobulin like receptor 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000084 abnormal fontanelle morphology IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000413 polyphalangy IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000448 pointed snout IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:23870131 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20160804 MGI 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23870131 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20170223 MGI PMID:20511334 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:23870131 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003342 accessory spleen IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003582 abnormal ovary development IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003670 dilated renal glomerular capsule IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0003942 abnormal urinary system development IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004017 duplex kidney IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004131 abnormal motile primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004450 presphenoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004539 absent maxilla IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0006198 enophthalmos IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0008534 enlarged fourth ventricle IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20170223 MGI PMID:20511334 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0010772 abnormal pollex morphology IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0010807 abnormal stomach position or orientation IAGP N RGD:5509061 20150129 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0010977 fused right lung lobes IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0011059 abnormal ependyma motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0011293 dilated nephron IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0011344 abnormal loop of Henle ascending limb thick segment morphology IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0011727 ectopic ovary IAGP N RGD:5509061 20141003 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0011998 decreased embryonic cilium length IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0012093 absent nodal flow IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0012667 split sternal manubrium IAGP N RGD:5509061 20141003 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0013197 decreased embryonic cilium number IAGP N RGD:5509061 20141120 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:19776033 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0014274 decreased respiration IAGP N RGD:5509061 20230810 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0014278 semilobar holoprosencephaly IAGP N RGD:5509061 20230810 MGI PMID:23454480 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0020383 decreased kidney epithelial cell primary cilium length IAGP N RGD:5509061 20161013 MGI PMID:21045211 1614795 Mks1 MKS transition zone complex subunit 1 gene MP:0030309 abnormal posterior cranial fossa morphology IAGP N RGD:5509061 20171109 MGI PMID:23454480 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0001280 loss of vibrissae IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15145948 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15145948 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0005161 hematuria IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0011420 pyuria IAGP N RGD:5509061 20141003 MGI PMID:23892722 1614796 Scarf1 scavenger receptor class F, member 1 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:23892722 1614797 Tmem102 transmembrane protein 102 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20190418 MGI PMID:23620790 1614797 Tmem102 transmembrane protein 102 gene MP:0011825 decreased cell chemotaxis IAGP N RGD:5509061 20190418 MGI PMID:23620790 1614797 Tmem102 transmembrane protein 102 gene MP:0020212 impaired leukocyte migration IAGP N RGD:5509061 20190418 MGI PMID:23620790 1614798 Shisa6 shisa family member 6 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20221215 MGI 1614798 Shisa6 shisa family member 6 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20221215 MGI 1614798 Shisa6 shisa family member 6 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1614798 Shisa6 shisa family member 6 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20190919 MGI PMID:28196692 1614798 Shisa6 shisa family member 6 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 1614798 Shisa6 shisa family member 6 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20221215 MGI 1614798 Shisa6 shisa family member 6 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20190919 MGI PMID:28196692 1614798 Shisa6 shisa family member 6 gene MP:0009198 abnormal male genitalia morphology IEA N RGD:5509061 20221215 MGI 1614799 Slc47a2 solute carrier family 47, member 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220519 MGI 1614799 Slc47a2 solute carrier family 47, member 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1614802 Dgkk diacylglycerol kinase kappa gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20211021 MGI 1614802 Dgkk diacylglycerol kinase kappa gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1614802 Dgkk diacylglycerol kinase kappa gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1614802 Dgkk diacylglycerol kinase kappa gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1614802 Dgkk diacylglycerol kinase kappa gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1614802 Dgkk diacylglycerol kinase kappa gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1614803 Shisa3 shisa family member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17481602 1614805 Fam185a family with sequence similarity 185, member A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1614805 Fam185a family with sequence similarity 185, member A gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1614805 Fam185a family with sequence similarity 185, member A gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1614805 Fam185a family with sequence similarity 185, member A gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 1614805 Fam185a family with sequence similarity 185, member A gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 1614805 Fam185a family with sequence similarity 185, member A gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1614805 Fam185a family with sequence similarity 185, member A gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220519 MGI 1614805 Fam185a family with sequence similarity 185, member A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1614805 Fam185a family with sequence similarity 185, member A gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220519 MGI 1614805 Fam185a family with sequence similarity 185, member A gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220519 MGI 1614805 Fam185a family with sequence similarity 185, member A gene MP:0009709 hydrometra IEA N RGD:5509061 20210826 MGI 1614805 Fam185a family with sequence similarity 185, member A gene MP:0011047 increased lung tissue damping IEA N RGD:5509061 20210826 MGI 1614807 Ttll10 tubulin tyrosine ligase-like family, member 10 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1614807 Ttll10 tubulin tyrosine ligase-like family, member 10 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20201022 MGI 1614807 Ttll10 tubulin tyrosine ligase-like family, member 10 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:15905332 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:15905332 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:17876667 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:15905332 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0001525 impaired balance IEA N RGD:5509061 20111116 MGI 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15905332 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:17876667 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:15905332 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:17876667 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0003986 small cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:15905332 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15905332 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17876667 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15905332 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15905332 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17876667 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:17876667 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0005191 head tilt IEA N RGD:5509061 20111116 MGI 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:17876667 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15905332 1614809 Lhfpl5 lipoma HMGIC fusion partner-like 5 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17876667 1614810 Clpsl2 colipase-like 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20240523 MGI 1614810 Clpsl2 colipase-like 2 gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20240523 MGI 1614818 Wscd2 WSC domain containing 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1614818 Wscd2 WSC domain containing 2 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1614818 Wscd2 WSC domain containing 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1614823 Fsd1l fibronectin type III and SPRY domain containing 1-like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614829 Adam1b a disintegrin and metallopeptidase domain 1b gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16407235 1614830 Selenov selenoprotein V gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1614838 Nlrc4 NLR family, CARD domain containing 4 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20200310 MGI PMID:15190255 1614838 Nlrc4 NLR family, CARD domain containing 4 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20210318 MGI PMID:32342103 1614838 Nlrc4 NLR family, CARD domain containing 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:16717117 1614838 Nlrc4 NLR family, CARD domain containing 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:16984919 1614838 Nlrc4 NLR family, CARD domain containing 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:16648852 1614838 Nlrc4 NLR family, CARD domain containing 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:16984919 1614838 Nlrc4 NLR family, CARD domain containing 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200310 MGI PMID:16407890 1614838 Nlrc4 NLR family, CARD domain containing 4 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20200310 MGI PMID:16407890 1614838 Nlrc4 NLR family, CARD domain containing 4 gene MP:0005571 decreased lactate dehydrogenase level IAGP N RGD:5509061 20210318 MGI PMID:32342103 1614838 Nlrc4 NLR family, CARD domain containing 4 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:15190255 1614838 Nlrc4 NLR family, CARD domain containing 4 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:20457908 1614838 Nlrc4 NLR family, CARD domain containing 4 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20210318 MGI PMID:32342103 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0000154 rib fusion IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20210805 MGI PMID:34142127 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20210805 MGI PMID:34142127 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0000592 short tail IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0001762 polyuria IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20957652 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23383134 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0002963 decreased urine protein level IAGP N RGD:5509061 20170202 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0003109 short femur IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0003870 decreased urine glucose level IAGP N RGD:5509061 20170202 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0003916 decreased heart left ventricle weight IAGP N RGD:5509061 20231221 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0004508 abnormal pectoral girdle bone morphology IAGP N RGD:5509061 20170202 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0004604 abnormal vertebral pedicle morphology IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20210805 MGI PMID:34142127 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20170202 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005451 abnormal body composition IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005540 decreased urine albumin level IAGP N RGD:5509061 20170202 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20170202 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20170202 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20170202 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0010325 abnormal malleus head morphology IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0011424 decreased urine uric acid level IAGP N RGD:5509061 20170202 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20170202 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0013285 abnormal renal filtration IAGP N RGD:5509061 20170202 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20170126 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231221 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0030106 small incus IAGP N RGD:5509061 20171005 MGI PMID:27815347 1614840 Scube3 signal peptide, CUB domain, EGF-like 3 gene MP:0030123 small middle ear ossicles IAGP N RGD:5509061 20171005 MGI PMID:27815347 1614842 Creg2 cellular repressor of E1A-stimulated genes 2 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1614842 Creg2 cellular repressor of E1A-stimulated genes 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1614842 Creg2 cellular repressor of E1A-stimulated genes 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210520 MGI 1614869 Hdx highly divergent homeobox gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20200514 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20221215 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20221215 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0000418 focal hair loss IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0000692 small spleen IEA N RGD:5509061 20200514 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0001399 hyperactivity IEA N RGD:5509061 20220428 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20220811 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210422 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0002064 seizures IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0002083 premature death IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20221215 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20221215 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0002989 small kidney IEA N RGD:5509061 20210422 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20221215 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20221215 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20200514 MGI 1614872 Nexmif neurite extension and migration factor gene MP:0013117 focal hair loss in thorax region IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0020510 increased dendritic spine length IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0020513 abnormal dendritic stubby spine morphology IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0020514 abnormal dendritic thin spine morphology IAGP N RGD:5509061 20201105 MGI PMID:31704787 1614872 Nexmif neurite extension and migration factor gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:31704787 1614874 Gm614 predicted gene 614 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230119 MGI 1614874 Gm614 predicted gene 614 gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20210812 MGI PMID:33193409 1614874 Gm614 predicted gene 614 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20210812 MGI PMID:33193409 1614875 Awat1 acyl-CoA wax alcohol acyltransferase 1 gene MP:0001337 dry eyes IAGP N RGD:5509061 20221117 MGI PMID:34113821 1614875 Awat1 acyl-CoA wax alcohol acyltransferase 1 gene MP:0001349 excessive tearing IAGP N RGD:5509061 20221117 MGI PMID:34113821 1614875 Awat1 acyl-CoA wax alcohol acyltransferase 1 gene MP:0001994 increased blinking frequency IAGP N RGD:5509061 20221117 MGI PMID:34113821 1614875 Awat1 acyl-CoA wax alcohol acyltransferase 1 gene MP:0005252 abnormal Meibomian gland morphology IAGP N RGD:5509061 20221117 MGI PMID:34113821 1614875 Awat1 acyl-CoA wax alcohol acyltransferase 1 gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20211021 MGI 1614875 Awat1 acyl-CoA wax alcohol acyltransferase 1 gene MP:0013386 enlarged Meibomian gland IAGP N RGD:5509061 20221117 MGI PMID:34113821 1614875 Awat1 acyl-CoA wax alcohol acyltransferase 1 gene MP:0013391 abnormal Meibomian gland physiology IAGP N RGD:5509061 20221117 MGI PMID:34113821 1614875 Awat1 acyl-CoA wax alcohol acyltransferase 1 gene MP:0014131 abnormal tear film morphology IAGP N RGD:5509061 20221117 MGI PMID:34113821 1614877 Zc4h2 zinc finger, C4H2 domain containing gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20201217 MGI PMID:31336385 1614877 Zc4h2 zinc finger, C4H2 domain containing gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20201217 MGI PMID:31336385 1614877 Zc4h2 zinc finger, C4H2 domain containing gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20201217 MGI PMID:31336385 1614877 Zc4h2 zinc finger, C4H2 domain containing gene MP:0002083 premature death IAGP N RGD:5509061 20201217 MGI PMID:31336385 1614877 Zc4h2 zinc finger, C4H2 domain containing gene MP:0004100 abnormal spinal cord interneuron morphology IAGP N RGD:5509061 20201217 MGI PMID:31336385 1614877 Zc4h2 zinc finger, C4H2 domain containing gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20201217 MGI PMID:31336385 1614877 Zc4h2 zinc finger, C4H2 domain containing gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20201217 MGI PMID:31336385 1614877 Zc4h2 zinc finger, C4H2 domain containing gene MP:0021101 abnormal ventral interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:31336385 1614877 Zc4h2 zinc finger, C4H2 domain containing gene MP:0021102 abnormal ventral interneuron 0 morphology IAGP N RGD:5509061 20220310 MGI PMID:31336385 1614877 Zc4h2 zinc finger, C4H2 domain containing gene MP:0021103 abnormal ventral interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:31336385 1614877 Zc4h2 zinc finger, C4H2 domain containing gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:31336385 1614877 Zc4h2 zinc finger, C4H2 domain containing gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:31336385 1614883 Myo16 myosin XVI gene MP:0000774 decreased brain size IAGP N RGD:5509061 20180118 MGI PMID:21946561 1614883 Myo16 myosin XVI gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20180118 MGI PMID:21946561 1614883 Myo16 myosin XVI gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20180118 MGI PMID:21946561 1614885 Scart2 scavenger receptor family member expressed on T cells 2 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20210128 MGI 1614885 Scart2 scavenger receptor family member expressed on T cells 2 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1614885 Scart2 scavenger receptor family member expressed on T cells 2 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 1614887 Garem2 GRB2 associated regulator of MAPK1 subtype 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20201015 MGI PMID:31718706 1614887 Garem2 GRB2 associated regulator of MAPK1 subtype 2 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20201015 MGI PMID:31718706 1614887 Garem2 GRB2 associated regulator of MAPK1 subtype 2 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20201015 MGI PMID:31718706 1614887 Garem2 GRB2 associated regulator of MAPK1 subtype 2 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20201015 MGI PMID:31718706 1614887 Garem2 GRB2 associated regulator of MAPK1 subtype 2 gene MP:0003063 increased coping response IAGP N RGD:5509061 20201015 MGI PMID:31718706 1614887 Garem2 GRB2 associated regulator of MAPK1 subtype 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20201015 MGI PMID:31718706 1614888 Tgm6 transglutaminase 6 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 1614888 Tgm6 transglutaminase 6 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20210318 MGI PMID:30287856 1614888 Tgm6 transglutaminase 6 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1614888 Tgm6 transglutaminase 6 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20200402 MGI 1614888 Tgm6 transglutaminase 6 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20201022 MGI 1614890 Exd1 exonuclease 3'-5' domain containing 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20181227 MGI 1614890 Exd1 exonuclease 3'-5' domain containing 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20181227 MGI 1614890 Exd1 exonuclease 3'-5' domain containing 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20181227 MGI 1614890 Exd1 exonuclease 3'-5' domain containing 1 gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20170601 MGI PMID:26669262 1614891 Pcyox1l prenylcysteine oxidase 1 like gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1614891 Pcyox1l prenylcysteine oxidase 1 like gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230601 MGI 1614891 Pcyox1l prenylcysteine oxidase 1 like gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1614891 Pcyox1l prenylcysteine oxidase 1 like gene MP:0002834 decreased heart weight IEA N RGD:5509061 20210128 MGI 1614891 Pcyox1l prenylcysteine oxidase 1 like gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210128 MGI 1614891 Pcyox1l prenylcysteine oxidase 1 like gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20210128 MGI 1614891 Pcyox1l prenylcysteine oxidase 1 like gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 1614891 Pcyox1l prenylcysteine oxidase 1 like gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20201022 MGI 1614891 Pcyox1l prenylcysteine oxidase 1 like gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1614891 Pcyox1l prenylcysteine oxidase 1 like gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20181227 MGI 1614891 Pcyox1l prenylcysteine oxidase 1 like gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 1614891 Pcyox1l prenylcysteine oxidase 1 like gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1614891 Pcyox1l prenylcysteine oxidase 1 like gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0001406 abnormal gait IEA N RGD:5509061 20240523 MGI 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20230316 MGI PMID:35842425 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20240523 MGI 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20240523 MGI 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20230316 MGI PMID:35842425 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0002833 increased heart weight IEA N RGD:5509061 20240523 MGI 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20230316 MGI PMID:35842425 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0002981 increased liver weight IAGP N RGD:5509061 20230316 MGI PMID:35842425 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0005376 homeostasis/metabolism phenotype IAGP N RGD:5509061 20230316 MGI PMID:35842425 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20230316 MGI PMID:35842425 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20230316 MGI PMID:35842425 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0010360 decreased liver free fatty acids level IAGP N RGD:5509061 20230316 MGI PMID:35842425 1614893 Iigp1c interferon inducible GTPase 1C gene MP:0010951 abnormal lipid oxidation IAGP N RGD:5509061 20230316 MGI PMID:35842425 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17784788 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:12855593 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12855593 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12855593 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17784788 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20181227 MGI 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:12855593 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:12855593 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:12855593 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:17784788 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12855593 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17784788 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:17784788 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:17784788 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:12855593 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17784788 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17784788 1614894 Ccnb1ip1 cyclin B1 interacting protein 1 gene MP:0008967 absent chiasmata formation IAGP N RGD:5509061 20141003 MGI PMID:17784788 1614897 Ogdhl oxoglutarate dehydrogenase-like gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1614898 Smcr8 Smith-Magenis syndrome chromosome region, candidate 8 homolog (human) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20190124 MGI PMID:30442666 1614898 Smcr8 Smith-Magenis syndrome chromosome region, candidate 8 homolog (human) gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20190124 MGI PMID:30442666 1614898 Smcr8 Smith-Magenis syndrome chromosome region, candidate 8 homolog (human) gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20170105 MGI PMID:27617292 1614898 Smcr8 Smith-Magenis syndrome chromosome region, candidate 8 homolog (human) gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20190124 MGI PMID:30442666 1614898 Smcr8 Smith-Magenis syndrome chromosome region, candidate 8 homolog (human) gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20190124 MGI PMID:30442666 1614898 Smcr8 Smith-Magenis syndrome chromosome region, candidate 8 homolog (human) gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190124 MGI PMID:30442666 1614898 Smcr8 Smith-Magenis syndrome chromosome region, candidate 8 homolog (human) gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20190124 MGI PMID:30442666 1614898 Smcr8 Smith-Magenis syndrome chromosome region, candidate 8 homolog (human) gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20170105 MGI PMID:27617292 1614898 Smcr8 Smith-Magenis syndrome chromosome region, candidate 8 homolog (human) gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20170105 MGI PMID:27617292 1614898 Smcr8 Smith-Magenis syndrome chromosome region, candidate 8 homolog (human) gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20190124 MGI PMID:30442666 1614898 Smcr8 Smith-Magenis syndrome chromosome region, candidate 8 homolog (human) gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20190124 MGI PMID:30442666 1614898 Smcr8 Smith-Magenis syndrome chromosome region, candidate 8 homolog (human) gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20190124 MGI PMID:30442666 1614898 Smcr8 Smith-Magenis syndrome chromosome region, candidate 8 homolog (human) gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20190124 MGI PMID:30442666 1614901 Gm12258 predicted gene 12258 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1614901 Gm12258 predicted gene 12258 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1614902 Sowaha sosondowah ankyrin repeat domain family member A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1614902 Sowaha sosondowah ankyrin repeat domain family member A gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1614902 Sowaha sosondowah ankyrin repeat domain family member A gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1614902 Sowaha sosondowah ankyrin repeat domain family member A gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1614902 Sowaha sosondowah ankyrin repeat domain family member A gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1614902 Sowaha sosondowah ankyrin repeat domain family member A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1614902 Sowaha sosondowah ankyrin repeat domain family member A gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1614902 Sowaha sosondowah ankyrin repeat domain family member A gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1614902 Sowaha sosondowah ankyrin repeat domain family member A gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 1614902 Sowaha sosondowah ankyrin repeat domain family member A gene MP:0009456 impaired cued conditioning behavior IEA N RGD:5509061 20211021 MGI 1614909 Msantd2 Myb/SANT-like DNA-binding domain containing 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220519 MGI 1614909 Msantd2 Myb/SANT-like DNA-binding domain containing 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210826 MGI 1614909 Msantd2 Myb/SANT-like DNA-binding domain containing 2 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20210826 MGI 1614909 Msantd2 Myb/SANT-like DNA-binding domain containing 2 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20210826 MGI 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0001147 small testis IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0001925 male infertility IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20230720 MGI 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0031374 abnormal manchette assembly IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614911 Cfap119 cilia and flagella associated protein 119 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20240307 MGI PMID:37601242 1614914 Hirip3 HIRA interacting protein 3 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 1614914 Hirip3 HIRA interacting protein 3 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20231207 MGI 1614914 Hirip3 HIRA interacting protein 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1614914 Hirip3 HIRA interacting protein 3 gene MP:0002176 increased brain weight IEA N RGD:5509061 20231207 MGI 1614914 Hirip3 HIRA interacting protein 3 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20231207 MGI 1614914 Hirip3 HIRA interacting protein 3 gene MP:0002833 increased heart weight IEA N RGD:5509061 20231207 MGI 1614914 Hirip3 HIRA interacting protein 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 1614914 Hirip3 HIRA interacting protein 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 1614914 Hirip3 HIRA interacting protein 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1614915 Ino80e INO80 complex subunit E gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 1614915 Ino80e INO80 complex subunit E gene MP:0003313 abnormal locomotor activation IEA N RGD:5509061 20160804 MGI 1614916 Atxn2l ataxin 2-like gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20201015 MGI PMID:32698485 1614916 Atxn2l ataxin 2-like gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20201015 MGI PMID:32698485 1614916 Atxn2l ataxin 2-like gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20201015 MGI PMID:32698485 1614916 Atxn2l ataxin 2-like gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20201015 MGI PMID:32698485 1614916 Atxn2l ataxin 2-like gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20201015 MGI PMID:32698485 1614916 Atxn2l ataxin 2-like gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20201015 MGI PMID:32698485 1614916 Atxn2l ataxin 2-like gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20201015 MGI PMID:32698485 1614917 Cog7 component of oligomeric golgi complex 7 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20240523 MGI 1614917 Cog7 component of oligomeric golgi complex 7 gene MP:0005544 cornea deposits IEA N RGD:5509061 20201022 MGI 1614917 Cog7 component of oligomeric golgi complex 7 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20201022 MGI 1614917 Cog7 component of oligomeric golgi complex 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614917 Cog7 component of oligomeric golgi complex 7 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1614918 Ldaf1 lipid droplet assembly factor 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20231207 MGI 1614918 Ldaf1 lipid droplet assembly factor 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1614918 Ldaf1 lipid droplet assembly factor 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20230601 MGI 1614918 Ldaf1 lipid droplet assembly factor 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 1614918 Ldaf1 lipid droplet assembly factor 1 gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20231207 MGI 1614918 Ldaf1 lipid droplet assembly factor 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20240523 MGI 1614919 Acsm4 acyl-CoA synthetase medium-chain family member 4 gene MP:0001003 abnormal olfactory receptor morphology IAGP N RGD:5509061 20141003 MGI PMID:17989651 1614919 Acsm4 acyl-CoA synthetase medium-chain family member 4 gene MP:0001460 abnormal olfactory discrimination memory IAGP N RGD:5509061 20141003 MGI PMID:17989651 1614919 Acsm4 acyl-CoA synthetase medium-chain family member 4 gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:17989651 1614919 Acsm4 acyl-CoA synthetase medium-chain family member 4 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:17989651 1614919 Acsm4 acyl-CoA synthetase medium-chain family member 4 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17989651 1614921 Vwde von Willebrand factor D and EGF domains gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20220630 MGI PMID:34957547 1614921 Vwde von Willebrand factor D and EGF domains gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20220630 MGI PMID:34957547 1614921 Vwde von Willebrand factor D and EGF domains gene MP:0013129 abnormal tooth color IAGP N RGD:5509061 20220630 MGI PMID:34957547 1614922 Caprin2 caprin family member 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20160519 MGI PMID:26177727 1614922 Caprin2 caprin family member 2 gene MP:0001304 cataract IAGP N RGD:5509061 20160519 MGI PMID:26177727 1614922 Caprin2 caprin family member 2 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20160519 MGI PMID:26177727 1614922 Caprin2 caprin family member 2 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20160519 MGI PMID:26177727 1614922 Caprin2 caprin family member 2 gene MP:0010713 corneal-lenticular stalk IAGP N RGD:5509061 20160519 MGI PMID:26177727 1614923 Stk38l serine/threonine kinase 38 like gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20190905 MGI PMID:30135513 1614923 Stk38l serine/threonine kinase 38 like gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20190905 MGI PMID:30135513 1614923 Stk38l serine/threonine kinase 38 like gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20190905 MGI PMID:30135513 1614923 Stk38l serine/threonine kinase 38 like gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20150108 MGI PMID:24719112 1614923 Stk38l serine/threonine kinase 38 like gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20190905 MGI PMID:30135513 1614924 Slc10a4 solute carrier family 10 (sodium/bile acid cotransporter family), member 4 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:23022458 1614924 Slc10a4 solute carrier family 10 (sodium/bile acid cotransporter family), member 4 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:23022458 1614924 Slc10a4 solute carrier family 10 (sodium/bile acid cotransporter family), member 4 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:23022458 1614924 Slc10a4 solute carrier family 10 (sodium/bile acid cotransporter family), member 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1614924 Slc10a4 solute carrier family 10 (sodium/bile acid cotransporter family), member 4 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1614926 Znhit6 zinc finger, HIT type 6 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1614926 Znhit6 zinc finger, HIT type 6 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1614926 Znhit6 zinc finger, HIT type 6 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1614926 Znhit6 zinc finger, HIT type 6 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1614926 Znhit6 zinc finger, HIT type 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614926 Znhit6 zinc finger, HIT type 6 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1614928 Gbp7 guanylate binding protein 7 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20211216 MGI PMID:31964735 1614928 Gbp7 guanylate binding protein 7 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1614928 Gbp7 guanylate binding protein 7 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20211216 MGI PMID:31964735 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22284419 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:22284419 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:22284419 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22284419 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16713980 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:16713980 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20190207 MGI PMID:26880576 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:17723216 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16713980 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20150312 MGI PMID:24530055 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16785313 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:22284419 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:22284419 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:16785313 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:18178804 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22105994 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0006173 abnormal myeloid dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17723216 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18178804 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:17723216 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008548 abnormal circulating interferon level IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008548 abnormal circulating interferon level IAGP N RGD:5509061 20190117 MGI PMID:25008915 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008557 abnormal interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:21998457 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22105994 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:16785313 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:17723216 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:16785313 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:18178804 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:18439848 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:16785313 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008648 decreased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:18178804 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:22105994 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:18178804 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:16785313 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20190207 MGI PMID:26880576 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:22105994 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:16713980 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16785313 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0020943 increased susceptibility to Flaviviridae infection IAGP N RGD:5509061 20200430 MGI PMID:20140199 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:25981042 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0031039 decreased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:21998457 1614930 Mavs mitochondrial antiviral signaling protein gene MP:0031044 increased susceptibility to Flaviviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:20140199 1614932 Erfe erythroferrone gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:24880340 1614932 Erfe erythroferrone gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:24880340 1614932 Erfe erythroferrone gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:24880340 1614932 Erfe erythroferrone gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:24880340 1614932 Erfe erythroferrone gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:24880340 1614932 Erfe erythroferrone gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:24880340 1614932 Erfe erythroferrone gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:24880340 1614932 Erfe erythroferrone gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:24880340 1614932 Erfe erythroferrone gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:24880340 1614932 Erfe erythroferrone gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:24880340 1614933 Espnl espin-like gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20240321 MGI PMID:26926603 1614933 Espnl espin-like gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20240321 MGI PMID:26926603 1614933 Espnl espin-like gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1614933 Espnl espin-like gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20240523 MGI 1614933 Espnl espin-like gene MP:0006325 impaired hearing IAGP N RGD:5509061 20240321 MGI PMID:26926603 1614933 Espnl espin-like gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1614933 Espnl espin-like gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20240321 MGI PMID:26926603 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210128 MGI 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0000745 tremors IEA N RGD:5509061 20210128 MGI 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:19744960 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0001147 small testis IEA N RGD:5509061 20200402 MGI 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19744960 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19744960 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210520 MGI 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19744960 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:19744960 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:19744960 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210128 MGI 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:19744960 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210128 MGI 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20210128 MGI 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:19744960 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20141003 MGI PMID:19744960 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0008946 abnormal neuron number IAGP N RGD:5509061 20141003 MGI PMID:19744960 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19744960 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19744960 1614934 Gigyf2 GRB10 interacting GYF protein 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1614935 Gpr55 G protein-coupled receptor 55 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19805329 1614935 Gpr55 G protein-coupled receptor 55 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:19805329 1614935 Gpr55 G protein-coupled receptor 55 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1614935 Gpr55 G protein-coupled receptor 55 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20231207 MGI 1614935 Gpr55 G protein-coupled receptor 55 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:19805329 1614935 Gpr55 G protein-coupled receptor 55 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:19805329 1614935 Gpr55 G protein-coupled receptor 55 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:19805329 1614935 Gpr55 G protein-coupled receptor 55 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:19805329 1614935 Gpr55 G protein-coupled receptor 55 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19805329 1614935 Gpr55 G protein-coupled receptor 55 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20231207 MGI 1614935 Gpr55 G protein-coupled receptor 55 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:19805329 1614936 Ermp1 endoplasmic reticulum metallopeptidase 1 gene MP:0000111 cleft palate IEA N RGD:5509061 20170209 MGI 1614936 Ermp1 endoplasmic reticulum metallopeptidase 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 1614936 Ermp1 endoplasmic reticulum metallopeptidase 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20170209 MGI 1614936 Ermp1 endoplasmic reticulum metallopeptidase 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170209 MGI 1614936 Ermp1 endoplasmic reticulum metallopeptidase 1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 1614936 Ermp1 endoplasmic reticulum metallopeptidase 1 gene MP:0004158 right aortic arch IEA N RGD:5509061 20170209 MGI 1614936 Ermp1 endoplasmic reticulum metallopeptidase 1 gene MP:0005170 cleft upper lip IEA N RGD:5509061 20170209 MGI 1614936 Ermp1 endoplasmic reticulum metallopeptidase 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1614936 Ermp1 endoplasmic reticulum metallopeptidase 1 gene MP:0010466 vascular ring IEA N RGD:5509061 20170209 MGI 1614936 Ermp1 endoplasmic reticulum metallopeptidase 1 gene MP:0010488 abnormal left subclavian artery morphology IEA N RGD:5509061 20170209 MGI 1614936 Ermp1 endoplasmic reticulum metallopeptidase 1 gene MP:0011659 interrupted aortic arch, type b IEA N RGD:5509061 20170209 MGI 1614936 Ermp1 endoplasmic reticulum metallopeptidase 1 gene MP:0011670 double outlet right ventricle, noncommitted ventricular septal defect IEA N RGD:5509061 20170209 MGI 1614936 Ermp1 endoplasmic reticulum metallopeptidase 1 gene MP:0011954 shortened PQ interval IEA N RGD:5509061 20211021 MGI 1614937 Ric1 RAB6A GEF complex partner 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20141003 MGI 1614937 Ric1 RAB6A GEF complex partner 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20160804 MGI 1614937 Ric1 RAB6A GEF complex partner 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1614937 Ric1 RAB6A GEF complex partner 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1614937 Ric1 RAB6A GEF complex partner 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20160804 MGI 1614937 Ric1 RAB6A GEF complex partner 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20141003 MGI 1614937 Ric1 RAB6A GEF complex partner 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20141003 MGI 1614937 Ric1 RAB6A GEF complex partner 1 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1614937 Ric1 RAB6A GEF complex partner 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20141003 MGI 1614937 Ric1 RAB6A GEF complex partner 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20141003 MGI 1614937 Ric1 RAB6A GEF complex partner 1 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20141003 MGI 1614937 Ric1 RAB6A GEF complex partner 1 gene MP:0008211 decreased mature B cell number IEA N RGD:5509061 20141003 MGI 1614937 Ric1 RAB6A GEF complex partner 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20160804 MGI 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0001127 small ovary IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:30111536 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0001926 female infertility IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20200310 MGI PMID:30111536 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0009648 abnormal superovulation IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:30111536 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0011124 increased primary ovarian follicle number IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0012111 failure of morula compaction IAGP N RGD:5509061 20200310 MGI PMID:30111536 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0031382 absent secondary ovarian follicles IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614943 Dcaf13 DDB1 and CUL4 associated factor 13 gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220804 MGI PMID:30283081 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20210128 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20201022 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0001147 small testis IEA N RGD:5509061 20201022 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0001262 decreased body weight IEA N RGD:5509061 20201022 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210826 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0001925 male infertility IEA N RGD:5509061 20240523 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0002764 short tibia IEA N RGD:5509061 20230601 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20240523 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20240523 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20231207 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20240523 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0010936 decreased airway resistance IEA N RGD:5509061 20230601 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0011045 decreased lung elastance IEA N RGD:5509061 20231207 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210520 MGI 1614945 Marchf6 membrane associated ring-CH-type finger 6 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230119 MGI 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:11050238 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:11050238 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:11050238 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:11050238 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11050238 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230119 MGI 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:11050238 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0009951 abnormal olfactory bulb mitral cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0009964 abnormal cerebellum lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0010387 abnormal Bergmann glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20516067 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11050238 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1614946 Trio triple functional domain (PTPRF interacting) gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11050238 1614948 Eif4e1b eukaryotic translation initiation factor 4E family member 1B gene MP:0001926 female infertility IAGP N RGD:5509061 20231109 MGI PMID:36755190 1614948 Eif4e1b eukaryotic translation initiation factor 4E family member 1B gene MP:0001926 female infertility IAGP N RGD:5509061 20240905 MGI PMID:37257918 1614948 Eif4e1b eukaryotic translation initiation factor 4E family member 1B gene MP:0003718 maternal effect IAGP N RGD:5509061 20231109 MGI PMID:36755190 1614948 Eif4e1b eukaryotic translation initiation factor 4E family member 1B gene MP:0003718 maternal effect IAGP N RGD:5509061 20240905 MGI PMID:37257918 1614948 Eif4e1b eukaryotic translation initiation factor 4E family member 1B gene MP:0004832 enlarged ovary IAGP N RGD:5509061 20231109 MGI PMID:36755190 1614948 Eif4e1b eukaryotic translation initiation factor 4E family member 1B gene MP:0011124 increased primary ovarian follicle number IAGP N RGD:5509061 20231109 MGI PMID:36755190 1614948 Eif4e1b eukaryotic translation initiation factor 4E family member 1B gene MP:0011128 increased tertiary ovarian follicle number IAGP N RGD:5509061 20231109 MGI PMID:36755190 1614948 Eif4e1b eukaryotic translation initiation factor 4E family member 1B gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20231109 MGI PMID:36755190 1614950 Evi2b ecotropic viral integration site 2b gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1614950 Evi2b ecotropic viral integration site 2b gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1614954 Taok1 TAO kinase 1 gene MP:0000434 megacephaly IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20231207 MGI 1614954 Taok1 TAO kinase 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1614954 Taok1 TAO kinase 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1614954 Taok1 TAO kinase 1 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20231207 MGI 1614954 Taok1 TAO kinase 1 gene MP:0004144 hypotonia IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0004861 abnormal Raphe nucleus morphology IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 1614954 Taok1 TAO kinase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1614954 Taok1 TAO kinase 1 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0014416 decreased social novelty preference IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614954 Taok1 TAO kinase 1 gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20240516 MGI PMID:37656623 1614957 Myocd myocardin gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18188448 1614957 Myocd myocardin gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20200903 MGI PMID:31513549 1614957 Myocd myocardin gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20200903 MGI PMID:31513549 1614957 Myocd myocardin gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:18188448 1614957 Myocd myocardin gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12867591 1614957 Myocd myocardin gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:12867591 1614957 Myocd myocardin gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:12867591 1614957 Myocd myocardin gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0002083 premature death IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17940050 1614957 Myocd myocardin gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:18188448 1614957 Myocd myocardin gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20200903 MGI PMID:31513549 1614957 Myocd myocardin gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12867591 1614957 Myocd myocardin gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20150226 MGI PMID:25174608 1614957 Myocd myocardin gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12867591 1614957 Myocd myocardin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:12867591 1614957 Myocd myocardin gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12867591 1614957 Myocd myocardin gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:18188448 1614957 Myocd myocardin gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18188448 1614957 Myocd myocardin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200903 MGI PMID:31513549 1614957 Myocd myocardin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20150226 MGI PMID:25174608 1614957 Myocd myocardin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12867591 1614957 Myocd myocardin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18188448 1614957 Myocd myocardin gene MP:0011774 abnormal urinary bladder detrusor smooth muscle morphology IAGP N RGD:5509061 20200903 MGI PMID:31513549 1614957 Myocd myocardin gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0012270 cardiac edema IAGP N RGD:5509061 20150226 MGI PMID:25174608 1614957 Myocd myocardin gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20170831 MGI PMID:19850880 1614957 Myocd myocardin gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:19850880 1614959 Tmem51 transmembrane protein 51 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20221215 MGI 1614959 Tmem51 transmembrane protein 51 gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 1614959 Tmem51 transmembrane protein 51 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1614959 Tmem51 transmembrane protein 51 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20181227 MGI 1614959 Tmem51 transmembrane protein 51 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 1614959 Tmem51 transmembrane protein 51 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1614959 Tmem51 transmembrane protein 51 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20181227 MGI 1614959 Tmem51 transmembrane protein 51 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1614967 Bnip5 BCL2 interacting protein 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1614967 Bnip5 BCL2 interacting protein 5 gene MP:0000692 small spleen IEA N RGD:5509061 20210128 MGI 1614967 Bnip5 BCL2 interacting protein 5 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1614968 Smagp small cell adhesion glycoprotein gene MP:0003960 increased lean body mass IEA N RGD:5509061 20190502 MGI 1614969 Usf3 upstream transcription factor family member 3 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1614969 Usf3 upstream transcription factor family member 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0009511 distended stomach IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0010802 abnormal intestinal enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0014077 ectopic Paneth cells IAGP N RGD:5509061 20160310 MGI PMID:22510880 1614973 Nrbp1 nuclear receptor binding protein 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:22510880 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:15172687 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18079413 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:18079413 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:18079413 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15172687 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0004055 heart atrium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15172687 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:18079413 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:18079413 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20141003 MGI PMID:18079413 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15172687 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:15172687 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15172687 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15172687 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18079413 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0011392 increased fetal cardiomyocyte apoptosis IAGP N RGD:5509061 20240321 MGI PMID:15172687 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0031607 abnormal fetal cardiomyocyte mitochondrial morphology IAGP N RGD:5509061 20240321 MGI PMID:15172687 1614974 Hexim1 hexamethylene bis-acetamide inducible 1 gene MP:0031611 decreased fetal cardiomyocyte number IAGP N RGD:5509061 20240321 MGI PMID:15172687 1614978 Derl2 Der1-like domain family, member 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21220515 1614978 Derl2 Der1-like domain family, member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614982 Npnt nephronectin gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:17537792 1614982 Npnt nephronectin gene MP:0000520 absent kidney IAGP N RGD:5509061 20211202 MGI PMID:34049960 1614982 Npnt nephronectin gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:17537792 1614982 Npnt nephronectin gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20211202 MGI PMID:34049960 1614982 Npnt nephronectin gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17537792 1614982 Npnt nephronectin gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:17537792 1614982 Npnt nephronectin gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:17537792 1614982 Npnt nephronectin gene MP:0003722 absent ureter IAGP N RGD:5509061 20211202 MGI PMID:34049960 1614982 Npnt nephronectin gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17537792 1614982 Npnt nephronectin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20211202 MGI PMID:34049960 1614985 Shroom2 shroom family member 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 1614985 Shroom2 shroom family member 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1614985 Shroom2 shroom family member 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1614985 Shroom2 shroom family member 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 1614988 Pp2d1 protein phosphatase 2C-like domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210506 MGI PMID:32814578 1614989 Cox6b1 cytochrome c oxidase, subunit 6B1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1614989 Cox6b1 cytochrome c oxidase, subunit 6B1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200310 MGI 1614989 Cox6b1 cytochrome c oxidase, subunit 6B1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20200310 MGI 1614989 Cox6b1 cytochrome c oxidase, subunit 6B1 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20220811 MGI 1614989 Cox6b1 cytochrome c oxidase, subunit 6B1 gene MP:0004357 long tibia IEA N RGD:5509061 20240523 MGI 1614989 Cox6b1 cytochrome c oxidase, subunit 6B1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1614989 Cox6b1 cytochrome c oxidase, subunit 6B1 gene MP:0005313 absent adrenal gland IEA N RGD:5509061 20200310 MGI 1614989 Cox6b1 cytochrome c oxidase, subunit 6B1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200310 MGI 1614990 Fbxw17 F-box and WD-40 domain protein 17 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1614993 Aldh1l1 aldehyde dehydrogenase 1 family, member L1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20200310 MGI 1614993 Aldh1l1 aldehyde dehydrogenase 1 family, member L1 gene MP:0001304 cataract IEA N RGD:5509061 20200310 MGI 1614993 Aldh1l1 aldehyde dehydrogenase 1 family, member L1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20200310 MGI PMID:31624291 1614993 Aldh1l1 aldehyde dehydrogenase 1 family, member L1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 1614993 Aldh1l1 aldehyde dehydrogenase 1 family, member L1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1614993 Aldh1l1 aldehyde dehydrogenase 1 family, member L1 gene MP:0011230 abnormal folic acid level IAGP N RGD:5509061 20200310 MGI PMID:31624291 1614993 Aldh1l1 aldehyde dehydrogenase 1 family, member L1 gene MP:0030659 decreased glycine level IAGP N RGD:5509061 20200310 MGI PMID:31624291 1614993 Aldh1l1 aldehyde dehydrogenase 1 family, member L1 gene MP:0030691 increased serine level IAGP N RGD:5509061 20200310 MGI PMID:31624291 1614994 Rapgef1 Rap guanine nucleotide exchange factor (GEF) 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1614994 Rapgef1 Rap guanine nucleotide exchange factor (GEF) 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:12466202 1614994 Rapgef1 Rap guanine nucleotide exchange factor (GEF) 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12466202 1614994 Rapgef1 Rap guanine nucleotide exchange factor (GEF) 1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:12466202 1614994 Rapgef1 Rap guanine nucleotide exchange factor (GEF) 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:12466202 1614994 Rapgef1 Rap guanine nucleotide exchange factor (GEF) 1 gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12466202 1614994 Rapgef1 Rap guanine nucleotide exchange factor (GEF) 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16858399 1614994 Rapgef1 Rap guanine nucleotide exchange factor (GEF) 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12466202 1614994 Rapgef1 Rap guanine nucleotide exchange factor (GEF) 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12466202 1614994 Rapgef1 Rap guanine nucleotide exchange factor (GEF) 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11432821 1614994 Rapgef1 Rap guanine nucleotide exchange factor (GEF) 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12466202 1614994 Rapgef1 Rap guanine nucleotide exchange factor (GEF) 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1614994 Rapgef1 Rap guanine nucleotide exchange factor (GEF) 1 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:12466202 1614995 Mrpl41 mitochondrial ribosomal protein L41 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210520 MGI 1614995 Mrpl41 mitochondrial ribosomal protein L41 gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20111116 MGI 1614995 Mrpl41 mitochondrial ribosomal protein L41 gene MP:0001695 abnormal gastrulation IEA N RGD:5509061 20241010 MGI 1614995 Mrpl41 mitochondrial ribosomal protein L41 gene MP:0002230 abnormal primitive streak formation IEA N RGD:5509061 20241010 MGI 1614995 Mrpl41 mitochondrial ribosomal protein L41 gene MP:0002582 disorganized extraembryonic tissue IEA N RGD:5509061 20241010 MGI 1614995 Mrpl41 mitochondrial ribosomal protein L41 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20241010 MGI 1614995 Mrpl41 mitochondrial ribosomal protein L41 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241010 MGI 1614995 Mrpl41 mitochondrial ribosomal protein L41 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1614995 Mrpl41 mitochondrial ribosomal protein L41 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1615000 Zfp692 zinc finger protein 692 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1615001 Tra2a transformer 2 alpha gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20210128 MGI 1615001 Tra2a transformer 2 alpha gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11165478 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8643689 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615004 Ankrd17 ankyrin repeat domain 17 gene MP:0011264 abnormal cardiac mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:19619540 1615005 Egfl8 EGF-like domain 8 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1615005 Egfl8 EGF-like domain 8 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20170105 MGI 1615005 Egfl8 EGF-like domain 8 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20170105 MGI 1615005 Egfl8 EGF-like domain 8 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170413 MGI 1615005 Egfl8 EGF-like domain 8 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170105 MGI 1615005 Egfl8 EGF-like domain 8 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20170105 MGI 1615008 Lbh limb-bud and heart gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:23495064 1615008 Lbh limb-bud and heart gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23495064 1615008 Lbh limb-bud and heart gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23495064 1615008 Lbh limb-bud and heart gene MP:0003344 mammary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23495064 1615008 Lbh limb-bud and heart gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:23495064 1615008 Lbh limb-bud and heart gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:23495064 1615008 Lbh limb-bud and heart gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:23495064 1615008 Lbh limb-bud and heart gene MP:0012075 impaired mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:23495064 1615016 Esco1 establishment of sister chromatid cohesion N-acetyltransferase 1 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 1615016 Esco1 establishment of sister chromatid cohesion N-acetyltransferase 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1615016 Esco1 establishment of sister chromatid cohesion N-acetyltransferase 1 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1615016 Esco1 establishment of sister chromatid cohesion N-acetyltransferase 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20211216 MGI PMID:32555289 1615016 Esco1 establishment of sister chromatid cohesion N-acetyltransferase 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1615016 Esco1 establishment of sister chromatid cohesion N-acetyltransferase 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160804 MGI 1615016 Esco1 establishment of sister chromatid cohesion N-acetyltransferase 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160804 MGI 1615016 Esco1 establishment of sister chromatid cohesion N-acetyltransferase 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1615019 Mib2 mindbomb E3 ubiquitin protein ligase 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:17987667 1615019 Mib2 mindbomb E3 ubiquitin protein ligase 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20200310 MGI 1615019 Mib2 mindbomb E3 ubiquitin protein ligase 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20200310 MGI 1615019 Mib2 mindbomb E3 ubiquitin protein ligase 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200310 MGI 1615019 Mib2 mindbomb E3 ubiquitin protein ligase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:18043734 1615019 Mib2 mindbomb E3 ubiquitin protein ligase 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20200310 MGI 1615019 Mib2 mindbomb E3 ubiquitin protein ligase 2 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20200310 MGI 1615019 Mib2 mindbomb E3 ubiquitin protein ligase 2 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20200310 MGI PMID:18043734 1615019 Mib2 mindbomb E3 ubiquitin protein ligase 2 gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20200310 MGI 1615019 Mib2 mindbomb E3 ubiquitin protein ligase 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200310 MGI 1615019 Mib2 mindbomb E3 ubiquitin protein ligase 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200310 MGI 1615019 Mib2 mindbomb E3 ubiquitin protein ligase 2 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17987667 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200310 MGI 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0001148 enlarged testis IEA N RGD:5509061 20200310 MGI 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200310 MGI 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20200310 MGI 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20200310 MGI PMID:24828040 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20200310 MGI 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0005283 increased unsaturated fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0005285 decreased unsaturated fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20200310 MGI PMID:24828040 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0009392 retina gliosis IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0010762 abnormal microglial cell activation IAGP N RGD:5509061 20200310 MGI PMID:27008858 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20200310 MGI PMID:23209793 1615020 Mfsd2a MFSD2 lysolipid transporter A, lysophospholipid gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:24828040 1615021 Spatc1l spermatogenesis and centriole associated 1 like gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20181018 MGI PMID:30026308 1615021 Spatc1l spermatogenesis and centriole associated 1 like gene MP:0001925 male infertility IAGP N RGD:5509061 20181018 MGI PMID:30026308 1615021 Spatc1l spermatogenesis and centriole associated 1 like gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20221215 MGI 1615021 Spatc1l spermatogenesis and centriole associated 1 like gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20181018 MGI PMID:30026308 1615021 Spatc1l spermatogenesis and centriole associated 1 like gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20181018 MGI PMID:30026308 1615021 Spatc1l spermatogenesis and centriole associated 1 like gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20181018 MGI PMID:30026308 1615021 Spatc1l spermatogenesis and centriole associated 1 like gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20181018 MGI PMID:30026308 1615021 Spatc1l spermatogenesis and centriole associated 1 like gene MP:0009234 absent sperm head IAGP N RGD:5509061 20181018 MGI PMID:30026308 1615022 Rbmxl2 RNA binding motif protein, X-linked-like 2 gene MP:0001147 small testis IAGP N RGD:5509061 20191107 MGI PMID:30674417 1615022 Rbmxl2 RNA binding motif protein, X-linked-like 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20191107 MGI PMID:30674417 1615022 Rbmxl2 RNA binding motif protein, X-linked-like 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20191107 MGI PMID:30674417 1615022 Rbmxl2 RNA binding motif protein, X-linked-like 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20191107 MGI PMID:30674417 1615022 Rbmxl2 RNA binding motif protein, X-linked-like 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20191107 MGI PMID:30674417 1615022 Rbmxl2 RNA binding motif protein, X-linked-like 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20191107 MGI PMID:30674417 1615022 Rbmxl2 RNA binding motif protein, X-linked-like 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20191107 MGI PMID:30674417 1615023 Rflnb refilin B gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0000139 absent vertebral transverse processes IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0000160 kyphosis IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0000161 scoliosis IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0001255 decreased body height IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0001258 decreased body length IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0001265 decreased body size IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15661651 1615023 Rflnb refilin B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151112 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0002764 short tibia IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0003109 short femur IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0004600 abnormal vertebral transverse process morphology IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0004606 absent vertebral spinous process IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0004610 small vertebrae IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0004682 small intervertebral disk IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0004684 intervertebral disk degeneration IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0005227 abnormal vertebral body development IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0006392 abnormal nucleus pulposus morphology IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20151008 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20171221 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0014107 premature chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:24436304 1615023 Rflnb refilin B gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:24436304 1615024 Ccdc6 coiled-coil domain containing 6 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20210617 MGI PMID:25970781 1615024 Ccdc6 coiled-coil domain containing 6 gene MP:0003498 thyroid gland hyperplasia IAGP N RGD:5509061 20210617 MGI PMID:25970781 1615024 Ccdc6 coiled-coil domain containing 6 gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20210617 MGI PMID:25970781 1615024 Ccdc6 coiled-coil domain containing 6 gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20210617 MGI PMID:25970781 1615024 Ccdc6 coiled-coil domain containing 6 gene MP:0005474 increased triiodothyronine level IAGP N RGD:5509061 20210617 MGI PMID:25970781 1615024 Ccdc6 coiled-coil domain containing 6 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20210617 MGI PMID:25970781 1615024 Ccdc6 coiled-coil domain containing 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615024 Ccdc6 coiled-coil domain containing 6 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20210617 MGI PMID:25970781 1615024 Ccdc6 coiled-coil domain containing 6 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20210617 MGI PMID:25970781 1615024 Ccdc6 coiled-coil domain containing 6 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20210617 MGI PMID:25970781 1615026 Plet1 placenta expressed transcript 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20191114 MGI PMID:29070673 1615026 Plet1 placenta expressed transcript 1 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1615026 Plet1 placenta expressed transcript 1 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20191114 MGI PMID:29070673 1615026 Plet1 placenta expressed transcript 1 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20211021 MGI 1615026 Plet1 placenta expressed transcript 1 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20210617 MGI PMID:30537036 1615026 Plet1 placenta expressed transcript 1 gene MP:0008125 abnormal dendritic cell number IAGP N RGD:5509061 20210617 MGI PMID:30537036 1615026 Plet1 placenta expressed transcript 1 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20210617 MGI PMID:30537036 1615026 Plet1 placenta expressed transcript 1 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20191114 MGI PMID:29070673 1615026 Plet1 placenta expressed transcript 1 gene MP:0020349 abnormal dendritic cell migration IAGP N RGD:5509061 20210617 MGI PMID:30537036 1615038 Rnf19b ring finger protein 19B gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200514 MGI 1615038 Rnf19b ring finger protein 19B gene MP:0000274 enlarged heart IEA N RGD:5509061 20200514 MGI 1615038 Rnf19b ring finger protein 19B gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20200310 MGI PMID:19915045 1615038 Rnf19b ring finger protein 19B gene MP:0001314 cornea opacity IEA N RGD:5509061 20240523 MGI 1615038 Rnf19b ring finger protein 19B gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1615038 Rnf19b ring finger protein 19B gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20240523 MGI 1615038 Rnf19b ring finger protein 19B gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:19915045 1615038 Rnf19b ring finger protein 19B gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1615038 Rnf19b ring finger protein 19B gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20200310 MGI PMID:19915045 1615038 Rnf19b ring finger protein 19B gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:19915045 1615038 Rnf19b ring finger protein 19B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1615039 Cep128 centrosomal protein 128 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220428 MGI PMID:35296684 1615039 Cep128 centrosomal protein 128 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20231207 MGI 1615039 Cep128 centrosomal protein 128 gene MP:0001925 male infertility IAGP N RGD:5509061 20220428 MGI PMID:35296684 1615039 Cep128 centrosomal protein 128 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220428 MGI PMID:35296684 1615039 Cep128 centrosomal protein 128 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220428 MGI PMID:35296684 1615039 Cep128 centrosomal protein 128 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20220428 MGI PMID:35296684 1615039 Cep128 centrosomal protein 128 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220428 MGI PMID:35296684 1615039 Cep128 centrosomal protein 128 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220428 MGI PMID:35296684 1615039 Cep128 centrosomal protein 128 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20220428 MGI PMID:35296684 1615039 Cep128 centrosomal protein 128 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220428 MGI PMID:35296684 1615039 Cep128 centrosomal protein 128 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220428 MGI PMID:35296684 1615039 Cep128 centrosomal protein 128 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220428 MGI PMID:35296684 1615041 Spaca6 sperm acrosome associated 6 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20150129 MGI PMID:24275887 1615041 Spaca6 sperm acrosome associated 6 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20210520 MGI PMID:33871360 1615041 Spaca6 sperm acrosome associated 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20150129 MGI PMID:24275887 1615041 Spaca6 sperm acrosome associated 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20200716 MGI PMID:32393636 1615041 Spaca6 sperm acrosome associated 6 gene MP:0031010 failure of sperm-egg fusion IAGP N RGD:5509061 20200716 MGI PMID:32393636 1615046 Fam151b family with sequence similarity 151, member B gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1615046 Fam151b family with sequence similarity 151, member B gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1615046 Fam151b family with sequence similarity 151, member B gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20200730 MGI PMID:31949211 1615046 Fam151b family with sequence similarity 151, member B gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20200730 MGI PMID:31949211 1615046 Fam151b family with sequence similarity 151, member B gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20200730 MGI PMID:31949211 1615046 Fam151b family with sequence similarity 151, member B gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20200730 MGI PMID:31949211 1615046 Fam151b family with sequence similarity 151, member B gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200730 MGI PMID:31949211 1615046 Fam151b family with sequence similarity 151, member B gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200730 MGI PMID:31949211 1615046 Fam151b family with sequence similarity 151, member B gene MP:0020816 decreased photoreceptor outer segment number IAGP N RGD:5509061 20200730 MGI PMID:31949211 1615049 Lime1 Lck interacting transmembrane adaptor 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20240523 MGI 1615049 Lime1 Lck interacting transmembrane adaptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21915273 1615049 Lime1 Lck interacting transmembrane adaptor 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:17918199 1615049 Lime1 Lck interacting transmembrane adaptor 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17918199 1615049 Lime1 Lck interacting transmembrane adaptor 1 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17918199 1615051 Skida1 SKI/DACH domain containing 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1615051 Skida1 SKI/DACH domain containing 1 gene MP:0000692 small spleen IEA N RGD:5509061 20160811 MGI 1615051 Skida1 SKI/DACH domain containing 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20160811 MGI 1615051 Skida1 SKI/DACH domain containing 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20160811 MGI 1615051 Skida1 SKI/DACH domain containing 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 1615051 Skida1 SKI/DACH domain containing 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1615051 Skida1 SKI/DACH domain containing 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1615051 Skida1 SKI/DACH domain containing 1 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20160114 MGI 1615051 Skida1 SKI/DACH domain containing 1 gene MP:0005477 increased circulating thyroxine level IEA N RGD:5509061 20211021 MGI 1615051 Skida1 SKI/DACH domain containing 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20150108 MGI 1615051 Skida1 SKI/DACH domain containing 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20150108 MGI 1615051 Skida1 SKI/DACH domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20160114 MGI 1615056 Mex3a mex3 RNA binding family member A gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20200611 MGI PMID:32052574 1615056 Mex3a mex3 RNA binding family member A gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20200611 MGI PMID:32052574 1615056 Mex3a mex3 RNA binding family member A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200611 MGI PMID:32052574 1615056 Mex3a mex3 RNA binding family member A gene MP:0001263 weight loss IAGP N RGD:5509061 20200611 MGI PMID:32052574 1615056 Mex3a mex3 RNA binding family member A gene MP:0001265 decreased body size IAGP N RGD:5509061 20200611 MGI PMID:32052574 1615056 Mex3a mex3 RNA binding family member A gene MP:0001429 dehydration IAGP N RGD:5509061 20200611 MGI PMID:32052574 1615056 Mex3a mex3 RNA binding family member A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200611 MGI PMID:32052574 1615056 Mex3a mex3 RNA binding family member A gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200611 MGI PMID:32052574 1615056 Mex3a mex3 RNA binding family member A gene MP:0005202 lethargy IAGP N RGD:5509061 20200611 MGI PMID:32052574 1615056 Mex3a mex3 RNA binding family member A gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20200611 MGI PMID:32052574 1615056 Mex3a mex3 RNA binding family member A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200611 MGI PMID:32052574 1615056 Mex3a mex3 RNA binding family member A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200611 MGI PMID:32052574 1615056 Mex3a mex3 RNA binding family member A gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20200611 MGI PMID:32052574 1615056 Mex3a mex3 RNA binding family member A gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20200611 MGI PMID:32052574 1615056 Mex3a mex3 RNA binding family member A gene MP:0014201 abnormal intestinal epithelium physiology IAGP N RGD:5509061 20200611 MGI PMID:32052574 1615056 Mex3a mex3 RNA binding family member A gene MP:0014353 abnormal gastrointestinal brush cell morphology IAGP N RGD:5509061 20240104 MGI PMID:32052574 1615057 Lins1 lines homolog 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1615057 Lins1 lines homolog 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1615059 Cdcp3 CUB domain containing protein 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1615059 Cdcp3 CUB domain containing protein 3 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20201022 MGI 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18437205 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:23150520 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:5098070 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:5098070 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:5098070 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:5098070 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20170105 MGI 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:23150520 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18437205 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:15200409 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18437205 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:5098070 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:18437205 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:5098070 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0003158 dysphagia IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16120817 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23150520 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:16120817 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:23150520 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:5098070 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0004537 abnormal palatine bone horizontal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20170105 MGI 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:5098070 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:5098070 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18437205 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16120817 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:23150520 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:5098070 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:23150520 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16120817 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:23150520 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16120817 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23150520 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18437205 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:15200409 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:16120817 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0009718 absent Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0010008 abnormal Purkinje cell migration IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:18437205 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:18437205 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:23150520 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:18437205 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:23150520 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:18437205 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18437205 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:16120817 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:5098070 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16120817 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:5098070 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:15200409 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:18437205 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:23150520 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0011413 colorless urine IAGP N RGD:5509061 20141003 MGI PMID:5098070 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0011498 abnormal glomerular capsule parietal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16120817 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0011534 granular kidney IAGP N RGD:5509061 20141003 MGI PMID:5098070 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20141003 MGI PMID:23150520 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20161117 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0012090 midbrain hypoplasia IAGP N RGD:5509061 20161117 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20160304 MGI PMID:18437205 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0014388 decreased hepatocyte mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:23150520 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0020388 decreased radial glial cell number IAGP N RGD:5509061 20161117 MGI PMID:21871565 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1615065 Pdss2 prenyl (solanesyl) diphosphate synthase, subunit 2 gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20190711 MGI PMID:23150520 1615067 Ano9 anoctamin 9 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20240229 MGI PMID:36330924 1615067 Ano9 anoctamin 9 gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20240229 MGI PMID:36330924 1615067 Ano9 anoctamin 9 gene MP:0020852 abnormal olfactory behavior IAGP N RGD:5509061 20240229 MGI PMID:36330924 1615068 Rassf8 Ras association (RalGDS/AF-6) domain family (N-terminal) member 8 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200310 MGI 1615068 Rassf8 Ras association (RalGDS/AF-6) domain family (N-terminal) member 8 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200310 MGI 1615068 Rassf8 Ras association (RalGDS/AF-6) domain family (N-terminal) member 8 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20200310 MGI 1615068 Rassf8 Ras association (RalGDS/AF-6) domain family (N-terminal) member 8 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200310 MGI 1615068 Rassf8 Ras association (RalGDS/AF-6) domain family (N-terminal) member 8 gene MP:0001147 small testis IEA N RGD:5509061 20200310 MGI 1615068 Rassf8 Ras association (RalGDS/AF-6) domain family (N-terminal) member 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1615068 Rassf8 Ras association (RalGDS/AF-6) domain family (N-terminal) member 8 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1615069 Fsip1 fibrous sheath-interacting protein 1 gene MP:0001925 male infertility IEA N RGD:5509061 20231207 MGI 1615069 Fsip1 fibrous sheath-interacting protein 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20240627 MGI PMID:33901807 1615069 Fsip1 fibrous sheath-interacting protein 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20240627 MGI PMID:33901807 1615069 Fsip1 fibrous sheath-interacting protein 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240627 MGI PMID:33901807 1615069 Fsip1 fibrous sheath-interacting protein 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20240627 MGI PMID:33901807 1615069 Fsip1 fibrous sheath-interacting protein 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20240627 MGI PMID:33901807 1615069 Fsip1 fibrous sheath-interacting protein 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20240627 MGI PMID:33901807 1615069 Fsip1 fibrous sheath-interacting protein 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240627 MGI PMID:33901807 1615069 Fsip1 fibrous sheath-interacting protein 1 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20240627 MGI PMID:33901807 1615069 Fsip1 fibrous sheath-interacting protein 1 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20240627 MGI PMID:33901807 1615071 Rnf148 ring finger protein 148 gene MP:0000160 kyphosis IEA N RGD:5509061 20210128 MGI 1615071 Rnf148 ring finger protein 148 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1615071 Rnf148 ring finger protein 148 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1615071 Rnf148 ring finger protein 148 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1615071 Rnf148 ring finger protein 148 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1615071 Rnf148 ring finger protein 148 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1615071 Rnf148 ring finger protein 148 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20241017 MGI PMID:35831855 1615071 Rnf148 ring finger protein 148 gene MP:0002286 cryptorchism IEA N RGD:5509061 20210128 MGI 1615071 Rnf148 ring finger protein 148 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20241017 MGI PMID:35831855 1615071 Rnf148 ring finger protein 148 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20210128 MGI 1615071 Rnf148 ring finger protein 148 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220519 MGI 1615071 Rnf148 ring finger protein 148 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220519 MGI 1615071 Rnf148 ring finger protein 148 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20241017 MGI PMID:35831855 1615071 Rnf148 ring finger protein 148 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20241017 MGI PMID:35831855 1615071 Rnf148 ring finger protein 148 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20241017 MGI PMID:35831855 1615071 Rnf148 ring finger protein 148 gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20241017 MGI PMID:35831855 1615071 Rnf148 ring finger protein 148 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20241017 MGI PMID:35831855 1615071 Rnf148 ring finger protein 148 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220519 MGI 1615072 Metrn meteorin, glial cell differentiation regulator gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230601 MGI 1615072 Metrn meteorin, glial cell differentiation regulator gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1615072 Metrn meteorin, glial cell differentiation regulator gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1615072 Metrn meteorin, glial cell differentiation regulator gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1615072 Metrn meteorin, glial cell differentiation regulator gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20200310 MGI PMID:24558432 1615072 Metrn meteorin, glial cell differentiation regulator gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20200310 MGI PMID:24558432 1615072 Metrn meteorin, glial cell differentiation regulator gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:24558432 1615072 Metrn meteorin, glial cell differentiation regulator gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1615072 Metrn meteorin, glial cell differentiation regulator gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20200310 MGI PMID:24558432 1615072 Metrn meteorin, glial cell differentiation regulator gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24558432 1615075 H1f7 H1.7 linker histone gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:16055721 1615075 H1f7 H1.7 linker histone gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16055721 1615075 H1f7 H1.7 linker histone gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15710904 1615075 H1f7 H1.7 linker histone gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16055721 1615075 H1f7 H1.7 linker histone gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15710904 1615075 H1f7 H1.7 linker histone gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15710904 1615075 H1f7 H1.7 linker histone gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16055721 1615075 H1f7 H1.7 linker histone gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15710904 1615075 H1f7 H1.7 linker histone gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:16055721 1615075 H1f7 H1.7 linker histone gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16055721 1615075 H1f7 H1.7 linker histone gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:15710904 1615075 H1f7 H1.7 linker histone gene MP:0009231 detached acrosome IAGP N RGD:5509061 20141003 MGI PMID:15710904 1615075 H1f7 H1.7 linker histone gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15710904 1615076 Spata3 spermatogenesis associated 3 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20210603 MGI PMID:33669425 1615076 Spata3 spermatogenesis associated 3 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1615076 Spata3 spermatogenesis associated 3 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210603 MGI PMID:33669425 1615076 Spata3 spermatogenesis associated 3 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20210603 MGI PMID:33669425 1615078 Gpr15lg G protein coupled receptor 15 ligand gene MP:0008500 increased IgG2a level IEA N RGD:5509061 20170323 MGI 1615079 Dancr differentiation antagonizing non-protein coding RNA gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20221124 MGI PMID:36183859 1615079 Dancr differentiation antagonizing non-protein coding RNA gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20221124 MGI PMID:36183859 1615080 Tspo2 translocator protein 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20201224 MGI PMID:32358067 1615080 Tspo2 translocator protein 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20201224 MGI PMID:32358067 1615080 Tspo2 translocator protein 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20201224 MGI PMID:32358067 1615080 Tspo2 translocator protein 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20201224 MGI PMID:32358067 1615080 Tspo2 translocator protein 2 gene MP:0011176 abnormal erythroblast morphology IAGP N RGD:5509061 20201224 MGI PMID:32358067 1615080 Tspo2 translocator protein 2 gene MP:0012393 increased erythrocyte sodium:potassium-exchanging ATPase activity IAGP N RGD:5509061 20201224 MGI PMID:32358067 1615086 Rgmb repulsive guidance molecule family member B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21187450 1615087 Ubr3 ubiquitin protein ligase E3 component n-recognin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17462990 1615087 Ubr3 ubiquitin protein ligase E3 component n-recognin 3 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:17462990 1615087 Ubr3 ubiquitin protein ligase E3 component n-recognin 3 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:17462990 1615087 Ubr3 ubiquitin protein ligase E3 component n-recognin 3 gene MP:0004512 anosmia IAGP N RGD:5509061 20141003 MGI PMID:17462990 1615087 Ubr3 ubiquitin protein ligase E3 component n-recognin 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17462990 1615087 Ubr3 ubiquitin protein ligase E3 component n-recognin 3 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17462990 1615089 Ms4a6d membrane-spanning 4-domains, subfamily A, member 6D gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20240418 MGI PMID:37429063 1615091 Cdhr3 cadherin-related family member 3 gene MP:0000745 tremors IEA N RGD:5509061 20240523 MGI 1615091 Cdhr3 cadherin-related family member 3 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20200310 MGI 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20200310 MGI 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201210 MGI PMID:32579589 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0001297 microphthalmia IEA N RGD:5509061 20200310 MGI 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0001304 cataract IAGP N RGD:5509061 20201210 MGI PMID:32579589 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20201210 MGI PMID:32579589 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0002001 blindness IAGP N RGD:5509061 20201210 MGI PMID:32579589 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200310 MGI 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20201210 MGI PMID:32579589 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20201210 MGI PMID:32579589 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20201210 MGI PMID:32579589 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0004222 iris synechia IAGP N RGD:5509061 20201210 MGI PMID:32579589 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0005194 abnormal anterior uvea morphology IAGP N RGD:5509061 20201210 MGI PMID:32579589 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20201210 MGI PMID:32579589 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20201210 MGI PMID:32579589 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20201210 MGI PMID:32579589 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0009287 decreased abdominal fat pad weight IAGP N RGD:5509061 20201210 MGI PMID:32579589 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0009709 hydrometra IEA N RGD:5509061 20200310 MGI 1615093 Abhd11 abhydrolase domain containing 11 gene MP:0014476 abnormal feces lipid level IAGP N RGD:5509061 20240704 MGI PMID:32579589 1615095 Tmem219 transmembrane protein 219 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20170713 MGI PMID:27629921 1615095 Tmem219 transmembrane protein 219 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20170713 MGI PMID:27629921 1615095 Tmem219 transmembrane protein 219 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20170713 MGI PMID:27629921 1615095 Tmem219 transmembrane protein 219 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20170713 MGI PMID:27629921 1615095 Tmem219 transmembrane protein 219 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20170713 MGI PMID:27629921 1615095 Tmem219 transmembrane protein 219 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20170713 MGI PMID:27629921 1615095 Tmem219 transmembrane protein 219 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20170713 MGI PMID:27629921 1615095 Tmem219 transmembrane protein 219 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20170713 MGI PMID:27629921 1615095 Tmem219 transmembrane protein 219 gene MP:0008837 increased transforming growth factor beta level IAGP N RGD:5509061 20170713 MGI PMID:27629921 1615095 Tmem219 transmembrane protein 219 gene MP:0008838 decreased transforming growth factor beta level IAGP N RGD:5509061 20170713 MGI PMID:27629921 1615095 Tmem219 transmembrane protein 219 gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20170713 MGI PMID:27629921 1615095 Tmem219 transmembrane protein 219 gene MP:0030002 increased lung apoptosis IAGP N RGD:5509061 20170713 MGI PMID:27629921 1615097 Acss1 acyl-CoA synthetase short-chain family member 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20200310 MGI PMID:19187775 1615097 Acss1 acyl-CoA synthetase short-chain family member 1 gene MP:0001553 abnormal circulating free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:19187775 1615097 Acss1 acyl-CoA synthetase short-chain family member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:19187775 1615097 Acss1 acyl-CoA synthetase short-chain family member 1 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20200310 MGI PMID:19187775 1615097 Acss1 acyl-CoA synthetase short-chain family member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19187775 1615097 Acss1 acyl-CoA synthetase short-chain family member 1 gene MP:0002332 abnormal exercise endurance IAGP N RGD:5509061 20200310 MGI PMID:19187775 1615097 Acss1 acyl-CoA synthetase short-chain family member 1 gene MP:0002865 increased growth rate IAGP N RGD:5509061 20200310 MGI PMID:19187775 1615097 Acss1 acyl-CoA synthetase short-chain family member 1 gene MP:0003860 abnormal carbon dioxide level IAGP N RGD:5509061 20200310 MGI PMID:19187775 1615097 Acss1 acyl-CoA synthetase short-chain family member 1 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20200310 MGI PMID:19187775 1615097 Acss1 acyl-CoA synthetase short-chain family member 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:19187775 1615097 Acss1 acyl-CoA synthetase short-chain family member 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20200310 MGI PMID:19187775 1615097 Acss1 acyl-CoA synthetase short-chain family member 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20200310 MGI PMID:19187775 1615097 Acss1 acyl-CoA synthetase short-chain family member 1 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20200310 MGI PMID:19187775 1615097 Acss1 acyl-CoA synthetase short-chain family member 1 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20200310 MGI PMID:19187775 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220811 MGI 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0000599 enlarged liver IEA N RGD:5509061 20220811 MGI 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20191219 MGI PMID:24713655 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20210304 MGI PMID:30853298 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20210304 MGI PMID:30853298 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0001025 abnormal sympathetic neuron morphology IAGP N RGD:5509061 20210304 MGI PMID:30853298 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220811 MGI 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0001148 enlarged testis IEA N RGD:5509061 20220811 MGI 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20210304 MGI PMID:30853298 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20191219 MGI PMID:24713655 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20191219 MGI PMID:24713655 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0009284 abnormal sympathetic neuron innervation pattern IAGP N RGD:5509061 20210304 MGI PMID:30853298 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20191219 MGI PMID:24713655 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20191219 MGI PMID:24713655 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0010238 increased skeletal muscle weight IAGP N RGD:5509061 20191219 MGI PMID:24713655 1615099 Trp53inp2 transformation related protein 53 inducible nuclear protein 2 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20191219 MGI PMID:24713655 1615102 Rnf166 ring finger protein 166 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20231207 MGI 1615102 Rnf166 ring finger protein 166 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1615102 Rnf166 ring finger protein 166 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 1615102 Rnf166 ring finger protein 166 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20231207 MGI 1615105 Polr3g polymerase (RNA) III (DNA directed) polypeptide G gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20201001 MGI PMID:32576691 1615105 Polr3g polymerase (RNA) III (DNA directed) polypeptide G gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20201001 MGI PMID:32576691 1615105 Polr3g polymerase (RNA) III (DNA directed) polypeptide G gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615107 Mtfr1 mitochondrial fission regulator 1 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:17709566 1615107 Mtfr1 mitochondrial fission regulator 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20200310 MGI PMID:20568109 1615108 Mmd monocyte to macrophage differentiation-associated gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1615108 Mmd monocyte to macrophage differentiation-associated gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210520 MGI 1615108 Mmd monocyte to macrophage differentiation-associated gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1615108 Mmd monocyte to macrophage differentiation-associated gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20210520 MGI 1615108 Mmd monocyte to macrophage differentiation-associated gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20221215 MGI 1615108 Mmd monocyte to macrophage differentiation-associated gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20210520 MGI PMID:33421113 1615108 Mmd monocyte to macrophage differentiation-associated gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1615108 Mmd monocyte to macrophage differentiation-associated gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20210520 MGI PMID:33421113 1615108 Mmd monocyte to macrophage differentiation-associated gene MP:0009624 small inguinal lymph nodes IAGP N RGD:5509061 20210520 MGI PMID:33421113 1615108 Mmd monocyte to macrophage differentiation-associated gene MP:0010052 increased grip strength IEA N RGD:5509061 20210520 MGI 1615108 Mmd monocyte to macrophage differentiation-associated gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20210520 MGI PMID:33421113 1615108 Mmd monocyte to macrophage differentiation-associated gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210520 MGI 1615109 Ikbip IKBKB interacting protein gene MP:0001861 lung inflammation IAGP N RGD:5509061 20210610 MGI PMID:31826938 1615109 Ikbip IKBKB interacting protein gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20210610 MGI PMID:31826938 1615109 Ikbip IKBKB interacting protein gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20210610 MGI PMID:31826938 1615109 Ikbip IKBKB interacting protein gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20210610 MGI PMID:31826938 1615109 Ikbip IKBKB interacting protein gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20210610 MGI PMID:31826938 1615109 Ikbip IKBKB interacting protein gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20210610 MGI PMID:31826938 1615109 Ikbip IKBKB interacting protein gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20210610 MGI PMID:31826938 1615111 Ccdc127 coiled-coil domain containing 127 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1615111 Ccdc127 coiled-coil domain containing 127 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1615111 Ccdc127 coiled-coil domain containing 127 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1615112 Eps8l1 EPS8-like 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1615112 Eps8l1 EPS8-like 1 gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20210128 MGI 1615112 Eps8l1 EPS8-like 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1615114 Cylc1 cylicin, basic protein of sperm head cytoskeleton 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20240523 MGI PMID:38573307 1615114 Cylc1 cylicin, basic protein of sperm head cytoskeleton 1 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20240523 MGI PMID:38573307 1615114 Cylc1 cylicin, basic protein of sperm head cytoskeleton 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240523 MGI PMID:38573307 1615114 Cylc1 cylicin, basic protein of sperm head cytoskeleton 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240523 MGI PMID:38573307 1615114 Cylc1 cylicin, basic protein of sperm head cytoskeleton 1 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20240523 MGI PMID:38573307 1615114 Cylc1 cylicin, basic protein of sperm head cytoskeleton 1 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20240523 MGI PMID:38573307 1615115 Them5 thioesterase superfamily member 5 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22586271 1615115 Them5 thioesterase superfamily member 5 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:22586271 1615115 Them5 thioesterase superfamily member 5 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22586271 1615115 Them5 thioesterase superfamily member 5 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:22586271 1615115 Them5 thioesterase superfamily member 5 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:22586271 1615115 Them5 thioesterase superfamily member 5 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:22586271 1615115 Them5 thioesterase superfamily member 5 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:22586271 1615115 Them5 thioesterase superfamily member 5 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20141003 MGI PMID:22586271 1615117 Lage3 L antigen family, member 3 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1615117 Lage3 L antigen family, member 3 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20221215 MGI 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0014117 increased pancreatic beta cell apoptosis IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0020352 abnormal endoplasmic reticulum physiology IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615118 Ier3ip1 immediate early response 3 interacting protein 1 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20240425 MGI PMID:36322741 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170601 MGI PMID:26438849 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20170601 MGI PMID:26438849 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0001393 ataxia IAGP N RGD:5509061 20170601 MGI PMID:26438849 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20170105 MGI 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0002083 premature death IAGP N RGD:5509061 20170601 MGI PMID:26438849 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20170601 MGI PMID:26438849 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0002833 increased heart weight IEA N RGD:5509061 20220811 MGI 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20170601 MGI PMID:26438849 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20170601 MGI PMID:26438849 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20170601 MGI PMID:26438849 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220519 MGI 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0005405 axon degeneration IAGP N RGD:5509061 20170601 MGI PMID:26438849 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20220811 MGI 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20170601 MGI PMID:26438849 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20170601 MGI PMID:26438849 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0009978 abnormal cerebellum white matter morphology IAGP N RGD:5509061 20170601 MGI PMID:26438849 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20170105 MGI 1615120 Sptssb serine palmitoyltransferase, small subunit B gene MP:0020353 abnormal endoplasmic reticulum stress IAGP N RGD:5509061 20170601 MGI PMID:26438849 1615121 Nop10 NOP10 ribonucleoprotein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1615121 Nop10 NOP10 ribonucleoprotein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615121 Nop10 NOP10 ribonucleoprotein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1615123 Med11 mediator complex subunit 11 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20160421 MGI 1615123 Med11 mediator complex subunit 11 gene MP:0002861 abnormal tail bud morphology IEA N RGD:5509061 20160811 MGI 1615123 Med11 mediator complex subunit 11 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20221215 MGI 1615123 Med11 mediator complex subunit 11 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615123 Med11 mediator complex subunit 11 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 1615123 Med11 mediator complex subunit 11 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1615124 Niban3 niban apoptosis regulator 3 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210128 MGI 1615124 Niban3 niban apoptosis regulator 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210520 MGI 1615124 Niban3 niban apoptosis regulator 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210520 MGI 1615124 Niban3 niban apoptosis regulator 3 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20200220 MGI PMID:31412363 1615124 Niban3 niban apoptosis regulator 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1615124 Niban3 niban apoptosis regulator 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1615124 Niban3 niban apoptosis regulator 3 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20200220 MGI PMID:31412363 1615124 Niban3 niban apoptosis regulator 3 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20200220 MGI PMID:31412363 1615124 Niban3 niban apoptosis regulator 3 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200220 MGI PMID:31412363 1615124 Niban3 niban apoptosis regulator 3 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20200220 MGI PMID:31412363 1615124 Niban3 niban apoptosis regulator 3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200220 MGI PMID:31412363 1615124 Niban3 niban apoptosis regulator 3 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20200220 MGI PMID:31412363 1615124 Niban3 niban apoptosis regulator 3 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20200220 MGI PMID:31412363 1615124 Niban3 niban apoptosis regulator 3 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20200220 MGI PMID:31412363 1615124 Niban3 niban apoptosis regulator 3 gene MP:0008188 abnormal transitional stage B cell morphology IAGP N RGD:5509061 20200220 MGI PMID:31412363 1615124 Niban3 niban apoptosis regulator 3 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20200220 MGI PMID:31412363 1615124 Niban3 niban apoptosis regulator 3 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20200220 MGI PMID:31412363 1615124 Niban3 niban apoptosis regulator 3 gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20200220 MGI PMID:31412363 1615124 Niban3 niban apoptosis regulator 3 gene MP:0009925 increased transitional stage T2 B cell number IAGP N RGD:5509061 20200220 MGI PMID:31412363 1615124 Niban3 niban apoptosis regulator 3 gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:31412363 1615124 Niban3 niban apoptosis regulator 3 gene MP:0020155 enhanced humoral immune response IAGP N RGD:5509061 20200220 MGI PMID:31412363 1615126 S100a14 S100 calcium binding protein A14 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1615126 S100a14 S100 calcium binding protein A14 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1615126 S100a14 S100 calcium binding protein A14 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 1615126 S100a14 S100 calcium binding protein A14 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20160421 MGI 1615129 Uqcr10 ubiquinol-cytochrome c reductase, complex III subunit X gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20240926 MGI 1615129 Uqcr10 ubiquinol-cytochrome c reductase, complex III subunit X gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20240926 MGI 1615129 Uqcr10 ubiquinol-cytochrome c reductase, complex III subunit X gene MP:0002582 disorganized extraembryonic tissue IEA N RGD:5509061 20240926 MGI 1615129 Uqcr10 ubiquinol-cytochrome c reductase, complex III subunit X gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20240926 MGI 1615129 Uqcr10 ubiquinol-cytochrome c reductase, complex III subunit X gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20240926 MGI 1615129 Uqcr10 ubiquinol-cytochrome c reductase, complex III subunit X gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1615129 Uqcr10 ubiquinol-cytochrome c reductase, complex III subunit X gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200310 MGI 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:23530063 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200310 MGI PMID:23530063 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20200310 MGI PMID:23530063 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:23530063 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:23530063 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:23530063 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20200310 MGI 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:23530063 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20200310 MGI PMID:23530063 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0005440 increased glycogen level IAGP N RGD:5509061 20200310 MGI PMID:23530063 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20210128 MGI 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:23530063 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20200310 MGI PMID:23530063 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20200310 MGI PMID:23530063 1615130 Dnajc15 DnaJ heat shock protein family (Hsp40) member C15 gene MP:0031003 increased kidney glycogen level IAGP N RGD:5509061 20200310 MGI PMID:23530063 1615131 Necap2 NECAP endocytosis associated 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1615131 Necap2 NECAP endocytosis associated 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1615131 Necap2 NECAP endocytosis associated 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240627 MGI 1615131 Necap2 NECAP endocytosis associated 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 1615133 Chchd1 coiled-coil-helix-coiled-coil-helix domain containing 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200310 MGI 1615133 Chchd1 coiled-coil-helix-coiled-coil-helix domain containing 1 gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1615133 Chchd1 coiled-coil-helix-coiled-coil-helix domain containing 1 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20200310 MGI 1615133 Chchd1 coiled-coil-helix-coiled-coil-helix domain containing 1 gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1615133 Chchd1 coiled-coil-helix-coiled-coil-helix domain containing 1 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20200310 MGI 1615133 Chchd1 coiled-coil-helix-coiled-coil-helix domain containing 1 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20200310 MGI 1615133 Chchd1 coiled-coil-helix-coiled-coil-helix domain containing 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1615133 Chchd1 coiled-coil-helix-coiled-coil-helix domain containing 1 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20200310 MGI 1615133 Chchd1 coiled-coil-helix-coiled-coil-helix domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200310 MGI 1615134 Tomm6 translocase of outer mitochondrial membrane 6 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1615134 Tomm6 translocase of outer mitochondrial membrane 6 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1615134 Tomm6 translocase of outer mitochondrial membrane 6 gene MP:0000613 abnormal salivary gland morphology IEA N RGD:5509061 20210520 MGI 1615134 Tomm6 translocase of outer mitochondrial membrane 6 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1615134 Tomm6 translocase of outer mitochondrial membrane 6 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210826 MGI 1615134 Tomm6 translocase of outer mitochondrial membrane 6 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1615134 Tomm6 translocase of outer mitochondrial membrane 6 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1615134 Tomm6 translocase of outer mitochondrial membrane 6 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1615134 Tomm6 translocase of outer mitochondrial membrane 6 gene MP:0011971 increased circulating lactate dehydrogenase level IEA N RGD:5509061 20240523 MGI 1615135 Mtarc1 mitochondrial amidoxime reducing component 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20240509 MGI PMID:38437227 1615135 Mtarc1 mitochondrial amidoxime reducing component 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20230119 MGI 1615135 Mtarc1 mitochondrial amidoxime reducing component 1 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20240509 MGI PMID:38437227 1615135 Mtarc1 mitochondrial amidoxime reducing component 1 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20240509 MGI PMID:38437227 1615135 Mtarc1 mitochondrial amidoxime reducing component 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230119 MGI 1615135 Mtarc1 mitochondrial amidoxime reducing component 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230119 MGI 1615135 Mtarc1 mitochondrial amidoxime reducing component 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20230119 MGI 1615135 Mtarc1 mitochondrial amidoxime reducing component 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20240509 MGI PMID:38437227 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0000747 muscle weakness IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220519 MGI 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220519 MGI 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0005400 abnormal vitamin level IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0010052 increased grip strength IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220519 MGI 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0030642 decreased methionine level IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0030659 decreased glycine level IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0030691 increased serine level IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0030698 decreased phenylalanine level IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0030700 increased threonine level IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0030707 decreased glutamine level IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0030732 increased gamma-aminobutyric acid level IAGP N RGD:5509061 20191107 MGI PMID:30327125 1615139 Pdxp pyridoxal (pyridoxine, vitamin B6) phosphatase gene MP:0031640 increased alanine level IAGP N RGD:5509061 20240801 MGI PMID:30327125 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0001655 multifocal hepatic necrosis IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0001836 abnormal antigen presentation via MHC class I IAGP N RGD:5509061 20200310 MGI PMID:16415873 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20200310 MGI PMID:24778236 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:16415873 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:16415873 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20200310 MGI PMID:16415873 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20200310 MGI PMID:20457904 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20200310 MGI PMID:24778236 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0003326 liver failure IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0005041 abnormal antigen presentation via MHC class II IAGP N RGD:5509061 20200310 MGI PMID:16415873 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0005461 abnormal dendritic cell morphology IAGP N RGD:5509061 20200310 MGI PMID:20457904 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0005461 abnormal dendritic cell morphology IAGP N RGD:5509061 20200310 MGI PMID:24778236 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008548 abnormal circulating interferon level IAGP N RGD:5509061 20200310 MGI PMID:16415873 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20200310 MGI PMID:16415873 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008556 abnormal tumor necrosis factor secretion IAGP N RGD:5509061 20200310 MGI PMID:16415873 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008562 increased interferon-alpha secretion IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20200310 MGI PMID:24778236 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008648 decreased circulating interleukin-12b level IAGP N RGD:5509061 20200310 MGI PMID:24778236 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20200310 MGI PMID:16415873 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20200310 MGI PMID:20457904 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20200310 MGI PMID:20457904 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20200310 MGI PMID:24778236 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20200310 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210218 MGI PMID:21683627 1615140 Unc93b1 unc-93 homolog B1, TLR signaling regulator gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:16415873 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20211021 MGI 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11719692 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11934864 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:15753313 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11719692 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11934864 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17875220 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220519 MGI 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:11719692 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:11719692 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:11934864 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:15753313 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11719692 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11719692 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:11719692 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:11934864 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11934864 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20240627 MGI PMID:38627502 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17687327 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20240627 MGI PMID:38627502 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:11719692 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:11934864 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20240627 MGI PMID:38627502 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:17875220 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11719692 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:11719692 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:11719692 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:15753313 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20240627 MGI PMID:38627502 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20240627 MGI PMID:38627502 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:15753313 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20240627 MGI PMID:38627502 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0009203 external male genitalia hypoplasia IAGP N RGD:5509061 20240627 MGI PMID:38627502 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:11719692 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:11719692 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11719692 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11934864 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15753313 1615141 Dnmt3l DNA methyltransferase 3-like gene MP:0020515 abnormal visceral yolk sac endoderm morphology IAGP N RGD:5509061 20180125 MGI PMID:11719692 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0001661 extended life span IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0002083 premature death IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20180913 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0005635 decreased circulating bilirubin level IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0012230 abnormal sphingolipid level IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20180726 MGI PMID:28506826 1615142 Ndufa1 NADH:ubiquinone oxidoreductase subunit A1 gene MP:0030636 decreased taurine level IAGP N RGD:5509061 20180913 MGI PMID:28506826 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0000601 small liver IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0002223 lymphoid hypoplasia IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0003641 small lung IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0003717 pallor IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0006098 absent cerebellar lobules IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0010866 abnormal prenatal body size IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0011038 impaired branching involved in alveolar sac morphogenesis IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0011525 abnormal placenta intervillous maternal lacunae morphology IAGP N RGD:5509061 20160929 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0014399 decreased hematopoietic precursor cell number IAGP N RGD:5509061 20240321 MGI PMID:26774856 1615144 Fubp1 far upstream element (FUSE) binding protein 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1615146 Rif1 replication timing regulatory factor 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19948482 1615146 Rif1 replication timing regulatory factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19948482 1615146 Rif1 replication timing regulatory factor 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23333305 1615146 Rif1 replication timing regulatory factor 1 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:23333305 1615146 Rif1 replication timing regulatory factor 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:19948482 1615146 Rif1 replication timing regulatory factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22850673 1615146 Rif1 replication timing regulatory factor 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23333305 1615146 Rif1 replication timing regulatory factor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23333305 1615146 Rif1 replication timing regulatory factor 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:19948482 1615146 Rif1 replication timing regulatory factor 1 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:23333305 1615146 Rif1 replication timing regulatory factor 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:23333305 1615146 Rif1 replication timing regulatory factor 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:23333305 1615146 Rif1 replication timing regulatory factor 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:23333305 1615146 Rif1 replication timing regulatory factor 1 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:23333305 1615146 Rif1 replication timing regulatory factor 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:23333305 1615146 Rif1 replication timing regulatory factor 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:23333305 1615146 Rif1 replication timing regulatory factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19948482 1615146 Rif1 replication timing regulatory factor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19948482 1615146 Rif1 replication timing regulatory factor 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23333305 1615146 Rif1 replication timing regulatory factor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19948482 1615146 Rif1 replication timing regulatory factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23333305 1615146 Rif1 replication timing regulatory factor 1 gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20141003 MGI PMID:24025402 1615147 Spag6l sperm associated antigen 6-like gene MP:0000434 megacephaly IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0009234 absent sperm head IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20200310 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20220811 MGI PMID:12167721 1615147 Spag6l sperm associated antigen 6-like gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220811 MGI PMID:12167721 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:18400903 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12023301 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12023301 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10700185 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:10700185 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10700185 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10700185 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:10700185 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18691547 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16234809 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0003247 abnormal glutaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16234809 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:10700185 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22787056 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0005426 tachypnea IAGP N RGD:5509061 20141003 MGI PMID:10700185 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:18400903 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18691547 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:10700185 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10700185 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0021091 abnormal dorsal interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:12023301 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0021093 abnormal dorsal interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:12023301 1615148 Tlx3 T cell leukemia, homeobox 3 gene MP:0021095 abnormal dorsal interneuron 4 morphology IAGP N RGD:5509061 20220310 MGI PMID:12023301 1615149 Tnfsf9 tumor necrosis factor (ligand) superfamily, member 9 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:10528184 1615149 Tnfsf9 tumor necrosis factor (ligand) superfamily, member 9 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10528184 1615150 Tnfsf8 tumor necrosis factor (ligand) superfamily, member 8 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220811 MGI 1615150 Tnfsf8 tumor necrosis factor (ligand) superfamily, member 8 gene MP:0001148 enlarged testis IEA N RGD:5509061 20220811 MGI 1615150 Tnfsf8 tumor necrosis factor (ligand) superfamily, member 8 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1615150 Tnfsf8 tumor necrosis factor (ligand) superfamily, member 8 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1615150 Tnfsf8 tumor necrosis factor (ligand) superfamily, member 8 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1615150 Tnfsf8 tumor necrosis factor (ligand) superfamily, member 8 gene MP:0005673 decreased susceptibility to graft versus host disease IAGP N RGD:5509061 20141003 MGI PMID:15322151 1615151 Cd40lg CD40 ligand gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:17202317 1615151 Cd40lg CD40 ligand gene MP:0000414 alopecia IAGP N RGD:5509061 20200310 MGI PMID:9036998 1615151 Cd40lg CD40 ligand gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20200310 MGI PMID:7882172 1615151 Cd40lg CD40 ligand gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20200310 MGI PMID:15885854 1615151 Cd40lg CD40 ligand gene MP:0001212 skin lesions IAGP N RGD:5509061 20200310 MGI PMID:9036998 1615151 Cd40lg CD40 ligand gene MP:0001661 extended life span IAGP N RGD:5509061 20200310 MGI PMID:9036998 1615151 Cd40lg CD40 ligand gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20200310 MGI PMID:7882172 1615151 Cd40lg CD40 ligand gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20200310 MGI PMID:7964465 1615151 Cd40lg CD40 ligand gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20200310 MGI PMID:22761313 1615151 Cd40lg CD40 ligand gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20200310 MGI PMID:9036998 1615151 Cd40lg CD40 ligand gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20200310 MGI PMID:24030045 1615151 Cd40lg CD40 ligand gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20200310 MGI PMID:24030045 1615151 Cd40lg CD40 ligand gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20200310 MGI PMID:7882172 1615151 Cd40lg CD40 ligand gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20200310 MGI PMID:7964465 1615151 Cd40lg CD40 ligand gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20200310 MGI PMID:7964465 1615151 Cd40lg CD40 ligand gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:9036998 1615151 Cd40lg CD40 ligand gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:7882172 1615151 Cd40lg CD40 ligand gene MP:0002183 gliosis IAGP N RGD:5509061 20200310 MGI PMID:12402041 1615151 Cd40lg CD40 ligand gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200310 MGI PMID:15071493 1615151 Cd40lg CD40 ligand gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20200310 MGI PMID:7964465 1615151 Cd40lg CD40 ligand gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20200310 MGI PMID:7882172 1615151 Cd40lg CD40 ligand gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:7882172 1615151 Cd40lg CD40 ligand gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:7964465 1615151 Cd40lg CD40 ligand gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:9036998 1615151 Cd40lg CD40 ligand gene MP:0002491 decreased IgD level IAGP N RGD:5509061 20200310 MGI PMID:7882172 1615151 Cd40lg CD40 ligand gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20200310 MGI PMID:7882172 1615151 Cd40lg CD40 ligand gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20200310 MGI PMID:7964465 1615151 Cd40lg CD40 ligand gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20200310 MGI PMID:11875495 1615151 Cd40lg CD40 ligand gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20200310 MGI PMID:15071493 1615151 Cd40lg CD40 ligand gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20200310 MGI PMID:7964465 1615151 Cd40lg CD40 ligand gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200310 MGI PMID:24030045 1615151 Cd40lg CD40 ligand gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20200310 MGI PMID:15071493 1615151 Cd40lg CD40 ligand gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20200310 MGI PMID:12402041 1615151 Cd40lg CD40 ligand gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20200310 MGI PMID:15795333 1615151 Cd40lg CD40 ligand gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20200310 MGI PMID:15071493 1615151 Cd40lg CD40 ligand gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20200310 MGI PMID:9036998 1615151 Cd40lg CD40 ligand gene MP:0004031 insulitis IAGP N RGD:5509061 20200310 MGI PMID:15467837 1615151 Cd40lg CD40 ligand gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20200310 MGI PMID:9036998 1615151 Cd40lg CD40 ligand gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20200310 MGI PMID:15467837 1615151 Cd40lg CD40 ligand gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20200310 MGI PMID:15467837 1615151 Cd40lg CD40 ligand gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20200310 MGI PMID:22761313 1615151 Cd40lg CD40 ligand gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20200310 MGI PMID:7882172 1615151 Cd40lg CD40 ligand gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20200310 MGI PMID:7964465 1615151 Cd40lg CD40 ligand gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20200310 MGI PMID:15467837 1615151 Cd40lg CD40 ligand gene MP:0005002 abnormal T cell clonal deletion IAGP N RGD:5509061 20200310 MGI PMID:11342622 1615151 Cd40lg CD40 ligand gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20200310 MGI PMID:12871426 1615151 Cd40lg CD40 ligand gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:7882172 1615151 Cd40lg CD40 ligand gene MP:0005364 increased susceptibility to prion infection IAGP N RGD:5509061 20200310 MGI PMID:15071493 1615151 Cd40lg CD40 ligand gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20200310 MGI PMID:7882172 1615151 Cd40lg CD40 ligand gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20200310 MGI PMID:12871426 1615151 Cd40lg CD40 ligand gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:11230105 1615151 Cd40lg CD40 ligand gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20200310 MGI PMID:15795333 1615151 Cd40lg CD40 ligand gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:7882172 1615151 Cd40lg CD40 ligand gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:7964465 1615151 Cd40lg CD40 ligand gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20200310 MGI PMID:17360404 1615151 Cd40lg CD40 ligand gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20200310 MGI PMID:7882172 1615151 Cd40lg CD40 ligand gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20200310 MGI PMID:7964465 1615151 Cd40lg CD40 ligand gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:24030045 1615151 Cd40lg CD40 ligand gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:7882172 1615151 Cd40lg CD40 ligand gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:7964465 1615151 Cd40lg CD40 ligand gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:24030045 1615151 Cd40lg CD40 ligand gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20200310 MGI PMID:7964465 1615151 Cd40lg CD40 ligand gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20200310 MGI PMID:24030045 1615151 Cd40lg CD40 ligand gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20200310 MGI PMID:7882172 1615151 Cd40lg CD40 ligand gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:24030045 1615151 Cd40lg CD40 ligand gene MP:0008523 absent lymph node germinal center IAGP N RGD:5509061 20200310 MGI PMID:7964465 1615151 Cd40lg CD40 ligand gene MP:0008918 microgliosis IAGP N RGD:5509061 20200310 MGI PMID:15071493 1615151 Cd40lg CD40 ligand gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20200310 MGI PMID:12871426 1615151 Cd40lg CD40 ligand gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20200310 MGI PMID:15795333 1615151 Cd40lg CD40 ligand gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20200310 MGI PMID:17202317 1615151 Cd40lg CD40 ligand gene MP:0010962 decreased compact bone mass IAGP N RGD:5509061 20200310 MGI PMID:17202317 1615152 Cd40 CD40 antigen gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200310 MGI PMID:17202317 1615152 Cd40 CD40 antigen gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:7534202 1615152 Cd40 CD40 antigen gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:15485634 1615152 Cd40 CD40 antigen gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:15485634 1615152 Cd40 CD40 antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20200310 MGI PMID:7534202 1615152 Cd40 CD40 antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20200310 MGI PMID:9088978 1615152 Cd40 CD40 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20200310 MGI PMID:11418692 1615152 Cd40 CD40 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20200310 MGI PMID:11418692 1615152 Cd40 CD40 antigen gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20200310 MGI PMID:9088978 1615152 Cd40 CD40 antigen gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20200310 MGI PMID:7534202 1615152 Cd40 CD40 antigen gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20200310 MGI PMID:9088978 1615152 Cd40 CD40 antigen gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15128830 1615152 Cd40 CD40 antigen gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20200310 MGI PMID:21441458 1615152 Cd40 CD40 antigen gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20200310 MGI PMID:14670300 1615152 Cd40 CD40 antigen gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:14670300 1615152 Cd40 CD40 antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20200310 MGI PMID:18624351 1615152 Cd40 CD40 antigen gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:7534202 1615152 Cd40 CD40 antigen gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:11418692 1615152 Cd40 CD40 antigen gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20200310 MGI PMID:11418692 1615152 Cd40 CD40 antigen gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20200310 MGI PMID:7534202 1615152 Cd40 CD40 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:11418692 1615152 Cd40 CD40 antigen gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20200310 MGI PMID:16973390 1615152 Cd40 CD40 antigen gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20200310 MGI PMID:16973390 1615152 Cd40 CD40 antigen gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20200310 MGI PMID:16973390 1615152 Cd40 CD40 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20200310 MGI PMID:16973390 1615152 Cd40 CD40 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:23027924 1615152 Cd40 CD40 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:9088978 1615152 Cd40 CD40 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:9088978 1615152 Cd40 CD40 antigen gene MP:0005612 decreased susceptibility to type II hypersensitivity reaction IAGP N RGD:5509061 20200310 MGI PMID:10760808 1615152 Cd40 CD40 antigen gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20200310 MGI PMID:11418692 1615152 Cd40 CD40 antigen gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20200310 MGI PMID:15795333 1615152 Cd40 CD40 antigen gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20200310 MGI PMID:18624351 1615152 Cd40 CD40 antigen gene MP:0008179 absent germinal center B cells IAGP N RGD:5509061 20200310 MGI PMID:23027924 1615152 Cd40 CD40 antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20200310 MGI PMID:16973390 1615152 Cd40 CD40 antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20200310 MGI PMID:18624351 1615152 Cd40 CD40 antigen gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20200310 MGI PMID:18624351 1615152 Cd40 CD40 antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20200310 MGI PMID:9088978 1615152 Cd40 CD40 antigen gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20200310 MGI PMID:16973390 1615152 Cd40 CD40 antigen gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20200310 MGI PMID:11418692 1615152 Cd40 CD40 antigen gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20200310 MGI PMID:16973390 1615152 Cd40 CD40 antigen gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20200310 MGI PMID:7534202 1615152 Cd40 CD40 antigen gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20200310 MGI PMID:9088978 1615152 Cd40 CD40 antigen gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20200310 MGI PMID:9088978 1615152 Cd40 CD40 antigen gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20200310 MGI PMID:9088978 1615152 Cd40 CD40 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:11418692 1615152 Cd40 CD40 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:7534202 1615152 Cd40 CD40 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:9088978 1615152 Cd40 CD40 antigen gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:7534202 1615152 Cd40 CD40 antigen gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:9088978 1615152 Cd40 CD40 antigen gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20200310 MGI PMID:11418692 1615152 Cd40 CD40 antigen gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20200310 MGI PMID:7534202 1615152 Cd40 CD40 antigen gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20200310 MGI PMID:9088978 1615152 Cd40 CD40 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20200310 MGI PMID:7534202 1615152 Cd40 CD40 antigen gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20200310 MGI PMID:9088978 1615152 Cd40 CD40 antigen gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20200310 MGI PMID:11418692 1615152 Cd40 CD40 antigen gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20200310 MGI PMID:9088978 1615152 Cd40 CD40 antigen gene MP:0008523 absent lymph node germinal center IAGP N RGD:5509061 20200310 MGI PMID:9088978 1615152 Cd40 CD40 antigen gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:21441458 1615152 Cd40 CD40 antigen gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20200310 MGI PMID:15795333 1615152 Cd40 CD40 antigen gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20200310 MGI PMID:30013024 1615152 Cd40 CD40 antigen gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20200310 MGI PMID:17202317 1615152 Cd40 CD40 antigen gene MP:0010962 decreased compact bone mass IAGP N RGD:5509061 20200310 MGI PMID:17202317 1615152 Cd40 CD40 antigen gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20200310 MGI 1615152 Cd40 CD40 antigen gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20200310 MGI PMID:16973390 1615153 Tnfrsf18 tumor necrosis factor receptor superfamily, member 18 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:12070049 1615153 Tnfrsf18 tumor necrosis factor receptor superfamily, member 18 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1615153 Tnfrsf18 tumor necrosis factor receptor superfamily, member 18 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:12070049 1615153 Tnfrsf18 tumor necrosis factor receptor superfamily, member 18 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12070049 1615153 Tnfrsf18 tumor necrosis factor receptor superfamily, member 18 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12070049 1615153 Tnfrsf18 tumor necrosis factor receptor superfamily, member 18 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:12070049 1615154 Tnfaip6 tumor necrosis factor alpha induced protein 6 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:12668637 1615154 Tnfaip6 tumor necrosis factor alpha induced protein 6 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23118230 1615154 Tnfaip6 tumor necrosis factor alpha induced protein 6 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12668637 1615154 Tnfaip6 tumor necrosis factor alpha induced protein 6 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:23118230 1615154 Tnfaip6 tumor necrosis factor alpha induced protein 6 gene MP:0009374 absent cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:12668637 1615154 Tnfaip6 tumor necrosis factor alpha induced protein 6 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:12668637 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:11009421 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21341261 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23602765 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160721 MGI PMID:24878851 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:11009421 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:11009421 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11009421 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15334086 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0001577 anemia IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15334086 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11009421 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:11009421 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:11009421 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11009421 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11009421 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15334086 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0002083 premature death IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21341261 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:21341261 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:11009421 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15334086 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:21341261 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11009421 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23602765 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:15334086 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005150 cachexia IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21341261 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:11009421 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23602765 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23602765 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008164 abnormal B-1a B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008170 decreased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:21341261 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:23602765 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:23602765 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:23602765 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20705491 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0008976 delayed female fertility IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0009018 short estrus IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0009080 uterus inflammation IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0009246 pale spleen IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:21341261 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0009505 abnormal mammary gland lobule morphology IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11009421 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20151224 MGI PMID:24498102 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23602765 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11009421 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0012075 impaired mammary gland growth during pregnancy IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0013415 increased myeloid cell number in bone marrow IAGP N RGD:5509061 20160721 MGI PMID:24878851 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20160721 MGI PMID:24878851 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0013772 increased effector memory T-helper cell number IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:20530205 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0021029 increased tumor necrosis factor (ligand) superfamily member 11 level IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0021032 increased tumor necrosis factor receptor superfamily member 11b level IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615155 Tnfaip3 tumor necrosis factor, alpha-induced protein 3 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220616 MGI PMID:35464428 1615156 Tnc tenascin C gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16553788 1615156 Tnc tenascin C gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:8660327 1615156 Tnc tenascin C gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12177213 1615156 Tnc tenascin C gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:8660327 1615156 Tnc tenascin C gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:12177213 1615156 Tnc tenascin C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:1383086 1615156 Tnc tenascin C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8692862 1615156 Tnc tenascin C gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:8660327 1615156 Tnc tenascin C gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:16553788 1615156 Tnc tenascin C gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:16553788 1615156 Tnc tenascin C gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:8660327 1615156 Tnc tenascin C gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:8660327 1615156 Tnc tenascin C gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16553788 1615156 Tnc tenascin C gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:8660327 1615156 Tnc tenascin C gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:16553788 1615156 Tnc tenascin C gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:8660327 1615157 Tspan7 tetraspanin 7 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1615157 Tspan7 tetraspanin 7 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20220519 MGI 1615157 Tspan7 tetraspanin 7 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20200310 MGI PMID:28968657 1615157 Tspan7 tetraspanin 7 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220519 MGI 1615157 Tspan7 tetraspanin 7 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20200310 MGI PMID:28968657 1615157 Tspan7 tetraspanin 7 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:28968657 1615157 Tspan7 tetraspanin 7 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200310 MGI PMID:28968657 1615157 Tspan7 tetraspanin 7 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20200310 MGI PMID:28968657 1615157 Tspan7 tetraspanin 7 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20200310 MGI PMID:28968657 1615157 Tspan7 tetraspanin 7 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:28968657 1615157 Tspan7 tetraspanin 7 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200310 MGI PMID:28968657 1615157 Tspan7 tetraspanin 7 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20200310 MGI PMID:28968657 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:17953618 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:9394001 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:18235445 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:9394001 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20141003 MGI PMID:12571103 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20141003 MGI PMID:9394001 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:17953618 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:12571103 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:10706625 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10706625 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:17953618 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001357 increased aggression towards humans IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17953618 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:9394001 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:18235445 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17953618 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:10706625 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0002061 abnormal aggression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:9394001 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:22290436 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:9394001 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9394001 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22290436 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10706625 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10706625 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10706625 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0004166 abnormal limbic system morphology IAGP N RGD:5509061 20141003 MGI PMID:9394001 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0004171 abnormal pallium development IAGP N RGD:5509061 20141003 MGI PMID:12571103 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:10706625 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:12571103 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:22290436 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10706625 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0005267 abnormal olfactory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9394001 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10706625 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22290436 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0005655 increased aggression IAGP N RGD:5509061 20141003 MGI PMID:9394001 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20141003 MGI PMID:10706625 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0006300 abnormal entorhinal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9394001 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22290436 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:9394001 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:17953618 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008431 abnormal short-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:18235445 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20141003 MGI PMID:9394001 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:9394001 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008509 disorganized retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:10706625 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:22290436 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:10706625 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:22290436 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:10706625 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:22290436 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20161117 MGI PMID:10706625 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:12571103 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18235445 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:11997145 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0020388 decreased radial glial cell number IAGP N RGD:5509061 20161117 MGI PMID:12571103 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0020537 decreased subiculum size IAGP N RGD:5509061 20180301 MGI PMID:9394001 1615158 Nr2e1 nuclear receptor subfamily 2, group E, member 1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:10706625 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:16652367 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:16179923 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16179923 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21732189 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0002898 absent cartilage IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16179923 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18543318 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615159 Sox5 SRY (sex determining region Y)-box 5 gene MP:0012514 pectus excavatum IAGP N RGD:5509061 20141003 MGI PMID:11702786 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:24234655 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:24234655 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:18794345 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:18794345 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:18794345 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:20079728 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24234655 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:15882093 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:9512512 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15882093 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:9512512 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:15882093 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:9512512 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:18794345 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0001357 increased aggression towards humans IAGP N RGD:5509061 20141003 MGI PMID:18794345 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20220421 MGI PMID:18794345 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:24234655 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:24234655 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15882093 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:9512512 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0002068 abnormal parental behavior IAGP N RGD:5509061 20141003 MGI PMID:15882093 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0002068 abnormal parental behavior IAGP N RGD:5509061 20141003 MGI PMID:9512512 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15882093 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24234655 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9512512 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:24234655 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:24234655 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20079728 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:15882093 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:9512512 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:18794345 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:18794345 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0003199 calcified muscle IAGP N RGD:5509061 20141003 MGI PMID:24234655 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18794345 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:20079728 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:15882093 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0004080 abnormal nucleus accumbens morphology IAGP N RGD:5509061 20141003 MGI PMID:15882093 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0004103 abnormal ventral striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:15882093 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:24234655 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:18794345 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0005267 abnormal olfactory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15882093 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:15882093 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:9512512 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:15882093 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:18794345 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:18794345 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:24234655 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:24234655 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:24234655 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:18794345 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24234655 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180531 MGI PMID:28337978 1615160 Sox1 SRY (sex determining region Y)-box 1 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20180531 MGI PMID:28337978 1615161 Sorl1 sortilin-related receptor, LDLR class A repeats-containing gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20181227 MGI 1615161 Sorl1 sortilin-related receptor, LDLR class A repeats-containing gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22986780 1615161 Sorl1 sortilin-related receptor, LDLR class A repeats-containing gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1615161 Sorl1 sortilin-related receptor, LDLR class A repeats-containing gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 1615161 Sorl1 sortilin-related receptor, LDLR class A repeats-containing gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:22986780 1615161 Sorl1 sortilin-related receptor, LDLR class A repeats-containing gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20200402 MGI 1615161 Sorl1 sortilin-related receptor, LDLR class A repeats-containing gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:22986780 1615161 Sorl1 sortilin-related receptor, LDLR class A repeats-containing gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:16174740 1615161 Sorl1 sortilin-related receptor, LDLR class A repeats-containing gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:19036982 1615161 Sorl1 sortilin-related receptor, LDLR class A repeats-containing gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:22986780 1615161 Sorl1 sortilin-related receptor, LDLR class A repeats-containing gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20141003 MGI PMID:22986780 1615161 Sorl1 sortilin-related receptor, LDLR class A repeats-containing gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:18618022 1615161 Sorl1 sortilin-related receptor, LDLR class A repeats-containing gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:18618022 1615161 Sorl1 sortilin-related receptor, LDLR class A repeats-containing gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20141003 MGI PMID:22986780 1615164 Snapin SNAP-associated protein gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20141003 MGI PMID:16280592 1615164 Snapin SNAP-associated protein gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1615164 Snapin SNAP-associated protein gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141016 MGI PMID:24373968 1615164 Snapin SNAP-associated protein gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141016 MGI PMID:24373968 1615164 Snapin SNAP-associated protein gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20201022 MGI 1615164 Snapin SNAP-associated protein gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1615164 Snapin SNAP-associated protein gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16280592 1615164 Snapin SNAP-associated protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615164 Snapin SNAP-associated protein gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1615175 Nfkbie nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, epsilon gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14665694 1615175 Nfkbie nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, epsilon gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14665694 1615175 Nfkbie nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, epsilon gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10570287 1615175 Nfkbie nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, epsilon gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10570287 1615175 Nfkbie nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, epsilon gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14665694 1615175 Nfkbie nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, epsilon gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:14665694 1615175 Nfkbie nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, epsilon gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:14665694 1615175 Nfkbie nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, epsilon gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:10570287 1615175 Nfkbie nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, epsilon gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14665694 1615175 Nfkbie nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, epsilon gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14665694 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12750314 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12750314 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:12750314 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:11439183 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12750314 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9846484 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:9768749 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17579027 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9846484 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:11254352 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:11254352 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12787506 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12787506 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16554754 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12750314 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12750314 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11439183 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12370307 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12787506 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9768749 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9846484 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001788 periorbital edema IAGP N RGD:5509061 20141003 MGI PMID:9768749 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17579027 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9846484 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:9846484 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17579027 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17579027 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17579027 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:9846484 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17579027 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:16554754 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20141003 MGI PMID:16554754 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11439183 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16554754 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12750314 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12750314 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:12750314 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:16554754 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:12370307 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12750314 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:12750314 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9846484 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9846484 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9846484 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17579027 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:9768749 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9768749 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:9846484 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12750314 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12750314 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0006261 annular pancreas IAGP N RGD:5509061 20141003 MGI PMID:16554754 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17579027 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17579027 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17579027 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17579027 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20240509 MGI PMID:38457343 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17579027 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16554754 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:11254352 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0009424 decreased extensor digitorum longus weight IAGP N RGD:5509061 20141003 MGI PMID:11254352 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0009426 decreased soleus weight IAGP N RGD:5509061 20141003 MGI PMID:11254352 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:12787506 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16554754 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:12750314 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12750314 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17579027 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9768749 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11439183 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11439183 1615176 Nfatc3 nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 3 gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:12750314 1615177 Rpsa ribosomal protein SA gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20200310 MGI PMID:14730304 1615177 Rpsa ribosomal protein SA gene MP:0003935 abnormal craniofacial development IEA N RGD:5509061 20200310 MGI 1615177 Rpsa ribosomal protein SA gene MP:0004201 fetal growth retardation IEA N RGD:5509061 20200310 MGI 1615177 Rpsa ribosomal protein SA gene MP:0005217 abnormal pancreatic beta cell morphology IEA N RGD:5509061 20200310 MGI 1615177 Rpsa ribosomal protein SA gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20200310 MGI 1615177 Rpsa ribosomal protein SA gene MP:0005648 heart right ventricle degeneration IAGP N RGD:5509061 20200310 MGI PMID:14730304 1615177 Rpsa ribosomal protein SA gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20200310 MGI 1615178 Lama3 laminin, alpha 3 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20190228 MGI PMID:27729280 1615178 Lama3 laminin, alpha 3 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20190228 MGI PMID:27729280 1615178 Lama3 laminin, alpha 3 gene MP:0001200 thick skin IAGP N RGD:5509061 20190228 MGI PMID:27729280 1615178 Lama3 laminin, alpha 3 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:10366601 1615178 Lama3 laminin, alpha 3 gene MP:0001208 blistering IAGP N RGD:5509061 20190228 MGI PMID:27729280 1615178 Lama3 laminin, alpha 3 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10366601 1615178 Lama3 laminin, alpha 3 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:10366601 1615178 Lama3 laminin, alpha 3 gene MP:0001235 disorganized suprabasal layer IAGP N RGD:5509061 20141003 MGI PMID:10366601 1615178 Lama3 laminin, alpha 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10366601 1615178 Lama3 laminin, alpha 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190228 MGI PMID:27729280 1615178 Lama3 laminin, alpha 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20170504 MGI PMID:21878500 1615178 Lama3 laminin, alpha 3 gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:10366601 1615178 Lama3 laminin, alpha 3 gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:10366601 1615178 Lama3 laminin, alpha 3 gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:10366601 1615178 Lama3 laminin, alpha 3 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20190228 MGI PMID:27729280 1615178 Lama3 laminin, alpha 3 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20170504 MGI PMID:21878500 1615178 Lama3 laminin, alpha 3 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20170504 MGI PMID:21878500 1615178 Lama3 laminin, alpha 3 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20170504 MGI PMID:21878500 1615178 Lama3 laminin, alpha 3 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20170504 MGI PMID:21878500 1615178 Lama3 laminin, alpha 3 gene MP:0008854 bleb IAGP N RGD:5509061 20190228 MGI PMID:27729280 1615178 Lama3 laminin, alpha 3 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20190228 MGI PMID:27729280 1615178 Lama3 laminin, alpha 3 gene MP:0010936 decreased airway resistance IAGP N RGD:5509061 20170504 MGI PMID:21878500 1615178 Lama3 laminin, alpha 3 gene MP:0010950 abnormal lung hysteresivity IAGP N RGD:5509061 20170504 MGI PMID:21878500 1615178 Lama3 laminin, alpha 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10366601 1615178 Lama3 laminin, alpha 3 gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20190228 MGI PMID:27729280 1615178 Lama3 laminin, alpha 3 gene MP:0014226 abnormal alveolar macrophage physiology IAGP N RGD:5509061 20170504 MGI PMID:21878500 1615178 Lama3 laminin, alpha 3 gene MP:0014228 increased alveolar macrophage number IAGP N RGD:5509061 20170504 MGI PMID:21878500 1615178 Lama3 laminin, alpha 3 gene MP:0020253 increased collagen level IAGP N RGD:5509061 20170504 MGI PMID:21878500 1615178 Lama3 laminin, alpha 3 gene MP:0020253 increased collagen level IAGP N RGD:5509061 20190228 MGI PMID:27729280 1615178 Lama3 laminin, alpha 3 gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20170504 MGI PMID:21878500 1615181 Krtap8-1 keratin associated protein 8-1 gene MP:0000162 lordosis IEA N RGD:5509061 20210826 MGI 1615181 Krtap8-1 keratin associated protein 8-1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1615181 Krtap8-1 keratin associated protein 8-1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1615181 Krtap8-1 keratin associated protein 8-1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210128 MGI 1615181 Krtap8-1 keratin associated protein 8-1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20211021 MGI 1615181 Krtap8-1 keratin associated protein 8-1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1615181 Krtap8-1 keratin associated protein 8-1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1615181 Krtap8-1 keratin associated protein 8-1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20211021 MGI 1615181 Krtap8-1 keratin associated protein 8-1 gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20240523 MGI 1615181 Krtap8-1 keratin associated protein 8-1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20210826 MGI 1615181 Krtap8-1 keratin associated protein 8-1 gene MP:0009709 hydrometra IEA N RGD:5509061 20210128 MGI 1615181 Krtap8-1 keratin associated protein 8-1 gene MP:0013764 decreased T-helper cell number IEA N RGD:5509061 20221215 MGI 1615185 Hsd3b6 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 6 gene MP:0001337 dry eyes IAGP N RGD:5509061 20240502 MGI PMID:37117756 1615185 Hsd3b6 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 6 gene MP:0001345 Meibomian gland atrophy IAGP N RGD:5509061 20240502 MGI PMID:37117756 1615185 Hsd3b6 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 6 gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20240502 MGI PMID:37117756 1615185 Hsd3b6 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 6 gene MP:0013388 small Meibomian gland IAGP N RGD:5509061 20240502 MGI PMID:37117756 1615185 Hsd3b6 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 6 gene MP:0013391 abnormal Meibomian gland physiology IAGP N RGD:5509061 20240502 MGI PMID:37117756 1615185 Hsd3b6 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 6 gene MP:0020219 increased tear production IAGP N RGD:5509061 20240502 MGI PMID:37117756 1615189 Hs3st3a1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3A1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230601 MGI 1615189 Hs3st3a1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3A1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1615189 Hs3st3a1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3A1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1615189 Hs3st3a1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3A1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1615189 Hs3st3a1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3A1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1615189 Hs3st3a1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3A1 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20231207 MGI 1615189 Hs3st3a1 heparan sulfate (glucosamine) 3-O-sulfotransferase 3A1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1615190 Hoxd9 homeobox D9 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615190 Hoxd9 homeobox D9 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:8625797 1615190 Hoxd9 homeobox D9 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:9892669 1615190 Hoxd9 homeobox D9 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615190 Hoxd9 homeobox D9 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:9892669 1615190 Hoxd9 homeobox D9 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:8625797 1615190 Hoxd9 homeobox D9 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:8625797 1615190 Hoxd9 homeobox D9 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8625797 1615190 Hoxd9 homeobox D9 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615190 Hoxd9 homeobox D9 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615190 Hoxd9 homeobox D9 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615190 Hoxd9 homeobox D9 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615190 Hoxd9 homeobox D9 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:8625797 1615190 Hoxd9 homeobox D9 gene MP:0003344 mammary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9892669 1615190 Hoxd9 homeobox D9 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615190 Hoxd9 homeobox D9 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:8625797 1615190 Hoxd9 homeobox D9 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20141003 MGI PMID:8625797 1615190 Hoxd9 homeobox D9 gene MP:0004614 caudal vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:8625797 1615190 Hoxd9 homeobox D9 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615190 Hoxd9 homeobox D9 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:8625797 1615190 Hoxd9 homeobox D9 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:8625797 1615190 Hoxd9 homeobox D9 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615190 Hoxd9 homeobox D9 gene MP:0004622 sacral vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0004622 sacral vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:8625797 1615190 Hoxd9 homeobox D9 gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615190 Hoxd9 homeobox D9 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:8625797 1615190 Hoxd9 homeobox D9 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:8625797 1615190 Hoxd9 homeobox D9 gene MP:0005353 abnormal patella morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615190 Hoxd9 homeobox D9 gene MP:0009005 abnormal sesamoid bone of gastrocnemius morphology IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:10642795 1615190 Hoxd9 homeobox D9 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615191 Hoxd8 homeobox D8 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11311170 1615191 Hoxd8 homeobox D8 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:11311170 1615191 Hoxd8 homeobox D8 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11311170 1615191 Hoxd8 homeobox D8 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11311170 1615191 Hoxd8 homeobox D8 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11311170 1615191 Hoxd8 homeobox D8 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11311170 1615191 Hoxd8 homeobox D8 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:11311170 1615191 Hoxd8 homeobox D8 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:11311170 1615192 Hoxd4 homeobox D4 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10559481 1615192 Hoxd4 homeobox D4 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7750651 1615192 Hoxd4 homeobox D4 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:7628700 1615192 Hoxd4 homeobox D4 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:7750651 1615192 Hoxd4 homeobox D4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10559481 1615192 Hoxd4 homeobox D4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10559481 1615192 Hoxd4 homeobox D4 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10559481 1615192 Hoxd4 homeobox D4 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7628700 1615192 Hoxd4 homeobox D4 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7750651 1615192 Hoxd4 homeobox D4 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:7750651 1615192 Hoxd4 homeobox D4 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:7750651 1615192 Hoxd4 homeobox D4 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20141003 MGI PMID:7628700 1615192 Hoxd4 homeobox D4 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7628700 1615192 Hoxd4 homeobox D4 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7750651 1615192 Hoxd4 homeobox D4 gene MP:0004659 abnormal odontoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:7750651 1615192 Hoxd4 homeobox D4 gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20141003 MGI PMID:10559481 1615192 Hoxd4 homeobox D4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7628700 1615193 Hoxd11 homeobox D11 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0000464 increased presacral vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:7816839 1615193 Hoxd11 homeobox D11 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0000524 decreased renal tubule number IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:11493536 1615193 Hoxd11 homeobox D11 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:12050119 1615193 Hoxd11 homeobox D11 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:7816839 1615193 Hoxd11 homeobox D11 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:9250683 1615193 Hoxd11 homeobox D11 gene MP:0000553 absent radius IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11688568 1615193 Hoxd11 homeobox D11 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7816839 1615193 Hoxd11 homeobox D11 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9250683 1615193 Hoxd11 homeobox D11 gene MP:0000555 absent carpal bone IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12217321 1615193 Hoxd11 homeobox D11 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12050119 1615193 Hoxd11 homeobox D11 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12217321 1615193 Hoxd11 homeobox D11 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18942146 1615193 Hoxd11 homeobox D11 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:7816839 1615193 Hoxd11 homeobox D11 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11688568 1615193 Hoxd11 homeobox D11 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12050119 1615193 Hoxd11 homeobox D11 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12217321 1615193 Hoxd11 homeobox D11 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18942146 1615193 Hoxd11 homeobox D11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11688568 1615193 Hoxd11 homeobox D11 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9250683 1615193 Hoxd11 homeobox D11 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11493536 1615193 Hoxd11 homeobox D11 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11688568 1615193 Hoxd11 homeobox D11 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12050119 1615193 Hoxd11 homeobox D11 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11688568 1615193 Hoxd11 homeobox D11 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:11688568 1615193 Hoxd11 homeobox D11 gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9250683 1615193 Hoxd11 homeobox D11 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1615193 Hoxd11 homeobox D11 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7816839 1615193 Hoxd11 homeobox D11 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9250683 1615193 Hoxd11 homeobox D11 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12050119 1615193 Hoxd11 homeobox D11 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0003600 ectopic kidney IAGP N RGD:5509061 20141003 MGI PMID:12050119 1615193 Hoxd11 homeobox D11 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:12050119 1615193 Hoxd11 homeobox D11 gene MP:0003613 abnormal kidney medulla development IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0003626 kidney medulla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11688568 1615193 Hoxd11 homeobox D11 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:11493536 1615193 Hoxd11 homeobox D11 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:12050119 1615193 Hoxd11 homeobox D11 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:11688568 1615193 Hoxd11 homeobox D11 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:11688568 1615193 Hoxd11 homeobox D11 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1615193 Hoxd11 homeobox D11 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1615193 Hoxd11 homeobox D11 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:11688568 1615193 Hoxd11 homeobox D11 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:12217321 1615193 Hoxd11 homeobox D11 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:11688568 1615193 Hoxd11 homeobox D11 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:12217321 1615193 Hoxd11 homeobox D11 gene MP:0004360 absent ulna IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1615193 Hoxd11 homeobox D11 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12869760 1615193 Hoxd11 homeobox D11 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615193 Hoxd11 homeobox D11 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7816839 1615193 Hoxd11 homeobox D11 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9250683 1615193 Hoxd11 homeobox D11 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:7816839 1615193 Hoxd11 homeobox D11 gene MP:0004638 elongated metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:12217321 1615193 Hoxd11 homeobox D11 gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:12217321 1615193 Hoxd11 homeobox D11 gene MP:0004649 decreased sacral vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0004650 increased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:12217321 1615193 Hoxd11 homeobox D11 gene MP:0004650 increased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0004650 increased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:7816839 1615193 Hoxd11 homeobox D11 gene MP:0004650 increased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:9250683 1615193 Hoxd11 homeobox D11 gene MP:0004656 absent sacral vertebrae IAGP N RGD:5509061 20141003 MGI PMID:12869760 1615193 Hoxd11 homeobox D11 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:11493536 1615193 Hoxd11 homeobox D11 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:7816839 1615193 Hoxd11 homeobox D11 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:9250683 1615193 Hoxd11 homeobox D11 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:12217321 1615193 Hoxd11 homeobox D11 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:7816839 1615193 Hoxd11 homeobox D11 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:9250683 1615193 Hoxd11 homeobox D11 gene MP:0005354 abnormal ilium morphology IAGP N RGD:5509061 20141003 MGI PMID:7816839 1615193 Hoxd11 homeobox D11 gene MP:0008159 increased diameter of fibula IAGP N RGD:5509061 20141003 MGI PMID:11493536 1615193 Hoxd11 homeobox D11 gene MP:0008161 increased diameter of radius IAGP N RGD:5509061 20141003 MGI PMID:12217321 1615193 Hoxd11 homeobox D11 gene MP:0008163 increased diameter of ulna IAGP N RGD:5509061 20141003 MGI PMID:12217321 1615193 Hoxd11 homeobox D11 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:11688568 1615193 Hoxd11 homeobox D11 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:12217321 1615193 Hoxd11 homeobox D11 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:7816839 1615193 Hoxd11 homeobox D11 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:9250683 1615193 Hoxd11 homeobox D11 gene MP:0009728 abnormal calcaneum morphology IAGP N RGD:5509061 20141003 MGI PMID:11688568 1615193 Hoxd11 homeobox D11 gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:12050119 1615193 Hoxd11 homeobox D11 gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:12050119 1615193 Hoxd11 homeobox D11 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:11493536 1615193 Hoxd11 homeobox D11 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11688568 1615193 Hoxd11 homeobox D11 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11688568 1615193 Hoxd11 homeobox D11 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0011366 absent metanephros IAGP N RGD:5509061 20141003 MGI PMID:12050119 1615193 Hoxd11 homeobox D11 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12050119 1615193 Hoxd11 homeobox D11 gene MP:0011565 kidney papillary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7596412 1615193 Hoxd11 homeobox D11 gene MP:0014320 abnormal autopod rotation IAGP N RGD:5509061 20240404 MGI PMID:7596412 1615194 Hoxa6 homeobox A6 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615194 Hoxa6 homeobox A6 gene MP:0000155 asymmetric rib joints IAGP N RGD:5509061 20141003 MGI PMID:7918106 1615194 Hoxa6 homeobox A6 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:7918106 1615194 Hoxa6 homeobox A6 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615194 Hoxa6 homeobox A6 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7918106 1615194 Hoxa6 homeobox A6 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615194 Hoxa6 homeobox A6 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615194 Hoxa6 homeobox A6 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615194 Hoxa6 homeobox A6 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615194 Hoxa6 homeobox A6 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615194 Hoxa6 homeobox A6 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7918106 1615194 Hoxa6 homeobox A6 gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615194 Hoxa6 homeobox A6 gene MP:0004680 small xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615194 Hoxa6 homeobox A6 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615194 Hoxa6 homeobox A6 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:17626057 1615196 Fbrs fibrosin gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 1615196 Fbrs fibrosin gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1615196 Fbrs fibrosin gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1615196 Fbrs fibrosin gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 1615196 Fbrs fibrosin gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20231207 MGI 1615196 Fbrs fibrosin gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1615196 Fbrs fibrosin gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20231207 MGI 1615196 Fbrs fibrosin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1615200 Fasn fatty acid synthase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17694178 1615200 Fasn fatty acid synthase gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:17694178 1615200 Fasn fatty acid synthase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17694178 1615200 Fasn fatty acid synthase gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16054078 1615200 Fasn fatty acid synthase gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17694178 1615200 Fasn fatty acid synthase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16054078 1615200 Fasn fatty acid synthase gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17694178 1615200 Fasn fatty acid synthase gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:16054078 1615200 Fasn fatty acid synthase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16054078 1615200 Fasn fatty acid synthase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16054078 1615200 Fasn fatty acid synthase gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17694178 1615200 Fasn fatty acid synthase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16054078 1615200 Fasn fatty acid synthase gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17694178 1615200 Fasn fatty acid synthase gene MP:0005286 decreased saturated fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16054078 1615200 Fasn fatty acid synthase gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17694178 1615200 Fasn fatty acid synthase gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16054078 1615200 Fasn fatty acid synthase gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17694178 1615200 Fasn fatty acid synthase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16054078 1615200 Fasn fatty acid synthase gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20141003 MGI PMID:17694178 1615200 Fasn fatty acid synthase gene MP:0006204 embryonic lethality before implantation IAGP N RGD:5509061 20141003 MGI PMID:12738878 1615200 Fasn fatty acid synthase gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16054078 1615200 Fasn fatty acid synthase gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16054078 1615200 Fasn fatty acid synthase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16054078 1615200 Fasn fatty acid synthase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17694178 1615200 Fasn fatty acid synthase gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16054078 1615200 Fasn fatty acid synthase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16054078 1615200 Fasn fatty acid synthase gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12738878 1615200 Fasn fatty acid synthase gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12738878 1615200 Fasn fatty acid synthase gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:17694178 1615200 Fasn fatty acid synthase gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:17694178 1615201 Cys1 cystin 1 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:1952600 1615201 Cys1 cystin 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:3404974 1615201 Cys1 cystin 1 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:11004214 1615201 Cys1 cystin 1 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:17148658 1615201 Cys1 cystin 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8800407 1615201 Cys1 cystin 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:6624875 1615201 Cys1 cystin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11004214 1615201 Cys1 cystin 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:6624875 1615201 Cys1 cystin 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:7062441 1615201 Cys1 cystin 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:4032601 1615201 Cys1 cystin 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8800407 1615201 Cys1 cystin 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:17148658 1615201 Cys1 cystin 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8800407 1615201 Cys1 cystin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:6624875 1615201 Cys1 cystin 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:4032601 1615201 Cys1 cystin 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:11004214 1615201 Cys1 cystin 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:18829740 1615201 Cys1 cystin 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:3404974 1615201 Cys1 cystin 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:4032601 1615201 Cys1 cystin 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:6624875 1615201 Cys1 cystin 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:7062441 1615201 Cys1 cystin 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:8800407 1615201 Cys1 cystin 1 gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20141003 MGI PMID:11004214 1615201 Cys1 cystin 1 gene MP:0003266 biliary cyst IAGP N RGD:5509061 20141003 MGI PMID:11004214 1615201 Cys1 cystin 1 gene MP:0003266 biliary cyst IAGP N RGD:5509061 20141003 MGI PMID:8800407 1615201 Cys1 cystin 1 gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:11004214 1615201 Cys1 cystin 1 gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:8800407 1615201 Cys1 cystin 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11004214 1615201 Cys1 cystin 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:4032601 1615201 Cys1 cystin 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:8800407 1615201 Cys1 cystin 1 gene MP:0003334 pancreas fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11004214 1615201 Cys1 cystin 1 gene MP:0003334 pancreas fibrosis IAGP N RGD:5509061 20141003 MGI PMID:4032601 1615201 Cys1 cystin 1 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:17148658 1615201 Cys1 cystin 1 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:8800407 1615201 Cys1 cystin 1 gene MP:0003637 cochlear ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:1952600 1615201 Cys1 cystin 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:11004214 1615201 Cys1 cystin 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17148658 1615201 Cys1 cystin 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18829740 1615201 Cys1 cystin 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:3404974 1615201 Cys1 cystin 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:4032601 1615201 Cys1 cystin 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:6624875 1615201 Cys1 cystin 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:7062441 1615201 Cys1 cystin 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:8800407 1615201 Cys1 cystin 1 gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1952600 1615201 Cys1 cystin 1 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:17148658 1615201 Cys1 cystin 1 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:18829740 1615201 Cys1 cystin 1 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:3404974 1615201 Cys1 cystin 1 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:4032601 1615201 Cys1 cystin 1 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1952600 1615201 Cys1 cystin 1 gene MP:0004403 absent cochlear outer hair cells IAGP N RGD:5509061 20141003 MGI PMID:1952600 1615201 Cys1 cystin 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:4032601 1615201 Cys1 cystin 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:6624875 1615201 Cys1 cystin 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:7062441 1615201 Cys1 cystin 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:4032601 1615201 Cys1 cystin 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:6624875 1615201 Cys1 cystin 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:11004214 1615201 Cys1 cystin 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18829740 1615201 Cys1 cystin 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:3404974 1615201 Cys1 cystin 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:4032601 1615201 Cys1 cystin 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:6624875 1615201 Cys1 cystin 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:7062441 1615201 Cys1 cystin 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:8800407 1615201 Cys1 cystin 1 gene MP:0006021 abnormal Reissner membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:1952600 1615201 Cys1 cystin 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20111116 MGI 1615201 Cys1 cystin 1 gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:11004214 1615201 Cys1 cystin 1 gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20141003 MGI PMID:4032601 1615201 Cys1 cystin 1 gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:4032601 1615201 Cys1 cystin 1 gene MP:0009157 ectopic pancreatic acinar cells IAGP N RGD:5509061 20141003 MGI PMID:4032601 1615201 Cys1 cystin 1 gene MP:0009173 absent pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:11004214 1615201 Cys1 cystin 1 gene MP:0009173 absent pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:4032601 1615201 Cys1 cystin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7062441 1615201 Cys1 cystin 1 gene MP:0011376 abnormal kidney corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:7062441 1615201 Cys1 cystin 1 gene MP:0011413 colorless urine IAGP N RGD:5509061 20141003 MGI PMID:6624875 1615201 Cys1 cystin 1 gene MP:0011413 colorless urine IAGP N RGD:5509061 20141003 MGI PMID:7062441 1615201 Cys1 cystin 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:1952600 1615203 Cox7c cytochrome c oxidase subunit 7C gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160421 MGI 1615203 Cox7c cytochrome c oxidase subunit 7C gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20201231 MGI 1615203 Cox7c cytochrome c oxidase subunit 7C gene MP:0001712 abnormal placenta development IEA N RGD:5509061 20201231 MGI 1615203 Cox7c cytochrome c oxidase subunit 7C gene MP:0002080 prenatal lethality IEA N RGD:5509061 20210520 MGI 1615203 Cox7c cytochrome c oxidase subunit 7C gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1615203 Cox7c cytochrome c oxidase subunit 7C gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1615203 Cox7c cytochrome c oxidase subunit 7C gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20160811 MGI 1615203 Cox7c cytochrome c oxidase subunit 7C gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20201231 MGI 1615203 Cox7c cytochrome c oxidase subunit 7C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615203 Cox7c cytochrome c oxidase subunit 7C gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20160421 MGI 1615203 Cox7c cytochrome c oxidase subunit 7C gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1615204 Cox7a1 cytochrome c oxidase subunit 7A1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22119795 1615204 Cox7a1 cytochrome c oxidase subunit 7A1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:22119795 1615204 Cox7a1 cytochrome c oxidase subunit 7A1 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:22119795 1615204 Cox7a1 cytochrome c oxidase subunit 7A1 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22119795 1615204 Cox7a1 cytochrome c oxidase subunit 7A1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:22119795 1615205 Cox17 cytochrome c oxidase assembly protein 17, copper chaperone gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12370308 1615205 Cox17 cytochrome c oxidase assembly protein 17, copper chaperone gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12370308 1615205 Cox17 cytochrome c oxidase assembly protein 17, copper chaperone gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:12370308 1615205 Cox17 cytochrome c oxidase assembly protein 17, copper chaperone gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12370308 1615206 Crisp3 cysteine-rich secretory protein 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230601 MGI 1615209 Adh5 alcohol dehydrogenase 5 (class III), chi polypeptide gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1615209 Adh5 alcohol dehydrogenase 5 (class III), chi polypeptide gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20160421 MGI 1615209 Adh5 alcohol dehydrogenase 5 (class III), chi polypeptide gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:14980227 1615209 Adh5 alcohol dehydrogenase 5 (class III), chi polypeptide gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:14980227 1615209 Adh5 alcohol dehydrogenase 5 (class III), chi polypeptide gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220519 MGI 1615209 Adh5 alcohol dehydrogenase 5 (class III), chi polypeptide gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:14980227 1615209 Adh5 alcohol dehydrogenase 5 (class III), chi polypeptide gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:14980227 1615209 Adh5 alcohol dehydrogenase 5 (class III), chi polypeptide gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10358022 1615209 Adh5 alcohol dehydrogenase 5 (class III), chi polypeptide gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21385828 1615209 Adh5 alcohol dehydrogenase 5 (class III), chi polypeptide gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:14980227 1615209 Adh5 alcohol dehydrogenase 5 (class III), chi polypeptide gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21385828 1615229 Mir33 microRNA 33 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20855588 1615229 Mir33 microRNA 33 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20855588 1615229 Mir33 microRNA 33 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20855588 1615229 Mir33 microRNA 33 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20855588 1615233 Tas2r103 taste receptor, type 2, member 103 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1615378 Serpina3i serine (or cysteine) peptidase inhibitor, clade A, member 3I gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1615378 Serpina3i serine (or cysteine) peptidase inhibitor, clade A, member 3I gene MP:0001399 hyperactivity IEA N RGD:5509061 20230119 MGI 1615378 Serpina3i serine (or cysteine) peptidase inhibitor, clade A, member 3I gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230119 MGI 1615378 Serpina3i serine (or cysteine) peptidase inhibitor, clade A, member 3I gene MP:0010052 increased grip strength IEA N RGD:5509061 20230119 MGI 1615419 Ripply1 ripply transcriptional repressor 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:20346937 1615419 Ripply1 ripply transcriptional repressor 1 gene MP:0000140 absent vertebral pedicles IAGP N RGD:5509061 20141003 MGI PMID:20346937 1615419 Ripply1 ripply transcriptional repressor 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:20346937 1615419 Ripply1 ripply transcriptional repressor 1 gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:20346937 1615422 Arhgef26 Rho guanine nucleotide exchange factor 26 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23372835 1615422 Arhgef26 Rho guanine nucleotide exchange factor 26 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:23372835 1615422 Arhgef26 Rho guanine nucleotide exchange factor 26 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23372835 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20221215 MGI 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20210429 MGI PMID:30877126 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20210429 MGI PMID:30877126 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210429 MGI PMID:30877126 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20210429 MGI PMID:30877126 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20181227 MGI 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20210429 MGI PMID:30877126 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0001925 male infertility IAGP N RGD:5509061 20210429 MGI PMID:30877126 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0001926 female infertility IAGP N RGD:5509061 20210429 MGI PMID:30877126 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20210429 MGI PMID:30877126 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20210429 MGI PMID:30877126 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20210429 MGI PMID:30877126 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20210429 MGI PMID:30877126 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20181227 MGI 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20210429 MGI PMID:30877126 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0011644 abnormal oviduct epithelium motile cilium morphology IAGP N RGD:5509061 20210429 MGI PMID:30877126 1615424 Mcidas multiciliate differentiation and DNA synthesis associated cell cycle protein gene MP:0013206 abnormal motile cilium morphology IAGP N RGD:5509061 20210429 MGI PMID:30877126 1615446 Mterf1a mitochondrial transcription termination factor 1a gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:23562081 1615449 Chrna10 cholinergic receptor, nicotinic, alpha polypeptide 10 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18077337 1615449 Chrna10 cholinergic receptor, nicotinic, alpha polypeptide 10 gene MP:0004432 abnormal cochlear hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18077337 1615449 Chrna10 cholinergic receptor, nicotinic, alpha polypeptide 10 gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18077337 1615449 Chrna10 cholinergic receptor, nicotinic, alpha polypeptide 10 gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18077337 1615449 Chrna10 cholinergic receptor, nicotinic, alpha polypeptide 10 gene MP:0004632 abnormal cochlear OHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:18077337 1615449 Chrna10 cholinergic receptor, nicotinic, alpha polypeptide 10 gene MP:0004633 abnormal cochlear IHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:18077337 1615449 Chrna10 cholinergic receptor, nicotinic, alpha polypeptide 10 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:18077337 1615450 Acd adrenocortical dysplasia gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0000416 sparse hair IEA N RGD:5509061 20111116 MGI 1615450 Acd adrenocortical dysplasia gene MP:0000424 retarded hair growth IEA N RGD:5509061 20111116 MGI 1615450 Acd adrenocortical dysplasia gene MP:0000562 polydactyly IEA N RGD:5509061 20111116 MGI 1615450 Acd adrenocortical dysplasia gene MP:0000585 kinked tail IEA N RGD:5509061 20111116 MGI 1615450 Acd adrenocortical dysplasia gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8014601 1615450 Acd adrenocortical dysplasia gene MP:0000640 adrenal gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8014601 1615450 Acd adrenocortical dysplasia gene MP:0000648 absent sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0001188 hyperpigmentation IEA N RGD:5509061 20111116 MGI 1615450 Acd adrenocortical dysplasia gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0001274 curly vibrissae IEA N RGD:5509061 20111116 MGI 1615450 Acd adrenocortical dysplasia gene MP:0001282 short vibrissae IEA N RGD:5509061 20111116 MGI 1615450 Acd adrenocortical dysplasia gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0001921 reduced fertility IEA N RGD:5509061 20111116 MGI 1615450 Acd adrenocortical dysplasia gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0002074 abnormal hair texture IEA N RGD:5509061 20111116 MGI 1615450 Acd adrenocortical dysplasia gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 1615450 Acd adrenocortical dysplasia gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20111116 MGI 1615450 Acd adrenocortical dysplasia gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:8014601 1615450 Acd adrenocortical dysplasia gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:8014601 1615450 Acd adrenocortical dysplasia gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:19995905 1615450 Acd adrenocortical dysplasia gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0003745 abnormal oral mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:8014601 1615450 Acd adrenocortical dysplasia gene MP:0003965 abnormal pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:8014601 1615450 Acd adrenocortical dysplasia gene MP:0003966 abnormal adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:8014601 1615450 Acd adrenocortical dysplasia gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:19995905 1615450 Acd adrenocortical dysplasia gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0005129 increased adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:8014601 1615450 Acd adrenocortical dysplasia gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19995905 1615450 Acd adrenocortical dysplasia gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:19995905 1615450 Acd adrenocortical dysplasia gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19995905 1615450 Acd adrenocortical dysplasia gene MP:0011276 increased tail pigmentation IEA N RGD:5509061 20170803 MGI 1615450 Acd adrenocortical dysplasia gene MP:0011278 increased ear pigmentation IEA N RGD:5509061 20170803 MGI 1615450 Acd adrenocortical dysplasia gene MP:0030926 increased skin pigmentation IAGP N RGD:5509061 20190117 MGI PMID:20493811 1615450 Acd adrenocortical dysplasia gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:20493811 1615456 Try10 trypsin 10 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1615456 Try10 trypsin 10 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210520 MGI 1615456 Try10 trypsin 10 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1615456 Try10 trypsin 10 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210520 MGI 1615456 Try10 trypsin 10 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210826 MGI 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0000434 megacephaly IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0001872 sinus inflammation IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0001893 non-obstructive hydrocephaly IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0002083 premature death IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0002766 situs inversus IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0005388 respiratory system phenotype IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0011649 immotile respiratory cilia IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615463 Dnaaf5 dynein, axonemal assembly factor 5 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20240111 MGI PMID:37104040 1615465 Fam222a family with sequence similarity 222, member A gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1615465 Fam222a family with sequence similarity 222, member A gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 1615465 Fam222a family with sequence similarity 222, member A gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1615466 Mn1 meningioma 1 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0000099 absent vomer bone IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0004424 temporal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0004450 presphenoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0004455 pterygoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0004458 absent alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0004460 alisphenoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0004461 basisphenoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0004899 absent temporal bone squamous part IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0009892 palate bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0009896 palatine bone horizontal plate hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0009898 maxillary shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0009900 vomer bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0030275 thin frontal bone IAGP N RGD:5509061 20171102 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0030277 thin interparietal bone IAGP N RGD:5509061 20171102 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0030281 thin parietal bone IAGP N RGD:5509061 20171102 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0030432 large cranial foramen ovale IAGP N RGD:5509061 20171214 MGI PMID:15870292 1615466 Mn1 meningioma 1 gene MP:0030433 large foramen rotundum IAGP N RGD:5509061 20171214 MGI PMID:15870292 1615472 Vrtn vertebrae development associated gene MP:0000160 kyphosis IAGP N RGD:5509061 20181101 MGI PMID:29904281 1615472 Vrtn vertebrae development associated gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20181101 MGI PMID:29904281 1615472 Vrtn vertebrae development associated gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20181101 MGI PMID:29904281 1615472 Vrtn vertebrae development associated gene MP:0003345 decreased rib number IAGP N RGD:5509061 20181101 MGI PMID:29904281 1615472 Vrtn vertebrae development associated gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20181101 MGI PMID:29904281 1615472 Vrtn vertebrae development associated gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20181101 MGI PMID:29904281 1615472 Vrtn vertebrae development associated gene MP:0004648 decreased thoracic vertebrae number IAGP N RGD:5509061 20181101 MGI PMID:29904281 1615472 Vrtn vertebrae development associated gene MP:0009768 impaired somite development IAGP N RGD:5509061 20181101 MGI PMID:29904281 1615472 Vrtn vertebrae development associated gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20181101 MGI PMID:29904281 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20180322 MGI PMID:29045386 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0000226 abnormal mean corpuscular volume IAGP N RGD:5509061 20180322 MGI PMID:29045386 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180322 MGI PMID:29045386 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20180322 MGI PMID:29045386 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20160804 MGI 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180322 MGI PMID:29045386 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20180322 MGI PMID:29045386 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20180322 MGI PMID:29045386 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20180322 MGI PMID:29045386 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0010074 stomatocytosis IAGP N RGD:5509061 20180322 MGI PMID:29045386 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0010163 hemolysis IAGP N RGD:5509061 20180322 MGI PMID:29045386 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20180322 MGI PMID:29045386 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0020116 increased sphingosine level IAGP N RGD:5509061 20180322 MGI PMID:29045386 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0020117 decreased sphingosine level IAGP N RGD:5509061 20180322 MGI PMID:29045386 1615478 Mfsd2b MFSD2 lysolipid transporter B, sphingolipid gene MP:0031276 abnormal stress erythropoiesis IAGP N RGD:5509061 20210805 MGI PMID:29045386 1615480 Dnai2 dynein axonemal intermediate chain 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20240523 MGI 1615480 Dnai2 dynein axonemal intermediate chain 2 gene MP:0002766 situs inversus IEA N RGD:5509061 20170209 MGI 1615480 Dnai2 dynein axonemal intermediate chain 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1615480 Dnai2 dynein axonemal intermediate chain 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1615480 Dnai2 dynein axonemal intermediate chain 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1615480 Dnai2 dynein axonemal intermediate chain 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1615480 Dnai2 dynein axonemal intermediate chain 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1615480 Dnai2 dynein axonemal intermediate chain 2 gene MP:0011252 situs inversus totalis IEA N RGD:5509061 20170209 MGI 1615480 Dnai2 dynein axonemal intermediate chain 2 gene MP:0011649 immotile respiratory cilia IEA N RGD:5509061 20170209 MGI 1615480 Dnai2 dynein axonemal intermediate chain 2 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20240523 MGI 1615486 Pax6os1 paired box 6 opposite strand 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20220224 MGI 1615487 Mir142 microRNA 142 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20160331 MGI PMID:26327117 1615487 Mir142 microRNA 142 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20160331 MGI PMID:26327117 1615487 Mir142 microRNA 142 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20160331 MGI PMID:26327117 1615487 Mir142 microRNA 142 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20160331 MGI PMID:26327117 1615487 Mir142 microRNA 142 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20160331 MGI PMID:26327117 1615487 Mir142 microRNA 142 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20160331 MGI PMID:26327117 1615487 Mir142 microRNA 142 gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141016 MGI PMID:24361879 1615488 Mir133a-1 microRNA 133a-1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19015276 1615488 Mir133a-1 microRNA 133a-1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:19015276 1615489 Mir1a-1 microRNA 1a-1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0003898 abnormal QRS complex IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0004070 abnormal P wave IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0004122 abnormal sinus arrhythmia IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0010577 abnormal heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615489 Mir1a-1 microRNA 1a-1 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20141003 MGI PMID:24252873 1615500 Nova2 NOVA alternative splicing regulator 2 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16213216 1615500 Nova2 NOVA alternative splicing regulator 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16213216 1615500 Nova2 NOVA alternative splicing regulator 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16213216 1615501 Ceacam3 CEA cell adhesion molecule 3 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 1615501 Ceacam3 CEA cell adhesion molecule 3 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1615501 Ceacam3 CEA cell adhesion molecule 3 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1615511 Lmtk3 lemur tyrosine kinase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151119 MGI PMID:24760852 1615511 Lmtk3 lemur tyrosine kinase 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20151119 MGI PMID:24760852 1615511 Lmtk3 lemur tyrosine kinase 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20151119 MGI PMID:24760852 1615511 Lmtk3 lemur tyrosine kinase 3 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20151119 MGI PMID:24760852 1615511 Lmtk3 lemur tyrosine kinase 3 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20151119 MGI PMID:24760852 1615511 Lmtk3 lemur tyrosine kinase 3 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20151119 MGI PMID:24760852 1615511 Lmtk3 lemur tyrosine kinase 3 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20151119 MGI PMID:24760852 1615511 Lmtk3 lemur tyrosine kinase 3 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20151119 MGI PMID:24760852 1615511 Lmtk3 lemur tyrosine kinase 3 gene MP:0003063 increased coping response IAGP N RGD:5509061 20151119 MGI PMID:24760852 1615511 Lmtk3 lemur tyrosine kinase 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20151119 MGI PMID:24760852 1615511 Lmtk3 lemur tyrosine kinase 3 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20151119 MGI PMID:24760852 1615511 Lmtk3 lemur tyrosine kinase 3 gene MP:0011939 increased food intake IAGP N RGD:5509061 20151119 MGI PMID:24760852 1615511 Lmtk3 lemur tyrosine kinase 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:24760852 1615517 Itgad integrin, alpha D gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15210787 1615517 Itgad integrin, alpha D gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:18097061 1615517 Itgad integrin, alpha D gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:18097061 1615517 Itgad integrin, alpha D gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:15210787 1615517 Itgad integrin, alpha D gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18097061 1615517 Itgad integrin, alpha D gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18097061 1615517 Itgad integrin, alpha D gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:15210787 1615517 Itgad integrin, alpha D gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:18097061 1615517 Itgad integrin, alpha D gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:18097061 1615517 Itgad integrin, alpha D gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15210787 1615517 Itgad integrin, alpha D gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15210787 1615517 Itgad integrin, alpha D gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15210787 1615517 Itgad integrin, alpha D gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:18097061 1615521 Cnrip1 cannabinoid receptor interacting protein 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1615521 Cnrip1 cannabinoid receptor interacting protein 1 gene MP:0005407 hyperalgesia IEA N RGD:5509061 20230720 MGI 1615523 Lin28b lin-28 homolog B gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:23666760 1615523 Lin28b lin-28 homolog B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23666760 1615523 Lin28b lin-28 homolog B gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1615523 Lin28b lin-28 homolog B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23666760 1615523 Lin28b lin-28 homolog B gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1615523 Lin28b lin-28 homolog B gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:23666760 1615523 Lin28b lin-28 homolog B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23666760 1615523 Lin28b lin-28 homolog B gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23666760 1615523 Lin28b lin-28 homolog B gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23666760 1615523 Lin28b lin-28 homolog B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23666760 1615523 Lin28b lin-28 homolog B gene MP:0012681 collapsed brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:23666760 1615524 Lemd3 LEM domain containing 3 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:16943282 1615524 Lemd3 LEM domain containing 3 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:16943282 1615524 Lemd3 LEM domain containing 3 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 1615524 Lemd3 LEM domain containing 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1615524 Lemd3 LEM domain containing 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1615524 Lemd3 LEM domain containing 3 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:16943282 1615524 Lemd3 LEM domain containing 3 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16943282 1615524 Lemd3 LEM domain containing 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16943282 1615524 Lemd3 LEM domain containing 3 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16943282 1615524 Lemd3 LEM domain containing 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1615524 Lemd3 LEM domain containing 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16943282 1615524 Lemd3 LEM domain containing 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1615524 Lemd3 LEM domain containing 3 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16943282 1615524 Lemd3 LEM domain containing 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0000440 domed cranium IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0001925 male infertility IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0002083 premature death IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0011057 absent brain ependyma motile cilia IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615526 Cfap54 cilia and flagella associated protein 54 gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20170126 MGI PMID:26224312 1615528 Heca hdc homolog, cell cycle regulator gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1615528 Heca hdc homolog, cell cycle regulator gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1615528 Heca hdc homolog, cell cycle regulator gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 1615528 Heca hdc homolog, cell cycle regulator gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1615529 Fastkd5 FAST kinase domains 5 gene MP:0001523 impaired righting response IEA N RGD:5509061 20181227 MGI 1615529 Fastkd5 FAST kinase domains 5 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191128 MGI 1615529 Fastkd5 FAST kinase domains 5 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1615529 Fastkd5 FAST kinase domains 5 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191128 MGI 1615529 Fastkd5 FAST kinase domains 5 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1615529 Fastkd5 FAST kinase domains 5 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191128 MGI 1615529 Fastkd5 FAST kinase domains 5 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20221215 MGI 1615529 Fastkd5 FAST kinase domains 5 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191128 MGI 1615529 Fastkd5 FAST kinase domains 5 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20210128 MGI 1615529 Fastkd5 FAST kinase domains 5 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1615529 Fastkd5 FAST kinase domains 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615529 Fastkd5 FAST kinase domains 5 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20170504 MGI 1615529 Fastkd5 FAST kinase domains 5 gene MP:0012724 absent head fold IEA N RGD:5509061 20191128 MGI 1615529 Fastkd5 FAST kinase domains 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191128 MGI 1615529 Fastkd5 FAST kinase domains 5 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1615531 Rnu11 U11 small nuclear RNA gene MP:0000433 microcephaly IAGP N RGD:5509061 20200402 MGI PMID:30093551 1615531 Rnu11 U11 small nuclear RNA gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20200402 MGI PMID:30093551 1615531 Rnu11 U11 small nuclear RNA gene MP:0004171 abnormal pallium development IAGP N RGD:5509061 20200402 MGI PMID:30093551 1615531 Rnu11 U11 small nuclear RNA gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20200402 MGI PMID:30093551 1615531 Rnu11 U11 small nuclear RNA gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20200402 MGI PMID:30093551 1615531 Rnu11 U11 small nuclear RNA gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200402 MGI PMID:30093551 1615531 Rnu11 U11 small nuclear RNA gene MP:0012556 increased cell death IAGP N RGD:5509061 20200402 MGI PMID:30093551 1615531 Rnu11 U11 small nuclear RNA gene MP:0020388 decreased radial glial cell number IAGP N RGD:5509061 20200402 MGI PMID:30093551 1615538 Cd59b CD59b antigen gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0000256 echinocytosis IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0000314 schistocytosis IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0000315 hemoglobinuria IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0000327 hemosiderinuria IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0000332 hemoglobinemia IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16272280 1615538 Cd59b CD59b antigen gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16272280 1615538 Cd59b CD59b antigen gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0005096 erythroblastosis IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:16272280 1615538 Cd59b CD59b antigen gene MP:0009234 absent sperm head IAGP N RGD:5509061 20141003 MGI PMID:16272280 1615538 Cd59b CD59b antigen gene MP:0009325 necrospermia IAGP N RGD:5509061 20141003 MGI PMID:16272280 1615538 Cd59b CD59b antigen gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:16272280 1615538 Cd59b CD59b antigen gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:12594949 1615538 Cd59b CD59b antigen gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:16272280 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16862125 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17486093 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17187069 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17486093 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:17187069 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17187069 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17486093 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18776906 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17486093 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:16862125 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0008691 decreased interleukin-23 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:17187069 1615540 Card9 caspase recruitment domain family, member 9 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:18776906 1615544 Spata21 spermatogenesis associated 21 gene MP:0001513 limb grasping IEA N RGD:5509061 20231207 MGI 1615544 Spata21 spermatogenesis associated 21 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1615545 Catsper4 cation channel, sperm associated 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17227845 1615545 Catsper4 cation channel, sperm associated 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17344468 1615545 Catsper4 cation channel, sperm associated 4 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:17227845 1615545 Catsper4 cation channel, sperm associated 4 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:17344468 1615545 Catsper4 cation channel, sperm associated 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17227845 1615545 Catsper4 cation channel, sperm associated 4 gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20141003 MGI PMID:17227845 1615545 Catsper4 cation channel, sperm associated 4 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:17227845 1615545 Catsper4 cation channel, sperm associated 4 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17227845 1615547 Foxo6 forkhead box O6 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23222102 1615547 Foxo6 forkhead box O6 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:23222102 1615547 Foxo6 forkhead box O6 gene MP:0001468 abnormal temporal memory IAGP N RGD:5509061 20141003 MGI PMID:23222102 1615547 Foxo6 forkhead box O6 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:23222102 1615547 Foxo6 forkhead box O6 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20170223 MGI PMID:25944898 1615547 Foxo6 forkhead box O6 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:23222102 1615547 Foxo6 forkhead box O6 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20211014 MGI PMID:23222102 1615547 Foxo6 forkhead box O6 gene MP:0020510 increased dendritic spine length IAGP N RGD:5509061 20211014 MGI PMID:23222102 1615547 Foxo6 forkhead box O6 gene MP:0021018 decreased dendritic spine number IAGP N RGD:5509061 20211014 MGI PMID:23222102 1615547 Foxo6 forkhead box O6 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:25944898 1615548 Skint2 selection and upkeep of intraepithelial T cells 2 gene MP:0013410 decreased dendritic epidermal T cell number IAGP N RGD:5509061 20231109 MGI PMID:32724083 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0011939 increased food intake IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20200310 MGI PMID:22427358 1615550 Acot11 acyl-CoA thioesterase 11 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:22427358 1615553 Bex6 brain expressed family member 6 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210520 MGI 1615553 Bex6 brain expressed family member 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20170105 MGI 1615553 Bex6 brain expressed family member 6 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 1615553 Bex6 brain expressed family member 6 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210520 MGI 1615560 Spata33 spermatogenesis associated 33 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220120 MGI PMID:34446558 1615560 Spata33 spermatogenesis associated 33 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220120 MGI PMID:34446558 1615560 Spata33 spermatogenesis associated 33 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20220120 MGI PMID:34446558 1615560 Spata33 spermatogenesis associated 33 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220120 MGI PMID:34446558 1615561 Cdh18 cadherin 18 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20230119 MGI 1615561 Cdh18 cadherin 18 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1615561 Cdh18 cadherin 18 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20240523 MGI 1615561 Cdh18 cadherin 18 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1615561 Cdh18 cadherin 18 gene MP:0002183 gliosis IAGP N RGD:5509061 20180201 MGI PMID:12105373 1615561 Cdh18 cadherin 18 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20180201 MGI PMID:12105373 1615561 Cdh18 cadherin 18 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20180201 MGI PMID:10514484 1615562 Krt26 keratin 26 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1615562 Krt26 keratin 26 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230601 MGI 1615562 Krt26 keratin 26 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20230601 MGI 1615562 Krt26 keratin 26 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20230601 MGI 1615564 Sirpb1a signal-regulatory protein beta 1A gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1615565 Atad2b ATPase family, AAA domain containing 2B gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210826 MGI 1615565 Atad2b ATPase family, AAA domain containing 2B gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1615565 Atad2b ATPase family, AAA domain containing 2B gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1615565 Atad2b ATPase family, AAA domain containing 2B gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1615565 Atad2b ATPase family, AAA domain containing 2B gene MP:0001469 abnormal contextual conditioning behavior IEA N RGD:5509061 20210128 MGI 1615565 Atad2b ATPase family, AAA domain containing 2B gene MP:0001923 reduced female fertility IEA N RGD:5509061 20111116 MGI 1615565 Atad2b ATPase family, AAA domain containing 2B gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20201231 MGI 1615565 Atad2b ATPase family, AAA domain containing 2B gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20160811 MGI 1615565 Atad2b ATPase family, AAA domain containing 2B gene MP:0004357 long tibia IEA N RGD:5509061 20160421 MGI 1615565 Atad2b ATPase family, AAA domain containing 2B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1615565 Atad2b ATPase family, AAA domain containing 2B gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20170105 MGI 1615565 Atad2b ATPase family, AAA domain containing 2B gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20211021 MGI 1615568 Xkr5 X-linked Kx blood group related 5 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1615568 Xkr5 X-linked Kx blood group related 5 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1615569 Defb20 defensin beta 20 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1615569 Defb20 defensin beta 20 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20160204 MGI PMID:24586179 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20160204 MGI PMID:24586179 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:17267447 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17267447 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:18477613 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20160204 MGI PMID:24586179 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17267447 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20141003 MGI PMID:17267447 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18477613 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0002864 abnormal ocular fundus morphology IEA N RGD:5509061 20190912 MGI 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18477613 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20160204 MGI PMID:24586179 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20160630 MGI PMID:26066746 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20160204 MGI PMID:24586179 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20160204 MGI PMID:24586179 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0003728 abnormal retina photoreceptor layer morphology IEA N RGD:5509061 20190912 MGI 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20160630 MGI PMID:26066746 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220811 MGI 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20160630 MGI PMID:26066746 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20160630 MGI PMID:26066746 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0004857 abnormal heart weight IAGP N RGD:5509061 20160204 MGI PMID:24586179 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160204 MGI PMID:24586179 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20160630 MGI PMID:26066746 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20160630 MGI PMID:26066746 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20160630 MGI PMID:26066746 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20160630 MGI PMID:26066746 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20160630 MGI PMID:26066746 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20160630 MGI PMID:26066746 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20160630 MGI PMID:26066746 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20160630 MGI PMID:26066746 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20160630 MGI PMID:26066746 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20160630 MGI PMID:26066746 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20190912 MGI 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17267447 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:18477613 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20190912 MGI 1615570 Syne2 spectrin repeat containing, nuclear envelope 2 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:26066746 1615573 Spx spexin hormone gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 1615574 Zfp182 zinc finger protein 182 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1615574 Zfp182 zinc finger protein 182 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160211 MGI 1615574 Zfp182 zinc finger protein 182 gene MP:0001304 cataract IEA N RGD:5509061 20160211 MGI 1615575 Zfp750 zinc finger protein 750 gene MP:0001196 shiny skin IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0001263 weight loss IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0001341 absent eyelids IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0001429 dehydration IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0009596 abnormal stratum corneum lipid matrix formation IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0009607 decreased keratohyalin granule size IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0011006 abnormal epidermal stem cell proliferation IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1615575 Zfp750 zinc finger protein 750 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615575 Zfp750 zinc finger protein 750 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20230601 MGI PMID:37115925 1615579 Slc9a5 solute carrier family 9 (sodium/hydrogen exchanger), member 5 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20210318 MGI PMID:28981195 1615579 Slc9a5 solute carrier family 9 (sodium/hydrogen exchanger), member 5 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20210318 MGI PMID:28981195 1615579 Slc9a5 solute carrier family 9 (sodium/hydrogen exchanger), member 5 gene MP:0003999 enhanced passive avoidance behavior IAGP N RGD:5509061 20210318 MGI PMID:28981195 1615579 Slc9a5 solute carrier family 9 (sodium/hydrogen exchanger), member 5 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1615579 Slc9a5 solute carrier family 9 (sodium/hydrogen exchanger), member 5 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20210318 MGI PMID:28981195 1615579 Slc9a5 solute carrier family 9 (sodium/hydrogen exchanger), member 5 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20210318 MGI PMID:28981195 1615579 Slc9a5 solute carrier family 9 (sodium/hydrogen exchanger), member 5 gene MP:0012314 enhanced learning IAGP N RGD:5509061 20210318 MGI PMID:28981195 1615581 Ip6k3 inositol hexaphosphate kinase 3 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20160915 MGI PMID:26245967 1615581 Ip6k3 inositol hexaphosphate kinase 3 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20160915 MGI PMID:26245967 1615581 Ip6k3 inositol hexaphosphate kinase 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160915 MGI PMID:26245967 1615581 Ip6k3 inositol hexaphosphate kinase 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160915 MGI PMID:26245967 1615581 Ip6k3 inositol hexaphosphate kinase 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20160915 MGI PMID:26245967 1615581 Ip6k3 inositol hexaphosphate kinase 3 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20160915 MGI PMID:26245967 1615581 Ip6k3 inositol hexaphosphate kinase 3 gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20160915 MGI PMID:26245967 1615581 Ip6k3 inositol hexaphosphate kinase 3 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20160915 MGI PMID:26245967 1615581 Ip6k3 inositol hexaphosphate kinase 3 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20160915 MGI PMID:26245967 1615581 Ip6k3 inositol hexaphosphate kinase 3 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20160915 MGI PMID:26245967 1615581 Ip6k3 inositol hexaphosphate kinase 3 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20160915 MGI PMID:26245967 1615581 Ip6k3 inositol hexaphosphate kinase 3 gene MP:0021018 decreased dendritic spine number IAGP N RGD:5509061 20211014 MGI PMID:26245967 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:22558334 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20160421 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20181227 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0000745 tremors IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20240523 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20201022 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:22558334 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20201022 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0001410 head bobbing IEA N RGD:5509061 20160421 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0001512 trunk curl IEA N RGD:5509061 20160421 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:22558334 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20160421 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220519 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:22558334 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20160421 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0003062 abnormal coping response IEA N RGD:5509061 20160804 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0003313 abnormal locomotor activation IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20201022 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20210128 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160421 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:22558334 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220519 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0005316 abnormal response to tactile stimuli IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20211021 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160804 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:22558334 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20141003 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0010511 shortened PR interval IEA N RGD:5509061 20201022 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0011954 shortened PQ interval IEA N RGD:5509061 20201022 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:22558334 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0012361 decreased large unstained cell number IEA N RGD:5509061 20201022 MGI 1615583 Elmod1 ELMO/CED-12 domain containing 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1615584 Pou2af3 POU class 2 homeobox associating factor 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230720 MGI 1615584 Pou2af3 POU class 2 homeobox associating factor 3 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20231207 MGI 1615584 Pou2af3 POU class 2 homeobox associating factor 3 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 1615584 Pou2af3 POU class 2 homeobox associating factor 3 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230720 MGI 1615584 Pou2af3 POU class 2 homeobox associating factor 3 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20231207 MGI 1615584 Pou2af3 POU class 2 homeobox associating factor 3 gene MP:0001925 male infertility IEA N RGD:5509061 20230720 MGI 1615584 Pou2af3 POU class 2 homeobox associating factor 3 gene MP:0002764 short tibia IEA N RGD:5509061 20230720 MGI 1615584 Pou2af3 POU class 2 homeobox associating factor 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 1615584 Pou2af3 POU class 2 homeobox associating factor 3 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20230720 MGI 1615584 Pou2af3 POU class 2 homeobox associating factor 3 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 1615584 Pou2af3 POU class 2 homeobox associating factor 3 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 1615584 Pou2af3 POU class 2 homeobox associating factor 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230720 MGI 1615584 Pou2af3 POU class 2 homeobox associating factor 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230720 MGI 1615584 Pou2af3 POU class 2 homeobox associating factor 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230720 MGI 1615584 Pou2af3 POU class 2 homeobox associating factor 3 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20230720 MGI 1615585 Nkapd1 NKAP domain containing 1 gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20220519 MGI 1615585 Nkapd1 NKAP domain containing 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210422 MGI 1615585 Nkapd1 NKAP domain containing 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1615585 Nkapd1 NKAP domain containing 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 1615585 Nkapd1 NKAP domain containing 1 gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20220519 MGI 1615585 Nkapd1 NKAP domain containing 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210422 MGI 1615585 Nkapd1 NKAP domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615585 Nkapd1 NKAP domain containing 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1615585 Nkapd1 NKAP domain containing 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240523 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20240523 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20240523 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20240523 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20240523 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20240523 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:21903076 1615587 Fat3 FAT atypical cadherin 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20240523 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20240523 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20230601 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20240523 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20240523 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21903076 1615587 Fat3 FAT atypical cadherin 3 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21903076 1615587 Fat3 FAT atypical cadherin 3 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21903076 1615587 Fat3 FAT atypical cadherin 3 gene MP:0008508 thick retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:21903076 1615587 Fat3 FAT atypical cadherin 3 gene MP:0010895 increased lung compliance IEA N RGD:5509061 20230601 MGI 1615587 Fat3 FAT atypical cadherin 3 gene MP:0011045 decreased lung elastance IEA N RGD:5509061 20230601 MGI 1615589 Irf2bp2 interferon regulatory factor 2 binding protein 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20160218 MGI PMID:26593974 1615589 Irf2bp2 interferon regulatory factor 2 binding protein 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160218 MGI PMID:26593974 1615589 Irf2bp2 interferon regulatory factor 2 binding protein 2 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20160218 MGI PMID:26593974 1615589 Irf2bp2 interferon regulatory factor 2 binding protein 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20160218 MGI PMID:26593974 1615589 Irf2bp2 interferon regulatory factor 2 binding protein 2 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20160218 MGI PMID:26593974 1615589 Irf2bp2 interferon regulatory factor 2 binding protein 2 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20160218 MGI PMID:26593974 1615589 Irf2bp2 interferon regulatory factor 2 binding protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160218 MGI PMID:26593974 1615589 Irf2bp2 interferon regulatory factor 2 binding protein 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20160218 MGI PMID:26593974 1615589 Irf2bp2 interferon regulatory factor 2 binding protein 2 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20160218 MGI PMID:26593974 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:22357600 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:22357600 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21623373 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22357600 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22357600 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22357600 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:21623373 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:21623373 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:21623373 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:21623373 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:21623373 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22357600 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21623373 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22357600 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22357600 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615591 Rbfox1 RNA binding protein, fox-1 homolog (C. elegans) 1 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20211014 MGI PMID:21623373 1615620 Il27 interleukin 27 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:19380822 1615620 Il27 interleukin 27 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:19380822 1615620 Il27 interleukin 27 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19380822 1615620 Il27 interleukin 27 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22981537 1615620 Il27 interleukin 27 gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:22981537 1615620 Il27 interleukin 27 gene MP:0010750 increased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22981537 1615620 Il27 interleukin 27 gene MP:0010836 decreased CD4-positive, alpha-beta memory T cell number IEA N RGD:5509061 20201022 MGI 1615620 Il27 interleukin 27 gene MP:0013433 increased KLRG1-positive CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1615621 Adig adipogenin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615621 Adig adipogenin gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615621 Adig adipogenin gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20231207 MGI 1615621 Adig adipogenin gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615621 Adig adipogenin gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615621 Adig adipogenin gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615621 Adig adipogenin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615621 Adig adipogenin gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615621 Adig adipogenin gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615621 Adig adipogenin gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615621 Adig adipogenin gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20221215 MGI 1615621 Adig adipogenin gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615621 Adig adipogenin gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615621 Adig adipogenin gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615621 Adig adipogenin gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615621 Adig adipogenin gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615621 Adig adipogenin gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615621 Adig adipogenin gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210708 MGI PMID:33691105 1615624 Defb19 defensin beta 19 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20230202 MGI PMID:36513070 1615624 Defb19 defensin beta 19 gene MP:0005410 abnormal fertilization IAGP N RGD:5509061 20230202 MGI PMID:36513070 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150806 MGI PMID:21241452 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:12400016 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12400016 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12400016 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:19391112 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12400016 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19391112 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18626023 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0003426 pulmonary interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0003674 oxidative stress IAGP N RGD:5509061 20150806 MGI PMID:21241452 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:12400016 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12400016 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20150806 MGI PMID:21241452 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20150806 MGI PMID:21241452 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19391112 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20150806 MGI PMID:21241452 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:18626023 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0009563 dyskeratosis IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0010384 increased renal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0010901 abnormal pulmonary alveolar parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12400016 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12400016 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20150806 MGI PMID:21241452 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0011903 decreased hematopoietic stem cell proliferation IAGP N RGD:5509061 20150806 MGI PMID:21241452 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0012119 increased trophectoderm apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12400016 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0012120 trophectoderm cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12400016 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0014473 increased pulmonary alveolus wall thickness IAGP N RGD:5509061 20240704 MGI PMID:12522253 1615626 Dkc1 dyskeratosis congenita 1, dyskerin gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:12522253 1615630 Tm9sf5 transmembrane 9 superfamily member 5 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20220811 MGI PMID:34635817 1615630 Tm9sf5 transmembrane 9 superfamily member 5 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220811 MGI PMID:34635817 1615630 Tm9sf5 transmembrane 9 superfamily member 5 gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20220811 MGI PMID:34635817 1615630 Tm9sf5 transmembrane 9 superfamily member 5 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220811 MGI PMID:34635817 1615630 Tm9sf5 transmembrane 9 superfamily member 5 gene MP:0003718 maternal effect IAGP N RGD:5509061 20220811 MGI PMID:34635817 1615630 Tm9sf5 transmembrane 9 superfamily member 5 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20220811 MGI PMID:34635817 1615630 Tm9sf5 transmembrane 9 superfamily member 5 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20220811 MGI PMID:34635817 1615630 Tm9sf5 transmembrane 9 superfamily member 5 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20220811 MGI PMID:34635817 1615630 Tm9sf5 transmembrane 9 superfamily member 5 gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20220811 MGI PMID:34635817 1615630 Tm9sf5 transmembrane 9 superfamily member 5 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220811 MGI PMID:34635817 1615630 Tm9sf5 transmembrane 9 superfamily member 5 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220811 MGI PMID:34635817 1615630 Tm9sf5 transmembrane 9 superfamily member 5 gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20220811 MGI PMID:34635817 1615630 Tm9sf5 transmembrane 9 superfamily member 5 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220811 MGI PMID:34635817 1615632 Ovch2 ovochymase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20201022 MGI PMID:32499443 1615632 Ovch2 ovochymase 2 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20201022 MGI PMID:32499443 1615632 Ovch2 ovochymase 2 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20201022 MGI PMID:32499443 1615635 Trim30b tripartite motif-containing 30B gene MP:0004357 long tibia IEA N RGD:5509061 20220811 MGI 1615636 Ubqln3 ubiquilin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1615636 Ubqln3 ubiquilin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25776854 1615637 Usp35 ubiquitin specific peptidase 35 gene MP:0003900 shortened QT interval IEA N RGD:5509061 20211021 MGI 1615637 Usp35 ubiquitin specific peptidase 35 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20230601 MGI 1615640 Napepld N-acyl phosphatidylethanolamine phospholipase D gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21801852 1615640 Napepld N-acyl phosphatidylethanolamine phospholipase D gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:16605240 1615640 Napepld N-acyl phosphatidylethanolamine phospholipase D gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:20393650 1615642 Gnat3 G protein subunit alpha transducin 3 gene MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:8657284 1615642 Gnat3 G protein subunit alpha transducin 3 gene MP:0004209 abnormal sweet taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:8657284 1615642 Gnat3 G protein subunit alpha transducin 3 gene MP:0004210 abnormal bitter taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:8657284 1615642 Gnat3 G protein subunit alpha transducin 3 gene MP:0004213 abnormal umami taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15342734 1615642 Gnat3 G protein subunit alpha transducin 3 gene MP:0005423 abnormal somatic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15342734 1615643 Lrrd1 leucine rich repeats and death domain containing 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38697008 1615644 Rundc3b RUN domain containing 3B gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1615644 Rundc3b RUN domain containing 3B gene MP:0002574 increased vertical activity IEA N RGD:5509061 20240523 MGI 1615644 Rundc3b RUN domain containing 3B gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20231207 MGI 1615644 Rundc3b RUN domain containing 3B gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20231207 MGI 1615645 Ankrd65 ankyrin repeat domain 65 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1615646 Lrrc4c leucine rich repeat containing 4C gene MP:0008596 increased circulating interleukin-6 level IEA N RGD:5509061 20200310 MGI 1615647 Lrrc55 leucine rich repeat containing 55 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20240530 MGI PMID:33346797 1615647 Lrrc55 leucine rich repeat containing 55 gene MP:0011445 abnormal renal protein reabsorption IAGP N RGD:5509061 20240530 MGI PMID:33346797 1615647 Lrrc55 leucine rich repeat containing 55 gene MP:0011863 abnormal podocyte physiology IAGP N RGD:5509061 20240530 MGI PMID:33346797 1615648 Ypel4 yippee like 4 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20220616 MGI PMID:34354145 1615648 Ypel4 yippee like 4 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20211021 MGI 1615648 Ypel4 yippee like 4 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20220616 MGI PMID:34354145 1615648 Ypel4 yippee like 4 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20220616 MGI PMID:34354145 1615648 Ypel4 yippee like 4 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20220616 MGI PMID:34354145 1615648 Ypel4 yippee like 4 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20220616 MGI PMID:34354145 1615648 Ypel4 yippee like 4 gene MP:0002872 polycythemia IAGP N RGD:5509061 20220616 MGI PMID:34354145 1615648 Ypel4 yippee like 4 gene MP:0009547 elliptocytosis IAGP N RGD:5509061 20220616 MGI PMID:34354145 1615648 Ypel4 yippee like 4 gene MP:0009568 abnormal red blood cell deformability IAGP N RGD:5509061 20220616 MGI PMID:34354145 1615648 Ypel4 yippee like 4 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 1615648 Ypel4 yippee like 4 gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20220616 MGI PMID:34354145 1615650 Fsip2 fibrous sheath-interacting protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20210805 MGI PMID:34125190 1615650 Fsip2 fibrous sheath-interacting protein 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210805 MGI PMID:34125190 1615650 Fsip2 fibrous sheath-interacting protein 2 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20210805 MGI PMID:34125190 1615650 Fsip2 fibrous sheath-interacting protein 2 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20210805 MGI PMID:34125190 1615650 Fsip2 fibrous sheath-interacting protein 2 gene MP:0009280 decreased activated sperm motility IAGP N RGD:5509061 20210805 MGI PMID:34125190 1615650 Fsip2 fibrous sheath-interacting protein 2 gene MP:0030591 absent sperm fibrous sheath IAGP N RGD:5509061 20210805 MGI PMID:34125190 1615653 Ythdc2 YTH domain containing 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1615653 Ythdc2 YTH domain containing 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20171102 MGI PMID:28809393 1615653 Ythdc2 YTH domain containing 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20210128 MGI PMID:29360036 1615653 Ythdc2 YTH domain containing 2 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20171102 MGI PMID:29033321 1615653 Ythdc2 YTH domain containing 2 gene MP:0001147 small testis IAGP N RGD:5509061 20171102 MGI PMID:28809393 1615653 Ythdc2 YTH domain containing 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20210128 MGI PMID:29360036 1615653 Ythdc2 YTH domain containing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20171102 MGI PMID:28809393 1615653 Ythdc2 YTH domain containing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20171102 MGI PMID:29033321 1615653 Ythdc2 YTH domain containing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20210128 MGI PMID:29360036 1615653 Ythdc2 YTH domain containing 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20171102 MGI PMID:28809393 1615653 Ythdc2 YTH domain containing 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20171102 MGI PMID:29033321 1615653 Ythdc2 YTH domain containing 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20210128 MGI PMID:29360036 1615653 Ythdc2 YTH domain containing 2 gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20171102 MGI PMID:28809393 1615653 Ythdc2 YTH domain containing 2 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20171102 MGI PMID:29033321 1615653 Ythdc2 YTH domain containing 2 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20210128 MGI 1615653 Ythdc2 YTH domain containing 2 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20171102 MGI PMID:29033321 1615653 Ythdc2 YTH domain containing 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1615653 Ythdc2 YTH domain containing 2 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20171102 MGI PMID:29033321 1615653 Ythdc2 YTH domain containing 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210128 MGI PMID:29360036 1615653 Ythdc2 YTH domain containing 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20171102 MGI PMID:28809393 1615653 Ythdc2 YTH domain containing 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20171102 MGI PMID:29033321 1615653 Ythdc2 YTH domain containing 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20210128 MGI PMID:29360036 1615653 Ythdc2 YTH domain containing 2 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20171102 MGI PMID:28809393 1615653 Ythdc2 YTH domain containing 2 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20171102 MGI PMID:29033321 1615653 Ythdc2 YTH domain containing 2 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20171102 MGI PMID:29033321 1615653 Ythdc2 YTH domain containing 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20171102 MGI PMID:28809393 1615653 Ythdc2 YTH domain containing 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20171102 MGI PMID:29033321 1615653 Ythdc2 YTH domain containing 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20210128 MGI PMID:29360036 1615653 Ythdc2 YTH domain containing 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1615653 Ythdc2 YTH domain containing 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1615653 Ythdc2 YTH domain containing 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20171102 MGI PMID:28809393 1615653 Ythdc2 YTH domain containing 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20171102 MGI PMID:29033321 1615653 Ythdc2 YTH domain containing 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20210128 MGI PMID:29360036 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22933801 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:22933801 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:19874790 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:22933801 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0002204 abnormal synaptic neurotransmitter level IAGP N RGD:5509061 20141003 MGI PMID:19874790 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:19874790 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19874790 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22933801 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22933801 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22933801 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:19874790 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22933801 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22933801 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22933801 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:22933801 1615655 Erc2 ELKS/RAB6-interacting/CAST family member 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:19874790 1615656 Nek10 NIMA (never in mitosis gene a)- related kinase 10 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20191128 MGI 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0000181 abnormal circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15671032 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15671032 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15671032 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15671032 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0002323 decreased susceptibility to hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:15671032 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0002645 abnormal intestinal cholesterol absorption IAGP N RGD:5509061 20151224 MGI PMID:24336247 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:14976318 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:15671032 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20180830 MGI PMID:29880681 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0005085 abnormal gallbladder physiology IAGP N RGD:5509061 20200116 MGI PMID:15671032 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15671032 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20151224 MGI PMID:24336247 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15671032 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:15671032 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15671032 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15671032 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20240627 MGI PMID:14976318 1615659 Npc1l1 NPC1 like intracellular cholesterol transporter 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:15671032 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0000753 paralysis IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:23626854 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20160915 MGI PMID:23626854 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20160915 MGI PMID:23626854 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:23626854 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0001506 limp posture IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20160915 MGI PMID:23626854 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20150723 MGI PMID:23626854 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0004246 abnormal extensor digitorum longus morphology IAGP N RGD:5509061 20141003 MGI PMID:23626854 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20160915 MGI PMID:23626854 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0004627 abnormal trochanter morphology IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0005039 hypoxia IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0005162 carpoptosis IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0006432 abnormal costal cartilage morphology IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20160915 MGI PMID:23626854 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20160915 MGI PMID:23626854 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20160915 MGI PMID:23626854 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:23626854 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23626854 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615660 Stac3 SH3 and cysteine rich domain 3 gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20160915 MGI PMID:23818578 1615664 Igsf9b immunoglobulin superfamily, member 9B gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20190502 MGI 1615664 Igsf9b immunoglobulin superfamily, member 9B gene MP:0001399 hyperactivity IEA N RGD:5509061 20200402 MGI 1615664 Igsf9b immunoglobulin superfamily, member 9B gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20240627 MGI 1615664 Igsf9b immunoglobulin superfamily, member 9B gene MP:0002574 increased vertical activity IEA N RGD:5509061 20200402 MGI 1615667 Zfp809 zinc finger protein 809 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20170518 MGI PMID:25737282 1615670 Atg4d autophagy related 4D, cysteine peptidase gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20211209 MGI PMID:33795848 1615670 Atg4d autophagy related 4D, cysteine peptidase gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20211209 MGI PMID:33795848 1615670 Atg4d autophagy related 4D, cysteine peptidase gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20211209 MGI PMID:33795848 1615670 Atg4d autophagy related 4D, cysteine peptidase gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20211209 MGI PMID:33795848 1615670 Atg4d autophagy related 4D, cysteine peptidase gene MP:0001393 ataxia IAGP N RGD:5509061 20211209 MGI PMID:33795848 1615670 Atg4d autophagy related 4D, cysteine peptidase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20211209 MGI PMID:33795848 1615670 Atg4d autophagy related 4D, cysteine peptidase gene MP:0001513 limb grasping IAGP N RGD:5509061 20211209 MGI PMID:33795848 1615670 Atg4d autophagy related 4D, cysteine peptidase gene MP:0002183 gliosis IAGP N RGD:5509061 20211209 MGI PMID:33795848 1615670 Atg4d autophagy related 4D, cysteine peptidase gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20211209 MGI PMID:33795848 1615670 Atg4d autophagy related 4D, cysteine peptidase gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20211209 MGI PMID:33795848 1615670 Atg4d autophagy related 4D, cysteine peptidase gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20211209 MGI PMID:33795848 1615670 Atg4d autophagy related 4D, cysteine peptidase gene MP:0010540 long stride length IAGP N RGD:5509061 20211209 MGI PMID:33795848 1615670 Atg4d autophagy related 4D, cysteine peptidase gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:33795848 1615670 Atg4d autophagy related 4D, cysteine peptidase gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20211209 MGI PMID:33795848 1615671 Rdh8 retinol dehydrogenase 8 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:19494204 1615671 Rdh8 retinol dehydrogenase 8 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:19494204 1615671 Rdh8 retinol dehydrogenase 8 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:19494204 1615671 Rdh8 retinol dehydrogenase 8 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20180614 MGI PMID:24712709 1615671 Rdh8 retinol dehydrogenase 8 gene MP:0003011 delayed dark adaptation IAGP N RGD:5509061 20141003 MGI PMID:15755727 1615671 Rdh8 retinol dehydrogenase 8 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19494204 1615671 Rdh8 retinol dehydrogenase 8 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19494204 1615671 Rdh8 retinol dehydrogenase 8 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:19494204 1615671 Rdh8 retinol dehydrogenase 8 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19494204 1615671 Rdh8 retinol dehydrogenase 8 gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:19494204 1615671 Rdh8 retinol dehydrogenase 8 gene MP:0005546 choroidal neovascularization IAGP N RGD:5509061 20220217 MGI PMID:19494204 1615671 Rdh8 retinol dehydrogenase 8 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19494204 1615671 Rdh8 retinol dehydrogenase 8 gene MP:0006187 retina deposits IAGP N RGD:5509061 20141003 MGI PMID:19494204 1615671 Rdh8 retinol dehydrogenase 8 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:19494204 1615671 Rdh8 retinol dehydrogenase 8 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:19494204 1615672 Acsm2 acyl-CoA synthetase medium-chain family member 2 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20160421 MGI 1615672 Acsm2 acyl-CoA synthetase medium-chain family member 2 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20220519 MGI 1615672 Acsm2 acyl-CoA synthetase medium-chain family member 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1615673 Plekha7 pleckstrin homology domain containing, family A member 7 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:26489655 1615673 Plekha7 pleckstrin homology domain containing, family A member 7 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:26489655 1615674 Tmem41b transmembrane protein 41B gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20220106 MGI PMID:34871328 1615674 Tmem41b transmembrane protein 41B gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:30352685 1615674 Tmem41b transmembrane protein 41B gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20220106 MGI PMID:34871328 1615674 Tmem41b transmembrane protein 41B gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20220106 MGI PMID:34871328 1615674 Tmem41b transmembrane protein 41B gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20220106 MGI PMID:34871328 1615674 Tmem41b transmembrane protein 41B gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:30352685 1615674 Tmem41b transmembrane protein 41B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615674 Tmem41b transmembrane protein 41B gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1615674 Tmem41b transmembrane protein 41B gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1615674 Tmem41b transmembrane protein 41B gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20200310 MGI PMID:30352685 1615674 Tmem41b transmembrane protein 41B gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20220106 MGI PMID:34871328 1615674 Tmem41b transmembrane protein 41B gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20220106 MGI PMID:34871328 1615676 Gprc5a G protein-coupled receptor, family C, group 5, member A gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:18000218 1615676 Gprc5a G protein-coupled receptor, family C, group 5, member A gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18000218 1615676 Gprc5a G protein-coupled receptor, family C, group 5, member A gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:18000218 1615676 Gprc5a G protein-coupled receptor, family C, group 5, member A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15677768 1615676 Gprc5a G protein-coupled receptor, family C, group 5, member A gene MP:0002871 albuminuria IAGP N RGD:5509061 20200917 MGI PMID:29636387 1615676 Gprc5a G protein-coupled receptor, family C, group 5, member A gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20200917 MGI PMID:29636387 1615676 Gprc5a G protein-coupled receptor, family C, group 5, member A gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:18000218 1615676 Gprc5a G protein-coupled receptor, family C, group 5, member A gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20200917 MGI PMID:29636387 1615676 Gprc5a G protein-coupled receptor, family C, group 5, member A gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20200917 MGI PMID:29636387 1615676 Gprc5a G protein-coupled receptor, family C, group 5, member A gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20200917 MGI PMID:29636387 1615680 Clec12a C-type lectin domain family 12, member a gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20151119 MGI PMID:24631154 1615680 Clec12a C-type lectin domain family 12, member a gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20160714 MGI PMID:26095365 1615680 Clec12a C-type lectin domain family 12, member a gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20151119 MGI PMID:24631154 1615680 Clec12a C-type lectin domain family 12, member a gene MP:0003674 oxidative stress IAGP N RGD:5509061 20151119 MGI PMID:24631154 1615680 Clec12a C-type lectin domain family 12, member a gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20160714 MGI PMID:26095365 1615680 Clec12a C-type lectin domain family 12, member a gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20151119 MGI PMID:24631154 1615680 Clec12a C-type lectin domain family 12, member a gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20151119 MGI PMID:24631154 1615680 Clec12a C-type lectin domain family 12, member a gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20151119 MGI PMID:24631154 1615680 Clec12a C-type lectin domain family 12, member a gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20160714 MGI PMID:26095365 1615683 Cytl1 cytokine-like 1 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:21652695 1615685 Dok7 docking protein 7 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1615685 Dok7 docking protein 7 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20150611 MGI PMID:25237101 1615685 Dok7 docking protein 7 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:16794080 1615685 Dok7 docking protein 7 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:16794080 1615685 Dok7 docking protein 7 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20150611 MGI PMID:25237101 1615685 Dok7 docking protein 7 gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1615685 Dok7 docking protein 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150611 MGI PMID:25237101 1615685 Dok7 docking protein 7 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20150611 MGI PMID:25237101 1615685 Dok7 docking protein 7 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20150611 MGI PMID:25237101 1615685 Dok7 docking protein 7 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:16794080 1615685 Dok7 docking protein 7 gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:16794080 1615685 Dok7 docking protein 7 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1615685 Dok7 docking protein 7 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1615685 Dok7 docking protein 7 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16794080 1615685 Dok7 docking protein 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615690 Ebf4 early B cell factor 4 gene MP:0001257 increased body length IEA N RGD:5509061 20220811 MGI 1615692 Bahd1 bromo adjacent homology domain containing 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1615692 Bahd1 bromo adjacent homology domain containing 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20181227 MGI 1615692 Bahd1 bromo adjacent homology domain containing 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20201022 MGI 1615692 Bahd1 bromo adjacent homology domain containing 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20181227 MGI 1615692 Bahd1 bromo adjacent homology domain containing 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21252314 1615692 Bahd1 bromo adjacent homology domain containing 1 gene MP:0005015 increased T cell number IEA N RGD:5509061 20211021 MGI 1615692 Bahd1 bromo adjacent homology domain containing 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 1615692 Bahd1 bromo adjacent homology domain containing 1 gene MP:0008039 increased NK T cell number IEA N RGD:5509061 20211021 MGI 1615692 Bahd1 bromo adjacent homology domain containing 1 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20211021 MGI 1615692 Bahd1 bromo adjacent homology domain containing 1 gene MP:0010851 decreased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20211021 MGI 1615692 Bahd1 bromo adjacent homology domain containing 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20181227 MGI 1615692 Bahd1 bromo adjacent homology domain containing 1 gene MP:0013511 increased CD4-negative NK T cell number IEA N RGD:5509061 20210128 MGI 1615692 Bahd1 bromo adjacent homology domain containing 1 gene MP:0013514 increased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20211021 MGI 1615695 Oosp3 oocyte secreted protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200723 MGI PMID:32231122 1615696 Oosp2 oocyte secreted protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200723 MGI PMID:32231122 1615697 Cyb561a3 cytochrome b561 family, member A3 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1615697 Cyb561a3 cytochrome b561 family, member A3 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20200310 MGI 1615697 Cyb561a3 cytochrome b561 family, member A3 gene MP:0001304 cataract IEA N RGD:5509061 20200310 MGI 1615697 Cyb561a3 cytochrome b561 family, member A3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1615697 Cyb561a3 cytochrome b561 family, member A3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20200310 MGI 1615698 Myrf myelin regulatory factor gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19596243 1615698 Myrf myelin regulatory factor gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:19596243 1615698 Myrf myelin regulatory factor gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19596243 1615698 Myrf myelin regulatory factor gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:19596243 1615698 Myrf myelin regulatory factor gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200116 MGI PMID:31048900 1615698 Myrf myelin regulatory factor gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19596243 1615698 Myrf myelin regulatory factor gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19596243 1615698 Myrf myelin regulatory factor gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 1615698 Myrf myelin regulatory factor gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20230601 MGI 1615698 Myrf myelin regulatory factor gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:19596243 1615698 Myrf myelin regulatory factor gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1615698 Myrf myelin regulatory factor gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200116 MGI PMID:31048900 1615698 Myrf myelin regulatory factor gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200116 MGI PMID:31048900 1615698 Myrf myelin regulatory factor gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20200116 MGI PMID:31048900 1615698 Myrf myelin regulatory factor gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20200116 MGI PMID:31048900 1615698 Myrf myelin regulatory factor gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20200116 MGI PMID:31048900 1615698 Myrf myelin regulatory factor gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:31048900 1615698 Myrf myelin regulatory factor gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20200116 MGI PMID:31048900 1615698 Myrf myelin regulatory factor gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200116 MGI PMID:31048900 1615698 Myrf myelin regulatory factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19596243 1615698 Myrf myelin regulatory factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1615698 Myrf myelin regulatory factor gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20240627 MGI 1615698 Myrf myelin regulatory factor gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200116 MGI PMID:31048900 1615698 Myrf myelin regulatory factor gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20230601 MGI 1615700 Rab40c Rab40C, member RAS oncogene family gene MP:0002080 prenatal lethality IEA N RGD:5509061 20201231 MGI 1615700 Rab40c Rab40C, member RAS oncogene family gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1615700 Rab40c Rab40C, member RAS oncogene family gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160421 MGI 1615700 Rab40c Rab40C, member RAS oncogene family gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1615702 Phactr1 phosphatase and actin regulator 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20201022 MGI 1615702 Phactr1 phosphatase and actin regulator 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20201022 MGI 1615702 Phactr1 phosphatase and actin regulator 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1615702 Phactr1 phosphatase and actin regulator 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1615702 Phactr1 phosphatase and actin regulator 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1615702 Phactr1 phosphatase and actin regulator 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1615702 Phactr1 phosphatase and actin regulator 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220519 MGI 1615702 Phactr1 phosphatase and actin regulator 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 1615702 Phactr1 phosphatase and actin regulator 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1615702 Phactr1 phosphatase and actin regulator 1 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20240912 MGI PMID:35653516 1615702 Phactr1 phosphatase and actin regulator 1 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20201022 MGI 1615702 Phactr1 phosphatase and actin regulator 1 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20220519 MGI 1615702 Phactr1 phosphatase and actin regulator 1 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20201022 MGI 1615702 Phactr1 phosphatase and actin regulator 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20181227 MGI 1615703 Sycp2l synaptonemal complex protein 2-like gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20151112 MGI PMID:26362258 1615703 Sycp2l synaptonemal complex protein 2-like gene MP:0001935 decreased litter size IAGP N RGD:5509061 20151112 MGI PMID:26362258 1615703 Sycp2l synaptonemal complex protein 2-like gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20151112 MGI PMID:26362258 1615703 Sycp2l synaptonemal complex protein 2-like gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20160428 MGI PMID:26362258 1615703 Sycp2l synaptonemal complex protein 2-like gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20151112 MGI PMID:26362258 1615703 Sycp2l synaptonemal complex protein 2-like gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20151112 MGI PMID:26362258 1615703 Sycp2l synaptonemal complex protein 2-like gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:26362258 1615704 Ofcc1 orofacial cleft 1 candidate 1 gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20240523 MGI 1615704 Ofcc1 orofacial cleft 1 candidate 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1615704 Ofcc1 orofacial cleft 1 candidate 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20230601 MGI 1615704 Ofcc1 orofacial cleft 1 candidate 1 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20151112 MGI PMID:22242126 1615704 Ofcc1 orofacial cleft 1 candidate 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20201022 MGI 1615704 Ofcc1 orofacial cleft 1 candidate 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1615704 Ofcc1 orofacial cleft 1 candidate 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20141003 MGI 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20141003 MGI 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20151126 MGI PMID:22723910 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22406534 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22664872 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20151126 MGI PMID:22723910 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20151126 MGI PMID:22723910 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20151126 MGI PMID:22723910 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20151126 MGI PMID:22723910 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151126 MGI PMID:22723910 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001297 microphthalmia IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20151126 MGI PMID:22723910 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001304 cataract IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001306 small lens IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001314 cornea opacity IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001317 abnormal pupil morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:22664872 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001349 excessive tearing IEA N RGD:5509061 20141003 MGI 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001512 trunk curl IEA N RGD:5509061 20170105 MGI 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:22664872 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22664872 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20141003 MGI 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22406534 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22406534 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22406534 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0002697 abnormal eye size IEA N RGD:5509061 20141003 MGI 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0003671 abnormal eyelid aperture IEA N RGD:5509061 20141003 MGI 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0004149 increased bone strength IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20141003 MGI 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22406534 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22664872 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20151126 MGI PMID:22723910 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22664872 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22406534 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22664872 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22406534 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22664872 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22406534 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22664872 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22406534 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22664872 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22406534 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20151126 MGI PMID:22723910 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:22406534 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:22664872 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22406534 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22406534 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22664872 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20151126 MGI PMID:22723910 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0009859 eye opacity IAGP N RGD:5509061 20141003 MGI PMID:22664872 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0009859 eye opacity IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22406534 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20141003 MGI 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20160922 MGI PMID:24652767 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200402 MGI 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0013393 symblepharon IAGP N RGD:5509061 20141218 MGI PMID:22406534 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0013701 abnormal mature B cell number IAGP N RGD:5509061 20151126 MGI PMID:22723910 1615706 Spns2 SPNS lysolipid transporter 2, sphingosine-1-phosphate gene MP:0020117 decreased sphingosine level IAGP N RGD:5509061 20151126 MGI PMID:22723910 1615709 Mgl2 macrophage galactose N-acetyl-galactosamine specific lectin 2 gene MP:0000701 abnormal lymph node size IAGP N RGD:5509061 20141003 MGI PMID:24076051 1615709 Mgl2 macrophage galactose N-acetyl-galactosamine specific lectin 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:24076051 1615709 Mgl2 macrophage galactose N-acetyl-galactosamine specific lectin 2 gene MP:0002434 abnormal T-helper 2 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24076051 1615709 Mgl2 macrophage galactose N-acetyl-galactosamine specific lectin 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:24076051 1615709 Mgl2 macrophage galactose N-acetyl-galactosamine specific lectin 2 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:24076051 1615709 Mgl2 macrophage galactose N-acetyl-galactosamine specific lectin 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24076051 1615709 Mgl2 macrophage galactose N-acetyl-galactosamine specific lectin 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24076051 1615709 Mgl2 macrophage galactose N-acetyl-galactosamine specific lectin 2 gene MP:0008119 decreased Langerhans cell number IAGP N RGD:5509061 20141003 MGI PMID:24076051 1615709 Mgl2 macrophage galactose N-acetyl-galactosamine specific lectin 2 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:24076051 1615709 Mgl2 macrophage galactose N-acetyl-galactosamine specific lectin 2 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:24076051 1615711 Flcn folliculin gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18974783 1615711 Flcn folliculin gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:21258407 1615711 Flcn folliculin gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22709692 1615711 Flcn folliculin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20170525 MGI PMID:25775561 1615711 Flcn folliculin gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:21258407 1615711 Flcn folliculin gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:18974783 1615711 Flcn folliculin gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:22709692 1615711 Flcn folliculin gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:19234517 1615711 Flcn folliculin gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:22709692 1615711 Flcn folliculin gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:18974783 1615711 Flcn folliculin gene MP:0004192 abnormal kidney pyramid morphology IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:19234517 1615711 Flcn folliculin gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:18974783 1615711 Flcn folliculin gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22709692 1615711 Flcn folliculin gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18974783 1615711 Flcn folliculin gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:18974783 1615711 Flcn folliculin gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20170525 MGI PMID:25775561 1615711 Flcn folliculin gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:18974783 1615711 Flcn folliculin gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18974783 1615711 Flcn folliculin gene MP:0010294 increased kidney tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19234517 1615711 Flcn folliculin gene MP:0010384 increased renal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18974783 1615711 Flcn folliculin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18974783 1615711 Flcn folliculin gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19234517 1615711 Flcn folliculin gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18974783 1615711 Flcn folliculin gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21258407 1615711 Flcn folliculin gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20141003 MGI PMID:18974783 1615711 Flcn folliculin gene MP:0011376 abnormal kidney corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18182616 1615711 Flcn folliculin gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19234517 1615712 Fam117a family with sequence similarity 117, member A gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220519 MGI 1615713 Syna syncytin a gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:19564597 1615713 Syna syncytin a gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:22032925 1615713 Syna syncytin a gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19564597 1615713 Syna syncytin a gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:19564597 1615713 Syna syncytin a gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19564597 1615713 Syna syncytin a gene MP:0004265 abnormal placental transport IAGP N RGD:5509061 20141003 MGI PMID:19564597 1615713 Syna syncytin a gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:19564597 1615713 Syna syncytin a gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:19564597 1615713 Syna syncytin a gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19564597 1615713 Syna syncytin a gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22032925 1615713 Syna syncytin a gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22032925 1615713 Syna syncytin a gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22032925 1615714 Tut7 terminal uridylyl transferase 7 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20181227 MGI PMID:28792939 1615714 Tut7 terminal uridylyl transferase 7 gene MP:0001926 female infertility IAGP N RGD:5509061 20181227 MGI PMID:28792939 1615714 Tut7 terminal uridylyl transferase 7 gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20181227 MGI PMID:28792939 1615714 Tut7 terminal uridylyl transferase 7 gene MP:0014445 abnormal spindle assembly in female meiosis IAGP N RGD:5509061 20240509 MGI PMID:28792939 1615715 Ccdc9b coiled-coil domain containing 9B gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1615715 Ccdc9b coiled-coil domain containing 9B gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1615717 Scfd2 Sec1 family domain containing 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1615717 Scfd2 Sec1 family domain containing 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230119 MGI 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0002946 delayed axon extension IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0003247 abnormal glutaminergic neuron morphology IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230601 MGI 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1615720 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 gene MP:0020069 decreased neocortex size IAGP N RGD:5509061 20171214 MGI PMID:28414797 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210520 MGI 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20201022 MGI 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20201022 MGI 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0002989 small kidney IEA N RGD:5509061 20201022 MGI 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20170928 MGI PMID:26656251 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20210520 MGI 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20170928 MGI PMID:26656251 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20170928 MGI PMID:26656251 1615721 Mgst2 microsomal glutathione S-transferase 2 gene MP:0031601 decreased endoplasmic reticulum stress IAGP N RGD:5509061 20240418 MGI PMID:26656251 1615722 Cspp1 centrosome and spindle pole associated protein 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1615722 Cspp1 centrosome and spindle pole associated protein 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1615722 Cspp1 centrosome and spindle pole associated protein 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1615722 Cspp1 centrosome and spindle pole associated protein 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1615722 Cspp1 centrosome and spindle pole associated protein 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0000746 weakness IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001127 small ovary IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12893777 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001147 small testis IAGP N RGD:5509061 20160609 MGI PMID:26637282 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12893777 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:12893777 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001577 anemia IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12893777 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12893777 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12893777 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20160609 MGI PMID:26637282 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20211216 MGI PMID:31219578 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12893777 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0003078 aphakia IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20211216 MGI PMID:31219578 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12893777 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20170608 MGI PMID:26980189 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20211216 MGI PMID:31219578 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12893777 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12893777 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20230119 MGI 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:12893777 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20170601 MGI PMID:26980188 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20170608 MGI PMID:26980189 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230119 MGI 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12893777 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20150122 MGI PMID:22922648 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12893777 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18180189 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19217432 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20211216 MGI PMID:31219578 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20200310 MGI PMID:31078270 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21734703 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0014040 increased cellular sensitivity to DNA damaging agents IAGP N RGD:5509061 20160609 MGI PMID:26637282 1615723 Fancd2 Fanconi anemia, complementation group D2 gene MP:0014040 increased cellular sensitivity to DNA damaging agents IAGP N RGD:5509061 20211216 MGI PMID:31219578 1615724 Plac9 placenta specific 9 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20231207 MGI 1615724 Plac9 placenta specific 9 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1615724 Plac9 placenta specific 9 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20231207 MGI 1615724 Plac9 placenta specific 9 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20231207 MGI 1615724 Plac9 placenta specific 9 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1615724 Plac9 placenta specific 9 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20231207 MGI 1615724 Plac9 placenta specific 9 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 1615724 Plac9 placenta specific 9 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20231207 MGI 1615725 Ptchd1 patched domain containing 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1615725 Ptchd1 patched domain containing 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20170105 MGI 1615725 Ptchd1 patched domain containing 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 1615725 Ptchd1 patched domain containing 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160929 MGI PMID:27007844 1615725 Ptchd1 patched domain containing 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160929 MGI PMID:27007844 1615725 Ptchd1 patched domain containing 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1615725 Ptchd1 patched domain containing 1 gene MP:0001454 abnormal cued conditioning behavior IEA N RGD:5509061 20211021 MGI 1615725 Ptchd1 patched domain containing 1 gene MP:0001469 abnormal contextual conditioning behavior IEA N RGD:5509061 20210128 MGI 1615725 Ptchd1 patched domain containing 1 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20160929 MGI PMID:27007844 1615725 Ptchd1 patched domain containing 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20170105 MGI 1615725 Ptchd1 patched domain containing 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1615725 Ptchd1 patched domain containing 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220519 MGI 1615725 Ptchd1 patched domain containing 1 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20160929 MGI PMID:27007844 1615725 Ptchd1 patched domain containing 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 1615725 Ptchd1 patched domain containing 1 gene MP:0004144 hypotonia IAGP N RGD:5509061 20160929 MGI PMID:27007844 1615725 Ptchd1 patched domain containing 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1615725 Ptchd1 patched domain containing 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1615725 Ptchd1 patched domain containing 1 gene MP:0005655 increased aggression IAGP N RGD:5509061 20160929 MGI PMID:27007844 1615725 Ptchd1 patched domain containing 1 gene MP:0009436 fragmentation of sleep/wake states IAGP N RGD:5509061 20220922 MGI PMID:27007844 1615725 Ptchd1 patched domain containing 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20160929 MGI PMID:27007844 1615725 Ptchd1 patched domain containing 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20160929 MGI PMID:27007844 1615725 Ptchd1 patched domain containing 1 gene MP:0012312 impaired avoidance learning behavior IAGP N RGD:5509061 20160929 MGI PMID:27007844 1615725 Ptchd1 patched domain containing 1 gene MP:0014114 abnormal cognition IAGP N RGD:5509061 20160929 MGI PMID:27007844 1615728 Tns2 tensin 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:2806394 1615728 Tns2 tensin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:2806394 1615728 Tns2 tensin 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:2806394 1615728 Tns2 tensin 2 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16688531 1615728 Tns2 tensin 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:16688531 1615728 Tns2 tensin 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:2523501 1615728 Tns2 tensin 2 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:2523501 1615730 C2cd2 C2 calcium-dependent domain containing 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1615733 Gtpbp10 GTP-binding protein 10 (putative) gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1615733 Gtpbp10 GTP-binding protein 10 (putative) gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210128 MGI 1615733 Gtpbp10 GTP-binding protein 10 (putative) gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20240523 MGI 1615733 Gtpbp10 GTP-binding protein 10 (putative) gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1615733 Gtpbp10 GTP-binding protein 10 (putative) gene MP:0002626 increased heart rate IEA N RGD:5509061 20201022 MGI 1615733 Gtpbp10 GTP-binding protein 10 (putative) gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230601 MGI 1615733 Gtpbp10 GTP-binding protein 10 (putative) gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20220811 MGI 1615733 Gtpbp10 GTP-binding protein 10 (putative) gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1615733 Gtpbp10 GTP-binding protein 10 (putative) gene MP:0010052 increased grip strength IEA N RGD:5509061 20220519 MGI 1615733 Gtpbp10 GTP-binding protein 10 (putative) gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220519 MGI 1615733 Gtpbp10 GTP-binding protein 10 (putative) gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1615739 Rspo1 R-spondin 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170105 MGI 1615739 Rspo1 R-spondin 1 gene MP:0001147 small testis IEA N RGD:5509061 20170105 MGI 1615739 Rspo1 R-spondin 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:18250097 1615739 Rspo1 R-spondin 1 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1615739 Rspo1 R-spondin 1 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:24036309 1615739 Rspo1 R-spondin 1 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20201022 MGI 1615739 Rspo1 R-spondin 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170105 MGI 1615739 Rspo1 R-spondin 1 gene MP:0002175 decreased brain weight IEA N RGD:5509061 20211021 MGI 1615739 Rspo1 R-spondin 1 gene MP:0002208 abnormal germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24036309 1615739 Rspo1 R-spondin 1 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:18250097 1615739 Rspo1 R-spondin 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20181227 MGI 1615739 Rspo1 R-spondin 1 gene MP:0002783 abnormal ovary secretion IAGP N RGD:5509061 20141003 MGI PMID:18250097 1615739 Rspo1 R-spondin 1 gene MP:0002787 pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:18250097 1615739 Rspo1 R-spondin 1 gene MP:0002787 pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:18250098 1615739 Rspo1 R-spondin 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1615739 Rspo1 R-spondin 1 gene MP:0003582 abnormal ovary development IAGP N RGD:5509061 20141003 MGI PMID:18250097 1615739 Rspo1 R-spondin 1 gene MP:0003582 abnormal ovary development IAGP N RGD:5509061 20141003 MGI PMID:18250098 1615739 Rspo1 R-spondin 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20181227 MGI 1615739 Rspo1 R-spondin 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160114 MGI 1615739 Rspo1 R-spondin 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1615739 Rspo1 R-spondin 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1615739 Rspo1 R-spondin 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:18250098 1615739 Rspo1 R-spondin 1 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:18250097 1615739 Rspo1 R-spondin 1 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:24036309 1615739 Rspo1 R-spondin 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1615739 Rspo1 R-spondin 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160114 MGI 1615739 Rspo1 R-spondin 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1615739 Rspo1 R-spondin 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 1615739 Rspo1 R-spondin 1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18250098 1615739 Rspo1 R-spondin 1 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:24036309 1615739 Rspo1 R-spondin 1 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20181227 MGI 1615739 Rspo1 R-spondin 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20181227 MGI 1615740 Lrrc4 leucine rich repeat containing 4 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17973922 1615740 Lrrc4 leucine rich repeat containing 4 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17973922 1615740 Lrrc4 leucine rich repeat containing 4 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:17973922 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0002188 small heart IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0003794 delayed somite formation IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0004259 small placenta IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0004560 abnormal chorionic plate morphology IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0009489 abnormal blood vessel endothelium morphology IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615741 Bcas3 BCAS3 microtubule associated cell migration factor gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20180913 MGI PMID:29618843 1615743 Stab2 stabilin 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:21293057 1615743 Stab2 stabilin 2 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22371575 1615743 Stab2 stabilin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21293057 1615743 Stab2 stabilin 2 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:21293057 1615743 Stab2 stabilin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21293057 1615743 Stab2 stabilin 2 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:21293057 1615743 Stab2 stabilin 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:21293057 1615743 Stab2 stabilin 2 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21293057 1615743 Stab2 stabilin 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:21293057 1615743 Stab2 stabilin 2 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:21293057 1615743 Stab2 stabilin 2 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22371575 1615743 Stab2 stabilin 2 gene MP:0011009 increased circulating glutamate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:21293057 1615743 Stab2 stabilin 2 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21293057 1615743 Stab2 stabilin 2 gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21293057 1615743 Stab2 stabilin 2 gene MP:0014427 increased circulating hyaluronic acid level IAGP N RGD:5509061 20240425 MGI PMID:22371575 1615744 Nadk NAD kinase gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1615744 Nadk NAD kinase gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1615744 Nadk NAD kinase gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20190502 MGI 1615744 Nadk NAD kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615744 Nadk NAD kinase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1615746 Eif4a3 eukaryotic translation initiation factor 4A3 gene MP:0000433 microcephaly IAGP N RGD:5509061 20200102 MGI PMID:27618312 1615746 Eif4a3 eukaryotic translation initiation factor 4A3 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200102 MGI PMID:27618312 1615746 Eif4a3 eukaryotic translation initiation factor 4A3 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20200102 MGI PMID:27618312 1615746 Eif4a3 eukaryotic translation initiation factor 4A3 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20200102 MGI PMID:27618312 1615746 Eif4a3 eukaryotic translation initiation factor 4A3 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20200102 MGI PMID:27618312 1615746 Eif4a3 eukaryotic translation initiation factor 4A3 gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20200102 MGI PMID:27618312 1615746 Eif4a3 eukaryotic translation initiation factor 4A3 gene MP:0012683 absent telencephalon IAGP N RGD:5509061 20200102 MGI PMID:27618312 1615746 Eif4a3 eukaryotic translation initiation factor 4A3 gene MP:0020069 decreased neocortex size IAGP N RGD:5509061 20200102 MGI PMID:27618312 1615748 Pcdha9 protocadherin alpha 9 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20170831 MGI PMID:28530678 1615748 Pcdha9 protocadherin alpha 9 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20170824 MGI PMID:28530678 1615748 Pcdha9 protocadherin alpha 9 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20170831 MGI PMID:28530678 1615748 Pcdha9 protocadherin alpha 9 gene MP:0010463 aorta stenosis IAGP N RGD:5509061 20170824 MGI PMID:28530678 1615748 Pcdha9 protocadherin alpha 9 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20170824 MGI PMID:28530678 1615748 Pcdha9 protocadherin alpha 9 gene MP:0010541 aorta hypoplasia IAGP N RGD:5509061 20170824 MGI PMID:28530678 1615748 Pcdha9 protocadherin alpha 9 gene MP:0010580 decreased heart left ventricle size IAGP N RGD:5509061 20170831 MGI PMID:28530678 1615748 Pcdha9 protocadherin alpha 9 gene MP:0031523 mitral valve hypoplasia IAGP N RGD:5509061 20240104 MGI PMID:28530678 1615749 Pkd1l1 polycystic kidney disease 1 like 1 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:21307093 1615749 Pkd1l1 polycystic kidney disease 1 like 1 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:21307093 1615749 Pkd1l1 polycystic kidney disease 1 like 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:21307093 1615749 Pkd1l1 polycystic kidney disease 1 like 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:21307093 1615749 Pkd1l1 polycystic kidney disease 1 like 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21307093 1615749 Pkd1l1 polycystic kidney disease 1 like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21307093 1615749 Pkd1l1 polycystic kidney disease 1 like 1 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:20080492 1615749 Pkd1l1 polycystic kidney disease 1 like 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21307093 1615749 Pkd1l1 polycystic kidney disease 1 like 1 gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:21307093 1615749 Pkd1l1 polycystic kidney disease 1 like 1 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:21307093 1615749 Pkd1l1 polycystic kidney disease 1 like 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20080492 1615749 Pkd1l1 polycystic kidney disease 1 like 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21307093 1615751 Pcdha1 protocadherin alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17572674 1615752 Foxp2 forkhead box P2 gene MP:0000054 delayed ear emergence IAGP N RGD:5509061 20141003 MGI PMID:15983371 1615752 Foxp2 forkhead box P2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17619227 1615752 Foxp2 forkhead box P2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:18328704 1615752 Foxp2 forkhead box P2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:18328704 1615752 Foxp2 forkhead box P2 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15983371 1615752 Foxp2 forkhead box P2 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:15983371 1615752 Foxp2 forkhead box P2 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:15983371 1615752 Foxp2 forkhead box P2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17428829 1615752 Foxp2 forkhead box P2 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:17428829 1615752 Foxp2 forkhead box P2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17619227 1615752 Foxp2 forkhead box P2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:15983371 1615752 Foxp2 forkhead box P2 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:17619227 1615752 Foxp2 forkhead box P2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15983371 1615752 Foxp2 forkhead box P2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:18328704 1615752 Foxp2 forkhead box P2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:15983371 1615752 Foxp2 forkhead box P2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:17619227 1615752 Foxp2 forkhead box P2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:18328704 1615752 Foxp2 forkhead box P2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17428829 1615752 Foxp2 forkhead box P2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15983371 1615752 Foxp2 forkhead box P2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:15983371 1615752 Foxp2 forkhead box P2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18328704 1615752 Foxp2 forkhead box P2 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:18328704 1615752 Foxp2 forkhead box P2 gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20141003 MGI PMID:18328704 1615752 Foxp2 forkhead box P2 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:18328704 1615752 Foxp2 forkhead box P2 gene MP:0003159 abnormal esophageal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17428829 1615752 Foxp2 forkhead box P2 gene MP:0003160 abnormal esophagus development IAGP N RGD:5509061 20141003 MGI PMID:17428829 1615752 Foxp2 forkhead box P2 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:17428829 1615752 Foxp2 forkhead box P2 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15983371 1615752 Foxp2 forkhead box P2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0004391 abnormal respiratory conducting tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17428829 1615752 Foxp2 forkhead box P2 gene MP:0004548 dilated esophagus IAGP N RGD:5509061 20141003 MGI PMID:17428829 1615752 Foxp2 forkhead box P2 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0005356 positive geotaxis IAGP N RGD:5509061 20141003 MGI PMID:15983371 1615752 Foxp2 forkhead box P2 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:17428829 1615752 Foxp2 forkhead box P2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:17428829 1615752 Foxp2 forkhead box P2 gene MP:0006357 abnormal circulating mineral level IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18328704 1615752 Foxp2 forkhead box P2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:15983371 1615752 Foxp2 forkhead box P2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:17619227 1615752 Foxp2 forkhead box P2 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20180301 MGI PMID:18328704 1615752 Foxp2 forkhead box P2 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0010394 decreased QRS amplitude IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:17428829 1615752 Foxp2 forkhead box P2 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17428829 1615752 Foxp2 forkhead box P2 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17619227 1615752 Foxp2 forkhead box P2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15983371 1615752 Foxp2 forkhead box P2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17428829 1615752 Foxp2 forkhead box P2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17428829 1615752 Foxp2 forkhead box P2 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0011148 decreased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:17428829 1615752 Foxp2 forkhead box P2 gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20141003 MGI PMID:19490899 1615752 Foxp2 forkhead box P2 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:15983371 1615752 Foxp2 forkhead box P2 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:18287060 1615752 Foxp2 forkhead box P2 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:19490899 1615753 Igh immunoglobulin heavy chain complex gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16204304 1615753 Igh immunoglobulin heavy chain complex gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:16456003 1615753 Igh immunoglobulin heavy chain complex gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:9430222 1615753 Igh immunoglobulin heavy chain complex gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20210520 MGI PMID:30289441 1615753 Igh immunoglobulin heavy chain complex gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:19573810 1615753 Igh immunoglobulin heavy chain complex gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15735016 1615753 Igh immunoglobulin heavy chain complex gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:14707052 1615753 Igh immunoglobulin heavy chain complex gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:15699070 1615753 Igh immunoglobulin heavy chain complex gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15735016 1615753 Igh immunoglobulin heavy chain complex gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19332766 1615753 Igh immunoglobulin heavy chain complex gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19573810 1615753 Igh immunoglobulin heavy chain complex gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:15879114 1615753 Igh immunoglobulin heavy chain complex gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17082616 1615753 Igh immunoglobulin heavy chain complex gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15735016 1615753 Igh immunoglobulin heavy chain complex gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19573810 1615753 Igh immunoglobulin heavy chain complex gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:9794392 1615753 Igh immunoglobulin heavy chain complex gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:16754718 1615753 Igh immunoglobulin heavy chain complex gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12471120 1615753 Igh immunoglobulin heavy chain complex gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15699070 1615753 Igh immunoglobulin heavy chain complex gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:14962903 1615753 Igh immunoglobulin heavy chain complex gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16754718 1615753 Igh immunoglobulin heavy chain complex gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12471120 1615753 Igh immunoglobulin heavy chain complex gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15879114 1615753 Igh immunoglobulin heavy chain complex gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16272317 1615753 Igh immunoglobulin heavy chain complex gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16754718 1615753 Igh immunoglobulin heavy chain complex gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:19615922 1615753 Igh immunoglobulin heavy chain complex gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23940273 1615753 Igh immunoglobulin heavy chain complex gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12471120 1615753 Igh immunoglobulin heavy chain complex gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:22250990 1615753 Igh immunoglobulin heavy chain complex gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20230309 MGI PMID:29907762 1615753 Igh immunoglobulin heavy chain complex gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20150129 MGI PMID:24706858 1615753 Igh immunoglobulin heavy chain complex gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210520 MGI PMID:30289441 1615753 Igh immunoglobulin heavy chain complex gene MP:0001935 decreased litter size IAGP N RGD:5509061 20210520 MGI PMID:30289441 1615753 Igh immunoglobulin heavy chain complex gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15735016 1615753 Igh immunoglobulin heavy chain complex gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20393505 1615753 Igh immunoglobulin heavy chain complex gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15735016 1615753 Igh immunoglobulin heavy chain complex gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19573810 1615753 Igh immunoglobulin heavy chain complex gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20393505 1615753 Igh immunoglobulin heavy chain complex gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:19332766 1615753 Igh immunoglobulin heavy chain complex gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19573810 1615753 Igh immunoglobulin heavy chain complex gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10449518 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11160315 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12119344 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12354384 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15699070 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16204304 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16456003 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16860756 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17082616 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18056289 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20036775 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21909113 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9075923 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9390689 1615753 Igh immunoglobulin heavy chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9430222 1615753 Igh immunoglobulin heavy chain complex gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12471120 1615753 Igh immunoglobulin heavy chain complex gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:14707052 1615753 Igh immunoglobulin heavy chain complex gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:14707052 1615753 Igh immunoglobulin heavy chain complex gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:10449518 1615753 Igh immunoglobulin heavy chain complex gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10639146 1615753 Igh immunoglobulin heavy chain complex gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11896394 1615753 Igh immunoglobulin heavy chain complex gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17185562 1615753 Igh immunoglobulin heavy chain complex gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18322191 1615753 Igh immunoglobulin heavy chain complex gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19070574 1615753 Igh immunoglobulin heavy chain complex gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19615922 1615753 Igh immunoglobulin heavy chain complex gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12471120 1615753 Igh immunoglobulin heavy chain complex gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15699070 1615753 Igh immunoglobulin heavy chain complex gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16272317 1615753 Igh immunoglobulin heavy chain complex gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12668643 1615753 Igh immunoglobulin heavy chain complex gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15699070 1615753 Igh immunoglobulin heavy chain complex gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:22051050 1615753 Igh immunoglobulin heavy chain complex gene MP:0002491 decreased IgD level IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12471120 1615753 Igh immunoglobulin heavy chain complex gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20230309 MGI PMID:29907762 1615753 Igh immunoglobulin heavy chain complex gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11896394 1615753 Igh immunoglobulin heavy chain complex gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11896394 1615753 Igh immunoglobulin heavy chain complex gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12668643 1615753 Igh immunoglobulin heavy chain complex gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22250990 1615753 Igh immunoglobulin heavy chain complex gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12668643 1615753 Igh immunoglobulin heavy chain complex gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15699070 1615753 Igh immunoglobulin heavy chain complex gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15879114 1615753 Igh immunoglobulin heavy chain complex gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:20511552 1615753 Igh immunoglobulin heavy chain complex gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:24019479 1615753 Igh immunoglobulin heavy chain complex gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:14707052 1615753 Igh immunoglobulin heavy chain complex gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16973388 1615753 Igh immunoglobulin heavy chain complex gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:15879114 1615753 Igh immunoglobulin heavy chain complex gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:11896394 1615753 Igh immunoglobulin heavy chain complex gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12119344 1615753 Igh immunoglobulin heavy chain complex gene MP:0003133 increased early pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16754718 1615753 Igh immunoglobulin heavy chain complex gene MP:0003133 increased early pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0003134 increased late pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16272317 1615753 Igh immunoglobulin heavy chain complex gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:20393505 1615753 Igh immunoglobulin heavy chain complex gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:16888003 1615753 Igh immunoglobulin heavy chain complex gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:17713479 1615753 Igh immunoglobulin heavy chain complex gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:19070574 1615753 Igh immunoglobulin heavy chain complex gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:19070574 1615753 Igh immunoglobulin heavy chain complex gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17713479 1615753 Igh immunoglobulin heavy chain complex gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:11114372 1615753 Igh immunoglobulin heavy chain complex gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:20511552 1615753 Igh immunoglobulin heavy chain complex gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:9697840 1615753 Igh immunoglobulin heavy chain complex gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20210513 MGI PMID:33526923 1615753 Igh immunoglobulin heavy chain complex gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:17713479 1615753 Igh immunoglobulin heavy chain complex gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:19450527 1615753 Igh immunoglobulin heavy chain complex gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:20368578 1615753 Igh immunoglobulin heavy chain complex gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:20511552 1615753 Igh immunoglobulin heavy chain complex gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22250990 1615753 Igh immunoglobulin heavy chain complex gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:24019479 1615753 Igh immunoglobulin heavy chain complex gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20230309 MGI PMID:29907762 1615753 Igh immunoglobulin heavy chain complex gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12668643 1615753 Igh immunoglobulin heavy chain complex gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14707052 1615753 Igh immunoglobulin heavy chain complex gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19114667 1615753 Igh immunoglobulin heavy chain complex gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19332766 1615753 Igh immunoglobulin heavy chain complex gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0004940 abnormal B-1 B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10449518 1615753 Igh immunoglobulin heavy chain complex gene MP:0004940 abnormal B-1 B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16791880 1615753 Igh immunoglobulin heavy chain complex gene MP:0004942 abnormal B cell selection IAGP N RGD:5509061 20141003 MGI PMID:18322191 1615753 Igh immunoglobulin heavy chain complex gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22709692 1615753 Igh immunoglobulin heavy chain complex gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10449518 1615753 Igh immunoglobulin heavy chain complex gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19332766 1615753 Igh immunoglobulin heavy chain complex gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19879843 1615753 Igh immunoglobulin heavy chain complex gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23940273 1615753 Igh immunoglobulin heavy chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12119344 1615753 Igh immunoglobulin heavy chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15699070 1615753 Igh immunoglobulin heavy chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16204304 1615753 Igh immunoglobulin heavy chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16754718 1615753 Igh immunoglobulin heavy chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16860756 1615753 Igh immunoglobulin heavy chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19114667 1615753 Igh immunoglobulin heavy chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19615922 1615753 Igh immunoglobulin heavy chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20036775 1615753 Igh immunoglobulin heavy chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9323135 1615753 Igh immunoglobulin heavy chain complex gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0005022 abnormal immature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19114667 1615753 Igh immunoglobulin heavy chain complex gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19615922 1615753 Igh immunoglobulin heavy chain complex gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11896394 1615753 Igh immunoglobulin heavy chain complex gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15735016 1615753 Igh immunoglobulin heavy chain complex gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16973388 1615753 Igh immunoglobulin heavy chain complex gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:12471120 1615753 Igh immunoglobulin heavy chain complex gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:22709692 1615753 Igh immunoglobulin heavy chain complex gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:19615922 1615753 Igh immunoglobulin heavy chain complex gene MP:0008100 absent plasma cells IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19332766 1615753 Igh immunoglobulin heavy chain complex gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:16973388 1615753 Igh immunoglobulin heavy chain complex gene MP:0008164 abnormal B-1a B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19114667 1615753 Igh immunoglobulin heavy chain complex gene MP:0008166 abnormal B-2 B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12668643 1615753 Igh immunoglobulin heavy chain complex gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:16754718 1615753 Igh immunoglobulin heavy chain complex gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0008169 increased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0008170 decreased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:16754718 1615753 Igh immunoglobulin heavy chain complex gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19114667 1615753 Igh immunoglobulin heavy chain complex gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:12668643 1615753 Igh immunoglobulin heavy chain complex gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:15699070 1615753 Igh immunoglobulin heavy chain complex gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:16754718 1615753 Igh immunoglobulin heavy chain complex gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:9323135 1615753 Igh immunoglobulin heavy chain complex gene MP:0008175 absent follicular B cells IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0008180 abnormal marginal zone B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:15699070 1615753 Igh immunoglobulin heavy chain complex gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16754718 1615753 Igh immunoglobulin heavy chain complex gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12668643 1615753 Igh immunoglobulin heavy chain complex gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:14707052 1615753 Igh immunoglobulin heavy chain complex gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:9323135 1615753 Igh immunoglobulin heavy chain complex gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:19879843 1615753 Igh immunoglobulin heavy chain complex gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16860756 1615753 Igh immunoglobulin heavy chain complex gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20036775 1615753 Igh immunoglobulin heavy chain complex gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:12119344 1615753 Igh immunoglobulin heavy chain complex gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:16754718 1615753 Igh immunoglobulin heavy chain complex gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0008202 absent B-1 B cells IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0008203 absent B-1a cells IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0008204 absent B-1b cells IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0008205 absent B-2 B cells IAGP N RGD:5509061 20141003 MGI PMID:22709692 1615753 Igh immunoglobulin heavy chain complex gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16272317 1615753 Igh immunoglobulin heavy chain complex gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16754718 1615753 Igh immunoglobulin heavy chain complex gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20036775 1615753 Igh immunoglobulin heavy chain complex gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21909113 1615753 Igh immunoglobulin heavy chain complex gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16860756 1615753 Igh immunoglobulin heavy chain complex gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17082616 1615753 Igh immunoglobulin heavy chain complex gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18322191 1615753 Igh immunoglobulin heavy chain complex gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:19879843 1615753 Igh immunoglobulin heavy chain complex gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:20511552 1615753 Igh immunoglobulin heavy chain complex gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:22051050 1615753 Igh immunoglobulin heavy chain complex gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12668643 1615753 Igh immunoglobulin heavy chain complex gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16272317 1615753 Igh immunoglobulin heavy chain complex gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16860756 1615753 Igh immunoglobulin heavy chain complex gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:23940273 1615753 Igh immunoglobulin heavy chain complex gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9794392 1615753 Igh immunoglobulin heavy chain complex gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0008233 abnormal pro-B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16204304 1615753 Igh immunoglobulin heavy chain complex gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20190912 MGI PMID:31088898 1615753 Igh immunoglobulin heavy chain complex gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:15879114 1615753 Igh immunoglobulin heavy chain complex gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12471120 1615753 Igh immunoglobulin heavy chain complex gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:14962903 1615753 Igh immunoglobulin heavy chain complex gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15699070 1615753 Igh immunoglobulin heavy chain complex gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19615922 1615753 Igh immunoglobulin heavy chain complex gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20511552 1615753 Igh immunoglobulin heavy chain complex gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:24019479 1615753 Igh immunoglobulin heavy chain complex gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20230309 MGI PMID:29907762 1615753 Igh immunoglobulin heavy chain complex gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12471120 1615753 Igh immunoglobulin heavy chain complex gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20230309 MGI PMID:29907762 1615753 Igh immunoglobulin heavy chain complex gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:12471120 1615753 Igh immunoglobulin heavy chain complex gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:14962903 1615753 Igh immunoglobulin heavy chain complex gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20230309 MGI PMID:29907762 1615753 Igh immunoglobulin heavy chain complex gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:12471120 1615753 Igh immunoglobulin heavy chain complex gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:14962903 1615753 Igh immunoglobulin heavy chain complex gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:24019479 1615753 Igh immunoglobulin heavy chain complex gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12668643 1615753 Igh immunoglobulin heavy chain complex gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:17420268 1615753 Igh immunoglobulin heavy chain complex gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12668643 1615753 Igh immunoglobulin heavy chain complex gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:12668643 1615753 Igh immunoglobulin heavy chain complex gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:12668643 1615753 Igh immunoglobulin heavy chain complex gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:14758357 1615753 Igh immunoglobulin heavy chain complex gene MP:0008744 abnormal B cell anergy IAGP N RGD:5509061 20141003 MGI PMID:12668643 1615753 Igh immunoglobulin heavy chain complex gene MP:0008755 abnormal immunoglobulin V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:21909113 1615753 Igh immunoglobulin heavy chain complex gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:12471120 1615753 Igh immunoglobulin heavy chain complex gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:17082616 1615753 Igh immunoglobulin heavy chain complex gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:19050259 1615753 Igh immunoglobulin heavy chain complex gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:23254285 1615753 Igh immunoglobulin heavy chain complex gene MP:0008761 abnormal immunoglobulin light chain V-J recombination IAGP N RGD:5509061 20141003 MGI PMID:19114667 1615753 Igh immunoglobulin heavy chain complex gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11896394 1615753 Igh immunoglobulin heavy chain complex gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15735016 1615753 Igh immunoglobulin heavy chain complex gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19573810 1615753 Igh immunoglobulin heavy chain complex gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21623346 1615753 Igh immunoglobulin heavy chain complex gene MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15735016 1615753 Igh immunoglobulin heavy chain complex gene MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20393505 1615753 Igh immunoglobulin heavy chain complex gene MP:0010337 increased chronic lymphocytic leukemia incidence IAGP N RGD:5509061 20160707 MGI PMID:19332766 1615753 Igh immunoglobulin heavy chain complex gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:16973388 1615753 Igh immunoglobulin heavy chain complex gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:16973388 1615753 Igh immunoglobulin heavy chain complex gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:16973388 1615753 Igh immunoglobulin heavy chain complex gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16968900 1615753 Igh immunoglobulin heavy chain complex gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19573810 1615753 Igh immunoglobulin heavy chain complex gene MP:0014404 decreased late pro-B cell number IAGP N RGD:5509061 20240405 MGI PMID:19050258 1615753 Igh immunoglobulin heavy chain complex gene MP:0014470 abnormal B cell migration IAGP N RGD:5509061 20240613 MGI PMID:16286020 1615753 Igh immunoglobulin heavy chain complex gene MP:0014472 impaired B cell migration IAGP N RGD:5509061 20240613 MGI PMID:19615922 1615753 Igh immunoglobulin heavy chain complex gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20210520 MGI PMID:30289441 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:11921339 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:24095735 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24095735 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:11684658 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:11684658 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11684658 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11684658 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11921339 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11684658 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11921339 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11684658 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11921339 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:11921339 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11921339 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24095735 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24095735 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11684658 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:11684658 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:11684658 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:11684658 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:11921339 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0003143 enlarged otoliths IAGP N RGD:5509061 20141003 MGI PMID:11921339 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0003144 decreased otolith number IAGP N RGD:5509061 20141003 MGI PMID:11921339 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:24095735 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11684658 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0003946 renal necrosis IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:24095735 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24095735 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:11921339 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11921339 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11684658 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:7889565 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24095735 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11684658 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0011238 abnormal inner ear development IAGP N RGD:5509061 20240822 MGI PMID:11921339 1615754 Bcr BCR activator of RhoGEF and GTPase gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210211 MGI PMID:7889565 1615757 E2f8 E2F transcription factor 8 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:18194653 1615757 E2f8 E2F transcription factor 8 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:18194653 1615757 E2f8 E2F transcription factor 8 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:18194653 1615757 E2f8 E2F transcription factor 8 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:18194653 1615757 E2f8 E2F transcription factor 8 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:18194653 1615757 E2f8 E2F transcription factor 8 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:18194653 1615757 E2f8 E2F transcription factor 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:18194653 1615757 E2f8 E2F transcription factor 8 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0004259 small placenta IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0008402 increased cellular sensitivity to alkylating agents IAGP N RGD:5509061 20200310 MGI PMID:18194653 1615757 E2f8 E2F transcription factor 8 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0008959 abnormal spongiotrophoblast cell morphology IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0009658 increased placenta apoptosis IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18194653 1615757 E2f8 E2F transcription factor 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22516201 1615757 E2f8 E2F transcription factor 8 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:18194653 1615761 Lhfpl6 LHFPL tetraspan subfamily member 6 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1615761 Lhfpl6 LHFPL tetraspan subfamily member 6 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1615761 Lhfpl6 LHFPL tetraspan subfamily member 6 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1615761 Lhfpl6 LHFPL tetraspan subfamily member 6 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1615761 Lhfpl6 LHFPL tetraspan subfamily member 6 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1615761 Lhfpl6 LHFPL tetraspan subfamily member 6 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1615761 Lhfpl6 LHFPL tetraspan subfamily member 6 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1615763 Aida axin interactor, dorsalization associated gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0001261 obese IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20200409 MGI PMID:29617643 1615763 Aida axin interactor, dorsalization associated gene MP:0031269 increased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:29617643 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20241107 MGI 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20241017 MGI 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20241017 MGI 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20241017 MGI 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20241017 MGI 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20200310 MGI PMID:17334369 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20200310 MGI PMID:17334369 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20200310 MGI PMID:17334369 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0009331 absent primitive node IEA N RGD:5509061 20241017 MGI 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0009695 abnormal spinal cord ventral commissure morphology IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20241107 MGI 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0012724 absent head fold IEA N RGD:5509061 20241017 MGI 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20200310 MGI PMID:17334369 1615764 B4gat1 beta-1,4-glucuronyltransferase 1 gene MP:0020391 radial glial endfoot detachment IAGP N RGD:5509061 20200310 MGI PMID:23217742 1615765 Fam72a family with sequence similarity 72, member A gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1615765 Fam72a family with sequence similarity 72, member A gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20220721 MGI PMID:34819670 1615765 Fam72a family with sequence similarity 72, member A gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20220721 MGI PMID:34819670 1615765 Fam72a family with sequence similarity 72, member A gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 1615765 Fam72a family with sequence similarity 72, member A gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20220721 MGI PMID:34819670 1615765 Fam72a family with sequence similarity 72, member A gene MP:0008528 polycystic kidney IEA N RGD:5509061 20181227 MGI 1615765 Fam72a family with sequence similarity 72, member A gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20220721 MGI PMID:34819670 1615766 Rdh1 retinol dehydrogenase 1 (all trans) gene MP:0000683 decreased percent water in carcass IAGP N RGD:5509061 20141003 MGI PMID:17435174 1615766 Rdh1 retinol dehydrogenase 1 (all trans) gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:17435174 1615766 Rdh1 retinol dehydrogenase 1 (all trans) gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17435174 1615766 Rdh1 retinol dehydrogenase 1 (all trans) gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17435174 1615766 Rdh1 retinol dehydrogenase 1 (all trans) gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:17435174 1615766 Rdh1 retinol dehydrogenase 1 (all trans) gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17435174 1615766 Rdh1 retinol dehydrogenase 1 (all trans) gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17435174 1615766 Rdh1 retinol dehydrogenase 1 (all trans) gene MP:0011234 abnormal retinol level IAGP N RGD:5509061 20141003 MGI PMID:17435174 1615767 Srl sarcalumenin gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15569689 1615767 Srl sarcalumenin gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:15998745 1615767 Srl sarcalumenin gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15569689 1615767 Srl sarcalumenin gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:15569689 1615767 Srl sarcalumenin gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:15569689 1615767 Srl sarcalumenin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15569689 1615767 Srl sarcalumenin gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15569689 1615769 Tubg2 tubulin, gamma 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15893303 1615770 Tmem98 transmembrane protein 98 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1615770 Tmem98 transmembrane protein 98 gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20190829 MGI PMID:11929848 1615770 Tmem98 transmembrane protein 98 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20190912 MGI PMID:31266059 1615770 Tmem98 transmembrane protein 98 gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20190912 MGI PMID:31266059 1615770 Tmem98 transmembrane protein 98 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:31266059 1615770 Tmem98 transmembrane protein 98 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615770 Tmem98 transmembrane protein 98 gene MP:0012671 retina spots IAGP N RGD:5509061 20190829 MGI PMID:11929848 1615770 Tmem98 transmembrane protein 98 gene MP:0012671 retina spots IAGP N RGD:5509061 20230907 MGI PMID:37419942 1615770 Tmem98 transmembrane protein 98 gene MP:0021107 retina fold IAGP N RGD:5509061 20230907 MGI PMID:37419942 1615771 Tbc1d10a TBC1 domain family, member 10a gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:24652767 1615771 Tbc1d10a TBC1 domain family, member 10a gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20200310 MGI PMID:24652767 1615771 Tbc1d10a TBC1 domain family, member 10a gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:24652767 1615771 Tbc1d10a TBC1 domain family, member 10a gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20200310 MGI PMID:24652767 1615771 Tbc1d10a TBC1 domain family, member 10a gene MP:0010095 increased chromosomal stability IAGP N RGD:5509061 20200310 MGI PMID:24652767 1615773 Xylb xylulokinase homolog (H. influenzae) gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20200310 MGI 1615773 Xylb xylulokinase homolog (H. influenzae) gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200310 MGI 1615773 Xylb xylulokinase homolog (H. influenzae) gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20200310 MGI 1615773 Xylb xylulokinase homolog (H. influenzae) gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20200310 MGI 1615773 Xylb xylulokinase homolog (H. influenzae) gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200310 MGI 1615773 Xylb xylulokinase homolog (H. influenzae) gene MP:0005316 abnormal response to tactile stimuli IEA N RGD:5509061 20200310 MGI 1615775 Rpusd3 RNA pseudouridylate synthase domain containing 3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230601 MGI 1615775 Rpusd3 RNA pseudouridylate synthase domain containing 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20150129 MGI PMID:25180231 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20150129 MGI PMID:25180231 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20150129 MGI PMID:25180231 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210422 MGI PMID:33414192 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160915 MGI PMID:24652767 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210422 MGI PMID:33414192 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20200123 MGI PMID:28104815 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20150129 MGI PMID:25180231 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20160804 MGI 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200123 MGI PMID:28104815 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200123 MGI PMID:28104815 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20210422 MGI PMID:33414192 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20210422 MGI PMID:33414192 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20150129 MGI PMID:25180231 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20200123 MGI PMID:28104815 1615777 Ttll3 tubulin tyrosine ligase-like family, member 3 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210422 MGI PMID:33414192 1615778 Ifi44 interferon-induced protein 44 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20200310 MGI 1615778 Ifi44 interferon-induced protein 44 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20231207 MGI 1615778 Ifi44 interferon-induced protein 44 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1615778 Ifi44 interferon-induced protein 44 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20210304 MGI PMID:32611756 1615778 Ifi44 interferon-induced protein 44 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20210304 MGI PMID:32611756 1615778 Ifi44 interferon-induced protein 44 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1615778 Ifi44 interferon-induced protein 44 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20210304 MGI PMID:32611756 1615778 Ifi44 interferon-induced protein 44 gene MP:0031222 decreased CXCL10 secretion IAGP N RGD:5509061 20210304 MGI PMID:32611756 1615779 Arfip1 ADP-ribosylation factor interacting protein 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20201022 MGI 1615779 Arfip1 ADP-ribosylation factor interacting protein 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20201022 MGI 1615779 Arfip1 ADP-ribosylation factor interacting protein 1 gene MP:0001147 small testis IEA N RGD:5509061 20201022 MGI 1615779 Arfip1 ADP-ribosylation factor interacting protein 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20201022 MGI 1615779 Arfip1 ADP-ribosylation factor interacting protein 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1615781 Mael maelstrom spermatogenic transposon silencer gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:18694567 1615781 Mael maelstrom spermatogenic transposon silencer gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:18694567 1615781 Mael maelstrom spermatogenic transposon silencer gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20200310 MGI PMID:18694567 1615781 Mael maelstrom spermatogenic transposon silencer gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:18694567 1615781 Mael maelstrom spermatogenic transposon silencer gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20200310 MGI PMID:18694567 1615781 Mael maelstrom spermatogenic transposon silencer gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:18694567 1615784 Zbtb22 zinc finger and BTB domain containing 22 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20240418 MGI PMID:37154299 1615784 Zbtb22 zinc finger and BTB domain containing 22 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20240418 MGI PMID:37154299 1615784 Zbtb22 zinc finger and BTB domain containing 22 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20240418 MGI PMID:37154299 1615784 Zbtb22 zinc finger and BTB domain containing 22 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20240418 MGI PMID:37154299 1615784 Zbtb22 zinc finger and BTB domain containing 22 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20240418 MGI PMID:37154299 1615784 Zbtb22 zinc finger and BTB domain containing 22 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20240418 MGI PMID:37154299 1615784 Zbtb22 zinc finger and BTB domain containing 22 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240418 MGI PMID:37154299 1615784 Zbtb22 zinc finger and BTB domain containing 22 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20240418 MGI PMID:37154299 1615784 Zbtb22 zinc finger and BTB domain containing 22 gene MP:0009122 decreased white fat cell lipid droplet size IAGP N RGD:5509061 20240418 MGI PMID:37154299 1615784 Zbtb22 zinc finger and BTB domain containing 22 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20240418 MGI PMID:37154299 1615784 Zbtb22 zinc finger and BTB domain containing 22 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20240418 MGI PMID:37154299 1615784 Zbtb22 zinc finger and BTB domain containing 22 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20240418 MGI PMID:37154299 1615784 Zbtb22 zinc finger and BTB domain containing 22 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20240418 MGI PMID:37154299 1615784 Zbtb22 zinc finger and BTB domain containing 22 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240418 MGI PMID:37154299 1615785 Chia1 chitinase, acidic 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:21836154 1615785 Chia1 chitinase, acidic 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20200310 MGI 1615785 Chia1 chitinase, acidic 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:21836154 1615785 Chia1 chitinase, acidic 1 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20200310 MGI PMID:21836154 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0000746 weakness IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0001147 small testis IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0002083 premature death IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0002997 enlarged seminal vesicle IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0003786 premature aging IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0008676 decreased interleukin-15 secretion IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0010138 arteritis IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0010138 arteritis IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0011117 abnormal susceptibility to weight gain IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0011508 abnormal glomerular capillary thrombosis IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0011508 abnormal glomerular capillary thrombosis IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0013249 adipose tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:17318811 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0013600 testis degeneration IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0031210 small cauda epididymis IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615786 Tusc2 tumor suppressor 2, mitochondrial calcium regulator gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20220929 MGI PMID:28351997 1615787 Tex21 testis expressed gene 21 gene MP:0001406 abnormal gait IEA N RGD:5509061 20231207 MGI 1615787 Tex21 testis expressed gene 21 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1615787 Tex21 testis expressed gene 21 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210826 MGI 1615787 Tex21 testis expressed gene 21 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1615787 Tex21 testis expressed gene 21 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220519 MGI 1615791 Dcst1 DC-STAMP domain containing 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20210520 MGI PMID:33871360 1615791 Dcst1 DC-STAMP domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20210520 MGI PMID:33871360 1615793 Rnf170 ring finger protein 170 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20170831 MGI PMID:26433933 1615793 Rnf170 ring finger protein 170 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20170831 MGI PMID:26433933 1615793 Rnf170 ring finger protein 170 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20170831 MGI PMID:26433933 1615793 Rnf170 ring finger protein 170 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20170831 MGI PMID:26433933 1615793 Rnf170 ring finger protein 170 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20170831 MGI PMID:26433933 1615794 6030468B19Rik RIKEN cDNA 6030468B19 gene gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170323 MGI 1615796 Abcb5 ATP-binding cassette, sub-family B member 5 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20181101 MGI PMID:25030174 1615796 Abcb5 ATP-binding cassette, sub-family B member 5 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20181101 MGI PMID:25030174 1615796 Abcb5 ATP-binding cassette, sub-family B member 5 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20181101 MGI PMID:25030174 1615796 Abcb5 ATP-binding cassette, sub-family B member 5 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20181101 MGI PMID:25030174 1615796 Abcb5 ATP-binding cassette, sub-family B member 5 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20181101 MGI PMID:25030174 1615796 Abcb5 ATP-binding cassette, sub-family B member 5 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20181101 MGI PMID:25030174 1615796 Abcb5 ATP-binding cassette, sub-family B member 5 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20181101 MGI PMID:25030174 1615796 Abcb5 ATP-binding cassette, sub-family B member 5 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20181101 MGI PMID:25030174 1615796 Abcb5 ATP-binding cassette, sub-family B member 5 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20181101 MGI PMID:25030174 1615796 Abcb5 ATP-binding cassette, sub-family B member 5 gene MP:0020858 cornea epithelium hypoplasia IAGP N RGD:5509061 20181101 MGI PMID:25030174 1615796 Abcb5 ATP-binding cassette, sub-family B member 5 gene MP:0020861 abnormal cornea wound healing IAGP N RGD:5509061 20181101 MGI PMID:25030174 1615797 Cstdc2 cystatin domain containing 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1615797 Cstdc2 cystatin domain containing 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1615797 Cstdc2 cystatin domain containing 2 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 1615799 Kndc1 kinase non-catalytic C-lobe domain (KIND) containing 1 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20190131 MGI PMID:28264072 1615799 Kndc1 kinase non-catalytic C-lobe domain (KIND) containing 1 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20190131 MGI PMID:28264072 1615799 Kndc1 kinase non-catalytic C-lobe domain (KIND) containing 1 gene MP:0004099 abnormal cerebellar glomerulus morphology IAGP N RGD:5509061 20190131 MGI PMID:28264072 1615799 Kndc1 kinase non-catalytic C-lobe domain (KIND) containing 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20190131 MGI PMID:28264072 1615799 Kndc1 kinase non-catalytic C-lobe domain (KIND) containing 1 gene MP:0010052 increased grip strength IAGP N RGD:5509061 20190131 MGI PMID:28264072 1615799 Kndc1 kinase non-catalytic C-lobe domain (KIND) containing 1 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20190131 MGI PMID:28264072 1615799 Kndc1 kinase non-catalytic C-lobe domain (KIND) containing 1 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20190131 MGI PMID:28264072 1615800 Pcolce2 procollagen C-endopeptidase enhancer 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17683113 1615801 Knl1 kinetochore scaffold 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615801 Knl1 kinetochore scaffold 1 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615801 Knl1 kinetochore scaffold 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615801 Knl1 kinetochore scaffold 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615801 Knl1 kinetochore scaffold 1 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615801 Knl1 kinetochore scaffold 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615801 Knl1 kinetochore scaffold 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615801 Knl1 kinetochore scaffold 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1615801 Knl1 kinetochore scaffold 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615801 Knl1 kinetochore scaffold 1 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615801 Knl1 kinetochore scaffold 1 gene MP:0008762 embryonic lethality IEA N RGD:5509061 20141003 MGI 1615801 Knl1 kinetochore scaffold 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615801 Knl1 kinetochore scaffold 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615801 Knl1 kinetochore scaffold 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615801 Knl1 kinetochore scaffold 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615801 Knl1 kinetochore scaffold 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615801 Knl1 kinetochore scaffold 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615801 Knl1 kinetochore scaffold 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20141003 MGI 1615801 Knl1 kinetochore scaffold 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615801 Knl1 kinetochore scaffold 1 gene MP:0013289 abnormal mitotic cytokinesis IAGP N RGD:5509061 20190912 MGI PMID:31197172 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20180315 MGI PMID:29115376 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20180315 MGI PMID:29115376 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0000601 small liver IAGP N RGD:5509061 20180315 MGI PMID:29115376 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0001577 anemia IAGP N RGD:5509061 20180315 MGI PMID:29115376 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20180315 MGI PMID:29115376 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20180315 MGI PMID:29115376 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180315 MGI PMID:29115376 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20180315 MGI PMID:29115376 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180315 MGI PMID:29115376 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20180315 MGI PMID:29115376 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0004259 small placenta IAGP N RGD:5509061 20180315 MGI PMID:29115376 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20180315 MGI PMID:29115376 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20180315 MGI PMID:29115376 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180315 MGI PMID:29115376 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1615802 Ccdc134 coiled-coil domain containing 134 gene MP:0011526 abnormal placenta fetal blood space morphology IAGP N RGD:5509061 20180315 MGI PMID:29115376 1615807 1700028K03Rik RIKEN cDNA 1700028K03 gene gene MP:0001127 small ovary IAGP N RGD:5509061 20200416 MGI PMID:30949703 1615807 1700028K03Rik RIKEN cDNA 1700028K03 gene gene MP:0001147 small testis IAGP N RGD:5509061 20200416 MGI PMID:30949703 1615807 1700028K03Rik RIKEN cDNA 1700028K03 gene gene MP:0001925 male infertility IAGP N RGD:5509061 20200416 MGI PMID:30949703 1615807 1700028K03Rik RIKEN cDNA 1700028K03 gene gene MP:0001926 female infertility IAGP N RGD:5509061 20200416 MGI PMID:30949703 1615807 1700028K03Rik RIKEN cDNA 1700028K03 gene gene MP:0004805 absent oocytes IAGP N RGD:5509061 20200416 MGI PMID:30949703 1615807 1700028K03Rik RIKEN cDNA 1700028K03 gene gene MP:0005159 azoospermia IAGP N RGD:5509061 20200416 MGI PMID:30949703 1615807 1700028K03Rik RIKEN cDNA 1700028K03 gene gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20200416 MGI PMID:30949703 1615807 1700028K03Rik RIKEN cDNA 1700028K03 gene gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20200416 MGI PMID:30949703 1615807 1700028K03Rik RIKEN cDNA 1700028K03 gene gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20200416 MGI PMID:30949703 1615807 1700028K03Rik RIKEN cDNA 1700028K03 gene gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20200416 MGI PMID:30949703 1615807 1700028K03Rik RIKEN cDNA 1700028K03 gene gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20200416 MGI PMID:30949703 1615808 Cimap3 ciliary microtubule associated protein 3 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:20643351 1615808 Cimap3 ciliary microtubule associated protein 3 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:20643351 1615808 Cimap3 ciliary microtubule associated protein 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20643351 1615808 Cimap3 ciliary microtubule associated protein 3 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20643351 1615808 Cimap3 ciliary microtubule associated protein 3 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:20643351 1615808 Cimap3 ciliary microtubule associated protein 3 gene MP:0004131 abnormal motile primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:20643351 1615808 Cimap3 ciliary microtubule associated protein 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20643351 1615808 Cimap3 ciliary microtubule associated protein 3 gene MP:0008933 abnormal motile primary cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:20643351 1615808 Cimap3 ciliary microtubule associated protein 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20643351 1615808 Cimap3 ciliary microtubule associated protein 3 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:20643351 1615813 Saxo5 stabilizer of axonemal microtubules 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1615817 Meiob meiosis specific with OB domains gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:24068956 1615817 Meiob meiosis specific with OB domains gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:24068956 1615817 Meiob meiosis specific with OB domains gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:24068956 1615817 Meiob meiosis specific with OB domains gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:24068956 1615817 Meiob meiosis specific with OB domains gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:24068956 1615817 Meiob meiosis specific with OB domains gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:24068956 1615817 Meiob meiosis specific with OB domains gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:24068956 1615817 Meiob meiosis specific with OB domains gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:24068956 1615817 Meiob meiosis specific with OB domains gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:24068956 1615817 Meiob meiosis specific with OB domains gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:24068956 1615817 Meiob meiosis specific with OB domains gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:24068956 1615817 Meiob meiosis specific with OB domains gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20201015 MGI PMID:32345962 1615817 Meiob meiosis specific with OB domains gene MP:0013507 increased ovary apoptosis IAGP N RGD:5509061 20160428 MGI PMID:24068956 1615817 Meiob meiosis specific with OB domains gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:24068956 1615818 Tex38 testis expressed 38 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200402 MGI 1615818 Tex38 testis expressed 38 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1615818 Tex38 testis expressed 38 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200402 MGI 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0001925 male infertility IAGP N RGD:5509061 20240208 MGI PMID:38038747 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20240208 MGI PMID:38038747 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240208 MGI PMID:38038747 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20240208 MGI PMID:38038747 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20240208 MGI PMID:38038747 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20240208 MGI PMID:38038747 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240208 MGI PMID:38038747 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20240208 MGI PMID:38038747 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20240208 MGI PMID:38038747 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20240208 MGI PMID:38038747 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20240208 MGI PMID:38038747 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20240208 MGI PMID:38038747 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20240208 MGI PMID:38038747 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0031373 abnormal manchette perinuclear ring morphology IAGP N RGD:5509061 20240208 MGI PMID:38038747 1615819 Ccdc146 coiled-coil domain containing 146 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20240208 MGI PMID:38038747 1615822 Slxl1 Slx-like 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20210819 MGI PMID:31630956 1615822 Slxl1 Slx-like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20210819 MGI PMID:31630956 1615822 Slxl1 Slx-like 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20210819 MGI PMID:31630956 1615822 Slxl1 Slx-like 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210819 MGI PMID:31630956 1615822 Slxl1 Slx-like 1 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20210819 MGI PMID:31630956 1615822 Slxl1 Slx-like 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210819 MGI PMID:31630956 1615828 Zdbf2 zinc finger, DBF-type containing 2 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1615828 Zdbf2 zinc finger, DBF-type containing 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180712 MGI PMID:27841881 1615828 Zdbf2 zinc finger, DBF-type containing 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180712 MGI PMID:27841881 1615828 Zdbf2 zinc finger, DBF-type containing 2 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20180712 MGI PMID:27841881 1615833 Tmem198b transmembrane protein 198b gene MP:0002635 reduced sensorimotor gating IEA N RGD:5509061 20170323 MGI 1615834 Ppp1r21 protein phosphatase 1, regulatory subunit 21 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0000371 diluted coat color IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0000454 abnormal jaw morphology IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0000585 kinked tail IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0001259 abnormal body weight IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0001262 decreased body weight IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0001265 decreased body size IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0001928 abnormal ovulation IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0002083 premature death IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0002089 abnormal postnatal growth/weight/body size IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0002116 abnormal craniofacial bone morphology IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0003355 decreased ovulation rate IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20171116 MGI PMID:2778559 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0005171 absent coat pigmentation IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0005508 abnormal skeleton morphology IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20171116 MGI 1615836 Mfsd12 major facilitator superfamily domain containing 12 gene MP:0012017 grizzled coat color IAGP N RGD:5509061 20171116 MGI PMID:29025994 1615838 Tex36 testis expressed 36 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1615838 Tex36 testis expressed 36 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1615838 Tex36 testis expressed 36 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210708 MGI PMID:32561905 1615842 Shisa9 shisa family member 9 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1615842 Shisa9 shisa family member 9 gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20180412 MGI PMID:29343769 1615842 Shisa9 shisa family member 9 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20180412 MGI PMID:29343769 1615842 Shisa9 shisa family member 9 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20180412 MGI PMID:20185686 1615842 Shisa9 shisa family member 9 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20180412 MGI PMID:29343769 1615842 Shisa9 shisa family member 9 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200514 MGI 1615842 Shisa9 shisa family member 9 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20180412 MGI PMID:29343769 1615842 Shisa9 shisa family member 9 gene MP:0011267 abnormal excitatory postsynaptic current amplitude IAGP N RGD:5509061 20180412 MGI PMID:29343769 1615843 Tagap T cell activation Rho GTPase activating protein gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:16116428 1615843 Tagap T cell activation Rho GTPase activating protein gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:16116428 1615843 Tagap T cell activation Rho GTPase activating protein gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16116428 1615843 Tagap T cell activation Rho GTPase activating protein gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:16116428 1615844 Atxn7l2 ataxin 7-like 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20240523 MGI 1615844 Atxn7l2 ataxin 7-like 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1615844 Atxn7l2 ataxin 7-like 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1615844 Atxn7l2 ataxin 7-like 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1615844 Atxn7l2 ataxin 7-like 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1615844 Atxn7l2 ataxin 7-like 2 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20231207 MGI 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20231207 MGI 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20190523 MGI PMID:28951494 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20190523 MGI PMID:28951494 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20190523 MGI PMID:28951494 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20190523 MGI PMID:28951494 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190207 MGI PMID:26880576 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190207 MGI PMID:26880576 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:23989956 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23989956 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20190523 MGI PMID:28951494 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0001924 infertility IAGP N RGD:5509061 20190207 MGI PMID:26880576 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0001926 female infertility IEA N RGD:5509061 20231207 MGI 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20190523 MGI PMID:28951494 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23989956 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:18724357 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:23989956 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20190523 MGI PMID:28951494 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0002938 white spotting IAGP N RGD:5509061 20190207 MGI PMID:26880576 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:21098106 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38786026 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20190207 MGI PMID:26880576 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20190523 MGI PMID:28951494 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20190523 MGI PMID:28951494 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:23989956 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20141003 MGI PMID:21098106 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20141003 MGI PMID:21813776 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20141003 MGI PMID:23989956 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20190523 MGI PMID:28951494 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21813776 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0008608 increased circulating interleukin-13 level IAGP N RGD:5509061 20190523 MGI PMID:28951494 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20190523 MGI PMID:28951494 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0008731 abnormal hair shaft melanin granule morphology IAGP N RGD:5509061 20190207 MGI PMID:26880576 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23989956 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0010334 pleural effusion IAGP N RGD:5509061 20190523 MGI PMID:28951494 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20190207 MGI PMID:26880576 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20190523 MGI PMID:28951494 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20190523 MGI PMID:28951494 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0014234 decreased enterocyte apoptosis IAGP N RGD:5509061 20230323 MGI PMID:30254094 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:18724357 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0020915 abnormal susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:18724357 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:23989956 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:29871919 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:23989956 1615847 Sting1 stimulator of interferon response cGAMP interactor 1 gene MP:0031167 abnormal lung thrombosis IAGP N RGD:5509061 20201210 MGI PMID:28951494 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:11557891 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20220512 MGI PMID:19684329 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001127 small ovary IAGP N RGD:5509061 20200310 MGI PMID:11557891 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20200310 MGI PMID:11557891 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220512 MGI PMID:17207475 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20200310 MGI PMID:11557891 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:15774719 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20200310 MGI PMID:15774719 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:15774719 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:15774719 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:15774719 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220512 MGI PMID:19684329 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001925 male infertility IAGP N RGD:5509061 20220512 MGI PMID:15774719 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:11557891 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20220512 MGI PMID:19684329 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20200310 MGI PMID:15774719 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0002016 ovary cyst IAGP N RGD:5509061 20220512 MGI PMID:19684329 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:15774719 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20200310 MGI PMID:15774719 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:15774719 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20220512 MGI PMID:19684329 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0003378 early sexual maturation IAGP N RGD:5509061 20220512 MGI PMID:19684329 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:15774719 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200310 MGI PMID:15774719 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20220512 MGI PMID:19684329 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20200310 MGI PMID:15774719 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20220512 MGI PMID:19684329 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0009648 abnormal superovulation IAGP N RGD:5509061 20220512 MGI PMID:11557891 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220512 MGI PMID:17207475 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0011127 abnormal tertiary ovarian follicle number IAGP N RGD:5509061 20220512 MGI PMID:17207475 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220512 MGI PMID:17207475 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0013236 ovary degeneration IAGP N RGD:5509061 20220512 MGI PMID:19684329 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20220512 MGI PMID:17207475 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0031018 decreased granulosa cell proliferation IAGP N RGD:5509061 20220512 MGI PMID:17207475 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20220512 MGI PMID:19684329 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220512 MGI PMID:17207475 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220512 MGI PMID:15774719 1615849 Taf4b TATA-box binding protein associated factor 4b gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220512 MGI PMID:17207475 1615850 Crnde colorectal neoplasia differentially expressed, non-protein coding gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24381249 1615852 Ccdc57 coiled-coil domain containing 57 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20160804 MGI 1615852 Ccdc57 coiled-coil domain containing 57 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1615852 Ccdc57 coiled-coil domain containing 57 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160804 MGI 1615852 Ccdc57 coiled-coil domain containing 57 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1615852 Ccdc57 coiled-coil domain containing 57 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20160804 MGI 1615852 Ccdc57 coiled-coil domain containing 57 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160804 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20141003 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20150806 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20150806 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0000644 dextrocardia IEA N RGD:5509061 20141003 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0000690 absent spleen IEA N RGD:5509061 20150806 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20141003 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0002745 abnormal atrioventricular valve morphology IEA N RGD:5509061 20150806 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0003178 left pulmonary isomerism IEA N RGD:5509061 20141003 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0004113 abnormal aortic arch morphology IEA N RGD:5509061 20150806 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0004158 right aortic arch IEA N RGD:5509061 20150806 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20150806 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141003 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20141003 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0010808 right-sided stomach IEA N RGD:5509061 20141003 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0011055 abnormal respiratory motile cilium physiology IEA N RGD:5509061 20141003 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0011250 abdominal situs ambiguus IEA N RGD:5509061 20141003 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0011252 situs inversus totalis IEA N RGD:5509061 20141003 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0011649 immotile respiratory cilia IEA N RGD:5509061 20141003 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20150806 MGI 1615857 Daw1 dynein assembly factor with WDR repeat domains 1 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20141003 MGI 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:23661644 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23661644 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20200402 MGI 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23661644 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23661644 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:23661644 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20201022 MGI 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23661644 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23661644 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:23661644 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23661644 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:23661644 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23661644 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23661644 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20200402 MGI 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20201022 MGI 1615859 Gpr15 G protein-coupled receptor 15 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:23661644 1615861 Rsc1a1 regulatory solute carrier protein, family 1, member 1 gene MP:0000676 abnormal body water content IAGP N RGD:5509061 20141003 MGI PMID:15601832 1615861 Rsc1a1 regulatory solute carrier protein, family 1, member 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15601832 1615861 Rsc1a1 regulatory solute carrier protein, family 1, member 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15601832 1615861 Rsc1a1 regulatory solute carrier protein, family 1, member 1 gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:15601832 1615861 Rsc1a1 regulatory solute carrier protein, family 1, member 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15601832 1615861 Rsc1a1 regulatory solute carrier protein, family 1, member 1 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15601832 1615861 Rsc1a1 regulatory solute carrier protein, family 1, member 1 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:15601832 1615861 Rsc1a1 regulatory solute carrier protein, family 1, member 1 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:15601832 1615861 Rsc1a1 regulatory solute carrier protein, family 1, member 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15601832 1615861 Rsc1a1 regulatory solute carrier protein, family 1, member 1 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:15601832 1615861 Rsc1a1 regulatory solute carrier protein, family 1, member 1 gene MP:0013758 increased intestinal glucose absorption IAGP N RGD:5509061 20191031 MGI PMID:15601832 1615864 Sis sucrase isomaltase gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1615864 Sis sucrase isomaltase gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1615864 Sis sucrase isomaltase gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20240404 MGI PMID:34914943 1615864 Sis sucrase isomaltase gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20240404 MGI PMID:34914943 1615864 Sis sucrase isomaltase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20240404 MGI PMID:34914943 1615864 Sis sucrase isomaltase gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20240404 MGI PMID:34914943 1615864 Sis sucrase isomaltase gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20240404 MGI PMID:34914943 1615864 Sis sucrase isomaltase gene MP:0012347 low sweet preference IAGP N RGD:5509061 20240404 MGI PMID:34914943 1615866 Zfp715 zinc finger protein 715 gene MP:0003062 abnormal coping response IEA N RGD:5509061 20160804 MGI 1615866 Zfp715 zinc finger protein 715 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1615866 Zfp715 zinc finger protein 715 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1615867 Agk acylglycerol kinase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:31204281 1615867 Agk acylglycerol kinase gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:31204281 1615867 Agk acylglycerol kinase gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:31204281 1615867 Agk acylglycerol kinase gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:31204281 1615867 Agk acylglycerol kinase gene MP:0010851 decreased effector memory CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:31204281 1615869 Hddc3 HD domain containing 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200310 MGI 1615869 Hddc3 HD domain containing 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20200310 MGI 1615869 Hddc3 HD domain containing 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200310 MGI 1615869 Hddc3 HD domain containing 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200310 MGI 1615869 Hddc3 HD domain containing 3 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1615869 Hddc3 HD domain containing 3 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20200310 MGI 1615869 Hddc3 HD domain containing 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200310 MGI 1615869 Hddc3 HD domain containing 3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1615869 Hddc3 HD domain containing 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1615872 Kansl1l KAT8 regulatory NSL complex subunit 1-like gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1615872 Kansl1l KAT8 regulatory NSL complex subunit 1-like gene MP:0001148 enlarged testis IEA N RGD:5509061 20210826 MGI 1615872 Kansl1l KAT8 regulatory NSL complex subunit 1-like gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210826 MGI 1615872 Kansl1l KAT8 regulatory NSL complex subunit 1-like gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20210826 MGI 1615872 Kansl1l KAT8 regulatory NSL complex subunit 1-like gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1615872 Kansl1l KAT8 regulatory NSL complex subunit 1-like gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1615872 Kansl1l KAT8 regulatory NSL complex subunit 1-like gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210826 MGI 1615873 Slc44a2 solute carrier family 44, member 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20200310 MGI PMID:26463873 1615873 Slc44a2 solute carrier family 44, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:26463873 1615873 Slc44a2 solute carrier family 44, member 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1615873 Slc44a2 solute carrier family 44, member 2 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1615873 Slc44a2 solute carrier family 44, member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:26463873 1615873 Slc44a2 solute carrier family 44, member 2 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:26463873 1615873 Slc44a2 solute carrier family 44, member 2 gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20200310 MGI PMID:26463873 1615873 Slc44a2 solute carrier family 44, member 2 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20200310 MGI PMID:26463873 1615873 Slc44a2 solute carrier family 44, member 2 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20200310 MGI PMID:26463873 1615873 Slc44a2 solute carrier family 44, member 2 gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20200310 MGI PMID:26463873 1615873 Slc44a2 solute carrier family 44, member 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:26463873 1615873 Slc44a2 solute carrier family 44, member 2 gene MP:0013808 abnormal tunnel of Corti morphology IAGP N RGD:5509061 20200310 MGI PMID:26463873 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0000111 cleft palate IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20231207 MGI 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20231207 MGI 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0000709 enlarged thymus IEA N RGD:5509061 20231207 MGI 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0000914 exencephaly IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0001265 decreased body size IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0001394 circling IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0001921 reduced fertility IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20230727 MGI PMID:35129866 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0002252 abnormal oropharynx morphology IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0002286 cryptorchism IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0002833 increased heart weight IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0002939 head spot IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20230216 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0003402 decreased liver weight IEA N RGD:5509061 20231207 MGI 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0005188 small penis IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0005652 sex reversal IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0009085 abnormal uterine horn morphology IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0010059 olfactory bulb hypoplasia IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0010715 retina coloboma IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0012535 abnormal optic fissure closure IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0012741 decreased neural crest cell proliferation IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0012744 increased neural crest cell apoptosis IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0013678 decreased Ly6C-positive NK T cell number IEA N RGD:5509061 20231207 MGI 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20231207 MGI 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0030099 facial asymmetry IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615875 Arb2a ARB2 cotranscriptional regulator A gene MP:0030393 delayed fontanelle closure IAGP N RGD:5509061 20230209 MGI PMID:29311329 1615877 Klk5 kallikrein related-peptidase 5 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210128 MGI 1615877 Klk5 kallikrein related-peptidase 5 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1615877 Klk5 kallikrein related-peptidase 5 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20240523 MGI 1615877 Klk5 kallikrein related-peptidase 5 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1615877 Klk5 kallikrein related-peptidase 5 gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20240404 MGI PMID:32461336 1615877 Klk5 kallikrein related-peptidase 5 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1615877 Klk5 kallikrein related-peptidase 5 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20210128 MGI 1615877 Klk5 kallikrein related-peptidase 5 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20210128 MGI 1615877 Klk5 kallikrein related-peptidase 5 gene MP:0004357 long tibia IEA N RGD:5509061 20210128 MGI 1615877 Klk5 kallikrein related-peptidase 5 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1615877 Klk5 kallikrein related-peptidase 5 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1615877 Klk5 kallikrein related-peptidase 5 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1615877 Klk5 kallikrein related-peptidase 5 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20210128 MGI 1615877 Klk5 kallikrein related-peptidase 5 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20240404 MGI PMID:32461336 1615877 Klk5 kallikrein related-peptidase 5 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1615879 Mtcl1 microtubule crosslinking factor 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20180517 MGI PMID:28283581 1615879 Mtcl1 microtubule crosslinking factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180517 MGI PMID:28283581 1615879 Mtcl1 microtubule crosslinking factor 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20180517 MGI PMID:28283581 1615879 Mtcl1 microtubule crosslinking factor 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20180517 MGI PMID:28283581 1615879 Mtcl1 microtubule crosslinking factor 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20180517 MGI PMID:28283581 1615879 Mtcl1 microtubule crosslinking factor 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20180517 MGI PMID:28283581 1615879 Mtcl1 microtubule crosslinking factor 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20180517 MGI PMID:28283581 1615879 Mtcl1 microtubule crosslinking factor 1 gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20180517 MGI PMID:28283581 1615879 Mtcl1 microtubule crosslinking factor 1 gene MP:0010733 abnormal axon initial segment morphology IAGP N RGD:5509061 20180517 MGI PMID:28283581 1615879 Mtcl1 microtubule crosslinking factor 1 gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:28283581 1615882 Bag4 BCL2-associated athanogene 4 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12748303 1615882 Bag4 BCL2-associated athanogene 4 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12748303 1615882 Bag4 BCL2-associated athanogene 4 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12748303 1615882 Bag4 BCL2-associated athanogene 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12944486 1615882 Bag4 BCL2-associated athanogene 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12748303 1615882 Bag4 BCL2-associated athanogene 4 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:12748303 1615882 Bag4 BCL2-associated athanogene 4 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:12748303 1615884 Jam2 junction adhesion molecule 2 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21868569 1615884 Jam2 junction adhesion molecule 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1615884 Jam2 junction adhesion molecule 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16914739 1615884 Jam2 junction adhesion molecule 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21868569 1615884 Jam2 junction adhesion molecule 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1615884 Jam2 junction adhesion molecule 2 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:21868569 1615884 Jam2 junction adhesion molecule 2 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21868569 1615884 Jam2 junction adhesion molecule 2 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:21868569 1615884 Jam2 junction adhesion molecule 2 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20220519 MGI 1615884 Jam2 junction adhesion molecule 2 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220519 MGI 1615884 Jam2 junction adhesion molecule 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20180322 MGI PMID:29114073 1615884 Jam2 junction adhesion molecule 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21868569 1615884 Jam2 junction adhesion molecule 2 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21868569 1615885 Paxbp1 PAX3 and PAX7 binding protein 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20211209 MGI PMID:33753492 1615885 Paxbp1 PAX3 and PAX7 binding protein 1 gene MP:0006039 decreased mitochondrial fission IAGP N RGD:5509061 20211209 MGI PMID:33753492 1615885 Paxbp1 PAX3 and PAX7 binding protein 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20211209 MGI PMID:33753492 1615885 Paxbp1 PAX3 and PAX7 binding protein 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20211209 MGI PMID:33753492 1615885 Paxbp1 PAX3 and PAX7 binding protein 1 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20211209 MGI PMID:33753492 1615885 Paxbp1 PAX3 and PAX7 binding protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20211209 MGI PMID:33753492 1615885 Paxbp1 PAX3 and PAX7 binding protein 1 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211209 MGI PMID:33753492 1615887 1700093K21Rik RIKEN cDNA 1700093K21 gene gene MP:0000644 dextrocardia IEA N RGD:5509061 20170209 MGI 1615887 1700093K21Rik RIKEN cDNA 1700093K21 gene gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1615887 1700093K21Rik RIKEN cDNA 1700093K21 gene gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1615887 1700093K21Rik RIKEN cDNA 1700093K21 gene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1615887 1700093K21Rik RIKEN cDNA 1700093K21 gene gene MP:0003047 abnormal thoracic vertebrae morphology IEA N RGD:5509061 20170209 MGI 1615887 1700093K21Rik RIKEN cDNA 1700093K21 gene gene MP:0004133 heterotaxia IEA N RGD:5509061 20170209 MGI 1615887 1700093K21Rik RIKEN cDNA 1700093K21 gene gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20170209 MGI 1615887 1700093K21Rik RIKEN cDNA 1700093K21 gene gene MP:0010808 right-sided stomach IEA N RGD:5509061 20170209 MGI 1615887 1700093K21Rik RIKEN cDNA 1700093K21 gene gene MP:0011250 abdominal situs ambiguus IEA N RGD:5509061 20170209 MGI 1615888 Tmco5 transmembrane and coiled-coil domains 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1615888 Tmco5 transmembrane and coiled-coil domains 5 gene MP:0003896 prolonged PR interval IEA N RGD:5509061 20240523 MGI 1615890 Spmip10 sperm microtubule inner protein 10 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20220120 MGI PMID:34446558 1615892 Ascl4 achaete-scute family bHLH transcription factor 4 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1615892 Ascl4 achaete-scute family bHLH transcription factor 4 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20220519 MGI 1615895 Spata31g1 SPATA31 subfamily G member 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20231109 MGI PMID:36871790 1615896 Inava innate immunity activator gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20210415 MGI PMID:29420262 1615896 Inava innate immunity activator gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20210415 MGI PMID:29420262 1615896 Inava innate immunity activator gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20210415 MGI PMID:29420262 1615896 Inava innate immunity activator gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20210415 MGI PMID:29420262 1615896 Inava innate immunity activator gene MP:0011804 increased cell migration IAGP N RGD:5509061 20210415 MGI PMID:29420262 1615896 Inava innate immunity activator gene MP:0014201 abnormal intestinal epithelium physiology IAGP N RGD:5509061 20210415 MGI PMID:29420262 1615897 Pbld2 phenazine biosynthesis-like protein domain containing 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1615897 Pbld2 phenazine biosynthesis-like protein domain containing 2 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210520 MGI 1615899 Ypel3 yippee like 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20230601 MGI 1615899 Ypel3 yippee like 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1615899 Ypel3 yippee like 3 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20230601 MGI 1615899 Ypel3 yippee like 3 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20211021 MGI 1615899 Ypel3 yippee like 3 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20231207 MGI 1615899 Ypel3 yippee like 3 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220519 MGI 1615899 Ypel3 yippee like 3 gene MP:0002764 short tibia IEA N RGD:5509061 20160114 MGI 1615899 Ypel3 yippee like 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1615899 Ypel3 yippee like 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1615899 Ypel3 yippee like 3 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 1615900 Tmem42 transmembrane protein 42 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20181227 MGI 1615900 Tmem42 transmembrane protein 42 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1615900 Tmem42 transmembrane protein 42 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 1615900 Tmem42 transmembrane protein 42 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1615901 Aurkaip1 aurora kinase A interacting protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615901 Aurkaip1 aurora kinase A interacting protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1615902 Tmem167 transmembrane protein 167 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20141003 MGI 1615902 Tmem167 transmembrane protein 167 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20160804 MGI 1615902 Tmem167 transmembrane protein 167 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160804 MGI 1615902 Tmem167 transmembrane protein 167 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160804 MGI 1615904 Cystm1 cysteine-rich transmembrane module containing 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1615904 Cystm1 cysteine-rich transmembrane module containing 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20170105 MGI 1615904 Cystm1 cysteine-rich transmembrane module containing 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210128 MGI 1615904 Cystm1 cysteine-rich transmembrane module containing 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1615904 Cystm1 cysteine-rich transmembrane module containing 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1615904 Cystm1 cysteine-rich transmembrane module containing 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1615904 Cystm1 cysteine-rich transmembrane module containing 1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20160811 MGI 1615904 Cystm1 cysteine-rich transmembrane module containing 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1615904 Cystm1 cysteine-rich transmembrane module containing 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1615904 Cystm1 cysteine-rich transmembrane module containing 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20181227 MGI 1615904 Cystm1 cysteine-rich transmembrane module containing 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1615904 Cystm1 cysteine-rich transmembrane module containing 1 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20210128 MGI 1615904 Cystm1 cysteine-rich transmembrane module containing 1 gene MP:0011940 decreased food intake IEA N RGD:5509061 20210128 MGI 1615904 Cystm1 cysteine-rich transmembrane module containing 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1615906 Rogdi rogdi homolog gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0001399 hyperactivity IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0002083 premature death IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0004422 small temporal bone IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0004441 small occipital bone IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0004470 small nasal bone IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0004540 small maxilla IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0004870 small premaxilla IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0009511 distended stomach IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0010004 abnormal paramedian lobule morphology IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0010005 abnormal lobule simplex morphology IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0010096 abnormal incisor color IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0012446 thin hippocampus stratum oriens IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0030262 frontal bossing IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0030265 parietal bossing IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0030544 abnormal enamel development IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615906 Rogdi rogdi homolog gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20240201 MGI PMID:38172607 1615907 Ranbp17 RAN binding protein 17 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20220519 MGI 1615907 Ranbp17 RAN binding protein 17 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1615907 Ranbp17 RAN binding protein 17 gene MP:0001293 anophthalmia IEA N RGD:5509061 20220519 MGI 1615907 Ranbp17 RAN binding protein 17 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1615907 Ranbp17 RAN binding protein 17 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1615908 Cep295nl CEP295 N-terminal like gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220811 MGI 1615909 Slc35b4 solute carrier family 35, member B4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210422 MGI 1615909 Slc35b4 solute carrier family 35, member B4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210422 MGI 1615909 Slc35b4 solute carrier family 35, member B4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1615909 Slc35b4 solute carrier family 35, member B4 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221103 MGI 1615909 Slc35b4 solute carrier family 35, member B4 gene MP:0002833 increased heart weight IEA N RGD:5509061 20231207 MGI 1615909 Slc35b4 solute carrier family 35, member B4 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20221103 MGI 1615909 Slc35b4 solute carrier family 35, member B4 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20221103 MGI 1615909 Slc35b4 solute carrier family 35, member B4 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20221103 MGI 1615909 Slc35b4 solute carrier family 35, member B4 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20221103 MGI 1615909 Slc35b4 solute carrier family 35, member B4 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20221103 MGI 1615909 Slc35b4 solute carrier family 35, member B4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210422 MGI 1615909 Slc35b4 solute carrier family 35, member B4 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 1615910 Gpr180 G protein-coupled receptor 180 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12538434 1615910 Gpr180 G protein-coupled receptor 180 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:12538434 1615911 Nap1l5 nucleosome assembly protein 1-like 5 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20220811 MGI 1615912 Dexi dexamethasone-induced transcript gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200402 MGI PMID:31435002 1615913 Fam181b family with sequence similarity 181, member B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160721 MGI PMID:26407640 1615914 Efcc1 EF hand and coiled-coil domain containing 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240627 MGI 1615914 Efcc1 EF hand and coiled-coil domain containing 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1615914 Efcc1 EF hand and coiled-coil domain containing 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1615916 Srrm3 serine/arginine repetitive matrix 3 gene MP:0000745 tremors IAGP N RGD:5509061 20191212 MGI PMID:30995482 1615916 Srrm3 serine/arginine repetitive matrix 3 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20191212 MGI PMID:30995482 1615916 Srrm3 serine/arginine repetitive matrix 3 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20191212 MGI PMID:30995482 1615916 Srrm3 serine/arginine repetitive matrix 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191212 MGI PMID:30995482 1615916 Srrm3 serine/arginine repetitive matrix 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20191212 MGI PMID:30995482 1615916 Srrm3 serine/arginine repetitive matrix 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20191212 MGI PMID:30995482 1615916 Srrm3 serine/arginine repetitive matrix 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20191212 MGI PMID:30995482 1615916 Srrm3 serine/arginine repetitive matrix 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20191212 MGI PMID:30995482 1615916 Srrm3 serine/arginine repetitive matrix 3 gene MP:0002083 premature death IAGP N RGD:5509061 20191212 MGI PMID:30995482 1615916 Srrm3 serine/arginine repetitive matrix 3 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20191212 MGI PMID:30995482 1615916 Srrm3 serine/arginine repetitive matrix 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20191212 MGI PMID:30995482 1615916 Srrm3 serine/arginine repetitive matrix 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20191212 MGI PMID:30995482 1615917 Zbtb32 zinc finger and BTB domain containing 32 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1615917 Zbtb32 zinc finger and BTB domain containing 32 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15542853 1615917 Zbtb32 zinc finger and BTB domain containing 32 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15542853 1615917 Zbtb32 zinc finger and BTB domain containing 32 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20240523 MGI 1615917 Zbtb32 zinc finger and BTB domain containing 32 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1615917 Zbtb32 zinc finger and BTB domain containing 32 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15542853 1615917 Zbtb32 zinc finger and BTB domain containing 32 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15632058 1615917 Zbtb32 zinc finger and BTB domain containing 32 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220519 MGI 1615917 Zbtb32 zinc finger and BTB domain containing 32 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15542853 1615917 Zbtb32 zinc finger and BTB domain containing 32 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15632058 1615917 Zbtb32 zinc finger and BTB domain containing 32 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22965116 1615917 Zbtb32 zinc finger and BTB domain containing 32 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1615917 Zbtb32 zinc finger and BTB domain containing 32 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220519 MGI 1615918 Irgm2 immunity-related GTPase family M member 2 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20210826 MGI 1615918 Irgm2 immunity-related GTPase family M member 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20200402 MGI 1615918 Irgm2 immunity-related GTPase family M member 2 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20210826 MGI 1615918 Irgm2 immunity-related GTPase family M member 2 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20210826 MGI 1615918 Irgm2 immunity-related GTPase family M member 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1615918 Irgm2 immunity-related GTPase family M member 2 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20211118 MGI PMID:34078740 1615918 Irgm2 immunity-related GTPase family M member 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 1615918 Irgm2 immunity-related GTPase family M member 2 gene MP:0010750 increased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20211118 MGI PMID:34078740 1615918 Irgm2 immunity-related GTPase family M member 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0004917 abnormal T cell selection IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0008353 increased mature gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615919 Sit1 suppression inducing transmembrane adaptor 1 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:16107703 1615922 Gp9 glycoprotein 9 platelet gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 1615922 Gp9 glycoprotein 9 platelet gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1615926 Elovl1 ELOVL fatty acid elongase 1 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:23689133 1615926 Elovl1 ELOVL fatty acid elongase 1 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:23689133 1615926 Elovl1 ELOVL fatty acid elongase 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:23689133 1615926 Elovl1 ELOVL fatty acid elongase 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20180621 MGI PMID:29174370 1615926 Elovl1 ELOVL fatty acid elongase 1 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:23689133 1615926 Elovl1 ELOVL fatty acid elongase 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:23689133 1615926 Elovl1 ELOVL fatty acid elongase 1 gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:23689133 1615926 Elovl1 ELOVL fatty acid elongase 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:23689133 1615926 Elovl1 ELOVL fatty acid elongase 1 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20141003 MGI PMID:23689133 1615926 Elovl1 ELOVL fatty acid elongase 1 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:23689133 1615926 Elovl1 ELOVL fatty acid elongase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23689133 1615926 Elovl1 ELOVL fatty acid elongase 1 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20141003 MGI PMID:23689133 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:12482940 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:12482940 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20200730 MGI PMID:23102608 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20200730 MGI PMID:23102608 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18412165 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18412165 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0002433 abnormal T-helper 1 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15756639 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0002434 abnormal T-helper 2 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15756639 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200730 MGI PMID:23102608 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15756639 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20200730 MGI PMID:23102608 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:12482940 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008073 abnormal CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200730 MGI PMID:23102608 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200730 MGI PMID:23102608 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008091 decreased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:12482940 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:12482940 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12482940 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200730 MGI PMID:23102608 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20141003 MGI PMID:18412165 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:18412165 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20200730 MGI PMID:23102608 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:18412165 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:12482940 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0010065 decreased circulating creatine level IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0011445 abnormal renal protein reabsorption IAGP N RGD:5509061 20141003 MGI PMID:18779924 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200730 MGI PMID:23102608 1615927 Ebi3 Epstein-Barr virus induced gene 3 gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200730 MGI PMID:23102608 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0000111 cleft palate IEA N RGD:5509061 20230601 MGI 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20230601 MGI 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180315 MGI PMID:28784662 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180315 MGI PMID:28784662 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230601 MGI 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20230601 MGI 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230601 MGI 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0001785 edema IEA N RGD:5509061 20230601 MGI 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20230601 MGI 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20230601 MGI 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180315 MGI PMID:28784662 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0009422 decreased gastrocnemius weight IAGP N RGD:5509061 20180315 MGI PMID:28784662 1615929 Hacd1 3-hydroxyacyl-CoA dehydratase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:24493797 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:24493797 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20180215 MGI PMID:27886188 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20180215 MGI PMID:27886188 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:24493797 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:24493797 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20150108 MGI 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20150108 MGI 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0008573 increased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:24493797 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20141003 MGI PMID:24493797 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:24493797 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:24493797 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:24493797 1615930 Usp21 ubiquitin specific peptidase 21 gene MP:0031023 decreased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:24493797 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20240328 MGI PMID:38194265 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20240328 MGI PMID:38194265 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:22393392 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:27168150 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0000746 weakness IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0000774 decreased brain size IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20200310 MGI PMID:21464304 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20200310 MGI PMID:27168150 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20200310 MGI PMID:21464304 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20200310 MGI PMID:24121114 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20200310 MGI PMID:16364897 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:27168150 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20200310 MGI PMID:16242683 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:17956903 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:17956903 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:27168150 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:27168150 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:16242683 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:17956903 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:22393392 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:27168150 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20200310 MGI PMID:17956903 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20200310 MGI PMID:27168150 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20200310 MGI PMID:22393392 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20200310 MGI PMID:16364897 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20200310 MGI PMID:27168150 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001504 abnormal posture IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001505 hunched posture IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001512 trunk curl IAGP N RGD:5509061 20200310 MGI PMID:27168150 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001512 trunk curl IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001513 limb grasping IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20200310 MGI PMID:17956903 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001525 impaired balance IAGP N RGD:5509061 20200310 MGI PMID:16242683 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001525 impaired balance IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0002083 premature death IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:27168150 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0002183 gliosis IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0002183 gliosis IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0002183 gliosis IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20240328 MGI PMID:38194265 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:16364897 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:20457914 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:22393392 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20200310 MGI PMID:26183317 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20200310 MGI PMID:21464304 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20200310 MGI PMID:23748075 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20200310 MGI PMID:26183317 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0005323 dystonia IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0005323 dystonia IAGP N RGD:5509061 20200310 MGI PMID:27168150 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0005323 dystonia IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20200310 MGI PMID:16242683 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20200310 MGI PMID:21464304 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20200310 MGI PMID:27168150 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20200310 MGI PMID:24121114 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0008914 enlarged cerebellum IAGP N RGD:5509061 20200310 MGI PMID:24121114 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20200310 MGI PMID:17956903 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:27168150 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0009979 abnormal cerebellum deep nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17956903 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22393392 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210527 MGI PMID:32202496 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:27168150 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16364897 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22393392 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16242683 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:26370418 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0012267 abnormal red nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0012268 absent red nucleus IAGP N RGD:5509061 20200310 MGI PMID:24937429 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20200310 MGI PMID:16364897 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0020421 increased freezing behavior IAGP N RGD:5509061 20200310 MGI PMID:27168150 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0020560 abnormal pontine nuclei morphology IAGP N RGD:5509061 20200310 MGI PMID:16242683 1615931 Tor1a torsin family 1, member A (torsin A) gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:16242683 1615934 Zfp275 zinc finger protein 275 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20170105 MGI 1615934 Zfp275 zinc finger protein 275 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1615935 Srp9 signal recognition particle 9 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20240523 MGI 1615935 Srp9 signal recognition particle 9 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1615935 Srp9 signal recognition particle 9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1615935 Srp9 signal recognition particle 9 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1615935 Srp9 signal recognition particle 9 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1615935 Srp9 signal recognition particle 9 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1615936 Ncoa4 nuclear receptor coactivator 4 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20150910 MGI PMID:24910095 1615936 Ncoa4 nuclear receptor coactivator 4 gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20150910 MGI PMID:24910095 1615936 Ncoa4 nuclear receptor coactivator 4 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20150910 MGI PMID:24910095 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20211021 MGI 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20221215 MGI 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10561464 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0005505 thrombocytosis IEA N RGD:5509061 20210128 MGI 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20170504 MGI 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20170504 MGI 1615937 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase) gene MP:0030278 thick neurocranium IAGP N RGD:5509061 20171102 MGI PMID:10561464 1615938 Trim24 tripartite motif-containing 24 gene MP:0001573 abnormal circulating alanine transaminase level IAGP N RGD:5509061 20160929 MGI PMID:27534441 1615938 Trim24 tripartite motif-containing 24 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18026104 1615938 Trim24 tripartite motif-containing 24 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18026104 1615938 Trim24 tripartite motif-containing 24 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18026104 1615938 Trim24 tripartite motif-containing 24 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:18026104 1615938 Trim24 tripartite motif-containing 24 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18026104 1615938 Trim24 tripartite motif-containing 24 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240404 MGI PMID:35803934 1615939 Thbs1 thrombospondin 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:12213711 1615939 Thbs1 thrombospondin 1 gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:12584168 1615939 Thbs1 thrombospondin 1 gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:9486968 1615939 Thbs1 thrombospondin 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9486968 1615939 Thbs1 thrombospondin 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9486968 1615939 Thbs1 thrombospondin 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9486968 1615939 Thbs1 thrombospondin 1 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19284971 1615939 Thbs1 thrombospondin 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1615939 Thbs1 thrombospondin 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1615939 Thbs1 thrombospondin 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:12584168 1615939 Thbs1 thrombospondin 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:17293482 1615939 Thbs1 thrombospondin 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20170105 MGI 1615939 Thbs1 thrombospondin 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:12213711 1615939 Thbs1 thrombospondin 1 gene MP:0001204 decreased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:18787106 1615939 Thbs1 thrombospondin 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:12584168 1615939 Thbs1 thrombospondin 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19700744 1615939 Thbs1 thrombospondin 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:19700744 1615939 Thbs1 thrombospondin 1 gene MP:0001348 abnormal lacrimal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:19700744 1615939 Thbs1 thrombospondin 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12584168 1615939 Thbs1 thrombospondin 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12213711 1615939 Thbs1 thrombospondin 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:9486968 1615939 Thbs1 thrombospondin 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:9486968 1615939 Thbs1 thrombospondin 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9486968 1615939 Thbs1 thrombospondin 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12584168 1615939 Thbs1 thrombospondin 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12584168 1615939 Thbs1 thrombospondin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12584168 1615939 Thbs1 thrombospondin 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:12213711 1615939 Thbs1 thrombospondin 1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12584168 1615939 Thbs1 thrombospondin 1 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:12213711 1615939 Thbs1 thrombospondin 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1615939 Thbs1 thrombospondin 1 gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:17293482 1615939 Thbs1 thrombospondin 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12213711 1615939 Thbs1 thrombospondin 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:16294224 1615939 Thbs1 thrombospondin 1 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18787106 1615939 Thbs1 thrombospondin 1 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:19700744 1615939 Thbs1 thrombospondin 1 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19284971 1615939 Thbs1 thrombospondin 1 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19700744 1615939 Thbs1 thrombospondin 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9486968 1615939 Thbs1 thrombospondin 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9486968 1615939 Thbs1 thrombospondin 1 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:19700744 1615939 Thbs1 thrombospondin 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:19284971 1615939 Thbs1 thrombospondin 1 gene MP:0005488 bronchial epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0005489 vascular smooth muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0005490 increased club cell number IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0005492 exocrine pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0005493 stomach epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0005494 esophagogastric junction metaplasia IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:17293482 1615939 Thbs1 thrombospondin 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20201002 MGI PMID:12213711 1615939 Thbs1 thrombospondin 1 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19700744 1615939 Thbs1 thrombospondin 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:17293482 1615939 Thbs1 thrombospondin 1 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19284971 1615939 Thbs1 thrombospondin 1 gene MP:0006266 decreased pulse pressure IAGP N RGD:5509061 20141003 MGI PMID:19284971 1615939 Thbs1 thrombospondin 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19700744 1615939 Thbs1 thrombospondin 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19700744 1615939 Thbs1 thrombospondin 1 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:19700744 1615939 Thbs1 thrombospondin 1 gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:19700744 1615939 Thbs1 thrombospondin 1 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0009343 dilated gallbladder IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0009493 abnormal cystic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0009591 increased liver adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1615939 Thbs1 thrombospondin 1 gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0010909 pulmonary alveolar hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12213711 1615939 Thbs1 thrombospondin 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9486968 1615939 Thbs1 thrombospondin 1 gene MP:0011372 decreased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16294224 1615939 Thbs1 thrombospondin 1 gene MP:0011376 abnormal kidney corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:9657149 1615939 Thbs1 thrombospondin 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11696456 1615939 Thbs1 thrombospondin 1 gene MP:0013452 increased lacrimal gland apoptosis IAGP N RGD:5509061 20150319 MGI PMID:19700744 1615939 Thbs1 thrombospondin 1 gene MP:0013462 abnormal conjunctiva goblet cell number IAGP N RGD:5509061 20150319 MGI PMID:19700744 1615939 Thbs1 thrombospondin 1 gene MP:0013464 decreased conjunctiva goblet cell number IAGP N RGD:5509061 20150319 MGI PMID:19700744 1615941 Tsc22d1 TSC22 domain family, member 1 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20200310 MGI PMID:19329776 1615941 Tsc22d1 TSC22 domain family, member 1 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20200310 MGI PMID:19329776 1615941 Tsc22d1 TSC22 domain family, member 1 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20200310 MGI PMID:19329776 1615944 Hltf helicase-like transcription factor gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:23826137 1615944 Hltf helicase-like transcription factor gene MP:0001257 increased body length IEA N RGD:5509061 20230119 MGI 1615944 Hltf helicase-like transcription factor gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20180125 MGI PMID:22452792 1615944 Hltf helicase-like transcription factor gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:23826137 1615944 Hltf helicase-like transcription factor gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:23415230 1615944 Hltf helicase-like transcription factor gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:23415230 1615944 Hltf helicase-like transcription factor gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20150903 MGI PMID:23826137 1615944 Hltf helicase-like transcription factor gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20180125 MGI PMID:22452792 1615944 Hltf helicase-like transcription factor gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23415230 1615944 Hltf helicase-like transcription factor gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23826137 1615944 Hltf helicase-like transcription factor gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230119 MGI 1615944 Hltf helicase-like transcription factor gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20160428 MGI PMID:23826137 1615945 Slfn4 schlafen 4 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20231012 MGI PMID:37334372 1615945 Slfn4 schlafen 4 gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20231012 MGI PMID:37334372 1615945 Slfn4 schlafen 4 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20231012 MGI PMID:37334372 1615945 Slfn4 schlafen 4 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20231012 MGI PMID:37334372 1615945 Slfn4 schlafen 4 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20231012 MGI PMID:37334372 1615947 Ptprk protein tyrosine phosphatase receptor type K gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1615947 Ptprk protein tyrosine phosphatase receptor type K gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1615947 Ptprk protein tyrosine phosphatase receptor type K gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20240523 MGI 1615947 Ptprk protein tyrosine phosphatase receptor type K gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1615948 Ptprcap protein tyrosine phosphatase receptor type C polypeptide-associated protein gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10602004 1615948 Ptprcap protein tyrosine phosphatase receptor type C polypeptide-associated protein gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10602004 1615948 Ptprcap protein tyrosine phosphatase receptor type C polypeptide-associated protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10602003 1615948 Ptprcap protein tyrosine phosphatase receptor type C polypeptide-associated protein gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9607926 1615948 Ptprcap protein tyrosine phosphatase receptor type C polypeptide-associated protein gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9607926 1615948 Ptprcap protein tyrosine phosphatase receptor type C polypeptide-associated protein gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9607926 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18203137 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:18203137 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21030681 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23509324 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17555992 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15197172 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18203137 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17555992 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21030681 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21030681 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0005089 decreased double-negative T cell number IEA N RGD:5509061 20141003 MGI 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:15197172 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18203137 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:21030681 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23509324 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0008083 decreased single-positive T cell number IEA N RGD:5509061 20111116 MGI 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21030681 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17555992 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21030681 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17555992 1615949 Ptcra pre T cell antigen receptor alpha gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23509324 1615950 Ptch2 patched 2 gene MP:0000172 abnormal bone marrow cell number IEA N RGD:5509061 20200310 MGI 1615950 Ptch2 patched 2 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20200310 MGI 1615950 Ptch2 patched 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20200310 MGI 1615950 Ptch2 patched 2 gene MP:0000240 extramedullary hematopoiesis IEA N RGD:5509061 20200310 MGI 1615950 Ptch2 patched 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20200310 MGI PMID:16914743 1615950 Ptch2 patched 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20200310 MGI PMID:16849540 1615950 Ptch2 patched 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200310 MGI 1615950 Ptch2 patched 2 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20200310 MGI PMID:16914743 1615950 Ptch2 patched 2 gene MP:0001212 skin lesions IAGP N RGD:5509061 20200310 MGI PMID:16914743 1615950 Ptch2 patched 2 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:16914743 1615950 Ptch2 patched 2 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:16914743 1615950 Ptch2 patched 2 gene MP:0001577 anemia IEA N RGD:5509061 20200310 MGI 1615950 Ptch2 patched 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:16849540 1615950 Ptch2 patched 2 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:16849540 1615950 Ptch2 patched 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:16849540 1615950 Ptch2 patched 2 gene MP:0002447 abnormal erythrocyte morphology IEA N RGD:5509061 20200310 MGI 1615950 Ptch2 patched 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20200310 MGI 1615950 Ptch2 patched 2 gene MP:0004175 telangiectasia IAGP N RGD:5509061 20200310 MGI PMID:16849540 1615950 Ptch2 patched 2 gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:16849540 1615950 Ptch2 patched 2 gene MP:0004478 increased testicular teratoma incidence IAGP N RGD:5509061 20200310 MGI PMID:16849540 1615950 Ptch2 patched 2 gene MP:0004971 dermal hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:16914743 1615950 Ptch2 patched 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1615950 Ptch2 patched 2 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20200310 MGI PMID:16849540 1615950 Ptch2 patched 2 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20200310 MGI PMID:16849540 1615950 Ptch2 patched 2 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20200310 MGI 1615950 Ptch2 patched 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1615954 Naip5 NLR family, apoptosis inhibitory protein 5 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:1987055 1615954 Naip5 NLR family, apoptosis inhibitory protein 5 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:18724372 1615954 Naip5 NLR family, apoptosis inhibitory protein 5 gene MP:0012555 decreased cell death IAGP N RGD:5509061 20141003 MGI PMID:18724372 1615957 Naip1 NLR family, apoptosis inhibitory protein 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1615957 Naip1 NLR family, apoptosis inhibitory protein 1 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:10681452 1615958 Myo15a myosin XVA gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:12966030 1615958 Myo15a myosin XVA gene MP:0000043 organ of Corti degeneration IEA N RGD:5509061 20150507 MGI 1615958 Myo15a myosin XVA gene MP:0000048 abnormal stria vascularis morphology IEA N RGD:5509061 20150507 MGI 1615958 Myo15a myosin XVA gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12966030 1615958 Myo15a myosin XVA gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230601 MGI 1615958 Myo15a myosin XVA gene MP:0001304 cataract IEA N RGD:5509061 20230601 MGI 1615958 Myo15a myosin XVA gene MP:0001393 ataxia IEA N RGD:5509061 20180215 MGI 1615958 Myo15a myosin XVA gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0001405 impaired coordination IEA N RGD:5509061 20141003 MGI 1615958 Myo15a myosin XVA gene MP:0001410 head bobbing IEA N RGD:5509061 20111116 MGI 1615958 Myo15a myosin XVA gene MP:0001522 impaired swimming IEA N RGD:5509061 20111116 MGI 1615958 Myo15a myosin XVA gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0001967 deafness IAGP N RGD:5509061 20160929 MGI PMID:27534441 1615958 Myo15a myosin XVA gene MP:0001967 deafness IAGP N RGD:5509061 20180830 MGI PMID:26302205 1615958 Myo15a myosin XVA gene MP:0001967 deafness IAGP N RGD:5509061 20201029 MGI PMID:29985171 1615958 Myo15a myosin XVA gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20111116 MGI 1615958 Myo15a myosin XVA gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20150507 MGI PMID:6889851 1615958 Myo15a myosin XVA gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20180830 MGI PMID:26302205 1615958 Myo15a myosin XVA gene MP:0002730 head shaking IEA N RGD:5509061 20150507 MGI 1615958 Myo15a myosin XVA gene MP:0002855 abnormal cochlear ganglion morphology IEA N RGD:5509061 20150507 MGI 1615958 Myo15a myosin XVA gene MP:0002857 cochlear ganglion degeneration IEA N RGD:5509061 20150507 MGI 1615958 Myo15a myosin XVA gene MP:0003149 abnormal tectorial membrane morphology IEA N RGD:5509061 20150507 MGI 1615958 Myo15a myosin XVA gene MP:0003637 cochlear ganglion hypoplasia IEA N RGD:5509061 20111116 MGI 1615958 Myo15a myosin XVA gene MP:0003879 abnormal hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0004333 abnormal utricular macula morphology IEA N RGD:5509061 20150507 MGI 1615958 Myo15a myosin XVA gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20180830 MGI PMID:26302205 1615958 Myo15a myosin XVA gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20201029 MGI PMID:29985171 1615958 Myo15a myosin XVA gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20332152 1615958 Myo15a myosin XVA gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20201029 MGI PMID:29985171 1615958 Myo15a myosin XVA gene MP:0004405 absent cochlear hair cells IEA N RGD:5509061 20111116 MGI 1615958 Myo15a myosin XVA gene MP:0004413 absent cochlear microphonics IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0004415 abnormal cochlear nerve compound action potential IAGP N RGD:5509061 20201029 MGI PMID:29985171 1615958 Myo15a myosin XVA gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20180830 MGI PMID:26302205 1615958 Myo15a myosin XVA gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20201029 MGI PMID:29985171 1615958 Myo15a myosin XVA gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:12966030 1615958 Myo15a myosin XVA gene MP:0004524 short cochlear hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:12966030 1615958 Myo15a myosin XVA gene MP:0004524 short cochlear hair cell stereocilia IAGP N RGD:5509061 20180830 MGI PMID:26302205 1615958 Myo15a myosin XVA gene MP:0004525 thin cochlear hair cell stereocilia IAGP N RGD:5509061 20180830 MGI PMID:26302205 1615958 Myo15a myosin XVA gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20201029 MGI PMID:29985171 1615958 Myo15a myosin XVA gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0004531 short outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:18160714 1615958 Myo15a myosin XVA gene MP:0004531 short outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:20332152 1615958 Myo15a myosin XVA gene MP:0004531 short outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20180830 MGI PMID:26302205 1615958 Myo15a myosin XVA gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20201029 MGI PMID:29985171 1615958 Myo15a myosin XVA gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0004536 short inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0004536 short inner hair cell stereocilia IAGP N RGD:5509061 20180830 MGI PMID:26302205 1615958 Myo15a myosin XVA gene MP:0004577 abnormal cochlear hair cell inter-stereocilial links morphology IAGP N RGD:5509061 20180830 MGI PMID:26302205 1615958 Myo15a myosin XVA gene MP:0004578 abnormal cochlear hair bundle tip links morphology IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0004716 abnormal cochlear nerve morphology IAGP N RGD:5509061 20201029 MGI PMID:29985171 1615958 Myo15a myosin XVA gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20180830 MGI PMID:26302205 1615958 Myo15a myosin XVA gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20141003 MGI 1615958 Myo15a myosin XVA gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20201029 MGI PMID:29985171 1615958 Myo15a myosin XVA gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0004746 abnormal cochlear IHC afferent innervation pattern IAGP N RGD:5509061 20201029 MGI PMID:29985171 1615958 Myo15a myosin XVA gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12966030 1615958 Myo15a myosin XVA gene MP:0005191 head tilt IEA N RGD:5509061 20141003 MGI 1615958 Myo15a myosin XVA gene MP:0006324 abnormal cochlear nerve fiber response IAGP N RGD:5509061 20201029 MGI PMID:29985171 1615958 Myo15a myosin XVA gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0006335 abnormal hearing electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20230601 MGI 1615958 Myo15a myosin XVA gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20201029 MGI PMID:29985171 1615958 Myo15a myosin XVA gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1615958 Myo15a myosin XVA gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1615958 Myo15a myosin XVA gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21436032 1615958 Myo15a myosin XVA gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20180830 MGI PMID:26302205 1615958 Myo15a myosin XVA gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20201029 MGI PMID:29985171 1615958 Myo15a myosin XVA gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:29985171 1615958 Myo15a myosin XVA gene MP:0020359 abnormal ribbon synapse morphology IAGP N RGD:5509061 20201029 MGI PMID:29985171 1615958 Myo15a myosin XVA gene MP:0030950 abnormal synaptic vesicle exocytosis IAGP N RGD:5509061 20201029 MGI PMID:29985171 1615959 Mylpf myosin light chain, phosphorylatable, fast skeletal muscle gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17356007 1615959 Mylpf myosin light chain, phosphorylatable, fast skeletal muscle gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17356007 1615959 Mylpf myosin light chain, phosphorylatable, fast skeletal muscle gene MP:0004846 absent skeletal muscle IAGP N RGD:5509061 20141003 MGI PMID:17356007 1615959 Mylpf myosin light chain, phosphorylatable, fast skeletal muscle gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17356007 1615963 Krt6b keratin 6B gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:17851587 1615963 Krt6b keratin 6B gene MP:0000467 abnormal esophagus morphology IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615963 Krt6b keratin 6B gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:15601842 1615963 Krt6b keratin 6B gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:17851587 1615963 Krt6b keratin 6B gene MP:0000763 abnormal filiform papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615963 Krt6b keratin 6B gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615963 Krt6b keratin 6B gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15601842 1615963 Krt6b keratin 6B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615963 Krt6b keratin 6B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615963 Krt6b keratin 6B gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615963 Krt6b keratin 6B gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:15601842 1615963 Krt6b keratin 6B gene MP:0003756 abnormal hard palate morphology IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615963 Krt6b keratin 6B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615963 Krt6b keratin 6B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15601842 1615963 Krt6b keratin 6B gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615964 Krt6a keratin 6A gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:17851587 1615964 Krt6a keratin 6A gene MP:0000467 abnormal esophagus morphology IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615964 Krt6a keratin 6A gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:15601842 1615964 Krt6a keratin 6A gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:17851587 1615964 Krt6a keratin 6A gene MP:0000763 abnormal filiform papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615964 Krt6a keratin 6A gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615964 Krt6a keratin 6A gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15601842 1615964 Krt6a keratin 6A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615964 Krt6a keratin 6A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615964 Krt6a keratin 6A gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615964 Krt6a keratin 6A gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:10866680 1615964 Krt6a keratin 6A gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:15601842 1615964 Krt6a keratin 6A gene MP:0003756 abnormal hard palate morphology IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615964 Krt6a keratin 6A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615964 Krt6a keratin 6A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15601842 1615964 Krt6a keratin 6A gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:10953016 1615966 Krt31 keratin 31 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201022 MGI 1615967 Sspn sarcospan gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210520 MGI 1615967 Sspn sarcospan gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0002608 increased hematocrit IEA N RGD:5509061 20211021 MGI 1615967 Sspn sarcospan gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22734004 1615967 Sspn sarcospan gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0010225 abnormal quadriceps morphology IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0010226 increased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:22798625 1615967 Sspn sarcospan gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:22798625 1615970 Klra8 killer cell lectin-like receptor, subfamily A, member 8 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15784573 1615970 Klra8 killer cell lectin-like receptor, subfamily A, member 8 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15784573 1615970 Klra8 killer cell lectin-like receptor, subfamily A, member 8 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15784573 1615970 Klra8 killer cell lectin-like receptor, subfamily A, member 8 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15784573 1615970 Klra8 killer cell lectin-like receptor, subfamily A, member 8 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:15784573 1615970 Klra8 killer cell lectin-like receptor, subfamily A, member 8 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:15784573 1615970 Klra8 killer cell lectin-like receptor, subfamily A, member 8 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:15784573 1615970 Klra8 killer cell lectin-like receptor, subfamily A, member 8 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:15784573 1615970 Klra8 killer cell lectin-like receptor, subfamily A, member 8 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15784573 1615970 Klra8 killer cell lectin-like receptor, subfamily A, member 8 gene MP:0008838 decreased transforming growth factor beta level IAGP N RGD:5509061 20141003 MGI PMID:15784573 1615970 Klra8 killer cell lectin-like receptor, subfamily A, member 8 gene MP:0009787 increased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15784573 1615970 Klra8 killer cell lectin-like receptor, subfamily A, member 8 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:11326273 1615970 Klra8 killer cell lectin-like receptor, subfamily A, member 8 gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:11326273 1615970 Klra8 killer cell lectin-like receptor, subfamily A, member 8 gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:7806288 1615980 Klra1 killer cell lectin-like receptor, subfamily A, member 1 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20180913 MGI PMID:28923946 1615980 Klra1 killer cell lectin-like receptor, subfamily A, member 1 gene MP:0011719 abnormal natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20180913 MGI PMID:28923946 1615996 Jpt1 Jupiter microtubule associated homolog 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0000373 belly spot IAGP N RGD:5509061 20181108 MGI PMID:23633513 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20181108 MGI PMID:19343791 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20181108 MGI PMID:19343791 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21263068 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20181108 MGI PMID:23633513 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20181227 MGI 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21263068 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20181108 MGI PMID:19343791 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20181108 MGI PMID:19343791 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20181108 MGI PMID:19343791 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0008912 nervous IAGP N RGD:5509061 20181108 MGI PMID:19343791 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20181108 MGI PMID:19343791 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20181108 MGI PMID:23633513 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0009784 abnormal melanoblast migration IAGP N RGD:5509061 20181108 MGI PMID:23633513 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0010740 abnormal dendritic cell chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:21263068 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0010860 abnormal anterior commissure pars posterior morphology IAGP N RGD:5509061 20181108 MGI PMID:19343791 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20181108 MGI PMID:19343791 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20181108 MGI PMID:23633513 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20181108 MGI PMID:23633513 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20181108 MGI PMID:19343791 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1615998 Fscn1 fascin actin-bundling protein 1 gene MP:0030930 decreased digit pigmentation IAGP N RGD:5509061 20190117 MGI PMID:23633513 1616001 Evi5 ecotropic viral integration site 5 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1616003 Etv6 ets variant 6 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1616003 Etv6 ets variant 6 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1616003 Etv6 ets variant 6 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210128 MGI 1616003 Etv6 ets variant 6 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15371326 1616003 Etv6 ets variant 6 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:15371326 1616003 Etv6 ets variant 6 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:15371326 1616003 Etv6 ets variant 6 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1616003 Etv6 ets variant 6 gene MP:0000274 enlarged heart IEA N RGD:5509061 20201022 MGI 1616003 Etv6 ets variant 6 gene MP:0000277 abnormal heart shape IEA N RGD:5509061 20210520 MGI 1616003 Etv6 ets variant 6 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:9250681 1616003 Etv6 ets variant 6 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20201022 MGI 1616003 Etv6 ets variant 6 gene MP:0000601 small liver IEA N RGD:5509061 20201022 MGI 1616003 Etv6 ets variant 6 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:9250681 1616003 Etv6 ets variant 6 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:15371326 1616003 Etv6 ets variant 6 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:9250681 1616003 Etv6 ets variant 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0001884 mammary gland alveolar hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18068631 1616003 Etv6 ets variant 6 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21628403 1616003 Etv6 ets variant 6 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18068631 1616003 Etv6 ets variant 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21628403 1616003 Etv6 ets variant 6 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15371326 1616003 Etv6 ets variant 6 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20240111 MGI PMID:37522715 1616003 Etv6 ets variant 6 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1616003 Etv6 ets variant 6 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:15371326 1616003 Etv6 ets variant 6 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0003405 abnormal platelet shape IAGP N RGD:5509061 20240111 MGI PMID:37522715 1616003 Etv6 ets variant 6 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20210520 MGI 1616003 Etv6 ets variant 6 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9250681 1616003 Etv6 ets variant 6 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0004857 abnormal heart weight IEA N RGD:5509061 20211021 MGI 1616003 Etv6 ets variant 6 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1616003 Etv6 ets variant 6 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1616003 Etv6 ets variant 6 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1616003 Etv6 ets variant 6 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:18068631 1616003 Etv6 ets variant 6 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 1616003 Etv6 ets variant 6 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20240111 MGI PMID:37522715 1616003 Etv6 ets variant 6 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0008725 increased heart atrium size IEA N RGD:5509061 20210520 MGI 1616003 Etv6 ets variant 6 gene MP:0008821 increased blood uric acid level IEA N RGD:5509061 20210128 MGI 1616003 Etv6 ets variant 6 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18068631 1616003 Etv6 ets variant 6 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20150402 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15371326 1616003 Etv6 ets variant 6 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21628403 1616003 Etv6 ets variant 6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9250681 1616003 Etv6 ets variant 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616003 Etv6 ets variant 6 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15371326 1616003 Etv6 ets variant 6 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19570513 1616003 Etv6 ets variant 6 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21628403 1616003 Etv6 ets variant 6 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 1616003 Etv6 ets variant 6 gene MP:0013693 abnormal hemopoiesis IAGP N RGD:5509061 20240111 MGI PMID:37522715 1616003 Etv6 ets variant 6 gene MP:0013707 abnormal hematopoietic precursor cell morphology IAGP N RGD:5509061 20240111 MGI PMID:37522715 1616003 Etv6 ets variant 6 gene MP:0020215 impaired blood coagulation IAGP N RGD:5509061 20240111 MGI PMID:37522715 1616004 Etv2 ets variant 2 gene MP:0000215 absent erythrocytes IAGP N RGD:5509061 20200310 MGI PMID:22570122 1616004 Etv2 ets variant 2 gene MP:0000216 absent erythroid progenitor cell IAGP N RGD:5509061 20200310 MGI PMID:22570122 1616004 Etv2 ets variant 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:21425416 1616004 Etv2 ets variant 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20200310 MGI PMID:19129488 1616004 Etv2 ets variant 2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20200310 MGI PMID:23335233 1616004 Etv2 ets variant 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20200310 MGI PMID:19129488 1616004 Etv2 ets variant 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20200310 MGI PMID:21425416 1616004 Etv2 ets variant 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:21425416 1616004 Etv2 ets variant 2 gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20200310 MGI PMID:21425416 1616004 Etv2 ets variant 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:18462699 1616004 Etv2 ets variant 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:18462699 1616004 Etv2 ets variant 2 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20200310 MGI PMID:18462699 1616004 Etv2 ets variant 2 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20200310 MGI PMID:18462699 1616004 Etv2 ets variant 2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20200310 MGI PMID:18462699 1616004 Etv2 ets variant 2 gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20200310 MGI PMID:18462699 1616004 Etv2 ets variant 2 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20200310 MGI PMID:18462699 1616004 Etv2 ets variant 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:19129488 1616004 Etv2 ets variant 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:21425416 1616004 Etv2 ets variant 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:22570122 1616004 Etv2 ets variant 2 gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20200310 MGI PMID:21425416 1616004 Etv2 ets variant 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:23335233 1616004 Etv2 ets variant 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:18462699 1616004 Etv2 ets variant 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:19129488 1616004 Etv2 ets variant 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:22570122 1616004 Etv2 ets variant 2 gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20200310 MGI PMID:19129488 1616004 Etv2 ets variant 2 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20200310 MGI PMID:18462699 1616004 Etv2 ets variant 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20200310 MGI PMID:19129488 1616004 Etv2 ets variant 2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20200310 MGI PMID:21425416 1616004 Etv2 ets variant 2 gene MP:0006057 decreased vascular endothelial cell number IAGP N RGD:5509061 20200310 MGI PMID:23335233 1616004 Etv2 ets variant 2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:18462699 1616004 Etv2 ets variant 2 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20200310 MGI PMID:21425416 1616004 Etv2 ets variant 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18462699 1616004 Etv2 ets variant 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19129488 1616004 Etv2 ets variant 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22570122 1616004 Etv2 ets variant 2 gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20200310 MGI PMID:23335233 1616004 Etv2 ets variant 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:18462699 1616005 Cnn2 calponin 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18617524 1616005 Cnn2 calponin 2 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18617524 1616005 Cnn2 calponin 2 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:18617524 1616005 Cnn2 calponin 2 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18617524 1616005 Cnn2 calponin 2 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18617524 1616005 Cnn2 calponin 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18617524 1616005 Cnn2 calponin 2 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:18617524 1616005 Cnn2 calponin 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18617524 1616005 Cnn2 calponin 2 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:18617524 1616006 Clgn calmegin gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:12376108 1616006 Clgn calmegin gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9177349 1616006 Clgn calmegin gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20200102 MGI PMID:9177349 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:21068328 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15876356 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:20220021 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:20220021 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:21068328 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:15876356 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15876356 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15876356 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21068328 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15876356 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21068328 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15876356 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21068328 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20220021 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21068328 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15876356 1616011 Adam22 a disintegrin and metallopeptidase domain 22 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21068328 1616012 Acta2 actin alpha 2, smooth muscle, aorta gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11053242 1616012 Acta2 actin alpha 2, smooth muscle, aorta gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:11053242 1616012 Acta2 actin alpha 2, smooth muscle, aorta gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:11053242 1616012 Acta2 actin alpha 2, smooth muscle, aorta gene MP:0002834 decreased heart weight IEA N RGD:5509061 20230119 MGI 1616012 Acta2 actin alpha 2, smooth muscle, aorta gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:11053242 1616012 Acta2 actin alpha 2, smooth muscle, aorta gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:16723488 1616012 Acta2 actin alpha 2, smooth muscle, aorta gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16723488 1616012 Acta2 actin alpha 2, smooth muscle, aorta gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16723488 1616012 Acta2 actin alpha 2, smooth muscle, aorta gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11053242 1616012 Acta2 actin alpha 2, smooth muscle, aorta gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11053242 1616050 Hottip Hoxa distal transcript antisense RNA gene MP:0000747 muscle weakness IAGP N RGD:5509061 20161229 MGI PMID:25909911 1616050 Hottip Hoxa distal transcript antisense RNA gene MP:0001513 limb grasping IAGP N RGD:5509061 20161229 MGI PMID:25909911 1616050 Hottip Hoxa distal transcript antisense RNA gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24381249 1616050 Hottip Hoxa distal transcript antisense RNA gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20161229 MGI PMID:25909911 1616050 Hottip Hoxa distal transcript antisense RNA gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20161229 MGI PMID:25909911 1616050 Hottip Hoxa distal transcript antisense RNA gene MP:0009422 decreased gastrocnemius weight IAGP N RGD:5509061 20161229 MGI PMID:25909911 1616050 Hottip Hoxa distal transcript antisense RNA gene MP:0009728 abnormal calcaneum morphology IAGP N RGD:5509061 20161229 MGI PMID:25909911 1616050 Hottip Hoxa distal transcript antisense RNA gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20161229 MGI PMID:25909911 1616102 Duxf5 double homeobox family member 5 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20231026 MGI PMID:31591446 1616112 Cd99 CD99 antigen gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22350746 1616183 Zfp541 zinc finger protein 541 gene MP:0001147 small testis IAGP N RGD:5509061 20230817 MGI PMID:35341968 1616183 Zfp541 zinc finger protein 541 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20230817 MGI PMID:35341968 1616183 Zfp541 zinc finger protein 541 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20230817 MGI PMID:35341968 1616183 Zfp541 zinc finger protein 541 gene MP:0001925 male infertility IAGP N RGD:5509061 20210930 MGI PMID:33961623 1616183 Zfp541 zinc finger protein 541 gene MP:0001925 male infertility IAGP N RGD:5509061 20230817 MGI PMID:35341968 1616183 Zfp541 zinc finger protein 541 gene MP:0005159 azoospermia IAGP N RGD:5509061 20230817 MGI PMID:35341968 1616183 Zfp541 zinc finger protein 541 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20210930 MGI PMID:33961623 1616183 Zfp541 zinc finger protein 541 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20230817 MGI PMID:35341968 1616183 Zfp541 zinc finger protein 541 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1616183 Zfp541 zinc finger protein 541 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20230817 MGI PMID:35341968 1616183 Zfp541 zinc finger protein 541 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210930 MGI PMID:33961623 1616183 Zfp541 zinc finger protein 541 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20210930 MGI PMID:33961623 1616183 Zfp541 zinc finger protein 541 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20230817 MGI PMID:35341968 1616183 Zfp541 zinc finger protein 541 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20210930 MGI PMID:33961623 1616183 Zfp541 zinc finger protein 541 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1616183 Zfp541 zinc finger protein 541 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20230817 MGI PMID:35341968 1616183 Zfp541 zinc finger protein 541 gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20210930 MGI PMID:33961623 1616183 Zfp541 zinc finger protein 541 gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20230817 MGI PMID:35341968 1616183 Zfp541 zinc finger protein 541 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20230817 MGI PMID:35341968 1616183 Zfp541 zinc finger protein 541 gene MP:0030935 increased primordial germ cell apoptosis IAGP N RGD:5509061 20210930 MGI PMID:33961623 1616197 Tmem249 transmembrane protein 249 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20231026 MGI PMID:36993167 1616197 Tmem249 transmembrane protein 249 gene MP:0001925 male infertility IAGP N RGD:5509061 20231026 MGI PMID:36993167 1616197 Tmem249 transmembrane protein 249 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20231026 MGI PMID:36993167 1616197 Tmem249 transmembrane protein 249 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20231026 MGI PMID:36993167 1616197 Tmem249 transmembrane protein 249 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20231026 MGI PMID:36993167 1616197 Tmem249 transmembrane protein 249 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20231026 MGI PMID:36993167 1616197 Tmem249 transmembrane protein 249 gene MP:0009279 abnormal activated sperm motility IAGP N RGD:5509061 20231026 MGI PMID:36993167 1616197 Tmem249 transmembrane protein 249 gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20231026 MGI PMID:36993167 1616197 Tmem249 transmembrane protein 249 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20231026 MGI PMID:36993167 1616210 Plb1 phospholipase B1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20220519 MGI 1616210 Plb1 phospholipase B1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1616210 Plb1 phospholipase B1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220811 MGI 1616210 Plb1 phospholipase B1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1616240 Angptl7 angiopoietin-like 7 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20210610 MGI PMID:25652910 1616240 Angptl7 angiopoietin-like 7 gene MP:0011246 abnormal fetal liver hematopoietic progenitor cell morphology IAGP N RGD:5509061 20210610 MGI PMID:25652910 1616240 Angptl7 angiopoietin-like 7 gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20210610 MGI PMID:25652910 1616244 Sptbn5 spectrin beta, non-erythrocytic 5 gene MP:0004716 abnormal cochlear nerve morphology IAGP N RGD:5509061 20240307 MGI PMID:35864018 1616244 Sptbn5 spectrin beta, non-erythrocytic 5 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20240307 MGI PMID:35864018 1616248 Vmn2r53 vomeronasal 2, receptor 53 gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20220922 MGI PMID:35654036 1616248 Vmn2r53 vomeronasal 2, receptor 53 gene MP:0021115 abnormal aggression towards conspecific IAGP N RGD:5509061 20220922 MGI PMID:35654036 1616266 Otogl otogelin-like gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20210520 MGI 1616266 Otogl otogelin-like gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1616266 Otogl otogelin-like gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1616266 Otogl otogelin-like gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20181227 MGI 1616266 Otogl otogelin-like gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20200402 MGI 1616266 Otogl otogelin-like gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20200402 MGI 1616266 Otogl otogelin-like gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1616266 Otogl otogelin-like gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1616288 H2ab3 H2A.B variant histone 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20190627 MGI PMID:30704500 1616288 H2ab3 H2A.B variant histone 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20190627 MGI PMID:30704500 1616288 H2ab3 H2A.B variant histone 3 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20190627 MGI PMID:30704500 1616288 H2ab3 H2A.B variant histone 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20190627 MGI PMID:30704500 1616288 H2ab3 H2A.B variant histone 3 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1616288 H2ab3 H2A.B variant histone 3 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 1616288 H2ab3 H2A.B variant histone 3 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20190627 MGI PMID:30704500 1616288 H2ab3 H2A.B variant histone 3 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20190627 MGI PMID:30704500 1616288 H2ab3 H2A.B variant histone 3 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20190627 MGI PMID:30704500 1616291 Rgs21 regulator of G-protein signalling 21 gene MP:0001985 abnormal gustatory system physiology IAGP N RGD:5509061 20191003 MGI PMID:29701767 1616291 Rgs21 regulator of G-protein signalling 21 gene MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20191003 MGI PMID:29701767 1616291 Rgs21 regulator of G-protein signalling 21 gene MP:0004209 abnormal sweet taste sensitivity IAGP N RGD:5509061 20191003 MGI PMID:29701767 1616291 Rgs21 regulator of G-protein signalling 21 gene MP:0004210 abnormal bitter taste sensitivity IAGP N RGD:5509061 20191003 MGI PMID:29701767 1616291 Rgs21 regulator of G-protein signalling 21 gene MP:0004212 abnormal salty taste sensitivity IAGP N RGD:5509061 20191003 MGI PMID:29701767 1616291 Rgs21 regulator of G-protein signalling 21 gene MP:0004213 abnormal umami taste sensitivity IAGP N RGD:5509061 20191003 MGI PMID:29701767 1616295 Lipt1 lipoyltransferase 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1616295 Lipt1 lipoyltransferase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200917 MGI PMID:31042466 1616295 Lipt1 lipoyltransferase 1 gene MP:0003717 pallor IAGP N RGD:5509061 20200917 MGI PMID:31042466 1616295 Lipt1 lipoyltransferase 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1616295 Lipt1 lipoyltransferase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200917 MGI PMID:31042466 1616295 Lipt1 lipoyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616309 Nhsl2 NHS like 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1616309 Nhsl2 NHS like 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1616309 Nhsl2 NHS like 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1616309 Nhsl2 NHS like 2 gene MP:0001200 thick skin IEA N RGD:5509061 20210128 MGI 1616309 Nhsl2 NHS like 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1616309 Nhsl2 NHS like 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1616309 Nhsl2 NHS like 2 gene MP:0002637 small uterus IEA N RGD:5509061 20210128 MGI 1616309 Nhsl2 NHS like 2 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210128 MGI 1616315 Vmn2r117 vomeronasal 2, receptor 117 gene MP:0002243 abnormal vomeronasal organ morphology IAGP N RGD:5509061 20210225 MGI PMID:30367054 1616331 Acp4 acid phosphatase 4 gene MP:0002576 abnormal enamel morphology IEA N RGD:5509061 20210617 MGI 1616345 Pramel17 PRAME like 17 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1616345 Pramel17 PRAME like 17 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20210128 MGI 1616345 Pramel17 PRAME like 17 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20231207 MGI 1616345 Pramel17 PRAME like 17 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 1616349 Clec4a4 C-type lectin domain family 4, member a4 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1616349 Clec4a4 C-type lectin domain family 4, member a4 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1616350 Gpr31b G protein-coupled receptor 31, D17Leh66b region gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20191003 MGI PMID:30675063 1616350 Gpr31b G protein-coupled receptor 31, D17Leh66b region gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20191003 MGI PMID:30675063 1616350 Gpr31b G protein-coupled receptor 31, D17Leh66b region gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20191003 MGI PMID:30675063 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20160929 MGI PMID:27534441 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:13336002 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:12405956 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:15347914 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0001409 increased stereotypic behavior IEA N RGD:5509061 20111116 MGI 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:15347914 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20210826 MGI 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220519 MGI 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0001522 impaired swimming IEA N RGD:5509061 20111116 MGI 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0001961 abnormal reflex IEA N RGD:5509061 20111116 MGI 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11276175 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:13336002 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15347914 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0001967 deafness IAGP N RGD:5509061 20160929 MGI PMID:27534441 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20221215 MGI 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:13336002 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:13336002 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:13336002 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:13336002 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12405956 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004331 vestibular saccular macula degeneration IAGP N RGD:5509061 20141003 MGI PMID:13336002 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12405956 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:13336002 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20141003 MGI PMID:13336002 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11276175 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15347914 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:12405956 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004428 abnormal type I vestibular cell IAGP N RGD:5509061 20141003 MGI PMID:11276175 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004428 abnormal type I vestibular cell IAGP N RGD:5509061 20141003 MGI PMID:15347914 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:12405956 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004519 thin vestibular hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:12405956 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:12405956 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004525 thin cochlear hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:12405956 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15347914 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:11276175 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15347914 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:11276175 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004536 short inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:11276175 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004536 short inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:20137774 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004578 abnormal cochlear hair bundle tip links morphology IAGP N RGD:5509061 20141003 MGI PMID:11276175 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220519 MGI 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:20137774 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:12405956 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:20137774 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15347914 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220519 MGI 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0011063 absent inner hair cell kinocilia IAGP N RGD:5509061 20141003 MGI PMID:11276175 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11276175 1616352 Grxcr1 glutaredoxin, cysteine rich 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15347914 1616357 Nom1 nucleolar protein with MIF4G domain 1 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20190124 MGI PMID:25340873 1616367 Garin3 golgi associated RAB2 interactor 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20240801 MGI PMID:38935810 1616367 Garin3 golgi associated RAB2 interactor 3 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240801 MGI PMID:38935810 1616367 Garin3 golgi associated RAB2 interactor 3 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20240801 MGI PMID:38935810 1616367 Garin3 golgi associated RAB2 interactor 3 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240801 MGI PMID:38935810 1616367 Garin3 golgi associated RAB2 interactor 3 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20240801 MGI PMID:38935810 1616367 Garin3 golgi associated RAB2 interactor 3 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20240801 MGI PMID:38935810 1616371 Tmem204 transmembrane protein 204 gene MP:0010196 abnormal lymphatic vessel smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:20439428 1616371 Tmem204 transmembrane protein 204 gene MP:0010200 enlarged lymphatic vessel IAGP N RGD:5509061 20141003 MGI PMID:20439428 1616372 Baz2b bromodomain adjacent to zinc finger domain, 2B gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1616372 Baz2b bromodomain adjacent to zinc finger domain, 2B gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1616372 Baz2b bromodomain adjacent to zinc finger domain, 2B gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1616372 Baz2b bromodomain adjacent to zinc finger domain, 2B gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200402 MGI 1616372 Baz2b bromodomain adjacent to zinc finger domain, 2B gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20220721 MGI PMID:35090595 1616372 Baz2b bromodomain adjacent to zinc finger domain, 2B gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1616372 Baz2b bromodomain adjacent to zinc finger domain, 2B gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20200402 MGI 1616372 Baz2b bromodomain adjacent to zinc finger domain, 2B gene MP:0005516 enhanced liver regeneration IAGP N RGD:5509061 20220721 MGI PMID:35090595 1616372 Baz2b bromodomain adjacent to zinc finger domain, 2B gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20200402 MGI 1616372 Baz2b bromodomain adjacent to zinc finger domain, 2B gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20220721 MGI PMID:35090595 1616372 Baz2b bromodomain adjacent to zinc finger domain, 2B gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 1616372 Baz2b bromodomain adjacent to zinc finger domain, 2B gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1616373 Znrf3 zinc and ring finger 3 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22895187 1616373 Znrf3 zinc and ring finger 3 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:22575959 1616373 Znrf3 zinc and ring finger 3 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:22575959 1616373 Znrf3 zinc and ring finger 3 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22895187 1616373 Znrf3 zinc and ring finger 3 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22895187 1616373 Znrf3 zinc and ring finger 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22575959 1616373 Znrf3 zinc and ring finger 3 gene MP:0012168 abnormal optic placode morphology IAGP N RGD:5509061 20141003 MGI PMID:22575959 1616373 Znrf3 zinc and ring finger 3 gene MP:0013485 increased Paneth cell number IAGP N RGD:5509061 20150312 MGI PMID:22895187 1616374 BC031181 cDNA sequence BC031181 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1616375 Timd6 T cell immunoglobulin and mucin domain containing 6 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 1616375 Timd6 T cell immunoglobulin and mucin domain containing 6 gene MP:0001512 trunk curl IEA N RGD:5509061 20231207 MGI 1616375 Timd6 T cell immunoglobulin and mucin domain containing 6 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20231207 MGI 1616375 Timd6 T cell immunoglobulin and mucin domain containing 6 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 1616375 Timd6 T cell immunoglobulin and mucin domain containing 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1616378 Flrt1 fibronectin leucine rich transmembrane protein 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170406 MGI 1616396 Ceacam23 CEA cell adhesion moleculen23 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230720 MGI 1616398 Sbk2 SH3-binding domain kinase family, member 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210520 MGI 1616403 Apold1 apolipoprotein L domain containing 1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20210401 MGI PMID:22681709 1616405 Cracr2a calcium release activated channel regulator 2A gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20210805 MGI PMID:27016526 1616405 Cracr2a calcium release activated channel regulator 2A gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20210805 MGI PMID:27016526 1616408 Tatdn2 TatD DNase domain containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616408 Tatdn2 TatD DNase domain containing 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1616408 Tatdn2 TatD DNase domain containing 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20210826 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210520 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210826 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20210826 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20210826 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20220519 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20210826 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1616410 Sfmbt2 Scm-like with four mbt domains 2 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1616411 Pcdhac2 protocadherin alpha subfamily C, 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17572674 1616412 Pcdhac1 protocadherin alpha subfamily C, 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17572674 1616414 Pcdha2 protocadherin alpha 2 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1616414 Pcdha2 protocadherin alpha 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1616414 Pcdha2 protocadherin alpha 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20200310 MGI PMID:21931569 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200310 MGI PMID:12955145 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200310 MGI PMID:21931569 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0000445 short snout IAGP N RGD:5509061 20200310 MGI PMID:21507892 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0000445 short snout IAGP N RGD:5509061 20200310 MGI PMID:21931569 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20200310 MGI PMID:21507892 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20200310 MGI PMID:23221805 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20200310 MGI PMID:23536828 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20200310 MGI PMID:16880404 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20200310 MGI PMID:22613833 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20200310 MGI PMID:22613833 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20200310 MGI PMID:6793660 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20200310 MGI PMID:15345741 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20200310 MGI PMID:16880404 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0001208 blistering IAGP N RGD:5509061 20200310 MGI PMID:16880404 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0001208 blistering IAGP N RGD:5509061 20200310 MGI PMID:6793660 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:6793660 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20200310 MGI PMID:15345741 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200310 MGI PMID:6793660 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:12955145 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:23221805 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:23536828 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20200310 MGI PMID:6793660 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0001310 abnormal conjunctiva morphology IAGP N RGD:5509061 20200310 MGI PMID:21507892 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20200310 MGI PMID:21507892 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0001341 absent eyelids IAGP N RGD:5509061 20200310 MGI PMID:15345741 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0002089 abnormal postnatal growth/weight/body size IEA N RGD:5509061 20200310 MGI 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200310 MGI PMID:15345741 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200310 MGI PMID:23221805 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20200310 MGI PMID:15345741 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:15345741 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:6793660 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:22613833 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20200310 MGI PMID:21931569 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0003153 early eyelid opening IEA N RGD:5509061 20200310 MGI 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20200310 MGI PMID:15345741 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20200310 MGI PMID:23221805 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20200310 MGI PMID:23536828 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0003842 abnormal metopic suture morphology IAGP N RGD:5509061 20200310 MGI PMID:21931569 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20200310 MGI PMID:23221805 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0004472 broad nasal bone IAGP N RGD:5509061 20200310 MGI PMID:21931569 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0005084 abnormal gallbladder morphology IAGP N RGD:5509061 20200310 MGI PMID:23221805 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0005176 eyelids fail to open IEA N RGD:5509061 20200310 MGI 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20200310 MGI PMID:23536828 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0005242 cryptophthalmos IAGP N RGD:5509061 20200310 MGI PMID:15345741 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0005242 cryptophthalmos IAGP N RGD:5509061 20200310 MGI PMID:16880404 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0005242 cryptophthalmos IAGP N RGD:5509061 20200310 MGI PMID:21507892 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0005242 cryptophthalmos IAGP N RGD:5509061 20200310 MGI PMID:23221805 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0005242 cryptophthalmos IAGP N RGD:5509061 20200310 MGI PMID:23536828 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0005262 coloboma IAGP N RGD:5509061 20200310 MGI PMID:21507892 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20200310 MGI PMID:21507892 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0008854 bleb IAGP N RGD:5509061 20200310 MGI PMID:15345741 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0008862 asymmetric snout IAGP N RGD:5509061 20200310 MGI PMID:21931569 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0010977 fused right lung lobes IAGP N RGD:5509061 20200310 MGI PMID:23536828 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20200310 MGI 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23221805 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:21507892 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:21931569 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20200310 MGI PMID:23221805 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0014051 abnormal maxillary-premaxillary suture morphology IAGP N RGD:5509061 20200310 MGI PMID:21931569 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0020856 absent cornea epithelium IAGP N RGD:5509061 20200310 MGI PMID:21507892 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:6793660 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20200310 MGI PMID:21931569 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0030166 increased inner canthal distance IAGP N RGD:5509061 20200310 MGI PMID:21507892 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0030193 short philtrum IAGP N RGD:5509061 20200310 MGI PMID:21507892 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0030195 abnormal internasal suture morphology IAGP N RGD:5509061 20200310 MGI PMID:21931569 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0030367 premature metopic suture closure IAGP N RGD:5509061 20200310 MGI PMID:21931569 1616422 Frem1 Fras1 related extracellular matrix protein 1 gene MP:0030368 trigonocephaly IAGP N RGD:5509061 20200310 MGI PMID:21931569 1616424 Cimip2b ciliary microtubule inner protein 2B gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20231207 MGI 1616424 Cimip2b ciliary microtubule inner protein 2B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 1616424 Cimip2b ciliary microtubule inner protein 2B gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20231207 MGI 1616424 Cimip2b ciliary microtubule inner protein 2B gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20200310 MGI PMID:11919684 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20230831 MGI PMID:34004180 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:11919684 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:15353999 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:17701983 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20230713 MGI PMID:29615807 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20230720 MGI PMID:21875659 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000445 short snout IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000446 long snout IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000486 abnormal pulmonary trunk morphology IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000547 short limbs IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000706 small thymus IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20230622 MGI PMID:29168327 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20230713 MGI PMID:19279158 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20230727 MGI PMID:24368733 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20230713 MGI PMID:19279158 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20230622 MGI PMID:29168327 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000794 abnormal parietal lobe morphology IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000798 abnormal frontal lobe morphology IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20230713 MGI PMID:28317875 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20230622 MGI PMID:29168327 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20230713 MGI PMID:28317875 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20230622 MGI PMID:29168327 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20230727 MGI PMID:24368733 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20230622 MGI PMID:29168327 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20230713 MGI PMID:28317875 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000865 absent cerebellum vermis IAGP N RGD:5509061 20230727 MGI PMID:24368733 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20230713 MGI PMID:28317875 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20230720 MGI PMID:36288662 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20231130 MGI PMID:30108144 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001127 small ovary IAGP N RGD:5509061 20220721 MGI PMID:35402599 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220721 MGI PMID:35402599 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001258 decreased body length IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230713 MGI PMID:29615807 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:11919684 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230209 MGI PMID:29311329 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20200310 MGI PMID:26670829 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001304 cataract IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001306 small lens IAGP N RGD:5509061 20200310 MGI PMID:26670829 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001317 abnormal pupil morphology IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001337 dry eyes IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20200310 MGI PMID:15353999 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:10932191 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:11919684 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:15353999 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:15916118 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:24293546 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001394 circling IAGP N RGD:5509061 20230209 MGI PMID:29311329 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001394 circling IAGP N RGD:5509061 20230713 MGI PMID:29615807 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20200310 MGI PMID:17701983 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:15916118 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001410 head bobbing IAGP N RGD:5509061 20200310 MGI PMID:15353999 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001410 head bobbing IAGP N RGD:5509061 20200310 MGI PMID:15916118 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001410 head bobbing IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001410 head bobbing IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001410 head bobbing IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001410 head bobbing IAGP N RGD:5509061 20200310 MGI PMID:24293546 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001410 head bobbing IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001410 head bobbing IAGP N RGD:5509061 20230713 MGI PMID:29615807 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001512 trunk curl IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20200310 MGI PMID:15353999 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20200310 MGI PMID:15353999 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20200310 MGI PMID:15353999 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20200310 MGI PMID:15353999 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001657 abnormal induced morbidity/mortality IAGP N RGD:5509061 20230720 MGI PMID:21875659 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:24293546 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001785 edema IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20230713 MGI PMID:29615807 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220721 MGI PMID:35402599 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002083 premature death IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20230727 MGI PMID:35129866 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002236 abnormal internal nares morphology IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:17701983 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20230713 MGI PMID:29615807 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20230727 MGI PMID:29467333 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20230706 MGI PMID:15916118 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200310 MGI PMID:24293546 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002683 delayed fertility IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002730 head shaking IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:11919684 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:17701983 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002859 abnormal inner ear canal fusion IAGP N RGD:5509061 20200310 MGI PMID:11919684 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:15916118 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003126 abnormal external female genitalia morphology IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20200310 MGI PMID:15916118 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20230831 MGI PMID:34004180 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20200310 MGI PMID:15916118 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20200310 MGI PMID:17701983 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003162 decreased lateral semicircular canal size IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20200310 MGI PMID:17701983 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003164 decreased posterior semicircular canal size IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003164 decreased posterior semicircular canal size IAGP N RGD:5509061 20230713 MGI PMID:29615807 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003165 absent superior semicircular canal IAGP N RGD:5509061 20230831 MGI PMID:34004180 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003166 decreased superior semicircular canal size IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003166 decreased superior semicircular canal size IAGP N RGD:5509061 20230713 MGI PMID:29615807 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20230713 MGI PMID:28317875 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20230720 MGI PMID:25183173 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:24293546 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20230831 MGI PMID:34732824 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20230831 MGI PMID:34004180 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003330 abnormal auditory tube morphology IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003387 aorta coarctation IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003395 abnormal subclavian artery morphology IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20230713 MGI PMID:28317875 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20230720 MGI PMID:36288662 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20230831 MGI PMID:34004180 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20230831 MGI PMID:34732824 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20200310 MGI PMID:17701983 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20200310 MGI PMID:26670829 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004290 abnormal stapes footplate morphology IAGP N RGD:5509061 20200310 MGI PMID:15353999 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004290 abnormal stapes footplate morphology IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004290 abnormal stapes footplate morphology IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004290 abnormal stapes footplate morphology IAGP N RGD:5509061 20230713 MGI PMID:29615807 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004290 abnormal stapes footplate morphology IAGP N RGD:5509061 20230720 MGI PMID:21875659 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004315 absent vestibular saccule IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004369 absent utricle IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20200310 MGI PMID:15916118 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20230831 MGI PMID:34732824 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20200310 MGI PMID:15353999 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20200310 MGI PMID:15916118 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20230720 MGI PMID:21875659 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20230831 MGI PMID:34004180 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20230831 MGI PMID:34732824 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004407 increased cochlear hair cell number IAGP N RGD:5509061 20230831 MGI PMID:34004180 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004409 abnormal crista ampullaris neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:17701983 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004413 absent cochlear microphonics IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20200310 MGI PMID:11919684 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004479 abnormal oval window morphology IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004480 abnormal round window morphology IAGP N RGD:5509061 20200310 MGI PMID:15353999 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004480 abnormal round window morphology IAGP N RGD:5509061 20200310 MGI PMID:15916118 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004540 small maxilla IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004568 fusion of glossopharyngeal and vagus nerve IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004592 small mandible IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20200310 MGI 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004718 abnormal vestibular nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:17701983 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20230720 MGI PMID:21875659 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20230713 MGI PMID:19279158 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220721 MGI PMID:35402599 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004897 otosclerosis IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004922 abnormal common crus morphology IAGP N RGD:5509061 20200310 MGI PMID:17701983 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20200310 MGI 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004925 decreased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20230720 MGI PMID:21875659 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004979 abnormal neuronal precursor cell number IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20230720 MGI PMID:25183173 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20230720 MGI PMID:25183173 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20200310 MGI PMID:11919684 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20200310 MGI PMID:11919684 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20200310 MGI PMID:15353999 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20200310 MGI PMID:15916118 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20230720 MGI PMID:21875659 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005191 head tilt IAGP N RGD:5509061 20230713 MGI PMID:29615807 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005251 blepharitis IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005251 blepharitis IAGP N RGD:5509061 20230713 MGI PMID:29615807 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005262 coloboma IAGP N RGD:5509061 20200310 MGI PMID:26670829 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005307 head tossing IAGP N RGD:5509061 20200310 MGI PMID:11919684 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20200310 MGI PMID:26670829 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005628 decreased circulating potassium level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0005652 sex reversal IAGP N RGD:5509061 20230209 MGI PMID:29311329 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20230713 MGI PMID:19279158 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006167 eyelid edema IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006292 abnormal nasal placode morphology IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006305 abnormal optic eminence morphology IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006306 abnormal nasal pit morphology IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20230720 MGI PMID:21875659 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006326 conductive hearing impairment IAGP N RGD:5509061 20230720 MGI PMID:21875659 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006329 sensorineural hearing impairment IAGP N RGD:5509061 20230720 MGI PMID:21875659 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006357 abnormal circulating mineral level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008066 small endolymphatic duct IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008374 abnormal malleus manubrium morphology IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20230831 MGI PMID:34732824 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20230629 MGI PMID:36343670 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20230713 MGI PMID:19279158 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20230713 MGI PMID:19279158 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20230713 MGI PMID:26928066 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20230713 MGI PMID:30108144 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20230713 MGI PMID:28317875 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008946 abnormal neuron number IAGP N RGD:5509061 20230720 MGI PMID:25183173 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20230720 MGI PMID:25183173 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20230720 MGI PMID:25183173 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0008970 choanal atresia IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009008 delayed estrous cycle IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009085 abnormal uterine horn morphology IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009101 clitoris hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009229 abnormal neurohypophysis median eminence morphology IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009229 abnormal neurohypophysis median eminence morphology IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20230622 MGI PMID:29168327 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20230713 MGI PMID:26928066 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20221201 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009944 abnormal olfactory lobe morphology IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009957 abnormal cerebellum vermis lobule morphology IAGP N RGD:5509061 20230622 MGI PMID:29168327 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009957 abnormal cerebellum vermis lobule morphology IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009959 abnormal cerebellar hemisphere morphology IAGP N RGD:5509061 20230622 MGI PMID:29168327 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009959 abnormal cerebellar hemisphere morphology IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009963 abnormal cerebellum hemisphere lobule morphology IAGP N RGD:5509061 20230622 MGI PMID:29168327 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009991 abnormal cerebellum vermis lobule IV morphology IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009992 abnormal cerebellum vermis lobule IX morphology IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009993 abnormal cerebellum vermis lobule V morphology IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0009996 abnormal cerebellum vermis lobule VIII morphology IAGP N RGD:5509061 20230622 MGI PMID:29168327 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010005 abnormal lobule simplex morphology IAGP N RGD:5509061 20230622 MGI PMID:29168327 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20230720 MGI PMID:36288662 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010059 olfactory bulb hypoplasia IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010059 olfactory bulb hypoplasia IAGP N RGD:5509061 20230713 MGI PMID:19279158 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010068 decreased red blood cell distribution width IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010165 abnormal response to stress-induced hyperthermia IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010205 abnormal oligodendrocyte apoptosis IAGP N RGD:5509061 20230713 MGI PMID:30108144 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010330 abnormal circulating lipoprotein level IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010433 double inlet heart left ventricle IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010453 abnormal coronary vein morphology IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010455 aortopulmonary window IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010458 pulmonary trunk hypoplasia IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010526 aortic arch coarctation IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010715 retina coloboma IAGP N RGD:5509061 20230209 MGI PMID:29311329 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0010973 increased periosteum thickness IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20230209 MGI PMID:29311329 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20736290 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20230713 MGI PMID:28317875 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24293546 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20230629 MGI PMID:19809474 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20230209 MGI PMID:29311329 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22658483 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220721 MGI PMID:35402599 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220721 MGI PMID:35402599 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220721 MGI PMID:35402599 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011281 abnormal olfactory epithelium cilium morphology IAGP N RGD:5509061 20230713 MGI PMID:19279158 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:24293546 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20230713 MGI PMID:29615807 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20230713 MGI PMID:26102480 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20230713 MGI PMID:19279158 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20230713 MGI PMID:26928066 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011861 increased cranium height IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20230713 MGI PMID:29615807 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20230720 MGI PMID:21875659 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20230720 MGI PMID:36288662 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20230831 MGI PMID:34732824 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0012020 abnormal olfactory epithelium physiology IAGP N RGD:5509061 20230713 MGI PMID:19279158 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20200310 MGI PMID:24293546 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20230720 MGI PMID:25183173 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0012206 increased neuronal stem cell self-renewal IAGP N RGD:5509061 20230720 MGI PMID:25183173 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0012451 abnormal retrosplenial granular cortex morphology IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0012455 increased mammillothalamic tract size IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0012462 decreased brain internal capsule size IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0012481 increased habenula size IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0012535 abnormal optic fissure closure IAGP N RGD:5509061 20230209 MGI PMID:29311329 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0012756 impaired cranial neural crest cell differentiation IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0012757 abnormal cranial neural crest cell migration IAGP N RGD:5509061 20210121 MGI PMID:33127760 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0013350 Rathke's pouch hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:17334657 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20230713 MGI PMID:26928066 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0013466 keratoconjunctivitis sicca IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20220721 MGI PMID:35402599 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0013551 decreased cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0013616 decreased volumetric bone mineral density IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0013767 decreased palatal rugae number IAGP N RGD:5509061 20200310 MGI PMID:16207732 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0013820 absent optic cup IAGP N RGD:5509061 20200310 MGI PMID:26670829 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0014333 short retina cone cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:36343670 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:36343670 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0014490 abnormal inner ear vestibular sensory neuron innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:17701983 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0020348 decreased olfactory sensory neuron number IAGP N RGD:5509061 20230713 MGI PMID:19279158 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0020900 abnormal middle ear epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0020903 increased middle ear goblet cell number IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0021165 behavioral developmental delay IAGP N RGD:5509061 20230713 MGI PMID:28165338 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0030009 increased bone marrow adipose tissue amount IAGP N RGD:5509061 20230629 MGI PMID:35418650 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0030060 absent nasal pit IAGP N RGD:5509061 20230713 MGI PMID:21596839 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0030099 facial asymmetry IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0030109 abnormal incudomalleolar joint morphology IAGP N RGD:5509061 20200310 MGI PMID:11919684 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0030127 small stapes IAGP N RGD:5509061 20230713 MGI PMID:29615807 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0030340 absent fourth pharyngeal arch artery IAGP N RGD:5509061 20200310 MGI PMID:19855134 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0030394 abnormal incus short process morphology IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0030396 abnormal incus long process morphology IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0030402 abnormal stapes head morphology IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0030405 small stapes obturator foramen IAGP N RGD:5509061 20200310 MGI PMID:22539951 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0030407 abnormal stapes crus morpholgy IAGP N RGD:5509061 20200310 MGI PMID:11919684 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0030411 decreased round window size IAGP N RGD:5509061 20230720 MGI PMID:21875659 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0030831 abnormal glenoid fossa morphology IAGP N RGD:5509061 20200310 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:24293546 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220721 MGI PMID:35402599 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220721 MGI PMID:35402599 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:24840056 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20230706 MGI PMID:36232804 1616427 Chd7 chromodomain helicase DNA binding protein 7 gene MP:0031491 decreased oval window size IAGP N RGD:5509061 20230810 MGI PMID:21875659 1616437 Ipo8 importin 8 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1616437 Ipo8 importin 8 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1616437 Ipo8 importin 8 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1616437 Ipo8 importin 8 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20240523 MGI 1616437 Ipo8 importin 8 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1616437 Ipo8 importin 8 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1616439 Abi3bp ABI family member 3 binding protein gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20211014 MGI PMID:25296984 1616439 Abi3bp ABI family member 3 binding protein gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230601 MGI 1616439 Abi3bp ABI family member 3 binding protein gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20231207 MGI 1616439 Abi3bp ABI family member 3 binding protein gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20200310 MGI PMID:27521794 1616439 Abi3bp ABI family member 3 binding protein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1616439 Abi3bp ABI family member 3 binding protein gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20211014 MGI PMID:25296984 1616439 Abi3bp ABI family member 3 binding protein gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 1616439 Abi3bp ABI family member 3 binding protein gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1616439 Abi3bp ABI family member 3 binding protein gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1616439 Abi3bp ABI family member 3 binding protein gene MP:0031217 increased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20211014 MGI PMID:25296984 1616439 Abi3bp ABI family member 3 binding protein gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:25296984 1616440 Tmem117 transmembrane protein 117 gene MP:0002710 increased glucagon secretion IAGP N RGD:5509061 20240404 MGI PMID:37314252 1616440 Tmem117 transmembrane protein 117 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20240404 MGI PMID:37314252 1616440 Tmem117 transmembrane protein 117 gene MP:0005610 increased circulating antidiuretic hormone level IAGP N RGD:5509061 20240404 MGI PMID:37314252 1616440 Tmem117 transmembrane protein 117 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20240404 MGI PMID:37314252 1616440 Tmem117 transmembrane protein 117 gene MP:0020879 abnormal calcium level IAGP N RGD:5509061 20240404 MGI PMID:37314252 1616442 Tafa4 TAFA chemokine like family member 4 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20191114 MGI PMID:24139797 1616442 Tafa4 TAFA chemokine like family member 4 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20231207 MGI 1616442 Tafa4 TAFA chemokine like family member 4 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20191114 MGI PMID:24139797 1616442 Tafa4 TAFA chemokine like family member 4 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20191114 MGI PMID:24139797 1616442 Tafa4 TAFA chemokine like family member 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1616442 Tafa4 TAFA chemokine like family member 4 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20191114 MGI PMID:24139797 1616442 Tafa4 TAFA chemokine like family member 4 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20191114 MGI PMID:24139797 1616444 Insyn1 inhibitory synaptic factor 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20201022 MGI PMID:31829939 1616444 Insyn1 inhibitory synaptic factor 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20201022 MGI PMID:31829939 1616444 Insyn1 inhibitory synaptic factor 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20201022 MGI PMID:31829939 1616444 Insyn1 inhibitory synaptic factor 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20201022 MGI PMID:31829939 1616444 Insyn1 inhibitory synaptic factor 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20201022 MGI PMID:31829939 1616444 Insyn1 inhibitory synaptic factor 1 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20201022 MGI PMID:31829939 1616444 Insyn1 inhibitory synaptic factor 1 gene MP:0012006 abnormal hippocampus physiology IAGP N RGD:5509061 20201022 MGI PMID:31829939 1616444 Insyn1 inhibitory synaptic factor 1 gene MP:0020358 abnormal inhibitory synapse morphology IAGP N RGD:5509061 20201022 MGI PMID:31829939 1616447 Pld5 phospholipase D family member 5 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210520 MGI 1616447 Pld5 phospholipase D family member 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160915 MGI PMID:24652767 1616447 Pld5 phospholipase D family member 5 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210520 MGI 1616447 Pld5 phospholipase D family member 5 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20200402 MGI 1616447 Pld5 phospholipase D family member 5 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210520 MGI 1616447 Pld5 phospholipase D family member 5 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20210520 MGI 1616450 C5ar2 complement component 5a receptor 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230119 MGI 1616450 C5ar2 complement component 5a receptor 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:19620784 1616450 C5ar2 complement component 5a receptor 2 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:19620784 1616450 C5ar2 complement component 5a receptor 2 gene MP:0001657 abnormal induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19620784 1616450 C5ar2 complement component 5a receptor 2 gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16204243 1616450 C5ar2 complement component 5a receptor 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16204243 1616450 C5ar2 complement component 5a receptor 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17641279 1616450 C5ar2 complement component 5a receptor 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17641279 1616450 C5ar2 complement component 5a receptor 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19620784 1616450 C5ar2 complement component 5a receptor 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19620784 1616450 C5ar2 complement component 5a receptor 2 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20230119 MGI 1616450 C5ar2 complement component 5a receptor 2 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:19620784 1616450 C5ar2 complement component 5a receptor 2 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:17641279 1616450 C5ar2 complement component 5a receptor 2 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17641279 1616450 C5ar2 complement component 5a receptor 2 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:17641279 1616450 C5ar2 complement component 5a receptor 2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:17641279 1616450 C5ar2 complement component 5a receptor 2 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:17641279 1616451 Hs3st5 heparan sulfate (glucosamine) 3-O-sulfotransferase 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1616451 Hs3st5 heparan sulfate (glucosamine) 3-O-sulfotransferase 5 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1616451 Hs3st5 heparan sulfate (glucosamine) 3-O-sulfotransferase 5 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1616451 Hs3st5 heparan sulfate (glucosamine) 3-O-sulfotransferase 5 gene MP:0002989 small kidney IEA N RGD:5509061 20210128 MGI 1616454 Kif19a kinesin family member 19A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23168168 1616454 Kif19a kinesin family member 19A gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23168168 1616454 Kif19a kinesin family member 19A gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:23168168 1616454 Kif19a kinesin family member 19A gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23168168 1616454 Kif19a kinesin family member 19A gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20141003 MGI PMID:23168168 1616454 Kif19a kinesin family member 19A gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:23168168 1616454 Kif19a kinesin family member 19A gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:23168168 1616454 Kif19a kinesin family member 19A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23168168 1616454 Kif19a kinesin family member 19A gene MP:0011644 abnormal oviduct epithelium motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:23168168 1616454 Kif19a kinesin family member 19A gene MP:0030965 increased brain ependyma motile cilium length IAGP N RGD:5509061 20190725 MGI PMID:23168168 1616457 Slc15a5 solute carrier family 15, member 5 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20230119 MGI 1616460 Esyt3 extended synaptotagmin-like protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170518 MGI PMID:25486202 1616460 Esyt3 extended synaptotagmin-like protein 3 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 1616460 Esyt3 extended synaptotagmin-like protein 3 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20240627 MGI 1616460 Esyt3 extended synaptotagmin-like protein 3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1616460 Esyt3 extended synaptotagmin-like protein 3 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20170518 MGI PMID:25486202 1616460 Esyt3 extended synaptotagmin-like protein 3 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20170518 MGI PMID:25486202 1616460 Esyt3 extended synaptotagmin-like protein 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170518 MGI PMID:25486202 1616460 Esyt3 extended synaptotagmin-like protein 3 gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20170518 MGI PMID:25486202 1616463 Vat1l vesicle amine transport protein 1 like gene MP:0004924 abnormal behavior IEA N RGD:5509061 20141003 MGI 1616464 Lrrc36 leucine rich repeat containing 36 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1616465 Lpcat2 lysophosphatidylcholine acyltransferase 2 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20220811 MGI 1616465 Lpcat2 lysophosphatidylcholine acyltransferase 2 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1616465 Lpcat2 lysophosphatidylcholine acyltransferase 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240627 MGI 1616465 Lpcat2 lysophosphatidylcholine acyltransferase 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1616465 Lpcat2 lysophosphatidylcholine acyltransferase 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1616466 Slc35e1 solute carrier family 35, member E1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20240516 MGI PMID:37296095 1616466 Slc35e1 solute carrier family 35, member E1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240516 MGI PMID:37296095 1616466 Slc35e1 solute carrier family 35, member E1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20240516 MGI PMID:37296095 1616466 Slc35e1 solute carrier family 35, member E1 gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20240516 MGI PMID:37296095 1616466 Slc35e1 solute carrier family 35, member E1 gene MP:0020893 abnormal zinc level IAGP N RGD:5509061 20240516 MGI PMID:37296095 1616467 Map1s microtubule-associated protein 1S gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:21262964 1616467 Map1s microtubule-associated protein 1S gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20200310 MGI PMID:21262964 1616467 Map1s microtubule-associated protein 1S gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:21262964 1616467 Map1s microtubule-associated protein 1S gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20200310 MGI PMID:21262964 1616470 Nalf1 NALCN channel auxiliary factor 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20230601 MGI 1616470 Nalf1 NALCN channel auxiliary factor 1 gene MP:0004357 long tibia IEA N RGD:5509061 20230601 MGI 1616470 Nalf1 NALCN channel auxiliary factor 1 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20230601 MGI 1616470 Nalf1 NALCN channel auxiliary factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1616472 Mtmr12 myotubularin related protein 12 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240627 MGI 1616472 Mtmr12 myotubularin related protein 12 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1616472 Mtmr12 myotubularin related protein 12 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210826 MGI 1616473 Agxt2 alanine-glyoxylate aminotransferase 2 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:23023372 1616473 Agxt2 alanine-glyoxylate aminotransferase 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230119 MGI 1616473 Agxt2 alanine-glyoxylate aminotransferase 2 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:23023372 1616473 Agxt2 alanine-glyoxylate aminotransferase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1616473 Agxt2 alanine-glyoxylate aminotransferase 2 gene MP:0020836 increased circulating citrulline level IAGP N RGD:5509061 20180712 MGI PMID:23023372 1616474 Carmil3 capping protein regulator and myosin 1 linker 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1616474 Carmil3 capping protein regulator and myosin 1 linker 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1616474 Carmil3 capping protein regulator and myosin 1 linker 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1616474 Carmil3 capping protein regulator and myosin 1 linker 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1616474 Carmil3 capping protein regulator and myosin 1 linker 3 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1616476 Acsf2 acyl-CoA synthetase family member 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1616476 Acsf2 acyl-CoA synthetase family member 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1616476 Acsf2 acyl-CoA synthetase family member 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1616476 Acsf2 acyl-CoA synthetase family member 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160421 MGI 1616476 Acsf2 acyl-CoA synthetase family member 2 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20211021 MGI 1616489 Or2l13b olfactory receptor family 2 subfamily L member 13B gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20220609 MGI PMID:35324479 1616489 Or2l13b olfactory receptor family 2 subfamily L member 13B gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20220609 MGI PMID:35324479 1616489 Or2l13b olfactory receptor family 2 subfamily L member 13B gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20220609 MGI PMID:35324479 1616489 Or2l13b olfactory receptor family 2 subfamily L member 13B gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20220609 MGI PMID:35324479 1616507 Tmem255a transmembrane protein 255A gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1616510 Zfp300 zinc finger protein 300 gene MP:0003394 increased cardiac output IEA N RGD:5509061 20220519 MGI 1616510 Zfp300 zinc finger protein 300 gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20220811 MGI 1616511 Gm4984 predicted pseudogene 4984 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240627 MGI PMID:38835510 1616513 Agbl1 ATP/GTP binding protein-like 1 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 1616513 Agbl1 ATP/GTP binding protein-like 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1616513 Agbl1 ATP/GTP binding protein-like 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1616513 Agbl1 ATP/GTP binding protein-like 1 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1616513 Agbl1 ATP/GTP binding protein-like 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1616513 Agbl1 ATP/GTP binding protein-like 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1616513 Agbl1 ATP/GTP binding protein-like 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:18386809 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200123 MGI PMID:31704914 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18386809 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:18386809 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18386809 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18386809 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:18386809 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200123 MGI PMID:31704914 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0002764 short tibia IEA N RGD:5509061 20160421 MGI 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210128 MGI 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0002879 increased cellular sensitivity to X-ray irradiation IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220519 MGI 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:18386809 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160421 MGI 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20220811 MGI 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0005426 tachypnea IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0008404 increased cellular sensitivity to methylmethanesulfonate IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0008570 lipidosis IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:18386809 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:18386809 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18386809 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20160421 MGI 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0009082 uterus cyst IAGP N RGD:5509061 20141003 MGI PMID:18386809 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18386809 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20160421 MGI 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0010138 arteritis IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0010894 pulmonary alveolar edema IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0010909 pulmonary alveolar hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18386809 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16810678 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200123 MGI PMID:31704914 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18386809 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18386809 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19137022 1616514 Chd2 chromodomain helicase DNA binding protein 2 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:18386809 1616516 Klhl21 kelch-like 21 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1616518 Pramel12 PRAME like 12 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1616518 Pramel12 PRAME like 12 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20220519 MGI 1616518 Pramel12 PRAME like 12 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20220519 MGI 1616518 Pramel12 PRAME like 12 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 1616518 Pramel12 PRAME like 12 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1616518 Pramel12 PRAME like 12 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1616518 Pramel12 PRAME like 12 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1616518 Pramel12 PRAME like 12 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1616518 Pramel12 PRAME like 12 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1616518 Pramel12 PRAME like 12 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210520 MGI 1616518 Pramel12 PRAME like 12 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1616518 Pramel12 PRAME like 12 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1616518 Pramel12 PRAME like 12 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1616518 Pramel12 PRAME like 12 gene MP:0002188 small heart IEA N RGD:5509061 20210128 MGI 1616518 Pramel12 PRAME like 12 gene MP:0002989 small kidney IEA N RGD:5509061 20210128 MGI 1616518 Pramel12 PRAME like 12 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20221215 MGI 1616518 Pramel12 PRAME like 12 gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20220519 MGI 1616518 Pramel12 PRAME like 12 gene MP:0004002 abnormal jejunum morphology IEA N RGD:5509061 20220519 MGI 1616520 E2f2 E2F transcription factor 2 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:11511364 1616520 E2f2 E2F transcription factor 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18594513 1616520 E2f2 E2F transcription factor 2 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18594513 1616520 E2f2 E2F transcription factor 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:17608565 1616520 E2f2 E2F transcription factor 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18594513 1616520 E2f2 E2F transcription factor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18594513 1616520 E2f2 E2F transcription factor 2 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11511364 1616520 E2f2 E2F transcription factor 2 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17608565 1616520 E2f2 E2F transcription factor 2 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:17608565 1616520 E2f2 E2F transcription factor 2 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20141003 MGI PMID:17608565 1616520 E2f2 E2F transcription factor 2 gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:11754817 1616520 E2f2 E2F transcription factor 2 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:11754817 1616521 Ifnlr1 interferon lambda receptor 1 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:18250457 1616521 Ifnlr1 interferon lambda receptor 1 gene MP:0002418 increased susceptibility to viral infection IAGP N RGD:5509061 20210527 MGI PMID:31462571 1616521 Ifnlr1 interferon lambda receptor 1 gene MP:0013406 abnormal epidermal immune compartment IEA N RGD:5509061 20201231 MGI 1616521 Ifnlr1 interferon lambda receptor 1 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20210527 MGI PMID:31462571 1616521 Ifnlr1 interferon lambda receptor 1 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20210527 MGI PMID:31462571 1616522 Pde11a phosphodiesterase 11A gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1616522 Pde11a phosphodiesterase 11A gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210520 MGI 1616522 Pde11a phosphodiesterase 11A gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1616522 Pde11a phosphodiesterase 11A gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1616522 Pde11a phosphodiesterase 11A gene MP:0001297 microphthalmia IEA N RGD:5509061 20210128 MGI 1616522 Pde11a phosphodiesterase 11A gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:20404172 1616522 Pde11a phosphodiesterase 11A gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1616522 Pde11a phosphodiesterase 11A gene MP:0002574 increased vertical activity IEA N RGD:5509061 20240523 MGI 1616522 Pde11a phosphodiesterase 11A gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:20404172 1616522 Pde11a phosphodiesterase 11A gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1616522 Pde11a phosphodiesterase 11A gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20404172 1616522 Pde11a phosphodiesterase 11A gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:20404172 1616523 Thada thyroid adenoma associated gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20220519 MGI PMID:35480478 1616524 Lrrc30 leucine rich repeat containing 30 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200514 MGI 1616524 Lrrc30 leucine rich repeat containing 30 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200514 MGI 1616524 Lrrc30 leucine rich repeat containing 30 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20200514 MGI 1616524 Lrrc30 leucine rich repeat containing 30 gene MP:0001589 abnormal mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1616524 Lrrc30 leucine rich repeat containing 30 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20200514 MGI 1616527 Cdc20b cell division cycle 20B gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1616527 Cdc20b cell division cycle 20B gene MP:0002608 increased hematocrit IEA N RGD:5509061 20211021 MGI 1616527 Cdc20b cell division cycle 20B gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1616528 Gapt Grb2-binding adaptor, transmembrane gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:18559951 1616528 Gapt Grb2-binding adaptor, transmembrane gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18559951 1616528 Gapt Grb2-binding adaptor, transmembrane gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18559951 1616528 Gapt Grb2-binding adaptor, transmembrane gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:18559951 1616528 Gapt Grb2-binding adaptor, transmembrane gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:18559951 1616531 Zfp366 zinc finger protein 366 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20150813 MGI 1616531 Zfp366 zinc finger protein 366 gene MP:0000445 short snout IEA N RGD:5509061 20150813 MGI 1616531 Zfp366 zinc finger protein 366 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20150813 MGI 1616531 Zfp366 zinc finger protein 366 gene MP:0000564 syndactyly IEA N RGD:5509061 20150813 MGI 1616531 Zfp366 zinc finger protein 366 gene MP:0001297 microphthalmia IEA N RGD:5509061 20150813 MGI 1616531 Zfp366 zinc finger protein 366 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20150813 MGI 1616531 Zfp366 zinc finger protein 366 gene MP:0002639 micrognathia IEA N RGD:5509061 20150813 MGI 1616531 Zfp366 zinc finger protein 366 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20150813 MGI 1616533 Slc22a29 solute carrier family 22. member 29 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1616533 Slc22a29 solute carrier family 22. member 29 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:16516152 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16516152 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0001261 obese IAGP N RGD:5509061 20171207 MGI PMID:28859131 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0001264 increased body size IEA N RGD:5509061 20180927 MGI 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16516152 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16516152 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16516152 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16516152 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16516152 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20180927 MGI 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:16516152 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20171207 MGI PMID:28859131 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0006325 impaired hearing IEA N RGD:5509061 20141003 MGI 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20171207 MGI PMID:28859131 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20171207 MGI PMID:28859131 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0009255 degranulated pancreatic beta cells IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0009645 crystalluria IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17206865 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:16516152 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20180927 MGI 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:16000322 1616534 Alms1 ALMS1, centrosome and basal body associated gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:28859131 1616536 Cep126 centrosomal protein 126 gene MP:0001925 male infertility IEA N RGD:5509061 20231207 MGI 1616536 Cep126 centrosomal protein 126 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20240523 MGI 1616536 Cep126 centrosomal protein 126 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1616537 Cfap300 cilia and flagella associated protein 300 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1616537 Cfap300 cilia and flagella associated protein 300 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1616539 Dchs1 dachsous cadherin related 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20200310 MGI PMID:26258302 1616539 Dchs1 dachsous cadherin related 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0003641 small lung IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0004321 short sternum IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0006120 mitral valve prolapse IAGP N RGD:5509061 20200310 MGI PMID:26258302 1616539 Dchs1 dachsous cadherin related 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0010614 abnormal mitral valve cusp morphology IAGP N RGD:5509061 20200310 MGI PMID:26258302 1616539 Dchs1 dachsous cadherin related 1 gene MP:0010617 thick mitral valve cusps IAGP N RGD:5509061 20200310 MGI PMID:26258302 1616539 Dchs1 dachsous cadherin related 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616539 Dchs1 dachsous cadherin related 1 gene MP:0012279 wide sternum IAGP N RGD:5509061 20200310 MGI PMID:21303848 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:23940364 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20200310 MGI PMID:23940364 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20200310 MGI PMID:14610273 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20200310 MGI PMID:23940364 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0003620 oliguria IAGP N RGD:5509061 20200310 MGI PMID:20921400 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0004757 abnormal distal convoluted tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:23940364 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20200310 MGI PMID:20921400 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20200310 MGI PMID:23940364 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0005633 increased circulating sodium level IAGP N RGD:5509061 20200310 MGI PMID:21131289 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20200310 MGI PMID:20921400 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20200310 MGI PMID:21131289 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20200310 MGI PMID:23940364 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20200310 MGI PMID:21131289 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:20921400 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20200310 MGI PMID:20921400 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:14610273 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19644017 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0011540 increased urine aldosterone level IAGP N RGD:5509061 20200310 MGI PMID:23940364 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0012339 hyperkalemia IAGP N RGD:5509061 20200310 MGI PMID:23940364 1616541 Wnk1 WNK lysine deficient protein kinase 1 gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20200310 MGI PMID:23940364 1616542 Zfp637 zinc finger protein 637 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20210128 MGI 1616542 Zfp637 zinc finger protein 637 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201022 MGI PMID:32492392 1616542 Zfp637 zinc finger protein 637 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1616543 Gxylt2 glucoside xylosyltransferase 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220811 MGI 1616543 Gxylt2 glucoside xylosyltransferase 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20231207 MGI 1616543 Gxylt2 glucoside xylosyltransferase 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1616544 Dnajc5g DnaJ heat shock protein family (Hsp40) member C5 gamma gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1616544 Dnajc5g DnaJ heat shock protein family (Hsp40) member C5 gamma gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1616544 Dnajc5g DnaJ heat shock protein family (Hsp40) member C5 gamma gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1616544 Dnajc5g DnaJ heat shock protein family (Hsp40) member C5 gamma gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:26829768 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0020928 increased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:26829768 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20220324 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:26829768 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0031034 increased susceptibility to Poxviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:26829768 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0031373 abnormal manchette perinuclear ring morphology IAGP N RGD:5509061 20220407 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0031374 abnormal manchette assembly IAGP N RGD:5509061 20220407 MGI PMID:30635446 1616545 Agbl5 ATP/GTP binding protein-like 5 gene MP:0031375 abnormal manchette disassembly IAGP N RGD:5509061 20220407 MGI PMID:30635446 1616546 Kmt2c lysine (K)-specific methyltransferase 2C gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17021013 1616546 Kmt2c lysine (K)-specific methyltransferase 2C gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210422 MGI PMID:25346535 1616546 Kmt2c lysine (K)-specific methyltransferase 2C gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:17021013 1616546 Kmt2c lysine (K)-specific methyltransferase 2C gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17021013 1616546 Kmt2c lysine (K)-specific methyltransferase 2C gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17021013 1616546 Kmt2c lysine (K)-specific methyltransferase 2C gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17021013 1616546 Kmt2c lysine (K)-specific methyltransferase 2C gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17021013 1616546 Kmt2c lysine (K)-specific methyltransferase 2C gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20210422 MGI PMID:25346535 1616546 Kmt2c lysine (K)-specific methyltransferase 2C gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20210422 MGI PMID:25346535 1616546 Kmt2c lysine (K)-specific methyltransferase 2C gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20210422 MGI PMID:25346535 1616546 Kmt2c lysine (K)-specific methyltransferase 2C gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141016 MGI PMID:24368734 1616546 Kmt2c lysine (K)-specific methyltransferase 2C gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17021013 1616546 Kmt2c lysine (K)-specific methyltransferase 2C gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20210422 MGI PMID:25346535 1616547 Galnt11 polypeptide N-acetylgalactosaminyltransferase 11 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20201210 MGI PMID:31740596 1616547 Galnt11 polypeptide N-acetylgalactosaminyltransferase 11 gene MP:0001265 decreased body size IAGP N RGD:5509061 20201210 MGI PMID:31740596 1616547 Galnt11 polypeptide N-acetylgalactosaminyltransferase 11 gene MP:0002083 premature death IAGP N RGD:5509061 20201210 MGI PMID:31740596 1616547 Galnt11 polypeptide N-acetylgalactosaminyltransferase 11 gene MP:0002871 albuminuria IAGP N RGD:5509061 20201210 MGI PMID:31740596 1616547 Galnt11 polypeptide N-acetylgalactosaminyltransferase 11 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20201210 MGI PMID:31740596 1616547 Galnt11 polypeptide N-acetylgalactosaminyltransferase 11 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20201210 MGI PMID:31740596 1616547 Galnt11 polypeptide N-acetylgalactosaminyltransferase 11 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20201210 MGI PMID:31740596 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:23418536 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:24010020 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:23418536 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:24010020 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:24010020 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23418536 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:24010020 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20160421 MGI 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:24010020 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23418536 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20201022 MGI 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:24010020 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:24010020 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23418536 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160421 MGI 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20181227 MGI 1616549 Gbx1 gastrulation brain homeobox 1 gene MP:0011994 increased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:24010020 1616550 Samd11 sterile alpha motif domain containing 11 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1616550 Samd11 sterile alpha motif domain containing 11 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1616550 Samd11 sterile alpha motif domain containing 11 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1616550 Samd11 sterile alpha motif domain containing 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230907 MGI PMID:33603070 1616550 Samd11 sterile alpha motif domain containing 11 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20230907 MGI PMID:33603070 1616550 Samd11 sterile alpha motif domain containing 11 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20230907 MGI PMID:33603070 1616550 Samd11 sterile alpha motif domain containing 11 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20230907 MGI PMID:33603070 1616550 Samd11 sterile alpha motif domain containing 11 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20230907 MGI PMID:33603070 1616550 Samd11 sterile alpha motif domain containing 11 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20230907 MGI PMID:33603070 1616550 Samd11 sterile alpha motif domain containing 11 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20230907 MGI PMID:33603070 1616550 Samd11 sterile alpha motif domain containing 11 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20230907 MGI PMID:33603070 1616550 Samd11 sterile alpha motif domain containing 11 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20230907 MGI PMID:33603070 1616550 Samd11 sterile alpha motif domain containing 11 gene MP:0012150 increased b-wave implicit time IAGP N RGD:5509061 20230907 MGI PMID:33603070 1616550 Samd11 sterile alpha motif domain containing 11 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210826 MGI 1616551 Plppr4 phospholipid phosphatase related 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19766573 1616551 Plppr4 phospholipid phosphatase related 4 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:19766573 1616551 Plppr4 phospholipid phosphatase related 4 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:19766573 1616551 Plppr4 phospholipid phosphatase related 4 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:19766573 1616551 Plppr4 phospholipid phosphatase related 4 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:19766573 1616551 Plppr4 phospholipid phosphatase related 4 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19766573 1616551 Plppr4 phospholipid phosphatase related 4 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19766573 1616551 Plppr4 phospholipid phosphatase related 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19766573 1616551 Plppr4 phospholipid phosphatase related 4 gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:19766573 1616551 Plppr4 phospholipid phosphatase related 4 gene MP:0014375 increased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:19766573 1616555 Rbm15 RNA binding motif protein 15 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19542301 1616555 Rbm15 RNA binding motif protein 15 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19542301 1616555 Rbm15 RNA binding motif protein 15 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:19542301 1616555 Rbm15 RNA binding motif protein 15 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20150122 MGI PMID:19287095 1616555 Rbm15 RNA binding motif protein 15 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20150122 MGI PMID:19287095 1616555 Rbm15 RNA binding motif protein 15 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19542301 1616555 Rbm15 RNA binding motif protein 15 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17376872 1616555 Rbm15 RNA binding motif protein 15 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19542301 1616555 Rbm15 RNA binding motif protein 15 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:17376872 1616555 Rbm15 RNA binding motif protein 15 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19542301 1616555 Rbm15 RNA binding motif protein 15 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20150122 MGI PMID:19287095 1616555 Rbm15 RNA binding motif protein 15 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19542301 1616555 Rbm15 RNA binding motif protein 15 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17376872 1616555 Rbm15 RNA binding motif protein 15 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20150122 MGI PMID:19287095 1616555 Rbm15 RNA binding motif protein 15 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:17376872 1616555 Rbm15 RNA binding motif protein 15 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17376872 1616555 Rbm15 RNA binding motif protein 15 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19542301 1616555 Rbm15 RNA binding motif protein 15 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17376872 1616555 Rbm15 RNA binding motif protein 15 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:19542301 1616555 Rbm15 RNA binding motif protein 15 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17376872 1616556 Ano3 anoctamin 3 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20211118 MGI PMID:33972431 1616556 Ano3 anoctamin 3 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20221215 MGI 1616556 Ano3 anoctamin 3 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20211118 MGI PMID:33972431 1616557 Ino80d INO80 complex subunit D gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20201022 MGI 1616557 Ino80d INO80 complex subunit D gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1616557 Ino80d INO80 complex subunit D gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1616557 Ino80d INO80 complex subunit D gene MP:0003960 increased lean body mass IEA N RGD:5509061 20190502 MGI 1616557 Ino80d INO80 complex subunit D gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1616557 Ino80d INO80 complex subunit D gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20190502 MGI 1616557 Ino80d INO80 complex subunit D gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1616557 Ino80d INO80 complex subunit D gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1616558 Plcl1 phospholipase C-like 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20150108 MGI PMID:24591640 1616558 Plcl1 phospholipase C-like 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:11867528 1616558 Plcl1 phospholipase C-like 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20150108 MGI PMID:24591640 1616558 Plcl1 phospholipase C-like 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15464766 1616558 Plcl1 phospholipase C-like 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11867528 1616558 Plcl1 phospholipase C-like 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:15464766 1616558 Plcl1 phospholipase C-like 1 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20150108 MGI PMID:24591640 1616558 Plcl1 phospholipase C-like 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20150108 MGI PMID:24591640 1616558 Plcl1 phospholipase C-like 1 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11867528 1616558 Plcl1 phospholipase C-like 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15464766 1616558 Plcl1 phospholipase C-like 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20150108 MGI PMID:24591640 1616560 Ormdl1 ORM1-like 1 (S. cerevisiae) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240627 MGI PMID:37316542 1616560 Ormdl1 ORM1-like 1 (S. cerevisiae) gene MP:0001265 decreased body size IAGP N RGD:5509061 20240627 MGI PMID:37316542 1616560 Ormdl1 ORM1-like 1 (S. cerevisiae) gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20240627 MGI PMID:37316542 1616560 Ormdl1 ORM1-like 1 (S. cerevisiae) gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240627 MGI PMID:37316542 1616560 Ormdl1 ORM1-like 1 (S. cerevisiae) gene MP:0020116 increased sphingosine level IAGP N RGD:5509061 20240627 MGI PMID:37316542 1616560 Ormdl1 ORM1-like 1 (S. cerevisiae) gene MP:0020582 increased ceramide level IAGP N RGD:5509061 20240627 MGI PMID:37316542 1616561 Kdm2a lysine (K)-specific demethylase 2A gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20151217 MGI PMID:25463925 1616561 Kdm2a lysine (K)-specific demethylase 2A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20151217 MGI PMID:25463925 1616561 Kdm2a lysine (K)-specific demethylase 2A gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20151217 MGI PMID:25463925 1616561 Kdm2a lysine (K)-specific demethylase 2A gene MP:0002188 small heart IAGP N RGD:5509061 20151217 MGI PMID:25463925 1616561 Kdm2a lysine (K)-specific demethylase 2A gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20151217 MGI PMID:25463925 1616561 Kdm2a lysine (K)-specific demethylase 2A gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20151217 MGI PMID:25463925 1616561 Kdm2a lysine (K)-specific demethylase 2A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20151217 MGI PMID:25463925 1616561 Kdm2a lysine (K)-specific demethylase 2A gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20151217 MGI PMID:25463925 1616561 Kdm2a lysine (K)-specific demethylase 2A gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20151217 MGI PMID:25463925 1616561 Kdm2a lysine (K)-specific demethylase 2A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20151217 MGI PMID:25463925 1616561 Kdm2a lysine (K)-specific demethylase 2A gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20151217 MGI PMID:25463925 1616561 Kdm2a lysine (K)-specific demethylase 2A gene MP:0012744 increased neural crest cell apoptosis IAGP N RGD:5509061 20151217 MGI PMID:25463925 1616562 Lrfn4 leucine rich repeat and fibronectin type III domain containing 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20161027 MGI PMID:26321637 1616562 Lrfn4 leucine rich repeat and fibronectin type III domain containing 4 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20171116 MGI PMID:27480238 1616562 Lrfn4 leucine rich repeat and fibronectin type III domain containing 4 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20161027 MGI PMID:26321637 1616562 Lrfn4 leucine rich repeat and fibronectin type III domain containing 4 gene MP:0008035 behavioral arrest IAGP N RGD:5509061 20161027 MGI PMID:26321637 1616562 Lrfn4 leucine rich repeat and fibronectin type III domain containing 4 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20171116 MGI PMID:27480238 1616562 Lrfn4 leucine rich repeat and fibronectin type III domain containing 4 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20161027 MGI PMID:26321637 1616576 Trim58 tripartite motif-containing 58 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1616576 Trim58 tripartite motif-containing 58 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1616576 Trim58 tripartite motif-containing 58 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1616576 Trim58 tripartite motif-containing 58 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1616576 Trim58 tripartite motif-containing 58 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 1616576 Trim58 tripartite motif-containing 58 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1616576 Trim58 tripartite motif-containing 58 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20191024 MGI PMID:31383741 1616577 Clint1 clathrin interactor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1616578 A3galt2 alpha 1,3-galactosyltransferase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:17372206 1616585 Scgn secretagogin, EF-hand calcium binding protein gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20210603 MGI PMID:31663849 1616585 Scgn secretagogin, EF-hand calcium binding protein gene MP:0005381 digestive/alimentary phenotype IAGP N RGD:5509061 20210603 MGI PMID:31663849 1616585 Scgn secretagogin, EF-hand calcium binding protein gene MP:0010768 mortality/aging IAGP N RGD:5509061 20210603 MGI PMID:31663849 1616585 Scgn secretagogin, EF-hand calcium binding protein gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20210603 MGI PMID:31663849 1616586 Trim38 tripartite motif-containing 38 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20171109 MGI PMID:26392463 1616586 Trim38 tripartite motif-containing 38 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20171109 MGI PMID:26392463 1616586 Trim38 tripartite motif-containing 38 gene MP:0008573 increased circulating interferon-alpha level IAGP N RGD:5509061 20171109 MGI PMID:26392463 1616586 Trim38 tripartite motif-containing 38 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20171109 MGI PMID:26392463 1616586 Trim38 tripartite motif-containing 38 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20171109 MGI PMID:26392463 1616586 Trim38 tripartite motif-containing 38 gene MP:0009787 increased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20171109 MGI PMID:26392463 1616586 Trim38 tripartite motif-containing 38 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20171109 MGI PMID:26392463 1616587 Ago3 argonaute RISC catalytic subunit 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1616588 4933430I17Rik RIKEN cDNA 4933430I17 gene gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20160811 MGI 1616588 4933430I17Rik RIKEN cDNA 4933430I17 gene gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1616588 4933430I17Rik RIKEN cDNA 4933430I17 gene gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1616588 4933430I17Rik RIKEN cDNA 4933430I17 gene gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1616588 4933430I17Rik RIKEN cDNA 4933430I17 gene gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20211021 MGI 1616590 Ccdc62 coiled-coil domain containing 62 gene MP:0001925 male infertility IAGP N RGD:5509061 20180301 MGI PMID:28339613 1616590 Ccdc62 coiled-coil domain containing 62 gene MP:0001932 abnormal spermiogenesis IEA N RGD:5509061 20180301 MGI 1616590 Ccdc62 coiled-coil domain containing 62 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20180301 MGI PMID:28339613 1616590 Ccdc62 coiled-coil domain containing 62 gene MP:0002687 oligozoospermia IEA N RGD:5509061 20220714 MGI 1616590 Ccdc62 coiled-coil domain containing 62 gene MP:0004910 decreased seminal vesicle weight IEA N RGD:5509061 20180301 MGI 1616590 Ccdc62 coiled-coil domain containing 62 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20180301 MGI PMID:28339613 1616590 Ccdc62 coiled-coil domain containing 62 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20180405 MGI PMID:28339613 1616590 Ccdc62 coiled-coil domain containing 62 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20180301 MGI PMID:28339613 1616590 Ccdc62 coiled-coil domain containing 62 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20180301 MGI PMID:28339613 1616592 Klf11 Kruppel-like transcription factor 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15607700 1616592 Klf11 Kruppel-like transcription factor 11 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20190117 MGI PMID:23555910 1616592 Klf11 Kruppel-like transcription factor 11 gene MP:0009221 uterus adenomyosis IAGP N RGD:5509061 20190117 MGI PMID:23555910 1616634 Acot2 acyl-CoA thioesterase 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1616634 Acot2 acyl-CoA thioesterase 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200310 MGI 1616643 Zfta zinc finger translocation associated gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20220224 MGI PMID:35087169 1616644 Ankhd1 ankyrin repeat and KH domain containing 1 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1616644 Ankhd1 ankyrin repeat and KH domain containing 1 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20181227 MGI 1616647 Flacc1 flagellum associated containing coiled-coil domains 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20240523 MGI 1616647 Flacc1 flagellum associated containing coiled-coil domains 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20240523 MGI 1616647 Flacc1 flagellum associated containing coiled-coil domains 1 gene MP:0002989 small kidney IEA N RGD:5509061 20240523 MGI 1616648 Ccdc122 coiled-coil domain containing 122 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150430 MGI 1616648 Ccdc122 coiled-coil domain containing 122 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1616648 Ccdc122 coiled-coil domain containing 122 gene MP:0010052 increased grip strength IEA N RGD:5509061 20150430 MGI 1616648 Ccdc122 coiled-coil domain containing 122 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 1616648 Ccdc122 coiled-coil domain containing 122 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1616648 Ccdc122 coiled-coil domain containing 122 gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20210128 MGI 1616648 Ccdc122 coiled-coil domain containing 122 gene MP:0011939 increased food intake IEA N RGD:5509061 20210128 MGI 1616649 Spem2 SPEM family member 2 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0009839 multiflagellated sperm IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0014468 disorganized sperm mitochondrial sheath IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0031009 abnormal sperm-egg fusion IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0031372 abnormal sperm individualization IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616649 Spem2 SPEM family member 2 gene MP:0031408 multi-headed sperm IAGP N RGD:5509061 20241024 MGI PMID:38421455 1616651 Mylk myosin, light polypeptide kinase gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:24151072 1616651 Mylk myosin, light polypeptide kinase gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:24151072 1616651 Mylk myosin, light polypeptide kinase gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24151072 1616651 Mylk myosin, light polypeptide kinase gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0003622 ischuria IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0004036 abnormal muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:16461919 1616651 Mylk myosin, light polypeptide kinase gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:12730364 1616651 Mylk myosin, light polypeptide kinase gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16461919 1616651 Mylk myosin, light polypeptide kinase gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0008802 abnormal intestinal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0009485 distended ileum IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0011082 abnormal gastrointestinal motility IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24151072 1616651 Mylk myosin, light polypeptide kinase gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24151072 1616651 Mylk myosin, light polypeptide kinase gene MP:0011503 distended jejunum IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616651 Mylk myosin, light polypeptide kinase gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:18586037 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20240523 MGI 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20191128 MGI PMID:29718757 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0001925 male infertility IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0002766 situs inversus IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20191128 MGI PMID:29718757 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210128 MGI 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0004133 heterotaxia IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20220811 MGI 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20191128 MGI PMID:29718757 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20191128 MGI PMID:29718757 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20191128 MGI PMID:29718757 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20191128 MGI PMID:29718757 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20191128 MGI PMID:29718757 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20191128 MGI PMID:29718757 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0020869 immotile sperm IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616652 Arl2bp ADP-ribosylation factor-like 2 binding protein gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20191128 MGI PMID:31425546 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20200310 MGI PMID:24680895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20200310 MGI PMID:17079737 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001148 enlarged testis IAGP N RGD:5509061 20200310 MGI PMID:15192078 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20200310 MGI PMID:24680895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:15192078 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20200310 MGI PMID:17850793 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001304 cataract IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001306 small lens IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:16785743 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:17079737 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20200310 MGI PMID:17079737 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:17079737 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001924 infertility IAGP N RGD:5509061 20200310 MGI PMID:15192078 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:17079737 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:16785743 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21727895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:15192078 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:16785743 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20200310 MGI PMID:17079737 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0002546 mydriasis IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0002579 disorganized secondary lens fibers IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20200310 MGI PMID:17079737 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20200310 MGI PMID:17079737 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0002673 abnormal sperm number IAGP N RGD:5509061 20200310 MGI PMID:17079737 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:17079737 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20200310 MGI PMID:24680895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20200310 MGI PMID:15192078 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:16785743 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:21523854 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:17850793 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0003595 epididymal cyst IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:21523854 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:24680895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20200310 MGI PMID:24680895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20200310 MGI PMID:16785743 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20200310 MGI PMID:15192078 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20200310 MGI PMID:16785743 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20200310 MGI PMID:24680895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0004223 hypoplastic trabecular meshwork IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20200310 MGI PMID:16785743 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0004728 abnormal efferent ductules of testis morphology IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20200310 MGI PMID:17079737 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20200310 MGI PMID:15192078 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20200310 MGI PMID:17079737 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0004932 epididymis hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:21523854 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0005204 abnormal canal of Schlemm morphology IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0005544 cornea deposits IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20200310 MGI PMID:16785743 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0006230 iris stroma hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0006416 abnormal rete testis morphology IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0006417 rete testis obstruction IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0006423 dilated rete testis IAGP N RGD:5509061 20200310 MGI PMID:17079737 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20200310 MGI PMID:21727895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20200310 MGI PMID:16785743 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0009248 small caput epididymis IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20200310 MGI PMID:16785743 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20200310 MGI PMID:21727895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20200310 MGI PMID:24680895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:21727895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20200310 MGI PMID:24680895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20200310 MGI PMID:22738954 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011006 abnormal epidermal stem cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:24680895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17079737 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16785743 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21523854 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24680895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15192078 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16785743 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24680895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16785743 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21523854 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011365 small metanephros IAGP N RGD:5509061 20200310 MGI PMID:21523854 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20200310 MGI PMID:22738954 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:24680895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011457 abnormal metanephric ureteric bud development IAGP N RGD:5509061 20200310 MGI PMID:21523854 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011499 abnormal glomerular capsule space morphology IAGP N RGD:5509061 20200310 MGI PMID:24680895 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:17079737 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0013743 ciliary body hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0014193 decreased epididymal cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:16406039 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616653 Lgr4 leucine-rich repeat-containing G protein-coupled receptor 4 gene MP:0020858 cornea epithelium hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:18424556 1616657 Slc25a47 solute carrier family 25, member 47 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230601 MGI 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20160512 MGI PMID:25770585 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0001192 scaly skin IEA N RGD:5509061 20210520 MGI 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20201022 MGI 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160512 MGI PMID:25770585 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20160512 MGI PMID:25770585 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0008762 embryonic lethality IEA N RGD:5509061 20141003 MGI 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20160512 MGI PMID:25770585 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20160512 MGI PMID:25770585 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0011103 embryonic lethality at implantation, incomplete penetrance IAGP N RGD:5509061 20160512 MGI PMID:25770585 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20160512 MGI PMID:25770585 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20240118 MGI PMID:36638184 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20240118 MGI PMID:36638184 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20240118 MGI PMID:36638184 1616658 Smg6 SMG6 nonsense mediated mRNA decay factor gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20240118 MGI PMID:36638184 1616660 Myzap myocardial zonula adherens protein gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1616660 Myzap myocardial zonula adherens protein gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20180614 MGI PMID:26719331 1616660 Myzap myocardial zonula adherens protein gene MP:0002833 increased heart weight IAGP N RGD:5509061 20180614 MGI PMID:26719331 1616660 Myzap myocardial zonula adherens protein gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20180614 MGI PMID:26719331 1616660 Myzap myocardial zonula adherens protein gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20180614 MGI PMID:26719331 1616660 Myzap myocardial zonula adherens protein gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1616660 Myzap myocardial zonula adherens protein gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20180614 MGI PMID:26719331 1616660 Myzap myocardial zonula adherens protein gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1616660 Myzap myocardial zonula adherens protein gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1616660 Myzap myocardial zonula adherens protein gene MP:0005630 increased lung weight IAGP N RGD:5509061 20180614 MGI PMID:26719331 1616660 Myzap myocardial zonula adherens protein gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180614 MGI PMID:26719331 1616660 Myzap myocardial zonula adherens protein gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20180614 MGI PMID:26719331 1616660 Myzap myocardial zonula adherens protein gene MP:0030610 absent teeth IEA N RGD:5509061 20240523 MGI 1616663 Clca4b chloride channel accessory 4B gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170323 MGI 1616666 Celrr cerebellum expressed regulatory RNA gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:24381249 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20200310 MGI 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20240523 MGI 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20240523 MGI 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:24931609 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:24931609 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:24931609 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200310 MGI 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200310 MGI PMID:24931609 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0004002 abnormal jejunum morphology IEA N RGD:5509061 20240523 MGI 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20200310 MGI PMID:24931609 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:24931609 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200310 MGI PMID:24931609 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:24931609 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20200310 MGI PMID:24931609 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:24931609 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:24931609 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:24931609 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20200310 MGI PMID:24931609 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20200310 MGI PMID:24931609 1616667 Nucks1 nuclear casein kinase and cyclin-dependent kinase substrate 1 gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20200310 MGI PMID:24931609 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0000601 small liver IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20210826 MGI 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0001577 anemia IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0002083 premature death IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20181227 MGI 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20181227 MGI 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0011952 decreased cardiac stroke volume IEA N RGD:5509061 20210520 MGI 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0012236 abnormal cholangiocyte morphology IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0012242 abnormal hepatoblast differentiation IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0012246 abnormal hepatic cord morphology IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1616671 Cdk5rap3 CDK5 regulatory subunit associated protein 3 gene MP:0013693 abnormal hemopoiesis IAGP N RGD:5509061 20190516 MGI PMID:30635284 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20201022 MGI 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20170608 MGI PMID:25332286 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20170608 MGI PMID:25332286 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20170608 MGI PMID:25332286 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0003405 abnormal platelet shape IAGP N RGD:5509061 20170608 MGI PMID:25332286 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20170608 MGI PMID:25332286 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20170608 MGI PMID:25332286 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20170608 MGI PMID:25332286 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20170608 MGI PMID:25332286 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20170608 MGI PMID:25332286 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20170608 MGI PMID:25332286 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20170608 MGI PMID:25332286 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0009676 abnormal hemostasis IAGP N RGD:5509061 20170608 MGI PMID:25332286 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0014060 abnormal platelet alpha-granule morphology IAGP N RGD:5509061 20170608 MGI PMID:25332286 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0020431 decreased platelet alpha-granule number IAGP N RGD:5509061 20170720 MGI PMID:25332286 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:26829768 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0020928 increased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:26829768 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:26829768 1616676 Agbl4 ATP/GTP binding protein-like 4 gene MP:0031034 increased susceptibility to Poxviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:26829768 1616678 Gas2l1 growth arrest-specific 2 like 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1616678 Gas2l1 growth arrest-specific 2 like 1 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1616678 Gas2l1 growth arrest-specific 2 like 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1616678 Gas2l1 growth arrest-specific 2 like 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1616678 Gas2l1 growth arrest-specific 2 like 1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20181227 MGI 1616678 Gas2l1 growth arrest-specific 2 like 1 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20181227 MGI 1616679 Chsy3 chondroitin sulfate synthase 3 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20201022 MGI 1616679 Chsy3 chondroitin sulfate synthase 3 gene MP:0001200 thick skin IEA N RGD:5509061 20181227 MGI 1616679 Chsy3 chondroitin sulfate synthase 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20181227 MGI 1616679 Chsy3 chondroitin sulfate synthase 3 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1616679 Chsy3 chondroitin sulfate synthase 3 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1616679 Chsy3 chondroitin sulfate synthase 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1616679 Chsy3 chondroitin sulfate synthase 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1616679 Chsy3 chondroitin sulfate synthase 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1616679 Chsy3 chondroitin sulfate synthase 3 gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 1616679 Chsy3 chondroitin sulfate synthase 3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20181227 MGI 1616679 Chsy3 chondroitin sulfate synthase 3 gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 1616679 Chsy3 chondroitin sulfate synthase 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1616679 Chsy3 chondroitin sulfate synthase 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1616679 Chsy3 chondroitin sulfate synthase 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1616682 Mmab methylmalonic aciduria (cobalamin deficiency) cblB type homolog (human) gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1616682 Mmab methylmalonic aciduria (cobalamin deficiency) cblB type homolog (human) gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20230119 MGI 1616682 Mmab methylmalonic aciduria (cobalamin deficiency) cblB type homolog (human) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1616685 Defb41 defensin beta 41 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22701646 1616685 Defb41 defensin beta 41 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22701646 1616685 Defb41 defensin beta 41 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:22701646 1616685 Defb41 defensin beta 41 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22701646 1616685 Defb41 defensin beta 41 gene MP:0004728 abnormal efferent ductules of testis morphology IAGP N RGD:5509061 20141003 MGI PMID:22701646 1616685 Defb41 defensin beta 41 gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:22701646 1616685 Defb41 defensin beta 41 gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22701646 1616685 Defb41 defensin beta 41 gene MP:0009140 dilated efferent ductule of testis IAGP N RGD:5509061 20141003 MGI PMID:22701646 1616685 Defb41 defensin beta 41 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22701646 1616685 Defb41 defensin beta 41 gene MP:0014194 increased epididymal epithelium cell proliferation IAGP N RGD:5509061 20160526 MGI PMID:22701646 1616691 Trat1 T cell receptor associated transmembrane adaptor 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16612002 1616691 Trat1 T cell receptor associated transmembrane adaptor 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16612002 1616691 Trat1 T cell receptor associated transmembrane adaptor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16612002 1616691 Trat1 T cell receptor associated transmembrane adaptor 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16612002 1616691 Trat1 T cell receptor associated transmembrane adaptor 1 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16612002 1616692 Steep1 STING1 ER exit protein 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20111116 MGI 1616692 Steep1 STING1 ER exit protein 1 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IEA N RGD:5509061 20141003 MGI 1616692 Steep1 STING1 ER exit protein 1 gene MP:0012138 decreased forebrain size IEA N RGD:5509061 20141003 MGI 1616693 Prelid2 PRELI domain containing 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20160811 MGI 1616693 Prelid2 PRELI domain containing 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1616695 Il31 interleukin 31 gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 1616695 Il31 interleukin 31 gene MP:0010073 decreased pruritus IAGP N RGD:5509061 20240704 MGI PMID:29703903 1616704 Mtif3 mitochondrial translational initiation factor 3 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1616704 Mtif3 mitochondrial translational initiation factor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240222 MGI PMID:31903419 1616704 Mtif3 mitochondrial translational initiation factor 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1616704 Mtif3 mitochondrial translational initiation factor 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20240222 MGI PMID:31903419 1616704 Mtif3 mitochondrial translational initiation factor 3 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20210128 MGI 1616704 Mtif3 mitochondrial translational initiation factor 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20240222 MGI PMID:31903419 1616704 Mtif3 mitochondrial translational initiation factor 3 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20240222 MGI PMID:31903419 1616704 Mtif3 mitochondrial translational initiation factor 3 gene MP:0006206 embryonic lethality between somite formation and embryo turning IAGP N RGD:5509061 20240222 MGI PMID:31903419 1616704 Mtif3 mitochondrial translational initiation factor 3 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20240222 MGI PMID:31903419 1616704 Mtif3 mitochondrial translational initiation factor 3 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20240222 MGI PMID:31903419 1616704 Mtif3 mitochondrial translational initiation factor 3 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20240222 MGI PMID:31903419 1616704 Mtif3 mitochondrial translational initiation factor 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616704 Mtif3 mitochondrial translational initiation factor 3 gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20240222 MGI PMID:31903419 1616705 Trmt5 TRM5 tRNA methyltransferase 5 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1616705 Trmt5 TRM5 tRNA methyltransferase 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20221215 MGI 1616706 Slc18b1 solute carrier family 18, subfamily B, member 1 gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20200123 MGI PMID:31800589 1616706 Slc18b1 solute carrier family 18, subfamily B, member 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20200123 MGI PMID:31800589 1616706 Slc18b1 solute carrier family 18, subfamily B, member 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20200123 MGI PMID:31800589 1616706 Slc18b1 solute carrier family 18, subfamily B, member 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20200123 MGI PMID:31800589 1616706 Slc18b1 solute carrier family 18, subfamily B, member 1 gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20200123 MGI PMID:31800589 1616706 Slc18b1 solute carrier family 18, subfamily B, member 1 gene MP:0012315 impaired learning IAGP N RGD:5509061 20200123 MGI PMID:31800589 1616706 Slc18b1 solute carrier family 18, subfamily B, member 1 gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:31800589 1616706 Slc18b1 solute carrier family 18, subfamily B, member 1 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:31800589 1616706 Slc18b1 solute carrier family 18, subfamily B, member 1 gene MP:0030585 enhanced behavioral response to amphetamine IAGP N RGD:5509061 20200123 MGI PMID:31800589 1616707 Pcnp PEST proteolytic signal containing nuclear protein gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1616707 Pcnp PEST proteolytic signal containing nuclear protein gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20201022 MGI 1616707 Pcnp PEST proteolytic signal containing nuclear protein gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1616707 Pcnp PEST proteolytic signal containing nuclear protein gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20201022 MGI 1616707 Pcnp PEST proteolytic signal containing nuclear protein gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1616707 Pcnp PEST proteolytic signal containing nuclear protein gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20201022 MGI 1616707 Pcnp PEST proteolytic signal containing nuclear protein gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20201022 MGI 1616707 Pcnp PEST proteolytic signal containing nuclear protein gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20201022 MGI 1616707 Pcnp PEST proteolytic signal containing nuclear protein gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20201022 MGI 1616707 Pcnp PEST proteolytic signal containing nuclear protein gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20201022 MGI 1616707 Pcnp PEST proteolytic signal containing nuclear protein gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1616707 Pcnp PEST proteolytic signal containing nuclear protein gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 1616707 Pcnp PEST proteolytic signal containing nuclear protein gene MP:0009806 abnormal otic vesicle morphology IEA N RGD:5509061 20230601 MGI 1616707 Pcnp PEST proteolytic signal containing nuclear protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616707 Pcnp PEST proteolytic signal containing nuclear protein gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1616711 Bltp3b bridge-like lipid transfer protein family member 3B gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:20551173 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0001147 small testis IEA N RGD:5509061 20230119 MGI 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:20551173 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:20551173 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:20551173 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:20551173 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:20551173 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:20551173 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:20551173 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20230420 MGI PMID:31000436 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:20551173 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20551173 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0009205 abnormal internal male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:20551173 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20141003 MGI PMID:20551173 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:20551173 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20551173 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20551173 1616719 Mei4 meiotic double-stranded break formation protein 4 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20150312 MGI PMID:20551173 1616720 Ct55 cancer/testis antigen 55 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0001925 male infertility IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20191128 MGI PMID:30944312 1616720 Ct55 cancer/testis antigen 55 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20191128 MGI PMID:30944312 1616720 Ct55 cancer/testis antigen 55 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20191128 MGI PMID:30944312 1616720 Ct55 cancer/testis antigen 55 gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616720 Ct55 cancer/testis antigen 55 gene MP:0031372 abnormal sperm individualization IAGP N RGD:5509061 20230727 MGI PMID:36481789 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20200924 MGI PMID:32529245 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0001925 male infertility IAGP N RGD:5509061 20200924 MGI PMID:32529245 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0001925 male infertility IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200924 MGI PMID:32529245 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220915 MGI PMID:35547804 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20200924 MGI PMID:32529245 1616722 Tmprss12 transmembrane (C-terminal) protease, serine 12 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20200924 MGI PMID:32529245 1616725 Shld1 shieldin complex subunit 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1616725 Shld1 shieldin complex subunit 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1616725 Shld1 shieldin complex subunit 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1616725 Shld1 shieldin complex subunit 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1616725 Shld1 shieldin complex subunit 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1616725 Shld1 shieldin complex subunit 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1616725 Shld1 shieldin complex subunit 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1616725 Shld1 shieldin complex subunit 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1616725 Shld1 shieldin complex subunit 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1616725 Shld1 shieldin complex subunit 1 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 1616725 Shld1 shieldin complex subunit 1 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 1616725 Shld1 shieldin complex subunit 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20210826 MGI PMID:33857404 1616725 Shld1 shieldin complex subunit 1 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210826 MGI 1616725 Shld1 shieldin complex subunit 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1616725 Shld1 shieldin complex subunit 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1616725 Shld1 shieldin complex subunit 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20210826 MGI PMID:33857404 1616725 Shld1 shieldin complex subunit 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19364920 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19364920 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19364920 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:19364920 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0001872 sinus inflammation IAGP N RGD:5509061 20141003 MGI PMID:19364920 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19364920 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0002274 abnormal type I pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:19364920 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0004391 abnormal respiratory conducting tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19364920 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19364920 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20141003 MGI PMID:19364920 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0010809 abnormal club cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0010891 increased alveolar lamellar body number IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0010896 decreased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0010901 abnormal pulmonary alveolar parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0010936 decreased airway resistance IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0010942 abnormal respiratory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19364920 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0010942 abnormal respiratory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0010950 abnormal lung hysteresivity IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0011044 increased lung elastance IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0011047 increased lung tissue damping IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0011053 decreased respiratory motile cilia number IAGP N RGD:5509061 20141003 MGI PMID:19364920 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0011053 decreased respiratory motile cilia number IAGP N RGD:5509061 20141003 MGI PMID:21049041 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19364920 1616726 Cby1 chibby family member 1, beta catenin antagonist gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20200206 MGI PMID:17403895 1616729 Zfp383 zinc finger protein 383 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1616729 Zfp383 zinc finger protein 383 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1616733 Rbm20 RNA binding motif protein 20 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20220519 MGI PMID:35394688 1616733 Rbm20 RNA binding motif protein 20 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20201217 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0000277 abnormal heart shape IEA N RGD:5509061 20221215 MGI 1616733 Rbm20 RNA binding motif protein 20 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:24599837 1616733 Rbm20 RNA binding motif protein 20 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20201217 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0000692 small spleen IEA N RGD:5509061 20221215 MGI 1616733 Rbm20 RNA binding motif protein 20 gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1616733 Rbm20 RNA binding motif protein 20 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1616733 Rbm20 RNA binding motif protein 20 gene MP:0001333 absent optic nerve IEA N RGD:5509061 20221215 MGI 1616733 Rbm20 RNA binding motif protein 20 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210520 MGI 1616733 Rbm20 RNA binding motif protein 20 gene MP:0002083 premature death IAGP N RGD:5509061 20201217 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0002083 premature death IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0002083 premature death IAGP N RGD:5509061 20220519 MGI PMID:35394688 1616733 Rbm20 RNA binding motif protein 20 gene MP:0002332 abnormal exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:24599837 1616733 Rbm20 RNA binding motif protein 20 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1616733 Rbm20 RNA binding motif protein 20 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20220519 MGI PMID:35394688 1616733 Rbm20 RNA binding motif protein 20 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20201217 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20220519 MGI PMID:35394688 1616733 Rbm20 RNA binding motif protein 20 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:24599837 1616733 Rbm20 RNA binding motif protein 20 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20201217 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20201217 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20201217 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0003901 abnormal PR interval IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:24599837 1616733 Rbm20 RNA binding motif protein 20 gene MP:0004009 abnormal diastolic filling velocity IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0004070 abnormal P wave IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20201217 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0004085 abnormal heartbeat IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:24599837 1616733 Rbm20 RNA binding motif protein 20 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:24599837 1616733 Rbm20 RNA binding motif protein 20 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20201217 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0006110 ventricular fibrillation IAGP N RGD:5509061 20201217 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0008543 atrial fibrillation IAGP N RGD:5509061 20201217 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20220519 MGI PMID:35394688 1616733 Rbm20 RNA binding motif protein 20 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20201217 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0009084 blind uterus IEA N RGD:5509061 20210520 MGI 1616733 Rbm20 RNA binding motif protein 20 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20201217 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0010504 abnormal RR interval IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20220519 MGI PMID:35041844 1616733 Rbm20 RNA binding motif protein 20 gene MP:0011919 abnormal R wave IAGP N RGD:5509061 20201217 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20201217 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20220519 MGI PMID:35394688 1616733 Rbm20 RNA binding motif protein 20 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:24599837 1616733 Rbm20 RNA binding motif protein 20 gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231221 MGI PMID:35394688 1616733 Rbm20 RNA binding motif protein 20 gene MP:0031302 syncope IAGP N RGD:5509061 20211028 MGI PMID:33110103 1616733 Rbm20 RNA binding motif protein 20 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:35041844 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21896782 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:21896782 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:21896782 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:21896782 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21896782 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:21896782 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0003718 maternal effect IAGP N RGD:5509061 20220120 MGI PMID:34931676 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21896782 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21896782 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:21896782 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21896782 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21896782 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21896782 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20220120 MGI PMID:34931676 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21896782 1616734 Dppa2 developmental pluripotency associated 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21896782 1616739 Lypd3 Ly6/Plaur domain containing 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:27169360 1616739 Lypd3 Ly6/Plaur domain containing 3 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20200310 MGI 1616739 Lypd3 Ly6/Plaur domain containing 3 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20200310 MGI PMID:27169360 1616739 Lypd3 Ly6/Plaur domain containing 3 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20200310 MGI PMID:27169360 1616739 Lypd3 Ly6/Plaur domain containing 3 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20200310 MGI PMID:27169360 1616739 Lypd3 Ly6/Plaur domain containing 3 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20200310 MGI 1616739 Lypd3 Ly6/Plaur domain containing 3 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:27169360 1616739 Lypd3 Ly6/Plaur domain containing 3 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20200310 MGI PMID:27169360 1616739 Lypd3 Ly6/Plaur domain containing 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20200310 MGI 1616739 Lypd3 Ly6/Plaur domain containing 3 gene MP:0011939 increased food intake IEA N RGD:5509061 20210128 MGI 1616739 Lypd3 Ly6/Plaur domain containing 3 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20200310 MGI PMID:27169360 1616739 Lypd3 Ly6/Plaur domain containing 3 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20200310 MGI PMID:27169360 1616741 Ift70b intraflagellar transport 70B gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1616743 Zdhhc11 zinc finger, DHHC domain containing 11 gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20211021 MGI PMID:34490261 1616743 Zdhhc11 zinc finger, DHHC domain containing 11 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1616743 Zdhhc11 zinc finger, DHHC domain containing 11 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20211021 MGI PMID:34490261 1616743 Zdhhc11 zinc finger, DHHC domain containing 11 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20211021 MGI PMID:34490261 1616750 Cabyr calcium binding tyrosine phosphorylation regulated gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20180503 MGI PMID:27802166 1616750 Cabyr calcium binding tyrosine phosphorylation regulated gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20180503 MGI PMID:27802166 1616750 Cabyr calcium binding tyrosine phosphorylation regulated gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20180503 MGI PMID:27802166 1616750 Cabyr calcium binding tyrosine phosphorylation regulated gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20180503 MGI PMID:27802166 1616750 Cabyr calcium binding tyrosine phosphorylation regulated gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20180503 MGI PMID:27802166 1616750 Cabyr calcium binding tyrosine phosphorylation regulated gene MP:0009280 decreased activated sperm motility IAGP N RGD:5509061 20180503 MGI PMID:27802166 1616750 Cabyr calcium binding tyrosine phosphorylation regulated gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20180503 MGI PMID:27802166 1616750 Cabyr calcium binding tyrosine phosphorylation regulated gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20180503 MGI PMID:27802166 1616750 Cabyr calcium binding tyrosine phosphorylation regulated gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20180503 MGI PMID:27802166 1616750 Cabyr calcium binding tyrosine phosphorylation regulated gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20180621 MGI PMID:27802166 1616753 Glt6d1 glycosyltransferase 6 domain containing 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210708 MGI PMID:32561905 1616757 Polr3gl polymerase (RNA) III (DNA directed) polypeptide G like gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20201001 MGI PMID:32576691 1616757 Polr3gl polymerase (RNA) III (DNA directed) polypeptide G like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201001 MGI PMID:32576691 1616757 Polr3gl polymerase (RNA) III (DNA directed) polypeptide G like gene MP:0001393 ataxia IAGP N RGD:5509061 20201001 MGI PMID:32576691 1616757 Polr3gl polymerase (RNA) III (DNA directed) polypeptide G like gene MP:0001525 impaired balance IAGP N RGD:5509061 20201001 MGI PMID:32576691 1616757 Polr3gl polymerase (RNA) III (DNA directed) polypeptide G like gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1616757 Polr3gl polymerase (RNA) III (DNA directed) polypeptide G like gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20201002 MGI PMID:32576691 1616757 Polr3gl polymerase (RNA) III (DNA directed) polypeptide G like gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20201001 MGI PMID:32576691 1616757 Polr3gl polymerase (RNA) III (DNA directed) polypeptide G like gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20201001 MGI PMID:32576691 1616757 Polr3gl polymerase (RNA) III (DNA directed) polypeptide G like gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20201002 MGI PMID:32576691 1616757 Polr3gl polymerase (RNA) III (DNA directed) polypeptide G like gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1616760 2010003K11Rik RIKEN cDNA 2010003K11 gene gene MP:0001260 increased body weight IAGP N RGD:5509061 20221222 MGI PMID:35093589 1616760 2010003K11Rik RIKEN cDNA 2010003K11 gene gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20221222 MGI PMID:35093589 1616760 2010003K11Rik RIKEN cDNA 2010003K11 gene gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20221222 MGI PMID:35093589 1616760 2010003K11Rik RIKEN cDNA 2010003K11 gene gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20221222 MGI PMID:35093589 1616760 2010003K11Rik RIKEN cDNA 2010003K11 gene gene MP:0002981 increased liver weight IAGP N RGD:5509061 20221222 MGI PMID:35093589 1616760 2010003K11Rik RIKEN cDNA 2010003K11 gene gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20221222 MGI PMID:35093589 1616760 2010003K11Rik RIKEN cDNA 2010003K11 gene gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20221222 MGI PMID:35093589 1616760 2010003K11Rik RIKEN cDNA 2010003K11 gene gene MP:0005331 insulin resistance IAGP N RGD:5509061 20221222 MGI PMID:35093589 1616760 2010003K11Rik RIKEN cDNA 2010003K11 gene gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20221222 MGI PMID:35093589 1616760 2010003K11Rik RIKEN cDNA 2010003K11 gene gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20221222 MGI PMID:35093589 1616760 2010003K11Rik RIKEN cDNA 2010003K11 gene gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20221222 MGI PMID:35093589 1616760 2010003K11Rik RIKEN cDNA 2010003K11 gene gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20221222 MGI PMID:35093589 1616760 2010003K11Rik RIKEN cDNA 2010003K11 gene gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20221222 MGI PMID:35093589 1616760 2010003K11Rik RIKEN cDNA 2010003K11 gene gene MP:0031269 increased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20221222 MGI PMID:35093589 1616761 Rab43 RAB43, member RAS oncogene family gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1616761 Rab43 RAB43, member RAS oncogene family gene MP:0002455 abnormal dendritic cell antigen presentation IEA N RGD:5509061 20161201 MGI 1616761 Rab43 RAB43, member RAS oncogene family gene MP:0002833 increased heart weight IEA N RGD:5509061 20231207 MGI 1616761 Rab43 RAB43, member RAS oncogene family gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1616761 Rab43 RAB43, member RAS oncogene family gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1616761 Rab43 RAB43, member RAS oncogene family gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20221215 MGI 1616764 Clec4b1 C-type lectin domain family 4, member b1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20191128 MGI PMID:27887882 1616764 Clec4b1 C-type lectin domain family 4, member b1 gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20191128 MGI PMID:27887882 1616764 Clec4b1 C-type lectin domain family 4, member b1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20191128 MGI PMID:27887882 1616764 Clec4b1 C-type lectin domain family 4, member b1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20191128 MGI PMID:27887882 1616764 Clec4b1 C-type lectin domain family 4, member b1 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20191128 MGI PMID:27887882 1616764 Clec4b1 C-type lectin domain family 4, member b1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20191128 MGI PMID:27887882 1616765 Pou2af2 POU domain, class 2, associating factor 2 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20230720 MGI PMID:35576971 1616765 Pou2af2 POU domain, class 2, associating factor 2 gene MP:0000537 abnormal urethra morphology IAGP N RGD:5509061 20230720 MGI PMID:35576971 1616765 Pou2af2 POU domain, class 2, associating factor 2 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20230720 MGI PMID:35576971 1616765 Pou2af2 POU domain, class 2, associating factor 2 gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20230720 MGI PMID:35576971 1616765 Pou2af2 POU domain, class 2, associating factor 2 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20230720 MGI PMID:35576971 1616765 Pou2af2 POU domain, class 2, associating factor 2 gene MP:0009492 abnormal gallbladder epithelium morphology IAGP N RGD:5509061 20230720 MGI PMID:35576971 1616765 Pou2af2 POU domain, class 2, associating factor 2 gene MP:0010942 abnormal respiratory epithelium morphology IAGP N RGD:5509061 20230720 MGI PMID:35576971 1616765 Pou2af2 POU domain, class 2, associating factor 2 gene MP:0014353 abnormal gastrointestinal brush cell morphology IAGP N RGD:5509061 20240104 MGI PMID:35576971 1616765 Pou2af2 POU domain, class 2, associating factor 2 gene MP:0014354 abnormal respiratory tract brush cell morphology IAGP N RGD:5509061 20240104 MGI PMID:35576971 1616766 Syf2 SYF2 homolog, RNA splicing factor (S. cerevisiae) gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20200310 MGI PMID:22448250 1616766 Syf2 SYF2 homolog, RNA splicing factor (S. cerevisiae) gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20200310 MGI PMID:22448250 1616766 Syf2 SYF2 homolog, RNA splicing factor (S. cerevisiae) gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20200310 MGI PMID:22448250 1616766 Syf2 SYF2 homolog, RNA splicing factor (S. cerevisiae) gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20200310 MGI PMID:22448250 1616766 Syf2 SYF2 homolog, RNA splicing factor (S. cerevisiae) gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22448250 1616767 Mocos molybdenum cofactor sulfurase gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0001265 decreased body size IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1616767 Mocos molybdenum cofactor sulfurase gene MP:0001577 anemia IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0002083 premature death IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0002176 increased brain weight IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0002708 nephrolithiasis IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0002989 small kidney IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0003587 ureter obstruction IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0003606 kidney failure IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0004969 pale kidney IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1616767 Mocos molybdenum cofactor sulfurase gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0008822 decreased blood uric acid level IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1616767 Mocos molybdenum cofactor sulfurase gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0011335 abnormal kidney pelvis smooth muscle morphology IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0011336 abnormal kidney pelvis urothelium morphology IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0011402 renal cast IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0011413 colorless urine IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20230720 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20230727 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0031479 increased urine xanthine level IAGP N RGD:5509061 20230810 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0031484 increased urine hypoxanthine level IAGP N RGD:5509061 20230810 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0031487 increased circulating hypoxanthine level IAGP N RGD:5509061 20230810 MGI PMID:35372998 1616767 Mocos molybdenum cofactor sulfurase gene MP:0031490 increased circulating xanthine level IAGP N RGD:5509061 20230810 MGI PMID:35372998 1616768 Tmed10 transmembrane p24 trafficking protein 10 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200310 MGI 1616768 Tmed10 transmembrane p24 trafficking protein 10 gene MP:0001147 small testis IEA N RGD:5509061 20200310 MGI 1616768 Tmed10 transmembrane p24 trafficking protein 10 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20200310 MGI 1616768 Tmed10 transmembrane p24 trafficking protein 10 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200310 MGI 1616768 Tmed10 transmembrane p24 trafficking protein 10 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10660306 1616768 Tmed10 transmembrane p24 trafficking protein 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616768 Tmed10 transmembrane p24 trafficking protein 10 gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20230824 MGI PMID:10660306 1616769 Nufip2 nuclear FMR1 interacting protein 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1616769 Nufip2 nuclear FMR1 interacting protein 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210826 MGI 1616769 Nufip2 nuclear FMR1 interacting protein 2 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20210520 MGI 1616769 Nufip2 nuclear FMR1 interacting protein 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 1616769 Nufip2 nuclear FMR1 interacting protein 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1616769 Nufip2 nuclear FMR1 interacting protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1616770 Dpm3 dolichyl-phosphate mannosyltransferase polypeptide 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1616770 Dpm3 dolichyl-phosphate mannosyltransferase polypeptide 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616770 Dpm3 dolichyl-phosphate mannosyltransferase polypeptide 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1616770 Dpm3 dolichyl-phosphate mannosyltransferase polypeptide 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220519 MGI 1616772 Uckl1 uridine-cytidine kinase 1-like 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1616772 Uckl1 uridine-cytidine kinase 1-like 1 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1616772 Uckl1 uridine-cytidine kinase 1-like 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0000706 small thymus IEA N RGD:5509061 20210128 MGI 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20210128 MGI 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20181227 MGI 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170119 MGI PMID:26692198 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20170119 MGI PMID:26692198 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21593423 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210520 MGI 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20170119 MGI PMID:26692198 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:21593423 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0003711 pathological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:21593423 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210520 MGI 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20170119 MGI PMID:26692198 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20170119 MGI PMID:26692198 1616775 Ecscr endothelial cell surface expressed chemotaxis and apoptosis regulator gene MP:0020322 decreased vascular endothelial cell apoptosis IAGP N RGD:5509061 20160616 MGI PMID:21593423 1616777 Tmem109 transmembrane protein 109 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20060811 1616779 Tomm5 translocase of outer mitochondrial membrane 5 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22688586 1616779 Tomm5 translocase of outer mitochondrial membrane 5 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:22688586 1616779 Tomm5 translocase of outer mitochondrial membrane 5 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:22688586 1616779 Tomm5 translocase of outer mitochondrial membrane 5 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22688586 1616779 Tomm5 translocase of outer mitochondrial membrane 5 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22688586 1616779 Tomm5 translocase of outer mitochondrial membrane 5 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22688586 1616779 Tomm5 translocase of outer mitochondrial membrane 5 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:22688586 1616779 Tomm5 translocase of outer mitochondrial membrane 5 gene MP:0010904 abnormal alveolar pore morphology IAGP N RGD:5509061 20141003 MGI PMID:22688586 1616779 Tomm5 translocase of outer mitochondrial membrane 5 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22688586 1616780 Dcdc2c doublecortin domain containing 2C gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20210128 MGI 1616780 Dcdc2c doublecortin domain containing 2C gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1616781 Vps51 VPS51 GARP complex subunit gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1616781 Vps51 VPS51 GARP complex subunit gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1616781 Vps51 VPS51 GARP complex subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616782 Ccdc137 coiled-coil domain containing 137 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616783 Washc3 WASH complex subunit 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1616783 Washc3 WASH complex subunit 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616783 Washc3 WASH complex subunit 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1616783 Washc3 WASH complex subunit 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1616785 Cmtm5 CKLF-like MARVEL transmembrane domain containing 5 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20220908 MGI PMID:35274615 1616785 Cmtm5 CKLF-like MARVEL transmembrane domain containing 5 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20220908 MGI PMID:35274615 1616785 Cmtm5 CKLF-like MARVEL transmembrane domain containing 5 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20220908 MGI PMID:35274615 1616785 Cmtm5 CKLF-like MARVEL transmembrane domain containing 5 gene MP:0008918 microgliosis IAGP N RGD:5509061 20220908 MGI PMID:35274615 1616785 Cmtm5 CKLF-like MARVEL transmembrane domain containing 5 gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20220908 MGI PMID:35274615 1616788 Cinp cyclin dependent kinase 2 interacting protein gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1616788 Cinp cyclin dependent kinase 2 interacting protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616788 Cinp cyclin dependent kinase 2 interacting protein gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 1616788 Cinp cyclin dependent kinase 2 interacting protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1616788 Cinp cyclin dependent kinase 2 interacting protein gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0000469 abnormal esophageal squamous epithelium morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0000649 sebaceous gland atrophy IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0001221 epidermal atrophy IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0001505 hunched posture IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0001577 anemia IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0003278 esophageal inflammation IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0013139 moribund IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0013585 thymus cortex atrophy IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0013586 thymus medulla atrophy IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616789 Rnpc3 RNA-binding region (RNP1, RRM) containing 3 gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20190221 MGI PMID:30254136 1616791 Srfbp1 serum response factor binding protein 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241017 MGI 1616791 Srfbp1 serum response factor binding protein 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241017 MGI 1616791 Srfbp1 serum response factor binding protein 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241017 MGI 1616791 Srfbp1 serum response factor binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1616791 Srfbp1 serum response factor binding protein 1 gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20241017 MGI 1616792 Med18 mediator complex subunit 18 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20160804 MGI 1616792 Med18 mediator complex subunit 18 gene MP:0003062 abnormal coping response IEA N RGD:5509061 20160804 MGI 1616795 Lima1 LIM domain and actin binding 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20180830 MGI PMID:29880681 1616795 Lima1 LIM domain and actin binding 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20180830 MGI PMID:29880681 1616795 Lima1 LIM domain and actin binding 1 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20180830 MGI PMID:29880681 1616795 Lima1 LIM domain and actin binding 1 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20180830 MGI PMID:29880681 1616795 Lima1 LIM domain and actin binding 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180830 MGI PMID:29880681 1616795 Lima1 LIM domain and actin binding 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20180830 MGI PMID:29880681 1616795 Lima1 LIM domain and actin binding 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1616795 Lima1 LIM domain and actin binding 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1616796 Map3k20 mitogen-activated protein kinase kinase kinase 20 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20170713 MGI PMID:26755636 1616796 Map3k20 mitogen-activated protein kinase kinase kinase 20 gene MP:0000562 polydactyly IAGP N RGD:5509061 20170713 MGI PMID:26755636 1616796 Map3k20 mitogen-activated protein kinase kinase kinase 20 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20170713 MGI PMID:26755636 1616796 Map3k20 mitogen-activated protein kinase kinase kinase 20 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20170713 MGI PMID:26755636 1616796 Map3k20 mitogen-activated protein kinase kinase kinase 20 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170713 MGI PMID:26755636 1616796 Map3k20 mitogen-activated protein kinase kinase kinase 20 gene MP:0012270 cardiac edema IAGP N RGD:5509061 20170713 MGI PMID:26755636 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0003087 absent allantois IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20181227 MGI 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20180628 MGI PMID:29566152 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0012724 absent head fold IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20181227 MGI 1616801 Mrps22 mitochondrial ribosomal protein S22 gene MP:0014246 decreased cellular ATP level IAGP N RGD:5509061 20241024 MGI PMID:32376682 1616802 Nisch nischarin gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20170105 MGI 1616802 Nisch nischarin gene MP:0000445 short snout IAGP N RGD:5509061 20171228 MGI PMID:28806779 1616802 Nisch nischarin gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20170105 MGI 1616802 Nisch nischarin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20171228 MGI PMID:28806779 1616802 Nisch nischarin gene MP:0001265 decreased body size IAGP N RGD:5509061 20171228 MGI PMID:28806779 1616802 Nisch nischarin gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1616802 Nisch nischarin gene MP:0001410 head bobbing IEA N RGD:5509061 20181227 MGI 1616802 Nisch nischarin gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210128 MGI 1616802 Nisch nischarin gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1616802 Nisch nischarin gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1616802 Nisch nischarin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20171228 MGI PMID:28806779 1616802 Nisch nischarin gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20171228 MGI PMID:28806779 1616802 Nisch nischarin gene MP:0001958 emphysema IAGP N RGD:5509061 20171228 MGI PMID:28806779 1616802 Nisch nischarin gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20190502 MGI 1616802 Nisch nischarin gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20201022 MGI 1616802 Nisch nischarin gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1616802 Nisch nischarin gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20171228 MGI PMID:28806779 1616802 Nisch nischarin gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1616802 Nisch nischarin gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1616802 Nisch nischarin gene MP:0006018 abnormal tympanic membrane morphology IAGP N RGD:5509061 20171228 MGI PMID:28806779 1616802 Nisch nischarin gene MP:0006325 impaired hearing IAGP N RGD:5509061 20171228 MGI PMID:28806779 1616802 Nisch nischarin gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1616802 Nisch nischarin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20171228 MGI PMID:28806779 1616802 Nisch nischarin gene MP:0011142 abnormal lung-associated mesenchyme development IAGP N RGD:5509061 20171228 MGI PMID:28806779 1616802 Nisch nischarin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20171228 MGI PMID:28806779 1616802 Nisch nischarin gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20221215 MGI 1616803 Il20 interleukin 20 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230601 MGI 1616803 Il20 interleukin 20 gene MP:0002534 abnormal type IV hypersensitivity reaction IEA N RGD:5509061 20170323 MGI 1616803 Il20 interleukin 20 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1616804 Klrc3 killer cell lectin-like receptor subfamily C, member 3 gene MP:0002160 abnormal reproductive system morphology IEA N RGD:5509061 20200514 MGI 1616804 Klrc3 killer cell lectin-like receptor subfamily C, member 3 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1616805 Lmbr1 limb region 1 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:11606546 1616805 Lmbr1 limb region 1 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11606546 1616805 Lmbr1 limb region 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:11606546 1616805 Lmbr1 limb region 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:11606546 1616805 Lmbr1 limb region 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11606546 1616805 Lmbr1 limb region 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1616805 Lmbr1 limb region 1 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:11606546 1616805 Lmbr1 limb region 1 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:11606546 1616805 Lmbr1 limb region 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11606546 1616807 Psg23 pregnancy-specific beta-1-glycoprotein 23 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14697515 1616809 Dnajb2 DnaJ heat shock protein family (Hsp40) member B2 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20210128 MGI 1616809 Dnajb2 DnaJ heat shock protein family (Hsp40) member B2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201231 MGI 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16462745 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20427744 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:16462745 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20427744 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16462745 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:20427744 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:16462745 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:20427744 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:20427744 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0003956 abnormal body size IAGP N RGD:5509061 20141003 MGI PMID:20427744 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:16462745 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:20427744 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21455290 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:20427744 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16462745 1616810 Gnasas1 GNAS antisense RNA 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20427744 1616811 Pcdh7 protocadherin 7 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20210114 MGI PMID:32635982 1616811 Pcdh7 protocadherin 7 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20210114 MGI PMID:32635982 1616811 Pcdh7 protocadherin 7 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20210114 MGI PMID:32635982 1616811 Pcdh7 protocadherin 7 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20210114 MGI PMID:32635982 1616811 Pcdh7 protocadherin 7 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20210114 MGI PMID:32635982 1616813 Islr immunoglobulin superfamily containing leucine-rich repeat gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20180322 MGI PMID:26924503 1616813 Islr immunoglobulin superfamily containing leucine-rich repeat gene MP:0004357 long tibia IAGP N RGD:5509061 20180322 MGI PMID:26924503 1616813 Islr immunoglobulin superfamily containing leucine-rich repeat gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180322 MGI PMID:26924503 1616813 Islr immunoglobulin superfamily containing leucine-rich repeat gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20180322 MGI PMID:26924503 1616813 Islr immunoglobulin superfamily containing leucine-rich repeat gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20180322 MGI PMID:26924503 1616813 Islr immunoglobulin superfamily containing leucine-rich repeat gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180322 MGI PMID:26924503 1616813 Islr immunoglobulin superfamily containing leucine-rich repeat gene MP:0008951 long radius IAGP N RGD:5509061 20180322 MGI PMID:26924503 1616813 Islr immunoglobulin superfamily containing leucine-rich repeat gene MP:0009709 hydrometra IEA N RGD:5509061 20230601 MGI 1616813 Islr immunoglobulin superfamily containing leucine-rich repeat gene MP:0010924 abnormal osteoid morphology IAGP N RGD:5509061 20180322 MGI PMID:26924503 1616813 Islr immunoglobulin superfamily containing leucine-rich repeat gene MP:0010926 increased osteoid volume IAGP N RGD:5509061 20180322 MGI PMID:26924503 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0003717 pallor IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0004085 abnormal heartbeat IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0011525 abnormal placenta intervillous maternal lacunae morphology IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0011526 abnormal placenta fetal blood space morphology IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0011527 disorganized placental labyrinth IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0012082 delayed heart development IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616816 Mecr mitochondrial trans-2-enoyl-CoA reductase gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20200310 MGI PMID:28369354 1616817 Eif2s3y eukaryotic translation initiation factor 2, subunit 3, structural gene Y-linked gene MP:0001925 male infertility IAGP N RGD:5509061 20180315 MGI PMID:25579647 1616817 Eif2s3y eukaryotic translation initiation factor 2, subunit 3, structural gene Y-linked gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20180315 MGI PMID:25579647 1616817 Eif2s3y eukaryotic translation initiation factor 2, subunit 3, structural gene Y-linked gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20180315 MGI PMID:25579647 1616817 Eif2s3y eukaryotic translation initiation factor 2, subunit 3, structural gene Y-linked gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180315 MGI PMID:25579647 1616817 Eif2s3y eukaryotic translation initiation factor 2, subunit 3, structural gene Y-linked gene MP:0005159 azoospermia IAGP N RGD:5509061 20180315 MGI PMID:25579647 1616817 Eif2s3y eukaryotic translation initiation factor 2, subunit 3, structural gene Y-linked gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20180315 MGI PMID:25579647 1616817 Eif2s3y eukaryotic translation initiation factor 2, subunit 3, structural gene Y-linked gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20180315 MGI PMID:25579647 1616820 Ddx3y DEAD box helicase 3, Y-linked gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20191219 MGI PMID:30613052 1616820 Ddx3y DEAD box helicase 3, Y-linked gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20191219 MGI PMID:30613052 1616822 Utp4 UTP4 small subunit processome component gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1616822 Utp4 UTP4 small subunit processome component gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20210128 MGI 1616822 Utp4 UTP4 small subunit processome component gene MP:0001284 absent vibrissae IEA N RGD:5509061 20210520 MGI 1616822 Utp4 UTP4 small subunit processome component gene MP:0001513 limb grasping IEA N RGD:5509061 20210128 MGI 1616822 Utp4 UTP4 small subunit processome component gene MP:0001523 impaired righting response IEA N RGD:5509061 20210128 MGI 1616822 Utp4 UTP4 small subunit processome component gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1616822 Utp4 UTP4 small subunit processome component gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240919 MGI 1616822 Utp4 UTP4 small subunit processome component gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20190502 MGI 1616822 Utp4 UTP4 small subunit processome component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616822 Utp4 UTP4 small subunit processome component gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20240919 MGI 1616822 Utp4 UTP4 small subunit processome component gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1616822 Utp4 UTP4 small subunit processome component gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241017 MGI 1616824 Terc telomerase RNA component gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20151126 MGI PMID:24626990 1616824 Terc telomerase RNA component gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0000066 osteoporosis IAGP N RGD:5509061 20151126 MGI PMID:24626990 1616824 Terc telomerase RNA component gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20151126 MGI PMID:24626990 1616824 Terc telomerase RNA component gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17360455 1616824 Terc telomerase RNA component gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0000175 absent bone marrow cell IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11809709 1616824 Terc telomerase RNA component gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23831727 1616824 Terc telomerase RNA component gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17360455 1616824 Terc telomerase RNA component gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:17360455 1616824 Terc telomerase RNA component gene MP:0000418 focal hair loss IAGP N RGD:5509061 20181220 MGI PMID:16142233 1616824 Terc telomerase RNA component gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:17360455 1616824 Terc telomerase RNA component gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:17785530 1616824 Terc telomerase RNA component gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10064584 1616824 Terc telomerase RNA component gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15084742 1616824 Terc telomerase RNA component gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17360455 1616824 Terc telomerase RNA component gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17360455 1616824 Terc telomerase RNA component gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20151126 MGI PMID:24626990 1616824 Terc telomerase RNA component gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15084742 1616824 Terc telomerase RNA component gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:10064584 1616824 Terc telomerase RNA component gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:15084742 1616824 Terc telomerase RNA component gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10064584 1616824 Terc telomerase RNA component gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17360455 1616824 Terc telomerase RNA component gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17360455 1616824 Terc telomerase RNA component gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17785530 1616824 Terc telomerase RNA component gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17785530 1616824 Terc telomerase RNA component gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:11809709 1616824 Terc telomerase RNA component gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17785530 1616824 Terc telomerase RNA component gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23831727 1616824 Terc telomerase RNA component gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:10064584 1616824 Terc telomerase RNA component gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20151126 MGI PMID:24626990 1616824 Terc telomerase RNA component gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:23831727 1616824 Terc telomerase RNA component gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:23831727 1616824 Terc telomerase RNA component gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:15731767 1616824 Terc telomerase RNA component gene MP:0002952 ventricular cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:23831727 1616824 Terc telomerase RNA component gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23831727 1616824 Terc telomerase RNA component gene MP:0003155 abnormal telomere length IAGP N RGD:5509061 20141003 MGI PMID:10654945 1616824 Terc telomerase RNA component gene MP:0003155 abnormal telomere length IAGP N RGD:5509061 20141003 MGI PMID:11809709 1616824 Terc telomerase RNA component gene MP:0003155 abnormal telomere length IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0003155 abnormal telomere length IAGP N RGD:5509061 20141003 MGI PMID:15084742 1616824 Terc telomerase RNA component gene MP:0003155 abnormal telomere length IAGP N RGD:5509061 20141003 MGI PMID:15731767 1616824 Terc telomerase RNA component gene MP:0003155 abnormal telomere length IAGP N RGD:5509061 20141003 MGI PMID:15893973 1616824 Terc telomerase RNA component gene MP:0003155 abnormal telomere length IAGP N RGD:5509061 20141003 MGI PMID:17360455 1616824 Terc telomerase RNA component gene MP:0003155 abnormal telomere length IAGP N RGD:5509061 20141003 MGI PMID:9335332 1616824 Terc telomerase RNA component gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0003199 calcified muscle IAGP N RGD:5509061 20170713 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:17360455 1616824 Terc telomerase RNA component gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23831727 1616824 Terc telomerase RNA component gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:15084742 1616824 Terc telomerase RNA component gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:15731767 1616824 Terc telomerase RNA component gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:24449270 1616824 Terc telomerase RNA component gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:17360455 1616824 Terc telomerase RNA component gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20151126 MGI PMID:24626990 1616824 Terc telomerase RNA component gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0003824 decreased left ventricle developed pressure IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0003853 dry skin IAGP N RGD:5509061 20181220 MGI PMID:16142233 1616824 Terc telomerase RNA component gene MP:0003916 decreased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:15084742 1616824 Terc telomerase RNA component gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15731767 1616824 Terc telomerase RNA component gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10654945 1616824 Terc telomerase RNA component gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10654945 1616824 Terc telomerase RNA component gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:15084742 1616824 Terc telomerase RNA component gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:15084742 1616824 Terc telomerase RNA component gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:23831727 1616824 Terc telomerase RNA component gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17785530 1616824 Terc telomerase RNA component gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17360455 1616824 Terc telomerase RNA component gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:12505991 1616824 Terc telomerase RNA component gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15084742 1616824 Terc telomerase RNA component gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:15893973 1616824 Terc telomerase RNA component gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:17785530 1616824 Terc telomerase RNA component gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20151126 MGI PMID:24626990 1616824 Terc telomerase RNA component gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:10654945 1616824 Terc telomerase RNA component gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10654945 1616824 Terc telomerase RNA component gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:17785530 1616824 Terc telomerase RNA component gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17785530 1616824 Terc telomerase RNA component gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17785530 1616824 Terc telomerase RNA component gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20151126 MGI PMID:24626990 1616824 Terc telomerase RNA component gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:23831727 1616824 Terc telomerase RNA component gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:23831727 1616824 Terc telomerase RNA component gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20151126 MGI PMID:24626990 1616824 Terc telomerase RNA component gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20151126 MGI PMID:24626990 1616824 Terc telomerase RNA component gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20151126 MGI PMID:24626990 1616824 Terc telomerase RNA component gene MP:0010924 abnormal osteoid morphology IAGP N RGD:5509061 20151126 MGI PMID:24626990 1616824 Terc telomerase RNA component gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20151126 MGI PMID:24626990 1616824 Terc telomerase RNA component gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18936156 1616824 Terc telomerase RNA component gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12944479 1616824 Terc telomerase RNA component gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10064584 1616824 Terc telomerase RNA component gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15084742 1616824 Terc telomerase RNA component gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:23831727 1616824 Terc telomerase RNA component gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:23831727 1616824 Terc telomerase RNA component gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20141003 MGI PMID:23831727 1616824 Terc telomerase RNA component gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20141003 MGI PMID:23831727 1616824 Terc telomerase RNA component gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17360455 1616824 Terc telomerase RNA component gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17785530 1616824 Terc telomerase RNA component gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:10064584 1616824 Terc telomerase RNA component gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20151126 MGI PMID:24626990 1616824 Terc telomerase RNA component gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:15084742 1616824 Terc telomerase RNA component gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:17360455 1616824 Terc telomerase RNA component gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:10654945 1616824 Terc telomerase RNA component gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:15235603 1616824 Terc telomerase RNA component gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:15731767 1616824 Terc telomerase RNA component gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:16142233 1616824 Terc telomerase RNA component gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:17785530 1616824 Terc telomerase RNA component gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:21145579 1616824 Terc telomerase RNA component gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:23831727 1616824 Terc telomerase RNA component gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:24449270 1616825 Slbp stem-loop binding protein gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1616825 Slbp stem-loop binding protein gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240523 MGI 1616825 Slbp stem-loop binding protein gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1616825 Slbp stem-loop binding protein gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1616825 Slbp stem-loop binding protein gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1616825 Slbp stem-loop binding protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1616825 Slbp stem-loop binding protein gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:11731796 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:11731796 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:12435627 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11731796 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:11731796 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11731796 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:11731796 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:12435627 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0004383 absent interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0004419 absent parietal bone IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0004447 small basioccipital bone IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11781823 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0006302 abnormal ectomesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20221215 MGI 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:11781823 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0012175 flat face IAGP N RGD:5509061 20171019 MGI PMID:9284043 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11781823 1616826 Ski ski sarcoma viral oncogene homolog (avian) gene MP:0030223 mandibular hyperostosis IAGP N RGD:5509061 20171019 MGI PMID:9284043 1616827 Sin3b transcriptional regulator, SIN3B (yeast) gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18332431 1616827 Sin3b transcriptional regulator, SIN3B (yeast) gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:18332431 1616827 Sin3b transcriptional regulator, SIN3B (yeast) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18332431 1616827 Sin3b transcriptional regulator, SIN3B (yeast) gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18332431 1616827 Sin3b transcriptional regulator, SIN3B (yeast) gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:18332431 1616827 Sin3b transcriptional regulator, SIN3B (yeast) gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18332431 1616827 Sin3b transcriptional regulator, SIN3B (yeast) gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:18332431 1616827 Sin3b transcriptional regulator, SIN3B (yeast) gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18332431 1616827 Sin3b transcriptional regulator, SIN3B (yeast) gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:18332431 1616827 Sin3b transcriptional regulator, SIN3B (yeast) gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18332431 1616827 Sin3b transcriptional regulator, SIN3B (yeast) gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:18332431 1616827 Sin3b transcriptional regulator, SIN3B (yeast) gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18332431 1616827 Sin3b transcriptional regulator, SIN3B (yeast) gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:18332431 1616827 Sin3b transcriptional regulator, SIN3B (yeast) gene MP:0010178 increased number of Howell-Jolly bodies IAGP N RGD:5509061 20141003 MGI PMID:18332431 1616827 Sin3b transcriptional regulator, SIN3B (yeast) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18332431 1616828 St6galnac4 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20231102 MGI PMID:37386100 1616828 St6galnac4 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 4 gene MP:0031051 lymph node hemorrhage IAGP N RGD:5509061 20231102 MGI PMID:37386100 1616832 Shcbp1 Shc SH2-domain binding protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:25153088 1616832 Shcbp1 Shc SH2-domain binding protein 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:25153088 1616832 Shcbp1 Shc SH2-domain binding protein 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:25153088 1616832 Shcbp1 Shc SH2-domain binding protein 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:25153088 1616832 Shcbp1 Shc SH2-domain binding protein 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:25153088 1616832 Shcbp1 Shc SH2-domain binding protein 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:25153088 1616834 Zfp106 zinc finger protein 106 gene MP:0000160 kyphosis IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20160804 MGI 1616834 Zfp106 zinc finger protein 106 gene MP:0000745 tremors IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20180426 MGI PMID:28072389 1616834 Zfp106 zinc finger protein 106 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20180426 MGI PMID:28072389 1616834 Zfp106 zinc finger protein 106 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20180426 MGI PMID:28072389 1616834 Zfp106 zinc finger protein 106 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0001021 small L4 dorsal root ganglion IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0001024 small L5 dorsal root ganglion IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20180426 MGI PMID:28072389 1616834 Zfp106 zinc finger protein 106 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1616834 Zfp106 zinc finger protein 106 gene MP:0001263 weight loss IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0001513 limb grasping IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20160804 MGI 1616834 Zfp106 zinc finger protein 106 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20180426 MGI PMID:28072389 1616834 Zfp106 zinc finger protein 106 gene MP:0002083 premature death IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0002183 gliosis IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0002883 chromatolysis IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20180426 MGI PMID:28072389 1616834 Zfp106 zinc finger protein 106 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0004262 abnormal physical strength IAGP N RGD:5509061 20180426 MGI PMID:28072389 1616834 Zfp106 zinc finger protein 106 gene MP:0005150 cachexia IAGP N RGD:5509061 20180426 MGI PMID:28072389 1616834 Zfp106 zinc finger protein 106 gene MP:0005356 positive geotaxis IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1616834 Zfp106 zinc finger protein 106 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0006404 abnormal lumbar dorsal root ganglion morphology IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0008918 microgliosis IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0009199 abnormal external male genitalia morphology IEA N RGD:5509061 20160804 MGI 1616834 Zfp106 zinc finger protein 106 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20180426 MGI PMID:28072389 1616834 Zfp106 zinc finger protein 106 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20180426 MGI PMID:28072389 1616834 Zfp106 zinc finger protein 106 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0009422 decreased gastrocnemius weight IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0009426 decreased soleus weight IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0009428 decreased tibialis anterior weight IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20180426 MGI PMID:28072389 1616834 Zfp106 zinc finger protein 106 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616834 Zfp106 zinc finger protein 106 gene MP:0013182 increased spinal cord apoptosis IAGP N RGD:5509061 20160721 MGI PMID:26604141 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20220811 MGI 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0000692 small spleen IEA N RGD:5509061 20201022 MGI 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20220616 MGI PMID:34343497 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20230629 MGI PMID:32800293 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20230629 MGI PMID:32800293 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11120814 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0005376 homeostasis/metabolism phenotype IAGP N RGD:5509061 20220616 MGI PMID:34343497 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20220616 MGI PMID:34343497 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20231207 MGI 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11120814 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22633459 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20230629 MGI PMID:32800293 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20230629 MGI PMID:32800293 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:11120814 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:10933401 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:10933401 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0008957 abnormal placenta junctional zone morphology IAGP N RGD:5509061 20230629 MGI PMID:32800293 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0008958 abnormal trophoblast glycogen cell morphology IAGP N RGD:5509061 20230629 MGI PMID:32800293 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0008959 abnormal spongiotrophoblast cell morphology IAGP N RGD:5509061 20230629 MGI PMID:32800293 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:10026221 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10933401 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0010768 mortality/aging IAGP N RGD:5509061 20220616 MGI PMID:34343497 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20230629 MGI PMID:32800293 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:10933401 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:21123651 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:10366581 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:8557029 1616839 Eif2ak2 eukaryotic translation initiation factor 2-alpha kinase 2 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:10933401 1616840 Myl4 myosin, light polypeptide 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160804 MGI 1616840 Myl4 myosin, light polypeptide 4 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1616840 Myl4 myosin, light polypeptide 4 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20160804 MGI 1616841 Myh8 myosin, heavy polypeptide 8, skeletal muscle, perinatal gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1616841 Myh8 myosin, heavy polypeptide 8, skeletal muscle, perinatal gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210826 MGI 1616841 Myh8 myosin, heavy polypeptide 8, skeletal muscle, perinatal gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210128 MGI 1616841 Myh8 myosin, heavy polypeptide 8, skeletal muscle, perinatal gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1616841 Myh8 myosin, heavy polypeptide 8, skeletal muscle, perinatal gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 1616841 Myh8 myosin, heavy polypeptide 8, skeletal muscle, perinatal gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:9382868 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:22199023 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9382868 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9382868 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22199023 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:22199023 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9382868 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11171584 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22199023 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:22199023 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:11150240 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:11171584 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:9382868 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:11171584 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:9382868 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:22199023 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:22199023 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:11171584 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:11171584 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:22199023 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:11171584 1616842 Myh4 myosin, heavy polypeptide 4, skeletal muscle gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:9382868 1616843 Myh2 myosin, heavy polypeptide 2, skeletal muscle, adult gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20240523 MGI 1616843 Myh2 myosin, heavy polypeptide 2, skeletal muscle, adult gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230119 MGI 1616844 Usp34 ubiquitin specific peptidase 34 gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20181129 MGI PMID:30181118 1616844 Usp34 ubiquitin specific peptidase 34 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20181129 MGI PMID:30181118 1616844 Usp34 ubiquitin specific peptidase 34 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20181129 MGI PMID:30181118 1616844 Usp34 ubiquitin specific peptidase 34 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20181129 MGI PMID:30181118 1616844 Usp34 ubiquitin specific peptidase 34 gene MP:0013616 decreased volumetric bone mineral density IAGP N RGD:5509061 20181129 MGI PMID:30181118 1616844 Usp34 ubiquitin specific peptidase 34 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20181129 MGI PMID:30181118 1616844 Usp34 ubiquitin specific peptidase 34 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20181129 MGI PMID:30181118 1616844 Usp34 ubiquitin specific peptidase 34 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20181129 MGI PMID:30181118 1616844 Usp34 ubiquitin specific peptidase 34 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20181129 MGI PMID:30181118 1616845 Commd1 COMM domain containing 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:17371845 1616845 Commd1 COMM domain containing 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17371845 1616845 Commd1 COMM domain containing 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17371845 1616845 Commd1 COMM domain containing 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:17371845 1616845 Commd1 COMM domain containing 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17371845 1616845 Commd1 COMM domain containing 1 gene MP:0003066 increased liver copper level IAGP N RGD:5509061 20141003 MGI PMID:22216203 1616845 Commd1 COMM domain containing 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:17371845 1616845 Commd1 COMM domain containing 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17371845 1616845 Commd1 COMM domain containing 1 gene MP:0004560 abnormal chorionic plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17371845 1616845 Commd1 COMM domain containing 1 gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:17371845 1616845 Commd1 COMM domain containing 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17371845 1616845 Commd1 COMM domain containing 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17371845 1616851 Mtx1 metaxin 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:7753840 1616851 Mtx1 metaxin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7753840 1616851 Mtx1 metaxin 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7753840 1616852 Klf12 Kruppel-like transcription factor 12 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210128 MGI 1616852 Klf12 Kruppel-like transcription factor 12 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20211021 MGI 1616852 Klf12 Kruppel-like transcription factor 12 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20201022 MGI 1616852 Klf12 Kruppel-like transcription factor 12 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20210128 MGI 1616853 Kcnu1 potassium channel, subfamily U, member 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20200310 MGI PMID:20138882 1616853 Kcnu1 potassium channel, subfamily U, member 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20200310 MGI PMID:21427226 1616853 Kcnu1 potassium channel, subfamily U, member 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20200310 MGI PMID:25675513 1616853 Kcnu1 potassium channel, subfamily U, member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:20138882 1616853 Kcnu1 potassium channel, subfamily U, member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:21427226 1616853 Kcnu1 potassium channel, subfamily U, member 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:21427226 1616853 Kcnu1 potassium channel, subfamily U, member 1 gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20200310 MGI PMID:20138882 1616853 Kcnu1 potassium channel, subfamily U, member 1 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20200310 MGI PMID:20138882 1616853 Kcnu1 potassium channel, subfamily U, member 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20200310 MGI PMID:21427226 1616853 Kcnu1 potassium channel, subfamily U, member 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20200310 MGI PMID:25675513 1616853 Kcnu1 potassium channel, subfamily U, member 1 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220714 MGI PMID:20138882 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22718760 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20220106 MGI PMID:31754024 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:22718760 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:10482234 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10482234 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11395002 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11988168 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:14766174 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22718760 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22794264 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:22718760 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20190808 MGI PMID:25639447 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:18305247 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:22423102 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:14766174 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:18305247 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:17901218 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:22794264 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:23263861 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20190808 MGI PMID:25639447 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20220106 MGI PMID:31754024 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10482234 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22423102 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22718760 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220106 MGI PMID:31754024 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22718760 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22718760 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190808 MGI PMID:25639447 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20190808 MGI PMID:25639447 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22718760 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20190808 MGI PMID:25639447 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:22423102 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:22794264 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:22423102 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20190808 MGI PMID:25639447 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20220106 MGI PMID:31754024 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22718760 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150402 MGI PMID:25136135 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:14766174 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:22423102 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:22718760 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20190808 MGI PMID:25639447 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20220106 MGI PMID:31754024 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20151112 MGI PMID:25496840 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20151112 MGI PMID:25496840 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20141003 MGI PMID:22423102 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0002946 delayed axon extension IAGP N RGD:5509061 20151112 MGI PMID:25496840 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:14766174 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:22423102 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:10471501 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:10471501 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:10471502 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22718760 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10471502 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:15836427 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:22423102 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:10471501 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:10471502 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0003952 abnormal copper level IAGP N RGD:5509061 20190808 MGI PMID:25639447 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:10471502 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20190808 MGI PMID:25639447 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:22718760 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:22423102 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:10471501 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:10471502 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0005218 abnormal pancreatic delta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10471502 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:22423102 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20190808 MGI PMID:25639447 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:10482234 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20220106 MGI PMID:31754024 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20220106 MGI PMID:31754024 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18842882 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20151112 MGI PMID:25496840 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:10471502 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0009181 decreased pancreatic delta cell number IAGP N RGD:5509061 20141003 MGI PMID:10471501 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:23263861 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20190808 MGI PMID:25639447 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:10482234 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22423102 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10471502 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10482234 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22794264 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17901218 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:22718760 1616862 Mnx1 motor neuron and pancreas homeobox 1 gene MP:0031330 delayed peripheral nervous system regeneration IAGP N RGD:5509061 20220106 MGI PMID:25496840 1616863 Foxf1 forkhead box F1 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11437453 1616863 Foxf1 forkhead box F1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:11943666 1616863 Foxf1 forkhead box F1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11437453 1616863 Foxf1 forkhead box F1 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0001263 weight loss IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:17881493 1616863 Foxf1 forkhead box F1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:17881493 1616863 Foxf1 forkhead box F1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11437453 1616863 Foxf1 forkhead box F1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11437453 1616863 Foxf1 forkhead box F1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0002726 abnormal pulmonary vein morphology IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0003159 abnormal esophageal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23946491 1616863 Foxf1 forkhead box F1 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20170629 MGI PMID:25091710 1616863 Foxf1 forkhead box F1 gene MP:0003250 absent gallbladder IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0003641 small lung IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0003794 delayed somite formation IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0004005 impaired contractility of intestinal smooth muscle IAGP N RGD:5509061 20141003 MGI PMID:23946491 1616863 Foxf1 forkhead box F1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11437453 1616863 Foxf1 forkhead box F1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11943666 1616863 Foxf1 forkhead box F1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0004548 dilated esophagus IAGP N RGD:5509061 20150319 MGI PMID:23946491 1616863 Foxf1 forkhead box F1 gene MP:0004559 small allantois IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:11437453 1616863 Foxf1 forkhead box F1 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0005084 abnormal gallbladder morphology IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20170629 MGI PMID:25091710 1616863 Foxf1 forkhead box F1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:11437453 1616863 Foxf1 forkhead box F1 gene MP:0006057 decreased vascular endothelial cell number IAGP N RGD:5509061 20170629 MGI PMID:25091710 1616863 Foxf1 forkhead box F1 gene MP:0006323 abnormal extraembryonic mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0008786 abnormal hindgut morphology IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0008802 abnormal intestinal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23946491 1616863 Foxf1 forkhead box F1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0009706 absent midgut IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:11437453 1616863 Foxf1 forkhead box F1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23946491 1616863 Foxf1 forkhead box F1 gene MP:0010906 abnormal lung bud morphology IAGP N RGD:5509061 20141003 MGI PMID:11943666 1616863 Foxf1 forkhead box F1 gene MP:0010977 fused right lung lobes IAGP N RGD:5509061 20141003 MGI PMID:11943666 1616863 Foxf1 forkhead box F1 gene MP:0010977 fused right lung lobes IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11943666 1616863 Foxf1 forkhead box F1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11437453 1616863 Foxf1 forkhead box F1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23946491 1616863 Foxf1 forkhead box F1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11437453 1616863 Foxf1 forkhead box F1 gene MP:0011140 decreased lung endothelial cell proliferation IAGP N RGD:5509061 20201119 MGI PMID:31199666 1616863 Foxf1 forkhead box F1 gene MP:0012740 abnormal posterior primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:11124112 1616863 Foxf1 forkhead box F1 gene MP:0020516 abnormal visceral yolk sac mesenchyme morphology IAGP N RGD:5509061 20180125 MGI PMID:17881493 1616865 Hells helicase, lymphoid specific gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 1616865 Hells helicase, lymphoid specific gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0000334 decreased granulocyte number IEA N RGD:5509061 20160804 MGI 1616865 Hells helicase, lymphoid specific gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:10781083 1616865 Hells helicase, lymphoid specific gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:10781083 1616865 Hells helicase, lymphoid specific gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11325543 1616865 Hells helicase, lymphoid specific gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0001925 male infertility IAGP N RGD:5509061 20200227 MGI PMID:32001511 1616865 Hells helicase, lymphoid specific gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20200227 MGI PMID:32001511 1616865 Hells helicase, lymphoid specific gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11325543 1616865 Hells helicase, lymphoid specific gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1616865 Hells helicase, lymphoid specific gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:11325543 1616865 Hells helicase, lymphoid specific gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20211021 MGI 1616865 Hells helicase, lymphoid specific gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:15647320 1616865 Hells helicase, lymphoid specific gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:11711429 1616865 Hells helicase, lymphoid specific gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11325543 1616865 Hells helicase, lymphoid specific gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:11325543 1616865 Hells helicase, lymphoid specific gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11325543 1616865 Hells helicase, lymphoid specific gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200227 MGI PMID:32001511 1616865 Hells helicase, lymphoid specific gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200227 MGI PMID:32001511 1616865 Hells helicase, lymphoid specific gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10781083 1616865 Hells helicase, lymphoid specific gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:10781083 1616865 Hells helicase, lymphoid specific gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1616865 Hells helicase, lymphoid specific gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 1616865 Hells helicase, lymphoid specific gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10781083 1616865 Hells helicase, lymphoid specific gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20200227 MGI PMID:32001511 1616865 Hells helicase, lymphoid specific gene MP:0008495 decreased IgG1 level IEA N RGD:5509061 20160804 MGI 1616865 Hells helicase, lymphoid specific gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20200227 MGI PMID:32001511 1616865 Hells helicase, lymphoid specific gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20200227 MGI PMID:32001511 1616865 Hells helicase, lymphoid specific gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11325543 1616865 Hells helicase, lymphoid specific gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15105378 1616865 Hells helicase, lymphoid specific gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1616865 Hells helicase, lymphoid specific gene MP:0011951 increased cardiac stroke volume IEA N RGD:5509061 20211021 MGI 1616865 Hells helicase, lymphoid specific gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20200227 MGI PMID:32001511 1616867 Esx1 extraembryonic, spermatogenesis, homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9806555 1616867 Esx1 extraembryonic, spermatogenesis, homeobox 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:9806555 1616867 Esx1 extraembryonic, spermatogenesis, homeobox 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:9806555 1616867 Esx1 extraembryonic, spermatogenesis, homeobox 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9806555 1616867 Esx1 extraembryonic, spermatogenesis, homeobox 1 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9806555 1616867 Esx1 extraembryonic, spermatogenesis, homeobox 1 gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:9806555 1616867 Esx1 extraembryonic, spermatogenesis, homeobox 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9806555 1616867 Esx1 extraembryonic, spermatogenesis, homeobox 1 gene MP:0011531 abnormal syncytiotrophoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:9806555 1616867 Esx1 extraembryonic, spermatogenesis, homeobox 1 gene MP:0012108 increased trophoblast glycogen cell number IAGP N RGD:5509061 20141003 MGI PMID:9806555 1616868 Ces3b carboxylesterase 3B gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20220811 MGI 1616869 Chl1 cell adhesion molecule L1-like gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12391163 1616869 Chl1 cell adhesion molecule L1-like gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:12391163 1616869 Chl1 cell adhesion molecule L1-like gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:19074023 1616869 Chl1 cell adhesion molecule L1-like gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20240523 MGI PMID:25007825 1616869 Chl1 cell adhesion molecule L1-like gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12391163 1616869 Chl1 cell adhesion molecule L1-like gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:19074023 1616869 Chl1 cell adhesion molecule L1-like gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20141003 MGI PMID:18447583 1616869 Chl1 cell adhesion molecule L1-like gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18447583 1616869 Chl1 cell adhesion molecule L1-like gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:18447583 1616869 Chl1 cell adhesion molecule L1-like gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:18447583 1616869 Chl1 cell adhesion molecule L1-like gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12391163 1616869 Chl1 cell adhesion molecule L1-like gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:19074023 1616869 Chl1 cell adhesion molecule L1-like gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:12391163 1616869 Chl1 cell adhesion molecule L1-like gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:18447583 1616869 Chl1 cell adhesion molecule L1-like gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18046458 1616869 Chl1 cell adhesion molecule L1-like gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12391163 1616871 Ces1g carboxylesterase 1G gene MP:0001260 increased body weight IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0001261 obese IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0001399 hyperactivity IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0003103 liver degeneration IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0005283 increased unsaturated fatty acids level IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0005286 decreased saturated fatty acids level IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0010331 abnormal apolipoprotein level IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0010332 abnormal circulating apolipoprotein level IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0010333 abnormal circulating apolipoprotein E level IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0014145 increased white adipose tissue mass IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616871 Ces1g carboxylesterase 1G gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20180809 MGI PMID:22806626 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:19494204 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:19494204 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:19494204 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20180614 MGI PMID:24712709 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0003011 delayed dark adaptation IAGP N RGD:5509061 20141003 MGI PMID:10412977 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:10412977 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19494204 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19494204 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20160407 MGI PMID:25712131 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20160114 MGI 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:19494204 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10412977 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18515570 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19494204 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20180614 MGI PMID:29145636 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:10412977 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:19494204 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:10412977 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:17032653 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20180614 MGI PMID:29145636 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0005546 choroidal neovascularization IAGP N RGD:5509061 20220217 MGI PMID:19494204 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19494204 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0006187 retina deposits IAGP N RGD:5509061 20141003 MGI PMID:19494204 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:19494204 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:10412977 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:18515570 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:19494204 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:18515570 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20160407 MGI PMID:25712131 1616873 Abca4 ATP-binding cassette, sub-family A member 4 gene MP:0011232 abnormal vitamin A level IAGP N RGD:5509061 20141003 MGI PMID:18515570 1617018 Sec14l5 SEC14-like lipid binding 5 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20220811 MGI 1617061 Phf11c PHD finger protein 11C gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1617091 Prlh prolactin releasing hormone gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617091 Prlh prolactin releasing hormone gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617091 Prlh prolactin releasing hormone gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617091 Prlh prolactin releasing hormone gene MP:0001260 increased body weight IAGP N RGD:5509061 20150514 MGI PMID:25176149 1617091 Prlh prolactin releasing hormone gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617091 Prlh prolactin releasing hormone gene MP:0001261 obese IAGP N RGD:5509061 20150514 MGI PMID:25176149 1617091 Prlh prolactin releasing hormone gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617091 Prlh prolactin releasing hormone gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20150514 MGI PMID:25176149 1617091 Prlh prolactin releasing hormone gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20150514 MGI PMID:25176149 1617091 Prlh prolactin releasing hormone gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617091 Prlh prolactin releasing hormone gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20150514 MGI PMID:25176149 1617091 Prlh prolactin releasing hormone gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617091 Prlh prolactin releasing hormone gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20150514 MGI PMID:25176149 1617091 Prlh prolactin releasing hormone gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20150514 MGI PMID:25176149 1617091 Prlh prolactin releasing hormone gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20150514 MGI PMID:25176149 1617091 Prlh prolactin releasing hormone gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617091 Prlh prolactin releasing hormone gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617091 Prlh prolactin releasing hormone gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617091 Prlh prolactin releasing hormone gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20150514 MGI PMID:25176149 1617091 Prlh prolactin releasing hormone gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617091 Prlh prolactin releasing hormone gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20150514 MGI PMID:25176149 1617091 Prlh prolactin releasing hormone gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617091 Prlh prolactin releasing hormone gene MP:0006276 abnormal autonomic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617091 Prlh prolactin releasing hormone gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20150514 MGI PMID:25176149 1617091 Prlh prolactin releasing hormone gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617091 Prlh prolactin releasing hormone gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20150514 MGI PMID:25176149 1617091 Prlh prolactin releasing hormone gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20150514 MGI PMID:25176149 1617091 Prlh prolactin releasing hormone gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20150514 MGI PMID:25176149 1617091 Prlh prolactin releasing hormone gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617091 Prlh prolactin releasing hormone gene MP:0011939 increased food intake IAGP N RGD:5509061 20150514 MGI PMID:25176149 1617091 Prlh prolactin releasing hormone gene MP:0011958 increased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:19033670 1617113 Vmn2r116 vomeronasal 2, receptor 116 gene MP:0002243 abnormal vomeronasal organ morphology IAGP N RGD:5509061 20210225 MGI PMID:30367054 1617113 Vmn2r116 vomeronasal 2, receptor 116 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:20596023 1617113 Vmn2r116 vomeronasal 2, receptor 116 gene MP:0013596 abnormal vomeronasal organ physiology IAGP N RGD:5509061 20210225 MGI PMID:30367054 1617115 Klf14 Kruppel-like transcription factor 14 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20170413 MGI PMID:26368306 1617115 Klf14 Kruppel-like transcription factor 14 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20170907 MGI PMID:26439168 1617115 Klf14 Kruppel-like transcription factor 14 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20170907 MGI PMID:26439168 1617115 Klf14 Kruppel-like transcription factor 14 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220519 MGI 1617115 Klf14 Kruppel-like transcription factor 14 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1617115 Klf14 Kruppel-like transcription factor 14 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20170907 MGI PMID:26439168 1617115 Klf14 Kruppel-like transcription factor 14 gene MP:0004025 polyploidy IAGP N RGD:5509061 20170907 MGI PMID:26439168 1617115 Klf14 Kruppel-like transcription factor 14 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20170907 MGI PMID:26439168 1617115 Klf14 Kruppel-like transcription factor 14 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20170907 MGI PMID:26439168 1617115 Klf14 Kruppel-like transcription factor 14 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 1617115 Klf14 Kruppel-like transcription factor 14 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20170907 MGI PMID:26439168 1617115 Klf14 Kruppel-like transcription factor 14 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20220811 MGI 1617115 Klf14 Kruppel-like transcription factor 14 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20170907 MGI PMID:26439168 1617115 Klf14 Kruppel-like transcription factor 14 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:26439168 1617144 Ccin calicin gene MP:0001925 male infertility IAGP N RGD:5509061 20220811 MGI PMID:35793634 1617144 Ccin calicin gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220811 MGI PMID:35793634 1617144 Ccin calicin gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220811 MGI PMID:35793634 1617144 Ccin calicin gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220811 MGI PMID:35793634 1617144 Ccin calicin gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220811 MGI PMID:35793634 1617144 Ccin calicin gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220811 MGI PMID:35793634 1617145 Rab44 RAB44, member RAS oncogene family gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20210513 MGI PMID:32238914 1617145 Rab44 RAB44, member RAS oncogene family gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20210513 MGI PMID:32238914 1617145 Rab44 RAB44, member RAS oncogene family gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20210513 MGI PMID:32238914 1617145 Rab44 RAB44, member RAS oncogene family gene MP:0030759 decreased circulating histamine level IAGP N RGD:5509061 20210513 MGI PMID:32238914 1617148 Arhgef15 Rho guanine nucleotide exchange factor 15 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:22535667 1617148 Arhgef15 Rho guanine nucleotide exchange factor 15 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20181227 MGI 1617148 Arhgef15 Rho guanine nucleotide exchange factor 15 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1617148 Arhgef15 Rho guanine nucleotide exchange factor 15 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20181227 MGI 1617148 Arhgef15 Rho guanine nucleotide exchange factor 15 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22535667 1617148 Arhgef15 Rho guanine nucleotide exchange factor 15 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23029280 1617148 Arhgef15 Rho guanine nucleotide exchange factor 15 gene MP:0003402 decreased liver weight IEA N RGD:5509061 20220519 MGI 1617148 Arhgef15 Rho guanine nucleotide exchange factor 15 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:21029865 1617148 Arhgef15 Rho guanine nucleotide exchange factor 15 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1617148 Arhgef15 Rho guanine nucleotide exchange factor 15 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1617153 Pramel31 PRAME like 31 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1617155 Trim63 tripartite motif-containing 63 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200827 MGI PMID:23512667 1617155 Trim63 tripartite motif-containing 63 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17272810 1617155 Trim63 tripartite motif-containing 63 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20200827 MGI PMID:23512667 1617155 Trim63 tripartite motif-containing 63 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0002083 premature death IAGP N RGD:5509061 20200827 MGI PMID:23512667 1617155 Trim63 tripartite motif-containing 63 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17272810 1617155 Trim63 tripartite motif-containing 63 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200827 MGI PMID:23512667 1617155 Trim63 tripartite motif-containing 63 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20200827 MGI PMID:23512667 1617155 Trim63 tripartite motif-containing 63 gene MP:0004064 decreased susceptibility to induced muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:11679633 1617155 Trim63 tripartite motif-containing 63 gene MP:0004064 decreased susceptibility to induced muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:19506036 1617155 Trim63 tripartite motif-containing 63 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20200827 MGI PMID:23512667 1617155 Trim63 tripartite motif-containing 63 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20200827 MGI PMID:23512667 1617155 Trim63 tripartite motif-containing 63 gene MP:0004094 abnormal M line morphology IAGP N RGD:5509061 20200827 MGI PMID:23512667 1617155 Trim63 tripartite motif-containing 63 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20200827 MGI PMID:23512667 1617155 Trim63 tripartite motif-containing 63 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20200827 MGI PMID:23512667 1617155 Trim63 tripartite motif-containing 63 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0010226 increased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200827 MGI PMID:23512667 1617155 Trim63 tripartite motif-containing 63 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200827 MGI PMID:23512667 1617155 Trim63 tripartite motif-containing 63 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20200827 MGI PMID:23512667 1617155 Trim63 tripartite motif-containing 63 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:18157088 1617155 Trim63 tripartite motif-containing 63 gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20161124 MGI PMID:18157088 1617160 Ncbp1 nuclear cap binding protein subunit 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20201022 MGI 1617160 Ncbp1 nuclear cap binding protein subunit 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20161222 MGI PMID:26857995 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000160 kyphosis IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000160 kyphosis IAGP N RGD:5509061 20161222 MGI PMID:26857995 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20161222 MGI PMID:26857995 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20161222 MGI PMID:26857995 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000447 flattened snout IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210520 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20161222 MGI PMID:26857995 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000774 decreased brain size IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0000921 demyelination IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001169 abnormal bulbourethral gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001200 thick skin IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001258 decreased body length IAGP N RGD:5509061 20161222 MGI PMID:26857995 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161222 MGI PMID:26857995 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001265 decreased body size IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001265 decreased body size IAGP N RGD:5509061 20161222 MGI PMID:26857995 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001393 ataxia IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001513 limb grasping IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20210128 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230601 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20161222 MGI PMID:26857995 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001847 brain inflammation IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0002083 premature death IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0002691 small stomach IEA N RGD:5509061 20210520 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0003174 increased lysosomal enzyme secretion IAGP N RGD:5509061 20161222 MGI PMID:26857995 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210826 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0003354 astrocytosis IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0003652 abnormal skin turgor IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20161222 MGI PMID:26857995 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20210826 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210826 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20161222 MGI PMID:26857995 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20150312 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17652091 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:20472886 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0006162 thick eyelids IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20161222 MGI PMID:26857995 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0009105 penis prolapse IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0009160 abnormal pancreatic acinar cell zymogen granule morphology IAGP N RGD:5509061 20141003 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0009978 abnormal cerebellum white matter morphology IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20161222 MGI PMID:26857995 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:24127423 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0012506 brain atrophy IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0013159 Purkinje cell axonal dystrophy IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0013558 abnormal exocrine gland morphology IAGP N RGD:5509061 20150312 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0013582 abnormal lateral nasal gland morphology IAGP N RGD:5509061 20150312 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0013594 abnormal parotid gland acinus morphology IAGP N RGD:5509061 20150312 MGI PMID:17962477 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0014114 abnormal cognition IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20160922 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0030035 small nasal bridge IAGP N RGD:5509061 20170914 MGI PMID:25107912 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0030074 coarse facial features IAGP N RGD:5509061 20170921 MGI PMID:26857995 1617164 Gnptab N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits gene MP:0031074 increased circulating type I collagen C-terminal telopeptide level IAGP N RGD:5509061 20200618 MGI PMID:24127423 1617167 Tmprss9 transmembrane protease, serine 9 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200402 MGI PMID:31943016 1617167 Tmprss9 transmembrane protease, serine 9 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20200402 MGI PMID:31943016 1617167 Tmprss9 transmembrane protease, serine 9 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20200402 MGI PMID:31943016 1617167 Tmprss9 transmembrane protease, serine 9 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20200402 MGI PMID:31943016 1617167 Tmprss9 transmembrane protease, serine 9 gene MP:0020396 abnormal social recognition IAGP N RGD:5509061 20200402 MGI PMID:31943016 1617174 Akap7 A kinase anchor protein 7 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20201022 MGI 1617174 Akap7 A kinase anchor protein 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23035250 1617178 Ndufa4l2 Ndufa4, mitochondrial complex associated like 2 gene MP:0031252 abnormal physiological response to hypoxia IAGP N RGD:5509061 20210729 MGI PMID:31848220 1617180 Tsbp1 testis expressed basic protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1617181 Taf9b TATA-box binding protein associated factor 9B gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1617181 Taf9b TATA-box binding protein associated factor 9B gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1617181 Taf9b TATA-box binding protein associated factor 9B gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1617182 Zfp174 zinc finger protein 174 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1617182 Zfp174 zinc finger protein 174 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1617182 Zfp174 zinc finger protein 174 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20240523 MGI 1617182 Zfp174 zinc finger protein 174 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20221215 MGI 1617182 Zfp174 zinc finger protein 174 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1617182 Zfp174 zinc finger protein 174 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200402 MGI 1617183 Lca5l Leber congenital amaurosis 5-like gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20231207 MGI 1617183 Lca5l Leber congenital amaurosis 5-like gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1617183 Lca5l Leber congenital amaurosis 5-like gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1617183 Lca5l Leber congenital amaurosis 5-like gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1617183 Lca5l Leber congenital amaurosis 5-like gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20200514 MGI 1617183 Lca5l Leber congenital amaurosis 5-like gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1617183 Lca5l Leber congenital amaurosis 5-like gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20210128 MGI 1617183 Lca5l Leber congenital amaurosis 5-like gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20211021 MGI 1617185 Kng2 kininogen 2 gene MP:0001257 increased body length IEA N RGD:5509061 20160804 MGI 1617185 Kng2 kininogen 2 gene MP:0001413 abnormal response to new environment IEA N RGD:5509061 20191128 MGI 1617185 Kng2 kininogen 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1617190 Trim56 tripartite motif-containing 56 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1617190 Trim56 tripartite motif-containing 56 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1617190 Trim56 tripartite motif-containing 56 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20211021 MGI 1617190 Trim56 tripartite motif-containing 56 gene MP:0004974 decreased regulatory T cell number IEA N RGD:5509061 20201022 MGI 1617190 Trim56 tripartite motif-containing 56 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1617190 Trim56 tripartite motif-containing 56 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1617190 Trim56 tripartite motif-containing 56 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20211021 MGI 1617190 Trim56 tripartite motif-containing 56 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0001147 small testis IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0001935 decreased litter size IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617195 4930590J08Rik RIKEN cDNA 4930590J08 gene gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20230406 MGI PMID:36331537 1617198 Wee2 WEE1 homolog 2 (S. pombe) gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1617198 Wee2 WEE1 homolog 2 (S. pombe) gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1617198 Wee2 WEE1 homolog 2 (S. pombe) gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1617198 Wee2 WEE1 homolog 2 (S. pombe) gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20231109 MGI PMID:37527245 1617198 Wee2 WEE1 homolog 2 (S. pombe) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20231109 MGI PMID:37527245 1617198 Wee2 WEE1 homolog 2 (S. pombe) gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220811 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0000644 dextrocardia IEA N RGD:5509061 20141003 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0000690 absent spleen IEA N RGD:5509061 20141218 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0002639 micrognathia IEA N RGD:5509061 20141218 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0003178 left pulmonary isomerism IEA N RGD:5509061 20141218 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0004113 abnormal aortic arch morphology IEA N RGD:5509061 20141218 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0004157 interrupted aortic arch IEA N RGD:5509061 20141218 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20141003 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0009241 thick sperm flagellum IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141218 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0010403 atrial septal defect IEA N RGD:5509061 20141003 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0010439 abnormal hepatic vein morphology IEA N RGD:5509061 20141003 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0011249 abdominal situs inversus IEA N RGD:5509061 20141003 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0011250 abdominal situs ambiguus IEA N RGD:5509061 20141218 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0011252 situs inversus totalis IEA N RGD:5509061 20141003 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0011253 situs inversus with levocardia IEA N RGD:5509061 20141003 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0011569 abnormal azygos vein morphology IEA N RGD:5509061 20141003 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0011659 interrupted aortic arch, type b IEA N RGD:5509061 20141218 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20141003 MGI 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220721 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0031438 abnormal sperm radial spoke morphology IAGP N RGD:5509061 20220915 MGI PMID:34169321 1617201 Drc1 dynein regulatory complex subunit 1 gene MP:0031515 l-loop transposition of the great arteries IEA N RGD:5509061 20240118 MGI 1617203 Pttg1ip2 PTTG1IP family member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1617206 Txlng taxilin gamma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141218 MGI PMID:24440290 1617206 Txlng taxilin gamma gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141218 MGI PMID:24440290 1617207 Slc2a12 solute carrier family 2 (facilitated glucose transporter), member 12 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20220519 MGI 1617207 Slc2a12 solute carrier family 2 (facilitated glucose transporter), member 12 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20201022 MGI 1617210 Tas2r139 taste receptor, type 2, member 139 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 1617210 Tas2r139 taste receptor, type 2, member 139 gene MP:0000692 small spleen IEA N RGD:5509061 20181227 MGI 1617210 Tas2r139 taste receptor, type 2, member 139 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20181227 MGI 1617210 Tas2r139 taste receptor, type 2, member 139 gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 1617210 Tas2r139 taste receptor, type 2, member 139 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1617212 Gm5134 predicted gene 5134 gene MP:0001413 abnormal response to new environment IEA N RGD:5509061 20141003 MGI 1617212 Gm5134 predicted gene 5134 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20141003 MGI 1617212 Gm5134 predicted gene 5134 gene MP:0005266 abnormal metabolism IEA N RGD:5509061 20160804 MGI 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21930934 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:15661756 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0000410 waved hair IAGP N RGD:5509061 20190711 MGI PMID:28069640 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0000416 sparse hair IAGP N RGD:5509061 20190711 MGI PMID:28069640 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21930934 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:21930934 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21930934 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15661756 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15661756 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20190711 MGI PMID:28069640 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001853 heart inflammation IAGP N RGD:5509061 20190711 MGI PMID:28069640 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001922 reduced male fertility IEA N RGD:5509061 20111116 MGI 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0001926 female infertility IEA N RGD:5509061 20111116 MGI 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0002001 blindness IAGP N RGD:5509061 20190711 MGI PMID:28069640 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0002083 premature death IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:21930934 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15661756 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15661756 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20190711 MGI PMID:28069640 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0002952 ventricular cardiomyopathy IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:21930934 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15661756 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0005330 cardiomyopathy IEA N RGD:5509061 20111116 MGI 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:15661756 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0006138 congestive heart failure IEA N RGD:5509061 20111116 MGI 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0006236 absent Meibomian glands IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21930934 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:15661756 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0009351 thin hair shaft IAGP N RGD:5509061 20141003 MGI PMID:15661756 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0009416 cardiac muscle degeneration IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21930934 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15661756 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141003 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:21930934 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0013744 abnormal conjunctival sac morphology IAGP N RGD:5509061 20150416 MGI PMID:22928477 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20171012 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0021160 decreased heart right ventricle wall thickness IAGP N RGD:5509061 20231221 MGI PMID:25691752 1617213 Ppp1r13l protein phosphatase 1, regulatory subunit 13 like gene MP:0031157 abnormal arterial thrombosis IAGP N RGD:5509061 20201224 MGI PMID:15661756 1617214 Mamld1 mastermind-like domain containing 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1617214 Mamld1 mastermind-like domain containing 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1617214 Mamld1 mastermind-like domain containing 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1617214 Mamld1 mastermind-like domain containing 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1617214 Mamld1 mastermind-like domain containing 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1617214 Mamld1 mastermind-like domain containing 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20220811 MGI 1617214 Mamld1 mastermind-like domain containing 1 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20201231 MGI 1617214 Mamld1 mastermind-like domain containing 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1617214 Mamld1 mastermind-like domain containing 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1617214 Mamld1 mastermind-like domain containing 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1617214 Mamld1 mastermind-like domain containing 1 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20210128 MGI 1617215 Frmpd4 FERM and PDZ domain containing 4 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:22561452 1617215 Frmpd4 FERM and PDZ domain containing 4 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22561452 1617215 Frmpd4 FERM and PDZ domain containing 4 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:22561452 1617216 Grxcr2 glutaredoxin, cysteine rich 2 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20201119 MGI PMID:30157177 1617216 Grxcr2 glutaredoxin, cysteine rich 2 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20201119 MGI PMID:30157177 1617216 Grxcr2 glutaredoxin, cysteine rich 2 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20201119 MGI PMID:30157177 1617216 Grxcr2 glutaredoxin, cysteine rich 2 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20201119 MGI PMID:30157177 1617216 Grxcr2 glutaredoxin, cysteine rich 2 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20201119 MGI PMID:30157177 1617216 Grxcr2 glutaredoxin, cysteine rich 2 gene MP:0004814 reduced linear vestibular evoked potential IAGP N RGD:5509061 20201119 MGI PMID:30157177 1617216 Grxcr2 glutaredoxin, cysteine rich 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20150528 MGI PMID:24619944 1617216 Grxcr2 glutaredoxin, cysteine rich 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20201119 MGI PMID:30157177 1617216 Grxcr2 glutaredoxin, cysteine rich 2 gene MP:0011062 abnormal outer hair cell kinocilium morphology IAGP N RGD:5509061 20201119 MGI PMID:30157177 1617216 Grxcr2 glutaredoxin, cysteine rich 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20201119 MGI PMID:30157177 1617218 Tgm4 transglutaminase 4 (prostate) gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:23341775 1617218 Tgm4 transglutaminase 4 (prostate) gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:23341775 1617218 Tgm4 transglutaminase 4 (prostate) gene MP:0030983 failure of copulatory plug deposition IAGP N RGD:5509061 20191017 MGI PMID:23341775 1617219 Gmppb GDP-mannose pyrophosphorylase B gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20240321 MGI PMID:38419795 1617223 Tafa3 TAFA chemokine like family member 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20180719 MGI PMID:29184127 1617223 Tafa3 TAFA chemokine like family member 3 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20180719 MGI PMID:29184127 1617223 Tafa3 TAFA chemokine like family member 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20180719 MGI PMID:29184127 1617223 Tafa3 TAFA chemokine like family member 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1617223 Tafa3 TAFA chemokine like family member 3 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20180719 MGI PMID:29184127 1617223 Tafa3 TAFA chemokine like family member 3 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201022 MGI 1617223 Tafa3 TAFA chemokine like family member 3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20190502 MGI 1617223 Tafa3 TAFA chemokine like family member 3 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20180719 MGI PMID:29184127 1617223 Tafa3 TAFA chemokine like family member 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:29184127 1617224 Dcst2 DC-STAMP domain containing 2 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20210520 MGI PMID:33871360 1617224 Dcst2 DC-STAMP domain containing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20210520 MGI PMID:33871360 1617228 Dnai7 dynein axonemal intermediate chain 7 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16862160 1617228 Dnai7 dynein axonemal intermediate chain 7 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16862160 1617228 Dnai7 dynein axonemal intermediate chain 7 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16862160 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20160915 MGI PMID:22227195 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:22227195 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22227195 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22227195 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:23864655 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:22227195 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23864655 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23864655 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:22227195 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23864655 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22227195 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22227195 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22227195 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22227195 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23864655 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:23864655 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22227195 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:23864655 1617229 Pgap3 post-GPI attachment to proteins 3 gene MP:0011496 abnormal head size IAGP N RGD:5509061 20141003 MGI PMID:22227195 1617231 Ocrl OCRL, inositol polyphosphate-5-phosphatase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21183592 1617231 Ocrl OCRL, inositol polyphosphate-5-phosphatase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21183592 1617231 Ocrl OCRL, inositol polyphosphate-5-phosphatase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21183592 1617231 Ocrl OCRL, inositol polyphosphate-5-phosphatase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9593760 1617231 Ocrl OCRL, inositol polyphosphate-5-phosphatase gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:21183592 1617231 Ocrl OCRL, inositol polyphosphate-5-phosphatase gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:21183592 1617231 Ocrl OCRL, inositol polyphosphate-5-phosphatase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9593760 1617231 Ocrl OCRL, inositol polyphosphate-5-phosphatase gene MP:0011555 increased urine microglobulin level IAGP N RGD:5509061 20141003 MGI PMID:21183592 1617233 Dop1a DOP1 leucine zipper like protein A gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20220519 MGI 1617233 Dop1a DOP1 leucine zipper like protein A gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1617233 Dop1a DOP1 leucine zipper like protein A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1617233 Dop1a DOP1 leucine zipper like protein A gene MP:0002637 small uterus IEA N RGD:5509061 20220519 MGI 1617233 Dop1a DOP1 leucine zipper like protein A gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1617234 Strip2 striatin interacting protein 2 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20200514 MGI 1617234 Strip2 striatin interacting protein 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20200514 MGI 1617234 Strip2 striatin interacting protein 2 gene MP:0003450 enlarged pancreas IEA N RGD:5509061 20200514 MGI 1617234 Strip2 striatin interacting protein 2 gene MP:0003900 shortened QT interval IAGP N RGD:5509061 20210916 MGI PMID:27122098 1617234 Strip2 striatin interacting protein 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20210916 MGI PMID:27122098 1617234 Strip2 striatin interacting protein 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210916 MGI PMID:27122098 1617241 Spata31f3 spermatogenesis associated 31 subfamily F member 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230720 MGI 1617241 Spata31f3 spermatogenesis associated 31 subfamily F member 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230720 MGI 1617241 Spata31f3 spermatogenesis associated 31 subfamily F member 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230720 MGI 1617241 Spata31f3 spermatogenesis associated 31 subfamily F member 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230720 MGI 1617241 Spata31f3 spermatogenesis associated 31 subfamily F member 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230720 MGI 1617241 Spata31f3 spermatogenesis associated 31 subfamily F member 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230720 MGI 1617241 Spata31f3 spermatogenesis associated 31 subfamily F member 3 gene MP:0001147 small testis IEA N RGD:5509061 20230720 MGI 1617241 Spata31f3 spermatogenesis associated 31 subfamily F member 3 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230720 MGI 1617241 Spata31f3 spermatogenesis associated 31 subfamily F member 3 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230720 MGI 1617241 Spata31f3 spermatogenesis associated 31 subfamily F member 3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20230720 MGI 1617241 Spata31f3 spermatogenesis associated 31 subfamily F member 3 gene MP:0013436 increased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20230720 MGI 1617244 Tango6 transport and golgi organization 6 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20160811 MGI 1617244 Tango6 transport and golgi organization 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1617244 Tango6 transport and golgi organization 6 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1617245 Rp1l1 retinitis pigmentosa 1 homolog like 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:19657028 1617245 Rp1l1 retinitis pigmentosa 1 homolog like 1 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:19657028 1617245 Rp1l1 retinitis pigmentosa 1 homolog like 1 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:19657028 1617245 Rp1l1 retinitis pigmentosa 1 homolog like 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19657028 1617245 Rp1l1 retinitis pigmentosa 1 homolog like 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19657028 1617245 Rp1l1 retinitis pigmentosa 1 homolog like 1 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19657028 1617245 Rp1l1 retinitis pigmentosa 1 homolog like 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:19657028 1617245 Rp1l1 retinitis pigmentosa 1 homolog like 1 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:19657028 1617247 Nup98 nucleoporin 98 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:11248054 1617247 Nup98 nucleoporin 98 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20200310 MGI PMID:11248054 1617247 Nup98 nucleoporin 98 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:11248054 1617247 Nup98 nucleoporin 98 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20200310 MGI PMID:16546098 1617247 Nup98 nucleoporin 98 gene MP:0001839 abnormal level of surface class I molecules IAGP N RGD:5509061 20200310 MGI PMID:16546098 1617247 Nup98 nucleoporin 98 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20200310 MGI PMID:26731471 1617247 Nup98 nucleoporin 98 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200310 MGI PMID:26731471 1617247 Nup98 nucleoporin 98 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:16546098 1617247 Nup98 nucleoporin 98 gene MP:0005040 abnormal MHC II cell surface expression on macrophages IAGP N RGD:5509061 20200310 MGI PMID:16546098 1617247 Nup98 nucleoporin 98 gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20200310 MGI PMID:16546098 1617247 Nup98 nucleoporin 98 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:16546098 1617247 Nup98 nucleoporin 98 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:16546098 1617247 Nup98 nucleoporin 98 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:16546098 1617247 Nup98 nucleoporin 98 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:16546098 1617247 Nup98 nucleoporin 98 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20200310 MGI PMID:26731471 1617247 Nup98 nucleoporin 98 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11248054 1617247 Nup98 nucleoporin 98 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1617254 Cdhr2 cadherin-related family member 2 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20191031 MGI PMID:30403560 1617254 Cdhr2 cadherin-related family member 2 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20191031 MGI PMID:30403560 1617254 Cdhr2 cadherin-related family member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191031 MGI PMID:30403560 1617254 Cdhr2 cadherin-related family member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20191031 MGI PMID:30403560 1617254 Cdhr2 cadherin-related family member 2 gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20191031 MGI PMID:30403560 1617254 Cdhr2 cadherin-related family member 2 gene MP:0008109 abnormal small intestinal microvillus morphology IAGP N RGD:5509061 20191031 MGI PMID:30403560 1617254 Cdhr2 cadherin-related family member 2 gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20191031 MGI PMID:30403560 1617254 Cdhr2 cadherin-related family member 2 gene MP:0013482 abnormal duodenum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20191031 MGI PMID:30403560 1617254 Cdhr2 cadherin-related family member 2 gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20191031 MGI PMID:30403560 1617255 Plekhg3 pleckstrin homology domain containing, family G (with RhoGef domain) member 3 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20201022 MGI 1617303 Duxf4 double homeobox family member 4 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20231026 MGI PMID:31591446 1617307 Ntn5 netrin 5 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20160317 MGI PMID:26858598 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20210826 MGI 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0000745 tremors IEA N RGD:5509061 20220811 MGI 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18272690 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:18272690 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18272690 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18272690 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20220811 MGI 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:18272690 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20240523 MGI 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:18272690 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:18272690 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210826 MGI 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:18272690 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20210826 MGI 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:18272690 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:18272690 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:18272690 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20210826 MGI 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18272690 1617308 Shank1 SH3 and multiple ankyrin repeat domains 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1617310 Rgs9bp regulator of G-protein signalling 9 binding protein gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:14625292 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:21068328 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20150205 MGI PMID:24715463 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:20220021 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:21068328 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0001105 abnormal PNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21068328 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21068328 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21068328 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21068328 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:16341215 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21068328 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:16341215 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20111116 MGI 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16341215 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:21068328 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:16341215 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21068328 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21068328 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20181227 MGI 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0008155 decreased diameter of radius IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0008157 decreased diameter of ulna IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1652607 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21068328 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1617311 Lgi4 leucine-rich repeat LGI family, member 4 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1617312 Zfp14 zinc finger protein 14 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20230209 MGI PMID:36349645 1617312 Zfp14 zinc finger protein 14 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20230209 MGI PMID:36349645 1617312 Zfp14 zinc finger protein 14 gene MP:0000947 convulsive seizures IEA N RGD:5509061 20211021 MGI 1617312 Zfp14 zinc finger protein 14 gene MP:0001214 skin hyperplasia IAGP N RGD:5509061 20230209 MGI PMID:36349645 1617312 Zfp14 zinc finger protein 14 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20230209 MGI PMID:36349645 1617312 Zfp14 zinc finger protein 14 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20230209 MGI PMID:36349645 1617312 Zfp14 zinc finger protein 14 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20230209 MGI PMID:36349645 1617312 Zfp14 zinc finger protein 14 gene MP:0002083 premature death IAGP N RGD:5509061 20230209 MGI PMID:36349645 1617312 Zfp14 zinc finger protein 14 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20230209 MGI PMID:36349645 1617312 Zfp14 zinc finger protein 14 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1617312 Zfp14 zinc finger protein 14 gene MP:0003341 chronic pancreas inflammation IAGP N RGD:5509061 20230209 MGI PMID:36349645 1617312 Zfp14 zinc finger protein 14 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20230209 MGI PMID:36349645 1617313 Zfp568 zinc finger protein 568 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:18701545 1617313 Zfp568 zinc finger protein 568 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18701545 1617313 Zfp568 zinc finger protein 568 gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:23071813 1617313 Zfp568 zinc finger protein 568 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:15755804 1617313 Zfp568 zinc finger protein 568 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:21094155 1617313 Zfp568 zinc finger protein 568 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:18701545 1617313 Zfp568 zinc finger protein 568 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:18701545 1617313 Zfp568 zinc finger protein 568 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:21094155 1617313 Zfp568 zinc finger protein 568 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:21094155 1617313 Zfp568 zinc finger protein 568 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15755804 1617313 Zfp568 zinc finger protein 568 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18701545 1617313 Zfp568 zinc finger protein 568 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18701545 1617313 Zfp568 zinc finger protein 568 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:21094155 1617313 Zfp568 zinc finger protein 568 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20150416 MGI PMID:22110054 1617313 Zfp568 zinc finger protein 568 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18701545 1617313 Zfp568 zinc finger protein 568 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150416 MGI PMID:22110054 1617313 Zfp568 zinc finger protein 568 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:23071813 1617313 Zfp568 zinc finger protein 568 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:18701545 1617313 Zfp568 zinc finger protein 568 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:21094155 1617313 Zfp568 zinc finger protein 568 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:18701545 1617313 Zfp568 zinc finger protein 568 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21094155 1617313 Zfp568 zinc finger protein 568 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:21094155 1617313 Zfp568 zinc finger protein 568 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:18701545 1617313 Zfp568 zinc finger protein 568 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:18701545 1617313 Zfp568 zinc finger protein 568 gene MP:0004264 abnormal extraembryonic tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:21094155 1617313 Zfp568 zinc finger protein 568 gene MP:0004559 small allantois IAGP N RGD:5509061 20141003 MGI PMID:21094155 1617313 Zfp568 zinc finger protein 568 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:23071813 1617313 Zfp568 zinc finger protein 568 gene MP:0005655 increased aggression IAGP N RGD:5509061 20141003 MGI PMID:23071813 1617313 Zfp568 zinc finger protein 568 gene MP:0006323 abnormal extraembryonic mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:21094155 1617313 Zfp568 zinc finger protein 568 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18701545 1617313 Zfp568 zinc finger protein 568 gene MP:0008926 abnormal anterior definitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18701545 1617313 Zfp568 zinc finger protein 568 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:21094155 1617313 Zfp568 zinc finger protein 568 gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18701545 1617313 Zfp568 zinc finger protein 568 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 1617313 Zfp568 zinc finger protein 568 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:21094155 1617313 Zfp568 zinc finger protein 568 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:18701545 1617315 Azin2 antizyme inhibitor 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23874910 1617316 Dynlt4 dynein light chain Tctex-type 4 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20221110 MGI 1617316 Dynlt4 dynein light chain Tctex-type 4 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20221110 MGI 1617316 Dynlt4 dynein light chain Tctex-type 4 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20221110 MGI 1617317 Cdcp2 CUB domain containing protein 2 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1617317 Cdcp2 CUB domain containing protein 2 gene MP:0009084 blind uterus IEA N RGD:5509061 20210520 MGI 1617318 Cimap2 ciliary microtubule associated protein 2 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20151119 MGI PMID:25883318 1617318 Cimap2 ciliary microtubule associated protein 2 gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20151119 MGI PMID:25883318 1617318 Cimap2 ciliary microtubule associated protein 2 gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20151119 MGI PMID:25883318 1617318 Cimap2 ciliary microtubule associated protein 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20151119 MGI PMID:25883318 1617318 Cimap2 ciliary microtubule associated protein 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20151119 MGI PMID:25883318 1617318 Cimap2 ciliary microtubule associated protein 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20151119 MGI PMID:25883318 1617318 Cimap2 ciliary microtubule associated protein 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20151119 MGI PMID:25883318 1617318 Cimap2 ciliary microtubule associated protein 2 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20151119 MGI PMID:25883318 1617318 Cimap2 ciliary microtubule associated protein 2 gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20151119 MGI PMID:25883318 1617318 Cimap2 ciliary microtubule associated protein 2 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IAGP N RGD:5509061 20151119 MGI PMID:25883318 1617318 Cimap2 ciliary microtubule associated protein 2 gene MP:0013281 increased cytotoxic T cell cytolysis IAGP N RGD:5509061 20151119 MGI PMID:25883318 1617318 Cimap2 ciliary microtubule associated protein 2 gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:25883318 1617319 Zbtb34 zinc finger and BTB domain containing 34 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1617319 Zbtb34 zinc finger and BTB domain containing 34 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1617320 Ralgps1 Ral GEF with PH domain and SH3 binding motif 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1617320 Ralgps1 Ral GEF with PH domain and SH3 binding motif 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20231207 MGI 1617320 Ralgps1 Ral GEF with PH domain and SH3 binding motif 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1617322 H2-M5 histocompatibility 2, M region locus 5 gene MP:0002833 increased heart weight IEA N RGD:5509061 20200310 MGI 1617322 H2-M5 histocompatibility 2, M region locus 5 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200310 MGI 1617322 H2-M5 histocompatibility 2, M region locus 5 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20200310 MGI 1617323 Cchcr1 coiled-coil alpha-helical rod protein 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20211104 MGI PMID:32580135 1617323 Cchcr1 coiled-coil alpha-helical rod protein 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1617323 Cchcr1 coiled-coil alpha-helical rod protein 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210826 MGI 1617323 Cchcr1 coiled-coil alpha-helical rod protein 1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20211104 MGI PMID:32580135 1617323 Cchcr1 coiled-coil alpha-helical rod protein 1 gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20211104 MGI PMID:32580135 1617323 Cchcr1 coiled-coil alpha-helical rod protein 1 gene MP:0003848 brittle hair IAGP N RGD:5509061 20211104 MGI PMID:32580135 1617323 Cchcr1 coiled-coil alpha-helical rod protein 1 gene MP:0005387 immune system phenotype IAGP N RGD:5509061 20211104 MGI PMID:32580135 1617323 Cchcr1 coiled-coil alpha-helical rod protein 1 gene MP:0010771 integument phenotype IAGP N RGD:5509061 20211104 MGI PMID:32580135 1617324 Btnl1 butyrophilin-like 1 gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20200813 MGI PMID:27641500 1617324 Btnl1 butyrophilin-like 1 gene MP:0008401 abnormal CD8 positive, alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20200813 MGI PMID:27641500 1617325 Morc2b microrchidia 2B gene MP:0001127 small ovary IAGP N RGD:5509061 20180315 MGI PMID:29329290 1617325 Morc2b microrchidia 2B gene MP:0001147 small testis IAGP N RGD:5509061 20180315 MGI PMID:29329290 1617325 Morc2b microrchidia 2B gene MP:0001925 male infertility IAGP N RGD:5509061 20180315 MGI PMID:29329290 1617325 Morc2b microrchidia 2B gene MP:0001926 female infertility IAGP N RGD:5509061 20180315 MGI PMID:29329290 1617325 Morc2b microrchidia 2B gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20180315 MGI PMID:29329290 1617325 Morc2b microrchidia 2B gene MP:0004805 absent oocytes IAGP N RGD:5509061 20180315 MGI PMID:29329290 1617325 Morc2b microrchidia 2B gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180315 MGI PMID:29329290 1617325 Morc2b microrchidia 2B gene MP:0005159 azoospermia IAGP N RGD:5509061 20180315 MGI PMID:29329290 1617325 Morc2b microrchidia 2B gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20180315 MGI PMID:29329290 1617325 Morc2b microrchidia 2B gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20180315 MGI PMID:29329290 1617325 Morc2b microrchidia 2B gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20180315 MGI PMID:29329290 1617325 Morc2b microrchidia 2B gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20180315 MGI PMID:29329290 1617325 Morc2b microrchidia 2B gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20180315 MGI PMID:29329290 1617325 Morc2b microrchidia 2B gene MP:0031474 increased female germ cell apoptosis IAGP N RGD:5509061 20230928 MGI PMID:29329290 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15470153 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:15470153 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:12598599 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12598599 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15673435 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:19145222 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19145222 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:12598599 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12427827 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12427827 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12598599 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:19145222 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15470153 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:12427827 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:15470153 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:19145222 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0002802 abnormal discrimination learning IAGP N RGD:5509061 20141003 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12598599 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12427827 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15733080 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:12598599 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:19145222 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:19145222 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19145222 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0009848 increased horizontal stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:19145222 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15470153 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0011002 enhanced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12427827 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12598599 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15470153 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15673435 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19145222 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15733080 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0014373 increased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:15470153 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0014375 increased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:15470153 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0014384 increased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:23141534 1617329 Syngap1 synaptic Ras GTPase activating protein 1 homolog (rat) gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:19145222 1617334 Zfp760 zinc finger protein 760 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1617334 Zfp760 zinc finger protein 760 gene MP:0002492 decreased IgE level IEA N RGD:5509061 20160804 MGI 1617334 Zfp760 zinc finger protein 760 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20160804 MGI 1617334 Zfp760 zinc finger protein 760 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20160804 MGI 1617334 Zfp760 zinc finger protein 760 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20160804 MGI 1617334 Zfp760 zinc finger protein 760 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20160804 MGI 1617335 Pnldc1 poly(A)-specific ribonuclease (PARN)-like domain containing 1 gene MP:0001147 small testis IAGP N RGD:5509061 20180621 MGI PMID:29444933 1617335 Pnldc1 poly(A)-specific ribonuclease (PARN)-like domain containing 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20180621 MGI PMID:29444933 1617335 Pnldc1 poly(A)-specific ribonuclease (PARN)-like domain containing 1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20220811 MGI 1617335 Pnldc1 poly(A)-specific ribonuclease (PARN)-like domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20180621 MGI PMID:29444933 1617335 Pnldc1 poly(A)-specific ribonuclease (PARN)-like domain containing 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20180621 MGI PMID:29444933 1617335 Pnldc1 poly(A)-specific ribonuclease (PARN)-like domain containing 1 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20220811 MGI 1617336 Fam81b family with sequence similarity 81, member B gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210826 MGI 1617336 Fam81b family with sequence similarity 81, member B gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210826 MGI 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0001925 male infertility IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0009242 thin sperm flagellum IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617338 Ccdc38 coiled-coil domain containing 38 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20220630 MGI PMID:35587122 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20200310 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20200310 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20200310 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0004937 dilated heart IAGP N RGD:5509061 20200310 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20200310 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20200310 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0013289 abnormal mitotic cytokinesis IAGP N RGD:5509061 20200310 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20200310 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0031609 increased fetal cardiomyocyte size IAGP N RGD:5509061 20240321 MGI PMID:28698371 1617339 Gas2l3 growth arrest-specific 2 like 3 gene MP:0031611 decreased fetal cardiomyocyte number IAGP N RGD:5509061 20240321 MGI PMID:28698371 1617342 Lingo3 leucine rich repeat and Ig domain containing 3 gene MP:0001406 abnormal gait IEA N RGD:5509061 20230601 MGI 1617344 Il17c interleukin 17C gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:21993848 1617344 Il17c interleukin 17C gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21993848 1617344 Il17c interleukin 17C gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21982598 1617344 Il17c interleukin 17C gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21982598 1617344 Il17c interleukin 17C gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:21982598 1617344 Il17c interleukin 17C gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:21982598 1617344 Il17c interleukin 17C gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21993848 1617344 Il17c interleukin 17C gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21993848 1617347 Tmf1 TATA element modulatory factor 1 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:20691678 1617347 Tmf1 TATA element modulatory factor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20691678 1617347 Tmf1 TATA element modulatory factor 1 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:20691678 1617347 Tmf1 TATA element modulatory factor 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20691678 1617347 Tmf1 TATA element modulatory factor 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20691678 1617347 Tmf1 TATA element modulatory factor 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:20691678 1617347 Tmf1 TATA element modulatory factor 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:20691678 1617347 Tmf1 TATA element modulatory factor 1 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20141003 MGI PMID:20691678 1617347 Tmf1 TATA element modulatory factor 1 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:20691678 1617347 Tmf1 TATA element modulatory factor 1 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:20691678 1617348 Iqsec1 IQ motif and Sec7 domain 1 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:20547133 1617350 Arhgap25 Rho GTPase activating protein 25 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20170601 MGI PMID:27566826 1617350 Arhgap25 Rho GTPase activating protein 25 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170601 MGI PMID:27566826 1617350 Arhgap25 Rho GTPase activating protein 25 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20141003 MGI 1617350 Arhgap25 Rho GTPase activating protein 25 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20170601 MGI PMID:27566826 1617350 Arhgap25 Rho GTPase activating protein 25 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20170601 MGI PMID:27566826 1617350 Arhgap25 Rho GTPase activating protein 25 gene MP:0005103 abnormal retina pigmentation IEA N RGD:5509061 20141003 MGI 1617350 Arhgap25 Rho GTPase activating protein 25 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1617350 Arhgap25 Rho GTPase activating protein 25 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20170601 MGI PMID:27566826 1617350 Arhgap25 Rho GTPase activating protein 25 gene MP:0020213 enhanced leukocyte migration IAGP N RGD:5509061 20170601 MGI PMID:27566826 1617350 Arhgap25 Rho GTPase activating protein 25 gene MP:0020333 enhanced leukocyte tethering or rolling IAGP N RGD:5509061 20170601 MGI PMID:27566826 1617351 9430015G10Rik RIKEN cDNA 9430015G10 gene gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20170323 MGI 1617351 9430015G10Rik RIKEN cDNA 9430015G10 gene gene MP:0005014 increased B cell number IEA N RGD:5509061 20170323 MGI 1617351 9430015G10Rik RIKEN cDNA 9430015G10 gene gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20170323 MGI 1617353 Arhgef16 Rho guanine nucleotide exchange factor 16 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1617353 Arhgef16 Rho guanine nucleotide exchange factor 16 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1617353 Arhgef16 Rho guanine nucleotide exchange factor 16 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1617353 Arhgef16 Rho guanine nucleotide exchange factor 16 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1617353 Arhgef16 Rho guanine nucleotide exchange factor 16 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1617353 Arhgef16 Rho guanine nucleotide exchange factor 16 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1617354 Cep104 centrosomal protein 104 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1617354 Cep104 centrosomal protein 104 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 1617355 Tmem201 transmembrane protein 201 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20231123 MGI PMID:35311970 1617355 Tmem201 transmembrane protein 201 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20231123 MGI PMID:35311970 1617356 Gm572 predicted gene 572 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1617356 Gm572 predicted gene 572 gene MP:0000531 right pulmonary isomerism IEA N RGD:5509061 20141003 MGI 1617356 Gm572 predicted gene 572 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20141003 MGI 1617356 Gm572 predicted gene 572 gene MP:0000644 dextrocardia IEA N RGD:5509061 20141003 MGI 1617356 Gm572 predicted gene 572 gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20141003 MGI 1617356 Gm572 predicted gene 572 gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1617356 Gm572 predicted gene 572 gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 1617356 Gm572 predicted gene 572 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1617356 Gm572 predicted gene 572 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20201022 MGI 1617356 Gm572 predicted gene 572 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1617356 Gm572 predicted gene 572 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1617356 Gm572 predicted gene 572 gene MP:0011252 situs inversus totalis IEA N RGD:5509061 20141003 MGI 1617356 Gm572 predicted gene 572 gene MP:0011649 immotile respiratory cilia IEA N RGD:5509061 20141003 MGI 1617357 Tardbp TAR DNA binding protein gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1617357 Tardbp TAR DNA binding protein gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22718760 1617357 Tardbp TAR DNA binding protein gene MP:0000160 kyphosis IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0000745 tremors IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0000745 tremors IAGP N RGD:5509061 20220721 MGI PMID:23449777 1617357 Tardbp TAR DNA binding protein gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:22718760 1617357 Tardbp TAR DNA binding protein gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 1617357 Tardbp TAR DNA binding protein gene MP:0000798 abnormal frontal lobe morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 1617357 Tardbp TAR DNA binding protein gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22718760 1617357 Tardbp TAR DNA binding protein gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20220721 MGI PMID:23449777 1617357 Tardbp TAR DNA binding protein gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:22718760 1617357 Tardbp TAR DNA binding protein gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20200507 MGI PMID:30625319 1617357 Tardbp TAR DNA binding protein gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20220721 MGI PMID:23449777 1617357 Tardbp TAR DNA binding protein gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200402 MGI PMID:29764981 1617357 Tardbp TAR DNA binding protein gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20200507 MGI PMID:30625319 1617357 Tardbp TAR DNA binding protein gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20220721 MGI PMID:23449777 1617357 Tardbp TAR DNA binding protein gene MP:0001147 small testis IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0001260 increased body weight IAGP N RGD:5509061 20180719 MGI PMID:29556029 1617357 Tardbp TAR DNA binding protein gene MP:0001260 increased body weight IAGP N RGD:5509061 20220616 MGI PMID:34130995 1617357 Tardbp TAR DNA binding protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20660762 1617357 Tardbp TAR DNA binding protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22718760 1617357 Tardbp TAR DNA binding protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24465814 1617357 Tardbp TAR DNA binding protein gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20660762 1617357 Tardbp TAR DNA binding protein gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22718760 1617357 Tardbp TAR DNA binding protein gene MP:0001263 weight loss IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0001263 weight loss IAGP N RGD:5509061 20220721 MGI PMID:23449777 1617357 Tardbp TAR DNA binding protein gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20220616 MGI PMID:34130995 1617357 Tardbp TAR DNA binding protein gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20180719 MGI PMID:29556029 1617357 Tardbp TAR DNA binding protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22718760 1617357 Tardbp TAR DNA binding protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180719 MGI PMID:29556029 1617357 Tardbp TAR DNA binding protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20220721 MGI PMID:23449777 1617357 Tardbp TAR DNA binding protein gene MP:0001407 short stride length IAGP N RGD:5509061 20220721 MGI PMID:23449777 1617357 Tardbp TAR DNA binding protein gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20180719 MGI PMID:29556029 1617357 Tardbp TAR DNA binding protein gene MP:0001433 polyphagia IAGP N RGD:5509061 20180719 MGI PMID:29556029 1617357 Tardbp TAR DNA binding protein gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20180719 MGI PMID:29556029 1617357 Tardbp TAR DNA binding protein gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1617357 Tardbp TAR DNA binding protein gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22718760 1617357 Tardbp TAR DNA binding protein gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:24465814 1617357 Tardbp TAR DNA binding protein gene MP:0001513 limb grasping IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20180719 MGI PMID:29556029 1617357 Tardbp TAR DNA binding protein gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20170209 MGI PMID:26672899 1617357 Tardbp TAR DNA binding protein gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20220721 MGI PMID:23449777 1617357 Tardbp TAR DNA binding protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22718760 1617357 Tardbp TAR DNA binding protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24465814 1617357 Tardbp TAR DNA binding protein gene MP:0002083 premature death IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:22718760 1617357 Tardbp TAR DNA binding protein gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20220721 MGI PMID:23449777 1617357 Tardbp TAR DNA binding protein gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20180719 MGI PMID:29556029 1617357 Tardbp TAR DNA binding protein gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:20660762 1617357 Tardbp TAR DNA binding protein gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:24465814 1617357 Tardbp TAR DNA binding protein gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20180719 MGI PMID:29556029 1617357 Tardbp TAR DNA binding protein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22718760 1617357 Tardbp TAR DNA binding protein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200507 MGI PMID:30625319 1617357 Tardbp TAR DNA binding protein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20220721 MGI PMID:23449777 1617357 Tardbp TAR DNA binding protein gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0003908 decreased stereotypic behavior IAGP N RGD:5509061 20180719 MGI PMID:29556029 1617357 Tardbp TAR DNA binding protein gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20220616 MGI PMID:34130995 1617357 Tardbp TAR DNA binding protein gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20180719 MGI PMID:29556029 1617357 Tardbp TAR DNA binding protein gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:20660762 1617357 Tardbp TAR DNA binding protein gene MP:0004142 abnormal muscle tone IAGP N RGD:5509061 20141003 MGI PMID:24465814 1617357 Tardbp TAR DNA binding protein gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:22718760 1617357 Tardbp TAR DNA binding protein gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0005405 axon degeneration IAGP N RGD:5509061 20220721 MGI PMID:23449777 1617357 Tardbp TAR DNA binding protein gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:20660762 1617357 Tardbp TAR DNA binding protein gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1617357 Tardbp TAR DNA binding protein gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20170209 MGI PMID:26672899 1617357 Tardbp TAR DNA binding protein gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0008918 microgliosis IAGP N RGD:5509061 20200507 MGI PMID:30625319 1617357 Tardbp TAR DNA binding protein gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 1617357 Tardbp TAR DNA binding protein gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20660762 1617357 Tardbp TAR DNA binding protein gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20660762 1617357 Tardbp TAR DNA binding protein gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0009234 absent sperm head IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:20660762 1617357 Tardbp TAR DNA binding protein gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 1617357 Tardbp TAR DNA binding protein gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0009424 decreased extensor digitorum longus weight IAGP N RGD:5509061 20141003 MGI PMID:24465814 1617357 Tardbp TAR DNA binding protein gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20660762 1617357 Tardbp TAR DNA binding protein gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20198480 1617357 Tardbp TAR DNA binding protein gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:24465814 1617357 Tardbp TAR DNA binding protein gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200402 MGI PMID:29764981 1617357 Tardbp TAR DNA binding protein gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20220721 MGI PMID:23449777 1617357 Tardbp TAR DNA binding protein gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230601 MGI 1617357 Tardbp TAR DNA binding protein gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:20660762 1617357 Tardbp TAR DNA binding protein gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0010951 abnormal lipid oxidation IAGP N RGD:5509061 20141003 MGI PMID:20660762 1617357 Tardbp TAR DNA binding protein gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20660762 1617357 Tardbp TAR DNA binding protein gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200402 MGI PMID:29764981 1617357 Tardbp TAR DNA binding protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20014337 1617357 Tardbp TAR DNA binding protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24465814 1617357 Tardbp TAR DNA binding protein gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20198480 1617357 Tardbp TAR DNA binding protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1617357 Tardbp TAR DNA binding protein gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200402 MGI PMID:29764981 1617357 Tardbp TAR DNA binding protein gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:29556029 1617357 Tardbp TAR DNA binding protein gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0011975 neuronal cytoplasmic inclusions IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0012051 spasticity IAGP N RGD:5509061 20200430 MGI PMID:31964415 1617357 Tardbp TAR DNA binding protein gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:20014337 1617357 Tardbp TAR DNA binding protein gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20220616 MGI PMID:34130995 1617357 Tardbp TAR DNA binding protein gene MP:0012448 abnormal primary motor cortex morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 1617357 Tardbp TAR DNA binding protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230706 MGI 1617357 Tardbp TAR DNA binding protein gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220519 MGI PMID:34599968 1617357 Tardbp TAR DNA binding protein gene MP:0014114 abnormal cognition IAGP N RGD:5509061 20180719 MGI PMID:29556029 1617357 Tardbp TAR DNA binding protein gene MP:0014115 cognitive inflexibility IAGP N RGD:5509061 20180719 MGI PMID:29556029 1617357 Tardbp TAR DNA binding protein gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:24740308 1617357 Tardbp TAR DNA binding protein gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:22718760 1617357 Tardbp TAR DNA binding protein gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20220721 MGI PMID:23449777 1617361 Rsbn1 rosbin, round spermatid basic protein 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20200310 MGI 1617361 Rsbn1 rosbin, round spermatid basic protein 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20200310 MGI 1617361 Rsbn1 rosbin, round spermatid basic protein 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1617361 Rsbn1 rosbin, round spermatid basic protein 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1617361 Rsbn1 rosbin, round spermatid basic protein 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20200310 MGI 1617361 Rsbn1 rosbin, round spermatid basic protein 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1617361 Rsbn1 rosbin, round spermatid basic protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20201224 MGI PMID:28386023 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0000929 open neural tube IAGP N RGD:5509061 20201224 MGI PMID:28386023 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20201224 MGI PMID:28386023 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20201224 MGI PMID:28386023 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20201224 MGI PMID:28386023 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20201224 MGI PMID:28386023 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:9450542 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20201224 MGI PMID:28386023 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20201224 MGI PMID:28386023 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20201224 MGI PMID:28386023 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20201224 MGI PMID:9450542 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20201224 MGI PMID:28386023 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20201224 MGI PMID:28386023 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0012082 delayed heart development IAGP N RGD:5509061 20201224 MGI PMID:28386023 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20201224 MGI PMID:28386023 1617362 Csde1 cold shock domain containing E1, RNA binding gene MP:0013272 abnormal translation IAGP N RGD:5509061 20201224 MGI PMID:28386023 1617364 Otud7b OTU domain containing 7B gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23334419 1617364 Otud7b OTU domain containing 7B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23334419 1617364 Otud7b OTU domain containing 7B gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23334419 1617364 Otud7b OTU domain containing 7B gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23564640 1617364 Otud7b OTU domain containing 7B gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:23334419 1617364 Otud7b OTU domain containing 7B gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1617364 Otud7b OTU domain containing 7B gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23334419 1617364 Otud7b OTU domain containing 7B gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23334419 1617364 Otud7b OTU domain containing 7B gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1617364 Otud7b OTU domain containing 7B gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23334419 1617364 Otud7b OTU domain containing 7B gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1617364 Otud7b OTU domain containing 7B gene MP:0010675 decreased activation-induced B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23334419 1617364 Otud7b OTU domain containing 7B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1617365 BC028528 cDNA sequence BC028528 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20200611 MGI PMID:29999589 1617365 BC028528 cDNA sequence BC028528 gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20200611 MGI PMID:29999589 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20241010 MGI PMID:38270391 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0002345 abnormal lymph node primary follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20241010 MGI PMID:38270391 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20241010 MGI PMID:38270391 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20241010 MGI PMID:38270391 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0004648 decreased thoracic vertebrae number IAGP N RGD:5509061 20241010 MGI PMID:38270391 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20241010 MGI PMID:38270391 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20241010 MGI PMID:38270391 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0014474 decreased pulmonary alveolus wall thickness IAGP N RGD:5509061 20240704 MGI PMID:17276979 1617366 Slc35c1 solute carrier family 35, member C1 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20200310 MGI PMID:17276979 1617367 Pms1 PMS1 homolog 1, mismatch repair system component gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1617367 Pms1 PMS1 homolog 1, mismatch repair system component gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1617368 Nemp2 nuclear envelope integral membrane protein 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1617368 Nemp2 nuclear envelope integral membrane protein 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1617368 Nemp2 nuclear envelope integral membrane protein 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1617368 Nemp2 nuclear envelope integral membrane protein 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0003956 abnormal body size IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0008069 abnormal joint mobility IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20141003 MGI PMID:23610558 1617374 Ark2c arkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:23610558 1617378 Pcdh17 protocadherin 17 gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:23684785 1617378 Pcdh17 protocadherin 17 gene MP:0003063 increased coping response IAGP N RGD:5509061 20141003 MGI PMID:23684785 1617378 Pcdh17 protocadherin 17 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:23684785 1617378 Pcdh17 protocadherin 17 gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:23684785 1617380 Cdca7l cell division cycle associated 7 like gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1617380 Cdca7l cell division cycle associated 7 like gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1617380 Cdca7l cell division cycle associated 7 like gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1617380 Cdca7l cell division cycle associated 7 like gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1617380 Cdca7l cell division cycle associated 7 like gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1617380 Cdca7l cell division cycle associated 7 like gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1617380 Cdca7l cell division cycle associated 7 like gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1617380 Cdca7l cell division cycle associated 7 like gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1617380 Cdca7l cell division cycle associated 7 like gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1617381 Hbq1a hemoglobin, theta 1A gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1617381 Hbq1a hemoglobin, theta 1A gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1617383 Ncaph non-SMC condensin I complex, subunit H gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20160204 MGI PMID:25474630 1617383 Ncaph non-SMC condensin I complex, subunit H gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20160204 MGI PMID:25474630 1617383 Ncaph non-SMC condensin I complex, subunit H gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20160204 MGI PMID:25474630 1617383 Ncaph non-SMC condensin I complex, subunit H gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20160204 MGI PMID:25474630 1617383 Ncaph non-SMC condensin I complex, subunit H gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20160204 MGI PMID:25474630 1617383 Ncaph non-SMC condensin I complex, subunit H gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160204 MGI PMID:25474630 1617383 Ncaph non-SMC condensin I complex, subunit H gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20160204 MGI PMID:25474630 1617383 Ncaph non-SMC condensin I complex, subunit H gene MP:0012204 abnormal neuronal stem cell physiology IAGP N RGD:5509061 20160204 MGI PMID:25474630 1617384 Fcgbp Fc fragment of IgG binding protein gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 1617384 Fcgbp Fc fragment of IgG binding protein gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1617384 Fcgbp Fc fragment of IgG binding protein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1617389 Tsga10 testis specific 10 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20210805 MGI PMID:32790169 1617389 Tsga10 testis specific 10 gene MP:0001925 male infertility IAGP N RGD:5509061 20210805 MGI PMID:32790169 1617389 Tsga10 testis specific 10 gene MP:0002673 abnormal sperm number IAGP N RGD:5509061 20210805 MGI PMID:32790169 1617389 Tsga10 testis specific 10 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20210805 MGI PMID:32790169 1617389 Tsga10 testis specific 10 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20210805 MGI PMID:32790169 1617391 Kcnh8 potassium voltage-gated channel, subfamily H (eag-related), member 8 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1617391 Kcnh8 potassium voltage-gated channel, subfamily H (eag-related), member 8 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1617391 Kcnh8 potassium voltage-gated channel, subfamily H (eag-related), member 8 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1617391 Kcnh8 potassium voltage-gated channel, subfamily H (eag-related), member 8 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 1617391 Kcnh8 potassium voltage-gated channel, subfamily H (eag-related), member 8 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1617391 Kcnh8 potassium voltage-gated channel, subfamily H (eag-related), member 8 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1617391 Kcnh8 potassium voltage-gated channel, subfamily H (eag-related), member 8 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 1617391 Kcnh8 potassium voltage-gated channel, subfamily H (eag-related), member 8 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20241017 MGI PMID:37516908 1617391 Kcnh8 potassium voltage-gated channel, subfamily H (eag-related), member 8 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 1617391 Kcnh8 potassium voltage-gated channel, subfamily H (eag-related), member 8 gene MP:0005386 behavior/neurological phenotype IAGP N RGD:5509061 20241017 MGI PMID:37516908 1617391 Kcnh8 potassium voltage-gated channel, subfamily H (eag-related), member 8 gene MP:0009709 hydrometra IEA N RGD:5509061 20210826 MGI 1617392 Fer1l5 fer-1 like family member 5 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20230323 MGI PMID:36696506 1617392 Fer1l5 fer-1 like family member 5 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20230323 MGI PMID:36696506 1617392 Fer1l5 fer-1 like family member 5 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20230323 MGI PMID:36696506 1617392 Fer1l5 fer-1 like family member 5 gene MP:0031010 failure of sperm-egg fusion IAGP N RGD:5509061 20230323 MGI PMID:36696506 1617395 Irgq immunity-related GTPase family, Q gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1617395 Irgq immunity-related GTPase family, Q gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1617396 Irgc immunity related GTPase cinema gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20231207 MGI 1617396 Irgc immunity related GTPase cinema gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220721 MGI PMID:35618043 1617396 Irgc immunity related GTPase cinema gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20231207 MGI 1617396 Irgc immunity related GTPase cinema gene MP:0001488 increased startle reflex IEA N RGD:5509061 20231207 MGI 1617396 Irgc immunity related GTPase cinema gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220721 MGI PMID:35618043 1617396 Irgc immunity related GTPase cinema gene MP:0001925 male infertility IEA N RGD:5509061 20231207 MGI 1617396 Irgc immunity related GTPase cinema gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 1617396 Irgc immunity related GTPase cinema gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20240523 MGI 1617396 Irgc immunity related GTPase cinema gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1617396 Irgc immunity related GTPase cinema gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220721 MGI PMID:35618043 1617396 Irgc immunity related GTPase cinema gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220721 MGI PMID:35618043 1617396 Irgc immunity related GTPase cinema gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20220721 MGI PMID:35618043 1617396 Irgc immunity related GTPase cinema gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20220721 MGI PMID:35618043 1617397 Zfp719 zinc finger protein 719 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1617397 Zfp719 zinc finger protein 719 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20170105 MGI 1617398 Zfp175 zinc finger protein 175 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1617398 Zfp175 zinc finger protein 175 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1617400 Thsd4 thrombospondin, type I, domain containing 4 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20240418 MGI PMID:32855533 1617400 Thsd4 thrombospondin, type I, domain containing 4 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1617400 Thsd4 thrombospondin, type I, domain containing 4 gene MP:0005655 increased aggression IEA N RGD:5509061 20240523 MGI 1617400 Thsd4 thrombospondin, type I, domain containing 4 gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20240418 MGI PMID:32855533 1617400 Thsd4 thrombospondin, type I, domain containing 4 gene MP:0010470 dilated ascending aorta IAGP N RGD:5509061 20240418 MGI PMID:32855533 1617400 Thsd4 thrombospondin, type I, domain containing 4 gene MP:0010473 descending aorta dilation IAGP N RGD:5509061 20240418 MGI PMID:32855533 1617400 Thsd4 thrombospondin, type I, domain containing 4 gene MP:0010482 abnormal aortic sinus morphology IAGP N RGD:5509061 20240418 MGI PMID:32855533 1617400 Thsd4 thrombospondin, type I, domain containing 4 gene MP:0010574 dilated aorta IAGP N RGD:5509061 20240418 MGI PMID:32855533 1617400 Thsd4 thrombospondin, type I, domain containing 4 gene MP:0010575 aortic arch dilation IAGP N RGD:5509061 20240418 MGI PMID:32855533 1617401 Tbc1d16 TBC1 domain family, member 16 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20181227 MGI 1617401 Tbc1d16 TBC1 domain family, member 16 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1617401 Tbc1d16 TBC1 domain family, member 16 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20201022 MGI 1617402 Tmprss11a transmembrane protease, serine 11a gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21853097 1617402 Tmprss11a transmembrane protease, serine 11a gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1617402 Tmprss11a transmembrane protease, serine 11a gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20191031 MGI PMID:31501243 1617403 Reps2 RALBP1 associated Eps domain containing protein 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1617403 Reps2 RALBP1 associated Eps domain containing protein 2 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1617422 Dnah1 dynein, axonemal, heavy chain 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220721 MGI PMID:30734403 1617422 Dnah1 dynein, axonemal, heavy chain 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20190502 MGI 1617422 Dnah1 dynein, axonemal, heavy chain 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11371505 1617422 Dnah1 dynein, axonemal, heavy chain 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220721 MGI PMID:30734403 1617422 Dnah1 dynein, axonemal, heavy chain 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11371505 1617422 Dnah1 dynein, axonemal, heavy chain 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11371505 1617422 Dnah1 dynein, axonemal, heavy chain 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220721 MGI PMID:30734403 1617422 Dnah1 dynein, axonemal, heavy chain 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20220721 MGI PMID:30734403 1617422 Dnah1 dynein, axonemal, heavy chain 1 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220721 MGI PMID:30734403 1617422 Dnah1 dynein, axonemal, heavy chain 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20191128 MGI 1617422 Dnah1 dynein, axonemal, heavy chain 1 gene MP:0013287 abnormal acrosome reaction IAGP N RGD:5509061 20220721 MGI PMID:30734403 1617422 Dnah1 dynein, axonemal, heavy chain 1 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220721 MGI PMID:30734403 1617422 Dnah1 dynein, axonemal, heavy chain 1 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20220721 MGI PMID:30734403 1617429 Tdp1 tyrosyl-DNA phosphodiesterase 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1617429 Tdp1 tyrosyl-DNA phosphodiesterase 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17914460 1617429 Tdp1 tyrosyl-DNA phosphodiesterase 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1617429 Tdp1 tyrosyl-DNA phosphodiesterase 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1617429 Tdp1 tyrosyl-DNA phosphodiesterase 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1617429 Tdp1 tyrosyl-DNA phosphodiesterase 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:17914460 1617429 Tdp1 tyrosyl-DNA phosphodiesterase 1 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:17914460 1617429 Tdp1 tyrosyl-DNA phosphodiesterase 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1617429 Tdp1 tyrosyl-DNA phosphodiesterase 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:21390131 1617429 Tdp1 tyrosyl-DNA phosphodiesterase 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17914460 1617429 Tdp1 tyrosyl-DNA phosphodiesterase 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17948061 1617429 Tdp1 tyrosyl-DNA phosphodiesterase 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230119 MGI 1617429 Tdp1 tyrosyl-DNA phosphodiesterase 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1617429 Tdp1 tyrosyl-DNA phosphodiesterase 1 gene MP:0010947 abnormal single-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:17914460 1617430 Spata7 spermatogenesis associated 7 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20150910 MGI PMID:25398945 1617430 Spata7 spermatogenesis associated 7 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20150910 MGI PMID:25398945 1617430 Spata7 spermatogenesis associated 7 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1617430 Spata7 spermatogenesis associated 7 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20150910 MGI PMID:25398945 1617430 Spata7 spermatogenesis associated 7 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200213 MGI PMID:29100828 1617430 Spata7 spermatogenesis associated 7 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20150910 MGI PMID:25398945 1617430 Spata7 spermatogenesis associated 7 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200213 MGI PMID:29100828 1617430 Spata7 spermatogenesis associated 7 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20150910 MGI PMID:25398945 1617430 Spata7 spermatogenesis associated 7 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20150910 MGI PMID:25398945 1617430 Spata7 spermatogenesis associated 7 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200206 MGI PMID:29899041 1617430 Spata7 spermatogenesis associated 7 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200213 MGI PMID:29100828 1617430 Spata7 spermatogenesis associated 7 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20150910 MGI PMID:25398945 1617430 Spata7 spermatogenesis associated 7 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20150910 MGI PMID:25398945 1617430 Spata7 spermatogenesis associated 7 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200213 MGI PMID:29100828 1617430 Spata7 spermatogenesis associated 7 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1617430 Spata7 spermatogenesis associated 7 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1617430 Spata7 spermatogenesis associated 7 gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20200206 MGI PMID:29899041 1617431 Aspg asparaginase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1617431 Aspg asparaginase gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1617431 Aspg asparaginase gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 1617433 Mbtd1 mbt domain containing 1 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20160804 MGI 1617433 Mbtd1 mbt domain containing 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0003841 abnormal lambdoid suture morphology IAGP N RGD:5509061 20171102 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0008149 abnormal costovertebral joint morphology IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0030286 occipital bone hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:21252303 1617433 Mbtd1 mbt domain containing 1 gene MP:0030289 flat occipital bone IAGP N RGD:5509061 20171102 MGI PMID:21252303 1617434 Mgat4b mannoside acetylglucosaminyltransferase 4, isoenzyme B gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20015870 1617434 Mgat4b mannoside acetylglucosaminyltransferase 4, isoenzyme B gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20015870 1617434 Mgat4b mannoside acetylglucosaminyltransferase 4, isoenzyme B gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:20015870 1617434 Mgat4b mannoside acetylglucosaminyltransferase 4, isoenzyme B gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111215 MGI 1617434 Mgat4b mannoside acetylglucosaminyltransferase 4, isoenzyme B gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:20015870 1617434 Mgat4b mannoside acetylglucosaminyltransferase 4, isoenzyme B gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20015870 1617434 Mgat4b mannoside acetylglucosaminyltransferase 4, isoenzyme B gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:20015870 1617434 Mgat4b mannoside acetylglucosaminyltransferase 4, isoenzyme B gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:20015870 1617434 Mgat4b mannoside acetylglucosaminyltransferase 4, isoenzyme B gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:20015870 1617434 Mgat4b mannoside acetylglucosaminyltransferase 4, isoenzyme B gene MP:0010068 decreased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:20015870 1617434 Mgat4b mannoside acetylglucosaminyltransferase 4, isoenzyme B gene MP:0012222 decreased circulating prothrombin level IAGP N RGD:5509061 20141003 MGI PMID:20015870 1617434 Mgat4b mannoside acetylglucosaminyltransferase 4, isoenzyme B gene MP:0012328 decreased circulating factor VIII level IAGP N RGD:5509061 20141003 MGI PMID:20015870 1617434 Mgat4b mannoside acetylglucosaminyltransferase 4, isoenzyme B gene MP:0012359 increased partial thromboplastin time IAGP N RGD:5509061 20141003 MGI PMID:20015870 1617434 Mgat4b mannoside acetylglucosaminyltransferase 4, isoenzyme B gene MP:0012615 decreased circulating factor IX level IAGP N RGD:5509061 20141003 MGI PMID:20015870 1617434 Mgat4b mannoside acetylglucosaminyltransferase 4, isoenzyme B gene MP:0031164 decreased circulating von Willebrand factor level IAGP N RGD:5509061 20201015 MGI PMID:20015870 1617435 Gpat4 glycerol-3-phosphate acyltransferase 4 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20200310 MGI PMID:16449762 1617435 Gpat4 glycerol-3-phosphate acyltransferase 4 gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20200310 MGI PMID:16449762 1617435 Gpat4 glycerol-3-phosphate acyltransferase 4 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20200310 MGI PMID:16449762 1617435 Gpat4 glycerol-3-phosphate acyltransferase 4 gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:16449762 1617435 Gpat4 glycerol-3-phosphate acyltransferase 4 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20200310 MGI PMID:16449762 1617435 Gpat4 glycerol-3-phosphate acyltransferase 4 gene MP:0010769 abnormal survival IEA N RGD:5509061 20200310 MGI 1617435 Gpat4 glycerol-3-phosphate acyltransferase 4 gene MP:0013716 hypolactation IAGP N RGD:5509061 20200310 MGI PMID:16449762 1617436 Nfxl1 nuclear transcription factor, X-box binding-like 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20141003 MGI 1617436 Nfxl1 nuclear transcription factor, X-box binding-like 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1617436 Nfxl1 nuclear transcription factor, X-box binding-like 1 gene MP:0002764 short tibia IEA N RGD:5509061 20141003 MGI 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20200310 MGI PMID:20215345 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20200310 MGI PMID:20215345 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:20215345 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20200310 MGI PMID:20215345 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0000914 exencephaly IEA N RGD:5509061 20230119 MGI 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:19966784 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0001697 abnormal embryo size IAGP N RGD:5509061 20200310 MGI PMID:19966784 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20200310 MGI PMID:20215345 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20230119 MGI 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:23968836 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0003052 omphalocele IAGP N RGD:5509061 20200310 MGI PMID:19966784 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0003054 spina bifida IAGP N RGD:5509061 20200310 MGI PMID:19966784 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0003641 small lung IAGP N RGD:5509061 20200310 MGI PMID:21559415 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20200310 MGI PMID:20215345 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20200310 MGI PMID:20215345 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20200310 MGI PMID:20215345 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20200310 MGI PMID:20215345 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20200310 MGI PMID:20215345 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20200310 MGI PMID:19966784 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20200310 MGI PMID:20215345 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20200310 MGI PMID:19966784 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20200310 MGI PMID:20215345 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20200310 MGI PMID:19966784 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20200310 MGI PMID:20215345 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20200310 MGI PMID:21559415 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20200310 MGI PMID:19966784 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20200310 MGI PMID:21559415 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19966784 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19966784 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20215345 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19966784 1617437 Sec24b SEC24 homolog B, COPII coat complex component gene MP:0011495 abnormal head shape IEA N RGD:5509061 20230119 MGI 1617438 Tchh trichohyalin gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1617439 Smap1 small ArfGAP 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20220922 MGI PMID:26296315 1617439 Smap1 small ArfGAP 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20150402 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20220922 MGI PMID:26296315 1617439 Smap1 small ArfGAP 1 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0010178 increased number of Howell-Jolly bodies IAGP N RGD:5509061 20141003 MGI PMID:23434593 1617439 Smap1 small ArfGAP 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20220922 MGI PMID:26296315 1617439 Smap1 small ArfGAP 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20220922 MGI PMID:26296315 1617439 Smap1 small ArfGAP 1 gene MP:0030951 abnormal endocytosis IAGP N RGD:5509061 20220922 MGI PMID:23434593 1617440 D630023F18Rik RIKEN cDNA D630023F18 gene gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1617440 D630023F18Rik RIKEN cDNA D630023F18 gene gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200310 MGI PMID:23918388 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20200310 MGI PMID:17636028 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20200310 MGI PMID:18172001 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20200310 MGI PMID:17636028 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0000524 decreased renal tubule number IAGP N RGD:5509061 20200310 MGI PMID:23555292 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20200310 MGI PMID:23555292 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:23555292 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20200310 MGI PMID:26109051 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20200310 MGI PMID:19498055 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20200310 MGI PMID:17636028 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20200310 MGI PMID:18172001 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001255 decreased body height IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:17636028 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:17636028 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20200310 MGI PMID:18172001 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20200310 MGI PMID:23918388 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20200310 MGI PMID:17636028 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:17636028 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:19498055 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001923 reduced female fertility IEA N RGD:5509061 20200310 MGI 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20200310 MGI PMID:17636028 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20200310 MGI PMID:18172001 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20200310 MGI PMID:19498055 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:23918388 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20200310 MGI PMID:19498055 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200310 MGI PMID:23918388 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0002704 tubular nephritis IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:23918388 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20200310 MGI PMID:18172001 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20200310 MGI PMID:17636028 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20200310 MGI PMID:18172001 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20200310 MGI PMID:18172001 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:23918388 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0003606 kidney failure IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:20412773 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20200310 MGI PMID:23555292 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:19498055 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20200310 MGI PMID:23555292 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0004882 enlarged lung IAGP N RGD:5509061 20200310 MGI PMID:19498055 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0004969 pale kidney IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0004969 pale kidney IAGP N RGD:5509061 20200310 MGI PMID:18172001 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20200310 MGI PMID:19498055 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20200310 MGI PMID:19498055 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20200310 MGI PMID:19498055 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20200310 MGI PMID:17636028 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20200310 MGI PMID:18172001 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20200310 MGI PMID:23918388 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0009051 dilated distal convoluted tubule IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20200310 MGI PMID:17636028 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0010500 myocardium hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:23918388 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0010887 pale lung IAGP N RGD:5509061 20200310 MGI PMID:19498055 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0010903 abnormal pulmonary alveolus wall morphology IAGP N RGD:5509061 20200310 MGI PMID:17636028 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0010922 alveolitis IAGP N RGD:5509061 20200310 MGI PMID:19498055 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0011045 decreased lung elastance IAGP N RGD:5509061 20200310 MGI PMID:19498055 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23918388 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18172001 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23918388 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18172001 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19289085 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17636028 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0011308 kidney corticomedullary cyst IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20200310 MGI PMID:17251353 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0012236 abnormal cholangiocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0013611 abnormal bile duct epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:26109051 1617441 Wwtr1 WW domain containing transcription regulator 1 gene MP:0014474 decreased pulmonary alveolus wall thickness IAGP N RGD:5509061 20240704 MGI PMID:19498055 1617445 Ftx Ftx transcript, Xist regulator, non-protein coding gene MP:0001297 microphthalmia IAGP N RGD:5509061 20190502 MGI PMID:30237402 1617445 Ftx Ftx transcript, Xist regulator, non-protein coding gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20190502 MGI PMID:30237402 1617445 Ftx Ftx transcript, Xist regulator, non-protein coding gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180628 MGI PMID:24899465 1617445 Ftx Ftx transcript, Xist regulator, non-protein coding gene MP:0003078 aphakia IAGP N RGD:5509061 20190502 MGI PMID:30237402 1617445 Ftx Ftx transcript, Xist regulator, non-protein coding gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20190502 MGI PMID:30237402 1617445 Ftx Ftx transcript, Xist regulator, non-protein coding gene MP:0010382 abnormal dosage compensation, by inactivation of X chromosome IAGP N RGD:5509061 20190502 MGI PMID:30237402 1617449 Ak7 adenylate kinase 7 gene MP:0000160 kyphosis IEA N RGD:5509061 20230119 MGI 1617449 Ak7 adenylate kinase 7 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1617449 Ak7 adenylate kinase 7 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1617449 Ak7 adenylate kinase 7 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1617449 Ak7 adenylate kinase 7 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1617449 Ak7 adenylate kinase 7 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1617449 Ak7 adenylate kinase 7 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:18776131 1617449 Ak7 adenylate kinase 7 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20230119 MGI 1617449 Ak7 adenylate kinase 7 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1617449 Ak7 adenylate kinase 7 gene MP:0001147 small testis IEA N RGD:5509061 20230119 MGI 1617449 Ak7 adenylate kinase 7 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21746835 1617449 Ak7 adenylate kinase 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18776131 1617449 Ak7 adenylate kinase 7 gene MP:0001867 rhinitis IAGP N RGD:5509061 20141003 MGI PMID:18776131 1617449 Ak7 adenylate kinase 7 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:18776131 1617449 Ak7 adenylate kinase 7 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21746835 1617449 Ak7 adenylate kinase 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18776131 1617449 Ak7 adenylate kinase 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21746835 1617449 Ak7 adenylate kinase 7 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1617449 Ak7 adenylate kinase 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18776131 1617449 Ak7 adenylate kinase 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21746835 1617449 Ak7 adenylate kinase 7 gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:18776131 1617449 Ak7 adenylate kinase 7 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21746835 1617449 Ak7 adenylate kinase 7 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20231207 MGI 1617449 Ak7 adenylate kinase 7 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:18776131 1617449 Ak7 adenylate kinase 7 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20230119 MGI 1617449 Ak7 adenylate kinase 7 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:18776131 1617449 Ak7 adenylate kinase 7 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:18776131 1617449 Ak7 adenylate kinase 7 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:18776131 1617449 Ak7 adenylate kinase 7 gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20141003 MGI PMID:21746835 1617449 Ak7 adenylate kinase 7 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:18776131 1617449 Ak7 adenylate kinase 7 gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:18776131 1617449 Ak7 adenylate kinase 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1617449 Ak7 adenylate kinase 7 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20141003 MGI PMID:21746835 1617449 Ak7 adenylate kinase 7 gene MP:0030118 rhinosinusitis IAGP N RGD:5509061 20210211 MGI PMID:21746835 1617450 Nup210l nucleoporin 210-like gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:20034429 1617450 Nup210l nucleoporin 210-like gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:20034429 1617450 Nup210l nucleoporin 210-like gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:20034429 1617450 Nup210l nucleoporin 210-like gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200310 MGI PMID:20034429 1617450 Nup210l nucleoporin 210-like gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:20034429 1617450 Nup210l nucleoporin 210-like gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20200310 MGI PMID:20034429 1617450 Nup210l nucleoporin 210-like gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20200310 MGI PMID:20034429 1617450 Nup210l nucleoporin 210-like gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20200310 MGI PMID:20034429 1617452 Ddx10 DEAD box helicase 10 gene MP:0000111 cleft palate IAGP N RGD:5509061 20151112 MGI PMID:26234751 1617452 Ddx10 DEAD box helicase 10 gene MP:0000445 short snout IAGP N RGD:5509061 20151112 MGI PMID:26234751 1617452 Ddx10 DEAD box helicase 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151112 MGI PMID:26234751 1617452 Ddx10 DEAD box helicase 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151112 MGI PMID:26234751 1617452 Ddx10 DEAD box helicase 10 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 1617452 Ddx10 DEAD box helicase 10 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241010 MGI 1617452 Ddx10 DEAD box helicase 10 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20151112 MGI PMID:26234751 1617452 Ddx10 DEAD box helicase 10 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1617452 Ddx10 DEAD box helicase 10 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20151112 MGI PMID:26234751 1617452 Ddx10 DEAD box helicase 10 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241010 MGI 1617452 Ddx10 DEAD box helicase 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1617452 Ddx10 DEAD box helicase 10 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20151112 MGI PMID:26234751 1617452 Ddx10 DEAD box helicase 10 gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20241010 MGI 1617452 Ddx10 DEAD box helicase 10 gene MP:0013618 decreased areal bone mineral density IAGP N RGD:5509061 20151112 MGI PMID:26234751 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0000160 kyphosis IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20151126 MGI PMID:24613482 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20151126 MGI PMID:24613482 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20151126 MGI PMID:24613482 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0000745 tremors IEA N RGD:5509061 20201231 MGI 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0000747 muscle weakness IAGP N RGD:5509061 20151126 MGI PMID:24613482 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0001304 cataract IEA N RGD:5509061 20160421 MGI 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20151126 MGI PMID:24613482 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0002083 premature death IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0002083 premature death IAGP N RGD:5509061 20151126 MGI PMID:24613482 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20151126 MGI PMID:24613482 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20151126 MGI PMID:24613482 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20151126 MGI PMID:24613482 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210826 MGI 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20151126 MGI PMID:24613482 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20210128 MGI 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0005440 increased glycogen level IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20151126 MGI PMID:24613482 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20151126 MGI PMID:24613482 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20151126 MGI PMID:24613482 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20151126 MGI PMID:24613482 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20150924 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20160310 MGI PMID:24613482 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20160310 MGI PMID:25092169 1617454 Agl amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene MP:0014074 increased brain glycogen level IAGP N RGD:5509061 20160310 MGI PMID:25092169 1617455 Shisa4 shisa family member 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1617455 Shisa4 shisa family member 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:17481602 1617455 Shisa4 shisa family member 4 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1617455 Shisa4 shisa family member 4 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1617460 Zfp266 zinc finger protein 266 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1617460 Zfp266 zinc finger protein 266 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1617461 Tsen54 tRNA splicing endonuclease subunit 54 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240926 MGI 1617461 Tsen54 tRNA splicing endonuclease subunit 54 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1617461 Tsen54 tRNA splicing endonuclease subunit 54 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200416 MGI PMID:29170794 1617461 Tsen54 tRNA splicing endonuclease subunit 54 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1617461 Tsen54 tRNA splicing endonuclease subunit 54 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1617461 Tsen54 tRNA splicing endonuclease subunit 54 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240926 MGI 1617462 0610040J01Rik RIKEN cDNA 0610040J01 gene gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1617462 0610040J01Rik RIKEN cDNA 0610040J01 gene gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1617462 0610040J01Rik RIKEN cDNA 0610040J01 gene gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1617462 0610040J01Rik RIKEN cDNA 0610040J01 gene gene MP:0000692 small spleen IEA N RGD:5509061 20230601 MGI 1617462 0610040J01Rik RIKEN cDNA 0610040J01 gene gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1617468 Jakmip2 janus kinase and microtubule interacting protein 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20230601 MGI 1617468 Jakmip2 janus kinase and microtubule interacting protein 2 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20220519 MGI 1617468 Jakmip2 janus kinase and microtubule interacting protein 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1617468 Jakmip2 janus kinase and microtubule interacting protein 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1617468 Jakmip2 janus kinase and microtubule interacting protein 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220519 MGI 1617468 Jakmip2 janus kinase and microtubule interacting protein 2 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1617468 Jakmip2 janus kinase and microtubule interacting protein 2 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1617468 Jakmip2 janus kinase and microtubule interacting protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1617469 Rab11fip2 RAB11 family interacting protein 2 (class I) gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1617469 Rab11fip2 RAB11 family interacting protein 2 (class I) gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1617469 Rab11fip2 RAB11 family interacting protein 2 (class I) gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 1617469 Rab11fip2 RAB11 family interacting protein 2 (class I) gene MP:0001297 microphthalmia IEA N RGD:5509061 20230119 MGI 1617469 Rab11fip2 RAB11 family interacting protein 2 (class I) gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1617469 Rab11fip2 RAB11 family interacting protein 2 (class I) gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230119 MGI 1617478 Slc35f6 solute carrier family 35, member F6 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1617478 Slc35f6 solute carrier family 35, member F6 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:19332562 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21896782 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:19332562 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:21896782 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:19332562 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:21896782 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:19332562 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:21896782 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21896782 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:19332562 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:21896782 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:19332562 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0003718 maternal effect IAGP N RGD:5509061 20220120 MGI PMID:34931676 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:19332562 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:19332562 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:19332562 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:19332562 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21896782 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21896782 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:21896782 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19332562 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21896782 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19332562 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21896782 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21896782 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21896782 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21896782 1617480 Dppa4 developmental pluripotency associated 4 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20220120 MGI PMID:34931676 1617481 Atg16l2 autophagy related 16 like 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20200310 MGI 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18802469 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21103378 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20180201 MGI PMID:28254886 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20180201 MGI PMID:28254886 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18802469 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:18802469 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:18802469 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001925 male infertility IAGP N RGD:5509061 20180201 MGI PMID:28254886 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18802469 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20180201 MGI PMID:28254886 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18802469 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18802469 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:18802469 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20180201 MGI PMID:28254886 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18802469 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180201 MGI PMID:28254886 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:18802469 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20180201 MGI PMID:28254886 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18802469 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21103378 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20180201 MGI PMID:28254886 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20141003 MGI PMID:21103378 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20180201 MGI PMID:28254886 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18802469 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21103378 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0013248 placenta junctional zone necrosis IAGP N RGD:5509061 20141003 MGI PMID:23674551 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20180201 MGI PMID:28254886 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:18802469 1617482 Tex19.1 testis expressed gene 19.1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:23674551 1617483 Psma8 proteasome subunit alpha 8 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20220519 MGI 1617483 Psma8 proteasome subunit alpha 8 gene MP:0000706 small thymus IEA N RGD:5509061 20220519 MGI 1617483 Psma8 proteasome subunit alpha 8 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:31358751 1617483 Psma8 proteasome subunit alpha 8 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:31358751 1617483 Psma8 proteasome subunit alpha 8 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:31358751 1617483 Psma8 proteasome subunit alpha 8 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20220519 MGI 1617483 Psma8 proteasome subunit alpha 8 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1617483 Psma8 proteasome subunit alpha 8 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1617483 Psma8 proteasome subunit alpha 8 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20220519 MGI 1617483 Psma8 proteasome subunit alpha 8 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20200310 MGI PMID:31358751 1617483 Psma8 proteasome subunit alpha 8 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:31358751 1617483 Psma8 proteasome subunit alpha 8 gene MP:0004930 small epididymis IEA N RGD:5509061 20220519 MGI 1617483 Psma8 proteasome subunit alpha 8 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:31358751 1617483 Psma8 proteasome subunit alpha 8 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:31358751 1617483 Psma8 proteasome subunit alpha 8 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20200310 MGI PMID:31358751 1617483 Psma8 proteasome subunit alpha 8 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20200310 MGI PMID:31358751 1617483 Psma8 proteasome subunit alpha 8 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1617494 Brap BRCA1 associated protein gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1617494 Brap BRCA1 associated protein gene MP:0000923 abnormal roof plate morphology IAGP N RGD:5509061 20141003 MGI PMID:23673330 1617494 Brap BRCA1 associated protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23673330 1617494 Brap BRCA1 associated protein gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1617494 Brap BRCA1 associated protein gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1617494 Brap BRCA1 associated protein gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20201022 MGI 1617494 Brap BRCA1 associated protein gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1617494 Brap BRCA1 associated protein gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20201022 MGI 1617494 Brap BRCA1 associated protein gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1617494 Brap BRCA1 associated protein gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:23673330 1617494 Brap BRCA1 associated protein gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:23673330 1617494 Brap BRCA1 associated protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1617494 Brap BRCA1 associated protein gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1617494 Brap BRCA1 associated protein gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1617495 2610035D17Rik RIKEN cDNA 2610035D17 gene gene MP:0012416 decreased gland tumor incidence IAGP N RGD:5509061 20231102 MGI PMID:36241718 1617496 2210408I21Rik RIKEN cDNA 2210408I21 gene gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1617496 2210408I21Rik RIKEN cDNA 2210408I21 gene gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1617496 2210408I21Rik RIKEN cDNA 2210408I21 gene gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1617496 2210408I21Rik RIKEN cDNA 2210408I21 gene gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 1617496 2210408I21Rik RIKEN cDNA 2210408I21 gene gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1617496 2210408I21Rik RIKEN cDNA 2210408I21 gene gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1617496 2210408I21Rik RIKEN cDNA 2210408I21 gene gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20181227 MGI 1617496 2210408I21Rik RIKEN cDNA 2210408I21 gene gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1617497 Borcs8 BLOC-1 related complex subunit 8 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1617499 Amer1 APC membrane recruitment 1 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0004199 increased fetal size IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0009432 increased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0020138 delayed bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0030316 enlarged neurocranium IAGP N RGD:5509061 20171109 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0030388 large fontanelles IAGP N RGD:5509061 20171214 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0030393 delayed fontanelle closure IAGP N RGD:5509061 20171214 MGI PMID:21571217 1617499 Amer1 APC membrane recruitment 1 gene MP:0030885 increased radius size IAGP N RGD:5509061 20181101 MGI PMID:21571217 1617501 Kifbp kinesin family binding protein gene MP:0000111 cleft palate IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20180517 MGI PMID:29192291 1617501 Kifbp kinesin family binding protein gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0001093 small trigeminal ganglion IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180517 MGI PMID:29192291 1617501 Kifbp kinesin family binding protein gene MP:0001575 cyanosis IAGP N RGD:5509061 20180517 MGI PMID:29192291 1617501 Kifbp kinesin family binding protein gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20180517 MGI PMID:29192291 1617501 Kifbp kinesin family binding protein gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1617501 Kifbp kinesin family binding protein gene MP:0001954 respiratory distress IAGP N RGD:5509061 20180517 MGI PMID:29192291 1617501 Kifbp kinesin family binding protein gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20180517 MGI PMID:29192291 1617501 Kifbp kinesin family binding protein gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 1617501 Kifbp kinesin family binding protein gene MP:0003595 epididymal cyst IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0004163 abnormal adenohypophysis morphology IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20180517 MGI PMID:29192291 1617501 Kifbp kinesin family binding protein gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1617501 Kifbp kinesin family binding protein gene MP:0009946 abnormal olfactory bulb layer morphology IAGP N RGD:5509061 20180517 MGI PMID:29192291 1617501 Kifbp kinesin family binding protein gene MP:0010059 olfactory bulb hypoplasia IAGP N RGD:5509061 20180517 MGI PMID:29192291 1617501 Kifbp kinesin family binding protein gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180517 MGI PMID:29192291 1617501 Kifbp kinesin family binding protein gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1617501 Kifbp kinesin family binding protein gene MP:0013001 abnormal enteric neural crest cell morphology IAGP N RGD:5509061 20180517 MGI PMID:29192291 1617501 Kifbp kinesin family binding protein gene MP:0013247 placenta necrosis IAGP N RGD:5509061 20190912 MGI PMID:29539633 1617501 Kifbp kinesin family binding protein gene MP:0013832 thin vagus nerve IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0013873 abnormal ductus venosus morphology IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0013874 abnormal ductus venosus topology IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0013875 increased trigeminal neuroma incidence IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0014002 absent extracranial vertebral artery segment IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0014006 absent posterior communicating artery IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0014018 embryo tumor IEA N RGD:5509061 20170504 MGI 1617501 Kifbp kinesin family binding protein gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:29539633 1617503 2510002D24Rik RIKEN cDNA 2510002D24 gene gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210520 MGI 1617503 2510002D24Rik RIKEN cDNA 2510002D24 gene gene MP:0001147 small testis IEA N RGD:5509061 20210520 MGI 1617503 2510002D24Rik RIKEN cDNA 2510002D24 gene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190221 MGI PMID:29571919 1617503 2510002D24Rik RIKEN cDNA 2510002D24 gene gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210520 MGI 1617503 2510002D24Rik RIKEN cDNA 2510002D24 gene gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210520 MGI 1617505 Shisal1 shisa like 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20200514 MGI 1617505 Shisal1 shisa like 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20200514 MGI 1617505 Shisal1 shisa like 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20200514 MGI 1617505 Shisal1 shisa like 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200514 MGI 1617505 Shisal1 shisa like 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1617505 Shisal1 shisa like 1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20240523 MGI 1617505 Shisal1 shisa like 1 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20200514 MGI 1617505 Shisal1 shisa like 1 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20200514 MGI 1617505 Shisal1 shisa like 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20200514 MGI 1617505 Shisal1 shisa like 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220519 MGI 1617505 Shisal1 shisa like 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1617509 Arhgap19 Rho GTPase activating protein 19 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1617509 Arhgap19 Rho GTPase activating protein 19 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1617509 Arhgap19 Rho GTPase activating protein 19 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22045912 1617509 Arhgap19 Rho GTPase activating protein 19 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1617511 Stox2 storkhead box 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1617511 Stox2 storkhead box 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20201022 MGI 1617511 Stox2 storkhead box 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 1617511 Stox2 storkhead box 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1617511 Stox2 storkhead box 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1617516 Prss55 serine protease 55 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 1617516 Prss55 serine protease 55 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 1617516 Prss55 serine protease 55 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1617516 Prss55 serine protease 55 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1617516 Prss55 serine protease 55 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1617516 Prss55 serine protease 55 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1617516 Prss55 serine protease 55 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1617516 Prss55 serine protease 55 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 1617516 Prss55 serine protease 55 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230119 MGI 1617516 Prss55 serine protease 55 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200924 MGI PMID:32301961 1617516 Prss55 serine protease 55 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220721 MGI PMID:33417308 1617516 Prss55 serine protease 55 gene MP:0001925 male infertility IAGP N RGD:5509061 20190912 MGI PMID:30032357 1617516 Prss55 serine protease 55 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230119 MGI 1617516 Prss55 serine protease 55 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1617516 Prss55 serine protease 55 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220721 MGI PMID:33417308 1617516 Prss55 serine protease 55 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20230119 MGI 1617516 Prss55 serine protease 55 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20220721 MGI PMID:33417308 1617516 Prss55 serine protease 55 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20230119 MGI 1617516 Prss55 serine protease 55 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220721 MGI PMID:33417308 1617516 Prss55 serine protease 55 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220721 MGI PMID:33417308 1617516 Prss55 serine protease 55 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220721 MGI PMID:33417308 1617516 Prss55 serine protease 55 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220721 MGI PMID:33417308 1617516 Prss55 serine protease 55 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20190912 MGI PMID:30032357 1617516 Prss55 serine protease 55 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20200924 MGI PMID:32301961 1617516 Prss55 serine protease 55 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220721 MGI PMID:33417308 1617516 Prss55 serine protease 55 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220721 MGI PMID:33417308 1617516 Prss55 serine protease 55 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20220721 MGI PMID:33417308 1617516 Prss55 serine protease 55 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20220721 MGI PMID:33417308 1617516 Prss55 serine protease 55 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220721 MGI PMID:33417308 1617516 Prss55 serine protease 55 gene MP:0030977 impaired sperm-egg recognition IAGP N RGD:5509061 20191226 MGI PMID:30032357 1617516 Prss55 serine protease 55 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:30032357 1617516 Prss55 serine protease 55 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220303 MGI PMID:30032357 1617516 Prss55 serine protease 55 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220721 MGI PMID:33417308 1617522 1500009L16Rik RIKEN cDNA 1500009L16 gene gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1617522 1500009L16Rik RIKEN cDNA 1500009L16 gene gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210520 MGI 1617522 1500009L16Rik RIKEN cDNA 1500009L16 gene gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1617522 1500009L16Rik RIKEN cDNA 1500009L16 gene gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1617522 1500009L16Rik RIKEN cDNA 1500009L16 gene gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20240523 MGI 1617527 Iqcn IQ motif containing N gene MP:0001925 male infertility IAGP N RGD:5509061 20230112 MGI PMID:36321563 1617527 Iqcn IQ motif containing N gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20230112 MGI PMID:36321563 1617527 Iqcn IQ motif containing N gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20230112 MGI PMID:36321563 1617527 Iqcn IQ motif containing N gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20230112 MGI PMID:36321563 1617527 Iqcn IQ motif containing N gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20230112 MGI PMID:36321563 1617527 Iqcn IQ motif containing N gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20230112 MGI PMID:36321563 1617527 Iqcn IQ motif containing N gene MP:0031386 elongated manchette IAGP N RGD:5509061 20230112 MGI PMID:36321563 1617531 Smyd3 SET and MYND domain containing 3 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20220721 MGI PMID:32779886 1617531 Smyd3 SET and MYND domain containing 3 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20220721 MGI PMID:32779886 1617531 Smyd3 SET and MYND domain containing 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160915 MGI PMID:24652767 1617531 Smyd3 SET and MYND domain containing 3 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20220721 MGI PMID:32779886 1617531 Smyd3 SET and MYND domain containing 3 gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20220721 MGI PMID:32779886 1617534 Arap1 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 1617534 Arap1 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20231207 MGI 1617534 Arap1 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1 gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 1617534 Arap1 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 1617534 Arap1 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1617534 Arap1 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1 gene MP:0005574 decreased pulmonary respiratory rate IEA N RGD:5509061 20201022 MGI 1617534 Arap1 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1 gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 1617540 Mob1b MOB kinase activator 1B gene MP:0000120 malocclusion IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0000420 ruffled hair IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0000599 enlarged liver IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617540 Mob1b MOB kinase activator 1B gene MP:0000611 jaundice IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617540 Mob1b MOB kinase activator 1B gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0001525 impaired balance IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617540 Mob1b MOB kinase activator 1B gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617540 Mob1b MOB kinase activator 1B gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0003158 dysphagia IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0003252 abnormal bile duct physiology IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617540 Mob1b MOB kinase activator 1B gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617540 Mob1b MOB kinase activator 1B gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617540 Mob1b MOB kinase activator 1B gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617540 Mob1b MOB kinase activator 1B gene MP:0003427 parakeratosis IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0003769 abnormal lip morphology IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617540 Mob1b MOB kinase activator 1B gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617540 Mob1b MOB kinase activator 1B gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0009581 decreased keratinocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0009877 exostosis IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0010293 increased integument system tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0010297 increased hepatobiliary system tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617540 Mob1b MOB kinase activator 1B gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617540 Mob1b MOB kinase activator 1B gene MP:0010318 increased salivary gland tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617540 Mob1b MOB kinase activator 1B gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0011686 increased epidermal stem cell number IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20200310 MGI PMID:23143302 1617540 Mob1b MOB kinase activator 1B gene MP:0012236 abnormal cholangiocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617540 Mob1b MOB kinase activator 1B gene MP:0013119 abdomen swellings IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617540 Mob1b MOB kinase activator 1B gene MP:0014038 increased hepatocyte number IAGP N RGD:5509061 20200310 MGI PMID:26699479 1617544 Nrn1 neuritin 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22190461 1617544 Nrn1 neuritin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22190461 1617544 Nrn1 neuritin 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:22190461 1617544 Nrn1 neuritin 1 gene MP:0002924 delayed CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:22190461 1617544 Nrn1 neuritin 1 gene MP:0002946 delayed axon extension IAGP N RGD:5509061 20141003 MGI PMID:22190461 1617544 Nrn1 neuritin 1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:22190461 1617544 Nrn1 neuritin 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22190461 1617544 Nrn1 neuritin 1 gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:22190461 1617544 Nrn1 neuritin 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22190461 1617544 Nrn1 neuritin 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22190461 1617544 Nrn1 neuritin 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22190461 1617544 Nrn1 neuritin 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:22190461 1617544 Nrn1 neuritin 1 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20180301 MGI PMID:22190461 1617547 Zmat5 zinc finger, matrin type 5 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 1617547 Zmat5 zinc finger, matrin type 5 gene MP:0005544 cornea deposits IEA N RGD:5509061 20230601 MGI 1617547 Zmat5 zinc finger, matrin type 5 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1617547 Zmat5 zinc finger, matrin type 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1617548 Dram2 DNA-damage regulated autophagy modulator 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20181227 MGI 1617548 Dram2 DNA-damage regulated autophagy modulator 2 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20231221 MGI PMID:37691820 1617548 Dram2 DNA-damage regulated autophagy modulator 2 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20231221 MGI PMID:37691820 1617548 Dram2 DNA-damage regulated autophagy modulator 2 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20231221 MGI PMID:37691820 1617548 Dram2 DNA-damage regulated autophagy modulator 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20231221 MGI PMID:37691820 1617548 Dram2 DNA-damage regulated autophagy modulator 2 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20231221 MGI PMID:37691820 1617549 Lpar6 lysophosphatidic acid receptor 6 gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20240801 MGI PMID:38676926 1617549 Lpar6 lysophosphatidic acid receptor 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1617549 Lpar6 lysophosphatidic acid receptor 6 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1617549 Lpar6 lysophosphatidic acid receptor 6 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20240801 MGI PMID:38676926 1617549 Lpar6 lysophosphatidic acid receptor 6 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1617549 Lpar6 lysophosphatidic acid receptor 6 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:28486600 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0000562 polydactyly IEA N RGD:5509061 20221215 MGI 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20200402 MGI 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20180201 MGI PMID:16015333 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20180201 MGI PMID:16015333 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:16015333 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20180201 MGI PMID:16015333 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:16015333 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:28486600 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20180201 MGI PMID:28486600 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20180201 MGI PMID:28486600 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20180201 MGI PMID:16015333 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20180201 MGI PMID:28486600 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20180201 MGI PMID:28486600 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20180201 MGI PMID:28486600 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180201 MGI PMID:28486600 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20180201 MGI PMID:28486600 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20180201 MGI PMID:28486600 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20180201 MGI PMID:28486600 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20180201 MGI PMID:16015333 1617550 Sclt1 sodium channel and clathrin linker 1 gene MP:0013916 decreased intestine length IAGP N RGD:5509061 20180201 MGI PMID:28486600 1617552 Cfap418 cilia and flagella associated protein 418 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20180607 MGI PMID:29440555 1617552 Cfap418 cilia and flagella associated protein 418 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20180607 MGI PMID:29440555 1617552 Cfap418 cilia and flagella associated protein 418 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20180607 MGI PMID:29440555 1617552 Cfap418 cilia and flagella associated protein 418 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1617552 Cfap418 cilia and flagella associated protein 418 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20180607 MGI PMID:29440555 1617552 Cfap418 cilia and flagella associated protein 418 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20180607 MGI PMID:29440555 1617552 Cfap418 cilia and flagella associated protein 418 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20180607 MGI PMID:29440555 1617552 Cfap418 cilia and flagella associated protein 418 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20180607 MGI PMID:29440555 1617552 Cfap418 cilia and flagella associated protein 418 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20180607 MGI PMID:29440555 1617552 Cfap418 cilia and flagella associated protein 418 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20180607 MGI PMID:29440555 1617552 Cfap418 cilia and flagella associated protein 418 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20180607 MGI PMID:29440555 1617552 Cfap418 cilia and flagella associated protein 418 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20180607 MGI PMID:29440555 1617552 Cfap418 cilia and flagella associated protein 418 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20180607 MGI PMID:29440555 1617552 Cfap418 cilia and flagella associated protein 418 gene MP:0012147 increased a-wave implicit time IAGP N RGD:5509061 20180607 MGI PMID:29440555 1617552 Cfap418 cilia and flagella associated protein 418 gene MP:0012150 increased b-wave implicit time IAGP N RGD:5509061 20180607 MGI PMID:29440555 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:21518954 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21518954 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21518954 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:21518954 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21518954 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0001237 enlarged spinous cells IAGP N RGD:5509061 20141003 MGI PMID:16192310 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:16192310 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:16192310 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:9843504 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:9843504 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:16192310 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21518954 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:21518954 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:16192310 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20160512 MGI PMID:17637742 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0008802 abnormal intestinal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21518954 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0009476 enlarged cecum IAGP N RGD:5509061 20141003 MGI PMID:21518954 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20160512 MGI PMID:17637742 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21518954 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:21518954 1617553 Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene MP:0013958 decreased small intestine length IAGP N RGD:5509061 20160304 MGI PMID:21518954 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22579044 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22579044 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20171026 MGI PMID:22802351 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20220623 MGI PMID:35477763 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20171026 MGI PMID:22802351 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22579044 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:22579044 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0001785 edema IAGP N RGD:5509061 20171026 MGI PMID:22802351 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20171026 MGI PMID:22802351 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0001914 hemorrhage IAGP N RGD:5509061 20171026 MGI PMID:22802351 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:22579044 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:22579044 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20220623 MGI PMID:35477763 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22579044 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:22579044 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20171026 MGI PMID:22802351 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20171026 MGI PMID:22802351 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20220623 MGI PMID:35477763 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20220623 MGI PMID:35477763 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20220623 MGI PMID:35477763 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20220623 MGI PMID:35477763 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0008402 increased cellular sensitivity to alkylating agents IAGP N RGD:5509061 20141003 MGI PMID:22579044 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:22579044 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20171026 MGI PMID:22802351 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:22579044 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20220623 MGI PMID:35477763 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0010770 preweaning lethality IAGP N RGD:5509061 20141003 MGI PMID:22579044 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20171026 MGI PMID:22802351 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20220623 MGI PMID:35477763 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20171026 MGI PMID:22802351 1617554 Rnaseh2b ribonuclease H2, subunit B gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20171026 MGI PMID:22802351 1617559 D16Ertd472e DNA segment, Chr 16, ERATO Doi 472, expressed gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1617559 D16Ertd472e DNA segment, Chr 16, ERATO Doi 472, expressed gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1617559 D16Ertd472e DNA segment, Chr 16, ERATO Doi 472, expressed gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20201022 MGI 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0001255 decreased body height IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0003109 short femur IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0013616 decreased volumetric bone mineral density IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617561 Scube2 signal peptide, CUB domain, EGF-like 2 gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20160602 MGI PMID:25639508 1617562 Mllt11 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 11 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20230413 MGI PMID:35379703 1617562 Mllt11 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 11 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20230413 MGI PMID:35379703 1617562 Mllt11 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 11 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20230413 MGI PMID:35379703 1617562 Mllt11 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 11 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20230413 MGI PMID:35379703 1617562 Mllt11 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 11 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20230413 MGI PMID:35379703 1617562 Mllt11 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 11 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20230413 MGI PMID:35379703 1617562 Mllt11 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 11 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20230413 MGI PMID:35379703 1617562 Mllt11 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 11 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20230413 MGI PMID:35379703 1617562 Mllt11 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 11 gene MP:0020337 abnormal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20230413 MGI PMID:35379703 1617562 Mllt11 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 11 gene MP:0021090 abnormal dendrite arborization pattern IAGP N RGD:5509061 20230413 MGI PMID:35379703 1617563 Med20 mediator complex subunit 20 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1617563 Med20 mediator complex subunit 20 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20200310 MGI 1617563 Med20 mediator complex subunit 20 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20240613 MGI PMID:30571656 1617563 Med20 mediator complex subunit 20 gene MP:0003693 abnormal blastocyst hatching IAGP N RGD:5509061 20240613 MGI PMID:30571656 1617563 Med20 mediator complex subunit 20 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20240613 MGI PMID:30571656 1617563 Med20 mediator complex subunit 20 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20240613 MGI PMID:30571656 1617563 Med20 mediator complex subunit 20 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20240613 MGI PMID:30571656 1617563 Med20 mediator complex subunit 20 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20240801 MGI PMID:30571656 1617563 Med20 mediator complex subunit 20 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1617563 Med20 mediator complex subunit 20 gene MP:0011184 absent embryonic epiblast IEA N RGD:5509061 20200310 MGI 1617563 Med20 mediator complex subunit 20 gene MP:0011185 absent primitive endoderm IEA N RGD:5509061 20200310 MGI 1617563 Med20 mediator complex subunit 20 gene MP:0012102 absent trophectoderm IEA N RGD:5509061 20200310 MGI 1617563 Med20 mediator complex subunit 20 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:17081783 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:22308309 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:17081783 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:17081783 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20200310 MGI PMID:17081783 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20200310 MGI PMID:15477348 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20200310 MGI PMID:15477350 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:17081783 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:17081783 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:22308309 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200310 MGI PMID:17081783 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20200310 MGI PMID:17081783 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:17081783 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20200310 MGI PMID:17081783 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200310 MGI PMID:17918199 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:17081783 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:17081783 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20200310 MGI PMID:22308309 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20200310 MGI PMID:22308309 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:22308309 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20200310 MGI PMID:22308309 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20200310 MGI PMID:22308309 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20200310 MGI PMID:22308309 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20200310 MGI PMID:22308309 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20200310 MGI PMID:22308309 1617564 Lat2 linker for activation of T cells family, member 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:22308309 1617566 Rnf14 ring finger protein 14 gene MP:0000162 lordosis IEA N RGD:5509061 20210128 MGI 1617566 Rnf14 ring finger protein 14 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1617566 Rnf14 ring finger protein 14 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 1617566 Rnf14 ring finger protein 14 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1617566 Rnf14 ring finger protein 14 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20210520 MGI 1617566 Rnf14 ring finger protein 14 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20231207 MGI 1617567 Krt71 keratin 71 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1617567 Krt71 keratin 71 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:14573483 1617567 Krt71 keratin 71 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:14632181 1617567 Krt71 keratin 71 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:12399393 1617567 Krt71 keratin 71 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:14573483 1617567 Krt71 keratin 71 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:17143583 1617567 Krt71 keratin 71 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:14632181 1617567 Krt71 keratin 71 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:12399393 1617567 Krt71 keratin 71 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:14573483 1617567 Krt71 keratin 71 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:14573483 1617567 Krt71 keratin 71 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:14573483 1617567 Krt71 keratin 71 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:14632181 1617567 Krt71 keratin 71 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:17143583 1617567 Krt71 keratin 71 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20111116 MGI 1617567 Krt71 keratin 71 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1617567 Krt71 keratin 71 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20141003 MGI 1617567 Krt71 keratin 71 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:14632181 1617567 Krt71 keratin 71 gene MP:0003811 abnormal hair cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:14632181 1617567 Krt71 keratin 71 gene MP:0003849 greasy coat IAGP N RGD:5509061 20141003 MGI PMID:14573483 1617567 Krt71 keratin 71 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:14573483 1617567 Krt71 keratin 71 gene MP:0009457 whorled hair IEA N RGD:5509061 20111116 MGI 1617567 Krt71 keratin 71 gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:14573483 1617567 Krt71 keratin 71 gene MP:0010202 focal dorsal hair loss IAGP N RGD:5509061 20141003 MGI PMID:14632181 1617567 Krt71 keratin 71 gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:14573483 1617567 Krt71 keratin 71 gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:14632181 1617567 Krt71 keratin 71 gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:17143583 1617568 Ranbp9 RAN binding protein 9 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0001147 small testis IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0001925 male infertility IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220714 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0004930 small epididymis IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0005159 azoospermia IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0009248 small caput epididymis IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20160128 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:21561988 1617568 Ranbp9 RAN binding protein 9 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:25474150 1617568 Ranbp9 RAN binding protein 9 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220714 MGI PMID:25474150 1617570 Snx3 sorting nexin 3 gene MP:0000111 cleft palate IEA N RGD:5509061 20210520 MGI 1617570 Snx3 sorting nexin 3 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20181227 MGI 1617570 Snx3 sorting nexin 3 gene MP:0000564 syndactyly IEA N RGD:5509061 20210520 MGI 1617570 Snx3 sorting nexin 3 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20181227 MGI 1617570 Snx3 sorting nexin 3 gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20181227 MGI 1617570 Snx3 sorting nexin 3 gene MP:0000897 abnormal midbrain morphology IEA N RGD:5509061 20181227 MGI 1617570 Snx3 sorting nexin 3 gene MP:0000914 exencephaly IEA N RGD:5509061 20210520 MGI 1617570 Snx3 sorting nexin 3 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1617570 Snx3 sorting nexin 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1617570 Snx3 sorting nexin 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1617570 Snx3 sorting nexin 3 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1617570 Snx3 sorting nexin 3 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20181227 MGI 1617570 Snx3 sorting nexin 3 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20181227 MGI 1617570 Snx3 sorting nexin 3 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 1617570 Snx3 sorting nexin 3 gene MP:0003054 spina bifida IEA N RGD:5509061 20210520 MGI 1617570 Snx3 sorting nexin 3 gene MP:0003717 pallor IEA N RGD:5509061 20181227 MGI 1617570 Snx3 sorting nexin 3 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20181227 MGI 1617570 Snx3 sorting nexin 3 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20181227 MGI 1617570 Snx3 sorting nexin 3 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210520 MGI 1617570 Snx3 sorting nexin 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1617570 Snx3 sorting nexin 3 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20181227 MGI 1617571 Rnf5 ring finger protein 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200514 MGI 1617571 Rnf5 ring finger protein 5 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20200514 MGI 1617571 Rnf5 ring finger protein 5 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20200514 MGI 1617571 Rnf5 ring finger protein 5 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:18270596 1617571 Rnf5 ring finger protein 5 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20220519 MGI 1617571 Rnf5 ring finger protein 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20200514 MGI 1617571 Rnf5 ring finger protein 5 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20200514 MGI 1617571 Rnf5 ring finger protein 5 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20200514 MGI 1617571 Rnf5 ring finger protein 5 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0000023 abnormal ear position IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0000023 abnormal ear position IAGP N RGD:5509061 20141003 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0000088 short mandible IAGP N RGD:5509061 20171026 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20160128 MGI 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0003840 abnormal coronal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0008969 abnormal nasolacrimal duct morphology IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0008969 abnormal nasolacrimal duct morphology IAGP N RGD:5509061 20141003 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0009974 decreased cerebral cortex pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20160609 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20160609 MGI PMID:21804188 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10821753 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20160128 MGI 1617572 Kat6b K(lysine) acetyltransferase 6B gene MP:0011504 abnormal limb long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21804188 1617573 Copg1 coatomer protein complex, subunit gamma 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20240328 MGI PMID:33529166 1617573 Copg1 coatomer protein complex, subunit gamma 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1617573 Copg1 coatomer protein complex, subunit gamma 1 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20160804 MGI 1617573 Copg1 coatomer protein complex, subunit gamma 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1617573 Copg1 coatomer protein complex, subunit gamma 1 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20240328 MGI PMID:33529166 1617573 Copg1 coatomer protein complex, subunit gamma 1 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20240328 MGI PMID:33529166 1617573 Copg1 coatomer protein complex, subunit gamma 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20240328 MGI PMID:33529166 1617573 Copg1 coatomer protein complex, subunit gamma 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20240328 MGI PMID:33529166 1617573 Copg1 coatomer protein complex, subunit gamma 1 gene MP:0020174 abnormal IgG level IAGP N RGD:5509061 20240328 MGI PMID:33529166 1617573 Copg1 coatomer protein complex, subunit gamma 1 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20240328 MGI PMID:33529166 1617575 Cks1b CDC28 protein kinase 1b gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17464290 1617575 Cks1b CDC28 protein kinase 1b gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11463388 1617575 Cks1b CDC28 protein kinase 1b gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17464290 1617575 Cks1b CDC28 protein kinase 1b gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17464290 1617575 Cks1b CDC28 protein kinase 1b gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17464290 1617575 Cks1b CDC28 protein kinase 1b gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17464290 1617575 Cks1b CDC28 protein kinase 1b gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17464290 1617575 Cks1b CDC28 protein kinase 1b gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:11463388 1617575 Cks1b CDC28 protein kinase 1b gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17464290 1617576 Gipc2 GIPC PDZ domain containing family, member 2 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20170511 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20170518 MGI PMID:27701470 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20170511 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20170518 MGI PMID:27701470 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20170518 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20170518 MGI PMID:27701470 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20170511 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20170511 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20170518 MGI PMID:27701470 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20170511 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20170518 MGI PMID:27701470 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20200310 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20170518 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20141003 MGI 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20170518 MGI PMID:27701470 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20170511 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0008921 increased neurotransmitter release IAGP N RGD:5509061 20170511 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20170511 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20170511 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20170518 MGI PMID:27701470 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20170511 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20170511 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20141003 MGI 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0012006 abnormal hippocampus physiology IAGP N RGD:5509061 20170511 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20170511 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0020335 abnormal dentate gyrus neuron dendrite morphology IAGP N RGD:5509061 20170511 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20170518 MGI PMID:27701470 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20170518 MGI PMID:27701470 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0020507 increased dendritic spine density IAGP N RGD:5509061 20211014 MGI PMID:26619789 1617577 Rbfox3 RNA binding protein, fox-1 homolog (C. elegans) 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:26619789 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0001263 weight loss IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0002083 premature death IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0003067 decreased liver copper level IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0010244 decreased kidney copper level IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617578 Sco1 SCO1 cytochrome c oxidase assembly protein gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20160421 MGI PMID:25683716 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617579 Lair1 leukocyte-associated Ig-like receptor 1 gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22156345 1617583 Pnrc2 proline-rich nuclear receptor coactivator 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17971453 1617583 Pnrc2 proline-rich nuclear receptor coactivator 2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:17971453 1617583 Pnrc2 proline-rich nuclear receptor coactivator 2 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:17971453 1617583 Pnrc2 proline-rich nuclear receptor coactivator 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17971453 1617583 Pnrc2 proline-rich nuclear receptor coactivator 2 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17971453 1617583 Pnrc2 proline-rich nuclear receptor coactivator 2 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17971453 1617583 Pnrc2 proline-rich nuclear receptor coactivator 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17971453 1617583 Pnrc2 proline-rich nuclear receptor coactivator 2 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17971453 1617583 Pnrc2 proline-rich nuclear receptor coactivator 2 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17971453 1617583 Pnrc2 proline-rich nuclear receptor coactivator 2 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17971453 1617583 Pnrc2 proline-rich nuclear receptor coactivator 2 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17971453 1617583 Pnrc2 proline-rich nuclear receptor coactivator 2 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:17971453 1617583 Pnrc2 proline-rich nuclear receptor coactivator 2 gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20180125 MGI PMID:17971453 1617583 Pnrc2 proline-rich nuclear receptor coactivator 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:17971453 1617584 Rufy3 RUN and FYVE domain containing 3 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20170105 MGI 1617584 Rufy3 RUN and FYVE domain containing 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20180322 MGI PMID:29089386 1617584 Rufy3 RUN and FYVE domain containing 3 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20180322 MGI PMID:29089386 1617584 Rufy3 RUN and FYVE domain containing 3 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20180322 MGI PMID:29089386 1617584 Rufy3 RUN and FYVE domain containing 3 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20180322 MGI PMID:29089386 1617584 Rufy3 RUN and FYVE domain containing 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180322 MGI PMID:29089386 1617584 Rufy3 RUN and FYVE domain containing 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1617584 Rufy3 RUN and FYVE domain containing 3 gene MP:0020581 abnormal neuron polarity IAGP N RGD:5509061 20180524 MGI PMID:29089386 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20210506 MGI PMID:32492416 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20210506 MGI PMID:32492416 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20210506 MGI PMID:32492416 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0008097 increased plasma cell number IEA N RGD:5509061 20201231 MGI 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20210506 MGI PMID:32492416 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20210506 MGI PMID:32492416 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20210506 MGI PMID:32492416 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0009617 decreased brain zinc level IAGP N RGD:5509061 20210506 MGI PMID:32492416 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0009923 decreased transitional stage T1 B cell number IEA N RGD:5509061 20201231 MGI 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20210506 MGI PMID:32492416 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0012315 impaired learning IAGP N RGD:5509061 20210506 MGI PMID:32492416 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0013430 increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20210506 MGI PMID:32492416 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20210506 MGI PMID:32492416 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20210506 MGI PMID:32492416 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0020511 decreased dendritic spine length IAGP N RGD:5509061 20210506 MGI PMID:32492416 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20210506 MGI PMID:32492416 1617585 Cttnbp2 cortactin binding protein 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:32492416 1617588 Cep63 centrosomal protein 63 gene MP:0000433 microcephaly IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0001147 small testis IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0001925 male infertility IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0004025 polyploidy IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0005159 azoospermia IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0012504 increased forebrain apoptosis IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617588 Cep63 centrosomal protein 63 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20170209 MGI PMID:26158450 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15254230 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24449270 1617589 Tinf2 Terf1 (TRF1)-interacting nuclear factor 2 gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:24449270 1617591 Mydgf myeloid derived growth factor gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20151008 MGI PMID:25581518 1617591 Mydgf myeloid derived growth factor gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20151008 MGI PMID:25581518 1617591 Mydgf myeloid derived growth factor gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20151008 MGI PMID:25581518 1617591 Mydgf myeloid derived growth factor gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210520 MGI 1617593 Med14 mediator complex subunit 14 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20150226 MGI PMID:23118208 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20150226 MGI PMID:23118208 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20150226 MGI PMID:23118208 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20150226 MGI PMID:23118208 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0006431 abnormal fibrocartilage morphology IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0008620 increased circulating interleukin-23 level IAGP N RGD:5509061 20151112 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0013942 enthesitis IAGP N RGD:5509061 20160310 MGI PMID:18204462 1617594 Clec4a2 C-type lectin domain family 4, member a2 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:18204462 1617595 B3galt2 UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 2 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20220811 MGI 1617595 B3galt2 UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20111116 MGI 1617595 B3galt2 UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 2 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20111116 MGI 1617595 B3galt2 UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1617595 B3galt2 UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 2 gene MP:0001405 impaired coordination IEA N RGD:5509061 20111116 MGI 1617595 B3galt2 UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20111116 MGI 1617595 B3galt2 UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1617595 B3galt2 UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 2 gene MP:0002989 small kidney IEA N RGD:5509061 20181227 MGI 1617595 B3galt2 UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 2 gene MP:0003064 decreased coping response IEA N RGD:5509061 20111116 MGI 1617595 B3galt2 UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 1617595 B3galt2 UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1617595 B3galt2 UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1617595 B3galt2 UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 2 gene MP:0031391 increased locomotor activity IEA N RGD:5509061 20220421 MGI 1617596 Tead4 TEA domain family member 4 gene MP:0001714 absent trophoblast giant cells IAGP N RGD:5509061 20141003 MGI PMID:17913785 1617596 Tead4 TEA domain family member 4 gene MP:0001714 absent trophoblast giant cells IAGP N RGD:5509061 20141003 MGI PMID:18083014 1617596 Tead4 TEA domain family member 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17913785 1617596 Tead4 TEA domain family member 4 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:17913785 1617596 Tead4 TEA domain family member 4 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:18083014 1617596 Tead4 TEA domain family member 4 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:18083014 1617596 Tead4 TEA domain family member 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17913785 1617596 Tead4 TEA domain family member 4 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18083014 1617596 Tead4 TEA domain family member 4 gene MP:0012058 abnormal morula morphology IAGP N RGD:5509061 20141003 MGI PMID:17913785 1617596 Tead4 TEA domain family member 4 gene MP:0012102 absent trophectoderm IAGP N RGD:5509061 20141003 MGI PMID:18083014 1617601 Cripto cripto, EGF-CFC family member gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18268105 1617601 Cripto cripto, EGF-CFC family member gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9790191 1617601 Cripto cripto, EGF-CFC family member gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:16291788 1617601 Cripto cripto, EGF-CFC family member gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:9790191 1617601 Cripto cripto, EGF-CFC family member gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:18268105 1617601 Cripto cripto, EGF-CFC family member gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:9790191 1617601 Cripto cripto, EGF-CFC family member gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9790191 1617601 Cripto cripto, EGF-CFC family member gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:16291788 1617601 Cripto cripto, EGF-CFC family member gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:9790191 1617601 Cripto cripto, EGF-CFC family member gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:18268105 1617601 Cripto cripto, EGF-CFC family member gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:9790191 1617601 Cripto cripto, EGF-CFC family member gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:18268105 1617601 Cripto cripto, EGF-CFC family member gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20220602 MGI PMID:33590845 1617601 Cripto cripto, EGF-CFC family member gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18268105 1617601 Cripto cripto, EGF-CFC family member gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220602 MGI PMID:33590845 1617601 Cripto cripto, EGF-CFC family member gene MP:0001926 female infertility IAGP N RGD:5509061 20220602 MGI PMID:33590845 1617601 Cripto cripto, EGF-CFC family member gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220602 MGI PMID:33590845 1617601 Cripto cripto, EGF-CFC family member gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16291788 1617601 Cripto cripto, EGF-CFC family member gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:18268105 1617601 Cripto cripto, EGF-CFC family member gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:18268105 1617601 Cripto cripto, EGF-CFC family member gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16291788 1617601 Cripto cripto, EGF-CFC family member gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:18268105 1617601 Cripto cripto, EGF-CFC family member gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220602 MGI PMID:33590845 1617601 Cripto cripto, EGF-CFC family member gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20220602 MGI PMID:33590845 1617601 Cripto cripto, EGF-CFC family member gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9790191 1617601 Cripto cripto, EGF-CFC family member gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0004388 absent prechordal plate IAGP N RGD:5509061 20141003 MGI PMID:16291788 1617601 Cripto cripto, EGF-CFC family member gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:16291788 1617601 Cripto cripto, EGF-CFC family member gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:16291788 1617601 Cripto cripto, EGF-CFC family member gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:18241853 1617601 Cripto cripto, EGF-CFC family member gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9790191 1617601 Cripto cripto, EGF-CFC family member gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:18268105 1617601 Cripto cripto, EGF-CFC family member gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:9790191 1617601 Cripto cripto, EGF-CFC family member gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0009094 abnormal endometrial gland morphology IAGP N RGD:5509061 20220602 MGI PMID:33590845 1617601 Cripto cripto, EGF-CFC family member gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:16291788 1617601 Cripto cripto, EGF-CFC family member gene MP:0009360 endometrium inflammation IAGP N RGD:5509061 20220602 MGI PMID:33590845 1617601 Cripto cripto, EGF-CFC family member gene MP:0009649 delayed embryo implantation IAGP N RGD:5509061 20220602 MGI PMID:33590845 1617601 Cripto cripto, EGF-CFC family member gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20220602 MGI PMID:33590845 1617601 Cripto cripto, EGF-CFC family member gene MP:0009663 abnormal uterine-embryonic axis IAGP N RGD:5509061 20220602 MGI PMID:33590845 1617601 Cripto cripto, EGF-CFC family member gene MP:0009664 abnormal luminal closure IAGP N RGD:5509061 20220602 MGI PMID:33590845 1617601 Cripto cripto, EGF-CFC family member gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20220602 MGI PMID:33590845 1617601 Cripto cripto, EGF-CFC family member gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18268105 1617601 Cripto cripto, EGF-CFC family member gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9790191 1617601 Cripto cripto, EGF-CFC family member gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9790191 1617601 Cripto cripto, EGF-CFC family member gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0011256 abnormal neural fold morphology IAGP N RGD:5509061 20141003 MGI PMID:18268105 1617601 Cripto cripto, EGF-CFC family member gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:16291788 1617601 Cripto cripto, EGF-CFC family member gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:16291788 1617601 Cripto cripto, EGF-CFC family member gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:16291788 1617601 Cripto cripto, EGF-CFC family member gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:16291788 1617601 Cripto cripto, EGF-CFC family member gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:9876177 1617601 Cripto cripto, EGF-CFC family member gene MP:0013185 absent anterior definitive endoderm IAGP N RGD:5509061 20141003 MGI PMID:16291788 1617602 Tdg thymine DNA glycosylase gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21278727 1617602 Tdg thymine DNA glycosylase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0004181 abnormal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0009797 abnormal mismatch repair IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0010500 myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617602 Tdg thymine DNA glycosylase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21278727 1617602 Tdg thymine DNA glycosylase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21722948 1617604 Sema6a sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11242070 1617604 Sema6a sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:21270798 1617604 Sema6a sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20484647 1617604 Sema6a sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:18327254 1617604 Sema6a sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:24179230 1617604 Sema6a sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:24179230 1617604 Sema6a sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24179230 1617604 Sema6a sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21270798 1617604 Sema6a sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24179230 1617604 Sema6a sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21270798 1617604 Sema6a sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:24179230 1617604 Sema6a sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:21270798 1617605 Sema3e sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20230119 MGI 1617605 Sema3e sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19421194 1617605 Sema3e sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:19421194 1617605 Sema3e sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 1617605 Sema3e sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20230119 MGI 1617605 Sema3e sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:21505259 1617605 Sema3e sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20230119 MGI 1617605 Sema3e sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:15550623 1617605 Sema3e sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21505259 1617605 Sema3e sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:24210822 1617605 Sema3e sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E gene MP:0006241 abnormal placement of pupils IEA N RGD:5509061 20230119 MGI 1617605 Sema3e sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20230119 MGI 1617605 Sema3e sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230119 MGI 1617605 Sema3e sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15550623 1617605 Sema3e sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E gene MP:0012539 Bergmeister's papilla IEA N RGD:5509061 20141003 MGI 1617607 Cavin2 caveolae associated 2 gene MP:0003180 abnormal pulmonary endothelial cell surface IAGP N RGD:5509061 20141003 MGI PMID:23652019 1617607 Cavin2 caveolae associated 2 gene MP:0003950 abnormal plasma membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:23652019 1617607 Cavin2 caveolae associated 2 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23652019 1617607 Cavin2 caveolae associated 2 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23652019 1617607 Cavin2 caveolae associated 2 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23652019 1617608 Cxcl15 C-X-C motif chemokine ligand 15 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11207292 1617608 Cxcl15 C-X-C motif chemokine ligand 15 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11207292 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18443297 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9606187 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:9606187 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:18448676 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9606187 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18443297 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15483626 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0001379 abnormal penile erection IAGP N RGD:5509061 20141003 MGI PMID:10688876 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12853418 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18443297 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19952371 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:14568994 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10688876 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17901360 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17901360 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11786513 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17901360 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11786513 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18443297 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:18443297 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:18443297 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18448676 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22245782 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18443297 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11786513 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:10688876 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:9606187 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20181227 MGI 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20141003 MGI PMID:23535651 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20141003 MGI PMID:9606187 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0003307 pyloric stenosis IAGP N RGD:5509061 20141003 MGI PMID:9606187 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:22245782 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:9606187 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0004216 salt-resistant hypertension IAGP N RGD:5509061 20141003 MGI PMID:18448676 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17901360 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18448676 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22245782 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9606187 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19952371 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:18443297 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:18443297 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:18448676 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:22245782 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:17901360 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:9606187 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:17901360 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:23535651 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:9606187 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18448676 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22245782 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18448676 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22245782 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:19952371 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0010035 increased erythrocyte clearance IAGP N RGD:5509061 20141003 MGI PMID:18443297 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:18443297 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0010781 pyloric sphincter hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9606187 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0010786 stomach fundus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9606187 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0011015 decreased body surface temperature IAGP N RGD:5509061 20141003 MGI PMID:19952371 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0011082 abnormal gastrointestinal motility IAGP N RGD:5509061 20141003 MGI PMID:23535651 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0011085 postnatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20141003 MGI PMID:19952371 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:19952371 1617610 Prkg1 protein kinase, cGMP-dependent, type I gene MP:0014396 decreased fat cell mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:19952371 1617611 Prim1 DNA primase, p49 subunit gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1617611 Prim1 DNA primase, p49 subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1617611 Prim1 DNA primase, p49 subunit gene MP:0011185 absent primitive endoderm IEA N RGD:5509061 20191205 MGI 1617611 Prim1 DNA primase, p49 subunit gene MP:0012102 absent trophectoderm IEA N RGD:5509061 20191205 MGI 1617611 Prim1 DNA primase, p49 subunit gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1617611 Prim1 DNA primase, p49 subunit gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240801 MGI 1617613 Med1 mediator complex subunit 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:14500757 1617613 Med1 mediator complex subunit 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14500757 1617613 Med1 mediator complex subunit 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:14500757 1617613 Med1 mediator complex subunit 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14500757 1617613 Med1 mediator complex subunit 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15150259 1617613 Med1 mediator complex subunit 1 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:20351249 1617613 Med1 mediator complex subunit 1 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:20351249 1617613 Med1 mediator complex subunit 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20210422 MGI 1617613 Med1 mediator complex subunit 1 gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:14500757 1617613 Med1 mediator complex subunit 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:10747854 1617613 Med1 mediator complex subunit 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221103 MGI 1617613 Med1 mediator complex subunit 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10747854 1617613 Med1 mediator complex subunit 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10747854 1617613 Med1 mediator complex subunit 1 gene MP:0001722 pale yolk sac IEA N RGD:5509061 20221103 MGI 1617613 Med1 mediator complex subunit 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10747854 1617613 Med1 mediator complex subunit 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20190502 MGI 1617613 Med1 mediator complex subunit 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:14500757 1617613 Med1 mediator complex subunit 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:10747854 1617613 Med1 mediator complex subunit 1 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:10747854 1617613 Med1 mediator complex subunit 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0003542 abnormal vascular endothelial cell development IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0003717 pallor IEA N RGD:5509061 20221103 MGI 1617613 Med1 mediator complex subunit 1 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10747854 1617613 Med1 mediator complex subunit 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14500757 1617613 Med1 mediator complex subunit 1 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10747854 1617613 Med1 mediator complex subunit 1 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20221103 MGI 1617613 Med1 mediator complex subunit 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210422 MGI 1617613 Med1 mediator complex subunit 1 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10747854 1617613 Med1 mediator complex subunit 1 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0006062 abnormal vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0006372 impaired placental function IAGP N RGD:5509061 20141003 MGI PMID:14500757 1617613 Med1 mediator complex subunit 1 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0008253 absent megakaryocytes IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0008253 absent megakaryocytes IAGP N RGD:5509061 20141003 MGI PMID:14500757 1617613 Med1 mediator complex subunit 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10747854 1617613 Med1 mediator complex subunit 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14500757 1617613 Med1 mediator complex subunit 1 gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20351249 1617613 Med1 mediator complex subunit 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20210422 MGI 1617613 Med1 mediator complex subunit 1 gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20160317 MGI PMID:20351249 1617613 Med1 mediator complex subunit 1 gene MP:0010500 myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11724781 1617613 Med1 mediator complex subunit 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10747854 1617613 Med1 mediator complex subunit 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14500757 1617613 Med1 mediator complex subunit 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210422 MGI 1617613 Med1 mediator complex subunit 1 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:10882104 1617613 Med1 mediator complex subunit 1 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0012270 cardiac edema IAGP N RGD:5509061 20171026 MGI PMID:27548259 1617613 Med1 mediator complex subunit 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 1617613 Med1 mediator complex subunit 1 gene MP:0014390 decreased myocardial fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:27548259 1617614 Endou endonuclease, polyU-specific gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1617614 Endou endonuclease, polyU-specific gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:24344237 1617614 Endou endonuclease, polyU-specific gene MP:0010675 decreased activation-induced B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24344237 1617617 Mt2 metallothionein 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10869470 1617617 Mt2 metallothionein 2 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:10869470 1617617 Mt2 metallothionein 2 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10087067 1617617 Mt2 metallothionein 2 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10947810 1617617 Mt2 metallothionein 2 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11585628 1617617 Mt2 metallothionein 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16166738 1617617 Mt2 metallothionein 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:8290567 1617617 Mt2 metallothionein 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:10966523 1617617 Mt2 metallothionein 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10087053 1617617 Mt2 metallothionein 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10906280 1617617 Mt2 metallothionein 2 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10906280 1617617 Mt2 metallothionein 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10869470 1617617 Mt2 metallothionein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8640230 1617617 Mt2 metallothionein 2 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:8290567 1617617 Mt2 metallothionein 2 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:10087053 1617617 Mt2 metallothionein 2 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:8290567 1617617 Mt2 metallothionein 2 gene MP:0001670 abnormal intestinal mineral absorption IAGP N RGD:5509061 20141003 MGI PMID:9566988 1617617 Mt2 metallothionein 2 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:10966523 1617617 Mt2 metallothionein 2 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8367468 1617617 Mt2 metallothionein 2 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:10087067 1617617 Mt2 metallothionein 2 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:10906280 1617617 Mt2 metallothionein 2 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:10966523 1617617 Mt2 metallothionein 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:16166738 1617617 Mt2 metallothionein 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10087067 1617617 Mt2 metallothionein 2 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:10460198 1617617 Mt2 metallothionein 2 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:8683339 1617617 Mt2 metallothionein 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12807749 1617617 Mt2 metallothionein 2 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:16430929 1617617 Mt2 metallothionein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8290567 1617617 Mt2 metallothionein 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10087053 1617617 Mt2 metallothionein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8640230 1617617 Mt2 metallothionein 2 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10947810 1617617 Mt2 metallothionein 2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:10906280 1617617 Mt2 metallothionein 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10906280 1617617 Mt2 metallothionein 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:10947810 1617617 Mt2 metallothionein 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:10087053 1617617 Mt2 metallothionein 2 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:8290567 1617617 Mt2 metallothionein 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10869470 1617617 Mt2 metallothionein 2 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:10966523 1617617 Mt2 metallothionein 2 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:8290567 1617617 Mt2 metallothionein 2 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:10966523 1617617 Mt2 metallothionein 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10947810 1617617 Mt2 metallothionein 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11585628 1617617 Mt2 metallothionein 2 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10966523 1617617 Mt2 metallothionein 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:10087067 1617617 Mt2 metallothionein 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:11585628 1617617 Mt2 metallothionein 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:11585628 1617617 Mt2 metallothionein 2 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10087067 1617617 Mt2 metallothionein 2 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10869470 1617617 Mt2 metallothionein 2 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10906280 1617617 Mt2 metallothionein 2 gene MP:0003946 renal necrosis IAGP N RGD:5509061 20141003 MGI PMID:10966523 1617617 Mt2 metallothionein 2 gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:10947810 1617617 Mt2 metallothionein 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:10947810 1617617 Mt2 metallothionein 2 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15618127 1617617 Mt2 metallothionein 2 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:10869470 1617617 Mt2 metallothionein 2 gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10966523 1617617 Mt2 metallothionein 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:10087053 1617617 Mt2 metallothionein 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:10426817 1617617 Mt2 metallothionein 2 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:11585628 1617617 Mt2 metallothionein 2 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:10966523 1617617 Mt2 metallothionein 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:10906280 1617617 Mt2 metallothionein 2 gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:10966523 1617617 Mt2 metallothionein 2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10906280 1617617 Mt2 metallothionein 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10906280 1617617 Mt2 metallothionein 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10906280 1617617 Mt2 metallothionein 2 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:10764993 1617617 Mt2 metallothionein 2 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16936113 1617617 Mt2 metallothionein 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:8683339 1617617 Mt2 metallothionein 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:10087067 1617617 Mt2 metallothionein 2 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:15618127 1617617 Mt2 metallothionein 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:10966523 1617617 Mt2 metallothionein 2 gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20141003 MGI PMID:10869470 1617617 Mt2 metallothionein 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10906280 1617617 Mt2 metallothionein 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10906280 1617617 Mt2 metallothionein 2 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:10906280 1617617 Mt2 metallothionein 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:11585628 1617617 Mt2 metallothionein 2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:11585628 1617617 Mt2 metallothionein 2 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:11585628 1617617 Mt2 metallothionein 2 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10426817 1617617 Mt2 metallothionein 2 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10966523 1617617 Mt2 metallothionein 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10087053 1617617 Mt2 metallothionein 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10869470 1617617 Mt2 metallothionein 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10947810 1617617 Mt2 metallothionein 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10966523 1617617 Mt2 metallothionein 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16936113 1617617 Mt2 metallothionein 2 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:8640230 1617617 Mt2 metallothionein 2 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:10966523 1617617 Mt2 metallothionein 2 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10413187 1617617 Mt2 metallothionein 2 gene MP:0009615 abnormal zinc homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10460198 1617617 Mt2 metallothionein 2 gene MP:0009615 abnormal zinc homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10947810 1617617 Mt2 metallothionein 2 gene MP:0009615 abnormal zinc homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8683339 1617617 Mt2 metallothionein 2 gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:10966523 1617617 Mt2 metallothionein 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10087053 1617617 Mt2 metallothionein 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16166738 1617617 Mt2 metallothionein 2 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:10869470 1617617 Mt2 metallothionein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8640230 1617617 Mt2 metallothionein 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8640230 1617617 Mt2 metallothionein 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8640230 1617617 Mt2 metallothionein 2 gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:8683339 1617617 Mt2 metallothionein 2 gene MP:0011924 abnormal liver zinc level IAGP N RGD:5509061 20170223 MGI PMID:8683339 1617617 Mt2 metallothionein 2 gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20160428 MGI PMID:10087067 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:9864150 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10446263 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10446263 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:9376320 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:9376320 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9376320 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:12915229 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:9376320 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:12915229 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:12915229 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9376320 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:10446263 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0001257 increased body length IEA N RGD:5509061 20160804 MGI 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9864150 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:9376320 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10446263 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:7758946 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:9376320 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:9626493 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9376320 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9376320 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9626493 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9864150 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10446263 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16900512 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:10446263 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11301191 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:10446263 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:7758946 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15870077 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:7758946 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:7758946 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:9626493 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:10446263 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0004032 abnormal interventricular groove morphology IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0004062 dilated heart right atrium IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9376320 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:7758946 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20160804 MGI 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10446263 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:9376320 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:9376320 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10807864 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10446263 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9376320 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7758946 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7758946 1617619 Jarid2 jumonji and AT-rich interaction domain containing 2 gene MP:0011243 decreased fetal derived definitive erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9864150 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0000743 muscle spasm IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0000938 motor neuron degeneration IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:14556008 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19436707 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:14556008 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0001523 impaired righting response IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0001922 reduced male fertility IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0002064 seizures IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14556008 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0002371 abnormal thymus cortex morphology IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0002375 abnormal thymus medulla morphology IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0002876 abnormal thyroid gland physiology IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:19436707 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0003314 dysmetria IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0004163 abnormal adenohypophysis morphology IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0004696 abnormal thyroid follicle morphology IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:14556008 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:14556008 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0008026 abnormal brain white matter morphology IEA N RGD:5509061 20111116 MGI 1617620 Atcay ataxia, cerebellar, Cayman type gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1617621 Itgb5 integrin beta 5 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20141003 MGI 1617621 Itgb5 integrin beta 5 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20141003 MGI 1617621 Itgb5 integrin beta 5 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20141003 MGI 1617621 Itgb5 integrin beta 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10629031 1617621 Itgb5 integrin beta 5 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20160804 MGI 1617621 Itgb5 integrin beta 5 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:10629031 1617621 Itgb5 integrin beta 5 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:11786903 1617621 Itgb5 integrin beta 5 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:11786903 1617623 Itgav integrin alpha V gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12370313 1617623 Itgav integrin alpha V gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12370313 1617623 Itgav integrin alpha V gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18451854 1617623 Itgav integrin alpha V gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:20570943 1617623 Itgav integrin alpha V gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:20570943 1617623 Itgav integrin alpha V gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:20570943 1617623 Itgav integrin alpha V gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0005502 abnormal renal/urinary system physiology IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0006052 cerebellum hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0008136 enlarged Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17895374 1617623 Itgav integrin alpha V gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15576410 1617623 Itgav integrin alpha V gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:18451854 1617623 Itgav integrin alpha V gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:20570943 1617623 Itgav integrin alpha V gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20570943 1617623 Itgav integrin alpha V gene MP:0010466 vascular ring IAGP N RGD:5509061 20141003 MGI PMID:20570943 1617623 Itgav integrin alpha V gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20570943 1617623 Itgav integrin alpha V gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12370313 1617623 Itgav integrin alpha V gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20570943 1617623 Itgav integrin alpha V gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12370313 1617623 Itgav integrin alpha V gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20141003 MGI PMID:9827803 1617623 Itgav integrin alpha V gene MP:0031154 intestinal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:9827803 1617628 Hars1 histidyl-tRNA synthetase 1 gene MP:0001967 deafness IAGP N RGD:5509061 20160929 MGI PMID:27534441 1617630 Ephb4 Eph receptor B4 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10518221 1617630 Ephb4 Eph receptor B4 gene MP:0000264 failure of vascular branching IAGP N RGD:5509061 20141003 MGI PMID:10518221 1617630 Ephb4 Eph receptor B4 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:10518221 1617630 Ephb4 Eph receptor B4 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20170209 MGI 1617630 Ephb4 Eph receptor B4 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:10518221 1617630 Ephb4 Eph receptor B4 gene MP:0000484 abnormal pulmonary artery morphology IEA N RGD:5509061 20170209 MGI 1617630 Ephb4 Eph receptor B4 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20170209 MGI 1617630 Ephb4 Eph receptor B4 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:10518221 1617630 Ephb4 Eph receptor B4 gene MP:0003411 abnormal vein development IAGP N RGD:5509061 20141003 MGI PMID:10518221 1617630 Ephb4 Eph receptor B4 gene MP:0003675 kidney cyst IEA N RGD:5509061 20170209 MGI 1617630 Ephb4 Eph receptor B4 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:10518221 1617630 Ephb4 Eph receptor B4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10518221 1617630 Ephb4 Eph receptor B4 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:10518221 1617630 Ephb4 Eph receptor B4 gene MP:0004113 abnormal aortic arch morphology IEA N RGD:5509061 20170209 MGI 1617630 Ephb4 Eph receptor B4 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:10518221 1617630 Ephb4 Eph receptor B4 gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:10518221 1617630 Ephb4 Eph receptor B4 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20170209 MGI 1617630 Ephb4 Eph receptor B4 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170209 MGI 1617630 Ephb4 Eph receptor B4 gene MP:0010466 vascular ring IEA N RGD:5509061 20170209 MGI 1617630 Ephb4 Eph receptor B4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10518221 1617631 Ephb2 Eph receptor B2 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20200310 MGI PMID:10839360 1617631 Ephb2 Eph receptor B2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20200310 MGI PMID:21539827 1617631 Ephb2 Eph receptor B2 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:16777604 1617631 Ephb2 Eph receptor B2 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1617631 Ephb2 Eph receptor B2 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20200310 MGI PMID:23143520 1617631 Ephb2 Eph receptor B2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20200310 MGI PMID:10839360 1617631 Ephb2 Eph receptor B2 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:10839360 1617631 Ephb2 Eph receptor B2 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:17158005 1617631 Ephb2 Eph receptor B2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:10839360 1617631 Ephb2 Eph receptor B2 gene MP:0001410 head bobbing IAGP N RGD:5509061 20200310 MGI PMID:10839360 1617631 Ephb2 Eph receptor B2 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1617631 Ephb2 Eph receptor B2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20200310 MGI PMID:19914164 1617631 Ephb2 Eph receptor B2 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:10839360 1617631 Ephb2 Eph receptor B2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200310 MGI PMID:12971893 1617631 Ephb2 Eph receptor B2 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:10839360 1617631 Ephb2 Eph receptor B2 gene MP:0002946 delayed axon extension IAGP N RGD:5509061 20200310 MGI PMID:10839360 1617631 Ephb2 Eph receptor B2 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20200310 MGI PMID:10839360 1617631 Ephb2 Eph receptor B2 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20200310 MGI PMID:8689685 1617631 Ephb2 Eph receptor B2 gene MP:0003052 omphalocele IAGP N RGD:5509061 20200310 MGI PMID:21539827 1617631 Ephb2 Eph receptor B2 gene MP:0003124 hypospadia IAGP N RGD:5509061 20200310 MGI PMID:15223334 1617631 Ephb2 Eph receptor B2 gene MP:0003631 nervous system phenotype IAGP N RGD:5509061 20200402 MGI PMID:8689685 1617631 Ephb2 Eph receptor B2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20200310 MGI PMID:23143520 1617631 Ephb2 Eph receptor B2 gene MP:0004267 abnormal optic tract morphology IAGP N RGD:5509061 20200310 MGI PMID:12971893 1617631 Ephb2 Eph receptor B2 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20200310 MGI PMID:10839360 1617631 Ephb2 Eph receptor B2 gene MP:0004775 abnormal vestibular dark cell morphology IAGP N RGD:5509061 20200310 MGI PMID:10839360 1617631 Ephb2 Eph receptor B2 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:16777604 1617631 Ephb2 Eph receptor B2 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20200310 MGI PMID:16777604 1617631 Ephb2 Eph receptor B2 gene MP:0004885 abnormal endolymph physiology IAGP N RGD:5509061 20200310 MGI PMID:17158005 1617631 Ephb2 Eph receptor B2 gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20200310 MGI PMID:15223334 1617631 Ephb2 Eph receptor B2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200310 MGI PMID:19182796 1617631 Ephb2 Eph receptor B2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200310 MGI PMID:21847105 1617631 Ephb2 Eph receptor B2 gene MP:0006389 abnormal vestibular endolymph physiology IAGP N RGD:5509061 20200310 MGI PMID:17158005 1617631 Ephb2 Eph receptor B2 gene MP:0006391 abnormal vestibular endolymph ionic homeostasis IAGP N RGD:5509061 20200310 MGI PMID:17158005 1617631 Ephb2 Eph receptor B2 gene MP:0008066 small endolymphatic duct IAGP N RGD:5509061 20200310 MGI PMID:10839360 1617631 Ephb2 Eph receptor B2 gene MP:0008960 abnormal axon pruning IAGP N RGD:5509061 20200310 MGI PMID:19182796 1617631 Ephb2 Eph receptor B2 gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:19914164 1617631 Ephb2 Eph receptor B2 gene MP:0010860 abnormal anterior commissure pars posterior morphology IAGP N RGD:5509061 20200310 MGI PMID:8689685 1617631 Ephb2 Eph receptor B2 gene MP:0014077 ectopic Paneth cells IAGP N RGD:5509061 20200310 MGI PMID:19914164 1617632 Eng endoglin gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1617632 Eng endoglin gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:10348742 1617632 Eng endoglin gene MP:0000265 blood vessel atresia IAGP N RGD:5509061 20141003 MGI PMID:10348742 1617632 Eng endoglin gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1617632 Eng endoglin gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10625534 1617632 Eng endoglin gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:10625534 1617632 Eng endoglin gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160623 MGI PMID:25082229 1617632 Eng endoglin gene MP:0001429 dehydration IAGP N RGD:5509061 20160623 MGI PMID:25082229 1617632 Eng endoglin gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10625534 1617632 Eng endoglin gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10625534 1617632 Eng endoglin gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20160623 MGI PMID:24520391 1617632 Eng endoglin gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17506087 1617632 Eng endoglin gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:10348742 1617632 Eng endoglin gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20210128 MGI 1617632 Eng endoglin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10348742 1617632 Eng endoglin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10625534 1617632 Eng endoglin gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210520 MGI 1617632 Eng endoglin gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20210128 MGI 1617632 Eng endoglin gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160623 MGI PMID:24520391 1617632 Eng endoglin gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0002083 premature death IAGP N RGD:5509061 20160623 MGI PMID:24520391 1617632 Eng endoglin gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1617632 Eng endoglin gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210128 MGI 1617632 Eng endoglin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15090446 1617632 Eng endoglin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17506087 1617632 Eng endoglin gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:10625534 1617632 Eng endoglin gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20220811 MGI 1617632 Eng endoglin gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1617632 Eng endoglin gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10348742 1617632 Eng endoglin gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10625534 1617632 Eng endoglin gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17506087 1617632 Eng endoglin gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10625534 1617632 Eng endoglin gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:10625534 1617632 Eng endoglin gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10625534 1617632 Eng endoglin gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0004176 ear telangiectasia IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0004177 tail telangiectasia IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0004178 neck telangiectasia IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0004181 abnormal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:10348742 1617632 Eng endoglin gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:10348742 1617632 Eng endoglin gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:10348742 1617632 Eng endoglin gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:10625534 1617632 Eng endoglin gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20160623 MGI PMID:24520391 1617632 Eng endoglin gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20160623 MGI PMID:25082229 1617632 Eng endoglin gene MP:0005036 diarrhea IAGP N RGD:5509061 20160623 MGI PMID:25082229 1617632 Eng endoglin gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:10348742 1617632 Eng endoglin gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:10625534 1617632 Eng endoglin gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10348742 1617632 Eng endoglin gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10625534 1617632 Eng endoglin gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15548578 1617632 Eng endoglin gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10348742 1617632 Eng endoglin gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20160623 MGI PMID:24520391 1617632 Eng endoglin gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20160623 MGI PMID:25082229 1617632 Eng endoglin gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:10625534 1617632 Eng endoglin gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20231221 MGI PMID:10625534 1617632 Eng endoglin gene MP:0010530 cerebral arteriovenous malformation IAGP N RGD:5509061 20141003 MGI PMID:22571958 1617632 Eng endoglin gene MP:0010531 gastrointestinal arteriovenous malformation IAGP N RGD:5509061 20160623 MGI PMID:24520391 1617632 Eng endoglin gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17506087 1617632 Eng endoglin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10348742 1617632 Eng endoglin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10625534 1617632 Eng endoglin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1617632 Eng endoglin gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10348742 1617632 Eng endoglin gene MP:0012732 abnormal perineural vascular plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:10348742 1617632 Eng endoglin gene MP:0013139 moribund IAGP N RGD:5509061 20160623 MGI PMID:25082229 1617632 Eng endoglin gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:10562296 1617632 Eng endoglin gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10594039 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0001999 photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0002208 abnormal germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:10594039 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:17287518 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12717441 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17287518 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:17287518 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12717441 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:17287518 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12717441 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004407 increased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:17287518 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004408 decreased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:17287518 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004432 abnormal cochlear hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12717441 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004432 abnormal cochlear hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17287518 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:12717441 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12717441 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004749 nonsyndromic hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12717441 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10557343 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12717441 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0013602 abnormal Leydig cell differentiation IAGP N RGD:5509061 20150319 MGI PMID:11287627 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:10594039 1617633 Cdkn2d cyclin dependent kinase inhibitor 2D gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220623 MGI PMID:10594039 1617634 Cdh4 cadherin 4 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:11839813 1617634 Cdh4 cadherin 4 gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20220519 MGI 1617634 Cdh4 cadherin 4 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20160421 MGI 1617634 Cdh4 cadherin 4 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11839813 1617634 Cdh4 cadherin 4 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:11839813 1617634 Cdh4 cadherin 4 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20220811 MGI 1617634 Cdh4 cadherin 4 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220811 MGI 1617634 Cdh4 cadherin 4 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:11839813 1617634 Cdh4 cadherin 4 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:11839813 1617634 Cdh4 cadherin 4 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:11839813 1617634 Cdh4 cadherin 4 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11839813 1617635 Cdh3 cadherin 3 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9362520 1617635 Cdh3 cadherin 3 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:9362520 1617635 Cdh3 cadherin 3 gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9362520 1617635 Cdh3 cadherin 3 gene MP:0001884 mammary gland alveolar hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9362520 1617635 Cdh3 cadherin 3 gene MP:0001885 mammary gland duct hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9362520 1617636 Cd82 CD82 antigen gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20220721 MGI PMID:35754722 1617636 Cd82 CD82 antigen gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20200310 MGI PMID:25149363 1617636 Cd82 CD82 antigen gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20220721 MGI PMID:35754722 1617636 Cd82 CD82 antigen gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20220721 MGI PMID:35754722 1617636 Cd82 CD82 antigen gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20200310 MGI PMID:25149363 1617636 Cd82 CD82 antigen gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20220721 MGI PMID:35754722 1617636 Cd82 CD82 antigen gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20200310 MGI PMID:25149363 1617636 Cd82 CD82 antigen gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20220721 MGI PMID:35754722 1617636 Cd82 CD82 antigen gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20200310 MGI PMID:25149363 1617636 Cd82 CD82 antigen gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20220721 MGI PMID:35754722 1617636 Cd82 CD82 antigen gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20200310 MGI PMID:25149363 1617636 Cd82 CD82 antigen gene MP:0012049 increased susceptilbility to retina ischemic injury IAGP N RGD:5509061 20220721 MGI PMID:35754722 1617636 Cd82 CD82 antigen gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20220721 MGI PMID:35754722 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20170314 MGI PMID:26301816 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:12097390 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:21423173 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20194438 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000599 enlarged liver IAGP N RGD:5509061 20170314 MGI PMID:26301816 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:20194438 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22891272 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170314 MGI PMID:26301816 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:22891272 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:24190965 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000692 small spleen IAGP N RGD:5509061 20190509 MGI PMID:24888588 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000692 small spleen IAGP N RGD:5509061 20240328 MGI PMID:38095286 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20170314 MGI PMID:26301816 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11857807 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21708930 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:21530328 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001577 anemia IAGP N RGD:5509061 20170314 MGI PMID:26301816 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:16860757 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:16860757 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:21708930 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:23027924 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:23942237 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11136817 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11514602 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15186779 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18329371 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19812384 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20194438 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21795747 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22431510 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24190965 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20170314 MGI PMID:26301816 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:24190965 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15186779 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22761313 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23942237 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:24190965 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20190912 MGI PMID:31088898 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20230608 MGI PMID:16860757 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:23942237 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002083 premature death IAGP N RGD:5509061 20191128 MGI PMID:22078222 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12097390 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15186779 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16782029 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16818674 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16940357 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22891272 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20151224 MGI PMID:24509509 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12097390 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11857807 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16940357 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:15004164 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002440 abnormal memory B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23027924 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:16860757 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:22302739 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20151224 MGI PMID:24509509 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20190509 MGI PMID:24888588 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20240328 MGI PMID:38095286 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16860757 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21464221 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21530328 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21708930 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21960637 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22302739 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22891272 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23109291 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20240328 MGI PMID:38095286 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20240516 MGI PMID:36803766 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:8650582 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16860757 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002491 decreased IgD level IAGP N RGD:5509061 20141003 MGI PMID:15186779 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23109291 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002493 increased IgG level IAGP N RGD:5509061 20191128 MGI PMID:22078222 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22302739 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23109291 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:23123062 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0002827 abnormal renal corpuscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22302739 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16860757 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0003134 increased late pro-B cell number IAGP N RGD:5509061 20190509 MGI PMID:24888588 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20170314 MGI PMID:26301816 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20180208 MGI PMID:25074913 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:22302739 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20191128 MGI PMID:22078222 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:16860757 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20240516 MGI PMID:36803766 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:22302739 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23109291 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20191128 MGI PMID:22078222 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:22302739 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20191128 MGI PMID:22078222 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20191128 MGI PMID:22078222 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21530328 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21464221 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:23109291 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20191128 MGI PMID:22078222 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:23027924 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:17420268 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:21464221 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22761313 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20161013 MGI PMID:23343763 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:22302739 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20191128 MGI PMID:22078222 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17420268 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20160414 MGI PMID:26832406 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004940 abnormal B-1 B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23942237 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004944 abnormal B cell negative selection IAGP N RGD:5509061 20191128 MGI PMID:22078222 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22891272 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22891272 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:24190965 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21530328 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:11514602 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15004164 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15186779 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16782029 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16940357 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18329371 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20194438 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21464221 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21708930 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22302739 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22761313 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:24190965 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8650582 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160414 MGI PMID:26832406 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170314 MGI PMID:26301816 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180208 MGI PMID:25074913 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20191128 MGI PMID:22078222 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20240328 MGI PMID:38095286 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20240627 MGI PMID:38011999 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12097390 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16860757 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21464221 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21530328 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24244019 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20161013 MGI PMID:23343763 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20240516 MGI PMID:36803766 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22302739 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20161013 MGI PMID:23343763 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20210708 MGI PMID:32868928 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16940357 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21530328 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21530328 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:22302739 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20191128 MGI PMID:22078222 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:16818674 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:16860757 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:21464221 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:21708930 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:23942237 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008169 increased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008170 decreased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:23942237 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:24244019 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:15186779 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21708930 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:22302739 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:24244019 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20190912 MGI PMID:31088898 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:22302739 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:23123062 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:23027924 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:11514602 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:15186779 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:22302739 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:24244019 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11136817 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18329371 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20151224 MGI PMID:24509509 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20190509 MGI PMID:24888588 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:16860757 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:11136817 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008191 abnormal follicular B cell physiology IAGP N RGD:5509061 20190912 MGI PMID:31088898 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21464221 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008194 abnormal memory B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008194 abnormal memory B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23027924 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008203 absent B-1a cells IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16940357 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20194438 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20151224 MGI PMID:24509509 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20180208 MGI PMID:25074913 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20240627 MGI PMID:38011999 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11136817 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11514602 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16940357 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18329371 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20194438 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20151224 MGI PMID:24509509 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20160414 MGI PMID:26832406 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20190509 MGI PMID:24888588 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20240328 MGI PMID:38095286 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11136817 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11514602 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16782029 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18329371 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22302739 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:8650582 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20160414 MGI PMID:26832406 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20190912 MGI PMID:31088898 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20240328 MGI PMID:38095286 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20240627 MGI PMID:38011999 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:11514602 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:12097390 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008213 absent immature B cells IAGP N RGD:5509061 20141003 MGI PMID:15186779 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17420268 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18329371 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21708930 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20160414 MGI PMID:26832406 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20170314 MGI PMID:26301816 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20240328 MGI PMID:38095286 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:11514602 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20240516 MGI PMID:36803766 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008233 abnormal pro-B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17420268 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008233 abnormal pro-B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18356083 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008240 abnormal spleen marginal zone macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:15004164 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008241 abnormal metallophilic macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:15004164 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20190912 MGI PMID:31088898 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20190912 MGI PMID:31088898 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11514602 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:23942237 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160414 MGI PMID:26832406 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20190912 MGI PMID:31088898 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20240627 MGI PMID:38011999 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:23942237 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20230608 MGI PMID:16860757 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:23942237 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20190912 MGI PMID:31088898 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:23942237 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20190912 MGI PMID:31088898 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20230608 MGI PMID:16860757 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:21530328 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21530328 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21530328 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:21530328 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:21464221 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008744 abnormal B cell anergy IAGP N RGD:5509061 20191128 MGI PMID:22078222 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008755 abnormal immunoglobulin V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:18329371 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20240328 MGI PMID:38095286 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008766 abnormal B cell receptor editing IAGP N RGD:5509061 20240328 MGI PMID:38095286 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20194438 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21464221 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22213803 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20160414 MGI PMID:26832406 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20210708 MGI PMID:32868928 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008896 increased IgG2c level IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20180208 MGI PMID:25074913 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20190912 MGI PMID:31088898 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20190509 MGI PMID:24888588 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:21795747 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20160414 MGI PMID:26832406 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0009922 increased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0009925 increased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21427701 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21708930 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:23955076 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0010228 decreased transitional stage T3 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21708930 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0010229 increased transitional stage T3 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21841126 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20160414 MGI PMID:26832406 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0011815 increased pre-pro B cell number IAGP N RGD:5509061 20240328 MGI PMID:38095286 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160414 MGI PMID:26832406 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0013940 abnormal plasmablast number IAGP N RGD:5509061 20190912 MGI PMID:31088898 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0014050 increased B cell acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20170314 MGI PMID:26301816 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0014403 decreased early pro-B cell number IAGP N RGD:5509061 20240405 MGI PMID:38095286 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0014404 decreased late pro-B cell number IAGP N RGD:5509061 20240405 MGI PMID:38095286 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:21464221 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:21530328 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20180215 MGI 1617637 Cd79a CD79A antigen (immunoglobulin-associated alpha) gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:22213803 1617844 Faiml Fas apoptotic inhibitory molecule like gene MP:0001147 small testis IAGP N RGD:5509061 20211021 MGI PMID:34326397 1617884 Calhm1 calcium homeostasis modulator 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1617884 Calhm1 calcium homeostasis modulator 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1617884 Calhm1 calcium homeostasis modulator 1 gene MP:0001985 abnormal gustatory system physiology IAGP N RGD:5509061 20190620 MGI PMID:29681531 1617884 Calhm1 calcium homeostasis modulator 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22711817 1617885 Cyp26c1 cytochrome P450, family 26, subfamily c, polypeptide 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17067568 1617888 Tubb1 tubulin, beta 1 class VI gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:11369202 1617888 Tubb1 tubulin, beta 1 class VI gene MP:0003405 abnormal platelet shape IAGP N RGD:5509061 20141003 MGI PMID:11369202 1617888 Tubb1 tubulin, beta 1 class VI gene MP:0003405 abnormal platelet shape IAGP N RGD:5509061 20141003 MGI PMID:15315966 1617888 Tubb1 tubulin, beta 1 class VI gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:15315966 1617888 Tubb1 tubulin, beta 1 class VI gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:11369202 1617893 Ccdc141 coiled-coil domain containing 141 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20180426 MGI PMID:27737934 1617893 Ccdc141 coiled-coil domain containing 141 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1617893 Ccdc141 coiled-coil domain containing 141 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20180426 MGI PMID:27737934 1617893 Ccdc141 coiled-coil domain containing 141 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20180426 MGI PMID:27737934 1617893 Ccdc141 coiled-coil domain containing 141 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20180426 MGI PMID:27737934 1617893 Ccdc141 coiled-coil domain containing 141 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20220421 MGI PMID:27737934 1617893 Ccdc141 coiled-coil domain containing 141 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20180426 MGI PMID:27737934 1617893 Ccdc141 coiled-coil domain containing 141 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20180426 MGI PMID:27737934 1617893 Ccdc141 coiled-coil domain containing 141 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20180426 MGI PMID:27737934 1617893 Ccdc141 coiled-coil domain containing 141 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:27737934 1617910 Mageb4 MAGE family member B4 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20230824 MGI PMID:37451217 1617911 Akirin2 akirin 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18066067 1617912 Ankrd13c ankyrin repeat domain 13c gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1617912 Ankrd13c ankyrin repeat domain 13c gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20220519 MGI 1617912 Ankrd13c ankyrin repeat domain 13c gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1617912 Ankrd13c ankyrin repeat domain 13c gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220519 MGI 1617912 Ankrd13c ankyrin repeat domain 13c gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1617919 Gm5547 predicted gene 5547 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0000106 abnormal basisphenoid bone morphology IEA N RGD:5509061 20170504 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0000562 polydactyly IEA N RGD:5509061 20170504 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0000914 exencephaly IEA N RGD:5509061 20170504 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0002989 small kidney IEA N RGD:5509061 20170504 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0004442 occipital bone foramen IEA N RGD:5509061 20170504 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0004463 basisphenoid bone foramen IEA N RGD:5509061 20170504 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0008182 decreased marginal zone B cell number IEA N RGD:5509061 20201231 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0012501 abnormal pericardial cavity morphology IEA N RGD:5509061 20170504 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0013830 abnormal intrathoracic topology of vagus nerve IEA N RGD:5509061 20170504 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0013985 abnormal umbilical vein topology IEA N RGD:5509061 20170504 MGI 1617922 Gm5544 predicted gene 5544 gene MP:0014018 embryo tumor IEA N RGD:5509061 20170504 MGI 1617925 Kprp keratinocyte expressed, proline-rich gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20200611 MGI PMID:30905808 1617925 Kprp keratinocyte expressed, proline-rich gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20200611 MGI PMID:30905808 1617925 Kprp keratinocyte expressed, proline-rich gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20200611 MGI PMID:30905808 1617925 Kprp keratinocyte expressed, proline-rich gene MP:0002497 increased IgE level IAGP N RGD:5509061 20200611 MGI PMID:30905808 1617925 Kprp keratinocyte expressed, proline-rich gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20200611 MGI PMID:30905808 1617925 Kprp keratinocyte expressed, proline-rich gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 1617925 Kprp keratinocyte expressed, proline-rich gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20240523 MGI 1617925 Kprp keratinocyte expressed, proline-rich gene MP:0009598 thin epidermis stratum granulosum IAGP N RGD:5509061 20200611 MGI PMID:30905808 1617925 Kprp keratinocyte expressed, proline-rich gene MP:0009605 decreased keratohyalin granule number IAGP N RGD:5509061 20200611 MGI PMID:30905808 1617925 Kprp keratinocyte expressed, proline-rich gene MP:0012572 increased susceptibility to chemically induced skin inflammation IAGP N RGD:5509061 20200611 MGI PMID:30905808 1617946 B3glct beta-3-glucosyltransferase gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0000111 cleft palate IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0000441 increased cranium width IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0000564 syndactyly IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0001265 decreased body size IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0002544 brachydactyly IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0002938 white spotting IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0004379 wide frontal bone IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0004380 short frontal bone IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0004472 broad nasal bone IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0010031 abnormal cranium size IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0010770 preweaning lethality IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0011861 increased cranium height IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0030066 short face IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0030099 facial asymmetry IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0030316 enlarged neurocranium IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0030384 short facial bone IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617946 B3glct beta-3-glucosyltransferase gene MP:0030420 short basicranium IAGP N RGD:5509061 20200514 MGI PMID:31600785 1617948 Kpna7 karyopherin subunit alpha 7 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20180125 MGI PMID:20699224 1617948 Kpna7 karyopherin subunit alpha 7 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20180125 MGI PMID:20699224 1617948 Kpna7 karyopherin subunit alpha 7 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20180125 MGI PMID:20699224 1617948 Kpna7 karyopherin subunit alpha 7 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20180125 MGI PMID:20699224 1617948 Kpna7 karyopherin subunit alpha 7 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180125 MGI PMID:20699224 1617948 Kpna7 karyopherin subunit alpha 7 gene MP:0020364 abnormal female germ cell physiology IAGP N RGD:5509061 20180125 MGI PMID:20699224 1617949 Nxpe5 neurexophilin and PC-esterase domain family, member 5 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20160804 MGI 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20191003 MGI PMID:31453335 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20191003 MGI PMID:31453335 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0001147 small testis IAGP N RGD:5509061 20191003 MGI PMID:31453335 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0001147 small testis IAGP N RGD:5509061 20211223 MGI PMID:32744506 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20191003 MGI PMID:31453335 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20191003 MGI PMID:31453335 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20211223 MGI PMID:32744506 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20191003 MGI PMID:31453335 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20211223 MGI PMID:32744506 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20220519 MGI 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20191003 MGI PMID:31453335 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20191003 MGI PMID:31453335 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20211223 MGI PMID:32744506 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20191003 MGI PMID:31453335 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20211223 MGI PMID:32744506 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20191003 MGI PMID:31453335 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20191003 MGI PMID:31453335 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20211223 MGI PMID:32744506 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0008967 absent chiasmata formation IAGP N RGD:5509061 20211223 MGI PMID:32744506 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20191003 MGI PMID:31453335 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20211223 MGI PMID:32744506 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20191003 MGI PMID:31453335 1617950 Zcwpw1 zinc finger, CW type with PWWP domain 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20211223 MGI PMID:32744506 1617951 Fbrsl1 fibrosin-like 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1617951 Fbrsl1 fibrosin-like 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 1617951 Fbrsl1 fibrosin-like 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1617951 Fbrsl1 fibrosin-like 1 gene MP:0000706 small thymus IEA N RGD:5509061 20220519 MGI 1617951 Fbrsl1 fibrosin-like 1 gene MP:0001147 small testis IEA N RGD:5509061 20220519 MGI 1617951 Fbrsl1 fibrosin-like 1 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20220519 MGI 1617951 Fbrsl1 fibrosin-like 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1617951 Fbrsl1 fibrosin-like 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20210128 MGI 1617951 Fbrsl1 fibrosin-like 1 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20220811 MGI 1617951 Fbrsl1 fibrosin-like 1 gene MP:0004930 small epididymis IEA N RGD:5509061 20220519 MGI 1617951 Fbrsl1 fibrosin-like 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1617951 Fbrsl1 fibrosin-like 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1617951 Fbrsl1 fibrosin-like 1 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20220519 MGI 1617952 Lrcol1 leucine rich colipase-like 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201022 MGI PMID:32588039 1617953 Pramel34 PRAME like 34 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38786026 1617954 Odaph odontogenesis associated phosphoprotein gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20211028 MGI PMID:33772937 1617954 Odaph odontogenesis associated phosphoprotein gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1617954 Odaph odontogenesis associated phosphoprotein gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1617954 Odaph odontogenesis associated phosphoprotein gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1617954 Odaph odontogenesis associated phosphoprotein gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1617954 Odaph odontogenesis associated phosphoprotein gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230601 MGI 1617954 Odaph odontogenesis associated phosphoprotein gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230601 MGI 1617954 Odaph odontogenesis associated phosphoprotein gene MP:0002648 delaminated enamel IAGP N RGD:5509061 20211028 MGI PMID:33772937 1617954 Odaph odontogenesis associated phosphoprotein gene MP:0002649 abnormal enamel rod pattern IAGP N RGD:5509061 20211028 MGI PMID:33772937 1617954 Odaph odontogenesis associated phosphoprotein gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20211028 MGI PMID:33772937 1617954 Odaph odontogenesis associated phosphoprotein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1617954 Odaph odontogenesis associated phosphoprotein gene MP:0003917 increased kidney weight IEA N RGD:5509061 20240523 MGI 1617954 Odaph odontogenesis associated phosphoprotein gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20211028 MGI PMID:33772937 1617956 Cep135 centrosomal protein 135 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220519 MGI 1617956 Cep135 centrosomal protein 135 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20200310 MGI 1617956 Cep135 centrosomal protein 135 gene MP:0000433 microcephaly IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0000562 polydactyly IEA N RGD:5509061 20210520 MGI 1617956 Cep135 centrosomal protein 135 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1617956 Cep135 centrosomal protein 135 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1617956 Cep135 centrosomal protein 135 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1617956 Cep135 centrosomal protein 135 gene MP:0001304 cataract IEA N RGD:5509061 20200310 MGI 1617956 Cep135 centrosomal protein 135 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1617956 Cep135 centrosomal protein 135 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 1617956 Cep135 centrosomal protein 135 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20230601 MGI 1617956 Cep135 centrosomal protein 135 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0008797 facial cleft IEA N RGD:5509061 20210520 MGI 1617956 Cep135 centrosomal protein 135 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0010995 abnormal lung alveolus development IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1617956 Cep135 centrosomal protein 135 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20210128 MGI 1617956 Cep135 centrosomal protein 135 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0020069 decreased neocortex size IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617956 Cep135 centrosomal protein 135 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20240718 MGI PMID:34237032 1617957 Gm1043 predicted gene 1043 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1617958 Nicol1 NELL2 interacting cell ontogeny regulator 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20230601 MGI PMID:37095084 1617958 Nicol1 NELL2 interacting cell ontogeny regulator 1 gene MP:0004935 epididymis degeneration IAGP N RGD:5509061 20230601 MGI PMID:37095084 1617958 Nicol1 NELL2 interacting cell ontogeny regulator 1 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20230601 MGI PMID:37095084 1617958 Nicol1 NELL2 interacting cell ontogeny regulator 1 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20230601 MGI PMID:37095084 1617958 Nicol1 NELL2 interacting cell ontogeny regulator 1 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20230601 MGI PMID:37095084 1617959 Rbm33 RNA binding motif protein 33 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1617961 Tbc1d2 TBC1 domain family, member 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20200310 MGI 1617961 Tbc1d2 TBC1 domain family, member 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20200310 MGI 1617962 Raet1e retinoic acid early transcript 1E gene MP:0003080 increased natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20160630 MGI PMID:25745066 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0001304 cataract IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0002764 short tibia IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0003718 maternal effect IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0005586 decreased tidal volume IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0010896 decreased lung compliance IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0011535 increased urination frequency IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0013673 increased mature NK cell number IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0020174 abnormal IgG level IAGP N RGD:5509061 20200310 MGI PMID:25111779 1617965 Zscan10 zinc finger and SCAN domain containing 10 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:25111779 1617967 Slc51b solute carrier family 51, beta subunit gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1617967 Slc51b solute carrier family 51, beta subunit gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1617967 Slc51b solute carrier family 51, beta subunit gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1617967 Slc51b solute carrier family 51, beta subunit gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 1617967 Slc51b solute carrier family 51, beta subunit gene MP:0003960 increased lean body mass IEA N RGD:5509061 20190502 MGI 1617967 Slc51b solute carrier family 51, beta subunit gene MP:0009709 hydrometra IEA N RGD:5509061 20210128 MGI 1617967 Slc51b solute carrier family 51, beta subunit gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20190502 MGI 1617967 Slc51b solute carrier family 51, beta subunit gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1617970 Dixdc1 DIX domain containing 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1617970 Dixdc1 DIX domain containing 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20160721 MGI PMID:22832659 1617970 Dixdc1 DIX domain containing 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160721 MGI PMID:22832659 1617970 Dixdc1 DIX domain containing 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160721 MGI PMID:22832659 1617970 Dixdc1 DIX domain containing 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20160721 MGI PMID:22832659 1617970 Dixdc1 DIX domain containing 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20160721 MGI PMID:22832659 1617970 Dixdc1 DIX domain containing 1 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20220519 MGI 1617971 Pate2 prostate and testis expressed 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1617971 Pate2 prostate and testis expressed 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1617973 E130311K13Rik RIKEN cDNA E130311K13 gene gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1617973 E130311K13Rik RIKEN cDNA E130311K13 gene gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1617975 Fat4 FAT atypical cadherin 4 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0004017 duplex kidney IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617975 Fat4 FAT atypical cadherin 4 gene MP:0011493 double ureter IAGP N RGD:5509061 20141003 MGI PMID:18604206 1617975 Fat4 FAT atypical cadherin 4 gene MP:0012279 wide sternum IAGP N RGD:5509061 20141003 MGI PMID:21303848 1617977 Rft1 RFT1 homolog gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 1617977 Rft1 RFT1 homolog gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1617977 Rft1 RFT1 homolog gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20210128 MGI 1617977 Rft1 RFT1 homolog gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1617977 Rft1 RFT1 homolog gene MP:0004357 long tibia IEA N RGD:5509061 20221215 MGI 1617977 Rft1 RFT1 homolog gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1617977 Rft1 RFT1 homolog gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1617977 Rft1 RFT1 homolog gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 1617977 Rft1 RFT1 homolog gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1617977 Rft1 RFT1 homolog gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1617977 Rft1 RFT1 homolog gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:26522984 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20200310 MGI PMID:26522984 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0003717 pallor IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:26522984 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:26522984 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20200310 MGI PMID:26522984 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0012732 abnormal perineural vascular plexus morphology IAGP N RGD:5509061 20200310 MGI PMID:17967885 1617978 Zmiz1 zinc finger, MIZ-type containing 1 gene MP:0014224 increased ileal goblet cell number IAGP N RGD:5509061 20200310 MGI PMID:26522984 1617982 Phf8 PHD finger protein 8 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20211021 MGI 1617982 Phf8 PHD finger protein 8 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230601 MGI 1617982 Phf8 PHD finger protein 8 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20191114 MGI PMID:28485378 1617982 Phf8 PHD finger protein 8 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20191114 MGI PMID:28485378 1617982 Phf8 PHD finger protein 8 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20191128 MGI PMID:29317619 1617982 Phf8 PHD finger protein 8 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1617982 Phf8 PHD finger protein 8 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210520 MGI 1617982 Phf8 PHD finger protein 8 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1617982 Phf8 PHD finger protein 8 gene MP:0003063 increased coping response IAGP N RGD:5509061 20191114 MGI PMID:28485378 1617982 Phf8 PHD finger protein 8 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20191128 MGI PMID:29317619 1617982 Phf8 PHD finger protein 8 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20230601 MGI 1617982 Phf8 PHD finger protein 8 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20191128 MGI PMID:29317619 1617982 Phf8 PHD finger protein 8 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20191114 MGI PMID:28485378 1617982 Phf8 PHD finger protein 8 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20230601 MGI 1617982 Phf8 PHD finger protein 8 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1617982 Phf8 PHD finger protein 8 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20230601 MGI 1617982 Phf8 PHD finger protein 8 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 1617982 Phf8 PHD finger protein 8 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20191128 MGI PMID:29317619 1617982 Phf8 PHD finger protein 8 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20191128 MGI PMID:29317619 1617982 Phf8 PHD finger protein 8 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20230601 MGI 1617982 Phf8 PHD finger protein 8 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20191128 MGI PMID:29317619 1617982 Phf8 PHD finger protein 8 gene MP:0020870 decreased thigmotaxis IAGP N RGD:5509061 20191114 MGI PMID:28485378 1617982 Phf8 PHD finger protein 8 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:29317619 1617983 Tmem88b transmembrane protein 88B gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1617983 Tmem88b transmembrane protein 88B gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1617983 Tmem88b transmembrane protein 88B gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1617983 Tmem88b transmembrane protein 88B gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1617985 Atp8b5 ATPase, class I, type 8B, member 5 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38697008 1617987 Islr2 immunoglobulin superfamily containing leucine-rich repeat 2 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:24930700 1617987 Islr2 immunoglobulin superfamily containing leucine-rich repeat 2 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19755105 1617987 Islr2 immunoglobulin superfamily containing leucine-rich repeat 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:19755105 1617987 Islr2 immunoglobulin superfamily containing leucine-rich repeat 2 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:19755105 1617987 Islr2 immunoglobulin superfamily containing leucine-rich repeat 2 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19755105 1617987 Islr2 immunoglobulin superfamily containing leucine-rich repeat 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24930700 1617987 Islr2 immunoglobulin superfamily containing leucine-rich repeat 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:24930700 1617987 Islr2 immunoglobulin superfamily containing leucine-rich repeat 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19755105 1617987 Islr2 immunoglobulin superfamily containing leucine-rich repeat 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19755105 1617987 Islr2 immunoglobulin superfamily containing leucine-rich repeat 2 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:24930700 1617987 Islr2 immunoglobulin superfamily containing leucine-rich repeat 2 gene MP:0008129 absent brain internal capsule IAGP N RGD:5509061 20141003 MGI PMID:24930700 1617987 Islr2 immunoglobulin superfamily containing leucine-rich repeat 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:19755105 1617987 Islr2 immunoglobulin superfamily containing leucine-rich repeat 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:19755105 1617987 Islr2 immunoglobulin superfamily containing leucine-rich repeat 2 gene MP:0009970 increased hippocampus pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:24930700 1617987 Islr2 immunoglobulin superfamily containing leucine-rich repeat 2 gene MP:0012484 decreased corticospinal tract size IAGP N RGD:5509061 20141003 MGI PMID:24930700 1617988 Dennd5b DENN domain containing 5B gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20221215 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220519 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20220519 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20220519 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20221215 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0003896 prolonged PR interval IEA N RGD:5509061 20220519 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20220519 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20220519 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210520 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210826 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220519 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0009485 distended ileum IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20221215 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20221215 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20221215 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0010360 decreased liver free fatty acids level IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210826 MGI 1617988 Dennd5b DENN domain containing 5B gene MP:0011503 distended jejunum IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0011881 distended duodenum IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0013957 increased small intestine length IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0020182 abnormal body mass index IAGP N RGD:5509061 20190725 MGI PMID:30837651 1617988 Dennd5b DENN domain containing 5B gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210520 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210520 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210128 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0000747 muscle weakness IAGP N RGD:5509061 20170209 MGI PMID:26035871 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20210520 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0001258 decreased body length IEA N RGD:5509061 20210520 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170209 MGI PMID:26035871 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0001265 decreased body size IAGP N RGD:5509061 20160128 MGI PMID:25774500 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20201022 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20190502 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160128 MGI PMID:25774500 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170209 MGI PMID:26035871 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20221215 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0002608 increased hematocrit IEA N RGD:5509061 20210128 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20170209 MGI PMID:26035871 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210520 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20170209 MGI PMID:26035871 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20160128 MGI PMID:25774500 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20170209 MGI PMID:26035871 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20160128 MGI PMID:25774500 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20170209 MGI PMID:26035871 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160128 MGI PMID:25774500 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0005150 cachexia IAGP N RGD:5509061 20160128 MGI PMID:25774500 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0009084 blind uterus IEA N RGD:5509061 20210826 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20190502 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20160128 MGI PMID:25774500 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20160128 MGI PMID:25774500 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20170209 MGI PMID:26035871 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210520 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20170209 MGI PMID:26035871 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0010240 decreased skeletal muscle size IAGP N RGD:5509061 20160128 MGI PMID:25774500 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20160128 MGI PMID:25774500 1617991 Lmod3 leiomodin 3 (fetal) gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210520 MGI 1617993 Gpr141b G protein-coupled receptor 141B gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1617995 Shfl shiftless antiviral inhibitor of ribosomal frameshifting gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20200402 MGI 1617995 Shfl shiftless antiviral inhibitor of ribosomal frameshifting gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20200402 MGI 1617995 Shfl shiftless antiviral inhibitor of ribosomal frameshifting gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20231207 MGI 1618005 Nol4 nucleolar protein 4 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210826 MGI 1618005 Nol4 nucleolar protein 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1618005 Nol4 nucleolar protein 4 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210826 MGI 1618005 Nol4 nucleolar protein 4 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210520 MGI 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618006 Gpr82 G protein-coupled receptor 82 gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20210401 MGI PMID:22216272 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0000618 small salivary gland IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0000653 abnormal sex gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:21149719 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001140 abnormal vagina epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001142 abnormal vagina orifice morphology IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:21516099 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:21149719 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:21516099 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:21149719 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:21516099 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0002016 ovary cyst IAGP N RGD:5509061 20220407 MGI PMID:21149719 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0002163 abnormal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0002716 small male preputial gland IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0002717 abnormal male preputial gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:21149719 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0003379 absent sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0003531 abnormal vagina development IAGP N RGD:5509061 20141003 MGI PMID:21516099 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0003572 abnormal uterus development IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:21516099 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0005148 seminal vesicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0005183 abnormal circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0005188 small penis IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0008297 retention of the adrenal gland x-zone IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21516099 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0008994 early vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:21149719 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:17595229 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:21149719 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:21516099 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20141003 MGI PMID:21516099 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20141003 MGI PMID:21149719 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0013317 abnormal seminal vesicle development IAGP N RGD:5509061 20141204 MGI PMID:17563351 1618007 Kiss1 KiSS-1 metastasis-suppressor gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:17563351 1618008 Tmem255b transmembrane protein 255B gene MP:0000745 tremors IEA N RGD:5509061 20141003 MGI 1618008 Tmem255b transmembrane protein 255B gene MP:0002833 increased heart weight IEA N RGD:5509061 20160804 MGI 1618011 Ssc5d scavenger receptor cysteine rich family, 5 domains gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1618013 Zfp384 zinc finger protein 384 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:15189450 1618013 Zfp384 zinc finger protein 384 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15189450 1618013 Zfp384 zinc finger protein 384 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15189450 1618013 Zfp384 zinc finger protein 384 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15189450 1618013 Zfp384 zinc finger protein 384 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15189450 1618016 Greb1 gene regulated by estrogen in breast cancer protein gene MP:0001258 decreased body length IEA N RGD:5509061 20190502 MGI 1618016 Greb1 gene regulated by estrogen in breast cancer protein gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20240418 MGI PMID:38431630 1618016 Greb1 gene regulated by estrogen in breast cancer protein gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20240418 MGI PMID:38431630 1618016 Greb1 gene regulated by estrogen in breast cancer protein gene MP:0001935 decreased litter size IAGP N RGD:5509061 20240418 MGI PMID:38431630 1618016 Greb1 gene regulated by estrogen in breast cancer protein gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20240418 MGI PMID:38431630 1618016 Greb1 gene regulated by estrogen in breast cancer protein gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20240418 MGI PMID:38431630 1618016 Greb1 gene regulated by estrogen in breast cancer protein gene MP:0009662 abnormal uterine receptivity IAGP N RGD:5509061 20240418 MGI PMID:38431630 1618016 Greb1 gene regulated by estrogen in breast cancer protein gene MP:0009663 abnormal uterine-embryonic axis IAGP N RGD:5509061 20240418 MGI PMID:38431630 1618016 Greb1 gene regulated by estrogen in breast cancer protein gene MP:0009664 abnormal luminal closure IAGP N RGD:5509061 20240418 MGI PMID:38431630 1618016 Greb1 gene regulated by estrogen in breast cancer protein gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20240418 MGI PMID:38431630 1618016 Greb1 gene regulated by estrogen in breast cancer protein gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1618017 Mgat5b mannoside acetylglucosaminyltransferase 5, isoenzyme B gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:23761899 1618017 Mgat5b mannoside acetylglucosaminyltransferase 5, isoenzyme B gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20150226 MGI PMID:23118208 1618017 Mgat5b mannoside acetylglucosaminyltransferase 5, isoenzyme B gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22715095 1618017 Mgat5b mannoside acetylglucosaminyltransferase 5, isoenzyme B gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:23761899 1618017 Mgat5b mannoside acetylglucosaminyltransferase 5, isoenzyme B gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20150226 MGI PMID:23118208 1618017 Mgat5b mannoside acetylglucosaminyltransferase 5, isoenzyme B gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23761899 1618017 Mgat5b mannoside acetylglucosaminyltransferase 5, isoenzyme B gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:23761899 1618017 Mgat5b mannoside acetylglucosaminyltransferase 5, isoenzyme B gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1618017 Mgat5b mannoside acetylglucosaminyltransferase 5, isoenzyme B gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1618017 Mgat5b mannoside acetylglucosaminyltransferase 5, isoenzyme B gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1618017 Mgat5b mannoside acetylglucosaminyltransferase 5, isoenzyme B gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20150226 MGI PMID:23118208 1618017 Mgat5b mannoside acetylglucosaminyltransferase 5, isoenzyme B gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:23761899 1618017 Mgat5b mannoside acetylglucosaminyltransferase 5, isoenzyme B gene MP:0020155 enhanced humoral immune response IAGP N RGD:5509061 20150226 MGI PMID:23118208 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0008556 abnormal tumor necrosis factor secretion IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618104 Tarm1 T cell-interacting, activating receptor on myeloid cells 1 gene MP:0008704 abnormal interleukin-6 secretion IAGP N RGD:5509061 20210325 MGI PMID:33397982 1618107 Ggn gametogenetin gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:23451117 1618107 Ggn gametogenetin gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23451117 1618110 Meiosin meiosis initiator gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20210107 MGI PMID:32032549 1618110 Meiosin meiosis initiator gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20210107 MGI PMID:32032549 1618110 Meiosin meiosis initiator gene MP:0005159 azoospermia IAGP N RGD:5509061 20210107 MGI PMID:32032549 1618110 Meiosin meiosis initiator gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20210107 MGI PMID:32032549 1618110 Meiosin meiosis initiator gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20210107 MGI PMID:32032549 1618110 Meiosin meiosis initiator gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20210107 MGI PMID:32032549 1618110 Meiosin meiosis initiator gene MP:0008967 absent chiasmata formation IAGP N RGD:5509061 20210107 MGI PMID:32032549 1618110 Meiosin meiosis initiator gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20210107 MGI PMID:32032549 1618110 Meiosin meiosis initiator gene MP:0009564 abnormal meiotic configurations IAGP N RGD:5509061 20210107 MGI PMID:32032549 1618110 Meiosin meiosis initiator gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20210107 MGI PMID:32032549 1618110 Meiosin meiosis initiator gene MP:0013236 ovary degeneration IAGP N RGD:5509061 20210107 MGI PMID:32032549 1618110 Meiosin meiosis initiator gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20210107 MGI PMID:32032549 1618112 Psg22 pregnancy-specific beta-1-glycoprotein 22 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210520 MGI 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0001297 microphthalmia IEA N RGD:5509061 20240523 MGI 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0001787 pericardial edema IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0001914 hemorrhage IEA N RGD:5509061 20240523 MGI 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0002083 premature death IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20231207 MGI 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0002188 small heart IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20231207 MGI 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0005385 cardiovascular system phenotype IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0006111 abnormal coronary circulation IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0010768 mortality/aging IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36745292 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1618114 Bicra BRD4 interacting chromatin remodeling complex associated protein gene MP:0031634 decreased heart right ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:36745292 1618115 Garin5b golgi associated RAB2 interactor family member 5B gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20240801 MGI PMID:38935810 1618115 Garin5b golgi associated RAB2 interactor family member 5B gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240801 MGI PMID:38935810 1618115 Garin5b golgi associated RAB2 interactor family member 5B gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240801 MGI PMID:38935810 1618115 Garin5b golgi associated RAB2 interactor family member 5B gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20240801 MGI PMID:38935810 1618116 Gp6 glycoprotein 6 platelet gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20151119 MGI PMID:23448972 1618116 Gp6 glycoprotein 6 platelet gene MP:0001935 decreased litter size IAGP N RGD:5509061 20151119 MGI PMID:23448972 1618116 Gp6 glycoprotein 6 platelet gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20170105 MGI 1618116 Gp6 glycoprotein 6 platelet gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12738669 1618116 Gp6 glycoprotein 6 platelet gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:12738669 1618116 Gp6 glycoprotein 6 platelet gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20151119 MGI PMID:23448972 1618116 Gp6 glycoprotein 6 platelet gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23112346 1618116 Gp6 glycoprotein 6 platelet gene MP:0004357 long tibia IEA N RGD:5509061 20201022 MGI 1618116 Gp6 glycoprotein 6 platelet gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1618116 Gp6 glycoprotein 6 platelet gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20170105 MGI 1618116 Gp6 glycoprotein 6 platelet gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20151119 MGI PMID:23448972 1618116 Gp6 glycoprotein 6 platelet gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20201001 MGI PMID:12738669 1618116 Gp6 glycoprotein 6 platelet gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20201001 MGI PMID:12738669 1618116 Gp6 glycoprotein 6 platelet gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141016 MGI PMID:24368846 1618116 Gp6 glycoprotein 6 platelet gene MP:0011898 abnormal platelet cell number IAGP N RGD:5509061 20151119 MGI PMID:23448972 1618116 Gp6 glycoprotein 6 platelet gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20210128 MGI 1618118 Atg4c autophagy related 4C, cysteine peptidase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:17442669 1618118 Atg4c autophagy related 4C, cysteine peptidase gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20200310 MGI PMID:17442669 1618118 Atg4c autophagy related 4C, cysteine peptidase gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200310 MGI PMID:17442669 1618119 Kank4 KN motif and ankyrin repeat domains 4 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20241107 MGI PMID:35477278 1618119 Kank4 KN motif and ankyrin repeat domains 4 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20241107 MGI PMID:35477278 1618119 Kank4 KN motif and ankyrin repeat domains 4 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20241107 MGI PMID:35477278 1618119 Kank4 KN motif and ankyrin repeat domains 4 gene MP:0012201 decreased endothelial cell proliferation IAGP N RGD:5509061 20241107 MGI PMID:35477278 1618124 Ppp1r26 protein phosphatase 1, regulatory subunit 26 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1618124 Ppp1r26 protein phosphatase 1, regulatory subunit 26 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20230601 MGI 1618130 Spata31d1c spermatogenesis associated 31 subfamily D, member 1C gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1618131 Cntnap3 contactin associated protein-like 3 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20180913 MGI PMID:26807827 1618134 C2cd4c C2 calcium-dependent domain containing 4C gene MP:0001262 decreased body weight IAGP N RGD:5509061 20171214 MGI PMID:27349930 1618134 C2cd4c C2 calcium-dependent domain containing 4C gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20240523 MGI 1618134 C2cd4c C2 calcium-dependent domain containing 4C gene MP:0011940 decreased food intake IEA N RGD:5509061 20240523 MGI 1618135 Npffr1 neuropeptide FF receptor 1 gene MP:0001746 abnormal pituitary secretion IAGP N RGD:5509061 20150827 MGI PMID:24823392 1618135 Npffr1 neuropeptide FF receptor 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20150827 MGI PMID:24823392 1618135 Npffr1 neuropeptide FF receptor 1 gene MP:0001934 increased litter size IAGP N RGD:5509061 20150827 MGI PMID:24823392 1618135 Npffr1 neuropeptide FF receptor 1 gene MP:0005131 increased follicle stimulating hormone level IAGP N RGD:5509061 20150827 MGI PMID:24823392 1618135 Npffr1 neuropeptide FF receptor 1 gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20150827 MGI PMID:24823392 1618135 Npffr1 neuropeptide FF receptor 1 gene MP:0005133 increased luteinizing hormone level IAGP N RGD:5509061 20150827 MGI PMID:24823392 1618135 Npffr1 neuropeptide FF receptor 1 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20150827 MGI PMID:24823392 1618135 Npffr1 neuropeptide FF receptor 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20150827 MGI PMID:24823392 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0001194 dermatitis IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0001925 male infertility IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0004971 dermal hyperplasia IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20210429 MGI PMID:29649548 1618137 Adamts14 ADAM metallopeptidase with thrombospondin type 1 motif 14 gene MP:0031395 cutaneous mastocytosis IAGP N RGD:5509061 20220721 MGI PMID:29649548 1618138 Il20ra interleukin 20 receptor, alpha gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:21844205 1618138 Il20ra interleukin 20 receptor, alpha gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:24211183 1618138 Il20ra interleukin 20 receptor, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24211183 1618138 Il20ra interleukin 20 receptor, alpha gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1618138 Il20ra interleukin 20 receptor, alpha gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:21844205 1618138 Il20ra interleukin 20 receptor, alpha gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:24211183 1618138 Il20ra interleukin 20 receptor, alpha gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:21844205 1618138 Il20ra interleukin 20 receptor, alpha gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1618138 Il20ra interleukin 20 receptor, alpha gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21844205 1618138 Il20ra interleukin 20 receptor, alpha gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:21844205 1618138 Il20ra interleukin 20 receptor, alpha gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1618138 Il20ra interleukin 20 receptor, alpha gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:21844205 1618139 Gm4922 predicted gene 4922 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 1618139 Gm4922 predicted gene 4922 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1618139 Gm4922 predicted gene 4922 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20181227 MGI 1618139 Gm4922 predicted gene 4922 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20190502 MGI 1618141 Slc38a8 solute carrier family 38, member 8 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1618141 Slc38a8 solute carrier family 38, member 8 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20240118 MGI PMID:37862028 1618141 Slc38a8 solute carrier family 38, member 8 gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20231109 MGI PMID:36735752 1618141 Slc38a8 solute carrier family 38, member 8 gene MP:0004165 abnormal lateral geniculate nucleus morphology IAGP N RGD:5509061 20240118 MGI PMID:37862028 1618141 Slc38a8 solute carrier family 38, member 8 gene MP:0005100 abnormal choroid pigmentation IAGP N RGD:5509061 20240118 MGI PMID:37862028 1618141 Slc38a8 solute carrier family 38, member 8 gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20240118 MGI PMID:37862028 1618141 Slc38a8 solute carrier family 38, member 8 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20240118 MGI PMID:37862028 1618141 Slc38a8 solute carrier family 38, member 8 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20231109 MGI PMID:36735752 1618141 Slc38a8 solute carrier family 38, member 8 gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20240118 MGI PMID:37862028 1618141 Slc38a8 solute carrier family 38, member 8 gene MP:0009790 decreased susceptibility to viral infection induced morbidity/mortality IAGP N RGD:5509061 20231109 MGI PMID:36735752 1618141 Slc38a8 solute carrier family 38, member 8 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20240118 MGI PMID:37862028 1618141 Slc38a8 solute carrier family 38, member 8 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20240118 MGI PMID:37862028 1618141 Slc38a8 solute carrier family 38, member 8 gene MP:0030743 decreased aspartic acid level IAGP N RGD:5509061 20231109 MGI PMID:36735752 1618142 Rfwd3 ring finger and WD repeat domain 3 gene MP:0001127 small ovary IAGP N RGD:5509061 20200310 MGI PMID:28691929 1618142 Rfwd3 ring finger and WD repeat domain 3 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220407 MGI PMID:28691929 1618142 Rfwd3 ring finger and WD repeat domain 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:28691929 1618142 Rfwd3 ring finger and WD repeat domain 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:28691929 1618142 Rfwd3 ring finger and WD repeat domain 3 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:28691929 1618142 Rfwd3 ring finger and WD repeat domain 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:28691929 1618142 Rfwd3 ring finger and WD repeat domain 3 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20200310 MGI PMID:28691929 1618142 Rfwd3 ring finger and WD repeat domain 3 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20200310 MGI PMID:28691929 1618142 Rfwd3 ring finger and WD repeat domain 3 gene MP:0014040 increased cellular sensitivity to DNA damaging agents IAGP N RGD:5509061 20200310 MGI PMID:28691929 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0000525 renal tubular acidosis IAGP N RGD:5509061 20141003 MGI PMID:22082831 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20240208 MGI PMID:22082831 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20220317 MGI PMID:35216333 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20220317 MGI PMID:35216333 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:22082831 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:22082831 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20220317 MGI PMID:35216333 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:22082831 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0003017 decreased circulating bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:22082831 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0003099 retina detachment IAGP N RGD:5509061 20220317 MGI PMID:35216333 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0003353 decreased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:22082831 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20220317 MGI PMID:35216333 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0005522 increased circulating atrial natriuretic factor IAGP N RGD:5509061 20141003 MGI PMID:22082831 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0005527 increased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:22082831 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:22082831 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22082831 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22082831 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20220317 MGI PMID:35216333 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20220317 MGI PMID:35216333 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22082831 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22082831 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0011462 increased urine bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:22082831 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20220317 MGI PMID:35216333 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20220317 MGI PMID:35216333 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20220317 MGI PMID:35216333 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0012671 retina spots IAGP N RGD:5509061 20220317 MGI PMID:35216333 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0020962 increased c-wave amplitude IAGP N RGD:5509061 20220317 MGI PMID:35216333 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0020977 decreased FO-wave amplitude IAGP N RGD:5509061 20220317 MGI PMID:35216333 1618147 Slc4a5 solute carrier family 4, sodium bicarbonate cotransporter, member 5 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:35216333 1618148 Eva1a eva-1 homolog A, regulator of programmed cell death gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20210415 MGI PMID:26905199 1618148 Eva1a eva-1 homolog A, regulator of programmed cell death gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20211021 MGI 1618148 Eva1a eva-1 homolog A, regulator of programmed cell death gene MP:0012204 abnormal neuronal stem cell physiology IAGP N RGD:5509061 20210415 MGI PMID:26905199 1618148 Eva1a eva-1 homolog A, regulator of programmed cell death gene MP:0012207 decreased neuronal stem cell self-renewal IAGP N RGD:5509061 20210415 MGI PMID:26905199 1618148 Eva1a eva-1 homolog A, regulator of programmed cell death gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20210415 MGI PMID:26905199 1618151 Crocc ciliary rootlet coiled-coil, rootletin gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1618151 Crocc ciliary rootlet coiled-coil, rootletin gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:15870283 1618151 Crocc ciliary rootlet coiled-coil, rootletin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:15870283 1618152 Sh2d5 SH2 domain containing 5 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20201231 MGI 1618152 Sh2d5 SH2 domain containing 5 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20200310 MGI 1618153 Asap3 ArfGAP with SH3 domain, ankyrin repeat and PH domain 3 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1618153 Asap3 ArfGAP with SH3 domain, ankyrin repeat and PH domain 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20151210 MGI PMID:24360809 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:14608380 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:14608380 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20141003 MGI 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:14608380 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:20152175 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:14608380 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20152175 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20654612 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:42071 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:7119666 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000919 cranioschisis IAGP N RGD:5509061 20141003 MGI PMID:20654612 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000929 open neural tube IEA N RGD:5509061 20111116 MGI 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:17566405 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:21245842 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001192 scaly skin IAGP N RGD:5509061 20220630 MGI PMID:35440748 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001200 thick skin IAGP N RGD:5509061 20220630 MGI PMID:35440748 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:21245842 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:22094257 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20170518 MGI PMID:26975724 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21245842 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22094257 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20141003 MGI 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:21245842 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20152175 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14608380 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:20152175 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:1782873 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0001890 anencephaly IEA N RGD:5509061 20111116 MGI 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22094257 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:22094257 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:22094257 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17566405 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20220630 MGI PMID:35440748 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20141003 MGI 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20152175 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20654612 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22094257 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17566405 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002492 decreased IgE level IEA N RGD:5509061 20160804 MGI 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:1782873 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20170518 MGI PMID:26975724 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:14608380 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:20654612 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:21262862 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:7119666 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:7613032 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:8275849 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:8575765 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:14608380 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:20152175 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:20654612 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:21245842 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:7119666 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:8275849 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003313 abnormal locomotor activation IEA N RGD:5509061 20141003 MGI 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:1615432 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:20152175 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:42072 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:8275849 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20151210 MGI PMID:24360809 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7119666 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22094257 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20141003 MGI PMID:14608380 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0004603 absent vertebral arch IAGP N RGD:5509061 20141003 MGI PMID:14608380 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0004604 abnormal vertebral pedicle morphology IAGP N RGD:5509061 20240404 MGI PMID:20654612 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:22094257 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20160804 MGI 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20160804 MGI 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:20654612 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20220630 MGI PMID:35440748 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:17566405 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0009474 thick epidermis stratum spinosum IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22094257 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20170518 MGI PMID:26975724 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20151210 MGI PMID:24360809 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22094257 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0009929 meningomyelocele IAGP N RGD:5509061 20141003 MGI PMID:17566405 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170518 MGI PMID:26975724 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20151210 MGI PMID:24360809 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21245842 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20152175 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14608380 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20151210 MGI PMID:24360809 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20654612 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0012547 spina bifida cystica IAGP N RGD:5509061 20141003 MGI PMID:14608380 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0013531 abnormal periderm development IAGP N RGD:5509061 20151210 MGI PMID:24360809 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0030605 abnormal corneocyte morphology IAGP N RGD:5509061 20180628 MGI PMID:16949565 1618154 Grhl3 grainyhead like transcription factor 3 gene MP:0031154 intestinal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:16949565 1618155 Ncmap noncompact myelin associated protein gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240627 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20201022 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200310 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0000274 enlarged heart IEA N RGD:5509061 20200310 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20220811 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210128 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200310 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200310 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0001200 thick skin IEA N RGD:5509061 20210128 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201022 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20200310 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20201022 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20200310 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0009709 hydrometra IEA N RGD:5509061 20200310 MGI 1618156 Pdik1l PDLIM1 interacting kinase 1 like gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1618157 Ciart circadian associated repressor of transcription gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20150226 MGI PMID:24736997 1618157 Ciart circadian associated repressor of transcription gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24385426 1618157 Ciart circadian associated repressor of transcription gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:24736997 1618157 Ciart circadian associated repressor of transcription gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:24737000 1618158 Gm128 predicted gene 128 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1618158 Gm128 predicted gene 128 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:22621904 1618165 Eif5b eukaryotic translation initiation factor 5B gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240919 MGI 1618165 Eif5b eukaryotic translation initiation factor 5B gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241017 MGI 1618165 Eif5b eukaryotic translation initiation factor 5B gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220519 MGI 1618165 Eif5b eukaryotic translation initiation factor 5B gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241017 MGI 1618165 Eif5b eukaryotic translation initiation factor 5B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1618165 Eif5b eukaryotic translation initiation factor 5B gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20240919 MGI 1618169 Cplx4 complexin 4 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20200310 MGI PMID:19386896 1618169 Cplx4 complexin 4 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20200310 MGI PMID:19386896 1618169 Cplx4 complexin 4 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230119 MGI 1618169 Cplx4 complexin 4 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:19386896 1618169 Cplx4 complexin 4 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:19386896 1618169 Cplx4 complexin 4 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 1618169 Cplx4 complexin 4 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20230119 MGI 1618169 Cplx4 complexin 4 gene MP:0008520 disorganized retina outer plexiform layer IAGP N RGD:5509061 20200310 MGI PMID:19386896 1618172 Fam167a family with sequence similarity 167, member A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1618172 Fam167a family with sequence similarity 167, member A gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1618172 Fam167a family with sequence similarity 167, member A gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20230601 MGI 1618172 Fam167a family with sequence similarity 167, member A gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 1618172 Fam167a family with sequence similarity 167, member A gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1618172 Fam167a family with sequence similarity 167, member A gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1618172 Fam167a family with sequence similarity 167, member A gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1618172 Fam167a family with sequence similarity 167, member A gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1618172 Fam167a family with sequence similarity 167, member A gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1618172 Fam167a family with sequence similarity 167, member A gene MP:0001148 enlarged testis IEA N RGD:5509061 20230601 MGI 1618172 Fam167a family with sequence similarity 167, member A gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20230601 MGI 1618172 Fam167a family with sequence similarity 167, member A gene MP:0010935 increased airway resistance IEA N RGD:5509061 20230601 MGI 1618172 Fam167a family with sequence similarity 167, member A gene MP:0011047 increased lung tissue damping IEA N RGD:5509061 20230601 MGI 1618173 Shisa2 shisa family member 2 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:17481602 1618173 Shisa2 shisa family member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17481602 1618173 Shisa2 shisa family member 2 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:17481602 1618173 Shisa2 shisa family member 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17481602 1618175 Pacs2 phosphofurin acidic cluster sorting protein 2 gene MP:0002764 short tibia IEA N RGD:5509061 20200310 MGI 1618175 Pacs2 phosphofurin acidic cluster sorting protein 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20200310 MGI PMID:18296443 1618175 Pacs2 phosphofurin acidic cluster sorting protein 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20200310 MGI 1618175 Pacs2 phosphofurin acidic cluster sorting protein 2 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:18296443 1618175 Pacs2 phosphofurin acidic cluster sorting protein 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200310 MGI 1618176 Cep170b centrosomal protein 170B gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230119 MGI 1618176 Cep170b centrosomal protein 170B gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230601 MGI 1618177 Nrde2 nrde-2 necessary for RNA interference, domain containing gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1618177 Nrde2 nrde-2 necessary for RNA interference, domain containing gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1618177 Nrde2 nrde-2 necessary for RNA interference, domain containing gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1618178 Ccdc157 coiled-coil domain containing 157 gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20240404 MGI PMID:38509755 1618178 Ccdc157 coiled-coil domain containing 157 gene MP:0001925 male infertility IAGP N RGD:5509061 20240404 MGI PMID:38509755 1618178 Ccdc157 coiled-coil domain containing 157 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240404 MGI PMID:38509755 1618178 Ccdc157 coiled-coil domain containing 157 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240404 MGI PMID:38509755 1618178 Ccdc157 coiled-coil domain containing 157 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20240404 MGI PMID:38509755 1618178 Ccdc157 coiled-coil domain containing 157 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20240404 MGI PMID:38509755 1618178 Ccdc157 coiled-coil domain containing 157 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20240404 MGI PMID:38509755 1618178 Ccdc157 coiled-coil domain containing 157 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20240404 MGI PMID:38509755 1618178 Ccdc157 coiled-coil domain containing 157 gene MP:0008975 delayed male fertility IAGP N RGD:5509061 20240404 MGI PMID:38509755 1618178 Ccdc157 coiled-coil domain containing 157 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240404 MGI PMID:38509755 1618178 Ccdc157 coiled-coil domain containing 157 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20240404 MGI PMID:38509755 1618178 Ccdc157 coiled-coil domain containing 157 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20240404 MGI PMID:38509755 1618178 Ccdc157 coiled-coil domain containing 157 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20240404 MGI PMID:38509755 1618178 Ccdc157 coiled-coil domain containing 157 gene MP:0030980 abnormal acroplaxome morphology IAGP N RGD:5509061 20240404 MGI PMID:38509755 1618178 Ccdc157 coiled-coil domain containing 157 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20240404 MGI PMID:38509755 1618179 Traf3ip3 TRAF3 interacting protein 3 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20200310 MGI 1618179 Traf3ip3 TRAF3 interacting protein 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:26195727 1618179 Traf3ip3 TRAF3 interacting protein 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:26195727 1618179 Traf3ip3 TRAF3 interacting protein 3 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20200310 MGI PMID:26195727 1618179 Traf3ip3 TRAF3 interacting protein 3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:26195727 1618179 Traf3ip3 TRAF3 interacting protein 3 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:26195727 1618179 Traf3ip3 TRAF3 interacting protein 3 gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20200310 MGI PMID:26195727 1618179 Traf3ip3 TRAF3 interacting protein 3 gene MP:0010836 decreased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20200310 MGI PMID:26195727 1618179 Traf3ip3 TRAF3 interacting protein 3 gene MP:0010839 decreased CD8-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20200310 MGI PMID:26195727 1618182 Tnrc6b trinucleotide repeat containing 6b gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20221215 MGI 1618182 Tnrc6b trinucleotide repeat containing 6b gene MP:0001258 decreased body length IEA N RGD:5509061 20221215 MGI 1618182 Tnrc6b trinucleotide repeat containing 6b gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180315 MGI PMID:28811219 1618182 Tnrc6b trinucleotide repeat containing 6b gene MP:0001924 infertility IAGP N RGD:5509061 20180315 MGI PMID:28811219 1618182 Tnrc6b trinucleotide repeat containing 6b gene MP:0001925 male infertility IEA N RGD:5509061 20240523 MGI 1618182 Tnrc6b trinucleotide repeat containing 6b gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220519 MGI 1618182 Tnrc6b trinucleotide repeat containing 6b gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20221215 MGI 1618182 Tnrc6b trinucleotide repeat containing 6b gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20180315 MGI PMID:28811219 1618182 Tnrc6b trinucleotide repeat containing 6b gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180315 MGI PMID:28811219 1618182 Tnrc6b trinucleotide repeat containing 6b gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220519 MGI 1618183 Fbxw10 F-box and WD-40 domain protein 10 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1618183 Fbxw10 F-box and WD-40 domain protein 10 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1618185 Col28a1 collagen, type XXVIII, alpha 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20231207 MGI 1618185 Col28a1 collagen, type XXVIII, alpha 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 1618186 Pdzd7 PDZ domain containing 7 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:24334608 1618186 Pdzd7 PDZ domain containing 7 gene MP:0001967 deafness IAGP N RGD:5509061 20160929 MGI PMID:27534441 1618186 Pdzd7 PDZ domain containing 7 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24334608 1618186 Pdzd7 PDZ domain containing 7 gene MP:0004414 decreased cochlear microphonics IAGP N RGD:5509061 20141003 MGI PMID:24334608 1618186 Pdzd7 PDZ domain containing 7 gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20141003 MGI PMID:24334608 1618186 Pdzd7 PDZ domain containing 7 gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24334608 1618186 Pdzd7 PDZ domain containing 7 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:24334608 1618186 Pdzd7 PDZ domain containing 7 gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:24334608 1618186 Pdzd7 PDZ domain containing 7 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:24334608 1618186 Pdzd7 PDZ domain containing 7 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:24334608 1618186 Pdzd7 PDZ domain containing 7 gene MP:0030961 abnormal outer hair cell kinocilium location or orientation IAGP N RGD:5509061 20190725 MGI PMID:24334608 1618188 Iffo2 intermediate filament family orphan 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20201022 MGI 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20210429 MGI PMID:32923640 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20210429 MGI PMID:32923640 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20210429 MGI PMID:32923640 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20210429 MGI PMID:32923640 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20201022 MGI 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20210429 MGI PMID:32923640 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210128 MGI 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20210429 MGI PMID:32923640 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38697008 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20201022 MGI 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 1618192 Nemp1 nuclear envelope integral membrane protein 1 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20210429 MGI PMID:32923640 1618193 Metrnl meteorin, glial cell differentiation regulator-like gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20191107 MGI PMID:30464051 1618193 Metrnl meteorin, glial cell differentiation regulator-like gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20191107 MGI PMID:30464051 1618193 Metrnl meteorin, glial cell differentiation regulator-like gene MP:0001860 liver inflammation IAGP N RGD:5509061 20191107 MGI PMID:30464051 1618193 Metrnl meteorin, glial cell differentiation regulator-like gene MP:0002494 increased IgM level IAGP N RGD:5509061 20191107 MGI PMID:30464051 1618193 Metrnl meteorin, glial cell differentiation regulator-like gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20191107 MGI PMID:30464051 1618193 Metrnl meteorin, glial cell differentiation regulator-like gene MP:0009080 uterus inflammation IAGP N RGD:5509061 20191107 MGI PMID:30464051 1618193 Metrnl meteorin, glial cell differentiation regulator-like gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20191107 MGI PMID:30464051 1618197 Wdr11 WD repeat domain 11 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0000433 microcephaly IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0000547 short limbs IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0000564 syndactyly IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20210128 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0001127 small ovary IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0001261 obese IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0002188 small heart IEA N RGD:5509061 20201022 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0002637 small uterus IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20201022 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20201022 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0003550 short perineum IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20201022 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0003817 abnormal pituitary diverticulum morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0004391 abnormal respiratory conducting tube morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0004592 small mandible IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0005163 cyclopia IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0005188 small penis IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0005313 absent adrenal gland IEA N RGD:5509061 20210826 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0006087 increased body mass index IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0006305 abnormal optic eminence morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0006306 abnormal nasal pit morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0008940 delayed balanopreputial separation IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0009203 external male genitalia hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0009229 abnormal neurohypophysis median eminence morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0010059 olfactory bulb hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0011130 absent tertiary ovarian follicles IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0011281 abnormal olfactory epithelium cilium morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0011999 abnormal tail length IEA N RGD:5509061 20231207 MGI 1618197 Wdr11 WD repeat domain 11 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0013350 Rathke's pouch hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0030198 nasal septum hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:29263200 1618197 Wdr11 WD repeat domain 11 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:29263200 1618199 Grhl1 grainyhead like transcription factor 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20200310 MGI PMID:18288204 1618199 Grhl1 grainyhead like transcription factor 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20200310 MGI PMID:18288204 1618199 Grhl1 grainyhead like transcription factor 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20200310 MGI PMID:18288204 1618199 Grhl1 grainyhead like transcription factor 1 gene MP:0000418 focal hair loss IEA N RGD:5509061 20111116 MGI 1618199 Grhl1 grainyhead like transcription factor 1 gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20200310 MGI PMID:18288204 1618199 Grhl1 grainyhead like transcription factor 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20200310 MGI PMID:18288204 1618199 Grhl1 grainyhead like transcription factor 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20200310 MGI PMID:26975724 1618199 Grhl1 grainyhead like transcription factor 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20200310 MGI PMID:18288204 1618199 Grhl1 grainyhead like transcription factor 1 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 1618199 Grhl1 grainyhead like transcription factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:18288204 1618199 Grhl1 grainyhead like transcription factor 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20200310 MGI PMID:26975724 1618199 Grhl1 grainyhead like transcription factor 1 gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20200310 MGI PMID:26975724 1618199 Grhl1 grainyhead like transcription factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:26975724 1618200 Nhs NHS actin remodeling regulator gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:8282045 1618200 Nhs NHS actin remodeling regulator gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:2272505 1618200 Nhs NHS actin remodeling regulator gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:8282045 1618200 Nhs NHS actin remodeling regulator gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1618200 Nhs NHS actin remodeling regulator gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 1618200 Nhs NHS actin remodeling regulator gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:8282045 1618200 Nhs NHS actin remodeling regulator gene MP:0003236 abnormal lens capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:8282045 1618200 Nhs NHS actin remodeling regulator gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20141003 MGI PMID:8282045 1618200 Nhs NHS actin remodeling regulator gene MP:0010263 total cataract IEA N RGD:5509061 20111116 MGI 1618200 Nhs NHS actin remodeling regulator gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20211021 MGI 1618200 Nhs NHS actin remodeling regulator gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:8282045 1618201 Scml1 Scm polycomb group protein like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20191017 MGI PMID:27165042 1618201 Scml1 Scm polycomb group protein like 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20191017 MGI PMID:27165042 1618204 Slu7 SLU7 splicing factor homolog (S. cerevisiae) gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1618204 Slu7 SLU7 splicing factor homolog (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1618205 Il17rc interleukin 17 receptor C gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1618205 Il17rc interleukin 17 receptor C gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1618205 Il17rc interleukin 17 receptor C gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20230601 MGI 1618205 Il17rc interleukin 17 receptor C gene MP:0001258 decreased body length IEA N RGD:5509061 20230601 MGI 1618205 Il17rc interleukin 17 receptor C gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:20231694 1618205 Il17rc interleukin 17 receptor C gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1618205 Il17rc interleukin 17 receptor C gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1618205 Il17rc interleukin 17 receptor C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18264109 1618205 Il17rc interleukin 17 receptor C gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20230601 MGI 1618205 Il17rc interleukin 17 receptor C gene MP:0002989 small kidney IEA N RGD:5509061 20230601 MGI 1618205 Il17rc interleukin 17 receptor C gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:20231694 1618205 Il17rc interleukin 17 receptor C gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:20231694 1618205 Il17rc interleukin 17 receptor C gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:20231694 1618233 Zfp91 zinc finger protein 91 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1618233 Zfp91 zinc finger protein 91 gene MP:0001258 decreased body length IEA N RGD:5509061 20201022 MGI 1618233 Zfp91 zinc finger protein 91 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1618233 Zfp91 zinc finger protein 91 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210128 MGI 1618233 Zfp91 zinc finger protein 91 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1618233 Zfp91 zinc finger protein 91 gene MP:0003717 pallor IEA N RGD:5509061 20210128 MGI 1618233 Zfp91 zinc finger protein 91 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20240620 MGI PMID:33355624 1618233 Zfp91 zinc finger protein 91 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20240620 MGI PMID:33355624 1618233 Zfp91 zinc finger protein 91 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20240620 MGI PMID:33355624 1618233 Zfp91 zinc finger protein 91 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20240620 MGI PMID:33355624 1618233 Zfp91 zinc finger protein 91 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20240620 MGI PMID:33355624 1618233 Zfp91 zinc finger protein 91 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20240620 MGI PMID:33355624 1618233 Zfp91 zinc finger protein 91 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200514 MGI 1618233 Zfp91 zinc finger protein 91 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20210128 MGI 1618234 Mcf2 mcf.2 transforming sequence gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:11940671 1618235 Ccdc86 coiled-coil domain containing 86 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19528538 1618235 Ccdc86 coiled-coil domain containing 86 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19528538 1618235 Ccdc86 coiled-coil domain containing 86 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19528538 1618236 Epsti1 epithelial stromal interaction 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20191017 MGI PMID:29217193 1618236 Epsti1 epithelial stromal interaction 1 gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20191017 MGI PMID:29217193 1618237 Rnpepl1 arginyl aminopeptidase (aminopeptidase B)-like 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1618237 Rnpepl1 arginyl aminopeptidase (aminopeptidase B)-like 1 gene MP:0001304 cataract IEA N RGD:5509061 20220519 MGI 1618237 Rnpepl1 arginyl aminopeptidase (aminopeptidase B)-like 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1618237 Rnpepl1 arginyl aminopeptidase (aminopeptidase B)-like 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220811 MGI 1618240 Kank1 KN motif and ankyrin repeat domains 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1618240 Kank1 KN motif and ankyrin repeat domains 1 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 1618241 AW112010 expressed sequence AW112010 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20191219 MGI PMID:30542152 1618241 AW112010 expressed sequence AW112010 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20191219 MGI PMID:30542152 1618241 AW112010 expressed sequence AW112010 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20191219 MGI PMID:30542152 1618241 AW112010 expressed sequence AW112010 gene MP:0008648 decreased circulating interleukin-12b level IAGP N RGD:5509061 20191219 MGI PMID:30542152 1618241 AW112010 expressed sequence AW112010 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20191219 MGI PMID:30542152 1618241 AW112010 expressed sequence AW112010 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20191219 MGI PMID:30542152 1618241 AW112010 expressed sequence AW112010 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20191219 MGI PMID:30542152 1618242 Gbf1 golgi-specific brefeldin A-resistance factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000433 microcephaly IEA N RGD:5509061 20141003 MGI 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000445 short snout IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000445 short snout IAGP N RGD:5509061 20221201 MGI PMID:24689077 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000447 flattened snout IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000592 short tail IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20220331 MGI PMID:34597683 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20220331 MGI PMID:34597683 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20141003 MGI PMID:21276947 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:19706528 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:19706528 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:19706528 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:19706528 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0002639 micrognathia IEA N RGD:5509061 20141003 MGI 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20220331 MGI PMID:34597683 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:19706528 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0004524 short cochlear hair cell stereocilia IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:19706528 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20220331 MGI PMID:34597683 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0008727 increased heart right atrium size IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20221201 MGI PMID:24689077 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221201 MGI PMID:24689077 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:19706528 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221201 MGI PMID:24689077 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221201 MGI PMID:24689077 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221201 MGI PMID:24689077 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0009897 decreased maxillary shelf size IAGP N RGD:5509061 20221201 MGI PMID:24689077 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0009909 bifid tongue IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20141003 MGI 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21276947 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19706528 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20141003 MGI PMID:19706528 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0011666 double outlet right ventricle, ventricular defect committed to aorta IEA N RGD:5509061 20141003 MGI 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0012285 misaligned sternebrae IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0013179 wavy tail IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20160428 MGI PMID:19706528 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0013895 abnormal eyelid cilium morphology IAGP N RGD:5509061 20171228 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0020301 short tongue IAGP N RGD:5509061 20150903 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20220331 MGI PMID:34597683 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:24689077 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0030049 prominent forehead IAGP N RGD:5509061 20170921 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0030475 fused lower incisors IAGP N RGD:5509061 20171228 MGI PMID:25190059 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:24689077 1618248 Prickle1 prickle planar cell polarity protein 1 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20221201 MGI PMID:24689077 1618250 Vipas39 VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog gene MP:0000414 alopecia IAGP N RGD:5509061 20170126 MGI PMID:27435297 1618250 Vipas39 VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog gene MP:0001192 scaly skin IAGP N RGD:5509061 20170126 MGI PMID:27435297 1618250 Vipas39 VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog gene MP:0003853 dry skin IAGP N RGD:5509061 20170126 MGI PMID:27435297 1618250 Vipas39 VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20170126 MGI PMID:27435297 1618252 Sptssa serine palmitoyltransferase, small subunit A gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191128 MGI 1618252 Sptssa serine palmitoyltransferase, small subunit A gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191128 MGI 1618252 Sptssa serine palmitoyltransferase, small subunit A gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191128 MGI 1618252 Sptssa serine palmitoyltransferase, small subunit A gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1618252 Sptssa serine palmitoyltransferase, small subunit A gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160421 MGI 1618252 Sptssa serine palmitoyltransferase, small subunit A gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1618252 Sptssa serine palmitoyltransferase, small subunit A gene MP:0009331 absent primitive node IEA N RGD:5509061 20191128 MGI 1618252 Sptssa serine palmitoyltransferase, small subunit A gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1618252 Sptssa serine palmitoyltransferase, small subunit A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1618252 Sptssa serine palmitoyltransferase, small subunit A gene MP:0012724 absent head fold IEA N RGD:5509061 20191128 MGI 1618252 Sptssa serine palmitoyltransferase, small subunit A gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20160804 MGI 1618252 Sptssa serine palmitoyltransferase, small subunit A gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1618253 Ttc7b tetratricopeptide repeat domain 7B gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1618253 Ttc7b tetratricopeptide repeat domain 7B gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1618253 Ttc7b tetratricopeptide repeat domain 7B gene MP:0002080 prenatal lethality IEA N RGD:5509061 20210128 MGI 1618253 Ttc7b tetratricopeptide repeat domain 7B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1618253 Ttc7b tetratricopeptide repeat domain 7B gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1618254 Pik3r6 phosphoinositide-3-kinase regulatory subunit 5 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20170713 MGI PMID:25605974 1618254 Pik3r6 phosphoinositide-3-kinase regulatory subunit 5 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20170713 MGI PMID:25605974 1618254 Pik3r6 phosphoinositide-3-kinase regulatory subunit 5 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20170713 MGI PMID:25605974 1618254 Pik3r6 phosphoinositide-3-kinase regulatory subunit 5 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20170713 MGI PMID:25605974 1618257 Snx25 sorting nexin 25 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1618257 Snx25 sorting nexin 25 gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20201022 MGI 1618257 Snx25 sorting nexin 25 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1618258 Eif3m eukaryotic translation initiation factor 3, subunit M gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:24003236 1618258 Eif3m eukaryotic translation initiation factor 3, subunit M gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24003236 1618258 Eif3m eukaryotic translation initiation factor 3, subunit M gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24003236 1618258 Eif3m eukaryotic translation initiation factor 3, subunit M gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:24003236 1618258 Eif3m eukaryotic translation initiation factor 3, subunit M gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:24003236 1618258 Eif3m eukaryotic translation initiation factor 3, subunit M gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24003236 1618258 Eif3m eukaryotic translation initiation factor 3, subunit M gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:24003236 1618258 Eif3m eukaryotic translation initiation factor 3, subunit M gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24003236 1618258 Eif3m eukaryotic translation initiation factor 3, subunit M gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24003236 1618260 Nrg4 neuregulin 4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1618261 Phip pleckstrin homology domain interacting protein gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:20816727 1618261 Phip pleckstrin homology domain interacting protein gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1618261 Phip pleckstrin homology domain interacting protein gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20201231 MGI 1618261 Phip pleckstrin homology domain interacting protein gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20816727 1618261 Phip pleckstrin homology domain interacting protein gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1618261 Phip pleckstrin homology domain interacting protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20816727 1618261 Phip pleckstrin homology domain interacting protein gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1618261 Phip pleckstrin homology domain interacting protein gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200402 MGI 1618261 Phip pleckstrin homology domain interacting protein gene MP:0001891 hydrocephaly IEA N RGD:5509061 20200402 MGI 1618261 Phip pleckstrin homology domain interacting protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20816727 1618261 Phip pleckstrin homology domain interacting protein gene MP:0002637 small uterus IEA N RGD:5509061 20200402 MGI 1618261 Phip pleckstrin homology domain interacting protein gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20816727 1618261 Phip pleckstrin homology domain interacting protein gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 1618261 Phip pleckstrin homology domain interacting protein gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:20816727 1618261 Phip pleckstrin homology domain interacting protein gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220519 MGI 1618261 Phip pleckstrin homology domain interacting protein gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20816727 1618261 Phip pleckstrin homology domain interacting protein gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20816727 1618261 Phip pleckstrin homology domain interacting protein gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20816727 1618261 Phip pleckstrin homology domain interacting protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20816727 1618261 Phip pleckstrin homology domain interacting protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1618261 Phip pleckstrin homology domain interacting protein gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20200402 MGI 1618263 Usp54 ubiquitin specific peptidase 54 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1618263 Usp54 ubiquitin specific peptidase 54 gene MP:0000274 enlarged heart IEA N RGD:5509061 20160811 MGI 1618263 Usp54 ubiquitin specific peptidase 54 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1618263 Usp54 ubiquitin specific peptidase 54 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20210520 MGI 1618263 Usp54 ubiquitin specific peptidase 54 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1618263 Usp54 ubiquitin specific peptidase 54 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1618263 Usp54 ubiquitin specific peptidase 54 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160421 MGI 1618263 Usp54 ubiquitin specific peptidase 54 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20170105 MGI 1618263 Usp54 ubiquitin specific peptidase 54 gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20181227 MGI 1618263 Usp54 ubiquitin specific peptidase 54 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 1618263 Usp54 ubiquitin specific peptidase 54 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20160421 MGI 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0001925 male infertility IAGP N RGD:5509061 20220217 MGI PMID:34792097 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0001925 male infertility IAGP N RGD:5509061 20230413 MGI PMID:35387802 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220217 MGI PMID:34792097 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230413 MGI PMID:35387802 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220217 MGI PMID:34792097 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230413 MGI PMID:35387802 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20201022 MGI 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20220217 MGI PMID:34792097 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20230413 MGI PMID:35387802 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220217 MGI PMID:34792097 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20230413 MGI PMID:35387802 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220217 MGI PMID:34792097 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220217 MGI PMID:34792097 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20230413 MGI PMID:35387802 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220217 MGI PMID:34792097 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20230413 MGI PMID:35387802 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0009241 thick sperm flagellum IAGP N RGD:5509061 20220217 MGI PMID:34792097 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220217 MGI PMID:34792097 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20230413 MGI PMID:35387802 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20230413 MGI PMID:35387802 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20230413 MGI PMID:35387802 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220217 MGI PMID:34792097 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20230413 MGI PMID:35387802 1618265 Cfap61 cilia and flagella associated protein 61 gene MP:0031438 abnormal sperm radial spoke morphology IAGP N RGD:5509061 20220915 MGI PMID:34792097 1618266 Pabir2 PABIR family member 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0000692 small spleen IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0002188 small heart IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0002691 small stomach IEA N RGD:5509061 20230601 MGI 1618266 Pabir2 PABIR family member 2 gene MP:0013129 abnormal tooth color IEA N RGD:5509061 20230601 MGI 1618267 Filip1l filamin A interacting protein 1-like gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20240321 MGI PMID:34417201 1618267 Filip1l filamin A interacting protein 1-like gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20240321 MGI PMID:34417201 1618267 Filip1l filamin A interacting protein 1-like gene MP:0013799 abnormal intestinal goblet cell physiology IAGP N RGD:5509061 20240321 MGI PMID:34417201 1618267 Filip1l filamin A interacting protein 1-like gene MP:0014221 increased colon goblet cell number IAGP N RGD:5509061 20240321 MGI PMID:34417201 1618273 Tmem116 transmembrane protein 116 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1618273 Tmem116 transmembrane protein 116 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1618273 Tmem116 transmembrane protein 116 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20210128 MGI 1618273 Tmem116 transmembrane protein 116 gene MP:0001262 decreased body weight IEA N RGD:5509061 20210520 MGI 1618273 Tmem116 transmembrane protein 116 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20220811 MGI 1618273 Tmem116 transmembrane protein 116 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20230601 MGI 1618273 Tmem116 transmembrane protein 116 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 1618273 Tmem116 transmembrane protein 116 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20181227 MGI 1618273 Tmem116 transmembrane protein 116 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 1618273 Tmem116 transmembrane protein 116 gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 1618275 Med13l mediator complex subunit 13-like gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20230119 MGI 1618275 Med13l mediator complex subunit 13-like gene MP:0001297 microphthalmia IEA N RGD:5509061 20230119 MGI 1618275 Med13l mediator complex subunit 13-like gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20230601 MGI 1618275 Med13l mediator complex subunit 13-like gene MP:0001785 edema IEA N RGD:5509061 20230601 MGI 1618275 Med13l mediator complex subunit 13-like gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20230119 MGI 1618275 Med13l mediator complex subunit 13-like gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230119 MGI 1618276 Usp31 ubiquitin specific peptidase 31 gene MP:0000745 tremors IEA N RGD:5509061 20210128 MGI 1618276 Usp31 ubiquitin specific peptidase 31 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1618276 Usp31 ubiquitin specific peptidase 31 gene MP:0001406 abnormal gait IEA N RGD:5509061 20200514 MGI 1618276 Usp31 ubiquitin specific peptidase 31 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1618276 Usp31 ubiquitin specific peptidase 31 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20200514 MGI 1618276 Usp31 ubiquitin specific peptidase 31 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1618276 Usp31 ubiquitin specific peptidase 31 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20211021 MGI 1618276 Usp31 ubiquitin specific peptidase 31 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20210128 MGI 1618276 Usp31 ubiquitin specific peptidase 31 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1618276 Usp31 ubiquitin specific peptidase 31 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 1618277 Coa5 cytochrome C oxidase assembly factor 5 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 1618277 Coa5 cytochrome C oxidase assembly factor 5 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20221215 MGI 1618277 Coa5 cytochrome C oxidase assembly factor 5 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1618277 Coa5 cytochrome C oxidase assembly factor 5 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20160811 MGI 1618277 Coa5 cytochrome C oxidase assembly factor 5 gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1618277 Coa5 cytochrome C oxidase assembly factor 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1618277 Coa5 cytochrome C oxidase assembly factor 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1618277 Coa5 cytochrome C oxidase assembly factor 5 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0000484 abnormal pulmonary artery morphology IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0000562 polydactyly IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0000644 dextrocardia IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0001178 pulmonary hypoplasia IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0002639 micrognathia IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0003321 tracheoesophageal fistula IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0004133 heterotaxia IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0005170 cleft upper lip IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0009743 preaxial polydactyly IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0010406 common atrium IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0010885 absent trachea IEA N RGD:5509061 20170209 MGI 1618278 Cplane2 ciliogenesis and planar polarity effector 2 gene MP:0011254 superior-inferior ventricles IEA N RGD:5509061 20170209 MGI 1618280 Lamp5 lysosomal-associated membrane protein family, member 5 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20240314 MGI PMID:35780436 1618280 Lamp5 lysosomal-associated membrane protein family, member 5 gene MP:0002083 premature death IAGP N RGD:5509061 20240314 MGI PMID:35780436 1618280 Lamp5 lysosomal-associated membrane protein family, member 5 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20240314 MGI PMID:35780436 1618280 Lamp5 lysosomal-associated membrane protein family, member 5 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20240314 MGI PMID:35780436 1618280 Lamp5 lysosomal-associated membrane protein family, member 5 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20240314 MGI PMID:35780436 1618280 Lamp5 lysosomal-associated membrane protein family, member 5 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20240314 MGI PMID:35780436 1618280 Lamp5 lysosomal-associated membrane protein family, member 5 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1618280 Lamp5 lysosomal-associated membrane protein family, member 5 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20240314 MGI PMID:35780436 1618280 Lamp5 lysosomal-associated membrane protein family, member 5 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20240314 MGI PMID:35780436 1618280 Lamp5 lysosomal-associated membrane protein family, member 5 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20240314 MGI PMID:35780436 1618280 Lamp5 lysosomal-associated membrane protein family, member 5 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1618280 Lamp5 lysosomal-associated membrane protein family, member 5 gene MP:0021020 neurite dystrophy IAGP N RGD:5509061 20240314 MGI PMID:35780436 1618281 Slc35d3 solute carrier family 35, member D3 gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20200310 MGI PMID:17062724 1618283 Prex2 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2 gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20220519 MGI 1618283 Prex2 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18334636 1618283 Prex2 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18334636 1618283 Prex2 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18334636 1618283 Prex2 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18334636 1618283 Prex2 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:18334636 1618283 Prex2 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18334636 1618283 Prex2 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:18334636 1618283 Prex2 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:24367090 1618283 Prex2 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:24367090 1618283 Prex2 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:24367090 1618283 Prex2 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18334636 1618284 Faxc failed axon connections homolog gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1618284 Faxc failed axon connections homolog gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1618285 Arhgap15 Rho GTPase activating protein 15 gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21551229 1618285 Arhgap15 Rho GTPase activating protein 15 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21551229 1618285 Arhgap15 Rho GTPase activating protein 15 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21551229 1618285 Arhgap15 Rho GTPase activating protein 15 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21551229 1618285 Arhgap15 Rho GTPase activating protein 15 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:21551229 1618285 Arhgap15 Rho GTPase activating protein 15 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:21551229 1618285 Arhgap15 Rho GTPase activating protein 15 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:21551229 1618285 Arhgap15 Rho GTPase activating protein 15 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21551229 1618285 Arhgap15 Rho GTPase activating protein 15 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21551229 1618290 Morn3 MORN repeat containing 3 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 1618291 Tmem65 transmembrane protein 65 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230119 MGI 1618295 Meikin meiotic kinetochore factor gene MP:0001925 male infertility IAGP N RGD:5509061 20151015 MGI PMID:25533956 1618295 Meikin meiotic kinetochore factor gene MP:0001926 female infertility IAGP N RGD:5509061 20151015 MGI PMID:25533956 1618295 Meikin meiotic kinetochore factor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20151015 MGI PMID:25533956 1618295 Meikin meiotic kinetochore factor gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20151015 MGI PMID:25533956 1618295 Meikin meiotic kinetochore factor gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20151015 MGI PMID:25533956 1618295 Meikin meiotic kinetochore factor gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20151015 MGI PMID:25533956 1618295 Meikin meiotic kinetochore factor gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20151015 MGI PMID:25533956 1618295 Meikin meiotic kinetochore factor gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20151015 MGI PMID:25533956 1618295 Meikin meiotic kinetochore factor gene MP:0014443 impaired polar body extrusion IAGP N RGD:5509061 20240509 MGI PMID:25533956 1618297 Vgll3 vestigial like family member 3 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220519 MGI 1618297 Vgll3 vestigial like family member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:31138678 1618297 Vgll3 vestigial like family member 3 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20230601 MGI 1618297 Vgll3 vestigial like family member 3 gene MP:0031216 decreased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20230921 MGI PMID:36754961 1618304 Pebp4 phosphatidylethanolamine binding protein 4 gene MP:0001258 decreased body length IEA N RGD:5509061 20240523 MGI 1618307 Lsm11 U7 snRNP-specific Sm-like protein LSM11 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1618308 Ccpg1 cell cycle progression 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20190221 MGI PMID:29290589 1618308 Ccpg1 cell cycle progression 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20190221 MGI PMID:29290589 1618308 Ccpg1 cell cycle progression 1 gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20190221 MGI PMID:29290589 1618308 Ccpg1 cell cycle progression 1 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20181227 MGI 1618308 Ccpg1 cell cycle progression 1 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20190221 MGI PMID:29290589 1618308 Ccpg1 cell cycle progression 1 gene MP:0009147 abnormal pancreatic acinar cell physiology IAGP N RGD:5509061 20190221 MGI PMID:29290589 1618308 Ccpg1 cell cycle progression 1 gene MP:0009148 pancreas necrosis IAGP N RGD:5509061 20190221 MGI PMID:29290589 1618308 Ccpg1 cell cycle progression 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20190221 MGI PMID:29290589 1618308 Ccpg1 cell cycle progression 1 gene MP:0010148 abnormal exocrine pancreas physiology IAGP N RGD:5509061 20190221 MGI PMID:29290589 1618308 Ccpg1 cell cycle progression 1 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20181227 MGI 1618308 Ccpg1 cell cycle progression 1 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20190221 MGI PMID:29290589 1618308 Ccpg1 cell cycle progression 1 gene MP:0030938 abnormal reticulophagy IAGP N RGD:5509061 20190711 MGI PMID:29290589 1618317 Zfp558 zinc finger protein 558 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1618317 Zfp558 zinc finger protein 558 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 1618317 Zfp558 zinc finger protein 558 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210520 MGI 1618317 Zfp558 zinc finger protein 558 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210520 MGI 1618317 Zfp558 zinc finger protein 558 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20190502 MGI 1618317 Zfp558 zinc finger protein 558 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 1618318 Cimip1 ciliary microtubule inner protein 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20231207 MGI 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180201 MGI PMID:22367054 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:22367054 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:23064362 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20180201 MGI PMID:22367054 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20180201 MGI PMID:23064362 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20180201 MGI PMID:17657313 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20180201 MGI PMID:22367054 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20180201 MGI PMID:12196292 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:12196292 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:17911589 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20180201 MGI PMID:17657313 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20180201 MGI PMID:23334413 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180201 MGI PMID:22367054 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20180201 MGI PMID:17657313 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20180201 MGI PMID:17911589 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20180201 MGI PMID:17911589 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0004031 insulitis IAGP N RGD:5509061 20180201 MGI PMID:17911589 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20180201 MGI PMID:17911589 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0005000 abnormal immune tolerance IAGP N RGD:5509061 20180201 MGI PMID:17657313 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20180201 MGI PMID:23064362 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20180201 MGI PMID:22615130 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0005044 sepsis IAGP N RGD:5509061 20180201 MGI PMID:16116220 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20180201 MGI PMID:17389237 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20180201 MGI PMID:12196292 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20180201 MGI PMID:17446931 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0005150 cachexia IAGP N RGD:5509061 20180201 MGI PMID:17911589 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20180201 MGI PMID:17911589 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20180201 MGI PMID:15644449 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20180201 MGI PMID:12196292 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20180201 MGI PMID:12196292 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20180201 MGI PMID:12196292 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20180201 MGI PMID:15644449 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20180201 MGI PMID:15944318 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20180201 MGI PMID:16116220 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20180201 MGI PMID:17911589 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20180201 MGI PMID:18591406 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20180201 MGI PMID:22367054 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008240 abnormal spleen marginal zone macrophage morphology IAGP N RGD:5509061 20180201 MGI PMID:17657313 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008241 abnormal metallophilic macrophage morphology IAGP N RGD:5509061 20180201 MGI PMID:17657313 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20180201 MGI PMID:18591406 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20180201 MGI PMID:23064362 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20180201 MGI PMID:17911589 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20180201 MGI PMID:17911589 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20180201 MGI PMID:15644449 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20180201 MGI PMID:18591406 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20180201 MGI PMID:15644449 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008618 decreased circulating interleukin-12 level IAGP N RGD:5509061 20180201 MGI PMID:15644449 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20180201 MGI PMID:17389237 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20180201 MGI PMID:23064362 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20180201 MGI PMID:15644449 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20180201 MGI PMID:22367054 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180201 MGI PMID:23064362 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180201 MGI PMID:16116220 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20180201 MGI PMID:22367054 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20180201 MGI PMID:15644449 1618321 1700016L21Rik RIKEN cDNA 1700016L21 gene gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:18591406 1618324 Tektl1 tektin like 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240627 MGI PMID:38835510 1618326 Tex19.2 testis expressed gene 19.2 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20180201 MGI PMID:28254886 1618326 Tex19.2 testis expressed gene 19.2 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20180201 MGI PMID:28254886 1618326 Tex19.2 testis expressed gene 19.2 gene MP:0001925 male infertility IAGP N RGD:5509061 20180201 MGI PMID:28254886 1618326 Tex19.2 testis expressed gene 19.2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20180201 MGI PMID:28254886 1618326 Tex19.2 testis expressed gene 19.2 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20180201 MGI PMID:28254886 1618326 Tex19.2 testis expressed gene 19.2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180201 MGI PMID:28254886 1618326 Tex19.2 testis expressed gene 19.2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20180201 MGI PMID:28254886 1618326 Tex19.2 testis expressed gene 19.2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20180201 MGI PMID:28254886 1618326 Tex19.2 testis expressed gene 19.2 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20180201 MGI PMID:28254886 1618326 Tex19.2 testis expressed gene 19.2 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20180201 MGI PMID:28254886 1618329 Mmrn1 multimerin 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1618329 Mmrn1 multimerin 1 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20201022 MGI 1618330 4921539E11Rik RIKEN cDNA 4921539E11 gene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20211223 MGI PMID:34290169 1618332 Speer4f1 spermatogenesis associated glutamate (E)-rich protein 4F1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1618332 Speer4f1 spermatogenesis associated glutamate (E)-rich protein 4F1 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1618332 Speer4f1 spermatogenesis associated glutamate (E)-rich protein 4F1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1618332 Speer4f1 spermatogenesis associated glutamate (E)-rich protein 4F1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20181227 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20181227 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20210729 MGI PMID:30190432 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0000961 abnormal dorsal root ganglion morphology IEA N RGD:5509061 20170504 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20171116 MGI PMID:26715742 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20171116 MGI PMID:26715742 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20210520 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0001304 cataract IEA N RGD:5509061 20210520 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0001306 small lens IEA N RGD:5509061 20170504 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0001307 fused cornea and lens IEA N RGD:5509061 20210520 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210520 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0001314 cornea opacity IEA N RGD:5509061 20210520 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0001512 trunk curl IEA N RGD:5509061 20201231 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170504 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20181227 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20201022 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0003443 increased circulating glycerol level IEA N RGD:5509061 20211021 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20181227 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20210729 MGI PMID:30190432 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0005477 increased circulating thyroxine level IEA N RGD:5509061 20211021 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20201022 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20170504 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20181227 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20171116 MGI PMID:26715742 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20210729 MGI PMID:30190432 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0008346 increased gamma-delta T cell number IEA N RGD:5509061 20181227 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0008922 abnormal cervical rib IEA N RGD:5509061 20170504 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0008986 abnormal liver parenchyma morphology IEA N RGD:5509061 20170504 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0010484 bicuspid aortic valve IEA N RGD:5509061 20170504 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20171116 MGI PMID:26715742 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0014087 retrolental blood IEA N RGD:5509061 20180628 MGI 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0020581 abnormal neuron polarity IAGP N RGD:5509061 20210729 MGI PMID:30190432 1618338 Camsap3 calmodulin regulated spectrin-associated protein family, member 3 gene MP:0020850 abnormal microtubule cytoskeleton morphology IAGP N RGD:5509061 20210729 MGI PMID:30190432 1618339 Hddc2 HD domain containing 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210826 MGI 1618339 Hddc2 HD domain containing 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1618339 Hddc2 HD domain containing 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20200310 MGI 1618339 Hddc2 HD domain containing 2 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1618339 Hddc2 HD domain containing 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1618339 Hddc2 HD domain containing 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20200310 MGI 1618339 Hddc2 HD domain containing 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210826 MGI 1618339 Hddc2 HD domain containing 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1618339 Hddc2 HD domain containing 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1618339 Hddc2 HD domain containing 2 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20200310 MGI 1618339 Hddc2 HD domain containing 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220811 MGI PMID:29659949 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20210128 MGI 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20141003 MGI 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20160421 MGI 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0001922 reduced male fertility IEA N RGD:5509061 20141003 MGI 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220811 MGI PMID:29659949 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0001925 male infertility IAGP N RGD:5509061 20220811 MGI PMID:29659949 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220811 MGI PMID:29659949 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220811 MGI PMID:29659949 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20220811 MGI PMID:29659949 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20220811 MGI PMID:29659949 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220811 MGI PMID:29659949 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20141003 MGI 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20220811 MGI PMID:29659949 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220811 MGI PMID:29659949 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20220811 MGI PMID:29659949 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0011977 abnormal sodium ion homeostasis IAGP N RGD:5509061 20220811 MGI PMID:29659949 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1618341 Emc10 ER membrane protein complex subunit 10 gene MP:0031393 abnormal bicarbonate homeostasis IAGP N RGD:5509061 20220811 MGI PMID:29659949 1618342 Cdk3 cyclin dependent kinase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151217 MGI PMID:11172011 1618346 Mlip muscular LMNA-interacting protein gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20170907 MGI PMID:26436652 1618346 Mlip muscular LMNA-interacting protein gene MP:0002083 premature death IAGP N RGD:5509061 20170907 MGI PMID:26436652 1618346 Mlip muscular LMNA-interacting protein gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20170907 MGI PMID:26436652 1618346 Mlip muscular LMNA-interacting protein gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170907 MGI PMID:26436652 1618346 Mlip muscular LMNA-interacting protein gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20170907 MGI PMID:26436652 1618346 Mlip muscular LMNA-interacting protein gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20170907 MGI PMID:26436652 1618346 Mlip muscular LMNA-interacting protein gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20170907 MGI PMID:26436652 1618346 Mlip muscular LMNA-interacting protein gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20170907 MGI PMID:26436652 1618346 Mlip muscular LMNA-interacting protein gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20170907 MGI PMID:26436652 1618346 Mlip muscular LMNA-interacting protein gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170907 MGI PMID:26436652 1618346 Mlip muscular LMNA-interacting protein gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:26436652 1618348 Fam83g family with sequence similarity 83, member G gene MP:0000410 waved hair IEA N RGD:5509061 20141003 MGI 1618348 Fam83g family with sequence similarity 83, member G gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1618348 Fam83g family with sequence similarity 83, member G gene MP:0002608 increased hematocrit IEA N RGD:5509061 20141003 MGI 1618348 Fam83g family with sequence similarity 83, member G gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 1618348 Fam83g family with sequence similarity 83, member G gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20141003 MGI 1618349 Enho energy homeostasis associated gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20151015 MGI PMID:25074942 1618349 Enho energy homeostasis associated gene MP:0001260 increased body weight IAGP N RGD:5509061 20160811 MGI PMID:22318315 1618349 Enho energy homeostasis associated gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20151015 MGI PMID:25074942 1618349 Enho energy homeostasis associated gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160811 MGI PMID:22318315 1618349 Enho energy homeostasis associated gene MP:0001405 impaired coordination IAGP N RGD:5509061 20151015 MGI PMID:25074942 1618349 Enho energy homeostasis associated gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20160811 MGI PMID:22318315 1618349 Enho energy homeostasis associated gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160811 MGI PMID:22318315 1618349 Enho energy homeostasis associated gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160811 MGI PMID:22318315 1618349 Enho energy homeostasis associated gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20151015 MGI PMID:25074942 1618349 Enho energy homeostasis associated gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20160811 MGI PMID:22318315 1618349 Enho energy homeostasis associated gene MP:0005331 insulin resistance IAGP N RGD:5509061 20160811 MGI PMID:22318315 1618349 Enho energy homeostasis associated gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20160811 MGI PMID:22318315 1618349 Enho energy homeostasis associated gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20160811 MGI PMID:22318315 1618349 Enho energy homeostasis associated gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20160811 MGI PMID:22318315 1618349 Enho energy homeostasis associated gene MP:0011940 decreased food intake IAGP N RGD:5509061 20151015 MGI PMID:25074942 1618349 Enho energy homeostasis associated gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20160811 MGI PMID:22318315 1618349 Enho energy homeostasis associated gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20160811 MGI PMID:22318315 1618349 Enho energy homeostasis associated gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20160811 MGI PMID:22318315 1618349 Enho energy homeostasis associated gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:22318315 1618351 Kansl2 KAT8 regulatory NSL complex subunit 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20201002 MGI PMID:32541879 1618351 Kansl2 KAT8 regulatory NSL complex subunit 2 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20201002 MGI PMID:32541879 1618351 Kansl2 KAT8 regulatory NSL complex subunit 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20201002 MGI PMID:32541879 1618351 Kansl2 KAT8 regulatory NSL complex subunit 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20201002 MGI PMID:32541879 1618355 Mogat1 monoacylglycerol O-acyltransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170608 MGI PMID:26880786 1618355 Mogat1 monoacylglycerol O-acyltransferase 1 gene MP:0001426 polydipsia IAGP N RGD:5509061 20170608 MGI PMID:26880786 1618355 Mogat1 monoacylglycerol O-acyltransferase 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20171102 MGI PMID:26880786 1618355 Mogat1 monoacylglycerol O-acyltransferase 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20170608 MGI PMID:26880786 1618355 Mogat1 monoacylglycerol O-acyltransferase 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20170608 MGI PMID:26880786 1618355 Mogat1 monoacylglycerol O-acyltransferase 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20171102 MGI PMID:26880786 1618355 Mogat1 monoacylglycerol O-acyltransferase 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20170608 MGI PMID:26880786 1618355 Mogat1 monoacylglycerol O-acyltransferase 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20170608 MGI PMID:26880786 1618355 Mogat1 monoacylglycerol O-acyltransferase 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20170608 MGI PMID:26880786 1618355 Mogat1 monoacylglycerol O-acyltransferase 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20170608 MGI PMID:26880786 1618355 Mogat1 monoacylglycerol O-acyltransferase 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20170608 MGI PMID:26880786 1618355 Mogat1 monoacylglycerol O-acyltransferase 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20230119 MGI 1618357 Tmem174 transmembrane protein 174 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20220929 MGI PMID:35459732 1618357 Tmem174 transmembrane protein 174 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170105 MGI 1618357 Tmem174 transmembrane protein 174 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20220929 MGI PMID:35459732 1618357 Tmem174 transmembrane protein 174 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170105 MGI 1618357 Tmem174 transmembrane protein 174 gene MP:0002902 decreased urine phosphate level IAGP N RGD:5509061 20220929 MGI PMID:35459732 1618357 Tmem174 transmembrane protein 174 gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20220929 MGI PMID:35459732 1618357 Tmem174 transmembrane protein 174 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20170105 MGI 1618357 Tmem174 transmembrane protein 174 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20220929 MGI PMID:35459732 1618357 Tmem174 transmembrane protein 174 gene MP:0006133 calcified artery IAGP N RGD:5509061 20220929 MGI PMID:35459732 1618358 Ccdc88c coiled-coil domain containing 88C gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20231207 MGI 1618358 Ccdc88c coiled-coil domain containing 88C gene MP:0001147 small testis IEA N RGD:5509061 20231207 MGI 1618358 Ccdc88c coiled-coil domain containing 88C gene MP:0001263 weight loss IAGP N RGD:5509061 20201119 MGI PMID:22643886 1618358 Ccdc88c coiled-coil domain containing 88C gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20201119 MGI PMID:22643886 1618358 Ccdc88c coiled-coil domain containing 88C gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 1618358 Ccdc88c coiled-coil domain containing 88C gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20201022 MGI PMID:32535020 1618358 Ccdc88c coiled-coil domain containing 88C gene MP:0030963 abnormal brain ependyma motile cilium location or orientation IAGP N RGD:5509061 20201022 MGI PMID:32535020 1618360 Rab13 RAB13, member RAS oncogene family gene MP:0000692 small spleen IAGP N RGD:5509061 20230622 MGI PMID:25074980 1618360 Rab13 RAB13, member RAS oncogene family gene MP:0002223 lymphoid hypoplasia IAGP N RGD:5509061 20230622 MGI PMID:25074980 1618360 Rab13 RAB13, member RAS oncogene family gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20230622 MGI PMID:25074980 1618360 Rab13 RAB13, member RAS oncogene family gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20230622 MGI PMID:25074980 1618360 Rab13 RAB13, member RAS oncogene family gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20230622 MGI PMID:25074980 1618360 Rab13 RAB13, member RAS oncogene family gene MP:0009624 small inguinal lymph nodes IAGP N RGD:5509061 20230622 MGI PMID:25074980 1618360 Rab13 RAB13, member RAS oncogene family gene MP:0020212 impaired leukocyte migration IAGP N RGD:5509061 20230622 MGI PMID:25074980 1618360 Rab13 RAB13, member RAS oncogene family gene MP:0031207 decreased lymphocyte chemotaxis IAGP N RGD:5509061 20230622 MGI PMID:25074980 1618362 Aph1c aph1 homolog C, gamma secretase subunit gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160421 MGI 1618362 Aph1c aph1 homolog C, gamma secretase subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15665098 1618362 Aph1c aph1 homolog C, gamma secretase subunit gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1618362 Aph1c aph1 homolog C, gamma secretase subunit gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220519 MGI 1618363 Apoo apolipoprotein O gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20211021 MGI 1618366 Poglut3 protein O-glucosyltransferase 3 gene MP:0000564 syndactyly IAGP N RGD:5509061 20240801 MGI PMID:38844137 1618366 Poglut3 protein O-glucosyltransferase 3 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1618366 Poglut3 protein O-glucosyltransferase 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240801 MGI PMID:38844137 1618366 Poglut3 protein O-glucosyltransferase 3 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20240801 MGI PMID:38844137 1618366 Poglut3 protein O-glucosyltransferase 3 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1618366 Poglut3 protein O-glucosyltransferase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240801 MGI PMID:38844137 1618366 Poglut3 protein O-glucosyltransferase 3 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1618366 Poglut3 protein O-glucosyltransferase 3 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1618366 Poglut3 protein O-glucosyltransferase 3 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1618366 Poglut3 protein O-glucosyltransferase 3 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20240801 MGI PMID:38844137 1618366 Poglut3 protein O-glucosyltransferase 3 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1618366 Poglut3 protein O-glucosyltransferase 3 gene MP:0006083 abnormal blood vessel elastic tissue morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1618366 Poglut3 protein O-glucosyltransferase 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20240801 MGI PMID:38844137 1618366 Poglut3 protein O-glucosyltransferase 3 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20240801 MGI PMID:38844137 1618366 Poglut3 protein O-glucosyltransferase 3 gene MP:0031392 hypoactivity IAGP N RGD:5509061 20240801 MGI PMID:38844137 1618367 Trappc6a trafficking protein particle complex 6A gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20200310 MGI PMID:16697553 1618367 Trappc6a trafficking protein particle complex 6A gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20200310 MGI PMID:16697553 1618367 Trappc6a trafficking protein particle complex 6A gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20200310 MGI PMID:16697553 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0000601 small liver IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20231207 MGI 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20231207 MGI 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20231207 MGI 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20231207 MGI 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0001260 increased body weight IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0001297 microphthalmia IEA N RGD:5509061 20231207 MGI 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20231207 MGI 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0002871 albuminuria IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0002989 small kidney IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0011045 decreased lung elastance IEA N RGD:5509061 20240523 MGI 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0011891 decreased circulating ferritin level IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0011939 increased food intake IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618371 Ccdc198 coiled-coil domain containing 198 gene MP:0012298 hypoactivity in response to feed restriction IAGP N RGD:5509061 20240801 MGI PMID:37248239 1618372 1700019D03Rik RIKEN cDNA 1700019D03 gene gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1618372 1700019D03Rik RIKEN cDNA 1700019D03 gene gene MP:0005505 thrombocytosis IEA N RGD:5509061 20220519 MGI 1618372 1700019D03Rik RIKEN cDNA 1700019D03 gene gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 1618373 Catsperz cation channel sperm associated auxiliary subunit zeta gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1618373 Catsperz cation channel sperm associated auxiliary subunit zeta gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1618373 Catsperz cation channel sperm associated auxiliary subunit zeta gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1618373 Catsperz cation channel sperm associated auxiliary subunit zeta gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20170622 MGI PMID:28226241 1618373 Catsperz cation channel sperm associated auxiliary subunit zeta gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20170622 MGI PMID:28226241 1618373 Catsperz cation channel sperm associated auxiliary subunit zeta gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20201224 MGI PMID:31056283 1618373 Catsperz cation channel sperm associated auxiliary subunit zeta gene MP:0001925 male infertility IAGP N RGD:5509061 20170622 MGI PMID:28226241 1618373 Catsperz cation channel sperm associated auxiliary subunit zeta gene MP:0001935 decreased litter size IAGP N RGD:5509061 20170622 MGI PMID:28226241 1618373 Catsperz cation channel sperm associated auxiliary subunit zeta gene MP:0002546 mydriasis IEA N RGD:5509061 20220519 MGI 1618373 Catsperz cation channel sperm associated auxiliary subunit zeta gene MP:0002833 increased heart weight IEA N RGD:5509061 20220811 MGI 1618373 Catsperz cation channel sperm associated auxiliary subunit zeta gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20170622 MGI PMID:28226241 1618373 Catsperz cation channel sperm associated auxiliary subunit zeta gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20220714 MGI PMID:31056283 1618373 Catsperz cation channel sperm associated auxiliary subunit zeta gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1618373 Catsperz cation channel sperm associated auxiliary subunit zeta gene MP:0031011 abnormal sperm migration in female genital tract IAGP N RGD:5509061 20200227 MGI PMID:28226241 1618374 Romo1 reactive oxygen species modulator 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1618374 Romo1 reactive oxygen species modulator 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 1618374 Romo1 reactive oxygen species modulator 1 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20230601 MGI 1618374 Romo1 reactive oxygen species modulator 1 gene MP:0001722 pale yolk sac IEA N RGD:5509061 20230601 MGI 1618374 Romo1 reactive oxygen species modulator 1 gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20230601 MGI 1618374 Romo1 reactive oxygen species modulator 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 1618374 Romo1 reactive oxygen species modulator 1 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20230601 MGI 1618374 Romo1 reactive oxygen species modulator 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1618374 Romo1 reactive oxygen species modulator 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230601 MGI 1618374 Romo1 reactive oxygen species modulator 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20230601 MGI 1618378 Higd2a HIG1 domain family, member 2A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200310 MGI 1618378 Higd2a HIG1 domain family, member 2A gene MP:0000274 enlarged heart IEA N RGD:5509061 20200310 MGI 1618378 Higd2a HIG1 domain family, member 2A gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1618380 Fancl Fanconi anemia, complementation group L gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:1924340 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:12417526 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:1924340 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:8373945 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:12417526 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:1924340 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:8373945 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12417526 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:1924340 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:8373945 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12417526 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:1924340 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12417526 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:1924340 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8373945 1618380 Fancl Fanconi anemia, complementation group L gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:8373945 1618380 Fancl Fanconi anemia, complementation group L gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:1924340 1618380 Fancl Fanconi anemia, complementation group L gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160421 MGI 1618380 Fancl Fanconi anemia, complementation group L gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12417526 1618380 Fancl Fanconi anemia, complementation group L gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:1924340 1618380 Fancl Fanconi anemia, complementation group L gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1618380 Fancl Fanconi anemia, complementation group L gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:12417526 1618380 Fancl Fanconi anemia, complementation group L gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:1924340 1618380 Fancl Fanconi anemia, complementation group L gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:8373945 1618380 Fancl Fanconi anemia, complementation group L gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:1924340 1618380 Fancl Fanconi anemia, complementation group L gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:1924340 1618380 Fancl Fanconi anemia, complementation group L gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12417526 1618380 Fancl Fanconi anemia, complementation group L gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1618380 Fancl Fanconi anemia, complementation group L gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1618380 Fancl Fanconi anemia, complementation group L gene MP:0004806 absent germ cells IAGP N RGD:5509061 20141003 MGI PMID:12417526 1618380 Fancl Fanconi anemia, complementation group L gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12417526 1618380 Fancl Fanconi anemia, complementation group L gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:1924340 1618380 Fancl Fanconi anemia, complementation group L gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1618380 Fancl Fanconi anemia, complementation group L gene MP:0008257 thin myometrium IAGP N RGD:5509061 20141003 MGI PMID:1924340 1618380 Fancl Fanconi anemia, complementation group L gene MP:0008257 thin myometrium IAGP N RGD:5509061 20141003 MGI PMID:8373945 1618380 Fancl Fanconi anemia, complementation group L gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12417526 1618380 Fancl Fanconi anemia, complementation group L gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:1924340 1618380 Fancl Fanconi anemia, complementation group L gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:8373945 1618380 Fancl Fanconi anemia, complementation group L gene MP:0009094 abnormal endometrial gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8373945 1618380 Fancl Fanconi anemia, complementation group L gene MP:0009226 small uterine cervix IAGP N RGD:5509061 20141003 MGI PMID:1924340 1618380 Fancl Fanconi anemia, complementation group L gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:12417526 1618380 Fancl Fanconi anemia, complementation group L gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1618380 Fancl Fanconi anemia, complementation group L gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1618380 Fancl Fanconi anemia, complementation group L gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12417526 1618380 Fancl Fanconi anemia, complementation group L gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12417526 1618380 Fancl Fanconi anemia, complementation group L gene MP:0030934 decreased primordial germ cell proliferation IAGP N RGD:5509061 20190411 MGI PMID:12417526 1618380 Fancl Fanconi anemia, complementation group L gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:8373945 1618380 Fancl Fanconi anemia, complementation group L gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220804 MGI PMID:8373945 1618381 Tmem88 transmembrane protein 88 gene MP:0002764 short tibia IEA N RGD:5509061 20240523 MGI 1618385 Fancg Fanconi anemia, complementation group G gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:11719385 1618385 Fancg Fanconi anemia, complementation group G gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:11823446 1618385 Fancg Fanconi anemia, complementation group G gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:11823446 1618385 Fancg Fanconi anemia, complementation group G gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11719385 1618385 Fancg Fanconi anemia, complementation group G gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11823446 1618385 Fancg Fanconi anemia, complementation group G gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:11719385 1618385 Fancg Fanconi anemia, complementation group G gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11823446 1618385 Fancg Fanconi anemia, complementation group G gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:11823446 1618385 Fancg Fanconi anemia, complementation group G gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11719385 1618385 Fancg Fanconi anemia, complementation group G gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11823446 1618385 Fancg Fanconi anemia, complementation group G gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11719385 1618385 Fancg Fanconi anemia, complementation group G gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11823446 1618385 Fancg Fanconi anemia, complementation group G gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:11719385 1618385 Fancg Fanconi anemia, complementation group G gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11823446 1618385 Fancg Fanconi anemia, complementation group G gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11719385 1618385 Fancg Fanconi anemia, complementation group G gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11823446 1618385 Fancg Fanconi anemia, complementation group G gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:11719385 1618385 Fancg Fanconi anemia, complementation group G gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:11823446 1618385 Fancg Fanconi anemia, complementation group G gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:11719385 1618385 Fancg Fanconi anemia, complementation group G gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:11823446 1618385 Fancg Fanconi anemia, complementation group G gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:11823446 1618385 Fancg Fanconi anemia, complementation group G gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11719385 1618386 Acss2 acyl-CoA synthetase short-chain family member 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20240502 MGI PMID:38515158 1618386 Acss2 acyl-CoA synthetase short-chain family member 2 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20240502 MGI PMID:38515158 1618386 Acss2 acyl-CoA synthetase short-chain family member 2 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20240502 MGI PMID:38515158 1618386 Acss2 acyl-CoA synthetase short-chain family member 2 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20240502 MGI PMID:38515158 1618386 Acss2 acyl-CoA synthetase short-chain family member 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20240502 MGI PMID:38515158 1618386 Acss2 acyl-CoA synthetase short-chain family member 2 gene MP:0014364 decreased pyroptosis IAGP N RGD:5509061 20240502 MGI PMID:38515158 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20160623 MGI PMID:19856415 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20160623 MGI PMID:19856415 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0001293 anophthalmia IEA N RGD:5509061 20181227 MGI 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20160623 MGI PMID:19856415 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20531296 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20160623 MGI PMID:26035389 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20160623 MGI PMID:19856415 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0005000 abnormal immune tolerance IAGP N RGD:5509061 20160623 MGI PMID:26035389 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0005036 diarrhea IAGP N RGD:5509061 20160623 MGI PMID:19856415 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20160623 MGI PMID:26035389 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20160623 MGI PMID:26035389 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0008528 polycystic kidney IEA N RGD:5509061 20181227 MGI 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20160623 MGI PMID:19856415 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20160623 MGI PMID:26035389 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20160623 MGI PMID:26035389 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20160623 MGI PMID:19856415 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0014201 abnormal intestinal epithelium physiology IAGP N RGD:5509061 20160623 MGI PMID:19856415 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0014201 abnormal intestinal epithelium physiology IAGP N RGD:5509061 20160623 MGI PMID:26035389 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0014219 decreased intestinal mucosa thickness IAGP N RGD:5509061 20160623 MGI PMID:19856415 1618387 Gpa33 glycoprotein A33 transmembrane gene MP:0014222 decreased colon goblet cell number IAGP N RGD:5509061 20160623 MGI PMID:19856415 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15240667 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11371359 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11371359 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15630136 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0002345 abnormal lymph node primary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0002345 abnormal lymph node primary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:15630136 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:15630136 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:16973390 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11371359 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11371359 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15240667 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11371359 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:11371359 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0008471 abnormal spleen primary B follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15630136 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11429549 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:12594954 1618388 Tnfrsf13b tumor necrosis factor receptor superfamily, member 13b gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:12594954 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:15263024 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:16172260 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:16172260 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:14993294 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210520 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20200310 MGI PMID:15263024 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20200310 MGI PMID:22585305 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:16172260 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20221215 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0002816 colitis IAGP N RGD:5509061 20200310 MGI PMID:21820333 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200310 MGI PMID:16172260 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:14993294 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:15263024 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:16172260 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:15263024 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:16172260 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:21820333 1618389 Crlf2 cytokine receptor-like factor 2 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1618390 Gsdma gasdermin A gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20220721 MGI PMID:35110732 1618390 Gsdma gasdermin A gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20220721 MGI PMID:35110732 1618392 Pnkd paroxysmal nonkinesiogenic dyskinesia gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22214848 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:20493731 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20141003 MGI PMID:20493731 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20493731 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008556 abnormal tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008654 increased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008691 decreased interleukin-23 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20493731 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0009787 increased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20493731 1618394 Clec4n C-type lectin domain family 4, member n gene MP:0020183 abnormal susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:24343653 1618396 Vps25 vacuolar protein sorting 25 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0000445 short snout IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0000547 short limbs IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0000562 polydactyly IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1618396 Vps25 vacuolar protein sorting 25 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20240523 MGI 1618396 Vps25 vacuolar protein sorting 25 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 1618396 Vps25 vacuolar protein sorting 25 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0004342 scapular bone foramen IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1618396 Vps25 vacuolar protein sorting 25 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20160324 MGI PMID:25373905 1618396 Vps25 vacuolar protein sorting 25 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1618396 Vps25 vacuolar protein sorting 25 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1618396 Vps25 vacuolar protein sorting 25 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1618397 Selenoi selenoprotein I gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20210513 MGI PMID:32502470 1618397 Selenoi selenoprotein I gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20210513 MGI PMID:32502470 1618398 Larp7 La ribonucleoprotein 7, transcriptional regulator gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:23154982 1618398 Larp7 La ribonucleoprotein 7, transcriptional regulator gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:23154982 1618398 Larp7 La ribonucleoprotein 7, transcriptional regulator gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:23154982 1618398 Larp7 La ribonucleoprotein 7, transcriptional regulator gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23154982 1618398 Larp7 La ribonucleoprotein 7, transcriptional regulator gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23154982 1618398 Larp7 La ribonucleoprotein 7, transcriptional regulator gene MP:0030934 decreased primordial germ cell proliferation IAGP N RGD:5509061 20190411 MGI PMID:23154982 1618400 Washc2 WASH complex subunit 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1618400 Washc2 WASH complex subunit 2 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1618400 Washc2 WASH complex subunit 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1618400 Washc2 WASH complex subunit 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1618401 Vmn1r49 vomeronasal 1, receptor 49 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17942483 1618401 Vmn1r49 vomeronasal 1, receptor 49 gene MP:0009945 abnormal accessory olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:10219241 1618401 Vmn1r49 vomeronasal 1, receptor 49 gene MP:0009945 abnormal accessory olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17942483 1618401 Vmn1r49 vomeronasal 1, receptor 49 gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:10219241 1618405 Ccl1 C-C motif chemokine ligand 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18714025 1618405 Ccl1 C-C motif chemokine ligand 1 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18714025 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0001391 abnormal tail movements IAGP N RGD:5509061 20141003 MGI PMID:17567668 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:17567668 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10477299 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:10477299 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:10477299 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10477299 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10477299 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:17567668 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17567668 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:10477299 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0003097 abnormal tendon stiffness IAGP N RGD:5509061 20141003 MGI PMID:17567668 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10477299 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:10477299 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:17567668 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:10477299 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:17567668 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:10477299 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:10477299 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10477299 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10477299 1618406 Scx scleraxis scleraxis bHLH transcription factor gene MP:0011187 abnormal parietal endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10477299 1618407 Zc3h7b zinc finger CCCH type containing 7B gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1618407 Zc3h7b zinc finger CCCH type containing 7B gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20230601 MGI 1618411 Acsm3 acyl-CoA synthetase medium-chain family member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:12707288 1618420 Cep250 centrosomal protein 250 gene MP:0001147 small testis IAGP N RGD:5509061 20220811 MGI PMID:35127699 1618420 Cep250 centrosomal protein 250 gene MP:0001147 small testis IAGP N RGD:5509061 20230330 MGI PMID:35599622 1618420 Cep250 centrosomal protein 250 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20230330 MGI PMID:35599622 1618420 Cep250 centrosomal protein 250 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20190912 MGI PMID:30998843 1618420 Cep250 centrosomal protein 250 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20230330 MGI PMID:35599622 1618420 Cep250 centrosomal protein 250 gene MP:0001925 male infertility IAGP N RGD:5509061 20220811 MGI PMID:35127699 1618420 Cep250 centrosomal protein 250 gene MP:0001925 male infertility IAGP N RGD:5509061 20230330 MGI PMID:35599622 1618420 Cep250 centrosomal protein 250 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20230330 MGI PMID:35599622 1618420 Cep250 centrosomal protein 250 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20190912 MGI PMID:30998843 1618420 Cep250 centrosomal protein 250 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1618420 Cep250 centrosomal protein 250 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20230330 MGI PMID:35599622 1618420 Cep250 centrosomal protein 250 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20230330 MGI PMID:35599622 1618420 Cep250 centrosomal protein 250 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220811 MGI PMID:35127699 1618420 Cep250 centrosomal protein 250 gene MP:0005159 azoospermia IAGP N RGD:5509061 20230330 MGI PMID:35599622 1618420 Cep250 centrosomal protein 250 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20230330 MGI PMID:35599622 1618420 Cep250 centrosomal protein 250 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20230330 MGI PMID:35599622 1618420 Cep250 centrosomal protein 250 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20181227 MGI 1618420 Cep250 centrosomal protein 250 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20220811 MGI PMID:35127699 1618420 Cep250 centrosomal protein 250 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20190912 MGI PMID:30998843 1618420 Cep250 centrosomal protein 250 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20190912 MGI PMID:30998843 1618420 Cep250 centrosomal protein 250 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1618420 Cep250 centrosomal protein 250 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20190912 MGI PMID:30998843 1618420 Cep250 centrosomal protein 250 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20190912 MGI PMID:30998843 1618420 Cep250 centrosomal protein 250 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20190912 MGI PMID:30998843 1618420 Cep250 centrosomal protein 250 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20190912 MGI PMID:30998843 1618420 Cep250 centrosomal protein 250 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20190912 MGI PMID:30998843 1618420 Cep250 centrosomal protein 250 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220811 MGI PMID:35127699 1618420 Cep250 centrosomal protein 250 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20220811 MGI PMID:35127699 1618420 Cep250 centrosomal protein 250 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20230330 MGI PMID:35599622 1618426 H2-T18 histocompatibility 2, T region locus 18 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19004778 1618426 H2-T18 histocompatibility 2, T region locus 18 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:19004778 1618426 H2-T18 histocompatibility 2, T region locus 18 gene MP:0008361 abnormal CD8-positive, gamma-delta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19004778 1618426 H2-T18 histocompatibility 2, T region locus 18 gene MP:0008401 abnormal CD8 positive, alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19004778 1618426 H2-T18 histocompatibility 2, T region locus 18 gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19004778 1618426 H2-T18 histocompatibility 2, T region locus 18 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19004778 1618426 H2-T18 histocompatibility 2, T region locus 18 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19004778 1618426 H2-T18 histocompatibility 2, T region locus 18 gene MP:0008894 abnormal intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19004778 1618426 H2-T18 histocompatibility 2, T region locus 18 gene MP:0008895 abnormal intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:19004778 1618434 En1 engrailed 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20210902 MGI PMID:33568816 1618434 En1 engrailed 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21093436 1618434 En1 engrailed 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15121182 1618434 En1 engrailed 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:9362463 1618434 En1 engrailed 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:12832534 1618434 En1 engrailed 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20210902 MGI PMID:33568816 1618434 En1 engrailed 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:12832534 1618434 En1 engrailed 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20210902 MGI PMID:33568816 1618434 En1 engrailed 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:9362463 1618434 En1 engrailed 1 gene MP:0000567 truncated digits IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0000568 ectopic digits IAGP N RGD:5509061 20141003 MGI PMID:8684466 1618434 En1 engrailed 1 gene MP:0000569 abnormal digit pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12832534 1618434 En1 engrailed 1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:8684466 1618434 En1 engrailed 1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:9362463 1618434 En1 engrailed 1 gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20141003 MGI PMID:8684466 1618434 En1 engrailed 1 gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20141003 MGI PMID:9362463 1618434 En1 engrailed 1 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:8684466 1618434 En1 engrailed 1 gene MP:0000580 deformed nails IAGP N RGD:5509061 20141003 MGI PMID:12832534 1618434 En1 engrailed 1 gene MP:0000580 deformed nails IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0000675 abnormal eccrine sweat gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8684466 1618434 En1 engrailed 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23152632 1618434 En1 engrailed 1 gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0000777 increased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:10490025 1618434 En1 engrailed 1 gene MP:0000777 increased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:12367504 1618434 En1 engrailed 1 gene MP:0000777 increased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:15121182 1618434 En1 engrailed 1 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0000836 abnormal substantia nigra morphology IAGP N RGD:5509061 20141003 MGI PMID:19968985 1618434 En1 engrailed 1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15121182 1618434 En1 engrailed 1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:18480159 1618434 En1 engrailed 1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:23444360 1618434 En1 engrailed 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10490025 1618434 En1 engrailed 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12682014 1618434 En1 engrailed 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:15121182 1618434 En1 engrailed 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:18480159 1618434 En1 engrailed 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20210715 MGI PMID:33899734 1618434 En1 engrailed 1 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:12832534 1618434 En1 engrailed 1 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20210715 MGI PMID:33899734 1618434 En1 engrailed 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17664423 1618434 En1 engrailed 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17693261 1618434 En1 engrailed 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:18480159 1618434 En1 engrailed 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19752021 1618434 En1 engrailed 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19968985 1618434 En1 engrailed 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20210715 MGI PMID:33899734 1618434 En1 engrailed 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:12367504 1618434 En1 engrailed 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:15207855 1618434 En1 engrailed 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:16884697 1618434 En1 engrailed 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:19752021 1618434 En1 engrailed 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:12367504 1618434 En1 engrailed 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:18480159 1618434 En1 engrailed 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20210715 MGI PMID:33899734 1618434 En1 engrailed 1 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:10490025 1618434 En1 engrailed 1 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0000865 absent cerebellum vermis IAGP N RGD:5509061 20141003 MGI PMID:12682014 1618434 En1 engrailed 1 gene MP:0000865 absent cerebellum vermis IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12367504 1618434 En1 engrailed 1 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0000867 abnormal cerebellum anterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0000867 abnormal cerebellum anterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0000868 decreased anterior vermis size IAGP N RGD:5509061 20141003 MGI PMID:10490025 1618434 En1 engrailed 1 gene MP:0000868 decreased anterior vermis size IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0000868 decreased anterior vermis size IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0000869 abnormal cerebellum posterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0000869 abnormal cerebellum posterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20210715 MGI PMID:33899734 1618434 En1 engrailed 1 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:18480159 1618434 En1 engrailed 1 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:19752021 1618434 En1 engrailed 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17693261 1618434 En1 engrailed 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:23152632 1618434 En1 engrailed 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20180927 MGI PMID:29769718 1618434 En1 engrailed 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:17664423 1618434 En1 engrailed 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:19752021 1618434 En1 engrailed 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20210715 MGI PMID:33899734 1618434 En1 engrailed 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:12682014 1618434 En1 engrailed 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:19968985 1618434 En1 engrailed 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:23444360 1618434 En1 engrailed 1 gene MP:0000899 abnormal corpora quadrigemina morphology IAGP N RGD:5509061 20141003 MGI PMID:10490025 1618434 En1 engrailed 1 gene MP:0000905 increased superior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:10490025 1618434 En1 engrailed 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:18344997 1618434 En1 engrailed 1 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:18480159 1618434 En1 engrailed 1 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:19968985 1618434 En1 engrailed 1 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:23444360 1618434 En1 engrailed 1 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0001062 absent oculomotor nerve IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0001063 abnormal trochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12682014 1618434 En1 engrailed 1 gene MP:0001064 absent trochlear nerve IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141218 MGI PMID:24937429 1618434 En1 engrailed 1 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12367504 1618434 En1 engrailed 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141218 MGI PMID:24937429 1618434 En1 engrailed 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23152632 1618434 En1 engrailed 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12832534 1618434 En1 engrailed 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17693261 1618434 En1 engrailed 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19679071 1618434 En1 engrailed 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:23152632 1618434 En1 engrailed 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10490025 1618434 En1 engrailed 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:23152632 1618434 En1 engrailed 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22745501 1618434 En1 engrailed 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17015829 1618434 En1 engrailed 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10490025 1618434 En1 engrailed 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12682014 1618434 En1 engrailed 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16525473 1618434 En1 engrailed 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141218 MGI PMID:24937429 1618434 En1 engrailed 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10490025 1618434 En1 engrailed 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12682014 1618434 En1 engrailed 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23152632 1618434 En1 engrailed 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:12682014 1618434 En1 engrailed 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141218 MGI PMID:24937429 1618434 En1 engrailed 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:17693261 1618434 En1 engrailed 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:17693261 1618434 En1 engrailed 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:19479951 1618434 En1 engrailed 1 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:8684466 1618434 En1 engrailed 1 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:9362463 1618434 En1 engrailed 1 gene MP:0001679 thin apical ectodermal ridge IAGP N RGD:5509061 20150521 MGI PMID:8684466 1618434 En1 engrailed 1 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:12367504 1618434 En1 engrailed 1 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22745501 1618434 En1 engrailed 1 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:12764108 1618434 En1 engrailed 1 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22745501 1618434 En1 engrailed 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9362463 1618434 En1 engrailed 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19679071 1618434 En1 engrailed 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23152632 1618434 En1 engrailed 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9362463 1618434 En1 engrailed 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:10477289 1618434 En1 engrailed 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:8684466 1618434 En1 engrailed 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20210902 MGI PMID:33568816 1618434 En1 engrailed 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:12832534 1618434 En1 engrailed 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:8684466 1618434 En1 engrailed 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9362463 1618434 En1 engrailed 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8684466 1618434 En1 engrailed 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19968985 1618434 En1 engrailed 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10490025 1618434 En1 engrailed 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:23152632 1618434 En1 engrailed 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9362463 1618434 En1 engrailed 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17664423 1618434 En1 engrailed 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18344997 1618434 En1 engrailed 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7624797 1618434 En1 engrailed 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20141218 MGI PMID:24937429 1618434 En1 engrailed 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:10477289 1618434 En1 engrailed 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:23444360 1618434 En1 engrailed 1 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:10490025 1618434 En1 engrailed 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:16525473 1618434 En1 engrailed 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141127 MGI PMID:25281317 1618434 En1 engrailed 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141218 MGI PMID:24937429 1618434 En1 engrailed 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22745501 1618434 En1 engrailed 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:22745501 1618434 En1 engrailed 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12764108 1618434 En1 engrailed 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23152632 1618434 En1 engrailed 1 gene MP:0002892 decreased superior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0002892 decreased superior colliculus size IAGP N RGD:5509061 20210715 MGI PMID:33899734 1618434 En1 engrailed 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:10477289 1618434 En1 engrailed 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15121182 1618434 En1 engrailed 1 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:15207855 1618434 En1 engrailed 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17693261 1618434 En1 engrailed 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20210715 MGI PMID:33899734 1618434 En1 engrailed 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:21093436 1618434 En1 engrailed 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:23152632 1618434 En1 engrailed 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20180927 MGI PMID:29769718 1618434 En1 engrailed 1 gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20141127 MGI PMID:25281317 1618434 En1 engrailed 1 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21093436 1618434 En1 engrailed 1 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:17015829 1618434 En1 engrailed 1 gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19088086 1618434 En1 engrailed 1 gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20210715 MGI PMID:33899734 1618434 En1 engrailed 1 gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20210715 MGI PMID:33899734 1618434 En1 engrailed 1 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:10490025 1618434 En1 engrailed 1 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21093436 1618434 En1 engrailed 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23152632 1618434 En1 engrailed 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:10477289 1618434 En1 engrailed 1 gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20141003 MGI PMID:12682014 1618434 En1 engrailed 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:8684466 1618434 En1 engrailed 1 gene MP:0003813 abnormal hair follicle dermal papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:8684466 1618434 En1 engrailed 1 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:12367504 1618434 En1 engrailed 1 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0003877 abnormal serotonergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12764108 1618434 En1 engrailed 1 gene MP:0003877 abnormal serotonergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19088086 1618434 En1 engrailed 1 gene MP:0003877 abnormal serotonergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19968985 1618434 En1 engrailed 1 gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:17015829 1618434 En1 engrailed 1 gene MP:0004096 abnormal midbrain-hindbrain boundary development IAGP N RGD:5509061 20141003 MGI PMID:11124114 1618434 En1 engrailed 1 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20210715 MGI PMID:33899734 1618434 En1 engrailed 1 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0004321 short sternum IAGP N RGD:5509061 20210902 MGI PMID:33568816 1618434 En1 engrailed 1 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0004861 abnormal Raphe nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19968985 1618434 En1 engrailed 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17015829 1618434 En1 engrailed 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15207855 1618434 En1 engrailed 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:23444360 1618434 En1 engrailed 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20210715 MGI PMID:33899734 1618434 En1 engrailed 1 gene MP:0005323 dystonia IAGP N RGD:5509061 20141218 MGI PMID:24937429 1618434 En1 engrailed 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19679071 1618434 En1 engrailed 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141127 MGI PMID:25281317 1618434 En1 engrailed 1 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:17015829 1618434 En1 engrailed 1 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:23152632 1618434 En1 engrailed 1 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141127 MGI PMID:25281317 1618434 En1 engrailed 1 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:10490025 1618434 En1 engrailed 1 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:12832534 1618434 En1 engrailed 1 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:16571625 1618434 En1 engrailed 1 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0006098 absent cerebellar lobules IAGP N RGD:5509061 20141003 MGI PMID:10490025 1618434 En1 engrailed 1 gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20141003 MGI PMID:18480159 1618434 En1 engrailed 1 gene MP:0006105 small tectum IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0006106 absent tectum IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:19479951 1618434 En1 engrailed 1 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141127 MGI PMID:25281317 1618434 En1 engrailed 1 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17015829 1618434 En1 engrailed 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:17693261 1618434 En1 engrailed 1 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:8684466 1618434 En1 engrailed 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:23152632 1618434 En1 engrailed 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21093436 1618434 En1 engrailed 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22745501 1618434 En1 engrailed 1 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22745501 1618434 En1 engrailed 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:21093436 1618434 En1 engrailed 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21093436 1618434 En1 engrailed 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23444360 1618434 En1 engrailed 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141218 MGI PMID:24937429 1618434 En1 engrailed 1 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:12832534 1618434 En1 engrailed 1 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20210715 MGI PMID:33899734 1618434 En1 engrailed 1 gene MP:0009039 absent inferior colliculus IAGP N RGD:5509061 20141003 MGI PMID:12682014 1618434 En1 engrailed 1 gene MP:0009039 absent inferior colliculus IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0009040 absent superior colliculus IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0009041 absent colliculi IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0009048 enlarged tectum IAGP N RGD:5509061 20141003 MGI PMID:18480159 1618434 En1 engrailed 1 gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:14762144 1618434 En1 engrailed 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:19752021 1618434 En1 engrailed 1 gene MP:0009718 absent Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:17664423 1618434 En1 engrailed 1 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:19752021 1618434 En1 engrailed 1 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22745501 1618434 En1 engrailed 1 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:22745501 1618434 En1 engrailed 1 gene MP:0009779 enhanced behavioral response to anesthetic IAGP N RGD:5509061 20141003 MGI PMID:22745501 1618434 En1 engrailed 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:10477289 1618434 En1 engrailed 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19088086 1618434 En1 engrailed 1 gene MP:0009957 abnormal cerebellum vermis lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0009963 abnormal cerebellum hemisphere lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0009968 abnormal cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20141127 MGI PMID:25281317 1618434 En1 engrailed 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:17015829 1618434 En1 engrailed 1 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:12764108 1618434 En1 engrailed 1 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20141127 MGI PMID:25281317 1618434 En1 engrailed 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17693261 1618434 En1 engrailed 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19752021 1618434 En1 engrailed 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12367504 1618434 En1 engrailed 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12832534 1618434 En1 engrailed 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15121182 1618434 En1 engrailed 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15207855 1618434 En1 engrailed 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7925010 1618434 En1 engrailed 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17015829 1618434 En1 engrailed 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19968985 1618434 En1 engrailed 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20081196 1618434 En1 engrailed 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14762144 1618434 En1 engrailed 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9362463 1618434 En1 engrailed 1 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:17015829 1618434 En1 engrailed 1 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:19968985 1618434 En1 engrailed 1 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141127 MGI PMID:25281317 1618434 En1 engrailed 1 gene MP:0011450 ectopic dopaminergic neuron IAGP N RGD:5509061 20141003 MGI PMID:12764108 1618434 En1 engrailed 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:17015829 1618434 En1 engrailed 1 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:11124114 1618434 En1 engrailed 1 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:10477289 1618434 En1 engrailed 1 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:23444360 1618434 En1 engrailed 1 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:9778510 1618434 En1 engrailed 1 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:12367504 1618434 En1 engrailed 1 gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20141003 MGI PMID:11124114 1618434 En1 engrailed 1 gene MP:0012267 abnormal red nucleus morphology IAGP N RGD:5509061 20141218 MGI PMID:24937429 1618434 En1 engrailed 1 gene MP:0012281 decreased sternebra size IAGP N RGD:5509061 20210902 MGI PMID:33568816 1618434 En1 engrailed 1 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:12367504 1618434 En1 engrailed 1 gene MP:0012706 decreased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12367504 1618434 En1 engrailed 1 gene MP:0012785 decreased rhombomere 1 size IAGP N RGD:5509061 20141003 MGI PMID:11124114 1618434 En1 engrailed 1 gene MP:0012785 decreased rhombomere 1 size IAGP N RGD:5509061 20141003 MGI PMID:17537797 1618434 En1 engrailed 1 gene MP:0012785 decreased rhombomere 1 size IAGP N RGD:5509061 20141003 MGI PMID:23444360 1618434 En1 engrailed 1 gene MP:0012787 absent rhombomere 1 IAGP N RGD:5509061 20141003 MGI PMID:11124114 1618434 En1 engrailed 1 gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20141003 MGI PMID:23152632 1618434 En1 engrailed 1 gene MP:0014331 abnormal Purkinje cell mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:19752021 1618434 En1 engrailed 1 gene MP:0014345 abnormal neuron mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:17693261 1618434 En1 engrailed 1 gene MP:0020393 increased neuronal precursor proliferation IAGP N RGD:5509061 20210715 MGI PMID:33899734 1618434 En1 engrailed 1 gene MP:0021103 abnormal ventral interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:16525473 1618434 En1 engrailed 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:12764108 1618434 En1 engrailed 1 gene MP:0031442 enlarged cerebral aqueduct IAGP N RGD:5509061 20221103 MGI PMID:18480159 1618435 Ms4a1 membrane-spanning 4-domains, subfamily A, member 1 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20200310 MGI PMID:14688067 1618435 Ms4a1 membrane-spanning 4-domains, subfamily A, member 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20200310 MGI PMID:14688067 1618435 Ms4a1 membrane-spanning 4-domains, subfamily A, member 1 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20200310 MGI PMID:14688067 1618435 Ms4a1 membrane-spanning 4-domains, subfamily A, member 1 gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20200310 MGI PMID:14688067 1618435 Ms4a1 membrane-spanning 4-domains, subfamily A, member 1 gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:14688067 1618437 Cct6b chaperonin containing TCP1 subunit 6B gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210805 MGI PMID:34141486 1618437 Cct6b chaperonin containing TCP1 subunit 6B gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20210805 MGI PMID:34141486 1618437 Cct6b chaperonin containing TCP1 subunit 6B gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210805 MGI PMID:34141486 1618439 Noct nocturnin gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20200310 MGI PMID:17517647 1618439 Noct nocturnin gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200310 MGI PMID:17517647 1618439 Noct nocturnin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:17517647 1618439 Noct nocturnin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:17517647 1618439 Noct nocturnin gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:17517647 1618441 Cbr2 carbonyl reductase 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20210520 MGI 1618441 Cbr2 carbonyl reductase 2 gene MP:0001304 cataract IEA N RGD:5509061 20210520 MGI 1618441 Cbr2 carbonyl reductase 2 gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20181227 MGI 1618441 Cbr2 carbonyl reductase 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1618443 Vmn2r65 vomeronasal 2, receptor 65 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20190711 MGI PMID:30550786 1618443 Vmn2r65 vomeronasal 2, receptor 65 gene MP:0021118 abnormal paternal behavior IAGP N RGD:5509061 20220519 MGI PMID:30550786 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20150205 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20150205 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20141003 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:16982049 1618444 Zglp1 zinc finger, GATA-like protein 1 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20150312 MGI PMID:16982049 1618449 Stard9 StAR related lipid transfer domain containing 9 gene MP:0000745 tremors IAGP N RGD:5509061 20231109 MGI PMID:36861884 1618449 Stard9 StAR related lipid transfer domain containing 9 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20231109 MGI PMID:36861884 1618449 Stard9 StAR related lipid transfer domain containing 9 gene MP:0001393 ataxia IAGP N RGD:5509061 20231109 MGI PMID:36861884 1618449 Stard9 StAR related lipid transfer domain containing 9 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20231109 MGI PMID:36861884 1618449 Stard9 StAR related lipid transfer domain containing 9 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1618449 Stard9 StAR related lipid transfer domain containing 9 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1618449 Stard9 StAR related lipid transfer domain containing 9 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20231109 MGI PMID:36861884 1618626 Ctag2l2 CTAG2 like 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200402 MGI 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:23185619 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20818428 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0001258 decreased body length IEA N RGD:5509061 20160804 MGI 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20357757 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20357757 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0001406 abnormal gait IEA N RGD:5509061 20160804 MGI 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20220421 MGI PMID:20357757 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20211021 MGI 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:20357757 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:20357757 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0001925 male infertility IAGP N RGD:5509061 20201015 MGI PMID:25568307 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15791206 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20201015 MGI PMID:25568307 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20201015 MGI PMID:25568307 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:20357757 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:17908561 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0003064 decreased coping response IAGP N RGD:5509061 20141003 MGI PMID:20357757 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:22623685 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20160804 MGI 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17908561 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20160804 MGI 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17908561 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21035757 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17908561 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160804 MGI 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20357757 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20201015 MGI PMID:25568307 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20210819 MGI PMID:20357757 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20210819 MGI PMID:20357757 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20357757 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20201015 MGI PMID:25568307 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20160804 MGI 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20210128 MGI 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:17908561 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:15791206 1618666 Gsk3a glycogen synthase kinase 3 alpha gene MP:0030431 wide metopic suture IAGP N RGD:5509061 20171214 MGI PMID:23185619 1618673 Klhdc7b kelch domain containing 7B gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210128 MGI 1618673 Klhdc7b kelch domain containing 7B gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20201022 MGI 1618673 Klhdc7b kelch domain containing 7B gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20201022 MGI 1618673 Klhdc7b kelch domain containing 7B gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20201022 MGI 1618673 Klhdc7b kelch domain containing 7B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1618673 Klhdc7b kelch domain containing 7B gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1618673 Klhdc7b kelch domain containing 7B gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1618673 Klhdc7b kelch domain containing 7B gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20201022 MGI 1618684 Sh2d1b2 SH2 domain containing 1B2 gene MP:0003080 increased natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:16127454 1618684 Sh2d1b2 SH2 domain containing 1B2 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:19151721 1618684 Sh2d1b2 SH2 domain containing 1B2 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:20962259 1618684 Sh2d1b2 SH2 domain containing 1B2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20962259 1618686 Hmcn1 hemicentin 1 gene MP:0001304 cataract IEA N RGD:5509061 20200310 MGI 1618686 Hmcn1 hemicentin 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1618686 Hmcn1 hemicentin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210429 MGI PMID:32035013 1618686 Hmcn1 hemicentin 1 gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20210617 MGI PMID:21215633 1618686 Hmcn1 hemicentin 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20201231 MGI 1618686 Hmcn1 hemicentin 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20210617 MGI PMID:21215633 1618708 Usp51 ubiquitin specific protease 51 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 1618713 Maml3 mastermind like transcriptional coactivator 3 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:22069191 1618713 Maml3 mastermind like transcriptional coactivator 3 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:22069191 1618713 Maml3 mastermind like transcriptional coactivator 3 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:22069191 1618713 Maml3 mastermind like transcriptional coactivator 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22069191 1618713 Maml3 mastermind like transcriptional coactivator 3 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:22069191 1618713 Maml3 mastermind like transcriptional coactivator 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22069191 1618713 Maml3 mastermind like transcriptional coactivator 3 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:22069191 1618713 Maml3 mastermind like transcriptional coactivator 3 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:22069191 1618713 Maml3 mastermind like transcriptional coactivator 3 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:22069191 1618713 Maml3 mastermind like transcriptional coactivator 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22069191 1618721 Actmap actin maturation protease gene MP:0000747 muscle weakness IAGP N RGD:5509061 20230119 MGI PMID:36173861 1618721 Actmap actin maturation protease gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20230119 MGI PMID:36173861 1618721 Actmap actin maturation protease gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20230119 MGI PMID:36173861 1618721 Actmap actin maturation protease gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20230119 MGI PMID:36173861 1618721 Actmap actin maturation protease gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20230119 MGI PMID:36173861 1618721 Actmap actin maturation protease gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20230119 MGI PMID:36173861 1618724 Krt74 keratin 74 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1618725 Krt40 keratin 40 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1618726 Krt77 keratin 77 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220811 MGI 1618727 Krt87 keratin 87 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20240523 MGI 1618729 Dbpht2 DNA binding protein with his-thr domain gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20240523 MGI 1618741 Zfp488 zinc finger protein 488 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1618746 L1td1 LINE-1 type transposase domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21637830 1618748 Tmem240 transmembrane protein 240 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20200514 MGI 1618748 Tmem240 transmembrane protein 240 gene MP:0000745 tremors IEA N RGD:5509061 20221215 MGI 1618748 Tmem240 transmembrane protein 240 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200514 MGI 1618748 Tmem240 transmembrane protein 240 gene MP:0001147 small testis IEA N RGD:5509061 20200514 MGI 1618748 Tmem240 transmembrane protein 240 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210128 MGI 1618748 Tmem240 transmembrane protein 240 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20200514 MGI 1618748 Tmem240 transmembrane protein 240 gene MP:0001399 hyperactivity IEA N RGD:5509061 20200514 MGI 1618748 Tmem240 transmembrane protein 240 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20201022 MGI 1618748 Tmem240 transmembrane protein 240 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1618748 Tmem240 transmembrane protein 240 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200514 MGI 1618748 Tmem240 transmembrane protein 240 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1618756 Mroh7 maestro heat-like repeat family member 7 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38697008 1618757 Ube2u ubiquitin-conjugating enzyme E2U (putative) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1618760 Mexis macrophage expressed LXRa(NR1H3)-dependent amplifier of Abca1 transcription lncRNA gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200423 MGI PMID:29431742 1618760 Mexis macrophage expressed LXRa(NR1H3)-dependent amplifier of Abca1 transcription lncRNA gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20200423 MGI PMID:29431742 1618760 Mexis macrophage expressed LXRa(NR1H3)-dependent amplifier of Abca1 transcription lncRNA gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20200423 MGI PMID:29431742 1618760 Mexis macrophage expressed LXRa(NR1H3)-dependent amplifier of Abca1 transcription lncRNA gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20200423 MGI PMID:29431742 1618761 Pdp1 pyruvate dehydrogenase phosphatase catalytic subunit 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1618761 Pdp1 pyruvate dehydrogenase phosphatase catalytic subunit 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1618761 Pdp1 pyruvate dehydrogenase phosphatase catalytic subunit 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1618761 Pdp1 pyruvate dehydrogenase phosphatase catalytic subunit 1 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1618761 Pdp1 pyruvate dehydrogenase phosphatase catalytic subunit 1 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1618761 Pdp1 pyruvate dehydrogenase phosphatase catalytic subunit 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 1618761 Pdp1 pyruvate dehydrogenase phosphatase catalytic subunit 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1618761 Pdp1 pyruvate dehydrogenase phosphatase catalytic subunit 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20201022 MGI 1618761 Pdp1 pyruvate dehydrogenase phosphatase catalytic subunit 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20181227 MGI 1618761 Pdp1 pyruvate dehydrogenase phosphatase catalytic subunit 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1618770 Zfp36l3 zinc finger protein 36, C3H type-like 3 gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20170615 MGI PMID:26952984 1618770 Zfp36l3 zinc finger protein 36, C3H type-like 3 gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20170615 MGI PMID:26952984 1618770 Zfp36l3 zinc finger protein 36, C3H type-like 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20170615 MGI PMID:26952984 1618770 Zfp36l3 zinc finger protein 36, C3H type-like 3 gene MP:0009615 abnormal zinc homeostasis IAGP N RGD:5509061 20170615 MGI PMID:26952984 1618770 Zfp36l3 zinc finger protein 36, C3H type-like 3 gene MP:0010382 abnormal dosage compensation, by inactivation of X chromosome IAGP N RGD:5509061 20170615 MGI PMID:26952984 1618770 Zfp36l3 zinc finger protein 36, C3H type-like 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170615 MGI PMID:26952984 1618770 Zfp36l3 zinc finger protein 36, C3H type-like 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20170615 MGI PMID:26952984 1618773 A4gnt alpha-1,4-N-acetylglucosaminyltransferase gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:22307328 1618773 A4gnt alpha-1,4-N-acetylglucosaminyltransferase gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20200310 MGI PMID:22307328 1618773 A4gnt alpha-1,4-N-acetylglucosaminyltransferase gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20200310 MGI PMID:22307328 1618773 A4gnt alpha-1,4-N-acetylglucosaminyltransferase gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20200310 MGI PMID:22307328 1618773 A4gnt alpha-1,4-N-acetylglucosaminyltransferase gene MP:0005493 stomach epithelial hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:22307328 1618773 A4gnt alpha-1,4-N-acetylglucosaminyltransferase gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20200310 MGI PMID:22307328 1618773 A4gnt alpha-1,4-N-acetylglucosaminyltransferase gene MP:0008010 increased gastric adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:22307328 1618773 A4gnt alpha-1,4-N-acetylglucosaminyltransferase gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20200310 MGI PMID:22307328 1618774 Zdhhc23 zinc finger, DHHC domain containing 23 gene MP:0001314 cornea opacity IEA N RGD:5509061 20181227 MGI 1618774 Zdhhc23 zinc finger, DHHC domain containing 23 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1618774 Zdhhc23 zinc finger, DHHC domain containing 23 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20231207 MGI 1618776 Piwil4 piwi-like RNA-mediated gene silencing 4 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17395546 1618776 Piwil4 piwi-like RNA-mediated gene silencing 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17395546 1618776 Piwil4 piwi-like RNA-mediated gene silencing 4 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17395546 1618776 Piwil4 piwi-like RNA-mediated gene silencing 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22020280 1618776 Piwil4 piwi-like RNA-mediated gene silencing 4 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:17395546 1618776 Piwil4 piwi-like RNA-mediated gene silencing 4 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17395546 1618776 Piwil4 piwi-like RNA-mediated gene silencing 4 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17395546 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0001147 small testis IAGP N RGD:5509061 20210107 MGI PMID:31961863 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20210107 MGI PMID:31961863 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20210107 MGI PMID:31961863 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210107 MGI PMID:31961863 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0003929 decreased heart rate variability IEA N RGD:5509061 20231207 MGI 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20231207 MGI 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20231207 MGI 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210107 MGI PMID:31961863 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20210107 MGI PMID:31961863 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210107 MGI PMID:31961863 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20210107 MGI PMID:31961863 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20210107 MGI PMID:31961863 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20210107 MGI PMID:31961863 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20210107 MGI PMID:31961863 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1618777 Drc7 dynein regulatory complex subunit 7 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20210107 MGI PMID:31961863 1618778 4933402J07Rik RIKEN cDNA 4933402J07 gene gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1618778 4933402J07Rik RIKEN cDNA 4933402J07 gene gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 1618780 Birc7 baculoviral IAP repeat-containing 7 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210826 MGI 1618781 Zfp335 zinc finger protein 335 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:23178126 1618781 Zfp335 zinc finger protein 335 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141127 MGI PMID:25343476 1618781 Zfp335 zinc finger protein 335 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:23178126 1618781 Zfp335 zinc finger protein 335 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141127 MGI PMID:25343476 1618781 Zfp335 zinc finger protein 335 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141127 MGI PMID:25343476 1618781 Zfp335 zinc finger protein 335 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23178126 1618781 Zfp335 zinc finger protein 335 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141127 MGI PMID:25343476 1618781 Zfp335 zinc finger protein 335 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141127 MGI PMID:25343476 1618781 Zfp335 zinc finger protein 335 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141127 MGI PMID:25343476 1618781 Zfp335 zinc finger protein 335 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141127 MGI PMID:25343476 1618781 Zfp335 zinc finger protein 335 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141127 MGI PMID:25343476 1618781 Zfp335 zinc finger protein 335 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141127 MGI PMID:25343476 1618781 Zfp335 zinc finger protein 335 gene MP:0010836 decreased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20141127 MGI PMID:25343476 1618781 Zfp335 zinc finger protein 335 gene MP:0010839 decreased CD8-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20141127 MGI PMID:25343476 1618781 Zfp335 zinc finger protein 335 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23178126 1618781 Zfp335 zinc finger protein 335 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20111116 MGI 1618790 Zfp459 zinc finger protein 459 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1618793 Nutm2 NUT family member 2 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1618795 Gfod1 glucose-fructose oxidoreductase domain containing 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201231 MGI 1618798 A830018L16Rik RIKEN cDNA A830018L16 gene gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1618800 Vwc2l von Willebrand factor C domain-containing protein 2-like gene MP:0001297 microphthalmia IEA N RGD:5509061 20210128 MGI 1618800 Vwc2l von Willebrand factor C domain-containing protein 2-like gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1618803 Trank1 tetratricopeptide repeat and ankyrin repeat containing 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 1618803 Trank1 tetratricopeptide repeat and ankyrin repeat containing 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20240509 MGI PMID:36265442 1618803 Trank1 tetratricopeptide repeat and ankyrin repeat containing 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20240509 MGI PMID:36265442 1618803 Trank1 tetratricopeptide repeat and ankyrin repeat containing 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1618803 Trank1 tetratricopeptide repeat and ankyrin repeat containing 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1618803 Trank1 tetratricopeptide repeat and ankyrin repeat containing 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 1618803 Trank1 tetratricopeptide repeat and ankyrin repeat containing 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20231207 MGI 1618803 Trank1 tetratricopeptide repeat and ankyrin repeat containing 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15064401 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15064401 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0009511 distended stomach IAGP N RGD:5509061 20141003 MGI PMID:14517551 1618804 Itpkb inositol 1,4,5-trisphosphate 3-kinase B gene MP:0013587 absent thymus medulla IAGP N RGD:5509061 20150326 MGI PMID:14517551 1618805 H2bc21 H2B clustered histone 21 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23240083 1618805 H2bc21 H2B clustered histone 21 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20240523 MGI 1618805 H2bc21 H2B clustered histone 21 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23240083 1618805 H2bc21 H2B clustered histone 21 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:23240083 1618805 H2bc21 H2B clustered histone 21 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20240523 MGI 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0000774 decreased brain size IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20220519 MGI 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0001399 hyperactivity IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0002608 increased hematocrit IEA N RGD:5509061 20220811 MGI 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20220519 MGI 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220519 MGI 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220519 MGI 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0020527 small thalamus IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0020870 decreased thigmotaxis IAGP N RGD:5509061 20210211 MGI PMID:31166939 1618834 Lrrc4b leucine rich repeat containing 4B gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:31166939 1618840 Lhfpl4 lipoma HMGIC fusion partner-like protein 4 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1618840 Lhfpl4 lipoma HMGIC fusion partner-like protein 4 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20180524 MGI PMID:28978485 1618840 Lhfpl4 lipoma HMGIC fusion partner-like protein 4 gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:28978485 1618840 Lhfpl4 lipoma HMGIC fusion partner-like protein 4 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:28978485 1618840 Lhfpl4 lipoma HMGIC fusion partner-like protein 4 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:28978485 1618840 Lhfpl4 lipoma HMGIC fusion partner-like protein 4 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20180524 MGI PMID:28978485 1618841 Aak1 AP2 associated kinase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0001469 abnormal contextual conditioning behavior IEA N RGD:5509061 20210128 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20200402 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20181227 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20211021 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20201231 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20201022 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20181227 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20181227 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20200402 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1618841 Aak1 AP2 associated kinase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1618842 Zfp664 zinc finger protein 664 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1618842 Zfp664 zinc finger protein 664 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20201022 MGI 1618843 Mphosph9 M-phase phosphoprotein 9 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20220811 MGI 1618843 Mphosph9 M-phase phosphoprotein 9 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1618843 Mphosph9 M-phase phosphoprotein 9 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20240523 MGI 1618845 Meioc meiosis specific with coiled-coil domain gene MP:0001127 small ovary IAGP N RGD:5509061 20170601 MGI PMID:26742488 1618845 Meioc meiosis specific with coiled-coil domain gene MP:0001147 small testis IAGP N RGD:5509061 20170601 MGI PMID:26742488 1618845 Meioc meiosis specific with coiled-coil domain gene MP:0001925 male infertility IAGP N RGD:5509061 20170601 MGI PMID:26742488 1618845 Meioc meiosis specific with coiled-coil domain gene MP:0001926 female infertility IAGP N RGD:5509061 20170601 MGI PMID:26742488 1618845 Meioc meiosis specific with coiled-coil domain gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20170601 MGI PMID:26742488 1618845 Meioc meiosis specific with coiled-coil domain gene MP:0004805 absent oocytes IAGP N RGD:5509061 20170601 MGI PMID:26742488 1618845 Meioc meiosis specific with coiled-coil domain gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20170601 MGI PMID:26742488 1618845 Meioc meiosis specific with coiled-coil domain gene MP:0005159 azoospermia IAGP N RGD:5509061 20170601 MGI PMID:26742488 1618845 Meioc meiosis specific with coiled-coil domain gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20170601 MGI PMID:26742488 1618845 Meioc meiosis specific with coiled-coil domain gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20170601 MGI PMID:26742488 1618845 Meioc meiosis specific with coiled-coil domain gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20170601 MGI PMID:26742488 1618845 Meioc meiosis specific with coiled-coil domain gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20170601 MGI PMID:26742488 1618845 Meioc meiosis specific with coiled-coil domain gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20170601 MGI PMID:26742488 1618845 Meioc meiosis specific with coiled-coil domain gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20170601 MGI PMID:26742488 1618846 Krt12 keratin 12 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20200310 MGI PMID:26758872 1618846 Krt12 keratin 12 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:16431949 1618846 Krt12 keratin 12 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:26758872 1618846 Krt12 keratin 12 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:8977471 1618846 Krt12 keratin 12 gene MP:0020854 increased cornea epithelium thickness IAGP N RGD:5509061 20200310 MGI PMID:26758872 1618846 Krt12 keratin 12 gene MP:0020855 decreased cornea epithelium thickness IAGP N RGD:5509061 20200310 MGI PMID:8977471 1618846 Krt12 keratin 12 gene MP:0020859 disorganized cornea epithelium IAGP N RGD:5509061 20200310 MGI PMID:26758872 1618847 Rapgefl1 Rap guanine nucleotide exchange factor (GEF)-like 1 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20160804 MGI 1618848 Zfp652 zinc finger protein 652 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1618848 Zfp652 zinc finger protein 652 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1618849 Eme1 essential meiotic structure-specific endonuclease 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20160811 MGI 1618849 Eme1 essential meiotic structure-specific endonuclease 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20201022 MGI 1618849 Eme1 essential meiotic structure-specific endonuclease 1 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20181227 MGI 1618849 Eme1 essential meiotic structure-specific endonuclease 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20230126 MGI PMID:27383418 1618849 Eme1 essential meiotic structure-specific endonuclease 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230126 MGI PMID:27383418 1618849 Eme1 essential meiotic structure-specific endonuclease 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20230126 MGI PMID:27383418 1618849 Eme1 essential meiotic structure-specific endonuclease 1 gene MP:0014040 increased cellular sensitivity to DNA damaging agents IAGP N RGD:5509061 20230126 MGI PMID:27383418 1618851 Leap2 liver-expressed antimicrobial peptide 2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20220929 MGI PMID:34428557 1618851 Leap2 liver-expressed antimicrobial peptide 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20220929 MGI PMID:34428557 1618851 Leap2 liver-expressed antimicrobial peptide 2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20220929 MGI PMID:34428557 1618851 Leap2 liver-expressed antimicrobial peptide 2 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20220929 MGI PMID:34428557 1618851 Leap2 liver-expressed antimicrobial peptide 2 gene MP:0005137 increased growth hormone level IAGP N RGD:5509061 20220929 MGI PMID:34428557 1618851 Leap2 liver-expressed antimicrobial peptide 2 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20220929 MGI PMID:34428557 1618851 Leap2 liver-expressed antimicrobial peptide 2 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20220929 MGI PMID:34428557 1618851 Leap2 liver-expressed antimicrobial peptide 2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20220929 MGI PMID:34428557 1618851 Leap2 liver-expressed antimicrobial peptide 2 gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20220929 MGI PMID:34428557 1618851 Leap2 liver-expressed antimicrobial peptide 2 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20220929 MGI PMID:34428557 1618851 Leap2 liver-expressed antimicrobial peptide 2 gene MP:0031392 hypoactivity IAGP N RGD:5509061 20220929 MGI PMID:34428557 1618933 Odf4 outer dense fiber of sperm tails 4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1618933 Odf4 outer dense fiber of sperm tails 4 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 1618933 Odf4 outer dense fiber of sperm tails 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20230309 MGI PMID:36804949 1618933 Odf4 outer dense fiber of sperm tails 4 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1618933 Odf4 outer dense fiber of sperm tails 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230309 MGI PMID:36804949 1618933 Odf4 outer dense fiber of sperm tails 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230309 MGI PMID:36804949 1618933 Odf4 outer dense fiber of sperm tails 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230309 MGI PMID:36804949 1618933 Odf4 outer dense fiber of sperm tails 4 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20230309 MGI PMID:36804949 1618933 Odf4 outer dense fiber of sperm tails 4 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20230309 MGI PMID:36804949 1618933 Odf4 outer dense fiber of sperm tails 4 gene MP:0013286 abnormal sperm capacitation IAGP N RGD:5509061 20230309 MGI PMID:36804949 1618934 Ackr4 atypical chemokine receptor 4 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20562329 1618934 Ackr4 atypical chemokine receptor 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17485674 1618934 Ackr4 atypical chemokine receptor 4 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:20562329 1618934 Ackr4 atypical chemokine receptor 4 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20562329 1618934 Ackr4 atypical chemokine receptor 4 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20562329 1618934 Ackr4 atypical chemokine receptor 4 gene MP:0008073 abnormal CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20562329 1618934 Ackr4 atypical chemokine receptor 4 gene MP:0008690 increased interleukin-23 secretion IAGP N RGD:5509061 20141003 MGI PMID:20562329 1618934 Ackr4 atypical chemokine receptor 4 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:20562329 1618934 Ackr4 atypical chemokine receptor 4 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:20562329 1618934 Ackr4 atypical chemokine receptor 4 gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:20562329 1618934 Ackr4 atypical chemokine receptor 4 gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20562329 1618935 Dclk3 doublecortin-like kinase 3 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 1618938 Slc23a4 solute carrier family 23 member 4 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20160804 MGI 1618938 Slc23a4 solute carrier family 23 member 4 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15451409 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15706241 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:15240800 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15451409 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15451409 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15240800 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:15240800 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:15706241 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:15240800 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15240800 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:24431439 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0002911 abnormal inhibitory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:15451409 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15240800 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15451409 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15706241 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:15240800 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:15451409 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:15240800 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:15240800 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:24431439 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:15240800 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:24431439 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:24431439 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15240800 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:24431439 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:24431439 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15240800 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0012006 abnormal hippocampus physiology IAGP N RGD:5509061 20141003 MGI PMID:24431439 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0014413 decreased depression-related behavior IAGP N RGD:5509061 20240425 MGI PMID:15706241 1618940 Gabbr2 gamma-aminobutyric acid type B receptor subunit 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:15240800 1618941 Tmem8b transmembrane protein 8B gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210128 MGI 1618941 Tmem8b transmembrane protein 8B gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 1618941 Tmem8b transmembrane protein 8B gene MP:0001258 decreased body length IEA N RGD:5509061 20201022 MGI 1618941 Tmem8b transmembrane protein 8B gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1618941 Tmem8b transmembrane protein 8B gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1618941 Tmem8b transmembrane protein 8B gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1618941 Tmem8b transmembrane protein 8B gene MP:0003883 enlarged stomach IEA N RGD:5509061 20210128 MGI 1618941 Tmem8b transmembrane protein 8B gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1618941 Tmem8b transmembrane protein 8B gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210128 MGI 1618942 Cntnap5b contactin associated protein-like 5B gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230119 MGI 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0001147 small testis IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0001925 male infertility IAGP N RGD:5509061 20200903 MGI PMID:31501240 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0001925 male infertility IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200903 MGI PMID:31501240 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20200903 MGI PMID:31501240 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20200903 MGI PMID:31501240 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20200903 MGI PMID:31501240 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20200903 MGI PMID:31501240 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220303 MGI PMID:31501240 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0031351 abnormal sperm flagellum thickness IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20220317 MGI PMID:31501240 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0031374 abnormal manchette assembly IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20220811 MGI PMID:34231842 1618945 Cfap65 cilia and flagella associated protein 65 gene MP:0031438 abnormal sperm radial spoke morphology IAGP N RGD:5509061 20220915 MGI PMID:34231842 1618946 Catip ciliogenesis associated TTC17 interacting protein gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1618946 Catip ciliogenesis associated TTC17 interacting protein gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1618947 Cd200r4 CD200 receptor 4 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1618950 Mylk4 myosin light chain kinase family, member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240627 MGI PMID:33870126 1618950 Mylk4 myosin light chain kinase family, member 4 gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 1618950 Mylk4 myosin light chain kinase family, member 4 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20240627 MGI PMID:33870126 1618950 Mylk4 myosin light chain kinase family, member 4 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220811 MGI 1618950 Mylk4 myosin light chain kinase family, member 4 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1618950 Mylk4 myosin light chain kinase family, member 4 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1618951 Btn2a2 butyrophilin, subfamily 2, member A2 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20200102 MGI PMID:26809444 1618951 Btn2a2 butyrophilin, subfamily 2, member A2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20200102 MGI PMID:26809444 1618951 Btn2a2 butyrophilin, subfamily 2, member A2 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200102 MGI PMID:26809444 1618951 Btn2a2 butyrophilin, subfamily 2, member A2 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200102 MGI PMID:26809444 1618951 Btn2a2 butyrophilin, subfamily 2, member A2 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20200102 MGI PMID:26809444 1618951 Btn2a2 butyrophilin, subfamily 2, member A2 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20200102 MGI PMID:26809444 1618951 Btn2a2 butyrophilin, subfamily 2, member A2 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20200102 MGI PMID:26809444 1618951 Btn2a2 butyrophilin, subfamily 2, member A2 gene MP:0008896 increased IgG2c level IAGP N RGD:5509061 20200102 MGI PMID:26809444 1618951 Btn2a2 butyrophilin, subfamily 2, member A2 gene MP:0020002 increased response to antigen IAGP N RGD:5509061 20200102 MGI PMID:26809444 1618953 Zc3h12d zinc finger CCCH type containing 12D gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1618953 Zc3h12d zinc finger CCCH type containing 12D gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 1618953 Zc3h12d zinc finger CCCH type containing 12D gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1618953 Zc3h12d zinc finger CCCH type containing 12D gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141106 MGI PMID:24415781 1618953 Zc3h12d zinc finger CCCH type containing 12D gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1618953 Zc3h12d zinc finger CCCH type containing 12D gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141106 MGI PMID:24415781 1618953 Zc3h12d zinc finger CCCH type containing 12D gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141106 MGI PMID:24415781 1618953 Zc3h12d zinc finger CCCH type containing 12D gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141106 MGI PMID:24415781 1618953 Zc3h12d zinc finger CCCH type containing 12D gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20141106 MGI PMID:24415781 1618954 Ccdc170 coiled-coil domain containing 170 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1618957 Fancb Fanconi anemia, complementation group B gene MP:0001147 small testis IAGP N RGD:5509061 20151008 MGI PMID:26123487 1618957 Fancb Fanconi anemia, complementation group B gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20151008 MGI PMID:26123487 1618957 Fancb Fanconi anemia, complementation group B gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20151008 MGI PMID:26123487 1618957 Fancb Fanconi anemia, complementation group B gene MP:0001265 decreased body size IAGP N RGD:5509061 20151008 MGI PMID:26123487 1618957 Fancb Fanconi anemia, complementation group B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20151008 MGI PMID:26123487 1618957 Fancb Fanconi anemia, complementation group B gene MP:0001925 male infertility IAGP N RGD:5509061 20151008 MGI PMID:26123487 1618957 Fancb Fanconi anemia, complementation group B gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20151008 MGI PMID:26123487 1618957 Fancb Fanconi anemia, complementation group B gene MP:0002776 increased Sertoli cell number IAGP N RGD:5509061 20151008 MGI PMID:26123487 1618957 Fancb Fanconi anemia, complementation group B gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20151008 MGI PMID:26123487 1618957 Fancb Fanconi anemia, complementation group B gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20151008 MGI PMID:26123487 1618957 Fancb Fanconi anemia, complementation group B gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20151008 MGI PMID:26123487 1618957 Fancb Fanconi anemia, complementation group B gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20151008 MGI PMID:26123487 1618957 Fancb Fanconi anemia, complementation group B gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20151008 MGI PMID:26123487 1618957 Fancb Fanconi anemia, complementation group B gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:26123487 1618961 Carmil2 capping protein regulator and myosin 1 linker 2 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:23793062 1618961 Carmil2 capping protein regulator and myosin 1 linker 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160421 MGI 1618961 Carmil2 capping protein regulator and myosin 1 linker 2 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23793062 1618961 Carmil2 capping protein regulator and myosin 1 linker 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23793062 1618961 Carmil2 capping protein regulator and myosin 1 linker 2 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20201022 MGI 1618961 Carmil2 capping protein regulator and myosin 1 linker 2 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20210128 MGI 1618961 Carmil2 capping protein regulator and myosin 1 linker 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23793062 1618961 Carmil2 capping protein regulator and myosin 1 linker 2 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:23793062 1618962 Fbxl9 F-box and leucine-rich repeat protein 9 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230601 MGI 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0001200 thick skin IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0001265 decreased body size IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0002764 short tibia IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0004351 short humerus IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0014106 delayed chondrocyte differentiation IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618964 Adamts17 ADAM metallopeptidase with thrombospondin type 1 motif 17 gene MP:0020253 increased collagen level IAGP N RGD:5509061 20201029 MGI PMID:31201465 1618967 Wdtc1 WD and tetratricopeptide repeats 1 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20210128 MGI 1618967 Wdtc1 WD and tetratricopeptide repeats 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1618967 Wdtc1 WD and tetratricopeptide repeats 1 gene MP:0001261 obese IAGP N RGD:5509061 20200310 MGI PMID:17767906 1618967 Wdtc1 WD and tetratricopeptide repeats 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:17767906 1618967 Wdtc1 WD and tetratricopeptide repeats 1 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20201231 MGI 1618967 Wdtc1 WD and tetratricopeptide repeats 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200310 MGI PMID:17767906 1618967 Wdtc1 WD and tetratricopeptide repeats 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:17767906 1618967 Wdtc1 WD and tetratricopeptide repeats 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:17767906 1618967 Wdtc1 WD and tetratricopeptide repeats 1 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20200310 MGI PMID:17767906 1618967 Wdtc1 WD and tetratricopeptide repeats 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17767906 1618967 Wdtc1 WD and tetratricopeptide repeats 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1618968 Themis2 thymocyte selection associated family member 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1618968 Themis2 thymocyte selection associated family member 2 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20160804 MGI 1618968 Themis2 thymocyte selection associated family member 2 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20160804 MGI 1618969 Sesn2 sestrin 2 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:20106877 1618969 Sesn2 sestrin 2 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:22958918 1618969 Sesn2 sestrin 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:22958918 1618969 Sesn2 sestrin 2 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:22958918 1618969 Sesn2 sestrin 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22958918 1618969 Sesn2 sestrin 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22958918 1618969 Sesn2 sestrin 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22958918 1618969 Sesn2 sestrin 2 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:22958918 1618969 Sesn2 sestrin 2 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:20106877 1618969 Sesn2 sestrin 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22958918 1618969 Sesn2 sestrin 2 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:22958918 1618969 Sesn2 sestrin 2 gene MP:0011807 decreased lung fibroblast proliferation IAGP N RGD:5509061 20150212 MGI PMID:20106877 1618969 Sesn2 sestrin 2 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:20106877 1618969 Sesn2 sestrin 2 gene MP:0014174 decreased fatty acid beta-oxidation IAGP N RGD:5509061 20160421 MGI PMID:22958918 1618969 Sesn2 sestrin 2 gene MP:0014388 decreased hepatocyte mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:22958918 1618969 Sesn2 sestrin 2 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:22958918 1618969 Sesn2 sestrin 2 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:22958918 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:21115689 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:21115689 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20240523 MGI 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:21115689 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0001860 liver inflammation IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:21115689 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0002493 increased IgG level IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0002494 increased IgM level IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0002495 increased IgA level IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0003252 abnormal bile duct physiology IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0003254 bile duct inflammation IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20200310 MGI PMID:21115689 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20200310 MGI PMID:21115689 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20200310 MGI PMID:21115689 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20200310 MGI PMID:19322177 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20200310 MGI PMID:21115689 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20200310 MGI PMID:21115689 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20200310 MGI PMID:21115689 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20220811 MGI 1618974 Zc3h12a zinc finger CCCH type containing 12A gene MP:0013611 abnormal bile duct epithelium morphology IAGP N RGD:5509061 20210708 MGI PMID:33513427 1618975 Epha10 Eph receptor A10 gene MP:0001523 impaired righting response IEA N RGD:5509061 20170105 MGI 1618975 Epha10 Eph receptor A10 gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 1618976 Rhbdl2 rhomboid like 2 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1618976 Rhbdl2 rhomboid like 2 gene MP:0001759 increased urine glucose level IEA N RGD:5509061 20240523 MGI 1618976 Rhbdl2 rhomboid like 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1618976 Rhbdl2 rhomboid like 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1618977 Nt5c1a 5'-nucleotidase, cytosolic IA gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20191114 MGI PMID:28325731 1618979 Fhip1a FHF complex subunit HOOK interacting protein 1A gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1618979 Fhip1a FHF complex subunit HOOK interacting protein 1A gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20230601 MGI 1618979 Fhip1a FHF complex subunit HOOK interacting protein 1A gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1618979 Fhip1a FHF complex subunit HOOK interacting protein 1A gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1618979 Fhip1a FHF complex subunit HOOK interacting protein 1A gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 1618979 Fhip1a FHF complex subunit HOOK interacting protein 1A gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1618979 Fhip1a FHF complex subunit HOOK interacting protein 1A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1618981 Ctso cathepsin O gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210128 MGI 1618981 Ctso cathepsin O gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20160421 MGI 1618981 Ctso cathepsin O gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 1618981 Ctso cathepsin O gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20210128 MGI 1618982 Sbspon somatomedin B and thrombospondin, type 1 domain containing gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20200514 MGI 1618982 Sbspon somatomedin B and thrombospondin, type 1 domain containing gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200514 MGI 1618982 Sbspon somatomedin B and thrombospondin, type 1 domain containing gene MP:0001147 small testis IEA N RGD:5509061 20200514 MGI 1618982 Sbspon somatomedin B and thrombospondin, type 1 domain containing gene MP:0001399 hyperactivity IEA N RGD:5509061 20221215 MGI 1618982 Sbspon somatomedin B and thrombospondin, type 1 domain containing gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1618982 Sbspon somatomedin B and thrombospondin, type 1 domain containing gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220519 MGI 1618982 Sbspon somatomedin B and thrombospondin, type 1 domain containing gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220519 MGI 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:23187127 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:23187127 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:18258918 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:23187127 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:18258918 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:18258918 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:18258918 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:18258918 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18258918 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18258918 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18258918 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:23187127 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23187127 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18258918 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:23187127 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:18258918 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:18258918 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:23187127 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18258918 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0008945 hyperchromic macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:18258918 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23187127 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18258918 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18258918 1618983 Flvcr1 feline leukemia virus subgroup C cellular receptor 1 gene MP:0030026 small Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:23187127 1618984 Vash2 vasohibin 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19204325 1618986 Slc27a6 solute carrier family 27 (fatty acid transporter), member 6 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1618987 Cep120 centrosomal protein 120 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0011057 absent brain ependyma motile cilia IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:25251415 1618987 Cep120 centrosomal protein 120 gene MP:0013551 decreased cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20161201 MGI PMID:25251415 1618988 Prdm6 PR domain containing 6 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:24278461 1618988 Prdm6 PR domain containing 6 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:24278461 1618988 Prdm6 PR domain containing 6 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:24278461 1618988 Prdm6 PR domain containing 6 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:24278461 1618988 Prdm6 PR domain containing 6 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:24278461 1618988 Prdm6 PR domain containing 6 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:24278461 1618988 Prdm6 PR domain containing 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24278461 1618988 Prdm6 PR domain containing 6 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24278461 1618988 Prdm6 PR domain containing 6 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24278461 1618988 Prdm6 PR domain containing 6 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24278461 1618993 Tppp2 tubulin polymerization-promoting protein family member 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20191114 MGI PMID:30680919 1618993 Tppp2 tubulin polymerization-promoting protein family member 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20191114 MGI PMID:30680919 1618993 Tppp2 tubulin polymerization-promoting protein family member 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20240523 MGI 1618993 Tppp2 tubulin polymerization-promoting protein family member 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20191114 MGI PMID:30680919 1618993 Tppp2 tubulin polymerization-promoting protein family member 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20191114 MGI PMID:30680919 1618993 Tppp2 tubulin polymerization-promoting protein family member 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20191114 MGI PMID:30680919 1618993 Tppp2 tubulin polymerization-promoting protein family member 2 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20191114 MGI PMID:30680919 1618993 Tppp2 tubulin polymerization-promoting protein family member 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20191114 MGI PMID:30680919 1618995 Eddm3b epididymal protein 3B gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1618995 Eddm3b epididymal protein 3B gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20211021 MGI 1618995 Eddm3b epididymal protein 3B gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1618995 Eddm3b epididymal protein 3B gene MP:0005102 abnormal iris pigmentation IEA N RGD:5509061 20170105 MGI 1618995 Eddm3b epididymal protein 3B gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201022 MGI PMID:32588039 1618996 Pip4p1 phosphatidylinositol-4,5-bisphosphate 4-phosphatase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1618996 Pip4p1 phosphatidylinositol-4,5-bisphosphate 4-phosphatase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:29644770 1618996 Pip4p1 phosphatidylinositol-4,5-bisphosphate 4-phosphatase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:29644770 1618996 Pip4p1 phosphatidylinositol-4,5-bisphosphate 4-phosphatase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29644770 1618996 Pip4p1 phosphatidylinositol-4,5-bisphosphate 4-phosphatase 1 gene MP:0013886 increased CD4-negative, CD25-positive NK T cell number IEA N RGD:5509061 20211021 MGI 1618999 Ahsa1 AHA1, activator of heat shock protein ATPase 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20181227 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20211021 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20200521 MGI PMID:32369453 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20170504 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20200521 MGI PMID:32369453 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20200521 MGI PMID:32369453 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0002725 abnormal vein morphology IEA N RGD:5509061 20170504 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0002947 increased hemangioma incidence IEA N RGD:5509061 20210930 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20200521 MGI PMID:32369453 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20170504 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20200521 MGI PMID:32369453 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0005039 hypoxia IAGP N RGD:5509061 20200521 MGI PMID:32369453 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20200521 MGI PMID:32369453 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20200521 MGI PMID:32369453 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20200521 MGI PMID:32369453 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20170504 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0006080 brain ischemia IAGP N RGD:5509061 20200521 MGI PMID:32369453 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0010022 brain vascular congestion IAGP N RGD:5509061 20200521 MGI PMID:32369453 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200521 MGI PMID:32369453 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200521 MGI PMID:32369453 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20200521 MGI PMID:32369453 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20170504 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0012201 decreased endothelial cell proliferation IAGP N RGD:5509061 20200521 MGI PMID:32369453 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0013843 hepatic portal vein stenosis IEA N RGD:5509061 20170504 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0013852 abnormal Mullerian duct topology IEA N RGD:5509061 20170504 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1619000 Flvcr2 feline leukemia virus subgroup C cellular receptor 2 gene MP:0014018 embryo tumor IEA N RGD:5509061 20170504 MGI 1619001 Nek9 NIMA (never in mitosis gene a)-related expressed kinase 9 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20160114 MGI 1619001 Nek9 NIMA (never in mitosis gene a)-related expressed kinase 9 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1619001 Nek9 NIMA (never in mitosis gene a)-related expressed kinase 9 gene MP:0004259 small placenta IAGP N RGD:5509061 20190912 MGI PMID:29539633 1619001 Nek9 NIMA (never in mitosis gene a)-related expressed kinase 9 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1619001 Nek9 NIMA (never in mitosis gene a)-related expressed kinase 9 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1619001 Nek9 NIMA (never in mitosis gene a)-related expressed kinase 9 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1619001 Nek9 NIMA (never in mitosis gene a)-related expressed kinase 9 gene MP:0009931 abnormal skin appearance IEA N RGD:5509061 20201022 MGI 1619001 Nek9 NIMA (never in mitosis gene a)-related expressed kinase 9 gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20220324 MGI PMID:34078910 1619001 Nek9 NIMA (never in mitosis gene a)-related expressed kinase 9 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1619001 Nek9 NIMA (never in mitosis gene a)-related expressed kinase 9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619001 Nek9 NIMA (never in mitosis gene a)-related expressed kinase 9 gene MP:0011408 renal tubule hypertrophy IAGP N RGD:5509061 20220324 MGI PMID:34078910 1619001 Nek9 NIMA (never in mitosis gene a)-related expressed kinase 9 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20220324 MGI PMID:34078910 1619001 Nek9 NIMA (never in mitosis gene a)-related expressed kinase 9 gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:29539633 1619002 Lin52 lin-52 DREAM MuvB core complex component gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1619002 Lin52 lin-52 DREAM MuvB core complex component gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1619002 Lin52 lin-52 DREAM MuvB core complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619003 Acot6 acyl-CoA thioesterase 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160915 MGI PMID:24652767 1619006 Slc26a10 solute carrier family 26, member 10 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1619006 Slc26a10 solute carrier family 26, member 10 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1619006 Slc26a10 solute carrier family 26, member 10 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20181227 MGI 1619006 Slc26a10 solute carrier family 26, member 10 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21720388 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21720388 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21720388 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21720388 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:21720388 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:20075866 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21720388 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21720388 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:20075866 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21720388 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:20075866 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21720388 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20160317 MGI PMID:20075866 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:20075866 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0010360 decreased liver free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21720388 1619007 Agap2 ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 gene MP:0014126 increased mammary gland apoptosis IAGP N RGD:5509061 20160317 MGI PMID:20075866 1619008 Marchf9 membrane associated ring-CH-type finger 9 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1619008 Marchf9 membrane associated ring-CH-type finger 9 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1619008 Marchf9 membrane associated ring-CH-type finger 9 gene MP:0001391 abnormal tail movements IEA N RGD:5509061 20141003 MGI 1619008 Marchf9 membrane associated ring-CH-type finger 9 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1619008 Marchf9 membrane associated ring-CH-type finger 9 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20141003 MGI 1619008 Marchf9 membrane associated ring-CH-type finger 9 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20160804 MGI 1619009 Kri1 KRI1 homolog gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1619009 Kri1 KRI1 homolog gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619009 Kri1 KRI1 homolog gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1619010 Utp25 UTP25 small subunit processome component gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29262616 1619016 Sprn shadow of prion protein gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20210506 MGI PMID:32317725 1619016 Sprn shadow of prion protein gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:22619325 1619016 Sprn shadow of prion protein gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22619325 1619016 Sprn shadow of prion protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22619325 1619016 Sprn shadow of prion protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22619325 1619016 Sprn shadow of prion protein gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22619325 1619016 Sprn shadow of prion protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210506 MGI PMID:32317725 1619016 Sprn shadow of prion protein gene MP:0001881 abnormal mammary gland physiology IAGP N RGD:5509061 20210506 MGI PMID:32317725 1619016 Sprn shadow of prion protein gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20210506 MGI PMID:32317725 1619016 Sprn shadow of prion protein gene MP:0003314 dysmetria IAGP N RGD:5509061 20141003 MGI PMID:22619325 1619016 Sprn shadow of prion protein gene MP:0003718 maternal effect IAGP N RGD:5509061 20210506 MGI PMID:32317725 1619016 Sprn shadow of prion protein gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20210506 MGI PMID:32317725 1619016 Sprn shadow of prion protein gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20210506 MGI PMID:32317725 1619016 Sprn shadow of prion protein gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20210506 MGI PMID:32317725 1619016 Sprn shadow of prion protein gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20210506 MGI PMID:32317725 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0001925 male infertility IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0001925 male infertility IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20180621 MGI PMID:29449551 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20220811 MGI PMID:28552195 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220317 MGI PMID:29449551 1619017 Cfap44 cilia and flagella associated protein 44 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220811 MGI PMID:28552195 1619019 Mtg1 mitochondrial ribosome-associated GTPase 1 gene MP:0002626 increased heart rate IEA N RGD:5509061 20231207 MGI 1619019 Mtg1 mitochondrial ribosome-associated GTPase 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20191017 MGI PMID:30707992 1619019 Mtg1 mitochondrial ribosome-associated GTPase 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20191017 MGI PMID:30707992 1619019 Mtg1 mitochondrial ribosome-associated GTPase 1 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20191017 MGI PMID:30707992 1619019 Mtg1 mitochondrial ribosome-associated GTPase 1 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20191017 MGI PMID:30707992 1619019 Mtg1 mitochondrial ribosome-associated GTPase 1 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20191017 MGI PMID:30707992 1619019 Mtg1 mitochondrial ribosome-associated GTPase 1 gene MP:0006321 increased myocardial fiber number IAGP N RGD:5509061 20191017 MGI PMID:30707992 1619019 Mtg1 mitochondrial ribosome-associated GTPase 1 gene MP:0010507 shortened RR interval IEA N RGD:5509061 20231207 MGI 1619019 Mtg1 mitochondrial ribosome-associated GTPase 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20191017 MGI PMID:30707992 1619019 Mtg1 mitochondrial ribosome-associated GTPase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619019 Mtg1 mitochondrial ribosome-associated GTPase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1619019 Mtg1 mitochondrial ribosome-associated GTPase 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1619021 Kbtbd7 kelch repeat and BTB (POZ) domain containing 7 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1619021 Kbtbd7 kelch repeat and BTB (POZ) domain containing 7 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1619021 Kbtbd7 kelch repeat and BTB (POZ) domain containing 7 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20181227 MGI 1619021 Kbtbd7 kelch repeat and BTB (POZ) domain containing 7 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20231207 MGI 1619021 Kbtbd7 kelch repeat and BTB (POZ) domain containing 7 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1619021 Kbtbd7 kelch repeat and BTB (POZ) domain containing 7 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1619021 Kbtbd7 kelch repeat and BTB (POZ) domain containing 7 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1619026 Etl4 enhancer trap locus 4 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:16204209 1619026 Etl4 enhancer trap locus 4 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619026 Etl4 enhancer trap locus 4 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619026 Etl4 enhancer trap locus 4 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:16204209 1619026 Etl4 enhancer trap locus 4 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619026 Etl4 enhancer trap locus 4 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:16204209 1619026 Etl4 enhancer trap locus 4 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619026 Etl4 enhancer trap locus 4 gene MP:0001257 increased body length IEA N RGD:5509061 20230601 MGI 1619026 Etl4 enhancer trap locus 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619026 Etl4 enhancer trap locus 4 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16204209 1619026 Etl4 enhancer trap locus 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16204209 1619026 Etl4 enhancer trap locus 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619026 Etl4 enhancer trap locus 4 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16204209 1619026 Etl4 enhancer trap locus 4 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619026 Etl4 enhancer trap locus 4 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:16204209 1619026 Etl4 enhancer trap locus 4 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619026 Etl4 enhancer trap locus 4 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619026 Etl4 enhancer trap locus 4 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619026 Etl4 enhancer trap locus 4 gene MP:0003129 persistent cloaca IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619026 Etl4 enhancer trap locus 4 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619026 Etl4 enhancer trap locus 4 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:16204209 1619026 Etl4 enhancer trap locus 4 gene MP:0004659 abnormal odontoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619026 Etl4 enhancer trap locus 4 gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:16204209 1619026 Etl4 enhancer trap locus 4 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619026 Etl4 enhancer trap locus 4 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:16204209 1619026 Etl4 enhancer trap locus 4 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619026 Etl4 enhancer trap locus 4 gene MP:0004710 small notochord IAGP N RGD:5509061 20141003 MGI PMID:16204209 1619026 Etl4 enhancer trap locus 4 gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20141003 MGI PMID:16204209 1619026 Etl4 enhancer trap locus 4 gene MP:0006392 abnormal nucleus pulposus morphology IAGP N RGD:5509061 20141003 MGI PMID:16204209 1619026 Etl4 enhancer trap locus 4 gene MP:0006392 abnormal nucleus pulposus morphology IAGP N RGD:5509061 20141003 MGI PMID:22522943 1619026 Etl4 enhancer trap locus 4 gene MP:0006393 absent nucleus pulposus IAGP N RGD:5509061 20141003 MGI PMID:16204209 1619026 Etl4 enhancer trap locus 4 gene MP:0010770 preweaning lethality IAGP N RGD:5509061 20141003 MGI PMID:22522943 1619026 Etl4 enhancer trap locus 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9706697 1619027 Tmem212 transmembrane protein 212 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20230601 MGI 1619027 Tmem212 transmembrane protein 212 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20230601 MGI 1619027 Tmem212 transmembrane protein 212 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20230601 MGI 1619027 Tmem212 transmembrane protein 212 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20200416 MGI PMID:31485013 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200416 MGI PMID:31485013 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200416 MGI PMID:31485013 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20200416 MGI PMID:31485013 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20200416 MGI PMID:31485013 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20200416 MGI PMID:31485013 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20230601 MGI 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20200416 MGI PMID:31485013 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20200416 MGI PMID:31485013 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20200416 MGI PMID:31485013 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20200416 MGI PMID:31485013 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201231 MGI 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20231207 MGI 1619028 Elfn2 leucine rich repeat and fibronectin type III, extracellular 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1619029 Fam120c family with sequence similarity 120, member C gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1619029 Fam120c family with sequence similarity 120, member C gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1619029 Fam120c family with sequence similarity 120, member C gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20230601 MGI 1619029 Fam120c family with sequence similarity 120, member C gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20230601 MGI 1619029 Fam120c family with sequence similarity 120, member C gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1619029 Fam120c family with sequence similarity 120, member C gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1619029 Fam120c family with sequence similarity 120, member C gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1619029 Fam120c family with sequence similarity 120, member C gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1619029 Fam120c family with sequence similarity 120, member C gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1619029 Fam120c family with sequence similarity 120, member C gene MP:0003917 increased kidney weight IEA N RGD:5509061 20230601 MGI 1619030 Hs3st2 heparan sulfate (glucosamine) 3-O-sulfotransferase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18839409 1619031 Tet3 tet methylcytosine dioxygenase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20230316 MGI PMID:35304452 1619031 Tet3 tet methylcytosine dioxygenase 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20230316 MGI PMID:35304452 1619031 Tet3 tet methylcytosine dioxygenase 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:21892189 1619031 Tet3 tet methylcytosine dioxygenase 3 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:21892189 1619031 Tet3 tet methylcytosine dioxygenase 3 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20230316 MGI PMID:35304452 1619031 Tet3 tet methylcytosine dioxygenase 3 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21892189 1619031 Tet3 tet methylcytosine dioxygenase 3 gene MP:0013771 decreased effector memory T-helper cell number IAGP N RGD:5509061 20230316 MGI PMID:35304452 1619032 Vps37d vacuolar protein sorting 37D gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1619032 Vps37d vacuolar protein sorting 37D gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1619032 Vps37d vacuolar protein sorting 37D gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20160811 MGI 1619032 Vps37d vacuolar protein sorting 37D gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1619032 Vps37d vacuolar protein sorting 37D gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1619032 Vps37d vacuolar protein sorting 37D gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619032 Vps37d vacuolar protein sorting 37D gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20170105 MGI 1619036 Pirt phosphoinositide-interacting regulator of transient receptor potential channels gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:18455988 1619036 Pirt phosphoinositide-interacting regulator of transient receptor potential channels gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20151217 MGI PMID:24462040 1619036 Pirt phosphoinositide-interacting regulator of transient receptor potential channels gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:18455988 1619036 Pirt phosphoinositide-interacting regulator of transient receptor potential channels gene MP:0009253 abnormal sympathetic neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18455988 1619042 1700102P08Rik RIKEN cDNA 1700102P08 gene gene MP:0001147 small testis IAGP N RGD:5509061 20210415 MGI PMID:31930642 1619042 1700102P08Rik RIKEN cDNA 1700102P08 gene gene MP:0001925 male infertility IAGP N RGD:5509061 20210415 MGI PMID:31930642 1619042 1700102P08Rik RIKEN cDNA 1700102P08 gene gene MP:0004930 small epididymis IAGP N RGD:5509061 20210415 MGI PMID:31930642 1619042 1700102P08Rik RIKEN cDNA 1700102P08 gene gene MP:0005159 azoospermia IAGP N RGD:5509061 20210415 MGI PMID:31930642 1619042 1700102P08Rik RIKEN cDNA 1700102P08 gene gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20210415 MGI PMID:31930642 1619042 1700102P08Rik RIKEN cDNA 1700102P08 gene gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20210415 MGI PMID:31930642 1619048 C7 complement component 7 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1619048 C7 complement component 7 gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20240523 MGI 1619048 C7 complement component 7 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1619048 C7 complement component 7 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1619048 C7 complement component 7 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20240523 MGI 1619048 C7 complement component 7 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1619050 Arhgef18 Rho/Rac guanine nucleotide exchange factor 18 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1619050 Arhgef18 Rho/Rac guanine nucleotide exchange factor 18 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1619050 Arhgef18 Rho/Rac guanine nucleotide exchange factor 18 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619050 Arhgef18 Rho/Rac guanine nucleotide exchange factor 18 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20141003 MGI 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20368432 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20074529 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20368432 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20074529 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20368432 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:20368432 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20190815 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:20368432 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:20368432 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:20368432 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20190815 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20190815 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:20368432 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20190815 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:20074529 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:20074529 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:11283375 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:20074529 1619056 Acacb acetyl-Coenzyme A carboxylase beta gene MP:0014173 increased fatty acid beta-oxidation IAGP N RGD:5509061 20160421 MGI PMID:11283375 1619058 Golga2 golgin A2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20191017 MGI PMID:29128360 1619058 Golga2 golgin A2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20191017 MGI PMID:29128360 1619058 Golga2 golgin A2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0001147 small testis IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20191017 MGI PMID:29128360 1619058 Golga2 golgin A2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20191017 MGI PMID:29128360 1619058 Golga2 golgin A2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191017 MGI PMID:29128360 1619058 Golga2 golgin A2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0001393 ataxia IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0001925 male infertility IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0002083 premature death IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0002083 premature death IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20191017 MGI PMID:29128360 1619058 Golga2 golgin A2 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20191017 MGI PMID:29128360 1619058 Golga2 golgin A2 gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20191017 MGI PMID:29128360 1619058 Golga2 golgin A2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20191017 MGI PMID:29128360 1619058 Golga2 golgin A2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20191017 MGI PMID:29128360 1619058 Golga2 golgin A2 gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0014228 increased alveolar macrophage number IAGP N RGD:5509061 20191017 MGI PMID:29128360 1619058 Golga2 golgin A2 gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0020850 abnormal microtubule cytoskeleton morphology IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0030949 abnormal Golgi vesicle transport IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0030953 abnormal Golgi cisterna morphology IAGP N RGD:5509061 20190919 MGI PMID:28028212 1619058 Golga2 golgin A2 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619058 Golga2 golgin A2 gene MP:0031355 abnormal proacrosomal vesicle fusion IAGP N RGD:5509061 20220317 MGI PMID:28055014 1619059 Dcaf8 DDB1 and CUL4 associated factor 8 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200514 MGI 1619059 Dcaf8 DDB1 and CUL4 associated factor 8 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200514 MGI 1619059 Dcaf8 DDB1 and CUL4 associated factor 8 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20200514 MGI 1619059 Dcaf8 DDB1 and CUL4 associated factor 8 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200514 MGI 1619059 Dcaf8 DDB1 and CUL4 associated factor 8 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200514 MGI 1619059 Dcaf8 DDB1 and CUL4 associated factor 8 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1619059 Dcaf8 DDB1 and CUL4 associated factor 8 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210729 MGI PMID:33730447 1619059 Dcaf8 DDB1 and CUL4 associated factor 8 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1619059 Dcaf8 DDB1 and CUL4 associated factor 8 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 1619059 Dcaf8 DDB1 and CUL4 associated factor 8 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210729 MGI PMID:33730447 1619059 Dcaf8 DDB1 and CUL4 associated factor 8 gene MP:0010895 increased lung compliance IEA N RGD:5509061 20210128 MGI 1619059 Dcaf8 DDB1 and CUL4 associated factor 8 gene MP:0011045 decreased lung elastance IEA N RGD:5509061 20210128 MGI 1619059 Dcaf8 DDB1 and CUL4 associated factor 8 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1619059 Dcaf8 DDB1 and CUL4 associated factor 8 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210729 MGI PMID:33730447 1619059 Dcaf8 DDB1 and CUL4 associated factor 8 gene MP:0031436 decreased copulatory plug deposition IAGP N RGD:5509061 20220922 MGI PMID:33730447 1619060 Tmem132a transmembrane protein 132A gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20160811 MGI 1619060 Tmem132a transmembrane protein 132A gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20170105 MGI 1619060 Tmem132a transmembrane protein 132A gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0000564 syndactyly IEA N RGD:5509061 20210520 MGI 1619060 Tmem132a transmembrane protein 132A gene MP:0000929 open neural tube IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1619060 Tmem132a transmembrane protein 132A gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1619060 Tmem132a transmembrane protein 132A gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20160811 MGI 1619060 Tmem132a transmembrane protein 132A gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20160811 MGI 1619060 Tmem132a transmembrane protein 132A gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0003054 spina bifida IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0003675 kidney cyst IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20160811 MGI 1619060 Tmem132a transmembrane protein 132A gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20160811 MGI 1619060 Tmem132a transmembrane protein 132A gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1619060 Tmem132a transmembrane protein 132A gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0005034 abnormal anus morphology IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20160811 MGI 1619060 Tmem132a transmembrane protein 132A gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1619060 Tmem132a transmembrane protein 132A gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20190502 MGI 1619060 Tmem132a transmembrane protein 132A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619060 Tmem132a transmembrane protein 132A gene MP:0011495 abnormal head shape IEA N RGD:5509061 20160811 MGI 1619060 Tmem132a transmembrane protein 132A gene MP:0012707 incomplete caudal neuropore closure IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0013166 small forelimb buds IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0013169 small hindlimb buds IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0013956 decreased colon length IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619060 Tmem132a transmembrane protein 132A gene MP:0014282 forelimb syndactyly IAGP N RGD:5509061 20241031 MGI PMID:39385148 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0000167 decreased chondrocyte number IEA N RGD:5509061 20200310 MGI 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0001262 decreased body weight IEA N RGD:5509061 20210520 MGI 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20210520 MGI 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210520 MGI 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:15719068 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20200310 MGI PMID:15719068 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0002936 joint swelling IAGP N RGD:5509061 20200310 MGI PMID:15719068 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20200310 MGI PMID:15719068 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0003200 calcified joint IAGP N RGD:5509061 20200310 MGI PMID:15719068 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0003807 camptodactyly IAGP N RGD:5509061 20200310 MGI PMID:15719068 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20230720 MGI 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0005508 abnormal skeleton morphology IEA N RGD:5509061 20200310 MGI 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210520 MGI 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:15719068 1619061 Prg4 proteoglycan 4 (megakaryocyte stimulating factor, articular superficial zone protein) gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210520 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:1936982 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1936982 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20151022 MGI PMID:25677649 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240627 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160421 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:1936982 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20151022 MGI PMID:23261874 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20151022 MGI PMID:18984010 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:1936982 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:12923531 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IEA N RGD:5509061 20111116 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0005098 abnormal optic choroid morphology IAGP N RGD:5509061 20141003 MGI PMID:12923531 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0005102 abnormal iris pigmentation IEA N RGD:5509061 20160421 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0005172 decreased eye pigmentation IEA N RGD:5509061 20111116 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12923531 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:12923531 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20220721 MGI PMID:33513603 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20240523 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20201001 MGI PMID:1936982 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20151022 MGI PMID:25677649 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0009455 enhanced cued conditioning behavior IAGP N RGD:5509061 20151022 MGI PMID:18984010 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:12923531 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0010193 abnormal choroid melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:12923531 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20151022 MGI PMID:18984010 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0013894 abnormal behavioral response to amphetamine IAGP N RGD:5509061 20151022 MGI PMID:18984010 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:18984010 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170720 MGI PMID:1936982 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20220721 MGI PMID:12923531 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:25677649 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0020916 increased susceptibility to Herpesvirales infection IEA N RGD:5509061 20200430 MGI 1619063 Dtnbp1 dystrobrevin binding protein 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:25677649 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:19679836 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19679836 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:23719809 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20230126 MGI PMID:36197846 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19679836 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:23719809 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:23055483 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19679836 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:19679836 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:24101523 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:23719809 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19679836 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19679836 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:24101523 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18469815 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:18469815 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:23719809 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20230126 MGI PMID:36197846 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:18469815 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:19679836 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17259983 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23719809 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20141003 MGI PMID:23719809 1619064 Dgcr8 DGCR8, microprocessor complex subunit gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20141003 MGI PMID:24101523 1619065 Col4a6 collagen, type IV, alpha 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17418794 1619071 Brd8 bromodomain containing 8 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1619071 Brd8 bromodomain containing 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619075 Spaca7 sperm acrosome associated 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1619079 Acap2 ArfGAP with coiled-coil, ankyrin repeat and PH domains 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1619081 Uvrag UV radiation resistance associated gene gene MP:0000274 enlarged heart IAGP N RGD:5509061 20200310 MGI PMID:24081163 1619081 Uvrag UV radiation resistance associated gene gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20200310 MGI PMID:24081163 1619081 Uvrag UV radiation resistance associated gene gene MP:0001853 heart inflammation IAGP N RGD:5509061 20200310 MGI PMID:24081163 1619081 Uvrag UV radiation resistance associated gene gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20200310 MGI PMID:24081163 1619081 Uvrag UV radiation resistance associated gene gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20200310 MGI PMID:24081163 1619081 Uvrag UV radiation resistance associated gene gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20200310 MGI PMID:24081163 1619081 Uvrag UV radiation resistance associated gene gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:24081163 1619081 Uvrag UV radiation resistance associated gene gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:24081163 1619081 Uvrag UV radiation resistance associated gene gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20200310 MGI PMID:24081163 1619081 Uvrag UV radiation resistance associated gene gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20200310 MGI PMID:24081163 1619081 Uvrag UV radiation resistance associated gene gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20200310 MGI PMID:24081163 1619081 Uvrag UV radiation resistance associated gene gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20200310 MGI PMID:24081163 1619081 Uvrag UV radiation resistance associated gene gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20200310 MGI PMID:24081163 1619082 Axdnd1 axonemal dynein light chain domain containing 1 gene MP:0001147 small testis IAGP N RGD:5509061 20220721 MGI PMID:35386379 1619082 Axdnd1 axonemal dynein light chain domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220721 MGI PMID:35386379 1619082 Axdnd1 axonemal dynein light chain domain containing 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220721 MGI PMID:35386379 1619082 Axdnd1 axonemal dynein light chain domain containing 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220721 MGI PMID:35386379 1619082 Axdnd1 axonemal dynein light chain domain containing 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220721 MGI PMID:35386379 1619082 Axdnd1 axonemal dynein light chain domain containing 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220721 MGI PMID:35386379 1619082 Axdnd1 axonemal dynein light chain domain containing 1 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20220721 MGI PMID:35386379 1619082 Axdnd1 axonemal dynein light chain domain containing 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220721 MGI PMID:35386379 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:24247431 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20170223 MGI PMID:27045955 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20170223 MGI PMID:27045955 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20170223 MGI PMID:27045955 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24247431 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20170223 MGI PMID:27045955 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:24247431 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20170223 MGI PMID:27045955 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20170223 MGI PMID:27045955 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0003288 intestinal edema IAGP N RGD:5509061 20170223 MGI PMID:27045955 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20170223 MGI PMID:27045955 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20170223 MGI PMID:27045955 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:24247431 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24247431 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24247431 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0011707 impaired fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:24247431 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20141003 MGI PMID:24247431 1619084 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20170223 MGI PMID:27045955 1619087 Jakmip1 janus kinase and microtubule interacting protein 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20160310 MGI PMID:26627310 1619087 Jakmip1 janus kinase and microtubule interacting protein 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20160310 MGI PMID:26627310 1619087 Jakmip1 janus kinase and microtubule interacting protein 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160310 MGI PMID:26627310 1619087 Jakmip1 janus kinase and microtubule interacting protein 1 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20160310 MGI PMID:26627310 1619087 Jakmip1 janus kinase and microtubule interacting protein 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20160310 MGI PMID:26627310 1619087 Jakmip1 janus kinase and microtubule interacting protein 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20160310 MGI PMID:26627310 1619087 Jakmip1 janus kinase and microtubule interacting protein 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20160310 MGI PMID:26627310 1619087 Jakmip1 janus kinase and microtubule interacting protein 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20160310 MGI PMID:26627310 1619087 Jakmip1 janus kinase and microtubule interacting protein 1 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20160310 MGI PMID:26627310 1619087 Jakmip1 janus kinase and microtubule interacting protein 1 gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20160310 MGI PMID:26627310 1619087 Jakmip1 janus kinase and microtubule interacting protein 1 gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20160310 MGI PMID:26627310 1619087 Jakmip1 janus kinase and microtubule interacting protein 1 gene MP:0013140 excessive vocalization IAGP N RGD:5509061 20160310 MGI PMID:26627310 1619087 Jakmip1 janus kinase and microtubule interacting protein 1 gene MP:0021117 abnormal huddling behavior IAGP N RGD:5509061 20220519 MGI PMID:26627310 1619089 Ccdc125 coiled-coil domain containing 125 gene MP:0000745 tremors IEA N RGD:5509061 20210520 MGI 1619089 Ccdc125 coiled-coil domain containing 125 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20240523 MGI 1619094 Hhatl hedgehog acyltransferase-like gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1619094 Hhatl hedgehog acyltransferase-like gene MP:0001258 decreased body length IEA N RGD:5509061 20240523 MGI 1619094 Hhatl hedgehog acyltransferase-like gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210826 MGI 1619094 Hhatl hedgehog acyltransferase-like gene MP:0001406 abnormal gait IEA N RGD:5509061 20200310 MGI 1619094 Hhatl hedgehog acyltransferase-like gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1619094 Hhatl hedgehog acyltransferase-like gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20210128 MGI 1619094 Hhatl hedgehog acyltransferase-like gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20231207 MGI 1619094 Hhatl hedgehog acyltransferase-like gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1619094 Hhatl hedgehog acyltransferase-like gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1619094 Hhatl hedgehog acyltransferase-like gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1619094 Hhatl hedgehog acyltransferase-like gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1619095 Mdga1 MAM domain containing glycosylphosphatidylinositol anchor 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20200310 MGI PMID:21104742 1619097 Dnaaf6rt dynein axonemal assembly factor 6, retrotransposed gene MP:0001925 male infertility IAGP N RGD:5509061 20150122 MGI PMID:24421334 1619097 Dnaaf6rt dynein axonemal assembly factor 6, retrotransposed gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20150122 MGI PMID:24421334 1619097 Dnaaf6rt dynein axonemal assembly factor 6, retrotransposed gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150122 MGI PMID:24421334 1619097 Dnaaf6rt dynein axonemal assembly factor 6, retrotransposed gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20150122 MGI PMID:24421334 1619097 Dnaaf6rt dynein axonemal assembly factor 6, retrotransposed gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20150122 MGI PMID:24421334 1619097 Dnaaf6rt dynein axonemal assembly factor 6, retrotransposed gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20150122 MGI PMID:24421334 1619097 Dnaaf6rt dynein axonemal assembly factor 6, retrotransposed gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20150122 MGI PMID:24421334 1619097 Dnaaf6rt dynein axonemal assembly factor 6, retrotransposed gene MP:0009242 thin sperm flagellum IAGP N RGD:5509061 20150122 MGI PMID:24421334 1619097 Dnaaf6rt dynein axonemal assembly factor 6, retrotransposed gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20150122 MGI PMID:24421334 1619099 Ccdc7a coiled-coil domain containing 7A gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20668205 1619099 Ccdc7a coiled-coil domain containing 7A gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:24011076 1619099 Ccdc7a coiled-coil domain containing 7A gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:24011076 1619099 Ccdc7a coiled-coil domain containing 7A gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:20668205 1619099 Ccdc7a coiled-coil domain containing 7A gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:24011076 1619099 Ccdc7a coiled-coil domain containing 7A gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:24011076 1619099 Ccdc7a coiled-coil domain containing 7A gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:24011076 1619099 Ccdc7a coiled-coil domain containing 7A gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:20668205 1619099 Ccdc7a coiled-coil domain containing 7A gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:24011076 1619099 Ccdc7a coiled-coil domain containing 7A gene MP:0011614 slow aging IAGP N RGD:5509061 20141003 MGI PMID:24011076 1619099 Ccdc7a coiled-coil domain containing 7A gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:24011076 1619099 Ccdc7a coiled-coil domain containing 7A gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:24011076 1619099 Ccdc7a coiled-coil domain containing 7A gene MP:0012289 abnormal non-rapid eye movement sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:24011076 1619099 Ccdc7a coiled-coil domain containing 7A gene MP:0012297 hyperactivity elicited by feed restriction IAGP N RGD:5509061 20141003 MGI PMID:20668205 1619101 Mipol1 mirror-image polydactyly 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1619101 Mipol1 mirror-image polydactyly 1 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1619101 Mipol1 mirror-image polydactyly 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20181227 MGI 1619101 Mipol1 mirror-image polydactyly 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1619101 Mipol1 mirror-image polydactyly 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1619101 Mipol1 mirror-image polydactyly 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1619101 Mipol1 mirror-image polydactyly 1 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 1619102 Spata18 spermatogenesis associated 18 gene MP:0001577 anemia IAGP N RGD:5509061 20180329 MGI PMID:26216032 1619102 Spata18 spermatogenesis associated 18 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20180329 MGI PMID:26216032 1619102 Spata18 spermatogenesis associated 18 gene MP:0002083 premature death IAGP N RGD:5509061 20180329 MGI PMID:26216032 1619102 Spata18 spermatogenesis associated 18 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20180329 MGI PMID:26216032 1619102 Spata18 spermatogenesis associated 18 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20180329 MGI PMID:26216032 1619102 Spata18 spermatogenesis associated 18 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20180329 MGI PMID:26216032 1619102 Spata18 spermatogenesis associated 18 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20180329 MGI PMID:26216032 1619102 Spata18 spermatogenesis associated 18 gene MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20180329 MGI PMID:26216032 1619102 Spata18 spermatogenesis associated 18 gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20180329 MGI PMID:26216032 1619102 Spata18 spermatogenesis associated 18 gene MP:0010273 increased classified tumor incidence IAGP N RGD:5509061 20180329 MGI PMID:26216032 1619102 Spata18 spermatogenesis associated 18 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20180329 MGI PMID:26216032 1619103 Ms4a13 membrane-spanning 4-domains, subfamily A, member 13 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1619104 C2cd6 C2 calcium dependent domain containing 6 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220113 MGI PMID:34919125 1619104 C2cd6 C2 calcium dependent domain containing 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20220113 MGI PMID:34919125 1619104 C2cd6 C2 calcium dependent domain containing 6 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220113 MGI PMID:34919125 1619104 C2cd6 C2 calcium dependent domain containing 6 gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20220113 MGI PMID:34919125 1619105 Izumo1 izumo sperm-egg fusion 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:15759005 1619105 Izumo1 izumo sperm-egg fusion 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15759005 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0003230 abnormal umbilical artery morphology IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0003584 bifid ureter IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0004111 abnormal coronary artery morphology IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0006093 arteriovenous malformation IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0008922 abnormal cervical rib IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0012303 umbilical vein stenosis IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0013842 ductus venosus stenosis IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0013843 hepatic portal vein stenosis IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0013985 abnormal umbilical vein topology IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0013987 absent intrahepatic inferior vena cava segment IEA N RGD:5509061 20170504 MGI 1619106 1700067K01Rik RIKEN cDNA 1700067K01 gene gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1619112 Ccsap centriole, cilia and spindle associated protein gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1619112 Ccsap centriole, cilia and spindle associated protein gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1619112 Ccsap centriole, cilia and spindle associated protein gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220811 MGI 1619116 Fbxl20 F-box and leucine-rich repeat protein 20 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17803915 1619116 Fbxl20 F-box and leucine-rich repeat protein 20 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17803915 1619116 Fbxl20 F-box and leucine-rich repeat protein 20 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20181227 MGI 1619116 Fbxl20 F-box and leucine-rich repeat protein 20 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 1619116 Fbxl20 F-box and leucine-rich repeat protein 20 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:17803915 1619116 Fbxl20 F-box and leucine-rich repeat protein 20 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:17803915 1619116 Fbxl20 F-box and leucine-rich repeat protein 20 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17803915 1619116 Fbxl20 F-box and leucine-rich repeat protein 20 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17803915 1619116 Fbxl20 F-box and leucine-rich repeat protein 20 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1619117 Scaf11 SR-related CTD-associated factor 11 gene MP:0003036 vertebral transformation IEA N RGD:5509061 20200310 MGI 1619117 Scaf11 SR-related CTD-associated factor 11 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20200310 MGI 1619117 Scaf11 SR-related CTD-associated factor 11 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1619118 2510009E07Rik RIKEN cDNA 2510009E07 gene gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200514 MGI 1619118 2510009E07Rik RIKEN cDNA 2510009E07 gene gene MP:0000274 enlarged heart IEA N RGD:5509061 20200514 MGI 1619118 2510009E07Rik RIKEN cDNA 2510009E07 gene gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20200514 MGI 1619118 2510009E07Rik RIKEN cDNA 2510009E07 gene gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20200514 MGI 1619118 2510009E07Rik RIKEN cDNA 2510009E07 gene gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20200514 MGI 1619118 2510009E07Rik RIKEN cDNA 2510009E07 gene gene MP:0000642 enlarged adrenal glands IEA N RGD:5509061 20200514 MGI 1619118 2510009E07Rik RIKEN cDNA 2510009E07 gene gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1619118 2510009E07Rik RIKEN cDNA 2510009E07 gene gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1619118 2510009E07Rik RIKEN cDNA 2510009E07 gene gene MP:0003068 enlarged kidney IEA N RGD:5509061 20200514 MGI 1619120 Zfp157 zinc finger protein 157 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:22588720 1619120 Zfp157 zinc finger protein 157 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:22588720 1619120 Zfp157 zinc finger protein 157 gene MP:0001881 abnormal mammary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:22588720 1619120 Zfp157 zinc finger protein 157 gene MP:0001884 mammary gland alveolar hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22588720 1619120 Zfp157 zinc finger protein 157 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:22588720 1619120 Zfp157 zinc finger protein 157 gene MP:0013781 abnormal mammary gland luminal epithelium morphology IAGP N RGD:5509061 20150625 MGI PMID:22588720 1619121 Tdrp testis development related protein gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1619121 Tdrp testis development related protein gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1619121 Tdrp testis development related protein gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20160811 MGI 1619121 Tdrp testis development related protein gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20210826 MGI PMID:27069551 1619121 Tdrp testis development related protein gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20160811 MGI 1619121 Tdrp testis development related protein gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210128 MGI 1619121 Tdrp testis development related protein gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210826 MGI PMID:27069551 1619121 Tdrp testis development related protein gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210826 MGI PMID:27069551 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0001258 decreased body length IEA N RGD:5509061 20170323 MGI 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20170323 MGI 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0003889 enhanced sensorimotor gating IEA N RGD:5509061 20170323 MGI 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 1619123 Chst14 carbohydrate sulfotransferase 14 gene MP:0011906 increased Schwann cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23360803 1619124 Pygo1 pygopus 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17425782 1619124 Pygo1 pygopus 1 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:17428831 1619124 Pygo1 pygopus 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17425782 1619124 Pygo1 pygopus 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23637336 1619124 Pygo1 pygopus 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23637336 1619124 Pygo1 pygopus 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17425782 1619124 Pygo1 pygopus 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17428831 1619124 Pygo1 pygopus 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23637336 1619124 Pygo1 pygopus 1 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:17425782 1619124 Pygo1 pygopus 1 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:17425782 1619124 Pygo1 pygopus 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:17425782 1619124 Pygo1 pygopus 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17425782 1619124 Pygo1 pygopus 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:23637336 1619124 Pygo1 pygopus 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17425782 1619124 Pygo1 pygopus 1 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:17425782 1619125 2610008E11Rik RIKEN cDNA 2610008E11 gene gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1619125 2610008E11Rik RIKEN cDNA 2610008E11 gene gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1619125 2610008E11Rik RIKEN cDNA 2610008E11 gene gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1619125 2610008E11Rik RIKEN cDNA 2610008E11 gene gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1619125 2610008E11Rik RIKEN cDNA 2610008E11 gene gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1619125 2610008E11Rik RIKEN cDNA 2610008E11 gene gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1619125 2610008E11Rik RIKEN cDNA 2610008E11 gene gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1619125 2610008E11Rik RIKEN cDNA 2610008E11 gene gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1619125 2610008E11Rik RIKEN cDNA 2610008E11 gene gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1619127 Seh1l SEH1-like (S. cerevisiae gene MP:0000745 tremors IAGP N RGD:5509061 20210617 MGI PMID:30876848 1619127 Seh1l SEH1-like (S. cerevisiae gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20210617 MGI PMID:30876848 1619127 Seh1l SEH1-like (S. cerevisiae gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20210617 MGI PMID:30876848 1619127 Seh1l SEH1-like (S. cerevisiae gene MP:0001393 ataxia IAGP N RGD:5509061 20210617 MGI PMID:30876848 1619127 Seh1l SEH1-like (S. cerevisiae gene MP:0002064 seizures IAGP N RGD:5509061 20210617 MGI PMID:30876848 1619127 Seh1l SEH1-like (S. cerevisiae gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20210617 MGI PMID:30876848 1619127 Seh1l SEH1-like (S. cerevisiae gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20210617 MGI PMID:30876848 1619127 Seh1l SEH1-like (S. cerevisiae gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210617 MGI PMID:30876848 1619127 Seh1l SEH1-like (S. cerevisiae gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210617 MGI PMID:30876848 1619127 Seh1l SEH1-like (S. cerevisiae gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619127 Seh1l SEH1-like (S. cerevisiae gene MP:0013438 dysmyelination IAGP N RGD:5509061 20210617 MGI PMID:30876848 1619128 Dennd2d DENN domain containing 2D gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1619128 Dennd2d DENN domain containing 2D gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1619129 Ddhd2 DDHD domain containing 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:25267624 1619129 Ddhd2 DDHD domain containing 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20200310 MGI PMID:25267624 1619129 Ddhd2 DDHD domain containing 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20200310 MGI PMID:25267624 1619129 Ddhd2 DDHD domain containing 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20200310 MGI PMID:25267624 1619129 Ddhd2 DDHD domain containing 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20200310 MGI PMID:25267624 1619129 Ddhd2 DDHD domain containing 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:25267624 1619129 Ddhd2 DDHD domain containing 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20200310 MGI PMID:25267624 1619129 Ddhd2 DDHD domain containing 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:25267624 1619129 Ddhd2 DDHD domain containing 2 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:25267624 1619129 Ddhd2 DDHD domain containing 2 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20200310 MGI PMID:25267624 1619129 Ddhd2 DDHD domain containing 2 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200310 MGI PMID:25267624 1619130 Dscc1 DNA replication and sister chromatid cohesion 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20160804 MGI 1619130 Dscc1 DNA replication and sister chromatid cohesion 1 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20160804 MGI 1619130 Dscc1 DNA replication and sister chromatid cohesion 1 gene MP:0000480 increased rib number IEA N RGD:5509061 20141003 MGI 1619130 Dscc1 DNA replication and sister chromatid cohesion 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160804 MGI 1619130 Dscc1 DNA replication and sister chromatid cohesion 1 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20141003 MGI 1619130 Dscc1 DNA replication and sister chromatid cohesion 1 gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20141003 MGI 1619130 Dscc1 DNA replication and sister chromatid cohesion 1 gene MP:0004651 increased thoracic vertebrae number IEA N RGD:5509061 20141003 MGI 1619130 Dscc1 DNA replication and sister chromatid cohesion 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1619130 Dscc1 DNA replication and sister chromatid cohesion 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20160804 MGI 1619130 Dscc1 DNA replication and sister chromatid cohesion 1 gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20141003 MGI 1619130 Dscc1 DNA replication and sister chromatid cohesion 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20160804 MGI 1619130 Dscc1 DNA replication and sister chromatid cohesion 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1619131 Aplf aprataxin and PNKP like factor gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:21211721 1619131 Aplf aprataxin and PNKP like factor gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:21211721 1619132 Garin2 golgi associated RAB2 interactor 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1619132 Garin2 golgi associated RAB2 interactor 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1619132 Garin2 golgi associated RAB2 interactor 2 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1619132 Garin2 golgi associated RAB2 interactor 2 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1619132 Garin2 golgi associated RAB2 interactor 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1619132 Garin2 golgi associated RAB2 interactor 2 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1619132 Garin2 golgi associated RAB2 interactor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240425 MGI PMID:37992210 1619132 Garin2 golgi associated RAB2 interactor 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240801 MGI PMID:38935810 1619132 Garin2 golgi associated RAB2 interactor 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240801 MGI PMID:38935810 1619132 Garin2 golgi associated RAB2 interactor 2 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20240801 MGI PMID:38935810 1619134 Ttll7 tubulin tyrosine ligase-like family, member 7 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1619136 Nt5c1b 5'-nucleotidase, cytosolic IB gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1619136 Nt5c1b 5'-nucleotidase, cytosolic IB gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240627 MGI PMID:38835510 1619136 Nt5c1b 5'-nucleotidase, cytosolic IB gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210520 MGI 1619143 Ccdc93 coiled-coil domain containing 93 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20241003 MGI 1619143 Ccdc93 coiled-coil domain containing 93 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20241003 MGI 1619143 Ccdc93 coiled-coil domain containing 93 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20241003 MGI 1619143 Ccdc93 coiled-coil domain containing 93 gene MP:0002582 disorganized extraembryonic tissue IEA N RGD:5509061 20241003 MGI 1619143 Ccdc93 coiled-coil domain containing 93 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20240523 MGI 1619143 Ccdc93 coiled-coil domain containing 93 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20241003 MGI 1619143 Ccdc93 coiled-coil domain containing 93 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1619143 Ccdc93 coiled-coil domain containing 93 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241003 MGI 1619143 Ccdc93 coiled-coil domain containing 93 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1619143 Ccdc93 coiled-coil domain containing 93 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1619143 Ccdc93 coiled-coil domain containing 93 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1619143 Ccdc93 coiled-coil domain containing 93 gene MP:0013504 increased embryonic tissue cell apoptosis IEA N RGD:5509061 20241010 MGI 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20201015 MGI PMID:31004071 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20201015 MGI PMID:31004071 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20201015 MGI PMID:31004071 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0001925 male infertility IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0001925 male infertility IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20201015 MGI PMID:31004071 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0009241 thick sperm flagellum IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20181220 MGI PMID:28552195 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20201015 MGI PMID:31004071 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20201015 MGI PMID:31004071 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0013206 abnormal motile cilium morphology IAGP N RGD:5509061 20201015 MGI PMID:31004071 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20180607 MGI PMID:29449551 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20200227 MGI PMID:29449551 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0031351 abnormal sperm flagellum thickness IAGP N RGD:5509061 20220317 MGI PMID:28552195 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20220317 MGI PMID:28552195 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20220317 MGI PMID:29449551 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220317 MGI PMID:28552195 1619147 Cfap43 cilia and flagella associated protein 43 gene MP:0031438 abnormal sperm radial spoke morphology IAGP N RGD:5509061 20220915 MGI PMID:29449551 1619149 Rhou ras homolog family member U gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1619149 Rhou ras homolog family member U gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20160804 MGI 1619151 Hilpda hypoxia inducible lipid droplet associated gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20230601 MGI 1619151 Hilpda hypoxia inducible lipid droplet associated gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20210805 MGI PMID:28739822 1619151 Hilpda hypoxia inducible lipid droplet associated gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20210805 MGI PMID:28739822 1619151 Hilpda hypoxia inducible lipid droplet associated gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20210805 MGI PMID:28739822 1619151 Hilpda hypoxia inducible lipid droplet associated gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20210805 MGI PMID:28739822 1619151 Hilpda hypoxia inducible lipid droplet associated gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20230601 MGI 1619151 Hilpda hypoxia inducible lipid droplet associated gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20210805 MGI PMID:28739822 1619151 Hilpda hypoxia inducible lipid droplet associated gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20210805 MGI PMID:28739822 1619151 Hilpda hypoxia inducible lipid droplet associated gene MP:0010580 decreased heart left ventricle size IEA N RGD:5509061 20230601 MGI 1619151 Hilpda hypoxia inducible lipid droplet associated gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20210805 MGI PMID:28739822 1619151 Hilpda hypoxia inducible lipid droplet associated gene MP:0011939 increased food intake IAGP N RGD:5509061 20210805 MGI PMID:28739822 1619151 Hilpda hypoxia inducible lipid droplet associated gene MP:0011940 decreased food intake IAGP N RGD:5509061 20210805 MGI PMID:28739822 1619152 Nmrk2 nicotinamide riboside kinase 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1619152 Nmrk2 nicotinamide riboside kinase 2 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1619153 Mrln myoregulin gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20160421 MGI PMID:25640239 1619153 Mrln myoregulin gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20160421 MGI PMID:25640239 1619153 Mrln myoregulin gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20180215 MGI PMID:28091529 1619153 Mrln myoregulin gene MP:0012107 enhanced exercise endurance IAGP N RGD:5509061 20160421 MGI PMID:25640239 1619153 Mrln myoregulin gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20180215 MGI PMID:28091529 1619155 2310022B05Rik RIKEN cDNA 2310022B05 gene gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20141003 MGI 1619155 2310022B05Rik RIKEN cDNA 2310022B05 gene gene MP:0005014 increased B cell number IEA N RGD:5509061 20141003 MGI 1619155 2310022B05Rik RIKEN cDNA 2310022B05 gene gene MP:0010052 increased grip strength IEA N RGD:5509061 20160804 MGI 1619156 Bst2 bone marrow stromal cell antigen 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1619156 Bst2 bone marrow stromal cell antigen 2 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1619156 Bst2 bone marrow stromal cell antigen 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22025715 1619156 Bst2 bone marrow stromal cell antigen 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22025715 1619156 Bst2 bone marrow stromal cell antigen 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1619156 Bst2 bone marrow stromal cell antigen 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1619156 Bst2 bone marrow stromal cell antigen 2 gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 1619156 Bst2 bone marrow stromal cell antigen 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22025715 1619156 Bst2 bone marrow stromal cell antigen 2 gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:22025715 1619158 Nkpd1 NTPase, KAP family P-loop domain containing 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210128 MGI 1619158 Nkpd1 NTPase, KAP family P-loop domain containing 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1619158 Nkpd1 NTPase, KAP family P-loop domain containing 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20240523 MGI 1619161 2300002M23Rik RIKEN cDNA 2300002M23 gene gene MP:0001262 decreased body weight IEA N RGD:5509061 20170323 MGI 1619161 2300002M23Rik RIKEN cDNA 2300002M23 gene gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20170323 MGI 1619164 1700030J22Rik RIKEN cDNA 1700030J22 gene gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1619164 1700030J22Rik RIKEN cDNA 1700030J22 gene gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1619164 1700030J22Rik RIKEN cDNA 1700030J22 gene gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220811 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20210304 MGI PMID:25636339 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0002981 increased liver weight IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0002989 small kidney IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20210304 MGI PMID:25636339 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20210304 MGI PMID:25636339 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0003604 single kidney IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20210304 MGI PMID:25636339 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20210304 MGI PMID:25636339 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20210304 MGI PMID:25636339 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20210304 MGI PMID:25636339 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20240523 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0009454 impaired contextual conditioning behavior IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0009456 impaired cued conditioning behavior IEA N RGD:5509061 20230601 MGI 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20210304 MGI PMID:25636339 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20210304 MGI PMID:25636339 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20210304 MGI PMID:25636339 1619174 Babam1 BRISC and BRCA1 A complex member 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 1619177 Mturn maturin, neural progenitor differentiation regulator homolog (Xenopus) gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20220811 MGI 1619177 Mturn maturin, neural progenitor differentiation regulator homolog (Xenopus) gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20230601 MGI 1619177 Mturn maturin, neural progenitor differentiation regulator homolog (Xenopus) gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150430 MGI 1619177 Mturn maturin, neural progenitor differentiation regulator homolog (Xenopus) gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1619177 Mturn maturin, neural progenitor differentiation regulator homolog (Xenopus) gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20150430 MGI 1619179 H2al2a H2A histone family member L2A gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1619179 H2al2a H2A histone family member L2A gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20201231 MGI 1619180 Spindoc spindlin interactor and repressor of chromatin binding gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230601 MGI PMID:34737271 1619180 Spindoc spindlin interactor and repressor of chromatin binding gene MP:0002879 increased cellular sensitivity to X-ray irradiation IAGP N RGD:5509061 20230601 MGI PMID:34737271 1619180 Spindoc spindlin interactor and repressor of chromatin binding gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20230601 MGI PMID:34737271 1619180 Spindoc spindlin interactor and repressor of chromatin binding gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20230601 MGI PMID:34737271 1619186 Diras2 DIRAS family, GTP-binding RAS-like 2 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20241031 MGI PMID:38574733 1619186 Diras2 DIRAS family, GTP-binding RAS-like 2 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20241031 MGI PMID:38574733 1619187 Ccdc34 coiled-coil domain containing 34 gene MP:0001925 male infertility IAGP N RGD:5509061 20230323 MGI PMID:34348960 1619187 Ccdc34 coiled-coil domain containing 34 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230323 MGI PMID:34348960 1619187 Ccdc34 coiled-coil domain containing 34 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230323 MGI PMID:34348960 1619187 Ccdc34 coiled-coil domain containing 34 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230323 MGI PMID:34348960 1619187 Ccdc34 coiled-coil domain containing 34 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20220811 MGI 1619187 Ccdc34 coiled-coil domain containing 34 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20230323 MGI PMID:34348960 1619187 Ccdc34 coiled-coil domain containing 34 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20230323 MGI PMID:34348960 1619187 Ccdc34 coiled-coil domain containing 34 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20230323 MGI PMID:34348960 1619188 Med28 mediator complex subunit 28 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200310 MGI 1619188 Med28 mediator complex subunit 28 gene MP:0000692 small spleen IEA N RGD:5509061 20200310 MGI 1619188 Med28 mediator complex subunit 28 gene MP:0001257 increased body length IEA N RGD:5509061 20201022 MGI 1619188 Med28 mediator complex subunit 28 gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20200310 MGI PMID:26445504 1619188 Med28 mediator complex subunit 28 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200310 MGI 1619188 Med28 mediator complex subunit 28 gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20200310 MGI PMID:26445504 1619188 Med28 mediator complex subunit 28 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20200310 MGI PMID:26445504 1619188 Med28 mediator complex subunit 28 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1619188 Med28 mediator complex subunit 28 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20200310 MGI PMID:26445504 1619188 Med28 mediator complex subunit 28 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1619188 Med28 mediator complex subunit 28 gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20231207 MGI 1619188 Med28 mediator complex subunit 28 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:26445504 1619188 Med28 mediator complex subunit 28 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619188 Med28 mediator complex subunit 28 gene MP:0011184 absent embryonic epiblast IAGP N RGD:5509061 20200310 MGI PMID:26445504 1619188 Med28 mediator complex subunit 28 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20200310 MGI PMID:26445504 1619188 Med28 mediator complex subunit 28 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1619188 Med28 mediator complex subunit 28 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1619189 Ceacam11 CEA cell adhesion molecule 11 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1619192 Edem3 ER degradation enhancer, mannosidase alpha-like 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1619192 Edem3 ER degradation enhancer, mannosidase alpha-like 3 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1619192 Edem3 ER degradation enhancer, mannosidase alpha-like 3 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1619192 Edem3 ER degradation enhancer, mannosidase alpha-like 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20190808 MGI 1619192 Edem3 ER degradation enhancer, mannosidase alpha-like 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20190808 MGI 1619192 Edem3 ER degradation enhancer, mannosidase alpha-like 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619193 Pacc1 proton activated chloride channel 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20190926 MGI PMID:31023925 1619193 Pacc1 proton activated chloride channel 1 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20190926 MGI PMID:31023925 1619193 Pacc1 proton activated chloride channel 1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20190926 MGI PMID:31023925 1619193 Pacc1 proton activated chloride channel 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20190926 MGI PMID:31023925 1619194 Shisa5 shisa family member 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17481602 1619197 Rexo1 REX1, RNA exonuclease 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1619197 Rexo1 REX1, RNA exonuclease 1 gene MP:0000603 pale liver IEA N RGD:5509061 20210826 MGI 1619197 Rexo1 REX1, RNA exonuclease 1 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20210826 MGI 1619197 Rexo1 REX1, RNA exonuclease 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210826 MGI 1619197 Rexo1 REX1, RNA exonuclease 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1619197 Rexo1 REX1, RNA exonuclease 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210826 MGI 1619197 Rexo1 REX1, RNA exonuclease 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210826 MGI 1619197 Rexo1 REX1, RNA exonuclease 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20220519 MGI 1619197 Rexo1 REX1, RNA exonuclease 1 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20220519 MGI 1619197 Rexo1 REX1, RNA exonuclease 1 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20220519 MGI 1619197 Rexo1 REX1, RNA exonuclease 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210826 MGI 1619197 Rexo1 REX1, RNA exonuclease 1 gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20210826 MGI 1619197 Rexo1 REX1, RNA exonuclease 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1619197 Rexo1 REX1, RNA exonuclease 1 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20220519 MGI 1619198 1700010I14Rik RIKEN cDNA 1700010I14 gene gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20231012 MGI PMID:36598146 1619198 1700010I14Rik RIKEN cDNA 1700010I14 gene gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 1619198 1700010I14Rik RIKEN cDNA 1700010I14 gene gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20231012 MGI PMID:36598146 1619198 1700010I14Rik RIKEN cDNA 1700010I14 gene gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20231012 MGI PMID:36598146 1619198 1700010I14Rik RIKEN cDNA 1700010I14 gene gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1619199 Cops9 COP9 signalosome subunit 9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1619200 Tmem107 transmembrane protein 107 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0000080 abnormal exoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0000088 short mandible IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0000105 impaired ossification of basisphenoid bone IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0000445 short snout IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0000568 ectopic digits IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0000914 exencephaly IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0002243 abnormal vomeronasal organ morphology IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0004451 short presphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0004468 small zygomatic bone IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0004540 small maxilla IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0004574 broad limb buds IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0009897 decreased maxillary shelf size IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 1619200 Tmem107 transmembrane protein 107 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0011505 camptomelia IAGP N RGD:5509061 20141003 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:22698544 1619200 Tmem107 transmembrane protein 107 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0021217 abnormal palatal shelf bone ossification IAGP N RGD:5509061 20230302 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0030189 broad snout IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0030200 abnormal nasal septum cartilage morphology IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0030204 large nasal septum IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0030205 thick nasal septum IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0030467 abnormal cranial cartilage development IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0031447 unilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0031457 abnormal vomeronasal cartilage morphology IAGP N RGD:5509061 20221124 MGI PMID:28954202 1619200 Tmem107 transmembrane protein 107 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:28954202 1619201 Fndc4 fibronectin type III domain containing 4 gene MP:0001263 weight loss IAGP N RGD:5509061 20180111 MGI PMID:27066907 1619201 Fndc4 fibronectin type III domain containing 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1619201 Fndc4 fibronectin type III domain containing 4 gene MP:0001513 limb grasping IEA N RGD:5509061 20181227 MGI 1619201 Fndc4 fibronectin type III domain containing 4 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1619201 Fndc4 fibronectin type III domain containing 4 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20180111 MGI PMID:27066907 1619201 Fndc4 fibronectin type III domain containing 4 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1619201 Fndc4 fibronectin type III domain containing 4 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20180111 MGI PMID:27066907 1619204 Sap30 sin3 associated polypeptide gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1619204 Sap30 sin3 associated polypeptide gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1619204 Sap30 sin3 associated polypeptide gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1619204 Sap30 sin3 associated polypeptide gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1619204 Sap30 sin3 associated polypeptide gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220519 MGI 1619206 Il17re interleukin 17 receptor E gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:21993848 1619206 Il17re interleukin 17 receptor E gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21993849 1619206 Il17re interleukin 17 receptor E gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21993848 1619206 Il17re interleukin 17 receptor E gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21993848 1619206 Il17re interleukin 17 receptor E gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:21993848 1619206 Il17re interleukin 17 receptor E gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:21993848 1619206 Il17re interleukin 17 receptor E gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21993849 1619206 Il17re interleukin 17 receptor E gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:21993848 1619207 Hacd3 3-hydroxyacyl-CoA dehydratase 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 1619207 Hacd3 3-hydroxyacyl-CoA dehydratase 3 gene MP:0000599 enlarged liver IEA N RGD:5509061 20210826 MGI 1619207 Hacd3 3-hydroxyacyl-CoA dehydratase 3 gene MP:0000601 small liver IEA N RGD:5509061 20220811 MGI 1619207 Hacd3 3-hydroxyacyl-CoA dehydratase 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1619207 Hacd3 3-hydroxyacyl-CoA dehydratase 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1619207 Hacd3 3-hydroxyacyl-CoA dehydratase 3 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1619207 Hacd3 3-hydroxyacyl-CoA dehydratase 3 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210826 MGI 1619207 Hacd3 3-hydroxyacyl-CoA dehydratase 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1619207 Hacd3 3-hydroxyacyl-CoA dehydratase 3 gene MP:0001304 cataract IEA N RGD:5509061 20210128 MGI 1619207 Hacd3 3-hydroxyacyl-CoA dehydratase 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1619207 Hacd3 3-hydroxyacyl-CoA dehydratase 3 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210128 MGI 1619207 Hacd3 3-hydroxyacyl-CoA dehydratase 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1619207 Hacd3 3-hydroxyacyl-CoA dehydratase 3 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1619207 Hacd3 3-hydroxyacyl-CoA dehydratase 3 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20231207 MGI 1619207 Hacd3 3-hydroxyacyl-CoA dehydratase 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1619208 Raet1d retinoic acid early transcript delta gene MP:0003080 increased natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20160630 MGI PMID:25745066 1619209 Vmn2r26 vomeronasal 2, receptor 26 gene MP:0004513 avnosmia IAGP N RGD:5509061 20170406 MGI PMID:19935653 1619209 Vmn2r26 vomeronasal 2, receptor 26 gene MP:0011678 abnormal vomeronasal sensory neuron physiology IAGP N RGD:5509061 20170406 MGI PMID:19935653 1619210 Vmn2r1 vomeronasal 2, receptor 1 gene MP:0002243 abnormal vomeronasal organ morphology IAGP N RGD:5509061 20180628 MGI PMID:29465786 1619210 Vmn2r1 vomeronasal 2, receptor 1 gene MP:0011679 abnormal vomeronasal sensory neuron morphology IAGP N RGD:5509061 20180628 MGI PMID:29465786 1619211 Ylpm1 YLP motif containing 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20181227 MGI 1619211 Ylpm1 YLP motif containing 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1619211 Ylpm1 YLP motif containing 1 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191128 MGI 1619211 Ylpm1 YLP motif containing 1 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191128 MGI 1619211 Ylpm1 YLP motif containing 1 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191128 MGI 1619211 Ylpm1 YLP motif containing 1 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1619211 Ylpm1 YLP motif containing 1 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191128 MGI 1619211 Ylpm1 YLP motif containing 1 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191128 MGI 1619211 Ylpm1 YLP motif containing 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20221215 MGI 1619211 Ylpm1 YLP motif containing 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1619211 Ylpm1 YLP motif containing 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1619211 Ylpm1 YLP motif containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619211 Ylpm1 YLP motif containing 1 gene MP:0012724 absent head fold IEA N RGD:5509061 20191128 MGI 1619211 Ylpm1 YLP motif containing 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20221215 MGI 1619211 Ylpm1 YLP motif containing 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191128 MGI 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20201231 MGI 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20201022 MGI 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20201022 MGI 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0001147 small testis IEA N RGD:5509061 20201022 MGI 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190926 MGI PMID:28869608 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20201022 MGI 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20190926 MGI PMID:28869608 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20190926 MGI PMID:28869608 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20201022 MGI 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20190926 MGI PMID:28869608 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20190926 MGI PMID:28869608 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20190926 MGI PMID:28869608 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20190926 MGI PMID:28869608 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20211021 MGI 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:28869608 1619212 Cnpy2 canopy FGF signaling regulator 2 gene MP:0031601 decreased endoplasmic reticulum stress IAGP N RGD:5509061 20240418 MGI PMID:28869608 1619213 Zfp235 zinc finger protein 235 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20210128 MGI 1619213 Zfp235 zinc finger protein 235 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20201022 MGI 1619213 Zfp235 zinc finger protein 235 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1619214 Slc22a21 solute carrier family 22 (organic cation transporter), member 21 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160915 MGI PMID:24652767 1619214 Slc22a21 solute carrier family 22 (organic cation transporter), member 21 gene MP:0009199 abnormal external male genitalia morphology IEA N RGD:5509061 20160804 MGI 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20180830 MGI PMID:27737959 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17640884 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20160204 MGI PMID:25474630 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20180830 MGI PMID:27737959 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180830 MGI PMID:27737959 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17640884 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20180830 MGI PMID:27737959 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17640884 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17640884 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20160204 MGI PMID:25474630 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20160204 MGI PMID:25474630 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20180830 MGI PMID:27737959 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17640884 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17640884 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17640884 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20160204 MGI PMID:25474630 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17640884 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17640884 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20160204 MGI PMID:25474630 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20160804 MGI 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:17640884 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:17640884 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0008830 abnormal nucleolus morphology IAGP N RGD:5509061 20160204 MGI PMID:25474630 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20160204 MGI PMID:25474630 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:17640884 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160204 MGI PMID:25474630 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20160204 MGI PMID:25474630 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0012204 abnormal neuronal stem cell physiology IAGP N RGD:5509061 20160204 MGI PMID:25474630 1619218 Ncaph2 non-SMC condensin II complex, subunit H2 gene MP:0020066 abnormal neocortex size IAGP N RGD:5509061 20180830 MGI PMID:27737959 1619220 Arhgef25 Rho guanine nucleotide exchange factor 25 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22449701 1619222 Esyt2 extended synaptotagmin-like protein 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20190502 MGI 1619222 Esyt2 extended synaptotagmin-like protein 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20150528 MGI 1619222 Esyt2 extended synaptotagmin-like protein 2 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20170518 MGI PMID:25486202 1619222 Esyt2 extended synaptotagmin-like protein 2 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20170518 MGI PMID:25486202 1619222 Esyt2 extended synaptotagmin-like protein 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170518 MGI PMID:25486202 1619222 Esyt2 extended synaptotagmin-like protein 2 gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20170518 MGI PMID:25486202 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:21059868 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18416604 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18416604 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:18416604 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15385962 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:21059868 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:19535498 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0000777 increased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:19535498 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:19535498 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19535498 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:19535498 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:19535498 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:19535498 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0000905 increased superior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:19535498 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:19535498 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15385962 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16687444 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18416604 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15385962 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:19535498 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0002083 premature death IAGP N RGD:5509061 20160107 MGI PMID:25119042 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:15385962 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15385962 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16687444 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:19535498 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18416604 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:15385962 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20160107 MGI PMID:25119042 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:21059868 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:19535498 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18416604 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15385962 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:21059868 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:21059868 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:21059868 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18416604 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:15385962 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:18416604 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0009048 enlarged tectum IAGP N RGD:5509061 20141003 MGI PMID:19535498 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0010310 increased Schwannoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0010314 increased neurofibroma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18416604 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15385962 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16687444 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21059868 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19535498 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18416604 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:15385962 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0011200 abnormal extraembryonic coelom morphology IAGP N RGD:5509061 20141003 MGI PMID:15385962 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0011202 abnormal ectoplacental cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:15385962 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160107 MGI PMID:25119042 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0012710 diastematomyelia IAGP N RGD:5509061 20141003 MGI PMID:19535498 1619223 Suz12 SUZ12 polycomb repressive complex 2 subunit gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:15385962 1619226 Taf7 TATA-box binding protein associated factor 7 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:22411629 1619226 Taf7 TATA-box binding protein associated factor 7 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22411629 1619226 Taf7 TATA-box binding protein associated factor 7 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:22411629 1619226 Taf7 TATA-box binding protein associated factor 7 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22411629 1619226 Taf7 TATA-box binding protein associated factor 7 gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:22411629 1619226 Taf7 TATA-box binding protein associated factor 7 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22411629 1619226 Taf7 TATA-box binding protein associated factor 7 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:22411629 1619226 Taf7 TATA-box binding protein associated factor 7 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22411629 1619226 Taf7 TATA-box binding protein associated factor 7 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22411629 1619226 Taf7 TATA-box binding protein associated factor 7 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22411629 1619226 Taf7 TATA-box binding protein associated factor 7 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22411629 1619226 Taf7 TATA-box binding protein associated factor 7 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22411629 1619226 Taf7 TATA-box binding protein associated factor 7 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22411629 1619228 Rnf13 ring finger protein 13 gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20240523 MGI 1619228 Rnf13 ring finger protein 13 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20240822 MGI PMID:22890573 1619228 Rnf13 ring finger protein 13 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20240822 MGI PMID:22890573 1619228 Rnf13 ring finger protein 13 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1619228 Rnf13 ring finger protein 13 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20240822 MGI PMID:22890573 1619228 Rnf13 ring finger protein 13 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20201231 MGI 1619228 Rnf13 ring finger protein 13 gene MP:0012000 abnormal limb position IEA N RGD:5509061 20240523 MGI 1619228 Rnf13 ring finger protein 13 gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240822 MGI PMID:22890573 1619228 Rnf13 ring finger protein 13 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20240822 MGI PMID:22890573 1619229 Rai2 retinoic acid induced 2 gene MP:0002764 short tibia IEA N RGD:5509061 20220519 MGI 1619229 Rai2 retinoic acid induced 2 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20221215 MGI 1619234 Zfp90 zinc finger protein 90 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1619240 Tcra T cell receptor alpha chain gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:18242214 1619240 Tcra T cell receptor alpha chain gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20141003 MGI PMID:8104709 1619240 Tcra T cell receptor alpha chain gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:18242214 1619240 Tcra T cell receptor alpha chain gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:8104709 1619240 Tcra T cell receptor alpha chain gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:9006326 1619240 Tcra T cell receptor alpha chain gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:9006326 1619240 Tcra T cell receptor alpha chain gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:9006326 1619240 Tcra T cell receptor alpha chain gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:8104709 1619240 Tcra T cell receptor alpha chain gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17785826 1619240 Tcra T cell receptor alpha chain gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7991563 1619240 Tcra T cell receptor alpha chain gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7991563 1619240 Tcra T cell receptor alpha chain gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17785826 1619240 Tcra T cell receptor alpha chain gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:18203137 1619240 Tcra T cell receptor alpha chain gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23853545 1619240 Tcra T cell receptor alpha chain gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:9036998 1619240 Tcra T cell receptor alpha chain gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15964276 1619240 Tcra T cell receptor alpha chain gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:9036998 1619240 Tcra T cell receptor alpha chain gene MP:0001665 chronic diarrhea IAGP N RGD:5509061 20141003 MGI PMID:8104709 1619240 Tcra T cell receptor alpha chain gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16272283 1619240 Tcra T cell receptor alpha chain gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:1359428 1619240 Tcra T cell receptor alpha chain gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17617584 1619240 Tcra T cell receptor alpha chain gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17998389 1619240 Tcra T cell receptor alpha chain gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:1359428 1619240 Tcra T cell receptor alpha chain gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17442925 1619240 Tcra T cell receptor alpha chain gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23853545 1619240 Tcra T cell receptor alpha chain gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:7991563 1619240 Tcra T cell receptor alpha chain gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:8208291 1619240 Tcra T cell receptor alpha chain gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:9892615 1619240 Tcra T cell receptor alpha chain gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22284419 1619240 Tcra T cell receptor alpha chain gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:9472669 1619240 Tcra T cell receptor alpha chain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19004778 1619240 Tcra T cell receptor alpha chain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8104709 1619240 Tcra T cell receptor alpha chain gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:16272283 1619240 Tcra T cell receptor alpha chain gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:9036998 1619240 Tcra T cell receptor alpha chain gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:9472669 1619240 Tcra T cell receptor alpha chain gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12049722 1619240 Tcra T cell receptor alpha chain gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17617584 1619240 Tcra T cell receptor alpha chain gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18203137 1619240 Tcra T cell receptor alpha chain gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:1604321 1619240 Tcra T cell receptor alpha chain gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17617584 1619240 Tcra T cell receptor alpha chain gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18203137 1619240 Tcra T cell receptor alpha chain gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12049722 1619240 Tcra T cell receptor alpha chain gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12383644 1619240 Tcra T cell receptor alpha chain gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11447257 1619240 Tcra T cell receptor alpha chain gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23853545 1619240 Tcra T cell receptor alpha chain gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7561698 1619240 Tcra T cell receptor alpha chain gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9036998 1619240 Tcra T cell receptor alpha chain gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:8208291 1619240 Tcra T cell receptor alpha chain gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:8208291 1619240 Tcra T cell receptor alpha chain gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:1604321 1619240 Tcra T cell receptor alpha chain gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:18242214 1619240 Tcra T cell receptor alpha chain gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:19004778 1619240 Tcra T cell receptor alpha chain gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:22284419 1619240 Tcra T cell receptor alpha chain gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:8104709 1619240 Tcra T cell receptor alpha chain gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:9006326 1619240 Tcra T cell receptor alpha chain gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10632602 1619240 Tcra T cell receptor alpha chain gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:9472669 1619240 Tcra T cell receptor alpha chain gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17785826 1619240 Tcra T cell receptor alpha chain gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8104709 1619240 Tcra T cell receptor alpha chain gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:10632602 1619240 Tcra T cell receptor alpha chain gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:8208291 1619240 Tcra T cell receptor alpha chain gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:9036998 1619240 Tcra T cell receptor alpha chain gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:18242214 1619240 Tcra T cell receptor alpha chain gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:10632602 1619240 Tcra T cell receptor alpha chain gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:17785826 1619240 Tcra T cell receptor alpha chain gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:22284419 1619240 Tcra T cell receptor alpha chain gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:8208291 1619240 Tcra T cell receptor alpha chain gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:9036998 1619240 Tcra T cell receptor alpha chain gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:8208291 1619240 Tcra T cell receptor alpha chain gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:7561698 1619240 Tcra T cell receptor alpha chain gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:12049722 1619240 Tcra T cell receptor alpha chain gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:17998389 1619240 Tcra T cell receptor alpha chain gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:23853545 1619240 Tcra T cell receptor alpha chain gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:22284419 1619240 Tcra T cell receptor alpha chain gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11447257 1619240 Tcra T cell receptor alpha chain gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8208291 1619240 Tcra T cell receptor alpha chain gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23853545 1619240 Tcra T cell receptor alpha chain gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:7540652 1619240 Tcra T cell receptor alpha chain gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:7991563 1619240 Tcra T cell receptor alpha chain gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10632602 1619240 Tcra T cell receptor alpha chain gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:16272283 1619240 Tcra T cell receptor alpha chain gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:9006326 1619240 Tcra T cell receptor alpha chain gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:23853545 1619240 Tcra T cell receptor alpha chain gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:9751751 1619240 Tcra T cell receptor alpha chain gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:1359428 1619240 Tcra T cell receptor alpha chain gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17617584 1619240 Tcra T cell receptor alpha chain gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17998389 1619240 Tcra T cell receptor alpha chain gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18203137 1619240 Tcra T cell receptor alpha chain gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22653054 1619240 Tcra T cell receptor alpha chain gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18155708 1619240 Tcra T cell receptor alpha chain gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7991563 1619240 Tcra T cell receptor alpha chain gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:9472669 1619240 Tcra T cell receptor alpha chain gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:10632602 1619240 Tcra T cell receptor alpha chain gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:9472669 1619240 Tcra T cell receptor alpha chain gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:14525595 1619240 Tcra T cell receptor alpha chain gene MP:0008036 abnormal NK T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15975513 1619240 Tcra T cell receptor alpha chain gene MP:0008036 abnormal NK T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17785826 1619240 Tcra T cell receptor alpha chain gene MP:0008036 abnormal NK T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23853545 1619240 Tcra T cell receptor alpha chain gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11447257 1619240 Tcra T cell receptor alpha chain gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12049715 1619240 Tcra T cell receptor alpha chain gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15964276 1619240 Tcra T cell receptor alpha chain gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1604321 1619240 Tcra T cell receptor alpha chain gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:17785826 1619240 Tcra T cell receptor alpha chain gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:23853545 1619240 Tcra T cell receptor alpha chain gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:23853545 1619240 Tcra T cell receptor alpha chain gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15975513 1619240 Tcra T cell receptor alpha chain gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:23853545 1619240 Tcra T cell receptor alpha chain gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:15004164 1619240 Tcra T cell receptor alpha chain gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1359428 1619240 Tcra T cell receptor alpha chain gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17617584 1619240 Tcra T cell receptor alpha chain gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17617584 1619240 Tcra T cell receptor alpha chain gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1359428 1619240 Tcra T cell receptor alpha chain gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:1604321 1619240 Tcra T cell receptor alpha chain gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:7540652 1619240 Tcra T cell receptor alpha chain gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:7991563 1619240 Tcra T cell receptor alpha chain gene MP:0008348 absent gamma-delta T cells IAGP N RGD:5509061 20141003 MGI PMID:17617584 1619240 Tcra T cell receptor alpha chain gene MP:0008348 absent gamma-delta T cells IAGP N RGD:5509061 20141003 MGI PMID:18242214 1619240 Tcra T cell receptor alpha chain gene MP:0008350 increased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:7540652 1619240 Tcra T cell receptor alpha chain gene MP:0008350 increased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:8104709 1619240 Tcra T cell receptor alpha chain gene MP:0008353 increased mature gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18242214 1619240 Tcra T cell receptor alpha chain gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19004778 1619240 Tcra T cell receptor alpha chain gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7991563 1619240 Tcra T cell receptor alpha chain gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:17785826 1619240 Tcra T cell receptor alpha chain gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:17785826 1619240 Tcra T cell receptor alpha chain gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:8208291 1619240 Tcra T cell receptor alpha chain gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17785826 1619240 Tcra T cell receptor alpha chain gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:17785826 1619240 Tcra T cell receptor alpha chain gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17785826 1619240 Tcra T cell receptor alpha chain gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:17785826 1619240 Tcra T cell receptor alpha chain gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19004778 1619240 Tcra T cell receptor alpha chain gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:18155708 1619240 Tcra T cell receptor alpha chain gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18242214 1619240 Tcra T cell receptor alpha chain gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:10632602 1619240 Tcra T cell receptor alpha chain gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:1604321 1619240 Tcra T cell receptor alpha chain gene MP:0008895 abnormal intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:19004778 1619240 Tcra T cell receptor alpha chain gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:17785826 1619240 Tcra T cell receptor alpha chain gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:21179499 1619240 Tcra T cell receptor alpha chain gene MP:0010742 increased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:10632602 1619240 Tcra T cell receptor alpha chain gene MP:0010833 abnormal memory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11447257 1619240 Tcra T cell receptor alpha chain gene MP:0013587 absent thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:1604321 1619240 Tcra T cell receptor alpha chain gene MP:0013593 enlarged thymus cortex IAGP N RGD:5509061 20150319 MGI PMID:1604321 1619244 Mlx MAX-like protein X gene MP:0001759 increased urine glucose level IEA N RGD:5509061 20240523 MGI 1619244 Mlx MAX-like protein X gene MP:0001925 male infertility IAGP N RGD:5509061 20230330 MGI PMID:34669700 1619244 Mlx MAX-like protein X gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20230330 MGI PMID:34669700 1619244 Mlx MAX-like protein X gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220519 MGI 1619244 Mlx MAX-like protein X gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230330 MGI PMID:34669700 1619244 Mlx MAX-like protein X gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230330 MGI PMID:34669700 1619244 Mlx MAX-like protein X gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1619244 Mlx MAX-like protein X gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230330 MGI PMID:34669700 1619244 Mlx MAX-like protein X gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20230330 MGI PMID:34669700 1619244 Mlx MAX-like protein X gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20230330 MGI PMID:34669700 1619244 Mlx MAX-like protein X gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1619244 Mlx MAX-like protein X gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1619244 Mlx MAX-like protein X gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230330 MGI PMID:34669700 1619244 Mlx MAX-like protein X gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20230601 MGI 1619244 Mlx MAX-like protein X gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20211021 MGI 1619244 Mlx MAX-like protein X gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1619244 Mlx MAX-like protein X gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20230330 MGI PMID:26584623 1619244 Mlx MAX-like protein X gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1619244 Mlx MAX-like protein X gene MP:0020450 abnormal sperm progressive motility IAGP N RGD:5509061 20230330 MGI PMID:34669700 1619245 Vps72 vacuolar protein sorting 72 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:13943454 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:16578176 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:2379821 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0000692 small spleen IEA N RGD:5509061 20220519 MGI 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0000706 small thymus IEA N RGD:5509061 20220519 MGI 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12548288 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16578176 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4634048 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:102659 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220519 MGI 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:6776948 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0002546 mydriasis IEA N RGD:5509061 20201022 MGI 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0003171 phenotypic reversion IAGP N RGD:5509061 20141003 MGI PMID:2379821 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0004165 abnormal lateral geniculate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:102659 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:2369371 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:6696991 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0005077 abnormal melanogenesis IAGP N RGD:5509061 20141003 MGI PMID:4634048 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0005100 abnormal choroid pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12548288 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16578176 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:13943454 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16578176 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:2369371 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:17247639 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:6696991 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:102659 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0008763 abnormal mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:8962054 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20141003 MGI PMID:6696991 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0009557 decreased platelet ADP level IAGP N RGD:5509061 20141003 MGI PMID:6696991 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0010192 abnormal retina melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0011279 decreased ear pigmentation IEA N RGD:5509061 20170803 MGI 1619246 Hps6 HPS6, biogenesis of lysosomal organelles complex 2 subunit 3 gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170720 MGI PMID:6696991 1619248 Trim30a tripartite motif-containing 30A gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141225 MGI PMID:24756037 1619248 Trim30a tripartite motif-containing 30A gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141225 MGI PMID:24756037 1619248 Trim30a tripartite motif-containing 30A gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141225 MGI PMID:24756037 1619248 Trim30a tripartite motif-containing 30A gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141225 MGI PMID:24756037 1619249 Pmp2 peripheral myelin protein 2 gene MP:0000745 tremors IAGP N RGD:5509061 20161027 MGI PMID:24849898 1619249 Pmp2 peripheral myelin protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20161027 MGI PMID:24849898 1619249 Pmp2 peripheral myelin protein 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20161027 MGI PMID:24849898 1619249 Pmp2 peripheral myelin protein 2 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20161027 MGI PMID:24849898 1619249 Pmp2 peripheral myelin protein 2 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20161027 MGI PMID:24849898 1619252 Prl2c2 prolactin family 2, subfamily c, member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:22516201 1619252 Prl2c2 prolactin family 2, subfamily c, member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:29967292 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0000031 abnormal cochlea morphology IEA N RGD:5509061 20111116 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0000043 organ of Corti degeneration IEA N RGD:5509061 20111116 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:10673153 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:10233845 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:10673153 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10820170 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7564095 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:10673153 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10233845 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002833 increased heart weight IEA N RGD:5509061 20201022 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002857 cochlear ganglion degeneration IEA N RGD:5509061 20111116 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:10233845 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:10820170 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:10233845 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:10673153 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0003169 abnormal scala media morphology IEA N RGD:5509061 20111116 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0003606 kidney failure IEA N RGD:5509061 20111116 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0003637 cochlear ganglion hypoplasia IEA N RGD:5509061 20111116 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:10820170 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0004363 stria vascularis degeneration IEA N RGD:5509061 20111116 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0004404 cochlear outer hair cell degeneration IEA N RGD:5509061 20111116 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20141003 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0004740 sensorineural hearing loss IEA N RGD:5509061 20111116 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0004864 spiral ligament degeneration IEA N RGD:5509061 20111116 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:10233845 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:10820170 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0005502 abnormal renal/urinary system physiology IAGP N RGD:5509061 20141003 MGI PMID:10673153 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:10673153 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:10233845 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0008987 abnormal liver lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0008993 abnormal portal triad morphology IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0011157 abnormal hypodermis muscle layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10233845 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:1696177 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:10233845 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20141003 MGI 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0012725 small sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20201001 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0014386 decreased muscle fiber mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:18818194 1619253 Mpv17 MpV17 mitochondrial inner membrane protein gene MP:0014388 decreased hepatocyte mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:18818194 1619254 Mpp1 membrane protein, palmitoylated gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19897731 1619254 Mpp1 membrane protein, palmitoylated gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:19897731 1619254 Mpp1 membrane protein, palmitoylated gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:19897731 1619255 Impact impact, RWD domain protein gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20240523 MGI 1619255 Impact impact, RWD domain protein gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20240523 MGI 1619255 Impact impact, RWD domain protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210527 MGI PMID:31166980 1619255 Impact impact, RWD domain protein gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1619255 Impact impact, RWD domain protein gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20210527 MGI PMID:31166980 1619255 Impact impact, RWD domain protein gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20240523 MGI 1619255 Impact impact, RWD domain protein gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20210527 MGI PMID:31166980 1619255 Impact impact, RWD domain protein gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20240523 MGI 1619255 Impact impact, RWD domain protein gene MP:0004156 abnormal QT variability IEA N RGD:5509061 20240523 MGI 1619255 Impact impact, RWD domain protein gene MP:0004882 enlarged lung IEA N RGD:5509061 20240523 MGI 1619255 Impact impact, RWD domain protein gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20210527 MGI PMID:31166980 1619255 Impact impact, RWD domain protein gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20240523 MGI 1619255 Impact impact, RWD domain protein gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20210527 MGI PMID:31166980 1619255 Impact impact, RWD domain protein gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20210527 MGI PMID:31166980 1619255 Impact impact, RWD domain protein gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20240523 MGI 1619255 Impact impact, RWD domain protein gene MP:0011940 decreased food intake IAGP N RGD:5509061 20210527 MGI PMID:31166980 1619255 Impact impact, RWD domain protein gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20210527 MGI PMID:31166980 1619255 Impact impact, RWD domain protein gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:20194894 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0002491 decreased IgD level IEA N RGD:5509061 20200310 MGI 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0002494 increased IgM level IEA N RGD:5509061 20200310 MGI 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:20194894 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0004978 decreased B-1 B cell number IEA N RGD:5509061 20200310 MGI 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:20194894 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:20194894 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:20194894 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:20194894 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:20194894 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:20194894 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20200310 MGI PMID:20194894 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0008170 decreased B-1b cell number IAGP N RGD:5509061 20200310 MGI PMID:20194894 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20200310 MGI PMID:20194894 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20200310 MGI PMID:20194894 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20200310 MGI PMID:20194894 1619256 Gimap1 GTPase, IMAP family member 1 gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20200310 MGI PMID:20194894 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:10499926 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:15728484 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20180315 MGI PMID:29472249 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:15728484 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20180315 MGI PMID:29472249 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180111 MGI PMID:21964024 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:19346486 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:19346486 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:19346486 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:19346486 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20180315 MGI PMID:29472249 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0004031 insulitis IAGP N RGD:5509061 20180315 MGI PMID:29472249 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20171214 MGI PMID:21964024 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20180315 MGI PMID:29472249 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20180315 MGI PMID:29472249 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16476767 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10229092 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180322 MGI PMID:29472249 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10229092 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9182675 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20180913 MGI PMID:28923946 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0012765 decreased alpha-beta T cell number IAGP N RGD:5509061 20180322 MGI PMID:29472249 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0030987 spinal cord inflammation IAGP N RGD:5509061 20191128 MGI PMID:15728484 1619267 H2-D1 histocompatibility 2, D region locus 1 gene MP:0031023 decreased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:10229092 1619269 H2-Aa histocompatibility 2, class II antigen A, alpha gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:8398989 1619269 H2-Aa histocompatibility 2, class II antigen A, alpha gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:8398989 1619269 H2-Aa histocompatibility 2, class II antigen A, alpha gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20200310 MGI PMID:8398989 1619269 H2-Aa histocompatibility 2, class II antigen A, alpha gene MP:0005040 abnormal MHC II cell surface expression on macrophages IAGP N RGD:5509061 20200310 MGI PMID:10621974 1619269 H2-Aa histocompatibility 2, class II antigen A, alpha gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:8398989 1619269 H2-Aa histocompatibility 2, class II antigen A, alpha gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:8398989 1619269 H2-Aa histocompatibility 2, class II antigen A, alpha gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:8398989 1619269 H2-Aa histocompatibility 2, class II antigen A, alpha gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:8398989 1619274 Gypa glycophorin A gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12940824 1619275 Magi1 membrane associated guanylate kinase, WW and PDZ domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:27707879 1619275 Magi1 membrane associated guanylate kinase, WW and PDZ domain containing 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20200310 MGI PMID:27707879 1619275 Magi1 membrane associated guanylate kinase, WW and PDZ domain containing 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20200310 MGI PMID:27707879 1619275 Magi1 membrane associated guanylate kinase, WW and PDZ domain containing 1 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:27707879 1619275 Magi1 membrane associated guanylate kinase, WW and PDZ domain containing 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20200310 MGI PMID:30944250 1619275 Magi1 membrane associated guanylate kinase, WW and PDZ domain containing 1 gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20200310 MGI PMID:27707879 1619275 Magi1 membrane associated guanylate kinase, WW and PDZ domain containing 1 gene MP:0011131 abnormal lung endothelial cell physiology IAGP N RGD:5509061 20200310 MGI PMID:30944250 1619275 Magi1 membrane associated guanylate kinase, WW and PDZ domain containing 1 gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20200310 MGI PMID:27707879 1619277 Ehd1 EH-domain containing 1 gene MP:0000120 malocclusion IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0002208 abnormal germ cell morphology IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20200310 MGI 1619277 Ehd1 EH-domain containing 1 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20200310 MGI PMID:17284518 1619277 Ehd1 EH-domain containing 1 gene MP:0003671 abnormal eyelid aperture IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20200310 MGI 1619277 Ehd1 EH-domain containing 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:16445686 1619277 Ehd1 EH-domain containing 1 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0009851 abnormal Sertoli cell phagocytosis IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20200310 MGI PMID:17284518 1619277 Ehd1 EH-domain containing 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:20359371 1619277 Ehd1 EH-domain containing 1 gene MP:0031345 developmental cataract IAGP N RGD:5509061 20220217 MGI PMID:20359371 1619281 Efna3 ephrin A3 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:16025107 1619281 Efna3 ephrin A3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12914696 1619281 Efna3 ephrin A3 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20150625 MGI PMID:25281279 1619281 Efna3 ephrin A3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20150827 MGI PMID:25281279 1619281 Efna3 ephrin A3 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:12914696 1619281 Efna3 ephrin A3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20150625 MGI PMID:25281279 1619281 Efna3 ephrin A3 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20150625 MGI PMID:25281279 1619281 Efna3 ephrin A3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20150625 MGI PMID:25281279 1619281 Efna3 ephrin A3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19734893 1619281 Efna3 ephrin A3 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20150625 MGI PMID:25281279 1619281 Efna3 ephrin A3 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20150625 MGI PMID:25281279 1619281 Efna3 ephrin A3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12914696 1619281 Efna3 ephrin A3 gene MP:0002634 abnormal sensorimotor gating IAGP N RGD:5509061 20150625 MGI PMID:25281279 1619281 Efna3 ephrin A3 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:12914696 1619281 Efna3 ephrin A3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20150625 MGI PMID:25281279 1619281 Efna3 ephrin A3 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20150625 MGI PMID:25281279 1619281 Efna3 ephrin A3 gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:19734893 1619281 Efna3 ephrin A3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:19734893 1619281 Efna3 ephrin A3 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:19592509 1619281 Efna3 ephrin A3 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20150625 MGI PMID:25281279 1619281 Efna3 ephrin A3 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19592509 1619281 Efna3 ephrin A3 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19592509 1619281 Efna3 ephrin A3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12914696 1619282 Cbfa2t3 CBFA2/RUNX1 translocation partner 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18710942 1619282 Cbfa2t3 CBFA2/RUNX1 translocation partner 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18710942 1619282 Cbfa2t3 CBFA2/RUNX1 translocation partner 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18710942 1619282 Cbfa2t3 CBFA2/RUNX1 translocation partner 3 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18710942 1619282 Cbfa2t3 CBFA2/RUNX1 translocation partner 3 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18710942 1619282 Cbfa2t3 CBFA2/RUNX1 translocation partner 3 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:18710942 1619282 Cbfa2t3 CBFA2/RUNX1 translocation partner 3 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18710942 1619282 Cbfa2t3 CBFA2/RUNX1 translocation partner 3 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18710942 1619282 Cbfa2t3 CBFA2/RUNX1 translocation partner 3 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18710942 1619282 Cbfa2t3 CBFA2/RUNX1 translocation partner 3 gene MP:0010178 increased number of Howell-Jolly bodies IAGP N RGD:5509061 20141003 MGI PMID:18710942 1619282 Cbfa2t3 CBFA2/RUNX1 translocation partner 3 gene MP:0031276 abnormal stress erythropoiesis IAGP N RGD:5509061 20210805 MGI PMID:18710942 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16227606 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:16227606 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0001147 small testis IAGP N RGD:5509061 20170511 MGI PMID:27281218 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20170511 MGI PMID:27281218 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:16227606 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16227606 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0001924 infertility IAGP N RGD:5509061 20170511 MGI PMID:27281218 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20170511 MGI PMID:27281218 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20170511 MGI PMID:27281218 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20170511 MGI PMID:27281218 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20170511 MGI PMID:27281218 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20170511 MGI PMID:27281218 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:16227606 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16227606 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20170511 MGI PMID:27281218 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20170511 MGI PMID:27281218 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0005158 ovary hypoplasia IAGP N RGD:5509061 20170511 MGI PMID:27281218 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0008391 abnormal primordial germ cell morphology IAGP N RGD:5509061 20170511 MGI PMID:27281218 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20170511 MGI PMID:27281218 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:16227606 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0010802 abnormal intestinal enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16227606 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16227606 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20170511 MGI PMID:27281218 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20150312 MGI PMID:16227606 1619284 Cbfa2t2 CBFA2/RUNX1 translocation partner 2 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:27281218 1619285 Ctnna2 catenin alpha 2 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20200310 MGI PMID:12123610 1619285 Ctnna2 catenin alpha 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20200310 MGI PMID:12123610 1619285 Ctnna2 catenin alpha 2 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:9060409 1619285 Ctnna2 catenin alpha 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20200310 MGI PMID:11413545 1619285 Ctnna2 catenin alpha 2 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20200310 MGI PMID:11413545 1619285 Ctnna2 catenin alpha 2 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20200310 MGI PMID:9060409 1619285 Ctnna2 catenin alpha 2 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20200310 MGI PMID:11413545 1619285 Ctnna2 catenin alpha 2 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20200310 MGI PMID:11835672 1619285 Ctnna2 catenin alpha 2 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20200310 MGI PMID:9060409 1619285 Ctnna2 catenin alpha 2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20200310 MGI PMID:9060409 1619285 Ctnna2 catenin alpha 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:9060409 1619285 Ctnna2 catenin alpha 2 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20200310 MGI PMID:9060409 1619285 Ctnna2 catenin alpha 2 gene MP:0001391 abnormal tail movements IAGP N RGD:5509061 20200310 MGI PMID:9060409 1619285 Ctnna2 catenin alpha 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:9060409 1619285 Ctnna2 catenin alpha 2 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20200310 MGI PMID:12089526 1619285 Ctnna2 catenin alpha 2 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20200310 MGI PMID:12089526 1619285 Ctnna2 catenin alpha 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:9060409 1619285 Ctnna2 catenin alpha 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:9060409 1619285 Ctnna2 catenin alpha 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:12123610 1619285 Ctnna2 catenin alpha 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:9060409 1619285 Ctnna2 catenin alpha 2 gene MP:0004812 abnormal linear vestibular evoked potential IAGP N RGD:5509061 20200310 MGI PMID:16235133 1619285 Ctnna2 catenin alpha 2 gene MP:0004814 reduced linear vestibular evoked potential IAGP N RGD:5509061 20200310 MGI PMID:16235133 1619285 Ctnna2 catenin alpha 2 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20200310 MGI PMID:11413545 1619285 Ctnna2 catenin alpha 2 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20200310 MGI PMID:11835672 1619285 Ctnna2 catenin alpha 2 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20200310 MGI PMID:12089526 1619285 Ctnna2 catenin alpha 2 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20200310 MGI PMID:11413545 1619285 Ctnna2 catenin alpha 2 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20200310 MGI PMID:11835672 1619285 Ctnna2 catenin alpha 2 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20200310 MGI PMID:9060409 1619285 Ctnna2 catenin alpha 2 gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20200310 MGI PMID:11835672 1619285 Ctnna2 catenin alpha 2 gene MP:0010011 ectopic hippocampus pyramidal cells IAGP N RGD:5509061 20200310 MGI PMID:11835672 1619285 Ctnna2 catenin alpha 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12123610 1619288 Casq1 calsequestrin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17627988 1619288 Casq1 calsequestrin 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:17627988 1619288 Casq1 calsequestrin 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:17627988 1619288 Casq1 calsequestrin 1 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17627988 1619288 Casq1 calsequestrin 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17627988 1619288 Casq1 calsequestrin 1 gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:17627988 1619288 Casq1 calsequestrin 1 gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:17627988 1619288 Casq1 calsequestrin 1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:17627988 1619288 Casq1 calsequestrin 1 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17627988 1619288 Casq1 calsequestrin 1 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20201022 MGI 1619288 Casq1 calsequestrin 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20201022 MGI 1619288 Casq1 calsequestrin 1 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 1619288 Casq1 calsequestrin 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1619288 Casq1 calsequestrin 1 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20210128 MGI 1619289 Aspm abnormal spindle microtubule assembly gene MP:0000433 microcephaly IAGP N RGD:5509061 20200310 MGI PMID:20823249 1619289 Aspm abnormal spindle microtubule assembly gene MP:0000433 microcephaly IAGP N RGD:5509061 20200310 MGI PMID:26581405 1619289 Aspm abnormal spindle microtubule assembly gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:20823249 1619289 Aspm abnormal spindle microtubule assembly gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20200310 MGI PMID:26581405 1619289 Aspm abnormal spindle microtubule assembly gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:24220505 1619289 Aspm abnormal spindle microtubule assembly gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20200310 MGI PMID:24220505 1619289 Aspm abnormal spindle microtubule assembly gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:24220505 1619289 Aspm abnormal spindle microtubule assembly gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:20823249 1619289 Aspm abnormal spindle microtubule assembly gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20200310 MGI 1619289 Aspm abnormal spindle microtubule assembly gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:20823249 1619289 Aspm abnormal spindle microtubule assembly gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:20823249 1619289 Aspm abnormal spindle microtubule assembly gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20200310 MGI PMID:20823249 1619289 Aspm abnormal spindle microtubule assembly gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20200310 MGI PMID:24220505 1619289 Aspm abnormal spindle microtubule assembly gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20200310 MGI PMID:26581405 1619289 Aspm abnormal spindle microtubule assembly gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20240718 MGI PMID:34237032 1619289 Aspm abnormal spindle microtubule assembly gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:26581405 1619289 Aspm abnormal spindle microtubule assembly gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:20823249 1619289 Aspm abnormal spindle microtubule assembly gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:20823249 1619289 Aspm abnormal spindle microtubule assembly gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:24220505 1619289 Aspm abnormal spindle microtubule assembly gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20200310 MGI PMID:24220505 1619289 Aspm abnormal spindle microtubule assembly gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:26581405 1619289 Aspm abnormal spindle microtubule assembly gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20200310 MGI 1619289 Aspm abnormal spindle microtubule assembly gene MP:0003443 increased circulating glycerol level IEA N RGD:5509061 20211021 MGI 1619289 Aspm abnormal spindle microtubule assembly gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1619289 Aspm abnormal spindle microtubule assembly gene MP:0003989 abnormal barrel cortex morphology IAGP N RGD:5509061 20200310 MGI PMID:24220505 1619289 Aspm abnormal spindle microtubule assembly gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:20823249 1619289 Aspm abnormal spindle microtubule assembly gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20200310 MGI PMID:20823249 1619289 Aspm abnormal spindle microtubule assembly gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20200310 MGI PMID:26581405 1619289 Aspm abnormal spindle microtubule assembly gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20200310 MGI 1619289 Aspm abnormal spindle microtubule assembly gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20200310 MGI PMID:24220505 1619289 Aspm abnormal spindle microtubule assembly gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20200310 MGI PMID:26581405 1619289 Aspm abnormal spindle microtubule assembly gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20200310 MGI PMID:24220505 1619289 Aspm abnormal spindle microtubule assembly gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20200310 MGI PMID:24220505 1619289 Aspm abnormal spindle microtubule assembly gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20200310 MGI PMID:20823249 1619289 Aspm abnormal spindle microtubule assembly gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20240718 MGI PMID:34237032 1619289 Aspm abnormal spindle microtubule assembly gene MP:0009235 small sperm head IAGP N RGD:5509061 20200310 MGI PMID:20823249 1619289 Aspm abnormal spindle microtubule assembly gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20200402 MGI 1619289 Aspm abnormal spindle microtubule assembly gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20240718 MGI PMID:34237032 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0000849 abnormal cerebellum morphology IEA N RGD:5509061 20120112 MGI 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:21937600 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20150205 MGI PMID:24491816 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:21937600 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:21937600 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20150205 MGI PMID:24491816 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20150205 MGI PMID:24491816 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:21937600 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:21937600 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21937600 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0001393 ataxia IEA N RGD:5509061 20120112 MGI 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21937600 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:21937600 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0005449 abnormal food intake IEA N RGD:5509061 20120112 MGI 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:21937600 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20150205 MGI PMID:24491816 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0008579 abnormal Purkinje cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21937600 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0008579 abnormal Purkinje cell differentiation IAGP N RGD:5509061 20150205 MGI PMID:24491816 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:21937600 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20150205 MGI PMID:24491816 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0009890 cleft secondary palate IEA N RGD:5509061 20120112 MGI 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0010008 abnormal Purkinje cell migration IAGP N RGD:5509061 20150205 MGI PMID:24491816 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20150205 MGI PMID:24491816 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21937600 1619466 Skor2 SKI family transcriptional corepressor 2 gene MP:0013551 decreased cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20161201 MGI PMID:21937600 1619475 Defb43 defensin beta 43 gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20211021 MGI 1619475 Defb43 defensin beta 43 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1619488 Nlrp1b NLR family, pyrin domain containing 1B gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:22753929 1619488 Nlrp1b NLR family, pyrin domain containing 1B gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22753929 1619488 Nlrp1b NLR family, pyrin domain containing 1B gene MP:0005571 decreased lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:22753929 1619488 Nlrp1b NLR family, pyrin domain containing 1B gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:22753929 1619488 Nlrp1b NLR family, pyrin domain containing 1B gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22753929 1619519 Btbd8 BTB domain containing 8 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1619519 Btbd8 BTB domain containing 8 gene MP:0000274 enlarged heart IEA N RGD:5509061 20201022 MGI 1619519 Btbd8 BTB domain containing 8 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20201022 MGI 1619519 Btbd8 BTB domain containing 8 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 1619519 Btbd8 BTB domain containing 8 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 1619519 Btbd8 BTB domain containing 8 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1619519 Btbd8 BTB domain containing 8 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20240704 MGI PMID:38558797 1619519 Btbd8 BTB domain containing 8 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20240704 MGI PMID:38558797 1619519 Btbd8 BTB domain containing 8 gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20240704 MGI PMID:38558797 1619519 Btbd8 BTB domain containing 8 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20240704 MGI PMID:38558797 1619519 Btbd8 BTB domain containing 8 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20211021 MGI 1619519 Btbd8 BTB domain containing 8 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20240704 MGI PMID:38558797 1619519 Btbd8 BTB domain containing 8 gene MP:0014201 abnormal intestinal epithelium physiology IAGP N RGD:5509061 20240704 MGI PMID:38558797 1619519 Btbd8 BTB domain containing 8 gene MP:0014221 increased colon goblet cell number IAGP N RGD:5509061 20240704 MGI PMID:38558797 1619543 Dok6 docking protein 6 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20220811 MGI 1619548 Tmem170b transmembrane protein 170B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1619567 Zfp551 zinc finger protein 551 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20240523 MGI 1619567 Zfp551 zinc finger protein 551 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1619567 Zfp551 zinc finger protein 551 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1619574 Muc3a mucin 3A, cell surface associated gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 1619575 4930567H17Rik RIKEN cDNA 4930567H17 gene gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230420 MGI PMID:35595785 1619597 Ccl26 C-C motif chemokine ligand 26 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1619597 Ccl26 C-C motif chemokine ligand 26 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20160421 MGI 1619597 Ccl26 C-C motif chemokine ligand 26 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1619597 Ccl26 C-C motif chemokine ligand 26 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20211021 MGI 1619608 Taar8c trace amine-associated receptor 8C gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 1619608 Taar8c trace amine-associated receptor 8C gene MP:0000601 small liver IEA N RGD:5509061 20210826 MGI 1619608 Taar8c trace amine-associated receptor 8C gene MP:0001200 thick skin IEA N RGD:5509061 20210826 MGI 1619608 Taar8c trace amine-associated receptor 8C gene MP:0001293 anophthalmia IEA N RGD:5509061 20210826 MGI 1619608 Taar8c trace amine-associated receptor 8C gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1619608 Taar8c trace amine-associated receptor 8C gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1619608 Taar8c trace amine-associated receptor 8C gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1619608 Taar8c trace amine-associated receptor 8C gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1619610 Apcdd1 adenomatosis polyposis coli down-regulated 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1619610 Apcdd1 adenomatosis polyposis coli down-regulated 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1619610 Apcdd1 adenomatosis polyposis coli down-regulated 1 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1619610 Apcdd1 adenomatosis polyposis coli down-regulated 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1619610 Apcdd1 adenomatosis polyposis coli down-regulated 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1619610 Apcdd1 adenomatosis polyposis coli down-regulated 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1619610 Apcdd1 adenomatosis polyposis coli down-regulated 1 gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 1619610 Apcdd1 adenomatosis polyposis coli down-regulated 1 gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20231109 MGI PMID:36325906 1619610 Apcdd1 adenomatosis polyposis coli down-regulated 1 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20231109 MGI PMID:36325906 1619610 Apcdd1 adenomatosis polyposis coli down-regulated 1 gene MP:0004937 dilated heart IAGP N RGD:5509061 20231109 MGI PMID:36325906 1619610 Apcdd1 adenomatosis polyposis coli down-regulated 1 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1619610 Apcdd1 adenomatosis polyposis coli down-regulated 1 gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20191114 MGI PMID:29154126 1619610 Apcdd1 adenomatosis polyposis coli down-regulated 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1619610 Apcdd1 adenomatosis polyposis coli down-regulated 1 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20231109 MGI PMID:36325906 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20141003 MGI 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0000644 dextrocardia IEA N RGD:5509061 20141003 MGI 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0002725 abnormal vein morphology IEA N RGD:5509061 20141003 MGI 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0003178 left pulmonary isomerism IEA N RGD:5509061 20141003 MGI 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20210826 MGI 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0004113 abnormal aortic arch morphology IEA N RGD:5509061 20141003 MGI 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0004158 right aortic arch IEA N RGD:5509061 20141003 MGI 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0004703 abnormal vertebral column morphology IEA N RGD:5509061 20141003 MGI 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20141003 MGI 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0011249 abdominal situs inversus IEA N RGD:5509061 20141003 MGI 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0011250 abdominal situs ambiguus IEA N RGD:5509061 20141003 MGI 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0011252 situs inversus totalis IEA N RGD:5509061 20141003 MGI 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0011649 immotile respiratory cilia IEA N RGD:5509061 20141003 MGI 1619616 Dnaaf3 dynein, axonemal assembly factor 3 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20141003 MGI 1619620 Hbb-bh2 hemoglobin beta, bh2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20200310 MGI 1619620 Hbb-bh2 hemoglobin beta, bh2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20200310 MGI 1619625 Ldoc1 regulator of NFKB signaling gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20181220 MGI PMID:25468940 1619625 Ldoc1 regulator of NFKB signaling gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20181220 MGI PMID:25468940 1619625 Ldoc1 regulator of NFKB signaling gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20181220 MGI PMID:25468940 1619625 Ldoc1 regulator of NFKB signaling gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20181220 MGI PMID:25468940 1619625 Ldoc1 regulator of NFKB signaling gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20181220 MGI PMID:25468940 1619625 Ldoc1 regulator of NFKB signaling gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20181220 MGI PMID:25468940 1619625 Ldoc1 regulator of NFKB signaling gene MP:0011384 abnormal progesterone level IAGP N RGD:5509061 20181220 MGI PMID:25468940 1619625 Ldoc1 regulator of NFKB signaling gene MP:0012008 delayed parturition IAGP N RGD:5509061 20181220 MGI PMID:25468940 1619625 Ldoc1 regulator of NFKB signaling gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20191219 MGI PMID:25468940 1619627 Ccdc160 coiled-coil domain containing 160 gene MP:0000292 distended pericardium IEA N RGD:5509061 20111116 MGI 1619627 Ccdc160 coiled-coil domain containing 160 gene MP:0000928 incomplete rostral neuropore closure IEA N RGD:5509061 20111116 MGI 1619627 Ccdc160 coiled-coil domain containing 160 gene MP:0000929 open neural tube IEA N RGD:5509061 20111116 MGI 1619627 Ccdc160 coiled-coil domain containing 160 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20111116 MGI 1619627 Ccdc160 coiled-coil domain containing 160 gene MP:0003400 kinked neural tube IEA N RGD:5509061 20111116 MGI 1619627 Ccdc160 coiled-coil domain containing 160 gene MP:0004073 caudal body truncation IEA N RGD:5509061 20141003 MGI 1619627 Ccdc160 coiled-coil domain containing 160 gene MP:0009328 delayed heart looping IEA N RGD:5509061 20111116 MGI 1619627 Ccdc160 coiled-coil domain containing 160 gene MP:0009657 failure of chorioallantoic fusion IEA N RGD:5509061 20111116 MGI 1619640 AA467197 expressed sequence AA467197 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20240509 MGI PMID:38296961 1619640 AA467197 expressed sequence AA467197 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20240509 MGI PMID:38296961 1619640 AA467197 expressed sequence AA467197 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20240509 MGI PMID:38296961 1619640 AA467197 expressed sequence AA467197 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20240509 MGI PMID:38296961 1619640 AA467197 expressed sequence AA467197 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20240509 MGI PMID:38296961 1619640 AA467197 expressed sequence AA467197 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20240509 MGI PMID:38296961 1619640 AA467197 expressed sequence AA467197 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20240509 MGI PMID:38296961 1619640 AA467197 expressed sequence AA467197 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20240509 MGI PMID:38296961 1619640 AA467197 expressed sequence AA467197 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20240509 MGI PMID:38296961 1619640 AA467197 expressed sequence AA467197 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20240509 MGI PMID:38296961 1619640 AA467197 expressed sequence AA467197 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20240509 MGI PMID:38296961 1619640 AA467197 expressed sequence AA467197 gene MP:0012604 decreased glutathione level IAGP N RGD:5509061 20240509 MGI PMID:38296961 1619640 AA467197 expressed sequence AA467197 gene MP:0014245 increased cellular ATP level IAGP N RGD:5509061 20240509 MGI PMID:38296961 1619640 AA467197 expressed sequence AA467197 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20240509 MGI PMID:38296961 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:15186781 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:15737743 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:18353676 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20160825 MGI PMID:27466441 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15186781 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0001003 abnormal olfactory receptor morphology IAGP N RGD:5509061 20141003 MGI PMID:24211702 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0001003 abnormal olfactory receptor morphology IAGP N RGD:5509061 20160825 MGI PMID:27466441 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:15186782 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:15186782 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:18353676 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:24211702 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20180308 MGI PMID:27844052 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15186782 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:15186782 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15737743 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17521568 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20160825 MGI PMID:27466441 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20180524 MGI PMID:29407371 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20160825 MGI PMID:27466441 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0009941 abnormal olfactory bulb interneuron morphology IAGP N RGD:5509061 20160825 MGI PMID:27466441 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20160825 MGI PMID:27466441 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15186781 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0020348 decreased olfactory sensory neuron number IAGP N RGD:5509061 20160915 MGI PMID:27466441 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0020348 decreased olfactory sensory neuron number IAGP N RGD:5509061 20161229 MGI PMID:23884929 1619644 Or8a1 olfactory receptor family 8 subfamily A member 1 gene MP:0020348 decreased olfactory sensory neuron number IAGP N RGD:5509061 20180524 MGI PMID:29407371 1619652 Ugt1a6b UDP glucuronosyltransferase 1 family, polypeptide A6B gene MP:0001293 anophthalmia IEA N RGD:5509061 20221215 MGI 1619652 Ugt1a6b UDP glucuronosyltransferase 1 family, polypeptide A6B gene MP:0001297 microphthalmia IEA N RGD:5509061 20221215 MGI 1619657 Eid2 EP300 interacting inhibitor of differentiation 2 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1619657 Eid2 EP300 interacting inhibitor of differentiation 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1619657 Eid2 EP300 interacting inhibitor of differentiation 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1619658 Zfp640 zinc finger protein 640 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1619658 Zfp640 zinc finger protein 640 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1619658 Zfp640 zinc finger protein 640 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:17143286 1619658 Zfp640 zinc finger protein 640 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17143286 1619658 Zfp640 zinc finger protein 640 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1619658 Zfp640 zinc finger protein 640 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17143286 1619658 Zfp640 zinc finger protein 640 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:17143286 1619658 Zfp640 zinc finger protein 640 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:17143286 1619658 Zfp640 zinc finger protein 640 gene MP:0009895 decreased palatine bone horizontal plate size IAGP N RGD:5509061 20141003 MGI PMID:17143286 1619658 Zfp640 zinc finger protein 640 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:17143286 1619658 Zfp640 zinc finger protein 640 gene MP:0030383 small presphenoid bone IAGP N RGD:5509061 20171207 MGI PMID:17143286 1619659 Thoc6 THO complex 6 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1619659 Thoc6 THO complex 6 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20240321 MGI PMID:38388531 1619659 Thoc6 THO complex 6 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20181227 MGI 1619659 Thoc6 THO complex 6 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20221215 MGI 1619659 Thoc6 THO complex 6 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1619659 Thoc6 THO complex 6 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1619659 Thoc6 THO complex 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20240321 MGI PMID:38388531 1619659 Thoc6 THO complex 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240321 MGI PMID:38388531 1619659 Thoc6 THO complex 6 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20221215 MGI 1619659 Thoc6 THO complex 6 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20240321 MGI PMID:38388531 1619659 Thoc6 THO complex 6 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20181227 MGI 1619659 Thoc6 THO complex 6 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20211021 MGI 1619659 Thoc6 THO complex 6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20240321 MGI PMID:38388531 1619659 Thoc6 THO complex 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1619659 Thoc6 THO complex 6 gene MP:0012705 increased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20240321 MGI PMID:38388531 1619659 Thoc6 THO complex 6 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1619659 Thoc6 THO complex 6 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20240321 MGI PMID:38388531 1619660 Rnf133 ring finger protein 133 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20241017 MGI PMID:35831855 1619660 Rnf133 ring finger protein 133 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20241017 MGI PMID:35831855 1619660 Rnf133 ring finger protein 133 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20241017 MGI PMID:35831855 1619660 Rnf133 ring finger protein 133 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20241017 MGI PMID:35831855 1619660 Rnf133 ring finger protein 133 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20241017 MGI PMID:35831855 1619660 Rnf133 ring finger protein 133 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20241017 MGI PMID:35831855 1619660 Rnf133 ring finger protein 133 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20241017 MGI PMID:35831855 1619660 Rnf133 ring finger protein 133 gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20241017 MGI PMID:35831855 1619660 Rnf133 ring finger protein 133 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20220519 MGI 1619660 Rnf133 ring finger protein 133 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20241017 MGI PMID:35831855 1619663 Frmd7 FERM domain containing 7 gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20210128 MGI PMID:33007925 1619669 Slc25a34 solute carrier family 25, member 34 gene MP:0001260 increased body weight IAGP N RGD:5509061 20240418 MGI PMID:35718058 1619669 Slc25a34 solute carrier family 25, member 34 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240418 MGI PMID:35718058 1619669 Slc25a34 solute carrier family 25, member 34 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20240418 MGI PMID:35718058 1619669 Slc25a34 solute carrier family 25, member 34 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20240418 MGI PMID:35718058 1619669 Slc25a34 solute carrier family 25, member 34 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20240418 MGI PMID:35718058 1619669 Slc25a34 solute carrier family 25, member 34 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20240418 MGI PMID:35718058 1619669 Slc25a34 solute carrier family 25, member 34 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20240418 MGI PMID:35718058 1619669 Slc25a34 solute carrier family 25, member 34 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20240418 MGI PMID:35718058 1619669 Slc25a34 solute carrier family 25, member 34 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20240418 MGI PMID:35718058 1619669 Slc25a34 solute carrier family 25, member 34 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20240418 MGI PMID:35718058 1619669 Slc25a34 solute carrier family 25, member 34 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20240418 MGI PMID:35718058 1619670 Cfap57 cilia and flagella associated protein 57 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20210520 MGI 1619670 Cfap57 cilia and flagella associated protein 57 gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20210520 MGI 1619670 Cfap57 cilia and flagella associated protein 57 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20210128 MGI 1619670 Cfap57 cilia and flagella associated protein 57 gene MP:0001925 male infertility IAGP N RGD:5509061 20231005 MGI PMID:36752199 1619670 Cfap57 cilia and flagella associated protein 57 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210128 MGI 1619670 Cfap57 cilia and flagella associated protein 57 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20231005 MGI PMID:36752199 1619670 Cfap57 cilia and flagella associated protein 57 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20231005 MGI PMID:36752199 1619670 Cfap57 cilia and flagella associated protein 57 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20231005 MGI PMID:36752199 1619670 Cfap57 cilia and flagella associated protein 57 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20231005 MGI PMID:36752199 1619670 Cfap57 cilia and flagella associated protein 57 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20231005 MGI PMID:36752199 1619670 Cfap57 cilia and flagella associated protein 57 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20231005 MGI PMID:36752199 1619670 Cfap57 cilia and flagella associated protein 57 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20231005 MGI PMID:36752199 1619683 Gpr176 G protein-coupled receptor 176 gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20200514 MGI 1619683 Gpr176 G protein-coupled receptor 176 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1619683 Gpr176 G protein-coupled receptor 176 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20201015 MGI PMID:26882873 1619686 Cdh26 cadherin-like 26 gene MP:0005575 increased pulmonary ventilation IEA N RGD:5509061 20210128 MGI 1619686 Cdh26 cadherin-like 26 gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20210128 MGI 1619686 Cdh26 cadherin-like 26 gene MP:0005586 decreased tidal volume IEA N RGD:5509061 20210520 MGI 1619686 Cdh26 cadherin-like 26 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20231207 MGI 1619686 Cdh26 cadherin-like 26 gene MP:0012125 decreased bronchoconstrictive response IEA N RGD:5509061 20201022 MGI 1619690 Kdm7a lysine (K)-specific demethylase 7A gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 1619690 Kdm7a lysine (K)-specific demethylase 7A gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 1619690 Kdm7a lysine (K)-specific demethylase 7A gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 1619690 Kdm7a lysine (K)-specific demethylase 7A gene MP:0003036 vertebral transformation IEA N RGD:5509061 20170105 MGI 1619690 Kdm7a lysine (K)-specific demethylase 7A gene MP:0009759 abnormal hair follicle bulge morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 1619691 Frem3 Fras1 related extracellular matrix protein 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 1619691 Frem3 Fras1 related extracellular matrix protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201001 MGI PMID:31554749 1619696 Htra4 HtrA serine peptidase 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:26353049 1619697 Nek5 NIMA (never in mitosis gene a)-related expressed kinase 5 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20160929 MGI PMID:27534441 1619701 Myo3b myosin IIIB gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20181227 MGI 1619701 Myo3b myosin IIIB gene MP:0000947 convulsive seizures IEA N RGD:5509061 20201231 MGI 1619701 Myo3b myosin IIIB gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1619701 Myo3b myosin IIIB gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1619701 Myo3b myosin IIIB gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20240321 MGI PMID:26926603 1619701 Myo3b myosin IIIB gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230601 MGI 1619701 Myo3b myosin IIIB gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240321 MGI PMID:26926603 1619702 Nostrin nitric oxide synthase trafficker gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22751148 1619702 Nostrin nitric oxide synthase trafficker gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20160623 MGI PMID:22751148 1619702 Nostrin nitric oxide synthase trafficker gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:22751148 1619702 Nostrin nitric oxide synthase trafficker gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:22751148 1619702 Nostrin nitric oxide synthase trafficker gene MP:0020316 decreased vascular endothelial cell proliferation IAGP N RGD:5509061 20160623 MGI PMID:22751148 1619703 Abhd12b abhydrolase domain containing 12B gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1619705 Lipi lipase, member I gene MP:0000424 retarded hair growth IAGP N RGD:5509061 20141003 MGI PMID:9499429 1619705 Lipi lipase, member I gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9499429 1619705 Lipi lipase, member I gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9499429 1619705 Lipi lipase, member I gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9499429 1619705 Lipi lipase, member I gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9499429 1619705 Lipi lipase, member I gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9499429 1619705 Lipi lipase, member I gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9499429 1619705 Lipi lipase, member I gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:9499429 1619705 Lipi lipase, member I gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9499429 1619706 Lyset lysosomal enzyme trafficking factor gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20221201 MGI PMID:36074821 1619706 Lyset lysosomal enzyme trafficking factor gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20221201 MGI PMID:36074821 1619706 Lyset lysosomal enzyme trafficking factor gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20221201 MGI PMID:36074821 1619706 Lyset lysosomal enzyme trafficking factor gene MP:0020261 increased beta-galactosidase level IAGP N RGD:5509061 20221201 MGI PMID:36074821 1619707 Lypd6 LY6/PLAUR domain containing 6 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1619707 Lypd6 LY6/PLAUR domain containing 6 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170105 MGI 1619707 Lypd6 LY6/PLAUR domain containing 6 gene MP:0001147 small testis IEA N RGD:5509061 20170105 MGI 1619707 Lypd6 LY6/PLAUR domain containing 6 gene MP:0001192 scaly skin IEA N RGD:5509061 20181227 MGI 1619707 Lypd6 LY6/PLAUR domain containing 6 gene MP:0001200 thick skin IEA N RGD:5509061 20181227 MGI 1619707 Lypd6 LY6/PLAUR domain containing 6 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1619707 Lypd6 LY6/PLAUR domain containing 6 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1619707 Lypd6 LY6/PLAUR domain containing 6 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1619709 H4c16 H4 histone 16 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1619709 H4c16 H4 histone 16 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230601 MGI 1619709 H4c16 H4 histone 16 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1619714 Zar1 zygote arrest 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12539046 1619714 Zar1 zygote arrest 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20210520 MGI PMID:31598710 1619714 Zar1 zygote arrest 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:12539046 1619714 Zar1 zygote arrest 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20210520 MGI PMID:31598710 1619714 Zar1 zygote arrest 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20210520 MGI PMID:31598710 1619714 Zar1 zygote arrest 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20210520 MGI PMID:31598710 1619714 Zar1 zygote arrest 1 gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20210520 MGI PMID:31598710 1619714 Zar1 zygote arrest 1 gene MP:0014443 impaired polar body extrusion IAGP N RGD:5509061 20240509 MGI PMID:31598710 1619717 Sbsn suprabasin gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1619717 Sbsn suprabasin gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20210204 MGI PMID:32884021 1619717 Sbsn suprabasin gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20210204 MGI PMID:32884021 1619717 Sbsn suprabasin gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20210826 MGI 1619717 Sbsn suprabasin gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20210204 MGI PMID:32884021 1619717 Sbsn suprabasin gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20210204 MGI PMID:32884021 1619717 Sbsn suprabasin gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210520 MGI 1619717 Sbsn suprabasin gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20211021 MGI 1619717 Sbsn suprabasin gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20210204 MGI PMID:32884021 1619717 Sbsn suprabasin gene MP:0008725 increased heart atrium size IEA N RGD:5509061 20210520 MGI 1619717 Sbsn suprabasin gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20210204 MGI PMID:32884021 1619717 Sbsn suprabasin gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 1619720 Trp53i11 transformation related protein 53 inducible protein 11 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1619723 Cnpy1 canopy FGF signaling regulator 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20181227 MGI 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0000745 tremors IEA N RGD:5509061 20221201 MGI 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20180607 MGI PMID:29339520 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20191010 MGI PMID:30137205 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0003063 increased coping response IAGP N RGD:5509061 20191010 MGI PMID:30137205 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20191010 MGI PMID:30137205 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20191010 MGI PMID:30137205 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0003927 increased cellular glucose import IAGP N RGD:5509061 20191010 MGI PMID:30137205 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20191010 MGI PMID:30137205 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20191010 MGI PMID:30137205 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20191010 MGI PMID:30137205 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20191010 MGI PMID:30137205 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20221201 MGI 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20191010 MGI PMID:30137205 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:30137205 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:30137205 1619726 Tafa2 TAFA chemokine like family member 2 gene MP:0020421 increased freezing behavior IAGP N RGD:5509061 20180607 MGI PMID:29339520 1619800 Klhl31 kelch-like 31 gene MP:0000751 myopathy IAGP N RGD:5509061 20181025 MGI PMID:28872460 1619800 Klhl31 kelch-like 31 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20181025 MGI PMID:28872460 1619800 Klhl31 kelch-like 31 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20181025 MGI PMID:28872460 1619800 Klhl31 kelch-like 31 gene MP:0004089 dilated sarcoplasmic reticulum IAGP N RGD:5509061 20181025 MGI PMID:28872460 1619800 Klhl31 kelch-like 31 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20181025 MGI PMID:28872460 1619800 Klhl31 kelch-like 31 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20181025 MGI PMID:28872460 1619800 Klhl31 kelch-like 31 gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20181025 MGI PMID:28872460 1619800 Klhl31 kelch-like 31 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20181025 MGI PMID:28872460 1619800 Klhl31 kelch-like 31 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20181025 MGI PMID:28872460 1619800 Klhl31 kelch-like 31 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20181025 MGI PMID:28872460 1619800 Klhl31 kelch-like 31 gene MP:0010225 abnormal quadriceps morphology IAGP N RGD:5509061 20181025 MGI PMID:28872460 1619800 Klhl31 kelch-like 31 gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20181025 MGI PMID:28872460 1619802 C2cd4a C2 calcium-dependent domain containing 4A gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20181227 MGI 1619803 Ube2q2l ubiquitin conjugating enzyme E2 Q2 like gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20230601 MGI 1619806 Ano2 anoctamin 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1619806 Ano2 anoctamin 2 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1619806 Ano2 anoctamin 2 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1619806 Ano2 anoctamin 2 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 1619806 Ano2 anoctamin 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1619806 Ano2 anoctamin 2 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:21516098 1619806 Ano2 anoctamin 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1619806 Ano2 anoctamin 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1619811 Dytn dystrotelin gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20221215 MGI 1619811 Dytn dystrotelin gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1619811 Dytn dystrotelin gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20220519 MGI 1619811 Dytn dystrotelin gene MP:0002834 decreased heart weight IEA N RGD:5509061 20220519 MGI 1619811 Dytn dystrotelin gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220519 MGI 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:4019727 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220303 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20150528 MGI PMID:4019727 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:19593386 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20191010 MGI PMID:23213481 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20191010 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:4019727 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:4019727 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20191010 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:19593386 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:19593386 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:4019727 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20191010 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:19593386 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20191010 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20150528 MGI PMID:4019727 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20191010 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0002252 abnormal oropharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20191010 MGI PMID:23213481 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20191010 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:4019727 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20191010 MGI PMID:23213481 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0004539 absent maxilla IAGP N RGD:5509061 20191010 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0004541 absent auditory tube IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20191010 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20191010 MGI PMID:23213481 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:4019727 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0006290 proboscis IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0008533 abnormal anterior visceral endoderm morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19593386 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0008926 abnormal anterior definitive endoderm morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20191010 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0009578 otocephaly IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0009578 otocephaly IAGP N RGD:5509061 20141003 MGI PMID:4019727 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0009578 otocephaly IAGP N RGD:5509061 20191010 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0009609 absent basioccipital bone IAGP N RGD:5509061 20191010 MGI PMID:23213481 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:4019727 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0010126 abnormal distal visceral endoderm morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0010335 fused first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20191010 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19593386 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20191010 MGI PMID:23213481 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0011759 absent Rathke's pouch IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0012084 truncated foregut IAGP N RGD:5509061 20141003 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0012176 abnormal head development IAGP N RGD:5509061 20191010 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0013817 absent nasal cavity IAGP N RGD:5509061 20191010 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0030043 small forehead IAGP N RGD:5509061 20170921 MGI PMID:10529425 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0030067 narrow face IAGP N RGD:5509061 20170921 MGI PMID:4019727 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0030071 abnormal face shape IAGP N RGD:5509061 20220303 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0030382 absent paranasal sinus IAGP N RGD:5509061 20191010 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0030464 abnormal cranial cartilage morphology IAGP N RGD:5509061 20191010 MGI PMID:23213481 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20220303 MGI PMID:17711852 1619812 Pgap1 post-GPI attachment to proteins 1 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220303 MGI PMID:17711852 1619816 Mb21d2 Mab-21 domain containing 2 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210128 MGI 1619816 Mb21d2 Mab-21 domain containing 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1619817 Ostn osteocrin gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20170928 MGI PMID:26668395 1619817 Ostn osteocrin gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20170928 MGI PMID:26668395 1619817 Ostn osteocrin gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20170928 MGI PMID:26668395 1619817 Ostn osteocrin gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20170928 MGI PMID:26668395 1619818 Gmnc geminin coiled-coil domain containing gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0001127 small ovary IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170119 MGI PMID:26882546 1619818 Gmnc geminin coiled-coil domain containing gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0001925 male infertility IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0001926 female infertility IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0002262 abnormal nasal mucosa goblet cell morphology IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20170119 MGI PMID:26882546 1619818 Gmnc geminin coiled-coil domain containing gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0005159 azoospermia IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20201022 MGI 1619818 Gmnc geminin coiled-coil domain containing gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20170119 MGI PMID:26882546 1619818 Gmnc geminin coiled-coil domain containing gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0009070 small oviduct IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20220407 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1619818 Gmnc geminin coiled-coil domain containing gene MP:0010861 increased respiratory mucosa goblet cell number IAGP N RGD:5509061 20170119 MGI PMID:26882546 1619818 Gmnc geminin coiled-coil domain containing gene MP:0010861 increased respiratory mucosa goblet cell number IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0010942 abnormal respiratory epithelium morphology IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0011054 absent respiratory motile cilia IAGP N RGD:5509061 20170119 MGI PMID:26882546 1619818 Gmnc geminin coiled-coil domain containing gene MP:0011054 absent respiratory motile cilia IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0011057 absent brain ependyma motile cilia IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170119 MGI PMID:26882546 1619818 Gmnc geminin coiled-coil domain containing gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0011645 absent oviduct epithelium motile cilium IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0012556 increased cell death IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0013206 abnormal motile cilium morphology IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0013236 ovary degeneration IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0030003 hippocampus atrophy IAGP N RGD:5509061 20201015 MGI PMID:26933123 1619818 Gmnc geminin coiled-coil domain containing gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:26933123 1619819 Rtp1 receptor transporter protein 1 gene MP:0001924 infertility IEA N RGD:5509061 20111116 MGI 1619819 Rtp1 receptor transporter protein 1 gene MP:0002739 abnormal olfactory bulb development IEA N RGD:5509061 20111116 MGI 1619821 Rimbp3 RIMS binding protein 3 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:19091768 1619821 Rimbp3 RIMS binding protein 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19091768 1619821 Rimbp3 RIMS binding protein 3 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19091768 1619821 Rimbp3 RIMS binding protein 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19091768 1619821 Rimbp3 RIMS binding protein 3 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:19091768 1619821 Rimbp3 RIMS binding protein 3 gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:19091768 1619821 Rimbp3 RIMS binding protein 3 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:19091768 1619821 Rimbp3 RIMS binding protein 3 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20141003 MGI PMID:19091768 1619821 Rimbp3 RIMS binding protein 3 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19091768 1619821 Rimbp3 RIMS binding protein 3 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:19091768 1619821 Rimbp3 RIMS binding protein 3 gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20141003 MGI PMID:19091768 1619822 Tubal3 tubulin, alpha-like 3 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1619822 Tubal3 tubulin, alpha-like 3 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1619822 Tubal3 tubulin, alpha-like 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1619822 Tubal3 tubulin, alpha-like 3 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210826 MGI 1619822 Tubal3 tubulin, alpha-like 3 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38786026 1619828 Slc38a7 solute carrier family 38, member 7 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1619828 Slc38a7 solute carrier family 38, member 7 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1619828 Slc38a7 solute carrier family 38, member 7 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1619828 Slc38a7 solute carrier family 38, member 7 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1619828 Slc38a7 solute carrier family 38, member 7 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1619828 Slc38a7 solute carrier family 38, member 7 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1619828 Slc38a7 solute carrier family 38, member 7 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1619828 Slc38a7 solute carrier family 38, member 7 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1619828 Slc38a7 solute carrier family 38, member 7 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1619828 Slc38a7 solute carrier family 38, member 7 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1619828 Slc38a7 solute carrier family 38, member 7 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1619828 Slc38a7 solute carrier family 38, member 7 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20230601 MGI 1619830 Ces1f carboxylesterase 1F gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1619830 Ces1f carboxylesterase 1F gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1619830 Ces1f carboxylesterase 1F gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20181227 MGI 1619831 Luzp2 leucine zipper protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12856284 1619832 Nav2 neuron navigator 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1619832 Nav2 neuron navigator 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15158073 1619832 Nav2 neuron navigator 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15158073 1619832 Nav2 neuron navigator 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1619832 Nav2 neuron navigator 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:15158073 1619832 Nav2 neuron navigator 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15158073 1619832 Nav2 neuron navigator 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:15158073 1619832 Nav2 neuron navigator 2 gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:15158073 1619832 Nav2 neuron navigator 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1619832 Nav2 neuron navigator 2 gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 1619832 Nav2 neuron navigator 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20181227 MGI 1619836 Creb5 cAMP responsive element binding protein 5 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19948881 1619836 Creb5 cAMP responsive element binding protein 5 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19948881 1619836 Creb5 cAMP responsive element binding protein 5 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19948881 1619836 Creb5 cAMP responsive element binding protein 5 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19948881 1619836 Creb5 cAMP responsive element binding protein 5 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19948881 1619836 Creb5 cAMP responsive element binding protein 5 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19948881 1619836 Creb5 cAMP responsive element binding protein 5 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19948881 1619836 Creb5 cAMP responsive element binding protein 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19948881 1619837 Fam221a family with sequence similarity 221, member A gene MP:0000160 kyphosis IEA N RGD:5509061 20210826 MGI 1619837 Fam221a family with sequence similarity 221, member A gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1619837 Fam221a family with sequence similarity 221, member A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1619837 Fam221a family with sequence similarity 221, member A gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1619837 Fam221a family with sequence similarity 221, member A gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1619837 Fam221a family with sequence similarity 221, member A gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1619837 Fam221a family with sequence similarity 221, member A gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1619837 Fam221a family with sequence similarity 221, member A gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1619837 Fam221a family with sequence similarity 221, member A gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1619837 Fam221a family with sequence similarity 221, member A gene MP:0002608 increased hematocrit IEA N RGD:5509061 20211021 MGI 1619837 Fam221a family with sequence similarity 221, member A gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1619837 Fam221a family with sequence similarity 221, member A gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20210826 MGI 1619837 Fam221a family with sequence similarity 221, member A gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20210826 MGI 1619837 Fam221a family with sequence similarity 221, member A gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210826 MGI 1619837 Fam221a family with sequence similarity 221, member A gene MP:0010935 increased airway resistance IEA N RGD:5509061 20211021 MGI 1619837 Fam221a family with sequence similarity 221, member A gene MP:0013436 increased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20210826 MGI 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:22654668 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22654668 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230119 MGI 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22654668 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:22654668 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22654668 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22654668 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230119 MGI 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230119 MGI 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0003717 pallor IEA N RGD:5509061 20230119 MGI 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22654668 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:22654668 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230119 MGI 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230119 MGI 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22654668 1619838 Katnal1 katanin p60 subunit A-like 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20230119 MGI 1619847 Otol1 otolin 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1619847 Otol1 otolin 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1619847 Otol1 otolin 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1619847 Otol1 otolin 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1619848 Gpr149 G protein-coupled receptor 149 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:19887567 1619848 Gpr149 G protein-coupled receptor 149 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:19887567 1619848 Gpr149 G protein-coupled receptor 149 gene MP:0001934 increased litter size IAGP N RGD:5509061 20141003 MGI PMID:19887567 1619848 Gpr149 G protein-coupled receptor 149 gene MP:0001968 abnormal touch/ nociception IEA N RGD:5509061 20141003 MGI 1619848 Gpr149 G protein-coupled receptor 149 gene MP:0005410 abnormal fertilization IAGP N RGD:5509061 20141003 MGI PMID:19887567 1619848 Gpr149 G protein-coupled receptor 149 gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20141003 MGI PMID:19887567 1619848 Gpr149 G protein-coupled receptor 149 gene MP:0011128 increased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:19887567 1619848 Gpr149 G protein-coupled receptor 149 gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:19887567 1619848 Gpr149 G protein-coupled receptor 149 gene MP:0031411 increased ovulation rate IAGP N RGD:5509061 20220714 MGI PMID:19887567 1619848 Gpr149 G protein-coupled receptor 149 gene MP:0031421 increased superovulation rate IAGP N RGD:5509061 20220714 MGI PMID:19887567 1619848 Gpr149 G protein-coupled receptor 149 gene MP:0031424 enhanced female fertility IAGP N RGD:5509061 20220714 MGI PMID:19887567 1619851 Eif2a eukaryotic translation initiation factor 2A gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1619851 Eif2a eukaryotic translation initiation factor 2A gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1619851 Eif2a eukaryotic translation initiation factor 2A gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 1619851 Eif2a eukaryotic translation initiation factor 2A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1619851 Eif2a eukaryotic translation initiation factor 2A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180111 MGI PMID:27686860 1619851 Eif2a eukaryotic translation initiation factor 2A gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20201022 MGI 1619851 Eif2a eukaryotic translation initiation factor 2A gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1619852 Cerkl ceramide kinase-like gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0001304 cataract IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1619852 Cerkl ceramide kinase-like gene MP:0002090 abnormal vision IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22549043 1619852 Cerkl ceramide kinase-like gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0009392 retina gliosis IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0011963 abnormal total retina thickness IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0020812 long photoreceptor outer segment IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20210923 MGI PMID:32658961 1619852 Cerkl ceramide kinase-like gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:22549043 1619852 Cerkl ceramide kinase-like gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:32658961 1619853 Mettl8 methyltransferase 8, methylcytidine gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20170713 MGI PMID:28655767 1619854 Ppig peptidyl-prolyl isomerase G (cyclophilin G) gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1619855 Becn2 beclin 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23954414 1619855 Becn2 beclin 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23954414 1619855 Becn2 beclin 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23954414 1619855 Becn2 beclin 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23954414 1619855 Becn2 beclin 2 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:23954414 1619855 Becn2 beclin 2 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23954414 1619855 Becn2 beclin 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23954414 1619855 Becn2 beclin 2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:23954414 1619855 Becn2 beclin 2 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:23954414 1619856 Fam170a family with sequence similarity 170, member A gene MP:0001260 increased body weight IAGP N RGD:5509061 20200924 MGI PMID:32588889 1619856 Fam170a family with sequence similarity 170, member A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200924 MGI PMID:32588889 1619856 Fam170a family with sequence similarity 170, member A gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1619856 Fam170a family with sequence similarity 170, member A gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20200924 MGI PMID:32588889 1619856 Fam170a family with sequence similarity 170, member A gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200924 MGI PMID:32588889 1619856 Fam170a family with sequence similarity 170, member A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200924 MGI PMID:32588889 1619856 Fam170a family with sequence similarity 170, member A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200924 MGI PMID:32588889 1619856 Fam170a family with sequence similarity 170, member A gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20200924 MGI PMID:32588889 1619856 Fam170a family with sequence similarity 170, member A gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20200924 MGI PMID:32588889 1619856 Fam170a family with sequence similarity 170, member A gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20200924 MGI PMID:32588889 1619856 Fam170a family with sequence similarity 170, member A gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20200924 MGI PMID:32588889 1619856 Fam170a family with sequence similarity 170, member A gene MP:0009234 absent sperm head IAGP N RGD:5509061 20200924 MGI PMID:32588889 1619856 Fam170a family with sequence similarity 170, member A gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20200924 MGI PMID:32588889 1619856 Fam170a family with sequence similarity 170, member A gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20200924 MGI PMID:32588889 1619856 Fam170a family with sequence similarity 170, member A gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20200924 MGI PMID:32588889 1619858 Gm94 predicted gene 94 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1619858 Gm94 predicted gene 94 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1619858 Gm94 predicted gene 94 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1619858 Gm94 predicted gene 94 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1619861 Tmem260 transmembrane protein 260 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1619861 Tmem260 transmembrane protein 260 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1619861 Tmem260 transmembrane protein 260 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1619863 Susd6 sushi domain containing 6 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1619863 Susd6 sushi domain containing 6 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20210128 MGI 1619863 Susd6 sushi domain containing 6 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20210128 MGI 1619863 Susd6 sushi domain containing 6 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1619863 Susd6 sushi domain containing 6 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1619863 Susd6 sushi domain containing 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141225 MGI PMID:24652652 1619863 Susd6 sushi domain containing 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141225 MGI PMID:24652652 1619863 Susd6 sushi domain containing 6 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1619863 Susd6 sushi domain containing 6 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210128 MGI 1619863 Susd6 sushi domain containing 6 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1619863 Susd6 sushi domain containing 6 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1619863 Susd6 sushi domain containing 6 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1619863 Susd6 sushi domain containing 6 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20221215 MGI 1619863 Susd6 sushi domain containing 6 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1619863 Susd6 sushi domain containing 6 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1619863 Susd6 sushi domain containing 6 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1619863 Susd6 sushi domain containing 6 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210826 MGI 1619866 Ttc6 tetratricopeptide repeat domain 6 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20231102 MGI PMID:37626901 1619866 Ttc6 tetratricopeptide repeat domain 6 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20231102 MGI PMID:37626901 1619866 Ttc6 tetratricopeptide repeat domain 6 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20231102 MGI PMID:37626901 1619866 Ttc6 tetratricopeptide repeat domain 6 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20231102 MGI PMID:37626901 1619866 Ttc6 tetratricopeptide repeat domain 6 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20231102 MGI PMID:37626901 1619870 D930020B18Rik RIKEN cDNA D930020B18 gene gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1619871 Maneal mannosidase, endo-alpha-like gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 1619874 Vezt vezatin, adherens junctions transmembrane protein gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20160421 MGI 1619874 Vezt vezatin, adherens junctions transmembrane protein gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201231 MGI 1619874 Vezt vezatin, adherens junctions transmembrane protein gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:17452094 1619874 Vezt vezatin, adherens junctions transmembrane protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17452094 1619874 Vezt vezatin, adherens junctions transmembrane protein gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1619874 Vezt vezatin, adherens junctions transmembrane protein gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20160421 MGI 1619874 Vezt vezatin, adherens junctions transmembrane protein gene MP:0002959 increased urine microalbumin level IEA N RGD:5509061 20211021 MGI 1619874 Vezt vezatin, adherens junctions transmembrane protein gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:17452094 1619874 Vezt vezatin, adherens junctions transmembrane protein gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:17452094 1619874 Vezt vezatin, adherens junctions transmembrane protein gene MP:0003695 delayed blastocyst hatching from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:17452094 1619874 Vezt vezatin, adherens junctions transmembrane protein gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1619874 Vezt vezatin, adherens junctions transmembrane protein gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17452094 1619874 Vezt vezatin, adherens junctions transmembrane protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619874 Vezt vezatin, adherens junctions transmembrane protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:24019467 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:24019467 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:24019467 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:24019467 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:24019467 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:24019467 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:24019467 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0004648 decreased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:24019467 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0004650 increased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:24019467 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0004651 increased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:24019467 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0008922 abnormal cervical rib IAGP N RGD:5509061 20141003 MGI PMID:24019467 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:24019467 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:24019467 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:24019467 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:24019467 1619875 Wfikkn1 WAP, FS, Ig, KU, and NTR-containing protein 1 gene MP:0021206 abnormal limb muscle morphology IAGP N RGD:5509061 20221201 MGI PMID:24019467 1619876 Chrm5 cholinergic receptor, muscarinic 5 gene MP:0000505 decreased digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:15691866 1619876 Chrm5 cholinergic receptor, muscarinic 5 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:11900778 1619876 Chrm5 cholinergic receptor, muscarinic 5 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:11707605 1619876 Chrm5 cholinergic receptor, muscarinic 5 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:11707605 1619876 Chrm5 cholinergic receptor, muscarinic 5 gene MP:0002503 abnormal histamine physiology IAGP N RGD:5509061 20141003 MGI PMID:15691866 1619876 Chrm5 cholinergic receptor, muscarinic 5 gene MP:0005111 hyperdipsia IAGP N RGD:5509061 20141003 MGI PMID:11900778 1619876 Chrm5 cholinergic receptor, muscarinic 5 gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:18382674 1619876 Chrm5 cholinergic receptor, muscarinic 5 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20141003 MGI PMID:20664521 1619876 Chrm5 cholinergic receptor, muscarinic 5 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:18382674 1619877 Nutm1 NUT midline carcinoma, family member 1 gene MP:0001147 small testis IAGP N RGD:5509061 20210506 MGI PMID:30257209 1619877 Nutm1 NUT midline carcinoma, family member 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20210506 MGI PMID:30257209 1619877 Nutm1 NUT midline carcinoma, family member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20210506 MGI PMID:30257209 1619877 Nutm1 NUT midline carcinoma, family member 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1619877 Nutm1 NUT midline carcinoma, family member 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20210506 MGI PMID:30257209 1619877 Nutm1 NUT midline carcinoma, family member 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20181227 MGI 1619877 Nutm1 NUT midline carcinoma, family member 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20181227 MGI 1619877 Nutm1 NUT midline carcinoma, family member 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1619877 Nutm1 NUT midline carcinoma, family member 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1619878 Xist inactive X specific transcripts gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21389056 1619878 Xist inactive X specific transcripts gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18057104 1619878 Xist inactive X specific transcripts gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:19036803 1619878 Xist inactive X specific transcripts gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11262229 1619878 Xist inactive X specific transcripts gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19036803 1619878 Xist inactive X specific transcripts gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21389056 1619878 Xist inactive X specific transcripts gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10431231 1619878 Xist inactive X specific transcripts gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12900551 1619878 Xist inactive X specific transcripts gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21389056 1619878 Xist inactive X specific transcripts gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:21389056 1619878 Xist inactive X specific transcripts gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:11230177 1619878 Xist inactive X specific transcripts gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:19036803 1619878 Xist inactive X specific transcripts gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21389056 1619878 Xist inactive X specific transcripts gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21852535 1619878 Xist inactive X specific transcripts gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:21389056 1619878 Xist inactive X specific transcripts gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16980619 1619878 Xist inactive X specific transcripts gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:18057104 1619878 Xist inactive X specific transcripts gene MP:0010382 abnormal dosage compensation, by inactivation of X chromosome IAGP N RGD:5509061 20141003 MGI PMID:12952890 1619878 Xist inactive X specific transcripts gene MP:0010382 abnormal dosage compensation, by inactivation of X chromosome IAGP N RGD:5509061 20141003 MGI PMID:15668296 1619878 Xist inactive X specific transcripts gene MP:0010382 abnormal dosage compensation, by inactivation of X chromosome IAGP N RGD:5509061 20141003 MGI PMID:21389056 1619878 Xist inactive X specific transcripts gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:19036803 1619878 Xist inactive X specific transcripts gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18057104 1619878 Xist inactive X specific transcripts gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15992549 1619878 Xist inactive X specific transcripts gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21389056 1619878 Xist inactive X specific transcripts gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19036803 1619878 Xist inactive X specific transcripts gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18057104 1619880 AA986860 expressed sequence AA986860 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1619880 AA986860 expressed sequence AA986860 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1619880 AA986860 expressed sequence AA986860 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1619880 AA986860 expressed sequence AA986860 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1619880 AA986860 expressed sequence AA986860 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220519 MGI 1619882 Lrtm2 leucine-rich repeats and transmembrane domains 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20221117 MGI PMID:35615067 1619882 Lrtm2 leucine-rich repeats and transmembrane domains 2 gene MP:0003063 increased coping response IAGP N RGD:5509061 20221117 MGI PMID:35615067 1619882 Lrtm2 leucine-rich repeats and transmembrane domains 2 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20221117 MGI PMID:35615067 1619882 Lrtm2 leucine-rich repeats and transmembrane domains 2 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20221117 MGI PMID:35615067 1619882 Lrtm2 leucine-rich repeats and transmembrane domains 2 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20221117 MGI PMID:35615067 1619882 Lrtm2 leucine-rich repeats and transmembrane domains 2 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20221117 MGI PMID:35615067 1619882 Lrtm2 leucine-rich repeats and transmembrane domains 2 gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20221117 MGI PMID:35615067 1619882 Lrtm2 leucine-rich repeats and transmembrane domains 2 gene MP:0020875 decreased nervous system dopamine level IAGP N RGD:5509061 20221117 MGI PMID:35615067 1619882 Lrtm2 leucine-rich repeats and transmembrane domains 2 gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20221117 MGI PMID:35615067 1619883 Marchf11 membrane associated ring-CH-type finger 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1619885 Ndufaf8 NADH:ubiquinone oxidoreductase complex assembly factor 8 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20221215 MGI 1619885 Ndufaf8 NADH:ubiquinone oxidoreductase complex assembly factor 8 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1619885 Ndufaf8 NADH:ubiquinone oxidoreductase complex assembly factor 8 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20221215 MGI 1619885 Ndufaf8 NADH:ubiquinone oxidoreductase complex assembly factor 8 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20221215 MGI 1619885 Ndufaf8 NADH:ubiquinone oxidoreductase complex assembly factor 8 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20221215 MGI 1619885 Ndufaf8 NADH:ubiquinone oxidoreductase complex assembly factor 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1619885 Ndufaf8 NADH:ubiquinone oxidoreductase complex assembly factor 8 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1619886 Zbtb7c zinc finger and BTB domain containing 7C gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22253232 1619887 Ccdc154 coiled-coil domain containing 154 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20190103 MGI PMID:20121924 1619887 Ccdc154 coiled-coil domain containing 154 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20190103 MGI PMID:20121924 1619887 Ccdc154 coiled-coil domain containing 154 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20190103 MGI PMID:20121924 1619887 Ccdc154 coiled-coil domain containing 154 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20190103 MGI PMID:20121924 1619887 Ccdc154 coiled-coil domain containing 154 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20190103 MGI PMID:20121924 1619887 Ccdc154 coiled-coil domain containing 154 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20190103 MGI PMID:20121924 1619887 Ccdc154 coiled-coil domain containing 154 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20190103 MGI PMID:20121924 1619887 Ccdc154 coiled-coil domain containing 154 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190103 MGI PMID:20121924 1619887 Ccdc154 coiled-coil domain containing 154 gene MP:0002083 premature death IAGP N RGD:5509061 20190103 MGI PMID:20121924 1619887 Ccdc154 coiled-coil domain containing 154 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20190103 MGI PMID:20121924 1619887 Ccdc154 coiled-coil domain containing 154 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20190103 MGI PMID:20121924 1619887 Ccdc154 coiled-coil domain containing 154 gene MP:0011165 abnormal tooth root development IAGP N RGD:5509061 20190103 MGI PMID:20121924 1619887 Ccdc154 coiled-coil domain containing 154 gene MP:0011166 absent molar root IAGP N RGD:5509061 20190103 MGI PMID:20121924 1619887 Ccdc154 coiled-coil domain containing 154 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20190103 MGI PMID:20121924 1619889 Zfp691 zinc finger protein 691 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20231207 MGI 1619894 Slfnl1 schlafen like 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210708 MGI PMID:32561905 1619895 Cyb5d2 cytochrome b5 domain containing 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1619895 Cyb5d2 cytochrome b5 domain containing 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1619895 Cyb5d2 cytochrome b5 domain containing 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1619895 Cyb5d2 cytochrome b5 domain containing 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1619895 Cyb5d2 cytochrome b5 domain containing 2 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1619895 Cyb5d2 cytochrome b5 domain containing 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 1619897 Nacad NAC alpha domain containing gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1619897 Nacad NAC alpha domain containing gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1619897 Nacad NAC alpha domain containing gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20150108 MGI 1619897 Nacad NAC alpha domain containing gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20150108 MGI 1619898 Oosp1 oocyte secreted protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200723 MGI PMID:32231122 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12066189 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0001588 abnormal hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:12066189 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0001588 abnormal hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:12066189 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0005563 abnormal hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0008850 increased hemoglobin concentration distribution width IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0010175 leptocytosis IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0010177 acanthocytosis IAGP N RGD:5509061 20141003 MGI PMID:12066189 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0010177 acanthocytosis IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0011171 increased number of Heinz bodies IAGP N RGD:5509061 20141003 MGI PMID:12066189 1619900 Ahsp alpha hemoglobin stabilizing protein gene MP:0011171 increased number of Heinz bodies IAGP N RGD:5509061 20141003 MGI PMID:15545996 1619901 Helb helicase (DNA) B gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20170615 MGI PMID:26774285 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210128 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210520 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210520 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20220811 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210128 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210520 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20210128 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20210520 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0009455 enhanced cued conditioning behavior IEA N RGD:5509061 20240523 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0010574 dilated aorta IEA N RGD:5509061 20210520 MGI 1619902 Asb7 ankyrin repeat and SOCS box-containing 7 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0001722 pale yolk sac IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20210708 MGI PMID:33147459 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0002861 abnormal tail bud morphology IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20210708 MGI PMID:33147459 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0009806 abnormal otic vesicle morphology IEA N RGD:5509061 20231207 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1619903 Uqcc3 ubiquinol-cytochrome c reductase complex assembly factor 3 gene MP:0031252 abnormal physiological response to hypoxia IAGP N RGD:5509061 20210708 MGI PMID:33147459 1619907 Krt72 keratin 72 gene MP:0000160 kyphosis IEA N RGD:5509061 20210826 MGI 1619907 Krt72 keratin 72 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210826 MGI 1619907 Krt72 keratin 72 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 1619907 Krt72 keratin 72 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1619907 Krt72 keratin 72 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 1619907 Krt72 keratin 72 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 1619907 Krt72 keratin 72 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1619907 Krt72 keratin 72 gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1619907 Krt72 keratin 72 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1619907 Krt72 keratin 72 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1619907 Krt72 keratin 72 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20210826 MGI 1619907 Krt72 keratin 72 gene MP:0009709 hydrometra IEA N RGD:5509061 20210826 MGI 1619908 Nckap1l NCK associated protein 1 like gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0000314 schistocytosis IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0000604 amyloidosis IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0001262 decreased body weight IEA N RGD:5509061 20200310 MGI 1619908 Nckap1l NCK associated protein 1 like gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0001853 heart inflammation IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0002367 abnormal thymus lobule morphology IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0004733 abnormal thoracic cavity morphology IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0004972 abnormal regulatory T cell number IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0005017 decreased B cell number IEA N RGD:5509061 20200310 MGI 1619908 Nckap1l NCK associated protein 1 like gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20200310 MGI 1619908 Nckap1l NCK associated protein 1 like gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1619908 Nckap1l NCK associated protein 1 like gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0008354 decreased mature gamma-delta T cell number IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0010176 dacryocytosis IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0010177 acanthocytosis IAGP N RGD:5509061 20200310 MGI PMID:19015308 1619908 Nckap1l NCK associated protein 1 like gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1619908 Nckap1l NCK associated protein 1 like gene MP:0010848 decreased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1619908 Nckap1l NCK associated protein 1 like gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1619908 Nckap1l NCK associated protein 1 like gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1619908 Nckap1l NCK associated protein 1 like gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1619908 Nckap1l NCK associated protein 1 like gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1619908 Nckap1l NCK associated protein 1 like gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:19015308 1619910 Mtbp Mdm2, transformed 3T3 cell double minute p53 binding protein gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17906694 1619910 Mtbp Mdm2, transformed 3T3 cell double minute p53 binding protein gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17906694 1619910 Mtbp Mdm2, transformed 3T3 cell double minute p53 binding protein gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:17906694 1619910 Mtbp Mdm2, transformed 3T3 cell double minute p53 binding protein gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17906694 1619910 Mtbp Mdm2, transformed 3T3 cell double minute p53 binding protein gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17906694 1619910 Mtbp Mdm2, transformed 3T3 cell double minute p53 binding protein gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:17906694 1619912 Zc3h10 zinc finger CCCH type containing 10 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200521 MGI PMID:31775033 1619912 Zc3h10 zinc finger CCCH type containing 10 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20200521 MGI PMID:31775033 1619912 Zc3h10 zinc finger CCCH type containing 10 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200521 MGI PMID:31775033 1619912 Zc3h10 zinc finger CCCH type containing 10 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200521 MGI PMID:31775033 1619912 Zc3h10 zinc finger CCCH type containing 10 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20200521 MGI PMID:31775033 1619912 Zc3h10 zinc finger CCCH type containing 10 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20200521 MGI PMID:31775033 1619912 Zc3h10 zinc finger CCCH type containing 10 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20200521 MGI PMID:31775033 1619913 Tmem263 transmembrane protein 263 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0003109 short femur IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619913 Tmem263 transmembrane protein 263 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20240328 MGI PMID:38241182 1619916 Sall4 spalt like transcription factor 4 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19350679 1619916 Sall4 spalt like transcription factor 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19476507 1619916 Sall4 spalt like transcription factor 4 gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:19476507 1619916 Sall4 spalt like transcription factor 4 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19476507 1619916 Sall4 spalt like transcription factor 4 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:18818376 1619916 Sall4 spalt like transcription factor 4 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18818376 1619916 Sall4 spalt like transcription factor 4 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:19476507 1619916 Sall4 spalt like transcription factor 4 gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:18781635 1619916 Sall4 spalt like transcription factor 4 gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20141003 MGI PMID:19476507 1619916 Sall4 spalt like transcription factor 4 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:18781635 1619916 Sall4 spalt like transcription factor 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18781635 1619916 Sall4 spalt like transcription factor 4 gene MP:0001714 absent trophoblast giant cells IAGP N RGD:5509061 20141003 MGI PMID:17060609 1619916 Sall4 spalt like transcription factor 4 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17060609 1619916 Sall4 spalt like transcription factor 4 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18781635 1619916 Sall4 spalt like transcription factor 4 gene MP:0001849 ear inflammation IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17557835 1619916 Sall4 spalt like transcription factor 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19476507 1619916 Sall4 spalt like transcription factor 4 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:18781635 1619916 Sall4 spalt like transcription factor 4 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17060609 1619916 Sall4 spalt like transcription factor 4 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:17060609 1619916 Sall4 spalt like transcription factor 4 gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0003129 persistent cloaca IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0003130 anal atresia IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0003315 abnormal perineum morphology IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0003695 delayed blastocyst hatching from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:19476507 1619916 Sall4 spalt like transcription factor 4 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:18781635 1619916 Sall4 spalt like transcription factor 4 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:18781635 1619916 Sall4 spalt like transcription factor 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18781635 1619916 Sall4 spalt like transcription factor 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18818376 1619916 Sall4 spalt like transcription factor 4 gene MP:0004032 abnormal interventricular groove morphology IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0004638 elongated metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0004838 abnormal neural fold elevation formation IAGP N RGD:5509061 20141003 MGI PMID:18818376 1619916 Sall4 spalt like transcription factor 4 gene MP:0005034 abnormal anus morphology IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19476507 1619916 Sall4 spalt like transcription factor 4 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0009052 anal stenosis IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0009053 abnormal anal canal morphology IAGP N RGD:5509061 20141003 MGI PMID:19476507 1619916 Sall4 spalt like transcription factor 4 gene MP:0009098 anovaginal fistula IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:18781635 1619916 Sall4 spalt like transcription factor 4 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:18781635 1619916 Sall4 spalt like transcription factor 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0010432 common ventricle IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20150305 MGI PMID:18818376 1619916 Sall4 spalt like transcription factor 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17557835 1619916 Sall4 spalt like transcription factor 4 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19350679 1619916 Sall4 spalt like transcription factor 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17060609 1619916 Sall4 spalt like transcription factor 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18781635 1619916 Sall4 spalt like transcription factor 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19476507 1619916 Sall4 spalt like transcription factor 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18818376 1619916 Sall4 spalt like transcription factor 4 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18781635 1619916 Sall4 spalt like transcription factor 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18818376 1619916 Sall4 spalt like transcription factor 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19476507 1619916 Sall4 spalt like transcription factor 4 gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:19476507 1619916 Sall4 spalt like transcription factor 4 gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:18781635 1619916 Sall4 spalt like transcription factor 4 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:16790473 1619916 Sall4 spalt like transcription factor 4 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:19476507 1619916 Sall4 spalt like transcription factor 4 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18818376 1619916 Sall4 spalt like transcription factor 4 gene MP:0012739 abnormal anterior primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:18781635 1619916 Sall4 spalt like transcription factor 4 gene MP:0013167 abnormal hindlimb bud morphology IAGP N RGD:5509061 20150528 MGI PMID:16380715 1619916 Sall4 spalt like transcription factor 4 gene MP:0030410 middle ear effusion IAGP N RGD:5509061 20171207 MGI PMID:17216607 1619916 Sall4 spalt like transcription factor 4 gene MP:0030862 absent triquetrum IAGP N RGD:5509061 20181101 MGI PMID:17216607 1619917 Cul4a cullin 4A gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200514 MGI 1619917 Cul4a cullin 4A gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19430492 1619917 Cul4a cullin 4A gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1619917 Cul4a cullin 4A gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240627 MGI 1619917 Cul4a cullin 4A gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0002227 abnormal spleen capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20240523 MGI 1619917 Cul4a cullin 4A gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19430492 1619917 Cul4a cullin 4A gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:19430492 1619917 Cul4a cullin 4A gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:19481525 1619917 Cul4a cullin 4A gene MP:0004504 decreased incidence of tumors by UV induction IAGP N RGD:5509061 20141003 MGI PMID:19481525 1619917 Cul4a cullin 4A gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:19430492 1619917 Cul4a cullin 4A gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20201022 MGI 1619917 Cul4a cullin 4A gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20141003 MGI PMID:19430492 1619917 Cul4a cullin 4A gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:19481525 1619917 Cul4a cullin 4A gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:19430492 1619917 Cul4a cullin 4A gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:19430492 1619917 Cul4a cullin 4A gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20200514 MGI 1619917 Cul4a cullin 4A gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0009455 enhanced cued conditioning behavior IEA N RGD:5509061 20240523 MGI 1619917 Cul4a cullin 4A gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20190718 MGI PMID:19430492 1619917 Cul4a cullin 4A gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20200514 MGI 1619917 Cul4a cullin 4A gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0014078 small intestinal villus atrophy IAGP N RGD:5509061 20160310 MGI PMID:18339895 1619917 Cul4a cullin 4A gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:21291880 1619917 Cul4a cullin 4A gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:19430492 1619919 Pdxdc1 pyridoxal-dependent decarboxylase domain containing 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220519 MGI 1619919 Pdxdc1 pyridoxal-dependent decarboxylase domain containing 1 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20220519 MGI 1619919 Pdxdc1 pyridoxal-dependent decarboxylase domain containing 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20201022 MGI 1619919 Pdxdc1 pyridoxal-dependent decarboxylase domain containing 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1619919 Pdxdc1 pyridoxal-dependent decarboxylase domain containing 1 gene MP:0020422 decreased freezing behavior IEA N RGD:5509061 20200514 MGI 1619922 Dbr1 debranching RNA lariats 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1619922 Dbr1 debranching RNA lariats 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20160602 MGI PMID:25957684 1619922 Dbr1 debranching RNA lariats 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20160602 MGI PMID:25957684 1619922 Dbr1 debranching RNA lariats 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1619922 Dbr1 debranching RNA lariats 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619922 Dbr1 debranching RNA lariats 1 gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20181227 MGI 1619922 Dbr1 debranching RNA lariats 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1619923 Srrt serrate RNA effector molecule homolog (Arabidopsis) gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19632182 1619923 Srrt serrate RNA effector molecule homolog (Arabidopsis) gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18086880 1619923 Srrt serrate RNA effector molecule homolog (Arabidopsis) gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:18086880 1619923 Srrt serrate RNA effector molecule homolog (Arabidopsis) gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:19632182 1619923 Srrt serrate RNA effector molecule homolog (Arabidopsis) gene MP:0009322 increased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19632182 1619923 Srrt serrate RNA effector molecule homolog (Arabidopsis) gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18086880 1619923 Srrt serrate RNA effector molecule homolog (Arabidopsis) gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:18086880 1619924 Srbd1 S1 RNA binding domain 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 1619924 Srbd1 S1 RNA binding domain 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20210128 MGI 1619924 Srbd1 S1 RNA binding domain 1 gene MP:0001523 impaired righting response IEA N RGD:5509061 20210128 MGI 1619924 Srbd1 S1 RNA binding domain 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210520 MGI 1619924 Srbd1 S1 RNA binding domain 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20231207 MGI 1619924 Srbd1 S1 RNA binding domain 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619924 Srbd1 S1 RNA binding domain 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21282641 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:21071672 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:21282641 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:21282641 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:21071672 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:21421844 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21421844 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:21421844 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21071672 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21282641 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21421844 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21071672 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21421844 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21282641 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21421844 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21421844 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21071672 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:21071672 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:21421844 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:21071672 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:21282641 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0004171 abnormal pallium development IAGP N RGD:5509061 20141003 MGI PMID:21421844 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21071672 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21282641 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21421844 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23918385 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21421844 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0006088 abnormal blood-cerebrospinal fluid barrier function IAGP N RGD:5509061 20141003 MGI PMID:21421844 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:21282641 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:21421844 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:21282641 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21421844 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21282641 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21421844 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21071672 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0012732 abnormal perineural vascular plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:21071672 1619926 Adgra2 adhesion G protein-coupled receptor A2 gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:21421844 1619932 Micu3 mitochondrial calcium uptake family, member 3 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1619932 Micu3 mitochondrial calcium uptake family, member 3 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210128 MGI 1619932 Micu3 mitochondrial calcium uptake family, member 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220519 MGI 1619932 Micu3 mitochondrial calcium uptake family, member 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210520 MGI 1619934 Nkrf NF-kappaB repressing factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16354699 1619943 Exoc6b exocyst complex component 6B gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230119 MGI 1619943 Exoc6b exocyst complex component 6B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1619944 Vmp1 vacuole membrane protein 1 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:31526472 1619944 Vmp1 vacuole membrane protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:31526472 1619944 Vmp1 vacuole membrane protein 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20200310 MGI PMID:31526472 1619944 Vmp1 vacuole membrane protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:31526472 1619944 Vmp1 vacuole membrane protein 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:31526472 1619944 Vmp1 vacuole membrane protein 1 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20200310 MGI PMID:31526472 1619946 Dipk2b divergent protein kinase domain 2B gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1619946 Dipk2b divergent protein kinase domain 2B gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1619946 Dipk2b divergent protein kinase domain 2B gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1619946 Dipk2b divergent protein kinase domain 2B gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1619946 Dipk2b divergent protein kinase domain 2B gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 1619946 Dipk2b divergent protein kinase domain 2B gene MP:0009709 hydrometra IEA N RGD:5509061 20210128 MGI 1619946 Dipk2b divergent protein kinase domain 2B gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1619947 Tdrd9 tudor domain containing 9 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:20059948 1619947 Tdrd9 tudor domain containing 9 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:20059948 1619947 Tdrd9 tudor domain containing 9 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:20059948 1619947 Tdrd9 tudor domain containing 9 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:20059948 1619947 Tdrd9 tudor domain containing 9 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20200310 MGI PMID:20059948 1619947 Tdrd9 tudor domain containing 9 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20200310 MGI PMID:20059948 1619947 Tdrd9 tudor domain containing 9 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:20059948 1619947 Tdrd9 tudor domain containing 9 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20200310 MGI PMID:20059948 1619947 Tdrd9 tudor domain containing 9 gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20200310 MGI PMID:20059948 1619947 Tdrd9 tudor domain containing 9 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20200310 MGI PMID:20059948 1619947 Tdrd9 tudor domain containing 9 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:20059948 1619950 Ptchd3 patched domain containing 3 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1619950 Ptchd3 patched domain containing 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1619957 Ocstamp osteoclast stimulatory transmembrane protein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1619957 Ocstamp osteoclast stimulatory transmembrane protein gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20160825 MGI PMID:26042409 1619957 Ocstamp osteoclast stimulatory transmembrane protein gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160421 MGI 1619959 Nipsnap3a nipsnap homolog 3A gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20201231 MGI 1619961 Bpifa3 BPI fold containing family A, member 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1619964 Cimip4 ciliary microtubule inner protein 4 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210708 MGI PMID:32561905 1619967 Cldn34b2 claudin 34B2 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 1619968 1700034J05Rik RIKEN cDNA 1700034J05 gene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1619969 Itpripl1 inositol 1,4,5-triphosphate receptor interacting protein-like 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20240530 MGI PMID:38614099 1619969 Itpripl1 inositol 1,4,5-triphosphate receptor interacting protein-like 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240530 MGI PMID:38614099 1619970 Slc25a31 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 31 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17681941 1619970 Slc25a31 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 31 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17681941 1619970 Slc25a31 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 31 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17681941 1619970 Slc25a31 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 31 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17681941 1619970 Slc25a31 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 31 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17681941 1619970 Slc25a31 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 31 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:17681941 1619972 Pradc1 protease-associated domain containing 1 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20141003 MGI 1619977 Tmem68 transmembrane protein 68 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20200310 MGI 1619977 Tmem68 transmembrane protein 68 gene MP:0001258 decreased body length IAGP N RGD:5509061 20230928 MGI PMID:37648867 1619977 Tmem68 transmembrane protein 68 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230928 MGI PMID:37648867 1619977 Tmem68 transmembrane protein 68 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230928 MGI PMID:37648867 1619977 Tmem68 transmembrane protein 68 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20230928 MGI PMID:37648867 1619977 Tmem68 transmembrane protein 68 gene MP:0005316 abnormal response to tactile stimuli IEA N RGD:5509061 20200310 MGI 1619977 Tmem68 transmembrane protein 68 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20230928 MGI PMID:37648867 1619977 Tmem68 transmembrane protein 68 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20200310 MGI 1619977 Tmem68 transmembrane protein 68 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20230928 MGI PMID:37648867 1619977 Tmem68 transmembrane protein 68 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20230928 MGI PMID:37648867 1619977 Tmem68 transmembrane protein 68 gene MP:0010951 abnormal lipid oxidation IAGP N RGD:5509061 20230928 MGI PMID:37648867 1619977 Tmem68 transmembrane protein 68 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20230928 MGI PMID:37648867 1619977 Tmem68 transmembrane protein 68 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20230928 MGI PMID:37648867 1619978 Entpd8 ectonucleoside triphosphate diphosphohydrolase 8 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200310 MGI 1619978 Entpd8 ectonucleoside triphosphate diphosphohydrolase 8 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200310 MGI 1619978 Entpd8 ectonucleoside triphosphate diphosphohydrolase 8 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20240523 MGI PMID:34548395 1619978 Entpd8 ectonucleoside triphosphate diphosphohydrolase 8 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20240523 MGI PMID:34548395 1619978 Entpd8 ectonucleoside triphosphate diphosphohydrolase 8 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20240523 MGI PMID:34548395 1619978 Entpd8 ectonucleoside triphosphate diphosphohydrolase 8 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20240523 MGI PMID:34548395 1619978 Entpd8 ectonucleoside triphosphate diphosphohydrolase 8 gene MP:0013296 abnormal susceptibility to induced colitis IAGP N RGD:5509061 20240523 MGI PMID:34548395 1619979 Pigx phosphatidylinositol glycan anchor biosynthesis, class X gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1619979 Pigx phosphatidylinositol glycan anchor biosynthesis, class X gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20230601 MGI 1619980 Sapcd2 suppressor APC domain containing 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15567712 1619981 Anks4b ankyrin repeat and sterile alpha motif domain containing 4B gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20160804 MGI 1619984 Cnpy3 canopy FGF signaling regulator 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17998391 1619984 Cnpy3 canopy FGF signaling regulator 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17998391 1619984 Cnpy3 canopy FGF signaling regulator 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17998391 1619984 Cnpy3 canopy FGF signaling regulator 3 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17998391 1619984 Cnpy3 canopy FGF signaling regulator 3 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17998391 1619984 Cnpy3 canopy FGF signaling regulator 3 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17998391 1619984 Cnpy3 canopy FGF signaling regulator 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17998391 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0003707 increased cell nucleus count IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0008805 decreased circulating amylase level IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619985 Trmu tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20200310 MGI PMID:27689697 1619987 Cyb5r1 cytochrome b5 reductase 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20240307 MGI PMID:37572089 1619988 Btbd17 BTB domain containing 17 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1619988 Btbd17 BTB domain containing 17 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1619988 Btbd17 BTB domain containing 17 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 1619988 Btbd17 BTB domain containing 17 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1619988 Btbd17 BTB domain containing 17 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 1619988 Btbd17 BTB domain containing 17 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210520 MGI 1619988 Btbd17 BTB domain containing 17 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1619988 Btbd17 BTB domain containing 17 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1619988 Btbd17 BTB domain containing 17 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210826 MGI 1619988 Btbd17 BTB domain containing 17 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 1619988 Btbd17 BTB domain containing 17 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210128 MGI 1619991 Ggnbp1 gametogenetin binding protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20210513 MGI PMID:32139124 1619991 Ggnbp1 gametogenetin binding protein 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20210513 MGI PMID:32139124 1619991 Ggnbp1 gametogenetin binding protein 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210513 MGI PMID:32139124 1619991 Ggnbp1 gametogenetin binding protein 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20210513 MGI PMID:32139124 1619991 Ggnbp1 gametogenetin binding protein 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210513 MGI PMID:32139124 1619991 Ggnbp1 gametogenetin binding protein 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20210513 MGI PMID:32139124 1619991 Ggnbp1 gametogenetin binding protein 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210513 MGI PMID:32139124 1619991 Ggnbp1 gametogenetin binding protein 1 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20210513 MGI PMID:32139124 1619991 Ggnbp1 gametogenetin binding protein 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20210513 MGI PMID:32139124 1619992 Dclk2 doublecortin-like kinase 2 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20200310 MGI PMID:19342486 1619992 Dclk2 doublecortin-like kinase 2 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20200310 MGI PMID:19342486 1619992 Dclk2 doublecortin-like kinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19342486 1619992 Dclk2 doublecortin-like kinase 2 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:19342486 1619992 Dclk2 doublecortin-like kinase 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:19342486 1619992 Dclk2 doublecortin-like kinase 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220811 MGI 1619992 Dclk2 doublecortin-like kinase 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20200310 MGI PMID:19342486 1619992 Dclk2 doublecortin-like kinase 2 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20200310 MGI PMID:19342486 1619992 Dclk2 doublecortin-like kinase 2 gene MP:0008262 abnormal hippocampus region morphology IAGP N RGD:5509061 20200310 MGI PMID:19342486 1619992 Dclk2 doublecortin-like kinase 2 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20200310 MGI PMID:19342486 1619992 Dclk2 doublecortin-like kinase 2 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20200310 MGI PMID:19342486 1619992 Dclk2 doublecortin-like kinase 2 gene MP:0008285 abnormal hippocampus granule cell layer IAGP N RGD:5509061 20200310 MGI PMID:19342486 1619992 Dclk2 doublecortin-like kinase 2 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20200310 MGI PMID:19342486 1619992 Dclk2 doublecortin-like kinase 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1619992 Dclk2 doublecortin-like kinase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19342486 1619995 Cgn cingulin gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:22946046 1619995 Cgn cingulin gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20160811 MGI 1619995 Cgn cingulin gene MP:0001575 cyanosis IEA N RGD:5509061 20210520 MGI 1619995 Cgn cingulin gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160421 MGI 1619995 Cgn cingulin gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1619995 Cgn cingulin gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20160811 MGI 1619995 Cgn cingulin gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20160811 MGI 1619995 Cgn cingulin gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22946046 1619995 Cgn cingulin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20200310 MGI 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0000745 tremors IEA N RGD:5509061 20200310 MGI 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20200310 MGI PMID:27170476 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20201022 MGI 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20200310 MGI PMID:27170476 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200310 MGI PMID:27170476 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:27170476 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200310 MGI PMID:27170476 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0006110 ventricular fibrillation IAGP N RGD:5509061 20200310 MGI PMID:27170476 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20201231 MGI 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20200310 MGI PMID:27170476 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20200310 MGI PMID:27170476 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:27170476 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20200310 MGI 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1619996 Nos1ap nitric oxide synthase 1 (neuronal) adaptor protein gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20200310 MGI PMID:27170476 1620003 Tmco2 transmembrane and coiled-coil domains 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1620006 Prss56 serine protease 56 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20170504 MGI 1620006 Prss56 serine protease 56 gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20141003 MGI PMID:21532570 1620006 Prss56 serine protease 56 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1620006 Prss56 serine protease 56 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1620006 Prss56 serine protease 56 gene MP:0002697 abnormal eye size IAGP N RGD:5509061 20141003 MGI PMID:21532570 1620006 Prss56 serine protease 56 gene MP:0002698 abnormal sclera morphology IAGP N RGD:5509061 20141003 MGI PMID:21532570 1620006 Prss56 serine protease 56 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:21532570 1620006 Prss56 serine protease 56 gene MP:0004223 hypoplastic trabecular meshwork IAGP N RGD:5509061 20141003 MGI PMID:21532570 1620006 Prss56 serine protease 56 gene MP:0005098 abnormal optic choroid morphology IAGP N RGD:5509061 20141003 MGI PMID:21532570 1620006 Prss56 serine protease 56 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:21532570 1620006 Prss56 serine protease 56 gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20141003 MGI PMID:21532570 1620006 Prss56 serine protease 56 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21532570 1620006 Prss56 serine protease 56 gene MP:0009829 enlarged eye anterior chamber IAGP N RGD:5509061 20141003 MGI PMID:21532570 1620006 Prss56 serine protease 56 gene MP:0010081 posterior microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:21532570 1620007 Teshl testicular germ cell expressed HSF2 interacting lncRNA gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20221201 MGI PMID:34108217 1620007 Teshl testicular germ cell expressed HSF2 interacting lncRNA gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20221201 MGI PMID:34108217 1620012 Spmip3 sperm associated microtubule inner protein 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1620019 Cgnl1 cingulin-like 1 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IEA N RGD:5509061 20230720 MGI 1620019 Cgnl1 cingulin-like 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1620019 Cgnl1 cingulin-like 1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1620019 Cgnl1 cingulin-like 1 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 1620019 Cgnl1 cingulin-like 1 gene MP:0005407 hyperalgesia IEA N RGD:5509061 20230720 MGI 1620019 Cgnl1 cingulin-like 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1620020 Inka1 inka box actin regulator 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20175189 1620020 Inka1 inka box actin regulator 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:20175189 1620020 Inka1 inka box actin regulator 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20175189 1620021 Fdx2 ferredoxin 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1620021 Fdx2 ferredoxin 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1620021 Fdx2 ferredoxin 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1620021 Fdx2 ferredoxin 2 gene MP:0001586 abnormal erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1620021 Fdx2 ferredoxin 2 gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20210520 MGI 1620021 Fdx2 ferredoxin 2 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 1620021 Fdx2 ferredoxin 2 gene MP:0004002 abnormal jejunum morphology IEA N RGD:5509061 20210520 MGI 1620021 Fdx2 ferredoxin 2 gene MP:0004857 abnormal heart weight IEA N RGD:5509061 20211021 MGI 1620021 Fdx2 ferredoxin 2 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 1620021 Fdx2 ferredoxin 2 gene MP:0005563 abnormal hemoglobin content IEA N RGD:5509061 20211021 MGI 1620021 Fdx2 ferredoxin 2 gene MP:0012360 abnormal large unstained cell number IEA N RGD:5509061 20211021 MGI 1620024 Stx19 syntaxin 19 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 1620024 Stx19 syntaxin 19 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20220519 MGI 1620024 Stx19 syntaxin 19 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210826 MGI 1620024 Stx19 syntaxin 19 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1620026 Apool apolipoprotein O-like gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210520 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20210826 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20231207 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210826 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20220811 MGI 1620028 Entr1 endosome associated trafficking regulator 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210826 MGI 1620030 Naa16 N(alpha)-acetyltransferase 16, NatA auxiliary subunit gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1620030 Naa16 N(alpha)-acetyltransferase 16, NatA auxiliary subunit gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1620031 Eif4e3 eukaryotic translation initiation factor 4E member 3 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20200310 MGI 1620031 Eif4e3 eukaryotic translation initiation factor 4E member 3 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20200310 MGI 1620031 Eif4e3 eukaryotic translation initiation factor 4E member 3 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20200310 MGI 1620031 Eif4e3 eukaryotic translation initiation factor 4E member 3 gene MP:0001406 abnormal gait IEA N RGD:5509061 20200310 MGI 1620031 Eif4e3 eukaryotic translation initiation factor 4E member 3 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20200310 MGI 1620031 Eif4e3 eukaryotic translation initiation factor 4E member 3 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200310 MGI 1620031 Eif4e3 eukaryotic translation initiation factor 4E member 3 gene MP:0005571 decreased lactate dehydrogenase level IEA N RGD:5509061 20200310 MGI 1620031 Eif4e3 eukaryotic translation initiation factor 4E member 3 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20200310 MGI 1620031 Eif4e3 eukaryotic translation initiation factor 4E member 3 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:24652767 1620035 Hmg20a high mobility group 20A gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1620035 Hmg20a high mobility group 20A gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1620035 Hmg20a high mobility group 20A gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1620035 Hmg20a high mobility group 20A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620037 Mrpl33 mitochondrial ribosomal protein L33 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620037 Mrpl33 mitochondrial ribosomal protein L33 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1620039 Rsph3b radial spoke 3B homolog (Chlamydomonas) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20221215 MGI 1620040 Rnf186 ring finger protein 186 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20191017 MGI PMID:27381925 1620040 Rnf186 ring finger protein 186 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20191017 MGI PMID:27381925 1620040 Rnf186 ring finger protein 186 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20191017 MGI PMID:27381925 1620040 Rnf186 ring finger protein 186 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20191017 MGI PMID:27381925 1620040 Rnf186 ring finger protein 186 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20191017 MGI PMID:27381925 1620040 Rnf186 ring finger protein 186 gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20191017 MGI PMID:27381925 1620040 Rnf186 ring finger protein 186 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20191017 MGI PMID:27381925 1620041 Fbxo25 F-box protein 25 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1620041 Fbxo25 F-box protein 25 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1620041 Fbxo25 F-box protein 25 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 1620041 Fbxo25 F-box protein 25 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1620041 Fbxo25 F-box protein 25 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1620041 Fbxo25 F-box protein 25 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1620041 Fbxo25 F-box protein 25 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1620041 Fbxo25 F-box protein 25 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1620041 Fbxo25 F-box protein 25 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210520 MGI 1620041 Fbxo25 F-box protein 25 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1620041 Fbxo25 F-box protein 25 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1620041 Fbxo25 F-box protein 25 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20210128 MGI 1620041 Fbxo25 F-box protein 25 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20221215 MGI 1620041 Fbxo25 F-box protein 25 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 1620041 Fbxo25 F-box protein 25 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210128 MGI 1620041 Fbxo25 F-box protein 25 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220811 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20201022 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210128 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0000552 abnormal radius morphology IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20201231 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0001340 abnormal eyelid morphology IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20201022 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20201022 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170504 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210128 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20201022 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005015 increased T cell number IEA N RGD:5509061 20160811 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20160811 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005108 abnormal ulna morphology IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005270 abnormal zygomatic bone morphology IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210520 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005298 abnormal clavicle morphology IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005478 decreased circulating thyroxine level IEA N RGD:5509061 20201022 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20201022 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20201022 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20201022 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20201022 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0008174 decreased follicular B cell number IEA N RGD:5509061 20201231 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20201231 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0008211 decreased mature B cell number IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0008215 decreased immature B cell number IEA N RGD:5509061 20201231 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0008524 increased plasmacytoid dendritic cell number IEA N RGD:5509061 20201231 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20201022 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0009923 decreased transitional stage T1 B cell number IEA N RGD:5509061 20201231 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20201022 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0010099 abnormal thoracic cage shape IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0012768 decreased KLRG1-positive NK cell number IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0013026 decreased Ly6C low monocyte number IEA N RGD:5509061 20170105 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210520 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0013417 decreased memory-marker gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0013429 decreased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0013436 increased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0013649 decreased CD11b-high dendritic cell number IEA N RGD:5509061 20201231 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0013763 increased T-helper cell number IEA N RGD:5509061 20201231 MGI 1620045 Duoxa2 dual oxidase maturation factor 2 gene MP:0013771 decreased effector memory T-helper cell number IEA N RGD:5509061 20201231 MGI 1620047 Osbpl1a oxysterol binding protein-like 1A gene MP:0001513 limb grasping IEA N RGD:5509061 20231207 MGI 1620051 Evc EvC ciliary complex subunit 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:23026747 1620051 Evc EvC ciliary complex subunit 1 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:23026747 1620051 Evc EvC ciliary complex subunit 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:23026747 1620051 Evc EvC ciliary complex subunit 1 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20141003 MGI PMID:23026747 1620051 Evc EvC ciliary complex subunit 1 gene MP:0004604 abnormal vertebral pedicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:23026747 1620051 Evc EvC ciliary complex subunit 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23026747 1620051 Evc EvC ciliary complex subunit 1 gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23026747 1620051 Evc EvC ciliary complex subunit 1 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:23026747 1620051 Evc EvC ciliary complex subunit 1 gene MP:0014107 premature chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:17660199 1620051 Evc EvC ciliary complex subunit 1 gene MP:0030447 abnormal presphenoid synchondrosis IAGP N RGD:5509061 20180111 MGI PMID:23026747 1620051 Evc EvC ciliary complex subunit 1 gene MP:0030876 abnormal costochondral joint morphology IAGP N RGD:5509061 20181101 MGI PMID:17660199 1620052 Nsa2 NSA2 ribosome biogenesis homolog gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1620052 Nsa2 NSA2 ribosome biogenesis homolog gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1620052 Nsa2 NSA2 ribosome biogenesis homolog gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1620052 Nsa2 NSA2 ribosome biogenesis homolog gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1620052 Nsa2 NSA2 ribosome biogenesis homolog gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620052 Nsa2 NSA2 ribosome biogenesis homolog gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1620052 Nsa2 NSA2 ribosome biogenesis homolog gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1620053 C1galt1c1 C1GALT1-specific chaperone 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:20439703 1620053 C1galt1c1 C1GALT1-specific chaperone 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:20439703 1620053 C1galt1c1 C1GALT1-specific chaperone 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:20439703 1620053 C1galt1c1 C1GALT1-specific chaperone 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:20439703 1620053 C1galt1c1 C1GALT1-specific chaperone 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:20439703 1620053 C1galt1c1 C1GALT1-specific chaperone 1 gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:20439703 1620053 C1galt1c1 C1GALT1-specific chaperone 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20439703 1620053 C1galt1c1 C1GALT1-specific chaperone 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20439703 1620053 C1galt1c1 C1GALT1-specific chaperone 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20439703 1620054 Rnf130 ring finger protein 130 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20240404 MGI PMID:36876496 1620054 Rnf130 ring finger protein 130 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20240404 MGI PMID:36876496 1620054 Rnf130 ring finger protein 130 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20240404 MGI PMID:36876496 1620054 Rnf130 ring finger protein 130 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240404 MGI PMID:36876496 1620055 Pxmp4 peroxisomal membrane protein 4 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20220428 MGI PMID:35169201 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:23696638 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20150416 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0002861 abnormal tail bud morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0002990 short ureter IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0003126 abnormal external female genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0003445 sirenomelia IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0003535 absent vagina IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0003537 hydrometrocolpos IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0003591 urethra atresia IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0003591 urethra atresia IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0003605 fused kidneys IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0003605 fused kidneys IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0004710 small notochord IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0004714 truncated notochord IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0005034 abnormal anus morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0005354 abnormal ilium morphology IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0008786 abnormal hindgut morphology IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0008787 abnormal tailgut morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0008999 absent anus IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0008999 absent anus IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0009084 blind uterus IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0009199 abnormal external male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0009204 absent external male genitalia IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0009204 absent external male genitalia IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0009211 absent external female genitalia IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0009211 absent external female genitalia IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0009252 absent urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0009252 absent urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20335472 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0009709 hydrometra IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:20335472 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0010115 abnormal embryonic cloaca morphology IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0010116 abnormal primitive urogenital sinus morphology IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0011298 ureter hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0011771 abnormal genital tubercle morphology IAGP N RGD:5509061 20141003 MGI PMID:23696638 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0011797 blind ureter IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0012182 abnormal presomitic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0012182 abnormal presomitic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:20145239 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0013217 abnormal posterior definitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:19701191 1620056 Dact1 dishevelled-binding antagonist of beta-catenin 1 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:20335472 1620057 Sqor sulfide quinone oxidoreductase gene MP:0002083 premature death IAGP N RGD:5509061 20211202 MGI PMID:32923620 1620057 Sqor sulfide quinone oxidoreductase gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20211202 MGI PMID:32923620 1620059 Fmnl1 formin-like 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20180322 MGI PMID:28348104 1620059 Fmnl1 formin-like 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20180322 MGI PMID:28348104 1620059 Fmnl1 formin-like 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20180322 MGI PMID:28348104 1620059 Fmnl1 formin-like 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20180322 MGI PMID:28348104 1620059 Fmnl1 formin-like 1 gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20180322 MGI PMID:28348104 1620059 Fmnl1 formin-like 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180322 MGI PMID:28348104 1620060 Ntn4 netrin 4 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210128 MGI 1620060 Ntn4 netrin 4 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22281059 1620060 Ntn4 netrin 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1620060 Ntn4 netrin 4 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22281059 1620060 Ntn4 netrin 4 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210128 MGI 1620060 Ntn4 netrin 4 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:22281059 1620060 Ntn4 netrin 4 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22281059 1620060 Ntn4 netrin 4 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:22281059 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20709292 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20709292 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:20709292 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:20709292 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:20709292 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20709292 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15340057 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:19218085 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20709292 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20709292 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:15340057 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20709292 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20709292 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15340057 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20709292 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15340057 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:19218085 1620061 Pglyrp2 peptidoglycan recognition protein 2 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20141003 MGI PMID:20709292 1620062 Dnajb7 DnaJ heat shock protein family (Hsp40) member B7 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1620062 Dnajb7 DnaJ heat shock protein family (Hsp40) member B7 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1620063 Noc3l NOC3 like DNA replication regulator gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:23886952 1620063 Noc3l NOC3 like DNA replication regulator gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20200310 MGI PMID:23886952 1620063 Noc3l NOC3 like DNA replication regulator gene MP:0003706 abnormal cell nucleus count IAGP N RGD:5509061 20200310 MGI PMID:23886952 1620063 Noc3l NOC3 like DNA replication regulator gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23886952 1620065 Get3 guided entry of tail-anchored proteins factor 3, ATPase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16797549 1620067 Trpc4ap transient receptor potential cation channel, subfamily C, member 4 associated protein gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20211021 MGI PMID:30765221 1620067 Trpc4ap transient receptor potential cation channel, subfamily C, member 4 associated protein gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20211021 MGI PMID:30765221 1620067 Trpc4ap transient receptor potential cation channel, subfamily C, member 4 associated protein gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20211021 MGI PMID:30765221 1620067 Trpc4ap transient receptor potential cation channel, subfamily C, member 4 associated protein gene MP:0005331 insulin resistance IAGP N RGD:5509061 20211021 MGI PMID:30765221 1620067 Trpc4ap transient receptor potential cation channel, subfamily C, member 4 associated protein gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20211021 MGI PMID:30765221 1620067 Trpc4ap transient receptor potential cation channel, subfamily C, member 4 associated protein gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20211021 MGI PMID:30765221 1620067 Trpc4ap transient receptor potential cation channel, subfamily C, member 4 associated protein gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20190124 MGI PMID:25340873 1620067 Trpc4ap transient receptor potential cation channel, subfamily C, member 4 associated protein gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20211021 MGI PMID:30765221 1620067 Trpc4ap transient receptor potential cation channel, subfamily C, member 4 associated protein gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20211021 MGI PMID:30765221 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0000601 small liver IEA N RGD:5509061 20230601 MGI 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220707 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20230601 MGI 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20230601 MGI 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0001506 limp posture IAGP N RGD:5509061 20141003 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:23716689 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20230601 MGI 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0002764 short tibia IEA N RGD:5509061 20230601 MGI 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20230601 MGI 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:23716689 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20230601 MGI 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0004930 small epididymis IEA N RGD:5509061 20230601 MGI 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20230601 MGI 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:12151530 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:23716689 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:23716689 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23716689 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0010734 abnormal paranode morphology IAGP N RGD:5509061 20150611 MGI PMID:20506478 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0011736 decreased urine ammonia level IAGP N RGD:5509061 20141003 MGI PMID:23716689 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20170921 MGI PMID:23716689 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220707 MGI PMID:11917099 1620070 Gal3st1 galactose-3-O-sulfotransferase 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220707 MGI PMID:11917099 1620074 Oaz3 ornithine decarboxylase antizyme 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19893612 1620074 Oaz3 ornithine decarboxylase antizyme 3 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:19893612 1620074 Oaz3 ornithine decarboxylase antizyme 3 gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:19893612 1620075 Ncald neurocalcin delta gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1620075 Ncald neurocalcin delta gene MP:0000774 decreased brain size IAGP N RGD:5509061 20191003 MGI PMID:30853885 1620075 Ncald neurocalcin delta gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20191003 MGI PMID:30853885 1620075 Ncald neurocalcin delta gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20191003 MGI PMID:30853885 1620075 Ncald neurocalcin delta gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20191003 MGI PMID:30853885 1620075 Ncald neurocalcin delta gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20191003 MGI PMID:30853885 1620075 Ncald neurocalcin delta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191003 MGI PMID:30853885 1620075 Ncald neurocalcin delta gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20201231 MGI 1620075 Ncald neurocalcin delta gene MP:0001399 hyperactivity IEA N RGD:5509061 20170105 MGI 1620075 Ncald neurocalcin delta gene MP:0001921 reduced fertility IAGP N RGD:5509061 20191003 MGI PMID:30853885 1620075 Ncald neurocalcin delta gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1620075 Ncald neurocalcin delta gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20191003 MGI PMID:30853885 1620075 Ncald neurocalcin delta gene MP:0002546 mydriasis IEA N RGD:5509061 20160421 MGI 1620075 Ncald neurocalcin delta gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20240523 MGI 1620075 Ncald neurocalcin delta gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 1620075 Ncald neurocalcin delta gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1620075 Ncald neurocalcin delta gene MP:0003063 increased coping response IEA N RGD:5509061 20240523 MGI 1620075 Ncald neurocalcin delta gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20191003 MGI PMID:30853885 1620075 Ncald neurocalcin delta gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20191003 MGI PMID:30853885 1620075 Ncald neurocalcin delta gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160421 MGI 1620075 Ncald neurocalcin delta gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201231 MGI 1620075 Ncald neurocalcin delta gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1620075 Ncald neurocalcin delta gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1620075 Ncald neurocalcin delta gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20191003 MGI PMID:30853885 1620075 Ncald neurocalcin delta gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23088492 1620075 Ncald neurocalcin delta gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20160421 MGI 1620075 Ncald neurocalcin delta gene MP:0008283 small hippocampus IAGP N RGD:5509061 20191003 MGI PMID:30853885 1620075 Ncald neurocalcin delta gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20191003 MGI PMID:30853885 1620075 Ncald neurocalcin delta gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20191003 MGI PMID:30853885 1620075 Ncald neurocalcin delta gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1620075 Ncald neurocalcin delta gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20160421 MGI 1620075 Ncald neurocalcin delta gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1620075 Ncald neurocalcin delta gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23088492 1620075 Ncald neurocalcin delta gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20201231 MGI 1620075 Ncald neurocalcin delta gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20191003 MGI PMID:30853885 1620075 Ncald neurocalcin delta gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1620075 Ncald neurocalcin delta gene MP:0030981 abnormal dentate gyrus subgranular zone morphology IAGP N RGD:5509061 20191017 MGI PMID:30853885 1620078 Cenpo centromere protein O gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1620078 Cenpo centromere protein O gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210128 MGI 1620078 Cenpo centromere protein O gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1620078 Cenpo centromere protein O gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1620078 Cenpo centromere protein O gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191128 MGI 1620078 Cenpo centromere protein O gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191128 MGI 1620078 Cenpo centromere protein O gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191128 MGI 1620078 Cenpo centromere protein O gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1620078 Cenpo centromere protein O gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1620078 Cenpo centromere protein O gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20160421 MGI 1620078 Cenpo centromere protein O gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1620078 Cenpo centromere protein O gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191128 MGI 1620078 Cenpo centromere protein O gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20211021 MGI 1620078 Cenpo centromere protein O gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1620078 Cenpo centromere protein O gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1620078 Cenpo centromere protein O gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1620078 Cenpo centromere protein O gene MP:0009331 absent primitive node IEA N RGD:5509061 20191128 MGI 1620078 Cenpo centromere protein O gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1620078 Cenpo centromere protein O gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620078 Cenpo centromere protein O gene MP:0012724 absent head fold IEA N RGD:5509061 20191128 MGI 1620078 Cenpo centromere protein O gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20160804 MGI 1620078 Cenpo centromere protein O gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1620079 Tada1 transcriptional adaptor 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 1620079 Tada1 transcriptional adaptor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620079 Tada1 transcriptional adaptor 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1620081 Med24 mediator complex subunit 24 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620081 Med24 mediator complex subunit 24 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620081 Med24 mediator complex subunit 24 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620081 Med24 mediator complex subunit 24 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620081 Med24 mediator complex subunit 24 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620081 Med24 mediator complex subunit 24 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620081 Med24 mediator complex subunit 24 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620081 Med24 mediator complex subunit 24 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620081 Med24 mediator complex subunit 24 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620081 Med24 mediator complex subunit 24 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620081 Med24 mediator complex subunit 24 gene MP:0004085 abnormal heartbeat IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620081 Med24 mediator complex subunit 24 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620081 Med24 mediator complex subunit 24 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620081 Med24 mediator complex subunit 24 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620081 Med24 mediator complex subunit 24 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620081 Med24 mediator complex subunit 24 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12093747 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20200310 MGI PMID:25834070 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:21462293 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:21462293 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:21462293 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20200310 MGI PMID:21262216 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20200310 MGI PMID:21262216 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:18835385 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:21462293 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:21262216 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20200310 MGI PMID:21262216 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0003057 abnormal epicardium morphology IAGP N RGD:5509061 20200310 MGI PMID:21462293 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0003190 fused synovial joints IAGP N RGD:5509061 20200310 MGI PMID:21262216 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0003578 absent ovary IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20200310 MGI PMID:16790474 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0005644 agonadal IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0006415 absent testes IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20200310 MGI PMID:16790474 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0009075 rudimentary Wolffian ducts IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0009075 rudimentary Wolffian ducts IAGP N RGD:5509061 20200310 MGI PMID:16790474 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20200310 MGI PMID:21262216 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0010406 common atrium IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20200310 MGI PMID:21262216 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20200310 MGI PMID:16790474 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20200310 MGI PMID:16790474 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0010986 abnormal mesonephric mesenchyme morphology IAGP N RGD:5509061 20200310 MGI PMID:16790474 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0010987 abnormal nephrogenic mesenchyme morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25834070 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:21462293 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25834070 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0011366 absent metanephros IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0011366 absent metanephros IAGP N RGD:5509061 20200310 MGI PMID:16790474 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20200310 MGI PMID:16790474 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0011387 absent metanephric mesenchyme IAGP N RGD:5509061 20200310 MGI PMID:16790474 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0011412 gonadal ridge hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:16223478 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0013164 abnormal forelimb bud morphology IAGP N RGD:5509061 20200310 MGI PMID:21462293 1620082 Osr1 odd-skipped related transcription factor 1 gene MP:0031587 abnormal pericardium development IAGP N RGD:5509061 20240229 MGI PMID:16223478 1620083 Nr2e3 nuclear receptor subfamily 2, group E, member 3 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:16110338 1620083 Nr2e3 nuclear receptor subfamily 2, group E, member 3 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16110338 1620083 Nr2e3 nuclear receptor subfamily 2, group E, member 3 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:10805811 1620083 Nr2e3 nuclear receptor subfamily 2, group E, member 3 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16110338 1620083 Nr2e3 nuclear receptor subfamily 2, group E, member 3 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18547563 1620083 Nr2e3 nuclear receptor subfamily 2, group E, member 3 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10805811 1620083 Nr2e3 nuclear receptor subfamily 2, group E, member 3 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10805811 1620083 Nr2e3 nuclear receptor subfamily 2, group E, member 3 gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:18763016 1620083 Nr2e3 nuclear receptor subfamily 2, group E, member 3 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:18763016 1620083 Nr2e3 nuclear receptor subfamily 2, group E, member 3 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:18763016 1620083 Nr2e3 nuclear receptor subfamily 2, group E, member 3 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:18763016 1620084 Insl5 insulin-like 5 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:22822165 1620084 Insl5 insulin-like 5 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:22822165 1620084 Insl5 insulin-like 5 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:22822165 1620084 Insl5 insulin-like 5 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:22822165 1620084 Insl5 insulin-like 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22822165 1620084 Insl5 insulin-like 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:22822165 1620084 Insl5 insulin-like 5 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:22822165 1620084 Insl5 insulin-like 5 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:22822165 1620084 Insl5 insulin-like 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23438439 1620084 Insl5 insulin-like 5 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22822165 1620084 Insl5 insulin-like 5 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22822165 1620084 Insl5 insulin-like 5 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:22822165 1620084 Insl5 insulin-like 5 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22822165 1620084 Insl5 insulin-like 5 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:22822165 1620085 Rhof ras homolog family member F (in filopodia) gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20210429 MGI PMID:25741038 1620085 Rhof ras homolog family member F (in filopodia) gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23359340 1620085 Rhof ras homolog family member F (in filopodia) gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20210429 MGI PMID:25741038 1620087 Zfp30 zinc finger protein 30 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210225 MGI PMID:32860515 1620087 Zfp30 zinc finger protein 30 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20210225 MGI PMID:32860515 1620087 Zfp30 zinc finger protein 30 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20210225 MGI PMID:32860515 1620088 Zfp185 zinc finger protein 185 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20240404 MGI PMID:36631535 1620094 Ybx1 Y box protein 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20200310 MGI PMID:17082189 1620094 Ybx1 Y box protein 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20200310 MGI PMID:15899865 1620094 Ybx1 Y box protein 1 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20200310 MGI PMID:17082189 1620094 Ybx1 Y box protein 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20200310 MGI PMID:17082189 1620094 Ybx1 Y box protein 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:15899865 1620094 Ybx1 Y box protein 1 gene MP:0000601 small liver IAGP N RGD:5509061 20200310 MGI PMID:17082189 1620094 Ybx1 Y box protein 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20200310 MGI PMID:17082189 1620094 Ybx1 Y box protein 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:15899865 1620094 Ybx1 Y box protein 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:16954378 1620094 Ybx1 Y box protein 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:17082189 1620094 Ybx1 Y box protein 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20200310 MGI PMID:17082189 1620094 Ybx1 Y box protein 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:15899865 1620094 Ybx1 Y box protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:15899865 1620094 Ybx1 Y box protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:16954378 1620094 Ybx1 Y box protein 1 gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:17082189 1620094 Ybx1 Y box protein 1 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:15899865 1620094 Ybx1 Y box protein 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20200310 MGI PMID:15899865 1620094 Ybx1 Y box protein 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:16954378 1620094 Ybx1 Y box protein 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:17082189 1620094 Ybx1 Y box protein 1 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20200310 MGI PMID:15899865 1620094 Ybx1 Y box protein 1 gene MP:0003717 pallor IAGP N RGD:5509061 20200310 MGI PMID:15899865 1620094 Ybx1 Y box protein 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20200310 MGI PMID:15899865 1620094 Ybx1 Y box protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:17082189 1620094 Ybx1 Y box protein 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200310 MGI PMID:16954378 1620094 Ybx1 Y box protein 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20200310 MGI PMID:15899865 1620094 Ybx1 Y box protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15899865 1620094 Ybx1 Y box protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16598782 1620094 Ybx1 Y box protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17082189 1620094 Ybx1 Y box protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16954378 1620094 Ybx1 Y box protein 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15899865 1620094 Ybx1 Y box protein 1 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16954378 1620094 Ybx1 Y box protein 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:15899865 1620094 Ybx1 Y box protein 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:17082189 1620095 Tcap titin-cap gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:20233748 1620095 Tcap titin-cap gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20233748 1620095 Tcap titin-cap gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21799151 1620095 Tcap titin-cap gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:20233748 1620095 Tcap titin-cap gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21799151 1620095 Tcap titin-cap gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21799151 1620095 Tcap titin-cap gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:21799151 1620095 Tcap titin-cap gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:21799151 1620095 Tcap titin-cap gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:21799151 1620095 Tcap titin-cap gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:20233748 1620095 Tcap titin-cap gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:20233748 1620095 Tcap titin-cap gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:20233748 1620096 T2 brachyury 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20150312 MGI PMID:7589801 1620096 T2 brachyury 2 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:7589801 1620096 T2 brachyury 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:7589801 1620096 T2 brachyury 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:7589801 1620096 T2 brachyury 2 gene MP:0000932 absent notochord IAGP N RGD:5509061 20150312 MGI PMID:7589801 1620096 T2 brachyury 2 gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:7589801 1620096 T2 brachyury 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7589801 1620096 T2 brachyury 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7589801 1620097 Sub1 SUB1 homolog, transcriptional regulator gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20200310 MGI PMID:27471272 1620097 Sub1 SUB1 homolog, transcriptional regulator gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20200310 MGI PMID:27471272 1620098 Polr1d polymerase (RNA) I polypeptide D gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20240613 MGI PMID:33022126 1620098 Polr1d polymerase (RNA) I polypeptide D gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20240926 MGI 1620098 Polr1d polymerase (RNA) I polypeptide D gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20240613 MGI PMID:33022126 1620098 Polr1d polymerase (RNA) I polypeptide D gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20191205 MGI 1620098 Polr1d polymerase (RNA) I polypeptide D gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20240613 MGI PMID:33022126 1620098 Polr1d polymerase (RNA) I polypeptide D gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20240613 MGI PMID:33022126 1620098 Polr1d polymerase (RNA) I polypeptide D gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1620098 Polr1d polymerase (RNA) I polypeptide D gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20240613 MGI PMID:33022126 1620098 Polr1d polymerase (RNA) I polypeptide D gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20191205 MGI 1620098 Polr1d polymerase (RNA) I polypeptide D gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620098 Polr1d polymerase (RNA) I polypeptide D gene MP:0012129 failure of blastocyst formation IAGP N RGD:5509061 20240613 MGI PMID:33022126 1620098 Polr1d polymerase (RNA) I polypeptide D gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20240613 MGI PMID:33022126 1620098 Polr1d polymerase (RNA) I polypeptide D gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1620098 Polr1d polymerase (RNA) I polypeptide D gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20240613 MGI PMID:33022126 1620099 Pja1 praja ring finger ubiquitin ligase 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1620099 Pja1 praja ring finger ubiquitin ligase 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 1620099 Pja1 praja ring finger ubiquitin ligase 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210128 MGI 1620099 Pja1 praja ring finger ubiquitin ligase 1 gene MP:0001304 cataract IEA N RGD:5509061 20190502 MGI 1620099 Pja1 praja ring finger ubiquitin ligase 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1620099 Pja1 praja ring finger ubiquitin ligase 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1620099 Pja1 praja ring finger ubiquitin ligase 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1620099 Pja1 praja ring finger ubiquitin ligase 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20160505 MGI 1620099 Pja1 praja ring finger ubiquitin ligase 1 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210128 MGI 1620100 Pirb paired Ig-like receptor B gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20200310 MGI PMID:12021780 1620100 Pirb paired Ig-like receptor B gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20200310 MGI PMID:16917027 1620100 Pirb paired Ig-like receptor B gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:12021780 1620100 Pirb paired Ig-like receptor B gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:12021780 1620100 Pirb paired Ig-like receptor B gene MP:0004752 decreased length of allograft survival IAGP N RGD:5509061 20210506 MGI PMID:32381589 1620100 Pirb paired Ig-like receptor B gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20200310 MGI PMID:12021780 1620100 Pirb paired Ig-like receptor B gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:12021780 1620100 Pirb paired Ig-like receptor B gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20200310 MGI PMID:12021780 1620100 Pirb paired Ig-like receptor B gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:12021780 1620100 Pirb paired Ig-like receptor B gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20240613 MGI PMID:12021780 1620105 Pim2 proviral integration site 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15199164 1620105 Pim2 proviral integration site 2 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:15199164 1620105 Pim2 proviral integration site 2 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:15199164 1620105 Pim2 proviral integration site 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 1620105 Pim2 proviral integration site 2 gene MP:0003133 increased early pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 1620105 Pim2 proviral integration site 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 1620105 Pim2 proviral integration site 2 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15199164 1620105 Pim2 proviral integration site 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15199164 1620105 Pim2 proviral integration site 2 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 1620105 Pim2 proviral integration site 2 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 1620105 Pim2 proviral integration site 2 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 1620105 Pim2 proviral integration site 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20465571 1620105 Pim2 proviral integration site 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15199164 1620106 Mov10 Mov10 RISC complex RNA helicase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 1620106 Mov10 Mov10 RISC complex RNA helicase gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20180510 MGI PMID:28662698 1620106 Mov10 Mov10 RISC complex RNA helicase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1620106 Mov10 Mov10 RISC complex RNA helicase gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20231207 MGI 1620106 Mov10 Mov10 RISC complex RNA helicase gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20180510 MGI PMID:28662698 1620106 Mov10 Mov10 RISC complex RNA helicase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1620106 Mov10 Mov10 RISC complex RNA helicase gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 1620106 Mov10 Mov10 RISC complex RNA helicase gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:28662698 1620106 Mov10 Mov10 RISC complex RNA helicase gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20240523 MGI 1620106 Mov10 Mov10 RISC complex RNA helicase gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:28662698 1620107 Morc1 microrchidia 1 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:26275923 1620107 Morc1 microrchidia 1 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:9826705 1620107 Morc1 microrchidia 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20200310 MGI PMID:9826705 1620107 Morc1 microrchidia 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:26275923 1620107 Morc1 microrchidia 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:9826705 1620107 Morc1 microrchidia 1 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20200310 MGI PMID:26275923 1620107 Morc1 microrchidia 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200310 MGI PMID:9826705 1620107 Morc1 microrchidia 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:9826705 1620107 Morc1 microrchidia 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20200310 MGI PMID:9826705 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20141003 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0010854 lung situs inversus IAGP N RGD:5509061 20141003 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20200227 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0030591 absent sperm fibrous sheath IAGP N RGD:5509061 20180621 MGI PMID:22396656 1620108 Mns1 meiosis-specific nuclear structural protein 1 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220324 MGI PMID:22396656 1620109 Il9 interleukin 9 gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11070175 1620109 Il9 interleukin 9 gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12150887 1620109 Il9 interleukin 9 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1620109 Il9 interleukin 9 gene MP:0000601 small liver IEA N RGD:5509061 20230119 MGI 1620109 Il9 interleukin 9 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1620109 Il9 interleukin 9 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1620109 Il9 interleukin 9 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 1620109 Il9 interleukin 9 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1620109 Il9 interleukin 9 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230601 MGI 1620109 Il9 interleukin 9 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 1620109 Il9 interleukin 9 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:12150887 1620109 Il9 interleukin 9 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:12150887 1620109 Il9 interleukin 9 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1620109 Il9 interleukin 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24138883 1620109 Il9 interleukin 9 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12150887 1620109 Il9 interleukin 9 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12150887 1620109 Il9 interleukin 9 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12150887 1620109 Il9 interleukin 9 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:11070175 1620109 Il9 interleukin 9 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:12150887 1620109 Il9 interleukin 9 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 1620109 Il9 interleukin 9 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1620109 Il9 interleukin 9 gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 1620109 Il9 interleukin 9 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16266865 1620109 Il9 interleukin 9 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11070175 1620109 Il9 interleukin 9 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12150887 1620109 Il9 interleukin 9 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12150887 1620109 Il9 interleukin 9 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12150887 1620109 Il9 interleukin 9 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:11070175 1620109 Il9 interleukin 9 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:11070175 1620109 Il9 interleukin 9 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:12150887 1620109 Il9 interleukin 9 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:24138883 1620109 Il9 interleukin 9 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11070175 1620109 Il9 interleukin 9 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:12150887 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17292824 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000424 retarded hair growth IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20141003 MGI PMID:21804564 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17292824 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20478530 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20150326 MGI PMID:21878202 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000599 enlarged liver IAGP N RGD:5509061 20150326 MGI PMID:21878202 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17292824 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001265 decreased body size IAGP N RGD:5509061 20150326 MGI PMID:21878202 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20150326 MGI PMID:21878202 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20150326 MGI PMID:21878202 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:18490708 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17292824 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:17292824 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0001923 reduced female fertility IEA N RGD:5509061 20111116 MGI 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16782029 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17292824 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002658 abnormal liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:21804564 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17292824 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20478530 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17292824 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20150326 MGI PMID:21878202 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17292824 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17292824 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20478530 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20478530 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20150326 MGI PMID:21878202 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003454 erythroderma IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10766741 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20478530 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10766741 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20478530 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20150326 MGI PMID:21878202 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0004974 decreased regulatory T cell number IEA N RGD:5509061 20111116 MGI 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235208 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16782029 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:14499113 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0005083 abnormal biliary tract morphology IAGP N RGD:5509061 20150326 MGI PMID:21878202 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12235208 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0005159 azoospermia IEA N RGD:5509061 20111116 MGI 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20478530 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20150326 MGI PMID:21878202 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20150326 MGI PMID:21878202 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17292824 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17292824 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17292824 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17292824 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14499113 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14499113 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14499113 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14499113 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235208 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235208 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235208 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16782029 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235208 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008253 absent megakaryocytes IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18490708 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:18490708 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:10766741 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:18490708 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:18490708 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:18490708 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:18606991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0009385 abnormal dermal pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0009387 abnormal epidermal pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19635861 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0011009 increased circulating glutamate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:20478530 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10766741 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10911991 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:10766741 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:10911992 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:17292824 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:23871670 1620111 Ikbkg inhibitor of kappaB kinase gamma gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:23871670 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:1591779 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:1591779 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12055243 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8808678 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:1591779 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0002403 abnormal pre-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1591779 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0003134 increased late pro-B cell number IAGP N RGD:5509061 20240404 MGI PMID:12055243 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1591779 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0004976 abnormal B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:1591779 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12055243 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:1591779 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8808678 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:12055243 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:1591779 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12055243 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:8808678 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12055243 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:8808678 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12055243 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:8808678 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:1591779 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:1591779 1620112 Igll1 immunoglobulin lambda-like polypeptide 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:1591779 1620113 Gtf2i general transcription factor II I gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:19109438 1620113 Gtf2i general transcription factor II I gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:19109438 1620113 Gtf2i general transcription factor II I gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19109438 1620113 Gtf2i general transcription factor II I gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620113 Gtf2i general transcription factor II I gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620113 Gtf2i general transcription factor II I gene MP:0000449 broad nasal bridge IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620113 Gtf2i general transcription factor II I gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:19109438 1620113 Gtf2i general transcription factor II I gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19109438 1620113 Gtf2i general transcription factor II I gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620113 Gtf2i general transcription factor II I gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19109438 1620113 Gtf2i general transcription factor II I gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620113 Gtf2i general transcription factor II I gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620113 Gtf2i general transcription factor II I gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19109438 1620113 Gtf2i general transcription factor II I gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620113 Gtf2i general transcription factor II I gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19109438 1620113 Gtf2i general transcription factor II I gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620113 Gtf2i general transcription factor II I gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620113 Gtf2i general transcription factor II I gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20161216 MGI PMID:27194223 1620113 Gtf2i general transcription factor II I gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620113 Gtf2i general transcription factor II I gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620113 Gtf2i general transcription factor II I gene MP:0003742 narrow head IAGP N RGD:5509061 20141003 MGI PMID:19109438 1620113 Gtf2i general transcription factor II I gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19109438 1620113 Gtf2i general transcription factor II I gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19109438 1620113 Gtf2i general transcription factor II I gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:19109438 1620113 Gtf2i general transcription factor II I gene MP:0004557 dilated allantois IAGP N RGD:5509061 20141003 MGI PMID:19109438 1620113 Gtf2i general transcription factor II I gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620113 Gtf2i general transcription factor II I gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:19109438 1620113 Gtf2i general transcription factor II I gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19109438 1620113 Gtf2i general transcription factor II I gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22578324 1620113 Gtf2i general transcription factor II I gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20161216 MGI PMID:27194223 1620113 Gtf2i general transcription factor II I gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620113 Gtf2i general transcription factor II I gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620113 Gtf2i general transcription factor II I gene MP:0011184 absent embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620113 Gtf2i general transcription factor II I gene MP:0011192 decreased embryonic epiblast cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20403157 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15277241 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20141003 MGI PMID:15277241 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12052898 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15277241 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15277241 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:15277241 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15277241 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15277241 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12052898 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:15277241 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12052898 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:15277241 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0002893 ketoaciduria IAGP N RGD:5509061 20141003 MGI PMID:12052898 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0002893 ketoaciduria IAGP N RGD:5509061 20141003 MGI PMID:14599561 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:15277241 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:12052898 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:15277241 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0003946 renal necrosis IAGP N RGD:5509061 20141003 MGI PMID:12052898 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:15277241 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12052898 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12052898 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15277241 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12052898 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:15277241 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:12052898 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:15277241 1620114 Gstz1 glutathione transferase zeta 1 (maleylacetoacetate isomerase) gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:12052898 1620115 Gstp1 glutathione S-transferase, pi 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:9560266 1620115 Gstp1 glutathione S-transferase, pi 1 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:9560266 1620116 Gstp2 glutathione S-transferase, pi 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:9560266 1620116 Gstp2 glutathione S-transferase, pi 2 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20200310 MGI PMID:9560266 1620119 Haspin histone H3 associated protein kinase gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20181108 MGI PMID:27389782 1620120 Ebf2 early B cell factor 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16326388 1620120 Ebf2 early B cell factor 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16326388 1620120 Ebf2 early B cell factor 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:14993187 1620120 Ebf2 early B cell factor 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17521568 1620120 Ebf2 early B cell factor 2 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:16774995 1620120 Ebf2 early B cell factor 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:16774995 1620120 Ebf2 early B cell factor 2 gene MP:0000867 abnormal cerebellum anterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:16774995 1620120 Ebf2 early B cell factor 2 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:16774995 1620120 Ebf2 early B cell factor 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:23035080 1620120 Ebf2 early B cell factor 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16326388 1620120 Ebf2 early B cell factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17521568 1620120 Ebf2 early B cell factor 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20210128 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16326388 1620120 Ebf2 early B cell factor 2 gene MP:0001752 abnormal hypothalamus secretion IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20230330 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20230330 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210520 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17521568 1620120 Ebf2 early B cell factor 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:14993187 1620120 Ebf2 early B cell factor 2 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:14993187 1620120 Ebf2 early B cell factor 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:16326388 1620120 Ebf2 early B cell factor 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16326388 1620120 Ebf2 early B cell factor 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20220519 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16326388 1620120 Ebf2 early B cell factor 2 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20210128 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16326388 1620120 Ebf2 early B cell factor 2 gene MP:0003900 shortened QT interval IEA N RGD:5509061 20240523 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0004853 abnormal ovary size IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:16326388 1620120 Ebf2 early B cell factor 2 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17521568 1620120 Ebf2 early B cell factor 2 gene MP:0005279 narcolepsy IAGP N RGD:5509061 20141003 MGI PMID:21435382 1620120 Ebf2 early B cell factor 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20240523 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17521568 1620120 Ebf2 early B cell factor 2 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23035080 1620120 Ebf2 early B cell factor 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:21435382 1620120 Ebf2 early B cell factor 2 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17521568 1620120 Ebf2 early B cell factor 2 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23035080 1620120 Ebf2 early B cell factor 2 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:12466206 1620120 Ebf2 early B cell factor 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21435382 1620120 Ebf2 early B cell factor 2 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16326388 1620120 Ebf2 early B cell factor 2 gene MP:0010571 shortened ST segment IEA N RGD:5509061 20211021 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14993187 1620120 Ebf2 early B cell factor 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20210128 MGI 1620120 Ebf2 early B cell factor 2 gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:23035080 1620120 Ebf2 early B cell factor 2 gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:14993187 1620120 Ebf2 early B cell factor 2 gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20220915 MGI PMID:16326388 1620120 Ebf2 early B cell factor 2 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:16326388 1620125 Adam26a ADAM metallopeptidase domain 26A gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20181227 MGI 1620125 Adam26a ADAM metallopeptidase domain 26A gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 1620125 Adam26a ADAM metallopeptidase domain 26A gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20181227 MGI 1620125 Adam26a ADAM metallopeptidase domain 26A gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20181227 MGI 1620125 Adam26a ADAM metallopeptidase domain 26A gene MP:0012125 decreased bronchoconstrictive response IEA N RGD:5509061 20201022 MGI 1620126 Dsg3 desmoglein 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9284099 1620126 Dsg3 desmoglein 3 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:9166409 1620126 Dsg3 desmoglein 3 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:9284099 1620126 Dsg3 desmoglein 3 gene MP:0000414 alopecia IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:9284099 1620126 Dsg3 desmoglein 3 gene MP:0000416 sparse hair IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:9166409 1620126 Dsg3 desmoglein 3 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:9166409 1620126 Dsg3 desmoglein 3 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:9284099 1620126 Dsg3 desmoglein 3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:9166409 1620126 Dsg3 desmoglein 3 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0001234 absent suprabasal layer IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9166409 1620126 Dsg3 desmoglein 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:9166409 1620126 Dsg3 desmoglein 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9166409 1620126 Dsg3 desmoglein 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9166409 1620126 Dsg3 desmoglein 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:9166409 1620126 Dsg3 desmoglein 3 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0002249 abnormal larynx morphology IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0002256 abnormal laryngeal cartilage morphology IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:8182278 1620126 Dsg3 desmoglein 3 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:9166409 1620126 Dsg3 desmoglein 3 gene MP:0003747 mouth mucosal ulcer IAGP N RGD:5509061 20141003 MGI PMID:9166409 1620126 Dsg3 desmoglein 3 gene MP:0003747 mouth mucosal ulcer IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:9166409 1620126 Dsg3 desmoglein 3 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:9284099 1620126 Dsg3 desmoglein 3 gene MP:0004241 acantholysis IAGP N RGD:5509061 20141003 MGI PMID:9166409 1620126 Dsg3 desmoglein 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0005114 premature hair loss IAGP N RGD:5509061 20141003 MGI PMID:9284099 1620126 Dsg3 desmoglein 3 gene MP:0005150 cachexia IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0009247 meteorism IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0009474 thick epidermis stratum spinosum IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0009598 thin epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:9284099 1620126 Dsg3 desmoglein 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:9166409 1620126 Dsg3 desmoglein 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0010371 abnormal epiglottis morphology IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9166409 1620126 Dsg3 desmoglein 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0012491 larynx stenosis IAGP N RGD:5509061 20191219 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0013752 stridor IAGP N RGD:5509061 20160616 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0030000 abnormal subglottis morphology IAGP N RGD:5509061 20160714 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0030001 subglottis stenosis IAGP N RGD:5509061 20160714 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0030520 oral mucosa blisters IAGP N RGD:5509061 20180118 MGI PMID:9284099 1620126 Dsg3 desmoglein 3 gene MP:0030533 abnormal snout skin morphology IAGP N RGD:5509061 20180118 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0030894 epiglottis hyperplasia IAGP N RGD:5509061 20191219 MGI PMID:25542773 1620126 Dsg3 desmoglein 3 gene MP:0031395 cutaneous mastocytosis IAGP N RGD:5509061 20220721 MGI PMID:8182278 1620128 Chic1 cysteine-rich hydrophobic domain 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1620128 Chic1 cysteine-rich hydrophobic domain 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1620240 Ctcfl CCCTC-binding factor like gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:20231363 1620240 Ctcfl CCCTC-binding factor like gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20231363 1620240 Ctcfl CCCTC-binding factor like gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:20231363 1620240 Ctcfl CCCTC-binding factor like gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20231363 1620240 Ctcfl CCCTC-binding factor like gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:20231363 1620240 Ctcfl CCCTC-binding factor like gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20231363 1620250 Fbxw7as1 F-box and WD-40 domain protein 7 antisense transcript 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16293765 1620250 Fbxw7as1 F-box and WD-40 domain protein 7 antisense transcript 1 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:16293765 1620250 Fbxw7as1 F-box and WD-40 domain protein 7 antisense transcript 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16293765 1620250 Fbxw7as1 F-box and WD-40 domain protein 7 antisense transcript 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16293765 1620250 Fbxw7as1 F-box and WD-40 domain protein 7 antisense transcript 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16293765 1620250 Fbxw7as1 F-box and WD-40 domain protein 7 antisense transcript 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20160331 MGI PMID:16293765 1620250 Fbxw7as1 F-box and WD-40 domain protein 7 antisense transcript 1 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16293765 1620250 Fbxw7as1 F-box and WD-40 domain protein 7 antisense transcript 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16293765 1620250 Fbxw7as1 F-box and WD-40 domain protein 7 antisense transcript 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:16293765 1620250 Fbxw7as1 F-box and WD-40 domain protein 7 antisense transcript 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:16293765 1620250 Fbxw7as1 F-box and WD-40 domain protein 7 antisense transcript 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16293765 1620250 Fbxw7as1 F-box and WD-40 domain protein 7 antisense transcript 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16293765 1620250 Fbxw7as1 F-box and WD-40 domain protein 7 antisense transcript 1 gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20141003 MGI PMID:16293765 1620251 Mymx myomixer, myoblast fusion factor gene MP:0000747 muscle weakness IAGP N RGD:5509061 20170706 MGI PMID:28569755 1620251 Mymx myomixer, myoblast fusion factor gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20170706 MGI PMID:28569755 1620251 Mymx myomixer, myoblast fusion factor gene MP:0001575 cyanosis IAGP N RGD:5509061 20170706 MGI PMID:28569755 1620251 Mymx myomixer, myoblast fusion factor gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20170706 MGI PMID:28569755 1620251 Mymx myomixer, myoblast fusion factor gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20170706 MGI PMID:28569755 1620251 Mymx myomixer, myoblast fusion factor gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20170706 MGI PMID:28569755 1620251 Mymx myomixer, myoblast fusion factor gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20170706 MGI PMID:28569755 1620251 Mymx myomixer, myoblast fusion factor gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20170706 MGI PMID:28569755 1620251 Mymx myomixer, myoblast fusion factor gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20170706 MGI PMID:28569755 1620251 Mymx myomixer, myoblast fusion factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170706 MGI PMID:28569745 1620251 Mymx myomixer, myoblast fusion factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170706 MGI PMID:28569755 1620251 Mymx myomixer, myoblast fusion factor gene MP:0012269 nuchal edema IAGP N RGD:5509061 20170706 MGI PMID:28569755 1620251 Mymx myomixer, myoblast fusion factor gene MP:0021206 abnormal limb muscle morphology IAGP N RGD:5509061 20221201 MGI PMID:28569755 1620251 Mymx myomixer, myoblast fusion factor gene MP:0030959 abnormal myoblast fusion IAGP N RGD:5509061 20190725 MGI PMID:28569755 1620254 Pinlyp phospholipase A2 inhibitor and LY6/PLAUR domain containing gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1620254 Pinlyp phospholipase A2 inhibitor and LY6/PLAUR domain containing gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20240530 MGI PMID:34969857 1620260 Cfap47 cilia and flagella associated protein 47 gene MP:0001340 abnormal eyelid morphology IEA N RGD:5509061 20240523 MGI 1620260 Cfap47 cilia and flagella associated protein 47 gene MP:0001925 male infertility IAGP N RGD:5509061 20210812 MGI PMID:33472045 1620260 Cfap47 cilia and flagella associated protein 47 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210812 MGI PMID:33472045 1620260 Cfap47 cilia and flagella associated protein 47 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1620260 Cfap47 cilia and flagella associated protein 47 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20240523 MGI 1620260 Cfap47 cilia and flagella associated protein 47 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210812 MGI PMID:33472045 1620260 Cfap47 cilia and flagella associated protein 47 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20210812 MGI PMID:33472045 1620260 Cfap47 cilia and flagella associated protein 47 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1620260 Cfap47 cilia and flagella associated protein 47 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20210812 MGI PMID:33472045 1620268 Ang6 angiogenin, ribonuclease A family, member 6 gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20231207 MGI 1620285 Zfp800 zinc finger protein 800 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20210701 MGI PMID:33653874 1620285 Zfp800 zinc finger protein 800 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20210701 MGI PMID:33653874 1620285 Zfp800 zinc finger protein 800 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20210701 MGI PMID:33653874 1620285 Zfp800 zinc finger protein 800 gene MP:0009181 decreased pancreatic delta cell number IAGP N RGD:5509061 20210701 MGI PMID:33653874 1620285 Zfp800 zinc finger protein 800 gene MP:0009186 decreased PP cell number IAGP N RGD:5509061 20210701 MGI PMID:33653874 1620285 Zfp800 zinc finger protein 800 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210701 MGI PMID:33653874 1620285 Zfp800 zinc finger protein 800 gene MP:0011932 abnormal endocrine pancreas development IAGP N RGD:5509061 20210701 MGI PMID:33653874 1620315 Prr19 proline rich 19 gene MP:0001925 male infertility IAGP N RGD:5509061 20201001 MGI PMID:32555348 1620315 Prr19 proline rich 19 gene MP:0001926 female infertility IAGP N RGD:5509061 20201001 MGI PMID:32555348 1620315 Prr19 proline rich 19 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20201001 MGI PMID:32555348 1620315 Prr19 proline rich 19 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20201001 MGI PMID:32555348 1620315 Prr19 proline rich 19 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20201001 MGI PMID:32555348 1620315 Prr19 proline rich 19 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20201001 MGI PMID:32555348 1620315 Prr19 proline rich 19 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20201001 MGI PMID:32555348 1620315 Prr19 proline rich 19 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20201001 MGI PMID:32555348 1620315 Prr19 proline rich 19 gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20201001 MGI PMID:32555348 1620315 Prr19 proline rich 19 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20201001 MGI PMID:32555348 1620337 Rfx8 regulatory factor X 8 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1620337 Rfx8 regulatory factor X 8 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1620338 Garin4 golgi associated RAB2 interactor family member 4 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240801 MGI PMID:38935810 1620338 Garin4 golgi associated RAB2 interactor family member 4 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20240801 MGI PMID:38935810 1620339 Rtl4 retrotransposon Gag like 4 gene MP:0001357 increased aggression towards humans IAGP N RGD:5509061 20180628 MGI PMID:26402067 1620339 Rtl4 retrotransposon Gag like 4 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20180628 MGI PMID:26402067 1620339 Rtl4 retrotransposon Gag like 4 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20180628 MGI PMID:26402067 1620339 Rtl4 retrotransposon Gag like 4 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20180628 MGI PMID:26402067 1620339 Rtl4 retrotransposon Gag like 4 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20180628 MGI PMID:26402067 1620339 Rtl4 retrotransposon Gag like 4 gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20180628 MGI PMID:26402067 1620339 Rtl4 retrotransposon Gag like 4 gene MP:0014114 abnormal cognition IAGP N RGD:5509061 20180628 MGI PMID:26402067 1620339 Rtl4 retrotransposon Gag like 4 gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:26402067 1620351 Or10ad1c olfactory receptor family 10 subfamily AD member 1C gene MP:0020852 abnormal olfactory behavior IAGP N RGD:5509061 20200917 MGI PMID:30643144 1620352 Fam186b family with sequence similarity 186, member B gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1620352 Fam186b family with sequence similarity 186, member B gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20240523 MGI 1620352 Fam186b family with sequence similarity 186, member B gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20231207 MGI 1620359 Xkr4 X-linked Kx blood group related 4 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1620359 Xkr4 X-linked Kx blood group related 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1620359 Xkr4 X-linked Kx blood group related 4 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210128 MGI 1620359 Xkr4 X-linked Kx blood group related 4 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1620360 BC037156 cDNA sequence BC037156 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1620362 Cbx6 chromobox 6 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20141003 MGI 1620362 Cbx6 chromobox 6 gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20150430 MGI 1620362 Cbx6 chromobox 6 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1620362 Cbx6 chromobox 6 gene MP:0002928 abnormal bile duct morphology IEA N RGD:5509061 20171228 MGI 1620362 Cbx6 chromobox 6 gene MP:0002947 increased hemangioma incidence IEA N RGD:5509061 20210930 MGI 1620362 Cbx6 chromobox 6 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20141003 MGI 1620362 Cbx6 chromobox 6 gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20171228 MGI 1620362 Cbx6 chromobox 6 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150108 MGI 1620362 Cbx6 chromobox 6 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20141003 MGI 1620362 Cbx6 chromobox 6 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1620362 Cbx6 chromobox 6 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20141003 MGI 1620362 Cbx6 chromobox 6 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1620362 Cbx6 chromobox 6 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20141003 MGI 1620362 Cbx6 chromobox 6 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1620362 Cbx6 chromobox 6 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 1620362 Cbx6 chromobox 6 gene MP:0009820 abnormal liver vasculature morphology IEA N RGD:5509061 20171228 MGI 1620362 Cbx6 chromobox 6 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20141003 MGI 1620362 Cbx6 chromobox 6 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20150108 MGI 1620362 Cbx6 chromobox 6 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20171228 MGI 1620362 Cbx6 chromobox 6 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1620362 Cbx6 chromobox 6 gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20171228 MGI 1620362 Cbx6 chromobox 6 gene MP:0013852 abnormal Mullerian duct topology IEA N RGD:5509061 20171228 MGI 1620362 Cbx6 chromobox 6 gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20171228 MGI 1620362 Cbx6 chromobox 6 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20171228 MGI 1620362 Cbx6 chromobox 6 gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20171228 MGI 1620362 Cbx6 chromobox 6 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20171228 MGI 1620362 Cbx6 chromobox 6 gene MP:0014021 heterochrony IEA N RGD:5509061 20171228 MGI 1620363 Gsdma3 gasdermin A3 gene MP:0000017 big ears IEA N RGD:5509061 20111116 MGI 1620363 Gsdma3 gasdermin A3 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1620363 Gsdma3 gasdermin A3 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:9434940 1620363 Gsdma3 gasdermin A3 gene MP:0000397 abnormal guard hair morphology IAGP N RGD:5509061 20141003 MGI PMID:12164921 1620363 Gsdma3 gasdermin A3 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12164921 1620363 Gsdma3 gasdermin A3 gene MP:0000414 alopecia IAGP N RGD:5509061 20151119 MGI PMID:22682752 1620363 Gsdma3 gasdermin A3 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:9434940 1620363 Gsdma3 gasdermin A3 gene MP:0000423 delayed hair regrowth IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:17572385 1620363 Gsdma3 gasdermin A3 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0000648 absent sebaceous gland IAGP N RGD:5509061 20151119 MGI PMID:22682752 1620363 Gsdma3 gasdermin A3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:15475261 1620363 Gsdma3 gasdermin A3 gene MP:0001194 dermatitis IEA N RGD:5509061 20141003 MGI 1620363 Gsdma3 gasdermin A3 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:12164921 1620363 Gsdma3 gasdermin A3 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:12164921 1620363 Gsdma3 gasdermin A3 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0001212 skin lesions IEA N RGD:5509061 20141003 MGI 1620363 Gsdma3 gasdermin A3 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9434940 1620363 Gsdma3 gasdermin A3 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:9434940 1620363 Gsdma3 gasdermin A3 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:9434940 1620363 Gsdma3 gasdermin A3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20111116 MGI 1620363 Gsdma3 gasdermin A3 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:12164921 1620363 Gsdma3 gasdermin A3 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:9434940 1620363 Gsdma3 gasdermin A3 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:15475261 1620363 Gsdma3 gasdermin A3 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:9434940 1620363 Gsdma3 gasdermin A3 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:15475261 1620363 Gsdma3 gasdermin A3 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:9434940 1620363 Gsdma3 gasdermin A3 gene MP:0002832 coarse hair IEA N RGD:5509061 20111116 MGI 1620363 Gsdma3 gasdermin A3 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1620363 Gsdma3 gasdermin A3 gene MP:0002881 long hair IEA N RGD:5509061 20111116 MGI 1620363 Gsdma3 gasdermin A3 gene MP:0003095 abnormal cornea stroma development IAGP N RGD:5509061 20141003 MGI PMID:9434940 1620363 Gsdma3 gasdermin A3 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:15475261 1620363 Gsdma3 gasdermin A3 gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20141003 MGI PMID:20977888 1620363 Gsdma3 gasdermin A3 gene MP:0003853 dry skin IEA N RGD:5509061 20141003 MGI 1620363 Gsdma3 gasdermin A3 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1620363 Gsdma3 gasdermin A3 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1620363 Gsdma3 gasdermin A3 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1620363 Gsdma3 gasdermin A3 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9434940 1620363 Gsdma3 gasdermin A3 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20141003 MGI PMID:17572385 1620363 Gsdma3 gasdermin A3 gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0009351 thin hair shaft IAGP N RGD:5509061 20141003 MGI PMID:20977888 1620363 Gsdma3 gasdermin A3 gene MP:0009600 hypergranulosis IAGP N RGD:5509061 20141003 MGI PMID:9434940 1620363 Gsdma3 gasdermin A3 gene MP:0009742 increased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:9434940 1620363 Gsdma3 gasdermin A3 gene MP:0009759 abnormal hair follicle bulge morphology IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0009859 eye opacity IEA N RGD:5509061 20141003 MGI 1620363 Gsdma3 gasdermin A3 gene MP:0010678 abnormal skin adnexa morphology IAGP N RGD:5509061 20141003 MGI PMID:22155111 1620363 Gsdma3 gasdermin A3 gene MP:0011585 decreased alkaline phosphatase activity IAGP N RGD:5509061 20151119 MGI PMID:22682752 1620363 Gsdma3 gasdermin A3 gene MP:0020859 disorganized cornea epithelium IAGP N RGD:5509061 20181101 MGI PMID:9434940 1620392 Sgpp2 sphingosine-1-phosphate phosphatase 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20170309 MGI PMID:27059959 1620392 Sgpp2 sphingosine-1-phosphate phosphatase 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20170309 MGI PMID:27059959 1620392 Sgpp2 sphingosine-1-phosphate phosphatase 2 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20170309 MGI PMID:27059959 1620392 Sgpp2 sphingosine-1-phosphate phosphatase 2 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20170309 MGI PMID:27059959 1620392 Sgpp2 sphingosine-1-phosphate phosphatase 2 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20170309 MGI PMID:27059959 1620392 Sgpp2 sphingosine-1-phosphate phosphatase 2 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20170309 MGI PMID:27059959 1620392 Sgpp2 sphingosine-1-phosphate phosphatase 2 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20170309 MGI PMID:27059959 1620392 Sgpp2 sphingosine-1-phosphate phosphatase 2 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20170309 MGI PMID:27059959 1620396 Neurl2 neuralized E3 ubiquitin protein ligase 2 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1620396 Neurl2 neuralized E3 ubiquitin protein ligase 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:14960280 1620396 Neurl2 neuralized E3 ubiquitin protein ligase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14960280 1620396 Neurl2 neuralized E3 ubiquitin protein ligase 2 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20170105 MGI 1620396 Neurl2 neuralized E3 ubiquitin protein ligase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18043734 1620396 Neurl2 neuralized E3 ubiquitin protein ligase 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1620396 Neurl2 neuralized E3 ubiquitin protein ligase 2 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220519 MGI 1620396 Neurl2 neuralized E3 ubiquitin protein ligase 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1620397 Iqgap3 IQ motif containing GTPase activating protein 3 gene MP:0002626 increased heart rate IEA N RGD:5509061 20231207 MGI 1620397 Iqgap3 IQ motif containing GTPase activating protein 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230119 MGI 1620399 Ccdc87 coiled-coil domain containing 87 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20190321 MGI PMID:29733332 1620399 Ccdc87 coiled-coil domain containing 87 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20190321 MGI PMID:29733332 1620399 Ccdc87 coiled-coil domain containing 87 gene MP:0001925 male infertility IAGP N RGD:5509061 20190321 MGI PMID:29733332 1620399 Ccdc87 coiled-coil domain containing 87 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20190321 MGI PMID:29733332 1620399 Ccdc87 coiled-coil domain containing 87 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20190321 MGI PMID:29733332 1620399 Ccdc87 coiled-coil domain containing 87 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20190321 MGI PMID:29733332 1620399 Ccdc87 coiled-coil domain containing 87 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20190321 MGI PMID:29733332 1620399 Ccdc87 coiled-coil domain containing 87 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20190321 MGI PMID:29733332 1620399 Ccdc87 coiled-coil domain containing 87 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220303 MGI PMID:29733332 1620403 Cdin1 CDAN1 interacting nuclease 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20210128 MGI 1620403 Cdin1 CDAN1 interacting nuclease 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1620403 Cdin1 CDAN1 interacting nuclease 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1620403 Cdin1 CDAN1 interacting nuclease 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1620403 Cdin1 CDAN1 interacting nuclease 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1620405 Flrt2 fibronectin leucine rich transmembrane protein 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:21350012 1620405 Flrt2 fibronectin leucine rich transmembrane protein 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21350012 1620405 Flrt2 fibronectin leucine rich transmembrane protein 2 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:21350012 1620405 Flrt2 fibronectin leucine rich transmembrane protein 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:21673655 1620405 Flrt2 fibronectin leucine rich transmembrane protein 2 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:21350012 1620405 Flrt2 fibronectin leucine rich transmembrane protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21350012 1620405 Flrt2 fibronectin leucine rich transmembrane protein 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21350012 1620405 Flrt2 fibronectin leucine rich transmembrane protein 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21350012 1620405 Flrt2 fibronectin leucine rich transmembrane protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21350012 1620405 Flrt2 fibronectin leucine rich transmembrane protein 2 gene MP:0031590 abnormal epicardium development IAGP N RGD:5509061 20240229 MGI PMID:21350012 1620406 Scn4b sodium channel, type IV, beta gene MP:0000745 tremors IEA N RGD:5509061 20181227 MGI 1620406 Scn4b sodium channel, type IV, beta gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 1620406 Scn4b sodium channel, type IV, beta gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20180628 MGI PMID:28243192 1620406 Scn4b sodium channel, type IV, beta gene MP:0003466 decreased single cell response threshold IAGP N RGD:5509061 20180628 MGI PMID:28243192 1620406 Scn4b sodium channel, type IV, beta gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20180628 MGI PMID:28243192 1620406 Scn4b sodium channel, type IV, beta gene MP:0030586 impaired behavioral response to amphetamine IAGP N RGD:5509061 20180628 MGI PMID:28243192 1620407 Map4k5 mitogen-activated protein kinase kinase kinase kinase 5 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1620407 Map4k5 mitogen-activated protein kinase kinase kinase kinase 5 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20190502 MGI 1620407 Map4k5 mitogen-activated protein kinase kinase kinase kinase 5 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1620407 Map4k5 mitogen-activated protein kinase kinase kinase kinase 5 gene MP:0003043 hypoalgesia IEA N RGD:5509061 20141003 MGI 1620407 Map4k5 mitogen-activated protein kinase kinase kinase kinase 5 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16914735 1620407 Map4k5 mitogen-activated protein kinase kinase kinase kinase 5 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16914735 1620407 Map4k5 mitogen-activated protein kinase kinase kinase kinase 5 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20141003 MGI 1620407 Map4k5 mitogen-activated protein kinase kinase kinase kinase 5 gene MP:0008499 increased IgG1 level IEA N RGD:5509061 20141003 MGI 1620423 Zbtb42 zinc finger and BTB domain containing 42 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1620423 Zbtb42 zinc finger and BTB domain containing 42 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1620427 4921509C19Rik RIKEN cDNA 4921509C19 gene gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1620427 4921509C19Rik RIKEN cDNA 4921509C19 gene gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1620427 4921509C19Rik RIKEN cDNA 4921509C19 gene gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220811 MGI 1620427 4921509C19Rik RIKEN cDNA 4921509C19 gene gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 1620429 Med19 mediator complex subunit 19 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0000603 pale liver IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0001260 increased body weight IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0006320 abnormal interscapular fat pad morphology IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0009132 abnormal white fat cell size IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620429 Med19 mediator complex subunit 19 gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0020520 whitened brown adipose tissue morphology IAGP N RGD:5509061 20210225 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0031600 increased white adipose tissue apoptosis IAGP N RGD:5509061 20240229 MGI PMID:33027649 1620429 Med19 mediator complex subunit 19 gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240321 MGI PMID:33027649 1620430 Pjvk pejvakin gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:17329413 1620430 Pjvk pejvakin gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1620430 Pjvk pejvakin gene MP:0001410 head bobbing IEA N RGD:5509061 20210826 MGI 1620430 Pjvk pejvakin gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17329413 1620430 Pjvk pejvakin gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:17329413 1620430 Pjvk pejvakin gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210826 MGI 1620430 Pjvk pejvakin gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210826 MGI 1620430 Pjvk pejvakin gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:16804542 1620430 Pjvk pejvakin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16804542 1620430 Pjvk pejvakin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17329413 1620432 Prdm12 PR domain containing 12 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20200213 MGI PMID:30917309 1620432 Prdm12 PR domain containing 12 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20200213 MGI PMID:30917309 1620432 Prdm12 PR domain containing 12 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20200213 MGI PMID:30917309 1620432 Prdm12 PR domain containing 12 gene MP:0001097 abnormal superior glossopharyngeal ganglion morphology IAGP N RGD:5509061 20200213 MGI PMID:30917309 1620432 Prdm12 PR domain containing 12 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20160421 MGI 1620432 Prdm12 PR domain containing 12 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1620432 Prdm12 PR domain containing 12 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20170105 MGI 1620432 Prdm12 PR domain containing 12 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200213 MGI PMID:30917309 1620432 Prdm12 PR domain containing 12 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20170105 MGI 1620432 Prdm12 PR domain containing 12 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20200213 MGI PMID:30917309 1620432 Prdm12 PR domain containing 12 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20200213 MGI PMID:30917309 1620432 Prdm12 PR domain containing 12 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20211021 MGI 1620432 Prdm12 PR domain containing 12 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200213 MGI PMID:30917309 1620432 Prdm12 PR domain containing 12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 1620435 Spag6 sperm associated antigen 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20220324 MGI PMID:35159146 1620436 Tmem182 transmembrane protein 182 gene MP:0001260 increased body weight IAGP N RGD:5509061 20240620 MGI PMID:34427057 1620436 Tmem182 transmembrane protein 182 gene MP:0001264 increased body size IAGP N RGD:5509061 20240620 MGI PMID:34427057 1620436 Tmem182 transmembrane protein 182 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20240620 MGI PMID:34427057 1620436 Tmem182 transmembrane protein 182 gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20240620 MGI PMID:34427057 1620436 Tmem182 transmembrane protein 182 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20240620 MGI PMID:34427057 1620436 Tmem182 transmembrane protein 182 gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20240620 MGI PMID:34427057 1620436 Tmem182 transmembrane protein 182 gene MP:0009405 increased skeletal muscle fiber number IAGP N RGD:5509061 20240620 MGI PMID:34427057 1620436 Tmem182 transmembrane protein 182 gene MP:0009421 increased gastrocnemius weight IAGP N RGD:5509061 20240620 MGI PMID:34427057 1620436 Tmem182 transmembrane protein 182 gene MP:0009427 increased tibialis anterior weight IAGP N RGD:5509061 20240620 MGI PMID:34427057 1620436 Tmem182 transmembrane protein 182 gene MP:0010226 increased quadriceps weight IAGP N RGD:5509061 20240620 MGI PMID:34427057 1620436 Tmem182 transmembrane protein 182 gene MP:0010238 increased skeletal muscle weight IAGP N RGD:5509061 20240620 MGI PMID:34427057 1620436 Tmem182 transmembrane protein 182 gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20240620 MGI PMID:34427057 1620436 Tmem182 transmembrane protein 182 gene MP:0030945 abnormal myoblast migration IAGP N RGD:5509061 20240620 MGI PMID:34427057 1620436 Tmem182 transmembrane protein 182 gene MP:0030959 abnormal myoblast fusion IAGP N RGD:5509061 20240620 MGI PMID:34427057 1620436 Tmem182 transmembrane protein 182 gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20240620 MGI PMID:34427057 1620440 Nsl1 NSL1, MIS12 kinetochore complex component gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1620440 Nsl1 NSL1, MIS12 kinetochore complex component gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1620440 Nsl1 NSL1, MIS12 kinetochore complex component gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240919 MGI 1620440 Nsl1 NSL1, MIS12 kinetochore complex component gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1620440 Nsl1 NSL1, MIS12 kinetochore complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620440 Nsl1 NSL1, MIS12 kinetochore complex component gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20240919 MGI 1620440 Nsl1 NSL1, MIS12 kinetochore complex component gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 1620440 Nsl1 NSL1, MIS12 kinetochore complex component gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240926 MGI 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0001127 small ovary IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0001147 small testis IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0001924 infertility IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0001925 male infertility IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0001926 female infertility IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20141003 MGI 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20230601 MGI 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0004805 absent oocytes IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0005159 azoospermia IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20230601 MGI 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0013236 ovary degeneration IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620443 Firrm FIGNL1 interacting regulator of recombination and mitosis gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20240606 MGI PMID:37439366 1620444 Bpifb3 BPI fold containing family B, member 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1620445 Scgb1c1 secretoglobin, family 1C, member 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1620448 Nctc1 non-coding transcript 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 1620449 Btbd16 BTB domain containing 16 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1620449 Btbd16 BTB domain containing 16 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20190502 MGI 1620449 Btbd16 BTB domain containing 16 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20210128 MGI 1620449 Btbd16 BTB domain containing 16 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20220519 MGI 1620449 Btbd16 BTB domain containing 16 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1620456 Syt14 synaptotagmin XIV gene MP:0000745 tremors IEA N RGD:5509061 20240523 MGI 1620461 Fads6 fatty acid desaturase domain family, member 6 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 1620461 Fads6 fatty acid desaturase domain family, member 6 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210826 MGI 1620461 Fads6 fatty acid desaturase domain family, member 6 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20200514 MGI 1620461 Fads6 fatty acid desaturase domain family, member 6 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1620461 Fads6 fatty acid desaturase domain family, member 6 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1620461 Fads6 fatty acid desaturase domain family, member 6 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20210520 MGI 1620461 Fads6 fatty acid desaturase domain family, member 6 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 1620461 Fads6 fatty acid desaturase domain family, member 6 gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20210826 MGI 1620461 Fads6 fatty acid desaturase domain family, member 6 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210826 MGI 1620461 Fads6 fatty acid desaturase domain family, member 6 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210826 MGI 1620461 Fads6 fatty acid desaturase domain family, member 6 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210826 MGI 1620461 Fads6 fatty acid desaturase domain family, member 6 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210826 MGI 1620461 Fads6 fatty acid desaturase domain family, member 6 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20200514 MGI 1620466 Tafa1 TAFA chemokine like family member 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1620466 Tafa1 TAFA chemokine like family member 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20200402 MGI PMID:31689372 1620466 Tafa1 TAFA chemokine like family member 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1620466 Tafa1 TAFA chemokine like family member 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20200402 MGI PMID:31689372 1620466 Tafa1 TAFA chemokine like family member 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230601 MGI 1620466 Tafa1 TAFA chemokine like family member 1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20200402 MGI PMID:31689372 1620466 Tafa1 TAFA chemokine like family member 1 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20200402 MGI PMID:31689372 1620466 Tafa1 TAFA chemokine like family member 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1620466 Tafa1 TAFA chemokine like family member 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20200402 MGI PMID:31689372 1620466 Tafa1 TAFA chemokine like family member 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20200402 MGI PMID:31689372 1620466 Tafa1 TAFA chemokine like family member 1 gene MP:0011945 increased eating frequency IAGP N RGD:5509061 20200402 MGI PMID:31689372 1620466 Tafa1 TAFA chemokine like family member 1 gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20200402 MGI PMID:31689372 1620466 Tafa1 TAFA chemokine like family member 1 gene MP:0020422 decreased freezing behavior IAGP N RGD:5509061 20200402 MGI PMID:31689372 1620466 Tafa1 TAFA chemokine like family member 1 gene MP:0020874 abnormal nervous system dopamine level IAGP N RGD:5509061 20200402 MGI PMID:31689372 1620466 Tafa1 TAFA chemokine like family member 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:31689372 1620468 Dlec1 deleted in lung and esophageal cancer 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20210722 MGI PMID:33144677 1620468 Dlec1 deleted in lung and esophageal cancer 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20210722 MGI PMID:33144677 1620468 Dlec1 deleted in lung and esophageal cancer 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210722 MGI PMID:33144677 1620468 Dlec1 deleted in lung and esophageal cancer 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210722 MGI PMID:33144677 1620468 Dlec1 deleted in lung and esophageal cancer 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1620468 Dlec1 deleted in lung and esophageal cancer 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1620468 Dlec1 deleted in lung and esophageal cancer 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1620468 Dlec1 deleted in lung and esophageal cancer 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20210722 MGI PMID:33144677 1620468 Dlec1 deleted in lung and esophageal cancer 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20210722 MGI PMID:33144677 1620468 Dlec1 deleted in lung and esophageal cancer 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210722 MGI PMID:33144677 1620468 Dlec1 deleted in lung and esophageal cancer 1 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20210722 MGI PMID:33144677 1620468 Dlec1 deleted in lung and esophageal cancer 1 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20210722 MGI PMID:33144677 1620468 Dlec1 deleted in lung and esophageal cancer 1 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20210722 MGI PMID:33144677 1620469 Ttll5 tubulin tyrosine ligase-like family, member 5 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20200109 MGI PMID:27162334 1620469 Ttll5 tubulin tyrosine ligase-like family, member 5 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200109 MGI PMID:27162334 1620469 Ttll5 tubulin tyrosine ligase-like family, member 5 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23558686 1620469 Ttll5 tubulin tyrosine ligase-like family, member 5 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23558686 1620469 Ttll5 tubulin tyrosine ligase-like family, member 5 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23558686 1620469 Ttll5 tubulin tyrosine ligase-like family, member 5 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20200109 MGI PMID:27162334 1620469 Ttll5 tubulin tyrosine ligase-like family, member 5 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23558686 1620469 Ttll5 tubulin tyrosine ligase-like family, member 5 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23558686 1620469 Ttll5 tubulin tyrosine ligase-like family, member 5 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200109 MGI PMID:27162334 1620469 Ttll5 tubulin tyrosine ligase-like family, member 5 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:23558686 1620469 Ttll5 tubulin tyrosine ligase-like family, member 5 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:23558686 1620469 Ttll5 tubulin tyrosine ligase-like family, member 5 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20141003 MGI PMID:23558686 1620469 Ttll5 tubulin tyrosine ligase-like family, member 5 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200109 MGI PMID:27162334 1620469 Ttll5 tubulin tyrosine ligase-like family, member 5 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200109 MGI PMID:27162334 1620471 Ccdc66 coiled-coil domain containing 66 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21680557 1620471 Ccdc66 coiled-coil domain containing 66 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20240523 MGI 1620471 Ccdc66 coiled-coil domain containing 66 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21680557 1620471 Ccdc66 coiled-coil domain containing 66 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21680557 1620471 Ccdc66 coiled-coil domain containing 66 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21680557 1620471 Ccdc66 coiled-coil domain containing 66 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21680557 1620471 Ccdc66 coiled-coil domain containing 66 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21680557 1620471 Ccdc66 coiled-coil domain containing 66 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 1620471 Ccdc66 coiled-coil domain containing 66 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20240523 MGI 1620471 Ccdc66 coiled-coil domain containing 66 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21680557 1620471 Ccdc66 coiled-coil domain containing 66 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21680557 1620471 Ccdc66 coiled-coil domain containing 66 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21680557 1620471 Ccdc66 coiled-coil domain containing 66 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21680557 1620473 Ccdc171 coiled-coil domain containing 171 gene MP:0002491 decreased IgD level IEA N RGD:5509061 20200310 MGI 1620473 Ccdc171 coiled-coil domain containing 171 gene MP:0002494 increased IgM level IEA N RGD:5509061 20200310 MGI 1620473 Ccdc171 coiled-coil domain containing 171 gene MP:0008211 decreased mature B cell number IEA N RGD:5509061 20200310 MGI 1620477 Pik3r5 phosphoinositide-3-kinase regulatory subunit 5 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20170713 MGI PMID:25605974 1620477 Pik3r5 phosphoinositide-3-kinase regulatory subunit 5 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:17041586 1620477 Pik3r5 phosphoinositide-3-kinase regulatory subunit 5 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17041586 1620477 Pik3r5 phosphoinositide-3-kinase regulatory subunit 5 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20170713 MGI PMID:25605974 1620481 Tcfl5 transcription factor-like 5 (basic helix-loop-helix) gene MP:0001147 small testis IAGP N RGD:5509061 20220811 MGI PMID:35768632 1620481 Tcfl5 transcription factor-like 5 (basic helix-loop-helix) gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220811 MGI PMID:35768632 1620481 Tcfl5 transcription factor-like 5 (basic helix-loop-helix) gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220811 MGI PMID:35768632 1620481 Tcfl5 transcription factor-like 5 (basic helix-loop-helix) gene MP:0001925 male infertility IAGP N RGD:5509061 20220811 MGI PMID:35768632 1620481 Tcfl5 transcription factor-like 5 (basic helix-loop-helix) gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220811 MGI PMID:35768632 1620481 Tcfl5 transcription factor-like 5 (basic helix-loop-helix) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220811 MGI PMID:35768632 1620481 Tcfl5 transcription factor-like 5 (basic helix-loop-helix) gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220811 MGI PMID:35768632 1620481 Tcfl5 transcription factor-like 5 (basic helix-loop-helix) gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220811 MGI PMID:35768632 1620481 Tcfl5 transcription factor-like 5 (basic helix-loop-helix) gene MP:0005159 azoospermia IAGP N RGD:5509061 20220811 MGI PMID:35768632 1620481 Tcfl5 transcription factor-like 5 (basic helix-loop-helix) gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220811 MGI PMID:35768632 1620481 Tcfl5 transcription factor-like 5 (basic helix-loop-helix) gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20220811 MGI PMID:35768632 1620481 Tcfl5 transcription factor-like 5 (basic helix-loop-helix) gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20220811 MGI PMID:35768632 1620481 Tcfl5 transcription factor-like 5 (basic helix-loop-helix) gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220811 MGI PMID:35768632 1620481 Tcfl5 transcription factor-like 5 (basic helix-loop-helix) gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220811 MGI PMID:35768632 1620485 Tmem132e transmembrane protein 132E gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20240523 MGI 1620485 Tmem132e transmembrane protein 132E gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20240523 MGI 1620485 Tmem132e transmembrane protein 132E gene MP:0009455 enhanced cued conditioning behavior IEA N RGD:5509061 20230601 MGI 1620485 Tmem132e transmembrane protein 132E gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1620486 Kics2 KICSTOR subunit 2 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1620486 Kics2 KICSTOR subunit 2 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20230601 MGI 1620486 Kics2 KICSTOR subunit 2 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1620486 Kics2 KICSTOR subunit 2 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20230601 MGI 1620487 Clspn claspin gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0001935 decreased litter size IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0002981 increased liver weight IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0003718 maternal effect IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0005014 increased B cell number IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0005516 enhanced liver regeneration IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0008976 delayed female fertility IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:27401717 1620487 Clspn claspin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620487 Clspn claspin gene MP:0014443 impaired polar body extrusion IAGP N RGD:5509061 20240509 MGI PMID:36240068 1620487 Clspn claspin gene MP:0031269 increased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620487 Clspn claspin gene MP:0031271 increased susceptibility to age-related hepatic steatosis IAGP N RGD:5509061 20230119 MGI PMID:36240068 1620489 Rnf217 ring finger protein 217 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1620489 Rnf217 ring finger protein 217 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20240718 MGI PMID:33895792 1620489 Rnf217 ring finger protein 217 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20240718 MGI PMID:33895792 1620489 Rnf217 ring finger protein 217 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20240718 MGI PMID:33895792 1620490 Samd3 sterile alpha motif domain containing 3 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1620490 Samd3 sterile alpha motif domain containing 3 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20220428 MGI PMID:34626120 1620490 Samd3 sterile alpha motif domain containing 3 gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20220428 MGI PMID:34626120 1620490 Samd3 sterile alpha motif domain containing 3 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20220428 MGI PMID:34626120 1620490 Samd3 sterile alpha motif domain containing 3 gene MP:0010839 decreased CD8-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20220428 MGI PMID:34626120 1620491 Prss45 serine protease 45 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1620492 Mfrp membrane frizzled-related protein gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:21810984 1620492 Mfrp membrane frizzled-related protein gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:10967077 1620492 Mfrp membrane frizzled-related protein gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:21810984 1620492 Mfrp membrane frizzled-related protein gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:21810984 1620492 Mfrp membrane frizzled-related protein gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21810984 1620492 Mfrp membrane frizzled-related protein gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21810984 1620492 Mfrp membrane frizzled-related protein gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21810984 1620492 Mfrp membrane frizzled-related protein gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21810984 1620492 Mfrp membrane frizzled-related protein gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:10967077 1620492 Mfrp membrane frizzled-related protein gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21810984 1620492 Mfrp membrane frizzled-related protein gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21810984 1620492 Mfrp membrane frizzled-related protein gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:21810984 1620492 Mfrp membrane frizzled-related protein gene MP:0012029 abnormal electroretinogram waveform feature IEA N RGD:5509061 20240328 MGI 1620492 Mfrp membrane frizzled-related protein gene MP:0012143 decreased a-wave amplitude IEA N RGD:5509061 20240328 MGI 1620492 Mfrp membrane frizzled-related protein gene MP:0012144 decreased b-wave amplitude IEA N RGD:5509061 20240328 MGI 1620492 Mfrp membrane frizzled-related protein gene MP:0012671 retina spots IAGP N RGD:5509061 20141003 MGI PMID:10967077 1620548 Otoa otoancorin gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1620548 Otoa otoancorin gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:23129639 1620548 Otoa otoancorin gene MP:0003150 detached tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:23129639 1620548 Otoa otoancorin gene MP:0004415 abnormal cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:23129639 1620548 Otoa otoancorin gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1620548 Otoa otoancorin gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1620548 Otoa otoancorin gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:23129639 1620548 Otoa otoancorin gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1620548 Otoa otoancorin gene MP:0013962 absent Hensen stripe IAGP N RGD:5509061 20160310 MGI PMID:23129639 1620549 Vasn vasorin gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:21658601 1620549 Vasn vasorin gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:21658601 1620549 Vasn vasorin gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21658601 1620549 Vasn vasorin gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21658601 1620549 Vasn vasorin gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21658601 1620549 Vasn vasorin gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:21658601 1620549 Vasn vasorin gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:21658601 1620549 Vasn vasorin gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:21658601 1620549 Vasn vasorin gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21658601 1620550 Tmem266 transmembrane protein 266 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20220721 MGI PMID:35574701 1620551 Tnfaip8l3 tumor necrosis factor, alpha-induced protein 8-like 3 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20200310 MGI PMID:25242044 1620551 Tnfaip8l3 tumor necrosis factor, alpha-induced protein 8-like 3 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20200310 MGI PMID:25242044 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200402 MGI 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210128 MGI 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0002343 abnormal lymph node cortex morphology IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0002345 abnormal lymph node primary follicle morphology IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0002493 increased IgG level IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0002494 increased IgM level IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0002495 increased IgA level IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0005014 increased B cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0005015 increased T cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200402 MGI 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620552 Zc3h12c zinc finger CCCH type containing 12C gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 1620553 Layn layilin gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20210429 MGI PMID:32539073 1620553 Layn layilin gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20210429 MGI PMID:32539073 1620556 Grip2 glutamate receptor interacting protein 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:14730302 1620556 Grip2 glutamate receptor interacting protein 2 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:18509036 1620556 Grip2 glutamate receptor interacting protein 2 gene MP:0005242 cryptophthalmos IAGP N RGD:5509061 20141003 MGI PMID:14730302 1620557 BC048671 cDNA sequence BC048671 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240627 MGI PMID:38835510 1620558 H1f10 H1.10 linker histone gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20210826 MGI 1620558 H1f10 H1.10 linker histone gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1620558 H1f10 H1.10 linker histone gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20211021 MGI 1620558 H1f10 H1.10 linker histone gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210128 MGI 1620558 H1f10 H1.10 linker histone gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1620558 H1f10 H1.10 linker histone gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1620558 H1f10 H1.10 linker histone gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20200402 MGI 1620558 H1f10 H1.10 linker histone gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1620560 Fam110b family with sequence similarity 110, member B gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20160804 MGI 1620560 Fam110b family with sequence similarity 110, member B gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20160804 MGI 1620560 Fam110b family with sequence similarity 110, member B gene MP:0005316 abnormal response to tactile stimuli IEA N RGD:5509061 20160804 MGI 1620560 Fam110b family with sequence similarity 110, member B gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20160804 MGI 1620560 Fam110b family with sequence similarity 110, member B gene MP:0008211 decreased mature B cell number IEA N RGD:5509061 20160804 MGI 1620561 Sdr16c6 short chain dehydrogenase/reductase family 16C, member 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200402 MGI PMID:31562240 1620561 Sdr16c6 short chain dehydrogenase/reductase family 16C, member 6 gene MP:0006167 eyelid edema IAGP N RGD:5509061 20200402 MGI PMID:31562240 1620561 Sdr16c6 short chain dehydrogenase/reductase family 16C, member 6 gene MP:0009002 premature hair regrowth IAGP N RGD:5509061 20200402 MGI PMID:31562240 1620562 Sdr16c5 short chain dehydrogenase/reductase family 16C, member 5 gene MP:0006167 eyelid edema IAGP N RGD:5509061 20200402 MGI PMID:31562240 1620562 Sdr16c5 short chain dehydrogenase/reductase family 16C, member 5 gene MP:0009002 premature hair regrowth IAGP N RGD:5509061 20200402 MGI PMID:31562240 1620563 Slc44a5 solute carrier family 44, member 5 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1620564 Dnai3 dynein axonemal intermediate chain 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20191205 MGI PMID:26501274 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210826 MGI 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20151015 MGI PMID:24598786 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20151015 MGI PMID:24598786 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20151015 MGI PMID:24598786 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20170713 MGI PMID:26427409 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210826 MGI 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20151015 MGI PMID:24598786 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20151015 MGI PMID:24598786 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20151015 MGI PMID:24598786 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20170713 MGI PMID:26427409 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0012145 increased a-wave amplitude IAGP N RGD:5509061 20151015 MGI PMID:24598786 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0012147 increased a-wave implicit time IAGP N RGD:5509061 20151015 MGI PMID:24598786 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0012150 increased b-wave implicit time IAGP N RGD:5509061 20151015 MGI PMID:24598786 1620565 Lrit3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210520 MGI 1620569 Vsig8 V-set and immunoglobulin domain containing 8 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1620569 Vsig8 V-set and immunoglobulin domain containing 8 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1620569 Vsig8 V-set and immunoglobulin domain containing 8 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20220519 MGI 1620569 Vsig8 V-set and immunoglobulin domain containing 8 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20220519 MGI 1620569 Vsig8 V-set and immunoglobulin domain containing 8 gene MP:0010571 shortened ST segment IEA N RGD:5509061 20210128 MGI 1620570 AU021092 expressed sequence AU021092 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20231207 MGI 1620570 AU021092 expressed sequence AU021092 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1620570 AU021092 expressed sequence AU021092 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1620570 AU021092 expressed sequence AU021092 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20181227 MGI 1620570 AU021092 expressed sequence AU021092 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1620570 AU021092 expressed sequence AU021092 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1620570 AU021092 expressed sequence AU021092 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1620570 AU021092 expressed sequence AU021092 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1620571 Krt90 keratin 90 gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20150903 MGI 1620571 Krt90 keratin 90 gene MP:0000583 long toenails IEA N RGD:5509061 20150903 MGI 1620571 Krt90 keratin 90 gene MP:0001406 abnormal gait IEA N RGD:5509061 20240523 MGI 1620571 Krt90 keratin 90 gene MP:0010102 increased caudal vertebrae number IEA N RGD:5509061 20150903 MGI 1620571 Krt90 keratin 90 gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20150903 MGI 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620572 C1ql4 complement component 1, q subcomponent-like 4 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20240418 MGI PMID:35579659 1620573 Ccdc184 coiled-coil domain containing 184 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 1620576 Slc2a13 solute carrier family 2 (facilitated glucose transporter), member 13 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20190502 MGI 1620576 Slc2a13 solute carrier family 2 (facilitated glucose transporter), member 13 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1620579 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20160811 MGI 1620579 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22057188 1620579 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160421 MGI 1620579 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:22057188 1620579 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:23375655 1620579 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1620579 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20160421 MGI 1620579 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:22057188 1620579 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1620579 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene MP:0009562 abnormal odor adaptation IAGP N RGD:5509061 20141003 MGI PMID:22057188 1620579 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene MP:0010055 abnormal sensory neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22057188 1620579 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 1620579 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1620579 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1620579 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20180215 MGI PMID:23375655 1620581 Zdhhc22 zinc finger, DHHC-type containing 22 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220519 MGI 1620581 Zdhhc22 zinc finger, DHHC-type containing 22 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220519 MGI 1620582 Vash1 vasohibin 1 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19204325 1620583 Lhfpl1 lipoma HMGIC fusion partner-like 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20200310 MGI 1620584 Rbm41 RNA binding motif protein 41 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1620590 Cib3 calcium and integrin binding family member 3 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20201231 MGI 1620590 Cib3 calcium and integrin binding family member 3 gene MP:0001304 cataract IEA N RGD:5509061 20200402 MGI 1620590 Cib3 calcium and integrin binding family member 3 gene MP:0001394 circling IAGP N RGD:5509061 20240328 MGI PMID:37001993 1620590 Cib3 calcium and integrin binding family member 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1620590 Cib3 calcium and integrin binding family member 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1620590 Cib3 calcium and integrin binding family member 3 gene MP:0001512 trunk curl IEA N RGD:5509061 20200402 MGI 1620590 Cib3 calcium and integrin binding family member 3 gene MP:0001525 impaired balance IAGP N RGD:5509061 20240328 MGI PMID:37001993 1620590 Cib3 calcium and integrin binding family member 3 gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20201022 MGI 1620590 Cib3 calcium and integrin binding family member 3 gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20240328 MGI PMID:37001993 1620590 Cib3 calcium and integrin binding family member 3 gene MP:0004517 decreased vestibular hair cell stereocilia number IAGP N RGD:5509061 20240328 MGI PMID:37001993 1620590 Cib3 calcium and integrin binding family member 3 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20230601 MGI 1620591 Zfp961 zinc finger protein 961 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1620591 Zfp961 zinc finger protein 961 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1620591 Zfp961 zinc finger protein 961 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220811 MGI 1620591 Zfp961 zinc finger protein 961 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 1620595 Dpy19l3 dpy-19 like C-mannosyltransferase 3 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20200310 MGI 1620595 Dpy19l3 dpy-19 like C-mannosyltransferase 3 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20200310 MGI 1620595 Dpy19l3 dpy-19 like C-mannosyltransferase 3 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20200310 MGI 1620595 Dpy19l3 dpy-19 like C-mannosyltransferase 3 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20200310 MGI 1620599 Fbxl18 F-box and leucine-rich repeat protein 18 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201231 MGI 1620599 Fbxl18 F-box and leucine-rich repeat protein 18 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1620599 Fbxl18 F-box and leucine-rich repeat protein 18 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1620601 Pilra paired immunoglobin-like type 2 receptor alpha gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23142774 1620601 Pilra paired immunoglobin-like type 2 receptor alpha gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:23142774 1620601 Pilra paired immunoglobin-like type 2 receptor alpha gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23142774 1620601 Pilra paired immunoglobin-like type 2 receptor alpha gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:23142774 1620601 Pilra paired immunoglobin-like type 2 receptor alpha gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23142774 1620601 Pilra paired immunoglobin-like type 2 receptor alpha gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23142774 1620601 Pilra paired immunoglobin-like type 2 receptor alpha gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:23142774 1620601 Pilra paired immunoglobin-like type 2 receptor alpha gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23142774 1620601 Pilra paired immunoglobin-like type 2 receptor alpha gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23142774 1620601 Pilra paired immunoglobin-like type 2 receptor alpha gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210211 MGI PMID:23142774 1620601 Pilra paired immunoglobin-like type 2 receptor alpha gene MP:0012246 abnormal hepatic cord morphology IAGP N RGD:5509061 20141003 MGI PMID:23142774 1620602 Fam151a family with sequence simliarity 151, member A gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20200730 MGI PMID:31949211 1620602 Fam151a family with sequence simliarity 151, member A gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20200730 MGI PMID:31949211 1620602 Fam151a family with sequence simliarity 151, member A gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200730 MGI PMID:31949211 1620602 Fam151a family with sequence simliarity 151, member A gene MP:0020816 decreased photoreceptor outer segment number IAGP N RGD:5509061 20200730 MGI PMID:31949211 1620604 Efcab7 EF-hand calcium binding domain 7 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1620604 Efcab7 EF-hand calcium binding domain 7 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1620606 Ccdc148 coiled-coil domain containing 148 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20240523 MGI 1620607 Ifi205 interferon activated gene 205 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20240523 MGI 1620607 Ifi205 interferon activated gene 205 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20240523 MGI 1620607 Ifi205 interferon activated gene 205 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1620607 Ifi205 interferon activated gene 205 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20240523 MGI 1620607 Ifi205 interferon activated gene 205 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1620607 Ifi205 interferon activated gene 205 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1620609 Tstd1 thiosulfate sulfurtransferase (rhodanese)-like domain containing 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20230601 MGI 1620609 Tstd1 thiosulfate sulfurtransferase (rhodanese)-like domain containing 1 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20230601 MGI 1620610 Arhgap30 Rho GTPase activating protein 30 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210520 MGI 1620610 Arhgap30 Rho GTPase activating protein 30 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1620610 Arhgap30 Rho GTPase activating protein 30 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210520 MGI 1620610 Arhgap30 Rho GTPase activating protein 30 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 1620610 Arhgap30 Rho GTPase activating protein 30 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1620610 Arhgap30 Rho GTPase activating protein 30 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1620610 Arhgap30 Rho GTPase activating protein 30 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1620613 Gm4846 predicted gene 4846 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240627 MGI PMID:38835510 1620617 Atp13a3 ATPase type 13A3 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20221215 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20231207 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230601 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0001925 male infertility IEA N RGD:5509061 20220811 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20221215 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20221215 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20230601 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0002833 increased heart weight IEA N RGD:5509061 20221215 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20221215 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20221215 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20230601 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20221215 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230601 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20230601 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20230601 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20221215 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20221215 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20220811 MGI 1620617 Atp13a3 ATPase type 13A3 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20221215 MGI 1620619 Rtp2 receptor transporter protein 2 gene MP:0001924 infertility IEA N RGD:5509061 20111116 MGI 1620620 Cyp2ab1 cytochrome P450, family 2, subfamily ab, polypeptide 1 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1620620 Cyp2ab1 cytochrome P450, family 2, subfamily ab, polypeptide 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1620620 Cyp2ab1 cytochrome P450, family 2, subfamily ab, polypeptide 1 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20201022 MGI 1620622 Spidr scaffolding protein involved in DNA repair gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1620622 Spidr scaffolding protein involved in DNA repair gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1620622 Spidr scaffolding protein involved in DNA repair gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1620622 Spidr scaffolding protein involved in DNA repair gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1620622 Spidr scaffolding protein involved in DNA repair gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1620622 Spidr scaffolding protein involved in DNA repair gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1620622 Spidr scaffolding protein involved in DNA repair gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20220811 MGI 1620623 Sema3g sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3G gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:26319580 1620623 Sema3g sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3G gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:20947821 1620623 Sema3g sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3G gene MP:0004106 lymphatic vessel hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:26319580 1620623 Sema3g sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3G gene MP:0010197 abnormal lymphatic vessel endothelial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:26319580 1620624 Chdh choline dehydrogenase gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:20371614 1620624 Chdh choline dehydrogenase gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1620624 Chdh choline dehydrogenase gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1620624 Chdh choline dehydrogenase gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200102 MGI PMID:20371614 1620624 Chdh choline dehydrogenase gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1620624 Chdh choline dehydrogenase gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20200430 MGI PMID:31255657 1620624 Chdh choline dehydrogenase gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:20371614 1620624 Chdh choline dehydrogenase gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20141003 MGI PMID:20371614 1620624 Chdh choline dehydrogenase gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:20371614 1620624 Chdh choline dehydrogenase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20200430 MGI PMID:31255657 1620624 Chdh choline dehydrogenase gene MP:0021134 decreased amino acid betaine level IAGP N RGD:5509061 20220721 MGI PMID:31255657 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20181227 MGI 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20221215 MGI 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0001925 male infertility IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20160421 MGI 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0010052 increased grip strength IEA N RGD:5509061 20190502 MGI 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20160721 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:24244200 1620625 Baz1a bromodomain adjacent to zinc finger domain 1A gene MP:0031410 biflagellated sperm IAGP N RGD:5509061 20220630 MGI PMID:24244200 1620626 Slc44a3 solute carrier family 44, member 3 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 1620626 Slc44a3 solute carrier family 44, member 3 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20200310 MGI 1620626 Slc44a3 solute carrier family 44, member 3 gene MP:0001304 cataract IEA N RGD:5509061 20200310 MGI 1620626 Slc44a3 solute carrier family 44, member 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1620626 Slc44a3 solute carrier family 44, member 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 1620626 Slc44a3 solute carrier family 44, member 3 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1620626 Slc44a3 solute carrier family 44, member 3 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201231 MGI 1620626 Slc44a3 solute carrier family 44, member 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1620626 Slc44a3 solute carrier family 44, member 3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1620627 Frat2 frequently rearranged in advanced T cell lymphomas 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15681612 1620628 Ccdc110 coiled-coil domain containing 110 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20231207 MGI 1620628 Ccdc110 coiled-coil domain containing 110 gene MP:0000274 enlarged heart IEA N RGD:5509061 20231207 MGI 1620628 Ccdc110 coiled-coil domain containing 110 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20231207 MGI 1620628 Ccdc110 coiled-coil domain containing 110 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20231207 MGI 1620628 Ccdc110 coiled-coil domain containing 110 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20231207 MGI 1620629 Klhl32 kelch-like 32 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1620629 Klhl32 kelch-like 32 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20220519 MGI 1620629 Klhl32 kelch-like 32 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20220519 MGI 1620630 Mms22l MMS22-like, DNA repair protein gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20160804 MGI 1620630 Mms22l MMS22-like, DNA repair protein gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20160922 MGI PMID:24652767 1620630 Mms22l MMS22-like, DNA repair protein gene MP:0010770 preweaning lethality IAGP N RGD:5509061 20160922 MGI PMID:24652767 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20221215 MGI 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0001200 thick skin IEA N RGD:5509061 20210520 MGI 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0001575 cyanosis IAGP N RGD:5509061 20221110 MGI PMID:34794077 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20241017 MGI 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20241017 MGI 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20221110 MGI PMID:34794077 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20221110 MGI PMID:34794077 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0002582 disorganized extraembryonic tissue IEA N RGD:5509061 20241017 MGI 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20241017 MGI 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241017 MGI 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20221110 MGI PMID:34794077 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20221110 MGI PMID:34794077 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220519 MGI 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20221110 MGI PMID:34794077 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20221110 MGI PMID:34794077 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221110 MGI PMID:34794077 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20221110 MGI PMID:34794077 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1620633 Sepsecs Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1620635 Gpr139 G protein-coupled receptor 139 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200310 MGI 1620635 Gpr139 G protein-coupled receptor 139 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200310 MGI 1620635 Gpr139 G protein-coupled receptor 139 gene MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20201210 MGI PMID:31416932 1620635 Gpr139 G protein-coupled receptor 139 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20201210 MGI PMID:31416932 1620635 Gpr139 G protein-coupled receptor 139 gene MP:0009713 enhanced conditioned place preference behavior IAGP N RGD:5509061 20201210 MGI PMID:31416932 1620635 Gpr139 G protein-coupled receptor 139 gene MP:0009776 decreased behavioral withdrawal response IAGP N RGD:5509061 20201210 MGI PMID:31416932 1620635 Gpr139 G protein-coupled receptor 139 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1620637 Minar1 membrane integral NOTCH2 associated receptor 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20181227 MGI 1620638 Lcorl ligand dependent nuclear receptor corepressor-like gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 1620638 Lcorl ligand dependent nuclear receptor corepressor-like gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20220519 MGI 1620638 Lcorl ligand dependent nuclear receptor corepressor-like gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220519 MGI 1620638 Lcorl ligand dependent nuclear receptor corepressor-like gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220519 MGI 1620638 Lcorl ligand dependent nuclear receptor corepressor-like gene MP:0005655 increased aggression IEA N RGD:5509061 20221215 MGI 1620638 Lcorl ligand dependent nuclear receptor corepressor-like gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220519 MGI 1620638 Lcorl ligand dependent nuclear receptor corepressor-like gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1620639 Dip2c disco interacting protein 2 homolog C gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210128 MGI 1620639 Dip2c disco interacting protein 2 homolog C gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210826 MGI 1620639 Dip2c disco interacting protein 2 homolog C gene MP:0000642 enlarged adrenal glands IEA N RGD:5509061 20210128 MGI 1620639 Dip2c disco interacting protein 2 homolog C gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1620639 Dip2c disco interacting protein 2 homolog C gene MP:0000706 small thymus IEA N RGD:5509061 20210128 MGI 1620639 Dip2c disco interacting protein 2 homolog C gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210128 MGI 1620639 Dip2c disco interacting protein 2 homolog C gene MP:0001926 female infertility IAGP N RGD:5509061 20231130 MGI PMID:32707302 1620639 Dip2c disco interacting protein 2 homolog C gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201022 MGI 1620639 Dip2c disco interacting protein 2 homolog C gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20231130 MGI PMID:32707302 1620639 Dip2c disco interacting protein 2 homolog C gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210128 MGI 1620640 Shroom4 shroom family member 4 gene MP:0001314 cornea opacity IEA N RGD:5509061 20170105 MGI 1620641 Iqcj IQ motif containing J gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 1620641 Iqcj IQ motif containing J gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20201022 MGI 1620643 Utp14b UTP14B small subunit processome component gene MP:0001055 failure of neuromuscular synapse postsynaptic differentiation IAGP N RGD:5509061 20141003 MGI PMID:3401545 1620643 Utp14b UTP14B small subunit processome component gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:1346141 1620643 Utp14b UTP14B small subunit processome component gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:3401545 1620643 Utp14b UTP14B small subunit processome component gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:3401545 1620643 Utp14b UTP14B small subunit processome component gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15289605 1620643 Utp14b UTP14B small subunit processome component gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:3401545 1620643 Utp14b UTP14B small subunit processome component gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15289605 1620643 Utp14b UTP14B small subunit processome component gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:3401545 1620643 Utp14b UTP14B small subunit processome component gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:15289605 1620644 Mtmr11 myotubularin related protein 11 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20230119 MGI 1620644 Mtmr11 myotubularin related protein 11 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1620644 Mtmr11 myotubularin related protein 11 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1620644 Mtmr11 myotubularin related protein 11 gene MP:0001200 thick skin IEA N RGD:5509061 20230119 MGI 1620644 Mtmr11 myotubularin related protein 11 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230119 MGI 1620647 Acot8 acyl-CoA thioesterase 8 gene MP:0001257 increased body length IEA N RGD:5509061 20230601 MGI 1620648 Hdac10 histone deacetylase 10 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1620650 Rfxap regulatory factor X-associated protein gene MP:0001314 cornea opacity IEA N RGD:5509061 20240523 MGI 1620650 Rfxap regulatory factor X-associated protein gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1620650 Rfxap regulatory factor X-associated protein gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1620650 Rfxap regulatory factor X-associated protein gene MP:0005287 narrow eye opening IEA N RGD:5509061 20240523 MGI 1620650 Rfxap regulatory factor X-associated protein gene MP:0005542 cornea vascularization IEA N RGD:5509061 20240523 MGI 1620650 Rfxap regulatory factor X-associated protein gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20240523 MGI 1620650 Rfxap regulatory factor X-associated protein gene MP:0012121 sclerocornea IEA N RGD:5509061 20240523 MGI 1620652 Rac3 Rac family small GTPase 3 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:15964829 1620652 Rac3 Rac family small GTPase 3 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:15964829 1620652 Rac3 Rac family small GTPase 3 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:15964830 1620652 Rac3 Rac family small GTPase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15964830 1620652 Rac3 Rac family small GTPase 3 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20210701 MGI PMID:33879799 1620652 Rac3 Rac family small GTPase 3 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:15964829 1620652 Rac3 Rac family small GTPase 3 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20210701 MGI PMID:33879799 1620652 Rac3 Rac family small GTPase 3 gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20210701 MGI PMID:33879799 1620652 Rac3 Rac family small GTPase 3 gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20210701 MGI PMID:33879799 1620654 Tlr8 toll-like receptor 8 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0002870 decreased anti-insulin autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0008170 decreased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0008206 increased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20811154 1620654 Tlr8 toll-like receptor 8 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:20811154 1620655 Sertad3 SERTA domain containing 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1620655 Sertad3 SERTA domain containing 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210826 MGI 1620655 Sertad3 SERTA domain containing 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1620655 Sertad3 SERTA domain containing 3 gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20210211 MGI PMID:33147462 1620656 Rtn4ip1 reticulon 4 interacting protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620657 Nxf7 nuclear RNA export factor 7 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20150903 MGI PMID:23675524 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0001193 psoriasis IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0001193 psoriasis IAGP N RGD:5509061 20200723 MGI PMID:29980436 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0001195 flaky skin IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0001212 skin lesions IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0001214 skin hyperplasia IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20200723 MGI PMID:29980436 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0001874 acanthosis IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0001874 acanthosis IAGP N RGD:5509061 20200723 MGI PMID:29980436 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20200730 MGI PMID:29980436 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0003853 dry skin IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20200723 MGI PMID:29980436 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0008345 abnormal gamma-delta T cell number IAGP N RGD:5509061 20200723 MGI PMID:29980436 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200723 MGI PMID:29980436 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20190627 MGI PMID:29689250 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200723 MGI PMID:29980436 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0012573 decreased susceptibility to chemically induced skin inflammation IAGP N RGD:5509061 20191114 MGI PMID:29150564 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0012573 decreased susceptibility to chemically induced skin inflammation IAGP N RGD:5509061 20200723 MGI PMID:29980436 1620658 Card14 caspase recruitment domain family, member 14 gene MP:0012764 increased alpha-beta T cell number IAGP N RGD:5509061 20200723 MGI PMID:29980436 1620659 Otud7a OTU domain containing 7A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180503 MGI PMID:29395075 1620659 Otud7a OTU domain containing 7A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180503 MGI PMID:29395075 1620659 Otud7a OTU domain containing 7A gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20180503 MGI PMID:29395075 1620659 Otud7a OTU domain containing 7A gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20180503 MGI PMID:29395075 1620659 Otud7a OTU domain containing 7A gene MP:0003053 delayed tooth eruption IAGP N RGD:5509061 20180503 MGI PMID:29395075 1620659 Otud7a OTU domain containing 7A gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20180503 MGI PMID:29395075 1620659 Otud7a OTU domain containing 7A gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20180503 MGI PMID:29395075 1620659 Otud7a OTU domain containing 7A gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20180503 MGI PMID:29395075 1620659 Otud7a OTU domain containing 7A gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20180503 MGI PMID:29395075 1620659 Otud7a OTU domain containing 7A gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1620659 Otud7a OTU domain containing 7A gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20180503 MGI PMID:29395075 1620659 Otud7a OTU domain containing 7A gene MP:0021165 behavioral developmental delay IAGP N RGD:5509061 20220922 MGI PMID:29395075 1620663 Psg25 pregnancy-specific beta-1-glycoprotein 25 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20211021 MGI 1620663 Psg25 pregnancy-specific beta-1-glycoprotein 25 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1620663 Psg25 pregnancy-specific beta-1-glycoprotein 25 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1620664 Mbd6 methyl-CpG binding domain protein 6 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1620664 Mbd6 methyl-CpG binding domain protein 6 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1620664 Mbd6 methyl-CpG binding domain protein 6 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1620664 Mbd6 methyl-CpG binding domain protein 6 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1620664 Mbd6 methyl-CpG binding domain protein 6 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1620664 Mbd6 methyl-CpG binding domain protein 6 gene MP:0001258 decreased body length IEA N RGD:5509061 20210520 MGI 1620664 Mbd6 methyl-CpG binding domain protein 6 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1620664 Mbd6 methyl-CpG binding domain protein 6 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1620664 Mbd6 methyl-CpG binding domain protein 6 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1620664 Mbd6 methyl-CpG binding domain protein 6 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1620664 Mbd6 methyl-CpG binding domain protein 6 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 1620664 Mbd6 methyl-CpG binding domain protein 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620664 Mbd6 methyl-CpG binding domain protein 6 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1620665 M1ap meiosis 1 associated protein gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23269666 1620665 M1ap meiosis 1 associated protein gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:23269666 1620665 M1ap meiosis 1 associated protein gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:23269666 1620665 M1ap meiosis 1 associated protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23269666 1620665 M1ap meiosis 1 associated protein gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23269666 1620665 M1ap meiosis 1 associated protein gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23269666 1620665 M1ap meiosis 1 associated protein gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23269666 1620665 M1ap meiosis 1 associated protein gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23269666 1620665 M1ap meiosis 1 associated protein gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23269666 1620665 M1ap meiosis 1 associated protein gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23269666 1620665 M1ap meiosis 1 associated protein gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23269666 1620665 M1ap meiosis 1 associated protein gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23269666 1620665 M1ap meiosis 1 associated protein gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:23269666 1620665 M1ap meiosis 1 associated protein gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23269666 1620668 Hyal3 hyaluronoglucosaminidase 3 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20160421 MGI 1620668 Hyal3 hyaluronoglucosaminidase 3 gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20180125 MGI PMID:18762256 1620668 Hyal3 hyaluronoglucosaminidase 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1620668 Hyal3 hyaluronoglucosaminidase 3 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20180125 MGI PMID:18762256 1620668 Hyal3 hyaluronoglucosaminidase 3 gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20180125 MGI PMID:18762256 1620669 Ank2 ankyrin 2, brain gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:9832558 1620669 Ank2 ankyrin 2, brain gene MP:0001260 increased body weight IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9832558 1620669 Ank2 ankyrin 2, brain gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:9832558 1620669 Ank2 ankyrin 2, brain gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20211118 MGI PMID:31285321 1620669 Ank2 ankyrin 2, brain gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20211118 MGI PMID:31285321 1620669 Ank2 ankyrin 2, brain gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:9832558 1620669 Ank2 ankyrin 2, brain gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20230817 MGI PMID:37182735 1620669 Ank2 ankyrin 2, brain gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0002083 premature death IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20211118 MGI PMID:31285321 1620669 Ank2 ankyrin 2, brain gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20211118 MGI PMID:31285321 1620669 Ank2 ankyrin 2, brain gene MP:0002579 disorganized secondary lens fibers IAGP N RGD:5509061 20141003 MGI PMID:11449000 1620669 Ank2 ankyrin 2, brain gene MP:0002579 disorganized secondary lens fibers IAGP N RGD:5509061 20141003 MGI PMID:9832558 1620669 Ank2 ankyrin 2, brain gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20211118 MGI PMID:31285321 1620669 Ank2 ankyrin 2, brain gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20230817 MGI PMID:37182735 1620669 Ank2 ankyrin 2, brain gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20230817 MGI PMID:37182735 1620669 Ank2 ankyrin 2, brain gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0003928 increased heart rate variability IAGP N RGD:5509061 20141003 MGI PMID:20525877 1620669 Ank2 ankyrin 2, brain gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20230817 MGI PMID:37182735 1620669 Ank2 ankyrin 2, brain gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20230817 MGI PMID:37182735 1620669 Ank2 ankyrin 2, brain gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20211118 MGI PMID:31285321 1620669 Ank2 ankyrin 2, brain gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20230817 MGI PMID:37182735 1620669 Ank2 ankyrin 2, brain gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0005331 insulin resistance IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20230817 MGI PMID:37182735 1620669 Ank2 ankyrin 2, brain gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:9832558 1620669 Ank2 ankyrin 2, brain gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20211118 MGI PMID:31285321 1620669 Ank2 ankyrin 2, brain gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:20525877 1620669 Ank2 ankyrin 2, brain gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20141003 MGI PMID:9832558 1620669 Ank2 ankyrin 2, brain gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:9832558 1620669 Ank2 ankyrin 2, brain gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20525877 1620669 Ank2 ankyrin 2, brain gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0009682 abnormal anterior corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:9832558 1620669 Ank2 ankyrin 2, brain gene MP:0009683 abnormal lateral corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:9832558 1620669 Ank2 ankyrin 2, brain gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20230817 MGI PMID:37182735 1620669 Ank2 ankyrin 2, brain gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20230817 MGI PMID:37182735 1620669 Ank2 ankyrin 2, brain gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9832558 1620669 Ank2 ankyrin 2, brain gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9832558 1620669 Ank2 ankyrin 2, brain gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20150827 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20230817 MGI PMID:37182735 1620669 Ank2 ankyrin 2, brain gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20211118 MGI PMID:31285321 1620669 Ank2 ankyrin 2, brain gene MP:0012462 decreased brain internal capsule size IAGP N RGD:5509061 20141003 MGI PMID:9832558 1620669 Ank2 ankyrin 2, brain gene MP:0014373 increased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:31285321 1620669 Ank2 ankyrin 2, brain gene MP:0014375 increased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:31285321 1620669 Ank2 ankyrin 2, brain gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20211118 MGI PMID:31285321 1620669 Ank2 ankyrin 2, brain gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20211118 MGI PMID:31285321 1620669 Ank2 ankyrin 2, brain gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0031269 increased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:26168218 1620669 Ank2 ankyrin 2, brain gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:26168218 1620670 Hoxc11 homeobox C11 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:12050119 1620670 Hoxc11 homeobox C11 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12050119 1620670 Hoxc11 homeobox C11 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18942146 1620670 Hoxc11 homeobox C11 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12050119 1620670 Hoxc11 homeobox C11 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18942146 1620670 Hoxc11 homeobox C11 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12050119 1620670 Hoxc11 homeobox C11 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1620670 Hoxc11 homeobox C11 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12050119 1620670 Hoxc11 homeobox C11 gene MP:0003600 ectopic kidney IAGP N RGD:5509061 20141003 MGI PMID:12050119 1620670 Hoxc11 homeobox C11 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:12050119 1620670 Hoxc11 homeobox C11 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1620670 Hoxc11 homeobox C11 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1620670 Hoxc11 homeobox C11 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12869760 1620670 Hoxc11 homeobox C11 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12869760 1620670 Hoxc11 homeobox C11 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 1620670 Hoxc11 homeobox C11 gene MP:0004656 absent sacral vertebrae IAGP N RGD:5509061 20141003 MGI PMID:12869760 1620670 Hoxc11 homeobox C11 gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:12050119 1620670 Hoxc11 homeobox C11 gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:12050119 1620670 Hoxc11 homeobox C11 gene MP:0011366 absent metanephros IAGP N RGD:5509061 20141003 MGI PMID:12050119 1620670 Hoxc11 homeobox C11 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12050119 1620671 Txlna taxilin alpha gene MP:0001147 small testis IEA N RGD:5509061 20200402 MGI 1620671 Txlna taxilin alpha gene MP:0001406 abnormal gait IEA N RGD:5509061 20210128 MGI 1620671 Txlna taxilin alpha gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1620671 Txlna taxilin alpha gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1620671 Txlna taxilin alpha gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20220811 MGI 1620671 Txlna taxilin alpha gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20211021 MGI 1620671 Txlna taxilin alpha gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1620671 Txlna taxilin alpha gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20181227 MGI 1620673 Dsp desmoplakin gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0000274 enlarged heart IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0000416 sparse hair IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0000420 ruffled hair IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1620673 Dsp desmoplakin gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11239416 1620673 Dsp desmoplakin gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11781569 1620673 Dsp desmoplakin gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:11781569 1620673 Dsp desmoplakin gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20141003 MGI PMID:11781569 1620673 Dsp desmoplakin gene MP:0001511 disheveled coat IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:9864371 1620673 Dsp desmoplakin gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:9864371 1620673 Dsp desmoplakin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9864371 1620673 Dsp desmoplakin gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20201022 MGI 1620673 Dsp desmoplakin gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20220519 MGI 1620673 Dsp desmoplakin gene MP:0001874 acanthosis IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0002083 premature death IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9864371 1620673 Dsp desmoplakin gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210826 MGI 1620673 Dsp desmoplakin gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1620673 Dsp desmoplakin gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20151112 MGI PMID:25496840 1620673 Dsp desmoplakin gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20151112 MGI PMID:25496840 1620673 Dsp desmoplakin gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20201022 MGI 1620673 Dsp desmoplakin gene MP:0002946 delayed axon extension IAGP N RGD:5509061 20151112 MGI PMID:25496840 1620673 Dsp desmoplakin gene MP:0002952 ventricular cardiomyopathy IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:9864371 1620673 Dsp desmoplakin gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:11239416 1620673 Dsp desmoplakin gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20210826 MGI 1620673 Dsp desmoplakin gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0003812 abnormal hair medulla IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20230601 MGI 1620673 Dsp desmoplakin gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20230504 MGI PMID:36231013 1620673 Dsp desmoplakin gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0008767 abnormal hair medullary septa cells IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20151112 MGI PMID:25496840 1620673 Dsp desmoplakin gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20141003 MGI PMID:11781569 1620673 Dsp desmoplakin gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0010505 abnormal T wave IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0010546 abnormal subendocardium layer morphology IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0010636 bundle branch block IAGP N RGD:5509061 20150910 MGI PMID:24108106 1620673 Dsp desmoplakin gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9864371 1620673 Dsp desmoplakin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20230504 MGI PMID:36231013 1620673 Dsp desmoplakin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620673 Dsp desmoplakin gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0011919 abnormal R wave IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0012515 abnormal heart apex morphology IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1620673 Dsp desmoplakin gene MP:0030520 oral mucosa blisters IAGP N RGD:5509061 20190815 MGI PMID:25659760 1620673 Dsp desmoplakin gene MP:0031330 delayed peripheral nervous system regeneration IAGP N RGD:5509061 20220106 MGI PMID:25496840 1620675 Ccdc117 coiled-coil domain containing 117 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 1620675 Ccdc117 coiled-coil domain containing 117 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1620675 Ccdc117 coiled-coil domain containing 117 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1620675 Ccdc117 coiled-coil domain containing 117 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1620676 Rexo2 RNA exonuclease 2 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20201022 MGI 1620676 Rexo2 RNA exonuclease 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20210513 MGI PMID:31588022 1620676 Rexo2 RNA exonuclease 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20200310 MGI 1620676 Rexo2 RNA exonuclease 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20210513 MGI PMID:31588022 1620676 Rexo2 RNA exonuclease 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20220203 MGI PMID:31588022 1620676 Rexo2 RNA exonuclease 2 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1620676 Rexo2 RNA exonuclease 2 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 1620676 Rexo2 RNA exonuclease 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20200310 MGI 1620676 Rexo2 RNA exonuclease 2 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20210513 MGI PMID:31588022 1620676 Rexo2 RNA exonuclease 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620676 Rexo2 RNA exonuclease 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20200310 MGI 1620678 Apof apolipoprotein F gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20230601 MGI 1620678 Apof apolipoprotein F gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22363685 1620678 Apof apolipoprotein F gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20231207 MGI 1620678 Apof apolipoprotein F gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22363685 1620678 Apof apolipoprotein F gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20141003 MGI PMID:22363685 1620678 Apof apolipoprotein F gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22363685 1620678 Apof apolipoprotein F gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22363685 1620679 Rdh9 retinol dehydrogenase 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17270348 1620680 Igflr1 IGF-like family receptor 1 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1620680 Igflr1 IGF-like family receptor 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1620686 Oas1d 2'-5' oligoadenylate synthetase 1D gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15899864 1620686 Oas1d 2'-5' oligoadenylate synthetase 1D gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15899864 1620686 Oas1d 2'-5' oligoadenylate synthetase 1D gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15899864 1620686 Oas1d 2'-5' oligoadenylate synthetase 1D gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:15899864 1620686 Oas1d 2'-5' oligoadenylate synthetase 1D gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:15899864 1620686 Oas1d 2'-5' oligoadenylate synthetase 1D gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:15899864 1620688 Deptor DEP domain containing MTOR-interacting protein gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20190704 MGI PMID:28462079 1620688 Deptor DEP domain containing MTOR-interacting protein gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20240829 MGI PMID:36548081 1620688 Deptor DEP domain containing MTOR-interacting protein gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20190704 MGI PMID:28462079 1620688 Deptor DEP domain containing MTOR-interacting protein gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20190704 MGI PMID:28462079 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0008902 abnormal renal fat pad morphology IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0011310 abnormal kidney capillary morphology IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0011352 proximal convoluted tubule brush border loss IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0013284 abnormal renal glomerular filtration IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620691 Clec2h C-type lectin domain family 2, member h gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20220505 MGI PMID:35318366 1620694 Tmem121b transmembrane protein 121B gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20220519 MGI 1620694 Tmem121b transmembrane protein 121B gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1620694 Tmem121b transmembrane protein 121B gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1620694 Tmem121b transmembrane protein 121B gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20220519 MGI 1620696 Pde4dip phosphodiesterase 4D interacting protein (myomegalin) gene MP:0001399 hyperactivity IAGP N RGD:5509061 20150212 MGI PMID:25308000 1620696 Pde4dip phosphodiesterase 4D interacting protein (myomegalin) gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20150212 MGI PMID:25308000 1620696 Pde4dip phosphodiesterase 4D interacting protein (myomegalin) gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210520 MGI 1620696 Pde4dip phosphodiesterase 4D interacting protein (myomegalin) gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20201022 MGI 1620696 Pde4dip phosphodiesterase 4D interacting protein (myomegalin) gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 1620696 Pde4dip phosphodiesterase 4D interacting protein (myomegalin) gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20150212 MGI PMID:25308000 1620696 Pde4dip phosphodiesterase 4D interacting protein (myomegalin) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620696 Pde4dip phosphodiesterase 4D interacting protein (myomegalin) gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20211021 MGI 1620696 Pde4dip phosphodiesterase 4D interacting protein (myomegalin) gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20221215 MGI 1620696 Pde4dip phosphodiesterase 4D interacting protein (myomegalin) gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20221215 MGI 1620709 Skap1 src family associated phosphoprotein 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17646386 1620709 Skap1 src family associated phosphoprotein 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17646386 1620709 Skap1 src family associated phosphoprotein 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17646386 1620709 Skap1 src family associated phosphoprotein 1 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17646386 1620709 Skap1 src family associated phosphoprotein 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17646386 1620709 Skap1 src family associated phosphoprotein 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17646386 1620710 Tmem247 transmembrane protein 247 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1620717 1700034E13Rik RIKEN cDNA 1700034E13 gene gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210128 MGI 1620717 1700034E13Rik RIKEN cDNA 1700034E13 gene gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1620717 1700034E13Rik RIKEN cDNA 1700034E13 gene gene MP:0000599 enlarged liver IEA N RGD:5509061 20210128 MGI 1620717 1700034E13Rik RIKEN cDNA 1700034E13 gene gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1620717 1700034E13Rik RIKEN cDNA 1700034E13 gene gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1620717 1700034E13Rik RIKEN cDNA 1700034E13 gene gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1620717 1700034E13Rik RIKEN cDNA 1700034E13 gene gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 1620717 1700034E13Rik RIKEN cDNA 1700034E13 gene gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 1620717 1700034E13Rik RIKEN cDNA 1700034E13 gene gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1620717 1700034E13Rik RIKEN cDNA 1700034E13 gene gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1620717 1700034E13Rik RIKEN cDNA 1700034E13 gene gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1620717 1700034E13Rik RIKEN cDNA 1700034E13 gene gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1620717 1700034E13Rik RIKEN cDNA 1700034E13 gene gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1620717 1700034E13Rik RIKEN cDNA 1700034E13 gene gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210128 MGI 1620718 Cyren cell cycle regulator of NHEJ gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1620718 Cyren cell cycle regulator of NHEJ gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1620718 Cyren cell cycle regulator of NHEJ gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1620718 Cyren cell cycle regulator of NHEJ gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1620718 Cyren cell cycle regulator of NHEJ gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200402 MGI PMID:30017584 1620718 Cyren cell cycle regulator of NHEJ gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200402 MGI PMID:30017584 1620718 Cyren cell cycle regulator of NHEJ gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20200402 MGI PMID:30017584 1620718 Cyren cell cycle regulator of NHEJ gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20200402 MGI PMID:30017584 1620718 Cyren cell cycle regulator of NHEJ gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20210722 MGI PMID:31795137 1620718 Cyren cell cycle regulator of NHEJ gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200402 MGI PMID:30017584 1620718 Cyren cell cycle regulator of NHEJ gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20210722 MGI PMID:31795137 1620723 Tmem181a transmembrane protein 181A gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1620726 4930568D16Rik RIKEN cDNA 4930568D16 gene gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210708 MGI PMID:32561905 1620729 Pramex1 PRAME like, X-linked 1 gene MP:0001147 small testis IAGP N RGD:5509061 20201015 MGI PMID:32017313 1620729 Pramex1 PRAME like, X-linked 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20201015 MGI PMID:32017313 1620729 Pramex1 PRAME like, X-linked 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20201015 MGI PMID:32017313 1620729 Pramex1 PRAME like, X-linked 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20201015 MGI PMID:32017313 1620729 Pramex1 PRAME like, X-linked 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20201015 MGI PMID:32017313 1620729 Pramex1 PRAME like, X-linked 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20201015 MGI PMID:32017313 1620729 Pramex1 PRAME like, X-linked 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20201015 MGI PMID:32017313 1620729 Pramex1 PRAME like, X-linked 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20201015 MGI PMID:32017313 1620729 Pramex1 PRAME like, X-linked 1 gene MP:0006428 ectopic Sertoli cells IAGP N RGD:5509061 20201015 MGI PMID:32017313 1620729 Pramex1 PRAME like, X-linked 1 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20201015 MGI PMID:32017313 1620729 Pramex1 PRAME like, X-linked 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20201015 MGI PMID:32017313 1620730 Hormad2 HORMA domain containing 2 gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20240523 MGI 1620730 Hormad2 HORMA domain containing 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1620730 Hormad2 HORMA domain containing 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 1620730 Hormad2 HORMA domain containing 2 gene MP:0000692 small spleen IEA N RGD:5509061 20240523 MGI 1620730 Hormad2 HORMA domain containing 2 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 1620730 Hormad2 HORMA domain containing 2 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 1620730 Hormad2 HORMA domain containing 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:23039116 1620730 Hormad2 HORMA domain containing 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23039116 1620730 Hormad2 HORMA domain containing 2 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22549958 1620730 Hormad2 HORMA domain containing 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1620730 Hormad2 HORMA domain containing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22549958 1620730 Hormad2 HORMA domain containing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23039116 1620730 Hormad2 HORMA domain containing 2 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:22549958 1620730 Hormad2 HORMA domain containing 2 gene MP:0002311 abnormal inspiratory capacity IEA N RGD:5509061 20240627 MGI 1620730 Hormad2 HORMA domain containing 2 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:22549958 1620730 Hormad2 HORMA domain containing 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23039116 1620730 Hormad2 HORMA domain containing 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:23039116 1620730 Hormad2 HORMA domain containing 2 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:22549958 1620730 Hormad2 HORMA domain containing 2 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:23039116 1620730 Hormad2 HORMA domain containing 2 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:22549958 1620730 Hormad2 HORMA domain containing 2 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23039116 1620730 Hormad2 HORMA domain containing 2 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:23039116 1620730 Hormad2 HORMA domain containing 2 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22549958 1620730 Hormad2 HORMA domain containing 2 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23039116 1620730 Hormad2 HORMA domain containing 2 gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20141003 MGI PMID:22549958 1620730 Hormad2 HORMA domain containing 2 gene MP:0011045 decreased lung elastance IEA N RGD:5509061 20240523 MGI 1620730 Hormad2 HORMA domain containing 2 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20240523 MGI 1620731 Wdr64 WD repeat domain 64 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220811 MGI 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0001147 small testis IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0001925 male infertility IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0001926 female infertility IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220811 MGI 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0004805 absent oocytes IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0005159 azoospermia IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220519 MGI 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620733 4930447C04Rik RIKEN cDNA 4930447C04 gene gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20170608 MGI PMID:27796301 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001196 shiny skin IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001198 tight skin IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001201 translucent skin IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001230 epidermal desquamation IAGP N RGD:5509061 20141003 MGI PMID:18957418 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001238 thin epidermis stratum spinosum IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001238 thin epidermis stratum spinosum IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:18957418 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001429 dehydration IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001435 absent suckling reflex IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18957418 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0002177 abnormal outer ear morphology IEA N RGD:5509061 20201022 MGI 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:18957418 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:18957418 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20201022 MGI 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0003773 eclabion IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0003853 dry skin IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0009597 impaired stratum corneum desquamation IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0009599 thick epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0009599 thick epidermis stratum granulosum IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20141003 MGI PMID:18957418 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0009931 abnormal skin appearance IEA N RGD:5509061 20201022 MGI 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0010814 absent alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18632686 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18802465 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18957418 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180726 MGI PMID:27551807 1620735 Abca12 ATP-binding cassette, sub-family A member 12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1620736 Sppl3 signal peptide peptidase 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:20562862 1620736 Sppl3 signal peptide peptidase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20562862 1620736 Sppl3 signal peptide peptidase 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20221215 MGI 1620736 Sppl3 signal peptide peptidase 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20562862 1620736 Sppl3 signal peptide peptidase 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1620736 Sppl3 signal peptide peptidase 3 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:20562862 1620736 Sppl3 signal peptide peptidase 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1620736 Sppl3 signal peptide peptidase 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20562862 1620736 Sppl3 signal peptide peptidase 3 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:20562862 1620736 Sppl3 signal peptide peptidase 3 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:20562862 1620736 Sppl3 signal peptide peptidase 3 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20221215 MGI 1620736 Sppl3 signal peptide peptidase 3 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20221215 MGI 1620736 Sppl3 signal peptide peptidase 3 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:20562862 1620736 Sppl3 signal peptide peptidase 3 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20210422 MGI PMID:26851218 1620736 Sppl3 signal peptide peptidase 3 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20210422 MGI PMID:26851218 1620736 Sppl3 signal peptide peptidase 3 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20210422 MGI PMID:26851218 1620736 Sppl3 signal peptide peptidase 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20210422 MGI PMID:26851218 1620736 Sppl3 signal peptide peptidase 3 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220811 MGI 1620736 Sppl3 signal peptide peptidase 3 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20210422 MGI PMID:26851218 1620736 Sppl3 signal peptide peptidase 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210422 MGI PMID:26851218 1620736 Sppl3 signal peptide peptidase 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210422 MGI PMID:26851218 1620736 Sppl3 signal peptide peptidase 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20210422 MGI PMID:26851218 1620736 Sppl3 signal peptide peptidase 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1620736 Sppl3 signal peptide peptidase 3 gene MP:0013667 increased immature NK cell number IAGP N RGD:5509061 20210422 MGI PMID:26851218 1620736 Sppl3 signal peptide peptidase 3 gene MP:0013672 decreased mature NK cell number IAGP N RGD:5509061 20210422 MGI PMID:26851218 1620738 Nipal3 NIPA-like domain containing 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:19738379 1620738 Nipal3 NIPA-like domain containing 3 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:19738379 1620738 Nipal3 NIPA-like domain containing 3 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:19738379 1620738 Nipal3 NIPA-like domain containing 3 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:19738379 1620738 Nipal3 NIPA-like domain containing 3 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:19738379 1620738 Nipal3 NIPA-like domain containing 3 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:19738379 1620738 Nipal3 NIPA-like domain containing 3 gene MP:0005575 increased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:19738379 1620738 Nipal3 NIPA-like domain containing 3 gene MP:0005585 increased tidal volume IAGP N RGD:5509061 20141003 MGI PMID:19738379 1620738 Nipal3 NIPA-like domain containing 3 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19738379 1620738 Nipal3 NIPA-like domain containing 3 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:19738379 1620738 Nipal3 NIPA-like domain containing 3 gene MP:0014274 decreased respiration IAGP N RGD:5509061 20230810 MGI PMID:19738379 1620744 Fam53a family with sequence similarity 53, member A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1620744 Fam53a family with sequence similarity 53, member A gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1620744 Fam53a family with sequence similarity 53, member A gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1620744 Fam53a family with sequence similarity 53, member A gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 1620744 Fam53a family with sequence similarity 53, member A gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 1620744 Fam53a family with sequence similarity 53, member A gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1620744 Fam53a family with sequence similarity 53, member A gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1620744 Fam53a family with sequence similarity 53, member A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1620744 Fam53a family with sequence similarity 53, member A gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1620744 Fam53a family with sequence similarity 53, member A gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 1620744 Fam53a family with sequence similarity 53, member A gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20210826 MGI 1620744 Fam53a family with sequence similarity 53, member A gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210826 MGI 1620744 Fam53a family with sequence similarity 53, member A gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1620747 Ccdc103 coiled-coil domain containing 103 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1620747 Ccdc103 coiled-coil domain containing 103 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1620747 Ccdc103 coiled-coil domain containing 103 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 1620747 Ccdc103 coiled-coil domain containing 103 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20180201 MGI PMID:19460757 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:18437205 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:27480224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:15841208 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:18666258 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:18820241 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:19052228 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:22460046 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:26586440 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:15841208 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:16543947 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:18590693 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:18666258 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:26368306 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:26586440 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:18590693 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:20178984 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20180201 MGI PMID:23160527 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20180201 MGI PMID:23861731 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20180322 MGI PMID:28188211 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20191128 MGI PMID:23257357 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000199 abnormal circulating serum albumin level IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20180201 MGI PMID:16382155 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20221201 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:11171994 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:12697746 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:14613934 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:16467350 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:16977322 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:17464988 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:17567478 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:18434600 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:19234449 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:19551907 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:20080598 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:20080689 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:20404163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:20837017 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:22308354 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:23074225 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20180315 MGI PMID:28919113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20190912 MGI PMID:27311593 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20191128 MGI PMID:23257357 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210422 MGI PMID:32381628 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210603 MGI PMID:29116649 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210617 MGI PMID:33524375 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20221201 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:10938127 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:11171994 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:12566435 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:14769918 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:17567478 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:20080598 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:20404163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:21310927 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:21479224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:22308354 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:23074225 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20181129 MGI PMID:27032374 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20190912 MGI PMID:27311593 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000601 small liver IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000601 small liver IAGP N RGD:5509061 20180201 MGI PMID:21179166 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000601 small liver IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000601 small liver IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:10938127 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:12566435 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:12697746 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:14769918 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:17567478 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:19666474 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:22308354 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20190912 MGI PMID:27311593 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20180201 MGI PMID:19551907 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20180201 MGI PMID:22355113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20221229 MGI PMID:29967292 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:12482952 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:15082532 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:16467350 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:16977322 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:17567478 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:20080598 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:20080689 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:20404163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:20478530 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:20498273 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:21179166 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:21407177 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:21465509 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:21479224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:22355113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:23074225 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:23275615 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20190912 MGI PMID:27311593 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20210422 MGI PMID:32381628 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20221201 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20230608 MGI PMID:16382155 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20240328 MGI PMID:38194265 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180201 MGI PMID:16717184 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180201 MGI PMID:17646385 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180201 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180201 MGI PMID:21179166 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180201 MGI PMID:22308354 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180201 MGI PMID:23847050 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20180322 MGI PMID:28188211 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20190912 MGI PMID:27311593 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20191010 MGI PMID:30704899 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20210603 MGI PMID:29116649 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20240328 MGI PMID:38194265 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000610 cholestasis IAGP N RGD:5509061 20180201 MGI PMID:21310927 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000610 cholestasis IAGP N RGD:5509061 20180201 MGI PMID:25068656 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000611 jaundice IAGP N RGD:5509061 20180201 MGI PMID:18434600 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000611 jaundice IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000611 jaundice IAGP N RGD:5509061 20180315 MGI PMID:28919113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000611 jaundice IAGP N RGD:5509061 20181129 MGI PMID:27032374 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20180201 MGI PMID:22555437 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180201 MGI PMID:21310927 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001190 reddish skin IAGP N RGD:5509061 20180201 MGI PMID:16977322 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20180201 MGI PMID:16155866 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20180201 MGI PMID:18434600 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20210826 MGI PMID:34031390 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:11171994 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:17416680 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:18365007 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:19430492 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:23038251 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:25970332 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:26344103 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180201 MGI PMID:28244871 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20180201 MGI PMID:25068656 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20181129 MGI PMID:27032374 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:14613934 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:16155866 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:16977322 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:18365007 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:18434600 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:18590693 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:20829355 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:22308354 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190912 MGI PMID:27311593 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20181129 MGI PMID:27032374 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20180201 MGI PMID:22266220 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20180201 MGI PMID:25870278 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20180201 MGI PMID:23038251 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001426 polydipsia IAGP N RGD:5509061 20180201 MGI PMID:17416680 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20180201 MGI PMID:22555437 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20180201 MGI PMID:23038251 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20180201 MGI PMID:16717184 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20180201 MGI PMID:21407177 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20180201 MGI PMID:25806685 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:10938127 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:15841208 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:16155866 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:19889634 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:22460046 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:27480224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20210826 MGI PMID:34031390 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:10938127 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:16054078 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:16717184 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:19460757 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:21465509 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:27480224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20191128 MGI PMID:23257357 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20210826 MGI PMID:34031390 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:16964311 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:22555437 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:23275615 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20180201 MGI PMID:12529398 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20180201 MGI PMID:14613934 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20180201 MGI PMID:16717184 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20180201 MGI PMID:17416680 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20180201 MGI PMID:18590693 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20180201 MGI PMID:20348245 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20180201 MGI PMID:21720388 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20180201 MGI PMID:14613934 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20180201 MGI PMID:16467350 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001573 abnormal circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:20829355 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001577 anemia IAGP N RGD:5509061 20180201 MGI PMID:24520408 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20180201 MGI PMID:15798202 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20180201 MGI PMID:11171994 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20180201 MGI PMID:16977322 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20180201 MGI PMID:12697746 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20180201 MGI PMID:15738389 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20221201 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20180201 MGI PMID:18365007 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20180201 MGI PMID:20478530 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180201 MGI PMID:17464988 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20181129 MGI PMID:27032374 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20180201 MGI PMID:17416680 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20180201 MGI PMID:17464988 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20180201 MGI PMID:21479224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20180201 MGI PMID:22414809 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20180322 MGI PMID:28188211 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001775 abnormal selenium level IAGP N RGD:5509061 20180201 MGI PMID:23038251 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20180201 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20180201 MGI PMID:15070743 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180201 MGI PMID:15738389 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180201 MGI PMID:17567478 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180315 MGI PMID:28919113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200402 MGI PMID:31293973 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20210603 MGI PMID:29116649 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20221201 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20180201 MGI PMID:12566435 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20180201 MGI PMID:20375200 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20180201 MGI PMID:12566435 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:20080689 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20180201 MGI PMID:22355113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20210708 MGI PMID:33147459 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180201 MGI PMID:15821749 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180201 MGI PMID:16155866 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180201 MGI PMID:16717184 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180201 MGI PMID:20178984 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180201 MGI PMID:23160527 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180201 MGI PMID:9867845 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20191128 MGI PMID:23257357 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:16717184 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:17416680 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:18590692 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:18590693 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:19460757 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:20074531 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:21720388 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:27738106 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:9867845 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:11171994 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:16977322 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:17416680 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:17464988 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:22266220 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:22308354 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:23861731 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:24520408 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:25870278 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20181129 MGI PMID:27032374 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180201 MGI PMID:15821749 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180201 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180201 MGI PMID:19648649 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180201 MGI PMID:19889634 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180201 MGI PMID:22484817 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180201 MGI PMID:25806685 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180201 MGI PMID:27480224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180201 MGI PMID:28244871 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002139 abnormal hepatobiliary system physiology IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20180201 MGI PMID:23018454 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:10866673 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:12507915 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:20399150 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180201 MGI PMID:24316079 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240328 MGI PMID:38194265 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:16717184 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:20837017 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20180201 MGI PMID:21748766 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20180201 MGI PMID:21179166 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20180201 MGI PMID:26344103 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20180201 MGI PMID:16977322 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:11171994 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:12697746 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:14769918 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:15738389 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:15798202 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:16054078 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:16977322 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:17464988 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:17567478 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:18826952 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:19460757 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:19666474 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:20348245 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:20837017 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:21407177 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:22308354 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:25806685 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180201 MGI PMID:27738106 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20190912 MGI PMID:27311593 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20191010 MGI PMID:30704899 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20191128 MGI PMID:23257357 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20210826 MGI PMID:34031390 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20221201 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20240328 MGI PMID:38194265 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20180201 MGI PMID:16977322 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:12566435 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:15821749 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:18590693 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:19460757 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:19666474 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:20841350 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:21479224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:21720388 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:22484817 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:23275615 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:25806685 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:25970332 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:26344103 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:28244871 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20190912 MGI PMID:27311593 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20210422 MGI PMID:32381628 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002645 abnormal intestinal cholesterol absorption IAGP N RGD:5509061 20180201 MGI PMID:25378657 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20180201 MGI PMID:26586440 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002658 abnormal liver regeneration IAGP N RGD:5509061 20180201 MGI PMID:12482952 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20180201 MGI PMID:22555437 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20180201 MGI PMID:23038251 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:14769918 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:15821749 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:16717184 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:18590693 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:23275615 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:25970332 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20180201 MGI PMID:16054078 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20180201 MGI PMID:23160527 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002715 decreased glycogen catabolism rate IAGP N RGD:5509061 20180201 MGI PMID:20178984 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:12529398 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:14769918 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:15821749 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:16054078 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:16155866 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:20178984 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:20841350 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:22555437 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180201 MGI PMID:23160527 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20191128 MGI PMID:23257357 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20180201 MGI PMID:20375200 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20180201 MGI PMID:20178984 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002872 polycythemia IAGP N RGD:5509061 20180201 MGI PMID:11171994 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20180201 MGI PMID:14769918 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20180201 MGI PMID:15821749 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20180201 MGI PMID:20841350 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20180201 MGI PMID:23160527 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20180201 MGI PMID:24995976 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20181122 MGI PMID:24768164 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20190704 MGI PMID:28462079 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20191128 MGI PMID:23257357 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20180201 MGI PMID:18365007 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20180201 MGI PMID:18434600 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20180201 MGI PMID:19551907 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20180201 MGI PMID:20478530 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20180201 MGI PMID:19551907 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:12566435 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:14613934 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:15738389 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:17464988 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:17567478 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:18365007 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:18826952 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:20837017 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:21465509 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:25068656 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180315 MGI PMID:28919113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180322 MGI PMID:28188211 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200402 MGI PMID:31293973 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20221201 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:24995976 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20180201 MGI PMID:26586440 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20180201 MGI PMID:14613934 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20180201 MGI PMID:17567478 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20180201 MGI PMID:18365007 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20180201 MGI PMID:25068656 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20180201 MGI PMID:25970332 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20210422 MGI PMID:32381628 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:10938127 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:12697746 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:14769918 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:16054078 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:16977322 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:19460757 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:19551907 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:20080689 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:20348245 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:20404163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:21465509 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:22484817 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:25068656 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20191010 MGI PMID:30704899 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20210603 MGI PMID:29116649 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20210826 MGI PMID:34031390 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20221201 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003046 liver cirrhosis IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20180201 MGI PMID:16155866 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20180201 MGI PMID:17416680 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20180201 MGI PMID:9867845 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003066 increased liver copper level IAGP N RGD:5509061 20180201 MGI PMID:22216203 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003067 decreased liver copper level IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20180201 MGI PMID:16382155 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003106 abnormal fear-related response IAGP N RGD:5509061 20180201 MGI PMID:25870278 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003121 genetic imprinting IAGP N RGD:5509061 20180201 MGI PMID:12507915 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20180201 MGI PMID:16449639 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20190530 MGI PMID:24447392 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20180201 MGI PMID:24995976 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20180201 MGI PMID:25378657 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20180201 MGI PMID:25378657 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003195 calcinosis IAGP N RGD:5509061 20181122 MGI PMID:28592560 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003196 calcified skin IAGP N RGD:5509061 20181122 MGI PMID:28592560 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003252 abnormal bile duct physiology IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003252 abnormal bile duct physiology IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20180531 MGI PMID:29386660 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003254 bile duct inflammation IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20180201 MGI PMID:25068656 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20180315 MGI PMID:28919113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20180201 MGI PMID:15738389 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20180201 MGI PMID:17567478 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20180201 MGI PMID:19234449 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003325 decreased liver function IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003326 liver failure IAGP N RGD:5509061 20180201 MGI PMID:15070743 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003326 liver failure IAGP N RGD:5509061 20180201 MGI PMID:20436477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003326 liver failure IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:15738389 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:17567478 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:19234449 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:19878874 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:20080689 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:20837017 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:25132496 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:26131558 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20181129 MGI PMID:27032374 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180201 MGI PMID:15738389 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180201 MGI PMID:17567478 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180201 MGI PMID:21310927 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180201 MGI PMID:23508104 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180201 MGI PMID:25068656 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20180315 MGI PMID:28919113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20191010 MGI PMID:30704899 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20210603 MGI PMID:29116649 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20221201 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20180201 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20180201 MGI PMID:20178984 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20180201 MGI PMID:21720388 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20180201 MGI PMID:23861731 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20180201 MGI PMID:26344103 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20180201 MGI PMID:20178984 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20180315 MGI PMID:28919113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20180201 MGI PMID:22326219 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20180201 MGI PMID:23275615 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003457 abnormal circulating ketone body level IAGP N RGD:5509061 20180201 MGI PMID:20178984 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20180201 MGI PMID:16717184 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20180201 MGI PMID:23275615 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20191010 MGI PMID:30704899 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20190530 MGI PMID:24447392 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20180201 MGI PMID:20837017 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20180201 MGI PMID:25870278 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003707 increased cell nucleus count IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003839 abnormal insulin clearance IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003839 abnormal insulin clearance IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20180201 MGI PMID:25378657 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20210617 MGI PMID:33524375 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20180201 MGI PMID:14613934 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20180201 MGI PMID:15070743 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20180201 MGI PMID:20080598 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20180201 MGI PMID:20080689 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20180201 MGI PMID:20837017 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20180201 MGI PMID:21407177 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20210422 MGI PMID:32381628 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20221201 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20180201 MGI PMID:15070743 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:16977322 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:17567478 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:18026104 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:19551907 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:20080598 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:20080689 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:20478530 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:20837017 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:25004090 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:25068656 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20210422 MGI PMID:32381628 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20221201 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20221229 MGI PMID:29967292 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20230608 MGI PMID:16382155 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20190530 MGI PMID:24447392 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20180201 MGI PMID:19460757 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003927 increased cellular glucose import IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003943 abnormal hepatobiliary system development IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20210429 MGI PMID:33410752 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:25806685 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:25970332 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20180201 MGI PMID:23861731 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20180201 MGI PMID:25970332 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003981 decreased circulating phospholipid level IAGP N RGD:5509061 20180201 MGI PMID:25970332 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:25378657 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:26586440 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:19430492 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20180201 MGI PMID:22355113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004004 patent ductus venosus IAGP N RGD:5509061 20180201 MGI PMID:20829355 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004025 polyploidy IAGP N RGD:5509061 20180201 MGI PMID:22355113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004025 polyploidy IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004025 polyploidy IAGP N RGD:5509061 20221229 MGI PMID:29967292 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20180201 MGI PMID:22355113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20180315 MGI PMID:28919113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20180201 MGI PMID:15082532 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20180201 MGI PMID:19460757 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20180201 MGI PMID:25068656 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20180201 MGI PMID:18323469 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20210429 MGI PMID:33410752 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20210617 MGI PMID:33524375 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20180201 MGI PMID:12566435 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20180201 MGI PMID:25806685 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20180201 MGI PMID:15372107 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20180201 MGI PMID:23160527 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20180201 MGI PMID:25068656 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20180315 MGI PMID:28919113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20210429 MGI PMID:33410752 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20180201 MGI PMID:18590692 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20180201 MGI PMID:18590693 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20180531 MGI PMID:29386660 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20181129 MGI PMID:27032374 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0004898 uterine hemorrhage IAGP N RGD:5509061 20180201 MGI PMID:24520408 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20180201 MGI PMID:23018454 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180201 MGI PMID:23018454 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20180201 MGI PMID:23018454 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20180201 MGI PMID:19729839 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20180201 MGI PMID:16382155 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20180201 MGI PMID:20483735 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20180201 MGI PMID:23018454 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20180201 MGI PMID:19460757 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20180201 MGI PMID:19878874 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:22460046 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:26586440 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20180315 MGI PMID:28919113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20180201 MGI PMID:15070743 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20180201 MGI PMID:22355113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20180201 MGI PMID:25004090 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20180201 MGI PMID:19430492 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20180201 MGI PMID:23508104 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20190926 MGI PMID:30316865 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:16964311 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:12566435 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:12697746 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:15841208 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:16054078 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:18323469 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:18590693 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:18666258 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:18820241 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:21407177 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:22460046 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:22484817 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:25378657 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:26344103 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:26586440 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:28244871 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20190912 MGI PMID:27311593 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20180201 MGI PMID:20375200 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20180201 MGI PMID:23861731 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20180201 MGI PMID:24995976 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20180201 MGI PMID:15841208 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20180201 MGI PMID:22484817 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:14769918 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:27738106 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:16717184 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005283 increased unsaturated fatty acids level IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005284 increased saturated fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005285 decreased unsaturated fatty acids level IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005286 decreased saturated fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:16054078 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:22555437 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:14769918 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:15821749 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:18590693 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:20841350 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:23160527 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:26344103 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:15569412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:16155866 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:17416680 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:18590693 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:19460757 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:20074531 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:20178984 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:20348245 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:21479224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:21720388 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:27738106 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180201 MGI PMID:9867845 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20190530 MGI PMID:24447392 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210826 MGI PMID:34031390 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20180201 MGI PMID:23861731 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20180201 MGI PMID:25870278 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20180322 MGI PMID:28188211 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:16054078 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:26344103 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180201 MGI PMID:17416680 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180201 MGI PMID:18590692 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180201 MGI PMID:18590693 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180201 MGI PMID:20074531 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180201 MGI PMID:21479224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180201 MGI PMID:21720388 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180201 MGI PMID:27738106 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180201 MGI PMID:9867845 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20190530 MGI PMID:24447392 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20210826 MGI PMID:34031390 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20180201 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20180201 MGI PMID:16964311 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20180201 MGI PMID:22484817 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20180201 MGI PMID:26586440 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20180201 MGI PMID:14613934 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20180201 MGI PMID:17464988 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20180201 MGI PMID:18826952 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20180201 MGI PMID:23275615 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20180201 MGI PMID:25970332 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20180315 MGI PMID:28919113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200402 MGI PMID:31293973 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20221201 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20180201 MGI PMID:18365007 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20180201 MGI PMID:20478530 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20180201 MGI PMID:25068656 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20180315 MGI PMID:28919113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20180201 MGI PMID:17442273 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20180201 MGI PMID:25068656 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20180201 MGI PMID:26586440 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20210429 MGI PMID:33410752 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20180315 MGI PMID:28919113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20180201 MGI PMID:22266220 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20180201 MGI PMID:16155866 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005439 decreased glycogen level IAGP N RGD:5509061 20180201 MGI PMID:15821749 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005439 decreased glycogen level IAGP N RGD:5509061 20180201 MGI PMID:20178984 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005439 decreased glycogen level IAGP N RGD:5509061 20180201 MGI PMID:9867845 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005439 decreased glycogen level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20180201 MGI PMID:18437205 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20180201 MGI PMID:25004090 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20180201 MGI PMID:19052228 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20180201 MGI PMID:25004090 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20180201 MGI PMID:15372107 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20180201 MGI PMID:15070743 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20210415 MGI PMID:32518166 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:15569412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:16155866 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:18590693 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:9867845 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:14769918 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:15821749 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:16054078 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:17416680 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:19752163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:20178984 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:20841350 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:22326219 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:23160527 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:26344103 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20181122 MGI PMID:24768164 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20180201 MGI PMID:23275615 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20180201 MGI PMID:23038251 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180201 MGI PMID:12697746 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180201 MGI PMID:16467350 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180201 MGI PMID:16717184 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180201 MGI PMID:20375200 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180809 MGI PMID:27208177 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20180201 MGI PMID:24520408 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20180201 MGI PMID:16122419 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20180201 MGI PMID:16382155 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20180201 MGI PMID:18323469 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20180201 MGI PMID:24995976 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20180201 MGI PMID:26586440 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20180201 MGI PMID:21310927 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20180201 MGI PMID:21748766 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005638 hemochromatosis IAGP N RGD:5509061 20180201 MGI PMID:21748766 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20180201 MGI PMID:16467350 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180201 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20180201 MGI PMID:14769918 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20180201 MGI PMID:17464988 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20210708 MGI PMID:33147459 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180201 MGI PMID:17464988 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180201 MGI PMID:20691904 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180201 MGI PMID:24995976 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180201 MGI PMID:26344103 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20180322 MGI PMID:28188211 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20180201 MGI PMID:15798202 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0006084 abnormal circulating phospholipid level IAGP N RGD:5509061 20180201 MGI PMID:15841208 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20180201 MGI PMID:20178984 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008007 abnormal cellular replicative senescence IAGP N RGD:5509061 20180201 MGI PMID:23508104 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20180201 MGI PMID:20080689 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20180201 MGI PMID:20837017 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20181129 MGI PMID:27032374 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20210603 MGI PMID:29116649 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20180201 MGI PMID:24520408 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20180201 MGI PMID:14769918 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20191128 MGI PMID:23257357 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20180201 MGI PMID:23018454 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20180201 MGI PMID:23018454 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20221229 MGI PMID:29967292 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20180201 MGI PMID:22308354 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20180201 MGI PMID:16964311 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20180201 MGI PMID:24302768 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20180201 MGI PMID:24302768 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20180809 MGI PMID:27208177 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20210415 MGI PMID:32518166 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008805 decreased circulating amylase level IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20180201 MGI PMID:21748766 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20180201 MGI PMID:21748766 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20180201 MGI PMID:21748766 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180201 MGI PMID:16382155 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20221201 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180201 MGI PMID:16293230 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180201 MGI PMID:16301529 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180201 MGI PMID:20829355 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180201 MGI PMID:22484817 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20190207 MGI PMID:24731446 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20180201 MGI PMID:12566435 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20180201 MGI PMID:18805792 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20180201 MGI PMID:16054078 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20180201 MGI PMID:21575863 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008987 abnormal liver lobule morphology IAGP N RGD:5509061 20180201 MGI PMID:23074225 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20180201 MGI PMID:20080689 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20180201 MGI PMID:20498273 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008990 abnormal Ito cell morphology IAGP N RGD:5509061 20221201 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008991 abnormal bile canaliculus morphology IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008991 abnormal bile canaliculus morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008992 abnormal portal lobule morphology IAGP N RGD:5509061 20180201 MGI PMID:20404163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0008993 abnormal portal triad morphology IAGP N RGD:5509061 20210603 MGI PMID:29116649 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20180201 MGI PMID:23160527 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20180201 MGI PMID:15372107 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20180201 MGI PMID:17416680 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20180614 MGI PMID:23160527 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20180614 MGI PMID:15372107 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009122 decreased white fat cell lipid droplet size IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009138 increased brown fat lipid droplet number IAGP N RGD:5509061 20180322 MGI PMID:28188211 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20180201 MGI PMID:23160527 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20180201 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20180201 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20180201 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009342 enlarged gallbladder IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:10938127 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:14769918 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:17567478 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:19666474 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:20178984 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:20348245 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:21407177 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:21465509 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:25806685 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:27480224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:27738106 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20190912 MGI PMID:27311593 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20191010 MGI PMID:30704899 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20191128 MGI PMID:23257357 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20210826 MGI PMID:34031390 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:16717184 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:19460757 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:21720388 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:22460046 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:24458359 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20180201 MGI PMID:28244871 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20180201 MGI PMID:17464988 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20180201 MGI PMID:23275615 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009497 abnormal intrahepatic bile duct morphology IAGP N RGD:5509061 20180201 MGI PMID:19551907 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009501 abnormal hepatic duct morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20180201 MGI PMID:16054078 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20180201 MGI PMID:16122419 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20180201 MGI PMID:22414809 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20180201 MGI PMID:24719406 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20180201 MGI PMID:12697746 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180201 MGI PMID:25068656 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20180201 MGI PMID:21385828 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20180201 MGI PMID:16293230 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20180201 MGI PMID:21385828 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20180201 MGI PMID:20837017 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20180201 MGI PMID:14769918 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20180201 MGI PMID:16054078 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20180201 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20191128 MGI PMID:23257357 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:16054078 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:21720388 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:22460046 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:27480224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:28244871 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20210429 MGI PMID:33410752 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20210617 MGI PMID:33524375 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:17567478 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:19666474 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:22484817 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:25806685 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:26586440 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20180201 MGI PMID:27480224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20190912 MGI PMID:27311593 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010040 abnormal oval cell morphology IAGP N RGD:5509061 20180201 MGI PMID:20404163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010042 abnormal oval cell physiology IAGP N RGD:5509061 20180201 MGI PMID:20404163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010042 abnormal oval cell physiology IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010042 abnormal oval cell physiology IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010076 abnormal phytosterol level IAGP N RGD:5509061 20180201 MGI PMID:25378657 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010078 increased circulating phytosterol level IAGP N RGD:5509061 20180201 MGI PMID:25378657 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20180201 MGI PMID:15070743 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20180201 MGI PMID:19889634 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20180201 MGI PMID:20498273 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20180201 MGI PMID:21479224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20180201 MGI PMID:23861731 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20180201 MGI PMID:25621497 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20210422 MGI PMID:32381628 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20230608 MGI PMID:16382155 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20240530 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010244 decreased kidney copper level IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20180201 MGI PMID:20404163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010266 decreased liver tumor incidence IAGP N RGD:5509061 20180201 MGI PMID:15082532 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010297 increased hepatobiliary system tumor incidence IAGP N RGD:5509061 20180201 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010297 increased hepatobiliary system tumor incidence IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20180201 MGI PMID:22266220 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:20837017 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:22266220 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20180531 MGI PMID:29386660 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20181129 MGI PMID:27032374 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010331 abnormal apolipoprotein level IAGP N RGD:5509061 20180201 MGI PMID:21407177 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010331 abnormal apolipoprotein level IAGP N RGD:5509061 20180201 MGI PMID:25970332 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010332 abnormal circulating apolipoprotein level IAGP N RGD:5509061 20180201 MGI PMID:25806685 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:27480224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010360 decreased liver free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:21720388 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010360 decreased liver free fatty acids level IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010360 decreased liver free fatty acids level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010360 decreased liver free fatty acids level IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20191128 MGI PMID:23257357 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20180201 MGI PMID:24458359 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20180201 MGI PMID:26344103 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20190530 MGI PMID:24447392 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20180201 MGI PMID:18434600 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20180201 MGI PMID:22308354 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20180201 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20180201 MGI PMID:27738106 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20190704 MGI PMID:28462079 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191128 MGI PMID:23257357 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:10938127 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:16155866 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:18354499 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:18590693 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20180201 MGI PMID:14769918 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20191010 MGI PMID:30704899 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010951 abnormal lipid oxidation IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010952 abnormal fatty acid beta-oxidation IAGP N RGD:5509061 20180201 MGI PMID:17442273 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010953 abnormal fatty acid oxidation IAGP N RGD:5509061 20180201 MGI PMID:24458359 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010953 abnormal fatty acid oxidation IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20180201 MGI PMID:24995976 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20180322 MGI PMID:28188211 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20180201 MGI PMID:18437205 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20180201 MGI PMID:23847050 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20180201 MGI PMID:20691904 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20180201 MGI PMID:14749836 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20180201 MGI PMID:18437205 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20210415 MGI PMID:32518166 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011017 increased body surface temperature IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:18434600 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011424 decreased urine uric acid level IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011582 decreased triglyceride lipase activity IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011582 decreased triglyceride lipase activity IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20180315 MGI PMID:28919113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20180201 MGI PMID:25683716 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20190530 MGI PMID:24447392 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20180201 MGI PMID:17464988 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20180201 MGI PMID:10949030 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011634 abnormal mitochondrial inner membrane morphology IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20180201 MGI PMID:20691904 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20180201 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20190530 MGI PMID:24447392 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011770 increased urine selenium level IAGP N RGD:5509061 20180201 MGI PMID:23038251 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20180201 MGI PMID:21748766 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011897 decreased circulating unsaturated transferrin level IAGP N RGD:5509061 20180201 MGI PMID:21748766 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011897 decreased circulating unsaturated transferrin level IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20190530 MGI PMID:24447392 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210211 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210218 MGI PMID:14613934 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20180201 MGI PMID:20178984 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0012224 abnormal sterol level IAGP N RGD:5509061 20180201 MGI PMID:25176150 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0012224 abnormal sterol level IAGP N RGD:5509061 20210429 MGI PMID:33410752 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0012224 abnormal sterol level IAGP N RGD:5509061 20210617 MGI PMID:33524375 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0012236 abnormal cholangiocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:21465509 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0012236 abnormal cholangiocyte morphology IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0012242 abnormal hepatoblast differentiation IAGP N RGD:5509061 20180201 MGI PMID:18434600 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0012246 abnormal hepatic cord morphology IAGP N RGD:5509061 20180201 MGI PMID:20498273 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0012246 abnormal hepatic cord morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0012338 decreased bile salt level IAGP N RGD:5509061 20180201 MGI PMID:26586440 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0012356 increased prothrombin time IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0012359 increased partial thromboplastin time IAGP N RGD:5509061 20180201 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0012691 abnormal acetaminophen metabolism IAGP N RGD:5509061 20180201 MGI PMID:12566435 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013119 abdomen swellings IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20181129 MGI PMID:27032374 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013243 abnormal carbohydrate metabolism IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20180322 MGI PMID:28188211 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20190704 MGI PMID:28462079 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20191128 MGI PMID:23257357 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20180201 MGI PMID:27738106 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20180920 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20190530 MGI PMID:24447392 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20191017 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20180201 MGI PMID:15732085 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20180201 MGI PMID:26344103 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013437 decreased phytosterol level IAGP N RGD:5509061 20180201 MGI PMID:25378657 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0013611 abnormal bile duct epithelium morphology IAGP N RGD:5509061 20210708 MGI PMID:33513427 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014038 increased hepatocyte number IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014038 increased hepatocyte number IAGP N RGD:5509061 20180201 MGI PMID:26699479 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014045 Mallory bodies IAGP N RGD:5509061 20180201 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014045 Mallory bodies IAGP N RGD:5509061 20180201 MGI PMID:17567478 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20180201 MGI PMID:18437205 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014109 increased pancreatic alpha cell proliferation IAGP N RGD:5509061 20180614 MGI PMID:23160527 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20210422 MGI PMID:33177714 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20180201 MGI PMID:22231784 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20180201 MGI PMID:26344103 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20180201 MGI PMID:21465509 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20180201 MGI PMID:23299886 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20180201 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014174 decreased fatty acid beta-oxidation IAGP N RGD:5509061 20180201 MGI PMID:27738106 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:16467350 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:21907140 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:23074225 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:23861731 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:28188211 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014391 increased hepatocyte mitochondrial DNA content IAGP N RGD:5509061 20240328 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014476 abnormal feces lipid level IAGP N RGD:5509061 20240704 MGI PMID:25176150 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0014480 increased feces cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:26586440 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0020103 decreased hepatic glucose production IAGP N RGD:5509061 20180201 MGI PMID:25043815 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0020211 slow movement IAGP N RGD:5509061 20180315 MGI PMID:28919113 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0020215 impaired blood coagulation IAGP N RGD:5509061 20180201 MGI PMID:24520408 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20180201 MGI PMID:21465509 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20180201 MGI PMID:15070743 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20180201 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20200402 MGI PMID:31293973 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20210422 MGI PMID:32381628 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20221201 MGI PMID:26458163 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20221229 MGI PMID:29967292 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0020867 increased lipogenesis IAGP N RGD:5509061 20210826 MGI PMID:34031390 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0021045 decreased circulating VLDL phospholipid level IAGP N RGD:5509061 20220106 MGI PMID:25806685 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030020 decreased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20180201 MGI PMID:20178984 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030533 abnormal snout skin morphology IAGP N RGD:5509061 20181122 MGI PMID:28592560 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030599 decreased liver manganese level IAGP N RGD:5509061 20180809 MGI PMID:27208177 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030623 decreased cysteine level IAGP N RGD:5509061 20180920 MGI PMID:22414809 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030626 decreased circulating cysteine level IAGP N RGD:5509061 20180920 MGI PMID:22414809 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030644 increased circulating methionine level IAGP N RGD:5509061 20180920 MGI PMID:28188211 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030667 increased circulating proline level IAGP N RGD:5509061 20180920 MGI PMID:28188211 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030694 increased circulating serine level IAGP N RGD:5509061 20180927 MGI PMID:28188211 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030703 increased circulating threonine level IAGP N RGD:5509061 20180927 MGI PMID:28188211 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030718 increased circulating lysine level IAGP N RGD:5509061 20180927 MGI PMID:28188211 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20190711 MGI PMID:27689697 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:23074225 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20191010 MGI PMID:30704899 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030951 abnormal endocytosis IAGP N RGD:5509061 20211118 MGI PMID:27374329 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030973 impaired gluconeogenesis IAGP N RGD:5509061 20200130 MGI PMID:31597092 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030973 impaired gluconeogenesis IAGP N RGD:5509061 20200409 MGI PMID:30639734 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0030973 impaired gluconeogenesis IAGP N RGD:5509061 20230119 MGI PMID:36441025 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:12566435 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:20643348 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21465509 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21479224 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:25970332 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:12566435 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:15199412 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:16977322 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21465509 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:22820288 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:23733885 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:25448926 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031137 vaginal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:24520408 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031152 subcutaneous hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:24520408 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031252 abnormal physiological response to hypoxia IAGP N RGD:5509061 20210708 MGI PMID:33147459 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:18054317 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:24995976 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:28508477 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:30582764 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20231012 MGI PMID:37524868 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031269 increased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210826 MGI PMID:34031390 1620748 Speer6-ps1 spermatogenesis associated glutamate (E)-rich protein 6, pseudogene 1 gene MP:0031270 decreased susceptibility to age-related hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:22231784 1620750 Cib4 calcium and integrin binding family member 4 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200924 MGI PMID:32430498 1620750 Cib4 calcium and integrin binding family member 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20200924 MGI PMID:32430498 1620750 Cib4 calcium and integrin binding family member 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20240523 MGI 1620750 Cib4 calcium and integrin binding family member 4 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 1620750 Cib4 calcium and integrin binding family member 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200924 MGI PMID:32430498 1620750 Cib4 calcium and integrin binding family member 4 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20200924 MGI PMID:32430498 1620750 Cib4 calcium and integrin binding family member 4 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20200924 MGI PMID:32430498 1620753 Setd7 SET domain containing (lysine methyltransferase) 7 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20170406 MGI PMID:27292644 1620753 Setd7 SET domain containing (lysine methyltransferase) 7 gene MP:0002333 abnormal lung compliance IAGP N RGD:5509061 20170406 MGI PMID:27292644 1620753 Setd7 SET domain containing (lysine methyltransferase) 7 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:18280244 1620753 Setd7 SET domain containing (lysine methyltransferase) 7 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20170406 MGI PMID:27292644 1620753 Setd7 SET domain containing (lysine methyltransferase) 7 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20170406 MGI PMID:27292644 1620753 Setd7 SET domain containing (lysine methyltransferase) 7 gene MP:0008737 abnormal spleen physiology IAGP N RGD:5509061 20141003 MGI PMID:18280244 1620753 Setd7 SET domain containing (lysine methyltransferase) 7 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18280244 1620753 Setd7 SET domain containing (lysine methyltransferase) 7 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20170406 MGI PMID:27292644 1620753 Setd7 SET domain containing (lysine methyltransferase) 7 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:18280244 1620753 Setd7 SET domain containing (lysine methyltransferase) 7 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18280244 1620753 Setd7 SET domain containing (lysine methyltransferase) 7 gene MP:0013258 abnormal extracellular matrix morphology IAGP N RGD:5509061 20170406 MGI PMID:27292644 1620754 Ceacam5 CEA cell adhesion molecule 5 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1620754 Ceacam5 CEA cell adhesion molecule 5 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1620754 Ceacam5 CEA cell adhesion molecule 5 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1620757 Fam118a family with sequence similarity 118, member A gene MP:0005333 decreased heart rate IEA N RGD:5509061 20240523 MGI 1620757 Fam118a family with sequence similarity 118, member A gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20231207 MGI 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20160714 MGI PMID:27112497 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20160714 MGI PMID:27112497 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0000599 enlarged liver IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160714 MGI PMID:27112497 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20160317 MGI 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0001147 small testis IEA N RGD:5509061 20231207 MGI 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0001194 dermatitis IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160714 MGI PMID:27112497 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160714 MGI PMID:27112497 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0001393 ataxia IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160714 MGI PMID:27112497 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0001847 brain inflammation IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0001860 liver inflammation IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0001953 respiratory failure IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0002083 premature death IAGP N RGD:5509061 20160714 MGI PMID:27112497 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0002083 premature death IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0002351 abnormal cervical lymph node morphology IAGP N RGD:5509061 20160714 MGI PMID:27112497 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0002451 abnormal macrophage physiology IEA N RGD:5509061 20160317 MGI 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0002493 increased IgG level IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0002494 increased IgM level IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20160714 MGI PMID:27112497 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0003691 abnormal microglial cell physiology IEA N RGD:5509061 20160317 MGI 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0003960 increased lean body mass IEA N RGD:5509061 20231207 MGI 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20231207 MGI 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0004952 increased spleen weight IEA N RGD:5509061 20231207 MGI 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20160714 MGI PMID:27112497 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0005059 lysosomal protein accumulation IEA N RGD:5509061 20160317 MGI 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0005150 cachexia IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0008027 abnormal spinal cord white matter morphology IEA N RGD:5509061 20160317 MGI 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0008503 abnormal spinal cord grey matter morphology IEA N RGD:5509061 20160317 MGI 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0008542 enlarged cervical lymph nodes IAGP N RGD:5509061 20160714 MGI PMID:27112497 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0008542 enlarged cervical lymph nodes IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0008600 decreased circulating interleukin-2 level IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20160714 MGI PMID:27112497 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0009626 abnormal celiac lymph node morphology IAGP N RGD:5509061 20160714 MGI PMID:27112497 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20231207 MGI 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620759 C9orf72 C9orf72, member of C9orf72-SMCR8 complex gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20190228 MGI PMID:27412785 1620762 Slc25a35 solute carrier family 25, member 35 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220519 MGI 1620763 Esco2 establishment of sister chromatid cohesion N-acetyltransferase 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:22101327 1620763 Esco2 establishment of sister chromatid cohesion N-acetyltransferase 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20200310 MGI PMID:22101327 1620763 Esco2 establishment of sister chromatid cohesion N-acetyltransferase 2 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20200310 MGI PMID:22101327 1620763 Esco2 establishment of sister chromatid cohesion N-acetyltransferase 2 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20200310 MGI PMID:22101327 1620763 Esco2 establishment of sister chromatid cohesion N-acetyltransferase 2 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20200310 MGI PMID:22101327 1620763 Esco2 establishment of sister chromatid cohesion N-acetyltransferase 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:22101327 1620763 Esco2 establishment of sister chromatid cohesion N-acetyltransferase 2 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20200310 MGI PMID:22101327 1620763 Esco2 establishment of sister chromatid cohesion N-acetyltransferase 2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200310 MGI PMID:22101327 1620763 Esco2 establishment of sister chromatid cohesion N-acetyltransferase 2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20211216 MGI PMID:32555289 1620763 Esco2 establishment of sister chromatid cohesion N-acetyltransferase 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:22101327 1620763 Esco2 establishment of sister chromatid cohesion N-acetyltransferase 2 gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20200310 MGI PMID:22101327 1620763 Esco2 establishment of sister chromatid cohesion N-acetyltransferase 2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20200310 MGI PMID:22101327 1620763 Esco2 establishment of sister chromatid cohesion N-acetyltransferase 2 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20200310 MGI PMID:22101327 1620763 Esco2 establishment of sister chromatid cohesion N-acetyltransferase 2 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20200310 MGI PMID:22101327 1620763 Esco2 establishment of sister chromatid cohesion N-acetyltransferase 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22101327 1620764 Acad10 acyl-Coenzyme A dehydrogenase family, member 10 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1620767 Wdr73 WD repeat domain 73 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1620767 Wdr73 WD repeat domain 73 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20240919 MGI 1620767 Wdr73 WD repeat domain 73 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1620767 Wdr73 WD repeat domain 73 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1620768 Tom1l1 target of myb1-like 1 (chicken) gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1620769 Apol6 apolipoprotein L 6 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620769 Apol6 apolipoprotein L 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620769 Apol6 apolipoprotein L 6 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620769 Apol6 apolipoprotein L 6 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620769 Apol6 apolipoprotein L 6 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620769 Apol6 apolipoprotein L 6 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620769 Apol6 apolipoprotein L 6 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620769 Apol6 apolipoprotein L 6 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620769 Apol6 apolipoprotein L 6 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620769 Apol6 apolipoprotein L 6 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620769 Apol6 apolipoprotein L 6 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620769 Apol6 apolipoprotein L 6 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620769 Apol6 apolipoprotein L 6 gene MP:0009303 decreased renal fat pad weight IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620769 Apol6 apolipoprotein L 6 gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620769 Apol6 apolipoprotein L 6 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620769 Apol6 apolipoprotein L 6 gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20240229 MGI PMID:38167864 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20220811 MGI 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191128 MGI 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191128 MGI 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20240620 MGI PMID:35726782 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20240620 MGI PMID:35726782 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20240620 MGI PMID:35726782 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191128 MGI 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20240620 MGI PMID:35726782 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20240620 MGI PMID:35726782 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20240620 MGI PMID:35726782 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20240620 MGI PMID:35726782 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191128 MGI 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0010126 abnormal distal visceral endoderm morphology IAGP N RGD:5509061 20240620 MGI PMID:35726782 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20240620 MGI PMID:35726782 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20240620 MGI PMID:35726782 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20240620 MGI PMID:35726782 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0011192 decreased embryonic epiblast cell proliferation IAGP N RGD:5509061 20240620 MGI PMID:35726782 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0012724 absent head fold IEA N RGD:5509061 20191128 MGI 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191128 MGI 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20240620 MGI PMID:35726782 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20240620 MGI PMID:35726782 1620771 Borcs6 BLOC-1 related complex subunit 6 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20240620 MGI PMID:35726782 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20231207 MGI 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20231207 MGI 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20220721 MGI PMID:34376666 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20220721 MGI PMID:34376666 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20220721 MGI PMID:34376666 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20220721 MGI PMID:34376666 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20220721 MGI PMID:34376666 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20231207 MGI 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0013792 abnormal small intestine goblet cell morphology IAGP N RGD:5509061 20220721 MGI PMID:34376666 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0013958 decreased small intestine length IAGP N RGD:5509061 20220721 MGI PMID:34376666 1620772 Rpap3 RNA polymerase II associated protein 3 gene MP:0014201 abnormal intestinal epithelium physiology IAGP N RGD:5509061 20220721 MGI PMID:34376666 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:22529944 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0001135 abnormal uterine cervix morphology IAGP N RGD:5509061 20141003 MGI PMID:22529944 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19617532 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:22529944 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0004038 lymphangiectasis IAGP N RGD:5509061 20141003 MGI PMID:22529944 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:22529944 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22529944 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:22529944 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:22529944 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:19617532 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0009209 abnormal internal female genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:22529944 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20141003 MGI PMID:22529944 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19617532 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19617532 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0012010 parturition failure IAGP N RGD:5509061 20141003 MGI PMID:22529944 1620775 Antxr2 anthrax toxin receptor 2 gene MP:0031434 increased miscarriage rate IAGP N RGD:5509061 20220915 MGI PMID:22529944 1620777 Jsrp1 junctional sarcoplasmic reticulum protein 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:18077436 1620777 Jsrp1 junctional sarcoplasmic reticulum protein 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:18077436 1620777 Jsrp1 junctional sarcoplasmic reticulum protein 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:18077436 1620778 Ces2f carboxylesterase 2F gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20160929 MGI PMID:27534441 1620778 Ces2f carboxylesterase 2F gene MP:0005505 thrombocytosis IEA N RGD:5509061 20211021 MGI 1620778 Ces2f carboxylesterase 2F gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1620779 Fam219a family with sequence similarity 219, member A gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1620779 Fam219a family with sequence similarity 219, member A gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210520 MGI 1620779 Fam219a family with sequence similarity 219, member A gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210520 MGI 1620779 Fam219a family with sequence similarity 219, member A gene MP:0001262 decreased body weight IEA N RGD:5509061 20210826 MGI 1620779 Fam219a family with sequence similarity 219, member A gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20210520 MGI 1620779 Fam219a family with sequence similarity 219, member A gene MP:0010935 increased airway resistance IEA N RGD:5509061 20240523 MGI 1620780 Nup205 nucleoporin 205 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240919 MGI 1620780 Nup205 nucleoporin 205 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220519 MGI 1620780 Nup205 nucleoporin 205 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 1620780 Nup205 nucleoporin 205 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1620780 Nup205 nucleoporin 205 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241017 MGI 1620780 Nup205 nucleoporin 205 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20200402 MGI 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:24311790 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20200402 MGI 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20200402 MGI 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:24311790 1620783 Dusp16 dual specificity phosphatase 16 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24311790 1620784 Utp20 UTP20 small subunit processome component gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20201022 MGI 1620784 Utp20 UTP20 small subunit processome component gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1620784 Utp20 UTP20 small subunit processome component gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1620784 Utp20 UTP20 small subunit processome component gene MP:0002080 prenatal lethality IEA N RGD:5509061 20210128 MGI 1620784 Utp20 UTP20 small subunit processome component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620785 Prdm16 PR domain containing 16 gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0000097 short maxilla IAGP N RGD:5509061 20171019 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20111116 MGI 1620785 Prdm16 PR domain containing 16 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20220804 MGI PMID:34915728 1620785 Prdm16 PR domain containing 16 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0000448 pointed snout IAGP N RGD:5509061 20171019 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0001258 decreased body length IAGP N RGD:5509061 20180111 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180111 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20220804 MGI PMID:34915728 1620785 Prdm16 PR domain containing 16 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20220804 MGI PMID:34915728 1620785 Prdm16 PR domain containing 16 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20180111 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0003416 premature bone ossification IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20180111 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0004035 abnormal sublingual gland morphology IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20220804 MGI PMID:34915728 1620785 Prdm16 PR domain containing 16 gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20180111 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180111 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20220804 MGI PMID:34915728 1620785 Prdm16 PR domain containing 16 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0006320 abnormal interscapular fat pad morphology IAGP N RGD:5509061 20180111 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20180111 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0009137 decreased brown fat lipid droplet number IAGP N RGD:5509061 20180111 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20180111 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0009522 submandibular gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0009525 abnormal submandibular duct morphology IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0009527 abnormal sublingual duct morphology IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:11818962 1620785 Prdm16 PR domain containing 16 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20220804 MGI PMID:34915728 1620785 Prdm16 PR domain containing 16 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20220804 MGI PMID:34915728 1620785 Prdm16 PR domain containing 16 gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20180111 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20220804 MGI PMID:34915728 1620785 Prdm16 PR domain containing 16 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0011089 perinatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1620785 Prdm16 PR domain containing 16 gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1620785 Prdm16 PR domain containing 16 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20220804 MGI PMID:34915728 1620785 Prdm16 PR domain containing 16 gene MP:0011615 submucous cleft palate IAGP N RGD:5509061 20141003 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20180111 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20220804 MGI PMID:34915728 1620785 Prdm16 PR domain containing 16 gene MP:0012515 abnormal heart apex morphology IAGP N RGD:5509061 20220804 MGI PMID:34915728 1620785 Prdm16 PR domain containing 16 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20180111 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0014396 decreased fat cell mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0020520 whitened brown adipose tissue morphology IAGP N RGD:5509061 20180208 MGI PMID:24703692 1620785 Prdm16 PR domain containing 16 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:24439384 1620785 Prdm16 PR domain containing 16 gene MP:0030191 narrow snout IAGP N RGD:5509061 20171019 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0030248 narrow maxilla IAGP N RGD:5509061 20171019 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:20007998 1620785 Prdm16 PR domain containing 16 gene MP:0031525 thin left ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:34915728 1620789 Dnajb14 DnaJ heat shock protein family (Hsp40) member B14 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1620789 Dnajb14 DnaJ heat shock protein family (Hsp40) member B14 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20221215 MGI 1620789 Dnajb14 DnaJ heat shock protein family (Hsp40) member B14 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1620789 Dnajb14 DnaJ heat shock protein family (Hsp40) member B14 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1620789 Dnajb14 DnaJ heat shock protein family (Hsp40) member B14 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1620789 Dnajb14 DnaJ heat shock protein family (Hsp40) member B14 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1620789 Dnajb14 DnaJ heat shock protein family (Hsp40) member B14 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620790 Ecd ecdysoneless cell cycle regulator gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19640839 1620798 H2bl1 H2B.L histone variant 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1620802 Smco2 single-pass membrane protein with coiled-coil domains 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1620804 Wdfy1 WD repeat and FYVE domain containing 1 gene MP:0002626 increased heart rate IEA N RGD:5509061 20210826 MGI 1620804 Wdfy1 WD repeat and FYVE domain containing 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1620804 Wdfy1 WD repeat and FYVE domain containing 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1620804 Wdfy1 WD repeat and FYVE domain containing 1 gene MP:0010507 shortened RR interval IEA N RGD:5509061 20230601 MGI 1620805 Cfap107 cilia and flagella associated protein 107 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1620806 Spaca4 sperm acrosome associated 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20211021 MGI PMID:34556579 1620806 Spaca4 sperm acrosome associated 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20211021 MGI PMID:34556579 1620806 Spaca4 sperm acrosome associated 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20211021 MGI PMID:34556579 1620806 Spaca4 sperm acrosome associated 4 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20211021 MGI PMID:34556579 1620806 Spaca4 sperm acrosome associated 4 gene MP:0031009 abnormal sperm-egg fusion IAGP N RGD:5509061 20211021 MGI PMID:34556579 1620809 1700008P02Rik RIKEN cDNA 1700008P02 gene gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1620809 1700008P02Rik RIKEN cDNA 1700008P02 gene gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20230601 MGI 1620809 1700008P02Rik RIKEN cDNA 1700008P02 gene gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1620809 1700008P02Rik RIKEN cDNA 1700008P02 gene gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210826 MGI 1620813 1700012B09Rik RIKEN cDNA 1700012B09 gene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190221 MGI PMID:28666954 1620813 1700012B09Rik RIKEN cDNA 1700012B09 gene gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20191128 MGI 1620816 Fam24b family with sequence similarity 24 member B gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1620816 Fam24b family with sequence similarity 24 member B gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1620816 Fam24b family with sequence similarity 24 member B gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1620817 Izumo3 IZUMO family member 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220721 MGI PMID:34114279 1620817 Izumo3 IZUMO family member 3 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220721 MGI PMID:34114279 1620818 Ppp1r42 protein phosphatase 1, regulatory subunit 42 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20170105 MGI 1620818 Ppp1r42 protein phosphatase 1, regulatory subunit 42 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240627 MGI PMID:38835510 1620819 Pacrg PARK2 co-regulated gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1620819 Pacrg PARK2 co-regulated gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 1620819 Pacrg PARK2 co-regulated gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1620819 Pacrg PARK2 co-regulated gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1620821 Efcab9 EF-hand calcium binding domain 9 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20201224 MGI PMID:31056283 1620821 Efcab9 EF-hand calcium binding domain 9 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20201224 MGI PMID:31056283 1620821 Efcab9 EF-hand calcium binding domain 9 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20201224 MGI PMID:31056283 1620821 Efcab9 EF-hand calcium binding domain 9 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20201224 MGI PMID:31056283 1620821 Efcab9 EF-hand calcium binding domain 9 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20201224 MGI PMID:31056283 1620821 Efcab9 EF-hand calcium binding domain 9 gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20220714 MGI PMID:31056283 1620823 Lurap1 leucine rich adaptor protein 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20210128 MGI 1620823 Lurap1 leucine rich adaptor protein 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1620823 Lurap1 leucine rich adaptor protein 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1620823 Lurap1 leucine rich adaptor protein 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1620824 Mrnip MRN complex interacting protein gene MP:0001147 small testis IAGP N RGD:5509061 20210603 MGI PMID:33689881 1620824 Mrnip MRN complex interacting protein gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20210603 MGI PMID:33689881 1620824 Mrnip MRN complex interacting protein gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20210603 MGI PMID:33689881 1620824 Mrnip MRN complex interacting protein gene MP:0001399 hyperactivity IEA N RGD:5509061 20160804 MGI 1620824 Mrnip MRN complex interacting protein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210603 MGI PMID:33689881 1620824 Mrnip MRN complex interacting protein gene MP:0001935 decreased litter size IAGP N RGD:5509061 20210603 MGI PMID:33689881 1620824 Mrnip MRN complex interacting protein gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210603 MGI PMID:33689881 1620824 Mrnip MRN complex interacting protein gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210603 MGI PMID:33689881 1620824 Mrnip MRN complex interacting protein gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210603 MGI PMID:33689881 1620824 Mrnip MRN complex interacting protein gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20210603 MGI PMID:33689881 1620824 Mrnip MRN complex interacting protein gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20210603 MGI PMID:33689881 1620824 Mrnip MRN complex interacting protein gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20210603 MGI PMID:33689881 1620825 Slc25a39 solute carrier family 25, member 39 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1620825 Slc25a39 solute carrier family 25, member 39 gene MP:0001513 limb grasping IEA N RGD:5509061 20230601 MGI 1620825 Slc25a39 solute carrier family 25, member 39 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1620825 Slc25a39 solute carrier family 25, member 39 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20231207 MGI 1620826 Dmac2l distal membrane arm assembly component 2 like gene MP:0005287 narrow eye opening IEA N RGD:5509061 20170105 MGI 1620829 Zfp593 zinc finger protein 593 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220519 MGI 1620829 Zfp593 zinc finger protein 593 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1620829 Zfp593 zinc finger protein 593 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1620829 Zfp593 zinc finger protein 593 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1620829 Zfp593 zinc finger protein 593 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20220519 MGI 1620829 Zfp593 zinc finger protein 593 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210520 MGI 1620829 Zfp593 zinc finger protein 593 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20240523 MGI 1620829 Zfp593 zinc finger protein 593 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210520 MGI 1620829 Zfp593 zinc finger protein 593 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 1620830 H2bc4 H2B clustered histone 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1620830 H2bc4 H2B clustered histone 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 1620830 H2bc4 H2B clustered histone 4 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20201022 MGI 1620830 H2bc4 H2B clustered histone 4 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20201022 MGI 1620831 Coa8 cytochrome c oxidase assembly factor 8 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190912 MGI PMID:30552096 1620831 Coa8 cytochrome c oxidase assembly factor 8 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190912 MGI PMID:30552096 1620831 Coa8 cytochrome c oxidase assembly factor 8 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20190912 MGI PMID:30552096 1620831 Coa8 cytochrome c oxidase assembly factor 8 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20190912 MGI PMID:30552096 1620831 Coa8 cytochrome c oxidase assembly factor 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1620831 Coa8 cytochrome c oxidase assembly factor 8 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230119 MGI 1620831 Coa8 cytochrome c oxidase assembly factor 8 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20190912 MGI PMID:30552096 1620833 Zwilch zwilch kinetochore protein gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200310 MGI 1620833 Zwilch zwilch kinetochore protein gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20200310 MGI 1620833 Zwilch zwilch kinetochore protein gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20200310 MGI 1620833 Zwilch zwilch kinetochore protein gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1620833 Zwilch zwilch kinetochore protein gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20211021 MGI 1620833 Zwilch zwilch kinetochore protein gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20200310 MGI 1620833 Zwilch zwilch kinetochore protein gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1620833 Zwilch zwilch kinetochore protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620836 Ube2w ubiquitin-conjugating enzyme E2W (putative) gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20170601 MGI PMID:26601958 1620836 Ube2w ubiquitin-conjugating enzyme E2W (putative) gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20170601 MGI PMID:26601958 1620836 Ube2w ubiquitin-conjugating enzyme E2W (putative) gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20170601 MGI PMID:26601958 1620836 Ube2w ubiquitin-conjugating enzyme E2W (putative) gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20170601 MGI PMID:26601958 1620836 Ube2w ubiquitin-conjugating enzyme E2W (putative) gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20170601 MGI PMID:26601958 1620836 Ube2w ubiquitin-conjugating enzyme E2W (putative) gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1620836 Ube2w ubiquitin-conjugating enzyme E2W (putative) gene MP:0005159 azoospermia IAGP N RGD:5509061 20170601 MGI PMID:26601958 1620836 Ube2w ubiquitin-conjugating enzyme E2W (putative) gene MP:0009605 decreased keratohyalin granule number IAGP N RGD:5509061 20170601 MGI PMID:26601958 1620836 Ube2w ubiquitin-conjugating enzyme E2W (putative) gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1620836 Ube2w ubiquitin-conjugating enzyme E2W (putative) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170601 MGI PMID:26601958 1620836 Ube2w ubiquitin-conjugating enzyme E2W (putative) gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20170601 MGI PMID:26601958 1620836 Ube2w ubiquitin-conjugating enzyme E2W (putative) gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170601 MGI PMID:26601958 1620836 Ube2w ubiquitin-conjugating enzyme E2W (putative) gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1620837 4933436I01Rik RIKEN cDNA 4933436I01 gene gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201224 MGI PMID:32493902 1620839 Asb17 ankyrin repeat and SOCS box-containing 17 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220721 MGI PMID:35070814 1620839 Asb17 ankyrin repeat and SOCS box-containing 17 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20220721 MGI PMID:35070814 1620839 Asb17 ankyrin repeat and SOCS box-containing 17 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220721 MGI PMID:35070814 1620839 Asb17 ankyrin repeat and SOCS box-containing 17 gene MP:0031389 abnormal ectoplasmic specialization morphology IAGP N RGD:5509061 20220721 MGI PMID:35070814 1620841 4933411K16Rik RIKEN cDNA 4933411K16 gene gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1620842 Erich2 glutamate rich 2 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210708 MGI PMID:32561905 1620843 Rnf220 ring finger protein 220 gene MP:0000753 paralysis IAGP N RGD:5509061 20201001 MGI PMID:31291587 1620843 Rnf220 ring finger protein 220 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20200402 MGI PMID:30177510 1620843 Rnf220 ring finger protein 220 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20201002 MGI PMID:31291587 1620843 Rnf220 ring finger protein 220 gene MP:0002083 premature death IAGP N RGD:5509061 20201001 MGI PMID:31291587 1620843 Rnf220 ring finger protein 220 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20201002 MGI PMID:31291587 1620843 Rnf220 ring finger protein 220 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220811 MGI 1620843 Rnf220 ring finger protein 220 gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20201001 MGI PMID:31291587 1620843 Rnf220 ring finger protein 220 gene MP:0005390 skeleton phenotype IAGP N RGD:5509061 20201002 MGI PMID:31291587 1620843 Rnf220 ring finger protein 220 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20201002 MGI PMID:31291587 1620843 Rnf220 ring finger protein 220 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1620843 Rnf220 ring finger protein 220 gene MP:0021101 abnormal ventral interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:30177510 1620843 Rnf220 ring finger protein 220 gene MP:0021102 abnormal ventral interneuron 0 morphology IAGP N RGD:5509061 20220310 MGI PMID:30177510 1620843 Rnf220 ring finger protein 220 gene MP:0021103 abnormal ventral interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:30177510 1620843 Rnf220 ring finger protein 220 gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:30177510 1620843 Rnf220 ring finger protein 220 gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:30177510 1620846 Tab3 TGF-beta activated kinase 1/MAP3K7 binding protein 3 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23509369 1620846 Tab3 TGF-beta activated kinase 1/MAP3K7 binding protein 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1620846 Tab3 TGF-beta activated kinase 1/MAP3K7 binding protein 3 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23509369 1620846 Tab3 TGF-beta activated kinase 1/MAP3K7 binding protein 3 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:23509369 1620846 Tab3 TGF-beta activated kinase 1/MAP3K7 binding protein 3 gene MP:0002491 decreased IgD level IAGP N RGD:5509061 20141003 MGI PMID:23509369 1620846 Tab3 TGF-beta activated kinase 1/MAP3K7 binding protein 3 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:23509369 1620846 Tab3 TGF-beta activated kinase 1/MAP3K7 binding protein 3 gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:23509369 1620846 Tab3 TGF-beta activated kinase 1/MAP3K7 binding protein 3 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23509369 1620846 Tab3 TGF-beta activated kinase 1/MAP3K7 binding protein 3 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:23509369 1620846 Tab3 TGF-beta activated kinase 1/MAP3K7 binding protein 3 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:23509369 1620846 Tab3 TGF-beta activated kinase 1/MAP3K7 binding protein 3 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:23509369 1620846 Tab3 TGF-beta activated kinase 1/MAP3K7 binding protein 3 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:23509369 1620846 Tab3 TGF-beta activated kinase 1/MAP3K7 binding protein 3 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23509369 1620847 Spag16 sperm associated antigen 16 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:15328412 1620847 Spag16 sperm associated antigen 16 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:16382026 1620847 Spag16 sperm associated antigen 16 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:15328412 1620847 Spag16 sperm associated antigen 16 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:15328412 1620847 Spag16 sperm associated antigen 16 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:15328412 1620847 Spag16 sperm associated antigen 16 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:16382026 1620847 Spag16 sperm associated antigen 16 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:15328412 1620847 Spag16 sperm associated antigen 16 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:16382026 1620847 Spag16 sperm associated antigen 16 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:15328412 1620847 Spag16 sperm associated antigen 16 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20200310 MGI PMID:15328412 1620847 Spag16 sperm associated antigen 16 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200310 MGI PMID:16382026 1620847 Spag16 sperm associated antigen 16 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200310 MGI PMID:15328412 1620847 Spag16 sperm associated antigen 16 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15328412 1620847 Spag16 sperm associated antigen 16 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20200310 MGI PMID:16382026 1620847 Spag16 sperm associated antigen 16 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20200310 MGI PMID:15328412 1620847 Spag16 sperm associated antigen 16 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20200310 MGI PMID:15328412 1620847 Spag16 sperm associated antigen 16 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:15328412 1620847 Spag16 sperm associated antigen 16 gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20220811 MGI PMID:15328412 1620847 Spag16 sperm associated antigen 16 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220811 MGI PMID:15328412 1620849 Spesp1 sperm equatorial segment protein 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:20375058 1620849 Spesp1 sperm equatorial segment protein 1 gene MP:0005411 delayed fertilization IAGP N RGD:5509061 20141003 MGI PMID:20375058 1620849 Spesp1 sperm equatorial segment protein 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:20375058 1620849 Spesp1 sperm equatorial segment protein 1 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:20375058 1620851 Rbm4b RNA binding motif protein 4B gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1620851 Rbm4b RNA binding motif protein 4B gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:23129807 1620851 Rbm4b RNA binding motif protein 4B gene MP:0001759 increased urine glucose level IEA N RGD:5509061 20240523 MGI 1620851 Rbm4b RNA binding motif protein 4B gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1620851 Rbm4b RNA binding motif protein 4B gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23129807 1620851 Rbm4b RNA binding motif protein 4B gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1620851 Rbm4b RNA binding motif protein 4B gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:23129807 1620851 Rbm4b RNA binding motif protein 4B gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20181227 MGI 1620853 Myot myotilin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:17074808 1620855 Tmem59 transmembrane protein 59 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20180614 MGI PMID:28058580 1620855 Tmem59 transmembrane protein 59 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20180614 MGI PMID:28058580 1620855 Tmem59 transmembrane protein 59 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20180614 MGI PMID:28058580 1620855 Tmem59 transmembrane protein 59 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20180614 MGI PMID:28058580 1620855 Tmem59 transmembrane protein 59 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20180614 MGI PMID:28058580 1620855 Tmem59 transmembrane protein 59 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20180614 MGI PMID:28058580 1620855 Tmem59 transmembrane protein 59 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20180614 MGI PMID:28058580 1620855 Tmem59 transmembrane protein 59 gene MP:0020340 abnormal inhibitory learning IAGP N RGD:5509061 20180614 MGI PMID:28058580 1620855 Tmem59 transmembrane protein 59 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20180614 MGI PMID:28058580 1620855 Tmem59 transmembrane protein 59 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20180614 MGI PMID:28058580 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:17000766 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:17719010 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:17000766 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17719010 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:17719010 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:17000766 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:17719010 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17719010 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17719010 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:17000766 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17719010 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:17000766 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:17000766 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17719010 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:17000766 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:17000766 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:17000766 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:17719010 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20170309 MGI PMID:17000766 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0010811 decreased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:17000766 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0010887 pale lung IAGP N RGD:5509061 20141003 MGI PMID:17000766 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17000766 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17719010 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0011089 perinatal lethality, complete penetrance IMP N RGD:5688081|PMID:17719010 20120217 RGD 1620858 Ptges3 prostaglandin E synthase 3 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:17719010 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0002861 abnormal tail bud morphology IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0003794 delayed somite formation IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0009656 delayed chorioallantoic fusion IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620859 Tmed2 transmembrane p24 trafficking protein 2 gene MP:0012062 small tail bud IAGP N RGD:5509061 20200310 MGI PMID:20178780 1620860 Dnajb5 DnaJ heat shock protein family (Hsp40) member B5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1620861 Gps2 G protein pathway suppressor 2 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20160310 MGI PMID:25519902 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0000601 small liver IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200514 MGI 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0001147 small testis IEA N RGD:5509061 20200514 MGI 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0002188 small heart IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0003068 enlarged kidney IEA N RGD:5509061 20200514 MGI 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0011011 impaired lung lobe morphogenesis IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620862 Sinhcaf SIN3-HDAC complex associated factor gene MP:0012252 abnormal septum transversum morphology IAGP N RGD:5509061 20220721 MGI PMID:30070635 1620866 Vwa7 von Willebrand factor A domain containing 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1620867 Lsm2 LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 1620867 Lsm2 LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241010 MGI 1620867 Lsm2 LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1620867 Lsm2 LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1620868 Zfp146 zinc finger protein 146 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20230601 MGI 1620868 Zfp146 zinc finger protein 146 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1620872 Hax1 HCLS1 associated X-1 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0001428 adipsia IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18288109 1620872 Hax1 HCLS1 associated X-1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620872 Hax1 HCLS1 associated X-1 gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:20865787 1620873 Gpr34 G protein-coupled receptor 34 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21097509 1620873 Gpr34 G protein-coupled receptor 34 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20181227 MGI 1620873 Gpr34 G protein-coupled receptor 34 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:21097509 1620873 Gpr34 G protein-coupled receptor 34 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:21097509 1620873 Gpr34 G protein-coupled receptor 34 gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:21097509 1620873 Gpr34 G protein-coupled receptor 34 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21097509 1620873 Gpr34 G protein-coupled receptor 34 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:21097509 1620873 Gpr34 G protein-coupled receptor 34 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21097509 1620873 Gpr34 G protein-coupled receptor 34 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:21097509 1620873 Gpr34 G protein-coupled receptor 34 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21097509 1620873 Gpr34 G protein-coupled receptor 34 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:21097509 1620873 Gpr34 G protein-coupled receptor 34 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:21097509 1620873 Gpr34 G protein-coupled receptor 34 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:21097509 1620873 Gpr34 G protein-coupled receptor 34 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:21097509 1620873 Gpr34 G protein-coupled receptor 34 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:21097509 1620874 Gpc6 glypican 6 gene MP:0000111 cleft palate IAGP N RGD:5509061 20171221 MGI PMID:28696225 1620874 Gpc6 glypican 6 gene MP:0002764 short tibia IAGP N RGD:5509061 20171221 MGI PMID:28696225 1620874 Gpc6 glypican 6 gene MP:0002765 short fibula IAGP N RGD:5509061 20171221 MGI PMID:28696225 1620874 Gpc6 glypican 6 gene MP:0003109 short femur IAGP N RGD:5509061 20171221 MGI PMID:28696225 1620874 Gpc6 glypican 6 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20171221 MGI PMID:28696225 1620874 Gpc6 glypican 6 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20171221 MGI PMID:28696225 1620874 Gpc6 glypican 6 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20171221 MGI PMID:28696225 1620874 Gpc6 glypican 6 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20171221 MGI PMID:28696225 1620874 Gpc6 glypican 6 gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20171221 MGI PMID:28696225 1620874 Gpc6 glypican 6 gene MP:0005352 small cranium IAGP N RGD:5509061 20171221 MGI PMID:28696225 1620874 Gpc6 glypican 6 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20171221 MGI PMID:28696225 1620874 Gpc6 glypican 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20171221 MGI PMID:28696225 1620874 Gpc6 glypican 6 gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:28696225 1620874 Gpc6 glypican 6 gene MP:0030190 small snout IAGP N RGD:5509061 20171221 MGI PMID:28696225 1620875 Dand5 DAN domain family member 5, BMP antagonist gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15466485 1620875 Dand5 DAN domain family member 5, BMP antagonist gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15466485 1620875 Dand5 DAN domain family member 5, BMP antagonist gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:15466485 1620875 Dand5 DAN domain family member 5, BMP antagonist gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:15466485 1620875 Dand5 DAN domain family member 5, BMP antagonist gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:15466485 1620875 Dand5 DAN domain family member 5, BMP antagonist gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15466485 1620875 Dand5 DAN domain family member 5, BMP antagonist gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:15466485 1620875 Dand5 DAN domain family member 5, BMP antagonist gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15466485 1620878 Pappa2 pappalysin 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:23457539 1620878 Pappa2 pappalysin 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:23457539 1620878 Pappa2 pappalysin 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:23457539 1620878 Pappa2 pappalysin 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:21586553 1620878 Pappa2 pappalysin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21586553 1620878 Pappa2 pappalysin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23457539 1620878 Pappa2 pappalysin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23457539 1620878 Pappa2 pappalysin 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21586553 1620878 Pappa2 pappalysin 2 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:21586553 1620878 Pappa2 pappalysin 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:23457539 1620878 Pappa2 pappalysin 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21586553 1620878 Pappa2 pappalysin 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:21586553 1620878 Pappa2 pappalysin 2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:23457539 1620878 Pappa2 pappalysin 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:23457539 1620878 Pappa2 pappalysin 2 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:23457539 1620878 Pappa2 pappalysin 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:23457539 1620878 Pappa2 pappalysin 2 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23457539 1620878 Pappa2 pappalysin 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21586553 1620878 Pappa2 pappalysin 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:23457539 1620878 Pappa2 pappalysin 2 gene MP:0010114 abnormal coccyx morphology IAGP N RGD:5509061 20141003 MGI PMID:23457539 1620878 Pappa2 pappalysin 2 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20170907 MGI PMID:23457539 1620879 Clec5a C-type lectin domain family 5, member a gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1620879 Clec5a C-type lectin domain family 5, member a gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1620879 Clec5a C-type lectin domain family 5, member a gene MP:0001258 decreased body length IEA N RGD:5509061 20230601 MGI 1620879 Clec5a C-type lectin domain family 5, member a gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230601 MGI 1620879 Clec5a C-type lectin domain family 5, member a gene MP:0001314 cornea opacity IEA N RGD:5509061 20230601 MGI 1620879 Clec5a C-type lectin domain family 5, member a gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20212065 1620879 Clec5a C-type lectin domain family 5, member a gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20230601 MGI 1620880 Bves blood vessel epicardial substance gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1620880 Bves blood vessel epicardial substance gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20191128 MGI 1620880 Bves blood vessel epicardial substance gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1620880 Bves blood vessel epicardial substance gene MP:0003402 decreased liver weight IEA N RGD:5509061 20220519 MGI 1620880 Bves blood vessel epicardial substance gene MP:0004115 abnormal sinoatrial node morphology IAGP N RGD:5509061 20141003 MGI PMID:22354168 1620880 Bves blood vessel epicardial substance gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:22354168 1620880 Bves blood vessel epicardial substance gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20160114 MGI 1620880 Bves blood vessel epicardial substance gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:22354168 1620880 Bves blood vessel epicardial substance gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20211021 MGI 1620880 Bves blood vessel epicardial substance gene MP:0010052 increased grip strength IEA N RGD:5509061 20160114 MGI 1620880 Bves blood vessel epicardial substance gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 1620880 Bves blood vessel epicardial substance gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20141003 MGI PMID:22354168 1620880 Bves blood vessel epicardial substance gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1620880 Bves blood vessel epicardial substance gene MP:0031328 delayed skeletal muscle regeneration IAGP N RGD:5509061 20220106 MGI PMID:11839816 1620881 Slx Sycp3 like X-linked gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20210819 MGI PMID:31630956 1620881 Slx Sycp3 like X-linked gene MP:0001925 male infertility IAGP N RGD:5509061 20210819 MGI PMID:31630956 1620881 Slx Sycp3 like X-linked gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210819 MGI PMID:31630956 1620881 Slx Sycp3 like X-linked gene MP:0002686 globozoospermia IAGP N RGD:5509061 20210819 MGI PMID:31630956 1620881 Slx Sycp3 like X-linked gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210819 MGI PMID:31630956 1620881 Slx Sycp3 like X-linked gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210819 MGI PMID:31630956 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0000745 tremors IAGP N RGD:5509061 20200310 MGI PMID:11003697 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:11003697 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20200310 MGI PMID:11984826 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20200310 MGI PMID:11984826 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:11003697 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:10906391 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0002495 increased IgA level IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0002497 increased IgE level IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0002816 colitis IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0002822 catalepsy IAGP N RGD:5509061 20200310 MGI PMID:11003697 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20200310 MGI PMID:21881209 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0004611 increased susceptibility to ototoxicity-induced hearing loss IAGP N RGD:5509061 20200310 MGI PMID:10661503 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0004999 abnormal blood-inner ear barrier function IAGP N RGD:5509061 20200310 MGI PMID:10661503 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20200310 MGI PMID:11003697 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0005037 mucous diarrhea IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20200310 MGI PMID:10906391 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0005150 cachexia IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20200310 MGI PMID:11003697 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20200310 MGI PMID:10906391 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008401 abnormal CD8 positive, alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20200310 MGI PMID:10906391 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:10906391 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20200310 MGI PMID:10906391 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:10661503 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:11003697 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:7910522 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200310 MGI PMID:9144452 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20200310 MGI PMID:10661503 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20200310 MGI PMID:10906391 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20200310 MGI PMID:16611851 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20200310 MGI PMID:9108099 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:11984826 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0013803 increased IgG2 level IAGP N RGD:5509061 20200310 MGI PMID:9820555 1620890 Abcb1a ATP-binding cassette, sub-family B member 1A gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:7910522 1620892 Pfdn2 prefoldin 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1620892 Pfdn2 prefoldin 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20141003 MGI 1620892 Pfdn2 prefoldin 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1620894 Marcksl1 MARCKS-like 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:8700893 1620894 Marcksl1 MARCKS-like 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:8700893 1620894 Marcksl1 MARCKS-like 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200310 MGI PMID:8700893 1620894 Marcksl1 MARCKS-like 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200310 MGI PMID:8700893 1620894 Marcksl1 MARCKS-like 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20200310 MGI PMID:8700893 1620894 Marcksl1 MARCKS-like 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:8700893 1620894 Marcksl1 MARCKS-like 1 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20200310 MGI PMID:8700893 1620894 Marcksl1 MARCKS-like 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20200310 MGI PMID:8700893 1620894 Marcksl1 MARCKS-like 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:9837946 1620894 Marcksl1 MARCKS-like 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20200310 MGI PMID:8700893 1620894 Marcksl1 MARCKS-like 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20200310 MGI PMID:8700893 1620894 Marcksl1 MARCKS-like 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:8700893 1620894 Marcksl1 MARCKS-like 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20200310 MGI PMID:8700893 1620894 Marcksl1 MARCKS-like 1 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200310 MGI PMID:8700893 1620895 Afdn afadin, adherens junction formation factor gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200514 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210520 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210520 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0000599 enlarged liver IEA N RGD:5509061 20210520 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0000692 small spleen IEA N RGD:5509061 20201022 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 1620895 Afdn afadin, adherens junction formation factor gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 1620895 Afdn afadin, adherens junction formation factor gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20150101 MGI PMID:25100583 1620895 Afdn afadin, adherens junction formation factor gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 1620895 Afdn afadin, adherens junction formation factor gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:10469590 1620895 Afdn afadin, adherens junction formation factor gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20150101 MGI PMID:25100583 1620895 Afdn afadin, adherens junction formation factor gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20201022 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:10469590 1620895 Afdn afadin, adherens junction formation factor gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:10469590 1620895 Afdn afadin, adherens junction formation factor gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:10477764 1620895 Afdn afadin, adherens junction formation factor gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:10469590 1620895 Afdn afadin, adherens junction formation factor gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:10477764 1620895 Afdn afadin, adherens junction formation factor gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:10477764 1620895 Afdn afadin, adherens junction formation factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10469590 1620895 Afdn afadin, adherens junction formation factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10477764 1620895 Afdn afadin, adherens junction formation factor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10469590 1620895 Afdn afadin, adherens junction formation factor gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10477764 1620895 Afdn afadin, adherens junction formation factor gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:22219273 1620895 Afdn afadin, adherens junction formation factor gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20150101 MGI PMID:25100583 1620895 Afdn afadin, adherens junction formation factor gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:10469590 1620895 Afdn afadin, adherens junction formation factor gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:10477764 1620895 Afdn afadin, adherens junction formation factor gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 1620895 Afdn afadin, adherens junction formation factor gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20200514 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:10469590 1620895 Afdn afadin, adherens junction formation factor gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10469590 1620895 Afdn afadin, adherens junction formation factor gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 1620895 Afdn afadin, adherens junction formation factor gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20211021 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20150101 MGI PMID:25100583 1620895 Afdn afadin, adherens junction formation factor gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20210520 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0005238 increased brain size IAGP N RGD:5509061 20150101 MGI PMID:25100583 1620895 Afdn afadin, adherens junction formation factor gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20200514 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:10469590 1620895 Afdn afadin, adherens junction formation factor gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:22219273 1620895 Afdn afadin, adherens junction formation factor gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20150101 MGI PMID:25100583 1620895 Afdn afadin, adherens junction formation factor gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 1620895 Afdn afadin, adherens junction formation factor gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 1620895 Afdn afadin, adherens junction formation factor gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:19481057 1620895 Afdn afadin, adherens junction formation factor gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:22219273 1620895 Afdn afadin, adherens junction formation factor gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22219273 1620895 Afdn afadin, adherens junction formation factor gene MP:0010011 ectopic hippocampus pyramidal cells IAGP N RGD:5509061 20141003 MGI PMID:22219273 1620895 Afdn afadin, adherens junction formation factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10469590 1620895 Afdn afadin, adherens junction formation factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10477764 1620895 Afdn afadin, adherens junction formation factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:10477764 1620895 Afdn afadin, adherens junction formation factor gene MP:0011200 abnormal extraembryonic coelom morphology IAGP N RGD:5509061 20141003 MGI PMID:10477764 1620895 Afdn afadin, adherens junction formation factor gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:10477764 1620895 Afdn afadin, adherens junction formation factor gene MP:0011625 cystolithiasis IEA N RGD:5509061 20210520 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20150101 MGI PMID:25100583 1620895 Afdn afadin, adherens junction formation factor gene MP:0012165 absent neural folds IAGP N RGD:5509061 20141003 MGI PMID:10469590 1620895 Afdn afadin, adherens junction formation factor gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1620895 Afdn afadin, adherens junction formation factor gene MP:0020067 increased neocortex size IAGP N RGD:5509061 20150101 MGI PMID:25100583 1620895 Afdn afadin, adherens junction formation factor gene MP:0020389 increased radial glial cell number IAGP N RGD:5509061 20161117 MGI PMID:25100583 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10887138 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12629167 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12629167 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:12629167 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10887138 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12629167 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:12629167 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:10932191 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12629167 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:12629167 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10887138 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12629167 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12629167 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12629167 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10887138 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:12629167 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12629167 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:10887138 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:12629167 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10887138 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10887138 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:12629167 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10887138 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10887138 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10887138 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10887138 1620896 Aff1 AF4/FMR2 family, member 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12629167 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210128 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20220811 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20220519 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210826 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20180315 MGI PMID:25464900 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0008797 facial cleft IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20210520 MGI 1620897 Mllt10 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000060 delayed bone ossification IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000074 abnormal neurocranium morphology IEA N RGD:5509061 20171109 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000075 absent neurocranium IAGP N RGD:5509061 20171102 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0000088 short mandible IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000104 abnormal sphenoid bone morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0000149 abnormal scapula morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0000158 absent sternum IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0000163 abnormal cartilage morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000164 abnormal cartilage development IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0000445 short snout IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:10704385 1620902 Foxc1 forkhead box C1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:10704385 1620902 Foxc1 forkhead box C1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:10704385 1620902 Foxc1 forkhead box C1 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0000547 short limbs IAGP N RGD:5509061 20160114 MGI PMID:25808752 1620902 Foxc1 forkhead box C1 gene MP:0000554 abnormal carpal bone morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:19879845 1620902 Foxc1 forkhead box C1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15314648 1620902 Foxc1 forkhead box C1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19879845 1620902 Foxc1 forkhead box C1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:19879845 1620902 Foxc1 forkhead box C1 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0000820 abnormal choroid plexus morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000823 abnormal lateral ventricle morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000825 dilated lateral ventricle IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000826 abnormal third ventricle morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000828 abnormal fourth ventricle morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0000923 abnormal roof plate morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0001092 abnormal trigeminal ganglion morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0001127 small ovary IAGP N RGD:5509061 20150312 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20150212 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:10395790 1620902 Foxc1 forkhead box C1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0001346 abnormal lacrimal gland morphology IAGP N RGD:5509061 20150212 MGI PMID:16470615 1620902 Foxc1 forkhead box C1 gene MP:0001348 abnormal lacrimal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:16470615 1620902 Foxc1 forkhead box C1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:15196959 1620902 Foxc1 forkhead box C1 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:15196959 1620902 Foxc1 forkhead box C1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:22522965 1620902 Foxc1 forkhead box C1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0001893 non-obstructive hydrocephaly IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0001953 respiratory failure IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:22522965 1620902 Foxc1 forkhead box C1 gene MP:0002113 abnormal skeleton development IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0002114 abnormal axial skeleton morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0002115 abnormal limb bone morphology IEA N RGD:5509061 20111222 MGI 1620902 Foxc1 forkhead box C1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22522965 1620902 Foxc1 forkhead box C1 gene MP:0002187 abnormal fibula morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0002200 abnormal brain ventricular system morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0002256 abnormal laryngeal cartilage morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0002257 abnormal arytenoid cartilage morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0002258 abnormal cricoid cartilage morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0002748 abnormal pulmonary valve morphology IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0002823 abnormal rib development IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0002825 abnormal notochord morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20141003 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0003048 abnormal cervical vertebrae morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0003056 abnormal hyoid bone morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0003072 abnormal metatarsal bone morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0003073 abnormal metacarpal bone morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:18187037 1620902 Foxc1 forkhead box C1 gene MP:0003120 abnormal tracheal cartilage morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20160114 MGI PMID:25808752 1620902 Foxc1 forkhead box C1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20160114 MGI PMID:25808752 1620902 Foxc1 forkhead box C1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10704385 1620902 Foxc1 forkhead box C1 gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20141003 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0003584 bifid ureter IAGP N RGD:5509061 20141003 MGI PMID:10704385 1620902 Foxc1 forkhead box C1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0003816 abnormal pituitary gland development IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0003817 abnormal pituitary diverticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:10704385 1620902 Foxc1 forkhead box C1 gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0003935 abnormal craniofacial development IEA N RGD:5509061 20171221 MGI 1620902 Foxc1 forkhead box C1 gene MP:0004017 duplex kidney IAGP N RGD:5509061 20141003 MGI PMID:10704385 1620902 Foxc1 forkhead box C1 gene MP:0004017 duplex kidney IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0004077 abnormal striatum morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0004085 abnormal heartbeat IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20160114 MGI PMID:25808752 1620902 Foxc1 forkhead box C1 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0004222 iris synechia IAGP N RGD:5509061 20141003 MGI PMID:12624268 1620902 Foxc1 forkhead box C1 gene MP:0004223 hypoplastic trabecular meshwork IAGP N RGD:5509061 20141003 MGI PMID:12624268 1620902 Foxc1 forkhead box C1 gene MP:0004226 absent Schlemm's canal IAGP N RGD:5509061 20141003 MGI PMID:12624268 1620902 Foxc1 forkhead box C1 gene MP:0004226 absent Schlemm's canal IAGP N RGD:5509061 20160414 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0004322 abnormal sternebra morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0004351 short humerus IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0004355 short radius IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0004359 short ulna IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0004376 absent frontal bone IEA N RGD:5509061 20171102 MGI 1620902 Foxc1 forkhead box C1 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0004600 abnormal vertebral transverse process morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0004670 small vertebral body IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0004674 thin ribs IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0004726 abnormal nasal capsule morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0004915 abnormal Reichert's cartilage morphology IEA N RGD:5509061 20111229 MGI 1620902 Foxc1 forkhead box C1 gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0005198 abnormal aqueous drainage system morphology IAGP N RGD:5509061 20141003 MGI PMID:12624268 1620902 Foxc1 forkhead box C1 gene MP:0005199 abnormal iris pigment epithelium IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0005203 abnormal trabecular meshwork morphology IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0005203 abnormal trabecular meshwork morphology IAGP N RGD:5509061 20141003 MGI PMID:12624268 1620902 Foxc1 forkhead box C1 gene MP:0005204 abnormal canal of Schlemm morphology IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20160114 MGI PMID:25808752 1620902 Foxc1 forkhead box C1 gene MP:0005269 abnormal occipital bone morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10395790 1620902 Foxc1 forkhead box C1 gene MP:0005306 abnormal phalanx morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0005353 abnormal patella morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0005537 abnormal cerebral aqueduct morphology IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0005623 abnormal meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10395790 1620902 Foxc1 forkhead box C1 gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0006064 abnormal superior vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20150430 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0006230 iris stroma hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0006241 abnormal placement of pupils IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0006250 abnormal line of Schwalbe morphology IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:15196959 1620902 Foxc1 forkhead box C1 gene MP:0006419 disorganized testis cords IAGP N RGD:5509061 20150416 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20160114 MGI PMID:25808752 1620902 Foxc1 forkhead box C1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0008275 failure of endochondral bone ossification IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0008276 failure of intramembranous bone ossification IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20150205 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0008278 failure of sternum ossification IAGP N RGD:5509061 20160114 MGI PMID:25808752 1620902 Foxc1 forkhead box C1 gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20141003 MGI PMID:10704385 1620902 Foxc1 forkhead box C1 gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20141003 MGI PMID:15196959 1620902 Foxc1 forkhead box C1 gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20141003 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0008915 fused carpal bones IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0008919 fused tarsal bones IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0008969 abnormal nasolacrimal duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16470615 1620902 Foxc1 forkhead box C1 gene MP:0009003 abnormal vibrissa number IEA N RGD:5509061 20111116 MGI 1620902 Foxc1 forkhead box C1 gene MP:0009022 abnormal brain meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:19879845 1620902 Foxc1 forkhead box C1 gene MP:0009071 short oviduct IAGP N RGD:5509061 20141003 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20141003 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0009825 cornea ulcer IAGP N RGD:5509061 20150430 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19879845 1620902 Foxc1 forkhead box C1 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:19879845 1620902 Foxc1 forkhead box C1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0010502 ventricle myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0010526 aortic arch coarctation IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0010595 abnormal aortic valve cusp morphology IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0010602 abnormal pulmonary valve cusp morphology IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0010605 thick pulmonary valve cusps IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0010709 absent eye anterior chamber IAGP N RGD:5509061 20141003 MGI PMID:22522965 1620902 Foxc1 forkhead box C1 gene MP:0010709 absent eye anterior chamber IAGP N RGD:5509061 20160310 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0010941 abnormal foramen magnum morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0010980 ectopic ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:10704385 1620902 Foxc1 forkhead box C1 gene MP:0010981 abnormal branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10704385 1620902 Foxc1 forkhead box C1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0011309 abnormal kidney arterial blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0011311 abnormal kidney venous blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0011318 abnormal right renal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0011364 abnormal metanephros morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0011410 ectopic testis IAGP N RGD:5509061 20141003 MGI PMID:10704385 1620902 Foxc1 forkhead box C1 gene MP:0011410 ectopic testis IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20141003 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0011486 ectopic ureter IAGP N RGD:5509061 20141003 MGI PMID:10704385 1620902 Foxc1 forkhead box C1 gene MP:0011493 double ureter IAGP N RGD:5509061 20141003 MGI PMID:10704385 1620902 Foxc1 forkhead box C1 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:10479458 1620902 Foxc1 forkhead box C1 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20160310 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0011727 ectopic ovary IAGP N RGD:5509061 20141003 MGI PMID:10704385 1620902 Foxc1 forkhead box C1 gene MP:0011727 ectopic ovary IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0011797 blind ureter IAGP N RGD:5509061 20141003 MGI PMID:10704385 1620902 Foxc1 forkhead box C1 gene MP:0011835 abnormal urogenital fold morphology IAGP N RGD:5509061 20141003 MGI PMID:5500588 1620902 Foxc1 forkhead box C1 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:22522965 1620902 Foxc1 forkhead box C1 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20160310 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0012176 abnormal head development IAGP N RGD:5509061 20171214 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0012184 absent paraxial mesoderm IAGP N RGD:5509061 20141003 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0012513 absent sternum body IEA N RGD:5509061 20141003 MGI 1620902 Foxc1 forkhead box C1 gene MP:0013200 head mesenchyme hypoplasia IAGP N RGD:5509061 20171214 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0013261 absent epiglottis IEA N RGD:5509061 20141003 MGI 1620902 Foxc1 forkhead box C1 gene MP:0013440 abnormal exorbital lacrimal gland morphology IAGP N RGD:5509061 20150205 MGI PMID:16470615 1620902 Foxc1 forkhead box C1 gene MP:0013474 abnormal lacrimal gland branching morphogenesis IAGP N RGD:5509061 20150212 MGI PMID:16470615 1620902 Foxc1 forkhead box C1 gene MP:0013605 abnormal ovarian bursa morphology IAGP N RGD:5509061 20150312 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0013608 abnormal ovarian cortex morphology IAGP N RGD:5509061 20150312 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0013609 abnormal ovarian medulla morphology IAGP N RGD:5509061 20150312 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0013738 abnormal testis tunica albuginea morphology IAGP N RGD:5509061 20150416 MGI PMID:16412416 1620902 Foxc1 forkhead box C1 gene MP:0013743 ciliary body hypoplasia IAGP N RGD:5509061 20150416 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0014153 absent intraorbital lacrimal gland IAGP N RGD:5509061 20160407 MGI PMID:16470615 1620902 Foxc1 forkhead box C1 gene MP:0014164 abnormal ciliary process morphology IAGP N RGD:5509061 20160414 MGI PMID:10767326 1620902 Foxc1 forkhead box C1 gene MP:0020391 radial glial endfoot detachment IAGP N RGD:5509061 20161117 MGI PMID:17715063 1620902 Foxc1 forkhead box C1 gene MP:0020854 increased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:10395790 1620902 Foxc1 forkhead box C1 gene MP:0030026 small Meckel's cartilage IEA N RGD:5509061 20170810 MGI 1620902 Foxc1 forkhead box C1 gene MP:0030302 abnormal maxillary zygomatic process morphology IAGP N RGD:5509061 20171102 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0030318 enlarged maxillary zygomatic process IAGP N RGD:5509061 20171109 MGI PMID:9635428 1620902 Foxc1 forkhead box C1 gene MP:0030337 enlarged third pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:11562355 1620902 Foxc1 forkhead box C1 gene MP:0030420 short basicranium IEA N RGD:5509061 20171214 MGI 1620902 Foxc1 forkhead box C1 gene MP:0030859 absent sesamoid bone of gastrocnemius IEA N RGD:5509061 20181025 MGI 1620902 Foxc1 forkhead box C1 gene MP:0030861 abnormal triquetrum morphology IEA N RGD:5509061 20181101 MGI 1620905 Igh-8 immunoglobulin heavy chain 8 (heavy chain of IgG3) gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:11907102 1620905 Igh-8 immunoglobulin heavy chain 8 (heavy chain of IgG3) gene MP:0002493 increased IgG level IAGP N RGD:5509061 20111116 MGI PMID:11907102 1620905 Igh-8 immunoglobulin heavy chain 8 (heavy chain of IgG3) gene MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:11907102 1620905 Igh-8 immunoglobulin heavy chain 8 (heavy chain of IgG3) gene MP:0002494 increased IgM level IAGP N RGD:5509061 20111116 MGI PMID:9759856 1620905 Igh-8 immunoglobulin heavy chain 8 (heavy chain of IgG3) gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20111116 MGI PMID:16507599 1620905 Igh-8 immunoglobulin heavy chain 8 (heavy chain of IgG3) gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20111116 MGI PMID:18077389 1620905 Igh-8 immunoglobulin heavy chain 8 (heavy chain of IgG3) gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20111116 MGI PMID:21378751 1620905 Igh-8 immunoglobulin heavy chain 8 (heavy chain of IgG3) gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20111116 MGI PMID:18077389 1620906 Spsb2 splA/ryanodine receptor domain and SOCS box containing 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20200310 MGI PMID:15964819 1620906 Spsb2 splA/ryanodine receptor domain and SOCS box containing 2 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20200310 MGI PMID:15964819 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:12829789 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17620412 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0001260 increased body weight IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19174477 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220714 MGI PMID:18812566 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22923474 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12829789 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:12829789 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:17620412 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:22923474 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:12829789 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0003397 increased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:17620412 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22923474 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17620412 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19174477 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0004199 increased fetal size IAGP N RGD:5509061 20141003 MGI PMID:12829789 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:19174477 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:19174477 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0004260 enlarged placenta IAGP N RGD:5509061 20141003 MGI PMID:12829789 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:19174477 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22923474 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22923474 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22923474 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:17620412 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0006320 abnormal interscapular fat pad morphology IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:17620412 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:22923474 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:22923474 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0009119 increased brown fat cell size IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0009702 increased birth body size IAGP N RGD:5509061 20141003 MGI PMID:12829789 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:22923474 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:12829789 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12829789 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20220714 MGI PMID:18812566 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20220714 MGI PMID:18812566 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22923474 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20180111 MGI PMID:24746805 1620908 Grb10 growth factor receptor bound protein 10 gene MP:0020520 whitened brown adipose tissue morphology IAGP N RGD:5509061 20180208 MGI PMID:24746805 1620910 Lilrb4b leukocyte immunoglobulin-like receptor, subfamily B, member 4B gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 1620910 Lilrb4b leukocyte immunoglobulin-like receptor, subfamily B, member 4B gene MP:0010507 shortened RR interval IEA N RGD:5509061 20230601 MGI 1620911 Pdpn podoplanin gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 1620911 Pdpn podoplanin gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20200310 MGI PMID:18265012 1620911 Pdpn podoplanin gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20200310 MGI PMID:18265012 1620911 Pdpn podoplanin gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20200310 MGI PMID:18265012 1620911 Pdpn podoplanin gene MP:0000726 absent lymphocyte IAGP N RGD:5509061 20200310 MGI PMID:23995678 1620911 Pdpn podoplanin gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:12654292 1620911 Pdpn podoplanin gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:16869965 1620911 Pdpn podoplanin gene MP:0001177 atelectasis IAGP N RGD:5509061 20200310 MGI PMID:12654292 1620911 Pdpn podoplanin gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20200310 MGI PMID:12654292 1620911 Pdpn podoplanin gene MP:0001284 absent vibrissae IEA N RGD:5509061 20200310 MGI 1620911 Pdpn podoplanin gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:12654292 1620911 Pdpn podoplanin gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:23995678 1620911 Pdpn podoplanin gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:12853470 1620911 Pdpn podoplanin gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:20363774 1620911 Pdpn podoplanin gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:23995678 1620911 Pdpn podoplanin gene MP:0001953 respiratory failure IAGP N RGD:5509061 20200310 MGI PMID:12654292 1620911 Pdpn podoplanin gene MP:0001953 respiratory failure IAGP N RGD:5509061 20200310 MGI PMID:16738320 1620911 Pdpn podoplanin gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20200310 MGI PMID:18265012 1620911 Pdpn podoplanin gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20200310 MGI PMID:12654292 1620911 Pdpn podoplanin gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20200310 MGI PMID:16869965 1620911 Pdpn podoplanin gene MP:0002274 abnormal type I pneumocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:12654292 1620911 Pdpn podoplanin gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20200310 MGI PMID:23995678 1620911 Pdpn podoplanin gene MP:0002652 thin myocardium IAGP N RGD:5509061 20200310 MGI PMID:18265012 1620911 Pdpn podoplanin gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20200310 MGI PMID:23995678 1620911 Pdpn podoplanin gene MP:0003288 intestinal edema IAGP N RGD:5509061 20200310 MGI PMID:20363774 1620911 Pdpn podoplanin gene MP:0003390 lymphedema IAGP N RGD:5509061 20200310 MGI PMID:12853470 1620911 Pdpn podoplanin gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20200310 MGI PMID:12853470 1620911 Pdpn podoplanin gene MP:0004038 lymphangiectasis IAGP N RGD:5509061 20200310 MGI PMID:12853470 1620911 Pdpn podoplanin gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20200310 MGI PMID:18265012 1620911 Pdpn podoplanin gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20200310 MGI PMID:18265012 1620911 Pdpn podoplanin gene MP:0004197 abnormal fetal growth/weight/body size IAGP N RGD:5509061 20200310 MGI PMID:12654292 1620911 Pdpn podoplanin gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1620911 Pdpn podoplanin gene MP:0005202 lethargy IAGP N RGD:5509061 20200310 MGI PMID:12654292 1620911 Pdpn podoplanin gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20200310 MGI PMID:18265012 1620911 Pdpn podoplanin gene MP:0008464 absent peripheral lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:23995678 1620911 Pdpn podoplanin gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20200310 MGI PMID:27066737 1620911 Pdpn podoplanin gene MP:0009432 increased fetal weight IAGP N RGD:5509061 20200310 MGI PMID:16738320 1620911 Pdpn podoplanin gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20200310 MGI PMID:12853470 1620911 Pdpn podoplanin gene MP:0010426 abnormal heart and great artery attachment IAGP N RGD:5509061 20200310 MGI PMID:18265012 1620911 Pdpn podoplanin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:12654292 1620911 Pdpn podoplanin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16738320 1620911 Pdpn podoplanin gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18265012 1620911 Pdpn podoplanin gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18265012 1620911 Pdpn podoplanin gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:18265012 1620911 Pdpn podoplanin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1620911 Pdpn podoplanin gene MP:0031051 lymph node hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:23995678 1620911 Pdpn podoplanin gene MP:0031589 detached epicardium IAGP N RGD:5509061 20240229 MGI PMID:18265012 1620913 Gngt2 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210128 MGI 1620913 Gngt2 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210826 MGI 1620913 Gngt2 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 2 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20220811 MGI 1620913 Gngt2 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210520 MGI 1620913 Gngt2 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1620913 Gngt2 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 2 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20221215 MGI 1620913 Gngt2 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20221215 MGI 1620913 Gngt2 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1620913 Gngt2 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1620915 Gng3 guanine nucleotide binding protein (G protein), gamma 3 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:15314181 1620915 Gng3 guanine nucleotide binding protein (G protein), gamma 3 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:15314181 1620915 Gng3 guanine nucleotide binding protein (G protein), gamma 3 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:22207761 1620915 Gng3 guanine nucleotide binding protein (G protein), gamma 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15314181 1620915 Gng3 guanine nucleotide binding protein (G protein), gamma 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22207761 1620915 Gng3 guanine nucleotide binding protein (G protein), gamma 3 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:22207761 1620915 Gng3 guanine nucleotide binding protein (G protein), gamma 3 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:22207761 1620915 Gng3 guanine nucleotide binding protein (G protein), gamma 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15314181 1620915 Gng3 guanine nucleotide binding protein (G protein), gamma 3 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:15314181 1620915 Gng3 guanine nucleotide binding protein (G protein), gamma 3 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15314181 1620915 Gng3 guanine nucleotide binding protein (G protein), gamma 3 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15314181 1620915 Gng3 guanine nucleotide binding protein (G protein), gamma 3 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:22207761 1620917 Atn1 atrophin 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210520 MGI 1620917 Atn1 atrophin 1 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20231207 MGI 1620917 Atn1 atrophin 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200310 MGI 1620917 Atn1 atrophin 1 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:19681162 1620917 Atn1 atrophin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:19681162 1620917 Atn1 atrophin 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201022 MGI 1620917 Atn1 atrophin 1 gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 1620917 Atn1 atrophin 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20200310 MGI 1620917 Atn1 atrophin 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1620917 Atn1 atrophin 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20200310 MGI 1620917 Atn1 atrophin 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210520 MGI 1620917 Atn1 atrophin 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:19681162 1620917 Atn1 atrophin 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1620917 Atn1 atrophin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:19681162 1620917 Atn1 atrophin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:17150957 1620917 Atn1 atrophin 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200310 MGI PMID:19681162 1620917 Atn1 atrophin 1 gene MP:0002673 abnormal sperm number IAGP N RGD:5509061 20200310 MGI PMID:19681162 1620917 Atn1 atrophin 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1620917 Atn1 atrophin 1 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20211021 MGI 1620917 Atn1 atrophin 1 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20211021 MGI 1620917 Atn1 atrophin 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210520 MGI 1620917 Atn1 atrophin 1 gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20211021 MGI 1620917 Atn1 atrophin 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20200310 MGI 1620917 Atn1 atrophin 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1620917 Atn1 atrophin 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19681162 1620917 Atn1 atrophin 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20200310 MGI PMID:19681162 1620918 Drg2 developmentally regulated GTP binding protein 2 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20160804 MGI 1620918 Drg2 developmentally regulated GTP binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200806 MGI PMID:31861806 1620918 Drg2 developmentally regulated GTP binding protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200806 MGI PMID:31861806 1620918 Drg2 developmentally regulated GTP binding protein 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200806 MGI PMID:31861806 1620918 Drg2 developmentally regulated GTP binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200806 MGI PMID:31861806 1620918 Drg2 developmentally regulated GTP binding protein 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20200806 MGI PMID:26582392 1620918 Drg2 developmentally regulated GTP binding protein 2 gene MP:0003313 abnormal locomotor activation IEA N RGD:5509061 20141003 MGI 1620918 Drg2 developmentally regulated GTP binding protein 2 gene MP:0004357 long tibia IEA N RGD:5509061 20160804 MGI 1620918 Drg2 developmentally regulated GTP binding protein 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20200806 MGI PMID:31861806 1620918 Drg2 developmentally regulated GTP binding protein 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200806 MGI PMID:31861806 1620918 Drg2 developmentally regulated GTP binding protein 2 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20200806 MGI PMID:26582392 1620918 Drg2 developmentally regulated GTP binding protein 2 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20200806 MGI PMID:31861806 1620918 Drg2 developmentally regulated GTP binding protein 2 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20200806 MGI PMID:31861806 1620919 Dpagt1 dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:10536042 1620919 Dpagt1 dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20180719 MGI PMID:10536042 1620919 Dpagt1 dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:10536042 1620919 Dpagt1 dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:17477386 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0000947 convulsive seizures IEA N RGD:5509061 20201022 MGI 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:17477386 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17477386 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17477386 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17477386 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17477386 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17477386 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17477386 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10555141 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10555141 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15215868 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15215868 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15215868 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10555141 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15215868 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17477386 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20240627 MGI PMID:38627502 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20240627 MGI PMID:38627502 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0002400 abnormal multipotent stem cell morphology IAGP N RGD:5509061 20190418 MGI PMID:30692594 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20240627 MGI PMID:37527244 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:22056672 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20240627 MGI PMID:37527244 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20240627 MGI PMID:38627502 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20190418 MGI PMID:30692594 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15215868 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:15215868 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230601 MGI 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20240627 MGI PMID:38627502 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20240627 MGI PMID:38627502 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:10555141 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:17182866 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20240627 MGI PMID:37527244 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20240627 MGI PMID:38627502 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22056672 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:22056672 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0009203 external male genitalia hypoplasia IAGP N RGD:5509061 20240627 MGI PMID:38627502 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20190418 MGI PMID:30692594 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20240627 MGI PMID:37527244 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0010052 increased grip strength IEA N RGD:5509061 20150430 MGI 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:17477386 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17477386 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10555141 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240627 MGI PMID:37527244 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0013660 abnormal bone marrow hematopoietic cell morphology IAGP N RGD:5509061 20190418 MGI PMID:30692594 1620920 Dnmt3a DNA methyltransferase 3A gene MP:0013891 increased common myeloid progenitor cell number IAGP N RGD:5509061 20190418 MGI PMID:30692594 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12859898 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0000276 heart right ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0000286 abnormal mitral valve morphology IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0000477 abnormal intestine morphology IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:2612382 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0000542 left-sided isomerism IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:2612382 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:1638728 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:2612382 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:19235720 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0000650 mesocardia IAGP N RGD:5509061 20141003 MGI PMID:19235720 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:1638728 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0001293 anophthalmia IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0001297 microphthalmia IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10556073 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0001727 abnormal embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:1638728 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19235720 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:2612382 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12859898 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0001943 abnormal respiration IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20170223 MGI PMID:20511334 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:1638728 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12859898 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0002189 abnormal myocardial trabeculae morphology IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0002625 heart left ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0002639 micrognathia IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:10556073 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:12859898 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:1638728 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:19235720 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:2612382 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:1638728 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:10556073 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:19235720 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:2612382 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0003342 accessory spleen IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20170223 MGI PMID:20511334 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0003675 kidney cyst IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0004017 duplex kidney IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:10556073 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:12859898 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0004131 abnormal motile primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:10549278 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0004133 heterotaxia IEA N RGD:5509061 20111116 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20170223 MGI PMID:20511334 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0004158 right aortic arch IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0004391 abnormal respiratory conducting tube morphology IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0004703 abnormal vertebral column morphology IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0004733 abnormal thoracic cavity morphology IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0005083 abnormal biliary tract morphology IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:1638728 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0006063 abnormal inferior vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:1638728 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20170223 MGI PMID:20511334 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0008461 left atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:1638728 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:2612382 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0008933 abnormal motile primary cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:10556073 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0008933 abnormal motile primary cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:12859898 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20170223 MGI PMID:20511334 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20170223 MGI PMID:20511334 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20170223 MGI PMID:20511334 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0010460 pulmonary artery hypoplasia IAGP N RGD:5509061 20170223 MGI PMID:20511334 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0010466 vascular ring IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0010489 abnormal heart atrium auricular region morphology IAGP N RGD:5509061 20141003 MGI PMID:1638728 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0010607 common atrioventricular valve IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0010668 abnormal hepatic portal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:1638728 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0010807 abnormal stomach position or orientation IAGP N RGD:5509061 20141003 MGI PMID:19235720 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:10556073 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:19235720 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0010975 abnormal lung lobe morphology IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0011055 abnormal respiratory motile cilium physiology IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0011249 abdominal situs inversus IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0011250 abdominal situs ambiguus IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0011252 situs inversus totalis IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0011253 situs inversus with levocardia IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0011254 superior-inferior ventricles IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0011510 biventricular, discordant atrioventricular connection IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0011511 biventricular, ambiguous atrioventricular connection IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0011649 immotile respiratory cilia IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0011665 d-loop transposition of the great arteries IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0011666 double outlet right ventricle, ventricular defect committed to aorta IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0011745 isolation of the left subclavian artery IEA N RGD:5509061 20141003 MGI 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0012093 absent nodal flow IAGP N RGD:5509061 20141003 MGI PMID:10549278 1620923 Dnah11 dynein, axonemal, heavy chain 11 gene MP:0012093 absent nodal flow IAGP N RGD:5509061 20141003 MGI PMID:10556073 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:8682296 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9463357 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:8682296 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:8682296 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:8682296 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:9463357 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:8682296 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:9463357 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:10894154 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:10894154 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8682296 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:9463357 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20141003 MGI PMID:8682296 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:10894154 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10894154 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10894154 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0004558 delayed allantois development IAGP N RGD:5509061 20141003 MGI PMID:10894154 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0004559 small allantois IAGP N RGD:5509061 20141003 MGI PMID:10894154 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:8682296 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:8682296 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0004934 epididymis epithelium degeneration IAGP N RGD:5509061 20141003 MGI PMID:9463357 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8682296 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8682296 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9463357 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0008391 abnormal primordial germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10894154 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10894154 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0008393 absent primordial germ cells IAGP N RGD:5509061 20141003 MGI PMID:10894154 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10894154 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8682296 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9463357 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0013600 testis degeneration IAGP N RGD:5509061 20150312 MGI PMID:8682296 1620925 Bmp8b bone morphogenetic protein 8b gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:8682296 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:9463357 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11784057 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:9463357 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:9463357 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11784057 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:9463357 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:11784057 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:9463357 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:11784057 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:9463357 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11784057 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0004934 epididymis epithelium degeneration IAGP N RGD:5509061 20141003 MGI PMID:11784057 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0004934 epididymis epithelium degeneration IAGP N RGD:5509061 20141003 MGI PMID:9463357 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0004935 epididymis degeneration IAGP N RGD:5509061 20141003 MGI PMID:11784057 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11784057 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9463357 1620926 Bmp8a bone morphogenetic protein 8a gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:9463357 1620927 Hrk harakiri, BCL2 interacting protein (contains only BH3 domain) gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:17535852 1620927 Hrk harakiri, BCL2 interacting protein (contains only BH3 domain) gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:15084651 1620927 Hrk harakiri, BCL2 interacting protein (contains only BH3 domain) gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20200310 MGI PMID:15084651 1620927 Hrk harakiri, BCL2 interacting protein (contains only BH3 domain) gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:15084651 1620927 Hrk harakiri, BCL2 interacting protein (contains only BH3 domain) gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:17535852 1621047 Btnl4 butyrophilin-like 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200310 MGI 1621047 Btnl4 butyrophilin-like 4 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20200310 MGI 1621047 Btnl4 butyrophilin-like 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20200310 MGI 1621047 Btnl4 butyrophilin-like 4 gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20220519 MGI 1621047 Btnl4 butyrophilin-like 4 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 1621047 Btnl4 butyrophilin-like 4 gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20211021 MGI 1621096 Fscb fibrous sheath CABYR binding protein gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1621096 Fscb fibrous sheath CABYR binding protein gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230601 MGI 1621096 Fscb fibrous sheath CABYR binding protein gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20231207 MGI 1621096 Fscb fibrous sheath CABYR binding protein gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20231207 MGI 1621096 Fscb fibrous sheath CABYR binding protein gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201022 MGI PMID:32588039 1621096 Fscb fibrous sheath CABYR binding protein gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20231207 MGI 1621132 Wdfy4 WD repeat and FYVE domain containing 4 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1621132 Wdfy4 WD repeat and FYVE domain containing 4 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20230601 MGI 1621132 Wdfy4 WD repeat and FYVE domain containing 4 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20231109 MGI PMID:35617964 1621132 Wdfy4 WD repeat and FYVE domain containing 4 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20231109 MGI PMID:35617964 1621147 Tmprss11c transmembrane protease, serine 11c gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20191031 MGI PMID:31501243 1621149 Rnf223 ring finger 223 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1621149 Rnf223 ring finger 223 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1621149 Rnf223 ring finger 223 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1621149 Rnf223 ring finger 223 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1621149 Rnf223 ring finger 223 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1621149 Rnf223 ring finger 223 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1621149 Rnf223 ring finger 223 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1621149 Rnf223 ring finger 223 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1621149 Rnf223 ring finger 223 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1621149 Rnf223 ring finger 223 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1621149 Rnf223 ring finger 223 gene MP:0003604 single kidney IEA N RGD:5509061 20210128 MGI 1621153 Psg20 pregnancy-specific beta-1-glycoprotein 20 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1621153 Psg20 pregnancy-specific beta-1-glycoprotein 20 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1621157 Mettl21c methyltransferase 21C, AARS1 lysine gene MP:0000747 muscle weakness IAGP N RGD:5509061 20190314 MGI PMID:29719249 1621157 Mettl21c methyltransferase 21C, AARS1 lysine gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20190314 MGI PMID:29719249 1621157 Mettl21c methyltransferase 21C, AARS1 lysine gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20190314 MGI PMID:29719249 1621157 Mettl21c methyltransferase 21C, AARS1 lysine gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20190314 MGI PMID:29719249 1621172 Clec3a C-type lectin domain family 3, member a gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20211021 MGI 1621172 Clec3a C-type lectin domain family 3, member a gene MP:0001284 absent vibrissae IEA N RGD:5509061 20210128 MGI 1621172 Clec3a C-type lectin domain family 3, member a gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1621172 Clec3a C-type lectin domain family 3, member a gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1621172 Clec3a C-type lectin domain family 3, member a gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1621172 Clec3a C-type lectin domain family 3, member a gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20211021 MGI 1621173 Serpinb3d serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 3D gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 1621174 Cdsn corneodesmosin gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18436651 1621174 Cdsn corneodesmosin gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:18436651 1621174 Cdsn corneodesmosin gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0001193 psoriasis IAGP N RGD:5509061 20170309 MGI PMID:18436651 1621174 Cdsn corneodesmosin gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18436651 1621174 Cdsn corneodesmosin gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:18436651 1621174 Cdsn corneodesmosin gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:18436651 1621174 Cdsn corneodesmosin gene MP:0001241 absent epidermis stratum corneum IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:18436651 1621174 Cdsn corneodesmosin gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:18436651 1621174 Cdsn corneodesmosin gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:18436651 1621174 Cdsn corneodesmosin gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:18436651 1621174 Cdsn corneodesmosin gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:18436651 1621174 Cdsn corneodesmosin gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:18436651 1621174 Cdsn corneodesmosin gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:18436651 1621174 Cdsn corneodesmosin gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1621174 Cdsn corneodesmosin gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1621174 Cdsn corneodesmosin gene MP:0009793 sebaceous gland hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0010699 dilated hair follicle IAGP N RGD:5509061 20240620 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18436651 1621174 Cdsn corneodesmosin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19596793 1621174 Cdsn corneodesmosin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1621174 Cdsn corneodesmosin gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20181227 MGI 1621180 Kcnf1 potassium voltage-gated channel, subfamily F, member 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210128 MGI 1621180 Kcnf1 potassium voltage-gated channel, subfamily F, member 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1621180 Kcnf1 potassium voltage-gated channel, subfamily F, member 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1621180 Kcnf1 potassium voltage-gated channel, subfamily F, member 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1621180 Kcnf1 potassium voltage-gated channel, subfamily F, member 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1621183 Ankfn1 ankyrin-repeat and fibronectin type III domain containing 1 gene MP:0000745 tremors IAGP N RGD:5509061 20160114 MGI PMID:26131556 1621183 Ankfn1 ankyrin-repeat and fibronectin type III domain containing 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160114 MGI PMID:26131556 1621183 Ankfn1 ankyrin-repeat and fibronectin type III domain containing 1 gene MP:0001394 circling IAGP N RGD:5509061 20160114 MGI PMID:26131556 1621183 Ankfn1 ankyrin-repeat and fibronectin type III domain containing 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160114 MGI PMID:26131556 1621183 Ankfn1 ankyrin-repeat and fibronectin type III domain containing 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20160114 MGI PMID:26131556 1621183 Ankfn1 ankyrin-repeat and fibronectin type III domain containing 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20160114 MGI PMID:26131556 1621183 Ankfn1 ankyrin-repeat and fibronectin type III domain containing 1 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20160114 MGI PMID:26131556 1621183 Ankfn1 ankyrin-repeat and fibronectin type III domain containing 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20160114 MGI PMID:26131556 1621183 Ankfn1 ankyrin-repeat and fibronectin type III domain containing 1 gene MP:0005191 head tilt IAGP N RGD:5509061 20160114 MGI PMID:26131556 1621183 Ankfn1 ankyrin-repeat and fibronectin type III domain containing 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20160114 MGI PMID:26131556 1621183 Ankfn1 ankyrin-repeat and fibronectin type III domain containing 1 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20160114 MGI PMID:26131556 1621183 Ankfn1 ankyrin-repeat and fibronectin type III domain containing 1 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:26131556 1621183 Ankfn1 ankyrin-repeat and fibronectin type III domain containing 1 gene MP:0020468 abnormal circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:26131556 1621183 Ankfn1 ankyrin-repeat and fibronectin type III domain containing 1 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:26131556 1621185 Kif14 kinesin family member 14 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0010012 ectopic cerebral cortex pyramidal cells IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23308235 1621185 Kif14 kinesin family member 14 gene MP:0012174 flat head IAGP N RGD:5509061 20171123 MGI PMID:23308235 1621187 Crocc2 ciliary rootlet coiled-coil, rootletin family member 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240523 MGI 1621187 Crocc2 ciliary rootlet coiled-coil, rootletin family member 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20240523 MGI 1621187 Crocc2 ciliary rootlet coiled-coil, rootletin family member 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 1621187 Crocc2 ciliary rootlet coiled-coil, rootletin family member 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 1621187 Crocc2 ciliary rootlet coiled-coil, rootletin family member 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20240523 MGI 1621187 Crocc2 ciliary rootlet coiled-coil, rootletin family member 2 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20240523 MGI 1621189 Mreg melanoregulin gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:2379821 1621189 Mreg melanoregulin gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:3410303 1621189 Mreg melanoregulin gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1621189 Mreg melanoregulin gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:2379821 1621189 Mreg melanoregulin gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1621189 Mreg melanoregulin gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:6886377 1621189 Mreg melanoregulin gene MP:0002880 opisthotonus IAGP N RGD:5509061 20141003 MGI PMID:3141922 1621189 Mreg melanoregulin gene MP:0003171 phenotypic reversion IAGP N RGD:5509061 20141003 MGI PMID:2379821 1621189 Mreg melanoregulin gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1621189 Mreg melanoregulin gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20221215 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20220811 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200514 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200514 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20200514 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20200514 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20200514 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200514 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0001147 small testis IEA N RGD:5509061 20200514 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20220811 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20200514 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20200514 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20200514 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20220811 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0004357 long tibia IEA N RGD:5509061 20211021 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0005238 increased brain size IEA N RGD:5509061 20200514 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 1621191 Tmem237 transmembrane protein 237 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1621194 Cfap58 cilia and flagella associated protein 58 gene MP:0001925 male infertility IAGP N RGD:5509061 20201217 MGI PMID:32791035 1621194 Cfap58 cilia and flagella associated protein 58 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20201217 MGI PMID:32791035 1621194 Cfap58 cilia and flagella associated protein 58 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20201217 MGI PMID:32791035 1621194 Cfap58 cilia and flagella associated protein 58 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20201217 MGI PMID:32791035 1621194 Cfap58 cilia and flagella associated protein 58 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20201217 MGI PMID:32791035 1621194 Cfap58 cilia and flagella associated protein 58 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20201217 MGI PMID:32791035 1621194 Cfap58 cilia and flagella associated protein 58 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20201217 MGI PMID:32791035 1621195 Hpse2 heparanase 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 1621195 Hpse2 heparanase 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1621195 Hpse2 heparanase 2 gene MP:0001761 abnormal urination pattern IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0003280 urinary incontinence IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20201022 MGI 1621195 Hpse2 heparanase 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1621195 Hpse2 heparanase 2 gene MP:0011535 increased urination frequency IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621195 Hpse2 heparanase 2 gene MP:0011769 urinary bladder fibrosis IAGP N RGD:5509061 20151112 MGI PMID:25510506 1621202 Brcc3dc BRCA1/BRCA2-containing complex, subunit 3, domain containing gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230601 MGI 1621203 Prss48 serine protease 48 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1621203 Prss48 serine protease 48 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1621203 Prss48 serine protease 48 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1621203 Prss48 serine protease 48 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20230119 MGI 1621203 Prss48 serine protease 48 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230119 MGI 1621203 Prss48 serine protease 48 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1621203 Prss48 serine protease 48 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 1621203 Prss48 serine protease 48 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1621203 Prss48 serine protease 48 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20230119 MGI 1621203 Prss48 serine protease 48 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230119 MGI 1621203 Prss48 serine protease 48 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20230119 MGI 1621203 Prss48 serine protease 48 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20230119 MGI 1621204 Ifnl3 interferon lambda 3 gene MP:0002418 increased susceptibility to viral infection IAGP N RGD:5509061 20210527 MGI PMID:31462571 1621204 Ifnl3 interferon lambda 3 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220519 MGI 1621204 Ifnl3 interferon lambda 3 gene MP:0008548 abnormal circulating interferon level IAGP N RGD:5509061 20210527 MGI PMID:31462571 1621204 Ifnl3 interferon lambda 3 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20210527 MGI PMID:31462571 1621204 Ifnl3 interferon lambda 3 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20210527 MGI PMID:31462571 1621205 Nalcn sodium leak channel, non-selective gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1621205 Nalcn sodium leak channel, non-selective gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1621205 Nalcn sodium leak channel, non-selective gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1621205 Nalcn sodium leak channel, non-selective gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1621205 Nalcn sodium leak channel, non-selective gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1621205 Nalcn sodium leak channel, non-selective gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1621205 Nalcn sodium leak channel, non-selective gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1621205 Nalcn sodium leak channel, non-selective gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1621205 Nalcn sodium leak channel, non-selective gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1621205 Nalcn sodium leak channel, non-selective gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:17448995 1621205 Nalcn sodium leak channel, non-selective gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:17448995 1621205 Nalcn sodium leak channel, non-selective gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1621205 Nalcn sodium leak channel, non-selective gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17448995 1621205 Nalcn sodium leak channel, non-selective gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20161124 MGI PMID:27806374 1621205 Nalcn sodium leak channel, non-selective gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20170223 MGI PMID:26276633 1621205 Nalcn sodium leak channel, non-selective gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20170223 MGI PMID:26276633 1621205 Nalcn sodium leak channel, non-selective gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1621205 Nalcn sodium leak channel, non-selective gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:17448995 1621205 Nalcn sodium leak channel, non-selective gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20161124 MGI PMID:27806374 1621205 Nalcn sodium leak channel, non-selective gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:17448995 1621205 Nalcn sodium leak channel, non-selective gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17448995 1621205 Nalcn sodium leak channel, non-selective gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20240523 MGI 1621205 Nalcn sodium leak channel, non-selective gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20170223 MGI PMID:26276633 1621205 Nalcn sodium leak channel, non-selective gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17448995 1621205 Nalcn sodium leak channel, non-selective gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1621205 Nalcn sodium leak channel, non-selective gene MP:0012288 abnormal paradoxical sleep pattern IAGP N RGD:5509061 20161124 MGI PMID:27806374 1621205 Nalcn sodium leak channel, non-selective gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:27806374 1621206 Myo1d myosin ID gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1621206 Myo1d myosin ID gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20181227 MGI 1621206 Myo1d myosin ID gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1621206 Myo1d myosin ID gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20190103 MGI PMID:30279225 1621206 Myo1d myosin ID gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20190103 MGI PMID:30279225 1621206 Myo1d myosin ID gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20190103 MGI PMID:30279225 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0010870 absent bone trabeculae IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21606205 1621207 Mia3 MIA SH3 domain ER export factor 3 gene MP:0020138 delayed bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:21606205 1621208 Trim65 tripartite motif-containing 65 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20211202 MGI PMID:28031478 1621208 Trim65 tripartite motif-containing 65 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20211202 MGI PMID:28031478 1621208 Trim65 tripartite motif-containing 65 gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20211202 MGI PMID:28031478 1621208 Trim65 tripartite motif-containing 65 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20211202 MGI PMID:28031478 1621208 Trim65 tripartite motif-containing 65 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20211202 MGI PMID:28031478 1621208 Trim65 tripartite motif-containing 65 gene MP:0031040 increased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20211202 MGI PMID:28031478 1621212 Nell1 NEL-like 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1621212 Nell1 NEL-like 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1621212 Nell1 NEL-like 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1621212 Nell1 NEL-like 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1621212 Nell1 NEL-like 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20230601 MGI PMID:35700263 1621212 Nell1 NEL-like 1 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0004375 enlarged frontal bone IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0004386 enlarged interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0004421 enlarged parietal bone IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0004474 enlarged nasal bone IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1621212 Nell1 NEL-like 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1621212 Nell1 NEL-like 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11792855 1621212 Nell1 NEL-like 1 gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1621212 Nell1 NEL-like 1 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:35700263 1621212 Nell1 NEL-like 1 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0021056 abnormal tumor vascular morphology IAGP N RGD:5509061 20230601 MGI PMID:35700263 1621212 Nell1 NEL-like 1 gene MP:0030275 thin frontal bone IAGP N RGD:5509061 20171102 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0030277 thin interparietal bone IAGP N RGD:5509061 20171102 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0030281 thin parietal bone IAGP N RGD:5509061 20171102 MGI PMID:16537572 1621212 Nell1 NEL-like 1 gene MP:0031278 decreased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:35700263 1621213 Acad12 acyl-Coenzyme A dehydrogenase family, member 12 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1621214 Cntln centlein, centrosomal protein gene MP:0001925 male infertility IAGP N RGD:5509061 20220630 MGI PMID:34389728 1621214 Cntln centlein, centrosomal protein gene MP:0009234 absent sperm head IAGP N RGD:5509061 20220630 MGI PMID:34389728 1621215 Gpr21 G protein-coupled receptor 21 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22155242 1621215 Gpr21 G protein-coupled receptor 21 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:22155242 1621215 Gpr21 G protein-coupled receptor 21 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:22155242 1621215 Gpr21 G protein-coupled receptor 21 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22155242 1621215 Gpr21 G protein-coupled receptor 21 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:22155242 1621215 Gpr21 G protein-coupled receptor 21 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22155242 1621215 Gpr21 G protein-coupled receptor 21 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:22155242 1621215 Gpr21 G protein-coupled receptor 21 gene MP:0031233 decreased circulating serum amyloid protein level IAGP N RGD:5509061 20210225 MGI PMID:22155242 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20190321 MGI PMID:27026368 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20170601 MGI PMID:26980188 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20170608 MGI PMID:26980189 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20170601 MGI PMID:26980188 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20170608 MGI PMID:26980189 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20210121 MGI PMID:32876667 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20190321 MGI PMID:27026368 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0003325 decreased liver function IAGP N RGD:5509061 20170608 MGI PMID:26980189 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0004025 polyploidy IAGP N RGD:5509061 20170601 MGI PMID:26980188 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0004025 polyploidy IAGP N RGD:5509061 20170608 MGI PMID:26980189 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20170608 MGI PMID:26980189 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20190321 MGI PMID:27026368 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20190321 MGI PMID:27026368 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20210121 MGI PMID:32876667 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20170601 MGI PMID:26980188 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0008402 increased cellular sensitivity to alkylating agents IAGP N RGD:5509061 20210121 MGI PMID:32876667 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20170601 MGI PMID:26980188 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20170608 MGI PMID:26980189 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20190321 MGI PMID:27026368 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20190321 MGI PMID:27026368 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20170601 MGI PMID:26980188 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20170608 MGI PMID:26980189 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20190321 MGI PMID:27026368 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20170608 MGI PMID:26980189 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20170601 MGI PMID:26980188 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20190321 MGI PMID:27026368 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20190321 MGI PMID:27026368 1621218 Fan1 FANCD2/FANCI-associated nuclease 1 gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20170803 MGI PMID:26980189 1621223 Zfp82 zinc finger protein 82 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20220120 MGI PMID:34615997 1621223 Zfp82 zinc finger protein 82 gene MP:0012436 increased colon tumor incidence IAGP N RGD:5509061 20220120 MGI PMID:34615997 1621224 Fam163a family with sequence similarity 163, member A gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210520 MGI 1621224 Fam163a family with sequence similarity 163, member A gene MP:0001258 decreased body length IEA N RGD:5509061 20181227 MGI 1621224 Fam163a family with sequence similarity 163, member A gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20210520 MGI 1621224 Fam163a family with sequence similarity 163, member A gene MP:0002546 mydriasis IEA N RGD:5509061 20210520 MGI 1621224 Fam163a family with sequence similarity 163, member A gene MP:0002608 increased hematocrit IEA N RGD:5509061 20210520 MGI 1621224 Fam163a family with sequence similarity 163, member A gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1621224 Fam163a family with sequence similarity 163, member A gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20210520 MGI 1621224 Fam163a family with sequence similarity 163, member A gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1621224 Fam163a family with sequence similarity 163, member A gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210520 MGI 1621224 Fam163a family with sequence similarity 163, member A gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1621224 Fam163a family with sequence similarity 163, member A gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210520 MGI 1621224 Fam163a family with sequence similarity 163, member A gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20181227 MGI 1621224 Fam163a family with sequence similarity 163, member A gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1621225 Dennd1b DENN domain containing 1B gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20180222 MGI PMID:26774822 1621225 Dennd1b DENN domain containing 1B gene MP:0004882 enlarged lung IAGP N RGD:5509061 20180222 MGI PMID:26774822 1621225 Dennd1b DENN domain containing 1B gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20180222 MGI PMID:26774822 1621225 Dennd1b DENN domain containing 1B gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20180222 MGI PMID:26774822 1621225 Dennd1b DENN domain containing 1B gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20180222 MGI PMID:26774822 1621225 Dennd1b DENN domain containing 1B gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20180222 MGI PMID:26774822 1621227 Rbm44 RNA binding motif protein 44 gene MP:0001934 increased litter size IAGP N RGD:5509061 20141003 MGI PMID:21364893 1621227 Rbm44 RNA binding motif protein 44 gene MP:0030603 increased sperm number IAGP N RGD:5509061 20220714 MGI PMID:21364893 1621227 Rbm44 RNA binding motif protein 44 gene MP:0031425 enhanced male fertility IAGP N RGD:5509061 20220714 MGI PMID:21364893 1621228 Hsf5 heat shock transcription factor family member 5 gene MP:0001147 small testis IAGP N RGD:5509061 20240829 MGI PMID:37206036 1621228 Hsf5 heat shock transcription factor family member 5 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20240829 MGI PMID:37206036 1621228 Hsf5 heat shock transcription factor family member 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20240829 MGI PMID:37206036 1621228 Hsf5 heat shock transcription factor family member 5 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1621228 Hsf5 heat shock transcription factor family member 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20240829 MGI PMID:37206036 1621228 Hsf5 heat shock transcription factor family member 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20240829 MGI PMID:37206036 1621228 Hsf5 heat shock transcription factor family member 5 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20240829 MGI PMID:37206036 1621228 Hsf5 heat shock transcription factor family member 5 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20240523 MGI 1621228 Hsf5 heat shock transcription factor family member 5 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20240829 MGI PMID:37206036 1621228 Hsf5 heat shock transcription factor family member 5 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1621228 Hsf5 heat shock transcription factor family member 5 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1621228 Hsf5 heat shock transcription factor family member 5 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20240829 MGI PMID:37206036 1621230 Zfp616 zinc finger protein 616 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1621230 Zfp616 zinc finger protein 616 gene MP:0013775 increased KLRG1-positive T-helper cell number IEA N RGD:5509061 20201231 MGI 1621232 Pitpnm3 PITPNM family member 3 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1621232 Pitpnm3 PITPNM family member 3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1621233 Scimp SLP adaptor and CSK interacting membrane protein gene MP:0001260 increased body weight IEA N RGD:5509061 20141003 MGI 1621233 Scimp SLP adaptor and CSK interacting membrane protein gene MP:0001577 anemia IEA N RGD:5509061 20141003 MGI 1621233 Scimp SLP adaptor and CSK interacting membrane protein gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20141003 MGI 1621235 Cyb5d1 cytochrome b5 domain containing 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1621235 Cyb5d1 cytochrome b5 domain containing 1 gene MP:0000947 convulsive seizures IEA N RGD:5509061 20211021 MGI 1621235 Cyb5d1 cytochrome b5 domain containing 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1621235 Cyb5d1 cytochrome b5 domain containing 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1621235 Cyb5d1 cytochrome b5 domain containing 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20240523 MGI 1621235 Cyb5d1 cytochrome b5 domain containing 1 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20160421 MGI 1621235 Cyb5d1 cytochrome b5 domain containing 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20170105 MGI 1621235 Cyb5d1 cytochrome b5 domain containing 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20170105 MGI 1621235 Cyb5d1 cytochrome b5 domain containing 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1621235 Cyb5d1 cytochrome b5 domain containing 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 1621240 BC049715 cDNA sequence BC049715 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1621240 BC049715 cDNA sequence BC049715 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 1621240 BC049715 cDNA sequence BC049715 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1621241 Dgki diacylglycerol kinase, iota gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20201022 MGI PMID:32492392 1621241 Dgki diacylglycerol kinase, iota gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1621241 Dgki diacylglycerol kinase, iota gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20220714 MGI PMID:30985063 1621241 Dgki diacylglycerol kinase, iota gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20220714 MGI PMID:30985063 1621241 Dgki diacylglycerol kinase, iota gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20220714 MGI PMID:30985063 1621241 Dgki diacylglycerol kinase, iota gene MP:0001399 hyperactivity IAGP N RGD:5509061 20220714 MGI PMID:30985063 1621241 Dgki diacylglycerol kinase, iota gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20220714 MGI PMID:30985063 1621241 Dgki diacylglycerol kinase, iota gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:15894621 1621241 Dgki diacylglycerol kinase, iota gene MP:0003063 increased coping response IAGP N RGD:5509061 20220714 MGI PMID:30985063 1621241 Dgki diacylglycerol kinase, iota gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20201022 MGI PMID:32492392 1621241 Dgki diacylglycerol kinase, iota gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20201022 MGI PMID:32492392 1621241 Dgki diacylglycerol kinase, iota gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1621241 Dgki diacylglycerol kinase, iota gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20201022 MGI PMID:32492392 1621241 Dgki diacylglycerol kinase, iota gene MP:0020379 abnormal sucrose solution preference IAGP N RGD:5509061 20220714 MGI PMID:30985063 1621243 Fndc9 fibronectin type III domain containing 9 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210128 MGI 1621243 Fndc9 fibronectin type III domain containing 9 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1621243 Fndc9 fibronectin type III domain containing 9 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210520 MGI 1621243 Fndc9 fibronectin type III domain containing 9 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1621243 Fndc9 fibronectin type III domain containing 9 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1621243 Fndc9 fibronectin type III domain containing 9 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1621243 Fndc9 fibronectin type III domain containing 9 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1621243 Fndc9 fibronectin type III domain containing 9 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 1621243 Fndc9 fibronectin type III domain containing 9 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1621243 Fndc9 fibronectin type III domain containing 9 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20231207 MGI 1621243 Fndc9 fibronectin type III domain containing 9 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 1621243 Fndc9 fibronectin type III domain containing 9 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20181227 MGI 1621243 Fndc9 fibronectin type III domain containing 9 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1621243 Fndc9 fibronectin type III domain containing 9 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1621243 Fndc9 fibronectin type III domain containing 9 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0001258 decreased body length IEA N RGD:5509061 20201022 MGI 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0001265 decreased body size IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0001926 female infertility IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20230601 MGI 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200430 MGI PMID:25892958 1621246 Kdm3b KDM3B lysine (K)-specific demethylase 3B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20190502 MGI 1621251 Zfp512b zinc finger protein 512B gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1621252 Nav3 neuron navigator 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210128 MGI 1621252 Nav3 neuron navigator 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 1621252 Nav3 neuron navigator 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21078623 1621253 Nphp4 nephronophthisis 4 (juvenile) homolog (human) gene MP:0012671 retina spots IEA N RGD:5509061 20141003 MGI 1621264 Or1e21 olfactory receptor family 1 subfamily E member 21 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20230601 MGI 1621264 Or1e21 olfactory receptor family 1 subfamily E member 21 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 1621264 Or1e21 olfactory receptor family 1 subfamily E member 21 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1621264 Or1e21 olfactory receptor family 1 subfamily E member 21 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1621264 Or1e21 olfactory receptor family 1 subfamily E member 21 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20230601 MGI 1621264 Or1e21 olfactory receptor family 1 subfamily E member 21 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1621264 Or1e21 olfactory receptor family 1 subfamily E member 21 gene MP:0009709 hydrometra IEA N RGD:5509061 20230601 MGI 1621283 Glb1l2 galactosidase, beta 1-like 2 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20170406 MGI 1621283 Glb1l2 galactosidase, beta 1-like 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20170406 MGI 1621283 Glb1l2 galactosidase, beta 1-like 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20170406 MGI 1621283 Glb1l2 galactosidase, beta 1-like 2 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20170406 MGI 1621284 Dpy19l1 dpy-19 like C-mannosyltransferase 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200310 MGI 1621284 Dpy19l1 dpy-19 like C-mannosyltransferase 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200310 MGI 1621284 Dpy19l1 dpy-19 like C-mannosyltransferase 1 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20210128 MGI 1621284 Dpy19l1 dpy-19 like C-mannosyltransferase 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1621284 Dpy19l1 dpy-19 like C-mannosyltransferase 1 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1621284 Dpy19l1 dpy-19 like C-mannosyltransferase 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1621284 Dpy19l1 dpy-19 like C-mannosyltransferase 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1621284 Dpy19l1 dpy-19 like C-mannosyltransferase 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210128 MGI 1621284 Dpy19l1 dpy-19 like C-mannosyltransferase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1621285 Olfm2 olfactomedin 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20160225 MGI PMID:25218043 1621285 Olfm2 olfactomedin 2 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20160225 MGI PMID:25218043 1621285 Olfm2 olfactomedin 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160225 MGI PMID:25218043 1621285 Olfm2 olfactomedin 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160225 MGI PMID:25218043 1621285 Olfm2 olfactomedin 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20160225 MGI PMID:25218043 1621285 Olfm2 olfactomedin 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20160225 MGI PMID:25218043 1621285 Olfm2 olfactomedin 2 gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20160225 MGI PMID:25218043 1621287 Lrrtm4 leucine rich repeat transmembrane neuronal 4 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:23911104 1621287 Lrrtm4 leucine rich repeat transmembrane neuronal 4 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:23911104 1621287 Lrrtm4 leucine rich repeat transmembrane neuronal 4 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23911104 1621287 Lrrtm4 leucine rich repeat transmembrane neuronal 4 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:23911104 1621288 Igk immunoglobulin kappa chain complex gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:16543471 1621288 Igk immunoglobulin kappa chain complex gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:9430222 1621288 Igk immunoglobulin kappa chain complex gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20170713 MGI PMID:24591372 1621288 Igk immunoglobulin kappa chain complex gene MP:0001805 decreased IgG level IEA N RGD:5509061 20141003 MGI 1621288 Igk immunoglobulin kappa chain complex gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23940273 1621288 Igk immunoglobulin kappa chain complex gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20150129 MGI PMID:24706858 1621288 Igk immunoglobulin kappa chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11257137 1621288 Igk immunoglobulin kappa chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11869685 1621288 Igk immunoglobulin kappa chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12119344 1621288 Igk immunoglobulin kappa chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8658139 1621288 Igk immunoglobulin kappa chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8808678 1621288 Igk immunoglobulin kappa chain complex gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9430222 1621288 Igk immunoglobulin kappa chain complex gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19116268 1621288 Igk immunoglobulin kappa chain complex gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20170713 MGI PMID:24591372 1621288 Igk immunoglobulin kappa chain complex gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20170713 MGI PMID:24591372 1621288 Igk immunoglobulin kappa chain complex gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10639146 1621288 Igk immunoglobulin kappa chain complex gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18322191 1621288 Igk immunoglobulin kappa chain complex gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16973388 1621288 Igk immunoglobulin kappa chain complex gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:16543471 1621288 Igk immunoglobulin kappa chain complex gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:16543471 1621288 Igk immunoglobulin kappa chain complex gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20170713 MGI PMID:24591372 1621288 Igk immunoglobulin kappa chain complex gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12119344 1621288 Igk immunoglobulin kappa chain complex gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:17713479 1621288 Igk immunoglobulin kappa chain complex gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17713479 1621288 Igk immunoglobulin kappa chain complex gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16543471 1621288 Igk immunoglobulin kappa chain complex gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:17713479 1621288 Igk immunoglobulin kappa chain complex gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:19450527 1621288 Igk immunoglobulin kappa chain complex gene MP:0004942 abnormal B cell selection IAGP N RGD:5509061 20141003 MGI PMID:18322191 1621288 Igk immunoglobulin kappa chain complex gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11257137 1621288 Igk immunoglobulin kappa chain complex gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23940273 1621288 Igk immunoglobulin kappa chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11257137 1621288 Igk immunoglobulin kappa chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11869685 1621288 Igk immunoglobulin kappa chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12119344 1621288 Igk immunoglobulin kappa chain complex gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8808678 1621288 Igk immunoglobulin kappa chain complex gene MP:0005022 abnormal immature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14975236 1621288 Igk immunoglobulin kappa chain complex gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16973388 1621288 Igk immunoglobulin kappa chain complex gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20170713 MGI PMID:24591372 1621288 Igk immunoglobulin kappa chain complex gene MP:0008071 absent B cells IAGP N RGD:5509061 20170713 MGI PMID:24591372 1621288 Igk immunoglobulin kappa chain complex gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20170713 MGI PMID:24591372 1621288 Igk immunoglobulin kappa chain complex gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:16973388 1621288 Igk immunoglobulin kappa chain complex gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:16860389 1621288 Igk immunoglobulin kappa chain complex gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:11869685 1621288 Igk immunoglobulin kappa chain complex gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:12119344 1621288 Igk immunoglobulin kappa chain complex gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:17546032 1621288 Igk immunoglobulin kappa chain complex gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:8808678 1621288 Igk immunoglobulin kappa chain complex gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11869685 1621288 Igk immunoglobulin kappa chain complex gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18322191 1621288 Igk immunoglobulin kappa chain complex gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:8808678 1621288 Igk immunoglobulin kappa chain complex gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17546032 1621288 Igk immunoglobulin kappa chain complex gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11869685 1621288 Igk immunoglobulin kappa chain complex gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:23940273 1621288 Igk immunoglobulin kappa chain complex gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:8808678 1621288 Igk immunoglobulin kappa chain complex gene MP:0008822 decreased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:16543471 1621288 Igk immunoglobulin kappa chain complex gene MP:0009810 increased urine uric acid level IAGP N RGD:5509061 20141003 MGI PMID:16543471 1621288 Igk immunoglobulin kappa chain complex gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:11869685 1621288 Igk immunoglobulin kappa chain complex gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:11869685 1621288 Igk immunoglobulin kappa chain complex gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:16973388 1621288 Igk immunoglobulin kappa chain complex gene MP:0011352 proximal convoluted tubule brush border loss IAGP N RGD:5509061 20141003 MGI PMID:16543471 1621288 Igk immunoglobulin kappa chain complex gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:16973388 1621288 Igk immunoglobulin kappa chain complex gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:16973388 1621289 Kcna10 potassium voltage-gated channel, shaker-related subfamily, member 10 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200310 MGI 1621289 Kcna10 potassium voltage-gated channel, shaker-related subfamily, member 10 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200310 MGI 1621289 Kcna10 potassium voltage-gated channel, shaker-related subfamily, member 10 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1621289 Kcna10 potassium voltage-gated channel, shaker-related subfamily, member 10 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1621289 Kcna10 potassium voltage-gated channel, shaker-related subfamily, member 10 gene MP:0004812 abnormal linear vestibular evoked potential IAGP N RGD:5509061 20200310 MGI PMID:23528307 1621289 Kcna10 potassium voltage-gated channel, shaker-related subfamily, member 10 gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20200310 MGI PMID:23528307 1621289 Kcna10 potassium voltage-gated channel, shaker-related subfamily, member 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1621289 Kcna10 potassium voltage-gated channel, shaker-related subfamily, member 10 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:23528307 1621289 Kcna10 potassium voltage-gated channel, shaker-related subfamily, member 10 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1621290 Slc22a15 solute carrier family 22 (organic anion/cation transporter), member 15 gene MP:0002626 increased heart rate IEA N RGD:5509061 20210826 MGI 1621290 Slc22a15 solute carrier family 22 (organic anion/cation transporter), member 15 gene MP:0010507 shortened RR interval IEA N RGD:5509061 20220519 MGI 1621292 Styxl2 serine/threonine/tyrosine interacting like 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 1621295 Tor1aip2 torsin A interacting protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240328 MGI PMID:38194265 1621296 Teddm1a transmembrane epididymal protein 1A gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210826 MGI 1621296 Teddm1a transmembrane epididymal protein 1A gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1621296 Teddm1a transmembrane epididymal protein 1A gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20220519 MGI 1621296 Teddm1a transmembrane epididymal protein 1A gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1621296 Teddm1a transmembrane epididymal protein 1A gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1621298 A4galt alpha 1,4-galactosyltransferase gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16476743 1621298 A4galt alpha 1,4-galactosyltransferase gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16476743 1621298 A4galt alpha 1,4-galactosyltransferase gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16476743 1621299 Cacna1i calcium channel, voltage-dependent, alpha 1I subunit gene MP:0000601 small liver IEA N RGD:5509061 20160811 MGI 1621299 Cacna1i calcium channel, voltage-dependent, alpha 1I subunit gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20160811 MGI 1621299 Cacna1i calcium channel, voltage-dependent, alpha 1I subunit gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230720 MGI 1621299 Cacna1i calcium channel, voltage-dependent, alpha 1I subunit gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20160811 MGI 1621299 Cacna1i calcium channel, voltage-dependent, alpha 1I subunit gene MP:0002188 small heart IEA N RGD:5509061 20160811 MGI 1621299 Cacna1i calcium channel, voltage-dependent, alpha 1I subunit gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20210520 MGI PMID:32066662 1621299 Cacna1i calcium channel, voltage-dependent, alpha 1I subunit gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1621299 Cacna1i calcium channel, voltage-dependent, alpha 1I subunit gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20210128 MGI 1621299 Cacna1i calcium channel, voltage-dependent, alpha 1I subunit gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20210520 MGI PMID:32066662 1621299 Cacna1i calcium channel, voltage-dependent, alpha 1I subunit gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20210520 MGI PMID:32066662 1621299 Cacna1i calcium channel, voltage-dependent, alpha 1I subunit gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20210520 MGI PMID:32066662 1621299 Cacna1i calcium channel, voltage-dependent, alpha 1I subunit gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20210520 MGI PMID:32066662 1621300 Mief1 mitochondrial elongation factor 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1621300 Mief1 mitochondrial elongation factor 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1621300 Mief1 mitochondrial elongation factor 1 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210520 MGI 1621301 Foxred2 FAD-dependent oxidoreductase domain containing 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1621301 Foxred2 FAD-dependent oxidoreductase domain containing 2 gene MP:0001513 limb grasping IEA N RGD:5509061 20201231 MGI 1621303 Akap5 A kinase anchor protein 5 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18711127 1621303 Akap5 A kinase anchor protein 5 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18711127 1621303 Akap5 A kinase anchor protein 5 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:18711127 1621303 Akap5 A kinase anchor protein 5 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17972919 1621303 Akap5 A kinase anchor protein 5 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:18711127 1621303 Akap5 A kinase anchor protein 5 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20160128 MGI PMID:23100425 1621303 Akap5 A kinase anchor protein 5 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20160128 MGI PMID:23100425 1621303 Akap5 A kinase anchor protein 5 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22940692 1621303 Akap5 A kinase anchor protein 5 gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18711127 1621303 Akap5 A kinase anchor protein 5 gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20160128 MGI PMID:23100425 1621303 Akap5 A kinase anchor protein 5 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:18711127 1621303 Akap5 A kinase anchor protein 5 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:22940692 1621303 Akap5 A kinase anchor protein 5 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20160128 MGI PMID:23100425 1621303 Akap5 A kinase anchor protein 5 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20160128 MGI PMID:23100425 1621303 Akap5 A kinase anchor protein 5 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:22940692 1621303 Akap5 A kinase anchor protein 5 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:22940692 1621303 Akap5 A kinase anchor protein 5 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20160128 MGI PMID:23100425 1621303 Akap5 A kinase anchor protein 5 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20160128 MGI PMID:24835999 1621303 Akap5 A kinase anchor protein 5 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22940692 1621303 Akap5 A kinase anchor protein 5 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22940692 1621303 Akap5 A kinase anchor protein 5 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22940692 1621304 Kcnh5 potassium voltage-gated channel, subfamily H (eag-related), member 5 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20111116 MGI 1621304 Kcnh5 potassium voltage-gated channel, subfamily H (eag-related), member 5 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20111116 MGI 1621305 Rpl10l ribosomal protein L10-like gene MP:0001925 male infertility IAGP N RGD:5509061 20220224 MGI PMID:28502657 1621305 Rpl10l ribosomal protein L10-like gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20220224 MGI PMID:28502657 1621305 Rpl10l ribosomal protein L10-like gene MP:0005159 azoospermia IAGP N RGD:5509061 20220224 MGI PMID:28502657 1621305 Rpl10l ribosomal protein L10-like gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20220224 MGI PMID:28502657 1621305 Rpl10l ribosomal protein L10-like gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220224 MGI PMID:28502657 1621308 Acaa1b acetyl-Coenzyme A acyltransferase 1B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15589695 1621311 Setd2 SET domain containing 2 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1621311 Setd2 SET domain containing 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0002764 short tibia IEA N RGD:5509061 20170105 MGI 1621311 Setd2 SET domain containing 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20171109 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20180301 MGI PMID:28424246 1621311 Setd2 SET domain containing 2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1621311 Setd2 SET domain containing 2 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1621311 Setd2 SET domain containing 2 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20190502 MGI 1621311 Setd2 SET domain containing 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0012176 abnormal head development IAGP N RGD:5509061 20171109 MGI PMID:20133625 1621311 Setd2 SET domain containing 2 gene MP:0020516 abnormal visceral yolk sac mesenchyme morphology IAGP N RGD:5509061 20180125 MGI PMID:20133625 1621313 Camkv CaM kinase-like vesicle-associated gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210128 MGI 1621313 Camkv CaM kinase-like vesicle-associated gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1621313 Camkv CaM kinase-like vesicle-associated gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1621313 Camkv CaM kinase-like vesicle-associated gene MP:0009476 enlarged cecum IEA N RGD:5509061 20210128 MGI 1621313 Camkv CaM kinase-like vesicle-associated gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1621313 Camkv CaM kinase-like vesicle-associated gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1621317 Zfp930 zinc finger protein 930 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201022 MGI 1621317 Zfp930 zinc finger protein 930 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20201231 MGI 1621317 Zfp930 zinc finger protein 930 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 1621319 Ddx60 DExD/H box helicase 60 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170601 MGI PMID:26457795 1621319 Ddx60 DExD/H box helicase 60 gene MP:0008573 increased circulating interferon-alpha level IAGP N RGD:5509061 20170706 MGI PMID:25981042 1621319 Ddx60 DExD/H box helicase 60 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20170706 MGI PMID:25981042 1621319 Ddx60 DExD/H box helicase 60 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:25981042 1621319 Ddx60 DExD/H box helicase 60 gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:25981042 1621320 Cbr4 carbonyl reductase 4 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20230119 MGI 1621320 Cbr4 carbonyl reductase 4 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230119 MGI 1621320 Cbr4 carbonyl reductase 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1621323 Ffar3 free fatty acid receptor 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 1621323 Ffar3 free fatty acid receptor 3 gene MP:0000601 small liver IEA N RGD:5509061 20230119 MGI 1621323 Ffar3 free fatty acid receptor 3 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:21518883 1621323 Ffar3 free fatty acid receptor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18931303 1621323 Ffar3 free fatty acid receptor 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230119 MGI 1621323 Ffar3 free fatty acid receptor 3 gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:21518883 1621323 Ffar3 free fatty acid receptor 3 gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:18931303 1621323 Ffar3 free fatty acid receptor 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160602 MGI PMID:25581519 1621323 Ffar3 free fatty acid receptor 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 1621323 Ffar3 free fatty acid receptor 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1621323 Ffar3 free fatty acid receptor 3 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:21518883 1621323 Ffar3 free fatty acid receptor 3 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20160602 MGI PMID:25581519 1621323 Ffar3 free fatty acid receptor 3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230119 MGI 1621323 Ffar3 free fatty acid receptor 3 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20160602 MGI PMID:25581519 1621323 Ffar3 free fatty acid receptor 3 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:18931303 1621323 Ffar3 free fatty acid receptor 3 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:21518883 1621323 Ffar3 free fatty acid receptor 3 gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21518883 1621323 Ffar3 free fatty acid receptor 3 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21518883 1621323 Ffar3 free fatty acid receptor 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20160602 MGI PMID:25581519 1621323 Ffar3 free fatty acid receptor 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22190648 1621323 Ffar3 free fatty acid receptor 3 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:21518883 1621323 Ffar3 free fatty acid receptor 3 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18931303 1621323 Ffar3 free fatty acid receptor 3 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:21518883 1621323 Ffar3 free fatty acid receptor 3 gene MP:0005664 decreased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:21518883 1621323 Ffar3 free fatty acid receptor 3 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:20399779 1621323 Ffar3 free fatty acid receptor 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18931303 1621323 Ffar3 free fatty acid receptor 3 gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:18931303 1621323 Ffar3 free fatty acid receptor 3 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21518883 1621323 Ffar3 free fatty acid receptor 3 gene MP:0009253 abnormal sympathetic neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21518883 1621323 Ffar3 free fatty acid receptor 3 gene MP:0009284 abnormal sympathetic neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:21518883 1621323 Ffar3 free fatty acid receptor 3 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18931303 1621323 Ffar3 free fatty acid receptor 3 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:18931303 1621323 Ffar3 free fatty acid receptor 3 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:22190648 1621325 Alkbh6 alkB homolog 6 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1621325 Alkbh6 alkB homolog 6 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1621325 Alkbh6 alkB homolog 6 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1621327 Zfp420 zinc finger protein 420 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20240523 MGI 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20240523 MGI 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20240523 MGI 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0009233 enlarged sperm head IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0009235 small sperm head IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621330 Hipk4 homeodomain interacting protein kinase 4 gene MP:0030980 abnormal acroplaxome morphology IAGP N RGD:5509061 20220210 MGI PMID:32163033 1621336 Dennd1a DENN domain containing 1A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220811 MGI 1621336 Dennd1a DENN domain containing 1A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0000601 small liver IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0000603 pale liver IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20201022 MGI 1621336 Dennd1a DENN domain containing 1A gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20201022 MGI 1621336 Dennd1a DENN domain containing 1A gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20201022 MGI 1621336 Dennd1a DENN domain containing 1A gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20201022 MGI 1621336 Dennd1a DENN domain containing 1A gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20220811 MGI 1621336 Dennd1a DENN domain containing 1A gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0005238 increased brain size IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20201022 MGI 1621336 Dennd1a DENN domain containing 1A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1621336 Dennd1a DENN domain containing 1A gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0012091 increased midbrain size IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0012139 increased forebrain size IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0012236 abnormal cholangiocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0012265 increased hindbrain size IAGP N RGD:5509061 20200310 MGI PMID:30884041 1621336 Dennd1a DENN domain containing 1A gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1621336 Dennd1a DENN domain containing 1A gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1621339 Prrc2c proline-rich coiled-coil 2C gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20201022 MGI 1621339 Prrc2c proline-rich coiled-coil 2C gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1621339 Prrc2c proline-rich coiled-coil 2C gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1621339 Prrc2c proline-rich coiled-coil 2C gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 1621339 Prrc2c proline-rich coiled-coil 2C gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20201022 MGI 1621339 Prrc2c proline-rich coiled-coil 2C gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20201022 MGI 1621339 Prrc2c proline-rich coiled-coil 2C gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 1621339 Prrc2c proline-rich coiled-coil 2C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1621340 Suco SUN domain containing ossification factor gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1621340 Suco SUN domain containing ossification factor gene MP:0011642 abnormal bone collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0030279 thin neurocranium IAGP N RGD:5509061 20171102 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0030441 increased osteoblast apoptosis IAGP N RGD:5509061 20171221 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0030482 increased osteocyte number IAGP N RGD:5509061 20171221 MGI PMID:20440000 1621340 Suco SUN domain containing ossification factor gene MP:0030985 decreased circulating osteocalcin level IAGP N RGD:5509061 20201001 MGI PMID:20440000 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210128 MGI 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20210128 MGI 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20230601 MGI 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20210128 MGI 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20210128 MGI 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0004085 abnormal heartbeat IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20210128 MGI 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0009328 delayed heart looping IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23213483 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1621343 Fhod3 formin homology 2 domain containing 3 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1621344 Klhl14 kelch-like 14 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20200310 MGI PMID:29939266 1621344 Klhl14 kelch-like 14 gene MP:0008169 increased B-1b cell number IAGP N RGD:5509061 20200310 MGI PMID:29939266 1621344 Klhl14 kelch-like 14 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29939266 1621345 Dsg1b desmoglein 1 beta gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20150108 MGI 1621345 Dsg1b desmoglein 1 beta gene MP:0001304 cataract IEA N RGD:5509061 20150108 MGI 1621345 Dsg1b desmoglein 1 beta gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20141003 MGI 1621345 Dsg1b desmoglein 1 beta gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20150108 MGI 1621345 Dsg1b desmoglein 1 beta gene MP:0001340 abnormal eyelid morphology IEA N RGD:5509061 20141003 MGI 1621345 Dsg1b desmoglein 1 beta gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201022 MGI 1621345 Dsg1b desmoglein 1 beta gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 1621345 Dsg1b desmoglein 1 beta gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1621347 Marf1 meiosis regulator and mRNA stability 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:22442484 1621347 Marf1 meiosis regulator and mRNA stability 1 gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20141003 MGI PMID:22442484 1621350 Spryd3 SPRY domain containing 3 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1621350 Spryd3 SPRY domain containing 3 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1621350 Spryd3 SPRY domain containing 3 gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 1621350 Spryd3 SPRY domain containing 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1621350 Spryd3 SPRY domain containing 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160804 MGI 1621350 Spryd3 SPRY domain containing 3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 1621350 Spryd3 SPRY domain containing 3 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1621350 Spryd3 SPRY domain containing 3 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1621350 Spryd3 SPRY domain containing 3 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1621350 Spryd3 SPRY domain containing 3 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20181227 MGI 1621350 Spryd3 SPRY domain containing 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1621350 Spryd3 SPRY domain containing 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1621350 Spryd3 SPRY domain containing 3 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1621350 Spryd3 SPRY domain containing 3 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1621350 Spryd3 SPRY domain containing 3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1621355 Nol10 nucleolar protein 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20221215 MGI 1621355 Nol10 nucleolar protein 10 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221215 MGI 1621358 Abhd17a abhydrolase domain containing 17A gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20240530 MGI PMID:36097267 1621358 Abhd17a abhydrolase domain containing 17A gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20160114 MGI 1621359 Sbno2 strawberry notch 2 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20200310 MGI PMID:23980096 1621359 Sbno2 strawberry notch 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:23980096 1621359 Sbno2 strawberry notch 2 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20200310 MGI PMID:23980096 1621359 Sbno2 strawberry notch 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20200310 MGI PMID:23980096 1621359 Sbno2 strawberry notch 2 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:23980096 1621359 Sbno2 strawberry notch 2 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20200310 MGI PMID:23980096 1621359 Sbno2 strawberry notch 2 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20200310 MGI PMID:23980096 1621359 Sbno2 strawberry notch 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20200310 MGI PMID:23980096 1621359 Sbno2 strawberry notch 2 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20200310 MGI PMID:23980096 1621359 Sbno2 strawberry notch 2 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20200310 MGI PMID:23980096 1621359 Sbno2 strawberry notch 2 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20200310 MGI PMID:23980096 1621359 Sbno2 strawberry notch 2 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20200310 MGI PMID:23980096 1621359 Sbno2 strawberry notch 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23980096 1621359 Sbno2 strawberry notch 2 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20200310 MGI PMID:23980096 1621360 Wdr18 WD repeat domain 18 gene MP:0001513 limb grasping IEA N RGD:5509061 20220811 MGI 1621360 Wdr18 WD repeat domain 18 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0000111 cleft palate IEA N RGD:5509061 20170209 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0000276 heart right ventricle hypertrophy IEA N RGD:5509061 20170209 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0001293 anophthalmia IEA N RGD:5509061 20170209 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0001297 microphthalmia IEA N RGD:5509061 20170209 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0001625 cardiac hypertrophy IEA N RGD:5509061 20170209 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20170209 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0001890 anencephaly IEA N RGD:5509061 20170209 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20181227 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0002625 heart left ventricle hypertrophy IEA N RGD:5509061 20170209 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0002639 micrognathia IEA N RGD:5509061 20170209 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0005157 holoprosencephaly IEA N RGD:5509061 20170209 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20201022 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20170209 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20170209 MGI 1621362 Trappc10 trafficking protein particle complex 10 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170209 MGI 1621364 Map9 microtubule-associated protein 9 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20210211 MGI PMID:31662330 1621364 Map9 microtubule-associated protein 9 gene MP:0002083 premature death IAGP N RGD:5509061 20210211 MGI PMID:31662330 1621364 Map9 microtubule-associated protein 9 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20210211 MGI PMID:31662330 1621364 Map9 microtubule-associated protein 9 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20210211 MGI PMID:31662330 1621364 Map9 microtubule-associated protein 9 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20210211 MGI PMID:31662330 1621364 Map9 microtubule-associated protein 9 gene MP:0012436 increased colon tumor incidence IAGP N RGD:5509061 20210211 MGI PMID:31662330 1621364 Map9 microtubule-associated protein 9 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20210211 MGI PMID:31662330 1621364 Map9 microtubule-associated protein 9 gene MP:0030944 abnormal pericentriolar material morphology IAGP N RGD:5509061 20210211 MGI PMID:31662330 1621366 Bag2 BCL2-associated athanogene 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1621366 Bag2 BCL2-associated athanogene 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1621366 Bag2 BCL2-associated athanogene 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1621371 Fam91a1 family with sequence similarity 91, member A1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20240523 MGI 1621371 Fam91a1 family with sequence similarity 91, member A1 gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20240523 MGI 1621371 Fam91a1 family with sequence similarity 91, member A1 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20240523 MGI 1621371 Fam91a1 family with sequence similarity 91, member A1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1621371 Fam91a1 family with sequence similarity 91, member A1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20240523 MGI 1621371 Fam91a1 family with sequence similarity 91, member A1 gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 1621371 Fam91a1 family with sequence similarity 91, member A1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20160421 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160421 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20160421 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20160421 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0001258 decreased body length IEA N RGD:5509061 20160421 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0002764 short tibia IEA N RGD:5509061 20160421 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160421 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20160421 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20160421 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160421 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0005270 abnormal zygomatic bone morphology IEA N RGD:5509061 20160421 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0010052 increased grip strength IEA N RGD:5509061 20181227 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 1621374 Ttc28 tetratricopeptide repeat domain 28 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201022 MGI 1621375 Erich3 glutamate rich 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1621375 Erich3 glutamate rich 3 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210826 MGI 1621376 Trim40 tripartite motif-containing 40 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20191114 MGI PMID:29117565 1621376 Trim40 tripartite motif-containing 40 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20191114 MGI PMID:29117565 1621376 Trim40 tripartite motif-containing 40 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20191114 MGI PMID:29117565 1621376 Trim40 tripartite motif-containing 40 gene MP:0031023 decreased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:29117565 1621378 Gsc2 goosecoid homebox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9811926 1621378 Gsc2 goosecoid homebox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9811927 1621379 Rapgef6 Rap guanine nucleotide exchange factor (GEF) 6 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17538012 1621379 Rapgef6 Rap guanine nucleotide exchange factor (GEF) 6 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20150416 MGI PMID:24491570 1621379 Rapgef6 Rap guanine nucleotide exchange factor (GEF) 6 gene MP:0001147 small testis IAGP N RGD:5509061 20150416 MGI PMID:24491570 1621379 Rapgef6 Rap guanine nucleotide exchange factor (GEF) 6 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20150416 MGI PMID:24491570 1621379 Rapgef6 Rap guanine nucleotide exchange factor (GEF) 6 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20150416 MGI PMID:24491570 1621379 Rapgef6 Rap guanine nucleotide exchange factor (GEF) 6 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20150416 MGI PMID:24491570 1621379 Rapgef6 Rap guanine nucleotide exchange factor (GEF) 6 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20150416 MGI PMID:24491570 1621379 Rapgef6 Rap guanine nucleotide exchange factor (GEF) 6 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20150416 MGI PMID:24491570 1621379 Rapgef6 Rap guanine nucleotide exchange factor (GEF) 6 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20150416 MGI PMID:24491570 1621379 Rapgef6 Rap guanine nucleotide exchange factor (GEF) 6 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:17538012 1621379 Rapgef6 Rap guanine nucleotide exchange factor (GEF) 6 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20150416 MGI PMID:24491570 1621381 Peg10 paternally expressed 10 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:16341224 1621381 Peg10 paternally expressed 10 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:16341224 1621381 Peg10 paternally expressed 10 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16341224 1621381 Peg10 paternally expressed 10 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:16341224 1621381 Peg10 paternally expressed 10 gene MP:0008959 abnormal spongiotrophoblast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16341224 1621381 Peg10 paternally expressed 10 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16341224 1621389 Bmp2k BMP2 inducible kinase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20170504 MGI 1621389 Bmp2k BMP2 inducible kinase gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20211021 MGI 1621390 Col26a1 collagen, type XXVI, alpha 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1621390 Col26a1 collagen, type XXVI, alpha 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1621390 Col26a1 collagen, type XXVI, alpha 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1621391 Emid1 EMI domain containing 1 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20160804 MGI 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:10827969 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20211104 MGI PMID:34156984 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20211104 MGI PMID:34156984 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:10827969 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0001588 abnormal hemoglobin IAGP N RGD:5509061 20200310 MGI PMID:10827969 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0001954 respiratory distress IAGP N RGD:5509061 20200310 MGI PMID:10827969 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20211104 MGI PMID:34156984 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:10827969 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20211104 MGI PMID:34156984 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0005039 hypoxia IAGP N RGD:5509061 20200310 MGI PMID:10827969 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20200310 MGI PMID:10827969 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20211104 MGI PMID:34156984 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20200310 MGI PMID:10827969 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:10827969 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20211104 MGI PMID:34156984 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:34156984 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20211104 MGI PMID:34156984 1621393 Scn2a sodium channel, voltage-gated, type II, alpha gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:34156984 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15652482 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:18987029 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:18987029 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:18987029 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18987029 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15652482 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15652482 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15652482 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15652482 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15652482 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18987029 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15652482 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18987029 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:18987029 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:18987029 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0010235 abnormal retina inner limiting membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:18987029 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15652482 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231221 MGI PMID:15652482 1621394 Srsf1 serine and arginine-rich splicing factor 1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:18987029 1621395 Lmo1 LIM domain only 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210128 MGI 1621395 Lmo1 LIM domain only 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1621395 Lmo1 LIM domain only 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1621395 Lmo1 LIM domain only 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:14966285 1621395 Lmo1 LIM domain only 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14966285 1621395 Lmo1 LIM domain only 1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20201022 MGI 1621395 Lmo1 LIM domain only 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1621395 Lmo1 LIM domain only 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1621395 Lmo1 LIM domain only 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1621396 Lmo3 LIM domain only 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:14966285 1621396 Lmo3 LIM domain only 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14966285 1621397 Sri sorcin gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180628 MGI PMID:26822088 1621397 Sri sorcin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180628 MGI PMID:26822088 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20200310 MGI PMID:20978237 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20221215 MGI 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200310 MGI PMID:20978237 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20200310 MGI PMID:20978237 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20200310 MGI PMID:20978237 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:20978237 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20240523 MGI 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20200310 MGI PMID:20978237 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:20978237 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20200310 MGI PMID:20978237 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0003717 pallor IAGP N RGD:5509061 20200310 MGI PMID:20978237 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20200310 MGI PMID:20978237 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:20978237 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20200310 MGI 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20200310 MGI PMID:20978237 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:20978237 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20200310 MGI PMID:20978237 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20200310 MGI PMID:20978237 1621402 Arap3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20221215 MGI 1621404 Dph3 diphthamine biosynthesis 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16648478 1621404 Dph3 diphthamine biosynthesis 3 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:16648478 1621404 Dph3 diphthamine biosynthesis 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16648478 1621404 Dph3 diphthamine biosynthesis 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16648478 1621404 Dph3 diphthamine biosynthesis 3 gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:16648478 1621404 Dph3 diphthamine biosynthesis 3 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:16648478 1621404 Dph3 diphthamine biosynthesis 3 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16648478 1621404 Dph3 diphthamine biosynthesis 3 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:16648478 1621404 Dph3 diphthamine biosynthesis 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16648478 1621404 Dph3 diphthamine biosynthesis 3 gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16648478 1621404 Dph3 diphthamine biosynthesis 3 gene MP:0012509 neural tube degeneration IAGP N RGD:5509061 20141003 MGI PMID:16648478 1621406 Barhl2 BarH like homeobox 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:19339595 1621406 Barhl2 BarH like homeobox 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19339595 1621406 Barhl2 BarH like homeobox 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19339595 1621406 Barhl2 BarH like homeobox 2 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19339595 1621406 Barhl2 BarH like homeobox 2 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19339595 1621406 Barhl2 BarH like homeobox 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19339595 1621406 Barhl2 BarH like homeobox 2 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:19339595 1621406 Barhl2 BarH like homeobox 2 gene MP:0008105 increased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:19339595 1621406 Barhl2 BarH like homeobox 2 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:19339595 1621406 Barhl2 BarH like homeobox 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19339595 1621406 Barhl2 BarH like homeobox 2 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:19339595 1621406 Barhl2 BarH like homeobox 2 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:19339595 1621406 Barhl2 BarH like homeobox 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19339595 1621412 Meig1 meiosis expressed gene 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19805151 1621412 Meig1 meiosis expressed gene 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:20004656 1621412 Meig1 meiosis expressed gene 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19805151 1621412 Meig1 meiosis expressed gene 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20004656 1621412 Meig1 meiosis expressed gene 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220127 MGI PMID:23258628 1621412 Meig1 meiosis expressed gene 1 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20220127 MGI PMID:23258628 1621412 Meig1 meiosis expressed gene 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19805151 1621412 Meig1 meiosis expressed gene 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220127 MGI PMID:23258628 1621412 Meig1 meiosis expressed gene 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20004656 1621412 Meig1 meiosis expressed gene 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220127 MGI PMID:23258628 1621412 Meig1 meiosis expressed gene 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:19805151 1621412 Meig1 meiosis expressed gene 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20004656 1621412 Meig1 meiosis expressed gene 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220127 MGI PMID:23258628 1621412 Meig1 meiosis expressed gene 1 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20220127 MGI PMID:23258628 1621412 Meig1 meiosis expressed gene 1 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:19805151 1621412 Meig1 meiosis expressed gene 1 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20220127 MGI PMID:23258628 1621412 Meig1 meiosis expressed gene 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:20004656 1621412 Meig1 meiosis expressed gene 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:19805151 1621412 Meig1 meiosis expressed gene 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:20004656 1621412 Meig1 meiosis expressed gene 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220127 MGI PMID:23258628 1621412 Meig1 meiosis expressed gene 1 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220127 MGI PMID:23258628 1621412 Meig1 meiosis expressed gene 1 gene MP:0009233 enlarged sperm head IAGP N RGD:5509061 20141003 MGI PMID:20004656 1621412 Meig1 meiosis expressed gene 1 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20141003 MGI PMID:19805151 1621412 Meig1 meiosis expressed gene 1 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220127 MGI PMID:23258628 1621412 Meig1 meiosis expressed gene 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:20004656 1621412 Meig1 meiosis expressed gene 1 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20200227 MGI PMID:20004656 1621412 Meig1 meiosis expressed gene 1 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220127 MGI PMID:23258628 1621412 Meig1 meiosis expressed gene 1 gene MP:0031374 abnormal manchette assembly IAGP N RGD:5509061 20220407 MGI PMID:23258628 1621413 Zfp119a zinc finger protein 119a gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1621413 Zfp119a zinc finger protein 119a gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 1621415 Septin10 septin 10 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1621415 Septin10 septin 10 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1621415 Septin10 septin 10 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1621416 Firre functional intergenic repeating RNA element gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201029 MGI PMID:31738164 1621418 Trim68 tripartite motif-containing 68 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 1621419 Zfand2a zinc finger, AN1-type domain 2A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:16973439 1621422 Nlrp4f NLR family, pyrin domain containing 4F gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20200409 MGI PMID:31575650 1621422 Nlrp4f NLR family, pyrin domain containing 4F gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200409 MGI PMID:31575650 1621422 Nlrp4f NLR family, pyrin domain containing 4F gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200409 MGI PMID:31575650 1621422 Nlrp4f NLR family, pyrin domain containing 4F gene MP:0003718 maternal effect IAGP N RGD:5509061 20200409 MGI PMID:31575650 1621423 B3galnt2 UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1621423 B3galnt2 UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 1621423 B3galnt2 UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1621423 B3galnt2 UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1621424 Fam8a1 family with sequence similarity 8, member A1 gene MP:0001513 limb grasping IEA N RGD:5509061 20231207 MGI 1621424 Fam8a1 family with sequence similarity 8, member A1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230601 MGI 1621435 Tktl1 transketolase-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1621435 Tktl1 transketolase-like 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:21233279 1621435 Tktl1 transketolase-like 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:21233279 1621437 Cemip cell migration inducing protein, hyaluronan binding gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20180308 MGI PMID:28699206 1621437 Cemip cell migration inducing protein, hyaluronan binding gene MP:0002764 short tibia IAGP N RGD:5509061 20220721 MGI PMID:28284715 1621437 Cemip cell migration inducing protein, hyaluronan binding gene MP:0003109 short femur IAGP N RGD:5509061 20220721 MGI PMID:28284715 1621437 Cemip cell migration inducing protein, hyaluronan binding gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20220721 MGI PMID:28284715 1621437 Cemip cell migration inducing protein, hyaluronan binding gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20180308 MGI PMID:28699206 1621437 Cemip cell migration inducing protein, hyaluronan binding gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20220721 MGI PMID:28284715 1621437 Cemip cell migration inducing protein, hyaluronan binding gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20220721 MGI PMID:28284715 1621437 Cemip cell migration inducing protein, hyaluronan binding gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20220721 MGI PMID:28284715 1621437 Cemip cell migration inducing protein, hyaluronan binding gene MP:0011904 abnormal Schwann cell physiology IAGP N RGD:5509061 20180308 MGI PMID:28699206 1621438 Arl4d ADP-ribosylation factor-like 4D gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 1621438 Arl4d ADP-ribosylation factor-like 4D gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20141003 MGI 1621438 Arl4d ADP-ribosylation factor-like 4D gene MP:0001258 decreased body length IEA N RGD:5509061 20160804 MGI 1621438 Arl4d ADP-ribosylation factor-like 4D gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1621438 Arl4d ADP-ribosylation factor-like 4D gene MP:0003345 decreased rib number IEA N RGD:5509061 20160804 MGI 1621438 Arl4d ADP-ribosylation factor-like 4D gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20141003 MGI 1621438 Arl4d ADP-ribosylation factor-like 4D gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20160804 MGI 1621438 Arl4d ADP-ribosylation factor-like 4D gene MP:0004648 decreased thoracic vertebrae number IEA N RGD:5509061 20160804 MGI 1621438 Arl4d ADP-ribosylation factor-like 4D gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20160804 MGI 1621438 Arl4d ADP-ribosylation factor-like 4D gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20141003 MGI 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20200310 MGI PMID:15207913 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:12239568 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0001967 deafness IAGP N RGD:5509061 20200310 MGI PMID:15207913 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0001967 deafness IAGP N RGD:5509061 20200310 MGI PMID:27534441 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20200310 MGI PMID:15207913 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:15207913 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:12239568 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:15207913 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20200310 MGI PMID:12239568 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20200310 MGI PMID:18466744 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20200310 MGI PMID:18466744 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:12239568 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:15207913 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004413 absent cochlear microphonics IAGP N RGD:5509061 20200310 MGI PMID:12239568 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004414 decreased cochlear microphonics IAGP N RGD:5509061 20200310 MGI PMID:15319415 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004414 decreased cochlear microphonics IAGP N RGD:5509061 20200310 MGI PMID:15478431 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20200310 MGI PMID:15319415 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20200310 MGI PMID:15478431 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004430 abnormal Claudius cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15207913 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20200310 MGI PMID:18466744 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004435 abnormal cochlear outer hair cell electromotility IAGP N RGD:5509061 20200310 MGI PMID:17640919 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004436 absent cochlear outer hair cell electromotility IAGP N RGD:5509061 20200310 MGI PMID:12239568 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004437 decreased cochlear outer hair cell electromotility IAGP N RGD:5509061 20200310 MGI PMID:12239568 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004437 decreased cochlear outer hair cell electromotility IAGP N RGD:5509061 20200310 MGI PMID:18466744 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20200310 MGI PMID:15207913 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004466 short cochlear outer hair cells IAGP N RGD:5509061 20200310 MGI PMID:12239568 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004466 short cochlear outer hair cells IAGP N RGD:5509061 20200310 MGI PMID:15207913 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20200310 MGI PMID:12239568 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20200310 MGI PMID:15478431 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20200310 MGI PMID:16166160 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20200310 MGI PMID:15478431 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0004767 increased cochlear nerve compound action potential IAGP N RGD:5509061 20200310 MGI PMID:18466744 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20200310 MGI PMID:12239568 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20200310 MGI PMID:16166160 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0006336 abnormal otoacoustic response IAGP N RGD:5509061 20200310 MGI PMID:20142329 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:12239568 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:15207913 1621439 Slc26a5 solute carrier family 26, member 5 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200310 MGI PMID:21954035 1621440 Gpr84 G protein-coupled receptor 84 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1621440 Gpr84 G protein-coupled receptor 84 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:15993493 1621440 Gpr84 G protein-coupled receptor 84 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:15993493 1621440 Gpr84 G protein-coupled receptor 84 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15993493 1621440 Gpr84 G protein-coupled receptor 84 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:15993493 1621441 Cxcr6 C-X-C motif chemokine receptor 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10975845 1621441 Cxcr6 C-X-C motif chemokine receptor 6 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17413002 1621443 Sapcd1 suppressor APC domain containing 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20221215 MGI 1621444 Ndufv3 NADH:ubiquinone oxidoreductase core subunit V3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1621444 Ndufv3 NADH:ubiquinone oxidoreductase core subunit V3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 1621444 Ndufv3 NADH:ubiquinone oxidoreductase core subunit V3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1621446 Cul9 cullin 9 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20210128 MGI 1621446 Cul9 cullin 9 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1621446 Cul9 cullin 9 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1621446 Cul9 cullin 9 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1621446 Cul9 cullin 9 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1621446 Cul9 cullin 9 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21487039 1621446 Cul9 cullin 9 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21487039 1621446 Cul9 cullin 9 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21487039 1621446 Cul9 cullin 9 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21487039 1621446 Cul9 cullin 9 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21487039 1621446 Cul9 cullin 9 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1621446 Cul9 cullin 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15964813 1621446 Cul9 cullin 9 gene MP:0003036 vertebral transformation IEA N RGD:5509061 20210128 MGI 1621446 Cul9 cullin 9 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:21487039 1621446 Cul9 cullin 9 gene MP:0003364 increased insulinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21487039 1621446 Cul9 cullin 9 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:21487039 1621446 Cul9 cullin 9 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20210128 MGI 1621446 Cul9 cullin 9 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1621446 Cul9 cullin 9 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 1621446 Cul9 cullin 9 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21487039 1621446 Cul9 cullin 9 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21487039 1621446 Cul9 cullin 9 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21487039 1621446 Cul9 cullin 9 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:21487039 1621446 Cul9 cullin 9 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 1621446 Cul9 cullin 9 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21487039 1621446 Cul9 cullin 9 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20141003 MGI PMID:21487039 1621446 Cul9 cullin 9 gene MP:0011971 increased circulating lactate dehydrogenase level IEA N RGD:5509061 20211021 MGI 1621446 Cul9 cullin 9 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21487039 1621446 Cul9 cullin 9 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:21487039 1621448 Tanc2 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201022 MGI 1621448 Tanc2 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1621448 Tanc2 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1621448 Tanc2 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20221215 MGI 1621448 Tanc2 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 1621448 Tanc2 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20221215 MGI 1621448 Tanc2 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1621448 Tanc2 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220519 MGI 1621448 Tanc2 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1621448 Tanc2 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1621448 Tanc2 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 1621448 Tanc2 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20210128 MGI 1621448 Tanc2 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21068316 1621448 Tanc2 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220519 MGI 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0001147 small testis IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0001925 male infertility IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0009241 thick sperm flagellum IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20230601 MGI 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0030591 absent sperm fibrous sheath IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621450 Ccdc183 coiled-coil domain containing 183 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20240523 MGI PMID:37882665 1621451 Krt76 keratin 76 gene MP:0000416 sparse hair IAGP N RGD:5509061 20190124 MGI PMID:25340873 1621451 Krt76 keratin 76 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20150709 MGI PMID:24721909 1621451 Krt76 keratin 76 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20150709 MGI PMID:24721909 1621451 Krt76 keratin 76 gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 1621451 Krt76 keratin 76 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20150709 MGI PMID:24721909 1621451 Krt76 keratin 76 gene MP:0001195 flaky skin IAGP N RGD:5509061 20150709 MGI PMID:24721909 1621451 Krt76 keratin 76 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 1621451 Krt76 keratin 76 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20150709 MGI PMID:24721909 1621451 Krt76 keratin 76 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 1621451 Krt76 keratin 76 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20190124 MGI PMID:25340873 1621451 Krt76 keratin 76 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20150709 MGI PMID:24721909 1621451 Krt76 keratin 76 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20190124 MGI PMID:25340873 1621451 Krt76 keratin 76 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 1621451 Krt76 keratin 76 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20190124 MGI PMID:25340873 1621451 Krt76 keratin 76 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20190124 MGI PMID:25340873 1621451 Krt76 keratin 76 gene MP:0010179 rough coat IAGP N RGD:5509061 20190124 MGI PMID:25340873 1621451 Krt76 keratin 76 gene MP:0010206 pigment incontinence IAGP N RGD:5509061 20190124 MGI PMID:25340873 1621451 Krt76 keratin 76 gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20150709 MGI PMID:24721909 1621453 Cep83 centrosomal protein 83 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210422 MGI 1621453 Cep83 centrosomal protein 83 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210422 MGI 1621453 Cep83 centrosomal protein 83 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20221103 MGI 1621453 Cep83 centrosomal protein 83 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20210422 MGI 1621453 Cep83 centrosomal protein 83 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221103 MGI 1621453 Cep83 centrosomal protein 83 gene MP:0001785 edema IEA N RGD:5509061 20221103 MGI 1621453 Cep83 centrosomal protein 83 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20221103 MGI 1621453 Cep83 centrosomal protein 83 gene MP:0009709 hydrometra IEA N RGD:5509061 20210422 MGI 1621453 Cep83 centrosomal protein 83 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210422 MGI 1621453 Cep83 centrosomal protein 83 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 1621455 Mrap melanocortin 2 receptor accessory protein gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210520 MGI 1621455 Mrap melanocortin 2 receptor accessory protein gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210826 MGI 1621455 Mrap melanocortin 2 receptor accessory protein gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1621455 Mrap melanocortin 2 receptor accessory protein gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20200310 MGI PMID:29879378 1621455 Mrap melanocortin 2 receptor accessory protein gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20200310 MGI PMID:29879378 1621455 Mrap melanocortin 2 receptor accessory protein gene MP:0005129 increased adrenocorticotropin level IAGP N RGD:5509061 20200310 MGI PMID:29879378 1621455 Mrap melanocortin 2 receptor accessory protein gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20200310 MGI PMID:29879378 1621455 Mrap melanocortin 2 receptor accessory protein gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20200310 MGI PMID:29879378 1621455 Mrap melanocortin 2 receptor accessory protein gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20200310 MGI PMID:29879378 1621455 Mrap melanocortin 2 receptor accessory protein gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20200310 MGI PMID:29879378 1621455 Mrap melanocortin 2 receptor accessory protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29879378 1621455 Mrap melanocortin 2 receptor accessory protein gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29879378 1621455 Mrap melanocortin 2 receptor accessory protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1621455 Mrap melanocortin 2 receptor accessory protein gene MP:0013310 abnormal adrenal gland development IAGP N RGD:5509061 20200310 MGI PMID:29879378 1621455 Mrap melanocortin 2 receptor accessory protein gene MP:0013565 abnormal adrenal gland capsule morphology IAGP N RGD:5509061 20200310 MGI PMID:29879378 1621457 Col25a1 collagen, type XXV, alpha 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20160804 MGI PMID:24453327 1621457 Col25a1 collagen, type XXV, alpha 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20160804 MGI PMID:24453327 1621457 Col25a1 collagen, type XXV, alpha 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20160804 MGI PMID:24453327 1621457 Col25a1 collagen, type XXV, alpha 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20160804 MGI PMID:24453327 1621457 Col25a1 collagen, type XXV, alpha 1 gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20160804 MGI PMID:24453327 1621457 Col25a1 collagen, type XXV, alpha 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20160804 MGI PMID:24453327 1621457 Col25a1 collagen, type XXV, alpha 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20160804 MGI PMID:24453327 1621457 Col25a1 collagen, type XXV, alpha 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20160804 MGI PMID:24453327 1621457 Col25a1 collagen, type XXV, alpha 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20160804 MGI PMID:24453327 1621457 Col25a1 collagen, type XXV, alpha 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20160804 MGI PMID:24453327 1621457 Col25a1 collagen, type XXV, alpha 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20160804 MGI PMID:24453327 1621457 Col25a1 collagen, type XXV, alpha 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160804 MGI PMID:24453327 1621457 Col25a1 collagen, type XXV, alpha 1 gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20160804 MGI PMID:24453327 1621459 Ticrr TOPBP1-interacting checkpoint and replication regulator gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241010 MGI 1621459 Ticrr TOPBP1-interacting checkpoint and replication regulator gene MP:0003815 hairless IEA N RGD:5509061 20141003 MGI 1621459 Ticrr TOPBP1-interacting checkpoint and replication regulator gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241017 MGI 1621459 Ticrr TOPBP1-interacting checkpoint and replication regulator gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1621459 Ticrr TOPBP1-interacting checkpoint and replication regulator gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20241010 MGI 1621460 4930444P10Rik RIKEN cDNA 4930444P10 gene gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1621461 Cfap299 cilia and flagella associated protein 299 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15705853 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15705853 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:23790753 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15705853 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15705853 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:15705853 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:23790753 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23790753 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:15705853 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20220421 MGI PMID:23790753 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:15705853 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0008440 abnormal subplate morphology IAGP N RGD:5509061 20141003 MGI PMID:15705853 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0008442 disorganized cortical plate IAGP N RGD:5509061 20141003 MGI PMID:15705853 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:23790753 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15705853 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23790753 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:15705853 1621464 Brsk2 BR serine/threonine kinase 2 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:15705853 1621465 Rab11fip1 RAB11 family interacting protein 1 (class I) gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20180215 MGI PMID:28294115 1621465 Rab11fip1 RAB11 family interacting protein 1 (class I) gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20180913 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0001925 male infertility IAGP N RGD:5509061 20180913 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20180913 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20180913 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20180913 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20180913 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20180913 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20180913 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20180913 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20180913 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20180913 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20180913 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20180913 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20180913 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20180913 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220428 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0031373 abnormal manchette perinuclear ring morphology IAGP N RGD:5509061 20220407 MGI PMID:29907856 1621466 Dcaf17 DDB1 and CUL4 associated factor 17 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20220428 MGI PMID:29907856 1621471 Rbm12 RNA binding motif protein 12 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:22384391 1621471 Rbm12 RNA binding motif protein 12 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:22384391 1621471 Rbm12 RNA binding motif protein 12 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22384391 1621473 Mamstr MEF2 activating motif and SAP domain containing transcriptional regulator gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:22279050 1621473 Mamstr MEF2 activating motif and SAP domain containing transcriptional regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22279050 1621473 Mamstr MEF2 activating motif and SAP domain containing transcriptional regulator gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:22279050 1621473 Mamstr MEF2 activating motif and SAP domain containing transcriptional regulator gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:22279050 1621473 Mamstr MEF2 activating motif and SAP domain containing transcriptional regulator gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:22279050 1621473 Mamstr MEF2 activating motif and SAP domain containing transcriptional regulator gene MP:0009410 abnormal skeletal muscle satellite cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22279050 1621473 Mamstr MEF2 activating motif and SAP domain containing transcriptional regulator gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22279050 1621473 Mamstr MEF2 activating motif and SAP domain containing transcriptional regulator gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:22279050 1621473 Mamstr MEF2 activating motif and SAP domain containing transcriptional regulator gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22279050 1621473 Mamstr MEF2 activating motif and SAP domain containing transcriptional regulator gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:22279050 1621475 Stpg3 sperm tail PG rich repeat containing 3 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210708 MGI PMID:32561905 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20170105 MGI 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20170105 MGI 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210520 MGI 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20141003 MGI 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20220519 MGI 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20201022 MGI 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0005358 abnormal incisor morphology IEA N RGD:5509061 20201231 MGI 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0010912 herniated liver IEA N RGD:5509061 20170504 MGI 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1621478 Exoc3l2 exocyst complex component 3-like 2 gene MP:0013878 abnormal ductus venosus valve topology IEA N RGD:5509061 20170504 MGI 1621479 4933425B07Rik RIKEN cDNA 4933425B07 gene gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20230126 MGI PMID:33681192 1621479 4933425B07Rik RIKEN cDNA 4933425B07 gene gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20230126 MGI PMID:33681192 1621479 4933425B07Rik RIKEN cDNA 4933425B07 gene gene MP:0000524 decreased renal tubule number IAGP N RGD:5509061 20230126 MGI PMID:33681192 1621479 4933425B07Rik RIKEN cDNA 4933425B07 gene gene MP:0001948 vesicoureteral reflux IAGP N RGD:5509061 20230126 MGI PMID:33681192 1621479 4933425B07Rik RIKEN cDNA 4933425B07 gene gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20230126 MGI PMID:33681192 1621479 4933425B07Rik RIKEN cDNA 4933425B07 gene gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20230126 MGI PMID:33681192 1621479 4933425B07Rik RIKEN cDNA 4933425B07 gene gene MP:0004017 duplex kidney IAGP N RGD:5509061 20230126 MGI PMID:33681192 1621479 4933425B07Rik RIKEN cDNA 4933425B07 gene gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20230126 MGI PMID:33681192 1621479 4933425B07Rik RIKEN cDNA 4933425B07 gene gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20230126 MGI PMID:33681192 1621479 4933425B07Rik RIKEN cDNA 4933425B07 gene gene MP:0011457 abnormal metanephric ureteric bud development IAGP N RGD:5509061 20230126 MGI PMID:33681192 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0000692 small spleen IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20200310 MGI PMID:29539633 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0001925 male infertility IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0002083 premature death IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0002766 situs inversus IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0002767 situs ambiguus IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0003178 left pulmonary isomerism IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0003414 epidermal cyst IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:29539633 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0008923 thoracoschisis IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0010406 common atrium IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0010427 double outlet left ventricle IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0010434 double inlet heart right ventricle IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0010440 anomalous pulmonary venous connection IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0010490 abnormal inferior vena cava valve morphology IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0010912 herniated liver IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:29539633 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0011250 abdominal situs ambiguus IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0011252 situs inversus totalis IAGP N RGD:5509061 20210805 MGI PMID:34124066 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0013247 placenta necrosis IAGP N RGD:5509061 20200310 MGI PMID:29539633 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0013830 abnormal intrathoracic topology of vagus nerve IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0013843 hepatic portal vein stenosis IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0013847 retropleural edema IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0013858 abnormal azygos vein topology IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0013868 abnormal ventral pancreas topology IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0013936 abnormal thymus topology IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0013977 symmetric azygos veins IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0013982 inverse situs of great intrathoracic arteries IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0013987 absent intrahepatic inferior vena cava segment IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0020491 abnormal ovary topology IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0020492 abnormal superior mesenteric vein topology IEA N RGD:5509061 20200310 MGI 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:29539633 1621480 Cfap53 cilia and flagella associated protein 53 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20220428 MGI PMID:34124066 1621482 Clvs1 clavesin 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20221215 MGI 1621482 Clvs1 clavesin 1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20170105 MGI 1621482 Clvs1 clavesin 1 gene MP:0003064 decreased coping response IEA N RGD:5509061 20210128 MGI 1621482 Clvs1 clavesin 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1621482 Clvs1 clavesin 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1621485 Plpp6 phospholipid phosphatase 6 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20181227 MGI 1621485 Plpp6 phospholipid phosphatase 6 gene MP:0001148 enlarged testis IEA N RGD:5509061 20181227 MGI 1621485 Plpp6 phospholipid phosphatase 6 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20221215 MGI 1621487 Terb2 telomere repeat binding bouquet formation protein 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20191024 MGI PMID:30718482 1621487 Terb2 telomere repeat binding bouquet formation protein 2 gene MP:0001147 small testis IAGP N RGD:5509061 20191024 MGI PMID:30718482 1621487 Terb2 telomere repeat binding bouquet formation protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20191024 MGI PMID:30718482 1621487 Terb2 telomere repeat binding bouquet formation protein 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20191024 MGI PMID:30718482 1621487 Terb2 telomere repeat binding bouquet formation protein 2 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20191024 MGI PMID:30718482 1621487 Terb2 telomere repeat binding bouquet formation protein 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20191024 MGI PMID:30718482 1621487 Terb2 telomere repeat binding bouquet formation protein 2 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20191024 MGI PMID:30718482 1621487 Terb2 telomere repeat binding bouquet formation protein 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20191024 MGI PMID:30718482 1621487 Terb2 telomere repeat binding bouquet formation protein 2 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20191024 MGI PMID:30718482 1621487 Terb2 telomere repeat binding bouquet formation protein 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20191024 MGI PMID:30718482 1621487 Terb2 telomere repeat binding bouquet formation protein 2 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20191024 MGI PMID:30718482 1621487 Terb2 telomere repeat binding bouquet formation protein 2 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20191024 MGI PMID:30718482 1621487 Terb2 telomere repeat binding bouquet formation protein 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20191024 MGI PMID:30718482 1621489 Otud3 OTU domain containing 3 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20201029 MGI PMID:32679077 1621489 Otud3 OTU domain containing 3 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20201029 MGI PMID:32679077 1621489 Otud3 OTU domain containing 3 gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20201029 MGI PMID:32679077 1621489 Otud3 OTU domain containing 3 gene MP:0031023 decreased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20201224 MGI PMID:32679077 1621492 Tgfbrap1 transforming growth factor, beta receptor associated protein 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20211104 MGI PMID:20961651 1621492 Tgfbrap1 transforming growth factor, beta receptor associated protein 1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20211104 MGI PMID:20961651 1621493 Rflna refilin A gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0000139 absent vertebral transverse processes IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0000160 kyphosis IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0000161 scoliosis IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0001255 decreased body height IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0001258 decreased body length IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0001265 decreased body size IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0002764 short tibia IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0003109 short femur IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0004600 abnormal vertebral transverse process morphology IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0004606 absent vertebral spinous process IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0004610 small vertebrae IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0004682 small intervertebral disk IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0004684 intervertebral disk degeneration IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0005227 abnormal vertebral body development IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0006392 abnormal nucleus pulposus morphology IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20151008 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20171221 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0014107 premature chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:24436304 1621493 Rflna refilin A gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:24436304 1621495 Prss57 serine protease 57 gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20210415 MGI PMID:33214666 1621495 Prss57 serine protease 57 gene MP:0000362 decreased mast cell histamine storage IAGP N RGD:5509061 20210415 MGI PMID:33214666 1621495 Prss57 serine protease 57 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 1621495 Prss57 serine protease 57 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 1621495 Prss57 serine protease 57 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1621495 Prss57 serine protease 57 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20210415 MGI PMID:33214666 1621495 Prss57 serine protease 57 gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20210415 MGI PMID:33214666 1621495 Prss57 serine protease 57 gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20220519 MGI 1621495 Prss57 serine protease 57 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20220519 MGI 1621495 Prss57 serine protease 57 gene MP:0009709 hydrometra IEA N RGD:5509061 20210826 MGI 1621495 Prss57 serine protease 57 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20210415 MGI PMID:33214666 1621495 Prss57 serine protease 57 gene MP:0011047 increased lung tissue damping IEA N RGD:5509061 20231207 MGI 1621495 Prss57 serine protease 57 gene MP:0030756 decreased histamine level IAGP N RGD:5509061 20210415 MGI PMID:33214666 1621498 Cenpu centromere protein U gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23724000 1621498 Cenpu centromere protein U gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23724000 1621498 Cenpu centromere protein U gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:23724000 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0000440 domed cranium IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0001925 male infertility IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0002083 premature death IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0008933 abnormal motile primary cilium physiology IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0010854 lung situs inversus IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0011252 situs inversus totalis IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0013858 abnormal azygos vein topology IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621500 Cfap45 cilia and flagella associated protein 45 gene MP:0020494 left sided inferior vena cava IAGP N RGD:5509061 20210408 MGI PMID:33139725 1621501 Fam217a family with sequence similarity 217, member A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1621502 Tex44 testis expressed 44 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20241107 MGI PMID:38750428 1621502 Tex44 testis expressed 44 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20241107 MGI PMID:38750428 1621502 Tex44 testis expressed 44 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20241107 MGI PMID:38750428 1621502 Tex44 testis expressed 44 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20241107 MGI PMID:38750428 1621502 Tex44 testis expressed 44 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20241107 MGI PMID:38750428 1621502 Tex44 testis expressed 44 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20241107 MGI PMID:38750428 1621502 Tex44 testis expressed 44 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20241107 MGI PMID:38750428 1621502 Tex44 testis expressed 44 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20241107 MGI PMID:38750428 1621502 Tex44 testis expressed 44 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20241107 MGI PMID:38750428 1621502 Tex44 testis expressed 44 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20241107 MGI PMID:38750428 1621502 Tex44 testis expressed 44 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20241107 MGI PMID:38750428 1621502 Tex44 testis expressed 44 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20241107 MGI PMID:38750428 1621502 Tex44 testis expressed 44 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20241107 MGI PMID:38750428 1621502 Tex44 testis expressed 44 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20241107 MGI PMID:38750428 1621503 Cfap52 cilia and flagella associated protein 52 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20240905 MGI PMID:37236356 1621503 Cfap52 cilia and flagella associated protein 52 gene MP:0001925 male infertility IAGP N RGD:5509061 20240905 MGI PMID:37236356 1621503 Cfap52 cilia and flagella associated protein 52 gene MP:0002083 premature death IAGP N RGD:5509061 20240905 MGI PMID:37236356 1621503 Cfap52 cilia and flagella associated protein 52 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20240905 MGI PMID:37236356 1621503 Cfap52 cilia and flagella associated protein 52 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20240905 MGI PMID:37236356 1621503 Cfap52 cilia and flagella associated protein 52 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20240905 MGI PMID:37236356 1621503 Cfap52 cilia and flagella associated protein 52 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20240905 MGI PMID:37236356 1621505 Tcp11x2 t-complex 11 family, X-linked 2 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 1621507 Csl citrate synthase like gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20201015 MGI PMID:31857692 1621507 Csl citrate synthase like gene MP:0001935 decreased litter size IAGP N RGD:5509061 20201015 MGI PMID:31857692 1621507 Csl citrate synthase like gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20201015 MGI PMID:31857692 1621507 Csl citrate synthase like gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20201015 MGI PMID:31857692 1621507 Csl citrate synthase like gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20201015 MGI PMID:31857692 1621507 Csl citrate synthase like gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20201015 MGI PMID:31857692 1621507 Csl citrate synthase like gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20201015 MGI PMID:31857692 1621507 Csl citrate synthase like gene MP:0031013 abnormal egg activation IAGP N RGD:5509061 20201015 MGI PMID:31857692 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20210128 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210520 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210128 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210520 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20240523 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210520 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0009454 impaired contextual conditioning behavior IEA N RGD:5509061 20201022 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0009456 impaired cued conditioning behavior IEA N RGD:5509061 20220519 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 1621510 Slc25a18 solute carrier family 25 (mitochondrial carrier), member 18 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1621511 Filip1 filamin A interacting protein 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20240307 MGI PMID:26655467 1621511 Filip1 filamin A interacting protein 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20240307 MGI PMID:26655467 1621511 Filip1 filamin A interacting protein 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20240307 MGI PMID:25220605 1621511 Filip1 filamin A interacting protein 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20240307 MGI PMID:25220605 1621511 Filip1 filamin A interacting protein 1 gene MP:0020511 decreased dendritic spine length IAGP N RGD:5509061 20240307 MGI PMID:25220605 1621512 Tbccd1 TBCC domain containing 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1621512 Tbccd1 TBCC domain containing 1 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1621512 Tbccd1 TBCC domain containing 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1621512 Tbccd1 TBCC domain containing 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1621513 Tcerg1l transcription elongation regulator 1-like gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 1621514 Tln2 talin 2 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:22925892 1621514 Tln2 talin 2 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20111116 MGI 1621514 Tln2 talin 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:19793892 1621514 Tln2 talin 2 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19793892 1621514 Tln2 talin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16202389 1621514 Tln2 talin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19220457 1621514 Tln2 talin 2 gene MP:0003939 abnormal myotome morphology IAGP N RGD:5509061 20141003 MGI PMID:19793892 1621514 Tln2 talin 2 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:19793892 1621514 Tln2 talin 2 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20180531 MGI PMID:19793892 1621514 Tln2 talin 2 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:19793892 1621514 Tln2 talin 2 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:19793892 1621514 Tln2 talin 2 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:22925892 1621514 Tln2 talin 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20230601 MGI PMID:35243414 1621514 Tln2 talin 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19793892 1621514 Tln2 talin 2 gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20230601 MGI PMID:35243414 1621514 Tln2 talin 2 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22925892 1621514 Tln2 talin 2 gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20161013 MGI PMID:19793892 1621514 Tln2 talin 2 gene MP:0030959 abnormal myoblast fusion IAGP N RGD:5509061 20190725 MGI PMID:19793892 1621515 Eef2kmt eukaryotic elongation factor 2 lysine methyltransferase gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 1621515 Eef2kmt eukaryotic elongation factor 2 lysine methyltransferase gene MP:0005573 increased pulmonary respiratory rate IEA N RGD:5509061 20220811 MGI 1621516 Ddo D-aspartate oxidase gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16525061 1621516 Ddo D-aspartate oxidase gene MP:0001377 abnormal mating frequency IAGP N RGD:5509061 20141003 MGI PMID:16525061 1621516 Ddo D-aspartate oxidase gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:16525061 1621516 Ddo D-aspartate oxidase gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:16525061 1621516 Ddo D-aspartate oxidase gene MP:0009856 failure of ejaculation IAGP N RGD:5509061 20141003 MGI PMID:16525061 1621516 Ddo D-aspartate oxidase gene MP:0030742 increased aspartic acid level IAGP N RGD:5509061 20180927 MGI PMID:16516413 1621516 Ddo D-aspartate oxidase gene MP:0030742 increased aspartic acid level IAGP N RGD:5509061 20180927 MGI PMID:16525061 1621517 Glipr1l1 GLI pathogenesis-related 1 like 1 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20231116 MGI PMID:31672133 1621517 Glipr1l1 GLI pathogenesis-related 1 like 1 gene MP:0031009 abnormal sperm-egg fusion IAGP N RGD:5509061 20231116 MGI PMID:31672133 1621520 Scnm1 sodium channel modifier 1 gene MP:0000745 tremors IAGP N RGD:5509061 20181220 MGI PMID:12204355 1621520 Scnm1 sodium channel modifier 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:18791226 1621520 Scnm1 sodium channel modifier 1 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:12374766 1621520 Scnm1 sodium channel modifier 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:18791226 1621520 Scnm1 sodium channel modifier 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18791226 1621520 Scnm1 sodium channel modifier 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12374766 1621520 Scnm1 sodium channel modifier 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20181220 MGI PMID:12204355 1621520 Scnm1 sodium channel modifier 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18791226 1621520 Scnm1 sodium channel modifier 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12374766 1621520 Scnm1 sodium channel modifier 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18791226 1621520 Scnm1 sodium channel modifier 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18791226 1621520 Scnm1 sodium channel modifier 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20181220 MGI PMID:12204355 1621520 Scnm1 sodium channel modifier 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:12374766 1621520 Scnm1 sodium channel modifier 1 gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20181220 MGI PMID:12204355 1621520 Scnm1 sodium channel modifier 1 gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:12374766 1621520 Scnm1 sodium channel modifier 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20181220 MGI PMID:12204355 1621520 Scnm1 sodium channel modifier 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18791226 1621520 Scnm1 sodium channel modifier 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20181220 MGI PMID:12204355 1621520 Scnm1 sodium channel modifier 1 gene MP:0009434 paraparesis IAGP N RGD:5509061 20181220 MGI PMID:12204355 1621523 Svbp small vasohibin binding protein gene MP:0000433 microcephaly IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0000774 decreased brain size IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0000774 decreased brain size IAGP N RGD:5509061 20220707 MGI PMID:35482892 1621523 Svbp small vasohibin binding protein gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0000852 small cerebellum IAGP N RGD:5509061 20220707 MGI PMID:35482892 1621523 Svbp small vasohibin binding protein gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0001399 hyperactivity IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20220707 MGI PMID:35482892 1621523 Svbp small vasohibin binding protein gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20220707 MGI PMID:35482892 1621523 Svbp small vasohibin binding protein gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0012466 decreased hippocampal fimbria size IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20220707 MGI PMID:35482892 1621523 Svbp small vasohibin binding protein gene MP:0020527 small thalamus IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621523 Svbp small vasohibin binding protein gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20220707 MGI PMID:31363758 1621525 Retreg3 reticulophagy regulator family member 3 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1621525 Retreg3 reticulophagy regulator family member 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1621525 Retreg3 reticulophagy regulator family member 3 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20201022 MGI 1621525 Retreg3 reticulophagy regulator family member 3 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20141003 MGI 1621525 Retreg3 reticulophagy regulator family member 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1621525 Retreg3 reticulophagy regulator family member 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 1621525 Retreg3 reticulophagy regulator family member 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1621525 Retreg3 reticulophagy regulator family member 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20240523 MGI 1621525 Retreg3 reticulophagy regulator family member 3 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1621525 Retreg3 reticulophagy regulator family member 3 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20210128 MGI 1621525 Retreg3 reticulophagy regulator family member 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1621526 Tmx3 thioredoxin-related transmembrane protein 3 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20231109 MGI PMID:36325906 1621526 Tmx3 thioredoxin-related transmembrane protein 3 gene MP:0008823 abnormal interventricular septum membranous part morphology IAGP N RGD:5509061 20231109 MGI PMID:36325906 1621526 Tmx3 thioredoxin-related transmembrane protein 3 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20231109 MGI PMID:36325906 1621526 Tmx3 thioredoxin-related transmembrane protein 3 gene MP:0010498 abnormal interventricular septum muscular part morphology IAGP N RGD:5509061 20231109 MGI PMID:36325906 1621529 Hormad1 HORMA domain containing 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:21478856 1621529 Hormad1 HORMA domain containing 1 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:21478856 1621529 Hormad1 HORMA domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:22530760 1621529 Hormad1 HORMA domain containing 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:21478856 1621529 Hormad1 HORMA domain containing 1 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20200310 MGI PMID:22530760 1621529 Hormad1 HORMA domain containing 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20200310 MGI PMID:22530760 1621529 Hormad1 HORMA domain containing 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:22530760 1621529 Hormad1 HORMA domain containing 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:21478856 1621529 Hormad1 HORMA domain containing 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:22530760 1621529 Hormad1 HORMA domain containing 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20200310 MGI PMID:21478856 1621529 Hormad1 HORMA domain containing 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20200310 MGI PMID:22530760 1621529 Hormad1 HORMA domain containing 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20200310 MGI PMID:21478856 1621529 Hormad1 HORMA domain containing 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20200310 MGI PMID:22530760 1621529 Hormad1 HORMA domain containing 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20201015 MGI PMID:32345962 1621529 Hormad1 HORMA domain containing 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20200310 MGI PMID:22530760 1621529 Hormad1 HORMA domain containing 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20200310 MGI PMID:22530760 1621529 Hormad1 HORMA domain containing 1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:21478856 1621529 Hormad1 HORMA domain containing 1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:22530760 1621529 Hormad1 HORMA domain containing 1 gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20200310 MGI PMID:21478856 1621529 Hormad1 HORMA domain containing 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20200310 MGI PMID:22530760 1621529 Hormad1 HORMA domain containing 1 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20200310 MGI PMID:21478856 1621529 Hormad1 HORMA domain containing 1 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20200310 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20200310 MGI PMID:21478856 1621529 Hormad1 HORMA domain containing 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0014443 impaired polar body extrusion IAGP N RGD:5509061 20240509 MGI PMID:21478856 1621529 Hormad1 HORMA domain containing 1 gene MP:0014445 abnormal spindle assembly in female meiosis IAGP N RGD:5509061 20240509 MGI PMID:21079677 1621529 Hormad1 HORMA domain containing 1 gene MP:0014445 abnormal spindle assembly in female meiosis IAGP N RGD:5509061 20240509 MGI PMID:21478856 1621531 Rps27l ribosomal protein S27-like gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0000599 enlarged liver IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0000601 small liver IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0001265 decreased body size IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0002083 premature death IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240808 MGI PMID:37306301 1621531 Rps27l ribosomal protein S27-like gene MP:0004024 aneuploidy IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621531 Rps27l ribosomal protein S27-like gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20240808 MGI PMID:37306301 1621531 Rps27l ribosomal protein S27-like gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160225 MGI PMID:25144937 1621536 Zcchc3 zinc finger, CCHC domain containing 3 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20200409 MGI PMID:30135424 1621536 Zcchc3 zinc finger, CCHC domain containing 3 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 1621536 Zcchc3 zinc finger, CCHC domain containing 3 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1621536 Zcchc3 zinc finger, CCHC domain containing 3 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20200409 MGI PMID:30135424 1621536 Zcchc3 zinc finger, CCHC domain containing 3 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20200409 MGI PMID:30135424 1621536 Zcchc3 zinc finger, CCHC domain containing 3 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:30135424 1621536 Zcchc3 zinc finger, CCHC domain containing 3 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:30135424 1621536 Zcchc3 zinc finger, CCHC domain containing 3 gene MP:0031034 increased susceptibility to Poxviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:30135424 1621536 Zcchc3 zinc finger, CCHC domain containing 3 gene MP:0031219 decreased circulating CXCL10 level IAGP N RGD:5509061 20210204 MGI PMID:30135424 1621538 Ppm1m protein phosphatase 1M gene MP:0012361 decreased large unstained cell number IEA N RGD:5509061 20210128 MGI 1621541 Mtfp1 mitochondrial fission process 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20240307 MGI PMID:36333300 1621541 Mtfp1 mitochondrial fission process 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20240307 MGI PMID:36333300 1621541 Mtfp1 mitochondrial fission process 1 gene MP:0002083 premature death IAGP N RGD:5509061 20240307 MGI PMID:36333300 1621541 Mtfp1 mitochondrial fission process 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20240307 MGI PMID:36333300 1621541 Mtfp1 mitochondrial fission process 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20240307 MGI PMID:36333300 1621541 Mtfp1 mitochondrial fission process 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20240307 MGI PMID:36333300 1621541 Mtfp1 mitochondrial fission process 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20240307 MGI PMID:36333300 1621541 Mtfp1 mitochondrial fission process 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20240307 MGI PMID:36333300 1621541 Mtfp1 mitochondrial fission process 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20240307 MGI PMID:36333300 1621541 Mtfp1 mitochondrial fission process 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20240307 MGI PMID:36333300 1621541 Mtfp1 mitochondrial fission process 1 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20240307 MGI PMID:36333300 1621541 Mtfp1 mitochondrial fission process 1 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20240307 MGI PMID:36333300 1621541 Mtfp1 mitochondrial fission process 1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:36333300 1621543 Tmem41a transmembrane protein 41a gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1621545 Tex12 testis expressed 12 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:18611960 1621545 Tex12 testis expressed 12 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18611960 1621545 Tex12 testis expressed 12 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18611960 1621545 Tex12 testis expressed 12 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18611960 1621545 Tex12 testis expressed 12 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:18611960 1621545 Tex12 testis expressed 12 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:18611960 1621545 Tex12 testis expressed 12 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18611960 1621545 Tex12 testis expressed 12 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:18611960 1621545 Tex12 testis expressed 12 gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20141003 MGI PMID:18611960 1621545 Tex12 testis expressed 12 gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20220407 MGI PMID:18611960 1621545 Tex12 testis expressed 12 gene MP:0011122 absent primordial ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:18611960 1621546 Thg1l tRNA-histidine guanylyltransferase 1-like (S. cerevisiae) gene MP:0009476 enlarged cecum IEA N RGD:5509061 20181227 MGI 1621546 Thg1l tRNA-histidine guanylyltransferase 1-like (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1621547 Snx9 sorting nexin 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20211216 MGI PMID:27655699 1621550 Mlxipl MLX interacting protein-like gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0001263 weight loss IAGP N RGD:5509061 20190523 MGI PMID:29669261 1621550 Mlxipl MLX interacting protein-like gene MP:0001668 abnormal intestinal fructose absorption IAGP N RGD:5509061 20190523 MGI PMID:29669261 1621550 Mlxipl MLX interacting protein-like gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0001925 male infertility IAGP N RGD:5509061 20230330 MGI PMID:34669700 1621550 Mlxipl MLX interacting protein-like gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0002083 premature death IAGP N RGD:5509061 20190523 MGI PMID:29669261 1621550 Mlxipl MLX interacting protein-like gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20190523 MGI PMID:29669261 1621550 Mlxipl MLX interacting protein-like gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230330 MGI PMID:34669700 1621550 Mlxipl MLX interacting protein-like gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0005036 diarrhea IAGP N RGD:5509061 20190523 MGI PMID:29669261 1621550 Mlxipl MLX interacting protein-like gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20190523 MGI PMID:29669261 1621550 Mlxipl MLX interacting protein-like gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20190523 MGI PMID:29669261 1621550 Mlxipl MLX interacting protein-like gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20190523 MGI PMID:29669261 1621550 Mlxipl MLX interacting protein-like gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20190523 MGI PMID:29669261 1621550 Mlxipl MLX interacting protein-like gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20190523 MGI PMID:29669261 1621550 Mlxipl MLX interacting protein-like gene MP:0009480 distended cecum IAGP N RGD:5509061 20190523 MGI PMID:29669261 1621550 Mlxipl MLX interacting protein-like gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:15118080 1621550 Mlxipl MLX interacting protein-like gene MP:0011940 decreased food intake IAGP N RGD:5509061 20190523 MGI PMID:29669261 1621550 Mlxipl MLX interacting protein-like gene MP:0012311 decreased defecation amount IAGP N RGD:5509061 20190523 MGI PMID:29669261 1621550 Mlxipl MLX interacting protein-like gene MP:0013955 increased colon length IAGP N RGD:5509061 20190523 MGI PMID:29669261 1621550 Mlxipl MLX interacting protein-like gene MP:0020869 immotile sperm IAGP N RGD:5509061 20230330 MGI PMID:34669700 1621550 Mlxipl MLX interacting protein-like gene MP:0031236 increased cecum weight IAGP N RGD:5509061 20210610 MGI PMID:29669261 1621551 Pmaip1 phorbol-12-myristate-13-acetate-induced protein 1 gene MP:0003010 decreased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12952892 1621551 Pmaip1 phorbol-12-myristate-13-acetate-induced protein 1 gene MP:0004587 decreased cellular sensitivity to X-ray irradiation IAGP N RGD:5509061 20141003 MGI PMID:12952892 1621551 Pmaip1 phorbol-12-myristate-13-acetate-induced protein 1 gene MP:0005068 abnormal NK cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17618288 1621551 Pmaip1 phorbol-12-myristate-13-acetate-induced protein 1 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:12952892 1621551 Pmaip1 phorbol-12-myristate-13-acetate-induced protein 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:12952892 1621551 Pmaip1 phorbol-12-myristate-13-acetate-induced protein 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:14500851 1621552 Fkbpl FK506 binding protein-like gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20160602 MGI PMID:25767277 1621552 Fkbpl FK506 binding protein-like gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20160602 MGI PMID:25767277 1621552 Fkbpl FK506 binding protein-like gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20160602 MGI PMID:25767277 1621552 Fkbpl FK506 binding protein-like gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20160602 MGI PMID:25767277 1621552 Fkbpl FK506 binding protein-like gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20160602 MGI PMID:25767277 1621552 Fkbpl FK506 binding protein-like gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20160602 MGI PMID:25767277 1621552 Fkbpl FK506 binding protein-like gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160602 MGI PMID:25767277 1621552 Fkbpl FK506 binding protein-like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1621552 Fkbpl FK506 binding protein-like gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20160602 MGI PMID:25767277 1621552 Fkbpl FK506 binding protein-like gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1621552 Fkbpl FK506 binding protein-like gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20890045 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15665283 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15665283 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16135822 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16135822 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16135822 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20890045 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20160811 MGI PMID:26980762 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20160811 MGI PMID:26980762 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:16135822 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:20890045 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:20890045 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15665283 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:16135822 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20160811 MGI PMID:26980762 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16135822 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20160811 MGI PMID:26980762 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0010040 abnormal oval cell morphology IAGP N RGD:5509061 20160811 MGI PMID:26980762 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0010054 increased hepatoblastoma incidence IAGP N RGD:5509061 20160811 MGI PMID:26980762 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16135822 1621553 Rassf1 Ras association (RalGDS/AF-6) domain family member 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16135822 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0000088 short mandible IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20201022 MGI 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0000445 short snout IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20201022 MGI 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0001407 short stride length IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0002083 premature death IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0003908 decreased stereotypic behavior IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0006276 abnormal autonomic nervous system physiology IAGP N RGD:5509061 20240321 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20240321 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0014114 abnormal cognition IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0021090 abnormal dendrite arborization pattern IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621555 Hnrnph2 heterogeneous nuclear ribonucleoprotein H2 gene MP:0021112 impaired social recognition IAGP N RGD:5509061 20240215 MGI PMID:37463454 1621556 Tspan5 tetraspanin 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1621557 Htra1 HtrA serine peptidase 1 gene MP:0003279 aneurysm IAGP N RGD:5509061 20200310 MGI PMID:21844367 1621557 Htra1 HtrA serine peptidase 1 gene MP:0005098 abnormal optic choroid morphology IAGP N RGD:5509061 20200310 MGI PMID:21844367 1621557 Htra1 HtrA serine peptidase 1 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20200310 MGI PMID:24040176 1621557 Htra1 HtrA serine peptidase 1 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20200310 MGI PMID:24040176 1621558 Krt35 keratin 35 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1621558 Krt35 keratin 35 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20230601 MGI 1621558 Krt35 keratin 35 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12861006 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0000960 abnormal sensory ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12861006 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12861006 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0002830 gallstones IAGP N RGD:5509061 20141003 MGI PMID:12861006 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:12861006 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:12861006 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0004267 abnormal optic tract morphology IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0004298 vestibular ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0006409 vestibular ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0008492 dorsal root ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0009342 enlarged gallbladder IAGP N RGD:5509061 20141003 MGI PMID:12861006 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:21262811 1621559 Vti1b vesicle transport through interaction with t-SNAREs 1B gene MP:0020548 decreased optic chiasm size IAGP N RGD:5509061 20180301 MGI PMID:21262811 1621562 Tslp thymic stromal lymphopoietin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21820333 1621562 Tslp thymic stromal lymphopoietin gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:22585305 1621562 Tslp thymic stromal lymphopoietin gene MP:0002334 abnormal airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:22585305 1621562 Tslp thymic stromal lymphopoietin gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:22585305 1621562 Tslp thymic stromal lymphopoietin gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:22585305 1621562 Tslp thymic stromal lymphopoietin gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:18650845 1621562 Tslp thymic stromal lymphopoietin gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:21820333 1621562 Tslp thymic stromal lymphopoietin gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18650845 1621562 Tslp thymic stromal lymphopoietin gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18650845 1621562 Tslp thymic stromal lymphopoietin gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:22585305 1621562 Tslp thymic stromal lymphopoietin gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:23437132 1621562 Tslp thymic stromal lymphopoietin gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22585305 1621562 Tslp thymic stromal lymphopoietin gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22585305 1621562 Tslp thymic stromal lymphopoietin gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:23437132 1621562 Tslp thymic stromal lymphopoietin gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:22585305 1621562 Tslp thymic stromal lymphopoietin gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:23437132 1621562 Tslp thymic stromal lymphopoietin gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:23437132 1621562 Tslp thymic stromal lymphopoietin gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18650845 1621562 Tslp thymic stromal lymphopoietin gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21820333 1621563 Macir macrophage immunometabolism regulator gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220519 MGI 1621563 Macir macrophage immunometabolism regulator gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20210520 MGI 1621563 Macir macrophage immunometabolism regulator gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 1621563 Macir macrophage immunometabolism regulator gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1621563 Macir macrophage immunometabolism regulator gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1621563 Macir macrophage immunometabolism regulator gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1621564 D6Ertd527e DNA segment, Chr 6, ERATO Doi 527, expressed gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20231109 MGI PMID:36482406 1621564 D6Ertd527e DNA segment, Chr 6, ERATO Doi 527, expressed gene MP:0001935 decreased litter size IAGP N RGD:5509061 20231109 MGI PMID:36482406 1621565 Wwc2 WW, C2 and coiled-coil domain containing 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210603 MGI PMID:29116649 1621565 Wwc2 WW, C2 and coiled-coil domain containing 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20210603 MGI PMID:29116649 1621565 Wwc2 WW, C2 and coiled-coil domain containing 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20210603 MGI PMID:29116649 1621565 Wwc2 WW, C2 and coiled-coil domain containing 2 gene MP:0001925 male infertility IEA N RGD:5509061 20240523 MGI 1621565 Wwc2 WW, C2 and coiled-coil domain containing 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20210603 MGI PMID:29116649 1621565 Wwc2 WW, C2 and coiled-coil domain containing 2 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20210603 MGI PMID:29116649 1621565 Wwc2 WW, C2 and coiled-coil domain containing 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 1621565 Wwc2 WW, C2 and coiled-coil domain containing 2 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20210603 MGI PMID:29116649 1621565 Wwc2 WW, C2 and coiled-coil domain containing 2 gene MP:0008993 abnormal portal triad morphology IAGP N RGD:5509061 20210603 MGI PMID:29116649 1621565 Wwc2 WW, C2 and coiled-coil domain containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1621565 Wwc2 WW, C2 and coiled-coil domain containing 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1621565 Wwc2 WW, C2 and coiled-coil domain containing 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20231207 MGI 1621566 Atxn1l ataxin 1-like gene MP:0000160 kyphosis IAGP N RGD:5509061 20200310 MGI PMID:22014525 1621566 Atxn1l ataxin 1-like gene MP:0000440 domed cranium IAGP N RGD:5509061 20200310 MGI PMID:22014525 1621566 Atxn1l ataxin 1-like gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:22014525 1621566 Atxn1l ataxin 1-like gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20200310 MGI PMID:28288114 1621566 Atxn1l ataxin 1-like gene MP:0001575 cyanosis IAGP N RGD:5509061 20200310 MGI PMID:22014525 1621566 Atxn1l ataxin 1-like gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200310 MGI PMID:22014525 1621566 Atxn1l ataxin 1-like gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:17322884 1621566 Atxn1l ataxin 1-like gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20200310 MGI PMID:22014525 1621566 Atxn1l ataxin 1-like gene MP:0003052 omphalocele IAGP N RGD:5509061 20200310 MGI PMID:22014525 1621566 Atxn1l ataxin 1-like gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:17322884 1621566 Atxn1l ataxin 1-like gene MP:0005150 cachexia IAGP N RGD:5509061 20200310 MGI PMID:22014525 1621566 Atxn1l ataxin 1-like gene MP:0005202 lethargy IAGP N RGD:5509061 20200310 MGI PMID:22014525 1621566 Atxn1l ataxin 1-like gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20200310 MGI PMID:28288114 1621566 Atxn1l ataxin 1-like gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20200310 MGI PMID:22014525 1621566 Atxn1l ataxin 1-like gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20200310 MGI PMID:22014525 1621566 Atxn1l ataxin 1-like gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20200310 MGI PMID:17322884 1621566 Atxn1l ataxin 1-like gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20200310 MGI PMID:28288114 1621566 Atxn1l ataxin 1-like gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20200310 MGI PMID:22014525 1621566 Atxn1l ataxin 1-like gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22014525 1621566 Atxn1l ataxin 1-like gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22014525 1621566 Atxn1l ataxin 1-like gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22014525 1621566 Atxn1l ataxin 1-like gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20200310 MGI PMID:28288114 1621566 Atxn1l ataxin 1-like gene MP:0020594 decreased cerebral cortex cell number IAGP N RGD:5509061 20200310 MGI PMID:28288114 1621566 Atxn1l ataxin 1-like gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:28288114 1621568 Snf8 SNF8, ESCRT-II complex subunit, homolog (S. cerevisiae) gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20200310 MGI 1621569 Nelfe negative elongation factor complex member E, Rdbp gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1621569 Nelfe negative elongation factor complex member E, Rdbp gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1621571 Gnpda1 glucosamine-6-phosphate deaminase 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1621571 Gnpda1 glucosamine-6-phosphate deaminase 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 1621571 Gnpda1 glucosamine-6-phosphate deaminase 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1621571 Gnpda1 glucosamine-6-phosphate deaminase 1 gene MP:0002989 small kidney IEA N RGD:5509061 20160811 MGI 1621571 Gnpda1 glucosamine-6-phosphate deaminase 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1621571 Gnpda1 glucosamine-6-phosphate deaminase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1621571 Gnpda1 glucosamine-6-phosphate deaminase 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20151015 MGI PMID:25144618 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:21103374 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:21103374 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:21103374 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001258 decreased body length IAGP N RGD:5509061 20151015 MGI PMID:25144618 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001260 increased body weight IAGP N RGD:5509061 20151015 MGI PMID:25144618 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21103374 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23300482 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001399 hyperactivity IEA N RGD:5509061 20160804 MGI 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20151015 MGI PMID:25144618 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:21103374 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21103374 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23300482 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20151015 MGI PMID:25144618 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20151015 MGI PMID:25144618 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:21103374 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23300482 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20160804 MGI 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:21103374 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:21103374 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21103374 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:23300482 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23300482 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005331 insulin resistance IAGP N RGD:5509061 20151015 MGI PMID:25144618 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20151015 MGI PMID:25144618 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005571 decreased lactate dehydrogenase level IEA N RGD:5509061 20160804 MGI 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:21103374 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005662 increased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20151015 MGI PMID:25144618 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0008962 abnormal carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:21103374 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:23300482 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20151015 MGI PMID:25144618 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20151015 MGI PMID:25144618 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20151015 MGI PMID:25144618 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20151015 MGI PMID:25144618 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21103374 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23300482 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:23300482 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19234441 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21103374 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23300482 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0011478 abnormal urine catecholamine level IAGP N RGD:5509061 20141003 MGI PMID:19680540 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:23300482 1621572 Fto FTO alpha-ketoglutarate dependent dioxygenase gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:23300482 1621573 Esrrb estrogen related receptor, beta gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170810 MGI PMID:28130335 1621573 Esrrb estrogen related receptor, beta gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:17765677 1621573 Esrrb estrogen related receptor, beta gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:17765677 1621573 Esrrb estrogen related receptor, beta gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9285590 1621573 Esrrb estrogen related receptor, beta gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:9285590 1621573 Esrrb estrogen related receptor, beta gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:9285590 1621573 Esrrb estrogen related receptor, beta gene MP:0002083 premature death IAGP N RGD:5509061 20170810 MGI PMID:28130335 1621573 Esrrb estrogen related receptor, beta gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9285590 1621573 Esrrb estrogen related receptor, beta gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:17765677 1621573 Esrrb estrogen related receptor, beta gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20170810 MGI PMID:28130335 1621573 Esrrb estrogen related receptor, beta gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170810 MGI PMID:28130335 1621573 Esrrb estrogen related receptor, beta gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:9285590 1621573 Esrrb estrogen related receptor, beta gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20170810 MGI PMID:28130335 1621573 Esrrb estrogen related receptor, beta gene MP:0003169 abnormal scala media morphology IAGP N RGD:5509061 20141003 MGI PMID:17765677 1621573 Esrrb estrogen related receptor, beta gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:9285590 1621573 Esrrb estrogen related receptor, beta gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9285590 1621573 Esrrb estrogen related receptor, beta gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:9285590 1621573 Esrrb estrogen related receptor, beta gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20170810 MGI PMID:28130335 1621573 Esrrb estrogen related receptor, beta gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20170810 MGI PMID:28130335 1621573 Esrrb estrogen related receptor, beta gene MP:0004758 absent strial marginal cells IAGP N RGD:5509061 20141003 MGI PMID:17765677 1621573 Esrrb estrogen related receptor, beta gene MP:0004887 decreased endolymph production IAGP N RGD:5509061 20141003 MGI PMID:17765677 1621573 Esrrb estrogen related receptor, beta gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9285590 1621573 Esrrb estrogen related receptor, beta gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9285590 1621573 Esrrb estrogen related receptor, beta gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170810 MGI PMID:28130335 1621573 Esrrb estrogen related receptor, beta gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20170810 MGI PMID:28130335 1621573 Esrrb estrogen related receptor, beta gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20170810 MGI PMID:28130335 1621573 Esrrb estrogen related receptor, beta gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17765677 1621573 Esrrb estrogen related receptor, beta gene MP:0008308 small scala media IAGP N RGD:5509061 20141003 MGI PMID:17765677 1621573 Esrrb estrogen related receptor, beta gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20141003 MGI PMID:17765677 1621573 Esrrb estrogen related receptor, beta gene MP:0009593 absent chorion IAGP N RGD:5509061 20141003 MGI PMID:9285590 1621573 Esrrb estrogen related receptor, beta gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:9285590 1621573 Esrrb estrogen related receptor, beta gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17765677 1621573 Esrrb estrogen related receptor, beta gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9285590 1621573 Esrrb estrogen related receptor, beta gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17765677 1621573 Esrrb estrogen related receptor, beta gene MP:0012100 absent spongiotrophoblast IAGP N RGD:5509061 20141003 MGI PMID:9285590 1621573 Esrrb estrogen related receptor, beta gene MP:0012557 decreased calcium uptake by cardiac muscle IAGP N RGD:5509061 20170810 MGI PMID:28130335 1621573 Esrrb estrogen related receptor, beta gene MP:0012558 increased calcium uptake by cardiac muscle IAGP N RGD:5509061 20170810 MGI PMID:28130335 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:20381490 1621574 Ceacam2 CEA cell adhesion molecule 2 gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:20381490 1621575 Ceacam10 CEA cell adhesion molecule 10 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12482980 1621575 Ceacam10 CEA cell adhesion molecule 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12482980 1621581 Xk X-linked Kx blood group gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20170105 MGI 1621581 Xk X-linked Kx blood group gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:23122227 1621581 Xk X-linked Kx blood group gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170105 MGI 1621581 Xk X-linked Kx blood group gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1621581 Xk X-linked Kx blood group gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:24405768 1621581 Xk X-linked Kx blood group gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20170105 MGI 1621581 Xk X-linked Kx blood group gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1621581 Xk X-linked Kx blood group gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:24405768 1621581 Xk X-linked Kx blood group gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20151224 MGI PMID:23122227 1621581 Xk X-linked Kx blood group gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20151224 MGI PMID:23122227 1621581 Xk X-linked Kx blood group gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:24405768 1621581 Xk X-linked Kx blood group gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:24405768 1621581 Xk X-linked Kx blood group gene MP:0010738 abnormal internode morphology IAGP N RGD:5509061 20141003 MGI PMID:24405768 1621581 Xk X-linked Kx blood group gene MP:0011730 increased myelin sheath thickness IAGP N RGD:5509061 20141003 MGI PMID:24405768 1621581 Xk X-linked Kx blood group gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20141003 MGI PMID:24405768 1621581 Xk X-linked Kx blood group gene MP:0011913 abnormal reticulocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23122227 1621581 Xk X-linked Kx blood group gene MP:0012365 increased erythrocyte sodium level IAGP N RGD:5509061 20141003 MGI PMID:23122227 1621581 Xk X-linked Kx blood group gene MP:0012368 increased erythrocyte magnesium level IAGP N RGD:5509061 20141003 MGI PMID:23122227 1621581 Xk X-linked Kx blood group gene MP:0012372 abnormal erythrocyte ion content IAGP N RGD:5509061 20141003 MGI PMID:23122227 1621597 Pde6g phosphodiesterase 6G, cGMP-specific, rod, gamma gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20200310 MGI PMID:8638127 1621597 Pde6g phosphodiesterase 6G, cGMP-specific, rod, gamma gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20200310 MGI PMID:8638127 1621597 Pde6g phosphodiesterase 6G, cGMP-specific, rod, gamma gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20200310 MGI PMID:30573647 1621597 Pde6g phosphodiesterase 6G, cGMP-specific, rod, gamma gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:8638127 1621597 Pde6g phosphodiesterase 6G, cGMP-specific, rod, gamma gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200310 MGI PMID:30573647 1621597 Pde6g phosphodiesterase 6G, cGMP-specific, rod, gamma gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20200310 MGI PMID:8638127 1621597 Pde6g phosphodiesterase 6G, cGMP-specific, rod, gamma gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20200310 MGI PMID:8638127 1621597 Pde6g phosphodiesterase 6G, cGMP-specific, rod, gamma gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200310 MGI PMID:30573647 1621597 Pde6g phosphodiesterase 6G, cGMP-specific, rod, gamma gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20200310 MGI PMID:30573647 1621600 Pcm1 pericentriolar material 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20181227 MGI 1621600 Pcm1 pericentriolar material 1 gene MP:0000692 small spleen IEA N RGD:5509061 20190502 MGI 1621600 Pcm1 pericentriolar material 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20180719 MGI PMID:25697395 1621600 Pcm1 pericentriolar material 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1621600 Pcm1 pericentriolar material 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 1621600 Pcm1 pericentriolar material 1 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20190502 MGI 1621600 Pcm1 pericentriolar material 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1621600 Pcm1 pericentriolar material 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20190502 MGI 1621600 Pcm1 pericentriolar material 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200402 MGI 1621600 Pcm1 pericentriolar material 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20180719 MGI PMID:25697395 1621600 Pcm1 pericentriolar material 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210520 MGI 1621600 Pcm1 pericentriolar material 1 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20210826 MGI 1621600 Pcm1 pericentriolar material 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1621600 Pcm1 pericentriolar material 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1621600 Pcm1 pericentriolar material 1 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20211021 MGI 1621600 Pcm1 pericentriolar material 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210128 MGI 1621600 Pcm1 pericentriolar material 1 gene MP:0020396 abnormal social recognition IAGP N RGD:5509061 20180719 MGI PMID:25697395 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20141003 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:22560297 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22560297 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15169896 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20141003 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0030190 small snout IAGP N RGD:5509061 20171019 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0031447 unilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:21982646 1621601 Pbx2 pre B cell leukemia homeobox 2 gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:21982646 1621602 Pax5 paired box 5 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20150507 MGI 1621602 Pax5 paired box 5 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20181227 MGI 1621602 Pax5 paired box 5 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:23349049 1621602 Pax5 paired box 5 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23349049 1621602 Pax5 paired box 5 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:23349049 1621602 Pax5 paired box 5 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23349049 1621602 Pax5 paired box 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220428 MGI 1621602 Pax5 paired box 5 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20181227 MGI 1621602 Pax5 paired box 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11420047 1621602 Pax5 paired box 5 gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20180215 MGI 1621602 Pax5 paired box 5 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11420047 1621602 Pax5 paired box 5 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8001127 1621602 Pax5 paired box 5 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20170314 MGI PMID:26301816 1621602 Pax5 paired box 5 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11420047 1621602 Pax5 paired box 5 gene MP:0001806 decreased IgM level IEA N RGD:5509061 20150507 MGI 1621602 Pax5 paired box 5 gene MP:0001807 decreased IgA level IEA N RGD:5509061 20150507 MGI 1621602 Pax5 paired box 5 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23349049 1621602 Pax5 paired box 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23349049 1621602 Pax5 paired box 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11420047 1621602 Pax5 paired box 5 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16968900 1621602 Pax5 paired box 5 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9042861 1621602 Pax5 paired box 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11420047 1621602 Pax5 paired box 5 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8001127 1621602 Pax5 paired box 5 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9042861 1621602 Pax5 paired box 5 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17658281 1621602 Pax5 paired box 5 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11420047 1621602 Pax5 paired box 5 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0002491 decreased IgD level IEA N RGD:5509061 20181011 MGI 1621602 Pax5 paired box 5 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:17658281 1621602 Pax5 paired box 5 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1621602 Pax5 paired box 5 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:11420047 1621602 Pax5 paired box 5 gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20180215 MGI 1621602 Pax5 paired box 5 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16968900 1621602 Pax5 paired box 5 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0005020 abnormal late pro-B cell IAGP N RGD:5509061 20141003 MGI PMID:8001127 1621602 Pax5 paired box 5 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1621602 Pax5 paired box 5 gene MP:0005387 immune system phenotype IEA N RGD:5509061 20220811 MGI 1621602 Pax5 paired box 5 gene MP:0005425 increased macrophage cell number IEA N RGD:5509061 20150507 MGI 1621602 Pax5 paired box 5 gene MP:0005432 abnormal pro-B cell morphology IAGP N RGD:5509061 20170314 MGI PMID:26301816 1621602 Pax5 paired box 5 gene MP:0005434 absent late pro-B cells IAGP N RGD:5509061 20141003 MGI PMID:8001127 1621602 Pax5 paired box 5 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0008082 increased single-positive T cell number IEA N RGD:5509061 20150507 MGI 1621602 Pax5 paired box 5 gene MP:0008170 decreased B-1b cell number IEA N RGD:5509061 20180215 MGI 1621602 Pax5 paired box 5 gene MP:0008205 absent B-2 B cells IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11420047 1621602 Pax5 paired box 5 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11420047 1621602 Pax5 paired box 5 gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11420047 1621602 Pax5 paired box 5 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20170314 MGI PMID:26301816 1621602 Pax5 paired box 5 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11420047 1621602 Pax5 paired box 5 gene MP:0008496 decreased IgG2a level IEA N RGD:5509061 20150507 MGI 1621602 Pax5 paired box 5 gene MP:0008497 decreased IgG2b level IEA N RGD:5509061 20150507 MGI 1621602 Pax5 paired box 5 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11420047 1621602 Pax5 paired box 5 gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:18676810 1621602 Pax5 paired box 5 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1621602 Pax5 paired box 5 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20180215 MGI 1621602 Pax5 paired box 5 gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20180215 MGI 1621602 Pax5 paired box 5 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11420047 1621602 Pax5 paired box 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8790871 1621602 Pax5 paired box 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1621602 Pax5 paired box 5 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 1621602 Pax5 paired box 5 gene MP:0013520 increased CD4-positive NK T cell number IEA N RGD:5509061 20211021 MGI 1621602 Pax5 paired box 5 gene MP:0013523 increased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20211021 MGI 1621602 Pax5 paired box 5 gene MP:0014050 increased B cell acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20170314 MGI PMID:26301816 1621602 Pax5 paired box 5 gene MP:0014471 enhanced B cell migration IAGP N RGD:5509061 20240613 MGI PMID:17658281 1621602 Pax5 paired box 5 gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20150507 MGI 1621602 Pax5 paired box 5 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:23349049 1621604 Mest mesoderm specific transcript gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9771709 1621604 Mest mesoderm specific transcript gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:9771709 1621604 Mest mesoderm specific transcript gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:9771709 1621604 Mest mesoderm specific transcript gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9771709 1621604 Mest mesoderm specific transcript gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:12242721 1621604 Mest mesoderm specific transcript gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:12242721 1621604 Mest mesoderm specific transcript gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:9771709 1621604 Mest mesoderm specific transcript gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:9771709 1621604 Mest mesoderm specific transcript gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:9771709 1621604 Mest mesoderm specific transcript gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:9771709 1621604 Mest mesoderm specific transcript gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12242721 1621604 Mest mesoderm specific transcript gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:9771709 1621604 Mest mesoderm specific transcript gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9771709 1621604 Mest mesoderm specific transcript gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9771709 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22354172 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:17597763 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:17597763 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17597763 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24213529 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:22354172 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0003925 abnormal cellular glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:22354172 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22354172 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:17597763 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0005060 accumulation of giant lysosomes in kidney/renal tubule cells IAGP N RGD:5509061 20141003 MGI PMID:17597763 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:17597763 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0008109 abnormal small intestinal microvillus morphology IAGP N RGD:5509061 20141003 MGI PMID:24213529 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0008141 decreased small intestinal microvillus size IAGP N RGD:5509061 20141003 MGI PMID:17597763 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:22354172 1621605 Rab8a RAB8A, member RAS oncogene family gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24213529 1621606 Meg3 maternally expressed 3 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:20610486 1621606 Meg3 maternally expressed 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19264764 1621606 Meg3 maternally expressed 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8903723 1621606 Meg3 maternally expressed 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17014736 1621606 Meg3 maternally expressed 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8903723 1621606 Meg3 maternally expressed 3 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:19264764 1621606 Meg3 maternally expressed 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19264764 1621606 Meg3 maternally expressed 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:20610486 1621606 Meg3 maternally expressed 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17014736 1621606 Meg3 maternally expressed 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8903723 1621606 Meg3 maternally expressed 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19264764 1621606 Meg3 maternally expressed 3 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:19264764 1621606 Meg3 maternally expressed 3 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:17014736 1621606 Meg3 maternally expressed 3 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20610486 1621606 Meg3 maternally expressed 3 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:17014736 1621606 Meg3 maternally expressed 3 gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:20610486 1621606 Meg3 maternally expressed 3 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:16575184 1621606 Meg3 maternally expressed 3 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:17014736 1621606 Meg3 maternally expressed 3 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:20610486 1621606 Meg3 maternally expressed 3 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8903723 1621606 Meg3 maternally expressed 3 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:20610486 1621606 Meg3 maternally expressed 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19264764 1621606 Meg3 maternally expressed 3 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:20610486 1621606 Meg3 maternally expressed 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17014736 1621606 Meg3 maternally expressed 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19264764 1621606 Meg3 maternally expressed 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17014736 1621606 Meg3 maternally expressed 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20610486 1621606 Meg3 maternally expressed 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19264764 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000088 short mandible IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000111 cleft palate IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17336904 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18278031 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:9778514 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9162005 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16106363 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9162005 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:9778514 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9162005 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:20181743 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17336904 1621607 Mef2c myocyte enhancer factor 2C gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:22496871 1621607 Mef2c myocyte enhancer factor 2C gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22496871 1621607 Mef2c myocyte enhancer factor 2C gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17336904 1621607 Mef2c myocyte enhancer factor 2C gene MP:0001575 cyanosis IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10395786 1621607 Mef2c myocyte enhancer factor 2C gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:9162005 1621607 Mef2c myocyte enhancer factor 2C gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17336904 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002080 prenatal lethality IEA N RGD:5509061 20141003 MGI 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002081 perinatal lethality IEA N RGD:5509061 20141225 MGI 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22496871 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10395786 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:9162005 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16106363 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22496871 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002415 abnormal neutrophil differentiation IAGP N RGD:5509061 20141003 MGI PMID:18278031 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:18278031 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9778514 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:20181743 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:17336904 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:17336904 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20230406 MGI PMID:27898394 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:22496871 1621607 Mef2c myocyte enhancer factor 2C gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22496871 1621607 Mef2c myocyte enhancer factor 2C gene MP:0003228 abnormal sinus venosus morphology IAGP N RGD:5509061 20141003 MGI PMID:9162005 1621607 Mef2c myocyte enhancer factor 2C gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10395786 1621607 Mef2c myocyte enhancer factor 2C gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9778514 1621607 Mef2c myocyte enhancer factor 2C gene MP:0003542 abnormal vascular endothelial cell development IAGP N RGD:5509061 20141003 MGI PMID:9778514 1621607 Mef2c myocyte enhancer factor 2C gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:9778514 1621607 Mef2c myocyte enhancer factor 2C gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16106363 1621607 Mef2c myocyte enhancer factor 2C gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9162005 1621607 Mef2c myocyte enhancer factor 2C gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:9778514 1621607 Mef2c myocyte enhancer factor 2C gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:9162005 1621607 Mef2c myocyte enhancer factor 2C gene MP:0004424 temporal bone hypoplasia IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:17336904 1621607 Mef2c myocyte enhancer factor 2C gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:9778514 1621607 Mef2c myocyte enhancer factor 2C gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20181220 MGI PMID:21610032 1621607 Mef2c myocyte enhancer factor 2C gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9162005 1621607 Mef2c myocyte enhancer factor 2C gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9162005 1621607 Mef2c myocyte enhancer factor 2C gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20230406 MGI PMID:27898394 1621607 Mef2c myocyte enhancer factor 2C gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20200409 MGI PMID:30205047 1621607 Mef2c myocyte enhancer factor 2C gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17336904 1621607 Mef2c myocyte enhancer factor 2C gene MP:0008275 failure of endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17336904 1621607 Mef2c myocyte enhancer factor 2C gene MP:0008278 failure of sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:17336904 1621607 Mef2c myocyte enhancer factor 2C gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:20181743 1621607 Mef2c myocyte enhancer factor 2C gene MP:0009051 dilated distal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:20181743 1621607 Mef2c myocyte enhancer factor 2C gene MP:0009386 abnormal dermal melanocyte morphology IAGP N RGD:5509061 20181220 MGI PMID:21610032 1621607 Mef2c myocyte enhancer factor 2C gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20181220 MGI PMID:21610032 1621607 Mef2c myocyte enhancer factor 2C gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:17786239 1621607 Mef2c myocyte enhancer factor 2C gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17336904 1621607 Mef2c myocyte enhancer factor 2C gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17336904 1621607 Mef2c myocyte enhancer factor 2C gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9162005 1621607 Mef2c myocyte enhancer factor 2C gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20181743 1621607 Mef2c myocyte enhancer factor 2C gene MP:0011627 decreased skin pigmentation IAGP N RGD:5509061 20181220 MGI PMID:21610032 1621607 Mef2c myocyte enhancer factor 2C gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20181220 MGI PMID:21610032 1621607 Mef2c myocyte enhancer factor 2C gene MP:0030259 mandibular condyloid process hypoplasia IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0030285 mandibular coronoid process hypoplasia IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0030374 Meckel's cartilage hypoplasia IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0030377 zygomatic arch hypoplasia IAGP N RGD:5509061 20181108 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0030908 abnormal melanocyte differentiation IAGP N RGD:5509061 20181220 MGI PMID:21610032 1621607 Mef2c myocyte enhancer factor 2C gene MP:0031444 glossoptosis IAGP N RGD:5509061 20221027 MGI PMID:17420000 1621607 Mef2c myocyte enhancer factor 2C gene MP:0031545 increased sinoatrial node size IAGP N RGD:5509061 20240104 MGI PMID:16106363 1621608 Mef2a myocyte enhancer factor 2A gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:22496871 1621608 Mef2a myocyte enhancer factor 2A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22496871 1621608 Mef2a myocyte enhancer factor 2A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22496871 1621608 Mef2a myocyte enhancer factor 2A gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12379849 1621608 Mef2a myocyte enhancer factor 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12379849 1621608 Mef2a myocyte enhancer factor 2A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22496871 1621608 Mef2a myocyte enhancer factor 2A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22496871 1621608 Mef2a myocyte enhancer factor 2A gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22496871 1621608 Mef2a myocyte enhancer factor 2A gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:12379849 1621608 Mef2a myocyte enhancer factor 2A gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20230406 MGI PMID:27898394 1621608 Mef2a myocyte enhancer factor 2A gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:22496871 1621608 Mef2a myocyte enhancer factor 2A gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22496871 1621608 Mef2a myocyte enhancer factor 2A gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12379849 1621608 Mef2a myocyte enhancer factor 2A gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20230406 MGI PMID:27898394 1621608 Mef2a myocyte enhancer factor 2A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12379849 1621610 Mdm1 MDM1 nuclear protein gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:18805803 1621610 Mdm1 MDM1 nuclear protein gene MP:0002764 short tibia IEA N RGD:5509061 20231207 MGI 1621610 Mdm1 MDM1 nuclear protein gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18805803 1621610 Mdm1 MDM1 nuclear protein gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18805803 1621610 Mdm1 MDM1 nuclear protein gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18805803 1621610 Mdm1 MDM1 nuclear protein gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18805803 1621610 Mdm1 MDM1 nuclear protein gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18805803 1621610 Mdm1 MDM1 nuclear protein gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18805803 1621610 Mdm1 MDM1 nuclear protein gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 1621610 Mdm1 MDM1 nuclear protein gene MP:0005549 retina pigment epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18805803 1621610 Mdm1 MDM1 nuclear protein gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18805803 1621610 Mdm1 MDM1 nuclear protein gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:18805803 1621610 Mdm1 MDM1 nuclear protein gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:18805803 1621610 Mdm1 MDM1 nuclear protein gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:18805803 1621612 Mdfi MyoD family inhibitor gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0004677 truncated ribs IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621612 Mdfi MyoD family inhibitor gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9799236 1621615 Tpsab1 tryptase alpha/beta 1 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20200310 MGI PMID:19109198 1621615 Tpsab1 tryptase alpha/beta 1 gene MP:0005462 abnormal mast cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:19109198 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:18256672 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:17548588 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0002451 abnormal macrophage physiology IEA N RGD:5509061 20111116 MGI 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17548588 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17548588 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18256672 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18256672 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:17548588 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18256672 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:18256672 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0008563 decreased interferon-alpha secretion IEA N RGD:5509061 20111116 MGI 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0008565 decreased interferon-beta secretion IEA N RGD:5509061 20111116 MGI 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18256672 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21148800 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:21148800 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21148800 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0020913 increased susceptibility to Riboviria infection IEA N RGD:5509061 20200430 MGI 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0020916 increased susceptibility to Herpesvirales infection IEA N RGD:5509061 20200430 MGI 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0020931 increased susceptibility to Adenoviridae infection IEA N RGD:5509061 20200430 MGI 1621616 Ifnar2 interferon (alpha and beta) receptor 2 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IEA N RGD:5509061 20200430 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20210128 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20200310 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200402 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:11457893 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20200310 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20200310 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20200310 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200310 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20200310 MGI PMID:11457893 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20211118 MGI PMID:34078740 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20200310 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20200310 MGI PMID:11457893 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20200310 MGI PMID:11457893 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20200310 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20200310 MGI 1621624 Irgm1 immunity-related GTPase family M member 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20200402 MGI 1621625 Ier3 immediate early response 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19923449 1621625 Ier3 immediate early response 3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19923449 1621625 Ier3 immediate early response 3 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:19923449 1621625 Ier3 immediate early response 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:19923449 1621625 Ier3 immediate early response 3 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16166241 1621625 Ier3 immediate early response 3 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16166241 1621625 Ier3 immediate early response 3 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16166241 1621625 Ier3 immediate early response 3 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19923449 1621625 Ier3 immediate early response 3 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:19923449 1621625 Ier3 immediate early response 3 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22550081 1621625 Ier3 immediate early response 3 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:16166241 1621625 Ier3 immediate early response 3 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19923449 1621625 Ier3 immediate early response 3 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:19923449 1621625 Ier3 immediate early response 3 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:19923449 1621625 Ier3 immediate early response 3 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19923449 1621625 Ier3 immediate early response 3 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:19923449 1621625 Ier3 immediate early response 3 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:22550081 1621625 Ier3 immediate early response 3 gene MP:0008556 abnormal tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19923449 1621625 Ier3 immediate early response 3 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:19923449 1621625 Ier3 immediate early response 3 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19923449 1621625 Ier3 immediate early response 3 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22550081 1621625 Ier3 immediate early response 3 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:22550081 1621625 Ier3 immediate early response 3 gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:22550081 1621625 Ier3 immediate early response 3 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:16166241 1621626 Irf8 interferon regulatory factor 8 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20200310 MGI PMID:21045126 1621626 Irf8 interferon regulatory factor 8 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:21045126 1621626 Irf8 interferon regulatory factor 8 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20230413 MGI PMID:35732734 1621626 Irf8 interferon regulatory factor 8 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20200310 MGI PMID:15781580 1621626 Irf8 interferon regulatory factor 8 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20200310 MGI PMID:15781580 1621626 Irf8 interferon regulatory factor 8 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20200310 MGI PMID:22209163 1621626 Irf8 interferon regulatory factor 8 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:12832394 1621626 Irf8 interferon regulatory factor 8 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20200310 MGI PMID:12832394 1621626 Irf8 interferon regulatory factor 8 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:15781580 1621626 Irf8 interferon regulatory factor 8 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:12832394 1621626 Irf8 interferon regulatory factor 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:25024380 1621626 Irf8 interferon regulatory factor 8 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20200310 MGI PMID:21178004 1621626 Irf8 interferon regulatory factor 8 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20200310 MGI PMID:23297132 1621626 Irf8 interferon regulatory factor 8 gene MP:0002403 abnormal pre-B cell morphology IAGP N RGD:5509061 20200310 MGI PMID:12832394 1621626 Irf8 interferon regulatory factor 8 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20200310 MGI PMID:15781580 1621626 Irf8 interferon regulatory factor 8 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1621626 Irf8 interferon regulatory factor 8 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20210826 MGI 1621626 Irf8 interferon regulatory factor 8 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1621626 Irf8 interferon regulatory factor 8 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20200310 MGI PMID:12832394 1621626 Irf8 interferon regulatory factor 8 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210520 MGI 1621626 Irf8 interferon regulatory factor 8 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20200310 MGI PMID:21045126 1621626 Irf8 interferon regulatory factor 8 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20200618 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200310 MGI PMID:21178004 1621626 Irf8 interferon regulatory factor 8 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:12832394 1621626 Irf8 interferon regulatory factor 8 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:12832394 1621626 Irf8 interferon regulatory factor 8 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20200310 MGI PMID:15781580 1621626 Irf8 interferon regulatory factor 8 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 1621626 Irf8 interferon regulatory factor 8 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20201022 MGI 1621626 Irf8 interferon regulatory factor 8 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 1621626 Irf8 interferon regulatory factor 8 gene MP:0008071 absent B cells IAGP N RGD:5509061 20200310 MGI PMID:12832394 1621626 Irf8 interferon regulatory factor 8 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1621626 Irf8 interferon regulatory factor 8 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20200310 MGI 1621626 Irf8 interferon regulatory factor 8 gene MP:0008096 abnormal plasma cell number IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20200310 MGI PMID:15728463 1621626 Irf8 interferon regulatory factor 8 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20230413 MGI PMID:35732734 1621626 Irf8 interferon regulatory factor 8 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20200310 MGI PMID:15728463 1621626 Irf8 interferon regulatory factor 8 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20230413 MGI PMID:35732734 1621626 Irf8 interferon regulatory factor 8 gene MP:0008169 increased B-1b cell number IAGP N RGD:5509061 20200310 MGI PMID:21178004 1621626 Irf8 interferon regulatory factor 8 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20200310 MGI PMID:21178004 1621626 Irf8 interferon regulatory factor 8 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20200310 MGI PMID:21178004 1621626 Irf8 interferon regulatory factor 8 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20200310 MGI PMID:21178004 1621626 Irf8 interferon regulatory factor 8 gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20200310 MGI PMID:21178004 1621626 Irf8 interferon regulatory factor 8 gene MP:0008206 increased B-2 B cell number IAGP N RGD:5509061 20200310 MGI PMID:21178004 1621626 Irf8 interferon regulatory factor 8 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20200310 MGI PMID:21045126 1621626 Irf8 interferon regulatory factor 8 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:15781580 1621626 Irf8 interferon regulatory factor 8 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20200310 MGI PMID:15781580 1621626 Irf8 interferon regulatory factor 8 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1621626 Irf8 interferon regulatory factor 8 gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20230413 MGI PMID:35732734 1621626 Irf8 interferon regulatory factor 8 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:8861914 1621626 Irf8 interferon regulatory factor 8 gene MP:0031058 hepatosplenomegaly IAGP N RGD:5509061 20200618 MGI PMID:8861914 1621627 Gngt1 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:21632928 1621627 Gngt1 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 1 gene MP:0001999 photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:16102536 1621627 Gngt1 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18367617 1621627 Gngt1 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21632928 1621627 Gngt1 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18367617 1621627 Gngt1 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21632928 1621627 Gngt1 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:18367617 1621627 Gngt1 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 1 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18367617 1621627 Gngt1 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 1 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:21632928 1621627 Gngt1 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 1 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:18367617 1621628 Gnb4 guanine nucleotide binding protein (G protein), beta 4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1621628 Gnb4 guanine nucleotide binding protein (G protein), beta 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20181227 MGI 1621628 Gnb4 guanine nucleotide binding protein (G protein), beta 4 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210826 MGI 1621628 Gnb4 guanine nucleotide binding protein (G protein), beta 4 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210128 MGI 1621628 Gnb4 guanine nucleotide binding protein (G protein), beta 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1621628 Gnb4 guanine nucleotide binding protein (G protein), beta 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1621628 Gnb4 guanine nucleotide binding protein (G protein), beta 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0000064 failure of bone resorption IAGP N RGD:5509061 20141003 MGI PMID:1155801 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:12627228 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0000445 short snout IEA N RGD:5509061 20111116 MGI 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0001290 delayed eyelid opening IEA N RGD:5509061 20111116 MGI 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0001851 eye inflammation IEA N RGD:5509061 20111116 MGI 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:1155801 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0003932 abnormal molar crown morphology IEA N RGD:5509061 20111116 MGI 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0004830 short incisors IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0005150 cachexia IEA N RGD:5509061 20111116 MGI 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0008274 failure of bone ossification IEA N RGD:5509061 20111116 MGI 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0008733 abnormal hair shaft melanin granule distribution IAGP N RGD:5509061 20190103 MGI PMID:24820037 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0030089 short lower incisors IAGP N RGD:5509061 20170928 MGI PMID:1155801 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0030236 abnormal mental foramen morphology IEA N RGD:5509061 20171019 MGI 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0030302 abnormal maxillary zygomatic process morphology IAGP N RGD:5509061 20171102 MGI PMID:23160729 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0030451 abnormal dentin mineralization IEA N RGD:5509061 20180215 MGI 1621630 Ostm1 osteopetrosis associated transmembrane protein 1 gene MP:0030494 abnormal molar root morphology IEA N RGD:5509061 20180125 MGI 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10903175 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:10903175 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:10903175 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:20930146 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20170105 MGI 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0000296 absent trabeculae carneae IAGP N RGD:5509061 20141003 MGI PMID:10903175 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:20930146 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:10903175 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14681043 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10903175 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20930146 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10903175 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:14681043 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:14681043 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:20930146 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:14681043 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:14681043 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20930146 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:10903175 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:20930146 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10903175 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20930146 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:15659592 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:20930146 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:20930146 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15659592 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10903175 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:20930146 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:22982984 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:22982984 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:20930146 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0010559 heart block IAGP N RGD:5509061 20141003 MGI PMID:10903175 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10903175 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14681043 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20930146 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22982984 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0011953 prolonged PQ interval IAGP N RGD:5509061 20141003 MGI PMID:22982984 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14681043 1621631 Gjc1 gap junction protein, gamma 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1621633 Ackr1 atypical chemokine receptor 1 (Duffy blood group) gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:17416748 1621633 Ackr1 atypical chemokine receptor 1 (Duffy blood group) gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12646177 1621633 Ackr1 atypical chemokine receptor 1 (Duffy blood group) gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:10961863 1621633 Ackr1 atypical chemokine receptor 1 (Duffy blood group) gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:12646177 1621633 Ackr1 atypical chemokine receptor 1 (Duffy blood group) gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:20643340 1621633 Ackr1 atypical chemokine receptor 1 (Duffy blood group) gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20220922 MGI PMID:17416748 1621633 Ackr1 atypical chemokine receptor 1 (Duffy blood group) gene MP:0013615 increased volumetric bone mineral density IAGP N RGD:5509061 20220922 MGI PMID:17416748 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21333348 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:21333348 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19103808 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:8684484 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21333348 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:21333348 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:8684484 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:8684484 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:8684484 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0004149 increased bone strength IAGP N RGD:5509061 20141003 MGI PMID:8684484 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:8684484 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21333348 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:21333348 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:21333348 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:8684484 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:21333348 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:21333348 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:8684484 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21333348 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:21333348 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:8684484 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21333348 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20170803 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:17693256 1621634 Bglap bone gamma carboxyglutamate protein gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:17693256 1621637 Bcl2a1d B cell leukemia/lymphoma 2 related protein A1d gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20190117 MGI PMID:28085150 1621637 Bcl2a1d B cell leukemia/lymphoma 2 related protein A1d gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 1621637 Bcl2a1d B cell leukemia/lymphoma 2 related protein A1d gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 1621637 Bcl2a1d B cell leukemia/lymphoma 2 related protein A1d gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 1621637 Bcl2a1d B cell leukemia/lymphoma 2 related protein A1d gene MP:0010836 decreased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 1621637 Bcl2a1d B cell leukemia/lymphoma 2 related protein A1d gene MP:0010842 decreased central memory CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 1621637 Bcl2a1d B cell leukemia/lymphoma 2 related protein A1d gene MP:0010845 decreased effector memory CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 1621639 Bcl2a1b B cell leukemia/lymphoma 2 related protein A1b gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20190117 MGI PMID:28085150 1621639 Bcl2a1b B cell leukemia/lymphoma 2 related protein A1b gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 1621639 Bcl2a1b B cell leukemia/lymphoma 2 related protein A1b gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 1621639 Bcl2a1b B cell leukemia/lymphoma 2 related protein A1b gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 1621639 Bcl2a1b B cell leukemia/lymphoma 2 related protein A1b gene MP:0010836 decreased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 1621639 Bcl2a1b B cell leukemia/lymphoma 2 related protein A1b gene MP:0010842 decreased central memory CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 1621639 Bcl2a1b B cell leukemia/lymphoma 2 related protein A1b gene MP:0010845 decreased effector memory CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 1621640 Barx2 BarH-like homeobox 2 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20201231 MGI 1621640 Barx2 BarH-like homeobox 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:15728386 1621640 Barx2 BarH-like homeobox 2 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:15728386 1621640 Barx2 BarH-like homeobox 2 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:15728386 1621640 Barx2 BarH-like homeobox 2 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141003 MGI PMID:15728386 1621640 Barx2 BarH-like homeobox 2 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20160421 MGI 1621640 Barx2 BarH-like homeobox 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15728386 1621640 Barx2 BarH-like homeobox 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:15728386 1621640 Barx2 BarH-like homeobox 2 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160421 MGI 1621640 Barx2 BarH-like homeobox 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200402 MGI 1621640 Barx2 BarH-like homeobox 2 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15728386 1621640 Barx2 BarH-like homeobox 2 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20160421 MGI 1621640 Barx2 BarH-like homeobox 2 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1621640 Barx2 BarH-like homeobox 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1621640 Barx2 BarH-like homeobox 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1621640 Barx2 BarH-like homeobox 2 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0009420 skeletal muscle endomysial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 1621640 Barx2 BarH-like homeobox 2 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22076929 1621640 Barx2 BarH-like homeobox 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1621640 Barx2 BarH-like homeobox 2 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:22076929 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:14973294 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:14973294 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:14973294 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000071 axial skeleton hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000080 abnormal exoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:12204261 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:12204261 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12204261 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:12204261 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:23645682 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:15829524 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15829524 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15829524 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:12204261 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000588 thick tail IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15829524 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23645682 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0001268 barrel chest IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15329346 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12204261 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21913311 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:15829524 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12204261 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:15829524 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0003283 abnormal digestive organ placement IAGP N RGD:5509061 20141003 MGI PMID:15329346 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23645682 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:15329346 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15829524 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004443 absent supraoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004445 small exoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004447 small basioccipital bone IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004461 basisphenoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:12204261 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004626 vertebral compression IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004652 small caudal vertebrae IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004659 abnormal odontoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004667 vertebral body hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004668 absent vertebral body IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004683 absent intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:19208343 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004711 persistence of notochord tissue IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0004733 abnormal thoracic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:14973294 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:12204261 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0005226 abnormal vertebral arch development IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0005227 abnormal vertebral body development IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:19208343 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:12204261 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0008381 absent gonial bone IAGP N RGD:5509061 20141003 MGI PMID:14973294 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0008382 gonial bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14973294 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0008385 absent basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:19208343 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0008802 abnormal intestinal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23645682 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23645682 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0009609 absent basioccipital bone IAGP N RGD:5509061 20171026 MGI PMID:19208343 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0009917 abnormal hyoid bone body morphology IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:23645682 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20141003 MGI PMID:23645682 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0010729 absent arcus anterior IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0010731 absent ventral tubercle of atlas IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0010780 abnormal stomach smooth muscle circular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15829524 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0010785 abnormal stomach pyloric region morphology IAGP N RGD:5509061 20141003 MGI PMID:15829524 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0010802 abnormal intestinal enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23645682 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10572046 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11523821 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12204261 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23645682 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12204261 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0013575 abnormal forestomach-glandular stomach junction morphology IAGP N RGD:5509061 20150305 MGI PMID:15829524 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0013576 small forestomach IAGP N RGD:5509061 20150305 MGI PMID:15829524 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0030027 basioccipital bone hypoplasia IAGP N RGD:5509061 20170810 MGI PMID:10449756 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0030027 basioccipital bone hypoplasia IAGP N RGD:5509061 20171026 MGI PMID:10886375 1621641 Nkx3-2 NK3 homeobox 2 gene MP:0030084 tympanic ring hypoplasia IAGP N RGD:5509061 20241031 MGI PMID:14973294 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20141003 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20141003 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0000322 increased granulocyte number IEA N RGD:5509061 20211021 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15152264 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0001513 limb grasping IEA N RGD:5509061 20181227 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15152264 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15152264 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15152264 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15152264 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15152264 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20181227 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:15152264 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:15152264 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0004974 decreased regulatory T cell number IEA N RGD:5509061 20201022 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20190404 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20141003 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15152264 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0005387 immune system phenotype IEA N RGD:5509061 20210826 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0005425 increased macrophage cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20211021 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20181227 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0005573 increased pulmonary respiratory rate IEA N RGD:5509061 20210128 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008039 increased NK T cell number IEA N RGD:5509061 20211021 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20210826 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190404 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008168 decreased B-1a cell number IEA N RGD:5509061 20211021 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008174 decreased follicular B cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008179 absent germinal center B cells IAGP N RGD:5509061 20141003 MGI PMID:15152264 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008182 decreased marginal zone B cell number IEA N RGD:5509061 20111116 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008190 decreased transitional stage B cell number IEA N RGD:5509061 20211021 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20210826 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15152264 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008214 increased immature B cell number IEA N RGD:5509061 20141003 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20220811 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15152264 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:15152264 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:15152264 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:15152264 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20211021 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20181227 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20181227 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0010373 myeloid hyperplasia IEA N RGD:5509061 20111116 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20181227 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IEA N RGD:5509061 20201022 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20201022 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0010851 decreased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0011896 increased circulating unsaturated transferrin level IEA N RGD:5509061 20181227 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0011940 decreased food intake IEA N RGD:5509061 20181227 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0012767 increased KLRG1-positive NK cell number IEA N RGD:5509061 20141003 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013022 increased Ly6C high monocyte number IEA N RGD:5509061 20181227 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013025 increased Ly6C low monocyte number IEA N RGD:5509061 20141003 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013154 increased KLRG1+ CD8 alpha-beta T cell number IEA N RGD:5509061 20160811 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013157 increased KLRG1+ CD4 alpha-beta T cell number IEA N RGD:5509061 20141003 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013424 increased KLRG1-positive gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013426 decreased memory-marker NK cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013427 increased memory-marker NK cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013430 increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013433 increased KLRG1-positive CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013510 decreased CD4-negative NK T cell number IEA N RGD:5509061 20210826 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013513 decreased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20210826 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013514 increased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013517 increased KLRG1-positive CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013649 decreased CD11b-high dendritic cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013651 increased CD11b-low dendritic cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013654 increased CD103-positive CD11b-low dendritic cell number IEA N RGD:5509061 20201231 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013669 decreased Ly6C-positive immature NK cell number IEA N RGD:5509061 20211021 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013675 decreased Ly6C-positive mature NK cell number IEA N RGD:5509061 20211021 MGI 1621642 Bach2 BTB and CNC homology, basic leucine zipper transcription factor 2 gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20201231 MGI 1621802 Klk13 kallikrein related-peptidase 13 gene MP:0001297 microphthalmia IEA N RGD:5509061 20201022 MGI 1621802 Klk13 kallikrein related-peptidase 13 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1621802 Klk13 kallikrein related-peptidase 13 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20201022 MGI 1621802 Klk13 kallikrein related-peptidase 13 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1621826 Clrn2 clarin 2 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20201015 MGI PMID:27534441 1621826 Clrn2 clarin 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20201022 MGI 1621826 Clrn2 clarin 2 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1621826 Clrn2 clarin 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20190502 MGI 1621826 Clrn2 clarin 2 gene MP:0001967 deafness IAGP N RGD:5509061 20201015 MGI PMID:27534441 1621826 Clrn2 clarin 2 gene MP:0001967 deafness IAGP N RGD:5509061 20201015 MGI PMID:31448880 1621826 Clrn2 clarin 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230601 MGI 1621826 Clrn2 clarin 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20190502 MGI 1621826 Clrn2 clarin 2 gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20201015 MGI PMID:31448880 1621826 Clrn2 clarin 2 gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20201015 MGI PMID:31448880 1621826 Clrn2 clarin 2 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20201015 MGI PMID:31448880 1621826 Clrn2 clarin 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1621826 Clrn2 clarin 2 gene MP:0004749 nonsyndromic hearing loss IAGP N RGD:5509061 20201015 MGI PMID:31448880 1621826 Clrn2 clarin 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1621826 Clrn2 clarin 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20190502 MGI 1621826 Clrn2 clarin 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20190502 MGI 1621826 Clrn2 clarin 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20201015 MGI PMID:31448880 1621827 Angptl8 angiopoietin-like 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150305 MGI PMID:24043787 1621827 Angptl8 angiopoietin-like 8 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20562862 1621827 Angptl8 angiopoietin-like 8 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22569073 1621827 Angptl8 angiopoietin-like 8 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20150305 MGI PMID:24043787 1621827 Angptl8 angiopoietin-like 8 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20150305 MGI PMID:24043787 1621827 Angptl8 angiopoietin-like 8 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20150305 MGI PMID:24043787 1621827 Angptl8 angiopoietin-like 8 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20150305 MGI PMID:24043787 1621827 Angptl8 angiopoietin-like 8 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20150305 MGI PMID:24043787 1621827 Angptl8 angiopoietin-like 8 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20150305 MGI PMID:24043787 1621827 Angptl8 angiopoietin-like 8 gene MP:0011578 increased lipoprotein lipase activity IAGP N RGD:5509061 20150305 MGI PMID:24043787 1621827 Angptl8 angiopoietin-like 8 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20150305 MGI PMID:24043787 1621850 Alkal1 ALK and LTK ligand 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240704 MGI PMID:35412887 1621850 Alkal1 ALK and LTK ligand 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20240704 MGI PMID:35412887 1621864 Iqgap2 IQ motif containing GTPase activating protein 2 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:18180285 1621864 Iqgap2 IQ motif containing GTPase activating protein 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 1621864 Iqgap2 IQ motif containing GTPase activating protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18180285 1621864 Iqgap2 IQ motif containing GTPase activating protein 2 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:18180285 1621864 Iqgap2 IQ motif containing GTPase activating protein 2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18180285 1621864 Iqgap2 IQ motif containing GTPase activating protein 2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23951254 1621864 Iqgap2 IQ motif containing GTPase activating protein 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:18180285 1621864 Iqgap2 IQ motif containing GTPase activating protein 2 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18180285 1621864 Iqgap2 IQ motif containing GTPase activating protein 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1621864 Iqgap2 IQ motif containing GTPase activating protein 2 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18180285 1621864 Iqgap2 IQ motif containing GTPase activating protein 2 gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:18180285 1621872 Sp140 Sp140 nuclear body protein gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20221201 MGI PMID:34151776 1621872 Sp140 Sp140 nuclear body protein gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20221201 MGI PMID:34151776 1621876 Fbxw20 F-box and WD-40 domain protein 20 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210128 MGI 1621876 Fbxw20 F-box and WD-40 domain protein 20 gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20210128 MGI 1621876 Fbxw20 F-box and WD-40 domain protein 20 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1621876 Fbxw20 F-box and WD-40 domain protein 20 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1621876 Fbxw20 F-box and WD-40 domain protein 20 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1621876 Fbxw20 F-box and WD-40 domain protein 20 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1621876 Fbxw20 F-box and WD-40 domain protein 20 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1621876 Fbxw20 F-box and WD-40 domain protein 20 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1621876 Fbxw20 F-box and WD-40 domain protein 20 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20210128 MGI 1621876 Fbxw20 F-box and WD-40 domain protein 20 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1621876 Fbxw20 F-box and WD-40 domain protein 20 gene MP:0003883 enlarged stomach IEA N RGD:5509061 20210128 MGI 1621877 BC048562 cDNA sequence BC048562 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210128 MGI 1621877 BC048562 cDNA sequence BC048562 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1621877 BC048562 cDNA sequence BC048562 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IEA N RGD:5509061 20220519 MGI 1621877 BC048562 cDNA sequence BC048562 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1621877 BC048562 cDNA sequence BC048562 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 1621878 Iho1 interactor of HORMAD1 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20230420 MGI PMID:31000436 1621879 Amt aminomethyltransferase gene MP:0000111 cleft palate IEA N RGD:5509061 20231207 MGI 1621879 Amt aminomethyltransferase gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22171071 1621879 Amt aminomethyltransferase gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:22171071 1621879 Amt aminomethyltransferase gene MP:0001293 anophthalmia IEA N RGD:5509061 20231207 MGI 1621879 Amt aminomethyltransferase gene MP:0001297 microphthalmia IEA N RGD:5509061 20231207 MGI 1621879 Amt aminomethyltransferase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20231207 MGI 1621879 Amt aminomethyltransferase gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22171071 1621879 Amt aminomethyltransferase gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22171071 1621879 Amt aminomethyltransferase gene MP:0002764 short tibia IEA N RGD:5509061 20231207 MGI 1621879 Amt aminomethyltransferase gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20231207 MGI 1621879 Amt aminomethyltransferase gene MP:0003054 spina bifida IEA N RGD:5509061 20231207 MGI 1621879 Amt aminomethyltransferase gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20231207 MGI 1621879 Amt aminomethyltransferase gene MP:0003257 abnormal abdominal wall morphology IEA N RGD:5509061 20231207 MGI 1621879 Amt aminomethyltransferase gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20231207 MGI 1621879 Amt aminomethyltransferase gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20231207 MGI 1621879 Amt aminomethyltransferase gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:22171071 1621879 Amt aminomethyltransferase gene MP:0008797 facial cleft IEA N RGD:5509061 20231207 MGI 1621879 Amt aminomethyltransferase gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 1621879 Amt aminomethyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1621879 Amt aminomethyltransferase gene MP:0011495 abnormal head shape IEA N RGD:5509061 20231207 MGI 1621879 Amt aminomethyltransferase gene MP:0011496 abnormal head size IEA N RGD:5509061 20231207 MGI 1621886 Gm5617 predicted gene 5617 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1621891 Spink6 serine peptidase inhibitor, Kazal type 6 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 1621891 Spink6 serine peptidase inhibitor, Kazal type 6 gene MP:0003884 decreased macrophage cell number IEA N RGD:5509061 20210826 MGI 1621891 Spink6 serine peptidase inhibitor, Kazal type 6 gene MP:0013669 decreased Ly6C-positive immature NK cell number IEA N RGD:5509061 20211021 MGI 1621891 Spink6 serine peptidase inhibitor, Kazal type 6 gene MP:0013676 increased Ly6C-positive mature NK cell number IEA N RGD:5509061 20211021 MGI 1621892 Spink14 serine peptidase inhibitor, Kazal type 14 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20201022 MGI 1621892 Spink14 serine peptidase inhibitor, Kazal type 14 gene MP:0003884 decreased macrophage cell number IEA N RGD:5509061 20201231 MGI 1621892 Spink14 serine peptidase inhibitor, Kazal type 14 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1621892 Spink14 serine peptidase inhibitor, Kazal type 14 gene MP:0004794 increased anti-nuclear antigen antibody level IEA N RGD:5509061 20201022 MGI 1621892 Spink14 serine peptidase inhibitor, Kazal type 14 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20201231 MGI 1621892 Spink14 serine peptidase inhibitor, Kazal type 14 gene MP:0013427 increased memory-marker NK cell number IEA N RGD:5509061 20201231 MGI 1621892 Spink14 serine peptidase inhibitor, Kazal type 14 gene MP:0013666 decreased immature NK cell number IEA N RGD:5509061 20201231 MGI 1621892 Spink14 serine peptidase inhibitor, Kazal type 14 gene MP:0013672 decreased mature NK cell number IEA N RGD:5509061 20201231 MGI 1621935 Tldc2 TBC/LysM associated domain containing 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1621935 Tldc2 TBC/LysM associated domain containing 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 1621944 Poc1b POC1 centriolar protein B gene MP:0001925 male infertility IAGP N RGD:5509061 20231005 MGI PMID:37070736 1621944 Poc1b POC1 centriolar protein B gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20200514 MGI 1621944 Poc1b POC1 centriolar protein B gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20231005 MGI PMID:37070736 1621944 Poc1b POC1 centriolar protein B gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20231005 MGI PMID:37070736 1621944 Poc1b POC1 centriolar protein B gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20231005 MGI PMID:37070736 1621944 Poc1b POC1 centriolar protein B gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20231005 MGI PMID:37070736 1621944 Poc1b POC1 centriolar protein B gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20231005 MGI PMID:37070736 1621944 Poc1b POC1 centriolar protein B gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20231005 MGI PMID:37070736 1621944 Poc1b POC1 centriolar protein B gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20231005 MGI PMID:37070736 1621944 Poc1b POC1 centriolar protein B gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20231005 MGI PMID:37070736 1621944 Poc1b POC1 centriolar protein B gene MP:0009837 abnormal sperm end piece morphology IAGP N RGD:5509061 20231005 MGI PMID:37070736 1621944 Poc1b POC1 centriolar protein B gene MP:0020869 immotile sperm IAGP N RGD:5509061 20231005 MGI PMID:37070736 1621944 Poc1b POC1 centriolar protein B gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20231005 MGI PMID:37070736 1621944 Poc1b POC1 centriolar protein B gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20231005 MGI PMID:37070736 1621945 Top6bl TOP6B like initiator of meiotic double strand breaks gene MP:0001147 small testis IAGP N RGD:5509061 20161020 MGI PMID:26917764 1621945 Top6bl TOP6B like initiator of meiotic double strand breaks gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20161020 MGI PMID:26917764 1621945 Top6bl TOP6B like initiator of meiotic double strand breaks gene MP:0005159 azoospermia IAGP N RGD:5509061 20161020 MGI PMID:26917764 1621945 Top6bl TOP6B like initiator of meiotic double strand breaks gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20161020 MGI PMID:26917764 1621945 Top6bl TOP6B like initiator of meiotic double strand breaks gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20161020 MGI PMID:26917764 1621945 Top6bl TOP6B like initiator of meiotic double strand breaks gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20161020 MGI PMID:26917764 1621945 Top6bl TOP6B like initiator of meiotic double strand breaks gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20161020 MGI PMID:26917764 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0000520 absent kidney IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0000914 exencephaly IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0001147 small testis IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20190502 MGI 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20190502 MGI 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0006425 absent Mullerian ducts IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0009073 absent Wolffian ducts IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0010788 stomach hypoplasia IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0011493 double ureter IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621948 Greb1l growth regulation by estrogen in breast cancer-like gene MP:0011760 abnormal ureteric bud tip morphology IAGP N RGD:5509061 20180712 MGI PMID:29100091 1621949 Prob1 proline rich basic protein 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220519 MGI 1621952 Garem1 GRB2 associated regulator of MAPK1 subtype 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1621952 Garem1 GRB2 associated regulator of MAPK1 subtype 1 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1621952 Garem1 GRB2 associated regulator of MAPK1 subtype 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1621952 Garem1 GRB2 associated regulator of MAPK1 subtype 1 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1621952 Garem1 GRB2 associated regulator of MAPK1 subtype 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 1621952 Garem1 GRB2 associated regulator of MAPK1 subtype 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230202 MGI PMID:36084556 1621952 Garem1 GRB2 associated regulator of MAPK1 subtype 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1621952 Garem1 GRB2 associated regulator of MAPK1 subtype 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1621952 Garem1 GRB2 associated regulator of MAPK1 subtype 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1621954 Cdkl4 cyclin dependent kinase like 4 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1621954 Cdkl4 cyclin dependent kinase like 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1621955 Arhgef33 Rho guanine nucleotide exchange factor 33 gene MP:0000745 tremors IEA N RGD:5509061 20230119 MGI 1621955 Arhgef33 Rho guanine nucleotide exchange factor 33 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230119 MGI 1621955 Arhgef33 Rho guanine nucleotide exchange factor 33 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20231207 MGI 1621955 Arhgef33 Rho guanine nucleotide exchange factor 33 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230119 MGI 1621957 Tmem232 transmembrane protein 232 gene MP:0001925 male infertility IAGP N RGD:5509061 20230810 MGI PMID:37371084 1621957 Tmem232 transmembrane protein 232 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230810 MGI PMID:37371084 1621957 Tmem232 transmembrane protein 232 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230810 MGI PMID:37371084 1621957 Tmem232 transmembrane protein 232 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20230810 MGI PMID:37371084 1621957 Tmem232 transmembrane protein 232 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20230810 MGI PMID:37371084 1621957 Tmem232 transmembrane protein 232 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20230810 MGI PMID:37371084 1621957 Tmem232 transmembrane protein 232 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20230810 MGI PMID:37371084 1621957 Tmem232 transmembrane protein 232 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20230810 MGI PMID:37371084 1621957 Tmem232 transmembrane protein 232 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20230810 MGI PMID:37371084 1621959 Ksr2 kinase suppressor of ras 2 gene MP:0001260 increased body weight IEA N RGD:5509061 20151015 MGI 1621959 Ksr2 kinase suppressor of ras 2 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:21127480 1621959 Ksr2 kinase suppressor of ras 2 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18719666 1621959 Ksr2 kinase suppressor of ras 2 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:21127480 1621963 Nlrp9c NLR family, pyrin domain containing 9C gene MP:0001935 decreased litter size IAGP N RGD:5509061 20210415 MGI PMID:32413845 1621963 Nlrp9c NLR family, pyrin domain containing 9C gene MP:0002293 long gestation period IAGP N RGD:5509061 20210415 MGI PMID:32413845 1621963 Nlrp9c NLR family, pyrin domain containing 9C gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20210415 MGI PMID:32413845 1621963 Nlrp9c NLR family, pyrin domain containing 9C gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20210415 MGI PMID:32413845 1621963 Nlrp9c NLR family, pyrin domain containing 9C gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20210415 MGI PMID:32413845 1621963 Nlrp9c NLR family, pyrin domain containing 9C gene MP:0012128 abnormal blastocyst formation IAGP N RGD:5509061 20210415 MGI PMID:32413845 1621963 Nlrp9c NLR family, pyrin domain containing 9C gene MP:0012129 failure of blastocyst formation IAGP N RGD:5509061 20210415 MGI PMID:32413845 1621964 Tmem145 transmembrane protein 145 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1621964 Tmem145 transmembrane protein 145 gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1621964 Tmem145 transmembrane protein 145 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1621964 Tmem145 transmembrane protein 145 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210128 MGI 1621964 Tmem145 transmembrane protein 145 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1621964 Tmem145 transmembrane protein 145 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1621964 Tmem145 transmembrane protein 145 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1621964 Tmem145 transmembrane protein 145 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1621964 Tmem145 transmembrane protein 145 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1621964 Tmem145 transmembrane protein 145 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1621964 Tmem145 transmembrane protein 145 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 1621964 Tmem145 transmembrane protein 145 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20160929 MGI PMID:27534441 1621964 Tmem145 transmembrane protein 145 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20201022 MGI 1621965 Ceacam16 CEA cell adhesion molecule 16 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20160421 MGI 1621965 Ceacam16 CEA cell adhesion molecule 16 gene MP:0004749 nonsyndromic hearing loss IAGP N RGD:5509061 20141003 MGI PMID:22544735 1621965 Ceacam16 CEA cell adhesion molecule 16 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160421 MGI 1621965 Ceacam16 CEA cell adhesion molecule 16 gene MP:0006336 abnormal otoacoustic response IAGP N RGD:5509061 20160421 MGI PMID:25080593 1621965 Ceacam16 CEA cell adhesion molecule 16 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:22544735 1621965 Ceacam16 CEA cell adhesion molecule 16 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20160421 MGI PMID:25080593 1621965 Ceacam16 CEA cell adhesion molecule 16 gene MP:0012121 sclerocornea IEA N RGD:5509061 20160421 MGI 1621965 Ceacam16 CEA cell adhesion molecule 16 gene MP:0013962 absent Hensen stripe IAGP N RGD:5509061 20160421 MGI PMID:25080593 1621965 Ceacam16 CEA cell adhesion molecule 16 gene MP:0014091 abnormal tectorial membrane striated-sheet matrix morphology IAGP N RGD:5509061 20160421 MGI PMID:25080593 1621965 Ceacam16 CEA cell adhesion molecule 16 gene MP:0014407 decreased distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:22544735 1621965 Ceacam16 CEA cell adhesion molecule 16 gene MP:0014409 decreased distortion product otoacoustic emission amplitude IAGP N RGD:5509061 20240405 MGI PMID:22544735 1621971 B4galnt3 beta-1,4-N-acetyl-galactosaminyl transferase 3 gene MP:0001391 abnormal tail movements IEA N RGD:5509061 20141003 MGI 1621971 B4galnt3 beta-1,4-N-acetyl-galactosaminyl transferase 3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20160804 MGI 1621973 Unc80 unc-80, NALCN activator gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20201022 MGI 1621973 Unc80 unc-80, NALCN activator gene MP:0001258 decreased body length IEA N RGD:5509061 20201022 MGI 1621973 Unc80 unc-80, NALCN activator gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1621973 Unc80 unc-80, NALCN activator gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1621973 Unc80 unc-80, NALCN activator gene MP:0001957 apnea IAGP N RGD:5509061 20200903 MGI PMID:32620897 1621973 Unc80 unc-80, NALCN activator gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20200903 MGI PMID:32620897 1621973 Unc80 unc-80, NALCN activator gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20211021 MGI 1621973 Unc80 unc-80, NALCN activator gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20200903 MGI PMID:32620897 1621973 Unc80 unc-80, NALCN activator gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20211021 MGI 1621973 Unc80 unc-80, NALCN activator gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200903 MGI PMID:32620897 1621973 Unc80 unc-80, NALCN activator gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200514 MGI 1621976 Ankrd44 ankyrin repeat domain 44 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 1621976 Ankrd44 ankyrin repeat domain 44 gene MP:0011496 abnormal head size IEA N RGD:5509061 20231207 MGI 1621980 Ppfia2 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20200310 MGI 1621980 Ppfia2 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 2 gene MP:0001410 head bobbing IEA N RGD:5509061 20200310 MGI 1621980 Ppfia2 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20210128 MGI 1621980 Ppfia2 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 2 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20210128 MGI 1621980 Ppfia2 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20210128 MGI 1621986 Ptgs2os prostaglandin-endoperoxide synthase 2, opposite strand gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20220804 MGI PMID:35365562 1621986 Ptgs2os prostaglandin-endoperoxide synthase 2, opposite strand gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20220804 MGI PMID:35365562 1621986 Ptgs2os prostaglandin-endoperoxide synthase 2, opposite strand gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20220804 MGI PMID:35365562 1621986 Ptgs2os prostaglandin-endoperoxide synthase 2, opposite strand gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20220804 MGI PMID:35365562 1621986 Ptgs2os prostaglandin-endoperoxide synthase 2, opposite strand gene MP:0031247 decreased CCL3 level IAGP N RGD:5509061 20220804 MGI PMID:35365562 1621986 Ptgs2os prostaglandin-endoperoxide synthase 2, opposite strand gene MP:0031250 decreased circulating CCL3 level IAGP N RGD:5509061 20220804 MGI PMID:35365562 1621987 Sidt1 SID1 transmembrane family, member 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1621987 Sidt1 SID1 transmembrane family, member 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20170105 MGI 1621989 Nup62cl nucleoporin 62 C-terminal like gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20240523 MGI 1621989 Nup62cl nucleoporin 62 C-terminal like gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20240523 MGI 1621989 Nup62cl nucleoporin 62 C-terminal like gene MP:0001314 cornea opacity IEA N RGD:5509061 20240523 MGI 1621989 Nup62cl nucleoporin 62 C-terminal like gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1621989 Nup62cl nucleoporin 62 C-terminal like gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1621990 Nynrin NYN domain and retroviral integrase containing gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20200514 MGI 1621994 Ift56 intraflagellar transport 56 gene MP:0000111 cleft palate IEA N RGD:5509061 20240523 MGI 1621994 Ift56 intraflagellar transport 56 gene MP:0000161 scoliosis IEA N RGD:5509061 20150910 MGI 1621994 Ift56 intraflagellar transport 56 gene MP:0000562 polydactyly IEA N RGD:5509061 20151022 MGI 1621994 Ift56 intraflagellar transport 56 gene MP:0001147 small testis IAGP N RGD:5509061 20150910 MGI PMID:5088020 1621994 Ift56 intraflagellar transport 56 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151015 MGI PMID:25340710 1621994 Ift56 intraflagellar transport 56 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20240523 MGI 1621994 Ift56 intraflagellar transport 56 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20150910 MGI PMID:142347 1621994 Ift56 intraflagellar transport 56 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20150910 MGI PMID:5088020 1621994 Ift56 intraflagellar transport 56 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20150910 MGI PMID:5088020 1621994 Ift56 intraflagellar transport 56 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20150910 MGI PMID:5088020 1621994 Ift56 intraflagellar transport 56 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20150910 MGI PMID:142347 1621994 Ift56 intraflagellar transport 56 gene MP:0001925 male infertility IAGP N RGD:5509061 20150910 MGI PMID:5088020 1621994 Ift56 intraflagellar transport 56 gene MP:0001925 male infertility IAGP N RGD:5509061 20150910 MGI PMID:7317942 1621994 Ift56 intraflagellar transport 56 gene MP:0001925 male infertility IAGP N RGD:5509061 20150910 MGI PMID:872193 1621994 Ift56 intraflagellar transport 56 gene MP:0001925 male infertility IAGP N RGD:5509061 20150910 MGI PMID:9674995 1621994 Ift56 intraflagellar transport 56 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20150910 MGI PMID:5088020 1621994 Ift56 intraflagellar transport 56 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20150910 MGI PMID:7317942 1621994 Ift56 intraflagellar transport 56 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20150910 MGI PMID:872193 1621994 Ift56 intraflagellar transport 56 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20150910 MGI PMID:9674995 1621994 Ift56 intraflagellar transport 56 gene MP:0002083 premature death IAGP N RGD:5509061 20150910 MGI PMID:7317942 1621994 Ift56 intraflagellar transport 56 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20151015 MGI PMID:25340710 1621994 Ift56 intraflagellar transport 56 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20151015 MGI PMID:25340710 1621994 Ift56 intraflagellar transport 56 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20150910 MGI PMID:872193 1621994 Ift56 intraflagellar transport 56 gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20151015 MGI PMID:25340710 1621994 Ift56 intraflagellar transport 56 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20240523 MGI 1621994 Ift56 intraflagellar transport 56 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20151015 MGI PMID:25340710 1621994 Ift56 intraflagellar transport 56 gene MP:0004131 abnormal motile primary cilium morphology IAGP N RGD:5509061 20151015 MGI PMID:25340710 1621994 Ift56 intraflagellar transport 56 gene MP:0004289 abnormal bony labyrinth IAGP N RGD:5509061 20151015 MGI PMID:25340710 1621994 Ift56 intraflagellar transport 56 gene MP:0005159 azoospermia IAGP N RGD:5509061 20150910 MGI PMID:5088020 1621994 Ift56 intraflagellar transport 56 gene MP:0005159 azoospermia IAGP N RGD:5509061 20150910 MGI PMID:9674995 1621994 Ift56 intraflagellar transport 56 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20150910 MGI PMID:5088020 1621994 Ift56 intraflagellar transport 56 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20150910 MGI PMID:7317942 1621994 Ift56 intraflagellar transport 56 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20150910 MGI PMID:872193 1621994 Ift56 intraflagellar transport 56 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20151015 MGI PMID:25340710 1621994 Ift56 intraflagellar transport 56 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20150910 MGI PMID:5088020 1621994 Ift56 intraflagellar transport 56 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20150910 MGI PMID:5088020 1621994 Ift56 intraflagellar transport 56 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20150910 MGI PMID:5088020 1621994 Ift56 intraflagellar transport 56 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20150910 MGI PMID:9674995 1621994 Ift56 intraflagellar transport 56 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20151015 MGI PMID:25340710 1621994 Ift56 intraflagellar transport 56 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20151015 MGI PMID:5088020 1621994 Ift56 intraflagellar transport 56 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1621994 Ift56 intraflagellar transport 56 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20150910 MGI PMID:142347 1621994 Ift56 intraflagellar transport 56 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20150910 MGI PMID:7317942 1621994 Ift56 intraflagellar transport 56 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1621994 Ift56 intraflagellar transport 56 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20151015 MGI PMID:25340710 1621994 Ift56 intraflagellar transport 56 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20151015 MGI PMID:25340710 1621994 Ift56 intraflagellar transport 56 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20151015 MGI PMID:25340710 1621995 Prrt1 proline-rich transmembrane protein 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20180503 MGI PMID:29490264 1621995 Prrt1 proline-rich transmembrane protein 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20180503 MGI PMID:29490264 1621995 Prrt1 proline-rich transmembrane protein 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20180503 MGI PMID:29490264 1621995 Prrt1 proline-rich transmembrane protein 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20180503 MGI PMID:29490264 1621995 Prrt1 proline-rich transmembrane protein 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20180503 MGI PMID:29490264 1621996 Trim61 tripartite motif-containing 61 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1621996 Trim61 tripartite motif-containing 61 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1621996 Trim61 tripartite motif-containing 61 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1621996 Trim61 tripartite motif-containing 61 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20220811 MGI 1621996 Trim61 tripartite motif-containing 61 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1622022 Rbm47 RNA binding motif protein 47 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151126 MGI PMID:24916387 1622022 Rbm47 RNA binding motif protein 47 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151126 MGI PMID:24916387 1622022 Rbm47 RNA binding motif protein 47 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20151126 MGI PMID:24916387 1622022 Rbm47 RNA binding motif protein 47 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20151126 MGI PMID:24916387 1622022 Rbm47 RNA binding motif protein 47 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20151126 MGI PMID:24916387 1622024 Hephl1 hephaestin-like 1 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20190704 MGI PMID:5911159 1622024 Hephl1 hephaestin-like 1 gene MP:0000418 focal hair loss IEA N RGD:5509061 20190704 MGI 1622024 Hephl1 hephaestin-like 1 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20190704 MGI PMID:6092692 1622024 Hephl1 hephaestin-like 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20190704 MGI PMID:6092692 1622024 Hephl1 hephaestin-like 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20190704 MGI PMID:6092692 1622024 Hephl1 hephaestin-like 1 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20190704 MGI PMID:6092692 1622024 Hephl1 hephaestin-like 1 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20190704 MGI PMID:5911159 1622024 Hephl1 hephaestin-like 1 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20190704 MGI PMID:6092692 1622024 Hephl1 hephaestin-like 1 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20190808 MGI PMID:31293895 1622024 Hephl1 hephaestin-like 1 gene MP:0001279 wavy vibrissae IEA N RGD:5509061 20190704 MGI 1622024 Hephl1 hephaestin-like 1 gene MP:0001283 sparse vibrissae IEA N RGD:5509061 20190704 MGI 1622024 Hephl1 hephaestin-like 1 gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20190704 MGI 1622024 Hephl1 hephaestin-like 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20190704 MGI PMID:6092692 1622024 Hephl1 hephaestin-like 1 gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20190704 MGI PMID:5911159 1622024 Hephl1 hephaestin-like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20190704 MGI PMID:6092692 1622024 Hephl1 hephaestin-like 1 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20190704 MGI PMID:5911159 1622024 Hephl1 hephaestin-like 1 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20190704 MGI PMID:6092692 1622024 Hephl1 hephaestin-like 1 gene MP:0005409 darkened coat color IAGP N RGD:5509061 20190704 MGI PMID:5911159 1622024 Hephl1 hephaestin-like 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20190704 MGI PMID:6092692 1622025 Kdm4d lysine (K)-specific demethylase 4D gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:21293030 1622025 Kdm4d lysine (K)-specific demethylase 4D gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21293030 1622025 Kdm4d lysine (K)-specific demethylase 4D gene MP:0006308 enlarged seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:21293030 1622025 Kdm4d lysine (K)-specific demethylase 4D gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:21293030 1622025 Kdm4d lysine (K)-specific demethylase 4D gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21293030 1622026 Cntn5 contactin 5 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 1622026 Cntn5 contactin 5 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:12653969 1622026 Cntn5 contactin 5 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 1622026 Cntn5 contactin 5 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 1622027 Sprtn SprT-like N-terminal domain gene MP:0000160 kyphosis IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0000162 lordosis IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0001265 decreased body size IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0001304 cataract IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0003786 premature aging IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0005150 cachexia IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20210422 MGI PMID:32649882 1622027 Sprtn SprT-like N-terminal domain gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0009303 decreased renal fat pad weight IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622027 Sprtn SprT-like N-terminal domain gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20160407 MGI PMID:25501849 1622029 Gprin3 GPRIN family member 3 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20191024 MGI PMID:31363062 1622029 Gprin3 GPRIN family member 3 gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20191024 MGI PMID:31363062 1622029 Gprin3 GPRIN family member 3 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20191024 MGI PMID:31363062 1622029 Gprin3 GPRIN family member 3 gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20191024 MGI PMID:31363062 1622029 Gprin3 GPRIN family member 3 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20191024 MGI PMID:31363062 1622030 Aoc1l1 amine oxidase copper containing 1-like 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1622030 Aoc1l1 amine oxidase copper containing 1-like 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1622030 Aoc1l1 amine oxidase copper containing 1-like 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1622030 Aoc1l1 amine oxidase copper containing 1-like 1 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1622030 Aoc1l1 amine oxidase copper containing 1-like 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1622030 Aoc1l1 amine oxidase copper containing 1-like 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1622031 Gimap8 GTPase, IMAP family member 8 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 1622031 Gimap8 GTPase, IMAP family member 8 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1622037 Rxfp4 relaxin family peptide receptor 4 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220811 MGI 1622037 Rxfp4 relaxin family peptide receptor 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151008 MGI PMID:25028498 1622037 Rxfp4 relaxin family peptide receptor 4 gene MP:0001432 abnormal food preference IAGP N RGD:5509061 20151008 MGI PMID:25028498 1622037 Rxfp4 relaxin family peptide receptor 4 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 1622037 Rxfp4 relaxin family peptide receptor 4 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20151008 MGI PMID:25028498 1622037 Rxfp4 relaxin family peptide receptor 4 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20151008 MGI PMID:25028498 1622037 Rxfp4 relaxin family peptide receptor 4 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20151008 MGI PMID:25028498 1622037 Rxfp4 relaxin family peptide receptor 4 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20151008 MGI PMID:25028498 1622037 Rxfp4 relaxin family peptide receptor 4 gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20211021 MGI 1622037 Rxfp4 relaxin family peptide receptor 4 gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20151008 MGI PMID:25028498 1622037 Rxfp4 relaxin family peptide receptor 4 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1622039 Ankub1 ankyrin repeat and ubiquitin domain containing 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1622039 Ankub1 ankyrin repeat and ubiquitin domain containing 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1622039 Ankub1 ankyrin repeat and ubiquitin domain containing 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000022 abnormal ear shape IEA N RGD:5509061 20141003 MGI 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000372 irregular coat pigmentation IEA N RGD:5509061 20141003 MGI 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000445 short snout IEA N RGD:5509061 20111116 MGI 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:16880404 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20150319 MGI PMID:8055142 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:15838507 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000562 polydactyly IEA N RGD:5509061 20141003 MGI 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:15838507 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:16880404 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20150319 MGI PMID:8055142 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20200227 MGI PMID:30802441 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000576 clubfoot IAGP N RGD:5509061 20150319 MGI PMID:8055142 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20150319 MGI PMID:8055142 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20200227 MGI PMID:30802441 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20200227 MGI PMID:30802441 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0001340 abnormal eyelid morphology IEA N RGD:5509061 20141003 MGI 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20150319 MGI PMID:8055142 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20111116 MGI 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0001935 decreased litter size IEA N RGD:5509061 20141003 MGI 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20150319 MGI PMID:8055142 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200227 MGI PMID:30802441 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0002778 meroanencephaly IAGP N RGD:5509061 20150319 MGI PMID:8055142 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0003104 acrania IAGP N RGD:5509061 20150319 MGI PMID:8055142 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0003604 single kidney IAGP N RGD:5509061 20200227 MGI PMID:30802441 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20111116 MGI 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0003924 diaphragmatic hernia IEA N RGD:5509061 20150326 MGI 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0003935 abnormal craniofacial development IEA N RGD:5509061 20111116 MGI 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0004158 right aortic arch IEA N RGD:5509061 20150326 MGI 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0004222 iris synechia IAGP N RGD:5509061 20200227 MGI PMID:30802441 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20200227 MGI PMID:30802441 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0005242 cryptophthalmos IAGP N RGD:5509061 20141003 MGI PMID:15838507 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0005242 cryptophthalmos IAGP N RGD:5509061 20141003 MGI PMID:16880404 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0005242 cryptophthalmos IAGP N RGD:5509061 20200227 MGI PMID:30802441 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20200227 MGI PMID:30802441 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20200227 MGI PMID:30802441 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0008730 fused phalanges IEA N RGD:5509061 20141003 MGI 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0008854 bleb IAGP N RGD:5509061 20141003 MGI PMID:15838507 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0008854 bleb IAGP N RGD:5509061 20141003 MGI PMID:16880404 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0008855 eye bleb IEA N RGD:5509061 20111116 MGI 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0008856 fetal bleb IAGP N RGD:5509061 20141003 MGI PMID:15838507 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20150319 MGI PMID:8055142 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16087869 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0011090 perinatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15838507 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0011964 increased total retina thickness IAGP N RGD:5509061 20200227 MGI PMID:30802441 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0012101 acoria IAGP N RGD:5509061 20200227 MGI PMID:30802441 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0013742 absent ciliary body IAGP N RGD:5509061 20200227 MGI PMID:30802441 1622040 Frem2 Fras1 related extracellular matrix protein 2 gene MP:0030066 short face IEA N RGD:5509061 20170921 MGI 1622042 Kcnt2 potassium channel, subfamily T, member 2 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1622042 Kcnt2 potassium channel, subfamily T, member 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210826 MGI 1622042 Kcnt2 potassium channel, subfamily T, member 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20151119 MGI 1622042 Kcnt2 potassium channel, subfamily T, member 2 gene MP:0003488 decreased channel response intensity IAGP N RGD:5509061 20170921 MGI PMID:26559620 1622042 Kcnt2 potassium channel, subfamily T, member 2 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20170921 MGI PMID:26559620 1622042 Kcnt2 potassium channel, subfamily T, member 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20170921 MGI PMID:26559620 1622042 Kcnt2 potassium channel, subfamily T, member 2 gene MP:0008532 decreased chemical nociceptive threshold IAGP N RGD:5509061 20170921 MGI PMID:26559620 1622042 Kcnt2 potassium channel, subfamily T, member 2 gene MP:0009453 enhanced contextual conditioning behavior IEA N RGD:5509061 20231207 MGI 1622042 Kcnt2 potassium channel, subfamily T, member 2 gene MP:0010072 increased pruritus IAGP N RGD:5509061 20170921 MGI PMID:26559620 1622044 Fam83a family with sequence similarity 83, member A gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220811 MGI 1622045 Colec10 collectin sub-family member 10 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20181227 MGI 1622045 Colec10 collectin sub-family member 10 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 1622045 Colec10 collectin sub-family member 10 gene MP:0001258 decreased body length IEA N RGD:5509061 20181227 MGI 1622045 Colec10 collectin sub-family member 10 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1622045 Colec10 collectin sub-family member 10 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20230601 MGI 1622045 Colec10 collectin sub-family member 10 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1622045 Colec10 collectin sub-family member 10 gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 1622045 Colec10 collectin sub-family member 10 gene MP:0005270 abnormal zygomatic bone morphology IEA N RGD:5509061 20181227 MGI 1622046 Tmem74 transmembrane protein 74 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20181227 MGI 1622046 Tmem74 transmembrane protein 74 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1622046 Tmem74 transmembrane protein 74 gene MP:0000706 small thymus IEA N RGD:5509061 20220519 MGI 1622046 Tmem74 transmembrane protein 74 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20220519 MGI 1622046 Tmem74 transmembrane protein 74 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20210429 MGI PMID:30886335 1622046 Tmem74 transmembrane protein 74 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20210429 MGI PMID:30886335 1622046 Tmem74 transmembrane protein 74 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1622046 Tmem74 transmembrane protein 74 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1622046 Tmem74 transmembrane protein 74 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1622046 Tmem74 transmembrane protein 74 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20210429 MGI PMID:30886335 1622046 Tmem74 transmembrane protein 74 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20220519 MGI 1622046 Tmem74 transmembrane protein 74 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1622052 Magea10 MAGE family member A10 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20240509 MGI PMID:31149633 1622052 Magea10 MAGE family member A10 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20240509 MGI PMID:31149633 1622052 Magea10 MAGE family member A10 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20240509 MGI PMID:31149633 1622052 Magea10 MAGE family member A10 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240509 MGI PMID:31149633 1622052 Magea10 MAGE family member A10 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20240509 MGI PMID:31149633 1622056 Glyctk glycerate kinase gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20181227 MGI 1622056 Glyctk glycerate kinase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000141 abnormal vertebral body morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000297 abnormal atrioventricular cushion morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000562 polydactyly IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000692 small spleen IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000764 abnormal tongue epithelium morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000819 abnormal olfactory bulb morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000820 abnormal choroid plexus morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0001062 absent oculomotor nerve IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17481928 1622060 B9d2 B9 protein domain 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:21435587 1622060 B9d2 B9 protein domain 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:21435587 1622060 B9d2 B9 protein domain 2 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21435587 1622060 B9d2 B9 protein domain 2 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0002239 abnormal nasal septum morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0002279 abnormal diaphragm morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:21435587 1622060 B9d2 B9 protein domain 2 gene MP:0002947 increased hemangioma incidence IEA N RGD:5509061 20210930 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0003078 aphakia IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0003178 left pulmonary isomerism IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0003262 intestinal/bowel diverticulum IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0003342 accessory spleen IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0003584 bifid ureter IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0004110 transposition of great arteries IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0004133 heterotaxia IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0004163 abnormal adenohypophysis morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0004164 abnormal neurohypophysis morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0004247 small pancreas IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0004790 absent upper incisors IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21435587 1622060 B9d2 B9 protein domain 2 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23645881 1622060 B9d2 B9 protein domain 2 gene MP:0004950 abnormal brain vasculature morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21435587 1622060 B9d2 B9 protein domain 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:21435587 1622060 B9d2 B9 protein domain 2 gene MP:0005358 abnormal incisor morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0006065 abnormal heart position or orientation IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:21435587 1622060 B9d2 B9 protein domain 2 gene MP:0008119 decreased Langerhans cell number IAGP N RGD:5509061 20141003 MGI PMID:17938236 1622060 B9d2 B9 protein domain 2 gene MP:0008128 abnormal brain internal capsule morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0008320 absent adenohypophysis IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21435587 1622060 B9d2 B9 protein domain 2 gene MP:0008923 thoracoschisis IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0009770 abnormal optic chiasm morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0010200 enlarged lymphatic vessel IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:21435587 1622060 B9d2 B9 protein domain 2 gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21435587 1622060 B9d2 B9 protein domain 2 gene MP:0010406 common atrium IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0010427 double outlet left ventricle IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0010433 double inlet heart left ventricle IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0010439 abnormal hepatic vein morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0010440 anomalous pulmonary venous connection IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0010496 abnormal pectinate muscle morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0010526 aortic arch coarctation IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0010527 bicuspid pulmonary valve IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0010572 persistent right dorsal aorta IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0010614 abnormal mitral valve cusp morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0011250 abdominal situs ambiguus IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0011380 enlarged brain ventricles IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0011493 double ureter IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0011513 abnormal vertebral artery morphology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0011727 ectopic ovary IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013823 absent segment of anterior cerebral artery IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013827 thin oculomotor nerve IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013830 abnormal intrathoracic topology of vagus nerve IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013842 ductus venosus stenosis IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013874 abnormal ductus venosus topology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013878 abnormal ductus venosus valve topology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013917 persistent right 6th pharyngeal arch artery IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013928 thin motoric part of trigeminal nerve IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013936 abnormal thymus topology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013977 symmetric azygos veins IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013979 abnormal subclavian artery origin IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013982 inverse situs of great intrathoracic arteries IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013985 abnormal umbilical vein topology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0013987 absent intrahepatic inferior vena cava segment IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0014000 anastomosis between internal carotid artery and basilar artery IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0014003 additional anastomosis between intracranial vertebral arteries IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0014017 abnormal Wolffian duct connection IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0014018 embryo tumor IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0014019 embryo cyst IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0014023 abnormal intestine placement IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0020301 short tongue IEA N RGD:5509061 20180628 MGI 1622060 B9d2 B9 protein domain 2 gene MP:0020494 left sided inferior vena cava IEA N RGD:5509061 20180628 MGI 1622063 Lypd4 Ly6/Plaur domain containing 4 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20230413 MGI PMID:32040177 1622063 Lypd4 Ly6/Plaur domain containing 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20230413 MGI PMID:32040177 1622063 Lypd4 Ly6/Plaur domain containing 4 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20230413 MGI PMID:32040177 1622063 Lypd4 Ly6/Plaur domain containing 4 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20230413 MGI PMID:32040177 1622063 Lypd4 Ly6/Plaur domain containing 4 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20230413 MGI PMID:32040177 1622063 Lypd4 Ly6/Plaur domain containing 4 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20230413 MGI PMID:32040177 1622070 Ppm1n protein phosphatase, Mg2+/Mn2+ dependent, 1N (putative) gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1622070 Ppm1n protein phosphatase, Mg2+/Mn2+ dependent, 1N (putative) gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1622070 Ppm1n protein phosphatase, Mg2+/Mn2+ dependent, 1N (putative) gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1622070 Ppm1n protein phosphatase, Mg2+/Mn2+ dependent, 1N (putative) gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1622070 Ppm1n protein phosphatase, Mg2+/Mn2+ dependent, 1N (putative) gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20160915 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:11283609 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0000914 exencephaly IAGP N RGD:5509061 20160915 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0000923 abnormal roof plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11283609 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11283609 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11283609 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11283609 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11283609 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11283609 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20111116 MGI 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0002081 perinatal lethality IEA N RGD:5509061 20111116 MGI 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20111116 MGI 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20160915 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:11283609 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0003054 spina bifida IAGP N RGD:5509061 20160915 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20160915 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0003604 single kidney IAGP N RGD:5509061 20160915 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0003670 dilated renal glomerular capsule IAGP N RGD:5509061 20160915 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20160915 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0003861 abnormal nervous system development IEA N RGD:5509061 20111116 MGI 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0005549 retina pigment epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20160915 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0010860 abnormal anterior commissure pars posterior morphology IAGP N RGD:5509061 20141003 MGI PMID:11283609 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20160915 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160915 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20160915 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20160915 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20160915 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0012026 abnormal S-shaped body morphology IAGP N RGD:5509061 20160915 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0012535 abnormal optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:11044403 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:26859289 1622073 Arhgap35 Rho GTPase activating protein 35 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:11044403 1622074 Vsig10 V-set and immunoglobulin domain containing 10 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1622075 Myo1h myosin 1H gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20190502 MGI 1622075 Myo1h myosin 1H gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1622075 Myo1h myosin 1H gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1622075 Myo1h myosin 1H gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622075 Myo1h myosin 1H gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20211021 MGI 1622076 Ssh1 slingshot protein phosphatase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1622077 Ficd FIC domain containing gene MP:0000452 abnormal mouth morphology IEA N RGD:5509061 20201022 MGI 1622077 Ficd FIC domain containing gene MP:0001284 absent vibrissae IEA N RGD:5509061 20181227 MGI 1622077 Ficd FIC domain containing gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1622077 Ficd FIC domain containing gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20221215 MGI 1622080 Acer2 alkaline ceramidase 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20180301 MGI PMID:29056331 1622080 Acer2 alkaline ceramidase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180301 MGI PMID:29401619 1622080 Acer2 alkaline ceramidase 2 gene MP:0012230 abnormal sphingolipid level IAGP N RGD:5509061 20180301 MGI PMID:29401619 1622081 Haus6 HAUS augmin-like complex, subunit 6 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20180308 MGI PMID:27052165 1622081 Haus6 HAUS augmin-like complex, subunit 6 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20180308 MGI PMID:27052165 1622081 Haus6 HAUS augmin-like complex, subunit 6 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180308 MGI PMID:27052165 1622083 Cfap157 cilia and flagella associated protein 157 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20180111 MGI PMID:27965440 1622083 Cfap157 cilia and flagella associated protein 157 gene MP:0001925 male infertility IAGP N RGD:5509061 20180111 MGI PMID:27965440 1622083 Cfap157 cilia and flagella associated protein 157 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20180111 MGI PMID:27965440 1622083 Cfap157 cilia and flagella associated protein 157 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20180111 MGI PMID:27965440 1622083 Cfap157 cilia and flagella associated protein 157 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20180111 MGI PMID:27965440 1622083 Cfap157 cilia and flagella associated protein 157 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20180111 MGI PMID:27965440 1622083 Cfap157 cilia and flagella associated protein 157 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20180111 MGI PMID:27965440 1622083 Cfap157 cilia and flagella associated protein 157 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20180111 MGI PMID:27965440 1622083 Cfap157 cilia and flagella associated protein 157 gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20180111 MGI PMID:27965440 1622083 Cfap157 cilia and flagella associated protein 157 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20180111 MGI PMID:27965440 1622085 Nup214 nucleoporin 214 gene MP:0004963 abnormal blastocoele morphology IAGP N RGD:5509061 20141003 MGI PMID:8896451 1622085 Nup214 nucleoporin 214 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8896451 1622086 Qrfp pyroglutamylated RFamide peptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180809 MGI PMID:27835635 1622086 Qrfp pyroglutamylated RFamide peptide gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20180809 MGI PMID:27835635 1622086 Qrfp pyroglutamylated RFamide peptide gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180809 MGI PMID:27835635 1622086 Qrfp pyroglutamylated RFamide peptide gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20180809 MGI PMID:27835635 1622086 Qrfp pyroglutamylated RFamide peptide gene MP:0003064 decreased coping response IAGP N RGD:5509061 20180809 MGI PMID:27835635 1622086 Qrfp pyroglutamylated RFamide peptide gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20180809 MGI PMID:27835635 1622086 Qrfp pyroglutamylated RFamide peptide gene MP:0011940 decreased food intake IAGP N RGD:5509061 20180809 MGI PMID:27835635 1622086 Qrfp pyroglutamylated RFamide peptide gene MP:0012289 abnormal non-rapid eye movement sleep pattern IAGP N RGD:5509061 20180809 MGI PMID:27835635 1622086 Qrfp pyroglutamylated RFamide peptide gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20180809 MGI PMID:27835635 1622086 Qrfp pyroglutamylated RFamide peptide gene MP:0020478 abnormal circadian sleep/wake cycle IAGP N RGD:5509061 20180809 MGI PMID:27835635 1622088 Ascl5 achaete-scute family bHLH transcription factor 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1622088 Ascl5 achaete-scute family bHLH transcription factor 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1622088 Ascl5 achaete-scute family bHLH transcription factor 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1622088 Ascl5 achaete-scute family bHLH transcription factor 5 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1622088 Ascl5 achaete-scute family bHLH transcription factor 5 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1622088 Ascl5 achaete-scute family bHLH transcription factor 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1622088 Ascl5 achaete-scute family bHLH transcription factor 5 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230601 MGI 1622088 Ascl5 achaete-scute family bHLH transcription factor 5 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20230601 MGI 1622089 Igfn1 immunoglobulin-like and fibronectin type III domain containing 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240307 MGI PMID:37572089 1622090 R3hdm1 R3H domain containing 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200310 MGI 1622090 R3hdm1 R3H domain containing 1 gene MP:0001147 small testis IEA N RGD:5509061 20200310 MGI 1622090 R3hdm1 R3H domain containing 1 gene MP:0003049 abnormal lumbar vertebrae morphology IEA N RGD:5509061 20220811 MGI 1622090 R3hdm1 R3H domain containing 1 gene MP:0003050 abnormal sacral vertebrae morphology IEA N RGD:5509061 20220811 MGI 1622091 Rbbp8 retinoblastoma binding protein 8, endonuclease gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20200310 MGI PMID:15831459 1622091 Rbbp8 retinoblastoma binding protein 8, endonuclease gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:15831459 1622091 Rbbp8 retinoblastoma binding protein 8, endonuclease gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:15831459 1622091 Rbbp8 retinoblastoma binding protein 8, endonuclease gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20200310 MGI PMID:15831459 1622091 Rbbp8 retinoblastoma binding protein 8, endonuclease gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15831459 1622091 Rbbp8 retinoblastoma binding protein 8, endonuclease gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:15831459 1622091 Rbbp8 retinoblastoma binding protein 8, endonuclease gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:15831459 1622092 Pphln1 periphilin 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19621438 1622093 Gxylt1 glucoside xylosyltransferase 1 gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20201022 MGI 1622093 Gxylt1 glucoside xylosyltransferase 1 gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1622093 Gxylt1 glucoside xylosyltransferase 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1622093 Gxylt1 glucoside xylosyltransferase 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 1622093 Gxylt1 glucoside xylosyltransferase 1 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20201022 MGI 1622093 Gxylt1 glucoside xylosyltransferase 1 gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20201022 MGI 1622093 Gxylt1 glucoside xylosyltransferase 1 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20201022 MGI 1622093 Gxylt1 glucoside xylosyltransferase 1 gene MP:0003896 prolonged PR interval IEA N RGD:5509061 20211021 MGI 1622093 Gxylt1 glucoside xylosyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1622093 Gxylt1 glucoside xylosyltransferase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1622093 Gxylt1 glucoside xylosyltransferase 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1622097 Ccno cyclin O gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20160929 MGI PMID:25712475 1622097 Ccno cyclin O gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1622097 Ccno cyclin O gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1622097 Ccno cyclin O gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160929 MGI PMID:25712475 1622097 Ccno cyclin O gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20160929 MGI PMID:25712475 1622097 Ccno cyclin O gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1622097 Ccno cyclin O gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20160929 MGI PMID:25712475 1622097 Ccno cyclin O gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1622097 Ccno cyclin O gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20160929 MGI PMID:25712475 1622097 Ccno cyclin O gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20160929 MGI PMID:25712475 1622097 Ccno cyclin O gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20160929 MGI PMID:25712475 1622097 Ccno cyclin O gene MP:0031101 nasal obstruction IAGP N RGD:5509061 20201015 MGI PMID:25712475 1622098 Il31ra interleukin 31 receptor A gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17379091 1622098 Il31ra interleukin 31 receptor A gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17379091 1622098 Il31ra interleukin 31 receptor A gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:17379091 1622098 Il31ra interleukin 31 receptor A gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17353366 1622098 Il31ra interleukin 31 receptor A gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:17353366 1622098 Il31ra interleukin 31 receptor A gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:17353366 1622098 Il31ra interleukin 31 receptor A gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 1622098 Il31ra interleukin 31 receptor A gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17353366 1622098 Il31ra interleukin 31 receptor A gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17353366 1622098 Il31ra interleukin 31 receptor A gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17379091 1622098 Il31ra interleukin 31 receptor A gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:17353366 1622098 Il31ra interleukin 31 receptor A gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 1622098 Il31ra interleukin 31 receptor A gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20170105 MGI 1622099 Cybc1 cytochrome b 245 chaperone 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1622099 Cybc1 cytochrome b 245 chaperone 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160804 MGI 1622099 Cybc1 cytochrome b 245 chaperone 1 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20160804 MGI 1622099 Cybc1 cytochrome b 245 chaperone 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160804 MGI 1622099 Cybc1 cytochrome b 245 chaperone 1 gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20160804 MGI 1622099 Cybc1 cytochrome b 245 chaperone 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 1622099 Cybc1 cytochrome b 245 chaperone 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160804 MGI 1622101 Tmc8 transmembrane channel-like gene family 8 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20210506 MGI PMID:32917726 1622101 Tmc8 transmembrane channel-like gene family 8 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20210506 MGI PMID:32917726 1622101 Tmc8 transmembrane channel-like gene family 8 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20210506 MGI PMID:32917726 1622102 Tmc6 transmembrane channel-like gene family 6 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1622102 Tmc6 transmembrane channel-like gene family 6 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20201231 MGI 1622102 Tmc6 transmembrane channel-like gene family 6 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 1622102 Tmc6 transmembrane channel-like gene family 6 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20210506 MGI PMID:32917726 1622102 Tmc6 transmembrane channel-like gene family 6 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20210506 MGI PMID:32917726 1622102 Tmc6 transmembrane channel-like gene family 6 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20210506 MGI PMID:32917726 1622103 Qrich2 glutamine rich 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20190912 MGI PMID:30683861 1622103 Qrich2 glutamine rich 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20190912 MGI PMID:30683861 1622103 Qrich2 glutamine rich 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20190912 MGI PMID:30683861 1622103 Qrich2 glutamine rich 2 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20190912 MGI PMID:30683861 1622103 Qrich2 glutamine rich 2 gene MP:0004930 small epididymis IAGP N RGD:5509061 20190912 MGI PMID:30683861 1622103 Qrich2 glutamine rich 2 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20190912 MGI PMID:30683861 1622103 Qrich2 glutamine rich 2 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20190912 MGI PMID:30683861 1622103 Qrich2 glutamine rich 2 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20190912 MGI PMID:30683861 1622103 Qrich2 glutamine rich 2 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20190912 MGI PMID:30683861 1622103 Qrich2 glutamine rich 2 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20190912 MGI PMID:30683861 1622103 Qrich2 glutamine rich 2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20190912 MGI PMID:30683861 1622103 Qrich2 glutamine rich 2 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20190912 MGI PMID:30683861 1622103 Qrich2 glutamine rich 2 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20190912 MGI PMID:30683861 1622103 Qrich2 glutamine rich 2 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20190912 MGI PMID:30683861 1622103 Qrich2 glutamine rich 2 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220317 MGI PMID:30683861 1622104 Fbf1 Fas binding factor 1 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20211021 MGI 1622104 Fbf1 Fas binding factor 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20200402 MGI 1622104 Fbf1 Fas binding factor 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1622104 Fbf1 Fas binding factor 1 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1622104 Fbf1 Fas binding factor 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1622104 Fbf1 Fas binding factor 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201022 MGI 1622104 Fbf1 Fas binding factor 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1622104 Fbf1 Fas binding factor 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200310 MGI 1622104 Fbf1 Fas binding factor 1 gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20200310 MGI 1622104 Fbf1 Fas binding factor 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20200310 MGI 1622104 Fbf1 Fas binding factor 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1622104 Fbf1 Fas binding factor 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1622104 Fbf1 Fas binding factor 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1622107 Cd300ld CD300 molecule like family member d gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1622108 Gpr142 G protein-coupled receptor 142 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20210422 MGI PMID:27322810 1622108 Gpr142 G protein-coupled receptor 142 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20210422 MGI PMID:27322810 1622108 Gpr142 G protein-coupled receptor 142 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20210422 MGI PMID:27322810 1622108 Gpr142 G protein-coupled receptor 142 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220811 MGI 1622108 Gpr142 G protein-coupled receptor 142 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20221215 MGI 1622108 Gpr142 G protein-coupled receptor 142 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20210422 MGI PMID:27322810 1622108 Gpr142 G protein-coupled receptor 142 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20210422 MGI PMID:27322810 1622108 Gpr142 G protein-coupled receptor 142 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20210422 MGI PMID:27322810 1622108 Gpr142 G protein-coupled receptor 142 gene MP:0020151 abnormal circulating non-HDL cholesterol level IAGP N RGD:5509061 20210422 MGI PMID:27322810 1622110 Ctnna3 catenin alpha 3 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:22421363 1622110 Ctnna3 catenin alpha 3 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20200310 MGI PMID:22421363 1622110 Ctnna3 catenin alpha 3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20200310 MGI PMID:22421363 1622110 Ctnna3 catenin alpha 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20200310 MGI PMID:22421363 1622110 Ctnna3 catenin alpha 3 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20200310 MGI PMID:22421363 1622110 Ctnna3 catenin alpha 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20200310 MGI PMID:22421363 1622110 Ctnna3 catenin alpha 3 gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20200310 MGI PMID:22421363 1622110 Ctnna3 catenin alpha 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200310 MGI PMID:22421363 1622111 Stox1 storkhead box 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20220825 MGI PMID:33301424 1622111 Stox1 storkhead box 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20220825 MGI PMID:33301424 1622111 Stox1 storkhead box 1 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20220825 MGI PMID:33301424 1622111 Stox1 storkhead box 1 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20220825 MGI PMID:33301424 1622111 Stox1 storkhead box 1 gene MP:0010038 abnormal placenta physiology IAGP N RGD:5509061 20220825 MGI PMID:33301424 1622111 Stox1 storkhead box 1 gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20220825 MGI PMID:33301424 1622111 Stox1 storkhead box 1 gene MP:0012045 increased susceptibility to hypertension IAGP N RGD:5509061 20220825 MGI PMID:33301424 1622112 Hkdc1 hexokinase domain containing 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1622112 Hkdc1 hexokinase domain containing 1 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20200130 MGI PMID:30085091 1622112 Hkdc1 hexokinase domain containing 1 gene MP:0003926 decreased cellular glucose uptake IAGP N RGD:5509061 20230119 MGI PMID:27459389 1622112 Hkdc1 hexokinase domain containing 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20231207 MGI 1622112 Hkdc1 hexokinase domain containing 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20171116 MGI PMID:27459389 1622112 Hkdc1 hexokinase domain containing 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200130 MGI PMID:30085091 1622112 Hkdc1 hexokinase domain containing 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200130 MGI PMID:30085091 1622112 Hkdc1 hexokinase domain containing 1 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200130 MGI PMID:30085091 1622112 Hkdc1 hexokinase domain containing 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20230119 MGI PMID:27459389 1622112 Hkdc1 hexokinase domain containing 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20231207 MGI 1622112 Hkdc1 hexokinase domain containing 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 1622112 Hkdc1 hexokinase domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20171116 MGI PMID:27459389 1622112 Hkdc1 hexokinase domain containing 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200130 MGI PMID:30085091 1622112 Hkdc1 hexokinase domain containing 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200130 MGI PMID:30085091 1622113 Cgas cyclic GMP-AMP synthase gene MP:0001391 abnormal tail movements IEA N RGD:5509061 20160804 MGI 1622113 Cgas cyclic GMP-AMP synthase gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23989956 1622113 Cgas cyclic GMP-AMP synthase gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23989956 1622113 Cgas cyclic GMP-AMP synthase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:23989956 1622113 Cgas cyclic GMP-AMP synthase gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20231026 MGI PMID:37532932 1622113 Cgas cyclic GMP-AMP synthase gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1622113 Cgas cyclic GMP-AMP synthase gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20160915 MGI PMID:27496731 1622113 Cgas cyclic GMP-AMP synthase gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:23989956 1622113 Cgas cyclic GMP-AMP synthase gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20141003 MGI PMID:23989956 1622113 Cgas cyclic GMP-AMP synthase gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23989956 1622113 Cgas cyclic GMP-AMP synthase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160804 MGI 1622113 Cgas cyclic GMP-AMP synthase gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20231026 MGI PMID:37532932 1622113 Cgas cyclic GMP-AMP synthase gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:23989956 1622113 Cgas cyclic GMP-AMP synthase gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:24284630 1622113 Cgas cyclic GMP-AMP synthase gene MP:0020928 increased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:24284630 1622113 Cgas cyclic GMP-AMP synthase gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:27496731 1622113 Cgas cyclic GMP-AMP synthase gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:29871919 1622113 Cgas cyclic GMP-AMP synthase gene MP:0020943 increased susceptibility to Flaviviridae infection IAGP N RGD:5509061 20200430 MGI PMID:24284630 1622113 Cgas cyclic GMP-AMP synthase gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:23989956 1622113 Cgas cyclic GMP-AMP synthase gene MP:0031034 increased susceptibility to Poxviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:24284630 1622113 Cgas cyclic GMP-AMP synthase gene MP:0031044 increased susceptibility to Flaviviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:24284630 1622114 Rcor3 REST corepressor 3 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220519 MGI 1622114 Rcor3 REST corepressor 3 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 1622114 Rcor3 REST corepressor 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1622116 Iqub IQ motif and ubiquitin domain containing gene MP:0001925 male infertility IAGP N RGD:5509061 20230112 MGI PMID:36417862 1622116 Iqub IQ motif and ubiquitin domain containing gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230112 MGI PMID:36417862 1622116 Iqub IQ motif and ubiquitin domain containing gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20230112 MGI PMID:36417862 1622116 Iqub IQ motif and ubiquitin domain containing gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20230112 MGI PMID:36417862 1622116 Iqub IQ motif and ubiquitin domain containing gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20230112 MGI PMID:36417862 1622120 Gpr174 G protein-coupled receptor 174 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20150730 MGI PMID:26077720 1622120 Gpr174 G protein-coupled receptor 174 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20150730 MGI PMID:26077720 1622120 Gpr174 G protein-coupled receptor 174 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20150730 MGI PMID:26077720 1622120 Gpr174 G protein-coupled receptor 174 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20150730 MGI PMID:26077720 1622120 Gpr174 G protein-coupled receptor 174 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20150730 MGI PMID:26077720 1622121 Rtl3 retrotransposon Gag like 3 gene MP:0005655 increased aggression IEA N RGD:5509061 20201022 MGI 1622121 Rtl3 retrotransposon Gag like 3 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 1622123 Armc2 armadillo repeat containing 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1622123 Armc2 armadillo repeat containing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20191128 MGI PMID:30686508 1622123 Armc2 armadillo repeat containing 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20191128 MGI PMID:30686508 1622123 Armc2 armadillo repeat containing 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1622123 Armc2 armadillo repeat containing 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1622123 Armc2 armadillo repeat containing 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1622123 Armc2 armadillo repeat containing 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20191128 MGI PMID:30686508 1622123 Armc2 armadillo repeat containing 2 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20191128 MGI PMID:30686508 1622123 Armc2 armadillo repeat containing 2 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20191128 MGI PMID:30686508 1622123 Armc2 armadillo repeat containing 2 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20191128 MGI PMID:30686508 1622123 Armc2 armadillo repeat containing 2 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20191128 MGI PMID:30686508 1622123 Armc2 armadillo repeat containing 2 gene MP:0009241 thick sperm flagellum IAGP N RGD:5509061 20191128 MGI PMID:30686508 1622123 Armc2 armadillo repeat containing 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20190502 MGI 1622123 Armc2 armadillo repeat containing 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622123 Armc2 armadillo repeat containing 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1622123 Armc2 armadillo repeat containing 2 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20191128 MGI PMID:30686508 1622123 Armc2 armadillo repeat containing 2 gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20220317 MGI PMID:30686508 1622124 Wdr25 WD repeat domain 25 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20240926 MGI 1622124 Wdr25 WD repeat domain 25 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20240926 MGI 1622124 Wdr25 WD repeat domain 25 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20240926 MGI 1622124 Wdr25 WD repeat domain 25 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20240926 MGI 1622124 Wdr25 WD repeat domain 25 gene MP:0009331 absent primitive node IEA N RGD:5509061 20240926 MGI 1622124 Wdr25 WD repeat domain 25 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1622124 Wdr25 WD repeat domain 25 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 1622124 Wdr25 WD repeat domain 25 gene MP:0012724 absent head fold IEA N RGD:5509061 20240926 MGI 1622124 Wdr25 WD repeat domain 25 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1622125 Ccdc191 coiled-coil domain containing 191 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1622125 Ccdc191 coiled-coil domain containing 191 gene MP:0002546 mydriasis IEA N RGD:5509061 20190502 MGI 1622129 Il23r interleukin 23 receptor gene MP:0001263 weight loss IAGP N RGD:5509061 20151112 MGI PMID:22089030 1622129 Il23r interleukin 23 receptor gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1622129 Il23r interleukin 23 receptor gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23034650 1622129 Il23r interleukin 23 receptor gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17074928 1622129 Il23r interleukin 23 receptor gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:19414740 1622129 Il23r interleukin 23 receptor gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20151112 MGI PMID:22089030 1622129 Il23r interleukin 23 receptor gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19414740 1622129 Il23r interleukin 23 receptor gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19433802 1622129 Il23r interleukin 23 receptor gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19414740 1622129 Il23r interleukin 23 receptor gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20151112 MGI PMID:22089030 1622129 Il23r interleukin 23 receptor gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20151112 MGI PMID:22089030 1622129 Il23r interleukin 23 receptor gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20151112 MGI PMID:22089030 1622129 Il23r interleukin 23 receptor gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20151112 MGI PMID:22089030 1622129 Il23r interleukin 23 receptor gene MP:0008712 decreased interleukin-9 secretion IAGP N RGD:5509061 20141003 MGI PMID:19433802 1622129 Il23r interleukin 23 receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20151112 MGI PMID:22089030 1622129 Il23r interleukin 23 receptor gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:22089030 1622131 Nudcd3 NudC domain containing 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0001924 infertility IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1622131 Nudcd3 NudC domain containing 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1622131 Nudcd3 NudC domain containing 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210520 MGI 1622131 Nudcd3 NudC domain containing 3 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210520 MGI 1622131 Nudcd3 NudC domain containing 3 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0008761 abnormal immunoglobulin light chain V-J recombination IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1622131 Nudcd3 NudC domain containing 3 gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622131 Nudcd3 NudC domain containing 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240808 MGI PMID:38787962 1622132 Rad51ap2 RAD51 associated protein 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220331 MGI PMID:35020426 1622132 Rad51ap2 RAD51 associated protein 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220331 MGI PMID:35020426 1622132 Rad51ap2 RAD51 associated protein 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20220331 MGI PMID:35020426 1622132 Rad51ap2 RAD51 associated protein 2 gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20220331 MGI PMID:35020426 1622132 Rad51ap2 RAD51 associated protein 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220331 MGI PMID:35020426 1622133 Rtl9 retrotransposon Gag like 9 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20240118 MGI PMID:37834332 1622136 Tor1aip1 torsin A interacting protein 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20240328 MGI PMID:38194265 1622136 Tor1aip1 torsin A interacting protein 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20240328 MGI PMID:38194265 1622136 Tor1aip1 torsin A interacting protein 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20240328 MGI PMID:38194265 1622136 Tor1aip1 torsin A interacting protein 1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:20457914 1622136 Tor1aip1 torsin A interacting protein 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20457914 1622136 Tor1aip1 torsin A interacting protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622141 Zfp469 zinc finger protein 469 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1622141 Zfp469 zinc finger protein 469 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20211021 MGI PMID:34368841 1622141 Zfp469 zinc finger protein 469 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20211021 MGI PMID:34368841 1622141 Zfp469 zinc finger protein 469 gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 1622141 Zfp469 zinc finger protein 469 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20211021 MGI PMID:34368841 1622141 Zfp469 zinc finger protein 469 gene MP:0001265 decreased body size IAGP N RGD:5509061 20211021 MGI PMID:34368841 1622141 Zfp469 zinc finger protein 469 gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 1622141 Zfp469 zinc finger protein 469 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20211021 MGI PMID:34368841 1622141 Zfp469 zinc finger protein 469 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210520 MGI 1622141 Zfp469 zinc finger protein 469 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1622141 Zfp469 zinc finger protein 469 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 1622141 Zfp469 zinc finger protein 469 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20211021 MGI PMID:34368841 1622141 Zfp469 zinc finger protein 469 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1622141 Zfp469 zinc finger protein 469 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1622141 Zfp469 zinc finger protein 469 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20211021 MGI PMID:34368841 1622141 Zfp469 zinc finger protein 469 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1622141 Zfp469 zinc finger protein 469 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1622141 Zfp469 zinc finger protein 469 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20211021 MGI PMID:34368841 1622141 Zfp469 zinc finger protein 469 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20211021 MGI PMID:34368841 1622141 Zfp469 zinc finger protein 469 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20211021 MGI PMID:34368841 1622141 Zfp469 zinc finger protein 469 gene MP:0009827 skin detachment IAGP N RGD:5509061 20211021 MGI PMID:34368841 1622141 Zfp469 zinc finger protein 469 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1622141 Zfp469 zinc finger protein 469 gene MP:0011650 abnormal cornea stroma collagen fibril morphology IAGP N RGD:5509061 20211021 MGI PMID:34368841 1622141 Zfp469 zinc finger protein 469 gene MP:0020860 abnormal cornea physiology IAGP N RGD:5509061 20211021 MGI PMID:34368841 1622141 Zfp469 zinc finger protein 469 gene MP:0031213 increased eye anterior chamber depth IAGP N RGD:5509061 20211021 MGI PMID:34368841 1622142 Dcdc2a doublecortin domain containing 2a gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21883923 1622142 Dcdc2a doublecortin domain containing 2a gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:21883923 1622142 Dcdc2a doublecortin domain containing 2a gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:21883923 1622142 Dcdc2a doublecortin domain containing 2a gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:21883923 1622145 Selenom selenoprotein M gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23880772 1622145 Selenom selenoprotein M gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:23880772 1622145 Selenom selenoprotein M gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23880772 1622145 Selenom selenoprotein M gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:23880772 1622145 Selenom selenoprotein M gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:23880772 1622145 Selenom selenoprotein M gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23880772 1622145 Selenom selenoprotein M gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23880772 1622145 Selenom selenoprotein M gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23880772 1622149 Ly6g6d lymphocyte antigen 6 family member G6D gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1622149 Ly6g6d lymphocyte antigen 6 family member G6D gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 1622149 Ly6g6d lymphocyte antigen 6 family member G6D gene MP:0002834 decreased heart weight IEA N RGD:5509061 20181227 MGI 1622149 Ly6g6d lymphocyte antigen 6 family member G6D gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20181227 MGI 1622149 Ly6g6d lymphocyte antigen 6 family member G6D gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210520 MGI 1622149 Ly6g6d lymphocyte antigen 6 family member G6D gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20210520 MGI 1622151 Pth2 parathyroid hormone 2 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18483145 1622151 Pth2 parathyroid hormone 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:18483145 1622151 Pth2 parathyroid hormone 2 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18483145 1622151 Pth2 parathyroid hormone 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:18483145 1622151 Pth2 parathyroid hormone 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18483145 1622151 Pth2 parathyroid hormone 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:18483145 1622151 Pth2 parathyroid hormone 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18483145 1622151 Pth2 parathyroid hormone 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18483145 1622151 Pth2 parathyroid hormone 2 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:18483145 1622151 Pth2 parathyroid hormone 2 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18483145 1622151 Pth2 parathyroid hormone 2 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:18483145 1622151 Pth2 parathyroid hormone 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18483145 1622151 Pth2 parathyroid hormone 2 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:18483145 1622151 Pth2 parathyroid hormone 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:18483145 1622152 Elac1 elaC ribonuclease Z 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21937600 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0001577 anemia IAGP N RGD:5509061 20180531 MGI PMID:26833786 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0002237 abnormal nasal cavity morphology IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0002239 abnormal nasal septum morphology IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0002652 thin myocardium IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0002928 abnormal bile duct morphology IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0003078 aphakia IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0005262 coloboma IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0008109 abnormal small intestinal microvillus morphology IAGP N RGD:5509061 20180531 MGI PMID:26833786 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0008141 decreased small intestinal microvillus size IAGP N RGD:5509061 20180531 MGI PMID:26833786 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0009493 abnormal cystic duct morphology IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0009770 abnormal optic chiasm morphology IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0009907 decreased tongue size IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0010595 abnormal aortic valve cusp morphology IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180531 MGI PMID:26833786 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0013833 absent olfactory nerve IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0013852 abnormal Mullerian duct topology IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0013855 absent celiac artery IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0013875 increased trigeminal neuroma incidence IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0014003 additional anastomosis between intracranial vertebral arteries IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0014018 embryo tumor IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0014087 retrolental blood IEA N RGD:5509061 20180830 MGI 1622154 Ehbp1l1 EH domain binding protein 1-like 1 gene MP:0030474 fused incisors IEA N RGD:5509061 20180830 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0000111 cleft palate IEA N RGD:5509061 20141003 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20141003 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20141003 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0000276 heart right ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20210826 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0000445 short snout IEA N RGD:5509061 20141003 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20141003 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0001304 cataract IEA N RGD:5509061 20210520 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20230601 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0001625 cardiac hypertrophy IEA N RGD:5509061 20150827 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210826 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0001785 edema IEA N RGD:5509061 20210826 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20141003 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20230601 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0002192 hydrops fetalis IEA N RGD:5509061 20141003 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0002625 heart left ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210826 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0010082 sternebra fusion IEA N RGD:5509061 20150827 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141003 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20141003 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20141003 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20230601 MGI 1622161 Adamts6 ADAM metallopeptidase with thrombospondin type 1 motif 6 gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20190131 MGI PMID:30322915 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20190131 MGI PMID:30322915 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0001314 cornea opacity IEA N RGD:5509061 20220811 MGI 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20220811 MGI 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0001577 anemia IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20220811 MGI 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0002083 premature death IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20190131 MGI PMID:30322915 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20190131 MGI PMID:30322915 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20190131 MGI PMID:30322915 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20190131 MGI PMID:30322915 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20190131 MGI PMID:30322915 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20190131 MGI PMID:30322915 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20190131 MGI PMID:30322915 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20190131 MGI PMID:30322915 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20190131 MGI PMID:30322915 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230601 MGI 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0013657 abnormal blood cell morphology IAGP N RGD:5509061 20190131 MGI PMID:30322915 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0013658 abnormal myeloid cell morphology IAGP N RGD:5509061 20190131 MGI PMID:30322915 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0013659 abnormal erythroid lineage cell morphology IAGP N RGD:5509061 20190131 MGI PMID:30322915 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20190131 MGI PMID:30322915 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0013776 bone marrow failure IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622162 U2af1 U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 1 gene MP:0020464 decreased megakaryocyte progenitor cell number IAGP N RGD:5509061 20211104 MGI PMID:33414485 1622163 Eif4ebp3 eukaryotic translation initiation factor 4E binding protein 3 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20231207 MGI 1622163 Eif4ebp3 eukaryotic translation initiation factor 4E binding protein 3 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 1622164 Smim3 small integral membrane protein 3 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20150409 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0013657 abnormal blood cell morphology IAGP N RGD:5509061 20150409 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20150409 MGI PMID:19966810 1622164 Smim3 small integral membrane protein 3 gene MP:0013705 decreased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20150409 MGI PMID:19966810 1622165 Oard1 O-acyl-ADP-ribose deacylase 1 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20210128 MGI 1622167 Fam170b family with sequence similarity 170, member B gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200924 MGI PMID:32588889 1622167 Fam170b family with sequence similarity 170, member B gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200924 MGI PMID:32588889 1622168 Exoc5 exocyst complex component 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20160616 MGI PMID:26046524 1622168 Exoc5 exocyst complex component 5 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20160616 MGI PMID:26046524 1622168 Exoc5 exocyst complex component 5 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20190718 MGI PMID:27511831 1622168 Exoc5 exocyst complex component 5 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20190718 MGI PMID:27511831 1622168 Exoc5 exocyst complex component 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160616 MGI PMID:26046524 1622168 Exoc5 exocyst complex component 5 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20160616 MGI PMID:26046524 1622168 Exoc5 exocyst complex component 5 gene MP:0003587 ureter obstruction IAGP N RGD:5509061 20160616 MGI PMID:26046524 1622168 Exoc5 exocyst complex component 5 gene MP:0003589 abnormal ureter physiology IAGP N RGD:5509061 20160616 MGI PMID:26046524 1622168 Exoc5 exocyst complex component 5 gene MP:0003589 abnormal ureter physiology IAGP N RGD:5509061 20190718 MGI PMID:27511831 1622168 Exoc5 exocyst complex component 5 gene MP:0003624 anuria IAGP N RGD:5509061 20160616 MGI PMID:26046524 1622168 Exoc5 exocyst complex component 5 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20160616 MGI PMID:26046524 1622168 Exoc5 exocyst complex component 5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160616 MGI PMID:26046524 1622168 Exoc5 exocyst complex component 5 gene MP:0011426 abnormal ureter smooth muscle morphology IAGP N RGD:5509061 20160616 MGI PMID:26046524 1622168 Exoc5 exocyst complex component 5 gene MP:0011484 abnormal ureter urothelium morphology IAGP N RGD:5509061 20160616 MGI PMID:26046524 1622168 Exoc5 exocyst complex component 5 gene MP:0011484 abnormal ureter urothelium morphology IAGP N RGD:5509061 20190718 MGI PMID:27511831 1622168 Exoc5 exocyst complex component 5 gene MP:0011491 ureteropelvic junction obstruction IAGP N RGD:5509061 20160616 MGI PMID:26046524 1622168 Exoc5 exocyst complex component 5 gene MP:0011491 ureteropelvic junction obstruction IAGP N RGD:5509061 20190718 MGI PMID:27511831 1622169 Ezhip EZH inhibitory protein gene MP:0001127 small ovary IAGP N RGD:5509061 20200430 MGI PMID:31451685 1622169 Ezhip EZH inhibitory protein gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200430 MGI PMID:31451685 1622169 Ezhip EZH inhibitory protein gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200430 MGI PMID:31451685 1622169 Ezhip EZH inhibitory protein gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20200430 MGI PMID:31451685 1622169 Ezhip EZH inhibitory protein gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20200430 MGI PMID:31451685 1622169 Ezhip EZH inhibitory protein gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20200430 MGI PMID:31451685 1622176 Spty2d1 SPT2 chromatin protein domain containing 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220811 MGI 1622176 Spty2d1 SPT2 chromatin protein domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622176 Spty2d1 SPT2 chromatin protein domain containing 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220519 MGI 1622177 Pwwp2b PWWP domain containing 2B gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20220224 MGI PMID:34180153 1622177 Pwwp2b PWWP domain containing 2B gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20220224 MGI PMID:34180153 1622177 Pwwp2b PWWP domain containing 2B gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20220224 MGI PMID:34180153 1622177 Pwwp2b PWWP domain containing 2B gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20220224 MGI PMID:34180153 1622177 Pwwp2b PWWP domain containing 2B gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220811 MGI 1622177 Pwwp2b PWWP domain containing 2B gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20220224 MGI PMID:34180153 1622177 Pwwp2b PWWP domain containing 2B gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20220224 MGI PMID:34180153 1622177 Pwwp2b PWWP domain containing 2B gene MP:0009122 decreased white fat cell lipid droplet size IAGP N RGD:5509061 20220224 MGI PMID:34180153 1622177 Pwwp2b PWWP domain containing 2B gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20220224 MGI PMID:34180153 1622177 Pwwp2b PWWP domain containing 2B gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20220224 MGI PMID:34180153 1622177 Pwwp2b PWWP domain containing 2B gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20220224 MGI PMID:34180153 1622177 Pwwp2b PWWP domain containing 2B gene MP:0011019 abnormal adaptive thermogenesis IAGP N RGD:5509061 20220224 MGI PMID:34180153 1622177 Pwwp2b PWWP domain containing 2B gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20220224 MGI PMID:34180153 1622177 Pwwp2b PWWP domain containing 2B gene MP:0020520 whitened brown adipose tissue morphology IAGP N RGD:5509061 20220224 MGI PMID:34180153 1622178 AI467606 expressed sequence AI467606 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1622181 Cers1 ceramide synthase 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1622181 Cers1 ceramide synthase 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15248193 1622181 Cers1 ceramide synthase 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:15248193 1622181 Cers1 ceramide synthase 1 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23074226 1622181 Cers1 ceramide synthase 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15248193 1622181 Cers1 ceramide synthase 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21625621 1622181 Cers1 ceramide synthase 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:23074226 1622181 Cers1 ceramide synthase 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:23074226 1622181 Cers1 ceramide synthase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15248193 1622181 Cers1 ceramide synthase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21625621 1622181 Cers1 ceramide synthase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21625621 1622181 Cers1 ceramide synthase 1 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23074226 1622181 Cers1 ceramide synthase 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15248193 1622181 Cers1 ceramide synthase 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21625621 1622181 Cers1 ceramide synthase 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21625621 1622181 Cers1 ceramide synthase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23074226 1622181 Cers1 ceramide synthase 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:15248193 1622181 Cers1 ceramide synthase 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:21625621 1622181 Cers1 ceramide synthase 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:23074226 1622181 Cers1 ceramide synthase 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15248193 1622181 Cers1 ceramide synthase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15248193 1622181 Cers1 ceramide synthase 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21625621 1622181 Cers1 ceramide synthase 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23074226 1622181 Cers1 ceramide synthase 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:15248193 1622181 Cers1 ceramide synthase 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:15248193 1622181 Cers1 ceramide synthase 1 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:23074226 1622181 Cers1 ceramide synthase 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23074226 1622181 Cers1 ceramide synthase 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:21625621 1622181 Cers1 ceramide synthase 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23074226 1622181 Cers1 ceramide synthase 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:23074226 1622181 Cers1 ceramide synthase 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:23074226 1622181 Cers1 ceramide synthase 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:15248193 1622181 Cers1 ceramide synthase 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:21625621 1622181 Cers1 ceramide synthase 1 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20141003 MGI PMID:21625621 1622181 Cers1 ceramide synthase 1 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20141003 MGI PMID:23074226 1622181 Cers1 ceramide synthase 1 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:23074226 1622181 Cers1 ceramide synthase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1622181 Cers1 ceramide synthase 1 gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:23074226 1622182 Fzd10 frizzled class receptor 10 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1622186 Uchl4 ubiquitin carboxyl-terminal esterase L4 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20210128 MGI 1622186 Uchl4 ubiquitin carboxyl-terminal esterase L4 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1622189 Pramel1 PRAME like 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20190502 MGI 1622189 Pramel1 PRAME like 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1622189 Pramel1 PRAME like 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20190502 MGI 1622189 Pramel1 PRAME like 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20190502 MGI 1622189 Pramel1 PRAME like 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1622189 Pramel1 PRAME like 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20190502 MGI 1622189 Pramel1 PRAME like 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20190502 MGI 1622190 Ngrn neugrin, neurite outgrowth associated gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23677977 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23677977 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23677977 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23677977 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21308854 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23677977 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0004218 meiotic nondisjunction during M1 phase IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21308854 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23677977 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23677977 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:19345203 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0009240 elongated sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:23677977 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23677977 1622191 Nxf2 nuclear RNA export factor 2 gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23677977 1622193 Rsph6a radial spoke head 6 homolog A (Chlamydomonas) gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20181122 MGI PMID:30185526 1622193 Rsph6a radial spoke head 6 homolog A (Chlamydomonas) gene MP:0001925 male infertility IAGP N RGD:5509061 20181122 MGI PMID:30185526 1622193 Rsph6a radial spoke head 6 homolog A (Chlamydomonas) gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20181122 MGI PMID:30185526 1622193 Rsph6a radial spoke head 6 homolog A (Chlamydomonas) gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20181122 MGI PMID:30185526 1622193 Rsph6a radial spoke head 6 homolog A (Chlamydomonas) gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20181122 MGI PMID:30185526 1622193 Rsph6a radial spoke head 6 homolog A (Chlamydomonas) gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20181122 MGI PMID:30185526 1622193 Rsph6a radial spoke head 6 homolog A (Chlamydomonas) gene MP:0020869 immotile sperm IAGP N RGD:5509061 20190912 MGI PMID:30185526 1622193 Rsph6a radial spoke head 6 homolog A (Chlamydomonas) gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20181122 MGI PMID:30185526 1622193 Rsph6a radial spoke head 6 homolog A (Chlamydomonas) gene MP:0031375 abnormal manchette disassembly IAGP N RGD:5509061 20220407 MGI PMID:30185526 1622194 Ucn3 urocortin 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1622194 Ucn3 urocortin 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1622194 Ucn3 urocortin 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:20610744 1622194 Ucn3 urocortin 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17360501 1622194 Ucn3 urocortin 3 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17360501 1622194 Ucn3 urocortin 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17360501 1622194 Ucn3 urocortin 3 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210520 MGI 1622194 Ucn3 urocortin 3 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:17360501 1622195 Gimap3 GTPase, IMAP family member 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20190425 MGI PMID:24510501 1622195 Gimap3 GTPase, IMAP family member 3 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20190502 MGI 1622195 Gimap3 GTPase, IMAP family member 3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20190425 MGI PMID:24510501 1622204 Armcx1 armadillo repeat containing, X-linked 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1622204 Armcx1 armadillo repeat containing, X-linked 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1622204 Armcx1 armadillo repeat containing, X-linked 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1622204 Armcx1 armadillo repeat containing, X-linked 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1622204 Armcx1 armadillo repeat containing, X-linked 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 1622206 Dnajc21 DnaJ heat shock protein family (Hsp40) member C21 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1622206 Dnajc21 DnaJ heat shock protein family (Hsp40) member C21 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20211021 MGI 1622206 Dnajc21 DnaJ heat shock protein family (Hsp40) member C21 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20170105 MGI 1622208 Spink12 serine peptidase inhibitor, Kazal type 12 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1622208 Spink12 serine peptidase inhibitor, Kazal type 12 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20201231 MGI 1622208 Spink12 serine peptidase inhibitor, Kazal type 12 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 1622208 Spink12 serine peptidase inhibitor, Kazal type 12 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1622208 Spink12 serine peptidase inhibitor, Kazal type 12 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 1622208 Spink12 serine peptidase inhibitor, Kazal type 12 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1622208 Spink12 serine peptidase inhibitor, Kazal type 12 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20220811 MGI 1622208 Spink12 serine peptidase inhibitor, Kazal type 12 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210520 MGI 1622217 Sult2a8 sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 8 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20220519 MGI 1622218 Bcas1 brain enriched myelin associated protein 1 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20181227 MGI 1622218 Bcas1 brain enriched myelin associated protein 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20191017 MGI PMID:28230289 1622218 Bcas1 brain enriched myelin associated protein 1 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20191017 MGI PMID:28230289 1622218 Bcas1 brain enriched myelin associated protein 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20191017 MGI PMID:28230289 1622218 Bcas1 brain enriched myelin associated protein 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20191017 MGI PMID:28230289 1622218 Bcas1 brain enriched myelin associated protein 1 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20191017 MGI PMID:28230289 1622218 Bcas1 brain enriched myelin associated protein 1 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20191017 MGI PMID:28230289 1622222 Ifi27l2a interferon, alpha-inducible protein 27 like 2A gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1622222 Ifi27l2a interferon, alpha-inducible protein 27 like 2A gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20181227 MGI 1622222 Ifi27l2a interferon, alpha-inducible protein 27 like 2A gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1622222 Ifi27l2a interferon, alpha-inducible protein 27 like 2A gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1622222 Ifi27l2a interferon, alpha-inducible protein 27 like 2A gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1622222 Ifi27l2a interferon, alpha-inducible protein 27 like 2A gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1622222 Ifi27l2a interferon, alpha-inducible protein 27 like 2A gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1622222 Ifi27l2a interferon, alpha-inducible protein 27 like 2A gene MP:0010897 abnormal bronchiole epithelium morphology IAGP N RGD:5509061 20160310 MGI PMID:25184786 1622222 Ifi27l2a interferon, alpha-inducible protein 27 like 2A gene MP:0011999 abnormal tail length IEA N RGD:5509061 20201022 MGI 1622223 Spata46 spermatogenesis associated 46 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20191010 MGI PMID:27488028 1622223 Spata46 spermatogenesis associated 46 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1622223 Spata46 spermatogenesis associated 46 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1622223 Spata46 spermatogenesis associated 46 gene MP:0000277 abnormal heart shape IEA N RGD:5509061 20210520 MGI 1622223 Spata46 spermatogenesis associated 46 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1622223 Spata46 spermatogenesis associated 46 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210520 MGI 1622223 Spata46 spermatogenesis associated 46 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20191010 MGI PMID:27488028 1622223 Spata46 spermatogenesis associated 46 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20191010 MGI PMID:27488028 1622223 Spata46 spermatogenesis associated 46 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1622223 Spata46 spermatogenesis associated 46 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210520 MGI 1622223 Spata46 spermatogenesis associated 46 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210520 MGI 1622223 Spata46 spermatogenesis associated 46 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20191010 MGI PMID:27488028 1622223 Spata46 spermatogenesis associated 46 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20191010 MGI PMID:27488028 1622223 Spata46 spermatogenesis associated 46 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20191010 MGI PMID:27488028 1622223 Spata46 spermatogenesis associated 46 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20191010 MGI PMID:27488028 1622223 Spata46 spermatogenesis associated 46 gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20210520 MGI 1622223 Spata46 spermatogenesis associated 46 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20191010 MGI PMID:27488028 1622223 Spata46 spermatogenesis associated 46 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 1622223 Spata46 spermatogenesis associated 46 gene MP:0030980 abnormal acroplaxome morphology IAGP N RGD:5509061 20191010 MGI PMID:27488028 1622224 Arrdc5 arrestin domain containing 5 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20210520 MGI 1622224 Arrdc5 arrestin domain containing 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20231109 MGI PMID:37069147 1622224 Arrdc5 arrestin domain containing 5 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20231109 MGI PMID:37069147 1622224 Arrdc5 arrestin domain containing 5 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20231109 MGI PMID:37069147 1622224 Arrdc5 arrestin domain containing 5 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20231109 MGI PMID:37069147 1622224 Arrdc5 arrestin domain containing 5 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1622224 Arrdc5 arrestin domain containing 5 gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20231109 MGI PMID:37069147 1622224 Arrdc5 arrestin domain containing 5 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20231109 MGI PMID:37069147 1622224 Arrdc5 arrestin domain containing 5 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 1622224 Arrdc5 arrestin domain containing 5 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20231109 MGI PMID:37069147 1622224 Arrdc5 arrestin domain containing 5 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20231109 MGI PMID:37069147 1622224 Arrdc5 arrestin domain containing 5 gene MP:0009233 enlarged sperm head IAGP N RGD:5509061 20231109 MGI PMID:37069147 1622224 Arrdc5 arrestin domain containing 5 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20181227 MGI 1622224 Arrdc5 arrestin domain containing 5 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20231109 MGI PMID:37069147 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20170504 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20141003 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0000601 small liver IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0000644 dextrocardia IEA N RGD:5509061 20141003 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20170504 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0002747 abnormal aortic valve morphology IEA N RGD:5509061 20170504 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0002766 situs inversus IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0002767 situs ambiguus IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20170504 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0003943 abnormal hepatobiliary system development IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0004110 transposition of great arteries IEA N RGD:5509061 20170504 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0004201 fetal growth retardation IEA N RGD:5509061 20170504 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0006061 right atrial isomerism IEA N RGD:5509061 20141003 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20141003 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0008992 abnormal portal lobule morphology IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141003 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0010406 common atrium IEA N RGD:5509061 20170504 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20141003 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0010440 anomalous pulmonary venous connection IEA N RGD:5509061 20170504 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0010607 common atrioventricular valve IEA N RGD:5509061 20170504 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0010854 lung situs inversus IEA N RGD:5509061 20170504 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0011249 abdominal situs inversus IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20141003 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0012238 abnormal cholangiocyte primary cilium morphology IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0013611 abnormal bile duct epithelium morphology IAGP N RGD:5509061 20210812 MGI PMID:32886109 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0013975 abnormal coronary sinus connection IEA N RGD:5509061 20170504 MGI 1622226 Anks6 ankyrin repeat and sterile alpha motif domain containing 6 gene MP:0013977 symmetric azygos veins IEA N RGD:5509061 20170504 MGI 1622229 Tex22 testis expressed gene 22 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:27357688 1622230 Tmem225 transmembrane protein 225 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1622230 Tmem225 transmembrane protein 225 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1622230 Tmem225 transmembrane protein 225 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 1622230 Tmem225 transmembrane protein 225 gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1622230 Tmem225 transmembrane protein 225 gene MP:0001925 male infertility IAGP N RGD:5509061 20241107 MGI PMID:38246484 1622230 Tmem225 transmembrane protein 225 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20241107 MGI PMID:38246484 1622230 Tmem225 transmembrane protein 225 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1622230 Tmem225 transmembrane protein 225 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20241107 MGI PMID:38246484 1622230 Tmem225 transmembrane protein 225 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1622230 Tmem225 transmembrane protein 225 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20241107 MGI PMID:38246484 1622230 Tmem225 transmembrane protein 225 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20241107 MGI PMID:38246484 1622230 Tmem225 transmembrane protein 225 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20241107 MGI PMID:38246484 1622230 Tmem225 transmembrane protein 225 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20241107 MGI PMID:38246484 1622230 Tmem225 transmembrane protein 225 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1622230 Tmem225 transmembrane protein 225 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20241107 MGI PMID:38246484 1622230 Tmem225 transmembrane protein 225 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20241107 MGI PMID:38246484 1622230 Tmem225 transmembrane protein 225 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20241107 MGI PMID:38246484 1622230 Tmem225 transmembrane protein 225 gene MP:0014246 decreased cellular ATP level IAGP N RGD:5509061 20241107 MGI PMID:38246484 1622230 Tmem225 transmembrane protein 225 gene MP:0014537 increased calcium level IAGP N RGD:5509061 20241107 MGI PMID:38246484 1622230 Tmem225 transmembrane protein 225 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20211021 MGI 1622230 Tmem225 transmembrane protein 225 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20241107 MGI PMID:38246484 1622232 1700020A23Rik RIKEN cDNA 1700020A23 gene gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1622234 Ssmem1 serine-rich single-pass membrane protein 1 gene MP:0001147 small testis IAGP N RGD:5509061 20210422 MGI PMID:32301969 1622234 Ssmem1 serine-rich single-pass membrane protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20210422 MGI PMID:32301969 1622234 Ssmem1 serine-rich single-pass membrane protein 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20210422 MGI PMID:32301969 1622234 Ssmem1 serine-rich single-pass membrane protein 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210422 MGI PMID:32301969 1622234 Ssmem1 serine-rich single-pass membrane protein 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20210422 MGI PMID:32301969 1622234 Ssmem1 serine-rich single-pass membrane protein 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210422 MGI PMID:32301969 1622234 Ssmem1 serine-rich single-pass membrane protein 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210422 MGI PMID:32301969 1622236 Spata25 spermatogenesis associated 25 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1622237 Frey1 Frey regulator of sperm-oocyte fusion 1 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20231207 MGI 1622237 Frey1 Frey regulator of sperm-oocyte fusion 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20230727 MGI PMID:36787362 1622237 Frey1 Frey regulator of sperm-oocyte fusion 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20230727 MGI PMID:36787362 1622237 Frey1 Frey regulator of sperm-oocyte fusion 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20221201 MGI PMID:35960805 1622237 Frey1 Frey regulator of sperm-oocyte fusion 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20230727 MGI PMID:36787362 1622237 Frey1 Frey regulator of sperm-oocyte fusion 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230720 MGI 1622237 Frey1 Frey regulator of sperm-oocyte fusion 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20230727 MGI PMID:36787362 1622237 Frey1 Frey regulator of sperm-oocyte fusion 1 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20230727 MGI PMID:36787362 1622237 Frey1 Frey regulator of sperm-oocyte fusion 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20231207 MGI 1622237 Frey1 Frey regulator of sperm-oocyte fusion 1 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20221201 MGI PMID:35960805 1622237 Frey1 Frey regulator of sperm-oocyte fusion 1 gene MP:0031010 failure of sperm-egg fusion IAGP N RGD:5509061 20221201 MGI PMID:35960805 1622237 Frey1 Frey regulator of sperm-oocyte fusion 1 gene MP:0031010 failure of sperm-egg fusion IAGP N RGD:5509061 20230727 MGI PMID:36787362 1622240 Kxd1 KxDL motif containing 1 gene MP:0010192 abnormal retina melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:22554196 1622240 Kxd1 KxDL motif containing 1 gene MP:0010193 abnormal choroid melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:22554196 1622240 Kxd1 KxDL motif containing 1 gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170720 MGI PMID:22554196 1622243 Wnk2 WNK lysine deficient protein kinase 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1622243 Wnk2 WNK lysine deficient protein kinase 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20201022 MGI 1622244 Smlr1 small leucine-rich protein 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20241031 MGI PMID:36053190 1622246 Duxf3 double homeobox family member 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20231026 MGI PMID:31591446 1622247 Epcip exosomal polycystin 1 interacting protein gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20240523 MGI 1622248 Ubap2l ubiquitin-associated protein 2-like gene MP:0001265 decreased body size IEA N RGD:5509061 20200310 MGI 1622248 Ubap2l ubiquitin-associated protein 2-like gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1622248 Ubap2l ubiquitin-associated protein 2-like gene MP:0001923 reduced female fertility IEA N RGD:5509061 20200310 MGI 1622248 Ubap2l ubiquitin-associated protein 2-like gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 1622248 Ubap2l ubiquitin-associated protein 2-like gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20221215 MGI 1622248 Ubap2l ubiquitin-associated protein 2-like gene MP:0005333 decreased heart rate IEA N RGD:5509061 20231207 MGI 1622248 Ubap2l ubiquitin-associated protein 2-like gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210128 MGI 1622248 Ubap2l ubiquitin-associated protein 2-like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622249 Spag17 sperm associated antigen 17 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0001177 atelectasis IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1622249 Spag17 sperm associated antigen 17 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0001513 limb grasping IEA N RGD:5509061 20201231 MGI 1622249 Spag17 sperm associated antigen 17 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1622249 Spag17 sperm associated antigen 17 gene MP:0001575 cyanosis IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0001925 male infertility IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0009242 thin sperm flagellum IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0010898 abnormal pulmonary alveolus epithelium morphology IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0011649 immotile respiratory cilia IAGP N RGD:5509061 20160218 MGI PMID:23418344 1622249 Spag17 sperm associated antigen 17 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0030591 absent sperm fibrous sheath IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0031374 abnormal manchette assembly IAGP N RGD:5509061 20220407 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20220428 MGI PMID:29690537 1622249 Spag17 sperm associated antigen 17 gene MP:0031387 abnormal intramanchette transport IAGP N RGD:5509061 20220428 MGI PMID:29690537 1622250 4931429L15Rik RIKEN cDNA 4931429L15 gene gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210128 MGI 1622250 4931429L15Rik RIKEN cDNA 4931429L15 gene gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 1622251 4931414P19Rik RIKEN cDNA 4931414P19 gene gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20191003 MGI PMID:28230092 1622251 4931414P19Rik RIKEN cDNA 4931414P19 gene gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20191003 MGI PMID:28230092 1622251 4931414P19Rik RIKEN cDNA 4931414P19 gene gene MP:0005471 decreased thyroxine level IAGP N RGD:5509061 20191003 MGI PMID:28230092 1622251 4931414P19Rik RIKEN cDNA 4931414P19 gene gene MP:0005473 decreased triiodothyronine level IAGP N RGD:5509061 20191003 MGI PMID:28230092 1622252 Matcap1 microtubule associated tyrosine carboxypeptidase 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20220707 MGI PMID:35482892 1622252 Matcap1 microtubule associated tyrosine carboxypeptidase 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20220707 MGI PMID:35482892 1622252 Matcap1 microtubule associated tyrosine carboxypeptidase 1 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20220707 MGI PMID:35482892 1622252 Matcap1 microtubule associated tyrosine carboxypeptidase 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20220707 MGI PMID:35482892 1622252 Matcap1 microtubule associated tyrosine carboxypeptidase 1 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20220707 MGI PMID:35482892 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20230601 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230601 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20230601 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20230601 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0001258 decreased body length IEA N RGD:5509061 20240523 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20230601 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20230601 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230601 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20230601 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20230601 MGI 1622253 Fhip1b FHF complex subunit HOOK interacting protein 1B gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20240523 MGI 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:21818371 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21818371 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:21818371 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20180726 MGI PMID:29784826 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19285470 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:21818371 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:21818371 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:21818371 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20180726 MGI PMID:29784826 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:21818371 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:21818371 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:21818371 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:21818371 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:21818371 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21818371 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0009455 enhanced cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21818371 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:21818371 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20180726 MGI PMID:29784826 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20180726 MGI PMID:29784826 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0020510 increased dendritic spine length IAGP N RGD:5509061 20211014 MGI PMID:21818371 1622254 Lrrtm1 leucine rich repeat transmembrane neuronal 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21636576 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21636576 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21636576 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20170126 MGI 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0001764 abnormal homeostasis IEA N RGD:5509061 20170126 MGI 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20170126 MGI 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21636576 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:21636576 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:21636576 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21636576 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0009643 abnormal urine homeostasis IEA N RGD:5509061 20170126 MGI 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21636576 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:21636576 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0011417 abnormal renal transport IAGP N RGD:5509061 20141003 MGI PMID:21636576 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0020406 hyperthreoninuria IAGP N RGD:5509061 20161208 MGI PMID:21636576 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0030616 hyperglycinuria IAGP N RGD:5509061 20240801 MGI PMID:21636576 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0030617 hyperglutaminuria IAGP N RGD:5509061 20240801 MGI PMID:21636576 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0031637 methioninuria IAGP N RGD:5509061 20240801 MGI PMID:21636576 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0031641 alaninuria IAGP N RGD:5509061 20240801 MGI PMID:21636576 1622255 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19 gene MP:0031642 phenylalaninuria IAGP N RGD:5509061 20240801 MGI PMID:21636576 1622256 Palm3 paralemmin 3 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 1622256 Palm3 paralemmin 3 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20190502 MGI 1622256 Palm3 paralemmin 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20190502 MGI 1622259 Sgip1 SH3-domain GRB2-like (endophilin) interacting protein 1 gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20160421 MGI 1622259 Sgip1 SH3-domain GRB2-like (endophilin) interacting protein 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1622259 Sgip1 SH3-domain GRB2-like (endophilin) interacting protein 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20170105 MGI 1622259 Sgip1 SH3-domain GRB2-like (endophilin) interacting protein 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1622259 Sgip1 SH3-domain GRB2-like (endophilin) interacting protein 1 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20181227 MGI 1622259 Sgip1 SH3-domain GRB2-like (endophilin) interacting protein 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1622259 Sgip1 SH3-domain GRB2-like (endophilin) interacting protein 1 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 1622261 2900092C05Rik RIKEN cDNA 2900092C05 gene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1622262 Ppil6 peptidylprolyl isomerase (cyclophilin)-like 6 gene MP:0000745 tremors IEA N RGD:5509061 20240523 MGI 1622262 Ppil6 peptidylprolyl isomerase (cyclophilin)-like 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1622262 Ppil6 peptidylprolyl isomerase (cyclophilin)-like 6 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20240523 MGI 1622269 Trnau1ap tRNA selenocysteine 1 associated protein 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170314 MGI PMID:26043259 1622269 Trnau1ap tRNA selenocysteine 1 associated protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170314 MGI PMID:26043259 1622269 Trnau1ap tRNA selenocysteine 1 associated protein 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20170314 MGI PMID:26043259 1622270 Ankle2 ankyrin repeat and LEM domain containing 2 gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20220519 MGI 1622270 Ankle2 ankyrin repeat and LEM domain containing 2 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1622270 Ankle2 ankyrin repeat and LEM domain containing 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201022 MGI 1622270 Ankle2 ankyrin repeat and LEM domain containing 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0001260 increased body weight IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0001261 obese IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0001433 polyphagia IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0001762 polyuria IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0002959 increased urine microalbumin level IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0005610 increased circulating antidiuretic hormone level IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210520 MGI 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0008138 absent podocyte foot process IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0011431 increased urine flow rate IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0011859 decreased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622272 Bbs10 Bardet-Biedl syndrome 10 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20160929 MGI PMID:26273430 1622273 Raver1 ribonucleoprotein, PTB-binding 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18061163 1622273 Raver1 ribonucleoprotein, PTB-binding 1 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:18061163 1622273 Raver1 ribonucleoprotein, PTB-binding 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20240523 MGI 1622273 Raver1 ribonucleoprotein, PTB-binding 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230601 MGI 1622273 Raver1 ribonucleoprotein, PTB-binding 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20230601 MGI 1622275 Etnppl ethanolamine phosphate phospholyase gene MP:0000745 tremors IEA N RGD:5509061 20240523 MGI 1622275 Etnppl ethanolamine phosphate phospholyase gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20240523 MGI 1622275 Etnppl ethanolamine phosphate phospholyase gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240523 MGI 1622275 Etnppl ethanolamine phosphate phospholyase gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20210923 MGI PMID:34048714 1622278 Map3k13 mitogen-activated protein kinase kinase kinase 13 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:27511108 1622278 Map3k13 mitogen-activated protein kinase kinase kinase 13 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20211028 MGI PMID:27511108 1622278 Map3k13 mitogen-activated protein kinase kinase kinase 13 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20211028 MGI PMID:27511108 1622281 Dhx34 DExH-box helicase 34 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 1622282 Cdc40 cell division cycle 40 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20210325 MGI PMID:33220177 1622282 Cdc40 cell division cycle 40 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1622283 Dram1 DNA-damage regulated autophagy modulator 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1622283 Dram1 DNA-damage regulated autophagy modulator 1 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20210128 MGI 1622283 Dram1 DNA-damage regulated autophagy modulator 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1622284 5730403I07Rik RIKEN cDNA 5730403I07 gene gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20240530 MGI PMID:36038289 1622284 5730403I07Rik RIKEN cDNA 5730403I07 gene gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20240530 MGI PMID:36038289 1622284 5730403I07Rik RIKEN cDNA 5730403I07 gene gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20240530 MGI PMID:36038289 1622284 5730403I07Rik RIKEN cDNA 5730403I07 gene gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20240530 MGI PMID:36038289 1622284 5730403I07Rik RIKEN cDNA 5730403I07 gene gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20240530 MGI PMID:36038289 1622284 5730403I07Rik RIKEN cDNA 5730403I07 gene gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20240530 MGI PMID:36038289 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0009127 increased brown fat cell number IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210805 MGI 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:21164481 1622286 Crtc3 CREB regulated transcription coactivator 3 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:21164481 1622287 Mpc2 mitochondrial pyruvate carrier 2 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20181101 MGI PMID:24910426 1622287 Mpc2 mitochondrial pyruvate carrier 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20181101 MGI PMID:24910426 1622287 Mpc2 mitochondrial pyruvate carrier 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20181101 MGI PMID:24910426 1622287 Mpc2 mitochondrial pyruvate carrier 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20181101 MGI PMID:24910426 1622287 Mpc2 mitochondrial pyruvate carrier 2 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20181101 MGI PMID:24910426 1622287 Mpc2 mitochondrial pyruvate carrier 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20181101 MGI PMID:24910426 1622287 Mpc2 mitochondrial pyruvate carrier 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20181101 MGI PMID:24910426 1622287 Mpc2 mitochondrial pyruvate carrier 2 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20181101 MGI PMID:24910426 1622287 Mpc2 mitochondrial pyruvate carrier 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20181101 MGI PMID:24910426 1622287 Mpc2 mitochondrial pyruvate carrier 2 gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20181101 MGI PMID:24910426 1622288 Draxin dorsal inhibitory axon guidance protein gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:19150847 1622288 Draxin dorsal inhibitory axon guidance protein gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:19150847 1622288 Draxin dorsal inhibitory axon guidance protein gene MP:0002727 decreased circulating insulin level IEA N RGD:5509061 20170323 MGI 1622288 Draxin dorsal inhibitory axon guidance protein gene MP:0004100 abnormal spinal cord interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19150847 1622288 Draxin dorsal inhibitory axon guidance protein gene MP:0008222 decreased hippocampal commissure size IAGP N RGD:5509061 20141003 MGI PMID:19150847 1622288 Draxin dorsal inhibitory axon guidance protein gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:19150847 1622288 Draxin dorsal inhibitory axon guidance protein gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:19150847 1622288 Draxin dorsal inhibitory axon guidance protein gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:19150847 1622289 Tspan15 tetraspanin 15 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1622289 Tspan15 tetraspanin 15 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20230601 MGI 1622289 Tspan15 tetraspanin 15 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20240307 MGI PMID:29520422 1622289 Tspan15 tetraspanin 15 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1622292 Dym dymeclin gene MP:0000120 malocclusion IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20200514 MGI 1622292 Dym dymeclin gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0001488 increased startle reflex IEA N RGD:5509061 20201022 MGI 1622292 Dym dymeclin gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1622292 Dym dymeclin gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1622292 Dym dymeclin gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20200514 MGI 1622292 Dym dymeclin gene MP:0002764 short tibia IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20201231 MGI 1622292 Dym dymeclin gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20200514 MGI 1622292 Dym dymeclin gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200514 MGI 1622292 Dym dymeclin gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0003109 short femur IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0003587 ureter obstruction IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20200514 MGI 1622292 Dym dymeclin gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0004351 short humerus IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0004610 small vertebrae IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0004672 short ribs IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200514 MGI 1622292 Dym dymeclin gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20200514 MGI 1622292 Dym dymeclin gene MP:0005352 small cranium IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0008526 decreased cranium width IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1622292 Dym dymeclin gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1622292 Dym dymeclin gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200514 MGI 1622292 Dym dymeclin gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20200310 MGI PMID:18852472 1622292 Dym dymeclin gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1622292 Dym dymeclin gene MP:0014239 abnormal intracellular organelle morphology IAGP N RGD:5509061 20230615 MGI PMID:18852472 1622293 Mcemp1 mast cell expressed membrane protein 1 gene MP:0002531 abnormal type I hypersensitivity reaction IAGP N RGD:5509061 20231109 MGI PMID:37041174 1622293 Mcemp1 mast cell expressed membrane protein 1 gene MP:0005462 abnormal mast cell differentiation IAGP N RGD:5509061 20231109 MGI PMID:37041174 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18854576 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18818388 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220203 MGI PMID:22069496 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220203 MGI PMID:22069496 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18854576 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18818388 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18854576 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0001925 male infertility IAGP N RGD:5509061 20220203 MGI PMID:22069496 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220203 MGI PMID:22069496 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18818388 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18854576 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18854576 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0002415 abnormal neutrophil differentiation IAGP N RGD:5509061 20141003 MGI PMID:18854576 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:18854576 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18854576 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220203 MGI PMID:22069496 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220203 MGI PMID:22069496 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:18854576 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18818388 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18818388 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18818388 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:18854576 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:18818388 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:18818388 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:18854576 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0008850 increased hemoglobin concentration distribution width IAGP N RGD:5509061 20141003 MGI PMID:18854576 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220203 MGI PMID:22069496 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220203 MGI PMID:22069496 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0009231 detached acrosome IAGP N RGD:5509061 20220203 MGI PMID:22069496 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220203 MGI PMID:22069496 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18854576 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18818388 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18818388 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18952892 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18854576 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0013320 dilated seminal vesicle IAGP N RGD:5509061 20141204 MGI PMID:18854576 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220203 MGI PMID:22069496 1622294 Kmt2e lysine (K)-specific methyltransferase 2E gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20220203 MGI PMID:22069496 1622295 Tmem256 transmembrane protein 256 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20231207 MGI 1622295 Tmem256 transmembrane protein 256 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20231207 MGI 1622295 Tmem256 transmembrane protein 256 gene MP:0001513 limb grasping IEA N RGD:5509061 20210520 MGI 1622295 Tmem256 transmembrane protein 256 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20210520 MGI 1622295 Tmem256 transmembrane protein 256 gene MP:0002764 short tibia IEA N RGD:5509061 20160114 MGI 1622295 Tmem256 transmembrane protein 256 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20231207 MGI 1622295 Tmem256 transmembrane protein 256 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 1622295 Tmem256 transmembrane protein 256 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 1622295 Tmem256 transmembrane protein 256 gene MP:0010511 shortened PR interval IEA N RGD:5509061 20220811 MGI 1622295 Tmem256 transmembrane protein 256 gene MP:0010571 shortened ST segment IEA N RGD:5509061 20210128 MGI 1622296 Dyrk2 dual-specificity tyrosine phosphorylation regulated kinase 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20210603 MGI PMID:32758357 1622296 Dyrk2 dual-specificity tyrosine phosphorylation regulated kinase 2 gene MP:0000445 short snout IAGP N RGD:5509061 20210603 MGI PMID:32758357 1622296 Dyrk2 dual-specificity tyrosine phosphorylation regulated kinase 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20210603 MGI PMID:32758357 1622296 Dyrk2 dual-specificity tyrosine phosphorylation regulated kinase 2 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20210603 MGI PMID:32758357 1622296 Dyrk2 dual-specificity tyrosine phosphorylation regulated kinase 2 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20210603 MGI PMID:32758357 1622296 Dyrk2 dual-specificity tyrosine phosphorylation regulated kinase 2 gene MP:0008385 absent basisphenoid bone IAGP N RGD:5509061 20210603 MGI PMID:32758357 1622296 Dyrk2 dual-specificity tyrosine phosphorylation regulated kinase 2 gene MP:0009609 absent basioccipital bone IAGP N RGD:5509061 20210603 MGI PMID:32758357 1622296 Dyrk2 dual-specificity tyrosine phosphorylation regulated kinase 2 gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20210603 MGI PMID:32758357 1622296 Dyrk2 dual-specificity tyrosine phosphorylation regulated kinase 2 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20210603 MGI PMID:32758357 1622296 Dyrk2 dual-specificity tyrosine phosphorylation regulated kinase 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20210603 MGI PMID:32758357 1622296 Dyrk2 dual-specificity tyrosine phosphorylation regulated kinase 2 gene MP:0012361 decreased large unstained cell number IEA N RGD:5509061 20210128 MGI 1622296 Dyrk2 dual-specificity tyrosine phosphorylation regulated kinase 2 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20210603 MGI PMID:32758357 1622296 Dyrk2 dual-specificity tyrosine phosphorylation regulated kinase 2 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20210603 MGI PMID:32758357 1622297 Stimate STIM activating enhancer gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1622297 Stimate STIM activating enhancer gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1622298 Chaserr CHD2 adjacent suppressive regulatory RNA gene MP:0000120 malocclusion IAGP N RGD:5509061 20200123 MGI PMID:31704914 1622298 Chaserr CHD2 adjacent suppressive regulatory RNA gene MP:0000160 kyphosis IAGP N RGD:5509061 20200123 MGI PMID:31704914 1622298 Chaserr CHD2 adjacent suppressive regulatory RNA gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200123 MGI PMID:31704914 1622298 Chaserr CHD2 adjacent suppressive regulatory RNA gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200123 MGI PMID:31704914 1622298 Chaserr CHD2 adjacent suppressive regulatory RNA gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200123 MGI PMID:31704914 1622298 Chaserr CHD2 adjacent suppressive regulatory RNA gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20200123 MGI PMID:31704914 1622298 Chaserr CHD2 adjacent suppressive regulatory RNA gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20200123 MGI PMID:31704914 1622298 Chaserr CHD2 adjacent suppressive regulatory RNA gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200123 MGI PMID:31704914 1622298 Chaserr CHD2 adjacent suppressive regulatory RNA gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200123 MGI PMID:31704914 1622298 Chaserr CHD2 adjacent suppressive regulatory RNA gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200123 MGI PMID:31704914 1622299 Fcmr Fc fragment of IgM receptor gene MP:0000642 enlarged adrenal glands IEA N RGD:5509061 20160811 MGI 1622299 Fcmr Fc fragment of IgM receptor gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22984178 1622299 Fcmr Fc fragment of IgM receptor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23359703 1622299 Fcmr Fc fragment of IgM receptor gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23359703 1622299 Fcmr Fc fragment of IgM receptor gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:22984178 1622299 Fcmr Fc fragment of IgM receptor gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22984178 1622299 Fcmr Fc fragment of IgM receptor gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21613257 1622299 Fcmr Fc fragment of IgM receptor gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:23359703 1622299 Fcmr Fc fragment of IgM receptor gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:22984178 1622299 Fcmr Fc fragment of IgM receptor gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:22984178 1622299 Fcmr Fc fragment of IgM receptor gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22984178 1622299 Fcmr Fc fragment of IgM receptor gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22984178 1622299 Fcmr Fc fragment of IgM receptor gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22984178 1622299 Fcmr Fc fragment of IgM receptor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21613257 1622299 Fcmr Fc fragment of IgM receptor gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:22984178 1622299 Fcmr Fc fragment of IgM receptor gene MP:0005074 impaired granulocyte bactericidal activity IAGP N RGD:5509061 20141003 MGI PMID:23359703 1622299 Fcmr Fc fragment of IgM receptor gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:21613257 1622299 Fcmr Fc fragment of IgM receptor gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21613257 1622299 Fcmr Fc fragment of IgM receptor gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:22984178 1622299 Fcmr Fc fragment of IgM receptor gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22984178 1622299 Fcmr Fc fragment of IgM receptor gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:22984178 1622299 Fcmr Fc fragment of IgM receptor gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23359703 1622299 Fcmr Fc fragment of IgM receptor gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:23359703 1622299 Fcmr Fc fragment of IgM receptor gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1622299 Fcmr Fc fragment of IgM receptor gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21613257 1622299 Fcmr Fc fragment of IgM receptor gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23359703 1622299 Fcmr Fc fragment of IgM receptor gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23359703 1622302 Tusc1 tumor suppressor candidate 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1622305 Coa6 cytochrome c oxidase assembly factor 6 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20200514 MGI 1622305 Coa6 cytochrome c oxidase assembly factor 6 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1622305 Coa6 cytochrome c oxidase assembly factor 6 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 1622305 Coa6 cytochrome c oxidase assembly factor 6 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20201231 MGI 1622305 Coa6 cytochrome c oxidase assembly factor 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1622305 Coa6 cytochrome c oxidase assembly factor 6 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 1622306 Tmem100 transmembrane protein 100 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 1622306 Tmem100 transmembrane protein 100 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1622306 Tmem100 transmembrane protein 100 gene MP:0000262 poor arterial differentiation IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20201231 MGI 1622306 Tmem100 transmembrane protein 100 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20160811 MGI 1622306 Tmem100 transmembrane protein 100 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1622306 Tmem100 transmembrane protein 100 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1622306 Tmem100 transmembrane protein 100 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 1622306 Tmem100 transmembrane protein 100 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20848592 1622306 Tmem100 transmembrane protein 100 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 1622306 Tmem100 transmembrane protein 100 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0010545 abnormal heart layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20848592 1622306 Tmem100 transmembrane protein 100 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22783020 1622306 Tmem100 transmembrane protein 100 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160811 MGI 1622307 Camsap2 calmodulin regulated spectrin-associated protein family, member 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20210729 MGI PMID:30190432 1622307 Camsap2 calmodulin regulated spectrin-associated protein family, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210729 MGI PMID:30190432 1622307 Camsap2 calmodulin regulated spectrin-associated protein family, member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210729 MGI PMID:30190432 1622307 Camsap2 calmodulin regulated spectrin-associated protein family, member 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20210729 MGI PMID:30190432 1622307 Camsap2 calmodulin regulated spectrin-associated protein family, member 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20210729 MGI PMID:30190432 1622307 Camsap2 calmodulin regulated spectrin-associated protein family, member 2 gene MP:0020581 abnormal neuron polarity IAGP N RGD:5509061 20210729 MGI PMID:30190432 1622313 Cdca5 cell division cycle associated 5 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20210128 MGI 1622313 Cdca5 cell division cycle associated 5 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1622313 Cdca5 cell division cycle associated 5 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20160421 MGI 1622313 Cdca5 cell division cycle associated 5 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1622313 Cdca5 cell division cycle associated 5 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160421 MGI 1622313 Cdca5 cell division cycle associated 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622313 Cdca5 cell division cycle associated 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1622313 Cdca5 cell division cycle associated 5 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1622315 Lce1f late cornified envelope 1F gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1622315 Lce1f late cornified envelope 1F gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1622315 Lce1f late cornified envelope 1F gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20201022 MGI 1622317 Pllp plasma membrane proteolipid gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 1622317 Pllp plasma membrane proteolipid gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 1622317 Pllp plasma membrane proteolipid gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1622317 Pllp plasma membrane proteolipid gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1622317 Pllp plasma membrane proteolipid gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 1622317 Pllp plasma membrane proteolipid gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 1622317 Pllp plasma membrane proteolipid gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1622317 Pllp plasma membrane proteolipid gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20231207 MGI 1622317 Pllp plasma membrane proteolipid gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 1622317 Pllp plasma membrane proteolipid gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 1622319 Exosc1 exosome component 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20220519 MGI 1622319 Exosc1 exosome component 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622319 Exosc1 exosome component 1 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622319 Exosc1 exosome component 1 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622319 Exosc1 exosome component 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622319 Exosc1 exosome component 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622319 Exosc1 exosome component 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622319 Exosc1 exosome component 1 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622319 Exosc1 exosome component 1 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622319 Exosc1 exosome component 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622319 Exosc1 exosome component 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20231207 MGI 1622319 Exosc1 exosome component 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1622319 Exosc1 exosome component 1 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IEA N RGD:5509061 20241017 MGI 1622319 Exosc1 exosome component 1 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622319 Exosc1 exosome component 1 gene MP:0011191 increased embryonic epiblast cell apoptosis IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622319 Exosc1 exosome component 1 gene MP:0011207 absent ectoplacental cavity IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622319 Exosc1 exosome component 1 gene MP:0011209 absent extraembryonic coelom IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622319 Exosc1 exosome component 1 gene MP:0012028 abnormal visceral endoderm physiology IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622319 Exosc1 exosome component 1 gene MP:0012142 absent amniotic cavity IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622319 Exosc1 exosome component 1 gene MP:0014134 abnormal embryo morphology IEA N RGD:5509061 20241017 MGI 1622319 Exosc1 exosome component 1 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20240104 MGI PMID:37940010 1622320 Mis18a MIS18 kinetochore protein A gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:22516971 1622320 Mis18a MIS18 kinetochore protein A gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:22516971 1622320 Mis18a MIS18 kinetochore protein A gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:22516971 1622320 Mis18a MIS18 kinetochore protein A gene MP:0009850 embryonic lethality between implantation and placentation IAGP N RGD:5509061 20141003 MGI PMID:22516971 1622320 Mis18a MIS18 kinetochore protein A gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22516971 1622320 Mis18a MIS18 kinetochore protein A gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:22516971 1622320 Mis18a MIS18 kinetochore protein A gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:22516971 1622321 Rwdd3 RWD domain containing 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20200310 MGI 1622321 Rwdd3 RWD domain containing 3 gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20211021 MGI 1622321 Rwdd3 RWD domain containing 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622323 Rps19bp1 ribosomal protein S19 binding protein 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1622323 Rps19bp1 ribosomal protein S19 binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622323 Rps19bp1 ribosomal protein S19 binding protein 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1622323 Rps19bp1 ribosomal protein S19 binding protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1622324 Rep15 RAB15 effector protein gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20201022 MGI 1622324 Rep15 RAB15 effector protein gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1622324 Rep15 RAB15 effector protein gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 1622328 Timm50 translocase of inner mitochondrial membrane 50 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20211021 MGI 1622328 Timm50 translocase of inner mitochondrial membrane 50 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1622328 Timm50 translocase of inner mitochondrial membrane 50 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1622328 Timm50 translocase of inner mitochondrial membrane 50 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20201231 MGI 1622328 Timm50 translocase of inner mitochondrial membrane 50 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1622328 Timm50 translocase of inner mitochondrial membrane 50 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20191114 MGI PMID:28432072 1622328 Timm50 translocase of inner mitochondrial membrane 50 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1622328 Timm50 translocase of inner mitochondrial membrane 50 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20201022 MGI 1622328 Timm50 translocase of inner mitochondrial membrane 50 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622328 Timm50 translocase of inner mitochondrial membrane 50 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 1622328 Timm50 translocase of inner mitochondrial membrane 50 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1622330 Rwdd1 RWD domain containing 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1622330 Rwdd1 RWD domain containing 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 1622330 Rwdd1 RWD domain containing 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 1622330 Rwdd1 RWD domain containing 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20181227 MGI 1622330 Rwdd1 RWD domain containing 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20181227 MGI 1622330 Rwdd1 RWD domain containing 1 gene MP:0004974 decreased regulatory T cell number IEA N RGD:5509061 20201022 MGI 1622330 Rwdd1 RWD domain containing 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1622330 Rwdd1 RWD domain containing 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1622330 Rwdd1 RWD domain containing 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 1622330 Rwdd1 RWD domain containing 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1622330 Rwdd1 RWD domain containing 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 1622330 Rwdd1 RWD domain containing 1 gene MP:0013418 increased memory-marker gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 1622330 Rwdd1 RWD domain containing 1 gene MP:0013675 decreased Ly6C-positive mature NK cell number IEA N RGD:5509061 20201231 MGI 1622331 Cul7 cullin 7 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20141003 MGI 1622331 Cul7 cullin 7 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:12904573 1622331 Cul7 cullin 7 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1622331 Cul7 cullin 7 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12904573 1622331 Cul7 cullin 7 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:12904573 1622331 Cul7 cullin 7 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:12904573 1622331 Cul7 cullin 7 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12904573 1622331 Cul7 cullin 7 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12904573 1622331 Cul7 cullin 7 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1622331 Cul7 cullin 7 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18498745 1622331 Cul7 cullin 7 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:18498745 1622331 Cul7 cullin 7 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12904573 1622331 Cul7 cullin 7 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18498745 1622332 Chtop chromatin target of PRMT1 gene MP:0000138 absent vertebrae IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0000141 abnormal vertebral body morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0000153 rib bifurcation IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0000154 rib fusion IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0000161 scoliosis IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20190912 MGI PMID:29539633 1622332 Chtop chromatin target of PRMT1 gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0000492 abnormal rectum morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0000497 abnormal small intestine placement IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0000613 abnormal salivary gland morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0000632 abnormal pineal gland morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0000690 absent spleen IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0000820 abnormal choroid plexus morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0000963 fused dorsal root ganglion IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0001088 small nodose ganglion IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0001634 internal hemorrhage IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1622332 Chtop chromatin target of PRMT1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0002745 abnormal atrioventricular valve morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20201231 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0003130 anal atresia IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0003345 decreased rib number IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0003451 absent olfactory bulb IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0003499 thyroid gland hypoplasia IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0003617 urinary bladder hypoplasia IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0003924 diaphragmatic hernia IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0004158 right aortic arch IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0004160 retroesophageal right subclavian artery IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0004163 abnormal adenohypophysis morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0004164 abnormal neurohypophysis morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0004201 fetal growth retardation IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1622332 Chtop chromatin target of PRMT1 gene MP:0004268 abnormal optic stalk morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0004603 absent vertebral arch IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0004607 abnormal cervical atlas morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0004646 decreased cervical vertebrae number IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0004648 decreased thoracic vertebrae number IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0005157 holoprosencephaly IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0005274 abnormal viscerocranium morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0006093 arteriovenous malformation IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0006107 abnormal fetal atrioventricular canal morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0008460 absent dorsal root ganglion IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 1622332 Chtop chromatin target of PRMT1 gene MP:0009804 abnormal brain interventricular foramen morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0009917 abnormal hyoid bone body morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0010404 ostium primum atrial septal defect IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0010406 common atrium IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0010440 anomalous pulmonary venous connection IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20190912 MGI PMID:29539633 1622332 Chtop chromatin target of PRMT1 gene MP:0010668 abnormal hepatic portal vein morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0010728 fusion of atlas and occipital bones IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0010977 fused right lung lobes IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 1622332 Chtop chromatin target of PRMT1 gene MP:0011361 pelvic kidney IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0011797 blind ureter IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0011974 intestinal stenosis IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0012548 myelocele IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013826 absent hypoglossal canal IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013842 ductus venosus stenosis IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013853 abnormal hepatic portal vein formation IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013855 absent celiac artery IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013857 abnormal abdominal muscle morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013858 abnormal azygos vein topology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013860 anastomosis between common carotid and vertebral artery IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013861 abnormal pancreas topology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013865 abnormal dorsal pancreas topology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013873 abnormal ductus venosus morphology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013878 abnormal ductus venosus valve topology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013913 absent costovertebral joint IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013915 abnormal brachial plexus formation IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013931 abnormal olfactory bulb position IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013943 abnormal ureter topology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013952 retroesophageal left subclavian artery IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013978 abnormal carotid artery origin IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013979 abnormal subclavian artery origin IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013987 absent intrahepatic inferior vena cava segment IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0013999 absent parasellar internal carotid artery IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0014002 absent extracranial vertebral artery segment IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0014019 embryo cyst IEA N RGD:5509061 20170504 MGI 1622332 Chtop chromatin target of PRMT1 gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20210422 MGI 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210422 MGI 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210422 MGI 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0001148 enlarged testis IEA N RGD:5509061 20210422 MGI 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:19177150 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:19177150 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210422 MGI 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210422 MGI 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210422 MGI 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:19177150 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20210422 MGI 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19177150 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210422 MGI 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:19177150 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20221103 MGI 1622333 Lamtor1 late endosomal/lysosomal adaptor, MAPK and MTOR activator 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 1622337 Golga7 golgin A7 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1622337 Golga7 golgin A7 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1622337 Golga7 golgin A7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622340 U90926 cDNA sequence U90926 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20231102 MGI PMID:36705532 1622340 U90926 cDNA sequence U90926 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20231102 MGI PMID:36705532 1622340 U90926 cDNA sequence U90926 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20231102 MGI PMID:36705532 1622343 Tro trophinin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11804944 1622343 Tro trophinin gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11804944 1622345 Cdca8 cell division cycle associated 8 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 1622345 Cdca8 cell division cycle associated 8 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 1622345 Cdca8 cell division cycle associated 8 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20160804 MGI 1622345 Cdca8 cell division cycle associated 8 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1622345 Cdca8 cell division cycle associated 8 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20160804 MGI 1622345 Cdca8 cell division cycle associated 8 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20160804 MGI 1622345 Cdca8 cell division cycle associated 8 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18337066 1622345 Cdca8 cell division cycle associated 8 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:18337066 1622345 Cdca8 cell division cycle associated 8 gene MP:0003707 increased cell nucleus count IAGP N RGD:5509061 20141003 MGI PMID:18337066 1622345 Cdca8 cell division cycle associated 8 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:18337066 1622345 Cdca8 cell division cycle associated 8 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18337066 1622345 Cdca8 cell division cycle associated 8 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18337066 1622345 Cdca8 cell division cycle associated 8 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18337066 1622349 Mink1 misshapen-like kinase 1 (zebrafish) gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20200514 MGI 1622349 Mink1 misshapen-like kinase 1 (zebrafish) gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20200514 MGI 1622349 Mink1 misshapen-like kinase 1 (zebrafish) gene MP:0001297 microphthalmia IEA N RGD:5509061 20200514 MGI 1622349 Mink1 misshapen-like kinase 1 (zebrafish) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20200514 MGI 1622349 Mink1 misshapen-like kinase 1 (zebrafish) gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20200514 MGI 1622349 Mink1 misshapen-like kinase 1 (zebrafish) gene MP:0002637 small uterus IEA N RGD:5509061 20200514 MGI 1622349 Mink1 misshapen-like kinase 1 (zebrafish) gene MP:0003068 enlarged kidney IEA N RGD:5509061 20200514 MGI 1622349 Mink1 misshapen-like kinase 1 (zebrafish) gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20201210 MGI PMID:26598717 1622349 Mink1 misshapen-like kinase 1 (zebrafish) gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20201210 MGI PMID:26598717 1622349 Mink1 misshapen-like kinase 1 (zebrafish) gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20201210 MGI PMID:26598717 1622349 Mink1 misshapen-like kinase 1 (zebrafish) gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20201210 MGI PMID:26598717 1622349 Mink1 misshapen-like kinase 1 (zebrafish) gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201210 MGI PMID:26598717 1622350 Exosc10 exosome component 10 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20201001 MGI PMID:32313933 1622350 Exosc10 exosome component 10 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20201001 MGI PMID:32313933 1622350 Exosc10 exosome component 10 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20201001 MGI PMID:32313933 1622350 Exosc10 exosome component 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 1622350 Exosc10 exosome component 10 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20201001 MGI PMID:32313933 1622350 Exosc10 exosome component 10 gene MP:0012128 abnormal blastocyst formation IAGP N RGD:5509061 20201001 MGI PMID:32313933 1622351 Il17rb interleukin 17 receptor B gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18768888 1622351 Il17rb interleukin 17 receptor B gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:22346732 1622351 Il17rb interleukin 17 receptor B gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:20200518 1622351 Il17rb interleukin 17 receptor B gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20200518 1622351 Il17rb interleukin 17 receptor B gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:20200518 1622351 Il17rb interleukin 17 receptor B gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:22346732 1622351 Il17rb interleukin 17 receptor B gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:20231694 1622351 Il17rb interleukin 17 receptor B gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20160526 MGI PMID:25888259 1622351 Il17rb interleukin 17 receptor B gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:22346732 1622351 Il17rb interleukin 17 receptor B gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:22346732 1622351 Il17rb interleukin 17 receptor B gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:18768888 1622351 Il17rb interleukin 17 receptor B gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:22346732 1622351 Il17rb interleukin 17 receptor B gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:22346732 1622351 Il17rb interleukin 17 receptor B gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:18768888 1622351 Il17rb interleukin 17 receptor B gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:20231694 1622351 Il17rb interleukin 17 receptor B gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:22346732 1622351 Il17rb interleukin 17 receptor B gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20231694 1622351 Il17rb interleukin 17 receptor B gene MP:0008712 decreased interleukin-9 secretion IAGP N RGD:5509061 20141003 MGI PMID:22346732 1622351 Il17rb interleukin 17 receptor B gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20231694 1622351 Il17rb interleukin 17 receptor B gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20160526 MGI PMID:25888259 1622352 Nrep neuronal regeneration related protein gene MP:0001440 abnormal grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:18616608 1622352 Nrep neuronal regeneration related protein gene MP:0001460 abnormal olfactory discrimination memory IAGP N RGD:5509061 20141003 MGI PMID:18616608 1622352 Nrep neuronal regeneration related protein gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:18616608 1622352 Nrep neuronal regeneration related protein gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:18616608 1622352 Nrep neuronal regeneration related protein gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:18616608 1622352 Nrep neuronal regeneration related protein gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:18616608 1622352 Nrep neuronal regeneration related protein gene MP:0002969 impaired social transmission of food preference IAGP N RGD:5509061 20141003 MGI PMID:18616608 1622352 Nrep neuronal regeneration related protein gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18616608 1622353 Fmnl3 formin-like 3 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 1622353 Fmnl3 formin-like 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1622353 Fmnl3 formin-like 3 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20161201 MGI 1622354 Vegfb vascular endothelial growth factor B gene MP:0000008 increased white adipose tissue amount IEA N RGD:5509061 20180222 MGI 1622354 Vegfb vascular endothelial growth factor B gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20210128 MGI 1622354 Vegfb vascular endothelial growth factor B gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12123775 1622354 Vegfb vascular endothelial growth factor B gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12123775 1622354 Vegfb vascular endothelial growth factor B gene MP:0001260 increased body weight IEA N RGD:5509061 20180222 MGI 1622354 Vegfb vascular endothelial growth factor B gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240627 MGI 1622354 Vegfb vascular endothelial growth factor B gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 1622354 Vegfb vascular endothelial growth factor B gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:10666423 1622354 Vegfb vascular endothelial growth factor B gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:21248239 1622354 Vegfb vascular endothelial growth factor B gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:10666423 1622354 Vegfb vascular endothelial growth factor B gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:10666423 1622354 Vegfb vascular endothelial growth factor B gene MP:0003039 increased time of peak ischemic contracture IAGP N RGD:5509061 20141003 MGI PMID:10666423 1622354 Vegfb vascular endothelial growth factor B gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 1622354 Vegfb vascular endothelial growth factor B gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:11457758 1622354 Vegfb vascular endothelial growth factor B gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:21248239 1622354 Vegfb vascular endothelial growth factor B gene MP:0003547 abnormal pulmonary pressure IAGP N RGD:5509061 20141003 MGI PMID:12123775 1622354 Vegfb vascular endothelial growth factor B gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:11457758 1622354 Vegfb vascular endothelial growth factor B gene MP:0003913 increased heart right ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:12123775 1622354 Vegfb vascular endothelial growth factor B gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:17051153 1622354 Vegfb vascular endothelial growth factor B gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20231207 MGI 1622354 Vegfb vascular endothelial growth factor B gene MP:0010755 abnormal heart right ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:12123775 1622354 Vegfb vascular endothelial growth factor B gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1622354 Vegfb vascular endothelial growth factor B gene MP:0020520 whitened brown adipose tissue morphology IEA N RGD:5509061 20180222 MGI 1622356 Vbp1 von Hippel-Lindau binding protein 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1622363 Vmn2r88 vomeronasal 2, receptor 88 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20190711 MGI PMID:30550786 1622369 Rn4.5s 4.5S RNA gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20240229 MGI PMID:38096826 1622369 Rn4.5s 4.5S RNA gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20240229 MGI PMID:38096826 1622370 Rmrp RNA component of mitochondrial RNAase P gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:22039455 1622370 Rmrp RNA component of mitochondrial RNAase P gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22039455 1622372 Slc50a1 solute carrier family 50 (sugar transporter), member 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1622372 Slc50a1 solute carrier family 50 (sugar transporter), member 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1622373 Bex1 brain expressed X-linked 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:17884015 1622373 Bex1 brain expressed X-linked 1 gene MP:0013237 abnormal skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:17884015 1622375 Ren2 renin 2 tandem duplication of Ren1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:8952610 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17330141 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:9697693 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:12796778 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:9697693 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:9697693 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17330141 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:9697693 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0000821 choroid plexus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23673330 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:9697693 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0000923 abnormal roof plate morphology IAGP N RGD:5509061 20141003 MGI PMID:23673330 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:11344260 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:16107726 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:23673330 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:13129914 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:13129914 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9697693 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10541472 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10541472 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:10541472 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23673330 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0001889 delayed brain development IAGP N RGD:5509061 20141003 MGI PMID:11344260 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0001889 delayed brain development IAGP N RGD:5509061 20141003 MGI PMID:9697693 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:13129914 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:13129914 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12796778 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0002208 abnormal germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:13129914 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:13129914 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16107726 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11344260 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:23673330 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20141003 MGI PMID:13129914 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12775763 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12775763 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:23673330 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:13129914 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12796778 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:16107726 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:23673330 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:23673330 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:13129914 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:13129914 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:13129914 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:17330141 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:9697693 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16107726 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:13129914 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23673330 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16107726 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9697693 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9697693 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23673330 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11344260 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0011155 absent hippocampus stratum oriens IAGP N RGD:5509061 20141003 MGI PMID:9697693 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:9697693 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12775763 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:12775763 1622377 Pafah1b1 platelet-activating factor acetylhydrolase, isoform 1b, subunit 1 gene MP:0021091 abnormal dorsal interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:23673330 1622378 Pabpc2 poly(A) binding protein, cytoplasmic 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20220224 MGI PMID:26971890 1622381 Slc25a15 solute carrier family 25 (mitochondrial carrier ornithine transporter), member 15 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1622381 Slc25a15 solute carrier family 25 (mitochondrial carrier ornithine transporter), member 15 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1622381 Slc25a15 solute carrier family 25 (mitochondrial carrier ornithine transporter), member 15 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1622381 Slc25a15 solute carrier family 25 (mitochondrial carrier ornithine transporter), member 15 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622383 Orm2 orosomucoid 2 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20240314 MGI PMID:36050503 1622383 Orm2 orosomucoid 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20240314 MGI PMID:36050503 1622383 Orm2 orosomucoid 2 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20201224 MGI PMID:32651445 1622383 Orm2 orosomucoid 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20240314 MGI PMID:36050503 1622383 Orm2 orosomucoid 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20240314 MGI PMID:36050503 1622383 Orm2 orosomucoid 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20240314 MGI PMID:36050503 1622383 Orm2 orosomucoid 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20240314 MGI PMID:36050503 1622383 Orm2 orosomucoid 2 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20240314 MGI PMID:36050503 1622383 Orm2 orosomucoid 2 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20201224 MGI PMID:32651445 1622383 Orm2 orosomucoid 2 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20240314 MGI PMID:36050503 1622383 Orm2 orosomucoid 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20240314 MGI PMID:36050503 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0004185 abnormal adipocyte glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:20733003 1622386 Mark3 MAP/microtubule affinity regulating kinase 3 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:20733003 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:15623425 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:11971016 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24239348 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20190912 MGI PMID:29844172 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12486099 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24239348 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20190912 MGI PMID:29844172 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11971016 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:12486099 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20160421 MGI 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17030606 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:15623425 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15623425 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:12486099 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20190912 MGI PMID:29844172 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:17885219 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0003991 arteriosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17885219 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20190912 MGI PMID:29844172 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17885219 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0005298 abnormal clavicle morphology IEA N RGD:5509061 20181227 MGI 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20210128 MGI 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12486099 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20190912 MGI PMID:29844172 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0008243 abnormal macrophage derived foam cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17885219 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20201022 MGI 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:10559880 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:10559880 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20190912 MGI PMID:29844172 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:11971016 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20190912 MGI PMID:29844172 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11971016 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:11971016 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20190912 MGI PMID:29844172 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:10559880 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20190912 MGI PMID:29844172 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:10559880 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11971016 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20190912 MGI PMID:29844172 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 1622387 Mapkapk2 MAP kinase-activated protein kinase 2 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:29844172 1622393 Magea4 MAGE family member A4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20240509 MGI PMID:31149633 1622393 Magea4 MAGE family member A4 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20240509 MGI PMID:31149633 1622393 Magea4 MAGE family member A4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20240509 MGI PMID:31149633 1622393 Magea4 MAGE family member A4 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240509 MGI PMID:31149633 1622393 Magea4 MAGE family member A4 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20240509 MGI PMID:31149633 1622397 Mab21l1 mab-21-like 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0002716 small male preputial gland IAGP N RGD:5509061 20141003 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0002717 abnormal male preputial gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20150416 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0005261 aniridia IAGP N RGD:5509061 20141003 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0009725 absent lens vesicle IAGP N RGD:5509061 20141003 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20160310 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0011964 increased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0012168 abnormal optic placode morphology IAGP N RGD:5509061 20141003 MGI PMID:12642482 1622397 Mab21l1 mab-21-like 1 gene MP:0013742 absent ciliary body IAGP N RGD:5509061 20150416 MGI PMID:12642482 1622399 Gfpt2 glutamine fructose-6-phosphate transaminase 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 1622399 Gfpt2 glutamine fructose-6-phosphate transaminase 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201231 MGI 1622399 Gfpt2 glutamine fructose-6-phosphate transaminase 2 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20170105 MGI 1622399 Gfpt2 glutamine fructose-6-phosphate transaminase 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 1622399 Gfpt2 glutamine fructose-6-phosphate transaminase 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 1622399 Gfpt2 glutamine fructose-6-phosphate transaminase 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1622399 Gfpt2 glutamine fructose-6-phosphate transaminase 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10631182 1622400 Gdf5 growth differentiation factor 5 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12606286 1622400 Gdf5 growth differentiation factor 5 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20230601 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:17656374 1622400 Gdf5 growth differentiation factor 5 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:12606286 1622400 Gdf5 growth differentiation factor 5 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17656374 1622400 Gdf5 growth differentiation factor 5 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:10631181 1622400 Gdf5 growth differentiation factor 5 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:125666 1622400 Gdf5 growth differentiation factor 5 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:5949834 1622400 Gdf5 growth differentiation factor 5 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:17656374 1622400 Gdf5 growth differentiation factor 5 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:908358 1622400 Gdf5 growth differentiation factor 5 gene MP:0000550 abnormal forelimb morphology IEA N RGD:5509061 20230601 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1622400 Gdf5 growth differentiation factor 5 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9012517 1622400 Gdf5 growth differentiation factor 5 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20190228 MGI PMID:8145850 1622400 Gdf5 growth differentiation factor 5 gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20230601 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:5949834 1622400 Gdf5 growth differentiation factor 5 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:5949834 1622400 Gdf5 growth differentiation factor 5 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:17085896 1622400 Gdf5 growth differentiation factor 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17085896 1622400 Gdf5 growth differentiation factor 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:908358 1622400 Gdf5 growth differentiation factor 5 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0001406 abnormal gait IEA N RGD:5509061 20230601 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0001513 limb grasping IEA N RGD:5509061 20230601 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0001922 reduced male fertility IEA N RGD:5509061 20141003 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17085896 1622400 Gdf5 growth differentiation factor 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12606286 1622400 Gdf5 growth differentiation factor 5 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:10631182 1622400 Gdf5 growth differentiation factor 5 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:5949834 1622400 Gdf5 growth differentiation factor 5 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:10631181 1622400 Gdf5 growth differentiation factor 5 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9012517 1622400 Gdf5 growth differentiation factor 5 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20190228 MGI PMID:8145850 1622400 Gdf5 growth differentiation factor 5 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10631181 1622400 Gdf5 growth differentiation factor 5 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:5949834 1622400 Gdf5 growth differentiation factor 5 gene MP:0002427 disproportionate dwarf IEA N RGD:5509061 20141003 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:10631182 1622400 Gdf5 growth differentiation factor 5 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:17085896 1622400 Gdf5 growth differentiation factor 5 gene MP:0002544 brachydactyly IEA N RGD:5509061 20141003 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20230601 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:5949834 1622400 Gdf5 growth differentiation factor 5 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:908358 1622400 Gdf5 growth differentiation factor 5 gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:5949834 1622400 Gdf5 growth differentiation factor 5 gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:908358 1622400 Gdf5 growth differentiation factor 5 gene MP:0002772 brachypodia IAGP N RGD:5509061 20141003 MGI PMID:17656374 1622400 Gdf5 growth differentiation factor 5 gene MP:0002772 brachypodia IAGP N RGD:5509061 20141003 MGI PMID:908358 1622400 Gdf5 growth differentiation factor 5 gene MP:0002772 brachypodia IAGP N RGD:5509061 20230824 MGI PMID:8145850 1622400 Gdf5 growth differentiation factor 5 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:125666 1622400 Gdf5 growth differentiation factor 5 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17656374 1622400 Gdf5 growth differentiation factor 5 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10631181 1622400 Gdf5 growth differentiation factor 5 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1622400 Gdf5 growth differentiation factor 5 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9012517 1622400 Gdf5 growth differentiation factor 5 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10631181 1622400 Gdf5 growth differentiation factor 5 gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9012517 1622400 Gdf5 growth differentiation factor 5 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:5949834 1622400 Gdf5 growth differentiation factor 5 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:908358 1622400 Gdf5 growth differentiation factor 5 gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:12606286 1622400 Gdf5 growth differentiation factor 5 gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:17656374 1622400 Gdf5 growth differentiation factor 5 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:125666 1622400 Gdf5 growth differentiation factor 5 gene MP:0003723 abnormal long bone morphology IEA N RGD:5509061 20111116 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:908358 1622400 Gdf5 growth differentiation factor 5 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:908358 1622400 Gdf5 growth differentiation factor 5 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:12606286 1622400 Gdf5 growth differentiation factor 5 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:908358 1622400 Gdf5 growth differentiation factor 5 gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:12606286 1622400 Gdf5 growth differentiation factor 5 gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1622400 Gdf5 growth differentiation factor 5 gene MP:0004602 abnormal vertebral articular process morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1622400 Gdf5 growth differentiation factor 5 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:10631182 1622400 Gdf5 growth differentiation factor 5 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20190228 MGI PMID:8145850 1622400 Gdf5 growth differentiation factor 5 gene MP:0004635 short metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:10631182 1622400 Gdf5 growth differentiation factor 5 gene MP:0004635 short metatarsal bones IAGP N RGD:5509061 20190228 MGI PMID:8145850 1622400 Gdf5 growth differentiation factor 5 gene MP:0004639 fused metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:10631182 1622400 Gdf5 growth differentiation factor 5 gene MP:0004642 fused metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:10631182 1622400 Gdf5 growth differentiation factor 5 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:17656374 1622400 Gdf5 growth differentiation factor 5 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:908358 1622400 Gdf5 growth differentiation factor 5 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20190228 MGI PMID:8145850 1622400 Gdf5 growth differentiation factor 5 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20230119 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9012517 1622400 Gdf5 growth differentiation factor 5 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20190228 MGI PMID:8145850 1622400 Gdf5 growth differentiation factor 5 gene MP:0005110 absent talus IAGP N RGD:5509061 20141003 MGI PMID:12606286 1622400 Gdf5 growth differentiation factor 5 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:10631181 1622400 Gdf5 growth differentiation factor 5 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:10631182 1622400 Gdf5 growth differentiation factor 5 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:12606286 1622400 Gdf5 growth differentiation factor 5 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:17085896 1622400 Gdf5 growth differentiation factor 5 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:17656374 1622400 Gdf5 growth differentiation factor 5 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:9012517 1622400 Gdf5 growth differentiation factor 5 gene MP:0005353 abnormal patella morphology IAGP N RGD:5509061 20141003 MGI PMID:9012517 1622400 Gdf5 growth differentiation factor 5 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:10631181 1622400 Gdf5 growth differentiation factor 5 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:908358 1622400 Gdf5 growth differentiation factor 5 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20190228 MGI PMID:8145850 1622400 Gdf5 growth differentiation factor 5 gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17656374 1622400 Gdf5 growth differentiation factor 5 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:5949834 1622400 Gdf5 growth differentiation factor 5 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:10631182 1622400 Gdf5 growth differentiation factor 5 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20190228 MGI PMID:8145850 1622400 Gdf5 growth differentiation factor 5 gene MP:0008736 micromelia IEA N RGD:5509061 20141003 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:9012517 1622400 Gdf5 growth differentiation factor 5 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:908358 1622400 Gdf5 growth differentiation factor 5 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0011261 abnormal limb mesenchyme morphology IAGP N RGD:5509061 20190228 MGI PMID:8145850 1622400 Gdf5 growth differentiation factor 5 gene MP:0011504 abnormal limb long bone morphology IEA N RGD:5509061 20141003 MGI 1622400 Gdf5 growth differentiation factor 5 gene MP:0030795 joint dislocation IAGP N RGD:5509061 20181025 MGI PMID:10631182 1622402 Gcsam germinal center associated, signaling and motility gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:16493007 1622402 Gcsam germinal center associated, signaling and motility gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:16493007 1622414 Pcdh15 protocadherin 15 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:15811708 1622414 Pcdh15 protocadherin 15 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20150716 MGI PMID:5093631 1622414 Pcdh15 protocadherin 15 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:10430593 1622414 Pcdh15 protocadherin 15 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:15811708 1622414 Pcdh15 protocadherin 15 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20150723 MGI PMID:5093631 1622414 Pcdh15 protocadherin 15 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10430593 1622414 Pcdh15 protocadherin 15 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:15811708 1622414 Pcdh15 protocadherin 15 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:16235133 1622414 Pcdh15 protocadherin 15 gene MP:0001394 circling IAGP N RGD:5509061 20160204 MGI PMID:16972005 1622414 Pcdh15 protocadherin 15 gene MP:0001394 circling IAGP N RGD:5509061 20220407 MGI PMID:16799054 1622414 Pcdh15 protocadherin 15 gene MP:0001394 circling IAGP N RGD:5509061 20231221 MGI PMID:34751129 1622414 Pcdh15 protocadherin 15 gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20220407 MGI PMID:16799054 1622414 Pcdh15 protocadherin 15 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20231221 MGI PMID:34751129 1622414 Pcdh15 protocadherin 15 gene MP:0001405 impaired coordination IEA N RGD:5509061 20141003 MGI 1622414 Pcdh15 protocadherin 15 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0001410 head bobbing IAGP N RGD:5509061 20160204 MGI PMID:16972005 1622414 Pcdh15 protocadherin 15 gene MP:0001410 head bobbing IAGP N RGD:5509061 20231221 MGI PMID:34751129 1622414 Pcdh15 protocadherin 15 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20231221 MGI PMID:34751129 1622414 Pcdh15 protocadherin 15 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:10430593 1622414 Pcdh15 protocadherin 15 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:15811708 1622414 Pcdh15 protocadherin 15 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:16235133 1622414 Pcdh15 protocadherin 15 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20220310 MGI PMID:15952048 1622414 Pcdh15 protocadherin 15 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:15811708 1622414 Pcdh15 protocadherin 15 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0001525 impaired balance IAGP N RGD:5509061 20160310 MGI PMID:24044941 1622414 Pcdh15 protocadherin 15 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15811708 1622414 Pcdh15 protocadherin 15 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20231221 MGI PMID:34751129 1622414 Pcdh15 protocadherin 15 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:16235133 1622414 Pcdh15 protocadherin 15 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:10430593 1622414 Pcdh15 protocadherin 15 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0001967 deafness IAGP N RGD:5509061 20150716 MGI PMID:5093631 1622414 Pcdh15 protocadherin 15 gene MP:0001967 deafness IAGP N RGD:5509061 20160204 MGI PMID:16972005 1622414 Pcdh15 protocadherin 15 gene MP:0001967 deafness IAGP N RGD:5509061 20160310 MGI PMID:24044941 1622414 Pcdh15 protocadherin 15 gene MP:0001967 deafness IAGP N RGD:5509061 20161216 MGI PMID:21427143 1622414 Pcdh15 protocadherin 15 gene MP:0001967 deafness IAGP N RGD:5509061 20220407 MGI PMID:16799054 1622414 Pcdh15 protocadherin 15 gene MP:0001967 deafness IAGP N RGD:5509061 20231221 MGI PMID:34751129 1622414 Pcdh15 protocadherin 15 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150716 MGI PMID:5093631 1622414 Pcdh15 protocadherin 15 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20150716 MGI PMID:5093631 1622414 Pcdh15 protocadherin 15 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20220407 MGI PMID:19816713 1622414 Pcdh15 protocadherin 15 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20150716 MGI PMID:5093631 1622414 Pcdh15 protocadherin 15 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:15537665 1622414 Pcdh15 protocadherin 15 gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20141003 MGI PMID:10430593 1622414 Pcdh15 protocadherin 15 gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20220310 MGI PMID:15952048 1622414 Pcdh15 protocadherin 15 gene MP:0002895 abnormal otolithic membrane morphology IAGP N RGD:5509061 20220310 MGI PMID:15952048 1622414 Pcdh15 protocadherin 15 gene MP:0003143 enlarged otoliths IAGP N RGD:5509061 20141003 MGI PMID:10430593 1622414 Pcdh15 protocadherin 15 gene MP:0003144 decreased otolith number IAGP N RGD:5509061 20220310 MGI PMID:15952048 1622414 Pcdh15 protocadherin 15 gene MP:0003151 absent tunnel of Corti IAGP N RGD:5509061 20150723 MGI PMID:5093631 1622414 Pcdh15 protocadherin 15 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15811708 1622414 Pcdh15 protocadherin 15 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0003637 cochlear ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20220407 MGI PMID:19816713 1622414 Pcdh15 protocadherin 15 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20220407 MGI PMID:16799054 1622414 Pcdh15 protocadherin 15 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20231221 MGI PMID:34751129 1622414 Pcdh15 protocadherin 15 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20220407 MGI PMID:16799054 1622414 Pcdh15 protocadherin 15 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20231221 MGI PMID:34751129 1622414 Pcdh15 protocadherin 15 gene MP:0004300 abnormal organ of Corti supporting cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0004303 abnormal Hensen cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20220310 MGI PMID:15952048 1622414 Pcdh15 protocadherin 15 gene MP:0004329 vestibular saccular degeneration IAGP N RGD:5509061 20220310 MGI PMID:15952048 1622414 Pcdh15 protocadherin 15 gene MP:0004331 vestibular saccular macula degeneration IAGP N RGD:5509061 20220310 MGI PMID:15952048 1622414 Pcdh15 protocadherin 15 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15537665 1622414 Pcdh15 protocadherin 15 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20160310 MGI PMID:24044941 1622414 Pcdh15 protocadherin 15 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20161216 MGI PMID:21427143 1622414 Pcdh15 protocadherin 15 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20231221 MGI PMID:34751129 1622414 Pcdh15 protocadherin 15 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15811708 1622414 Pcdh15 protocadherin 15 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20161216 MGI PMID:21427143 1622414 Pcdh15 protocadherin 15 gene MP:0004415 abnormal cochlear nerve compound action potential IEA N RGD:5509061 20141003 MGI 1622414 Pcdh15 protocadherin 15 gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20231221 MGI PMID:34751129 1622414 Pcdh15 protocadherin 15 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20161216 MGI PMID:21427143 1622414 Pcdh15 protocadherin 15 gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:11138007 1622414 Pcdh15 protocadherin 15 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20160310 MGI PMID:24044941 1622414 Pcdh15 protocadherin 15 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20220407 MGI PMID:16799054 1622414 Pcdh15 protocadherin 15 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:18339676 1622414 Pcdh15 protocadherin 15 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20220407 MGI PMID:16799054 1622414 Pcdh15 protocadherin 15 gene MP:0004524 short cochlear hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:11138007 1622414 Pcdh15 protocadherin 15 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15537665 1622414 Pcdh15 protocadherin 15 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15811708 1622414 Pcdh15 protocadherin 15 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 1622414 Pcdh15 protocadherin 15 gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20161216 MGI PMID:21427143 1622414 Pcdh15 protocadherin 15 gene MP:0004531 short outer hair cell stereocilia IEA N RGD:5509061 20141003 MGI 1622414 Pcdh15 protocadherin 15 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:11138007 1622414 Pcdh15 protocadherin 15 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15537665 1622414 Pcdh15 protocadherin 15 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15811708 1622414 Pcdh15 protocadherin 15 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 1622414 Pcdh15 protocadherin 15 gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20160310 MGI PMID:24044941 1622414 Pcdh15 protocadherin 15 gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20160310 MGI PMID:24044941 1622414 Pcdh15 protocadherin 15 gene MP:0004536 short inner hair cell stereocilia IEA N RGD:5509061 20141003 MGI 1622414 Pcdh15 protocadherin 15 gene MP:0004577 abnormal cochlear hair cell inter-stereocilial links morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 1622414 Pcdh15 protocadherin 15 gene MP:0004578 abnormal cochlear hair bundle tip links morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 1622414 Pcdh15 protocadherin 15 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20161216 MGI PMID:21427143 1622414 Pcdh15 protocadherin 15 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20141003 MGI 1622414 Pcdh15 protocadherin 15 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20220310 MGI PMID:15952048 1622414 Pcdh15 protocadherin 15 gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:15537665 1622414 Pcdh15 protocadherin 15 gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 1622414 Pcdh15 protocadherin 15 gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20220310 MGI PMID:15952048 1622414 Pcdh15 protocadherin 15 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20220407 MGI PMID:19816713 1622414 Pcdh15 protocadherin 15 gene MP:0005191 head tilt IEA N RGD:5509061 20111116 MGI 1622414 Pcdh15 protocadherin 15 gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0005307 head tossing IAGP N RGD:5509061 20220407 MGI PMID:16799054 1622414 Pcdh15 protocadherin 15 gene MP:0005323 dystonia IEA N RGD:5509061 20141003 MGI 1622414 Pcdh15 protocadherin 15 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20220407 MGI PMID:16799054 1622414 Pcdh15 protocadherin 15 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:10430593 1622414 Pcdh15 protocadherin 15 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20220310 MGI PMID:15952048 1622414 Pcdh15 protocadherin 15 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15811708 1622414 Pcdh15 protocadherin 15 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20220407 MGI PMID:16799054 1622414 Pcdh15 protocadherin 15 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20231221 MGI PMID:34751129 1622414 Pcdh15 protocadherin 15 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1622414 Pcdh15 protocadherin 15 gene MP:0010323 retropulsion IEA N RGD:5509061 20141003 MGI 1622414 Pcdh15 protocadherin 15 gene MP:0011039 abnormal vestibuloocular dark reflex IAGP N RGD:5509061 20220310 MGI PMID:15952048 1622414 Pcdh15 protocadherin 15 gene MP:0011040 abnormal vestibuloocular light reflex IAGP N RGD:5509061 20220310 MGI PMID:15952048 1622414 Pcdh15 protocadherin 15 gene MP:0011061 abnormal inner hair cell kinocilium morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 1622414 Pcdh15 protocadherin 15 gene MP:0011062 abnormal outer hair cell kinocilium morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 1622414 Pcdh15 protocadherin 15 gene MP:0011064 abnormal vestibular hair cell kinocilium morphology IAGP N RGD:5509061 20161216 MGI PMID:21427143 1622414 Pcdh15 protocadherin 15 gene MP:0011064 abnormal vestibular hair cell kinocilium morphology IAGP N RGD:5509061 20220407 MGI PMID:16799054 1622414 Pcdh15 protocadherin 15 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:10430593 1622414 Pcdh15 protocadherin 15 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11124469 1622414 Pcdh15 protocadherin 15 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15537665 1622414 Pcdh15 protocadherin 15 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15811708 1622414 Pcdh15 protocadherin 15 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16887306 1622414 Pcdh15 protocadherin 15 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:22381527 1622414 Pcdh15 protocadherin 15 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20161216 MGI PMID:21427143 1622414 Pcdh15 protocadherin 15 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20220407 MGI PMID:16799054 1622414 Pcdh15 protocadherin 15 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20220407 MGI PMID:16799054 1622414 Pcdh15 protocadherin 15 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20220407 MGI PMID:16799054 1622414 Pcdh15 protocadherin 15 gene MP:0030961 abnormal outer hair cell kinocilium location or orientation IAGP N RGD:5509061 20190725 MGI PMID:21427143 1622414 Pcdh15 protocadherin 15 gene MP:0030962 abnormal inner hair cell kinocilium location or orientation IAGP N RGD:5509061 20190725 MGI PMID:21427143 1622414 Pcdh15 protocadherin 15 gene MP:0030962 abnormal inner hair cell kinocilium location or orientation IAGP N RGD:5509061 20190725 MGI PMID:24044941 1622414 Pcdh15 protocadherin 15 gene MP:0031122 areflexia IAGP N RGD:5509061 20231221 MGI PMID:34751129 1622415 Atp6v1a ATPase, H+ transporting, lysosomal V1 subunit A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622417 Atp2a1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12556521 1622417 Atp2a1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12556521 1622417 Atp2a1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:12556521 1622417 Atp2a1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:12556521 1622417 Atp2a1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:12556521 1622417 Atp2a1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12556521 1622417 Atp2a1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1 gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:12556521 1622417 Atp2a1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1 gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:12556521 1622417 Atp2a1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12556521 1622417 Atp2a1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622507 Bod1l biorientation of chromosomes in cell division 1-like gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20231102 MGI PMID:35439434 1622507 Bod1l biorientation of chromosomes in cell division 1-like gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20231102 MGI PMID:35439434 1622507 Bod1l biorientation of chromosomes in cell division 1-like gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20231102 MGI PMID:35439434 1622535 Rbm46 RNA binding motif protein 46 gene MP:0001147 small testis IAGP N RGD:5509061 20221103 MGI PMID:36129965 1622535 Rbm46 RNA binding motif protein 46 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20221103 MGI PMID:36129965 1622535 Rbm46 RNA binding motif protein 46 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20221103 MGI PMID:36129965 1622535 Rbm46 RNA binding motif protein 46 gene MP:0001924 infertility IAGP N RGD:5509061 20221103 MGI PMID:36129965 1622535 Rbm46 RNA binding motif protein 46 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20221103 MGI PMID:36129965 1622535 Rbm46 RNA binding motif protein 46 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20221103 MGI PMID:36129965 1622535 Rbm46 RNA binding motif protein 46 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20221103 MGI PMID:36129965 1622550 Dact3 dishevelled-binding antagonist of beta-catenin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23580654 1622550 Dact3 dishevelled-binding antagonist of beta-catenin 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23580654 1622550 Dact3 dishevelled-binding antagonist of beta-catenin 3 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:23580654 1622550 Dact3 dishevelled-binding antagonist of beta-catenin 3 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23580654 1622550 Dact3 dishevelled-binding antagonist of beta-catenin 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1622550 Dact3 dishevelled-binding antagonist of beta-catenin 3 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:23580654 1622550 Dact3 dishevelled-binding antagonist of beta-catenin 3 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 1622550 Dact3 dishevelled-binding antagonist of beta-catenin 3 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160421 MGI 1622550 Dact3 dishevelled-binding antagonist of beta-catenin 3 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23580654 1622584 H2ab2 H2A.B variant histone 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20190627 MGI PMID:30704500 1622584 H2ab2 H2A.B variant histone 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20190627 MGI PMID:30704500 1622584 H2ab2 H2A.B variant histone 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20190627 MGI PMID:30704500 1622584 H2ab2 H2A.B variant histone 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20190627 MGI PMID:30704500 1622584 H2ab2 H2A.B variant histone 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20190627 MGI PMID:30704500 1622584 H2ab2 H2A.B variant histone 2 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20190627 MGI PMID:30704500 1622584 H2ab2 H2A.B variant histone 2 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20190627 MGI PMID:30704500 1622603 Gpr52 G protein-coupled receptor 52 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20150326 MGI PMID:24587241 1622603 Gpr52 G protein-coupled receptor 52 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20150326 MGI PMID:24587241 1622603 Gpr52 G protein-coupled receptor 52 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20150326 MGI PMID:24587241 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23238125 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:23238125 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:23238125 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:23238125 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:23238125 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23238125 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:23238125 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23238125 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:23238125 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23238125 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:23238125 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:23238125 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0010967 increased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:23238125 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0013617 increased areal bone mineral density IAGP N RGD:5509061 20220922 MGI PMID:23238125 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:23238125 1622604 Siglec15 sialic acid binding Ig-like lectin 15 gene MP:0030984 increased circulating osteocalcin level IAGP N RGD:5509061 20191219 MGI PMID:23238125 1622608 Btnl2 butyrophilin-like 2 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20220317 MGI PMID:35017553 1622608 Btnl2 butyrophilin-like 2 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20220317 MGI PMID:35017553 1622608 Btnl2 butyrophilin-like 2 gene MP:0008343 abnormal gamma-delta T cell morphology IAGP N RGD:5509061 20220317 MGI PMID:35017553 1622608 Btnl2 butyrophilin-like 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20220317 MGI PMID:35017553 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0000692 small spleen IEA N RGD:5509061 20210826 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20210826 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20210826 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20210826 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210826 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20220519 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20221215 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0011045 decreased lung elastance IEA N RGD:5509061 20221215 MGI 1622615 Fbxw18 F-box and WD-40 domain protein 18 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1622616 Fbxw25 F-box and WD-40 domain protein 25 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1622616 Fbxw25 F-box and WD-40 domain protein 25 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1622616 Fbxw25 F-box and WD-40 domain protein 25 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1622616 Fbxw25 F-box and WD-40 domain protein 25 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1622619 Wdr72 WD repeat domain 72 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150910 MGI PMID:25008349 1622619 Wdr72 WD repeat domain 72 gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20150910 MGI PMID:25008349 1622619 Wdr72 WD repeat domain 72 gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20150910 MGI PMID:25008349 1622619 Wdr72 WD repeat domain 72 gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20150910 MGI PMID:25008349 1622619 Wdr72 WD repeat domain 72 gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20180215 MGI PMID:25008349 1622620 Pierce2 piercer of microtubule wall 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20240523 MGI 1622620 Pierce2 piercer of microtubule wall 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20220120 MGI PMID:34715025 1622620 Pierce2 piercer of microtubule wall 2 gene MP:0002766 situs inversus IAGP N RGD:5509061 20220120 MGI PMID:34715025 1622620 Pierce2 piercer of microtubule wall 2 gene MP:0002767 situs ambiguus IAGP N RGD:5509061 20220120 MGI PMID:34715025 1622620 Pierce2 piercer of microtubule wall 2 gene MP:0003900 shortened QT interval IEA N RGD:5509061 20230601 MGI 1622620 Pierce2 piercer of microtubule wall 2 gene MP:0008933 abnormal motile primary cilium physiology IAGP N RGD:5509061 20220120 MGI PMID:34715025 1622620 Pierce2 piercer of microtubule wall 2 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20230601 MGI 1622620 Pierce2 piercer of microtubule wall 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20220120 MGI PMID:34715025 1622620 Pierce2 piercer of microtubule wall 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20220120 MGI PMID:34715025 1622621 Gramd2a GRAM domain containing 2A gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 1622621 Gramd2a GRAM domain containing 2A gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 1622621 Gramd2a GRAM domain containing 2A gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20230601 MGI 1622621 Gramd2a GRAM domain containing 2A gene MP:0002637 small uterus IEA N RGD:5509061 20230601 MGI 1622621 Gramd2a GRAM domain containing 2A gene MP:0004609 vertebral fusion IEA N RGD:5509061 20230601 MGI 1622621 Gramd2a GRAM domain containing 2A gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20230601 MGI 1622639 Fcrlb Fc receptor-like B gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:20869045 1622639 Fcrlb Fc receptor-like B gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20869045 1622643 Rufy4 RUN and FYVE domain containing 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1622643 Rufy4 RUN and FYVE domain containing 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 1622643 Rufy4 RUN and FYVE domain containing 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1622643 Rufy4 RUN and FYVE domain containing 4 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 1622656 Nlrc5 NLR family, CARD domain containing 5 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22412192 1622656 Nlrc5 NLR family, CARD domain containing 5 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22412192 1622656 Nlrc5 NLR family, CARD domain containing 5 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22412192 1622656 Nlrc5 NLR family, CARD domain containing 5 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22645137 1622656 Nlrc5 NLR family, CARD domain containing 5 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:22645137 1622660 Ly6g6f lymphocyte antigen 6 family member G6F gene MP:0005333 decreased heart rate IEA N RGD:5509061 20230601 MGI 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001190 reddish skin IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001196 shiny skin IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001196 shiny skin IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001196 shiny skin IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001198 tight skin IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001198 tight skin IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001230 epidermal desquamation IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001257 increased body length IEA N RGD:5509061 20201022 MGI 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001874 acanthosis IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0001874 acanthosis IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0003773 eclabion IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0003853 dry skin IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0009596 abnormal stratum corneum lipid matrix formation IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0009597 impaired stratum corneum desquamation IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0009597 impaired stratum corneum desquamation IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0009602 abnormal keratohyalin granule morphology IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0009605 decreased keratohyalin granule number IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0009605 decreased keratohyalin granule number IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0009607 decreased keratohyalin granule size IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0009823 abnormal sphingomyelin level IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0010358 abnormal free fatty acids level IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0010358 abnormal free fatty acids level IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0012232 abnormal ceramide level IAGP N RGD:5509061 20190425 MGI PMID:28369476 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0013177 abnormal tail tip morphology IAGP N RGD:5509061 20170803 MGI PMID:27751867 1622661 Pnpla1 patatin-like phospholipase domain containing 1 gene MP:0013177 abnormal tail tip morphology IAGP N RGD:5509061 20170824 MGI PMID:28248300 1622676 Zyg11b zyg-ll family member B, cell cycle regulator gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1622676 Zyg11b zyg-ll family member B, cell cycle regulator gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1622676 Zyg11b zyg-ll family member B, cell cycle regulator gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1622677 Itprip inositol 1,4,5-triphosphate receptor interacting protein gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20053891 1622677 Itprip inositol 1,4,5-triphosphate receptor interacting protein gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:20053891 1622677 Itprip inositol 1,4,5-triphosphate receptor interacting protein gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:20053891 1622768 Opa3 optic atrophy 3 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0011015 decreased body surface temperature IAGP N RGD:5509061 20141003 MGI PMID:22869679 1622768 Opa3 optic atrophy 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18222992 1622768 Opa3 optic atrophy 3 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:22869679 1622775 Msantd1 Myb/SANT-like DNA-binding domain containing 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20160811 MGI 1622775 Msantd1 Myb/SANT-like DNA-binding domain containing 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20160811 MGI 1622775 Msantd1 Myb/SANT-like DNA-binding domain containing 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1622781 Znrf2 zinc and ring finger 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1622795 Aim2 absent in melanoma 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20170223 MGI PMID:26114879 1622795 Aim2 absent in melanoma 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170223 MGI PMID:26114879 1622795 Aim2 absent in melanoma 2 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 1622795 Aim2 absent in melanoma 2 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 1622795 Aim2 absent in melanoma 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20351692 1622795 Aim2 absent in melanoma 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20457908 1622795 Aim2 absent in melanoma 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:22695634 1622795 Aim2 absent in melanoma 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20351692 1622795 Aim2 absent in melanoma 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20457908 1622795 Aim2 absent in melanoma 2 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20210826 MGI 1622795 Aim2 absent in melanoma 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20457908 1622795 Aim2 absent in melanoma 2 gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20170223 MGI PMID:26114879 1622795 Aim2 absent in melanoma 2 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20170223 MGI PMID:26114879 1622795 Aim2 absent in melanoma 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20170223 MGI PMID:26114879 1622795 Aim2 absent in melanoma 2 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20210826 MGI 1622795 Aim2 absent in melanoma 2 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210826 MGI 1622795 Aim2 absent in melanoma 2 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:20351692 1622795 Aim2 absent in melanoma 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20170223 MGI PMID:26114879 1622795 Aim2 absent in melanoma 2 gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20160915 MGI PMID:27496731 1622795 Aim2 absent in melanoma 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20457908 1622795 Aim2 absent in melanoma 2 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20351692 1622795 Aim2 absent in melanoma 2 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20457908 1622795 Aim2 absent in melanoma 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22695634 1622795 Aim2 absent in melanoma 2 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20170223 MGI PMID:26114879 1622795 Aim2 absent in melanoma 2 gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:20351692 1622795 Aim2 absent in melanoma 2 gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:22695634 1622795 Aim2 absent in melanoma 2 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20351692 1622795 Aim2 absent in melanoma 2 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20457908 1622795 Aim2 absent in melanoma 2 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22695634 1622795 Aim2 absent in melanoma 2 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20160915 MGI PMID:27496731 1622795 Aim2 absent in melanoma 2 gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:20351692 1622795 Aim2 absent in melanoma 2 gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:20457908 1622795 Aim2 absent in melanoma 2 gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:22695634 1622795 Aim2 absent in melanoma 2 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20210826 MGI 1622795 Aim2 absent in melanoma 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22695634 1622795 Aim2 absent in melanoma 2 gene MP:0011081 decreased macrophage apoptosis IAGP N RGD:5509061 20160915 MGI PMID:27496731 1622795 Aim2 absent in melanoma 2 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:20351692 1622795 Aim2 absent in melanoma 2 gene MP:0020928 increased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:20351692 1622798 Cimap1d CIMAP1 family member D gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20231207 MGI 1622798 Cimap1d CIMAP1 family member D gene MP:0000274 enlarged heart IEA N RGD:5509061 20231207 MGI 1622798 Cimap1d CIMAP1 family member D gene MP:0001284 absent vibrissae IEA N RGD:5509061 20231207 MGI 1622798 Cimap1d CIMAP1 family member D gene MP:0001406 abnormal gait IEA N RGD:5509061 20231207 MGI 1622798 Cimap1d CIMAP1 family member D gene MP:0001410 head bobbing IEA N RGD:5509061 20231207 MGI 1622798 Cimap1d CIMAP1 family member D gene MP:0001523 impaired righting response IEA N RGD:5509061 20231207 MGI 1622798 Cimap1d CIMAP1 family member D gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20231207 MGI 1622798 Cimap1d CIMAP1 family member D gene MP:0003068 enlarged kidney IEA N RGD:5509061 20231207 MGI 1622798 Cimap1d CIMAP1 family member D gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 1622805 Ccdc78 coiled-coil domain containing 78 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20230601 MGI 1622807 Abca17 ATP-binding cassette, sub-family A member 17 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1622807 Abca17 ATP-binding cassette, sub-family A member 17 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20210128 MGI 1622815 Mix23 mitochondrial matrix import factor 23 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38786026 1622820 Pram1 PML-RAR alpha-regulated adaptor molecule 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:15572693 1622820 Pram1 PML-RAR alpha-regulated adaptor molecule 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1622821 Nanos2 nanos C2HC-type zinc finger 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16806845 1622821 Nanos2 nanos C2HC-type zinc finger 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12947200 1622821 Nanos2 nanos C2HC-type zinc finger 2 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:18281459 1622821 Nanos2 nanos C2HC-type zinc finger 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16806845 1622821 Nanos2 nanos C2HC-type zinc finger 2 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:24183939 1622821 Nanos2 nanos C2HC-type zinc finger 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12947200 1622821 Nanos2 nanos C2HC-type zinc finger 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:16806845 1622821 Nanos2 nanos C2HC-type zinc finger 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:12947200 1622821 Nanos2 nanos C2HC-type zinc finger 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:18281459 1622821 Nanos2 nanos C2HC-type zinc finger 2 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:24183939 1622821 Nanos2 nanos C2HC-type zinc finger 2 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1622821 Nanos2 nanos C2HC-type zinc finger 2 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18281459 1622821 Nanos2 nanos C2HC-type zinc finger 2 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18281459 1622821 Nanos2 nanos C2HC-type zinc finger 2 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20200514 MGI 1622822 Nlrp12 NLR family, pyrin domain containing 12 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20861349 1622822 Nlrp12 NLR family, pyrin domain containing 12 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22094258 1622822 Nlrp12 NLR family, pyrin domain containing 12 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22094258 1622822 Nlrp12 NLR family, pyrin domain containing 12 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:20861349 1622822 Nlrp12 NLR family, pyrin domain containing 12 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22094258 1622822 Nlrp12 NLR family, pyrin domain containing 12 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:20861349 1622822 Nlrp12 NLR family, pyrin domain containing 12 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:22094258 1622822 Nlrp12 NLR family, pyrin domain containing 12 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:22094258 1622822 Nlrp12 NLR family, pyrin domain containing 12 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20861349 1622822 Nlrp12 NLR family, pyrin domain containing 12 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:22094258 1622827 Defb34 defensin beta 34 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1622827 Defb34 defensin beta 34 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20240627 MGI 1622830 Zmynd12 zinc finger, MYND domain containing 12 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20240523 MGI 1622830 Zmynd12 zinc finger, MYND domain containing 12 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 1622830 Zmynd12 zinc finger, MYND domain containing 12 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1622830 Zmynd12 zinc finger, MYND domain containing 12 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20240523 MGI 1622830 Zmynd12 zinc finger, MYND domain containing 12 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 1622830 Zmynd12 zinc finger, MYND domain containing 12 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1622830 Zmynd12 zinc finger, MYND domain containing 12 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1622831 Bend3 BEN domain containing 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20170105 MGI 1622831 Bend3 BEN domain containing 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622834 Mindy4 MINDY lysine 48 deubiquitinase 4 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20190502 MGI 1622835 Wipf3 WAS/WASL interacting protein family, member 3 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:17573773 1622835 Wipf3 WAS/WASL interacting protein family, member 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17573773 1622835 Wipf3 WAS/WASL interacting protein family, member 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17573773 1622835 Wipf3 WAS/WASL interacting protein family, member 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17573773 1622835 Wipf3 WAS/WASL interacting protein family, member 3 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17573773 1622835 Wipf3 WAS/WASL interacting protein family, member 3 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17573773 1622835 Wipf3 WAS/WASL interacting protein family, member 3 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:17573773 1622835 Wipf3 WAS/WASL interacting protein family, member 3 gene MP:0009235 small sperm head IAGP N RGD:5509061 20141003 MGI PMID:17573773 1622839 Pkd2l1 polycystic kidney disease 2-like 1 gene MP:0001985 abnormal gustatory system physiology IAGP N RGD:5509061 20141003 MGI PMID:21625513 1622839 Pkd2l1 polycystic kidney disease 2-like 1 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:21625513 1622843 Usp44 ubiquitin specific peptidase 44 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23187126 1622843 Usp44 ubiquitin specific peptidase 44 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23187126 1622843 Usp44 ubiquitin specific peptidase 44 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23187126 1622843 Usp44 ubiquitin specific peptidase 44 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:23187126 1622843 Usp44 ubiquitin specific peptidase 44 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:23187126 1622843 Usp44 ubiquitin specific peptidase 44 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:23187126 1622843 Usp44 ubiquitin specific peptidase 44 gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23187126 1622843 Usp44 ubiquitin specific peptidase 44 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23187126 1622845 Tmem26 transmembrane protein 26 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210415 MGI PMID:21980401 1622846 Dna2 DNA replication helicase/nuclease 2 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20200310 MGI PMID:23604072 1622846 Dna2 DNA replication helicase/nuclease 2 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20200310 MGI PMID:23604072 1622846 Dna2 DNA replication helicase/nuclease 2 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20200310 MGI PMID:23604072 1622846 Dna2 DNA replication helicase/nuclease 2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200310 MGI PMID:23604072 1622846 Dna2 DNA replication helicase/nuclease 2 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20200310 MGI PMID:23604072 1622846 Dna2 DNA replication helicase/nuclease 2 gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20200310 MGI PMID:23604072 1622846 Dna2 DNA replication helicase/nuclease 2 gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20200310 MGI PMID:23604072 1622846 Dna2 DNA replication helicase/nuclease 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23604072 1622846 Dna2 DNA replication helicase/nuclease 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:23604072 1622846 Dna2 DNA replication helicase/nuclease 2 gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20200310 MGI PMID:23604072 1622847 Mettl24 methyltransferase like 24 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 1622847 Mettl24 methyltransferase like 24 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150108 MGI 1622847 Mettl24 methyltransferase like 24 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 1622847 Mettl24 methyltransferase like 24 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 1622847 Mettl24 methyltransferase like 24 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 1622848 Ccn6 cellular communication network factor 6 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20171214 MGI PMID:27819674 1622848 Ccn6 cellular communication network factor 6 gene MP:0001147 small testis IAGP N RGD:5509061 20220707 MGI PMID:34518881 1622848 Ccn6 cellular communication network factor 6 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20171214 MGI PMID:27819674 1622848 Ccn6 cellular communication network factor 6 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20171214 MGI PMID:27819674 1622848 Ccn6 cellular communication network factor 6 gene MP:0001885 mammary gland duct hyperplasia IAGP N RGD:5509061 20171214 MGI PMID:27819674 1622848 Ccn6 cellular communication network factor 6 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220707 MGI PMID:34518881 1622848 Ccn6 cellular communication network factor 6 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220707 MGI PMID:34518881 1622848 Ccn6 cellular communication network factor 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15601861 1622848 Ccn6 cellular communication network factor 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24040393 1622848 Ccn6 cellular communication network factor 6 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20220707 MGI PMID:34518881 1622848 Ccn6 cellular communication network factor 6 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220707 MGI PMID:34518881 1622848 Ccn6 cellular communication network factor 6 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20220707 MGI PMID:34518881 1622848 Ccn6 cellular communication network factor 6 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220707 MGI PMID:34518881 1622848 Ccn6 cellular communication network factor 6 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220707 MGI PMID:34518881 1622848 Ccn6 cellular communication network factor 6 gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20171214 MGI PMID:27819674 1622848 Ccn6 cellular communication network factor 6 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220707 MGI PMID:34518881 1622848 Ccn6 cellular communication network factor 6 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220707 MGI PMID:34518881 1622848 Ccn6 cellular communication network factor 6 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20171214 MGI PMID:27819674 1622848 Ccn6 cellular communication network factor 6 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220707 MGI PMID:34518881 1622848 Ccn6 cellular communication network factor 6 gene MP:0009839 multiflagellated sperm IAGP N RGD:5509061 20220707 MGI PMID:34518881 1622848 Ccn6 cellular communication network factor 6 gene MP:0013782 abnormal mammary duct terminal end bud morphology IAGP N RGD:5509061 20171214 MGI PMID:27819674 1622848 Ccn6 cellular communication network factor 6 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220707 MGI PMID:34518881 1622848 Ccn6 cellular communication network factor 6 gene MP:0031427 increased sperm progressive motility IAGP N RGD:5509061 20220714 MGI PMID:34518881 1622851 Auts2 autism susceptibility candidate 2 gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20180628 MGI 1622851 Auts2 autism susceptibility candidate 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20151217 MGI PMID:25519132 1622851 Auts2 autism susceptibility candidate 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180531 MGI PMID:26717414 1622851 Auts2 autism susceptibility candidate 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20180531 MGI PMID:26717414 1622851 Auts2 autism susceptibility candidate 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20180531 MGI PMID:26717414 1622851 Auts2 autism susceptibility candidate 2 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20180531 MGI PMID:26717414 1622851 Auts2 autism susceptibility candidate 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20151217 MGI PMID:25519132 1622851 Auts2 autism susceptibility candidate 2 gene MP:0002947 increased hemangioma incidence IEA N RGD:5509061 20210930 MGI 1622851 Auts2 autism susceptibility candidate 2 gene MP:0003266 biliary cyst IEA N RGD:5509061 20180628 MGI 1622851 Auts2 autism susceptibility candidate 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20180531 MGI PMID:25533347 1622851 Auts2 autism susceptibility candidate 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1622851 Auts2 autism susceptibility candidate 2 gene MP:0005356 positive geotaxis IAGP N RGD:5509061 20151217 MGI PMID:25519132 1622851 Auts2 autism susceptibility candidate 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20180531 MGI PMID:25533347 1622851 Auts2 autism susceptibility candidate 2 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20180628 MGI 1622851 Auts2 autism susceptibility candidate 2 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20180531 MGI PMID:26717414 1622851 Auts2 autism susceptibility candidate 2 gene MP:0010726 abnormal collateral sprouting IAGP N RGD:5509061 20180531 MGI PMID:25533347 1622851 Auts2 autism susceptibility candidate 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180531 MGI PMID:25533347 1622851 Auts2 autism susceptibility candidate 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622851 Auts2 autism susceptibility candidate 2 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20180531 MGI PMID:26717414 1622851 Auts2 autism susceptibility candidate 2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20151217 MGI PMID:25519132 1622851 Auts2 autism susceptibility candidate 2 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20180628 MGI 1622851 Auts2 autism susceptibility candidate 2 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20180628 MGI 1622851 Auts2 autism susceptibility candidate 2 gene MP:0013852 abnormal Mullerian duct topology IEA N RGD:5509061 20180628 MGI 1622851 Auts2 autism susceptibility candidate 2 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20180628 MGI 1622851 Auts2 autism susceptibility candidate 2 gene MP:0014018 embryo tumor IEA N RGD:5509061 20180628 MGI 1622851 Auts2 autism susceptibility candidate 2 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:26717414 1622851 Auts2 autism susceptibility candidate 2 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:25519132 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000548 long limbs IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:22393014 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001202 skin photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:9150142 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9150142 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:9150142 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22393014 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:9150142 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22393014 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9150142 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22393014 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:22393014 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22393014 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:9150142 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22393014 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0001999 photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:9150142 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:9150142 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:22393014 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20151210 MGI PMID:25762674 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20151210 MGI PMID:25762674 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20151210 MGI PMID:25762674 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0004586 pillar cell degeneration IAGP N RGD:5509061 20151210 MGI PMID:25762674 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0004628 Deiters cell degeneration IAGP N RGD:5509061 20151210 MGI PMID:25762674 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:22393014 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9150142 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20151210 MGI PMID:25762674 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:9150142 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22393014 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0009796 abnormal base-excision repair IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22393014 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22174697 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20141003 MGI PMID:17326724 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20151210 MGI PMID:25762674 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0013551 decreased cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20161201 MGI PMID:11687625 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0013787 photophobia IAGP N RGD:5509061 20150611 MGI PMID:9150142 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0014409 decreased distortion product otoacoustic emission amplitude IAGP N RGD:5509061 20240405 MGI PMID:25762674 1622854 Ercc6 excision repair cross-complementing rodent repair deficiency, complementation group 6 gene MP:0030003 hippocampus atrophy IAGP N RGD:5509061 20170706 MGI PMID:22174697 1622856 Taf2 TATA-box binding protein associated factor 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1622856 Taf2 TATA-box binding protein associated factor 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240627 MGI 1622856 Taf2 TATA-box binding protein associated factor 2 gene MP:0004357 long tibia IEA N RGD:5509061 20201022 MGI 1622856 Taf2 TATA-box binding protein associated factor 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1622856 Taf2 TATA-box binding protein associated factor 2 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20201022 MGI 1622856 Taf2 TATA-box binding protein associated factor 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 1622856 Taf2 TATA-box binding protein associated factor 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622858 Tns3 tensin 3 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20220811 MGI 1622858 Tns3 tensin 3 gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20221215 MGI 1622858 Tns3 tensin 3 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20200310 MGI PMID:15733665 1622858 Tns3 tensin 3 gene MP:0000692 small spleen IAGP N RGD:5509061 20200310 MGI PMID:15733665 1622858 Tns3 tensin 3 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:15733665 1622858 Tns3 tensin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:15733665 1622858 Tns3 tensin 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:15733665 1622858 Tns3 tensin 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:15733665 1622858 Tns3 tensin 3 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20200310 MGI PMID:15733665 1622858 Tns3 tensin 3 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20200310 MGI PMID:15733665 1622858 Tns3 tensin 3 gene MP:0002691 small stomach IAGP N RGD:5509061 20200310 MGI PMID:15733665 1622858 Tns3 tensin 3 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20200310 MGI PMID:15733665 1622858 Tns3 tensin 3 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20200310 MGI PMID:15733665 1622858 Tns3 tensin 3 gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20240523 MGI 1622858 Tns3 tensin 3 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20200310 MGI PMID:15733665 1622858 Tns3 tensin 3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210826 MGI 1622858 Tns3 tensin 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1622858 Tns3 tensin 3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 1622858 Tns3 tensin 3 gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20200310 MGI PMID:15733665 1622859 Sbf2 SET binding factor 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:17855448 1622859 Sbf2 SET binding factor 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20200310 MGI PMID:18349142 1622859 Sbf2 SET binding factor 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:17855448 1622859 Sbf2 SET binding factor 2 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:17855448 1622859 Sbf2 SET binding factor 2 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20200310 MGI PMID:17855448 1622859 Sbf2 SET binding factor 2 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20200310 MGI PMID:18349142 1622859 Sbf2 SET binding factor 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20220811 MGI PMID:34718573 1622859 Sbf2 SET binding factor 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200310 MGI PMID:17855448 1622859 Sbf2 SET binding factor 2 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20200310 MGI PMID:18349142 1622859 Sbf2 SET binding factor 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200310 MGI PMID:17855448 1622859 Sbf2 SET binding factor 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20220811 MGI PMID:34718573 1622862 Ism1 isthmin 1, angiogenesis inhibitor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20211209 MGI PMID:34348115 1622862 Ism1 isthmin 1, angiogenesis inhibitor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20211209 MGI PMID:34348115 1622863 9630013A20Rik RIKEN cDNA 9630013A20 gene gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20180607 MGI PMID:28041882 1622863 9630013A20Rik RIKEN cDNA 9630013A20 gene gene MP:0013438 dysmyelination IAGP N RGD:5509061 20180607 MGI PMID:28041882 1622864 Pcdh19 protocadherin 19 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20180308 MGI PMID:29301106 1622864 Pcdh19 protocadherin 19 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20180308 MGI PMID:29301106 1622864 Pcdh19 protocadherin 19 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20180308 MGI PMID:27240640 1622867 Zfp385c zinc finger protein 385C gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20240523 MGI 1622867 Zfp385c zinc finger protein 385C gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1622867 Zfp385c zinc finger protein 385C gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1622867 Zfp385c zinc finger protein 385C gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 1622869 Rbbp8nl RBBP8 N-terminal like gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 1622869 Rbbp8nl RBBP8 N-terminal like gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 1622870 Pla2g4f phospholipase A2, group IVF gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160804 MGI 1622871 Ct45a cancer/testis antigen 45 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20230601 MGI 1622871 Ct45a cancer/testis antigen 45 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1622871 Ct45a cancer/testis antigen 45 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1622872 Setx senataxin gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210128 MGI 1622872 Setx senataxin gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 1622872 Setx senataxin gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20201022 MGI 1622872 Setx senataxin gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20220310 MGI PMID:29725819 1622872 Setx senataxin gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20220310 MGI PMID:29725819 1622872 Setx senataxin gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20220310 MGI PMID:29725819 1622872 Setx senataxin gene MP:0001147 small testis IAGP N RGD:5509061 20151210 MGI PMID:23593030 1622872 Setx senataxin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20220310 MGI PMID:29725819 1622872 Setx senataxin gene MP:0001513 limb grasping IAGP N RGD:5509061 20220310 MGI PMID:29725819 1622872 Setx senataxin gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20151210 MGI PMID:23593030 1622872 Setx senataxin gene MP:0001925 male infertility IAGP N RGD:5509061 20151210 MGI PMID:23593030 1622872 Setx senataxin gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20151210 MGI PMID:23593030 1622872 Setx senataxin gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20220310 MGI PMID:29725819 1622872 Setx senataxin gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20151210 MGI PMID:23593030 1622872 Setx senataxin gene MP:0002686 globozoospermia IAGP N RGD:5509061 20151210 MGI PMID:23593030 1622872 Setx senataxin gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20220310 MGI PMID:29725819 1622872 Setx senataxin gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20210128 MGI 1622872 Setx senataxin gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20160421 MGI 1622872 Setx senataxin gene MP:0005159 azoospermia IAGP N RGD:5509061 20151210 MGI PMID:23593030 1622872 Setx senataxin gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20151210 MGI PMID:23593030 1622872 Setx senataxin gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 1622872 Setx senataxin gene MP:0008044 increased NK cell number IEA N RGD:5509061 20210128 MGI 1622872 Setx senataxin gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20220310 MGI PMID:29725819 1622872 Setx senataxin gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20151210 MGI PMID:23593030 1622872 Setx senataxin gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20151210 MGI PMID:23593030 1622872 Setx senataxin gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20151210 MGI PMID:23593030 1622872 Setx senataxin gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1622872 Setx senataxin gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:23593030 1622875 Cyb5r4 cytochrome b5 reductase 4 gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20200310 MGI PMID:15247412 1622875 Cyb5r4 cytochrome b5 reductase 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20200310 MGI PMID:15247412 1622875 Cyb5r4 cytochrome b5 reductase 4 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:15247412 1622875 Cyb5r4 cytochrome b5 reductase 4 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200310 MGI PMID:15247412 1622875 Cyb5r4 cytochrome b5 reductase 4 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:15247412 1622875 Cyb5r4 cytochrome b5 reductase 4 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20200310 MGI PMID:15247412 1622875 Cyb5r4 cytochrome b5 reductase 4 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20200310 MGI PMID:15247412 1622875 Cyb5r4 cytochrome b5 reductase 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:15247412 1622875 Cyb5r4 cytochrome b5 reductase 4 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:15247412 1622875 Cyb5r4 cytochrome b5 reductase 4 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:15247412 1622875 Cyb5r4 cytochrome b5 reductase 4 gene MP:0011939 increased food intake IAGP N RGD:5509061 20200310 MGI PMID:15247412 1622877 Ly6g5b lymphocyte antigen 6 family member G5B gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20240523 MGI 1622877 Ly6g5b lymphocyte antigen 6 family member G5B gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201231 MGI 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201231 MGI PMID:31509750 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20201231 MGI 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20201231 MGI PMID:31509750 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20201231 MGI PMID:31509750 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20201231 MGI PMID:31509750 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20201231 MGI 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20201231 MGI PMID:31509750 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20201231 MGI PMID:31509750 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20201231 MGI PMID:31509750 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20201231 MGI PMID:31509750 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:17620419 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17620419 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0012111 failure of morula compaction IAGP N RGD:5509061 20141003 MGI PMID:17620419 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0014117 increased pancreatic beta cell apoptosis IAGP N RGD:5509061 20201231 MGI PMID:31509750 1622878 Cdk8 cyclin dependent kinase 8 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20211021 MGI 1622893 Or8h8 olfactory receptor family 8 subfamily H member 8 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622895 Or12d17 olfactory receptor family 12 subfamily D member 17 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240801 MGI PMID:35108512 1622905 Garin1a golgi associated RAB2 interactor 1A gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20211209 MGI PMID:34714330 1622905 Garin1a golgi associated RAB2 interactor 1A gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1622905 Garin1a golgi associated RAB2 interactor 1A gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1622905 Garin1a golgi associated RAB2 interactor 1A gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1622905 Garin1a golgi associated RAB2 interactor 1A gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1622905 Garin1a golgi associated RAB2 interactor 1A gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 1622905 Garin1a golgi associated RAB2 interactor 1A gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20230601 MGI 1622905 Garin1a golgi associated RAB2 interactor 1A gene MP:0001262 decreased body weight IEA N RGD:5509061 20230601 MGI 1622905 Garin1a golgi associated RAB2 interactor 1A gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230601 MGI 1622905 Garin1a golgi associated RAB2 interactor 1A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20211209 MGI PMID:34714330 1622905 Garin1a golgi associated RAB2 interactor 1A gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 1622905 Garin1a golgi associated RAB2 interactor 1A gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1622905 Garin1a golgi associated RAB2 interactor 1A gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20211209 MGI PMID:34714330 1622905 Garin1a golgi associated RAB2 interactor 1A gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20211209 MGI PMID:34714330 1622905 Garin1a golgi associated RAB2 interactor 1A gene MP:0009709 hydrometra IEA N RGD:5509061 20230601 MGI 1622907 Map7d1 MAP7 domain containing 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1622907 Map7d1 MAP7 domain containing 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 1622907 Map7d1 MAP7 domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622909 Polr2h polymerase (RNA) II (DNA directed) polypeptide H gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20210128 MGI 1622909 Polr2h polymerase (RNA) II (DNA directed) polypeptide H gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1622909 Polr2h polymerase (RNA) II (DNA directed) polypeptide H gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20210520 MGI 1622909 Polr2h polymerase (RNA) II (DNA directed) polypeptide H gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20210128 MGI 1622909 Polr2h polymerase (RNA) II (DNA directed) polypeptide H gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622909 Polr2h polymerase (RNA) II (DNA directed) polypeptide H gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1622909 Polr2h polymerase (RNA) II (DNA directed) polypeptide H gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0001148 enlarged testis IEA N RGD:5509061 20210826 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20210826 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1622911 Trappc1 trafficking protein particle complex 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1622912 Fat2 FAT atypical cadherin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19966810 1622913 Ces1a carboxylesterase 1A gene MP:0003394 increased cardiac output IEA N RGD:5509061 20200402 MGI 1622915 Adgrd1 adhesion G protein-coupled receptor D1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1622915 Adgrd1 adhesion G protein-coupled receptor D1 gene MP:0001926 female infertility IEA N RGD:5509061 20160421 MGI 1622915 Adgrd1 adhesion G protein-coupled receptor D1 gene MP:0003699 abnormal female reproductive system physiology IEA N RGD:5509061 20210114 MGI 1622915 Adgrd1 adhesion G protein-coupled receptor D1 gene MP:0004794 increased anti-nuclear antigen antibody level IEA N RGD:5509061 20201022 MGI 1622915 Adgrd1 adhesion G protein-coupled receptor D1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20230601 MGI 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:22958920 1622919 Bbs12 Bardet-Biedl syndrome 12 gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:22958920 1622922 Slc7a14 solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:24670872 1622922 Slc7a14 solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 gene MP:0004397 absent cochlear inner hair cells IAGP N RGD:5509061 20220519 MGI PMID:35394837 1622922 Slc7a14 solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20220519 MGI PMID:35394837 1622922 Slc7a14 solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20220519 MGI PMID:35394837 1622922 Slc7a14 solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 gene MP:0004535 absent inner hair cell stereocilia IAGP N RGD:5509061 20220519 MGI PMID:35394837 1622922 Slc7a14 solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20220519 MGI PMID:35394837 1622922 Slc7a14 solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:24670872 1622922 Slc7a14 solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200310 MGI PMID:24670872 1622922 Slc7a14 solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20220519 MGI PMID:35394837 1622922 Slc7a14 solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200310 MGI PMID:24670872 1622922 Slc7a14 solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20220519 MGI PMID:35394837 1622922 Slc7a14 solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20220519 MGI PMID:35394837 1622923 Mcmdc2 minichromosome maintenance domain containing 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20170615 MGI PMID:27760146 1622923 Mcmdc2 minichromosome maintenance domain containing 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20170615 MGI PMID:27760146 1622923 Mcmdc2 minichromosome maintenance domain containing 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20170615 MGI PMID:27760146 1622923 Mcmdc2 minichromosome maintenance domain containing 2 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20170615 MGI PMID:27760146 1622923 Mcmdc2 minichromosome maintenance domain containing 2 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20170615 MGI PMID:27760146 1622923 Mcmdc2 minichromosome maintenance domain containing 2 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20170615 MGI PMID:27760146 1622923 Mcmdc2 minichromosome maintenance domain containing 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20170615 MGI PMID:27760146 1622923 Mcmdc2 minichromosome maintenance domain containing 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20170615 MGI PMID:27760146 1622923 Mcmdc2 minichromosome maintenance domain containing 2 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20170615 MGI PMID:27760146 1622923 Mcmdc2 minichromosome maintenance domain containing 2 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20170615 MGI PMID:27760146 1622924 Dusp5 dual specificity phosphatase 5 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20170824 MGI PMID:25398911 1622924 Dusp5 dual specificity phosphatase 5 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20170824 MGI PMID:27936095 1622924 Dusp5 dual specificity phosphatase 5 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20170824 MGI PMID:27936095 1622924 Dusp5 dual specificity phosphatase 5 gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20170824 MGI PMID:25398911 1622924 Dusp5 dual specificity phosphatase 5 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20170824 MGI PMID:25489104 1622924 Dusp5 dual specificity phosphatase 5 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20170824 MGI PMID:27936095 1622924 Dusp5 dual specificity phosphatase 5 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20170824 MGI PMID:25398911 1622924 Dusp5 dual specificity phosphatase 5 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20170824 MGI PMID:25398911 1622924 Dusp5 dual specificity phosphatase 5 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20170824 MGI PMID:27936095 1622924 Dusp5 dual specificity phosphatase 5 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20170824 MGI PMID:27936095 1622924 Dusp5 dual specificity phosphatase 5 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20170824 MGI PMID:27936095 1622924 Dusp5 dual specificity phosphatase 5 gene MP:0020184 abnormal susceptibility to parasitic infection IAGP N RGD:5509061 20170824 MGI PMID:25398911 1622925 Calhm3 calcium homeostasis modulator 3 gene MP:0001985 abnormal gustatory system physiology IAGP N RGD:5509061 20190620 MGI PMID:29681531 1622925 Calhm3 calcium homeostasis modulator 3 gene MP:0004209 abnormal sweet taste sensitivity IAGP N RGD:5509061 20190620 MGI PMID:29681531 1622925 Calhm3 calcium homeostasis modulator 3 gene MP:0004210 abnormal bitter taste sensitivity IAGP N RGD:5509061 20190620 MGI PMID:29681531 1622925 Calhm3 calcium homeostasis modulator 3 gene MP:0004212 abnormal salty taste sensitivity IAGP N RGD:5509061 20190620 MGI PMID:29681531 1622925 Calhm3 calcium homeostasis modulator 3 gene MP:0004213 abnormal umami taste sensitivity IAGP N RGD:5509061 20190620 MGI PMID:29681531 1622926 Sec31b SEC31 homolog B, COPII coat complex component gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20240523 MGI 1622926 Sec31b SEC31 homolog B, COPII coat complex component gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20220811 MGI 1622929 Wdcp WD repeat and coiled coil containing gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20240523 MGI 1622929 Wdcp WD repeat and coiled coil containing gene MP:0001785 edema IEA N RGD:5509061 20240523 MGI 1622929 Wdcp WD repeat and coiled coil containing gene MP:0001914 hemorrhage IEA N RGD:5509061 20240523 MGI 1622929 Wdcp WD repeat and coiled coil containing gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20240523 MGI 1622929 Wdcp WD repeat and coiled coil containing gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1622931 Enpp7 ectonucleotide pyrophosphatase/phosphodiesterase 7 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21177474 1622931 Enpp7 ectonucleotide pyrophosphatase/phosphodiesterase 7 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:21177474 1622931 Enpp7 ectonucleotide pyrophosphatase/phosphodiesterase 7 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:21177474 1622931 Enpp7 ectonucleotide pyrophosphatase/phosphodiesterase 7 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:21177474 1622931 Enpp7 ectonucleotide pyrophosphatase/phosphodiesterase 7 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:21177474 1622931 Enpp7 ectonucleotide pyrophosphatase/phosphodiesterase 7 gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20141003 MGI PMID:21177474 1622939 Prtg protogenin gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20211028 MGI PMID:23744351 1622939 Prtg protogenin gene MP:0000111 cleft palate IEA N RGD:5509061 20231207 MGI 1622939 Prtg protogenin gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20211028 MGI PMID:23744351 1622939 Prtg protogenin gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20211028 MGI PMID:23744351 1622939 Prtg protogenin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20211028 MGI PMID:23744351 1622939 Prtg protogenin gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20211028 MGI PMID:23744351 1622939 Prtg protogenin gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20211028 MGI PMID:23744351 1622939 Prtg protogenin gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20211028 MGI PMID:23744351 1622939 Prtg protogenin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20211028 MGI PMID:23744351 1622939 Prtg protogenin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1622939 Prtg protogenin gene MP:0012761 increased cranial neural crest cell apoptosis IAGP N RGD:5509061 20211028 MGI PMID:23744351 1622939 Prtg protogenin gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20211028 MGI PMID:23744351 1622939 Prtg protogenin gene MP:0030203 short nasal septum IAGP N RGD:5509061 20211028 MGI PMID:23744351 1622939 Prtg protogenin gene MP:0030206 thin nasal septum IAGP N RGD:5509061 20211028 MGI PMID:23744351 1622942 Cplx3 complexin 3 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:19386896 1622942 Cplx3 complexin 3 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:18505837 1622942 Cplx3 complexin 3 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:19386896 1622942 Cplx3 complexin 3 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18505837 1622942 Cplx3 complexin 3 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19386896 1622942 Cplx3 complexin 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18505837 1622942 Cplx3 complexin 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18505837 1622942 Cplx3 complexin 3 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:18505837 1622942 Cplx3 complexin 3 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19386896 1622942 Cplx3 complexin 3 gene MP:0008520 disorganized retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:19386896 1622942 Cplx3 complexin 3 gene MP:0010746 abnormal pre-Botzinger complex physiology IAGP N RGD:5509061 20141003 MGI PMID:18505837 1622942 Cplx3 complexin 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18505837 1622942 Cplx3 complexin 3 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:18505837 1622942 Cplx3 complexin 3 gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:18505837 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20211021 MGI 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:21965605 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:19503064 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:20231469 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:21965605 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20231469 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:21965605 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20231469 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19503064 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21965605 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20231469 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19503064 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0011611 abnormal circulating ghrelin level IAGP N RGD:5509061 20141003 MGI PMID:19503064 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0011613 decreased circulating ghrelin level IAGP N RGD:5509061 20141003 MGI PMID:20231469 1622944 Mboat4 membrane bound O-acyltransferase domain containing 4 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:19503064 1622946 Zbtb45 zinc finger and BTB domain containing 45 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 1622946 Zbtb45 zinc finger and BTB domain containing 45 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 1622950 Zfp418 zinc finger protein 418 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:29065170 1622950 Zfp418 zinc finger protein 418 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20200310 MGI PMID:29065170 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20190704 MGI PMID:28317850 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20190704 MGI PMID:28317850 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20210715 MGI PMID:27881734 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20210715 MGI PMID:27881734 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0003718 maternal effect IAGP N RGD:5509061 20190704 MGI PMID:28317850 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0003718 maternal effect IAGP N RGD:5509061 20210715 MGI PMID:27881734 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38786026 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20190704 MGI PMID:28317850 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20190704 MGI PMID:28317850 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20210715 MGI PMID:27881734 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20211021 MGI 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20220811 MGI 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0012128 abnormal blastocyst formation IAGP N RGD:5509061 20210715 MGI PMID:27881734 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:28317850 1622951 Nlrp2 NLR family, pyrin domain containing 2 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:28317850 1622953 Zfp628 zinc finger protein 628 gene MP:0001147 small testis IAGP N RGD:5509061 20201022 MGI PMID:31932482 1622953 Zfp628 zinc finger protein 628 gene MP:0001925 male infertility IAGP N RGD:5509061 20201022 MGI PMID:31932482 1622953 Zfp628 zinc finger protein 628 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20201022 MGI PMID:31932482 1622953 Zfp628 zinc finger protein 628 gene MP:0005159 azoospermia IAGP N RGD:5509061 20201022 MGI PMID:31932482 1622953 Zfp628 zinc finger protein 628 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20201022 MGI PMID:31932482 1622953 Zfp628 zinc finger protein 628 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20201022 MGI PMID:31932482 1622953 Zfp628 zinc finger protein 628 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1622953 Zfp628 zinc finger protein 628 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20201022 MGI PMID:31932482 1622953 Zfp628 zinc finger protein 628 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20201022 MGI PMID:31932482 1622954 Shisa7 shisa family member 7 gene MP:0000745 tremors IEA N RGD:5509061 20240523 MGI 1622954 Shisa7 shisa family member 7 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1622954 Shisa7 shisa family member 7 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 1622954 Shisa7 shisa family member 7 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 1622954 Shisa7 shisa family member 7 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20180524 MGI PMID:29199957 1622954 Shisa7 shisa family member 7 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 1622954 Shisa7 shisa family member 7 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1622954 Shisa7 shisa family member 7 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20180524 MGI PMID:29199957 1622954 Shisa7 shisa family member 7 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20180524 MGI PMID:29199957 1622954 Shisa7 shisa family member 7 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1622954 Shisa7 shisa family member 7 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20180524 MGI PMID:29199957 1622954 Shisa7 shisa family member 7 gene MP:0011272 short excitatory postsynaptic current rise time IAGP N RGD:5509061 20180524 MGI PMID:29199957 1622954 Shisa7 shisa family member 7 gene MP:0011274 short excitatory postsynaptic current decay time IAGP N RGD:5509061 20180524 MGI PMID:29199957 1622954 Shisa7 shisa family member 7 gene MP:0012319 fast extinction of fear memory IAGP N RGD:5509061 20180524 MGI PMID:29199957 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622958 Gpat3 glycerol-3-phosphate acyltransferase 3 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20160414 MGI PMID:24714397 1622960 Abitram actin binding transcription modulator gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20201022 MGI 1622960 Abitram actin binding transcription modulator gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20220519 MGI 1622960 Abitram actin binding transcription modulator gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20220519 MGI 1622960 Abitram actin binding transcription modulator gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1622960 Abitram actin binding transcription modulator gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20240523 MGI 1622961 Slc17a9 solute carrier family 17, member 9 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20180301 MGI PMID:25331291 1622961 Slc17a9 solute carrier family 17, member 9 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20170105 MGI 1622961 Slc17a9 solute carrier family 17, member 9 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20160811 MGI 1622961 Slc17a9 solute carrier family 17, member 9 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1622961 Slc17a9 solute carrier family 17, member 9 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180301 MGI PMID:25331291 1622961 Slc17a9 solute carrier family 17, member 9 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20180301 MGI PMID:25331291 1622961 Slc17a9 solute carrier family 17, member 9 gene MP:0002909 abnormal adrenal gland physiology IAGP N RGD:5509061 20180301 MGI PMID:25331291 1622961 Slc17a9 solute carrier family 17, member 9 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180301 MGI PMID:25331291 1622961 Slc17a9 solute carrier family 17, member 9 gene MP:0011479 abnormal catecholamine level IAGP N RGD:5509061 20180301 MGI PMID:25331291 1622961 Slc17a9 solute carrier family 17, member 9 gene MP:0013570 abnormal neuroendocrine gland physiology IAGP N RGD:5509061 20180301 MGI PMID:25331291 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17626060 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16015375 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150212 MGI PMID:16015375 1622962 Taf4 TATA-box binding protein associated factor 4 gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16015375 1622964 Zfp217 zinc finger protein 217 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20210826 MGI PMID:34065474 1622964 Zfp217 zinc finger protein 217 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20210826 MGI PMID:34065474 1622964 Zfp217 zinc finger protein 217 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20210826 MGI PMID:34065474 1622964 Zfp217 zinc finger protein 217 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20210826 MGI PMID:34065474 1622964 Zfp217 zinc finger protein 217 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20210826 MGI PMID:34065474 1622964 Zfp217 zinc finger protein 217 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20210826 MGI PMID:34065474 1622964 Zfp217 zinc finger protein 217 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20210826 MGI PMID:34065474 1622964 Zfp217 zinc finger protein 217 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20210826 MGI PMID:34065474 1622964 Zfp217 zinc finger protein 217 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20210826 MGI PMID:34065474 1622964 Zfp217 zinc finger protein 217 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210826 MGI PMID:34065474 1622964 Zfp217 zinc finger protein 217 gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20210826 MGI PMID:34065474 1622965 Tshz2 teashirt zinc finger family member 2 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:14645530 1622965 Tshz2 teashirt zinc finger family member 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14645530 1622965 Tshz2 teashirt zinc finger family member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1622967 Spout1 SPOUT domain containing methyltransferase 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14663139 1622967 Spout1 SPOUT domain containing methyltransferase 1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:14663139 1622967 Spout1 SPOUT domain containing methyltransferase 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:14663139 1622967 Spout1 SPOUT domain containing methyltransferase 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14663139 1622968 Gbgt1 globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20181227 MGI 1622968 Gbgt1 globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 1622968 Gbgt1 globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20181227 MGI 1622968 Gbgt1 globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20181227 MGI 1622968 Gbgt1 globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0000692 small spleen IEA N RGD:5509061 20201022 MGI 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230323 MGI PMID:36173683 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20230323 MGI PMID:36173683 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210826 MGI 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20210325 MGI PMID:33113364 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20230323 MGI PMID:36173683 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20240509 MGI PMID:32081855 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20210325 MGI PMID:33113364 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20230323 MGI PMID:36173683 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20240509 MGI PMID:32081855 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002064 seizures IAGP N RGD:5509061 20210325 MGI PMID:33113364 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002064 seizures IAGP N RGD:5509061 20230323 MGI PMID:36173683 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002064 seizures IAGP N RGD:5509061 20240509 MGI PMID:32081855 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20230323 MGI PMID:36173683 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20151119 MGI 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20210325 MGI PMID:33113364 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20230420 MGI PMID:35197318 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20170518 MGI PMID:25609627 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20230420 MGI PMID:35197318 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20170518 MGI PMID:25609627 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20230420 MGI PMID:35197318 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20240509 MGI PMID:32081855 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20210325 MGI PMID:33113364 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20240509 MGI PMID:32081855 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0002989 small kidney IEA N RGD:5509061 20201022 MGI 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0003247 abnormal glutaminergic neuron morphology IAGP N RGD:5509061 20210325 MGI PMID:33113364 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20230323 MGI PMID:36173683 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0003488 decreased channel response intensity IAGP N RGD:5509061 20170921 MGI PMID:26559620 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0003631 nervous system phenotype IAGP N RGD:5509061 20230420 MGI PMID:35197318 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20210325 MGI PMID:33113364 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20210325 MGI PMID:33113364 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20230323 MGI PMID:36173683 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20170921 MGI PMID:26559620 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210826 MGI 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20170921 MGI PMID:26559620 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20230420 MGI PMID:35197318 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0008532 decreased chemical nociceptive threshold IAGP N RGD:5509061 20170921 MGI PMID:26559620 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20210325 MGI PMID:33113364 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20210325 MGI PMID:33113364 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0010055 abnormal sensory neuron physiology IAGP N RGD:5509061 20170518 MGI PMID:25609627 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0010072 increased pruritus IAGP N RGD:5509061 20170921 MGI PMID:26559620 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20240509 MGI PMID:32081855 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20230323 MGI PMID:36173683 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0011987 abnormal GABAergic neuron physiology IAGP N RGD:5509061 20210325 MGI PMID:33113364 1622971 Kcnt1 potassium channel, subfamily T, member 1 gene MP:0020870 decreased thigmotaxis IAGP N RGD:5509061 20230420 MGI PMID:35197318 1622972 Sohlh1 spermatogenesis and oogenesis specific basic helix-loop-helix 1 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220519 MGI PMID:16690745 1622972 Sohlh1 spermatogenesis and oogenesis specific basic helix-loop-helix 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220519 MGI PMID:16564520 1622972 Sohlh1 spermatogenesis and oogenesis specific basic helix-loop-helix 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220519 MGI PMID:16564520 1622972 Sohlh1 spermatogenesis and oogenesis specific basic helix-loop-helix 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20220519 MGI PMID:16690745 1622972 Sohlh1 spermatogenesis and oogenesis specific basic helix-loop-helix 1 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20220519 MGI PMID:16690745 1622972 Sohlh1 spermatogenesis and oogenesis specific basic helix-loop-helix 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16564520 1622972 Sohlh1 spermatogenesis and oogenesis specific basic helix-loop-helix 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20220519 MGI PMID:16690745 1622972 Sohlh1 spermatogenesis and oogenesis specific basic helix-loop-helix 1 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20220519 MGI PMID:16690745 1622972 Sohlh1 spermatogenesis and oogenesis specific basic helix-loop-helix 1 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20220519 MGI PMID:16690745 1622972 Sohlh1 spermatogenesis and oogenesis specific basic helix-loop-helix 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16564520 1622972 Sohlh1 spermatogenesis and oogenesis specific basic helix-loop-helix 1 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20220519 MGI PMID:16690745 1622972 Sohlh1 spermatogenesis and oogenesis specific basic helix-loop-helix 1 gene MP:0011126 absent primary ovarian follicles IAGP N RGD:5509061 20220519 MGI PMID:16690745 1622974 Obp2a odorant binding protein 2A gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160421 MGI 1622974 Obp2a odorant binding protein 2A gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1622975 Man1b1 mannosidase, alpha, class 1B, member 1 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20221215 MGI 1622975 Man1b1 mannosidase, alpha, class 1B, member 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1622976 Tbpl2 TATA box binding protein like 2 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19759265 1622976 Tbpl2 TATA box binding protein like 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:19759265 1622976 Tbpl2 TATA box binding protein like 2 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:19759265 1622976 Tbpl2 TATA box binding protein like 2 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20200130 MGI PMID:19759265 1622976 Tbpl2 TATA box binding protein like 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19759265 1622976 Tbpl2 TATA box binding protein like 2 gene MP:0003697 absent zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:19759265 1622976 Tbpl2 TATA box binding protein like 2 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:19759265 1622976 Tbpl2 TATA box binding protein like 2 gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:19759265 1622976 Tbpl2 TATA box binding protein like 2 gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20141003 MGI PMID:19759265 1622976 Tbpl2 TATA box binding protein like 2 gene MP:0011120 increased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:19759265 1622976 Tbpl2 TATA box binding protein like 2 gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:19759265 1622976 Tbpl2 TATA box binding protein like 2 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20200130 MGI PMID:19759265 1622976 Tbpl2 TATA box binding protein like 2 gene MP:0031015 abnormal granulosa cell apoptosis IAGP N RGD:5509061 20200130 MGI PMID:19759265 1622976 Tbpl2 TATA box binding protein like 2 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:19759265 1622976 Tbpl2 TATA box binding protein like 2 gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220630 MGI PMID:19759265 1622977 C1ql2 complement component 1, q subcomponent-like 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 1622977 C1ql2 complement component 1, q subcomponent-like 2 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1622977 C1ql2 complement component 1, q subcomponent-like 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 1622977 C1ql2 complement component 1, q subcomponent-like 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20201022 MGI 1622979 Npbwr1 neuropeptides B/W receptor 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:12925742 1622979 Npbwr1 neuropeptides B/W receptor 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12925742 1622979 Npbwr1 neuropeptides B/W receptor 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:12925742 1622979 Npbwr1 neuropeptides B/W receptor 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:12925742 1622979 Npbwr1 neuropeptides B/W receptor 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12925742 1622979 Npbwr1 neuropeptides B/W receptor 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12925742 1622979 Npbwr1 neuropeptides B/W receptor 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12925742 1622979 Npbwr1 neuropeptides B/W receptor 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12925742 1622979 Npbwr1 neuropeptides B/W receptor 1 gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:12925742 1622979 Npbwr1 neuropeptides B/W receptor 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:12925742 1622979 Npbwr1 neuropeptides B/W receptor 1 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:12925742 1622979 Npbwr1 neuropeptides B/W receptor 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12925742 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22172515 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0009122 decreased white fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:20674860 1622981 Lclat1 lysocardiolipin acyltransferase 1 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:20674860 1622982 Adm2 adrenomedullin 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1622982 Adm2 adrenomedullin 2 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20181227 MGI 1622982 Adm2 adrenomedullin 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20181227 MGI 1622982 Adm2 adrenomedullin 2 gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 1622982 Adm2 adrenomedullin 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200102 MGI PMID:29980671 1622982 Adm2 adrenomedullin 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20200102 MGI PMID:29980671 1622982 Adm2 adrenomedullin 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200102 MGI PMID:29980671 1622982 Adm2 adrenomedullin 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200102 MGI PMID:29980671 1622982 Adm2 adrenomedullin 2 gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20200102 MGI PMID:29980671 1622982 Adm2 adrenomedullin 2 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20200102 MGI PMID:29980671 1622982 Adm2 adrenomedullin 2 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20200102 MGI PMID:29980671 1622982 Adm2 adrenomedullin 2 gene MP:0008725 increased heart atrium size IEA N RGD:5509061 20181227 MGI 1622982 Adm2 adrenomedullin 2 gene MP:0011350 abnormal proximal convoluted tubule brush border morphology IAGP N RGD:5509061 20200102 MGI PMID:29980671 1622982 Adm2 adrenomedullin 2 gene MP:0011824 increased cell chemotaxis IAGP N RGD:5509061 20200102 MGI PMID:29980671 1622982 Adm2 adrenomedullin 2 gene MP:0013022 increased Ly6C high monocyte number IAGP N RGD:5509061 20200102 MGI PMID:29980671 1622982 Adm2 adrenomedullin 2 gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20200102 MGI PMID:29980671 1622983 Alg12 ALG12 alpha-1,6-mannosyltransferase gene MP:0000745 tremors IEA N RGD:5509061 20240523 MGI 1622984 Zbed4 zinc finger, BED type containing 4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20231207 MGI 1622984 Zbed4 zinc finger, BED type containing 4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20231207 MGI 1622984 Zbed4 zinc finger, BED type containing 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20231207 MGI 1622984 Zbed4 zinc finger, BED type containing 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20231207 MGI 1622984 Zbed4 zinc finger, BED type containing 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 1622984 Zbed4 zinc finger, BED type containing 4 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20231207 MGI 1622984 Zbed4 zinc finger, BED type containing 4 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20231207 MGI 1622984 Zbed4 zinc finger, BED type containing 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1622985 Brd1 bromodomain containing 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0011246 abnormal fetal liver hematopoietic progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622985 Brd1 bromodomain containing 1 gene MP:0012243 decreased hepatoblast number IAGP N RGD:5509061 20141003 MGI PMID:21753189 1622987 Rtl6 retrotransposon Gag like 6 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20221124 MGI PMID:36162816 1622987 Rtl6 retrotransposon Gag like 6 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20221124 MGI PMID:36162816 1622991 Atxn7l3 ataxin 7-like 3 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201231 MGI 1622991 Atxn7l3 ataxin 7-like 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210826 MGI 1622991 Atxn7l3 ataxin 7-like 3 gene MP:0002764 short tibia IEA N RGD:5509061 20200310 MGI 1622991 Atxn7l3 ataxin 7-like 3 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20200310 MGI 1622991 Atxn7l3 ataxin 7-like 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:25228644 1622991 Atxn7l3 ataxin 7-like 3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20200310 MGI 1622991 Atxn7l3 ataxin 7-like 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622991 Atxn7l3 ataxin 7-like 3 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20200310 MGI 1622993 Rundc1 RUN domain containing 1 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20200310 MGI 1622993 Rundc1 RUN domain containing 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1622993 Rundc1 RUN domain containing 1 gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20200310 MGI 1622993 Rundc1 RUN domain containing 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200310 MGI 1622993 Rundc1 RUN domain containing 1 gene MP:0002947 increased hemangioma incidence IEA N RGD:5509061 20210930 MGI 1622993 Rundc1 RUN domain containing 1 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20200310 MGI 1622993 Rundc1 RUN domain containing 1 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20200310 MGI 1622993 Rundc1 RUN domain containing 1 gene MP:0006221 optic nerve hypoplasia IEA N RGD:5509061 20200310 MGI 1622993 Rundc1 RUN domain containing 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622993 Rundc1 RUN domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1622994 Mcu mitochondrial calcium uniporter gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20160721 MGI PMID:26119742 1622994 Mcu mitochondrial calcium uniporter gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24212091 1622994 Mcu mitochondrial calcium uniporter gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24212091 1622994 Mcu mitochondrial calcium uniporter gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 1622994 Mcu mitochondrial calcium uniporter gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20160721 MGI PMID:26119742 1622994 Mcu mitochondrial calcium uniporter gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20160721 MGI PMID:26119742 1622994 Mcu mitochondrial calcium uniporter gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20160721 MGI PMID:26119742 1622994 Mcu mitochondrial calcium uniporter gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 1622994 Mcu mitochondrial calcium uniporter gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20160721 MGI PMID:26119742 1622994 Mcu mitochondrial calcium uniporter gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1622994 Mcu mitochondrial calcium uniporter gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20160721 MGI PMID:26119742 1622994 Mcu mitochondrial calcium uniporter gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20171116 MGI PMID:27184846 1622994 Mcu mitochondrial calcium uniporter gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20200402 MGI PMID:31501572 1622994 Mcu mitochondrial calcium uniporter gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20201001 MGI PMID:24212091 1622994 Mcu mitochondrial calcium uniporter gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 1622994 Mcu mitochondrial calcium uniporter gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:24212091 1622994 Mcu mitochondrial calcium uniporter gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 1622994 Mcu mitochondrial calcium uniporter gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1622994 Mcu mitochondrial calcium uniporter gene MP:0011134 decreased lung endothelial cell migration IAGP N RGD:5509061 20171116 MGI PMID:27184846 1622994 Mcu mitochondrial calcium uniporter gene MP:0011140 decreased lung endothelial cell proliferation IAGP N RGD:5509061 20171116 MGI PMID:27184846 1622994 Mcu mitochondrial calcium uniporter gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:24212091 1622994 Mcu mitochondrial calcium uniporter gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 1622994 Mcu mitochondrial calcium uniporter gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20201001 MGI PMID:24212091 1622996 Afg1l AFG1 like ATPase gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20230601 MGI 1622996 Afg1l AFG1 like ATPase gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1622996 Afg1l AFG1 like ATPase gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20230601 MGI 1622996 Afg1l AFG1 like ATPase gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 1622996 Afg1l AFG1 like ATPase gene MP:0005542 cornea vascularization IEA N RGD:5509061 20240627 MGI 1623001 Afg2b AFG2 AAA ATPase homolog B gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1623001 Afg2b AFG2 AAA ATPase homolog B gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241017 MGI 1623001 Afg2b AFG2 AAA ATPase homolog B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1623001 Afg2b AFG2 AAA ATPase homolog B gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241017 MGI 1623003 Slc10a3 solute carrier family 10 (sodium/bile acid cotransporter family), member 3 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 1623003 Slc10a3 solute carrier family 10 (sodium/bile acid cotransporter family), member 3 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 1623003 Slc10a3 solute carrier family 10 (sodium/bile acid cotransporter family), member 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220519 MGI 1623004 Depp1 DEPP1 autophagy regulator gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15977181 1623005 Prdm9 PR domain containing 9 gene MP:0001127 small ovary IAGP N RGD:5509061 20210121 MGI PMID:33097538 1623005 Prdm9 PR domain containing 9 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20200310 MGI PMID:16292313 1623005 Prdm9 PR domain containing 9 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:22258617 1623005 Prdm9 PR domain containing 9 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20210121 MGI PMID:33097538 1623005 Prdm9 PR domain containing 9 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:16292313 1623005 Prdm9 PR domain containing 9 gene MP:0001925 male infertility IAGP N RGD:5509061 20210121 MGI PMID:33097538 1623005 Prdm9 PR domain containing 9 gene MP:0001925 male infertility IAGP N RGD:5509061 20211223 MGI PMID:32744506 1623005 Prdm9 PR domain containing 9 gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:16292313 1623005 Prdm9 PR domain containing 9 gene MP:0001926 female infertility IAGP N RGD:5509061 20210121 MGI PMID:33097538 1623005 Prdm9 PR domain containing 9 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20200310 MGI PMID:16292313 1623005 Prdm9 PR domain containing 9 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20200310 MGI PMID:25568937 1623005 Prdm9 PR domain containing 9 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20200310 MGI PMID:22258617 1623005 Prdm9 PR domain containing 9 gene MP:0002208 abnormal germ cell morphology IAGP N RGD:5509061 20200310 MGI PMID:22258617 1623005 Prdm9 PR domain containing 9 gene MP:0002216 abnormal seminiferous tubule morphology IEA N RGD:5509061 20200310 MGI 1623005 Prdm9 PR domain containing 9 gene MP:0002777 absent ovarian follicles IEA N RGD:5509061 20200310 MGI 1623005 Prdm9 PR domain containing 9 gene MP:0004244 abnormal miscarriage rate IAGP N RGD:5509061 20210204 MGI PMID:33097538 1623005 Prdm9 PR domain containing 9 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:16292313 1623005 Prdm9 PR domain containing 9 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:22258617 1623005 Prdm9 PR domain containing 9 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210204 MGI PMID:33097538 1623005 Prdm9 PR domain containing 9 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200310 MGI PMID:22258617 1623005 Prdm9 PR domain containing 9 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:16292313 1623005 Prdm9 PR domain containing 9 gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:22258617 1623005 Prdm9 PR domain containing 9 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20200310 MGI PMID:16292313 1623005 Prdm9 PR domain containing 9 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20210121 MGI PMID:33097538 1623005 Prdm9 PR domain containing 9 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20210304 MGI PMID:30853435 1623005 Prdm9 PR domain containing 9 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20200310 MGI PMID:16292313 1623005 Prdm9 PR domain containing 9 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20210121 MGI PMID:33097538 1623005 Prdm9 PR domain containing 9 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20200310 MGI PMID:22258617 1623005 Prdm9 PR domain containing 9 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20200310 MGI PMID:16292313 1623005 Prdm9 PR domain containing 9 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20210121 MGI PMID:33097538 1623005 Prdm9 PR domain containing 9 gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20210121 MGI PMID:33097538 1623005 Prdm9 PR domain containing 9 gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20210121 MGI PMID:33097538 1623005 Prdm9 PR domain containing 9 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20200310 MGI PMID:16292313 1623005 Prdm9 PR domain containing 9 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20210121 MGI PMID:33097538 1623005 Prdm9 PR domain containing 9 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20211223 MGI PMID:32744506 1623005 Prdm9 PR domain containing 9 gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20210204 MGI PMID:33097538 1623005 Prdm9 PR domain containing 9 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20200310 MGI PMID:16292313 1623005 Prdm9 PR domain containing 9 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20210304 MGI PMID:30853435 1623005 Prdm9 PR domain containing 9 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20211223 MGI PMID:32744506 1623006 Fbxl21 F-box and leucine-rich repeat protein 21 gene MP:0001513 limb grasping IEA N RGD:5509061 20181227 MGI 1623006 Fbxl21 F-box and leucine-rich repeat protein 21 gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20171012 MGI PMID:23452855 1623006 Fbxl21 F-box and leucine-rich repeat protein 21 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20171012 MGI PMID:23452855 1623006 Fbxl21 F-box and leucine-rich repeat protein 21 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:23452856 1623006 Fbxl21 F-box and leucine-rich repeat protein 21 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:23452855 1623007 Tmem60 transmembrane protein 60 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1623007 Tmem60 transmembrane protein 60 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1623007 Tmem60 transmembrane protein 60 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1623007 Tmem60 transmembrane protein 60 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1623007 Tmem60 transmembrane protein 60 gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20220519 MGI 1623007 Tmem60 transmembrane protein 60 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220811 MGI 1623007 Tmem60 transmembrane protein 60 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210520 MGI 1623007 Tmem60 transmembrane protein 60 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20200514 MGI 1623007 Tmem60 transmembrane protein 60 gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20240523 MGI 1623007 Tmem60 transmembrane protein 60 gene MP:0013771 decreased effector memory T-helper cell number IEA N RGD:5509061 20211021 MGI 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21195350 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23078342 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23078342 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20220519 MGI 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23011063 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23078342 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21195350 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20220811 MGI 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:23078342 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21195350 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:23078342 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:23078342 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21195350 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:23078342 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21195350 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23011063 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23078342 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21195350 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23011063 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23078342 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23011063 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23011063 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20151217 MGI PMID:23078342 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220811 MGI 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23011063 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23011063 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0009300 increased parametrial fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23011063 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23011063 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20160421 MGI PMID:23078342 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:21195350 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:23011063 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:23078342 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:23011063 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:23078342 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:21195350 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0030022 decreased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:21195350 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:23011063 1623009 Tbc1d4 TBC1 domain family, member 4 gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:23078342 1623011 Themis thymocyte selection associated gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19597499 1623011 Themis thymocyte selection associated gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19805304 1623011 Themis thymocyte selection associated gene MP:0001606 impaired hematopoiesis IEA N RGD:5509061 20161201 MGI 1623011 Themis thymocyte selection associated gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19597497 1623011 Themis thymocyte selection associated gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19597498 1623011 Themis thymocyte selection associated gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19620281 1623011 Themis thymocyte selection associated gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19805304 1623011 Themis thymocyte selection associated gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:19597499 1623011 Themis thymocyte selection associated gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IEA N RGD:5509061 20180215 MGI 1623011 Themis thymocyte selection associated gene MP:0002619 abnormal lymphocyte morphology IEA N RGD:5509061 20141003 MGI 1623011 Themis thymocyte selection associated gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:19597498 1623011 Themis thymocyte selection associated gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:19597499 1623011 Themis thymocyte selection associated gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:19597498 1623011 Themis thymocyte selection associated gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:19597499 1623011 Themis thymocyte selection associated gene MP:0004941 abnormal regulatory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19597499 1623011 Themis thymocyte selection associated gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597497 1623011 Themis thymocyte selection associated gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597498 1623011 Themis thymocyte selection associated gene MP:0005018 decreased T cell number IEA N RGD:5509061 20161201 MGI 1623011 Themis thymocyte selection associated gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597497 1623011 Themis thymocyte selection associated gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597498 1623011 Themis thymocyte selection associated gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597499 1623011 Themis thymocyte selection associated gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19597499 1623011 Themis thymocyte selection associated gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19805304 1623011 Themis thymocyte selection associated gene MP:0008039 increased NK T cell number IEA N RGD:5509061 20190530 MGI 1623011 Themis thymocyte selection associated gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597498 1623011 Themis thymocyte selection associated gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19805304 1623011 Themis thymocyte selection associated gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597497 1623011 Themis thymocyte selection associated gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597498 1623011 Themis thymocyte selection associated gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597499 1623011 Themis thymocyte selection associated gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19620281 1623011 Themis thymocyte selection associated gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19805304 1623011 Themis thymocyte selection associated gene MP:0008076 abnormal CD4-positive T cell differentiation IEA N RGD:5509061 20190530 MGI 1623011 Themis thymocyte selection associated gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20161201 MGI 1623011 Themis thymocyte selection associated gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597497 1623011 Themis thymocyte selection associated gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597498 1623011 Themis thymocyte selection associated gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597499 1623011 Themis thymocyte selection associated gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19620281 1623011 Themis thymocyte selection associated gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19805304 1623011 Themis thymocyte selection associated gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19597498 1623011 Themis thymocyte selection associated gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597497 1623011 Themis thymocyte selection associated gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19597498 1623011 Themis thymocyte selection associated gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19620281 1623011 Themis thymocyte selection associated gene MP:0008168 decreased B-1a cell number IEA N RGD:5509061 20141003 MGI 1623011 Themis thymocyte selection associated gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:19805304 1623011 Themis thymocyte selection associated gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20180215 MGI 1623011 Themis thymocyte selection associated gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20180215 MGI 1623011 Themis thymocyte selection associated gene MP:0010833 abnormal memory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19597499 1623011 Themis thymocyte selection associated gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20180215 MGI 1623011 Themis thymocyte selection associated gene MP:0010839 decreased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20180215 MGI 1623011 Themis thymocyte selection associated gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1623011 Themis thymocyte selection associated gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20161201 MGI 1623011 Themis thymocyte selection associated gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1623011 Themis thymocyte selection associated gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190530 MGI 1623011 Themis thymocyte selection associated gene MP:0012765 decreased alpha-beta T cell number IEA N RGD:5509061 20190530 MGI 1623011 Themis thymocyte selection associated gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 1623011 Themis thymocyte selection associated gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:19620281 1623011 Themis thymocyte selection associated gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20141003 MGI 1623012 Gab3 growth factor receptor bound protein 2-associated protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12640125 1623012 Gab3 growth factor receptor bound protein 2-associated protein 3 gene MP:0004514 dystocia IAGP N RGD:5509061 20200813 MGI PMID:31375526 1623012 Gab3 growth factor receptor bound protein 2-associated protein 3 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20200813 MGI PMID:31375526 1623012 Gab3 growth factor receptor bound protein 2-associated protein 3 gene MP:0008054 abnormal uterine NK cell morphology IAGP N RGD:5509061 20200813 MGI PMID:31375526 1623012 Gab3 growth factor receptor bound protein 2-associated protein 3 gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20200813 MGI PMID:31375526 1623012 Gab3 growth factor receptor bound protein 2-associated protein 3 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20200813 MGI PMID:31375526 1623012 Gab3 growth factor receptor bound protein 2-associated protein 3 gene MP:0013700 abnormal mature NK cell morphology IAGP N RGD:5509061 20200813 MGI PMID:31375526 1623017 Tmem132b transmembrane protein 132B gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20200514 MGI 1623017 Tmem132b transmembrane protein 132B gene MP:0001260 increased body weight IEA N RGD:5509061 20210128 MGI 1623017 Tmem132b transmembrane protein 132B gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1623017 Tmem132b transmembrane protein 132B gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 1623017 Tmem132b transmembrane protein 132B gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20201022 MGI 1623017 Tmem132b transmembrane protein 132B gene MP:0010896 decreased lung compliance IEA N RGD:5509061 20240523 MGI 1623018 Dhx37 DEAH-box helicase 37 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1623018 Dhx37 DEAH-box helicase 37 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240919 MGI 1623018 Dhx37 DEAH-box helicase 37 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1623018 Dhx37 DEAH-box helicase 37 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20240919 MGI 1623018 Dhx37 DEAH-box helicase 37 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1623018 Dhx37 DEAH-box helicase 37 gene MP:0012058 abnormal morula morphology IEA N RGD:5509061 20240919 MGI 1623018 Dhx37 DEAH-box helicase 37 gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20240919 MGI 1623018 Dhx37 DEAH-box helicase 37 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 1623020 Mlxip MLX interacting protein gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20181220 MGI PMID:25145386 1623020 Mlxip MLX interacting protein gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20181220 MGI PMID:25145386 1623020 Mlxip MLX interacting protein gene MP:0012107 enhanced exercise endurance IAGP N RGD:5509061 20181220 MGI PMID:25145386 1623020 Mlxip MLX interacting protein gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20181220 MGI PMID:25145386 1623020 Mlxip MLX interacting protein gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20181220 MGI PMID:25145386 1623020 Mlxip MLX interacting protein gene MP:0030673 increased circulating alanine level IAGP N RGD:5509061 20181220 MGI PMID:25145386 1623021 Plxnb3 plexin B3 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201022 MGI 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12805295 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12843301 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0000745 tremors IAGP N RGD:5509061 20151015 MGI PMID:25524707 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:21750683 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21750683 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:12805295 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:12843301 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:21750683 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:12843301 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20151015 MGI PMID:25524707 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:12805295 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20151015 MGI PMID:25524707 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:12843301 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21750683 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21750683 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20151015 MGI PMID:25524707 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20151015 MGI PMID:25524707 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:12805295 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:21750683 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12805295 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12843301 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21750683 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20151015 MGI PMID:25524707 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12805295 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12843301 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:12805295 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:21750683 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:21750683 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:12805295 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:12843301 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20151015 MGI PMID:25524707 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21750683 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20151015 MGI PMID:25524707 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20151015 MGI PMID:25524707 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:21750683 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21750683 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:21750683 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20151015 MGI PMID:25524707 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0009978 abnormal cerebellum white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:21750683 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:21750683 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0010205 abnormal oligodendrocyte apoptosis IAGP N RGD:5509061 20151015 MGI PMID:25524707 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20151015 MGI PMID:25524707 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0030987 spinal cord inflammation IAGP N RGD:5509061 20191128 MGI PMID:25524707 1623025 Gjc2 gap junction protein, gamma 2 gene MP:0030991 optic nerve inflammation IAGP N RGD:5509061 20191128 MGI PMID:25524707 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23200864 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:23200864 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20190516 MGI PMID:30808755 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0000860 abnormal primary somatosensory cortex morphology IAGP N RGD:5509061 20190516 MGI PMID:30808755 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0001258 decreased body length IAGP N RGD:5509061 20190516 MGI PMID:30808755 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23200864 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190516 MGI PMID:30808755 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23200864 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20220811 MGI 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0001307 fused cornea and lens IEA N RGD:5509061 20220811 MGI 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20220811 MGI 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20220811 MGI 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0001443 poor grooming IAGP N RGD:5509061 20190516 MGI PMID:30808755 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20190516 MGI PMID:30808755 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221215 MGI 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20190516 MGI PMID:30808755 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:23200864 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:23200864 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20221215 MGI 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0004038 lymphangiectasis IAGP N RGD:5509061 20141003 MGI PMID:23200864 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0004222 iris synechia IEA N RGD:5509061 20220811 MGI 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20190516 MGI PMID:30808755 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23200864 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20190516 MGI PMID:30808755 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0006188 calcified retina IAGP N RGD:5509061 20141003 MGI PMID:23200864 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20220811 MGI 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:23200864 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20190516 MGI PMID:30808755 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:23200864 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20190516 MGI PMID:30808755 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23200864 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20190516 MGI PMID:30808755 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23200864 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20190516 MGI PMID:30808755 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20220811 MGI 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20141003 MGI PMID:23200864 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20190516 MGI PMID:30808755 1623028 Ube3b ubiquitin protein ligase E3B gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20190516 MGI PMID:30808755 1623030 Clic1 chloride intracellular channel 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:20049953 1623030 Clic1 chloride intracellular channel 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:20049953 1623030 Clic1 chloride intracellular channel 1 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:20049953 1623030 Clic1 chloride intracellular channel 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:20049953 1623032 Dlx1as distal-less homeobox 1, antisense gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:23415800 1623032 Dlx1as distal-less homeobox 1, antisense gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23415800 1623037 Prr9 proline rich 9 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1623037 Prr9 proline rich 9 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20220519 MGI 1623038 Cstf2 cleavage stimulation factor, 3' pre-RNA subunit 2 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20160728 MGI PMID:25460602 1623038 Cstf2 cleavage stimulation factor, 3' pre-RNA subunit 2 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20160728 MGI PMID:25460602 1623038 Cstf2 cleavage stimulation factor, 3' pre-RNA subunit 2 gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20160728 MGI PMID:25460602 1623038 Cstf2 cleavage stimulation factor, 3' pre-RNA subunit 2 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20160728 MGI PMID:25460602 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20201022 MGI 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20180830 MGI PMID:21745337 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17677002 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17677002 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180830 MGI PMID:21745337 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17677002 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20141003 MGI PMID:17677002 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:17677002 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0002064 seizures IAGP N RGD:5509061 20180830 MGI PMID:21745337 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17677002 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170504 MGI 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0002928 abnormal bile duct morphology IEA N RGD:5509061 20170504 MGI 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:17677002 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0003216 absence seizures IAGP N RGD:5509061 20180830 MGI PMID:21745337 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:17677002 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20180830 MGI PMID:21745337 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0004201 fetal growth retardation IEA N RGD:5509061 20170504 MGI 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20180830 MGI PMID:21745337 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:17677002 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20180830 MGI PMID:21745337 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180830 MGI PMID:21745337 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17677002 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0011683 dual inferior vena cava IEA N RGD:5509061 20170504 MGI 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0012348 decreased susceptibility to induction of seizure by inducing agent IAGP N RGD:5509061 20180830 MGI PMID:23209433 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0012349 increased susceptibility to induction of seizure by inducing agent IAGP N RGD:5509061 20180830 MGI PMID:23209433 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0012349 increased susceptibility to induction of seizure by inducing agent IAGP N RGD:5509061 20180830 MGI PMID:7806216 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20170504 MGI 1623039 Celf4 CUGBP, Elav-like family member 4 gene MP:0014004 absent basilar artery segment IEA N RGD:5509061 20170504 MGI 1623040 Cenpf centromere protein F gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190425 MGI PMID:30856164 1623040 Cenpf centromere protein F gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170824 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0003057 abnormal epicardium morphology IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623040 Cenpf centromere protein F gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22563055 1623042 Stap2 signal transducing adaptor family member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12540842 1623043 Ttbk1 tau tubulin kinase 1 gene MP:0000745 tremors IEA N RGD:5509061 20240523 MGI 1623043 Ttbk1 tau tubulin kinase 1 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20240523 MGI 1623043 Ttbk1 tau tubulin kinase 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1623043 Ttbk1 tau tubulin kinase 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240627 MGI 1623043 Ttbk1 tau tubulin kinase 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 1623043 Ttbk1 tau tubulin kinase 1 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20240523 MGI 1623043 Ttbk1 tau tubulin kinase 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20240523 MGI 1623043 Ttbk1 tau tubulin kinase 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 1623043 Ttbk1 tau tubulin kinase 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20240523 MGI 1623043 Ttbk1 tau tubulin kinase 1 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1623043 Ttbk1 tau tubulin kinase 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20240523 MGI 1623043 Ttbk1 tau tubulin kinase 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 1623043 Ttbk1 tau tubulin kinase 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1623044 Catsperd cation channel sperm associated auxiliary subunit delta gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:21224844 1623044 Catsperd cation channel sperm associated auxiliary subunit delta gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21224844 1623044 Catsperd cation channel sperm associated auxiliary subunit delta gene MP:0002208 abnormal germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21224844 1623044 Catsperd cation channel sperm associated auxiliary subunit delta gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21224844 1623044 Catsperd cation channel sperm associated auxiliary subunit delta gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21224844 1623044 Catsperd cation channel sperm associated auxiliary subunit delta gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20141003 MGI PMID:21224844 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20210520 MGI 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:23112346 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23112346 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23112346 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:23112346 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:23112346 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:23112346 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23112346 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0004952 increased spleen weight IEA N RGD:5509061 20201022 MGI 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:23112346 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0005573 increased pulmonary respiratory rate IEA N RGD:5509061 20201022 MGI 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:23112346 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23112346 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20141003 MGI PMID:23112346 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:23112346 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0011746 spleen fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23112346 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0011747 myelofibrosis IAGP N RGD:5509061 20141003 MGI PMID:23112346 1623045 Mpig6b megakaryocyte and platelet inhibitory receptor G6b gene MP:0012125 decreased bronchoconstrictive response IEA N RGD:5509061 20201022 MGI 1623048 Fam149b family with sequence similarity 149, member B gene MP:0001925 male infertility IEA N RGD:5509061 20231207 MGI 1623050 Gldc glycine decarboxylase gene MP:0000087 absent mandible IEA N RGD:5509061 20170209 MGI 1623050 Gldc glycine decarboxylase gene MP:0000111 cleft palate IEA N RGD:5509061 20170209 MGI 1623050 Gldc glycine decarboxylase gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170209 MGI 1623050 Gldc glycine decarboxylase gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20171123 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0000440 domed cranium IAGP N RGD:5509061 20160519 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0000445 short snout IEA N RGD:5509061 20170209 MGI 1623050 Gldc glycine decarboxylase gene MP:0000519 hydronephrosis IEA N RGD:5509061 20170209 MGI 1623050 Gldc glycine decarboxylase gene MP:0000914 exencephaly IAGP N RGD:5509061 20160519 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20160519 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0000929 open neural tube IAGP N RGD:5509061 20160519 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0001293 anophthalmia IEA N RGD:5509061 20170209 MGI 1623050 Gldc glycine decarboxylase gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20160519 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20160519 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0002083 premature death IAGP N RGD:5509061 20160519 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20160519 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20210318 MGI PMID:33569080 1623050 Gldc glycine decarboxylase gene MP:0003052 omphalocele IEA N RGD:5509061 20170209 MGI 1623050 Gldc glycine decarboxylase gene MP:0003675 kidney cyst IEA N RGD:5509061 20170209 MGI 1623050 Gldc glycine decarboxylase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160519 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20160519 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20201231 MGI 1623050 Gldc glycine decarboxylase gene MP:0005170 cleft upper lip IEA N RGD:5509061 20170209 MGI 1623050 Gldc glycine decarboxylase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20160519 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20170209 MGI 1623050 Gldc glycine decarboxylase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160519 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623050 Gldc glycine decarboxylase gene MP:0011230 abnormal folic acid level IAGP N RGD:5509061 20160519 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20160519 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0030616 hyperglycinuria IAGP N RGD:5509061 20210318 MGI PMID:25736695 1623050 Gldc glycine decarboxylase gene MP:0030655 increased circulating glycine level IAGP N RGD:5509061 20210318 MGI PMID:25736695 1623051 Etv5 ets variant 5 gene MP:0000413 polyphalangy IAGP N RGD:5509061 20141003 MGI PMID:19386269 1623051 Etv5 ets variant 5 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:19898483 1623051 Etv5 ets variant 5 gene MP:0000524 decreased renal tubule number IAGP N RGD:5509061 20141003 MGI PMID:19898483 1623051 Etv5 ets variant 5 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19386269 1623051 Etv5 ets variant 5 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:24204802 1623051 Etv5 ets variant 5 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16107850 1623051 Etv5 ets variant 5 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:24204802 1623051 Etv5 ets variant 5 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16107850 1623051 Etv5 ets variant 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18032421 1623051 Etv5 ets variant 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24204802 1623051 Etv5 ets variant 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16107850 1623051 Etv5 ets variant 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18032421 1623051 Etv5 ets variant 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:24204802 1623051 Etv5 ets variant 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:24204802 1623051 Etv5 ets variant 5 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19898483 1623051 Etv5 ets variant 5 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:24204802 1623051 Etv5 ets variant 5 gene MP:0002243 abnormal vomeronasal organ morphology IAGP N RGD:5509061 20141003 MGI PMID:18032421 1623051 Etv5 ets variant 5 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:18032421 1623051 Etv5 ets variant 5 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18032421 1623051 Etv5 ets variant 5 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20141003 MGI PMID:16107850 1623051 Etv5 ets variant 5 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18032421 1623051 Etv5 ets variant 5 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19898483 1623051 Etv5 ets variant 5 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:19898483 1623051 Etv5 ets variant 5 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:19898483 1623051 Etv5 ets variant 5 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:19898483 1623051 Etv5 ets variant 5 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:19898483 1623051 Etv5 ets variant 5 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20141003 MGI PMID:18032421 1623051 Etv5 ets variant 5 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:19898483 1623051 Etv5 ets variant 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18032421 1623051 Etv5 ets variant 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:24204802 1623051 Etv5 ets variant 5 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:24204802 1623051 Etv5 ets variant 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:16107850 1623051 Etv5 ets variant 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:24204802 1623051 Etv5 ets variant 5 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:19386269 1623051 Etv5 ets variant 5 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:16107850 1623051 Etv5 ets variant 5 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:18032421 1623051 Etv5 ets variant 5 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16107850 1623051 Etv5 ets variant 5 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19386269 1623051 Etv5 ets variant 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24204802 1623051 Etv5 ets variant 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19386269 1623051 Etv5 ets variant 5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19898483 1623051 Etv5 ets variant 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19386269 1623051 Etv5 ets variant 5 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24204802 1623051 Etv5 ets variant 5 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:18032421 1623053 Airn antisense Igf2r RNA gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11845212 1623053 Airn antisense Igf2r RNA gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:22396659 1623053 Airn antisense Igf2r RNA gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:11845212 1623053 Airn antisense Igf2r RNA gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:11845212 1623053 Airn antisense Igf2r RNA gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:22396659 1623053 Airn antisense Igf2r RNA gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:22396659 1623056 Wtip WT1 interacting protein gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20221222 MGI PMID:35862649 1623056 Wtip WT1 interacting protein gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20221222 MGI PMID:35862649 1623056 Wtip WT1 interacting protein gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20221222 MGI PMID:35862649 1623056 Wtip WT1 interacting protein gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20221222 MGI PMID:35862649 1623056 Wtip WT1 interacting protein gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210805 MGI 1623057 Rusc2 RUN and SH3 domain containing 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 1623059 Eeig1 estrogen-induced osteoclastogenesis regulator 1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210415 MGI PMID:32741026 1623060 Smarca5 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5 gene MP:0000421 mottled coat IAGP N RGD:5509061 20141003 MGI PMID:15890782 1623060 Smarca5 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:14617767 1623060 Smarca5 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:14617767 1623060 Smarca5 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:14617767 1623060 Smarca5 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14617767 1623060 Smarca5 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14617767 1623060 Smarca5 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15890782 1623060 Smarca5 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:14617767 1623060 Smarca5 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5 gene MP:0012119 increased trophectoderm apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14617767 1623060 Smarca5 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5 gene MP:0012120 trophectoderm cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:14617767 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18094351 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:18094351 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:18094351 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18094351 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:18094351 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18094351 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18094351 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20180201 MGI PMID:18097012 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0001379 abnormal penile erection IAGP N RGD:5509061 20141003 MGI PMID:18094351 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:18094351 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18094351 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20180201 MGI PMID:18097012 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0002083 premature death IAGP N RGD:5509061 20180201 MGI PMID:18097012 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18094351 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0002750 exophthalmos IAGP N RGD:5509061 20180201 MGI PMID:18097012 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220811 MGI 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20180201 MGI PMID:8786307 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20180201 MGI PMID:8786307 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20180201 MGI PMID:8786307 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:18094351 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210826 MGI 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0010016 variable depigmentation IAGP N RGD:5509061 20180201 MGI PMID:18097012 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0010274 increased organ/body region tumor incidence IAGP N RGD:5509061 20180201 MGI PMID:18097012 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20180201 MGI PMID:18097012 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0010295 increased eye tumor incidence IAGP N RGD:5509061 20180201 MGI PMID:18097012 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:18094351 1623061 Immp2l IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:18094351 1623072 Ear6 eosinophil-associated, ribonuclease A family, member 6 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1623076 Pcdhga1 protocadherin gamma subfamily A, 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17572674 1623079 Pcdhgc3 protocadherin gamma subfamily C, 3 gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20211021 MGI 1623085 Pcdhgb2 protocadherin gamma subfamily B, 2 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20220811 MGI 1623086 Sec16b SEC16 homolog B, endoplasmic reticulum export factor gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20200310 MGI 1623086 Sec16b SEC16 homolog B, endoplasmic reticulum export factor gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20200310 MGI 1623086 Sec16b SEC16 homolog B, endoplasmic reticulum export factor gene MP:0001260 increased body weight IEA N RGD:5509061 20200310 MGI 1623086 Sec16b SEC16 homolog B, endoplasmic reticulum export factor gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200310 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0000613 abnormal salivary gland morphology IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0000618 small salivary gland IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180628 MGI PMID:26571211 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0002311 abnormal inspiratory capacity IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0003394 increased cardiac output IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0010895 increased lung compliance IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0011045 decreased lung elastance IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0011951 increased cardiac stroke volume IEA N RGD:5509061 20230601 MGI 1623087 Hycc1 hyccin PI4KA lipid kinase complex subunit 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 1623089 Selenok selenoprotein K gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21220695 1623089 Selenok selenoprotein K gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:21220695 1623089 Selenok selenoprotein K gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:21220695 1623089 Selenok selenoprotein K gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1623089 Selenok selenoprotein K gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20160421 MGI 1623089 Selenok selenoprotein K gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20201231 MGI 1623089 Selenok selenoprotein K gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 1623089 Selenok selenoprotein K gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21220695 1623089 Selenok selenoprotein K gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21220695 1623089 Selenok selenoprotein K gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21220695 1623089 Selenok selenoprotein K gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:21220695 1623089 Selenok selenoprotein K gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20211021 MGI 1623089 Selenok selenoprotein K gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1623089 Selenok selenoprotein K gene MP:0010093 decreased circulating magnesium level IEA N RGD:5509061 20181227 MGI 1623089 Selenok selenoprotein K gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:21220695 1623089 Selenok selenoprotein K gene MP:0020943 increased susceptibility to Flaviviridae infection IAGP N RGD:5509061 20200430 MGI PMID:21220695 1623089 Selenok selenoprotein K gene MP:0031044 increased susceptibility to Flaviviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:21220695 1623090 BC004004 cDNA sequence BC004004 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1623090 BC004004 cDNA sequence BC004004 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20220929 MGI PMID:35820707 1623090 BC004004 cDNA sequence BC004004 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20220929 MGI PMID:35820707 1623090 BC004004 cDNA sequence BC004004 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20220929 MGI PMID:35820707 1623090 BC004004 cDNA sequence BC004004 gene MP:0011807 decreased lung fibroblast proliferation IAGP N RGD:5509061 20220929 MGI PMID:35820707 1623090 BC004004 cDNA sequence BC004004 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20220929 MGI PMID:35820707 1623090 BC004004 cDNA sequence BC004004 gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20220929 MGI PMID:35820707 1623090 BC004004 cDNA sequence BC004004 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20220929 MGI PMID:35820707 1623090 BC004004 cDNA sequence BC004004 gene MP:0030679 decreased hydroxyproline level IAGP N RGD:5509061 20220929 MGI PMID:35820707 1623090 BC004004 cDNA sequence BC004004 gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20220929 MGI PMID:35820707 1623090 BC004004 cDNA sequence BC004004 gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20220929 MGI PMID:35820707 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20210520 MGI 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220519 MGI 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0011625 cystolithiasis IEA N RGD:5509061 20210520 MGI 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1623091 Cwc22 CWC22 spliceosome-associated protein gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0000277 abnormal heart shape IEA N RGD:5509061 20210520 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210826 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240627 MGI PMID:38835510 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20210520 MGI 1623096 Spz1 spermatogenic leucine zipper 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 1623099 Cox7b2 cytochrome c oxidase subunit 7B2 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20211021 MGI PMID:34326397 1623099 Cox7b2 cytochrome c oxidase subunit 7B2 gene MP:0001925 male infertility IAGP N RGD:5509061 20211021 MGI PMID:34326397 1623099 Cox7b2 cytochrome c oxidase subunit 7B2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20211021 MGI PMID:34326397 1623099 Cox7b2 cytochrome c oxidase subunit 7B2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20211021 MGI PMID:34326397 1623099 Cox7b2 cytochrome c oxidase subunit 7B2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20211021 MGI PMID:34326397 1623099 Cox7b2 cytochrome c oxidase subunit 7B2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20211021 MGI PMID:34326397 1623099 Cox7b2 cytochrome c oxidase subunit 7B2 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20211021 MGI PMID:34326397 1623102 Spata31 spermatogenesis associated 31 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20210325 MGI PMID:25930072 1623102 Spata31 spermatogenesis associated 31 gene MP:0001147 small testis IAGP N RGD:5509061 20210325 MGI PMID:25930072 1623102 Spata31 spermatogenesis associated 31 gene MP:0001925 male infertility IAGP N RGD:5509061 20210325 MGI PMID:25930072 1623102 Spata31 spermatogenesis associated 31 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210325 MGI PMID:25930072 1623102 Spata31 spermatogenesis associated 31 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20210325 MGI PMID:25930072 1623102 Spata31 spermatogenesis associated 31 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210325 MGI PMID:25930072 1623102 Spata31 spermatogenesis associated 31 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210325 MGI PMID:25930072 1623103 4930451I11Rik RIKEN cDNA 4930451I11 gene gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20201022 MGI PMID:32295885 1623103 4930451I11Rik RIKEN cDNA 4930451I11 gene gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20201022 MGI PMID:32295885 1623103 4930451I11Rik RIKEN cDNA 4930451I11 gene gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220811 MGI PMID:34982145 1623103 4930451I11Rik RIKEN cDNA 4930451I11 gene gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1623103 4930451I11Rik RIKEN cDNA 4930451I11 gene gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1623103 4930451I11Rik RIKEN cDNA 4930451I11 gene gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220811 MGI PMID:34982145 1623106 Golga1 golgin A1 gene MP:0000745 tremors IEA N RGD:5509061 20150730 MGI 1623106 Golga1 golgin A1 gene MP:0001304 cataract IEA N RGD:5509061 20150730 MGI 1623106 Golga1 golgin A1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20150730 MGI 1623106 Golga1 golgin A1 gene MP:0001513 limb grasping IEA N RGD:5509061 20150730 MGI 1623106 Golga1 golgin A1 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20150730 MGI 1623106 Golga1 golgin A1 gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20150730 MGI 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0000888 absent cerebellar granule layer IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0002958 cerebral aqueductal stenosis IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0009512 abnormal cerebellar Golgi cell morphology IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0009978 abnormal cerebellum white matter morphology IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0010540 long stride length IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0012004 abnormal septum pellucidum morphology IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0012508 forebrain atrophy IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0013258 abnormal extracellular matrix morphology IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0020141 decreased brain external capsule size IAGP N RGD:5509061 20161208 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0030003 hippocampus atrophy IAGP N RGD:5509061 20170706 MGI PMID:24614806 1623107 Bicd2 BICD cargo adaptor 2 gene MP:0030986 striatum atrophy IAGP N RGD:5509061 20191128 MGI PMID:24614806 1623108 Rab36 RAB36, member RAS oncogene family gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210826 MGI 1623108 Rab36 RAB36, member RAS oncogene family gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20240523 MGI 1623108 Rab36 RAB36, member RAS oncogene family gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1623108 Rab36 RAB36, member RAS oncogene family gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1623108 Rab36 RAB36, member RAS oncogene family gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20211021 MGI 1623108 Rab36 RAB36, member RAS oncogene family gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 1623108 Rab36 RAB36, member RAS oncogene family gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1623108 Rab36 RAB36, member RAS oncogene family gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1623109 Ccdc116 coiled-coil domain containing 116 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220811 MGI 1623111 Nlrp14 NLR family, pyrin domain containing 14 gene MP:0001926 female infertility IEA N RGD:5509061 20230601 MGI 1623111 Nlrp14 NLR family, pyrin domain containing 14 gene MP:0003718 maternal effect IAGP N RGD:5509061 20230323 MGI PMID:36539615 1623112 Hyls1 HYLS1, centriolar and ciliogenesis associated gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20190502 MGI 1623112 Hyls1 HYLS1, centriolar and ciliogenesis associated gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 1623112 Hyls1 HYLS1, centriolar and ciliogenesis associated gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20181227 MGI 1623112 Hyls1 HYLS1, centriolar and ciliogenesis associated gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1623112 Hyls1 HYLS1, centriolar and ciliogenesis associated gene MP:0004357 long tibia IEA N RGD:5509061 20190502 MGI 1623112 Hyls1 HYLS1, centriolar and ciliogenesis associated gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1623112 Hyls1 HYLS1, centriolar and ciliogenesis associated gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200402 MGI 1623112 Hyls1 HYLS1, centriolar and ciliogenesis associated gene MP:0011953 prolonged PQ interval IEA N RGD:5509061 20210826 MGI 1623112 Hyls1 HYLS1, centriolar and ciliogenesis associated gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1623114 Cyria CYFIP related Rac1 interactor A gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230119 MGI 1623114 Cyria CYFIP related Rac1 interactor A gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230119 MGI 1623114 Cyria CYFIP related Rac1 interactor A gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20230119 MGI 1623114 Cyria CYFIP related Rac1 interactor A gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230119 MGI 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141225 MGI PMID:25088364 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141225 MGI PMID:25088364 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141225 MGI PMID:25088364 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0001925 male infertility IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0002001 blindness IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141225 MGI PMID:25088364 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141225 MGI PMID:25088364 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0011065 abnormal kidney epithelial cell primary cilium morphology IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141225 MGI PMID:25088364 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0011308 kidney corticomedullary cyst IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0011308 kidney corticomedullary cyst IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0011376 abnormal kidney corticomedullary boundary morphology IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20160211 MGI PMID:24722439 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0013205 abnormal nonmotile primary cilium morphology IAGP N RGD:5509061 20141225 MGI PMID:25088364 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0020383 decreased kidney epithelial cell primary cilium length IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0020384 absent kidney epithelial cell primary cilium IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623115 Sdccag8 serologically defined colon cancer antigen 8 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20220929 MGI PMID:35503560 1623116 Calcoco2 calcium binding and coiled-coil domain 2 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20201231 MGI 1623118 Zfp998 zinc finger protein 998 gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20210415 MGI PMID:30709743 1623118 Zfp998 zinc finger protein 998 gene MP:0020845 abnormal DNA-templated transcription IAGP N RGD:5509061 20210415 MGI PMID:30709743 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0001258 decreased body length IEA N RGD:5509061 20160804 MGI 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0001304 cataract IAGP N RGD:5509061 20160922 MGI PMID:24652767 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160922 MGI PMID:24652767 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20160922 MGI PMID:24652767 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20160922 MGI PMID:24652767 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20160804 MGI 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20160804 MGI 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20160922 MGI PMID:24652767 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20160804 MGI 1623119 Usp42 ubiquitin specific peptidase 42 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20160922 MGI PMID:24652767 1623120 Pcdh1 protocadherin 1 gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20201022 MGI 1623121 Krtap9-3 keratin associated protein 9-3 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20231207 MGI 1623121 Krtap9-3 keratin associated protein 9-3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1623121 Krtap9-3 keratin associated protein 9-3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 1623121 Krtap9-3 keratin associated protein 9-3 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20231207 MGI 1623121 Krtap9-3 keratin associated protein 9-3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 1623121 Krtap9-3 keratin associated protein 9-3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1623124 Spata9 spermatogenesis associated 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18775323 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0000705 athymia IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23207905 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0000726 absent lymphocyte IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18775323 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:17360556 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:18775323 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18775323 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18775323 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:18775323 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200402 MGI PMID:30017584 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:17360556 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:18775323 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200402 MGI PMID:30017584 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:18775323 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23207905 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18775323 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:23207905 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:17360556 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18775323 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:18775323 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:23207905 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20211118 MGI PMID:32355287 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:23207905 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23207905 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23207905 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20200402 MGI PMID:30017584 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623125 Nhej1 non-homologous end joining factor 1 gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20170413 MGI PMID:27798842 1623127 Spata45 spermatogenesis associated 45 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38697008 1623129 Akap13 A kinase anchor protein 13 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:20139090 1623129 Akap13 A kinase anchor protein 13 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:20139090 1623129 Akap13 A kinase anchor protein 13 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1623129 Akap13 A kinase anchor protein 13 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1623129 Akap13 A kinase anchor protein 13 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 1623129 Akap13 A kinase anchor protein 13 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 1623129 Akap13 A kinase anchor protein 13 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:19211510 1623129 Akap13 A kinase anchor protein 13 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19211510 1623129 Akap13 A kinase anchor protein 13 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1623129 Akap13 A kinase anchor protein 13 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 1623129 Akap13 A kinase anchor protein 13 gene MP:0001304 cataract IEA N RGD:5509061 20210826 MGI 1623129 Akap13 A kinase anchor protein 13 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1623129 Akap13 A kinase anchor protein 13 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:20139090 1623129 Akap13 A kinase anchor protein 13 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 1623129 Akap13 A kinase anchor protein 13 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1623129 Akap13 A kinase anchor protein 13 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:23658642 1623129 Akap13 A kinase anchor protein 13 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1623129 Akap13 A kinase anchor protein 13 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:20139090 1623129 Akap13 A kinase anchor protein 13 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1623129 Akap13 A kinase anchor protein 13 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16469733 1623129 Akap13 A kinase anchor protein 13 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20139090 1623129 Akap13 A kinase anchor protein 13 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:20139090 1623129 Akap13 A kinase anchor protein 13 gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20170309 MGI PMID:23658642 1623129 Akap13 A kinase anchor protein 13 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19211510 1623129 Akap13 A kinase anchor protein 13 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19211510 1623129 Akap13 A kinase anchor protein 13 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20210520 MGI 1623129 Akap13 A kinase anchor protein 13 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20231207 MGI 1623129 Akap13 A kinase anchor protein 13 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:20139090 1623129 Akap13 A kinase anchor protein 13 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20170309 MGI PMID:23658642 1623129 Akap13 A kinase anchor protein 13 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:20139090 1623129 Akap13 A kinase anchor protein 13 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19211510 1623129 Akap13 A kinase anchor protein 13 gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19211510 1623129 Akap13 A kinase anchor protein 13 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:19211510 1623129 Akap13 A kinase anchor protein 13 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20210520 MGI 1623129 Akap13 A kinase anchor protein 13 gene MP:0009922 increased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:19211510 1623129 Akap13 A kinase anchor protein 13 gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:19211510 1623129 Akap13 A kinase anchor protein 13 gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20139090 1623129 Akap13 A kinase anchor protein 13 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16469733 1623129 Akap13 A kinase anchor protein 13 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20139090 1623129 Akap13 A kinase anchor protein 13 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:20139090 1623129 Akap13 A kinase anchor protein 13 gene MP:0012723 abnormal nuchal region morphology IAGP N RGD:5509061 20141003 MGI PMID:20139090 1623129 Akap13 A kinase anchor protein 13 gene MP:0014348 decreased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:19211510 1623129 Akap13 A kinase anchor protein 13 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:23658642 1623130 Tslrn1 testis specific long noncoding RNA 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210603 MGI PMID:29044429 1623132 Nme5 NME/NM23 family member 5 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:21746835 1623132 Nme5 NME/NM23 family member 5 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21746835 1623132 Nme5 NME/NM23 family member 5 gene MP:0001866 nasal inflammation IAGP N RGD:5509061 20171005 MGI PMID:21746835 1623132 Nme5 NME/NM23 family member 5 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21746835 1623132 Nme5 NME/NM23 family member 5 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21746835 1623132 Nme5 NME/NM23 family member 5 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:21746835 1623132 Nme5 NME/NM23 family member 5 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:21746835 1623132 Nme5 NME/NM23 family member 5 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:21746835 1623132 Nme5 NME/NM23 family member 5 gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:21746835 1623132 Nme5 NME/NM23 family member 5 gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20141003 MGI PMID:21746835 1623132 Nme5 NME/NM23 family member 5 gene MP:0030113 maxillary sinus inflammation IAGP N RGD:5509061 20171005 MGI PMID:21746835 1623135 Tex29 testis expressed 29 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 1623135 Tex29 testis expressed 29 gene MP:0001513 limb grasping IEA N RGD:5509061 20181227 MGI 1623135 Tex29 testis expressed 29 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1623138 Ttc32 tetratricopeptide repeat domain 32 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 1623140 Izumo2 IZUMO family member 2 gene MP:0002626 increased heart rate IEA N RGD:5509061 20220519 MGI 1623140 Izumo2 IZUMO family member 2 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20220519 MGI 1623142 Cmtm2b CKLF-like MARVEL transmembrane domain containing 2B gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20190926 MGI PMID:30209135 1623142 Cmtm2b CKLF-like MARVEL transmembrane domain containing 2B gene MP:0001925 male infertility IAGP N RGD:5509061 20190926 MGI PMID:30209135 1623142 Cmtm2b CKLF-like MARVEL transmembrane domain containing 2B gene MP:0020869 immotile sperm IAGP N RGD:5509061 20190926 MGI PMID:30209135 1623142 Cmtm2b CKLF-like MARVEL transmembrane domain containing 2B gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20200102 MGI PMID:30209135 1623145 Spem1 spermatid maturation 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:17426145 1623145 Spem1 spermatid maturation 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17426145 1623145 Spem1 spermatid maturation 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17426145 1623145 Spem1 spermatid maturation 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17426145 1623145 Spem1 spermatid maturation 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17426145 1623145 Spem1 spermatid maturation 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17426145 1623145 Spem1 spermatid maturation 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:17426145 1623148 Spatc1 spermatogenesis and centriole associated 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20240523 MGI 1623148 Spatc1 spermatogenesis and centriole associated 1 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20240523 MGI 1623149 Chic2 cysteine-rich hydrophobic domain 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200402 MGI 1623149 Chic2 cysteine-rich hydrophobic domain 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200402 MGI 1623149 Chic2 cysteine-rich hydrophobic domain 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160421 MGI 1623149 Chic2 cysteine-rich hydrophobic domain 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1623149 Chic2 cysteine-rich hydrophobic domain 2 gene MP:0004222 iris synechia IEA N RGD:5509061 20160421 MGI 1623149 Chic2 cysteine-rich hydrophobic domain 2 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20200402 MGI 1623149 Chic2 cysteine-rich hydrophobic domain 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 1623149 Chic2 cysteine-rich hydrophobic domain 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1623150 Aven apoptosis, caspase activation inhibitor gene MP:0001648 abnormal apoptosis IEA N RGD:5509061 20141003 MGI 1623150 Aven apoptosis, caspase activation inhibitor gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230119 MGI 1623151 Klrg2 killer cell lectin-like receptor subfamily G, member 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 1623154 Chpf chondroitin polymerizing factor gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20201231 MGI 1623154 Chpf chondroitin polymerizing factor gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 1623154 Chpf chondroitin polymerizing factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22952769 1623154 Chpf chondroitin polymerizing factor gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:22952769 1623154 Chpf chondroitin polymerizing factor gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:22952769 1623154 Chpf chondroitin polymerizing factor gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 1623155 Tubgcp2 tubulin, gamma complex component 2 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1623155 Tubgcp2 tubulin, gamma complex component 2 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241017 MGI 1623155 Tubgcp2 tubulin, gamma complex component 2 gene MP:0004964 absent inner cell mass IEA N RGD:5509061 20241017 MGI 1623155 Tubgcp2 tubulin, gamma complex component 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 1623155 Tubgcp2 tubulin, gamma complex component 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1623155 Tubgcp2 tubulin, gamma complex component 2 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241017 MGI 1623156 Liat1 ligand of ATE1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 1623156 Liat1 ligand of ATE1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 1623156 Liat1 ligand of ATE1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 1623156 Liat1 ligand of ATE1 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20230601 MGI 1623158 Septin14 septin 14 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230119 MGI 1623158 Septin14 septin 14 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 1623158 Septin14 septin 14 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1623158 Septin14 septin 14 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 1623158 Septin14 septin 14 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20230824 MGI PMID:35571367 1623158 Septin14 septin 14 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230119 MGI 1623158 Septin14 septin 14 gene MP:0003999 enhanced passive avoidance behavior IAGP N RGD:5509061 20230824 MGI PMID:35571367 1623158 Septin14 septin 14 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230119 MGI 1623158 Septin14 septin 14 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 1623158 Septin14 septin 14 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20230824 MGI PMID:35571367 1623158 Septin14 septin 14 gene MP:0012206 increased neuronal stem cell self-renewal IAGP N RGD:5509061 20230824 MGI PMID:35571367 1623159 Spmip9 sperm microtubule inner protein 9 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1623161 1700016H13Rik RIKEN cDNA 1700016H13 gene gene MP:0005534 decreased body temperature IEA N RGD:5509061 20210128 MGI 1623164 Kantr Kdm5c adjacent non-coding transcript gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:24381249 1623166 Fbxo47 F-box protein 47 gene MP:0001147 small testis IAGP N RGD:5509061 20220428 MGI PMID:35310947 1623166 Fbxo47 F-box protein 47 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220428 MGI PMID:35310947 1623166 Fbxo47 F-box protein 47 gene MP:0001925 male infertility IAGP N RGD:5509061 20220428 MGI PMID:35310947 1623166 Fbxo47 F-box protein 47 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220428 MGI PMID:35310947 1623166 Fbxo47 F-box protein 47 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20220428 MGI PMID:35310947 1623166 Fbxo47 F-box protein 47 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 1623166 Fbxo47 F-box protein 47 gene MP:0011752 abnormal X-Y chromosome synaptonemal complex assembly during male meiosis IAGP N RGD:5509061 20220428 MGI PMID:35310947 1623166 Fbxo47 F-box protein 47 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220428 MGI PMID:35310947 1623169 Ift25 intraflagellar transport 25 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20160804 MGI 1623169 Ift25 intraflagellar transport 25 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0003443 increased circulating glycerol level IEA N RGD:5509061 20160804 MGI 1623169 Ift25 intraflagellar transport 25 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1623169 Ift25 intraflagellar transport 25 gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623169 Ift25 intraflagellar transport 25 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1623169 Ift25 intraflagellar transport 25 gene MP:0011673 unbalanced complete common atrioventricular canal IAGP N RGD:5509061 20141003 MGI PMID:22595669 1623170 Slc41a3 solute carrier family 41, member 3 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20161117 MGI PMID:27349617 1623170 Slc41a3 solute carrier family 41, member 3 gene MP:0001513 limb grasping IEA N RGD:5509061 20160804 MGI 1623170 Slc41a3 solute carrier family 41, member 3 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20161117 MGI PMID:27349617 1623170 Slc41a3 solute carrier family 41, member 3 gene MP:0003588 ureter stenosis IAGP N RGD:5509061 20161117 MGI PMID:27349617 1623170 Slc41a3 solute carrier family 41, member 3 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20161117 MGI PMID:27349617 1623170 Slc41a3 solute carrier family 41, member 3 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20240404 MGI PMID:36049064 1623170 Slc41a3 solute carrier family 41, member 3 gene MP:0011979 abnormal magnesium ion homeostasis IAGP N RGD:5509061 20161117 MGI PMID:27349617 1623172 Gypc glycophorin C gene MP:0006352 decreased glycosylated hemoglobin level IEA N RGD:5509061 20210128 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20231207 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20231207 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20181227 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0000495 abnormal colon morphology IEA N RGD:5509061 20181227 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0000642 enlarged adrenal glands IEA N RGD:5509061 20170105 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0000692 small spleen IEA N RGD:5509061 20170105 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0000706 small thymus IEA N RGD:5509061 20170105 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20170105 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0001258 decreased body length IEA N RGD:5509061 20181227 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20181227 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0002175 decreased brain weight IEA N RGD:5509061 20220519 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0002731 megacolon IEA N RGD:5509061 20170105 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20201022 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20231207 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20181227 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0003402 decreased liver weight IEA N RGD:5509061 20211021 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0003655 absent pancreas IEA N RGD:5509061 20170105 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0004002 abnormal jejunum morphology IEA N RGD:5509061 20181227 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20220811 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0004956 decreased thymus weight IEA N RGD:5509061 20220519 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20170105 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0009483 enlarged ileum IEA N RGD:5509061 20170105 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20181227 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0011503 distended jejunum IEA N RGD:5509061 20170105 MGI 1623173 Tmem248 transmembrane protein 248 gene MP:0011882 enlarged duodenum IEA N RGD:5509061 20170105 MGI 1623175 Zfp949 zinc finger protein 949 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20180503 MGI PMID:27196371 1623175 Zfp949 zinc finger protein 949 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20180503 MGI PMID:27196371 1623175 Zfp949 zinc finger protein 949 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180503 MGI PMID:27196371 1623175 Zfp949 zinc finger protein 949 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20180503 MGI PMID:27196371 1623175 Zfp949 zinc finger protein 949 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180503 MGI PMID:27196371 1623175 Zfp949 zinc finger protein 949 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20180503 MGI PMID:27196371 1623175 Zfp949 zinc finger protein 949 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20180503 MGI PMID:27196371 1623175 Zfp949 zinc finger protein 949 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180503 MGI PMID:27196371 1623175 Zfp949 zinc finger protein 949 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20180503 MGI PMID:27196371 1623175 Zfp949 zinc finger protein 949 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20180503 MGI PMID:27196371 1623175 Zfp949 zinc finger protein 949 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20180503 MGI PMID:27196371 1623177 Arl14 ADP-ribosylation factor-like 14 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 1623178 Tradd TNFRSF1A-associated via death domain gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:18641654 1623178 Tradd TNFRSF1A-associated via death domain gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18719121 1623178 Tradd TNFRSF1A-associated via death domain gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:18641654 1623178 Tradd TNFRSF1A-associated via death domain gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18641654 1623178 Tradd TNFRSF1A-associated via death domain gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:18719121 1623178 Tradd TNFRSF1A-associated via death domain gene MP:0008473 abnormal spleen follicular dendritic cell network IAGP N RGD:5509061 20141003 MGI PMID:18719121 1623178 Tradd TNFRSF1A-associated via death domain gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:18719121 1623178 Tradd TNFRSF1A-associated via death domain gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:18641654 1623178 Tradd TNFRSF1A-associated via death domain gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:18439848 1623178 Tradd TNFRSF1A-associated via death domain gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18719121 1623178 Tradd TNFRSF1A-associated via death domain gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:18719121 1623178 Tradd TNFRSF1A-associated via death domain gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:18641654 1623178 Tradd TNFRSF1A-associated via death domain gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18641653 1623178 Tradd TNFRSF1A-associated via death domain gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18641654 1623178 Tradd TNFRSF1A-associated via death domain gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:18719121 1623180 Kptn kaptin gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20160804 MGI 1623180 Kptn kaptin gene MP:0000434 megacephaly IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0000441 increased cranium width IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23870131 1623180 Kptn kaptin gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23870131 1623180 Kptn kaptin gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20141003 MGI 1623180 Kptn kaptin gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 1623180 Kptn kaptin gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 1623180 Kptn kaptin gene MP:0005238 increased brain size IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20141003 MGI 1623180 Kptn kaptin gene MP:0008283 small hippocampus IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20141003 MGI 1623180 Kptn kaptin gene MP:0011812 increased cranium length IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0011861 increased cranium height IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0012443 increased corpus callosum size IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0012449 increased primary motor cortex size IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0012461 increased brain internal capsule size IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0013908 small lateral ventricles IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0020593 increased cerebral cortex cell number IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0020597 increased cerebral cortex total cell area IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0030262 frontal bossing IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623180 Kptn kaptin gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20240314 MGI PMID:37437211 1623182 Kctd2 potassium channel tetramerisation domain containing 2 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20230119 MGI 1623185 Actl10 actin-like 10 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 1623186 Polr1g RNA polymerase I subunit G gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230720 MGI 1623186 Polr1g RNA polymerase I subunit G gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230720 MGI 1623187 Arl16 ADP-ribosylation factor-like 16 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1623187 Arl16 ADP-ribosylation factor-like 16 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1623187 Arl16 ADP-ribosylation factor-like 16 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 1623187 Arl16 ADP-ribosylation factor-like 16 gene MP:0000692 small spleen IEA N RGD:5509061 20230601 MGI 1623187 Arl16 ADP-ribosylation factor-like 16 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1623187 Arl16 ADP-ribosylation factor-like 16 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1623187 Arl16 ADP-ribosylation factor-like 16 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230601 MGI 1623187 Arl16 ADP-ribosylation factor-like 16 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1623187 Arl16 ADP-ribosylation factor-like 16 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1623187 Arl16 ADP-ribosylation factor-like 16 gene MP:0001262 decreased body weight IEA N RGD:5509061 20230601 MGI 1623187 Arl16 ADP-ribosylation factor-like 16 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 1623187 Arl16 ADP-ribosylation factor-like 16 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1623187 Arl16 ADP-ribosylation factor-like 16 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20240523 MGI 1623187 Arl16 ADP-ribosylation factor-like 16 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20240523 MGI 1623187 Arl16 ADP-ribosylation factor-like 16 gene MP:0004083 polysyndactyly IEA N RGD:5509061 20230601 MGI 1623188 Tmem160 transmembrane protein 160 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1623188 Tmem160 transmembrane protein 160 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1623188 Tmem160 transmembrane protein 160 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 1623188 Tmem160 transmembrane protein 160 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20230817 MGI PMID:34936870 1623188 Tmem160 transmembrane protein 160 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20220519 MGI 1623188 Tmem160 transmembrane protein 160 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1623188 Tmem160 transmembrane protein 160 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20230817 MGI PMID:34936870 1623188 Tmem160 transmembrane protein 160 gene MP:0005316 abnormal response to tactile stimuli IAGP N RGD:5509061 20230817 MGI PMID:34936870 1623188 Tmem160 transmembrane protein 160 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20230817 MGI PMID:34936870 1623188 Tmem160 transmembrane protein 160 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0001241 absent epidermis stratum corneum IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0009576 oral atresia IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0009884 palatal shelf fusion with tongue or mandible IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24075906 1623191 Kdf1 keratinocyte differentiation factor 1 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:24075906 1623192 Tmem273 transmembrane protein 273 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20210520 MGI 1623192 Tmem273 transmembrane protein 273 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20200514 MGI 1623192 Tmem273 transmembrane protein 273 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 1623192 Tmem273 transmembrane protein 273 gene MP:0003036 vertebral transformation IEA N RGD:5509061 20200514 MGI 1623192 Tmem273 transmembrane protein 273 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20200514 MGI 1623193 Tcim transcriptional and immune response regulator gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0008247 abnormal mononuclear cell morphology IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0013693 abnormal hemopoiesis IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0013696 increased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623193 Tcim transcriptional and immune response regulator gene MP:0013891 increased common myeloid progenitor cell number IAGP N RGD:5509061 20160804 MGI PMID:24937306 1623195 Atp2c2 ATPase, Ca++ transporting, type 2C, member 2 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20181227 MGI 1623195 Atp2c2 ATPase, Ca++ transporting, type 2C, member 2 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1623195 Atp2c2 ATPase, Ca++ transporting, type 2C, member 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1623195 Atp2c2 ATPase, Ca++ transporting, type 2C, member 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 1623196 Tmem258 transmembrane protein 258 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20170608 MGI PMID:27974209 1623196 Tmem258 transmembrane protein 258 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20170608 MGI PMID:27974209 1623196 Tmem258 transmembrane protein 258 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20170608 MGI PMID:27974209 1623196 Tmem258 transmembrane protein 258 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20170608 MGI PMID:27974209 1623196 Tmem258 transmembrane protein 258 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20170608 MGI PMID:27974209 1623196 Tmem258 transmembrane protein 258 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20170608 MGI PMID:27974209 1623196 Tmem258 transmembrane protein 258 gene MP:0012556 increased cell death IAGP N RGD:5509061 20170608 MGI PMID:27974209 1623196 Tmem258 transmembrane protein 258 gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20170608 MGI PMID:27974209 1623196 Tmem258 transmembrane protein 258 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20170608 MGI PMID:27974209 1623196 Tmem258 transmembrane protein 258 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20170608 MGI PMID:27974209 1623197 Anapc13 anaphase promoting complex subunit 13 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20190502 MGI 1623197 Anapc13 anaphase promoting complex subunit 13 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1623197 Anapc13 anaphase promoting complex subunit 13 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20190502 MGI 1623197 Anapc13 anaphase promoting complex subunit 13 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623197 Anapc13 anaphase promoting complex subunit 13 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20191128 MGI 1623197 Anapc13 anaphase promoting complex subunit 13 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20220519 MGI 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0000745 tremors IEA N RGD:5509061 20220811 MGI 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20210513 MGI PMID:32115408 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0001127 small ovary IEA N RGD:5509061 20220519 MGI 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210513 MGI PMID:32115408 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0002176 increased brain weight IAGP N RGD:5509061 20210513 MGI PMID:32115408 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20210513 MGI PMID:32115408 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0002834 decreased heart weight IEA N RGD:5509061 20230601 MGI 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20210826 MGI 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0005238 increased brain size IAGP N RGD:5509061 20210513 MGI PMID:32115408 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20231123 MGI PMID:34761259 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20231123 MGI PMID:34761259 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0009709 hydrometra IEA N RGD:5509061 20220519 MGI 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20231123 MGI PMID:34761259 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20210513 MGI PMID:32115408 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20220519 MGI 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0020507 increased dendritic spine density IAGP N RGD:5509061 20231123 MGI PMID:34761259 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0020593 increased cerebral cortex cell number IAGP N RGD:5509061 20210513 MGI PMID:32115408 1623199 Rab39b RAB39B, member RAS oncogene family gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20231123 MGI PMID:34761259 1623200 Dalrd3 DALR anticodon binding domain containing 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1623201 Zfp639 zinc finger protein 639 gene MP:0013891 increased common myeloid progenitor cell number IAGP N RGD:5509061 20210617 MGI PMID:23617998 1623201 Zfp639 zinc finger protein 639 gene MP:0020935 decreased susceptibility to Retroviridae infection IAGP N RGD:5509061 20210617 MGI PMID:23617998 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0000434 megacephaly IAGP N RGD:5509061 20180802 MGI PMID:27602517 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20180802 MGI PMID:27602517 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20180802 MGI PMID:27602517 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:30104731 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20200310 MGI PMID:30104731 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20180802 MGI PMID:27602517 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:15367660 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:15367660 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15367660 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200310 MGI PMID:30104731 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20180802 MGI PMID:27602517 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20200310 MGI PMID:30104731 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20200310 MGI PMID:30104731 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:15367660 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20200310 MGI PMID:30104731 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20180802 MGI PMID:27602517 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0003895 increased ectoderm apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15367660 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20200310 MGI PMID:30104731 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:15367660 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20240523 MGI 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20240523 MGI 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20180802 MGI PMID:27602517 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20180802 MGI PMID:27602517 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20200310 MGI PMID:30104731 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15367660 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180802 MGI PMID:27602517 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0012315 impaired learning IAGP N RGD:5509061 20180802 MGI PMID:27602517 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0013140 excessive vocalization IAGP N RGD:5509061 20200310 MGI PMID:30104731 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0013916 decreased intestine length IAGP N RGD:5509061 20180802 MGI PMID:27602517 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:30104731 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:30104731 1623202 Chd8 chromodomain helicase DNA binding protein 8 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:30104731 1623203 Caap1 caspase activity and apoptosis inhibitor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210128 MGI PMID:30629682 1623204 Jagn1 jagunal homolog 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141204 MGI PMID:25129145 1623204 Jagn1 jagunal homolog 1 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141204 MGI PMID:25129145 1623204 Jagn1 jagunal homolog 1 gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141204 MGI PMID:25129145 1623204 Jagn1 jagunal homolog 1 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141204 MGI PMID:25129145 1623204 Jagn1 jagunal homolog 1 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141204 MGI PMID:25129145 1623205 Eqtn equatorin, sperm acrosome associated gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20190131 MGI PMID:24480441 1623205 Eqtn equatorin, sperm acrosome associated gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20190131 MGI PMID:24480441 1623205 Eqtn equatorin, sperm acrosome associated gene MP:0001935 decreased litter size IAGP N RGD:5509061 20190131 MGI PMID:24480441 1623205 Eqtn equatorin, sperm acrosome associated gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20190131 MGI PMID:24480441 1623205 Eqtn equatorin, sperm acrosome associated gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20190131 MGI PMID:24480441 1623205 Eqtn equatorin, sperm acrosome associated gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20190131 MGI PMID:24480441 1623207 Mgarp mitochondria localized glutamic acid rich protein gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20240502 MGI PMID:24323429 1623207 Mgarp mitochondria localized glutamic acid rich protein gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20240502 MGI PMID:24323429 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20230601 MGI 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0001577 anemia IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12904583 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0003952 abnormal copper level IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0020148 abnormal susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0020879 abnormal calcium level IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0020891 abnormal sulfate level IAGP N RGD:5509061 20210610 MGI PMID:31571584 1623208 Slc48a1 solute carrier family 48 (heme transporter), member 1 gene MP:0031276 abnormal stress erythropoiesis IAGP N RGD:5509061 20210805 MGI PMID:31571584 1623210 Dph2 DPH2 homolog gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623211 Nudt13 nudix hydrolase 13 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1623211 Nudt13 nudix hydrolase 13 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 1623211 Nudt13 nudix hydrolase 13 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 1623214 Dnajc19 DnaJ heat shock protein family (Hsp40) member C19 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 1623214 Dnajc19 DnaJ heat shock protein family (Hsp40) member C19 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 1623214 Dnajc19 DnaJ heat shock protein family (Hsp40) member C19 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20141003 MGI 1623217 Polr2l polymerase (RNA) II (DNA directed) polypeptide L gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 1623217 Polr2l polymerase (RNA) II (DNA directed) polypeptide L gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1623217 Polr2l polymerase (RNA) II (DNA directed) polypeptide L gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1623219 Taf12 TATA-box binding protein associated factor 12 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20240919 MGI 1623219 Taf12 TATA-box binding protein associated factor 12 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20240606 MGI PMID:38593904 1623219 Taf12 TATA-box binding protein associated factor 12 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20240606 MGI PMID:38593904 1623219 Taf12 TATA-box binding protein associated factor 12 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20201022 MGI 1623219 Taf12 TATA-box binding protein associated factor 12 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20201022 MGI 1623219 Taf12 TATA-box binding protein associated factor 12 gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20240801 MGI PMID:38593904 1623219 Taf12 TATA-box binding protein associated factor 12 gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20201022 MGI 1623219 Taf12 TATA-box binding protein associated factor 12 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20240606 MGI PMID:38593904 1623219 Taf12 TATA-box binding protein associated factor 12 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20240606 MGI PMID:38593904 1623219 Taf12 TATA-box binding protein associated factor 12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623219 Taf12 TATA-box binding protein associated factor 12 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1623219 Taf12 TATA-box binding protein associated factor 12 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240919 MGI 1623220 Rex1bd required for excision 1-B domain containing gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 1623220 Rex1bd required for excision 1-B domain containing gene MP:0011953 prolonged PQ interval IEA N RGD:5509061 20231207 MGI 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20170706 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20170706 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20170706 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20170713 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160804 MGI 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20170706 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20170706 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20170706 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20170713 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20170706 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20170713 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20170713 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20170713 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20170713 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20170713 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20170713 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21615689 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20170706 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20170706 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20170706 MGI PMID:27207593 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20190124 MGI PMID:29674119 1623222 Nmnat1 nicotinamide nucleotide adenylyltransferase 1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:27207593 1623224 Spc25 SPC25, NDC80 kinetochore complex component, homolog (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623224 Spc25 SPC25, NDC80 kinetochore complex component, homolog (S. cerevisiae) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1623226 Borcs7 BLOC-1 related complex subunit 7 gene MP:0001393 ataxia IAGP N RGD:5509061 20190523 MGI PMID:30067980 1623226 Borcs7 BLOC-1 related complex subunit 7 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20190523 MGI PMID:30067980 1623226 Borcs7 BLOC-1 related complex subunit 7 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190523 MGI PMID:30067980 1623226 Borcs7 BLOC-1 related complex subunit 7 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20190523 MGI PMID:30067980 1623226 Borcs7 BLOC-1 related complex subunit 7 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20190523 MGI PMID:30067980 1623226 Borcs7 BLOC-1 related complex subunit 7 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20190523 MGI PMID:30067980 1623226 Borcs7 BLOC-1 related complex subunit 7 gene MP:0001513 limb grasping IAGP N RGD:5509061 20190523 MGI PMID:30067980 1623226 Borcs7 BLOC-1 related complex subunit 7 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20190523 MGI PMID:30067980 1623226 Borcs7 BLOC-1 related complex subunit 7 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20190523 MGI PMID:30067980 1623226 Borcs7 BLOC-1 related complex subunit 7 gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20190523 MGI PMID:30067980 1623226 Borcs7 BLOC-1 related complex subunit 7 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20190523 MGI PMID:30067980 1623226 Borcs7 BLOC-1 related complex subunit 7 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20190523 MGI PMID:30067980 1623226 Borcs7 BLOC-1 related complex subunit 7 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20190523 MGI PMID:30067980 1623226 Borcs7 BLOC-1 related complex subunit 7 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20190523 MGI PMID:30067980 1623227 Hamp2 hepcidin antimicrobial peptide 2 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:20053755 1623228 Uggt2 UDP-glucose glycoprotein glucosyltransferase 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20240523 MGI 1623228 Uggt2 UDP-glucose glycoprotein glucosyltransferase 2 gene MP:0002581 abnormal ileum morphology IEA N RGD:5509061 20240523 MGI 1623228 Uggt2 UDP-glucose glycoprotein glucosyltransferase 2 gene MP:0003959 abnormal lean body mass IEA N RGD:5509061 20240523 MGI 1623229 Chchd7 coiled-coil-helix-coiled-coil-helix domain containing 7 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1623229 Chchd7 coiled-coil-helix-coiled-coil-helix domain containing 7 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20181227 MGI 1623229 Chchd7 coiled-coil-helix-coiled-coil-helix domain containing 7 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1623230 Slc7a6os solute carrier family 7, member 6 opposite strand gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1623232 Pcp4l1 Purkinje cell protein 4-like 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230119 MGI 1623232 Pcp4l1 Purkinje cell protein 4-like 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230119 MGI 1623233 Coprs coordinator of PRMT5, differentiation stimulator gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25681392 1623233 Coprs coordinator of PRMT5, differentiation stimulator gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20160929 MGI PMID:25681392 1623233 Coprs coordinator of PRMT5, differentiation stimulator gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20160929 MGI PMID:25681392 1623233 Coprs coordinator of PRMT5, differentiation stimulator gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20160929 MGI PMID:25681392 1623233 Coprs coordinator of PRMT5, differentiation stimulator gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20160929 MGI PMID:25681392 1623233 Coprs coordinator of PRMT5, differentiation stimulator gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20160929 MGI PMID:25681392 1623236 Alkbh7 alkB homolog 7 gene MP:0001261 obese IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20210204 MGI PMID:32795389 1623236 Alkbh7 alkB homolog 7 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20210204 MGI PMID:32795389 1623236 Alkbh7 alkB homolog 7 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20210204 MGI PMID:32795389 1623236 Alkbh7 alkB homolog 7 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20210204 MGI PMID:32795389 1623236 Alkbh7 alkB homolog 7 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0008403 decreased cellular sensitivity to alkylating agents IAGP N RGD:5509061 20210204 MGI PMID:28726787 1623236 Alkbh7 alkB homolog 7 gene MP:0008405 decreased cellular sensitivity to methylmethanesulfonate IAGP N RGD:5509061 20210204 MGI PMID:28726787 1623236 Alkbh7 alkB homolog 7 gene MP:0008407 decreased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20210204 MGI PMID:28726787 1623236 Alkbh7 alkB homolog 7 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20210204 MGI PMID:28726787 1623236 Alkbh7 alkB homolog 7 gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210204 MGI PMID:28726787 1623236 Alkbh7 alkB homolog 7 gene MP:0010953 abnormal fatty acid oxidation IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0020102 increased hepatic glucose production IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623236 Alkbh7 alkB homolog 7 gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20210204 MGI PMID:23572141 1623237 Bean1 brain expressed, associated with Nedd4, 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20200514 MGI 1623237 Bean1 brain expressed, associated with Nedd4, 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141211 MGI 1623237 Bean1 brain expressed, associated with Nedd4, 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1623237 Bean1 brain expressed, associated with Nedd4, 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1623238 Arl6ip6 ADP-ribosylation factor-like 6 interacting protein 6 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20230601 MGI 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12410230 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22721776 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16702402 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18079696 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12410230 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18079696 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22721776 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20573698 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0003121 genetic imprinting IAGP N RGD:5509061 20141003 MGI PMID:18079696 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:12410230 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:12410230 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:16702402 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:18039841 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:18079696 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:20573698 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:22721776 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:12410230 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:18079696 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:12410230 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:20573698 1623239 Kcnq1ot1 KCNQ1 overlapping transcript 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:22721776 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:19246514 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0001433 polyphagia IAGP N RGD:5509061 20200310 MGI PMID:16985211 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0001762 polyuria IAGP N RGD:5509061 20200310 MGI PMID:16985211 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0001762 polyuria IAGP N RGD:5509061 20200310 MGI PMID:17167413 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20200310 MGI PMID:17167413 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20200310 MGI PMID:19246514 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20200310 MGI PMID:19246514 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200310 MGI PMID:19246514 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20200310 MGI PMID:16985211 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20200310 MGI PMID:16985211 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0003978 decreased circulating carnitine level IAGP N RGD:5509061 20200310 MGI PMID:19246514 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20200310 MGI PMID:19246514 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20200310 MGI PMID:19246514 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0005633 increased circulating sodium level IAGP N RGD:5509061 20200310 MGI PMID:16985211 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20200310 MGI PMID:16985211 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0008055 increased urine osmolality IAGP N RGD:5509061 20200310 MGI PMID:17167413 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20200310 MGI PMID:19246514 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0009645 crystalluria IAGP N RGD:5509061 20200310 MGI PMID:16985211 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20200310 MGI PMID:19246514 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0011417 abnormal renal transport IAGP N RGD:5509061 20200310 MGI PMID:17167413 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0011467 decreased urine urea nitrogen level IAGP N RGD:5509061 20200310 MGI PMID:16985211 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0013723 increased circulating tyrosine level IAGP N RGD:5509061 20200310 MGI PMID:16985211 1623240 Cltrn collectrin, amino acid transport regulator gene MP:0030644 increased circulating methionine level IAGP N RGD:5509061 20200310 MGI PMID:16985211 1623241 Psors1c2 psoriasis susceptibility 1 candidate 2 (human) gene MP:0005333 decreased heart rate IEA N RGD:5509061 20230601 MGI 1623241 Psors1c2 psoriasis susceptibility 1 candidate 2 (human) gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20230601 MGI 1623241 Psors1c2 psoriasis susceptibility 1 candidate 2 (human) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 1623242 Akip1 A kinase interacting protein 1 gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20220811 MGI PMID:35474062 1623242 Akip1 A kinase interacting protein 1 gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20220811 MGI PMID:35474062 1623242 Akip1 A kinase interacting protein 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20220811 MGI PMID:35474062 1623242 Akip1 A kinase interacting protein 1 gene MP:0012355 decreased prothrombin time IAGP N RGD:5509061 20220811 MGI PMID:35474062 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160804 MGI 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20160804 MGI 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0010571 shortened ST segment IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0010634 increased QRS amplitude IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0011928 abnormal mitral valve flow IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623244 Srsf4 serine and arginine-rich splicing factor 4 gene MP:0031609 increased fetal cardiomyocyte size IAGP N RGD:5509061 20240321 MGI PMID:34333993 1623245 Nelfcd negative elongation factor complex member C/D, Th1l gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1623245 Nelfcd negative elongation factor complex member C/D, Th1l gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 1623245 Nelfcd negative elongation factor complex member C/D, Th1l gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1623246 Plac1 placental specific protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22729990 1623246 Plac1 placental specific protein 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:22729990 1623246 Plac1 placental specific protein 1 gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:22729990 1623246 Plac1 placental specific protein 1 gene MP:0004260 enlarged placenta IAGP N RGD:5509061 20141003 MGI PMID:22729990 1623246 Plac1 placental specific protein 1 gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:22729990 1623246 Plac1 placental specific protein 1 gene MP:0008957 abnormal placenta junctional zone morphology IAGP N RGD:5509061 20141003 MGI PMID:22729990 1623246 Plac1 placental specific protein 1 gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:22729990 1623246 Plac1 placental specific protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22729990 1623246 Plac1 placental specific protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22729990 1623246 Plac1 placental specific protein 1 gene MP:0012098 increased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:22729990 1623247 Car5b carbonic anhydrase 5b, mitochondrial gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23589845 1623247 Car5b carbonic anhydrase 5b, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23589845 1623247 Car5b carbonic anhydrase 5b, mitochondrial gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22109883 1623247 Car5b carbonic anhydrase 5b, mitochondrial gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:23589845 1623247 Car5b carbonic anhydrase 5b, mitochondrial gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23589845 1623247 Car5b carbonic anhydrase 5b, mitochondrial gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23589845 1623248 Dgke diacylglycerol kinase, epsilon gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20181227 MGI 1623248 Dgke diacylglycerol kinase, epsilon gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20181227 MGI 1623248 Dgke diacylglycerol kinase, epsilon gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 1623248 Dgke diacylglycerol kinase, epsilon gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11287665 1623248 Dgke diacylglycerol kinase, epsilon gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:11287665 1623248 Dgke diacylglycerol kinase, epsilon gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20181227 MGI 1623249 Pdss1 prenyl (solanesyl) diphosphate synthase, subunit 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 1623249 Pdss1 prenyl (solanesyl) diphosphate synthase, subunit 1 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210128 MGI 1623249 Pdss1 prenyl (solanesyl) diphosphate synthase, subunit 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 1623249 Pdss1 prenyl (solanesyl) diphosphate synthase, subunit 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1623249 Pdss1 prenyl (solanesyl) diphosphate synthase, subunit 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1623249 Pdss1 prenyl (solanesyl) diphosphate synthase, subunit 1 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210128 MGI 1623249 Pdss1 prenyl (solanesyl) diphosphate synthase, subunit 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623249 Pdss1 prenyl (solanesyl) diphosphate synthase, subunit 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 1623249 Pdss1 prenyl (solanesyl) diphosphate synthase, subunit 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1623252 Bysl bystin-like gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1623252 Bysl bystin-like gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1623252 Bysl bystin-like gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1623252 Bysl bystin-like gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1623252 Bysl bystin-like gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17055491 1623252 Bysl bystin-like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1623252 Bysl bystin-like gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20181227 MGI 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20221215 MGI 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0001488 increased startle reflex IEA N RGD:5509061 20231207 MGI 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0002083 premature death IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0003354 astrocytosis IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20201022 MGI 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20240523 MGI 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20181227 MGI 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0008918 microgliosis IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20181227 MGI 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0010943 abnormal bronchus epithelium morphology IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0011475 abnormal glycosaminoglycan level IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20161117 MGI PMID:27491071 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20181227 MGI 1623253 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase gene MP:0014331 abnormal Purkinje cell mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:27491071 1623254 Spast spastin gene MP:0001147 small testis IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200402 MGI PMID:27019090 1623254 Spast spastin gene MP:0001405 impaired coordination IEA N RGD:5509061 20200310 MGI 1623254 Spast spastin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:17101632 1623254 Spast spastin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:19453301 1623254 Spast spastin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200402 MGI PMID:27019090 1623254 Spast spastin gene MP:0001407 short stride length IAGP N RGD:5509061 20200310 MGI PMID:17101632 1623254 Spast spastin gene MP:0001891 hydrocephaly IEA N RGD:5509061 20210128 MGI 1623254 Spast spastin gene MP:0001924 infertility IAGP N RGD:5509061 20200310 MGI PMID:17101632 1623254 Spast spastin gene MP:0001925 male infertility IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210128 MGI 1623254 Spast spastin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:17101632 1623254 Spast spastin gene MP:0004024 aneuploidy IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20200310 MGI PMID:19453301 1623254 Spast spastin gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0005159 azoospermia IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200310 MGI PMID:17101632 1623254 Spast spastin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200310 MGI PMID:19453301 1623254 Spast spastin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200402 MGI PMID:27019090 1623254 Spast spastin gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0010540 long stride length IAGP N RGD:5509061 20200402 MGI PMID:27019090 1623254 Spast spastin gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0031374 abnormal manchette assembly IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0031375 abnormal manchette disassembly IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623254 Spast spastin gene MP:0031386 elongated manchette IAGP N RGD:5509061 20230504 MGI PMID:36971361 1623257 Rnf17 ring finger protein 17 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16093322 1623257 Rnf17 ring finger protein 17 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:16093322 1623257 Rnf17 ring finger protein 17 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16093322 1623257 Rnf17 ring finger protein 17 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16093322 1623257 Rnf17 ring finger protein 17 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:16093322 1623257 Rnf17 ring finger protein 17 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20230420 MGI PMID:36930220 1623258 Reg3d regenerating islet-derived 3 delta gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 1623260 Dnajc12 DnaJ heat shock protein family (Hsp40) member C12 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 1623260 Dnajc12 DnaJ heat shock protein family (Hsp40) member C12 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12576554 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0002698 abnormal sclera morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0003622 ischuria IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0004287 abnormal spiral limbus morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0004288 abnormal spiral ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0004408 decreased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0006021 abnormal Reissner membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0008847 abnormal suprachiasmatic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0009945 abnormal accessory olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0009979 abnormal cerebellum deep nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:10588735 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:17712420 1623263 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) gene MP:0020475 delayed circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:17712420 1623264 Pdhx pyruvate dehydrogenase complex, component X gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20181227 MGI 1623264 Pdhx pyruvate dehydrogenase complex, component X gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1623264 Pdhx pyruvate dehydrogenase complex, component X gene MP:0001304 cataract IEA N RGD:5509061 20191128 MGI 1623264 Pdhx pyruvate dehydrogenase complex, component X gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1623264 Pdhx pyruvate dehydrogenase complex, component X gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 1623264 Pdhx pyruvate dehydrogenase complex, component X gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20181227 MGI 1623264 Pdhx pyruvate dehydrogenase complex, component X gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 1623264 Pdhx pyruvate dehydrogenase complex, component X gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623264 Pdhx pyruvate dehydrogenase complex, component X gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 1623266 Uty ubiquitously transcribed tetratricopeptide repeat containing, Y-linked gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23028370 1623266 Uty ubiquitously transcribed tetratricopeptide repeat containing, Y-linked gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:23028370 1623266 Uty ubiquitously transcribed tetratricopeptide repeat containing, Y-linked gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:23028370 1623266 Uty ubiquitously transcribed tetratricopeptide repeat containing, Y-linked gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23028370 1623266 Uty ubiquitously transcribed tetratricopeptide repeat containing, Y-linked gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:23028370 1623266 Uty ubiquitously transcribed tetratricopeptide repeat containing, Y-linked gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:23028370 1623266 Uty ubiquitously transcribed tetratricopeptide repeat containing, Y-linked gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23028370 1623266 Uty ubiquitously transcribed tetratricopeptide repeat containing, Y-linked gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:23028370 1623266 Uty ubiquitously transcribed tetratricopeptide repeat containing, Y-linked gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23028370 1623267 Utf1 undifferentiated embryonic cell transcription factor 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23874519 1623267 Utf1 undifferentiated embryonic cell transcription factor 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23874519 1623267 Utf1 undifferentiated embryonic cell transcription factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23874519 1623267 Utf1 undifferentiated embryonic cell transcription factor 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:23874519 1623267 Utf1 undifferentiated embryonic cell transcription factor 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:23874519 1623267 Utf1 undifferentiated embryonic cell transcription factor 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23874519 1623267 Utf1 undifferentiated embryonic cell transcription factor 1 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:23874519 1623267 Utf1 undifferentiated embryonic cell transcription factor 1 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:23874519 1623267 Utf1 undifferentiated embryonic cell transcription factor 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:23874519 1623267 Utf1 undifferentiated embryonic cell transcription factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23874519 1623267 Utf1 undifferentiated embryonic cell transcription factor 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23874519 1623268 Upk2 uroplakin 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:15611339 1623268 Upk2 uroplakin 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15611339 1623268 Upk2 uroplakin 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:15611339 1623268 Upk2 uroplakin 2 gene MP:0003587 ureter obstruction IAGP N RGD:5509061 20141003 MGI PMID:15611339 1623268 Upk2 uroplakin 2 gene MP:0003630 abnormal urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15611339 1623268 Upk2 uroplakin 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:15611339 1623268 Upk2 uroplakin 2 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:15611339 1623268 Upk2 uroplakin 2 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:15611339 1623268 Upk2 uroplakin 2 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15611339 1623268 Upk2 uroplakin 2 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:15611339 1623268 Upk2 uroplakin 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15611339 1623268 Upk2 uroplakin 2 gene MP:0011424 decreased urine uric acid level IAGP N RGD:5509061 20141003 MGI PMID:15611339 1623268 Upk2 uroplakin 2 gene MP:0011460 decreased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:15611339 1623268 Upk2 uroplakin 2 gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:15611339 1623269 Upk1b uroplakin 1B gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11689692 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11689692 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12882367 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11689692 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12882367 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:12882367 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11689692 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:16311597 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:16311597 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0002802 abnormal discrimination learning IAGP N RGD:5509061 20141003 MGI PMID:12882367 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0003335 exocrine pancreatic insufficiency IAGP N RGD:5509061 20141003 MGI PMID:16311597 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0003999 enhanced passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:16311597 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:11689692 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:11689692 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:11689692 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:11689692 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11689692 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623272 Ubr1 ubiquitin protein ligase E3 component n-recognin 1 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:16606826 1623280 Med22 mediator complex subunit 22 gene MP:0002083 premature death IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623280 Med22 mediator complex subunit 22 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623280 Med22 mediator complex subunit 22 gene MP:0002871 albuminuria IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623280 Med22 mediator complex subunit 22 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623280 Med22 mediator complex subunit 22 gene MP:0003606 kidney failure IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623280 Med22 mediator complex subunit 22 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623280 Med22 mediator complex subunit 22 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623280 Med22 mediator complex subunit 22 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623280 Med22 mediator complex subunit 22 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623280 Med22 mediator complex subunit 22 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623280 Med22 mediator complex subunit 22 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623280 Med22 mediator complex subunit 22 gene MP:0011282 increased podocyte apoptosis IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623280 Med22 mediator complex subunit 22 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623280 Med22 mediator complex subunit 22 gene MP:0011402 renal cast IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623280 Med22 mediator complex subunit 22 gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623280 Med22 mediator complex subunit 22 gene MP:0011899 podocyte vacuoles IAGP N RGD:5509061 20210325 MGI PMID:33208756 1623282 Supt4a SPT4A, DSIF elongation factor subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160505 MGI PMID:25760041 1623282 Supt4a SPT4A, DSIF elongation factor subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160505 MGI PMID:25760041 1623282 Supt4a SPT4A, DSIF elongation factor subunit gene MP:0002083 premature death IAGP N RGD:5509061 20160505 MGI PMID:25760041 1623282 Supt4a SPT4A, DSIF elongation factor subunit gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20181227 MGI 1623282 Supt4a SPT4A, DSIF elongation factor subunit gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20160505 MGI PMID:25760041 1623282 Supt4a SPT4A, DSIF elongation factor subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 1623282 Supt4a SPT4A, DSIF elongation factor subunit gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1623282 Supt4a SPT4A, DSIF elongation factor subunit gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1623283 Reg2 regenerating islet-derived 2 gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18678917 1623283 Reg2 regenerating islet-derived 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:18678917 1623283 Reg2 regenerating islet-derived 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18678917 1623283 Reg2 regenerating islet-derived 2 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17133485 1623283 Reg2 regenerating islet-derived 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 1623283 Reg2 regenerating islet-derived 2 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:17133485 1623283 Reg2 regenerating islet-derived 2 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:17133485 1623283 Reg2 regenerating islet-derived 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17133485 1623283 Reg2 regenerating islet-derived 2 gene MP:0031324 delayed liver regeneration IAGP N RGD:5509061 20220106 MGI PMID:17133485 1623284 Rdh16 retinol dehydrogenase 16 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20160804 MGI 1623288 Rbpms RNA binding protein gene with multiple splicing gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20220630 MGI PMID:35472321 1623288 Rbpms RNA binding protein gene with multiple splicing gene MP:0001575 cyanosis IAGP N RGD:5509061 20220630 MGI PMID:35472321 1623288 Rbpms RNA binding protein gene with multiple splicing gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 1623288 Rbpms RNA binding protein gene with multiple splicing gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20220630 MGI PMID:35472321 1623288 Rbpms RNA binding protein gene with multiple splicing gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20220630 MGI PMID:35472321 1623288 Rbpms RNA binding protein gene with multiple splicing gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20220630 MGI PMID:35472321 1623288 Rbpms RNA binding protein gene with multiple splicing gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20220630 MGI PMID:35472321 1623288 Rbpms RNA binding protein gene with multiple splicing gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20220630 MGI PMID:35472321 1623288 Rbpms RNA binding protein gene with multiple splicing gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20220630 MGI PMID:35472321 1623288 Rbpms RNA binding protein gene with multiple splicing gene MP:0010909 pulmonary alveolar hemorrhage IAGP N RGD:5509061 20220630 MGI PMID:35472321 1623288 Rbpms RNA binding protein gene with multiple splicing gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20220630 MGI PMID:35472321 1623288 Rbpms RNA binding protein gene with multiple splicing gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 1623288 Rbpms RNA binding protein gene with multiple splicing gene MP:0014519 myocardial ventricular hypertrabeculation IAGP N RGD:5509061 20240822 MGI PMID:35472321 1623288 Rbpms RNA binding protein gene with multiple splicing gene MP:0031611 decreased fetal cardiomyocyte number IAGP N RGD:5509061 20240404 MGI PMID:35472321 1623303 Ly96 lymphocyte antigen 96 gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12055629 1623303 Ly96 lymphocyte antigen 96 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12055629 1623303 Ly96 lymphocyte antigen 96 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12055629 1623303 Ly96 lymphocyte antigen 96 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12055629 1623303 Ly96 lymphocyte antigen 96 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:12055629 1623303 Ly96 lymphocyte antigen 96 gene MP:0008658 decreased interleukin-1 beta secretion IEA N RGD:5509061 20181011 MGI 1623303 Ly96 lymphocyte antigen 96 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:12055629 1623303 Ly96 lymphocyte antigen 96 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:15369778 1623303 Ly96 lymphocyte antigen 96 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12055629 1623303 Ly96 lymphocyte antigen 96 gene MP:0011081 decreased macrophage apoptosis IEA N RGD:5509061 20181011 MGI 1623309 Gbp2b guanylate binding protein 2b gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21551061 1623309 Gbp2b guanylate binding protein 2b gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21551061 1623309 Gbp2b guanylate binding protein 2b gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:21551061 1623309 Gbp2b guanylate binding protein 2b gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:21551061 1623309 Gbp2b guanylate binding protein 2b gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21551061 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:16954197 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17079175 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:16954197 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:16954197 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:14578207 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:14578207 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:16954197 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17079175 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16954197 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:17079175 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:9482915 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001190 reddish skin IAGP N RGD:5509061 20230608 MGI PMID:35711931 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:14578207 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:14578207 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:17079175 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:9482915 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20230608 MGI PMID:35711931 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20230608 MGI PMID:35711931 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20230608 MGI PMID:35711931 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20230608 MGI PMID:35711931 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:9482915 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230608 MGI PMID:35711931 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:9482915 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:17079175 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:1594045 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001577 anemia IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:1594045 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:1594045 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:21700325 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002295 abnormal pulmonary circulation IAGP N RGD:5509061 20141003 MGI PMID:14578207 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:16954197 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:17079175 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:1594045 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:17079175 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:16954197 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:1594045 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:16954197 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:16954197 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:21700325 1623310 Gba1 glucosylceramidase beta 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141030 MGI PMID:24388731 1623310 Gba1 glucosylceramidase beta 1 gene MP:0003652 abnormal skin turgor IAGP N RGD:5509061 20230608 MGI PMID:35711931 1623310 Gba1 glucosylceramidase beta 1 gene MP:0003653 decreased skin turgor IAGP N RGD:5509061 20141003 MGI PMID:9482915 1623310 Gba1 glucosylceramidase beta 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:14578207 1623310 Gba1 glucosylceramidase beta 1 gene MP:0003865 lymph node inflammation IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141030 MGI PMID:24388731 1623310 Gba1 glucosylceramidase beta 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17079175 1623310 Gba1 glucosylceramidase beta 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:7753840 1623310 Gba1 glucosylceramidase beta 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:1594045 1623310 Gba1 glucosylceramidase beta 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16954197 1623310 Gba1 glucosylceramidase beta 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17079175 1623310 Gba1 glucosylceramidase beta 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141030 MGI PMID:24388731 1623310 Gba1 glucosylceramidase beta 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:16954197 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:16954197 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20141030 MGI PMID:24388731 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008599 increased circulating interleukin-2 level IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008608 increased circulating interleukin-13 level IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008623 increased circulating interleukin-3 level IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008629 increased circulating interleukin-9 level IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008639 decreased circulating interleukin-1 alpha level IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008737 abnormal spleen physiology IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20231207 MGI 1623310 Gba1 glucosylceramidase beta 1 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:9482915 1623310 Gba1 glucosylceramidase beta 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:1594045 1623310 Gba1 glucosylceramidase beta 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:9482915 1623310 Gba1 glucosylceramidase beta 1 gene MP:0009974 decreased cerebral cortex pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:20962279 1623310 Gba1 glucosylceramidase beta 1 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20231207 MGI 1623310 Gba1 glucosylceramidase beta 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9482915 1623310 Gba1 glucosylceramidase beta 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20230608 MGI PMID:35711931 1623310 Gba1 glucosylceramidase beta 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20181108 MGI PMID:11994410 1623310 Gba1 glucosylceramidase beta 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16954197 1623310 Gba1 glucosylceramidase beta 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17079175 1623310 Gba1 glucosylceramidase beta 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17954912 1623310 Gba1 glucosylceramidase beta 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7753840 1623310 Gba1 glucosylceramidase beta 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14578207 1623310 Gba1 glucosylceramidase beta 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7753840 1623310 Gba1 glucosylceramidase beta 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1623310 Gba1 glucosylceramidase beta 1 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:20962279 1623311 Gas1 growth arrest specific 1 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20171026 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230420 MGI PMID:27811357 1623311 Gas1 growth arrest specific 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17504940 1623311 Gas1 growth arrest specific 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:17504940 1623311 Gas1 growth arrest specific 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17504940 1623311 Gas1 growth arrest specific 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:17504940 1623311 Gas1 growth arrest specific 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:12399319 1623311 Gas1 growth arrest specific 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:17504940 1623311 Gas1 growth arrest specific 1 gene MP:0000566 synostosis IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:11456442 1623311 Gas1 growth arrest specific 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:11456442 1623311 Gas1 growth arrest specific 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:11456442 1623311 Gas1 growth arrest specific 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11456442 1623311 Gas1 growth arrest specific 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:11456442 1623311 Gas1 growth arrest specific 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11456442 1623311 Gas1 growth arrest specific 1 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:11456442 1623311 Gas1 growth arrest specific 1 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17504940 1623311 Gas1 growth arrest specific 1 gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11456442 1623311 Gas1 growth arrest specific 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11456442 1623311 Gas1 growth arrest specific 1 gene MP:0001679 thin apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:12399319 1623311 Gas1 growth arrest specific 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17504940 1623311 Gas1 growth arrest specific 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17504940 1623311 Gas1 growth arrest specific 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17504940 1623311 Gas1 growth arrest specific 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:17504940 1623311 Gas1 growth arrest specific 1 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12399319 1623311 Gas1 growth arrest specific 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0002243 abnormal vomeronasal organ morphology IAGP N RGD:5509061 20230420 MGI PMID:27811357 1623311 Gas1 growth arrest specific 1 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:12399319 1623311 Gas1 growth arrest specific 1 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:12399319 1623311 Gas1 growth arrest specific 1 gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:17504940 1623311 Gas1 growth arrest specific 1 gene MP:0004053 abnormal synchondrosis IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0004318 absent incus IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0004319 absent malleus IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0004459 small alisphenoid bone IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0004460 alisphenoid bone hypoplasia IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0004539 absent maxilla IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:12399319 1623311 Gas1 growth arrest specific 1 gene MP:0004635 short metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:12399319 1623311 Gas1 growth arrest specific 1 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0004790 absent upper incisors IAGP N RGD:5509061 20221215 MGI PMID:28771384 1623311 Gas1 growth arrest specific 1 gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:17504940 1623311 Gas1 growth arrest specific 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20230420 MGI PMID:27811357 1623311 Gas1 growth arrest specific 1 gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20150528 MGI PMID:11456442 1623311 Gas1 growth arrest specific 1 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0005195 abnormal posterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:12399319 1623311 Gas1 growth arrest specific 1 gene MP:0005352 small cranium IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:12399319 1623311 Gas1 growth arrest specific 1 gene MP:0006033 abnormal external auditory canal morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:11456442 1623311 Gas1 growth arrest specific 1 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20150528 MGI PMID:12399319 1623311 Gas1 growth arrest specific 1 gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0008374 abnormal malleus manubrium morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0008381 absent gonial bone IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0008382 gonial bone hypoplasia IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:11456442 1623311 Gas1 growth arrest specific 1 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20230420 MGI PMID:27811357 1623311 Gas1 growth arrest specific 1 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20230420 MGI PMID:27811357 1623311 Gas1 growth arrest specific 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20230420 MGI PMID:27811357 1623311 Gas1 growth arrest specific 1 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20171026 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0009909 bifid tongue IAGP N RGD:5509061 20230420 MGI PMID:27811357 1623311 Gas1 growth arrest specific 1 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0010324 abnormal malleus processus brevis morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0010327 abnormal malleus neck morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17504940 1623311 Gas1 growth arrest specific 1 gene MP:0011261 abnormal limb mesenchyme morphology IAGP N RGD:5509061 20150528 MGI PMID:12399319 1623311 Gas1 growth arrest specific 1 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20230810 MGI PMID:11456441 1623311 Gas1 growth arrest specific 1 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0012270 cardiac edema IAGP N RGD:5509061 20141003 MGI PMID:17504940 1623311 Gas1 growth arrest specific 1 gene MP:0013595 absent vomeronasal organ IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0013790 single external naris IAGP N RGD:5509061 20150611 MGI PMID:17504940 1623311 Gas1 growth arrest specific 1 gene MP:0013790 single external naris IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0013826 absent hypoglossal canal IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0014291 decreased autopod size IAGP N RGD:5509061 20230824 MGI PMID:12399319 1623311 Gas1 growth arrest specific 1 gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:11456442 1623311 Gas1 growth arrest specific 1 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230420 MGI PMID:27811357 1623311 Gas1 growth arrest specific 1 gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0030170 absent mandibular symphysis IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20171109 MGI PMID:17504941 1623311 Gas1 growth arrest specific 1 gene MP:0030321 abnormal tegmen tympani morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0030322 styloid process hypoplasia IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20221201 MGI PMID:17525797 1623311 Gas1 growth arrest specific 1 gene MP:0031499 decreased cornea size IAGP N RGD:5509061 20230810 MGI PMID:11456441 1623312 B4galnt2 beta-1,4-N-acetyl-galactosaminyl transferase 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1623312 B4galnt2 beta-1,4-N-acetyl-galactosaminyl transferase 2 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20150226 MGI PMID:23118208 1623312 B4galnt2 beta-1,4-N-acetyl-galactosaminyl transferase 2 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 1623312 B4galnt2 beta-1,4-N-acetyl-galactosaminyl transferase 2 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20150226 MGI PMID:23118208 1623312 B4galnt2 beta-1,4-N-acetyl-galactosaminyl transferase 2 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20150226 MGI PMID:23118208 1623312 B4galnt2 beta-1,4-N-acetyl-galactosaminyl transferase 2 gene MP:0014234 decreased enterocyte apoptosis IAGP N RGD:5509061 20230323 MGI PMID:10097137 1623314 Cd55b CD55 molecule, decay accelerating factor for complement B gene MP:0005505 thrombocytosis IEA N RGD:5509061 20160114 MGI 1623314 Cd55b CD55 molecule, decay accelerating factor for complement B gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1623314 Cd55b CD55 molecule, decay accelerating factor for complement B gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 1623315 Dach1 dachshund family transcription factor 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:11238885 1623315 Dach1 dachshund family transcription factor 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210826 MGI 1623315 Dach1 dachshund family transcription factor 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11238885 1623315 Dach1 dachshund family transcription factor 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12508235 1623315 Dach1 dachshund family transcription factor 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11238885 1623315 Dach1 dachshund family transcription factor 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12508235 1623315 Dach1 dachshund family transcription factor 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1623315 Dach1 dachshund family transcription factor 1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20160421 MGI 1623315 Dach1 dachshund family transcription factor 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:20869363 1623315 Dach1 dachshund family transcription factor 1 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:20869363 1623315 Dach1 dachshund family transcription factor 1 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:20869363 1623315 Dach1 dachshund family transcription factor 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:12508235 1623315 Dach1 dachshund family transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11238885 1623315 Dach1 dachshund family transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12508235 1623315 Dach1 dachshund family transcription factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623315 Dach1 dachshund family transcription factor 1 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20150611 MGI PMID:20869363 1623318 Cyp2j5 cytochrome P450, family 2, subfamily j, polypeptide 5 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18716027 1623318 Cyp2j5 cytochrome P450, family 2, subfamily j, polypeptide 5 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:18716027 1623318 Cyp2j5 cytochrome P450, family 2, subfamily j, polypeptide 5 gene MP:0003371 decreased circulating estrogen level IAGP N RGD:5509061 20141003 MGI PMID:18716027 1623318 Cyp2j5 cytochrome P450, family 2, subfamily j, polypeptide 5 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:18716027 1623318 Cyp2j5 cytochrome P450, family 2, subfamily j, polypeptide 5 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18716027 1623318 Cyp2j5 cytochrome P450, family 2, subfamily j, polypeptide 5 gene MP:0011417 abnormal renal transport IAGP N RGD:5509061 20141003 MGI PMID:18716027 1623320 Arhgap6 Rho GTPase activating protein 6 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:12444108 1623320 Arhgap6 Rho GTPase activating protein 6 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:12444108 1623320 Arhgap6 Rho GTPase activating protein 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10699171 1623320 Arhgap6 Rho GTPase activating protein 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12444108 1623320 Arhgap6 Rho GTPase activating protein 6 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12444108 1623320 Arhgap6 Rho GTPase activating protein 6 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12444108 1623348 Fignl2 fidgetin-like 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20210923 MGI PMID:33872220 1623348 Fignl2 fidgetin-like 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20210923 MGI PMID:33872220 1623348 Fignl2 fidgetin-like 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20210923 MGI PMID:33872220 1623348 Fignl2 fidgetin-like 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20210923 MGI PMID:33872220 1623351 Bin2 bridging integrator 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:32750041 1623351 Bin2 bridging integrator 2 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210520 MGI 1623351 Bin2 bridging integrator 2 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210520 MGI 1623351 Bin2 bridging integrator 2 gene MP:0004865 abnormal platelet calcium level IAGP N RGD:5509061 20210401 MGI PMID:32750041 1623351 Bin2 bridging integrator 2 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20210401 MGI PMID:32750041 1623351 Bin2 bridging integrator 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 1623351 Bin2 bridging integrator 2 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20210401 MGI PMID:32750041 1623351 Bin2 bridging integrator 2 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20210401 MGI PMID:32750041 1623351 Bin2 bridging integrator 2 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20210401 MGI PMID:32750041 1623351 Bin2 bridging integrator 2 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20210401 MGI PMID:32750041 1623351 Bin2 bridging integrator 2 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20201231 MGI 1623351 Bin2 bridging integrator 2 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20210401 MGI PMID:32750041 1623351 Bin2 bridging integrator 2 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20210401 MGI PMID:32750041 1623354 Efr3b EFR3 homolog B gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20220811 MGI 1623354 Efr3b EFR3 homolog B gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 1623354 Efr3b EFR3 homolog B gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 1623354 Efr3b EFR3 homolog B gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1623354 Efr3b EFR3 homolog B gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20240307 MGI PMID:38190534 1623354 Efr3b EFR3 homolog B gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20240307 MGI PMID:38190534 1623354 Efr3b EFR3 homolog B gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20220811 MGI 1623354 Efr3b EFR3 homolog B gene MP:0003960 increased lean body mass IEA N RGD:5509061 20190502 MGI 1623354 Efr3b EFR3 homolog B gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220811 MGI 1623354 Efr3b EFR3 homolog B gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 1623354 Efr3b EFR3 homolog B gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20211021 MGI 1623354 Efr3b EFR3 homolog B gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20240523 MGI 1623354 Efr3b EFR3 homolog B gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1623354 Efr3b EFR3 homolog B gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20190502 MGI 1623354 Efr3b EFR3 homolog B gene MP:0010052 increased grip strength IEA N RGD:5509061 20190502 MGI 1623354 Efr3b EFR3 homolog B gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20190502 MGI 1623354 Efr3b EFR3 homolog B gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20240307 MGI PMID:38190534 1623399 Ms4a4a membrane-spanning 4-domains, subfamily A, member 4A gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 1623399 Ms4a4a membrane-spanning 4-domains, subfamily A, member 4A gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1623399 Ms4a4a membrane-spanning 4-domains, subfamily A, member 4A gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20210617 MGI PMID:32589266 1623399 Ms4a4a membrane-spanning 4-domains, subfamily A, member 4A gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20210617 MGI PMID:32589266 1623399 Ms4a4a membrane-spanning 4-domains, subfamily A, member 4A gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20210617 MGI PMID:32589266 1623399 Ms4a4a membrane-spanning 4-domains, subfamily A, member 4A gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20210617 MGI PMID:32589266 1623399 Ms4a4a membrane-spanning 4-domains, subfamily A, member 4A gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20210617 MGI PMID:32589266 1623399 Ms4a4a membrane-spanning 4-domains, subfamily A, member 4A gene MP:0009453 enhanced contextual conditioning behavior IEA N RGD:5509061 20230601 MGI 1623455 Naaladl2 N-acetylated alpha-linked acidic dipeptidase-like 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20231207 MGI 1623455 Naaladl2 N-acetylated alpha-linked acidic dipeptidase-like 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 1623493 Gm6578 predicted gene 6578 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1623530 Mast3 microtubule associated serine/threonine kinase 3 gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 1623530 Mast3 microtubule associated serine/threonine kinase 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1623530 Mast3 microtubule associated serine/threonine kinase 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 1623533 Rps23rg1 ribosomal protein S23, retrogene 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20191017 MGI PMID:30292394 1623533 Rps23rg1 ribosomal protein S23, retrogene 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20191017 MGI PMID:30292394 1623533 Rps23rg1 ribosomal protein S23, retrogene 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20191017 MGI PMID:30292394 1623533 Rps23rg1 ribosomal protein S23, retrogene 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20191017 MGI PMID:30292394 1623533 Rps23rg1 ribosomal protein S23, retrogene 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20191017 MGI PMID:30292394 1623533 Rps23rg1 ribosomal protein S23, retrogene 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20191017 MGI PMID:30292394 1623533 Rps23rg1 ribosomal protein S23, retrogene 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20191017 MGI PMID:30292394 1623533 Rps23rg1 ribosomal protein S23, retrogene 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20191017 MGI PMID:30292394 1623533 Rps23rg1 ribosomal protein S23, retrogene 1 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20191017 MGI PMID:30292394 1623533 Rps23rg1 ribosomal protein S23, retrogene 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20191017 MGI PMID:30292394 1623533 Rps23rg1 ribosomal protein S23, retrogene 1 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20191017 MGI PMID:30292394 1623538 Srcap Snf2-related CREBBP activator protein gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20201022 MGI 1623538 Srcap Snf2-related CREBBP activator protein gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210128 MGI 1623538 Srcap Snf2-related CREBBP activator protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20210506 MGI PMID:32449550 1623538 Srcap Snf2-related CREBBP activator protein gene MP:0012128 abnormal blastocyst formation IAGP N RGD:5509061 20210506 MGI PMID:32449550 1623542 Tug1 taurine upregulated gene 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24381249 1623544 Uqcc6 ubiquinol-cytochrome c reductase complex assembly factor 6 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20230112 MGI PMID:35977508 1623544 Uqcc6 ubiquinol-cytochrome c reductase complex assembly factor 6 gene MP:0012735 abnormal response to exercise IAGP N RGD:5509061 20230112 MGI PMID:35977508 1623544 Uqcc6 ubiquinol-cytochrome c reductase complex assembly factor 6 gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20230112 MGI PMID:35977508 1623550 Adgrf2 adhesion G protein-coupled receptor F2 gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20231116 MGI PMID:36929047 1623559 Trim72 tripartite motif-containing 72 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:20139895 1623559 Trim72 tripartite motif-containing 72 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:19043407 1623559 Trim72 tripartite motif-containing 72 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19043407 1623559 Trim72 tripartite motif-containing 72 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:19043407 1623559 Trim72 tripartite motif-containing 72 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19043407 1623559 Trim72 tripartite motif-containing 72 gene MP:0002323 decreased susceptibility to hyperlipidemia IAGP N RGD:5509061 20240111 MGI PMID:34844991 1623559 Trim72 tripartite motif-containing 72 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19043407 1623559 Trim72 tripartite motif-containing 72 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20240111 MGI PMID:34844991 1623559 Trim72 tripartite motif-containing 72 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:19043407 1623559 Trim72 tripartite motif-containing 72 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:19043407 1623559 Trim72 tripartite motif-containing 72 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:20139895 1623559 Trim72 tripartite motif-containing 72 gene MP:0020090 decreased susceptibility to diet-induced non-insulin dependent diabetes IAGP N RGD:5509061 20240111 MGI PMID:34844991 1623559 Trim72 tripartite motif-containing 72 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240111 MGI PMID:34844991 1623564 Lrrc32 leucine rich repeat containing 32 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221013 MGI PMID:28912269 1623564 Lrrc32 leucine rich repeat containing 32 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23645881 1623564 Lrrc32 leucine rich repeat containing 32 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20221013 MGI PMID:28912269 1623564 Lrrc32 leucine rich repeat containing 32 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221013 MGI PMID:28912269 1623564 Lrrc32 leucine rich repeat containing 32 gene MP:0009889 persistence of medial edge epithelium during palatal shelf fusion IAGP N RGD:5509061 20221013 MGI PMID:28912269 1623564 Lrrc32 leucine rich repeat containing 32 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221013 MGI PMID:28912269 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20240704 MGI PMID:38598293 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0002871 albuminuria IAGP N RGD:5509061 20240704 MGI PMID:38598293 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20240704 MGI PMID:38598293 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20240704 MGI PMID:38598293 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20240704 MGI PMID:38598293 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20240704 MGI PMID:38598293 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20240704 MGI PMID:38598293 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20240704 MGI PMID:38598293 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0011350 abnormal proximal convoluted tubule brush border morphology IAGP N RGD:5509061 20240704 MGI PMID:38598293 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0020400 cystinuria IAGP N RGD:5509061 20240704 MGI PMID:38598293 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0020404 prolinuria IAGP N RGD:5509061 20240704 MGI PMID:38598293 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20240704 MGI PMID:38598293 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0020992 increased urine HAVCR1 level IAGP N RGD:5509061 20240704 MGI PMID:38598293 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0030617 hyperglutaminuria IAGP N RGD:5509061 20240704 MGI PMID:38598293 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20240704 MGI PMID:38598293 1623566 Whamm WAS protein homolog associated with actin, golgi membranes and microtubules gene MP:0031637 methioninuria IAGP N RGD:5509061 20240801 MGI PMID:38598293 1623567 Slc28a1 solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20240620 MGI PMID:37264059 1623567 Slc28a1 solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20240620 MGI PMID:37264059 1623567 Slc28a1 solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 gene MP:0001577 anemia IAGP N RGD:5509061 20240620 MGI PMID:37264059 1623567 Slc28a1 solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20240620 MGI PMID:37264059 1623567 Slc28a1 solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20240620 MGI PMID:37264059 1623567 Slc28a1 solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20240620 MGI PMID:37264059 1623567 Slc28a1 solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20240620 MGI PMID:37264059 1623567 Slc28a1 solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20240620 MGI PMID:37264059 1623567 Slc28a1 solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20240620 MGI PMID:37264059 1623567 Slc28a1 solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20240620 MGI PMID:37264059 1623567 Slc28a1 solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 gene MP:0011477 abnormal urine nucleoside level IAGP N RGD:5509061 20240620 MGI PMID:37264059 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:16354937 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20220407 MGI PMID:34625556 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16354937 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0001072 abnormal vestibulocochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16354937 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0001194 dermatitis IAGP N RGD:5509061 20220407 MGI PMID:34625556 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20220407 MGI PMID:34625556 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0001212 skin lesions IAGP N RGD:5509061 20220407 MGI PMID:34625556 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20220407 MGI PMID:34625556 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23708998 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16354937 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:16354937 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20220407 MGI PMID:34625556 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20220407 MGI PMID:34625556 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20220407 MGI PMID:34625556 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:23708998 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20220407 MGI PMID:34625556 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23708998 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:23708998 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20220407 MGI PMID:34625556 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0009793 sebaceous gland hypertrophy IAGP N RGD:5509061 20220407 MGI PMID:34625556 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0011006 abnormal epidermal stem cell proliferation IAGP N RGD:5509061 20220407 MGI PMID:34625556 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0011007 abnormal epidermal stem cell apoptosis IAGP N RGD:5509061 20220407 MGI PMID:34625556 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20220407 MGI PMID:34625556 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23708998 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0012730 abnormal internal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23708998 1623582 Otulin OTU deubiquitinase with linear linkage specificity gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1623585 Zfp950 zinc finger protein 950 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0000097 short maxilla IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0000111 cleft palate IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0000480 increased rib number IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0000767 abnormal smooth muscle morphology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0001255 decreased body height IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0002989 small kidney IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0004969 pale kidney IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0009895 decreased palatine bone horizontal plate size IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0030189 broad snout IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623585 Zfp950 zinc finger protein 950 gene MP:0030383 small presphenoid bone IAGP N RGD:5509061 20200310 MGI PMID:17143286 1623660 Kif28 kinesin family member 28 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1623661 Gpr25 G protein-coupled receptor 25 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1623661 Gpr25 G protein-coupled receptor 25 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24838000 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:23236174 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23236174 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23236174 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:24838000 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23236174 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:23236174 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:23236174 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:24838000 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:24838000 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23236174 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:24838000 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:24838000 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:24838000 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0009357 abnormal seizure response to inducing agent IAGP N RGD:5509061 20141003 MGI PMID:24838000 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23236174 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23236174 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20230601 MGI 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20141003 MGI PMID:24838000 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0012444 thin hippocampus molecular cell layer IAGP N RGD:5509061 20141003 MGI PMID:24838000 1623666 Cdkl5 cyclin dependent kinase like 5 gene MP:0012446 thin hippocampus stratum oriens IAGP N RGD:5509061 20141003 MGI PMID:24838000 1623667 Bclaf3 Bclaf1 and Thrap3 family member 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1623671 Brwd3 bromodomain and WD repeat domain containing 3 gene MP:0000433 microcephaly IEA N RGD:5509061 20111116 MGI 1623671 Brwd3 bromodomain and WD repeat domain containing 3 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20111116 MGI 1623671 Brwd3 bromodomain and WD repeat domain containing 3 gene MP:0012062 small tail bud IEA N RGD:5509061 20141003 MGI 1623675 Gm1140 predicted gene 1140 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201224 MGI PMID:32493902 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0001726 abnormal allantois morphology IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0001785 edema IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:12955145 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:24303013 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24303013 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:24303013 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:24303013 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0004413 absent cochlear microphonics IAGP N RGD:5509061 20141003 MGI PMID:24303013 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:24303013 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0005533 increased body temperature IEA N RGD:5509061 20210128 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0008854 bleb IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0009806 abnormal otic vesicle morphology IEA N RGD:5509061 20210826 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:24303013 1623681 Alg10b ALG10 alpha-1,2-glucosyltransferase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210826 MGI 1623683 Olfm4 olfactomedin 4 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:20534456 1623683 Olfm4 olfactomedin 4 gene MP:0002083 premature death IAGP N RGD:5509061 20191003 MGI PMID:30842416 1623683 Olfm4 olfactomedin 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20534456 1623683 Olfm4 olfactomedin 4 gene MP:0005381 digestive/alimentary phenotype IAGP N RGD:5509061 20200409 MGI PMID:30449703 1623683 Olfm4 olfactomedin 4 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:20534456 1623683 Olfm4 olfactomedin 4 gene MP:0008623 increased circulating interleukin-3 level IAGP N RGD:5509061 20141003 MGI PMID:20534456 1623683 Olfm4 olfactomedin 4 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:20534456 1623683 Olfm4 olfactomedin 4 gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20191003 MGI PMID:30842416 1623683 Olfm4 olfactomedin 4 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20141003 MGI PMID:20534456 1623683 Olfm4 olfactomedin 4 gene MP:0014201 abnormal intestinal epithelium physiology IAGP N RGD:5509061 20200409 MGI PMID:30449703 1623684 Dgkh diacylglycerol kinase, eta gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20220714 MGI PMID:30985063 1623684 Dgkh diacylglycerol kinase, eta gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20220714 MGI PMID:27167678 1623684 Dgkh diacylglycerol kinase, eta gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20220714 MGI PMID:30985063 1623684 Dgkh diacylglycerol kinase, eta gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20220714 MGI PMID:30985063 1623684 Dgkh diacylglycerol kinase, eta gene MP:0001399 hyperactivity IAGP N RGD:5509061 20220714 MGI PMID:27167678 1623684 Dgkh diacylglycerol kinase, eta gene MP:0001399 hyperactivity IAGP N RGD:5509061 20220714 MGI PMID:30985063 1623684 Dgkh diacylglycerol kinase, eta gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20220714 MGI PMID:30985063 1623684 Dgkh diacylglycerol kinase, eta gene MP:0003063 increased coping response IAGP N RGD:5509061 20220714 MGI PMID:27167678 1623684 Dgkh diacylglycerol kinase, eta gene MP:0003063 increased coping response IAGP N RGD:5509061 20220714 MGI PMID:30985063 1623684 Dgkh diacylglycerol kinase, eta gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1623684 Dgkh diacylglycerol kinase, eta gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20220811 MGI 1623684 Dgkh diacylglycerol kinase, eta gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20220714 MGI PMID:27167678 1623684 Dgkh diacylglycerol kinase, eta gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20220714 MGI PMID:27167678 1623684 Dgkh diacylglycerol kinase, eta gene MP:0020379 abnormal sucrose solution preference IAGP N RGD:5509061 20220714 MGI PMID:30985063 1623695 Xkrx X-linked Kx blood group related, X-linked gene MP:0004794 increased anti-nuclear antigen antibody level IEA N RGD:5509061 20201022 MGI 1623697 Garin1b golgi associated RAB2 interactor 1B gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 1623697 Garin1b golgi associated RAB2 interactor 1B gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 1623697 Garin1b golgi associated RAB2 interactor 1B gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 1623697 Garin1b golgi associated RAB2 interactor 1B gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 1623697 Garin1b golgi associated RAB2 interactor 1B gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 1623697 Garin1b golgi associated RAB2 interactor 1B gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 1623697 Garin1b golgi associated RAB2 interactor 1B gene MP:0001925 male infertility IAGP N RGD:5509061 20211209 MGI PMID:34714330 1623697 Garin1b golgi associated RAB2 interactor 1B gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 1623697 Garin1b golgi associated RAB2 interactor 1B gene MP:0003604 single kidney IEA N RGD:5509061 20230601 MGI 1623697 Garin1b golgi associated RAB2 interactor 1B gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20211209 MGI PMID:34714330 1623697 Garin1b golgi associated RAB2 interactor 1B gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20230601 MGI 1623697 Garin1b golgi associated RAB2 interactor 1B gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20211209 MGI PMID:34714330 1623697 Garin1b golgi associated RAB2 interactor 1B gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20211209 MGI PMID:34714330 1623697 Garin1b golgi associated RAB2 interactor 1B gene MP:0009280 decreased activated sperm motility IAGP N RGD:5509061 20211209 MGI PMID:34714330 1623697 Garin1b golgi associated RAB2 interactor 1B gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20211209 MGI PMID:34714330 1623698 Thsd7a thrombospondin, type I, domain containing 7A gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1623698 Thsd7a thrombospondin, type I, domain containing 7A gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 1623698 Thsd7a thrombospondin, type I, domain containing 7A gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1623698 Thsd7a thrombospondin, type I, domain containing 7A gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1623698 Thsd7a thrombospondin, type I, domain containing 7A gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1623698 Thsd7a thrombospondin, type I, domain containing 7A gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 1623700 Spdye4b speedy/RINGO cell cycle regulator family, member E4B gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20160811 MGI 1623701 Sdk1 sidekick cell adhesion molecule 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 1623705 Mcc mutated in colorectal cancers gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22016184 1623705 Mcc mutated in colorectal cancers gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20201001 MGI PMID:30831321 1623705 Mcc mutated in colorectal cancers gene MP:0009310 increased large intestine adenocarcinoma incidence IAGP N RGD:5509061 20201002 MGI PMID:30831321 1623715 Wnk3 WNK lysine deficient protein kinase 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 1623715 Wnk3 WNK lysine deficient protein kinase 3 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20190815 MGI PMID:23213404 1623719 Rasl10b RAS-like, family 10, member B gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20200310 MGI PMID:17984325 1623719 Rasl10b RAS-like, family 10, member B gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20200310 MGI PMID:17984325 1623720 Ccdc42 coiled-coil domain containing 42 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20170119 MGI PMID:26945718 1623720 Ccdc42 coiled-coil domain containing 42 gene MP:0001925 male infertility IAGP N RGD:5509061 20170119 MGI PMID:26945718 1623720 Ccdc42 coiled-coil domain containing 42 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20170119 MGI PMID:26945718 1623720 Ccdc42 coiled-coil domain containing 42 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20170119 MGI PMID:26945718 1623720 Ccdc42 coiled-coil domain containing 42 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20170119 MGI PMID:26945718 1623720 Ccdc42 coiled-coil domain containing 42 gene MP:0005159 azoospermia IAGP N RGD:5509061 20170119 MGI PMID:26945718 1623720 Ccdc42 coiled-coil domain containing 42 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20170119 MGI PMID:26945718 1623720 Ccdc42 coiled-coil domain containing 42 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20170119 MGI PMID:26945718 1623720 Ccdc42 coiled-coil domain containing 42 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20170119 MGI PMID:26945718 1623720 Ccdc42 coiled-coil domain containing 42 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20170119 MGI PMID:26945718 1623720 Ccdc42 coiled-coil domain containing 42 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20170119 MGI PMID:26945718 1623720 Ccdc42 coiled-coil domain containing 42 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20170119 MGI PMID:26945718 1623720 Ccdc42 coiled-coil domain containing 42 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20170119 MGI PMID:26945718 1623720 Ccdc42 coiled-coil domain containing 42 gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20170119 MGI PMID:26945718 1623720 Ccdc42 coiled-coil domain containing 42 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20170119 MGI PMID:26945718 1623721 Gemin4 gem nuclear organelle associated protein 4 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20201022 MGI 1623721 Gemin4 gem nuclear organelle associated protein 4 gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20201231 MGI 1623721 Gemin4 gem nuclear organelle associated protein 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 1623721 Gemin4 gem nuclear organelle associated protein 4 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 1623721 Gemin4 gem nuclear organelle associated protein 4 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 1623721 Gemin4 gem nuclear organelle associated protein 4 gene MP:0009850 embryonic lethality between implantation and placentation IAGP N RGD:5509061 20180308 MGI PMID:29371219 1623721 Gemin4 gem nuclear organelle associated protein 4 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1623725 Kif26b kinesin family member 26B gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:20439720 1623725 Kif26b kinesin family member 26B gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20439720 1623725 Kif26b kinesin family member 26B gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:20439720 1623725 Kif26b kinesin family member 26B gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1623725 Kif26b kinesin family member 26B gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20439720 1623725 Kif26b kinesin family member 26B gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20160421 MGI 1623725 Kif26b kinesin family member 26B gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1623725 Kif26b kinesin family member 26B gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:20439720 1623725 Kif26b kinesin family member 26B gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20439720 1623725 Kif26b kinesin family member 26B gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:20439720 1623725 Kif26b kinesin family member 26B gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:20439720 1623725 Kif26b kinesin family member 26B gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:20439720 1623725 Kif26b kinesin family member 26B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623726 Nup54 nucleoporin 54 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 1623726 Nup54 nucleoporin 54 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20241010 MGI 1623726 Nup54 nucleoporin 54 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20241010 MGI 1623726 Nup54 nucleoporin 54 gene MP:0002582 disorganized extraembryonic tissue IEA N RGD:5509061 20241010 MGI 1623726 Nup54 nucleoporin 54 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20241010 MGI 1623726 Nup54 nucleoporin 54 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241010 MGI 1623726 Nup54 nucleoporin 54 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1623726 Nup54 nucleoporin 54 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1623749 Adam29 a disintegrin and metallopeptidase domain 29 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20240829 MGI PMID:38966569 1623749 Adam29 a disintegrin and metallopeptidase domain 29 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20240829 MGI PMID:38966569 1623749 Adam29 a disintegrin and metallopeptidase domain 29 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20240829 MGI PMID:38966569 1623749 Adam29 a disintegrin and metallopeptidase domain 29 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20240829 MGI PMID:38966569 1623749 Adam29 a disintegrin and metallopeptidase domain 29 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20240829 MGI PMID:38966569 1623749 Adam29 a disintegrin and metallopeptidase domain 29 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20240829 MGI PMID:38966569 1623749 Adam29 a disintegrin and metallopeptidase domain 29 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20240829 MGI PMID:38966569 1623749 Adam29 a disintegrin and metallopeptidase domain 29 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20240829 MGI PMID:38966569 1623749 Adam29 a disintegrin and metallopeptidase domain 29 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20240829 MGI PMID:38966569 1623749 Adam29 a disintegrin and metallopeptidase domain 29 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240829 MGI PMID:38966569 1623754 Hsd17b13 hydroxysteroid (17-beta) dehydrogenase 13 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20220407 MGI PMID:29401633 1623754 Hsd17b13 hydroxysteroid (17-beta) dehydrogenase 13 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170406 MGI 1623754 Hsd17b13 hydroxysteroid (17-beta) dehydrogenase 13 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20220407 MGI PMID:29401633 1623754 Hsd17b13 hydroxysteroid (17-beta) dehydrogenase 13 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20220407 MGI PMID:29401633 1623754 Hsd17b13 hydroxysteroid (17-beta) dehydrogenase 13 gene MP:0014174 decreased fatty acid beta-oxidation IAGP N RGD:5509061 20220407 MGI PMID:29401633 1623754 Hsd17b13 hydroxysteroid (17-beta) dehydrogenase 13 gene MP:0020867 increased lipogenesis IAGP N RGD:5509061 20220407 MGI PMID:29401633 1623754 Hsd17b13 hydroxysteroid (17-beta) dehydrogenase 13 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20220407 MGI PMID:29401633 1623754 Hsd17b13 hydroxysteroid (17-beta) dehydrogenase 13 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20220407 MGI PMID:29401633 1623757 Lsm14b LSM family member 14B gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20230914 MGI PMID:37083226 1623757 Lsm14b LSM family member 14B gene MP:0001926 female infertility IAGP N RGD:5509061 20230914 MGI PMID:37083226 1623757 Lsm14b LSM family member 14B gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20230914 MGI PMID:37083226 1623757 Lsm14b LSM family member 14B gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20230914 MGI PMID:37083226 1623757 Lsm14b LSM family member 14B gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1623757 Lsm14b LSM family member 14B gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20230914 MGI PMID:37083226 1623757 Lsm14b LSM family member 14B gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20230914 MGI PMID:37083226 1623757 Lsm14b LSM family member 14B gene MP:0009769 abnormal meiotic spindle assembly checkpoint IAGP N RGD:5509061 20230914 MGI PMID:37083226 1623757 Lsm14b LSM family member 14B gene MP:0013272 abnormal translation IAGP N RGD:5509061 20230914 MGI PMID:37083226 1623757 Lsm14b LSM family member 14B gene MP:0014443 impaired polar body extrusion IAGP N RGD:5509061 20240509 MGI PMID:37083226 1623757 Lsm14b LSM family member 14B gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20230914 MGI PMID:37083226 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:17210706 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:17210706 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:17210706 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17210706 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17210706 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:17210706 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:17959714 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:17210706 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:17210706 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0005167 abnormal blood-brain barrier function IAGP N RGD:5509061 20141003 MGI PMID:15314169 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0005167 abnormal blood-brain barrier function IAGP N RGD:5509061 20141003 MGI PMID:17210706 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0006088 abnormal blood-cerebrospinal fluid barrier function IAGP N RGD:5509061 20141003 MGI PMID:15314169 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0006272 abnormal urine organic anion level IAGP N RGD:5509061 20141003 MGI PMID:15314169 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17210706 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:17959714 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:17210706 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17210706 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17210706 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:17959714 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:17210706 1623761 Abcc4 ATP-binding cassette, sub-family C member 4 gene MP:0014348 decreased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:17210706 1623762 Otop2 otopetrin 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20201022 MGI PMID:29040572 1623762 Otop2 otopetrin 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20201022 MGI PMID:29040572 1623762 Otop2 otopetrin 2 gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20201022 MGI PMID:29040572 1623762 Otop2 otopetrin 2 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20201022 MGI PMID:29040572 1623762 Otop2 otopetrin 2 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20201022 MGI PMID:29040572 1623763 Sppl2c signal peptide peptidase 2C gene MP:0001925 male infertility IAGP N RGD:5509061 20221201 MGI PMID:35960805 1623763 Sppl2c signal peptide peptidase 2C gene MP:0001935 decreased litter size IAGP N RGD:5509061 20190926 MGI PMID:30733280 1623763 Sppl2c signal peptide peptidase 2C gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20190926 MGI PMID:30733280 1623763 Sppl2c signal peptide peptidase 2C gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20221201 MGI PMID:35960805 1623763 Sppl2c signal peptide peptidase 2C gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20190926 MGI PMID:30733280 1623763 Sppl2c signal peptide peptidase 2C gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210708 MGI PMID:32561905 1623763 Sppl2c signal peptide peptidase 2C gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20190926 MGI PMID:30733280 1623768 Rsad1 radical S-adenosyl methionine domain containing 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20160811 MGI 1623768 Rsad1 radical S-adenosyl methionine domain containing 1 gene MP:0000706 small thymus IEA N RGD:5509061 20160811 MGI 1623768 Rsad1 radical S-adenosyl methionine domain containing 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 1623768 Rsad1 radical S-adenosyl methionine domain containing 1 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20160811 MGI 1623768 Rsad1 radical S-adenosyl methionine domain containing 1 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20201022 MGI 1623768 Rsad1 radical S-adenosyl methionine domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20170105 MGI 1623772 Dmxl2 Dmx-like 2 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0001752 abnormal hypothalamus secretion IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0003550 short perineum IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 1623772 Dmxl2 Dmx-like 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200310 MGI 1623772 Dmxl2 Dmx-like 2 gene MP:0009008 delayed estrous cycle IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0009015 short proestrus IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 1623772 Dmxl2 Dmx-like 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1623772 Dmxl2 Dmx-like 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:25248098 1623772 Dmxl2 Dmx-like 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623772 Dmxl2 Dmx-like 2 gene MP:0011513 abnormal vertebral artery morphology IEA N RGD:5509061 20200310 MGI 1623772 Dmxl2 Dmx-like 2 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20200310 MGI 1623772 Dmxl2 Dmx-like 2 gene MP:0013968 multiple persisting craniopharyngeal ducts IEA N RGD:5509061 20200310 MGI 1623772 Dmxl2 Dmx-like 2 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20200310 MGI 1623772 Dmxl2 Dmx-like 2 gene MP:0014018 embryo tumor IEA N RGD:5509061 20200310 MGI 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0001147 small testis IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0001925 male infertility IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0011059 abnormal ependyma motile cilium morphology IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623773 Hoatz HOATZ cilia and flagella associated protein gene MP:0030964 decreased brain ependyma motile cilium length IAGP N RGD:5509061 20200528 MGI PMID:32248064 1623775 Tlcd5 TLC domain containing 5 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 1623775 Tlcd5 TLC domain containing 5 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20200402 MGI 1623777 Arhgef10 Rho guanine nucleotide exchange factor 10 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20190425 MGI PMID:29456827 1623777 Arhgef10 Rho guanine nucleotide exchange factor 10 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20190425 MGI PMID:29456827 1623777 Arhgef10 Rho guanine nucleotide exchange factor 10 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20190425 MGI PMID:29456827 1623777 Arhgef10 Rho guanine nucleotide exchange factor 10 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1623777 Arhgef10 Rho guanine nucleotide exchange factor 10 gene MP:0003063 increased coping response IAGP N RGD:5509061 20190425 MGI PMID:29456827 1623777 Arhgef10 Rho guanine nucleotide exchange factor 10 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20201022 MGI 1623777 Arhgef10 Rho guanine nucleotide exchange factor 10 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210520 MGI 1623777 Arhgef10 Rho guanine nucleotide exchange factor 10 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20190425 MGI PMID:29456827 1623777 Arhgef10 Rho guanine nucleotide exchange factor 10 gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20190425 MGI PMID:29456827 1623777 Arhgef10 Rho guanine nucleotide exchange factor 10 gene MP:0012636 decreased monoamine oxidase activity IAGP N RGD:5509061 20190425 MGI PMID:29456827 1623777 Arhgef10 Rho guanine nucleotide exchange factor 10 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20190425 MGI PMID:29456827 1623777 Arhgef10 Rho guanine nucleotide exchange factor 10 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:29456827 1623780 Prss58 serine protease 58 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210708 MGI PMID:32561905 1623781 Paqr3 progestin and adipoQ receptor family member III gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:18550569 1623781 Paqr3 progestin and adipoQ receptor family member III gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18550569 1623781 Paqr3 progestin and adipoQ receptor family member III gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:18550569 1623781 Paqr3 progestin and adipoQ receptor family member III gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:18550569 1623781 Paqr3 progestin and adipoQ receptor family member III gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:18550569 1623781 Paqr3 progestin and adipoQ receptor family member III gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18550569 1623782 Cox18 cytochrome c oxidase assembly protein 18 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20210128 MGI 1623782 Cox18 cytochrome c oxidase assembly protein 18 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20210128 MGI 1623782 Cox18 cytochrome c oxidase assembly protein 18 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1623782 Cox18 cytochrome c oxidase assembly protein 18 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220519 MGI 1623782 Cox18 cytochrome c oxidase assembly protein 18 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623782 Cox18 cytochrome c oxidase assembly protein 18 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210520 MGI 1623787 Phf20 PHD finger protein 20 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0000692 small spleen IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0000706 small thymus IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20160304 MGI PMID:22072714 1623787 Phf20 PHD finger protein 20 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1623788 Pigu phosphatidylinositol glycan anchor biosynthesis, class U gene MP:0001891 hydrocephaly IEA N RGD:5509061 20160811 MGI 1623788 Pigu phosphatidylinositol glycan anchor biosynthesis, class U gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623790 Bpifb1 BPI fold containing family B, member 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1623790 Bpifb1 BPI fold containing family B, member 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20171221 MGI PMID:28851744 1623790 Bpifb1 BPI fold containing family B, member 1 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20171221 MGI PMID:28851744 1623790 Bpifb1 BPI fold containing family B, member 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1623790 Bpifb1 BPI fold containing family B, member 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20170105 MGI 1623791 Proser2 proline and serine rich 2 gene MP:0000280 thin ventricular wall IEA N RGD:5509061 20230601 MGI 1623791 Proser2 proline and serine rich 2 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20230119 MGI 1623791 Proser2 proline and serine rich 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 1623791 Proser2 proline and serine rich 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 1623791 Proser2 proline and serine rich 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230119 MGI 1623791 Proser2 proline and serine rich 2 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 1623791 Proser2 proline and serine rich 2 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 1623791 Proser2 proline and serine rich 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230119 MGI 1623791 Proser2 proline and serine rich 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230119 MGI 1623791 Proser2 proline and serine rich 2 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 1623791 Proser2 proline and serine rich 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230119 MGI 1623791 Proser2 proline and serine rich 2 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20230119 MGI 1623791 Proser2 proline and serine rich 2 gene MP:0011625 cystolithiasis IEA N RGD:5509061 20230119 MGI 1623792 Cdnf cerebral dopamine neurotrophic factor gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20200402 MGI PMID:31783118 1623792 Cdnf cerebral dopamine neurotrophic factor gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 1623792 Cdnf cerebral dopamine neurotrophic factor gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20200402 MGI PMID:31783118 1623792 Cdnf cerebral dopamine neurotrophic factor gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200402 MGI PMID:31783118 1623792 Cdnf cerebral dopamine neurotrophic factor gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 1623792 Cdnf cerebral dopamine neurotrophic factor gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 1623792 Cdnf cerebral dopamine neurotrophic factor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200402 MGI PMID:31783118 1623792 Cdnf cerebral dopamine neurotrophic factor gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20200402 MGI PMID:31783118 1623792 Cdnf cerebral dopamine neurotrophic factor gene MP:0010800 abnormal submucous nerve plexus morphology IAGP N RGD:5509061 20200402 MGI PMID:31783118 1623792 Cdnf cerebral dopamine neurotrophic factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200402 MGI PMID:31783118 1623792 Cdnf cerebral dopamine neurotrophic factor gene MP:0012134 absent umbilical cord IAGP N RGD:5509061 20200402 MGI PMID:31783118 1623792 Cdnf cerebral dopamine neurotrophic factor gene MP:0012299 hydropic allantois IAGP N RGD:5509061 20200402 MGI PMID:31783118 1623792 Cdnf cerebral dopamine neurotrophic factor gene MP:0020876 increased nervous system dopamine level IAGP N RGD:5509061 20200402 MGI PMID:31783118 1623792 Cdnf cerebral dopamine neurotrophic factor gene MP:0030585 enhanced behavioral response to amphetamine IAGP N RGD:5509061 20200402 MGI PMID:31783118 1623792 Cdnf cerebral dopamine neurotrophic factor gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20200402 MGI PMID:31783118 1623793 Ablim1 actin-binding LIM protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12849746 1623795 Crb3 crumbs family member 3 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:24164893 1623795 Crb3 crumbs family member 3 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:24164893 1623795 Crb3 crumbs family member 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20160304 MGI PMID:26631503 1623795 Crb3 crumbs family member 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:24164893 1623795 Crb3 crumbs family member 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20160304 MGI PMID:26631503 1623795 Crb3 crumbs family member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160304 MGI PMID:26631503 1623795 Crb3 crumbs family member 3 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:24164893 1623795 Crb3 crumbs family member 3 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:24164893 1623795 Crb3 crumbs family member 3 gene MP:0002989 small kidney IAGP N RGD:5509061 20160304 MGI PMID:26631503 1623795 Crb3 crumbs family member 3 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20160304 MGI PMID:26631503 1623795 Crb3 crumbs family member 3 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:24164893 1623795 Crb3 crumbs family member 3 gene MP:0004391 abnormal respiratory conducting tube morphology IAGP N RGD:5509061 20160304 MGI PMID:26631503 1623795 Crb3 crumbs family member 3 gene MP:0004967 abnormal kidney epithelium morphology IAGP N RGD:5509061 20160304 MGI PMID:26631503 1623795 Crb3 crumbs family member 3 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20160304 MGI PMID:26631503 1623795 Crb3 crumbs family member 3 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:24164893 1623795 Crb3 crumbs family member 3 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20160304 MGI PMID:26631503 1623795 Crb3 crumbs family member 3 gene MP:0008109 abnormal small intestinal microvillus morphology IAGP N RGD:5509061 20141003 MGI PMID:24164893 1623795 Crb3 crumbs family member 3 gene MP:0008141 decreased small intestinal microvillus size IAGP N RGD:5509061 20141003 MGI PMID:24164893 1623795 Crb3 crumbs family member 3 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20160304 MGI PMID:26631503 1623795 Crb3 crumbs family member 3 gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20160310 MGI PMID:26631503 1623795 Crb3 crumbs family member 3 gene MP:0010809 abnormal club cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24164893 1623795 Crb3 crumbs family member 3 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:24164893 1623795 Crb3 crumbs family member 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24164893 1623795 Crb3 crumbs family member 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20160304 MGI PMID:26631503 1623795 Crb3 crumbs family member 3 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24164893 1623795 Crb3 crumbs family member 3 gene MP:0011350 abnormal proximal convoluted tubule brush border morphology IAGP N RGD:5509061 20141003 MGI PMID:24164893 1623795 Crb3 crumbs family member 3 gene MP:0014080 fused small intestinal villi IAGP N RGD:5509061 20160310 MGI PMID:24164893 1623795 Crb3 crumbs family member 3 gene MP:0014080 fused small intestinal villi IAGP N RGD:5509061 20160310 MGI PMID:26631503 1623795 Crb3 crumbs family member 3 gene MP:0014473 increased pulmonary alveolus wall thickness IAGP N RGD:5509061 20240704 MGI PMID:24164893 1623798 Micos13 mitochondrial contact site and cristae organizing system subunit 13 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 1623798 Micos13 mitochondrial contact site and cristae organizing system subunit 13 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20231207 MGI 1623798 Micos13 mitochondrial contact site and cristae organizing system subunit 13 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 1623798 Micos13 mitochondrial contact site and cristae organizing system subunit 13 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20231207 MGI 1623798 Micos13 mitochondrial contact site and cristae organizing system subunit 13 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 1623799 Safb scaffold attachment factor B gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0003700 abnormal oviduct transport IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0005647 abnormal sex gland physiology IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0009064 oviduct atrophy IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0009070 small oviduct IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0010995 abnormal lung alveolus development IAGP N RGD:5509061 20141204 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0013318 abnormal branching involved in seminal vesicle morphogenesis IAGP N RGD:5509061 20141204 MGI PMID:15798188 1623799 Safb scaffold attachment factor B gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:15798188 1623800 Safb2 scaffold attachment factor B2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 1623800 Safb2 scaffold attachment factor B2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 1623800 Safb2 scaffold attachment factor B2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1623800 Safb2 scaffold attachment factor B2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1623800 Safb2 scaffold attachment factor B2 gene MP:0002776 increased Sertoli cell number IAGP N RGD:5509061 20151119 MGI PMID:26092125 1623800 Safb2 scaffold attachment factor B2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210128 MGI 1623800 Safb2 scaffold attachment factor B2 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20151119 MGI PMID:26092125 1623800 Safb2 scaffold attachment factor B2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 1623800 Safb2 scaffold attachment factor B2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 1623800 Safb2 scaffold attachment factor B2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1623801 Tomm22 translocase of outer mitochondrial membrane 22 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 1623801 Tomm22 translocase of outer mitochondrial membrane 22 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623801 Tomm22 translocase of outer mitochondrial membrane 22 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1623804 Eppk1 epiplakin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16382147 1623804 Eppk1 epiplakin 1 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:16382146 1623804 Eppk1 epiplakin 1 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18285451 1623804 Eppk1 epiplakin 1 gene MP:0012193 increased keratinocyte migration IAGP N RGD:5509061 20141204 MGI PMID:16382146 1623809 Kcnk9 potassium channel, subfamily K, member 9 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:18250325 1623809 Kcnk9 potassium channel, subfamily K, member 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17728447 1623809 Kcnk9 potassium channel, subfamily K, member 9 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:18250325 1623809 Kcnk9 potassium channel, subfamily K, member 9 gene MP:0002909 abnormal adrenal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:18250325 1623809 Kcnk9 potassium channel, subfamily K, member 9 gene MP:0003353 decreased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:18250325 1623809 Kcnk9 potassium channel, subfamily K, member 9 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:18250325 1623809 Kcnk9 potassium channel, subfamily K, member 9 gene MP:0004119 hypokalemia IAGP N RGD:5509061 20141003 MGI PMID:18250325 1623809 Kcnk9 potassium channel, subfamily K, member 9 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:18250325 1623809 Kcnk9 potassium channel, subfamily K, member 9 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:18094244 1623810 Wdr41 WD repeat domain 41 gene MP:0001399 hyperactivity IEA N RGD:5509061 20190502 MGI 1623810 Wdr41 WD repeat domain 41 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 1623810 Wdr41 WD repeat domain 41 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1623810 Wdr41 WD repeat domain 41 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1623810 Wdr41 WD repeat domain 41 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190124 MGI PMID:30442666 1623810 Wdr41 WD repeat domain 41 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20190124 MGI PMID:30442666 1623810 Wdr41 WD repeat domain 41 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20190124 MGI PMID:30442666 1623810 Wdr41 WD repeat domain 41 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20190124 MGI PMID:30442666 1623810 Wdr41 WD repeat domain 41 gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20190124 MGI PMID:30442666 1623810 Wdr41 WD repeat domain 41 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 1623813 Gpr179 G protein-coupled receptor 179 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22325362 1623813 Gpr179 G protein-coupled receptor 179 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22896717 1623813 Gpr179 G protein-coupled receptor 179 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22325362 1623814 Prr15l proline rich 15-like gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20230601 MGI 1623814 Prr15l proline rich 15-like gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1623814 Prr15l proline rich 15-like gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1623815 Spata20 spermatogenesis associated 20 gene MP:0001147 small testis IAGP N RGD:5509061 20180712 MGI PMID:29247744 1623815 Spata20 spermatogenesis associated 20 gene MP:0001925 male infertility IAGP N RGD:5509061 20180712 MGI PMID:29247744 1623815 Spata20 spermatogenesis associated 20 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20180712 MGI PMID:29247744 1623815 Spata20 spermatogenesis associated 20 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20180712 MGI PMID:29247744 1623815 Spata20 spermatogenesis associated 20 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20180712 MGI PMID:29247744 1623815 Spata20 spermatogenesis associated 20 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180712 MGI PMID:29247744 1623815 Spata20 spermatogenesis associated 20 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20180712 MGI PMID:29247744 1623815 Spata20 spermatogenesis associated 20 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20180712 MGI PMID:29247744 1623815 Spata20 spermatogenesis associated 20 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20180712 MGI PMID:29247744 1623815 Spata20 spermatogenesis associated 20 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20180712 MGI PMID:29247744 1623815 Spata20 spermatogenesis associated 20 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20180712 MGI PMID:29247744 1623815 Spata20 spermatogenesis associated 20 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20180712 MGI PMID:29247744 1623815 Spata20 spermatogenesis associated 20 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20180712 MGI PMID:29247744 1623815 Spata20 spermatogenesis associated 20 gene MP:0031373 abnormal manchette perinuclear ring morphology IAGP N RGD:5509061 20220407 MGI PMID:29247744 1623818 Nhsl1 NHS like 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200310 MGI 1623818 Nhsl1 NHS like 1 gene MP:0001147 small testis IEA N RGD:5509061 20200310 MGI 1623818 Nhsl1 NHS like 1 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20200310 MGI 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20210128 MGI 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210128 MGI 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200310 MGI PMID:27233614 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:27233614 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:23776622 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200310 MGI PMID:23776622 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:27233614 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20200310 MGI PMID:27233614 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200310 MGI PMID:27233614 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:23776622 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200310 MGI PMID:27233614 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:23776622 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:27233614 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200310 MGI PMID:27233614 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20210128 MGI 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:23776622 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20200310 MGI PMID:23776622 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20210128 MGI 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20200310 MGI PMID:23776622 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:23776622 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200310 MGI PMID:27233614 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20210128 MGI 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:23776622 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20210128 MGI 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:27233614 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20200310 MGI PMID:27233614 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:27233614 1623819 Sidt2 SID1 transmembrane family, member 2 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20200310 MGI PMID:27233614 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0000243 myoclonus IAGP N RGD:5509061 20200310 MGI PMID:11544478 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:11544478 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0001393 ataxia IAGP N RGD:5509061 20200310 MGI PMID:11544478 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0002183 gliosis IAGP N RGD:5509061 20200310 MGI PMID:11544478 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20200310 MGI PMID:11544478 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0003216 absence seizures IAGP N RGD:5509061 20200310 MGI PMID:15262267 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20200310 MGI PMID:15262267 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20200310 MGI PMID:15262267 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:11544478 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0030707 decreased glutamine level IAGP N RGD:5509061 20200310 MGI PMID:12067239 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0030707 decreased glutamine level IAGP N RGD:5509061 20200310 MGI PMID:15262267 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0030730 increased beta-alanine level IAGP N RGD:5509061 20200310 MGI PMID:12067239 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0030732 increased gamma-aminobutyric acid level IAGP N RGD:5509061 20200310 MGI PMID:11544478 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0030732 increased gamma-aminobutyric acid level IAGP N RGD:5509061 20200310 MGI PMID:12067239 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0030732 increased gamma-aminobutyric acid level IAGP N RGD:5509061 20200310 MGI PMID:15262267 1623821 Aldh5a1 aldhehyde dehydrogenase family 5, subfamily A1 gene MP:0030734 increased urine gamma-aminobutyric acid level IAGP N RGD:5509061 20200310 MGI PMID:11544478 1623822 Tdrd5 tudor domain containing 5 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21383078 1623822 Tdrd5 tudor domain containing 5 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:21383078 1623822 Tdrd5 tudor domain containing 5 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21383078 1623822 Tdrd5 tudor domain containing 5 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20180531 MGI PMID:29317670 1623822 Tdrd5 tudor domain containing 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21383078 1623822 Tdrd5 tudor domain containing 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20180531 MGI PMID:29317670 1623822 Tdrd5 tudor domain containing 5 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21383078 1623822 Tdrd5 tudor domain containing 5 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20180531 MGI PMID:29317670 1623822 Tdrd5 tudor domain containing 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21383078 1623822 Tdrd5 tudor domain containing 5 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180531 MGI PMID:29317670 1623822 Tdrd5 tudor domain containing 5 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21383078 1623822 Tdrd5 tudor domain containing 5 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21383078 1623822 Tdrd5 tudor domain containing 5 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21383078 1623822 Tdrd5 tudor domain containing 5 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21383078 1623822 Tdrd5 tudor domain containing 5 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:21383078 1623824 Cep164 centrosomal protein 164 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0000440 domed cranium IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0001925 male infertility IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0001925 male infertility IAGP N RGD:5509061 20211209 MGI PMID:34085951 1623824 Cep164 centrosomal protein 164 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20211209 MGI PMID:34085951 1623824 Cep164 centrosomal protein 164 gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20211209 MGI PMID:34085951 1623824 Cep164 centrosomal protein 164 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20211209 MGI PMID:34085951 1623824 Cep164 centrosomal protein 164 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20211209 MGI PMID:34085951 1623824 Cep164 centrosomal protein 164 gene MP:0004728 abnormal efferent ductules of testis morphology IAGP N RGD:5509061 20211209 MGI PMID:34085951 1623824 Cep164 centrosomal protein 164 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0005159 azoospermia IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20211209 MGI PMID:34085951 1623824 Cep164 centrosomal protein 164 gene MP:0006308 enlarged seminiferous tubules IAGP N RGD:5509061 20211209 MGI PMID:34085951 1623824 Cep164 centrosomal protein 164 gene MP:0006417 rete testis obstruction IAGP N RGD:5509061 20211209 MGI PMID:34085951 1623824 Cep164 centrosomal protein 164 gene MP:0006423 dilated rete testis IAGP N RGD:5509061 20211209 MGI PMID:34085951 1623824 Cep164 centrosomal protein 164 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20211209 MGI PMID:34085951 1623824 Cep164 centrosomal protein 164 gene MP:0009140 dilated efferent ductule of testis IAGP N RGD:5509061 20211209 MGI PMID:34085951 1623824 Cep164 centrosomal protein 164 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20211209 MGI PMID:34085951 1623824 Cep164 centrosomal protein 164 gene MP:0009257 dilated seminiferous tubule IAGP N RGD:5509061 20211209 MGI PMID:34085951 1623824 Cep164 centrosomal protein 164 gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0011053 decreased respiratory motile cilia number IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623824 Cep164 centrosomal protein 164 gene MP:0011281 abnormal olfactory epithelium cilium morphology IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0011644 abnormal oviduct epithelium motile cilium morphology IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20211209 MGI PMID:34085951 1623824 Cep164 centrosomal protein 164 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0013214 decreased embryonic neuroepithelium primary cilium number IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0030963 abnormal brain ependyma motile cilium location or orientation IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0030966 decreased brain ependyma motile cilium number IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0031088 coughing IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623824 Cep164 centrosomal protein 164 gene MP:0031089 sneezing IAGP N RGD:5509061 20210729 MGI PMID:29244804 1623826 Tmprss13 transmembrane protease, serine 13 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20200310 MGI PMID:24832573 1623826 Tmprss13 transmembrane protease, serine 13 gene MP:0001282 short vibrissae IAGP N RGD:5509061 20200310 MGI PMID:24832573 1623826 Tmprss13 transmembrane protease, serine 13 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20200310 MGI 1623826 Tmprss13 transmembrane protease, serine 13 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20200310 MGI PMID:24832573 1623827 Wdr49 WD repeat domain 49 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1623827 Wdr49 WD repeat domain 49 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1623827 Wdr49 WD repeat domain 49 gene MP:0002981 increased liver weight IEA N RGD:5509061 20221215 MGI 1623828 Il20rb interleukin 20 receptor beta gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1623828 Il20rb interleukin 20 receptor beta gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 1623828 Il20rb interleukin 20 receptor beta gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 1623828 Il20rb interleukin 20 receptor beta gene MP:0001891 hydrocephaly IEA N RGD:5509061 20170105 MGI 1623828 Il20rb interleukin 20 receptor beta gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 1623828 Il20rb interleukin 20 receptor beta gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210128 MGI 1623828 Il20rb interleukin 20 receptor beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18264109 1623828 Il20rb interleukin 20 receptor beta gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20181227 MGI 1623828 Il20rb interleukin 20 receptor beta gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20210520 MGI 1623828 Il20rb interleukin 20 receptor beta gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17074928 1623828 Il20rb interleukin 20 receptor beta gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20170105 MGI 1623828 Il20rb interleukin 20 receptor beta gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19124723 1623828 Il20rb interleukin 20 receptor beta gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19124723 1623828 Il20rb interleukin 20 receptor beta gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:19124723 1623828 Il20rb interleukin 20 receptor beta gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:19124723 1623828 Il20rb interleukin 20 receptor beta gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19124723 1623828 Il20rb interleukin 20 receptor beta gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19124723 1623828 Il20rb interleukin 20 receptor beta gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:19124723 1623828 Il20rb interleukin 20 receptor beta gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19124723 1623828 Il20rb interleukin 20 receptor beta gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19124723 1623828 Il20rb interleukin 20 receptor beta gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220811 MGI 1623828 Il20rb interleukin 20 receptor beta gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1623829 Tmem18 transmembrane protein 18 gene MP:0001260 increased body weight IAGP N RGD:5509061 20180308 MGI PMID:28811369 1623829 Tmem18 transmembrane protein 18 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20180308 MGI PMID:28811369 1623829 Tmem18 transmembrane protein 18 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20180308 MGI PMID:28811369 1623829 Tmem18 transmembrane protein 18 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20181227 MGI 1623829 Tmem18 transmembrane protein 18 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180308 MGI PMID:28811369 1623829 Tmem18 transmembrane protein 18 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20180308 MGI PMID:28811369 1623829 Tmem18 transmembrane protein 18 gene MP:0011939 increased food intake IAGP N RGD:5509061 20180308 MGI PMID:28811369 1623829 Tmem18 transmembrane protein 18 gene MP:0013630 increased bone trabecular spacing IEA N RGD:5509061 20211021 MGI 1623829 Tmem18 transmembrane protein 18 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20180308 MGI PMID:28811369 1623829 Tmem18 transmembrane protein 18 gene MP:0014170 increased brown adipose tissue mass IAGP N RGD:5509061 20180308 MGI PMID:28811369 1623831 Asap2 ArfGAP with SH3 domain, ankyrin repeat and PH domain 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 1623837 Cstdc3 cystatin domain containing 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1623837 Cstdc3 cystatin domain containing 3 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20210128 MGI 1623837 Cstdc3 cystatin domain containing 3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20210128 MGI 1623838 Chmp6 charged multivesicular body protein 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623838 Chmp6 charged multivesicular body protein 6 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1623838 Chmp6 charged multivesicular body protein 6 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1623840 Pknox2 Pbx/knotted 1 homeobox 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200514 MGI 1623840 Pknox2 Pbx/knotted 1 homeobox 2 gene MP:0000692 small spleen IEA N RGD:5509061 20200514 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0000189 hypoglycemia IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0001262 decreased body weight IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0002497 increased IgE level IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0004978 decreased B-1 B cell number IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0005017 decreased B cell number IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0005018 decreased T cell number IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0008083 decreased single-positive T cell number IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0008126 increased dendritic cell number IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0008170 decreased B-1b cell number IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0008560 increased tumor necrosis factor secretion IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0008658 decreased interleukin-1 beta secretion IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0009787 increased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0010848 decreased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0011078 increased macrophage cytokine production IAGP N RGD:5509061 20141003 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0011080 increased macrophage apoptosis IEA N RGD:5509061 20181011 MGI 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:23219391 1623841 Nlrp1a NLR family, pyrin domain containing 1A gene MP:0031110 meningitis IAGP N RGD:5509061 20200910 MGI PMID:23219391 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170126 MGI PMID:25580854 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0001265 decreased body size IAGP N RGD:5509061 20170126 MGI PMID:25580854 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20170126 MGI PMID:25580854 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20170126 MGI PMID:25580854 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20170126 MGI PMID:25580854 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20170126 MGI PMID:25580854 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20170126 MGI PMID:25580854 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20170126 MGI PMID:25580854 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0010093 decreased circulating magnesium level IEA N RGD:5509061 20201022 MGI 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20170126 MGI PMID:25580854 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170126 MGI PMID:25580854 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1623843 Abhd16a abhydrolase domain containing 16A gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210520 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20201022 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0000226 abnormal mean corpuscular volume IEA N RGD:5509061 20201231 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200514 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0001147 small testis IEA N RGD:5509061 20200514 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20200514 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20200514 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0004930 small epididymis IEA N RGD:5509061 20200514 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20200514 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0005265 abnormal blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20200514 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0008428 abnormal spatial working memory IEA N RGD:5509061 20231207 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 1623844 Ube2j2 ubiquitin-conjugating enzyme E2J 2 gene MP:0011898 abnormal platelet cell number IEA N RGD:5509061 20210826 MGI 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:24192035 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0000445 short snout IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0000478 delayed intestine development IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:24192035 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20200310 MGI PMID:24192035 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20200310 MGI PMID:24192035 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:24192035 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20111116 MGI 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0001394 circling IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20111116 MGI 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:23764754 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20200310 MGI PMID:24192035 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20200310 MGI PMID:24192035 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:22948660 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0005655 increased aggression IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0008109 abnormal small intestinal microvillus morphology IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0008802 abnormal intestinal smooth muscle morphology IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0008987 abnormal liver lobule morphology IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20200310 MGI PMID:24192035 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0012207 decreased neuronal stem cell self-renewal IAGP N RGD:5509061 20200310 MGI PMID:24192035 1623845 Igf2bp1 insulin-like growth factor 2 mRNA binding protein 1 gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20200310 MGI PMID:15121863 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:19161597 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18547789 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12697902 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16227600 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18547789 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:18547789 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:12697902 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:18547789 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:19161597 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:19161597 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:16581056 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19161597 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19502490 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18547789 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:12697902 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:16227600 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:18547789 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:19161597 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:12697902 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:16227600 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16227600 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:12697902 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:19502490 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22037762 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19502490 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18547789 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12697902 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16227600 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:12697902 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:16227600 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:16581056 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12697902 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16885355 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18547789 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:12697902 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0004606 absent vertebral spinous process IAGP N RGD:5509061 20141003 MGI PMID:19161597 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:19161597 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:19161597 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:12697902 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:19161597 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:19161597 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:18547789 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:16581056 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:18547789 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0008832 hemivertebra IAGP N RGD:5509061 20141003 MGI PMID:19161597 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19502490 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18547789 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0010897 abnormal bronchiole epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19502490 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0010915 increased solitary pulmonary neuroendocrine cell number IAGP N RGD:5509061 20141003 MGI PMID:19502490 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0010942 abnormal respiratory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19502490 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0011071 absent club cells IAGP N RGD:5509061 20141003 MGI PMID:19502490 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19502490 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16885355 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18547789 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:12697902 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:16227600 1623846 Pofut1 protein O-fucosyltransferase 1 gene MP:0012254 absent intersomitic vessels IAGP N RGD:5509061 20141003 MGI PMID:12697902 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:17873059 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:17873059 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20200310 MGI PMID:17873059 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:17873059 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:17873059 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200310 MGI PMID:17873059 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:15314164 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:15314164 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:15314164 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200310 MGI PMID:16845469 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20200310 MGI PMID:17873059 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:17873059 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20200310 MGI PMID:17873059 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20200310 MGI PMID:15314164 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:17873059 1623847 Dmbx1 diencephalon/mesencephalon homeobox 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20200310 MGI PMID:17873059 1623848 Strc stereocilin gene MP:0004412 abnormal cochlear microphonics IAGP N RGD:5509061 20141003 MGI PMID:18849963 1623848 Strc stereocilin gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:18849963 1623848 Strc stereocilin gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:18849963 1623848 Strc stereocilin gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:18849963 1623848 Strc stereocilin gene MP:0006335 abnormal hearing electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18849963 1623848 Strc stereocilin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1623848 Strc stereocilin gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 1623849 Cts3 cathepsin 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20240523 MGI 1623850 Or5d18 olfactory receptor family 5 subfamily D member 18 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:21613506 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20150319 MGI PMID:25001218 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20201022 MGI 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150319 MGI PMID:25001218 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150319 MGI PMID:25001218 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20150319 MGI PMID:25001218 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20201022 MGI 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150319 MGI PMID:25001218 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20150319 MGI PMID:25001218 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20150319 MGI PMID:25001218 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20150319 MGI PMID:25001218 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0002764 short tibia IEA N RGD:5509061 20160421 MGI 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20150319 MGI PMID:25001218 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0003769 abnormal lip morphology IEA N RGD:5509061 20160421 MGI 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20150319 MGI PMID:25001218 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20150319 MGI PMID:25001218 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20150319 MGI PMID:25001218 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23077600 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20150319 MGI PMID:25001218 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623858 Mbd5 methyl-CpG binding domain protein 5 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 1623860 Sobp sine oculis binding protein gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:16962269 1623860 Sobp sine oculis binding protein gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:16235133 1623860 Sobp sine oculis binding protein gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:16962269 1623860 Sobp sine oculis binding protein gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:16962269 1623860 Sobp sine oculis binding protein gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16962269 1623860 Sobp sine oculis binding protein gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20111116 MGI 1623860 Sobp sine oculis binding protein gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:16962269 1623860 Sobp sine oculis binding protein gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 1623860 Sobp sine oculis binding protein gene MP:0008307 short scala media IAGP N RGD:5509061 20141003 MGI PMID:16962269 1623860 Sobp sine oculis binding protein gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16962269 1623860 Sobp sine oculis binding protein gene MP:0011968 decreased threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16962269 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220519 MGI 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0000613 abnormal salivary gland morphology IEA N RGD:5509061 20220519 MGI 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0000692 small spleen IEA N RGD:5509061 20220519 MGI 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220519 MGI 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20231130 MGI PMID:32616804 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20200514 MGI 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20231130 MGI PMID:32616804 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0002637 small uterus IEA N RGD:5509061 20220519 MGI 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20231130 MGI PMID:32616804 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20231130 MGI PMID:32616804 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210520 MGI 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20231130 MGI PMID:32616804 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20231130 MGI PMID:32616804 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0009516 enlarged salivary gland IEA N RGD:5509061 20220519 MGI 1623865 Phrf1 PHD and ring finger domains 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20231130 MGI PMID:32616804 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20200310 MGI PMID:16356929 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20200310 MGI PMID:21106871 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:21106871 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20200310 MGI PMID:16356929 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20200310 MGI PMID:21106871 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20200827 MGI PMID:31696216 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200827 MGI PMID:31696216 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200827 MGI PMID:31696216 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200310 MGI PMID:21106871 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20200310 MGI PMID:18779947 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20200310 MGI PMID:21106871 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20200827 MGI PMID:31696216 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200827 MGI PMID:31696216 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:21106871 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200310 MGI PMID:16356929 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200310 MGI PMID:18779947 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20200827 MGI PMID:31696216 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20200827 MGI PMID:31696216 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20200827 MGI PMID:31696216 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20200827 MGI PMID:31696216 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20200827 MGI PMID:31696216 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20200310 MGI PMID:21106871 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20200310 MGI PMID:21106871 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0009428 decreased tibialis anterior weight IAGP N RGD:5509061 20200310 MGI PMID:21106871 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20200310 MGI PMID:21106871 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20200310 MGI PMID:21106871 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20200827 MGI PMID:31696216 1623867 H6pd hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) gene MP:0020868 decreased lipogenesis IAGP N RGD:5509061 20200827 MGI PMID:31696216 1623868 Akna AT-hook transcription factor gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20160915 MGI PMID:21606955 1623868 Akna AT-hook transcription factor gene MP:0000746 weakness IAGP N RGD:5509061 20160915 MGI PMID:21606955 1623868 Akna AT-hook transcription factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20160915 MGI PMID:21606955 1623868 Akna AT-hook transcription factor gene MP:0001861 lung inflammation IAGP N RGD:5509061 20160915 MGI PMID:21606955 1623868 Akna AT-hook transcription factor gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20160915 MGI PMID:21606955 1623868 Akna AT-hook transcription factor gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20160915 MGI PMID:21606955 1623868 Akna AT-hook transcription factor gene MP:0010922 alveolitis IAGP N RGD:5509061 20160915 MGI PMID:21606955 1623868 Akna AT-hook transcription factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160915 MGI PMID:21606955 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17609112 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9636176 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17609112 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:17609112 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17609112 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17609112 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17609112 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:17609112 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:17609112 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0004156 abnormal QT variability IEA N RGD:5509061 20220519 MGI 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17609112 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:17609112 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17609112 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17609112 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17609112 1623869 Phactr4 phosphatase and actin regulator 4 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17609112 1623871 Shoc1 shortage in chiasmata 1 gene MP:0001147 small testis IAGP N RGD:5509061 20180628 MGI PMID:29742103 1623871 Shoc1 shortage in chiasmata 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20180628 MGI PMID:29742103 1623871 Shoc1 shortage in chiasmata 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180628 MGI PMID:29742103 1623871 Shoc1 shortage in chiasmata 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20180628 MGI PMID:29742103 1623871 Shoc1 shortage in chiasmata 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20180628 MGI PMID:29742103 1623871 Shoc1 shortage in chiasmata 1 gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20180628 MGI PMID:29742103 1623871 Shoc1 shortage in chiasmata 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20180628 MGI PMID:29742103 1623871 Shoc1 shortage in chiasmata 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180628 MGI PMID:29742103 1623871 Shoc1 shortage in chiasmata 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20180628 MGI PMID:29742103 1623872 Pcdhgb1 protocadherin gamma subfamily B, 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201022 MGI 1623874 Chrac1 chromatin accessibility complex 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20231207 MGI 1623874 Chrac1 chromatin accessibility complex 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20231207 MGI 1623875 Selenof selenoprotein F gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:21768092 1623875 Selenof selenoprotein F gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:21768092 1623875 Selenof selenoprotein F gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21768092 1623875 Selenof selenoprotein F gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:21768092 1623875 Selenof selenoprotein F gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:21768092 1623875 Selenof selenoprotein F gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:21768092 1623877 Nat8f2 N-acetyltransferase 8 (GCN5-related) family member 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 1623877 Nat8f2 N-acetyltransferase 8 (GCN5-related) family member 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210826 MGI 1623878 Rnf123 ring finger protein 123 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240523 MGI 1623878 Rnf123 ring finger protein 123 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20240425 MGI PMID:35063657 1623878 Rnf123 ring finger protein 123 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20240425 MGI PMID:35063657 1623878 Rnf123 ring finger protein 123 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20240523 MGI 1623878 Rnf123 ring finger protein 123 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 1623878 Rnf123 ring finger protein 123 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20240523 MGI 1623878 Rnf123 ring finger protein 123 gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20240425 MGI PMID:35063657 1623878 Rnf123 ring finger protein 123 gene MP:0010751 decreased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20240425 MGI PMID:35063657 1623878 Rnf123 ring finger protein 123 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1623880 Zfpl1 zinc finger like protein 1 gene MP:0000745 tremors IEA N RGD:5509061 20190502 MGI 1623880 Zfpl1 zinc finger like protein 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20220811 MGI 1623883 Crisp4 cysteine-rich secretory protein 4 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:21482758 1623883 Crisp4 cysteine-rich secretory protein 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21865554 1623887 Tmem190 transmembrane protein 190 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21273369 1623890 Tmem234 transmembrane protein 234 gene MP:0008500 increased IgG2a level IEA N RGD:5509061 20170323 MGI 1623892 Spring1 SREBF pathway regulator in golgi 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200723 MGI PMID:32111832 1623892 Spring1 SREBF pathway regulator in golgi 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200723 MGI PMID:32111832 1623892 Spring1 SREBF pathway regulator in golgi 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20200723 MGI PMID:32111832 1623892 Spring1 SREBF pathway regulator in golgi 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200723 MGI PMID:32111832 1623892 Spring1 SREBF pathway regulator in golgi 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1623892 Spring1 SREBF pathway regulator in golgi 1 gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20200723 MGI PMID:32111832 1623894 Ppfia3 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 3 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20200402 MGI 1623894 Ppfia3 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220428 MGI 1623894 Ppfia3 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 3 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20220519 MGI 1623894 Ppfia3 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 3 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 1623894 Ppfia3 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20201210 MGI PMID:29439199 1623894 Ppfia3 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 3 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20200402 MGI 1623894 Ppfia3 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 3 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20201210 MGI PMID:29439199 1623894 Ppfia3 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 3 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20201210 MGI PMID:29439199 1623894 Ppfia3 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 3 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20201210 MGI PMID:29439199 1623894 Ppfia3 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 3 gene MP:0030950 abnormal synaptic vesicle exocytosis IAGP N RGD:5509061 20201210 MGI PMID:29439199 1623894 Ppfia3 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:29439199 1623895 Mettl4 methyltransferase 4, N6-adenosine gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20190919 MGI PMID:30982744 1623895 Mettl4 methyltransferase 4, N6-adenosine gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20190919 MGI PMID:30982744 1623895 Mettl4 methyltransferase 4, N6-adenosine gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20190919 MGI PMID:30982744 1623895 Mettl4 methyltransferase 4, N6-adenosine gene MP:0001293 anophthalmia IAGP N RGD:5509061 20190919 MGI PMID:30982744 1623895 Mettl4 methyltransferase 4, N6-adenosine gene MP:0001577 anemia IAGP N RGD:5509061 20190919 MGI PMID:30982744 1623895 Mettl4 methyltransferase 4, N6-adenosine gene MP:0001921 reduced fertility IAGP N RGD:5509061 20190919 MGI PMID:30982744 1623895 Mettl4 methyltransferase 4, N6-adenosine gene MP:0013139 moribund IAGP N RGD:5509061 20190919 MGI PMID:30982744 1623896 Cluap1 clusterin associated protein 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:23351563 1623896 Cluap1 clusterin associated protein 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:23742838 1623896 Cluap1 clusterin associated protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23351563 1623896 Cluap1 clusterin associated protein 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:23351563 1623896 Cluap1 clusterin associated protein 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:23351563 1623896 Cluap1 clusterin associated protein 1 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:23351563 1623896 Cluap1 clusterin associated protein 1 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:23742838 1623896 Cluap1 clusterin associated protein 1 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:23742838 1623896 Cluap1 clusterin associated protein 1 gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:23742838 1623896 Cluap1 clusterin associated protein 1 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:23742838 1623896 Cluap1 clusterin associated protein 1 gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:23742838 1623896 Cluap1 clusterin associated protein 1 gene MP:0011068 abnormal ependyma motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:23742838 1623896 Cluap1 clusterin associated protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23351563 1623896 Cluap1 clusterin associated protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23742838 1623896 Cluap1 clusterin associated protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23742838 1623896 Cluap1 clusterin associated protein 1 gene MP:0011998 decreased embryonic cilium length IAGP N RGD:5509061 20141003 MGI PMID:23742838 1623896 Cluap1 clusterin associated protein 1 gene MP:0012270 cardiac edema IAGP N RGD:5509061 20141003 MGI PMID:23742838 1623896 Cluap1 clusterin associated protein 1 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:23742838 1623904 1700003F12Rik RIKEN cDNA 1700003F12 gene gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201231 MGI 1623904 1700003F12Rik RIKEN cDNA 1700003F12 gene gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 1623904 1700003F12Rik RIKEN cDNA 1700003F12 gene gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 1623904 1700003F12Rik RIKEN cDNA 1700003F12 gene gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20160421 MGI 1623905 Cfap126 cilia and flagella associated protein 126 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22153975 1623906 Stpg4 sperm tail PG rich repeat containing 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1623906 Stpg4 sperm tail PG rich repeat containing 4 gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20210520 MGI 1623906 Stpg4 sperm tail PG rich repeat containing 4 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20230316 MGI PMID:28930672 1623908 Syce3 synaptonemal complex central element protein 3 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:21637789 1623908 Syce3 synaptonemal complex central element protein 3 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:21637789 1623908 Syce3 synaptonemal complex central element protein 3 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:21637789 1623908 Syce3 synaptonemal complex central element protein 3 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21637789 1623908 Syce3 synaptonemal complex central element protein 3 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21637789 1623908 Syce3 synaptonemal complex central element protein 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21637789 1623908 Syce3 synaptonemal complex central element protein 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21637789 1623908 Syce3 synaptonemal complex central element protein 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:21637789 1623908 Syce3 synaptonemal complex central element protein 3 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:21637789 1623908 Syce3 synaptonemal complex central element protein 3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:21637789 1623908 Syce3 synaptonemal complex central element protein 3 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:21637789 1623908 Syce3 synaptonemal complex central element protein 3 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21637789 1623908 Syce3 synaptonemal complex central element protein 3 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20141003 MGI PMID:21637789 1623908 Syce3 synaptonemal complex central element protein 3 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:21637789 1623910 Ascc2 activating signal cointegrator 1 complex subunit 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20161201 MGI 1623910 Ascc2 activating signal cointegrator 1 complex subunit 2 gene MP:0001512 trunk curl IEA N RGD:5509061 20201231 MGI 1623910 Ascc2 activating signal cointegrator 1 complex subunit 2 gene MP:0010580 decreased heart left ventricle size IEA N RGD:5509061 20190502 MGI 1623910 Ascc2 activating signal cointegrator 1 complex subunit 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623910 Ascc2 activating signal cointegrator 1 complex subunit 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1623916 Cfap97d1 CFAP97 domain containing 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20201112 MGI PMID:32785227 1623916 Cfap97d1 CFAP97 domain containing 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20201112 MGI PMID:32785227 1623916 Cfap97d1 CFAP97 domain containing 1 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201112 MGI PMID:32785227 1623916 Cfap97d1 CFAP97 domain containing 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1623916 Cfap97d1 CFAP97 domain containing 1 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20201112 MGI PMID:32785227 1623916 Cfap97d1 CFAP97 domain containing 1 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20201112 MGI PMID:32785227 1623917 Cimip2c ciliary microtubule inner protein 2C gene MP:0003960 increased lean body mass IEA N RGD:5509061 20231207 MGI 1623919 Cfap144 cilia and flagella associated protein 144 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:30279523 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0000914 exencephaly IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0000929 open neural tube IAGP N RGD:5509061 20200310 MGI PMID:16540515 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20200310 MGI PMID:16540515 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200310 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20200310 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20200310 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0001785 edema IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200310 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0001926 female infertility IAGP N RGD:5509061 20200310 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:16540515 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0002678 increased follicle recruitment IAGP N RGD:5509061 20200310 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20200310 MGI PMID:16540515 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20200310 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:16540515 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20200310 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0005331 insulin resistance IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:12420138 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20200310 MGI PMID:16540515 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20200310 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20200310 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20200310 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:16540515 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0011124 increased primary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20200310 MGI PMID:16951254 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20200310 MGI PMID:23826075 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20808952 1623920 Kmt2b lysine (K)-specific methyltransferase 2B gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:20808952 1623921 Arhgap36 Rho GTPase activating protein 36 gene MP:0009684 abnormal spinal cord lateral motor column morphology IAGP N RGD:5509061 20190912 MGI PMID:31305241 1623925 Ccdc3 coiled-coil domain containing 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20160310 MGI PMID:25605713 1623925 Ccdc3 coiled-coil domain containing 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20160310 MGI PMID:25605713 1623925 Ccdc3 coiled-coil domain containing 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20160310 MGI PMID:25605713 1623925 Ccdc3 coiled-coil domain containing 3 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20160310 MGI PMID:25605713 1623925 Ccdc3 coiled-coil domain containing 3 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20160310 MGI PMID:25605713 1623925 Ccdc3 coiled-coil domain containing 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20160310 MGI PMID:25605713 1623925 Ccdc3 coiled-coil domain containing 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20160310 MGI PMID:25605713 1623925 Ccdc3 coiled-coil domain containing 3 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20160310 MGI PMID:25605713 1623925 Ccdc3 coiled-coil domain containing 3 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20160310 MGI PMID:25605713 1623925 Ccdc3 coiled-coil domain containing 3 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20170615 MGI PMID:25605713 1623925 Ccdc3 coiled-coil domain containing 3 gene MP:0031270 decreased susceptibility to age-related hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:25605713 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20201022 MGI 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20240321 MGI PMID:38238601 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20240321 MGI PMID:38238601 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20201022 MGI 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20240321 MGI PMID:38238601 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0005376 homeostasis/metabolism phenotype IAGP N RGD:5509061 20240321 MGI PMID:38238601 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200514 MGI 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0014068 abnormal muscle glycogen level IAGP N RGD:5509061 20240321 MGI PMID:38238601 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0021131 increased glycerophosphocholine level IAGP N RGD:5509061 20240321 MGI PMID:38238601 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20240321 MGI PMID:38238601 1623926 Gpcpd1 glycerophosphocholine phosphodiesterase 1 gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20240321 MGI PMID:38238601 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210520 MGI 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240627 MGI 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0005576 decreased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0008691 decreased interleukin-23 secretion IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0012549 hypoxemia IAGP N RGD:5509061 20141003 MGI PMID:24317696 1623927 Muc5b mucin 5, subtype B, tracheobronchial gene MP:0030410 middle ear effusion IAGP N RGD:5509061 20171207 MGI PMID:24317696 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20230601 MGI 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20230601 MGI 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20230601 MGI 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20170831 MGI PMID:26644582 1623929 Zdhhc16 zinc finger, DHHC domain containing 16 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230601 MGI 1623931 Krt80 keratin 80 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1623931 Krt80 keratin 80 gene MP:0001314 cornea opacity IEA N RGD:5509061 20201022 MGI 1623931 Krt80 keratin 80 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1623931 Krt80 keratin 80 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 1623931 Krt80 keratin 80 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 1623932 Cep55 centrosomal protein 55 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210826 MGI 1623932 Cep55 centrosomal protein 55 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0000433 microcephaly IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 1623932 Cep55 centrosomal protein 55 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0002637 small uterus IEA N RGD:5509061 20210826 MGI 1623932 Cep55 centrosomal protein 55 gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 1623932 Cep55 centrosomal protein 55 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0003707 increased cell nucleus count IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0003717 pallor IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 1623932 Cep55 centrosomal protein 55 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 1623932 Cep55 centrosomal protein 55 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0013213 abnormal embryonic neuroepithelium primary cilium morphology IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0013289 abnormal mitotic cytokinesis IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0020382 increased kidney epithelial cell primary cilium length IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623932 Cep55 centrosomal protein 55 gene MP:0020600 decreased cerebral cortex cell density IAGP N RGD:5509061 20201015 MGI PMID:32269212 1623932 Cep55 centrosomal protein 55 gene MP:0030965 increased brain ependyma motile cilium length IAGP N RGD:5509061 20240314 MGI PMID:33475699 1623933 Nebl nebulette gene MP:0000274 enlarged heart IAGP N RGD:5509061 20210610 MGI PMID:33861145 1623933 Nebl nebulette gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20210610 MGI PMID:33861145 1623933 Nebl nebulette gene MP:0002160 abnormal reproductive system morphology IEA N RGD:5509061 20181227 MGI 1623933 Nebl nebulette gene MP:0004063 dilated heart left atrium IAGP N RGD:5509061 20210610 MGI PMID:33861145 1623933 Nebl nebulette gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20210610 MGI PMID:33861145 1623933 Nebl nebulette gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20210610 MGI PMID:33861145 1623933 Nebl nebulette gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20210610 MGI PMID:33861145 1623933 Nebl nebulette gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20210610 MGI PMID:33861145 1623933 Nebl nebulette gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20210610 MGI PMID:33861145 1623933 Nebl nebulette gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20210610 MGI PMID:33861145 1623933 Nebl nebulette gene MP:0020419 decreased cardiac muscle relaxation IAGP N RGD:5509061 20210610 MGI PMID:33861145 1623934 Arpp21 cyclic AMP-regulated phosphoprotein, 21 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20200310 MGI PMID:15499021 1623935 Macrod2 mono-ADP ribosylhydrolase 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230601 MGI 1623935 Macrod2 mono-ADP ribosylhydrolase 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 1623935 Macrod2 mono-ADP ribosylhydrolase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:30619475 1623935 Macrod2 mono-ADP ribosylhydrolase 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210520 MGI 1623935 Macrod2 mono-ADP ribosylhydrolase 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 1623935 Macrod2 mono-ADP ribosylhydrolase 2 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210520 MGI 1623935 Macrod2 mono-ADP ribosylhydrolase 2 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20160421 MGI 1623935 Macrod2 mono-ADP ribosylhydrolase 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1623935 Macrod2 mono-ADP ribosylhydrolase 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1623937 Bbof1 basal body orientation factor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20231102 MGI PMID:37494937 1623937 Bbof1 basal body orientation factor 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20231102 MGI PMID:37494937 1623937 Bbof1 basal body orientation factor 1 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20231102 MGI PMID:37494937 1623937 Bbof1 basal body orientation factor 1 gene MP:0013209 abnormal motile cilium physiology IAGP N RGD:5509061 20231102 MGI PMID:37494937 1623937 Bbof1 basal body orientation factor 1 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20231102 MGI PMID:37494937 1623939 Kctd17 potassium channel tetramerisation domain containing 17 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20200310 MGI 1623940 Pot1b protection of telomeres 1B gene MP:0000175 absent bone marrow cell IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16839877 1623940 Pot1b protection of telomeres 1B gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0002399 abnormal pluripotent precursor cell morphology IEA N RGD:5509061 20111116 MGI 1623940 Pot1b protection of telomeres 1B gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18936156 1623940 Pot1b protection of telomeres 1B gene MP:0011087 neonatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 1623940 Pot1b protection of telomeres 1B gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:18936156 1623941 Pard3b par-3 family cell polarity regulator beta gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 1623941 Pard3b par-3 family cell polarity regulator beta gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 1623941 Pard3b par-3 family cell polarity regulator beta gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20211021 MGI 1623941 Pard3b par-3 family cell polarity regulator beta gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 1623943 Isx intestine specific homeobox gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16971476 1623948 Afmid arylformamidase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20151231 MGI PMID:26432886 1623948 Afmid arylformamidase gene MP:0001426 polydipsia IAGP N RGD:5509061 20151231 MGI PMID:26432886 1623948 Afmid arylformamidase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20151231 MGI PMID:26432886 1623948 Afmid arylformamidase gene MP:0001762 polyuria IAGP N RGD:5509061 20151231 MGI PMID:26432886 1623948 Afmid arylformamidase gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 1623948 Afmid arylformamidase gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20151231 MGI PMID:26432886 1623948 Afmid arylformamidase gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20151231 MGI PMID:26432886 1623948 Afmid arylformamidase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20151231 MGI PMID:26432886 1623948 Afmid arylformamidase gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20151231 MGI PMID:26432886 1623948 Afmid arylformamidase gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 1623948 Afmid arylformamidase gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20151231 MGI PMID:26432886 1623948 Afmid arylformamidase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20151231 MGI PMID:26432886 1623948 Afmid arylformamidase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 1623948 Afmid arylformamidase gene MP:0010087 increased circulating fructosamine level IAGP N RGD:5509061 20151231 MGI PMID:26432886 1623948 Afmid arylformamidase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10029690 1623948 Afmid arylformamidase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10029690 1623949 Arhgap42 Rho GTPase activating protein 42 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20151224 MGI PMID:24335996 1623949 Arhgap42 Rho GTPase activating protein 42 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20151224 MGI PMID:24335996 1623949 Arhgap42 Rho GTPase activating protein 42 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20151224 MGI PMID:24335996 1623949 Arhgap42 Rho GTPase activating protein 42 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 1623949 Arhgap42 Rho GTPase activating protein 42 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20151224 MGI PMID:24335996 1623949 Arhgap42 Rho GTPase activating protein 42 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20151224 MGI PMID:24335996 1623950 Fam217b family with sequence similarity 217, member B gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 1623950 Fam217b family with sequence similarity 217, member B gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220811 MGI 1623950 Fam217b family with sequence similarity 217, member B gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20221215 MGI 1623950 Fam217b family with sequence similarity 217, member B gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20211021 MGI 1623952 Vps35l VPS35 endosomal protein sorting factor like gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20210311 MGI PMID:31712251 1623954 Gcc2 GRIP and coiled-coil domain containing 2 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20240502 MGI PMID:36379959 1623955 Afap1 actin filament associated protein 1 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20160218 MGI PMID:25043309 1623955 Afap1 actin filament associated protein 1 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20160218 MGI PMID:25043309 1623955 Afap1 actin filament associated protein 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20160218 MGI PMID:25043309 1623955 Afap1 actin filament associated protein 1 gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20160218 MGI PMID:25043309 1623955 Afap1 actin filament associated protein 1 gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20160218 MGI PMID:25043309 1623955 Afap1 actin filament associated protein 1 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20160218 MGI PMID:25043309 1623955 Afap1 actin filament associated protein 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20160218 MGI PMID:25043309 1623959 Rnf168 ring finger protein 168 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20210520 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20210826 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20200514 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210520 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210520 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0001262 decreased body weight IEA N RGD:5509061 20210826 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0001307 fused cornea and lens IEA N RGD:5509061 20210826 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210826 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0001314 cornea opacity IEA N RGD:5509061 20201022 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210826 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200514 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210826 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210826 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20210826 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20210520 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20210520 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220519 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20210826 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0005287 narrow eye opening IEA N RGD:5509061 20201022 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0008759 abnormal T cell receptor delta chain V(D)J recombination IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623959 Rnf168 ring finger protein 168 gene MP:0011971 increased circulating lactate dehydrogenase level IEA N RGD:5509061 20211021 MGI 1623959 Rnf168 ring finger protein 168 gene MP:0014127 increased thymoma incidence IAGP N RGD:5509061 20200310 MGI PMID:21552324 1623960 Poc1a POC1 centriolar protein A gene MP:0001116 small gonad IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0001513 limb grasping IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1623960 Poc1a POC1 centriolar protein A gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0002959 increased urine microalbumin level IEA N RGD:5509061 20211021 MGI 1623960 Poc1a POC1 centriolar protein A gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0004708 short lumbar vertebrae IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0005159 azoospermia IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:15177549 1623960 Poc1a POC1 centriolar protein A gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1623960 Poc1a POC1 centriolar protein A gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 1623965 Med27 mediator complex subunit 27 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 1623965 Med27 mediator complex subunit 27 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623966 Tamm41 TAM41 mitochondrial translocator assembly and maintenance homolog gene MP:0008762 embryonic lethality IEA N RGD:5509061 20160728 MGI 1623966 Tamm41 TAM41 mitochondrial translocator assembly and maintenance homolog gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20160804 MGI 1623967 Dcaf12 DDB1 and CUL4 associated factor 12 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1623967 Dcaf12 DDB1 and CUL4 associated factor 12 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 1623967 Dcaf12 DDB1 and CUL4 associated factor 12 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20220811 MGI 1623967 Dcaf12 DDB1 and CUL4 associated factor 12 gene MP:0005655 increased aggression IEA N RGD:5509061 20200514 MGI 1623967 Dcaf12 DDB1 and CUL4 associated factor 12 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20210826 MGI 1623967 Dcaf12 DDB1 and CUL4 associated factor 12 gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20240523 MGI 1623968 Cdan1 codanin 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1623968 Cdan1 codanin 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1623968 Cdan1 codanin 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20181227 MGI 1623968 Cdan1 codanin 1 gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 1623968 Cdan1 codanin 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190808 MGI 1623968 Cdan1 codanin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21364188 1623968 Cdan1 codanin 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 1623968 Cdan1 codanin 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 1623968 Cdan1 codanin 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1623968 Cdan1 codanin 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21364188 1623968 Cdan1 codanin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 1623968 Cdan1 codanin 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1623968 Cdan1 codanin 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1623968 Cdan1 codanin 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20220519 MGI 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20181227 MGI 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20181227 MGI 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20220519 MGI 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0011939 increased food intake IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0014344 abnormal skeletal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20221215 MGI 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623973 Aspscr1 ASPSCR1 tether for SLC2A4, UBX domain containing gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240620 MGI PMID:33686286 1623977 Ift74 intraflagellar transport 74 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 1623977 Ift74 intraflagellar transport 74 gene MP:0001513 limb grasping IEA N RGD:5509061 20201231 MGI 1623977 Ift74 intraflagellar transport 74 gene MP:0001925 male infertility IAGP N RGD:5509061 20220217 MGI PMID:31004481 1623977 Ift74 intraflagellar transport 74 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220217 MGI PMID:31004481 1623977 Ift74 intraflagellar transport 74 gene MP:0002132 abnormal respiratory system morphology IEA N RGD:5509061 20141003 MGI 1623977 Ift74 intraflagellar transport 74 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220217 MGI PMID:31004481 1623977 Ift74 intraflagellar transport 74 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220217 MGI PMID:31004481 1623977 Ift74 intraflagellar transport 74 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220217 MGI PMID:31004481 1623977 Ift74 intraflagellar transport 74 gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 1623977 Ift74 intraflagellar transport 74 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20220217 MGI PMID:31004481 1623977 Ift74 intraflagellar transport 74 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220217 MGI PMID:31004481 1623977 Ift74 intraflagellar transport 74 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220217 MGI PMID:31004481 1623977 Ift74 intraflagellar transport 74 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20141003 MGI 1623977 Ift74 intraflagellar transport 74 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220217 MGI PMID:31004481 1623977 Ift74 intraflagellar transport 74 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20220217 MGI PMID:31004481 1623977 Ift74 intraflagellar transport 74 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220217 MGI PMID:31004481 1623977 Ift74 intraflagellar transport 74 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220217 MGI PMID:31004481 1623977 Ift74 intraflagellar transport 74 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20220217 MGI PMID:31004481 1623977 Ift74 intraflagellar transport 74 gene MP:0010406 common atrium IEA N RGD:5509061 20141003 MGI 1623977 Ift74 intraflagellar transport 74 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1623977 Ift74 intraflagellar transport 74 gene MP:0010975 abnormal lung lobe morphology IEA N RGD:5509061 20141003 MGI 1623977 Ift74 intraflagellar transport 74 gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 1623977 Ift74 intraflagellar transport 74 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220217 MGI PMID:31004481 1623977 Ift74 intraflagellar transport 74 gene MP:0031352 absent sperm axonemal central pair IAGP N RGD:5509061 20220811 MGI PMID:31004481 1623980 Hikeshi heat shock protein nuclear import factor gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1623980 Hikeshi heat shock protein nuclear import factor gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:16157679 1623980 Hikeshi heat shock protein nuclear import factor gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:16157679 1623980 Hikeshi heat shock protein nuclear import factor gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:16157679 1623980 Hikeshi heat shock protein nuclear import factor gene MP:0010809 abnormal club cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16157679 1623980 Hikeshi heat shock protein nuclear import factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16157679 1623980 Hikeshi heat shock protein nuclear import factor gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10224267 1623980 Hikeshi heat shock protein nuclear import factor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16157679 1623980 Hikeshi heat shock protein nuclear import factor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8358168 1623982 Spaca1 sperm acrosome associated 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22949614 1623982 Spaca1 sperm acrosome associated 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22949614 1623982 Spaca1 sperm acrosome associated 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22949614 1623982 Spaca1 sperm acrosome associated 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22949614 1623982 Spaca1 sperm acrosome associated 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22949614 1623982 Spaca1 sperm acrosome associated 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:22949614 1623982 Spaca1 sperm acrosome associated 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:22949614 1623982 Spaca1 sperm acrosome associated 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:22949614 1623982 Spaca1 sperm acrosome associated 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:22949614 1623982 Spaca1 sperm acrosome associated 1 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:22949614 1623983 4930522H14Rik RIKEN cDNA 4930522H14 gene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 1623987 Mxra7 matrix-remodelling associated 7 gene MP:0002764 short tibia IEA N RGD:5509061 20160421 MGI 1623987 Mxra7 matrix-remodelling associated 7 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 1623988 Aasdhppt aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase gene MP:0005102 abnormal iris pigmentation IEA N RGD:5509061 20201022 MGI 1623988 Aasdhppt aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 1623988 Aasdhppt aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1623988 Aasdhppt aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 1623988 Aasdhppt aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623988 Aasdhppt aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1623989 Fibin fin bud initiation factor homolog (zebrafish) gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 1623990 Necap1 NECAP endocytosis associated 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 1623991 Tsfm Ts translation elongation factor, mitochondrial gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 1623991 Tsfm Ts translation elongation factor, mitochondrial gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1623993 Ahnak AHNAK nucleoprotein gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 1623993 Ahnak AHNAK nucleoprotein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:21094140 1623993 Ahnak AHNAK nucleoprotein gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20200310 MGI PMID:18191595 1623993 Ahnak AHNAK nucleoprotein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:15373775 1623993 Ahnak AHNAK nucleoprotein gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20200310 MGI PMID:18191595 1623993 Ahnak AHNAK nucleoprotein gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:18191595 1623993 Ahnak AHNAK nucleoprotein gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 1623993 Ahnak AHNAK nucleoprotein gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20200310 MGI PMID:18191595 1623993 Ahnak AHNAK nucleoprotein gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200310 MGI PMID:21094140 1623993 Ahnak AHNAK nucleoprotein gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:18191595 1623993 Ahnak AHNAK nucleoprotein gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20200310 MGI PMID:18191595 1623993 Ahnak AHNAK nucleoprotein gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20200310 MGI PMID:18191595 1623993 Ahnak AHNAK nucleoprotein gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20200310 MGI PMID:21094140 1623993 Ahnak AHNAK nucleoprotein gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1623993 Ahnak AHNAK nucleoprotein gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 1623998 2310011J03Rik RIKEN cDNA 2310011J03 gene gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 1623998 2310011J03Rik RIKEN cDNA 2310011J03 gene gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20241003 MGI 1623998 2310011J03Rik RIKEN cDNA 2310011J03 gene gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20241003 MGI 1623998 2310011J03Rik RIKEN cDNA 2310011J03 gene gene MP:0001698 decreased embryo size IEA N RGD:5509061 20241003 MGI 1623998 2310011J03Rik RIKEN cDNA 2310011J03 gene gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20241003 MGI 1623998 2310011J03Rik RIKEN cDNA 2310011J03 gene gene MP:0009331 absent primitive node IEA N RGD:5509061 20241003 MGI 1623998 2310011J03Rik RIKEN cDNA 2310011J03 gene gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 1623998 2310011J03Rik RIKEN cDNA 2310011J03 gene gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 1623998 2310011J03Rik RIKEN cDNA 2310011J03 gene gene MP:0012724 absent head fold IEA N RGD:5509061 20241003 MGI 1623999 Chmp4c charged multivesicular body protein 4C gene MP:0002607 decreased basophil cell number IEA N RGD:5509061 20201022 MGI 1623999 Chmp4c charged multivesicular body protein 4C gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1624002 Riiad1 regulatory subunit of type II PKA R-subunit (RIIa) domain containing 1 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20170105 MGI 1624002 Riiad1 regulatory subunit of type II PKA R-subunit (RIIa) domain containing 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20170105 MGI 1624002 Riiad1 regulatory subunit of type II PKA R-subunit (RIIa) domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 1624006 Psenen presenilin enhancer gamma secretase subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200310 MGI 1624008 Fam229b family with sequence similarity 229, member B gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 1624008 Fam229b family with sequence similarity 229, member B gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20240523 MGI 1624008 Fam229b family with sequence similarity 229, member B gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201022 MGI PMID:32588039 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0000416 sparse hair IAGP N RGD:5509061 20230831 MGI PMID:37369199 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20231207 MGI 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0000774 decreased brain size IAGP N RGD:5509061 20230831 MGI PMID:37369199 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20181227 MGI 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20230831 MGI PMID:37369199 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20181227 MGI 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20230831 MGI PMID:37369199 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20230831 MGI PMID:37369199 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0002833 increased heart weight IEA N RGD:5509061 20201022 MGI 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20230831 MGI PMID:37369199 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20230831 MGI PMID:37369199 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20230831 MGI PMID:37369199 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1624013 Mplkip M-phase specific PLK1 intereacting protein gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20230831 MGI PMID:37369199 1624016 Eid1 EP300 interacting inhibitor of differentiation 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20210513 MGI PMID:30926163 1624016 Eid1 EP300 interacting inhibitor of differentiation 1 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20210513 MGI PMID:30926163 1624016 Eid1 EP300 interacting inhibitor of differentiation 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20210513 MGI PMID:30926163 1624016 Eid1 EP300 interacting inhibitor of differentiation 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20210513 MGI PMID:30926163 1624016 Eid1 EP300 interacting inhibitor of differentiation 1 gene MP:0012207 decreased neuronal stem cell self-renewal IAGP N RGD:5509061 20210513 MGI PMID:30926163 1624016 Eid1 EP300 interacting inhibitor of differentiation 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20210513 MGI PMID:30926163 1624017 Bcam basal cell adhesion molecule gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20200310 MGI PMID:18032551 1624017 Bcam basal cell adhesion molecule gene MP:0001260 increased body weight IAGP N RGD:5509061 20200310 MGI PMID:18032551 1624017 Bcam basal cell adhesion molecule gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20200310 MGI 1624017 Bcam basal cell adhesion molecule gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20200310 MGI PMID:18032551 1624017 Bcam basal cell adhesion molecule gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20200310 MGI PMID:18032551 1624017 Bcam basal cell adhesion molecule gene MP:0006087 increased body mass index IAGP N RGD:5509061 20200310 MGI PMID:18032551 1624017 Bcam basal cell adhesion molecule gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20200310 MGI PMID:18032551 1624018 Retnla resistin like alpha gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200310 MGI PMID:19349464 1624018 Retnla resistin like alpha gene MP:0002497 increased IgE level IAGP N RGD:5509061 20200310 MGI PMID:19349464 1624018 Retnla resistin like alpha gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:19201890 1624018 Retnla resistin like alpha gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20200310 MGI PMID:19349464 1624018 Retnla resistin like alpha gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20200310 MGI PMID:19201890 1624018 Retnla resistin like alpha gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20200310 MGI PMID:19349464 1624018 Retnla resistin like alpha gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20200310 MGI PMID:19084112 1624018 Retnla resistin like alpha gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20200310 MGI PMID:19201890 1624018 Retnla resistin like alpha gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20200310 MGI PMID:19084112 1624018 Retnla resistin like alpha gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20200310 MGI PMID:19349464 1624018 Retnla resistin like alpha gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20200310 MGI PMID:19349464 1624018 Retnla resistin like alpha gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20200310 MGI PMID:19349464 1624018 Retnla resistin like alpha gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20200310 MGI PMID:19201890 1624018 Retnla resistin like alpha gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20200310 MGI PMID:19084112 1624018 Retnla resistin like alpha gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20200310 MGI PMID:19201890 1624018 Retnla resistin like alpha gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20200310 MGI PMID:19201890 1624019 Prss21 serine protease 21 gene MP:0000160 kyphosis IEA N RGD:5509061 20230601 MGI 1624019 Prss21 serine protease 21 gene MP:0000162 lordosis IEA N RGD:5509061 20231207 MGI 1624019 Prss21 serine protease 21 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:18754795 1624019 Prss21 serine protease 21 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:19571264 1624019 Prss21 serine protease 21 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 1624019 Prss21 serine protease 21 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 1624019 Prss21 serine protease 21 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 1624019 Prss21 serine protease 21 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 1624019 Prss21 serine protease 21 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 1624019 Prss21 serine protease 21 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 1624019 Prss21 serine protease 21 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19571264 1624019 Prss21 serine protease 21 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19571264 1624019 Prss21 serine protease 21 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20231207 MGI 1624019 Prss21 serine protease 21 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:18754795 1624019 Prss21 serine protease 21 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:19571264 1624019 Prss21 serine protease 21 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19571264 1624019 Prss21 serine protease 21 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:19571264 1624019 Prss21 serine protease 21 gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:19571264 1624019 Prss21 serine protease 21 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:19571264 1624019 Prss21 serine protease 21 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:19571264 1624019 Prss21 serine protease 21 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:19571264 1624019 Prss21 serine protease 21 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:19571264 1624019 Prss21 serine protease 21 gene MP:0009709 hydrometra IEA N RGD:5509061 20210826 MGI 1624019 Prss21 serine protease 21 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 1624019 Prss21 serine protease 21 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220714 MGI PMID:19571264 1624019 Prss21 serine protease 21 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:18754795 1624019 Prss21 serine protease 21 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:18754795 1624020 Cldn13 claudin 13 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20181227 MGI 1624020 Cldn13 claudin 13 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 1624020 Cldn13 claudin 13 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 1624020 Cldn13 claudin 13 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 1624020 Cldn13 claudin 13 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220519 MGI 1624020 Cldn13 claudin 13 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20160421 MGI 1624020 Cldn13 claudin 13 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 1624020 Cldn13 claudin 13 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1624020 Cldn13 claudin 13 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 1624020 Cldn13 claudin 13 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 1624020 Cldn13 claudin 13 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1624020 Cldn13 claudin 13 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 1624024 Ctps2 cytidine 5'-triphosphate synthase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240627 MGI PMID:38438357 1624024 Ctps2 cytidine 5'-triphosphate synthase 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 1624024 Ctps2 cytidine 5'-triphosphate synthase 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20240627 MGI PMID:38438357 1624025 Rp9 retinitis pigmentosa 9 (human) gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 1624025 Rp9 retinitis pigmentosa 9 (human) gene MP:0001258 decreased body length IEA N RGD:5509061 20181227 MGI 1624025 Rp9 retinitis pigmentosa 9 (human) gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20221215 MGI 1624025 Rp9 retinitis pigmentosa 9 (human) gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 1624025 Rp9 retinitis pigmentosa 9 (human) gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 1624027 Ccdc120 coiled-coil domain containing 120 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 1624027 Ccdc120 coiled-coil domain containing 120 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20210826 MGI 1624027 Ccdc120 coiled-coil domain containing 120 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210826 MGI 1624027 Ccdc120 coiled-coil domain containing 120 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 1624028 Gripap1 GRIP1 associated protein 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20180607 MGI PMID:28285821 1624028 Gripap1 GRIP1 associated protein 1 gene MP:0003247 abnormal glutaminergic neuron morphology IAGP N RGD:5509061 20180607 MGI PMID:28285821 1624028 Gripap1 GRIP1 associated protein 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20180607 MGI PMID:28285821 1624028 Gripap1 GRIP1 associated protein 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20180607 MGI PMID:28285821 1624028 Gripap1 GRIP1 associated protein 1 gene MP:0012293 impaired active avoidance behavior IAGP N RGD:5509061 20180607 MGI PMID:28285821 1624028 Gripap1 GRIP1 associated protein 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20180607 MGI PMID:28285821 1624029 Otud5 OTU domain containing 5 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20170518 MGI PMID:25470037 1624029 Otud5 OTU domain containing 5 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20111116 MGI 1624029 Otud5 OTU domain containing 5 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20170518 MGI PMID:25470037 1624029 Otud5 OTU domain containing 5 gene MP:0002084 abnormal developmental patterning IEA N RGD:5509061 20111116 MGI 1624029 Otud5 OTU domain containing 5 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20170518 MGI PMID:25470037 1624029 Otud5 OTU domain containing 5 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20170518 MGI PMID:25470037 1624029 Otud5 OTU domain containing 5 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20170518 MGI PMID:25470037 1624029 Otud5 OTU domain containing 5 gene MP:0008711 increased interleukin-9 secretion IAGP N RGD:5509061 20170518 MGI PMID:25470037 1624029 Otud5 OTU domain containing 5 gene MP:0009057 increased interleukin-21 secretion IAGP N RGD:5509061 20170518 MGI PMID:25470037 1624029 Otud5 OTU domain containing 5 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20170518 MGI PMID:25470037 1624029 Otud5 OTU domain containing 5 gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20170518 MGI PMID:25470037 1624031 Tbc1d8 TBC1 domain family, member 8 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 1624031 Tbc1d8 TBC1 domain family, member 8 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 1624031 Tbc1d8 TBC1 domain family, member 8 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 1624032 Rab11fip5 RAB11 family interacting protein 5 (class I) gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 1624032 Rab11fip5 RAB11 family interacting protein 5 (class I) gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 1624032 Rab11fip5 RAB11 family interacting protein 5 (class I) gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 1624034 Pibf1 progesterone immunomodulatory binding factor 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 1624034 Pibf1 progesterone immunomodulatory binding factor 1 gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20170105 MGI 1624034 Pibf1 progesterone immunomodulatory binding factor 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20170105 MGI 1624034 Pibf1 progesterone immunomodulatory binding factor 1 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20170105 MGI 1624034 Pibf1 progesterone immunomodulatory binding factor 1 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20170105 MGI 1624034 Pibf1 progesterone immunomodulatory binding factor 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 1624034 Pibf1 progesterone immunomodulatory binding factor 1 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20170105 MGI 1624034 Pibf1 progesterone immunomodulatory binding factor 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 1624034 Pibf1 progesterone immunomodulatory binding factor 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 1624034 Pibf1 progesterone immunomodulatory binding factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1624034 Pibf1 progesterone immunomodulatory binding factor 1 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20220519 MGI 1624034 Pibf1 progesterone immunomodulatory binding factor 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1624035 Umodl1 uromodulin-like 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 1624036 Cdk2ap2 cyclin dependent kinase 2 associated protein 2 gene MP:0001304 cataract IEA N RGD:5509061 20200310 MGI 1624036 Cdk2ap2 cyclin dependent kinase 2 associated protein 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1624036 Cdk2ap2 cyclin dependent kinase 2 associated protein 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220519 MGI 1624036 Cdk2ap2 cyclin dependent kinase 2 associated protein 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 1624039 Fbxo15 F-box protein 15 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12665572 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21503901 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180531 MGI PMID:29386660 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:14672936 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:17984302 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:14766969 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:18474632 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:17984302 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20935640 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:21827743 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:20935640 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:21827743 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21827743 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21827743 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:21827743 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:14766969 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:20935640 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:14766969 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001147 small testis IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20180531 MGI PMID:29386660 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20240704 MGI PMID:21503901 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:21503901 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20180531 MGI PMID:29386660 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001586 abnormal erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14766969 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:14766969 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:14672936 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:14672936 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14766969 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:14766969 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:14766969 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:14672936 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18474632 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17984302 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:17984302 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14672936 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20180531 MGI PMID:29386660 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17984302 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18474632 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20935640 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17984302 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20180531 MGI PMID:29386660 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18474632 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23791182 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17984302 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20935640 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20180531 MGI PMID:29386660 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:14672936 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:14672936 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14672936 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14766969 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:14672936 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20935640 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:18474632 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23791182 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20180531 MGI PMID:29386660 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0004930 small epididymis IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:14672936 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:20935640 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:18474632 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17984302 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14672936 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:21503901 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20141003 MGI PMID:20935640 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17984302 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0006428 ectopic Sertoli cells IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17984302 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20935640 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20935640 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20141003 MGI PMID:21827743 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:20935640 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21827743 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:23791182 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20180531 MGI PMID:29386660 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23791182 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21503901 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180531 MGI PMID:29386660 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17984302 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21827743 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14672936 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14766969 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23791182 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17984302 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0012728 abnormal somite border morphology IAGP N RGD:5509061 20141003 MGI PMID:14672936 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:21827743 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0020355 abnormal Sertoli cell barrier morphology IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20220616 MGI PMID:31883011 1624041 Fbxw7 F-box and WD-40 domain protein 7 gene MP:0020528 thalamus hypoplasia IAGP N RGD:5509061 20180208 MGI PMID:20935640 1624042 Dkkl1 dickkopf-like 1 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18818293 1624042 Dkkl1 dickkopf-like 1 gene MP:0005411 delayed fertilization IAGP N RGD:5509061 20141003 MGI PMID:19596312 1624042 Dkkl1 dickkopf-like 1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20220714 MGI PMID:18818293 1624042 Dkkl1 dickkopf-like 1 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:19596312 1624042 Dkkl1 dickkopf-like 1 gene MP:0030603 increased sperm number IAGP N RGD:5509061 20220714 MGI PMID:18818293 1624042 Dkkl1 dickkopf-like 1 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:19596312 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11689686 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160204 MGI PMID:23633960 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624043 H1f4 H1.4 linker histone, cluster member gene MP:0012156 rostral-caudal axis duplication IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11689686 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160204 MGI PMID:23633960 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0004587 decreased cellular sensitivity to X-ray irradiation IAGP N RGD:5509061 20141003 MGI PMID:14505568 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624044 H1f2 H1.2 linker histone, cluster member gene MP:0012156 rostral-caudal axis duplication IAGP N RGD:5509061 20141003 MGI PMID:12808097 1624045 Elane elastase, neutrophil expressed gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14636558 1624045 Elane elastase, neutrophil expressed gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14975240 1624045 Elane elastase, neutrophil expressed gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16872848 1624045 Elane elastase, neutrophil expressed gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20191226 MGI PMID:25915831 1624045 Elane elastase, neutrophil expressed gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:14636558 1624045 Elane elastase, neutrophil expressed gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12384420 1624045 Elane elastase, neutrophil expressed gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:14975240 1624045 Elane elastase, neutrophil expressed gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9585238 1624045 Elane elastase, neutrophil expressed gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:14975240 1624045 Elane elastase, neutrophil expressed gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:9585238 1624045 Elane elastase, neutrophil expressed gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:14975240 1624045 Elane elastase, neutrophil expressed gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20191226 MGI PMID:25915831 1624045 Elane elastase, neutrophil expressed gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:10714686 1624045 Elane elastase, neutrophil expressed gene MP:0008561 decreased tumor necrosis factor secretion IEA N RGD:5509061 20150402 MGI 1624045 Elane elastase, neutrophil expressed gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18568075 1624045 Elane elastase, neutrophil expressed gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:10714686 1624045 Elane elastase, neutrophil expressed gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:14633606 1624045 Elane elastase, neutrophil expressed gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16754715 1624045 Elane elastase, neutrophil expressed gene MP:0009787 increased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10714686 1624045 Elane elastase, neutrophil expressed gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9585238 1624045 Elane elastase, neutrophil expressed gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10714686 1624045 Elane elastase, neutrophil expressed gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9585238 1624046 Mrpl39 mitochondrial ribosomal protein L39 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20240523 MGI 1624046 Mrpl39 mitochondrial ribosomal protein L39 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20240523 MGI 1624046 Mrpl39 mitochondrial ribosomal protein L39 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 1624046 Mrpl39 mitochondrial ribosomal protein L39 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 1624054 Defb3 defensin beta 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23670560 1624054 Defb3 defensin beta 3 gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:23670560 1624054 Defb3 defensin beta 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21115716 1624054 Defb3 defensin beta 3 gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:23670560 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20240307 MGI PMID:29133847 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20240307 MGI PMID:29133847 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20240307 MGI PMID:29133847 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0002309 abnormal vital capacity IAGP N RGD:5509061 20240307 MGI PMID:29133847 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0002311 abnormal inspiratory capacity IAGP N RGD:5509061 20240307 MGI PMID:29133847 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230601 MGI 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0006057 decreased vascular endothelial cell number IAGP N RGD:5509061 20240307 MGI PMID:29133847 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20230601 MGI 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0009455 enhanced cued conditioning behavior IEA N RGD:5509061 20230601 MGI 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20240307 MGI PMID:29133847 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0010936 decreased airway resistance IAGP N RGD:5509061 20240307 MGI PMID:29133847 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0010937 increased total lung capacity IAGP N RGD:5509061 20240307 MGI PMID:29133847 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0011139 increased lung endothelial cell proliferation IAGP N RGD:5509061 20240307 MGI PMID:29133847 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0011141 increased lung endothelial cell apoptosis IAGP N RGD:5509061 20240307 MGI PMID:29133847 1624055 Pald1 phosphatase domain containing, paladin 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 1624057 Ubc ubiquitin C gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:17491588 1624057 Ubc ubiquitin C gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17491588 1624057 Ubc ubiquitin C gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:17491588 1624057 Ubc ubiquitin C gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17491588 1624057 Ubc ubiquitin C gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20201022 MGI 1624057 Ubc ubiquitin C gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:17491588 1624057 Ubc ubiquitin C gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17491588 1624057 Ubc ubiquitin C gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20200402 MGI 1624057 Ubc ubiquitin C gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:17491588 1624057 Ubc ubiquitin C gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17491588 1624057 Ubc ubiquitin C gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17491588 1624057 Ubc ubiquitin C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1624057 Ubc ubiquitin C gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17491588 1624057 Ubc ubiquitin C gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 1624058 Zrsr2 zinc finger (CCCH type), RNA binding motif and serine/arginine rich 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 1624058 Zrsr2 zinc finger (CCCH type), RNA binding motif and serine/arginine rich 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 1624058 Zrsr2 zinc finger (CCCH type), RNA binding motif and serine/arginine rich 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 1624058 Zrsr2 zinc finger (CCCH type), RNA binding motif and serine/arginine rich 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 1624058 Zrsr2 zinc finger (CCCH type), RNA binding motif and serine/arginine rich 2 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 1624058 Zrsr2 zinc finger (CCCH type), RNA binding motif and serine/arginine rich 2 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 1624058 Zrsr2 zinc finger (CCCH type), RNA binding motif and serine/arginine rich 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 1624058 Zrsr2 zinc finger (CCCH type), RNA binding motif and serine/arginine rich 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20210429 MGI PMID:32527007 1624059 Zrsr2-ps1 zinc finger (CCCH type), RNA binding motif and serine/arginine rich 2, pseudogene 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10679248 1624059 Zrsr2-ps1 zinc finger (CCCH type), RNA binding motif and serine/arginine rich 2, pseudogene 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20210429 MGI PMID:32527007 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12569157 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15632019 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:15073337 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:12569157 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:15073337 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:15632019 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:17611620 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15073337 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21841309 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15632019 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:12569157 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15632019 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12569157 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15073337 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:12569157 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:12569157 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:15632019 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:17611620 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:19251634 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:21841309 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15632019 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:15878887 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15878887 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16715077 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0002635 reduced sensorimotor gating IAGP N RGD:5509061 20141003 MGI PMID:12569157 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12569157 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15601948 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12569157 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:15632019 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:17611620 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:15601948 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0003080 increased natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11021532 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:15073337 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20212065 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:21727189 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:15073337 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15878887 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:15878887 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0004260 enlarged placenta IAGP N RGD:5509061 20141003 MGI PMID:15878887 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21727189 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:11021532 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:12569157 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:21841309 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:21841309 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:15073337 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:15632019 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:17611620 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:19332875 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11021532 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11021533 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11021532 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21727189 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:12569157 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:15632019 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:15073337 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:15632019 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:17611620 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11021533 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19332875 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:11021532 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:11021533 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:15073337 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21727189 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15632019 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:15073337 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21841309 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:21727189 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:21727189 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:21727189 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:21727189 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11021532 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15878887 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19332875 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21727189 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15601948 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0008876 decreased uterine NK cell number IAGP N RGD:5509061 20141003 MGI PMID:15878887 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:12569157 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:15632019 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:15632019 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:17611620 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:21841309 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:12569157 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:15632019 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:21841309 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0010932 increased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:17611620 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0012529 abnormal decidua basalis morphology IAGP N RGD:5509061 20141003 MGI PMID:15878887 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0012726 abnormal uterine spiral artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15878887 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0012727 abnormal uterine spiral artery remodeling IAGP N RGD:5509061 20141003 MGI PMID:15878887 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:12569157 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:11927627 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0021195 increased bone mineral density of caudal vertebrae IAGP N RGD:5509061 20220922 MGI PMID:12569157 1624060 Tyrobp TYRO protein tyrosine kinase binding protein gene MP:0030072 round face IAGP N RGD:5509061 20170921 MGI PMID:15073337 1624063 Tubb5 tubulin, beta 5 class I gene MP:0000433 microcephaly IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624063 Tubb5 tubulin, beta 5 class I gene MP:0000774 decreased brain size IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624063 Tubb5 tubulin, beta 5 class I gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624063 Tubb5 tubulin, beta 5 class I gene MP:0000852 small cerebellum IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624063 Tubb5 tubulin, beta 5 class I gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624063 Tubb5 tubulin, beta 5 class I gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624063 Tubb5 tubulin, beta 5 class I gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624063 Tubb5 tubulin, beta 5 class I gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624063 Tubb5 tubulin, beta 5 class I gene MP:0004079 abnormal putamen morphology IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624063 Tubb5 tubulin, beta 5 class I gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624063 Tubb5 tubulin, beta 5 class I gene MP:0008283 small hippocampus IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624063 Tubb5 tubulin, beta 5 class I gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624063 Tubb5 tubulin, beta 5 class I gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624063 Tubb5 tubulin, beta 5 class I gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624063 Tubb5 tubulin, beta 5 class I gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624063 Tubb5 tubulin, beta 5 class I gene MP:0020527 small thalamus IAGP N RGD:5509061 20200310 MGI PMID:26903504 1624064 Tuba3a tubulin, alpha 3A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20211021 MGI PMID:34326397 1624064 Tuba3a tubulin, alpha 3A gene MP:0011939 increased food intake IEA N RGD:5509061 20211021 MGI 1624064 Tuba3a tubulin, alpha 3A gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20211021 MGI PMID:34326397 1624066 Ttn titin gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:24470489 1624066 Ttn titin gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0000263 absent organized vascular network IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20210408 MGI PMID:33637999 1624066 Ttn titin gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:19406126 1624066 Ttn titin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16702235 1624066 Ttn titin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23709671 1624066 Ttn titin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20160602 MGI PMID:25246556 1624066 Ttn titin gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17360664 1624066 Ttn titin gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:12464612 1624066 Ttn titin gene MP:0000749 muscle degeneration IEA N RGD:5509061 20111116 MGI 1624066 Ttn titin gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14741210 1624066 Ttn titin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12464612 1624066 Ttn titin gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:12464612 1624066 Ttn titin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12464612 1624066 Ttn titin gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:12464612 1624066 Ttn titin gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19679835 1624066 Ttn titin gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:23709671 1624066 Ttn titin gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16702235 1624066 Ttn titin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19406126 1624066 Ttn titin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12464612 1624066 Ttn titin gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:19406126 1624066 Ttn titin gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12464612 1624066 Ttn titin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14741210 1624066 Ttn titin gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19679835 1624066 Ttn titin gene MP:0002127 abnormal cardiovascular system morphology IEA N RGD:5509061 20111116 MGI 1624066 Ttn titin gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12464612 1624066 Ttn titin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21555460 1624066 Ttn titin gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:16702235 1624066 Ttn titin gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:24470489 1624066 Ttn titin gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19679835 1624066 Ttn titin gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20160602 MGI PMID:25246556 1624066 Ttn titin gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:16702235 1624066 Ttn titin gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:19406126 1624066 Ttn titin gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20210408 MGI PMID:33637999 1624066 Ttn titin gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:19406126 1624066 Ttn titin gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17360664 1624066 Ttn titin gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20160602 MGI PMID:25246556 1624066 Ttn titin gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19679835 1624066 Ttn titin gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:19406126 1624066 Ttn titin gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0003820 increased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:19679835 1624066 Ttn titin gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19406126 1624066 Ttn titin gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23709671 1624066 Ttn titin gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20160602 MGI PMID:25246556 1624066 Ttn titin gene MP:0003923 abnormal heart left atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:23709671 1624066 Ttn titin gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16702235 1624066 Ttn titin gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19406126 1624066 Ttn titin gene MP:0004011 decreased diastolic filling velocity IAGP N RGD:5509061 20141003 MGI PMID:17360664 1624066 Ttn titin gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:19406126 1624066 Ttn titin gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:12464612 1624066 Ttn titin gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:17360664 1624066 Ttn titin gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:19679835 1624066 Ttn titin gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20160602 MGI PMID:25246556 1624066 Ttn titin gene MP:0004094 abnormal M line morphology IAGP N RGD:5509061 20141003 MGI PMID:12464612 1624066 Ttn titin gene MP:0004094 abnormal M line morphology IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:17360664 1624066 Ttn titin gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:19679835 1624066 Ttn titin gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20160602 MGI PMID:25246556 1624066 Ttn titin gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19406126 1624066 Ttn titin gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16702235 1624066 Ttn titin gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16702235 1624066 Ttn titin gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16702235 1624066 Ttn titin gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19406126 1624066 Ttn titin gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20210408 MGI PMID:33637999 1624066 Ttn titin gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19406126 1624066 Ttn titin gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:24470489 1624066 Ttn titin gene MP:0006042 increased apoptosis IEA N RGD:5509061 20150226 MGI 1624066 Ttn titin gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:24470489 1624066 Ttn titin gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0009426 decreased soleus weight IAGP N RGD:5509061 20141003 MGI PMID:24470489 1624066 Ttn titin gene MP:0010225 abnormal quadriceps morphology IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:19679835 1624066 Ttn titin gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16702235 1624066 Ttn titin gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19406126 1624066 Ttn titin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12464612 1624066 Ttn titin gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20855473 1624066 Ttn titin gene MP:0011266 abnormal frontonasal mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:15136139 1624066 Ttn titin gene MP:0011915 increased heart left atrium weight IAGP N RGD:5509061 20141003 MGI PMID:23709671 1624066 Ttn titin gene MP:0011915 increased heart left atrium weight IAGP N RGD:5509061 20160602 MGI PMID:25246556 1624066 Ttn titin gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:23709671 1624066 Ttn titin gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20160602 MGI PMID:25246556 1624066 Ttn titin gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150219 MGI PMID:16702235 1624066 Ttn titin gene MP:0021206 abnormal limb muscle morphology IAGP N RGD:5509061 20221201 MGI PMID:20855473 1624066 Ttn titin gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:33637999 1624068 Tsks testis-specific serine kinase substrate gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20230810 MGI PMID:36881620 1624068 Tsks testis-specific serine kinase substrate gene MP:0001925 male infertility IAGP N RGD:5509061 20230810 MGI PMID:36881620 1624068 Tsks testis-specific serine kinase substrate gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230810 MGI PMID:36881620 1624068 Tsks testis-specific serine kinase substrate gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 1624068 Tsks testis-specific serine kinase substrate gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20230810 MGI PMID:36881620 1624068 Tsks testis-specific serine kinase substrate gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230810 MGI PMID:36881620 1624068 Tsks testis-specific serine kinase substrate gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20230810 MGI PMID:36881620 1624068 Tsks testis-specific serine kinase substrate gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20230810 MGI PMID:36881620 1624068 Tsks testis-specific serine kinase substrate gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20230810 MGI PMID:36881620 1624068 Tsks testis-specific serine kinase substrate gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20230810 MGI PMID:36881620 1624068 Tsks testis-specific serine kinase substrate gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20230810 MGI PMID:36881620 1624068 Tsks testis-specific serine kinase substrate gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20230810 MGI PMID:36881620 1624068 Tsks testis-specific serine kinase substrate gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20230810 MGI PMID:36881620 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0001127 small ovary IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:18799790 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0001147 small testis IAGP N RGD:5509061 20210422 MGI PMID:28914256 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0001147 small testis IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0001924 infertility IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0001925 male infertility IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0001926 female infertility IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20210422 MGI PMID:28914256 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20210422 MGI PMID:28914256 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20210422 MGI PMID:28914256 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:24183939 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:18799790 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210422 MGI PMID:28914256 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:18799790 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0005159 azoospermia IAGP N RGD:5509061 20210107 MGI PMID:32032549 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0005159 azoospermia IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:16461896 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:24183939 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18799790 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:24183939 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20210107 MGI PMID:32032549 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20210422 MGI PMID:28914256 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210422 MGI PMID:28914256 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18799790 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20210107 MGI PMID:32032549 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20210422 MGI PMID:28914256 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20210422 MGI PMID:28914256 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20210422 MGI PMID:28914256 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0013236 ovary degeneration IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20210422 MGI PMID:28914256 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210422 MGI PMID:28914256 1624070 Stra8 stimulated by retinoic acid gene 8 gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20240606 MGI PMID:37439366 1624071 Cenpx centromere protein X gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230119 MGI 1624072 Sult1c1 sulfotransferase family, cytosolic, 1C, member 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 1624074 Stag2 STAG2 cohesin complex component gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0001577 anemia IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0002006 neoplasm IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0002083 premature death IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0005397 hematopoietic system phenotype IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0010406 common atrium IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20210121 MGI PMID:32783938 1624074 Stag2 STAG2 cohesin complex component gene MP:0013658 abnormal myeloid cell morphology IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0013696 increased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0013705 decreased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0013707 abnormal hematopoietic precursor cell morphology IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0013891 increased common myeloid progenitor cell number IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624074 Stag2 STAG2 cohesin complex component gene MP:0013893 decreased common lymphocyte progenitor cell number IAGP N RGD:5509061 20210520 MGI PMID:32249213 1624075 Ro60 Ro60, Y RNA binding protein gene MP:0001202 skin photosensitivity IAGP N RGD:5509061 20200310 MGI PMID:12788971 1624075 Ro60 Ro60, Y RNA binding protein gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:12788971 1624075 Ro60 Ro60, Y RNA binding protein gene MP:0002494 increased IgM level IAGP N RGD:5509061 20200310 MGI PMID:12788971 1624075 Ro60 Ro60, Y RNA binding protein gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20200310 MGI PMID:12788971 1624075 Ro60 Ro60, Y RNA binding protein gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20200310 MGI PMID:12788971 1624075 Ro60 Ro60, Y RNA binding protein gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20200310 MGI PMID:12788971 1624075 Ro60 Ro60, Y RNA binding protein gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200310 MGI PMID:12788971 1624075 Ro60 Ro60, Y RNA binding protein gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20200310 MGI PMID:12788971 1624075 Ro60 Ro60, Y RNA binding protein gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20200310 MGI PMID:12788971 1624075 Ro60 Ro60, Y RNA binding protein gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20200310 MGI PMID:12788971 1624075 Ro60 Ro60, Y RNA binding protein gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20200310 MGI PMID:12788971 1624076 Srprb signal recognition particle receptor, B subunit gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 1624076 Srprb signal recognition particle receptor, B subunit gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210128 MGI 1624076 Srprb signal recognition particle receptor, B subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1624076 Srprb signal recognition particle receptor, B subunit gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 1624076 Srprb signal recognition particle receptor, B subunit gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 1624077 Srms src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristylation sites gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7935409 1624078 Ocln occludin gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20200310 MGI PMID:16679411 1624078 Ocln occludin gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:11102513 1624078 Ocln occludin gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20200310 MGI PMID:11102513 1624078 Ocln occludin gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20200310 MGI PMID:11102513 1624078 Ocln occludin gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20200310 MGI PMID:11102513 1624078 Ocln occludin gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20200310 MGI PMID:11102513 1624078 Ocln occludin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:11102513 1624078 Ocln occludin gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20200310 MGI PMID:11102513 1624078 Ocln occludin gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20200310 MGI PMID:16679411 1624078 Ocln occludin gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:11102513 1624078 Ocln occludin gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20200310 MGI PMID:16679411 1624078 Ocln occludin gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:11102513 1624078 Ocln occludin gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20200310 MGI PMID:11102513 1624078 Ocln occludin gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20200310 MGI PMID:16679411 1624078 Ocln occludin gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20200310 MGI PMID:11102513 1624078 Ocln occludin gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20200310 MGI PMID:16679411 1624078 Ocln occludin gene MP:0005211 increased stomach mucosa thickness IAGP N RGD:5509061 20200310 MGI PMID:11102513 1624078 Ocln occludin gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:11102513 1624078 Ocln occludin gene MP:0009517 abnormal salivary gland duct morphology IAGP N RGD:5509061 20200310 MGI PMID:11102513 1624078 Ocln occludin gene MP:0009517 abnormal salivary gland duct morphology IAGP N RGD:5509061 20200310 MGI PMID:16679411 1624078 Ocln occludin gene MP:0010779 abnormal stomach muscularis externa morphology IAGP N RGD:5509061 20200310 MGI PMID:16679411 1624078 Ocln occludin gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20200310 MGI PMID:16679411 1624079 Oc90 otoconin 90 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16245023 1624079 Oc90 otoconin 90 gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20141003 MGI PMID:17300776 1624079 Oc90 otoconin 90 gene MP:0003143 enlarged otoliths IAGP N RGD:5509061 20141003 MGI PMID:17300776 1624079 Oc90 otoconin 90 gene MP:0003144 decreased otolith number IAGP N RGD:5509061 20141003 MGI PMID:17300776 1624079 Oc90 otoconin 90 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17300776 1624079 Oc90 otoconin 90 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:17300776 1624079 Oc90 otoconin 90 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17300776 1624081 Oaz2 ornithine decarboxylase antizyme 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 1624081 Oaz2 ornithine decarboxylase antizyme 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 1624081 Oaz2 ornithine decarboxylase antizyme 2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 1624081 Oaz2 ornithine decarboxylase antizyme 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0000421 mottled coat IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0000578 ulcerated autopod IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:10681461 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:10681461 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:15247919 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20151231 MGI PMID:24516396 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20231109 MGI PMID:36730190 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0001320 small pupil IAGP N RGD:5509061 20231109 MGI PMID:36730190 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20231109 MGI PMID:36730190 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0001490 abnormal vibrissae reflex IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:15247919 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0002003 miotic pupil IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15247919 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15820690 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:22442072 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15459109 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15459109 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15459109 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0002735 abnormal chemical nociception IAGP N RGD:5509061 20151231 MGI PMID:24516396 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141106 MGI PMID:24623787 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20151231 MGI PMID:24516396 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19755105 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20231109 MGI PMID:36730190 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:22442072 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20231109 MGI PMID:36730190 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0003663 abnormal thermosensation IAGP N RGD:5509061 20141106 MGI PMID:24623787 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0003663 abnormal thermosensation IAGP N RGD:5509061 20151231 MGI PMID:24516396 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141106 MGI PMID:24623787 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15247919 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141106 MGI PMID:24623787 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:22442072 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:15459109 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20151231 MGI PMID:24516396 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0008467 absent proprioceptive neurons IAGP N RGD:5509061 20141003 MGI PMID:15247919 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0008485 increased muscle spindle number IAGP N RGD:5509061 20141003 MGI PMID:15247919 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15459109 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:15459109 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22442072 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0010055 abnormal sensory neuron physiology IAGP N RGD:5509061 20151015 MGI PMID:21199218 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8145823 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1624082 Ntrk1 neurotrophic tyrosine kinase, receptor, type 1 gene MP:0014488 abnormal skin sensory neuron innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:24516396 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20231207 MGI 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0000274 enlarged heart IEA N RGD:5509061 20231207 MGI 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20231207 MGI 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20231207 MGI 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0000691 enlarged spleen IEA N RGD:5509061 20231207 MGI 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20231207 MGI 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20231207 MGI 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0001147 small testis IEA N RGD:5509061 20231207 MGI 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:11038185 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:11038185 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:11038185 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11038185 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20231207 MGI 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:11038185 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:11038185 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0003454 erythroderma IAGP N RGD:5509061 20141003 MGI PMID:11038185 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0003917 increased kidney weight IEA N RGD:5509061 20231207 MGI 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0004906 enlarged uterus IEA N RGD:5509061 20231207 MGI 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0004952 increased spleen weight IEA N RGD:5509061 20231207 MGI 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20231207 MGI 1624083 Loricrin loricrin cornified envelope precursor protein gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 1624084 Lmnb2 lamin B2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:22116031 1624084 Lmnb2 lamin B2 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:22116031 1624084 Lmnb2 lamin B2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:20145110 1624084 Lmnb2 lamin B2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:20145110 1624084 Lmnb2 lamin B2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20145110 1624084 Lmnb2 lamin B2 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:20145110 1624084 Lmnb2 lamin B2 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22116031 1624084 Lmnb2 lamin B2 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20145110 1624084 Lmnb2 lamin B2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:20145110 1624084 Lmnb2 lamin B2 gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:20145110 1624084 Lmnb2 lamin B2 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:20145110 1624084 Lmnb2 lamin B2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22116031 1624084 Lmnb2 lamin B2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:22116031 1624084 Lmnb2 lamin B2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:22116031 1624084 Lmnb2 lamin B2 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21659336 1624084 Lmnb2 lamin B2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:22116031 1624084 Lmnb2 lamin B2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:20145110 1624084 Lmnb2 lamin B2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:22116031 1624084 Lmnb2 lamin B2 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:22116031 1624084 Lmnb2 lamin B2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20141003 MGI 1624084 Lmnb2 lamin B2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22116031 1624084 Lmnb2 lamin B2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:20145110 1624084 Lmnb2 lamin B2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:22116031 1624084 Lmnb2 lamin B2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22116031 1624084 Lmnb2 lamin B2 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20145110 1624084 Lmnb2 lamin B2 gene MP:0009718 absent Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:20145110 1624084 Lmnb2 lamin B2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:22116031 1624084 Lmnb2 lamin B2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20145110 1624084 Lmnb2 lamin B2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22116031 1624084 Lmnb2 lamin B2 gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20141003 MGI PMID:22116031 1624085 G6pd2 glucose-6-phosphate dehydrogenase 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20200310 MGI 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20230601 MGI 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15684394 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0008747 abnormal T cell anergy IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0008838 decreased transforming growth factor beta level IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19592273 1624086 Dtx1 deltex 1, E3 ubiquitin ligase gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:19592273 1624089 Aktip AKT interacting protein gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0000160 kyphosis IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 1624089 Aktip AKT interacting protein gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 1624089 Aktip AKT interacting protein gene MP:0001406 abnormal gait IEA N RGD:5509061 20240523 MGI 1624089 Aktip AKT interacting protein gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0001860 liver inflammation IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0001861 lung inflammation IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0001925 male infertility IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0002083 premature death IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0002188 small heart IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0002764 short tibia IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0003109 short femur IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0004652 small caudal vertebrae IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 1624089 Aktip AKT interacting protein gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0006394 abnormal vertebral epiphyseal plate morphology IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0008409 increased cellular sensitivity to hydroxyurea IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160421 MGI 1624089 Aktip AKT interacting protein gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624089 Aktip AKT interacting protein gene MP:0014040 increased cellular sensitivity to DNA damaging agents IAGP N RGD:5509061 20190711 MGI PMID:29635765 1624090 Ftl2-ps ferritin light polypeptide 2, pseudogene gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200514 MGI 1624090 Ftl2-ps ferritin light polypeptide 2, pseudogene gene MP:0000274 enlarged heart IEA N RGD:5509061 20200514 MGI 1624094 Frk fyn-related kinase gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:12077350 1624096 Cyp2c38 cytochrome P450, family 2, subfamily c, polypeptide 38 gene MP:0001258 decreased body length IEA N RGD:5509061 20230119 MGI 1624096 Cyp2c38 cytochrome P450, family 2, subfamily c, polypeptide 38 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230119 MGI 1624096 Cyp2c38 cytochrome P450, family 2, subfamily c, polypeptide 38 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230119 MGI 1624096 Cyp2c38 cytochrome P450, family 2, subfamily c, polypeptide 38 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 1624098 Cyp2b9 cytochrome P450, family 2, subfamily b, polypeptide 9 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210520 MGI 1624105 Ctla2b cytotoxic T lymphocyte-associated protein 2 beta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170105 MGI 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:16818610 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0001147 small testis IAGP N RGD:5509061 20220120 MGI PMID:31755150 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20220120 MGI PMID:31755150 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220120 MGI PMID:31755150 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16818610 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12529396 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12529396 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0001925 male infertility IAGP N RGD:5509061 20220120 MGI PMID:31755150 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0001926 female infertility IAGP N RGD:5509061 20220120 MGI PMID:29725001 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220120 MGI PMID:31755150 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20220120 MGI PMID:31755150 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12529396 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20220120 MGI PMID:29725001 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:16818610 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220120 MGI PMID:31755150 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220120 MGI PMID:29725001 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220120 MGI PMID:31755150 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:12529396 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12529396 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0005159 azoospermia IAGP N RGD:5509061 20220120 MGI PMID:31755150 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20220120 MGI PMID:29725001 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220120 MGI PMID:31755150 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220120 MGI PMID:31755150 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20220120 MGI PMID:31755150 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16818610 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20220120 MGI PMID:29725001 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12529396 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220120 MGI PMID:29725001 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0011122 absent primordial ovarian follicles IAGP N RGD:5509061 20220120 MGI PMID:29725001 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0011126 absent primary ovarian follicles IAGP N RGD:5509061 20220120 MGI PMID:29725001 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220120 MGI PMID:29725001 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0011130 absent tertiary ovarian follicles IAGP N RGD:5509061 20220120 MGI PMID:29725001 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20220120 MGI PMID:29725001 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20220120 MGI PMID:31755150 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220120 MGI PMID:31755150 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20220120 MGI PMID:29725001 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220120 MGI PMID:29725001 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:29725001 1624107 Csnk2b casein kinase 2, beta polypeptide gene MP:0031382 absent secondary ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:29725001 1624108 Ap3s2 adaptor-related protein complex 3, sigma 2 subunit gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20201022 MGI 1624108 Ap3s2 adaptor-related protein complex 3, sigma 2 subunit gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 1624108 Ap3s2 adaptor-related protein complex 3, sigma 2 subunit gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1624108 Ap3s2 adaptor-related protein complex 3, sigma 2 subunit gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 1624108 Ap3s2 adaptor-related protein complex 3, sigma 2 subunit gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 1624108 Ap3s2 adaptor-related protein complex 3, sigma 2 subunit gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0002083 premature death IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0008012 duodenum polyps IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0008109 abnormal small intestinal microvillus morphology IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0011882 enlarged duodenum IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0013482 abnormal duodenum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0013483 abnormal jejunum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624109 Ap1m2 adaptor protein complex AP-1, mu 2 subunit gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20160728 MGI PMID:23684748 1624404 Fcrl6 Fc receptor-like 6 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20210128 MGI 1624440 Morrbid myeloid RNA regulator of BCL2L11 induced cell death gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20190919 MGI PMID:27525555 1624440 Morrbid myeloid RNA regulator of BCL2L11 induced cell death gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20190919 MGI PMID:27525555 1624440 Morrbid myeloid RNA regulator of BCL2L11 induced cell death gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20190919 MGI PMID:27525555 1624440 Morrbid myeloid RNA regulator of BCL2L11 induced cell death gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20190919 MGI PMID:27525555 1624440 Morrbid myeloid RNA regulator of BCL2L11 induced cell death gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20190919 MGI PMID:27525555 1624440 Morrbid myeloid RNA regulator of BCL2L11 induced cell death gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20190919 MGI PMID:27525555 1624440 Morrbid myeloid RNA regulator of BCL2L11 induced cell death gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20190919 MGI PMID:27525555 1624440 Morrbid myeloid RNA regulator of BCL2L11 induced cell death gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20190919 MGI PMID:27525555 1624440 Morrbid myeloid RNA regulator of BCL2L11 induced cell death gene MP:0013023 decreased Ly6C high monocyte number IAGP N RGD:5509061 20190919 MGI PMID:27525555 1624440 Morrbid myeloid RNA regulator of BCL2L11 induced cell death gene MP:0013026 decreased Ly6C low monocyte number IAGP N RGD:5509061 20190919 MGI PMID:27525555 1624448 Cep85l centrosomal protein 85-like gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 1624448 Cep85l centrosomal protein 85-like gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20231207 MGI 1624448 Cep85l centrosomal protein 85-like gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20210520 MGI 1624448 Cep85l centrosomal protein 85-like gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210520 MGI 1624448 Cep85l centrosomal protein 85-like gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 1624448 Cep85l centrosomal protein 85-like gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 1624448 Cep85l centrosomal protein 85-like gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 1624448 Cep85l centrosomal protein 85-like gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 1624448 Cep85l centrosomal protein 85-like gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 1624448 Cep85l centrosomal protein 85-like gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 1624448 Cep85l centrosomal protein 85-like gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 1624448 Cep85l centrosomal protein 85-like gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 1624474 Fam124a family with sequence similarity 124, member A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 1624474 Fam124a family with sequence similarity 124, member A gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 1624474 Fam124a family with sequence similarity 124, member A gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1624474 Fam124a family with sequence similarity 124, member A gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 1624474 Fam124a family with sequence similarity 124, member A gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 1624474 Fam124a family with sequence similarity 124, member A gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 1624474 Fam124a family with sequence similarity 124, member A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 1624618 Prcd photoreceptor disc component gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20191114 MGI PMID:31189593 1624618 Prcd photoreceptor disc component gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20191114 MGI PMID:31189593 1624618 Prcd photoreceptor disc component gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20191114 MGI PMID:31189593 1624618 Prcd photoreceptor disc component gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20191114 MGI PMID:31189593 1624618 Prcd photoreceptor disc component gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20191114 MGI PMID:31189593 1624618 Prcd photoreceptor disc component gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20191114 MGI PMID:31189593 1624618 Prcd photoreceptor disc component gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20191114 MGI PMID:31189593 1624618 Prcd photoreceptor disc component gene MP:0020814 abnormal photoreceptor outer segment diameter IAGP N RGD:5509061 20191114 MGI PMID:31189593 1624690 Cd101 CD101 antigen gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:21613616 1624719 Apela apelin receptor early endogenous ligand gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0001787 pericardial edema IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0001933 abnormal litter size IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230126 MGI PMID:29420831 1624719 Apela apelin receptor early endogenous ligand gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0003718 maternal effect IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0009658 increased placenta apoptosis IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0010662 abnormal intersomitic artery morphology IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0011433 glomerular capillary congestion IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0011455 absent glomerular endothelium fenestra IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0011531 abnormal syncytiotrophoblast morphology IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0014044 absent cardiac outflow tract IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624719 Apela apelin receptor early endogenous ligand gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180315 MGI PMID:28663440 1624739 Ppp1r36dn Ppp1r36 downstream neighbor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230126 MGI PMID:29420831 1624744 Gm15441 predicted gene 15441 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20210325 MGI PMID:33203882 1624744 Gm15441 predicted gene 15441 gene MP:0011578 increased lipoprotein lipase activity IAGP N RGD:5509061 20210325 MGI PMID:33203882 1624787 Spink13 serine peptidase inhibitor, Kazal type 13 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 1624787 Spink13 serine peptidase inhibitor, Kazal type 13 gene MP:0000274 enlarged heart IEA N RGD:5509061 20201022 MGI 1624787 Spink13 serine peptidase inhibitor, Kazal type 13 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 1624787 Spink13 serine peptidase inhibitor, Kazal type 13 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20201022 MGI 1624787 Spink13 serine peptidase inhibitor, Kazal type 13 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20201022 MGI 1624787 Spink13 serine peptidase inhibitor, Kazal type 13 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 1624787 Spink13 serine peptidase inhibitor, Kazal type 13 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 1624787 Spink13 serine peptidase inhibitor, Kazal type 13 gene MP:0003604 single kidney IEA N RGD:5509061 20210128 MGI 1624787 Spink13 serine peptidase inhibitor, Kazal type 13 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20221215 MGI 1624876 Spint3 serine peptidase inhibitor, Kunitz type, 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210506 MGI PMID:32814578 1624883 Gm13547 predicted gene 13547 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20201231 MGI 1624885 Mterf1b mitochondrial transcription termination factor 1b gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23562081 1624887 Rnaset2b ribonuclease T2B gene MP:0000691 enlarged spleen IEA N RGD:5509061 20170105 MGI 1624887 Rnaset2b ribonuclease T2B gene MP:0003068 enlarged kidney IEA N RGD:5509061 20170105 MGI 1624887 Rnaset2b ribonuclease T2B gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220811 MGI 1624887 Rnaset2b ribonuclease T2B gene MP:0010052 increased grip strength IEA N RGD:5509061 20160421 MGI 1624895 Dux double homeobox gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20201210 MGI PMID:31806660 1624895 Dux double homeobox gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20201210 MGI PMID:31806660 1624895 Dux double homeobox gene MP:0001935 decreased litter size IAGP N RGD:5509061 20201210 MGI PMID:31806660 1624895 Dux double homeobox gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20201210 MGI PMID:31806660 1624895 Dux double homeobox gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20201210 MGI PMID:31806660 1624895 Dux double homeobox gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20201210 MGI PMID:31806660 1624895 Dux double homeobox gene MP:0012008 delayed parturition IAGP N RGD:5509061 20201210 MGI PMID:31806660 1624895 Dux double homeobox gene MP:0012128 abnormal blastocyst formation IAGP N RGD:5509061 20201210 MGI PMID:31806660 1624947 Gm6812 predicted gene 6812 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201224 MGI PMID:32493902 1625156 Tomt transmembrane O-methyltransferase gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:18794526 1625156 Tomt transmembrane O-methyltransferase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18794526 1625156 Tomt transmembrane O-methyltransferase gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:18794526 1625156 Tomt transmembrane O-methyltransferase gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:18794526 1625156 Tomt transmembrane O-methyltransferase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:18794526 1625156 Tomt transmembrane O-methyltransferase gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:18794526 1625156 Tomt transmembrane O-methyltransferase gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:18794526 1625156 Tomt transmembrane O-methyltransferase gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:18794526 1625156 Tomt transmembrane O-methyltransferase gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18794526 1625156 Tomt transmembrane O-methyltransferase gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18794526 1625156 Tomt transmembrane O-methyltransferase gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:18794526 1625156 Tomt transmembrane O-methyltransferase gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:18794526 1625156 Tomt transmembrane O-methyltransferase gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:18794526 1625156 Tomt transmembrane O-methyltransferase gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18794526 1625156 Tomt transmembrane O-methyltransferase gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18794526 1625472 Pgls 6-phosphogluconolactonase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20160707 MGI PMID:26001274 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20160707 MGI PMID:26001274 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0000263 absent organized vascular network IAGP N RGD:5509061 20160211 MGI PMID:24958852 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20181227 MGI 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20160707 MGI PMID:26001274 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190808 MGI 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0001722 pale yolk sac IEA N RGD:5509061 20210520 MGI 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20160211 MGI PMID:24958852 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20170223 MGI PMID:25119035 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:24958852 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20160707 MGI PMID:26001274 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20160707 MGI PMID:26001274 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20170223 MGI PMID:25119035 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160211 MGI PMID:24958852 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20170223 MGI PMID:25119035 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20170223 MGI PMID:25119035 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20160211 MGI PMID:24958852 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20160707 MGI PMID:26001274 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20190808 MGI 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20160211 MGI PMID:24958852 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20160707 MGI PMID:26001274 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20170223 MGI PMID:25119035 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20160707 MGI PMID:26001274 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20190808 MGI 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20170223 MGI PMID:25119035 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20160707 MGI PMID:26001274 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0008998 decreased blood osmolality IAGP N RGD:5509061 20160707 MGI PMID:26001274 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20160211 MGI PMID:24958852 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20160707 MGI PMID:26001274 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20160211 MGI PMID:24958852 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20170223 MGI PMID:25119035 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20160211 MGI PMID:24958852 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20170223 MGI PMID:25119035 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20160211 MGI PMID:24958852 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0012384 abnormal erythrocyte ion transport IAGP N RGD:5509061 20160707 MGI PMID:26001274 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0012664 decreased circulating haptoglobin level IAGP N RGD:5509061 20160707 MGI PMID:26001274 1625473 Piezo1 piezo-type mechanosensitive ion channel component 1 gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:26001274 1625474 Myh7b myosin, heavy chain 7B, cardiac muscle, beta gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 1625474 Myh7b myosin, heavy chain 7B, cardiac muscle, beta gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 1625862 Mir216b microRNA 216b gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20191017 MGI PMID:31367007 1625862 Mir216b microRNA 216b gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20191017 MGI PMID:31367007 1625862 Mir216b microRNA 216b gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20191017 MGI PMID:31367007 1625867 Mir708 microRNA 708 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20220217 MGI PMID:34934045 1625867 Mir708 microRNA 708 gene MP:0002083 premature death IAGP N RGD:5509061 20220217 MGI PMID:34934045 1625867 Mir708 microRNA 708 gene MP:0014201 abnormal intestinal epithelium physiology IAGP N RGD:5509061 20220217 MGI PMID:34934045 1625875 Mir499 microRNA 499 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19922871 1625875 Mir499 microRNA 499 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:19922871 1625882 Mir592 microRNA 592 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0001260 increased body weight IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0012065 increased astrocyte number IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625882 Mir592 microRNA 592 gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20240627 MGI PMID:35365601 1625885 Mir455 microRNA 455 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20210506 MGI PMID:29748607 1625885 Mir455 microRNA 455 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20210506 MGI PMID:31508417 1625885 Mir455 microRNA 455 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20210506 MGI PMID:29748607 1625892 Mir181d microRNA 181d gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141106 MGI PMID:24416377 1625895 Mir743 microRNA 743 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201224 MGI PMID:32493902 1625897 Mageb5b MAGE family member B5B gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20230420 MGI PMID:35595785 1625897 Mageb5b MAGE family member B5B gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230420 MGI PMID:35595785 1625905 Rad21l RAD21-like (S. pombe) gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0001147 small testis IAGP N RGD:5509061 20150226 MGI PMID:24589552 1625905 Rad21l RAD21-like (S. pombe) gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0001925 male infertility IAGP N RGD:5509061 20150226 MGI PMID:24589552 1625905 Rad21l RAD21-like (S. pombe) gene MP:0001926 female infertility IAGP N RGD:5509061 20150226 MGI PMID:24589552 1625905 Rad21l RAD21-like (S. pombe) gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20150226 MGI PMID:24589552 1625905 Rad21l RAD21-like (S. pombe) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20150226 MGI PMID:24589552 1625905 Rad21l RAD21-like (S. pombe) gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20211021 MGI 1625905 Rad21l RAD21-like (S. pombe) gene MP:0004805 absent oocytes IAGP N RGD:5509061 20150226 MGI PMID:24589552 1625905 Rad21l RAD21-like (S. pombe) gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20150226 MGI PMID:24589552 1625905 Rad21l RAD21-like (S. pombe) gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20150226 MGI PMID:24589552 1625905 Rad21l RAD21-like (S. pombe) gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:24413433 1625905 Rad21l RAD21-like (S. pombe) gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20150226 MGI PMID:24589552 1625905 Rad21l RAD21-like (S. pombe) gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170105 MGI 1625905 Rad21l RAD21-like (S. pombe) gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20150226 MGI PMID:24589552 1625905 Rad21l RAD21-like (S. pombe) gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20150226 MGI PMID:24589552 1625905 Rad21l RAD21-like (S. pombe) gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20150226 MGI PMID:24589552 1625905 Rad21l RAD21-like (S. pombe) gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20210304 MGI PMID:30853435 1625905 Rad21l RAD21-like (S. pombe) gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20210304 MGI PMID:30853435 1625905 Rad21l RAD21-like (S. pombe) gene MP:0011122 absent primordial ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:21743440 1625905 Rad21l RAD21-like (S. pombe) gene MP:0013607 ovary fibrosis IAGP N RGD:5509061 20150312 MGI PMID:21743440 1625908 Tox2 TOX high mobility group box family member 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 1625908 Tox2 TOX high mobility group box family member 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 1625908 Tox2 TOX high mobility group box family member 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 1625908 Tox2 TOX high mobility group box family member 2 gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 1625908 Tox2 TOX high mobility group box family member 2 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20241031 MGI PMID:31732165 1625908 Tox2 TOX high mobility group box family member 2 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 1625908 Tox2 TOX high mobility group box family member 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 1625908 Tox2 TOX high mobility group box family member 2 gene MP:0010188 abnormal T follicular helper cell differentiation IAGP N RGD:5509061 20241031 MGI PMID:31732165 1625927 Nps neuropeptide S gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20231123 MGI PMID:28548278 1625927 Nps neuropeptide S gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20231123 MGI PMID:28548278 1625927 Nps neuropeptide S gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20231123 MGI PMID:28548278 1625929 Mir501 microRNA 501 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20240104 MGI PMID:35984881 1625929 Mir501 microRNA 501 gene MP:0012006 abnormal hippocampus physiology IAGP N RGD:5509061 20240104 MGI PMID:35984881 1625929 Mir501 microRNA 501 gene MP:0014256 decreased paired-pulse inhibition IAGP N RGD:5509061 20240104 MGI PMID:35984881 1625929 Mir501 microRNA 501 gene MP:0014378 increased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:35984881 1625929 Mir501 microRNA 501 gene MP:0020335 abnormal dentate gyrus neuron dendrite morphology IAGP N RGD:5509061 20240104 MGI PMID:35984881 1625929 Mir501 microRNA 501 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20240104 MGI PMID:35984881 1625929 Mir501 microRNA 501 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20240104 MGI PMID:35984881 1625929 Mir501 microRNA 501 gene MP:0021009 abnormal synaptic physiology IAGP N RGD:5509061 20240104 MGI PMID:35984881 1625929 Mir501 microRNA 501 gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20240104 MGI PMID:35984881 1625939 Mir146b microRNA 146b gene MP:0002493 increased IgG level IAGP N RGD:5509061 20190926 MGI PMID:30013024 1625939 Mir146b microRNA 146b gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20190926 MGI PMID:30013024 1625939 Mir146b microRNA 146b gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20190926 MGI PMID:30013024 1625940 Mir92-1 microRNA 92-1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20160211 MGI PMID:24979655 1625940 Mir92-1 microRNA 92-1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160211 MGI PMID:24979655 1625940 Mir92-1 microRNA 92-1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160211 MGI PMID:24979655 1625940 Mir92-1 microRNA 92-1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150924 MGI PMID:26029871 1625940 Mir92-1 microRNA 92-1 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20160211 MGI PMID:24979655 1625940 Mir92-1 microRNA 92-1 gene MP:0002764 short tibia IAGP N RGD:5509061 20160211 MGI PMID:24979655 1625940 Mir92-1 microRNA 92-1 gene MP:0005352 small cranium IAGP N RGD:5509061 20160211 MGI PMID:24979655 1625940 Mir92-1 microRNA 92-1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20160211 MGI PMID:24979655 1625940 Mir92-1 microRNA 92-1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160211 MGI PMID:24979655 1625944 Mir505 microRNA 505 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200813 MGI PMID:30557853 1625944 Mir505 microRNA 505 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200813 MGI PMID:30557853 1625944 Mir505 microRNA 505 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20200813 MGI PMID:30557853 1625944 Mir505 microRNA 505 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20200813 MGI PMID:30557853 1625944 Mir505 microRNA 505 gene MP:0001934 increased litter size IAGP N RGD:5509061 20200813 MGI PMID:30557853 1625944 Mir505 microRNA 505 gene MP:0002681 increased corpora lutea number IAGP N RGD:5509061 20200813 MGI PMID:30557853 1625944 Mir505 microRNA 505 gene MP:0002865 increased growth rate IAGP N RGD:5509061 20200813 MGI PMID:30557853 1625944 Mir505 microRNA 505 gene MP:0003378 early sexual maturation IAGP N RGD:5509061 20200813 MGI PMID:30557853 1625944 Mir505 microRNA 505 gene MP:0004514 dystocia IAGP N RGD:5509061 20200813 MGI PMID:30557853 1625944 Mir505 microRNA 505 gene MP:0004855 increased ovary weight IAGP N RGD:5509061 20200813 MGI PMID:30557853 1625944 Mir505 microRNA 505 gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20200813 MGI PMID:30557853 1625944 Mir505 microRNA 505 gene MP:0008994 early vaginal opening IAGP N RGD:5509061 20200813 MGI PMID:30557853 1625982 Mir802 microRNA 802 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20201015 MGI PMID:32286278 1625982 Mir802 microRNA 802 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20201015 MGI PMID:32286278 1625982 Mir802 microRNA 802 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20201015 MGI PMID:32286278 1625982 Mir802 microRNA 802 gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20201015 MGI PMID:32286278 1625982 Mir802 microRNA 802 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20201015 MGI PMID:32286278 1625982 Mir802 microRNA 802 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20201015 MGI PMID:32286278 1625993 Rnf212 ring finger protein 212 gene MP:0001925 male infertility IEA N RGD:5509061 20160225 MGI 1625993 Rnf212 ring finger protein 212 gene MP:0002208 abnormal germ cell morphology IEA N RGD:5509061 20160225 MGI 1625993 Rnf212 ring finger protein 212 gene MP:0004852 decreased testis weight IEA N RGD:5509061 20160225 MGI 1625993 Rnf212 ring finger protein 212 gene MP:0004910 decreased seminal vesicle weight IEA N RGD:5509061 20160225 MGI 1625993 Rnf212 ring finger protein 212 gene MP:0005159 azoospermia IEA N RGD:5509061 20160225 MGI 1625993 Rnf212 ring finger protein 212 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:22761591 1625993 Rnf212 ring finger protein 212 gene MP:0008261 arrest of male meiosis IEA N RGD:5509061 20160225 MGI 1626274 Higd1c HIG1 domain family, member 1C gene MP:0003438 abnormal carotid body physiology IAGP N RGD:5509061 20240229 MGI PMID:36255054 1626274 Higd1c HIG1 domain family, member 1C gene MP:0005385 cardiovascular system phenotype IAGP N RGD:5509061 20240229 MGI PMID:36255054 1626274 Higd1c HIG1 domain family, member 1C gene MP:0005576 decreased pulmonary ventilation IAGP N RGD:5509061 20240229 MGI PMID:36255054 1626274 Higd1c HIG1 domain family, member 1C gene MP:0020843 abnormal type I cell of carotid body physiology IAGP N RGD:5509061 20240229 MGI PMID:36255054 1626274 Higd1c HIG1 domain family, member 1C gene MP:0031252 abnormal physiological response to hypoxia IAGP N RGD:5509061 20240229 MGI PMID:36255054 1626389 Nt5dc3 5'-nucleotidase domain containing 3 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20240822 MGI 1642513 Cyp3a41b cytochrome P450, family 3, subfamily a, polypeptide 41B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 2289776 Tcrd T cell receptor delta chain gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:22341446 2289776 Tcrd T cell receptor delta chain gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22341446 2289776 Tcrd T cell receptor delta chain gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19017966 2289776 Tcrd T cell receptor delta chain gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:18203137 2289776 Tcrd T cell receptor delta chain gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:1359428 2289776 Tcrd T cell receptor delta chain gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:11927630 2289776 Tcrd T cell receptor delta chain gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:11927630 2289776 Tcrd T cell receptor delta chain gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11937563 2289776 Tcrd T cell receptor delta chain gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16272283 2289776 Tcrd T cell receptor delta chain gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15770700 2289776 Tcrd T cell receptor delta chain gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:1359428 2289776 Tcrd T cell receptor delta chain gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:1359428 2289776 Tcrd T cell receptor delta chain gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22341446 2289776 Tcrd T cell receptor delta chain gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16473278 2289776 Tcrd T cell receptor delta chain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22341446 2289776 Tcrd T cell receptor delta chain gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:16272283 2289776 Tcrd T cell receptor delta chain gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11937563 2289776 Tcrd T cell receptor delta chain gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:16272283 2289776 Tcrd T cell receptor delta chain gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12049722 2289776 Tcrd T cell receptor delta chain gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18203137 2289776 Tcrd T cell receptor delta chain gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16473278 2289776 Tcrd T cell receptor delta chain gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18203137 2289776 Tcrd T cell receptor delta chain gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12049722 2289776 Tcrd T cell receptor delta chain gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11937563 2289776 Tcrd T cell receptor delta chain gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15770700 2289776 Tcrd T cell receptor delta chain gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:16439970 2289776 Tcrd T cell receptor delta chain gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:8104709 2289776 Tcrd T cell receptor delta chain gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:12486099 2289776 Tcrd T cell receptor delta chain gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:1359428 2289776 Tcrd T cell receptor delta chain gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:19017966 2289776 Tcrd T cell receptor delta chain gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20231221 MGI PMID:36198790 2289776 Tcrd T cell receptor delta chain gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:12049722 2289776 Tcrd T cell receptor delta chain gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 2289776 Tcrd T cell receptor delta chain gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:15770700 2289776 Tcrd T cell receptor delta chain gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15770700 2289776 Tcrd T cell receptor delta chain gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:16272283 2289776 Tcrd T cell receptor delta chain gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:1359428 2289776 Tcrd T cell receptor delta chain gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18203137 2289776 Tcrd T cell receptor delta chain gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11927630 2289776 Tcrd T cell receptor delta chain gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15592472 2289776 Tcrd T cell receptor delta chain gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:19017966 2289776 Tcrd T cell receptor delta chain gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0008188 abnormal transitional stage B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0008348 absent gamma-delta T cells IAGP N RGD:5509061 20141003 MGI PMID:8381716 2289776 Tcrd T cell receptor delta chain gene MP:0008356 abnormal gamma-delta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8381716 2289776 Tcrd T cell receptor delta chain gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11937563 2289776 Tcrd T cell receptor delta chain gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20231221 MGI PMID:36198790 2289776 Tcrd T cell receptor delta chain gene MP:0008757 abnormal T cell receptor gamma chain V-J recombination IAGP N RGD:5509061 20141003 MGI PMID:11911829 2289776 Tcrd T cell receptor delta chain gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20231221 MGI PMID:36198790 2289776 Tcrd T cell receptor delta chain gene MP:0009925 increased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0010229 increased transitional stage T3 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22341446 2289776 Tcrd T cell receptor delta chain gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:22585710 2289776 Tcrd T cell receptor delta chain gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20231221 MGI PMID:36198790 2289776 Tcrd T cell receptor delta chain gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20231221 MGI PMID:36198790 2289776 Tcrd T cell receptor delta chain gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20231221 MGI PMID:36198790 2289776 Tcrd T cell receptor delta chain gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:22585710 2289889 Gm14496 predicted gene 14496 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20181227 MGI 2289889 Gm14496 predicted gene 14496 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 2289889 Gm14496 predicted gene 14496 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20181227 MGI 2289889 Gm14496 predicted gene 14496 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20181227 MGI 2289889 Gm14496 predicted gene 14496 gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 2290037 Trabd2b TraB domain containing 2B gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20200514 MGI 2290037 Trabd2b TraB domain containing 2B gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20200514 MGI 2290037 Trabd2b TraB domain containing 2B gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20200514 MGI 2290037 Trabd2b TraB domain containing 2B gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20200514 MGI 2290037 Trabd2b TraB domain containing 2B gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20200514 MGI 2290037 Trabd2b TraB domain containing 2B gene MP:0000642 enlarged adrenal glands IEA N RGD:5509061 20200514 MGI 2290037 Trabd2b TraB domain containing 2B gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20200514 MGI 2290037 Trabd2b TraB domain containing 2B gene MP:0000709 enlarged thymus IEA N RGD:5509061 20200514 MGI 2290037 Trabd2b TraB domain containing 2B gene MP:0001891 hydrocephaly IEA N RGD:5509061 20200514 MGI 2290037 Trabd2b TraB domain containing 2B gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20200514 MGI 2290037 Trabd2b TraB domain containing 2B gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20201231 MGI 2290037 Trabd2b TraB domain containing 2B gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20211021 MGI 2290037 Trabd2b TraB domain containing 2B gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20200514 MGI 2290037 Trabd2b TraB domain containing 2B gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 2290320 Snhg14 small nucleolar RNA host gene 14 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141030 MGI PMID:24385930 2290320 Snhg14 small nucleolar RNA host gene 14 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141030 MGI PMID:24385930 2290320 Snhg14 small nucleolar RNA host gene 14 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141030 MGI PMID:24385930 2290334 Xaf1 XIAP associated factor 1 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210520 MGI 2290334 Xaf1 XIAP associated factor 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 2290334 Xaf1 XIAP associated factor 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20240620 MGI PMID:37384528 2290334 Xaf1 XIAP associated factor 1 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20220811 MGI 2290334 Xaf1 XIAP associated factor 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20240620 MGI PMID:37384528 2290334 Xaf1 XIAP associated factor 1 gene MP:0003883 enlarged stomach IEA N RGD:5509061 20210520 MGI 2290334 Xaf1 XIAP associated factor 1 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20240620 MGI PMID:37384528 2290334 Xaf1 XIAP associated factor 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20240620 MGI PMID:37384528 2290334 Xaf1 XIAP associated factor 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240620 MGI PMID:37384528 2290334 Xaf1 XIAP associated factor 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20240620 MGI PMID:37384528 2290334 Xaf1 XIAP associated factor 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20240620 MGI PMID:37384528 2290337 Fancf Fanconi anemia, complementation group F gene MP:0001127 small ovary IAGP N RGD:5509061 20180111 MGI PMID:21915857 2290337 Fancf Fanconi anemia, complementation group F gene MP:0001314 cornea opacity IEA N RGD:5509061 20220811 MGI 2290337 Fancf Fanconi anemia, complementation group F gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20180111 MGI PMID:21915857 2290337 Fancf Fanconi anemia, complementation group F gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20180111 MGI PMID:21915857 2290337 Fancf Fanconi anemia, complementation group F gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20180111 MGI PMID:21915857 2290337 Fancf Fanconi anemia, complementation group F gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20180111 MGI PMID:21915857 2290337 Fancf Fanconi anemia, complementation group F gene MP:0002083 premature death IAGP N RGD:5509061 20180111 MGI PMID:21915857 2290337 Fancf Fanconi anemia, complementation group F gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 2290337 Fancf Fanconi anemia, complementation group F gene MP:0004025 polyploidy IAGP N RGD:5509061 20180111 MGI PMID:21915857 2290337 Fancf Fanconi anemia, complementation group F gene MP:0005159 azoospermia IAGP N RGD:5509061 20180111 MGI PMID:21915857 2290337 Fancf Fanconi anemia, complementation group F gene MP:0005542 cornea vascularization IEA N RGD:5509061 20240523 MGI 2290337 Fancf Fanconi anemia, complementation group F gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20180111 MGI PMID:21915857 2290337 Fancf Fanconi anemia, complementation group F gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20180111 MGI PMID:21915857 2290337 Fancf Fanconi anemia, complementation group F gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20180111 MGI PMID:21915857 2290337 Fancf Fanconi anemia, complementation group F gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180111 MGI PMID:21915857 2290337 Fancf Fanconi anemia, complementation group F gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20180111 MGI PMID:21915857 2290337 Fancf Fanconi anemia, complementation group F gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20180111 MGI PMID:21915857 2290337 Fancf Fanconi anemia, complementation group F gene MP:0012121 sclerocornea IEA N RGD:5509061 20240523 MGI 2290337 Fancf Fanconi anemia, complementation group F gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20180111 MGI PMID:21915857 2290341 Pantr1 POU domain, class 3, transcription factor 3 adjacent noncoding transcript 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24381249 2290525 Dlx6os1 distal-less homeobox 6, opposite strand 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19620975 2290525 Dlx6os1 distal-less homeobox 6, opposite strand 1 gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20141003 MGI PMID:19620975 2290525 Dlx6os1 distal-less homeobox 6, opposite strand 1 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:19620975 2291825 Malat1 metastasis associated lung adenocarcinoma transcript 1 (non-coding RNA) gene MP:0001847 brain inflammation IAGP N RGD:5509061 20170525 MGI PMID:28093478 2291825 Malat1 metastasis associated lung adenocarcinoma transcript 1 (non-coding RNA) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22840402 2291825 Malat1 metastasis associated lung adenocarcinoma transcript 1 (non-coding RNA) gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20170525 MGI PMID:28093478 2291825 Malat1 metastasis associated lung adenocarcinoma transcript 1 (non-coding RNA) gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20170525 MGI PMID:28093478 2291825 Malat1 metastasis associated lung adenocarcinoma transcript 1 (non-coding RNA) gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20170525 MGI PMID:28093478 2291825 Malat1 metastasis associated lung adenocarcinoma transcript 1 (non-coding RNA) gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20170525 MGI PMID:28093478 2291953 Nlgn4l neuroligin 4-like gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:18227507 2291953 Nlgn4l neuroligin 4-like gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:18227507 2291953 Nlgn4l neuroligin 4-like gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:18227507 2291953 Nlgn4l neuroligin 4-like gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:18227507 2291954 Nct2 non-coding in testis 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18401007 2291955 Nct1 non-coding in testis 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18401007 2292250 Pnp2 purine-nucleoside phosphorylase 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20240926 MGI PMID:31675497 2292361 Mir9-2hg Mir9-2 host gene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160317 MGI PMID:25209608 2292378 Tmem35b transmembrane protein 35B gene MP:0001513 limb grasping IEA N RGD:5509061 20230601 MGI 2292393 E130114P18Rik RIKEN cDNA E130114P18 gene gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 2292393 E130114P18Rik RIKEN cDNA E130114P18 gene gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 2292393 E130114P18Rik RIKEN cDNA E130114P18 gene gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 2292400 Mtln mitoregulin gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20180809 MGI PMID:29949756 2292400 Mtln mitoregulin gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20180809 MGI PMID:29949756 2292400 Mtln mitoregulin gene MP:0014174 decreased fatty acid beta-oxidation IAGP N RGD:5509061 20180809 MGI PMID:29949756 2293036 Stmp1 short transmembrane mitochondrial protein 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20220811 MGI PMID:35101990 2293036 Stmp1 short transmembrane mitochondrial protein 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20220811 MGI PMID:35101990 2293945 Gm13570 predicted gene 13570 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240627 MGI PMID:38835510 2293981 R3hdml R3H domain containing-like gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20200130 MGI PMID:31524320 2293981 R3hdml R3H domain containing-like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200130 MGI PMID:31524320 2293981 R3hdml R3H domain containing-like gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200130 MGI PMID:31524320 2293981 R3hdml R3H domain containing-like gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20200130 MGI PMID:31524320 2293981 R3hdml R3H domain containing-like gene MP:0004093 diffuse Z line IAGP N RGD:5509061 20200130 MGI PMID:31524320 2293981 R3hdml R3H domain containing-like gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20200130 MGI PMID:31524320 2293981 R3hdml R3H domain containing-like gene MP:0009410 abnormal skeletal muscle satellite cell proliferation IAGP N RGD:5509061 20200130 MGI PMID:31524320 2293981 R3hdml R3H domain containing-like gene MP:0010225 abnormal quadriceps morphology IAGP N RGD:5509061 20200130 MGI PMID:31524320 2293981 R3hdml R3H domain containing-like gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20200130 MGI PMID:31524320 2293981 R3hdml R3H domain containing-like gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20200130 MGI PMID:31524320 2294075 Zfp831 zinc finger protein 831 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20190502 MGI 2294075 Zfp831 zinc finger protein 831 gene MP:0002764 short tibia IEA N RGD:5509061 20220519 MGI 2294075 Zfp831 zinc finger protein 831 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20191128 MGI 2294131 Ccdc8 coiled-coil domain containing 8 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20210617 MGI PMID:31343991 2294131 Ccdc8 coiled-coil domain containing 8 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20210617 MGI PMID:31343991 2294131 Ccdc8 coiled-coil domain containing 8 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20210617 MGI PMID:31343991 2294131 Ccdc8 coiled-coil domain containing 8 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20210617 MGI PMID:31343991 2294131 Ccdc8 coiled-coil domain containing 8 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 2294131 Ccdc8 coiled-coil domain containing 8 gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20210617 MGI PMID:31343991 2294131 Ccdc8 coiled-coil domain containing 8 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20210617 MGI PMID:31343991 2294131 Ccdc8 coiled-coil domain containing 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200310 MGI 2294131 Ccdc8 coiled-coil domain containing 8 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20210617 MGI PMID:31343991 2294131 Ccdc8 coiled-coil domain containing 8 gene MP:0011525 abnormal placenta intervillous maternal lacunae morphology IAGP N RGD:5509061 20210617 MGI PMID:31343991 2294131 Ccdc8 coiled-coil domain containing 8 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20210617 MGI PMID:31343991 2294157 Snhg15 small nucleolar RNA host gene 15 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20201224 MGI PMID:32483152 2294157 Snhg15 small nucleolar RNA host gene 15 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20201224 MGI PMID:32483152 2294157 Snhg15 small nucleolar RNA host gene 15 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20201224 MGI PMID:32483152 2294157 Snhg15 small nucleolar RNA host gene 15 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211104 MGI PMID:32483152 2294157 Snhg15 small nucleolar RNA host gene 15 gene MP:0031328 delayed skeletal muscle regeneration IAGP N RGD:5509061 20220106 MGI PMID:32483152 2294204 Ldlrad1 low density lipoprotein receptor class A domain containing 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20200514 MGI 2294213 Obp2b odorant binding protein 2B gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 2294213 Obp2b odorant binding protein 2B gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20240523 MGI 2294213 Obp2b odorant binding protein 2B gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 2294213 Obp2b odorant binding protein 2B gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20240523 MGI 2294213 Obp2b odorant binding protein 2B gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230601 MGI 2294213 Obp2b odorant binding protein 2B gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20240523 MGI 2294213 Obp2b odorant binding protein 2B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 2294384 Tigit T cell immunoreceptor with Ig and ITIM domains gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20221027 MGI 2294384 Tigit T cell immunoreceptor with Ig and ITIM domains gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21199897 2294384 Tigit T cell immunoreceptor with Ig and ITIM domains gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21199897 2294384 Tigit T cell immunoreceptor with Ig and ITIM domains gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21199897 2294384 Tigit T cell immunoreceptor with Ig and ITIM domains gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20221027 MGI 2294384 Tigit T cell immunoreceptor with Ig and ITIM domains gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21199897 2294821 Skint1 selection and upkeep of intraepithelial T cells 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141106 MGI PMID:18408721 2294821 Skint1 selection and upkeep of intraepithelial T cells 1 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141106 MGI PMID:18408721 2295020 Susd1 sushi domain containing 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 2295020 Susd1 sushi domain containing 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 2295020 Susd1 sushi domain containing 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 2295020 Susd1 sushi domain containing 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20201022 MGI 2295120 Lrrc55os leucine rich repeat containing 55, opposite strand gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20201217 MGI PMID:31213650 2295120 Lrrc55os leucine rich repeat containing 55, opposite strand gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20201217 MGI PMID:31213650 2295120 Lrrc55os leucine rich repeat containing 55, opposite strand gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20201231 MGI PMID:31213650 2295243 H3f4 H3.4 histone, cluster member gene MP:0001147 small testis IAGP N RGD:5509061 20191003 MGI PMID:28099840 2295243 H3f4 H3.4 histone, cluster member gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20191003 MGI PMID:28099840 2295243 H3f4 H3.4 histone, cluster member gene MP:0001925 male infertility IAGP N RGD:5509061 20191003 MGI PMID:28099840 2295243 H3f4 H3.4 histone, cluster member gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20191003 MGI PMID:28099840 2295243 H3f4 H3.4 histone, cluster member gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20191003 MGI PMID:28099840 2295243 H3f4 H3.4 histone, cluster member gene MP:0005159 azoospermia IAGP N RGD:5509061 20191003 MGI PMID:28099840 2295243 H3f4 H3.4 histone, cluster member gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20191003 MGI PMID:28099840 2295243 H3f4 H3.4 histone, cluster member gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20191003 MGI PMID:28099840 2295243 H3f4 H3.4 histone, cluster member gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20191003 MGI PMID:28099840 2295243 H3f4 H3.4 histone, cluster member gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20191003 MGI PMID:28099840 2295243 H3f4 H3.4 histone, cluster member gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20191003 MGI PMID:28099840 2295316 Spocd1 SPOC domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20201105 MGI PMID:32674113 2295316 Spocd1 SPOC domain containing 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20201105 MGI PMID:32674113 2295316 Spocd1 SPOC domain containing 1 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20201105 MGI PMID:32674113 2295316 Spocd1 SPOC domain containing 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20201105 MGI PMID:32674113 2295316 Spocd1 SPOC domain containing 1 gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20201105 MGI PMID:32674113 2295316 Spocd1 SPOC domain containing 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20201105 MGI PMID:32674113 2295316 Spocd1 SPOC domain containing 1 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20201105 MGI PMID:32674113 2295316 Spocd1 SPOC domain containing 1 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20201105 MGI PMID:32674113 2295330 Krtap9-5 keratin associated protein 9-5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 2295330 Krtap9-5 keratin associated protein 9-5 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220519 MGI 2295330 Krtap9-5 keratin associated protein 9-5 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220519 MGI 2295330 Krtap9-5 keratin associated protein 9-5 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20220519 MGI 2295330 Krtap9-5 keratin associated protein 9-5 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 2295330 Krtap9-5 keratin associated protein 9-5 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20220811 MGI 2295330 Krtap9-5 keratin associated protein 9-5 gene MP:0013129 abnormal tooth color IEA N RGD:5509061 20220519 MGI 2295493 Arhgap40 Rho GTPase activating protein 40 gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20240523 MGI 2295612 Msmp microseminoprotein, prostate associated gene MP:0001860 liver inflammation IAGP N RGD:5509061 20211021 MGI PMID:31813573 2295612 Msmp microseminoprotein, prostate associated gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20211021 MGI PMID:31813573 2295612 Msmp microseminoprotein, prostate associated gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20211021 MGI PMID:31813573 2295612 Msmp microseminoprotein, prostate associated gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20211021 MGI PMID:31813573 2295612 Msmp microseminoprotein, prostate associated gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20211021 MGI PMID:31813573 2295612 Msmp microseminoprotein, prostate associated gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20211021 MGI PMID:31813573 2295612 Msmp microseminoprotein, prostate associated gene MP:0008838 decreased transforming growth factor beta level IAGP N RGD:5509061 20211021 MGI PMID:31813573 2295612 Msmp microseminoprotein, prostate associated gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20211021 MGI PMID:31813573 2295870 H2ab1 H2A.B variant histone 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20190627 MGI PMID:30704500 2295870 H2ab1 H2A.B variant histone 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20190627 MGI PMID:30704500 2295870 H2ab1 H2A.B variant histone 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20190627 MGI PMID:30704500 2295870 H2ab1 H2A.B variant histone 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20190627 MGI PMID:30704500 2295870 H2ab1 H2A.B variant histone 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20190627 MGI PMID:30704500 2295870 H2ab1 H2A.B variant histone 1 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20190627 MGI PMID:30704500 2295870 H2ab1 H2A.B variant histone 1 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20190627 MGI PMID:30704500 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20150108 MGI 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20181227 MGI 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0003962 abnormal adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20150108 MGI 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0011958 increased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:23869016 2295926 Mrap2 melanocortin 2 receptor accessory protein 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 2299015 Klrb1 killer cell lectin-like receptor subfamily B member 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 2299015 Klrb1 killer cell lectin-like receptor subfamily B member 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 2299015 Klrb1 killer cell lectin-like receptor subfamily B member 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 2299015 Klrb1 killer cell lectin-like receptor subfamily B member 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 2299015 Klrb1 killer cell lectin-like receptor subfamily B member 1 gene MP:0008173 increased follicular B cell number IEA N RGD:5509061 20210826 MGI 2299015 Klrb1 killer cell lectin-like receptor subfamily B member 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210128 MGI 2299015 Klrb1 killer cell lectin-like receptor subfamily B member 1 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20210128 MGI 2299015 Klrb1 killer cell lectin-like receptor subfamily B member 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20181227 MGI 2299015 Klrb1 killer cell lectin-like receptor subfamily B member 1 gene MP:0010574 dilated aorta IEA N RGD:5509061 20181227 MGI 2299306 Mfsd4b4 major facilitator superfamily domain containing 4B4 gene MP:0001513 limb grasping IEA N RGD:5509061 20210520 MGI 2299306 Mfsd4b4 major facilitator superfamily domain containing 4B4 gene MP:0001523 impaired righting response IEA N RGD:5509061 20210520 MGI 2299306 Mfsd4b4 major facilitator superfamily domain containing 4B4 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 2299475 Gm12695 predicted gene 12695 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0000111 cleft palate IEA N RGD:5509061 20210520 MGI 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20160825 MGI PMID:26402555 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20160825 MGI PMID:26402555 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0001435 absent suckling reflex IAGP N RGD:5509061 20160825 MGI PMID:26402555 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20160825 MGI PMID:26402555 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20160825 MGI PMID:26402555 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20160825 MGI PMID:26402555 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20160825 MGI PMID:26402555 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20160825 MGI PMID:26402555 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20160825 MGI PMID:26402555 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0010827 small lung saccule IAGP N RGD:5509061 20160825 MGI PMID:26402555 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160825 MGI PMID:26402555 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 2299525 Kcnj13 potassium inwardly-rectifying channel, subfamily J, member 13 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20190502 MGI 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24381249 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20221208 MGI PMID:33059001 2299758 Lncenc1 long non-coding RNA, embryonic stem cells expressed 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20221208 MGI PMID:33059001 2300037 Plscr5 phospholipid scramblase family, member 5 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220519 MGI 2300037 Plscr5 phospholipid scramblase family, member 5 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 2300037 Plscr5 phospholipid scramblase family, member 5 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 2301612 Gm14692 predicted gene 14692 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201224 MGI PMID:32493902 2301662 Ak9 adenylate kinase 9 gene MP:0001525 impaired balance IAGP N RGD:5509061 20240314 MGI PMID:38100419 2301662 Ak9 adenylate kinase 9 gene MP:0001924 infertility IAGP N RGD:5509061 20240314 MGI PMID:38100419 2301662 Ak9 adenylate kinase 9 gene MP:0001925 male infertility IAGP N RGD:5509061 20231102 MGI PMID:37713809 2301662 Ak9 adenylate kinase 9 gene MP:0001925 male infertility IAGP N RGD:5509061 20240314 MGI PMID:38100419 2301662 Ak9 adenylate kinase 9 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20240314 MGI PMID:38100419 2301662 Ak9 adenylate kinase 9 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20240314 MGI PMID:38100419 2301662 Ak9 adenylate kinase 9 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20231102 MGI PMID:37713809 2301662 Ak9 adenylate kinase 9 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20240314 MGI PMID:38100419 2301662 Ak9 adenylate kinase 9 gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20240314 MGI PMID:38100419 2301662 Ak9 adenylate kinase 9 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20240314 MGI PMID:38100419 2301662 Ak9 adenylate kinase 9 gene MP:0030964 decreased brain ependyma motile cilium length IAGP N RGD:5509061 20240314 MGI PMID:38100419 2301782 Isg15 ISG15 ubiquitin-like modifier gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20200310 MGI PMID:21402791 2301782 Isg15 ISG15 ubiquitin-like modifier gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20200310 MGI PMID:21402791 2301782 Isg15 ISG15 ubiquitin-like modifier gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20200310 MGI PMID:21402791 2301782 Isg15 ISG15 ubiquitin-like modifier gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20200310 MGI PMID:21402791 2301782 Isg15 ISG15 ubiquitin-like modifier gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20200310 MGI PMID:21402791 2302344 Sco2 SCO2 cytochrome c oxidase assembly protein gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:19837698 2302344 Sco2 SCO2 cytochrome c oxidase assembly protein gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:21723506 2302344 Sco2 SCO2 cytochrome c oxidase assembly protein gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20160331 MGI PMID:19837698 2302344 Sco2 SCO2 cytochrome c oxidase assembly protein gene MP:0003066 increased liver copper level IAGP N RGD:5509061 20141003 MGI PMID:19837698 2302344 Sco2 SCO2 cytochrome c oxidase assembly protein gene MP:0003952 abnormal copper level IAGP N RGD:5509061 20141003 MGI PMID:19837698 2302344 Sco2 SCO2 cytochrome c oxidase assembly protein gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:19837698 2302344 Sco2 SCO2 cytochrome c oxidase assembly protein gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19837698 2302344 Sco2 SCO2 cytochrome c oxidase assembly protein gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:19837698 2302512 Gm14725 predicted gene 14725 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230420 MGI PMID:35595785 2302587 Frrs1l ferric-chelate reductase 1 like gene MP:0001284 absent vibrissae IEA N RGD:5509061 20200402 MGI 2302587 Frrs1l ferric-chelate reductase 1 like gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 2302587 Frrs1l ferric-chelate reductase 1 like gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 2302587 Frrs1l ferric-chelate reductase 1 like gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 2302587 Frrs1l ferric-chelate reductase 1 like gene MP:0001512 trunk curl IEA N RGD:5509061 20160421 MGI 2302587 Frrs1l ferric-chelate reductase 1 like gene MP:0001513 limb grasping IEA N RGD:5509061 20160421 MGI 2302587 Frrs1l ferric-chelate reductase 1 like gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 2302587 Frrs1l ferric-chelate reductase 1 like gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160421 MGI 2302587 Frrs1l ferric-chelate reductase 1 like gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 2302590 Bcl2l15 BCLl2-like 15 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 2302590 Bcl2l15 BCLl2-like 15 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20181227 MGI 2302590 Bcl2l15 BCLl2-like 15 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 2302590 Bcl2l15 BCLl2-like 15 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210826 MGI 2302590 Bcl2l15 BCLl2-like 15 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 2302590 Bcl2l15 BCLl2-like 15 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 2302590 Bcl2l15 BCLl2-like 15 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 2302590 Bcl2l15 BCLl2-like 15 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 2302590 Bcl2l15 BCLl2-like 15 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 2302732 Ccl27b C-C motif chemokine ligand 27b gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20240613 MGI PMID:35663027 2302732 Ccl27b C-C motif chemokine ligand 27b gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20240613 MGI PMID:35663027 2302732 Ccl27b C-C motif chemokine ligand 27b gene MP:0009080 uterus inflammation IAGP N RGD:5509061 20240613 MGI PMID:35663027 2302732 Ccl27b C-C motif chemokine ligand 27b gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20240613 MGI PMID:35663027 2302732 Ccl27b C-C motif chemokine ligand 27b gene MP:0012572 increased susceptibility to chemically induced skin inflammation IAGP N RGD:5509061 20240613 MGI PMID:35663027 2302732 Ccl27b C-C motif chemokine ligand 27b gene MP:0020212 impaired leukocyte migration IAGP N RGD:5509061 20240613 MGI PMID:35663027 2302840 Ggct gamma-glutamyl cyclotransferase gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20220428 MGI PMID:34409610 2302840 Ggct gamma-glutamyl cyclotransferase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20220428 MGI PMID:34409610 2302840 Ggct gamma-glutamyl cyclotransferase gene MP:0001577 anemia IAGP N RGD:5509061 20220428 MGI PMID:34409610 2302840 Ggct gamma-glutamyl cyclotransferase gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20220428 MGI PMID:31400748 2302840 Ggct gamma-glutamyl cyclotransferase gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20220428 MGI PMID:34409610 2302840 Ggct gamma-glutamyl cyclotransferase gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20220428 MGI PMID:34409610 2302840 Ggct gamma-glutamyl cyclotransferase gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20220428 MGI PMID:34409610 2302840 Ggct gamma-glutamyl cyclotransferase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20220428 MGI PMID:34409610 2302840 Ggct gamma-glutamyl cyclotransferase gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20220428 MGI PMID:34409610 2302840 Ggct gamma-glutamyl cyclotransferase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220428 MGI PMID:34409610 2302840 Ggct gamma-glutamyl cyclotransferase gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20220428 MGI PMID:31400748 2302840 Ggct gamma-glutamyl cyclotransferase gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20220428 MGI PMID:34409610 2302840 Ggct gamma-glutamyl cyclotransferase gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20220428 MGI PMID:31400748 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22883231 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000015 abnormal ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:20880997 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000019 thick ears IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20170921 MGI PMID:17523175 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20171221 MGI PMID:28899994 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:21375737 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18832070 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:22155527 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20170427 MGI PMID:20499347 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000071 axial skeleton hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:22190459 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000088 short mandible IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000088 short mandible IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000088 short mandible IAGP N RGD:5509061 20221020 MGI PMID:32692983 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000088 short mandible IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17523175 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000111 cleft palate IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000114 cleft chin IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20210506 MGI PMID:33552067 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20170427 MGI PMID:20499347 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:18331721 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:18331721 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000154 rib fusion IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000160 kyphosis IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000160 kyphosis IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000161 scoliosis IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:19906844 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:19906844 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:22155527 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20180517 MGI PMID:29180569 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16951689 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20170921 MGI PMID:26668357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20210304 MGI PMID:30646909 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:17992256 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:21962509 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20191128 MGI PMID:23257357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:17875932 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19075395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19805914 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20959632 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:23455710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20170314 MGI PMID:25952549 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20210617 MGI PMID:33753942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20221215 MGI PMID:35973480 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17875932 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18056838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20230750 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21093323 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20161124 MGI PMID:26304963 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20190131 MGI PMID:28846072 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21724990 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20201022 MGI PMID:32343482 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20190131 MGI PMID:28846072 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16951689 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20230750 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20170314 MGI PMID:25952549 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23918954 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20170314 MGI PMID:25952549 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20170601 MGI PMID:26544067 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:23435463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18056838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24121508 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20151217 MGI PMID:24440599 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:19941827 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20959632 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:23455710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20150625 MGI PMID:25552701 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:17195237 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:21505259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20171109 MGI PMID:26774483 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20241107 MGI PMID:35477278 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:23178125 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18029401 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20170216 MGI PMID:26935106 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16720880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:21185281 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:24805242 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20191010 MGI PMID:30789911 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:21555590 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:22975327 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:19805914 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000274 enlarged heart IAGP N RGD:5509061 20160929 MGI PMID:25787764 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170810 MGI PMID:26356605 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000274 enlarged heart IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21068380 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20160929 MGI PMID:25787764 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170216 MGI PMID:26935106 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18297725 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20210121 MGI PMID:33127760 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231102 MGI PMID:35899771 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:23095891 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:19415626 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:18354198 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:19351831 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19075395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20161124 MGI PMID:26304963 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:16951689 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20170314 MGI PMID:25952549 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20170601 MGI PMID:26544067 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20150219 MGI PMID:24899231 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20160929 MGI PMID:25787764 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15048812 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16782029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17980593 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19061836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21376238 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22902753 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23209296 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20180315 MGI PMID:28481227 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19075002 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21191184 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20171207 MGI PMID:26847029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20160512 MGI PMID:25770585 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:21498671 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000371 diluted coat color IAGP N RGD:5509061 20150625 MGI PMID:25552701 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000371 diluted coat color IAGP N RGD:5509061 20181206 MGI PMID:29584722 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000373 belly spot IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20407033 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20181004 MGI PMID:27907123 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20190110 MGI PMID:27134165 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20141003 MGI PMID:20412777 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20141003 MGI PMID:20412777 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000405 abnormal auchene hair morphology IAGP N RGD:5509061 20141003 MGI PMID:20412777 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000412 excessive hair IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000413 polyphalangy IAGP N RGD:5509061 20141003 MGI PMID:19386268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000413 polyphalangy IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16885339 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:23293291 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000414 alopecia IAGP N RGD:5509061 20170126 MGI PMID:27435297 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000414 alopecia IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:17195237 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:23243018 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000423 delayed hair regrowth IAGP N RGD:5509061 20141003 MGI PMID:20412777 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000424 retarded hair growth IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23410975 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000440 domed cranium IAGP N RGD:5509061 20180517 MGI PMID:29180569 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:15699348 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:19047372 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000445 short snout IAGP N RGD:5509061 20180517 MGI PMID:29180569 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000445 short snout IAGP N RGD:5509061 20221020 MGI PMID:32692983 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:23893969 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20151022 MGI PMID:26324903 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21068065 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20180315 MGI PMID:28481227 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21703447 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21672919 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20150212 MGI PMID:24532689 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20025862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:24091011 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17980593 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18372904 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22354172 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23222438 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22354172 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22469981 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:23222438 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20150219 MGI PMID:24557836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:20404087 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20150625 MGI PMID:24732380 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20160714 MGI PMID:25194568 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:20040494 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:24656820 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000520 absent kidney IAGP N RGD:5509061 20220331 MGI PMID:30367465 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:16054034 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:20040494 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:20299358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:24656820 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20150625 MGI PMID:24732380 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17646578 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:18832070 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:19906844 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000547 short limbs IAGP N RGD:5509061 20180517 MGI PMID:29180569 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000551 absent forelimb IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:18423204 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:16221970 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:18832070 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19386268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000562 polydactyly IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000562 polydactyly IAGP N RGD:5509061 20151112 MGI PMID:23358455 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000564 syndactyly IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:24415953 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:22719891 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:17164415 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20141003 MGI PMID:20215352 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:23671110 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000585 kinked tail IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000585 kinked tail IAGP N RGD:5509061 20170427 MGI PMID:20499347 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:20230750 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18056838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:19234449 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:19551907 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141016 MGI PMID:24411941 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20151224 MGI PMID:24498102 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20191128 MGI PMID:23257357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:17875932 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:18056838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000599 enlarged liver IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000599 enlarged liver IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20230750 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:17646578 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:19551907 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:23712803 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21266350 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20201022 MGI PMID:31194862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000635 pituitary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16015321 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000649 sebaceous gland atrophy IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000653 abnormal sex gland morphology IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18043744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:22505453 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:21266350 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:23230003 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:16906226 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:18354198 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:20439541 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20170525 MGI PMID:26061883 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20170921 MGI PMID:26668357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17875932 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18056838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18663224 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20439541 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21093323 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23435463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23619366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141016 MGI PMID:23703832 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20150219 MGI PMID:24241423 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20151217 MGI PMID:24440599 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170921 MGI PMID:26668357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000692 small spleen IAGP N RGD:5509061 20170525 MGI PMID:26061883 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23619366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20170921 MGI PMID:26668357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:18663224 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:20363774 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20170525 MGI PMID:26061883 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15784609 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18663224 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20170921 MGI PMID:26668357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141120 MGI PMID:25053428 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000705 athymia IAGP N RGD:5509061 20150129 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:22770884 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000706 small thymus IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141120 MGI PMID:25053428 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:18331721 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:19554048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:17418413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15314171 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16791847 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:18641296 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19679071 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000745 tremors IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000745 tremors IAGP N RGD:5509061 20190829 MGI PMID:30520996 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:17418413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:20595581 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000747 muscle weakness IAGP N RGD:5509061 20190314 MGI PMID:30429376 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:19554048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:21828091 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:17418413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:23410975 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000751 myopathy IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:24132234 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17418413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21376238 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18329011 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15314171 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18202285 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21238928 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22017987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:21238928 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22017987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20180329 MGI PMID:29033352 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22017987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20230413 MGI PMID:35379703 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141218 MGI PMID:24501354 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20151224 MGI PMID:23696872 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:18509025 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:19279136 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:19357274 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:23444360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17537797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:19965762 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:22190459 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:23100420 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20818386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:17537797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000868 decreased anterior vermis size IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000869 abnormal cerebellum posterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18691547 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19965762 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23100420 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:19965762 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000874 irregular external granule cell layer thickness IAGP N RGD:5509061 20141003 MGI PMID:19965762 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21871565 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:21871565 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:23444360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:18786358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:16221970 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:22017987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:23197710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17360769 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20152175 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141030 MGI PMID:24493648 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20181004 MGI PMID:27907123 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:15314171 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:16791847 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:18641296 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000921 demyelination IAGP N RGD:5509061 20161013 MGI PMID:26656646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000921 demyelination IAGP N RGD:5509061 20170126 MGI PMID:27911893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16267821 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:20350929 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:18344997 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:23444360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:17360769 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:18202285 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:19279136 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20221124 MGI PMID:31300413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20150611 MGI PMID:23608112 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:16407399 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:18054242 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:18329011 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:21943603 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20141003 MGI PMID:18708129 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18641296 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:23197710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:23671110 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:24100213 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20190829 MGI PMID:30520996 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000959 abnormal somatic sensory system morphology IAGP N RGD:5509061 20141003 MGI PMID:16906226 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16906226 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18849985 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:23671110 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:21139565 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:23263443 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:18849985 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001003 abnormal olfactory receptor morphology IAGP N RGD:5509061 20141003 MGI PMID:24120133 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:21552476 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23946405 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16906226 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001025 abnormal sympathetic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23467373 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001034 abnormal parasympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20133851 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:24132234 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20133851 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001072 abnormal vestibulocochlear nerve morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20221124 MGI PMID:31300413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:23055936 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18849985 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:23055936 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:23055936 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20170622 MGI PMID:25043182 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20190215 MGI PMID:27018534 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:20005806 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20160811 MGI PMID:25625625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:23785158 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20005806 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23213375 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001147 small testis IAGP N RGD:5509061 20210916 MGI PMID:34355730 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220324 MGI PMID:29293683 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23213375 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220324 MGI PMID:29293683 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220714 MGI PMID:35469022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220811 MGI PMID:35574006 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20170323 MGI PMID:27345403 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20190207 MGI PMID:28292441 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:20548776 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:24191021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19618463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19897741 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19618463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001179 thick pulmonary interalveolar septum IEA N RGD:5509061 20160218 MGI 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19618463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19805914 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20180927 MGI PMID:29999500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:15784609 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:18056838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:20407033 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:17195237 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:23243018 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001192 scaly skin IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001192 scaly skin IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001192 scaly skin IAGP N RGD:5509061 20170126 MGI PMID:27435297 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001193 psoriasis IAGP N RGD:5509061 20201022 MGI PMID:32343482 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001194 dermatitis IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:17195237 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:17980593 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:21376238 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:23243018 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001200 thick skin IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:21376238 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001212 skin lesions IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001212 skin lesions IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001214 skin hyperplasia IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21376238 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20221208 MGI PMID:34620876 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:17195237 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:18262513 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:21376238 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:23243018 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001219 thick epidermis IAGP N RGD:5509061 20201022 MGI PMID:32343482 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:21376238 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20201022 MGI PMID:32343482 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16885339 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17195237 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:17195237 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:16885339 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001258 decreased body length IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20103739 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20603627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:21516099 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001260 increased body weight IAGP N RGD:5509061 20141030 MGI PMID:24374551 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15699348 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17195237 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18054242 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18327788 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18614544 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19065048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20053786 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20595581 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20603627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20660762 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21068380 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21552476 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21807948 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22469981 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22964416 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23293022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150305 MGI PMID:24646999 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170427 MGI PMID:20499347 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180208 MGI PMID:24995979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190801 MGI PMID:29029094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201022 MGI PMID:32343482 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210527 MGI PMID:32202496 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15314171 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16791847 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18641296 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19273838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20660762 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21482754 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21768369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20141016 MGI PMID:23703832 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20150219 MGI PMID:24557836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20161013 MGI PMID:26656646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20170314 MGI PMID:25952549 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20170601 MGI PMID:26544067 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20190131 MGI PMID:28846072 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20190829 MGI PMID:30520996 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20200310 MGI PMID:31469588 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001263 weight loss IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12724423 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16885339 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17418413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19906844 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19943952 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20407033 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21672919 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21962509 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22753193 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23410975 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23712803 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23918385 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24100213 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20161117 MGI PMID:27053202 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001265 decreased body size IAGP N RGD:5509061 20230511 MGI PMID:33497368 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:18693272 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:20439541 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:23817021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:20407033 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160204 MGI PMID:25180607 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160811 MGI PMID:25625625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20190516 MGI PMID:28790031 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20210506 MGI PMID:31794893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20220519 MGI PMID:34099734 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:20538915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20210506 MGI PMID:31794893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:16203745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20230511 MGI PMID:33497368 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:16203745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:17360769 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17360769 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001297 microphthalmia IAGP N RGD:5509061 20230511 MGI PMID:33497368 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20141003 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:17470285 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20141003 MGI PMID:22503753 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20150212 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16203745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23136411 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:21552476 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:23946405 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:21552476 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18641296 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:21552476 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:22609278 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:22609278 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:16203745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001341 absent eyelids IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21885734 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18518923 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19679071 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:21768369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21871565 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001393 ataxia IAGP N RGD:5509061 20161013 MGI PMID:26656646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001393 ataxia IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001393 ataxia IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001393 ataxia IAGP N RGD:5509061 20190509 MGI PMID:30305456 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:18327266 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:23293022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19270687 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20595581 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15882643 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18641296 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18832146 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20534480 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21672919 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:24311694 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141030 MGI PMID:24374551 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160623 MGI PMID:25082229 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180614 MGI PMID:26025364 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190314 MGI PMID:30429376 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200310 MGI PMID:31469588 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20201210 MGI PMID:30910745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19679071 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20534480 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20595581 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150611 MGI PMID:23608112 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180614 MGI PMID:26025364 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001405 impaired coordination IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:31469588 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001405 impaired coordination IAGP N RGD:5509061 20201210 MGI PMID:30910745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19679071 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21871565 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001406 abnormal gait IAGP N RGD:5509061 20190314 MGI PMID:30429376 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001406 abnormal gait IAGP N RGD:5509061 20190829 MGI PMID:30520996 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:19679071 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:21871565 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001407 short stride length IAGP N RGD:5509061 20181004 MGI PMID:27907123 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001407 short stride length IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:19679071 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001429 dehydration IAGP N RGD:5509061 20160623 MGI PMID:25082229 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:20603627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:18316029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18832146 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21978358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20240815 MGI PMID:38959316 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:23671110 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:20439541 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:23243018 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001505 hunched posture IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001505 hunched posture IAGP N RGD:5509061 20151224 MGI PMID:23696872 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:20407033 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20534480 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:24132234 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001513 limb grasping IAGP N RGD:5509061 20190829 MGI PMID:30520996 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:21871565 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20161013 MGI PMID:26656646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:18641296 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001523 impaired righting response IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:19679071 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:20595581 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:21871565 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:20407033 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20170216 MGI PMID:26935106 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20170810 MGI PMID:26356605 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:17448993 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:20362536 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20230810 MGI PMID:36073366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20191128 MGI PMID:23257357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17376804 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:22964416 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:24332968 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20170119 MGI PMID:27573812 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16951689 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17875932 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19075395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19805914 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22659386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20170314 MGI PMID:25952549 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20190131 MGI PMID:28846072 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001577 anemia IAGP N RGD:5509061 20210617 MGI PMID:33753942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17875932 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18927439 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16951689 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17195237 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17646578 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19261698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19415626 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20230750 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20407033 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20944627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21324922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20201022 MGI PMID:31194862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19805914 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:21193513 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20210506 MGI PMID:31794893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:23893969 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:19729436 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:19279185 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:19644017 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20170622 MGI PMID:25043182 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:20350929 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10477299 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:18171685 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:15677726 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:10477299 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:10477299 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16015321 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16267821 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:24013503 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20221006 MGI PMID:36046192 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20171109 MGI PMID:26774483 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20170622 MGI PMID:25043182 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:22534068 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:21852535 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:18029401 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:18029401 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:18029401 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20170622 MGI PMID:25043182 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10477299 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12724423 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19064922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19075395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19943952 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21962509 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23293022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23410975 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170427 MGI PMID:20499347 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220331 MGI PMID:30367465 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:19065048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24339869 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21139565 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15784609 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20360386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001785 edema IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:19075395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:24037376 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:21786402 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17463289 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:18832734 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:22613797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17923094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22613797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22613797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20170706 MGI PMID:26116508 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20170525 MGI PMID:26061883 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20170706 MGI PMID:26116508 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16951689 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17536012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22916024 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141120 MGI PMID:25053428 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20150205 MGI PMID:24715454 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16951689 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17923094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:19351896 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:20439541 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:22075698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20150219 MGI PMID:24241423 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20161013 MGI PMID:26656646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001844 autoimmune response IAGP N RGD:5509061 20161013 MGI PMID:26656646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:24135136 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20160519 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:18641296 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:23293291 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20150219 MGI PMID:24557836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:18037992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:21724990 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23966625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001874 acanthosis IAGP N RGD:5509061 20201022 MGI PMID:32343482 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:21139565 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20360386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20363774 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20407033 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20439995 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141016 MGI PMID:24361262 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20150212 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21266350 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21324922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21482677 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001884 mammary gland alveolar hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21266350 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001884 mammary gland alveolar hyperplasia IAGP N RGD:5509061 20201022 MGI PMID:31194862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001889 delayed brain development IAGP N RGD:5509061 20141003 MGI PMID:18029401 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20151224 MGI PMID:23696872 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19279185 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19415626 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22659386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160623 MGI PMID:24520391 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001914 hemorrhage IAGP N RGD:5509061 20171109 MGI PMID:26774483 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001914 hemorrhage IAGP N RGD:5509061 20230511 MGI PMID:33497368 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:15784609 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20151112 MGI PMID:23358455 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001921 reduced fertility IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20170622 MGI PMID:25043182 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:21482754 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001924 infertility IAGP N RGD:5509061 20190801 MGI PMID:29029094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23819925 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:24100213 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001925 male infertility IAGP N RGD:5509061 20160519 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001925 male infertility IAGP N RGD:5509061 20181025 MGI PMID:28723571 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001925 male infertility IAGP N RGD:5509061 20220811 MGI PMID:35574006 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20808952 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:21516099 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001926 female infertility IAGP N RGD:5509061 20190215 MGI PMID:27018534 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:21516099 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21807948 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23410975 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001935 decreased litter size IAGP N RGD:5509061 20170622 MGI PMID:25043182 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:17047082 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:22964416 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001947 abnormal mucociliary clearance IAGP N RGD:5509061 20141003 MGI PMID:19675306 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20161117 MGI PMID:27053202 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:20534480 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:20548776 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001954 respiratory distress IAGP N RGD:5509061 20181004 MGI PMID:27907123 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001956 hypopnea IAGP N RGD:5509061 20161117 MGI PMID:27053202 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001958 emphysema IAGP N RGD:5509061 20180927 MGI PMID:29999500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001967 deafness IAGP N RGD:5509061 20180712 MGI PMID:27660326 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:18249134 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:18249134 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21139565 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:23263443 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:22986526 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:19061836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20160728 MGI PMID:25377472 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20180830 MGI PMID:21795710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16015321 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17418413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18043744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19064922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19321799 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19351831 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21324922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22574128 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23243018 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23410975 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20150903 MGI PMID:25453902 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:18621715 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16015321 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21441929 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22897848 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20170921 MGI PMID:26668357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16015321 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18043744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20439541 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21324922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21685933 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22393458 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20180906 MGI PMID:25565005 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:17875932 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:20947725 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21093323 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21441929 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20151217 MGI PMID:24440599 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20161124 MGI PMID:26304963 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20180906 MGI PMID:25565005 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20190131 MGI PMID:28846072 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19064922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20548776 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22430205 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20160602 MGI PMID:22863881 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17418413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19351831 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20947725 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21512139 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23281395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20150903 MGI PMID:25453902 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17047082 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19064922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20947725 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22574128 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23453624 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002039 increased neuroblastoma incidence IAGP N RGD:5509061 20180913 MGI PMID:23042116 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002039 increased neuroblastoma incidence IAGP N RGD:5509061 20180913 MGI PMID:25174395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19061836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19064922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:19710174 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16054034 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:18262513 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:23243018 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:22017987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002064 seizures IAGP N RGD:5509061 20161013 MGI PMID:26656646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002064 seizures IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20170413 MGI PMID:26896819 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20181004 MGI PMID:27907123 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:21248239 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:16885339 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:21376238 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:20880997 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20190110 MGI PMID:27134165 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17992256 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18316029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20191128 MGI PMID:23257357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17992256 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21441927 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21962509 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:24332968 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20170119 MGI PMID:27573812 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20190314 MGI PMID:30429376 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19679071 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20230302 MGI PMID:32552404 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15784609 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16015321 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16791847 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16951689 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17047082 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17418413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17875932 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17980593 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18056838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18536716 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18621715 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18691547 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18693272 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19064922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19092805 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19251594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19273838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19321799 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19351831 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19805914 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20404087 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20439541 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20548776 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20947725 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21093323 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21193513 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21324922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21367862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21441929 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21482677 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21482754 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21625383 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21672919 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22232209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22363786 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22393458 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22574128 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22699621 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22897848 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23077666 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23243018 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23281395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23410975 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23502960 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23817021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23893969 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23966625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24121508 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20141016 MGI PMID:24411941 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20150611 MGI PMID:23608112 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20151112 MGI PMID:22185780 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20151217 MGI PMID:24440599 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20151224 MGI PMID:23696872 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20160602 MGI PMID:22863881 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20160728 MGI PMID:25377472 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20160929 MGI PMID:25787764 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20161013 MGI PMID:26656646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20161124 MGI PMID:26304963 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20170314 MGI PMID:25952549 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20170601 MGI PMID:26544067 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20170810 MGI PMID:26356605 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20180614 MGI PMID:26025364 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20180906 MGI PMID:25565005 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20181004 MGI PMID:27907123 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20181025 MGI PMID:28723571 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20190131 MGI PMID:28846072 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20190516 MGI PMID:28790031 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20190801 MGI PMID:29029094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20191205 MGI PMID:31685994 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:31469588 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20201022 MGI PMID:32343482 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20201210 MGI PMID:30910745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20210520 MGI PMID:24280485 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20220519 MGI PMID:34099734 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002083 premature death IAGP N RGD:5509061 20241024 MGI PMID:31048544 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17418413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10477299 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:17360769 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:23293291 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20150212 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:21672919 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20200310 MGI PMID:31469588 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21828091 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:19386268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:23410975 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:17164415 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:19386268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:16885339 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20240229 MGI PMID:30661984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20151112 MGI PMID:23358455 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:23671110 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22190459 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20180111 MGI PMID:27480224 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18056838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22659386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20160414 MGI PMID:25965570 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20170216 MGI PMID:26935106 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20241107 MGI PMID:35477278 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:19675306 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:23502960 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141030 MGI PMID:24700869 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:20562878 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:20619750 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20929728 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20439541 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22523384 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23230003 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23293358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18198335 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20350929 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20151224 MGI PMID:23696872 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180329 MGI PMID:29033352 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:11130972 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:20947725 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12163453 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12657690 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14657333 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14717328 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15882628 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15941831 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16267821 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16373502 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16791847 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16896181 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16906226 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17035522 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17171761 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17225864 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17304540 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17868096 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17992256 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18161057 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18344997 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18347334 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18395834 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18395835 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18395839 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18801387 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19093031 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19155467 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19172189 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19279185 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19332644 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19497281 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19551907 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19630976 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19692579 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19924248 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20010831 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20023653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20053786 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20652949 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20880997 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21324922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21445964 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21482754 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21504045 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21768369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21807948 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21852535 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21896734 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22155527 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22243745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22253858 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22343123 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22467513 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22659386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22884371 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23175634 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23293022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23352170 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23441035 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23824573 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24003143 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24311694 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24431991 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24569379 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9108056 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9916792 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151001 MGI PMID:15282743 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160204 MGI PMID:25180607 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180517 MGI PMID:29180569 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20181122 MGI PMID:29538372 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210527 MGI PMID:32202496 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25377472 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:34767447 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:21238928 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20944627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23238710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:15882643 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002183 gliosis IAGP N RGD:5509061 20200423 MGI PMID:30142928 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:20818386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:23277569 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:23444360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:19415626 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:17195237 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20241107 MGI PMID:35477278 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:16525473 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:18940590 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:23141534 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20190509 MGI PMID:30305456 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20240815 MGI PMID:38959316 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20160519 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23712803 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:15882643 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22401858 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20221124 MGI PMID:31300413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20221124 MGI PMID:31300413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20180927 MGI PMID:29999500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20595581 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20818386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21907138 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23041622 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23374353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:24177424 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20160623 MGI PMID:25807280 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002281 abnormal respiratory mucosa goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21724990 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:17875932 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002347 abnormal lymph node T cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:18354198 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002367 abnormal thymus lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:17536012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:17536012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:19351896 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22392989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22659386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22659386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20191017 MGI PMID:29625069 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18927439 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18056424 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19251594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17536012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:16951689 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20240613 MGI PMID:38329807 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:17875932 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20151224 MGI PMID:24498102 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18504307 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20150219 MGI PMID:24241423 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23243279 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16782029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18832734 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20210826 MGI PMID:33336366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:19075395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16230473 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20170706 MGI PMID:26116508 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:21724990 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002493 increased IgG level IAGP N RGD:5509061 20240613 MGI PMID:38329807 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002494 increased IgM level IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20190314 MGI PMID:30429376 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:23455710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:19075395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002606 increased basophil cell number IAGP N RGD:5509061 20161124 MGI PMID:26304963 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18056838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:24121508 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20150219 MGI PMID:24557836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:22883231 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20170119 MGI PMID:27573812 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180111 MGI PMID:27480224 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20191128 MGI PMID:23257357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20160519 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002632 vestigial tail IAGP N RGD:5509061 20141003 MGI PMID:16791847 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:17344228 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141030 MGI PMID:24493648 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16885339 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:21930934 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20160519 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20180517 MGI PMID:29180569 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:18396135 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:18518923 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23819925 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20191003 MGI PMID:31383820 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220428 MGI PMID:33476744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002676 uterus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19710174 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21807948 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20191003 MGI PMID:31383820 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:22146645 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002695 abnormal circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:17470285 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:20299358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23502960 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20220331 MGI PMID:30367465 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:20299358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002711 decreased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:22764048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:19065048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20150129 MGI PMID:24504341 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15699348 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18316029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19065048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:24332968 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20191128 MGI PMID:23257357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200310 MGI PMID:31469588 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200416 MGI PMID:32092075 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002735 abnormal chemical nociception IAGP N RGD:5509061 20141003 MGI PMID:18249134 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002735 abnormal chemical nociception IAGP N RGD:5509061 20141003 MGI PMID:21139565 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20190509 MGI PMID:30305456 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18297725 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:23619366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20160107 MGI PMID:26100917 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002750 exophthalmos IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:21068380 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20201119 MGI PMID:31819041 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20180614 MGI PMID:26025364 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20190314 MGI PMID:30429376 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20200310 MGI PMID:31469588 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:23100420 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002764 short tibia IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002764 short tibia IAGP N RGD:5509061 20220908 MGI PMID:33105483 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:17164415 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002765 short fibula IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22975327 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23029280 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23136411 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23918385 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20160310 MGI PMID:25198863 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20170314 MGI PMID:23911327 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20210729 MGI PMID:27464479 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170810 MGI PMID:26356605 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170824 MGI PMID:20733101 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:18832146 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:20025862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002833 increased heart weight IAGP N RGD:5509061 20160929 MGI PMID:25787764 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17470285 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21091282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:24327562 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:21552476 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:23946405 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:15784609 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:22326220 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:23502960 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:18056838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:24121508 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:16951689 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19075395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20959632 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23455710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20161124 MGI PMID:26304963 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20170314 MGI PMID:25952549 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20170601 MGI PMID:26544067 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20210617 MGI PMID:33753942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16951689 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17875932 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20959632 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23455710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20170314 MGI PMID:25952549 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20170601 MGI PMID:26544067 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20210617 MGI PMID:33753942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20190829 MGI PMID:30520996 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21768369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21978358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22017987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22120178 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20151224 MGI PMID:23696872 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20201210 MGI PMID:30910745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:18029401 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20210121 MGI PMID:33127760 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:23141534 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21962509 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20180208 MGI PMID:24995979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20191128 MGI PMID:23257357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200416 MGI PMID:32092075 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:22792209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002902 decreased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:19729436 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:21593206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19679071 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20223200 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20240815 MGI PMID:38959316 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20141003 MGI PMID:18693272 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:19551907 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:19551907 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002933 joint inflammation IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002936 joint swelling IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:18693272 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002938 white spotting IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:15314171 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20935052 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15882643 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:24179230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:19064922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20160811 MGI PMID:26806701 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19092805 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20200409 MGI PMID:31588799 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20220331 MGI PMID:30367465 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002965 increased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20170119 MGI PMID:27573812 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20170216 MGI PMID:26935106 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002975 vascular smooth muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17195237 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19551907 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22883231 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002981 increased liver weight IAGP N RGD:5509061 20161124 MGI PMID:26304963 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002981 increased liver weight IAGP N RGD:5509061 20170119 MGI PMID:27573812 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:17075007 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:19729436 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:20299358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:21343368 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:24656820 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002989 small kidney IAGP N RGD:5509061 20150625 MGI PMID:24732380 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:20005806 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003010 decreased mortality induced by ionizing radiation IAGP N RGD:5509061 20210506 MGI PMID:31794893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003022 increased coronary flow rate IAGP N RGD:5509061 20201119 MGI PMID:18312674 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:24091011 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:18312674 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:22753193 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20150219 MGI PMID:24899231 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20240620 MGI PMID:35680100 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:23263443 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003046 liver cirrhosis IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003052 omphalocele IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:20152175 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003054 spina bifida IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22155527 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20221124 MGI PMID:31300413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003057 abnormal epicardium morphology IAGP N RGD:5509061 20141003 MGI PMID:21311046 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19065048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:22764048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20200416 MGI PMID:32092075 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:22753193 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141016 MGI PMID:24048525 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20141016 MGI PMID:24048525 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17164415 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:21555590 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18160036 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:21482754 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:21930934 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:23975099 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20170629 MGI PMID:26919979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20230810 MGI PMID:36073366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20181004 MGI PMID:27907123 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18331721 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21068380 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20181004 MGI PMID:27907123 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:10477299 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:20350929 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:18037992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:16203745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:15314171 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:17164415 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:22792209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003109 short femur IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003109 short femur IAGP N RGD:5509061 20220908 MGI PMID:33105483 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19075002 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:20404087 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:12185368 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003124 hypospadia IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003129 persistent cloaca IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003130 anal atresia IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:20570943 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20733101 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21193513 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20170216 MGI PMID:26935106 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003154 abnormal soft palate morphology IAGP N RGD:5509061 20221027 MGI PMID:34557486 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:16951689 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23435463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20170314 MGI PMID:25952549 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20190131 MGI PMID:28846072 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20220714 MGI PMID:35469022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21871565 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:23213375 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003213 decreased susceptibility to age related obesity IAGP N RGD:5509061 20141030 MGI PMID:24374551 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17195237 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20160929 MGI PMID:25787764 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20170105 MGI PMID:27812542 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20201119 MGI PMID:31819041 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20160929 MGI PMID:25787764 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18029401 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19415626 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22659386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20223200 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22914740 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20160317 MGI PMID:25174890 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:21768369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003248 loss of glutamate neurons IAGP N RGD:5509061 20141003 MGI PMID:18198335 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20201022 MGI PMID:31194862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003266 biliary cyst IAGP N RGD:5509061 20201022 MGI PMID:31194862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:16015321 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:20363774 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003288 intestinal edema IAGP N RGD:5509061 20150219 MGI PMID:24557836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20141003 MGI PMID:23535651 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003292 melena IAGP N RGD:5509061 20141003 MGI PMID:19805914 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:17047082 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20170525 MGI PMID:26061883 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19234449 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003326 liver failure IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:20811458 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:22399757 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19234449 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141016 MGI PMID:23703832 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:14657333 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:19065048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:23382704 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22401858 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003359 hypaxial muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20170216 MGI PMID:26935106 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16690964 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003397 increased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:15485899 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003398 increased skeletal muscle size IAGP N RGD:5509061 20141003 MGI PMID:15485899 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20230750 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:21852535 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:19906844 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12724423 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:19906844 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:19321799 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003418 premature intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19047372 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20180517 MGI PMID:29180569 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:21715642 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:22522171 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:23444360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:17360769 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003427 parakeratosis IAGP N RGD:5509061 20201022 MGI PMID:32343482 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20040494 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20220331 MGI PMID:30367465 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20233865 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20191205 MGI PMID:31685994 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20210506 MGI PMID:31794893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20210520 MGI PMID:24280485 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:23202126 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:23410975 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17980593 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20025862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23222438 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20141003 MGI PMID:17980593 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20141003 MGI PMID:23453624 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:18327266 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:21035764 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:20595581 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003496 increased thyroid adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003531 abnormal vagina development IAGP N RGD:5509061 20141003 MGI PMID:21516099 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19065048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24332968 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20220804 MGI PMID:35472723 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20180301 MGI PMID:28698371 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20160811 MGI PMID:25625625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003580 increased fibroma incidence IAGP N RGD:5509061 20141003 MGI PMID:19321799 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003587 ureter obstruction IAGP N RGD:5509061 20160714 MGI PMID:25194568 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003596 epididymis inflammation IAGP N RGD:5509061 20160519 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:23817021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141030 MGI PMID:24523320 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20161013 MGI PMID:26656646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:24267650 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20201210 MGI PMID:30910745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:21978358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:23535651 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:19618463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:24191021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:15784609 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20150219 MGI PMID:24557836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20151224 MGI PMID:24498102 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20190131 MGI PMID:28846072 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141204 MGI PMID:25105579 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003647 absent oligodendrocytes IAGP N RGD:5509061 20141003 MGI PMID:15314171 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003647 absent oligodendrocytes IAGP N RGD:5509061 20141003 MGI PMID:16407399 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003647 absent oligodendrocytes IAGP N RGD:5509061 20141003 MGI PMID:16791847 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22017987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:21185281 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:17646578 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:20944627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:21852535 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:12724423 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:19906844 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19064922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21441929 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003674 oxidative stress IAGP N RGD:5509061 20170216 MGI PMID:26935106 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:23502960 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003675 kidney cyst IAGP N RGD:5509061 20150625 MGI PMID:24732380 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003675 kidney cyst IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20230831 MGI PMID:34004180 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:21593206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003707 increased cell nucleus count IAGP N RGD:5509061 20201015 MGI PMID:32269212 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:19279185 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:24013503 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20944627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20210729 MGI PMID:27464479 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:20152175 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:18056424 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20852630 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21625383 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22430205 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23243018 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23410975 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20210506 MGI PMID:31794893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:23619366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17301087 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20150212 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21552476 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003760 decreased palatal length IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:21852535 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22155527 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22792209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003798 abnormal Harderian gland pigmentation IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:20412777 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003818 abnormal eye muscle development IAGP N RGD:5509061 20141003 MGI PMID:16203745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003826 abnormal Mullerian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16054034 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:21828091 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003840 abnormal coronal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:17523175 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20190215 MGI PMID:27018534 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:24132234 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003853 dry skin IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003853 dry skin IAGP N RGD:5509061 20170126 MGI PMID:27435297 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003865 lymph node inflammation IAGP N RGD:5509061 20161013 MGI PMID:26656646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:19729436 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141030 MGI PMID:24493648 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003872 absent heart right ventricle IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19415626 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20171109 MGI PMID:26774483 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003877 abnormal serotonergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20818386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003878 abnormal ear physiology IAGP N RGD:5509061 20141003 MGI PMID:19679071 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:23893969 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22401858 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19551907 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:21193513 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141030 MGI PMID:24700869 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21145505 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20733101 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21068380 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003928 increased heart rate variability IAGP N RGD:5509061 20141003 MGI PMID:21193513 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:12185368 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:14657333 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:17938243 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:21205788 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:22529374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:22964416 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20151112 MGI PMID:23358455 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003948 abnormal gas homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:22792209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10477299 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18029401 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21505259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21852535 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24013503 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18037992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:18054242 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17195237 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17646578 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19805914 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19850870 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21552476 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23136411 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21552476 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23136411 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20141003 MGI PMID:19075002 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20141003 MGI PMID:21266350 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:21266350 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004024 aneuploidy IAGP N RGD:5509061 20200409 MGI PMID:31588799 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:21266350 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:19075002 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20404087 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20571512 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:23975099 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20170629 MGI PMID:26919979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20171109 MGI PMID:26774483 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004049 increased acute promyelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21441929 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:21311046 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:20350929 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:16690964 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:21068380 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19363146 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23142661 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:22914740 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004106 lymphatic vessel hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20407033 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23178125 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004115 abnormal sinoatrial node morphology IAGP N RGD:5509061 20141003 MGI PMID:21193513 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20170216 MGI PMID:26935106 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:20660762 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20221027 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20221124 MGI PMID:31300413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:21768369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23945236 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20181227 MGI PMID:30204862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004149 increased bone strength IAGP N RGD:5509061 20181227 MGI PMID:30204862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:20570943 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:24100213 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004165 abnormal lateral geniculate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19357274 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:23671110 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:18327788 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20221006 MGI PMID:36046192 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:16015321 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16885339 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17047082 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19321799 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20233865 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:19906844 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20160929 MGI PMID:25787764 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20170216 MGI PMID:26935106 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004226 absent Schlemm's canal IAGP N RGD:5509061 20150212 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17967868 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20170601 MGI PMID:26544067 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20201119 MGI PMID:31819041 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:22232209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20170622 MGI PMID:25043182 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:21852535 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:16203745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:24132234 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20180405 MGI PMID:29033352 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:23077666 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20151224 MGI PMID:23696872 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:18329011 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004298 vestibular ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004315 absent vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004349 absent femur IAGP N RGD:5509061 20141003 MGI PMID:17164415 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20171221 MGI PMID:28899994 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20191212 MGI PMID:29961578 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004369 absent utricle IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004371 bowed femur IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004377 small frontal bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004377 small frontal bone IAGP N RGD:5509061 20171102 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004377 small frontal bone IAGP N RGD:5509061 20210121 MGI PMID:33127760 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004380 short frontal bone IAGP N RGD:5509061 20141003 MGI PMID:15699348 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20190110 MGI PMID:27134165 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004383 absent interparietal bone IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23243279 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004441 small occipital bone IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004454 absent pterygoid process IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004458 absent alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004460 alisphenoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004470 small nasal bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004470 small nasal bone IAGP N RGD:5509061 20150910 MGI PMID:24895408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:15699348 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:17523175 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004481 abnormal conjunctival epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23293291 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20170907 MGI PMID:26436652 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:18043744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23410975 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20160519 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20171214 MGI PMID:28319059 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11130972 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:24656820 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20200409 MGI PMID:31588799 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004506 abnormal pubis morphology IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17164415 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20171221 MGI PMID:28899994 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20180712 MGI PMID:27660326 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004520 short vestibular hair cell stereocilia IAGP N RGD:5509061 20171221 MGI PMID:28899994 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20180712 MGI PMID:27660326 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004523 decreased cochlear hair cell stereocilia number IAGP N RGD:5509061 20171221 MGI PMID:28899994 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20180712 MGI PMID:27660326 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004536 short inner hair cell stereocilia IAGP N RGD:5509061 20180712 MGI PMID:27660326 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004539 absent maxilla IAGP N RGD:5509061 20141003 MGI PMID:22190459 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004540 small maxilla IAGP N RGD:5509061 20210121 MGI PMID:33127760 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004562 abnormal inner hair cell synaptic ribbon morphology IAGP N RGD:5509061 20141003 MGI PMID:24327562 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20160929 MGI PMID:25787764 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20170216 MGI PMID:26935106 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004592 small mandible IAGP N RGD:5509061 20210121 MGI PMID:33127760 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:23671110 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:22792209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004614 caudal vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:24091011 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:24091011 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:24091011 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:23671110 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:24091011 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004648 decreased thoracic vertebrae number IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004653 absent caudal vertebrae IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004657 small sacral vertebrae IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:19906844 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20180517 MGI PMID:29180569 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004708 short lumbar vertebrae IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004712 notochord degeneration IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004714 truncated notochord IAGP N RGD:5509061 20141003 MGI PMID:20350929 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004714 truncated notochord IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:23435463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:23408898 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16054034 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004755 abnormal loop of Henle morphology IAGP N RGD:5509061 20141030 MGI PMID:24700869 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20171109 MGI PMID:26774483 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:19075002 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20170629 MGI PMID:26919979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20241024 MGI PMID:31048544 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23619366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:21768369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20190829 MGI PMID:30520996 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:19679071 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20210701 MGI PMID:33524375 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:19415626 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:18832734 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:20005806 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22606246 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20161124 MGI PMID:26304963 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:17448993 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23230003 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20151112 MGI PMID:22185780 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20190131 MGI PMID:28846072 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20190418 MGI PMID:30692594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141218 MGI PMID:24501354 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20190620 MGI PMID:27253061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:22547703 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:21613984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22547703 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22869596 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:22897848 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20210513 MGI PMID:33526923 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20231102 MGI PMID:35439434 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:20215352 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20190314 MGI PMID:30429376 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004831 long incisors IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:19273838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22902753 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:23222438 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18372904 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:23222438 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24339869 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21807948 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23213375 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210916 MGI PMID:34355730 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:21516099 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:19060336 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004880 lung cyst IAGP N RGD:5509061 20141003 MGI PMID:24191021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004880 lung cyst IAGP N RGD:5509061 20200430 MGI PMID:21309069 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20160623 MGI PMID:24520391 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20160623 MGI PMID:25082229 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20230810 MGI PMID:36073366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141030 MGI PMID:24374551 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20150305 MGI PMID:24646999 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20180208 MGI PMID:24995979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20200310 MGI PMID:31469588 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20190215 MGI PMID:27018534 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220324 MGI PMID:29293683 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20160728 MGI PMID:25377472 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:23785158 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004922 abnormal common crus morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:21807948 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20160519 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:20040494 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:20299358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:17646578 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20210513 MGI PMID:33526923 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004941 abnormal regulatory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21468021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23065717 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:19075395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004947 skin inflammation IAGP N RGD:5509061 20201022 MGI PMID:32343482 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:19965762 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:22017987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20210520 MGI PMID:24280485 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21555590 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23918385 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:24121508 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20161124 MGI PMID:26304963 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20151112 MGI PMID:22185780 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20170525 MGI PMID:26061883 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004958 enlarged prostate gland IAGP N RGD:5509061 20141003 MGI PMID:23817021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004961 increased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004972 abnormal regulatory T cell number IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23966625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18354198 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23065717 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:17923094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:22017987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:18198335 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:23444360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:22792209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:22792209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20181227 MGI PMID:30204862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:23945236 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:22792209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20181227 MGI PMID:30204862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21724990 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22138715 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23630390 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16782029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19879843 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23619366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005014 increased B cell number IAGP N RGD:5509061 20150219 MGI PMID:24241423 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005014 increased B cell number IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005014 increased B cell number IAGP N RGD:5509061 20170921 MGI PMID:26668357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005015 increased T cell number IAGP N RGD:5509061 20150205 MGI PMID:24715454 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005015 increased T cell number IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17923094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18354198 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20151112 MGI PMID:22185780 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20170314 MGI PMID:25952549 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20170601 MGI PMID:26544067 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15314171 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21093323 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23230003 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:24591644 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170525 MGI PMID:26061883 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20170706 MGI PMID:26116508 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20190131 MGI PMID:28846072 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20439541 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20932862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20190131 MGI PMID:28846072 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:21593206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:16230473 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:16230473 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:18354198 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:22138715 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21852535 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:10477299 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21852535 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005036 diarrhea IAGP N RGD:5509061 20150219 MGI PMID:24557836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005036 diarrhea IAGP N RGD:5509061 20160623 MGI PMID:25082229 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18037992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24191021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20170629 MGI PMID:26919979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:24339869 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16951689 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20190131 MGI PMID:28846072 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18354198 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20439541 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22916024 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20190131 MGI PMID:28846072 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22547703 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24244019 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20170706 MGI PMID:26116508 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005100 abnormal choroid pigmentation IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16203745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005114 premature hair loss IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:18614544 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20190801 MGI PMID:29029094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21068380 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160929 MGI PMID:25787764 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170406 MGI PMID:26039991 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170810 MGI PMID:26356605 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20201119 MGI PMID:31819041 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:19805914 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:20439541 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:22401858 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005150 cachexia IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005150 cachexia IAGP N RGD:5509061 20151224 MGI PMID:23696872 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005152 pancytopenia IAGP N RGD:5509061 20170314 MGI PMID:25952549 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005152 pancytopenia IAGP N RGD:5509061 20170601 MGI PMID:26544067 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20170921 MGI PMID:26668357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:23213375 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005159 azoospermia IAGP N RGD:5509061 20181025 MGI PMID:28723571 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005159 azoospermia IAGP N RGD:5509061 20210916 MGI PMID:34355730 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005159 azoospermia IAGP N RGD:5509061 20220324 MGI PMID:29293683 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005159 azoospermia IAGP N RGD:5509061 20220811 MGI PMID:35574006 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:23238710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20220519 MGI PMID:29396429 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22232209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:23238710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:24132234 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:18037992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005174 abnormal tail pigmentation IEA N RGD:5509061 20211118 MGI 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20210304 MGI PMID:30646909 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15699348 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20210701 MGI PMID:33524375 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20230810 MGI PMID:36073366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005191 head tilt IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20150212 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005197 abnormal uvea morphology IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19850870 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21552476 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23136411 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:20439541 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:22401858 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005202 lethargy IAGP N RGD:5509061 20141016 MGI PMID:23703832 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:19065048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:20364121 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:22964416 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19065048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19065048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:14657333 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:19357274 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:21238928 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005238 increased brain size IAGP N RGD:5509061 20151224 MGI PMID:23696872 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005238 increased brain size IAGP N RGD:5509061 20180329 MGI PMID:29033352 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22063212 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22609278 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:21311046 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20150212 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20230413 MGI PMID:32440726 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005257 abnormal intraocular pressure IAGP N RGD:5509061 20150212 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:17470285 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15987751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:23502960 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20200409 MGI PMID:31588799 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20220331 MGI PMID:30367465 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20150430 MGI PMID:24622775 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20180830 MGI PMID:27124591 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20161117 MGI PMID:27053202 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:15699348 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:18316029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:24332968 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141030 MGI PMID:24374551 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20180208 MGI PMID:24995979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:23028821 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20170810 MGI PMID:26356605 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20210729 MGI PMID:29861389 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17992256 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18316029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21962509 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20150305 MGI PMID:24646999 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180208 MGI PMID:24995979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200416 MGI PMID:32092075 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21035764 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21441927 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21962509 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20231109 MGI PMID:36325906 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005305 prostate gland anterior lobe hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:27020859 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005307 head tossing IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005310 abnormal salivary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:19788412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:18029401 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22883231 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15699348 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:16906226 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005324 ascites IAGP N RGD:5509061 20141016 MGI PMID:23703832 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005324 ascites IAGP N RGD:5509061 20181004 MGI PMID:27907123 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:15987751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17646578 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:23502960 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15987751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17376804 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21441927 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005331 insulin resistance IAGP N RGD:5509061 20170119 MGI PMID:27573812 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:21193513 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20161117 MGI PMID:27053202 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20230810 MGI PMID:36073366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:15314171 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20439541 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21724990 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005385 cardiovascular system phenotype IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:20595581 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:20818386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141030 MGI PMID:24493648 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19679071 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20190829 MGI PMID:30520996 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:15314171 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:16791847 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005405 axon degeneration IAGP N RGD:5509061 20161013 MGI PMID:26656646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005405 axon degeneration IAGP N RGD:5509061 20190829 MGI PMID:30520996 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005408 hypopigmentation IEA N RGD:5509061 20211118 MGI 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20170427 MGI PMID:20499347 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005424 jerky movement IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:22753193 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005430 absent fibula IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:20660762 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20150305 MGI PMID:24646999 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18354198 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:16230473 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:16230473 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20190801 MGI PMID:29029094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20190801 MGI PMID:29029094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005473 decreased triiodothyronine level IAGP N RGD:5509061 20190801 MGI PMID:29029094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:15699348 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141030 MGI PMID:24374551 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:15699348 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20161124 MGI PMID:26304963 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005488 bronchial epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20548776 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005493 stomach epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:20215352 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:17875932 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12724423 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16791847 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:20215352 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141016 MGI PMID:23703832 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20170427 MGI PMID:20499347 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005535 abnormal body temperature IAGP N RGD:5509061 20141003 MGI PMID:18249134 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:17470285 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:23293291 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20230810 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005546 choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:20880997 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20160526 MGI PMID:23136411 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20141003 MGI PMID:19850870 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21552476 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23136411 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20151224 MGI PMID:26287463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19065048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21962509 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15699348 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18316029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:31469588 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20201022 MGI PMID:32343482 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:23455710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:19075395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:18056838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141030 MGI PMID:24700869 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005575 increased pulmonary ventilation IAGP N RGD:5509061 20161117 MGI PMID:27053202 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16940357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20190801 MGI PMID:29029094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005585 increased tidal volume IAGP N RGD:5509061 20161117 MGI PMID:27053202 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21555590 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20733101 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17646578 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20733101 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:22753193 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20230511 MGI PMID:33497368 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20230511 MGI PMID:33497368 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005603 neuron hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21238928 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:23945236 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005605 increased bone mass IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005605 increased bone mass IAGP N RGD:5509061 20170427 MGI PMID:20499347 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22094252 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22344573 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23132912 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20160512 MGI PMID:25770585 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20170518 MGI PMID:25737282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20170810 MGI PMID:26356605 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:19630976 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:20223200 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20190801 MGI PMID:29029094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:17164415 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22883231 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:23028821 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15699348 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:21962509 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20170119 MGI PMID:27573812 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200416 MGI PMID:32092075 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005661 decreased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:18316029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005664 decreased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:18316029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005665 increased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:19630976 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22883231 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20150305 MGI PMID:24646999 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23293291 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:23535651 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:19270687 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20180517 MGI PMID:29180569 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:21091282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:22859504 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20181004 MGI PMID:27907123 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20211209 MGI PMID:33753492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20220428 MGI PMID:33476744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:21091282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:21768369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20170126 MGI PMID:27911893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20170810 MGI PMID:26356605 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20240620 MGI PMID:35680100 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20141003 MGI PMID:21068380 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006039 decreased mitochondrial fission IAGP N RGD:5509061 20211209 MGI PMID:33753492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19061836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19075002 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20151224 MGI PMID:24498102 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20240613 MGI PMID:33517884 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21565614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20210506 MGI PMID:31794893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:15784609 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19023080 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:19261698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:18347334 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20230413 MGI PMID:35169021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17301087 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20161013 MGI PMID:26656646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20141003 MGI PMID:19805914 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20160623 MGI PMID:24520391 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006093 arteriovenous malformation IAGP N RGD:5509061 20160623 MGI PMID:25082229 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006095 absent amacrine cells IAGP N RGD:5509061 20141003 MGI PMID:17301087 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20141003 MGI PMID:17537797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:15789410 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:17344228 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:21185281 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:21597012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20160811 MGI PMID:26806701 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231102 MGI PMID:35899771 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20170216 MGI PMID:26935106 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20150212 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:19644017 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20141003 MGI PMID:21311046 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:18545654 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:21266350 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:21482677 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:19386268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:23213437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20151112 MGI PMID:23358455 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20141003 MGI PMID:20350929 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20151112 MGI PMID:23358455 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:20346763 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16015321 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17047082 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18691547 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19064922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22574128 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20210520 MGI PMID:24280485 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20240404 MGI PMID:38517960 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006292 abnormal nasal placode morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:20363774 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20171109 MGI PMID:26774483 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22609278 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20150212 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006306 abnormal nasal pit morphology IAGP N RGD:5509061 20230309 MGI PMID:23872235 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:18545654 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006321 increased myocardial fiber number IAGP N RGD:5509061 20160929 MGI PMID:25787764 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006322 abnormal perichondrium morphology IAGP N RGD:5509061 20141003 MGI PMID:19906844 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006325 impaired hearing IAGP N RGD:5509061 20191212 MGI PMID:29961578 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006334 abnormal susceptibility to hearing loss IAGP N RGD:5509061 20141003 MGI PMID:23408898 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:22190459 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23221368 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20220324 MGI PMID:29293683 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:21807948 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210916 MGI PMID:34355730 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220428 MGI PMID:33476744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:19906844 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006408 dorsal root ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18849985 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006408 dorsal root ganglion hypoplasia IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18566418 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21421856 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21724990 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20160811 MGI PMID:25625625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:18160036 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20571512 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21191184 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21482754 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21930934 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:17047082 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:18043744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17456738 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18264106 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19010921 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19061836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20160602 MGI PMID:22863881 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008021 increased blastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20161013 MGI PMID:26656646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008031 decreased Cajal-Retzius cell number IAGP N RGD:5509061 20141003 MGI PMID:19805388 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20191128 MGI PMID:23257357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21421856 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:18354198 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23430111 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22875805 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20538915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18786358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:17967868 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:18160036 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:22326220 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:23502960 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008071 absent B cells IAGP N RGD:5509061 20161124 MGI PMID:27303042 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20150219 MGI PMID:24241423 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17923094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18354198 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23293358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23727894 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20150219 MGI PMID:24241423 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17923094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18354198 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22875805 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18354198 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20439541 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:23966625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21468021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008094 absent memory B cells IAGP N RGD:5509061 20141003 MGI PMID:20929728 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20170921 MGI PMID:26668357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20210826 MGI PMID:33336366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20210826 MGI PMID:33336366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21613984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:19273838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:20404087 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:22354172 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008112 abnormal monocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19110448 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24591644 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:24591644 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20190131 MGI PMID:28846072 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20201022 MGI PMID:32343482 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:24591644 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20170706 MGI PMID:26116508 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20170525 MGI PMID:26061883 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:22326220 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:23502960 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20200409 MGI PMID:31588799 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18832146 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141218 MGI PMID:24501354 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:18331721 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008156 decreased diameter of tibia IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008162 increased diameter of tibia IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008166 abnormal B-2 B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:21708930 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008172 abnormal follicular B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:24244019 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:24244019 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:17463289 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:22897848 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:23619366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:20929728 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20170525 MGI PMID:26061883 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20170706 MGI PMID:26116508 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008179 absent germinal center B cells IAGP N RGD:5509061 20141003 MGI PMID:20929728 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:24244019 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20170525 MGI PMID:26061883 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008185 decreased naive B cell number IAGP N RGD:5509061 20141003 MGI PMID:20929728 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:23133585 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22613797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:17923094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:23230003 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:23133585 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:23230003 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17923094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18663224 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:19879843 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008213 absent immature B cells IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16980619 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:17536012 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:23230003 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20170921 MGI PMID:26668357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:18327266 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:18708129 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20150827 MGI PMID:25158856 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17448993 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23230003 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008249 abnormal common lymphocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23435463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20161124 MGI PMID:27303042 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20170314 MGI PMID:25952549 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20181025 MGI PMID:28723571 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21375737 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22155527 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19047372 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008275 failure of endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23213375 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20220714 MGI PMID:35469022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008301 adrenal medulla hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16906226 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008301 adrenal medulla hyperplasia IAGP N RGD:5509061 20180913 MGI PMID:25174395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141127 MGI PMID:18614544 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008329 decreased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008335 decreased gonadotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:24100213 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008341 decreased corticotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:18396135 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22770884 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22770884 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008348 absent gamma-delta T cells IAGP N RGD:5509061 20141003 MGI PMID:22770884 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20200813 MGI PMID:27641500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008372 small malleus IAGP N RGD:5509061 20141003 MGI PMID:17523175 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008376 small malleus manubrium IAGP N RGD:5509061 20141003 MGI PMID:17523175 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20150625 MGI PMID:25552701 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:23378032 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:19906844 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:22155527 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008413 decreased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20220714 MGI PMID:35469022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141218 MGI PMID:24501354 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20240815 MGI PMID:38959316 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20230413 MGI PMID:35379703 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141218 MGI PMID:24501354 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22017987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20180329 MGI PMID:29033352 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:23136411 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21552476 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:23946405 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20141003 MGI PMID:22017987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20180329 MGI PMID:29033352 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20180614 MGI PMID:26025364 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18663224 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17875932 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20170525 MGI PMID:26061883 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20170525 MGI PMID:26061883 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20240613 MGI PMID:38329807 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:23001146 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18316029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18536716 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18693272 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20230511 MGI PMID:33497368 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008492 dorsal root ganglion degeneration IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20201210 MGI PMID:30910745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22138715 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20170706 MGI PMID:26116508 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20231102 MGI PMID:35439434 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20150212 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20150212 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008514 absent retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:17301087 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20150212 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:21552476 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:20562878 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141030 MGI PMID:24700869 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008532 decreased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:18849985 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20151224 MGI PMID:23696872 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:24339869 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20171214 MGI PMID:28319059 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20180329 MGI PMID:29033352 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:23293022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20151224 MGI PMID:24498102 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008559 abnormal interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18725527 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22875805 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20230105 MGI PMID:36217001 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:21724990 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23430111 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20151224 MGI PMID:24498102 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:23136411 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20151224 MGI PMID:24498102 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20151224 MGI PMID:24498102 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:24339869 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008599 increased circulating interleukin-2 level IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:23430111 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:19075395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:23966625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008638 increased circulating interleukin-1 alpha level IAGP N RGD:5509061 20141003 MGI PMID:23293022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:23293022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20151224 MGI PMID:24498102 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:21724990 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:22138715 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:19075395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:23966625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:20123962 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:21724990 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:21724990 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:22138715 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20160811 MGI PMID:25625625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20230105 MGI PMID:36217001 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008728 increased memory B cell number IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008729 decreased memory B cell number IAGP N RGD:5509061 20141003 MGI PMID:20929728 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:17164415 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008732 reduced hair shaft melanin granule number IAGP N RGD:5509061 20190110 MGI PMID:27134165 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:19351896 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:18354198 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008758 abnormal T cell receptor beta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:19110448 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:19279185 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17235291 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18056838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141030 MGI PMID:24523320 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20160505 MGI PMID:21156282 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20190314 MGI PMID:30429376 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20230750 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20407033 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17923094 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23230003 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16782029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008786 abnormal hindgut morphology IAGP N RGD:5509061 20141003 MGI PMID:23893969 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20180301 MGI PMID:28698371 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008797 facial cleft IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22354172 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008806 increased circulating amylase level IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:18316026 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:23455710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:23455710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:18316026 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22659386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008818 abnormal interfrontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19047372 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:23095891 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16782029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18056838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20170525 MGI PMID:26061883 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:15908920 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008829 triphalangia IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008830 abnormal nucleolus morphology IAGP N RGD:5509061 20220324 MGI PMID:35139074 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20141003 MGI PMID:21552476 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17195237 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008847 abnormal suprachiasmatic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18545654 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:23136411 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20141003 MGI PMID:20412777 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20141003 MGI PMID:20412777 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008860 abnormal hair cycle telogen phase IAGP N RGD:5509061 20141003 MGI PMID:20412777 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:21266350 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:22869596 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20210422 MGI PMID:32649882 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18249134 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19729436 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:18056424 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21852535 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20191107 MGI PMID:30224759 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17980593 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20025862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20852630 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22469981 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20191107 MGI PMID:30224759 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008884 abnormal enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22469981 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20025862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22469981 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008901 absent epididymal fat pad IAGP N RGD:5509061 20170119 MGI PMID:27573812 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21896734 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23238710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20170126 MGI PMID:27911893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20210121 MGI PMID:33127760 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008935 decreased mean platelet volume IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22017987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:20346763 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21516099 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21715642 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23444360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23785158 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20180208 MGI PMID:24995979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21482754 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22659386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20170314 MGI PMID:25952549 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:21516099 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20141003 MGI PMID:21516099 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009023 abnormal spinal cord meninges morphology IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009049 abnormal hallux morphology IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:20299358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141030 MGI PMID:24700869 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009052 anal stenosis IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009080 uterus inflammation IAGP N RGD:5509061 20190215 MGI PMID:27018534 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009082 uterus cyst IAGP N RGD:5509061 20190215 MGI PMID:27018534 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18043744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20160728 MGI PMID:25377472 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009094 abnormal endometrial gland morphology IAGP N RGD:5509061 20190215 MGI PMID:27018534 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009105 penis prolapse IAGP N RGD:5509061 20141003 MGI PMID:23817021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:23453624 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009109 decreased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:24332968 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20200416 MGI PMID:32092075 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009132 abnormal white fat cell size IAGP N RGD:5509061 20180208 MGI PMID:24995979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:19679071 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009143 abnormal pancreatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:22964416 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18621715 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22232209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22699621 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23453624 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20150827 MGI PMID:22541435 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20160602 MGI PMID:22863881 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20190516 MGI PMID:28790031 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20191205 MGI PMID:31685994 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20241024 MGI PMID:31048544 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:18621715 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:19028876 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22232209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22699621 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:23453624 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20150827 MGI PMID:22541435 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20160602 MGI PMID:22863881 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20190516 MGI PMID:28790031 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20191205 MGI PMID:31685994 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20241024 MGI PMID:31048544 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22232209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22699621 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20160602 MGI PMID:22863881 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20241024 MGI PMID:31048544 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009156 absent pancreatic acini IAGP N RGD:5509061 20141003 MGI PMID:12185368 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009159 increased pancreatic acinar cell number IAGP N RGD:5509061 20141003 MGI PMID:17980593 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009159 increased pancreatic acinar cell number IAGP N RGD:5509061 20141003 MGI PMID:22146645 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009160 abnormal pancreatic acinar cell zymogen granule morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009164 exocrine pancreas atrophy IAGP N RGD:5509061 20141003 MGI PMID:19943952 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009165 abnormal endocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:14657333 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009167 increased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:24114270 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20200416 MGI PMID:32092075 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009173 absent pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:22964416 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22056672 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22529374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23382704 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:19065048 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:14657333 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:19187772 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009178 absent pancreatic alpha cells IAGP N RGD:5509061 20141003 MGI PMID:14657333 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009179 abnormal pancreatic alpha cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20364121 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009180 increased pancreatic delta cell number IAGP N RGD:5509061 20141003 MGI PMID:23382704 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:18043744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22505453 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:23817021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20170323 MGI PMID:27345403 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20180830 MGI PMID:21795710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20190207 MGI PMID:28292441 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20191212 MGI PMID:27020859 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20220519 MGI PMID:34099734 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22505453 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23817021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20160211 MGI PMID:26058078 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20170323 MGI PMID:27345403 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20180830 MGI PMID:21795710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20190207 MGI PMID:28292441 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220428 MGI PMID:33476744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:23819925 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009246 pale spleen IAGP N RGD:5509061 20151224 MGI PMID:24498102 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009251 enlarged endometrial glands IAGP N RGD:5509061 20190215 MGI PMID:27018534 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141225 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20141003 MGI PMID:23100420 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20150305 MGI PMID:24646999 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009272 decreased guard hair length IAGP N RGD:5509061 20141003 MGI PMID:20412777 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009274 buphthalmos IAGP N RGD:5509061 20150212 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21266350 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20200521 MGI PMID:32142668 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23359070 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20170314 MGI PMID:25952549 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20171207 MGI PMID:26847029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20180405 MGI PMID:29342136 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20190418 MGI PMID:30692594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20201015 MGI PMID:31845480 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18316029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141030 MGI PMID:24374551 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20180208 MGI PMID:24995979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20180208 MGI PMID:24995979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19251594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009317 increased follicular lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20170427 MGI PMID:20499347 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009352 impaired spacing of implantation sites IAGP N RGD:5509061 20170622 MGI PMID:25043182 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009353 twin decidual capsule IAGP N RGD:5509061 20170622 MGI PMID:25043182 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20191128 MGI PMID:23257357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20200310 MGI PMID:27480224 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009385 abnormal dermal pigmentation IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009387 abnormal epidermal pigmentation IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009389 abnormal extracutaneous pigmentation IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009390 abnormal otic pigmentation IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009391 abnormal leptomeninges pigmentation IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:21852535 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:22534068 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:15485899 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20181004 MGI PMID:27907123 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20190314 MGI PMID:30429376 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:17418413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:24132234 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20190314 MGI PMID:30429376 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20181004 MGI PMID:27907123 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20190314 MGI PMID:30429376 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20181004 MGI PMID:27907123 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21828091 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009420 skeletal muscle endomysial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:24132234 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:15314171 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:16791847 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:22063212 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:21807948 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19679071 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20240815 MGI PMID:38959316 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009479 abnormal cecum development IAGP N RGD:5509061 20141003 MGI PMID:22719891 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009497 abnormal intrahepatic bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:19551907 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:23712803 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20201022 MGI PMID:31194862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:21266350 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009511 distended stomach IAGP N RGD:5509061 20141003 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009511 distended stomach IAGP N RGD:5509061 20141003 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009511 distended stomach IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009516 enlarged salivary gland IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20362536 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20141120 MGI PMID:25053428 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20160602 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20160714 MGI PMID:25194568 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009552 urinary bladder obstruction IAGP N RGD:5509061 20141003 MGI PMID:22505453 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009567 mitotic nondisjunction IAGP N RGD:5509061 20170629 MGI PMID:26919979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009571 abnormal right lung accessory lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:19618463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009572 abnormal right lung cranial lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:19618463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009573 abnormal right lung middle lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:19618463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:21248239 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009579 acephaly IAGP N RGD:5509061 20150910 MGI PMID:24895408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20201022 MGI PMID:32343482 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009623 enlarged inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009635 enlarged popliteal lymph nodes IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20200310 MGI PMID:31469588 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220428 MGI PMID:33476744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20141225 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:17164415 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:21498671 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:21505259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009663 abnormal uterine-embryonic axis IAGP N RGD:5509061 20170622 MGI PMID:25043182 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20170622 MGI PMID:25043182 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20160728 MGI PMID:25377472 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19064922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:23293022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18043744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19064922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21376238 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009713 enhanced conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:19270687 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009728 abnormal calcaneum morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009738 enlarged prostate gland anterior lobe IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009744 postaxial polydactyly IAGP N RGD:5509061 20141106 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:20223200 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20170629 MGI PMID:26919979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20180308 MGI PMID:27052165 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20141003 MGI PMID:20404087 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20170629 MGI PMID:26919979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20616797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20161117 MGI PMID:27053202 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:24339869 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20151224 MGI PMID:24498102 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20200409 MGI PMID:31588799 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:20350929 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:23671110 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20230511 MGI PMID:33497368 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20170126 MGI PMID:27911893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20180719 MGI PMID:29781574 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20181122 MGI PMID:25818501 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009784 abnormal melanoblast migration IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009785 abnormal susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20151217 MGI PMID:24489749 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009797 abnormal mismatch repair IAGP N RGD:5509061 20141003 MGI PMID:18264106 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20161013 MGI PMID:26656646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009825 cornea ulcer IAGP N RGD:5509061 20141003 MGI PMID:23293291 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:23410975 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20210506 MGI PMID:31794893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20210520 MGI PMID:24280485 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20220428 MGI PMID:33476744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220428 MGI PMID:33476744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220428 MGI PMID:33476744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20220428 MGI PMID:33476744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009854 impaired gastric peristalsis IAGP N RGD:5509061 20141003 MGI PMID:23535651 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:20570943 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20221124 MGI PMID:31300413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:18483623 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221124 MGI PMID:31300413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20220922 MGI PMID:32169905 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221124 MGI PMID:31300413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009895 decreased palatine bone horizontal plate size IAGP N RGD:5509061 20221124 MGI PMID:31300413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009897 decreased maxillary shelf size IAGP N RGD:5509061 20221006 MGI PMID:23754280 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:16221970 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20190822 MGI PMID:31232685 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20190822 MGI PMID:31232685 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20221124 MGI PMID:31300413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009921 abnormal transitional stage T3 B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009922 increased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:24242374 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009933 abnormal tail hair pigmentation IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009934 abnormal hind foot hair pigmentation IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:23554489 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141218 MGI PMID:24501354 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18832146 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19755104 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21715642 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21943603 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009957 abnormal cerebellum vermis lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009963 abnormal cerebellum hemisphere lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009964 abnormal cerebellum lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:23100420 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009968 abnormal cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15882643 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010013 cerebral cortex pyramidal cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15882643 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010015 abnormal cuticular plate morphology IAGP N RGD:5509061 20171221 MGI PMID:28899994 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20170824 MGI PMID:20733101 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20170824 MGI PMID:20733101 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20103739 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20603627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23028821 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15485899 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20660762 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141030 MGI PMID:24374551 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20191128 MGI PMID:23257357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010031 abnormal cranium size IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010037 ectopic melanocytes IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010038 abnormal placenta physiology IAGP N RGD:5509061 20141003 MGI PMID:22534068 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010039 abnormal trophoblast giant cell proliferation IAGP N RGD:5509061 20170622 MGI PMID:25043182 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141003 MGI PMID:21238928 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141030 MGI PMID:24493648 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20595581 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200310 MGI PMID:31469588 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:19630976 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010072 increased pruritus IAGP N RGD:5509061 20141003 MGI PMID:23263443 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010073 decreased pruritus IAGP N RGD:5509061 20141003 MGI PMID:21139565 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010073 decreased pruritus IAGP N RGD:5509061 20141003 MGI PMID:23263443 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20935052 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20200310 MGI PMID:31469588 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21552476 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23136411 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23946405 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20141016 MGI PMID:24048525 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20160310 MGI PMID:25198863 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20210729 MGI PMID:27464479 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20160310 MGI PMID:25198863 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20180517 MGI PMID:29180569 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010119 abnormal bone mineral density IAGP N RGD:5509061 20220908 MGI PMID:33105483 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010132 decreased DN2 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23230003 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:20407033 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:23077666 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20210520 MGI PMID:24280485 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:22902753 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20150219 MGI PMID:24557836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010156 abnormal small intestinal crypt cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21482754 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010156 abnormal small intestinal crypt cell physiology IAGP N RGD:5509061 20160421 MGI PMID:25690852 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20404087 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21482754 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20160421 MGI PMID:25690852 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20141003 MGI PMID:22469981 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20141003 MGI PMID:23645682 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:21238928 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20200521 MGI PMID:32142668 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010171 abnormal centroacinar cell of Langerhans morphology IAGP N RGD:5509061 20141003 MGI PMID:22146645 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010172 abnormal mammary gland epithelium physiology IAGP N RGD:5509061 20141003 MGI PMID:21266350 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23712803 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24100291 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20150514 MGI PMID:25261485 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20240613 MGI PMID:38329807 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010187 decreased T follicular helper cell number IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010200 enlarged lymphatic vessel IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20160512 MGI PMID:25770585 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:23955076 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141030 MGI PMID:24376268 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20151224 MGI PMID:24498102 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20180920 MGI PMID:29263322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:23966625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21468021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23966625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010224 abnormal heart ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:21145505 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010235 abnormal retina inner limiting membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:23136411 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010236 abnormal retina outer limiting membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:23136411 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21093323 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21685933 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11130972 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010273 increased classified tumor incidence IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010274 increased organ/body region tumor incidence IAGP N RGD:5509061 20150903 MGI PMID:25453902 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22000016 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20160114 MGI PMID:25705882 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010276 increased intraocular melanoma incidence IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23077666 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20160922 MGI PMID:23887970 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20160922 MGI PMID:26704996 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:23077666 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20160922 MGI PMID:23887970 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20160922 MGI PMID:26704996 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20200521 MGI PMID:32142668 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18043744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19251594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20852630 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010281 increased nervous system tumor incidence IAGP N RGD:5509061 20160922 MGI PMID:23887970 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22341446 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010294 increased kidney tumor incidence IAGP N RGD:5509061 20150625 MGI PMID:24732380 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21324922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21482677 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22574128 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010307 abnormal tumor latency IAGP N RGD:5509061 20141003 MGI PMID:23410975 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010307 abnormal tumor latency IAGP N RGD:5509061 20210506 MGI PMID:31794893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:23077666 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20160519 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20210506 MGI PMID:31794893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010312 increased oligodendroglioma incidence IAGP N RGD:5509061 20141003 MGI PMID:23077666 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010312 increased oligodendroglioma incidence IAGP N RGD:5509061 20160922 MGI PMID:23887970 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010312 increased oligodendroglioma incidence IAGP N RGD:5509061 20160922 MGI PMID:26704996 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23023701 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21266350 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22574128 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18043744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20160211 MGI PMID:26058078 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20220519 MGI PMID:34099734 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20180111 MGI PMID:27480224 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010365 increased thymus tumor incidence IAGP N RGD:5509061 20180906 MGI PMID:25565005 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23435463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20141003 MGI PMID:24339869 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20191128 MGI PMID:23257357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010382 abnormal dosage compensation, by inactivation of X chromosome IAGP N RGD:5509061 20141003 MGI PMID:21852535 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010387 abnormal Bergmann glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23100420 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010395 abnormal pharyngeal arch development IAGP N RGD:5509061 20141003 MGI PMID:20596238 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191128 MGI PMID:23257357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20570943 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20210121 MGI PMID:33127760 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010428 abnormal heart right ventricle outflow tract morphology IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010441 total anomalous pulmonary venous connection IAGP N RGD:5509061 20231109 MGI PMID:20071345 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010458 pulmonary trunk hypoplasia IAGP N RGD:5509061 20210121 MGI PMID:33127760 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010466 vascular ring IAGP N RGD:5509061 20141003 MGI PMID:20570943 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010498 abnormal interventricular septum muscular part morphology IAGP N RGD:5509061 20231116 MGI PMID:25315346 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010510 absent P wave IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:21193513 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010522 calcified aorta IAGP N RGD:5509061 20170105 MGI PMID:27812542 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010531 gastrointestinal arteriovenous malformation IAGP N RGD:5509061 20141003 MGI PMID:19805914 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010537 tumor regression IAGP N RGD:5509061 20141003 MGI PMID:17251932 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010537 tumor regression IAGP N RGD:5509061 20141003 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010537 tumor regression IAGP N RGD:5509061 20141003 MGI PMID:23281395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010548 abnormal dorsal mesocardium morphology IAGP N RGD:5509061 20231109 MGI PMID:20071345 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20231109 MGI PMID:36325906 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010584 abnormal conotruncus septation IAGP N RGD:5509061 20160811 MGI PMID:26806701 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20210121 MGI PMID:33127760 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20231102 MGI PMID:35899771 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20160519 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20210506 MGI PMID:31794893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010656 thick myocardium IAGP N RGD:5509061 20141003 MGI PMID:21145505 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010709 absent eye anterior chamber IAGP N RGD:5509061 20201119 MGI PMID:17470285 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010710 absent sclera IAGP N RGD:5509061 20141003 MGI PMID:16203745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010727 increased glioblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21625383 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010741 abnormal melanocyte proliferation IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010741 abnormal melanocyte proliferation IAGP N RGD:5509061 20190110 MGI PMID:27134165 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:18312674 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22606246 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23230003 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23365460 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20161124 MGI PMID:26304963 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20170601 MGI PMID:26544067 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20210722 MGI PMID:32988961 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:20660762 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010784 abnormal forestomach morphology IAGP N RGD:5509061 20141003 MGI PMID:21068065 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010784 abnormal forestomach morphology IAGP N RGD:5509061 20150305 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010796 abnormal intermediate gastric gland morphology IAGP N RGD:5509061 20141003 MGI PMID:15882627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010802 abnormal intestinal enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010809 abnormal club cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23047698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010811 decreased type II pneumocyte number IAGP N RGD:5509061 20180927 MGI PMID:29999500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010828 abnormal bronchioalveolar stem cell morphology IAGP N RGD:5509061 20180927 MGI PMID:29999500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20180920 MGI PMID:27124591 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20170427 MGI PMID:20499347 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20181227 MGI PMID:30204862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:23945236 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20170427 MGI PMID:20499347 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:22792209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20150205 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010896 decreased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:23966625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010898 abnormal pulmonary alveolus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24191021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010899 abnormal pulmonary alveolar system morphology IEA N RGD:5509061 20160218 MGI 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20141003 MGI PMID:23263861 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010906 abnormal lung bud morphology IAGP N RGD:5509061 20141003 MGI PMID:22719891 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010910 bronchiolar epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20548776 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010918 abnormal pulmonary neuroendocrine body morphology IAGP N RGD:5509061 20141003 MGI PMID:23047698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010923 calcified pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:19729436 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010935 increased airway resistance IAGP N RGD:5509061 20141003 MGI PMID:23966625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010945 lung epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20548776 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:21807948 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010951 abnormal lipid oxidation IAGP N RGD:5509061 20141003 MGI PMID:20660762 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:22401858 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20180208 MGI PMID:24995979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20170810 MGI PMID:26356605 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20211209 MGI PMID:33753492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20211209 MGI PMID:33753492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20200310 MGI PMID:31469588 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20170810 MGI PMID:26356605 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20211209 MGI PMID:33753492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:22792209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:19618463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010976 small lung lobe IAGP N RGD:5509061 20141003 MGI PMID:19618463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010979 small ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:20040494 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0010985 abnormal kidney mesenchyme morphology IAGP N RGD:5509061 20150625 MGI PMID:24732380 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011004 abnormal epidermal stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21376238 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19618463 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011044 increased lung elastance IAGP N RGD:5509061 20141003 MGI PMID:23966625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20170803 MGI PMID:28675157 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011082 abnormal gastrointestinal motility IAGP N RGD:5509061 20141003 MGI PMID:23535651 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15314171 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16791847 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17418413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21672919 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22964416 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20150212 MGI PMID:24532689 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170921 MGI PMID:26668357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20230511 MGI PMID:33497368 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12724423 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17360769 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17418413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19064922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20570943 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24327562 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24332968 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20151022 MGI PMID:26324903 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15314171 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17301087 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18331721 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18849985 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19357274 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19644017 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19879843 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19897741 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20299358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21482754 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21927002 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23671110 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24805242 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180712 MGI PMID:27660326 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20201022 MGI PMID:32343482 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20220922 MGI PMID:32169905 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20190829 MGI PMID:30665704 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19906844 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20081196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23971992 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24191021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180517 MGI PMID:29180569 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20210121 MGI PMID:33127760 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19064922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20595581 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141030 MGI PMID:24523320 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20160616 MGI PMID:26952979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16906226 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17418413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20947725 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21505259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23712803 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23410975 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20150910 MGI PMID:24895408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14657333 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15784609 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16267821 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17164415 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17418413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18029401 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19279185 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19415626 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20350929 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:32692983 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20230323 MGI PMID:34767447 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16407399 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17418413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18029401 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20570943 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23410975 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20191003 MGI PMID:30737279 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20221027 MGI PMID:34557486 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21068065 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21807948 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16906226 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19351896 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19357274 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20947725 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23293022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10477299 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17164415 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17344228 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22659386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16015321 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24100213 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20230323 MGI PMID:34767447 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22659386 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011156 abnormal hypodermis fat layer morphology IAGP N RGD:5509061 20151217 MGI PMID:26099023 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20181129 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20180208 MGI PMID:24995979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011169 abnormal white fat cell differentation IAGP N RGD:5509061 20170119 MGI PMID:27573812 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20170119 MGI PMID:27573812 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20141003 MGI PMID:21989989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20150129 MGI PMID:24504341 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10477299 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18171685 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011187 abnormal parietal endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10477299 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011194 abnormal hair follicle physiology IAGP N RGD:5509061 20141003 MGI PMID:20412777 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011195 increased hair follicle apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20412777 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011210 abnormal temporomandibular joint morphology IAGP N RGD:5509061 20141003 MGI PMID:19815519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20141003 MGI PMID:21364967 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011277 decreased tail pigmentation IEA N RGD:5509061 20211118 MGI 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:18056838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011287 increased erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:24121508 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011309 abnormal kidney arterial blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17195237 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011321 abnormal peritubular capillary morphology IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20299358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20220331 MGI PMID:30367465 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:23502960 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:22326220 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:23619366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20220331 MGI PMID:30367465 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011371 decreased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23360989 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011387 absent metanephric mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:20299358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:16267821 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011394 increased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20160929 MGI PMID:25787764 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22401858 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:24262794 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:18327259 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:15987751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15987751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141030 MGI PMID:24700869 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011444 abnormal renal water homeostasis IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:21057506 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:21057506 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011454 abnormal glomerular endothelium fenestra morphology IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011457 abnormal metanephric ureteric bud development IAGP N RGD:5509061 20141003 MGI PMID:20299358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011496 abnormal head size IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011498 abnormal glomerular capsule parietal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15987751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20170622 MGI PMID:25043182 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011585 decreased alkaline phosphatase activity IAGP N RGD:5509061 20141003 MGI PMID:17980593 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011615 submucous cleft palate IAGP N RGD:5509061 20220922 MGI PMID:32169905 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011627 decreased skin pigmentation IEA N RGD:5509061 20211118 MGI 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:21068380 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20210916 MGI PMID:34355730 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:22914740 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20181004 MGI PMID:27907123 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20220428 MGI PMID:33476744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:22914740 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20170126 MGI PMID:27911893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20141003 MGI PMID:22914740 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20170126 MGI PMID:27911893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20170810 MGI PMID:26356605 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011634 abnormal mitochondrial inner membrane morphology IAGP N RGD:5509061 20170810 MGI PMID:26356605 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011642 abnormal bone collagen fibril morphology IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20170126 MGI PMID:27435297 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20210121 MGI PMID:33127760 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20160825 MGI PMID:27466441 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:20299358 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011683 dual inferior vena cava IAGP N RGD:5509061 20231109 MGI PMID:20071345 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20404087 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20571512 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:21930934 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:23281395 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20171109 MGI PMID:26774483 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20220127 MGI PMID:17967868 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011705 absent fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:23975099 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011706 abnormal fibroblast migration IAGP N RGD:5509061 20141003 MGI PMID:20231695 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20170223 MGI PMID:20231695 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20141003 MGI PMID:23785158 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011730 increased myelin sheath thickness IAGP N RGD:5509061 20141030 MGI PMID:24493648 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20141030 MGI PMID:24493648 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20161013 MGI PMID:26656646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:23671110 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011747 myelofibrosis IAGP N RGD:5509061 20141003 MGI PMID:20010698 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011748 intestinal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19217431 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20200409 MGI PMID:31588799 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011771 abnormal genital tubercle morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011775 rectal atresia IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011786 rectourethral fistula IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20231116 MGI PMID:25315346 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24332968 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011856 abnormal glomerular filtration barrier function IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011873 enlarged uterine horn IAGP N RGD:5509061 20190215 MGI PMID:27018534 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011901 abnormal hematopoietic stem cell proliferation IAGP N RGD:5509061 20151217 MGI PMID:24440599 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22606246 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22699452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20151217 MGI PMID:24440599 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011903 decreased hematopoietic stem cell proliferation IAGP N RGD:5509061 20210722 MGI PMID:32988961 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011932 abnormal endocrine pancreas development IAGP N RGD:5509061 20141003 MGI PMID:24114270 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:20103739 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:21076408 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011939 increased food intake IAGP N RGD:5509061 20141030 MGI PMID:24374551 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141030 MGI PMID:24374551 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:21283519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20170216 MGI PMID:26935106 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23408898 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20180712 MGI PMID:27660326 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20191212 MGI PMID:29961578 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210218 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0011994 increased nerve conduction velocity IAGP N RGD:5509061 20141030 MGI PMID:24493648 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012001 abnormal touch escape response IAGP N RGD:5509061 20190509 MGI PMID:30305456 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012021 abnormal melanocyte number IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20160128 MGI PMID:26113083 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20170126 MGI PMID:27911893 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20190110 MGI PMID:27134165 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012049 increased susceptilbility to retina ischemic injury IAGP N RGD:5509061 20141016 MGI PMID:24048525 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012050 decreased susceptilbility to retina ischemic injury IAGP N RGD:5509061 20141016 MGI PMID:24048525 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012065 increased astrocyte number IAGP N RGD:5509061 20141003 MGI PMID:23893969 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012065 increased astrocyte number IAGP N RGD:5509061 20141016 MGI PMID:24048525 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012066 decreased astrocyte number IAGP N RGD:5509061 20141016 MGI PMID:24048525 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012075 impaired mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:23712803 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:18029401 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012084 truncated foregut IAGP N RGD:5509061 20221006 MGI PMID:36046192 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:22190459 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:16267821 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:17537797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012100 absent spongiotrophoblast IAGP N RGD:5509061 20141003 MGI PMID:21852535 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20141003 MGI PMID:16267821 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012133 absent midbrain-hindbrain boundary IAGP N RGD:5509061 20141003 MGI PMID:22190459 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:19093031 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012141 absent hindbrain IAGP N RGD:5509061 20141003 MGI PMID:22190459 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20230413 MGI PMID:32440726 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20230413 MGI PMID:32440726 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012174 flat head IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012176 abnormal head development IAGP N RGD:5509061 20171109 MGI PMID:15107405 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012179 abnormal splanchnic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16720880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012183 decreased paraxial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:22995555 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012200 increased endothelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22753193 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012201 decreased endothelial cell proliferation IAGP N RGD:5509061 20170314 MGI PMID:23911327 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012204 abnormal neuronal stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23893969 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012204 abnormal neuronal stem cell physiology IAGP N RGD:5509061 20200130 MGI PMID:31112699 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012206 increased neuronal stem cell self-renewal IAGP N RGD:5509061 20141003 MGI PMID:23893969 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012224 abnormal sterol level IAGP N RGD:5509061 20210701 MGI PMID:33524375 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20141218 MGI PMID:24501354 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20240815 MGI PMID:38959316 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012362 increased large unstained cell number IAGP N RGD:5509061 20141003 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012416 decreased gland tumor incidence IAGP N RGD:5509061 20241024 MGI PMID:31048544 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11130972 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16015321 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17456738 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19064922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19808965 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20947725 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21324922 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21441929 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21458673 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21493594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012490 abnormal cochlear VIII nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012492 pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012552 lactic acidosis IAGP N RGD:5509061 20200310 MGI PMID:31469588 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012556 increased cell death IAGP N RGD:5509061 20170608 MGI PMID:27974209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012556 increased cell death IAGP N RGD:5509061 20170629 MGI PMID:26919979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20180920 MGI PMID:19630976 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012674 tomacula IAGP N RGD:5509061 20141030 MGI PMID:24493648 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20230309 MGI PMID:23872235 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012709 delayed caudal neuropore closure IAGP N RGD:5509061 20151001 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012745 abnormal neural crest cell physiology IAGP N RGD:5509061 20231102 MGI PMID:35899771 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012747 abnormal cardiac neural crest cell morphology IAGP N RGD:5509061 20171109 MGI PMID:26545946 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012748 increased cardiac neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:17344228 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012749 decreased cardiac neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:15789410 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012749 decreased cardiac neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:17344228 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012749 decreased cardiac neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:19541608 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012751 impaired cardiac neural crest cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17344228 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:15789410 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20160811 MGI PMID:26806701 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20231102 MGI PMID:35899771 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012754 abnormal cranial neural crest cell morphology IAGP N RGD:5509061 20221027 MGI PMID:34184034 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012755 decreased cranial neural crest cell number IAGP N RGD:5509061 20230309 MGI PMID:35593225 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012756 impaired cranial neural crest cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19541608 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012756 impaired cranial neural crest cell differentiation IAGP N RGD:5509061 20210121 MGI PMID:33127760 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012757 abnormal cranial neural crest cell migration IAGP N RGD:5509061 20210121 MGI PMID:33127760 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012760 decreased cranial neural crest cell proliferation IAGP N RGD:5509061 20221027 MGI PMID:34184034 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012760 decreased cranial neural crest cell proliferation IAGP N RGD:5509061 20230309 MGI PMID:23872235 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012761 increased cranial neural crest cell apoptosis IAGP N RGD:5509061 20200917 MGI PMID:31733190 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012761 increased cranial neural crest cell apoptosis IAGP N RGD:5509061 20230309 MGI PMID:23872235 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012761 increased cranial neural crest cell apoptosis IAGP N RGD:5509061 20230309 MGI PMID:35593225 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0012785 decreased rhombomere 1 size IAGP N RGD:5509061 20141003 MGI PMID:17537797 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013006 abnormal enteric neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:18693272 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013139 moribund IAGP N RGD:5509061 20160623 MGI PMID:25082229 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013164 abnormal forelimb bud morphology IAGP N RGD:5509061 20231130 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013180 truncated tail bud IAGP N RGD:5509061 20141003 MGI PMID:22991437 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20160811 MGI PMID:25625625 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013199 increased head mesenchyme apoptosis IAGP N RGD:5509061 20230309 MGI PMID:23872235 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20150723 MGI PMID:25451152 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20141003 MGI PMID:22232209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20141120 MGI PMID:23453624 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20150827 MGI PMID:22541435 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20160310 MGI PMID:17980593 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20241024 MGI PMID:31048544 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013225 abnormal third pharyngeal pouch morphology IAGP N RGD:5509061 20141120 MGI PMID:25053428 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20160721 MGI PMID:26999603 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:21828091 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211209 MGI PMID:33753492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:24332968 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20191128 MGI PMID:23257357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20200416 MGI PMID:32092075 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013285 abnormal renal filtration IAGP N RGD:5509061 20240829 MGI PMID:38797325 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013289 abnormal mitotic cytokinesis IAGP N RGD:5509061 20180301 MGI PMID:28698371 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20150219 MGI PMID:24557836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20210729 MGI PMID:31241981 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013307 increased adrenal gland weight IAGP N RGD:5509061 20141120 MGI PMID:19897935 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013328 visceromegaly IAGP N RGD:5509061 20180920 MGI PMID:29899452 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013335 hepatic peliosis IAGP N RGD:5509061 20141204 MGI PMID:15784609 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013374 increased sebaceous gland tumor incidence IAGP N RGD:5509061 20160602 MGI PMID:22863881 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013400 abnormal endometrial gland development IAGP N RGD:5509061 20190215 MGI PMID:27018534 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013464 decreased conjunctiva goblet cell number IAGP N RGD:5509061 20150212 MGI PMID:23293291 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013465 abnormal conjunctiva goblet cell differentiation IAGP N RGD:5509061 20150212 MGI PMID:23293291 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013481 abnormal ileum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20160310 MGI PMID:22902753 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013482 abnormal duodenum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20150319 MGI PMID:18536716 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013483 abnormal jejunum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20150319 MGI PMID:18536716 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013485 increased Paneth cell number IAGP N RGD:5509061 20150312 MGI PMID:20025862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013488 increased keratoacanthoma incidence IAGP N RGD:5509061 20150212 MGI PMID:17456738 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20171109 MGI PMID:26774483 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013600 testis degeneration IAGP N RGD:5509061 20150312 MGI PMID:23408915 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013600 testis degeneration IAGP N RGD:5509061 20160519 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20220324 MGI PMID:29293683 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013623 increased femur compact bone thickness IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20181227 MGI PMID:30204862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20170427 MGI PMID:20499347 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013638 decreased femur stiffness IAGP N RGD:5509061 20220922 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013640 increased bone stiffness IAGP N RGD:5509061 20181227 MGI PMID:30204862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013660 abnormal bone marrow hematopoietic cell morphology IAGP N RGD:5509061 20190418 MGI PMID:30692594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20161124 MGI PMID:26304963 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013696 increased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013696 increased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20190418 MGI PMID:30692594 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013701 abnormal mature B cell number IAGP N RGD:5509061 20170525 MGI PMID:26061883 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013744 abnormal conjunctival sac morphology IAGP N RGD:5509061 20150416 MGI PMID:23293291 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:18372904 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013805 myeloid metaplasia IAGP N RGD:5509061 20171102 MGI PMID:26438359 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013905 preputial gland inflammation IAGP N RGD:5509061 20180322 MGI PMID:29415061 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013940 abnormal plasmablast number IAGP N RGD:5509061 20170921 MGI PMID:26668357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013940 abnormal plasmablast number IAGP N RGD:5509061 20210826 MGI PMID:33336366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0013958 decreased small intestine length IAGP N RGD:5509061 20160310 MGI PMID:19273838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014049 increased T cell acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20180906 MGI PMID:25565005 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20181025 MGI PMID:28723571 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20210916 MGI PMID:34355730 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014057 abnormal mammary gland stroma morphology IAGP N RGD:5509061 20201022 MGI PMID:31194862 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014062 nervous system inclusion bodies IAGP N RGD:5509061 20180614 MGI PMID:26025364 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014076 absent Paneth cells IAGP N RGD:5509061 20160310 MGI PMID:17980593 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014076 absent Paneth cells IAGP N RGD:5509061 20160310 MGI PMID:22354172 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014077 ectopic Paneth cells IAGP N RGD:5509061 20160310 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014077 ectopic Paneth cells IAGP N RGD:5509061 20160310 MGI PMID:22902753 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014077 ectopic Paneth cells IAGP N RGD:5509061 20160421 MGI PMID:25690852 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014078 small intestinal villus atrophy IAGP N RGD:5509061 20160310 MGI PMID:19884656 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014080 fused small intestinal villi IAGP N RGD:5509061 20160310 MGI PMID:24557836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20160310 MGI PMID:19273838 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014083 blunted small intestinal villi IAGP N RGD:5509061 20160310 MGI PMID:24557836 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:17505543 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014106 delayed chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014126 increased mammary gland apoptosis IAGP N RGD:5509061 20160317 MGI PMID:21266350 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014127 increased thymoma incidence IAGP N RGD:5509061 20180906 MGI PMID:25565005 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20171109 MGI PMID:26774483 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014141 abnormal mesoderm morphology IAGP N RGD:5509061 20171109 MGI PMID:26774483 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20200310 MGI PMID:31469588 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20180208 MGI PMID:24995979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20170810 MGI PMID:26356605 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014174 decreased fatty acid beta-oxidation IAGP N RGD:5509061 20160421 MGI PMID:23355744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014179 abnormal blood-retina barrier function IAGP N RGD:5509061 20160526 MGI PMID:23136411 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:19965762 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014186 epididymis hypertrophy IAGP N RGD:5509061 20160526 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014187 spermatocele IAGP N RGD:5509061 20160526 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014188 epididymis fibrosis IAGP N RGD:5509061 20160526 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014192 increased epididymal cell proliferation IAGP N RGD:5509061 20160526 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014194 increased epididymal epithelium cell proliferation IAGP N RGD:5509061 20160526 MGI PMID:25759215 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:18043744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:21266350 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:21339646 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:22510880 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014242 abnormal ribosome biogenesis IAGP N RGD:5509061 20230615 MGI PMID:24062412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014273 abnormal skin vasculature morphology IAGP N RGD:5509061 20230810 MGI PMID:20407033 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:25034710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:17164415 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:18423204 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:17164415 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014331 abnormal Purkinje cell mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:23041622 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014347 increased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:18490492 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014348 decreased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:21795747 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014368 enhanced long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:24501354 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014436 decreased interferon level IAGP N RGD:5509061 20240502 MGI PMID:32814047 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014440 increased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:24374551 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0014441 decreased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:23028821 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220908 MGI PMID:33105483 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:22792209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20170309 MGI PMID:26333933 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20170413 MGI PMID:26896819 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20220519 MGI PMID:29396429 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020067 increased neocortex size IAGP N RGD:5509061 20180329 MGI PMID:29033352 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20180614 MGI PMID:29621230 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020138 delayed bone mineralization IAGP N RGD:5509061 20180517 MGI PMID:29180569 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020154 impaired humoral immune response IAGP N RGD:5509061 20210826 MGI PMID:33336366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020154 impaired humoral immune response IAGP N RGD:5509061 20240627 MGI PMID:38438357 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020186 abnormal susceptibility to bacterial infection IAGP N RGD:5509061 20150514 MGI PMID:25261485 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020327 abnormal capillary branching pattern IAGP N RGD:5509061 20160714 MGI PMID:17646578 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020329 decreased capillary density IAGP N RGD:5509061 20160714 MGI PMID:20944627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020329 decreased capillary density IAGP N RGD:5509061 20160714 MGI PMID:21852535 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020329 decreased capillary density IAGP N RGD:5509061 20241107 MGI PMID:35477278 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20161013 MGI PMID:19788412 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20170608 MGI PMID:27974209 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20200514 MGI PMID:31833196 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020367 increased heart iron level IAGP N RGD:5509061 20161020 MGI PMID:18316026 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020367 increased heart iron level IAGP N RGD:5509061 20181115 MGI PMID:29257745 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020369 increased intestinal iron level IAGP N RGD:5509061 20161020 MGI PMID:23455710 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020383 decreased kidney epithelial cell primary cilium length IAGP N RGD:5509061 20161013 MGI PMID:24700869 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20161124 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020410 increased liposarcoma incidence IAGP N RGD:5509061 20180111 MGI PMID:27573812 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20170202 MGI PMID:23785158 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20220224 MGI PMID:29514850 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020416 decreased fibroblast chemotaxis IAGP N RGD:5509061 20170223 MGI PMID:20231695 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020431 decreased platelet alpha-granule number IAGP N RGD:5509061 20170720 MGI PMID:25947942 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020450 abnormal sperm progressive motility IAGP N RGD:5509061 20220714 MGI PMID:35469022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:18545654 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20180830 MGI PMID:29809135 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20240815 MGI PMID:38959316 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020521 browned white adipose tissue morphology IAGP N RGD:5509061 20180208 MGI PMID:24995979 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20180125 MGI PMID:24374551 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20210916 MGI PMID:34355730 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20240815 MGI PMID:38959316 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20230105 MGI PMID:36217001 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:30142928 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0021023 increased adipose tissue noradrenaline turnover IAGP N RGD:5509061 20220106 MGI PMID:24374551 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0021091 abnormal dorsal interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:15901662 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0021103 abnormal ventral interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:16525473 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:17470285 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:19850870 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0021202 abnormal palatopharyngeus muscle morphology IAGP N RGD:5509061 20221103 MGI PMID:34557486 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0021204 abnormal superior pharyngeal constrictor muscle morphology IAGP N RGD:5509061 20221103 MGI PMID:34557486 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030025 giant platelets IAGP N RGD:5509061 20170803 MGI PMID:22878500 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030047 flat forehead IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030066 short face IAGP N RGD:5509061 20171207 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030091 macrodontia IAGP N RGD:5509061 20171005 MGI PMID:22473653 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030118 rhinosinusitis IAGP N RGD:5509061 20210211 MGI PMID:19675306 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030122 temporal bone squamous part hypoplasia IAGP N RGD:5509061 20230928 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030224 abnormal soft palate muscle morphology IAGP N RGD:5509061 20221027 MGI PMID:34557486 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030245 round head IAGP N RGD:5509061 20171019 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030249 small frontonasal prominence IAGP N RGD:5509061 20221006 MGI PMID:23754280 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030258 small mandibular condyloid process IAGP N RGD:5509061 20171019 MGI PMID:19815519 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030278 thick neurocranium IAGP N RGD:5509061 20171102 MGI PMID:20499347 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030283 small mandibular coronoid process IAGP N RGD:5509061 20171102 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030287 enlarged occipital bone IAGP N RGD:5509061 20171102 MGI PMID:25453902 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030292 abnormal tensor veli palatini muscle morphology IAGP N RGD:5509061 20221103 MGI PMID:34557486 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030294 abnormal levator veli palatini muscle morphology IAGP N RGD:5509061 20221103 MGI PMID:34557486 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030313 abnormal face development IAGP N RGD:5509061 20171109 MGI PMID:15107405 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171207 MGI PMID:19047372 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030367 premature metopic suture closure IAGP N RGD:5509061 20171207 MGI PMID:19047372 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030372 enlarged Meckel's cartilage IAGP N RGD:5509061 20171207 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030603 increased sperm number IAGP N RGD:5509061 20220714 MGI PMID:35469022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030835 abnormal ankle joint morphology IAGP N RGD:5509061 20181025 MGI PMID:20215352 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030911 increased melanoblast apoptosis IAGP N RGD:5509061 20190411 MGI PMID:29781574 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20210916 MGI PMID:34355730 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:20404087 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030949 abnormal Golgi vesicle transport IAGP N RGD:5509061 20190725 MGI PMID:29180569 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030952 abnormal Golgi stack morphology IAGP N RGD:5509061 20190725 MGI PMID:29180569 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030984 increased circulating osteocalcin level IAGP N RGD:5509061 20191219 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030985 decreased circulating osteocalcin level IAGP N RGD:5509061 20191219 MGI PMID:21557308 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030987 spinal cord inflammation IAGP N RGD:5509061 20191128 MGI PMID:18641296 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030991 optic nerve inflammation IAGP N RGD:5509061 20191128 MGI PMID:18641296 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20191128 MGI PMID:19415626 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031015 abnormal granulosa cell apoptosis IAGP N RGD:5509061 20200130 MGI PMID:20005806 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20230105 MGI PMID:36217001 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031040 increased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20240502 MGI PMID:32814047 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031058 hepatosplenomegaly IAGP N RGD:5509061 20200618 MGI PMID:28846072 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031074 increased circulating type I collagen C-terminal telopeptide level IAGP N RGD:5509061 20200618 MGI PMID:24497849 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031110 meningitis IAGP N RGD:5509061 20200910 MGI PMID:24046360 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:16977322 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21779369 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:23355744 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031154 intestinal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:17496203 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031204 hindlimb paresis IAGP N RGD:5509061 20210218 MGI PMID:20693987 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031204 hindlimb paresis IAGP N RGD:5509061 20210218 MGI PMID:22685206 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031213 increased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031216 decreased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20240620 MGI PMID:35680100 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031304 impaired behavioral response to methamphetamine IAGP N RGD:5509061 20211028 MGI PMID:24587241 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:24132234 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031365 prostate gland ventral lobe hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:23817021 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:20944627 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20230511 MGI PMID:33497368 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:18316029 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031426 increased sperm motility IAGP N RGD:5509061 20220714 MGI PMID:35469022 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221124 MGI PMID:31300413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031445 midline cleft upper lip IAGP N RGD:5509061 20231102 MGI PMID:37075751 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:22219353 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031454 decreased cranial neural crest cell apoptosis IAGP N RGD:5509061 20221110 MGI PMID:34184034 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031458 absent palate bones IAGP N RGD:5509061 20221124 MGI PMID:32169905 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:34557486 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031464 abnormal spontaneous fetal mouth movement IAGP N RGD:5509061 20230302 MGI PMID:31300413 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031472 abnormal female germ cell apoptosis IAGP N RGD:5509061 20230615 MGI PMID:20005806 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031500 increased cornea size IAGP N RGD:5509061 20230810 MGI PMID:25202984 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031509 decreased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:36073366 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031590 abnormal epicardium development IAGP N RGD:5509061 20240229 MGI PMID:19369973 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031590 abnormal epicardium development IAGP N RGD:5509061 20240229 MGI PMID:22926762 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:16791847 2303939 Gt(ROSA)26Sor gene trap ROSA 26, Philippe Soriano gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:21091282 2304167 Tgfbr3l transforming growth factor, beta receptor III-like gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220106 MGI PMID:34910520 2304167 Tgfbr3l transforming growth factor, beta receptor III-like gene MP:0001934 increased litter size IAGP N RGD:5509061 20220106 MGI PMID:34910520 2304167 Tgfbr3l transforming growth factor, beta receptor III-like gene MP:0002681 increased corpora lutea number IAGP N RGD:5509061 20220106 MGI PMID:34910520 2304167 Tgfbr3l transforming growth factor, beta receptor III-like gene MP:0004855 increased ovary weight IAGP N RGD:5509061 20220106 MGI PMID:34910520 2304167 Tgfbr3l transforming growth factor, beta receptor III-like gene MP:0005131 increased follicle stimulating hormone level IAGP N RGD:5509061 20220106 MGI PMID:34910520 2304167 Tgfbr3l transforming growth factor, beta receptor III-like gene MP:0011128 increased tertiary ovarian follicle number IAGP N RGD:5509061 20220106 MGI PMID:34910520 2304167 Tgfbr3l transforming growth factor, beta receptor III-like gene MP:0020152 abnormal oocyte number IAGP N RGD:5509061 20220106 MGI PMID:34910520 2306382 Yy2 Yy2 transcription factor gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 2306382 Yy2 Yy2 transcription factor gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 2306382 Yy2 Yy2 transcription factor gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 2306382 Yy2 Yy2 transcription factor gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 2306601 Tmem95 transmembrane protein 95 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20201022 MGI PMID:32484434 2306601 Tmem95 transmembrane protein 95 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220811 MGI PMID:34982145 2306601 Tmem95 transmembrane protein 95 gene MP:0001925 male infertility IAGP N RGD:5509061 20200716 MGI PMID:32393636 2306601 Tmem95 transmembrane protein 95 gene MP:0001925 male infertility IAGP N RGD:5509061 20201022 MGI PMID:32484434 2306601 Tmem95 transmembrane protein 95 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220811 MGI PMID:34982145 2306601 Tmem95 transmembrane protein 95 gene MP:0031010 failure of sperm-egg fusion IAGP N RGD:5509061 20200716 MGI PMID:32393636 2306601 Tmem95 transmembrane protein 95 gene MP:0031010 failure of sperm-egg fusion IAGP N RGD:5509061 20201022 MGI PMID:32484434 2306601 Tmem95 transmembrane protein 95 gene MP:0031010 failure of sperm-egg fusion IAGP N RGD:5509061 20220811 MGI PMID:34982145 2306857 Topaz1 testis and ovary specific PAZ domain containing 1 gene MP:0001147 small testis IAGP N RGD:5509061 20160107 MGI PMID:26358182 2306857 Topaz1 testis and ovary specific PAZ domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20160107 MGI PMID:26358182 2306857 Topaz1 testis and ovary specific PAZ domain containing 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20160107 MGI PMID:26358182 2306857 Topaz1 testis and ovary specific PAZ domain containing 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20160107 MGI PMID:26358182 2306857 Topaz1 testis and ovary specific PAZ domain containing 1 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20160107 MGI PMID:26358182 2306857 Topaz1 testis and ovary specific PAZ domain containing 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20160107 MGI PMID:26358182 2306857 Topaz1 testis and ovary specific PAZ domain containing 1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20160107 MGI PMID:26358182 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0001314 cornea opacity IEA N RGD:5509061 20240523 MGI 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0002750 exophthalmos IEA N RGD:5509061 20240523 MGI 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0005287 narrow eye opening IEA N RGD:5509061 20240523 MGI 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20240523 MGI 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0012297 hyperactivity elicited by feed restriction IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0013138 thin body IAGP N RGD:5509061 20240704 MGI PMID:35412887 2306863 Alkal2 ALK and LTK ligand 2 gene MP:0020521 browned white adipose tissue morphology IAGP N RGD:5509061 20240704 MGI PMID:35412887 2307654 Pramel47 PRAME like 47 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240613 MGI PMID:38786026 2308010 Jmjd7 jumonji domain containing 7 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 2308010 Jmjd7 jumonji domain containing 7 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 2308098 Mndal myeloid nuclear differentiation antigen like gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 2308098 Mndal myeloid nuclear differentiation antigen like gene MP:0001406 abnormal gait IEA N RGD:5509061 20230601 MGI 2308098 Mndal myeloid nuclear differentiation antigen like gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230119 MGI 2308098 Mndal myeloid nuclear differentiation antigen like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 2308226 Cbln1os cerebellin 1 precursor protein opposite strand gene MP:0000852 small cerebellum IAGP N RGD:5509061 20211125 MGI PMID:33762741 2308226 Cbln1os cerebellin 1 precursor protein opposite strand gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20211125 MGI PMID:33762741 2308226 Cbln1os cerebellin 1 precursor protein opposite strand gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20211125 MGI PMID:33762741 2308226 Cbln1os cerebellin 1 precursor protein opposite strand gene MP:0001405 impaired coordination IAGP N RGD:5509061 20211125 MGI PMID:33762741 2308226 Cbln1os cerebellin 1 precursor protein opposite strand gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20211125 MGI PMID:33762741 2308226 Cbln1os cerebellin 1 precursor protein opposite strand gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20211125 MGI PMID:33762741 2308226 Cbln1os cerebellin 1 precursor protein opposite strand gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20211125 MGI PMID:33762741 2308226 Cbln1os cerebellin 1 precursor protein opposite strand gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20211125 MGI PMID:33762741 2308226 Cbln1os cerebellin 1 precursor protein opposite strand gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20211125 MGI PMID:33762741 2308226 Cbln1os cerebellin 1 precursor protein opposite strand gene MP:0012525 abnormal rhombic lip morphology IAGP N RGD:5509061 20211125 MGI PMID:33762741 2308226 Cbln1os cerebellin 1 precursor protein opposite strand gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:33762741 2308226 Cbln1os cerebellin 1 precursor protein opposite strand gene MP:0014558 decreased cortical ventricular zone thickness IAGP N RGD:5509061 20241031 MGI PMID:33762741 2308242 Pakap paralemmin A kinase anchor protein gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20240418 MGI PMID:34831084 2308242 Pakap paralemmin A kinase anchor protein gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20240418 MGI PMID:34831084 2308242 Pakap paralemmin A kinase anchor protein gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20240418 MGI PMID:34831084 2308242 Pakap paralemmin A kinase anchor protein gene MP:0031217 increased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20240418 MGI PMID:34831084 2308384 Gfy golgi-associated olfactory signaling regulator gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20200310 MGI PMID:23926254 2308384 Gfy golgi-associated olfactory signaling regulator gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:23926254 2308384 Gfy golgi-associated olfactory signaling regulator gene MP:0011281 abnormal olfactory epithelium cilium morphology IAGP N RGD:5509061 20200310 MGI PMID:23926254 2308384 Gfy golgi-associated olfactory signaling regulator gene MP:0012020 abnormal olfactory epithelium physiology IAGP N RGD:5509061 20200310 MGI PMID:23926254 2308427 Ccl27al C-C motif chemokine ligand 27A like gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20240613 MGI PMID:35663027 2308427 Ccl27al C-C motif chemokine ligand 27A like gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20240613 MGI PMID:35663027 2308427 Ccl27al C-C motif chemokine ligand 27A like gene MP:0009080 uterus inflammation IAGP N RGD:5509061 20240613 MGI PMID:35663027 2308427 Ccl27al C-C motif chemokine ligand 27A like gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20240613 MGI PMID:35663027 2308427 Ccl27al C-C motif chemokine ligand 27A like gene MP:0012572 increased susceptibility to chemically induced skin inflammation IAGP N RGD:5509061 20240613 MGI PMID:35663027 2308427 Ccl27al C-C motif chemokine ligand 27A like gene MP:0020212 impaired leukocyte migration IAGP N RGD:5509061 20240613 MGI PMID:35663027 2308439 Sirpd signal regulatory protein delta gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 2308439 Sirpd signal regulatory protein delta gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230601 MGI 2308490 Mthfsl 5, 10-methenyltetrahydrofolate synthetase-like gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 2308490 Mthfsl 5, 10-methenyltetrahydrofolate synthetase-like gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 2308490 Mthfsl 5, 10-methenyltetrahydrofolate synthetase-like gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160421 MGI 2310697 Ctag2 cancer/testis antigen 2 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20201224 MGI PMID:32493902 2311160 Pmis2 PMIS2 transmembrane protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22621904 2311160 Pmis2 PMIS2 transmembrane protein gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:22621904 2311160 Pmis2 PMIS2 transmembrane protein gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:22621904 2311160 Pmis2 PMIS2 transmembrane protein gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20220303 MGI PMID:22621904 2311160 Pmis2 PMIS2 transmembrane protein gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220303 MGI PMID:22621904 2311273 Ifi208 interferon activated gene 208 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 2311273 Ifi208 interferon activated gene 208 gene MP:0000692 small spleen IEA N RGD:5509061 20210128 MGI 2311273 Ifi208 interferon activated gene 208 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 2311273 Ifi208 interferon activated gene 208 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 2311273 Ifi208 interferon activated gene 208 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 2311273 Ifi208 interferon activated gene 208 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20220331 MGI PMID:35171680 2311276 Lratd2 LRAT domain containing 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 2311276 Lratd2 LRAT domain containing 1 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20210520 MGI 2311276 Lratd2 LRAT domain containing 1 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210520 MGI 2311276 Lratd2 LRAT domain containing 1 gene MP:0008206 increased B-2 B cell number IEA N RGD:5509061 20210520 MGI 2311276 Lratd2 LRAT domain containing 1 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20210128 MGI 2311278 Fam246a family with sequence similarity 246 member A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240321 MGI PMID:32668405 2311283 Pom121l2 POM121 transmembrane nucleoporin like 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 2311283 Pom121l2 POM121 transmembrane nucleoporin like 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 2311287 Ccdc166 coiled-coil domain containing 166 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220811 MGI 2311287 Ccdc166 coiled-coil domain containing 166 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210826 MGI 2311291 Pgbd1 piggyBac transposable element derived 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20200402 MGI 2311291 Pgbd1 piggyBac transposable element derived 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200402 MGI 2311291 Pgbd1 piggyBac transposable element derived 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20200402 MGI 2311291 Pgbd1 piggyBac transposable element derived 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20200402 MGI 2311291 Pgbd1 piggyBac transposable element derived 1 gene MP:0001147 small testis IEA N RGD:5509061 20200402 MGI 2311291 Pgbd1 piggyBac transposable element derived 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20181227 MGI 2311291 Pgbd1 piggyBac transposable element derived 1 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20200402 MGI 2311291 Pgbd1 piggyBac transposable element derived 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20200402 MGI 2311291 Pgbd1 piggyBac transposable element derived 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200402 MGI 2311291 Pgbd1 piggyBac transposable element derived 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20200402 MGI 2311291 Pgbd1 piggyBac transposable element derived 1 gene MP:0002637 small uterus IEA N RGD:5509061 20200402 MGI 2311291 Pgbd1 piggyBac transposable element derived 1 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20200402 MGI 2311291 Pgbd1 piggyBac transposable element derived 1 gene MP:0004958 enlarged prostate gland IEA N RGD:5509061 20200402 MGI 2311291 Pgbd1 piggyBac transposable element derived 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20200402 MGI 2311830 Parp10 poly (ADP-ribose) polymerase family, member 10 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19625254 2311830 Parp10 poly (ADP-ribose) polymerase family, member 10 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:19625254 2312710 Gon4l gon-4 like gene MP:0000621 increased salivary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23608756 2312710 Gon4l gon-4 like gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:20530203 2312710 Gon4l gon-4 like gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20530203 2312710 Gon4l gon-4 like gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:20530203 2312710 Gon4l gon-4 like gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20530203 2312710 Gon4l gon-4 like gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20530203 2312710 Gon4l gon-4 like gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:20530203 2312710 Gon4l gon-4 like gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20530203 2312710 Gon4l gon-4 like gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20530203 2312710 Gon4l gon-4 like gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:20530203 2312710 Gon4l gon-4 like gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20530203 2312710 Gon4l gon-4 like gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:20530203 2312710 Gon4l gon-4 like gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:20530203 2313371 Adam20 a disintegrin and metallopeptidase domain 20 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210128 MGI 2313371 Adam20 a disintegrin and metallopeptidase domain 20 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 2314059 Mir582 microRNA 582 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20240912 MGI PMID:35685988 2314059 Mir582 microRNA 582 gene MP:0004979 abnormal neuronal precursor cell number IAGP N RGD:5509061 20240912 MGI PMID:35685988 2314059 Mir582 microRNA 582 gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20240912 MGI PMID:35685988 2314059 Mir582 microRNA 582 gene MP:0012207 decreased neuronal stem cell self-renewal IAGP N RGD:5509061 20240912 MGI PMID:35685988 2314060 Mir511 microRNA 511 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20240328 MGI PMID:35011620 2314060 Mir511 microRNA 511 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20240328 MGI PMID:35011620 2314075 Mir92b microRNA 92b gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20240404 MGI PMID:37985354 2314075 Mir92b microRNA 92b gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20240404 MGI PMID:37985354 2314075 Mir92b microRNA 92b gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20240404 MGI PMID:37985354 2314075 Mir92b microRNA 92b gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20240404 MGI PMID:37985354 2314075 Mir92b microRNA 92b gene MP:0010238 increased skeletal muscle weight IAGP N RGD:5509061 20240404 MGI PMID:37985354 2314075 Mir92b microRNA 92b gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20240404 MGI PMID:37985354 2314075 Mir92b microRNA 92b gene MP:0012107 enhanced exercise endurance IAGP N RGD:5509061 20240404 MGI PMID:37985354 2314075 Mir92b microRNA 92b gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20240404 MGI PMID:37985354 2314107 Mir208b microRNA 208b gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19922871 2314107 Mir208b microRNA 208b gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:19922871 2314108 Mir193b microRNA 193b gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 2314108 Mir193b microRNA 193b gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20160317 MGI PMID:25236432 2314108 Mir193b microRNA 193b gene MP:0010172 abnormal mammary gland epithelium physiology IAGP N RGD:5509061 20160317 MGI PMID:25236432 2314108 Mir193b microRNA 193b gene MP:0012073 premature mammary gland growth during pregnancy IAGP N RGD:5509061 20160317 MGI PMID:25236432 2314274 Cdr1os cerebellar degeneration related antigen 1, opposite strand gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190919 MGI PMID:29887379 2314274 Cdr1os cerebellar degeneration related antigen 1, opposite strand gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20190919 MGI PMID:28798046 2314274 Cdr1os cerebellar degeneration related antigen 1, opposite strand gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20190919 MGI PMID:28798046 2314274 Cdr1os cerebellar degeneration related antigen 1, opposite strand gene MP:0014375 increased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:28798046 2314892 Tctn1 tectonic family member 1 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 2314892 Tctn1 tectonic family member 1 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 2314892 Tctn1 tectonic family member 1 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 2314892 Tctn1 tectonic family member 1 gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:16357211 2314892 Tctn1 tectonic family member 1 gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:16357211 2314892 Tctn1 tectonic family member 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 2314892 Tctn1 tectonic family member 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 2314892 Tctn1 tectonic family member 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:21725307 2314892 Tctn1 tectonic family member 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 2314892 Tctn1 tectonic family member 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20160331 MGI PMID:21725307 2314892 Tctn1 tectonic family member 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 2314892 Tctn1 tectonic family member 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20221215 MGI 2314892 Tctn1 tectonic family member 1 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 2314892 Tctn1 tectonic family member 1 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:21725307 2314892 Tctn1 tectonic family member 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21725307 2314892 Tctn1 tectonic family member 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:16357211 2314892 Tctn1 tectonic family member 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:21725307 2314892 Tctn1 tectonic family member 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:21725307 2314892 Tctn1 tectonic family member 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16357211 2314892 Tctn1 tectonic family member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 2314892 Tctn1 tectonic family member 1 gene MP:0012139 increased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:16357211 2315118 Zbed6 zinc finger, BED type containing 6 gene MP:0001260 increased body weight IAGP N RGD:5509061 20181025 MGI PMID:29440408 2315118 Zbed6 zinc finger, BED type containing 6 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20181025 MGI PMID:29440408 2315118 Zbed6 zinc finger, BED type containing 6 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20181025 MGI PMID:29440408 2315118 Zbed6 zinc finger, BED type containing 6 gene MP:0003398 increased skeletal muscle size IAGP N RGD:5509061 20181025 MGI PMID:29440408 2315118 Zbed6 zinc finger, BED type containing 6 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20181025 MGI PMID:29440408 2315118 Zbed6 zinc finger, BED type containing 6 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20181025 MGI PMID:29440408 2315118 Zbed6 zinc finger, BED type containing 6 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20181025 MGI PMID:29440408 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0010387 abnormal Bergmann glial cell morphology IAGP N RGD:5509061 20200310 MGI PMID:30250269 2315719 Marveld1 MARVEL (membrane-associating) domain containing 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200310 MGI PMID:30250269 30309386 Synb syncytin b gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200625 MGI PMID:22032925 30309386 Synb syncytin b gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20200625 MGI PMID:22032925 30309386 Synb syncytin b gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200625 MGI PMID:22032925 30309386 Synb syncytin b gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20200625 MGI PMID:22032925 30309386 Synb syncytin b gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20200625 MGI PMID:22032925 30309386 Synb syncytin b gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20200625 MGI PMID:22032925 30309386 Synb syncytin b gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200625 MGI PMID:22032925 30309386 Synb syncytin b gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200625 MGI PMID:22032925 30309386 Synb syncytin b gene MP:0011531 abnormal syncytiotrophoblast morphology IAGP N RGD:5509061 20200625 MGI PMID:22032925 30309588 Dido1 death inducer-obliterator 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20200625 MGI PMID:16127461 30309588 Dido1 death inducer-obliterator 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20200625 MGI PMID:16127461 30309588 Dido1 death inducer-obliterator 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20200625 MGI PMID:16127461 30309588 Dido1 death inducer-obliterator 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20221020 MGI PMID:35672775 30309588 Dido1 death inducer-obliterator 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20221020 MGI PMID:35672775 30309588 Dido1 death inducer-obliterator 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20200625 MGI PMID:16127461 30309588 Dido1 death inducer-obliterator 1 gene MP:0001147 small testis IAGP N RGD:5509061 20221020 MGI PMID:35672775 30309588 Dido1 death inducer-obliterator 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20221020 MGI PMID:35672775 30309588 Dido1 death inducer-obliterator 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20221020 MGI PMID:35672775 30309588 Dido1 death inducer-obliterator 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20221020 MGI PMID:35672775 30309588 Dido1 death inducer-obliterator 1 gene MP:0001577 anemia IAGP N RGD:5509061 20200625 MGI PMID:16127461 30309588 Dido1 death inducer-obliterator 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20200625 MGI PMID:21660050 30309588 Dido1 death inducer-obliterator 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20221020 MGI PMID:35672775 30309588 Dido1 death inducer-obliterator 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20200625 MGI PMID:16127461 30309588 Dido1 death inducer-obliterator 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200625 MGI PMID:16127461 30309588 Dido1 death inducer-obliterator 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20221020 MGI PMID:35672775 30309588 Dido1 death inducer-obliterator 1 gene MP:0002064 seizures IAGP N RGD:5509061 20221020 MGI PMID:35672775 30309588 Dido1 death inducer-obliterator 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20200625 MGI PMID:16127461 30309588 Dido1 death inducer-obliterator 1 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20200625 MGI PMID:16127461 30309588 Dido1 death inducer-obliterator 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20221020 MGI PMID:35672775 30309588 Dido1 death inducer-obliterator 1 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20200625 MGI PMID:16127461 30309588 Dido1 death inducer-obliterator 1 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20200625 MGI PMID:21660050 30309588 Dido1 death inducer-obliterator 1 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20200625 MGI PMID:21660050 30309588 Dido1 death inducer-obliterator 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20200625 MGI PMID:21660050 30309588 Dido1 death inducer-obliterator 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20200625 MGI PMID:21660050 30309588 Dido1 death inducer-obliterator 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20221020 MGI PMID:35672775 30309588 Dido1 death inducer-obliterator 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20200625 MGI PMID:16127461 30309588 Dido1 death inducer-obliterator 1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20200625 MGI PMID:21660050 30309588 Dido1 death inducer-obliterator 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20221020 MGI PMID:35672775 30309588 Dido1 death inducer-obliterator 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20221020 MGI PMID:35672775 30309588 Dido1 death inducer-obliterator 1 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20200625 MGI PMID:16127461 30309588 Dido1 death inducer-obliterator 1 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20200625 MGI PMID:16127461 30309588 Dido1 death inducer-obliterator 1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20200625 MGI PMID:16127461 30309588 Dido1 death inducer-obliterator 1 gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20200625 MGI PMID:21660050 30309588 Dido1 death inducer-obliterator 1 gene MP:0009332 abnormal splenocyte morphology IAGP N RGD:5509061 20200625 MGI PMID:16127461 30309588 Dido1 death inducer-obliterator 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20200625 MGI PMID:21660050 30309588 Dido1 death inducer-obliterator 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200625 MGI PMID:21660050 30309588 Dido1 death inducer-obliterator 1 gene MP:0011191 increased embryonic epiblast cell apoptosis IAGP N RGD:5509061 20200625 MGI PMID:21660050 30309588 Dido1 death inducer-obliterator 1 gene MP:0011192 decreased embryonic epiblast cell proliferation IAGP N RGD:5509061 20200625 MGI PMID:21660050 30309588 Dido1 death inducer-obliterator 1 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20221020 MGI PMID:35672775 30309588 Dido1 death inducer-obliterator 1 gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20221020 MGI PMID:35672775 30309588 Dido1 death inducer-obliterator 1 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20200625 MGI PMID:21660050 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0000189 hypoglycemia IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0000479 abnormal enterocyte morphology IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0000745 tremors IAGP N RGD:5509061 20200625 MGI PMID:1634998 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0000920 abnormal myelination IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0000921 demyelination IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20200625 MGI PMID:1634998 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200625 MGI PMID:1382814 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200625 MGI PMID:1634998 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20200625 MGI PMID:24413176 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20200625 MGI PMID:24413176 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001393 ataxia IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20200625 MGI PMID:1634998 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20200625 MGI PMID:1634998 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20200625 MGI PMID:24413176 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20200625 MGI PMID:1634998 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20200625 MGI PMID:1634998 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200625 MGI PMID:1634998 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20200625 MGI PMID:24413176 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001524 impaired limb coordination IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001732 postnatal growth retardation IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0001961 abnormal reflex IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0002082 postnatal lethality IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200625 MGI PMID:1634998 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20200625 MGI PMID:24413176 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20200625 MGI PMID:24413176 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0002883 chromatolysis IAGP N RGD:5509061 20200625 MGI PMID:1634998 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20200625 MGI PMID:1634998 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20200625 MGI PMID:24413176 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200625 MGI PMID:24413176 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200625 MGI PMID:24413176 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20200625 MGI PMID:1634998 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20200625 MGI PMID:24413176 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20200625 MGI PMID:4388883 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20200625 MGI PMID:4388883 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20221215 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20200625 MGI PMID:1382814 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0008025 brain vacuoles IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0008027 abnormal spinal cord white matter morphology IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200625 MGI PMID:24413176 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200625 MGI PMID:24413176 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20200625 MGI PMID:24413176 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200625 MGI PMID:24413176 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200625 MGI PMID:28839191 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0009148 pancreas necrosis IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0011083 lethality at weaning, complete penetrance IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0011084 lethality at weaning, incomplete penetrance IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0011085 postnatal lethality, complete penetrance IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200625 MGI 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200625 MGI PMID:24413176 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0013722 abnormal circulating tyrosine level IAGP N RGD:5509061 20240801 MGI PMID:4388883 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0014333 short retina cone cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:28839191 30309656 Atp8a2 ATPase, aminophospholipid transporter-like, class I, type 8A, member 2 gene MP:0030670 increased circulating phenylalanine level IAGP N RGD:5509061 20240801 MGI PMID:4388883 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0000445 short snout IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20220519 MGI 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200625 MGI 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0000914 exencephaly IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0001147 small testis IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0001293 anophthalmia IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20200625 MGI PMID:18163532 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200625 MGI 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0002581 abnormal ileum morphology IEA N RGD:5509061 20220519 MGI 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0003078 aphakia IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200625 MGI PMID:18163532 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20200625 MGI PMID:18163532 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0004266 pale placenta IAGP N RGD:5509061 20200625 MGI PMID:18163532 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0004380 short frontal bone IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0004471 short nasal bone IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20200625 MGI PMID:18163532 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200625 MGI PMID:22965116 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0008524 increased plasmacytoid dendritic cell number IEA N RGD:5509061 20230601 MGI 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0008957 abnormal placenta junctional zone morphology IAGP N RGD:5509061 20200625 MGI PMID:18163532 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20200625 MGI PMID:18163532 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0010769 abnormal survival IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20200625 MGI PMID:18163532 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0012101 acoria IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0012109 decreased trophoblast glycogen cell number IAGP N RGD:5509061 20200625 MGI PMID:18163532 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0013678 decreased Ly6C-positive NK T cell number IEA N RGD:5509061 20240523 MGI 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0030189 broad snout IAGP N RGD:5509061 20200625 MGI PMID:21072209 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20200625 MGI PMID:18163532 30309698 Alkbh1 alkB homolog 1, histone H2A dioxygenase gene MP:0031428 lens dislocation IAGP N RGD:5509061 20220714 MGI PMID:21072209 32722601 Ece2 endothelin converting enzyme 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20200702 MGI PMID:10811845 32722601 Ece2 endothelin converting enzyme 2 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20200702 MGI PMID:10811845 32722601 Ece2 endothelin converting enzyme 2 gene MP:0000299 failure of atrioventricular cushion closure IAGP N RGD:5509061 20200702 MGI PMID:10811845 32722601 Ece2 endothelin converting enzyme 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20200702 MGI PMID:10811845 32722601 Ece2 endothelin converting enzyme 2 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20200702 MGI PMID:10811845 32722601 Ece2 endothelin converting enzyme 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200702 MGI PMID:10811845 32722601 Ece2 endothelin converting enzyme 2 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20200702 MGI PMID:10811845 32722601 Ece2 endothelin converting enzyme 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20200702 MGI PMID:10811845 32722601 Ece2 endothelin converting enzyme 2 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20200702 MGI PMID:10811845 32722601 Ece2 endothelin converting enzyme 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20200702 MGI PMID:10811845 32722601 Ece2 endothelin converting enzyme 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20200702 MGI PMID:10811845 32722601 Ece2 endothelin converting enzyme 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200702 MGI PMID:10811845 32722601 Ece2 endothelin converting enzyme 2 gene MP:0031550 abnormal atrioventricular valve development IAGP N RGD:5509061 20240104 MGI PMID:10811845 32722963 Atrip ATR interacting protein gene MP:0000433 microcephaly IAGP N RGD:5509061 20210204 MGI PMID:33110058 32722963 Atrip ATR interacting protein gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20210204 MGI PMID:33110058 32722963 Atrip ATR interacting protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210204 MGI PMID:33110058 32722963 Atrip ATR interacting protein gene MP:0001297 microphthalmia IAGP N RGD:5509061 20210204 MGI PMID:33110058 32722963 Atrip ATR interacting protein gene MP:0001297 microphthalmia IAGP N RGD:5509061 20210218 MGI PMID:32994318 32722963 Atrip ATR interacting protein gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20210218 MGI PMID:32994318 32722963 Atrip ATR interacting protein gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20210204 MGI PMID:33110058 32722963 Atrip ATR interacting protein gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 32722963 Atrip ATR interacting protein gene MP:0003078 aphakia IAGP N RGD:5509061 20210204 MGI PMID:33110058 32722963 Atrip ATR interacting protein gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20210204 MGI PMID:33110058 32722963 Atrip ATR interacting protein gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20210218 MGI PMID:32994318 32722963 Atrip ATR interacting protein gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20210204 MGI PMID:33110058 32722963 Atrip ATR interacting protein gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20210218 MGI PMID:32994318 32722963 Atrip ATR interacting protein gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20210204 MGI PMID:33110058 32722963 Atrip ATR interacting protein gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 32722963 Atrip ATR interacting protein gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20210218 MGI PMID:32994318 32722963 Atrip ATR interacting protein gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20210218 MGI PMID:32994318 32722963 Atrip ATR interacting protein gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20210218 MGI PMID:32994318 32722963 Atrip ATR interacting protein gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20210218 MGI PMID:32994318 32722963 Atrip ATR interacting protein gene MP:0008794 increased lens epithelium apoptosis IAGP N RGD:5509061 20210204 MGI PMID:33110058 32722963 Atrip ATR interacting protein gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20210204 MGI PMID:33110058 32722963 Atrip ATR interacting protein gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20210204 MGI PMID:33110058 32722963 Atrip ATR interacting protein gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20200702 MGI 32722963 Atrip ATR interacting protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 32722963 Atrip ATR interacting protein gene MP:0020596 decreased cerebral cortex total cell area IAGP N RGD:5509061 20210204 MGI PMID:33110058 32722963 Atrip ATR interacting protein gene MP:0020621 decreased dorsal striatum total cell area IAGP N RGD:5509061 20210204 MGI PMID:33110058 32722963 Atrip ATR interacting protein gene MP:0030004 hippocampus hypoplasia IAGP N RGD:5509061 20210204 MGI PMID:33110058 32722963 Atrip ATR interacting protein gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20210218 MGI PMID:32994318 3587874 Btbd18 BTB domain containing 18 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 3587874 Btbd18 BTB domain containing 18 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 3587874 Btbd18 BTB domain containing 18 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 3587874 Btbd18 BTB domain containing 18 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 3587874 Btbd18 BTB domain containing 18 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 3587874 Btbd18 BTB domain containing 18 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 3587874 Btbd18 BTB domain containing 18 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 3587874 Btbd18 BTB domain containing 18 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 3587874 Btbd18 BTB domain containing 18 gene MP:0001147 small testis IAGP N RGD:5509061 20170601 MGI PMID:28292424 3587874 Btbd18 BTB domain containing 18 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20170601 MGI PMID:28292424 3587874 Btbd18 BTB domain containing 18 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20230119 MGI 3587874 Btbd18 BTB domain containing 18 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20230119 MGI 3587874 Btbd18 BTB domain containing 18 gene MP:0001925 male infertility IAGP N RGD:5509061 20170601 MGI PMID:28292424 3587874 Btbd18 BTB domain containing 18 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20170601 MGI PMID:28292424 3587874 Btbd18 BTB domain containing 18 gene MP:0003641 small lung IEA N RGD:5509061 20230119 MGI 3587874 Btbd18 BTB domain containing 18 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20170601 MGI PMID:28292424 3587874 Btbd18 BTB domain containing 18 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20170601 MGI PMID:28292424 3587874 Btbd18 BTB domain containing 18 gene MP:0005159 azoospermia IAGP N RGD:5509061 20170601 MGI PMID:28292424 3587874 Btbd18 BTB domain containing 18 gene MP:0005380 embryo phenotype IAGP N RGD:5509061 20240111 MGI PMID:28292424 3587874 Btbd18 BTB domain containing 18 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20170601 MGI PMID:28292424 3587874 Btbd18 BTB domain containing 18 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20170601 MGI PMID:28292424 3587874 Btbd18 BTB domain containing 18 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20170601 MGI PMID:28292424 3587874 Btbd18 BTB domain containing 18 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20170601 MGI PMID:28292424 3731974 Asmt acetylserotonin O-methyltransferase gene MP:0004851 increased testis weight IAGP N RGD:5509061 20180705 MGI PMID:20308563 3731974 Asmt acetylserotonin O-methyltransferase gene MP:0011729 abnormal pineal gland melatonin secretion IAGP N RGD:5509061 20180705 MGI PMID:20308563 3799608 Hoxb3os homeobox B3 and homeobox B2, opposite strand gene MP:0003675 kidney cyst IAGP N RGD:5509061 20240328 MGI PMID:37953472 3799608 Hoxb3os homeobox B3 and homeobox B2, opposite strand gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20240328 MGI PMID:37953472 39128206 Lwq18_m liver weight QTL 18 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20200925 MGI Created by mouse qtl pipeline PMID:15058381 39128207 Lwq16_m liver weight QTL 16 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20200925 MGI Created by mouse qtl pipeline PMID:15058381 39128208 Lwq15_m liver weight QTL 15 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20200925 MGI Created by mouse qtl pipeline PMID:15058381 39128209 Lwq14_m liver weight QTL 14 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20200925 MGI Created by mouse qtl pipeline PMID:15058381 39128210 Lwq19_m liver weight QTL 19 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20200925 MGI Created by mouse qtl pipeline PMID:15058381 39128211 Lwq22_m liver weight QTL 22 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20200925 MGI Created by mouse qtl pipeline PMID:15058381 39128212 Lwq21_m liver weight QTL 21 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20200925 MGI Created by mouse qtl pipeline PMID:15058381 39128213 Lwq23_m liver weight QTL 10 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20200925 MGI Created by mouse qtl pipeline PMID:15058381 39128214 Lwq20_m liver weight QTL 20 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20200925 MGI Created by mouse qtl pipeline PMID:15058381 39128215 Lwq17_m liver weight QTL 17 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20200925 MGI Created by mouse qtl pipeline PMID:15058381 39128216 Lwq24_m liver weight QTL 24 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20200925 MGI Created by mouse qtl pipeline PMID:17517159 39128216 Lwq24_m liver weight QTL 24 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17517159 39129335 Gm41261 predicted gene, 41261 gene MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20240523 MGI PMID:38373108 39129335 Gm41261 predicted gene, 41261 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20240523 MGI PMID:38373108 39129335 Gm41261 predicted gene, 41261 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20240523 MGI PMID:38373108 39129335 Gm41261 predicted gene, 41261 gene MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20240523 MGI PMID:38373108 39129335 Gm41261 predicted gene, 41261 gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240523 MGI PMID:38373108 39129335 Gm41261 predicted gene, 41261 gene MP:0020157 abnormal behavioral response to alcohol IAGP N RGD:5509061 20240523 MGI PMID:38373108 39130311 Rdur RIG-I dependent antiviral response regulator RNA gene MP:0002418 increased susceptibility to viral infection IAGP N RGD:5509061 20231102 MGI PMID:34054851 39130311 Rdur RIG-I dependent antiviral response regulator RNA gene MP:0008591 increased circulating interleukin-1 level IAGP N RGD:5509061 20231102 MGI PMID:34054851 39130311 Rdur RIG-I dependent antiviral response regulator RNA gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20231102 MGI PMID:34054851 39130311 Rdur RIG-I dependent antiviral response regulator RNA gene MP:0009791 increased susceptibility to viral infection induced morbidity/mortality IAGP N RGD:5509061 20231102 MGI PMID:34054851 39130311 Rdur RIG-I dependent antiviral response regulator RNA gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20231102 MGI PMID:34054851 405649854 Chapir cardiac-hypertrophy-associated piRNA gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20240516 MGI PMID:33020597 407444535 Mir503hg Mir503, Mir351, and Mir322 host gene gene MP:0000231 hypertension IAGP N RGD:5509061 20240822 MGI PMID:36929003 407444535 Mir503hg Mir503, Mir351, and Mir322 host gene gene MP:0000274 enlarged heart IAGP N RGD:5509061 20240822 MGI PMID:36929003 407444535 Mir503hg Mir503, Mir351, and Mir322 host gene gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20240822 MGI PMID:36929003 407444535 Mir503hg Mir503, Mir351, and Mir322 host gene gene MP:0002833 increased heart weight IAGP N RGD:5509061 20240822 MGI PMID:36929003 407444535 Mir503hg Mir503, Mir351, and Mir322 host gene gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20240822 MGI PMID:36929003 407444535 Mir503hg Mir503, Mir351, and Mir322 host gene gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20240822 MGI PMID:36929003 407444535 Mir503hg Mir503, Mir351, and Mir322 host gene gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20240822 MGI PMID:36929003 407444535 Mir503hg Mir503, Mir351, and Mir322 host gene gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20240822 MGI PMID:36929003 407444535 Mir503hg Mir503, Mir351, and Mir322 host gene gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20240822 MGI PMID:36929003 407570911 Aldh3b2 aldehyde dehydrogenase 3 family, member B2 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20240926 MGI PMID:34370553 407570911 Aldh3b2 aldehyde dehydrogenase 3 family, member B2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20240926 MGI PMID:34370553 407570911 Aldh3b2 aldehyde dehydrogenase 3 family, member B2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240926 MGI PMID:34370553 407570911 Aldh3b2 aldehyde dehydrogenase 3 family, member B2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240926 MGI PMID:34370553 407570911 Aldh3b2 aldehyde dehydrogenase 3 family, member B2 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20240926 MGI PMID:34370553 407570911 Aldh3b2 aldehyde dehydrogenase 3 family, member B2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20240926 MGI PMID:34370553 407570911 Aldh3b2 aldehyde dehydrogenase 3 family, member B2 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20240926 MGI PMID:34370553 407570911 Aldh3b2 aldehyde dehydrogenase 3 family, member B2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20240926 MGI PMID:34370553 407570911 Aldh3b2 aldehyde dehydrogenase 3 family, member B2 gene MP:0020583 decreased ceramide level IAGP N RGD:5509061 20240926 MGI PMID:34370553 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20240926 MGI PMID:16740480 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20240926 MGI PMID:16740480 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240926 MGI PMID:16740480 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20240926 MGI PMID:16740480 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20240926 MGI PMID:16740480 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20240926 MGI PMID:16740480 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20240926 MGI PMID:23897694 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20240926 MGI PMID:16740480 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20240926 MGI PMID:16819522 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20240926 MGI PMID:16908842 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20240926 MGI PMID:16740480 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20240926 MGI PMID:16740480 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20240926 MGI PMID:16740480 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0010477 coronary artery aneurysm IAGP N RGD:5509061 20240926 MGI PMID:23897694 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0011655 abnormal systemic artery morphology IAGP N RGD:5509061 20240926 MGI PMID:23897694 407571016 Gipc1 GIPC PDZ domain containing family, member 1 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20240926 MGI PMID:16740480 4080496 Npcd neuronal pentraxin chromo domain gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 4080496 Npcd neuronal pentraxin chromo domain gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210826 MGI 4080496 Npcd neuronal pentraxin chromo domain gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20230601 MGI 4080496 Npcd neuronal pentraxin chromo domain gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20220811 MGI 408345569 Plekhh1 pleckstrin homology domain containing, family H (with MyTH4 domain) member 1 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20241031 MGI 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20241031 MGI PMID:17143286 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0000091 short premaxilla IAGP N RGD:5509061 20241031 MGI PMID:17143286 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0000097 short maxilla IAGP N RGD:5509061 20241031 MGI PMID:17143286 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20241031 MGI PMID:17143286 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20241031 MGI PMID:17143286 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0000445 short snout IAGP N RGD:5509061 20241031 MGI PMID:17143286 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20241031 MGI PMID:19056881 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20241031 MGI PMID:19056881 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0001127 small ovary IAGP N RGD:5509061 20241031 MGI PMID:19056881 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0001926 female infertility IAGP N RGD:5509061 20241031 MGI PMID:19056881 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20241031 MGI PMID:19056881 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0004471 short nasal bone IAGP N RGD:5509061 20241031 MGI PMID:17143286 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20241031 MGI PMID:19056881 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20241031 MGI PMID:17143286 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20241031 MGI PMID:19056881 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20241031 MGI PMID:17143286 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0008869 anovulation IAGP N RGD:5509061 20241031 MGI PMID:19056881 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0009370 decreased theca cell number IAGP N RGD:5509061 20241031 MGI PMID:19056881 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20241031 MGI PMID:17143286 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20241031 MGI PMID:19056881 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0011709 increased fibroblast cell migration IAGP N RGD:5509061 20241031 MGI PMID:17143286 408345745 2610005L07Rik RIKEN cDNA 2610005L07 gene gene MP:0030189 broad snout IAGP N RGD:5509061 20241031 MGI PMID:17143286 408346031 Norad non-coding RNA activated by DNA damage gene MP:0000160 kyphosis IAGP N RGD:5509061 20241031 MGI PMID:35304463 408346031 Norad non-coding RNA activated by DNA damage gene MP:0003786 premature aging IAGP N RGD:5509061 20241031 MGI PMID:35304463 408346031 Norad non-coding RNA activated by DNA damage gene MP:0004684 intervertebral disk degeneration IAGP N RGD:5509061 20241031 MGI PMID:35304463 408346031 Norad non-coding RNA activated by DNA damage gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20241031 MGI PMID:35304463 408346031 Norad non-coding RNA activated by DNA damage gene MP:0006392 abnormal nucleus pulposus morphology IAGP N RGD:5509061 20241031 MGI PMID:35304463 408346718 Zscan12 zinc finger and SCAN domain containing 12 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20241031 MGI 4085978 BY367451 cDNA sequence, BY367451 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:17005861 4085978 BY367451 cDNA sequence, BY367451 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17005861 4085978 BY367451 cDNA sequence, BY367451 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17005861 4109631 Tsga8 testis specific gene A8 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20210812 MGI PMID:33766931 4109631 Tsga8 testis specific gene A8 gene MP:0001925 male infertility IAGP N RGD:5509061 20210812 MGI PMID:33766931 4109631 Tsga8 testis specific gene A8 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20210812 MGI PMID:33766931 4109631 Tsga8 testis specific gene A8 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210812 MGI PMID:33766931 4109631 Tsga8 testis specific gene A8 gene MP:0005159 azoospermia IAGP N RGD:5509061 20210812 MGI PMID:33766931 4109631 Tsga8 testis specific gene A8 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20210812 MGI PMID:33766931 4109631 Tsga8 testis specific gene A8 gene MP:0009852 increased Sertoli cell phagocytosis IAGP N RGD:5509061 20210812 MGI PMID:33766931 4109631 Tsga8 testis specific gene A8 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20210812 MGI PMID:33766931 4140952 Kcal3_m kilocalorie 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12388789 4140952 Kcal3_m kilocalorie 3 (mouse) qtl MP:0011939 increased food intake IAGP N RGD:5509061 20130328 MGI PMID:12388789 4140953 Cq6_m cholesterol QTL 6 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:15524312 4140953 Cq6_m cholesterol QTL 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15524312 4140955 Plgr1_m plague resistance locus 1 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:18573896 4140955 Plgr1_m plague resistance locus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18573896 4140956 Ath26_m atherosclerosis 26 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16373612 4140956 Ath26_m atherosclerosis 26 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16373612|PMID:17641228 4140956 Ath26_m atherosclerosis 26 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20151218 MGI Created by mouse qtl pipeline PMID:16373612 4140958 Hemq1_m hematocrit QTL 1 (mouse) qtl MP:0002608 increased hematocrit IAGP N RGD:5509061 20111116 MGI PMID:16783647 4140958 Hemq1_m hematocrit QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783647 4140959 W10q17_m weight 10 weeks QTL 17 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4140959 W10q17_m weight 10 weeks QTL 17 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4140960 Bmrbc2_m bone marrow RBC 2 (mouse) qtl MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:17185011 4140960 Bmrbc2_m bone marrow RBC 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17185011 4140961 Brabq1_m brain amyloid beta QTL 1 (mouse) qtl MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20111116 MGI PMID:17400334 4140961 Brabq1_m brain amyloid beta QTL 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17400334 4140961 Brabq1_m brain amyloid beta QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20140718 MGI Created by mouse qtl pipeline PMID:17400334 4140961 Brabq1_m brain amyloid beta QTL 1 (mouse) qtl MP:0005395 obsolete other phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17400334 4140962 Mleu2_m myeloid leukemia survival 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4140962 Mleu2_m myeloid leukemia survival 2 (mouse) qtl MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20111116 MGI PMID:18552208 4140963 Rmp2_m resistance to mousepox 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:2002550|PMID:1433507 4140963 Rmp2_m resistance to mousepox 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20151023 MGI Created by mouse qtl pipeline PMID:2002550 4140963 Rmp2_m resistance to mousepox 2 (mouse) qtl MP:0020928 increased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:2002550 4140965 Exz1_m adrenal X zone degeneration 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:3582592 4140965 Exz1_m adrenal X zone degeneration 1 (mouse) qtl MP:0008303 early degeneration of the adrenal gland x-zone IAGP N RGD:5509061 20111116 MGI PMID:3582592 4140966 Egq12_m early growth QTL 12 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4140966 Egq12_m early growth QTL 12 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4140967 Bmd39_m bone mineral density 39 (mouse) qtl MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20111116 MGI PMID:17371164 4140967 Bmd39_m bone mineral density 39 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17371164 4140968 Mpdk6_m modifier of polycystic kidney disease 6 (mouse) qtl MP:0003253 dilated bile duct IAGP N RGD:5509061 20111116 MGI PMID:15728779 4140968 Mpdk6_m modifier of polycystic kidney disease 6 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15728779 4140968 Mpdk6_m modifier of polycystic kidney disease 6 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15728779 4140969 Chcmq2_m mean cell hemoglobin concentration QTL 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16596451 4140969 Chcmq2_m mean cell hemoglobin concentration QTL 2 (mouse) qtl MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20111116 MGI PMID:16596451 4140975 Psrs3_m psoriasis susceptibility 3 (mouse) qtl MP:0001193 psoriasis IAGP N RGD:5509061 20111116 MGI PMID:16982899 4140975 Psrs3_m psoriasis susceptibility 3 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16982899 4140978 Nilac5_m nicotine induced locomotor activity 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16176386 4140978 Nilac5_m nicotine induced locomotor activity 5 (mouse) qtl MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:16176386 4140979 Vmmt11_m vertebral morphology and mechanical traits 11 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4140979 Vmmt11_m vertebral morphology and mechanical traits 11 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4140980 Mvwf2_m modifier of von Willebrand factor 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17155961 4140980 Mvwf2_m modifier of von Willebrand factor 2 (mouse) qtl MP:0031165 increased circulating von Willebrand factor level IAGP N RGD:5509061 20201015 MGI PMID:17155961 4140981 Mpvq1_m mean platelet volume locus 1 (mouse) qtl MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20111116 MGI PMID:16261417 4140981 Mpvq1_m mean platelet volume locus 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4140984 Bglu11_m blood glucose level 11 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4140984 Bglu11_m blood glucose level 11 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4140985 Bwt1_m body weight 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15870393 4140985 Bwt1_m body weight 1 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:15870393 4140987 Chlq6_m circulating hormone level QTL 6 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:12865502 4140987 Chlq6_m circulating hormone level QTL 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12865502 4140988 Abshq5_m abnormal sperm head QTL 5 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18689897 4140988 Abshq5_m abnormal sperm head QTL 5 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18689897 4140988 Abshq5_m abnormal sperm head QTL 5 (mouse) qtl MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20111116 MGI PMID:18689897 4140990 Lgq6_m late growth QTL 6 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4140990 Lgq6_m late growth QTL 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4140991 Bglu5_m blood glucose level 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4140991 Bglu5_m blood glucose level 5 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4140992 Actre5_m activity response to ethanol 5 (mouse) qtl MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20111116 MGI PMID:17143586 4140992 Actre5_m activity response to ethanol 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17143586 4140993 Tglq2b_m triglyceride QTL 2b (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17496333 4140995 Fbtq6_m femoral bone trait QTL 6 (mouse) qtl MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20111116 MGI PMID:14584885 4140995 Fbtq6_m femoral bone trait QTL 6 (mouse) qtl MP:0003795 abnormal bone structure IAGP N RGD:5509061 20111116 MGI PMID:14584885 4140995 Fbtq6_m femoral bone trait QTL 6 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:14584885 4140995 Fbtq6_m femoral bone trait QTL 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14584885 4140996 Bwtq8_m body weight QTL 8 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4140996 Bwtq8_m body weight QTL 8 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141000 Nidd3_m non-insulin-dependent diabetes mellitus 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:9703330 4141000 Nidd3_m non-insulin-dependent diabetes mellitus 3 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:9703330 4141000 Nidd3_m non-insulin-dependent diabetes mellitus 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9703330 4141000 Nidd3_m non-insulin-dependent diabetes mellitus 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9703330 4141001 Tgq17_m triglyceride QTL 17 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4141001 Tgq17_m triglyceride QTL 17 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4141002 Nhil4_m non-heme iron levels 4 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16799992 4141002 Nhil4_m non-heme iron levels 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16799992 4141002 Nhil4_m non-heme iron levels 4 (mouse) qtl MP:0008807 increased liver iron level IAGP N RGD:5509061 20111116 MGI PMID:16799992 4141003 Ramls1_m radiation-induced acute myeloid leukemia sensitivity 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12411293 4141003 Ramls1_m radiation-induced acute myeloid leukemia sensitivity 1 (mouse) qtl MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20111116 MGI PMID:12411293 4141004 Scl2_m susceptibility to cutaneous leishmaniasis 2 (mouse) qtl MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:2212703 4141004 Scl2_m susceptibility to cutaneous leishmaniasis 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:2212703 4141009 Dbsq3_m diabetes susceptibility QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16919419 4141009 Dbsq3_m diabetes susceptibility QTL 3 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:16919419 4141015 Dmq4_m diet and mammary tumor QTL 4 (mouse) qtl MP:0001272 increased metastatic potential IAGP N RGD:5509061 20111116 MGI PMID:18288525 4141015 Dmq4_m diet and mammary tumor QTL 4 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18288525 4141016 Chldq3_m cholesterol and HDL QTL 3 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16254318 4141016 Chldq3_m cholesterol and HDL QTL 3 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:17496333 4141016 Chldq3_m cholesterol and HDL QTL 3 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16254318 4141016 Chldq3_m cholesterol and HDL QTL 3 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:17496333 4141016 Chldq3_m cholesterol and HDL QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16254318|PMID:17496333 4141016 Chldq3_m cholesterol and HDL QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:16254318 4141019 Tgq29_m triglyceride QTL 29 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4141019 Tgq29_m triglyceride QTL 29 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4141020 Ascla1_m atherosclerotic lesion area 1 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16380418 4141020 Ascla1_m atherosclerotic lesion area 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16380418 4141024 Bglu10_m blood glucose level 10 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4141024 Bglu10_m blood glucose level 10 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4141025 Mtbcq4_m multiple trait body composition QTL 4 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141025 Mtbcq4_m multiple trait body composition QTL 4 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141025 Mtbcq4_m multiple trait body composition QTL 4 (mouse) qtl MP:0003397 increased muscle weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141025 Mtbcq4_m multiple trait body composition QTL 4 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4141025 Mtbcq4_m multiple trait body composition QTL 4 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4141025 Mtbcq4_m multiple trait body composition QTL 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4141025 Mtbcq4_m multiple trait body composition QTL 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4141025 Mtbcq4_m multiple trait body composition QTL 4 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141025 Mtbcq4_m multiple trait body composition QTL 4 (mouse) qtl MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141027 Litsq_m litter size QTL (mouse) qtl MP:0001934 increased litter size IAGP N RGD:5509061 20111116 MGI PMID:18239664 4141027 Litsq_m litter size QTL (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18239664 4141028 Mclr_m methylcholanthrene lymphoma resistance (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:2783886 4141028 Mclr_m methylcholanthrene lymphoma resistance (mouse) qtl MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20111116 MGI PMID:2783886 4141028 Mclr_m methylcholanthrene lymphoma resistance (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:2783886 4141028 Mclr_m methylcholanthrene lymphoma resistance (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20241101 MGI Created by mouse qtl pipeline PMID:2783886 4141028 Mclr_m methylcholanthrene lymphoma resistance (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20241101 MGI Created by mouse qtl pipeline PMID:2783886 4141030 Nilac6_m nicotine induced locomotor activity 6 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16176386 4141030 Nilac6_m nicotine induced locomotor activity 6 (mouse) qtl MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:16176386 4141031 Pltq1_m platelet quantitative locus 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4141031 Pltq1_m platelet quantitative locus 1 (mouse) qtl MP:0005505 thrombocytosis IAGP N RGD:5509061 20111116 MGI PMID:16261417 4141032 Wbcc1_m white blood cell count 1 (mouse) qtl MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:18552208 4141032 Wbcc1_m white blood cell count 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141032 Wbcc1_m white blood cell count 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141033 Wg2d_m weight gain in high growth mice 2d (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17694346 4141033 Wg2d_m weight gain in high growth mice 2d (mouse) qtl MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:17694346 4141034 Bmd1c_m bone mineral density 1c (mouse) qtl MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:16355278 4141034 Bmd1c_m bone mineral density 1c (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16355278 4141034 Bmd1c_m bone mineral density 1c (mouse) qtl MP:0003795 abnormal bone structure IAGP N RGD:5509061 20111116 MGI PMID:16355278 4141034 Bmd1c_m bone mineral density 1c (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16355278 4141034 Bmd1c_m bone mineral density 1c (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16355278 4141035 Asdq7_m atrial septal defect QTL 7 (mouse) qtl MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20111116 MGI PMID:16484617 4141035 Asdq7_m atrial septal defect QTL 7 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16484617 4141038 Acla1_m anticardiolipin antibody 1 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:9754557 4141038 Acla1_m anticardiolipin antibody 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9754557 4141039 Hom1_m hormone metabolism 1 (mouse) qtl MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20111116 MGI PMID:4507168 4141039 Hom1_m hormone metabolism 1 (mouse) qtl MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20111116 MGI PMID:4695943 4141039 Hom1_m hormone metabolism 1 (mouse) qtl MP:0004851 increased testis weight IAGP N RGD:5509061 20111116 MGI PMID:4695943 4141039 Hom1_m hormone metabolism 1 (mouse) qtl MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20111116 MGI PMID:4695943 4141039 Hom1_m hormone metabolism 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:4507168|PMID:4695943 4141039 Hom1_m hormone metabolism 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20131011 MGI Created by mouse qtl pipeline PMID:4695943|PMID:4507168 4141039 Hom1_m hormone metabolism 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:4507168|PMID:4695943 4141039 Hom1_m hormone metabolism 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20131011 MGI Created by mouse qtl pipeline PMID:4695943|PMID:4507168 4141039 Hom1_m hormone metabolism 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:4507168|PMID:4695943 4141039 Hom1_m hormone metabolism 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20131011 MGI Created by mouse qtl pipeline PMID:4695943|PMID:4507168 4141040 Hmtb9_m hemostasis and thrombosis rebleeding time 9 (mouse) qtl MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20111116 MGI PMID:18787898 4141040 Hmtb9_m hemostasis and thrombosis rebleeding time 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18787898 4141042 Ril2_m radiation-induced leukemia sensitivity 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6270228 4141042 Ril2_m radiation-induced leukemia sensitivity 2 (mouse) qtl MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20111116 MGI PMID:6270228 4141042 Ril2_m radiation-induced leukemia sensitivity 2 (mouse) qtl MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20111116 MGI PMID:6270228 4141042 Ril2_m radiation-induced leukemia sensitivity 2 (mouse) qtl MP:0004503 decreased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20111116 MGI PMID:6270228 4141043 Fatmq2_m total fat pad mass QTL 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4141043 Fatmq2_m total fat pad mass QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:17110492 4141043 Fatmq2_m total fat pad mass QTL 2 (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:17110492 4141047 Nilac1_m nicotine induced locomotor activity 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16176386 4141047 Nilac1_m nicotine induced locomotor activity 1 (mouse) qtl MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:16176386 4141047 Nilac1_m nicotine induced locomotor activity 1 (mouse) qtl MP:0009756 impaired behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:19083055 4141048 Mpdk7_m modifier of polycystic kidney disease 7 (mouse) qtl MP:0003254 bile duct inflammation IAGP N RGD:5509061 20111116 MGI PMID:15728779 4141048 Mpdk7_m modifier of polycystic kidney disease 7 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15728779 4141048 Mpdk7_m modifier of polycystic kidney disease 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15728779 4141049 Ltsw2_m low testis weight 2 (mouse) qtl MP:0004852 decreased testis weight IAGP N RGD:5509061 20111116 MGI PMID:17483418 4141049 Ltsw2_m low testis weight 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17483418 4141049 Ltsw2_m low testis weight 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17483418 4141050 Mssq20_m mandible size and shape QTL 20 (mouse) qtl MP:0004592 small mandible IAGP N RGD:5509061 20111116 MGI PMID:19067046 4141050 Mssq20_m mandible size and shape QTL 20 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141050 Mssq20_m mandible size and shape QTL 20 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141054 mwfh_m modifier of white forlock hypopigmentation (mouse) qtl MP:0001186 pigmentation phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10077527 4141054 mwfh_m modifier of white forlock hypopigmentation (mouse) qtl MP:0005408 hypopigmentation IAGP N RGD:5509061 20111116 MGI PMID:10077527 4141056 Lskcn2_m LSK cell number 2 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:14988159 4141056 Lskcn2_m LSK cell number 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14988159 4141057 Brwt1_m brain weight 1 (mouse) qtl MP:0002176 increased brain weight IAGP N RGD:5509061 20111116 MGI PMID:1393606 4141057 Brwt1_m brain weight 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1393606 4141058 Blmpf3_m bleomycin-induced pulmonary fibrosis 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:16179420 4141058 Blmpf3_m bleomycin-induced pulmonary fibrosis 3 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16179420 4141058 Blmpf3_m bleomycin-induced pulmonary fibrosis 3 (mouse) qtl MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20111116 MGI PMID:16179420 4141059 Ciaaq1_m collagen induced arthritis autoantibody QTL 1 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:17361202 4141059 Ciaaq1_m collagen induced arthritis autoantibody QTL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17361202 4141060 Pbwg19_m postnatal body weight growth 19 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 4141060 Pbwg19_m postnatal body weight growth 19 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16174331 4141062 Obwq5_m obesity and body weight QTL 5 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141062 Obwq5_m obesity and body weight QTL 5 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141062 Obwq5_m obesity and body weight QTL 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141062 Obwq5_m obesity and body weight QTL 5 (mouse) qtl MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141062 Obwq5_m obesity and body weight QTL 5 (mouse) qtl MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141062 Obwq5_m obesity and body weight QTL 5 (mouse) qtl MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141062 Obwq5_m obesity and body weight QTL 5 (mouse) qtl MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141063 Ath32_m atherosclerosis 32 (mouse) qtl MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20111116 MGI PMID:17641228 4141063 Ath32_m atherosclerosis 32 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17641228 4141064 Ath37_m atherosclerosis 37 (mouse) qtl MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16624897 4141064 Ath37_m atherosclerosis 37 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16624897 4141065 Shali2_m survival time to hyperoxic acute lung injury 2 (mouse) qtl MP:0003674 oxidative stress IAGP N RGD:5509061 20111116 MGI PMID:17488888 4141065 Shali2_m survival time to hyperoxic acute lung injury 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17488888 4141067 Hbnr2_m Heligmosomoides bakeri nematode resistance 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12647241 4141067 Hbnr2_m Heligmosomoides bakeri nematode resistance 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:12647241 4141068 Modvl3_m modifier of vacuolated lens 3 (mouse) qtl MP:0001304 cataract IAGP N RGD:5509061 20111116 MGI PMID:18250320 4141068 Modvl3_m modifier of vacuolated lens 3 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18250320 4141069 Pbwg1.5_m postnatal body weight growth 1.5 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17514348 4141069 Pbwg1.5_m postnatal body weight growth 1.5 (mouse) qtl MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:17514348 4141071 Ath29_m atherosclerosis 29 (mouse) qtl MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20111116 MGI PMID:16387874 4141071 Ath29_m atherosclerosis 29 (mouse) qtl MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20111116 MGI PMID:17641228 4141071 Ath29_m atherosclerosis 29 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:17916774 4141071 Ath29_m atherosclerosis 29 (mouse) qtl MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:17916774 4141071 Ath29_m atherosclerosis 29 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16387874 4141072 Eam_m ethanol activity modifier (mouse) qtl MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20111116 MGI PMID:972950 4141072 Eam_m ethanol activity modifier (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:972950 4141073 Hpw1_m high prostate weight 1 (mouse) qtl MP:0004961 increased prostate gland weight IAGP N RGD:5509061 20111116 MGI PMID:17483418 4141073 Hpw1_m high prostate weight 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17483418 4141073 Hpw1_m high prostate weight 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17483418 4141075 Bmd1a_m bone mineral density 1a (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:16355278 4141075 Bmd1a_m bone mineral density 1a (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16355278 4141075 Bmd1a_m bone mineral density 1a (mouse) qtl MP:0003795 abnormal bone structure IAGP N RGD:5509061 20111116 MGI PMID:16355278 4141075 Bmd1a_m bone mineral density 1a (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16355278 4141075 Bmd1a_m bone mineral density 1a (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16355278 4141077 Bmrbc3_m bone marrow RBC 3 (mouse) qtl MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:17185011 4141077 Bmrbc3_m bone marrow RBC 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17185011 4141079 Ath23_m atherosclerosis 23 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16373612 4141079 Ath23_m atherosclerosis 23 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16373612 4141081 Nidd7k_m Nidd7 on KK-A (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:12115031 4141081 Nidd7k_m Nidd7 on KK-A (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115031 4141083 Wg6_m weight gain in high growth mice 6 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:17110492 4141083 Wg6_m weight gain in high growth mice 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4141085 Rbcq3_m red blood cell QTL 3 (mouse) qtl MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:16596451 4141085 Rbcq3_m red blood cell QTL 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16596451 4141086 Mvwf_m modifier of von Willebrand factor (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8986815 4141086 Mvwf_m modifier of von Willebrand factor (mouse) qtl MP:0031164 decreased circulating von Willebrand factor level IAGP N RGD:5509061 20201015 MGI PMID:8986815 4141087 Chlq4_m circulating hormone level QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12865502 4141087 Chlq4_m circulating hormone level QTL 4 (mouse) qtl MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20111116 MGI PMID:12865502 4141089 Rmp3_m resistance to mousepox 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:2002550|PMID:1433507 4141089 Rmp3_m resistance to mousepox 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20151023 MGI Created by mouse qtl pipeline PMID:2002550 4141089 Rmp3_m resistance to mousepox 3 (mouse) qtl MP:0020928 increased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:2002550 4141093 W3q17_m weight 3 weeks QTL 17 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141093 W3q17_m weight 3 weeks QTL 17 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141094 Hrtr1_m heart rate 1 (mouse) qtl MP:0002626 increased heart rate IAGP N RGD:5509061 20111116 MGI PMID:18456734 4141094 Hrtr1_m heart rate 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18456734 4141096 Asdq4_m atrial septal defect QTL 4 (mouse) qtl MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20111116 MGI PMID:16484617 4141096 Asdq4_m atrial septal defect QTL 4 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16484617 4141097 Nihls1_m noise-induced hearing loss susceptibility 1 (mouse) qtl MP:0004597 increased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20111116 MGI PMID:19337678 4141097 Nihls1_m noise-induced hearing loss susceptibility 1 (mouse) qtl MP:0005377 hearing/vestibular/ear phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19337678 4141098 Hemq2_m hematocrit QTL 2 (mouse) qtl MP:0002608 increased hematocrit IAGP N RGD:5509061 20111116 MGI PMID:16783647 4141098 Hemq2_m hematocrit QTL 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783647 4141100 Vmmt2_m vertebral morphology and mechanical traits 2 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4141100 Vmmt2_m vertebral morphology and mechanical traits 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4141101 Rv2_m Rauscher leukemia virus susceptibility 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6489477 4141101 Rv2_m Rauscher leukemia virus susceptibility 2 (mouse) qtl MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20111116 MGI PMID:6489477 4141104 Fbtq7_m femoral bone trait QTL 7 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14584885 4141104 Fbtq7_m femoral bone trait QTL 7 (mouse) qtl MP:0013615 increased volumetric bone mineral density IAGP N RGD:5509061 20220922 MGI PMID:14584885 4141107 Dmq3_m diet and mammary tumor QTL 3 (mouse) qtl MP:0001272 increased metastatic potential IAGP N RGD:5509061 20111116 MGI PMID:18288525 4141107 Dmq3_m diet and mammary tumor QTL 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18288525 4141108 Ramls2_m radiation-induced acute myeloid leukemia sensitivity 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12411293 4141108 Ramls2_m radiation-induced acute myeloid leukemia sensitivity 2 (mouse) qtl MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20111116 MGI PMID:12411293 4141109 Tgq6_m triglyceride QTL 6 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4141109 Tgq6_m triglyceride QTL 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4141111 Abshq1_m abnormal sperm head QTL 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18689897 4141111 Abshq1_m abnormal sperm head QTL 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18689897 4141111 Abshq1_m abnormal sperm head QTL 1 (mouse) qtl MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20111116 MGI PMID:18689897 4141112 Tglq2a_m triglyceride QTL 2a (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17496333 4141113 Tgq28_m triglyceride QTL 28 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4141113 Tgq28_m triglyceride QTL 28 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4141114 Ascla2_m atherosclerotic lesion area 2 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16380418 4141114 Ascla2_m atherosclerotic lesion area 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16380418 4141115 Albq7_m albuminuria QTL 7 (mouse) qtl MP:0002871 albuminuria IAGP N RGD:5509061 20111116 MGI PMID:17804484 4141115 Albq7_m albuminuria QTL 7 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17804484 4141115 Albq7_m albuminuria QTL 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17804484 4141116 Lgaq4_m late growth adjusted QTL 4 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141116 Lgaq4_m late growth adjusted QTL 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141117 Drinksac3_m drink saccharin 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141117 Drinksac3_m drink saccharin 3 (mouse) qtl MP:0011941 increased fluid intake IAGP N RGD:5509061 20130503 MGI PMID:18363849 4141119 Rv3_m Rauscher leukemia virus susceptibility 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6489477 4141119 Rv3_m Rauscher leukemia virus susceptibility 3 (mouse) qtl MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20111116 MGI PMID:6489477 4141122 Chlq5_m circulating hormone level QTL 5 (mouse) qtl MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:16782841 4141122 Chlq5_m circulating hormone level QTL 5 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:12865502 4141122 Chlq5_m circulating hormone level QTL 5 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:16782841 4141122 Chlq5_m circulating hormone level QTL 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12865502 4141123 Vmmt1_m vertebral morphology and mechanical traits 1 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4141123 Vmmt1_m vertebral morphology and mechanical traits 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4141127 W3q4_m weight 3 weeks QTL 4 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141127 W3q4_m weight 3 weeks QTL 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141128 Mdmg1_m mandibular morphogenesis 1 (mouse) qtl MP:0004595 abnormal mandibular condyloid process morphology IEA N RGD:5509061 20111116 MGI 4141128 Mdmg1_m mandibular morphogenesis 1 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 4141128 Mdmg1_m mandibular morphogenesis 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 4141131 Ril3_m radiation-induced leukemia sensitivity 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6270228 4141131 Ril3_m radiation-induced leukemia sensitivity 3 (mouse) qtl MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20111116 MGI PMID:6270228 4141131 Ril3_m radiation-induced leukemia sensitivity 3 (mouse) qtl MP:0004503 decreased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20111116 MGI PMID:6270228 4141132 Eae18_m experimental allergic encephalomyelitis susceptibility 18 (mouse) qtl MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20111116 MGI PMID:7561115 4141132 Eae18_m experimental allergic encephalomyelitis susceptibility 18 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7561115 4141134 Eac6_m ethyl alcohol consumption QTL 6 (mouse) qtl MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:17273929 4141134 Eac6_m ethyl alcohol consumption QTL 6 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17273929 4141135 Cia35_m collagen induced arthritis 35 (mouse) qtl MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17312155 4141135 Cia35_m collagen induced arthritis 35 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17312155 4141135 Cia35_m collagen induced arthritis 35 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:17312155 4141135 Cia35_m collagen induced arthritis 35 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17312155 4141135 Cia35_m collagen induced arthritis 35 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17312155 4141136 Boneq_m bone trait QTL (mouse) qtl MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:18239664 4141136 Boneq_m bone trait QTL (mouse) qtl MP:0003795 abnormal bone structure IAGP N RGD:5509061 20111215 MGI PMID:18239664 4141136 Boneq_m bone trait QTL (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18239664 4141137 Tcq1_m total cholesterol QTL 1 (mouse) qtl MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:17110492 4141137 Tcq1_m total cholesterol QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4141139 Hmtb4_m hemostasis and thrombosis rebleeding time 4 (mouse) qtl MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20111116 MGI PMID:18787898 4141139 Hmtb4_m hemostasis and thrombosis rebleeding time 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18787898 4141141 Mcr_m mast cell regulator (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:3610252 4141141 Mcr_m mast cell regulator (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:3610252 4141141 Mcr_m mast cell regulator (mouse) qtl MP:0031395 cutaneous mastocytosis IAGP N RGD:5509061 20220721 MGI PMID:3610252 4141142 Ath2_m atherosclerosis 2 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:2499515 4141142 Ath2_m atherosclerosis 2 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:2499515 4141142 Ath2_m atherosclerosis 2 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:2499515 4141142 Ath2_m atherosclerosis 2 (mouse) qtl MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:2499515 4141142 Ath2_m atherosclerosis 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:2499515 4141142 Ath2_m atherosclerosis 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:2499515 4141148 Cq5_m cholesterol QTL 5 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14974682 4141148 Cq5_m cholesterol QTL 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14974682 4141149 Hbnr4_m Heligmosomoides bakeri nematode resistance 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14507332 4141150 Raml1_m radiation induced acute myeloid leukemia 1 (mouse) qtl MP:0002879 increased cellular sensitivity to X-ray irradiation IAGP N RGD:5509061 20111116 MGI PMID:16093251 4141150 Raml1_m radiation induced acute myeloid leukemia 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16093251 4141151 Ath38_m atherosclerosis 38 (mouse) qtl MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16624897 4141151 Ath38_m atherosclerosis 38 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16624897 4141152 Spw5_m spleen weight 5 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:18552208 4141152 Spw5_m spleen weight 5 (mouse) qtl MP:0004953 decreased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:18552208 4141152 Spw5_m spleen weight 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18552208 4141152 Spw5_m spleen weight 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141152 Spw5_m spleen weight 5 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141154 Nba1_m New Zealand Black autoimmunity 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11739537 4141154 Nba1_m New Zealand Black autoimmunity 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11739537 4141155 Plast2b_m plasma plant sterol 2b (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12446833 4141155 Plast2b_m plasma plant sterol 2b (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12446833 4141158 Wg5_m weight gain in high growth mice 5 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:17110492 4141158 Wg5_m weight gain in high growth mice 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4141158 Wg5_m weight gain in high growth mice 5 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4141159 Phl2_m progressive hearing loss 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16897347 4141159 Phl2_m progressive hearing loss 2 (mouse) qtl MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20111116 MGI PMID:16897347 4141159 Phl2_m progressive hearing loss 2 (mouse) qtl MP:0004767 increased cochlear nerve compound action potential IAGP N RGD:5509061 20111116 MGI PMID:16897347 4141159 Phl2_m progressive hearing loss 2 (mouse) qtl MP:0005377 hearing/vestibular/ear phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16897347 4141160 Cq1_m cholesterol QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10101257 4141161 Lch2_m low cholesterol 2 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20130704 MGI PMID:12420138 4141161 Lch2_m low cholesterol 2 (mouse) qtl MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20130704 MGI PMID:12420138 4141161 Lch2_m low cholesterol 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 4141162 Mleu4_m myeloid leukemia survival 4 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141162 Mleu4_m myeloid leukemia survival 4 (mouse) qtl MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20111116 MGI PMID:18552208 4141163 Hypn3_m hyperinsulinemia 3 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:15561960 4141163 Hypn3_m hyperinsulinemia 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561960 4141164 Egq3_m early growth QTL 3 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141164 Egq3_m early growth QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141165 Bglu3_m blood glucose level 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16595606 4141165 Bglu3_m blood glucose level 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16595606 4141165 Bglu3_m blood glucose level 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16595606 4141165 Bglu3_m blood glucose level 3 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:16595606 4141166 Appd1_m APP associated premature death 1 (mouse) qtl MP:0002083 premature death IAGP N RGD:5509061 20111116 MGI PMID:15254013 4141166 Appd1_m APP associated premature death 1 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15254013 4141167 Lpn2_m NZ lupus nephritis 2 (mouse) qtl MP:0001859 kidney inflammation IAGP N RGD:5509061 20111116 MGI PMID:681876 4141167 Lpn2_m NZ lupus nephritis 2 (mouse) qtl MP:0002962 increased urine protein level IAGP N RGD:5509061 20111116 MGI PMID:681876 4141167 Lpn2_m NZ lupus nephritis 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:681876 4141167 Lpn2_m NZ lupus nephritis 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:681876 4141167 Lpn2_m NZ lupus nephritis 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:681876 4141168 Secia6_m small effect CIA locus 6 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17244351 4141168 Secia6_m small effect CIA locus 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4141168 Secia6_m small effect CIA locus 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4141169 Pbft3_m percent body fat 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17179051 4141169 Pbft3_m percent body fat 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:17179051 4141169 Pbft3_m percent body fat 3 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:17179051 4141170 Ua1_m urinary albuminuria 1 (mouse) qtl MP:0002871 albuminuria IAGP N RGD:5509061 20111116 MGI PMID:15769825 4141170 Ua1_m urinary albuminuria 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15769825 4141170 Ua1_m urinary albuminuria 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15769825 4141172 W6q9_m weight 6 weeks QTL 9 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141172 W6q9_m weight 6 weeks QTL 9 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141173 Bmrbc4_m bone marrow RBC 4 (mouse) qtl MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:17185011 4141173 Bmrbc4_m bone marrow RBC 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17185011 4141174 Brwt2_m brain weight 2 (mouse) qtl MP:0002176 increased brain weight IAGP N RGD:5509061 20111116 MGI PMID:1393606 4141174 Brwt2_m brain weight 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1393606 4141175 Drinkkcl3_m drink potassium chloride 3 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4141175 Drinkkcl3_m drink potassium chloride 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141178 Ffaq3_m free fatty acid QTL 3 (mouse) qtl MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4141178 Ffaq3_m free fatty acid QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4141180 Ssic1_m susceptibility to small intestinal cancer 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7606739 4141180 Ssic1_m susceptibility to small intestinal cancer 1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:7606739 4141180 Ssic1_m susceptibility to small intestinal cancer 1 (mouse) qtl MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20150326 MGI PMID:7606739 4141181 Char9_m P. chabaudi malaria resistance QTL 9 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:17312006 4141181 Char9_m P. chabaudi malaria resistance QTL 9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17312006 4141182 Mcvq3_m mean corpuscular volume QTL 3 (mouse) qtl MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20111116 MGI PMID:16596451 4141182 Mcvq3_m mean corpuscular volume QTL 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16596451 4141184 Tb2r1_m TGF-beta2 responsiveness 1 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:14707111 4141184 Tb2r1_m TGF-beta2 responsiveness 1 (mouse) qtl MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20111116 MGI PMID:18941179 4141184 Tb2r1_m TGF-beta2 responsiveness 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14707111 4141185 Nicoq1_m nicotine consumption QTL 1 (mouse) qtl MP:0002553 preference for addictive substance IAGP N RGD:5509061 20111116 MGI PMID:17010155 4141185 Nicoq1_m nicotine consumption QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17010155 4141186 Pbwg1.8_m postnatal body weight growth 1.8 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17514348 4141186 Pbwg1.8_m postnatal body weight growth 1.8 (mouse) qtl MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:17514348 4141188 Tgq7_m triglyceride QTL 7 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4141188 Tgq7_m triglyceride QTL 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4141191 Amdt1_m amphetamine distance traveled 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16710777 4141191 Amdt1_m amphetamine distance traveled 1 (mouse) qtl MP:0008911 induced hyperactivity IAGP N RGD:5509061 20220421 MGI PMID:16710777 4141192 Ssrq2_m stress response QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17913702 4141192 Ssrq2_m stress response QTL 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17913702 4141192 Ssrq2_m stress response QTL 2 (mouse) qtl MP:0010166 increased response to stress-induced hyperthermia IAGP N RGD:5509061 20111116 MGI PMID:17913702 4141193 Hfgi1_m Helicobacter felis gastric inflammation 1 (mouse) qtl MP:0001873 stomach inflammation IAGP N RGD:5509061 20111116 MGI PMID:17474149 4141193 Hfgi1_m Helicobacter felis gastric inflammation 1 (mouse) qtl MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20111116 MGI PMID:17474149 4141193 Hfgi1_m Helicobacter felis gastric inflammation 1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17474149 4141193 Hfgi1_m Helicobacter felis gastric inflammation 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17474149 4141193 Hfgi1_m Helicobacter felis gastric inflammation 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17474149 4141193 Hfgi1_m Helicobacter felis gastric inflammation 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17474149 4141195 Nilac11_m nicotine induced locomotor activity 11 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16176386 4141195 Nilac11_m nicotine induced locomotor activity 11 (mouse) qtl MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:16176386 4141195 Nilac11_m nicotine induced locomotor activity 11 (mouse) qtl MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:19083055 4141196 Lynf4_m lymphocyte infiltration 4 (mouse) qtl MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20111116 MGI PMID:17703301 4141196 Lynf4_m lymphocyte infiltration 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17703301 4141198 Nilac7_m nicotine induced locomotor activity 7 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16176386 4141198 Nilac7_m nicotine induced locomotor activity 7 (mouse) qtl MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:16176386 4141199 Bwtq10_m body weight QTL 10 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141199 Bwtq10_m body weight QTL 10 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141200 Fbtq8_m femoral bone trait QTL 8 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:14584885 4141200 Fbtq8_m femoral bone trait QTL 8 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14584885 4141200 Fbtq8_m femoral bone trait QTL 8 (mouse) qtl MP:0013615 increased volumetric bone mineral density IAGP N RGD:5509061 20220922 MGI PMID:14584885 4141200 Fbtq8_m femoral bone trait QTL 8 (mouse) qtl MP:0013637 increased femur stiffness IAGP N RGD:5509061 20220922 MGI PMID:14584885 4141203 Lbca1_m LPS-induced B cell activation 1 (mouse) qtl MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:16982900 4141203 Lbca1_m LPS-induced B cell activation 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16982900 4141203 Lbca1_m LPS-induced B cell activation 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16982900 4141203 Lbca1_m LPS-induced B cell activation 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16982900 4141203 Lbca1_m LPS-induced B cell activation 1 (mouse) qtl MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20111116 MGI PMID:16982900 4141205 Bmd5a_m bone mineral density 5a (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20220916 MGI Created by mouse qtl pipeline PMID:17451375 4141205 Bmd5a_m bone mineral density 5a (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17451375 4141205 Bmd5a_m bone mineral density 5a (mouse) qtl MP:0010875 increased bone volume IAGP N RGD:5509061 20220922 MGI PMID:17451375 4141205 Bmd5a_m bone mineral density 5a (mouse) qtl MP:0013623 increased femur compact bone thickness IAGP N RGD:5509061 20220915 MGI PMID:17451375 4141205 Bmd5a_m bone mineral density 5a (mouse) qtl MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20220915 MGI PMID:17451375 4141205 Bmd5a_m bone mineral density 5a (mouse) qtl MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:17451375 4141205 Bmd5a_m bone mineral density 5a (mouse) qtl MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:17451375 4141206 Mcdq1_m molar crown diameter QTL 1 (mouse) qtl MP:0003932 abnormal molar crown morphology IAGP N RGD:5509061 20111116 MGI PMID:14691112 4141206 Mcdq1_m molar crown diameter QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:14691112 4141206 Mcdq1_m molar crown diameter QTL 1 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14691112 4141206 Mcdq1_m molar crown diameter QTL 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:14691112 4141207 Imrfq1_m immune response to Factor IX QTL 1 (mouse) qtl MP:0002493 increased IgG level IAGP N RGD:5509061 20111116 MGI PMID:15922957 4141207 Imrfq1_m immune response to Factor IX QTL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15922957 4141207 Imrfq1_m immune response to Factor IX QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15922957 4141208 Bglu8_m blood glucose level 8 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4141208 Bglu8_m blood glucose level 8 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4141210 Ascla3_m atherosclerotic lesion area 3 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16380418 4141210 Ascla3_m atherosclerotic lesion area 3 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16380418 4141211 Lus_m lymphoid cytostasis suppressor (mouse) qtl MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20111116 MGI PMID:6228526 4141211 Lus_m lymphoid cytostasis suppressor (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:108205|PMID:6228526 4141212 Imraq3_m immune response to AAV2 QTL 3 (mouse) qtl MP:0002493 increased IgG level IAGP N RGD:5509061 20111116 MGI PMID:15922957 4141212 Imraq3_m immune response to AAV2 QTL 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15922957 4141212 Imraq3_m immune response to AAV2 QTL 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15922957 4141213 Mmom3_m mammary modifier of Min 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18056448 4141213 Mmom3_m mammary modifier of Min 3 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18056448 4141213 Mmom3_m mammary modifier of Min 3 (mouse) qtl MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:18056448 4141213 Mmom3_m mammary modifier of Min 3 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18056448 4141215 Mnic1_m macronutrient intake, carbohydrate 1 (mouse) qtl MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20111116 MGI PMID:12388789 4141215 Mnic1_m macronutrient intake, carbohydrate 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12388789 4141215 Mnic1_m macronutrient intake, carbohydrate 1 (mouse) qtl MP:0011939 increased food intake IAGP N RGD:5509061 20130322 MGI PMID:16946080 4141216 Idd16.1_m insulin dependent diabetes susceptibility 16.1 (mouse) qtl MP:0001869 pancreas inflammation IAGP N RGD:5509061 20111116 MGI PMID:15855353 4141216 Idd16.1_m insulin dependent diabetes susceptibility 16.1 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:15855353 4141216 Idd16.1_m insulin dependent diabetes susceptibility 16.1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15855353 4141216 Idd16.1_m insulin dependent diabetes susceptibility 16.1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15855353 4141216 Idd16.1_m insulin dependent diabetes susceptibility 16.1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15855353 4141218 Ath24_m atherosclerosis 24 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16373612 4141218 Ath24_m atherosclerosis 24 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16373612 4141219 W10q16_m weight 10 weeks QTL 16 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141219 W10q16_m weight 10 weeks QTL 16 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141220 Cia22_m collagen induced arthritis 22 (mouse) qtl MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:15716976 4141220 Cia22_m collagen induced arthritis 22 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15716976 4141220 Cia22_m collagen induced arthritis 22 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15716976 4141222 Hdlq60_m HDL QTL 60 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18772481 4141222 Hdlq60_m HDL QTL 60 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18772481 4141223 Secia7_m small effect CIA locus 7 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17244351 4141223 Secia7_m small effect CIA locus 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4141223 Secia7_m small effect CIA locus 7 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4141224 Dxmod_m doxorubicin nephropathy modifier (mouse) qtl MP:0002705 dilated renal tubule IAGP N RGD:5509061 20111116 MGI PMID:15699352 4141224 Dxmod_m doxorubicin nephropathy modifier (mouse) qtl MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20111116 MGI PMID:15699352 4141224 Dxmod_m doxorubicin nephropathy modifier (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15699352 4141225 Adip14_m adiposity 14 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141225 Adip14_m adiposity 14 (mouse) qtl MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141226 Wg2b_m weight gain in high growth mice 2b (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:17694346 4141226 Wg2b_m weight gain in high growth mice 2b (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17694346 4141226 Wg2b_m weight gain in high growth mice 2b (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17694346 4141226 Wg2b_m weight gain in high growth mice 2b (mouse) qtl MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:17694346 4141227 Smtw1_m small testis weight 1 (mouse) qtl MP:0004852 decreased testis weight IAGP N RGD:5509061 20111116 MGI PMID:16651692 4141227 Smtw1_m small testis weight 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16651692 4141227 Smtw1_m small testis weight 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16651692 4141228 Pbat1_m platelet-binding antibody-associated thrombocytopenia 1 (mouse) qtl MP:0003179 thrombocytopenia IAGP N RGD:5509061 20111116 MGI PMID:9754557 4141228 Pbat1_m platelet-binding antibody-associated thrombocytopenia 1 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:9754557 4141228 Pbat1_m platelet-binding antibody-associated thrombocytopenia 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9754557 4141228 Pbat1_m platelet-binding antibody-associated thrombocytopenia 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9754557 4141229 Sfp3_m short free-running period 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19173005 4141229 Sfp3_m short free-running period 3 (mouse) qtl MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:19173005 4141230 Afteq2_m acute functional tolerance to ethanol QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17250610 4141230 Afteq2_m acute functional tolerance to ethanol QTL 2 (mouse) qtl MP:0005443 abnormal ethanol metabolism IAGP N RGD:5509061 20111116 MGI PMID:17250610 4141231 Hdlq40_m HDL QTL 40 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16951076 4141231 Hdlq40_m HDL QTL 40 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16951076 4141232 Cxv2_m control of xenotropic virus 2 (mouse) qtl MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20111116 MGI PMID:221612 4141232 Cxv2_m control of xenotropic virus 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:221612 4141234 Pbwg14_m postnatal body weight growth 14 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 4141234 Pbwg14_m postnatal body weight growth 14 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16174331 4141236 Hbnr5_m Heligmosomoides bakeri nematode resistance 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14507332 4141237 Plbcq1_m pleiotropic body composition QTL 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:18286334 4141237 Plbcq1_m pleiotropic body composition QTL 1 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:18286334 4141237 Plbcq1_m pleiotropic body composition QTL 1 (mouse) qtl MP:0003960 increased lean body mass IAGP N RGD:5509061 20111116 MGI PMID:18286334 4141237 Plbcq1_m pleiotropic body composition QTL 1 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18286334 4141237 Plbcq1_m pleiotropic body composition QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18286334 4141239 Brwt3_m brain weight 3 (mouse) qtl MP:0002176 increased brain weight IAGP N RGD:5509061 20111116 MGI PMID:1393606 4141239 Brwt3_m brain weight 3 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1393606 4141240 Mlca4_m modifier of locomotor activity 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16436185 4141240 Mlca4_m modifier of locomotor activity 4 (mouse) qtl MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:16436185 4141241 Find1_m fat induced diabetes 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15870393 4141241 Find1_m fat induced diabetes 1 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:15870393 4141242 Psrs2_m psoriasis susceptibility 2 (mouse) qtl MP:0001193 psoriasis IAGP N RGD:5509061 20111116 MGI PMID:16982899 4141242 Psrs2_m psoriasis susceptibility 2 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16982899 4141243 Tgq8_m triglyceride QTL 8 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4141243 Tgq8_m triglyceride QTL 8 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4141244 Bmd5c_m bone mineral density 5c (mouse) qtl MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20111116 MGI PMID:17451375 4141244 Bmd5c_m bone mineral density 5c (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17451375 4141245 Cq2_m cholesterol QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10101257 4141248 Rmp1_m resistance to mousepox (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7637035 4141248 Rmp1_m resistance to mousepox (mouse) qtl MP:0020928 increased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:7637035 4141249 Brnwq_m brain weight QTL (mouse) qtl MP:0002175 decreased brain weight IAGP N RGD:5509061 20111116 MGI PMID:18239664 4141249 Brnwq_m brain weight QTL (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18239664 4141250 Arrh1_m arrhythmicity 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19173005 4141250 Arrh1_m arrhythmicity 1 (mouse) qtl MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:19173005 4141251 Secia5_m small effect CIA locus 5 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17244351 4141251 Secia5_m small effect CIA locus 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4141251 Secia5_m small effect CIA locus 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4141252 Modvl2_m modifier of vacuolated lens 2 (mouse) qtl MP:0003054 spina bifida IAGP N RGD:5509061 20111116 MGI PMID:18250320 4141252 Modvl2_m modifier of vacuolated lens 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18250320 4141252 Modvl2_m modifier of vacuolated lens 2 (mouse) qtl MP:0005380 embryo phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18250320 4141253 Brabq2_m brain amyloid beta QTL 2 (mouse) qtl MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20111116 MGI PMID:17400334 4141253 Brabq2_m brain amyloid beta QTL 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17400334 4141253 Brabq2_m brain amyloid beta QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20140718 MGI Created by mouse qtl pipeline PMID:17400334 4141253 Brabq2_m brain amyloid beta QTL 2 (mouse) qtl MP:0005395 obsolete other phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17400334 4141254 Plast1b_m plasma plant sterol 1b (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16840795 4141254 Plast1b_m plasma plant sterol 1b (mouse) qtl MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20111116 MGI PMID:16840795 4141254 Plast1b_m plasma plant sterol 1b (mouse) qtl MP:0003192 increased cholesterol efflux IAGP N RGD:5509061 20111116 MGI PMID:16840795 4141254 Plast1b_m plasma plant sterol 1b (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16840795 4141254 Plast1b_m plasma plant sterol 1b (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16840795 4141254 Plast1b_m plasma plant sterol 1b (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16840795 4141255 W10q3_m weight 10 weeks QTL 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141255 W10q3_m weight 10 weeks QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141257 Miju_m modifier of IgJ upregulation (mouse) qtl MP:0002495 increased IgA level IAGP N RGD:5509061 20111116 MGI PMID:15175647 4141257 Miju_m modifier of IgJ upregulation (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15175647 4141257 Miju_m modifier of IgJ upregulation (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15175647 4141260 Actre6_m activity response to ethanol 6 (mouse) qtl MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20111116 MGI PMID:17143586 4141260 Actre6_m activity response to ethanol 6 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17143586 4141262 Pis2_m pilocarpine-induced seizures 2 (mouse) qtl MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20111116 MGI PMID:17242861 4141262 Pis2_m pilocarpine-induced seizures 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17242861 4141262 Pis2_m pilocarpine-induced seizures 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17242861 4141263 Lch_m low cholesterol (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20130704 MGI PMID:12420138 4141263 Lch_m low cholesterol (mouse) qtl MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20130704 MGI PMID:12420138 4141263 Lch_m low cholesterol (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline 4141264 Qbis3_m QTL for body weight independent of sex 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16321990 4141264 Qbis3_m QTL for body weight independent of sex 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16321990 4141265 Appd2_m APP associated premature death 2 (mouse) qtl MP:0002083 premature death IAGP N RGD:5509061 20111116 MGI PMID:15254013 4141265 Appd2_m APP associated premature death 2 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15254013 4141267 Nicoq2_m nicotine consumption QTL 2 (mouse) qtl MP:0002553 preference for addictive substance IAGP N RGD:5509061 20111116 MGI PMID:17010155 4141267 Nicoq2_m nicotine consumption QTL 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17010155 4141270 Swqnd1_m spleen weight QTL 1 (mouse) qtl MP:0004953 decreased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141270 Swqnd1_m spleen weight QTL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4141270 Swqnd1_m spleen weight QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4141271 Why2_m wild-derived hyperresponse 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18268037 4141271 Why2_m wild-derived hyperresponse 2 (mouse) qtl MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20111116 MGI PMID:18268037 4141272 Tfv1_m total food volume 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18077508 4141272 Tfv1_m total food volume 1 (mouse) qtl MP:0005449 abnormal food intake IAGP N RGD:5509061 20111116 MGI PMID:18077508 4141273 Drinksac1_m drink saccharin 1 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20130503 MGI PMID:18363849 4141273 Drinksac1_m drink saccharin 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141273 Drinksac1_m drink saccharin 1 (mouse) qtl MP:0011941 increased fluid intake IAGP N RGD:5509061 20130503 MGI PMID:18363849 4141276 Drinkkcl4_m drink potassium chloride 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141276 Drinkkcl4_m drink potassium chloride 4 (mouse) qtl MP:0011941 increased fluid intake IAGP N RGD:5509061 20130503 MGI PMID:18363849 4141277 Ath33_m atherosclerosis 33 (mouse) qtl MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20111116 MGI PMID:17641228 4141277 Ath33_m atherosclerosis 33 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17641228 4141279 Hdlq51_m HDL QTL 51 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16951076 4141279 Hdlq51_m HDL QTL 51 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16951076 4141281 Ssrq1_m stress response QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17913702 4141281 Ssrq1_m stress response QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17913702 4141281 Ssrq1_m stress response QTL 1 (mouse) qtl MP:0010166 increased response to stress-induced hyperthermia IAGP N RGD:5509061 20111116 MGI PMID:17913702 4141282 Bwtq9_m body weight QTL 9 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141282 Bwtq9_m body weight QTL 9 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141283 Amdt2_m amphetamine distance traveled 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16710777 4141283 Amdt2_m amphetamine distance traveled 2 (mouse) qtl MP:0008911 induced hyperactivity IAGP N RGD:5509061 20220421 MGI PMID:16710777 4141285 Tgq18_m triglyceride QTL 18 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4141285 Tgq18_m triglyceride QTL 18 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4141287 Bmd20_m bone mineral density 20 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:16355279 4141287 Bmd20_m bone mineral density 20 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16355279 4141287 Bmd20_m bone mineral density 20 (mouse) qtl MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20220922 MGI PMID:16355279 4141289 Sox10m2_m Sox10Dom modifier 2 (mouse) qtl MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20111116 MGI PMID:17028340 4141289 Sox10m2_m Sox10Dom modifier 2 (mouse) qtl MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20111116 MGI PMID:15843399 4141289 Sox10m2_m Sox10Dom modifier 2 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15843399 4141292 Ril1_m radiation-induced leukemia sensitivity 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6270228|PMID:6300845 4141292 Ril1_m radiation-induced leukemia sensitivity 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20151113 MGI Created by mouse qtl pipeline PMID:6270228 4141292 Ril1_m radiation-induced leukemia sensitivity 1 (mouse) qtl MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20111116 MGI PMID:6270228 4141292 Ril1_m radiation-induced leukemia sensitivity 1 (mouse) qtl MP:0004503 decreased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20111116 MGI PMID:6270228 4141293 Gluchos3_m glucose homeostasis QTL 3 (mouse) qtl MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:15729571 4141293 Gluchos3_m glucose homeostasis QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15729571 4141297 Plyid_m Polymeric IgA dominance (mouse) qtl MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20111116 MGI PMID:15259017 4141297 Plyid_m Polymeric IgA dominance (mouse) qtl MP:0002495 increased IgA level IAGP N RGD:5509061 20111116 MGI PMID:15259017 4141297 Plyid_m Polymeric IgA dominance (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15259017 4141297 Plyid_m Polymeric IgA dominance (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15259017 4141298 Bdwtq_m body weight QTL (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:18239664 4141298 Bdwtq_m body weight QTL (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:18239664 4141298 Bdwtq_m body weight QTL (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18239664 4141298 Bdwtq_m body weight QTL (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18239664 4141298 Bdwtq_m body weight QTL (mouse) qtl MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:18239664 4141298 Bdwtq_m body weight QTL (mouse) qtl MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:18239664 4141298 Bdwtq_m body weight QTL (mouse) qtl MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:18239664 4141298 Bdwtq_m body weight QTL (mouse) qtl MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:18239664 4141299 Ascla4_m atherosclerotic lesion area 4 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16380418 4141299 Ascla4_m atherosclerotic lesion area 4 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16380418 4141300 Asdq6_m atrial septal defect QTL 6 (mouse) qtl MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20111116 MGI PMID:16484617 4141300 Asdq6_m atrial septal defect QTL 6 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16484617 4141302 Ssrq5_m stress response QTL 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17913702 4141302 Ssrq5_m stress response QTL 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17913702 4141302 Ssrq5_m stress response QTL 5 (mouse) qtl MP:0010166 increased response to stress-induced hyperthermia IAGP N RGD:5509061 20111116 MGI PMID:17913702 4141303 Hemq6_m hematocrit QTL 6 (mouse) qtl MP:0002608 increased hematocrit IAGP N RGD:5509061 20111116 MGI PMID:16783647 4141303 Hemq6_m hematocrit QTL 6 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783647 4141305 Tgq9_m triglyceride QTL 9 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4141305 Tgq9_m triglyceride QTL 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4141306 Tmrb2_m trace metal regulation in brain 2 (mouse) qtl MP:0000192 abnormal mineral level IAGP N RGD:5509061 20111116 MGI PMID:18189309 4141306 Tmrb2_m trace metal regulation in brain 2 (mouse) qtl MP:0003952 abnormal copper level IAGP N RGD:5509061 20111116 MGI PMID:18189309 4141306 Tmrb2_m trace metal regulation in brain 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18189309 4141308 Secia8_m small effect CIA locus 8 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17244351 4141308 Secia8_m small effect CIA locus 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4141308 Secia8_m small effect CIA locus 8 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4141312 Cia21_m collagen induced arthritis 21 (mouse) qtl MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:15716976 4141312 Cia21_m collagen induced arthritis 21 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15716976 4141312 Cia21_m collagen induced arthritis 21 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15716976 4141319 Hmtb8_m hemostasis and thrombosis rebleeding time 8 (mouse) qtl MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20111116 MGI PMID:18787898 4141319 Hmtb8_m hemostasis and thrombosis rebleeding time 8 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18787898 4141321 Afteq1_m acute functional tolerance to ethanol QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17250610 4141321 Afteq1_m acute functional tolerance to ethanol QTL 1 (mouse) qtl MP:0005443 abnormal ethanol metabolism IAGP N RGD:5509061 20111116 MGI PMID:17250610 4141322 Pitgp_m Pecam1-independent thioglycollate peritonitis (mouse) qtl MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20111116 MGI PMID:19180231 4141322 Pitgp_m Pecam1-independent thioglycollate peritonitis (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19180231 4141322 Pitgp_m Pecam1-independent thioglycollate peritonitis (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19180231 4141323 Ptnu3_m proteinuria 3 (mouse) qtl MP:0002962 increased urine protein level IAGP N RGD:5509061 20111116 MGI PMID:15965785 4141323 Ptnu3_m proteinuria 3 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15965785 4141323 Ptnu3_m proteinuria 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15965785 4141325 Mom7_m modifier of Min 7 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17435219 4141325 Mom7_m modifier of Min 7 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17435219 4141325 Mom7_m modifier of Min 7 (mouse) qtl MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:17435219 4141326 Mtgq5_m multiple trait growth QTL 5 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15457339 4141326 Mtgq5_m multiple trait growth QTL 5 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141326 Mtgq5_m multiple trait growth QTL 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 4141329 Mleu1_m myeloid leukemia survival 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141329 Mleu1_m myeloid leukemia survival 1 (mouse) qtl MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20111116 MGI PMID:18552208 4141330 Iva1_m isovaleric acid smelling 1 (mouse) qtl MP:0001984 abnormal olfaction IAGP N RGD:5509061 20111116 MGI PMID:8521470 4141330 Iva1_m isovaleric acid smelling 1 (mouse) qtl MP:0005394 taste/olfaction phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8521470 4141331 Cplaq11_m circadian period of locomotor activity 11 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14667146 4141331 Cplaq11_m circadian period of locomotor activity 11 (mouse) qtl MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:14667146 4141334 Lctlp2_m lymph node cytotoxic T lymphocyte percentage 2 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17361202 4141334 Lctlp2_m lymph node cytotoxic T lymphocyte percentage 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17361202 4141334 Lctlp2_m lymph node cytotoxic T lymphocyte percentage 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17361202 4141334 Lctlp2_m lymph node cytotoxic T lymphocyte percentage 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17361202 4141334 Lctlp2_m lymph node cytotoxic T lymphocyte percentage 2 (mouse) qtl MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20111116 MGI PMID:17361202 4141335 W6q10_m weight 6 weeks QTL 10 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141335 W6q10_m weight 6 weeks QTL 10 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141336 Exa_m exploratory activity (mouse) qtl MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20111116 MGI PMID:4715816 4141336 Exa_m exploratory activity (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:4715816 4141337 Why1_m wild-derived hyperresponse 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18268037 4141337 Why1_m wild-derived hyperresponse 1 (mouse) qtl MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20111116 MGI PMID:18268037 4141339 Nilac2_m nicotine induced locomotor activity 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16176386 4141339 Nilac2_m nicotine induced locomotor activity 2 (mouse) qtl MP:0009756 impaired behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:16176386 4141340 ahl4_m age related hearing loss 4 (mouse) qtl MP:0005377 hearing/vestibular/ear phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18280008 4141344 Hdlq49_m HDL QTL 49 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16951076 4141344 Hdlq49_m HDL QTL 49 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16951076 4141345 Lynf2_m lymphocyte infiltration 2 (mouse) qtl MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20111116 MGI PMID:17703301 4141345 Lynf2_m lymphocyte infiltration 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17703301 4141346 Skmw12_m skeletal muscle weight 12 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783642 4141346 Skmw12_m skeletal muscle weight 12 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16783642 4141346 Skmw12_m skeletal muscle weight 12 (mouse) qtl MP:0009421 increased gastrocnemius weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 4141348 Fbtq2_m femoral bone trait QTL 2 (mouse) qtl MP:0003795 abnormal bone structure IAGP N RGD:5509061 20111116 MGI PMID:14584885 4141348 Fbtq2_m femoral bone trait QTL 2 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:14584885 4141348 Fbtq2_m femoral bone trait QTL 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14584885 4141348 Fbtq2_m femoral bone trait QTL 2 (mouse) qtl MP:0013615 increased volumetric bone mineral density IAGP N RGD:5509061 20220922 MGI PMID:14584885 4141348 Fbtq2_m femoral bone trait QTL 2 (mouse) qtl MP:0013637 increased femur stiffness IAGP N RGD:5509061 20220922 MGI PMID:14584885 4141349 Dmq2_m diet and mammary tumor QTL 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18288525 4141349 Dmq2_m diet and mammary tumor QTL 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18288525 4141349 Dmq2_m diet and mammary tumor QTL 2 (mouse) qtl MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:18288525 4141349 Dmq2_m diet and mammary tumor QTL 2 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18288525 4141350 Bnszq2_m bone size QTL 2 (mouse) qtl MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20111116 MGI PMID:15883645 4141350 Bnszq2_m bone size QTL 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15883645 4141351 Elda4_m ethanol induced low dose activation 4 (mouse) qtl MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20111116 MGI PMID:16792557 4141351 Elda4_m ethanol induced low dose activation 4 (mouse) qtl MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20111116 MGI PMID:16792557 4141351 Elda4_m ethanol induced low dose activation 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16792557 4141352 Qbis2_m QTL for body weight independent of sex 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16321990 4141352 Qbis2_m QTL for body weight independent of sex 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16321990 4141352 Qbis2_m QTL for body weight independent of sex 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16321990 4141352 Qbis2_m QTL for body weight independent of sex 2 (mouse) qtl MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16321990 4141353 Earheal1_m ear healing QTL 1 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:16208538 4141353 Earheal1_m ear healing QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16208538 4141356 Hdlq59_m HDL QTL 59 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18772481 4141356 Hdlq59_m HDL QTL 59 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18772481 4141357 Mrdq1_m modifier of retinal degeneration QTL 1 (mouse) qtl MP:0001326 retina degeneration IAGP N RGD:5509061 20111116 MGI PMID:18344445 4141357 Mrdq1_m modifier of retinal degeneration QTL 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18344445 4141358 Ath22_m atherosclerosis 22 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16373612 4141358 Ath22_m atherosclerosis 22 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16373612 4141361 Cfmq3_m cystic fibrosis modifier QTL 3 (mouse) qtl MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20111116 MGI PMID:15921521 4141361 Cfmq3_m cystic fibrosis modifier QTL 3 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:15921521 4141361 Cfmq3_m cystic fibrosis modifier QTL 3 (mouse) qtl MP:0001858 intestinal inflammation IAGP N RGD:5509061 20111116 MGI PMID:15921521 4141361 Cfmq3_m cystic fibrosis modifier QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15921521 4141361 Cfmq3_m cystic fibrosis modifier QTL 3 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15921521 4141361 Cfmq3_m cystic fibrosis modifier QTL 3 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15921521 4141361 Cfmq3_m cystic fibrosis modifier QTL 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15921521 4141361 Cfmq3_m cystic fibrosis modifier QTL 3 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15921521 4141363 Nhdlq9_m non-HDL QTL 9 (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16685081 4141363 Nhdlq9_m non-HDL QTL 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16685081 4141365 Ltxs3_m lethal factor toxin susceptibility 3 (mouse) qtl MP:0002409 decreased susceptibility to infection IAGP N RGD:5509061 20111116 MGI PMID:14578173 4141365 Ltxs3_m lethal factor toxin susceptibility 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14578173 4141366 Mssq11_m mandible size and shape QTL 11 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141366 Mssq11_m mandible size and shape QTL 11 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141366 Mssq11_m mandible size and shape QTL 11 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4141369 Ccrs4_m corpus callosum hemisphere surface size 4 (mouse) qtl MP:0002196 absent corpus callosum IAGP N RGD:5509061 20111116 MGI PMID:16899052 4141369 Ccrs4_m corpus callosum hemisphere surface size 4 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16899052 4141370 Sox10m3_m Sox10Dom modifier 3 (mouse) qtl MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20111116 MGI PMID:15843399 4141370 Sox10m3_m Sox10Dom modifier 3 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15843399 4141371 Hydcs1_m hydrocephalus susceptibility 1 (mouse) qtl MP:0001891 hydrocephaly IAGP N RGD:5509061 20111116 MGI PMID:18509705 4141371 Hydcs1_m hydrocephalus susceptibility 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18509705 4141371 Hydcs1_m hydrocephalus susceptibility 1 (mouse) qtl MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20140221 MGI PMID:18509705 4141372 Bwtq12_m body weight QTL 12 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141372 Bwtq12_m body weight QTL 12 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141374 Bglu7_m blood glucose level 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4141374 Bglu7_m blood glucose level 7 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4141376 Dbm1_m diabetes modifier 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16964447 4141376 Dbm1_m diabetes modifier 1 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:16964447 4141376 Dbm1_m diabetes modifier 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16964447 4141376 Dbm1_m diabetes modifier 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16964447 4141376 Dbm1_m diabetes modifier 1 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:16964447 4141379 Rvil1_m radiation induced leukemia virus susceptibility (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6300845 4141379 Rvil1_m radiation induced leukemia virus susceptibility (mouse) qtl MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20111116 MGI PMID:6300845 4141383 Aia1_m autoimmune hemolytic anemia 1 (mouse) qtl MP:0004827 increased susceptibility to autoimmune hemolytic anemia IAGP N RGD:5509061 20111116 MGI PMID:7241566 4141383 Aia1_m autoimmune hemolytic anemia 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7241566 4141383 Aia1_m autoimmune hemolytic anemia 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7241566 4141385 Ccrs3_m corpus callosum hemisphere surface size 3 (mouse) qtl MP:0002196 absent corpus callosum IAGP N RGD:5509061 20111116 MGI PMID:16899052 4141385 Ccrs3_m corpus callosum hemisphere surface size 3 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16899052 4141386 Lctlp1_m lymph node cytotoxic T lymphocyte percentage 1 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17361202 4141386 Lctlp1_m lymph node cytotoxic T lymphocyte percentage 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17361202 4141386 Lctlp1_m lymph node cytotoxic T lymphocyte percentage 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17361202 4141386 Lctlp1_m lymph node cytotoxic T lymphocyte percentage 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17361202 4141386 Lctlp1_m lymph node cytotoxic T lymphocyte percentage 1 (mouse) qtl MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20111116 MGI PMID:17361202 4141387 Lgaq5_m late growth adjusted QTL 5 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141387 Lgaq5_m late growth adjusted QTL 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141389 Tailq7_m tail length QTL 7 (mouse) qtl MP:0000592 short tail IAGP N RGD:5509061 20111116 MGI PMID:17110492 4141389 Tailq7_m tail length QTL 7 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4141392 Albq6_m albuminuria QTL 6 (mouse) qtl MP:0002871 albuminuria IAGP N RGD:5509061 20111116 MGI PMID:17804484 4141392 Albq6_m albuminuria QTL 6 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17804484 4141392 Albq6_m albuminuria QTL 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17804484 4141393 Mol2_m modifier of LPS-response 2 (mouse) qtl MP:0001846 increased inflammatory response IAGP N RGD:5509061 20111116 MGI PMID:10585765 4141393 Mol2_m modifier of LPS-response 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10585765 4141394 Spw1_m spleen weight 1 (mouse) qtl MP:0004953 decreased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:18552208 4141394 Spw1_m spleen weight 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141394 Spw1_m spleen weight 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141395 Char2a_m P. chabaudi malaria resistance QTL 2a (mouse) qtl MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:16988259 4141395 Char2a_m P. chabaudi malaria resistance QTL 2a (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16988259 4141397 Adip16_m adiposity 16 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141397 Adip16_m adiposity 16 (mouse) qtl MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141397 Adip16_m adiposity 16 (mouse) qtl MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141398 Tgq22_m triglyceride QTL 22 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4141398 Tgq22_m triglyceride QTL 22 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4141399 Eac2_m ethyl alcohol consumption QTL 2 (mouse) qtl MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:17273929 4141399 Eac2_m ethyl alcohol consumption QTL 2 (mouse) qtl MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:17936574 4141399 Eac2_m ethyl alcohol consumption QTL 2 (mouse) qtl MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:17936574 4141399 Eac2_m ethyl alcohol consumption QTL 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17273929 4141400 Nilac8_m nicotine induced locomotor activity 8 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16176386 4141400 Nilac8_m nicotine induced locomotor activity 8 (mouse) qtl MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:16176386 4141401 Asdq3_m atrial septal defect QTL 3 (mouse) qtl MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20111116 MGI PMID:16484617 4141401 Asdq3_m atrial septal defect QTL 3 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16484617 4141402 T2dm1sa_m type 2 diabetes mellitus 1 in SMXA RI mice (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:12502510 4141402 T2dm1sa_m type 2 diabetes mellitus 1 in SMXA RI mice (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12502510 4141403 Salpa3_m serum alkaline phosphatase activity 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16159911 4141403 Salpa3_m serum alkaline phosphatase activity 3 (mouse) qtl MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20120209 MGI PMID:16159911 4141404 Mssq7_m mandible size and shape QTL 7 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141404 Mssq7_m mandible size and shape QTL 7 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141404 Mssq7_m mandible size and shape QTL 7 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4141405 Elda3_m ethanol induced low dose activation 3 (mouse) qtl MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20111116 MGI PMID:16792557 4141405 Elda3_m ethanol induced low dose activation 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16792557 4141409 Radsvq1_m radiation sensitivity QTL 1 (mouse) qtl MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20111116 MGI PMID:17378526 4141409 Radsvq1_m radiation sensitivity QTL 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17378526 4141410 Sfp4_m short free-running period 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19173005 4141410 Sfp4_m short free-running period 4 (mouse) qtl MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:19173005 4141412 Acsns1_m Angiostrongylus costaricensis nematode susceptibility 1 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:11862393 4141412 Acsns1_m Angiostrongylus costaricensis nematode susceptibility 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11862393 4141413 Mtgq2_m multiple trait growth QTL 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15457339 4141413 Mtgq2_m multiple trait growth QTL 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141413 Mtgq2_m multiple trait growth QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4141414 Brwt4_m brain weight 4 (mouse) qtl MP:0002176 increased brain weight IAGP N RGD:5509061 20111116 MGI PMID:1393606 4141414 Brwt4_m brain weight 4 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1393606 4141415 Tbt4_m trabecular bone traits 4 (mouse) qtl MP:0003795 abnormal bone structure IAGP N RGD:5509061 20111116 MGI PMID:16869725 4141415 Tbt4_m trabecular bone traits 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16869725 4141417 Esl1_m early lymphoma of SL 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8275476 4141417 Esl1_m early lymphoma of SL 1 (mouse) qtl MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8275476 4141418 Tmevp3_m Theiler's murine encephalomyelitis virus persistence 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10224268 4141418 Tmevp3_m Theiler's murine encephalomyelitis virus persistence 3 (mouse) qtl MP:0020938 decreased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:10224268 4141420 Catys1_m catalepsy susceptibility 1 (mouse) qtl MP:0002822 catalepsy IAGP N RGD:5509061 20111116 MGI PMID:14994542 4141420 Catys1_m catalepsy susceptibility 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14994542 4141422 Sh3_m sperm hammerhead 3 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17483418 4141422 Sh3_m sperm hammerhead 3 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17483418 4141422 Sh3_m sperm hammerhead 3 (mouse) qtl MP:0005578 teratozoospermia IAGP N RGD:5509061 20111116 MGI PMID:17483418 4141423 Nstr2_m nerve sheath tumor resistance QTL 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16397217 4141423 Nstr2_m nerve sheath tumor resistance QTL 2 (mouse) qtl MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:16397217 4141424 Drinknacl2_m drink sodium chloride 2 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20130503 MGI PMID:18363849 4141424 Drinknacl2_m drink sodium chloride 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141424 Drinknacl2_m drink sodium chloride 2 (mouse) qtl MP:0011941 increased fluid intake IAGP N RGD:5509061 20130503 MGI PMID:18363849 4141425 Anth_m resistance to Bacillus anthracis (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:2024449 4141425 Anth_m resistance to Bacillus anthracis (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:2024449 4141426 Wt3q3_m body weight, 3 weeks, QTL 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:10353911 4141426 Wt3q3_m body weight, 3 weeks, QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10353911 4141427 Grass1_m group A streptococcal sepsis severity 1 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:18421376 4141427 Grass1_m group A streptococcal sepsis severity 1 (mouse) qtl MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:18421376 4141427 Grass1_m group A streptococcal sepsis severity 1 (mouse) qtl MP:0005044 sepsis IAGP N RGD:5509061 20111116 MGI PMID:18421376 4141427 Grass1_m group A streptococcal sepsis severity 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18421376 4141427 Grass1_m group A streptococcal sepsis severity 1 (mouse) qtl MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20111116 MGI PMID:18421376 4141427 Grass1_m group A streptococcal sepsis severity 1 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18421376 4141429 Hdlq50_m HDL QTL 50 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16951076 4141429 Hdlq50_m HDL QTL 50 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16951076 4141430 Pbrbc2_m peripheral blood RBC 2 (mouse) qtl MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:17185011 4141430 Pbrbc2_m peripheral blood RBC 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17185011 4141431 Msmr2_m MSM lymphoma resistance 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8706013 4141431 Msmr2_m MSM lymphoma resistance 2 (mouse) qtl MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8706013 4141431 Msmr2_m MSM lymphoma resistance 2 (mouse) qtl MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8706013 4141431 Msmr2_m MSM lymphoma resistance 2 (mouse) qtl MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20131227 MGI PMID:8706013 4141432 Earheal2_m ear healing QTL 2 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:16208538 4141432 Earheal2_m ear healing QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16208538 4141433 Mleu3_m myeloid leukemia survival 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141433 Mleu3_m myeloid leukemia survival 3 (mouse) qtl MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20111116 MGI PMID:18552208 4141435 Fbtq3_m femoral bone trait QTL 3 (mouse) qtl MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20111116 MGI PMID:14584885 4141435 Fbtq3_m femoral bone trait QTL 3 (mouse) qtl MP:0003795 abnormal bone structure IAGP N RGD:5509061 20111116 MGI PMID:14584885 4141435 Fbtq3_m femoral bone trait QTL 3 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:14584885 4141435 Fbtq3_m femoral bone trait QTL 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14584885 4141436 Chldq7_m cholesterol and HDL QTL 7 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:17496333 4141436 Chldq7_m cholesterol and HDL QTL 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17496333 4141437 W10q14_m weight 10 weeks QTL 14 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141437 W10q14_m weight 10 weeks QTL 14 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141438 Skmw13_m skeletal muscle weight 13 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783642 4141438 Skmw13_m skeletal muscle weight 13 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16783642 4141438 Skmw13_m skeletal muscle weight 13 (mouse) qtl MP:0009423 increased extensor digitorum longus weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 4141439 Tgq5_m triglyceride QTL 5 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4141439 Tgq5_m triglyceride QTL 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4141440 Dmq1_m diet and mammary tumor QTL 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18288525 4141440 Dmq1_m diet and mammary tumor QTL 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18288525 4141440 Dmq1_m diet and mammary tumor QTL 1 (mouse) qtl MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:18288525 4141440 Dmq1_m diet and mammary tumor QTL 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18288525 4141444 spkw2_m spike wave 2 (mouse) qtl MP:0003216 absence seizures IAGP N RGD:5509061 20111116 MGI PMID:15800200 4141444 spkw2_m spike wave 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15800200 4141444 spkw2_m spike wave 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15800200 4141446 Ffaq4_m free fatty acid QTL 4 (mouse) qtl MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4141446 Ffaq4_m free fatty acid QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4141447 Cfmq2_m cystic fibrosis modifier QTL 2 (mouse) qtl MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20111116 MGI PMID:15921521 4141447 Cfmq2_m cystic fibrosis modifier QTL 2 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:15921521 4141447 Cfmq2_m cystic fibrosis modifier QTL 2 (mouse) qtl MP:0001858 intestinal inflammation IAGP N RGD:5509061 20111116 MGI PMID:15921521 4141447 Cfmq2_m cystic fibrosis modifier QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15921521 4141447 Cfmq2_m cystic fibrosis modifier QTL 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15921521 4141447 Cfmq2_m cystic fibrosis modifier QTL 2 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15921521 4141447 Cfmq2_m cystic fibrosis modifier QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15921521 4141447 Cfmq2_m cystic fibrosis modifier QTL 2 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15921521 4141448 Mpaps1_m microphthalmia anophthalmia susceptibility 1 (mouse) qtl MP:0001293 anophthalmia IAGP N RGD:5509061 20111116 MGI PMID:17196957 4141448 Mpaps1_m microphthalmia anophthalmia susceptibility 1 (mouse) qtl MP:0001297 microphthalmia IAGP N RGD:5509061 20111116 MGI PMID:17196957 4141448 Mpaps1_m microphthalmia anophthalmia susceptibility 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17196957 4141450 Bwtq11_m body weight QTL 11 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141450 Bwtq11_m body weight QTL 11 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141453 Mssq10_m mandible size and shape QTL 10 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141453 Mssq10_m mandible size and shape QTL 10 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141453 Mssq10_m mandible size and shape QTL 10 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4141455 Bwq8_m body weight QTL 8 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:17485926 4141455 Bwq8_m body weight QTL 8 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17485926 4141456 Vms2_m viral myocarditis susceptibility locus 2 (mouse) qtl MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20111116 MGI PMID:17287827 4141456 Vms2_m viral myocarditis susceptibility locus 2 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17287827 4141458 Sox10m4_m Sox10Dom modifier 4 (mouse) qtl MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20111116 MGI PMID:15843399 4141458 Sox10m4_m Sox10Dom modifier 4 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15843399 4141459 Plbcq4_m pleiotropic body composition QTL 4 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:18286334 4141459 Plbcq4_m pleiotropic body composition QTL 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18286334 4141460 Vmmt16_m vertebral morphology and mechanical traits 16 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4141460 Vmmt16_m vertebral morphology and mechanical traits 16 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4141462 Drinkmgcl23_m drink magnesium chloride 2 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141462 Drinkmgcl23_m drink magnesium chloride 2 3 (mouse) qtl MP:0011941 increased fluid intake IAGP N RGD:5509061 20130503 MGI PMID:18363849 4141463 Lynf3_m lymphocyte infiltration 3 (mouse) qtl MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20111116 MGI PMID:17703301 4141463 Lynf3_m lymphocyte infiltration 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17703301 4141464 Idd6.1_m insulin dependent diabetes susceptibility 6.1 (mouse) qtl MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20111116 MGI PMID:16893914 4141464 Idd6.1_m insulin dependent diabetes susceptibility 6.1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16893914 4141465 Dbm2_m diabetes modifier 2 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:16964447 4141465 Dbm2_m diabetes modifier 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16964447 4141465 Dbm2_m diabetes modifier 2 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:16964447 4141468 Nhdlq10_m non-HDL QTL 10 (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16685081 4141468 Nhdlq10_m non-HDL QTL 10 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16685081 4141469 Pldmq4_m pleiotropic diet and mammary tumor QTL 4 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18288525 4141469 Pldmq4_m pleiotropic diet and mammary tumor QTL 4 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18288525 4141469 Pldmq4_m pleiotropic diet and mammary tumor QTL 4 (mouse) qtl MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:18288525 4141469 Pldmq4_m pleiotropic diet and mammary tumor QTL 4 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18288525 4141470 Egq4_m early growth QTL 4 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141470 Egq4_m early growth QTL 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141472 Vmmt6_m vertebral morphology and mechanical traits 6 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4141472 Vmmt6_m vertebral morphology and mechanical traits 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4141476 Aem1_m antierythrocyte autoantibody modifier 1 (mouse) qtl MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:6618533 4141476 Aem1_m antierythrocyte autoantibody modifier 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6618533 4141477 Hemq5_m hematocrit QTL 5 (mouse) qtl MP:0002608 increased hematocrit IAGP N RGD:5509061 20111116 MGI PMID:16783647 4141477 Hemq5_m hematocrit QTL 5 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783647 4141478 Hbnr7_m Heligmosomoides bakeri nematode resistance 7 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14507332 4141478 Hbnr7_m Heligmosomoides bakeri nematode resistance 7 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:14507332 4141479 W10q8_m weight 10 weeks QTL 8 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141479 W10q8_m weight 10 weeks QTL 8 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141485 Abshq3_m abnormal sperm head QTL 3 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18689897 4141485 Abshq3_m abnormal sperm head QTL 3 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18689897 4141485 Abshq3_m abnormal sperm head QTL 3 (mouse) qtl MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20111116 MGI PMID:18689897 4141486 Idd5.4_m insulin dependent diabetes susceptibility 5.4 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:18056379 4141486 Idd5.4_m insulin dependent diabetes susceptibility 5.4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18056379 4141487 Tgq21_m triglyceride QTL 21 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4141487 Tgq21_m triglyceride QTL 21 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4141489 Spmd4_m spermatogenesis defect 4 (mouse) qtl MP:0002687 oligozoospermia IAGP N RGD:5509061 20111116 MGI PMID:16651692 4141489 Spmd4_m spermatogenesis defect 4 (mouse) qtl MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20111116 MGI PMID:16651692 4141489 Spmd4_m spermatogenesis defect 4 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16651692 4141489 Spmd4_m spermatogenesis defect 4 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16651692 4141490 Char2b_m P. chabaudi malaria resistance QTL 2b (mouse) qtl MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:16988259 4141490 Char2b_m P. chabaudi malaria resistance QTL 2b (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16988259 4141492 Adip17_m adiposity 17 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141492 Adip17_m adiposity 17 (mouse) qtl MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141492 Adip17_m adiposity 17 (mouse) qtl MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141492 Adip17_m adiposity 17 (mouse) qtl MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141493 Mmom4_m mammary modifier of Min 4 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18056448 4141493 Mmom4_m mammary modifier of Min 4 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18056448 4141493 Mmom4_m mammary modifier of Min 4 (mouse) qtl MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:18056448 4141493 Mmom4_m mammary modifier of Min 4 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18056448 4141494 Mohg6_m modifier of hg 6 (mouse) qtl MP:0000592 short tail IAGP N RGD:5509061 20111116 MGI PMID:16670015 4141494 Mohg6_m modifier of hg 6 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16670015 4141494 Mohg6_m modifier of hg 6 (mouse) qtl MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20111116 MGI PMID:16670015 4141494 Mohg6_m modifier of hg 6 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16670015 4141494 Mohg6_m modifier of hg 6 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16670015 4141494 Mohg6_m modifier of hg 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16670015 4141494 Mohg6_m modifier of hg 6 (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:16670015 4141495 Sh4_m sperm hammerhead 4 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17483418 4141495 Sh4_m sperm hammerhead 4 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17483418 4141495 Sh4_m sperm hammerhead 4 (mouse) qtl MP:0005578 teratozoospermia IAGP N RGD:5509061 20111116 MGI PMID:17483418 4141496 Krcn1_m keratoconus 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11773012 4141499 Wg2c_m weight gain in high growth mice 2c (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17694346 4141499 Wg2c_m weight gain in high growth mice 2c (mouse) qtl MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:17694346 4141499 Wg2c_m weight gain in high growth mice 2c (mouse) qtl MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:17694346 4141499 Wg2c_m weight gain in high growth mice 2c (mouse) qtl MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:17694346 4141502 Drinknh4cl1_m drink ammonium chloride 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141502 Drinknh4cl1_m drink ammonium chloride 1 (mouse) qtl MP:0011941 increased fluid intake IAGP N RGD:5509061 20130503 MGI PMID:18363849 4141504 Bodwt2_m body weight 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16387874 4141504 Bodwt2_m body weight 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16595606 4141504 Bodwt2_m body weight 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16595606 4141505 Chlq14_m circulating hormone level QTL 14 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:16782841 4141505 Chlq14_m circulating hormone level QTL 14 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16782841 4141506 Chlq7_m circulating hormone level QTL 7 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12865502 4141506 Chlq7_m circulating hormone level QTL 7 (mouse) qtl MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20111116 MGI PMID:12865502 4141508 Tailq8_m tail length QTL 8 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:17110492 4141508 Tailq8_m tail length QTL 8 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4141509 Pbrbc1_m peripheral blood RBC 1 (mouse) qtl MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:17185011 4141509 Pbrbc1_m peripheral blood RBC 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17185011 4141511 Gdcr1_m glycerolphosphate dehydrogenase regulator 1 (mouse) qtl MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20111116 MGI PMID:3996895 4141511 Gdcr1_m glycerolphosphate dehydrogenase regulator 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:3996895 4141512 Hdlq34_m HDL QTL 34 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16685081 4141512 Hdlq34_m HDL QTL 34 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16685081 4141513 Nhil3_m non-heme iron levels 3 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16799992 4141513 Nhil3_m non-heme iron levels 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16799992 4141513 Nhil3_m non-heme iron levels 3 (mouse) qtl MP:0008807 increased liver iron level IAGP N RGD:5509061 20111116 MGI PMID:16799992 4141514 Pbrbc3_m peripheral blood RBC 3 (mouse) qtl MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:17185011 4141514 Pbrbc3_m peripheral blood RBC 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17185011 4141515 Blmpf4_m bleomycin-induced pulmonary fibrosis 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:16179420 4141515 Blmpf4_m bleomycin-induced pulmonary fibrosis 4 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16179420 4141515 Blmpf4_m bleomycin-induced pulmonary fibrosis 4 (mouse) qtl MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20111116 MGI PMID:16179420 4141517 Gluchos1_m glucose homeostasis QTL 1 (mouse) qtl MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20111116 MGI PMID:16804088 4141517 Gluchos1_m glucose homeostasis QTL 1 (mouse) qtl MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20111116 MGI PMID:16804088 4141517 Gluchos1_m glucose homeostasis QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15729571 4141517 Gluchos1_m glucose homeostasis QTL 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15729571 4141518 Cia26_m collagen induced arthritis 26 (mouse) qtl MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20111116 MGI PMID:15611280 4141518 Cia26_m collagen induced arthritis 26 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15611280 4141518 Cia26_m collagen induced arthritis 26 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15611280 4141519 Hmtb5_m hemostasis and thrombosis bleeding time 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18787898 4141519 Hmtb5_m hemostasis and thrombosis bleeding time 5 (mouse) qtl MP:0005606 increased bleeding time IAGP N RGD:5509061 20111116 MGI PMID:18787898 4141520 Earheal3_m ear healing QTL 3 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:16208538 4141520 Earheal3_m ear healing QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16208538 4141521 Derms_m dermatitis susceptibility (mouse) qtl MP:0001194 dermatitis IAGP N RGD:5509061 20111116 MGI PMID:10570907 4141521 Derms_m dermatitis susceptibility (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10570907 4141521 Derms_m dermatitis susceptibility (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10570907 4141522 Rmp4_m resistance to mousepox 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7474114 4141522 Rmp4_m resistance to mousepox 4 (mouse) qtl MP:0020929 decreased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:7474114 4141523 Asdq2_m atrial septal defect QTL 2 (mouse) qtl MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20111116 MGI PMID:16484617 4141523 Asdq2_m atrial septal defect QTL 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16484617 4141524 Spw3_m spleen weight 3 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:18552208 4141524 Spw3_m spleen weight 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18552208 4141524 Spw3_m spleen weight 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141524 Spw3_m spleen weight 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141525 Gofm3_m gonadal fat mass 3 (mouse) qtl MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:16462940 4141525 Gofm3_m gonadal fat mass 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16462940 4141528 Azdm4_m Alzheimer's disease modifier 4 (mouse) qtl MP:0000604 amyloidosis IAGP N RGD:5509061 20111116 MGI PMID:16785251 4141528 Azdm4_m Alzheimer's disease modifier 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20140718 MGI Created by mouse qtl pipeline PMID:16785251 4141528 Azdm4_m Alzheimer's disease modifier 4 (mouse) qtl MP:0005395 obsolete other phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16785251 4141529 Mohg7_m modifier of hg 7 (mouse) qtl MP:0000592 short tail IAGP N RGD:5509061 20111116 MGI PMID:16670015 4141529 Mohg7_m modifier of hg 7 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16670015 4141529 Mohg7_m modifier of hg 7 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16670015 4141529 Mohg7_m modifier of hg 7 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16670015 4141529 Mohg7_m modifier of hg 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16670015 4141529 Mohg7_m modifier of hg 7 (mouse) qtl MP:0006086 decreased body mass index IAGP N RGD:5509061 20111116 MGI PMID:16670015 4141529 Mohg7_m modifier of hg 7 (mouse) qtl MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16670015 4141529 Mohg7_m modifier of hg 7 (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:16670015 4141532 Bmd1b_m bone mineral density 1b (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:16355278 4141532 Bmd1b_m bone mineral density 1b (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16355278 4141532 Bmd1b_m bone mineral density 1b (mouse) qtl MP:0003795 abnormal bone structure IAGP N RGD:5509061 20111116 MGI PMID:16355278 4141532 Bmd1b_m bone mineral density 1b (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16355278 4141532 Bmd1b_m bone mineral density 1b (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16355278 4141532 Bmd1b_m bone mineral density 1b (mouse) qtl MP:0013615 increased volumetric bone mineral density IAGP N RGD:5509061 20220922 MGI PMID:17416748 4141533 Mirb_m modifier of macrophage iron burden (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17632513 4141533 Mirb_m modifier of macrophage iron burden (mouse) qtl MP:0005638 hemochromatosis IAGP N RGD:5509061 20111116 MGI PMID:17632513 4141534 Dss1_m decreased sperm survival 1 (mouse) qtl MP:0002673 abnormal sperm number IAGP N RGD:5509061 20111116 MGI PMID:17483418 4141534 Dss1_m decreased sperm survival 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17483418 4141535 Bmnx_m body mass index (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17179051 4141535 Bmnx_m body mass index (mouse) qtl MP:0006087 increased body mass index IAGP N RGD:5509061 20111116 MGI PMID:17179051 4141536 Idd6.2_m insulin dependent diabetes susceptibility 6.2 (mouse) qtl MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20111116 MGI PMID:17353998 4141536 Idd6.2_m insulin dependent diabetes susceptibility 6.2 (mouse) qtl MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20111116 MGI PMID:16893914 4141536 Idd6.2_m insulin dependent diabetes susceptibility 6.2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16893914|PMID:17353998 4141536 Idd6.2_m insulin dependent diabetes susceptibility 6.2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16893914|PMID:17353998 4141536 Idd6.2_m insulin dependent diabetes susceptibility 6.2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16893914|PMID:17353998 4141536 Idd6.2_m insulin dependent diabetes susceptibility 6.2 (mouse) qtl MP:0008045 decreased NK cell number IAGP N RGD:5509061 20111116 MGI PMID:18641312 4141540 Rbcq2_m red blood cell QTL 2 (mouse) qtl MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:16596451 4141540 Rbcq2_m red blood cell QTL 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16596451 4141541 Tglq3_m triglyceride QTL 3 (mouse) qtl MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:17496333 4141541 Tglq3_m triglyceride QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17496333 4141543 Asq1_m autoimmune sialitis in IQI mice, associated locus 1 (mouse) qtl MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20111116 MGI PMID:17938903 4141543 Asq1_m autoimmune sialitis in IQI mice, associated locus 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17938903 4141543 Asq1_m autoimmune sialitis in IQI mice, associated locus 1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17938903 4141543 Asq1_m autoimmune sialitis in IQI mice, associated locus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17938903 4141544 Drinkmgcl22_m drink magnesium chloride 2 2 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4141544 Drinkmgcl22_m drink magnesium chloride 2 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141545 Tailaq2_m tail length adjusted QTL 2 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141545 Tailaq2_m tail length adjusted QTL 2 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141546 Mrdq3_m modifier of retinal degeneration QTL 3 (mouse) qtl MP:0001326 retina degeneration IAGP N RGD:5509061 20111116 MGI PMID:18344445 4141546 Mrdq3_m modifier of retinal degeneration QTL 3 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18344445 4141547 Dxcp1_m dexamethasone induced cleft palate 1 (mouse) qtl MP:0000111 cleft palate IAGP N RGD:5509061 20111116 MGI PMID:7157197 4141547 Dxcp1_m dexamethasone induced cleft palate 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:7157197 4141547 Dxcp1_m dexamethasone induced cleft palate 1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7157197 4141547 Dxcp1_m dexamethasone induced cleft palate 1 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7157197 4141548 Hdlq57_m HDL QTL 57 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18772481 4141548 Hdlq57_m HDL QTL 57 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18772481 4141549 W10q10_m weight 10 weeks QTL 10 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141549 W10q10_m weight 10 weeks QTL 10 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141550 Dbm3_m diabetes modifier 3 (mouse) qtl MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:16964447 4141550 Dbm3_m diabetes modifier 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16964447 4141552 Nhil5_m non-heme iron levels 5 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16799992 4141552 Nhil5_m non-heme iron levels 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16799992 4141552 Nhil5_m non-heme iron levels 5 (mouse) qtl MP:0008807 increased liver iron level IAGP N RGD:5509061 20111116 MGI PMID:16799992 4141553 Ath31_m atherosclerosis 31 (mouse) qtl MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20111116 MGI PMID:17641228 4141553 Ath31_m atherosclerosis 31 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17641228 4141554 Cfmq1_m cystic fibrosis modifier QTL 1 (mouse) qtl MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20111116 MGI PMID:15921521 4141554 Cfmq1_m cystic fibrosis modifier QTL 1 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:15921521 4141554 Cfmq1_m cystic fibrosis modifier QTL 1 (mouse) qtl MP:0001858 intestinal inflammation IAGP N RGD:5509061 20111116 MGI PMID:15921521 4141554 Cfmq1_m cystic fibrosis modifier QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15921521 4141554 Cfmq1_m cystic fibrosis modifier QTL 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15921521 4141554 Cfmq1_m cystic fibrosis modifier QTL 1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15921521 4141554 Cfmq1_m cystic fibrosis modifier QTL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15921521 4141554 Cfmq1_m cystic fibrosis modifier QTL 1 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15921521 4141555 Nbwa2_m NZB and NZW autoimmunity 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15034079 4141555 Nbwa2_m NZB and NZW autoimmunity 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15034079 4141555 Nbwa2_m NZB and NZW autoimmunity 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15034079 4141561 Blmpf5_m bleomycin-induced pulmonary fibrosis 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20141003 MGI Created by mouse qtl pipeline PMID:16179420 4141561 Blmpf5_m bleomycin-induced pulmonary fibrosis 5 (mouse) qtl MP:0005388 respiratory system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16179420 4141561 Blmpf5_m bleomycin-induced pulmonary fibrosis 5 (mouse) qtl MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20111116 MGI PMID:16179420 4141562 Pas3b_m pulmonary adenoma susceptibility 3b (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11584065 4141563 Lgq3_m late growth QTL 3 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141563 Lgq3_m late growth QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141564 Manr1_m multiple analgesic response 1 (mouse) qtl MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20111116 MGI PMID:18300945 4141564 Manr1_m multiple analgesic response 1 (mouse) qtl MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20111116 MGI PMID:18300945 4141564 Manr1_m multiple analgesic response 1 (mouse) qtl MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20111116 MGI PMID:18300945 4141564 Manr1_m multiple analgesic response 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18300945 4141564 Manr1_m multiple analgesic response 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18300945 4141565 Pbwg21_m postnatal body weight growth 21 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 4141565 Pbwg21_m postnatal body weight growth 21 (mouse) qtl MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20111116 MGI PMID:16174331 4141565 Pbwg21_m postnatal body weight growth 21 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16174331 4141567 Pldmq5_m pleiotropic diet and mammary tumor QTL 5 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18288525 4141567 Pldmq5_m pleiotropic diet and mammary tumor QTL 5 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18288525 4141567 Pldmq5_m pleiotropic diet and mammary tumor QTL 5 (mouse) qtl MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:18288525 4141567 Pldmq5_m pleiotropic diet and mammary tumor QTL 5 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18288525 4141568 Wght2_m weight 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16261418 4141568 Wght2_m weight 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261418 4141569 Vmmt17_m vertebral morphology and mechanical traits 17 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4141569 Vmmt17_m vertebral morphology and mechanical traits 17 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4141570 Lvwtq1_m liver weight QTL 1 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141570 Lvwtq1_m liver weight QTL 1 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4141575 Bwq10_m body weight QTL 10 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:18227763 4141575 Bwq10_m body weight QTL 10 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18227763 4141576 Mskt9_m musculoskeletal traits 9 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141576 Mskt9_m musculoskeletal traits 9 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141576 Mskt9_m musculoskeletal traits 9 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141577 Bmd38_m bone mineral density 38 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17308992 4141577 Bmd38_m bone mineral density 38 (mouse) qtl MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:17308992 4141580 Wbcc3_m white blood cell count 3 (mouse) qtl MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:18552208 4141580 Wbcc3_m white blood cell count 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141580 Wbcc3_m white blood cell count 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141582 Lgaq1_m late growth adjusted QTL 1 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141582 Lgaq1_m late growth adjusted QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141583 Drinknh4cl2_m drink ammonium chloride 2 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4141583 Drinknh4cl2_m drink ammonium chloride 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141587 Hdlq44_m HDL QTL 44 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16951076 4141587 Hdlq44_m HDL QTL 44 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16951076 4141587 Hdlq44_m HDL QTL 44 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18772481 4141587 Hdlq44_m HDL QTL 44 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18772481|PMID:16951076 4141587 Hdlq44_m HDL QTL 44 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:16951076 4141588 Qbis1_m QTL for body weight independent of sex 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16321990 4141588 Qbis1_m QTL for body weight independent of sex 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16321990 4141588 Qbis1_m QTL for body weight independent of sex 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16321990 4141588 Qbis1_m QTL for body weight independent of sex 1 (mouse) qtl MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16321990 4141591 Cq4_m cholesterol QTL 4 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:14974682 4141591 Cq4_m cholesterol QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14974682 4141592 Mtgq1_m multiple trait growth QTL 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15457339 4141592 Mtgq1_m multiple trait growth QTL 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141592 Mtgq1_m multiple trait growth QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 4141594 Fbtq4_m femoral bone trait QTL 4 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:14584885 4141594 Fbtq4_m femoral bone trait QTL 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14584885 4141595 Mpdk1_m modifier of polycystic kidney disease 1 (mouse) qtl MP:0002706 abnormal kidney size IAGP N RGD:5509061 20111116 MGI PMID:15728779 4141595 Mpdk1_m modifier of polycystic kidney disease 1 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15728779 4141595 Mpdk1_m modifier of polycystic kidney disease 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15728779 4141595 Mpdk1_m modifier of polycystic kidney disease 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15728779 4141597 Imacq_m isoflurane minimum alveolar concentration QTL (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17646494 4141597 Imacq_m isoflurane minimum alveolar concentration QTL (mouse) qtl MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20111116 MGI PMID:17646494 4141597 Imacq_m isoflurane minimum alveolar concentration QTL (mouse) qtl MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20111116 MGI PMID:17646494 4141598 Dbsq1_m diabetes susceptibility QTL 1 (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:16919419 4141598 Dbsq1_m diabetes susceptibility QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16919419 4141599 Exz2_m adrenal X zone degeneration 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:3582592 4141599 Exz2_m adrenal X zone degeneration 2 (mouse) qtl MP:0008303 early degeneration of the adrenal gland x-zone IAGP N RGD:5509061 20111116 MGI PMID:3582592 4141601 Pldmq3_m pleiotropic diet and mammary tumor QTL 3 (mouse) qtl MP:0001272 increased metastatic potential IAGP N RGD:5509061 20111116 MGI PMID:18288525 4141601 Pldmq3_m pleiotropic diet and mammary tumor QTL 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18288525 4141601 Pldmq3_m pleiotropic diet and mammary tumor QTL 3 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18288525 4141601 Pldmq3_m pleiotropic diet and mammary tumor QTL 3 (mouse) qtl MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:18288525 4141601 Pldmq3_m pleiotropic diet and mammary tumor QTL 3 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18288525 4141604 Idd4.3_m insulin dependent diabetes susceptibility 4.3 (mouse) qtl MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20140214 MGI PMID:16177100 4141604 Idd4.3_m insulin dependent diabetes susceptibility 4.3 (mouse) qtl MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20111116 MGI PMID:16177100 4141604 Idd4.3_m insulin dependent diabetes susceptibility 4.3 (mouse) qtl MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20111116 MGI PMID:16177100 4141604 Idd4.3_m insulin dependent diabetes susceptibility 4.3 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16177100 4141604 Idd4.3_m insulin dependent diabetes susceptibility 4.3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16177100 4141604 Idd4.3_m insulin dependent diabetes susceptibility 4.3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20220121 MGI Created by mouse qtl pipeline PMID:16177100|PMID:26512207 4141604 Idd4.3_m insulin dependent diabetes susceptibility 4.3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20140214 MGI Created by mouse qtl pipeline PMID:16177100 4141604 Idd4.3_m insulin dependent diabetes susceptibility 4.3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20220121 MGI Created by mouse qtl pipeline PMID:16177100|PMID:26512207 4141605 Plbcq5_m pleiotropic body composition QTL 5 (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:18286334 4141605 Plbcq5_m pleiotropic body composition QTL 5 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18286334 4141605 Plbcq5_m pleiotropic body composition QTL 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:18286334 4141605 Plbcq5_m pleiotropic body composition QTL 5 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:18286334 4141605 Plbcq5_m pleiotropic body composition QTL 5 (mouse) qtl MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:18286334 4141606 Bodwt1_m body weight 1 (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16387874 4141606 Bodwt1_m body weight 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16387874 4141606 Bodwt1_m body weight 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16595606 4141606 Bodwt1_m body weight 1 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:16387874 4141606 Bodwt1_m body weight 1 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16387874 4141606 Bodwt1_m body weight 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16595606 4141606 Bodwt1_m body weight 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16595606 4141607 Arp_m Arp lymphoid/erythroid hyperplasia (mouse) qtl MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20111116 MGI PMID:6973092 4141607 Arp_m Arp lymphoid/erythroid hyperplasia (mouse) qtl MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20111116 MGI PMID:6973092 4141607 Arp_m Arp lymphoid/erythroid hyperplasia (mouse) qtl MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20111116 MGI PMID:6973092 4141607 Arp_m Arp lymphoid/erythroid hyperplasia (mouse) qtl MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20111116 MGI PMID:6228526 4141607 Arp_m Arp lymphoid/erythroid hyperplasia (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:6973092|PMID:6228526 4141607 Arp_m Arp lymphoid/erythroid hyperplasia (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:6973092 4141607 Arp_m Arp lymphoid/erythroid hyperplasia (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20170421 MGI Created by mouse qtl pipeline PMID:6973092|PMID:6228526 4141607 Arp_m Arp lymphoid/erythroid hyperplasia (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6973092 4141607 Arp_m Arp lymphoid/erythroid hyperplasia (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20170421 MGI Created by mouse qtl pipeline PMID:6973092|PMID:6228526 4141607 Arp_m Arp lymphoid/erythroid hyperplasia (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6973092 4141607 Arp_m Arp lymphoid/erythroid hyperplasia (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20170421 MGI Created by mouse qtl pipeline PMID:6973092|PMID:6228526 4141607 Arp_m Arp lymphoid/erythroid hyperplasia (mouse) qtl MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20111116 MGI PMID:6973092 4141608 Phl1_m progressive hearing loss 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16897347 4141608 Phl1_m progressive hearing loss 1 (mouse) qtl MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20111116 MGI PMID:16897347 4141608 Phl1_m progressive hearing loss 1 (mouse) qtl MP:0004767 increased cochlear nerve compound action potential IAGP N RGD:5509061 20111116 MGI PMID:16897347 4141608 Phl1_m progressive hearing loss 1 (mouse) qtl MP:0005377 hearing/vestibular/ear phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16897347 4141609 Earheal4_m ear healing QTL 4 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:16208538 4141609 Earheal4_m ear healing QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16208538 4141610 Tailaq1_m tail length adjusted QTL 1 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141610 Tailaq1_m tail length adjusted QTL 1 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141611 Btts_m bitterness tasting (mouse) qtl MP:0004210 abnormal bitter taste sensitivity IAGP N RGD:5509061 20111116 MGI PMID:15938754 4141611 Btts_m bitterness tasting (mouse) qtl MP:0005394 taste/olfaction phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15938754 4141612 Cia40_m collagen induced arthritis 40 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:16507151 4141612 Cia40_m collagen induced arthritis 40 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16507151 4141612 Cia40_m collagen induced arthritis 40 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16507151 4141614 Lynf1_m lymphocyte infiltration 1 (mouse) qtl MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20111116 MGI PMID:17703301 4141614 Lynf1_m lymphocyte infiltration 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17703301 4141617 Ncilt_m nuclear cytoplasmic invaginations in lung tumors (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11293323 4141618 Brabq3_m brain amyloid beta QTL 3 (mouse) qtl MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20111116 MGI PMID:17400334 4141618 Brabq3_m brain amyloid beta QTL 3 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17400334 4141618 Brabq3_m brain amyloid beta QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20140718 MGI Created by mouse qtl pipeline PMID:17400334 4141618 Brabq3_m brain amyloid beta QTL 3 (mouse) qtl MP:0005395 obsolete other phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17400334 4141620 Bmrbc1_m bone marrow RBC 1 (mouse) qtl MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:17185011 4141620 Bmrbc1_m bone marrow RBC 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17185011 4141622 Dbacl_m diabetes accelerating locus (mouse) qtl MP:0004031 insulitis IAGP N RGD:5509061 20111116 MGI PMID:19167349 4141622 Dbacl_m diabetes accelerating locus (mouse) qtl MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20111116 MGI PMID:19167349 4141622 Dbacl_m diabetes accelerating locus (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19167349 4141622 Dbacl_m diabetes accelerating locus (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19167349 4141623 W6q13_m weight 6 weeks QTL 13 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141623 W6q13_m weight 6 weeks QTL 13 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141627 Bwq7_m body weight, QTL 7 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16547111 4141627 Bwq7_m body weight, QTL 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16547111 4141628 Tglq2_m triglyceride QTL 2 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:16254318 4141628 Tglq2_m triglyceride QTL 2 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:17496333 4141628 Tglq2_m triglyceride QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16254318|PMID:17496333 4141628 Tglq2_m triglyceride QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:16254318 4141629 Psds1_m psoriasis-like skin disease severity 1 (mouse) qtl MP:0001193 psoriasis IAGP N RGD:5509061 20111116 MGI PMID:17709541 4141629 Psds1_m psoriasis-like skin disease severity 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17709541 4141630 Gct6_m granulosa cell tumorigenesis 6 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14678975 4141630 Gct6_m granulosa cell tumorigenesis 6 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:14678975 4141630 Gct6_m granulosa cell tumorigenesis 6 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:14678975 4141630 Gct6_m granulosa cell tumorigenesis 6 (mouse) qtl MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20131227 MGI PMID:14678975 4141632 Drinkmgcl21_m drink magnesium chloride 2 1 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4141632 Drinkmgcl21_m drink magnesium chloride 2 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141632 Drinkmgcl21_m drink magnesium chloride 2 1 (mouse) qtl MP:0011941 increased fluid intake IAGP N RGD:5509061 20130503 MGI PMID:18363849 4141633 Idd6.3_m insulin dependent diabetes susceptibility 6.3 (mouse) qtl MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20111116 MGI PMID:16893914 4141633 Idd6.3_m insulin dependent diabetes susceptibility 6.3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16893914 4141636 Mohg8_m modifier of hg 8 (mouse) qtl MP:0000592 short tail IAGP N RGD:5509061 20111116 MGI PMID:16670015 4141636 Mohg8_m modifier of hg 8 (mouse) qtl MP:0001258 decreased body length IAGP N RGD:5509061 20111116 MGI PMID:16670015 4141636 Mohg8_m modifier of hg 8 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16670015 4141636 Mohg8_m modifier of hg 8 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16670015 4141636 Mohg8_m modifier of hg 8 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16670015 4141638 Pldmq2_m pleiotropic diet and mammary tumor QTL 2 (mouse) qtl MP:0001272 increased metastatic potential IAGP N RGD:5509061 20111116 MGI PMID:18288525 4141638 Pldmq2_m pleiotropic diet and mammary tumor QTL 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18288525 4141639 Wbcq6_m white blood cell quantitative locus 6 (mouse) qtl MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:16261417 4141639 Wbcq6_m white blood cell quantitative locus 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4141639 Wbcq6_m white blood cell quantitative locus 6 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4141640 Cxv1_m control of xenotropic virus 1 (mouse) qtl MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20111116 MGI PMID:6300850 4141640 Cxv1_m control of xenotropic virus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6300850 4141641 Fina1_m fat induced adiposity 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15870393 4141641 Fina1_m fat induced adiposity 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15870393 4141641 Fina1_m fat induced adiposity 1 (mouse) qtl MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20111116 MGI PMID:15870393 4141641 Fina1_m fat induced adiposity 1 (mouse) qtl MP:0010024 increased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:15870393 4141642 Ltxs2_m lethal factor toxin susceptibility 2 (mouse) qtl MP:0002409 decreased susceptibility to infection IAGP N RGD:5509061 20111116 MGI PMID:14578173 4141642 Ltxs2_m lethal factor toxin susceptibility 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14578173 4141643 Abshq6_m abnormal sperm head QTL 6 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18689897 4141643 Abshq6_m abnormal sperm head QTL 6 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18689897 4141643 Abshq6_m abnormal sperm head QTL 6 (mouse) qtl MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20111116 MGI PMID:18689897 4141646 Fecq3_m fecundity QTL 3 (mouse) qtl MP:0001934 increased litter size IAGP N RGD:5509061 20111116 MGI PMID:16547111 4141646 Fecq3_m fecundity QTL 3 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16547111 4141647 Hrvhf1_m heart rate variability, high frequency 1 (mouse) qtl MP:0003928 increased heart rate variability IAGP N RGD:5509061 20111116 MGI PMID:18456734 4141647 Hrvhf1_m heart rate variability, high frequency 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18456734 4141648 Tmc1m1_m Tmc1 modifier 1 (mouse) qtl MP:0001967 deafness IAGP N RGD:5509061 20111116 MGI PMID:16648588 4141648 Tmc1m1_m Tmc1 modifier 1 (mouse) qtl MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20111116 MGI PMID:16648588 4141648 Tmc1m1_m Tmc1 modifier 1 (mouse) qtl MP:0005377 hearing/vestibular/ear phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16648588 4141650 Chldq9_m cholesterol and HDL QTL 9 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:17496333 4141650 Chldq9_m cholesterol and HDL QTL 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17496333 4141651 Bglu6_m blood glucose level 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4141651 Bglu6_m blood glucose level 6 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4141652 Mrdq2_m modifier of retinal degeneration QTL 2 (mouse) qtl MP:0001326 retina degeneration IAGP N RGD:5509061 20111116 MGI PMID:18344445 4141652 Mrdq2_m modifier of retinal degeneration QTL 2 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18344445 4141654 Obq20_m obesity QTL 20 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141654 Obq20_m obesity QTL 20 (mouse) qtl MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141654 Obq20_m obesity QTL 20 (mouse) qtl MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141655 Mssq9_m mandible size and shape QTL 9 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141655 Mssq9_m mandible size and shape QTL 9 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141655 Mssq9_m mandible size and shape QTL 9 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4141657 Mohg1_m modifier of hg 1 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15965258 4141657 Mohg1_m modifier of hg 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15965258 4141657 Mohg1_m modifier of hg 1 (mouse) qtl MP:0006086 decreased body mass index IAGP N RGD:5509061 20111116 MGI PMID:16670015 4141659 Pbwg20_m postnatal body weight growth 20 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 4141659 Pbwg20_m postnatal body weight growth 20 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16174331 4141660 Nbwa1_m NZB and NZW autoimmunity 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15034079 4141662 Bglu4_m blood glucose level 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4141662 Bglu4_m blood glucose level 4 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4141666 Mleu5_m myeloid leukemia survival 5 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141666 Mleu5_m myeloid leukemia survival 5 (mouse) qtl MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20111116 MGI PMID:18552208 4141667 Dbm4_m diabetes modifier 4 (mouse) qtl MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:16964447 4141667 Dbm4_m diabetes modifier 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16964447 4141668 Pstc6_m periosteal circumference 6 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:17308992 4141668 Pstc6_m periosteal circumference 6 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17308992 4141668 Pstc6_m periosteal circumference 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17308992 4141669 Vmmt18_m vertebral morphology and mechanical traits 18 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4141669 Vmmt18_m vertebral morphology and mechanical traits 18 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4141673 Brml3_m bone response to mechanical loading 3 (mouse) qtl MP:0003795 abnormal bone structure IAGP N RGD:5509061 20111116 MGI PMID:16713414 4141673 Brml3_m bone response to mechanical loading 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16713414 4141674 Wght1_m weight 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16261418 4141674 Wght1_m weight 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261418 4141675 Lar_m low antibody response (mouse) qtl MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20111116 MGI PMID:1834548 4141675 Lar_m low antibody response (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1834548 4141676 Neogq1_m neonatal growth QTL 1 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:16547111 4141676 Neogq1_m neonatal growth QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16547111 4141678 Wbcc2_m white blood cell count 2 (mouse) qtl MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:18552208 4141678 Wbcc2_m white blood cell count 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141678 Wbcc2_m white blood cell count 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141681 Cia38_m collagen induced arthritis 38 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17312155 4141681 Cia38_m collagen induced arthritis 38 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:17312155 4141681 Cia38_m collagen induced arthritis 38 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17312155 4141681 Cia38_m collagen induced arthritis 38 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17312155 4141683 Rbcq1_m red blood cell QTL 1 (mouse) qtl MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:16596451 4141683 Rbcq1_m red blood cell QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16596451 4141685 Fbtq5_m femoral bone trait QTL 5 (mouse) qtl MP:0004149 increased bone strength IAGP N RGD:5509061 20111116 MGI PMID:14584885 4141685 Fbtq5_m femoral bone trait QTL 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14584885 4141685 Fbtq5_m femoral bone trait QTL 5 (mouse) qtl MP:0013615 increased volumetric bone mineral density IAGP N RGD:5509061 20220922 MGI PMID:14584885 4141686 Vms1_m viral myocarditis susceptibility locus 1 (mouse) qtl MP:0001856 myocarditis IAGP N RGD:5509061 20111116 MGI PMID:17287827 4141686 Vms1_m viral myocarditis susceptibility locus 1 (mouse) qtl MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20111116 MGI PMID:17287827 4141686 Vms1_m viral myocarditis susceptibility locus 1 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17287827 4141686 Vms1_m viral myocarditis susceptibility locus 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17287827 4141686 Vms1_m viral myocarditis susceptibility locus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17287827 4141687 Gofm1_m gonadal fat mass 1 (mouse) qtl MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:16462940 4141687 Gofm1_m gonadal fat mass 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16462940 4141690 Era1_m early running activity 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17969459 4141690 Era1_m early running activity 1 (mouse) qtl MP:0020474 advanced circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:17969459 4141691 Pbat2_m platelet-binding antibody-associated thrombocytopenia 2 (mouse) qtl MP:0003179 thrombocytopenia IAGP N RGD:5509061 20111116 MGI PMID:9754557 4141691 Pbat2_m platelet-binding antibody-associated thrombocytopenia 2 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:9754557 4141691 Pbat2_m platelet-binding antibody-associated thrombocytopenia 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9754557 4141691 Pbat2_m platelet-binding antibody-associated thrombocytopenia 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9754557 4141693 Adip15_m adiposity 15 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141693 Adip15_m adiposity 15 (mouse) qtl MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141696 Mssq19_m mandible size and shape QTL 19 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141696 Mssq19_m mandible size and shape QTL 19 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141696 Mssq19_m mandible size and shape QTL 19 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4141697 Hbnr3_m Heligmosomoides bakeri nematode resistance 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12647241 4141699 Ibdq2_m inflammatory bowel disease QTL 2 (mouse) qtl MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20111116 MGI PMID:15685547 4141699 Ibdq2_m inflammatory bowel disease QTL 2 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15685547 4141699 Ibdq2_m inflammatory bowel disease QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15685547 4141700 Ltsw1_m low testis weight 1 (mouse) qtl MP:0004852 decreased testis weight IAGP N RGD:5509061 20111116 MGI PMID:17483418 4141700 Ltsw1_m low testis weight 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17483418 4141700 Ltsw1_m low testis weight 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17483418 4141701 Tcnq3_m Tgfb1 trangenic F2 between C3H and NOD QTL 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:18160996 4141701 Tcnq3_m Tgfb1 trangenic F2 between C3H and NOD QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18160996 4141702 Hmtb6_m hemostasis and thrombosis rebleeding time 6 (mouse) qtl MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20111116 MGI PMID:18787898 4141702 Hmtb6_m hemostasis and thrombosis rebleeding time 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18787898 4141703 Chlq13_m circulating hormone level QTL 13 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:16782841 4141703 Chlq13_m circulating hormone level QTL 13 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16782841 4141704 Hipq1_m hyperinsulin production QTL 1 (mouse) qtl MP:0003058 increased insulin secretion IAGP N RGD:5509061 20111116 MGI PMID:17922105 4141704 Hipq1_m hyperinsulin production QTL 1 (mouse) qtl MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20111116 MGI PMID:17922105 4141704 Hipq1_m hyperinsulin production QTL 1 (mouse) qtl MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20111116 MGI PMID:17922105 4141704 Hipq1_m hyperinsulin production QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17922105 4141704 Hipq1_m hyperinsulin production QTL 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17922105 4141705 Mtgq4_m multiple trait growth QTL 4 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141705 Mtgq4_m multiple trait growth QTL 4 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:15457339 4141705 Mtgq4_m multiple trait growth QTL 4 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141705 Mtgq4_m multiple trait growth QTL 4 (mouse) qtl MP:0003397 increased muscle weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141705 Mtgq4_m multiple trait growth QTL 4 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141705 Mtgq4_m multiple trait growth QTL 4 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141705 Mtgq4_m multiple trait growth QTL 4 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 4141705 Mtgq4_m multiple trait growth QTL 4 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 4141705 Mtgq4_m multiple trait growth QTL 4 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 4141705 Mtgq4_m multiple trait growth QTL 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 4141705 Mtgq4_m multiple trait growth QTL 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 4141705 Mtgq4_m multiple trait growth QTL 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 4141705 Mtgq4_m multiple trait growth QTL 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 4141705 Mtgq4_m multiple trait growth QTL 4 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141705 Mtgq4_m multiple trait growth QTL 4 (mouse) qtl MP:0010024 increased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141708 Pbwg1.2_m postnatal body weight growth 1.2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17514348 4141708 Pbwg1.2_m postnatal body weight growth 1.2 (mouse) qtl MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20111116 MGI PMID:17514348 4141709 Plbcq3_m pleiotropic body composition QTL 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:18286334 4141709 Plbcq3_m pleiotropic body composition QTL 3 (mouse) qtl MP:0003960 increased lean body mass IAGP N RGD:5509061 20111116 MGI PMID:18286334 4141709 Plbcq3_m pleiotropic body composition QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18286334 4141710 Plast1a_m plasma plant sterol 1a (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16840795 4141710 Plast1a_m plasma plant sterol 1a (mouse) qtl MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20111116 MGI PMID:16840795 4141710 Plast1a_m plasma plant sterol 1a (mouse) qtl MP:0003192 increased cholesterol efflux IAGP N RGD:5509061 20111116 MGI PMID:16840795 4141710 Plast1a_m plasma plant sterol 1a (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16840795 4141710 Plast1a_m plasma plant sterol 1a (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16840795 4141710 Plast1a_m plasma plant sterol 1a (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16840795 4141711 Mohg9_m modifier of hg 9 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16670015 4141711 Mohg9_m modifier of hg 9 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:16670015 4141711 Mohg9_m modifier of hg 9 (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:16670015 4141712 Obwq1_m obesity and body weight QTL 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141712 Obwq1_m obesity and body weight QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141712 Obwq1_m obesity and body weight QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141712 Obwq1_m obesity and body weight QTL 1 (mouse) qtl MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141713 Pltq3_m platelet quantitative locus 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4141713 Pltq3_m platelet quantitative locus 3 (mouse) qtl MP:0005505 thrombocytosis IAGP N RGD:5509061 20111116 MGI PMID:16261417 4141714 Nhil1_m non-heme iron levels 1 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16799992 4141714 Nhil1_m non-heme iron levels 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16799992 4141714 Nhil1_m non-heme iron levels 1 (mouse) qtl MP:0008807 increased liver iron level IAGP N RGD:5509061 20111116 MGI PMID:16799992 4141716 Bmgr4_m bone marrow graft rejection 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17114464 4141716 Bmgr4_m bone marrow graft rejection 4 (mouse) qtl MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20111116 MGI PMID:17114464 4141717 Mskt2_m musculoskeletal traits 2 (mouse) qtl MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141717 Mskt2_m musculoskeletal traits 2 (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141717 Mskt2_m musculoskeletal traits 2 (mouse) qtl MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141717 Mskt2_m musculoskeletal traits 2 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141717 Mskt2_m musculoskeletal traits 2 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141717 Mskt2_m musculoskeletal traits 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141717 Mskt2_m musculoskeletal traits 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141717 Mskt2_m musculoskeletal traits 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141717 Mskt2_m musculoskeletal traits 2 (mouse) qtl MP:0009421 increased gastrocnemius weight IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141718 Imraq1_m immune response to AAV2 QTL 1 (mouse) qtl MP:0002493 increased IgG level IAGP N RGD:5509061 20111116 MGI PMID:15922957 4141718 Imraq1_m immune response to AAV2 QTL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15922957 4141718 Imraq1_m immune response to AAV2 QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15922957 4141720 Cath1_m carotid atherosclerosis 1 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:18048852 4141720 Cath1_m carotid atherosclerosis 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18048852 4141722 Mlca5_m modifier of locomotor activity 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16436185 4141722 Mlca5_m modifier of locomotor activity 5 (mouse) qtl MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:16436185 4141724 Idd5.1_m insulin dependent diabetes susceptibility 5.1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11016460|PMID:11723074 4141725 Wbcq4_m white blood cell quantitative locus 4 (mouse) qtl MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:16261417 4141725 Wbcq4_m white blood cell quantitative locus 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4141725 Wbcq4_m white blood cell quantitative locus 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4141726 Ssnt3_m short snout 3 (mouse) qtl MP:0000445 short snout IAGP N RGD:5509061 20111116 MGI PMID:14530301 4141726 Ssnt3_m short snout 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:14530301 4141726 Ssnt3_m short snout 3 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14530301 4141728 Egaq4_m early growth adjusted QTL 4 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141728 Egaq4_m early growth adjusted QTL 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141729 Drinkqhcl1_m drink quinine monohydrochloride 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141729 Drinkqhcl1_m drink quinine monohydrochloride 1 (mouse) qtl MP:0011941 increased fluid intake IAGP N RGD:5509061 20130503 MGI PMID:18363849 4141730 Nhdlq11_m non-HDL QTL 11 (mouse) qtl MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18048852 4141730 Nhdlq11_m non-HDL QTL 11 (mouse) qtl MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18048852 4141730 Nhdlq11_m non-HDL QTL 11 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18048852 4141730 Nhdlq11_m non-HDL QTL 11 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18048852 4141731 Mssq3_m mandible size and shape QTL 3 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141731 Mssq3_m mandible size and shape QTL 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141731 Mssq3_m mandible size and shape QTL 3 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4141733 Tmrdq1_m transmission ratio distortion QTL 1 (mouse) qtl MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20111116 MGI PMID:17506901 4141733 Tmrdq1_m transmission ratio distortion QTL 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17506901 4141734 Drinkcacl24_m drink calcium chloride 2 4 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4141734 Drinkcacl24_m drink calcium chloride 2 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141734 Drinkcacl24_m drink calcium chloride 2 4 (mouse) qtl MP:0011941 increased fluid intake IAGP N RGD:5509061 20130503 MGI PMID:18363849 4141738 Tgq23_m triglyceride QTL 23 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4141738 Tgq23_m triglyceride QTL 23 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4141740 Vmmt3_m vertebral morphology and mechanical traits 3 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4141740 Vmmt3_m vertebral morphology and mechanical traits 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4141744 Abshq7_m abnormal sperm head QTL 7 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18689897 4141744 Abshq7_m abnormal sperm head QTL 7 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18689897 4141744 Abshq7_m abnormal sperm head QTL 7 (mouse) qtl MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20111116 MGI PMID:18689897 4141745 Acla2_m anticardiolipin antibody 2 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:9754557 4141745 Acla2_m anticardiolipin antibody 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9754557 4141746 Vms3_m viral myocarditis susceptibility locus 3 (mouse) qtl MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20111116 MGI PMID:17287827 4141746 Vms3_m viral myocarditis susceptibility locus 3 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17287827 4141748 Mnek1c_m modifier of Nek1 (NIMA-related expressed kinase 1, kidney weight (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:10366444 4141748 Mnek1c_m modifier of Nek1 (NIMA-related expressed kinase 1, kidney weight (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10366444 4141748 Mnek1c_m modifier of Nek1 (NIMA-related expressed kinase 1, kidney weight (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:10366444 4141750 Modor3_m modifier of ocular retardation 3 (mouse) qtl MP:0002697 abnormal eye size IAGP N RGD:5509061 20111116 MGI PMID:16783634 4141750 Modor3_m modifier of ocular retardation 3 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783634 4141751 Tglq1_m triglyceride QTL 1 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:16254318 4141751 Tglq1_m triglyceride QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16254318 4141753 Vmmt19_m vertebral morphology and mechanical traits 19 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4141753 Vmmt19_m vertebral morphology and mechanical traits 19 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4141754 Fecq4_m fecundity QTL 4 (mouse) qtl MP:0001934 increased litter size IAGP N RGD:5509061 20111116 MGI PMID:16547111 4141754 Fecq4_m fecundity QTL 4 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:16547111 4141754 Fecq4_m fecundity QTL 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16547111 4141754 Fecq4_m fecundity QTL 4 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16547111 4141757 Sicd1_m seizure-induced cell death 1 (mouse) qtl MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20111116 MGI PMID:17439488 4141757 Sicd1_m seizure-induced cell death 1 (mouse) qtl MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20111116 MGI PMID:15281082 4141757 Sicd1_m seizure-induced cell death 1 (mouse) qtl MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20111116 MGI PMID:17439488 4141757 Sicd1_m seizure-induced cell death 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15281082|PMID:17996456 4141757 Sicd1_m seizure-induced cell death 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20151009 MGI Created by mouse qtl pipeline PMID:15281082 4141757 Sicd1_m seizure-induced cell death 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15281082|PMID:17996456 4141757 Sicd1_m seizure-induced cell death 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20151009 MGI Created by mouse qtl pipeline PMID:15281082 4141759 Dbmc3_m diabetes mRNA cluster 3 (mouse) qtl MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20111116 MGI PMID:12930764 4141759 Dbmc3_m diabetes mRNA cluster 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12930764 4141764 Tbt1_m trabecular bone traits 1 (mouse) qtl MP:0003795 abnormal bone structure IAGP N RGD:5509061 20111116 MGI PMID:16869725 4141764 Tbt1_m trabecular bone traits 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16869725 4141765 Mssq14_m mandible size and shape QTL 14 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141765 Mssq14_m mandible size and shape QTL 14 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141765 Mssq14_m mandible size and shape QTL 14 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4141767 Kwq15_m kidney weight QTL 15 (mouse) qtl MP:0003918 decreased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:17110492 4141767 Kwq15_m kidney weight QTL 15 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4141770 Tcpm1_m T-cell phenotype modifier 1 (mouse) qtl MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20111116 MGI PMID:8901605 4141770 Tcpm1_m T-cell phenotype modifier 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8901605 4141770 Tcpm1_m T-cell phenotype modifier 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8901605 4141771 Sbmd5_m spinal bone mineral density 5 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:17185055 4141771 Sbmd5_m spinal bone mineral density 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16183656 4141774 Mupm1_m major urinary protein modifier 1 (mouse) qtl MP:0001760 abnormal urine enzyme level IAGP N RGD:5509061 20111116 MGI PMID:2900461 4141774 Mupm1_m major urinary protein modifier 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:2900461 4141774 Mupm1_m major urinary protein modifier 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:2900461 4141775 Drinkcala1_m drink calcium lactate 1 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4141775 Drinkcala1_m drink calcium lactate 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141776 Nicoq3_m nicotine consumption QTL 3 (mouse) qtl MP:0002553 preference for addictive substance IAGP N RGD:5509061 20111116 MGI PMID:17010155 4141776 Nicoq3_m nicotine consumption QTL 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17010155 4141777 Abshq2_m abnormal sperm head QTL 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18689897 4141777 Abshq2_m abnormal sperm head QTL 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18689897 4141777 Abshq2_m abnormal sperm head QTL 2 (mouse) qtl MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20111116 MGI PMID:18689897 4141779 Ssrq8_m stress response QTL 8 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17913702 4141779 Ssrq8_m stress response QTL 8 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17913702 4141779 Ssrq8_m stress response QTL 8 (mouse) qtl MP:0010166 increased response to stress-induced hyperthermia IAGP N RGD:5509061 20111116 MGI PMID:17913702 4141781 Hdlq42_m HDL QTL 42 (mouse) qtl MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16951076 4141781 Hdlq42_m HDL QTL 42 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16951076 4141781 Hdlq42_m HDL QTL 42 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16951076 4141782 Mrdq5_m modifier of retinal degeneration QTL 5 (mouse) qtl MP:0001326 retina degeneration IAGP N RGD:5509061 20111116 MGI PMID:18344445 4141782 Mrdq5_m modifier of retinal degeneration QTL 5 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18344445 4141784 Vnhv1_m ventral hippocampal volume 1 (mouse) qtl MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20111116 MGI PMID:18721828 4141784 Vnhv1_m ventral hippocampal volume 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18721828 4141784 Vnhv1_m ventral hippocampal volume 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18721828 4141784 Vnhv1_m ventral hippocampal volume 1 (mouse) qtl MP:0008281 abnormal hippocampus size IAGP N RGD:5509061 20111116 MGI PMID:18721828 4141784 Vnhv1_m ventral hippocampal volume 1 (mouse) qtl MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20111116 MGI PMID:18721828 4141785 Eamcd1_m experimental autoimmune myocarditis 1 (mouse) qtl MP:0001856 myocarditis IAGP N RGD:5509061 20111116 MGI PMID:18951849 4141785 Eamcd1_m experimental autoimmune myocarditis 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18951849 4141785 Eamcd1_m experimental autoimmune myocarditis 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18951849 4141785 Eamcd1_m experimental autoimmune myocarditis 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18951849 4141785 Eamcd1_m experimental autoimmune myocarditis 1 (mouse) qtl MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20111116 MGI PMID:18951849 4141788 Suprmam1_m suppressor of mammary tumors 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17525270 4141788 Suprmam1_m suppressor of mammary tumors 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17525270 4141788 Suprmam1_m suppressor of mammary tumors 1 (mouse) qtl MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:17525270 4141788 Suprmam1_m suppressor of mammary tumors 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17525270 4141790 Hfem1_m Hfe modifier 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15131800 4141790 Hfem1_m Hfe modifier 1 (mouse) qtl MP:0005638 hemochromatosis IAGP N RGD:5509061 20111116 MGI PMID:15131800 4141791 W3q8_m weight 3 weeks QTL 8 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141791 W3q8_m weight 3 weeks QTL 8 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141792 Spmd1_m spermatogenesis defect 1 (mouse) qtl MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20111116 MGI PMID:16651692 4141792 Spmd1_m spermatogenesis defect 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16651692 4141792 Spmd1_m spermatogenesis defect 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20180302 MGI Created by mouse qtl pipeline PMID:16651692 4141792 Spmd1_m spermatogenesis defect 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16651692 4141792 Spmd1_m spermatogenesis defect 1 (mouse) qtl MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:16651692 4141794 Wbcq3_m white blood cell quantitative locus 3 (mouse) qtl MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:16261417 4141794 Wbcq3_m white blood cell quantitative locus 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4141794 Wbcq3_m white blood cell quantitative locus 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4141795 Tcnq4_m Tgfb1 trangenic F2 between C3H and NOD QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18160996 4141795 Tcnq4_m Tgfb1 trangenic F2 between C3H and NOD QTL 4 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:18160996 4141796 Drinkqhcl2_m drink quinine monohydrochloride 2 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4141796 Drinkqhcl2_m drink quinine monohydrochloride 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141797 Skmw16_m skeletal muscle weight 16 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783642 4141797 Skmw16_m skeletal muscle weight 16 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16783642 4141797 Skmw16_m skeletal muscle weight 16 (mouse) qtl MP:0009425 increased soleus weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 4141798 Egq6_m early growth QTL 6 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141798 Egq6_m early growth QTL 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141799 Albq9_m albuminuria QTL 9 (mouse) qtl MP:0002871 albuminuria IAGP N RGD:5509061 20111116 MGI PMID:17804484 4141799 Albq9_m albuminuria QTL 9 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17804484 4141799 Albq9_m albuminuria QTL 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17804484 4141801 Ath28_m atherosclerosis 28 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16373612 4141801 Ath28_m atherosclerosis 28 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16373612 4141802 Ignpq1_m IgA nephropathy QTL 1 (mouse) qtl MP:0002495 increased IgA level IAGP N RGD:5509061 20111116 MGI PMID:16316328 4141802 Ignpq1_m IgA nephropathy QTL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16316328 4141802 Ignpq1_m IgA nephropathy QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:16316328 4141803 Lmr30_m leishmaniasis resistance 30 (mouse) qtl MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:10508279 4141803 Lmr30_m leishmaniasis resistance 30 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10508279 4141804 Drinkcacl23_m drink calcium chloride 2 3 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4141804 Drinkcacl23_m drink calcium chloride 2 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141805 Sle19_m systematic lupus erythematosus susceptibility 19 (mouse) qtl MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:16943797 4141805 Sle19_m systematic lupus erythematosus susceptibility 19 (mouse) qtl MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20111116 MGI PMID:16943797 4141805 Sle19_m systematic lupus erythematosus susceptibility 19 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16943797 4141807 Asdq1_m atrial septal defect QTL 1 (mouse) qtl MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20111116 MGI PMID:16484617 4141807 Asdq1_m atrial septal defect QTL 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16484617 4141808 Mssq6_m mandible size and shape QTL 6 (mouse) qtl MP:0004592 small mandible IAGP N RGD:5509061 20111116 MGI PMID:19067046 4141808 Mssq6_m mandible size and shape QTL 6 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141808 Mssq6_m mandible size and shape QTL 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141808 Mssq6_m mandible size and shape QTL 6 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4141809 Pbwg1.1_m postnatal body weight growth 1.1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:17514348 4141809 Pbwg1.1_m postnatal body weight growth 1.1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17514348 4141811 Cia36_m collagen induced arthritis 36 (mouse) qtl MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17312155 4141811 Cia36_m collagen induced arthritis 36 (mouse) qtl MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:17312155 4141811 Cia36_m collagen induced arthritis 36 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17312155 4141811 Cia36_m collagen induced arthritis 36 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17312155 4141812 Mskt1_m musculoskeletal traits 1 (mouse) qtl MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141812 Mskt1_m musculoskeletal traits 1 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141812 Mskt1_m musculoskeletal traits 1 (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141812 Mskt1_m musculoskeletal traits 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141812 Mskt1_m musculoskeletal traits 1 (mouse) qtl MP:0004348 long femur IAGP N RGD:5509061 20181018 MGI PMID:15824847 4141812 Mskt1_m musculoskeletal traits 1 (mouse) qtl MP:0004357 long tibia IAGP N RGD:5509061 20181018 MGI PMID:15824847 4141812 Mskt1_m musculoskeletal traits 1 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141812 Mskt1_m musculoskeletal traits 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141812 Mskt1_m musculoskeletal traits 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141812 Mskt1_m musculoskeletal traits 1 (mouse) qtl MP:0006087 increased body mass index IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141813 Drinkkcl2_m drink potassium chloride 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141813 Drinkkcl2_m drink potassium chloride 2 (mouse) qtl MP:0011941 increased fluid intake IAGP N RGD:5509061 20130503 MGI PMID:18363849 4141815 Smtw2_m small testis weight 2 (mouse) qtl MP:0004852 decreased testis weight IAGP N RGD:5509061 20111116 MGI PMID:16651692 4141815 Smtw2_m small testis weight 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16651692 4141815 Smtw2_m small testis weight 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16651692 4141818 Brml1_m bone response to mechanical loading 1 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:16713414 4141818 Brml1_m bone response to mechanical loading 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16713414 4141818 Brml1_m bone response to mechanical loading 1 (mouse) qtl MP:0013615 increased volumetric bone mineral density IAGP N RGD:5509061 20220922 MGI PMID:16713414 4141819 Gofm2_m gonadal fat mass 2 (mouse) qtl MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:16462940 4141819 Gofm2_m gonadal fat mass 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16462940 4141821 Plbcq2_m pleiotropic body composition QTL 2 (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:18286334 4141821 Plbcq2_m pleiotropic body composition QTL 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18286334 4141821 Plbcq2_m pleiotropic body composition QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:18286334 4141821 Plbcq2_m pleiotropic body composition QTL 2 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:18286334 4141821 Plbcq2_m pleiotropic body composition QTL 2 (mouse) qtl MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:18286334 4141823 Mohg3_m modifier of hg 3 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15965258 4141823 Mohg3_m modifier of hg 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15965258 4141824 Ebmgr1_m epistatic bone marrow graft rejection 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17114464 4141824 Ebmgr1_m epistatic bone marrow graft rejection 1 (mouse) qtl MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20111116 MGI PMID:17114464 4141825 Hdlq37_m HDL QTL 37 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16685081 4141825 Hdlq37_m HDL QTL 37 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16685081 4141829 Lbm15_m lean body mass 15 (mouse) qtl MP:0003960 increased lean body mass IAGP N RGD:5509061 20111116 MGI PMID:17179051 4141829 Lbm15_m lean body mass 15 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17179051 4141830 Pregq1_m pregnancy QTL 1 (mouse) qtl MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20111116 MGI PMID:16547111 4141830 Pregq1_m pregnancy QTL 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16547111 4141832 Vmmt12_m vertebral morphology and mechanical traits 12 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4141832 Vmmt12_m vertebral morphology and mechanical traits 12 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4141833 W10q13_m weight 10 weeks QTL 13 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141833 W10q13_m weight 10 weeks QTL 13 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141834 Psrs4_m psoriasis susceptibility 4 (mouse) qtl MP:0001193 psoriasis IAGP N RGD:5509061 20111116 MGI PMID:16982899 4141834 Psrs4_m psoriasis susceptibility 4 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16982899 4141835 Fwth1_m facial width 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:14530301 4141835 Fwth1_m facial width 1 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14530301 4141835 Fwth1_m facial width 1 (mouse) qtl MP:0030069 broad face IAGP N RGD:5509061 20170921 MGI PMID:14530301 4141836 Tgq11_m triglyceride QTL 11 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4141836 Tgq11_m triglyceride QTL 11 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4141839 Chldq2_m cholesterol and HDL QTL 2 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16254318 4141839 Chldq2_m cholesterol and HDL QTL 2 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16254318 4141839 Chldq2_m cholesterol and HDL QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16254318 4141840 Pltq2_m platelet quantitative locus 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4141840 Pltq2_m platelet quantitative locus 2 (mouse) qtl MP:0005505 thrombocytosis IAGP N RGD:5509061 20111116 MGI PMID:16261417 4141843 Moen3_m modifier of engrailed QTL 3 (mouse) qtl MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20111116 MGI PMID:16884697 4141843 Moen3_m modifier of engrailed QTL 3 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16884697 4141844 Mssq15_m mandible size and shape QTL 15 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141844 Mssq15_m mandible size and shape QTL 15 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141844 Mssq15_m mandible size and shape QTL 15 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4141846 Eac5_m ethyl alcohol consumption QTL 4 (mouse) qtl MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:17273929 4141846 Eac5_m ethyl alcohol consumption QTL 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17273929 4141847 Obq21_m obesity QTL 21 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141847 Obq21_m obesity QTL 21 (mouse) qtl MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141848 Hdlq54_m HDL QTL 54 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18772481 4141848 Hdlq54_m HDL QTL 54 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18772481 4141849 Slms1_m sensitivity to locomotor stimulants 1 (mouse) qtl MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20111116 MGI PMID:17010097 4141849 Slms1_m sensitivity to locomotor stimulants 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17010097 4141850 Vnhv2_m ventral hippocampal volume 2 (mouse) qtl MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20111116 MGI PMID:18721828 4141850 Vnhv2_m ventral hippocampal volume 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18721828 4141850 Vnhv2_m ventral hippocampal volume 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18721828 4141850 Vnhv2_m ventral hippocampal volume 2 (mouse) qtl MP:0008281 abnormal hippocampus size IAGP N RGD:5509061 20111116 MGI PMID:18721828 4141850 Vnhv2_m ventral hippocampal volume 2 (mouse) qtl MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20111116 MGI PMID:18721828 4141851 Mtbcq7_m multiple trait body composition QTL 7 (mouse) qtl MP:0004232 decreased muscle weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141851 Mtbcq7_m multiple trait body composition QTL 7 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4141851 Mtbcq7_m multiple trait body composition QTL 7 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4141851 Mtbcq7_m multiple trait body composition QTL 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:17517159 4141851 Mtbcq7_m multiple trait body composition QTL 7 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141851 Mtbcq7_m multiple trait body composition QTL 7 (mouse) qtl MP:0010024 increased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141853 Skmw17_m skeletal muscle weight 17 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783642 4141853 Skmw17_m skeletal muscle weight 17 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16783642 4141853 Skmw17_m skeletal muscle weight 17 (mouse) qtl MP:0009423 increased extensor digitorum longus weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 4141854 T2dm2sa_m type 2 diabetes mellitus 2 in SMXA RI mice (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16447060 4141854 T2dm2sa_m type 2 diabetes mellitus 2 in SMXA RI mice (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:16447060 4141854 T2dm2sa_m type 2 diabetes mellitus 2 in SMXA RI mice (mouse) qtl MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20111116 MGI PMID:16447060 4141854 T2dm2sa_m type 2 diabetes mellitus 2 in SMXA RI mice (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16447060 4141854 T2dm2sa_m type 2 diabetes mellitus 2 in SMXA RI mice (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16447060 4141854 T2dm2sa_m type 2 diabetes mellitus 2 in SMXA RI mice (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16447060 4141854 T2dm2sa_m type 2 diabetes mellitus 2 in SMXA RI mice (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:16447060 4141854 T2dm2sa_m type 2 diabetes mellitus 2 in SMXA RI mice (mouse) qtl MP:0006087 increased body mass index IAGP N RGD:5509061 20111116 MGI PMID:16447060 4141854 T2dm2sa_m type 2 diabetes mellitus 2 in SMXA RI mice (mouse) qtl MP:0010024 increased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:16447060 4141855 Pbwg22_m postnatal body weight growth 22 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 4141855 Pbwg22_m postnatal body weight growth 22 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16174331 4141859 amd_m autoimmune myocardial disease (mouse) qtl MP:0001856 myocarditis IAGP N RGD:5509061 20111116 MGI PMID:1657464 4141859 amd_m autoimmune myocardial disease (mouse) qtl MP:0001856 myocarditis IAGP N RGD:5509061 20111116 MGI PMID:1848043 4141859 amd_m autoimmune myocardial disease (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1848043 4141859 amd_m autoimmune myocardial disease (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:1848043 4141861 Hdlq43_m HDL QTL 43 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16951076 4141861 Hdlq43_m HDL QTL 43 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16951076 4141862 Nilac9_m nicotine induced locomotor activity 9 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16176386 4141862 Nilac9_m nicotine induced locomotor activity 9 (mouse) qtl MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:16176386 4141862 Nilac9_m nicotine induced locomotor activity 9 (mouse) qtl MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:19083055 4141863 Ftms1_m fat mass 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16254318 4141863 Ftms1_m fat mass 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:16254318 4141863 Ftms1_m fat mass 1 (mouse) qtl MP:0010024 increased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:16254318 4141864 Mrdq4_m modifier of retinal degeneration QTL 4 (mouse) qtl MP:0001326 retina degeneration IAGP N RGD:5509061 20111116 MGI PMID:18344445 4141864 Mrdq4_m modifier of retinal degeneration QTL 4 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18344445 4141865 Spw2_m spleen weight 2 (mouse) qtl MP:0004953 decreased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:18552208 4141865 Spw2_m spleen weight 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141865 Spw2_m spleen weight 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4141866 Vmmt10_m vertebral morphology and mechanical traits 10 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4141866 Vmmt10_m vertebral morphology and mechanical traits 10 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4141867 Tcnq1_m Tgfb1 trangenic F2 between C3H and NOD QTL 1 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:18160996 4141867 Tcnq1_m Tgfb1 trangenic F2 between C3H and NOD QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18160996 4141868 Hmtb1_m hemostasis and thrombosis 1 (mouse) qtl MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20111116 MGI PMID:17022820 4141868 Hmtb1_m hemostasis and thrombosis 1 (mouse) qtl MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20111116 MGI PMID:17022820 4141868 Hmtb1_m hemostasis and thrombosis 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17022820 4141868 Hmtb1_m hemostasis and thrombosis 1 (mouse) qtl MP:0005607 decreased bleeding time IAGP N RGD:5509061 20111116 MGI PMID:17022820 4141869 W6q12_m weight 6 weeks QTL 12 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141869 W6q12_m weight 6 weeks QTL 12 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141870 Dbsq2_m diabetes susceptibility QTL 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16919419 4141870 Dbsq2_m diabetes susceptibility QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16919419 4141872 Psrs5_m psoriasis susceptibility 5 (mouse) qtl MP:0001193 psoriasis IAGP N RGD:5509061 20111116 MGI PMID:16982899 4141872 Psrs5_m psoriasis susceptibility 5 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16982899 4141874 Drinkmgcl25_m drink magnesium chloride 2 5 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4141874 Drinkmgcl25_m drink magnesium chloride 2 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141876 Lskpf3_m LSK cell population frequency 3 (mouse) qtl MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20111116 MGI PMID:18288524 4141876 Lskpf3_m LSK cell population frequency 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18288524 4141879 Chlq9_m circulating hormone level QTL 9 (mouse) qtl MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:16782841 4141879 Chlq9_m circulating hormone level QTL 9 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:16782841 4141879 Chlq9_m circulating hormone level QTL 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16782841 4141881 Mnic3_m macronutrient intake, carbohydrate 3 (mouse) qtl MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20111116 MGI PMID:12388789 4141881 Mnic3_m macronutrient intake, carbohydrate 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12388789 4141883 Mpdk2_m modifier of polycystic kidney disease 2 (mouse) qtl MP:0002706 abnormal kidney size IAGP N RGD:5509061 20111116 MGI PMID:15728779 4141883 Mpdk2_m modifier of polycystic kidney disease 2 (mouse) qtl MP:0003254 bile duct inflammation IAGP N RGD:5509061 20111116 MGI PMID:15728779 4141883 Mpdk2_m modifier of polycystic kidney disease 2 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15728779 4141883 Mpdk2_m modifier of polycystic kidney disease 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15728779 4141883 Mpdk2_m modifier of polycystic kidney disease 2 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15728779 4141883 Mpdk2_m modifier of polycystic kidney disease 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15728779 4141883 Mpdk2_m modifier of polycystic kidney disease 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15728779 4141885 Cspt_m CD8 single positive T cell (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15780994 4141885 Cspt_m CD8 single positive T cell (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15780994 4141885 Cspt_m CD8 single positive T cell (mouse) qtl MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20111116 MGI PMID:15780994 4141887 Drinkcacl22_m drink calcium chloride 2 2 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4141887 Drinkcacl22_m drink calcium chloride 2 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141888 Vgot2_m vaginal opening timing 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15284200 4141888 Vgot2_m vaginal opening timing 2 (mouse) qtl MP:0008994 early vaginal opening IAGP N RGD:5509061 20111116 MGI PMID:15284200 4141889 Qui_m quinine sensitivity, taste (mouse) qtl MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20111116 MGI PMID:10480673 4141889 Qui_m quinine sensitivity, taste (mouse) qtl MP:0002850 saccharin preference IAGP N RGD:5509061 20111116 MGI PMID:10480673 4141889 Qui_m quinine sensitivity, taste (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10480673 4141889 Qui_m quinine sensitivity, taste (mouse) qtl MP:0005394 taste/olfaction phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10480673 4141890 Hdlq48_m HDL QTL 48 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16951076 4141890 Hdlq48_m HDL QTL 48 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16951076 4141891 Bmgr2_m bone marrow graft rejection 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17114464 4141891 Bmgr2_m bone marrow graft rejection 2 (mouse) qtl MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20111116 MGI PMID:17114464 4141893 Mssq5_m mandible size and shape QTL 5 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141893 Mssq5_m mandible size and shape QTL 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141893 Mssq5_m mandible size and shape QTL 5 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4141894 Nidd6k_m Nidd6 on KK-A (mouse) qtl MP:0000189 hypoglycemia IAGP N RGD:5509061 20111116 MGI PMID:12115031 4141894 Nidd6k_m Nidd6 on KK-A (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115031 4141895 Dbmc1_m diabetes mRNA cluster 1 (mouse) qtl MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20111116 MGI PMID:12930764 4141895 Dbmc1_m diabetes mRNA cluster 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12930764 4141897 Imrfq2_m immune response to Factor IX QTL 2 (mouse) qtl MP:0002493 increased IgG level IAGP N RGD:5509061 20111116 MGI PMID:15922957 4141897 Imrfq2_m immune response to Factor IX QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15922957 4141897 Imrfq2_m immune response to Factor IX QTL 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15922957 4141898 Gfpq1_m gonadal fat pad weight QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4141898 Gfpq1_m gonadal fat pad weight QTL 1 (mouse) qtl MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:17110492 4141899 Pldmq1_m pleiotropic diet and mammary tumor QTL 1 (mouse) qtl MP:0001272 increased metastatic potential IAGP N RGD:5509061 20111116 MGI PMID:18288525 4141899 Pldmq1_m pleiotropic diet and mammary tumor QTL 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18288525 4141899 Pldmq1_m pleiotropic diet and mammary tumor QTL 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18288525 4141899 Pldmq1_m pleiotropic diet and mammary tumor QTL 1 (mouse) qtl MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:18288525 4141899 Pldmq1_m pleiotropic diet and mammary tumor QTL 1 (mouse) qtl MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:18288525 4141899 Pldmq1_m pleiotropic diet and mammary tumor QTL 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18288525 4141902 Cia37_m collagen induced arthritis 37 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17312155 4141902 Cia37_m collagen induced arthritis 37 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:17312155 4141902 Cia37_m collagen induced arthritis 37 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17312155 4141902 Cia37_m collagen induced arthritis 37 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17312155 4141904 Mpdk4_m modifier of polycystic kidney disease 4 (mouse) qtl MP:0002706 abnormal kidney size IAGP N RGD:5509061 20111116 MGI PMID:15728779 4141904 Mpdk4_m modifier of polycystic kidney disease 4 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15728779 4141904 Mpdk4_m modifier of polycystic kidney disease 4 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15728779 4141904 Mpdk4_m modifier of polycystic kidney disease 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15728779 4141906 Tgq4_m triglyceride QTL 4 (mouse) qtl MP:0005317 increased triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4141906 Tgq4_m triglyceride QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4141909 W10q18_m weight 10 weeks QTL 18 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141909 W10q18_m weight 10 weeks QTL 18 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141911 W6q15_m weight 6 weeks QTL 15 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141911 W6q15_m weight 6 weeks QTL 15 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141912 Fatpad3_m fat pad 3 (mouse) qtl MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:16545150 4141912 Fatpad3_m fat pad 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16545150 4141912 Fatpad3_m fat pad 3 (mouse) qtl MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16545150 4141913 Myci2_m myocardial infarction 2 (mouse) qtl MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20111116 MGI PMID:9754557 4141913 Myci2_m myocardial infarction 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9754557 4141913 Myci2_m myocardial infarction 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9754557 4141914 Gcsfis_m G-CSF induced splenomegaly (mouse) qtl MP:0000691 enlarged spleen IAGP N RGD:5509061 20111116 MGI PMID:10764151 4141914 Gcsfis_m G-CSF induced splenomegaly (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:10764151 4141914 Gcsfis_m G-CSF induced splenomegaly (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10764151 4141914 Gcsfis_m G-CSF induced splenomegaly (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10764151 4141915 Mskt4_m musculoskeletal traits 4 (mouse) qtl MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141915 Mskt4_m musculoskeletal traits 4 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141915 Mskt4_m musculoskeletal traits 4 (mouse) qtl MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141915 Mskt4_m musculoskeletal traits 4 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141915 Mskt4_m musculoskeletal traits 4 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141915 Mskt4_m musculoskeletal traits 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141915 Mskt4_m musculoskeletal traits 4 (mouse) qtl MP:0009421 increased gastrocnemius weight IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141916 Drinkcacl25_m drink calcium chloride 2 5 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4141916 Drinkcacl25_m drink calcium chloride 2 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141918 Diwg1_m diet-induced weight gain 1 (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:15561960 4141918 Diwg1_m diet-induced weight gain 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561960 4141918 Diwg1_m diet-induced weight gain 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561960 4141918 Diwg1_m diet-induced weight gain 1 (mouse) qtl MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20111116 MGI PMID:15561960 4141919 Fwth2_m facial width 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:14530301 4141919 Fwth2_m facial width 2 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14530301 4141919 Fwth2_m facial width 2 (mouse) qtl MP:0030069 broad face IAGP N RGD:5509061 20170921 MGI PMID:14530301 4141920 Vmmt5_m vertebral morphology and mechanical traits 5 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4141920 Vmmt5_m vertebral morphology and mechanical traits 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4141924 Brml2_m bone response to mechanical loading 2 (mouse) qtl MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20111116 MGI PMID:16713414 4141924 Brml2_m bone response to mechanical loading 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16713414 4141924 Brml2_m bone response to mechanical loading 2 (mouse) qtl MP:0013615 increased volumetric bone mineral density IAGP N RGD:5509061 20220922 MGI PMID:16713414 4141925 Iva2_m isovaleric acid smelling 2 (mouse) qtl MP:0001984 abnormal olfaction IAGP N RGD:5509061 20111116 MGI PMID:8521470 4141925 Iva2_m isovaleric acid smelling 2 (mouse) qtl MP:0005394 taste/olfaction phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8521470 4141926 Pscr3_m corneal resistance to P. aeruginosa 3 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:3674828 4141926 Pscr3_m corneal resistance to P. aeruginosa 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:3674828 4141929 Chlq18_m circulating hormone level QTL 18 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:16782841 4141929 Chlq18_m circulating hormone level QTL 18 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16782841 4141931 Vmmt13_m vertebral morphology and mechanical traits 13 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4141931 Vmmt13_m vertebral morphology and mechanical traits 13 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4141933 Mnif3_m macronutrient intake, fat 3 (mouse) qtl MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20111116 MGI PMID:12388789 4141933 Mnif3_m macronutrient intake, fat 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12388789 4141934 Mtbcq6_m multiple trait body composition QTL 6 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141934 Mtbcq6_m multiple trait body composition QTL 6 (mouse) qtl MP:0003402 decreased liver weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141934 Mtbcq6_m multiple trait body composition QTL 6 (mouse) qtl MP:0003918 decreased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141934 Mtbcq6_m multiple trait body composition QTL 6 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4141934 Mtbcq6_m multiple trait body composition QTL 6 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4141934 Mtbcq6_m multiple trait body composition QTL 6 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4141934 Mtbcq6_m multiple trait body composition QTL 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4141934 Mtbcq6_m multiple trait body composition QTL 6 (mouse) qtl MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141934 Mtbcq6_m multiple trait body composition QTL 6 (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141935 Tgq15_m triglyceride QTL 15 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4141935 Tgq15_m triglyceride QTL 15 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4141936 Mohg2_m modifier of hg 2 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15965258 4141936 Mohg2_m modifier of hg 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15965258 4141938 Mssq12_m mandible size and shape QTL 12 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141938 Mssq12_m mandible size and shape QTL 12 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4141938 Mssq12_m mandible size and shape QTL 12 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4141939 Pregq2_m pregnancy QTL 2 (mouse) qtl MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20111116 MGI PMID:16547111 4141939 Pregq2_m pregnancy QTL 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16547111 4141940 W6q5_m weight 6 weeks QTL 5 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141940 W6q5_m weight 6 weeks QTL 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141941 Bmd21_m bone mineral density 21 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:16355279 4141941 Bmd21_m bone mineral density 21 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16355279 4141942 Drinkmgcl24_m drink magnesium chloride 2 4 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20130503 MGI PMID:18363849 4141942 Drinkmgcl24_m drink magnesium chloride 2 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141943 W6q6_m weight 6 weeks QTL 6 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141943 W6q6_m weight 6 weeks QTL 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141944 Tbt3_m trabecular bone traits 3 (mouse) qtl MP:0003795 abnormal bone structure IAGP N RGD:5509061 20111116 MGI PMID:16869725 4141944 Tbt3_m trabecular bone traits 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16869725 4141945 Il4ppq_m IL-4 producing potential QTL (mouse) qtl MP:0002962 increased urine protein level IAGP N RGD:5509061 20111116 MGI PMID:17189592 4141945 Il4ppq_m IL-4 producing potential QTL (mouse) qtl MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20111116 MGI PMID:17189592 4141945 Il4ppq_m IL-4 producing potential QTL (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17189592 4141945 Il4ppq_m IL-4 producing potential QTL (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17189592 4141945 Il4ppq_m IL-4 producing potential QTL (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17189592 4141948 Eac4_m ethyl alcohol consumption QTL 4 (mouse) qtl MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:17273929 4141948 Eac4_m ethyl alcohol consumption QTL 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17273929 4141950 Hbnr8_m Heligmosomoides bakeri nematode resistance 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14507332 4141951 Chldq1_m cholesterol and HDL QTL 1 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16254318 4141951 Chldq1_m cholesterol and HDL QTL 1 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16254318 4141951 Chldq1_m cholesterol and HDL QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16254318 4141952 W3q7_m weight 3 weeks QTL 7 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141952 W3q7_m weight 3 weeks QTL 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141954 Obwq3_m obesity and body weight QTL 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141954 Obwq3_m obesity and body weight QTL 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141954 Obwq3_m obesity and body weight QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141954 Obwq3_m obesity and body weight QTL 3 (mouse) qtl MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141954 Obwq3_m obesity and body weight QTL 3 (mouse) qtl MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141955 Hemq4_m hematocrit QTL 4 (mouse) qtl MP:0002608 increased hematocrit IAGP N RGD:5509061 20111116 MGI PMID:16783647 4141955 Hemq4_m hematocrit QTL 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783647 4141956 Egq7_m early growth QTL 7 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141956 Egq7_m early growth QTL 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141958 Gofm4_m gonadal fat mass 4 (mouse) qtl MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:16462940 4141958 Gofm4_m gonadal fat mass 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16462940 4141959 Chlq8_m circulating hormone level QTL 8 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12865502 4141959 Chlq8_m circulating hormone level QTL 8 (mouse) qtl MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20111116 MGI PMID:12865502 4141960 Rosq1_m reactive oxygen species QTL 1 (mouse) qtl MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20111116 MGI PMID:17361202 4141960 Rosq1_m reactive oxygen species QTL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17361202 4141960 Rosq1_m reactive oxygen species QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:17361202 4141961 Tbrs4_m tuberculosis resistance 4 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:12740444 4141961 Tbrs4_m tuberculosis resistance 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12740444 4141962 Hypn2_m hyperinsulinemia 2 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:15561960 4141962 Hypn2_m hyperinsulinemia 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561960 4141963 Vactq1_m voluntary activity QTL 1 (mouse) qtl MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20111116 MGI PMID:18171721 4141963 Vactq1_m voluntary activity QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18171721 4141964 Obrq16_m obesity resistance QTL 16 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19137372 4141964 Obrq16_m obesity resistance QTL 16 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19137372 4141964 Obrq16_m obesity resistance QTL 16 (mouse) qtl MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:19137372 4141966 Tailq1_m tail length QTL 1 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141966 Tailq1_m tail length QTL 1 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141967 Fbrwt1_m forebrain weight 1 (mouse) qtl MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20111116 MGI PMID:18817551 4141967 Fbrwt1_m forebrain weight 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18817551 4141968 Tcnq2_m Tgfb1 trangenic F2 between C3H and NOD QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18160996 4141968 Tcnq2_m Tgfb1 trangenic F2 between C3H and NOD QTL 2 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:18160996 4141969 Egaq3_m early growth adjusted QTL 3 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141969 Egaq3_m early growth adjusted QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141970 Obq22_m obesity QTL 22 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141970 Obq22_m obesity QTL 22 (mouse) qtl MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141970 Obq22_m obesity QTL 22 (mouse) qtl MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141971 Plast2a_m plasma plant sterol 2a (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12446833 4141971 Plast2a_m plasma plant sterol 2a (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12446833 4141973 Adip18_m adiposity 18 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4141973 Adip18_m adiposity 18 (mouse) qtl MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141973 Adip18_m adiposity 18 (mouse) qtl MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4141974 Skmw14_m skeletal muscle weight 14 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783642 4141974 Skmw14_m skeletal muscle weight 14 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16783642 4141974 Skmw14_m skeletal muscle weight 14 (mouse) qtl MP:0009425 increased soleus weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 4141975 Sh1_m sperm hammerhead 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17483418 4141975 Sh1_m sperm hammerhead 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17483418 4141975 Sh1_m sperm hammerhead 1 (mouse) qtl MP:0005578 teratozoospermia IAGP N RGD:5509061 20111116 MGI PMID:17483418 4141976 Chlq15_m circulating hormone level QTL 15 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:16782841 4141976 Chlq15_m circulating hormone level QTL 15 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16782841 4141977 Mtgq3_m multiple trait growth QTL 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15457339 4141977 Mtgq3_m multiple trait growth QTL 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4141977 Mtgq3_m multiple trait growth QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339|PMID:17517159 4141978 Psds3_m psoriasis-like skin disease severity 3 (mouse) qtl MP:0001193 psoriasis IAGP N RGD:5509061 20111116 MGI PMID:17709541 4141978 Psds3_m psoriasis-like skin disease severity 3 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17709541 4141980 Tcq2_m total cholesterol QTL 2 (mouse) qtl MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:17110492 4141980 Tcq2_m total cholesterol QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4141982 Skts-fp2_m skin tumor susceptibility in FVB and PWK 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17598916 4141982 Skts-fp2_m skin tumor susceptibility in FVB and PWK 2 (mouse) qtl MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20111116 MGI PMID:17598916 4141982 Skts-fp2_m skin tumor susceptibility in FVB and PWK 2 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17598916 4141983 Drinkwater1_m drink water 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141983 Drinkwater1_m drink water 1 (mouse) qtl MP:0011941 increased fluid intake IAGP N RGD:5509061 20130503 MGI PMID:18363849 4141985 Nhil2_m non-heme iron levels 2 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16799992 4141985 Nhil2_m non-heme iron levels 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16799992 4141985 Nhil2_m non-heme iron levels 2 (mouse) qtl MP:0008807 increased liver iron level IAGP N RGD:5509061 20111116 MGI PMID:16799992 4141986 Mskt3_m musculoskeletal traits 3 (mouse) qtl MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141986 Mskt3_m musculoskeletal traits 3 (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20111116 MGI PMID:15824847 4141986 Mskt3_m musculoskeletal traits 3 (mouse) qtl MP:0004348 long femur IAGP N RGD:5509061 20181018 MGI PMID:15824847 4141986 Mskt3_m musculoskeletal traits 3 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141986 Mskt3_m musculoskeletal traits 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141986 Mskt3_m musculoskeletal traits 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4141991 Albq1_m albuminuria QTL 1 (mouse) qtl MP:0002871 albuminuria IAGP N RGD:5509061 20111116 MGI PMID:18493081 4141991 Albq1_m albuminuria QTL 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18493081 4141991 Albq1_m albuminuria QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18493081 4141992 W6q16_m weight 6 weeks QTL 16 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4141992 W6q16_m weight 6 weeks QTL 16 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4141993 Dbmc2_m diabetes mRNA cluster 2 (mouse) qtl MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20111116 MGI PMID:12930764 4141993 Dbmc2_m diabetes mRNA cluster 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12930764 4141996 Drinkcacl21_m drink calcium chloride 2 1 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4141996 Drinkcacl21_m drink calcium chloride 2 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4141997 Bmgr3_m bone marrow graft rejection 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17114464 4141997 Bmgr3_m bone marrow graft rejection 3 (mouse) qtl MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20111116 MGI PMID:17114464 4141998 Hdlq39_m HDL QTL 39 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16685081 4141999 Sfp1_m short free-running period 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19173005 4141999 Sfp1_m short free-running period 1 (mouse) qtl MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:19173005 4142001 Belr1_m berghei liver resistance 1 (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:18365019 4142001 Belr1_m berghei liver resistance 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18365019 4142003 W3q10_m weight 3 weeks QTL 10 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142003 W3q10_m weight 3 weeks QTL 10 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142005 Elpt2_m elevated leptin 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561960 4142005 Elpt2_m elevated leptin 2 (mouse) qtl MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20111116 MGI PMID:15561960 4142007 Chlq17_m circulating hormone level QTL 17 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:16782841 4142007 Chlq17_m circulating hormone level QTL 17 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16782841 4142008 Hdlq58_m HDL QTL 58 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18772481 4142008 Hdlq58_m HDL QTL 58 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18772481 4142009 Pregq3_m pregnancy QTL 3 (mouse) qtl MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20111116 MGI PMID:16547111 4142009 Pregq3_m pregnancy QTL 3 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16547111 4142010 Myci1_m myocardial infarction 1 (mouse) qtl MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20111116 MGI PMID:9754557 4142010 Myci1_m myocardial infarction 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9754557 4142010 Myci1_m myocardial infarction 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9754557 4142011 Mssq13_m mandible size and shape QTL 13 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142011 Mssq13_m mandible size and shape QTL 13 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142011 Mssq13_m mandible size and shape QTL 13 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4142012 Nhdlq8_m non-HDL QTL 8 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16685081 4142014 Wbcq5_m white blood cell quantitative locus 5 (mouse) qtl MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:16261417 4142014 Wbcq5_m white blood cell quantitative locus 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4142014 Wbcq5_m white blood cell quantitative locus 5 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4142015 Idd5.3_m insulin dependent diabetes susceptibility 5.3 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:18056379 4142015 Idd5.3_m insulin dependent diabetes susceptibility 5.3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18056379 4142017 mct1_m modifier of curly tail 1 (mouse) qtl MP:0003051 curly tail IAGP N RGD:5509061 20111116 MGI PMID:8575765 4142017 mct1_m modifier of curly tail 1 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8575765 4142018 Dibg1_m diet-induced blood glucose concentration 1 (mouse) qtl MP:0001559 hyperglycemia IAGP N RGD:5509061 20111116 MGI PMID:15561960 4142018 Dibg1_m diet-induced blood glucose concentration 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561960 4142019 Swq6_m spleen weight QTL 6 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:17110492 4142019 Swq6_m spleen weight QTL 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17110492 4142019 Swq6_m spleen weight QTL 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4142019 Swq6_m spleen weight QTL 6 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4142020 Hbdq1_m high bone density QTL 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:17884746 4142020 Hbdq1_m high bone density QTL 1 (mouse) qtl MP:0010123 increased bone mineral content IAGP N RGD:5509061 20111116 MGI PMID:17884746 4142020 Hbdq1_m high bone density QTL 1 (mouse) qtl MP:0013617 increased areal bone mineral density IAGP N RGD:5509061 20220922 MGI PMID:17884746 4142021 Vmmt4_m vertebral morphology and mechanical traits 4 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4142021 Vmmt4_m vertebral morphology and mechanical traits 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4142023 W3q5_m weight 3 weeks QTL 5 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142023 W3q5_m weight 3 weeks QTL 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142024 Azdm1_m Alzheimer's disease modifier 1 (mouse) qtl MP:0000604 amyloidosis IAGP N RGD:5509061 20111116 MGI PMID:16785251 4142024 Azdm1_m Alzheimer's disease modifier 1 (mouse) qtl MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20111116 MGI PMID:16785251 4142024 Azdm1_m Alzheimer's disease modifier 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16785251 4142024 Azdm1_m Alzheimer's disease modifier 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20140718 MGI Created by mouse qtl pipeline PMID:16785251 4142024 Azdm1_m Alzheimer's disease modifier 1 (mouse) qtl MP:0005395 obsolete other phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16785251 4142029 Vmmt14_m vertebral morphology and mechanical traits 14 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4142029 Vmmt14_m vertebral morphology and mechanical traits 14 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4142031 Moen1_m modifier of engrailed QTL 1 (mouse) qtl MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20111116 MGI PMID:16884697 4142031 Moen1_m modifier of engrailed QTL 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16884697 4142032 Mohg4_m modifier of hg 4 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16670015 4142032 Mohg4_m modifier of hg 4 (mouse) qtl MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20111116 MGI PMID:16670015 4142032 Mohg4_m modifier of hg 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16670015 4142032 Mohg4_m modifier of hg 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16670015 4142032 Mohg4_m modifier of hg 4 (mouse) qtl MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16670015 4142033 Plbcq6_m pleiotropic body composition QTL 6 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:18286334 4142033 Plbcq6_m pleiotropic body composition QTL 6 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18286334 4142033 Plbcq6_m pleiotropic body composition QTL 6 (mouse) qtl MP:0003402 decreased liver weight IAGP N RGD:5509061 20111116 MGI PMID:18286334 4142033 Plbcq6_m pleiotropic body composition QTL 6 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18286334 4142033 Plbcq6_m pleiotropic body composition QTL 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18286334 4142033 Plbcq6_m pleiotropic body composition QTL 6 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18286334 4142033 Plbcq6_m pleiotropic body composition QTL 6 (mouse) qtl MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:18288525 4142033 Plbcq6_m pleiotropic body composition QTL 6 (mouse) qtl MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:18288525 4142033 Plbcq6_m pleiotropic body composition QTL 6 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18286334 4142035 Tbt2_m trabecular bone traits 2 (mouse) qtl MP:0003795 abnormal bone structure IAGP N RGD:5509061 20111116 MGI PMID:16869725 4142035 Tbt2_m trabecular bone traits 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16869725 4142039 Dxcp2_m dexamethasone induced cleft palate 2 (mouse) qtl MP:0000111 cleft palate IAGP N RGD:5509061 20111116 MGI PMID:7157197 4142039 Dxcp2_m dexamethasone induced cleft palate 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:7157197 4142039 Dxcp2_m dexamethasone induced cleft palate 2 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7157197 4142039 Dxcp2_m dexamethasone induced cleft palate 2 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7157197 4142040 Slms2_m sensitivity to locomotor stimulants 2 (mouse) qtl MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20111116 MGI PMID:17010097 4142040 Slms2_m sensitivity to locomotor stimulants 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17010097 4142040 Slms2_m sensitivity to locomotor stimulants 2 (mouse) qtl MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20111116 MGI PMID:17010097 4142044 Hdlq41_m HDL QTL 41 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16951076 4142044 Hdlq41_m HDL QTL 41 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16951076 4142045 Obwq2_m obesity and body weight QTL 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4142045 Obwq2_m obesity and body weight QTL 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4142045 Obwq2_m obesity and body weight QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4142045 Obwq2_m obesity and body weight QTL 2 (mouse) qtl MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4142045 Obwq2_m obesity and body weight QTL 2 (mouse) qtl MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4142046 Eppiq2_m elevated prepulse inhibition QTL 2 (mouse) qtl MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20111116 MGI PMID:15998716 4142046 Eppiq2_m elevated prepulse inhibition QTL 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15998716 4142047 Mvwf3_m modifier of von Willebrand factor 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17155961 4142047 Mvwf3_m modifier of von Willebrand factor 3 (mouse) qtl MP:0031165 increased circulating von Willebrand factor level IAGP N RGD:5509061 20201015 MGI PMID:17155961 4142048 Eac3_m ethyl alcohol consumption QTL 3 (mouse) qtl MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:17273929 4142048 Eac3_m ethyl alcohol consumption QTL 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17273929 4142049 Mohg5_m modifier of hg 5 (mouse) qtl MP:0000592 short tail IAGP N RGD:5509061 20111116 MGI PMID:16670015 4142049 Mohg5_m modifier of hg 5 (mouse) qtl MP:0001258 decreased body length IAGP N RGD:5509061 20111116 MGI PMID:16670015 4142049 Mohg5_m modifier of hg 5 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16670015 4142049 Mohg5_m modifier of hg 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16670015 4142050 Hemq3_m hematocrit QTL 3 (mouse) qtl MP:0002608 increased hematocrit IAGP N RGD:5509061 20111116 MGI PMID:16783647 4142050 Hemq3_m hematocrit QTL 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783647 4142051 Fmtq3_m femur mechanical trait QTL 3 (mouse) qtl MP:0004991 decreased bone strength IAGP N RGD:5509061 20111116 MGI PMID:16869724 4142051 Fmtq3_m femur mechanical trait QTL 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16869724 4142054 Drinknacl1_m drink sodium chloride 1 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4142054 Drinknacl1_m drink sodium chloride 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4142055 Elpt3_m elevated leptin 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15561960 4142055 Elpt3_m elevated leptin 3 (mouse) qtl MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20111116 MGI PMID:15561960 4142058 Ctrq1_m C. trachomatis resistance QTL 1 (mouse) qtl MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:16395389 4142058 Ctrq1_m C. trachomatis resistance QTL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16395389 4142060 W3q6_m weight 3 weeks QTL 6 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142060 W3q6_m weight 3 weeks QTL 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142061 Chlq16_m circulating hormone level QTL 16 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:16782841 4142061 Chlq16_m circulating hormone level QTL 16 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16782841 4142064 Tmc1m4_m Tmc1 modifier 4 (mouse) qtl MP:0001967 deafness IAGP N RGD:5509061 20111116 MGI PMID:16648588 4142064 Tmc1m4_m Tmc1 modifier 4 (mouse) qtl MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20111116 MGI PMID:16648588 4142064 Tmc1m4_m Tmc1 modifier 4 (mouse) qtl MP:0005377 hearing/vestibular/ear phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16648588 4142065 Bmd5b_m bone mineral density 5b (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17451375 4142065 Bmd5b_m bone mineral density 5b (mouse) qtl MP:0010875 increased bone volume IAGP N RGD:5509061 20220922 MGI PMID:17451375 4142066 Gutl1_m gut length 1 (mouse) qtl MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20111116 MGI PMID:17028340 4142066 Gutl1_m gut length 1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17028340 4142067 Ath27_m atherosclerosis 27 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16373612 4142067 Ath27_m atherosclerosis 27 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16373612 4142069 Mssq8_m mandible size and shape QTL 8 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142069 Mssq8_m mandible size and shape QTL 8 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142069 Mssq8_m mandible size and shape QTL 8 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4142070 Vactq2_m voluntary activity QTL 2 (mouse) qtl MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20111116 MGI PMID:18171721 4142070 Vactq2_m voluntary activity QTL 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18171721 4142071 Sh2_m sperm hammerhead 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17483418 4142071 Sh2_m sperm hammerhead 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17483418 4142071 Sh2_m sperm hammerhead 2 (mouse) qtl MP:0005578 teratozoospermia IAGP N RGD:5509061 20111116 MGI PMID:17483418 4142072 Brwq1_m brain weight QTL 1 (mouse) qtl MP:0002175 decreased brain weight IAGP N RGD:5509061 20111116 MGI PMID:17110492 4142072 Brwq1_m brain weight QTL 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4142073 Fbrwt2_m forebrain weight 2 (mouse) qtl MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20111116 MGI PMID:18817551 4142073 Fbrwt2_m forebrain weight 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18817551 4142074 Tmevp2_m Theiler's murine encephalomyelitis virus persistence 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10224268 4142074 Tmevp2_m Theiler's murine encephalomyelitis virus persistence 2 (mouse) qtl MP:0020938 decreased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:10224268 4142077 Ignpq2_m IgA nephropathy QTL 2 (mouse) qtl MP:0002495 increased IgA level IAGP N RGD:5509061 20111116 MGI PMID:16316328 4142077 Ignpq2_m IgA nephropathy QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16316328 4142077 Ignpq2_m IgA nephropathy QTL 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:16316328 4142078 Albq8_m albuminuria QTL 8 (mouse) qtl MP:0002871 albuminuria IAGP N RGD:5509061 20111116 MGI PMID:17804484 4142078 Albq8_m albuminuria QTL 8 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17804484 4142078 Albq8_m albuminuria QTL 8 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17804484 4142079 Skmw15_m skeletal muscle weight 15 (mouse) qtl MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20111116 MGI PMID:16783642 4142079 Skmw15_m skeletal muscle weight 15 (mouse) qtl MP:0003397 increased muscle weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 4142079 Skmw15_m skeletal muscle weight 15 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783642 4142079 Skmw15_m skeletal muscle weight 15 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16783642 4142080 Mpdk8_m modifier of polycystic kidney disease 8 (mouse) qtl MP:0003254 bile duct inflammation IAGP N RGD:5509061 20111116 MGI PMID:15728779 4142080 Mpdk8_m modifier of polycystic kidney disease 8 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15728779 4142080 Mpdk8_m modifier of polycystic kidney disease 8 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15728779 4142081 W10q15_m weight 10 weeks QTL 15 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142081 W10q15_m weight 10 weeks QTL 15 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142083 Ignpq3_m IgA nephropathy QTL 3 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:16316328 4142083 Ignpq3_m IgA nephropathy QTL 3 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16316328 4142083 Ignpq3_m IgA nephropathy QTL 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16316328 4142083 Ignpq3_m IgA nephropathy QTL 3 (mouse) qtl MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:16316328 4142084 Rafar2_m retinoic acid induced forelimb autopod reduction 2 (mouse) qtl MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20111116 MGI PMID:15781699 4142084 Rafar2_m retinoic acid induced forelimb autopod reduction 2 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15781699 4142085 Ctpr1_m citalopram responsiveness 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16554742 4142085 Ctpr1_m citalopram responsiveness 1 (mouse) qtl MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20111116 MGI PMID:16554742 4142086 Vgot1_m vaginal opening timing 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15284200 4142086 Vgot1_m vaginal opening timing 1 (mouse) qtl MP:0008994 early vaginal opening IAGP N RGD:5509061 20111116 MGI PMID:15284200 4142086 Vgot1_m vaginal opening timing 1 (mouse) qtl MP:0008994 early vaginal opening IAGP N RGD:5509061 20111116 MGI PMID:16873534 4142087 W6q7_m weight 6 weeks QTL 7 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142087 W6q7_m weight 6 weeks QTL 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142088 Parms1_m patched associated RMS 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15475264 4142088 Parms1_m patched associated RMS 1 (mouse) qtl MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20111116 MGI PMID:15475264 4142088 Parms1_m patched associated RMS 1 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15475264 4142090 Drinkcala3_m drink calcium lactate 3 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4142090 Drinkcala3_m drink calcium lactate 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4142090 Drinkcala3_m drink calcium lactate 3 (mouse) qtl MP:0011941 increased fluid intake IAGP N RGD:5509061 20130503 MGI PMID:18363849 4142092 Tgq13_m triglyceride QTL 13 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4142092 Tgq13_m triglyceride QTL 13 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4142093 Tcdel1_m T cell clonal deletion 1 (mouse) qtl MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20111116 MGI PMID:15780994 4142093 Tcdel1_m T cell clonal deletion 1 (mouse) qtl MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20111116 MGI PMID:15780994 4142093 Tcdel1_m T cell clonal deletion 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15780994 4142093 Tcdel1_m T cell clonal deletion 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15780994 4142093 Tcdel1_m T cell clonal deletion 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15780994 4142097 Hdlq46_m HDL QTL 46 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16951076 4142097 Hdlq46_m HDL QTL 46 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16951076 4142099 Cq3_m cholesterol QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:10101257 4142101 Albq2_m albuminuria QTL 2 (mouse) qtl MP:0002871 albuminuria IAGP N RGD:5509061 20111116 MGI PMID:18493081 4142101 Albq2_m albuminuria QTL 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18493081 4142101 Albq2_m albuminuria QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18493081 4142102 Tailq5_m tail length QTL 5 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142102 Tailq5_m tail length QTL 5 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142104 Hdlq36_m HDL QTL 36 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16685081 4142105 Lbca2_m LPS-induced B cell activation 2 (mouse) qtl MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:16982900 4142105 Lbca2_m LPS-induced B cell activation 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16982900 4142105 Lbca2_m LPS-induced B cell activation 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16982900 4142105 Lbca2_m LPS-induced B cell activation 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16982900 4142105 Lbca2_m LPS-induced B cell activation 2 (mouse) qtl MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20111116 MGI PMID:16982900 4142108 Psrs7_m psoriasis susceptibility 7 (mouse) qtl MP:0001193 psoriasis IAGP N RGD:5509061 20111116 MGI PMID:16982899 4142108 Psrs7_m psoriasis susceptibility 7 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16982899 4142109 W10q2_m weight 10 weeks QTL 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142109 W10q2_m weight 10 weeks QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142110 Drinkkcl1_m drink potassium chloride 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4142110 Drinkkcl1_m drink potassium chloride 1 (mouse) qtl MP:0011941 increased fluid intake IAGP N RGD:5509061 20130503 MGI PMID:18363849 4142111 Obrq17_m obesity resistance QTL 17 (mouse) qtl MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:19137372 4142111 Obrq17_m obesity resistance QTL 17 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19137372 4142112 Skts-fp3_m skin tumor susceptibility in FVB and PWK 3 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17598916 4142112 Skts-fp3_m skin tumor susceptibility in FVB and PWK 3 (mouse) qtl MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20111116 MGI PMID:17598916 4142112 Skts-fp3_m skin tumor susceptibility in FVB and PWK 3 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17598916 4142113 Pis1_m pilocarpine-induced seizures 1 (mouse) qtl MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20111116 MGI PMID:17242861 4142113 Pis1_m pilocarpine-induced seizures 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17242861 4142113 Pis1_m pilocarpine-induced seizures 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17242861 4142114 Arrd4_m age-related retinal degeneration 4 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17277741 4142114 Arrd4_m age-related retinal degeneration 4 (mouse) qtl MP:0031605 decreased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:17277741 4142115 Fcs3_m fibroblast cell senescence 3 (mouse) qtl MP:0000351 increased cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:16842493 4142115 Fcs3_m fibroblast cell senescence 3 (mouse) qtl MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:16842493 4142115 Fcs3_m fibroblast cell senescence 3 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16842493 4142116 Lsq1_m loss of tissue after ischemia QTL 1 (mouse) qtl MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20111116 MGI PMID:18285563 4142116 Lsq1_m loss of tissue after ischemia QTL 1 (mouse) qtl MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20111116 MGI PMID:18285563 4142116 Lsq1_m loss of tissue after ischemia QTL 1 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18285563 4142116 Lsq1_m loss of tissue after ischemia QTL 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18285563 4142116 Lsq1_m loss of tissue after ischemia QTL 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18285563 4142117 Plbcq7_m pleiotropic body composition QTL 7 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:18286334 4142117 Plbcq7_m pleiotropic body composition QTL 7 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:18286334 4142117 Plbcq7_m pleiotropic body composition QTL 7 (mouse) qtl MP:0003960 increased lean body mass IAGP N RGD:5509061 20111116 MGI PMID:18286334 4142117 Plbcq7_m pleiotropic body composition QTL 7 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18286334 4142117 Plbcq7_m pleiotropic body composition QTL 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18286334 4142121 Tmc1m2_m Tmc1 modifier 2 (mouse) qtl MP:0001967 deafness IAGP N RGD:5509061 20111116 MGI PMID:16648588 4142121 Tmc1m2_m Tmc1 modifier 2 (mouse) qtl MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20111116 MGI PMID:16648588 4142121 Tmc1m2_m Tmc1 modifier 2 (mouse) qtl MP:0005377 hearing/vestibular/ear phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16648588 4142122 Vmmt15_m vertebral morphology and mechanical traits 15 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4142122 Vmmt15_m vertebral morphology and mechanical traits 15 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4142123 Vmmt7_m vertebral morphology and mechanical traits 7 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4142123 Vmmt7_m vertebral morphology and mechanical traits 7 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4142124 Pscr1_m corneal resistance to P. aeruginosa 1 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:3674828 4142124 Pscr1_m corneal resistance to P. aeruginosa 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:3674828 4142126 W3q3_m weight 3 weeks QTL 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142126 W3q3_m weight 3 weeks QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142127 Rafaril_m Rafar interacting locus (mouse) qtl MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20111116 MGI PMID:15781699 4142127 Rafaril_m Rafar interacting locus (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15781699 4142128 Fl1sa_m fatty liver 1 in SMXA (mouse) qtl MP:0001547 abnormal lipid level IAGP N RGD:5509061 20111116 MGI PMID:17595448 4142128 Fl1sa_m fatty liver 1 in SMXA (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:17595448 4142128 Fl1sa_m fatty liver 1 in SMXA (mouse) qtl MP:0003402 decreased liver weight IAGP N RGD:5509061 20111116 MGI PMID:17595448 4142128 Fl1sa_m fatty liver 1 in SMXA (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17595448 4142128 Fl1sa_m fatty liver 1 in SMXA (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17595448 4142128 Fl1sa_m fatty liver 1 in SMXA (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17595448 4142128 Fl1sa_m fatty liver 1 in SMXA (mouse) qtl MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:17595448 4142128 Fl1sa_m fatty liver 1 in SMXA (mouse) qtl MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:17595448 4142128 Fl1sa_m fatty liver 1 in SMXA (mouse) qtl MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:17595448 4142129 Rgv1_m resistance to Gross virus 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:5919331 4142129 Rgv1_m resistance to Gross virus 1 (mouse) qtl MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20111116 MGI PMID:5919331 4142129 Rgv1_m resistance to Gross virus 1 (mouse) qtl MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20111116 MGI PMID:5919331 4142130 Pgis2_m proteoglycan induced spondylitis 2 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:16081819 4142130 Pgis2_m proteoglycan induced spondylitis 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16081819 4142130 Pgis2_m proteoglycan induced spondylitis 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16081819 4142131 Idd5.2_m insulin dependent diabetes susceptibility 5.2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11016460 4142131 Idd5.2_m insulin dependent diabetes susceptibility 5.2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11016460 4142131 Idd5.2_m insulin dependent diabetes susceptibility 5.2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11016460 4142132 Ahl6_m age-related hearing loss 6 (mouse) qtl MP:0005377 hearing/vestibular/ear phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16426780 4142132 Ahl6_m age-related hearing loss 6 (mouse) qtl MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20130503 MGI PMID:16426780 4142133 Pbwg1.6_m postnatal body weight growth 1.6 (mouse) qtl MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20111116 MGI PMID:17514348 4142133 Pbwg1.6_m postnatal body weight growth 1.6 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17514348 4142139 Adip12_m adiposity 12 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4142139 Adip12_m adiposity 12 (mouse) qtl MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4142140 Guq2_m glucosuria QTL 2 (mouse) qtl MP:0001759 increased urine glucose level IAGP N RGD:5509061 20111116 MGI PMID:18227763 4142140 Guq2_m glucosuria QTL 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18227763 4142140 Guq2_m glucosuria QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18227763 4142141 Mtbcq8_m multiple trait body composition QTL 8 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15457339 4142141 Mtbcq8_m multiple trait body composition QTL 8 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4142141 Mtbcq8_m multiple trait body composition QTL 8 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 4142145 Wg7_m weight gain in high growth mice 7 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:17110492 4142145 Wg7_m weight gain in high growth mice 7 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:17110492 4142145 Wg7_m weight gain in high growth mice 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4142146 Eppiq1_m elevated prepulse inhibition QTL 1 (mouse) qtl MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20111116 MGI PMID:15998716 4142146 Eppiq1_m elevated prepulse inhibition QTL 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15998716 4142147 Mvwf4_m modifier of von Willebrand factor 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17155961 4142147 Mvwf4_m modifier of von Willebrand factor 4 (mouse) qtl MP:0031165 increased circulating von Willebrand factor level IAGP N RGD:5509061 20201015 MGI PMID:17155961 4142148 Ckdbp2_m chronic kidney disease blood pressure locus 2 (mouse) qtl MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20111116 MGI PMID:17851470 4142148 Ckdbp2_m chronic kidney disease blood pressure locus 2 (mouse) qtl MP:0002871 albuminuria IAGP N RGD:5509061 20111116 MGI PMID:17851470 4142148 Ckdbp2_m chronic kidney disease blood pressure locus 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17851470 4142148 Ckdbp2_m chronic kidney disease blood pressure locus 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17851470 4142148 Ckdbp2_m chronic kidney disease blood pressure locus 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17851470 4142150 Stheal11_m soft tissue heal 11 (mouse) qtl MP:0002724 enhanced wound healing IAGP N RGD:5509061 20111116 MGI PMID:16341671 4142150 Stheal11_m soft tissue heal 11 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16341671 4142151 Chlq1_m circulating hormone level QTL 1 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:12865502 4142151 Chlq1_m circulating hormone level QTL 1 (mouse) qtl MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20111116 MGI PMID:12865502 4142151 Chlq1_m circulating hormone level QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12865502 4142152 Lspcq1_m low sperm count QTL 1 (mouse) qtl MP:0002687 oligozoospermia IAGP N RGD:5509061 20111116 MGI PMID:18689897 4142152 Lspcq1_m low sperm count QTL 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18689897 4142152 Lspcq1_m low sperm count QTL 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18689897 4142153 Idd21.1_m insulin dependent diabetes susceptibility 21.1 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:16123376 4142153 Idd21.1_m insulin dependent diabetes susceptibility 21.1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16123376 4142154 Mmom1_m mammary modifier of Min 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18056448 4142154 Mmom1_m mammary modifier of Min 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18056448 4142154 Mmom1_m mammary modifier of Min 1 (mouse) qtl MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:18056448 4142154 Mmom1_m mammary modifier of Min 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18056448 4142155 Lmr19_m leishmaniasis resistance 19 (mouse) qtl MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20111116 MGI PMID:16511555 4142155 Lmr19_m leishmaniasis resistance 19 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16511555 4142155 Lmr19_m leishmaniasis resistance 19 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16511555 4142155 Lmr19_m leishmaniasis resistance 19 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16511555 4142157 Azdm2_m Alzheimer's disease modifier 2 (mouse) qtl MP:0000604 amyloidosis IAGP N RGD:5509061 20111116 MGI PMID:16785251 4142157 Azdm2_m Alzheimer's disease modifier 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20140718 MGI Created by mouse qtl pipeline PMID:16785251 4142157 Azdm2_m Alzheimer's disease modifier 2 (mouse) qtl MP:0005395 obsolete other phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16785251 4142159 Nba2_m New Zealand Black autoimmunity 2 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15634937|PMID:10903778 4142159 Nba2_m New Zealand Black autoimmunity 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15634937|PMID:10903778 4142159 Nba2_m New Zealand Black autoimmunity 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15634937|PMID:10903778 4142161 Drinksac2_m drink saccharin 2 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4142161 Drinksac2_m drink saccharin 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4142162 Cia34_m collagen induced arthritis 34 (mouse) qtl MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17312155 4142162 Cia34_m collagen induced arthritis 34 (mouse) qtl MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:17312155 4142162 Cia34_m collagen induced arthritis 34 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17312155 4142162 Cia34_m collagen induced arthritis 34 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17312155 4142163 Ascla5_m atherosclerotic lesion area 5 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16380418 4142163 Ascla5_m atherosclerotic lesion area 5 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16380418 4142165 Imab_m intermale aggressive behavior (mouse) qtl MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20111116 MGI PMID:8138160 4142165 Imab_m intermale aggressive behavior (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8138160 4142169 Pbwg16_m postnatal body weight growth 16 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 4142169 Pbwg16_m postnatal body weight growth 16 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16174331 4142170 Tmrb1_m trace metal regulation in brain 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18189309 4142170 Tmrb1_m trace metal regulation in brain 1 (mouse) qtl MP:0003951 abnormal copper homeostasis IAGP N RGD:5509061 20111116 MGI PMID:18189309 4142170 Tmrb1_m trace metal regulation in brain 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18189309 4142170 Tmrb1_m trace metal regulation in brain 1 (mouse) qtl MP:0008811 abnormal brain iron level IAGP N RGD:5509061 20111116 MGI PMID:18189309 4142171 Lyr3_m lymphoma resistance 3 (mouse) qtl MP:0002879 increased cellular sensitivity to X-ray irradiation IAGP N RGD:5509061 20111116 MGI PMID:7830261 4142171 Lyr3_m lymphoma resistance 3 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7830261 4142172 Arrh3_m arrhythmicity 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19173005 4142172 Arrh3_m arrhythmicity 3 (mouse) qtl MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:19173005 4142173 Mssq18_m mandible size and shape QTL 18 (mouse) qtl MP:0004592 small mandible IAGP N RGD:5509061 20111116 MGI PMID:19067046 4142173 Mssq18_m mandible size and shape QTL 18 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142173 Mssq18_m mandible size and shape QTL 18 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142173 Mssq18_m mandible size and shape QTL 18 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4142174 Nhdlq12_m non-HDL QTL 12 (mouse) qtl MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18048852 4142174 Nhdlq12_m non-HDL QTL 12 (mouse) qtl MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18048852 4142174 Nhdlq12_m non-HDL QTL 12 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18048852 4142175 Pctm_m plasmacytoma modifier (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8105477 4142175 Pctm_m plasmacytoma modifier (mouse) qtl MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20111116 MGI PMID:8105477 4142175 Pctm_m plasmacytoma modifier (mouse) qtl MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20111116 MGI PMID:8105477 4142175 Pctm_m plasmacytoma modifier (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8105477 4142175 Pctm_m plasmacytoma modifier (mouse) qtl MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8105477 4142176 Axtofd5_m anxiety-open field defecation 5 (mouse) qtl MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20160519 MGI PMID:14990867 4142176 Axtofd5_m anxiety-open field defecation 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14990867 4142176 Axtofd5_m anxiety-open field defecation 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20160513 MGI Created by mouse qtl pipeline PMID:11454769 4142178 Ctrq2_m C. trachomatis resistance QTL 2 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:16395389 4142178 Ctrq2_m C. trachomatis resistance QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16395389 4142179 Hdlq33_m HDL QTL 33 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16685081 4142179 Hdlq33_m HDL QTL 33 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16685081 4142180 Nicoq4_m nicotine consumption QTL 4 (mouse) qtl MP:0002553 preference for addictive substance IAGP N RGD:5509061 20111116 MGI PMID:17010155 4142180 Nicoq4_m nicotine consumption QTL 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17010155 4142181 Slpd1_m susceptibility to lymphoproliferative disease 1 (mouse) qtl MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:17351108 4142181 Slpd1_m susceptibility to lymphoproliferative disease 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17351108 4142181 Slpd1_m susceptibility to lymphoproliferative disease 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17351108 4142181 Slpd1_m susceptibility to lymphoproliferative disease 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17351108 4142182 Shali5_m survival time to hyperoxic acute lung injury 5 (mouse) qtl MP:0003674 oxidative stress IAGP N RGD:5509061 20111116 MGI PMID:17488888 4142182 Shali5_m survival time to hyperoxic acute lung injury 5 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17488888 4142184 Mcvq2_m mean corpuscular volume QTL 2 (mouse) qtl MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20111116 MGI PMID:16596451 4142184 Mcvq2_m mean corpuscular volume QTL 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16596451 4142185 Pbwg1.3_m postnatal body weight growth 1.3 (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20111116 MGI PMID:17514348 4142185 Pbwg1.3_m postnatal body weight growth 1.3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17514348 4142187 Arrd3_m age-related retinal degeneration 3 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12766041 4142187 Arrd3_m age-related retinal degeneration 3 (mouse) qtl MP:0031605 decreased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:12766041 4142188 Mskt6_m musculoskeletal traits 6 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:15824847 4142188 Mskt6_m musculoskeletal traits 6 (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20111116 MGI PMID:15824847 4142188 Mskt6_m musculoskeletal traits 6 (mouse) qtl MP:0004348 long femur IAGP N RGD:5509061 20181018 MGI PMID:15824847 4142188 Mskt6_m musculoskeletal traits 6 (mouse) qtl MP:0004357 long tibia IAGP N RGD:5509061 20181018 MGI PMID:15824847 4142188 Mskt6_m musculoskeletal traits 6 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4142188 Mskt6_m musculoskeletal traits 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4142188 Mskt6_m musculoskeletal traits 6 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4142189 Adre_m age at disappearance of rooting response (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:4080829 4142189 Adre_m age at disappearance of rooting response (mouse) qtl MP:0020864 premature suckling reflex loss IAGP N RGD:5509061 20220922 MGI PMID:3426502 4142189 Adre_m age at disappearance of rooting response (mouse) qtl MP:0020864 premature suckling reflex loss IAGP N RGD:5509061 20220922 MGI PMID:4080829 4142189 Adre_m age at disappearance of rooting response (mouse) qtl MP:0020865 delayed suckling reflex loss IAGP N RGD:5509061 20220922 MGI PMID:3426502 4142190 Lskpf1_m LSK cell population frequency 1 (mouse) qtl MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20111116 MGI PMID:18288524 4142190 Lskpf1_m LSK cell population frequency 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18288524 4142191 Lwq9_m liver weight QTL 9 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:17110492 4142191 Lwq9_m liver weight QTL 9 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4142191 Lwq9_m liver weight QTL 9 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17110492 4142192 Obrq14_m obesity resistance QTL 14 (mouse) qtl MP:0002628 hepatic steatosis IAGP N RGD:5509061 20111116 MGI PMID:19137372 4142192 Obrq14_m obesity resistance QTL 14 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:19137372 4142192 Obrq14_m obesity resistance QTL 14 (mouse) qtl MP:0005331 insulin resistance IAGP N RGD:5509061 20111116 MGI PMID:19137372 4142192 Obrq14_m obesity resistance QTL 14 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19137372 4142192 Obrq14_m obesity resistance QTL 14 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19137372 4142192 Obrq14_m obesity resistance QTL 14 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19137372 4142192 Obrq14_m obesity resistance QTL 14 (mouse) qtl MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20111116 MGI PMID:19137372 4142194 Plbcq8_m pleiotropic body composition QTL 8 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:18286334 4142194 Plbcq8_m pleiotropic body composition QTL 8 (mouse) qtl MP:0003960 increased lean body mass IAGP N RGD:5509061 20111116 MGI PMID:18286334 4142194 Plbcq8_m pleiotropic body composition QTL 8 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18286334 4142194 Plbcq8_m pleiotropic body composition QTL 8 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18286334 4142194 Plbcq8_m pleiotropic body composition QTL 8 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:18286334 4142196 W10q4_m weight 10 weeks QTL 4 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142196 W10q4_m weight 10 weeks QTL 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142198 Hbtq_m habituation QTL (mouse) qtl MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20111116 MGI PMID:14561872 4142198 Hbtq_m habituation QTL (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14561872 4142199 Poats1_m post-ovarectomy adrenal tumor susceptibility 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18006632 4142199 Poats1_m post-ovarectomy adrenal tumor susceptibility 1 (mouse) qtl MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:18006632 4142199 Poats1_m post-ovarectomy adrenal tumor susceptibility 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18006632 4142200 Rtwq1_m reduced testis weight QTL 1 (mouse) qtl MP:0004852 decreased testis weight IAGP N RGD:5509061 20111116 MGI PMID:18689897 4142200 Rtwq1_m reduced testis weight QTL 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18689897 4142200 Rtwq1_m reduced testis weight QTL 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18689897 4142201 Obrq15_m obesity resistance QTL 15 (mouse) qtl MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20111116 MGI PMID:19137372 4142201 Obrq15_m obesity resistance QTL 15 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19137372 4142201 Obrq15_m obesity resistance QTL 15 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19137372 4142201 Obrq15_m obesity resistance QTL 15 (mouse) qtl MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20111116 MGI PMID:19137372 4142202 Feml4_m femur length in high growth mice 4 (mouse) qtl MP:0003109 short femur IAGP N RGD:5509061 20111116 MGI PMID:17110492 4142202 Feml4_m femur length in high growth mice 4 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4142202 Feml4_m femur length in high growth mice 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4142203 Lyr_m lymphoma resistance (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:2354437 4142203 Lyr_m lymphoma resistance (mouse) qtl MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20111116 MGI PMID:2354437 4142203 Lyr_m lymphoma resistance (mouse) qtl MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20111116 MGI PMID:2354437 4142203 Lyr_m lymphoma resistance (mouse) qtl MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20131227 MGI PMID:2354437 4142205 Drinksac5_m drink saccharin 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4142205 Drinksac5_m drink saccharin 5 (mouse) qtl MP:0011941 increased fluid intake IAGP N RGD:5509061 20130503 MGI PMID:18363849 4142206 Hdlq47_m HDL QTL 47 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16951076 4142206 Hdlq47_m HDL QTL 47 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18772481|PMID:16951076 4142206 Hdlq47_m HDL QTL 47 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:16951076 4142207 Albq3_m albuminuria QTL 3 (mouse) qtl MP:0002871 albuminuria IAGP N RGD:5509061 20111116 MGI PMID:18493081 4142207 Albq3_m albuminuria QTL 3 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18493081 4142207 Albq3_m albuminuria QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18493081 4142209 Psrs1_m psoriasis susceptibility 1 (mouse) qtl MP:0001193 psoriasis IAGP N RGD:5509061 20111116 MGI PMID:16982899 4142209 Psrs1_m psoriasis susceptibility 1 (mouse) qtl MP:0001193 psoriasis IAGP N RGD:5509061 20111116 MGI PMID:18390736 4142209 Psrs1_m psoriasis susceptibility 1 (mouse) qtl MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20111116 MGI PMID:18390736 4142209 Psrs1_m psoriasis susceptibility 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16982899 4142209 Psrs1_m psoriasis susceptibility 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16982899 4142209 Psrs1_m psoriasis susceptibility 1 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16982899 4142210 Ads2_m anti dsDNA antibody 2 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:6864161 4142210 Ads2_m anti dsDNA antibody 2 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20111116 MGI PMID:6864161 4142210 Ads2_m anti dsDNA antibody 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6864161 4142211 Nilac3_m nicotine induced locomotor activity 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16176386 4142211 Nilac3_m nicotine induced locomotor activity 3 (mouse) qtl MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:16176386 4142211 Nilac3_m nicotine induced locomotor activity 3 (mouse) qtl MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:19083055 4142215 W3q9_m weight 3 weeks QTL 9 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142215 W3q9_m weight 3 weeks QTL 9 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142216 Lgq1_m late growth QTL 1 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142216 Lgq1_m late growth QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142217 Tdnq1_m Tgfb1 trangenic F2 between DBA/2 and NOD QTL 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:18160996 4142217 Tdnq1_m Tgfb1 trangenic F2 between DBA/2 and NOD QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18160996 4142218 W6q17_m weight 6 weeks QTL 17 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142218 W6q17_m weight 6 weeks QTL 17 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142219 Egaq1_m early growth adjusted QTL 1 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142219 Egaq1_m early growth adjusted QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142222 Mpdk5_m modifier of polycystic kidney disease 5 (mouse) qtl MP:0002706 abnormal kidney size IAGP N RGD:5509061 20111116 MGI PMID:15728779 4142222 Mpdk5_m modifier of polycystic kidney disease 5 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15728779 4142222 Mpdk5_m modifier of polycystic kidney disease 5 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15728779 4142222 Mpdk5_m modifier of polycystic kidney disease 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15728779 4142224 Cia42_m collagen induced arthritis 42 (mouse) qtl MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17312155 4142224 Cia42_m collagen induced arthritis 42 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17312155 4142224 Cia42_m collagen induced arthritis 42 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17312155 4142225 Chcmq1_m mean cell hemoglobin concentration QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16596451 4142225 Chcmq1_m mean cell hemoglobin concentration QTL 1 (mouse) qtl MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20111116 MGI PMID:16596451 4142228 Adip13_m adiposity 13 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4142228 Adip13_m adiposity 13 (mouse) qtl MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4142230 Azdm3_m Alzheimer's disease modifier 3 (mouse) qtl MP:0000604 amyloidosis IAGP N RGD:5509061 20111116 MGI PMID:16785251 4142230 Azdm3_m Alzheimer's disease modifier 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20140718 MGI Created by mouse qtl pipeline PMID:16785251 4142230 Azdm3_m Alzheimer's disease modifier 3 (mouse) qtl MP:0005395 obsolete other phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16785251 4142231 Pbwg1.9_m postnatal body weight growth 1.9 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:17514348 4142231 Pbwg1.9_m postnatal body weight growth 1.9 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17514348 4142231 Pbwg1.9_m postnatal body weight growth 1.9 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17514348 4142231 Pbwg1.9_m postnatal body weight growth 1.9 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17514348 4142232 W6q4_m weight 6 weeks QTL 4 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142232 W6q4_m weight 6 weeks QTL 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142234 Tmc1m3_m Tmc1 modifier 3 (mouse) qtl MP:0001967 deafness IAGP N RGD:5509061 20111116 MGI PMID:16648588 4142234 Tmc1m3_m Tmc1 modifier 3 (mouse) qtl MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20111116 MGI PMID:16648588 4142234 Tmc1m3_m Tmc1 modifier 3 (mouse) qtl MP:0005377 hearing/vestibular/ear phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16648588 4142237 Pscr2_m corneal resistance to P. aeruginosa 2 (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:3674828 4142237 Pscr2_m corneal resistance to P. aeruginosa 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:3674828 4142239 Idd21.2_m insulin dependent diabetes susceptibility 21.2 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:16123376 4142239 Idd21.2_m insulin dependent diabetes susceptibility 21.2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16123376 4142241 Tailq3_m tail length QTL 3 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142241 Tailq3_m tail length QTL 3 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142242 Drinkcala2_m drink calcium lactate 2 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4142242 Drinkcala2_m drink calcium lactate 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4142246 Qbis4_m QTL for body weight independent of sex 4 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16321990 4142246 Qbis4_m QTL for body weight independent of sex 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16321990 4142247 Ckdbp1_m chronic kidney disease blood pressure locus 1 (mouse) qtl MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20111116 MGI PMID:17851470 4142247 Ckdbp1_m chronic kidney disease blood pressure locus 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17851470 4142249 Ffaq2_m free fatty acid QTL 2 (mouse) qtl MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4142249 Ffaq2_m free fatty acid QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4142250 Idd21.3_m insulin dependent diabetes susceptibility 21.3 (mouse) qtl MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20111116 MGI PMID:16123376 4142250 Idd21.3_m insulin dependent diabetes susceptibility 21.3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16123376 4142251 Sgp1_m serum gp70 production 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6601614 4142251 Sgp1_m serum gp70 production 1 (mouse) qtl MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20111116 MGI PMID:6601614 4142252 Tailaq4_m tail length adjusted QTL 4 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142252 Tailaq4_m tail length adjusted QTL 4 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142254 Pbwg15_m postnatal body weight growth 15 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 4142254 Pbwg15_m postnatal body weight growth 15 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16174331 4142255 Eac1_m ethyl alcohol consumption QTL 1 (mouse) qtl MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20111116 MGI PMID:17273929 4142255 Eac1_m ethyl alcohol consumption QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17273929 4142256 Nilac12_m nicotine induced locomotor activity 12 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16176386 4142256 Nilac12_m nicotine induced locomotor activity 12 (mouse) qtl MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:16176386 4142257 Chlq12_m circulating hormone level QTL 12 (mouse) qtl MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:16782841 4142257 Chlq12_m circulating hormone level QTL 12 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16782841 4142259 Tabw2_m tally ho associated body weight 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15870394 4142259 Tabw2_m tally ho associated body weight 2 (mouse) qtl MP:0005331 insulin resistance IAGP N RGD:5509061 20111116 MGI PMID:15870394 4142259 Tabw2_m tally ho associated body weight 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15870394 4142259 Tabw2_m tally ho associated body weight 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15870394 4142259 Tabw2_m tally ho associated body weight 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15870394 4142259 Tabw2_m tally ho associated body weight 2 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:15870394 4142259 Tabw2_m tally ho associated body weight 2 (mouse) qtl MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20111116 MGI PMID:15870394 4142259 Tabw2_m tally ho associated body weight 2 (mouse) qtl MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:15870394 4142260 Ctl1_m cytotoxic T lymphocyte response 1 (mouse) qtl MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20111116 MGI PMID:6802754 4142260 Ctl1_m cytotoxic T lymphocyte response 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6802754 4142260 Ctl1_m cytotoxic T lymphocyte response 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:6802754 4142261 Gpab1_m gp70 autoantibody titers 1 (mouse) qtl MP:0001844 autoimmune response IAGP N RGD:5509061 20111116 MGI PMID:11466397 4142261 Gpab1_m gp70 autoantibody titers 1 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:11466397 4142261 Gpab1_m gp70 autoantibody titers 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11466397 4142262 Lmr18_m leishmaniasis resistance 18 (mouse) qtl MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20111116 MGI PMID:16511555 4142262 Lmr18_m leishmaniasis resistance 18 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16511555 4142262 Lmr18_m leishmaniasis resistance 18 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16511555 4142262 Lmr18_m leishmaniasis resistance 18 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16511555 4142262 Lmr18_m leishmaniasis resistance 18 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16511555 4142262 Lmr18_m leishmaniasis resistance 18 (mouse) qtl MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20111116 MGI PMID:16511555 4142263 Obwq4_m obesity and body weight QTL 4 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4142263 Obwq4_m obesity and body weight QTL 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4142263 Obwq4_m obesity and body weight QTL 4 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4142263 Obwq4_m obesity and body weight QTL 4 (mouse) qtl MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4142263 Obwq4_m obesity and body weight QTL 4 (mouse) qtl MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4142263 Obwq4_m obesity and body weight QTL 4 (mouse) qtl MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4142263 Obwq4_m obesity and body weight QTL 4 (mouse) qtl MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4142264 Hgbq1_m hemoglobin QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16596451 4142264 Hgbq1_m hemoglobin QTL 1 (mouse) qtl MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20111116 MGI PMID:16596451 4142266 Ascla6_m atherosclerotic lesion area 6 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16380418 4142266 Ascla6_m atherosclerotic lesion area 6 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16380418 4142267 Cmn3_m cardiac modifier of nmd 3 (mouse) qtl MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20111116 MGI PMID:16174646 4142267 Cmn3_m cardiac modifier of nmd 3 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16174646 4142267 Cmn3_m cardiac modifier of nmd 3 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16174646 4142268 Agp1_m anti gp70 immune complex 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6217253 4142268 Agp1_m anti gp70 immune complex 1 (mouse) qtl MP:0005615 increased susceptibility to type III hypersensitivity reaction IAGP N RGD:5509061 20111116 MGI PMID:6217253 4142271 Egq8_m early growth QTL 8 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142271 Egq8_m early growth QTL 8 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142272 W10q5_m weight 10 weeks QTL 5 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142272 W10q5_m weight 10 weeks QTL 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142273 Hrdg1_m hyperoxia-induced retinal degeneration 1 (mouse) qtl MP:0001326 retina degeneration IAGP N RGD:5509061 20111116 MGI PMID:17197561 4142273 Hrdg1_m hyperoxia-induced retinal degeneration 1 (mouse) qtl MP:0003455 decreased susceptibility to induced retina damage IAGP N RGD:5509061 20240404 MGI PMID:17197561 4142273 Hrdg1_m hyperoxia-induced retinal degeneration 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17197561 4142274 Plast1_m plasma plant sterol 1 (mouse) qtl MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:12446833 4142274 Plast1_m plasma plant sterol 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12446833 4142275 Secia2_m small effect CIA locus 2 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17244351 4142275 Secia2_m small effect CIA locus 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4142275 Secia2_m small effect CIA locus 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4142277 Bglu9_m blood glucose level 9 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18362393 4142277 Bglu9_m blood glucose level 9 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:18362393 4142278 Mtbcq3_m multiple trait body composition QTL 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4142278 Mtbcq3_m multiple trait body composition QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4142279 Tilss3_m TNF-induced lethal shock susceptibility 3 (mouse) qtl MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20111116 MGI PMID:17404289 4142279 Tilss3_m TNF-induced lethal shock susceptibility 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17404289 4142280 Shali4_m survival time to hyperoxic acute lung injury 4 (mouse) qtl MP:0003674 oxidative stress IAGP N RGD:5509061 20111116 MGI PMID:17488888 4142280 Shali4_m survival time to hyperoxic acute lung injury 4 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17488888 4142281 Chlq2_m circulating hormone level QTL 2 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:12865502 4142281 Chlq2_m circulating hormone level QTL 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12865502 4142283 Imraq2_m immune response to AAV2 QTL 2 (mouse) qtl MP:0002493 increased IgG level IAGP N RGD:5509061 20111116 MGI PMID:15922957 4142283 Imraq2_m immune response to AAV2 QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15922957 4142283 Imraq2_m immune response to AAV2 QTL 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:15922957 4142284 Sfp2_m short free-running period 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19173005 4142284 Sfp2_m short free-running period 2 (mouse) qtl MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:19173005 4142286 Pubt1_m pubertal timing 1 (mouse) qtl MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20111116 MGI PMID:18725948 4142286 Pubt1_m pubertal timing 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18725948 4142287 Hfem4_m Hfe modifier 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15131800 4142287 Hfem4_m Hfe modifier 4 (mouse) qtl MP:0005638 hemochromatosis IAGP N RGD:5509061 20111116 MGI PMID:15131800 4142288 Mcvq1_m mean corpuscular volume QTL 1 (mouse) qtl MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20111116 MGI PMID:16596451 4142288 Mcvq1_m mean corpuscular volume QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16596451 4142289 Mskt5_m musculoskeletal traits 5 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:15824847 4142289 Mskt5_m musculoskeletal traits 5 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15824847 4142289 Mskt5_m musculoskeletal traits 5 (mouse) qtl MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20111116 MGI PMID:15824847 4142289 Mskt5_m musculoskeletal traits 5 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4142289 Mskt5_m musculoskeletal traits 5 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4142289 Mskt5_m musculoskeletal traits 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4142289 Mskt5_m musculoskeletal traits 5 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4142289 Mskt5_m musculoskeletal traits 5 (mouse) qtl MP:0006087 increased body mass index IAGP N RGD:5509061 20111116 MGI PMID:15824847 4142291 Aec2_m autoimmune exocrinopathy 2 (mouse) qtl MP:0000623 decreased salivation IAGP N RGD:5509061 20111116 MGI PMID:12115247 4142291 Aec2_m autoimmune exocrinopathy 2 (mouse) qtl MP:0000623 decreased salivation IAGP N RGD:5509061 20111116 MGI PMID:12614028 4142291 Aec2_m autoimmune exocrinopathy 2 (mouse) qtl MP:0000623 decreased salivation IAGP N RGD:5509061 20111116 MGI PMID:16918699 4142291 Aec2_m autoimmune exocrinopathy 2 (mouse) qtl MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20111116 MGI PMID:16918699 4142291 Aec2_m autoimmune exocrinopathy 2 (mouse) qtl MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:16918699 4142291 Aec2_m autoimmune exocrinopathy 2 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20111116 MGI PMID:12115247 4142291 Aec2_m autoimmune exocrinopathy 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115247 4142291 Aec2_m autoimmune exocrinopathy 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115247 4142291 Aec2_m autoimmune exocrinopathy 2 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115247 4142291 Aec2_m autoimmune exocrinopathy 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115247 4142291 Aec2_m autoimmune exocrinopathy 2 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115247 4142291 Aec2_m autoimmune exocrinopathy 2 (mouse) qtl MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20111116 MGI PMID:12115247 4142291 Aec2_m autoimmune exocrinopathy 2 (mouse) qtl MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141211 MGI PMID:16918699 4142293 Mssq2_m mandible size and shape QTL 2 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142293 Mssq2_m mandible size and shape QTL 2 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142293 Mssq2_m mandible size and shape QTL 2 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4142294 Ads1_m anti dsDNA antibody 1 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:6642573 4142294 Ads1_m anti dsDNA antibody 1 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:6864161 4142294 Ads1_m anti dsDNA antibody 1 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20111116 MGI PMID:6864161 4142294 Ads1_m anti dsDNA antibody 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6864161 4142295 Mtbcq1_m multiple trait body composition QTL 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15457339 4142295 Mtbcq1_m multiple trait body composition QTL 1 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4142295 Mtbcq1_m multiple trait body composition QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15457339 4142298 Bmd22_m bone mineral density 22 (mouse) qtl MP:0000062 increased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:16355279 4142298 Bmd22_m bone mineral density 22 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16355279 4142298 Bmd22_m bone mineral density 22 (mouse) qtl MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20220922 MGI PMID:16355279 4142299 Pbwg1.4_m postnatal body weight growth 1.4 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:17514348 4142299 Pbwg1.4_m postnatal body weight growth 1.4 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17514348 4142300 Ctrq3_m C. trachomatis resistance QTL 3 (mouse) qtl MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:16395389 4142300 Ctrq3_m C. trachomatis resistance QTL 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18424746|PMID:16395389 4142301 Mlrrq_m malaria resistance QTL (mouse) qtl MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20111116 MGI PMID:9207740 4142301 Mlrrq_m malaria resistance QTL (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9207740 4142302 Nstr1_m nerve sheath tumor resistance QTL 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16397217 4142302 Nstr1_m nerve sheath tumor resistance QTL 1 (mouse) qtl MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20111116 MGI PMID:16397217 4142302 Nstr1_m nerve sheath tumor resistance QTL 1 (mouse) qtl MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:16397217 4142302 Nstr1_m nerve sheath tumor resistance QTL 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16397217 4142303 Plbcq9_m pleiotropic body composition QTL 9 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:18286334 4142303 Plbcq9_m pleiotropic body composition QTL 9 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18286334 4142304 Hdlq53_m HDL QTL 53 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18772481 4142304 Hdlq53_m HDL QTL 53 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18772481 4142305 Find2_m fat induced diabetes 2 (mouse) qtl MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:15870393 4142305 Find2_m fat induced diabetes 2 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:15870393 4142305 Find2_m fat induced diabetes 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15870393 4142305 Find2_m fat induced diabetes 2 (mouse) qtl MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:15870393 4142307 Shali1_m survival time to hyperoxic acute lung injury 1 (mouse) qtl MP:0003674 oxidative stress IAGP N RGD:5509061 20111116 MGI PMID:17488888 4142307 Shali1_m survival time to hyperoxic acute lung injury 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17488888 4142308 W6q3_m weight 6 weeks QTL 3 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142308 W6q3_m weight 6 weeks QTL 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142309 Ssnt1_m short snout 1 (mouse) qtl MP:0000445 short snout IAGP N RGD:5509061 20111116 MGI PMID:18037656 4142309 Ssnt1_m short snout 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:14530301 4142309 Ssnt1_m short snout 1 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14530301 4142312 Nilac4_m nicotine induced locomotor activity 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16176386 4142312 Nilac4_m nicotine induced locomotor activity 4 (mouse) qtl MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:16176386 4142314 Tailaq3_m tail length adjusted QTL 3 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142314 Tailaq3_m tail length adjusted QTL 3 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142315 Irav1_m immune response to adenovirus 1 (mouse) qtl MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20111116 MGI PMID:17362354 4142315 Irav1_m immune response to adenovirus 1 (mouse) qtl MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20111116 MGI PMID:17362354 4142315 Irav1_m immune response to adenovirus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17362354 4142316 Ity2b_m immunity to S. typhimurium 2b (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:17660555 4142316 Ity2b_m immunity to S. typhimurium 2b (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17660555 4142317 Rgcs1_m retinal ganglion cell susceptible 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18671875 4142317 Rgcs1_m retinal ganglion cell susceptible 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18671875 4142317 Rgcs1_m retinal ganglion cell susceptible 1 (mouse) qtl MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20111116 MGI PMID:18671875 4142318 Lyr2_m lymphoma resistance 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8613427 4142318 Lyr2_m lymphoma resistance 2 (mouse) qtl MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8613427 4142321 Nihlr1_m noise-induced hearing loss resistance 1 (mouse) qtl MP:0004925 decreased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20111116 MGI PMID:19337678 4142321 Nihlr1_m noise-induced hearing loss resistance 1 (mouse) qtl MP:0005377 hearing/vestibular/ear phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19337678 4142322 Albq4_m albuminuria QTL 4 (mouse) qtl MP:0002871 albuminuria IAGP N RGD:5509061 20111116 MGI PMID:18493081 4142322 Albq4_m albuminuria QTL 4 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18493081 4142322 Albq4_m albuminuria QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18493081 4142323 Hdlq38_m HDl QTL 38 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16685081 4142325 Mlca1_m modifier of locomotor activity 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16436185 4142325 Mlca1_m modifier of locomotor activity 1 (mouse) qtl MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:16436185 4142326 Tgq19_m triglyceride QTL 19 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4142326 Tgq19_m triglyceride QTL 19 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4142327 Clptq1_m cellular lupus traits QTL 1 (mouse) qtl MP:0000691 enlarged spleen IAGP N RGD:5509061 20111116 MGI PMID:17237410 4142327 Clptq1_m cellular lupus traits QTL 1 (mouse) qtl MP:0000709 enlarged thymus IAGP N RGD:5509061 20111116 MGI PMID:17237410 4142327 Clptq1_m cellular lupus traits QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17237410 4142327 Clptq1_m cellular lupus traits QTL 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:17237410 4142327 Clptq1_m cellular lupus traits QTL 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17237410 4142327 Clptq1_m cellular lupus traits QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17237410 4142327 Clptq1_m cellular lupus traits QTL 1 (mouse) qtl MP:0008039 increased NK T cell number IAGP N RGD:5509061 20111116 MGI PMID:17237410 4142327 Clptq1_m cellular lupus traits QTL 1 (mouse) qtl MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20111116 MGI PMID:17237410 4142328 Kwq13_m kidney weight QTL 13 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:17110492 4142328 Kwq13_m kidney weight QTL 13 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4142328 Kwq13_m kidney weight QTL 13 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17110492 4142329 Hbnr6_m Heligmosomoides bakeri nematode resistance 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14507332 4142329 Hbnr6_m Heligmosomoides bakeri nematode resistance 6 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:14507332 4142330 Asdq5_m atrial septal defect QTL 5 (mouse) qtl MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20111116 MGI PMID:16484617 4142330 Asdq5_m atrial septal defect QTL 5 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16484617 4142331 Bxs6_m BXSB/MpJ autoimmune nephritis 6 (mouse) qtl MP:0000691 enlarged spleen IAGP N RGD:5509061 20111116 MGI PMID:17371996 4142331 Bxs6_m BXSB/MpJ autoimmune nephritis 6 (mouse) qtl MP:0001844 autoimmune response IAGP N RGD:5509061 20111116 MGI PMID:11466397 4142331 Bxs6_m BXSB/MpJ autoimmune nephritis 6 (mouse) qtl MP:0001844 autoimmune response IAGP N RGD:5509061 20111116 MGI PMID:17371996 4142331 Bxs6_m BXSB/MpJ autoimmune nephritis 6 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:11466397 4142331 Bxs6_m BXSB/MpJ autoimmune nephritis 6 (mouse) qtl MP:0002743 glomerulonephritis IAGP N RGD:5509061 20111116 MGI PMID:17371996 4142331 Bxs6_m BXSB/MpJ autoimmune nephritis 6 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:11466397 4142331 Bxs6_m BXSB/MpJ autoimmune nephritis 6 (mouse) qtl MP:0003725 increased autoantibody level IAGP N RGD:5509061 20111116 MGI PMID:17371996 4142331 Bxs6_m BXSB/MpJ autoimmune nephritis 6 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:17371996 4142331 Bxs6_m BXSB/MpJ autoimmune nephritis 6 (mouse) qtl MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:17371996 4142331 Bxs6_m BXSB/MpJ autoimmune nephritis 6 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17371996 4142331 Bxs6_m BXSB/MpJ autoimmune nephritis 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17371996 4142331 Bxs6_m BXSB/MpJ autoimmune nephritis 6 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17371996 4142331 Bxs6_m BXSB/MpJ autoimmune nephritis 6 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17371996 4142333 Tgq10_m triglyceride QTL 10 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4142333 Tgq10_m triglyceride QTL 10 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4142334 Svtms_m survival time modifier of Sod2 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16497723 4142334 Svtms_m survival time modifier of Sod2 (mouse) qtl MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20111116 MGI PMID:16497723 4142337 Adip10_m adiposity 10 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4142337 Adip10_m adiposity 10 (mouse) qtl MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4142337 Adip10_m adiposity 10 (mouse) qtl MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4142338 Skmw18_m skeletal muscle weight 18 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783642 4142338 Skmw18_m skeletal muscle weight 18 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16783642 4142338 Skmw18_m skeletal muscle weight 18 (mouse) qtl MP:0009425 increased soleus weight IAGP N RGD:5509061 20111116 MGI PMID:16783642 4142339 Spmd3_m spermatogenesis defect 3 (mouse) qtl MP:0002687 oligozoospermia IAGP N RGD:5509061 20111116 MGI PMID:16651692 4142339 Spmd3_m spermatogenesis defect 3 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16651692 4142339 Spmd3_m spermatogenesis defect 3 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16651692 4142341 Sgp2_m serum gp70 production 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6629441 4142341 Sgp2_m serum gp70 production 2 (mouse) qtl MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20111116 MGI PMID:6629441 4142343 Moen2_m modifier of engrailed QTL 2 (mouse) qtl MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20111116 MGI PMID:16884697 4142343 Moen2_m modifier of engrailed QTL 2 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16884697 4142349 Hmtb2_m hemostasis and thrombosis 2 (mouse) qtl MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20111116 MGI PMID:17022820 4142349 Hmtb2_m hemostasis and thrombosis 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17022820 4142351 Guq1_m glucosuria QTL 1 (mouse) qtl MP:0001759 increased urine glucose level IAGP N RGD:5509061 20111116 MGI PMID:18227763 4142351 Guq1_m glucosuria QTL 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18227763 4142351 Guq1_m glucosuria QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18227763 4142352 Lmr17_m leishmaniasis resistance 17 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16511555 4142352 Lmr17_m leishmaniasis resistance 17 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16511555 4142352 Lmr17_m leishmaniasis resistance 17 (mouse) qtl MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20111116 MGI PMID:16511555 4142352 Lmr17_m leishmaniasis resistance 17 (mouse) qtl MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20111116 MGI PMID:16511555 4142354 Fl2sa_m fatty liver 2 in SMXA (mouse) qtl MP:0001547 abnormal lipid level IAGP N RGD:5509061 20111116 MGI PMID:17595448 4142354 Fl2sa_m fatty liver 2 in SMXA (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:17595448 4142354 Fl2sa_m fatty liver 2 in SMXA (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17595448 4142354 Fl2sa_m fatty liver 2 in SMXA (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17595448 4142354 Fl2sa_m fatty liver 2 in SMXA (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:17595448 4142355 Chlq3_m circulating hormone level QTL 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12865502 4142355 Chlq3_m circulating hormone level QTL 3 (mouse) qtl MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20111116 MGI PMID:12865502 4142356 Tcdel2_m T cell clonal deletion 2 (mouse) qtl MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20111116 MGI PMID:15780994 4142356 Tcdel2_m T cell clonal deletion 2 (mouse) qtl MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20111116 MGI PMID:15780994 4142356 Tcdel2_m T cell clonal deletion 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15780994 4142356 Tcdel2_m T cell clonal deletion 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15780994 4142356 Tcdel2_m T cell clonal deletion 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15780994 4142358 Fcs2_m fibroblast cell senescence 2 (mouse) qtl MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:16842493 4142358 Fcs2_m fibroblast cell senescence 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16842493 4142359 Mssq16_m mandible size and shape QTL 16 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142359 Mssq16_m mandible size and shape QTL 16 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142359 Mssq16_m mandible size and shape QTL 16 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4142360 Vmmt20_m vertebral morphology and mechanical traits 20 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4142360 Vmmt20_m vertebral morphology and mechanical traits 20 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4142361 W10q11_m weight 10 weeks QTL 11 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142361 W10q11_m weight 10 weeks QTL 11 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142362 Tgq27_m triglyceride QTL 27 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4142362 Tgq27_m triglyceride QTL 27 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4142363 Wbcq2_m white blood cell quantitative locus 2 (mouse) qtl MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:16261417 4142363 Wbcq2_m white blood cell quantitative locus 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4142363 Wbcq2_m white blood cell quantitative locus 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4142364 Pbwg18_m postnatal body weight growth 18 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 4142364 Pbwg18_m postnatal body weight growth 18 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16174331 4142365 Egq9_m early growth QTL 9 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142365 Egq9_m early growth QTL 9 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142366 Chlq10_m circulating hormone level QTL 10 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:16782841 4142366 Chlq10_m circulating hormone level QTL 10 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16782841 4142367 Pcts_m plasmacytoma susceptibility (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8105477 4142367 Pcts_m plasmacytoma susceptibility (mouse) qtl MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20111116 MGI PMID:8105477 4142367 Pcts_m plasmacytoma susceptibility (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8105477 4142367 Pcts_m plasmacytoma susceptibility (mouse) qtl MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8105477 4142370 Arrh2_m arrhythmicity 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19173005 4142370 Arrh2_m arrhythmicity 2 (mouse) qtl MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:19173005 4142371 Lacrr1_m light adapted cone retinography response 1 (mouse) qtl MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20111116 MGI PMID:18344449 4142371 Lacrr1_m light adapted cone retinography response 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18344449 4142372 Moo2_m modifier of Odc2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16086382 4142372 Moo2_m modifier of Odc2 (mouse) qtl MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20111116 MGI PMID:16086382 4142372 Moo2_m modifier of Odc2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16086382 4142372 Moo2_m modifier of Odc2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20160506 MGI Created by mouse qtl pipeline PMID:14693723 4142373 Rbcq4_m red blood cell QTL 4 (mouse) qtl MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:16596451 4142373 Rbcq4_m red blood cell QTL 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16596451 4142374 Modor1_m modifier of ocular retardation 1 (mouse) qtl MP:0002697 abnormal eye size IAGP N RGD:5509061 20111116 MGI PMID:16783634 4142374 Modor1_m modifier of ocular retardation 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783634 4142376 Cmn2_m cardiac modifier of nmd 2 (mouse) qtl MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20111116 MGI PMID:16174646 4142376 Cmn2_m cardiac modifier of nmd 2 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16174646 4142376 Cmn2_m cardiac modifier of nmd 2 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16174646 4142377 Secia1_m small effect CIA locus 1 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17244351 4142377 Secia1_m small effect CIA locus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4142377 Secia1_m small effect CIA locus 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4142378 Tcnq5_m Tgfb1 trangenic F2 between C3H and NOD QTL 5 (mouse) qtl MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:18160996 4142378 Tcnq5_m Tgfb1 trangenic F2 between C3H and NOD QTL 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18160996 4142379 Secia3_m small effect CIA locus 3 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17244351 4142379 Secia3_m small effect CIA locus 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4142379 Secia3_m small effect CIA locus 3 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4142380 W3q11_m weight 3 weeks QTL 11 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142380 W3q11_m weight 3 weeks QTL 11 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142381 Mtbcq2_m multiple trait body composition QTL 2 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4142381 Mtbcq2_m multiple trait body composition QTL 2 (mouse) qtl MP:0002981 increased liver weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4142381 Mtbcq2_m multiple trait body composition QTL 2 (mouse) qtl MP:0003397 increased muscle weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4142381 Mtbcq2_m multiple trait body composition QTL 2 (mouse) qtl MP:0004952 increased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4142381 Mtbcq2_m multiple trait body composition QTL 2 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4142381 Mtbcq2_m multiple trait body composition QTL 2 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4142381 Mtbcq2_m multiple trait body composition QTL 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4142381 Mtbcq2_m multiple trait body composition QTL 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4142381 Mtbcq2_m multiple trait body composition QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4142381 Mtbcq2_m multiple trait body composition QTL 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4142381 Mtbcq2_m multiple trait body composition QTL 2 (mouse) qtl MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4142381 Mtbcq2_m multiple trait body composition QTL 2 (mouse) qtl MP:0010024 increased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:17517159 4142383 Vmmt9_m vertebral morphology and mechanical traits 9 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4142383 Vmmt9_m vertebral morphology and mechanical traits 9 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4142384 Hfem3_m Hfe modifier 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15131800 4142384 Hfem3_m Hfe modifier 3 (mouse) qtl MP:0005638 hemochromatosis IAGP N RGD:5509061 20111116 MGI PMID:15131800 4142386 Tgq20_m triglyceride QTL 20 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4142386 Tgq20_m triglyceride QTL 20 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4142387 Bdlnq7_m body length QTL 7 (mouse) qtl MP:0001258 decreased body length IAGP N RGD:5509061 20111116 MGI PMID:17110492 4142387 Bdlnq7_m body length QTL 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4142388 Hfgi2_m Helicobacter felis gastric inflammation 2 (mouse) qtl MP:0001873 stomach inflammation IAGP N RGD:5509061 20111116 MGI PMID:17474149 4142388 Hfgi2_m Helicobacter felis gastric inflammation 2 (mouse) qtl MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20111116 MGI PMID:17474149 4142388 Hfgi2_m Helicobacter felis gastric inflammation 2 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17474149 4142388 Hfgi2_m Helicobacter felis gastric inflammation 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17474149 4142388 Hfgi2_m Helicobacter felis gastric inflammation 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17474149 4142388 Hfgi2_m Helicobacter felis gastric inflammation 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17474149 4142391 Ssrq10_m stress response QTL 10 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17913702 4142391 Ssrq10_m stress response QTL 10 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17913702 4142391 Ssrq10_m stress response QTL 10 (mouse) qtl MP:0010166 increased response to stress-induced hyperthermia IAGP N RGD:5509061 20111116 MGI PMID:17913702 4142392 Psrs6_m psoriasis susceptibility 6 (mouse) qtl MP:0001193 psoriasis IAGP N RGD:5509061 20111116 MGI PMID:16982899 4142392 Psrs6_m psoriasis susceptibility 6 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16982899 4142394 Mssq1_m mandible size and shape QTL 1 (mouse) qtl MP:0004592 small mandible IAGP N RGD:5509061 20111116 MGI PMID:19067046 4142394 Mssq1_m mandible size and shape QTL 1 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142394 Mssq1_m mandible size and shape QTL 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142394 Mssq1_m mandible size and shape QTL 1 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4142395 Lsr1_m listeria resistance (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:6699408 4142395 Lsr1_m listeria resistance (mouse) qtl MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:6699408 4142395 Lsr1_m listeria resistance (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6699408 4142396 Mswtq1_m muscle weight QTL 1 (mouse) qtl MP:0004232 decreased muscle weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4142396 Mswtq1_m muscle weight QTL 1 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4142398 Mskt8_m musculoskeletal traits 8 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:15824847 4142398 Mskt8_m musculoskeletal traits 8 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4142398 Mskt8_m musculoskeletal traits 8 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4142399 Aec1_m autoimmune exocrinopathy 1 (mouse) qtl MP:0000623 decreased salivation IAGP N RGD:5509061 20111116 MGI PMID:12115247 4142399 Aec1_m autoimmune exocrinopathy 1 (mouse) qtl MP:0000623 decreased salivation IAGP N RGD:5509061 20111116 MGI PMID:12614028 4142399 Aec1_m autoimmune exocrinopathy 1 (mouse) qtl MP:0000623 decreased salivation IAGP N RGD:5509061 20111116 MGI PMID:16918699 4142399 Aec1_m autoimmune exocrinopathy 1 (mouse) qtl MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20111116 MGI PMID:16918699 4142399 Aec1_m autoimmune exocrinopathy 1 (mouse) qtl MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20111116 MGI PMID:16918699 4142399 Aec1_m autoimmune exocrinopathy 1 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20111116 MGI PMID:12115247 4142399 Aec1_m autoimmune exocrinopathy 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115247 4142399 Aec1_m autoimmune exocrinopathy 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115247 4142399 Aec1_m autoimmune exocrinopathy 1 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115247 4142399 Aec1_m autoimmune exocrinopathy 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115247 4142399 Aec1_m autoimmune exocrinopathy 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12115247 4142399 Aec1_m autoimmune exocrinopathy 1 (mouse) qtl MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20111116 MGI PMID:12115247 4142399 Aec1_m autoimmune exocrinopathy 1 (mouse) qtl MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141211 MGI PMID:16918699 4142400 Tgq24_m triglyceride QTL 24 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4142400 Tgq24_m triglyceride QTL 24 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4142401 Egq10_m early growth QTL 10 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142401 Egq10_m early growth QTL 10 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142402 Ccs1_m colon cancer susceptibility 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7806225 4142402 Ccs1_m colon cancer susceptibility 1 (mouse) qtl MP:0002020 increased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:7806225 4142402 Ccs1_m colon cancer susceptibility 1 (mouse) qtl MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:7806225 4142403 Hrwq_m heart weight QTL (mouse) qtl MP:0002834 decreased heart weight IAGP N RGD:5509061 20111116 MGI PMID:18239664 4142403 Hrwq_m heart weight QTL (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18239664 4142404 Lpn1_m NZ lupus nephritis 1 (mouse) qtl MP:0001859 kidney inflammation IAGP N RGD:5509061 20111116 MGI PMID:681876 4142404 Lpn1_m NZ lupus nephritis 1 (mouse) qtl MP:0002962 increased urine protein level IAGP N RGD:5509061 20111116 MGI PMID:681876 4142404 Lpn1_m NZ lupus nephritis 1 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:681876 4142404 Lpn1_m NZ lupus nephritis 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:681876 4142404 Lpn1_m NZ lupus nephritis 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:681876 4142407 Blacv1_m basolateral amygdala complex volume 1 (mouse) qtl MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20111116 MGI PMID:17131200 4142407 Blacv1_m basolateral amygdala complex volume 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17131200 4142409 Ads4_m anti dsDNA antibody 4 (mouse) qtl MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20111116 MGI PMID:6864161 4142409 Ads4_m anti dsDNA antibody 4 (mouse) qtl MP:0002962 increased urine protein level IAGP N RGD:5509061 20111116 MGI PMID:1826267 4142409 Ads4_m anti dsDNA antibody 4 (mouse) qtl MP:0004798 decreased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:1826267 4142409 Ads4_m anti dsDNA antibody 4 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20111116 MGI PMID:6864161 4142409 Ads4_m anti dsDNA antibody 4 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6864161 4142409 Ads4_m anti dsDNA antibody 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6864161 4142409 Ads4_m anti dsDNA antibody 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6864161 4142409 Ads4_m anti dsDNA antibody 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:6864161 4142410 Mssq4_m mandible size and shape QTL 4 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142410 Mssq4_m mandible size and shape QTL 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142410 Mssq4_m mandible size and shape QTL 4 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4142411 Spw4_m spleen weight 4 (mouse) qtl MP:0004953 decreased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:18552208 4142411 Spw4_m spleen weight 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4142411 Spw4_m spleen weight 4 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18552208 4142413 Ath30_m atherosclerosis 30 (mouse) qtl MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20111116 MGI PMID:17641228 4142413 Ath30_m atherosclerosis 30 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17641228 4142414 Pregq4_m pregnancy QTL 4 (mouse) qtl MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20111116 MGI PMID:16547111 4142414 Pregq4_m pregnancy QTL 4 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16547111 4142415 Mchq1_m mean corpuscular hemoglobin QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16596451 4142415 Mchq1_m mean corpuscular hemoglobin QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20171215 MGI Created by mouse qtl pipeline PMID:24967628|PMID:16596451 4142415 Mchq1_m mean corpuscular hemoglobin QTL 1 (mouse) qtl MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20111116 MGI PMID:16596451 4142416 Egq11_m early growth QTL 11 (mouse) qtl MP:0002865 increased growth rate IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142416 Egq11_m early growth QTL 11 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142418 Ssnt2_m short snout 2 (mouse) qtl MP:0000445 short snout IAGP N RGD:5509061 20111116 MGI PMID:14530301 4142418 Ssnt2_m short snout 2 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20140627 MGI Created by mouse qtl pipeline PMID:14530301 4142418 Ssnt2_m short snout 2 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:14530301 4142419 Tgq26_m triglyceride QTL 26 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4142419 Tgq26_m triglyceride QTL 26 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4142420 Foc1_m follicular center cell lymphoma 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8275476 4142420 Foc1_m follicular center cell lymphoma 1 (mouse) qtl MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8275476 4142422 Albq5_m albuminuria QTL 5 (mouse) qtl MP:0002871 albuminuria IAGP N RGD:5509061 20111116 MGI PMID:17804484 4142422 Albq5_m albuminuria QTL 5 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17804484 4142422 Albq5_m albuminuria QTL 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17804484 4142424 Swqnd2_m spleen weight QTL 2 (mouse) qtl MP:0004953 decreased spleen weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4142424 Swqnd2_m spleen weight QTL 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4142424 Swqnd2_m spleen weight QTL 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4142425 Hdlq52_m HDL QTL 52 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18772481 4142425 Hdlq52_m HDL QTL 52 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18772481 4142426 Mlca2_m modifier of locomotor activity 2 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16436185 4142426 Mlca2_m modifier of locomotor activity 2 (mouse) qtl MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:16436185 4142427 Hdlq35_m HDL QTL 35 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16685081 4142427 Hdlq35_m HDL QTL 35 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16685081 4142428 Modvl1_m modifier of vacuolated lens 1 (mouse) qtl MP:0003054 spina bifida IAGP N RGD:5509061 20111116 MGI PMID:18250320 4142428 Modvl1_m modifier of vacuolated lens 1 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18250320 4142428 Modvl1_m modifier of vacuolated lens 1 (mouse) qtl MP:0005380 embryo phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18250320 4142431 Mpdk3_m modifier of polycystic kidney disease 3 (mouse) qtl MP:0002706 abnormal kidney size IAGP N RGD:5509061 20111116 MGI PMID:15728779 4142431 Mpdk3_m modifier of polycystic kidney disease 3 (mouse) qtl MP:0003917 increased kidney weight IAGP N RGD:5509061 20111116 MGI PMID:15728779 4142431 Mpdk3_m modifier of polycystic kidney disease 3 (mouse) qtl MP:0005367 renal/urinary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15728779 4142431 Mpdk3_m modifier of polycystic kidney disease 3 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:15728779 4142432 Msmr1_m MSM lymphoma resistance 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8706013 4142432 Msmr1_m MSM lymphoma resistance 1 (mouse) qtl MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8706013 4142432 Msmr1_m MSM lymphoma resistance 1 (mouse) qtl MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20111116 MGI PMID:8706013 4142432 Msmr1_m MSM lymphoma resistance 1 (mouse) qtl MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20131227 MGI PMID:8706013 4142433 Hbnr1_m Heligmosomoides bakeri nematode resistance 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:12647241 4142434 Fcs4_m fibroblast cell senescence 4 (mouse) qtl MP:0000351 increased cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:16842493 4142434 Fcs4_m fibroblast cell senescence 4 (mouse) qtl MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:16842493 4142434 Fcs4_m fibroblast cell senescence 4 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16842493 4142438 Agp2_m anti gp70 immune complex 2 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6217253 4142438 Agp2_m anti gp70 immune complex 2 (mouse) qtl MP:0005615 increased susceptibility to type III hypersensitivity reaction IAGP N RGD:5509061 20111116 MGI PMID:6217253 4142442 Modm_m modifier of methylation (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:11230162 4142442 Modm_m modifier of methylation (mouse) qtl MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20111116 MGI PMID:11230162 4142443 Pgis1_m proteoglycan induced spondylitis 1 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:16081819 4142443 Pgis1_m proteoglycan induced spondylitis 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16081819 4142443 Pgis1_m proteoglycan induced spondylitis 1 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16081819 4142447 Pbwg1.7_m postnatal body weight growth 1.7 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17514348 4142447 Pbwg1.7_m postnatal body weight growth 1.7 (mouse) qtl MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:17514348 4142448 Tailq6_m tail length QTL 6 (mouse) qtl MP:0002758 long tail IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142448 Tailq6_m tail length QTL 6 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142449 Tgq14_m triglyceride QTL 14 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4142449 Tgq14_m triglyceride QTL 14 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4142450 Lmr16_m leishmaniasis resistance 16 (mouse) qtl MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20111116 MGI PMID:16511555 4142450 Lmr16_m leishmaniasis resistance 16 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16511555 4142450 Lmr16_m leishmaniasis resistance 16 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16511555 4142450 Lmr16_m leishmaniasis resistance 16 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16511555 4142453 Adip11_m adiposity 11 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16416088 4142453 Adip11_m adiposity 11 (mouse) qtl MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4142453 Adip11_m adiposity 11 (mouse) qtl MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20111116 MGI PMID:16416088 4142455 Elnv_m epilepsy naive (mouse) qtl MP:0002064 seizures IAGP N RGD:5509061 20111116 MGI PMID:17010098 4142455 Elnv_m epilepsy naive (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17010098 4142455 Elnv_m epilepsy naive (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17010098 4142456 Hdlq55_m HDL QTL 55 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18772481 4142456 Hdlq55_m HDL QTL 55 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18772481 4142457 Hmtb3_m hemostasis and thrombosis 3 (mouse) qtl MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20111116 MGI PMID:17022820 4142457 Hmtb3_m hemostasis and thrombosis 3 (mouse) qtl MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20111116 MGI PMID:17022820 4142457 Hmtb3_m hemostasis and thrombosis 3 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17022820 4142457 Hmtb3_m hemostasis and thrombosis 3 (mouse) qtl MP:0005607 decreased bleeding time IAGP N RGD:5509061 20111116 MGI PMID:17022820 4142458 Spmd2_m spermatogenesis defect 2 (mouse) qtl MP:0002687 oligozoospermia IAGP N RGD:5509061 20111116 MGI PMID:16651692 4142458 Spmd2_m spermatogenesis defect 2 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:16651692 4142458 Spmd2_m spermatogenesis defect 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16651692 4142460 Nilac10_m nicotine induced locomotor activity 10 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16176386 4142460 Nilac10_m nicotine induced locomotor activity 10 (mouse) qtl MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:16176386 4142460 Nilac10_m nicotine induced locomotor activity 10 (mouse) qtl MP:0009752 enhanced behavioral response to nicotine IAGP N RGD:5509061 20111116 MGI PMID:19083055 4142462 Rtwq2_m reduced testis weight QTL 2 (mouse) qtl MP:0004852 decreased testis weight IAGP N RGD:5509061 20111116 MGI PMID:18689897 4142462 Rtwq2_m reduced testis weight QTL 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18689897 4142462 Rtwq2_m reduced testis weight QTL 2 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18689897 4142463 Mmom2_m mammary modifier of Min 2 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18056448 4142463 Mmom2_m mammary modifier of Min 2 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18056448 4142463 Mmom2_m mammary modifier of Min 2 (mouse) qtl MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20111116 MGI PMID:18056448 4142463 Mmom2_m mammary modifier of Min 2 (mouse) qtl MP:0010771 integument phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18056448 4142465 Pbwg17_m postnatal body weight growth 17 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:16174331 4142465 Pbwg17_m postnatal body weight growth 17 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16174331 4142467 Wbcq1_m white blood cell quantitative locus 1 (mouse) qtl MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20111116 MGI PMID:16261417 4142467 Wbcq1_m white blood cell quantitative locus 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4142467 Wbcq1_m white blood cell quantitative locus 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4142468 Hdlq56_m HDL QTL 56 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:18772481 4142468 Hdlq56_m HDL QTL 56 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18772481 4142469 Mpvq2_m mean platelet volume locus 2 (mouse) qtl MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20111116 MGI PMID:16261417 4142469 Mpvq2_m mean platelet volume locus 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16261417 4142470 Drinksac4_m drink saccharin 4 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4142470 Drinksac4_m drink saccharin 4 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4142471 Fcs1_m fibroblast cell senescence 1 (mouse) qtl MP:0000351 increased cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:16842493 4142471 Fcs1_m fibroblast cell senescence 1 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16842493 4142472 Mssq17_m mandible size and shape QTL 17 (mouse) qtl MP:0005382 craniofacial phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142472 Mssq17_m mandible size and shape QTL 17 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19067046 4142472 Mssq17_m mandible size and shape QTL 17 (mouse) qtl MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 4142473 Chlq11_m circulating hormone level QTL 11 (mouse) qtl MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:16782841 4142473 Chlq11_m circulating hormone level QTL 11 (mouse) qtl MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20111116 MGI PMID:16782841 4142473 Chlq11_m circulating hormone level QTL 11 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16782841 4142474 Lskpf2_m LSK cell population frequency 2 (mouse) qtl MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20111116 MGI PMID:18288524 4142474 Lskpf2_m LSK cell population frequency 2 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18288524 4142475 Ity2a_m immunity to S. typhimurium 2a (mouse) qtl MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20111116 MGI PMID:17660555 4142475 Ity2a_m immunity to S. typhimurium 2a (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17660555 4142476 Rrsv_m resistance to Rous sarcoma (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:209108 4142476 Rrsv_m resistance to Rous sarcoma (mouse) qtl MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20111116 MGI PMID:209108 4142476 Rrsv_m resistance to Rous sarcoma (mouse) qtl MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20111116 MGI PMID:209108 4142476 Rrsv_m resistance to Rous sarcoma (mouse) qtl MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20111116 MGI PMID:209108 4142477 Wg2a_m weight gain in high growth mice 2a (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:17694346 4142477 Wg2a_m weight gain in high growth mice 2a (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17694346 4142479 Secia4_m small effect CIA locus 4 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20111116 MGI PMID:17244351 4142479 Secia4_m small effect CIA locus 4 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4142479 Secia4_m small effect CIA locus 4 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17244351 4142481 Gct1_m granulosa cell tumorigenesis 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15735010|PMID:9721880 4142481 Gct1_m granulosa cell tumorigenesis 1 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20150529 MGI Created by mouse qtl pipeline PMID:9721880 4142481 Gct1_m granulosa cell tumorigenesis 1 (mouse) qtl MP:0005379 endocrine/exocrine gland phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9721880 4142481 Gct1_m granulosa cell tumorigenesis 1 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:9721880 4142482 Abshq4_m abnormal sperm head QTL 4 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:18689897 4142482 Abshq4_m abnormal sperm head QTL 4 (mouse) qtl MP:0005389 reproductive system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18689897 4142482 Abshq4_m abnormal sperm head QTL 4 (mouse) qtl MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20111116 MGI PMID:18689897 4142483 Mtbcq5_m multiple trait body composition QTL 5 (mouse) qtl MP:0001262 decreased body weight IAGP N RGD:5509061 20111116 MGI PMID:17517159 4142483 Mtbcq5_m multiple trait body composition QTL 5 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17517159 4142484 Vmmt8_m vertebral morphology and mechanical traits 8 (mouse) qtl MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20111116 MGI PMID:17049325 4142484 Vmmt8_m vertebral morphology and mechanical traits 8 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17049325 4142485 Modor2_m modifier of ocular retardation 2 (mouse) qtl MP:0002697 abnormal eye size IAGP N RGD:5509061 20111116 MGI PMID:16783634 4142485 Modor2_m modifier of ocular retardation 2 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16783634 4142486 Cmn1_m cardiac modifier of nmd 1 (mouse) qtl MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20111116 MGI PMID:16174646 4142486 Cmn1_m cardiac modifier of nmd 1 (mouse) qtl MP:0005369 muscle phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16174646 4142486 Cmn1_m cardiac modifier of nmd 1 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16174646 4142487 Bmd37_m bone mineral density 37 (mouse) qtl MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20111116 MGI PMID:17179051 4142487 Bmd37_m bone mineral density 37 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17179051 4142489 Ath25_m atherosclerosis 25 (mouse) qtl MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20111116 MGI PMID:16373612 4142489 Ath25_m atherosclerosis 25 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16373612 4142491 Cinda5_m cytokine induced activation 5 (mouse) qtl MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20111116 MGI PMID:15551356 4142491 Cinda5_m cytokine induced activation 5 (mouse) qtl MP:0005384 cellular phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15551356 4142491 Cinda5_m cytokine induced activation 5 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15551356 4142491 Cinda5_m cytokine induced activation 5 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15551356 4142492 Hfem2_m Hfe modifier 2 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15131800 4142492 Hfem2_m Hfe modifier 2 (mouse) qtl MP:0005638 hemochromatosis IAGP N RGD:5509061 20111116 MGI PMID:15131800 4142495 Hdlq45_m HDL QTL 45 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16951076 4142495 Hdlq45_m HDL QTL 45 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16951076 4142496 W6q8_m weight 6 weeks QTL 8 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15058380 4142496 W6q8_m weight 6 weeks QTL 8 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15058380 4142497 Fatmq1_m total fat pad mass QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:17110492 4142497 Fatmq1_m total fat pad mass QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:17110492 4142497 Fatmq1_m total fat pad mass QTL 1 (mouse) qtl MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20111116 MGI PMID:17110492 4142498 Hctq1_m hematocrit QTL 1 (mouse) qtl MP:0002608 increased hematocrit IAGP N RGD:5509061 20111116 MGI PMID:16596451 4142498 Hctq1_m hematocrit QTL 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16596451 4142499 Mskt7_m musculoskeletal traits 7 (mouse) qtl MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20111116 MGI PMID:15824847 4142499 Mskt7_m musculoskeletal traits 7 (mouse) qtl MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20111116 MGI PMID:15824847 4142499 Mskt7_m musculoskeletal traits 7 (mouse) qtl MP:0001257 increased body length IAGP N RGD:5509061 20111116 MGI PMID:15824847 4142499 Mskt7_m musculoskeletal traits 7 (mouse) qtl MP:0001260 increased body weight IAGP N RGD:5509061 20111116 MGI PMID:15824847 4142499 Mskt7_m musculoskeletal traits 7 (mouse) qtl MP:0005371 limbs/digits/tail phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4142499 Mskt7_m musculoskeletal traits 7 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4142499 Mskt7_m musculoskeletal traits 7 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15824847 4142499 Mskt7_m musculoskeletal traits 7 (mouse) qtl MP:0006087 increased body mass index IAGP N RGD:5509061 20111116 MGI PMID:15824847 4142500 Morq1_m modifier of Rs1 QTL 1 (mouse) qtl MP:0005391 vision/eye phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18245825 4142500 Morq1_m modifier of Rs1 QTL 1 (mouse) qtl MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20111116 MGI PMID:18245825 4142501 Drinkkcl5_m drink potassium chloride 5 (mouse) qtl MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20111116 MGI PMID:18363849 4142501 Drinkkcl5_m drink potassium chloride 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18363849 4142502 Ads3_m anti dsDNA antibody 3 (mouse) qtl MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20111116 MGI PMID:6864161 4142502 Ads3_m anti dsDNA antibody 3 (mouse) qtl MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20111116 MGI PMID:6642573 4142502 Ads3_m anti dsDNA antibody 3 (mouse) qtl MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20111116 MGI PMID:6864161 4142502 Ads3_m anti dsDNA antibody 3 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6864161 4142502 Ads3_m anti dsDNA antibody 3 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:6864161 4142503 Chldq4_m cholesterol and HDL QTL 4 (mouse) qtl MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16254318 4142503 Chldq4_m cholesterol and HDL QTL 4 (mouse) qtl MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:16254318 4142503 Chldq4_m cholesterol and HDL QTL 4 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:16254318 4142505 Crl1_m complement receptor lymphocyte 1 (mouse) qtl MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20111116 MGI PMID:4545163 4142505 Crl1_m complement receptor lymphocyte 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:4545163 4142505 Crl1_m complement receptor lymphocyte 1 (mouse) qtl MP:0005397 hematopoietic system phenotype IEA N RGD:704405 20131213 MGI Created by mouse qtl pipeline PMID:4545163 4142506 Imm1_m IgM serum level modifier 1 (mouse) qtl MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20111116 MGI PMID:6334582 4142506 Imm1_m IgM serum level modifier 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:6334582 4142507 Obrq13_m obesity resistance QTL 13 (mouse) qtl MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20111116 MGI PMID:19137372 4142507 Obrq13_m obesity resistance QTL 13 (mouse) qtl MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:19137372 4142507 Obrq13_m obesity resistance QTL 13 (mouse) qtl MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20111116 MGI PMID:19137372 4142507 Obrq13_m obesity resistance QTL 13 (mouse) qtl MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20111116 MGI PMID:19137372 4142507 Obrq13_m obesity resistance QTL 13 (mouse) qtl MP:0005331 insulin resistance IAGP N RGD:5509061 20111116 MGI PMID:19137372 4142507 Obrq13_m obesity resistance QTL 13 (mouse) qtl MP:0005370 liver/biliary system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19137372 4142507 Obrq13_m obesity resistance QTL 13 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19137372 4142507 Obrq13_m obesity resistance QTL 13 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:19137372 4142507 Obrq13_m obesity resistance QTL 13 (mouse) qtl MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20111116 MGI PMID:19137372 4142507 Obrq13_m obesity resistance QTL 13 (mouse) qtl MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20111116 MGI PMID:19137372 4142508 Tgq25_m triglyceride QTL 25 (mouse) qtl MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20111116 MGI PMID:18503028 4142508 Tgq25_m triglyceride QTL 25 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:18503028 4143210 Sox10m5_m Sox10Dom modifier 5 (mouse) qtl MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20150618 MGI PMID:15843399 4143210 Sox10m5_m Sox10Dom modifier 5 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:15843399 4890782 Actc1dt actin, alpha, cardiac muscle 1 divergent transcript gene MP:0002833 increased heart weight IAGP N RGD:5509061 20240606 MGI PMID:30832495 4890782 Actc1dt actin, alpha, cardiac muscle 1 divergent transcript gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20240606 MGI PMID:30832495 4890782 Actc1dt actin, alpha, cardiac muscle 1 divergent transcript gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20240606 MGI PMID:30832495 4890782 Actc1dt actin, alpha, cardiac muscle 1 divergent transcript gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20240606 MGI PMID:30832495 4890782 Actc1dt actin, alpha, cardiac muscle 1 divergent transcript gene MP:0006321 increased myocardial fiber number IAGP N RGD:5509061 20240606 MGI PMID:30832495 4890782 Actc1dt actin, alpha, cardiac muscle 1 divergent transcript gene MP:0031216 decreased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20240606 MGI PMID:30832495 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0001127 small ovary IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0001147 small testis IAGP N RGD:5509061 20211223 MGI PMID:34820371 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0001147 small testis IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0001925 male infertility IAGP N RGD:5509061 20211223 MGI PMID:34820371 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0001925 male infertility IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0001925 male infertility IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20211223 MGI PMID:34820371 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20211223 MGI PMID:34820371 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20211223 MGI PMID:34820371 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0005159 azoospermia IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20211223 MGI PMID:34820371 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20211223 MGI PMID:34820371 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0008967 absent chiasmata formation IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0008967 absent chiasmata formation IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20211223 MGI PMID:34820371 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20211223 MGI PMID:34820371 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20211223 MGI PMID:34820371 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20230420 MGI PMID:31000436 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20211223 MGI PMID:34820371 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20240808 MGI PMID:31003867 5134233 Ankrd31 ankyrin repeat domain 31 gene MP:0031474 increased female germ cell apoptosis IAGP N RGD:5509061 20240808 MGI PMID:31000436 5134290 Mir378b microRNA 378b gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20210805 MGI PMID:34067003 5134290 Mir378b microRNA 378b gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20210805 MGI PMID:34067003 5134290 Mir378b microRNA 378b gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20210805 MGI PMID:34067003 5134290 Mir378b microRNA 378b gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20210805 MGI PMID:34067003 5134290 Mir378b microRNA 378b gene MP:0020186 abnormal susceptibility to bacterial infection IAGP N RGD:5509061 20210805 MGI PMID:34067003 5134290 Mir378b microRNA 378b gene MP:0031424 enhanced female fertility IAGP N RGD:5509061 20220714 MGI PMID:34067003 5137760 Tincr TINCR ubiquitin domain containing gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 5137760 Tincr TINCR ubiquitin domain containing gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 5137760 Tincr TINCR ubiquitin domain containing gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 5137760 Tincr TINCR ubiquitin domain containing gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20231130 MGI PMID:34351912 5137760 Tincr TINCR ubiquitin domain containing gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 5137760 Tincr TINCR ubiquitin domain containing gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20231130 MGI PMID:34351912 5137760 Tincr TINCR ubiquitin domain containing gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20230601 MGI 5137760 Tincr TINCR ubiquitin domain containing gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20231130 MGI PMID:34351912 5143795 Cd200l2 CD200 molecule like 2 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20220922 MGI PMID:34921782 5143795 Cd200l2 CD200 molecule like 2 gene MP:0020954 decreased mechanical nociceptive threshold IAGP N RGD:5509061 20220922 MGI PMID:34921782 5144854 Tarbp1 TAR RNA binding protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 5144854 Tarbp1 TAR RNA binding protein 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0002083 premature death IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0012188 increased regulatory T cell apoptosis IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145117 Altre aging liver Treg-expressed non-protein coding RNA gene MP:0031269 increased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20231214 MGI PMID:37277640 5145538 Gm16364 predicted gene 16364 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20221201 MGI PMID:34750570 5145538 Gm16364 predicted gene 16364 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20221201 MGI PMID:34750570 5145538 Gm16364 predicted gene 16364 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20221201 MGI PMID:34750570 5145538 Gm16364 predicted gene 16364 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20221201 MGI PMID:34750570 5145538 Gm16364 predicted gene 16364 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20221201 MGI PMID:34750570 5145538 Gm16364 predicted gene 16364 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20221201 MGI PMID:34750570 5145538 Gm16364 predicted gene 16364 gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20221201 MGI PMID:34750570 5145538 Gm16364 predicted gene 16364 gene MP:0020868 decreased lipogenesis IAGP N RGD:5509061 20221201 MGI PMID:34750570 5145538 Gm16364 predicted gene 16364 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20221201 MGI PMID:34750570 5145762 Trp53cor1 tumor protein p53 pathway corepressor 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:24381249 5145795 Mptx2 mucosal pentraxin 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20220804 MGI PMID:35609377 5145894 Gm16685 predicted gene, 16685 gene MP:0013299 decreased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20210429 MGI PMID:33239342 5146005 Gm17266 predicted gene, 17266 gene MP:0001147 small testis IAGP N RGD:5509061 20240613 MGI PMID:38697008 5146058 Hotair HOX transcript antisense RNA (non-protein coding) gene MP:0000553 absent radius IAGP N RGD:5509061 20160915 MGI PMID:24075995 5146058 Hotair HOX transcript antisense RNA (non-protein coding) gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20160915 MGI PMID:24075995 5146058 Hotair HOX transcript antisense RNA (non-protein coding) gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20161229 MGI PMID:25909911 5146058 Hotair HOX transcript antisense RNA (non-protein coding) gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20161229 MGI PMID:25909911 5146058 Hotair HOX transcript antisense RNA (non-protein coding) gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20160915 MGI PMID:24075995 5146058 Hotair HOX transcript antisense RNA (non-protein coding) gene MP:0004614 caudal vertebral transformation IAGP N RGD:5509061 20160915 MGI PMID:24075995 5146058 Hotair HOX transcript antisense RNA (non-protein coding) gene MP:0004614 caudal vertebral transformation IAGP N RGD:5509061 20161229 MGI PMID:25909911 5146058 Hotair HOX transcript antisense RNA (non-protein coding) gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20160915 MGI PMID:24075995 5146058 Hotair HOX transcript antisense RNA (non-protein coding) gene MP:0004639 fused metacarpal bones IAGP N RGD:5509061 20160915 MGI PMID:24075995 5146058 Hotair HOX transcript antisense RNA (non-protein coding) gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20160915 MGI PMID:24075995 5146058 Hotair HOX transcript antisense RNA (non-protein coding) gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20160915 MGI PMID:24075995 5146065 Zfp683 zinc finger protein 683 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:22885984 5146065 Zfp683 zinc finger protein 683 gene MP:0008036 abnormal NK T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22885984 5146065 Zfp683 zinc finger protein 683 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:22885984 5146065 Zfp683 zinc finger protein 683 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22885984 5147262 Spmip2 sperm associated microtubule inner protein 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20231207 MGI 5147262 Spmip2 sperm associated microtubule inner protein 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 5490551 Irm1_m inflammatory response modulator 1 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:20610646 5491191 Mobq2_m multigenic obesity QTL 2 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:8349816|PMID:7706460 5491192 Mobq1_m multigenic obesity QTL 1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7706460|PMID:8349816 5491192 Mobq1_m multigenic obesity QTL 1 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7706460|PMID:8349816 5491192 Mobq1_m multigenic obesity QTL 1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7706460|PMID:8349816 5491192 Mobq1_m multigenic obesity QTL 1 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7706460|PMID:8349816 5491193 Mobq4_m multigenic obesity QTL 4 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7706460 5491194 Mobq3_m multigenic obesity QTL 3 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:7706460 5491195 Mobq8_m multigenic obesity QTL 8 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9616220 5491196 Mobq6_m multigenic obesity QTL 6 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9616220 5491196 Mobq6_m multigenic obesity QTL 6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9616220 5491196 Mobq6_m multigenic obesity QTL 6 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9616220 5491196 Mobq6_m multigenic obesity QTL 6 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9616220 5491196 Mobq6_m multigenic obesity QTL 6 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9616220 5491197 Mobq5_m multigenic obesity QTL 5 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9616220 5491197 Mobq5_m multigenic obesity QTL 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9616220 5491197 Mobq5_m multigenic obesity QTL 5 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9616220 5491198 Mobq7_m multigenic obesity QTL 7 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120116 MGI Created by mouse qtl pipeline PMID:9616220 5509679 Dcdc2b doublecortin domain containing 2b gene MP:0002608 increased hematocrit IEA N RGD:5509061 20201022 MGI 5509679 Dcdc2b doublecortin domain containing 2b gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 5684527 Duxf2 double homeobox family member 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20231026 MGI PMID:31591446 5685421 A930024E05Rik RIKEN cDNA A930024E05 gene gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20220721 MGI PMID:28319097 5685421 A930024E05Rik RIKEN cDNA A930024E05 gene gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20220721 MGI PMID:28319097 5685421 A930024E05Rik RIKEN cDNA A930024E05 gene gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20220721 MGI PMID:28319097 5685421 A930024E05Rik RIKEN cDNA A930024E05 gene gene MP:0013893 decreased common lymphocyte progenitor cell number IAGP N RGD:5509061 20220721 MGI PMID:28319097 5685448 4930591A17Rik RIKEN cDNA 4930591A17 gene gene MP:0003960 increased lean body mass IEA N RGD:5509061 20141003 MGI 5685448 4930591A17Rik RIKEN cDNA 4930591A17 gene gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 5685448 4930591A17Rik RIKEN cDNA 4930591A17 gene gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20150108 MGI 5685448 4930591A17Rik RIKEN cDNA 4930591A17 gene gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 5685724 D930028M14Rik RIKEN cDNA D930028M14 gene gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 5685724 D930028M14Rik RIKEN cDNA D930028M14 gene gene MP:0010602 abnormal pulmonary valve cusp morphology IEA N RGD:5509061 20170504 MGI 5685724 D930028M14Rik RIKEN cDNA D930028M14 gene gene MP:0010912 herniated liver IEA N RGD:5509061 20170504 MGI 5685724 D930028M14Rik RIKEN cDNA D930028M14 gene gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 5685724 D930028M14Rik RIKEN cDNA D930028M14 gene gene MP:0012303 umbilical vein stenosis IEA N RGD:5509061 20170504 MGI 5685724 D930028M14Rik RIKEN cDNA D930028M14 gene gene MP:0013826 absent hypoglossal canal IEA N RGD:5509061 20170504 MGI 5685724 D930028M14Rik RIKEN cDNA D930028M14 gene gene MP:0013831 vagus nerve compression IEA N RGD:5509061 20170504 MGI 5685724 D930028M14Rik RIKEN cDNA D930028M14 gene gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20170504 MGI 5685724 D930028M14Rik RIKEN cDNA D930028M14 gene gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 5685724 D930028M14Rik RIKEN cDNA D930028M14 gene gene MP:0013847 retropleural edema IEA N RGD:5509061 20170504 MGI 5685724 D930028M14Rik RIKEN cDNA D930028M14 gene gene MP:0013849 absent abducens nerve IEA N RGD:5509061 20170504 MGI 5685724 D930028M14Rik RIKEN cDNA D930028M14 gene gene MP:0013915 abnormal brachial plexus formation IEA N RGD:5509061 20170504 MGI 5685853 Silc1 sciatic injury induced lincRNA upregulator of SOX11 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20210401 MGI PMID:30401432 5685853 Silc1 sciatic injury induced lincRNA upregulator of SOX11 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20210401 MGI PMID:30401432 5686458 Fsbp fibrinogen silencer binding protein gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20230720 MGI 619553 Crebbp CREB binding protein gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9294190 619553 Crebbp CREB binding protein gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20141003 MGI PMID:9294190 619553 Crebbp CREB binding protein gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0000091 short premaxilla IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9294190 619553 Crebbp CREB binding protein gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9294190 619553 Crebbp CREB binding protein gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9294190 619553 Crebbp CREB binding protein gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:9294190 619553 Crebbp CREB binding protein gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:10673499 619553 Crebbp CREB binding protein gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10673499 619553 Crebbp CREB binding protein gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0000263 absent organized vascular network IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0000264 failure of vascular branching IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:14517255 619553 Crebbp CREB binding protein gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22198154 619553 Crebbp CREB binding protein gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:22198154 619553 Crebbp CREB binding protein gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:10673499 619553 Crebbp CREB binding protein gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:16237459 619553 Crebbp CREB binding protein gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0000447 flattened snout IAGP N RGD:5509061 20171019 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0000449 broad nasal bridge IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10673499 619553 Crebbp CREB binding protein gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22198154 619553 Crebbp CREB binding protein gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:16428436 619553 Crebbp CREB binding protein gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:12384703 619553 Crebbp CREB binding protein gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16428436 619553 Crebbp CREB binding protein gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9590171 619553 Crebbp CREB binding protein gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10673499 619553 Crebbp CREB binding protein gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:9590171 619553 Crebbp CREB binding protein gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22198154 619553 Crebbp CREB binding protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12384703 619553 Crebbp CREB binding protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15452871 619553 Crebbp CREB binding protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16237459 619553 Crebbp CREB binding protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20160519 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160519 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20160519 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160519 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20160519 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20160519 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20160519 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9590171 619553 Crebbp CREB binding protein gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10673499 619553 Crebbp CREB binding protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16237459 619553 Crebbp CREB binding protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9294190 619553 Crebbp CREB binding protein gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:22198154 619553 Crebbp CREB binding protein gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16237459 619553 Crebbp CREB binding protein gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14998493 619553 Crebbp CREB binding protein gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16428436 619553 Crebbp CREB binding protein gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:10673499 619553 Crebbp CREB binding protein gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15146178 619553 Crebbp CREB binding protein gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15146178 619553 Crebbp CREB binding protein gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15452871 619553 Crebbp CREB binding protein gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:14517255 619553 Crebbp CREB binding protein gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15452871 619553 Crebbp CREB binding protein gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:9294190 619553 Crebbp CREB binding protein gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10673499 619553 Crebbp CREB binding protein gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22198154 619553 Crebbp CREB binding protein gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14998493 619553 Crebbp CREB binding protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15452871 619553 Crebbp CREB binding protein gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:16237459 619553 Crebbp CREB binding protein gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:16237459 619553 Crebbp CREB binding protein gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22198154 619553 Crebbp CREB binding protein gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22198154 619553 Crebbp CREB binding protein gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20160519 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:15146178 619553 Crebbp CREB binding protein gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0002923 increased post-tetanic potentiation IAGP N RGD:5509061 20160519 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9294190 619553 Crebbp CREB binding protein gene MP:0003542 abnormal vascular endothelial cell development IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:15452871 619553 Crebbp CREB binding protein gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:16237459 619553 Crebbp CREB binding protein gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20160519 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20160519 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0004379 wide frontal bone IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0004471 short nasal bone IAGP N RGD:5509061 20160519 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20160519 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0004679 xiphoid process foramen IAGP N RGD:5509061 20141003 MGI PMID:9294190 619553 Crebbp CREB binding protein gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22198154 619553 Crebbp CREB binding protein gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:21289174 619553 Crebbp CREB binding protein gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22198154 619553 Crebbp CREB binding protein gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10673499 619553 Crebbp CREB binding protein gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16428436 619553 Crebbp CREB binding protein gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16428436 619553 Crebbp CREB binding protein gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16428436 619553 Crebbp CREB binding protein gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14998493 619553 Crebbp CREB binding protein gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16428436 619553 Crebbp CREB binding protein gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15146178 619553 Crebbp CREB binding protein gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20160519 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15146178 619553 Crebbp CREB binding protein gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15146178 619553 Crebbp CREB binding protein gene MP:0005385 cardiovascular system phenotype IAGP N RGD:5509061 20211216 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0005385 cardiovascular system phenotype IAGP N RGD:5509061 20211216 MGI PMID:9294190 619553 Crebbp CREB binding protein gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15146178 619553 Crebbp CREB binding protein gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0006057 decreased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:16237459 619553 Crebbp CREB binding protein gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:16428436 619553 Crebbp CREB binding protein gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22198154 619553 Crebbp CREB binding protein gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16428436 619553 Crebbp CREB binding protein gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14998493 619553 Crebbp CREB binding protein gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22198154 619553 Crebbp CREB binding protein gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22198154 619553 Crebbp CREB binding protein gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:10673499 619553 Crebbp CREB binding protein gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22198154 619553 Crebbp CREB binding protein gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10673499 619553 Crebbp CREB binding protein gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16237459 619553 Crebbp CREB binding protein gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160519 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10673499 619553 Crebbp CREB binding protein gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:15146178 619553 Crebbp CREB binding protein gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:14517255 619553 Crebbp CREB binding protein gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14517256 619553 Crebbp CREB binding protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12384703 619553 Crebbp CREB binding protein gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16237459 619553 Crebbp CREB binding protein gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9590171 619553 Crebbp CREB binding protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10673499 619553 Crebbp CREB binding protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9294190 619553 Crebbp CREB binding protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10216070 619553 Crebbp CREB binding protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10906457 619553 Crebbp CREB binding protein gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20211216 MGI PMID:9294190 619553 Crebbp CREB binding protein gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14517255 619553 Crebbp CREB binding protein gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16237459 619553 Crebbp CREB binding protein gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14517255 619553 Crebbp CREB binding protein gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16237459 619553 Crebbp CREB binding protein gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:21289174 619553 Crebbp CREB binding protein gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:26730956 619553 Crebbp CREB binding protein gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:9949198 619553 Crebbp CREB binding protein gene MP:0014440 increased response to leptin IAGP N RGD:5509061 20240523 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:11818964 619553 Crebbp CREB binding protein gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:26730956 619555 Cd36 CD36 molecule gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17507371 619555 Cd36 CD36 molecule gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20180301 MGI PMID:25596128 619555 Cd36 CD36 molecule gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 619555 Cd36 CD36 molecule gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 619555 Cd36 CD36 molecule gene MP:0000288 abnormal pericardium morphology IAGP N RGD:5509061 20141003 MGI PMID:16061696 619555 Cd36 CD36 molecule gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:12746501 619555 Cd36 CD36 molecule gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:15023869 619555 Cd36 CD36 molecule gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20160414 MGI PMID:23948483 619555 Cd36 CD36 molecule gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:17507371 619555 Cd36 CD36 molecule gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 619555 Cd36 CD36 molecule gene MP:0000599 enlarged liver IEA N RGD:5509061 20210520 MGI 619555 Cd36 CD36 molecule gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:18242221 619555 Cd36 CD36 molecule gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 619555 Cd36 CD36 molecule gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 619555 Cd36 CD36 molecule gene MP:0000774 decreased brain size IEA N RGD:5509061 20210520 MGI 619555 Cd36 CD36 molecule gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:12823473 619555 Cd36 CD36 molecule gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20191212 MGI PMID:18288886 619555 Cd36 CD36 molecule gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12923231 619555 Cd36 CD36 molecule gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17440173 619555 Cd36 CD36 molecule gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17507371 619555 Cd36 CD36 molecule gene MP:0001432 abnormal food preference IAGP N RGD:5509061 20141003 MGI PMID:16276419 619555 Cd36 CD36 molecule gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12746501 619555 Cd36 CD36 molecule gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15023869 619555 Cd36 CD36 molecule gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:10772649 619555 Cd36 CD36 molecule gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:12923231 619555 Cd36 CD36 molecule gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10383407 619555 Cd36 CD36 molecule gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12923231 619555 Cd36 CD36 molecule gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12923231 619555 Cd36 CD36 molecule gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10383407 619555 Cd36 CD36 molecule gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12746501 619555 Cd36 CD36 molecule gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:17507371 619555 Cd36 CD36 molecule gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17507371 619555 Cd36 CD36 molecule gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20180301 MGI PMID:25596128 619555 Cd36 CD36 molecule gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:16061696 619555 Cd36 CD36 molecule gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:18097024 619555 Cd36 CD36 molecule gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:18097024 619555 Cd36 CD36 molecule gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20161208 MGI PMID:27145700 619555 Cd36 CD36 molecule gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 619555 Cd36 CD36 molecule gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12923231 619555 Cd36 CD36 molecule gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20160414 MGI PMID:23948483 619555 Cd36 CD36 molecule gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20180301 MGI PMID:25596128 619555 Cd36 CD36 molecule gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10383407 619555 Cd36 CD36 molecule gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16061696 619555 Cd36 CD36 molecule gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210520 MGI 619555 Cd36 CD36 molecule gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15690042 619555 Cd36 CD36 molecule gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:15690042 619555 Cd36 CD36 molecule gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10772649 619555 Cd36 CD36 molecule gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12239221 619555 Cd36 CD36 molecule gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15690042 619555 Cd36 CD36 molecule gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:18097024 619555 Cd36 CD36 molecule gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:12923231 619555 Cd36 CD36 molecule gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:17440173 619555 Cd36 CD36 molecule gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10772649 619555 Cd36 CD36 molecule gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180301 MGI PMID:25596128 619555 Cd36 CD36 molecule gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:17507371 619555 Cd36 CD36 molecule gene MP:0002833 increased heart weight IEA N RGD:5509061 20210826 MGI 619555 Cd36 CD36 molecule gene MP:0002865 increased growth rate IAGP N RGD:5509061 20141003 MGI PMID:10772649 619555 Cd36 CD36 molecule gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:12923231 619555 Cd36 CD36 molecule gene MP:0003664 ocular pterygium IAGP N RGD:5509061 20141003 MGI PMID:15690042 619555 Cd36 CD36 molecule gene MP:0003665 endophthalmitis IAGP N RGD:5509061 20141003 MGI PMID:15690042 619555 Cd36 CD36 molecule gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17537546 619555 Cd36 CD36 molecule gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:10772649 619555 Cd36 CD36 molecule gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 619555 Cd36 CD36 molecule gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:12923231 619555 Cd36 CD36 molecule gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:17440173 619555 Cd36 CD36 molecule gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10383407 619555 Cd36 CD36 molecule gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10772649 619555 Cd36 CD36 molecule gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:17440173 619555 Cd36 CD36 molecule gene MP:0004220 abnormal peripheral nervous system regeneration IAGP N RGD:5509061 20141003 MGI PMID:12823473 619555 Cd36 CD36 molecule gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18097024 619555 Cd36 CD36 molecule gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:16061696 619555 Cd36 CD36 molecule gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:16061696 619555 Cd36 CD36 molecule gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10383407 619555 Cd36 CD36 molecule gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10383407 619555 Cd36 CD36 molecule gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12923231 619555 Cd36 CD36 molecule gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:10383407 619555 Cd36 CD36 molecule gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12923231 619555 Cd36 CD36 molecule gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12923231 619555 Cd36 CD36 molecule gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20160414 MGI PMID:23948483 619555 Cd36 CD36 molecule gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17440173 619555 Cd36 CD36 molecule gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:10772649 619555 Cd36 CD36 molecule gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:17507371 619555 Cd36 CD36 molecule gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:12923231 619555 Cd36 CD36 molecule gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:17440173 619555 Cd36 CD36 molecule gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17440173 619555 Cd36 CD36 molecule gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180301 MGI PMID:25596128 619555 Cd36 CD36 molecule gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17440173 619555 Cd36 CD36 molecule gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210520 MGI 619555 Cd36 CD36 molecule gene MP:0006238 abnormal choriocapillaris morphology IAGP N RGD:5509061 20191212 MGI PMID:18288886 619555 Cd36 CD36 molecule gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18097024 619555 Cd36 CD36 molecule gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18097024 619555 Cd36 CD36 molecule gene MP:0008243 abnormal macrophage derived foam cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10772649 619555 Cd36 CD36 molecule gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17440173 619555 Cd36 CD36 molecule gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18097024 619555 Cd36 CD36 molecule gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:18097024 619555 Cd36 CD36 molecule gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20191212 MGI PMID:18288886 619555 Cd36 CD36 molecule gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20191212 MGI PMID:18288886 619555 Cd36 CD36 molecule gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16061696 619555 Cd36 CD36 molecule gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20191212 MGI PMID:18288886 619555 Cd36 CD36 molecule gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:16061696 619555 Cd36 CD36 molecule gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:16061696 619555 Cd36 CD36 molecule gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:12239221 619555 Cd36 CD36 molecule gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20141003 MGI PMID:18097024 619555 Cd36 CD36 molecule gene MP:0008961 abnormal basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:17440173 619555 Cd36 CD36 molecule gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12923231 619555 Cd36 CD36 molecule gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18242221 619555 Cd36 CD36 molecule gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15690042 619555 Cd36 CD36 molecule gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16061696 619555 Cd36 CD36 molecule gene MP:0010148 abnormal exocrine pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:16276419 619555 Cd36 CD36 molecule gene MP:0010360 decreased liver free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18242221 619555 Cd36 CD36 molecule gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20180301 MGI PMID:25596128 619555 Cd36 CD36 molecule gene MP:0010695 abnormal blood pressure regulation IAGP N RGD:5509061 20141003 MGI PMID:11988484 619555 Cd36 CD36 molecule gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12823473 619555 Cd36 CD36 molecule gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180301 MGI PMID:25596128 619555 Cd36 CD36 molecule gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20240229 MGI PMID:25596128 619555 Cd36 CD36 molecule gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20190815 MGI PMID:10383407 619555 Cd36 CD36 molecule gene MP:0013758 increased intestinal glucose absorption IAGP N RGD:5509061 20191031 MGI PMID:17507371 619555 Cd36 CD36 molecule gene MP:0014072 decreased cardiac muscle glycogen level IAGP N RGD:5509061 20190815 MGI PMID:12746501 619555 Cd36 CD36 molecule gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:23948483 619555 Cd36 CD36 molecule gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20180301 MGI PMID:25596128 619555 Cd36 CD36 molecule gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:12746501 619555 Cd36 CD36 molecule gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:17440173 619555 Cd36 CD36 molecule gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:18431509 619555 Cd36 CD36 molecule gene MP:0031417 decreased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:12746501 619555 Cd36 CD36 molecule gene MP:0031417 decreased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:23948483 619555 Cd36 CD36 molecule gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:25596128 619559 Asns asparagine synthetase gene MP:0000774 decreased brain size IAGP N RGD:5509061 20161124 MGI PMID:24139043 619559 Asns asparagine synthetase gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20161124 MGI PMID:24139043 619559 Asns asparagine synthetase gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 619559 Asns asparagine synthetase gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20160804 MGI 619559 Asns asparagine synthetase gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 619559 Asns asparagine synthetase gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20161124 MGI PMID:24139043 619559 Asns asparagine synthetase gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20161124 MGI PMID:24139043 619559 Asns asparagine synthetase gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:24139043 619559 Asns asparagine synthetase gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:24139043 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:23776632 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:10943842 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10973481 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15572667 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:12593847 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17468755 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:21768366 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:10943842 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:21768366 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:10943842 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21768366 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:17468755 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17468755 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23776632 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23776632 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10943842 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:10973481 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:10973481 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:10943842 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17468755 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17468755 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17468755 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17158963 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20170309 MGI PMID:26377476 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17158963 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17468755 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15572667 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17468755 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:23776632 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:15572667 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:23102580 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:12593847 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:21768366 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:17468755 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:23776632 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15572667 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15572667 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:10973481 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:23776632 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003436 decreased susceptibility to induced arthritis IEA N RGD:5509061 20111116 MGI 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15870258 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21768366 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:23776632 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:10943842 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21768366 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10943842 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10973481 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21768366 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:10973481 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17304211 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:15572667 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:23776632 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IEA N RGD:5509061 20111116 MGI 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0004882 enlarged lung IAGP N RGD:5509061 20141003 MGI PMID:17468755 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21768366 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:19011223 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19011223 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15572667 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:19011223 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19619499 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10973481 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:19619499 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0006372 impaired placental function IAGP N RGD:5509061 20141003 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17468755 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:23776632 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17468755 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0008088 abnormal T-helper 1 cell differentiation IEA N RGD:5509061 20111116 MGI 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0008092 abnormal T-helper 2 cell differentiation IEA N RGD:5509061 20111116 MGI 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0008561 decreased tumor necrosis factor secretion IEA N RGD:5509061 20111116 MGI 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:19011223 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19011223 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0008660 increased interleukin-10 secretion IEA N RGD:5509061 20111116 MGI 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10943842 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10973481 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17855341 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15572667 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:21768366 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0010221 abnormal T-helper 17 cell differentiation IEA N RGD:5509061 20111116 MGI 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17468755 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:21768366 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21768366 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21768366 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21768366 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10704466 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10973481 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15572667 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10943842 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21768366 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10943842 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20141003 MGI PMID:21768366 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:17304211 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19619499 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19619499 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:10973481 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0014012 abnormal cranial blood vasculature morphology IAGP N RGD:5509061 20240404 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0030947 increased myoblast proliferation IAGP N RGD:5509061 20190725 MGI PMID:17304211 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0030959 abnormal myoblast fusion IAGP N RGD:5509061 20190725 MGI PMID:17304211 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0031611 decreased fetal cardiomyocyte number IAGP N RGD:5509061 20240404 MGI PMID:10949032 619565 Mapk14 mitogen-activated protein kinase 14 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15572667 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0000087 absent mandible IAGP N RGD:5509061 20150910 MGI PMID:18952847 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0000097 short maxilla IAGP N RGD:5509061 20150910 MGI PMID:18952847 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20150910 MGI PMID:18952847 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20150910 MGI PMID:18952847 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20150910 MGI PMID:18952847 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20150910 MGI PMID:18952847 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0000705 athymia IAGP N RGD:5509061 20150910 MGI PMID:18952847 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:16226508 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16226508 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20150910 MGI PMID:18952847 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20150910 MGI PMID:18952847 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12062026 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17709754 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:19017799 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17709754 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21514245 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20150910 MGI PMID:18952847 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0002798 abnormal active avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:12062026 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:12062026 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16081808 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0003808 increased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:19017799 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:16226508 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20368360 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16081808 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:16226508 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10558995 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16226508 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16226508 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10558995 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0005432 abnormal pro-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18356083 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20150910 MGI PMID:18952847 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20150910 MGI PMID:18952847 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20368360 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18356083 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0008233 abnormal pro-B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18356083 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0008658 decreased interleukin-1 beta secretion IEA N RGD:5509061 20150702 MGI 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21514245 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0009905 absent tongue IAGP N RGD:5509061 20150910 MGI PMID:18952847 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0010283 decreased classified tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21514245 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20150910 MGI PMID:18952847 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19017799 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20368360 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0012269 nuchal edema IAGP N RGD:5509061 20141003 MGI PMID:19017799 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:20368360 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:11160759 619571 Mapk3 mitogen-activated protein kinase 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:12062026 619573 Slc22a6 solute carrier family 22 (organic anion transporter), member 6 gene MP:0004955 increased thymus weight IEA N RGD:5509061 20111116 MGI 619573 Slc22a6 solute carrier family 22 (organic anion transporter), member 6 gene MP:0006272 abnormal urine organic anion level IAGP N RGD:5509061 20141003 MGI PMID:16354673 619573 Slc22a6 solute carrier family 22 (organic anion transporter), member 6 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16354673 619573 Slc22a6 solute carrier family 22 (organic anion transporter), member 6 gene MP:0011424 decreased urine uric acid level IAGP N RGD:5509061 20141003 MGI PMID:18270321 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17623040 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:23152496 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:17623040 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:17623040 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21212098 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12915482 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17116640 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23152496 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17883413 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:12915482 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001391 abnormal tail movements IAGP N RGD:5509061 20141003 MGI PMID:17623040 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12930822 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:24075852 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:17623040 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:12915482 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17883413 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17883413 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15249681 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:17623040 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:17883413 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:12915482 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:12930822 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:17116640 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:18691389 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:24075852 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17623040 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12930822 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20141003 MGI PMID:17623040 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:17883413 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17412759 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21768369 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20141003 MGI PMID:18691389 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17623040 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:17623040 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:18691389 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:17623040 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:21768369 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:17623040 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12915482 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15249681 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:18691389 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20141003 MGI PMID:17623040 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:21768369 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:18691389 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:17412759 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:21212098 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:23152496 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20150402 MGI PMID:25609609 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:23152496 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:17412759 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:23152496 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:23152496 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:23307929 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17883413 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23152496 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:24075852 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:17412759 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:17412759 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:12915482 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:18691389 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:21376232 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:23152496 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0011975 neuronal cytoplasmic inclusions IAGP N RGD:5509061 20150402 MGI PMID:25609609 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:15249681 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20141003 MGI PMID:17116640 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20160304 MGI PMID:23152496 62089 Prkn parkin RBR E3 ubiquitin protein ligase gene MP:0020543 decreased substantia nigra size IAGP N RGD:5509061 20180301 MGI PMID:17623040 62090 P2ry4 pyrimidinergic receptor P2Y, G-protein coupled, 4 gene MP:0000501 abnormal digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:12644577 62090 P2ry4 pyrimidinergic receptor P2Y, G-protein coupled, 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12644577 62091 Kcnq4 potassium voltage-gated channel, subfamily Q, member 4 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16437162 62091 Kcnq4 potassium voltage-gated channel, subfamily Q, member 4 gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16437162 62091 Kcnq4 potassium voltage-gated channel, subfamily Q, member 4 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:16437162 62091 Kcnq4 potassium voltage-gated channel, subfamily Q, member 4 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:16437162 62091 Kcnq4 potassium voltage-gated channel, subfamily Q, member 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16437162 62092 Htr2a 5-hydroxytryptamine (serotonin) receptor 2A gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11960784 62092 Htr2a 5-hydroxytryptamine (serotonin) receptor 2A gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16873667 62092 Htr2a 5-hydroxytryptamine (serotonin) receptor 2A gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16873667 62092 Htr2a 5-hydroxytryptamine (serotonin) receptor 2A gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:16873667 62092 Htr2a 5-hydroxytryptamine (serotonin) receptor 2A gene MP:0008802 abnormal intestinal smooth muscle morphology IAGP N RGD:5509061 20150312 MGI PMID:11960784 62092 Htr2a 5-hydroxytryptamine (serotonin) receptor 2A gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20150312 MGI PMID:11960784 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10944220 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0000296 absent trabeculae carneae IAGP N RGD:5509061 20141003 MGI PMID:10944220 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10944220 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12244304 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10944220 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:10944220 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:10944220 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:10944220 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200402 MGI PMID:31806625 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:10944220 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:10944220 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:10944220 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10944220 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:10944220 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12244304 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20200402 MGI PMID:31806625 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20160421 MGI 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0010759 decreased right ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:12244304 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10944220 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0011092 embryonic lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10944220 62093 Htr2b 5-hydroxytryptamine (serotonin) receptor 2B gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20200402 MGI PMID:31806625 62096 Map6 microtubule-associated protein 6 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:12231625 62096 Map6 microtubule-associated protein 6 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20151119 MGI PMID:23002183 62096 Map6 microtubule-associated protein 6 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12231625 62096 Map6 microtubule-associated protein 6 gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:12231625 62096 Map6 microtubule-associated protein 6 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:12231625 62096 Map6 microtubule-associated protein 6 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12231625 62096 Map6 microtubule-associated protein 6 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20151119 MGI PMID:23002183 62096 Map6 microtubule-associated protein 6 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20220421 MGI PMID:23002183 62096 Map6 microtubule-associated protein 6 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12231625 62096 Map6 microtubule-associated protein 6 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:12231625 62096 Map6 microtubule-associated protein 6 gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:12231625 62096 Map6 microtubule-associated protein 6 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:12231625 62096 Map6 microtubule-associated protein 6 gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:12231625 62096 Map6 microtubule-associated protein 6 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20151119 MGI PMID:23002183 62096 Map6 microtubule-associated protein 6 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20151119 MGI PMID:23002183 62096 Map6 microtubule-associated protein 6 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12231625 62096 Map6 microtubule-associated protein 6 gene MP:0013894 abnormal behavioral response to amphetamine IAGP N RGD:5509061 20151119 MGI PMID:23002183 62097 Fgf7 fibroblast growth factor 7 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:9876183 62097 Fgf7 fibroblast growth factor 7 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16304055 62097 Fgf7 fibroblast growth factor 7 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20240523 MGI 62097 Fgf7 fibroblast growth factor 7 gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20240523 MGI 62097 Fgf7 fibroblast growth factor 7 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20210422 MGI 62097 Fgf7 fibroblast growth factor 7 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:8566750 62097 Fgf7 fibroblast growth factor 7 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:8566750 62097 Fgf7 fibroblast growth factor 7 gene MP:0001523 impaired righting response IEA N RGD:5509061 20210422 MGI 62097 Fgf7 fibroblast growth factor 7 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:16304055 62097 Fgf7 fibroblast growth factor 7 gene MP:0002546 mydriasis IEA N RGD:5509061 20210422 MGI 62097 Fgf7 fibroblast growth factor 7 gene MP:0002881 long hair IAGP N RGD:5509061 20141003 MGI PMID:12917328 62097 Fgf7 fibroblast growth factor 7 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:20505669 62097 Fgf7 fibroblast growth factor 7 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:9876183 62097 Fgf7 fibroblast growth factor 7 gene MP:0003846 matted coat IAGP N RGD:5509061 20141003 MGI PMID:8566750 62097 Fgf7 fibroblast growth factor 7 gene MP:0003849 greasy coat IAGP N RGD:5509061 20141003 MGI PMID:8566750 62097 Fgf7 fibroblast growth factor 7 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20505669 62097 Fgf7 fibroblast growth factor 7 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:20505669 62097 Fgf7 fibroblast growth factor 7 gene MP:0004793 abnormal synaptic vesicle clustering IAGP N RGD:5509061 20141003 MGI PMID:20505669 62097 Fgf7 fibroblast growth factor 7 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:9876183 62097 Fgf7 fibroblast growth factor 7 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:16304055 62097 Fgf7 fibroblast growth factor 7 gene MP:0006241 abnormal placement of pupils IEA N RGD:5509061 20220811 MGI 62097 Fgf7 fibroblast growth factor 7 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20210422 MGI 62097 Fgf7 fibroblast growth factor 7 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:9876183 62097 Fgf7 fibroblast growth factor 7 gene MP:0011331 abnormal papillary duct morphology IAGP N RGD:5509061 20141003 MGI PMID:9876183 62097 Fgf7 fibroblast growth factor 7 gene MP:0011333 abnormal kidney inner medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:9876183 62097 Fgf7 fibroblast growth factor 7 gene MP:0011360 kidney cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9876183 62097 Fgf7 fibroblast growth factor 7 gene MP:0011565 kidney papillary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9876183 62097 Fgf7 fibroblast growth factor 7 gene MP:0011843 abnormal kidney collecting duct epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9876183 62097 Fgf7 fibroblast growth factor 7 gene MP:0011999 abnormal tail length IEA N RGD:5509061 20210422 MGI 62097 Fgf7 fibroblast growth factor 7 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:20505669 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:20484637 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20180621 MGI PMID:26951213 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20180621 MGI PMID:29132416 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:20484637 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20180621 MGI PMID:26951213 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20180621 MGI PMID:29132416 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20484637 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20180621 MGI PMID:26951213 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0001070 abnormal abducens nerve morphology IAGP N RGD:5509061 20180621 MGI PMID:29132416 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20484637 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:10400672 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10400672 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20180621 MGI PMID:26951213 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10400672 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:20484637 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20180621 MGI PMID:26951213 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20180621 MGI PMID:29132416 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0002316 anoxia IAGP N RGD:5509061 20141003 MGI PMID:10400672 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20180621 MGI PMID:29132416 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10400672 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20484637 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180621 MGI PMID:26951213 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180621 MGI PMID:29132416 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20141003 MGI PMID:20484637 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20180621 MGI PMID:26951213 62098 Ecel1 endothelin converting enzyme-like 1 gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20180621 MGI PMID:29132416 62099 Foxm1 forkhead box M1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9843684 62099 Foxm1 forkhead box M1 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17366632 62099 Foxm1 forkhead box M1 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15817462 62099 Foxm1 forkhead box M1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12482952 62099 Foxm1 forkhead box M1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15082532 62099 Foxm1 forkhead box M1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9843684 62099 Foxm1 forkhead box M1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:15817462 62099 Foxm1 forkhead box M1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:21199796 62099 Foxm1 forkhead box M1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15531365 62099 Foxm1 forkhead box M1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:9843684 62099 Foxm1 forkhead box M1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21199796 62099 Foxm1 forkhead box M1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20150618 MGI PMID:16556734 62099 Foxm1 forkhead box M1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9843684 62099 Foxm1 forkhead box M1 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:17366632 62099 Foxm1 forkhead box M1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:15531365 62099 Foxm1 forkhead box M1 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:9843684 62099 Foxm1 forkhead box M1 gene MP:0002658 abnormal liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:12482952 62099 Foxm1 forkhead box M1 gene MP:0002844 aortic hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15817462 62099 Foxm1 forkhead box M1 gene MP:0002975 vascular smooth muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15817462 62099 Foxm1 forkhead box M1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15531365 62099 Foxm1 forkhead box M1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15082532 62099 Foxm1 forkhead box M1 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20150618 MGI PMID:16556734 62099 Foxm1 forkhead box M1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20150618 MGI PMID:16556734 62099 Foxm1 forkhead box M1 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20150618 MGI PMID:16556734 62099 Foxm1 forkhead box M1 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:15817462 62099 Foxm1 forkhead box M1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15817462 62099 Foxm1 forkhead box M1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17366632 62099 Foxm1 forkhead box M1 gene MP:0004181 abnormal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15817462 62099 Foxm1 forkhead box M1 gene MP:0004391 abnormal respiratory conducting tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15082532 62099 Foxm1 forkhead box M1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:21199796 62099 Foxm1 forkhead box M1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15082532 62099 Foxm1 forkhead box M1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:15531365 62099 Foxm1 forkhead box M1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20150618 MGI PMID:16556734 62099 Foxm1 forkhead box M1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20150618 MGI PMID:16556734 62099 Foxm1 forkhead box M1 gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20150618 MGI PMID:16556734 62099 Foxm1 forkhead box M1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20150618 MGI PMID:16556734 62099 Foxm1 forkhead box M1 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20240404 MGI PMID:17366632 62099 Foxm1 forkhead box M1 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17366632 62099 Foxm1 forkhead box M1 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20141003 MGI PMID:15531365 62099 Foxm1 forkhead box M1 gene MP:0009109 decreased pancreas weight IAGP N RGD:5509061 20150618 MGI PMID:16556734 62099 Foxm1 forkhead box M1 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20150618 MGI PMID:16556734 62099 Foxm1 forkhead box M1 gene MP:0009148 pancreas necrosis IAGP N RGD:5509061 20150618 MGI PMID:16556734 62099 Foxm1 forkhead box M1 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20150618 MGI PMID:16556734 62099 Foxm1 forkhead box M1 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20150618 MGI PMID:16556734 62099 Foxm1 forkhead box M1 gene MP:0009497 abnormal intrahepatic bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:15531365 62099 Foxm1 forkhead box M1 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0010266 decreased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15082532 62099 Foxm1 forkhead box M1 gene MP:0010439 abnormal hepatic vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15531365 62099 Foxm1 forkhead box M1 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:17366632 62099 Foxm1 forkhead box M1 gene MP:0010580 decreased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:17366632 62099 Foxm1 forkhead box M1 gene MP:0010617 thick mitral valve cusps IAGP N RGD:5509061 20240404 MGI PMID:17366632 62099 Foxm1 forkhead box M1 gene MP:0010816 decreased type I pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0010827 small lung saccule IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0010889 small alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0011018 pulmonary hyaline membrane formation IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15531365 62099 Foxm1 forkhead box M1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15531365 62099 Foxm1 forkhead box M1 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17366632 62099 Foxm1 forkhead box M1 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:19033457 62099 Foxm1 forkhead box M1 gene MP:0011148 decreased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:15817462 62099 Foxm1 forkhead box M1 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20240404 MGI PMID:17366632 62099 Foxm1 forkhead box M1 gene MP:0011648 thick heart valve cusps IAGP N RGD:5509061 20141003 MGI PMID:17366632 62099 Foxm1 forkhead box M1 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20150618 MGI PMID:16556734 62099 Foxm1 forkhead box M1 gene MP:0012240 abnormal hepatoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:15531365 62099 Foxm1 forkhead box M1 gene MP:0012243 decreased hepatoblast number IAGP N RGD:5509061 20141003 MGI PMID:15531365 62099 Foxm1 forkhead box M1 gene MP:0012246 abnormal hepatic cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15531365 62099 Foxm1 forkhead box M1 gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:9843684 62099 Foxm1 forkhead box M1 gene MP:0031609 increased fetal cardiomyocyte size IAGP N RGD:5509061 20240404 MGI PMID:17366632 62099 Foxm1 forkhead box M1 gene MP:0031611 decreased fetal cardiomyocyte number IAGP N RGD:5509061 20240404 MGI PMID:17366632 62100 Faah fatty acid amide hydrolase gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20160929 MGI PMID:25731744 62100 Faah fatty acid amide hydrolase gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:16571781 62100 Faah fatty acid amide hydrolase gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20160929 MGI PMID:25731744 62100 Faah fatty acid amide hydrolase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11470906 62100 Faah fatty acid amide hydrolase gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11470906 62100 Faah fatty acid amide hydrolase gene MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:11470906 62100 Faah fatty acid amide hydrolase gene MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:16448676 62100 Faah fatty acid amide hydrolase gene MP:0001987 alcohol preference IAGP N RGD:5509061 20141003 MGI PMID:16448676 62100 Faah fatty acid amide hydrolase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16571781 62100 Faah fatty acid amide hydrolase gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:16571781 62100 Faah fatty acid amide hydrolase gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 62100 Faah fatty acid amide hydrolase gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 62100 Faah fatty acid amide hydrolase gene MP:0002822 catalepsy IAGP N RGD:5509061 20141003 MGI PMID:11470906 62100 Faah fatty acid amide hydrolase gene MP:0002863 improved righting response IAGP N RGD:5509061 20141003 MGI PMID:16448676 62100 Faah fatty acid amide hydrolase gene MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:16448676 62100 Faah fatty acid amide hydrolase gene MP:0004166 abnormal limbic system morphology IAGP N RGD:5509061 20160929 MGI PMID:25731744 62100 Faah fatty acid amide hydrolase gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:11470906 62100 Faah fatty acid amide hydrolase gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:16448676 62100 Faah fatty acid amide hydrolase gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230119 MGI 62100 Faah fatty acid amide hydrolase gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11470906 62100 Faah fatty acid amide hydrolase gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20230119 MGI 62100 Faah fatty acid amide hydrolase gene MP:0012319 fast extinction of fear memory IAGP N RGD:5509061 20160929 MGI PMID:25731744 62100 Faah fatty acid amide hydrolase gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230119 MGI 62100 Faah fatty acid amide hydrolase gene MP:0030764 increased anandamide level IAGP N RGD:5509061 20180927 MGI PMID:25731744 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0000392 accelerated hair follicle regression IAGP N RGD:5509061 20141003 MGI PMID:10069331 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0000392 accelerated hair follicle regression IAGP N RGD:5509061 20141003 MGI PMID:10702420 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0001036 small submandibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:10069331 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0001037 abnormal parasympathetic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17585017 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:10702420 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10069331 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17585017 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0001337 dry eyes IAGP N RGD:5509061 20141003 MGI PMID:10069331 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:10069331 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0001500 decreased kindling response IAGP N RGD:5509061 20141003 MGI PMID:10069331 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:12952919 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0004141 abnormal enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17585017 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:17585017 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0008313 abnormal parasympathetic postganglionic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10069331 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:12952919 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12952919 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:12952919 62101 Gfra2 glial cell line derived neurotrophic factor family receptor alpha 2 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:12952919 62102 Ctsk cathepsin K gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:16753017 62102 Ctsk cathepsin K gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15664014 62102 Ctsk cathepsin K gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20151112 MGI PMID:25811986 62102 Ctsk cathepsin K gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:16753017 62102 Ctsk cathepsin K gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:23341620 62102 Ctsk cathepsin K gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:17803905 62102 Ctsk cathepsin K gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:21876000 62102 Ctsk cathepsin K gene MP:0000066 osteoporosis IAGP N RGD:5509061 20160407 MGI PMID:23908115 62102 Ctsk cathepsin K gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:15664014 62102 Ctsk cathepsin K gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:16753017 62102 Ctsk cathepsin K gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:23341620 62102 Ctsk cathepsin K gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:9811821 62102 Ctsk cathepsin K gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20151112 MGI PMID:25811986 62102 Ctsk cathepsin K gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20151112 MGI PMID:25811986 62102 Ctsk cathepsin K gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15664014 62102 Ctsk cathepsin K gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16753017 62102 Ctsk cathepsin K gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23341620 62102 Ctsk cathepsin K gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9811821 62102 Ctsk cathepsin K gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:23341620 62102 Ctsk cathepsin K gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21876000 62102 Ctsk cathepsin K gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0000578 ulcerated autopod IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:17068745 62102 Ctsk cathepsin K gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12782676 62102 Ctsk cathepsin K gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 62102 Ctsk cathepsin K gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:15161653 62102 Ctsk cathepsin K gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:16753017 62102 Ctsk cathepsin K gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:17803905 62102 Ctsk cathepsin K gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:23321671 62102 Ctsk cathepsin K gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:23341620 62102 Ctsk cathepsin K gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:9811821 62102 Ctsk cathepsin K gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20151112 MGI PMID:25811986 62102 Ctsk cathepsin K gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20170518 MGI PMID:27777970 62102 Ctsk cathepsin K gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20151112 MGI PMID:25811986 62102 Ctsk cathepsin K gene MP:0002764 short tibia IEA N RGD:5509061 20160421 MGI 62102 Ctsk cathepsin K gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:16753017 62102 Ctsk cathepsin K gene MP:0003173 decreased lysosomal enzyme secretion IAGP N RGD:5509061 20170518 MGI PMID:27777970 62102 Ctsk cathepsin K gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23341620 62102 Ctsk cathepsin K gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16753017 62102 Ctsk cathepsin K gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:9811821 62102 Ctsk cathepsin K gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16753017 62102 Ctsk cathepsin K gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20160407 MGI PMID:23908115 62102 Ctsk cathepsin K gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:16753017 62102 Ctsk cathepsin K gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9811821 62102 Ctsk cathepsin K gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12782676 62102 Ctsk cathepsin K gene MP:0004697 abnormal thyroid follicular cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12782676 62102 Ctsk cathepsin K gene MP:0004913 absent mandibular angle IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0004945 abnormal bone resorption IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:15664014 62102 Ctsk cathepsin K gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:23341620 62102 Ctsk cathepsin K gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20170518 MGI PMID:27777970 62102 Ctsk cathepsin K gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:15664014 62102 Ctsk cathepsin K gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:16753017 62102 Ctsk cathepsin K gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17803905 62102 Ctsk cathepsin K gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:21876000 62102 Ctsk cathepsin K gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:23321671 62102 Ctsk cathepsin K gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:23321671 62102 Ctsk cathepsin K gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20170518 MGI PMID:27777970 62102 Ctsk cathepsin K gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:17803905 62102 Ctsk cathepsin K gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:21876000 62102 Ctsk cathepsin K gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:21876000 62102 Ctsk cathepsin K gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20170518 MGI PMID:27777970 62102 Ctsk cathepsin K gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:16753017 62102 Ctsk cathepsin K gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:23321671 62102 Ctsk cathepsin K gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20170518 MGI PMID:27777970 62102 Ctsk cathepsin K gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:12782676 62102 Ctsk cathepsin K gene MP:0005471 decreased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:12782676 62102 Ctsk cathepsin K gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:12782676 62102 Ctsk cathepsin K gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15161653 62102 Ctsk cathepsin K gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20151112 MGI PMID:25811986 62102 Ctsk cathepsin K gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:9811821 62102 Ctsk cathepsin K gene MP:0008162 increased diameter of tibia IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:23321671 62102 Ctsk cathepsin K gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21876000 62102 Ctsk cathepsin K gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:23321671 62102 Ctsk cathepsin K gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 62102 Ctsk cathepsin K gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20160407 MGI PMID:23908115 62102 Ctsk cathepsin K gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23321671 62102 Ctsk cathepsin K gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23341620 62102 Ctsk cathepsin K gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:16753017 62102 Ctsk cathepsin K gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23321671 62102 Ctsk cathepsin K gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23341620 62102 Ctsk cathepsin K gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20170518 MGI PMID:27777970 62102 Ctsk cathepsin K gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20160407 MGI PMID:23908115 62102 Ctsk cathepsin K gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:16753017 62102 Ctsk cathepsin K gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:23321671 62102 Ctsk cathepsin K gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20170518 MGI PMID:27777970 62102 Ctsk cathepsin K gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:21876000 62102 Ctsk cathepsin K gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:23321671 62102 Ctsk cathepsin K gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20151112 MGI PMID:25811986 62102 Ctsk cathepsin K gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:23321671 62102 Ctsk cathepsin K gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:23341620 62102 Ctsk cathepsin K gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20170518 MGI PMID:27777970 62102 Ctsk cathepsin K gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:21876000 62102 Ctsk cathepsin K gene MP:0010924 abnormal osteoid morphology IAGP N RGD:5509061 20160407 MGI PMID:23908115 62102 Ctsk cathepsin K gene MP:0010932 increased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:23321671 62102 Ctsk cathepsin K gene MP:0010964 increased compact bone volume IAGP N RGD:5509061 20141003 MGI PMID:23321671 62102 Ctsk cathepsin K gene MP:0010967 increased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:16753017 62102 Ctsk cathepsin K gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20160407 MGI PMID:23908115 62102 Ctsk cathepsin K gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20170518 MGI PMID:27777970 62102 Ctsk cathepsin K gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:17803905 62102 Ctsk cathepsin K gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:23321671 62102 Ctsk cathepsin K gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160616 MGI PMID:17803905 62102 Ctsk cathepsin K gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:23908115 62102 Ctsk cathepsin K gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20170518 MGI PMID:27777970 62102 Ctsk cathepsin K gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:23321671 62102 Ctsk cathepsin K gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:17803905 62102 Ctsk cathepsin K gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20170518 MGI PMID:27777970 62102 Ctsk cathepsin K gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0030279 thin neurocranium IAGP N RGD:5509061 20171102 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0030388 large fontanelles IAGP N RGD:5509061 20171207 MGI PMID:17210673 62102 Ctsk cathepsin K gene MP:0031312 spondylolysis IAGP N RGD:5509061 20211104 MGI PMID:17210673 62103 Fcgrt Fc fragment of IgG receptor and transporter gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:19188594 62103 Fcgrt Fc fragment of IgG receptor and transporter gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12566415 62103 Fcgrt Fc fragment of IgG receptor and transporter gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12646614 62103 Fcgrt Fc fragment of IgG receptor and transporter gene MP:0002083 premature death IAGP N RGD:5509061 20171214 MGI PMID:21964024 62103 Fcgrt Fc fragment of IgG receptor and transporter gene MP:0002965 increased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:12566415 62103 Fcgrt Fc fragment of IgG receptor and transporter gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:12566415 62103 Fcgrt Fc fragment of IgG receptor and transporter gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:19188594 62103 Fcgrt Fc fragment of IgG receptor and transporter gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19188594 62104 Pxmp2 peroxisomal membrane protein 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:19352492 62104 Pxmp2 peroxisomal membrane protein 2 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:19352492 62104 Pxmp2 peroxisomal membrane protein 2 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:19352492 62104 Pxmp2 peroxisomal membrane protein 2 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:19352492 62104 Pxmp2 peroxisomal membrane protein 2 gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:19352492 62104 Pxmp2 peroxisomal membrane protein 2 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19352492 62104 Pxmp2 peroxisomal membrane protein 2 gene MP:0013716 hypolactation IAGP N RGD:5509061 20150611 MGI PMID:19352492 62105 Ftl1 ferritin light polypeptide 1 gene MP:0001396 unidirectional circling IAGP N RGD:5509061 20180301 MGI PMID:25629408 62105 Ftl1 ferritin light polypeptide 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 62105 Ftl1 ferritin light polypeptide 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20200514 MGI 62105 Ftl1 ferritin light polypeptide 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 62105 Ftl1 ferritin light polypeptide 1 gene MP:0004152 abnormal circulating iron level IEA N RGD:5509061 20210520 MGI 62105 Ftl1 ferritin light polypeptide 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20200514 MGI 62105 Ftl1 ferritin light polypeptide 1 gene MP:0005191 head tilt IAGP N RGD:5509061 20180301 MGI PMID:25629408 62105 Ftl1 ferritin light polypeptide 1 gene MP:0008248 abnormal mononuclear phagocyte morphology IAGP N RGD:5509061 20180301 MGI PMID:25629408 62105 Ftl1 ferritin light polypeptide 1 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20180301 MGI PMID:25629408 62105 Ftl1 ferritin light polypeptide 1 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20180301 MGI PMID:25629408 62105 Ftl1 ferritin light polypeptide 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 62105 Ftl1 ferritin light polypeptide 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20180301 MGI PMID:25629408 62105 Ftl1 ferritin light polypeptide 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20180301 MGI PMID:25629408 62105 Ftl1 ferritin light polypeptide 1 gene MP:0011898 abnormal platelet cell number IEA N RGD:5509061 20211021 MGI 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14673138 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000436 abnormal head movements IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:14673138 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000610 cholestasis IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0001512 trunk curl IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0001553 abnormal circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20160609 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14673138 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:14673138 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14673138 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14673138 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12746876 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9382874 62106 Pex2 peroxisomal biogenesis factor 2 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:9382874 62107 Npvf neuropeptide VF precursor gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20240502 MGI PMID:36355189 62107 Npvf neuropeptide VF precursor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20240502 MGI PMID:36355189 62107 Npvf neuropeptide VF precursor gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20240502 MGI PMID:36355189 62107 Npvf neuropeptide VF precursor gene MP:0031392 hypoactivity IAGP N RGD:5509061 20240502 MGI PMID:36355189 62108 Actn4 actinin alpha 4 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0000297 abnormal atrioventricular cushion morphology IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0000445 short snout IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0001014 absent superior cervical ganglion IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 62108 Actn4 actinin alpha 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0002725 abnormal vein morphology IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 62108 Actn4 actinin alpha 4 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:17082197 62108 Actn4 actinin alpha 4 gene MP:0002959 increased urine microalbumin level IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:15208719 62108 Actn4 actinin alpha 4 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0003237 abnormal lens epithelium morphology IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0003266 biliary cyst IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0004666 absent stapedial artery IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0005244 hemopericardium IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0005265 abnormal blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:15208719 62108 Actn4 actinin alpha 4 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15208719 62108 Actn4 actinin alpha 4 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0006093 arteriovenous malformation IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:15208719 62108 Actn4 actinin alpha 4 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15208719 62108 Actn4 actinin alpha 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 62108 Actn4 actinin alpha 4 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20141003 MGI PMID:17082197 62108 Actn4 actinin alpha 4 gene MP:0011826 abnormal lymphocyte chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12782671 62108 Actn4 actinin alpha 4 gene MP:0011864 abnormal podocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:17082197 62108 Actn4 actinin alpha 4 gene MP:0011869 detached podocyte IAGP N RGD:5509061 20141003 MGI PMID:17082197 62108 Actn4 actinin alpha 4 gene MP:0013824 abnormal hypoglossal canal morphology IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0013825 small hypoglossal canal IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0013826 absent hypoglossal canal IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0013875 increased trigeminal neuroma incidence IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0013878 abnormal ductus venosus valve topology IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0013968 multiple persisting craniopharyngeal ducts IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0013975 abnormal coronary sinus connection IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0013992 persistent dorsal ophthalmic artery IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0014018 embryo tumor IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0014021 heterochrony IEA N RGD:5509061 20170504 MGI 62108 Actn4 actinin alpha 4 gene MP:0014023 abnormal intestine placement IEA N RGD:5509061 20170504 MGI 62111 Htr3b 5-hydroxytryptamine (serotonin) receptor 3B gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 62111 Htr3b 5-hydroxytryptamine (serotonin) receptor 3B gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0000603 pale liver IEA N RGD:5509061 20210520 MGI 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20201022 MGI 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:17704211 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20230309 MGI PMID:25382630 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220106 MGI PMID:34910520 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:17704211 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0003057 abnormal epicardium morphology IAGP N RGD:5509061 20141003 MGI PMID:17704211 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210128 MGI 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:17704211 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0004627 abnormal trochanter morphology IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0004848 abnormal liver size IEA N RGD:5509061 20201022 MGI 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0004855 increased ovary weight IAGP N RGD:5509061 20220106 MGI PMID:34910520 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0005131 increased follicle stimulating hormone level IAGP N RGD:5509061 20220106 MGI PMID:34910520 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20230309 MGI PMID:25382630 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20230309 MGI PMID:25382630 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20230309 MGI PMID:25382630 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20230309 MGI PMID:25382630 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:17704211 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0010498 abnormal interventricular septum muscular part morphology IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0010502 ventricle myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17704211 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20230309 MGI PMID:25382630 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12773577 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0021217 abnormal palatal shelf bone ossification IAGP N RGD:5509061 20230309 MGI PMID:25382630 62112 Tgfbr3 transforming growth factor, beta receptor III gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230309 MGI PMID:25382630 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10908613 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:10908613 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:10908613 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10908613 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20151217 MGI PMID:19420365 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0001762 polyuria IAGP N RGD:5509061 20151217 MGI PMID:19420365 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0002607 decreased basophil cell number IEA N RGD:5509061 20231207 MGI 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20151217 MGI PMID:19420365 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0002923 increased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20151217 MGI PMID:19420365 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0003169 abnormal scala media morphology IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0004298 vestibular ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0004331 vestibular saccular macula degeneration IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0004334 utricular macular degeneration IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0004409 abnormal crista ampullaris neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0004410 absent endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:11788352 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0004716 abnormal cochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:10908613 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:10908613 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10908613 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0006021 abnormal Reissner membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11788352 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0006021 abnormal Reissner membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0006025 distended Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20151217 MGI PMID:19420365 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:11788352 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:11788352 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0006403 abnormal cochlear endolymph ionic homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11788352 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17942730 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10908613 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11466414 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12618319 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20151217 MGI PMID:19420365 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20151217 MGI PMID:19420365 62113 Kcnj10 potassium inwardly-rectifying channel, subfamily J, member 10 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11788352 62114 Rnase4 ribonuclease, RNase A family 4 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20241017 MGI PMID:38987259 62114 Rnase4 ribonuclease, RNase A family 4 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20241017 MGI PMID:38987259 62114 Rnase4 ribonuclease, RNase A family 4 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20241017 MGI PMID:38987259 62114 Rnase4 ribonuclease, RNase A family 4 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20241017 MGI PMID:38987259 62115 Kcnj16 potassium inwardly-rectifying channel, subfamily J, member 16 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:21047793 62115 Kcnj16 potassium inwardly-rectifying channel, subfamily J, member 16 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21047793 62116 Tcea2 transcription elongation factor A (SII), 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 62116 Tcea2 transcription elongation factor A (SII), 2 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 62116 Tcea2 transcription elongation factor A (SII), 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 62116 Tcea2 transcription elongation factor A (SII), 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 62117 Chkb choline kinase beta gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:16371353 62117 Chkb choline kinase beta gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:16371353 62117 Chkb choline kinase beta gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:16371353 62117 Chkb choline kinase beta gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:16371353 62117 Chkb choline kinase beta gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:16371353 62117 Chkb choline kinase beta gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20111116 MGI 62117 Chkb choline kinase beta gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16371353 62117 Chkb choline kinase beta gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16371353 62117 Chkb choline kinase beta gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:16371353 62117 Chkb choline kinase beta gene MP:0004355 short radius IEA N RGD:5509061 20111116 MGI 62117 Chkb choline kinase beta gene MP:0004359 short ulna IEA N RGD:5509061 20111116 MGI 62117 Chkb choline kinase beta gene MP:0004361 bowed ulna IAGP N RGD:5509061 20141003 MGI PMID:16371353 62117 Chkb choline kinase beta gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:16371353 62117 Chkb choline kinase beta gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:16371353 62117 Chkb choline kinase beta gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:16371353 62117 Chkb choline kinase beta gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:16371353 62117 Chkb choline kinase beta gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 62118 Kcnab1 potassium voltage-gated channel, shaker-related subfamily, beta member 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10454353 62118 Kcnab1 potassium voltage-gated channel, shaker-related subfamily, beta member 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:14511342 62118 Kcnab1 potassium voltage-gated channel, shaker-related subfamily, beta member 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15530391 62118 Kcnab1 potassium voltage-gated channel, shaker-related subfamily, beta member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15720404 62118 Kcnab1 potassium voltage-gated channel, shaker-related subfamily, beta member 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10454353 62118 Kcnab1 potassium voltage-gated channel, shaker-related subfamily, beta member 1 gene MP:0002969 impaired social transmission of food preference IAGP N RGD:5509061 20141003 MGI PMID:10454353 62118 Kcnab1 potassium voltage-gated channel, shaker-related subfamily, beta member 1 gene MP:0002969 impaired social transmission of food preference IAGP N RGD:5509061 20141003 MGI PMID:14511342 62118 Kcnab1 potassium voltage-gated channel, shaker-related subfamily, beta member 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:15530391 62118 Kcnab1 potassium voltage-gated channel, shaker-related subfamily, beta member 1 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:15662035 62118 Kcnab1 potassium voltage-gated channel, shaker-related subfamily, beta member 1 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20141003 MGI PMID:15530391 62118 Kcnab1 potassium voltage-gated channel, shaker-related subfamily, beta member 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:10454353 62118 Kcnab1 potassium voltage-gated channel, shaker-related subfamily, beta member 1 gene MP:0020340 abnormal inhibitory learning IAGP N RGD:5509061 20160915 MGI PMID:10454353 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20231207 MGI 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11825900 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15720404 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:11825900 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15720404 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:21209188 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:21209188 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11825900 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15720404 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11825900 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21209188 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20231207 MGI 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20141003 MGI PMID:21209188 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20231207 MGI 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21209188 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20231207 MGI 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20231207 MGI 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:15720404 62119 Kcnab2 potassium voltage-gated channel, shaker-related subfamily, beta member 2 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:15720404 62120 Ptma prothymosin alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190131 MGI PMID:28122138 62120 Ptma prothymosin alpha gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210128 MGI 62120 Ptma prothymosin alpha gene MP:0001314 cornea opacity IEA N RGD:5509061 20160421 MGI 62120 Ptma prothymosin alpha gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20190131 MGI PMID:28122138 62120 Ptma prothymosin alpha gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190131 MGI PMID:28122138 62120 Ptma prothymosin alpha gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20190131 MGI PMID:28122138 62120 Ptma prothymosin alpha gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20190131 MGI PMID:28122138 62120 Ptma prothymosin alpha gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20190131 MGI PMID:28122138 62120 Ptma prothymosin alpha gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20190131 MGI PMID:28122138 62120 Ptma prothymosin alpha gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20190131 MGI PMID:28122138 62120 Ptma prothymosin alpha gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20190131 MGI PMID:28122138 62120 Ptma prothymosin alpha gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20190131 MGI PMID:28122138 62120 Ptma prothymosin alpha gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20190131 MGI PMID:28122138 62120 Ptma prothymosin alpha gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20190131 MGI PMID:28122138 62120 Ptma prothymosin alpha gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20190131 MGI PMID:28122138 62120 Ptma prothymosin alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62120 Ptma prothymosin alpha gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20190131 MGI PMID:28122138 62121 Kcnab3 potassium voltage-gated channel, shaker-related subfamily, beta member 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 62121 Kcnab3 potassium voltage-gated channel, shaker-related subfamily, beta member 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 62121 Kcnab3 potassium voltage-gated channel, shaker-related subfamily, beta member 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 62121 Kcnab3 potassium voltage-gated channel, shaker-related subfamily, beta member 3 gene MP:0001148 enlarged testis IEA N RGD:5509061 20210826 MGI 62121 Kcnab3 potassium voltage-gated channel, shaker-related subfamily, beta member 3 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20210826 MGI 62121 Kcnab3 potassium voltage-gated channel, shaker-related subfamily, beta member 3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 62121 Kcnab3 potassium voltage-gated channel, shaker-related subfamily, beta member 3 gene MP:0004882 enlarged lung IEA N RGD:5509061 20210826 MGI 62121 Kcnab3 potassium voltage-gated channel, shaker-related subfamily, beta member 3 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 62121 Kcnab3 potassium voltage-gated channel, shaker-related subfamily, beta member 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 62122 Treh trehalase (brush-border membrane glycoprotein) gene MP:0001666 abnormal intestinal absorption IEA N RGD:5509061 20111116 MGI 62122 Treh trehalase (brush-border membrane glycoprotein) gene MP:0002078 abnormal glucose homeostasis IEA N RGD:5509061 20111116 MGI 62122 Treh trehalase (brush-border membrane glycoprotein) gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 62124 Nrgn neurogranin gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20230119 MGI 62124 Nrgn neurogranin gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11016969 62124 Nrgn neurogranin gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11016969 62124 Nrgn neurogranin gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:12097504 62124 Nrgn neurogranin gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:11016969 62124 Nrgn neurogranin gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11016969 62124 Nrgn neurogranin gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:12097504 62124 Nrgn neurogranin gene MP:0002923 increased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:12097504 62124 Nrgn neurogranin gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20230119 MGI 62124 Nrgn neurogranin gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12097504 62124 Nrgn neurogranin gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20230119 MGI 62125 Fdft1 farnesyl diphosphate farnesyl transferase 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15793579 62125 Fdft1 farnesyl diphosphate farnesyl transferase 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:15793579 62125 Fdft1 farnesyl diphosphate farnesyl transferase 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:10521476 62125 Fdft1 farnesyl diphosphate farnesyl transferase 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15793579 62125 Fdft1 farnesyl diphosphate farnesyl transferase 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15793579 62125 Fdft1 farnesyl diphosphate farnesyl transferase 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:15793579 62125 Fdft1 farnesyl diphosphate farnesyl transferase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15793579 62125 Fdft1 farnesyl diphosphate farnesyl transferase 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15793579 62125 Fdft1 farnesyl diphosphate farnesyl transferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15793579 62125 Fdft1 farnesyl diphosphate farnesyl transferase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10521476 62125 Fdft1 farnesyl diphosphate farnesyl transferase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10521476 62125 Fdft1 farnesyl diphosphate farnesyl transferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62126 Fkbp1b FK506 binding protein 1b gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:11907581 62126 Fkbp1b FK506 binding protein 1b gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:11907581 62126 Fkbp1b FK506 binding protein 1b gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 62126 Fkbp1b FK506 binding protein 1b gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11907581 62126 Fkbp1b FK506 binding protein 1b gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:12837242 62126 Fkbp1b FK506 binding protein 1b gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12837242 62126 Fkbp1b FK506 binding protein 1b gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:11907581 62126 Fkbp1b FK506 binding protein 1b gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:18466757 62126 Fkbp1b FK506 binding protein 1b gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20231109 MGI PMID:11907581 62126 Fkbp1b FK506 binding protein 1b gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20231109 MGI PMID:11907581 62126 Fkbp1b FK506 binding protein 1b gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18466757 62126 Fkbp1b FK506 binding protein 1b gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11907581 62126 Fkbp1b FK506 binding protein 1b gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11907581 62126 Fkbp1b FK506 binding protein 1b gene MP:0008543 atrial fibrillation IAGP N RGD:5509061 20141003 MGI PMID:22828895 62126 Fkbp1b FK506 binding protein 1b gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:12837242 62126 Fkbp1b FK506 binding protein 1b gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201022 MGI 62126 Fkbp1b FK506 binding protein 1b gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:11907581 62126 Fkbp1b FK506 binding protein 1b gene MP:0021161 increased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:11907581 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20430974 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20181220 MGI PMID:28942122 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:11207362 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:11207362 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:20430974 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20181220 MGI PMID:28942122 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20201029 MGI PMID:30865697 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000119 abnormal tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:20430974 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:11207362 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20181220 MGI PMID:28942122 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20201029 MGI PMID:30865697 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20430974 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20181220 MGI PMID:28942122 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:11207362 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:11207362 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19661288 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:19661288 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:19661288 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:20430974 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:19661288 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001258 decreased body length IAGP N RGD:5509061 20201029 MGI PMID:30865697 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001260 increased body weight IAGP N RGD:5509061 20170803 MGI PMID:27746321 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20430974 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170803 MGI PMID:27746321 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11207362 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20181220 MGI PMID:28942122 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:11207362 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:20430974 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:19661288 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:11207362 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:20430974 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20430974 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20430974 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002083 premature death IAGP N RGD:5509061 20181220 MGI PMID:28942122 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002083 premature death IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:19661288 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:20430974 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:19661288 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:20430974 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:19661288 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:19661288 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:19661288 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:11207362 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:20430974 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20181220 MGI PMID:28942122 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:11207362 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20181220 MGI PMID:28942122 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:11207362 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0005060 accumulation of giant lysosomes in kidney/renal tubule cells IAGP N RGD:5509061 20141003 MGI PMID:19661288 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:20430974 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20160304 MGI PMID:11207362 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11207362 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:19661288 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0008583 absent photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0008733 abnormal hair shaft melanin granule distribution IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20201029 MGI PMID:30865697 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:19661288 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:20430974 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20170803 MGI PMID:27746321 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20181220 MGI PMID:28942122 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0010013 cerebral cortex pyramidal cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:20448277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0010014 hippocampus pyramidal cell degeneration IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20170803 MGI PMID:27746321 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20170803 MGI PMID:27746321 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20181220 MGI PMID:28942122 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20201029 MGI PMID:30865697 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20170803 MGI PMID:27746321 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20181220 MGI PMID:28942122 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20181220 MGI PMID:28942122 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11207362 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0011747 myelofibrosis IAGP N RGD:5509061 20141003 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0012007 abnormal chloride level IAGP N RGD:5509061 20190103 MGI PMID:24820037 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0013617 increased areal bone mineral density IAGP N RGD:5509061 20170803 MGI PMID:27746321 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0013617 increased areal bone mineral density IAGP N RGD:5509061 20220922 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20181220 MGI PMID:28942122 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20220922 MGI PMID:24185277 62127 Clcn7 chloride channel, voltage-sensitive 7 gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20190711 MGI PMID:19661288 62129 Tgm1 transglutaminase 1, K polypeptide gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:9448282 62129 Tgm1 transglutaminase 1, K polypeptide gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:9448282 62129 Tgm1 transglutaminase 1, K polypeptide gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:9448282 62129 Tgm1 transglutaminase 1, K polypeptide gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9448282 62129 Tgm1 transglutaminase 1, K polypeptide gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:9448282 62129 Tgm1 transglutaminase 1, K polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9448282 62129 Tgm1 transglutaminase 1, K polypeptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9448282 62129 Tgm1 transglutaminase 1, K polypeptide gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9448282 62129 Tgm1 transglutaminase 1, K polypeptide gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:9448282 62129 Tgm1 transglutaminase 1, K polypeptide gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9448282 62129 Tgm1 transglutaminase 1, K polypeptide gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:9448282 62129 Tgm1 transglutaminase 1, K polypeptide gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:11805136 62129 Tgm1 transglutaminase 1, K polypeptide gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:9448282 62129 Tgm1 transglutaminase 1, K polypeptide gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9448282 62130 Luzp1 leucine zipper protein 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0000923 abnormal roof plate morphology IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0011256 abnormal neural fold morphology IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18801334 62130 Luzp1 leucine zipper protein 1 gene MP:0012525 abnormal rhombic lip morphology IAGP N RGD:5509061 20141003 MGI PMID:18801334 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0000603 pale liver IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0001860 liver inflammation IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0002981 increased liver weight IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0003674 oxidative stress IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0003674 oxidative stress IAGP N RGD:5509061 20160929 MGI PMID:25977511 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20160929 MGI PMID:25977511 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20160929 MGI PMID:25977511 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20160929 MGI PMID:25977511 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20160929 MGI PMID:25977511 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0010042 abnormal oval cell physiology IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20160929 MGI PMID:25977511 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0010951 abnormal lipid oxidation IAGP N RGD:5509061 20160929 MGI PMID:25977511 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160929 MGI PMID:25977511 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20160929 MGI PMID:25977511 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20160929 MGI PMID:25977511 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20160929 MGI PMID:25977511 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0011638 abnormal mitochondrial chromosome morphology IAGP N RGD:5509061 20160505 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:25977511 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0014388 decreased hepatocyte mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:25977511 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:25448926 62137 Gfer growth factor, augmenter of liver regeneration gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:25448926 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12417724 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18339309 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:18339309 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12417724 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12417724 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:18339309 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12417724 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18339309 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12417724 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12417724 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12417724 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18339309 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12417724 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:18339309 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:12417724 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18339309 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18719666 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:12417724 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18339309 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12417724 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18339309 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18339309 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12417724 62139 Gpam glycerol-3-phosphate acyltransferase, mitochondrial gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18339309 62140 Psma5 proteasome subunit alpha 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210805 MGI PMID:34142127 62140 Psma5 proteasome subunit alpha 5 gene MP:0001393 ataxia IAGP N RGD:5509061 20210805 MGI PMID:34142127 62140 Psma5 proteasome subunit alpha 5 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20210805 MGI PMID:34142127 62140 Psma5 proteasome subunit alpha 5 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20210805 MGI PMID:34142127 62142 F10 coagulation factor X gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10739370 62142 F10 coagulation factor X gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18036190 62142 F10 coagulation factor X gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18036190 62142 F10 coagulation factor X gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18036190 62142 F10 coagulation factor X gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18036190 62142 F10 coagulation factor X gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 62142 F10 coagulation factor X gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20211021 MGI 62142 F10 coagulation factor X gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:18036190 62142 F10 coagulation factor X gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 62142 F10 coagulation factor X gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10739370 62142 F10 coagulation factor X gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10739370 62142 F10 coagulation factor X gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62142 F10 coagulation factor X gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10739370 62142 F10 coagulation factor X gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18036190 62142 F10 coagulation factor X gene MP:0020367 increased heart iron level IAGP N RGD:5509061 20161020 MGI PMID:18036190 62144 Gcm1 glial cells missing homolog 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22275534 62144 Gcm1 glial cells missing homolog 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10888880 62144 Gcm1 glial cells missing homolog 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:22275534 62144 Gcm1 glial cells missing homolog 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10713170 62144 Gcm1 glial cells missing homolog 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10713170 62144 Gcm1 glial cells missing homolog 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12049764 62144 Gcm1 glial cells missing homolog 1 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:10888880 62144 Gcm1 glial cells missing homolog 1 gene MP:0004560 abnormal chorionic plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10888880 62144 Gcm1 glial cells missing homolog 1 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20160804 MGI PMID:22275534 62144 Gcm1 glial cells missing homolog 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22275534 62144 Gcm1 glial cells missing homolog 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21765423 62144 Gcm1 glial cells missing homolog 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21765423 62144 Gcm1 glial cells missing homolog 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10888880 62144 Gcm1 glial cells missing homolog 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21765423 62144 Gcm1 glial cells missing homolog 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21765423 62144 Gcm1 glial cells missing homolog 1 gene MP:0011524 thick placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:22275534 62144 Gcm1 glial cells missing homolog 1 gene MP:0011526 abnormal placenta fetal blood space morphology IAGP N RGD:5509061 20141003 MGI PMID:22275534 62144 Gcm1 glial cells missing homolog 1 gene MP:0011529 increased placenta intervillous maternal lacunae size IAGP N RGD:5509061 20141003 MGI PMID:22275534 62144 Gcm1 glial cells missing homolog 1 gene MP:0011531 abnormal syncytiotrophoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:22275534 62144 Gcm1 glial cells missing homolog 1 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:22275534 62145 Gpc1 glypican 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 62145 Gpc1 glypican 1 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 62145 Gpc1 glypican 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 62145 Gpc1 glypican 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 62145 Gpc1 glypican 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 62145 Gpc1 glypican 1 gene MP:0000774 decreased brain size IEA N RGD:5509061 20210520 MGI 62145 Gpc1 glypican 1 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18064304 62145 Gpc1 glypican 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 62145 Gpc1 glypican 1 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210520 MGI 62145 Gpc1 glypican 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20151231 MGI PMID:19732411 62145 Gpc1 glypican 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 62145 Gpc1 glypican 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220519 MGI 62145 Gpc1 glypican 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18064304 62145 Gpc1 glypican 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210520 MGI 62146 Zranb2 zinc finger, RAN-binding domain containing 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 62146 Zranb2 zinc finger, RAN-binding domain containing 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20160804 MGI 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0000243 myoclonus IAGP N RGD:5509061 20160616 MGI PMID:26054439 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11331371 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15660664 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:21621520 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:21621520 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11331371 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15660664 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22812724 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:15660664 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:15660664 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0001400 hyperresponsive IAGP N RGD:5509061 20141003 MGI PMID:15660664 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15660664 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21621520 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20220421 MGI PMID:16807363 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0001443 poor grooming IAGP N RGD:5509061 20141003 MGI PMID:11331371 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15660664 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:15660664 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11331371 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0002064 seizures IAGP N RGD:5509061 20160616 MGI PMID:26054439 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20160616 MGI PMID:26054439 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15660664 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12466441 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16832820 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:21621520 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:10548105 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20160616 MGI PMID:26054439 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:11312285 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12466441 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15660664 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:22812724 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0003216 absence seizures IAGP N RGD:5509061 20160616 MGI PMID:26054439 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:15660664 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20160616 MGI PMID:26054439 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:16832820 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:11331371 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:10548105 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:22812724 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20160616 MGI PMID:26054439 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10548105 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11331371 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12466441 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21621520 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20160616 MGI PMID:26054439 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:23457547 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10816315 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10548105 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15660664 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11331371 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22812724 62147 Gabra1 gamma-aminobutyric acid type A receptor subunit alpha 1 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:26054439 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0001314 cornea opacity IEA N RGD:5509061 20200514 MGI 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20210128 MGI 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0001512 trunk curl IEA N RGD:5509061 20200514 MGI 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0001513 limb grasping IEA N RGD:5509061 20200514 MGI 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:21632935 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18313124 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:21632935 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20210128 MGI 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0002806 abnormal conditioned emotional response IAGP N RGD:5509061 20141003 MGI PMID:18313124 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210826 MGI 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:11021797 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:21632935 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210128 MGI 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210128 MGI 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18313124 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21632935 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20807777 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:20807777 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0009455 enhanced cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:20807777 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11021797 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16706856 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0009779 enhanced behavioral response to anesthetic IAGP N RGD:5509061 20141003 MGI PMID:20807777 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210826 MGI 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20221215 MGI 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210128 MGI 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20807777 62148 Gabra2 gamma-aminobutyric acid type A receptor subunit alpha 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 62149 Clic4 chloride intracellular channel 4 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19197003 62149 Clic4 chloride intracellular channel 4 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:22613027 62149 Clic4 chloride intracellular channel 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19197003 62149 Clic4 chloride intracellular channel 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21469130 62149 Clic4 chloride intracellular channel 4 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:22474389 62149 Clic4 chloride intracellular channel 4 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:19197003 62149 Clic4 chloride intracellular channel 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:22613027 62149 Clic4 chloride intracellular channel 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21469130 62149 Clic4 chloride intracellular channel 4 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19197003 62149 Clic4 chloride intracellular channel 4 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:22613027 62149 Clic4 chloride intracellular channel 4 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:19197003 62149 Clic4 chloride intracellular channel 4 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19197003 62149 Clic4 chloride intracellular channel 4 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19197003 62149 Clic4 chloride intracellular channel 4 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19197003 62149 Clic4 chloride intracellular channel 4 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:21469130 62149 Clic4 chloride intracellular channel 4 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21469130 62149 Clic4 chloride intracellular channel 4 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21469130 62149 Clic4 chloride intracellular channel 4 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:21469130 62149 Clic4 chloride intracellular channel 4 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21469130 62149 Clic4 chloride intracellular channel 4 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:21469130 62149 Clic4 chloride intracellular channel 4 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:21469130 62149 Clic4 chloride intracellular channel 4 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19197003 62149 Clic4 chloride intracellular channel 4 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:22613027 62149 Clic4 chloride intracellular channel 4 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21469130 62149 Clic4 chloride intracellular channel 4 gene MP:0012194 decreased keratinocyte migration IAGP N RGD:5509061 20141204 MGI PMID:22613027 62149 Clic4 chloride intracellular channel 4 gene MP:0014122 decreased pancreatic islet cell apoptosis IAGP N RGD:5509061 20170720 MGI PMID:25830089 62149 Clic4 chloride intracellular channel 4 gene MP:0020861 abnormal cornea wound healing IAGP N RGD:5509061 20181101 MGI PMID:22613027 62149 Clic4 chloride intracellular channel 4 gene MP:0030578 decreased keratinocyte adhesion IAGP N RGD:5509061 20180607 MGI PMID:22613027 62150 Grk4 G protein-coupled receptor kinase 4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:17021187 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220811 MGI 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20220811 MGI 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220811 MGI 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0000692 small spleen IEA N RGD:5509061 20220811 MGI 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220811 MGI 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220811 MGI 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220811 MGI 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0001147 small testis IEA N RGD:5509061 20220811 MGI 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12097508 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16597725 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16597725 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16597725 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021187 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12097508 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:16597725 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021187 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021187 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0004490 type IV spiral ligament fibrocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021187 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0004632 abnormal cochlear OHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17021187 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:17021187 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:17021187 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:12084936 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:15263904 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0009455 enhanced cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12084936 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12084936 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:17638582 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:17021187 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17021187 62151 Gabra5 gamma-aminobutyric acid type A receptor subunit alpha 5 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:15263904 62152 Gng7 guanine nucleotide binding protein (G protein), gamma 7 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19132103 62152 Gng7 guanine nucleotide binding protein (G protein), gamma 7 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19132103 62152 Gng7 guanine nucleotide binding protein (G protein), gamma 7 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:12488442 62152 Gng7 guanine nucleotide binding protein (G protein), gamma 7 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:19132103 62152 Gng7 guanine nucleotide binding protein (G protein), gamma 7 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:22207761 62152 Gng7 guanine nucleotide binding protein (G protein), gamma 7 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20111116 MGI 62152 Gng7 guanine nucleotide binding protein (G protein), gamma 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22207761 62152 Gng7 guanine nucleotide binding protein (G protein), gamma 7 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:19132103 62152 Gng7 guanine nucleotide binding protein (G protein), gamma 7 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19132103 62152 Gng7 guanine nucleotide binding protein (G protein), gamma 7 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12488442 62152 Gng7 guanine nucleotide binding protein (G protein), gamma 7 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:22207761 62152 Gng7 guanine nucleotide binding protein (G protein), gamma 7 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:22207761 62152 Gng7 guanine nucleotide binding protein (G protein), gamma 7 gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19132103 62152 Gng7 guanine nucleotide binding protein (G protein), gamma 7 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:22207761 62152 Gng7 guanine nucleotide binding protein (G protein), gamma 7 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20151217 MGI PMID:24496082 62153 Gabra6 gamma-aminobutyric acid type A receptor subunit alpha 6 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:22252133 62153 Gabra6 gamma-aminobutyric acid type A receptor subunit alpha 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12820171 62153 Gabra6 gamma-aminobutyric acid type A receptor subunit alpha 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17693261 62153 Gabra6 gamma-aminobutyric acid type A receptor subunit alpha 6 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:22252133 62153 Gabra6 gamma-aminobutyric acid type A receptor subunit alpha 6 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22252133 62153 Gabra6 gamma-aminobutyric acid type A receptor subunit alpha 6 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:22252133 62153 Gabra6 gamma-aminobutyric acid type A receptor subunit alpha 6 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22252133 62153 Gabra6 gamma-aminobutyric acid type A receptor subunit alpha 6 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:22252133 62153 Gabra6 gamma-aminobutyric acid type A receptor subunit alpha 6 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:9106623 62153 Gabra6 gamma-aminobutyric acid type A receptor subunit alpha 6 gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20141003 MGI PMID:22252133 62153 Gabra6 gamma-aminobutyric acid type A receptor subunit alpha 6 gene MP:0011039 abnormal vestibuloocular dark reflex IAGP N RGD:5509061 20141003 MGI PMID:22252133 62153 Gabra6 gamma-aminobutyric acid type A receptor subunit alpha 6 gene MP:0011040 abnormal vestibuloocular light reflex IAGP N RGD:5509061 20141003 MGI PMID:22252133 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12848940 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:16042312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:7502080 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:16042312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16914668 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15541312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10195181 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8938126 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12848940 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8938126 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16099814 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16216087 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20240627 MGI PMID:16099814 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:16099814 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001401 jumpy IAGP N RGD:5509061 20141003 MGI PMID:7502080 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12848940 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16042312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16042312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16216087 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:8938126 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:16216087 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:8938126 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001440 abnormal grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:7502080 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:8938126 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001460 abnormal olfactory discrimination memory IAGP N RGD:5509061 20141003 MGI PMID:16216087 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16216087 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10195181 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7502080 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:12848940 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:16543133 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:15541312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:15797551 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:8938126 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:15541312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:16216087 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20151119 MGI PMID:20927382 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10195181 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16914668 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:7502080 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:10195181 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12848940 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10195181 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16042312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10894545 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:9811877 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:16099814 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:7502080 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:15541312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:10195181 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16042312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16099814 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16914668 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:7502080 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:18701074 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16914668 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:10195181 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:12848940 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:16914668 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002918 abnormal paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:16914668 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12848940 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:8938126 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20151119 MGI PMID:20927382 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:16914668 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:16042312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:8938126 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:16099814 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:7502080 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16914668 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:16042312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:12848940 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:10195181 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0005407 hyperalgesia IAGP N RGD:5509061 20141003 MGI PMID:15541312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7502080 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:16042312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:10195181 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:16914668 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:16914668 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20151119 MGI PMID:20927382 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0008532 decreased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:15541312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:7502080 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20151119 MGI PMID:20927382 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16914668 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16042312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20211021 MGI 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0011002 enhanced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15541312 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10195181 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7502080 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10894545 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12848940 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8938126 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20151119 MGI PMID:20927382 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0020478 abnormal circadian sleep/wake cycle IEA N RGD:5509061 20171012 MGI 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:7502080 62154 Gria2 glutamate receptor, ionotropic, AMPA2 (alpha 2) gene MP:0031650 decreased mounting behavior IAGP N RGD:5509061 20240905 MGI PMID:16099814 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0000950 abnormal seizure response to pharmacological agent IEA N RGD:5509061 20111116 MGI 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20662939 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:20662939 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20662939 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18316356 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17296559 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:17296559 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:20662939 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17296559 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:20662939 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:17296559 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:17296559 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:20662939 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17296559 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:24349437 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0002911 abnormal inhibitory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:17296559 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:17296559 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:15800200 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:18316356 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:17296559 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:24349437 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:17296559 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:20662939 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:17296559 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20170202 MGI PMID:25010494 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20662939 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20662939 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:20662939 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20662939 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0014369 enhanced spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:20662939 62155 Gria4 glutamate receptor, ionotropic, AMPA4 (alpha 4) gene MP:0031391 increased locomotor activity IEA N RGD:5509061 20220421 MGI 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12861009 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12861009 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0001142 abnormal vagina orifice morphology IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20220714 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12861009 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:12861009 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12861009 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12861009 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19121371 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12861009 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:12861009 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:12861009 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:17272395 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0004909 increased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:12861009 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:12861009 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0005137 increased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:17272395 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0005180 abnormal circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12861009 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12861009 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0008459 abnormal circulating pancreatic peptide level IAGP N RGD:5509061 20141003 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0008459 abnormal circulating pancreatic peptide level IAGP N RGD:5509061 20141003 MGI PMID:12861009 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12861009 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0010143 enhanced fertility IAGP N RGD:5509061 20220714 MGI PMID:12000791 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17272395 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:16364461 62156 Npy4r neuropeptide Y receptor Y4 gene MP:0030603 increased sperm number IAGP N RGD:5509061 20220714 MGI PMID:12000791 62157 Lbp lipopolysaccharide binding protein gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:11884468 62157 Lbp lipopolysaccharide binding protein gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9338787 62157 Lbp lipopolysaccharide binding protein gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:16493079 62157 Lbp lipopolysaccharide binding protein gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16493079 62157 Lbp lipopolysaccharide binding protein gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:16493079 62157 Lbp lipopolysaccharide binding protein gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:9396775 62157 Lbp lipopolysaccharide binding protein gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11160257 62157 Lbp lipopolysaccharide binding protein gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 62157 Lbp lipopolysaccharide binding protein gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:11884468 62157 Lbp lipopolysaccharide binding protein gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11160257 62157 Lbp lipopolysaccharide binding protein gene MP:0008556 abnormal tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16493079 62157 Lbp lipopolysaccharide binding protein gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:9396775 62157 Lbp lipopolysaccharide binding protein gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:16493079 62157 Lbp lipopolysaccharide binding protein gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9396775 62157 Lbp lipopolysaccharide binding protein gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 62157 Lbp lipopolysaccharide binding protein gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20221110 MGI PMID:34370553 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20161103 MGI PMID:27053112 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20161103 MGI PMID:27053112 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20161103 MGI PMID:27053112 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20221110 MGI PMID:34370553 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20221110 MGI PMID:34370553 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20221110 MGI PMID:34370553 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20160804 MGI 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20160804 MGI 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20161103 MGI PMID:27053112 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20161103 MGI PMID:27053112 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20161103 MGI PMID:27053112 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20141003 MGI 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20141003 MGI 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0009441 delayed skin barrier formation IAGP N RGD:5509061 20161103 MGI PMID:27053112 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20221110 MGI PMID:34370553 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20161103 MGI PMID:27053112 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20221110 MGI PMID:34370553 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20221110 MGI PMID:34370553 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20161103 MGI PMID:27053112 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20161103 MGI PMID:27053112 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0020016 decreased aldehyde dehydrogenase activity IAGP N RGD:5509061 20161103 MGI PMID:27053112 62158 Aldh3a2 aldehyde dehydrogenase family 3, subfamily A2 gene MP:0020583 decreased ceramide level IAGP N RGD:5509061 20221110 MGI PMID:34370553 62159 Casp9 caspase 9 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:9708735 62159 Casp9 caspase 9 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9708735 62159 Casp9 caspase 9 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15156583 62159 Casp9 caspase 9 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9708735 62159 Casp9 caspase 9 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9708735 62159 Casp9 caspase 9 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:15210727 62159 Casp9 caspase 9 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:9708735 62159 Casp9 caspase 9 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11150333 62159 Casp9 caspase 9 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9708735 62159 Casp9 caspase 9 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:11150333 62159 Casp9 caspase 9 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:9708735 62159 Casp9 caspase 9 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11062535 62159 Casp9 caspase 9 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11150333 62159 Casp9 caspase 9 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12107826 62159 Casp9 caspase 9 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15156583 62159 Casp9 caspase 9 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15210727 62159 Casp9 caspase 9 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15156583 62159 Casp9 caspase 9 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15210727 62159 Casp9 caspase 9 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11150333 62159 Casp9 caspase 9 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15156583 62159 Casp9 caspase 9 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9708735 62159 Casp9 caspase 9 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:9708735 62159 Casp9 caspase 9 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:9708735 62159 Casp9 caspase 9 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11150333 62159 Casp9 caspase 9 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11150333 62159 Casp9 caspase 9 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15210727 62159 Casp9 caspase 9 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15156583 62159 Casp9 caspase 9 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0009258 abnormal thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9708735 62159 Casp9 caspase 9 gene MP:0009258 abnormal thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0009340 abnormal splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9708735 62159 Casp9 caspase 9 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9708736 62159 Casp9 caspase 9 gene MP:0012091 increased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:9708735 62159 Casp9 caspase 9 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:9708735 62159 Casp9 caspase 9 gene MP:0012540 abnormal lamina terminalis morphology IAGP N RGD:5509061 20141003 MGI PMID:9708735 62159 Casp9 caspase 9 gene MP:0013228 brain ventricle stenosis IAGP N RGD:5509061 20161103 MGI PMID:9708735 62160 Dpf1 double PHD fingers 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 62160 Dpf1 double PHD fingers 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20230601 MGI 62160 Dpf1 double PHD fingers 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 62161 Grb14 growth factor receptor bound protein 14 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14749734 62161 Grb14 growth factor receptor bound protein 14 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:14749734 62161 Grb14 growth factor receptor bound protein 14 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:14749734 62161 Grb14 growth factor receptor bound protein 14 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:14749734 62161 Grb14 growth factor receptor bound protein 14 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:14749734 62161 Grb14 growth factor receptor bound protein 14 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:14749734 62162 Ramp1 receptor (calcitonin) activity modifying protein 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 62162 Ramp1 receptor (calcitonin) activity modifying protein 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17923674 62162 Ramp1 receptor (calcitonin) activity modifying protein 1 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:17923674 62162 Ramp1 receptor (calcitonin) activity modifying protein 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17923674 62162 Ramp1 receptor (calcitonin) activity modifying protein 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17923674 62162 Ramp1 receptor (calcitonin) activity modifying protein 1 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:17923674 62162 Ramp1 receptor (calcitonin) activity modifying protein 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:17923674 62162 Ramp1 receptor (calcitonin) activity modifying protein 1 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17923674 62162 Ramp1 receptor (calcitonin) activity modifying protein 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160421 MGI 62163 Rhag Rhesus blood group-associated A glycoprotein gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 62163 Rhag Rhesus blood group-associated A glycoprotein gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 62163 Rhag Rhesus blood group-associated A glycoprotein gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 62163 Rhag Rhesus blood group-associated A glycoprotein gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 62163 Rhag Rhesus blood group-associated A glycoprotein gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 62163 Rhag Rhesus blood group-associated A glycoprotein gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 62163 Rhag Rhesus blood group-associated A glycoprotein gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 62163 Rhag Rhesus blood group-associated A glycoprotein gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 62163 Rhag Rhesus blood group-associated A glycoprotein gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 62163 Rhag Rhesus blood group-associated A glycoprotein gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19807729 62163 Rhag Rhesus blood group-associated A glycoprotein gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 62163 Rhag Rhesus blood group-associated A glycoprotein gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 62163 Rhag Rhesus blood group-associated A glycoprotein gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20230601 MGI 62163 Rhag Rhesus blood group-associated A glycoprotein gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:19807729 62163 Rhag Rhesus blood group-associated A glycoprotein gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19807729 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18097473 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:18097473 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18097473 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:18097473 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:18097475 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18097475 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17470425 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:18097475 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:18097473 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0002450 abnormal lymph organ development IAGP N RGD:5509061 20141003 MGI PMID:18097475 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:18097473 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0003230 abnormal umbilical artery morphology IAGP N RGD:5509061 20141003 MGI PMID:18097473 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0003390 lymphedema IAGP N RGD:5509061 20141003 MGI PMID:18097475 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18097473 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18097473 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18097475 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:18097473 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18097473 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18097473 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:18097475 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0010664 abnormal vitelline artery morphology IAGP N RGD:5509061 20141003 MGI PMID:18097473 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17470425 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18097473 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18097475 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0011514 skin hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18097473 62164 Ramp2 receptor (calcitonin) activity modifying protein 2 gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:18097473 62165 Ramp3 receptor (calcitonin) activity modifying protein 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17470425 62172 Vamp3 vesicle-associated membrane protein 3 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20181227 MGI 62172 Vamp3 vesicle-associated membrane protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11238894 62172 Vamp3 vesicle-associated membrane protein 3 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:16793874 62172 Vamp3 vesicle-associated membrane protein 3 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:17065550 62172 Vamp3 vesicle-associated membrane protein 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 62172 Vamp3 vesicle-associated membrane protein 3 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:16793874 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0000046 abnormal sulcus ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:11784868 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:15456880 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:11784868 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11784868 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11784868 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:13129926 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:13129926 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0002174 abnormal gastrulation movements IAGP N RGD:5509061 20141003 MGI PMID:13129926 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:11784868 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:15456880 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15456880 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15456880 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:15456880 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:15456880 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:20566846 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:13129926 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:15456880 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11784868 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20210708 MGI PMID:32868928 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:11784868 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:20566846 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:15456880 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20210708 MGI PMID:32868928 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:15456880 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17515897 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:13129926 62174 Nr4a3 nuclear receptor subfamily 4, group A, member 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:13129926 62175 Ghrh growth hormone releasing hormone gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20181227 MGI 62175 Ghrh growth hormone releasing hormone gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:15155578 62175 Ghrh growth hormone releasing hormone gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:15155578 62175 Ghrh growth hormone releasing hormone gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15155578 62175 Ghrh growth hormone releasing hormone gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15155578 62175 Ghrh growth hormone releasing hormone gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15155578 62175 Ghrh growth hormone releasing hormone gene MP:0002659 pituitary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15155578 62175 Ghrh growth hormone releasing hormone gene MP:0002834 decreased heart weight IEA N RGD:5509061 20201022 MGI 62175 Ghrh growth hormone releasing hormone gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20181227 MGI 62175 Ghrh growth hormone releasing hormone gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 62175 Ghrh growth hormone releasing hormone gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:15155578 62175 Ghrh growth hormone releasing hormone gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21846799 62175 Ghrh growth hormone releasing hormone gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:15155578 62175 Ghrh growth hormone releasing hormone gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 62175 Ghrh growth hormone releasing hormone gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20181227 MGI 62175 Ghrh growth hormone releasing hormone gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 62175 Ghrh growth hormone releasing hormone gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 62175 Ghrh growth hormone releasing hormone gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 62176 Clns1a chloride channel, nucleotide-sensitive, 1A gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:10777517 62176 Clns1a chloride channel, nucleotide-sensitive, 1A gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10777517 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15947421 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20220519 MGI 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0001259 abnormal body weight IEA N RGD:5509061 20240523 MGI 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15979591 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20230601 MGI 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10827176 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:15979591 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0003604 single kidney IEA N RGD:5509061 20220519 MGI 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:10827176 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:10827175 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0008173 increased follicular B cell number IEA N RGD:5509061 20220519 MGI 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:15979591 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0011940 decreased food intake IEA N RGD:5509061 20230601 MGI 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210520 MGI 62178 Timp2 tissue inhibitor of metalloproteinase 2 gene MP:0012320 abnormal body fat mass IEA N RGD:5509061 20240523 MGI 62179 Avpr1b arginine vasopressin receptor 1B gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:12399951 62179 Avpr1b arginine vasopressin receptor 1B gene MP:0002664 decreased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:14722621 62179 Avpr1b arginine vasopressin receptor 1B gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:14722621 62179 Avpr1b arginine vasopressin receptor 1B gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:14722621 62179 Avpr1b arginine vasopressin receptor 1B gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:12399951 62179 Avpr1b arginine vasopressin receptor 1B gene MP:0002906 increased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20111116 MGI 62179 Avpr1b arginine vasopressin receptor 1B gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:12399951 62180 Pdcd2 programmed cell death 2 gene MP:0001340 abnormal eyelid morphology IEA N RGD:5509061 20160421 MGI 62180 Pdcd2 programmed cell death 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:20813103 62180 Pdcd2 programmed cell death 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150122 MGI PMID:25150276 62180 Pdcd2 programmed cell death 2 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:20813103 62180 Pdcd2 programmed cell death 2 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:20813103 62180 Pdcd2 programmed cell death 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20813103 62180 Pdcd2 programmed cell death 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20813103 62180 Pdcd2 programmed cell death 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62180 Pdcd2 programmed cell death 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 62180 Pdcd2 programmed cell death 2 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20150910 MGI PMID:18952847 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20181129 MGI PMID:17419998 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20150910 MGI PMID:18952847 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21514245 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:21514245 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17419998 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:17419998 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:17419998 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0001215 skin hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17419998 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17419998 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17419998 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20150910 MGI PMID:18952847 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:17419998 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20160804 MGI 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20220203 MGI PMID:21527500 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220203 MGI PMID:21527500 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220203 MGI PMID:21527500 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21514245 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12832465 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:17419998 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20150910 MGI PMID:18952847 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20150910 MGI PMID:18952847 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:17419998 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20220203 MGI PMID:21527500 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20220203 MGI PMID:21527500 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:23945236 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21514245 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17419998 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0009819 abnormal circulating androgen level IAGP N RGD:5509061 20220203 MGI PMID:21527500 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0009905 absent tongue IAGP N RGD:5509061 20150910 MGI PMID:18952847 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17419998 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0010283 decreased classified tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21514245 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17419998 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20220203 MGI PMID:21527500 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0014269 decreased testes secretion IAGP N RGD:5509061 20230810 MGI PMID:21527500 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0030575 decreased hair follicle cell proliferation IAGP N RGD:5509061 20181129 MGI PMID:17419998 62181 Map2k2 mitogen-activated protein kinase kinase 2 gene MP:0031436 decreased copulatory plug deposition IAGP N RGD:5509061 20220922 MGI PMID:21527500 62182 Mefv Mediterranean fever gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12667444 62182 Mefv Mediterranean fever gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12667444 62182 Mefv Mediterranean fever gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0002933 joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008654 increased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:23226472 62182 Mefv Mediterranean fever gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008684 increased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:23226472 62182 Mefv Mediterranean fever gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008697 decreased interleukin-3 secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008711 increased interleukin-9 secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 62182 Mefv Mediterranean fever gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12667444 62182 Mefv Mediterranean fever gene MP:0011081 decreased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12667444 62182 Mefv Mediterranean fever gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21600797 62183 Map2k5 mitogen-activated protein kinase kinase 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15601854 62183 Map2k5 mitogen-activated protein kinase kinase 5 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:15601854 62183 Map2k5 mitogen-activated protein kinase kinase 5 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:15601854 62183 Map2k5 mitogen-activated protein kinase kinase 5 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15601854 62183 Map2k5 mitogen-activated protein kinase kinase 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15601854 62183 Map2k5 mitogen-activated protein kinase kinase 5 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15601854 62183 Map2k5 mitogen-activated protein kinase kinase 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15601854 62183 Map2k5 mitogen-activated protein kinase kinase 5 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:15601854 62183 Map2k5 mitogen-activated protein kinase kinase 5 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15601854 62183 Map2k5 mitogen-activated protein kinase kinase 5 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:15601854 62183 Map2k5 mitogen-activated protein kinase kinase 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15601854 62184 Tas1r1 taste receptor, type 1, member 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22427794 62184 Tas1r1 taste receptor, type 1, member 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:22427794 62184 Tas1r1 taste receptor, type 1, member 1 gene MP:0004213 abnormal umami taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:14636554 62184 Tas1r1 taste receptor, type 1, member 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:22427794 62184 Tas1r1 taste receptor, type 1, member 1 gene MP:0005423 abnormal somatic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:14636554 62184 Tas1r1 taste receptor, type 1, member 1 gene MP:0013288 premature acrosome reaction IAGP N RGD:5509061 20191226 MGI PMID:22427794 62184 Tas1r1 taste receptor, type 1, member 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:22427794 62184 Tas1r1 taste receptor, type 1, member 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:22427794 62185 Eci1 enoyl-Coenzyme A delta isomerase 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:11916962 62185 Eci1 enoyl-Coenzyme A delta isomerase 1 gene MP:0005283 increased unsaturated fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:11916962 62185 Eci1 enoyl-Coenzyme A delta isomerase 1 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11916962 62185 Eci1 enoyl-Coenzyme A delta isomerase 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11916962 62187 Tas1r2 taste receptor, type 1, member 2 gene MP:0004209 abnormal sweet taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:14636554 62187 Tas1r2 taste receptor, type 1, member 2 gene MP:0004209 abnormal sweet taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20965149 62187 Tas1r2 taste receptor, type 1, member 2 gene MP:0005423 abnormal somatic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:14636554 62188 Dcn decorin gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12102052 62188 Dcn decorin gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:11891213 62188 Dcn decorin gene MP:0000619 salivary gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10077642 62188 Dcn decorin gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10077642 62188 Dcn decorin gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:10077642 62188 Dcn decorin gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:9024701 62188 Dcn decorin gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:12102052 62188 Dcn decorin gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:9024701 62188 Dcn decorin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21502335 62188 Dcn decorin gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:15331421 62188 Dcn decorin gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:21502335 62188 Dcn decorin gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21502335 62188 Dcn decorin gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21502335 62188 Dcn decorin gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10077642 62188 Dcn decorin gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10077642 62188 Dcn decorin gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10077642 62188 Dcn decorin gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:21502335 62188 Dcn decorin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10077642 62188 Dcn decorin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150917 MGI PMID:26029887 62188 Dcn decorin gene MP:0002294 short gestation period IAGP N RGD:5509061 20141003 MGI PMID:21502335 62188 Dcn decorin gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11285303 62188 Dcn decorin gene MP:0002704 tubular nephritis IAGP N RGD:5509061 20141003 MGI PMID:11891213 62188 Dcn decorin gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:11891213 62188 Dcn decorin gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:12102052 62188 Dcn decorin gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:9024701 62188 Dcn decorin gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11891213 62188 Dcn decorin gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10077642 62188 Dcn decorin gene MP:0003668 abnormal periodontal ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:11140699 62188 Dcn decorin gene MP:0003669 periodontal ligament hypercellularity IAGP N RGD:5509061 20141003 MGI PMID:11140699 62188 Dcn decorin gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:12102052 62188 Dcn decorin gene MP:0004126 thin hypodermis IAGP N RGD:5509061 20141003 MGI PMID:12102052 62188 Dcn decorin gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11891213 62188 Dcn decorin gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:12102052 62188 Dcn decorin gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:11891213 62188 Dcn decorin gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:9024701 62188 Dcn decorin gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:12102052 62188 Dcn decorin gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:9024701 62188 Dcn decorin gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:12102052 62188 Dcn decorin gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:12102052 62188 Dcn decorin gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:9024701 62188 Dcn decorin gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11891213 62188 Dcn decorin gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10077642 62188 Dcn decorin gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:12102052 62188 Dcn decorin gene MP:0010962 decreased compact bone mass IAGP N RGD:5509061 20141003 MGI PMID:12102052 62188 Dcn decorin gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:11891213 62188 Dcn decorin gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:15277214 62188 Dcn decorin gene MP:0011642 abnormal bone collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:12102052 62188 Dcn decorin gene MP:0012008 delayed parturition IAGP N RGD:5509061 20141003 MGI PMID:21502335 62188 Dcn decorin gene MP:0012009 early parturition IAGP N RGD:5509061 20141003 MGI PMID:21502335 62188 Dcn decorin gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:10077642 62189 Nme6 NME/NM23 nucleoside diphosphate kinase 6 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 62189 Nme6 NME/NM23 nucleoside diphosphate kinase 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62189 Nme6 NME/NM23 nucleoside diphosphate kinase 6 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 62190 Ptafr platelet-activating factor receptor gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:14742561 62190 Ptafr platelet-activating factor receptor gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:14767826 62190 Ptafr platelet-activating factor receptor gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16299272 62190 Ptafr platelet-activating factor receptor gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 62190 Ptafr platelet-activating factor receptor gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:14742561 62190 Ptafr platelet-activating factor receptor gene MP:0005167 abnormal blood-brain barrier function IAGP N RGD:5509061 20141003 MGI PMID:16299272 62190 Ptafr platelet-activating factor receptor gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:9607919 62191 Maoa monoamine oxidase A gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10844034 62191 Maoa monoamine oxidase A gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:15272015 62191 Maoa monoamine oxidase A gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:18418249 62191 Maoa monoamine oxidase A gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0001357 increased aggression towards humans IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15272015 62191 Maoa monoamine oxidase A gene MP:0001400 hyperresponsive IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18418249 62191 Maoa monoamine oxidase A gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:15272015 62191 Maoa monoamine oxidase A gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0001440 abnormal grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:15272015 62191 Maoa monoamine oxidase A gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10844034 62191 Maoa monoamine oxidase A gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:19910579 62191 Maoa monoamine oxidase A gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:19910579 62191 Maoa monoamine oxidase A gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:19910579 62191 Maoa monoamine oxidase A gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:16112493 62191 Maoa monoamine oxidase A gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:10844034 62191 Maoa monoamine oxidase A gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:15272015 62191 Maoa monoamine oxidase A gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:7792602 62191 Maoa monoamine oxidase A gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20180920 MGI PMID:15272015 62191 Maoa monoamine oxidase A gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20180920 MGI PMID:7792602 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20170105 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20170105 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15258586 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0001987 alcohol preference IAGP N RGD:5509061 20141003 MGI PMID:15258586 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20170105 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20230601 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15258586 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:15258586 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20180503 MGI PMID:28169986 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20211021 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20170105 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0004685 calcified intervertebral disk IAGP N RGD:5509061 20181129 MGI PMID:27237608 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20181129 MGI PMID:27237608 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15258586 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20180503 MGI PMID:28169986 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20180503 MGI PMID:23603835 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180503 MGI PMID:28169986 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20190502 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20181227 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20181129 MGI PMID:27237608 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20180503 MGI PMID:28169986 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:15258586 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20170105 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20170105 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20181129 MGI PMID:27237608 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20181129 MGI PMID:27237608 62192 Slc29a1 solute carrier family 29 (nucleoside transporters), member 1 gene MP:0030222 hyperostosis IAGP N RGD:5509061 20181129 MGI PMID:27237608 62193 Gabrr1 gamma-aminobutyric acid type A receptor subunit rho 1 gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:17923325 62193 Gabrr1 gamma-aminobutyric acid type A receptor subunit rho 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12970343 62193 Gabrr1 gamma-aminobutyric acid type A receptor subunit rho 1 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:12970343 62193 Gabrr1 gamma-aminobutyric acid type A receptor subunit rho 1 gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:12970343 62193 Gabrr1 gamma-aminobutyric acid type A receptor subunit rho 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12019334 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18667149 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10536021 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:18667149 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:18667149 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:18667149 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:18667149 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15897254 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15897254 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10536021 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10536021 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:24027099 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18667149 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:18667149 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:24027099 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:24027099 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:10536021 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:24027099 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:10536021 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:18667149 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0009778 impaired behavioral response to anesthetic IAGP N RGD:5509061 20141003 MGI PMID:10536021 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:24027099 62194 Gabrd gamma-aminobutyric acid (GABA) A receptor, subunit delta gene MP:0011987 abnormal GABAergic neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:24027099 62195 Gabrr2 gamma-aminobutyric acid type A receptor subunit rho 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 62195 Gabrr2 gamma-aminobutyric acid type A receptor subunit rho 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 62195 Gabrr2 gamma-aminobutyric acid type A receptor subunit rho 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170105 MGI 62195 Gabrr2 gamma-aminobutyric acid type A receptor subunit rho 2 gene MP:0001147 small testis IEA N RGD:5509061 20170105 MGI 62196 Gpr182 G protein-coupled receptor 182 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20190502 MGI 62196 Gpr182 G protein-coupled receptor 182 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20210610 MGI PMID:33875597 62196 Gpr182 G protein-coupled receptor 182 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20210610 MGI PMID:33875597 62196 Gpr182 G protein-coupled receptor 182 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 62196 Gpr182 G protein-coupled receptor 182 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20210610 MGI PMID:33875597 62196 Gpr182 G protein-coupled receptor 182 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 62196 Gpr182 G protein-coupled receptor 182 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20210610 MGI PMID:33875597 62196 Gpr182 G protein-coupled receptor 182 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 62196 Gpr182 G protein-coupled receptor 182 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 62196 Gpr182 G protein-coupled receptor 182 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20210610 MGI PMID:33875597 62196 Gpr182 G protein-coupled receptor 182 gene MP:0031220 increased circulating CXCL10 level IAGP N RGD:5509061 20210610 MGI PMID:33875597 62197 Ptprn2 protein tyrosine phosphatase receptor type N polypeptide 2 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20220120 MGI PMID:16269463 62197 Ptprn2 protein tyrosine phosphatase receptor type N polypeptide 2 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20220120 MGI PMID:16269463 62197 Ptprn2 protein tyrosine phosphatase receptor type N polypeptide 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20220120 MGI PMID:16269463 62197 Ptprn2 protein tyrosine phosphatase receptor type N polypeptide 2 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20220120 MGI PMID:16269463 62197 Ptprn2 protein tyrosine phosphatase receptor type N polypeptide 2 gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20220120 MGI PMID:16269463 62197 Ptprn2 protein tyrosine phosphatase receptor type N polypeptide 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220120 MGI PMID:16269463 62197 Ptprn2 protein tyrosine phosphatase receptor type N polypeptide 2 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20220120 MGI PMID:16269463 62197 Ptprn2 protein tyrosine phosphatase receptor type N polypeptide 2 gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20220120 MGI PMID:16269463 62197 Ptprn2 protein tyrosine phosphatase receptor type N polypeptide 2 gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20220120 MGI PMID:16269463 62197 Ptprn2 protein tyrosine phosphatase receptor type N polypeptide 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15220191 62198 Psmc3 proteasome (prosome, macropain) 26S subunit, ATPase 3 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:10945464 62198 Psmc3 proteasome (prosome, macropain) 26S subunit, ATPase 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10945464 62198 Psmc3 proteasome (prosome, macropain) 26S subunit, ATPase 3 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10945464 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17166844 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:17166844 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20191031 MGI PMID:31371497 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17166844 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17166844 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:17341595 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20190207 MGI PMID:27335465 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:11851872 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20191031 MGI PMID:31371497 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20191031 MGI PMID:31371497 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:20133709 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20190207 MGI PMID:27335465 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20190207 MGI PMID:27335465 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17341595 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20190207 MGI PMID:27335465 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19996385 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18160655 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20190207 MGI PMID:27335465 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19996385 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11238557 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17341595 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12524534 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:12193651 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20141003 MGI PMID:17341595 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:17341595 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17341595 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14993927 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17341595 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20141003 MGI PMID:17166844 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20141003 MGI PMID:11238557 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20141003 MGI PMID:19996385 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:17341595 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:17563384 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20191031 MGI PMID:31371497 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17166844 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17166844 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20190207 MGI PMID:27335465 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17341595 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19996385 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19996385 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20191031 MGI PMID:31371497 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20191031 MGI PMID:31371497 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20191031 MGI PMID:31371497 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:17166844 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20191031 MGI PMID:31371497 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:17166844 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0008717 increased lung squamous cell carcinoma incidence IAGP N RGD:5509061 20190207 MGI PMID:27335465 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0009229 abnormal neurohypophysis median eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12193651 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20141003 MGI PMID:17166844 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0009688 abnormal spinal cord central canal morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12524534 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20191031 MGI PMID:31371497 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10968783 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20190207 MGI PMID:27335465 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20190207 MGI PMID:27335465 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0010901 abnormal pulmonary alveolar parenchyma morphology IAGP N RGD:5509061 20190207 MGI PMID:27335465 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0013218 abnormal substantia nigra pars reticulata morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0013598 Leydig cell hypertrophy IAGP N RGD:5509061 20150319 MGI PMID:17341595 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0013908 small lateral ventricles IAGP N RGD:5509061 20161103 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0013909 small third ventricle IAGP N RGD:5509061 20161103 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0013910 small fourth ventricle IAGP N RGD:5509061 20161103 MGI PMID:12368482 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:17341595 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20191031 MGI PMID:31371497 62199 Nr1h2 nuclear receptor subfamily 1, group H, member 2 gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:19996385 62200 Rps7 ribosomal protein S7 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:15384171 62200 Rps7 ribosomal protein S7 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15384171 62200 Rps7 ribosomal protein S7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:15384171 62200 Rps7 ribosomal protein S7 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0004600 abnormal vertebral transverse process morphology IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0004645 decreased vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0009843 decreased neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:15384171 62200 Rps7 ribosomal protein S7 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0012533 uveal coloboma IAGP N RGD:5509061 20141003 MGI PMID:23382688 62200 Rps7 ribosomal protein S7 gene MP:0012536 delayed optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:23382688 62201 Rab7 RAB7, member RAS oncogene family gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20240425 MGI PMID:37878717 62201 Rab7 RAB7, member RAS oncogene family gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:22990867 62201 Rab7 RAB7, member RAS oncogene family gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 62201 Rab7 RAB7, member RAS oncogene family gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20160728 MGI PMID:23615463 62201 Rab7 RAB7, member RAS oncogene family gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20240425 MGI PMID:37878717 62201 Rab7 RAB7, member RAS oncogene family gene MP:0003674 oxidative stress IAGP N RGD:5509061 20160728 MGI PMID:23615463 62201 Rab7 RAB7, member RAS oncogene family gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20160728 MGI PMID:23615463 62201 Rab7 RAB7, member RAS oncogene family gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20160728 MGI PMID:23615463 62201 Rab7 RAB7, member RAS oncogene family gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20240425 MGI PMID:37878717 62201 Rab7 RAB7, member RAS oncogene family gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20160728 MGI PMID:23615463 62201 Rab7 RAB7, member RAS oncogene family gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20240425 MGI PMID:37878717 62201 Rab7 RAB7, member RAS oncogene family gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20160728 MGI PMID:23615463 62201 Rab7 RAB7, member RAS oncogene family gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20160728 MGI PMID:23615463 62201 Rab7 RAB7, member RAS oncogene family gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20160728 MGI PMID:23615463 62201 Rab7 RAB7, member RAS oncogene family gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20160728 MGI PMID:23615463 62201 Rab7 RAB7, member RAS oncogene family gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20160714 MGI PMID:23615463 62201 Rab7 RAB7, member RAS oncogene family gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20160728 MGI PMID:23615463 62201 Rab7 RAB7, member RAS oncogene family gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:22990867 62201 Rab7 RAB7, member RAS oncogene family gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20160728 MGI PMID:23615463 62201 Rab7 RAB7, member RAS oncogene family gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:22990867 62201 Rab7 RAB7, member RAS oncogene family gene MP:0014345 abnormal neuron mitochondrial morphology IAGP N RGD:5509061 20240425 MGI PMID:37878717 62201 Rab7 RAB7, member RAS oncogene family gene MP:0020954 decreased mechanical nociceptive threshold IAGP N RGD:5509061 20240425 MGI PMID:37878717 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11238557 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9630215 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:11238557 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:11238557 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:9630215 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17166844 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:17166844 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17166844 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17166844 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:17341595 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20190207 MGI PMID:27335465 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20190207 MGI PMID:27335465 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:19325005 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20190207 MGI PMID:27335465 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17341595 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20190207 MGI PMID:27335465 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:19325005 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20190207 MGI PMID:27335465 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16614371 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22484817 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002139 abnormal hepatobiliary system physiology IAGP N RGD:5509061 20141003 MGI PMID:16614371 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11238557 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17341595 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12524534 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:12193651 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19717840 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:9630215 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22484817 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:19325005 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20141003 MGI PMID:17341595 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:17341595 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17341595 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17341595 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20141003 MGI PMID:17166844 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:11238557 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:9630215 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22484817 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:9630215 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:19325005 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:9630215 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20141003 MGI PMID:11238557 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:17341595 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:17563384 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20141003 MGI PMID:19325005 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17166844 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17166844 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20190207 MGI PMID:27335465 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0004832 enlarged ovary IAGP N RGD:5509061 20141003 MGI PMID:19325005 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19325005 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17341595 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9630215 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22484817 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:19325005 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16614371 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22484817 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:22484817 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:9630215 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9630215 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:17166844 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:17166844 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0008717 increased lung squamous cell carcinoma incidence IAGP N RGD:5509061 20190207 MGI PMID:27335465 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:19717840 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22484817 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0009229 abnormal neurohypophysis median eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12193651 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0009648 abnormal superovulation IAGP N RGD:5509061 20141003 MGI PMID:19325005 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20141003 MGI PMID:17166844 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0009688 abnormal spinal cord central canal morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12524534 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10968783 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11238557 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22484817 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9630215 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20180111 MGI PMID:27480224 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20190207 MGI PMID:27335465 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20190207 MGI PMID:27335465 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0010901 abnormal pulmonary alveolar parenchyma morphology IAGP N RGD:5509061 20190207 MGI PMID:27335465 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0013218 abnormal substantia nigra pars reticulata morphology IAGP N RGD:5509061 20141003 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0013598 Leydig cell hypertrophy IAGP N RGD:5509061 20150319 MGI PMID:17341595 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0013908 small lateral ventricles IAGP N RGD:5509061 20161103 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0013909 small third ventricle IAGP N RGD:5509061 20161103 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0013910 small fourth ventricle IAGP N RGD:5509061 20161103 MGI PMID:12368482 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:17341595 62202 Nr1h3 nuclear receptor subfamily 1, group H, member 3 gene MP:0031063 increased erythrocyte sedimentation rate IAGP N RGD:5509061 20200618 MGI PMID:19325005 62204 Gabarap gamma-aminobutyric acid receptor associated protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16307606 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18407290 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18407290 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18407290 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:18407290 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20231207 MGI 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11772953 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:11772953 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:18407290 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:18407290 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:18407290 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:18407290 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20201022 MGI 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18407290 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:18407290 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18407290 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210826 MGI 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20210128 MGI 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:11772953 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:18407290 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:18407290 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210826 MGI 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20180215 MGI 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:18407290 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20200514 MGI 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210520 MGI 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0030636 decreased taurine level IAGP N RGD:5509061 20180913 MGI PMID:11772953 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0030639 decreased circulating taurine level IAGP N RGD:5509061 20180913 MGI PMID:11772953 62205 Slc6a6 solute carrier family 6 (neurotransmitter transporter, taurine), member 6 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:11772953 62206 Gas6 growth arrest specific 6 gene MP:0000199 abnormal circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:12122116 62206 Gas6 growth arrest specific 6 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 62206 Gas6 growth arrest specific 6 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 62206 Gas6 growth arrest specific 6 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:12122116 62206 Gas6 growth arrest specific 6 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 62206 Gas6 growth arrest specific 6 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:19729839 62206 Gas6 growth arrest specific 6 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12122116 62206 Gas6 growth arrest specific 6 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12122116 62206 Gas6 growth arrest specific 6 gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20141003 MGI PMID:11175853 62206 Gas6 growth arrest specific 6 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:11175853 62206 Gas6 growth arrest specific 6 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12122116 62206 Gas6 growth arrest specific 6 gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12122116 62206 Gas6 growth arrest specific 6 gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:12122116 62206 Gas6 growth arrest specific 6 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201001 MGI PMID:11175853 62207 Tfpi tissue factor pathway inhibitor gene MP:0000084 abnormal fontanelle morphology IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0000440 domed cranium IEA N RGD:5509061 20200604 MGI 62207 Tfpi tissue factor pathway inhibitor gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10021455 62207 Tfpi tissue factor pathway inhibitor gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0001891 hydrocephaly IEA N RGD:5509061 20200604 MGI 62207 Tfpi tissue factor pathway inhibitor gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0002083 premature death IEA N RGD:5509061 20200604 MGI 62207 Tfpi tissue factor pathway inhibitor gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:10021455 62207 Tfpi tissue factor pathway inhibitor gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:20516367 62207 Tfpi tissue factor pathway inhibitor gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0010211 abnormal acute phase protein level IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0010769 abnormal survival IAGP N RGD:5509061 20180322 MGI PMID:28827327 62207 Tfpi tissue factor pathway inhibitor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10021455 62207 Tfpi tissue factor pathway inhibitor gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20516367 62207 Tfpi tissue factor pathway inhibitor gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20180322 MGI PMID:28827327 62207 Tfpi tissue factor pathway inhibitor gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9819035 62207 Tfpi tissue factor pathway inhibitor gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180322 MGI PMID:28827327 62207 Tfpi tissue factor pathway inhibitor gene MP:0011380 enlarged brain ventricles IEA N RGD:5509061 20200604 MGI 62207 Tfpi tissue factor pathway inhibitor gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:20516367 62208 Stx6 syntaxin 6 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210826 MGI 62208 Stx6 syntaxin 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 62208 Stx6 syntaxin 6 gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 62208 Stx6 syntaxin 6 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20200514 MGI 62208 Stx6 syntaxin 6 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200514 MGI 62208 Stx6 syntaxin 6 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210826 MGI 62208 Stx6 syntaxin 6 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230601 MGI 62208 Stx6 syntaxin 6 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 62209 Fzd1 frizzled class receptor 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:20940229 62209 Fzd1 frizzled class receptor 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:20940229 62209 Fzd1 frizzled class receptor 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 62209 Fzd1 frizzled class receptor 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 62209 Fzd1 frizzled class receptor 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20940229 62209 Fzd1 frizzled class receptor 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:20940229 62209 Fzd1 frizzled class receptor 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:20940229 62209 Fzd1 frizzled class receptor 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:23095888 62209 Fzd1 frizzled class receptor 1 gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20141003 MGI PMID:20940229 62209 Fzd1 frizzled class receptor 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:20940229 62209 Fzd1 frizzled class receptor 1 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:22954793 62209 Fzd1 frizzled class receptor 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:22954793 62209 Fzd1 frizzled class receptor 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:22954793 62209 Fzd1 frizzled class receptor 1 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:22954793 62209 Fzd1 frizzled class receptor 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 62209 Fzd1 frizzled class receptor 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210826 MGI 62209 Fzd1 frizzled class receptor 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20200514 MGI 62209 Fzd1 frizzled class receptor 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:20940229 62209 Fzd1 frizzled class receptor 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:22954793 62209 Fzd1 frizzled class receptor 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:22954793 62209 Fzd1 frizzled class receptor 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:22954793 62209 Fzd1 frizzled class receptor 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 62209 Fzd1 frizzled class receptor 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 62209 Fzd1 frizzled class receptor 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20940229 62209 Fzd1 frizzled class receptor 1 gene MP:0004406 abnormal cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:20940229 62209 Fzd1 frizzled class receptor 1 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:20940229 62209 Fzd1 frizzled class receptor 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20220811 MGI 62209 Fzd1 frizzled class receptor 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 62209 Fzd1 frizzled class receptor 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 62209 Fzd1 frizzled class receptor 1 gene MP:0009094 abnormal endometrial gland morphology IAGP N RGD:5509061 20141003 MGI PMID:22954793 62209 Fzd1 frizzled class receptor 1 gene MP:0009096 decreased endometrial gland number IAGP N RGD:5509061 20141003 MGI PMID:22954793 62209 Fzd1 frizzled class receptor 1 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20141003 MGI PMID:20940229 62209 Fzd1 frizzled class receptor 1 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:20940229 62209 Fzd1 frizzled class receptor 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:20940229 62209 Fzd1 frizzled class receptor 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20940229 62209 Fzd1 frizzled class receptor 1 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20201022 MGI 62209 Fzd1 frizzled class receptor 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 62209 Fzd1 frizzled class receptor 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220811 MGI 62210 Stx8 syntaxin 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160915 MGI PMID:24652767 62210 Stx8 syntaxin 8 gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20160804 MGI 62210 Stx8 syntaxin 8 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20160225 MGI PMID:25404741 62210 Stx8 syntaxin 8 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20160225 MGI PMID:25404741 62210 Stx8 syntaxin 8 gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20160225 MGI PMID:25404741 62210 Stx8 syntaxin 8 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20160225 MGI PMID:25404741 62210 Stx8 syntaxin 8 gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20160804 MGI 62211 Slc30a1 solute carrier family 30 (zinc transporter), member 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15452870 62211 Slc30a1 solute carrier family 30 (zinc transporter), member 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15452870 62211 Slc30a1 solute carrier family 30 (zinc transporter), member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15452870 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:14578452 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14578452 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14578452 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14578452 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:14578452 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:14578452 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0002853 hyposulfatemia IAGP N RGD:5509061 20141003 MGI PMID:14578452 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:14578452 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:14578452 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:14578452 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:14578452 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:14578452 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:14578452 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0009472 increased urine sulfate level IAGP N RGD:5509061 20141003 MGI PMID:14578452 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:14578452 62212 Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1 gene MP:0031434 increased miscarriage rate IAGP N RGD:5509061 20220915 MGI PMID:14578452 62213 Slc13a2 solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 2 gene MP:0002893 ketoaciduria IAGP N RGD:5509061 20141003 MGI PMID:17410095 62213 Slc13a2 solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 2 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17410095 62214 Gpr88 G-protein coupled receptor 88 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0001394 circling IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20181025 MGI PMID:23064379 62214 Gpr88 G-protein coupled receptor 88 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20181025 MGI PMID:23064379 62214 Gpr88 G-protein coupled receptor 88 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20181025 MGI PMID:23064379 62214 Gpr88 G-protein coupled receptor 88 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20181025 MGI PMID:23064379 62214 Gpr88 G-protein coupled receptor 88 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20181025 MGI PMID:23064379 62214 Gpr88 G-protein coupled receptor 88 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20181025 MGI PMID:23064379 62214 Gpr88 G-protein coupled receptor 88 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20181025 MGI PMID:23064379 62214 Gpr88 G-protein coupled receptor 88 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20181025 MGI PMID:23064379 62214 Gpr88 G-protein coupled receptor 88 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20181025 MGI PMID:23064379 62214 Gpr88 G-protein coupled receptor 88 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20181025 MGI PMID:23064379 62214 Gpr88 G-protein coupled receptor 88 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20181025 MGI PMID:23064379 62214 Gpr88 G-protein coupled receptor 88 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20181025 MGI PMID:23064379 62214 Gpr88 G-protein coupled receptor 88 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20181025 MGI PMID:23064379 62214 Gpr88 G-protein coupled receptor 88 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20181025 MGI PMID:23064379 62214 Gpr88 G-protein coupled receptor 88 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0012293 impaired active avoidance behavior IAGP N RGD:5509061 20181025 MGI PMID:23064379 62214 Gpr88 G-protein coupled receptor 88 gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0020875 decreased nervous system dopamine level IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0020876 increased nervous system dopamine level IAGP N RGD:5509061 20201015 MGI PMID:26188600 62214 Gpr88 G-protein coupled receptor 88 gene MP:0030585 enhanced behavioral response to amphetamine IAGP N RGD:5509061 20181025 MGI PMID:23064379 62216 Ddt D-dopachrome tautomerase gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20210527 MGI PMID:24983315 62216 Ddt D-dopachrome tautomerase gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20210527 MGI PMID:24983315 62216 Ddt D-dopachrome tautomerase gene MP:0031217 increased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20210527 MGI PMID:24983315 62216 Ddt D-dopachrome tautomerase gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:24983315 62217 Aif1 allograft inflammatory factor 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20170105 MGI 62217 Aif1 allograft inflammatory factor 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 62217 Aif1 allograft inflammatory factor 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 62217 Aif1 allograft inflammatory factor 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23929822 62217 Aif1 allograft inflammatory factor 1 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:23929822 62217 Aif1 allograft inflammatory factor 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 62217 Aif1 allograft inflammatory factor 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23929822 62217 Aif1 allograft inflammatory factor 1 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 62217 Aif1 allograft inflammatory factor 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20170105 MGI 62217 Aif1 allograft inflammatory factor 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 62218 Prkce protein kinase C, epsilon gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:11696589 62218 Prkce protein kinase C, epsilon gene MP:0001123 dilated uterus IAGP N RGD:5509061 20141003 MGI PMID:11696589 62218 Prkce protein kinase C, epsilon gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11696589 62218 Prkce protein kinase C, epsilon gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:12427847 62218 Prkce protein kinase C, epsilon gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11696589 62218 Prkce protein kinase C, epsilon gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11696589 62218 Prkce protein kinase C, epsilon gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:12160964 62218 Prkce protein kinase C, epsilon gene MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:12427847 62218 Prkce protein kinase C, epsilon gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11696589 62218 Prkce protein kinase C, epsilon gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20190110 MGI 62218 Prkce protein kinase C, epsilon gene MP:0008127 decreased dendritic cell number IEA N RGD:5509061 20190110 MGI 62218 Prkce protein kinase C, epsilon gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:11696589 62218 Prkce protein kinase C, epsilon gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:14559850 62218 Prkce protein kinase C, epsilon gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:11696589 62218 Prkce protein kinase C, epsilon gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11696589 62218 Prkce protein kinase C, epsilon gene MP:0011077 decreased macrophage nitric oxide production IAGP N RGD:5509061 20141003 MGI PMID:11696589 62218 Prkce protein kinase C, epsilon gene MP:0011081 decreased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11696589 62219 Gjb1 gap junction protein, beta 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:8790370 62219 Gjb1 gap junction protein, beta 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:8790370 62219 Gjb1 gap junction protein, beta 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12805295 62219 Gjb1 gap junction protein, beta 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12843301 62219 Gjb1 gap junction protein, beta 1 gene MP:0000745 tremors IAGP N RGD:5509061 20151015 MGI PMID:25524707 62219 Gjb1 gap junction protein, beta 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:12805295 62219 Gjb1 gap junction protein, beta 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:12843301 62219 Gjb1 gap junction protein, beta 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:21750683 62219 Gjb1 gap junction protein, beta 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:9169515 62219 Gjb1 gap junction protein, beta 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:12843301 62219 Gjb1 gap junction protein, beta 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:9169515 62219 Gjb1 gap junction protein, beta 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:9700485 62219 Gjb1 gap junction protein, beta 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20151015 MGI PMID:25524707 62219 Gjb1 gap junction protein, beta 1 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:12805295 62219 Gjb1 gap junction protein, beta 1 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20151015 MGI PMID:25524707 62219 Gjb1 gap junction protein, beta 1 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9169515 62219 Gjb1 gap junction protein, beta 1 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9700485 62219 Gjb1 gap junction protein, beta 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8790370 62219 Gjb1 gap junction protein, beta 1 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:12843301 62219 Gjb1 gap junction protein, beta 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21750683 62219 Gjb1 gap junction protein, beta 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20151015 MGI PMID:25524707 62219 Gjb1 gap junction protein, beta 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20151015 MGI PMID:25524707 62219 Gjb1 gap junction protein, beta 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:12805295 62219 Gjb1 gap junction protein, beta 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:21750683 62219 Gjb1 gap junction protein, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12805295 62219 Gjb1 gap junction protein, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12843301 62219 Gjb1 gap junction protein, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21750683 62219 Gjb1 gap junction protein, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20151015 MGI PMID:25524707 62219 Gjb1 gap junction protein, beta 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:12805295 62219 Gjb1 gap junction protein, beta 1 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:12805295 62219 Gjb1 gap junction protein, beta 1 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:12843301 62219 Gjb1 gap junction protein, beta 1 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20151015 MGI PMID:25524707 62219 Gjb1 gap junction protein, beta 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21750683 62219 Gjb1 gap junction protein, beta 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20151015 MGI PMID:25524707 62219 Gjb1 gap junction protein, beta 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:9169515 62219 Gjb1 gap junction protein, beta 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:9700485 62219 Gjb1 gap junction protein, beta 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:9700485 62219 Gjb1 gap junction protein, beta 1 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:9169515 62219 Gjb1 gap junction protein, beta 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:9169515 62219 Gjb1 gap junction protein, beta 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:9700485 62219 Gjb1 gap junction protein, beta 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20151015 MGI PMID:25524707 62219 Gjb1 gap junction protein, beta 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20151015 MGI PMID:25524707 62219 Gjb1 gap junction protein, beta 1 gene MP:0010205 abnormal oligodendrocyte apoptosis IAGP N RGD:5509061 20151015 MGI PMID:25524707 62219 Gjb1 gap junction protein, beta 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:8790370 62219 Gjb1 gap junction protein, beta 1 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20151015 MGI PMID:25524707 62219 Gjb1 gap junction protein, beta 1 gene MP:0030987 spinal cord inflammation IAGP N RGD:5509061 20191128 MGI PMID:25524707 62219 Gjb1 gap junction protein, beta 1 gene MP:0030991 optic nerve inflammation IAGP N RGD:5509061 20191128 MGI PMID:25524707 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0000532 kidney vascular congestion IAGP N RGD:5509061 20200310 MGI PMID:15632011 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20200310 MGI PMID:16377626 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20200310 MGI PMID:15890968 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200310 MGI PMID:15632011 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20200310 MGI PMID:14613294 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20200310 MGI PMID:14613294 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200310 MGI PMID:15632011 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20200310 MGI PMID:15632011 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20200310 MGI PMID:19180231 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20200310 MGI PMID:14613294 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20200310 MGI PMID:15632011 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20200310 MGI PMID:16166207 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20200310 MGI PMID:19048083 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20200310 MGI PMID:15890968 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20200310 MGI PMID:16166207 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20200310 MGI PMID:16377626 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20200310 MGI PMID:14613294 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0009864 abnormal aorta endothelium morphology IAGP N RGD:5509061 20200310 MGI PMID:19048083 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20200310 MGI PMID:15632011 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20200310 MGI PMID:15632011 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0010020 spleen vascular congestion IAGP N RGD:5509061 20200310 MGI PMID:15632011 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20200310 MGI PMID:16377626 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0011134 decreased lung endothelial cell migration IAGP N RGD:5509061 20200310 MGI PMID:16377626 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0011433 glomerular capillary congestion IAGP N RGD:5509061 20200310 MGI PMID:15632011 62220 Pecam1 platelet/endothelial cell adhesion molecule 1 gene MP:0014473 increased pulmonary alveolus wall thickness IAGP N RGD:5509061 20240704 MGI PMID:16377626 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17548584 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:24121508 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000288 abnormal pericardium morphology IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17142669 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20399150 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:23264599 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16510575 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12620994 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12972594 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000801 abnormal temporal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:12972594 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000804 abnormal occipital lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:12972594 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18332118 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:15328538 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:18801745 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:18801745 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:18586877 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:18586877 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12972594 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17334357 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:18801745 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:15798202 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15132980 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:15489957 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:16510872 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:9606183 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9606183 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:9606183 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16510872 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:16510575 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:18037992 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12628185 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:12620994 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:12972594 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:17554006 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23264599 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16510872 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:18801745 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:17142669 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002047 increased hepatic hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:15798202 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15328538 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23264599 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24121508 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:16510872 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:15328538 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16510575 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22995899 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22995899 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15781641 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16510872 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:18801745 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18801745 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18801745 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002332 abnormal exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:15328538 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17111048 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12628185 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22464323 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:23264599 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:24121508 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15798202 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20220721 MGI PMID:34329568 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18586877 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:15798202 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20220721 MGI PMID:34329568 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:15542432 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:17554006 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:18037992 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:22539295 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15843612 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:12972594 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:12972594 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:19643083 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:12628185 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:15542432 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:15542432 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:16510575 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12628185 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:16510872 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:15132980 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15132980 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18037992 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19643083 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:12620994 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:15132980 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:15132980 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:18801745 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:9606183 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20220721 MGI PMID:34329568 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22995899 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18332118 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:9606183 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20220721 MGI PMID:34329568 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17554006 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17554006 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:24121508 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:9606183 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18037992 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15132980 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:17111048 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:18037992 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20220721 MGI PMID:34329568 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20220721 MGI PMID:34329568 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16510872 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20141003 MGI PMID:17334357 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005535 abnormal body temperature IAGP N RGD:5509061 20141003 MGI PMID:17548584 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19643083 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:15798202 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15542432 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17334357 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:9606183 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22539295 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:18801745 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20220721 MGI PMID:34329568 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:15798202 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:15843612 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:17554006 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:17554006 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:17142669 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008125 abnormal dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22539295 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12972594 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:12972594 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:15489957 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:12972594 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008556 abnormal tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22539295 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17015677 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:12628185 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17548584 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17015677 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:17015677 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:17548584 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008656 abnormal interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22539295 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:17548584 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:17548584 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17548584 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:17015677 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17548584 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008796 increased lens fiber apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18586877 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22995899 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15132980 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17554006 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20190207 MGI PMID:24731446 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22464323 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12620994 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12620994 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17554006 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17548584 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:15328538 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20220721 MGI PMID:34329568 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20220721 MGI PMID:34329568 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:19643083 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15132980 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0010642 absent third pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:15132980 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:15132980 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22995899 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:22464323 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:22464323 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11691837 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18801745 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12972594 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16510872 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16510872 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14659802 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:22464323 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0011286 decreased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:22464323 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0011287 increased erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:24121508 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0012265 increased hindbrain size IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0012492 pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0012493 absent pharyngeal arch arteries IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:9436976 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:9606183 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20220721 MGI PMID:34329568 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0020316 decreased vascular endothelial cell proliferation IAGP N RGD:5509061 20160616 MGI PMID:15542432 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20220721 MGI PMID:34329568 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0020890 abnormal milk sodium level IAGP N RGD:5509061 20191226 MGI PMID:12620994 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:15132980 62221 Hif1a hypoxia inducible factor 1, alpha subunit gene MP:0031324 delayed liver regeneration IAGP N RGD:5509061 20220106 MGI PMID:19643083 62222 Preb prolactin regulatory element binding gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220811 MGI 62222 Preb prolactin regulatory element binding gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 62222 Preb prolactin regulatory element binding gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 62222 Preb prolactin regulatory element binding gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 62223 Sart1 squamous cell carcinoma antigen recognized by T cells 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210826 MGI 62223 Sart1 squamous cell carcinoma antigen recognized by T cells 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62223 Sart1 squamous cell carcinoma antigen recognized by T cells 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 62223 Sart1 squamous cell carcinoma antigen recognized by T cells 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210826 MGI 62224 Zfp292 zinc finger protein 292 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20220721 MGI PMID:28319097 62224 Zfp292 zinc finger protein 292 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20220721 MGI PMID:28319097 62224 Zfp292 zinc finger protein 292 gene MP:0013893 decreased common lymphocyte progenitor cell number IAGP N RGD:5509061 20220721 MGI PMID:28319097 62225 Fah fumarylacetoacetate hydrolase gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:8253378 62225 Fah fumarylacetoacetate hydrolase gene MP:0000203 abnormal circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:8253378 62225 Fah fumarylacetoacetate hydrolase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220519 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0000274 enlarged heart IEA N RGD:5509061 20220519 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:10518553 62225 Fah fumarylacetoacetate hydrolase gene MP:0000601 small liver IEA N RGD:5509061 20220519 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:10518553 62225 Fah fumarylacetoacetate hydrolase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10518553 62225 Fah fumarylacetoacetate hydrolase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:10518553 62225 Fah fumarylacetoacetate hydrolase gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:10518553 62225 Fah fumarylacetoacetate hydrolase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220811 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220811 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220519 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0001148 enlarged testis IEA N RGD:5509061 20220519 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10518553 62225 Fah fumarylacetoacetate hydrolase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0001501 abnormal sleep pattern IEA N RGD:5509061 20170824 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20230601 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210826 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0001785 edema IEA N RGD:5509061 20230601 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:10518553 62225 Fah fumarylacetoacetate hydrolase gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0002658 abnormal liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:10518553 62225 Fah fumarylacetoacetate hydrolase gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0002989 small kidney IEA N RGD:5509061 20220811 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210826 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0003326 liver failure IAGP N RGD:5509061 20141003 MGI PMID:14767996 62225 Fah fumarylacetoacetate hydrolase gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210826 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:8253378 62225 Fah fumarylacetoacetate hydrolase gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0008891 decreased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14767996 62225 Fah fumarylacetoacetate hydrolase gene MP:0008987 abnormal liver lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0009110 pancreas hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10224267 62225 Fah fumarylacetoacetate hydrolase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:14767996 62225 Fah fumarylacetoacetate hydrolase gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0010384 increased renal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18598944 62225 Fah fumarylacetoacetate hydrolase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10224267 62225 Fah fumarylacetoacetate hydrolase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10224267 62225 Fah fumarylacetoacetate hydrolase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8253378 62225 Fah fumarylacetoacetate hydrolase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 62225 Fah fumarylacetoacetate hydrolase gene MP:0012602 increased alpha-fetoprotein level IAGP N RGD:5509061 20141003 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0013723 increased circulating tyrosine level IAGP N RGD:5509061 20150409 MGI PMID:10518553 62225 Fah fumarylacetoacetate hydrolase gene MP:0013723 increased circulating tyrosine level IAGP N RGD:5509061 20150409 MGI PMID:7545495 62225 Fah fumarylacetoacetate hydrolase gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:7545495 62228 Pla2g10 phospholipase A2, group X gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18506007 62228 Pla2g10 phospholipase A2, group X gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 62228 Pla2g10 phospholipase A2, group X gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20170105 MGI 62228 Pla2g10 phospholipase A2, group X gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 62228 Pla2g10 phospholipase A2, group X gene MP:0001744 hypersecretion of corticosterone IAGP N RGD:5509061 20141003 MGI PMID:20421306 62228 Pla2g10 phospholipase A2, group X gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:20421306 62228 Pla2g10 phospholipase A2, group X gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17403936 62228 Pla2g10 phospholipase A2, group X gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:18506007 62228 Pla2g10 phospholipase A2, group X gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:17403936 62228 Pla2g10 phospholipase A2, group X gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18506007 62228 Pla2g10 phospholipase A2, group X gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:18506007 62228 Pla2g10 phospholipase A2, group X gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20220811 MGI 62228 Pla2g10 phospholipase A2, group X gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:20424323 62228 Pla2g10 phospholipase A2, group X gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20220811 MGI 62228 Pla2g10 phospholipase A2, group X gene MP:0004156 abnormal QT variability IEA N RGD:5509061 20220811 MGI 62228 Pla2g10 phospholipase A2, group X gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:18506007 62228 Pla2g10 phospholipase A2, group X gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17403936 62228 Pla2g10 phospholipase A2, group X gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17403936 62228 Pla2g10 phospholipase A2, group X gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220811 MGI 62228 Pla2g10 phospholipase A2, group X gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20220811 MGI 62228 Pla2g10 phospholipase A2, group X gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17403936 62228 Pla2g10 phospholipase A2, group X gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17403936 62228 Pla2g10 phospholipase A2, group X gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:18506007 62228 Pla2g10 phospholipase A2, group X gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:17403936 62228 Pla2g10 phospholipase A2, group X gene MP:0009811 abnormal prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:17403936 62228 Pla2g10 phospholipase A2, group X gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 62228 Pla2g10 phospholipase A2, group X gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220811 MGI 62229 Slc22a2 solute carrier family 22 (organic cation transporter), member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14560032 62229 Slc22a2 solute carrier family 22 (organic cation transporter), member 2 gene MP:0006273 abnormal urine organic cation level IAGP N RGD:5509061 20141003 MGI PMID:14560032 62230 Nrbf2 nuclear receptor binding factor 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20191226 MGI PMID:24849286 62230 Nrbf2 nuclear receptor binding factor 2 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20191226 MGI PMID:24849286 62230 Nrbf2 nuclear receptor binding factor 2 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20191226 MGI PMID:24849286 62230 Nrbf2 nuclear receptor binding factor 2 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20191226 MGI PMID:24849286 62230 Nrbf2 nuclear receptor binding factor 2 gene MP:0030939 abnormal autophagosome formation IAGP N RGD:5509061 20191226 MGI PMID:24849286 62230 Nrbf2 nuclear receptor binding factor 2 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20191226 MGI PMID:24849286 62231 Fau FAU ubiquitin like and ribosomal protein S30 fusion gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200917 MGI PMID:26031240 62231 Fau FAU ubiquitin like and ribosomal protein S30 fusion gene MP:0003718 maternal effect IAGP N RGD:5509061 20200917 MGI PMID:26031240 62231 Fau FAU ubiquitin like and ribosomal protein S30 fusion gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20200917 MGI PMID:26031240 62231 Fau FAU ubiquitin like and ribosomal protein S30 fusion gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200917 MGI PMID:26031240 62232 Nckap1 NCK-associated protein 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15755804 62232 Nckap1 NCK-associated protein 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15755804 62232 Nckap1 NCK-associated protein 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:21693517 62232 Nckap1 NCK-associated protein 1 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21693517 62232 Nckap1 NCK-associated protein 1 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 62232 Nckap1 NCK-associated protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20141003 MGI PMID:20689803 62232 Nckap1 NCK-associated protein 1 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:15755804 62232 Nckap1 NCK-associated protein 1 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:16831833 62232 Nckap1 NCK-associated protein 1 gene MP:0012156 rostral-caudal axis duplication IAGP N RGD:5509061 20141003 MGI PMID:16831833 62234 Robo1 roundabout guidance receptor 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20231123 MGI PMID:28592524 62234 Robo1 roundabout guidance receptor 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231123 MGI PMID:28592524 62234 Robo1 roundabout guidance receptor 1 gene MP:0000276 heart right ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 62234 Robo1 roundabout guidance receptor 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231123 MGI PMID:28592524 62234 Robo1 roundabout guidance receptor 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20231123 MGI PMID:28592524 62234 Robo1 roundabout guidance receptor 1 gene MP:0000445 short snout IAGP N RGD:5509061 20231123 MGI PMID:28592524 62234 Robo1 roundabout guidance receptor 1 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:23328398 62234 Robo1 roundabout guidance receptor 1 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20141003 MGI 62234 Robo1 roundabout guidance receptor 1 gene MP:0000536 hydroureter IEA N RGD:5509061 20141003 MGI 62234 Robo1 roundabout guidance receptor 1 gene MP:0000653 abnormal sex gland morphology IEA N RGD:5509061 20141003 MGI 62234 Robo1 roundabout guidance receptor 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:16690755 62234 Robo1 roundabout guidance receptor 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:16690755 62234 Robo1 roundabout guidance receptor 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:17392456 62234 Robo1 roundabout guidance receptor 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11734623 62234 Robo1 roundabout guidance receptor 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:11734623 62234 Robo1 roundabout guidance receptor 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:11734623 62234 Robo1 roundabout guidance receptor 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 62234 Robo1 roundabout guidance receptor 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 62234 Robo1 roundabout guidance receptor 1 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 62234 Robo1 roundabout guidance receptor 1 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:11734623 62234 Robo1 roundabout guidance receptor 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:23328398 62234 Robo1 roundabout guidance receptor 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11734623 62234 Robo1 roundabout guidance receptor 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:23328398 62234 Robo1 roundabout guidance receptor 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15374951 62234 Robo1 roundabout guidance receptor 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15374951 62234 Robo1 roundabout guidance receptor 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23328398 62234 Robo1 roundabout guidance receptor 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20141003 MGI 62234 Robo1 roundabout guidance receptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23328398 62234 Robo1 roundabout guidance receptor 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:17392456 62234 Robo1 roundabout guidance receptor 1 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16690755 62234 Robo1 roundabout guidance receptor 1 gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:11734623 62234 Robo1 roundabout guidance receptor 1 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:11734623 62234 Robo1 roundabout guidance receptor 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:11734623 62234 Robo1 roundabout guidance receptor 1 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:23328398 62234 Robo1 roundabout guidance receptor 1 gene MP:0002625 heart left ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 62234 Robo1 roundabout guidance receptor 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20231123 MGI PMID:28592524 62234 Robo1 roundabout guidance receptor 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15084255 62234 Robo1 roundabout guidance receptor 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15091338 62234 Robo1 roundabout guidance receptor 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:16690755 62234 Robo1 roundabout guidance receptor 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:17360927 62234 Robo1 roundabout guidance receptor 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:17392456 62234 Robo1 roundabout guidance receptor 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:16690755 62234 Robo1 roundabout guidance receptor 1 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:23328398 62234 Robo1 roundabout guidance receptor 1 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:18054781 62234 Robo1 roundabout guidance receptor 1 gene MP:0004550 short trachea IAGP N RGD:5509061 20141003 MGI PMID:23328398 62234 Robo1 roundabout guidance receptor 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:23328398 62234 Robo1 roundabout guidance receptor 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 62234 Robo1 roundabout guidance receptor 1 gene MP:0005237 abnormal olfactory tract morphology IAGP N RGD:5509061 20141003 MGI PMID:17360927 62234 Robo1 roundabout guidance receptor 1 gene MP:0005488 bronchial epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11734623 62234 Robo1 roundabout guidance receptor 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:16690755 62234 Robo1 roundabout guidance receptor 1 gene MP:0008219 abnormal dorsal telencephalic commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:17392456 62234 Robo1 roundabout guidance receptor 1 gene MP:0008221 abnormal hippocampal commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16690755 62234 Robo1 roundabout guidance receptor 1 gene MP:0008222 decreased hippocampal commissure size IAGP N RGD:5509061 20141003 MGI PMID:16690755 62234 Robo1 roundabout guidance receptor 1 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:17392456 62234 Robo1 roundabout guidance receptor 1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:18054781 62234 Robo1 roundabout guidance receptor 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20141003 MGI 62234 Robo1 roundabout guidance receptor 1 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16439476 62234 Robo1 roundabout guidance receptor 1 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18829537 62234 Robo1 roundabout guidance receptor 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:23328398 62234 Robo1 roundabout guidance receptor 1 gene MP:0009678 abnormal spinal cord lateral column morphology IAGP N RGD:5509061 20141003 MGI PMID:15091338 62234 Robo1 roundabout guidance receptor 1 gene MP:0009695 abnormal spinal cord ventral commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:23217742 62234 Robo1 roundabout guidance receptor 1 gene MP:0010173 increased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18829537 62234 Robo1 roundabout guidance receptor 1 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141003 MGI 62234 Robo1 roundabout guidance receptor 1 gene MP:0010405 ostium secundum atrial septal defect IAGP N RGD:5509061 20231123 MGI PMID:28592524 62234 Robo1 roundabout guidance receptor 1 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20231123 MGI PMID:28592524 62234 Robo1 roundabout guidance receptor 1 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20231123 MGI PMID:28592524 62234 Robo1 roundabout guidance receptor 1 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20231123 MGI PMID:28592524 62234 Robo1 roundabout guidance receptor 1 gene MP:0010807 abnormal stomach position or orientation IAGP N RGD:5509061 20141003 MGI PMID:23328398 62234 Robo1 roundabout guidance receptor 1 gene MP:0010880 small esophagus IAGP N RGD:5509061 20141003 MGI PMID:23328398 62234 Robo1 roundabout guidance receptor 1 gene MP:0010881 esophagus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23328398 62234 Robo1 roundabout guidance receptor 1 gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20141003 MGI PMID:11734623 62234 Robo1 roundabout guidance receptor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23328398 62234 Robo1 roundabout guidance receptor 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11734623 62234 Robo1 roundabout guidance receptor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16690755 62234 Robo1 roundabout guidance receptor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 62234 Robo1 roundabout guidance receptor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 62234 Robo1 roundabout guidance receptor 1 gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20141003 MGI PMID:23328398 62234 Robo1 roundabout guidance receptor 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15374951 62234 Robo1 roundabout guidance receptor 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 62235 Pde3a phosphodiesterase 3A, cGMP inhibited gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15254586 62235 Pde3a phosphodiesterase 3A, cGMP inhibited gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 62235 Pde3a phosphodiesterase 3A, cGMP inhibited gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:15254586 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0003441 increased glycerol level IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0004357 long tibia IEA N RGD:5509061 20190502 MGI 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17143332 62236 Pde3b phosphodiesterase 3B, cGMP-inhibited gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:17143332 62237 Chka choline kinase alpha gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18029352 62237 Chka choline kinase alpha gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18029352 62237 Chka choline kinase alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62238 Per2 period circadian clock 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20171012 MGI PMID:25288642 62238 Per2 period circadian clock 2 gene MP:0000619 salivary gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12372299 62238 Per2 period circadian clock 2 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:18367514 62238 Per2 period circadian clock 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18367514 62238 Per2 period circadian clock 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23193187 62238 Per2 period circadian clock 2 gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:18367514 62238 Per2 period circadian clock 2 gene MP:0001432 abnormal food preference IAGP N RGD:5509061 20141003 MGI PMID:18367514 62238 Per2 period circadian clock 2 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:15031135 62238 Per2 period circadian clock 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23193187 62238 Per2 period circadian clock 2 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:12372299 62238 Per2 period circadian clock 2 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:23267082 62238 Per2 period circadian clock 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:18367514 62238 Per2 period circadian clock 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18367514 62238 Per2 period circadian clock 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20141003 MGI 62238 Per2 period circadian clock 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12372299 62238 Per2 period circadian clock 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:16143109 62238 Per2 period circadian clock 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14963227 62238 Per2 period circadian clock 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16143109 62238 Per2 period circadian clock 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:23193187 62238 Per2 period circadian clock 2 gene MP:0002717 abnormal male preputial gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12372299 62238 Per2 period circadian clock 2 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23193187 62238 Per2 period circadian clock 2 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 62238 Per2 period circadian clock 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20141003 MGI 62238 Per2 period circadian clock 2 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:12372299 62238 Per2 period circadian clock 2 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:23193187 62238 Per2 period circadian clock 2 gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:12372299 62238 Per2 period circadian clock 2 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:23193187 62238 Per2 period circadian clock 2 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:16143109 62238 Per2 period circadian clock 2 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:20634945 62238 Per2 period circadian clock 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:15031135 62238 Per2 period circadian clock 2 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20171012 MGI PMID:26392540 62238 Per2 period circadian clock 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200310 MGI PMID:23193187 62238 Per2 period circadian clock 2 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:18367514 62238 Per2 period circadian clock 2 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:16143109 62238 Per2 period circadian clock 2 gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20171012 MGI PMID:26232227 62238 Per2 period circadian clock 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16143109 62238 Per2 period circadian clock 2 gene MP:0008779 abnormal maternal behavior IAGP N RGD:5509061 20141003 MGI PMID:18367514 62238 Per2 period circadian clock 2 gene MP:0008961 abnormal basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:18367514 62238 Per2 period circadian clock 2 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:18367514 62238 Per2 period circadian clock 2 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:18367514 62238 Per2 period circadian clock 2 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:18367514 62238 Per2 period circadian clock 2 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:18367514 62238 Per2 period circadian clock 2 gene MP:0009713 enhanced conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:12084940 62238 Per2 period circadian clock 2 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:12084940 62238 Per2 period circadian clock 2 gene MP:0010318 increased salivary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12372299 62238 Per2 period circadian clock 2 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23193187 62238 Per2 period circadian clock 2 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:20634945 62238 Per2 period circadian clock 2 gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15031135 62238 Per2 period circadian clock 2 gene MP:0011478 abnormal urine catecholamine level IAGP N RGD:5509061 20141003 MGI PMID:16143109 62238 Per2 period circadian clock 2 gene MP:0011903 decreased hematopoietic stem cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23193187 62238 Per2 period circadian clock 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12372299 62238 Per2 period circadian clock 2 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:20634945 62238 Per2 period circadian clock 2 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:20634945 62238 Per2 period circadian clock 2 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20171012 MGI PMID:23267082 62238 Per2 period circadian clock 2 gene MP:0020467 abnormal circadian behavior IEA N RGD:5509061 20180927 MGI 62238 Per2 period circadian clock 2 gene MP:0020468 abnormal circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:23580255 62238 Per2 period circadian clock 2 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:17218255 62238 Per2 period circadian clock 2 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20240118 MGI PMID:36638184 62238 Per2 period circadian clock 2 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:10408444 62238 Per2 period circadian clock 2 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:12372299 62238 Per2 period circadian clock 2 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:17218255 62238 Per2 period circadian clock 2 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:10408444 62238 Per2 period circadian clock 2 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:11389837 62238 Per2 period circadian clock 2 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:11395012 62238 Per2 period circadian clock 2 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:12372299 62238 Per2 period circadian clock 2 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:12381662 62238 Per2 period circadian clock 2 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:15031135 62238 Per2 period circadian clock 2 gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20240118 MGI PMID:36638184 62238 Per2 period circadian clock 2 gene MP:0020475 delayed circadian behavior phase IEA N RGD:5509061 20180927 MGI 62238 Per2 period circadian clock 2 gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20240118 MGI PMID:36638184 62238 Per2 period circadian clock 2 gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20171012 MGI PMID:10408444 62238 Per2 period circadian clock 2 gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20240118 MGI PMID:36638184 62238 Per2 period circadian clock 2 gene MP:0020478 abnormal circadian sleep/wake cycle IAGP N RGD:5509061 20171012 MGI PMID:12383239 62238 Per2 period circadian clock 2 gene MP:0030438 increased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:16143109 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8543156 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11859196 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11859196 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12130536 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:11859196 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:12130536 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:12130536 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:8543155 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:8543156 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:11859196 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:12130536 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:12130536 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:12782656 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:8543156 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:8543156 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8543156 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8543155 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:8543156 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:8543155 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:11859196 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8543155 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:12130536 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0004164 abnormal neurohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:8543155 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0004164 abnormal neurohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:8543156 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:12130536 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0004979 abnormal neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:8543155 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:12782656 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12130536 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:12130536 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:12130536 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12130536 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:8543155 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8543155 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8543156 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12130536 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11859196 62239 Pou3f2 POU domain, class 3, transcription factor 2 gene MP:0013340 abnormal pituicyte morphology IAGP N RGD:5509061 20141204 MGI PMID:8543156 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:10464101 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:12062767 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20160107 MGI PMID:23606368 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0001394 circling IAGP N RGD:5509061 20160107 MGI PMID:23606368 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:16235133 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:10587581 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20160107 MGI PMID:23606368 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:10464101 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:12062767 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0001967 deafness IAGP N RGD:5509061 20160107 MGI PMID:23606368 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0002730 head shaking IEA N RGD:5509061 20111116 MGI 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:10587581 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:15655183 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20160107 MGI PMID:23606368 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0003167 abnormal scala tympani morphology IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004286 abnormal internal auditory canal morphology IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004287 abnormal spiral limbus morphology IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004289 abnormal bony labyrinth IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004290 abnormal stapes footplate morphology IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004290 abnormal stapes footplate morphology IAGP N RGD:5509061 20141003 MGI PMID:15574296 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004292 abnormal spiral ligament fibrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004292 abnormal spiral ligament fibrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10464101 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004292 abnormal spiral ligament fibrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10587581 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004293 abnormal type I spiral ligament fibrocytes IAGP N RGD:5509061 20141003 MGI PMID:10464101 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004294 abnormal type II spiral ligament fibrocytes IAGP N RGD:5509061 20141003 MGI PMID:10464101 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004294 abnormal type II spiral ligament fibrocytes IAGP N RGD:5509061 20141003 MGI PMID:12062767 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20160107 MGI PMID:23606368 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:10464101 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:15574296 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004479 abnormal oval window morphology IAGP N RGD:5509061 20141003 MGI PMID:15574296 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20141003 MGI PMID:15574296 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:15574296 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20160107 MGI PMID:23606368 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0004862 small scala tympani IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:15574296 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0005307 head tossing IAGP N RGD:5509061 20160107 MGI PMID:23606368 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20160107 MGI PMID:23606368 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0006021 abnormal Reissner membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0006023 detached Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:12062767 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0006025 distended Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20160107 MGI PMID:23606368 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20160107 MGI PMID:23606368 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0009822 abnormal subarcuate fossa morphology IAGP N RGD:5509061 20181025 MGI PMID:10407036 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:10464101 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12062767 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15574296 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20160107 MGI PMID:23606368 62240 Pou3f4 POU domain, class 3, transcription factor 4 gene MP:0030407 abnormal stapes crus morpholgy IAGP N RGD:5509061 20171207 MGI PMID:15574296 62241 Tmod2 tropomodulin 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 62241 Tmod2 tropomodulin 2 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20201022 MGI 62241 Tmod2 tropomodulin 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220428 MGI 62241 Tmod2 tropomodulin 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12799133 62241 Tmod2 tropomodulin 2 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 62241 Tmod2 tropomodulin 2 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12799133 62241 Tmod2 tropomodulin 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12799133 62241 Tmod2 tropomodulin 2 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12799133 62241 Tmod2 tropomodulin 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:12799133 62241 Tmod2 tropomodulin 2 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12799133 62241 Tmod2 tropomodulin 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 62241 Tmod2 tropomodulin 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 62241 Tmod2 tropomodulin 2 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12799133 62241 Tmod2 tropomodulin 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 62241 Tmod2 tropomodulin 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20170105 MGI 62241 Tmod2 tropomodulin 2 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:12799133 62241 Tmod2 tropomodulin 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 62241 Tmod2 tropomodulin 2 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20201231 MGI 62241 Tmod2 tropomodulin 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 62241 Tmod2 tropomodulin 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:12799133 62242 Pla2g1b phospholipase A2, group IB, pancreas gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12376327 62242 Pla2g1b phospholipase A2, group IB, pancreas gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12376327 62242 Pla2g1b phospholipase A2, group IB, pancreas gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12376327 62242 Pla2g1b phospholipase A2, group IB, pancreas gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12376327 62242 Pla2g1b phospholipase A2, group IB, pancreas gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12376327 62242 Pla2g1b phospholipase A2, group IB, pancreas gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12376327 62242 Pla2g1b phospholipase A2, group IB, pancreas gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:12376327 62242 Pla2g1b phospholipase A2, group IB, pancreas gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12376327 62242 Pla2g1b phospholipase A2, group IB, pancreas gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:12376327 62242 Pla2g1b phospholipase A2, group IB, pancreas gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12376327 62242 Pla2g1b phospholipase A2, group IB, pancreas gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12376327 62242 Pla2g1b phospholipase A2, group IB, pancreas gene MP:0009307 decreased uterine fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12376327 62244 Lgals7 lectin, galactose binding, soluble 7 gene MP:0001203 increased sensitivity to skin irradiation IAGP N RGD:5509061 20181220 MGI PMID:18829868 62244 Lgals7 lectin, galactose binding, soluble 7 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20150430 MGI 62244 Lgals7 lectin, galactose binding, soluble 7 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20181220 MGI PMID:18829868 62244 Lgals7 lectin, galactose binding, soluble 7 gene MP:0003443 increased circulating glycerol level IEA N RGD:5509061 20150430 MGI 62244 Lgals7 lectin, galactose binding, soluble 7 gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20181220 MGI PMID:18829868 62244 Lgals7 lectin, galactose binding, soluble 7 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20181220 MGI PMID:18829868 62244 Lgals7 lectin, galactose binding, soluble 7 gene MP:0012194 decreased keratinocyte migration IAGP N RGD:5509061 20181220 MGI PMID:18829868 62245 Atp1a4 ATPase, Na+/K+ transporting, alpha 4 polypeptide gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:21187400 62245 Atp1a4 ATPase, Na+/K+ transporting, alpha 4 polypeptide gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21187400 62245 Atp1a4 ATPase, Na+/K+ transporting, alpha 4 polypeptide gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23229519 62245 Atp1a4 ATPase, Na+/K+ transporting, alpha 4 polypeptide gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21187400 62245 Atp1a4 ATPase, Na+/K+ transporting, alpha 4 polypeptide gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20141003 MGI PMID:21187400 62245 Atp1a4 ATPase, Na+/K+ transporting, alpha 4 polypeptide gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:21187400 62245 Atp1a4 ATPase, Na+/K+ transporting, alpha 4 polypeptide gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21187400 62245 Atp1a4 ATPase, Na+/K+ transporting, alpha 4 polypeptide gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:21187400 62245 Atp1a4 ATPase, Na+/K+ transporting, alpha 4 polypeptide gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:23229519 62245 Atp1a4 ATPase, Na+/K+ transporting, alpha 4 polypeptide gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20141003 MGI PMID:23229519 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:21499899 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21499899 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20190509 MGI PMID:30134165 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20190509 MGI PMID:30134165 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20190509 MGI PMID:30134165 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20190509 MGI PMID:30134165 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20190509 MGI PMID:30134165 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21499899 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20190509 MGI PMID:30134165 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21499899 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20190502 MGI 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20190509 MGI PMID:30134165 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:21499899 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23335370 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21499899 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:21499899 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20190509 MGI PMID:30134165 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20190509 MGI PMID:30134165 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20190509 MGI PMID:30134165 62246 Pak2 p21 (RAC1) activated kinase 2 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20190509 MGI PMID:30134165 62247 Gal galanin and GMAP prepropeptide gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:9770544 62247 Gal galanin and GMAP prepropeptide gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:10934278 62247 Gal galanin and GMAP prepropeptide gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:11016970 62247 Gal galanin and GMAP prepropeptide gene MP:0001021 small L4 dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:11016970 62247 Gal galanin and GMAP prepropeptide gene MP:0001024 small L5 dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:11016970 62247 Gal galanin and GMAP prepropeptide gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:12559120 62247 Gal galanin and GMAP prepropeptide gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15044363 62247 Gal galanin and GMAP prepropeptide gene MP:0001746 abnormal pituitary secretion IAGP N RGD:5509061 20141003 MGI PMID:12845222 62247 Gal galanin and GMAP prepropeptide gene MP:0001746 abnormal pituitary secretion IAGP N RGD:5509061 20141003 MGI PMID:9770544 62247 Gal galanin and GMAP prepropeptide gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:9770544 62247 Gal galanin and GMAP prepropeptide gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10934278 62247 Gal galanin and GMAP prepropeptide gene MP:0002163 abnormal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9770544 62247 Gal galanin and GMAP prepropeptide gene MP:0002164 abnormal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:9770544 62247 Gal galanin and GMAP prepropeptide gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:10934278 62247 Gal galanin and GMAP prepropeptide gene MP:0002997 enlarged seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:12845222 62247 Gal galanin and GMAP prepropeptide gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10934278 62247 Gal galanin and GMAP prepropeptide gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15044363 62247 Gal galanin and GMAP prepropeptide gene MP:0003063 increased coping response IAGP N RGD:5509061 20200402 MGI PMID:32065256 62247 Gal galanin and GMAP prepropeptide gene MP:0003368 decreased circulating glucocorticoid level IAGP N RGD:5509061 20141003 MGI PMID:12845222 62247 Gal galanin and GMAP prepropeptide gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12845222 62247 Gal galanin and GMAP prepropeptide gene MP:0004858 abnormal nervous system regeneration IAGP N RGD:5509061 20141003 MGI PMID:11016970 62247 Gal galanin and GMAP prepropeptide gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:15041741 62247 Gal galanin and GMAP prepropeptide gene MP:0008332 decreased lactotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9770544 62247 Gal galanin and GMAP prepropeptide gene MP:0010249 lactation failure IAGP N RGD:5509061 20150409 MGI PMID:9770544 62247 Gal galanin and GMAP prepropeptide gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20200402 MGI PMID:32065256 62247 Gal galanin and GMAP prepropeptide gene MP:0014269 decreased testes secretion IAGP N RGD:5509061 20230810 MGI PMID:12845222 62247 Gal galanin and GMAP prepropeptide gene MP:0014440 increased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:12845222 62248 Prps1 phosphoribosyl pyrophosphate synthetase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62249 Nt5e 5' nucleotidase, ecto gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 62249 Nt5e 5' nucleotidase, ecto gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 62249 Nt5e 5' nucleotidase, ecto gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:17353435 62249 Nt5e 5' nucleotidase, ecto gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 62249 Nt5e 5' nucleotidase, ecto gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 62249 Nt5e 5' nucleotidase, ecto gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 62249 Nt5e 5' nucleotidase, ecto gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 62249 Nt5e 5' nucleotidase, ecto gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 62249 Nt5e 5' nucleotidase, ecto gene MP:0001357 increased aggression towards humans IAGP N RGD:5509061 20141003 MGI PMID:15583013 62249 Nt5e 5' nucleotidase, ecto gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15583013 62249 Nt5e 5' nucleotidase, ecto gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 62249 Nt5e 5' nucleotidase, ecto gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 62249 Nt5e 5' nucleotidase, ecto gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 62249 Nt5e 5' nucleotidase, ecto gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:15343381 62249 Nt5e 5' nucleotidase, ecto gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 62249 Nt5e 5' nucleotidase, ecto gene MP:0003023 decreased coronary flow rate IAGP N RGD:5509061 20141003 MGI PMID:15358667 62249 Nt5e 5' nucleotidase, ecto gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:17353435 62249 Nt5e 5' nucleotidase, ecto gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230119 MGI 62249 Nt5e 5' nucleotidase, ecto gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:15583013 62249 Nt5e 5' nucleotidase, ecto gene MP:0003195 calcinosis IAGP N RGD:5509061 20181122 MGI PMID:28592560 62249 Nt5e 5' nucleotidase, ecto gene MP:0003196 calcified skin IAGP N RGD:5509061 20181122 MGI PMID:28592560 62249 Nt5e 5' nucleotidase, ecto gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:15343381 62249 Nt5e 5' nucleotidase, ecto gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17353435 62249 Nt5e 5' nucleotidase, ecto gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:15583013 62249 Nt5e 5' nucleotidase, ecto gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:15358667 62249 Nt5e 5' nucleotidase, ecto gene MP:0005529 abnormal renal vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:15343381 62249 Nt5e 5' nucleotidase, ecto gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:15358667 62249 Nt5e 5' nucleotidase, ecto gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20230119 MGI 62249 Nt5e 5' nucleotidase, ecto gene MP:0030533 abnormal snout skin morphology IAGP N RGD:5509061 20181122 MGI PMID:28592560 62249 Nt5e 5' nucleotidase, ecto gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:15358667 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:21936904 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000265 blood vessel atresia IAGP N RGD:5509061 20141003 MGI PMID:23873040 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:14667410 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:21185281 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20231116 MGI PMID:33899511 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:14667410 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20161229 MGI PMID:25953344 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20141003 MGI PMID:22992950 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:22992950 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20220714 MGI PMID:34615475 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231116 MGI PMID:33899511 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231214 MGI PMID:23437302 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16556916 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:22345400 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20150716 MGI PMID:23028455 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:16556916 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:22438573 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000564 syndactyly IAGP N RGD:5509061 20221020 MGI PMID:32692983 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23790753 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:18849985 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8565076 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:16781703 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:18329011 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:16781703 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15836427 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18849985 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15836427 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18849985 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15836427 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:18849985 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:23790753 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000982 abnormal Meissner's corpuscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22345400 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0000988 abnormal pacinian corpuscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22345400 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001070 abnormal abducens nerve morphology IAGP N RGD:5509061 20200507 MGI PMID:28346224 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001086 absent petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:20133851 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18849985 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:12495620 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22345400 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19940179 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:18460603 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18460603 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:18434421 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22345400 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001575 cyanosis IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8565076 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:14667410 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18849985 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:8565076 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001787 pericardial edema IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20220714 MGI PMID:34615475 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:21936904 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:9000074 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16687132 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16741123 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:23873040 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17258700 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17626887 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20200507 MGI PMID:28346224 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20150716 MGI PMID:23028455 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22345400 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16556916 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16687132 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16720879 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:18832392 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:22992950 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:23873040 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20221020 MGI PMID:32692983 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002652 thin myocardium IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20231214 MGI PMID:23437302 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20231214 MGI PMID:23437302 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002748 abnormal pulmonary valve morphology IAGP N RGD:5509061 20231116 MGI PMID:33899511 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002748 abnormal pulmonary valve morphology IAGP N RGD:5509061 20231214 MGI PMID:23437302 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:14667410 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20220714 MGI PMID:34615475 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:14667410 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003126 abnormal external female genitalia morphology IAGP N RGD:5509061 20150716 MGI PMID:23028455 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003221 abnormal cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16556916 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003445 sirenomelia IAGP N RGD:5509061 20150716 MGI PMID:23028455 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20150716 MGI PMID:23028455 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16556916 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:23790753 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18460603 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003740 fusion of middle ear ossicles IAGP N RGD:5509061 20141003 MGI PMID:21936904 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:22438573 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003872 absent heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:14667410 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003872 absent heart right ventricle IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16720879 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23873040 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20161229 MGI PMID:25953344 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:12495620 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20240314 MGI PMID:32170006 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004100 abnormal spinal cord interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8565076 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20240314 MGI PMID:32170006 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004103 abnormal ventral striatum morphology IAGP N RGD:5509061 20240314 MGI PMID:32170006 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:16687132 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16687132 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20221020 MGI PMID:32692983 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20220714 MGI PMID:34615475 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:16687132 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20231214 MGI PMID:23437302 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:14667410 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004267 abnormal optic tract morphology IAGP N RGD:5509061 20141003 MGI PMID:18434421 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12495620 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12741988 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23790753 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004507 abnormal ischium morphology IAGP N RGD:5509061 20141003 MGI PMID:22438573 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004691 absent pubis IAGP N RGD:5509061 20141003 MGI PMID:22438573 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20161229 MGI PMID:25953344 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:8565076 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19940179 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0005156 bradykinesia IAGP N RGD:5509061 20220421 MGI PMID:23790753 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:9000074 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0005382 craniofacial phenotype IAGP N RGD:5509061 20220714 MGI PMID:34615475 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22345400 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:16741123 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:22345400 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006018 abnormal tympanic membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:21936904 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16720879 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21185281 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8565076 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18460603 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:16687132 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:18832392 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:21185281 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:22992950 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231116 MGI PMID:33899511 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231214 MGI PMID:23437302 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20221020 MGI PMID:32692983 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20141003 MGI PMID:18460603 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18434421 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23790753 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20150716 MGI PMID:23028455 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:18460603 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:21936904 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:16720879 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16687132 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:21936904 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0006408 dorsal root ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18849985 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18460603 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18434421 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:18460603 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0008314 abnormal pterygopalatine ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20133851 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0008486 decreased muscle spindle number IAGP N RGD:5509061 20141003 MGI PMID:15836427 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:18460603 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:18460603 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0008532 decreased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:18849985 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:22345400 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:18832392 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0009052 anal stenosis IAGP N RGD:5509061 20150716 MGI PMID:23028455 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9000074 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0009178 absent pancreatic alpha cells IAGP N RGD:5509061 20141003 MGI PMID:9000074 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0009203 external male genitalia hypoplasia IAGP N RGD:5509061 20150716 MGI PMID:23028455 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0009252 absent urinary bladder IAGP N RGD:5509061 20150716 MGI PMID:23028455 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:23790753 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20220714 MGI PMID:34615475 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0009913 abnormal hyoid bone greater horn morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19940179 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23790753 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16687132 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20220714 MGI PMID:34615475 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231116 MGI PMID:33899511 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231214 MGI PMID:23437302 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:16687132 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:22992950 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:22992950 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20221020 MGI PMID:32692983 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21185281 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20161229 MGI PMID:25953344 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:16720879 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20220714 MGI PMID:34615475 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:18832392 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0010602 abnormal pulmonary valve cusp morphology IAGP N RGD:5509061 20231214 MGI PMID:23437302 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19940179 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18849985 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20220714 MGI PMID:34615475 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23790753 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18849985 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21936904 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14667410 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16556916 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18849985 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21185281 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8565076 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20150716 MGI PMID:25053429 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20161229 MGI PMID:25953344 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18460603 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:32692983 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16720879 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20221020 MGI PMID:32692983 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011265 abnormal pancreas mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:9000074 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:23437302 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011851 abnormal embryonic cloaca development IAGP N RGD:5509061 20150716 MGI PMID:23028455 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21936904 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0012179 abnormal splanchnic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:14667410 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:8565076 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:16687132 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0013167 abnormal hindlimb bud morphology IAGP N RGD:5509061 20150528 MGI PMID:22438573 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0013167 abnormal hindlimb bud morphology IAGP N RGD:5509061 20150716 MGI PMID:23028455 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0013167 abnormal hindlimb bud morphology IAGP N RGD:5509061 20231130 MGI PMID:16556916 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0013169 small hindlimb buds IAGP N RGD:5509061 20231130 MGI PMID:16556916 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:8565076 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0013349 small Rathke's pouch IAGP N RGD:5509061 20141218 MGI PMID:9806931 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:9806931 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0014044 absent cardiac outflow tract IAGP N RGD:5509061 20160304 MGI PMID:14667410 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:23790753 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:22438573 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:18460603 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0030160 abnormal auditory bulla morphology IAGP N RGD:5509061 20171207 MGI PMID:21936904 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0030410 middle ear effusion IAGP N RGD:5509061 20171207 MGI PMID:21936904 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0030419 excessive cerumen IAGP N RGD:5509061 20171207 MGI PMID:21936904 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0030870 abnormal superior horn of thyroid cartilage morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0030871 abnormal inferior horn of thyroid cartilage morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0030996 decreased pacinian corpuscle number IAGP N RGD:5509061 20200130 MGI PMID:22345400 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0030998 small pacinian corpuscles IAGP N RGD:5509061 20200130 MGI PMID:22345400 62250 Isl1 ISL1 transcription factor, LIM/homeodomain gene MP:0031581 semilunar valve hyperplasia IAGP N RGD:5509061 20240125 MGI PMID:23437302 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15138255 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0000262 poor arterial differentiation IAGP N RGD:5509061 20141003 MGI PMID:12869509 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:22975327 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:11032855 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16314531 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:16314531 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:16314531 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:21177428 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12869509 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11032855 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:11032855 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:12869509 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:11032855 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:11032855 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11032855 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12869509 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15138255 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16314531 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:11032855 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:12869509 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:15138255 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:12869509 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12869509 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:22975327 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21960637 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22975327 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:20584883 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22975327 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:22975327 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21177428 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11032855 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11032855 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20584883 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21177428 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21960637 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:21177428 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:11032855 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11032855 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19808259 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19808259 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20584883 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20584883 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20584883 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0009864 abnormal aorta endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22975327 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15138255 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22975327 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15138255 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22975327 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11032855 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12869509 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15138255 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0011707 impaired fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:11032855 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:12869509 62251 S1pr1 sphingosine-1-phosphate receptor 1 gene MP:0020321 increased vascular endothelial cell apoptosis IAGP N RGD:5509061 20160616 MGI PMID:22975327 62252 Txnrd1 thioredoxin reductase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15713651 62252 Txnrd1 thioredoxin reductase 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:17697936 62252 Txnrd1 thioredoxin reductase 1 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:17697936 62252 Txnrd1 thioredoxin reductase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15713651 62252 Txnrd1 thioredoxin reductase 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:15713651 62252 Txnrd1 thioredoxin reductase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15713651 62252 Txnrd1 thioredoxin reductase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17697936 62252 Txnrd1 thioredoxin reductase 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20160331 MGI PMID:17697936 62252 Txnrd1 thioredoxin reductase 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15713651 62252 Txnrd1 thioredoxin reductase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17697936 62252 Txnrd1 thioredoxin reductase 1 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15713651 62252 Txnrd1 thioredoxin reductase 1 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18350150 62252 Txnrd1 thioredoxin reductase 1 gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:17697936 62252 Txnrd1 thioredoxin reductase 1 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:15713651 62252 Txnrd1 thioredoxin reductase 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17697936 62252 Txnrd1 thioredoxin reductase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15713651 62252 Txnrd1 thioredoxin reductase 1 gene MP:0011184 absent embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:17697936 62252 Txnrd1 thioredoxin reductase 1 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:17697936 62252 Txnrd1 thioredoxin reductase 1 gene MP:0011705 absent fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:15713651 62252 Txnrd1 thioredoxin reductase 1 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:15713651 62253 Txnrd2 thioredoxin reductase 2 gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18350150 62253 Txnrd2 thioredoxin reductase 2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:15485910 62253 Txnrd2 thioredoxin reductase 2 gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:15485910 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15138255 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:12006579 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:15138255 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15138255 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15138255 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11443127 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12006579 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:15138255 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160128 MGI PMID:26494861 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15968000 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15184895 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:17284444 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0004331 vestibular saccular macula degeneration IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0004334 utricular macular degeneration IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0004518 absent vestibular hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:17284444 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11443127 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15138255 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17287522 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18305483 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18305483 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:18305483 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18305483 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20190502 MGI 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12006579 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15138255 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17284444 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15138255 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 62254 S1pr3 sphingosine-1-phosphate receptor 3 gene MP:0031434 increased miscarriage rate IAGP N RGD:5509061 20220915 MGI PMID:15138255 62255 Cryba4 crystallin, beta A4 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 62256 Fhl2 four and a half LIM domains 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16079911 62256 Fhl2 four and a half LIM domains 2 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:16079911 62256 Fhl2 four and a half LIM domains 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11390345 62256 Fhl2 four and a half LIM domains 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:23271052 62256 Fhl2 four and a half LIM domains 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11003643 62256 Fhl2 four and a half LIM domains 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23271052 62256 Fhl2 four and a half LIM domains 2 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:16079911 62257 Gstm5 glutathione S-transferase, mu 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 62257 Gstm5 glutathione S-transferase, mu 5 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20210520 MGI 62257 Gstm5 glutathione S-transferase, mu 5 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16845389 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0000683 decreased percent water in carcass IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22000926 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14693698 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16845389 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22000926 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22000926 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:14693698 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:16845389 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22000926 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14693698 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10066179 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16845389 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:10066179 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:14693698 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16845389 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:22000926 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:16845389 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22000926 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:22000926 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14693698 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:16845389 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22000926 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:10066179 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16845389 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:14693698 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10066179 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16845389 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16845389 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005451 abnormal body composition IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18719666 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:14693698 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10066179 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16845389 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22000926 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:10066179 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22000926 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22000926 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16845389 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20191212 MGI PMID:27020859 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20191212 MGI PMID:27020859 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:16845389 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0011016 increased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:10891488 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:16845389 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0014440 increased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:16845389 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0014440 increased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:22000926 62258 Ptpn1 protein tyrosine phosphatase, non-receptor type 1 gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:16845389 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230119 MGI 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0000243 myoclonus IAGP N RGD:5509061 20210902 MGI PMID:33582225 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17947380 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20230119 MGI 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15850489 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23457547 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:7644489 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:14572465 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17572671 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17947380 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:7644489 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:23457547 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:23457547 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:7644489 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:23457547 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:7644489 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23457547 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10218866 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:14572465 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002064 seizures IAGP N RGD:5509061 20210902 MGI PMID:33582225 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14572465 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14572465 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20210902 MGI PMID:33582225 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20210902 MGI PMID:33582225 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20230119 MGI 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:23196213 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:17947380 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:18825662 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20210902 MGI PMID:33582225 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17572671 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17947380 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22993424 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23457547 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:17947380 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0003216 absence seizures IAGP N RGD:5509061 20210902 MGI PMID:33582225 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20210902 MGI PMID:33582225 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:10218866 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:22993424 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22993424 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:17947380 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:19903874 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20210401 MGI PMID:32853550 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15165831 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:10880692 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19903874 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:19903874 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10880692 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15165831 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17572671 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20240523 MGI 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23457547 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15850489 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17947380 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7644489 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17947380 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19903874 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0012011 febrile seizures IAGP N RGD:5509061 20210902 MGI PMID:33582225 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:19903874 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0014384 increased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:19903874 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:33582225 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0031185 sudden unexpected death in epilepsy IAGP N RGD:5509061 20210902 MGI PMID:33582225 62259 Gabrg2 gamma-aminobutyric acid type A receptor, subunit gamma 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:33582225 62260 Mcm6 minichromosome maintenance complex component 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20838603 62260 Mcm6 minichromosome maintenance complex component 6 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20838603 62260 Mcm6 minichromosome maintenance complex component 6 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20838603 62260 Mcm6 minichromosome maintenance complex component 6 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:20838603 62260 Mcm6 minichromosome maintenance complex component 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20838603 62260 Mcm6 minichromosome maintenance complex component 6 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20838603 62260 Mcm6 minichromosome maintenance complex component 6 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20838603 62260 Mcm6 minichromosome maintenance complex component 6 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20838603 62261 Kcnj2 potassium inwardly-rectifying channel, subfamily J, member 2 gene MP:0001429 dehydration IAGP N RGD:5509061 20171019 MGI PMID:10904001 62261 Kcnj2 potassium inwardly-rectifying channel, subfamily J, member 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20171019 MGI PMID:10904001 62261 Kcnj2 potassium inwardly-rectifying channel, subfamily J, member 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10904001 62261 Kcnj2 potassium inwardly-rectifying channel, subfamily J, member 2 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:10904001 62261 Kcnj2 potassium inwardly-rectifying channel, subfamily J, member 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10904001 62261 Kcnj2 potassium inwardly-rectifying channel, subfamily J, member 2 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20221208 MGI PMID:22949619 62261 Kcnj2 potassium inwardly-rectifying channel, subfamily J, member 2 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20221208 MGI PMID:22949619 62261 Kcnj2 potassium inwardly-rectifying channel, subfamily J, member 2 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20221208 MGI PMID:22949619 62261 Kcnj2 potassium inwardly-rectifying channel, subfamily J, member 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:10904001 62261 Kcnj2 potassium inwardly-rectifying channel, subfamily J, member 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:10904001 62261 Kcnj2 potassium inwardly-rectifying channel, subfamily J, member 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221208 MGI PMID:22949619 62261 Kcnj2 potassium inwardly-rectifying channel, subfamily J, member 2 gene MP:0009897 decreased maxillary shelf size IAGP N RGD:5509061 20221208 MGI PMID:22949619 62261 Kcnj2 potassium inwardly-rectifying channel, subfamily J, member 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10904001 62261 Kcnj2 potassium inwardly-rectifying channel, subfamily J, member 2 gene MP:0030248 narrow maxilla IAGP N RGD:5509061 20171019 MGI PMID:10904001 62261 Kcnj2 potassium inwardly-rectifying channel, subfamily J, member 2 gene MP:0030266 small vomer bone IAGP N RGD:5509061 20221208 MGI PMID:22949619 62262 Hpse heparanase gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20150226 MGI PMID:24532362 62262 Hpse heparanase gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:19360105 62262 Hpse heparanase gene MP:0003711 pathological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:19360105 62262 Hpse heparanase gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20150226 MGI PMID:24532362 62262 Hpse heparanase gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20150226 MGI PMID:24532362 62262 Hpse heparanase gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 62262 Hpse heparanase gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19360105 62262 Hpse heparanase gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19360105 62262 Hpse heparanase gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20150226 MGI PMID:24532362 62262 Hpse heparanase gene MP:0008117 abnormal Langerhans cell morphology IAGP N RGD:5509061 20150226 MGI PMID:24532362 62262 Hpse heparanase gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20150226 MGI PMID:24532362 62262 Hpse heparanase gene MP:0010740 abnormal dendritic cell chemotaxis IAGP N RGD:5509061 20150226 MGI PMID:24532362 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20200402 MGI 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200402 MGI 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0000692 small spleen IEA N RGD:5509061 20200402 MGI 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20200402 MGI 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20180510 MGI PMID:27666520 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0001147 small testis IAGP N RGD:5509061 20180510 MGI PMID:27666520 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20180510 MGI PMID:27666520 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20181227 MGI 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20180510 MGI PMID:27666520 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0001925 male infertility IAGP N RGD:5509061 20180510 MGI PMID:27666520 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20200402 MGI 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20180510 MGI PMID:27666520 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0002989 small kidney IEA N RGD:5509061 20200402 MGI 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180510 MGI PMID:27666520 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20180510 MGI PMID:27666520 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20180510 MGI PMID:27666520 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180510 MGI PMID:27666520 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180510 MGI PMID:27666520 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180510 MGI PMID:27666520 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20200402 MGI 62263 Ptp4a1 protein tyrosine phosphatase 4a1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20180510 MGI PMID:27666520 62264 Kcnj5 potassium inwardly-rectifying channel, subfamily J, member 5 gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:9459446 62264 Kcnj5 potassium inwardly-rectifying channel, subfamily J, member 5 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20170223 MGI PMID:26831068 62265 Slc15a2 solute carrier family 15 (H+/peptide transporter), member 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12473671 62265 Slc15a2 solute carrier family 15 (H+/peptide transporter), member 2 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:12697824 62265 Slc15a2 solute carrier family 15 (H+/peptide transporter), member 2 gene MP:0011445 abnormal renal protein reabsorption IAGP N RGD:5509061 20141003 MGI PMID:12697824 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19351902 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:19351902 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19351902 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18701065 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19351902 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:18701065 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:19351902 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19351902 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19351902 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:21924222 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:21924222 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18701065 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21924222 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:21261756 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:21924222 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19351902 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62266 Trpc3 transient receptor potential cation channel, subfamily C, member 3 gene MP:0011176 abnormal erythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:21924222 62267 Hpd 4-hydroxyphenylpyruvic acid dioxygenase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:2014797 62267 Hpd 4-hydroxyphenylpyruvic acid dioxygenase gene MP:0013724 decreased circulating tyrosine level IAGP N RGD:5509061 20150409 MGI PMID:2014797 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:15639173 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15639173 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:14977190 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:14977190 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:15639173 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:14977190 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15639173 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:14977190 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15639173 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15639173 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:14977190 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:15639173 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:14977190 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15639173 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:14977190 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20141003 MGI PMID:14977190 62269 Ckmt1 creatine kinase, mitochondrial 1, ubiquitous gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:15639173 62270 Klrg1 killer cell lectin-like receptor subfamily G, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20201037 62271 Eef2 eukaryotic translation elongation factor 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:22869748 62271 Eef2 eukaryotic translation elongation factor 2 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22869748 62271 Eef2 eukaryotic translation elongation factor 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22869748 62271 Eef2 eukaryotic translation elongation factor 2 gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:22869748 62271 Eef2 eukaryotic translation elongation factor 2 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:22869748 62271 Eef2 eukaryotic translation elongation factor 2 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22869748 62271 Eef2 eukaryotic translation elongation factor 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22869748 62272 Crybb3 crystallin, beta B3 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20181227 MGI 62272 Crybb3 crystallin, beta B3 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20181227 MGI 62273 Csn2 casein beta gene MP:0003718 maternal effect IAGP N RGD:5509061 20180719 MGI PMID:8016126 62273 Csn2 casein beta gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20180719 MGI PMID:8016126 62274 Hpn hepsin gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22912808 62274 Hpn hepsin gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:17620368 62274 Hpn hepsin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22912808 62274 Hpn hepsin gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22912808 62274 Hpn hepsin gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17620368 62274 Hpn hepsin gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:22912808 62274 Hpn hepsin gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:9435303 62274 Hpn hepsin gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17620368 62274 Hpn hepsin gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:17620368 62274 Hpn hepsin gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17620368 62274 Hpn hepsin gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17620368 62274 Hpn hepsin gene MP:0004591 enlarged tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:17620368 62274 Hpn hepsin gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20141003 MGI 62274 Hpn hepsin gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22912808 62274 Hpn hepsin gene MP:0005471 decreased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:17620368 62274 Hpn hepsin gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:17620368 62274 Hpn hepsin gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:22912808 62274 Hpn hepsin gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:17620368 62274 Hpn hepsin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17620368 62274 Hpn hepsin gene MP:0014091 abnormal tectorial membrane striated-sheet matrix morphology IAGP N RGD:5509061 20160421 MGI PMID:17620368 62275 Grn granulin gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20220616 MGI PMID:34130995 62275 Grn granulin gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:22733568 62275 Grn granulin gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22733568 62275 Grn granulin gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 62275 Grn granulin gene MP:0000798 abnormal frontal lobe morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 62275 Grn granulin gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 62275 Grn granulin gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 62275 Grn granulin gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 62275 Grn granulin gene MP:0001212 skin lesions IAGP N RGD:5509061 20190627 MGI PMID:29511098 62275 Grn granulin gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0001260 increased body weight IAGP N RGD:5509061 20220616 MGI PMID:34130995 62275 Grn granulin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20181004 MGI PMID:29382817 62275 Grn granulin gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:17764761 62275 Grn granulin gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:22062772 62275 Grn granulin gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17764761 62275 Grn granulin gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20220616 MGI PMID:34130995 62275 Grn granulin gene MP:0001378 abnormal ejaculation IAGP N RGD:5509061 20141003 MGI PMID:17764761 62275 Grn granulin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22062772 62275 Grn granulin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20181004 MGI PMID:29382817 62275 Grn granulin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20220616 MGI PMID:34130995 62275 Grn granulin gene MP:0001426 polydipsia IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20190627 MGI PMID:29511098 62275 Grn granulin gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:22733568 62275 Grn granulin gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:22733568 62275 Grn granulin gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22062772 62275 Grn granulin gene MP:0001752 abnormal hypothalamus secretion IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0001762 polyuria IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:22062772 62275 Grn granulin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22733568 62275 Grn granulin gene MP:0002083 premature death IAGP N RGD:5509061 20190627 MGI PMID:29511098 62275 Grn granulin gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:22733568 62275 Grn granulin gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20181004 MGI PMID:29382817 62275 Grn granulin gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20151001 MGI PMID:25155018 62275 Grn granulin gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20026663 62275 Grn granulin gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20026663 62275 Grn granulin gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:21368173 62275 Grn granulin gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20190627 MGI PMID:29511098 62275 Grn granulin gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 62275 Grn granulin gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:22062772 62275 Grn granulin gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:22062772 62275 Grn granulin gene MP:0002981 increased liver weight IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:23041626 62275 Grn granulin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:20026663 62275 Grn granulin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22062772 62275 Grn granulin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22733568 62275 Grn granulin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:22062772 62275 Grn granulin gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:22733568 62275 Grn granulin gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20026663 62275 Grn granulin gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:22062772 62275 Grn granulin gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20151001 MGI PMID:25155018 62275 Grn granulin gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20220616 MGI PMID:34130995 62275 Grn granulin gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20181004 MGI PMID:29382817 62275 Grn granulin gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:23041626 62275 Grn granulin gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20151001 MGI PMID:25155018 62275 Grn granulin gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:20026663 62275 Grn granulin gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0005610 increased circulating antidiuretic hormone level IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20151001 MGI PMID:25155018 62275 Grn granulin gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20151001 MGI PMID:25155018 62275 Grn granulin gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20151001 MGI PMID:25155018 62275 Grn granulin gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22062772 62275 Grn granulin gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:22062772 62275 Grn granulin gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20181004 MGI PMID:29382817 62275 Grn granulin gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20026663 62275 Grn granulin gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23041626 62275 Grn granulin gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:23041626 62275 Grn granulin gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:23041626 62275 Grn granulin gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:20026663 62275 Grn granulin gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20026663 62275 Grn granulin gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:23041626 62275 Grn granulin gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20026663 62275 Grn granulin gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20190627 MGI PMID:29511098 62275 Grn granulin gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20141003 MGI PMID:22062772 62275 Grn granulin gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20190627 MGI PMID:29511098 62275 Grn granulin gene MP:0008845 abnormal paraventricular hypothalamic nucleus morphology IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0008846 abnormal supraoptic nucleus morphology IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:20026663 62275 Grn granulin gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:22062772 62275 Grn granulin gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:22733568 62275 Grn granulin gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23041626 62275 Grn granulin gene MP:0008918 microgliosis IAGP N RGD:5509061 20190627 MGI PMID:29511098 62275 Grn granulin gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:22733568 62275 Grn granulin gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 62275 Grn granulin gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20181004 MGI PMID:29382817 62275 Grn granulin gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20190627 MGI PMID:29511098 62275 Grn granulin gene MP:0009615 abnormal zinc homeostasis IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22733568 62275 Grn granulin gene MP:0010369 abnormal thalamus neuron morphology IAGP N RGD:5509061 20190627 MGI PMID:29511098 62275 Grn granulin gene MP:0011436 decreased urine magnesium level IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0011444 abnormal renal water homeostasis IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:23041626 62275 Grn granulin gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0011612 increased circulating ghrelin level IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0011939 increased food intake IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20190307 MGI PMID:30271659 62275 Grn granulin gene MP:0011975 neuronal cytoplasmic inclusions IAGP N RGD:5509061 20181004 MGI PMID:29382817 62275 Grn granulin gene MP:0011975 neuronal cytoplasmic inclusions IAGP N RGD:5509061 20190627 MGI PMID:29511098 62275 Grn granulin gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20151001 MGI PMID:25155018 62275 Grn granulin gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20151001 MGI PMID:25155018 62275 Grn granulin gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20220616 MGI PMID:34130995 62275 Grn granulin gene MP:0012448 abnormal primary motor cortex morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 62275 Grn granulin gene MP:0012489 abnormal retrosplenial region morphology IAGP N RGD:5509061 20220616 MGI PMID:34130995 62275 Grn granulin gene MP:0014062 nervous system inclusion bodies IAGP N RGD:5509061 20181004 MGI PMID:29382817 62275 Grn granulin gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20170803 MGI PMID:22733568 62275 Grn granulin gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20181004 MGI PMID:29382817 62275 Grn granulin gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20211014 MGI PMID:22062772 62276 Dmbt1 deleted in malignant brain tumors 1 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21098262 62276 Dmbt1 deleted in malignant brain tumors 1 gene MP:0000525 renal tubular acidosis IAGP N RGD:5509061 20141003 MGI PMID:21098262 62276 Dmbt1 deleted in malignant brain tumors 1 gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20141003 MGI PMID:15452149 62276 Dmbt1 deleted in malignant brain tumors 1 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:15452149 62276 Dmbt1 deleted in malignant brain tumors 1 gene MP:0003017 decreased circulating bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:21098262 62276 Dmbt1 deleted in malignant brain tumors 1 gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:15452149 62276 Dmbt1 deleted in malignant brain tumors 1 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:15452149 62276 Dmbt1 deleted in malignant brain tumors 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:17983803 62276 Dmbt1 deleted in malignant brain tumors 1 gene MP:0009349 increased urine pH IAGP N RGD:5509061 20141003 MGI PMID:21098262 62276 Dmbt1 deleted in malignant brain tumors 1 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15452149 62276 Dmbt1 deleted in malignant brain tumors 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15452149 62276 Dmbt1 deleted in malignant brain tumors 1 gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20170921 MGI PMID:21098262 62276 Dmbt1 deleted in malignant brain tumors 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:18202109 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0000622 increased salivation IAGP N RGD:5509061 20141003 MGI PMID:10624964 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10624964 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10624964 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:22859683 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:14565944 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:10624964 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:10624964 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:22859683 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:10624964 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14565944 62277 Grk5 G protein-coupled receptor kinase 5 gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:10624964 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20151119 MGI PMID:23443560 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20151119 MGI PMID:23443560 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12032308 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12032308 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20151119 MGI PMID:23443560 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20151119 MGI PMID:23443560 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20151119 MGI PMID:23443560 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20151119 MGI PMID:23443560 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20151119 MGI PMID:23443560 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20151119 MGI PMID:23443560 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20151119 MGI PMID:23443560 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20151119 MGI PMID:23443560 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20151119 MGI PMID:23443560 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20151119 MGI PMID:23443560 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:12718862 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:12718862 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0009754 enhanced behavioral response to cocaine IMP N RGD:5684935|PMID:12718862 20120105 RGD 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20151119 MGI PMID:23443560 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IAGP N RGD:5509061 20151119 MGI PMID:23443560 62278 Grk6 G protein-coupled receptor kinase 6 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:12718862 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:20966073 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:14645240 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:14645240 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14645240 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20966073 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:14645240 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20200402 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:14645240 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:14645240 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:14645240 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20200402 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20210520 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200402 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14645240 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20200402 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20200402 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0002080 prenatal lethality IEA N RGD:5509061 20201231 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200402 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:20966073 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20200402 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:14645240 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:14645240 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:14645240 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:14645240 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:14645240 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20210128 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14645240 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0011495 abnormal head shape IEA N RGD:5509061 20200402 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0011496 abnormal head size IEA N RGD:5509061 20200402 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0011940 decreased food intake IEA N RGD:5509061 20210128 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0011942 decreased fluid intake IEA N RGD:5509061 20210128 MGI 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0030655 increased circulating glycine level IAGP N RGD:5509061 20180913 MGI PMID:20966073 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0030659 decreased glycine level IAGP N RGD:5509061 20180927 MGI PMID:20966073 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0030664 increased arginine level IAGP N RGD:5509061 20180927 MGI PMID:20966073 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0030665 decreased arginine level IAGP N RGD:5509061 20180927 MGI PMID:20966073 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0030685 decreased cystathionine level IAGP N RGD:5509061 20180927 MGI PMID:20966073 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0030692 decreased serine level IAGP N RGD:5509061 20180927 MGI PMID:20966073 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0030697 increased phenylalanine level IAGP N RGD:5509061 20180927 MGI PMID:20966073 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0030698 decreased phenylalanine level IAGP N RGD:5509061 20180927 MGI PMID:20966073 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0030701 decreased threonine level IAGP N RGD:5509061 20180927 MGI PMID:20966073 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0030706 increased glutamine level IAGP N RGD:5509061 20180927 MGI PMID:20966073 62279 Phgdh 3-phosphoglycerate dehydrogenase gene MP:0030737 decreased glutamic acid level IAGP N RGD:5509061 20180927 MGI PMID:20966073 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11668343 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20190418 MGI PMID:29233179 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0002367 abnormal thymus lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:11668343 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11668343 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:11668343 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0002434 abnormal T-helper 2 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15699073 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:15699073 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11668343 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11668343 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0009710 anhedonia IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20190418 MGI PMID:29233179 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20190418 MGI PMID:29233179 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0013593 enlarged thymus cortex IAGP N RGD:5509061 20150326 MGI PMID:11668343 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0020335 abnormal dentate gyrus neuron dendrite morphology IAGP N RGD:5509061 20190418 MGI PMID:29233179 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20180802 MGI PMID:23389689 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0020510 increased dendritic spine length IAGP N RGD:5509061 20190418 MGI PMID:29233179 62280 Hivep2 human immunodeficiency virus type I enhancer binding protein 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:27028761 62281 Ankrd1 ankyrin repeat domain 1 gene MP:0001220 epidermal necrosis IAGP N RGD:5509061 20160225 MGI PMID:25452119 62281 Ankrd1 ankyrin repeat domain 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 62281 Ankrd1 ankyrin repeat domain 1 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20160225 MGI PMID:25452119 62281 Ankrd1 ankyrin repeat domain 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20160225 MGI PMID:25452119 62281 Ankrd1 ankyrin repeat domain 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:17392382 62281 Ankrd1 ankyrin repeat domain 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141225 MGI PMID:24736439 62281 Ankrd1 ankyrin repeat domain 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160225 MGI PMID:25452119 62281 Ankrd1 ankyrin repeat domain 1 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20160225 MGI PMID:25452119 62281 Ankrd1 ankyrin repeat domain 1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:17392382 62281 Ankrd1 ankyrin repeat domain 1 gene MP:0012688 abnormal heart ventricles weight IAGP N RGD:5509061 20160225 MGI PMID:25452119 62282 Csn3 casein kappa gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:16698927 62282 Csn3 casein kappa gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:16698927 62283 Smc1a structural maintenance of chromosomes 1A gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:15175241 62283 Smc1a structural maintenance of chromosomes 1A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16357220 62283 Smc1a structural maintenance of chromosomes 1A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16357220 62283 Smc1a structural maintenance of chromosomes 1A gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16357220 62283 Smc1a structural maintenance of chromosomes 1A gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16357220 62283 Smc1a structural maintenance of chromosomes 1A gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:15175241 62283 Smc1a structural maintenance of chromosomes 1A gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:15175241 62283 Smc1a structural maintenance of chromosomes 1A gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:15175241 62283 Smc1a structural maintenance of chromosomes 1A gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16357220 62283 Smc1a structural maintenance of chromosomes 1A gene MP:0005432 abnormal pro-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16357220 62283 Smc1a structural maintenance of chromosomes 1A gene MP:0008404 increased cellular sensitivity to methylmethanesulfonate IAGP N RGD:5509061 20141003 MGI PMID:15175241 62285 Plcb3 phospholipase C, beta 3 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:10669417 62285 Plcb3 phospholipase C, beta 3 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9883896 62285 Plcb3 phospholipase C, beta 3 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:10669417 62285 Plcb3 phospholipase C, beta 3 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:10669417 62285 Plcb3 phospholipase C, beta 3 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:9883896 62285 Plcb3 phospholipase C, beta 3 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11145744 62285 Plcb3 phospholipase C, beta 3 gene MP:0004270 analgesia IAGP N RGD:5509061 20141003 MGI PMID:10468617 62285 Plcb3 phospholipase C, beta 3 gene MP:0004867 decreased platelet calcium level IAGP N RGD:5509061 20141003 MGI PMID:10669417 62285 Plcb3 phospholipase C, beta 3 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:10669417 62285 Plcb3 phospholipase C, beta 3 gene MP:0009449 increased platelet ATP level IAGP N RGD:5509061 20141003 MGI PMID:10669417 62285 Plcb3 phospholipase C, beta 3 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:10669417 62285 Plcb3 phospholipase C, beta 3 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9883896 62285 Plcb3 phospholipase C, beta 3 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201002 MGI PMID:10669417 62287 Pten phosphatase and tensin homolog gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:16537919 62287 Pten phosphatase and tensin homolog gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:21266327 62287 Pten phosphatase and tensin homolog gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18687666 62287 Pten phosphatase and tensin homolog gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18463637 62287 Pten phosphatase and tensin homolog gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18463637 62287 Pten phosphatase and tensin homolog gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16598206 62287 Pten phosphatase and tensin homolog gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18687666 62287 Pten phosphatase and tensin homolog gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20151015 MGI PMID:25234167 62287 Pten phosphatase and tensin homolog gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:23023706 62287 Pten phosphatase and tensin homolog gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12297047 62287 Pten phosphatase and tensin homolog gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:12297047 62287 Pten phosphatase and tensin homolog gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16598206 62287 Pten phosphatase and tensin homolog gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:19038262 62287 Pten phosphatase and tensin homolog gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20150430 MGI PMID:24470394 62287 Pten phosphatase and tensin homolog gene MP:0000381 enlarged hair follicles IAGP N RGD:5509061 20181129 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16204035 62287 Pten phosphatase and tensin homolog gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:19011632 62287 Pten phosphatase and tensin homolog gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:11691952 62287 Pten phosphatase and tensin homolog gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:15944184 62287 Pten phosphatase and tensin homolog gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:19208814 62287 Pten phosphatase and tensin homolog gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:19470613 62287 Pten phosphatase and tensin homolog gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:21343951 62287 Pten phosphatase and tensin homolog gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:23475934 62287 Pten phosphatase and tensin homolog gene MP:0000434 megacephaly IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0000434 megacephaly IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19168705 62287 Pten phosphatase and tensin homolog gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19884655 62287 Pten phosphatase and tensin homolog gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19011632 62287 Pten phosphatase and tensin homolog gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19168705 62287 Pten phosphatase and tensin homolog gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:19168705 62287 Pten phosphatase and tensin homolog gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:16488991 62287 Pten phosphatase and tensin homolog gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:16488991 62287 Pten phosphatase and tensin homolog gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:16951148 62287 Pten phosphatase and tensin homolog gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:18497742 62287 Pten phosphatase and tensin homolog gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18497742 62287 Pten phosphatase and tensin homolog gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:18497742 62287 Pten phosphatase and tensin homolog gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:18497742 62287 Pten phosphatase and tensin homolog gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16488991 62287 Pten phosphatase and tensin homolog gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16951148 62287 Pten phosphatase and tensin homolog gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18497742 62287 Pten phosphatase and tensin homolog gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20818428 62287 Pten phosphatase and tensin homolog gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20160915 MGI PMID:21283818 62287 Pten phosphatase and tensin homolog gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17567478 62287 Pten phosphatase and tensin homolog gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20150709 MGI PMID:20837017 62287 Pten phosphatase and tensin homolog gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:14769918 62287 Pten phosphatase and tensin homolog gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:16767220 62287 Pten phosphatase and tensin homolog gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:17567478 62287 Pten phosphatase and tensin homolog gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:18463637 62287 Pten phosphatase and tensin homolog gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:21479224 62287 Pten phosphatase and tensin homolog gene MP:0000599 enlarged liver IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0000599 enlarged liver IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0000599 enlarged liver IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:14769918 62287 Pten phosphatase and tensin homolog gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:17567478 62287 Pten phosphatase and tensin homolog gene MP:0000603 pale liver IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17567478 62287 Pten phosphatase and tensin homolog gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0000611 jaundice IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:20592216 62287 Pten phosphatase and tensin homolog gene MP:0000621 increased salivary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11178110 62287 Pten phosphatase and tensin homolog gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12163417 62287 Pten phosphatase and tensin homolog gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:14522255 62287 Pten phosphatase and tensin homolog gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:14691534 62287 Pten phosphatase and tensin homolog gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15994948 62287 Pten phosphatase and tensin homolog gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18043744 62287 Pten phosphatase and tensin homolog gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19185849 62287 Pten phosphatase and tensin homolog gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:12163417 62287 Pten phosphatase and tensin homolog gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:21952241 62287 Pten phosphatase and tensin homolog gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:22167068 62287 Pten phosphatase and tensin homolog gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16818619 62287 Pten phosphatase and tensin homolog gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18463637 62287 Pten phosphatase and tensin homolog gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21262837 62287 Pten phosphatase and tensin homolog gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20151015 MGI PMID:25234167 62287 Pten phosphatase and tensin homolog gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16598206 62287 Pten phosphatase and tensin homolog gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18463637 62287 Pten phosphatase and tensin homolog gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:16598206 62287 Pten phosphatase and tensin homolog gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:18463637 62287 Pten phosphatase and tensin homolog gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:21262837 62287 Pten phosphatase and tensin homolog gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20151015 MGI PMID:25234167 62287 Pten phosphatase and tensin homolog gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:19176372 62287 Pten phosphatase and tensin homolog gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:18948956 62287 Pten phosphatase and tensin homolog gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:20592216 62287 Pten phosphatase and tensin homolog gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11691952 62287 Pten phosphatase and tensin homolog gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:16818619 62287 Pten phosphatase and tensin homolog gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:19211894 62287 Pten phosphatase and tensin homolog gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:11691952 62287 Pten phosphatase and tensin homolog gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:11691952 62287 Pten phosphatase and tensin homolog gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:15944184 62287 Pten phosphatase and tensin homolog gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:15944184 62287 Pten phosphatase and tensin homolog gene MP:0000858 abnormal metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16818619 62287 Pten phosphatase and tensin homolog gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:15944184 62287 Pten phosphatase and tensin homolog gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:15944184 62287 Pten phosphatase and tensin homolog gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15944184 62287 Pten phosphatase and tensin homolog gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:19750226 62287 Pten phosphatase and tensin homolog gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:9799734 62287 Pten phosphatase and tensin homolog gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:15492213 62287 Pten phosphatase and tensin homolog gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16818619 62287 Pten phosphatase and tensin homolog gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:16818619 62287 Pten phosphatase and tensin homolog gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20592216 62287 Pten phosphatase and tensin homolog gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:19884655 62287 Pten phosphatase and tensin homolog gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:19884655 62287 Pten phosphatase and tensin homolog gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19884655 62287 Pten phosphatase and tensin homolog gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20200123 MGI PMID:21576358 62287 Pten phosphatase and tensin homolog gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:23319880 62287 Pten phosphatase and tensin homolog gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20592216 62287 Pten phosphatase and tensin homolog gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:16818619 62287 Pten phosphatase and tensin homolog gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18239123 62287 Pten phosphatase and tensin homolog gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:22214849 62287 Pten phosphatase and tensin homolog gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:18239123 62287 Pten phosphatase and tensin homolog gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18239123 62287 Pten phosphatase and tensin homolog gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18606860 62287 Pten phosphatase and tensin homolog gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19843540 62287 Pten phosphatase and tensin homolog gene MP:0001133 impaired luteal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18606860 62287 Pten phosphatase and tensin homolog gene MP:0001138 abnormal uterine cervix squamous epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18474617 62287 Pten phosphatase and tensin homolog gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:19237610 62287 Pten phosphatase and tensin homolog gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:14691534 62287 Pten phosphatase and tensin homolog gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17607361 62287 Pten phosphatase and tensin homolog gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20160211 MGI PMID:22350410 62287 Pten phosphatase and tensin homolog gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20170323 MGI PMID:27345403 62287 Pten phosphatase and tensin homolog gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:14522255 62287 Pten phosphatase and tensin homolog gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:14691534 62287 Pten phosphatase and tensin homolog gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15994948 62287 Pten phosphatase and tensin homolog gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16079851 62287 Pten phosphatase and tensin homolog gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:16489020 62287 Pten phosphatase and tensin homolog gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11854455 62287 Pten phosphatase and tensin homolog gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14522255 62287 Pten phosphatase and tensin homolog gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14691534 62287 Pten phosphatase and tensin homolog gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19185849 62287 Pten phosphatase and tensin homolog gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20220303 MGI PMID:15994948 62287 Pten phosphatase and tensin homolog gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:19574443 62287 Pten phosphatase and tensin homolog gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:23023706 62287 Pten phosphatase and tensin homolog gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19574443 62287 Pten phosphatase and tensin homolog gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:23023706 62287 Pten phosphatase and tensin homolog gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:19884655 62287 Pten phosphatase and tensin homolog gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:23873941 62287 Pten phosphatase and tensin homolog gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:22796458 62287 Pten phosphatase and tensin homolog gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:23873941 62287 Pten phosphatase and tensin homolog gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23873941 62287 Pten phosphatase and tensin homolog gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:16204035 62287 Pten phosphatase and tensin homolog gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:23873941 62287 Pten phosphatase and tensin homolog gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16204035 62287 Pten phosphatase and tensin homolog gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23873941 62287 Pten phosphatase and tensin homolog gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:23873941 62287 Pten phosphatase and tensin homolog gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20852026 62287 Pten phosphatase and tensin homolog gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18281487 62287 Pten phosphatase and tensin homolog gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0001263 weight loss IAGP N RGD:5509061 20170601 MGI PMID:24512487 62287 Pten phosphatase and tensin homolog gene MP:0001263 weight loss IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17540362 62287 Pten phosphatase and tensin homolog gene MP:0001265 decreased body size IAGP N RGD:5509061 20150430 MGI PMID:24470394 62287 Pten phosphatase and tensin homolog gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:23817021 62287 Pten phosphatase and tensin homolog gene MP:0001270 distended abdomen IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:11178110 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:15619626 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16488991 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16489020 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18381417 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18687666 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:19237610 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:20418913 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22341455 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22836754 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23047698 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20150611 MGI PMID:24986896 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160204 MGI PMID:22331912 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160204 MGI PMID:25815421 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160211 MGI PMID:22350410 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20170105 MGI PMID:26123588 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20170601 MGI PMID:19351816 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20170601 MGI PMID:22190384 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20170601 MGI PMID:24512487 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20170622 MGI PMID:19282848 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20210311 MGI PMID:30401749 62287 Pten phosphatase and tensin homolog gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20220519 MGI PMID:34099734 62287 Pten phosphatase and tensin homolog gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:11691952 62287 Pten phosphatase and tensin homolog gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:20592216 62287 Pten phosphatase and tensin homolog gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200123 MGI PMID:21576358 62287 Pten phosphatase and tensin homolog gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20592216 62287 Pten phosphatase and tensin homolog gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:19208814 62287 Pten phosphatase and tensin homolog gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20150430 MGI PMID:24470394 62287 Pten phosphatase and tensin homolog gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20161117 MGI PMID:25561290 62287 Pten phosphatase and tensin homolog gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18451155 62287 Pten phosphatase and tensin homolog gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18948956 62287 Pten phosphatase and tensin homolog gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19470613 62287 Pten phosphatase and tensin homolog gene MP:0001393 ataxia IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0001396 unidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:18451155 62287 Pten phosphatase and tensin homolog gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20161117 MGI PMID:25561290 62287 Pten phosphatase and tensin homolog gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20210826 MGI PMID:28636948 62287 Pten phosphatase and tensin homolog gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18451155 62287 Pten phosphatase and tensin homolog gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0001525 impaired balance IAGP N RGD:5509061 20150430 MGI PMID:24470394 62287 Pten phosphatase and tensin homolog gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:20348245 62287 Pten phosphatase and tensin homolog gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:23023706 62287 Pten phosphatase and tensin homolog gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18687666 62287 Pten phosphatase and tensin homolog gene MP:0001577 anemia IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18463637 62287 Pten phosphatase and tensin homolog gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:23023706 62287 Pten phosphatase and tensin homolog gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12297047 62287 Pten phosphatase and tensin homolog gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21693517 62287 Pten phosphatase and tensin homolog gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:19185849 62287 Pten phosphatase and tensin homolog gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:19884655 62287 Pten phosphatase and tensin homolog gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:21693517 62287 Pten phosphatase and tensin homolog gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:9799734 62287 Pten phosphatase and tensin homolog gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15492213 62287 Pten phosphatase and tensin homolog gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15755804 62287 Pten phosphatase and tensin homolog gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:15492213 62287 Pten phosphatase and tensin homolog gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:20858757 62287 Pten phosphatase and tensin homolog gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:9799734 62287 Pten phosphatase and tensin homolog gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15755804 62287 Pten phosphatase and tensin homolog gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21266327 62287 Pten phosphatase and tensin homolog gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0001749 suppressed circulating follicle stimulating hormone level IAGP N RGD:5509061 20160811 MGI PMID:26061565 62287 Pten phosphatase and tensin homolog gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:21860425 62287 Pten phosphatase and tensin homolog gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:21860425 62287 Pten phosphatase and tensin homolog gene MP:0001756 abnormal urination IAGP N RGD:5509061 20141003 MGI PMID:16488991 62287 Pten phosphatase and tensin homolog gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20807812 62287 Pten phosphatase and tensin homolog gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:17000121 62287 Pten phosphatase and tensin homolog gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:17567478 62287 Pten phosphatase and tensin homolog gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18281487 62287 Pten phosphatase and tensin homolog gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:19286998 62287 Pten phosphatase and tensin homolog gene MP:0001861 lung inflammation IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10910075 62287 Pten phosphatase and tensin homolog gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11178110 62287 Pten phosphatase and tensin homolog gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12163417 62287 Pten phosphatase and tensin homolog gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16818619 62287 Pten phosphatase and tensin homolog gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19847259 62287 Pten phosphatase and tensin homolog gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20160331 MGI PMID:25330770 62287 Pten phosphatase and tensin homolog gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20231109 MGI PMID:37291517 62287 Pten phosphatase and tensin homolog gene MP:0001885 mammary gland duct hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12163417 62287 Pten phosphatase and tensin homolog gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:19750226 62287 Pten phosphatase and tensin homolog gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23023706 62287 Pten phosphatase and tensin homolog gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:20592216 62287 Pten phosphatase and tensin homolog gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:18601916 62287 Pten phosphatase and tensin homolog gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:20858757 62287 Pten phosphatase and tensin homolog gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18239123 62287 Pten phosphatase and tensin homolog gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19033462 62287 Pten phosphatase and tensin homolog gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:18239123 62287 Pten phosphatase and tensin homolog gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18687666 62287 Pten phosphatase and tensin homolog gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:20858757 62287 Pten phosphatase and tensin homolog gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0001953 respiratory failure IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:20676139 62287 Pten phosphatase and tensin homolog gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:23023706 62287 Pten phosphatase and tensin homolog gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:19211894 62287 Pten phosphatase and tensin homolog gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:22859719 62287 Pten phosphatase and tensin homolog gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20160728 MGI PMID:25377472 62287 Pten phosphatase and tensin homolog gene MP:0002015 epithelioid cyst IAGP N RGD:5509061 20141003 MGI PMID:16204035 62287 Pten phosphatase and tensin homolog gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16169464 62287 Pten phosphatase and tensin homolog gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9697695 62287 Pten phosphatase and tensin homolog gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16818619 62287 Pten phosphatase and tensin homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15492213 62287 Pten phosphatase and tensin homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18043744 62287 Pten phosphatase and tensin homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18474617 62287 Pten phosphatase and tensin homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9799734 62287 Pten phosphatase and tensin homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15492213 62287 Pten phosphatase and tensin homolog gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18043744 62287 Pten phosphatase and tensin homolog gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9799734 62287 Pten phosphatase and tensin homolog gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:16598206 62287 Pten phosphatase and tensin homolog gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:9799734 62287 Pten phosphatase and tensin homolog gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18281487 62287 Pten phosphatase and tensin homolog gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19846776 62287 Pten phosphatase and tensin homolog gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23319880 62287 Pten phosphatase and tensin homolog gene MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10910075 62287 Pten phosphatase and tensin homolog gene MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15492213 62287 Pten phosphatase and tensin homolog gene MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16079851 62287 Pten phosphatase and tensin homolog gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16204035 62287 Pten phosphatase and tensin homolog gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16488991 62287 Pten phosphatase and tensin homolog gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19176372 62287 Pten phosphatase and tensin homolog gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19261747 62287 Pten phosphatase and tensin homolog gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9799734 62287 Pten phosphatase and tensin homolog gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:22331912 62287 Pten phosphatase and tensin homolog gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:25815421 62287 Pten phosphatase and tensin homolog gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20210311 MGI PMID:30401749 62287 Pten phosphatase and tensin homolog gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18281487 62287 Pten phosphatase and tensin homolog gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20170105 MGI PMID:26123588 62287 Pten phosphatase and tensin homolog gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:16204035 62287 Pten phosphatase and tensin homolog gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:21504907 62287 Pten phosphatase and tensin homolog gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:22094257 62287 Pten phosphatase and tensin homolog gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:23873941 62287 Pten phosphatase and tensin homolog gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17607361 62287 Pten phosphatase and tensin homolog gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19185849 62287 Pten phosphatase and tensin homolog gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20679199 62287 Pten phosphatase and tensin homolog gene MP:0002059 abnormal seminal vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18474617 62287 Pten phosphatase and tensin homolog gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:18451155 62287 Pten phosphatase and tensin homolog gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:18948956 62287 Pten phosphatase and tensin homolog gene MP:0002064 seizures IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21266327 62287 Pten phosphatase and tensin homolog gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19289493 62287 Pten phosphatase and tensin homolog gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23047698 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14522255 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15619626 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16079851 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16169464 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16204035 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16488991 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16598206 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16767220 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18281487 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18451155 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18463637 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18632614 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18687666 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19011632 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19168705 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19176372 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19261747 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19470613 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19846776 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20418913 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20592216 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20676139 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20807812 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20818428 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21262837 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21625383 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22214849 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22341455 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22796458 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22836754 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23319880 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23512661 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23817021 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20150611 MGI PMID:24986896 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20151015 MGI PMID:25234167 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20160204 MGI PMID:22331912 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20160204 MGI PMID:25815421 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20160211 MGI PMID:22350410 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20160602 MGI PMID:22863881 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20160728 MGI PMID:25377472 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20160915 MGI PMID:21283818 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20170601 MGI PMID:19351816 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20170601 MGI PMID:22190384 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20170601 MGI PMID:24512487 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20181004 MGI PMID:29720449 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20200806 MGI PMID:31677819 62287 Pten phosphatase and tensin homolog gene MP:0002083 premature death IAGP N RGD:5509061 20220519 MGI PMID:34099734 62287 Pten phosphatase and tensin homolog gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:9799734 62287 Pten phosphatase and tensin homolog gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20160331 MGI PMID:15492213 62287 Pten phosphatase and tensin homolog gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17607361 62287 Pten phosphatase and tensin homolog gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18463637 62287 Pten phosphatase and tensin homolog gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:11691952 62287 Pten phosphatase and tensin homolog gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18474617 62287 Pten phosphatase and tensin homolog gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18281487 62287 Pten phosphatase and tensin homolog gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:11691952 62287 Pten phosphatase and tensin homolog gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:19208814 62287 Pten phosphatase and tensin homolog gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:21343951 62287 Pten phosphatase and tensin homolog gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:23475934 62287 Pten phosphatase and tensin homolog gene MP:0002176 increased brain weight IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:12297047 62287 Pten phosphatase and tensin homolog gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20161020 MGI PMID:26780512 62287 Pten phosphatase and tensin homolog gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:9799734 62287 Pten phosphatase and tensin homolog gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:18493606 62287 Pten phosphatase and tensin homolog gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:18493606 62287 Pten phosphatase and tensin homolog gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0002274 abnormal type I pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:22214849 62287 Pten phosphatase and tensin homolog gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20150709 MGI PMID:20837017 62287 Pten phosphatase and tensin homolog gene MP:0002324 abnormal alveolocapillary membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19168705 62287 Pten phosphatase and tensin homolog gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:19286998 62287 Pten phosphatase and tensin homolog gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:19286998 62287 Pten phosphatase and tensin homolog gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16598206 62287 Pten phosphatase and tensin homolog gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17000121 62287 Pten phosphatase and tensin homolog gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12563260 62287 Pten phosphatase and tensin homolog gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16988010 62287 Pten phosphatase and tensin homolog gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17202315 62287 Pten phosphatase and tensin homolog gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:19286998 62287 Pten phosphatase and tensin homolog gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:17000121 62287 Pten phosphatase and tensin homolog gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:14769918 62287 Pten phosphatase and tensin homolog gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16767220 62287 Pten phosphatase and tensin homolog gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17567478 62287 Pten phosphatase and tensin homolog gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19011632 62287 Pten phosphatase and tensin homolog gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:20348245 62287 Pten phosphatase and tensin homolog gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20150709 MGI PMID:20837017 62287 Pten phosphatase and tensin homolog gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:18474617 62287 Pten phosphatase and tensin homolog gene MP:0002635 reduced sensorimotor gating IAGP N RGD:5509061 20141003 MGI PMID:19208814 62287 Pten phosphatase and tensin homolog gene MP:0002635 reduced sensorimotor gating IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20592216 62287 Pten phosphatase and tensin homolog gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:23319880 62287 Pten phosphatase and tensin homolog gene MP:0002676 uterus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20858757 62287 Pten phosphatase and tensin homolog gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:18239123 62287 Pten phosphatase and tensin homolog gene MP:0002681 increased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:18606860 62287 Pten phosphatase and tensin homolog gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:16537919 62287 Pten phosphatase and tensin homolog gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:14769918 62287 Pten phosphatase and tensin homolog gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14769918 62287 Pten phosphatase and tensin homolog gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15743841 62287 Pten phosphatase and tensin homolog gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19289493 62287 Pten phosphatase and tensin homolog gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20200318 62287 Pten phosphatase and tensin homolog gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21266327 62287 Pten phosphatase and tensin homolog gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:20592216 62287 Pten phosphatase and tensin homolog gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20210826 MGI PMID:31291551 62287 Pten phosphatase and tensin homolog gene MP:0002758 long tail IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0002763 ectopic Bergmann glia cells IAGP N RGD:5509061 20141003 MGI PMID:15944184 62287 Pten phosphatase and tensin homolog gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:18474617 62287 Pten phosphatase and tensin homolog gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20160811 MGI PMID:26061565 62287 Pten phosphatase and tensin homolog gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20170622 MGI PMID:19282848 62287 Pten phosphatase and tensin homolog gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20210826 MGI PMID:28636948 62287 Pten phosphatase and tensin homolog gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:14769918 62287 Pten phosphatase and tensin homolog gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15743841 62287 Pten phosphatase and tensin homolog gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20852026 62287 Pten phosphatase and tensin homolog gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22302806 62287 Pten phosphatase and tensin homolog gene MP:0002915 abnormal synaptic depression IAGP N RGD:5509061 20161020 MGI PMID:26780512 62287 Pten phosphatase and tensin homolog gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16767220 62287 Pten phosphatase and tensin homolog gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17567478 62287 Pten phosphatase and tensin homolog gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20150709 MGI PMID:20837017 62287 Pten phosphatase and tensin homolog gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:16818619 62287 Pten phosphatase and tensin homolog gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19011632 62287 Pten phosphatase and tensin homolog gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:17567478 62287 Pten phosphatase and tensin homolog gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20170119 MGI PMID:27573812 62287 Pten phosphatase and tensin homolog gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:14769918 62287 Pten phosphatase and tensin homolog gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16767220 62287 Pten phosphatase and tensin homolog gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19011632 62287 Pten phosphatase and tensin homolog gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20348245 62287 Pten phosphatase and tensin homolog gene MP:0002981 increased liver weight IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0002981 increased liver weight IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20210826 MGI PMID:29969932 62287 Pten phosphatase and tensin homolog gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:19038262 62287 Pten phosphatase and tensin homolog gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20852026 62287 Pten phosphatase and tensin homolog gene MP:0003075 abnormal response to CNS ischemic injury IAGP N RGD:5509061 20141003 MGI PMID:19211894 62287 Pten phosphatase and tensin homolog gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:20858757 62287 Pten phosphatase and tensin homolog gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19750226 62287 Pten phosphatase and tensin homolog gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:9799734 62287 Pten phosphatase and tensin homolog gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:19168705 62287 Pten phosphatase and tensin homolog gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:19011632 62287 Pten phosphatase and tensin homolog gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17567478 62287 Pten phosphatase and tensin homolog gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16767220 62287 Pten phosphatase and tensin homolog gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17567478 62287 Pten phosphatase and tensin homolog gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19011632 62287 Pten phosphatase and tensin homolog gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20150709 MGI PMID:20837017 62287 Pten phosphatase and tensin homolog gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17567478 62287 Pten phosphatase and tensin homolog gene MP:0003354 astrocytosis IAGP N RGD:5509061 20150430 MGI PMID:24470394 62287 Pten phosphatase and tensin homolog gene MP:0003357 impaired granulosa cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21860425 62287 Pten phosphatase and tensin homolog gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:15492213 62287 Pten phosphatase and tensin homolog gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22341455 62287 Pten phosphatase and tensin homolog gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:19847259 62287 Pten phosphatase and tensin homolog gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19168705 62287 Pten phosphatase and tensin homolog gene MP:0003462 abnormal response to novel odor IAGP N RGD:5509061 20141003 MGI PMID:19211894 62287 Pten phosphatase and tensin homolog gene MP:0003496 increased thyroid adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20676139 62287 Pten phosphatase and tensin homolog gene MP:0003496 increased thyroid adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0003496 increased thyroid adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22167068 62287 Pten phosphatase and tensin homolog gene MP:0003498 thyroid gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20676139 62287 Pten phosphatase and tensin homolog gene MP:0003498 thyroid gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22167068 62287 Pten phosphatase and tensin homolog gene MP:0003502 increased activity of thyroid gland IAGP N RGD:5509061 20170601 MGI PMID:24512487 62287 Pten phosphatase and tensin homolog gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20141003 MGI PMID:18601916 62287 Pten phosphatase and tensin homolog gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20141003 MGI PMID:22214849 62287 Pten phosphatase and tensin homolog gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20141003 MGI PMID:18474617 62287 Pten phosphatase and tensin homolog gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20160204 MGI PMID:22331912 62287 Pten phosphatase and tensin homolog gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:22331912 62287 Pten phosphatase and tensin homolog gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:25815421 62287 Pten phosphatase and tensin homolog gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20160714 MGI PMID:17418409 62287 Pten phosphatase and tensin homolog gene MP:0003597 increased epididymal cystadenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18474617 62287 Pten phosphatase and tensin homolog gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:16079851 62287 Pten phosphatase and tensin homolog gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:14522255 62287 Pten phosphatase and tensin homolog gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:23817021 62287 Pten phosphatase and tensin homolog gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20220303 MGI PMID:16288012 62287 Pten phosphatase and tensin homolog gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20220303 MGI PMID:17607361 62287 Pten phosphatase and tensin homolog gene MP:0003608 prostate gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:14522255 62287 Pten phosphatase and tensin homolog gene MP:0003630 abnormal urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16951148 62287 Pten phosphatase and tensin homolog gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:23319880 62287 Pten phosphatase and tensin homolog gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:19750226 62287 Pten phosphatase and tensin homolog gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:22302806 62287 Pten phosphatase and tensin homolog gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:16537919 62287 Pten phosphatase and tensin homolog gene MP:0003674 oxidative stress IAGP N RGD:5509061 20150709 MGI PMID:20837017 62287 Pten phosphatase and tensin homolog gene MP:0003674 oxidative stress IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18497742 62287 Pten phosphatase and tensin homolog gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20150430 MGI PMID:24470394 62287 Pten phosphatase and tensin homolog gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:22341455 62287 Pten phosphatase and tensin homolog gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21625383 62287 Pten phosphatase and tensin homolog gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0003752 increased oral papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:22859719 62287 Pten phosphatase and tensin homolog gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:21952241 62287 Pten phosphatase and tensin homolog gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:19286998 62287 Pten phosphatase and tensin homolog gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20161117 MGI PMID:25561290 62287 Pten phosphatase and tensin homolog gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:20592216 62287 Pten phosphatase and tensin homolog gene MP:0003875 abnormal hair follicle regression IAGP N RGD:5509061 20141003 MGI PMID:16204035 62287 Pten phosphatase and tensin homolog gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20150709 MGI PMID:20837017 62287 Pten phosphatase and tensin homolog gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17567478 62287 Pten phosphatase and tensin homolog gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20150709 MGI PMID:20837017 62287 Pten phosphatase and tensin homolog gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:18497742 62287 Pten phosphatase and tensin homolog gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12297047 62287 Pten phosphatase and tensin homolog gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9799734 62287 Pten phosphatase and tensin homolog gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:9799734 62287 Pten phosphatase and tensin homolog gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19470613 62287 Pten phosphatase and tensin homolog gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20141003 MGI PMID:19168705 62287 Pten phosphatase and tensin homolog gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23023706 62287 Pten phosphatase and tensin homolog gene MP:0004049 increased acute promyelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:16598206 62287 Pten phosphatase and tensin homolog gene MP:0004049 increased acute promyelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:18463637 62287 Pten phosphatase and tensin homolog gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:19750226 62287 Pten phosphatase and tensin homolog gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20200318 62287 Pten phosphatase and tensin homolog gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15944184 62287 Pten phosphatase and tensin homolog gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15492213 62287 Pten phosphatase and tensin homolog gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:15755804 62287 Pten phosphatase and tensin homolog gene MP:0004202 pulmonary hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0004202 pulmonary hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19574443 62287 Pten phosphatase and tensin homolog gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16488991 62287 Pten phosphatase and tensin homolog gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22859719 62287 Pten phosphatase and tensin homolog gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24124460 62287 Pten phosphatase and tensin homolog gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20858757 62287 Pten phosphatase and tensin homolog gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:19211894 62287 Pten phosphatase and tensin homolog gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20823247 62287 Pten phosphatase and tensin homolog gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16951148 62287 Pten phosphatase and tensin homolog gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:18043744 62287 Pten phosphatase and tensin homolog gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:9799734 62287 Pten phosphatase and tensin homolog gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:15492213 62287 Pten phosphatase and tensin homolog gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:12297047 62287 Pten phosphatase and tensin homolog gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:22167068 62287 Pten phosphatase and tensin homolog gene MP:0004697 abnormal thyroid follicular cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0004697 abnormal thyroid follicular cell morphology IAGP N RGD:5509061 20170601 MGI PMID:24512487 62287 Pten phosphatase and tensin homolog gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22302806 62287 Pten phosphatase and tensin homolog gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:17540362 62287 Pten phosphatase and tensin homolog gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:17000121 62287 Pten phosphatase and tensin homolog gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:18178811 62287 Pten phosphatase and tensin homolog gene MP:0004832 enlarged ovary IAGP N RGD:5509061 20141003 MGI PMID:18239123 62287 Pten phosphatase and tensin homolog gene MP:0004832 enlarged ovary IAGP N RGD:5509061 20141003 MGI PMID:18601916 62287 Pten phosphatase and tensin homolog gene MP:0004832 enlarged ovary IAGP N RGD:5509061 20141003 MGI PMID:18606860 62287 Pten phosphatase and tensin homolog gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22214849 62287 Pten phosphatase and tensin homolog gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16767220 62287 Pten phosphatase and tensin homolog gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:19168705 62287 Pten phosphatase and tensin homolog gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19168705 62287 Pten phosphatase and tensin homolog gene MP:0004848 abnormal liver size IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10910075 62287 Pten phosphatase and tensin homolog gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15492213 62287 Pten phosphatase and tensin homolog gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15619626 62287 Pten phosphatase and tensin homolog gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18632614 62287 Pten phosphatase and tensin homolog gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20418913 62287 Pten phosphatase and tensin homolog gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20160728 MGI PMID:25377472 62287 Pten phosphatase and tensin homolog gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:18474617 62287 Pten phosphatase and tensin homolog gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:20418913 62287 Pten phosphatase and tensin homolog gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:20858757 62287 Pten phosphatase and tensin homolog gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:20418913 62287 Pten phosphatase and tensin homolog gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20160728 MGI PMID:25377472 62287 Pten phosphatase and tensin homolog gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20160728 MGI PMID:25377472 62287 Pten phosphatase and tensin homolog gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:18632614 62287 Pten phosphatase and tensin homolog gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:19011632 62287 Pten phosphatase and tensin homolog gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20161117 MGI PMID:25561290 62287 Pten phosphatase and tensin homolog gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18474617 62287 Pten phosphatase and tensin homolog gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17540362 62287 Pten phosphatase and tensin homolog gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0004944 abnormal B cell negative selection IAGP N RGD:5509061 20141003 MGI PMID:19896393 62287 Pten phosphatase and tensin homolog gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:19211894 62287 Pten phosphatase and tensin homolog gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15958561 62287 Pten phosphatase and tensin homolog gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16818619 62287 Pten phosphatase and tensin homolog gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0004958 enlarged prostate gland IAGP N RGD:5509061 20141003 MGI PMID:14522255 62287 Pten phosphatase and tensin homolog gene MP:0004958 enlarged prostate gland IAGP N RGD:5509061 20141003 MGI PMID:14691534 62287 Pten phosphatase and tensin homolog gene MP:0004958 enlarged prostate gland IAGP N RGD:5509061 20141003 MGI PMID:16489020 62287 Pten phosphatase and tensin homolog gene MP:0004958 enlarged prostate gland IAGP N RGD:5509061 20141003 MGI PMID:23817021 62287 Pten phosphatase and tensin homolog gene MP:0004961 increased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:15994948 62287 Pten phosphatase and tensin homolog gene MP:0004961 increased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:17607361 62287 Pten phosphatase and tensin homolog gene MP:0004961 increased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0004962 decreased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:17607361 62287 Pten phosphatase and tensin homolog gene MP:0004967 abnormal kidney epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18497742 62287 Pten phosphatase and tensin homolog gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563260 62287 Pten phosphatase and tensin homolog gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:11691952 62287 Pten phosphatase and tensin homolog gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:19211894 62287 Pten phosphatase and tensin homolog gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563260 62287 Pten phosphatase and tensin homolog gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20858757 62287 Pten phosphatase and tensin homolog gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0005084 abnormal gallbladder morphology IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0005119 decreased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20170601 MGI PMID:19351816 62287 Pten phosphatase and tensin homolog gene MP:0005131 increased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:18239123 62287 Pten phosphatase and tensin homolog gene MP:0005133 increased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:18239123 62287 Pten phosphatase and tensin homolog gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:20676139 62287 Pten phosphatase and tensin homolog gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20170601 MGI PMID:22190384 62287 Pten phosphatase and tensin homolog gene MP:0005135 increased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:22167068 62287 Pten phosphatase and tensin homolog gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12297047 62287 Pten phosphatase and tensin homolog gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12563260 62287 Pten phosphatase and tensin homolog gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19896393 62287 Pten phosphatase and tensin homolog gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:20694004 62287 Pten phosphatase and tensin homolog gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:16537919 62287 Pten phosphatase and tensin homolog gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:19574443 62287 Pten phosphatase and tensin homolog gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:21860425 62287 Pten phosphatase and tensin homolog gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:21860425 62287 Pten phosphatase and tensin homolog gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0005202 lethargy IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:20852026 62287 Pten phosphatase and tensin homolog gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20852026 62287 Pten phosphatase and tensin homolog gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21266327 62287 Pten phosphatase and tensin homolog gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:16169464 62287 Pten phosphatase and tensin homolog gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:20807812 62287 Pten phosphatase and tensin homolog gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:11691952 62287 Pten phosphatase and tensin homolog gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:15944184 62287 Pten phosphatase and tensin homolog gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:19151711 62287 Pten phosphatase and tensin homolog gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:19470613 62287 Pten phosphatase and tensin homolog gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:20592216 62287 Pten phosphatase and tensin homolog gene MP:0005238 increased brain size IAGP N RGD:5509061 20150430 MGI PMID:24470394 62287 Pten phosphatase and tensin homolog gene MP:0005238 increased brain size IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:11691952 62287 Pten phosphatase and tensin homolog gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:14769918 62287 Pten phosphatase and tensin homolog gene MP:0005284 increased saturated fatty acids level IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:14769918 62287 Pten phosphatase and tensin homolog gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15743841 62287 Pten phosphatase and tensin homolog gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20852026 62287 Pten phosphatase and tensin homolog gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19289493 62287 Pten phosphatase and tensin homolog gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20348245 62287 Pten phosphatase and tensin homolog gene MP:0005305 prostate gland anterior lobe hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:14691534 62287 Pten phosphatase and tensin homolog gene MP:0005305 prostate gland anterior lobe hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:16488991 62287 Pten phosphatase and tensin homolog gene MP:0005324 ascites IAGP N RGD:5509061 20160204 MGI PMID:22331912 62287 Pten phosphatase and tensin homolog gene MP:0005324 ascites IAGP N RGD:5509061 20160204 MGI PMID:25815421 62287 Pten phosphatase and tensin homolog gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17540362 62287 Pten phosphatase and tensin homolog gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:20852026 62287 Pten phosphatase and tensin homolog gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:21952241 62287 Pten phosphatase and tensin homolog gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:22167068 62287 Pten phosphatase and tensin homolog gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20170601 MGI PMID:19351816 62287 Pten phosphatase and tensin homolog gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20170601 MGI PMID:22190384 62287 Pten phosphatase and tensin homolog gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20170601 MGI PMID:24512487 62287 Pten phosphatase and tensin homolog gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20160811 MGI PMID:26061565 62287 Pten phosphatase and tensin homolog gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0005426 tachypnea IAGP N RGD:5509061 20141003 MGI PMID:18281487 62287 Pten phosphatase and tensin homolog gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:20676139 62287 Pten phosphatase and tensin homolog gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:22167068 62287 Pten phosphatase and tensin homolog gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20170601 MGI PMID:19351816 62287 Pten phosphatase and tensin homolog gene MP:0005471 decreased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:22167068 62287 Pten phosphatase and tensin homolog gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:21952241 62287 Pten phosphatase and tensin homolog gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20170601 MGI PMID:24512487 62287 Pten phosphatase and tensin homolog gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:21952241 62287 Pten phosphatase and tensin homolog gene MP:0005488 bronchial epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17921358 62287 Pten phosphatase and tensin homolog gene MP:0005488 bronchial epithelial hyperplasia IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0005490 increased club cell number IAGP N RGD:5509061 20141003 MGI PMID:17921358 62287 Pten phosphatase and tensin homolog gene MP:0005490 increased club cell number IAGP N RGD:5509061 20141003 MGI PMID:19574443 62287 Pten phosphatase and tensin homolog gene MP:0005490 increased club cell number IAGP N RGD:5509061 20141003 MGI PMID:20147383 62287 Pten phosphatase and tensin homolog gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16169464 62287 Pten phosphatase and tensin homolog gene MP:0005502 abnormal renal/urinary system physiology IAGP N RGD:5509061 20141003 MGI PMID:17607361 62287 Pten phosphatase and tensin homolog gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:20554973 62287 Pten phosphatase and tensin homolog gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:14769918 62287 Pten phosphatase and tensin homolog gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20200318 62287 Pten phosphatase and tensin homolog gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12297047 62287 Pten phosphatase and tensin homolog gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15958561 62287 Pten phosphatase and tensin homolog gene MP:0005603 neuron hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19470613 62287 Pten phosphatase and tensin homolog gene MP:0005603 neuron hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19750226 62287 Pten phosphatase and tensin homolog gene MP:0005603 neuron hypertrophy IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:20554973 62287 Pten phosphatase and tensin homolog gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23475934 62287 Pten phosphatase and tensin homolog gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:14769918 62287 Pten phosphatase and tensin homolog gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20210826 MGI PMID:29969932 62287 Pten phosphatase and tensin homolog gene MP:0006078 abnormal nipple morphology IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19237610 62287 Pten phosphatase and tensin homolog gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21860425 62287 Pten phosphatase and tensin homolog gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:12163417 62287 Pten phosphatase and tensin homolog gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:12163417 62287 Pten phosphatase and tensin homolog gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:20554973 62287 Pten phosphatase and tensin homolog gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17921358 62287 Pten phosphatase and tensin homolog gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:18327259 62287 Pten phosphatase and tensin homolog gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:18832389 62287 Pten phosphatase and tensin homolog gene MP:0006422 increased mammary adenoacanthoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18687666 62287 Pten phosphatase and tensin homolog gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20505730 62287 Pten phosphatase and tensin homolog gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21860425 62287 Pten phosphatase and tensin homolog gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22214849 62287 Pten phosphatase and tensin homolog gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:17237784 62287 Pten phosphatase and tensin homolog gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:18043744 62287 Pten phosphatase and tensin homolog gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:19168705 62287 Pten phosphatase and tensin homolog gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18281487 62287 Pten phosphatase and tensin homolog gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20160602 MGI PMID:22863881 62287 Pten phosphatase and tensin homolog gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20150709 MGI PMID:20837017 62287 Pten phosphatase and tensin homolog gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:20592216 62287 Pten phosphatase and tensin homolog gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:14769918 62287 Pten phosphatase and tensin homolog gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20200123 MGI PMID:21576358 62287 Pten phosphatase and tensin homolog gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:19168705 62287 Pten phosphatase and tensin homolog gene MP:0008136 enlarged Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:10910075 62287 Pten phosphatase and tensin homolog gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19151711 62287 Pten phosphatase and tensin homolog gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22302806 62287 Pten phosphatase and tensin homolog gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:18327259 62287 Pten phosphatase and tensin homolog gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:20826752 62287 Pten phosphatase and tensin homolog gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563260 62287 Pten phosphatase and tensin homolog gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18178811 62287 Pten phosphatase and tensin homolog gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:19286998 62287 Pten phosphatase and tensin homolog gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:20858757 62287 Pten phosphatase and tensin homolog gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0008413 decreased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:16537919 62287 Pten phosphatase and tensin homolog gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:11691952 62287 Pten phosphatase and tensin homolog gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:12563260 62287 Pten phosphatase and tensin homolog gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19884655 62287 Pten phosphatase and tensin homolog gene MP:0008490 enlarged dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:23319880 62287 Pten phosphatase and tensin homolog gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20826752 62287 Pten phosphatase and tensin homolog gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20200123 MGI PMID:21576358 62287 Pten phosphatase and tensin homolog gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:21576358 62287 Pten phosphatase and tensin homolog gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:21576358 62287 Pten phosphatase and tensin homolog gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200123 MGI PMID:21576358 62287 Pten phosphatase and tensin homolog gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20150430 MGI PMID:24470394 62287 Pten phosphatase and tensin homolog gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20210826 MGI PMID:31291551 62287 Pten phosphatase and tensin homolog gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:20823247 62287 Pten phosphatase and tensin homolog gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:15743841 62287 Pten phosphatase and tensin homolog gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:19286998 62287 Pten phosphatase and tensin homolog gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18281487 62287 Pten phosphatase and tensin homolog gene MP:0008715 increased lung small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23047698 62287 Pten phosphatase and tensin homolog gene MP:0008717 increased lung squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:19286998 62287 Pten phosphatase and tensin homolog gene MP:0008728 increased memory B cell number IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0008746 abnormal peripheral B cell anergy IAGP N RGD:5509061 20141003 MGI PMID:19896393 62287 Pten phosphatase and tensin homolog gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20170601 MGI PMID:24512487 62287 Pten phosphatase and tensin homolog gene MP:0008780 increased pancreatic acinar cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16169464 62287 Pten phosphatase and tensin homolog gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12563260 62287 Pten phosphatase and tensin homolog gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:19470613 62287 Pten phosphatase and tensin homolog gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20170601 MGI PMID:24512487 62287 Pten phosphatase and tensin homolog gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20170601 MGI PMID:24512487 62287 Pten phosphatase and tensin homolog gene MP:0008876 decreased uterine NK cell number IAGP N RGD:5509061 20141003 MGI PMID:20858757 62287 Pten phosphatase and tensin homolog gene MP:0008914 enlarged cerebellum IAGP N RGD:5509061 20141003 MGI PMID:12091320 62287 Pten phosphatase and tensin homolog gene MP:0008914 enlarged cerebellum IAGP N RGD:5509061 20141003 MGI PMID:15944184 62287 Pten phosphatase and tensin homolog gene MP:0008914 enlarged cerebellum IAGP N RGD:5509061 20150430 MGI PMID:24470394 62287 Pten phosphatase and tensin homolog gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21896734 62287 Pten phosphatase and tensin homolog gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0009053 abnormal anal canal morphology IAGP N RGD:5509061 20141003 MGI PMID:24124460 62287 Pten phosphatase and tensin homolog gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10910075 62287 Pten phosphatase and tensin homolog gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18043744 62287 Pten phosphatase and tensin homolog gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18474617 62287 Pten phosphatase and tensin homolog gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18632614 62287 Pten phosphatase and tensin homolog gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19011632 62287 Pten phosphatase and tensin homolog gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20418913 62287 Pten phosphatase and tensin homolog gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20858757 62287 Pten phosphatase and tensin homolog gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20160728 MGI PMID:25377472 62287 Pten phosphatase and tensin homolog gene MP:0009105 penis prolapse IAGP N RGD:5509061 20141003 MGI PMID:23817021 62287 Pten phosphatase and tensin homolog gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:20852026 62287 Pten phosphatase and tensin homolog gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:21266327 62287 Pten phosphatase and tensin homolog gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:21266327 62287 Pten phosphatase and tensin homolog gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:19208814 62287 Pten phosphatase and tensin homolog gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:16169464 62287 Pten phosphatase and tensin homolog gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16169464 62287 Pten phosphatase and tensin homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16169464 62287 Pten phosphatase and tensin homolog gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20807812 62287 Pten phosphatase and tensin homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:16169464 62287 Pten phosphatase and tensin homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:20807812 62287 Pten phosphatase and tensin homolog gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20807812 62287 Pten phosphatase and tensin homolog gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20160602 MGI PMID:22863881 62287 Pten phosphatase and tensin homolog gene MP:0009159 increased pancreatic acinar cell number IAGP N RGD:5509061 20141003 MGI PMID:16169464 62287 Pten phosphatase and tensin homolog gene MP:0009164 exocrine pancreas atrophy IAGP N RGD:5509061 20141120 MGI PMID:20807812 62287 Pten phosphatase and tensin homolog gene MP:0009167 increased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:16537919 62287 Pten phosphatase and tensin homolog gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:16169464 62287 Pten phosphatase and tensin homolog gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:16537919 62287 Pten phosphatase and tensin homolog gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19289493 62287 Pten phosphatase and tensin homolog gene MP:0009216 abnormal peritoneum morphology IAGP N RGD:5509061 20141003 MGI PMID:22214849 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:11854455 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:14522255 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:15994948 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:16079851 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:16288012 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:16489020 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:18043744 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:18245377 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:18594509 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:19033462 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:19081794 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:19185849 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:19741607 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:20679199 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:21572435 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22341455 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22505453 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22836754 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:23150596 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:23512661 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:23817021 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20150611 MGI PMID:24986896 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20170323 MGI PMID:27345403 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20181004 MGI PMID:29720449 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20190207 MGI PMID:28292441 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20191212 MGI PMID:27020859 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20210311 MGI PMID:30401749 62287 Pten phosphatase and tensin homolog gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20220519 MGI PMID:34099734 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14522255 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15994948 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16079851 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16288012 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16489020 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17607361 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19033462 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19081794 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19185849 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19741607 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20679199 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21572435 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21620777 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22341455 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22505453 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22836754 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23512661 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23817021 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20150611 MGI PMID:24986896 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20160211 MGI PMID:22350410 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20170323 MGI PMID:27345403 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20181004 MGI PMID:29720449 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20190207 MGI PMID:28292441 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20191212 MGI PMID:27020859 62287 Pten phosphatase and tensin homolog gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20210311 MGI PMID:30401749 62287 Pten phosphatase and tensin homolog gene MP:0009223 increased uterus carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18451155 62287 Pten phosphatase and tensin homolog gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11178110 62287 Pten phosphatase and tensin homolog gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22214849 62287 Pten phosphatase and tensin homolog gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16488991 62287 Pten phosphatase and tensin homolog gene MP:0009317 increased follicular lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0009318 increased splenic marginal zone lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0009343 dilated gallbladder IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17567478 62287 Pten phosphatase and tensin homolog gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20348245 62287 Pten phosphatase and tensin homolog gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20150611 MGI PMID:14769918 62287 Pten phosphatase and tensin homolog gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0009361 abnormal primordial ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18239123 62287 Pten phosphatase and tensin homolog gene MP:0009361 abnormal primordial ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18601916 62287 Pten phosphatase and tensin homolog gene MP:0009361 abnormal primordial ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19587782 62287 Pten phosphatase and tensin homolog gene MP:0009361 abnormal primordial ovarian follicle morphology IAGP N RGD:5509061 20220407 MGI PMID:19843540 62287 Pten phosphatase and tensin homolog gene MP:0009469 increased skin hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23873941 62287 Pten phosphatase and tensin homolog gene MP:0009480 distended cecum IAGP N RGD:5509061 20141003 MGI PMID:19884655 62287 Pten phosphatase and tensin homolog gene MP:0009493 abnormal cystic duct morphology IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0009498 abnormal extrahepatic bile duct morphology IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12163417 62287 Pten phosphatase and tensin homolog gene MP:0009505 abnormal mammary gland lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:12163417 62287 Pten phosphatase and tensin homolog gene MP:0009508 increased mammary gland ductal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11178110 62287 Pten phosphatase and tensin homolog gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16488991 62287 Pten phosphatase and tensin homolog gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19261747 62287 Pten phosphatase and tensin homolog gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20818428 62287 Pten phosphatase and tensin homolog gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20160915 MGI PMID:21283818 62287 Pten phosphatase and tensin homolog gene MP:0009551 increased urinary bladder transitional cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16951148 62287 Pten phosphatase and tensin homolog gene MP:0009552 urinary bladder obstruction IAGP N RGD:5509061 20141003 MGI PMID:16079851 62287 Pten phosphatase and tensin homolog gene MP:0009552 urinary bladder obstruction IAGP N RGD:5509061 20141003 MGI PMID:22505453 62287 Pten phosphatase and tensin homolog gene MP:0009552 urinary bladder obstruction IAGP N RGD:5509061 20160915 MGI PMID:21283818 62287 Pten phosphatase and tensin homolog gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16204035 62287 Pten phosphatase and tensin homolog gene MP:0009586 increased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:20554973 62287 Pten phosphatase and tensin homolog gene MP:0009612 thick epidermis suprabasal layer IAGP N RGD:5509061 20141003 MGI PMID:23873941 62287 Pten phosphatase and tensin homolog gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:15492213 62287 Pten phosphatase and tensin homolog gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:9799734 62287 Pten phosphatase and tensin homolog gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:18687666 62287 Pten phosphatase and tensin homolog gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20160728 MGI PMID:20418913 62287 Pten phosphatase and tensin homolog gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20160728 MGI PMID:25377472 62287 Pten phosphatase and tensin homolog gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18043744 62287 Pten phosphatase and tensin homolog gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22094257 62287 Pten phosphatase and tensin homolog gene MP:0009715 thick epidermis stratum basale IAGP N RGD:5509061 20141003 MGI PMID:23873941 62287 Pten phosphatase and tensin homolog gene MP:0009734 abnormal prostate gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:19185849 62287 Pten phosphatase and tensin homolog gene MP:0009737 prostate gland cyst IAGP N RGD:5509061 20141003 MGI PMID:23512661 62287 Pten phosphatase and tensin homolog gene MP:0009738 enlarged prostate gland anterior lobe IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19750226 62287 Pten phosphatase and tensin homolog gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210826 MGI PMID:29969932 62287 Pten phosphatase and tensin homolog gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19286998 62287 Pten phosphatase and tensin homolog gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19286998 62287 Pten phosphatase and tensin homolog gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20150709 MGI PMID:20837017 62287 Pten phosphatase and tensin homolog gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19211894 62287 Pten phosphatase and tensin homolog gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20150430 MGI PMID:24470394 62287 Pten phosphatase and tensin homolog gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20150430 MGI PMID:24470394 62287 Pten phosphatase and tensin homolog gene MP:0009951 abnormal olfactory bulb mitral cell layer morphology IAGP N RGD:5509061 20210826 MGI PMID:31291551 62287 Pten phosphatase and tensin homolog gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20150430 MGI PMID:24470394 62287 Pten phosphatase and tensin homolog gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:14769918 62287 Pten phosphatase and tensin homolog gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17567478 62287 Pten phosphatase and tensin homolog gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141003 MGI PMID:20592216 62287 Pten phosphatase and tensin homolog gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20161201 MGI PMID:25621497 62287 Pten phosphatase and tensin homolog gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19168705 62287 Pten phosphatase and tensin homolog gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20150430 MGI PMID:24470394 62287 Pten phosphatase and tensin homolog gene MP:0010171 abnormal centroacinar cell of Langerhans morphology IAGP N RGD:5509061 20141003 MGI PMID:16169464 62287 Pten phosphatase and tensin homolog gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:20826752 62287 Pten phosphatase and tensin homolog gene MP:0010204 abnormal astrocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15958561 62287 Pten phosphatase and tensin homolog gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19847259 62287 Pten phosphatase and tensin homolog gene MP:0010273 increased classified tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19846776 62287 Pten phosphatase and tensin homolog gene MP:0010274 increased organ/body region tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24124460 62287 Pten phosphatase and tensin homolog gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20048081 62287 Pten phosphatase and tensin homolog gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20160114 MGI PMID:25705882 62287 Pten phosphatase and tensin homolog gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15958561 62287 Pten phosphatase and tensin homolog gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18451155 62287 Pten phosphatase and tensin homolog gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18948956 62287 Pten phosphatase and tensin homolog gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23887970 62287 Pten phosphatase and tensin homolog gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20160922 MGI PMID:26704996 62287 Pten phosphatase and tensin homolog gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:18948956 62287 Pten phosphatase and tensin homolog gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20141003 MGI PMID:23887970 62287 Pten phosphatase and tensin homolog gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20160922 MGI PMID:26704996 62287 Pten phosphatase and tensin homolog gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20170314 MGI PMID:27815386 62287 Pten phosphatase and tensin homolog gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18043744 62287 Pten phosphatase and tensin homolog gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0010281 increased nervous system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23887970 62287 Pten phosphatase and tensin homolog gene MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20151015 MGI PMID:25234167 62287 Pten phosphatase and tensin homolog gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10910075 62287 Pten phosphatase and tensin homolog gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12163417 62287 Pten phosphatase and tensin homolog gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18381417 62287 Pten phosphatase and tensin homolog gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19847259 62287 Pten phosphatase and tensin homolog gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20160331 MGI PMID:25330770 62287 Pten phosphatase and tensin homolog gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16204035 62287 Pten phosphatase and tensin homolog gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16204035 62287 Pten phosphatase and tensin homolog gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10910075 62287 Pten phosphatase and tensin homolog gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11726926 62287 Pten phosphatase and tensin homolog gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:16204035 62287 Pten phosphatase and tensin homolog gene MP:0010312 increased oligodendroglioma incidence IAGP N RGD:5509061 20141003 MGI PMID:23887970 62287 Pten phosphatase and tensin homolog gene MP:0010312 increased oligodendroglioma incidence IAGP N RGD:5509061 20160922 MGI PMID:26704996 62287 Pten phosphatase and tensin homolog gene MP:0010314 increased neurofibroma incidence IAGP N RGD:5509061 20141003 MGI PMID:19846776 62287 Pten phosphatase and tensin homolog gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16767220 62287 Pten phosphatase and tensin homolog gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20150709 MGI PMID:20837017 62287 Pten phosphatase and tensin homolog gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22167068 62287 Pten phosphatase and tensin homolog gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23047698 62287 Pten phosphatase and tensin homolog gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20160811 MGI PMID:26359368 62287 Pten phosphatase and tensin homolog gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22796458 62287 Pten phosphatase and tensin homolog gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20170622 MGI PMID:19282848 62287 Pten phosphatase and tensin homolog gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:16598206 62287 Pten phosphatase and tensin homolog gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:18463637 62287 Pten phosphatase and tensin homolog gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21262837 62287 Pten phosphatase and tensin homolog gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20151015 MGI PMID:25234167 62287 Pten phosphatase and tensin homolog gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20676139 62287 Pten phosphatase and tensin homolog gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21952241 62287 Pten phosphatase and tensin homolog gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20170601 MGI PMID:19351816 62287 Pten phosphatase and tensin homolog gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20170601 MGI PMID:22190384 62287 Pten phosphatase and tensin homolog gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20170601 MGI PMID:24512487 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10910075 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11854455 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14691534 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15994948 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16079851 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16288012 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16488991 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16818619 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17607361 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18043744 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19033462 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21620777 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22836754 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23150596 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20150611 MGI PMID:24986896 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20210311 MGI PMID:30401749 62287 Pten phosphatase and tensin homolog gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20220519 MGI PMID:34099734 62287 Pten phosphatase and tensin homolog gene MP:0010364 increased fibroadenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10910075 62287 Pten phosphatase and tensin homolog gene MP:0010364 increased fibroadenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12163417 62287 Pten phosphatase and tensin homolog gene MP:0010367 increased spindle cell carcinoma incidence IAGP N RGD:5509061 20160331 MGI PMID:25330770 62287 Pten phosphatase and tensin homolog gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18474617 62287 Pten phosphatase and tensin homolog gene MP:0010384 increased renal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16488991 62287 Pten phosphatase and tensin homolog gene MP:0010387 abnormal Bergmann glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15944184 62287 Pten phosphatase and tensin homolog gene MP:0010388 abnormal Bergmann glial cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15944184 62287 Pten phosphatase and tensin homolog gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:14769918 62287 Pten phosphatase and tensin homolog gene MP:0010688 hair follicle outer root sheath hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16204035 62287 Pten phosphatase and tensin homolog gene MP:0010690 thick hair follicle outer root sheath IAGP N RGD:5509061 20141003 MGI PMID:16204035 62287 Pten phosphatase and tensin homolog gene MP:0010727 increased glioblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18948956 62287 Pten phosphatase and tensin homolog gene MP:0010727 increased glioblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19196966 62287 Pten phosphatase and tensin homolog gene MP:0010727 increased glioblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21625383 62287 Pten phosphatase and tensin homolog gene MP:0010727 increased glioblastoma incidence IAGP N RGD:5509061 20200806 MGI PMID:31677819 62287 Pten phosphatase and tensin homolog gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:19286998 62287 Pten phosphatase and tensin homolog gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16598206 62287 Pten phosphatase and tensin homolog gene MP:0010799 stomach mucosa hyperplasia IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0010802 abnormal intestinal enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19168705 62287 Pten phosphatase and tensin homolog gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0010827 small lung saccule IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0010829 increased bronchioalveolar stem cell number IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0010890 decreased alveolar lamellar body number IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0010910 bronchiolar epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0010910 bronchiolar epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17921358 62287 Pten phosphatase and tensin homolog gene MP:0010915 increased solitary pulmonary neuroendocrine cell number IAGP N RGD:5509061 20141003 MGI PMID:17921358 62287 Pten phosphatase and tensin homolog gene MP:0010918 abnormal pulmonary neuroendocrine body morphology IAGP N RGD:5509061 20141003 MGI PMID:23047698 62287 Pten phosphatase and tensin homolog gene MP:0010942 abnormal respiratory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17921358 62287 Pten phosphatase and tensin homolog gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20210826 MGI PMID:29969932 62287 Pten phosphatase and tensin homolog gene MP:0010980 ectopic ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:17540362 62287 Pten phosphatase and tensin homolog gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:18497742 62287 Pten phosphatase and tensin homolog gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15944184 62287 Pten phosphatase and tensin homolog gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17540362 62287 Pten phosphatase and tensin homolog gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19884655 62287 Pten phosphatase and tensin homolog gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20807812 62287 Pten phosphatase and tensin homolog gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22167068 62287 Pten phosphatase and tensin homolog gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18757421 62287 Pten phosphatase and tensin homolog gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11691952 62287 Pten phosphatase and tensin homolog gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23023706 62287 Pten phosphatase and tensin homolog gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18463637 62287 Pten phosphatase and tensin homolog gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9697695 62287 Pten phosphatase and tensin homolog gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 62287 Pten phosphatase and tensin homolog gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16818619 62287 Pten phosphatase and tensin homolog gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9799734 62287 Pten phosphatase and tensin homolog gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19879843 62287 Pten phosphatase and tensin homolog gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14691534 62287 Pten phosphatase and tensin homolog gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15492213 62287 Pten phosphatase and tensin homolog gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23023706 62287 Pten phosphatase and tensin homolog gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18239123 62287 Pten phosphatase and tensin homolog gene MP:0011122 absent primordial ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:18239123 62287 Pten phosphatase and tensin homolog gene MP:0011139 increased lung endothelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19574443 62287 Pten phosphatase and tensin homolog gene MP:0011142 abnormal lung-associated mesenchyme development IAGP N RGD:5509061 20141003 MGI PMID:23023706 62287 Pten phosphatase and tensin homolog gene MP:0011147 increased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20170119 MGI PMID:27573812 62287 Pten phosphatase and tensin homolog gene MP:0011237 decreased blood oxygen capacity IAGP N RGD:5509061 20141003 MGI PMID:23023706 62287 Pten phosphatase and tensin homolog gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20141003 MGI PMID:18497742 62287 Pten phosphatase and tensin homolog gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:17540362 62287 Pten phosphatase and tensin homolog gene MP:0011336 abnormal kidney pelvis urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18497742 62287 Pten phosphatase and tensin homolog gene MP:0011403 pyelonephritis IAGP N RGD:5509061 20141003 MGI PMID:17607361 62287 Pten phosphatase and tensin homolog gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18497742 62287 Pten phosphatase and tensin homolog gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20210826 MGI PMID:29969932 62287 Pten phosphatase and tensin homolog gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0011766 abnormal urinary bladder mucosa morphology IAGP N RGD:5509061 20160915 MGI PMID:21283818 62287 Pten phosphatase and tensin homolog gene MP:0011789 increased urethra carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16488991 62287 Pten phosphatase and tensin homolog gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20150611 MGI PMID:16537919 62287 Pten phosphatase and tensin homolog gene MP:0011874 enlarged urinary bladder IAGP N RGD:5509061 20160915 MGI PMID:21283818 62287 Pten phosphatase and tensin homolog gene MP:0012043 increased myoepithelioma incidence IAGP N RGD:5509061 20160331 MGI PMID:25330770 62287 Pten phosphatase and tensin homolog gene MP:0012065 increased astrocyte number IAGP N RGD:5509061 20150430 MGI PMID:24470394 62287 Pten phosphatase and tensin homolog gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20210826 MGI PMID:28636948 62287 Pten phosphatase and tensin homolog gene MP:0012319 fast extinction of fear memory IAGP N RGD:5509061 20210826 MGI PMID:28636948 62287 Pten phosphatase and tensin homolog gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18687666 62287 Pten phosphatase and tensin homolog gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19237610 62287 Pten phosphatase and tensin homolog gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21860425 62287 Pten phosphatase and tensin homolog gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22214849 62287 Pten phosphatase and tensin homolog gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20160204 MGI PMID:25815421 62287 Pten phosphatase and tensin homolog gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20160811 MGI PMID:26061565 62287 Pten phosphatase and tensin homolog gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10910075 62287 Pten phosphatase and tensin homolog gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15492213 62287 Pten phosphatase and tensin homolog gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19011632 62287 Pten phosphatase and tensin homolog gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20194734 62287 Pten phosphatase and tensin homolog gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20956547 62287 Pten phosphatase and tensin homolog gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21493594 62287 Pten phosphatase and tensin homolog gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9990064 62287 Pten phosphatase and tensin homolog gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20170706 MGI PMID:28162974 62287 Pten phosphatase and tensin homolog gene MP:0012432 decreased prostate gland tumor incidence IAGP N RGD:5509061 20181004 MGI PMID:29720449 62287 Pten phosphatase and tensin homolog gene MP:0012433 decreased ovarian tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20505730 62287 Pten phosphatase and tensin homolog gene MP:0012459 increased dentate gyrus size IAGP N RGD:5509061 20150917 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0012550 respiratory acidosis IAGP N RGD:5509061 20170921 MGI PMID:17909629 62287 Pten phosphatase and tensin homolog gene MP:0012570 increased mammary gland tumor incidence in breeding females IAGP N RGD:5509061 20160331 MGI PMID:25330770 62287 Pten phosphatase and tensin homolog gene MP:0012674 tomacula IAGP N RGD:5509061 20170629 MGI PMID:27504968 62287 Pten phosphatase and tensin homolog gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20141003 MGI PMID:22214849 62287 Pten phosphatase and tensin homolog gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20160714 MGI PMID:17418409 62287 Pten phosphatase and tensin homolog gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20181129 MGI PMID:27032374 62287 Pten phosphatase and tensin homolog gene MP:0013218 abnormal substantia nigra pars reticulata morphology IAGP N RGD:5509061 20141003 MGI PMID:19750226 62287 Pten phosphatase and tensin homolog gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20141003 MGI PMID:19750226 62287 Pten phosphatase and tensin homolog gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20141120 MGI PMID:20807812 62287 Pten phosphatase and tensin homolog gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20160128 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0013399 endometrium fibrosis IAGP N RGD:5509061 20141218 MGI PMID:20858757 62287 Pten phosphatase and tensin homolog gene MP:0013693 abnormal hemopoiesis IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0014038 increased hepatocyte number IAGP N RGD:5509061 20160304 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0014045 Mallory bodies IAGP N RGD:5509061 20160304 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0014045 Mallory bodies IAGP N RGD:5509061 20160304 MGI PMID:17567478 62287 Pten phosphatase and tensin homolog gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20210826 MGI PMID:29969932 62287 Pten phosphatase and tensin homolog gene MP:0014049 increased T cell acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20160818 MGI PMID:26764354 62287 Pten phosphatase and tensin homolog gene MP:0014081 branched small intestinal villi IAGP N RGD:5509061 20160414 MGI PMID:19168705 62287 Pten phosphatase and tensin homolog gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:17418409 62287 Pten phosphatase and tensin homolog gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:17607361 62287 Pten phosphatase and tensin homolog gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:18043744 62287 Pten phosphatase and tensin homolog gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:19196966 62287 Pten phosphatase and tensin homolog gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:21860425 62287 Pten phosphatase and tensin homolog gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:22341455 62287 Pten phosphatase and tensin homolog gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:22796458 62287 Pten phosphatase and tensin homolog gene MP:0014373 increased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:22302806 62287 Pten phosphatase and tensin homolog gene MP:0014375 increased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:22302806 62287 Pten phosphatase and tensin homolog gene MP:0014395 increased myocardial fiber mitochondrial DNA content IAGP N RGD:5509061 20240328 MGI PMID:29969932 62287 Pten phosphatase and tensin homolog gene MP:0020410 increased liposarcoma incidence IAGP N RGD:5509061 20180111 MGI PMID:27573812 62287 Pten phosphatase and tensin homolog gene MP:0020507 increased dendritic spine density IAGP N RGD:5509061 20211014 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0020507 increased dendritic spine density IAGP N RGD:5509061 20211014 MGI PMID:22302806 62287 Pten phosphatase and tensin homolog gene MP:0030574 increased hair follicle cell proliferation IAGP N RGD:5509061 20181129 MGI PMID:16204035 62287 Pten phosphatase and tensin homolog gene MP:0030736 increased glutamic acid level IAGP N RGD:5509061 20210826 MGI PMID:31291551 62287 Pten phosphatase and tensin homolog gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:22341455 62287 Pten phosphatase and tensin homolog gene MP:0030928 increased telomere length IAGP N RGD:5509061 20190117 MGI PMID:22341455 62287 Pten phosphatase and tensin homolog gene MP:0030951 abnormal endocytosis IAGP N RGD:5509061 20210826 MGI PMID:31291551 62287 Pten phosphatase and tensin homolog gene MP:0031016 decreased granulosa cell apoptosis IAGP N RGD:5509061 20200130 MGI PMID:18606860 62287 Pten phosphatase and tensin homolog gene MP:0031016 decreased granulosa cell apoptosis IAGP N RGD:5509061 20200130 MGI PMID:21860425 62287 Pten phosphatase and tensin homolog gene MP:0031019 increased granulosa cell proliferation IAGP N RGD:5509061 20200130 MGI PMID:18606860 62287 Pten phosphatase and tensin homolog gene MP:0031019 increased granulosa cell proliferation IAGP N RGD:5509061 20200130 MGI PMID:21860425 62287 Pten phosphatase and tensin homolog gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20200130 MGI PMID:18239123 62287 Pten phosphatase and tensin homolog gene MP:0031080 pulmonary embolism IAGP N RGD:5509061 20200709 MGI PMID:18687666 62287 Pten phosphatase and tensin homolog gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21479224 62287 Pten phosphatase and tensin homolog gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:15199412 62287 Pten phosphatase and tensin homolog gene MP:0031217 increased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20210826 MGI PMID:29969932 62287 Pten phosphatase and tensin homolog gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:20200318 62287 Pten phosphatase and tensin homolog gene MP:0031369 prostate gland dorsolateral lobe hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:14691534 62287 Pten phosphatase and tensin homolog gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:16675393 62287 Pten phosphatase and tensin homolog gene MP:0031421 increased superovulation rate IAGP N RGD:5509061 20220714 MGI PMID:18606860 62287 Pten phosphatase and tensin homolog gene MP:0031423 abnormal luteolysis IAGP N RGD:5509061 20220714 MGI PMID:18606860 62287 Pten phosphatase and tensin homolog gene MP:0031424 enhanced female fertility IAGP N RGD:5509061 20220714 MGI PMID:18606860 62287 Pten phosphatase and tensin homolog gene MP:0031587 abnormal pericardium development IAGP N RGD:5509061 20240229 MGI PMID:16818619 62288 F2 coagulation factor II gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:9636195 62288 F2 coagulation factor II gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0000745 tremors IEA N RGD:5509061 20170105 MGI 62288 F2 coagulation factor II gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 62288 F2 coagulation factor II gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:21436072 62288 F2 coagulation factor II gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9636195 62288 F2 coagulation factor II gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:9636195 62288 F2 coagulation factor II gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:9636195 62288 F2 coagulation factor II gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9636195 62288 F2 coagulation factor II gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9636195 62288 F2 coagulation factor II gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9636196 62288 F2 coagulation factor II gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9636196 62288 F2 coagulation factor II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 62288 F2 coagulation factor II gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 62288 F2 coagulation factor II gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9636196 62288 F2 coagulation factor II gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:21436072 62288 F2 coagulation factor II gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:9636196 62288 F2 coagulation factor II gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 62288 F2 coagulation factor II gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:9636195 62288 F2 coagulation factor II gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:21436072 62288 F2 coagulation factor II gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:21436072 62288 F2 coagulation factor II gene MP:0006052 cerebellum hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:21436072 62288 F2 coagulation factor II gene MP:0008816 petechiae IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 62288 F2 coagulation factor II gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 62288 F2 coagulation factor II gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 62288 F2 coagulation factor II gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9636196 62288 F2 coagulation factor II gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21436072 62288 F2 coagulation factor II gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9636195 62288 F2 coagulation factor II gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9636195 62288 F2 coagulation factor II gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9636196 62288 F2 coagulation factor II gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9636196 62288 F2 coagulation factor II gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9636195 62288 F2 coagulation factor II gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9636196 62288 F2 coagulation factor II gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 62288 F2 coagulation factor II gene MP:0011514 skin hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0011515 purpura IAGP N RGD:5509061 20141003 MGI PMID:9636195 62288 F2 coagulation factor II gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:9636195 62288 F2 coagulation factor II gene MP:0020215 impaired blood coagulation IAGP N RGD:5509061 20200625 MGI PMID:9636195 62288 F2 coagulation factor II gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201001 MGI PMID:21436072 62288 F2 coagulation factor II gene MP:0031136 muscle hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0031138 testicular hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:18927430 62288 F2 coagulation factor II gene MP:0031152 subcutaneous hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:21436072 62288 F2 coagulation factor II gene MP:0031154 intestinal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:9636195 62289 Kcnk3 potassium channel, subfamily K, member 3 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:18250325 62289 Kcnk3 potassium channel, subfamily K, member 3 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:16339039 62289 Kcnk3 potassium channel, subfamily K, member 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141106 MGI 62289 Kcnk3 potassium channel, subfamily K, member 3 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:18250325 62289 Kcnk3 potassium channel, subfamily K, member 3 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:22918120 62289 Kcnk3 potassium channel, subfamily K, member 3 gene MP:0002909 abnormal adrenal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:18250325 62289 Kcnk3 potassium channel, subfamily K, member 3 gene MP:0003353 decreased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:18250325 62289 Kcnk3 potassium channel, subfamily K, member 3 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:18250325 62289 Kcnk3 potassium channel, subfamily K, member 3 gene MP:0004119 hypokalemia IAGP N RGD:5509061 20141003 MGI PMID:18250325 62289 Kcnk3 potassium channel, subfamily K, member 3 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:18250325 62289 Kcnk3 potassium channel, subfamily K, member 3 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:18094244 62290 Ywhab tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 62290 Ywhab tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 62290 Ywhab tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20200514 MGI 62290 Ywhab tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20200514 MGI 62290 Ywhab tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210520 MGI 62290 Ywhab tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200514 MGI 62290 Ywhab tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20220825 MGI PMID:33641163 62290 Ywhab tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20200514 MGI 62290 Ywhab tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20220825 MGI PMID:33641163 62290 Ywhab tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 62290 Ywhab tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20200514 MGI 62290 Ywhab tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20200514 MGI 62290 Ywhab tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20220825 MGI PMID:33641163 62290 Ywhab tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 62290 Ywhab tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta polypeptide gene MP:0030974 enhanced gluconeogenesis IAGP N RGD:5509061 20220825 MGI PMID:33641163 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23071090 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:23071090 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0000373 belly spot IAGP N RGD:5509061 20181227 MGI PMID:27001213 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12796778 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:12796778 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20181227 MGI PMID:27001213 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:23071090 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0001926 female infertility IAGP N RGD:5509061 20191226 MGI PMID:31640562 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23071090 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20181227 MGI PMID:27001213 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12796778 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:23071090 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:23071090 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23071090 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:23071090 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:23071090 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23071090 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12796778 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:23071090 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:12796778 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20181227 MGI PMID:27001213 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23071090 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:23071090 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23071090 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12796778 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20181227 MGI PMID:27001213 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23071090 62292 Ywhae tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23071090 62293 Muc5ac mucin 5, subtypes A and C, tracheobronchial/gastric gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:23272068 62293 Muc5ac mucin 5, subtypes A and C, tracheobronchial/gastric gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21502330 62293 Muc5ac mucin 5, subtypes A and C, tracheobronchial/gastric gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:21502330 62293 Muc5ac mucin 5, subtypes A and C, tracheobronchial/gastric gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:23272068 62293 Muc5ac mucin 5, subtypes A and C, tracheobronchial/gastric gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:21502330 62293 Muc5ac mucin 5, subtypes A and C, tracheobronchial/gastric gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 62293 Muc5ac mucin 5, subtypes A and C, tracheobronchial/gastric gene MP:0012164 abnormal conjunctiva goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23272068 62294 Ywhag tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma polypeptide gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15684385 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16944268 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0000424 retarded hair growth IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:19629164 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17124323 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17124323 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001345 Meibomian gland atrophy IAGP N RGD:5509061 20240502 MGI PMID:37117756 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001391 abnormal tail movements IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18413500 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22697126 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:16944268 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:20562852 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:17360665 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:19056819 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:23267082 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19056819 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15523558 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16944268 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17124323 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15523558 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16925591 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20240404 MGI PMID:33055157 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002607 decreased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:18413500 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15523558 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20141003 MGI PMID:22697126 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:16944268 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20562852 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003198 calcified tendon IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003200 calcified joint IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:11163178 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:17124323 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003415 priapism IAGP N RGD:5509061 20141003 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20562852 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:16925591 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0004622 sacral vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0004685 calcified intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17360665 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18413500 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:16143109 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:16143109 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:16143109 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16925591 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16944268 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16925591 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16944268 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:18413500 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:19056819 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20562852 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17360665 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:16944268 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:18413500 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005489 vascular smooth muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005504 abnormal ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:16944268 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17719549 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16944268 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16944268 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20240502 MGI PMID:37117756 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005626 decreased plasma anion gap IAGP N RGD:5509061 20141003 MGI PMID:16944268 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005660 abnormal circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:17360665 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005661 decreased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:17360665 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0005664 decreased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:17360665 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0006432 abnormal costal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:16925591 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:16925591 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20171012 MGI PMID:18413500 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16925591 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20141003 MGI PMID:19629164 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16143109 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:19056819 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:20562852 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0009436 fragmentation of sleep/wake states IAGP N RGD:5509061 20141003 MGI PMID:16944268 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20240404 MGI PMID:33055157 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0010686 abnormal hair follicle matrix region morphology IAGP N RGD:5509061 20141003 MGI PMID:19629164 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0011021 abnormal circadian regulation of heart rate IAGP N RGD:5509061 20141003 MGI PMID:17360665 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0011022 abnormal circadian regulation of systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17360665 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0012008 delayed parturition IAGP N RGD:5509061 20191219 MGI PMID:22697126 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0012009 early parturition IAGP N RGD:5509061 20191219 MGI PMID:22697126 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0012329 increased circulating factor VIII level IAGP N RGD:5509061 20210204 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0012331 increased circulating fibrinogen level IAGP N RGD:5509061 20200618 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0012355 decreased prothrombin time IAGP N RGD:5509061 20200917 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0012359 increased partial thromboplastin time IAGP N RGD:5509061 20200917 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0013373 increased sebum secretion IAGP N RGD:5509061 20150205 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0014167 ectopic bone IAGP N RGD:5509061 20160407 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:17124323 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:17360665 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:17719549 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:21921292 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:22697126 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:17124323 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:21921292 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:11163178 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:11163178 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0020475 delayed circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:21966515 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20171012 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0020478 abnormal circadian sleep/wake cycle IAGP N RGD:5509061 20171012 MGI PMID:16944268 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0020857 cornea epithelium hyperplasia IAGP N RGD:5509061 20181101 MGI PMID:16847346 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0030776 calcified calcaneal tendon IAGP N RGD:5509061 20181004 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0030776 calcified calcaneal tendon IAGP N RGD:5509061 20181004 MGI PMID:17124323 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0030837 abnormal knee joint morphology IAGP N RGD:5509061 20181025 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0030973 impaired gluconeogenesis IAGP N RGD:5509061 20200102 MGI PMID:15523558 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0030984 increased circulating osteocalcin level IAGP N RGD:5509061 20200618 MGI PMID:15739187 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0031158 abnormal venous thrombosis IAGP N RGD:5509061 20201119 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0031214 hypercoagulability IAGP N RGD:5509061 20201231 MGI PMID:21799179 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0031269 increased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:21966465 62295 Bmal1 basic helix-loop-helix ARNT like 1 gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:21966465 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0000448 pointed snout IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17287346 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17287346 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17287346 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:17287346 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:17287346 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:17287346 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17287346 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0030273 mandibular retrognathia IAGP N RGD:5509061 20171026 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:8494785 62296 Cask calcium/calmodulin dependent serine protein kinase gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:8494785 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230629 MGI PMID:28408410 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23870131 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23870131 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230629 MGI PMID:28408410 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20230629 MGI PMID:28408410 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20230629 MGI PMID:28408410 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230629 MGI PMID:28408410 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160804 MGI 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0002083 premature death IAGP N RGD:5509061 20230629 MGI PMID:28408410 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20230629 MGI PMID:28408410 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23870131 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0005352 small cranium IAGP N RGD:5509061 20230629 MGI PMID:28408410 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160804 MGI 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23870131 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23870131 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20230629 MGI PMID:28408410 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20230629 MGI PMID:28408410 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0020337 abnormal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20230629 MGI PMID:28408410 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20230629 MGI PMID:28408410 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0020510 increased dendritic spine length IAGP N RGD:5509061 20230629 MGI PMID:28408410 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0020512 abnormal dendritic mushroom spine morphology IAGP N RGD:5509061 20230629 MGI PMID:28408410 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0020514 abnormal dendritic thin spine morphology IAGP N RGD:5509061 20230629 MGI PMID:28408410 62298 Smc3 structural maintenance of chromosomes 3 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20230629 MGI PMID:28408410 62299 Ensa endosulfine alpha gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 62299 Ensa endosulfine alpha gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 62299 Ensa endosulfine alpha gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220519 MGI 62299 Ensa endosulfine alpha gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220519 MGI 62299 Ensa endosulfine alpha gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20220811 MGI 62299 Ensa endosulfine alpha gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20191205 MGI PMID:30626720 62300 Cntn6 contactin 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12884264 62300 Cntn6 contactin 6 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18046458 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:8978608 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170706 MGI PMID:28275192 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:8978608 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:8978608 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8978608 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0005363 decreased susceptibility to prion infection IAGP N RGD:5509061 20170706 MGI PMID:28275192 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10917533 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0008200 decreased follicular dendritic cell number IAGP N RGD:5509061 20170706 MGI PMID:28275192 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0008201 absent follicular dendritic cells IAGP N RGD:5509061 20141003 MGI PMID:10917533 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0008471 abnormal spleen primary B follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:8978608 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0008472 abnormal spleen secondary B follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:8978608 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:8978608 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10917533 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8978608 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0009628 absent brachial lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10917533 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10917533 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0009633 absent cervical lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10917533 62302 Cxcr5 C-X-C motif chemokine receptor 5 gene MP:0010740 abnormal dendritic cell chemotaxis IAGP N RGD:5509061 20170706 MGI PMID:28275192 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:12811850 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:15499020 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16516168 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16516168 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:11809737 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12811850 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11809737 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11809737 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:11809737 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11809737 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12811850 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12811850 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11809737 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:11809737 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11809737 62303 Igbp1 immunoglobulin (CD79A) binding protein 1 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:12811850 62304 Syt6 synaptotagmin VI gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 62305 Syt7 synaptotagmin VII gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20211021 MGI 62305 Syt7 synaptotagmin VII gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12925704 62305 Syt7 synaptotagmin VII gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 62305 Syt7 synaptotagmin VII gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 62305 Syt7 synaptotagmin VII gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12925704 62305 Syt7 synaptotagmin VII gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:12925704 62305 Syt7 synaptotagmin VII gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 62305 Syt7 synaptotagmin VII gene MP:0002915 abnormal synaptic depression IAGP N RGD:5509061 20241031 MGI PMID:33753311 62305 Syt7 synaptotagmin VII gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12925704 62305 Syt7 synaptotagmin VII gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:12925704 62305 Syt7 synaptotagmin VII gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:12925704 62305 Syt7 synaptotagmin VII gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20241031 MGI PMID:33753311 62305 Syt7 synaptotagmin VII gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 62305 Syt7 synaptotagmin VII gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:12925704 62305 Syt7 synaptotagmin VII gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12925704 62305 Syt7 synaptotagmin VII gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12925704 62305 Syt7 synaptotagmin VII gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:12925704 62305 Syt7 synaptotagmin VII gene MP:0014253 decreased paired-pulse ratio IAGP N RGD:5509061 20241031 MGI PMID:33753311 62305 Syt7 synaptotagmin VII gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20221215 MGI 62306 Nxf1 nuclear RNA export factor 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19436707 62306 Nxf1 nuclear RNA export factor 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9182797 62306 Nxf1 nuclear RNA export factor 1 gene MP:0000745 tremors IAGP N RGD:5509061 20150430 MGI PMID:25835743 62306 Nxf1 nuclear RNA export factor 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19436707 62306 Nxf1 nuclear RNA export factor 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:14517553 62306 Nxf1 nuclear RNA export factor 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:14517553 62306 Nxf1 nuclear RNA export factor 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:19436707 62306 Nxf1 nuclear RNA export factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14517553 62306 Nxf1 nuclear RNA export factor 1 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:14517553 62306 Nxf1 nuclear RNA export factor 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:14517553 62306 Nxf1 nuclear RNA export factor 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:19436707 62306 Nxf1 nuclear RNA export factor 1 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20150430 MGI PMID:25835743 62306 Nxf1 nuclear RNA export factor 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:14517553 62307 Nfib nuclear factor I/B gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:21513708 62307 Nfib nuclear factor I/B gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:21513708 62307 Nfib nuclear factor I/B gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:21513708 62307 Nfib nuclear factor I/B gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0003005 abnormal hippocampal fimbria morphology IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0003792 abnormal major salivary gland morphology IAGP N RGD:5509061 20150806 MGI PMID:25403566 62307 Nfib nuclear factor I/B gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:21931569 62307 Nfib nuclear factor I/B gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17553984 62307 Nfib nuclear factor I/B gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:21931569 62307 Nfib nuclear factor I/B gene MP:0004882 enlarged lung IAGP N RGD:5509061 20141003 MGI PMID:21513708 62307 Nfib nuclear factor I/B gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0008268 absent hippocampus CA3 region IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0009520 decreased submandibular gland size IAGP N RGD:5509061 20150806 MGI PMID:25403566 62307 Nfib nuclear factor I/B gene MP:0009522 submandibular gland hypoplasia IAGP N RGD:5509061 20150806 MGI PMID:25403566 62307 Nfib nuclear factor I/B gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:21513708 62307 Nfib nuclear factor I/B gene MP:0010826 absent lung saccules IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0010826 absent lung saccules IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0010827 small lung saccule IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0011032 impaired branching involved in terminal bronchiole morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20150806 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21513708 62307 Nfib nuclear factor I/B gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0011163 increased wet-to-dry lung weight ratio IAGP N RGD:5509061 20141003 MGI PMID:11850179 62307 Nfib nuclear factor I/B gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:15632069 62307 Nfib nuclear factor I/B gene MP:0013541 abnormal submandibular gland development IAGP N RGD:5509061 20150806 MGI PMID:25403566 62308 Nfic nuclear factor I/C gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:12529411 62308 Nfic nuclear factor I/C gene MP:0000126 brittle teeth IAGP N RGD:5509061 20171228 MGI PMID:12529411 62308 Nfic nuclear factor I/C gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12529411 62308 Nfic nuclear factor I/C gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:12529411 62308 Nfic nuclear factor I/C gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12529411 62308 Nfic nuclear factor I/C gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:12529411 62308 Nfic nuclear factor I/C gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20141003 MGI PMID:12529411 62308 Nfic nuclear factor I/C gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:12529411 62308 Nfic nuclear factor I/C gene MP:0004791 absent lower incisors IAGP N RGD:5509061 20141003 MGI PMID:12529411 62308 Nfic nuclear factor I/C gene MP:0011165 abnormal tooth root development IAGP N RGD:5509061 20141003 MGI PMID:12529411 62308 Nfic nuclear factor I/C gene MP:0011166 absent molar root IAGP N RGD:5509061 20141003 MGI PMID:12529411 62308 Nfic nuclear factor I/C gene MP:0030083 long upper incisors IAGP N RGD:5509061 20170928 MGI PMID:12529411 62308 Nfic nuclear factor I/C gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:12529411 62308 Nfic nuclear factor I/C gene MP:0030137 abnormal upper incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:12529411 62308 Nfic nuclear factor I/C gene MP:0030489 abnormal molar socket morphology IAGP N RGD:5509061 20171228 MGI PMID:12529411 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200402 MGI 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20200402 MGI 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0000692 small spleen IEA N RGD:5509061 20200402 MGI 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20200402 MGI 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20200402 MGI 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:17292798 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20200402 MGI 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20181227 MGI 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0002989 small kidney IEA N RGD:5509061 20200402 MGI 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0003476 decreased summary potential intensity IAGP N RGD:5509061 20200903 MGI PMID:31661900 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20220519 MGI 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20200402 MGI 62309 Pebp1 phosphatidylethanolamine binding protein 1 gene MP:0011150 abnormal hippocampus stratum oriens morphology IAGP N RGD:5509061 20200903 MGI PMID:31661900 62310 Ppp1r1a protein phosphatase 1, regulatory inhibitor subunit 1A gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10804194 62311 Clip2 CAP-GLY domain containing linker protein 2 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12195424 62311 Clip2 CAP-GLY domain containing linker protein 2 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:12195424 62311 Clip2 CAP-GLY domain containing linker protein 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12195424 62311 Clip2 CAP-GLY domain containing linker protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12195424 62311 Clip2 CAP-GLY domain containing linker protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12195424 62311 Clip2 CAP-GLY domain containing linker protein 2 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12195424 62311 Clip2 CAP-GLY domain containing linker protein 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12195424 62311 Clip2 CAP-GLY domain containing linker protein 2 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:12195424 62311 Clip2 CAP-GLY domain containing linker protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12195424 62311 Clip2 CAP-GLY domain containing linker protein 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12195424 62311 Clip2 CAP-GLY domain containing linker protein 2 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:12195424 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20221117 MGI PMID:29986157 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20221117 MGI PMID:29986157 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0000435 shortened head IAGP N RGD:5509061 20221117 MGI PMID:29986157 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20220811 MGI PMID:34360715 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220811 MGI PMID:34360715 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0001710 absent amniotic folds IAGP N RGD:5509061 20141003 MGI PMID:10848611 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10848611 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220811 MGI PMID:34360715 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20230615 MGI PMID:28655788 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:10848611 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230615 MGI PMID:28655788 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0004380 short frontal bone IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0004540 small maxilla IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20221117 MGI PMID:29986157 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0004830 short incisors IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0004870 small premaxilla IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220811 MGI PMID:34360715 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20141003 MGI 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20220811 MGI PMID:34360715 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20221117 MGI PMID:29986157 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20141003 MGI PMID:10848611 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20230615 MGI PMID:28655788 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221117 MGI PMID:29986157 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20221117 MGI PMID:29986157 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221117 MGI PMID:29986157 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10848611 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19289494 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0011198 absent proamniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:10848611 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0011207 absent ectoplacental cavity IAGP N RGD:5509061 20141003 MGI PMID:10848611 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220811 MGI PMID:34360715 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230615 MGI PMID:28655788 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0020301 short tongue IAGP N RGD:5509061 20221117 MGI PMID:29986157 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20221117 MGI PMID:29986157 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:29986157 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:29986157 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0030089 short lower incisors IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0030090 short upper incisors IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0030431 wide metopic suture IAGP N RGD:5509061 20221215 MGI PMID:29727702 62312 Prmt1 protein arginine N-methyltransferase 1 gene MP:0031278 decreased osteosarcoma incidence IAGP N RGD:5509061 20230615 MGI PMID:28655788 62315 Camkk1 calcium/calmodulin-dependent protein kinase kinase 1, alpha gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17015467 62315 Camkk1 calcium/calmodulin-dependent protein kinase kinase 1, alpha gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19864584 62315 Camkk1 calcium/calmodulin-dependent protein kinase kinase 1, alpha gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19864584 62316 Rps12 ribosomal protein S12 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0000585 kinked tail IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0002083 premature death IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62316 Rps12 ribosomal protein S12 gene MP:0011176 abnormal erythroblast morphology IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20231130 MGI PMID:37272618 62316 Rps12 ribosomal protein S12 gene MP:0011901 abnormal hematopoietic stem cell proliferation IAGP N RGD:5509061 20231130 MGI PMID:37272618 62317 Rps14 ribosomal protein S14 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180426 MGI PMID:26878232 62317 Rps14 ribosomal protein S14 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20180426 MGI PMID:26878232 62317 Rps14 ribosomal protein S14 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20180426 MGI PMID:26878232 62317 Rps14 ribosomal protein S14 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20180426 MGI PMID:26878232 62317 Rps14 ribosomal protein S14 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20180426 MGI PMID:26878232 62317 Rps14 ribosomal protein S14 gene MP:0003405 abnormal platelet shape IAGP N RGD:5509061 20180426 MGI PMID:26878232 62317 Rps14 ribosomal protein S14 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20180426 MGI PMID:26878232 62317 Rps14 ribosomal protein S14 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20180426 MGI PMID:26878232 62317 Rps14 ribosomal protein S14 gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20180426 MGI PMID:26878232 62317 Rps14 ribosomal protein S14 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20180426 MGI PMID:26878232 62317 Rps14 ribosomal protein S14 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20180426 MGI PMID:26878232 62317 Rps14 ribosomal protein S14 gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:26878232 62322 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20191003 MGI PMID:31147515 62322 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20151112 MGI PMID:26241864 62322 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20191003 MGI PMID:31147515 62322 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta gene MP:0002833 increased heart weight IAGP N RGD:5509061 20151112 MGI PMID:26241864 62322 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20191003 MGI PMID:31147515 62322 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20191003 MGI PMID:31147515 62322 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20151112 MGI PMID:26241864 62322 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20151112 MGI PMID:26241864 62322 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20191003 MGI PMID:31147515 62322 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20191003 MGI PMID:31147515 62322 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20151112 MGI PMID:26241864 62322 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:26241864 62323 Coil coilin gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:11470819 62323 Coil coilin gene MP:0008888 abnormal Cajal body morphology IAGP N RGD:5509061 20141003 MGI PMID:11470819 62324 Adam7 a disintegrin and metallopeptidase domain 7 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20161103 MGI PMID:26246218 62324 Adam7 a disintegrin and metallopeptidase domain 7 gene MP:0001293 anophthalmia IEA N RGD:5509061 20240523 MGI 62324 Adam7 a disintegrin and metallopeptidase domain 7 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20161103 MGI PMID:26246218 62324 Adam7 a disintegrin and metallopeptidase domain 7 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 62324 Adam7 a disintegrin and metallopeptidase domain 7 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20161103 MGI PMID:26246218 62324 Adam7 a disintegrin and metallopeptidase domain 7 gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20161103 MGI PMID:26246218 62324 Adam7 a disintegrin and metallopeptidase domain 7 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20161103 MGI PMID:26246218 62324 Adam7 a disintegrin and metallopeptidase domain 7 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20161103 MGI PMID:26246218 62324 Adam7 a disintegrin and metallopeptidase domain 7 gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20161103 MGI PMID:26246218 62324 Adam7 a disintegrin and metallopeptidase domain 7 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20161103 MGI PMID:26246218 62324 Adam7 a disintegrin and metallopeptidase domain 7 gene MP:0009824 spermatic granuloma IAGP N RGD:5509061 20161103 MGI PMID:26246218 62325 Npff neuropeptide FF-amide peptide precursor gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 62327 Cd37 CD37 antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:10891477 62327 Cd37 CD37 antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:10891477 62327 Cd37 CD37 antigen gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:10891477 62327 Cd37 CD37 antigen gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:10891477 62327 Cd37 CD37 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:10891477 62327 Cd37 CD37 antigen gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:10891477 62328 Fdx1 ferredoxin 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 62328 Fdx1 ferredoxin 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 62328 Fdx1 ferredoxin 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 62328 Fdx1 ferredoxin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17088210 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17088210 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17088210 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17088210 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:10727859 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10727859 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:10727859 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0001705 abnormal proximal-distal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10727859 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10727859 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16873068 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:10727859 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:17088210 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17088213 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17088210 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:17088210 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:16873068 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:10727859 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10727859 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:10727859 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0004264 abnormal extraembryonic tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:10727859 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17088213 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20200402 MGI PMID:31151856 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20200402 MGI PMID:31151856 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20200402 MGI PMID:31151856 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10727859 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10727859 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10727859 62329 Arc activity regulated cytoskeletal-associated protein gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:17088210 62330 Dctn1 dynactin 1 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:18094236 62330 Dctn1 dynactin 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20181018 MGI PMID:29490687 62330 Dctn1 dynactin 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:18094236 62330 Dctn1 dynactin 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20181018 MGI PMID:29490687 62330 Dctn1 dynactin 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20181018 MGI PMID:29490687 62330 Dctn1 dynactin 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:18094236 62330 Dctn1 dynactin 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20181018 MGI PMID:29490687 62330 Dctn1 dynactin 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20181018 MGI PMID:29490687 62330 Dctn1 dynactin 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:18094236 62330 Dctn1 dynactin 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20181018 MGI PMID:29490687 62330 Dctn1 dynactin 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:18094236 62330 Dctn1 dynactin 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18094236 62330 Dctn1 dynactin 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18094236 62330 Dctn1 dynactin 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20181018 MGI PMID:29490687 62330 Dctn1 dynactin 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20181018 MGI PMID:29490687 62330 Dctn1 dynactin 1 gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20181018 MGI PMID:29490687 62330 Dctn1 dynactin 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210128 MGI 62330 Dctn1 dynactin 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18094236 62330 Dctn1 dynactin 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:18094236 62330 Dctn1 dynactin 1 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20181018 MGI PMID:29490687 62330 Dctn1 dynactin 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20181018 MGI PMID:29490687 62330 Dctn1 dynactin 1 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20181018 MGI PMID:29490687 62330 Dctn1 dynactin 1 gene MP:0009422 decreased gastrocnemius weight IAGP N RGD:5509061 20181018 MGI PMID:29490687 62330 Dctn1 dynactin 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18094236 62330 Dctn1 dynactin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62331 Plk3 polo like kinase 3 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18519666 62331 Plk3 polo like kinase 3 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18519666 62331 Plk3 polo like kinase 3 gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18519666 62331 Plk3 polo like kinase 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:21376736 62331 Plk3 polo like kinase 3 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:18519666 62331 Plk3 polo like kinase 3 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:18519666 62331 Plk3 polo like kinase 3 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:21376736 62331 Plk3 polo like kinase 3 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:21376736 62331 Plk3 polo like kinase 3 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18519666 62331 Plk3 polo like kinase 3 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18519666 62331 Plk3 polo like kinase 3 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20231102 MGI PMID:24128992 62332 Hpx hemopexin gene MP:0000315 hemoglobinuria IAGP N RGD:5509061 20141003 MGI PMID:10572107 62332 Hpx hemopexin gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12393471 62332 Hpx hemopexin gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:12393471 62332 Hpx hemopexin gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:10572107 62332 Hpx hemopexin gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10572107 62332 Hpx hemopexin gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:12393471 62332 Hpx hemopexin gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:12393471 62332 Hpx hemopexin gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12393471 62332 Hpx hemopexin gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12393471 62332 Hpx hemopexin gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20141003 MGI PMID:10572107 62332 Hpx hemopexin gene MP:0012666 increased circulating haptoglobin level IAGP N RGD:5509061 20141003 MGI PMID:10572107 62333 Syt10 synaptotagmin X gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 62333 Syt10 synaptotagmin X gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:21921292 62333 Syt10 synaptotagmin X gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:21921292 62333 Syt10 synaptotagmin X gene MP:0020474 advanced circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:21921292 62334 Syt11 synaptotagmin XI gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 62335 Xdh xanthine dehydrogenase gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20190808 MGI PMID:23024809 62335 Xdh xanthine dehydrogenase gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20190808 MGI PMID:23024809 62335 Xdh xanthine dehydrogenase gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:15528468 62335 Xdh xanthine dehydrogenase gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12502743 62335 Xdh xanthine dehydrogenase gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20220519 MGI 62335 Xdh xanthine dehydrogenase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12502743 62335 Xdh xanthine dehydrogenase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12502743 62335 Xdh xanthine dehydrogenase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 62335 Xdh xanthine dehydrogenase gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 62335 Xdh xanthine dehydrogenase gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:12502743 62335 Xdh xanthine dehydrogenase gene MP:0001925 male infertility IEA N RGD:5509061 20220519 MGI 62335 Xdh xanthine dehydrogenase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 62335 Xdh xanthine dehydrogenase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12502743 62335 Xdh xanthine dehydrogenase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0002083 premature death IAGP N RGD:5509061 20190808 MGI PMID:23024809 62335 Xdh xanthine dehydrogenase gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:15528468 62335 Xdh xanthine dehydrogenase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 62335 Xdh xanthine dehydrogenase gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20190808 MGI PMID:23024809 62335 Xdh xanthine dehydrogenase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:15528468 62335 Xdh xanthine dehydrogenase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20190808 MGI PMID:23024809 62335 Xdh xanthine dehydrogenase gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20190808 MGI PMID:23024809 62335 Xdh xanthine dehydrogenase gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:15528468 62335 Xdh xanthine dehydrogenase gene MP:0002989 small kidney IAGP N RGD:5509061 20190808 MGI PMID:23024809 62335 Xdh xanthine dehydrogenase gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20190808 MGI PMID:23024809 62335 Xdh xanthine dehydrogenase gene MP:0003432 increased activity of parathyroid IAGP N RGD:5509061 20190808 MGI PMID:23024809 62335 Xdh xanthine dehydrogenase gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20240509 MGI PMID:31659168 62335 Xdh xanthine dehydrogenase gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:12502743 62335 Xdh xanthine dehydrogenase gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:15528468 62335 Xdh xanthine dehydrogenase gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:15528468 62335 Xdh xanthine dehydrogenase gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20190808 MGI PMID:23024809 62335 Xdh xanthine dehydrogenase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:15528468 62335 Xdh xanthine dehydrogenase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20190808 MGI PMID:23024809 62335 Xdh xanthine dehydrogenase gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:12502743 62335 Xdh xanthine dehydrogenase gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:12502743 62335 Xdh xanthine dehydrogenase gene MP:0008244 abnormal peritoneal macrophage morphology IAGP N RGD:5509061 20240509 MGI PMID:31659168 62335 Xdh xanthine dehydrogenase gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:15528468 62335 Xdh xanthine dehydrogenase gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20190808 MGI PMID:23024809 62335 Xdh xanthine dehydrogenase gene MP:0008806 increased circulating amylase level IAGP N RGD:5509061 20141003 MGI PMID:15528468 62335 Xdh xanthine dehydrogenase gene MP:0008822 decreased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:15528468 62335 Xdh xanthine dehydrogenase gene MP:0008822 decreased blood uric acid level IAGP N RGD:5509061 20190808 MGI PMID:23024809 62335 Xdh xanthine dehydrogenase gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20190808 MGI PMID:23024809 62335 Xdh xanthine dehydrogenase gene MP:0009645 crystalluria IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12502743 62335 Xdh xanthine dehydrogenase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15528468 62335 Xdh xanthine dehydrogenase gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0031479 increased urine xanthine level IAGP N RGD:5509061 20230810 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0031484 increased urine hypoxanthine level IAGP N RGD:5509061 20230810 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0031487 increased circulating hypoxanthine level IAGP N RGD:5509061 20230810 MGI PMID:19667249 62335 Xdh xanthine dehydrogenase gene MP:0031490 increased circulating xanthine level IAGP N RGD:5509061 20230810 MGI PMID:19667249 62336 Htr6 5-hydroxytryptamine (serotonin) receptor 6 gene MP:0001258 decreased body length IEA N RGD:5509061 20111116 MGI 62336 Htr6 5-hydroxytryptamine (serotonin) receptor 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18755168 62336 Htr6 5-hydroxytryptamine (serotonin) receptor 6 gene MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20141003 MGI PMID:16452990 62336 Htr6 5-hydroxytryptamine (serotonin) receptor 6 gene MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:16452990 62336 Htr6 5-hydroxytryptamine (serotonin) receptor 6 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18755168 62336 Htr6 5-hydroxytryptamine (serotonin) receptor 6 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:18755168 62336 Htr6 5-hydroxytryptamine (serotonin) receptor 6 gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20160421 MGI PMID:18755168 62337 Csnk1e casein kinase 1, epsilon gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20171012 MGI PMID:18400165 62337 Csnk1e casein kinase 1, epsilon gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:18400165 62337 Csnk1e casein kinase 1, epsilon gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:19414593 62337 Csnk1e casein kinase 1, epsilon gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:18400165 62338 Thbs4 thrombospondin 4 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:22362893 62338 Thbs4 thrombospondin 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22362893 62338 Thbs4 thrombospondin 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:22362893 62338 Thbs4 thrombospondin 4 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20240523 MGI PMID:26139464 62338 Thbs4 thrombospondin 4 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20240523 MGI PMID:26139464 62338 Thbs4 thrombospondin 4 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20240523 MGI PMID:26139464 62338 Thbs4 thrombospondin 4 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:22362893 62338 Thbs4 thrombospondin 4 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22362893 62338 Thbs4 thrombospondin 4 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20240523 MGI PMID:31974349 62338 Thbs4 thrombospondin 4 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:22362893 62338 Thbs4 thrombospondin 4 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20240523 MGI PMID:32686880 62338 Thbs4 thrombospondin 4 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:22362893 62338 Thbs4 thrombospondin 4 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20240523 MGI PMID:31974349 62338 Thbs4 thrombospondin 4 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20240523 MGI PMID:32686880 62338 Thbs4 thrombospondin 4 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22362893 62338 Thbs4 thrombospondin 4 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20240523 MGI PMID:32686880 62338 Thbs4 thrombospondin 4 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20240523 MGI PMID:32686880 62338 Thbs4 thrombospondin 4 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:22362893 62338 Thbs4 thrombospondin 4 gene MP:0014431 increased chemokine level IAGP N RGD:5509061 20240523 MGI PMID:32686880 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20151112 MGI PMID:21423341 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141016 MGI PMID:22705452 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141016 MGI PMID:22705452 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141016 MGI PMID:22705452 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141016 MGI PMID:22705452 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20151112 MGI PMID:21423341 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20151112 MGI PMID:21423341 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20151112 MGI PMID:21423341 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20151112 MGI PMID:21423341 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141016 MGI PMID:22705452 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0001893 non-obstructive hydrocephaly IAGP N RGD:5509061 20141016 MGI PMID:22705452 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141016 MGI PMID:22705452 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20151112 MGI PMID:21423341 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141016 MGI PMID:22705452 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141016 MGI PMID:22705452 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0003954 abnormal Reichert's membrane morphology IAGP N RGD:5509061 20151112 MGI PMID:21423341 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20151112 MGI PMID:21423341 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20151112 MGI PMID:21423341 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20151112 MGI PMID:21423341 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20141016 MGI PMID:22705452 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20141016 MGI PMID:22705452 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141016 MGI PMID:19843185 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20151112 MGI PMID:21423341 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20141016 MGI PMID:22705452 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0012065 increased astrocyte number IAGP N RGD:5509061 20141016 MGI PMID:22705452 62339 Ptbp1 polypyrimidine tract binding protein 1 gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20141016 MGI PMID:22705452 62340 Top2a topoisomerase (DNA) II alpha gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 62340 Top2a topoisomerase (DNA) II alpha gene MP:0000692 small spleen IEA N RGD:5509061 20220519 MGI 62340 Top2a topoisomerase (DNA) II alpha gene MP:0000706 small thymus IEA N RGD:5509061 20220519 MGI 62340 Top2a topoisomerase (DNA) II alpha gene MP:0001297 microphthalmia IEA N RGD:5509061 20220519 MGI 62340 Top2a topoisomerase (DNA) II alpha gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 62340 Top2a topoisomerase (DNA) II alpha gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 62340 Top2a topoisomerase (DNA) II alpha gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20231207 MGI 62340 Top2a topoisomerase (DNA) II alpha gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 62340 Top2a topoisomerase (DNA) II alpha gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200402 MGI 62340 Top2a topoisomerase (DNA) II alpha gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 62340 Top2a topoisomerase (DNA) II alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200402 MGI 62340 Top2a topoisomerase (DNA) II alpha gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 62340 Top2a topoisomerase (DNA) II alpha gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 62340 Top2a topoisomerase (DNA) II alpha gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0004343 small scapula IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0004355 short radius IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20201022 MGI 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170504 MGI 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20190117 MGI PMID:25340332 62342 Tnni2 troponin I, skeletal, fast 2 gene MP:0030439 decreased osteoblast proliferation IAGP N RGD:5509061 20190117 MGI PMID:25340332 62343 Pla2g5 phospholipase A2, group V gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:21169294 62343 Pla2g5 phospholipase A2, group V gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 62343 Pla2g5 phospholipase A2, group V gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 62343 Pla2g5 phospholipase A2, group V gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20240523 MGI 62343 Pla2g5 phospholipase A2, group V gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 62343 Pla2g5 phospholipase A2, group V gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 62343 Pla2g5 phospholipase A2, group V gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20240523 MGI 62343 Pla2g5 phospholipase A2, group V gene MP:0001147 small testis IEA N RGD:5509061 20240523 MGI 62343 Pla2g5 phospholipase A2, group V gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 62343 Pla2g5 phospholipase A2, group V gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:16407308 62343 Pla2g5 phospholipase A2, group V gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20240523 MGI 62343 Pla2g5 phospholipase A2, group V gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:14761945 62343 Pla2g5 phospholipase A2, group V gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 62343 Pla2g5 phospholipase A2, group V gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21169294 62343 Pla2g5 phospholipase A2, group V gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:21169294 62343 Pla2g5 phospholipase A2, group V gene MP:0003221 abnormal cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21169294 62343 Pla2g5 phospholipase A2, group V gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20240523 MGI 62343 Pla2g5 phospholipase A2, group V gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:21169294 62343 Pla2g5 phospholipase A2, group V gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20240523 MGI 62343 Pla2g5 phospholipase A2, group V gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:14761945 62343 Pla2g5 phospholipase A2, group V gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 62343 Pla2g5 phospholipase A2, group V gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20240523 MGI 62343 Pla2g5 phospholipase A2, group V gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21169294 62346 Pdyn prodynorphin gene MP:0001261 obese IAGP N RGD:5509061 20150129 MGI PMID:25157144 62346 Pdyn prodynorphin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12843270 62346 Pdyn prodynorphin gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12843270 62346 Pdyn prodynorphin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:11222667 62346 Pdyn prodynorphin gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:11717384 62346 Pdyn prodynorphin gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20141003 MGI PMID:11222667 62346 Pdyn prodynorphin gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:17347252 62346 Pdyn prodynorphin gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17347252 62346 Pdyn prodynorphin gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17347252 62346 Pdyn prodynorphin gene MP:0004152 abnormal circulating iron level IEA N RGD:5509061 20211021 MGI 62346 Pdyn prodynorphin gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0005316 abnormal response to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11222667 62346 Pdyn prodynorphin gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:11717384 62346 Pdyn prodynorphin gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:12843270 62346 Pdyn prodynorphin gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:17456788 62346 Pdyn prodynorphin gene MP:0011898 abnormal platelet cell number IEA N RGD:5509061 20211021 MGI 62347 Limk1 LIM domain kinase 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:12123613 62347 Limk1 LIM domain kinase 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:12123613 62347 Limk1 LIM domain kinase 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12123613 62347 Limk1 LIM domain kinase 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12123613 62347 Limk1 LIM domain kinase 1 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:12123613 62347 Limk1 LIM domain kinase 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:12123613 62347 Limk1 LIM domain kinase 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12123613 62347 Limk1 LIM domain kinase 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12123613 62347 Limk1 LIM domain kinase 1 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12123613 62347 Limk1 LIM domain kinase 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12123613 62347 Limk1 LIM domain kinase 1 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20190704 MGI PMID:12123613 62348 Limk2 LIM domain kinase 2 gene MP:0000088 short mandible IEA N RGD:5509061 20151112 MGI 62348 Limk2 LIM domain kinase 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:11784110 62348 Limk2 LIM domain kinase 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11784110 62348 Limk2 LIM domain kinase 2 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 62348 Limk2 LIM domain kinase 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:23071748 62348 Limk2 LIM domain kinase 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:23071748 62348 Limk2 LIM domain kinase 2 gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:23071748 62348 Limk2 LIM domain kinase 2 gene MP:0001314 cornea opacity IEA N RGD:5509061 20151112 MGI 62348 Limk2 LIM domain kinase 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11784110 62348 Limk2 LIM domain kinase 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:11784110 62348 Limk2 LIM domain kinase 2 gene MP:0003153 early eyelid opening IEA N RGD:5509061 20151112 MGI 62348 Limk2 LIM domain kinase 2 gene MP:0003313 abnormal locomotor activation IEA N RGD:5509061 20141003 MGI 62348 Limk2 LIM domain kinase 2 gene MP:0004357 long tibia IEA N RGD:5509061 20141003 MGI 62348 Limk2 LIM domain kinase 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:11784110 62348 Limk2 LIM domain kinase 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11784110 62348 Limk2 LIM domain kinase 2 gene MP:0005542 cornea vascularization IEA N RGD:5509061 20151112 MGI 62348 Limk2 LIM domain kinase 2 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23071748 62348 Limk2 LIM domain kinase 2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11784110 62348 Limk2 LIM domain kinase 2 gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:23071748 62348 Limk2 LIM domain kinase 2 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:23071748 62348 Limk2 LIM domain kinase 2 gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20141003 MGI PMID:23071748 62348 Limk2 LIM domain kinase 2 gene MP:0011481 anterior iris synechia IEA N RGD:5509061 20151112 MGI 62348 Limk2 LIM domain kinase 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:11784110 62348 Limk2 LIM domain kinase 2 gene MP:0030166 increased inner canthal distance IAGP N RGD:5509061 20171005 MGI PMID:26234751 62348 Limk2 LIM domain kinase 2 gene MP:0031212 decreased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:23071748 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000097 short maxilla IAGP N RGD:5509061 20151224 MGI PMID:25669657 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20111116 MGI 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0000755 hindlimb paralysis IEA N RGD:5509061 20111116 MGI 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0001265 decreased body size IEA N RGD:5509061 20170209 MGI 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0001300 ocular hypertelorism IEA N RGD:5509061 20170921 MGI 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0001349 excessive tearing IEA N RGD:5509061 20111116 MGI 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20170209 MGI 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0002233 abnormal nose morphology IEA N RGD:5509061 20170209 MGI 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20151224 MGI PMID:25669657 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20151224 MGI PMID:25669657 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:20530870 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0003416 premature bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0003416 premature bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:20530870 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0004053 abnormal synchondrosis IEA N RGD:5509061 20111116 MGI 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0010208 prognathia IAGP N RGD:5509061 20151224 MGI PMID:25669657 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0010714 iris coloboma IEA N RGD:5509061 20170209 MGI 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0010747 abnormal enamel organ morphology IAGP N RGD:5509061 20151224 MGI PMID:25669657 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0010941 abnormal foramen magnum morphology IAGP N RGD:5509061 20141003 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20170209 MGI 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0014166 ectopic cranial bone IAGP N RGD:5509061 20160407 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0030066 short face IEA N RGD:5509061 20170921 MGI 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0030104 round orbits IEA N RGD:5509061 20170928 MGI 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0030245 round head IAGP N RGD:5509061 20171102 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0030264 occipital bossing IAGP N RGD:5509061 20171026 MGI PMID:12379497 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0030420 short basicranium IAGP N RGD:5509061 20171214 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20180125 MGI PMID:11790802 62349 Ltbp3 latent transforming growth factor beta binding protein 3 gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20180125 MGI PMID:12379497 62350 Aoc3 amine oxidase, copper containing 3 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15664163 62350 Aoc3 amine oxidase, copper containing 3 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:15664163 62350 Aoc3 amine oxidase, copper containing 3 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:15664163 62350 Aoc3 amine oxidase, copper containing 3 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:15664163 62350 Aoc3 amine oxidase, copper containing 3 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:15664163 62351 Tesk1 testis specific protein kinase 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:10801981 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:14749383 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14749383 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0000433 microcephaly IAGP N RGD:5509061 20240919 MGI PMID:38566589 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20240919 MGI PMID:38566589 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:14749383 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0001258 decreased body length IAGP N RGD:5509061 20240919 MGI PMID:38566589 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240919 MGI PMID:38566589 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:14749383 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:14749383 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20240919 MGI PMID:38566589 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14749383 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14749383 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20240919 MGI PMID:38566589 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20240919 MGI PMID:38566589 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:14749383 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:14749383 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14749383 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0005352 small cranium IAGP N RGD:5509061 20240919 MGI PMID:38566589 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20240919 MGI PMID:38566589 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14749383 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14749383 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14749383 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20240919 MGI PMID:38566589 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14749383 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10801981 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14749383 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20240919 MGI PMID:38566589 62352 Ogt O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20240919 MGI PMID:38566589 62353 Insl6 insulin-like 6 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19520787 62353 Insl6 insulin-like 6 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19520787 62353 Insl6 insulin-like 6 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:19520787 62353 Insl6 insulin-like 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19520787 62353 Insl6 insulin-like 6 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19520787 62353 Insl6 insulin-like 6 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19520787 62353 Insl6 insulin-like 6 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19520787 62353 Insl6 insulin-like 6 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:19520787 62353 Insl6 insulin-like 6 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19520787 62353 Insl6 insulin-like 6 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19520787 62354 Mybbp1a MYB binding protein (P160) 1a gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 62354 Mybbp1a MYB binding protein (P160) 1a gene MP:0002608 increased hematocrit IEA N RGD:5509061 20211021 MGI 62354 Mybbp1a MYB binding protein (P160) 1a gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 62354 Mybbp1a MYB binding protein (P160) 1a gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 62354 Mybbp1a MYB binding protein (P160) 1a gene MP:0005505 thrombocytosis IEA N RGD:5509061 20201022 MGI 62354 Mybbp1a MYB binding protein (P160) 1a gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20211021 MGI 62354 Mybbp1a MYB binding protein (P160) 1a gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210520 MGI 62354 Mybbp1a MYB binding protein (P160) 1a gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:23056166 62354 Mybbp1a MYB binding protein (P160) 1a gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23056166 62354 Mybbp1a MYB binding protein (P160) 1a gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62354 Mybbp1a MYB binding protein (P160) 1a gene MP:0012129 failure of blastocyst formation IAGP N RGD:5509061 20141003 MGI PMID:23056166 62355 Zfp148 zinc finger protein 148 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 62355 Zfp148 zinc finger protein 148 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18250154 62355 Zfp148 zinc finger protein 148 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12524542 62355 Zfp148 zinc finger protein 148 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:23405202 62355 Zfp148 zinc finger protein 148 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 62355 Zfp148 zinc finger protein 148 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:23405202 62355 Zfp148 zinc finger protein 148 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 62355 Zfp148 zinc finger protein 148 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16517939 62355 Zfp148 zinc finger protein 148 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23405202 62355 Zfp148 zinc finger protein 148 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23395646 62355 Zfp148 zinc finger protein 148 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12524542 62355 Zfp148 zinc finger protein 148 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16517939 62355 Zfp148 zinc finger protein 148 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23405202 62355 Zfp148 zinc finger protein 148 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170105 MGI 62355 Zfp148 zinc finger protein 148 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18250154 62355 Zfp148 zinc finger protein 148 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12524542 62355 Zfp148 zinc finger protein 148 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23395646 62355 Zfp148 zinc finger protein 148 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18250154 62355 Zfp148 zinc finger protein 148 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:18250154 62355 Zfp148 zinc finger protein 148 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:23405202 62355 Zfp148 zinc finger protein 148 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18250154 62355 Zfp148 zinc finger protein 148 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12524542 62355 Zfp148 zinc finger protein 148 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:23405202 62355 Zfp148 zinc finger protein 148 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:16517939 62355 Zfp148 zinc finger protein 148 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16517939 62355 Zfp148 zinc finger protein 148 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23395646 62355 Zfp148 zinc finger protein 148 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:23395646 62355 Zfp148 zinc finger protein 148 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:23395646 62355 Zfp148 zinc finger protein 148 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:23405202 62355 Zfp148 zinc finger protein 148 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16517939 62355 Zfp148 zinc finger protein 148 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23405202 62355 Zfp148 zinc finger protein 148 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18250154 62355 Zfp148 zinc finger protein 148 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62355 Zfp148 zinc finger protein 148 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20170105 MGI 62356 Adra1d adrenergic receptor, alpha 1d gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15196805 62356 Adra1d adrenergic receptor, alpha 1d gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11901185 62356 Adra1d adrenergic receptor, alpha 1d gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:11901185 62356 Adra1d adrenergic receptor, alpha 1d gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12874602 62356 Adra1d adrenergic receptor, alpha 1d gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11901185 62356 Adra1d adrenergic receptor, alpha 1d gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:15196805 62356 Adra1d adrenergic receptor, alpha 1d gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:12874602 62356 Adra1d adrenergic receptor, alpha 1d gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:15196805 62356 Adra1d adrenergic receptor, alpha 1d gene MP:0004142 abnormal muscle tone IAGP N RGD:5509061 20141003 MGI PMID:15196805 62356 Adra1d adrenergic receptor, alpha 1d gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11901185 62356 Adra1d adrenergic receptor, alpha 1d gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:15196805 62356 Adra1d adrenergic receptor, alpha 1d gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:12874602 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19336225 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0000599 enlarged liver IEA N RGD:5509061 20210128 MGI 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0001158 abnormal prostate gland morphology IEA N RGD:5509061 20210826 MGI 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19336225 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19336225 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:19336225 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19336225 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:19336225 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19336225 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19336225 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62357 Extl3 exostosin-like glycosyltransferase 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0005046 absent spleen white pulp IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20200130 MGI PMID:12925567 62358 Slc37a4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 gene MP:0031003 increased kidney glycogen level IAGP N RGD:5509061 20200130 MGI PMID:12925567 62359 Mrpl23 mitochondrial ribosomal protein L23 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 62359 Mrpl23 mitochondrial ribosomal protein L23 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 62359 Mrpl23 mitochondrial ribosomal protein L23 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62360 Ptpro protein tyrosine phosphatase receptor type O gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11086029 62360 Ptpro protein tyrosine phosphatase receptor type O gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 62360 Ptpro protein tyrosine phosphatase receptor type O gene MP:0002906 increased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20111116 MGI 62360 Ptpro protein tyrosine phosphatase receptor type O gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11086029 62360 Ptpro protein tyrosine phosphatase receptor type O gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11086029 62360 Ptpro protein tyrosine phosphatase receptor type O gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:11086029 62360 Ptpro protein tyrosine phosphatase receptor type O gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:11086029 62361 Rpl29 ribosomal protein L29 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17195189 62361 Rpl29 ribosomal protein L29 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17195189 62361 Rpl29 ribosomal protein L29 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17195189 62361 Rpl29 ribosomal protein L29 gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:17195189 62361 Rpl29 ribosomal protein L29 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:17195189 62361 Rpl29 ribosomal protein L29 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17195189 62361 Rpl29 ribosomal protein L29 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17195189 62361 Rpl29 ribosomal protein L29 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:17195189 62362 Crabp2 cellular retinoic acid binding protein II gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 62362 Crabp2 cellular retinoic acid binding protein II gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 62362 Crabp2 cellular retinoic acid binding protein II gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:7768191 62362 Crabp2 cellular retinoic acid binding protein II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7768191 62362 Crabp2 cellular retinoic acid binding protein II gene MP:0002833 increased heart weight IEA N RGD:5509061 20201022 MGI 62362 Crabp2 cellular retinoic acid binding protein II gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 62362 Crabp2 cellular retinoic acid binding protein II gene MP:0009744 postaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:7720575 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19635813 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19635813 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:19635813 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:19635813 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:16950158 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21423695 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16950158 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:16950158 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19635813 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:21423695 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:18394802 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20141003 MGI PMID:16950158 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:19635813 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:16950158 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:19635813 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:21423695 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0004836 abnormal synaptic acetylcholine release IAGP N RGD:5509061 20141003 MGI PMID:16950158 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0004836 abnormal synaptic acetylcholine release IAGP N RGD:5509061 20141003 MGI PMID:19635813 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19635813 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:19635813 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:19635813 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16950158 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19635813 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:16950158 62364 Slc18a3 solute carrier family 18 (vesicular monoamine), member 3 gene MP:0030676 increased acetylcholine level IAGP N RGD:5509061 20180927 MGI PMID:19635813 62365 P2rx4 purinergic receptor P2X, ligand-gated ion channel 4 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:16327800 62365 P2rx4 purinergic receptor P2X, ligand-gated ion channel 4 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16943557 62365 P2rx4 purinergic receptor P2X, ligand-gated ion channel 4 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:16327800 62365 P2rx4 purinergic receptor P2X, ligand-gated ion channel 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17825926 62365 P2rx4 purinergic receptor P2X, ligand-gated ion channel 4 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20240523 MGI PMID:34548395 62365 P2rx4 purinergic receptor P2X, ligand-gated ion channel 4 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 62365 P2rx4 purinergic receptor P2X, ligand-gated ion channel 4 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16327800 62365 P2rx4 purinergic receptor P2X, ligand-gated ion channel 4 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16327800 62365 P2rx4 purinergic receptor P2X, ligand-gated ion channel 4 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16327800 62365 P2rx4 purinergic receptor P2X, ligand-gated ion channel 4 gene MP:0005298 abnormal clavicle morphology IEA N RGD:5509061 20160421 MGI 62365 P2rx4 purinergic receptor P2X, ligand-gated ion channel 4 gene MP:0011742 decreased urine nitrite level IAGP N RGD:5509061 20141003 MGI PMID:16327800 62365 P2rx4 purinergic receptor P2X, ligand-gated ion channel 4 gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16327800 62365 P2rx4 purinergic receptor P2X, ligand-gated ion channel 4 gene MP:0013296 abnormal susceptibility to induced colitis IAGP N RGD:5509061 20240523 MGI PMID:34548395 62366 Inhba inhibin beta-A gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:7885473 62366 Inhba inhibin beta-A gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0000424 retarded hair growth IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17609433 62366 Inhba inhibin beta-A gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20810712 62366 Inhba inhibin beta-A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:7885473 62366 Inhba inhibin beta-A gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:7885473 62366 Inhba inhibin beta-A gene MP:0001435 absent suckling reflex IAGP N RGD:5509061 20141003 MGI PMID:7885473 62366 Inhba inhibin beta-A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17609433 62366 Inhba inhibin beta-A gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17609433 62366 Inhba inhibin beta-A gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17609433 62366 Inhba inhibin beta-A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17609433 62366 Inhba inhibin beta-A gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:17592132 62366 Inhba inhibin beta-A gene MP:0002681 increased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:17609433 62366 Inhba inhibin beta-A gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0003346 abnormal pectoral muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:20810712 62366 Inhba inhibin beta-A gene MP:0003529 enlarged clitoris IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0003599 large penis IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:17592132 62366 Inhba inhibin beta-A gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20141003 MGI PMID:7885473 62366 Inhba inhibin beta-A gene MP:0004791 absent lower incisors IAGP N RGD:5509061 20141003 MGI PMID:7885473 62366 Inhba inhibin beta-A gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:17609433 62366 Inhba inhibin beta-A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0004855 increased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:17609433 62366 Inhba inhibin beta-A gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17592132 62366 Inhba inhibin beta-A gene MP:0005131 increased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17609433 62366 Inhba inhibin beta-A gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0006198 enophthalmos IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0008975 delayed male fertility IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0009200 enlarged external male genitalia IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17609433 62366 Inhba inhibin beta-A gene MP:0009421 increased gastrocnemius weight IAGP N RGD:5509061 20141003 MGI PMID:20810712 62366 Inhba inhibin beta-A gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20141003 MGI PMID:17609433 62366 Inhba inhibin beta-A gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20220407 MGI PMID:17609433 62366 Inhba inhibin beta-A gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:7885473 62366 Inhba inhibin beta-A gene MP:0009894 absent hard palate IAGP N RGD:5509061 20141003 MGI PMID:7885473 62366 Inhba inhibin beta-A gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:10932194 62366 Inhba inhibin beta-A gene MP:0010226 increased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:20810712 62366 Inhba inhibin beta-A gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:7885473 62366 Inhba inhibin beta-A gene MP:0010238 increased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:20810712 62366 Inhba inhibin beta-A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17609433 62366 Inhba inhibin beta-A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7885473 62366 Inhba inhibin beta-A gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7885473 62366 Inhba inhibin beta-A gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10932194 62367 Rpn2 ribophorin II gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20160804 MGI 62367 Rpn2 ribophorin II gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20160804 MGI 62367 Rpn2 ribophorin II gene MP:0003443 increased circulating glycerol level IEA N RGD:5509061 20160804 MGI 62367 Rpn2 ribophorin II gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62368 Ptges prostaglandin E synthase gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23204105 62368 Ptges prostaglandin E synthase gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23624557 62368 Ptges prostaglandin E synthase gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15140897 62368 Ptges prostaglandin E synthase gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12835414 62368 Ptges prostaglandin E synthase gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:14566340 62368 Ptges prostaglandin E synthase gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:14566340 62368 Ptges prostaglandin E synthase gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23204105 62368 Ptges prostaglandin E synthase gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:15140897 62368 Ptges prostaglandin E synthase gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15140897 62368 Ptges prostaglandin E synthase gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:23204105 62368 Ptges prostaglandin E synthase gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23624557 62368 Ptges prostaglandin E synthase gene MP:0009811 abnormal prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:15140897 62368 Ptges prostaglandin E synthase gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:23204105 62368 Ptges prostaglandin E synthase gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:16204198 62368 Ptges prostaglandin E synthase gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:23204105 62368 Ptges prostaglandin E synthase gene MP:0009817 decreased leukotriene level IAGP N RGD:5509061 20141003 MGI PMID:12023384 62369 Sebox SEBOX homeobox gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 62371 Gosr2 golgi SNAP receptor complex member 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 62371 Gosr2 golgi SNAP receptor complex member 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 62371 Gosr2 golgi SNAP receptor complex member 2 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 62371 Gosr2 golgi SNAP receptor complex member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 62372 Cd63 CD63 antigen gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:19075008 62372 Cd63 CD63 antigen gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:19075008 62372 Cd63 CD63 antigen gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:19075008 62372 Cd63 CD63 antigen gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:19075008 62372 Cd63 CD63 antigen gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19075008 62372 Cd63 CD63 antigen gene MP:0011757 abnormal kidney collecting duct principal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19075008 62372 Cd63 CD63 antigen gene MP:0014483 increased feces water content IAGP N RGD:5509061 20240704 MGI PMID:19075008 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:11425898 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:8543157 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:10615124 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10615124 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17426285 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:18579678 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11500373 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:11500373 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:15496443 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:8543157 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11500373 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:8543157 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:8543157 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0001062 absent oculomotor nerve IAGP N RGD:5509061 20141003 MGI PMID:11500373 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0001064 absent trochlear nerve IAGP N RGD:5509061 20141003 MGI PMID:11500373 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:10952889 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:10205173 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10205173 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11500373 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21093323 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:8543157 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:10615124 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:14702043 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21093323 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10804175 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11500373 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:8543157 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:18579678 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21205788 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11023859 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002653 abnormal ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002659 pituitary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17426285 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:10615124 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:22146645 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:19619492 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:14702043 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:19619492 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11500373 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0003250 absent gallbladder IAGP N RGD:5509061 20141003 MGI PMID:14702043 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:8543157 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:11500373 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:15496443 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:10952889 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0003647 absent oligodendrocytes IAGP N RGD:5509061 20141003 MGI PMID:15496443 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11500373 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141003 MGI PMID:17426285 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0003817 abnormal pituitary diverticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:17426285 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:10615124 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:19619492 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:21205788 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:22529374 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11500373 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0004164 abnormal neurohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:17426285 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18579678 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0004280 abnormal oculomotor nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11500373 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0004327 increased vestibular hair cell number IAGP N RGD:5509061 20141003 MGI PMID:11023859 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0004327 increased vestibular hair cell number IAGP N RGD:5509061 20141003 MGI PMID:11425898 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:11023859 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:11425898 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:11023859 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:11425898 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21093323 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24179156 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:21093323 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:10615124 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0005603 neuron hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10205173 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10205173 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:11425898 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11425898 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0006292 abnormal nasal placode morphology IAGP N RGD:5509061 20141003 MGI PMID:10804175 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0006294 absent optic vesicle IAGP N RGD:5509061 20141003 MGI PMID:15496443 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21093323 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0008328 increased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:17426285 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21093323 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0008367 absent pituitary intermediate lobe IAGP N RGD:5509061 20141003 MGI PMID:17426285 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:18579678 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0008949 increased Cajal-Retzius cell number IAGP N RGD:5509061 20141003 MGI PMID:18579678 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0009159 increased pancreatic acinar cell number IAGP N RGD:5509061 20141003 MGI PMID:22146645 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22529374 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0009463 abnormal pituitary infundibular stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:17426285 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0009493 abnormal cystic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:14702043 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0009495 abnormal common bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:19619492 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0009498 abnormal extrahepatic bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:19619492 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18579678 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:8543157 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0010129 increased DN1 thymic pro-T cell number IAGP N RGD:5509061 20141003 MGI PMID:21093323 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0010130 decreased DN1 thymic pro-T cell number IAGP N RGD:5509061 20141003 MGI PMID:21093323 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0010132 decreased DN2 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21093323 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0010134 decreased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21093323 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21093323 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0010171 abnormal centroacinar cell of Langerhans morphology IAGP N RGD:5509061 20141003 MGI PMID:22146645 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21093323 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0010915 increased solitary pulmonary neuroendocrine cell number IAGP N RGD:5509061 20141003 MGI PMID:10952889 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0010919 increased number of pulmonary neuroendocrine bodies IAGP N RGD:5509061 20141003 MGI PMID:10952889 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0010949 decreased club cell number IAGP N RGD:5509061 20141003 MGI PMID:10952889 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8543157 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21205788 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11500373 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15496443 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8543157 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8543157 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:11500373 62373 Hes1 hes family bHLH transcription factor 1 gene MP:0012686 everted embryonic neuroepithelium IAGP N RGD:5509061 20141003 MGI PMID:8543157 62375 Kcna6 potassium voltage-gated channel, shaker-related, subfamily, member 6 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20240523 MGI 62375 Kcna6 potassium voltage-gated channel, shaker-related, subfamily, member 6 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20111116 MGI 62375 Kcna6 potassium voltage-gated channel, shaker-related, subfamily, member 6 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 62375 Kcna6 potassium voltage-gated channel, shaker-related, subfamily, member 6 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 62376 Cblif cobalamin binding intrinsic factor gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0003718 maternal effect IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0005015 increased T cell number IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0010330 abnormal circulating lipoprotein level IAGP N RGD:5509061 20170622 MGI PMID:27329747 62376 Cblif cobalamin binding intrinsic factor gene MP:0011227 abnormal vitamin B12 level IAGP N RGD:5509061 20170622 MGI PMID:27329747 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0000774 decreased brain size IEA N RGD:5509061 20210826 MGI 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150430 MGI PMID:20956558 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150430 MGI PMID:20956558 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210826 MGI 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001304 cataract IEA N RGD:5509061 20220519 MGI 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20230601 MGI 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220811 MGI 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001785 edema IEA N RGD:5509061 20230601 MGI 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001925 male infertility IEA N RGD:5509061 20220519 MGI 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210826 MGI 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0005162 carpoptosis IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20150430 MGI PMID:20956558 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20150430 MGI PMID:20956558 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19805361 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20150430 MGI PMID:20956558 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 62379 Mapk6 mitogen-activated protein kinase 6 gene MP:0020863 abnormal suckling reflex IAGP N RGD:5509061 20220922 MGI PMID:19805361 62380 P2ry2 purinergic receptor P2Y, G-protein coupled 2 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10473605 62380 P2ry2 purinergic receptor P2Y, G-protein coupled 2 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10473606 62380 P2ry2 purinergic receptor P2Y, G-protein coupled 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:10473605 62380 P2ry2 purinergic receptor P2Y, G-protein coupled 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:10473606 62380 P2ry2 purinergic receptor P2Y, G-protein coupled 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:16365320 62380 P2ry2 purinergic receptor P2Y, G-protein coupled 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:16365320 62380 P2ry2 purinergic receptor P2Y, G-protein coupled 2 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20161027 MGI PMID:26168216 62380 P2ry2 purinergic receptor P2Y, G-protein coupled 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16365320 62380 P2ry2 purinergic receptor P2Y, G-protein coupled 2 gene MP:0012045 increased susceptibility to hypertension IAGP N RGD:5509061 20161027 MGI PMID:26168216 62393 Htr5b 5-hydroxytryptamine (serotonin) receptor 5B gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:15713641 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:15930105 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20190725 MGI PMID:28467426 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:15930105 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15930105 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:21159799 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:16923958 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16923958 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16923958 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16923958 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19289493 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20141003 MGI PMID:21159799 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17442925 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17442925 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17210696 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16923958 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17442925 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:15930105 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:16923958 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:21159799 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0002194 maximal tonic hindlimb extension seizures IAGP N RGD:5509061 20141003 MGI PMID:21159799 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:21159799 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:21159799 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:16923958 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21906027 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21159799 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:21159799 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:21159799 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16923958 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442925 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442925 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:21159799 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16923958 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19289493 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:16923958 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17442925 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:15930105 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0008282 enlarged hippocampus IAGP N RGD:5509061 20141003 MGI PMID:21159799 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20190725 MGI PMID:28467426 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21906027 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16923958 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0012296 impaired discrimination learning IAGP N RGD:5509061 20190725 MGI PMID:28467426 62395 Akt3 thymoma viral proto-oncogene 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:28467426 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19801575 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19801575 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141106 MGI PMID:24662293 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180809 MGI PMID:22689911 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20160825 MGI PMID:24194321 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:16716308 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141106 MGI PMID:24662293 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16716308 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20160804 MGI PMID:25132496 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141106 MGI PMID:24662293 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141106 MGI PMID:24662293 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:9531536 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141106 MGI PMID:24662293 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141106 MGI PMID:24662293 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20160804 MGI PMID:25872946 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141106 MGI PMID:24662293 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11526215 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9531536 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20190307 MGI PMID:30188326 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141106 MGI PMID:24662293 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20180809 MGI PMID:22689911 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141106 MGI PMID:24662293 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20141003 MGI PMID:19752026 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0011081 decreased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19752026 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20180809 MGI PMID:22689911 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0011968 decreased threshold for auditory brainstem response IAGP N RGD:5509061 20190307 MGI PMID:30188326 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20180809 MGI PMID:22689911 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:9531536 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0020935 decreased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16936275 62396 Ddit3 DNA-damage inducible transcript 3 gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240321 MGI PMID:24662293 68442 Gabre gamma-aminobutyric acid (GABA) A receptor, subunit epsilon gene MP:0001921 reduced fertility IAGP N RGD:5509061 20191031 MGI PMID:29115488 68442 Gabre gamma-aminobutyric acid (GABA) A receptor, subunit epsilon gene MP:0009778 impaired behavioral response to anesthetic IAGP N RGD:5509061 20191031 MGI PMID:29115488 68442 Gabre gamma-aminobutyric acid (GABA) A receptor, subunit epsilon gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0003046 liver cirrhosis IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0005218 abnormal pancreatic delta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0009180 increased pancreatic delta cell number IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19934005 68443 Sec61a1 SEC61 translocon subunit alpha 1 gene MP:0014117 increased pancreatic beta cell apoptosis IAGP N RGD:5509061 20160324 MGI PMID:19934005 68447 Rab2a RAB2A, member RAS oncogene family gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200402 MGI 68447 Rab2a RAB2A, member RAS oncogene family gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 68447 Rab2a RAB2A, member RAS oncogene family gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20221215 MGI 68447 Rab2a RAB2A, member RAS oncogene family gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20221215 MGI 68447 Rab2a RAB2A, member RAS oncogene family gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 68447 Rab2a RAB2A, member RAS oncogene family gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 68447 Rab2a RAB2A, member RAS oncogene family gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20221215 MGI 68447 Rab2a RAB2A, member RAS oncogene family gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 68449 Pdlim1 PDZ and LIM domain 1 (elfin) gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:22955732 68449 Pdlim1 PDZ and LIM domain 1 (elfin) gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:22955732 68449 Pdlim1 PDZ and LIM domain 1 (elfin) gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:22955732 68449 Pdlim1 PDZ and LIM domain 1 (elfin) gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20141003 MGI PMID:22955732 68449 Pdlim1 PDZ and LIM domain 1 (elfin) gene MP:0009586 increased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:22955732 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:16174646 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:7749225 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:7749225 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:16174646 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20220804 MGI PMID:34726235 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:15269181 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:7749225 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:9883726 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:15269181 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20220804 MGI PMID:34726235 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20230720 MGI PMID:36413117 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15269181 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220804 MGI PMID:34726235 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230720 MGI PMID:36413117 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16174646 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220804 MGI PMID:34726235 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20230720 MGI PMID:36413117 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:7749225 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20220804 MGI PMID:34726235 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:7749225 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:7749225 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20230720 MGI PMID:36413117 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20220804 MGI PMID:34726235 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001957 apnea IAGP N RGD:5509061 20220804 MGI PMID:34726235 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20230720 MGI PMID:36413117 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16174646 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7749225 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9883726 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:9883726 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20220804 MGI PMID:34726235 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20230720 MGI PMID:36413117 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:15269181 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20220804 MGI PMID:34726235 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:16174646 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:16174646 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210826 MGI 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:7749225 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0003158 dysphagia IAGP N RGD:5509061 20141003 MGI PMID:16174646 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0003177 allodynia IAGP N RGD:5509061 20230720 MGI PMID:36413117 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20230720 MGI PMID:36413117 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0003898 abnormal QRS complex IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0003901 abnormal PR interval IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0003928 increased heart rate variability IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0004235 abnormal masseter muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:7749225 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0004239 abnormal temporalis muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:7749225 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0004545 enlarged esophagus IAGP N RGD:5509061 20141003 MGI PMID:16174646 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20230720 MGI PMID:36413117 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:15269181 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:16174646 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20220804 MGI PMID:34726235 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0005576 decreased pulmonary ventilation IAGP N RGD:5509061 20220804 MGI PMID:34726235 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0005585 increased tidal volume IAGP N RGD:5509061 20220804 MGI PMID:34726235 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20230720 MGI PMID:36413117 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20220804 MGI PMID:34726235 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20230720 MGI PMID:36413117 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0009434 paraparesis IAGP N RGD:5509061 20230720 MGI PMID:36413117 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20230720 MGI PMID:36413117 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200402 MGI 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20230720 MGI PMID:36413117 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0010334 pleural effusion IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:15069027 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20220804 MGI PMID:34726235 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200402 MGI 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0013138 thin body IAGP N RGD:5509061 20230720 MGI PMID:36413117 68451 Ighmbp2 immunoglobulin mu DNA binding protein 2 gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20161013 MGI PMID:15269181 68453 Vapb vesicle-associated membrane protein, associated protein B and C gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23446633 68453 Vapb vesicle-associated membrane protein, associated protein B and C gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20151217 MGI PMID:26362257 68453 Vapb vesicle-associated membrane protein, associated protein B and C gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23446633 68453 Vapb vesicle-associated membrane protein, associated protein B and C gene MP:0001405 impaired coordination IAGP N RGD:5509061 20151217 MGI PMID:26362257 68453 Vapb vesicle-associated membrane protein, associated protein B and C gene MP:0003858 enhanced coordination IEA N RGD:5509061 20141003 MGI 68453 Vapb vesicle-associated membrane protein, associated protein B and C gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:23446633 68453 Vapb vesicle-associated membrane protein, associated protein B and C gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20220811 MGI 68453 Vapb vesicle-associated membrane protein, associated protein B and C gene MP:0005405 axon degeneration IAGP N RGD:5509061 20151217 MGI PMID:26362257 68453 Vapb vesicle-associated membrane protein, associated protein B and C gene MP:0005655 increased aggression IEA N RGD:5509061 20210128 MGI 68453 Vapb vesicle-associated membrane protein, associated protein B and C gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20151217 MGI PMID:26362257 68453 Vapb vesicle-associated membrane protein, associated protein B and C gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20151217 MGI PMID:26362257 68453 Vapb vesicle-associated membrane protein, associated protein B and C gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20151217 MGI PMID:26362257 68453 Vapb vesicle-associated membrane protein, associated protein B and C gene MP:0011975 neuronal cytoplasmic inclusions IAGP N RGD:5509061 20151217 MGI PMID:26362257 68455 Hap1 huntingtin-associated protein 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:11971876 68455 Hap1 huntingtin-associated protein 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11971876 68455 Hap1 huntingtin-associated protein 1 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:12890790 68455 Hap1 huntingtin-associated protein 1 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:20304926 68455 Hap1 huntingtin-associated protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11971876 68455 Hap1 huntingtin-associated protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20304926 68455 Hap1 huntingtin-associated protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151126 MGI PMID:25875952 68455 Hap1 huntingtin-associated protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11971876 68455 Hap1 huntingtin-associated protein 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20304926 68455 Hap1 huntingtin-associated protein 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20151112 MGI PMID:25875952 68455 Hap1 huntingtin-associated protein 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:11971876 68455 Hap1 huntingtin-associated protein 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:11971876 68455 Hap1 huntingtin-associated protein 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:15496430 68455 Hap1 huntingtin-associated protein 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20151126 MGI PMID:25875952 68455 Hap1 huntingtin-associated protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15496430 68455 Hap1 huntingtin-associated protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15496430 68455 Hap1 huntingtin-associated protein 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:11971876 68455 Hap1 huntingtin-associated protein 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:12890790 68455 Hap1 huntingtin-associated protein 1 gene MP:0003064 decreased coping response IAGP N RGD:5509061 20151112 MGI PMID:25875952 68455 Hap1 huntingtin-associated protein 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11971876 68455 Hap1 huntingtin-associated protein 1 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:11971876 68455 Hap1 huntingtin-associated protein 1 gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:11971876 68455 Hap1 huntingtin-associated protein 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20240523 MGI 68455 Hap1 huntingtin-associated protein 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11971876 68455 Hap1 huntingtin-associated protein 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:11971876 68455 Hap1 huntingtin-associated protein 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:15496430 68455 Hap1 huntingtin-associated protein 1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:20304926 68455 Hap1 huntingtin-associated protein 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11971876 68455 Hap1 huntingtin-associated protein 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:12890790 68455 Hap1 huntingtin-associated protein 1 gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20141003 MGI PMID:24366265 68455 Hap1 huntingtin-associated protein 1 gene MP:0008845 abnormal paraventricular hypothalamic nucleus morphology IAGP N RGD:5509061 20180315 MGI PMID:12890790 68455 Hap1 huntingtin-associated protein 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:11971876 68455 Hap1 huntingtin-associated protein 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:12890790 68455 Hap1 huntingtin-associated protein 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:15496430 68455 Hap1 huntingtin-associated protein 1 gene MP:0009710 anhedonia IAGP N RGD:5509061 20151126 MGI PMID:25875952 68455 Hap1 huntingtin-associated protein 1 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20151112 MGI PMID:25875952 68455 Hap1 huntingtin-associated protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11971876 68455 Hap1 huntingtin-associated protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12890790 68455 Hap1 huntingtin-associated protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15496430 68455 Hap1 huntingtin-associated protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15496430 68455 Hap1 huntingtin-associated protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 68455 Hap1 huntingtin-associated protein 1 gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20151112 MGI PMID:25875952 68455 Hap1 huntingtin-associated protein 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:20304926 68455 Hap1 huntingtin-associated protein 1 gene MP:0012165 absent neural folds IAGP N RGD:5509061 20141003 MGI PMID:15496430 68455 Hap1 huntingtin-associated protein 1 gene MP:0020556 abnormal ventromedial hypothalamic nucleus morphology IAGP N RGD:5509061 20180315 MGI PMID:12890790 68457 Slc2a5 solute carrier family 2 (facilitated glucose transporter), member 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 68457 Slc2a5 solute carrier family 2 (facilitated glucose transporter), member 5 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 68457 Slc2a5 solute carrier family 2 (facilitated glucose transporter), member 5 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210520 MGI 68457 Slc2a5 solute carrier family 2 (facilitated glucose transporter), member 5 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 68457 Slc2a5 solute carrier family 2 (facilitated glucose transporter), member 5 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 68457 Slc2a5 solute carrier family 2 (facilitated glucose transporter), member 5 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 68457 Slc2a5 solute carrier family 2 (facilitated glucose transporter), member 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 68457 Slc2a5 solute carrier family 2 (facilitated glucose transporter), member 5 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20201022 MGI 68457 Slc2a5 solute carrier family 2 (facilitated glucose transporter), member 5 gene MP:0009709 hydrometra IEA N RGD:5509061 20201022 MGI 68459 Pde1a phosphodiesterase 1A, calmodulin-dependent gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20210603 MGI PMID:28750036 68459 Pde1a phosphodiesterase 1A, calmodulin-dependent gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 68459 Pde1a phosphodiesterase 1A, calmodulin-dependent gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 68459 Pde1a phosphodiesterase 1A, calmodulin-dependent gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20210603 MGI PMID:28750036 68459 Pde1a phosphodiesterase 1A, calmodulin-dependent gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20240523 MGI 68459 Pde1a phosphodiesterase 1A, calmodulin-dependent gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20210603 MGI PMID:28750036 68459 Pde1a phosphodiesterase 1A, calmodulin-dependent gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20210603 MGI PMID:28750036 68459 Pde1a phosphodiesterase 1A, calmodulin-dependent gene MP:0003675 kidney cyst IAGP N RGD:5509061 20210603 MGI PMID:28750036 68459 Pde1a phosphodiesterase 1A, calmodulin-dependent gene MP:0003960 increased lean body mass IEA N RGD:5509061 20221215 MGI 68459 Pde1a phosphodiesterase 1A, calmodulin-dependent gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20200402 MGI 68459 Pde1a phosphodiesterase 1A, calmodulin-dependent gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20210603 MGI PMID:28750036 68459 Pde1a phosphodiesterase 1A, calmodulin-dependent gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20221215 MGI 68459 Pde1a phosphodiesterase 1A, calmodulin-dependent gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20210603 MGI PMID:28750036 68459 Pde1a phosphodiesterase 1A, calmodulin-dependent gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20210603 MGI PMID:28750036 68459 Pde1a phosphodiesterase 1A, calmodulin-dependent gene MP:0031635 increased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:28750036 68461 Thop1 thimet oligopeptidase 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20201231 MGI PMID:31431000 68461 Thop1 thimet oligopeptidase 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20231207 MGI 68461 Thop1 thimet oligopeptidase 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20201231 MGI PMID:31431000 68461 Thop1 thimet oligopeptidase 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20231207 MGI 68461 Thop1 thimet oligopeptidase 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20231207 MGI 68461 Thop1 thimet oligopeptidase 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20231207 MGI 68461 Thop1 thimet oligopeptidase 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 68461 Thop1 thimet oligopeptidase 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 68461 Thop1 thimet oligopeptidase 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 68461 Thop1 thimet oligopeptidase 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 68461 Thop1 thimet oligopeptidase 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 68461 Thop1 thimet oligopeptidase 1 gene MP:0002409 decreased susceptibility to infection IAGP N RGD:5509061 20201231 MGI PMID:31431000 68461 Thop1 thimet oligopeptidase 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20231207 MGI 68461 Thop1 thimet oligopeptidase 1 gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 68461 Thop1 thimet oligopeptidase 1 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20231207 MGI 68461 Thop1 thimet oligopeptidase 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20201231 MGI PMID:31431000 68461 Thop1 thimet oligopeptidase 1 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20201231 MGI PMID:31431000 68461 Thop1 thimet oligopeptidase 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20201231 MGI PMID:31431000 68461 Thop1 thimet oligopeptidase 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20201231 MGI PMID:31431000 68461 Thop1 thimet oligopeptidase 1 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20201231 MGI PMID:31431000 68461 Thop1 thimet oligopeptidase 1 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20201231 MGI PMID:31431000 68461 Thop1 thimet oligopeptidase 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20201231 MGI PMID:31431000 68461 Thop1 thimet oligopeptidase 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20201231 MGI PMID:31431000 68461 Thop1 thimet oligopeptidase 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20201231 MGI PMID:31431000 68461 Thop1 thimet oligopeptidase 1 gene MP:0009786 decreased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20201231 MGI PMID:31431000 68462 Gabrq gamma-aminobutyric acid type A receptor subunit theta gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20111116 MGI 68464 Pde1c phosphodiesterase 1C gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:19305400 68464 Pde1c phosphodiesterase 1C gene MP:0009562 abnormal odor adaptation IAGP N RGD:5509061 20141003 MGI PMID:19305400 68464 Pde1c phosphodiesterase 1C gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 68466 Gpr12 G-protein coupled receptor 12 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16887097 68466 Gpr12 G-protein coupled receptor 12 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16887097 68466 Gpr12 G-protein coupled receptor 12 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:16887097 68466 Gpr12 G-protein coupled receptor 12 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16887097 68466 Gpr12 G-protein coupled receptor 12 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16887097 68466 Gpr12 G-protein coupled receptor 12 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16887097 68466 Gpr12 G-protein coupled receptor 12 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16887097 68466 Gpr12 G-protein coupled receptor 12 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:16887097 68466 Gpr12 G-protein coupled receptor 12 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:16887097 68466 Gpr12 G-protein coupled receptor 12 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16887097 68466 Gpr12 G-protein coupled receptor 12 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16887097 68466 Gpr12 G-protein coupled receptor 12 gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16887097 68466 Gpr12 G-protein coupled receptor 12 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16887097 68466 Gpr12 G-protein coupled receptor 12 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:16887097 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20190228 MGI PMID:27383011 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15138255 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:12006579 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:15138255 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15138255 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15138255 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12006579 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0001967 deafness IAGP N RGD:5509061 20170420 MGI PMID:26805784 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20170420 MGI PMID:19903857 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11553273 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:20068174 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141218 MGI PMID:24913235 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11553273 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11553273 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:21642988 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20170420 MGI PMID:19903857 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:11553273 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0003143 enlarged otoliths IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0003144 decreased otolith number IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0003144 decreased otolith number IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0003144 decreased otolith number IAGP N RGD:5509061 20170420 MGI PMID:26805784 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:20068174 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20068174 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:11553273 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004305 abnormal Rosenthal canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004329 vestibular saccular degeneration IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004331 vestibular saccular macula degeneration IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004334 utricular macular degeneration IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20190228 MGI PMID:27383011 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004364 thin stria vascularis IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004364 thin stria vascularis IAGP N RGD:5509061 20170420 MGI PMID:26805784 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004365 abnormal strial basal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004366 abnormal strial marginal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004366 abnormal strial marginal cell morphology IAGP N RGD:5509061 20190228 MGI PMID:27383011 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004367 abnormal strial intermediate cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004368 abnormal stria vascularis vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004368 abnormal stria vascularis vasculature morphology IAGP N RGD:5509061 20190228 MGI PMID:27383011 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20170420 MGI PMID:26805784 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20190228 MGI PMID:27383011 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20190228 MGI PMID:27383011 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004427 abnormal vestibular labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004518 absent vestibular hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004897 otosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:11553273 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21642988 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21642988 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20170420 MGI PMID:19903857 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21642988 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:11553273 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20068174 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0006023 detached Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15138255 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20190228 MGI PMID:27383011 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17287522 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20170420 MGI PMID:19903857 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21642988 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20170420 MGI PMID:19903857 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0008308 small scala media IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20170420 MGI PMID:19903857 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20170420 MGI PMID:19903857 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21642988 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:20068174 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20068174 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12006579 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15138255 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15138255 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0011133 increased lung endothelial cell migration IAGP N RGD:5509061 20211125 MGI PMID:20068174 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:11553273 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16945494 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17284444 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20190228 MGI PMID:27383011 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0014378 increased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:11553273 68467 S1pr2 sphingosine-1-phosphate receptor 2 gene MP:0031434 increased miscarriage rate IAGP N RGD:5509061 20220915 MGI PMID:15138255 68469 Por cytochrome p450 oxidoreductase gene MP:0000296 absent trabeculae carneae IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12697746 68469 Por cytochrome p450 oxidoreductase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:12566435 68469 Por cytochrome p450 oxidoreductase gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:12566435 68469 Por cytochrome p450 oxidoreductase gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:12697746 68469 Por cytochrome p450 oxidoreductase gene MP:0000610 cholestasis IAGP N RGD:5509061 20150326 MGI PMID:25068656 68469 Por cytochrome p450 oxidoreductase gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15328377 68469 Por cytochrome p450 oxidoreductase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20375200 68469 Por cytochrome p450 oxidoreductase gene MP:0001263 weight loss IAGP N RGD:5509061 20150326 MGI PMID:25068656 68469 Por cytochrome p450 oxidoreductase gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:12697746 68469 Por cytochrome p450 oxidoreductase gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:12566435 68469 Por cytochrome p450 oxidoreductase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15328377 68469 Por cytochrome p450 oxidoreductase gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20375200 68469 Por cytochrome p450 oxidoreductase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12566435 68469 Por cytochrome p450 oxidoreductase gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12697746 68469 Por cytochrome p450 oxidoreductase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15328377 68469 Por cytochrome p450 oxidoreductase gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12566435 68469 Por cytochrome p450 oxidoreductase gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:15328377 68469 Por cytochrome p450 oxidoreductase gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:20375200 68469 Por cytochrome p450 oxidoreductase gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:15328377 68469 Por cytochrome p450 oxidoreductase gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:20375200 68469 Por cytochrome p450 oxidoreductase gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:12566435 68469 Por cytochrome p450 oxidoreductase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20150326 MGI PMID:25068656 68469 Por cytochrome p450 oxidoreductase gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20150326 MGI PMID:25068656 68469 Por cytochrome p450 oxidoreductase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:12697746 68469 Por cytochrome p450 oxidoreductase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20150326 MGI PMID:25068656 68469 Por cytochrome p450 oxidoreductase gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20150326 MGI PMID:25068656 68469 Por cytochrome p450 oxidoreductase gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20150326 MGI PMID:25068656 68469 Por cytochrome p450 oxidoreductase gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20150326 MGI PMID:25068656 68469 Por cytochrome p450 oxidoreductase gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:15328377 68469 Por cytochrome p450 oxidoreductase gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:20375200 68469 Por cytochrome p450 oxidoreductase gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20150326 MGI PMID:25068656 68469 Por cytochrome p450 oxidoreductase gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:12566435 68469 Por cytochrome p450 oxidoreductase gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20150326 MGI PMID:25068656 68469 Por cytochrome p450 oxidoreductase gene MP:0004838 abnormal neural fold elevation formation IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12566435 68469 Por cytochrome p450 oxidoreductase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12697746 68469 Por cytochrome p450 oxidoreductase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15328377 68469 Por cytochrome p450 oxidoreductase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20375200 68469 Por cytochrome p450 oxidoreductase gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:15328377 68469 Por cytochrome p450 oxidoreductase gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:20375200 68469 Por cytochrome p450 oxidoreductase gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:15328377 68469 Por cytochrome p450 oxidoreductase gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20150326 MGI PMID:25068656 68469 Por cytochrome p450 oxidoreductase gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20150326 MGI PMID:25068656 68469 Por cytochrome p450 oxidoreductase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:12697746 68469 Por cytochrome p450 oxidoreductase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:20375200 68469 Por cytochrome p450 oxidoreductase gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:20375200 68469 Por cytochrome p450 oxidoreductase gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:12566435 68469 Por cytochrome p450 oxidoreductase gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:15328377 68469 Por cytochrome p450 oxidoreductase gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12697746 68469 Por cytochrome p450 oxidoreductase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20150326 MGI PMID:25068656 68469 Por cytochrome p450 oxidoreductase gene MP:0009779 enhanced behavioral response to anesthetic IAGP N RGD:5509061 20141003 MGI PMID:20375200 68469 Por cytochrome p450 oxidoreductase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15328377 68469 Por cytochrome p450 oxidoreductase gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20375200 68469 Por cytochrome p450 oxidoreductase gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0012531 delayed limb development IAGP N RGD:5509061 20141003 MGI PMID:11742006 68469 Por cytochrome p450 oxidoreductase gene MP:0012691 abnormal acetaminophen metabolism IAGP N RGD:5509061 20161013 MGI PMID:12566435 68469 Por cytochrome p450 oxidoreductase gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:12566435 68469 Por cytochrome p450 oxidoreductase gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:12566435 68471 Pex14 peroxisomal biogenesis factor 14 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12904583 68471 Pex14 peroxisomal biogenesis factor 14 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 68473 Htt huntingtin gene MP:0000022 abnormal ear shape IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000023 abnormal ear position IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16403806 68473 Htt huntingtin gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16403806 68473 Htt huntingtin gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15935052 68473 Htt huntingtin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:10196365 68473 Htt huntingtin gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20150319 MGI PMID:23001568 68473 Htt huntingtin gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20150319 MGI PMID:23001568 68473 Htt huntingtin gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16697652 68473 Htt huntingtin gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000835 abnormal subthalamic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:7774020 68473 Htt huntingtin gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20151224 MGI PMID:25609071 68473 Htt huntingtin gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0001260 increased body weight IAGP N RGD:5509061 20150319 MGI PMID:23001568 68473 Htt huntingtin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17239451 68473 Htt huntingtin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19464370 68473 Htt huntingtin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0001263 weight loss IAGP N RGD:5509061 20151224 MGI PMID:25609071 68473 Htt huntingtin gene MP:0001263 weight loss IAGP N RGD:5509061 20200402 MGI PMID:28927719 68473 Htt huntingtin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11152661 68473 Htt huntingtin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:10196365 68473 Htt huntingtin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17239451 68473 Htt huntingtin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:7774020 68473 Htt huntingtin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0001400 hyperresponsive IAGP N RGD:5509061 20141003 MGI PMID:7774020 68473 Htt huntingtin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11152661 68473 Htt huntingtin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12223581 68473 Htt huntingtin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12926013 68473 Htt huntingtin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15935052 68473 Htt huntingtin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17239451 68473 Htt huntingtin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200402 MGI PMID:28927719 68473 Htt huntingtin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17018277 68473 Htt huntingtin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150319 MGI PMID:23001568 68473 Htt huntingtin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20151224 MGI PMID:25609071 68473 Htt huntingtin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200402 MGI PMID:28927719 68473 Htt huntingtin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11152661 68473 Htt huntingtin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12926013 68473 Htt huntingtin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200402 MGI PMID:28927719 68473 Htt huntingtin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:12926013 68473 Htt huntingtin gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0001407 short stride length IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20150319 MGI PMID:23001568 68473 Htt huntingtin gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:16403806 68473 Htt huntingtin gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:17239451 68473 Htt huntingtin gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20150319 MGI PMID:23001568 68473 Htt huntingtin gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20150319 MGI PMID:24728353 68473 Htt huntingtin gene MP:0001505 hunched posture IAGP N RGD:5509061 20200402 MGI PMID:28927719 68473 Htt huntingtin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:11152661 68473 Htt huntingtin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15935052 68473 Htt huntingtin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0001513 limb grasping IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:11152661 68473 Htt huntingtin gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:19464370 68473 Htt huntingtin gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:11152661 68473 Htt huntingtin gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:7618107 68473 Htt huntingtin gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:7774020 68473 Htt huntingtin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15496430 68473 Htt huntingtin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7618107 68473 Htt huntingtin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7774020 68473 Htt huntingtin gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:7618107 68473 Htt huntingtin gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:7550343 68473 Htt huntingtin gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:7774020 68473 Htt huntingtin gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20150319 MGI PMID:24728353 68473 Htt huntingtin gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11133364 68473 Htt huntingtin gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:7774020 68473 Htt huntingtin gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:11152661 68473 Htt huntingtin gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12926013 68473 Htt huntingtin gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20150319 MGI PMID:23001568 68473 Htt huntingtin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11152661 68473 Htt huntingtin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:7618107 68473 Htt huntingtin gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11160912 68473 Htt huntingtin gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7550343 68473 Htt huntingtin gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7618107 68473 Htt huntingtin gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7550343 68473 Htt huntingtin gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7618107 68473 Htt huntingtin gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7774020 68473 Htt huntingtin gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12926013 68473 Htt huntingtin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11160912 68473 Htt huntingtin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7618107 68473 Htt huntingtin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:11152661 68473 Htt huntingtin gene MP:0002183 gliosis IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20150319 MGI PMID:24728353 68473 Htt huntingtin gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12223581 68473 Htt huntingtin gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12926013 68473 Htt huntingtin gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:7550343 68473 Htt huntingtin gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11133364 68473 Htt huntingtin gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:17239451 68473 Htt huntingtin gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20150319 MGI PMID:23001568 68473 Htt huntingtin gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20200402 MGI PMID:28927719 68473 Htt huntingtin gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20150319 MGI PMID:23001568 68473 Htt huntingtin gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20200402 MGI PMID:28927719 68473 Htt huntingtin gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20150319 MGI PMID:24728353 68473 Htt huntingtin gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:7550343 68473 Htt huntingtin gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16403806 68473 Htt huntingtin gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:11133364 68473 Htt huntingtin gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:11152661 68473 Htt huntingtin gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:17018277 68473 Htt huntingtin gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:17239451 68473 Htt huntingtin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:11494364 68473 Htt huntingtin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20150319 MGI PMID:23001568 68473 Htt huntingtin gene MP:0003382 straub tail IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15935052 68473 Htt huntingtin gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:16403806 68473 Htt huntingtin gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0003895 increased ectoderm apoptosis IAGP N RGD:5509061 20141003 MGI PMID:7618107 68473 Htt huntingtin gene MP:0003954 abnormal Reichert's membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:7550343 68473 Htt huntingtin gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11160912 68473 Htt huntingtin gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:7550343 68473 Htt huntingtin gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:11152661 68473 Htt huntingtin gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:10699173 68473 Htt huntingtin gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:12223581 68473 Htt huntingtin gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:16697652 68473 Htt huntingtin gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:17018277 68473 Htt huntingtin gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20150319 MGI PMID:23001568 68473 Htt huntingtin gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20151224 MGI PMID:25609071 68473 Htt huntingtin gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20200402 MGI PMID:28927719 68473 Htt huntingtin gene MP:0004081 abnormal globus pallidus morphology IAGP N RGD:5509061 20141003 MGI PMID:7774020 68473 Htt huntingtin gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0004103 abnormal ventral striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:10699173 68473 Htt huntingtin gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:11152661 68473 Htt huntingtin gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:12554681 68473 Htt huntingtin gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20151224 MGI PMID:25609071 68473 Htt huntingtin gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:10533044 68473 Htt huntingtin gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:15935052 68473 Htt huntingtin gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17715336 68473 Htt huntingtin gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20150319 MGI PMID:24728353 68473 Htt huntingtin gene MP:0005405 axon degeneration IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0005499 abnormal olfactory system morphology IAGP N RGD:5509061 20141003 MGI PMID:12926013 68473 Htt huntingtin gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16403806 68473 Htt huntingtin gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20210121 MGI PMID:32876667 68473 Htt huntingtin gene MP:0006323 abnormal extraembryonic mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:7618107 68473 Htt huntingtin gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:11133364 68473 Htt huntingtin gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:11160912 68473 Htt huntingtin gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:15496430 68473 Htt huntingtin gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:11062468 68473 Htt huntingtin gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11133364 68473 Htt huntingtin gene MP:0008402 increased cellular sensitivity to alkylating agents IAGP N RGD:5509061 20210121 MGI PMID:32876667 68473 Htt huntingtin gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10699173 68473 Htt huntingtin gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20151224 MGI PMID:25609071 68473 Htt huntingtin gene MP:0008918 microgliosis IAGP N RGD:5509061 20151224 MGI PMID:25609071 68473 Htt huntingtin gene MP:0009324 absent hippocampal fimbria IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:7618107 68473 Htt huntingtin gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20151224 MGI PMID:25609071 68473 Htt huntingtin gene MP:0009964 abnormal cerebellum lobule morphology IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0010052 increased grip strength IEA N RGD:5509061 20230119 MGI 68473 Htt huntingtin gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200402 MGI PMID:28927719 68473 Htt huntingtin gene MP:0010540 long stride length IAGP N RGD:5509061 20200402 MGI PMID:28927719 68473 Htt huntingtin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200402 MGI PMID:28927719 68473 Htt huntingtin gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7550343 68473 Htt huntingtin gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11160912 68473 Htt huntingtin gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7618107 68473 Htt huntingtin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7774020 68473 Htt huntingtin gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20200402 MGI PMID:28927719 68473 Htt huntingtin gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7774020 68473 Htt huntingtin gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9398841 68473 Htt huntingtin gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:7550343 68473 Htt huntingtin gene MP:0011191 increased embryonic epiblast cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:7550343 68473 Htt huntingtin gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:7550343 68473 Htt huntingtin gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20150319 MGI PMID:24728353 68473 Htt huntingtin gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20151224 MGI PMID:25609071 68473 Htt huntingtin gene MP:0011975 neuronal cytoplasmic inclusions IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0012095 increased Reichert's membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:7550343 68473 Htt huntingtin gene MP:0012104 small amniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:7550343 68473 Htt huntingtin gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:7618107 68473 Htt huntingtin gene MP:0012165 absent neural folds IAGP N RGD:5509061 20141003 MGI PMID:15496430 68473 Htt huntingtin gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20150319 MGI PMID:23001568 68473 Htt huntingtin gene MP:0012448 abnormal primary motor cortex morphology IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0012506 brain atrophy IAGP N RGD:5509061 20151224 MGI PMID:25609071 68473 Htt huntingtin gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230119 MGI 68473 Htt huntingtin gene MP:0013438 dysmyelination IAGP N RGD:5509061 20151224 MGI PMID:25609071 68473 Htt huntingtin gene MP:0013438 dysmyelination IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:7550343 68473 Htt huntingtin gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:24728353 68473 Htt huntingtin gene MP:0020070 decreased neocortex volume IAGP N RGD:5509061 20151224 MGI PMID:25609071 68473 Htt huntingtin gene MP:0020214 increased susceptibility to malignant hyperthermia IAGP N RGD:5509061 20141003 MGI PMID:11709539 68473 Htt huntingtin gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:11133364 68473 Htt huntingtin gene MP:0030635 increased taurine level IAGP N RGD:5509061 20180913 MGI PMID:25609071 68473 Htt huntingtin gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20220519 MGI PMID:27623015 68473 Htt huntingtin gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:12926013 68473 Htt huntingtin gene MP:0031442 enlarged cerebral aqueduct IAGP N RGD:5509061 20221103 MGI PMID:9398841 68476 Fads2 fatty acid desaturase 2 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0002223 lymphoid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220407 MGI PMID:21653892 68476 Fads2 fatty acid desaturase 2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0003356 impaired luteinization IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0003696 abnormal zona pellucida morphology IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0003697 absent zona pellucida IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0005285 decreased unsaturated fatty acids level IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20220407 MGI PMID:21653892 68476 Fads2 fatty acid desaturase 2 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20220407 MGI PMID:21653892 68476 Fads2 fatty acid desaturase 2 gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0009368 absent theca folliculi IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20180621 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20220407 MGI PMID:21653892 68476 Fads2 fatty acid desaturase 2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:19351970 68476 Fads2 fatty acid desaturase 2 gene MP:0020111 decreased thromboxane level IAGP N RGD:5509061 20201001 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0030980 abnormal acroplaxome morphology IAGP N RGD:5509061 20220407 MGI PMID:21653892 68476 Fads2 fatty acid desaturase 2 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201001 MGI PMID:19172737 68476 Fads2 fatty acid desaturase 2 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220407 MGI PMID:21653892 68476 Fads2 fatty acid desaturase 2 gene MP:0031355 abnormal proacrosomal vesicle fusion IAGP N RGD:5509061 20220407 MGI PMID:21653892 68479 Pik3r2 phosphoinositide-3-kinase regulatory subunit 2 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20231005 MGI PMID:32856318 68479 Pik3r2 phosphoinositide-3-kinase regulatory subunit 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 68479 Pik3r2 phosphoinositide-3-kinase regulatory subunit 2 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20231005 MGI PMID:32856318 68479 Pik3r2 phosphoinositide-3-kinase regulatory subunit 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11752399 68479 Pik3r2 phosphoinositide-3-kinase regulatory subunit 2 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:16227599 68479 Pik3r2 phosphoinositide-3-kinase regulatory subunit 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11752399 68479 Pik3r2 phosphoinositide-3-kinase regulatory subunit 2 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20231005 MGI PMID:32856318 68479 Pik3r2 phosphoinositide-3-kinase regulatory subunit 2 gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:16227599 68479 Pik3r2 phosphoinositide-3-kinase regulatory subunit 2 gene MP:0005238 increased brain size IAGP N RGD:5509061 20231005 MGI PMID:32856318 68479 Pik3r2 phosphoinositide-3-kinase regulatory subunit 2 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20160804 MGI 68479 Pik3r2 phosphoinositide-3-kinase regulatory subunit 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11752399 68479 Pik3r2 phosphoinositide-3-kinase regulatory subunit 2 gene MP:0005603 neuron hypertrophy IAGP N RGD:5509061 20231005 MGI PMID:32856318 68479 Pik3r2 phosphoinositide-3-kinase regulatory subunit 2 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19029981 68479 Pik3r2 phosphoinositide-3-kinase regulatory subunit 2 gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19029981 68479 Pik3r2 phosphoinositide-3-kinase regulatory subunit 2 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20231005 MGI PMID:32856318 68480 Slc7a3 solute carrier family 7 (cationic amino acid transporter, y+ system), member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230323 MGI PMID:36528691 68485 Hspb3 heat shock protein 3 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20210128 MGI 68485 Hspb3 heat shock protein 3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 68489 Celf2 CUGBP, Elav-like family member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190620 MGI PMID:27253061 68489 Celf2 CUGBP, Elav-like family member 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20190620 MGI PMID:27253061 68489 Celf2 CUGBP, Elav-like family member 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20190620 MGI PMID:27253061 68489 Celf2 CUGBP, Elav-like family member 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20190620 MGI PMID:27253061 68489 Celf2 CUGBP, Elav-like family member 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20190620 MGI PMID:27253061 68489 Celf2 CUGBP, Elav-like family member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 68491 Scamp2 secretory carrier membrane protein 2 gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 68491 Scamp2 secretory carrier membrane protein 2 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 68491 Scamp2 secretory carrier membrane protein 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20201022 MGI 68491 Scamp2 secretory carrier membrane protein 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 68491 Scamp2 secretory carrier membrane protein 2 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 68491 Scamp2 secretory carrier membrane protein 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 68491 Scamp2 secretory carrier membrane protein 2 gene MP:0012121 sclerocornea IEA N RGD:5509061 20201231 MGI 68491 Scamp2 secretory carrier membrane protein 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8563022 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0000653 abnormal sex gland morphology IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:8563022 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001116 small gonad IAGP N RGD:5509061 20191114 MGI PMID:27833742 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:21820362 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20191114 MGI PMID:27833742 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001147 small testis IAGP N RGD:5509061 20191114 MGI PMID:27833742 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:21820362 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:21820362 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7491115 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:21820362 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21820362 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:21820362 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:7479914 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:8187173 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:8563022 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20191114 MGI PMID:27833742 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7491115 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:7491115 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22987798 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:12727442 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:7479914 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:8187173 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:8563022 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:8563022 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21820362 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:21820362 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20191114 MGI PMID:27833742 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0003379 absent sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0003379 absent sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0003379 absent sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0003578 absent ovary IAGP N RGD:5509061 20141003 MGI PMID:7479914 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0003578 absent ovary IAGP N RGD:5509061 20141003 MGI PMID:7491115 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0003578 absent ovary IAGP N RGD:5509061 20141003 MGI PMID:8187173 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0003578 absent ovary IAGP N RGD:5509061 20141003 MGI PMID:8563022 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:21820362 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:21820362 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21820362 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005147 prostate gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005147 prostate gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005148 seminal vesicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005148 seminal vesicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005158 ovary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005158 ovary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005158 ovary hypoplasia IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20141003 MGI PMID:7479914 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20141003 MGI PMID:7491115 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20141003 MGI PMID:8187173 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20141003 MGI PMID:8563022 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20191114 MGI PMID:27833742 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:11416865 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005644 agonadal IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005644 agonadal IAGP N RGD:5509061 20141003 MGI PMID:7479914 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005644 agonadal IAGP N RGD:5509061 20141003 MGI PMID:7491115 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005644 agonadal IAGP N RGD:5509061 20141003 MGI PMID:8187173 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0005644 agonadal IAGP N RGD:5509061 20141003 MGI PMID:8563022 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0006415 absent testes IAGP N RGD:5509061 20141003 MGI PMID:7479914 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0006415 absent testes IAGP N RGD:5509061 20141003 MGI PMID:7491115 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0006415 absent testes IAGP N RGD:5509061 20141003 MGI PMID:8187173 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0006415 absent testes IAGP N RGD:5509061 20141003 MGI PMID:8563022 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0006418 abnormal testis cord formation IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0008257 thin myometrium IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0008293 abnormal adrenal gland zona glomerulosa morphology IAGP N RGD:5509061 20141003 MGI PMID:24035414 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0008297 retention of the adrenal gland x-zone IAGP N RGD:5509061 20141120 MGI PMID:21820362 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0008335 decreased gonadotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:8563022 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20220609 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0009018 short estrus IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0009094 abnormal endometrial gland morphology IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0009096 decreased endometrial gland number IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0009203 external male genitalia hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0009207 internal male genitalia hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0009207 internal male genitalia hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20141003 MGI PMID:15118069 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:12727442 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7479914 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7491115 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8187173 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8563022 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20191114 MGI PMID:27833742 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7491115 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11124111 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0011384 abnormal progesterone level IAGP N RGD:5509061 20141003 MGI PMID:21820362 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20141003 MGI PMID:21820362 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0011411 abnormal gonadal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:8187173 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0011415 abnormal aldosterone level IAGP N RGD:5509061 20141120 MGI PMID:21820362 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0013400 abnormal endometrial gland development IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0020556 abnormal ventromedial hypothalamic nucleus morphology IAGP N RGD:5509061 20180315 MGI PMID:12727442 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0020558 decreased ventromedial hypothalamic nucleus size IAGP N RGD:5509061 20180315 MGI PMID:8563022 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0031018 decreased granulosa cell proliferation IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220609 MGI PMID:18703422 68494 Nr5a1 nuclear receptor subfamily 5, group A, member 1 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:18703422 68498 Dhodh dihydroorotate dehydrogenase gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 68498 Dhodh dihydroorotate dehydrogenase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 68498 Dhodh dihydroorotate dehydrogenase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 68498 Dhodh dihydroorotate dehydrogenase gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20150101 MGI PMID:25176150 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:15327767 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17670946 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:17670946 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0001652 colonic necrosis IAGP N RGD:5509061 20141003 MGI PMID:17670946 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:15831456 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:15014077 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:15014077 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:15831456 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:15014077 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15831456 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17670946 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17409375 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20150101 MGI PMID:25176150 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17289919 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:17908794 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20150101 MGI PMID:25176150 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20150101 MGI PMID:25176150 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:18323469 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:14766742 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:17908794 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:17409375 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:17289919 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:17289919 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15014077 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18323469 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:17409375 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20150101 MGI PMID:25176150 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20150101 MGI PMID:25176150 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:17908794 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20150101 MGI PMID:25176150 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18323469 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:17670946 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:17409375 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20150101 MGI PMID:25176150 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15327767 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15014077 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15831456 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15831456 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15831456 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15831456 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0011197 abnormal proamniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:15831456 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0011199 abnormal amniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:15014077 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0012142 absent amniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:15014077 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0012224 abnormal sterol level IAGP N RGD:5509061 20150101 MGI PMID:25176150 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0014476 abnormal feces lipid level IAGP N RGD:5509061 20240704 MGI PMID:17908794 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0014476 abnormal feces lipid level IAGP N RGD:5509061 20240704 MGI PMID:25176150 68500 Nr5a2 nuclear receptor subfamily 5, group A, member 2 gene MP:0014478 increased feces bile salt level IAGP N RGD:5509061 20240704 MGI PMID:17908794 68503 Cubn cubilin gene MP:0001307 fused cornea and lens IEA N RGD:5509061 20210128 MGI 68503 Cubn cubilin gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20210128 MGI 68503 Cubn cubilin gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:16787536 68503 Cubn cubilin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16787536 68503 Cubn cubilin gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:16787536 68503 Cubn cubilin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16787536 68503 Cubn cubilin gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16787536 68503 Cubn cubilin gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:20798259 68503 Cubn cubilin gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:20798259 68503 Cubn cubilin gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:16787536 68503 Cubn cubilin gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16787536 68503 Cubn cubilin gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:16787536 68503 Cubn cubilin gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:16787536 68503 Cubn cubilin gene MP:0004222 iris synechia IEA N RGD:5509061 20210128 MGI 68503 Cubn cubilin gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:16787536 68503 Cubn cubilin gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:16787536 68503 Cubn cubilin gene MP:0009593 absent chorion IAGP N RGD:5509061 20141003 MGI PMID:16787536 68503 Cubn cubilin gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:20798259 68503 Cubn cubilin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20798259 68503 Cubn cubilin gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20798259 68503 Cubn cubilin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16787536 68503 Cubn cubilin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 68503 Cubn cubilin gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16787536 68503 Cubn cubilin gene MP:0011227 abnormal vitamin B12 level IAGP N RGD:5509061 20141003 MGI PMID:20798259 68504 Scamp5 secretory carrier membrane protein 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 68504 Scamp5 secretory carrier membrane protein 5 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20200730 MGI PMID:32020363 68504 Scamp5 secretory carrier membrane protein 5 gene MP:0002064 seizures IAGP N RGD:5509061 20200730 MGI PMID:32020363 68504 Scamp5 secretory carrier membrane protein 5 gene MP:0002083 premature death IAGP N RGD:5509061 20200730 MGI PMID:32020363 68504 Scamp5 secretory carrier membrane protein 5 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 68504 Scamp5 secretory carrier membrane protein 5 gene MP:0002959 increased urine microalbumin level IEA N RGD:5509061 20211021 MGI 68504 Scamp5 secretory carrier membrane protein 5 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 68504 Scamp5 secretory carrier membrane protein 5 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20200730 MGI PMID:32020363 68504 Scamp5 secretory carrier membrane protein 5 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20200730 MGI PMID:32020363 68504 Scamp5 secretory carrier membrane protein 5 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20181227 MGI 68504 Scamp5 secretory carrier membrane protein 5 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20200730 MGI PMID:32020363 68504 Scamp5 secretory carrier membrane protein 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 68504 Scamp5 secretory carrier membrane protein 5 gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20200730 MGI PMID:32020363 68504 Scamp5 secretory carrier membrane protein 5 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20201231 MGI 68504 Scamp5 secretory carrier membrane protein 5 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0000440 domed cranium IAGP N RGD:5509061 20170309 MGI PMID:27336173 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210520 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0000774 decreased brain size IAGP N RGD:5509061 20170309 MGI PMID:27336173 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20170309 MGI PMID:27336173 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20210826 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0001200 thick skin IEA N RGD:5509061 20210826 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170309 MGI PMID:27336173 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20170309 MGI PMID:27336173 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20170309 MGI PMID:27336173 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210128 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0002175 decreased brain weight IEA N RGD:5509061 20220811 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0002188 small heart IEA N RGD:5509061 20210128 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20170309 MGI PMID:27336173 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20221215 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0002834 decreased heart weight IEA N RGD:5509061 20210520 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20170309 MGI PMID:27336173 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0003883 enlarged stomach IEA N RGD:5509061 20210520 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20221215 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20210520 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20170309 MGI PMID:27336173 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0008283 small hippocampus IAGP N RGD:5509061 20170309 MGI PMID:27336173 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210826 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20170309 MGI PMID:27336173 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20170309 MGI PMID:27336173 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20170309 MGI PMID:27336173 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0011069 abnormal brain ependyma motile cilium physiology IAGP N RGD:5509061 20170309 MGI PMID:27336173 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0011940 decreased food intake IEA N RGD:5509061 20230601 MGI 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0013907 abnormal cerebrospinal fluid flow IAGP N RGD:5509061 20170309 MGI PMID:27336173 68506 Pdcd6ip programmed cell death 6 interacting protein gene MP:0030963 abnormal brain ependyma motile cilium location or orientation IAGP N RGD:5509061 20190725 MGI PMID:27336173 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:16533945 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11516952 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16533944 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0000692 small spleen IEA N RGD:5509061 20181227 MGI 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11682618 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12626748 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20200402 MGI 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12626748 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16533945 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16533945 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:12626748 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11682618 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11682618 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16533945 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11682618 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11682618 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16533945 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11682618 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:11682618 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12626748 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0002989 small kidney IEA N RGD:5509061 20181227 MGI 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16533945 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:11682618 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17325031 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16533944 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:11516952 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:16533945 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:21156286 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11682618 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11682618 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11682618 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12626748 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20240523 MGI 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20240523 MGI 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:11682618 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:12626748 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20180614 MGI PMID:12626748 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:16533945 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20181227 MGI 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16533944 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17325031 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16533945 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20180614 MGI PMID:12626748 68512 Pttg1 pituitary tumor-transforming gene 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20180614 MGI PMID:12626748 68513 Dbil5 diazepam binding inhibitor-like 5 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 68513 Dbil5 diazepam binding inhibitor-like 5 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20211021 MGI 68513 Dbil5 diazepam binding inhibitor-like 5 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 68514 Lxn latexin gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:16469302 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:18296659 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:16174770 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:21224384 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:21224384 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16174770 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16174770 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:16174770 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18055784 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18296659 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:18296659 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:18296659 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21224384 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:23221340 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18296659 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21224384 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21224384 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21224384 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:23221340 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:18055784 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:18296659 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0009257 dilated seminiferous tubule IAGP N RGD:5509061 20141003 MGI PMID:16174770 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0011232 abnormal vitamin A level IAGP N RGD:5509061 20141003 MGI PMID:16174770 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0011232 abnormal vitamin A level IAGP N RGD:5509061 20141003 MGI PMID:18055784 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0011233 abnormal vitamin A metabolism IAGP N RGD:5509061 20141003 MGI PMID:14684738 68516 Lrat lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) gene MP:0011234 abnormal retinol level IAGP N RGD:5509061 20141003 MGI PMID:16174770 68518 Hal histidine ammonia lyase gene MP:0011654 histidinuria IAGP N RGD:5509061 20141003 MGI PMID:15287859 68520 Sigmar1 sigma non-opioid intracellular receptor 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 68520 Sigmar1 sigma non-opioid intracellular receptor 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:14622179 68520 Sigmar1 sigma non-opioid intracellular receptor 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20167253 68520 Sigmar1 sigma non-opioid intracellular receptor 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:20167253 68520 Sigmar1 sigma non-opioid intracellular receptor 1 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:19100292 68524 Grid1 glutamate receptor, ionotropic, delta 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17438141 68524 Grid1 glutamate receptor, ionotropic, delta 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17438141 68524 Grid1 glutamate receptor, ionotropic, delta 1 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:17438141 68524 Grid1 glutamate receptor, ionotropic, delta 1 gene MP:0004490 type IV spiral ligament fibrocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:17438141 68524 Grid1 glutamate receptor, ionotropic, delta 1 gene MP:0004597 increased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20141003 MGI PMID:17438141 68524 Grid1 glutamate receptor, ionotropic, delta 1 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:17438141 68524 Grid1 glutamate receptor, ionotropic, delta 1 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:17438141 68524 Grid1 glutamate receptor, ionotropic, delta 1 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17438141 68524 Grid1 glutamate receptor, ionotropic, delta 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:17438141 68524 Grid1 glutamate receptor, ionotropic, delta 1 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20240523 MGI 68524 Grid1 glutamate receptor, ionotropic, delta 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17438141 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0000622 increased salivation IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16135092 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0001437 no swallowing reflex IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:18713855 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:18713855 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11517215 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0001937 abnormal sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:11517215 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:16135092 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18713855 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18713855 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0005320 abnormal biopterin level IAGP N RGD:5509061 20141003 MGI PMID:11517215 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0005320 abnormal biopterin level IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0005320 abnormal biopterin level IAGP N RGD:5509061 20141003 MGI PMID:16135092 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0005321 abnormal neopterin level IAGP N RGD:5509061 20141003 MGI PMID:11517215 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0005321 abnormal neopterin level IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0005321 abnormal neopterin level IAGP N RGD:5509061 20141003 MGI PMID:16135092 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:18713855 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11517215 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:11517215 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:11517215 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:16135092 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11517215 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12734191 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16135092 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20180920 MGI PMID:11517215 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0030671 decreased circulating phenylalanine level IAGP N RGD:5509061 20180920 MGI PMID:16135092 68526 Pts 6-pyruvoyl-tetrahydropterin synthase gene MP:0030697 increased phenylalanine level IAGP N RGD:5509061 20180920 MGI PMID:11517215 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:1689261 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000436 abnormal head movements IEA N RGD:5509061 20111116 MGI 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000743 muscle spasm IEA N RGD:5509061 20111116 MGI 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000745 tremors IEA N RGD:5509061 20111116 MGI 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9065501 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:11739579 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:18551174 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:22279216 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:2400906 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:9065501 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20161013 MGI PMID:12628171 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:9271665 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:12628171 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:10804210 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:18551174 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12628171 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:22279216 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9065501 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9271665 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10804210 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11672610 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12628171 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15728855 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17978051 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18551174 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22279216 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:2400906 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7736576 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:10804210 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:2077109 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10804210 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11672610 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12628171 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:2400906 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:11739579 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:22279216 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:2400906 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:11739579 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9065501 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000911 abnormal trigeminal motor nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9065501 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0000920 abnormal myelination IEA N RGD:5509061 20111116 MGI 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18551174 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001389 abnormal eye movement IAGP N RGD:5509061 20141003 MGI PMID:15014119 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001389 abnormal eye movement IAGP N RGD:5509061 20141003 MGI PMID:15813941 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001389 abnormal eye movement IAGP N RGD:5509061 20150521 MGI PMID:24078737 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10804210 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11672610 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12628171 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12752376 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:1689261 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18249497 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18551174 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20231872 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:7736576 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9065501 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9271665 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20150521 MGI PMID:24078737 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:9767169 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:7736576 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11672610 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15014119 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18249497 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20231872 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:7736576 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12752376 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:1689261 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18551174 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:2400906 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:7736576 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9271665 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:2400906 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001408 stereotypic behavior IEA N RGD:5509061 20111116 MGI 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:9767169 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9065501 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001440 abnormal grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:9661982 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:8848495 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:17978051 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:2400906 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:9271665 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:2400906 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:20231872 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:7736576 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20150507 MGI PMID:7914819 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:8742448 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11672610 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:2400906 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001527 athetotic walking movements IEA N RGD:5509061 20111116 MGI 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:9387853 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:9387853 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:7766857 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:1689261 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:1689261 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:15813941 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20111116 MGI 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:2400906 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002082 postnatal lethality IEA N RGD:5509061 20111116 MGI 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002204 abnormal synaptic neurotransmitter level IAGP N RGD:5509061 20150507 MGI PMID:7914819 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15574740 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17978051 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:21628556 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:7736576 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002566 abnormal sexual interaction IEA N RGD:5509061 20111116 MGI 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:1689261 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:7736576 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002802 abnormal discrimination learning IAGP N RGD:5509061 20141003 MGI PMID:8402174 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:11672610 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:18551174 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002807 abnormal eye blink conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11285022 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002807 abnormal eye blink conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11722613 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21628556 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:11739579 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17978051 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21628556 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:11672610 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:7736576 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20141003 MGI PMID:11672610 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20141003 MGI PMID:11739579 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20141003 MGI PMID:7736576 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:15574740 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11672610 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0004814 reduced linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0004844 abnormal vestibuloocular reflex IAGP N RGD:5509061 20141003 MGI PMID:15813941 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:11672610 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:18551174 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:2400906 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:7736576 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:18551174 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:9271665 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:18551174 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:8742448 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:8742448 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0005202 lethargy IEA N RGD:5509061 20111116 MGI 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:15014119 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:9383282 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:12628171 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:10804210 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:11672610 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18249497 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18551174 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22279216 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:2400906 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0008770 decreased survivor rate IEA N RGD:5509061 20111116 MGI 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:1689261 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0008913 weaving IAGP N RGD:5509061 20141003 MGI PMID:9271665 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0008921 increased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:22279216 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:10804210 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:11488959 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0009393 abnormal resting posture IEA N RGD:5509061 20111116 MGI 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0009514 titubation IAGP N RGD:5509061 20141003 MGI PMID:9271665 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:18249497 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:9065501 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20141003 MGI PMID:15813941 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:9065501 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:10804210 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:12628171 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0009964 abnormal cerebellum lobule morphology IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0010323 retropulsion IAGP N RGD:5509061 20141003 MGI PMID:2400906 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9271665 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9065501 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9271665 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0011267 abnormal excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:22279216 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0011271 prolonged excitatory postsynaptic current rise time IAGP N RGD:5509061 20240418 MGI PMID:17978051 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0011271 prolonged excitatory postsynaptic current rise time IAGP N RGD:5509061 20240418 MGI PMID:21628556 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0011273 prolonged excitatory postsynaptic current decay time IAGP N RGD:5509061 20240418 MGI PMID:17978051 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0011273 prolonged excitatory postsynaptic current decay time IAGP N RGD:5509061 20240418 MGI PMID:21628556 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20141003 MGI 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0012490 abnormal cochlear VIII nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:2077109 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20160714 MGI PMID:25250835 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:10804210 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:12628171 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:2400906 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0014331 abnormal Purkinje cell mitochondrial morphology IAGP N RGD:5509061 20240718 MGI PMID:18551174 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0014384 increased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:15574740 68528 Grid2 glutamate receptor, ionotropic, delta 2 gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:1689261 68530 Rab11b RAB11B, member RAS oncogene family gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 68530 Rab11b RAB11B, member RAS oncogene family gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 68530 Rab11b RAB11B, member RAS oncogene family gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210422 MGI 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0000274 enlarged heart IEA N RGD:5509061 20210422 MGI 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0001297 microphthalmia IEA N RGD:5509061 20221103 MGI 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20141003 MGI 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0001304 cataract IEA N RGD:5509061 20141003 MGI 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19323847 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221103 MGI 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0001785 edema IEA N RGD:5509061 20221103 MGI 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:19323847 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0002833 increased heart weight IEA N RGD:5509061 20221215 MGI 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0003136 yellow coat color IEA N RGD:5509061 20141003 MGI 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:19323847 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:19323847 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:19323847 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20210422 MGI 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0009709 hydrometra IEA N RGD:5509061 20210422 MGI 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19323847 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:19323847 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210422 MGI 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0013908 small lateral ventricles IAGP N RGD:5509061 20161103 MGI PMID:19323847 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0030644 increased circulating methionine level IAGP N RGD:5509061 20180927 MGI PMID:19323847 68532 Tdo2 tryptophan 2,3-dioxygenase gene MP:0030703 increased circulating threonine level IAGP N RGD:5509061 20180927 MGI PMID:19323847 68534 Mtor mechanistic target of rapamycin kinase gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 68534 Mtor mechanistic target of rapamycin kinase gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 68534 Mtor mechanistic target of rapamycin kinase gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0000274 enlarged heart IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22193387 68534 Mtor mechanistic target of rapamycin kinase gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:10079223 68534 Mtor mechanistic target of rapamycin kinase gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10079223 68534 Mtor mechanistic target of rapamycin kinase gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10079223 68534 Mtor mechanistic target of rapamycin kinase gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:10079223 68534 Mtor mechanistic target of rapamycin kinase gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:22302821 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22302821 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:22302821 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24336796 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:22302821 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:19185849 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:15254238 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10079223 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11707573 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10079223 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11707573 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11707573 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15485918 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22193387 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002083 premature death IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:15485918 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11707573 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15485918 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15485918 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:20388826 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19538929 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15485918 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:15485918 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:22193387 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:22193387 68534 Mtor mechanistic target of rapamycin kinase gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:22302821 68534 Mtor mechanistic target of rapamycin kinase gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:19538929 68534 Mtor mechanistic target of rapamycin kinase gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:20388826 68534 Mtor mechanistic target of rapamycin kinase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10079223 68534 Mtor mechanistic target of rapamycin kinase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11707573 68534 Mtor mechanistic target of rapamycin kinase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15485918 68534 Mtor mechanistic target of rapamycin kinase gene MP:0004036 abnormal muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10079223 68534 Mtor mechanistic target of rapamycin kinase gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:20388826 68534 Mtor mechanistic target of rapamycin kinase gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:15485918 68534 Mtor mechanistic target of rapamycin kinase gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19538929 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15254238 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15485918 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17141160 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19538929 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005324 ascites IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:22193387 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22193387 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22302821 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20160804 MGI 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24336796 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:22193387 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19538929 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19538929 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:19538929 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19538929 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:20388826 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:22302821 68534 Mtor mechanistic target of rapamycin kinase gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:19538929 68534 Mtor mechanistic target of rapamycin kinase gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:24336796 68534 Mtor mechanistic target of rapamycin kinase gene MP:0009341 decreased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22193387 68534 Mtor mechanistic target of rapamycin kinase gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20388826 68534 Mtor mechanistic target of rapamycin kinase gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:20388826 68534 Mtor mechanistic target of rapamycin kinase gene MP:0010334 pleural effusion IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0010738 abnormal internode morphology IAGP N RGD:5509061 20141003 MGI PMID:22302821 68534 Mtor mechanistic target of rapamycin kinase gene MP:0010739 abnormal axolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:22302821 68534 Mtor mechanistic target of rapamycin kinase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22193387 68534 Mtor mechanistic target of rapamycin kinase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10079223 68534 Mtor mechanistic target of rapamycin kinase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15254238 68534 Mtor mechanistic target of rapamycin kinase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15485918 68534 Mtor mechanistic target of rapamycin kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 68534 Mtor mechanistic target of rapamycin kinase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:22193387 68534 Mtor mechanistic target of rapamycin kinase gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:15254238 68534 Mtor mechanistic target of rapamycin kinase gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:17141160 68534 Mtor mechanistic target of rapamycin kinase gene MP:0013272 abnormal translation IAGP N RGD:5509061 20161208 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0013906 absent embryonic telencephalon IAGP N RGD:5509061 20150924 MGI PMID:10079223 68534 Mtor mechanistic target of rapamycin kinase gene MP:0013906 absent embryonic telencephalon IAGP N RGD:5509061 20150924 MGI PMID:11707573 68534 Mtor mechanistic target of rapamycin kinase gene MP:0014274 decreased respiration IAGP N RGD:5509061 20230810 MGI PMID:20008564 68534 Mtor mechanistic target of rapamycin kinase gene MP:0014472 impaired B cell migration IAGP N RGD:5509061 20240613 MGI PMID:21079150 68534 Mtor mechanistic target of rapamycin kinase gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:20644257 68534 Mtor mechanistic target of rapamycin kinase gene MP:0021206 abnormal limb muscle morphology IAGP N RGD:5509061 20221201 MGI PMID:20008564 68536 Ctbp2 C-terminal binding protein 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20221215 MGI 68536 Ctbp2 C-terminal binding protein 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20221215 MGI 68536 Ctbp2 C-terminal binding protein 2 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 68536 Ctbp2 C-terminal binding protein 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20221215 MGI 68536 Ctbp2 C-terminal binding protein 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20221215 MGI 68536 Ctbp2 C-terminal binding protein 2 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0001785 edema IEA N RGD:5509061 20221215 MGI 68536 Ctbp2 C-terminal binding protein 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 68536 Ctbp2 C-terminal binding protein 2 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:12101226 68536 Ctbp2 C-terminal binding protein 2 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20210826 MGI 68538 Ruvbl1 RuvB-like AAA ATPase 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20160505 MGI PMID:22371176 68538 Ruvbl1 RuvB-like AAA ATPase 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 68538 Ruvbl1 RuvB-like AAA ATPase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20160505 MGI PMID:22371176 68538 Ruvbl1 RuvB-like AAA ATPase 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20160505 MGI PMID:22371176 68538 Ruvbl1 RuvB-like AAA ATPase 1 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20160505 MGI PMID:22371176 68538 Ruvbl1 RuvB-like AAA ATPase 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20160505 MGI PMID:22371176 68538 Ruvbl1 RuvB-like AAA ATPase 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20160505 MGI PMID:22371176 68538 Ruvbl1 RuvB-like AAA ATPase 1 gene MP:0011695 absent hematopoietic stem cells IAGP N RGD:5509061 20160505 MGI PMID:22371176 68538 Ruvbl1 RuvB-like AAA ATPase 1 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20160505 MGI PMID:22371176 68538 Ruvbl1 RuvB-like AAA ATPase 1 gene MP:0012128 abnormal blastocyst formation IAGP N RGD:5509061 20160505 MGI PMID:22371176 68538 Ruvbl1 RuvB-like AAA ATPase 1 gene MP:0013776 bone marrow failure IAGP N RGD:5509061 20160505 MGI PMID:22371176 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:17950478 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:17950478 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20160804 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17950478 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20141003 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:17950478 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:17950478 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0000552 abnormal radius morphology IEA N RGD:5509061 20141003 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20141003 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17804598 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20141003 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:17804598 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0002705 dilated renal tubule IEA N RGD:5509061 20141003 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20141003 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17950478 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:17804598 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20160804 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:17804598 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:17804598 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0004447 small basioccipital bone IAGP N RGD:5509061 20141003 MGI PMID:17950478 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:17950478 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0005108 abnormal ulna morphology IEA N RGD:5509061 20141003 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0005358 abnormal incisor morphology IEA N RGD:5509061 20180201 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20160804 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160804 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20160804 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160804 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17804598 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:17804598 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20141003 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20141003 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160804 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:17804598 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17804598 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:17804598 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0010466 vascular ring IEA N RGD:5509061 20141003 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0010472 abnormal ascending aorta and coronary artery attachment IAGP N RGD:5509061 20141003 MGI PMID:17804598 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17804598 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17804598 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0011682 renal glomerulus cyst IEA N RGD:5509061 20141003 MGI 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0012747 abnormal cardiac neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17804598 68548 Ltbp1 latent transforming growth factor beta binding protein 1 gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20180125 MGI PMID:17950478 68550 Ltbp2 latent transforming growth factor beta binding protein 2 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20160505 MGI PMID:24908666 68550 Ltbp2 latent transforming growth factor beta binding protein 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10848613 68550 Ltbp2 latent transforming growth factor beta binding protein 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 68550 Ltbp2 latent transforming growth factor beta binding protein 2 gene MP:0014176 abnormal cilary zonule morphology IAGP N RGD:5509061 20160505 MGI PMID:24908666 68550 Ltbp2 latent transforming growth factor beta binding protein 2 gene MP:0031428 lens dislocation IAGP N RGD:5509061 20220714 MGI PMID:24908666 68551 Ddx25 DEAD box helicase 25 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15096601 68551 Ddx25 DEAD box helicase 25 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15096601 68551 Ddx25 DEAD box helicase 25 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15096601 68551 Ddx25 DEAD box helicase 25 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15096601 68551 Ddx25 DEAD box helicase 25 gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15096601 68551 Ddx25 DEAD box helicase 25 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15096601 68551 Ddx25 DEAD box helicase 25 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:15096601 68553 Cacnb1 calcium channel, voltage-dependent, beta 1 subunit gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:8943043 68553 Cacnb1 calcium channel, voltage-dependent, beta 1 subunit gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:8943043 68553 Cacnb1 calcium channel, voltage-dependent, beta 1 subunit gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:8943043 68553 Cacnb1 calcium channel, voltage-dependent, beta 1 subunit gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:8943043 68553 Cacnb1 calcium channel, voltage-dependent, beta 1 subunit gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:8943043 68553 Cacnb1 calcium channel, voltage-dependent, beta 1 subunit gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:8943043 68553 Cacnb1 calcium channel, voltage-dependent, beta 1 subunit gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:8943043 68553 Cacnb1 calcium channel, voltage-dependent, beta 1 subunit gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8943043 68553 Cacnb1 calcium channel, voltage-dependent, beta 1 subunit gene MP:0031495 absent prenatal movement IAGP N RGD:5509061 20230810 MGI PMID:8943043 68555 Ggcx gamma-glutamyl carboxylase gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20181004 MGI PMID:25753038 68555 Ggcx gamma-glutamyl carboxylase gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0001147 small testis IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0001577 anemia IAGP N RGD:5509061 20151001 MGI PMID:24520408 68555 Ggcx gamma-glutamyl carboxylase gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17327402 68555 Ggcx gamma-glutamyl carboxylase gene MP:0001925 male infertility IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0002083 premature death IAGP N RGD:5509061 20151001 MGI PMID:24520408 68555 Ggcx gamma-glutamyl carboxylase gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20181004 MGI PMID:25753038 68555 Ggcx gamma-glutamyl carboxylase gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0004898 uterine hemorrhage IAGP N RGD:5509061 20151001 MGI PMID:24520408 68555 Ggcx gamma-glutamyl carboxylase gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20181004 MGI PMID:25753038 68555 Ggcx gamma-glutamyl carboxylase gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20181004 MGI PMID:25753038 68555 Ggcx gamma-glutamyl carboxylase gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20151001 MGI PMID:24520408 68555 Ggcx gamma-glutamyl carboxylase gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20181004 MGI PMID:25753038 68555 Ggcx gamma-glutamyl carboxylase gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20151001 MGI PMID:24520408 68555 Ggcx gamma-glutamyl carboxylase gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20181004 MGI PMID:25753038 68555 Ggcx gamma-glutamyl carboxylase gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20181004 MGI PMID:25753038 68555 Ggcx gamma-glutamyl carboxylase gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17327402 68555 Ggcx gamma-glutamyl carboxylase gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17327402 68555 Ggcx gamma-glutamyl carboxylase gene MP:0011922 abnormal circulating osteocalcin level IAGP N RGD:5509061 20181004 MGI PMID:25753038 68555 Ggcx gamma-glutamyl carboxylase gene MP:0013138 thin body IAGP N RGD:5509061 20181004 MGI PMID:25753038 68555 Ggcx gamma-glutamyl carboxylase gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220120 MGI PMID:33526452 68555 Ggcx gamma-glutamyl carboxylase gene MP:0020215 impaired blood coagulation IAGP N RGD:5509061 20151001 MGI PMID:24520408 68555 Ggcx gamma-glutamyl carboxylase gene MP:0030985 decreased circulating osteocalcin level IAGP N RGD:5509061 20191219 MGI PMID:25753038 68555 Ggcx gamma-glutamyl carboxylase gene MP:0031137 vaginal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:24520408 68555 Ggcx gamma-glutamyl carboxylase gene MP:0031152 subcutaneous hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:24520408 68557 Ccnd1 cyclin D1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15315760 68557 Ccnd1 cyclin D1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:15315760 68557 Ccnd1 cyclin D1 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:7557388 68557 Ccnd1 cyclin D1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:7557388 68557 Ccnd1 cyclin D1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11134518 68557 Ccnd1 cyclin D1 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11134518 68557 Ccnd1 cyclin D1 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:11134518 68557 Ccnd1 cyclin D1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:12502747 68557 Ccnd1 cyclin D1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:16413468 68557 Ccnd1 cyclin D1 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:12502747 68557 Ccnd1 cyclin D1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12502747 68557 Ccnd1 cyclin D1 gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:11134518 68557 Ccnd1 cyclin D1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22037875 68557 Ccnd1 cyclin D1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11134518 68557 Ccnd1 cyclin D1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15657434 68557 Ccnd1 cyclin D1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12502747 68557 Ccnd1 cyclin D1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16099835 68557 Ccnd1 cyclin D1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7557388 68557 Ccnd1 cyclin D1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:16099835 68557 Ccnd1 cyclin D1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:10380928 68557 Ccnd1 cyclin D1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:16413468 68557 Ccnd1 cyclin D1 gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:11134518 68557 Ccnd1 cyclin D1 gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:7557388 68557 Ccnd1 cyclin D1 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:22037875 68557 Ccnd1 cyclin D1 gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:7557388 68557 Ccnd1 cyclin D1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12502747 68557 Ccnd1 cyclin D1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:12502747 68557 Ccnd1 cyclin D1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:10380928 68557 Ccnd1 cyclin D1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15657434 68557 Ccnd1 cyclin D1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16413468 68557 Ccnd1 cyclin D1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:7557388 68557 Ccnd1 cyclin D1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15315760 68557 Ccnd1 cyclin D1 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:19914164 68557 Ccnd1 cyclin D1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10380928 68557 Ccnd1 cyclin D1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15657434 68557 Ccnd1 cyclin D1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16413468 68557 Ccnd1 cyclin D1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20090754 68557 Ccnd1 cyclin D1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22037875 68557 Ccnd1 cyclin D1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11134518 68557 Ccnd1 cyclin D1 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:11134518 68557 Ccnd1 cyclin D1 gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11134518 68557 Ccnd1 cyclin D1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16099835 68557 Ccnd1 cyclin D1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12502747 68557 Ccnd1 cyclin D1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15315760 68557 Ccnd1 cyclin D1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17699765 68557 Ccnd1 cyclin D1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20090754 68557 Ccnd1 cyclin D1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23079655 68557 Ccnd1 cyclin D1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:15315760 68557 Ccnd1 cyclin D1 gene MP:0002296 aspiration IAGP N RGD:5509061 20141003 MGI PMID:12502747 68557 Ccnd1 cyclin D1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15315760 68557 Ccnd1 cyclin D1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12183406 68557 Ccnd1 cyclin D1 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:11134518 68557 Ccnd1 cyclin D1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15315760 68557 Ccnd1 cyclin D1 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10380928 68557 Ccnd1 cyclin D1 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12502747 68557 Ccnd1 cyclin D1 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15657434 68557 Ccnd1 cyclin D1 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16413468 68557 Ccnd1 cyclin D1 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7557388 68557 Ccnd1 cyclin D1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23079655 68557 Ccnd1 cyclin D1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:16099835 68557 Ccnd1 cyclin D1 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15315760 68557 Ccnd1 cyclin D1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:15315760 68557 Ccnd1 cyclin D1 gene MP:0004831 long incisors IAGP N RGD:5509061 20180125 MGI PMID:7557388 68557 Ccnd1 cyclin D1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10380928 68557 Ccnd1 cyclin D1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15657434 68557 Ccnd1 cyclin D1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16413468 68557 Ccnd1 cyclin D1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:10380928 68557 Ccnd1 cyclin D1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:15657434 68557 Ccnd1 cyclin D1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:7557388 68557 Ccnd1 cyclin D1 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:7557388 68557 Ccnd1 cyclin D1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15315760 68557 Ccnd1 cyclin D1 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:7557388 68557 Ccnd1 cyclin D1 gene MP:0008509 disorganized retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:7557388 68557 Ccnd1 cyclin D1 gene MP:0009718 absent Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:12502747 68557 Ccnd1 cyclin D1 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:12502747 68557 Ccnd1 cyclin D1 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22037875 68557 Ccnd1 cyclin D1 gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:22037875 68557 Ccnd1 cyclin D1 gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:7557388 68557 Ccnd1 cyclin D1 gene MP:0010249 lactation failure IAGP N RGD:5509061 20150409 MGI PMID:15657434 68557 Ccnd1 cyclin D1 gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16413468 68557 Ccnd1 cyclin D1 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22037875 68557 Ccnd1 cyclin D1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11134518 68557 Ccnd1 cyclin D1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16413468 68557 Ccnd1 cyclin D1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12502747 68557 Ccnd1 cyclin D1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15315760 68557 Ccnd1 cyclin D1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7557388 68557 Ccnd1 cyclin D1 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:12756179 68557 Ccnd1 cyclin D1 gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20180125 MGI PMID:7557388 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0000436 abnormal head movements IEA N RGD:5509061 20111116 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0000635 pituitary gland hyperplasia IEA N RGD:5509061 20111116 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:5037658 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:5037658 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:5037658 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17320843 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0000947 convulsive seizures IEA N RGD:5509061 20111116 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:17320843 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001134 absent corpus luteum IEA N RGD:5509061 20111116 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20111215 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12223573 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:12223573 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12223573 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12223573 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:12223573 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:12223573 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001524 impaired limb coordination IEA N RGD:5509061 20111116 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001732 postnatal growth retardation IEA N RGD:5509061 20111116 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20150326 MGI PMID:5037658 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001921 reduced fertility IEA N RGD:5509061 20111116 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:1321503 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0002065 abnormal fear/anxiety-related behavior IEA N RGD:5509061 20111116 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12223573 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12151514 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:5037658 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:5037658 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:12223573 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0003313 abnormal locomotor activation IEA N RGD:5509061 20111116 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:12223573 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:13525 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0004924 abnormal behavior IEA N RGD:5509061 20111116 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:12223573 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:1321503 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:5037658 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:5037658 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17028169 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:5037658 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0005202 lethargy IEA N RGD:5509061 20111116 MGI 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:7261997 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17028169 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16636205 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:5037658 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:5037658 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:410895 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17028169 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:17028169 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17028169 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:7261997 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:1321503 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0013741 absent thymus corticomedullary boundary IAGP N RGD:5509061 20150430 MGI PMID:5037658 68559 Cacnb4 calcium channel, voltage-dependent, beta 4 subunit gene MP:0030143 facial muscle spasm IAGP N RGD:5509061 20171005 MGI PMID:12223573 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:11683991 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:11683991 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:11683991 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11683991 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20463662 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11683991 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11683991 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:20463662 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20463662 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:11683991 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20463662 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20463662 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:20463662 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:20463662 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:20463662 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20463662 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:20463662 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:20463662 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:20463662 68561 Inpp4a inositol polyphosphate-4-phosphatase, type I gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11683991 68563 Slc7a2 solute carrier family 7 (cationic amino acid transporter, y+ system), member 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:11278602 68563 Slc7a2 solute carrier family 7 (cationic amino acid transporter, y+ system), member 2 gene MP:0004357 long tibia IEA N RGD:5509061 20210128 MGI 68563 Slc7a2 solute carrier family 7 (cationic amino acid transporter, y+ system), member 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20221215 MGI 68563 Slc7a2 solute carrier family 7 (cationic amino acid transporter, y+ system), member 2 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 68563 Slc7a2 solute carrier family 7 (cationic amino acid transporter, y+ system), member 2 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 68563 Slc7a2 solute carrier family 7 (cationic amino acid transporter, y+ system), member 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 68565 Nmu neuromedin U gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:19070594 68565 Nmu neuromedin U gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:15448684 68565 Nmu neuromedin U gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:15448684 68567 Epha3 Eph receptor A3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 68567 Epha3 Eph receptor A3 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 68567 Epha3 Eph receptor A3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 68567 Epha3 Eph receptor A3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 68567 Epha3 Eph receptor A3 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 68567 Epha3 Eph receptor A3 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0001258 decreased body length IEA N RGD:5509061 20210826 MGI 68567 Epha3 Eph receptor A3 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20231207 MGI 68567 Epha3 Eph receptor A3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 68567 Epha3 Eph receptor A3 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 68567 Epha3 Eph receptor A3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 68567 Epha3 Eph receptor A3 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0003402 decreased liver weight IEA N RGD:5509061 20220519 MGI 68567 Epha3 Eph receptor A3 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:14585969 68567 Epha3 Eph receptor A3 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 68567 Epha3 Eph receptor A3 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0006046 atrioventricular valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0006137 venoocclusion IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:14585969 68567 Epha3 Eph receptor A3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0010592 abnormal atrioventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0010909 pulmonary alveolar hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14585969 68567 Epha3 Eph receptor A3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17046737 68567 Epha3 Eph receptor A3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 68567 Epha3 Eph receptor A3 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20191128 MGI PMID:17046737 68571 Pde7a phosphodiesterase 7A gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:14662840 68573 Alas1 aminolevulinic acid synthase 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20221215 MGI 68573 Alas1 aminolevulinic acid synthase 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 68573 Alas1 aminolevulinic acid synthase 1 gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 68573 Alas1 aminolevulinic acid synthase 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 68573 Alas1 aminolevulinic acid synthase 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 68573 Alas1 aminolevulinic acid synthase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20015225 68573 Alas1 aminolevulinic acid synthase 1 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20221215 MGI 68573 Alas1 aminolevulinic acid synthase 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20015225 68573 Alas1 aminolevulinic acid synthase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 68573 Alas1 aminolevulinic acid synthase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 68575 Kcnd2 potassium voltage-gated channel, Shal-related family, member 2 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:16600858 68575 Kcnd2 potassium voltage-gated channel, Shal-related family, member 2 gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:16600858 68575 Kcnd2 potassium voltage-gated channel, Shal-related family, member 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16600858 68575 Kcnd2 potassium voltage-gated channel, Shal-related family, member 2 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:16293790 68575 Kcnd2 potassium voltage-gated channel, Shal-related family, member 2 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:16600858 68575 Kcnd2 potassium voltage-gated channel, Shal-related family, member 2 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:16600858 68577 Kcnd3 potassium voltage-gated channel, Shal-related family, member 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 68577 Kcnd3 potassium voltage-gated channel, Shal-related family, member 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 68577 Kcnd3 potassium voltage-gated channel, Shal-related family, member 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 68577 Kcnd3 potassium voltage-gated channel, Shal-related family, member 3 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20181227 MGI 68577 Kcnd3 potassium voltage-gated channel, Shal-related family, member 3 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 68577 Kcnd3 potassium voltage-gated channel, Shal-related family, member 3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230601 MGI 68577 Kcnd3 potassium voltage-gated channel, Shal-related family, member 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 68579 Hsf2 heat shock factor 2 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:12748967 68579 Hsf2 heat shock factor 2 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:12748967 68579 Hsf2 heat shock factor 2 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12748967 68579 Hsf2 heat shock factor 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12748967 68579 Hsf2 heat shock factor 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12748967 68579 Hsf2 heat shock factor 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12748967 68579 Hsf2 heat shock factor 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12748967 68579 Hsf2 heat shock factor 2 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12391166 68579 Hsf2 heat shock factor 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12748967 68579 Hsf2 heat shock factor 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0003870 decreased urine glucose level IEA N RGD:5509061 20240523 MGI 68579 Hsf2 heat shock factor 2 gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20170105 MGI 68579 Hsf2 heat shock factor 2 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 68579 Hsf2 heat shock factor 2 gene MP:0006361 abnormal female germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:12032072 68579 Hsf2 heat shock factor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12748967 68579 Hsf2 heat shock factor 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12748967 68579 Hsf2 heat shock factor 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14994269 68579 Hsf2 heat shock factor 2 gene MP:0012681 collapsed brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:12748967 68579 Hsf2 heat shock factor 2 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:14994269 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11343120 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:15654325 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:15654325 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11343120 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15654325 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11343120 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11343120 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11343120 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15654325 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15654325 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15654325 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11343120 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11343120 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:11343120 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15654325 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:11343120 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11343120 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11343120 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15654325 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15654325 68581 Inppl1 inositol polyphosphate phosphatase-like 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11343120 68583 Syt4 synaptotagmin IV gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 68583 Syt4 synaptotagmin IV gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10792055 68583 Syt4 synaptotagmin IV gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 68583 Syt4 synaptotagmin IV gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:10792055 68583 Syt4 synaptotagmin IV gene MP:0002969 impaired social transmission of food preference IAGP N RGD:5509061 20141003 MGI PMID:10792055 68583 Syt4 synaptotagmin IV gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20200514 MGI 68583 Syt4 synaptotagmin IV gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 68583 Syt4 synaptotagmin IV gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20200514 MGI 68585 Kcnh1 potassium voltage-gated channel, subfamily H (eag-related), member 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23424202 68585 Kcnh1 potassium voltage-gated channel, subfamily H (eag-related), member 1 gene MP:0003360 abnormal depression-related behavior IEA N RGD:5509061 20141003 MGI 68585 Kcnh1 potassium voltage-gated channel, subfamily H (eag-related), member 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:23424202 68586 Syt8 synaptotagmin VIII gene MP:0001513 limb grasping IEA N RGD:5509061 20220519 MGI 68586 Syt8 synaptotagmin VIII gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20240523 MGI 68586 Syt8 synaptotagmin VIII gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 68591 Dpp6 dipeptidylpeptidase 6 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21943606 68591 Dpp6 dipeptidylpeptidase 6 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20141003 MGI PMID:21943606 68591 Dpp6 dipeptidylpeptidase 6 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:21943606 68591 Dpp6 dipeptidylpeptidase 6 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:21943606 68593 Dbt dihydrolipoamide branched chain transacylase E2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16579849 68593 Dbt dihydrolipoamide branched chain transacylase E2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16579849 68593 Dbt dihydrolipoamide branched chain transacylase E2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16579849 68593 Dbt dihydrolipoamide branched chain transacylase E2 gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:16579849 68593 Dbt dihydrolipoamide branched chain transacylase E2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16579849 68593 Dbt dihydrolipoamide branched chain transacylase E2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:16579849 68593 Dbt dihydrolipoamide branched chain transacylase E2 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:16579849 68593 Dbt dihydrolipoamide branched chain transacylase E2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16579849 68593 Dbt dihydrolipoamide branched chain transacylase E2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16579849 68593 Dbt dihydrolipoamide branched chain transacylase E2 gene MP:0030674 decreased circulating alanine level IAGP N RGD:5509061 20180927 MGI PMID:16579849 68593 Dbt dihydrolipoamide branched chain transacylase E2 gene MP:0030710 decreased circulating glutamine level IAGP N RGD:5509061 20180927 MGI PMID:16579849 68593 Dbt dihydrolipoamide branched chain transacylase E2 gene MP:0030740 decreased circulating glutamic acid level IAGP N RGD:5509061 20180927 MGI PMID:16579849 68595 Epas1 endothelial PAS domain protein 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20170209 MGI PMID:17284606 68595 Epas1 endothelial PAS domain protein 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20170209 MGI PMID:21419768 68595 Epas1 endothelial PAS domain protein 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20170209 MGI PMID:23264599 68595 Epas1 endothelial PAS domain protein 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20210729 MGI PMID:31848220 68595 Epas1 endothelial PAS domain protein 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:23640890 68595 Epas1 endothelial PAS domain protein 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:23640890 68595 Epas1 endothelial PAS domain protein 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20170209 MGI PMID:10880563 68595 Epas1 endothelial PAS domain protein 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20170209 MGI PMID:12053176 68595 Epas1 endothelial PAS domain protein 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170209 MGI 68595 Epas1 endothelial PAS domain protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170209 MGI PMID:17284606 68595 Epas1 endothelial PAS domain protein 1 gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20170209 MGI PMID:18332118 68595 Epas1 endothelial PAS domain protein 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20170209 MGI PMID:12053176 68595 Epas1 endothelial PAS domain protein 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20170209 MGI PMID:12053176 68595 Epas1 endothelial PAS domain protein 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20170209 MGI PMID:12053176 68595 Epas1 endothelial PAS domain protein 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20170209 MGI PMID:12750401 68595 Epas1 endothelial PAS domain protein 1 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20170209 MGI PMID:17284606 68595 Epas1 endothelial PAS domain protein 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20170209 MGI PMID:12053176 68595 Epas1 endothelial PAS domain protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20170209 MGI PMID:17284606 68595 Epas1 endothelial PAS domain protein 1 gene MP:0001577 anemia IAGP N RGD:5509061 20210729 MGI PMID:31848220 68595 Epas1 endothelial PAS domain protein 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20170209 MGI PMID:10880563 68595 Epas1 endothelial PAS domain protein 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20170209 MGI PMID:12053176 68595 Epas1 endothelial PAS domain protein 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20170209 MGI PMID:12053176 68595 Epas1 endothelial PAS domain protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20170209 MGI PMID:24121508 68595 Epas1 endothelial PAS domain protein 1 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20170209 MGI PMID:12053176 68595 Epas1 endothelial PAS domain protein 1 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20170209 MGI PMID:17284606 68595 Epas1 endothelial PAS domain protein 1 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20170209 MGI PMID:23640890 68595 Epas1 endothelial PAS domain protein 1 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20210729 MGI PMID:31848220 68595 Epas1 endothelial PAS domain protein 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20170209 MGI PMID:23640890 68595 Epas1 endothelial PAS domain protein 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20170209 MGI PMID:17284606 68595 Epas1 endothelial PAS domain protein 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20170209 MGI PMID:21419768 68595 Epas1 endothelial PAS domain protein 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20170209 MGI PMID:23264599 68595 Epas1 endothelial PAS domain protein 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:17284606 68595 Epas1 endothelial PAS domain protein 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:21419768 68595 Epas1 endothelial PAS domain protein 1 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20170209 MGI PMID:23640890 68595 Epas1 endothelial PAS domain protein 1 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:23640890 68595 Epas1 endothelial PAS domain protein 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20170209 MGI PMID:10880563 68595 Epas1 endothelial PAS domain protein 1 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20170209 MGI PMID:12606578 68595 Epas1 endothelial PAS domain protein 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20170209 MGI PMID:12606578 68595 Epas1 endothelial PAS domain protein 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20170209 MGI PMID:12053176 68595 Epas1 endothelial PAS domain protein 1 gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20170209 MGI PMID:21419768 68595 Epas1 endothelial PAS domain protein 1 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20170209 MGI PMID:12053176 68595 Epas1 endothelial PAS domain protein 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20170209 MGI PMID:18332118 68595 Epas1 endothelial PAS domain protein 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20170209 MGI PMID:23640890 68595 Epas1 endothelial PAS domain protein 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20170209 MGI PMID:23640890 68595 Epas1 endothelial PAS domain protein 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20170209 MGI PMID:12750401 68595 Epas1 endothelial PAS domain protein 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20170209 MGI PMID:9808618 68595 Epas1 endothelial PAS domain protein 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20170209 MGI PMID:12606578 68595 Epas1 endothelial PAS domain protein 1 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20170209 MGI PMID:23640890 68595 Epas1 endothelial PAS domain protein 1 gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20170209 MGI PMID:23640890 68595 Epas1 endothelial PAS domain protein 1 gene MP:0005664 decreased circulating noradrenaline level IAGP N RGD:5509061 20170209 MGI PMID:9808618 68595 Epas1 endothelial PAS domain protein 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20170209 MGI PMID:9808618 68595 Epas1 endothelial PAS domain protein 1 gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20170209 MGI PMID:17284606 68595 Epas1 endothelial PAS domain protein 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20170209 MGI PMID:22464323 68595 Epas1 endothelial PAS domain protein 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20170209 MGI PMID:10880563 68595 Epas1 endothelial PAS domain protein 1 gene MP:0010017 visceral vascular congestion IAGP N RGD:5509061 20170209 MGI PMID:9808618 68595 Epas1 endothelial PAS domain protein 1 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20170209 MGI PMID:9808618 68595 Epas1 endothelial PAS domain protein 1 gene MP:0010021 heart vascular congestion IAGP N RGD:5509061 20170209 MGI PMID:9808618 68595 Epas1 endothelial PAS domain protein 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240627 MGI 68595 Epas1 endothelial PAS domain protein 1 gene MP:0010460 pulmonary artery hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:23640890 68595 Epas1 endothelial PAS domain protein 1 gene MP:0010755 abnormal heart right ventricle pressure IAGP N RGD:5509061 20170209 MGI PMID:23640890 68595 Epas1 endothelial PAS domain protein 1 gene MP:0010811 decreased type II pneumocyte number IAGP N RGD:5509061 20170209 MGI PMID:12053176 68595 Epas1 endothelial PAS domain protein 1 gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20170209 MGI PMID:12053176 68595 Epas1 endothelial PAS domain protein 1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:23640890 68595 Epas1 endothelial PAS domain protein 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20170209 MGI PMID:22464323 68595 Epas1 endothelial PAS domain protein 1 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20170209 MGI PMID:22464323 68595 Epas1 endothelial PAS domain protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:10880563 68595 Epas1 endothelial PAS domain protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:12053176 68595 Epas1 endothelial PAS domain protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:12750401 68595 Epas1 endothelial PAS domain protein 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:17284606 68595 Epas1 endothelial PAS domain protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:10880563 68595 Epas1 endothelial PAS domain protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:9808618 68595 Epas1 endothelial PAS domain protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 68595 Epas1 endothelial PAS domain protein 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:12750401 68595 Epas1 endothelial PAS domain protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:10880563 68595 Epas1 endothelial PAS domain protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:12053176 68595 Epas1 endothelial PAS domain protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20170209 MGI PMID:9808618 68595 Epas1 endothelial PAS domain protein 1 gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20170209 MGI PMID:23640890 68595 Epas1 endothelial PAS domain protein 1 gene MP:0011286 decreased circulating erythropoietin level IAGP N RGD:5509061 20170209 MGI PMID:22464323 68595 Epas1 endothelial PAS domain protein 1 gene MP:0020843 abnormal type I cell of carotid body physiology IAGP N RGD:5509061 20210729 MGI PMID:31848220 68595 Epas1 endothelial PAS domain protein 1 gene MP:0031252 abnormal physiological response to hypoxia IAGP N RGD:5509061 20210729 MGI PMID:31848220 68598 Timm22 translocase of inner mitochondrial membrane 22 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 68598 Timm22 translocase of inner mitochondrial membrane 22 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191128 MGI 68598 Timm22 translocase of inner mitochondrial membrane 22 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20241024 MGI PMID:32376682 68598 Timm22 translocase of inner mitochondrial membrane 22 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191128 MGI 68598 Timm22 translocase of inner mitochondrial membrane 22 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 68598 Timm22 translocase of inner mitochondrial membrane 22 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191128 MGI 68598 Timm22 translocase of inner mitochondrial membrane 22 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 68598 Timm22 translocase of inner mitochondrial membrane 22 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191128 MGI 68598 Timm22 translocase of inner mitochondrial membrane 22 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 68598 Timm22 translocase of inner mitochondrial membrane 22 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 68598 Timm22 translocase of inner mitochondrial membrane 22 gene MP:0012724 absent head fold IEA N RGD:5509061 20191128 MGI 68598 Timm22 translocase of inner mitochondrial membrane 22 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191128 MGI 68598 Timm22 translocase of inner mitochondrial membrane 22 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22555591 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:12475886 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000276 heart right ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000585 kinked tail IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:22555591 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15314648 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:15314648 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:22555591 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000821 choroid plexus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15314648 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:22555591 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15314648 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20653565 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001123 dilated uterus IAGP N RGD:5509061 20141003 MGI PMID:16143106 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:16143106 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:22555591 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001296 macrophthalmia IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20653565 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001775 abnormal selenium level IAGP N RGD:5509061 20141003 MGI PMID:20653565 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001775 abnormal selenium level IAGP N RGD:5509061 20151210 MGI PMID:24434121 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:17846082 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:22555591 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:20798259 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:22555591 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002625 heart left ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002639 micrognathia IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002698 abnormal sclera morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:22555591 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:16143106 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:20798259 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:12475886 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:12475886 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:10514418 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:12475886 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:20531455 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:20653565 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:12475886 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0003052 omphalocele IEA N RGD:5509061 20141009 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0003101 high myopia IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0003102 sclera thinning IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0003509 increased circulating dihydrotestosterone level IAGP N RGD:5509061 20141003 MGI PMID:16143106 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:16143106 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0003675 kidney cyst IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:16143106 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0003878 abnormal ear physiology IAGP N RGD:5509061 20141003 MGI PMID:17846082 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0004056 abnormal myocardium compact layer morphology IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0004113 abnormal aortic arch morphology IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0004158 right aortic arch IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0004366 abnormal strial marginal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17846082 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:17846082 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10514418 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20141003 MGI PMID:22555591 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:12475886 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:20531455 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:22555591 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0005195 abnormal posterior eye segment morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0005257 abnormal intraocular pressure IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0006241 abnormal placement of pupils IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:17846082 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0006357 abnormal circulating mineral level IAGP N RGD:5509061 20141003 MGI PMID:20653565 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20141003 MGI PMID:22555591 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0009445 osteomalacia IAGP N RGD:5509061 20141003 MGI PMID:12475886 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10514418 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12475886 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0009708 vaginal septum IAGP N RGD:5509061 20141003 MGI PMID:16143106 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:20798259 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:12475886 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0010146 umbilical hernia IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0010466 vascular ring IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20798259 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17846082 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20531455 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:12475886 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0011555 increased urine microglobulin level IAGP N RGD:5509061 20141003 MGI PMID:10514418 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0011603 decreased glutathione peroxidase activity IAGP N RGD:5509061 20141003 MGI PMID:20653565 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0011603 decreased glutathione peroxidase activity IAGP N RGD:5509061 20151210 MGI PMID:24434121 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0011661 persistent truncus arteriosus type i IEA N RGD:5509061 20141003 MGI 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0011770 increased urine selenium level IAGP N RGD:5509061 20141003 MGI PMID:20653565 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0011770 increased urine selenium level IAGP N RGD:5509061 20151210 MGI PMID:24434121 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17846082 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20181011 MGI PMID:26107939 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0030046 round forehead IAGP N RGD:5509061 20170921 MGI PMID:22555591 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0030047 flat forehead IAGP N RGD:5509061 20170921 MGI PMID:8710893 68600 Lrp2 low density lipoprotein receptor-related protein 2 gene MP:0031286 unilateral cryptorchism IAGP N RGD:5509061 20211014 MGI PMID:16143106 68602 Lasp1 LIM and SH3 protein 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:12438746 68602 Lasp1 LIM and SH3 protein 1 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:18483181 68602 Lasp1 LIM and SH3 protein 1 gene MP:0000503 excessive digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:18483181 68602 Lasp1 LIM and SH3 protein 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:18483181 68602 Lasp1 LIM and SH3 protein 1 gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:18483181 68602 Lasp1 LIM and SH3 protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18483181 68602 Lasp1 LIM and SH3 protein 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0003639 abnormal response to vitamins IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0004606 absent vertebral spinous process IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0004626 vertebral compression IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0004706 short vertebral body IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0005226 abnormal vertebral arch development IAGP N RGD:5509061 20141003 MGI PMID:12438746 68602 Lasp1 LIM and SH3 protein 1 gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0006394 abnormal vertebral epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19378260 68602 Lasp1 LIM and SH3 protein 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19378260 68604 Aldh9a1 aldehyde dehydrogenase 9, subfamily A1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20190502 MGI 68604 Aldh9a1 aldehyde dehydrogenase 9, subfamily A1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:23938297 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20230601 MGI 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0000322 increased granulocyte number IEA N RGD:5509061 20230601 MGI 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:23938297 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:17941048 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23938297 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17941048 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20141003 MGI PMID:17941048 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:23938297 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0003959 abnormal lean body mass IEA N RGD:5509061 20240523 MGI 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0005103 abnormal retina pigmentation IEA N RGD:5509061 20111116 MGI 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:23938297 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0005333 decreased heart rate IEA N RGD:5509061 20240523 MGI 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:17941048 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:17941048 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0009891 abnormal palate bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230601 MGI 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15361870 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0011951 increased cardiac stroke volume IEA N RGD:5509061 20240523 MGI 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0013886 increased CD4-negative, CD25-positive NK T cell number IEA N RGD:5509061 20240523 MGI 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0014079 decreased small intestinal villus number IAGP N RGD:5509061 20160414 MGI PMID:23938297 68606 Pdgfc platelet-derived growth factor, C polypeptide gene MP:0030203 short nasal septum IAGP N RGD:5509061 20171012 MGI PMID:15361870 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12070287 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20458146 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20458146 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20458146 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12070287 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20458146 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:15705783 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:20458146 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12070287 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12070287 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20458146 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15705783 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12070287 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15705783 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12070287 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:15705783 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16332975 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20458146 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12070287 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20458146 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:12070287 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:20458146 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:12070287 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0008112 abnormal monocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:12070287 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12070287 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20458146 68608 Sh2b3 SH2B adaptor protein 3 gene MP:0011746 spleen fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12070287 68610 Pkn1 protein kinase N1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20160421 MGI 68610 Pkn1 protein kinase N1 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20181227 MGI 68610 Pkn1 protein kinase N1 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20181227 MGI 68610 Pkn1 protein kinase N1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20190314 MGI PMID:29045568 68610 Pkn1 protein kinase N1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20171109 MGI PMID:26774483 68610 Pkn1 protein kinase N1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23223530 68610 Pkn1 protein kinase N1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:23223530 68610 Pkn1 protein kinase N1 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20190314 MGI PMID:29045568 68610 Pkn1 protein kinase N1 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20190314 MGI PMID:29045568 68610 Pkn1 protein kinase N1 gene MP:0003824 decreased left ventricle developed pressure IAGP N RGD:5509061 20190314 MGI PMID:29045568 68610 Pkn1 protein kinase N1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20190314 MGI PMID:29045568 68610 Pkn1 protein kinase N1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:23223530 68610 Pkn1 protein kinase N1 gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:23223530 68610 Pkn1 protein kinase N1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 68610 Pkn1 protein kinase N1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20190314 MGI PMID:29045568 68610 Pkn1 protein kinase N1 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23223530 68610 Pkn1 protein kinase N1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20201022 MGI 68610 Pkn1 protein kinase N1 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:23223530 68610 Pkn1 protein kinase N1 gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23223530 68610 Pkn1 protein kinase N1 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:23223530 68610 Pkn1 protein kinase N1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:23223530 68610 Pkn1 protein kinase N1 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:23223530 68610 Pkn1 protein kinase N1 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:23223530 68610 Pkn1 protein kinase N1 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:23223530 68610 Pkn1 protein kinase N1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20160421 MGI 68610 Pkn1 protein kinase N1 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 68610 Pkn1 protein kinase N1 gene MP:0010675 decreased activation-induced B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23223530 68610 Pkn1 protein kinase N1 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:23223530 68610 Pkn1 protein kinase N1 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:23223530 68610 Pkn1 protein kinase N1 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20190314 MGI PMID:29045568 68610 Pkn1 protein kinase N1 gene MP:0012361 decreased large unstained cell number IEA N RGD:5509061 20181227 MGI 68610 Pkn1 protein kinase N1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 68610 Pkn1 protein kinase N1 gene MP:0020419 decreased cardiac muscle relaxation IAGP N RGD:5509061 20190314 MGI PMID:29045568 68610 Pkn1 protein kinase N1 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:23223530 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21921034 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21921034 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0001258 decreased body length IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21921034 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21921034 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160804 MGI 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21921034 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0003345 decreased rib number IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:21921034 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160804 MGI 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:17376776 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0004614 caudal vertebral transformation IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0004648 decreased thoracic vertebrae number IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0004677 truncated ribs IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0005015 increased T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160804 MGI 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20160922 MGI PMID:24652767 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21921034 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:21921034 68615 Ppp5c protein phosphatase 5, catalytic subunit gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160922 MGI PMID:24652767 68617 Dlc1 deleted in liver cancer 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15710412 68617 Dlc1 deleted in liver cancer 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:20199662 68617 Dlc1 deleted in liver cancer 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:20199662 68617 Dlc1 deleted in liver cancer 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:15710412 68617 Dlc1 deleted in liver cancer 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:15710412 68617 Dlc1 deleted in liver cancer 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:20199662 68617 Dlc1 deleted in liver cancer 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:20199662 68617 Dlc1 deleted in liver cancer 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:20199662 68617 Dlc1 deleted in liver cancer 1 gene MP:0001889 delayed brain development IAGP N RGD:5509061 20141003 MGI PMID:20199662 68617 Dlc1 deleted in liver cancer 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20199662 68617 Dlc1 deleted in liver cancer 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15710412 68617 Dlc1 deleted in liver cancer 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23010077 68617 Dlc1 deleted in liver cancer 1 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20199662 68617 Dlc1 deleted in liver cancer 1 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:20199662 68617 Dlc1 deleted in liver cancer 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15710412 68617 Dlc1 deleted in liver cancer 1 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:20199662 68617 Dlc1 deleted in liver cancer 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20199662 68617 Dlc1 deleted in liver cancer 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:15710412 68617 Dlc1 deleted in liver cancer 1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:15710412 68617 Dlc1 deleted in liver cancer 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20199662 68617 Dlc1 deleted in liver cancer 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23010077 68617 Dlc1 deleted in liver cancer 1 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:15710412 68617 Dlc1 deleted in liver cancer 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15710412 68617 Dlc1 deleted in liver cancer 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20199662 68617 Dlc1 deleted in liver cancer 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20199662 68617 Dlc1 deleted in liver cancer 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15710412 68617 Dlc1 deleted in liver cancer 1 gene MP:0011709 increased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:20199662 68617 Dlc1 deleted in liver cancer 1 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:20199662 68619 Ncs1 neuronal calcium sensor 1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20170105 MGI 68619 Ncs1 neuronal calcium sensor 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210826 MGI 68619 Ncs1 neuronal calcium sensor 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 68619 Ncs1 neuronal calcium sensor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 68619 Ncs1 neuronal calcium sensor 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 68620 Dio2 deiodinase, iodothyronine, type II gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23524969 68620 Dio2 deiodinase, iodothyronine, type II gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11731615 68620 Dio2 deiodinase, iodothyronine, type II gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11731615 68620 Dio2 deiodinase, iodothyronine, type II gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:16223863 68620 Dio2 deiodinase, iodothyronine, type II gene MP:0003971 abnormal thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11731615 68620 Dio2 deiodinase, iodothyronine, type II gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11731615 68620 Dio2 deiodinase, iodothyronine, type II gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:23524969 68620 Dio2 deiodinase, iodothyronine, type II gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:23524969 68620 Dio2 deiodinase, iodothyronine, type II gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20171228 MGI PMID:11696583 68620 Dio2 deiodinase, iodothyronine, type II gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:11731615 68620 Dio2 deiodinase, iodothyronine, type II gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:23524969 68620 Dio2 deiodinase, iodothyronine, type II gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16223863 68620 Dio2 deiodinase, iodothyronine, type II gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23524969 68620 Dio2 deiodinase, iodothyronine, type II gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20171228 MGI PMID:11696583 68622 Pfkm phosphofructokinase, muscle gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 68622 Pfkm phosphofructokinase, muscle gene MP:0000601 small liver IEA N RGD:5509061 20210826 MGI 68622 Pfkm phosphofructokinase, muscle gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220519 MGI 68622 Pfkm phosphofructokinase, muscle gene MP:0001148 enlarged testis IEA N RGD:5509061 20220519 MGI 68622 Pfkm phosphofructokinase, muscle gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20220519 MGI 68622 Pfkm phosphofructokinase, muscle gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 68622 Pfkm phosphofructokinase, muscle gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 68622 Pfkm phosphofructokinase, muscle gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 68622 Pfkm phosphofructokinase, muscle gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 68622 Pfkm phosphofructokinase, muscle gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17595219 68622 Pfkm phosphofructokinase, muscle gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 68622 Pfkm phosphofructokinase, muscle gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17595219 68622 Pfkm phosphofructokinase, muscle gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0002944 increased lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17595219 68622 Pfkm phosphofructokinase, muscle gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220519 MGI 68622 Pfkm phosphofructokinase, muscle gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17595219 68622 Pfkm phosphofructokinase, muscle gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17595219 68622 Pfkm phosphofructokinase, muscle gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 68622 Pfkm phosphofructokinase, muscle gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20160310 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:19696889 68622 Pfkm phosphofructokinase, muscle gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:19696889 68624 Dio3 deiodinase, iodothyronine type III gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16410833 68624 Dio3 deiodinase, iodothyronine type III gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16410833 68624 Dio3 deiodinase, iodothyronine type III gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:12399446 68624 Dio3 deiodinase, iodothyronine type III gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20160602 MGI PMID:25004090 68624 Dio3 deiodinase, iodothyronine type III gene MP:0003965 abnormal pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:16410833 68624 Dio3 deiodinase, iodothyronine type III gene MP:0005119 decreased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:16410833 68624 Dio3 deiodinase, iodothyronine type III gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:16410833 68624 Dio3 deiodinase, iodothyronine type III gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20160602 MGI PMID:25004090 68624 Dio3 deiodinase, iodothyronine type III gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:16410833 68624 Dio3 deiodinase, iodothyronine type III gene MP:0005474 increased triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:16410833 68624 Dio3 deiodinase, iodothyronine type III gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20160602 MGI PMID:25004090 68624 Dio3 deiodinase, iodothyronine type III gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:16410833 68624 Dio3 deiodinase, iodothyronine type III gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:16410833 68624 Dio3 deiodinase, iodothyronine type III gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20160602 MGI PMID:25004090 68624 Dio3 deiodinase, iodothyronine type III gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16410833 68624 Dio3 deiodinase, iodothyronine type III gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16410833 68627 Cldn1 claudin 1 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:11889141 68627 Cldn1 claudin 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:11889141 68627 Cldn1 claudin 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:11889141 68627 Cldn1 claudin 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11889141 68627 Cldn1 claudin 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 68627 Cldn1 claudin 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:11889141 68627 Cldn1 claudin 1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:11889141 68627 Cldn1 claudin 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:11889141 68627 Cldn1 claudin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11889141 68627 Cldn1 claudin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170105 MGI 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20170309 MGI PMID:27466188 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17344405 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20170309 MGI PMID:27466188 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20170309 MGI PMID:27466188 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17344405 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20111116 MGI 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:17344405 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0003989 abnormal barrel cortex morphology IAGP N RGD:5509061 20170309 MGI PMID:27466188 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0004073 caudal body truncation IEA N RGD:5509061 20141003 MGI 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0004180 failure of initiation of embryo turning IEA N RGD:5509061 20111116 MGI 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20170309 MGI PMID:27466188 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20170309 MGI PMID:27466188 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17344405 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17344405 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20170309 MGI PMID:27466188 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0011273 prolonged excitatory postsynaptic current decay time IAGP N RGD:5509061 20170309 MGI PMID:27466188 68629 Dlg3 discs large MAGUK scaffold protein 3 gene MP:0020066 abnormal neocortex size IAGP N RGD:5509061 20170309 MGI PMID:27466188 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0000745 tremors IEA N RGD:5509061 20181227 MGI 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16677619 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9853749 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:20952458 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20952458 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20150827 MGI PMID:20952458 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:14980210 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20952458 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20952458 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:20952458 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12427827 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:9853749 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:20952458 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:20952458 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:12593798 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:20952458 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:17148601 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:9853749 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:20467438 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:14980210 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0002802 abnormal discrimination learning IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17148601 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:17148601 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17148601 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:9853749 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12427827 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:14980210 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17148601 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:9853749 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0003177 allodynia IAGP N RGD:5509061 20141003 MGI PMID:12593798 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0003908 decreased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:16677619 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20181227 MGI 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:14980210 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:14980210 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:20952458 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16677619 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0010052 increased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20952458 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20181227 MGI 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0010166 increased response to stress-induced hyperthermia IAGP N RGD:5509061 20141003 MGI PMID:20952458 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9853749 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17344405 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17344405 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:23268962 68631 Dlg4 discs large MAGUK scaffold protein 4 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:20952458 68633 Cldn3 claudin 3 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20200514 MGI 68633 Cldn3 claudin 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 68635 Stx5a syntaxin 5A gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20200402 MGI 68635 Stx5a syntaxin 5A gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 68635 Stx5a syntaxin 5A gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20200402 MGI 68635 Stx5a syntaxin 5A gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20200402 MGI 68635 Stx5a syntaxin 5A gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20200402 MGI 68635 Stx5a syntaxin 5A gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20221215 MGI 68635 Stx5a syntaxin 5A gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20200402 MGI 68635 Stx5a syntaxin 5A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 68635 Stx5a syntaxin 5A gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 68639 Aqp3 aquaporin 3 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 68639 Aqp3 aquaporin 3 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:10737773 68639 Aqp3 aquaporin 3 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 68639 Aqp3 aquaporin 3 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:10737773 68639 Aqp3 aquaporin 3 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11382807 68639 Aqp3 aquaporin 3 gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IEA N RGD:5509061 20111116 MGI 68639 Aqp3 aquaporin 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10737773 68639 Aqp3 aquaporin 3 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 68639 Aqp3 aquaporin 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 68639 Aqp3 aquaporin 3 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:10737773 68639 Aqp3 aquaporin 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 68639 Aqp3 aquaporin 3 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 68639 Aqp3 aquaporin 3 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 68639 Aqp3 aquaporin 3 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 68639 Aqp3 aquaporin 3 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 68639 Aqp3 aquaporin 3 gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20111116 MGI 68639 Aqp3 aquaporin 3 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11382807 68639 Aqp3 aquaporin 3 gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:10737773 68639 Aqp3 aquaporin 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IEA N RGD:5509061 20111116 MGI 68639 Aqp3 aquaporin 3 gene MP:0010180 increased susceptibility to weight loss IEA N RGD:5509061 20111116 MGI 68639 Aqp3 aquaporin 3 gene MP:0011443 abnormal renal water transport IAGP N RGD:5509061 20141003 MGI PMID:10737773 68639 Aqp3 aquaporin 3 gene MP:0031154 intestinal hemorrhage IEA N RGD:5509061 20201015 MGI 68641 Igfals insulin-like growth factor binding protein, acid labile subunit gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:12235108 68641 Igfals insulin-like growth factor binding protein, acid labile subunit gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12235108 68641 Igfals insulin-like growth factor binding protein, acid labile subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10823924 68641 Igfals insulin-like growth factor binding protein, acid labile subunit gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10823924 68641 Igfals insulin-like growth factor binding protein, acid labile subunit gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12235108 68641 Igfals insulin-like growth factor binding protein, acid labile subunit gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:12235108 68641 Igfals insulin-like growth factor binding protein, acid labile subunit gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12235108 68641 Igfals insulin-like growth factor binding protein, acid labile subunit gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:12235108 68641 Igfals insulin-like growth factor binding protein, acid labile subunit gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 68641 Igfals insulin-like growth factor binding protein, acid labile subunit gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20221215 MGI 68641 Igfals insulin-like growth factor binding protein, acid labile subunit gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:12235108 68641 Igfals insulin-like growth factor binding protein, acid labile subunit gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:12235108 68645 Cldn5 claudin 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12743111 68645 Cldn5 claudin 5 gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:12743111 68647 Cldn7 claudin 7 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:19759267 68647 Cldn7 claudin 7 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19759267 68647 Cldn7 claudin 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19759267 68647 Cldn7 claudin 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19759267 68647 Cldn7 claudin 7 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:19759267 68647 Cldn7 claudin 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19759267 68647 Cldn7 claudin 7 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19759267 68647 Cldn7 claudin 7 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19759267 68647 Cldn7 claudin 7 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:19759267 68647 Cldn7 claudin 7 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:19759267 68647 Cldn7 claudin 7 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:19759267 68647 Cldn7 claudin 7 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:19759267 68647 Cldn7 claudin 7 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19759267 68647 Cldn7 claudin 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19759267 68647 Cldn7 claudin 7 gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:19759267 68648 Aqp9 aquaporin 9 gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20190808 MGI 68648 Aqp9 aquaporin 9 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20190808 MGI 68648 Aqp9 aquaporin 9 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17360690 68648 Aqp9 aquaporin 9 gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 68648 Aqp9 aquaporin 9 gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:17360690 68648 Aqp9 aquaporin 9 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17636116 68648 Aqp9 aquaporin 9 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 68648 Aqp9 aquaporin 9 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17636116 68648 Aqp9 aquaporin 9 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17360690 68648 Aqp9 aquaporin 9 gene MP:0031084 decreased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:17636116 68650 Pde10a phosphodiesterase 10A gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:24101672 68650 Pde10a phosphodiesterase 10A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16769090 68650 Pde10a phosphodiesterase 10A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24101672 68650 Pde10a phosphodiesterase 10A gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:18088367 68650 Pde10a phosphodiesterase 10A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16769090 68650 Pde10a phosphodiesterase 10A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170216 MGI PMID:27058446 68650 Pde10a phosphodiesterase 10A gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:16769090 68650 Pde10a phosphodiesterase 10A gene MP:0001462 abnormal avoidance learning behavior IAGP N RGD:5509061 20141003 MGI PMID:16769090 68650 Pde10a phosphodiesterase 10A gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20170216 MGI PMID:27058446 68650 Pde10a phosphodiesterase 10A gene MP:0001525 impaired balance IAGP N RGD:5509061 20170216 MGI PMID:27058446 68650 Pde10a phosphodiesterase 10A gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:24101672 68650 Pde10a phosphodiesterase 10A gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 68650 Pde10a phosphodiesterase 10A gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 68650 Pde10a phosphodiesterase 10A gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:24101672 68650 Pde10a phosphodiesterase 10A gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20170216 MGI PMID:27058446 68650 Pde10a phosphodiesterase 10A gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:24101672 68650 Pde10a phosphodiesterase 10A gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:24101672 68650 Pde10a phosphodiesterase 10A gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:24101672 68650 Pde10a phosphodiesterase 10A gene MP:0005156 bradykinesia IAGP N RGD:5509061 20170216 MGI PMID:27058446 68650 Pde10a phosphodiesterase 10A gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:24101672 68650 Pde10a phosphodiesterase 10A gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20150129 MGI PMID:24698799 68650 Pde10a phosphodiesterase 10A gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16769090 68650 Pde10a phosphodiesterase 10A gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:24101672 68650 Pde10a phosphodiesterase 10A gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:24101672 68650 Pde10a phosphodiesterase 10A gene MP:0006299 abnormal latent inhibition of conditioning behavior IAGP N RGD:5509061 20150129 MGI PMID:24698799 68650 Pde10a phosphodiesterase 10A gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20230119 MGI 68650 Pde10a phosphodiesterase 10A gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:24101672 68650 Pde10a phosphodiesterase 10A gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:24101672 68650 Pde10a phosphodiesterase 10A gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:24101672 68650 Pde10a phosphodiesterase 10A gene MP:0012317 impaired conditioning behavior IAGP N RGD:5509061 20150129 MGI PMID:24698799 68652 Clcnka chloride channel, voltage-sensitive Ka gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:9916798 68652 Clcnka chloride channel, voltage-sensitive Ka gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 68652 Clcnka chloride channel, voltage-sensitive Ka gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:9916798 68652 Clcnka chloride channel, voltage-sensitive Ka gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20240523 MGI 68652 Clcnka chloride channel, voltage-sensitive Ka gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20190404 MGI 68652 Clcnka chloride channel, voltage-sensitive Ka gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20240523 MGI 68654 Gucy1a1 guanylate cyclase 1, soluble, alpha 1 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17679618 68654 Gucy1a1 guanylate cyclase 1, soluble, alpha 1 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:23527308 68654 Gucy1a1 guanylate cyclase 1, soluble, alpha 1 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:16614755 68654 Gucy1a1 guanylate cyclase 1, soluble, alpha 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17679618 68654 Gucy1a1 guanylate cyclase 1, soluble, alpha 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17679618 68654 Gucy1a1 guanylate cyclase 1, soluble, alpha 1 gene MP:0005206 abnormal aqueous humor IAGP N RGD:5509061 20141003 MGI PMID:23527308 68654 Gucy1a1 guanylate cyclase 1, soluble, alpha 1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:23527308 68654 Gucy1a1 guanylate cyclase 1, soluble, alpha 1 gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20141003 MGI PMID:23527308 68654 Gucy1a1 guanylate cyclase 1, soluble, alpha 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16614755 68654 Gucy1a1 guanylate cyclase 1, soluble, alpha 1 gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23527308 68654 Gucy1a1 guanylate cyclase 1, soluble, alpha 1 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:23527308 68654 Gucy1a1 guanylate cyclase 1, soluble, alpha 1 gene MP:0009548 abnormal platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:16614755 68654 Gucy1a1 guanylate cyclase 1, soluble, alpha 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16886062 68654 Gucy1a1 guanylate cyclase 1, soluble, alpha 1 gene MP:0010755 abnormal heart right ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:17679618 68656 Dclk1 doublecortin-like kinase 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:16387639 68656 Dclk1 doublecortin-like kinase 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16387639 68656 Dclk1 doublecortin-like kinase 1 gene MP:0000801 abnormal temporal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 68656 Dclk1 doublecortin-like kinase 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:16387639 68656 Dclk1 doublecortin-like kinase 1 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16387639 68656 Dclk1 doublecortin-like kinase 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16387639 68656 Dclk1 doublecortin-like kinase 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:16387639 68656 Dclk1 doublecortin-like kinase 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:23202126 68656 Dclk1 doublecortin-like kinase 1 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0004794 increased anti-nuclear antigen antibody level IEA N RGD:5509061 20201022 MGI 68656 Dclk1 doublecortin-like kinase 1 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 68656 Dclk1 doublecortin-like kinase 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0006300 abnormal entorhinal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:23202126 68656 Dclk1 doublecortin-like kinase 1 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0008129 absent brain internal capsule IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0008221 abnormal hippocampal commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:16387639 68656 Dclk1 doublecortin-like kinase 1 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16387639 68656 Dclk1 doublecortin-like kinase 1 gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:16387639 68656 Dclk1 doublecortin-like kinase 1 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:16387639 68656 Dclk1 doublecortin-like kinase 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:16387638 68656 Dclk1 doublecortin-like kinase 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 68656 Dclk1 doublecortin-like kinase 1 gene MP:0010093 decreased circulating magnesium level IEA N RGD:5509061 20210128 MGI 68656 Dclk1 doublecortin-like kinase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16387639 68656 Dclk1 doublecortin-like kinase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16387638 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20200402 MGI 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20200402 MGI 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0002425 abnormal susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220811 MGI 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:18234890 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20181227 MGI 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200402 MGI 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:11668339 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20211021 MGI 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20170105 MGI 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:18648504 68660 Bhlhe40 basic helix-loop-helix family, member e40 gene MP:0020475 delayed circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:18648504 68662 Rps19 ribosomal protein S19 gene MP:0000373 belly spot IAGP N RGD:5509061 20181227 MGI PMID:18641651 68662 Rps19 ribosomal protein S19 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 68662 Rps19 ribosomal protein S19 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20181227 MGI PMID:18641651 68662 Rps19 ribosomal protein S19 gene MP:0002095 abnormal skin pigmentation IEA N RGD:5509061 20111116 MGI 68662 Rps19 ribosomal protein S19 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20181227 MGI PMID:18641651 68662 Rps19 ribosomal protein S19 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20181227 MGI PMID:18641651 68662 Rps19 ribosomal protein S19 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20181227 MGI PMID:18641651 68662 Rps19 ribosomal protein S19 gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20181227 MGI PMID:18641651 68662 Rps19 ribosomal protein S19 gene MP:0009387 abnormal epidermal pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 68662 Rps19 ribosomal protein S19 gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20181227 MGI PMID:18641651 68662 Rps19 ribosomal protein S19 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20181227 MGI PMID:18641651 68662 Rps19 ribosomal protein S19 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20181227 MGI PMID:18641651 68662 Rps19 ribosomal protein S19 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12533510 68662 Rps19 ribosomal protein S19 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20181227 MGI PMID:18641651 68662 Rps19 ribosomal protein S19 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15082795 68662 Rps19 ribosomal protein S19 gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12533510 68662 Rps19 ribosomal protein S19 gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 68662 Rps19 ribosomal protein S19 gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 68662 Rps19 ribosomal protein S19 gene MP:0012022 increased melanocyte number IAGP N RGD:5509061 20181227 MGI PMID:18641651 6893651 Fob3b1_m F-line obesity QTL 3b1 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20120914 MGI Created by mouse qtl pipeline PMID:15181539 6893651 Fob3b1_m F-line obesity QTL 3b1 (mouse) qtl MP:0005378 growth/size/body region phenotype IEA N RGD:704405 20120914 MGI Created by mouse qtl pipeline PMID:15181539 68963 Snx1 sorting nexin 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16214895 68963 Snx1 sorting nexin 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:12388759 68963 Snx1 sorting nexin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12388759 68963 Snx1 sorting nexin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12388759 68963 Snx1 sorting nexin 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12388759 68963 Snx1 sorting nexin 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:12388759 68963 Snx1 sorting nexin 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12388759 68963 Snx1 sorting nexin 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12388759 68963 Snx1 sorting nexin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12388759 68963 Snx1 sorting nexin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16214895 68963 Snx1 sorting nexin 1 gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12388759 68963 Snx1 sorting nexin 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12388759 68963 Snx1 sorting nexin 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16214895 68963 Snx1 sorting nexin 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:12388759 68963 Snx1 sorting nexin 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16214895 68963 Snx1 sorting nexin 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12388759 68963 Snx1 sorting nexin 1 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16214895 68963 Snx1 sorting nexin 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12388759 68963 Snx1 sorting nexin 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16214895 68963 Snx1 sorting nexin 1 gene MP:0020515 abnormal visceral yolk sac endoderm morphology IAGP N RGD:5509061 20180125 MGI PMID:12388759 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20190718 MGI PMID:25809849 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20210429 MGI PMID:33029009 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19174523 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19536265 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20190718 MGI PMID:25809849 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20190718 MGI PMID:25809849 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:19174523 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23359070 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20210429 MGI PMID:33029009 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19174523 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:23791182 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:19536265 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20190718 MGI PMID:25809849 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20190718 MGI PMID:25809849 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20190718 MGI PMID:25809849 68967 Eef1a1 eukaryotic translation elongation factor 1 alpha 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:19174523 68975 Wfdc1 WAP four-disulfide core domain 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 68975 Wfdc1 WAP four-disulfide core domain 1 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20150129 MGI PMID:25219356 68975 Wfdc1 WAP four-disulfide core domain 1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20150129 MGI PMID:25219356 68975 Wfdc1 WAP four-disulfide core domain 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20150129 MGI PMID:25219356 68975 Wfdc1 WAP four-disulfide core domain 1 gene MP:0020947 decreased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:25219356 68979 Clu clusterin gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11067863 68979 Clu clusterin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11067863 68979 Clu clusterin gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:11865066 68979 Clu clusterin gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:12145324 68979 Clu clusterin gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:14741101 68979 Clu clusterin gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:11067863 68979 Clu clusterin gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:11067863 68979 Clu clusterin gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:12145324 68979 Clu clusterin gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:14741101 68979 Clu clusterin gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:11067863 68979 Clu clusterin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11067863 68979 Clu clusterin gene MP:0005161 hematuria IAGP N RGD:5509061 20141003 MGI PMID:11865066 68979 Clu clusterin gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11067863 68979 Clu clusterin gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11067863 68979 Clu clusterin gene MP:0005655 increased aggression IEA N RGD:5509061 20160421 MGI 68979 Clu clusterin gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:12145324 68979 Clu clusterin gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:11865066 68979 Clu clusterin gene MP:0011338 abnormal mesangial matrix morphology IAGP N RGD:5509061 20141003 MGI PMID:11865066 68979 Clu clusterin gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:11865066 68979 Clu clusterin gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:11865066 68979 Clu clusterin gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11865066 68979 Clu clusterin gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:11865066 68979 Clu clusterin gene MP:0012270 cardiac edema IAGP N RGD:5509061 20141003 MGI PMID:11067863 68979 Clu clusterin gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 68979 Clu clusterin gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:11865066 68979 Clu clusterin gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:11865066 68979 Clu clusterin gene MP:0021025 increased cerebrospinal fluid amyloid beta 40 isoform level IAGP N RGD:5509061 20220310 MGI PMID:14741101 68979 Clu clusterin gene MP:0021083 increased cerebrospinal fluid amyloid beta 42 isoform level IAGP N RGD:5509061 20220310 MGI PMID:14741101 68981 Tbp TATA box binding protein gene MP:0000160 kyphosis IAGP N RGD:5509061 20151112 MGI PMID:24462098 68981 Tbp TATA box binding protein gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20151112 MGI PMID:21705419 68981 Tbp TATA box binding protein gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20151112 MGI PMID:24462098 68981 Tbp TATA box binding protein gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20151112 MGI PMID:24462098 68981 Tbp TATA box binding protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151112 MGI PMID:24462098 68981 Tbp TATA box binding protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20151112 MGI PMID:21705419 68981 Tbp TATA box binding protein gene MP:0001393 ataxia IAGP N RGD:5509061 20151112 MGI PMID:24462098 68981 Tbp TATA box binding protein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20151112 MGI PMID:21705419 68981 Tbp TATA box binding protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20151112 MGI PMID:21705419 68981 Tbp TATA box binding protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20151112 MGI PMID:24462098 68981 Tbp TATA box binding protein gene MP:0001406 abnormal gait IAGP N RGD:5509061 20151112 MGI PMID:24462098 68981 Tbp TATA box binding protein gene MP:0001407 short stride length IAGP N RGD:5509061 20151112 MGI PMID:24462098 68981 Tbp TATA box binding protein gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20151112 MGI PMID:21705419 68981 Tbp TATA box binding protein gene MP:0001505 hunched posture IAGP N RGD:5509061 20151112 MGI PMID:21705419 68981 Tbp TATA box binding protein gene MP:0001513 limb grasping IAGP N RGD:5509061 20151112 MGI PMID:24462098 68981 Tbp TATA box binding protein gene MP:0001525 impaired balance IAGP N RGD:5509061 20151112 MGI PMID:24462098 68981 Tbp TATA box binding protein gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12411709 68981 Tbp TATA box binding protein gene MP:0002083 premature death IAGP N RGD:5509061 20151112 MGI PMID:24462098 68981 Tbp TATA box binding protein gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:12150996 68981 Tbp TATA box binding protein gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12150996 68981 Tbp TATA box binding protein gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20151112 MGI PMID:21705419 68981 Tbp TATA box binding protein gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20151112 MGI PMID:24462098 68981 Tbp TATA box binding protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12150996 68981 Tbp TATA box binding protein gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12411709 68981 Tbp TATA box binding protein gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12150996 68981 Tbp TATA box binding protein gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:12150996 68981 Tbp TATA box binding protein gene MP:0031070 hemophagocytosis IAGP N RGD:5509061 20200618 MGI PMID:12150996 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:16682631 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:16682631 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:14647484 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:14647484 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16046007 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:16682631 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:16682631 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:16682631 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12576226 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12576226 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0004184 abnormal baroreceptor physiology IAGP N RGD:5509061 20141003 MGI PMID:16682631 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:16682631 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0005523 decreased circulating atrial natriuretic factor IAGP N RGD:5509061 20141003 MGI PMID:16682631 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:12576226 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:15036628 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:12576226 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12576226 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20111116 MGI 68987 Avpr1a arginine vasopressin receptor 1A gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:21621520 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20200402 MGI PMID:31229688 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:21621520 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20200402 MGI PMID:31229688 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20200402 MGI PMID:31229688 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19451696 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15677322 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21621520 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200402 MGI PMID:31229688 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200402 MGI PMID:31229688 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:15677322 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16690884 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20200402 MGI PMID:31229688 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:15677322 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:21621520 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:11498049 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200402 MGI PMID:31229688 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20200402 MGI PMID:31229688 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:19657020 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20200402 MGI PMID:31229688 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:11498049 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20200402 MGI PMID:31229688 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20200402 MGI PMID:31229688 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16690884 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:11498049 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:15677322 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19451696 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0006141 abnormal atrioventricular node conduction IAGP N RGD:5509061 20141003 MGI PMID:16690884 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:16690884 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:11498049 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21621520 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0009436 fragmentation of sleep/wake states IAGP N RGD:5509061 20220922 MGI PMID:15677322 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17525593 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0011953 prolonged PQ interval IAGP N RGD:5509061 20141003 MGI PMID:16690884 68990 Cacna1g calcium channel, voltage-dependent, T type, alpha 1G subunit gene MP:0021198 abnormal sleep duration IAGP N RGD:5509061 20220922 MGI PMID:15677322 68992 Hmox2 heme oxygenase 2 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20210128 MGI 68992 Hmox2 heme oxygenase 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 68992 Hmox2 heme oxygenase 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20170105 MGI 68992 Hmox2 heme oxygenase 2 gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:9486970 68992 Hmox2 heme oxygenase 2 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:15219859 68992 Hmox2 heme oxygenase 2 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:10677545 68992 Hmox2 heme oxygenase 2 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:9486970 68992 Hmox2 heme oxygenase 2 gene MP:0002309 abnormal vital capacity IAGP N RGD:5509061 20141003 MGI PMID:15219859 68992 Hmox2 heme oxygenase 2 gene MP:0002726 abnormal pulmonary vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15219859 68992 Hmox2 heme oxygenase 2 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:10779663 68992 Hmox2 heme oxygenase 2 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:9405702 68992 Hmox2 heme oxygenase 2 gene MP:0004036 abnormal muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:10677545 68992 Hmox2 heme oxygenase 2 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 68992 Hmox2 heme oxygenase 2 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:15219859 68992 Hmox2 heme oxygenase 2 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:15219859 68992 Hmox2 heme oxygenase 2 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:15219859 68992 Hmox2 heme oxygenase 2 gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:9405702 68992 Hmox2 heme oxygenase 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9486970 68992 Hmox2 heme oxygenase 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 68992 Hmox2 heme oxygenase 2 gene MP:0031252 abnormal physiological response to hypoxia IAGP N RGD:5509061 20210805 MGI PMID:34186026 68994 Cacna1h calcium channel, voltage-dependent, T type, alpha 1H subunit gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:24778262 68994 Cacna1h calcium channel, voltage-dependent, T type, alpha 1H subunit gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:14631046 68994 Cacna1h calcium channel, voltage-dependent, T type, alpha 1H subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14631046 68994 Cacna1h calcium channel, voltage-dependent, T type, alpha 1H subunit gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:24778262 68994 Cacna1h calcium channel, voltage-dependent, T type, alpha 1H subunit gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:14631046 68994 Cacna1h calcium channel, voltage-dependent, T type, alpha 1H subunit gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:14631046 68994 Cacna1h calcium channel, voltage-dependent, T type, alpha 1H subunit gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:14631046 68994 Cacna1h calcium channel, voltage-dependent, T type, alpha 1H subunit gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:24778262 68994 Cacna1h calcium channel, voltage-dependent, T type, alpha 1H subunit gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:14631046 68994 Cacna1h calcium channel, voltage-dependent, T type, alpha 1H subunit gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:14631046 68994 Cacna1h calcium channel, voltage-dependent, T type, alpha 1H subunit gene MP:0004112 abnormal arteriole morphology IAGP N RGD:5509061 20141003 MGI PMID:14631046 68994 Cacna1h calcium channel, voltage-dependent, T type, alpha 1H subunit gene MP:0010883 trachea stenosis IAGP N RGD:5509061 20141003 MGI PMID:24778262 68999 Penk preproenkephalin gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 68999 Penk preproenkephalin gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 68999 Penk preproenkephalin gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20170209 MGI PMID:11172058 68999 Penk preproenkephalin gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 68999 Penk preproenkephalin gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20170209 MGI PMID:11172058 68999 Penk preproenkephalin gene MP:0001980 abnormal chemically-elicited antinociception IAGP N RGD:5509061 20170209 MGI PMID:12486185 68999 Penk preproenkephalin gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170209 MGI 68999 Penk preproenkephalin gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20170209 MGI PMID:11172058 68999 Penk preproenkephalin gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201022 MGI 68999 Penk preproenkephalin gene MP:0006415 absent testes IEA N RGD:5509061 20170209 MGI 68999 Penk preproenkephalin gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20170209 MGI PMID:12486185 68999 Penk preproenkephalin gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20170209 MGI PMID:11172058 68999 Penk preproenkephalin gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 68999 Penk preproenkephalin gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:14755340 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:14755340 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14755340 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0001432 abnormal food preference IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14755340 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20160929 MGI PMID:27534441 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0002893 ketoaciduria IAGP N RGD:5509061 20141003 MGI PMID:14755340 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:14755340 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:14755340 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0009351 thin hair shaft IAGP N RGD:5509061 20141003 MGI PMID:14755340 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0011016 increased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14755340 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0011468 abnormal urine amino acid level IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:17767905 69003 Bcat2 branched chain aminotransferase 2, mitochondrial gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:17767905 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18096662 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17660847 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17660847 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20170824 MGI PMID:17289576 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:14566054 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170824 MGI PMID:17289576 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10469645 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:10469645 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:12727921 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:14673173 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11807093 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:23453632 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:10469645 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18453544 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:10469645 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:18096691 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18096662 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:18096691 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14673173 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14673173 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:20215508 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200123 MGI PMID:21576358 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:18096691 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:14566054 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9108058 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:9108058 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9108058 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14673173 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:10469645 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:23453632 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20170824 MGI PMID:17289576 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:21575863 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:10469645 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20215508 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:14566054 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16581004 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18096691 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:23453632 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14673173 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26341559 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17581537 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15021879 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20170824 MGI PMID:17289576 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:12727921 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21575863 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002963 decreased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:14673173 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:18096662 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:14623907 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:20215508 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:14566054 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20170824 MGI PMID:17289576 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14566054 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20170824 MGI PMID:17289576 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:20215508 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20170824 MGI PMID:17289576 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20215508 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16679075 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17660847 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14673173 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:21575863 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:18453544 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0004700 abnormal circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:14673173 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:11807093 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:14566054 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0004937 dilated heart IAGP N RGD:5509061 20170824 MGI PMID:17289576 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17353274 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9794394 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:14673173 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14566054 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170824 MGI PMID:17289576 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:14566054 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:11807093 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16581004 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:14566054 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20170824 MGI PMID:17289576 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:12727921 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18096662 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18096691 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18453544 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20215508 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:18096662 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:14566054 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20170824 MGI PMID:17289576 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9794394 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20170824 MGI PMID:17289576 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20200123 MGI PMID:21576358 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12727921 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17581537 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:12727921 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16679075 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20200123 MGI PMID:21576358 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:21576358 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:21576358 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200123 MGI PMID:21576358 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20200123 MGI PMID:21576358 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:14566054 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15021879 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17581537 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21148800 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:17581537 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:15021879 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12727921 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:21148800 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:11853668 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:14566054 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:14623907 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:17581589 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20141204 MGI PMID:10469645 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:14566054 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141211 MGI PMID:23453632 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0009089 short uterine horn IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18096662 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18096662 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18096662 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:16679075 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20141003 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14673173 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17660847 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10469645 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18096662 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:17363300 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20042677 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20215508 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:14566054 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0010811 decreased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0010858 pulmonary epithelial necrosis IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0010896 decreased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0010935 increased airway resistance IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0011018 pulmonary hyaline membrane formation IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0011044 increased lung elastance IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0011047 increased lung tissue damping IAGP N RGD:5509061 20141003 MGI PMID:14702106 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14673173 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15021879 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9108058 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20215508 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20170824 MGI PMID:17289576 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:15070774 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:9108058 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0012194 decreased keratinocyte migration IAGP N RGD:5509061 20141204 MGI PMID:10469645 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0013807 generalized edema IAGP N RGD:5509061 20170824 MGI PMID:17289576 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0020447 decreased NAD(P)H oxidase activity IAGP N RGD:5509061 20170914 MGI PMID:12571365 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20230615 MGI PMID:20215508 69005 Stat3 signal transducer and activator of transcription 3 gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:18096662 69007 Itga1 integrin alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22297672 69007 Itga1 integrin alpha 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:22297672 69007 Itga1 integrin alpha 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22297672 69007 Itga1 integrin alpha 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11447218 69007 Itga1 integrin alpha 1 gene MP:0002704 tubular nephritis IAGP N RGD:5509061 20141003 MGI PMID:11447218 69007 Itga1 integrin alpha 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:22297672 69007 Itga1 integrin alpha 1 gene MP:0002965 increased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:15277235 69007 Itga1 integrin alpha 1 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:11073824 69007 Itga1 integrin alpha 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:15277235 69007 Itga1 integrin alpha 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15277235 69007 Itga1 integrin alpha 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:22297672 69007 Itga1 integrin alpha 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:15277235 69007 Itga1 integrin alpha 1 gene MP:0005527 increased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:22297672 69007 Itga1 integrin alpha 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:15277235 69007 Itga1 integrin alpha 1 gene MP:0005568 increased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:11073824 69007 Itga1 integrin alpha 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:15277235 69007 Itga1 integrin alpha 1 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:22297672 69007 Itga1 integrin alpha 1 gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:22297672 69007 Itga1 integrin alpha 1 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11073824 69007 Itga1 integrin alpha 1 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:15277235 69007 Itga1 integrin alpha 1 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:22297672 69007 Itga1 integrin alpha 1 gene MP:0011369 increased renal glomerulus apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15277235 69007 Itga1 integrin alpha 1 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:22297672 69007 Itga1 integrin alpha 1 gene MP:0011425 abnormal kidney interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:22297672 69007 Itga1 integrin alpha 1 gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:15277235 69007 Itga1 integrin alpha 1 gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:22297672 69007 Itga1 integrin alpha 1 gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:22297672 69009 Il13 interleukin 13 gene MP:0001263 weight loss IAGP N RGD:5509061 20151015 MGI PMID:24565845 69009 Il13 interleukin 13 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 69009 Il13 interleukin 13 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:10330435 69009 Il13 interleukin 13 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:10679097 69009 Il13 interleukin 13 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:12150887 69009 Il13 interleukin 13 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:18250447 69009 Il13 interleukin 13 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:10330435 69009 Il13 interleukin 13 gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:18250480 69009 Il13 interleukin 13 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:10679097 69009 Il13 interleukin 13 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:20937871 69009 Il13 interleukin 13 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20151015 MGI PMID:17400729 69009 Il13 interleukin 13 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21573182 69009 Il13 interleukin 13 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18250480 69009 Il13 interleukin 13 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:21573182 69009 Il13 interleukin 13 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:17182558 69009 Il13 interleukin 13 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11591797 69009 Il13 interleukin 13 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11745342 69009 Il13 interleukin 13 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12150887 69009 Il13 interleukin 13 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:9768762 69009 Il13 interleukin 13 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9768762 69009 Il13 interleukin 13 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:11070175 69009 Il13 interleukin 13 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:12150887 69009 Il13 interleukin 13 gene MP:0002531 abnormal type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10861042 69009 Il13 interleukin 13 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11070175 69009 Il13 interleukin 13 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12150887 69009 Il13 interleukin 13 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18250480 69009 Il13 interleukin 13 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:16816360 69009 Il13 interleukin 13 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:18250480 69009 Il13 interleukin 13 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12150887 69009 Il13 interleukin 13 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11070175 69009 Il13 interleukin 13 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20200518 69009 Il13 interleukin 13 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22138715 69009 Il13 interleukin 13 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:10679097 69009 Il13 interleukin 13 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:11745342 69009 Il13 interleukin 13 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:10330435 69009 Il13 interleukin 13 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:10679097 69009 Il13 interleukin 13 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:12150887 69009 Il13 interleukin 13 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:22138715 69009 Il13 interleukin 13 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:12540780 69009 Il13 interleukin 13 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:15034018 69009 Il13 interleukin 13 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22101429 69009 Il13 interleukin 13 gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:11591797 69009 Il13 interleukin 13 gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:17182558 69009 Il13 interleukin 13 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11591797 69009 Il13 interleukin 13 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:10330435 69009 Il13 interleukin 13 gene MP:0005575 increased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 69009 Il13 interleukin 13 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10861042 69009 Il13 interleukin 13 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:16816360 69009 Il13 interleukin 13 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11070175 69009 Il13 interleukin 13 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:17611223 69009 Il13 interleukin 13 gene MP:0008091 decreased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:9768762 69009 Il13 interleukin 13 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9768762 69009 Il13 interleukin 13 gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17182558 69009 Il13 interleukin 13 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11745342 69009 Il13 interleukin 13 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22138715 69009 Il13 interleukin 13 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:11591797 69009 Il13 interleukin 13 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:9768762 69009 Il13 interleukin 13 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17182558 69009 Il13 interleukin 13 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9768762 69009 Il13 interleukin 13 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11591797 69009 Il13 interleukin 13 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:11070175 69009 Il13 interleukin 13 gene MP:0008609 decreased circulating interleukin-13 level IAGP N RGD:5509061 20141003 MGI PMID:9768762 69009 Il13 interleukin 13 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:9768762 69009 Il13 interleukin 13 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:11323701 69009 Il13 interleukin 13 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:11591797 69009 Il13 interleukin 13 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:17182558 69009 Il13 interleukin 13 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:22138715 69009 Il13 interleukin 13 gene MP:0008698 abnormal interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:11591797 69009 Il13 interleukin 13 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:11070175 69009 Il13 interleukin 13 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:11323701 69009 Il13 interleukin 13 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:9768762 69009 Il13 interleukin 13 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:11070175 69009 Il13 interleukin 13 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:11591797 69009 Il13 interleukin 13 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:17182558 69009 Il13 interleukin 13 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:22138715 69009 Il13 interleukin 13 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:9768762 69009 Il13 interleukin 13 gene MP:0008712 decreased interleukin-9 secretion IAGP N RGD:5509061 20141003 MGI PMID:11070175 69009 Il13 interleukin 13 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:12540780 69009 Il13 interleukin 13 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:18250447 69009 Il13 interleukin 13 gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:11950906 69009 Il13 interleukin 13 gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10679097 69009 Il13 interleukin 13 gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11745342 69009 Il13 interleukin 13 gene MP:0009482 ileum inflammation IAGP N RGD:5509061 20141003 MGI PMID:10679097 69009 Il13 interleukin 13 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:22101429 69009 Il13 interleukin 13 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20151015 MGI PMID:24565845 69009 Il13 interleukin 13 gene MP:0010750 increased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10679097 69009 Il13 interleukin 13 gene MP:0010751 decreased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10679097 69009 Il13 interleukin 13 gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:22101429 69009 Il13 interleukin 13 gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:22101429 69016 Ryr3 ryanodine receptor 3 gene MP:0000738 impaired muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9384575 69016 Ryr3 ryanodine receptor 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:8702664 69016 Ryr3 ryanodine receptor 3 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10595520 69016 Ryr3 ryanodine receptor 3 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10719224 69016 Ryr3 ryanodine receptor 3 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:10719224 69016 Ryr3 ryanodine receptor 3 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:10595520 69016 Ryr3 ryanodine receptor 3 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10595520 69016 Ryr3 ryanodine receptor 3 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:10719224 69016 Ryr3 ryanodine receptor 3 gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10581317 69016 Ryr3 ryanodine receptor 3 gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9384575 69016 Ryr3 ryanodine receptor 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:8702664 69019 Stmn3 stathmin-like 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 69019 Stmn3 stathmin-like 3 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 69021 Gnal guanine nucleotide binding protein, alpha stimulating, olfactory type gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9459443 69021 Gnal guanine nucleotide binding protein, alpha stimulating, olfactory type gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:9459443 69021 Gnal guanine nucleotide binding protein, alpha stimulating, olfactory type gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:9459443 69021 Gnal guanine nucleotide binding protein, alpha stimulating, olfactory type gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9459443 69021 Gnal guanine nucleotide binding protein, alpha stimulating, olfactory type gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:9459443 69021 Gnal guanine nucleotide binding protein, alpha stimulating, olfactory type gene MP:0003462 abnormal response to novel odor IAGP N RGD:5509061 20141003 MGI PMID:9459443 69021 Gnal guanine nucleotide binding protein, alpha stimulating, olfactory type gene MP:0009326 absent maternal crouching IAGP N RGD:5509061 20141003 MGI PMID:9459443 69021 Gnal guanine nucleotide binding protein, alpha stimulating, olfactory type gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9459443 69021 Gnal guanine nucleotide binding protein, alpha stimulating, olfactory type gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:9459443 69023 Fdps farnesyl diphosphate synthetase gene MP:0000274 enlarged heart IAGP N RGD:5509061 20220203 MGI PMID:34467534 69023 Fdps farnesyl diphosphate synthetase gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20220203 MGI PMID:34467534 69023 Fdps farnesyl diphosphate synthetase gene MP:0002083 premature death IAGP N RGD:5509061 20220203 MGI PMID:34467534 69023 Fdps farnesyl diphosphate synthetase gene MP:0002833 increased heart weight IAGP N RGD:5509061 20220203 MGI PMID:34467534 69023 Fdps farnesyl diphosphate synthetase gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20220203 MGI PMID:34467534 69023 Fdps farnesyl diphosphate synthetase gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20220203 MGI PMID:34467534 69023 Fdps farnesyl diphosphate synthetase gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20220203 MGI PMID:34467534 69023 Fdps farnesyl diphosphate synthetase gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20220203 MGI PMID:34467534 69023 Fdps farnesyl diphosphate synthetase gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20220203 MGI PMID:34467534 69023 Fdps farnesyl diphosphate synthetase gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20220203 MGI PMID:34467534 69025 H19 H19, imprinted maternally expressed transcript gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:11846487 69025 H19 H19, imprinted maternally expressed transcript gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:11846487 69025 H19 H19, imprinted maternally expressed transcript gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11846487 69025 H19 H19, imprinted maternally expressed transcript gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:7536897 69025 H19 H19, imprinted maternally expressed transcript gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:9203585 69025 H19 H19, imprinted maternally expressed transcript gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14681296 69025 H19 H19, imprinted maternally expressed transcript gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16416086 69025 H19 H19, imprinted maternally expressed transcript gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18719115 69025 H19 H19, imprinted maternally expressed transcript gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:11846487 69025 H19 H19, imprinted maternally expressed transcript gene MP:0003121 genetic imprinting IAGP N RGD:5509061 20141003 MGI PMID:10449763 69025 H19 H19, imprinted maternally expressed transcript gene MP:0003121 genetic imprinting IAGP N RGD:5509061 20141003 MGI PMID:9679064 69025 H19 H19, imprinted maternally expressed transcript gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:11846487 69025 H19 H19, imprinted maternally expressed transcript gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:7536897 69025 H19 H19, imprinted maternally expressed transcript gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:18719115 69025 H19 H19, imprinted maternally expressed transcript gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:18719115 69025 H19 H19, imprinted maternally expressed transcript gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:11846487 69025 H19 H19, imprinted maternally expressed transcript gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:11846487 69025 H19 H19, imprinted maternally expressed transcript gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14681296 69025 H19 H19, imprinted maternally expressed transcript gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:11846487 69025 H19 H19, imprinted maternally expressed transcript gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:11846487 69025 H19 H19, imprinted maternally expressed transcript gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:12270940 69025 H19 H19, imprinted maternally expressed transcript gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18719115 69025 H19 H19, imprinted maternally expressed transcript gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11846487 69025 H19 H19, imprinted maternally expressed transcript gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11846487 69027 Prkcd protein kinase C, delta gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15232611 69027 Prkcd protein kinase C, delta gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11976687 69027 Prkcd protein kinase C, delta gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11976687 69027 Prkcd protein kinase C, delta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17135234 69027 Prkcd protein kinase C, delta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21576825 69027 Prkcd protein kinase C, delta gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11714742 69027 Prkcd protein kinase C, delta gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21576825 69027 Prkcd protein kinase C, delta gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:11976687 69027 Prkcd protein kinase C, delta gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:15232611 69027 Prkcd protein kinase C, delta gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20151231 MGI PMID:25505183 69027 Prkcd protein kinase C, delta gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11976687 69027 Prkcd protein kinase C, delta gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:11976687 69027 Prkcd protein kinase C, delta gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21576825 69027 Prkcd protein kinase C, delta gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17135234 69027 Prkcd protein kinase C, delta gene MP:0003075 abnormal response to CNS ischemic injury IAGP N RGD:5509061 20141003 MGI PMID:15232611 69027 Prkcd protein kinase C, delta gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17199045 69027 Prkcd protein kinase C, delta gene MP:0003991 arteriosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11714742 69027 Prkcd protein kinase C, delta gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:11976687 69027 Prkcd protein kinase C, delta gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0005005 abnormal self tolerance IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11976687 69027 Prkcd protein kinase C, delta gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:11976687 69027 Prkcd protein kinase C, delta gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11976687 69027 Prkcd protein kinase C, delta gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17135234 69027 Prkcd protein kinase C, delta gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21576825 69027 Prkcd protein kinase C, delta gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17135234 69027 Prkcd protein kinase C, delta gene MP:0005489 vascular smooth muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11714742 69027 Prkcd protein kinase C, delta gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:11714742 69027 Prkcd protein kinase C, delta gene MP:0008044 increased NK cell number IEA N RGD:5509061 20181011 MGI 69027 Prkcd protein kinase C, delta gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17199045 69027 Prkcd protein kinase C, delta gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:17199045 69027 Prkcd protein kinase C, delta gene MP:0008471 abnormal spleen primary B follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:11976687 69027 Prkcd protein kinase C, delta gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11976687 69027 Prkcd protein kinase C, delta gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:11976687 69027 Prkcd protein kinase C, delta gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20181011 MGI 69027 Prkcd protein kinase C, delta gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:11976687 69027 Prkcd protein kinase C, delta gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11976686 69027 Prkcd protein kinase C, delta gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16481047 69027 Prkcd protein kinase C, delta gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21576825 69027 Prkcd protein kinase C, delta gene MP:0020155 enhanced humoral immune response IEA N RGD:5509061 20181011 MGI 69027 Prkcd protein kinase C, delta gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:11976687 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0000111 cleft palate IEA N RGD:5509061 20170209 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0000445 short snout IEA N RGD:5509061 20170209 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0000562 polydactyly IEA N RGD:5509061 20170209 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20170209 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20170209 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20170209 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20230601 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20170209 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0002639 micrognathia IEA N RGD:5509061 20170209 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20231207 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0003321 tracheoesophageal fistula IEA N RGD:5509061 20170209 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0009743 preaxial polydactyly IEA N RGD:5509061 20170209 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20170209 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0010466 vascular ring IEA N RGD:5509061 20170209 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0010488 abnormal left subclavian artery morphology IEA N RGD:5509061 20170209 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20230601 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0011971 increased circulating lactate dehydrogenase level IEA N RGD:5509061 20230601 MGI 69036 Qsox1 quiescin Q6 sulfhydryl oxidase 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 69039 Igfbp1 insulin-like growth factor binding protein 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:12511596 69039 Igfbp1 insulin-like growth factor binding protein 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:12556485 69039 Igfbp1 insulin-like growth factor binding protein 1 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:12511596 69039 Igfbp1 insulin-like growth factor binding protein 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:12511596 69039 Igfbp1 insulin-like growth factor binding protein 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12511596 69039 Igfbp1 insulin-like growth factor binding protein 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12511596 69039 Igfbp1 insulin-like growth factor binding protein 1 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:12556485 69039 Igfbp1 insulin-like growth factor binding protein 1 gene MP:0031324 delayed liver regeneration IAGP N RGD:5509061 20220106 MGI PMID:12556485 69041 S100a4 S100 calcium binding protein A4 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15116098 69041 S100a4 S100 calcium binding protein A4 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15116098 69041 S100a4 S100 calcium binding protein A4 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15116098 69041 S100a4 S100 calcium binding protein A4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12810675 69041 S100a4 S100 calcium binding protein A4 gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20141003 MGI PMID:20519440 69041 S100a4 S100 calcium binding protein A4 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15116098 69041 S100a4 S100 calcium binding protein A4 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20230119 MGI PMID:35982178 69041 S100a4 S100 calcium binding protein A4 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20230119 MGI PMID:35982178 69041 S100a4 S100 calcium binding protein A4 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20519440 69041 S100a4 S100 calcium binding protein A4 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15116098 69041 S100a4 S100 calcium binding protein A4 gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15116098 69041 S100a4 S100 calcium binding protein A4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15116098 69041 S100a4 S100 calcium binding protein A4 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15116098 69086 Adam2 a disintegrin and metallopeptidase domain 2 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20191226 MGI PMID:11319869 69086 Adam2 a disintegrin and metallopeptidase domain 2 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20191226 MGI PMID:9743500 69086 Adam2 a disintegrin and metallopeptidase domain 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:9743500 69086 Adam2 a disintegrin and metallopeptidase domain 2 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191017 MGI PMID:9743500 69086 Adam2 a disintegrin and metallopeptidase domain 2 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20200227 MGI PMID:9743500 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:10224224 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20141003 MGI 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0001304 cataract IEA N RGD:5509061 20141003 MGI 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:10224224 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10224224 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10224224 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:10224224 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16249436 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0002899 fatigue IAGP N RGD:5509061 20141003 MGI PMID:10224224 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16249436 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10224224 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0010358 abnormal free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:21044951 69088 Fabp3 fatty acid binding protein 3, muscle and heart gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:10224224 69092 Smad4 SMAD family member 4 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:20877696 69092 Smad4 SMAD family member 4 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:16887829 69092 Smad4 SMAD family member 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9420335 69092 Smad4 SMAD family member 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0000381 enlarged hair follicles IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16518688 69092 Smad4 SMAD family member 4 gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:16518688 69092 Smad4 SMAD family member 4 gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:16518688 69092 Smad4 SMAD family member 4 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:16518688 69092 Smad4 SMAD family member 4 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:15342483 69092 Smad4 SMAD family member 4 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:15342483 69092 Smad4 SMAD family member 4 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:16767220 69092 Smad4 SMAD family member 4 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:23999427 69092 Smad4 SMAD family member 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16288217 69092 Smad4 SMAD family member 4 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:17213286 69092 Smad4 SMAD family member 4 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:12896967 69092 Smad4 SMAD family member 4 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:12896967 69092 Smad4 SMAD family member 4 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:15215210 69092 Smad4 SMAD family member 4 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:16513794 69092 Smad4 SMAD family member 4 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16513794 69092 Smad4 SMAD family member 4 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22341455 69092 Smad4 SMAD family member 4 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23999427 69092 Smad4 SMAD family member 4 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20150514 MGI PMID:24784840 69092 Smad4 SMAD family member 4 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16288217 69092 Smad4 SMAD family member 4 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20573697 69092 Smad4 SMAD family member 4 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:9420335 69092 Smad4 SMAD family member 4 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:9420335 69092 Smad4 SMAD family member 4 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:12432092 69092 Smad4 SMAD family member 4 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9420335 69092 Smad4 SMAD family member 4 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:15215210 69092 Smad4 SMAD family member 4 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:9420335 69092 Smad4 SMAD family member 4 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:12432092 69092 Smad4 SMAD family member 4 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:9420335 69092 Smad4 SMAD family member 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9420335 69092 Smad4 SMAD family member 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15215210 69092 Smad4 SMAD family member 4 gene MP:0001705 abnormal proximal-distal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15215210 69092 Smad4 SMAD family member 4 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:15215210 69092 Smad4 SMAD family member 4 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9420335 69092 Smad4 SMAD family member 4 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19578404 69092 Smad4 SMAD family member 4 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20150514 MGI PMID:24784840 69092 Smad4 SMAD family member 4 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:16513794 69092 Smad4 SMAD family member 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:16513794 69092 Smad4 SMAD family member 4 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20160929 MGI PMID:25803032 69092 Smad4 SMAD family member 4 gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:23999427 69092 Smad4 SMAD family member 4 gene MP:0002015 epithelioid cyst IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16518688 69092 Smad4 SMAD family member 4 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17114584 69092 Smad4 SMAD family member 4 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19002110 69092 Smad4 SMAD family member 4 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:23999427 69092 Smad4 SMAD family member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15342483 69092 Smad4 SMAD family member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16288217 69092 Smad4 SMAD family member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16767220 69092 Smad4 SMAD family member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22341455 69092 Smad4 SMAD family member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9506519 69092 Smad4 SMAD family member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20150514 MGI PMID:24784840 69092 Smad4 SMAD family member 4 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9420335 69092 Smad4 SMAD family member 4 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12432092 69092 Smad4 SMAD family member 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17300215 69092 Smad4 SMAD family member 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12557227 69092 Smad4 SMAD family member 4 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16288217 69092 Smad4 SMAD family member 4 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12896967 69092 Smad4 SMAD family member 4 gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:9420335 69092 Smad4 SMAD family member 4 gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16767220 69092 Smad4 SMAD family member 4 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0002732 increased trichoepithelioma incidence IAGP N RGD:5509061 20141003 MGI PMID:23999427 69092 Smad4 SMAD family member 4 gene MP:0002764 short tibia IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16767220 69092 Smad4 SMAD family member 4 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16288217 69092 Smad4 SMAD family member 4 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9506519 69092 Smad4 SMAD family member 4 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20150514 MGI PMID:24784840 69092 Smad4 SMAD family member 4 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16767220 69092 Smad4 SMAD family member 4 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:15342483 69092 Smad4 SMAD family member 4 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16887829 69092 Smad4 SMAD family member 4 gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:16288217 69092 Smad4 SMAD family member 4 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:16518688 69092 Smad4 SMAD family member 4 gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:10626800 69092 Smad4 SMAD family member 4 gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:16288217 69092 Smad4 SMAD family member 4 gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:16518688 69092 Smad4 SMAD family member 4 gene MP:0003334 pancreas fibrosis IAGP N RGD:5509061 20160929 MGI PMID:25803032 69092 Smad4 SMAD family member 4 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:17114584 69092 Smad4 SMAD family member 4 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20160929 MGI PMID:25803032 69092 Smad4 SMAD family member 4 gene MP:0003341 chronic pancreas inflammation IAGP N RGD:5509061 20160929 MGI PMID:25803032 69092 Smad4 SMAD family member 4 gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:16513794 69092 Smad4 SMAD family member 4 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16887829 69092 Smad4 SMAD family member 4 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:23999427 69092 Smad4 SMAD family member 4 gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:9506519 69092 Smad4 SMAD family member 4 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:19002110 69092 Smad4 SMAD family member 4 gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20160929 MGI PMID:25803032 69092 Smad4 SMAD family member 4 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:15342483 69092 Smad4 SMAD family member 4 gene MP:0003705 abnormal hypodermis morphology IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:17213286 69092 Smad4 SMAD family member 4 gene MP:0003875 abnormal hair follicle regression IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:15215210 69092 Smad4 SMAD family member 4 gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:9420335 69092 Smad4 SMAD family member 4 gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20877696 69092 Smad4 SMAD family member 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12432092 69092 Smad4 SMAD family member 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12557227 69092 Smad4 SMAD family member 4 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:16887829 69092 Smad4 SMAD family member 4 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:20877696 69092 Smad4 SMAD family member 4 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20150514 MGI PMID:24784840 69092 Smad4 SMAD family member 4 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0004675 rib fractures IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23221368 69092 Smad4 SMAD family member 4 gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:16513794 69092 Smad4 SMAD family member 4 gene MP:0005210 disorganized stomach mucosa IAGP N RGD:5509061 20141003 MGI PMID:16518688 69092 Smad4 SMAD family member 4 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20160929 MGI PMID:25803032 69092 Smad4 SMAD family member 4 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15215210 69092 Smad4 SMAD family member 4 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:15342483 69092 Smad4 SMAD family member 4 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:16513794 69092 Smad4 SMAD family member 4 gene MP:0005493 stomach epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12557227 69092 Smad4 SMAD family member 4 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:15215210 69092 Smad4 SMAD family member 4 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16518688 69092 Smad4 SMAD family member 4 gene MP:0008010 increased gastric adenocarcinoma incidence IAGP N RGD:5509061 20150514 MGI PMID:24784840 69092 Smad4 SMAD family member 4 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:16288217 69092 Smad4 SMAD family member 4 gene MP:0008012 duodenum polyps IAGP N RGD:5509061 20141003 MGI PMID:10626800 69092 Smad4 SMAD family member 4 gene MP:0008012 duodenum polyps IAGP N RGD:5509061 20141003 MGI PMID:17114584 69092 Smad4 SMAD family member 4 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16518688 69092 Smad4 SMAD family member 4 gene MP:0008156 decreased diameter of tibia IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0008393 absent primordial germ cells IAGP N RGD:5509061 20141003 MGI PMID:15215210 69092 Smad4 SMAD family member 4 gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16513794 69092 Smad4 SMAD family member 4 gene MP:0009143 abnormal pancreatic duct morphology IAGP N RGD:5509061 20160929 MGI PMID:25803032 69092 Smad4 SMAD family member 4 gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20160929 MGI PMID:25803032 69092 Smad4 SMAD family member 4 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20160929 MGI PMID:25803032 69092 Smad4 SMAD family member 4 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17114584 69092 Smad4 SMAD family member 4 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9506519 69092 Smad4 SMAD family member 4 gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20160929 MGI PMID:25803032 69092 Smad4 SMAD family member 4 gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22341455 69092 Smad4 SMAD family member 4 gene MP:0009311 increased duodenum adenocarcinoma incidence IAGP N RGD:5509061 20150514 MGI PMID:24784840 69092 Smad4 SMAD family member 4 gene MP:0009373 abnormal cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:16513794 69092 Smad4 SMAD family member 4 gene MP:0009374 absent cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:16513794 69092 Smad4 SMAD family member 4 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23999427 69092 Smad4 SMAD family member 4 gene MP:0009715 thick epidermis stratum basale IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20170309 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0010224 abnormal heart ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:20877696 69092 Smad4 SMAD family member 4 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19578404 69092 Smad4 SMAD family member 4 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23999427 69092 Smad4 SMAD family member 4 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12557227 69092 Smad4 SMAD family member 4 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15215210 69092 Smad4 SMAD family member 4 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16518688 69092 Smad4 SMAD family member 4 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17114584 69092 Smad4 SMAD family member 4 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16767220 69092 Smad4 SMAD family member 4 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23999427 69092 Smad4 SMAD family member 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20877696 69092 Smad4 SMAD family member 4 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:20877696 69092 Smad4 SMAD family member 4 gene MP:0010690 thick hair follicle outer root sheath IAGP N RGD:5509061 20141003 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0010970 abnormal compact bone lamellar structure IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15342483 69092 Smad4 SMAD family member 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15342483 69092 Smad4 SMAD family member 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12557227 69092 Smad4 SMAD family member 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20877696 69092 Smad4 SMAD family member 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12896967 69092 Smad4 SMAD family member 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11857783 69092 Smad4 SMAD family member 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12432092 69092 Smad4 SMAD family member 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9420335 69092 Smad4 SMAD family member 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9506519 69092 Smad4 SMAD family member 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15215210 69092 Smad4 SMAD family member 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16887829 69092 Smad4 SMAD family member 4 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20877696 69092 Smad4 SMAD family member 4 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:16513794 69092 Smad4 SMAD family member 4 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15215210 69092 Smad4 SMAD family member 4 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9420335 69092 Smad4 SMAD family member 4 gene MP:0011192 decreased embryonic epiblast cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0011642 abnormal bone collagen fibril morphology IAGP N RGD:5509061 20141120 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:15215210 69092 Smad4 SMAD family member 4 gene MP:0011846 decreased kidney collecting duct number IAGP N RGD:5509061 20141003 MGI PMID:15342483 69092 Smad4 SMAD family member 4 gene MP:0012083 absent foregut IAGP N RGD:5509061 20141003 MGI PMID:15215210 69092 Smad4 SMAD family member 4 gene MP:0012086 absent hindgut IAGP N RGD:5509061 20141003 MGI PMID:15215210 69092 Smad4 SMAD family member 4 gene MP:0012095 increased Reichert's membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:9520423 69092 Smad4 SMAD family member 4 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:9420335 69092 Smad4 SMAD family member 4 gene MP:0012159 absent anterior visceral endoderm IAGP N RGD:5509061 20141003 MGI PMID:20573697 69092 Smad4 SMAD family member 4 gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20160929 MGI PMID:25803032 69092 Smad4 SMAD family member 4 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:16288217 69092 Smad4 SMAD family member 4 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:17114584 69092 Smad4 SMAD family member 4 gene MP:0021106 abnormal secondary ovarian follicle morphology IAGP N RGD:5509061 20220407 MGI PMID:16513794 69092 Smad4 SMAD family member 4 gene MP:0030079 small incisors IAGP N RGD:5509061 20170928 MGI PMID:24006258 69092 Smad4 SMAD family member 4 gene MP:0030574 increased hair follicle cell proliferation IAGP N RGD:5509061 20181129 MGI PMID:16204035 69092 Smad4 SMAD family member 4 gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:16513794 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000129 ameloblast degeneration IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15922720 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000597 delayed hepatic development IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19415629 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:11168809 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11342667 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19415629 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001652 colonic necrosis IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001653 gastric necrosis IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001653 gastric necrosis IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:11342667 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001655 multifocal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:18343643 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:18544680 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15922720 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19415629 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:19415629 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15922720 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:19415629 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:11342667 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001854 atrial endocarditis IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001857 pericarditis IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11342667 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:21435587 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:11342667 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:19415629 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:21435587 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:19415629 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15922720 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:18343643 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18343643 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11168809 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11168809 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11342667 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15922720 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21435587 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20150205 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15922720 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:19415629 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:21435587 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002817 abnormal tooth mineralization IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:11342667 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0003282 gastric ulcer IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0003305 proctitis IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0003353 decreased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0003543 abnormal vascular endothelial cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0003865 lymph node inflammation IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:19415629 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004041 increased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:18434384 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:18434384 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21435587 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:23569233 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004820 abnormal urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23645881 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18343643 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19415629 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:19415629 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21435587 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23569233 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:11342667 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:15922720 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:21435587 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:18434384 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005628 decreased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0006375 increased circulating angiotensinogen level IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0006376 decreased circulating angiotensinogen level IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008010 increased gastric adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11342667 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11342667 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:11342667 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:21435587 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:23569233 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008118 absent Langerhans cell IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008118 absent Langerhans cell IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008119 decreased Langerhans cell number IAGP N RGD:5509061 20141003 MGI PMID:17938236 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20150205 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:11168809 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11342667 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19415629 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19415629 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18434384 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141211 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21435587 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0009310 increased large intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0009315 increased rectum adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0009316 increased anal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0009856 failure of ejaculation IAGP N RGD:5509061 20141003 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221201 MGI PMID:18343643 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0010096 abnormal incisor color IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0010127 hypervolemia IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0010128 hypovolemia IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0010140 phlebitis IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:21435587 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21435587 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19022904 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15922720 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11342667 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11342667 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18343643 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18343643 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11342667 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18343643 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8421714 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18343643 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:17353357 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:18343643 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011460 decreased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:23503843 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:7600998 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0013467 diaphragmitis IAGP N RGD:5509061 20150205 MGI PMID:1436033 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0014269 decreased testes secretion IAGP N RGD:5509061 20230810 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:17481928 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0030459 abnormal tooth attrition IAGP N RGD:5509061 20180125 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20180125 MGI PMID:24056369 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0030983 failure of copulatory plug deposition IAGP N RGD:5509061 20191017 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0031628 abnormal intromission IAGP N RGD:5509061 20240718 MGI PMID:17478551 69096 Tgfb1 transforming growth factor, beta 1 gene MP:0031650 decreased mounting behavior IAGP N RGD:5509061 20240905 MGI PMID:17478551 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11319559 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:11375491 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:11375491 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16530794 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16530794 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16530794 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:16530794 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:16530794 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11319559 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15561946 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20201231 MGI 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:16530794 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0002711 decreased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:11319559 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0002711 decreased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:17503968 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9724715 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:16530794 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11029282 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17510189 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:9724715 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15561946 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17503968 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15561946 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20141003 MGI PMID:20074528 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16530794 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:20074528 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:11319559 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:11375491 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0003479 abnormal nerve fiber response intensity IAGP N RGD:5509061 20141003 MGI PMID:11375491 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15561946 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:17510189 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:11375491 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0004036 abnormal muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:11029282 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15949470 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:20074528 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:20074528 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15561946 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15561946 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:9724715 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:15949470 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:11319559 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:20074528 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0005522 increased circulating atrial natriuretic factor IAGP N RGD:5509061 20141003 MGI PMID:15949470 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15561946 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:20074528 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:16530794 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:20074528 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20074528 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0009287 decreased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:20074528 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11375491 69099 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 69103 Jak1 Janus kinase 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141016 MGI PMID:22527485 69103 Jak1 Janus kinase 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141016 MGI PMID:22527485 69103 Jak1 Janus kinase 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:9590172 69103 Jak1 Janus kinase 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:9590172 69103 Jak1 Janus kinase 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9590172 69103 Jak1 Janus kinase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141016 MGI PMID:22527485 69103 Jak1 Janus kinase 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9590172 69103 Jak1 Janus kinase 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9590172 69103 Jak1 Janus kinase 1 gene MP:0001849 ear inflammation IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0001957 apnea IAGP N RGD:5509061 20161013 MGI PMID:27671227 69103 Jak1 Janus kinase 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9590172 69103 Jak1 Janus kinase 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9590172 69103 Jak1 Janus kinase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20161013 MGI PMID:27671227 69103 Jak1 Janus kinase 1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141016 MGI PMID:22527485 69103 Jak1 Janus kinase 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9590172 69103 Jak1 Janus kinase 1 gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141016 MGI PMID:22527485 69103 Jak1 Janus kinase 1 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20161013 MGI PMID:27671227 69103 Jak1 Janus kinase 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0004945 abnormal bone resorption IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9590172 69103 Jak1 Janus kinase 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:9590172 69103 Jak1 Janus kinase 1 gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0005328 abnormal circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0005516 enhanced liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20161013 MGI PMID:27044867 69103 Jak1 Janus kinase 1 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0008935 decreased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0008956 decreased cellular hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0010965 decreased compact bone volume IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9590172 69103 Jak1 Janus kinase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20161013 MGI PMID:27671227 69103 Jak1 Janus kinase 1 gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0011467 decreased urine urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23791841 69103 Jak1 Janus kinase 1 gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20141003 MGI PMID:23791841 69106 Nr1i2 nuclear receptor subfamily 1, group I, member 2 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19815629 69106 Nr1i2 nuclear receptor subfamily 1, group I, member 2 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20151112 MGI PMID:22467028 69106 Nr1i2 nuclear receptor subfamily 1, group I, member 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:11248085 69106 Nr1i2 nuclear receptor subfamily 1, group I, member 2 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11248085 69106 Nr1i2 nuclear receptor subfamily 1, group I, member 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18677425 69106 Nr1i2 nuclear receptor subfamily 1, group I, member 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10935643 69106 Nr1i2 nuclear receptor subfamily 1, group I, member 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11602523 69106 Nr1i2 nuclear receptor subfamily 1, group I, member 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18677425 69106 Nr1i2 nuclear receptor subfamily 1, group I, member 2 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11248085 69109 Matk megakaryocyte-associated tyrosine kinase gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:16574955 69109 Matk megakaryocyte-associated tyrosine kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8694808 69109 Matk megakaryocyte-associated tyrosine kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9315289 69109 Matk megakaryocyte-associated tyrosine kinase gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16574955 69109 Matk megakaryocyte-associated tyrosine kinase gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:16574955 69110 Gata2 GATA binding protein 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12077323 69110 Gata2 GATA binding protein 2 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:8078582 69110 Gata2 GATA binding protein 2 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:18233958 69110 Gata2 GATA binding protein 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:18233958 69110 Gata2 GATA binding protein 2 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:18233958 69110 Gata2 GATA binding protein 2 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 69110 Gata2 GATA binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18233958 69110 Gata2 GATA binding protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18233958 69110 Gata2 GATA binding protein 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16543408 69110 Gata2 GATA binding protein 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20838598 69110 Gata2 GATA binding protein 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8078582 69110 Gata2 GATA binding protein 2 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8078582 69110 Gata2 GATA binding protein 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221103 MGI 69110 Gata2 GATA binding protein 2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:8078582 69110 Gata2 GATA binding protein 2 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:8078582 69110 Gata2 GATA binding protein 2 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20220512 MGI PMID:27783953 69110 Gata2 GATA binding protein 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16543408 69110 Gata2 GATA binding protein 2 gene MP:0001746 abnormal pituitary secretion IAGP N RGD:5509061 20141003 MGI PMID:16543408 69110 Gata2 GATA binding protein 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20220512 MGI PMID:27783953 69110 Gata2 GATA binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18233958 69110 Gata2 GATA binding protein 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12689939 69110 Gata2 GATA binding protein 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16461905 69110 Gata2 GATA binding protein 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:18233958 69110 Gata2 GATA binding protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16461905 69110 Gata2 GATA binding protein 2 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12077323 69110 Gata2 GATA binding protein 2 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21398579 69110 Gata2 GATA binding protein 2 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12689939 69110 Gata2 GATA binding protein 2 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 69110 Gata2 GATA binding protein 2 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:16543408 69110 Gata2 GATA binding protein 2 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20838598 69110 Gata2 GATA binding protein 2 gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19088086 69110 Gata2 GATA binding protein 2 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8078582 69110 Gata2 GATA binding protein 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18233958 69110 Gata2 GATA binding protein 2 gene MP:0003585 large ureter IAGP N RGD:5509061 20141003 MGI PMID:18233958 69110 Gata2 GATA binding protein 2 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:18233958 69110 Gata2 GATA binding protein 2 gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141003 MGI PMID:16543408 69110 Gata2 GATA binding protein 2 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220512 MGI PMID:27783953 69110 Gata2 GATA binding protein 2 gene MP:0003877 abnormal serotonergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19088086 69110 Gata2 GATA binding protein 2 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20221103 MGI 69110 Gata2 GATA binding protein 2 gene MP:0004727 absent epididymis IEA N RGD:5509061 20210128 MGI 69110 Gata2 GATA binding protein 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 69110 Gata2 GATA binding protein 2 gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20220512 MGI PMID:27783953 69110 Gata2 GATA binding protein 2 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:16543408 69110 Gata2 GATA binding protein 2 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 69110 Gata2 GATA binding protein 2 gene MP:0005119 decreased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:16543408 69110 Gata2 GATA binding protein 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18233958 69110 Gata2 GATA binding protein 2 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21398579 69110 Gata2 GATA binding protein 2 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20838598 69110 Gata2 GATA binding protein 2 gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20220512 MGI PMID:27783953 69110 Gata2 GATA binding protein 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19088086 69110 Gata2 GATA binding protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18233958 69110 Gata2 GATA binding protein 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18233958 69110 Gata2 GATA binding protein 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12077323 69110 Gata2 GATA binding protein 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16543408 69110 Gata2 GATA binding protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12689939 69110 Gata2 GATA binding protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16461905 69110 Gata2 GATA binding protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8078582 69110 Gata2 GATA binding protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 69110 Gata2 GATA binding protein 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18233958 69110 Gata2 GATA binding protein 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 69110 Gata2 GATA binding protein 2 gene MP:0031276 abnormal stress erythropoiesis IAGP N RGD:5509061 20210805 MGI PMID:20838598 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:23716600 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0003808 increased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0003922 abnormal heart right atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0003923 abnormal heart left atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18391014 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18391014 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0005337 abnormal retroperitoneal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18391014 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0006044 tricuspid valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0006048 pulmonary valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18391014 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18391014 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0008726 increased heart left atrium size IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0008727 increased heart right atrium size IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18391014 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0008817 hematoma IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0009287 decreased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20231221 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18391014 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0010127 hypervolemia IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0010563 increased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0010595 abnormal aortic valve cusp morphology IAGP N RGD:5509061 20231221 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0010695 abnormal blood pressure regulation IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18391014 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23716600 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23716600 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23874215 69111 Klf3 Kruppel-like transcription factor 3 (basic) gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23716600 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21803180 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16606348 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16606348 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16606348 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:16606348 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20210610 MGI PMID:33773101 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0003439 abnormal glycerol level IAGP N RGD:5509061 20141003 MGI PMID:16606348 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:21803180 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0004983 abnormal osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:21803180 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16606348 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:16606348 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210610 MGI PMID:33773101 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0005390 skeleton phenotype IAGP N RGD:5509061 20210610 MGI PMID:33773101 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20210610 MGI PMID:33773101 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16606348 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20210610 MGI PMID:33773101 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21803180 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0009345 abnormal trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:21803180 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16606348 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:16606348 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0010768 mortality/aging IAGP N RGD:5509061 20210610 MGI PMID:33773101 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0010874 abnormal bone volume IAGP N RGD:5509061 20141003 MGI PMID:21803180 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0010877 abnormal trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:21803180 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210610 MGI PMID:33773101 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:16606348 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20210610 MGI PMID:33773101 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0030674 decreased circulating alanine level IAGP N RGD:5509061 20180920 MGI PMID:16606348 69114 Pdk4 pyruvate dehydrogenase kinase, isoenzyme 4 gene MP:0030970 ketosis IAGP N RGD:5509061 20190815 MGI PMID:16606348 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15469964 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:10079221 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:10417393 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9744866 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000275 heart hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10417393 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10079221 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11565035 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16678773 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20180503 MGI PMID:27196371 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:16322092 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000635 pituitary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000636 enlarged pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000636 enlarged pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:9744866 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:9744866 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11134518 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16391232 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16537495 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9744866 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16537495 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11134518 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16537495 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:11134518 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:16391232 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:16537495 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:9744866 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8646780 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000840 abnormal epithalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:19147535 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220407 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:11134518 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:9744866 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001149 testicular hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11134518 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11565035 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15469964 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16014817 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16391232 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:8646780 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15685168 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:9744866 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:10079221 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:16391232 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:16537495 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11742404 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:11134518 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9744866 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:9744866 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:15685168 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:15685168 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15685168 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180503 MGI PMID:27196371 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20180503 MGI PMID:27196371 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23079656 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:19147535 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11134518 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8646780 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:20676139 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:11134518 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0001999 photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:15111307 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14647411 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19147535 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14647411 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14998493 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14647411 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19147535 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9744866 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11134518 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9744866 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16537495 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15685168 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16537495 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19147535 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20676139 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002083 premature death IAGP N RGD:5509061 20161222 MGI PMID:27354067 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:23028343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:15154924 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:15469964 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:16322092 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15469964 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:11134518 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:8646780 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:16014817 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:10417393 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:11565035 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:21194982 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20230608 MGI PMID:33594717 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0003496 increased thyroid adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20676139 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0003498 thyroid gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20676139 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20161222 MGI PMID:27354067 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:10417393 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:16014817 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:16014817 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:15685168 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19147535 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:12466968 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230608 MGI PMID:33594717 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10079221 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:15469964 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:15469964 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10079221 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10079221 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004407 increased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10079221 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004498 increased organ of Corti supporting cell number IAGP N RGD:5509061 20141003 MGI PMID:10079221 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16391232 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16391232 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:10417393 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004832 enlarged ovary IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:16014817 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:8646780 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:8646780 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0004958 enlarged prostate gland IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23079656 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11565035 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11742404 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23079656 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:16322092 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15469964 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:15685168 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15469964 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15469964 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:15685168 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15685168 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:16705040 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8646781 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19147535 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0006321 increased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:10417393 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:10079221 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20161222 MGI PMID:27354067 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0008105 increased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:16322092 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0008130 abnormal pituitary intermediate lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0008130 abnormal pituitary intermediate lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:9744866 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0008301 adrenal medulla hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0008371 pituitary intermediate lobe hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0008371 pituitary intermediate lobe hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8646780 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0008371 pituitary intermediate lobe hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9744866 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16322092 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0008939 increased pituitary gland weight IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:8646780 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20141003 MGI PMID:8646780 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0009130 increased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:15469964 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:15685168 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:15111307 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23079656 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15469964 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0009300 increased parametrial fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15469964 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0009381 abnormal prostate gland dorsolateral lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:16014817 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11565035 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16705040 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15469964 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0010236 abnormal retina outer limiting membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19147535 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16537495 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9744866 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0010321 increased parathyroid gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19261681 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20676139 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20230608 MGI PMID:33594717 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10557343 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11742404 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17409423 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19325126 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180503 MGI PMID:27196371 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16678773 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0011130 absent tertiary ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:8646779 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:15469964 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:10079221 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19147535 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0013539 increased ovary adenoma incidence IAGP N RGD:5509061 20161222 MGI PMID:27354067 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:33594717 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:14647411 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:9744866 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0030516 abnormal junctional epithelium morphology IAGP N RGD:5509061 20180111 MGI PMID:15154924 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0031359 decreased prostate gland anterior lobe weight IAGP N RGD:5509061 20220303 MGI PMID:16014817 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0031362 decreased prostate gland ventral lobe weight IAGP N RGD:5509061 20220303 MGI PMID:16014817 69116 Cdkn1b cyclin dependent kinase inhibitor 1B gene MP:0031366 decreased prostate gland dorsolateral lobe weight IAGP N RGD:5509061 20220303 MGI PMID:16014817 69118 Atrn attractin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11444801 69118 Atrn attractin gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11444801 69118 Atrn attractin gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:11444801 69118 Atrn attractin gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20141003 MGI PMID:11444801 69118 Atrn attractin gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:11444801 69118 Atrn attractin gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:18064672 69118 Atrn attractin gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141218 MGI PMID:18821597 69118 Atrn attractin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11444801 69118 Atrn attractin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11514456 69118 Atrn attractin gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11444801 69118 Atrn attractin gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11514456 69118 Atrn attractin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11444801 69118 Atrn attractin gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 69118 Atrn attractin gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11209055 69118 Atrn attractin gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:11209055 69118 Atrn attractin gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:11444801 69118 Atrn attractin gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 69118 Atrn attractin gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:12560552 69118 Atrn attractin gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11444801 69118 Atrn attractin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:12560552 69118 Atrn attractin gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:18064672 69118 Atrn attractin gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:11431694 69118 Atrn attractin gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:11444801 69118 Atrn attractin gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:12560552 69118 Atrn attractin gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:18064672 69118 Atrn attractin gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141218 MGI PMID:18821597 69118 Atrn attractin gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 69118 Atrn attractin gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:11444801 69118 Atrn attractin gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:11514456 69118 Atrn attractin gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:12560552 69118 Atrn attractin gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:18064672 69118 Atrn attractin gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141218 MGI PMID:18821597 69118 Atrn attractin gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:11444801 69118 Atrn attractin gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:11444801 69118 Atrn attractin gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11514456 69118 Atrn attractin gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 69118 Atrn attractin gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20181227 MGI 69118 Atrn attractin gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:11514456 69124 Lep leptin gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10359811 69124 Lep leptin gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16804058 69124 Lep leptin gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:10660043 69124 Lep leptin gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:16039170 69124 Lep leptin gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11445560 69124 Lep leptin gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177042 69124 Lep leptin gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 69124 Lep leptin gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177042 69124 Lep leptin gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 69124 Lep leptin gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12126735 69124 Lep leptin gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15319454 69124 Lep leptin gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15319454 69124 Lep leptin gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 69124 Lep leptin gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17873059 69124 Lep leptin gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:4588246 69124 Lep leptin gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:4588246 69124 Lep leptin gene MP:0000231 hypertension IAGP N RGD:5509061 20170209 MGI PMID:18160459 69124 Lep leptin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12885755 69124 Lep leptin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16394172 69124 Lep leptin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16612592 69124 Lep leptin gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20150514 MGI PMID:24680679 69124 Lep leptin gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17023554 69124 Lep leptin gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:16455789 69124 Lep leptin gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:16804058 69124 Lep leptin gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17003330 69124 Lep leptin gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0001142 abnormal vagina orifice morphology IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20220714 MGI PMID:12000791 69124 Lep leptin gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17130477 69124 Lep leptin gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0001257 increased body length IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:14824537 69124 Lep leptin gene MP:0001258 decreased body length IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:10742101 69124 Lep leptin gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:14578285 69124 Lep leptin gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:17873059 69124 Lep leptin gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:18682832 69124 Lep leptin gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:7560100 69124 Lep leptin gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:7800681 69124 Lep leptin gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:9623983 69124 Lep leptin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12897241 69124 Lep leptin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16804058 69124 Lep leptin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16879220 69124 Lep leptin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20368432 69124 Lep leptin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23684624 69124 Lep leptin gene MP:0001260 increased body weight IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0001260 increased body weight IAGP N RGD:5509061 20161103 MGI PMID:26074075 69124 Lep leptin gene MP:0001260 increased body weight IAGP N RGD:5509061 20170413 MGI PMID:25116704 69124 Lep leptin gene MP:0001260 increased body weight IAGP N RGD:5509061 20190905 MGI PMID:22118645 69124 Lep leptin gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12136396 69124 Lep leptin gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12540600 69124 Lep leptin gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12885755 69124 Lep leptin gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12925742 69124 Lep leptin gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:14978271 69124 Lep leptin gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15201286 69124 Lep leptin gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:16394172 69124 Lep leptin gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:19917283 69124 Lep leptin gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:9623983 69124 Lep leptin gene MP:0001261 obese IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0001261 obese IAGP N RGD:5509061 20170209 MGI PMID:18160459 69124 Lep leptin gene MP:0001261 obese IAGP N RGD:5509061 20170413 MGI PMID:25116704 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10742101 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12126735 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12244109 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12447443 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15064421 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16407534 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17003330 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19883618 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21298050 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21969596 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22232663 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22541436 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23238296 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141009 MGI PMID:24361012 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150101 MGI PMID:21897366 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160218 MGI PMID:24519944 69124 Lep leptin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210708 MGI PMID:33691105 69124 Lep leptin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16469807 69124 Lep leptin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22232663 69124 Lep leptin gene MP:0001263 weight loss IAGP N RGD:5509061 20141009 MGI PMID:24361012 69124 Lep leptin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10742101 69124 Lep leptin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19289822 69124 Lep leptin gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16998795 69124 Lep leptin gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20231207 MGI 69124 Lep leptin gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:16407534 69124 Lep leptin gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12897241 69124 Lep leptin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16293682 69124 Lep leptin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17550780 69124 Lep leptin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210826 MGI 69124 Lep leptin gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:19289822 69124 Lep leptin gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22232663 69124 Lep leptin gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:12244109 69124 Lep leptin gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:17003330 69124 Lep leptin gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:17550780 69124 Lep leptin gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:9623983 69124 Lep leptin gene MP:0001433 polyphagia IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:16293682 69124 Lep leptin gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200402 MGI 69124 Lep leptin gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16246967 69124 Lep leptin gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:11445560 69124 Lep leptin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11445560 69124 Lep leptin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16280642 69124 Lep leptin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16394172 69124 Lep leptin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16879220 69124 Lep leptin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17003330 69124 Lep leptin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18941143 69124 Lep leptin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23238296 69124 Lep leptin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:8177042 69124 Lep leptin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170209 MGI PMID:18160459 69124 Lep leptin gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20171102 MGI PMID:26880786 69124 Lep leptin gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12244109 69124 Lep leptin gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15319454 69124 Lep leptin gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16879220 69124 Lep leptin gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20170209 MGI PMID:18160459 69124 Lep leptin gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20190905 MGI PMID:22118645 69124 Lep leptin gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11445560 69124 Lep leptin gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12126735 69124 Lep leptin gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177042 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:11078464 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12136396 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15201286 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16280642 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17550780 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:18654634 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19917283 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:23238296 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:4588246 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141009 MGI PMID:24361012 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20170119 MGI PMID:27573812 69124 Lep leptin gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20170209 MGI PMID:18160459 69124 Lep leptin gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17023554 69124 Lep leptin gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:22232663 69124 Lep leptin gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:508700 69124 Lep leptin gene MP:0001744 hypersecretion of corticosterone IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:10660043 69124 Lep leptin gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:22958918 69124 Lep leptin gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:4588246 69124 Lep leptin gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:19289822 69124 Lep leptin gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:4588246 69124 Lep leptin gene MP:0001781 abnormal white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17003330 69124 Lep leptin gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23238296 69124 Lep leptin gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20160218 MGI PMID:24519944 69124 Lep leptin gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:17023554 69124 Lep leptin gene MP:0001860 liver inflammation IAGP N RGD:5509061 20190905 MGI PMID:22118645 69124 Lep leptin gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:16373670 69124 Lep leptin gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:22232663 69124 Lep leptin gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17550780 69124 Lep leptin gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0001924 infertility IAGP N RGD:5509061 20170413 MGI PMID:25116704 69124 Lep leptin gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0001925 male infertility IAGP N RGD:5509061 20170413 MGI PMID:25116704 69124 Lep leptin gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17550780 69124 Lep leptin gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:22232663 69124 Lep leptin gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0001926 female infertility IAGP N RGD:5509061 20170413 MGI PMID:25116704 69124 Lep leptin gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:19620723 69124 Lep leptin gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:17130477 69124 Lep leptin gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12244109 69124 Lep leptin gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12897241 69124 Lep leptin gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15201286 69124 Lep leptin gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16804058 69124 Lep leptin gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17003330 69124 Lep leptin gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11078464 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11481248 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12136396 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12540600 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12897241 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15201286 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16280642 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16394172 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16879220 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17003330 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17550780 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19103808 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19883618 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:4588246 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141009 MGI PMID:24361012 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20170209 MGI PMID:18160459 69124 Lep leptin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20171102 MGI PMID:26880786 69124 Lep leptin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23238296 69124 Lep leptin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:4588246 69124 Lep leptin gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19528970 69124 Lep leptin gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:10660043 69124 Lep leptin gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12244109 69124 Lep leptin gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15319454 69124 Lep leptin gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19883618 69124 Lep leptin gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:16407534 69124 Lep leptin gene MP:0002164 abnormal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16804058 69124 Lep leptin gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23864684 69124 Lep leptin gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:22958920 69124 Lep leptin gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:17023554 69124 Lep leptin gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12885755 69124 Lep leptin gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12897241 69124 Lep leptin gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17003330 69124 Lep leptin gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17482547 69124 Lep leptin gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:22958918 69124 Lep leptin gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23238296 69124 Lep leptin gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20190905 MGI PMID:22118645 69124 Lep leptin gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16804058 69124 Lep leptin gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18682832 69124 Lep leptin gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18941143 69124 Lep leptin gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12126735 69124 Lep leptin gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18682832 69124 Lep leptin gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10359811 69124 Lep leptin gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12244109 69124 Lep leptin gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12447443 69124 Lep leptin gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15319454 69124 Lep leptin gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16804058 69124 Lep leptin gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16879220 69124 Lep leptin gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18654634 69124 Lep leptin gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19289822 69124 Lep leptin gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21998599 69124 Lep leptin gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141009 MGI PMID:24361012 69124 Lep leptin gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20190502 MGI 69124 Lep leptin gene MP:0002764 short tibia IEA N RGD:5509061 20190502 MGI 69124 Lep leptin gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20170413 MGI PMID:25116704 69124 Lep leptin gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20170413 MGI PMID:25116704 69124 Lep leptin gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15331557 69124 Lep leptin gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:16246967 69124 Lep leptin gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0002834 decreased heart weight IEA N RGD:5509061 20200402 MGI 69124 Lep leptin gene MP:0002865 increased growth rate IAGP N RGD:5509061 20141003 MGI PMID:14824537 69124 Lep leptin gene MP:0002865 increased growth rate IAGP N RGD:5509061 20141003 MGI PMID:4588246 69124 Lep leptin gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15064421 69124 Lep leptin gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12540600 69124 Lep leptin gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16804058 69124 Lep leptin gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:18682832 69124 Lep leptin gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20150101 MGI PMID:21897366 69124 Lep leptin gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15064421 69124 Lep leptin gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:19917283 69124 Lep leptin gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15064421 69124 Lep leptin gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20191128 MGI PMID:29551634 69124 Lep leptin gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17003330 69124 Lep leptin gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0002981 increased liver weight IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16039170 69124 Lep leptin gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19103808 69124 Lep leptin gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19103808 69124 Lep leptin gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141009 MGI PMID:24361012 69124 Lep leptin gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20161201 MGI PMID:25621497 69124 Lep leptin gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:16039170 69124 Lep leptin gene MP:0003177 allodynia IAGP N RGD:5509061 20141003 MGI PMID:19620723 69124 Lep leptin gene MP:0003194 abnormal frequency of paradoxical sleep IAGP N RGD:5509061 20141003 MGI PMID:16293682 69124 Lep leptin gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20190905 MGI PMID:22118645 69124 Lep leptin gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:11078464 69124 Lep leptin gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:12136396 69124 Lep leptin gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:19289822 69124 Lep leptin gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:16804058 69124 Lep leptin gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:19289822 69124 Lep leptin gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19883618 69124 Lep leptin gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:21298050 69124 Lep leptin gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20240627 MGI PMID:38626531 69124 Lep leptin gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:4588246 69124 Lep leptin gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:7835283 69124 Lep leptin gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:8360782 69124 Lep leptin gene MP:0003619 abnormal urine color IAGP N RGD:5509061 20141003 MGI PMID:23238296 69124 Lep leptin gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:12136396 69124 Lep leptin gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141009 MGI PMID:24361012 69124 Lep leptin gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:16039170 69124 Lep leptin gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0003674 oxidative stress IAGP N RGD:5509061 20161201 MGI PMID:25621497 69124 Lep leptin gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12107823 69124 Lep leptin gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20210128 MGI 69124 Lep leptin gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20191128 MGI PMID:29551634 69124 Lep leptin gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20190905 MGI PMID:22118645 69124 Lep leptin gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20190418 MGI PMID:21554665 69124 Lep leptin gene MP:0003956 abnormal body size IAGP N RGD:5509061 20141003 MGI PMID:14578285 69124 Lep leptin gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17550780 69124 Lep leptin gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20161103 MGI PMID:26074075 69124 Lep leptin gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20190418 MGI PMID:21554665 69124 Lep leptin gene MP:0003972 decreased pituitary hormone level IAGP N RGD:5509061 20170413 MGI PMID:25116704 69124 Lep leptin gene MP:0003973 increased pituitary hormone level IAGP N RGD:5509061 20170413 MGI PMID:25116704 69124 Lep leptin gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20190905 MGI PMID:22118645 69124 Lep leptin gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0004112 abnormal arteriole morphology IAGP N RGD:5509061 20141003 MGI PMID:19502550 69124 Lep leptin gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:19103808 69124 Lep leptin gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:16394172 69124 Lep leptin gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16282354 69124 Lep leptin gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:16039170 69124 Lep leptin gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:16394172 69124 Lep leptin gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:16039170 69124 Lep leptin gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:19528970 69124 Lep leptin gene MP:0004847 abnormal liver weight IAGP N RGD:5509061 20141003 MGI PMID:7815168 69124 Lep leptin gene MP:0004848 abnormal liver size IAGP N RGD:5509061 20141003 MGI PMID:14578285 69124 Lep leptin gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:17095713 69124 Lep leptin gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:23684624 69124 Lep leptin gene MP:0004909 increased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:16549076 69124 Lep leptin gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220811 MGI 69124 Lep leptin gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20068132 69124 Lep leptin gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20170413 MGI PMID:25116704 69124 Lep leptin gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20170413 MGI PMID:25116704 69124 Lep leptin gene MP:0005129 increased adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0005129 increased adrenocorticotropin level IAGP N RGD:5509061 20190418 MGI PMID:21554665 69124 Lep leptin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16394172 69124 Lep leptin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16612592 69124 Lep leptin gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15319454 69124 Lep leptin gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177042 69124 Lep leptin gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 69124 Lep leptin gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11445560 69124 Lep leptin gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12126735 69124 Lep leptin gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16879220 69124 Lep leptin gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177042 69124 Lep leptin gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 69124 Lep leptin gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20171102 MGI PMID:26880786 69124 Lep leptin gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15319454 69124 Lep leptin gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16804058 69124 Lep leptin gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19883618 69124 Lep leptin gene MP:0005180 abnormal circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:12136396 69124 Lep leptin gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:16280642 69124 Lep leptin gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:10359811 69124 Lep leptin gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:14578285 69124 Lep leptin gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16804058 69124 Lep leptin gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:12244109 69124 Lep leptin gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:7800681 69124 Lep leptin gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:7815168 69124 Lep leptin gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:12897241 69124 Lep leptin gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:16469807 69124 Lep leptin gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:7815168 69124 Lep leptin gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20150101 MGI PMID:21897366 69124 Lep leptin gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:23684624 69124 Lep leptin gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:7815168 69124 Lep leptin gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12897241 69124 Lep leptin gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12540600 69124 Lep leptin gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16804058 69124 Lep leptin gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18682832 69124 Lep leptin gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19103808 69124 Lep leptin gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22232663 69124 Lep leptin gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22541436 69124 Lep leptin gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141009 MGI PMID:24361012 69124 Lep leptin gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20150101 MGI PMID:21897366 69124 Lep leptin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11481248 69124 Lep leptin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:14578285 69124 Lep leptin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15319454 69124 Lep leptin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16280642 69124 Lep leptin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16326714 69124 Lep leptin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16394172 69124 Lep leptin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18654634 69124 Lep leptin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22958918 69124 Lep leptin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23684624 69124 Lep leptin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20161103 MGI PMID:26074075 69124 Lep leptin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20170209 MGI PMID:18160459 69124 Lep leptin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210708 MGI PMID:33691105 69124 Lep leptin gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12126735 69124 Lep leptin gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12244109 69124 Lep leptin gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:12930764 69124 Lep leptin gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15319454 69124 Lep leptin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:16280642 69124 Lep leptin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:16394172 69124 Lep leptin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17003330 69124 Lep leptin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22958918 69124 Lep leptin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23238296 69124 Lep leptin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20171102 MGI PMID:26880786 69124 Lep leptin gene MP:0005333 decreased heart rate IEA N RGD:5509061 20200402 MGI 69124 Lep leptin gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:10742101 69124 Lep leptin gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17003330 69124 Lep leptin gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18682832 69124 Lep leptin gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:11445560 69124 Lep leptin gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20170209 MGI PMID:18160459 69124 Lep leptin gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:12897241 69124 Lep leptin gene MP:0005407 hyperalgesia IAGP N RGD:5509061 20141003 MGI PMID:19620723 69124 Lep leptin gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16804058 69124 Lep leptin gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:14578285 69124 Lep leptin gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:17550780 69124 Lep leptin gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:12244109 69124 Lep leptin gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12897241 69124 Lep leptin gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18682832 69124 Lep leptin gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:23684624 69124 Lep leptin gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17482547 69124 Lep leptin gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17550780 69124 Lep leptin gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11078464 69124 Lep leptin gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:16469807 69124 Lep leptin gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:22232663 69124 Lep leptin gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:840297 69124 Lep leptin gene MP:0005535 abnormal body temperature IAGP N RGD:5509061 20141003 MGI PMID:14578285 69124 Lep leptin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15319454 69124 Lep leptin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16879220 69124 Lep leptin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17003330 69124 Lep leptin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17482547 69124 Lep leptin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19289822 69124 Lep leptin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19883618 69124 Lep leptin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21998599 69124 Lep leptin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22958918 69124 Lep leptin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23238296 69124 Lep leptin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23684624 69124 Lep leptin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141009 MGI PMID:24361012 69124 Lep leptin gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20171102 MGI PMID:26880786 69124 Lep leptin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12126735 69124 Lep leptin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12447443 69124 Lep leptin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12540600 69124 Lep leptin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12897241 69124 Lep leptin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16407534 69124 Lep leptin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16804058 69124 Lep leptin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16879220 69124 Lep leptin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17068142 69124 Lep leptin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19103808 69124 Lep leptin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141009 MGI PMID:24361012 69124 Lep leptin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20161208 MGI PMID:22958920 69124 Lep leptin gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:10660043 69124 Lep leptin gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:14978271 69124 Lep leptin gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:23684624 69124 Lep leptin gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12355168 69124 Lep leptin gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20190905 MGI PMID:22118645 69124 Lep leptin gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15319454 69124 Lep leptin gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20191128 MGI PMID:29551634 69124 Lep leptin gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20170413 MGI PMID:25116704 69124 Lep leptin gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:1013161 69124 Lep leptin gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:16879220 69124 Lep leptin gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22958920 69124 Lep leptin gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:7815168 69124 Lep leptin gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20240627 MGI PMID:38626531 69124 Lep leptin gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:16998795 69124 Lep leptin gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20068132 69124 Lep leptin gene MP:0008329 decreased somatotroph cell number IAGP N RGD:5509061 20170413 MGI PMID:25116704 69124 Lep leptin gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:10660043 69124 Lep leptin gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16282354 69124 Lep leptin gene MP:0008459 abnormal circulating pancreatic peptide level IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20141003 MGI PMID:7800681 69124 Lep leptin gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:12107823 69124 Lep leptin gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17023554 69124 Lep leptin gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17023554 69124 Lep leptin gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17023554 69124 Lep leptin gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:11481248 69124 Lep leptin gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:17130477 69124 Lep leptin gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20160218 MGI PMID:24519944 69124 Lep leptin gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23684624 69124 Lep leptin gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:9623983 69124 Lep leptin gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22232663 69124 Lep leptin gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:23684624 69124 Lep leptin gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20141003 MGI PMID:12000791 69124 Lep leptin gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141009 MGI PMID:24361012 69124 Lep leptin gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:16280642 69124 Lep leptin gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:19289822 69124 Lep leptin gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141009 MGI PMID:24361012 69124 Lep leptin gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20180614 MGI PMID:18654634 69124 Lep leptin gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15319454 69124 Lep leptin gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:5059196 69124 Lep leptin gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23238296 69124 Lep leptin gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0009130 increased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20160407 MGI PMID:7815168 69124 Lep leptin gene MP:0009167 increased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:4588246 69124 Lep leptin gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:16280642 69124 Lep leptin gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:4588246 69124 Lep leptin gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:19289822 69124 Lep leptin gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:11078464 69124 Lep leptin gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:17003330 69124 Lep leptin gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21969596 69124 Lep leptin gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21298050 69124 Lep leptin gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10742101 69124 Lep leptin gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21969596 69124 Lep leptin gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:7815168 69124 Lep leptin gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10742101 69124 Lep leptin gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12453895 69124 Lep leptin gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21298050 69124 Lep leptin gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:20068132 69124 Lep leptin gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23684624 69124 Lep leptin gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11445560 69124 Lep leptin gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22958918 69124 Lep leptin gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23864684 69124 Lep leptin gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20171102 MGI PMID:26880786 69124 Lep leptin gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15319454 69124 Lep leptin gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16804058 69124 Lep leptin gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19883618 69124 Lep leptin gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23238296 69124 Lep leptin gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23864684 69124 Lep leptin gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:19528970 69124 Lep leptin gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:19528970 69124 Lep leptin gene MP:0009436 fragmentation of sleep/wake states IAGP N RGD:5509061 20141003 MGI PMID:16293682 69124 Lep leptin gene MP:0009536 abnormal interstitial cell of Cajal morphology IAGP N RGD:5509061 20141003 MGI PMID:19917283 69124 Lep leptin gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:1382044 69124 Lep leptin gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22232663 69124 Lep leptin gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:14978271 69124 Lep leptin gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21151569 69124 Lep leptin gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20161103 MGI PMID:26074075 69124 Lep leptin gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15319454 69124 Lep leptin gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11445560 69124 Lep leptin gene MP:0010053 decreased grip strength IEA N RGD:5509061 20190502 MGI 69124 Lep leptin gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20161201 MGI PMID:25621497 69124 Lep leptin gene MP:0010143 enhanced fertility IAGP N RGD:5509061 20141003 MGI PMID:22232663 69124 Lep leptin gene MP:0010143 enhanced fertility IAGP N RGD:5509061 20220714 MGI PMID:12000791 69124 Lep leptin gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:23238296 69124 Lep leptin gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:16469807 69124 Lep leptin gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20150101 MGI PMID:21897366 69124 Lep leptin gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20210128 MGI 69124 Lep leptin gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:15319454 69124 Lep leptin gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:16246967 69124 Lep leptin gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:17550780 69124 Lep leptin gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:12897241 69124 Lep leptin gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:16469807 69124 Lep leptin gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:6393185 69124 Lep leptin gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:840297 69124 Lep leptin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:12000791 69124 Lep leptin gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20141003 MGI PMID:23238296 69124 Lep leptin gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:20634301 69124 Lep leptin gene MP:0011478 abnormal urine catecholamine level IAGP N RGD:5509061 20141003 MGI PMID:1382044 69124 Lep leptin gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:12897241 69124 Lep leptin gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:15064421 69124 Lep leptin gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:16469807 69124 Lep leptin gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:15064421 69124 Lep leptin gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:23238296 69124 Lep leptin gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:7560100 69124 Lep leptin gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:17465682 69124 Lep leptin gene MP:0011951 increased cardiac stroke volume IEA N RGD:5509061 20210128 MGI 69124 Lep leptin gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20220811 MGI 69124 Lep leptin gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20220811 MGI 69124 Lep leptin gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 69124 Lep leptin gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:16282354 69124 Lep leptin gene MP:0012706 decreased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16282354 69124 Lep leptin gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20151015 MGI PMID:25144618 69124 Lep leptin gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:16455789 69124 Lep leptin gene MP:0014142 increased body fat mass IEA N RGD:5509061 20160407 MGI 69124 Lep leptin gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20160407 MGI PMID:17003330 69124 Lep leptin gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20210708 MGI PMID:33691105 69124 Lep leptin gene MP:0014174 decreased fatty acid beta-oxidation IAGP N RGD:5509061 20160421 MGI PMID:22958918 69124 Lep leptin gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:16804058 69124 Lep leptin gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:16804058 69124 Lep leptin gene MP:0030603 increased sperm number IAGP N RGD:5509061 20220714 MGI PMID:12000791 69124 Lep leptin gene MP:0030770 increased urine adrenaline level IAGP N RGD:5509061 20180927 MGI PMID:23684624 69124 Lep leptin gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:17003330 69124 Lep leptin gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:17465682 69124 Lep leptin gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:22118645 69124 Lep leptin gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:15319454 69124 Lep leptin gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:12000791 69124 Lep leptin gene MP:0031417 decreased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:23423172 69127 Ccl5 C-C motif chemokine ligand 5 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11890717 69127 Ccl5 C-C motif chemokine ligand 5 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11890717 69127 Ccl5 C-C motif chemokine ligand 5 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11890717 69127 Ccl5 C-C motif chemokine ligand 5 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11890717 69127 Ccl5 C-C motif chemokine ligand 5 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:11890717 69131 Gckr glucokinase regulatory protein gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10588736 69131 Gckr glucokinase regulatory protein gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10588736 69131 Gckr glucokinase regulatory protein gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10713097 69131 Gckr glucokinase regulatory protein gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:10588736 69131 Gckr glucokinase regulatory protein gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:10713097 69131 Gckr glucokinase regulatory protein gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:10588736 69131 Gckr glucokinase regulatory protein gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:10713097 69131 Gckr glucokinase regulatory protein gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:10588736 69131 Gckr glucokinase regulatory protein gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 69131 Gckr glucokinase regulatory protein gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10588736 69131 Gckr glucokinase regulatory protein gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 69131 Gckr glucokinase regulatory protein gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:10588736 69131 Gckr glucokinase regulatory protein gene MP:0011606 decreased glucokinase activity IAGP N RGD:5509061 20141003 MGI PMID:10588736 69131 Gckr glucokinase regulatory protein gene MP:0011606 decreased glucokinase activity IAGP N RGD:5509061 20141003 MGI PMID:10713097 69135 Osm oncostatin M gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210520 MGI 69135 Osm oncostatin M gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:14985435 69135 Osm oncostatin M gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 69135 Osm oncostatin M gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20210128 MGI 69135 Osm oncostatin M gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 69135 Osm oncostatin M gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210520 MGI 69135 Osm oncostatin M gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210520 MGI 69135 Osm oncostatin M gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:14985435 69135 Osm oncostatin M gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210520 MGI 69135 Osm oncostatin M gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 69135 Osm oncostatin M gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 69135 Osm oncostatin M gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20181011 MGI 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:12932358 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12932358 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16301621 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12932358 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16301621 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:16301621 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0001806 decreased IgM level IEA N RGD:5509061 20181011 MGI 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0001844 autoimmune response IEA N RGD:5509061 20141003 MGI 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:12932358 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24336796 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24336796 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12932358 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16301621 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12932358 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0002494 increased IgM level IEA N RGD:5509061 20181011 MGI 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0002495 increased IgA level IEA N RGD:5509061 20181011 MGI 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:12932358 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:12932358 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:24336796 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:12932358 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:12932358 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12932358 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12932358 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16301621 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20181011 MGI 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12932358 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12932358 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0008037 abnormal T cell morphology IEA N RGD:5509061 20190103 MGI 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20181011 MGI 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24336796 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24336796 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:16301621 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:16301621 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20181011 MGI 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20181011 MGI 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20151126 MGI PMID:22719950 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20181011 MGI 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24336796 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 69138 Rasgrp1 RAS guanyl releasing protein 1 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 69141 Smad7 SMAD family member 7 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:23011393 69141 Smad7 SMAD family member 7 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:23011393 69141 Smad7 SMAD family member 7 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:20354004 69141 Smad7 SMAD family member 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16709837 69141 Smad7 SMAD family member 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23011393 69141 Smad7 SMAD family member 7 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23011393 69141 Smad7 SMAD family member 7 gene MP:0001830 decreased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:20354004 69141 Smad7 SMAD family member 7 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:16709837 69141 Smad7 SMAD family member 7 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141016 MGI PMID:23903754 69141 Smad7 SMAD family member 7 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23011393 69141 Smad7 SMAD family member 7 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:23603491 69141 Smad7 SMAD family member 7 gene MP:0003410 abnormal artery development IAGP N RGD:5509061 20141003 MGI PMID:23011393 69141 Smad7 SMAD family member 7 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23011393 69141 Smad7 SMAD family member 7 gene MP:0003898 abnormal QRS complex IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:20354004 69141 Smad7 SMAD family member 7 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:16709837 69141 Smad7 SMAD family member 7 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16709837 69141 Smad7 SMAD family member 7 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20354004 69141 Smad7 SMAD family member 7 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23011393 69141 Smad7 SMAD family member 7 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20354004 69141 Smad7 SMAD family member 7 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20354004 69141 Smad7 SMAD family member 7 gene MP:0008712 decreased interleukin-9 secretion IAGP N RGD:5509061 20141003 MGI PMID:20354004 69141 Smad7 SMAD family member 7 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16709837 69141 Smad7 SMAD family member 7 gene MP:0008837 increased transforming growth factor beta level IAGP N RGD:5509061 20141003 MGI PMID:20354004 69141 Smad7 SMAD family member 7 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23603491 69141 Smad7 SMAD family member 7 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:23603491 69141 Smad7 SMAD family member 7 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141016 MGI PMID:23903754 69141 Smad7 SMAD family member 7 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:16709837 69141 Smad7 SMAD family member 7 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23011393 69141 Smad7 SMAD family member 7 gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16709837 69141 Smad7 SMAD family member 7 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20354004 69141 Smad7 SMAD family member 7 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0021160 decreased heart right ventricle wall thickness IAGP N RGD:5509061 20231221 MGI PMID:18952608 69141 Smad7 SMAD family member 7 gene MP:0031510 increased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:23011393 69143 Mdk midkine gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:15482347 69143 Mdk midkine gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:10683378 69143 Mdk midkine gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:10096022 69143 Mdk midkine gene MP:0001127 small ovary IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0001140 abnormal vagina epithelium morphology IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0001142 abnormal vagina orifice morphology IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0001143 constricted vagina orifice IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:19217924 69143 Mdk midkine gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10096022 69143 Mdk midkine gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 69143 Mdk midkine gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210520 MGI 69143 Mdk midkine gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:15482347 69143 Mdk midkine gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16619002 69143 Mdk midkine gene MP:0001926 female infertility IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:16619002 69143 Mdk midkine gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:10096022 69143 Mdk midkine gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 69143 Mdk midkine gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0002704 tubular nephritis IAGP N RGD:5509061 20141003 MGI PMID:15509530 69143 Mdk midkine gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20210520 MGI 69143 Mdk midkine gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:15482347 69143 Mdk midkine gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:15509530 69143 Mdk midkine gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:15482347 69143 Mdk midkine gene MP:0004895 vagina atrophy IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:15047154 69143 Mdk midkine gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 69143 Mdk midkine gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 69143 Mdk midkine gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:19217924 69143 Mdk midkine gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10683378 69143 Mdk midkine gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15482347 69143 Mdk midkine gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0009014 prolonged proestrus IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0009018 short estrus IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:19217924 69143 Mdk midkine gene MP:0009708 vaginal septum IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15482347 69143 Mdk midkine gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20220120 MGI PMID:17121547 69143 Mdk midkine gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20231207 MGI 69143 Mdk midkine gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:17121547 69156 Timp4 tissue inhibitor of metalloproteinase 4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 69156 Timp4 tissue inhibitor of metalloproteinase 4 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:20516072 69156 Timp4 tissue inhibitor of metalloproteinase 4 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 69156 Timp4 tissue inhibitor of metalloproteinase 4 gene MP:0001333 absent optic nerve IEA N RGD:5509061 20201022 MGI 69156 Timp4 tissue inhibitor of metalloproteinase 4 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20200514 MGI 69156 Timp4 tissue inhibitor of metalloproteinase 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 69156 Timp4 tissue inhibitor of metalloproteinase 4 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 69156 Timp4 tissue inhibitor of metalloproteinase 4 gene MP:0003023 decreased coronary flow rate IAGP N RGD:5509061 20141003 MGI PMID:20516072 69156 Timp4 tissue inhibitor of metalloproteinase 4 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:20516072 69156 Timp4 tissue inhibitor of metalloproteinase 4 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20516072 69156 Timp4 tissue inhibitor of metalloproteinase 4 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:20516072 69156 Timp4 tissue inhibitor of metalloproteinase 4 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20516072 69156 Timp4 tissue inhibitor of metalloproteinase 4 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 69158 Btg2 BTG anti-proliferation factor 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 69158 Btg2 BTG anti-proliferation factor 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 69158 Btg2 BTG anti-proliferation factor 2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:15542835 69158 Btg2 BTG anti-proliferation factor 2 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:15542835 69158 Btg2 BTG anti-proliferation factor 2 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:15542835 69158 Btg2 BTG anti-proliferation factor 2 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20240523 MGI 69158 Btg2 BTG anti-proliferation factor 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 69158 Btg2 BTG anti-proliferation factor 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0000461 decreased presacral vertebrae number IEA N RGD:5509061 20111116 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0000480 increased rib number IEA N RGD:5509061 20111116 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:9362463 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20111116 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0000562 polydactyly IEA N RGD:5509061 20111116 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:7885472 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:9362463 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:9362463 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20141003 MGI PMID:9362463 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:9790192 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0001406 abnormal gait IEA N RGD:5509061 20141003 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0001513 limb grasping IEA N RGD:5509061 20141003 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:19023080 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19023080 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0001924 infertility IEA N RGD:5509061 20111116 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9790192 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:21508348 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9790192 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9362463 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:7885472 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9362463 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21508348 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:9790192 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0002674 abnormal sperm motility IEA N RGD:5509061 20141003 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0002765 short fibula IEA N RGD:5509061 20111116 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0003572 abnormal uterus development IAGP N RGD:5509061 20141003 MGI PMID:9790192 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20141003 MGI PMID:9790192 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0003826 abnormal Mullerian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:21490063 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0003826 abnormal Mullerian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:9790192 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0004342 scapular bone foramen IEA N RGD:5509061 20111116 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0004351 short humerus IEA N RGD:5509061 20141003 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0004360 absent ulna IAGP N RGD:5509061 20141003 MGI PMID:7885472 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0005108 abnormal ulna morphology IEA N RGD:5509061 20111116 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0005167 abnormal blood-brain barrier function IAGP N RGD:5509061 20141003 MGI PMID:19023080 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20141003 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19023080 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0006279 abnormal limb development IEA N RGD:5509061 20141003 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0008257 thin myometrium IAGP N RGD:5509061 20141003 MGI PMID:9790192 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0008730 fused phalanges IEA N RGD:5509061 20141003 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0008985 hemimelia IEA N RGD:5509061 20111116 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0009071 short oviduct IAGP N RGD:5509061 20141003 MGI PMID:9790192 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0009081 thin uterus IAGP N RGD:5509061 20141003 MGI PMID:9790192 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0009097 absent endometrial glands IAGP N RGD:5509061 20141003 MGI PMID:21508348 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0009097 absent endometrial glands IAGP N RGD:5509061 20141003 MGI PMID:9790192 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0009139 failure of Mullerian duct regression IAGP N RGD:5509061 20141003 MGI PMID:21490063 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0009139 failure of Mullerian duct regression IAGP N RGD:5509061 20141003 MGI PMID:9790192 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0009669 abnormal postimplantation uterine environment IAGP N RGD:5509061 20141003 MGI PMID:21508348 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0009931 abnormal skin appearance IEA N RGD:5509061 20141003 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9362463 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19023080 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20141003 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0014321 short forelimb IEA N RGD:5509061 20231130 MGI 69160 Wnt7a wingless-type MMTV integration site family, member 7A gene MP:0031336 abnormal uterine epithelium development IAGP N RGD:5509061 20220120 MGI PMID:9790192 69162 Nfix nuclear factor I/X gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:18477394 69162 Nfix nuclear factor I/X gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18477394 69162 Nfix nuclear factor I/X gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:18477394 69162 Nfix nuclear factor I/X gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:18477394 69162 Nfix nuclear factor I/X gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20201029 MGI PMID:30503862 69162 Nfix nuclear factor I/X gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18477394 69162 Nfix nuclear factor I/X gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:18477394 69162 Nfix nuclear factor I/X gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20201029 MGI PMID:30503862 69162 Nfix nuclear factor I/X gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:18477394 69162 Nfix nuclear factor I/X gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18477394 69162 Nfix nuclear factor I/X gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:18477394 69162 Nfix nuclear factor I/X gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20201029 MGI PMID:30503862 69162 Nfix nuclear factor I/X gene MP:0002729 abnormal inner ear canal morphology IAGP N RGD:5509061 20141003 MGI PMID:18477394 69162 Nfix nuclear factor I/X gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0004684 intervertebral disk degeneration IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0004874 abnormal timing of postnatal eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0005238 increased brain size IAGP N RGD:5509061 20201029 MGI PMID:30503862 69162 Nfix nuclear factor I/X gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0008221 abnormal hippocampal commissure morphology IAGP N RGD:5509061 20201029 MGI PMID:30503862 69162 Nfix nuclear factor I/X gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20201029 MGI PMID:30503862 69162 Nfix nuclear factor I/X gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:18477394 69162 Nfix nuclear factor I/X gene MP:0008431 abnormal short-term spatial reference memory IAGP N RGD:5509061 20201029 MGI PMID:30503862 69162 Nfix nuclear factor I/X gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20201029 MGI PMID:30503862 69162 Nfix nuclear factor I/X gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20201029 MGI PMID:30503862 69162 Nfix nuclear factor I/X gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18477394 69162 Nfix nuclear factor I/X gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:18477394 69162 Nfix nuclear factor I/X gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20201029 MGI PMID:30503862 69162 Nfix nuclear factor I/X gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17353270 69162 Nfix nuclear factor I/X gene MP:0012293 impaired active avoidance behavior IAGP N RGD:5509061 20201029 MGI PMID:30503862 69162 Nfix nuclear factor I/X gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20201029 MGI PMID:30503862 69162 Nfix nuclear factor I/X gene MP:0012473 increased cingulate cortex size IAGP N RGD:5509061 20201029 MGI PMID:30503862 69162 Nfix nuclear factor I/X gene MP:0012489 abnormal retrosplenial region morphology IAGP N RGD:5509061 20201029 MGI PMID:30503862 69162 Nfix nuclear factor I/X gene MP:0020067 increased neocortex size IAGP N RGD:5509061 20201029 MGI PMID:30503862 69162 Nfix nuclear factor I/X gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20201029 MGI PMID:30503862 69164 Ifrd1 interferon-related developmental regulator 1 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:15060170 69164 Ifrd1 interferon-related developmental regulator 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15060170 69164 Ifrd1 interferon-related developmental regulator 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15060170 69164 Ifrd1 interferon-related developmental regulator 1 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20240627 MGI PMID:37603466 69164 Ifrd1 interferon-related developmental regulator 1 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20240627 MGI PMID:37603466 69164 Ifrd1 interferon-related developmental regulator 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20240627 MGI PMID:37603466 69164 Ifrd1 interferon-related developmental regulator 1 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20240627 MGI PMID:37603466 69164 Ifrd1 interferon-related developmental regulator 1 gene MP:0009426 decreased soleus weight IAGP N RGD:5509061 20141003 MGI PMID:15060170 69164 Ifrd1 interferon-related developmental regulator 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20240627 MGI PMID:37603466 69164 Ifrd1 interferon-related developmental regulator 1 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20240627 MGI PMID:37603466 69164 Ifrd1 interferon-related developmental regulator 1 gene MP:0011169 abnormal white fat cell differentation IAGP N RGD:5509061 20240627 MGI PMID:37603466 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:15254591 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:15919792 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000168 abnormal bone marrow development IAGP N RGD:5509061 20141003 MGI PMID:15067317 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000175 absent bone marrow cell IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19666848 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:15254591 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18382765 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19801450 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10549290 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17652179 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:17652179 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:18382765 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:19801450 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:14660788 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:17652179 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000649 sebaceous gland atrophy IAGP N RGD:5509061 20141003 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19666848 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:15956187 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15249658 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19117549 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19666848 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19117549 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001490 abnormal vibrissae reflex IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001573 abnormal circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001599 abnormal blood volume IAGP N RGD:5509061 20141003 MGI PMID:15956187 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:19666848 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16051889 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:19117549 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:10549290 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:15070754 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10549290 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15231871 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17652179 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:14660788 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15070754 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001781 abnormal white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:14660788 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001781 abnormal white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15249658 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11884400 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11884400 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11884400 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21076077 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0001993 abnormal blinking IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10675354 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14536066 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15919792 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14660788 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11514592 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19997628 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11857800 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16751185 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:10549290 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:15067317 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11909955 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002596 abnormal hematocrit IAGP N RGD:5509061 20141003 MGI PMID:15956187 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:14660788 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14536066 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19117549 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:10549290 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:14536066 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:21076077 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17003451 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19884495 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19884495 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:10675354 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:14536066 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19117549 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15249658 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:14660788 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15249658 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20160414 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:19666848 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:19117549 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0003846 matted coat IAGP N RGD:5509061 20141003 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19666848 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15930296 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004560 abnormal chorionic plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10549290 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:16051889 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:19737866 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19439596 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19666848 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:17652179 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:15067317 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10549290 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10549290 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15067317 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19117549 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005114 premature hair loss IAGP N RGD:5509061 20141003 MGI PMID:17652179 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005133 increased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:21076077 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:11159886 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:11889020 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19117549 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:14536066 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15254591 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19117549 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15919792 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19884495 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19801450 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:14660788 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15249658 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16051889 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15254591 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15254591 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005346 abnormal circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:15956187 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:15070754 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:14517292 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15919792 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:15070754 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:14536066 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15249658 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15919792 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:15249658 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:15919792 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0006080 brain ischemia IAGP N RGD:5509061 20141003 MGI PMID:19439596 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:19117549 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20170119 MGI PMID:15919792 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:11884400 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0006274 abnormal urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:15956187 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0006320 abnormal interscapular fat pad morphology IAGP N RGD:5509061 20191017 MGI PMID:31435015 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008244 abnormal peritoneal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15067317 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:15067317 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:20519122 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:14660788 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008541 leukostasis IAGP N RGD:5509061 20141003 MGI PMID:17003451 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10549290 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10549290 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20141003 MGI PMID:17652179 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008861 abnormal hair shedding IAGP N RGD:5509061 20141003 MGI PMID:17652179 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15956187 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19117549 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20141003 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009010 abnormal diestrus IAGP N RGD:5509061 20141003 MGI PMID:21076077 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009110 pancreas hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15067317 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15254591 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18204460 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15070754 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15070754 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:14660788 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009119 increased brown fat cell size IAGP N RGD:5509061 20141003 MGI PMID:14660788 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009119 increased brown fat cell size IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:15070754 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:15249658 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009128 decreased brown fat cell number IAGP N RGD:5509061 20141003 MGI PMID:14660788 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:15249658 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009132 abnormal white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:15249658 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009135 abnormal brown fat cell size IAGP N RGD:5509061 20141003 MGI PMID:14660788 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009137 decreased brown fat lipid droplet number IAGP N RGD:5509061 20141003 MGI PMID:15249658 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009165 abnormal endocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:15254591 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20190815 MGI PMID:14536066 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15249658 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15070754 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15249658 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009294 increased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17921248 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:14660788 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15249658 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009332 abnormal splenocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:17652179 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009535 abnormal skin sebaceous gland morphology IAGP N RGD:5509061 20141003 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15930296 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15231871 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15919792 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16845470 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010064 increased circulating creatine level IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19737866 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:10549290 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010678 abnormal skin adnexa morphology IAGP N RGD:5509061 20141003 MGI PMID:17652179 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010678 abnormal skin adnexa morphology IAGP N RGD:5509061 20141003 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:10549290 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010758 increased right ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:18382765 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010758 increased right ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:19801450 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:20519122 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:15067317 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:18059282 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0010964 increased compact bone volume IAGP N RGD:5509061 20141003 MGI PMID:21876000 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19117549 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11857800 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15231871 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15254591 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10549290 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15070754 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20190815 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20141003 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20160414 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011369 increased renal glomerulus apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:21135166 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011442 abnormal renal sodium ion transport IAGP N RGD:5509061 20141003 MGI PMID:15956187 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:19117549 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0012126 abnormal placenta hemotrichorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:10549290 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20191017 MGI PMID:31435015 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20220519 MGI 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20160407 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20190815 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:19117549 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0030923 abnormal hair follicle ostium morphology IAGP N RGD:5509061 20181220 MGI PMID:19052558 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:15249658 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:15919792 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:17003330 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:17465682 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:14536066 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:14603033 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:15716267 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:10549291 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0031607 abnormal fetal cardiomyocyte mitochondrial morphology IAGP N RGD:5509061 20240404 MGI PMID:10549290 69169 Pparg peroxisome proliferator activated receptor gamma gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:15716267 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:18668043 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:12147287 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:12147287 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:12147287 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11101840 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11101840 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21035764 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15147521 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0003327 liver cyst IAGP N RGD:5509061 20190418 MGI PMID:29154852 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20190418 MGI PMID:29154852 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:21035764 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0003675 kidney cyst IAGP N RGD:5509061 20190418 MGI PMID:29154852 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:18668043 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:17395745 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:11101840 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21035764 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21035764 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:18668043 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17395745 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21035764 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:15634780 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0005645 abnormal hypothalamus physiology IAGP N RGD:5509061 20141003 MGI PMID:18668043 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:15147521 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:18054322 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0006039 decreased mitochondrial fission IAGP N RGD:5509061 20141003 MGI PMID:15634780 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:15147521 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:15147521 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0008413 decreased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:15147521 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20190418 MGI PMID:29154852 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0009786 decreased susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11101840 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:15634780 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:15634780 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0013139 moribund IAGP N RGD:5509061 20190418 MGI PMID:29154852 69171 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier) gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:17395745 69200 a nonagouti gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18172198 69200 a nonagouti gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:14737183 69200 a nonagouti gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21779871 69200 a nonagouti gene MP:0000248 macrocytosis IAGP N RGD:5509061 20220616 MGI PMID:34354145 69200 a nonagouti gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:16578176 69200 a nonagouti gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:17247308 69200 a nonagouti gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:17247639 69200 a nonagouti gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:18057101 69200 a nonagouti gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:2379821 69200 a nonagouti gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:5726144 69200 a nonagouti gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:14737183 69200 a nonagouti gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:640377 69200 a nonagouti gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7751596 69200 a nonagouti gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7926745 69200 a nonagouti gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:14737183 69200 a nonagouti gene MP:0000421 mottled coat IAGP N RGD:5509061 20141003 MGI PMID:15890782 69200 a nonagouti gene MP:0000421 mottled coat IAGP N RGD:5509061 20141003 MGI PMID:5798139 69200 a nonagouti gene MP:0000421 mottled coat IAGP N RGD:5509061 20141003 MGI PMID:7926745 69200 a nonagouti gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:14737183 69200 a nonagouti gene MP:0000449 broad nasal bridge IAGP N RGD:5509061 20141003 MGI PMID:14737183 69200 a nonagouti gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0000566 synostosis IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20150528 MGI PMID:7976186 69200 a nonagouti gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20150528 MGI PMID:7976186 69200 a nonagouti gene MP:0000914 exencephaly IAGP N RGD:5509061 20150528 MGI PMID:7976186 69200 a nonagouti gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20150528 MGI PMID:7976186 69200 a nonagouti gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:18172198 69200 a nonagouti gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15472465 69200 a nonagouti gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18227763 69200 a nonagouti gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19168544 69200 a nonagouti gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:9657845 69200 a nonagouti gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12925742 69200 a nonagouti gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:17101998 69200 a nonagouti gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:18172198 69200 a nonagouti gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:21779871 69200 a nonagouti gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:5798139 69200 a nonagouti gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:7926745 69200 a nonagouti gene MP:0001261 obese IAGP N RGD:5509061 20141218 MGI PMID:18821597 69200 a nonagouti gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17873059 69200 a nonagouti gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18272480 69200 a nonagouti gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20050919 69200 a nonagouti gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14737183 69200 a nonagouti gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:14737183 69200 a nonagouti gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 69200 a nonagouti gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12548288 69200 a nonagouti gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16578176 69200 a nonagouti gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17247308 69200 a nonagouti gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17247639 69200 a nonagouti gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4634048 69200 a nonagouti gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18172198 69200 a nonagouti gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:18272480 69200 a nonagouti gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:20050919 69200 a nonagouti gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:18172198 69200 a nonagouti gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:1896452 69200 a nonagouti gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21779871 69200 a nonagouti gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21779871 69200 a nonagouti gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:18227763 69200 a nonagouti gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:21779871 69200 a nonagouti gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17101998 69200 a nonagouti gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:19168544 69200 a nonagouti gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 69200 a nonagouti gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:102659 69200 a nonagouti gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:13886198 69200 a nonagouti gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1473152 69200 a nonagouti gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17101998 69200 a nonagouti gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17247308 69200 a nonagouti gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17247639 69200 a nonagouti gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:2566558 69200 a nonagouti gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:2822532 69200 a nonagouti gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:3227730 69200 a nonagouti gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4065569 69200 a nonagouti gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:5726144 69200 a nonagouti gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:5798139 69200 a nonagouti gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:5968639 69200 a nonagouti gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7751596 69200 a nonagouti gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7926745 69200 a nonagouti gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21779871 69200 a nonagouti gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:1896452 69200 a nonagouti gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:2566558 69200 a nonagouti gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:4065569 69200 a nonagouti gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:14737183 69200 a nonagouti gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:21779871 69200 a nonagouti gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:6776948 69200 a nonagouti gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20220616 MGI PMID:34354145 69200 a nonagouti gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20220616 MGI PMID:34354145 69200 a nonagouti gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20220616 MGI PMID:34354145 69200 a nonagouti gene MP:0002642 anisocytosis IAGP N RGD:5509061 20220616 MGI PMID:34354145 69200 a nonagouti gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 69200 a nonagouti gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0002872 polycythemia IAGP N RGD:5509061 20220616 MGI PMID:34354145 69200 a nonagouti gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17247639 69200 a nonagouti gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:5726144 69200 a nonagouti gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:469221 69200 a nonagouti gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:17246842 69200 a nonagouti gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:18172198 69200 a nonagouti gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 69200 a nonagouti gene MP:0003121 genetic imprinting IAGP N RGD:5509061 20141003 MGI PMID:12601169 69200 a nonagouti gene MP:0003122 maternal imprinting IEA N RGD:5509061 20111116 MGI 69200 a nonagouti gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:15890782 69200 a nonagouti gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:17652101 69200 a nonagouti gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:18172198 69200 a nonagouti gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:5798139 69200 a nonagouti gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:7751596 69200 a nonagouti gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:7926745 69200 a nonagouti gene MP:0003171 phenotypic reversion IAGP N RGD:5509061 20141003 MGI PMID:2379821 69200 a nonagouti gene MP:0003171 phenotypic reversion IAGP N RGD:5509061 20141016 MGI PMID:24599260 69200 a nonagouti gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20050919 69200 a nonagouti gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20150528 MGI PMID:7976186 69200 a nonagouti gene MP:0003586 dilated ureter IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:640377 69200 a nonagouti gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:7926745 69200 a nonagouti gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:17247308 69200 a nonagouti gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20111116 MGI 69200 a nonagouti gene MP:0004165 abnormal lateral geniculate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:102659 69200 a nonagouti gene MP:0004356 radius hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17247639 69200 a nonagouti gene MP:0004382 abnormal hair follicle melanogenesis IAGP N RGD:5509061 20141003 MGI PMID:1409442 69200 a nonagouti gene MP:0004382 abnormal hair follicle melanogenesis IAGP N RGD:5509061 20181220 MGI PMID:23201126 69200 a nonagouti gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:12070017 69200 a nonagouti gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:2369371 69200 a nonagouti gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:6696991 69200 a nonagouti gene MP:0005071 enlarged hair follicle melanin granules IEA N RGD:5509061 20111116 MGI 69200 a nonagouti gene MP:0005072 abnormal hair follicle melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:17247308 69200 a nonagouti gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 69200 a nonagouti gene MP:0005077 abnormal melanogenesis IAGP N RGD:5509061 20141003 MGI PMID:4634048 69200 a nonagouti gene MP:0005100 abnormal choroid pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12548288 69200 a nonagouti gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16578176 69200 a nonagouti gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0005118 decreased circulating pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:9877102 69200 a nonagouti gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8125260 69200 a nonagouti gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141016 MGI PMID:24599260 69200 a nonagouti gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16578176 69200 a nonagouti gene MP:0005174 abnormal tail pigmentation IAGP N RGD:5509061 20160519 MGI PMID:10431243 69200 a nonagouti gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21779871 69200 a nonagouti gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:21779871 69200 a nonagouti gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141225 MGI PMID:14737183 69200 a nonagouti gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20050919 69200 a nonagouti gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21779871 69200 a nonagouti gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:21779871 69200 a nonagouti gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:2369371 69200 a nonagouti gene MP:0005353 abnormal patella morphology IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0005366 variegated coat color IAGP N RGD:5509061 20141003 MGI PMID:12601169 69200 a nonagouti gene MP:0005366 variegated coat color IAGP N RGD:5509061 20141003 MGI PMID:17101998 69200 a nonagouti gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:17247639 69200 a nonagouti gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:12533510 69200 a nonagouti gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:1896452 69200 a nonagouti gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:5962396 69200 a nonagouti gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:5968639 69200 a nonagouti gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:7751596 69200 a nonagouti gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141218 MGI PMID:18821597 69200 a nonagouti gene MP:0005409 darkened coat color IAGP N RGD:5509061 20150129 MGI PMID:20819186 69200 a nonagouti gene MP:0005409 darkened coat color IAGP N RGD:5509061 20181220 MGI PMID:23201126 69200 a nonagouti gene MP:0005430 absent fibula IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:10971147 69200 a nonagouti gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:15472465 69200 a nonagouti gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:18172198 69200 a nonagouti gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18172198 69200 a nonagouti gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:14737183 69200 a nonagouti gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20050919 69200 a nonagouti gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20240307 MGI PMID:10945631 69200 a nonagouti gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:12070017 69200 a nonagouti gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:6696991 69200 a nonagouti gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18172198 69200 a nonagouti gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21779871 69200 a nonagouti gene MP:0006370 abnormal hair follicle pheomelanosome pheomelanin content IAGP N RGD:5509061 20141003 MGI PMID:17652101 69200 a nonagouti gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:102659 69200 a nonagouti gene MP:0008237 abnormal ventral coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:14737183 69200 a nonagouti gene MP:0008237 abnormal ventral coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:3227730 69200 a nonagouti gene MP:0008237 abnormal ventral coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:5798139 69200 a nonagouti gene MP:0008238 abnormal dorsoventral coat patterning IAGP N RGD:5509061 20141003 MGI PMID:14737183 69200 a nonagouti gene MP:0008296 abnormal adrenal gland x-zone morphology IAGP N RGD:5509061 20141003 MGI PMID:7976166 69200 a nonagouti gene MP:0008480 absent eye pigmentation IAGP N RGD:5509061 20141016 MGI PMID:24599260 69200 a nonagouti gene MP:0008731 abnormal hair shaft melanin granule morphology IEA N RGD:5509061 20111116 MGI 69200 a nonagouti gene MP:0008732 reduced hair shaft melanin granule number IEA N RGD:5509061 20111116 MGI 69200 a nonagouti gene MP:0008733 abnormal hair shaft melanin granule distribution IAGP N RGD:5509061 20141003 MGI PMID:17247308 69200 a nonagouti gene MP:0008733 abnormal hair shaft melanin granule distribution IAGP N RGD:5509061 20141003 MGI PMID:17247639 69200 a nonagouti gene MP:0008762 embryonic lethality IEA N RGD:5509061 20111116 MGI 69200 a nonagouti gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0008919 fused tarsal bones IAGP N RGD:5509061 20141003 MGI PMID:2320577 69200 a nonagouti gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20150528 MGI PMID:7976186 69200 a nonagouti gene MP:0009255 degranulated pancreatic beta cells IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:20050919 69200 a nonagouti gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18172198 69200 a nonagouti gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18172198 69200 a nonagouti gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18172198 69200 a nonagouti gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20141003 MGI PMID:6696991 69200 a nonagouti gene MP:0009547 elliptocytosis IAGP N RGD:5509061 20220616 MGI PMID:34354145 69200 a nonagouti gene MP:0009554 abnormal hair follicle melanin granule shape IAGP N RGD:5509061 20141003 MGI PMID:17247308 69200 a nonagouti gene MP:0009555 abnormal hair follicle melanin granule distribution IAGP N RGD:5509061 20141003 MGI PMID:17247308 69200 a nonagouti gene MP:0009555 abnormal hair follicle melanin granule distribution IAGP N RGD:5509061 20141003 MGI PMID:4634048 69200 a nonagouti gene MP:0009557 decreased platelet ADP level IAGP N RGD:5509061 20141003 MGI PMID:6696991 69200 a nonagouti gene MP:0009568 abnormal red blood cell deformability IAGP N RGD:5509061 20220616 MGI PMID:34354145 69200 a nonagouti gene MP:0009928 abnormal pinna hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12644183 69200 a nonagouti gene MP:0009928 abnormal pinna hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:5962396 69200 a nonagouti gene MP:0009933 abnormal tail hair pigmentation IEA N RGD:5509061 20111229 MGI 69200 a nonagouti gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0010192 abnormal retina melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 69200 a nonagouti gene MP:0010193 abnormal choroid melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 69200 a nonagouti gene MP:0011093 embryonic lethality at implantation, complete penetrance IEA N RGD:5509061 20111116 MGI 69200 a nonagouti gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20111116 MGI 69200 a nonagouti gene MP:0011277 decreased tail pigmentation IEA N RGD:5509061 20111116 MGI 69200 a nonagouti gene MP:0011279 decreased ear pigmentation IAGP N RGD:5509061 20160519 MGI PMID:10431243 69200 a nonagouti gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20220616 MGI PMID:34354145 69200 a nonagouti gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:21779871 69200 a nonagouti gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:5468422 69200 a nonagouti gene MP:0011551 variegated eye pigmentation pattern IEA N RGD:5509061 20170209 MGI 69200 a nonagouti gene MP:0011627 decreased skin pigmentation IEA N RGD:5509061 20141003 MGI 69200 a nonagouti gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:18172198 69200 a nonagouti gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20141003 MGI PMID:12601169 69200 a nonagouti gene MP:0012167 abnormal epigenetic regulation of gene expression IAGP N RGD:5509061 20141003 MGI PMID:17101998 69200 a nonagouti gene MP:0013275 abnormal xenobiotic metabolism IAGP N RGD:5509061 20240307 MGI PMID:10945631 69200 a nonagouti gene MP:0014320 abnormal autopod rotation IAGP N RGD:5509061 20240404 MGI PMID:2320577 69200 a nonagouti gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170720 MGI PMID:6696991 69200 a nonagouti gene MP:0030050 large mandible IAGP N RGD:5509061 20170921 MGI PMID:19067046 69200 a nonagouti gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:21779871 69200 a nonagouti gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:18172198 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0000015 abnormal ear pigmentation IEA N RGD:5509061 20111116 MGI 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:12847290 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:6031677 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:15743322 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:102659 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:115747 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12777251 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:12777251 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:115747 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12777251 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15743322 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:12777251 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:3922995 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0002620 abnormal monocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12777251 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:115747 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:7089489 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0003174 increased lysosomal enzyme secretion IAGP N RGD:5509061 20141003 MGI PMID:6696991 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:2369371 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:6696991 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:12445206 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:6031677 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:9256466 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0005100 abnormal choroid pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9256466 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0005101 abnormal ciliary body pigmentation IAGP N RGD:5509061 20141003 MGI PMID:102659 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18715234 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:6031677 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:2369371 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:6696991 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:9256466 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:6696991 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:12777251 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12777251 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20141003 MGI PMID:6696991 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0009557 decreased platelet ADP level IAGP N RGD:5509061 20141003 MGI PMID:6696991 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:115747 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7089489 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0010815 enlarged alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:12777251 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0010815 enlarged alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:15743322 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0010922 alveolitis IAGP N RGD:5509061 20141003 MGI PMID:15743322 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0010950 abnormal lung hysteresivity IAGP N RGD:5509061 20141003 MGI PMID:12777251 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20141003 MGI 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0011090 perinatal lethality, incomplete penetrance IEA N RGD:5509061 20141003 MGI 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12847290 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:6031677 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0011279 decreased ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12847290 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0011279 decreased ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:6031677 69205 Hps1 HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170720 MGI PMID:9256466 69209 Msmb beta-microseminoprotein gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15674347 69209 Msmb beta-microseminoprotein gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:15674347 69209 Msmb beta-microseminoprotein gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:15674347 69209 Msmb beta-microseminoprotein gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15674347 69209 Msmb beta-microseminoprotein gene MP:0009739 enlarged prostate gland dorsolateral lobe IAGP N RGD:5509061 20220303 MGI PMID:15674347 69209 Msmb beta-microseminoprotein gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 69209 Msmb beta-microseminoprotein gene MP:0031357 enlarged prostate gland ventral lobe IAGP N RGD:5509061 20220303 MGI PMID:15674347 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20170406 MGI PMID:27912058 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20170406 MGI PMID:27912058 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170406 MGI PMID:27912058 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20170406 MGI PMID:27912058 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0001407 short stride length IAGP N RGD:5509061 20170406 MGI PMID:27912058 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20170406 MGI PMID:27912058 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0003860 abnormal carbon dioxide level IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20170406 MGI PMID:27912058 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20170406 MGI PMID:27912058 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20170406 MGI PMID:27912058 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16875466 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20170406 MGI PMID:27912058 69215 Bckdk branched chain ketoacid dehydrogenase kinase gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:27912058 69217 Clip1 CAP-GLY domain containing linker protein 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:16230537 69217 Clip1 CAP-GLY domain containing linker protein 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16230537 69217 Clip1 CAP-GLY domain containing linker protein 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:16230537 69217 Clip1 CAP-GLY domain containing linker protein 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:16230537 69217 Clip1 CAP-GLY domain containing linker protein 1 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:16230537 69217 Clip1 CAP-GLY domain containing linker protein 1 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20141003 MGI PMID:16230537 69217 Clip1 CAP-GLY domain containing linker protein 1 gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20141003 MGI PMID:16230537 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160804 MGI 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20160915 MGI PMID:26150517 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20210422 MGI PMID:31815201 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20160915 MGI PMID:26150517 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160915 MGI PMID:26150517 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20211021 MGI 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20141003 MGI 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20160804 MGI 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001577 anemia IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20180927 MGI PMID:29677191 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001627 abnormal cardiac output IAGP N RGD:5509061 20180927 MGI PMID:29677191 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20180927 MGI PMID:29677191 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001756 abnormal urination IEA N RGD:5509061 20160804 MGI 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20150122 MGI PMID:25163478 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20210422 MGI PMID:31815201 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:17010132 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20160915 MGI PMID:26150517 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20160915 MGI PMID:26150517 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0005018 decreased T cell number IEA N RGD:5509061 20160804 MGI 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20180927 MGI PMID:29677191 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0005152 pancytopenia IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0005316 abnormal response to tactile stimuli IEA N RGD:5509061 20141003 MGI 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0005407 hyperalgesia IAGP N RGD:5509061 20150122 MGI PMID:25163478 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20180927 MGI PMID:29677191 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0005443 abnormal ethanol metabolism IAGP N RGD:5509061 20150122 MGI PMID:25163478 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0005443 abnormal ethanol metabolism IAGP N RGD:5509061 20160915 MGI PMID:26150517 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20160804 MGI 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:10913633 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20160915 MGI PMID:26150517 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20180927 MGI PMID:29677191 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20160804 MGI 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20160804 MGI 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20210422 MGI PMID:31815201 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:17010132 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20160915 MGI PMID:26150517 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20160915 MGI PMID:26150517 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20160915 MGI PMID:26150517 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21734703 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20150122 MGI PMID:22922648 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:10913633 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20180927 MGI PMID:29677191 69218 Aldh2 aldehyde dehydrogenase 2, mitochondrial gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21734703 69438 G6pc2 glucose-6-phosphatase, catalytic, 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17265032 69438 G6pc2 glucose-6-phosphatase, catalytic, 2 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20439719 69438 G6pc2 glucose-6-phosphatase, catalytic, 2 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20439719 69438 G6pc2 glucose-6-phosphatase, catalytic, 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20439719 69438 G6pc2 glucose-6-phosphatase, catalytic, 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17265032 69438 G6pc2 glucose-6-phosphatase, catalytic, 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20439719 69440 Vgf VGF nerve growth factor inducible gene MP:0000231 hypertension IAGP N RGD:5509061 20151008 MGI PMID:24497580 69440 Vgf VGF nerve growth factor inducible gene MP:0000745 tremors IEA N RGD:5509061 20181227 MGI 69440 Vgf VGF nerve growth factor inducible gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18815270 69440 Vgf VGF nerve growth factor inducible gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 69440 Vgf VGF nerve growth factor inducible gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 69440 Vgf VGF nerve growth factor inducible gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:18815270 69440 Vgf VGF nerve growth factor inducible gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18815270 69440 Vgf VGF nerve growth factor inducible gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:18815270 69440 Vgf VGF nerve growth factor inducible gene MP:0001513 limb grasping IEA N RGD:5509061 20181227 MGI 69440 Vgf VGF nerve growth factor inducible gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 69440 Vgf VGF nerve growth factor inducible gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 69440 Vgf VGF nerve growth factor inducible gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20181227 MGI 69440 Vgf VGF nerve growth factor inducible gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:18815270 69440 Vgf VGF nerve growth factor inducible gene MP:0003962 abnormal adrenaline level IAGP N RGD:5509061 20151008 MGI PMID:24497580 69440 Vgf VGF nerve growth factor inducible gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20151008 MGI PMID:24497580 69440 Vgf VGF nerve growth factor inducible gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220519 MGI 69440 Vgf VGF nerve growth factor inducible gene MP:0005119 decreased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:18815270 69440 Vgf VGF nerve growth factor inducible gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 69440 Vgf VGF nerve growth factor inducible gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 69440 Vgf VGF nerve growth factor inducible gene MP:0005662 increased circulating adrenaline level IAGP N RGD:5509061 20151008 MGI PMID:24497580 69440 Vgf VGF nerve growth factor inducible gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20151008 MGI PMID:24497580 69440 Vgf VGF nerve growth factor inducible gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20151008 MGI PMID:24497580 69440 Vgf VGF nerve growth factor inducible gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0008289 abnormal adrenal medulla morphology IAGP N RGD:5509061 20151008 MGI PMID:24497580 69440 Vgf VGF nerve growth factor inducible gene MP:0008506 abnormal noradrenergic chromaffin cell morphology IAGP N RGD:5509061 20151008 MGI PMID:24497580 69440 Vgf VGF nerve growth factor inducible gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0009066 decreased oviduct weight IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 69440 Vgf VGF nerve growth factor inducible gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18815270 69440 Vgf VGF nerve growth factor inducible gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 69440 Vgf VGF nerve growth factor inducible gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 69440 Vgf VGF nerve growth factor inducible gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20151008 MGI PMID:24497580 69440 Vgf VGF nerve growth factor inducible gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:10433265 69440 Vgf VGF nerve growth factor inducible gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10433265 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20160804 MGI 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11409893 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0001123 dilated uterus IAGP N RGD:5509061 20141003 MGI PMID:11409893 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0001258 decreased body length IEA N RGD:5509061 20160804 MGI 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11409893 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11409893 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11409893 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0002681 increased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:11409893 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20141003 MGI 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20141003 MGI 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0004832 enlarged ovary IAGP N RGD:5509061 20141003 MGI PMID:11409893 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:11409893 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0009082 uterus cyst IAGP N RGD:5509061 20141003 MGI PMID:11409893 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20141003 MGI PMID:11409893 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:11409893 69444 Acsl4 acyl-CoA synthetase long-chain family member 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 69445 Acsl5 acyl-CoA synthetase long-chain family member 5 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20170323 MGI 69445 Acsl5 acyl-CoA synthetase long-chain family member 5 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20150430 MGI 69445 Acsl5 acyl-CoA synthetase long-chain family member 5 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 69445 Acsl5 acyl-CoA synthetase long-chain family member 5 gene MP:0001314 cornea opacity IEA N RGD:5509061 20150430 MGI 69445 Acsl5 acyl-CoA synthetase long-chain family member 5 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20150430 MGI 69445 Acsl5 acyl-CoA synthetase long-chain family member 5 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 69445 Acsl5 acyl-CoA synthetase long-chain family member 5 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20170323 MGI 69445 Acsl5 acyl-CoA synthetase long-chain family member 5 gene MP:0003402 decreased liver weight IEA N RGD:5509061 20210128 MGI 69445 Acsl5 acyl-CoA synthetase long-chain family member 5 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210128 MGI 69445 Acsl5 acyl-CoA synthetase long-chain family member 5 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20150430 MGI 69445 Acsl5 acyl-CoA synthetase long-chain family member 5 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20150430 MGI 69445 Acsl5 acyl-CoA synthetase long-chain family member 5 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210520 MGI 69445 Acsl5 acyl-CoA synthetase long-chain family member 5 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210520 MGI 69445 Acsl5 acyl-CoA synthetase long-chain family member 5 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20240523 MGI 69445 Acsl5 acyl-CoA synthetase long-chain family member 5 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20170323 MGI 69447 Acsl6 acyl-CoA synthetase long-chain family member 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190110 MGI PMID:30401738 69447 Acsl6 acyl-CoA synthetase long-chain family member 6 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20190110 MGI PMID:30401738 69447 Acsl6 acyl-CoA synthetase long-chain family member 6 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20190110 MGI PMID:30401738 69447 Acsl6 acyl-CoA synthetase long-chain family member 6 gene MP:0010762 abnormal microglial cell activation IAGP N RGD:5509061 20190110 MGI PMID:30401738 69447 Acsl6 acyl-CoA synthetase long-chain family member 6 gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20190110 MGI PMID:30401738 69447 Acsl6 acyl-CoA synthetase long-chain family member 6 gene MP:0013243 abnormal carbohydrate metabolism IAGP N RGD:5509061 20190110 MGI PMID:30401738 69447 Acsl6 acyl-CoA synthetase long-chain family member 6 gene MP:0020866 abnormal lipogenesis IAGP N RGD:5509061 20190110 MGI PMID:30401738 69447 Acsl6 acyl-CoA synthetase long-chain family member 6 gene MP:0020867 increased lipogenesis IAGP N RGD:5509061 20190110 MGI PMID:30401738 69447 Acsl6 acyl-CoA synthetase long-chain family member 6 gene MP:0020868 decreased lipogenesis IAGP N RGD:5509061 20190110 MGI PMID:30401738 69450 Pclo piccolo (presynaptic cytomatrix protein) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20332206 69450 Pclo piccolo (presynaptic cytomatrix protein) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20332206 69450 Pclo piccolo (presynaptic cytomatrix protein) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20332206 69450 Pclo piccolo (presynaptic cytomatrix protein) gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20170209 MGI PMID:26045179 69450 Pclo piccolo (presynaptic cytomatrix protein) gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:20332206 69450 Pclo piccolo (presynaptic cytomatrix protein) gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20170209 MGI PMID:26045179 69450 Pclo piccolo (presynaptic cytomatrix protein) gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:20332206 69450 Pclo piccolo (presynaptic cytomatrix protein) gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:20332206 69450 Pclo piccolo (presynaptic cytomatrix protein) gene MP:0008921 increased neurotransmitter release IAGP N RGD:5509061 20170209 MGI PMID:26045179 69450 Pclo piccolo (presynaptic cytomatrix protein) gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20170209 MGI PMID:26045179 69452 Sik1 salt inducible kinase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161110 MGI PMID:26844205 69452 Sik1 salt inducible kinase 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20161110 MGI PMID:26844205 69452 Sik1 salt inducible kinase 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20161110 MGI PMID:26844205 69452 Sik1 salt inducible kinase 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20161110 MGI PMID:26844205 69452 Sik1 salt inducible kinase 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20150430 MGI 69452 Sik1 salt inducible kinase 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20161110 MGI PMID:26844205 69452 Sik1 salt inducible kinase 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 69452 Sik1 salt inducible kinase 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20161110 MGI PMID:26844205 69452 Sik1 salt inducible kinase 1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20210128 MGI 69452 Sik1 salt inducible kinase 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150430 MGI 69452 Sik1 salt inducible kinase 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 69452 Sik1 salt inducible kinase 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20161110 MGI PMID:26844205 69452 Sik1 salt inducible kinase 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20231207 MGI 69452 Sik1 salt inducible kinase 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20161110 MGI PMID:26844205 69452 Sik1 salt inducible kinase 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20231207 MGI 69452 Sik1 salt inducible kinase 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20150430 MGI 69452 Sik1 salt inducible kinase 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 69452 Sik1 salt inducible kinase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20161110 MGI PMID:26844205 69452 Sik1 salt inducible kinase 1 gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:26844205 69454 Lcn2 lipocalin 2 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:16446425 69454 Lcn2 lipocalin 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15531878 69454 Lcn2 lipocalin 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16446425 69454 Lcn2 lipocalin 2 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 69454 Lcn2 lipocalin 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0002959 increased urine microalbumin level IEA N RGD:5509061 20201022 MGI 69454 Lcn2 lipocalin 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20230601 MGI 69454 Lcn2 lipocalin 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:15531878 69454 Lcn2 lipocalin 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 69454 Lcn2 lipocalin 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230601 MGI 69454 Lcn2 lipocalin 2 gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15531878 69454 Lcn2 lipocalin 2 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:21507940 69454 Lcn2 lipocalin 2 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20180111 MGI PMID:20332347 69454 Lcn2 lipocalin 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 69454 Lcn2 lipocalin 2 gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:20332347 69455 Asah2 N-acylsphingosine amidohydrolase 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:16380386 69457 Pacsin2 protein kinase C and casein kinase substrate in neurons 2 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20201022 MGI 69457 Pacsin2 protein kinase C and casein kinase substrate in neurons 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220519 MGI 69457 Pacsin2 protein kinase C and casein kinase substrate in neurons 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 69457 Pacsin2 protein kinase C and casein kinase substrate in neurons 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20201022 MGI 69457 Pacsin2 protein kinase C and casein kinase substrate in neurons 2 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20191003 MGI PMID:29107716 69457 Pacsin2 protein kinase C and casein kinase substrate in neurons 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20230601 MGI 69457 Pacsin2 protein kinase C and casein kinase substrate in neurons 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 69457 Pacsin2 protein kinase C and casein kinase substrate in neurons 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20191003 MGI PMID:29107716 69457 Pacsin2 protein kinase C and casein kinase substrate in neurons 2 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20201022 MGI 69457 Pacsin2 protein kinase C and casein kinase substrate in neurons 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20170105 MGI 69457 Pacsin2 protein kinase C and casein kinase substrate in neurons 2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20170105 MGI 69457 Pacsin2 protein kinase C and casein kinase substrate in neurons 2 gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20191003 MGI PMID:29107716 69457 Pacsin2 protein kinase C and casein kinase substrate in neurons 2 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20191003 MGI PMID:29107716 69457 Pacsin2 protein kinase C and casein kinase substrate in neurons 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20616007 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:20616007 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:20808283 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:20616007 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20160421 MGI 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:20616007 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20808283 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20808283 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:20616007 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0008160 increased diameter of humerus IAGP N RGD:5509061 20141003 MGI PMID:20616007 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:20616007 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20808283 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:20808283 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20808283 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:20808283 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:20616007 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:20616007 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0010929 increased osteoid thickness IAGP N RGD:5509061 20141003 MGI PMID:20616007 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20220922 MGI PMID:20616007 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:20616007 69459 Nbr1 NBR1, autophagy cargo receptor gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:20616007 69461 Rasgrf2 RAS protein-specific guanine nucleotide-releasing factor 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 69461 Rasgrf2 RAS protein-specific guanine nucleotide-releasing factor 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17923690 69461 Rasgrf2 RAS protein-specific guanine nucleotide-releasing factor 2 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:15029245 69461 Rasgrf2 RAS protein-specific guanine nucleotide-releasing factor 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17923690 69461 Rasgrf2 RAS protein-specific guanine nucleotide-releasing factor 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17923690 69461 Rasgrf2 RAS protein-specific guanine nucleotide-releasing factor 2 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17923690 69463 Glrx3 glutaredoxin 3 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:21575136 69463 Glrx3 glutaredoxin 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21575136 69463 Glrx3 glutaredoxin 3 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191128 MGI 69463 Glrx3 glutaredoxin 3 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191128 MGI 69463 Glrx3 glutaredoxin 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18929570 69463 Glrx3 glutaredoxin 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21575136 69463 Glrx3 glutaredoxin 3 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 69463 Glrx3 glutaredoxin 3 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18929570 69463 Glrx3 glutaredoxin 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 69463 Glrx3 glutaredoxin 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:21575136 69463 Glrx3 glutaredoxin 3 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191128 MGI 69463 Glrx3 glutaredoxin 3 gene MP:0003708 binucleate IAGP N RGD:5509061 20141003 MGI PMID:21575136 69463 Glrx3 glutaredoxin 3 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:18929570 69463 Glrx3 glutaredoxin 3 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:18929570 69463 Glrx3 glutaredoxin 3 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:18929570 69463 Glrx3 glutaredoxin 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18929570 69463 Glrx3 glutaredoxin 3 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:21575136 69463 Glrx3 glutaredoxin 3 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191128 MGI 69463 Glrx3 glutaredoxin 3 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 69463 Glrx3 glutaredoxin 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21575136 69463 Glrx3 glutaredoxin 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18929570 69463 Glrx3 glutaredoxin 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 69463 Glrx3 glutaredoxin 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18929570 69463 Glrx3 glutaredoxin 3 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:21575136 69463 Glrx3 glutaredoxin 3 gene MP:0012724 absent head fold IEA N RGD:5509061 20191128 MGI 69463 Glrx3 glutaredoxin 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20191128 MGI 69463 Glrx3 glutaredoxin 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20150827 MGI PMID:25158856 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20240222 MGI PMID:33932340 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180222 MGI PMID:28106097 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20150827 MGI PMID:25158856 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20150827 MGI PMID:25158856 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20150827 MGI PMID:25158856 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20150827 MGI PMID:25158856 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20150827 MGI PMID:25158856 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220714 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0014467 increased sperm mitochondrial size IAGP N RGD:5509061 20240613 MGI PMID:35469022 69465 Lancl1 LanC (bacterial lantibiotic synthetase component C)-like 1 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220714 MGI PMID:35469022 69469 Ubd ubiquitin D gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20200514 MGI 69469 Ubd ubiquitin D gene MP:0000706 small thymus IEA N RGD:5509061 20200514 MGI 69469 Ubd ubiquitin D gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20200514 MGI 69469 Ubd ubiquitin D gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16782901 69469 Ubd ubiquitin D gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16782901 69469 Ubd ubiquitin D gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16782901 69469 Ubd ubiquitin D gene MP:0009454 impaired contextual conditioning behavior IEA N RGD:5509061 20220811 MGI 69469 Ubd ubiquitin D gene MP:0013522 decreased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20211021 MGI 69469 Ubd ubiquitin D gene MP:0013883 increased CD4-positive, CD25-positive NK T cell number IEA N RGD:5509061 20211021 MGI 69474 Srebf1 sterol regulatory element binding transcription factor 1 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16046411 69474 Srebf1 sterol regulatory element binding transcription factor 1 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:19564420 69474 Srebf1 sterol regulatory element binding transcription factor 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11782483 69474 Srebf1 sterol regulatory element binding transcription factor 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16046411 69474 Srebf1 sterol regulatory element binding transcription factor 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9329978 69474 Srebf1 sterol regulatory element binding transcription factor 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11782483 69474 Srebf1 sterol regulatory element binding transcription factor 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16046411 69474 Srebf1 sterol regulatory element binding transcription factor 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9329978 69474 Srebf1 sterol regulatory element binding transcription factor 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:9329978 69474 Srebf1 sterol regulatory element binding transcription factor 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19564420 69474 Srebf1 sterol regulatory element binding transcription factor 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11782483 69474 Srebf1 sterol regulatory element binding transcription factor 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9329978 69474 Srebf1 sterol regulatory element binding transcription factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9329978 69474 Srebf1 sterol regulatory element binding transcription factor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9329978 69474 Srebf1 sterol regulatory element binding transcription factor 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9329978 69476 Ube2d2a ubiquitin-conjugating enzyme E2D 2A gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:16024774 69479 Oprk1 opioid receptor, kappa 1 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:9463367 69479 Oprk1 opioid receptor, kappa 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20170713 MGI PMID:23446450 69479 Oprk1 opioid receptor, kappa 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:9463367 69479 Oprk1 opioid receptor, kappa 1 gene MP:0001462 abnormal avoidance learning behavior IAGP N RGD:5509061 20141003 MGI PMID:19864633 69479 Oprk1 opioid receptor, kappa 1 gene MP:0001934 increased litter size IAGP N RGD:5509061 20141003 MGI PMID:9463367 69479 Oprk1 opioid receptor, kappa 1 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:9463367 69479 Oprk1 opioid receptor, kappa 1 gene MP:0001980 abnormal chemically-elicited antinociception IAGP N RGD:5509061 20170309 MGI PMID:26377476 69479 Oprk1 opioid receptor, kappa 1 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:16672569 69479 Oprk1 opioid receptor, kappa 1 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20170713 MGI PMID:23446450 69479 Oprk1 opioid receptor, kappa 1 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20170309 MGI PMID:26377476 69479 Oprk1 opioid receptor, kappa 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20170309 MGI PMID:26377476 69479 Oprk1 opioid receptor, kappa 1 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20170713 MGI PMID:23446450 69479 Oprk1 opioid receptor, kappa 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20141003 MGI PMID:9463367 69479 Oprk1 opioid receptor, kappa 1 gene MP:0009778 impaired behavioral response to anesthetic IAGP N RGD:5509061 20141003 MGI PMID:11032994 69479 Oprk1 opioid receptor, kappa 1 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20170309 MGI PMID:26377476 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220519 MGI 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0001148 enlarged testis IEA N RGD:5509061 20210826 MGI 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210128 MGI 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210128 MGI 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20210610 MGI PMID:33773101 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21411764 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210610 MGI PMID:33773101 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0005390 skeleton phenotype IAGP N RGD:5509061 20210610 MGI PMID:33773101 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20210610 MGI PMID:33773101 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20210610 MGI PMID:33773101 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0010768 mortality/aging IAGP N RGD:5509061 20210610 MGI PMID:33773101 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20210610 MGI PMID:33773101 69482 Pdk2 pyruvate dehydrogenase kinase, isoenzyme 2 gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20210610 MGI PMID:33773101 69484 Sycp2 synaptonemal complex protein 2 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:16717126 69484 Sycp2 synaptonemal complex protein 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:16717126 69484 Sycp2 synaptonemal complex protein 2 gene MP:0001147 small testis IEA N RGD:5509061 20210520 MGI 69484 Sycp2 synaptonemal complex protein 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:16717126 69484 Sycp2 synaptonemal complex protein 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:16717126 69484 Sycp2 synaptonemal complex protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16717126 69484 Sycp2 synaptonemal complex protein 2 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:16717126 69484 Sycp2 synaptonemal complex protein 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:16717126 69484 Sycp2 synaptonemal complex protein 2 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:16717126 69484 Sycp2 synaptonemal complex protein 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16717126 69484 Sycp2 synaptonemal complex protein 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:16717126 69484 Sycp2 synaptonemal complex protein 2 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:16717126 69484 Sycp2 synaptonemal complex protein 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:16717126 69484 Sycp2 synaptonemal complex protein 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:16717126 69486 Stx1a syntaxin 1A (brain) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18713622 69486 Stx1a syntaxin 1A (brain) gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:20576034 69486 Stx1a syntaxin 1A (brain) gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:24136198 69486 Stx1a syntaxin 1A (brain) gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16723534 69486 Stx1a syntaxin 1A (brain) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16723534 69486 Stx1a syntaxin 1A (brain) gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:20576034 69486 Stx1a syntaxin 1A (brain) gene MP:0001752 abnormal hypothalamus secretion IAGP N RGD:5509061 20141003 MGI PMID:20576034 69486 Stx1a syntaxin 1A (brain) gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:24136198 69486 Stx1a syntaxin 1A (brain) gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 69486 Stx1a syntaxin 1A (brain) gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18703708 69486 Stx1a syntaxin 1A (brain) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:16723534 69486 Stx1a syntaxin 1A (brain) gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:24136198 69486 Stx1a syntaxin 1A (brain) gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:24136198 69486 Stx1a syntaxin 1A (brain) gene MP:0002923 increased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:24136198 69486 Stx1a syntaxin 1A (brain) gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141218 MGI PMID:24587181 69486 Stx1a syntaxin 1A (brain) gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:24136198 69486 Stx1a syntaxin 1A (brain) gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:20576034 69486 Stx1a syntaxin 1A (brain) gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:20576034 69486 Stx1a syntaxin 1A (brain) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18713622 69486 Stx1a syntaxin 1A (brain) gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:18713622 69486 Stx1a syntaxin 1A (brain) gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141218 MGI PMID:24587181 69486 Stx1a syntaxin 1A (brain) gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:18703708 69486 Stx1a syntaxin 1A (brain) gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:24136198 69486 Stx1a syntaxin 1A (brain) gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:24136198 69486 Stx1a syntaxin 1A (brain) gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:24136198 69486 Stx1a syntaxin 1A (brain) gene MP:0006299 abnormal latent inhibition of conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:20576034 69486 Stx1a syntaxin 1A (brain) gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:24136198 69486 Stx1a syntaxin 1A (brain) gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20141218 MGI PMID:24587181 69486 Stx1a syntaxin 1A (brain) gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:24136198 69486 Stx1a syntaxin 1A (brain) gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141218 MGI PMID:24587181 69486 Stx1a syntaxin 1A (brain) gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 69486 Stx1a syntaxin 1A (brain) gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:20576034 69486 Stx1a syntaxin 1A (brain) gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18713622 69486 Stx1a syntaxin 1A (brain) gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141218 MGI PMID:24587181 69486 Stx1a syntaxin 1A (brain) gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18713622 69486 Stx1a syntaxin 1A (brain) gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141218 MGI PMID:24587181 69486 Stx1a syntaxin 1A (brain) gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20240523 MGI 69486 Stx1a syntaxin 1A (brain) gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:24587181 69486 Stx1a syntaxin 1A (brain) gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:24587181 69486 Stx1a syntaxin 1A (brain) gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:24136198 69488 Ccn4 cellular communication network factor 4 gene MP:0001405 impaired coordination IEA N RGD:5509061 20141003 MGI 69490 Ugt2a1 UDP glucuronosyltransferase 2 family, polypeptide A1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220811 MGI 69492 Synj1 synaptojanin 1 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20181227 MGI 69492 Synj1 synaptojanin 1 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20181227 MGI 69492 Synj1 synaptojanin 1 gene MP:0000745 tremors IEA N RGD:5509061 20160421 MGI 69492 Synj1 synaptojanin 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:10535736 69492 Synj1 synaptojanin 1 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:10535736 69492 Synj1 synaptojanin 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10535736 69492 Synj1 synaptojanin 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10535736 69492 Synj1 synaptojanin 1 gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:10535736 69492 Synj1 synaptojanin 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 69492 Synj1 synaptojanin 1 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 69492 Synj1 synaptojanin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10535736 69492 Synj1 synaptojanin 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10535736 69492 Synj1 synaptojanin 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12904583 69492 Synj1 synaptojanin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 69493 Tcam1 testicular cell adhesion molecule 1 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20151112 MGI PMID:19766163 69495 Synj2 synaptojanin 2 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:21423608 69495 Synj2 synaptojanin 2 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 69495 Synj2 synaptojanin 2 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:21423608 69495 Synj2 synaptojanin 2 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21423608 69495 Synj2 synaptojanin 2 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21423608 69495 Synj2 synaptojanin 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21423608 69495 Synj2 synaptojanin 2 gene MP:0004528 fused outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:21423608 69495 Synj2 synaptojanin 2 gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:21423608 69495 Synj2 synaptojanin 2 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:21423608 69495 Synj2 synaptojanin 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:21423608 69495 Synj2 synaptojanin 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21423608 69497 Pick1 protein interacting with C kinase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19258705 69497 Pick1 protein interacting with C kinase 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:19258705 69497 Pick1 protein interacting with C kinase 1 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:16543133 69497 Pick1 protein interacting with C kinase 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:15797551 69497 Pick1 protein interacting with C kinase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19258705 69497 Pick1 protein interacting with C kinase 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19258705 69497 Pick1 protein interacting with C kinase 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19258705 69497 Pick1 protein interacting with C kinase 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19258705 69497 Pick1 protein interacting with C kinase 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19258705 69497 Pick1 protein interacting with C kinase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19258705 69497 Pick1 protein interacting with C kinase 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19258705 69497 Pick1 protein interacting with C kinase 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:19258705 69497 Pick1 protein interacting with C kinase 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20161117 MGI PMID:26306493 69497 Pick1 protein interacting with C kinase 1 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19258705 69497 Pick1 protein interacting with C kinase 1 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20161117 MGI PMID:26306493 69497 Pick1 protein interacting with C kinase 1 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220224 MGI PMID:19258705 69497 Pick1 protein interacting with C kinase 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:19258705 69498 Rcan2 regulator of calcineurin 2 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:16648267 69498 Rcan2 regulator of calcineurin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21298050 69498 Rcan2 regulator of calcineurin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21298050 69498 Rcan2 regulator of calcineurin 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16648267 69498 Rcan2 regulator of calcineurin 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21298050 69498 Rcan2 regulator of calcineurin 2 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:16648267 69498 Rcan2 regulator of calcineurin 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21298050 69498 Rcan2 regulator of calcineurin 2 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16648267 69498 Rcan2 regulator of calcineurin 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:21298050 69498 Rcan2 regulator of calcineurin 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:16648267 69498 Rcan2 regulator of calcineurin 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21298050 69498 Rcan2 regulator of calcineurin 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16648267 69498 Rcan2 regulator of calcineurin 2 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:21298050 69498 Rcan2 regulator of calcineurin 2 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:16648267 69498 Rcan2 regulator of calcineurin 2 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16648267 69498 Rcan2 regulator of calcineurin 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16648267 69498 Rcan2 regulator of calcineurin 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21298050 69498 Rcan2 regulator of calcineurin 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16648267 69498 Rcan2 regulator of calcineurin 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16648267 69498 Rcan2 regulator of calcineurin 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:21298050 69498 Rcan2 regulator of calcineurin 2 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21298050 69498 Rcan2 regulator of calcineurin 2 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:21298050 69498 Rcan2 regulator of calcineurin 2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:21298050 69498 Rcan2 regulator of calcineurin 2 gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:21298050 69498 Rcan2 regulator of calcineurin 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:21298050 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151112 MGI PMID:21926968 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20151112 MGI PMID:21926968 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20151112 MGI PMID:21926968 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20151112 MGI PMID:21926968 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230119 MGI 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20151112 MGI PMID:21926968 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20151112 MGI PMID:21926968 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20151112 MGI PMID:21926968 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20151112 MGI PMID:21926968 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20151112 MGI PMID:21926968 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20151112 MGI PMID:21926968 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20151112 MGI PMID:21926968 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20151112 MGI PMID:21926968 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:22488361 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:22488361 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22488361 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20151112 MGI PMID:21926968 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20151112 MGI PMID:21926968 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:21926968 69655 Pacsin1 protein kinase C and casein kinase substrate in neurons 1 gene MP:0020082 increased hippocampus volume IAGP N RGD:5509061 20151112 MGI PMID:21926968 69658 Slc13a3 solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 3 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20220519 MGI 69658 Slc13a3 solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 3 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20221215 MGI 69658 Slc13a3 solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20240704 MGI PMID:38282243 69658 Slc13a3 solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 3 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20240704 MGI PMID:38282243 69658 Slc13a3 solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 3 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20220519 MGI 69658 Slc13a3 solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 3 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20181227 MGI 69658 Slc13a3 solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 3 gene MP:0005575 increased pulmonary ventilation IEA N RGD:5509061 20211021 MGI 69658 Slc13a3 solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 3 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20240704 MGI PMID:38282243 69661 Snrk SNF related kinase gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0000274 enlarged heart IAGP N RGD:5509061 20160929 MGI PMID:25505152 69661 Snrk SNF related kinase gene MP:0001260 increased body weight IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20160929 MGI PMID:25505152 69661 Snrk SNF related kinase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0002083 premature death IAGP N RGD:5509061 20160929 MGI PMID:25505152 69661 Snrk SNF related kinase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20160929 MGI PMID:25505152 69661 Snrk SNF related kinase gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20160929 MGI PMID:25505152 69661 Snrk SNF related kinase gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20160929 MGI PMID:25505152 69661 Snrk SNF related kinase gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20160929 MGI PMID:25505152 69661 Snrk SNF related kinase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0005331 insulin resistance IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20160929 MGI PMID:25505152 69661 Snrk SNF related kinase gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20190411 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160929 MGI PMID:25505152 69661 Snrk SNF related kinase gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240321 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0031603 brown adipose tissue inflammation IAGP N RGD:5509061 20240321 MGI PMID:29298809 69661 Snrk SNF related kinase gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:25505152 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17409116 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17409116 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17409116 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:17409231 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:9169529 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0001909 reduced NMDA receptor mediated synaptic activity in barrel cortex IAGP N RGD:5509061 20141003 MGI PMID:15509762 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20191017 MGI PMID:11248026 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0002059 abnormal seminal vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11248026 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:15509762 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:15509762 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17409116 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17409231 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:9169529 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15509762 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:9169529 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20150924 MGI PMID:11248026 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:17409231 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0010211 abnormal acute phase protein level IAGP N RGD:5509061 20141003 MGI PMID:17409116 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0011904 abnormal Schwann cell physiology IAGP N RGD:5509061 20220120 MGI PMID:17409231 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0011907 decreased Schwann cell proliferation IAGP N RGD:5509061 20220120 MGI PMID:17409231 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0013320 dilated seminal vesicle IAGP N RGD:5509061 20141204 MGI PMID:11248026 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0013899 abnormal seminal vesicle epithelium morphology IAGP N RGD:5509061 20150924 MGI PMID:11248026 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0013903 abnormal seminal vesicle fluid composition IAGP N RGD:5509061 20150924 MGI PMID:11248026 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0031330 delayed peripheral nervous system regeneration IAGP N RGD:5509061 20220120 MGI PMID:17409231 70077 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 gene MP:0031435 abnormal copulatory plug biosynthesis IAGP N RGD:5509061 20220922 MGI PMID:11248026 70079 Myo1a myosin IA gene MP:0001513 limb grasping IEA N RGD:5509061 20230601 MGI 70079 Myo1a myosin IA gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20141003 MGI PMID:15758024 70079 Myo1a myosin IA gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20240523 MGI 70079 Myo1a myosin IA gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20240523 MGI 70081 Akap10 A kinase anchor protein 10 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 70081 Akap10 A kinase anchor protein 10 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 70081 Akap10 A kinase anchor protein 10 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:17485678 70081 Akap10 A kinase anchor protein 10 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17485678 70081 Akap10 A kinase anchor protein 10 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20211021 MGI 70081 Akap10 A kinase anchor protein 10 gene MP:0003928 increased heart rate variability IAGP N RGD:5509061 20141003 MGI PMID:17485678 70081 Akap10 A kinase anchor protein 10 gene MP:0004070 abnormal P wave IAGP N RGD:5509061 20141003 MGI PMID:17485678 70081 Akap10 A kinase anchor protein 10 gene MP:0004122 abnormal sinus arrhythmia IAGP N RGD:5509061 20141003 MGI PMID:17485678 70081 Akap10 A kinase anchor protein 10 gene MP:0004184 abnormal baroreceptor physiology IAGP N RGD:5509061 20141003 MGI PMID:17485678 70081 Akap10 A kinase anchor protein 10 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17485678 70081 Akap10 A kinase anchor protein 10 gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:17485678 70081 Akap10 A kinase anchor protein 10 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:17485678 70081 Akap10 A kinase anchor protein 10 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:23968836 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23968836 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23968836 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:23968836 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15870291 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21215802 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15870291 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:21215802 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20111116 MGI 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23968836 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:15870291 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19638972 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:21215802 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141225 MGI PMID:25469849 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:23968836 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:21215802 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21215802 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20210826 MGI 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210826 MGI 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20111116 MGI 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0005526 decreased renal plasma flow rate IAGP N RGD:5509061 20141003 MGI PMID:19958325 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141225 MGI PMID:25469849 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23968836 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20170706 MGI PMID:23968836 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:23968836 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:21215802 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20141003 MGI PMID:15870291 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141225 MGI PMID:25469849 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19958325 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0009776 decreased behavioral withdrawal response IAGP N RGD:5509061 20141003 MGI PMID:15870291 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20111116 MGI 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141225 MGI PMID:25469849 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23968836 70083 Rgs4 regulator of G-protein signaling 4 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15870291 70501 Cdk2 cyclin dependent kinase 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:17700700 70501 Cdk2 cyclin dependent kinase 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19383288 70501 Cdk2 cyclin dependent kinase 2 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17700700 70501 Cdk2 cyclin dependent kinase 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17700700 70501 Cdk2 cyclin dependent kinase 2 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19383288 70501 Cdk2 cyclin dependent kinase 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:19383288 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12923533 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12923533 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:12923533 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12923533 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15315761 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19383288 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22331465 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19383288 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001627 abnormal cardiac output IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:19383288 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17700700 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:22331465 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:12923533 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:15315761 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20220623 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20220623 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:12923533 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:15315761 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:12923533 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:15315761 70501 Cdk2 cyclin dependent kinase 2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12923533 70501 Cdk2 cyclin dependent kinase 2 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20609353 70501 Cdk2 cyclin dependent kinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20609353 70501 Cdk2 cyclin dependent kinase 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19383288 70501 Cdk2 cyclin dependent kinase 2 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:12923533 70501 Cdk2 cyclin dependent kinase 2 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12923533 70501 Cdk2 cyclin dependent kinase 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:12923533 70501 Cdk2 cyclin dependent kinase 2 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19383288 70501 Cdk2 cyclin dependent kinase 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:19383288 70501 Cdk2 cyclin dependent kinase 2 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:12923533 70501 Cdk2 cyclin dependent kinase 2 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:22331465 70501 Cdk2 cyclin dependent kinase 2 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19383288 70501 Cdk2 cyclin dependent kinase 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:19383288 70501 Cdk2 cyclin dependent kinase 2 gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:17700700 70501 Cdk2 cyclin dependent kinase 2 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:19383288 70501 Cdk2 cyclin dependent kinase 2 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:12923533 70501 Cdk2 cyclin dependent kinase 2 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0004894 uterus atrophy IAGP N RGD:5509061 20141003 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:22331465 70501 Cdk2 cyclin dependent kinase 2 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:19383288 70501 Cdk2 cyclin dependent kinase 2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17700700 70501 Cdk2 cyclin dependent kinase 2 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19383288 70501 Cdk2 cyclin dependent kinase 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17700700 70501 Cdk2 cyclin dependent kinase 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22331465 70501 Cdk2 cyclin dependent kinase 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17700700 70501 Cdk2 cyclin dependent kinase 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16678773 70501 Cdk2 cyclin dependent kinase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0011122 absent primordial ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:14561402 70501 Cdk2 cyclin dependent kinase 2 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:19383288 70501 Cdk2 cyclin dependent kinase 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:18787066 70501 Cdk2 cyclin dependent kinase 2 gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:16678773 70503 Tfrc transferrin receptor gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0000088 short mandible IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20221117 MGI PMID:28466468 70503 Tfrc transferrin receptor gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0001263 weight loss IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0001406 abnormal gait IEA N RGD:5509061 20200514 MGI 70503 Tfrc transferrin receptor gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20200514 MGI 70503 Tfrc transferrin receptor gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0001670 abnormal intestinal mineral absorption IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0001954 respiratory distress IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0002083 premature death IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20221117 MGI PMID:28466468 70503 Tfrc transferrin receptor gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:21553221 70503 Tfrc transferrin receptor gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20221117 MGI PMID:28466468 70503 Tfrc transferrin receptor gene MP:0002639 micrognathia IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20221117 MGI PMID:28466468 70503 Tfrc transferrin receptor gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20221117 MGI PMID:28466468 70503 Tfrc transferrin receptor gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21553221 70503 Tfrc transferrin receptor gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20221117 MGI PMID:28466468 70503 Tfrc transferrin receptor gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0003292 melena IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:18316026 70503 Tfrc transferrin receptor gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0005036 diarrhea IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:21553221 70503 Tfrc transferrin receptor gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20221117 MGI PMID:28466468 70503 Tfrc transferrin receptor gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0008380 abnormal gonial bone morphology IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:18316026 70503 Tfrc transferrin receptor gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:10791995 70503 Tfrc transferrin receptor gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0009511 distended stomach IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20221117 MGI PMID:28466468 70503 Tfrc transferrin receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20151022 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 70503 Tfrc transferrin receptor gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:10192390 70503 Tfrc transferrin receptor gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 70503 Tfrc transferrin receptor gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0014083 blunted small intestinal villi IAGP N RGD:5509061 20160414 MGI PMID:26324903 70503 Tfrc transferrin receptor gene MP:0021164 oral cleft IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0030026 small Meckel's cartilage IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0030258 small mandibular condyloid process IAGP N RGD:5509061 20221006 MGI PMID:27362800 70503 Tfrc transferrin receptor gene MP:0030283 small mandibular coronoid process IAGP N RGD:5509061 20221006 MGI PMID:27362800 70505 Tert telomerase reverse transcriptase gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22341455 70505 Tert telomerase reverse transcriptase gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22341455 70505 Tert telomerase reverse transcriptase gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22341455 70505 Tert telomerase reverse transcriptase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16651430 70505 Tert telomerase reverse transcriptase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:16651430 70505 Tert telomerase reverse transcriptase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22341455 70505 Tert telomerase reverse transcriptase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10583505 70505 Tert telomerase reverse transcriptase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19571879 70505 Tert telomerase reverse transcriptase gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0003155 abnormal telomere length IAGP N RGD:5509061 20141003 MGI PMID:11102810 70505 Tert telomerase reverse transcriptase gene MP:0003155 abnormal telomere length IAGP N RGD:5509061 20141003 MGI PMID:15282303 70505 Tert telomerase reverse transcriptase gene MP:0003155 abnormal telomere length IAGP N RGD:5509061 20141003 MGI PMID:17965232 70505 Tert telomerase reverse transcriptase gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:16651430 70505 Tert telomerase reverse transcriptase gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:22341455 70505 Tert telomerase reverse transcriptase gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:19571879 70505 Tert telomerase reverse transcriptase gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22341455 70505 Tert telomerase reverse transcriptase gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:16651430 70505 Tert telomerase reverse transcriptase gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:22341455 70505 Tert telomerase reverse transcriptase gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:11102810 70505 Tert telomerase reverse transcriptase gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16651430 70505 Tert telomerase reverse transcriptase gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16651430 70505 Tert telomerase reverse transcriptase gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:19571879 70505 Tert telomerase reverse transcriptase gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:19571879 70505 Tert telomerase reverse transcriptase gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22341455 70505 Tert telomerase reverse transcriptase gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20022886 70505 Tert telomerase reverse transcriptase gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16651430 70505 Tert telomerase reverse transcriptase gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17965232 70505 Tert telomerase reverse transcriptase gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22341455 70505 Tert telomerase reverse transcriptase gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20170413 MGI PMID:26555817 70505 Tert telomerase reverse transcriptase gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20170413 MGI PMID:26555817 70505 Tert telomerase reverse transcriptase gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22341455 70505 Tert telomerase reverse transcriptase gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:11102810 70505 Tert telomerase reverse transcriptase gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22341455 70505 Tert telomerase reverse transcriptase gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22341455 70505 Tert telomerase reverse transcriptase gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0010266 decreased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16651430 70505 Tert telomerase reverse transcriptase gene MP:0011807 decreased lung fibroblast proliferation IAGP N RGD:5509061 20170413 MGI PMID:26555817 70505 Tert telomerase reverse transcriptase gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:22341455 70505 Tert telomerase reverse transcriptase gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:16651430 70505 Tert telomerase reverse transcriptase gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:21113150 70505 Tert telomerase reverse transcriptase gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:22341455 70505 Tert telomerase reverse transcriptase gene MP:0030928 increased telomere length IAGP N RGD:5509061 20190117 MGI PMID:22341455 70823 Fgf2 fibroblast growth factor 2 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:17872976 70823 Fgf2 fibroblast growth factor 2 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:12917328 70823 Fgf2 fibroblast growth factor 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12917328 70823 Fgf2 fibroblast growth factor 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9687490 70823 Fgf2 fibroblast growth factor 2 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:9576942 70823 Fgf2 fibroblast growth factor 2 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:9576942 70823 Fgf2 fibroblast growth factor 2 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:9687490 70823 Fgf2 fibroblast growth factor 2 gene MP:0000798 abnormal frontal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:9576942 70823 Fgf2 fibroblast growth factor 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 70823 Fgf2 fibroblast growth factor 2 gene MP:0001513 limb grasping IEA N RGD:5509061 20160421 MGI 70823 Fgf2 fibroblast growth factor 2 gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:9687490 70823 Fgf2 fibroblast growth factor 2 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:12917328 70823 Fgf2 fibroblast growth factor 2 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:19056741 70823 Fgf2 fibroblast growth factor 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:10688672 70823 Fgf2 fibroblast growth factor 2 gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:10688672 70823 Fgf2 fibroblast growth factor 2 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15621532 70823 Fgf2 fibroblast growth factor 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11826116 70823 Fgf2 fibroblast growth factor 2 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:10688672 70823 Fgf2 fibroblast growth factor 2 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:9576942 70823 Fgf2 fibroblast growth factor 2 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 70823 Fgf2 fibroblast growth factor 2 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:9461194 70823 Fgf2 fibroblast growth factor 2 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:17872976 70823 Fgf2 fibroblast growth factor 2 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12917328 70823 Fgf2 fibroblast growth factor 2 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17150229 70823 Fgf2 fibroblast growth factor 2 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:9687490 70823 Fgf2 fibroblast growth factor 2 gene MP:0003248 loss of glutamate neurons IAGP N RGD:5509061 20141003 MGI PMID:11826116 70823 Fgf2 fibroblast growth factor 2 gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:17071606 70823 Fgf2 fibroblast growth factor 2 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:17150229 70823 Fgf2 fibroblast growth factor 2 gene MP:0003824 decreased left ventricle developed pressure IAGP N RGD:5509061 20141003 MGI PMID:9461194 70823 Fgf2 fibroblast growth factor 2 gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:12917328 70823 Fgf2 fibroblast growth factor 2 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:17150229 70823 Fgf2 fibroblast growth factor 2 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:12917328 70823 Fgf2 fibroblast growth factor 2 gene MP:0004184 abnormal baroreceptor physiology IAGP N RGD:5509061 20141003 MGI PMID:9687490 70823 Fgf2 fibroblast growth factor 2 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9461194 70823 Fgf2 fibroblast growth factor 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17150229 70823 Fgf2 fibroblast growth factor 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:9461194 70823 Fgf2 fibroblast growth factor 2 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 70823 Fgf2 fibroblast growth factor 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:9687490 70823 Fgf2 fibroblast growth factor 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:9687490 70823 Fgf2 fibroblast growth factor 2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9461194 70823 Fgf2 fibroblast growth factor 2 gene MP:0008221 abnormal hippocampal commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:9687490 70823 Fgf2 fibroblast growth factor 2 gene MP:0008503 abnormal spinal cord grey matter morphology IAGP N RGD:5509061 20141003 MGI PMID:9687490 70823 Fgf2 fibroblast growth factor 2 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10688672 70823 Fgf2 fibroblast growth factor 2 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:15621532 70823 Fgf2 fibroblast growth factor 2 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:12917328 70823 Fgf2 fibroblast growth factor 2 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:12917328 70823 Fgf2 fibroblast growth factor 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:11320217 70823 Fgf2 fibroblast growth factor 2 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11826116 70823 Fgf2 fibroblast growth factor 2 gene MP:0009974 decreased cerebral cortex pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:11826116 70823 Fgf2 fibroblast growth factor 2 gene MP:0009974 decreased cerebral cortex pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:9687490 70823 Fgf2 fibroblast growth factor 2 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:19056741 70823 Fgf2 fibroblast growth factor 2 gene MP:0010295 increased eye tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11896616 70823 Fgf2 fibroblast growth factor 2 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:11896616 70823 Fgf2 fibroblast growth factor 2 gene MP:0021186 decreased bone mineral density of vertebrae IAGP N RGD:5509061 20220915 MGI PMID:19056741 70823 Fgf2 fibroblast growth factor 2 gene MP:0021198 abnormal sleep duration IAGP N RGD:5509061 20220922 MGI PMID:11826116 70823 Fgf2 fibroblast growth factor 2 gene MP:0030945 abnormal myoblast migration IAGP N RGD:5509061 20211125 MGI PMID:12917328 70826 Cdk5 cyclin dependent kinase 5 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:8855328 70826 Cdk5 cyclin dependent kinase 5 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11517264 70826 Cdk5 cyclin dependent kinase 5 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:8855328 70826 Cdk5 cyclin dependent kinase 5 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:15067135 70826 Cdk5 cyclin dependent kinase 5 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:11517264 70826 Cdk5 cyclin dependent kinase 5 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11517264 70826 Cdk5 cyclin dependent kinase 5 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8855328 70826 Cdk5 cyclin dependent kinase 5 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:15067135 70826 Cdk5 cyclin dependent kinase 5 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:8855328 70826 Cdk5 cyclin dependent kinase 5 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:15067135 70826 Cdk5 cyclin dependent kinase 5 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11517264 70826 Cdk5 cyclin dependent kinase 5 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8855328 70826 Cdk5 cyclin dependent kinase 5 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:8855328 70826 Cdk5 cyclin dependent kinase 5 gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:8855328 70826 Cdk5 cyclin dependent kinase 5 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:8855328 70826 Cdk5 cyclin dependent kinase 5 gene MP:0001435 absent suckling reflex IAGP N RGD:5509061 20141003 MGI PMID:8855328 70826 Cdk5 cyclin dependent kinase 5 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17529984 70826 Cdk5 cyclin dependent kinase 5 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17529984 70826 Cdk5 cyclin dependent kinase 5 gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:8855328 70826 Cdk5 cyclin dependent kinase 5 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8855328 70826 Cdk5 cyclin dependent kinase 5 gene MP:0001956 hypopnea IAGP N RGD:5509061 20141003 MGI PMID:8855328 70826 Cdk5 cyclin dependent kinase 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15067135 70826 Cdk5 cyclin dependent kinase 5 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17529984 70826 Cdk5 cyclin dependent kinase 5 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:11517264 70826 Cdk5 cyclin dependent kinase 5 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:15067135 70826 Cdk5 cyclin dependent kinase 5 gene MP:0002883 chromatolysis IAGP N RGD:5509061 20141003 MGI PMID:11517264 70826 Cdk5 cyclin dependent kinase 5 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17529984 70826 Cdk5 cyclin dependent kinase 5 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:17529984 70826 Cdk5 cyclin dependent kinase 5 gene MP:0002923 increased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:17529984 70826 Cdk5 cyclin dependent kinase 5 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:8855328 70826 Cdk5 cyclin dependent kinase 5 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:17529984 70826 Cdk5 cyclin dependent kinase 5 gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:8855328 70826 Cdk5 cyclin dependent kinase 5 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11517264 70826 Cdk5 cyclin dependent kinase 5 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8855328 70830 Pld1 phospholipase D1 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23131846 70830 Pld1 phospholipase D1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23109426 70830 Pld1 phospholipase D1 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:20051593 70830 Pld1 phospholipase D1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20231207 MGI 70830 Pld1 phospholipase D1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23131846 70830 Pld1 phospholipase D1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:20051593 70830 Pld1 phospholipase D1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:23131846 70830 Pld1 phospholipase D1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20170413 MGI PMID:22974101 70830 Pld1 phospholipase D1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:23131846 70830 Pld1 phospholipase D1 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:20051593 70830 Pld1 phospholipase D1 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20170413 MGI PMID:22974101 70830 Pld1 phospholipase D1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:20051593 70830 Pld1 phospholipase D1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20170413 MGI PMID:22974101 70830 Pld1 phospholipase D1 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20170413 MGI PMID:22974101 70830 Pld1 phospholipase D1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:21266992 70830 Pld1 phospholipase D1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:20051593 70830 Pld1 phospholipase D1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20051593 70830 Pld1 phospholipase D1 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:23131846 70830 Pld1 phospholipase D1 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:22974101 70832 Cyp51 cytochrome P450, family 51 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0000413 polyphalangy IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0000566 synostosis IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0003807 camptodactyly IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20181101 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0004374 bowed radius IAGP N RGD:5509061 20181101 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0008736 micromelia IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0008817 hematoma IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0009905 absent tongue IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0010196 abnormal lymphatic vessel smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21705796 70832 Cyp51 cytochrome P450, family 51 gene MP:0020301 short tongue IAGP N RGD:5509061 20221027 MGI PMID:21705796 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0000097 short maxilla IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0000120 malocclusion IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0001127 small ovary IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0001263 weight loss IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0002083 premature death IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0004537 abnormal palatine bone horizontal plate morphology IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0011130 absent tertiary ovarian follicles IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0014051 abnormal maxillary-premaxillary suture morphology IAGP N RGD:5509061 20170914 MGI PMID:24565867 7179394 E330023G01Rik RIKEN cDNA E330023G01 gene gene MP:0030082 long lower incisors IAGP N RGD:5509061 20170928 MGI PMID:24565867 7245468 Mirc35hg microRNA cluster 35, host gene gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:23341629 7245468 Mirc35hg microRNA cluster 35, host gene gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23341629 7245468 Mirc35hg microRNA cluster 35, host gene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23341629 7245468 Mirc35hg microRNA cluster 35, host gene gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23341629 7245468 Mirc35hg microRNA cluster 35, host gene gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:23341629 7245468 Mirc35hg microRNA cluster 35, host gene gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:23341629 7245468 Mirc35hg microRNA cluster 35, host gene gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:23341629 7245468 Mirc35hg microRNA cluster 35, host gene gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23341629 7245468 Mirc35hg microRNA cluster 35, host gene gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23341629 7245468 Mirc35hg microRNA cluster 35, host gene gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23341629 7245468 Mirc35hg microRNA cluster 35, host gene gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23341629 7245468 Mirc35hg microRNA cluster 35, host gene gene MP:0005653 phototoxicity IAGP N RGD:5509061 20141003 MGI PMID:23341629 7245468 Mirc35hg microRNA cluster 35, host gene gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:23341629 7245468 Mirc35hg microRNA cluster 35, host gene gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:23341629 7245468 Mirc35hg microRNA cluster 35, host gene gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:23341629 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:14761980 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20160421 MGI PMID:25692702 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12677010 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20220811 MGI 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:12677010 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14761980 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15777864 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:15777864 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:12677010 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22984079 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11544318 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18996151 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0002606 increased basophil cell number IAGP N RGD:5509061 20160421 MGI PMID:25692702 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0003063 increased coping response IAGP N RGD:5509061 20141003 MGI PMID:18996151 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20160804 MGI 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:12677010 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20190815 MGI PMID:29079688 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0008150 decreased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:12677010 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:14761980 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0008156 decreased diameter of tibia IAGP N RGD:5509061 20141003 MGI PMID:14761980 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:11016935 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0008704 abnormal interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:11016935 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0009436 fragmentation of sleep/wake states IAGP N RGD:5509061 20190815 MGI PMID:29079688 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0011396 abnormal sleep behavior IAGP N RGD:5509061 20190815 MGI PMID:29079688 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0011958 increased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:18996151 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0012287 increased frequency of paradoxical sleep IAGP N RGD:5509061 20190815 MGI PMID:29079688 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0012289 abnormal non-rapid eye movement sleep pattern IAGP N RGD:5509061 20190815 MGI PMID:29079688 730815 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 gene MP:0012290 abnormal slow-wave sleep pattern IAGP N RGD:5509061 20190815 MGI PMID:29079688 730818 Adora1 adenosine A1 receptor gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:11470917 730818 Adora1 adenosine A1 receptor gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 730818 Adora1 adenosine A1 receptor gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11470917 730818 Adora1 adenosine A1 receptor gene MP:0002083 premature death IAGP N RGD:5509061 20170119 MGI PMID:27903722 730818 Adora1 adenosine A1 receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12843280 730818 Adora1 adenosine A1 receptor gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11470917 730818 Adora1 adenosine A1 receptor gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12843280 730818 Adora1 adenosine A1 receptor gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20141003 MGI PMID:11470917 730818 Adora1 adenosine A1 receptor gene MP:0002574 increased vertical activity IEA N RGD:5509061 20221215 MGI 730818 Adora1 adenosine A1 receptor gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:11470917 730818 Adora1 adenosine A1 receptor gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:11470917 730818 Adora1 adenosine A1 receptor gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:12843280 730818 Adora1 adenosine A1 receptor gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:11470917 730818 Adora1 adenosine A1 receptor gene MP:0003177 allodynia IAGP N RGD:5509061 20141003 MGI PMID:18940592 730818 Adora1 adenosine A1 receptor gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:15343381 730818 Adora1 adenosine A1 receptor gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 730818 Adora1 adenosine A1 receptor gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11470917 730818 Adora1 adenosine A1 receptor gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:18940592 730818 Adora1 adenosine A1 receptor gene MP:0004041 increased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:17928414 730818 Adora1 adenosine A1 receptor gene MP:0005407 hyperalgesia IAGP N RGD:5509061 20141003 MGI PMID:11470917 730818 Adora1 adenosine A1 receptor gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:17928414 730818 Adora1 adenosine A1 receptor gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 730818 Adora1 adenosine A1 receptor gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20170119 MGI PMID:27903722 730818 Adora1 adenosine A1 receptor gene MP:0011297 absent tubuloglomerular feedback response IAGP N RGD:5509061 20141003 MGI PMID:11504952 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:8662541 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:12198163 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:12782656 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:8662541 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:8698235 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:8698235 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12782656 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8662541 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8698235 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:8698235 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15713637 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:8662541 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:8698235 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0005237 abnormal olfactory tract morphology IAGP N RGD:5509061 20141003 MGI PMID:8698235 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:12782656 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8698235 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8662541 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8698235 730820 Pou3f1 POU domain, class 3, transcription factor 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9242494 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14551157 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:12775562 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000736 delayed muscle development IAGP N RGD:5509061 20141003 MGI PMID:15064723 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15064723 730822 Mmp2 matrix metallopeptidase 2 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:15064723 730822 Mmp2 matrix metallopeptidase 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15064723 730822 Mmp2 matrix metallopeptidase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9278386 730822 Mmp2 matrix metallopeptidase 2 gene MP:0001304 cataract IEA N RGD:5509061 20201022 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12775562 730822 Mmp2 matrix metallopeptidase 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15064723 730822 Mmp2 matrix metallopeptidase 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15064723 730822 Mmp2 matrix metallopeptidase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9278386 730822 Mmp2 matrix metallopeptidase 2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9500469 730822 Mmp2 matrix metallopeptidase 2 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:15522913 730822 Mmp2 matrix metallopeptidase 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9500469 730822 Mmp2 matrix metallopeptidase 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15064723 730822 Mmp2 matrix metallopeptidase 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15618213 730822 Mmp2 matrix metallopeptidase 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:12775562 730822 Mmp2 matrix metallopeptidase 2 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0003434 decreased susceptibility to induced choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:14563686 730822 Mmp2 matrix metallopeptidase 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:9500469 730822 Mmp2 matrix metallopeptidase 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0003840 abnormal coronal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0003841 abnormal lambdoid suture morphology IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0003883 enlarged stomach IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:15522913 730822 Mmp2 matrix metallopeptidase 2 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15064723 730822 Mmp2 matrix metallopeptidase 2 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:14551157 730822 Mmp2 matrix metallopeptidase 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12506102 730822 Mmp2 matrix metallopeptidase 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:9500469 730822 Mmp2 matrix metallopeptidase 2 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:15739229 730822 Mmp2 matrix metallopeptidase 2 gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15064723 730822 Mmp2 matrix metallopeptidase 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:12368215 730822 Mmp2 matrix metallopeptidase 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:15064723 730822 Mmp2 matrix metallopeptidase 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210617 MGI PMID:23144462 730822 Mmp2 matrix metallopeptidase 2 gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:23144462 730822 Mmp2 matrix metallopeptidase 2 gene MP:0009870 abnormal abdominal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:23144462 730822 Mmp2 matrix metallopeptidase 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 730822 Mmp2 matrix metallopeptidase 2 gene MP:0010139 aortitis IAGP N RGD:5509061 20141003 MGI PMID:23144462 730822 Mmp2 matrix metallopeptidase 2 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15064723 730822 Mmp2 matrix metallopeptidase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11747814 730822 Mmp2 matrix metallopeptidase 2 gene MP:0030166 increased inner canthal distance IAGP N RGD:5509061 20171005 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0030189 broad snout IAGP N RGD:5509061 20171019 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0030360 coronal suture sclerosis IAGP N RGD:5509061 20171207 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0030361 lambdoid suture sclerosis IAGP N RGD:5509061 20171207 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0030362 sagittal suture sclerosis IAGP N RGD:5509061 20171207 MGI PMID:17400654 730822 Mmp2 matrix metallopeptidase 2 gene MP:0031274 increased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:23144462 730825 Gnai1 G protein subunit alpha i1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:23236180 730825 Gnai1 G protein subunit alpha i1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 730825 Gnai1 G protein subunit alpha i1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:14715142 730825 Gnai1 G protein subunit alpha i1 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:14715142 730825 Gnai1 G protein subunit alpha i1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:14715142 730825 Gnai1 G protein subunit alpha i1 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:14715142 730825 Gnai1 G protein subunit alpha i1 gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:14715142 730825 Gnai1 G protein subunit alpha i1 gene MP:0002801 abnormal long-term object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:14715142 730825 Gnai1 G protein subunit alpha i1 gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:23236180 730825 Gnai1 G protein subunit alpha i1 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:23236180 730825 Gnai1 G protein subunit alpha i1 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:23236180 730825 Gnai1 G protein subunit alpha i1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15788486 730825 Gnai1 G protein subunit alpha i1 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:15788486 730825 Gnai1 G protein subunit alpha i1 gene MP:0009818 abnormal thromboxane level IAGP N RGD:5509061 20141003 MGI PMID:15788486 730825 Gnai1 G protein subunit alpha i1 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:23236180 730827 Esrra estrogen related receptor, alpha gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:20519122 730827 Esrra estrogen related receptor, alpha gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20519122 730827 Esrra estrogen related receptor, alpha gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23359549 730827 Esrra estrogen related receptor, alpha gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20519122 730827 Esrra estrogen related receptor, alpha gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20519122 730827 Esrra estrogen related receptor, alpha gene MP:0000679 increased percent water in carcass IAGP N RGD:5509061 20141003 MGI PMID:14585956 730827 Esrra estrogen related receptor, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14585956 730827 Esrra estrogen related receptor, alpha gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 730827 Esrra estrogen related receptor, alpha gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 730827 Esrra estrogen related receptor, alpha gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:23359549 730827 Esrra estrogen related receptor, alpha gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14585956 730827 Esrra estrogen related receptor, alpha gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 730827 Esrra estrogen related receptor, alpha gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20211021 MGI 730827 Esrra estrogen related receptor, alpha gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 730827 Esrra estrogen related receptor, alpha gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:20519122 730827 Esrra estrogen related receptor, alpha gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:14585956 730827 Esrra estrogen related receptor, alpha gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:20519122 730827 Esrra estrogen related receptor, alpha gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:20519122 730827 Esrra estrogen related receptor, alpha gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:20519122 730827 Esrra estrogen related receptor, alpha gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20171228 MGI PMID:17229846 730827 Esrra estrogen related receptor, alpha gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:14585956 730827 Esrra estrogen related receptor, alpha gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 730827 Esrra estrogen related receptor, alpha gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:14585956 730827 Esrra estrogen related receptor, alpha gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:14585956 730827 Esrra estrogen related receptor, alpha gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:20519122 730827 Esrra estrogen related receptor, alpha gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20171228 MGI PMID:17229846 730827 Esrra estrogen related receptor, alpha gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:14585956 730827 Esrra estrogen related receptor, alpha gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:14585956 730827 Esrra estrogen related receptor, alpha gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:14585956 730827 Esrra estrogen related receptor, alpha gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:14585956 730827 Esrra estrogen related receptor, alpha gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:20519122 730827 Esrra estrogen related receptor, alpha gene MP:0010052 increased grip strength IEA N RGD:5509061 20181227 MGI 730827 Esrra estrogen related receptor, alpha gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:20519122 730827 Esrra estrogen related receptor, alpha gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20171228 MGI PMID:17229846 730827 Esrra estrogen related receptor, alpha gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20171228 MGI PMID:17229846 730827 Esrra estrogen related receptor, alpha gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20171228 MGI PMID:17229846 730827 Esrra estrogen related receptor, alpha gene MP:0011954 shortened PQ interval IEA N RGD:5509061 20211021 MGI 730827 Esrra estrogen related receptor, alpha gene MP:0014396 decreased fat cell mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:17229846 730829 Retn resistin gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19188682 730829 Retn resistin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19188682 730829 Retn resistin gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:19188682 730829 Retn resistin gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:14976316 730829 Retn resistin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19188682 730829 Retn resistin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:19188682 730829 Retn resistin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:14976316 730829 Retn resistin gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:19188682 730829 Retn resistin gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14976316 730829 Retn resistin gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:19188682 730829 Retn resistin gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240418 MGI PMID:19188682 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:14975238 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17510322 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14975238 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:14975238 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:10490101 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11481489 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:11481489 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:14975238 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17510322 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:10490101 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15208705 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14975238 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10490101 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11481489 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:12754505 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:11481489 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:11481489 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:16517610 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:14975238 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:14975238 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:14975238 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12754505 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14975238 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12754505 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:17510322 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12754505 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15208705 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15208705 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15208705 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15220914 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10490101 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:11481489 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:14975238 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:17510322 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:10490101 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14975238 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15208705 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15220914 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:15208705 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15220914 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15220914 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:14975238 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:12591901 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12754507 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11481489 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17510322 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10490101 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:11481489 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:12754505 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15220914 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11481489 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12754505 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10490101 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10490101 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:11481489 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0012100 absent spongiotrophoblast IAGP N RGD:5509061 20141003 MGI PMID:12754505 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20160407 MGI PMID:15208705 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0014440 increased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:15208705 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0014440 increased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:15220914 730834 Socs3 suppressor of cytokine signaling 3 gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20191219 MGI PMID:11481489 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:17641092 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:17641092 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:22851578 730835 Akr1b7 aldo-keto reductase family 1, member B7 gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:22851578 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10036240 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:16814771 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24578301 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:10036240 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:10036240 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:22295099 730839 Cspg4 chondroitin sulfate proteoglycan 4 gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20141003 MGI PMID:22295099 730842 Nnat neuronatin gene MP:0000274 enlarged heart IEA N RGD:5509061 20201022 MGI 730842 Nnat neuronatin gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 730842 Nnat neuronatin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20210617 MGI PMID:29864031 730842 Nnat neuronatin gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 730842 Nnat neuronatin gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 730842 Nnat neuronatin gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20210617 MGI PMID:29864031 730842 Nnat neuronatin gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20210617 MGI PMID:29864031 730842 Nnat neuronatin gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 730842 Nnat neuronatin gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20210617 MGI PMID:29864031 730842 Nnat neuronatin gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20210617 MGI PMID:29864031 730842 Nnat neuronatin gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210617 MGI PMID:29864031 730842 Nnat neuronatin gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 730842 Nnat neuronatin gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20210617 MGI PMID:29864031 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:10716933 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10716933 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:12556477 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10716933 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10716933 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10716933 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12556477 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:10716933 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:12556477 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10716933 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10716933 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:10716933 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12556477 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:10716933 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10716933 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10716933 730843 Mafk v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:10716933 730847 Casp8 caspase 8 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12404118 730847 Casp8 caspase 8 gene MP:0000274 enlarged heart IEA N RGD:5509061 20240523 MGI 730847 Casp8 caspase 8 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15322156 730847 Casp8 caspase 8 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:9729047 730847 Casp8 caspase 8 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20478530 730847 Casp8 caspase 8 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20150326 MGI PMID:21878202 730847 Casp8 caspase 8 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20150326 MGI PMID:21878202 730847 Casp8 caspase 8 gene MP:0000601 small liver IEA N RGD:5509061 20141003 MGI 730847 Casp8 caspase 8 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20170713 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21368763 730847 Casp8 caspase 8 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20150219 MGI PMID:24557836 730847 Casp8 caspase 8 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16148088 730847 Casp8 caspase 8 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21368763 730847 Casp8 caspase 8 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20150219 MGI PMID:24557836 730847 Casp8 caspase 8 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20220407 MGI PMID:34625556 730847 Casp8 caspase 8 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:21368763 730847 Casp8 caspase 8 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:15322156 730847 Casp8 caspase 8 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0001192 scaly skin IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0001212 skin lesions IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150326 MGI PMID:21878202 730847 Casp8 caspase 8 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20150326 MGI PMID:21878202 730847 Casp8 caspase 8 gene MP:0001606 impaired hematopoiesis IEA N RGD:5509061 20141003 MGI 730847 Casp8 caspase 8 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20150326 MGI PMID:21878202 730847 Casp8 caspase 8 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:20478530 730847 Casp8 caspase 8 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9729047 730847 Casp8 caspase 8 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:15322156 730847 Casp8 caspase 8 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:12404118 730847 Casp8 caspase 8 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20478530 730847 Casp8 caspase 8 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:15322156 730847 Casp8 caspase 8 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20150326 MGI PMID:21878202 730847 Casp8 caspase 8 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:9729047 730847 Casp8 caspase 8 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16245150 730847 Casp8 caspase 8 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:9729047 730847 Casp8 caspase 8 gene MP:0002220 large lymphoid organs IAGP N RGD:5509061 20141003 MGI PMID:21368763 730847 Casp8 caspase 8 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:9729047 730847 Casp8 caspase 8 gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:15322156 730847 Casp8 caspase 8 gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:16148088 730847 Casp8 caspase 8 gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:9729047 730847 Casp8 caspase 8 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16148088 730847 Casp8 caspase 8 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:9729047 730847 Casp8 caspase 8 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:20478530 730847 Casp8 caspase 8 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20478530 730847 Casp8 caspase 8 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20150326 MGI PMID:21878202 730847 Casp8 caspase 8 gene MP:0002989 small kidney IEA N RGD:5509061 20240523 MGI 730847 Casp8 caspase 8 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9729047 730847 Casp8 caspase 8 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12404118 730847 Casp8 caspase 8 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16245150 730847 Casp8 caspase 8 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16245150 730847 Casp8 caspase 8 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20180125 MGI PMID:15322156 730847 Casp8 caspase 8 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20141003 MGI PMID:20478530 730847 Casp8 caspase 8 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20150326 MGI PMID:21878202 730847 Casp8 caspase 8 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12404118 730847 Casp8 caspase 8 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:12404118 730847 Casp8 caspase 8 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:15322156 730847 Casp8 caspase 8 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:12654726 730847 Casp8 caspase 8 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:12404118 730847 Casp8 caspase 8 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12654726 730847 Casp8 caspase 8 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20150326 MGI PMID:21878202 730847 Casp8 caspase 8 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16148088 730847 Casp8 caspase 8 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21368763 730847 Casp8 caspase 8 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20150219 MGI PMID:24557836 730847 Casp8 caspase 8 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16148088 730847 Casp8 caspase 8 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12654726 730847 Casp8 caspase 8 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0005083 abnormal biliary tract morphology IAGP N RGD:5509061 20150326 MGI PMID:21878202 730847 Casp8 caspase 8 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16148088 730847 Casp8 caspase 8 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16157684 730847 Casp8 caspase 8 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12654726 730847 Casp8 caspase 8 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20150326 MGI PMID:21878202 730847 Casp8 caspase 8 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20150326 MGI PMID:21878202 730847 Casp8 caspase 8 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:12404118 730847 Casp8 caspase 8 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:16245150 730847 Casp8 caspase 8 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9729047 730847 Casp8 caspase 8 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9729047 730847 Casp8 caspase 8 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20478530 730847 Casp8 caspase 8 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:20478530 730847 Casp8 caspase 8 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20150326 MGI PMID:21878202 730847 Casp8 caspase 8 gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20150326 MGI PMID:21878202 730847 Casp8 caspase 8 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16148088 730847 Casp8 caspase 8 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:15322156 730847 Casp8 caspase 8 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12654726 730847 Casp8 caspase 8 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12654726 730847 Casp8 caspase 8 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12654726 730847 Casp8 caspase 8 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 730847 Casp8 caspase 8 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12654726 730847 Casp8 caspase 8 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20141003 MGI PMID:15322156 730847 Casp8 caspase 8 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16148088 730847 Casp8 caspase 8 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0008542 enlarged cervical lymph nodes IAGP N RGD:5509061 20170713 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0008891 decreased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21368763 730847 Casp8 caspase 8 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21368763 730847 Casp8 caspase 8 gene MP:0009631 enlarged axillary lymph nodes IAGP N RGD:5509061 20170713 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15322156 730847 Casp8 caspase 8 gene MP:0009795 epidermal spongiosis IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0010017 visceral vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15322156 730847 Casp8 caspase 8 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 730847 Casp8 caspase 8 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 730847 Casp8 caspase 8 gene MP:0011081 decreased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9729047 730847 Casp8 caspase 8 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12654726 730847 Casp8 caspase 8 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9729047 730847 Casp8 caspase 8 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20150219 MGI PMID:24557836 730847 Casp8 caspase 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12404118 730847 Casp8 caspase 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15322156 730847 Casp8 caspase 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16245150 730847 Casp8 caspase 8 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20150219 MGI PMID:24557836 730847 Casp8 caspase 8 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9729047 730847 Casp8 caspase 8 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 730847 Casp8 caspase 8 gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20141003 MGI PMID:21368762 730847 Casp8 caspase 8 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20240523 MGI 730847 Casp8 caspase 8 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 730847 Casp8 caspase 8 gene MP:0013648 increased CD11b-high dendritic cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 730847 Casp8 caspase 8 gene MP:0014273 abnormal skin vasculature morphology IAGP N RGD:5509061 20230810 MGI PMID:21135236 730847 Casp8 caspase 8 gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:15322156 730850 Pax8 paired box 8 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:17376978 730850 Pax8 paired box 8 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0000054 delayed ear emergence IAGP N RGD:5509061 20160623 MGI PMID:25127920 730850 Pax8 paired box 8 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20151112 MGI PMID:17932107 730850 Pax8 paired box 8 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20151112 MGI PMID:17932107 730850 Pax8 paired box 8 gene MP:0000231 hypertension IAGP N RGD:5509061 20200310 MGI PMID:31673025 730850 Pax8 paired box 8 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:21354128 730850 Pax8 paired box 8 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:12435636 730850 Pax8 paired box 8 gene MP:0000547 short limbs IAGP N RGD:5509061 20151112 MGI PMID:17932107 730850 Pax8 paired box 8 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9590297 730850 Pax8 paired box 8 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20160623 MGI PMID:25127920 730850 Pax8 paired box 8 gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17082261 730850 Pax8 paired box 8 gene MP:0001136 dilated uterine cervix IAGP N RGD:5509061 20141003 MGI PMID:17082261 730850 Pax8 paired box 8 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:12435636 730850 Pax8 paired box 8 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:17082261 730850 Pax8 paired box 8 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17210747 730850 Pax8 paired box 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160623 MGI PMID:25127920 730850 Pax8 paired box 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160623 MGI PMID:25127920 730850 Pax8 paired box 8 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20160623 MGI PMID:25127920 730850 Pax8 paired box 8 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12435636 730850 Pax8 paired box 8 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9590297 730850 Pax8 paired box 8 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20200310 MGI PMID:31673025 730850 Pax8 paired box 8 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:23716689 730850 Pax8 paired box 8 gene MP:0001762 polyuria IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0001762 polyuria IAGP N RGD:5509061 20200310 MGI PMID:31673025 730850 Pax8 paired box 8 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12435636 730850 Pax8 paired box 8 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17210747 730850 Pax8 paired box 8 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17082261 730850 Pax8 paired box 8 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9590297 730850 Pax8 paired box 8 gene MP:0002083 premature death IAGP N RGD:5509061 20160623 MGI PMID:25127920 730850 Pax8 paired box 8 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25127920 730850 Pax8 paired box 8 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:17210747 730850 Pax8 paired box 8 gene MP:0002661 abnormal corpus epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:17210747 730850 Pax8 paired box 8 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:31673025 730850 Pax8 paired box 8 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0002827 abnormal renal corpuscle morphology IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0002871 albuminuria IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0002871 albuminuria IAGP N RGD:5509061 20200310 MGI PMID:31673025 730850 Pax8 paired box 8 gene MP:0002902 decreased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:21354128 730850 Pax8 paired box 8 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:9590297 730850 Pax8 paired box 8 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20160623 MGI PMID:25127920 730850 Pax8 paired box 8 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0002963 decreased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:21354128 730850 Pax8 paired box 8 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20151112 MGI PMID:17932107 730850 Pax8 paired box 8 gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:21354128 730850 Pax8 paired box 8 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:17210747 730850 Pax8 paired box 8 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20200310 MGI PMID:31673025 730850 Pax8 paired box 8 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20151112 MGI PMID:17932107 730850 Pax8 paired box 8 gene MP:0003421 abnormal thyroid gland development IAGP N RGD:5509061 20141003 MGI PMID:9590297 730850 Pax8 paired box 8 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12435636 730850 Pax8 paired box 8 gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20160623 MGI PMID:25127920 730850 Pax8 paired box 8 gene MP:0003534 blind vagina IAGP N RGD:5509061 20141003 MGI PMID:12435636 730850 Pax8 paired box 8 gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:12435636 730850 Pax8 paired box 8 gene MP:0003572 abnormal uterus development IAGP N RGD:5509061 20141003 MGI PMID:17082261 730850 Pax8 paired box 8 gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:21354128 730850 Pax8 paired box 8 gene MP:0003670 dilated renal glomerular capsule IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:12435636 730850 Pax8 paired box 8 gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0003826 abnormal Mullerian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:17082261 730850 Pax8 paired box 8 gene MP:0003870 decreased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:21354128 730850 Pax8 paired box 8 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0004041 increased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20161201 MGI PMID:25892012 730850 Pax8 paired box 8 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:17210747 730850 Pax8 paired box 8 gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:23716689 730850 Pax8 paired box 8 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17376978 730850 Pax8 paired box 8 gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17376979 730850 Pax8 paired box 8 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:12435636 730850 Pax8 paired box 8 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0004562 abnormal inner hair cell synaptic ribbon morphology IAGP N RGD:5509061 20141003 MGI PMID:17376978 730850 Pax8 paired box 8 gene MP:0004591 enlarged tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0004633 abnormal cochlear IHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17376978 730850 Pax8 paired box 8 gene MP:0004660 absent thyroid follicular cells IAGP N RGD:5509061 20141003 MGI PMID:9590297 730850 Pax8 paired box 8 gene MP:0004662 abnormal thyroid diverticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:9590297 730850 Pax8 paired box 8 gene MP:0004664 delayed inner ear development IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0004665 abnormal stapedial artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0004666 absent stapedial artery IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20160623 MGI PMID:25127920 730850 Pax8 paired box 8 gene MP:0004697 abnormal thyroid follicular cell morphology IAGP N RGD:5509061 20160623 MGI PMID:25127920 730850 Pax8 paired box 8 gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:17210747 730850 Pax8 paired box 8 gene MP:0004729 absent efferent ductules of testis IAGP N RGD:5509061 20141003 MGI PMID:17210747 730850 Pax8 paired box 8 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:31673025 730850 Pax8 paired box 8 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17210747 730850 Pax8 paired box 8 gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:17210747 730850 Pax8 paired box 8 gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17210747 730850 Pax8 paired box 8 gene MP:0004969 pale kidney IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:9590297 730850 Pax8 paired box 8 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20160623 MGI PMID:25127920 730850 Pax8 paired box 8 gene MP:0005135 increased thyroid-stimulating hormone level IAGP N RGD:5509061 20151112 MGI PMID:17932107 730850 Pax8 paired box 8 gene MP:0005314 absent thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:12435636 730850 Pax8 paired box 8 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:17376978 730850 Pax8 paired box 8 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:17376979 730850 Pax8 paired box 8 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:21354128 730850 Pax8 paired box 8 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:9590297 730850 Pax8 paired box 8 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20160623 MGI PMID:25127920 730850 Pax8 paired box 8 gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:21354128 730850 Pax8 paired box 8 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:23716689 730850 Pax8 paired box 8 gene MP:0006033 abnormal external auditory canal morphology IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21924257 730850 Pax8 paired box 8 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20160623 MGI PMID:25127920 730850 Pax8 paired box 8 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20200310 MGI PMID:31673025 730850 Pax8 paired box 8 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:21354128 730850 Pax8 paired box 8 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20151112 MGI PMID:17932107 730850 Pax8 paired box 8 gene MP:0008257 thin myometrium IAGP N RGD:5509061 20141003 MGI PMID:17082261 730850 Pax8 paired box 8 gene MP:0008329 decreased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:17210747 730850 Pax8 paired box 8 gene MP:0008332 decreased lactotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:17210747 730850 Pax8 paired box 8 gene MP:0008337 increased thyrotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:17210747 730850 Pax8 paired box 8 gene MP:0009069 dilated oviduct IAGP N RGD:5509061 20141003 MGI PMID:17082261 730850 Pax8 paired box 8 gene MP:0009215 absent uterine horn IAGP N RGD:5509061 20141003 MGI PMID:17082261 730850 Pax8 paired box 8 gene MP:0009224 absent endometrium IAGP N RGD:5509061 20141003 MGI PMID:17082261 730850 Pax8 paired box 8 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:23716689 730850 Pax8 paired box 8 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20161201 MGI PMID:25892012 730850 Pax8 paired box 8 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23716689 730850 Pax8 paired box 8 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20200310 MGI PMID:31673025 730850 Pax8 paired box 8 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20151112 MGI PMID:17932107 730850 Pax8 paired box 8 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20151112 MGI PMID:17932107 730850 Pax8 paired box 8 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:12435636 730850 Pax8 paired box 8 gene MP:0011060 abnormal kinocilium morphology IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0011066 abnormal renal tubule epithelial cell primary cilium morphology IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12435636 730850 Pax8 paired box 8 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17082261 730850 Pax8 paired box 8 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:12435636 730850 Pax8 paired box 8 gene MP:0011365 small metanephros IAGP N RGD:5509061 20141003 MGI PMID:12435636 730850 Pax8 paired box 8 gene MP:0011366 absent metanephros IAGP N RGD:5509061 20141003 MGI PMID:12435636 730850 Pax8 paired box 8 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21354128 730850 Pax8 paired box 8 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:21354128 730850 Pax8 paired box 8 gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:21354128 730850 Pax8 paired box 8 gene MP:0011736 decreased urine ammonia level IAGP N RGD:5509061 20141003 MGI PMID:23716689 730850 Pax8 paired box 8 gene MP:0011843 abnormal kidney collecting duct epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21354128 730850 Pax8 paired box 8 gene MP:0011846 decreased kidney collecting duct number IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0011858 elongated kidney papilla IAGP N RGD:5509061 20141003 MGI PMID:21354128 730850 Pax8 paired box 8 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20170921 MGI PMID:23716689 730850 Pax8 paired box 8 gene MP:0013305 isosthenuria IAGP N RGD:5509061 20160929 MGI PMID:25799508 730850 Pax8 paired box 8 gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20151112 MGI PMID:17932107 730850 Pax8 paired box 8 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20151112 MGI PMID:17932107 730850 Pax8 paired box 8 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:17932107 730850 Pax8 paired box 8 gene MP:0021184 decreased bone mineral density of humerus IAGP N RGD:5509061 20220915 MGI PMID:17932107 730850 Pax8 paired box 8 gene MP:0030160 abnormal auditory bulla morphology IAGP N RGD:5509061 20171207 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0030407 abnormal stapes crus morpholgy IAGP N RGD:5509061 20171207 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0030411 decreased round window size IAGP N RGD:5509061 20171207 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0030412 absent round window IAGP N RGD:5509061 20171207 MGI PMID:14981357 730850 Pax8 paired box 8 gene MP:0031229 increased angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:31673025 730850 Pax8 paired box 8 gene MP:0031285 external auditory canal stenosis IAGP N RGD:5509061 20211014 MGI PMID:14981357 730852 Crhbp corticotropin releasing hormone binding protein gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10500222 730852 Crhbp corticotropin releasing hormone binding protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10500222 730852 Crhbp corticotropin releasing hormone binding protein gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:10500222 730852 Crhbp corticotropin releasing hormone binding protein gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:10500222 730857 Cald1 caldesmon 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:15823561 730857 Cald1 caldesmon 1 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:23986516 730857 Cald1 caldesmon 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15823561 730857 Cald1 caldesmon 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23986516 730857 Cald1 caldesmon 1 gene MP:0011774 abnormal urinary bladder detrusor smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23986516 730857 Cald1 caldesmon 1 gene MP:0011799 increased urinary bladder weight IAGP N RGD:5509061 20141003 MGI PMID:23986516 730860 Psmc3ip proteasome (prosome, macropain) 26S subunit, ATPase 3, interacting protein gene MP:0001117 absent gametes IAGP N RGD:5509061 20141003 MGI PMID:14667414 730860 Psmc3ip proteasome (prosome, macropain) 26S subunit, ATPase 3, interacting protein gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:14667414 730860 Psmc3ip proteasome (prosome, macropain) 26S subunit, ATPase 3, interacting protein gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:14667414 730860 Psmc3ip proteasome (prosome, macropain) 26S subunit, ATPase 3, interacting protein gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14667414 730860 Psmc3ip proteasome (prosome, macropain) 26S subunit, ATPase 3, interacting protein gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:14667414 730860 Psmc3ip proteasome (prosome, macropain) 26S subunit, ATPase 3, interacting protein gene MP:0003582 abnormal ovary development IAGP N RGD:5509061 20141003 MGI PMID:14667414 730860 Psmc3ip proteasome (prosome, macropain) 26S subunit, ATPase 3, interacting protein gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:14667414 730860 Psmc3ip proteasome (prosome, macropain) 26S subunit, ATPase 3, interacting protein gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:23318132 730860 Psmc3ip proteasome (prosome, macropain) 26S subunit, ATPase 3, interacting protein gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:24304900 730860 Psmc3ip proteasome (prosome, macropain) 26S subunit, ATPase 3, interacting protein gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:14667414 730860 Psmc3ip proteasome (prosome, macropain) 26S subunit, ATPase 3, interacting protein gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:23870400 730860 Psmc3ip proteasome (prosome, macropain) 26S subunit, ATPase 3, interacting protein gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:24304900 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22822162 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:16705176 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22822162 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0001668 abnormal intestinal fructose absorption IAGP N RGD:5509061 20141003 MGI PMID:22822162 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22822162 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:22822162 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22822162 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220714 MGI PMID:18428038 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:16705176 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:18428038 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22822162 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22822162 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22822162 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22822162 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16705176 730863 Slc2a8 solute carrier family 2, (facilitated glucose transporter), member 8 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18428038 730865 Sdc1 syndecan 1 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12414997 730865 Sdc1 syndecan 1 gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10888884 730865 Sdc1 syndecan 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230119 MGI 730865 Sdc1 syndecan 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12414997 730865 Sdc1 syndecan 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10888884 730865 Sdc1 syndecan 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11333985 730865 Sdc1 syndecan 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16299282 730865 Sdc1 syndecan 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 730865 Sdc1 syndecan 1 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:12414997 730865 Sdc1 syndecan 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:16495570 730865 Sdc1 syndecan 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230119 MGI 730865 Sdc1 syndecan 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20230119 MGI 730865 Sdc1 syndecan 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230119 MGI 730865 Sdc1 syndecan 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16495570 730865 Sdc1 syndecan 1 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:16495570 730865 Sdc1 syndecan 1 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:16495570 730865 Sdc1 syndecan 1 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16299282 730865 Sdc1 syndecan 1 gene MP:0020861 abnormal cornea wound healing IAGP N RGD:5509061 20181101 MGI PMID:12414997 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:18418378 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:18268011 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:18268011 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:18418378 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:18418378 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18418378 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18418378 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:18212066 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0003364 increased insulinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18418378 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:18418378 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:18418378 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18212066 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18268011 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18212066 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18212066 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18268011 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18268011 730867 Rgs5 regulator of G-protein signaling 5 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:18418378 730869 Slc15a1 solute carrier family 15 (oligopeptide transporter), member 1 gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:19434858 730883 Plin2 perilipin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 730883 Plin2 perilipin 2 gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16428458 730883 Plin2 perilipin 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0002991 abnormal sebaceous gland physiology IAGP N RGD:5509061 20150813 MGI PMID:23688400 730883 Plin2 perilipin 2 gene MP:0003011 delayed dark adaptation IAGP N RGD:5509061 20141003 MGI PMID:18606814 730883 Plin2 perilipin 2 gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:17921437 730883 Plin2 perilipin 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18606814 730883 Plin2 perilipin 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0008779 abnormal maternal behavior IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16428458 730883 Plin2 perilipin 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0011233 abnormal vitamin A metabolism IAGP N RGD:5509061 20141003 MGI PMID:18606814 730883 Plin2 perilipin 2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:23402988 730883 Plin2 perilipin 2 gene MP:0012725 small sebaceous gland IAGP N RGD:5509061 20150813 MGI PMID:23688400 730883 Plin2 perilipin 2 gene MP:0013193 sebaceous gland hypoplasia IAGP N RGD:5509061 20150813 MGI PMID:23688400 730883 Plin2 perilipin 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:16428458 730883 Plin2 perilipin 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:23402988 730885 Abo ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210520 MGI 730885 Abo ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase gene MP:0001147 small testis IEA N RGD:5509061 20210520 MGI 730885 Abo ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17376811 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:17376811 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0001017 abnormal stellate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17376811 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21333348 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:21408140 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:7923378 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:7923378 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0001468 abnormal temporal memory IAGP N RGD:5509061 20141003 MGI PMID:7923378 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:7923378 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:7923378 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11865068 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:11865068 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20141003 MGI PMID:11865068 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8202542 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11865068 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:7923378 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:11865068 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21333348 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:8662559 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:21333348 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:11865068 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17376811 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:20837544 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:21408140 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:11865068 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0003695 delayed blastocyst hatching from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:11865068 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21408140 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:19041748 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:21408140 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21333348 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:21333348 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:21333348 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:11865068 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:11865068 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:11865068 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:21408140 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:8202542 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:21931825 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:8662559 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0009776 decreased behavioral withdrawal response IAGP N RGD:5509061 20141003 MGI PMID:8662559 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0010887 pale lung IAGP N RGD:5509061 20141003 MGI PMID:21408140 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11865068 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11865068 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21408140 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:19041748 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:11970866 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0030947 increased myoblast proliferation IAGP N RGD:5509061 20190725 MGI PMID:21931825 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0030957 abnormal myotube morphology IAGP N RGD:5509061 20190725 MGI PMID:21931825 730887 Creb1 cAMP responsive element binding protein 1 gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:21931825 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0000691 enlarged spleen IEA N RGD:5509061 20170105 MGI 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17671657 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17671657 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12511592 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12511592 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12511592 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16455782 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16455782 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12511592 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14573616 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:12511592 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:16455782 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20200820 MGI PMID:29570986 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12511592 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21124450 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:17671657 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:17671657 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16455782 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12511592 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:14573616 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16455782 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16455782 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12511592 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12511592 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17671657 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16455782 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17671657 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12511592 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16455782 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20141003 MGI PMID:21124450 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17671657 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20191226 MGI PMID:12511592 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20191226 MGI PMID:14573616 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0011478 abnormal urine catecholamine level IAGP N RGD:5509061 20141003 MGI PMID:12511592 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0011958 increased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:17671657 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:16455782 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:14573616 730889 Prkaa2 protein kinase, AMP-activated, alpha 2 catalytic subunit gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:14573616 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:19037247 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19052228 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0000348 abnormal aerobic fitness IAGP N RGD:5509061 20141003 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19037247 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141030 MGI PMID:21239618 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19037247 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19037247 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:19037247 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0002596 abnormal hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:24268577 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141030 MGI PMID:21239618 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19037247 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20141003 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20141003 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:21228185 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141030 MGI PMID:21239618 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141030 MGI PMID:21239618 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141030 MGI PMID:21239618 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0003948 abnormal gas homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141030 MGI PMID:21239618 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19037247 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141030 MGI PMID:21239618 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141030 MGI PMID:21239618 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:19037247 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0005469 abnormal thyroxine level IAGP N RGD:5509061 20141030 MGI PMID:21239618 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:19052228 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141030 MGI PMID:21239618 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141030 MGI PMID:21239618 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19037247 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:19037247 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19037247 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19037247 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17928865 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141030 MGI PMID:21239618 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0010225 abnormal quadriceps morphology IAGP N RGD:5509061 20141003 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:24268577 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:19037247 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0012107 enhanced exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0014344 abnormal skeletal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0014368 enhanced long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:21228185 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:19037247 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20180125 MGI PMID:22078881 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:11030619 730891 Ncor1 nuclear receptor co-repressor 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22078881 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:9359707 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:9359707 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:9359707 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:11160181 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20160922 MGI PMID:24652767 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001191 abnormal skin condition IEA N RGD:5509061 20160804 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:15199130 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20160804 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20160804 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9359707 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:11869686 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:7834752 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001805 decreased IgG level IEA N RGD:5509061 20150122 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:8598461 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:7834752 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20160922 MGI PMID:24652767 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20160804 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7834752 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12904583 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002221 abnormal lymph organ size IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002353 abnormal inguinal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:19060899 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14568969 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12055593 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:12055593 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002392 abnormal Peyer's patch T cell area morphology IAGP N RGD:5509061 20141003 MGI PMID:12055593 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11160181 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:7834752 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20160922 MGI PMID:24652767 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:14568969 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14568969 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16973390 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:7834752 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:7834752 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:16571762 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20160922 MGI PMID:24652767 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:12235116 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:9359707 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9359707 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:11160181 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:11160181 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9359707 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:9359707 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160804 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0003998 decreased thermal nociceptive threshold IEA N RGD:5509061 20160804 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16571762 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16571762 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0004417 decreased cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:16571762 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0004597 increased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20141003 MGI PMID:16571762 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:16571762 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:14568969 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:16973390 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:8598461 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19060899 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0004978 decreased B-1 B cell number IEA N RGD:5509061 20181011 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:9359707 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:11160181 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005046 absent spleen white pulp IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7834752 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8598461 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19060899 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:9359707 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14568969 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20160804 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14568969 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:19060899 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19060899 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11869686 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008122 decreased myeloid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:12055593 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:11869686 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:12055593 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12055593 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008168 decreased B-1a cell number IEA N RGD:5509061 20190404 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:11034607 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16973390 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:16973390 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:16973390 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:9359707 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:9407039 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:7834752 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20160922 MGI PMID:24652767 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20180215 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22733995 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008600 decreased circulating interleukin-2 level IAGP N RGD:5509061 20141003 MGI PMID:19060899 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008648 decreased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:22733995 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008658 decreased interleukin-1 beta secretion IEA N RGD:5509061 20190404 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:11869686 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:22733995 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:7834752 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:9359707 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20160804 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20141003 MGI PMID:11160181 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19060899 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0009624 small inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19060899 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:7834752 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20160922 MGI PMID:24652767 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0010842 decreased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0010845 decreased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7590249 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15199130 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15199130 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9529315 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20150108 MGI 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0030505 tooth impaction IAGP N RGD:5509061 20191219 MGI PMID:9359707 730893 Nfkb1 nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105 gene MP:0031039 decreased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:7834752 730895 Il18 interleukin 18 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17578927 730895 Il18 interleukin 18 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17433555 730895 Il18 interleukin 18 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23219391 730895 Il18 interleukin 18 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16959946 730895 Il18 interleukin 18 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:17578927 730895 Il18 interleukin 18 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23219391 730895 Il18 interleukin 18 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:23219391 730895 Il18 interleukin 18 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:16959946 730895 Il18 interleukin 18 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23219391 730895 Il18 interleukin 18 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18573894 730895 Il18 interleukin 18 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10453027 730895 Il18 interleukin 18 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16861683 730895 Il18 interleukin 18 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17664259 730895 Il18 interleukin 18 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16861683 730895 Il18 interleukin 18 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12151598 730895 Il18 interleukin 18 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15122309 730895 Il18 interleukin 18 gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:17578927 730895 Il18 interleukin 18 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17250807 730895 Il18 interleukin 18 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18573894 730895 Il18 interleukin 18 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:17578927 730895 Il18 interleukin 18 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:10453027 730895 Il18 interleukin 18 gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:10453027 730895 Il18 interleukin 18 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:9529155 730895 Il18 interleukin 18 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17578927 730895 Il18 interleukin 18 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18573894 730895 Il18 interleukin 18 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17578927 730895 Il18 interleukin 18 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:9529155 730895 Il18 interleukin 18 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:12122053 730895 Il18 interleukin 18 gene MP:0006185 retina hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15122309 730895 Il18 interleukin 18 gene MP:0008002 hyperchlorhydria IAGP N RGD:5509061 20141003 MGI PMID:16959946 730895 Il18 interleukin 18 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10816504 730895 Il18 interleukin 18 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:18573894 730895 Il18 interleukin 18 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:18573894 730895 Il18 interleukin 18 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12151598 730895 Il18 interleukin 18 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:21565393 730895 Il18 interleukin 18 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:10816504 730895 Il18 interleukin 18 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18573894 730895 Il18 interleukin 18 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18573894 730895 Il18 interleukin 18 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9529155 730895 Il18 interleukin 18 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:10816504 730895 Il18 interleukin 18 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:18573894 730895 Il18 interleukin 18 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:9529155 730895 Il18 interleukin 18 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18573894 730895 Il18 interleukin 18 gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:10816504 730895 Il18 interleukin 18 gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:17578927 730895 Il18 interleukin 18 gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:18573894 730895 Il18 interleukin 18 gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:9529155 730895 Il18 interleukin 18 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18573894 730895 Il18 interleukin 18 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17664259 730895 Il18 interleukin 18 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:10816504 730895 Il18 interleukin 18 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:10453027 730895 Il18 interleukin 18 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:10453027 730895 Il18 interleukin 18 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:10453027 730895 Il18 interleukin 18 gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17578927 730895 Il18 interleukin 18 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20141003 MGI PMID:21565393 730895 Il18 interleukin 18 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:17250807 730897 Hnrnpab heterogeneous nuclear ribonucleoprotein A/B gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 730897 Hnrnpab heterogeneous nuclear ribonucleoprotein A/B gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20160526 MGI PMID:22332140 730897 Hnrnpab heterogeneous nuclear ribonucleoprotein A/B gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20160526 MGI PMID:22332140 730897 Hnrnpab heterogeneous nuclear ribonucleoprotein A/B gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 730897 Hnrnpab heterogeneous nuclear ribonucleoprotein A/B gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20160526 MGI PMID:22332140 730897 Hnrnpab heterogeneous nuclear ribonucleoprotein A/B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 730899 Ereg epiregulin gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:15456865 730899 Ereg epiregulin gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:15365177 730899 Ereg epiregulin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15456865 730899 Ereg epiregulin gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15456865 730899 Ereg epiregulin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15456865 730899 Ereg epiregulin gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15456865 730899 Ereg epiregulin gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:15456865 730899 Ereg epiregulin gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15456865 730904 Ccnd2 cyclin D2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12502747 730904 Ccnd2 cyclin D2 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:12502747 730904 Ccnd2 cyclin D2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15315760 730904 Ccnd2 cyclin D2 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:15315760 730904 Ccnd2 cyclin D2 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20201022 MGI 730904 Ccnd2 cyclin D2 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:12502747 730904 Ccnd2 cyclin D2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10101126 730904 Ccnd2 cyclin D2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:10101126 730904 Ccnd2 cyclin D2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:12502747 730904 Ccnd2 cyclin D2 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:16413468 730904 Ccnd2 cyclin D2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:10101126 730904 Ccnd2 cyclin D2 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10101126 730904 Ccnd2 cyclin D2 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:10101126 730904 Ccnd2 cyclin D2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10101126 730904 Ccnd2 cyclin D2 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:12502747 730904 Ccnd2 cyclin D2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10101126 730904 Ccnd2 cyclin D2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12502747 730904 Ccnd2 cyclin D2 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:10101126 730904 Ccnd2 cyclin D2 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:8945475 730904 Ccnd2 cyclin D2 gene MP:0001147 small testis IEA N RGD:5509061 20200402 MGI 730904 Ccnd2 cyclin D2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 730904 Ccnd2 cyclin D2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12502747 730904 Ccnd2 cyclin D2 gene MP:0001512 trunk curl IEA N RGD:5509061 20200402 MGI 730904 Ccnd2 cyclin D2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 730904 Ccnd2 cyclin D2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15315760 730904 Ccnd2 cyclin D2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8945475 730904 Ccnd2 cyclin D2 gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20141003 MGI PMID:8945475 730904 Ccnd2 cyclin D2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12502747 730904 Ccnd2 cyclin D2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15315760 730904 Ccnd2 cyclin D2 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:15315760 730904 Ccnd2 cyclin D2 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15315760 730904 Ccnd2 cyclin D2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20200402 MGI 730904 Ccnd2 cyclin D2 gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12502747 730904 Ccnd2 cyclin D2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8945475 730904 Ccnd2 cyclin D2 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:12502747 730904 Ccnd2 cyclin D2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15315760 730904 Ccnd2 cyclin D2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 730904 Ccnd2 cyclin D2 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12502747 730904 Ccnd2 cyclin D2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 730904 Ccnd2 cyclin D2 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20200402 MGI 730904 Ccnd2 cyclin D2 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15315760 730904 Ccnd2 cyclin D2 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:15315760 730904 Ccnd2 cyclin D2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:8945475 730904 Ccnd2 cyclin D2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20181227 MGI 730904 Ccnd2 cyclin D2 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20221215 MGI 730904 Ccnd2 cyclin D2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15315760 730904 Ccnd2 cyclin D2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:10101126 730904 Ccnd2 cyclin D2 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 730904 Ccnd2 cyclin D2 gene MP:0009718 absent Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:12502747 730904 Ccnd2 cyclin D2 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:12502747 730904 Ccnd2 cyclin D2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200402 MGI 730904 Ccnd2 cyclin D2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 730904 Ccnd2 cyclin D2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 730904 Ccnd2 cyclin D2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12502747 730904 Ccnd2 cyclin D2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15315760 730904 Ccnd2 cyclin D2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 730910 Slc1a7 solute carrier family 1 (glutamate transporter), member 7 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20230824 MGI PMID:34772693 730910 Slc1a7 solute carrier family 1 (glutamate transporter), member 7 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20230824 MGI PMID:34772693 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:17488640 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:21040852 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:21040852 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:21040852 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001257 increased body length IAGP N RGD:5509061 20150129 MGI PMID:25157144 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17488640 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22419158 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001260 increased body weight IAGP N RGD:5509061 20170126 MGI PMID:27693255 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001261 obese IAGP N RGD:5509061 20150129 MGI PMID:25157144 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001261 obese IAGP N RGD:5509061 20170126 MGI PMID:27693255 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23136427 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170126 MGI PMID:27693255 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:21040852 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:23136427 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22419158 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001433 polyphagia IAGP N RGD:5509061 20150129 MGI PMID:25157144 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:23136427 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:23136427 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:17122055 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17122055 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17108179 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17122055 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:17122055 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:17108179 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:21040852 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21040852 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:21040852 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20170126 MGI PMID:27693255 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17108179 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:22419158 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17122055 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17108179 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:17488640 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:17108179 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:23136427 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17108179 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17488640 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20223200 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20223200 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:17108179 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:17122055 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:24267650 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:17488640 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0004495 decreased synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:23136427 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20240418 MGI PMID:17108179 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17122055 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:17122055 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:20223200 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0005661 decreased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:17488640 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:23136427 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:23136427 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:17122055 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17488640 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:17122055 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20170126 MGI PMID:27693255 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20170126 MGI PMID:27693255 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:17122055 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:20223200 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:23136427 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20150129 MGI PMID:25157144 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0010072 increased pruritus IAGP N RGD:5509061 20141003 MGI PMID:21040852 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0010746 abnormal pre-Botzinger complex physiology IAGP N RGD:5509061 20141003 MGI PMID:17122055 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0011001 absence of AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17122055 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17488640 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17108179 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17122055 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23136427 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:17108179 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:17488640 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20160407 MGI PMID:17488640 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0014254 increased paired-pulse ratio IAGP N RGD:5509061 20230706 MGI PMID:23136427 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0014372 decreased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:17108179 730913 Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:17108179 730915 Cdx2 caudal type homeobox 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:10383162 730915 Cdx2 caudal type homeobox 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9052785 730915 Cdx2 caudal type homeobox 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19386267 730915 Cdx2 caudal type homeobox 2 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:16396910 730915 Cdx2 caudal type homeobox 2 gene MP:0000487 absent enterocytes IAGP N RGD:5509061 20141003 MGI PMID:19386267 730915 Cdx2 caudal type homeobox 2 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19386267 730915 Cdx2 caudal type homeobox 2 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22190642 730915 Cdx2 caudal type homeobox 2 gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:10383162 730915 Cdx2 caudal type homeobox 2 gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:19386267 730915 Cdx2 caudal type homeobox 2 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:10383162 730915 Cdx2 caudal type homeobox 2 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:14625550 730915 Cdx2 caudal type homeobox 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:14625550 730915 Cdx2 caudal type homeobox 2 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:22190642 730915 Cdx2 caudal type homeobox 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:9052785 730915 Cdx2 caudal type homeobox 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:19906845 730915 Cdx2 caudal type homeobox 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:9052785 730915 Cdx2 caudal type homeobox 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9052785 730915 Cdx2 caudal type homeobox 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10383162 730915 Cdx2 caudal type homeobox 2 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:19906845 730915 Cdx2 caudal type homeobox 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:16396910 730915 Cdx2 caudal type homeobox 2 gene MP:0001714 absent trophoblast giant cells IAGP N RGD:5509061 20141003 MGI PMID:15788452 730915 Cdx2 caudal type homeobox 2 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:16396910 730915 Cdx2 caudal type homeobox 2 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:16396910 730915 Cdx2 caudal type homeobox 2 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:9052785 730915 Cdx2 caudal type homeobox 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:22992952 730915 Cdx2 caudal type homeobox 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16396910 730915 Cdx2 caudal type homeobox 2 gene MP:0002043 increased colon hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10383162 730915 Cdx2 caudal type homeobox 2 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9052785 730915 Cdx2 caudal type homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19386267 730915 Cdx2 caudal type homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22814996 730915 Cdx2 caudal type homeobox 2 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9052785 730915 Cdx2 caudal type homeobox 2 gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:22190642 730915 Cdx2 caudal type homeobox 2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:10383162 730915 Cdx2 caudal type homeobox 2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16396910 730915 Cdx2 caudal type homeobox 2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9052785 730915 Cdx2 caudal type homeobox 2 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:22190642 730915 Cdx2 caudal type homeobox 2 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:19386267 730915 Cdx2 caudal type homeobox 2 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:16396910 730915 Cdx2 caudal type homeobox 2 gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:10383162 730915 Cdx2 caudal type homeobox 2 gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:14625550 730915 Cdx2 caudal type homeobox 2 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:19386267 730915 Cdx2 caudal type homeobox 2 gene MP:0003445 sirenomelia IAGP N RGD:5509061 20141003 MGI PMID:16396910 730915 Cdx2 caudal type homeobox 2 gene MP:0003445 sirenomelia IAGP N RGD:5509061 20141003 MGI PMID:19906845 730915 Cdx2 caudal type homeobox 2 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19386267 730915 Cdx2 caudal type homeobox 2 gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:19906845 730915 Cdx2 caudal type homeobox 2 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:15788452 730915 Cdx2 caudal type homeobox 2 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:14625550 730915 Cdx2 caudal type homeobox 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16396910 730915 Cdx2 caudal type homeobox 2 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:14625550 730915 Cdx2 caudal type homeobox 2 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:22190642 730915 Cdx2 caudal type homeobox 2 gene MP:0004141 abnormal enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19386267 730915 Cdx2 caudal type homeobox 2 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9052785 730915 Cdx2 caudal type homeobox 2 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16396910 730915 Cdx2 caudal type homeobox 2 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:16396910 730915 Cdx2 caudal type homeobox 2 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9052785 730915 Cdx2 caudal type homeobox 2 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:15788452 730915 Cdx2 caudal type homeobox 2 gene MP:0004963 abnormal blastocoele morphology IAGP N RGD:5509061 20141003 MGI PMID:15788452 730915 Cdx2 caudal type homeobox 2 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15788452 730915 Cdx2 caudal type homeobox 2 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15788452 730915 Cdx2 caudal type homeobox 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14625550 730915 Cdx2 caudal type homeobox 2 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14625550 730915 Cdx2 caudal type homeobox 2 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:22190642 730915 Cdx2 caudal type homeobox 2 gene MP:0008013 cecum polyps IAGP N RGD:5509061 20141003 MGI PMID:22190642 730915 Cdx2 caudal type homeobox 2 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:22190642 730915 Cdx2 caudal type homeobox 2 gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20141003 MGI PMID:19386267 730915 Cdx2 caudal type homeobox 2 gene MP:0008786 abnormal hindgut morphology IAGP N RGD:5509061 20141003 MGI PMID:19386267 730915 Cdx2 caudal type homeobox 2 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:16396910 730915 Cdx2 caudal type homeobox 2 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:19906845 730915 Cdx2 caudal type homeobox 2 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:22190642 730915 Cdx2 caudal type homeobox 2 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15788452 730915 Cdx2 caudal type homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19386267 730915 Cdx2 caudal type homeobox 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9052785 730915 Cdx2 caudal type homeobox 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15788452 730915 Cdx2 caudal type homeobox 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22992952 730915 Cdx2 caudal type homeobox 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10383162 730915 Cdx2 caudal type homeobox 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16396910 730915 Cdx2 caudal type homeobox 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19906845 730915 Cdx2 caudal type homeobox 2 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:19906845 730915 Cdx2 caudal type homeobox 2 gene MP:0011881 distended duodenum IAGP N RGD:5509061 20150702 MGI PMID:19386267 730915 Cdx2 caudal type homeobox 2 gene MP:0011884 absent colon IAGP N RGD:5509061 20150702 MGI PMID:19386267 730915 Cdx2 caudal type homeobox 2 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:10383162 730915 Cdx2 caudal type homeobox 2 gene MP:0012119 increased trophectoderm apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15788452 730915 Cdx2 caudal type homeobox 2 gene MP:0012127 absent placenta hemotrichorial membrane IAGP N RGD:5509061 20141003 MGI PMID:16396910 730915 Cdx2 caudal type homeobox 2 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:19906845 730915 Cdx2 caudal type homeobox 2 gene MP:0012182 abnormal presomitic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:19906845 730915 Cdx2 caudal type homeobox 2 gene MP:0013168 absent hindlimb buds IAGP N RGD:5509061 20141003 MGI PMID:19906845 730915 Cdx2 caudal type homeobox 2 gene MP:0013485 increased Paneth cell number IAGP N RGD:5509061 20150312 MGI PMID:22190642 730915 Cdx2 caudal type homeobox 2 gene MP:0013487 abnormal Paneth cell physiology IAGP N RGD:5509061 20150319 MGI PMID:22190642 730918 Adm adrenomedullin gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18723674 730918 Adm adrenomedullin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18723674 730918 Adm adrenomedullin gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:18723674 730918 Adm adrenomedullin gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:14620929 730918 Adm adrenomedullin gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17360661 730918 Adm adrenomedullin gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:23635772 730918 Adm adrenomedullin gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:11149956 730918 Adm adrenomedullin gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:18097475 730918 Adm adrenomedullin gene MP:0001863 blood vessel inflammation IAGP N RGD:5509061 20141003 MGI PMID:11772884 730918 Adm adrenomedullin gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:11149956 730918 Adm adrenomedullin gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:11149956 730918 Adm adrenomedullin gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:11149956 730918 Adm adrenomedullin gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11149956 730918 Adm adrenomedullin gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:11149956 730918 Adm adrenomedullin gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:16537897 730918 Adm adrenomedullin gene MP:0002450 abnormal lymph organ development IAGP N RGD:5509061 20141003 MGI PMID:18097475 730918 Adm adrenomedullin gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:18723674 730918 Adm adrenomedullin gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17360661 730918 Adm adrenomedullin gene MP:0003044 impaired basement membrane formation IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16537897 730918 Adm adrenomedullin gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0003390 lymphedema IAGP N RGD:5509061 20141003 MGI PMID:18097475 730918 Adm adrenomedullin gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:14620929 730918 Adm adrenomedullin gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:11772884 730918 Adm adrenomedullin gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11149956 730918 Adm adrenomedullin gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17360661 730918 Adm adrenomedullin gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11772884 730918 Adm adrenomedullin gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:17360661 730918 Adm adrenomedullin gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:14620929 730918 Adm adrenomedullin gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17360661 730918 Adm adrenomedullin gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:14620929 730918 Adm adrenomedullin gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14620929 730918 Adm adrenomedullin gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0008876 decreased uterine NK cell number IAGP N RGD:5509061 20141003 MGI PMID:23635772 730918 Adm adrenomedullin gene MP:0009394 increased uterine NK cell number IAGP N RGD:5509061 20141003 MGI PMID:23635772 730918 Adm adrenomedullin gene MP:0009658 increased placenta apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23635772 730918 Adm adrenomedullin gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18723674 730918 Adm adrenomedullin gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18723674 730918 Adm adrenomedullin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11149956 730918 Adm adrenomedullin gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18097475 730918 Adm adrenomedullin gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11772884 730918 Adm adrenomedullin gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:17360661 730918 Adm adrenomedullin gene MP:0011514 skin hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0011525 abnormal placenta intervillous maternal lacunae morphology IAGP N RGD:5509061 20141003 MGI PMID:23635772 730918 Adm adrenomedullin gene MP:0011526 abnormal placenta fetal blood space morphology IAGP N RGD:5509061 20141003 MGI PMID:23635772 730918 Adm adrenomedullin gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:14620929 730918 Adm adrenomedullin gene MP:0012302 umbilical artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0012303 umbilical vein stenosis IAGP N RGD:5509061 20141003 MGI PMID:11602502 730918 Adm adrenomedullin gene MP:0012727 abnormal uterine spiral artery remodeling IAGP N RGD:5509061 20141003 MGI PMID:23635772 730918 Adm adrenomedullin gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:14620929 730918 Adm adrenomedullin gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:18723674 730920 Rtn4 reticulon 4 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20230601 MGI 730920 Rtn4 reticulon 4 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20230119 MGI 730920 Rtn4 reticulon 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12718856 730920 Rtn4 reticulon 4 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 730920 Rtn4 reticulon 4 gene MP:0003407 abnormal central nervous system regeneration IAGP N RGD:5509061 20141003 MGI PMID:19587271 730920 Rtn4 reticulon 4 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12718856 730920 Rtn4 reticulon 4 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:18334965 730920 Rtn4 reticulon 4 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230119 MGI 730920 Rtn4 reticulon 4 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:12718856 730920 Rtn4 reticulon 4 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230119 MGI 730920 Rtn4 reticulon 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12718856 730920 Rtn4 reticulon 4 gene MP:0030013 enhanced central nervous system regeneration IAGP N RGD:5509061 20170713 MGI PMID:12718854 730920 Rtn4 reticulon 4 gene MP:0030013 enhanced central nervous system regeneration IAGP N RGD:5509061 20170713 MGI PMID:12718855 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:12598627 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9331345 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17362911 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9331345 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9331345 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9331345 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9331345 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9331345 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20231221 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20512151 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20512151 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:12598627 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0004062 dilated heart right atrium IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:21828096 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0008317 abnormal paravertebral ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9331345 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21828096 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:20410128 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0009798 abnormal ophthalmic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20410128 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18032673 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0010981 abnormal branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:18249526 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18249526 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18249526 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18249526 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8849723 730922 Sema3a sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:8849723 730924 E2f1 E2F transcription factor 1 gene MP:0000018 small ears IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0000040 absent middle ear ossicles IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20221103 MGI PMID:34211969 730924 E2f1 E2F transcription factor 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20210722 MGI PMID:32991838 730924 E2f1 E2F transcription factor 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20240905 MGI PMID:38630655 730924 E2f1 E2F transcription factor 1 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 730924 E2f1 E2F transcription factor 1 gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0000105 impaired ossification of basisphenoid bone IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 730924 E2f1 E2F transcription factor 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221103 MGI PMID:34211969 730924 E2f1 E2F transcription factor 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0000125 absent incisors IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:18663357 730924 E2f1 E2F transcription factor 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18663357 730924 E2f1 E2F transcription factor 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20221020 MGI PMID:25759071 730924 E2f1 E2F transcription factor 1 gene MP:0000262 poor arterial differentiation IAGP N RGD:5509061 20221020 MGI PMID:25759071 730924 E2f1 E2F transcription factor 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20210121 MGI PMID:33127760 730924 E2f1 E2F transcription factor 1 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:11511364 730924 E2f1 E2F transcription factor 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18663357 730924 E2f1 E2F transcription factor 1 gene MP:0000373 belly spot IAGP N RGD:5509061 20220721 MGI PMID:35013307 730924 E2f1 E2F transcription factor 1 gene MP:0000373 belly spot IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20240905 MGI PMID:38630655 730924 E2f1 E2F transcription factor 1 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20221013 MGI PMID:31241461 730924 E2f1 E2F transcription factor 1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0000445 short snout IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20221020 MGI PMID:25759071 730924 E2f1 E2F transcription factor 1 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20240905 MGI PMID:38630655 730924 E2f1 E2F transcription factor 1 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20210722 MGI PMID:32991838 730924 E2f1 E2F transcription factor 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20221020 MGI PMID:25759071 730924 E2f1 E2F transcription factor 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9537419 730924 E2f1 E2F transcription factor 1 gene MP:0000705 athymia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:8653790 730924 E2f1 E2F transcription factor 1 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8653790 730924 E2f1 E2F transcription factor 1 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20221103 MGI PMID:34211969 730924 E2f1 E2F transcription factor 1 gene MP:0000771 abnormal brain size IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17609112 730924 E2f1 E2F transcription factor 1 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20150326 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20150326 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0001203 increased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:15735727 730924 E2f1 E2F transcription factor 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18663357 730924 E2f1 E2F transcription factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8653790 730924 E2f1 E2F transcription factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160526 MGI PMID:25940086 730924 E2f1 E2F transcription factor 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:17608565 730924 E2f1 E2F transcription factor 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17608565 730924 E2f1 E2F transcription factor 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:11076674 730924 E2f1 E2F transcription factor 1 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210722 MGI PMID:32991838 730924 E2f1 E2F transcription factor 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0001785 edema IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9537419 730924 E2f1 E2F transcription factor 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8653790 730924 E2f1 E2F transcription factor 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8653790 730924 E2f1 E2F transcription factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9537419 730924 E2f1 E2F transcription factor 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11076674 730924 E2f1 E2F transcription factor 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20221013 MGI PMID:31241461 730924 E2f1 E2F transcription factor 1 gene MP:0002163 abnormal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18663357 730924 E2f1 E2F transcription factor 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0002251 abnormal nasopharynx morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8653790 730924 E2f1 E2F transcription factor 1 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20210121 MGI PMID:33127760 730924 E2f1 E2F transcription factor 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:9537419 730924 E2f1 E2F transcription factor 1 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:18663357 730924 E2f1 E2F transcription factor 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:11076674 730924 E2f1 E2F transcription factor 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18663357 730924 E2f1 E2F transcription factor 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11076674 730924 E2f1 E2F transcription factor 1 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0003195 calcinosis IAGP N RGD:5509061 20181122 MGI PMID:28592560 730924 E2f1 E2F transcription factor 1 gene MP:0003196 calcified skin IAGP N RGD:5509061 20181122 MGI PMID:28592560 730924 E2f1 E2F transcription factor 1 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:11909960 730924 E2f1 E2F transcription factor 1 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:8653790 730924 E2f1 E2F transcription factor 1 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0003452 abnormal parotid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0003496 increased thyroid adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9537419 730924 E2f1 E2F transcription factor 1 gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17608565 730924 E2f1 E2F transcription factor 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20221103 MGI PMID:34211969 730924 E2f1 E2F transcription factor 1 gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0003842 abnormal metopic suture morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20220217 MGI PMID:35013307 730924 E2f1 E2F transcription factor 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17608565 730924 E2f1 E2F transcription factor 1 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:11076674 730924 E2f1 E2F transcription factor 1 gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0004205 absent hyoid bone IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0004282 retrognathia IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20210121 MGI PMID:33127760 730924 E2f1 E2F transcription factor 1 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0004380 short frontal bone IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0004385 interparietal bone hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0004385 interparietal bone hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0004420 parietal bone hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0004454 absent pterygoid process IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0004455 pterygoid bone hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0004458 absent alisphenoid bone IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0004461 basisphenoid bone hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0004461 basisphenoid bone hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0004461 basisphenoid bone hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0004475 palatine bone hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20160414 MGI PMID:24741006 730924 E2f1 E2F transcription factor 1 gene MP:0004540 small maxilla IAGP N RGD:5509061 20210121 MGI PMID:33127760 730924 E2f1 E2F transcription factor 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20210121 MGI PMID:33127760 730924 E2f1 E2F transcription factor 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20221013 MGI PMID:31241461 730924 E2f1 E2F transcription factor 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20240905 MGI PMID:38630655 730924 E2f1 E2F transcription factor 1 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0004790 absent upper incisors IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0004791 absent lower incisors IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20150326 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20221013 MGI PMID:31241461 730924 E2f1 E2F transcription factor 1 gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0004898 uterine hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9537419 730924 E2f1 E2F transcription factor 1 gene MP:0004899 absent temporal bone squamous part IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0004900 absent zygomatic arch IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0004911 absent mandibular condyloid process IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0004913 absent mandibular angle IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0004915 abnormal Reichert's cartilage morphology IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:8653790 730924 E2f1 E2F transcription factor 1 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11754817 730924 E2f1 E2F transcription factor 1 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0005158 ovary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17608565 730924 E2f1 E2F transcription factor 1 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20240905 MGI PMID:38630655 730924 E2f1 E2F transcription factor 1 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11076674 730924 E2f1 E2F transcription factor 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8653790 730924 E2f1 E2F transcription factor 1 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17608565 730924 E2f1 E2F transcription factor 1 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17608565 730924 E2f1 E2F transcription factor 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:17608565 730924 E2f1 E2F transcription factor 1 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8653790 730924 E2f1 E2F transcription factor 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8653790 730924 E2f1 E2F transcription factor 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20221020 MGI PMID:25759071 730924 E2f1 E2F transcription factor 1 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20240905 MGI PMID:38630655 730924 E2f1 E2F transcription factor 1 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0008301 adrenal medulla hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9537419 730924 E2f1 E2F transcription factor 1 gene MP:0008382 gonial bone hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11909960 730924 E2f1 E2F transcription factor 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:17608565 730924 E2f1 E2F transcription factor 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15470032 730924 E2f1 E2F transcription factor 1 gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18594513 730924 E2f1 E2F transcription factor 1 gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20210121 MGI PMID:33127760 730924 E2f1 E2F transcription factor 1 gene MP:0009109 decreased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221020 MGI PMID:25759071 730924 E2f1 E2F transcription factor 1 gene MP:0009796 abnormal base-excision repair IAGP N RGD:5509061 20160414 MGI PMID:24741006 730924 E2f1 E2F transcription factor 1 gene MP:0009798 abnormal ophthalmic nerve morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0009799 abnormal maxillary nerve morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0009800 abnormal mandibular nerve morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:25759071 730924 E2f1 E2F transcription factor 1 gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20221020 MGI PMID:25759071 730924 E2f1 E2F transcription factor 1 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221013 MGI PMID:31241461 730924 E2f1 E2F transcription factor 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221020 MGI PMID:25759071 730924 E2f1 E2F transcription factor 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221013 MGI PMID:31241461 730924 E2f1 E2F transcription factor 1 gene MP:0009895 decreased palatine bone horizontal plate size IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0009897 decreased maxillary shelf size IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0009899 hyoid bone hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20221103 MGI PMID:34211969 730924 E2f1 E2F transcription factor 1 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0010287 increased reproductive system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9537419 730924 E2f1 E2F transcription factor 1 gene MP:0010326 malleus hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20210121 MGI PMID:33127760 730924 E2f1 E2F transcription factor 1 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0010458 pulmonary trunk hypoplasia IAGP N RGD:5509061 20210121 MGI PMID:33127760 730924 E2f1 E2F transcription factor 1 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20210121 MGI PMID:33127760 730924 E2f1 E2F transcription factor 1 gene MP:0010652 absent aorticopulmonary septum IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20160414 MGI PMID:24741006 730924 E2f1 E2F transcription factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20150212 MGI PMID:24662053 730924 E2f1 E2F transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221013 MGI PMID:31241461 730924 E2f1 E2F transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18663357 730924 E2f1 E2F transcription factor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20210121 MGI PMID:33127760 730924 E2f1 E2F transcription factor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9537419 730924 E2f1 E2F transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11909960 730924 E2f1 E2F transcription factor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11909960 730924 E2f1 E2F transcription factor 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0011642 abnormal bone collagen fibril morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20210121 MGI PMID:33127760 730924 E2f1 E2F transcription factor 1 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0012090 midbrain hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0012174 flat head IAGP N RGD:5509061 20240905 MGI PMID:38630655 730924 E2f1 E2F transcription factor 1 gene MP:0012176 abnormal head development IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0012178 absent frontonasal prominence IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0012264 hindbrain hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0012546 triangular face IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0012756 impaired cranial neural crest cell differentiation IAGP N RGD:5509061 20210121 MGI PMID:33127760 730924 E2f1 E2F transcription factor 1 gene MP:0012757 abnormal cranial neural crest cell migration IAGP N RGD:5509061 20210121 MGI PMID:33127760 730924 E2f1 E2F transcription factor 1 gene MP:0013208 abnormal cilium physiology IAGP N RGD:5509061 20221103 MGI PMID:34211969 730924 E2f1 E2F transcription factor 1 gene MP:0013267 first pharyngeal arch hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0013440 abnormal exorbital lacrimal gland morphology IAGP N RGD:5509061 20150326 MGI PMID:8653789 730924 E2f1 E2F transcription factor 1 gene MP:0013545 cleft hard palate IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0014012 abnormal cranial blood vasculature morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0014166 ectopic cranial bone IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0014167 ectopic bone IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0014241 abnormal intracellular organelle physiology IAGP N RGD:5509061 20240905 MGI PMID:38630655 730924 E2f1 E2F transcription factor 1 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20221013 MGI PMID:31241461 730924 E2f1 E2F transcription factor 1 gene MP:0020301 short tongue IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0020845 abnormal DNA-templated transcription IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:25759071 730924 E2f1 E2F transcription factor 1 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:31241461 730924 E2f1 E2F transcription factor 1 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0021217 abnormal palatal shelf bone ossification IAGP N RGD:5509061 20230302 MGI PMID:25759071 730924 E2f1 E2F transcription factor 1 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:15124020 730924 E2f1 E2F transcription factor 1 gene MP:0030067 narrow face IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0030084 tympanic ring hypoplasia IAGP N RGD:5509061 20241031 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0030112 zygomatic bone hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0030122 temporal bone squamous part hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0030122 temporal bone squamous part hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0030124 middle ear ossicle hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0030178 abnormal scalp morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0030250 frontonasal prominence hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0030259 mandibular condyloid process hypoplasia IAGP N RGD:5509061 20210722 MGI PMID:32991838 730924 E2f1 E2F transcription factor 1 gene MP:0030300 upper jaw to lower jaw transformation IAGP N RGD:5509061 20180201 MGI PMID:25725491 730924 E2f1 E2F transcription factor 1 gene MP:0030316 enlarged neurocranium IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0030343 maxillary prominence hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0030344 absent maxillary prominence IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0030347 mandibular prominence hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0030374 Meckel's cartilage hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 730924 E2f1 E2F transcription factor 1 gene MP:0030431 wide metopic suture IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0030431 wide metopic suture IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0030533 abnormal snout skin morphology IAGP N RGD:5509061 20181122 MGI PMID:28592560 730924 E2f1 E2F transcription factor 1 gene MP:0030533 abnormal snout skin morphology IAGP N RGD:5509061 20220929 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0030930 decreased digit pigmentation IAGP N RGD:5509061 20220721 MGI PMID:35013307 730924 E2f1 E2F transcription factor 1 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:25053435 730924 E2f1 E2F transcription factor 1 gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20240627 MGI PMID:38113115 730924 E2f1 E2F transcription factor 1 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:33996804 730924 E2f1 E2F transcription factor 1 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20221201 MGI PMID:25759071 730926 Prss8 serine protease 8 (prostasin) gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20201958 730926 Prss8 serine protease 8 (prostasin) gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:20201958 730926 Prss8 serine protease 8 (prostasin) gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:20201958 730926 Prss8 serine protease 8 (prostasin) gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:20201958 730926 Prss8 serine protease 8 (prostasin) gene MP:0000416 sparse hair IAGP N RGD:5509061 20141106 MGI PMID:24706745 730926 Prss8 serine protease 8 (prostasin) gene MP:0000416 sparse hair IAGP N RGD:5509061 20200813 MGI PMID:26719335 730926 Prss8 serine protease 8 (prostasin) gene MP:0000417 short hair IEA N RGD:5509061 20111116 MGI 730926 Prss8 serine protease 8 (prostasin) gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20201224 MGI PMID:29617460 730926 Prss8 serine protease 8 (prostasin) gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20201224 MGI PMID:29617460 730926 Prss8 serine protease 8 (prostasin) gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20201224 MGI PMID:29617460 730926 Prss8 serine protease 8 (prostasin) gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20201224 MGI PMID:29617460 730926 Prss8 serine protease 8 (prostasin) gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20201224 MGI PMID:29617460 730926 Prss8 serine protease 8 (prostasin) gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22952456 730926 Prss8 serine protease 8 (prostasin) gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:20201958 730926 Prss8 serine protease 8 (prostasin) gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141106 MGI PMID:22952456 730926 Prss8 serine protease 8 (prostasin) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20201958 730926 Prss8 serine protease 8 (prostasin) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141106 MGI PMID:24706745 730926 Prss8 serine protease 8 (prostasin) gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:20201958 730926 Prss8 serine protease 8 (prostasin) gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141106 MGI PMID:24706745 730926 Prss8 serine protease 8 (prostasin) gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20200813 MGI PMID:26719335 730926 Prss8 serine protease 8 (prostasin) gene MP:0001278 kinked vibrissae IAGP N RGD:5509061 20141106 MGI PMID:24706745 730926 Prss8 serine protease 8 (prostasin) gene MP:0001278 kinked vibrissae IAGP N RGD:5509061 20200813 MGI PMID:26719335 730926 Prss8 serine protease 8 (prostasin) gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141106 MGI PMID:24706745 730926 Prss8 serine protease 8 (prostasin) gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141106 MGI PMID:24706745 730926 Prss8 serine protease 8 (prostasin) gene MP:0001304 cataract IEA N RGD:5509061 20220519 MGI 730926 Prss8 serine protease 8 (prostasin) gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0001429 dehydration IAGP N RGD:5509061 20141106 MGI PMID:22952456 730926 Prss8 serine protease 8 (prostasin) gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:22952456 730926 Prss8 serine protease 8 (prostasin) gene MP:0001511 disheveled coat IEA N RGD:5509061 20111116 MGI 730926 Prss8 serine protease 8 (prostasin) gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:22952456 730926 Prss8 serine protease 8 (prostasin) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20201224 MGI PMID:29617460 730926 Prss8 serine protease 8 (prostasin) gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20111116 MGI 730926 Prss8 serine protease 8 (prostasin) gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20111116 MGI 730926 Prss8 serine protease 8 (prostasin) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11857812 730926 Prss8 serine protease 8 (prostasin) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180705 MGI PMID:25264521 730926 Prss8 serine protease 8 (prostasin) gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141106 MGI PMID:22952456 730926 Prss8 serine protease 8 (prostasin) gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141106 MGI PMID:24706745 730926 Prss8 serine protease 8 (prostasin) gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141106 MGI PMID:24706745 730926 Prss8 serine protease 8 (prostasin) gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:22952456 730926 Prss8 serine protease 8 (prostasin) gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:22952456 730926 Prss8 serine protease 8 (prostasin) gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20201224 MGI PMID:29617460 730926 Prss8 serine protease 8 (prostasin) gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0003809 abnormal hair shaft morphology IEA N RGD:5509061 20111116 MGI 730926 Prss8 serine protease 8 (prostasin) gene MP:0003812 abnormal hair medulla IEA N RGD:5509061 20111116 MGI 730926 Prss8 serine protease 8 (prostasin) gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:20201958 730926 Prss8 serine protease 8 (prostasin) gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20201224 MGI PMID:29617460 730926 Prss8 serine protease 8 (prostasin) gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 730926 Prss8 serine protease 8 (prostasin) gene MP:0008218 delayed emergence of vibrissae IAGP N RGD:5509061 20200813 MGI PMID:26719335 730926 Prss8 serine protease 8 (prostasin) gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141106 MGI PMID:24706745 730926 Prss8 serine protease 8 (prostasin) gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20201224 MGI PMID:29617460 730926 Prss8 serine protease 8 (prostasin) gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20201224 MGI PMID:29617460 730926 Prss8 serine protease 8 (prostasin) gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20141003 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0010179 rough coat IEA N RGD:5509061 20111116 MGI 730926 Prss8 serine protease 8 (prostasin) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:22952456 730926 Prss8 serine protease 8 (prostasin) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20201224 MGI PMID:29617460 730926 Prss8 serine protease 8 (prostasin) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141106 MGI PMID:24706745 730926 Prss8 serine protease 8 (prostasin) gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 730926 Prss8 serine protease 8 (prostasin) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 730926 Prss8 serine protease 8 (prostasin) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 730926 Prss8 serine protease 8 (prostasin) gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 730926 Prss8 serine protease 8 (prostasin) gene MP:0013589 thymus medulla hypoplasia IAGP N RGD:5509061 20150319 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0013916 decreased intestine length IAGP N RGD:5509061 20201224 MGI PMID:29617460 730926 Prss8 serine protease 8 (prostasin) gene MP:0014078 small intestinal villus atrophy IAGP N RGD:5509061 20201224 MGI PMID:29617460 730926 Prss8 serine protease 8 (prostasin) gene MP:0014222 decreased colon goblet cell number IAGP N RGD:5509061 20201224 MGI PMID:29617460 730926 Prss8 serine protease 8 (prostasin) gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220811 MGI 730926 Prss8 serine protease 8 (prostasin) gene MP:0030605 abnormal corneocyte morphology IAGP N RGD:5509061 20180628 MGI PMID:16061697 730926 Prss8 serine protease 8 (prostasin) gene MP:0031154 intestinal hemorrhage IAGP N RGD:5509061 20201224 MGI PMID:29617460 730929 Slc24a2 solute carrier family 24 (sodium/potassium/calcium exchanger), member 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16407245 730929 Slc24a2 solute carrier family 24 (sodium/potassium/calcium exchanger), member 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16407245 730929 Slc24a2 solute carrier family 24 (sodium/potassium/calcium exchanger), member 2 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:16407245 730929 Slc24a2 solute carrier family 24 (sodium/potassium/calcium exchanger), member 2 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:16407245 730929 Slc24a2 solute carrier family 24 (sodium/potassium/calcium exchanger), member 2 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16407245 730934 Bmp15 bone morphogenetic protein 15 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11376106 730934 Bmp15 bone morphogenetic protein 15 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:11376106 730934 Bmp15 bone morphogenetic protein 15 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11376106 730934 Bmp15 bone morphogenetic protein 15 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11376106 730934 Bmp15 bone morphogenetic protein 15 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11376106 730934 Bmp15 bone morphogenetic protein 15 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11376106 730934 Bmp15 bone morphogenetic protein 15 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11376106 730934 Bmp15 bone morphogenetic protein 15 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11376106 730934 Bmp15 bone morphogenetic protein 15 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:11376106 730934 Bmp15 bone morphogenetic protein 15 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:11376106 730934 Bmp15 bone morphogenetic protein 15 gene MP:0003696 abnormal zona pellucida morphology IAGP N RGD:5509061 20141003 MGI PMID:11376106 730934 Bmp15 bone morphogenetic protein 15 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:11376106 730934 Bmp15 bone morphogenetic protein 15 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:11376106 730934 Bmp15 bone morphogenetic protein 15 gene MP:0009374 absent cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:11376106 730934 Bmp15 bone morphogenetic protein 15 gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20141003 MGI PMID:11376106 730934 Bmp15 bone morphogenetic protein 15 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:11376106 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:11076688 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0000692 small spleen IEA N RGD:5509061 20111116 MGI 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:11742725 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0000743 muscle spasm IAGP N RGD:5509061 20201210 MGI PMID:28724750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17028313 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17114051 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:3429842 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0000745 tremors IAGP N RGD:5509061 20201210 MGI PMID:28724750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17114051 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20201210 MGI PMID:28724750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001391 abnormal tail movements IAGP N RGD:5509061 20201210 MGI PMID:28724750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001393 ataxia IEA N RGD:5509061 20111116 MGI 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:8062927 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001405 impaired coordination IAGP N RGD:5509061 20201210 MGI PMID:28724750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17114051 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:3429842 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:17114051 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20141003 MGI PMID:8733750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:12954867 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17114051 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:8733750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:3429842 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:12954867 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:17114051 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:3429842 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001513 limb grasping IAGP N RGD:5509061 20201210 MGI PMID:28724750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:17028313 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:17114051 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:3429842 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001523 impaired righting response IAGP N RGD:5509061 20201210 MGI PMID:28724750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001783 decreased white adipose tissue amount IEA N RGD:5509061 20111116 MGI 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:3429842 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:12954867 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20201210 MGI PMID:28724750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11742725 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0002083 premature death IAGP N RGD:5509061 20201210 MGI PMID:28724750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20201210 MGI PMID:28724750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11742725 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0002862 abnormal righting response IEA N RGD:5509061 20111116 MGI 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0002906 increased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20111116 MGI 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17114051 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20201210 MGI PMID:28724750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:17114051 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:12954867 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0003644 thymus atrophy IEA N RGD:5509061 20111116 MGI 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0003997 tonic-clonic seizures IEA N RGD:5509061 20160922 MGI 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17114051 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:17114051 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:8062927 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:11076688 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17028313 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0005551 abnormal eye electrophysiology IEA N RGD:5509061 20141003 MGI 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0005572 abnormal pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:11742725 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0005604 hyperekplexia IAGP N RGD:5509061 20141003 MGI PMID:8733750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:11742725 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20201210 MGI PMID:28724750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12954867 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17028313 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20201210 MGI PMID:28724750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0012146 increased b-wave amplitude IAGP N RGD:5509061 20141003 MGI PMID:17114051 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:28724750 730940 Glra1 glycine receptor, alpha 1 subunit gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:28724750 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:11172067 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11172067 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20220519 MGI 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11172067 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20160804 MGI 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11172067 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20201022 MGI 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160804 MGI 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11172067 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20141003 MGI PMID:11172067 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:11172067 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:11172067 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:11172067 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20141003 MGI PMID:11172067 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20160804 MGI 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0008991 abnormal bile canaliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:11172067 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20201022 MGI 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:11172067 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 730945 Abcb11 ATP-binding cassette, sub-family B member 11 gene MP:0011896 increased circulating unsaturated transferrin level IEA N RGD:5509061 20211021 MGI 730947 Crh corticotropin releasing hormone gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10686522 730947 Crh corticotropin releasing hormone gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15033910 730947 Crh corticotropin releasing hormone gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:7830793 730947 Crh corticotropin releasing hormone gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0000589 thin tail IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:7830793 730947 Crh corticotropin releasing hormone gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:7830793 730947 Crh corticotropin releasing hormone gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:9922208 730947 Crh corticotropin releasing hormone gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:7830793 730947 Crh corticotropin releasing hormone gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:9740238 730947 Crh corticotropin releasing hormone gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:9740238 730947 Crh corticotropin releasing hormone gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:15033910 730947 Crh corticotropin releasing hormone gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0001261 obese IAGP N RGD:5509061 20150129 MGI PMID:25157144 730947 Crh corticotropin releasing hormone gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22231481 730947 Crh corticotropin releasing hormone gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20170216 MGI PMID:27595593 730947 Crh corticotropin releasing hormone gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20170216 MGI PMID:27595593 730947 Crh corticotropin releasing hormone gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15843539 730947 Crh corticotropin releasing hormone gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11602623 730947 Crh corticotropin releasing hormone gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15159534 730947 Crh corticotropin releasing hormone gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:7830793 730947 Crh corticotropin releasing hormone gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 730947 Crh corticotropin releasing hormone gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:15843539 730947 Crh corticotropin releasing hormone gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15843539 730947 Crh corticotropin releasing hormone gene MP:0002664 decreased circulating adrenocorticotropin level IAGP N RGD:5509061 20170216 MGI PMID:27595593 730947 Crh corticotropin releasing hormone gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15033910 730947 Crh corticotropin releasing hormone gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20170216 MGI PMID:27595593 730947 Crh corticotropin releasing hormone gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15843539 730947 Crh corticotropin releasing hormone gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:7830793 730947 Crh corticotropin releasing hormone gene MP:0003718 maternal effect IAGP N RGD:5509061 20170216 MGI PMID:27595593 730947 Crh corticotropin releasing hormone gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:22231481 730947 Crh corticotropin releasing hormone gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0003966 abnormal adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:10686522 730947 Crh corticotropin releasing hormone gene MP:0003966 abnormal adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:11602623 730947 Crh corticotropin releasing hormone gene MP:0004781 abnormal surfactant composition IAGP N RGD:5509061 20141003 MGI PMID:9922208 730947 Crh corticotropin releasing hormone gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:15843539 730947 Crh corticotropin releasing hormone gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15843539 730947 Crh corticotropin releasing hormone gene MP:0005114 premature hair loss IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:10098506 730947 Crh corticotropin releasing hormone gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:10686522 730947 Crh corticotropin releasing hormone gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:11602623 730947 Crh corticotropin releasing hormone gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15033910 730947 Crh corticotropin releasing hormone gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15159534 730947 Crh corticotropin releasing hormone gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:7830793 730947 Crh corticotropin releasing hormone gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15159534 730947 Crh corticotropin releasing hormone gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:15033910 730947 Crh corticotropin releasing hormone gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0005568 increased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0005660 abnormal circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:15033910 730947 Crh corticotropin releasing hormone gene MP:0005661 decreased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:10686522 730947 Crh corticotropin releasing hormone gene MP:0005663 abnormal circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:15033910 730947 Crh corticotropin releasing hormone gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15033910 730947 Crh corticotropin releasing hormone gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:11602623 730947 Crh corticotropin releasing hormone gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:15843539 730947 Crh corticotropin releasing hormone gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0010809 abnormal club cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9922208 730947 Crh corticotropin releasing hormone gene MP:0010914 abnormal solitary pulmonary neuroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9922208 730947 Crh corticotropin releasing hormone gene MP:0011147 increased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:9922208 730947 Crh corticotropin releasing hormone gene MP:0011549 increased urine corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0013307 increased adrenal gland weight IAGP N RGD:5509061 20141120 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0013308 decreased adrenal gland weight IAGP N RGD:5509061 20170216 MGI PMID:27595593 730947 Crh corticotropin releasing hormone gene MP:0013366 adrenal gland atrophy IAGP N RGD:5509061 20170216 MGI PMID:27595593 730947 Crh corticotropin releasing hormone gene MP:0014286 increased adrenal gland zona fasciculata size IAGP N RGD:5509061 20230907 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0014287 decreased adrenal gland zona fasciculata size IAGP N RGD:5509061 20230907 MGI PMID:7830793 730947 Crh corticotropin releasing hormone gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:24302625 730947 Crh corticotropin releasing hormone gene MP:0030985 decreased circulating osteocalcin level IAGP N RGD:5509061 20191219 MGI PMID:24302625 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:11960699 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11960699 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000299 failure of atrioventricular cushion closure IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:11960699 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12220125 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0001169 abnormal bulbourethral gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12220125 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0001170 bulbourethral gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12220125 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:11784073 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20141003 MGI PMID:11784073 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:12838410 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0001329 retina hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11784073 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12220125 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:11784073 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:12838410 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0003094 abnormal cornea posterior stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:11784073 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0003168 abnormal scala vestibuli morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12838410 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12838410 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0003958 heart valve hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004282 retrognathia IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004283 absent cornea endothelium IAGP N RGD:5509061 20141003 MGI PMID:11784073 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004285 absent Descemet membrane IAGP N RGD:5509061 20141003 MGI PMID:11784073 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004304 absent spiral limbus IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004307 absent Rosenthal canal IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004422 small temporal bone IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004440 absent occipital bone IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004454 absent pterygoid process IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004458 absent alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004483 absent interdental cells IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004627 abnormal trochanter morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0004913 absent mandibular angle IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005198 abnormal aqueous drainage system morphology IAGP N RGD:5509061 20141003 MGI PMID:19509472 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005203 abnormal trabecular meshwork morphology IAGP N RGD:5509061 20141003 MGI PMID:19509472 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005204 abnormal canal of Schlemm morphology IAGP N RGD:5509061 20141003 MGI PMID:19509472 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005208 abnormal iris stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:11784073 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20141003 MGI PMID:19509472 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005299 abnormal eye posterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:12838410 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005299 abnormal eye posterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:11784073 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005304 bulbourethral gland cyst IAGP N RGD:5509061 20141003 MGI PMID:12220125 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005305 prostate gland anterior lobe hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12220125 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:11784073 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:12838410 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12220125 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:16257223 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11784073 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12838410 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12838410 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0006200 vitreous body deposition IAGP N RGD:5509061 20141003 MGI PMID:11784073 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:22772368 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:11960699 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:11984523 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0009085 abnormal uterine horn morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0009621 primary vitreous hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19465598 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:22772368 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0009874 abnormal interdigital cell death IAGP N RGD:5509061 20141003 MGI PMID:11960699 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010224 abnormal heart ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010419 inlet ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010419 inlet ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010433 double inlet heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010460 pulmonary artery hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010469 ascending aorta hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010469 ascending aorta hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010485 aortic arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010572 persistent right dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010605 thick pulmonary valve cusps IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010610 patent aortic valve IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010611 patent pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010620 thick mitral valve IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010629 thick tricuspid valve IAGP N RGD:5509061 20141003 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010709 absent eye anterior chamber IAGP N RGD:5509061 20201119 MGI PMID:11784073 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11784073 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0011362 ectopic adrenal gland IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0011410 ectopic testis IAGP N RGD:5509061 20141003 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:16257223 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0011575 dilated aorta bulb IAGP N RGD:5509061 20141003 MGI PMID:22772368 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:11390347 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0011781 abnormal bulbourethral gland physiology IAGP N RGD:5509061 20150416 MGI PMID:12220125 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0014234 decreased enterocyte apoptosis IAGP N RGD:5509061 20230323 MGI PMID:11984523 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0030006 decreased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:12838410 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0030258 small mandibular condyloid process IAGP N RGD:5509061 20171019 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0030283 small mandibular coronoid process IAGP N RGD:5509061 20171102 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0030388 large fontanelles IAGP N RGD:5509061 20171207 MGI PMID:9217007 730954 Tgfb2 transforming growth factor, beta 2 gene MP:0030858 small olecranon IAGP N RGD:5509061 20181025 MGI PMID:9217007 730964 Soat2 sterol O-acyltransferase 2 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11100118 730964 Soat2 sterol O-acyltransferase 2 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22460046 730964 Soat2 sterol O-acyltransferase 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:11100118 730964 Soat2 sterol O-acyltransferase 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11100118 730964 Soat2 sterol O-acyltransferase 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12538880 730964 Soat2 sterol O-acyltransferase 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22460046 730964 Soat2 sterol O-acyltransferase 2 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11100118 730964 Soat2 sterol O-acyltransferase 2 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12538880 730964 Soat2 sterol O-acyltransferase 2 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:11100118 730964 Soat2 sterol O-acyltransferase 2 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:22460046 730964 Soat2 sterol O-acyltransferase 2 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22460046 730964 Soat2 sterol O-acyltransferase 2 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22460046 730964 Soat2 sterol O-acyltransferase 2 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:11100118 730964 Soat2 sterol O-acyltransferase 2 gene MP:0005085 abnormal gallbladder physiology IAGP N RGD:5509061 20141003 MGI PMID:11100118 730964 Soat2 sterol O-acyltransferase 2 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11100118 730964 Soat2 sterol O-acyltransferase 2 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22460046 730964 Soat2 sterol O-acyltransferase 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11100118 730964 Soat2 sterol O-acyltransferase 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12538880 730964 Soat2 sterol O-acyltransferase 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22460046 730964 Soat2 sterol O-acyltransferase 2 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11100118 730964 Soat2 sterol O-acyltransferase 2 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12538880 730964 Soat2 sterol O-acyltransferase 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22460046 730964 Soat2 sterol O-acyltransferase 2 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22460046 730964 Soat2 sterol O-acyltransferase 2 gene MP:0011599 increased phosphatidylcholine-sterol O-acyltransferase activity IAGP N RGD:5509061 20141003 MGI PMID:12538880 730964 Soat2 sterol O-acyltransferase 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:11100118 730966 Pth2r parathyroid hormone 2 receptor gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20190815 MGI PMID:28890271 730966 Pth2r parathyroid hormone 2 receptor gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20190815 MGI PMID:28890271 730966 Pth2r parathyroid hormone 2 receptor gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 730966 Pth2r parathyroid hormone 2 receptor gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20190815 MGI PMID:28890271 730966 Pth2r parathyroid hormone 2 receptor gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20190815 MGI PMID:28890271 730966 Pth2r parathyroid hormone 2 receptor gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20190815 MGI PMID:28890271 730966 Pth2r parathyroid hormone 2 receptor gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20190815 MGI PMID:28890271 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15489218 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15489218 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15489218 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15489218 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:15489218 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:15489218 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15489218 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15489218 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:15489218 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:15489218 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:16223892 730968 Abcd2 ATP-binding cassette, sub-family D member 2 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15489218 730971 Dnm2 dynamin 2 gene MP:0000111 cleft palate IEA N RGD:5509061 20141003 MGI 730971 Dnm2 dynamin 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20221117 MGI PMID:28466468 730971 Dnm2 dynamin 2 gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20141003 MGI 730971 Dnm2 dynamin 2 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20141003 MGI 730971 Dnm2 dynamin 2 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20141003 MGI 730971 Dnm2 dynamin 2 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:20858595 730971 Dnm2 dynamin 2 gene MP:0000751 myopathy IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20210520 MGI 730971 Dnm2 dynamin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230504 MGI PMID:32809972 730971 Dnm2 dynamin 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20141003 MGI 730971 Dnm2 dynamin 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0001577 anemia IAGP N RGD:5509061 20221117 MGI PMID:28466468 730971 Dnm2 dynamin 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20858595 730971 Dnm2 dynamin 2 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20141003 MGI 730971 Dnm2 dynamin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20059951 730971 Dnm2 dynamin 2 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:20858595 730971 Dnm2 dynamin 2 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20221117 MGI PMID:28466468 730971 Dnm2 dynamin 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20221117 MGI PMID:28466468 730971 Dnm2 dynamin 2 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20160211 MGI PMID:25417109 730971 Dnm2 dynamin 2 gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20221117 MGI PMID:28466468 730971 Dnm2 dynamin 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20221117 MGI PMID:28466468 730971 Dnm2 dynamin 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 730971 Dnm2 dynamin 2 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20858595 730971 Dnm2 dynamin 2 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20230504 MGI PMID:32809972 730971 Dnm2 dynamin 2 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20170119 MGI PMID:27870637 730971 Dnm2 dynamin 2 gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:20858595 730971 Dnm2 dynamin 2 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:20858595 730971 Dnm2 dynamin 2 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210520 MGI 730971 Dnm2 dynamin 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20221117 MGI PMID:28466468 730971 Dnm2 dynamin 2 gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20170119 MGI PMID:27870637 730971 Dnm2 dynamin 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20059951 730971 Dnm2 dynamin 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20858595 730971 Dnm2 dynamin 2 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20160211 MGI PMID:25417109 730971 Dnm2 dynamin 2 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20141003 MGI 730971 Dnm2 dynamin 2 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20221117 MGI PMID:28466468 730971 Dnm2 dynamin 2 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:20858595 730971 Dnm2 dynamin 2 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:20858595 730971 Dnm2 dynamin 2 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20230504 MGI PMID:32809972 730971 Dnm2 dynamin 2 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:20858595 730971 Dnm2 dynamin 2 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:20858595 730971 Dnm2 dynamin 2 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:20858595 730971 Dnm2 dynamin 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 730971 Dnm2 dynamin 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20230504 MGI PMID:32809972 730971 Dnm2 dynamin 2 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20141003 MGI 730971 Dnm2 dynamin 2 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20141003 MGI 730971 Dnm2 dynamin 2 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20141003 MGI 730971 Dnm2 dynamin 2 gene MP:0010466 vascular ring IEA N RGD:5509061 20141003 MGI 730971 Dnm2 dynamin 2 gene MP:0010541 aorta hypoplasia IEA N RGD:5509061 20141003 MGI 730971 Dnm2 dynamin 2 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20858595 730971 Dnm2 dynamin 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20858595 730971 Dnm2 dynamin 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20230504 MGI PMID:32809972 730971 Dnm2 dynamin 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20059951 730971 Dnm2 dynamin 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20230504 MGI PMID:32809972 730971 Dnm2 dynamin 2 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20230504 MGI PMID:32809972 730971 Dnm2 dynamin 2 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20230504 MGI PMID:32809972 730971 Dnm2 dynamin 2 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20230504 MGI PMID:32809972 730971 Dnm2 dynamin 2 gene MP:0011730 increased myelin sheath thickness IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20230504 MGI PMID:32809972 730971 Dnm2 dynamin 2 gene MP:0012260 encephalomeningocele IEA N RGD:5509061 20141003 MGI 730971 Dnm2 dynamin 2 gene MP:0012322 decreased total tissue mass IAGP N RGD:5509061 20210304 MGI PMID:32129442 730971 Dnm2 dynamin 2 gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20221117 MGI PMID:28466468 730971 Dnm2 dynamin 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 730973 Srebf2 sterol regulatory element binding factor 2 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:21858719 730973 Srebf2 sterol regulatory element binding factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170921 MGI PMID:28244871 730973 Srebf2 sterol regulatory element binding factor 2 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:21858719 730973 Srebf2 sterol regulatory element binding factor 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20170921 MGI PMID:28244871 730973 Srebf2 sterol regulatory element binding factor 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20170921 MGI PMID:28244871 730973 Srebf2 sterol regulatory element binding factor 2 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21858719 730973 Srebf2 sterol regulatory element binding factor 2 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21858719 730973 Srebf2 sterol regulatory element binding factor 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20170921 MGI PMID:28244871 730973 Srebf2 sterol regulatory element binding factor 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20170921 MGI PMID:28244871 730973 Srebf2 sterol regulatory element binding factor 2 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21858719 730973 Srebf2 sterol regulatory element binding factor 2 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20170921 MGI PMID:28244871 730973 Srebf2 sterol regulatory element binding factor 2 gene MP:0010161 decreased brain cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21858719 730973 Srebf2 sterol regulatory element binding factor 2 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:21858719 730973 Srebf2 sterol regulatory element binding factor 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21858719 730973 Srebf2 sterol regulatory element binding factor 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21858719 730977 Cdc42 cell division cycle 42 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0000097 short maxilla IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0000111 cleft palate IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16510873 730977 Cdc42 cell division cycle 42 gene MP:0000388 absent hair follicle inner root sheath IAGP N RGD:5509061 20141003 MGI PMID:16510873 730977 Cdc42 cell division cycle 42 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20181227 MGI 730977 Cdc42 cell division cycle 42 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0000445 short snout IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23555292 730977 Cdc42 cell division cycle 42 gene MP:0000524 decreased renal tubule number IAGP N RGD:5509061 20141003 MGI PMID:23555292 730977 Cdc42 cell division cycle 42 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:23555292 730977 Cdc42 cell division cycle 42 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0000794 abnormal parietal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:22810622 730977 Cdc42 cell division cycle 42 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:17050694 730977 Cdc42 cell division cycle 42 gene MP:0000935 abnormal folding of telencephalic vesicles IAGP N RGD:5509061 20141003 MGI PMID:17050694 730977 Cdc42 cell division cycle 42 gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:17050694 730977 Cdc42 cell division cycle 42 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16510873 730977 Cdc42 cell division cycle 42 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16510873 730977 Cdc42 cell division cycle 42 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:16510873 730977 Cdc42 cell division cycle 42 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:16510873 730977 Cdc42 cell division cycle 42 gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:16510873 730977 Cdc42 cell division cycle 42 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:17050694 730977 Cdc42 cell division cycle 42 gene MP:0001314 cornea opacity IEA N RGD:5509061 20240523 MGI 730977 Cdc42 cell division cycle 42 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 730977 Cdc42 cell division cycle 42 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 730977 Cdc42 cell division cycle 42 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10898977 730977 Cdc42 cell division cycle 42 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16510873 730977 Cdc42 cell division cycle 42 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20200910 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16510873 730977 Cdc42 cell division cycle 42 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0002958 cerebral aqueductal stenosis IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 730977 Cdc42 cell division cycle 42 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20200402 MGI 730977 Cdc42 cell division cycle 42 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20160414 MGI PMID:20139097 730977 Cdc42 cell division cycle 42 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:21690310 730977 Cdc42 cell division cycle 42 gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:21690310 730977 Cdc42 cell division cycle 42 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23555292 730977 Cdc42 cell division cycle 42 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0003624 anuria IAGP N RGD:5509061 20141003 MGI PMID:23555292 730977 Cdc42 cell division cycle 42 gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:16510873 730977 Cdc42 cell division cycle 42 gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:23171661 730977 Cdc42 cell division cycle 42 gene MP:0003925 abnormal cellular glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:10898977 730977 Cdc42 cell division cycle 42 gene MP:0004041 increased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20161201 MGI PMID:25892012 730977 Cdc42 cell division cycle 42 gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:21690310 730977 Cdc42 cell division cycle 42 gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:23555292 730977 Cdc42 cell division cycle 42 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17050694 730977 Cdc42 cell division cycle 42 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:23555292 730977 Cdc42 cell division cycle 42 gene MP:0004639 fused metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20160414 MGI PMID:20139097 730977 Cdc42 cell division cycle 42 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23555292 730977 Cdc42 cell division cycle 42 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0005034 abnormal anus morphology IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:17050694 730977 Cdc42 cell division cycle 42 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 730977 Cdc42 cell division cycle 42 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20201022 MGI 730977 Cdc42 cell division cycle 42 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20181227 MGI 730977 Cdc42 cell division cycle 42 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20160414 MGI PMID:20139097 730977 Cdc42 cell division cycle 42 gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21690310 730977 Cdc42 cell division cycle 42 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20160414 MGI PMID:20139097 730977 Cdc42 cell division cycle 42 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20160414 MGI PMID:20139097 730977 Cdc42 cell division cycle 42 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0008797 facial cleft IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0008800 increased small intestinal crypt cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20160414 MGI PMID:20139097 730977 Cdc42 cell division cycle 42 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0009586 increased platelet aggregation IAGP N RGD:5509061 20160414 MGI PMID:20139097 730977 Cdc42 cell division cycle 42 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20161201 MGI PMID:25892012 730977 Cdc42 cell division cycle 42 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0009688 abnormal spinal cord central canal morphology IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0009874 abnormal interdigital cell death IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0009882 absent palatal shelf IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0009896 palatine bone horizontal plate hypoplasia IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0009898 maxillary shelf hypoplasia IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0010156 abnormal small intestinal crypt cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:21690310 730977 Cdc42 cell division cycle 42 gene MP:0010686 abnormal hair follicle matrix region morphology IAGP N RGD:5509061 20141003 MGI PMID:16510873 730977 Cdc42 cell division cycle 42 gene MP:0010802 abnormal intestinal enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0011057 absent brain ependyma motile cilia IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23555292 730977 Cdc42 cell division cycle 42 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20220922 MGI PMID:28326341 730977 Cdc42 cell division cycle 42 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10898977 730977 Cdc42 cell division cycle 42 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11431694 730977 Cdc42 cell division cycle 42 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17050694 730977 Cdc42 cell division cycle 42 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 730977 Cdc42 cell division cycle 42 gene MP:0011184 absent embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:10898977 730977 Cdc42 cell division cycle 42 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:23555292 730977 Cdc42 cell division cycle 42 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:21690310 730977 Cdc42 cell division cycle 42 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 730977 Cdc42 cell division cycle 42 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 730977 Cdc42 cell division cycle 42 gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20160310 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0014076 absent Paneth cells IAGP N RGD:5509061 20160310 MGI PMID:22354172 730977 Cdc42 cell division cycle 42 gene MP:0014561 decreased cortical ventricular zone cell density IAGP N RGD:5509061 20241031 MGI PMID:23150167 730977 Cdc42 cell division cycle 42 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20230615 MGI PMID:10898977 730977 Cdc42 cell division cycle 42 gene MP:0030393 delayed fontanelle closure IAGP N RGD:5509061 20171214 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0030806 abnormal autopod joint morphology IAGP N RGD:5509061 20181025 MGI PMID:22387309 730977 Cdc42 cell division cycle 42 gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:20139097 730977 Cdc42 cell division cycle 42 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:22387309 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:12059962 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20160211 MGI PMID:19615374 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:12059962 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:15504734 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12059962 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12059962 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12059962 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:12059962 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12059962 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002083 premature death IAGP N RGD:5509061 20160211 MGI PMID:19615374 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12059962 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16522634 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:16522634 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:12059962 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20160211 MGI PMID:19615374 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20160211 MGI PMID:19615374 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17046694 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:17046694 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20160211 MGI PMID:19615374 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:16522634 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12059962 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20160211 MGI PMID:19615374 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0006300 abnormal entorhinal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16522634 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12059962 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:12059962 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0009974 decreased cerebral cortex pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20160211 MGI PMID:19615374 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0011445 abnormal renal protein reabsorption IAGP N RGD:5509061 20141003 MGI PMID:20351103 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20160211 MGI PMID:19615374 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0030003 hippocampus atrophy IAGP N RGD:5509061 20170706 MGI PMID:12059962 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:11182090 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:12470859 730987 Clcn3 chloride channel, voltage-sensitive 3 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:19615374 730991 Efna1 ephrin A1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20160804 MGI 730991 Efna1 ephrin A1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:20960543 730991 Efna1 ephrin A1 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20160922 MGI PMID:24652767 730991 Efna1 ephrin A1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20960543 730991 Efna1 ephrin A1 gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20160922 MGI PMID:24652767 730991 Efna1 ephrin A1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20960543 730991 Efna1 ephrin A1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:20960543 730991 Efna1 ephrin A1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:20960543 730991 Efna1 ephrin A1 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:20960543 730991 Efna1 ephrin A1 gene MP:0010101 increased sacral vertebrae number IAGP N RGD:5509061 20160922 MGI PMID:24652767 730991 Efna1 ephrin A1 gene MP:0010344 increased hibernoma incidence IAGP N RGD:5509061 20160922 MGI PMID:24652767 730991 Efna1 ephrin A1 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20141003 MGI PMID:20960543 730991 Efna1 ephrin A1 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20141003 MGI PMID:20960543 730991 Efna1 ephrin A1 gene MP:0010617 thick mitral valve cusps IAGP N RGD:5509061 20141003 MGI PMID:20960543 730991 Efna1 ephrin A1 gene MP:0010620 thick mitral valve IAGP N RGD:5509061 20141003 MGI PMID:20960543 730991 Efna1 ephrin A1 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:20960543 730994 Gnai2 G protein subunit alpha i2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:23236180 730994 Gnai2 G protein subunit alpha i2 gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17289675 730994 Gnai2 G protein subunit alpha i2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17360531 730994 Gnai2 G protein subunit alpha i2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17360531 730994 Gnai2 G protein subunit alpha i2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:7663509 730994 Gnai2 G protein subunit alpha i2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20150219 MGI PMID:24899231 730994 Gnai2 G protein subunit alpha i2 gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:7663509 730994 Gnai2 G protein subunit alpha i2 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:7663509 730994 Gnai2 G protein subunit alpha i2 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16456099 730994 Gnai2 G protein subunit alpha i2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7663509 730994 Gnai2 G protein subunit alpha i2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0001665 chronic diarrhea IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7663509 730994 Gnai2 G protein subunit alpha i2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16456099 730994 Gnai2 G protein subunit alpha i2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7663509 730994 Gnai2 G protein subunit alpha i2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150219 MGI PMID:24899231 730994 Gnai2 G protein subunit alpha i2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17289675 730994 Gnai2 G protein subunit alpha i2 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17242370 730994 Gnai2 G protein subunit alpha i2 gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17360531 730994 Gnai2 G protein subunit alpha i2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:7663509 730994 Gnai2 G protein subunit alpha i2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:7663509 730994 Gnai2 G protein subunit alpha i2 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16456099 730994 Gnai2 G protein subunit alpha i2 gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:15219458 730994 Gnai2 G protein subunit alpha i2 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:7663509 730994 Gnai2 G protein subunit alpha i2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0002899 fatigue IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7663509 730994 Gnai2 G protein subunit alpha i2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15219458 730994 Gnai2 G protein subunit alpha i2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:7663509 730994 Gnai2 G protein subunit alpha i2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20150219 MGI PMID:24899231 730994 Gnai2 G protein subunit alpha i2 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:17360531 730994 Gnai2 G protein subunit alpha i2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22550081 730994 Gnai2 G protein subunit alpha i2 gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:23236180 730994 Gnai2 G protein subunit alpha i2 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17360531 730994 Gnai2 G protein subunit alpha i2 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17360531 730994 Gnai2 G protein subunit alpha i2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17360531 730994 Gnai2 G protein subunit alpha i2 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17242370 730994 Gnai2 G protein subunit alpha i2 gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16456099 730994 Gnai2 G protein subunit alpha i2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:23236180 730994 Gnai2 G protein subunit alpha i2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:22550081 730994 Gnai2 G protein subunit alpha i2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15219458 730994 Gnai2 G protein subunit alpha i2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:17242370 730994 Gnai2 G protein subunit alpha i2 gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:17242370 730994 Gnai2 G protein subunit alpha i2 gene MP:0008626 increased circulating interleukin-5 level IAGP N RGD:5509061 20141003 MGI PMID:17242370 730994 Gnai2 G protein subunit alpha i2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:15219458 730994 Gnai2 G protein subunit alpha i2 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:17242370 730994 Gnai2 G protein subunit alpha i2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16456099 730994 Gnai2 G protein subunit alpha i2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:8613481 730994 Gnai2 G protein subunit alpha i2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16456099 730994 Gnai2 G protein subunit alpha i2 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:17360531 730994 Gnai2 G protein subunit alpha i2 gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:22550081 730994 Gnai2 G protein subunit alpha i2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7663509 730994 Gnai2 G protein subunit alpha i2 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14612574 730994 Gnai2 G protein subunit alpha i2 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7663509 730996 Hsf1 heat shock factor 1 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:12112007 730996 Hsf1 heat shock factor 1 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18485534 730996 Hsf1 heat shock factor 1 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:18485534 730996 Hsf1 heat shock factor 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:15183515 730996 Hsf1 heat shock factor 1 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15183515 730996 Hsf1 heat shock factor 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:15183515 730996 Hsf1 heat shock factor 1 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:15183515 730996 Hsf1 heat shock factor 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18485534 730996 Hsf1 heat shock factor 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:14994269 730996 Hsf1 heat shock factor 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:14994269 730996 Hsf1 heat shock factor 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12954729 730996 Hsf1 heat shock factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10545106 730996 Hsf1 heat shock factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14994269 730996 Hsf1 heat shock factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14994269 730996 Hsf1 heat shock factor 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:15483628 730996 Hsf1 heat shock factor 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 730996 Hsf1 heat shock factor 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 730996 Hsf1 heat shock factor 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10545106 730996 Hsf1 heat shock factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10545106 730996 Hsf1 heat shock factor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14994269 730996 Hsf1 heat shock factor 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10545106 730996 Hsf1 heat shock factor 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11048707 730996 Hsf1 heat shock factor 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:12112007 730996 Hsf1 heat shock factor 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14994269 730996 Hsf1 heat shock factor 1 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:14994269 730996 Hsf1 heat shock factor 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:18485534 730996 Hsf1 heat shock factor 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10545106 730996 Hsf1 heat shock factor 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15183515 730996 Hsf1 heat shock factor 1 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:14994269 730996 Hsf1 heat shock factor 1 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15183515 730996 Hsf1 heat shock factor 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12954729 730996 Hsf1 heat shock factor 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:14994269 730996 Hsf1 heat shock factor 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:18485534 730996 Hsf1 heat shock factor 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10545106 730996 Hsf1 heat shock factor 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18485534 730996 Hsf1 heat shock factor 1 gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:11048707 730996 Hsf1 heat shock factor 1 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:15183515 730996 Hsf1 heat shock factor 1 gene MP:0004079 abnormal putamen morphology IAGP N RGD:5509061 20141003 MGI PMID:15183515 730996 Hsf1 heat shock factor 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12954729 730996 Hsf1 heat shock factor 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:14994269 730996 Hsf1 heat shock factor 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:21690297 730996 Hsf1 heat shock factor 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:18485534 730996 Hsf1 heat shock factor 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 730996 Hsf1 heat shock factor 1 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:15183515 730996 Hsf1 heat shock factor 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:14994269 730996 Hsf1 heat shock factor 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:10545106 730996 Hsf1 heat shock factor 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18485534 730996 Hsf1 heat shock factor 1 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:18485534 730996 Hsf1 heat shock factor 1 gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20141003 MGI PMID:15483628 730996 Hsf1 heat shock factor 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:12112007 730996 Hsf1 heat shock factor 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20141003 MGI PMID:21690297 730996 Hsf1 heat shock factor 1 gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20141003 MGI PMID:21690297 730996 Hsf1 heat shock factor 1 gene MP:0009769 abnormal meiotic spindle assembly checkpoint IAGP N RGD:5509061 20141003 MGI PMID:21690297 730996 Hsf1 heat shock factor 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10545106 730996 Hsf1 heat shock factor 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14994269 730996 Hsf1 heat shock factor 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9516453 730996 Hsf1 heat shock factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 730996 Hsf1 heat shock factor 1 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20160421 MGI 730996 Hsf1 heat shock factor 1 gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:10545106 730996 Hsf1 heat shock factor 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:14994269 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20220811 MGI 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160922 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20160922 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20180927 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180927 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0005202 lethargy IAGP N RGD:5509061 20180927 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20160922 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20160922 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180927 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20160922 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0008831 abnormal insulin-like growth factor I level IAGP N RGD:5509061 20180927 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160922 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220519 MGI 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0011467 decreased urine urea nitrogen level IAGP N RGD:5509061 20180927 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0011652 increased circulating histidine level IAGP N RGD:5509061 20160922 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0011736 decreased urine ammonia level IAGP N RGD:5509061 20160922 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20160922 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0013724 decreased circulating tyrosine level IAGP N RGD:5509061 20160922 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0030625 increased circulating cysteine level IAGP N RGD:5509061 20180927 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0030674 decreased circulating alanine level IAGP N RGD:5509061 20180927 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0030698 decreased phenylalanine level IAGP N RGD:5509061 20180927 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0030703 increased circulating threonine level IAGP N RGD:5509061 20180927 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0030706 increased glutamine level IAGP N RGD:5509061 20180927 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0030707 decreased glutamine level IAGP N RGD:5509061 20180927 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0030733 decreased gamma-aminobutyric acid level IAGP N RGD:5509061 20180927 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0030737 decreased glutamic acid level IAGP N RGD:5509061 20180927 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0030748 decreased leucine level IAGP N RGD:5509061 20180927 MGI PMID:26490457 730998 Slc38a3 solute carrier family 38, member 3 gene MP:0030750 increased circulating leucine level IAGP N RGD:5509061 20180927 MGI PMID:26490457 731001 Il10ra interleukin 10 receptor, alpha gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20181227 MGI 731001 Il10ra interleukin 10 receptor, alpha gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22711892 731001 Il10ra interleukin 10 receptor, alpha gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20211021 MGI 731001 Il10ra interleukin 10 receptor, alpha gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:22711892 731001 Il10ra interleukin 10 receptor, alpha gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16160826 731001 Il10ra interleukin 10 receptor, alpha gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:19188497 731001 Il10ra interleukin 10 receptor, alpha gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 731001 Il10ra interleukin 10 receptor, alpha gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:16160826 731001 Il10ra interleukin 10 receptor, alpha gene MP:0004972 abnormal regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22711892 731001 Il10ra interleukin 10 receptor, alpha gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 731001 Il10ra interleukin 10 receptor, alpha gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22711892 731001 Il10ra interleukin 10 receptor, alpha gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:19941312 731001 Il10ra interleukin 10 receptor, alpha gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 731001 Il10ra interleukin 10 receptor, alpha gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 731001 Il10ra interleukin 10 receptor, alpha gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:19941312 731001 Il10ra interleukin 10 receptor, alpha gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19941312 731001 Il10ra interleukin 10 receptor, alpha gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:19941312 731001 Il10ra interleukin 10 receptor, alpha gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:19941312 731001 Il10ra interleukin 10 receptor, alpha gene MP:0008599 increased circulating interleukin-2 level IAGP N RGD:5509061 20141003 MGI PMID:19941312 731001 Il10ra interleukin 10 receptor, alpha gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:19941312 731001 Il10ra interleukin 10 receptor, alpha gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:19941312 731001 Il10ra interleukin 10 receptor, alpha gene MP:0008638 increased circulating interleukin-1 alpha level IAGP N RGD:5509061 20141003 MGI PMID:19941312 731001 Il10ra interleukin 10 receptor, alpha gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:19941312 731001 Il10ra interleukin 10 receptor, alpha gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:19941312 731001 Il10ra interleukin 10 receptor, alpha gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:19941312 731001 Il10ra interleukin 10 receptor, alpha gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22711892 731001 Il10ra interleukin 10 receptor, alpha gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20141003 MGI PMID:19941312 731004 Gnai3 G protein subunit alpha i3 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:23236180 731004 Gnai3 G protein subunit alpha i3 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:23236180 731004 Gnai3 G protein subunit alpha i3 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17289675 731004 Gnai3 G protein subunit alpha i3 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:23236180 731004 Gnai3 G protein subunit alpha i3 gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:23236180 731004 Gnai3 G protein subunit alpha i3 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:23236180 731004 Gnai3 G protein subunit alpha i3 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:23236180 731004 Gnai3 G protein subunit alpha i3 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15788486 731004 Gnai3 G protein subunit alpha i3 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:15788486 731004 Gnai3 G protein subunit alpha i3 gene MP:0009818 abnormal thromboxane level IAGP N RGD:5509061 20141003 MGI PMID:15788486 731004 Gnai3 G protein subunit alpha i3 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:23236180 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:10683376 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12428686 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10683376 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:9346237 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17219415 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:8945508 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:10683376 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16732282 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19357295 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:17110378 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11158594 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10683376 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11444591 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10683376 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19376970 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001422 abnormal drinking behavior IAGP N RGD:5509061 20141003 MGI PMID:12183660 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11158594 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10683376 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:9346237 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10342859 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:10342859 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:17110378 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:19357295 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:16732282 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17110378 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10342859 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10954756 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17110378 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11158594 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:16556900 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:20061361 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10987272 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15480979 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11444591 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17110378 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12428686 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10987272 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17219415 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17202128 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:10954756 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:17110378 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16496341 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17110378 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:17114452 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:16614756 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:14630706 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:10342859 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19357295 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002735 abnormal chemical nociception IAGP N RGD:5509061 20141003 MGI PMID:19127021 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:16556900 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:19127021 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:19376970 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19959875 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:18355636 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18355636 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:12428686 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:16732282 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20141003 MGI PMID:12054171 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:17110378 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003075 abnormal response to CNS ischemic injury IAGP N RGD:5509061 20141003 MGI PMID:11158633 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:10944235 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:11158594 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16732282 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003177 allodynia IAGP N RGD:5509061 20141003 MGI PMID:16556900 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12428686 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:8945508 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003299 gastric polyps IAGP N RGD:5509061 20141003 MGI PMID:15480979 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:10683376 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:17110378 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003357 impaired granulosa cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10342859 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003422 abnormal thrombolysis IAGP N RGD:5509061 20141003 MGI PMID:16614756 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003426 pulmonary interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11290559 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:16556900 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003626 kidney medulla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:12183660 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20141003 MGI PMID:10216176 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20141003 MGI PMID:19758985 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:9346237 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:12428686 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:18355636 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004155 decreased susceptibility to induced pancreatitis IAGP N RGD:5509061 20141003 MGI PMID:12381531 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:11705824 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:20061361 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004504 decreased incidence of tumors by UV induction IAGP N RGD:5509061 20141003 MGI PMID:17219415 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:19357295 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:19376970 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:17114452 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004867 decreased platelet calcium level IAGP N RGD:5509061 20141003 MGI PMID:10727451 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:10342859 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:12428686 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:16732282 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:12118094 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17114452 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17330822 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:16688111 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:15084473 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:12381531 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16732282 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19357295 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:12381531 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12428686 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16732282 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17110378 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:19357295 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:19376970 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:16614756 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:12428686 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:12428686 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17110378 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:19357295 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005571 decreased lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:12381531 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:10954756 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:11444591 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:11444591 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11444591 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:11158633 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19959875 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16614756 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19959875 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0006238 abnormal choriocapillaris morphology IAGP N RGD:5509061 20191212 MGI PMID:18288886 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008004 abnormal stomach pH IAGP N RGD:5509061 20141003 MGI PMID:15542509 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:10987272 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:15480979 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008095 abnormal memory B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17114452 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:18355636 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11158633 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12054171 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:10727451 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:17114452 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:17114452 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:17114452 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:10954756 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:10683376 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20061361 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:12381531 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:11832369 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:19758985 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:11158594 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15542509 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11444591 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:19376970 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009148 pancreas necrosis IAGP N RGD:5509061 20141003 MGI PMID:12381531 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009373 abnormal cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:10342859 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009586 increased platelet aggregation IAGP N RGD:5509061 20200917 MGI PMID:19357295 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19357295 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:16688111 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10683376 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18355636 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20061361 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:11444591 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:10342859 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:10683376 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:10727451 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:10987272 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:11158633 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:11444591 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:14630706 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:16688111 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:16732282 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:17219415 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:18355636 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0010985 abnormal kidney mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:12428686 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0010985 abnormal kidney mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11158594 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11158594 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10944235 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16732282 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11158594 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17110378 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12428686 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20170413 MGI PMID:19758985 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011308 kidney corticomedullary cyst IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011352 proximal convoluted tubule brush border loss IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011376 abnormal kidney corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011383 abnormal kidney capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011403 pyelonephritis IAGP N RGD:5509061 20141003 MGI PMID:7477380 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011408 renal tubule hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20141003 MGI PMID:16732282 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20141003 MGI PMID:8521477 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011534 granular kidney IAGP N RGD:5509061 20141003 MGI PMID:12428686 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011563 increased urine prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:19758985 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011564 decreased urine prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:16614756 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011564 decreased urine prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:17110378 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:11115063 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:12428686 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0012008 delayed parturition IAGP N RGD:5509061 20141003 MGI PMID:11158594 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:19376970 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0012737 abnormal primary polar body morphology IAGP N RGD:5509061 20141003 MGI PMID:9346237 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:15084473 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:16614756 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:19357295 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:11319164 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:9346237 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:10342859 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220804 MGI PMID:10342859 731007 Ptgs2 prostaglandin-endoperoxide synthase 2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:19376970 731009 Tacr1 tachykinin receptor 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:11172050 731009 Tacr1 tachykinin receptor 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:9748515 731009 Tacr1 tachykinin receptor 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9748515 731009 Tacr1 tachykinin receptor 1 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11172050 731009 Tacr1 tachykinin receptor 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:8781237 731009 Tacr1 tachykinin receptor 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9537323 731009 Tacr1 tachykinin receptor 1 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:9748515 731009 Tacr1 tachykinin receptor 1 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:15208590 731009 Tacr1 tachykinin receptor 1 gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:9537323 731009 Tacr1 tachykinin receptor 1 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:11433347 731009 Tacr1 tachykinin receptor 1 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:9537323 731009 Tacr1 tachykinin receptor 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11465604 731009 Tacr1 tachykinin receptor 1 gene MP:0002281 abnormal respiratory mucosa goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15208590 731009 Tacr1 tachykinin receptor 1 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12867261 731009 Tacr1 tachykinin receptor 1 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:11172050 731009 Tacr1 tachykinin receptor 1 gene MP:0002735 abnormal chemical nociception IAGP N RGD:5509061 20141003 MGI PMID:9537323 731009 Tacr1 tachykinin receptor 1 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:10718319 731009 Tacr1 tachykinin receptor 1 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:14625445 731009 Tacr1 tachykinin receptor 1 gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:12867261 731009 Tacr1 tachykinin receptor 1 gene MP:0003481 decreased nerve fiber response intensity IAGP N RGD:5509061 20141003 MGI PMID:9537323 731009 Tacr1 tachykinin receptor 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:10954331 731009 Tacr1 tachykinin receptor 1 gene MP:0003663 abnormal thermosensation IAGP N RGD:5509061 20141003 MGI PMID:15964684 731009 Tacr1 tachykinin receptor 1 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:9748515 731009 Tacr1 tachykinin receptor 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:11172050 731009 Tacr1 tachykinin receptor 1 gene MP:0005407 hyperalgesia IAGP N RGD:5509061 20141003 MGI PMID:14625445 731009 Tacr1 tachykinin receptor 1 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:10718319 731009 Tacr1 tachykinin receptor 1 gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:9537323 731009 Tacr1 tachykinin receptor 1 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:10718319 731009 Tacr1 tachykinin receptor 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11172050 731009 Tacr1 tachykinin receptor 1 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:9748515 731009 Tacr1 tachykinin receptor 1 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11172050 731009 Tacr1 tachykinin receptor 1 gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:9748515 731009 Tacr1 tachykinin receptor 1 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20141003 MGI PMID:9748515 731009 Tacr1 tachykinin receptor 1 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:11172050 731009 Tacr1 tachykinin receptor 1 gene MP:0020844 abnormal pulmonary respiratory rate response IAGP N RGD:5509061 20181101 MGI PMID:12492418 731009 Tacr1 tachykinin receptor 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:15814105 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20150416 MGI PMID:25294941 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20150416 MGI PMID:25294941 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0001181 absent lungs IAGP N RGD:5509061 20150416 MGI PMID:25294941 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20150416 MGI PMID:25294941 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0001785 edema IAGP N RGD:5509061 20150416 MGI PMID:25294941 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160421 MGI PMID:26832406 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20150416 MGI PMID:25294941 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0003641 small lung IAGP N RGD:5509061 20150416 MGI PMID:25294941 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20150416 MGI PMID:25294941 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20160414 MGI PMID:26832406 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0005262 coloboma IAGP N RGD:5509061 20150416 MGI PMID:25294941 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20201022 MGI 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20150416 MGI PMID:25294941 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20160414 MGI PMID:26832406 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20160414 MGI PMID:26832406 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20160414 MGI PMID:26832406 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20160414 MGI PMID:26832406 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20150416 MGI PMID:25294941 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0011998 decreased embryonic cilium length IAGP N RGD:5509061 20150416 MGI PMID:25294941 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20150416 MGI PMID:25294941 731011 Dynll1 dynein light chain LC8-type 1 gene MP:0013213 abnormal embryonic neuroepithelium primary cilium morphology IAGP N RGD:5509061 20150416 MGI PMID:25294941 731014 Ccn2 cellular communication network factor 2 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20534727 731014 Ccn2 cellular communication network factor 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0000101 absent ethmoid bone IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20534727 731014 Ccn2 cellular communication network factor 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19131512 731014 Ccn2 cellular communication network factor 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:19131512 731014 Ccn2 cellular communication network factor 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19131512 731014 Ccn2 cellular communication network factor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:18213577 731014 Ccn2 cellular communication network factor 2 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18213577 731014 Ccn2 cellular communication network factor 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:19131512 731014 Ccn2 cellular communication network factor 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 731014 Ccn2 cellular communication network factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160218 MGI PMID:26727548 731014 Ccn2 cellular communication network factor 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:18213577 731014 Ccn2 cellular communication network factor 2 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18213577 731014 Ccn2 cellular communication network factor 2 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:19131512 731014 Ccn2 cellular communication network factor 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20170601 MGI PMID:26699479 731014 Ccn2 cellular communication network factor 2 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20170601 MGI PMID:26699479 731014 Ccn2 cellular communication network factor 2 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:18213577 731014 Ccn2 cellular communication network factor 2 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0004372 bowed fibula IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0004391 abnormal respiratory conducting tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18213577 731014 Ccn2 cellular communication network factor 2 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:20936632 731014 Ccn2 cellular communication network factor 2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:18213577 731014 Ccn2 cellular communication network factor 2 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19131512 731014 Ccn2 cellular communication network factor 2 gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0008798 lateral facial cleft IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20936632 731014 Ccn2 cellular communication network factor 2 gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0010395 abnormal pharyngeal arch development IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0010827 small lung saccule IAGP N RGD:5509061 20141003 MGI PMID:18213577 731014 Ccn2 cellular communication network factor 2 gene MP:0010889 small alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:18213577 731014 Ccn2 cellular communication network factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19131512 731014 Ccn2 cellular communication network factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0011148 decreased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:18213577 731014 Ccn2 cellular communication network factor 2 gene MP:0012236 abnormal cholangiocyte morphology IAGP N RGD:5509061 20170601 MGI PMID:26699479 731014 Ccn2 cellular communication network factor 2 gene MP:0012514 pectus excavatum IAGP N RGD:5509061 20141003 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:12736220 731014 Ccn2 cellular communication network factor 2 gene MP:0030066 short face IAGP N RGD:5509061 20170921 MGI PMID:20877562 731014 Ccn2 cellular communication network factor 2 gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:12736220 731017 Pla2g2a phospholipase A2, group IIA (platelets, synovial fluid) gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:12750251 731017 Pla2g2a phospholipase A2, group IIA (platelets, synovial fluid) gene MP:0012424 decreased alimentary system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8242739 731017 Pla2g2a phospholipase A2, group IIA (platelets, synovial fluid) gene MP:0012434 decreased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8242739 731020 Adora2b adenosine A2b receptor gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:17353435 731020 Adora2b adenosine A2b receptor gene MP:0000947 convulsive seizures IEA N RGD:5509061 20201231 MGI 731020 Adora2b adenosine A2b receptor gene MP:0001379 abnormal penile erection IAGP N RGD:5509061 20141003 MGI PMID:18340377 731020 Adora2b adenosine A2b receptor gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20170601 MGI PMID:25538227 731020 Adora2b adenosine A2b receptor gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16823489 731020 Adora2b adenosine A2b receptor gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18559975 731020 Adora2b adenosine A2b receptor gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:21242513 731020 Adora2b adenosine A2b receptor gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:21242513 731020 Adora2b adenosine A2b receptor gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 731020 Adora2b adenosine A2b receptor gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:18056839 731020 Adora2b adenosine A2b receptor gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:16823489 731020 Adora2b adenosine A2b receptor gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:16823489 731020 Adora2b adenosine A2b receptor gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21242513 731020 Adora2b adenosine A2b receptor gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:18056839 731020 Adora2b adenosine A2b receptor gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20180503 MGI PMID:23603835 731020 Adora2b adenosine A2b receptor gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:21242513 731020 Adora2b adenosine A2b receptor gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20170601 MGI PMID:25538227 731020 Adora2b adenosine A2b receptor gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 731020 Adora2b adenosine A2b receptor gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:17200408 731020 Adora2b adenosine A2b receptor gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21242513 731020 Adora2b adenosine A2b receptor gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21242513 731020 Adora2b adenosine A2b receptor gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:16823489 731020 Adora2b adenosine A2b receptor gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:16823489 731020 Adora2b adenosine A2b receptor gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:17525287 731020 Adora2b adenosine A2b receptor gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17200408 731020 Adora2b adenosine A2b receptor gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21242513 731020 Adora2b adenosine A2b receptor gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:16823489 731020 Adora2b adenosine A2b receptor gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:16823489 731020 Adora2b adenosine A2b receptor gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16823489 731020 Adora2b adenosine A2b receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17200408 731020 Adora2b adenosine A2b receptor gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17200408 731020 Adora2b adenosine A2b receptor gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21242513 731020 Adora2b adenosine A2b receptor gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:17200408 731020 Adora2b adenosine A2b receptor gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 731020 Adora2b adenosine A2b receptor gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:17200408 731020 Adora2b adenosine A2b receptor gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 731020 Adora2b adenosine A2b receptor gene MP:0020333 enhanced leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:16823489 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11344090 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:11211878 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21302256 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15308581 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10967099 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:11211878 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:10967099 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:11211878 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:12754417 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11211878 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:11211878 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:11344090 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10967099 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:10967099 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11344090 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11861419 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12767889 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21302256 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:10967099 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:11344090 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:10967099 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10967099 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11344090 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:11344090 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:12754417 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:10967099 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:11344090 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:21302256 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11211878 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12754417 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21302256 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21559415 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21659499 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15308581 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11874986 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:21659499 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:21302256 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:21659499 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:11211878 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10967099 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10967099 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11344090 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:12754417 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:12754417 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:21302256 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:11874986 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0003820 increased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:11874986 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:11211878 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11344090 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12754417 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:10967099 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:12754417 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:11874986 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:10967099 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:11344090 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:21302256 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0004092 absent Z line IAGP N RGD:5509061 20141003 MGI PMID:12781968 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:15308581 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15308581 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12754417 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11211878 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12754417 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11874986 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0006343 enlarged first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:21302256 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:15308581 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10967099 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12767889 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:21659499 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0010148 abnormal exocrine pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:21659499 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21659499 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10967099 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11211878 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11344090 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11861419 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12754417 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21302256 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20141003 MGI PMID:12781968 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20141003 MGI PMID:12781968 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:12781968 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0011637 abnormal mitochondrial matrix morphology IAGP N RGD:5509061 20141003 MGI PMID:12781968 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20150611 MGI PMID:21659499 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0012127 absent placenta hemotrichorial membrane IAGP N RGD:5509061 20141003 MGI PMID:21302256 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:11211878 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:11344090 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0031607 abnormal fetal cardiomyocyte mitochondrial morphology IAGP N RGD:5509061 20240509 MGI PMID:12781968 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0031611 decreased fetal cardiomyocyte number IAGP N RGD:5509061 20240509 MGI PMID:10967099 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0031613 fetal cardiomyocyte disarray IAGP N RGD:5509061 20240509 MGI PMID:11344090 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0031613 fetal cardiomyocyte disarray IAGP N RGD:5509061 20240509 MGI PMID:12781968 731022 Slc8a1 solute carrier family 8 (sodium/calcium exchanger), member 1 gene MP:0031635 increased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:11874986 731024 Pcsk9 proprotein convertase subtilisin/kexin type 9 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18666258 731024 Pcsk9 proprotein convertase subtilisin/kexin type 9 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15805190 731024 Pcsk9 proprotein convertase subtilisin/kexin type 9 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18666258 731024 Pcsk9 proprotein convertase subtilisin/kexin type 9 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23614904 731024 Pcsk9 proprotein convertase subtilisin/kexin type 9 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15805190 731024 Pcsk9 proprotein convertase subtilisin/kexin type 9 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18666258 731024 Pcsk9 proprotein convertase subtilisin/kexin type 9 gene MP:0002658 abnormal liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:18666258 731024 Pcsk9 proprotein convertase subtilisin/kexin type 9 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 731024 Pcsk9 proprotein convertase subtilisin/kexin type 9 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:23614904 731024 Pcsk9 proprotein convertase subtilisin/kexin type 9 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15805190 731024 Pcsk9 proprotein convertase subtilisin/kexin type 9 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18666258 731024 Pcsk9 proprotein convertase subtilisin/kexin type 9 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18666258 731024 Pcsk9 proprotein convertase subtilisin/kexin type 9 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:18666258 731024 Pcsk9 proprotein convertase subtilisin/kexin type 9 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 731024 Pcsk9 proprotein convertase subtilisin/kexin type 9 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 731029 Sgk1 serum/glucocorticoid regulated kinase 1 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:12417564 731029 Sgk1 serum/glucocorticoid regulated kinase 1 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:18385268 731029 Sgk1 serum/glucocorticoid regulated kinase 1 gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:12417564 731029 Sgk1 serum/glucocorticoid regulated kinase 1 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:18385268 731029 Sgk1 serum/glucocorticoid regulated kinase 1 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:18385268 731029 Sgk1 serum/glucocorticoid regulated kinase 1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200813 MGI PMID:31815093 731029 Sgk1 serum/glucocorticoid regulated kinase 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:12417564 731029 Sgk1 serum/glucocorticoid regulated kinase 1 gene MP:0011442 abnormal renal sodium ion transport IAGP N RGD:5509061 20141003 MGI PMID:12417564 731029 Sgk1 serum/glucocorticoid regulated kinase 1 gene MP:0012046 decreased susceptibility to hypertension IAGP N RGD:5509061 20200813 MGI PMID:31815093 731032 Rgs3 regulator of G-protein signaling 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:24077945 731032 Rgs3 regulator of G-protein signaling 3 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:24077945 731032 Rgs3 regulator of G-protein signaling 3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:24077945 731032 Rgs3 regulator of G-protein signaling 3 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:24077945 731032 Rgs3 regulator of G-protein signaling 3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24077945 731032 Rgs3 regulator of G-protein signaling 3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24077945 731034 Dffb DNA fragmentation factor, beta subunit gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:12524536 731034 Dffb DNA fragmentation factor, beta subunit gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12524536 731034 Dffb DNA fragmentation factor, beta subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12524536 731034 Dffb DNA fragmentation factor, beta subunit gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12524536 731034 Dffb DNA fragmentation factor, beta subunit gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12524536 731034 Dffb DNA fragmentation factor, beta subunit gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12524536 731034 Dffb DNA fragmentation factor, beta subunit gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12524536 731034 Dffb DNA fragmentation factor, beta subunit gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20190718 MGI PMID:25646292 731034 Dffb DNA fragmentation factor, beta subunit gene MP:0004794 increased anti-nuclear antigen antibody level IEA N RGD:5509061 20201022 MGI 731034 Dffb DNA fragmentation factor, beta subunit gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12524536 731034 Dffb DNA fragmentation factor, beta subunit gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12524536 731039 Soat1 sterol O-acyltransferase 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:10777503 731039 Soat1 sterol O-acyltransferase 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:10777503 731039 Soat1 sterol O-acyltransferase 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:8943057 731039 Soat1 sterol O-acyltransferase 1 gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:8943057 731039 Soat1 sterol O-acyltransferase 1 gene MP:0000708 thymus hyperplasia IEA N RGD:5509061 20111116 MGI 731039 Soat1 sterol O-acyltransferase 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:10777503 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:10777503 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:10777503 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10777503 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:10777503 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:10777503 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001337 dry eyes IAGP N RGD:5509061 20141003 MGI PMID:10777503 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001345 Meibomian gland atrophy IAGP N RGD:5509061 20141003 MGI PMID:10777503 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:8943057 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8943057 731039 Soat1 sterol O-acyltransferase 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0002026 increased leukemia incidence IEA N RGD:5509061 20111116 MGI 731039 Soat1 sterol O-acyltransferase 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20141003 MGI 731039 Soat1 sterol O-acyltransferase 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10777503 731039 Soat1 sterol O-acyltransferase 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:8943057 731039 Soat1 sterol O-acyltransferase 1 gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:10777503 731039 Soat1 sterol O-acyltransferase 1 gene MP:0003809 abnormal hair shaft morphology IEA N RGD:5509061 20141003 MGI 731039 Soat1 sterol O-acyltransferase 1 gene MP:0003812 abnormal hair medulla IEA N RGD:5509061 20141003 MGI 731039 Soat1 sterol O-acyltransferase 1 gene MP:0003947 abnormal cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10777503 731039 Soat1 sterol O-acyltransferase 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8943057 731039 Soat1 sterol O-acyltransferase 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8943057 731039 Soat1 sterol O-acyltransferase 1 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:10777503 731039 Soat1 sterol O-acyltransferase 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:10727439 731039 Soat1 sterol O-acyltransferase 1 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:5693089 731039 Soat1 sterol O-acyltransferase 1 gene MP:0008291 abnormal adrenocortical cell morphology IEA N RGD:5509061 20111116 MGI 731039 Soat1 sterol O-acyltransferase 1 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10727439 731041 Hcrt hypocretin gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12750151 731041 Hcrt hypocretin gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:10481909 731041 Hcrt hypocretin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12750151 731041 Hcrt hypocretin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16556901 731041 Hcrt hypocretin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10481909 731041 Hcrt hypocretin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12797957 731041 Hcrt hypocretin gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12797957 731041 Hcrt hypocretin gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:16556901 731041 Hcrt hypocretin gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:10481909 731041 Hcrt hypocretin gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12750151 731041 Hcrt hypocretin gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:10481909 731041 Hcrt hypocretin gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12750151 731041 Hcrt hypocretin gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:16626839 731041 Hcrt hypocretin gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:10481909 731041 Hcrt hypocretin gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:12750151 731041 Hcrt hypocretin gene MP:0004142 abnormal muscle tone IAGP N RGD:5509061 20141003 MGI PMID:21368172 731041 Hcrt hypocretin gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12750151 731041 Hcrt hypocretin gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20221215 MGI 731041 Hcrt hypocretin gene MP:0005279 narcolepsy IAGP N RGD:5509061 20141003 MGI PMID:10481909 731041 Hcrt hypocretin gene MP:0005279 narcolepsy IAGP N RGD:5509061 20141003 MGI PMID:12797957 731041 Hcrt hypocretin gene MP:0005333 decreased heart rate IEA N RGD:5509061 20221215 MGI 731041 Hcrt hypocretin gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:12750151 731041 Hcrt hypocretin gene MP:0008035 behavioral arrest IAGP N RGD:5509061 20141003 MGI PMID:10481909 731041 Hcrt hypocretin gene MP:0009436 fragmentation of sleep/wake states IAGP N RGD:5509061 20141003 MGI PMID:21368172 731041 Hcrt hypocretin gene MP:0009436 fragmentation of sleep/wake states IAGP N RGD:5509061 20220922 MGI PMID:16556901 731041 Hcrt hypocretin gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 731041 Hcrt hypocretin gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220519 MGI 731041 Hcrt hypocretin gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16556901 731041 Hcrt hypocretin gene MP:0012287 increased frequency of paradoxical sleep IAGP N RGD:5509061 20141003 MGI PMID:12797957 731041 Hcrt hypocretin gene MP:0012288 abnormal paradoxical sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12797957 731041 Hcrt hypocretin gene MP:0012289 abnormal non-rapid eye movement sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12797957 731043 Olr1 oxidized low density lipoprotein (lectin-like) receptor 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17478727 731043 Olr1 oxidized low density lipoprotein (lectin-like) receptor 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17478727 731043 Olr1 oxidized low density lipoprotein (lectin-like) receptor 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 731043 Olr1 oxidized low density lipoprotein (lectin-like) receptor 1 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:18022184 731043 Olr1 oxidized low density lipoprotein (lectin-like) receptor 1 gene MP:0004037 increased muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:17478727 731043 Olr1 oxidized low density lipoprotein (lectin-like) receptor 1 gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:18022184 731043 Olr1 oxidized low density lipoprotein (lectin-like) receptor 1 gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17478727 731043 Olr1 oxidized low density lipoprotein (lectin-like) receptor 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17478727 731043 Olr1 oxidized low density lipoprotein (lectin-like) receptor 1 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:17478727 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210826 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0000495 abnormal colon morphology IEA N RGD:5509061 20210826 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22252133 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:11395011 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150618 MGI PMID:15813942 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12000122 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20150618 MGI PMID:15813942 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12000122 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:12000122 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001512 trunk curl IAGP N RGD:5509061 20141003 MGI PMID:11395011 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20201022 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12000122 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11395011 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:11395011 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20150618 MGI PMID:15813942 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:22252133 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:11395011 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11252384 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11395011 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:22252133 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:11395011 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20150618 MGI PMID:15813942 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:22252133 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22252133 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:12000122 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20150618 MGI PMID:15813942 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:11395011 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210128 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20141003 MGI PMID:11395011 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20210826 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0003470 abnormal summary potential IAGP N RGD:5509061 20141003 MGI PMID:12000122 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0003880 abnormal central pattern generator function IAGP N RGD:5509061 20141003 MGI PMID:11395011 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:12000122 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0004002 abnormal jejunum morphology IEA N RGD:5509061 20210826 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:22252133 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22252133 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12000122 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20150618 MGI PMID:18093524 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:11395011 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:22252133 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0005423 abnormal somatic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:11395011 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20150618 MGI PMID:15813942 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20150618 MGI PMID:18093524 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20141003 MGI PMID:22252133 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20150618 MGI PMID:18093524 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0011039 abnormal vestibuloocular dark reflex IAGP N RGD:5509061 20141003 MGI PMID:22252133 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0011040 abnormal vestibuloocular light reflex IAGP N RGD:5509061 20141003 MGI PMID:22252133 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12000122 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11395011 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0011617 abnormal habituation IAGP N RGD:5509061 20150618 MGI PMID:15813942 731045 Slc12a5 solute carrier family 12, member 5 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20150618 MGI PMID:15813942 731049 Cit citron gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20141003 MGI PMID:12432070 731049 Cit citron gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12432070 731049 Cit citron gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12432070 731049 Cit citron gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20160804 MGI 731049 Cit citron gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0009964 abnormal cerebellum lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:11086988 731049 Cit citron gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:12432070 731051 Kcnj15 potassium inwardly-rectifying channel, subfamily J, member 15 gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20141003 MGI 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:19028692 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:19028692 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:19028692 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:19028692 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20150730 MGI PMID:15163627 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20150730 MGI PMID:15163627 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:19028692 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:19028692 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:19028692 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:19028692 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19028692 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:19028692 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19028692 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16595853 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10802663 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:16595853 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:19732742 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:16595853 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19732742 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:10802663 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20150730 MGI PMID:15163627 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0005114 premature hair loss IAGP N RGD:5509061 20141003 MGI PMID:16595853 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:16595853 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16595853 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16595853 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:16595853 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16595853 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:10802663 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16595853 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20150730 MGI PMID:15163627 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20141003 MGI PMID:19028692 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0008861 abnormal hair shedding IAGP N RGD:5509061 20141003 MGI PMID:19028692 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0009297 decreased mammary fat pad weight IAGP N RGD:5509061 20150730 MGI PMID:15163627 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16595853 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20150730 MGI PMID:15163627 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20150730 MGI PMID:15163627 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16595853 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16595853 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20150730 MGI PMID:15163627 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0010249 lactation failure IAGP N RGD:5509061 20150402 MGI PMID:10802663 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0010249 lactation failure IAGP N RGD:5509061 20150730 MGI PMID:15163627 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0011232 abnormal vitamin A level IAGP N RGD:5509061 20141003 MGI PMID:19028692 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:16595853 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0012075 impaired mammary gland growth during pregnancy IAGP N RGD:5509061 20150730 MGI PMID:15163627 731053 Dgat1 diacylglycerol O-acyltransferase 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:16595853 731055 Ephx2 epoxide hydrolase 2, cytoplasmic gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20150122 MGI PMID:24446488 731055 Ephx2 epoxide hydrolase 2, cytoplasmic gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20150122 MGI PMID:24446488 731055 Ephx2 epoxide hydrolase 2, cytoplasmic gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20150122 MGI PMID:24446488 731055 Ephx2 epoxide hydrolase 2, cytoplasmic gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:11001943 731055 Ephx2 epoxide hydrolase 2, cytoplasmic gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11001943 731058 E2f5 E2F transcription factor 5 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9553039 731058 E2f5 E2F transcription factor 5 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:9553039 731058 E2f5 E2F transcription factor 5 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9553039 731058 E2f5 E2F transcription factor 5 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:9553039 731058 E2f5 E2F transcription factor 5 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:9553039 731058 E2f5 E2F transcription factor 5 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:9553039 731058 E2f5 E2F transcription factor 5 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9553039 731058 E2f5 E2F transcription factor 5 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:9553039 731058 E2f5 E2F transcription factor 5 gene MP:0001893 non-obstructive hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:9553039 731058 E2f5 E2F transcription factor 5 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9553039 731058 E2f5 E2F transcription factor 5 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9553039 731058 E2f5 E2F transcription factor 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20160218 MGI PMID:26825228 731058 E2f5 E2F transcription factor 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9553039 731058 E2f5 E2F transcription factor 5 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9553039 731058 E2f5 E2F transcription factor 5 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20160218 MGI PMID:26825228 731058 E2f5 E2F transcription factor 5 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:11030352 731058 E2f5 E2F transcription factor 5 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:9553039 731058 E2f5 E2F transcription factor 5 gene MP:0004728 abnormal efferent ductules of testis morphology IAGP N RGD:5509061 20160218 MGI PMID:26825228 731058 E2f5 E2F transcription factor 5 gene MP:0006423 dilated rete testis IAGP N RGD:5509061 20160218 MGI PMID:26825228 731058 E2f5 E2F transcription factor 5 gene MP:0009257 dilated seminiferous tubule IAGP N RGD:5509061 20160218 MGI PMID:26825228 731058 E2f5 E2F transcription factor 5 gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:9553039 731058 E2f5 E2F transcription factor 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11030352 731058 E2f5 E2F transcription factor 5 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20160218 MGI PMID:26825228 731058 E2f5 E2F transcription factor 5 gene MP:0030316 enlarged neurocranium IAGP N RGD:5509061 20171109 MGI PMID:9553039 731060 Rhoa ras homolog family member A gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:23935982 731060 Rhoa ras homolog family member A gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:21502507 731060 Rhoa ras homolog family member A gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:21502507 731060 Rhoa ras homolog family member A gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21502507 731060 Rhoa ras homolog family member A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191003 MGI PMID:25071083 731060 Rhoa ras homolog family member A gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20191003 MGI PMID:25071083 731060 Rhoa ras homolog family member A gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:21502507 731060 Rhoa ras homolog family member A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23935982 731060 Rhoa ras homolog family member A gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23935982 731060 Rhoa ras homolog family member A gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:23935982 731060 Rhoa ras homolog family member A gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20191003 MGI PMID:25071083 731060 Rhoa ras homolog family member A gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23935982 731060 Rhoa ras homolog family member A gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20191003 MGI PMID:25071083 731060 Rhoa ras homolog family member A gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:21451048 731060 Rhoa ras homolog family member A gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:21502507 731060 Rhoa ras homolog family member A gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:21451048 731060 Rhoa ras homolog family member A gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20200409 MGI PMID:29398449 731060 Rhoa ras homolog family member A gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:21502507 731060 Rhoa ras homolog family member A gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20191003 MGI PMID:25071083 731060 Rhoa ras homolog family member A gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20200409 MGI PMID:29398449 731060 Rhoa ras homolog family member A gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20191003 MGI PMID:25071083 731060 Rhoa ras homolog family member A gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20191003 MGI PMID:25071083 731060 Rhoa ras homolog family member A gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23935982 731060 Rhoa ras homolog family member A gene MP:0009689 abnormal neural tube ventricular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21451048 731060 Rhoa ras homolog family member A gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:21502507 731060 Rhoa ras homolog family member A gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20200409 MGI PMID:29398449 731060 Rhoa ras homolog family member A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21451048 731060 Rhoa ras homolog family member A gene MP:0011402 renal cast IAGP N RGD:5509061 20191003 MGI PMID:25071083 731060 Rhoa ras homolog family member A gene MP:0012091 increased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:21502507 731060 Rhoa ras homolog family member A gene MP:0013182 increased spinal cord apoptosis IAGP N RGD:5509061 20160428 MGI PMID:21451048 731062 Bhlhe41 basic helix-loop-helix family, member e41 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19881507 731062 Bhlhe41 basic helix-loop-helix family, member e41 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19881507 731062 Bhlhe41 basic helix-loop-helix family, member e41 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:19881507 731062 Bhlhe41 basic helix-loop-helix family, member e41 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19881507 731062 Bhlhe41 basic helix-loop-helix family, member e41 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19881507 731062 Bhlhe41 basic helix-loop-helix family, member e41 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19881507 731062 Bhlhe41 basic helix-loop-helix family, member e41 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19881507 731062 Bhlhe41 basic helix-loop-helix family, member e41 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:19881507 731062 Bhlhe41 basic helix-loop-helix family, member e41 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:19881507 731062 Bhlhe41 basic helix-loop-helix family, member e41 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19881507 731062 Bhlhe41 basic helix-loop-helix family, member e41 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19881507 731062 Bhlhe41 basic helix-loop-helix family, member e41 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:19881507 731062 Bhlhe41 basic helix-loop-helix family, member e41 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:18648504 731062 Bhlhe41 basic helix-loop-helix family, member e41 gene MP:0020475 delayed circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:18648504 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:1887865 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:8045348 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:16823860 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:8018921 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000109 abnormal parietal bone morphology IEA N RGD:5509061 20111116 MGI 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9729335 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:1887865 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8018921 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7130905 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8018921 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7130905 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:1887865 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8018921 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:7130905 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:1887865 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20111116 MGI 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:7937762 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:7937762 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:1887865 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:11266447 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:9002639 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:8788202 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11756160 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7130905 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9137093 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001377 abnormal mating frequency IAGP N RGD:5509061 20141003 MGI PMID:9002639 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:8828834 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:9137093 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001562 abnormal circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:9002639 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11756160 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:21791433 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:17218256 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:8018921 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:8018921 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:7937762 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:8828834 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9002639 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20141003 MGI PMID:8788202 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20141003 MGI PMID:9002639 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9002639 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8018921 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:8018921 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:1887865 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:11756160 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:8018921 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:8045348 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002673 abnormal sperm number IAGP N RGD:5509061 20141003 MGI PMID:8828834 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:9002639 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:8788202 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8828834 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:8828834 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:8018921 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20220519 MGI PMID:22527485 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:8045348 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:14613812 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:9002639 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0003357 impaired granulosa cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8788202 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17431224 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16823860 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:17431224 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:1887865 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:7130905 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:8788202 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004235 abnormal masseter muscle morphology IEA N RGD:5509061 20111116 MGI 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004698 abnormal thyroid parafollicular C-cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:8045348 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:8045348 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8045348 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:8828834 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20141003 MGI PMID:8828834 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:1887865 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004983 abnormal osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:8929623 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:11756160 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:8929623 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9137093 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9137093 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16444257 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16823860 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:8018921 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141211 MGI PMID:24633240 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:7937762 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:7937762 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1887865 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008117 abnormal Langerhans cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16444257 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008118 absent Langerhans cell IAGP N RGD:5509061 20141003 MGI PMID:16444257 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008242 abnormal perivascular macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:9729335 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:8045348 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:8427048 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:9002639 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:8787741 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17218256 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:7130905 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:17218256 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17431224 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:9002639 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0009013 abnormal proestrus IAGP N RGD:5509061 20141003 MGI PMID:9002639 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0009090 myometrium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:1887865 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0009091 endometrium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:1887865 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0009325 necrospermia IAGP N RGD:5509061 20141003 MGI PMID:8828834 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:8045348 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0009505 abnormal mammary gland lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:7937762 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20150319 MGI PMID:7937762 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:9002639 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:21389217 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0009971 decreased hippocampus pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:14613812 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20141003 MGI PMID:8045348 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20141003 MGI PMID:8787741 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:11756160 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:1887865 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0010998 pulmonary alveolar proteinosis IAGP N RGD:5509061 20141003 MGI PMID:8018921 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11756160 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:8788202 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0011165 abnormal tooth root development IAGP N RGD:5509061 20141003 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:8787741 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0013586 thymus medulla atrophy IAGP N RGD:5509061 20150319 MGI PMID:1887865 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0030188 round snout IAGP N RGD:5509061 20171019 MGI PMID:16823860 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0030451 abnormal dentin mineralization IAGP N RGD:5509061 20171221 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0030479 increased osteocyte apoptosis IAGP N RGD:5509061 20171221 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0030484 abnormal osteocyte lacuna morphology IAGP N RGD:5509061 20171221 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0030487 abnormal osteocyte dendritic process morphology IAGP N RGD:5509061 20171221 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0030506 abnormal dental follicle morphology IAGP N RGD:5509061 20171228 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0030543 abnormal predentin morphology IAGP N RGD:5509061 20180215 MGI PMID:21958845 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:1262696 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:16823860 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:8018921 731067 Csf1 colony stimulating factor 1 (macrophage) gene MP:0031336 abnormal uterine epithelium development IAGP N RGD:5509061 20220120 MGI PMID:1887865 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0000505 decreased digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:15691866 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:15146045 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:16290192 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:20080609 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:11752469 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15919709 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11856534 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20080609 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:16290192 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:15919709 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:16290192 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:20080609 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12859343 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0004631 abnormal auditory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15721569 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20080609 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0004788 abnormal auditory cortex tonotopy IAGP N RGD:5509061 20141003 MGI PMID:15721569 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:15721569 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:15913791 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0012124 increased bronchoconstrictive response IAGP N RGD:5509061 20141003 MGI PMID:14645675 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0013300 abnormal submandibular gland physiology IAGP N RGD:5509061 20141225 MGI PMID:15146045 731069 Chrm1 cholinergic receptor, muscarinic 1, CNS gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:11752469 731073 Vegfa vascular endothelial growth factor A gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10021335 731073 Vegfa vascular endothelial growth factor A gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:8602241 731073 Vegfa vascular endothelial growth factor A gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20221020 MGI PMID:25759071 731073 Vegfa vascular endothelial growth factor A gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:23178125 731073 Vegfa vascular endothelial growth factor A gene MP:0000262 poor arterial differentiation IAGP N RGD:5509061 20221020 MGI PMID:25759071 731073 Vegfa vascular endothelial growth factor A gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:10952892 731073 Vegfa vascular endothelial growth factor A gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:10952892 731073 Vegfa vascular endothelial growth factor A gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10952892 731073 Vegfa vascular endothelial growth factor A gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:23178125 731073 Vegfa vascular endothelial growth factor A gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:8602242 731073 Vegfa vascular endothelial growth factor A gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:10952892 731073 Vegfa vascular endothelial growth factor A gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20221020 MGI PMID:25759071 731073 Vegfa vascular endothelial growth factor A gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20221020 MGI PMID:25759071 731073 Vegfa vascular endothelial growth factor A gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:10021335 731073 Vegfa vascular endothelial growth factor A gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:12847526 731073 Vegfa vascular endothelial growth factor A gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:12847526 731073 Vegfa vascular endothelial growth factor A gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0000909 abnormal facial motor nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15545635 731073 Vegfa vascular endothelial growth factor A gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:20167862 731073 Vegfa vascular endothelial growth factor A gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:12053176 731073 Vegfa vascular endothelial growth factor A gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17583691 731073 Vegfa vascular endothelial growth factor A gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:12053176 731073 Vegfa vascular endothelial growth factor A gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:12053176 731073 Vegfa vascular endothelial growth factor A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10021335 731073 Vegfa vascular endothelial growth factor A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23178125 731073 Vegfa vascular endothelial growth factor A gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:21654748 731073 Vegfa vascular endothelial growth factor A gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12847526 731073 Vegfa vascular endothelial growth factor A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0001440 abnormal grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:8602242 731073 Vegfa vascular endothelial growth factor A gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0001657 abnormal induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20167862 731073 Vegfa vascular endothelial growth factor A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10021335 731073 Vegfa vascular endothelial growth factor A gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:10952892 731073 Vegfa vascular endothelial growth factor A gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:20167862 731073 Vegfa vascular endothelial growth factor A gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12628185 731073 Vegfa vascular endothelial growth factor A gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10952892 731073 Vegfa vascular endothelial growth factor A gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12053176 731073 Vegfa vascular endothelial growth factor A gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17583691 731073 Vegfa vascular endothelial growth factor A gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:20167862 731073 Vegfa vascular endothelial growth factor A gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12847526 731073 Vegfa vascular endothelial growth factor A gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:20167862 731073 Vegfa vascular endothelial growth factor A gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12053176 731073 Vegfa vascular endothelial growth factor A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17360669 731073 Vegfa vascular endothelial growth factor A gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:10952892 731073 Vegfa vascular endothelial growth factor A gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0002295 abnormal pulmonary circulation IAGP N RGD:5509061 20141003 MGI PMID:17583691 731073 Vegfa vascular endothelial growth factor A gene MP:0002295 abnormal pulmonary circulation IAGP N RGD:5509061 20141003 MGI PMID:20167862 731073 Vegfa vascular endothelial growth factor A gene MP:0002333 abnormal lung compliance IAGP N RGD:5509061 20141003 MGI PMID:20167862 731073 Vegfa vascular endothelial growth factor A gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20160211 MGI PMID:25417109 731073 Vegfa vascular endothelial growth factor A gene MP:0002832 coarse hair IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:8602242 731073 Vegfa vascular endothelial growth factor A gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0003182 decreased pulmonary endothelial cell surface IAGP N RGD:5509061 20141003 MGI PMID:17583691 731073 Vegfa vascular endothelial growth factor A gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21828096 731073 Vegfa vascular endothelial growth factor A gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19261698 731073 Vegfa vascular endothelial growth factor A gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11934854 731073 Vegfa vascular endothelial growth factor A gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:8602241 731073 Vegfa vascular endothelial growth factor A gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:8602242 731073 Vegfa vascular endothelial growth factor A gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:8602242 731073 Vegfa vascular endothelial growth factor A gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:8602242 731073 Vegfa vascular endothelial growth factor A gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0003543 abnormal vascular endothelial cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8602241 731073 Vegfa vascular endothelial growth factor A gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0003653 decreased skin turgor IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:20167862 731073 Vegfa vascular endothelial growth factor A gene MP:0003840 abnormal coronal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0003897 abnormal ST segment IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17583691 731073 Vegfa vascular endothelial growth factor A gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23178125 731073 Vegfa vascular endothelial growth factor A gene MP:0004112 abnormal arteriole morphology IAGP N RGD:5509061 20141003 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0004120 cardiac ischemia IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0004125 abnormal venule morphology IAGP N RGD:5509061 20141003 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0004159 double aortic arch IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0004161 cervical aortic arch IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0004181 abnormal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0004755 abnormal loop of Henle morphology IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:11934854 731073 Vegfa vascular endothelial growth factor A gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:8602241 731073 Vegfa vascular endothelial growth factor A gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:8602242 731073 Vegfa vascular endothelial growth factor A gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:22577176 731073 Vegfa vascular endothelial growth factor A gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:11934854 731073 Vegfa vascular endothelial growth factor A gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0005327 abnormal mesangial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0005327 abnormal mesangial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17583691 731073 Vegfa vascular endothelial growth factor A gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:8602241 731073 Vegfa vascular endothelial growth factor A gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:15545635 731073 Vegfa vascular endothelial growth factor A gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:21828096 731073 Vegfa vascular endothelial growth factor A gene MP:0006057 decreased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:11934854 731073 Vegfa vascular endothelial growth factor A gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:23178125 731073 Vegfa vascular endothelial growth factor A gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141003 MGI PMID:23178125 731073 Vegfa vascular endothelial growth factor A gene MP:0006185 retina hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17583691 731073 Vegfa vascular endothelial growth factor A gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20221020 MGI PMID:25759071 731073 Vegfa vascular endothelial growth factor A gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21828096 731073 Vegfa vascular endothelial growth factor A gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0009392 retina gliosis IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221020 MGI PMID:25759071 731073 Vegfa vascular endothelial growth factor A gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23178125 731073 Vegfa vascular endothelial growth factor A gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:25759071 731073 Vegfa vascular endothelial growth factor A gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20221020 MGI PMID:25759071 731073 Vegfa vascular endothelial growth factor A gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221020 MGI PMID:25759071 731073 Vegfa vascular endothelial growth factor A gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0010453 abnormal coronary vein morphology IAGP N RGD:5509061 20141003 MGI PMID:23178125 731073 Vegfa vascular endothelial growth factor A gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:10952892 731073 Vegfa vascular endothelial growth factor A gene MP:0010458 pulmonary trunk hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0010505 abnormal T wave IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10952892 731073 Vegfa vascular endothelial growth factor A gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23178125 731073 Vegfa vascular endothelial growth factor A gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:10952892 731073 Vegfa vascular endothelial growth factor A gene MP:0010572 persistent right dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0010635 aorta pulmonary collateral arteries IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0010666 abnormal vitelline vein morphology IAGP N RGD:5509061 20150521 MGI PMID:8602242 731073 Vegfa vascular endothelial growth factor A gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:17583691 731073 Vegfa vascular endothelial growth factor A gene MP:0010887 pale lung IAGP N RGD:5509061 20141003 MGI PMID:17583691 731073 Vegfa vascular endothelial growth factor A gene MP:0010911 abnormal pulmonary acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:17583691 731073 Vegfa vascular endothelial growth factor A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10021335 731073 Vegfa vascular endothelial growth factor A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14550787 731073 Vegfa vascular endothelial growth factor A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17583691 731073 Vegfa vascular endothelial growth factor A gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8602241 731073 Vegfa vascular endothelial growth factor A gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11381259 731073 Vegfa vascular endothelial growth factor A gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11934854 731073 Vegfa vascular endothelial growth factor A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8602242 731073 Vegfa vascular endothelial growth factor A gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10952892 731073 Vegfa vascular endothelial growth factor A gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23178125 731073 Vegfa vascular endothelial growth factor A gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0011148 decreased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:17583691 731073 Vegfa vascular endothelial growth factor A gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20150521 MGI PMID:8602242 731073 Vegfa vascular endothelial growth factor A gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0011309 abnormal kidney arterial blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0011312 abnormal kidney afferent arteriole morphology IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0011313 abnormal kidney efferent arteriole morphology IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0011316 abnormal kidney interlobular artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0011321 abnormal peritubular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0011349 abnormal renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0011359 decreased glomerular capillary number IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0011455 absent glomerular endothelium fenestra IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20240118 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0011758 renal ischemia IAGP N RGD:5509061 20141003 MGI PMID:12039984 731073 Vegfa vascular endothelial growth factor A gene MP:0011855 abnormal glomerular filtration barrier morphology IAGP N RGD:5509061 20141003 MGI PMID:12618525 731073 Vegfa vascular endothelial growth factor A gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:11934854 731073 Vegfa vascular endothelial growth factor A gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:8602242 731073 Vegfa vascular endothelial growth factor A gene MP:0012310 persistent ductus caroticus IAGP N RGD:5509061 20141003 MGI PMID:12539040 731073 Vegfa vascular endothelial growth factor A gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20150521 MGI PMID:8602242 731073 Vegfa vascular endothelial growth factor A gene MP:0013164 abnormal forelimb bud morphology IAGP N RGD:5509061 20150521 MGI PMID:8602242 731073 Vegfa vascular endothelial growth factor A gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:8602242 731073 Vegfa vascular endothelial growth factor A gene MP:0020326 dilated capillary IAGP N RGD:5509061 20160714 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0020326 dilated capillary IAGP N RGD:5509061 20160714 MGI PMID:11827992 731073 Vegfa vascular endothelial growth factor A gene MP:0020329 decreased capillary density IAGP N RGD:5509061 20160714 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0020331 increased capillary tortuosity IAGP N RGD:5509061 20160714 MGI PMID:10229225 731073 Vegfa vascular endothelial growth factor A gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:25759071 731073 Vegfa vascular endothelial growth factor A gene MP:0021217 abnormal palatal shelf bone ossification IAGP N RGD:5509061 20230302 MGI PMID:25759071 731073 Vegfa vascular endothelial growth factor A gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20221201 MGI PMID:25759071 731073 Vegfa vascular endothelial growth factor A gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:10229225 731075 Mutyh mutY DNA glycosylase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 731075 Mutyh mutY DNA glycosylase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23143307 731075 Mutyh mutY DNA glycosylase gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 731075 Mutyh mutY DNA glycosylase gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 731075 Mutyh mutY DNA glycosylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15126346 731075 Mutyh mutY DNA glycosylase gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 731075 Mutyh mutY DNA glycosylase gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 731075 Mutyh mutY DNA glycosylase gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 731075 Mutyh mutY DNA glycosylase gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:23143307 731075 Mutyh mutY DNA glycosylase gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 731251 Syt13 synaptotagmin XIII gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20241107 MGI PMID:35927244 731251 Syt13 synaptotagmin XIII gene MP:0011932 abnormal endocrine pancreas development IAGP N RGD:5509061 20241107 MGI PMID:35927244 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:9851981 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:23436999 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9851981 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:15543146 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:18198335 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:15543146 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18198335 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:24174665 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22510201 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23436999 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001260 increased body weight IAGP N RGD:5509061 20241031 MGI PMID:38574733 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9851981 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18713982 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18713982 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:17075007 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17075007 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20231872 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18384748 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20231872 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18384748 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:20231872 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9851981 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:18635610 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18635610 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22510201 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17525802 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:17525802 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:18635610 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:23453624 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20160929 MGI PMID:25803032 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14706336 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17114584 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:18621715 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23453624 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20241031 MGI PMID:38574733 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18621715 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22232209 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:23436999 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:18198335 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23436999 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:20231872 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:20231872 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18384748 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:17075007 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:12185368 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16039563 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20141003 MGI PMID:18198335 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003247 abnormal glutaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18198335 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003334 pancreas fibrosis IAGP N RGD:5509061 20160929 MGI PMID:25803032 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:17114584 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20160929 MGI PMID:25803032 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003338 pancreas lipomatosis IAGP N RGD:5509061 20141003 MGI PMID:22510201 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003341 chronic pancreas inflammation IAGP N RGD:5509061 20160929 MGI PMID:25803032 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20141003 MGI PMID:14706336 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20141003 MGI PMID:23453624 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20160929 MGI PMID:25803032 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:23436999 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:18384748 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17525802 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003655 absent pancreas IAGP N RGD:5509061 20141003 MGI PMID:15543146 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003655 absent pancreas IAGP N RGD:5509061 20141003 MGI PMID:18198335 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003655 absent pancreas IAGP N RGD:5509061 20141003 MGI PMID:23436999 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003655 absent pancreas IAGP N RGD:5509061 20141003 MGI PMID:9851981 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17301087 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20200123 MGI PMID:23926259 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:12185368 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:17938243 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:18635610 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0004155 decreased susceptibility to induced pancreatitis IAGP N RGD:5509061 20241031 MGI PMID:38574733 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:18635610 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:22232209 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:22510201 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0004247 small pancreas IAGP N RGD:5509061 20241031 MGI PMID:38574733 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:23436999 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:24174665 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:24174665 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:18198335 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0005034 abnormal anus morphology IAGP N RGD:5509061 20141003 MGI PMID:23436999 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22232209 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20160929 MGI PMID:25803032 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21903076 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22510201 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:23436999 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17301087 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21903076 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0006095 absent amacrine cells IAGP N RGD:5509061 20141003 MGI PMID:17075007 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0006095 absent amacrine cells IAGP N RGD:5509061 20141003 MGI PMID:17301087 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:18198335 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20240404 MGI PMID:38517960 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0006392 abnormal nucleus pulposus morphology IAGP N RGD:5509061 20141003 MGI PMID:23436999 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0008107 absent retina horizontal cells IAGP N RGD:5509061 20141003 MGI PMID:17075007 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0008508 thick retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:17075007 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0008514 absent retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:17075007 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0008514 absent retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:17301087 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:24174665 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0008579 abnormal Purkinje cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16039563 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:17525802 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17525802 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0008805 decreased circulating amylase level IAGP N RGD:5509061 20141003 MGI PMID:22510201 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:18713982 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009108 increased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:23453624 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009111 pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22510201 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009143 abnormal pancreatic duct morphology IAGP N RGD:5509061 20160929 MGI PMID:25803032 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009144 dilated pancreatic duct IAGP N RGD:5509061 20160929 MGI PMID:25803032 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:18635610 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20160929 MGI PMID:25803032 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20180830 MGI PMID:29670173 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009149 decreased pancreatic acinar cell number IAGP N RGD:5509061 20141003 MGI PMID:18635610 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14706336 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17114584 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18621715 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18713982 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22232209 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23453624 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20150827 MGI PMID:22541435 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20241031 MGI PMID:38574733 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:18621715 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:18713982 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:20473331 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22232209 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:23453624 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20150827 MGI PMID:22541435 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20160929 MGI PMID:25803032 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20161020 MGI PMID:26996122 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20180830 MGI PMID:29670173 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18713982 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22232209 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20161020 MGI PMID:26996122 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20241031 MGI PMID:38574733 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009154 pancreatic acinar hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22510201 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009156 absent pancreatic acini IAGP N RGD:5509061 20141003 MGI PMID:12185368 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009165 abnormal endocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:18635610 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:18635610 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009170 abnormal pancreatic islet size IAGP N RGD:5509061 20141003 MGI PMID:22510201 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:18635610 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:9851981 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009179 abnormal pancreatic alpha cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18635610 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:18635610 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009343 dilated gallbladder IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17525802 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18198335 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0010283 decreased classified tumor incidence IAGP N RGD:5509061 20240404 MGI PMID:38517960 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0010668 abnormal hepatic portal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18635610 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17301087 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18198335 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9851981 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:24174665 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0011934 abnormal branching involved in pancreas development IAGP N RGD:5509061 20141003 MGI PMID:18635610 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0011935 abnormal pancreatic bud formation IAGP N RGD:5509061 20141003 MGI PMID:18635610 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20141003 MGI PMID:17114585 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20141003 MGI PMID:22232209 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20141120 MGI PMID:23453624 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20150827 MGI PMID:22541435 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20160929 MGI PMID:25803032 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20240404 MGI PMID:38517960 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:17114584 731252 Ptf1a pancreas specific transcription factor, 1a gene MP:0031159 abnormal hepatic portal vein thrombosis IAGP N RGD:5509061 20201210 MGI PMID:17114585 731254 Ndufa5 NADH:ubiquinone oxidoreductase subunit A5 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:24154540 731254 Ndufa5 NADH:ubiquinone oxidoreductase subunit A5 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:24154540 731254 Ndufa5 NADH:ubiquinone oxidoreductase subunit A5 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:24154540 731254 Ndufa5 NADH:ubiquinone oxidoreductase subunit A5 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:24154540 731254 Ndufa5 NADH:ubiquinone oxidoreductase subunit A5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24154540 731257 Eif2b2 eukaryotic translation initiation factor 2B, subunit 2 beta gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 731261 Spata2 spermatogenesis associated 2 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20180308 MGI PMID:28701375 731261 Spata2 spermatogenesis associated 2 gene MP:0001147 small testis IAGP N RGD:5509061 20171214 MGI PMID:29025062 731261 Spata2 spermatogenesis associated 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20171214 MGI PMID:29025062 731261 Spata2 spermatogenesis associated 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20180308 MGI PMID:28701375 731261 Spata2 spermatogenesis associated 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20171214 MGI PMID:29025062 731261 Spata2 spermatogenesis associated 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20171214 MGI PMID:29025062 731261 Spata2 spermatogenesis associated 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20171214 MGI PMID:29025062 731261 Spata2 spermatogenesis associated 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20171214 MGI PMID:29025062 731261 Spata2 spermatogenesis associated 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20171214 MGI PMID:29025062 731261 Spata2 spermatogenesis associated 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20231207 MGI 731261 Spata2 spermatogenesis associated 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 731261 Spata2 spermatogenesis associated 2 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20171214 MGI PMID:29025062 731261 Spata2 spermatogenesis associated 2 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20171214 MGI PMID:29025062 731262 Arpc1a actin related protein 2/3 complex, subunit 1A gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20210128 MGI 731262 Arpc1a actin related protein 2/3 complex, subunit 1A gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20210128 MGI 731262 Arpc1a actin related protein 2/3 complex, subunit 1A gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210520 MGI 731262 Arpc1a actin related protein 2/3 complex, subunit 1A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731262 Arpc1a actin related protein 2/3 complex, subunit 1A gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 731265 Polr1b polymerase (RNA) I polypeptide B gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 731265 Polr1b polymerase (RNA) I polypeptide B gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 731265 Polr1b polymerase (RNA) I polypeptide B gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 731265 Polr1b polymerase (RNA) I polypeptide B gene MP:0001200 thick skin IEA N RGD:5509061 20220519 MGI 731265 Polr1b polymerase (RNA) I polypeptide B gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20231207 MGI 731265 Polr1b polymerase (RNA) I polypeptide B gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:18023416 731265 Polr1b polymerase (RNA) I polypeptide B gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210826 MGI 731265 Polr1b polymerase (RNA) I polypeptide B gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:18023416 731265 Polr1b polymerase (RNA) I polypeptide B gene MP:0008830 abnormal nucleolus morphology IAGP N RGD:5509061 20141003 MGI PMID:18023416 731265 Polr1b polymerase (RNA) I polypeptide B gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20180712 MGI PMID:18023416 731265 Polr1b polymerase (RNA) I polypeptide B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 731265 Polr1b polymerase (RNA) I polypeptide B gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 731265 Polr1b polymerase (RNA) I polypeptide B gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 731266 Sra1 steroid receptor RNA activator 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20160421 MGI 731266 Sra1 steroid receptor RNA activator 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141106 MGI PMID:24675075 731266 Sra1 steroid receptor RNA activator 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 731266 Sra1 steroid receptor RNA activator 1 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141106 MGI PMID:24675075 731266 Sra1 steroid receptor RNA activator 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141106 MGI PMID:24675075 731266 Sra1 steroid receptor RNA activator 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141106 MGI PMID:24675075 731266 Sra1 steroid receptor RNA activator 1 gene MP:0002989 small kidney IEA N RGD:5509061 20160811 MGI 731266 Sra1 steroid receptor RNA activator 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141106 MGI PMID:24675075 731266 Sra1 steroid receptor RNA activator 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160421 MGI 731266 Sra1 steroid receptor RNA activator 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141106 MGI PMID:24675075 731266 Sra1 steroid receptor RNA activator 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141106 MGI PMID:24675075 731266 Sra1 steroid receptor RNA activator 1 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141106 MGI PMID:24675075 731266 Sra1 steroid receptor RNA activator 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20181227 MGI 731266 Sra1 steroid receptor RNA activator 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141106 MGI PMID:24675075 731266 Sra1 steroid receptor RNA activator 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141106 MGI PMID:24675075 731266 Sra1 steroid receptor RNA activator 1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141106 MGI PMID:24675075 731266 Sra1 steroid receptor RNA activator 1 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20141106 MGI PMID:24675075 731266 Sra1 steroid receptor RNA activator 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 731266 Sra1 steroid receptor RNA activator 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141106 MGI PMID:24675075 731266 Sra1 steroid receptor RNA activator 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141106 MGI PMID:24675075 731266 Sra1 steroid receptor RNA activator 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 731266 Sra1 steroid receptor RNA activator 1 gene MP:0010360 decreased liver free fatty acids level IAGP N RGD:5509061 20141106 MGI PMID:24675075 731266 Sra1 steroid receptor RNA activator 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:24675075 731268 Pkia protein kinase inhibitor, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10779334 731268 Pkia protein kinase inhibitor, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11359903 731268 Pkia protein kinase inhibitor, alpha gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 731270 Syt2 synaptotagmin II gene MP:0000745 tremors IEA N RGD:5509061 20160915 MGI 731270 Syt2 synaptotagmin II gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16642042 731270 Syt2 synaptotagmin II gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17192432 731270 Syt2 synaptotagmin II gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:17192432 731270 Syt2 synaptotagmin II gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16642042 731270 Syt2 synaptotagmin II gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16642042 731270 Syt2 synaptotagmin II gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17192432 731270 Syt2 synaptotagmin II gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:16642042 731270 Syt2 synaptotagmin II gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17192432 731270 Syt2 synaptotagmin II gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20150122 MGI 731270 Syt2 synaptotagmin II gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17192432 731270 Syt2 synaptotagmin II gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16642042 731270 Syt2 synaptotagmin II gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:17192432 731270 Syt2 synaptotagmin II gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17192432 731270 Syt2 synaptotagmin II gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:17192432 731270 Syt2 synaptotagmin II gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16642042 731270 Syt2 synaptotagmin II gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:16642042 731270 Syt2 synaptotagmin II gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:17192432 731270 Syt2 synaptotagmin II gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:17192432 731270 Syt2 synaptotagmin II gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17192432 731270 Syt2 synaptotagmin II gene MP:0011271 prolonged excitatory postsynaptic current rise time IAGP N RGD:5509061 20240418 MGI PMID:16642042 731275 Pdha2 pyruvate dehydrogenase E1 alpha 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 731276 Cyb5b cytochrome b5 type B gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20240523 MGI 731276 Cyb5b cytochrome b5 type B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 731277 Itgb7 integrin beta 7 gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:10898502 731277 Itgb7 integrin beta 7 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:8684468 731277 Itgb7 integrin beta 7 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:8684468 731277 Itgb7 integrin beta 7 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18439426 731277 Itgb7 integrin beta 7 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18451854 731277 Itgb7 integrin beta 7 gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8684468 731277 Itgb7 integrin beta 7 gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:8684468 731277 Itgb7 integrin beta 7 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:17786243 731277 Itgb7 integrin beta 7 gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:18439426 731277 Itgb7 integrin beta 7 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:17786243 731277 Itgb7 integrin beta 7 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:17786243 731277 Itgb7 integrin beta 7 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:8684468 731277 Itgb7 integrin beta 7 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10898502 731277 Itgb7 integrin beta 7 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8684468 731277 Itgb7 integrin beta 7 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:10898502 731277 Itgb7 integrin beta 7 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15155674 731277 Itgb7 integrin beta 7 gene MP:0008054 abnormal uterine NK cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9421796 731277 Itgb7 integrin beta 7 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8684468 731277 Itgb7 integrin beta 7 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:17786243 731277 Itgb7 integrin beta 7 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:8684468 731277 Itgb7 integrin beta 7 gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:9421796 731277 Itgb7 integrin beta 7 gene MP:0009394 increased uterine NK cell number IAGP N RGD:5509061 20141003 MGI PMID:9421796 731277 Itgb7 integrin beta 7 gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:9421796 731277 Itgb7 integrin beta 7 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:18451854 731277 Itgb7 integrin beta 7 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:8684468 731279 Cyp4x1 cytochrome P450, family 4, subfamily x, polypeptide 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20191114 MGI PMID:29227996 731279 Cyp4x1 cytochrome P450, family 4, subfamily x, polypeptide 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20191219 MGI PMID:29227996 731279 Cyp4x1 cytochrome P450, family 4, subfamily x, polypeptide 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20191219 MGI PMID:29227996 731279 Cyp4x1 cytochrome P450, family 4, subfamily x, polypeptide 1 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20191219 MGI PMID:29227996 731279 Cyp4x1 cytochrome P450, family 4, subfamily x, polypeptide 1 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20191219 MGI PMID:29227996 731279 Cyp4x1 cytochrome P450, family 4, subfamily x, polypeptide 1 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20191219 MGI PMID:29227996 731279 Cyp4x1 cytochrome P450, family 4, subfamily x, polypeptide 1 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20191114 MGI PMID:29227996 731279 Cyp4x1 cytochrome P450, family 4, subfamily x, polypeptide 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20191219 MGI PMID:29227996 731279 Cyp4x1 cytochrome P450, family 4, subfamily x, polypeptide 1 gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20191219 MGI PMID:29227996 731283 Cabp1 calcium binding protein 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20201022 MGI 731283 Cabp1 calcium binding protein 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 731283 Cabp1 calcium binding protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 731283 Cabp1 calcium binding protein 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 731283 Cabp1 calcium binding protein 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20160421 MGI 731283 Cabp1 calcium binding protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:24631676 731283 Cabp1 calcium binding protein 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 731283 Cabp1 calcium binding protein 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20180531 MGI PMID:27822497 731283 Cabp1 calcium binding protein 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20181227 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0000642 enlarged adrenal glands IEA N RGD:5509061 20181227 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:16484321 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:16484321 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16484321 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:16484321 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16484321 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10748062 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:10748062 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20201022 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20201022 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10748062 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11939592 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:14500732 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001513 limb grasping IEA N RGD:5509061 20201022 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:10748062 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:11939592 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:14500732 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:10748062 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10748062 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11939592 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14500732 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10748062 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16484321 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:16484321 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20201231 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11939592 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16484321 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:16484321 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0002637 small uterus IEA N RGD:5509061 20181227 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:11939592 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:15769750 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:14500732 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:14500732 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16484321 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:16484321 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10748062 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14500732 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11939592 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210826 MGI 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0014010 abnormal peroxisome morphology IAGP N RGD:5509061 20200917 MGI PMID:14500732 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:23777740 731285 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:14500732 731292 Bzw2 basic leucine zipper and W2 domains 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 731292 Bzw2 basic leucine zipper and W2 domains 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 731292 Bzw2 basic leucine zipper and W2 domains 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 731292 Bzw2 basic leucine zipper and W2 domains 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220519 MGI 731292 Bzw2 basic leucine zipper and W2 domains 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 731292 Bzw2 basic leucine zipper and W2 domains 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160421 MGI 731292 Bzw2 basic leucine zipper and W2 domains 2 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20201022 MGI 731292 Bzw2 basic leucine zipper and W2 domains 2 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 731292 Bzw2 basic leucine zipper and W2 domains 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160421 MGI 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0000745 tremors IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10021458 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10021458 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:10021458 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11133999 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10021458 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10021458 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:11133999 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10021458 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10021458 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11133999 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:11133999 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11133999 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11133999 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:10021458 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10021458 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:8855236 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:11133999 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0009434 paraparesis IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10021458 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0009978 abnormal cerebellum white matter morphology IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0010734 abnormal paranode morphology IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0010735 abnormal paranodal axoglial junction morphology IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0012231 abnormal ganglioside level IAGP N RGD:5509061 20191010 MGI PMID:15710896 731294 B4galnt1 beta-1,4-N-acetyl-galactosaminyl transferase 1 gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20191010 MGI PMID:15710896 731295 Spa17 sperm autoantigenic protein 17 gene MP:0001925 male infertility IEA N RGD:5509061 20220519 MGI 731295 Spa17 sperm autoantigenic protein 17 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220519 MGI 731295 Spa17 sperm autoantigenic protein 17 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220519 MGI 731298 Dusp6 dual specificity phosphatase 6 gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:17164422 731298 Dusp6 dual specificity phosphatase 6 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17164422 731298 Dusp6 dual specificity phosphatase 6 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17164422 731298 Dusp6 dual specificity phosphatase 6 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18753132 731298 Dusp6 dual specificity phosphatase 6 gene MP:0000275 heart hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18753132 731298 Dusp6 dual specificity phosphatase 6 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17164422 731298 Dusp6 dual specificity phosphatase 6 gene MP:0000730 increased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:22945933 731298 Dusp6 dual specificity phosphatase 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17164422 731298 Dusp6 dual specificity phosphatase 6 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17164422 731298 Dusp6 dual specificity phosphatase 6 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:22945933 731298 Dusp6 dual specificity phosphatase 6 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:18753132 731298 Dusp6 dual specificity phosphatase 6 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:18753132 731298 Dusp6 dual specificity phosphatase 6 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:18753132 731298 Dusp6 dual specificity phosphatase 6 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17164422 731298 Dusp6 dual specificity phosphatase 6 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:18753132 731298 Dusp6 dual specificity phosphatase 6 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17164422 731298 Dusp6 dual specificity phosphatase 6 gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17164422 731298 Dusp6 dual specificity phosphatase 6 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:18753132 731298 Dusp6 dual specificity phosphatase 6 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171207 MGI PMID:17164422 731299 Madcam1 mucosal vascular addressin cell adhesion molecule 1 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:19450594 731299 Madcam1 mucosal vascular addressin cell adhesion molecule 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19450594 731299 Madcam1 mucosal vascular addressin cell adhesion molecule 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19450594 731299 Madcam1 mucosal vascular addressin cell adhesion molecule 1 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:19450594 731299 Madcam1 mucosal vascular addressin cell adhesion molecule 1 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:19450594 731299 Madcam1 mucosal vascular addressin cell adhesion molecule 1 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:19450594 731302 Fnbp1 formin binding protein 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 731302 Fnbp1 formin binding protein 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 731302 Fnbp1 formin binding protein 1 gene MP:0005655 increased aggression IEA N RGD:5509061 20240523 MGI 731304 Rab1a RAB1A, member RAS oncogene family gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20200514 MGI 731304 Rab1a RAB1A, member RAS oncogene family gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:35137917 731304 Rab1a RAB1A, member RAS oncogene family gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20221222 MGI PMID:35137917 731304 Rab1a RAB1A, member RAS oncogene family gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0004971 dermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0010680 abnormal skin adnexa physiology IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:21445300 731308 Rassf9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21445300 731310 Aurkb aurora kinase B gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0003707 increased cell nucleus count IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0009591 increased liver adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:21613325 731310 Aurkb aurora kinase B gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:21613325 731313 Pth1r parathyroid hormone 1 receptor gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21220409 731313 Pth1r parathyroid hormone 1 receptor gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:12050144 731313 Pth1r parathyroid hormone 1 receptor gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12050144 731313 Pth1r parathyroid hormone 1 receptor gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15951842 731313 Pth1r parathyroid hormone 1 receptor gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:12050144 731313 Pth1r parathyroid hormone 1 receptor gene MP:0000168 abnormal bone marrow development IAGP N RGD:5509061 20141003 MGI PMID:15951842 731313 Pth1r parathyroid hormone 1 receptor gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:16840548 731313 Pth1r parathyroid hormone 1 receptor gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:10696074 731313 Pth1r parathyroid hormone 1 receptor gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0001565 abnormal circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:16840548 731313 Pth1r parathyroid hormone 1 receptor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10696074 731313 Pth1r parathyroid hormone 1 receptor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 731313 Pth1r parathyroid hormone 1 receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12050144 731313 Pth1r parathyroid hormone 1 receptor gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10696074 731313 Pth1r parathyroid hormone 1 receptor gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:12050144 731313 Pth1r parathyroid hormone 1 receptor gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:12194850 731313 Pth1r parathyroid hormone 1 receptor gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:12050144 731313 Pth1r parathyroid hormone 1 receptor gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:15951842 731313 Pth1r parathyroid hormone 1 receptor gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:16840548 731313 Pth1r parathyroid hormone 1 receptor gene MP:0002947 increased hemangioma incidence IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12050144 731313 Pth1r parathyroid hormone 1 receptor gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:15951842 731313 Pth1r parathyroid hormone 1 receptor gene MP:0003253 dilated bile duct IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:10696074 731313 Pth1r parathyroid hormone 1 receptor gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10696074 731313 Pth1r parathyroid hormone 1 receptor gene MP:0004053 abnormal synchondrosis IAGP N RGD:5509061 20141003 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:10696074 731313 Pth1r parathyroid hormone 1 receptor gene MP:0004357 long tibia IAGP N RGD:5509061 20141003 MGI PMID:12050144 731313 Pth1r parathyroid hormone 1 receptor gene MP:0004357 long tibia IAGP N RGD:5509061 20141003 MGI PMID:15951842 731313 Pth1r parathyroid hormone 1 receptor gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:16840548 731313 Pth1r parathyroid hormone 1 receptor gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:12050144 731313 Pth1r parathyroid hormone 1 receptor gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:15951842 731313 Pth1r parathyroid hormone 1 receptor gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:15951842 731313 Pth1r parathyroid hormone 1 receptor gene MP:0006429 abnormal hyaline cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15951842 731313 Pth1r parathyroid hormone 1 receptor gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16840548 731313 Pth1r parathyroid hormone 1 receptor gene MP:0009908 protruding tongue IAGP N RGD:5509061 20141003 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0010200 enlarged lymphatic vessel IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0010490 abnormal inferior vena cava valve morphology IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0010912 herniated liver IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10696074 731313 Pth1r parathyroid hormone 1 receptor gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 731313 Pth1r parathyroid hormone 1 receptor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0013846 retropharyngeal edema IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0013864 enlarged paraumbilical vein IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0013876 absent ductus venosus valve IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0013963 jugular vein stenosis IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0014000 anastomosis between internal carotid artery and basilar artery IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 731313 Pth1r parathyroid hormone 1 receptor gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:15951842 731313 Pth1r parathyroid hormone 1 receptor gene MP:0014107 premature chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:12050144 731313 Pth1r parathyroid hormone 1 receptor gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:21220409 731313 Pth1r parathyroid hormone 1 receptor gene MP:0021186 decreased bone mineral density of vertebrae IAGP N RGD:5509061 20220915 MGI PMID:21220409 731313 Pth1r parathyroid hormone 1 receptor gene MP:0030094 foramen magnum stenosis IAGP N RGD:5509061 20170928 MGI PMID:8662561 731313 Pth1r parathyroid hormone 1 receptor gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:29539633 731314 Slc38a1 solute carrier family 38, member 1 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20200723 MGI PMID:31552299 731314 Slc38a1 solute carrier family 38, member 1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20200723 MGI PMID:31552299 731314 Slc38a1 solute carrier family 38, member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 731314 Slc38a1 solute carrier family 38, member 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24062445 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:24062445 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:24062445 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20200611 MGI PMID:30452905 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20200611 MGI PMID:30452905 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24062445 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:24062445 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0003153 early eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:24062445 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:24062445 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20180503 MGI PMID:29625592 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:24062445 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20180503 MGI PMID:29625592 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:24062445 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20180503 MGI PMID:29625592 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20180503 MGI PMID:29625592 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0006265 increased pulse pressure IAGP N RGD:5509061 20180503 MGI PMID:29625592 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20200611 MGI PMID:30452905 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0008579 abnormal Purkinje cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24062445 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20200611 MGI PMID:30452905 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24062445 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0010388 abnormal Bergmann glial cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24062445 731318 Gpr37l1 G protein-coupled receptor 37-like 1 gene MP:0013551 decreased cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20200611 MGI PMID:30452905 731319 Myo1b myosin IB gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20240523 MGI 731321 Ipo13 importin 13 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20180215 MGI PMID:27993670 731322 Fads1 fatty acid desaturase 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170105 MGI 731322 Fads1 fatty acid desaturase 1 gene MP:0001147 small testis IEA N RGD:5509061 20170105 MGI 731322 Fads1 fatty acid desaturase 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 731322 Fads1 fatty acid desaturase 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20160211 MGI 731322 Fads1 fatty acid desaturase 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 731322 Fads1 fatty acid desaturase 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:22534642 731322 Fads1 fatty acid desaturase 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20231207 MGI 731322 Fads1 fatty acid desaturase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22534642 731322 Fads1 fatty acid desaturase 1 gene MP:0002176 increased brain weight IEA N RGD:5509061 20210128 MGI 731322 Fads1 fatty acid desaturase 1 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20231207 MGI 731322 Fads1 fatty acid desaturase 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 731322 Fads1 fatty acid desaturase 1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20210128 MGI 731322 Fads1 fatty acid desaturase 1 gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:22534642 731322 Fads1 fatty acid desaturase 1 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22534642 731322 Fads1 fatty acid desaturase 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 731322 Fads1 fatty acid desaturase 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20160211 MGI 731322 Fads1 fatty acid desaturase 1 gene MP:0008247 abnormal mononuclear cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22534642 731322 Fads1 fatty acid desaturase 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22534642 731322 Fads1 fatty acid desaturase 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22534642 731322 Fads1 fatty acid desaturase 1 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22534642 731322 Fads1 fatty acid desaturase 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22534642 731322 Fads1 fatty acid desaturase 1 gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:22534642 731322 Fads1 fatty acid desaturase 1 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:22534642 731322 Fads1 fatty acid desaturase 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20231207 MGI 731322 Fads1 fatty acid desaturase 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 731322 Fads1 fatty acid desaturase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 731325 Hdgf heparin binding growth factor gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:18570251 731327 Hdac3 histone deacetylase 3 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18830415 731327 Hdac3 histone deacetylase 3 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:18406327 731327 Hdac3 histone deacetylase 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18406327 731327 Hdac3 histone deacetylase 3 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:18830415 731327 Hdac3 histone deacetylase 3 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18830415 731327 Hdac3 histone deacetylase 3 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:18830415 731327 Hdac3 histone deacetylase 3 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20190321 MGI PMID:30626716 731327 Hdac3 histone deacetylase 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20190321 MGI PMID:30626716 731327 Hdac3 histone deacetylase 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18830415 731327 Hdac3 histone deacetylase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23192980 731327 Hdac3 histone deacetylase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23192980 731327 Hdac3 histone deacetylase 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:24268577 731327 Hdac3 histone deacetylase 3 gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:18830415 731327 Hdac3 histone deacetylase 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:18830415 731327 Hdac3 histone deacetylase 3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18406327 731327 Hdac3 histone deacetylase 3 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20190321 MGI PMID:30626716 731327 Hdac3 histone deacetylase 3 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20190321 MGI PMID:30626716 731327 Hdac3 histone deacetylase 3 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:23192980 731327 Hdac3 histone deacetylase 3 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20141003 MGI PMID:18830415 731327 Hdac3 histone deacetylase 3 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18830415 731327 Hdac3 histone deacetylase 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18406327 731327 Hdac3 histone deacetylase 3 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20150212 MGI PMID:18406327 731327 Hdac3 histone deacetylase 3 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0009662 abnormal uterine receptivity IAGP N RGD:5509061 20190321 MGI PMID:30626716 731327 Hdac3 histone deacetylase 3 gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20190321 MGI PMID:30626716 731327 Hdac3 histone deacetylase 3 gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20190321 MGI PMID:30626716 731327 Hdac3 histone deacetylase 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:18354499 731327 Hdac3 histone deacetylase 3 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:18830415 731327 Hdac3 histone deacetylase 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23192980 731327 Hdac3 histone deacetylase 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18406327 731327 Hdac3 histone deacetylase 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18830415 731327 Hdac3 histone deacetylase 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731327 Hdac3 histone deacetylase 3 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:18830415 731327 Hdac3 histone deacetylase 3 gene MP:0013399 endometrium fibrosis IAGP N RGD:5509061 20190321 MGI PMID:30626716 731327 Hdac3 histone deacetylase 3 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:18406327 731327 Hdac3 histone deacetylase 3 gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:18830415 731327 Hdac3 histone deacetylase 3 gene MP:0014368 enhanced long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:21228185 731327 Hdac3 histone deacetylase 3 gene MP:0020253 increased collagen level IAGP N RGD:5509061 20190321 MGI PMID:30626716 731327 Hdac3 histone deacetylase 3 gene MP:0031418 increased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:18830415 731327 Hdac3 histone deacetylase 3 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:18830415 731330 Rcan1 regulator of calcineurin 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12515860 731330 Rcan1 regulator of calcineurin 1 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:16648267 731330 Rcan1 regulator of calcineurin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16648267 731330 Rcan1 regulator of calcineurin 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16648267 731330 Rcan1 regulator of calcineurin 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:16648267 731330 Rcan1 regulator of calcineurin 1 gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20141003 MGI PMID:18180251 731330 Rcan1 regulator of calcineurin 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16648267 731330 Rcan1 regulator of calcineurin 1 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16648267 731330 Rcan1 regulator of calcineurin 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:16648267 731330 Rcan1 regulator of calcineurin 1 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12515860 731330 Rcan1 regulator of calcineurin 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16648267 731330 Rcan1 regulator of calcineurin 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:19458618 731330 Rcan1 regulator of calcineurin 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:17341486 731330 Rcan1 regulator of calcineurin 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 731330 Rcan1 regulator of calcineurin 1 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:12515860 731330 Rcan1 regulator of calcineurin 1 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:16648267 731330 Rcan1 regulator of calcineurin 1 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16648267 731330 Rcan1 regulator of calcineurin 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12925851 731330 Rcan1 regulator of calcineurin 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16648267 731330 Rcan1 regulator of calcineurin 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16648267 731330 Rcan1 regulator of calcineurin 1 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:19620774 731330 Rcan1 regulator of calcineurin 1 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16648267 731330 Rcan1 regulator of calcineurin 1 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:12925851 731330 Rcan1 regulator of calcineurin 1 gene MP:0006412 abnormal T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12925851 731330 Rcan1 regulator of calcineurin 1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12925851 731330 Rcan1 regulator of calcineurin 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12925851 731330 Rcan1 regulator of calcineurin 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:19620774 731330 Rcan1 regulator of calcineurin 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 731332 Slc36a2 solute carrier family 36 (proton/amino acid symporter), member 2 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20201022 MGI 731332 Slc36a2 solute carrier family 36 (proton/amino acid symporter), member 2 gene MP:0005655 increased aggression IEA N RGD:5509061 20201022 MGI 731333 Bmp3 bone morphogenetic protein 3 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20220922 MGI PMID:11138004 731333 Bmp3 bone morphogenetic protein 3 gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:11138004 731334 Arf2 ADP-ribosylation factor 2 gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 731334 Arf2 ADP-ribosylation factor 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160421 MGI 731334 Arf2 ADP-ribosylation factor 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 731334 Arf2 ADP-ribosylation factor 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 731334 Arf2 ADP-ribosylation factor 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 731336 Kcnv1 potassium channel, subfamily V, member 1 gene MP:0000743 muscle spasm IEA N RGD:5509061 20111116 MGI 731336 Kcnv1 potassium channel, subfamily V, member 1 gene MP:0000745 tremors IEA N RGD:5509061 20111116 MGI 731336 Kcnv1 potassium channel, subfamily V, member 1 gene MP:0001393 ataxia IEA N RGD:5509061 20111116 MGI 731336 Kcnv1 potassium channel, subfamily V, member 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 731336 Kcnv1 potassium channel, subfamily V, member 1 gene MP:0004222 iris synechia IEA N RGD:5509061 20190502 MGI 731342 Utrn utrophin gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10559919 731342 Utrn utrophin gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:10559919 731342 Utrn utrophin gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10204788 731342 Utrn utrophin gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:10719885 731342 Utrn utrophin gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:9049252 731342 Utrn utrophin gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:9049253 731342 Utrn utrophin gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20705734 731342 Utrn utrophin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:20705734 731342 Utrn utrophin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10559919 731342 Utrn utrophin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10559919 731342 Utrn utrophin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:10559919 731342 Utrn utrophin gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12028357 731342 Utrn utrophin gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:10559919 731342 Utrn utrophin gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0004036 abnormal muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0004510 myositis IAGP N RGD:5509061 20160929 MGI PMID:17889902 731342 Utrn utrophin gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:9049253 731342 Utrn utrophin gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:10559919 731342 Utrn utrophin gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:9288752 731342 Utrn utrophin gene MP:0009398 abnormal skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:20705734 731342 Utrn utrophin gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:9288751 731342 Utrn utrophin gene MP:0009420 skeletal muscle endomysial fibrosis IAGP N RGD:5509061 20160929 MGI PMID:17889902 731342 Utrn utrophin gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12028357 731342 Utrn utrophin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10559919 731342 Utrn utrophin gene MP:0013467 diaphragmitis IAGP N RGD:5509061 20160929 MGI PMID:17889902 731344 Nmt1 N-myristoyltransferase 1 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0008600 decreased circulating interleukin-2 level IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0009335 decreased splenocyte proliferation IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20151203 MGI PMID:26423150 731344 Nmt1 N-myristoyltransferase 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15888483 731344 Nmt1 N-myristoyltransferase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15888483 731344 Nmt1 N-myristoyltransferase 1 gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20151203 MGI PMID:26423150 731345 Necab2 N-terminal EF-hand calcium binding protein 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20160915 MGI PMID:24652767 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21189261 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20170216 MGI PMID:25602015 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17343295 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20210819 MGI PMID:30478397 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20210819 MGI PMID:30478397 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:21189261 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20170216 MGI PMID:25602015 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20170216 MGI PMID:25602015 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17343295 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0003596 epididymis inflammation IAGP N RGD:5509061 20141003 MGI PMID:21189261 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20170216 MGI PMID:25602015 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20170216 MGI PMID:25602015 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20170216 MGI PMID:25602015 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21189261 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141030 MGI PMID:24402311 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20210819 MGI PMID:30478397 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:21189261 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20141003 MGI PMID:21189261 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141030 MGI PMID:24402311 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141030 MGI PMID:24402311 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141030 MGI PMID:24402311 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:21189261 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20210819 MGI PMID:30478397 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0009233 enlarged sperm head IAGP N RGD:5509061 20141003 MGI PMID:21189261 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0009236 pinhead sperm IAGP N RGD:5509061 20141003 MGI PMID:21189261 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:21189261 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20210819 MGI PMID:30478397 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20170216 MGI PMID:25602015 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20210819 MGI PMID:30478397 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20210819 MGI PMID:30478397 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20210819 MGI PMID:30478397 731346 Ido1 indoleamine 2,3-dioxygenase 1 gene MP:0030603 increased sperm number IAGP N RGD:5509061 20180621 MGI PMID:21189261 731350 Bex3 brain expressed X-linked 3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230119 MGI 731350 Bex3 brain expressed X-linked 3 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 731350 Bex3 brain expressed X-linked 3 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 731350 Bex3 brain expressed X-linked 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 731350 Bex3 brain expressed X-linked 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 731350 Bex3 brain expressed X-linked 3 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 731350 Bex3 brain expressed X-linked 3 gene MP:0002801 abnormal long-term object recognition memory IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 731350 Bex3 brain expressed X-linked 3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230119 MGI 731350 Bex3 brain expressed X-linked 3 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0004375 enlarged frontal bone IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0005386 behavior/neurological phenotype IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0006212 large orbits IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0011151 abnormal hippocampus stratum radiatum morphology IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20230216 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:33100228 731350 Bex3 brain expressed X-linked 3 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20230216 MGI PMID:33100228 731351 Atp5f1d ATP synthase F1 subunit delta gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241010 MGI 731351 Atp5f1d ATP synthase F1 subunit delta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230720 MGI 731351 Atp5f1d ATP synthase F1 subunit delta gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241010 MGI 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20160915 MGI PMID:27355534 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20160915 MGI PMID:27355534 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20220825 MGI PMID:27117872 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:21427221 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20210325 MGI PMID:30942852 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21427221 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:21427221 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:21427221 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0001934 increased litter size IAGP N RGD:5509061 20210325 MGI PMID:30942852 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21427221 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:21427221 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21427221 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20160915 MGI PMID:27355534 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20160915 MGI PMID:27355534 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:21427221 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20160915 MGI PMID:27355534 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20160915 MGI PMID:27355534 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20160915 MGI PMID:27355534 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0006133 calcified artery IAGP N RGD:5509061 20141003 MGI PMID:21427221 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20160915 MGI PMID:27355534 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20160915 MGI PMID:27355534 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0008870 increased mature ovarian follicle number IAGP N RGD:5509061 20210325 MGI PMID:30942852 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20220825 MGI PMID:27117872 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20220825 MGI PMID:27117872 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20160915 MGI PMID:27355534 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0010932 increased trabecular bone connectivity density IAGP N RGD:5509061 20220825 MGI PMID:27117872 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0010962 decreased compact bone mass IAGP N RGD:5509061 20220825 MGI PMID:27117872 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0012072 decreased susceptibility to osteoporosis IAGP N RGD:5509061 20220825 MGI PMID:27117872 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20160915 MGI PMID:27355534 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20220825 MGI PMID:27117872 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160915 MGI PMID:27355534 731352 Sfrp4 secreted frizzled-related protein 4 gene MP:0031411 increased ovulation rate IAGP N RGD:5509061 20220804 MGI PMID:30942852 731357 Akap1 A kinase anchor protein 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:16461287 731357 Akap1 A kinase anchor protein 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:16461287 731357 Akap1 A kinase anchor protein 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:16461287 731358 Bdkrb1 bradykinin receptor, beta 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 731358 Bdkrb1 bradykinin receptor, beta 1 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20210128 MGI 731358 Bdkrb1 bradykinin receptor, beta 1 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:10859349 731358 Bdkrb1 bradykinin receptor, beta 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16497152 731358 Bdkrb1 bradykinin receptor, beta 1 gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:10859349 731358 Bdkrb1 bradykinin receptor, beta 1 gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20141003 MGI PMID:10859349 731358 Bdkrb1 bradykinin receptor, beta 1 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:10859349 731358 Bdkrb1 bradykinin receptor, beta 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 731358 Bdkrb1 bradykinin receptor, beta 1 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:10859349 731358 Bdkrb1 bradykinin receptor, beta 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16497152 731358 Bdkrb1 bradykinin receptor, beta 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16497152 731358 Bdkrb1 bradykinin receptor, beta 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16497152 731358 Bdkrb1 bradykinin receptor, beta 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 731358 Bdkrb1 bradykinin receptor, beta 1 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20210128 MGI 731365 Gtf2b general transcription factor IIB gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 731365 Gtf2b general transcription factor IIB gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 731365 Gtf2b general transcription factor IIB gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 731369 Tff2 trefoil factor 2 (spasmolytic protein 1) gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:11805131 731369 Tff2 trefoil factor 2 (spasmolytic protein 1) gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:11805131 731369 Tff2 trefoil factor 2 (spasmolytic protein 1) gene MP:0000503 excessive digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:11805131 731369 Tff2 trefoil factor 2 (spasmolytic protein 1) gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:16121031 731369 Tff2 trefoil factor 2 (spasmolytic protein 1) gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:16121031 731369 Tff2 trefoil factor 2 (spasmolytic protein 1) gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:16121031 731369 Tff2 trefoil factor 2 (spasmolytic protein 1) gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:11805131 731369 Tff2 trefoil factor 2 (spasmolytic protein 1) gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:11805131 731371 Exoc7 exocyst complex component 7 gene MP:0005159 azoospermia IAGP N RGD:5509061 20240530 MGI PMID:38325858 731371 Exoc7 exocyst complex component 7 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20240530 MGI PMID:38325858 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17067568 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0003445 sirenomelia IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0003445 sirenomelia IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0003605 fused kidneys IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17067568 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0003942 abnormal urinary system development IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0008786 abnormal hindgut morphology IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0009798 abnormal ophthalmic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0009799 abnormal maxillary nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0010116 abnormal primitive urogenital sinus morphology IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11157777 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0011361 pelvic kidney IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0011772 genital tubercle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0012798 increased rhombomere 4 size IAGP N RGD:5509061 20141003 MGI PMID:11157778 731376 Cyp26a1 cytochrome P450, family 26, subfamily a, polypeptide 1 gene MP:0012818 rhombomere transformation IAGP N RGD:5509061 20141003 MGI PMID:11157778 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12837930 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23624557 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:11375261 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0002664 decreased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:12642666 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0002987 abnormal urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:9843913 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:19940926 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20141003 MGI PMID:12837930 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20141003 MGI PMID:17676060 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20141003 MGI PMID:19940926 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20141003 MGI PMID:9751056 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:12642666 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0005525 increased renal plasma flow rate IAGP N RGD:5509061 20141003 MGI PMID:11123248 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0005530 decreased renal vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:11123248 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:11123248 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23624557 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12837930 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:17676060 731379 Ptger3 prostaglandin E receptor 3 (subtype EP3) gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201224 MGI PMID:17242161 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:15933268 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20171116 MGI PMID:18791645 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0000416 sparse hair IEA N RGD:5509061 20111116 MGI 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0000418 focal hair loss IEA N RGD:5509061 20111116 MGI 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0000745 tremors IEA N RGD:5509061 20111116 MGI 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:16788063 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16917506 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:12353028 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12353028 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12353028 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20141003 MGI PMID:15703386 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20171116 MGI PMID:18791645 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20171116 MGI PMID:18791645 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20171116 MGI PMID:18791645 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20171116 MGI PMID:18791645 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20171116 MGI PMID:18791645 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15933268 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15933268 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16788063 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20171116 MGI PMID:18791645 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20111116 MGI 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0002083 premature death IAGP N RGD:5509061 20171116 MGI PMID:18791645 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:15933268 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15933268 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:15933268 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:12353028 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16917506 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15703386 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16917506 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15933268 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:12353028 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:15933268 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12353028 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12353028 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:15933268 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15933268 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:16917506 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12353028 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11279485 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:16917506 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:16917506 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0006039 decreased mitochondrial fission IAGP N RGD:5509061 20141003 MGI PMID:16917506 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16917506 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12353028 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0008103 amacrine cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12353028 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:15703386 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:12353028 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:12353028 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:12353028 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0008775 abnormal heart ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20171116 MGI PMID:18791645 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15933268 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:16788063 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20171116 MGI PMID:18791645 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16788063 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16788063 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16917506 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0011593 increased catalase activity IAGP N RGD:5509061 20141003 MGI PMID:12353028 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0011593 increased catalase activity IAGP N RGD:5509061 20171116 MGI PMID:18791645 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0011594 decreased catalase activity IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:16788063 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0012660 increased superoxide dismutase level IAGP N RGD:5509061 20171116 MGI PMID:18791645 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:16287843 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16788063 731381 Aifm1 apoptosis-inducing factor, mitochondrion-associated 1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:12353028 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000015 abnormal ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1490901 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000015 abnormal ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:5473311 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:5473311 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:5473311 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:1490901 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:5473311 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19100679 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20536544 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:5929249 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:20536544 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:24805242 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:12754375 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:12354381 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:7621074 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:15024050 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:15067126 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:19124833 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:22101159 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:7683920 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:8605335 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:16467148 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000370 head blaze IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000370 head blaze IAGP N RGD:5509061 20141003 MGI PMID:9006068 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:16577810 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:4392283 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:469229 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:7683920 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:7704626 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17246829 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4392283 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:469229 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:10932191 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:15820307 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:19917283 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:20095975 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:20536544 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:22367038 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:4392283 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:469229 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:9006068 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000373 belly spot IAGP N RGD:5509061 20181227 MGI PMID:18641651 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18098338 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000467 abnormal esophagus morphology IAGP N RGD:5509061 20141003 MGI PMID:12754375 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000467 abnormal esophagus morphology IAGP N RGD:5509061 20141003 MGI PMID:18098338 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:12754375 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15067126 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15067126 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19100679 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:12354381 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11226047 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11226047 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001128 ovary hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11226047 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001143 constricted vagina orifice IEA N RGD:5509061 20111116 MGI 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12406368 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:8951075 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10655061 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15024050 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:7704626 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:12754375 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001189 absent skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:20095975 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:7704626 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:19917283 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:5929249 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7621074 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20171116 MGI PMID:14869351 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17246829 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19917283 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12393491 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12406368 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:1692559 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:6628990 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7704626 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9006068 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001586 abnormal erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:5929249 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001586 abnormal erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7117838 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7621074 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001619 abnormal vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:23624557 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:11438492 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:6510711 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15067126 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7621074 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15024050 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:16180252 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16709868 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:12754375 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16577810 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12406368 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:20095975 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:20095975 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10655061 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:1692559 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:1692559 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10655061 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:7000343 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002016 ovary cyst IAGP N RGD:5509061 20161222 MGI PMID:27354067 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14871802 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10932191 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15067126 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16577810 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17246829 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:22367038 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4392283 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7117838 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8605335 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20171116 MGI PMID:14869351 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20536544 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:469229 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10560917 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12754375 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14871802 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15067126 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18098338 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20161222 MGI PMID:27354067 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11438492 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7117838 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12354381 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15024050 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12354381 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15024050 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002213 true hermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:8951075 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10655061 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:20536544 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:12817015 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:19100679 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15024050 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7683920 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:7621074 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20512127 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:20512127 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:20512127 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:19100679 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:5929249 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20230511 MGI PMID:21553221 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002593 high mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:5929249 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12354381 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002606 increased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20512127 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002607 decreased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22101159 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:5929249 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20230511 MGI PMID:21553221 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20201022 MGI PMID:32499443 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002671 belted IAGP N RGD:5509061 20141003 MGI PMID:18454205 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12406368 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20141003 MGI PMID:10655061 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12406368 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:20512127 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24825397 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002810 microcytic anemia IEA N RGD:5509061 20111116 MGI 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:15393917 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:20536544 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:4392283 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:469229 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:6628990 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:7117838 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:7565742 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:8898216 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20171116 MGI PMID:14869351 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:5473311 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:5473311 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:20512127 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20536544 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19100679 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20536544 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7117838 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7683920 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:1490901 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22367038 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8898216 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20141003 MGI PMID:5473311 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:10932191 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:15067126 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:1692559 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:18454205 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:19917283 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:20095975 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:20536544 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:469221 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:5929249 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:7565742 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:7683920 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:8898216 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002939 head spot IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002939 head spot IAGP N RGD:5509061 20141003 MGI PMID:4392283 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002939 head spot IAGP N RGD:5509061 20141003 MGI PMID:469229 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:12444107 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:14170406 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:16577810 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:17246829 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:6510711 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:7619726 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:7704626 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:16180252 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20141003 MGI PMID:8136523 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20141003 MGI PMID:8898216 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:16467148 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:12867261 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20230511 MGI PMID:21553221 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003143 enlarged otoliths IAGP N RGD:5509061 20141003 MGI PMID:5473311 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:5473311 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003175 reversion by mitotic recombination IAGP N RGD:5509061 20141003 MGI PMID:7565742 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003277 increased esophageal papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:7000343 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20141003 MGI PMID:23535651 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003301 peptic ulcer IAGP N RGD:5509061 20141003 MGI PMID:7000343 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:22101159 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20161222 MGI PMID:27354067 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:23535651 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:12817015 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17923505 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:19100679 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:20536544 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003705 abnormal hypodermis morphology IAGP N RGD:5509061 20141003 MGI PMID:7704626 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:20536544 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:8898216 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004034 belly blaze IEA N RGD:5509061 20111116 MGI 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:20536544 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:5473311 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004364 thin stria vascularis IAGP N RGD:5509061 20141003 MGI PMID:1490901 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004364 thin stria vascularis IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004364 thin stria vascularis IAGP N RGD:5509061 20141003 MGI PMID:5473311 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004365 abnormal strial basal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1490901 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004366 abnormal strial marginal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1490901 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004368 abnormal stria vascularis vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:1490901 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004368 abnormal stria vascularis vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004368 abnormal stria vascularis vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:5473311 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22367038 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:5473311 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004410 absent endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:1490901 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:20512127 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:20512127 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:10560917 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12406368 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:12406368 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0004935 epididymis degeneration IAGP N RGD:5509061 20230601 MGI PMID:37095084 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15067126 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7621074 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12354381 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15024050 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20512127 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:7621074 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:20664169 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9510253 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:10560917 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:1490901 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005077 abnormal melanogenesis IAGP N RGD:5509061 20141003 MGI PMID:14871802 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:7621074 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:7621074 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005159 azoospermia IAGP N RGD:5509061 20190228 MGI PMID:8491376 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15067126 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1692559 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17246829 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:20095975 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:6628990 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7117838 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7619726 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7683920 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7704626 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005175 non-pigmented tail tip IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005175 non-pigmented tail tip IAGP N RGD:5509061 20141003 MGI PMID:469229 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005175 non-pigmented tail tip IAGP N RGD:5509061 20141003 MGI PMID:8898216 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16180252 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:9438424 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:8605335 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005535 abnormal body temperature IAGP N RGD:5509061 20141003 MGI PMID:23624557 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:20536544 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20230511 MGI PMID:21553221 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23624557 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20230518 MGI PMID:30563839 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:6696991 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:20536544 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005652 sex reversal IAGP N RGD:5509061 20141003 MGI PMID:8951075 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:367470 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:23535651 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0006010 absent strial intermediate cells IAGP N RGD:5509061 20141003 MGI PMID:1490901 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0006010 absent strial intermediate cells IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:5473311 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0006361 abnormal female germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8898216 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12406368 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:7621074 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12393491 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7621074 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20161222 MGI PMID:27354067 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008031 decreased Cajal-Retzius cell number IAGP N RGD:5509061 20141003 MGI PMID:9438424 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:7621074 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:7621074 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008237 abnormal ventral coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15024050 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7621074 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15067126 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008391 abnormal primordial germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8136523 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:20512127 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:12817015 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:16709868 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:16709868 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:12754375 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:20004959 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008770 decreased survivor rate IEA N RGD:5509061 20111116 MGI 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19100679 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:11226047 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19100679 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0008976 delayed female fertility IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009205 abnormal internal male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:8951075 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:15067126 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009361 abnormal primordial ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20536544 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009379 abnormal foot pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009476 enlarged cecum IAGP N RGD:5509061 20141003 MGI PMID:12754375 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009477 small cecum IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009480 distended cecum IAGP N RGD:5509061 20141003 MGI PMID:12754375 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009485 distended ileum IAGP N RGD:5509061 20141003 MGI PMID:12754375 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009485 distended ileum IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009485 distended ileum IAGP N RGD:5509061 20141003 MGI PMID:18098338 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009511 distended stomach IAGP N RGD:5509061 20141003 MGI PMID:18098338 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009515 increased gastrointestinal stromal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12754375 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009515 increased gastrointestinal stromal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009515 increased gastrointestinal stromal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18098338 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009536 abnormal interstitial cell of Cajal morphology IAGP N RGD:5509061 20141003 MGI PMID:11438492 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009536 abnormal interstitial cell of Cajal morphology IAGP N RGD:5509061 20141003 MGI PMID:19917283 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009537 interstitial cells of Cajal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12754375 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009537 interstitial cells of Cajal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20004959 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16180252 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17923505 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17923505 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19100679 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:9006068 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009784 abnormal melanoblast migration IAGP N RGD:5509061 20141003 MGI PMID:8898216 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009854 impaired gastric peristalsis IAGP N RGD:5509061 20141003 MGI PMID:23535651 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:7704626 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0010016 variable depigmentation IAGP N RGD:5509061 20141003 MGI PMID:15067126 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0010215 abnormal circulating complement protein level IAGP N RGD:5509061 20141003 MGI PMID:20512127 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14871802 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0010389 mosaic coat color IAGP N RGD:5509061 20141003 MGI PMID:14871802 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0010769 abnormal survival IAGP N RGD:5509061 20171116 MGI PMID:14869351 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0010801 abnormal myenteric nerve plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:12754375 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22652566 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011082 abnormal gastrointestinal motility IAGP N RGD:5509061 20141003 MGI PMID:23535651 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15067126 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17246829 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6628990 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17612398 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6510711 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12406368 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24805242 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8898216 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15067126 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7565742 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20171116 MGI PMID:14869351 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14170406 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19917283 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6510711 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IEA N RGD:5509061 20111116 MGI 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IEA N RGD:5509061 20111116 MGI 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6628990 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7274658 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12393491 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8951075 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8951075 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20171116 MGI PMID:14869351 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:11226047 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10716931 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:19100679 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011188 increased erythrocyte protoporphyrin level IAGP N RGD:5509061 20141003 MGI PMID:658175 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011277 decreased tail pigmentation IEA N RGD:5509061 20111116 MGI 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011279 decreased ear pigmentation IEA N RGD:5509061 20111116 MGI 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:16180252 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011696 absent mast cells IAGP N RGD:5509061 20141003 MGI PMID:7704626 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15731517 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20161222 MGI PMID:27354067 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0013539 increased ovary adenoma incidence IAGP N RGD:5509061 20161222 MGI PMID:27354067 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:14871802 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:16061643 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20230518 MGI PMID:30563839 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0030757 abnormal circulating histamine level IAGP N RGD:5509061 20180927 MGI PMID:23624557 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0030934 decreased primordial germ cell proliferation IAGP N RGD:5509061 20190411 MGI PMID:8136523 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0031276 abnormal stress erythropoiesis IAGP N RGD:5509061 20210805 MGI PMID:19100679 731383 Kit KIT proto-oncogene receptor tyrosine kinase gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:10716931 731386 Dapk3 death-associated protein kinase 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 731386 Dapk3 death-associated protein kinase 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20150917 MGI PMID:25304685 731386 Dapk3 death-associated protein kinase 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20240523 MGI 731386 Dapk3 death-associated protein kinase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150917 MGI PMID:25304685 731386 Dapk3 death-associated protein kinase 3 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20240523 MGI 731386 Dapk3 death-associated protein kinase 3 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20150917 MGI PMID:25304685 731386 Dapk3 death-associated protein kinase 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 731386 Dapk3 death-associated protein kinase 3 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20220519 MGI 731389 Slc23a1 solute carrier family 23 (nucleobase transporters), member 1 gene MP:0001671 abnormal vitamin absorption IAGP N RGD:5509061 20141003 MGI PMID:20200446 731389 Slc23a1 solute carrier family 23 (nucleobase transporters), member 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20200446 731389 Slc23a1 solute carrier family 23 (nucleobase transporters), member 1 gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:20200446 731389 Slc23a1 solute carrier family 23 (nucleobase transporters), member 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:20200446 731389 Slc23a1 solute carrier family 23 (nucleobase transporters), member 1 gene MP:0004019 abnormal vitamin homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20200446 731389 Slc23a1 solute carrier family 23 (nucleobase transporters), member 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:20200446 731389 Slc23a1 solute carrier family 23 (nucleobase transporters), member 1 gene MP:0005556 abnormal renal filtration rate IAGP N RGD:5509061 20141003 MGI PMID:20200446 731389 Slc23a1 solute carrier family 23 (nucleobase transporters), member 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:20200446 731389 Slc23a1 solute carrier family 23 (nucleobase transporters), member 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20200446 731389 Slc23a1 solute carrier family 23 (nucleobase transporters), member 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20200446 731389 Slc23a1 solute carrier family 23 (nucleobase transporters), member 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20200446 731389 Slc23a1 solute carrier family 23 (nucleobase transporters), member 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20200446 731389 Slc23a1 solute carrier family 23 (nucleobase transporters), member 1 gene MP:0011229 abnormal vitamin C level IAGP N RGD:5509061 20141003 MGI PMID:20200446 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:14623826 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16556915 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:21898763 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:16556915 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:12397115 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15475956 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:16556915 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:12397115 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000299 failure of atrioventricular cushion closure IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000299 failure of atrioventricular cushion closure IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:15475956 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12441290 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:12441290 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:15475956 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:21898763 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001147 small testis IEA N RGD:5509061 20200402 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21964592 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:16203745 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:16203745 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001296 macrophthalmia IEA N RGD:5509061 20190207 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:20568247 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20141003 MGI PMID:21898763 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:20568247 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:20568247 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:20568247 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:20568247 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001317 abnormal pupil morphology IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20141003 MGI PMID:20568247 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16203745 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:16203745 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12397115 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:16556915 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:20457925 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:21898763 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:21898763 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12397115 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20201231 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:21898763 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12397115 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:12441290 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002649 abnormal enamel rod pattern IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002659 pituitary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002659 pituitary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21898763 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12397115 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:14623826 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:12397115 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002728 absent tibia IAGP N RGD:5509061 20141003 MGI PMID:12441290 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16556915 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:15475956 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:21964592 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:14623826 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:16203745 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20568247 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003686 abnormal eye muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003687 abnormal intraocular muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:20568247 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003727 abnormal retina layer morphology IEA N RGD:5509061 20190207 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003818 abnormal eye muscle development IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003818 abnormal eye muscle development IAGP N RGD:5509061 20141003 MGI PMID:16203745 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0003932 abnormal molar crown morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004021 abnormal rod electrophysiology IEA N RGD:5509061 20190207 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004022 abnormal cone electrophysiology IEA N RGD:5509061 20190207 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:17994097 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:12397115 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15475956 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004159 double aortic arch IAGP N RGD:5509061 20141003 MGI PMID:12397115 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:11807026 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:20568247 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004224 absent trabecular meshwork IAGP N RGD:5509061 20141003 MGI PMID:20568247 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:16203745 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004283 absent cornea endothelium IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004349 absent femur IAGP N RGD:5509061 20141003 MGI PMID:12441290 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004575 small limb buds IAGP N RGD:5509061 20141003 MGI PMID:12441290 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0004673 splayed ribs IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0005102 abnormal iris pigmentation IEA N RGD:5509061 20190207 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16203745 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:21964592 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11807026 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:11807026 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0005247 abnormal extraocular muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0005258 ocular hypertension IEA N RGD:5509061 20190207 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16556915 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20568247 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0005497 optic nerve cupping IEA N RGD:5509061 20190207 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0005551 abnormal eye electrophysiology IEA N RGD:5509061 20190207 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:21898763 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006062 abnormal vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006062 abnormal vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006064 abnormal superior vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16556915 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:17994097 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006198 enophthalmos IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20568247 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006240 anisocoria IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006241 abnormal placement of pupils IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006241 abnormal placement of pupils IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:17994097 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0006400 decreased molar number IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20170105 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0008329 decreased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:11807026 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0008336 absent gonadotrophs IAGP N RGD:5509061 20141003 MGI PMID:11807026 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0008338 decreased thyrotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:11807026 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0008365 adenohypophysis hypoplasia IAGP N RGD:5509061 20141218 MGI PMID:11807026 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0008543 atrial fibrillation IAGP N RGD:5509061 20141003 MGI PMID:20457925 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0008726 increased heart left atrium size IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0009490 abnormal heart left atrium auricular region morphology IAGP N RGD:5509061 20141003 MGI PMID:21089073 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0009829 enlarged eye anterior chamber IEA N RGD:5509061 20190207 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:14975719 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010096 abnormal incisor color IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:20457925 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12397115 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15475956 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16556915 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:16556915 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010406 common atrium IAGP N RGD:5509061 20231221 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21089073 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010425 abnormal heart and great vessel attachment IAGP N RGD:5509061 20141003 MGI PMID:16556915 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010426 abnormal heart and great artery attachment IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010437 absent coronary sinus IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010440 anomalous pulmonary venous connection IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010440 anomalous pulmonary venous connection IAGP N RGD:5509061 20141003 MGI PMID:12397115 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010440 anomalous pulmonary venous connection IAGP N RGD:5509061 20141003 MGI PMID:16556915 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010459 supravalvar pulmonary trunk stenosis IAGP N RGD:5509061 20141003 MGI PMID:16556915 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16556915 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:16556915 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010668 abnormal hepatic portal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010709 absent eye anterior chamber IAGP N RGD:5509061 20201119 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010710 absent sclera IAGP N RGD:5509061 20141003 MGI PMID:16203745 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0010807 abnormal stomach position or orientation IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12397115 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16556915 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011481 anterior iris synechia IEA N RGD:5509061 20190207 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011569 abnormal azygos vein morphology IAGP N RGD:5509061 20141003 MGI PMID:16835440 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11493526 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20190207 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0012144 decreased b-wave amplitude IEA N RGD:5509061 20190207 MGI 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0012273 axial mesoderm hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0012535 abnormal optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0012536 delayed optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0013169 small hindlimb buds IAGP N RGD:5509061 20141003 MGI PMID:12441290 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0013337 abnormal adenohypophysis development IAGP N RGD:5509061 20141211 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0013349 small Rathke's pouch IAGP N RGD:5509061 20141218 MGI PMID:11807026 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:11807026 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:15761027 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0013352 abnormal Rathke's pouch apoptosis IAGP N RGD:5509061 20141218 MGI PMID:15761027 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0013742 absent ciliary body IAGP N RGD:5509061 20150416 MGI PMID:20568247 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0020854 increased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0030026 small Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:14623826 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0030038 abnormal periorbital region morphology IAGP N RGD:5509061 20170928 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0030039 abnormal facial muscle morphology IAGP N RGD:5509061 20170928 MGI PMID:10499586 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0030171 absent extraocular muscles IAGP N RGD:5509061 20171005 MGI PMID:10499585 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0030171 absent extraocular muscles IAGP N RGD:5509061 20171005 MGI PMID:10572050 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0030494 abnormal molar root morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0030496 taurodontia IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0030525 abnormal Hertwig epithelial root sheath morphology IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20180125 MGI PMID:10498698 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0030544 abnormal enamel development IAGP N RGD:5509061 20190711 MGI PMID:27369589 731391 Pitx2 paired-like homeodomain transcription factor 2 gene MP:0030579 thoracoabdominoschisis IAGP N RGD:5509061 20180607 MGI PMID:10499586 731393 Fstl3 follistatin-like 3 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 731393 Fstl3 follistatin-like 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 731393 Fstl3 follistatin-like 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20181227 MGI 731393 Fstl3 follistatin-like 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20181227 MGI 731393 Fstl3 follistatin-like 3 gene MP:0001148 enlarged testis IEA N RGD:5509061 20181227 MGI 731393 Fstl3 follistatin-like 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0003820 increased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:20810712 731393 Fstl3 follistatin-like 3 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:17229845 731393 Fstl3 follistatin-like 3 gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:17229845 731394 F2rl3 F2R like thrombin or trypsin receptor 3 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:12384423 731394 F2rl3 F2R like thrombin or trypsin receptor 3 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:16434493 731394 F2rl3 F2R like thrombin or trypsin receptor 3 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:12384423 731396 Vcan versican gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9188753 731396 Vcan versican gene MP:0000269 abnormal heart looping IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20151119 MGI PMID:22692047 731396 Vcan versican gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:9188753 731396 Vcan versican gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20151119 MGI PMID:22692047 731396 Vcan versican gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:20404343 731396 Vcan versican gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:19922873 731396 Vcan versican gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:19922873 731396 Vcan versican gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:20404343 731396 Vcan versican gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0001217 absent epidermis IAGP N RGD:5509061 20231130 MGI PMID:31669737 731396 Vcan versican gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20231130 MGI PMID:31669737 731396 Vcan versican gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0001297 microphthalmia IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20151119 MGI PMID:22692047 731396 Vcan versican gene MP:0001575 cyanosis IAGP N RGD:5509061 20151119 MGI PMID:22692047 731396 Vcan versican gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9188753 731396 Vcan versican gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20231130 MGI PMID:31669737 731396 Vcan versican gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0001914 hemorrhage IAGP N RGD:5509061 20231130 MGI PMID:31669737 731396 Vcan versican gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:20404343 731396 Vcan versican gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20404343 731396 Vcan versican gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20231130 MGI PMID:31669737 731396 Vcan versican gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:9188753 731396 Vcan versican gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:9188753 731396 Vcan versican gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9188753 731396 Vcan versican gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20151119 MGI PMID:22692047 731396 Vcan versican gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:9188753 731396 Vcan versican gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:20404343 731396 Vcan versican gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19535585 731396 Vcan versican gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20404343 731396 Vcan versican gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20151119 MGI PMID:22692047 731396 Vcan versican gene MP:0010586 absent conotruncal ridges IAGP N RGD:5509061 20141003 MGI PMID:9188753 731396 Vcan versican gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20151119 MGI PMID:22692047 731396 Vcan versican gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9188753 731396 Vcan versican gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20151119 MGI PMID:22692047 731396 Vcan versican gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20151119 MGI PMID:22692047 731396 Vcan versican gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20231130 MGI PMID:31669737 731396 Vcan versican gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20240307 MGI 731396 Vcan versican gene MP:0014283 hindlimb syndactyly IAGP N RGD:5509061 20231130 MGI PMID:31669737 731397 Hdgfl2 HDGF like 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20141003 MGI 731397 Hdgfl2 HDGF like 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 731397 Hdgfl2 HDGF like 2 gene MP:0011704 decreased fibroblast proliferation IEA N RGD:5509061 20141003 MGI 731399 Pfkl phosphofructokinase, liver, B-type gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20190124 MGI PMID:25340873 731399 Pfkl phosphofructokinase, liver, B-type gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20190124 MGI PMID:25340873 731399 Pfkl phosphofructokinase, liver, B-type gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20190124 MGI PMID:25340873 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:14499647 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:16332269 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:24142516 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15936750 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:15936750 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24142516 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000384 distorted hair follicle pattern IAGP N RGD:5509061 20141003 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:16332269 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:21041656 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:24142516 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001194 dermatitis IAGP N RGD:5509061 20181122 MGI PMID:25902485 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20181122 MGI PMID:25902485 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:20976179 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21041656 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:14993236 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:16332269 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:17709479 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:24142516 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20161103 MGI PMID:25918388 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001316 cornea scarring IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20976179 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20976179 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:14993236 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20181122 MGI PMID:25902485 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20161103 MGI PMID:25918388 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20160804 MGI 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17709479 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:24142516 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18762577 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17709479 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20181122 MGI PMID:25902485 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:17709479 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:23354118 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:24142516 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:23354118 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:23354118 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:17709479 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002748 abnormal pulmonary valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002748 abnormal pulmonary valve morphology IAGP N RGD:5509061 20141003 MGI PMID:17709479 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20181122 MGI PMID:25902485 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:14499647 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:23354118 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:14499647 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0003153 early eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20161103 MGI PMID:25918388 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:14499647 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0003711 pathological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0003853 dry skin IAGP N RGD:5509061 20181122 MGI PMID:25902485 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:23354118 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:24142516 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:14499647 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0004226 absent Schlemm's canal IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0004283 absent cornea endothelium IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0004285 absent Descemet membrane IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0004391 abnormal respiratory conducting tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0004545 enlarged esophagus IAGP N RGD:5509061 20141003 MGI PMID:16332269 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:14499647 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20976179 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:23354118 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0005204 abnormal canal of Schlemm morphology IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15936750 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24142516 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:20644114 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:23354118 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0006236 absent Meibomian glands IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24142516 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20181122 MGI PMID:25902485 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20181122 MGI PMID:25902485 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:21041656 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17709479 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:21041656 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17709479 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:21041656 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20141003 MGI PMID:24142516 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008838 decreased transforming growth factor beta level IAGP N RGD:5509061 20141003 MGI PMID:21041656 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21628404 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20161103 MGI PMID:25918388 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:19201862 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:20976179 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0009859 eye opacity IAGP N RGD:5509061 20141003 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010072 increased pruritus IAGP N RGD:5509061 20181122 MGI PMID:25902485 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20160922 MGI PMID:24652767 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20181122 MGI PMID:25902485 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20181122 MGI PMID:25902485 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20160922 MGI PMID:24652767 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15936750 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:23354118 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010591 enlarged aortic valve IAGP N RGD:5509061 20141003 MGI PMID:12773386 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010591 enlarged aortic valve IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010591 enlarged aortic valve IAGP N RGD:5509061 20161103 MGI PMID:25918388 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20141003 MGI PMID:23354118 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20161103 MGI PMID:25918388 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20141003 MGI PMID:15936750 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010595 abnormal aortic valve cusp morphology IAGP N RGD:5509061 20141003 MGI PMID:23354118 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010600 enlarged pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010600 enlarged pulmonary valve IAGP N RGD:5509061 20231221 MGI PMID:12773386 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010605 thick pulmonary valve cusps IAGP N RGD:5509061 20161103 MGI PMID:25918388 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010614 abnormal mitral valve cusp morphology IAGP N RGD:5509061 20231221 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010620 thick mitral valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010626 thick tricuspid valve cusps IAGP N RGD:5509061 20161103 MGI PMID:25918388 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010629 thick tricuspid valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:24142516 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20160922 MGI PMID:24652767 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010887 pale lung IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0010897 abnormal bronchiole epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17709479 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20603312 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23354118 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24142516 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23354118 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15936750 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20976179 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20644114 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:11254358 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:24142516 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011481 anterior iris synechia IAGP N RGD:5509061 20150430 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0011929 abnormal aortic valve flow IAGP N RGD:5509061 20141003 MGI PMID:23354118 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0012269 nuchal edema IAGP N RGD:5509061 20231221 MGI PMID:20976179 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0013744 abnormal conjunctival sac morphology IAGP N RGD:5509061 20150416 MGI PMID:9812885 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0013745 abnormal eyelid margin morphology IAGP N RGD:5509061 20150416 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0020333 enhanced leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:21628404 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0031563 pulmonary valve hypertrophy IAGP N RGD:5509061 20240125 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0031569 aortic valve hypertrophy IAGP N RGD:5509061 20240125 MGI PMID:20194968 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0031570 enlarged atrioventricular valve IAGP N RGD:5509061 20240125 MGI PMID:12773386 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0031580 enlarged semilunar valve IAGP N RGD:5509061 20240125 MGI PMID:12773386 731401 Adam17 a disintegrin and metallopeptidase domain 17 gene MP:0031580 enlarged semilunar valve IAGP N RGD:5509061 20240125 MGI PMID:23354118 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000130 abnormal trabecular bone morphology IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000135 decreased compact bone thickness IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15153675 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9662403 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:9662403 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20220616 MGI PMID:22095884 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:15153675 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9662403 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000154 rib fusion IAGP N RGD:5509061 20220616 MGI PMID:22095884 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000160 kyphosis IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000162 lordosis IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000547 short limbs IEA N RGD:5509061 20150910 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:15153675 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000589 thin tail IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:15153675 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000755 hindlimb paralysis IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9662403 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9662403 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:15153675 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:9662403 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:9662403 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0001935 decreased litter size IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20150910 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15153675 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0002566 abnormal sexual interaction IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0002907 abnormal parturition IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0003047 abnormal thoracic vertebrae morphology IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0003048 abnormal cervical vertebrae morphology IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0003049 abnormal lumbar vertebrae morphology IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0003051 curly tail IEA N RGD:5509061 20150910 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0003794 delayed somite formation IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0004206 abnormal dermomyotome development IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:15153675 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20220616 MGI PMID:22095884 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0004626 vertebral compression IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0004645 decreased vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0004673 splayed ribs IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0004704 short vertebral column IEA N RGD:5509061 20111116 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:9662403 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0006029 abnormal sclerotome morphology IEA N RGD:5509061 20111229 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15153675 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0008317 abnormal paravertebral ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:9662403 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0010082 sternebra fusion IEA N RGD:5509061 20141003 MGI 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:9662403 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0012182 abnormal presomitic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9662403 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0012669 abnormal somite segmentation clock IAGP N RGD:5509061 20141003 MGI PMID:11923214 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0012728 abnormal somite border morphology IAGP N RGD:5509061 20141003 MGI PMID:9662403 731402 Dll3 delta like canonical Notch ligand 3 gene MP:0021138 abnormal multifidus muscle morphology IAGP N RGD:5509061 20220630 MGI PMID:22095884 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15314154 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15314154 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15314154 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:24150605 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:24150605 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20220804 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24150605 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0003572 abnormal uterus development IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0005158 ovary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15314154 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:24150605 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15314154 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15314154 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:24150605 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:24150605 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:24150605 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0011130 absent tertiary ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24150605 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:11940664 731403 Sh2b1 SH2B adaptor protein 1 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:11940664 731407 Scg5 secretogranin V gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0000192 abnormal mineral level IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20230601 MGI 731407 Scg5 secretogranin V gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 731407 Scg5 secretogranin V gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 731407 Scg5 secretogranin V gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 731407 Scg5 secretogranin V gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 731407 Scg5 secretogranin V gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0002163 abnormal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 731407 Scg5 secretogranin V gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230601 MGI 731407 Scg5 secretogranin V gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 731407 Scg5 secretogranin V gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0003960 increased lean body mass IEA N RGD:5509061 20231207 MGI 731407 Scg5 secretogranin V gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 731407 Scg5 secretogranin V gene MP:0005129 increased adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0008299 adrenal cortical hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0009275 bruising IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0009276 ecchymosis IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10089884 731407 Scg5 secretogranin V gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:12021197 731407 Scg5 secretogranin V gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 731410 Il6st interleukin 6 signal transducer gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16679075 731410 Il6st interleukin 6 signal transducer gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14755335 731410 Il6st interleukin 6 signal transducer gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:14755335 731410 Il6st interleukin 6 signal transducer gene MP:0000168 abnormal bone marrow development IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12423677 731410 Il6st interleukin 6 signal transducer gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9815272 731410 Il6st interleukin 6 signal transducer gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21148800 731410 Il6st interleukin 6 signal transducer gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12423677 731410 Il6st interleukin 6 signal transducer gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9815272 731410 Il6st interleukin 6 signal transducer gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:9815272 731410 Il6st interleukin 6 signal transducer gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9815272 731410 Il6st interleukin 6 signal transducer gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:8552649 731410 Il6st interleukin 6 signal transducer gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:12219085 731410 Il6st interleukin 6 signal transducer gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:12219085 731410 Il6st interleukin 6 signal transducer gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:14755335 731410 Il6st interleukin 6 signal transducer gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:15761498 731410 Il6st interleukin 6 signal transducer gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12219085 731410 Il6st interleukin 6 signal transducer gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:9815272 731410 Il6st interleukin 6 signal transducer gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:9815272 731410 Il6st interleukin 6 signal transducer gene MP:0000997 abnormal synovial joint capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9815272 731410 Il6st interleukin 6 signal transducer gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8552649 731410 Il6st interleukin 6 signal transducer gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:14699500 731410 Il6st interleukin 6 signal transducer gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8552649 731410 Il6st interleukin 6 signal transducer gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9815272 731410 Il6st interleukin 6 signal transducer gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20150702 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8552649 731410 Il6st interleukin 6 signal transducer gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18641358 731410 Il6st interleukin 6 signal transducer gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:14699500 731410 Il6st interleukin 6 signal transducer gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10205167 731410 Il6st interleukin 6 signal transducer gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:9815272 731410 Il6st interleukin 6 signal transducer gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9815272 731410 Il6st interleukin 6 signal transducer gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0002224 abnormal spleen size IAGP N RGD:5509061 20170608 MGI PMID:26974160 731410 Il6st interleukin 6 signal transducer gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12423677 731410 Il6st interleukin 6 signal transducer gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:16286017 731410 Il6st interleukin 6 signal transducer gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9815272 731410 Il6st interleukin 6 signal transducer gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:9815272 731410 Il6st interleukin 6 signal transducer gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:9815272 731410 Il6st interleukin 6 signal transducer gene MP:0002658 abnormal liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:18216023 731410 Il6st interleukin 6 signal transducer gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0002936 joint swelling IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:14755335 731410 Il6st interleukin 6 signal transducer gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:12423677 731410 Il6st interleukin 6 signal transducer gene MP:0003282 gastric ulcer IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0003300 gastrointestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0003432 increased activity of parathyroid IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0003486 abnormal channel response intensity IAGP N RGD:5509061 20141003 MGI PMID:17961593 731410 Il6st interleukin 6 signal transducer gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:19109195 731410 Il6st interleukin 6 signal transducer gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16679075 731410 Il6st interleukin 6 signal transducer gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:12219085 731410 Il6st interleukin 6 signal transducer gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:17961593 731410 Il6st interleukin 6 signal transducer gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0004361 bowed ulna IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0004371 bowed femur IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0004372 bowed fibula IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0004373 bowed humerus IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:8552649 731410 Il6st interleukin 6 signal transducer gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:14755335 731410 Il6st interleukin 6 signal transducer gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:14755335 731410 Il6st interleukin 6 signal transducer gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0005002 abnormal T cell clonal deletion IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:16679075 731410 Il6st interleukin 6 signal transducer gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0005211 increased stomach mucosa thickness IAGP N RGD:5509061 20170608 MGI PMID:26974160 731410 Il6st interleukin 6 signal transducer gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9815272 731410 Il6st interleukin 6 signal transducer gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20231207 MGI 731410 Il6st interleukin 6 signal transducer gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:17961593 731410 Il6st interleukin 6 signal transducer gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 731410 Il6st interleukin 6 signal transducer gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:15292206 731410 Il6st interleukin 6 signal transducer gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12423677 731410 Il6st interleukin 6 signal transducer gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20141003 MGI PMID:14699500 731410 Il6st interleukin 6 signal transducer gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:14755335 731410 Il6st interleukin 6 signal transducer gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12423677 731410 Il6st interleukin 6 signal transducer gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12423677 731410 Il6st interleukin 6 signal transducer gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12097503 731410 Il6st interleukin 6 signal transducer gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20170713 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:12370259 731410 Il6st interleukin 6 signal transducer gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:12219085 731410 Il6st interleukin 6 signal transducer gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:12219085 731410 Il6st interleukin 6 signal transducer gene MP:0008542 enlarged cervical lymph nodes IAGP N RGD:5509061 20170713 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21148800 731410 Il6st interleukin 6 signal transducer gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21148800 731410 Il6st interleukin 6 signal transducer gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21148800 731410 Il6st interleukin 6 signal transducer gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:21148800 731410 Il6st interleukin 6 signal transducer gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:21148800 731410 Il6st interleukin 6 signal transducer gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:8552649 731410 Il6st interleukin 6 signal transducer gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12219085 731410 Il6st interleukin 6 signal transducer gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12219085 731410 Il6st interleukin 6 signal transducer gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:8552649 731410 Il6st interleukin 6 signal transducer gene MP:0009216 abnormal peritoneum morphology IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:14755335 731410 Il6st interleukin 6 signal transducer gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:16679075 731410 Il6st interleukin 6 signal transducer gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8552649 731410 Il6st interleukin 6 signal transducer gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20150702 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0009623 enlarged inguinal lymph nodes IAGP N RGD:5509061 20170713 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0009631 enlarged axillary lymph nodes IAGP N RGD:5509061 20170713 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15761498 731410 Il6st interleukin 6 signal transducer gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12219085 731410 Il6st interleukin 6 signal transducer gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21148800 731410 Il6st interleukin 6 signal transducer gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:16679075 731410 Il6st interleukin 6 signal transducer gene MP:0010270 decreased stomach tumor incidence IAGP N RGD:5509061 20170608 MGI PMID:26974160 731410 Il6st interleukin 6 signal transducer gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20170608 MGI PMID:26974160 731410 Il6st interleukin 6 signal transducer gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12219085 731410 Il6st interleukin 6 signal transducer gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14699500 731410 Il6st interleukin 6 signal transducer gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16041381 731410 Il6st interleukin 6 signal transducer gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:10205167 731410 Il6st interleukin 6 signal transducer gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:12219085 731410 Il6st interleukin 6 signal transducer gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:14699500 731410 Il6st interleukin 6 signal transducer gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20170608 MGI PMID:26974160 731410 Il6st interleukin 6 signal transducer gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11457894 731410 Il6st interleukin 6 signal transducer gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14617570 731410 Il6st interleukin 6 signal transducer gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8552649 731410 Il6st interleukin 6 signal transducer gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731410 Il6st interleukin 6 signal transducer gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10661409 731410 Il6st interleukin 6 signal transducer gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9815272 731410 Il6st interleukin 6 signal transducer gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 731410 Il6st interleukin 6 signal transducer gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:16679075 731410 Il6st interleukin 6 signal transducer gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:16679075 731410 Il6st interleukin 6 signal transducer gene MP:0030863 decreased joint mobility IAGP N RGD:5509061 20181101 MGI PMID:11457894 731414 Grk1 G protein-coupled receptor kinase 1 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:12853434 731414 Grk1 G protein-coupled receptor kinase 1 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10097103 731414 Grk1 G protein-coupled receptor kinase 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10097103 731414 Grk1 G protein-coupled receptor kinase 1 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10097103 731414 Grk1 G protein-coupled receptor kinase 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:10097103 731414 Grk1 G protein-coupled receptor kinase 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200116 MGI PMID:26427409 731414 Grk1 G protein-coupled receptor kinase 1 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200116 MGI PMID:26427409 731414 Grk1 G protein-coupled receptor kinase 1 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200116 MGI PMID:26427409 731414 Grk1 G protein-coupled receptor kinase 1 gene MP:0012671 retina spots IAGP N RGD:5509061 20200116 MGI PMID:26427409 731414 Grk1 G protein-coupled receptor kinase 1 gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:10097103 731416 Csf3 colony stimulating factor 3 (granulocyte) gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7521686 731416 Csf3 colony stimulating factor 3 (granulocyte) gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:7521686 731416 Csf3 colony stimulating factor 3 (granulocyte) gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7521686 731416 Csf3 colony stimulating factor 3 (granulocyte) gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19918056 731416 Csf3 colony stimulating factor 3 (granulocyte) gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7521686 731416 Csf3 colony stimulating factor 3 (granulocyte) gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19918056 731416 Csf3 colony stimulating factor 3 (granulocyte) gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:7521686 731416 Csf3 colony stimulating factor 3 (granulocyte) gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:7521686 731416 Csf3 colony stimulating factor 3 (granulocyte) gene MP:0002608 increased hematocrit IEA N RGD:5509061 20230601 MGI 731416 Csf3 colony stimulating factor 3 (granulocyte) gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230601 MGI 731416 Csf3 colony stimulating factor 3 (granulocyte) gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:19918056 731416 Csf3 colony stimulating factor 3 (granulocyte) gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20230601 MGI 731416 Csf3 colony stimulating factor 3 (granulocyte) gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20230601 MGI 731419 Klhl12 kelch-like 12 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 731419 Klhl12 kelch-like 12 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 731419 Klhl12 kelch-like 12 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201022 MGI 731419 Klhl12 kelch-like 12 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20220519 MGI 731424 Doc2a double C2, alpha gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10594652 731424 Doc2a double C2, alpha gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:10594652 731424 Doc2a double C2, alpha gene MP:0002915 abnormal synaptic depression IAGP N RGD:5509061 20241031 MGI PMID:33753311 731424 Doc2a double C2, alpha gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:20150444 731424 Doc2a double C2, alpha gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20241031 MGI PMID:33753311 731424 Doc2a double C2, alpha gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20150444 731424 Doc2a double C2, alpha gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20241031 MGI PMID:33753311 731424 Doc2a double C2, alpha gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20241031 MGI PMID:33753311 731424 Doc2a double C2, alpha gene MP:0008921 increased neurotransmitter release IAGP N RGD:5509061 20241031 MGI PMID:33753311 731424 Doc2a double C2, alpha gene MP:0014253 decreased paired-pulse ratio IAGP N RGD:5509061 20241031 MGI PMID:33753311 731427 Rpl24 ribosomal protein L24 gene MP:0000373 belly spot IAGP N RGD:5509061 20220721 MGI PMID:35013307 731427 Rpl24 ribosomal protein L24 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:10049578 731427 Rpl24 ribosomal protein L24 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:10049578 731427 Rpl24 ribosomal protein L24 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:8589526 731427 Rpl24 ribosomal protein L24 gene MP:0000592 short tail IAGP N RGD:5509061 20220721 MGI PMID:35013307 731427 Rpl24 ribosomal protein L24 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10049578 731427 Rpl24 ribosomal protein L24 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20141003 MGI PMID:8589526 731427 Rpl24 ribosomal protein L24 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15289434 731427 Rpl24 ribosomal protein L24 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220721 MGI PMID:35013307 731427 Rpl24 ribosomal protein L24 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:10681427 731427 Rpl24 ribosomal protein L24 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:10681427 731427 Rpl24 ribosomal protein L24 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:10681427 731427 Rpl24 ribosomal protein L24 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:15289434 731427 Rpl24 ribosomal protein L24 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10049578 731427 Rpl24 ribosomal protein L24 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:15289434 731427 Rpl24 ribosomal protein L24 gene MP:0002697 abnormal eye size IAGP N RGD:5509061 20141003 MGI PMID:10049578 731427 Rpl24 ribosomal protein L24 gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:8589526 731427 Rpl24 ribosomal protein L24 gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15289434 731427 Rpl24 ribosomal protein L24 gene MP:0003099 retina detachment IAGP N RGD:5509061 20141003 MGI PMID:10681427 731427 Rpl24 ribosomal protein L24 gene MP:0003099 retina detachment IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0003711 pathological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:10681427 731427 Rpl24 ribosomal protein L24 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:10049578 731427 Rpl24 ribosomal protein L24 gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:15289434 731427 Rpl24 ribosomal protein L24 gene MP:0004650 increased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:15289434 731427 Rpl24 ribosomal protein L24 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15289434 731427 Rpl24 ribosomal protein L24 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15289434 731427 Rpl24 ribosomal protein L24 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19011615 731427 Rpl24 ribosomal protein L24 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10049578 731427 Rpl24 ribosomal protein L24 gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:10681427 731427 Rpl24 ribosomal protein L24 gene MP:0010717 optic nerve coloboma IAGP N RGD:5509061 20141003 MGI PMID:10681427 731427 Rpl24 ribosomal protein L24 gene MP:0010717 optic nerve coloboma IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20220721 MGI PMID:35013307 731427 Rpl24 ribosomal protein L24 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8589526 731427 Rpl24 ribosomal protein L24 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15289434 731427 Rpl24 ribosomal protein L24 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10049578 731427 Rpl24 ribosomal protein L24 gene MP:0012536 delayed optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:10049578 731427 Rpl24 ribosomal protein L24 gene MP:0012536 delayed optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:9331275 731427 Rpl24 ribosomal protein L24 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:10681427 731427 Rpl24 ribosomal protein L24 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:9331275 731428 Cacng4 calcium channel, voltage-dependent, gamma subunit 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15677329 731428 Cacng4 calcium channel, voltage-dependent, gamma subunit 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15677329 731428 Cacng4 calcium channel, voltage-dependent, gamma subunit 4 gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:15677329 731428 Cacng4 calcium channel, voltage-dependent, gamma subunit 4 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20240418 MGI PMID:17880894 731428 Cacng4 calcium channel, voltage-dependent, gamma subunit 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15677329 731428 Cacng4 calcium channel, voltage-dependent, gamma subunit 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15677329 731428 Cacng4 calcium channel, voltage-dependent, gamma subunit 4 gene MP:0014372 decreased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:17880894 731430 Itga6 integrin alpha 6 gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20141003 MGI PMID:8673141 731430 Itga6 integrin alpha 6 gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16873583 731430 Itga6 integrin alpha 6 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:24227711 731430 Itga6 integrin alpha 6 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:8673141 731430 Itga6 integrin alpha 6 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:24227711 731430 Itga6 integrin alpha 6 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9742403 731430 Itga6 integrin alpha 6 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:9763436 731430 Itga6 integrin alpha 6 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9763436 731430 Itga6 integrin alpha 6 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:24227711 731430 Itga6 integrin alpha 6 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:9742403 731430 Itga6 integrin alpha 6 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0003591 urethra atresia IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:19967723 731430 Itga6 integrin alpha 6 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0003826 abnormal Mullerian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16873583 731430 Itga6 integrin alpha 6 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9763436 731430 Itga6 integrin alpha 6 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:24227711 731430 Itga6 integrin alpha 6 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:24227711 731430 Itga6 integrin alpha 6 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19967723 731430 Itga6 integrin alpha 6 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9742403 731430 Itga6 integrin alpha 6 gene MP:0008442 disorganized cortical plate IAGP N RGD:5509061 20141003 MGI PMID:9742403 731430 Itga6 integrin alpha 6 gene MP:0008509 disorganized retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0009111 pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0009252 absent urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0009569 abnormal left lung morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0009570 abnormal right lung morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141003 MGI PMID:24227711 731430 Itga6 integrin alpha 6 gene MP:0010116 abnormal primitive urogenital sinus morphology IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:19967723 731430 Itga6 integrin alpha 6 gene MP:0011011 impaired lung lobe morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0011032 impaired branching involved in terminal bronchiole morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24227711 731430 Itga6 integrin alpha 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8673141 731430 Itga6 integrin alpha 6 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10433923 731430 Itga6 integrin alpha 6 gene MP:0011730 increased myelin sheath thickness IAGP N RGD:5509061 20141003 MGI PMID:24227711 731430 Itga6 integrin alpha 6 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20141003 MGI PMID:24227711 731430 Itga6 integrin alpha 6 gene MP:0011904 abnormal Schwann cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24227711 731430 Itga6 integrin alpha 6 gene MP:0020452 abnormal axon radial sorting IAGP N RGD:5509061 20170914 MGI PMID:24227711 731430 Itga6 integrin alpha 6 gene MP:0030956 abnormal neuronal precursor cell migration IAGP N RGD:5509061 20190725 MGI PMID:9742403 731432 Dmgdh dimethylglycine dehydrogenase precursor gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 731432 Dmgdh dimethylglycine dehydrogenase precursor gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 731432 Dmgdh dimethylglycine dehydrogenase precursor gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15947421 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23524300 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:12538437 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16107690 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:15598866 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20160421 MGI 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15947421 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15947421 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:15947421 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11732988 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11732988 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15618213 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:9687309 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:15947421 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0003572 abnormal uterus development IAGP N RGD:5509061 20141003 MGI PMID:15084483 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:10652195 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:9687309 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:10952938 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:15084483 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:10952938 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:10952938 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20160421 MGI 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:15364874 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:15680392 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20161027 MGI PMID:10952938 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0009014 prolonged proestrus IAGP N RGD:5509061 20141003 MGI PMID:10952938 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0009016 abnormal estrus IAGP N RGD:5509061 20141003 MGI PMID:10952938 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0009018 short estrus IAGP N RGD:5509061 20141003 MGI PMID:10952938 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0009021 absent estrus IAGP N RGD:5509061 20141003 MGI PMID:10952938 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15947421 731433 Timp1 tissue inhibitor of metalloproteinase 1 gene MP:0013400 abnormal endometrial gland development IAGP N RGD:5509061 20141218 MGI PMID:15084483 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0001260 increased body weight IEA N RGD:5509061 20181011 MGI 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:20616166 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:20616166 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:20616166 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:20616166 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0005556 abnormal renal filtration rate IAGP N RGD:5509061 20141003 MGI PMID:20616166 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0005582 increased renin activity IAGP N RGD:5509061 20141003 MGI PMID:20616166 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0005633 increased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20181011 MGI 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0008560 increased tumor necrosis factor secretion IEA N RGD:5509061 20181011 MGI 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0011435 increased urine magnesium level IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0011447 abnormal renal glucose reabsorption IAGP N RGD:5509061 20141003 MGI PMID:20616166 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0011466 increased urine urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0011470 increased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0011923 abnormal bladder urine volume IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:20616166 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:23149623 731435 Slc5a2 solute carrier family 5 (sodium/glucose cotransporter), member 2 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:20616166 731436 Cd52 CD52 antigen gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18782223 731439 Rbm45 RNA binding motif protein 45 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220519 MGI 731439 Rbm45 RNA binding motif protein 45 gene MP:0000562 polydactyly IEA N RGD:5509061 20210826 MGI 731439 Rbm45 RNA binding motif protein 45 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210826 MGI 731439 Rbm45 RNA binding motif protein 45 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210826 MGI 731439 Rbm45 RNA binding motif protein 45 gene MP:0001785 edema IEA N RGD:5509061 20210826 MGI 731439 Rbm45 RNA binding motif protein 45 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210826 MGI 731439 Rbm45 RNA binding motif protein 45 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20210826 MGI 731439 Rbm45 RNA binding motif protein 45 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20210826 MGI 731439 Rbm45 RNA binding motif protein 45 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20210826 MGI 731439 Rbm45 RNA binding motif protein 45 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220519 MGI 731439 Rbm45 RNA binding motif protein 45 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220519 MGI 731439 Rbm45 RNA binding motif protein 45 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 731439 Rbm45 RNA binding motif protein 45 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20220519 MGI 731441 Polr2m polymerase (RNA) II (DNA directed) polypeptide M gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210422 MGI PMID:32381628 731441 Polr2m polymerase (RNA) II (DNA directed) polypeptide M gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20210422 MGI PMID:32381628 731441 Polr2m polymerase (RNA) II (DNA directed) polypeptide M gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20210422 MGI PMID:32381628 731441 Polr2m polymerase (RNA) II (DNA directed) polypeptide M gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20210422 MGI PMID:32381628 731441 Polr2m polymerase (RNA) II (DNA directed) polypeptide M gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20210422 MGI PMID:32381628 731441 Polr2m polymerase (RNA) II (DNA directed) polypeptide M gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20210422 MGI PMID:32381628 731441 Polr2m polymerase (RNA) II (DNA directed) polypeptide M gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20210422 MGI PMID:32381628 731441 Polr2m polymerase (RNA) II (DNA directed) polypeptide M gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20210422 MGI PMID:32381628 731441 Polr2m polymerase (RNA) II (DNA directed) polypeptide M gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20210422 MGI PMID:32381628 731441 Polr2m polymerase (RNA) II (DNA directed) polypeptide M gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20210422 MGI PMID:32381628 731442 Casp12 caspase 12 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17394578 731442 Casp12 caspase 12 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 731442 Casp12 caspase 12 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16625199 731442 Casp12 caspase 12 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:17394578 731442 Casp12 caspase 12 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17394578 731442 Casp12 caspase 12 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:10638761 731442 Casp12 caspase 12 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16625199 731442 Casp12 caspase 12 gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:16625199 731442 Casp12 caspase 12 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:16625199 731442 Casp12 caspase 12 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16625199 731442 Casp12 caspase 12 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:10638761 731442 Casp12 caspase 12 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16625199 731443 Dao D-amino acid oxidase gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20160304 MGI PMID:22837388 731443 Dao D-amino acid oxidase gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15694926 731443 Dao D-amino acid oxidase gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:15694926 731443 Dao D-amino acid oxidase gene MP:0002204 abnormal synaptic neurotransmitter level IAGP N RGD:5509061 20141003 MGI PMID:8100053 731443 Dao D-amino acid oxidase gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15694926 731443 Dao D-amino acid oxidase gene MP:0030639 decreased circulating taurine level IAGP N RGD:5509061 20180913 MGI PMID:8100053 731443 Dao D-amino acid oxidase gene MP:0030656 decreased circulating glycine level IAGP N RGD:5509061 20180913 MGI PMID:8100053 731443 Dao D-amino acid oxidase gene MP:0030659 decreased glycine level IAGP N RGD:5509061 20180913 MGI PMID:8100053 731443 Dao D-amino acid oxidase gene MP:0030673 increased circulating alanine level IAGP N RGD:5509061 20180913 MGI PMID:8100053 731443 Dao D-amino acid oxidase gene MP:0030691 increased serine level IAGP N RGD:5509061 20180920 MGI PMID:22837388 731443 Dao D-amino acid oxidase gene MP:0030694 increased circulating serine level IAGP N RGD:5509061 20180920 MGI PMID:22837388 731443 Dao D-amino acid oxidase gene MP:0030694 increased circulating serine level IAGP N RGD:5509061 20180927 MGI PMID:8100053 731443 Dao D-amino acid oxidase gene MP:0030706 increased glutamine level IAGP N RGD:5509061 20180927 MGI PMID:8100053 731443 Dao D-amino acid oxidase gene MP:0030736 increased glutamic acid level IAGP N RGD:5509061 20180927 MGI PMID:8100053 731443 Dao D-amino acid oxidase gene MP:0030740 decreased circulating glutamic acid level IAGP N RGD:5509061 20180927 MGI PMID:8100053 731445 Akap8 A kinase anchor protein 8 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:16751186 731445 Akap8 A kinase anchor protein 8 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16751186 731445 Akap8 A kinase anchor protein 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16751186 731445 Akap8 A kinase anchor protein 8 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16751186 731445 Akap8 A kinase anchor protein 8 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16751186 731445 Akap8 A kinase anchor protein 8 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16751186 731447 Hs3st1 heparan sulfate (glucosamine) 3-O-sulfotransferase 1 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:12671048 731447 Hs3st1 heparan sulfate (glucosamine) 3-O-sulfotransferase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12671048 731450 Lyst lysosomal trafficking regulator gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:13943454 731450 Lyst lysosomal trafficking regulator gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:16518687 731450 Lyst lysosomal trafficking regulator gene MP:0000371 diluted coat color IAGP N RGD:5509061 20200116 MGI PMID:25917818 731450 Lyst lysosomal trafficking regulator gene MP:0000372 irregular coat pigmentation IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20141003 MGI PMID:16518687 731450 Lyst lysosomal trafficking regulator gene MP:0000423 delayed hair regrowth IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0000427 abnormal hair cycle IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:4643821 731450 Lyst lysosomal trafficking regulator gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:4643821 731450 Lyst lysosomal trafficking regulator gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0000745 tremors IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0000858 abnormal metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:8605727 731450 Lyst lysosomal trafficking regulator gene MP:0000880 decreased Purkinje cell number IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:1523694 731450 Lyst lysosomal trafficking regulator gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:2806196 731450 Lyst lysosomal trafficking regulator gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:15743322 731450 Lyst lysosomal trafficking regulator gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:15743322 731450 Lyst lysosomal trafficking regulator gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16518687 731450 Lyst lysosomal trafficking regulator gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:4643821 731450 Lyst lysosomal trafficking regulator gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:8605727 731450 Lyst lysosomal trafficking regulator gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:19029039 731450 Lyst lysosomal trafficking regulator gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:13943454 731450 Lyst lysosomal trafficking regulator gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0001522 impaired swimming IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0001525 impaired balance IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0001760 abnormal urine enzyme level IAGP N RGD:5509061 20141003 MGI PMID:408 731450 Lyst lysosomal trafficking regulator gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:3965401 731450 Lyst lysosomal trafficking regulator gene MP:0001798 impaired macrophage phagocytosis IEA N RGD:5509061 20150305 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:4643821 731450 Lyst lysosomal trafficking regulator gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:4643821 731450 Lyst lysosomal trafficking regulator gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:2806196 731450 Lyst lysosomal trafficking regulator gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:7366734 731450 Lyst lysosomal trafficking regulator gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:16518687 731450 Lyst lysosomal trafficking regulator gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0002095 abnormal skin pigmentation IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:7366733 731450 Lyst lysosomal trafficking regulator gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15743322 731450 Lyst lysosomal trafficking regulator gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:4643821 731450 Lyst lysosomal trafficking regulator gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:8320959 731450 Lyst lysosomal trafficking regulator gene MP:0002412 increased susceptibility to bacterial infection IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:5590154 731450 Lyst lysosomal trafficking regulator gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:1523694 731450 Lyst lysosomal trafficking regulator gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:1523694 731450 Lyst lysosomal trafficking regulator gene MP:0002763 ectopic Bergmann glia cells IAGP N RGD:5509061 20141003 MGI PMID:1523694 731450 Lyst lysosomal trafficking regulator gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16518687 731450 Lyst lysosomal trafficking regulator gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:5590154 731450 Lyst lysosomal trafficking regulator gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:7089489 731450 Lyst lysosomal trafficking regulator gene MP:0003173 decreased lysosomal enzyme secretion IAGP N RGD:5509061 20141003 MGI PMID:408 731450 Lyst lysosomal trafficking regulator gene MP:0003173 decreased lysosomal enzyme secretion IAGP N RGD:5509061 20141003 MGI PMID:6696991 731450 Lyst lysosomal trafficking regulator gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16518687 731450 Lyst lysosomal trafficking regulator gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:408 731450 Lyst lysosomal trafficking regulator gene MP:0004221 abnormal iridocorneal angle IAGP N RGD:5509061 20141003 MGI PMID:19029039 731450 Lyst lysosomal trafficking regulator gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16518687 731450 Lyst lysosomal trafficking regulator gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20141003 MGI PMID:6696991 731450 Lyst lysosomal trafficking regulator gene MP:0004844 abnormal vestibuloocular reflex IAGP N RGD:5509061 20141003 MGI PMID:3584547 731450 Lyst lysosomal trafficking regulator gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:6218091 731450 Lyst lysosomal trafficking regulator gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:1113502 731450 Lyst lysosomal trafficking regulator gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:4697831 731450 Lyst lysosomal trafficking regulator gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:6170520 731450 Lyst lysosomal trafficking regulator gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20141003 MGI PMID:408 731450 Lyst lysosomal trafficking regulator gene MP:0005060 accumulation of giant lysosomes in kidney/renal tubule cells IAGP N RGD:5509061 20141003 MGI PMID:408 731450 Lyst lysosomal trafficking regulator gene MP:0005061 abnormal eosinophil morphology IAGP N RGD:5509061 20141003 MGI PMID:5590154 731450 Lyst lysosomal trafficking regulator gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:5590154 731450 Lyst lysosomal trafficking regulator gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:489978 731450 Lyst lysosomal trafficking regulator gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:7366734 731450 Lyst lysosomal trafficking regulator gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0005071 enlarged hair follicle melanin granules IAGP N RGD:5509061 20141003 MGI PMID:16518687 731450 Lyst lysosomal trafficking regulator gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:16518687 731450 Lyst lysosomal trafficking regulator gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 731450 Lyst lysosomal trafficking regulator gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:4697831 731450 Lyst lysosomal trafficking regulator gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:5590154 731450 Lyst lysosomal trafficking regulator gene MP:0005077 abnormal melanogenesis IAGP N RGD:5509061 20141003 MGI PMID:4634048 731450 Lyst lysosomal trafficking regulator gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:6977094 731450 Lyst lysosomal trafficking regulator gene MP:0005100 abnormal choroid pigmentation IAGP N RGD:5509061 20141003 MGI PMID:13943454 731450 Lyst lysosomal trafficking regulator gene MP:0005101 abnormal ciliary body pigmentation IAGP N RGD:5509061 20141003 MGI PMID:13943454 731450 Lyst lysosomal trafficking regulator gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:13943454 731450 Lyst lysosomal trafficking regulator gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16518687 731450 Lyst lysosomal trafficking regulator gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18715234 731450 Lyst lysosomal trafficking regulator gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:19029039 731450 Lyst lysosomal trafficking regulator gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:13943454 731450 Lyst lysosomal trafficking regulator gene MP:0005114 premature hair loss IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:13943454 731450 Lyst lysosomal trafficking regulator gene MP:0005194 abnormal anterior uvea morphology IAGP N RGD:5509061 20141003 MGI PMID:19029039 731450 Lyst lysosomal trafficking regulator gene MP:0005199 abnormal iris pigment epithelium IAGP N RGD:5509061 20141003 MGI PMID:16518687 731450 Lyst lysosomal trafficking regulator gene MP:0005199 abnormal iris pigment epithelium IAGP N RGD:5509061 20141003 MGI PMID:19029039 731450 Lyst lysosomal trafficking regulator gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16518687 731450 Lyst lysosomal trafficking regulator gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:19029039 731450 Lyst lysosomal trafficking regulator gene MP:0005208 abnormal iris stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:19029039 731450 Lyst lysosomal trafficking regulator gene MP:0005398 decreased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:3965401 731450 Lyst lysosomal trafficking regulator gene MP:0005408 hypopigmentation IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:6696991 731450 Lyst lysosomal trafficking regulator gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:2806196 731450 Lyst lysosomal trafficking regulator gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15743322 731450 Lyst lysosomal trafficking regulator gene MP:0008020 abnormal dermal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16518687 731450 Lyst lysosomal trafficking regulator gene MP:0008041 absent NK T cells IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:1523694 731450 Lyst lysosomal trafficking regulator gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0009273 abnormal hair shaft melanin granule shape IAGP N RGD:5509061 20141003 MGI PMID:5590154 731450 Lyst lysosomal trafficking regulator gene MP:0009379 abnormal foot pigmentation IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0009434 paraparesis IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20141003 MGI PMID:6696991 731450 Lyst lysosomal trafficking regulator gene MP:0009557 decreased platelet ADP level IAGP N RGD:5509061 20141003 MGI PMID:6696991 731450 Lyst lysosomal trafficking regulator gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:2513223 731450 Lyst lysosomal trafficking regulator gene MP:0010011 ectopic hippocampus pyramidal cells IAGP N RGD:5509061 20141003 MGI PMID:1523694 731450 Lyst lysosomal trafficking regulator gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0010192 abnormal retina melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 731450 Lyst lysosomal trafficking regulator gene MP:0010193 abnormal choroid melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 731450 Lyst lysosomal trafficking regulator gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7089489 731450 Lyst lysosomal trafficking regulator gene MP:0010815 enlarged alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:15743322 731450 Lyst lysosomal trafficking regulator gene MP:0010922 alveolitis IAGP N RGD:5509061 20141003 MGI PMID:15743322 731450 Lyst lysosomal trafficking regulator gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0011277 decreased tail pigmentation IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0011279 decreased ear pigmentation IEA N RGD:5509061 20111116 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:4643821 731450 Lyst lysosomal trafficking regulator gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0014130 thymus cyst IAGP N RGD:5509061 20160324 MGI PMID:8806787 731450 Lyst lysosomal trafficking regulator gene MP:0020916 increased susceptibility to Herpesvirales infection IEA N RGD:5509061 20200430 MGI 731450 Lyst lysosomal trafficking regulator gene MP:0030917 enlarged melanosome IAGP N RGD:5509061 20181227 MGI PMID:4697831 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:24168030 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:11927540 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:12413896 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11927540 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11927540 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:24168030 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11927540 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:12413896 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:11927540 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:11927540 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11927540 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:11927540 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:24168030 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0009593 absent chorion IAGP N RGD:5509061 20141003 MGI PMID:11927540 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11927540 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12413896 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24168030 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11927540 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:24168030 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11927540 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0011201 abnormal visceral yolk sac cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:11927540 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0011208 small proamniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:11927540 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:12413896 731452 Dab2 disabled 2, mitogen-responsive phosphoprotein gene MP:0012159 absent anterior visceral endoderm IAGP N RGD:5509061 20141003 MGI PMID:11927540 731454 Myo5a myosin VA gene MP:0000015 abnormal ear pigmentation IEA N RGD:5509061 20111116 MGI 731454 Myo5a myosin VA gene MP:0000243 myoclonus IEA N RGD:5509061 20111116 MGI 731454 Myo5a myosin VA gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:13943454 731454 Myo5a myosin VA gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:17247308 731454 Myo5a myosin VA gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:21508232 731454 Myo5a myosin VA gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:23349704 731454 Myo5a myosin VA gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:2379821 731454 Myo5a myosin VA gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:3141922 731454 Myo5a myosin VA gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:9560409 731454 Myo5a myosin VA gene MP:0000371 diluted coat color IAGP N RGD:5509061 20190124 MGI PMID:25340873 731454 Myo5a myosin VA gene MP:0000371 diluted coat color IAGP N RGD:5509061 20200220 MGI PMID:18902556 731454 Myo5a myosin VA gene MP:0000423 delayed hair regrowth IEA N RGD:5509061 20111116 MGI 731454 Myo5a myosin VA gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20190124 MGI PMID:25340873 731454 Myo5a myosin VA gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10749990 731454 Myo5a myosin VA gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:21508232 731454 Myo5a myosin VA gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:10749990 731454 Myo5a myosin VA gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 731454 Myo5a myosin VA gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17247308 731454 Myo5a myosin VA gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:2379821 731454 Myo5a myosin VA gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10749990 731454 Myo5a myosin VA gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21508232 731454 Myo5a myosin VA gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22258617 731454 Myo5a myosin VA gene MP:0001394 circling IEA N RGD:5509061 20150101 MGI 731454 Myo5a myosin VA gene MP:0001399 hyperactivity IEA N RGD:5509061 20160804 MGI 731454 Myo5a myosin VA gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10749990 731454 Myo5a myosin VA gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21508232 731454 Myo5a myosin VA gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21508232 731454 Myo5a myosin VA gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:21508232 731454 Myo5a myosin VA gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10749990 731454 Myo5a myosin VA gene MP:0001524 impaired limb coordination IEA N RGD:5509061 20111116 MGI 731454 Myo5a myosin VA gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:10749990 731454 Myo5a myosin VA gene MP:0002064 seizures IEA N RGD:5509061 20111116 MGI 731454 Myo5a myosin VA gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:10749990 731454 Myo5a myosin VA gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:3141922 731454 Myo5a myosin VA gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:9560409 731454 Myo5a myosin VA gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17247308 731454 Myo5a myosin VA gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:3141922 731454 Myo5a myosin VA gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:3422417 731454 Myo5a myosin VA gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9560409 731454 Myo5a myosin VA gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20150709 MGI PMID:24721909 731454 Myo5a myosin VA gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20190124 MGI PMID:25340873 731454 Myo5a myosin VA gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:3141922 731454 Myo5a myosin VA gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9560409 731454 Myo5a myosin VA gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20120112 MGI 731454 Myo5a myosin VA gene MP:0002807 abnormal eye blink conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21508232 731454 Myo5a myosin VA gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17247639 731454 Myo5a myosin VA gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:6886377 731454 Myo5a myosin VA gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8962090 731454 Myo5a myosin VA gene MP:0002880 opisthotonus IAGP N RGD:5509061 20141003 MGI PMID:10749990 731454 Myo5a myosin VA gene MP:0002880 opisthotonus IAGP N RGD:5509061 20141003 MGI PMID:12644183 731454 Myo5a myosin VA gene MP:0002880 opisthotonus IAGP N RGD:5509061 20141003 MGI PMID:3141922 731454 Myo5a myosin VA gene MP:0003171 phenotypic reversion IAGP N RGD:5509061 20141003 MGI PMID:6305507 731454 Myo5a myosin VA gene MP:0003176 reversion by viral sequence excision IAGP N RGD:5509061 20141003 MGI PMID:6305507 731454 Myo5a myosin VA gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:21508232 731454 Myo5a myosin VA gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:3141922 731454 Myo5a myosin VA gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:17247308 731454 Myo5a myosin VA gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:21508232 731454 Myo5a myosin VA gene MP:0004263 abnormal limb posture IEA N RGD:5509061 20111116 MGI 731454 Myo5a myosin VA gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 731454 Myo5a myosin VA gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 731454 Myo5a myosin VA gene MP:0005072 abnormal hair follicle melanin granule morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 731454 Myo5a myosin VA gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 731454 Myo5a myosin VA gene MP:0005114 premature hair loss IEA N RGD:5509061 20111116 MGI 731454 Myo5a myosin VA gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20200220 MGI PMID:18902556 731454 Myo5a myosin VA gene MP:0005174 abnormal tail pigmentation IEA N RGD:5509061 20111116 MGI 731454 Myo5a myosin VA gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:23349704 731454 Myo5a myosin VA gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21508232 731454 Myo5a myosin VA gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:10749990 731454 Myo5a myosin VA gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:21508232 731454 Myo5a myosin VA gene MP:0008733 abnormal hair shaft melanin granule distribution IAGP N RGD:5509061 20141003 MGI PMID:17247308 731454 Myo5a myosin VA gene MP:0009379 abnormal foot pigmentation IEA N RGD:5509061 20111116 MGI 731454 Myo5a myosin VA gene MP:0009387 abnormal epidermal pigmentation IAGP N RGD:5509061 20150709 MGI PMID:24721909 731454 Myo5a myosin VA gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20150709 MGI PMID:24721909 731454 Myo5a myosin VA gene MP:0009555 abnormal hair follicle melanin granule distribution IAGP N RGD:5509061 20141003 MGI PMID:4634048 731454 Myo5a myosin VA gene MP:0010193 abnormal choroid melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:4634048 731454 Myo5a myosin VA gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:12644183 731454 Myo5a myosin VA gene MP:0011083 lethality at weaning, complete penetrance IEA N RGD:5509061 20111116 MGI 731454 Myo5a myosin VA gene MP:0011085 postnatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 731454 Myo5a myosin VA gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 731454 Myo5a myosin VA gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23349704 731456 Scpep1 serine carboxypeptidase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19187242 731456 Scpep1 serine carboxypeptidase 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:19574551 731458 Fgf20 fibroblast growth factor 20 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:22235191 731458 Fgf20 fibroblast growth factor 20 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0000274 enlarged heart IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20151217 MGI PMID:23431057 731458 Fgf20 fibroblast growth factor 20 gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20151217 MGI PMID:23431057 731458 Fgf20 fibroblast growth factor 20 gene MP:0000405 abnormal auchene hair morphology IAGP N RGD:5509061 20151217 MGI PMID:23431057 731458 Fgf20 fibroblast growth factor 20 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0001314 cornea opacity IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:22235191 731458 Fgf20 fibroblast growth factor 20 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22235191 731458 Fgf20 fibroblast growth factor 20 gene MP:0002989 small kidney IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20151217 MGI PMID:23431057 731458 Fgf20 fibroblast growth factor 20 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22235191 731458 Fgf20 fibroblast growth factor 20 gene MP:0003883 enlarged stomach IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0003918 decreased kidney weight IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22235191 731458 Fgf20 fibroblast growth factor 20 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:22235191 731458 Fgf20 fibroblast growth factor 20 gene MP:0004408 decreased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:22235191 731458 Fgf20 fibroblast growth factor 20 gene MP:0004497 decreased organ of Corti supporting cell number IAGP N RGD:5509061 20141003 MGI PMID:22235191 731458 Fgf20 fibroblast growth factor 20 gene MP:0004589 abnormal cochlear hair cell development IAGP N RGD:5509061 20141003 MGI PMID:22235191 731458 Fgf20 fibroblast growth factor 20 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0006365 absent guard hair IAGP N RGD:5509061 20151217 MGI PMID:23431057 731458 Fgf20 fibroblast growth factor 20 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0010099 abnormal thoracic cage shape IEA N RGD:5509061 20240523 MGI 731458 Fgf20 fibroblast growth factor 20 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:22235191 731459 Acox2 acyl-Coenzyme A oxidase 2, branched chain gene MP:0001860 liver inflammation IAGP N RGD:5509061 20220505 MGI PMID:35351852 731459 Acox2 acyl-Coenzyme A oxidase 2, branched chain gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20220505 MGI PMID:35351852 731459 Acox2 acyl-Coenzyme A oxidase 2, branched chain gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20220505 MGI PMID:35351852 731460 Casp2 caspase 2 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20230119 MGI 731460 Casp2 caspase 2 gene MP:0000909 abnormal facial motor nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9573047 731460 Casp2 caspase 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:15210727 731460 Casp2 caspase 2 gene MP:0001025 abnormal sympathetic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9573047 731460 Casp2 caspase 2 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9573047 731460 Casp2 caspase 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 731460 Casp2 caspase 2 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 731460 Casp2 caspase 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 731460 Casp2 caspase 2 gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 731460 Casp2 caspase 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 731460 Casp2 caspase 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20231207 MGI 731460 Casp2 caspase 2 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9573047 731460 Casp2 caspase 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 731460 Casp2 caspase 2 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15210727 731460 Casp2 caspase 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 731460 Casp2 caspase 2 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230119 MGI 731460 Casp2 caspase 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15210727 731460 Casp2 caspase 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 731460 Casp2 caspase 2 gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 731460 Casp2 caspase 2 gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9573047 731460 Casp2 caspase 2 gene MP:0005238 increased brain size IEA N RGD:5509061 20230119 MGI 731460 Casp2 caspase 2 gene MP:0006361 abnormal female germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9573047 731460 Casp2 caspase 2 gene MP:0008781 abnormal B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9573047 731460 Casp2 caspase 2 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20230119 MGI 731460 Casp2 caspase 2 gene MP:0011120 increased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:9573047 731462 Mas1 MAS1 oncogene gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:9565612 731462 Mas1 MAS1 oncogene gene MP:0002764 short tibia IEA N RGD:5509061 20201022 MGI 731462 Mas1 MAS1 oncogene gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:19262461 731462 Mas1 MAS1 oncogene gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:19262461 731462 Mas1 MAS1 oncogene gene MP:0002959 increased urine microalbumin level IAGP N RGD:5509061 20141003 MGI PMID:19262461 731462 Mas1 MAS1 oncogene gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:9565612 731462 Mas1 MAS1 oncogene gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19262461 731462 Mas1 MAS1 oncogene gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 731462 Mas1 MAS1 oncogene gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:19262461 731462 Mas1 MAS1 oncogene gene MP:0005526 decreased renal plasma flow rate IAGP N RGD:5509061 20141003 MGI PMID:19262461 731462 Mas1 MAS1 oncogene gene MP:0005527 increased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:19262461 731462 Mas1 MAS1 oncogene gene MP:0005531 increased renal vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:19262461 731462 Mas1 MAS1 oncogene gene MP:0005557 increased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:19262461 731462 Mas1 MAS1 oncogene gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:19262461 731462 Mas1 MAS1 oncogene gene MP:0008055 increased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:19262461 731462 Mas1 MAS1 oncogene gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 731462 Mas1 MAS1 oncogene gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19262461 731462 Mas1 MAS1 oncogene gene MP:0011432 decreased urine flow rate IAGP N RGD:5509061 20141003 MGI PMID:19262461 731466 Ubqln1 ubiquilin 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:24553923 731466 Ubqln1 ubiquilin 1 gene MP:0003075 abnormal response to CNS ischemic injury IAGP N RGD:5509061 20141003 MGI PMID:24553923 731466 Ubqln1 ubiquilin 1 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:24553923 731469 Stx4a syntaxin 4A (placental) gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11375421 731469 Stx4a syntaxin 4A (placental) gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11375421 731469 Stx4a syntaxin 4A (placental) gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11375421 731469 Stx4a syntaxin 4A (placental) gene MP:0005387 immune system phenotype IAGP N RGD:5509061 20230518 MGI PMID:30563839 731469 Stx4a syntaxin 4A (placental) gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230518 MGI PMID:30563839 731469 Stx4a syntaxin 4A (placental) gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11375421 731469 Stx4a syntaxin 4A (placental) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 731472 Mbl2 mannose-binding lectin (protein C) 2 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15148336 731472 Mbl2 mannose-binding lectin (protein C) 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:15148336 731472 Mbl2 mannose-binding lectin (protein C) 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:15749852 731472 Mbl2 mannose-binding lectin (protein C) 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15148336 731472 Mbl2 mannose-binding lectin (protein C) 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16424207 731472 Mbl2 mannose-binding lectin (protein C) 2 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:15749852 731472 Mbl2 mannose-binding lectin (protein C) 2 gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:15882434 731472 Mbl2 mannose-binding lectin (protein C) 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:15148336 731472 Mbl2 mannose-binding lectin (protein C) 2 gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:15882434 731472 Mbl2 mannose-binding lectin (protein C) 2 gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:15749852 731472 Mbl2 mannose-binding lectin (protein C) 2 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:15498041 731472 Mbl2 mannose-binding lectin (protein C) 2 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:15749852 731472 Mbl2 mannose-binding lectin (protein C) 2 gene MP:0008552 abnormal circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15148336 731472 Mbl2 mannose-binding lectin (protein C) 2 gene MP:0008595 abnormal circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:15148336 731473 Fbp1 fructose bisphosphatase 1 gene MP:0000189 hypoglycemia IEA N RGD:5509061 20190110 MGI 731474 Hmgcs1 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20240523 MGI 731474 Hmgcs1 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 731474 Hmgcs1 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16683252 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16683252 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16683252 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16683252 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16683252 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:23922840 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16683252 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:16683252 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0001987 alcohol preference IAGP N RGD:5509061 20141003 MGI PMID:16683252 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12451126 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:23922840 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20141003 MGI PMID:16683252 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0002635 reduced sensorimotor gating IAGP N RGD:5509061 20141003 MGI PMID:23922840 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:16683252 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0002850 saccharin preference IAGP N RGD:5509061 20141003 MGI PMID:16683252 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12815026 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0003444 abnormal neurotransmitter uptake IAGP N RGD:5509061 20141003 MGI PMID:12815026 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:23922840 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:16683252 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:23922840 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0004210 abnormal bitter taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16683252 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:12815026 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0006299 abnormal latent inhibition of conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23922840 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:23922840 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:23922840 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16683252 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23922840 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:23922840 731476 Slc6a1 solute carrier family 6 (neurotransmitter transporter, GABA), member 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:23922840 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10932232 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:7675081 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:9334720 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:10606624 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:11413087 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10606624 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10932232 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:10606624 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11413087 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:10932232 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:10932232 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:9334720 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10606624 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10899071 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11788366 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:14664706 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:7675081 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9334720 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7675081 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:9334720 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10606624 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11217863 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11394912 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11435467 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9312184 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11435467 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14664706 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:7675081 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9312184 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9334720 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7675081 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:10932232 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:7675081 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10932232 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11435467 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:9334720 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:7675081 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15562255 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:10606624 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:14664706 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:7675081 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:9334720 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11788366 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:10899071 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:14664706 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15562255 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15562255 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:7675081 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:10606624 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:11788366 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:11413087 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:11788366 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:10932232 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:10606624 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:10932232 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11217863 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15562255 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10932232 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10606624 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:10932232 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11217863 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:7675081 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:9312184 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:9334720 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11217863 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9312184 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15562255 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11435467 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:14664706 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15562255 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10899071 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:14664706 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:9334720 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:11788366 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:9334720 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:7675081 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:11788366 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:7675081 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20191226 MGI PMID:11788366 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:10932232 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0013759 decreased intestinal glucose absorption IAGP N RGD:5509061 20191031 MGI PMID:11435467 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20191226 MGI PMID:11413087 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:11435467 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:14664706 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:11435467 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:14664706 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:11413087 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:14664706 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0030020 decreased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:10606624 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0030020 decreased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:11413087 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0030022 decreased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:11435467 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0030022 decreased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:9312184 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:9334720 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:10932232 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:11435467 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:14664706 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:9334720 731479 Slc2a4 solute carrier family 2 (facilitated glucose transporter), member 4 gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:14664706 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0001523 impaired righting response IAGP N RGD:5509061 20231207 MGI PMID:37782669 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:16022389 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20231207 MGI PMID:37782669 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20231207 MGI PMID:37782669 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16022389 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0002194 maximal tonic hindlimb extension seizures IAGP N RGD:5509061 20231207 MGI PMID:37782669 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16022389 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20231207 MGI PMID:37782669 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0005356 positive geotaxis IAGP N RGD:5509061 20231207 MGI PMID:37782669 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:16022389 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20231207 MGI PMID:37782669 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20231207 MGI PMID:37782669 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16022389 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20231207 MGI PMID:37782669 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0020419 decreased cardiac muscle relaxation IAGP N RGD:5509061 20170406 MGI PMID:26039991 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0021165 behavioral developmental delay IAGP N RGD:5509061 20231207 MGI PMID:37782669 731483 Hnrnpu heterogeneous nuclear ribonucleoprotein U gene MP:0030567 abnormal I band morphology IAGP N RGD:5509061 20180531 MGI PMID:26039991 731486 Sh3bp4 SH3-domain binding protein 4 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:23064365 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:15372110 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:15372110 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15372110 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23064365 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:12486099 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23064365 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23064365 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0005025 abnormal response to infection IEA N RGD:5509061 20111116 MGI 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:23064365 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IEA N RGD:5509061 20111116 MGI 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15372110 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12486099 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12486099 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15372110 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:15372110 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008556 abnormal tumor necrosis factor secretion IEA N RGD:5509061 20111116 MGI 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:11163183 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22733995 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23064365 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008563 decreased interferon-alpha secretion IEA N RGD:5509061 20111116 MGI 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008565 decreased interferon-beta secretion IEA N RGD:5509061 20111116 MGI 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008648 decreased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:22733995 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008658 decreased interleukin-1 beta secretion IEA N RGD:5509061 20111116 MGI 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008669 increased interleukin-12b secretion IEA N RGD:5509061 20111116 MGI 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:22733995 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008706 decreased interleukin-6 secretion IEA N RGD:5509061 20111116 MGI 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:11163183 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23064365 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23064365 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23064365 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23064365 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:23064365 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0011079 decreased macrophage cytokine production IEA N RGD:5509061 20151015 MGI 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:23064365 731489 Map3k8 mitogen-activated protein kinase kinase kinase 8 gene MP:0014234 decreased enterocyte apoptosis IAGP N RGD:5509061 20230323 MGI PMID:23064365 731493 Cdc25a cell division cycle 25A gene MP:0000130 abnormal trabecular bone morphology IEA N RGD:5509061 20111116 MGI 731493 Cdc25a cell division cycle 25A gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12411323 731493 Cdc25a cell division cycle 25A gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12411323 731493 Cdc25a cell division cycle 25A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17638870 731493 Cdc25a cell division cycle 25A gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21283624 731493 Cdc25a cell division cycle 25A gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21283624 731493 Cdc25a cell division cycle 25A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21283624 731493 Cdc25a cell division cycle 25A gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19273838 731493 Cdc25a cell division cycle 25A gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:18936171 731493 Cdc25a cell division cycle 25A gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:17638870 731493 Cdc25a cell division cycle 25A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19273838 731493 Cdc25a cell division cycle 25A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19273838 731493 Cdc25a cell division cycle 25A gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:19273838 731493 Cdc25a cell division cycle 25A gene MP:0003693 abnormal blastocyst hatching IAGP N RGD:5509061 20141003 MGI PMID:17638870 731493 Cdc25a cell division cycle 25A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19273838 731493 Cdc25a cell division cycle 25A gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:18936171 731493 Cdc25a cell division cycle 25A gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:12411323 731493 Cdc25a cell division cycle 25A gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:18936171 731493 Cdc25a cell division cycle 25A gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:18936171 731493 Cdc25a cell division cycle 25A gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:19273838 731493 Cdc25a cell division cycle 25A gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:21283624 731493 Cdc25a cell division cycle 25A gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:12411323 731493 Cdc25a cell division cycle 25A gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19273838 731493 Cdc25a cell division cycle 25A gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:19273838 731493 Cdc25a cell division cycle 25A gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20141003 MGI PMID:21283624 731493 Cdc25a cell division cycle 25A gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21283624 731493 Cdc25a cell division cycle 25A gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21283624 731493 Cdc25a cell division cycle 25A gene MP:0010159 abnormal enterocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:21283624 731493 Cdc25a cell division cycle 25A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21283624 731493 Cdc25a cell division cycle 25A gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17638870 731493 Cdc25a cell division cycle 25A gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19273838 731493 Cdc25a cell division cycle 25A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 731493 Cdc25a cell division cycle 25A gene MP:0013958 decreased small intestine length IAGP N RGD:5509061 20160310 MGI PMID:19273838 731493 Cdc25a cell division cycle 25A gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20160310 MGI PMID:19273838 731493 Cdc25a cell division cycle 25A gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:18936171 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20180201 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0005161 hematuria IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11805078 731496 Mgat2 mannoside acetylglucosaminyltransferase 2 gene MP:0012359 increased partial thromboplastin time IAGP N RGD:5509061 20201001 MGI PMID:11805078 731498 Prdx4 peroxiredoxin 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19105792 731498 Prdx4 peroxiredoxin 4 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:19105792 731498 Prdx4 peroxiredoxin 4 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:19105792 731498 Prdx4 peroxiredoxin 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19105792 731498 Prdx4 peroxiredoxin 4 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:19105792 731499 Setd4 SET domain containing 4 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20210506 MGI PMID:31794893 731499 Setd4 SET domain containing 4 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20210506 MGI PMID:31794893 731499 Setd4 SET domain containing 4 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20210506 MGI PMID:31794893 731499 Setd4 SET domain containing 4 gene MP:0003010 decreased mortality induced by ionizing radiation IAGP N RGD:5509061 20210506 MGI PMID:31794893 731499 Setd4 SET domain containing 4 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20210506 MGI PMID:31794893 731499 Setd4 SET domain containing 4 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20210506 MGI PMID:31794893 731499 Setd4 SET domain containing 4 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 731499 Setd4 SET domain containing 4 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20210506 MGI PMID:31794893 731499 Setd4 SET domain containing 4 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20210506 MGI PMID:31794893 731499 Setd4 SET domain containing 4 gene MP:0010307 abnormal tumor latency IAGP N RGD:5509061 20210506 MGI PMID:31794893 731499 Setd4 SET domain containing 4 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20210506 MGI PMID:31794893 731499 Setd4 SET domain containing 4 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20210506 MGI PMID:31794893 731499 Setd4 SET domain containing 4 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20240516 MGI PMID:31376731 731499 Setd4 SET domain containing 4 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20181227 MGI 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20181227 MGI 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:22983607 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22983607 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20211021 MGI 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:22983607 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22983607 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20181227 MGI 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20210128 MGI 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20181227 MGI 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:22983607 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210128 MGI 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22983607 731501 Hipk3 homeodomain interacting protein kinase 3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 731506 Serpini1 serine (or cysteine) peptidase inhibitor, clade I, member 1 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12837630 731506 Serpini1 serine (or cysteine) peptidase inhibitor, clade I, member 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:12837630 731506 Serpini1 serine (or cysteine) peptidase inhibitor, clade I, member 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12837630 731506 Serpini1 serine (or cysteine) peptidase inhibitor, clade I, member 1 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:12837630 731508 Magt1 magnesium transporter 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 731508 Magt1 magnesium transporter 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20562862 731508 Magt1 magnesium transporter 1 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20180524 MGI PMID:29581357 731508 Magt1 magnesium transporter 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20180524 MGI PMID:29581357 731508 Magt1 magnesium transporter 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20180524 MGI PMID:29581357 731508 Magt1 magnesium transporter 1 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20180524 MGI PMID:29581357 731508 Magt1 magnesium transporter 1 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20180524 MGI PMID:29581357 731508 Magt1 magnesium transporter 1 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20180524 MGI PMID:29581357 731511 Tpm3 tropomyosin 3, gamma gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19005216 731511 Tpm3 tropomyosin 3, gamma gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19005216 731511 Tpm3 tropomyosin 3, gamma gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14993271 731512 F7 coagulation factor VII gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20160421 MGI 731512 F7 coagulation factor VII gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10021455 731512 F7 coagulation factor VII gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10749569 731512 F7 coagulation factor VII gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9384381 731512 F7 coagulation factor VII gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10749569 731512 F7 coagulation factor VII gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16268461 731512 F7 coagulation factor VII gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9384381 731512 F7 coagulation factor VII gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:10749569 731512 F7 coagulation factor VII gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:10021455 731512 F7 coagulation factor VII gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:10749569 731512 F7 coagulation factor VII gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:16268461 731512 F7 coagulation factor VII gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16268461 731512 F7 coagulation factor VII gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160421 MGI 731512 F7 coagulation factor VII gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:10749569 731512 F7 coagulation factor VII gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:16268461 731512 F7 coagulation factor VII gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20201001 MGI PMID:16268461 731512 F7 coagulation factor VII gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20160421 MGI 731512 F7 coagulation factor VII gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160421 MGI 731512 F7 coagulation factor VII gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10021455 731512 F7 coagulation factor VII gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10749569 731512 F7 coagulation factor VII gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9384381 731512 F7 coagulation factor VII gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 731512 F7 coagulation factor VII gene MP:0012356 increased prothrombin time IAGP N RGD:5509061 20201001 MGI PMID:16268461 731512 F7 coagulation factor VII gene MP:0012359 increased partial thromboplastin time IAGP N RGD:5509061 20201001 MGI PMID:16268461 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11430820 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:19181853 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220811 MGI 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220811 MGI 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:11430820 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210826 MGI 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20240926 MGI 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11430820 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19181853 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:11430820 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240926 MGI 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:19181853 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11430820 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19181853 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 731513 Eif2s1 eukaryotic translation initiation factor 2, subunit 1 alpha gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240926 MGI 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20241114 MGI PMID:35934110 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20241114 MGI PMID:35934110 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20241114 MGI PMID:35934110 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0002083 premature death IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0002138 abnormal hepatobiliary system morphology IAGP N RGD:5509061 20241114 MGI PMID:35934110 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20241114 MGI PMID:35934110 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20241114 MGI PMID:35934110 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20241114 MGI PMID:35934110 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20241114 MGI PMID:35934110 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20241114 MGI PMID:35934110 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20241114 MGI PMID:35934110 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20241114 MGI PMID:35934110 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20241114 MGI PMID:35934110 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0012338 decreased bile salt level IAGP N RGD:5509061 20240613 MGI PMID:31645370 731517 Cyp2c70 cytochrome P450, family 2, subfamily c, polypeptide 70 gene MP:0014479 decreased feces bile salt level IAGP N RGD:5509061 20240704 MGI PMID:31645370 731519 Gja4 gap junction protein, alpha 4 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:12435353 731519 Gja4 gap junction protein, alpha 4 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12435353 731519 Gja4 gap junction protein, alpha 4 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12435353 731519 Gja4 gap junction protein, alpha 4 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12435353 731519 Gja4 gap junction protein, alpha 4 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12435353 731519 Gja4 gap junction protein, alpha 4 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9020357 731519 Gja4 gap junction protein, alpha 4 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20220407 MGI PMID:9020357 731519 Gja4 gap junction protein, alpha 4 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:9020357 731519 Gja4 gap junction protein, alpha 4 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:12435353 731519 Gja4 gap junction protein, alpha 4 gene MP:0008869 anovulation IAGP N RGD:5509061 20220407 MGI PMID:9020357 731519 Gja4 gap junction protein, alpha 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12435353 731519 Gja4 gap junction protein, alpha 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12435353 731519 Gja4 gap junction protein, alpha 4 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12435353 731522 Rgs12 regulator of G-protein signaling 12 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:23349096 731522 Rgs12 regulator of G-protein signaling 12 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:23349096 731522 Rgs12 regulator of G-protein signaling 12 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23349096 731522 Rgs12 regulator of G-protein signaling 12 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23349096 731522 Rgs12 regulator of G-protein signaling 12 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:23349096 731522 Rgs12 regulator of G-protein signaling 12 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:23349096 731522 Rgs12 regulator of G-protein signaling 12 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23349096 731522 Rgs12 regulator of G-protein signaling 12 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:23349096 731522 Rgs12 regulator of G-protein signaling 12 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:23349096 731523 Pex11a peroxisomal biogenesis factor 11 alpha gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23169785 731523 Pex11a peroxisomal biogenesis factor 11 alpha gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23169785 731523 Pex11a peroxisomal biogenesis factor 11 alpha gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23169785 731523 Pex11a peroxisomal biogenesis factor 11 alpha gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:23169785 731523 Pex11a peroxisomal biogenesis factor 11 alpha gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23169785 731523 Pex11a peroxisomal biogenesis factor 11 alpha gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12417726 731523 Pex11a peroxisomal biogenesis factor 11 alpha gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12417726 731523 Pex11a peroxisomal biogenesis factor 11 alpha gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:12417726 731523 Pex11a peroxisomal biogenesis factor 11 alpha gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:23169785 731523 Pex11a peroxisomal biogenesis factor 11 alpha gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23169785 731523 Pex11a peroxisomal biogenesis factor 11 alpha gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23169785 731523 Pex11a peroxisomal biogenesis factor 11 alpha gene MP:0011969 abnormal circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23169785 731523 Pex11a peroxisomal biogenesis factor 11 alpha gene MP:0014010 abnormal peroxisome morphology IAGP N RGD:5509061 20230615 MGI PMID:12417726 731523 Pex11a peroxisomal biogenesis factor 11 alpha gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:12417726 731523 Pex11a peroxisomal biogenesis factor 11 alpha gene MP:0020847 abnormal peroxisome physiology IAGP N RGD:5509061 20230615 MGI PMID:12417726 731524 Pim3 proviral integration site 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15199164 731524 Pim3 proviral integration site 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15199164 731524 Pim3 proviral integration site 3 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:15199164 731524 Pim3 proviral integration site 3 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:15199164 731524 Pim3 proviral integration site 3 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 731524 Pim3 proviral integration site 3 gene MP:0003133 increased early pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 731524 Pim3 proviral integration site 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 731524 Pim3 proviral integration site 3 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15199164 731524 Pim3 proviral integration site 3 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15199164 731524 Pim3 proviral integration site 3 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 731524 Pim3 proviral integration site 3 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 731524 Pim3 proviral integration site 3 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15199164 731524 Pim3 proviral integration site 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15199164 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0001924 infertility IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0001925 male infertility IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0001926 female infertility IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20170525 MGI PMID:28031483 731526 Spdya speedy/RINGO cell cycle regulator family, member A gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20170525 MGI PMID:28031483 731527 Gdi2 GDP dissociation inhibitor 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 731527 Gdi2 GDP dissociation inhibitor 2 gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 731527 Gdi2 GDP dissociation inhibitor 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 731527 Gdi2 GDP dissociation inhibitor 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 731527 Gdi2 GDP dissociation inhibitor 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20240606 MGI PMID:35689892 731527 Gdi2 GDP dissociation inhibitor 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 731527 Gdi2 GDP dissociation inhibitor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20240606 MGI PMID:35689892 731527 Gdi2 GDP dissociation inhibitor 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731527 Gdi2 GDP dissociation inhibitor 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20240606 MGI PMID:35689892 731529 Slco1c1 solute carrier organic anion transporter family, member 1c1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22294745 731529 Slco1c1 solute carrier organic anion transporter family, member 1c1 gene MP:0005471 decreased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:22294745 731529 Slco1c1 solute carrier organic anion transporter family, member 1c1 gene MP:0005473 decreased triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:22294745 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:18845638 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18845638 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:18845638 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0002711 decreased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:18845638 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:18845638 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:18845638 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:18799753 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18063692 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18845638 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:18845638 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18845638 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19095739 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18845638 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18845638 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0006135 artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:18845638 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19095739 731530 Gper1 G protein-coupled estrogen receptor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19095739 731531 Nxph3 neurexophilin 3 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:16055736 731531 Nxph3 neurexophilin 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16055736 731531 Nxph3 neurexophilin 3 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16055736 731531 Nxph3 neurexophilin 3 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:16055736 731531 Nxph3 neurexophilin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16055736 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:18785974 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:18785974 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15263024 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10523604 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:18563383 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:21791433 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15263024 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9334367 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15024050 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:24021673 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17082625 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:12069389 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18563383 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16020505 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17082625 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:19084435 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20951970 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:18785974 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:18785974 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:15263024 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15263024 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:15263024 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002464 abnormal basophil physiology IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15263024 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:15263024 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:15263024 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0002879 increased cellular sensitivity to X-ray irradiation IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21262827 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18785974 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12069389 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0004503 decreased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19528538 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23109710 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24021673 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005046 absent spleen white pulp IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:18785974 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:20951970 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:21262803 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:21262827 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141211 MGI PMID:24633240 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20210506 MGI PMID:32381589 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0005673 decreased susceptibility to graft versus host disease IAGP N RGD:5509061 20141003 MGI PMID:24021673 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:23109710 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008041 absent NK T cells IAGP N RGD:5509061 20141003 MGI PMID:18785974 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:12586624 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19084435 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008046 absent NK cells IAGP N RGD:5509061 20141003 MGI PMID:12586624 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008046 absent NK cells IAGP N RGD:5509061 20141003 MGI PMID:17082625 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008046 absent NK cells IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008046 absent NK cells IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008046 absent NK cells IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008047 absent uterine NK cells IAGP N RGD:5509061 20141003 MGI PMID:12069389 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:12586624 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:17082625 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:12586624 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19528538 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23109710 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24021673 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24021673 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19528538 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23109710 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008122 decreased myeloid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:16020505 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008136 enlarged Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008348 absent gamma-delta T cells IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008348 absent gamma-delta T cells IAGP N RGD:5509061 20141003 MGI PMID:9334367 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008352 absent gamma-delta intraepithelial T cell IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008352 absent gamma-delta intraepithelial T cell IAGP N RGD:5509061 20141003 MGI PMID:9334367 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008356 abnormal gamma-delta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9334367 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008399 abnormal alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008464 absent peripheral lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:24021673 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:7831294 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20141003 MGI PMID:17082625 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:19084435 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16020505 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:8562967 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:12069389 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:12069389 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0009020 prolonged metestrus IAGP N RGD:5509061 20141003 MGI PMID:12069389 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:19528538 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20141003 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17082625 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0010250 absent thymus cortex IAGP N RGD:5509061 20160324 MGI PMID:18785974 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0010776 abnormal placenta metrial gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12069389 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0012529 abnormal decidua basalis morphology IAGP N RGD:5509061 20141003 MGI PMID:12069389 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0013587 absent thymus medulla IAGP N RGD:5509061 20160324 MGI PMID:18785974 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0013592 small thymus cortex IAGP N RGD:5509061 20150326 MGI PMID:7697543 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0014130 thymus cyst IAGP N RGD:5509061 20160324 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0014130 thymus cyst IAGP N RGD:5509061 20160324 MGI PMID:18785974 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:15879151 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:18785974 731534 Il2rg interleukin 2 receptor, gamma chain gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:24021673 731536 Hnrnph1 heterogeneous nuclear ribonucleoprotein H1 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20181227 MGI 731536 Hnrnph1 heterogeneous nuclear ribonucleoprotein H1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20181227 MGI 731536 Hnrnph1 heterogeneous nuclear ribonucleoprotein H1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20190502 MGI 731536 Hnrnph1 heterogeneous nuclear ribonucleoprotein H1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 731536 Hnrnph1 heterogeneous nuclear ribonucleoprotein H1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20181227 MGI 731536 Hnrnph1 heterogeneous nuclear ribonucleoprotein H1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731536 Hnrnph1 heterogeneous nuclear ribonucleoprotein H1 gene MP:0031304 impaired behavioral response to methamphetamine IAGP N RGD:5509061 20240328 MGI PMID:26658939 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11939592 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:14500732 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:11939592 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:14500732 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11939592 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14500732 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11939592 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:11939592 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:15769750 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:14500732 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20230601 MGI 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:14500732 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20230601 MGI 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14500732 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11939592 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0014010 abnormal peroxisome morphology IAGP N RGD:5509061 20200917 MGI PMID:14500732 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0020847 abnormal peroxisome physiology IAGP N RGD:5509061 20230615 MGI PMID:10336479 731537 Ehhadh enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:14500732 731539 Hoxa2 homeobox A2 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:10529419 731539 Hoxa2 homeobox A2 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15861402 731539 Hoxa2 homeobox A2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:15861402 731539 Hoxa2 homeobox A2 gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10529419 731539 Hoxa2 homeobox A2 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:11857791 731539 Hoxa2 homeobox A2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:11857792 731539 Hoxa2 homeobox A2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10529419 731539 Hoxa2 homeobox A2 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201231 MGI 731539 Hoxa2 homeobox A2 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:10529419 731539 Hoxa2 homeobox A2 gene MP:0000909 abnormal facial motor nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:23197710 731539 Hoxa2 homeobox A2 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:10230789 731539 Hoxa2 homeobox A2 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:12412013 731539 Hoxa2 homeobox A2 gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:23197710 731539 Hoxa2 homeobox A2 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:14960494 731539 Hoxa2 homeobox A2 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 731539 Hoxa2 homeobox A2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:10529419 731539 Hoxa2 homeobox A2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12412013 731539 Hoxa2 homeobox A2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10529419 731539 Hoxa2 homeobox A2 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11857791 731539 Hoxa2 homeobox A2 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11857792 731539 Hoxa2 homeobox A2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10529419 731539 Hoxa2 homeobox A2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11857791 731539 Hoxa2 homeobox A2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12412013 731539 Hoxa2 homeobox A2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0003110 absent malleus processus brevis IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0003168 abnormal scala vestibuli morphology IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:11857791 731539 Hoxa2 homeobox A2 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:11857792 731539 Hoxa2 homeobox A2 gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10529419 731539 Hoxa2 homeobox A2 gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:10529419 731539 Hoxa2 homeobox A2 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0004665 abnormal stapedial artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0004666 absent stapedial artery IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 731539 Hoxa2 homeobox A2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:11857791 731539 Hoxa2 homeobox A2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:11857792 731539 Hoxa2 homeobox A2 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10529419 731539 Hoxa2 homeobox A2 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:15861402 731539 Hoxa2 homeobox A2 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:12412013 731539 Hoxa2 homeobox A2 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 731539 Hoxa2 homeobox A2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11857791 731539 Hoxa2 homeobox A2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11857792 731539 Hoxa2 homeobox A2 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20211021 MGI 731539 Hoxa2 homeobox A2 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:10529419 731539 Hoxa2 homeobox A2 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0006018 abnormal tympanic membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0006033 abnormal external auditory canal morphology IAGP N RGD:5509061 20141003 MGI PMID:8565828 731539 Hoxa2 homeobox A2 gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20141003 MGI PMID:23408898 731539 Hoxa2 homeobox A2 gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:12412013 731539 Hoxa2 homeobox A2 gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0008378 small malleus processus brevis IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0008380 abnormal gonial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0008380 abnormal gonial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0008383 enlarged gonial bone IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0008386 absent styloid process IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0008386 absent styloid process IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 731539 Hoxa2 homeobox A2 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221208 MGI PMID:19653318 731539 Hoxa2 homeobox A2 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221208 MGI PMID:29218017 731539 Hoxa2 homeobox A2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221208 MGI PMID:19653318 731539 Hoxa2 homeobox A2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221208 MGI PMID:29218017 731539 Hoxa2 homeobox A2 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20221208 MGI PMID:19653318 731539 Hoxa2 homeobox A2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221208 MGI PMID:19653318 731539 Hoxa2 homeobox A2 gene MP:0009889 persistence of medial edge epithelium during palatal shelf fusion IAGP N RGD:5509061 20221208 MGI PMID:29218017 731539 Hoxa2 homeobox A2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:10529419 731539 Hoxa2 homeobox A2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0009909 bifid tongue IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0009909 bifid tongue IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20141003 MGI PMID:12412013 731539 Hoxa2 homeobox A2 gene MP:0009915 absent hyoid bone lesser horns IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0009915 absent hyoid bone lesser horns IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:10230789 731539 Hoxa2 homeobox A2 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20210128 MGI 731539 Hoxa2 homeobox A2 gene MP:0010892 increased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:23197710 731539 Hoxa2 homeobox A2 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12412013 731539 Hoxa2 homeobox A2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10230789 731539 Hoxa2 homeobox A2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10529419 731539 Hoxa2 homeobox A2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11857791 731539 Hoxa2 homeobox A2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11857792 731539 Hoxa2 homeobox A2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731539 Hoxa2 homeobox A2 gene MP:0012490 abnormal cochlear VIII nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:23408898 731539 Hoxa2 homeobox A2 gene MP:0012786 increased rhombomere 1 size IAGP N RGD:5509061 20141003 MGI PMID:10230789 731539 Hoxa2 homeobox A2 gene MP:0012788 abnormal rhombomere 2 morphology IAGP N RGD:5509061 20141003 MGI PMID:10230789 731539 Hoxa2 homeobox A2 gene MP:0012788 abnormal rhombomere 2 morphology IAGP N RGD:5509061 20141003 MGI PMID:12412013 731539 Hoxa2 homeobox A2 gene MP:0012792 abnormal rhombomere 3 morphology IAGP N RGD:5509061 20141003 MGI PMID:10230789 731539 Hoxa2 homeobox A2 gene MP:0012792 abnormal rhombomere 3 morphology IAGP N RGD:5509061 20141003 MGI PMID:12412013 731539 Hoxa2 homeobox A2 gene MP:0012793 decreased rhombomere 3 size IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0012816 abnormal rhombomere boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0014563 duplicated tympanic ring IAGP N RGD:5509061 20241031 MGI PMID:16221728 731539 Hoxa2 homeobox A2 gene MP:0014563 duplicated tympanic ring IAGP N RGD:5509061 20241031 MGI PMID:8565828 731539 Hoxa2 homeobox A2 gene MP:0030108 abnormal incudostapedial joint morphology IAGP N RGD:5509061 20170928 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0030119 abnormal retrotympanic process morphology IAGP N RGD:5509061 20171005 MGI PMID:11578867 731539 Hoxa2 homeobox A2 gene MP:0030119 abnormal retrotympanic process morphology IAGP N RGD:5509061 20171005 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0030123 small middle ear ossicles IAGP N RGD:5509061 20171005 MGI PMID:10529419 731539 Hoxa2 homeobox A2 gene MP:0030150 absent stylohyoid muscle IAGP N RGD:5509061 20171005 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0030154 abnormal tympanic cavity morphology IAGP N RGD:5509061 20171005 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0030158 absent stapedius muscle IAGP N RGD:5509061 20171005 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0030159 abnormal tensor tympani muscle morphology IAGP N RGD:5509061 20171005 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0030211 abnormal styloglossus muscle morphology IAGP N RGD:5509061 20171019 MGI PMID:10529419 731539 Hoxa2 homeobox A2 gene MP:0030227 abnormal tubotympanic recess morphology IAGP N RGD:5509061 20171019 MGI PMID:7903600 731539 Hoxa2 homeobox A2 gene MP:0030320 abnormal temporal bone tympanic part morphology IAGP N RGD:5509061 20171109 MGI PMID:7903601 731539 Hoxa2 homeobox A2 gene MP:0030465 absent oval window IAGP N RGD:5509061 20221208 MGI PMID:11578867 731541 Kif3c kinesin family member 3C gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 731541 Kif3c kinesin family member 3C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11463814 731541 Kif3c kinesin family member 3C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16337628 731541 Kif3c kinesin family member 3C gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 731541 Kif3c kinesin family member 3C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731541 Kif3c kinesin family member 3C gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20211021 MGI 731543 Nox4 NADPH oxidase 4 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 731543 Nox4 NADPH oxidase 4 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:21391892 731543 Nox4 NADPH oxidase 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20921387 731543 Nox4 NADPH oxidase 4 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:20921387 731543 Nox4 NADPH oxidase 4 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 731543 Nox4 NADPH oxidase 4 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20713697 731543 Nox4 NADPH oxidase 4 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20151126 MGI PMID:23749776 731543 Nox4 NADPH oxidase 4 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20877715 731543 Nox4 NADPH oxidase 4 gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20713697 731543 Nox4 NADPH oxidase 4 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20210121 MGI PMID:33086058 731543 Nox4 NADPH oxidase 4 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:20713697 731543 Nox4 NADPH oxidase 4 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:20877715 731543 Nox4 NADPH oxidase 4 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:21391892 731543 Nox4 NADPH oxidase 4 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:20921387 731543 Nox4 NADPH oxidase 4 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:20713697 731543 Nox4 NADPH oxidase 4 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:20921387 731543 Nox4 NADPH oxidase 4 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 731543 Nox4 NADPH oxidase 4 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20713697 731543 Nox4 NADPH oxidase 4 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20713697 731543 Nox4 NADPH oxidase 4 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20921387 731543 Nox4 NADPH oxidase 4 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:20713697 731543 Nox4 NADPH oxidase 4 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21391892 731543 Nox4 NADPH oxidase 4 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:20877715 731543 Nox4 NADPH oxidase 4 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:20877715 731543 Nox4 NADPH oxidase 4 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20210121 MGI PMID:33086058 731543 Nox4 NADPH oxidase 4 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20210121 MGI PMID:33086058 731543 Nox4 NADPH oxidase 4 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20210121 MGI PMID:33086058 731543 Nox4 NADPH oxidase 4 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21391892 731543 Nox4 NADPH oxidase 4 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20713697 731543 Nox4 NADPH oxidase 4 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210121 MGI PMID:33086058 731543 Nox4 NADPH oxidase 4 gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:21391892 731543 Nox4 NADPH oxidase 4 gene MP:0011371 decreased kidney apoptosis IAGP N RGD:5509061 20210121 MGI PMID:33086058 731543 Nox4 NADPH oxidase 4 gene MP:0011372 decreased renal tubule apoptosis IAGP N RGD:5509061 20210121 MGI PMID:33086058 731543 Nox4 NADPH oxidase 4 gene MP:0031385 enhanced blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:20877715 731543 Nox4 NADPH oxidase 4 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:20713697 731549 Rasd1 RAS, dexamethasone-induced 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20160811 MGI 731549 Rasd1 RAS, dexamethasone-induced 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20160811 MGI 731549 Rasd1 RAS, dexamethasone-induced 1 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23426685 731549 Rasd1 RAS, dexamethasone-induced 1 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:23426685 731549 Rasd1 RAS, dexamethasone-induced 1 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:15339652 731549 Rasd1 RAS, dexamethasone-induced 1 gene MP:0020474 advanced circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:15339652 731549 Rasd1 RAS, dexamethasone-induced 1 gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:15339652 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:20826436 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0000921 demyelination IAGP N RGD:5509061 20200528 MGI PMID:30624206 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0001393 ataxia IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20826436 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0001405 impaired coordination IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200528 MGI PMID:30624206 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0002083 premature death IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20826436 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20160331 MGI PMID:23056417 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0002183 gliosis IAGP N RGD:5509061 20200528 MGI PMID:30624206 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20141003 MGI 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0002763 ectopic Bergmann glia cells IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0002834 decreased heart weight IEA N RGD:5509061 20160804 MGI 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20200528 MGI PMID:30624206 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20160331 MGI PMID:23056417 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:20826436 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:20826436 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160804 MGI 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20141003 MGI 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:20826436 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:20826436 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20200528 MGI PMID:30624206 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0008569 lethality at weaning IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20826436 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20160331 MGI PMID:23056417 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0009978 abnormal cerebellum white matter morphology IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200528 MGI PMID:30624206 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:20826436 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0010892 increased oligodendrocyte progenitor number IAGP N RGD:5509061 20180628 MGI PMID:26974157 731554 Eif2b5 eukaryotic translation initiation factor 2B, subunit 5 epsilon gene MP:0014429 increased hyaluronic acid level IAGP N RGD:5509061 20240425 MGI PMID:26974157 731555 Gck glucokinase gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7553875 731555 Gck glucokinase gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:17353190 731555 Gck glucokinase gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20210429 MGI PMID:33558985 731555 Gck glucokinase gene MP:0001260 increased body weight IEA N RGD:5509061 20141003 MGI 731555 Gck glucokinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15102714 731555 Gck glucokinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19952346 731555 Gck glucokinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22698525 731555 Gck glucokinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9062343 731555 Gck glucokinase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:7553875 731555 Gck glucokinase gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:9867845 731555 Gck glucokinase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12420138 731555 Gck glucokinase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15102714 731555 Gck glucokinase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15161764 731555 Gck glucokinase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:17353190 731555 Gck glucokinase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:18056790 731555 Gck glucokinase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19952346 731555 Gck glucokinase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21921030 731555 Gck glucokinase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:22698525 731555 Gck glucokinase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:7553875 731555 Gck glucokinase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:7665557 731555 Gck glucokinase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:8530440 731555 Gck glucokinase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:9867845 731555 Gck glucokinase gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141106 MGI PMID:24838824 731555 Gck glucokinase gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17353190 731555 Gck glucokinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19952346 731555 Gck glucokinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8530440 731555 Gck glucokinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9062343 731555 Gck glucokinase gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:15102714 731555 Gck glucokinase gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:19952346 731555 Gck glucokinase gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:8530440 731555 Gck glucokinase gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17353190 731555 Gck glucokinase gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7665557 731555 Gck glucokinase gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9867845 731555 Gck glucokinase gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19952346 731555 Gck glucokinase gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9062343 731555 Gck glucokinase gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9867845 731555 Gck glucokinase gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20210429 MGI PMID:33558985 731555 Gck glucokinase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15102714 731555 Gck glucokinase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19952346 731555 Gck glucokinase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15102714 731555 Gck glucokinase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:8530440 731555 Gck glucokinase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:9867845 731555 Gck glucokinase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15102714 731555 Gck glucokinase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21921030 731555 Gck glucokinase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22698525 731555 Gck glucokinase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:8530440 731555 Gck glucokinase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9867845 731555 Gck glucokinase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 731555 Gck glucokinase gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20210429 MGI PMID:33558985 731555 Gck glucokinase gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19952346 731555 Gck glucokinase gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:22698525 731555 Gck glucokinase gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:8530440 731555 Gck glucokinase gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:9867845 731555 Gck glucokinase gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20190530 MGI PMID:24447392 731555 Gck glucokinase gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8530440 731555 Gck glucokinase gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20190530 MGI PMID:24447392 731555 Gck glucokinase gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20210429 MGI PMID:33558985 731555 Gck glucokinase gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17353190 731555 Gck glucokinase gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20190530 MGI PMID:24447392 731555 Gck glucokinase gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:22698525 731555 Gck glucokinase gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22698525 731555 Gck glucokinase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15102714 731555 Gck glucokinase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15161764 731555 Gck glucokinase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15569412 731555 Gck glucokinase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17353190 731555 Gck glucokinase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19952346 731555 Gck glucokinase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22698525 731555 Gck glucokinase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:7553875 731555 Gck glucokinase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:7665557 731555 Gck glucokinase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:8530440 731555 Gck glucokinase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:9062343 731555 Gck glucokinase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:9867845 731555 Gck glucokinase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141106 MGI PMID:24838824 731555 Gck glucokinase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20190530 MGI PMID:24447392 731555 Gck glucokinase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210429 MGI PMID:33558985 731555 Gck glucokinase gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:19952346 731555 Gck glucokinase gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:9062343 731555 Gck glucokinase gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:9867845 731555 Gck glucokinase gene MP:0005331 insulin resistance IAGP N RGD:5509061 20190530 MGI PMID:24447392 731555 Gck glucokinase gene MP:0005439 decreased glycogen level IAGP N RGD:5509061 20141003 MGI PMID:9867845 731555 Gck glucokinase gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9062343 731555 Gck glucokinase gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15569412 731555 Gck glucokinase gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22698525 731555 Gck glucokinase gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:9867845 731555 Gck glucokinase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17353190 731555 Gck glucokinase gene MP:0006353 increased glycosylated hemoglobin level IAGP N RGD:5509061 20141003 MGI PMID:15102714 731555 Gck glucokinase gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:9062343 731555 Gck glucokinase gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20210429 MGI PMID:33558985 731555 Gck glucokinase gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:19952346 731555 Gck glucokinase gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:22698525 731555 Gck glucokinase gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20210429 MGI PMID:33558985 731555 Gck glucokinase gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19952346 731555 Gck glucokinase gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:22698525 731555 Gck glucokinase gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20181227 MGI 731555 Gck glucokinase gene MP:0010147 abnormal endocrine pancreas physiology IAGP N RGD:5509061 20210429 MGI PMID:33558985 731555 Gck glucokinase gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20190530 MGI PMID:24447392 731555 Gck glucokinase gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:15102714 731555 Gck glucokinase gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:7553875 731555 Gck glucokinase gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:9867845 731555 Gck glucokinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17353190 731555 Gck glucokinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7553875 731555 Gck glucokinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8530440 731555 Gck glucokinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9867845 731555 Gck glucokinase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9867845 731555 Gck glucokinase gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7665557 731555 Gck glucokinase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 731555 Gck glucokinase gene MP:0011606 decreased glucokinase activity IAGP N RGD:5509061 20141003 MGI PMID:17353190 731555 Gck glucokinase gene MP:0011606 decreased glucokinase activity IAGP N RGD:5509061 20141003 MGI PMID:22698525 731555 Gck glucokinase gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20190530 MGI PMID:24447392 731555 Gck glucokinase gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20190530 MGI PMID:24447392 731555 Gck glucokinase gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20210429 MGI PMID:33558985 731555 Gck glucokinase gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20190530 MGI PMID:24447392 731555 Gck glucokinase gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20210429 MGI PMID:33558985 731555 Gck glucokinase gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20190530 MGI PMID:24447392 731555 Gck glucokinase gene MP:0030970 ketosis IAGP N RGD:5509061 20190815 MGI PMID:8530440 731555 Gck glucokinase gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:7553875 731557 Psmc4 proteasome (prosome, macropain) 26S subunit, ATPase, 4 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:23095749 731557 Psmc4 proteasome (prosome, macropain) 26S subunit, ATPase, 4 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23095749 731557 Psmc4 proteasome (prosome, macropain) 26S subunit, ATPase, 4 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23095749 731557 Psmc4 proteasome (prosome, macropain) 26S subunit, ATPase, 4 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:23095749 731557 Psmc4 proteasome (prosome, macropain) 26S subunit, ATPase, 4 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:23095749 731557 Psmc4 proteasome (prosome, macropain) 26S subunit, ATPase, 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23095749 731557 Psmc4 proteasome (prosome, macropain) 26S subunit, ATPase, 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23095749 731557 Psmc4 proteasome (prosome, macropain) 26S subunit, ATPase, 4 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:23095749 731557 Psmc4 proteasome (prosome, macropain) 26S subunit, ATPase, 4 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:10945464 731557 Psmc4 proteasome (prosome, macropain) 26S subunit, ATPase, 4 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10945464 731557 Psmc4 proteasome (prosome, macropain) 26S subunit, ATPase, 4 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23095749 731557 Psmc4 proteasome (prosome, macropain) 26S subunit, ATPase, 4 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23095749 731557 Psmc4 proteasome (prosome, macropain) 26S subunit, ATPase, 4 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23095749 731557 Psmc4 proteasome (prosome, macropain) 26S subunit, ATPase, 4 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10945464 731560 Asl argininosuccinate lyase gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0000380 small hair follicles IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0001221 epidermal atrophy IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:12559843 731560 Asl argininosuccinate lyase gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:12559843 731560 Asl argininosuccinate lyase gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:12559843 731560 Asl argininosuccinate lyase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:12559843 731560 Asl argininosuccinate lyase gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:12559843 731560 Asl argininosuccinate lyase gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0010177 acanthocytosis IAGP N RGD:5509061 20141003 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12559843 731560 Asl argininosuccinate lyase gene MP:0020836 increased circulating citrulline level IAGP N RGD:5509061 20180712 MGI PMID:12559843 731560 Asl argininosuccinate lyase gene MP:0020836 increased circulating citrulline level IAGP N RGD:5509061 20180712 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0030662 decreased circulating arginine level IAGP N RGD:5509061 20180920 MGI PMID:12559843 731560 Asl argininosuccinate lyase gene MP:0030662 decreased circulating arginine level IAGP N RGD:5509061 20180920 MGI PMID:22081021 731560 Asl argininosuccinate lyase gene MP:0030709 increased circulating glutamine level IAGP N RGD:5509061 20180920 MGI PMID:12559843 731563 Msx1 msh homeobox 1 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:12701100 731563 Msx1 msh homeobox 1 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10742104 731563 Msx1 msh homeobox 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0000082 overlapping parietal bones IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0000084 abnormal fontanelle morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0000094 absent alveolar process IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0000094 absent alveolar process IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0000094 absent alveolar process IAGP N RGD:5509061 20141003 MGI PMID:9256350 731563 Msx1 msh homeobox 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10512191 731563 Msx1 msh homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17654563 731563 Msx1 msh homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:18442049 731563 Msx1 msh homeobox 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0000114 cleft chin IAGP N RGD:5509061 20141003 MGI PMID:9256350 731563 Msx1 msh homeobox 1 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:10742104 731563 Msx1 msh homeobox 1 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:22084104 731563 Msx1 msh homeobox 1 gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:9256350 731563 Msx1 msh homeobox 1 gene MP:0000128 growth retardation of molars IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0000128 growth retardation of molars IAGP N RGD:5509061 20141003 MGI PMID:9256350 731563 Msx1 msh homeobox 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20150903 MGI PMID:18667074 731563 Msx1 msh homeobox 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20150903 MGI PMID:18667074 731563 Msx1 msh homeobox 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:10742104 731563 Msx1 msh homeobox 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:18442049 731563 Msx1 msh homeobox 1 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:9256350 731563 Msx1 msh homeobox 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9256350 731563 Msx1 msh homeobox 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:18442049 731563 Msx1 msh homeobox 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:9256350 731563 Msx1 msh homeobox 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:15930102 731563 Msx1 msh homeobox 1 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15930102 731563 Msx1 msh homeobox 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:15930102 731563 Msx1 msh homeobox 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:15930102 731563 Msx1 msh homeobox 1 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:15930102 731563 Msx1 msh homeobox 1 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:23090744 731563 Msx1 msh homeobox 1 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:10742104 731563 Msx1 msh homeobox 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:12874124 731563 Msx1 msh homeobox 1 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:12874124 731563 Msx1 msh homeobox 1 gene MP:0000829 dilated fourth ventricle IAGP N RGD:5509061 20141003 MGI PMID:12874124 731563 Msx1 msh homeobox 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:12874124 731563 Msx1 msh homeobox 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12874124 731563 Msx1 msh homeobox 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18442049 731563 Msx1 msh homeobox 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:23090744 731563 Msx1 msh homeobox 1 gene MP:0000923 abnormal roof plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12874124 731563 Msx1 msh homeobox 1 gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20150205 MGI PMID:24715462 731563 Msx1 msh homeobox 1 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20211021 MGI 731563 Msx1 msh homeobox 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9256350 731563 Msx1 msh homeobox 1 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:15930102 731563 Msx1 msh homeobox 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12874124 731563 Msx1 msh homeobox 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20150205 MGI PMID:24715462 731563 Msx1 msh homeobox 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:12874124 731563 Msx1 msh homeobox 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21693521 731563 Msx1 msh homeobox 1 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9256350 731563 Msx1 msh homeobox 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23090744 731563 Msx1 msh homeobox 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18442049 731563 Msx1 msh homeobox 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:23090744 731563 Msx1 msh homeobox 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:23090744 731563 Msx1 msh homeobox 1 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20150205 MGI PMID:24715462 731563 Msx1 msh homeobox 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12874124 731563 Msx1 msh homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:24715462 731563 Msx1 msh homeobox 1 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21693521 731563 Msx1 msh homeobox 1 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:12874124 731563 Msx1 msh homeobox 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 731563 Msx1 msh homeobox 1 gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:12874124 731563 Msx1 msh homeobox 1 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0003110 absent malleus processus brevis IAGP N RGD:5509061 20141003 MGI PMID:10512191 731563 Msx1 msh homeobox 1 gene MP:0003110 absent malleus processus brevis IAGP N RGD:5509061 20141003 MGI PMID:12701100 731563 Msx1 msh homeobox 1 gene MP:0003110 absent malleus processus brevis IAGP N RGD:5509061 20141003 MGI PMID:23090744 731563 Msx1 msh homeobox 1 gene MP:0003110 absent malleus processus brevis IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0003110 absent malleus processus brevis IAGP N RGD:5509061 20141003 MGI PMID:9256350 731563 Msx1 msh homeobox 1 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:12701100 731563 Msx1 msh homeobox 1 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:23090744 731563 Msx1 msh homeobox 1 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:9256350 731563 Msx1 msh homeobox 1 gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21693521 731563 Msx1 msh homeobox 1 gene MP:0003842 abnormal metopic suture morphology IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0003931 absent molars IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:18442049 731563 Msx1 msh homeobox 1 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0004181 abnormal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21693521 731563 Msx1 msh homeobox 1 gene MP:0004343 small scapula IAGP N RGD:5509061 20141003 MGI PMID:15930102 731563 Msx1 msh homeobox 1 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15930102 731563 Msx1 msh homeobox 1 gene MP:0004575 small limb buds IAGP N RGD:5509061 20141003 MGI PMID:15930102 731563 Msx1 msh homeobox 1 gene MP:0004691 absent pubis IAGP N RGD:5509061 20141003 MGI PMID:15930102 731563 Msx1 msh homeobox 1 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0004790 absent upper incisors IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0004791 absent lower incisors IAGP N RGD:5509061 20170928 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15930102 731563 Msx1 msh homeobox 1 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12701100 731563 Msx1 msh homeobox 1 gene MP:0005382 craniofacial phenotype IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:10512191 731563 Msx1 msh homeobox 1 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12701100 731563 Msx1 msh homeobox 1 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:10512191 731563 Msx1 msh homeobox 1 gene MP:0006033 abnormal external auditory canal morphology IAGP N RGD:5509061 20141003 MGI PMID:12701100 731563 Msx1 msh homeobox 1 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:18442049 731563 Msx1 msh homeobox 1 gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0008372 small malleus IAGP N RGD:5509061 20141003 MGI PMID:12701100 731563 Msx1 msh homeobox 1 gene MP:0008373 short malleus IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0008377 absent malleus manubrium IAGP N RGD:5509061 20141003 MGI PMID:12701100 731563 Msx1 msh homeobox 1 gene MP:0008379 absent malleus head IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20150903 MGI PMID:18667074 731563 Msx1 msh homeobox 1 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:15743757 731563 Msx1 msh homeobox 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:23090744 731563 Msx1 msh homeobox 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0009707 absent external auditory canal IAGP N RGD:5509061 20141003 MGI PMID:10512191 731563 Msx1 msh homeobox 1 gene MP:0009716 abnormal subcommissural organ morphology IAGP N RGD:5509061 20141003 MGI PMID:12874124 731563 Msx1 msh homeobox 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0009843 decreased neural crest cell number IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:23090744 731563 Msx1 msh homeobox 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:9256350 731563 Msx1 msh homeobox 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0009913 abnormal hyoid bone greater horn morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0010355 abnormal first pharyngeal arch artery morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0010356 abnormal second pharyngeal arch artery morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20150903 MGI PMID:18667074 731563 Msx1 msh homeobox 1 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0010478 intracranial aneurysm IAGP N RGD:5509061 20141003 MGI PMID:21693521 731563 Msx1 msh homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16330189 731563 Msx1 msh homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7914451 731563 Msx1 msh homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9256350 731563 Msx1 msh homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15930102 731563 Msx1 msh homeobox 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18442049 731563 Msx1 msh homeobox 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731563 Msx1 msh homeobox 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12874124 731563 Msx1 msh homeobox 1 gene MP:0011513 abnormal vertebral artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21693521 731563 Msx1 msh homeobox 1 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 731563 Msx1 msh homeobox 1 gene MP:0030154 abnormal tympanic cavity morphology IAGP N RGD:5509061 20171005 MGI PMID:10512191 731563 Msx1 msh homeobox 1 gene MP:0030187 abnormal epitympanic recess morphology IAGP N RGD:5509061 20171012 MGI PMID:10512191 731563 Msx1 msh homeobox 1 gene MP:0030336 third pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0030341 fourth pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0030579 thoracoabdominoschisis IAGP N RGD:5509061 20180607 MGI PMID:18442049 731563 Msx1 msh homeobox 1 gene MP:0030579 thoracoabdominoschisis IAGP N RGD:5509061 20180607 MGI PMID:23090744 731563 Msx1 msh homeobox 1 gene MP:0030608 decreased tooth number IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:23090744 731563 Msx1 msh homeobox 1 gene MP:0030870 abnormal superior horn of thyroid cartilage morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0030871 abnormal inferior horn of thyroid cartilage morphology IAGP N RGD:5509061 20220714 MGI PMID:34615475 731563 Msx1 msh homeobox 1 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20191128 MGI PMID:18667074 731565 Xylt2 xylosyltransferase II gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:17517600 731565 Xylt2 xylosyltransferase II gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:17517600 731565 Xylt2 xylosyltransferase II gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:17517600 731565 Xylt2 xylosyltransferase II gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17517600 731565 Xylt2 xylosyltransferase II gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:17517600 731565 Xylt2 xylosyltransferase II gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17517600 731565 Xylt2 xylosyltransferase II gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17517600 731565 Xylt2 xylosyltransferase II gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:17517600 731565 Xylt2 xylosyltransferase II gene MP:0005083 abnormal biliary tract morphology IAGP N RGD:5509061 20141003 MGI PMID:17517600 731565 Xylt2 xylosyltransferase II gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17517600 731565 Xylt2 xylosyltransferase II gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17517600 731566 Cttn cortactin gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20004659 731566 Cttn cortactin gene MP:0000745 tremors IEA N RGD:5509061 20201022 MGI 731566 Cttn cortactin gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21788407 731566 Cttn cortactin gene MP:0002210 abnormal sex determination IAGP N RGD:5509061 20141003 MGI PMID:21788407 731566 Cttn cortactin gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:21788407 731566 Cttn cortactin gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:21788407 731566 Cttn cortactin gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:21788407 731566 Cttn cortactin gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:20004659 731566 Cttn cortactin gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:21788407 731566 Cttn cortactin gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21788407 731566 Cttn cortactin gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:20004659 731566 Cttn cortactin gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:20004659 731566 Cttn cortactin gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:21788407 731566 Cttn cortactin gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20004659 731566 Cttn cortactin gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21788407 731566 Cttn cortactin gene MP:0011131 abnormal lung endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21788407 731566 Cttn cortactin gene MP:0012738 abnormal secondary polar body morphology IAGP N RGD:5509061 20141003 MGI PMID:20004659 731566 Cttn cortactin gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 731568 Timeless timeless circadian clock 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10903565 731568 Timeless timeless circadian clock 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10359811 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11455125 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9647244 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:9736029 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20160804 MGI 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12163535 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9688988 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:7990930 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9551933 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15289505 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12370348 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:9647244 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9551933 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:14661063 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16988041 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11292619 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180906 MGI PMID:29618659 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002329 abnormal blood gas level IAGP N RGD:5509061 20141003 MGI PMID:17435079 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002333 abnormal lung compliance IAGP N RGD:5509061 20141003 MGI PMID:17435079 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002343 abnormal lymph node cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9647244 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002345 abnormal lymph node primary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9647244 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002346 abnormal lymph node secondary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9647244 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9820556 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10595943 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:7990930 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10359811 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17435079 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:19285115 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002933 joint inflammation IAGP N RGD:5509061 20180906 MGI PMID:29618659 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20180906 MGI PMID:29618659 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20141003 MGI PMID:11455125 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:10779546 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20180906 MGI PMID:29618659 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11292619 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:10204494 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:12133972 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20141003 MGI PMID:10204494 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20180906 MGI PMID:29618659 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:12205053 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12205053 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:10064079 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:10064079 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10946317 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10946317 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:8673925 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0004822 decreased susceptibility to experimental autoimmune uveoretinitis IAGP N RGD:5509061 20141003 MGI PMID:10509653 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:10595943 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9647244 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9647244 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0005018 decreased T cell number IEA N RGD:5509061 20160804 MGI 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20180906 MGI PMID:29618659 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:10329607 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:14617760 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11739497 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0005190 osteomyelitis IAGP N RGD:5509061 20141003 MGI PMID:10595943 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:10359811 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:9647244 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20141003 MGI 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10946317 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0005580 periinsulitis IAGP N RGD:5509061 20141003 MGI PMID:10946317 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20180906 MGI PMID:29618659 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9846974 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:8673925 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20141003 MGI PMID:9736029 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20180906 MGI PMID:29618659 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:9647244 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:8673925 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:9647244 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:10064079 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0008523 absent lymph node germinal center IAGP N RGD:5509061 20141003 MGI PMID:9647244 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:9551933 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20180906 MGI PMID:29618659 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20180906 MGI PMID:29618659 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11739497 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:11739497 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:9551933 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9846974 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0008918 microgliosis IAGP N RGD:5509061 20161201 MGI PMID:16988041 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9688988 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0010053 decreased grip strength IEA N RGD:5509061 20141003 MGI 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16282134 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0010205 abnormal oligodendrocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9736029 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12771125 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:12205053 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:9688988 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:16079187 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0013251 dental pulp necrosis IAGP N RGD:5509061 20141003 MGI PMID:10595943 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20180906 MGI PMID:29618659 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0020449 decreased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:8673925 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200625 MGI PMID:27663205 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0030012 impaired central nervous system regeneration IAGP N RGD:5509061 20170713 MGI PMID:11517251 731571 Tnfrsf1b tumor necrosis factor receptor superfamily, member 1b gene MP:0031124 aortic valve inflammation IAGP N RGD:5509061 20200917 MGI PMID:29618659 731573 Ppm1a protein phosphatase 1A, magnesium dependent, alpha isoform gene MP:0001513 limb grasping IEA N RGD:5509061 20160421 MGI 731573 Ppm1a protein phosphatase 1A, magnesium dependent, alpha isoform gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20150305 MGI PMID:25196308 731573 Ppm1a protein phosphatase 1A, magnesium dependent, alpha isoform gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:21990361 731573 Ppm1a protein phosphatase 1A, magnesium dependent, alpha isoform gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 731573 Ppm1a protein phosphatase 1A, magnesium dependent, alpha isoform gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:21990361 731573 Ppm1a protein phosphatase 1A, magnesium dependent, alpha isoform gene MP:0003711 pathological neovascularization IAGP N RGD:5509061 20150305 MGI PMID:25196308 731573 Ppm1a protein phosphatase 1A, magnesium dependent, alpha isoform gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20190502 MGI 731573 Ppm1a protein phosphatase 1A, magnesium dependent, alpha isoform gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:21990361 731573 Ppm1a protein phosphatase 1A, magnesium dependent, alpha isoform gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20150305 MGI PMID:25196308 731573 Ppm1a protein phosphatase 1A, magnesium dependent, alpha isoform gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20150305 MGI PMID:25196308 731573 Ppm1a protein phosphatase 1A, magnesium dependent, alpha isoform gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 731573 Ppm1a protein phosphatase 1A, magnesium dependent, alpha isoform gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 731573 Ppm1a protein phosphatase 1A, magnesium dependent, alpha isoform gene MP:0012193 increased keratinocyte migration IAGP N RGD:5509061 20141204 MGI PMID:21990361 731573 Ppm1a protein phosphatase 1A, magnesium dependent, alpha isoform gene MP:0012194 decreased keratinocyte migration IAGP N RGD:5509061 20141204 MGI PMID:21990361 731573 Ppm1a protein phosphatase 1A, magnesium dependent, alpha isoform gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 731574 Pag1 phosphoprotein associated with glycosphingolipid microdomains 1 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16166631 731574 Pag1 phosphoprotein associated with glycosphingolipid microdomains 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21915273 731576 Ackr2 atypical chemokine receptor 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:15750596 731576 Ackr2 atypical chemokine receptor 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15789340 731578 Fbn1 fibrillin 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22374917 731578 Fbn1 fibrillin 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22374917 731578 Fbn1 fibrillin 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:15254584 731578 Fbn1 fibrillin 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:15254584 731578 Fbn1 fibrillin 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:21152435 731578 Fbn1 fibrillin 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230601 MGI 731578 Fbn1 fibrillin 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:7721853 731578 Fbn1 fibrillin 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:8221765 731578 Fbn1 fibrillin 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:9326947 731578 Fbn1 fibrillin 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:8070538 731578 Fbn1 fibrillin 1 gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:4048170 731578 Fbn1 fibrillin 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:7704626 731578 Fbn1 fibrillin 1 gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:1433576 731578 Fbn1 fibrillin 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:21152435 731578 Fbn1 fibrillin 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:6971670 731578 Fbn1 fibrillin 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:12598898 731578 Fbn1 fibrillin 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:1587342 731578 Fbn1 fibrillin 1 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9326947 731578 Fbn1 fibrillin 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:11168809 731578 Fbn1 fibrillin 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:12598898 731578 Fbn1 fibrillin 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:15254584 731578 Fbn1 fibrillin 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:18339630 731578 Fbn1 fibrillin 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:6562869 731578 Fbn1 fibrillin 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:6971670 731578 Fbn1 fibrillin 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:7704626 731578 Fbn1 fibrillin 1 gene MP:0001191 abnormal skin condition IEA N RGD:5509061 20111116 MGI 731578 Fbn1 fibrillin 1 gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:7704626 731578 Fbn1 fibrillin 1 gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:8723723 731578 Fbn1 fibrillin 1 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:11168809 731578 Fbn1 fibrillin 1 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:22242013 731578 Fbn1 fibrillin 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10931876 731578 Fbn1 fibrillin 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22242013 731578 Fbn1 fibrillin 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7359004 731578 Fbn1 fibrillin 1 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:22242013 731578 Fbn1 fibrillin 1 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:7359004 731578 Fbn1 fibrillin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200402 MGI PMID:29106398 731578 Fbn1 fibrillin 1 gene MP:0001267 enlarged chest IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7704626 731578 Fbn1 fibrillin 1 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:12485443 731578 Fbn1 fibrillin 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15254584 731578 Fbn1 fibrillin 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:8723723 731578 Fbn1 fibrillin 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:1433576 731578 Fbn1 fibrillin 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12598898 731578 Fbn1 fibrillin 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:21152435 731578 Fbn1 fibrillin 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:6971670 731578 Fbn1 fibrillin 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:7271067 731578 Fbn1 fibrillin 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:10486156 731578 Fbn1 fibrillin 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:12598898 731578 Fbn1 fibrillin 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:1587342 731578 Fbn1 fibrillin 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:21152435 731578 Fbn1 fibrillin 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:6562869 731578 Fbn1 fibrillin 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:7271067 731578 Fbn1 fibrillin 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:9326947 731578 Fbn1 fibrillin 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:22242013 731578 Fbn1 fibrillin 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:6847727 731578 Fbn1 fibrillin 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:7359004 731578 Fbn1 fibrillin 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11168809 731578 Fbn1 fibrillin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12598898 731578 Fbn1 fibrillin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21152435 731578 Fbn1 fibrillin 1 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20200402 MGI PMID:29106398 731578 Fbn1 fibrillin 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:22374917 731578 Fbn1 fibrillin 1 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:6971670 731578 Fbn1 fibrillin 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:1576433 731578 Fbn1 fibrillin 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:1587342 731578 Fbn1 fibrillin 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:6562869 731578 Fbn1 fibrillin 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:6971670 731578 Fbn1 fibrillin 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:7271067 731578 Fbn1 fibrillin 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:9326947 731578 Fbn1 fibrillin 1 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22374917 731578 Fbn1 fibrillin 1 gene MP:0002433 abnormal T-helper 1 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:22242013 731578 Fbn1 fibrillin 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230119 MGI 731578 Fbn1 fibrillin 1 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:22242013 731578 Fbn1 fibrillin 1 gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:7704626 731578 Fbn1 fibrillin 1 gene MP:0002964 aortic elastic tissue lesions IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:20729550 731578 Fbn1 fibrillin 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20529844 731578 Fbn1 fibrillin 1 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:1451140 731578 Fbn1 fibrillin 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:7721853 731578 Fbn1 fibrillin 1 gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15254584 731578 Fbn1 fibrillin 1 gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20529844 731578 Fbn1 fibrillin 1 gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21152435 731578 Fbn1 fibrillin 1 gene MP:0003652 abnormal skin turgor IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0003705 abnormal hypodermis morphology IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0003705 abnormal hypodermis morphology IAGP N RGD:5509061 20141003 MGI PMID:4048170 731578 Fbn1 fibrillin 1 gene MP:0003705 abnormal hypodermis morphology IAGP N RGD:5509061 20141003 MGI PMID:7359004 731578 Fbn1 fibrillin 1 gene MP:0003705 abnormal hypodermis morphology IAGP N RGD:5509061 20141003 MGI PMID:7704626 731578 Fbn1 fibrillin 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:11168809 731578 Fbn1 fibrillin 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:7523551 731578 Fbn1 fibrillin 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:7688852 731578 Fbn1 fibrillin 1 gene MP:0003905 abnormal aorta elastin content IAGP N RGD:5509061 20141003 MGI PMID:10931876 731578 Fbn1 fibrillin 1 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:8070538 731578 Fbn1 fibrillin 1 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20200402 MGI PMID:29106398 731578 Fbn1 fibrillin 1 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12485443 731578 Fbn1 fibrillin 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9326947 731578 Fbn1 fibrillin 1 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:22374917 731578 Fbn1 fibrillin 1 gene MP:0004044 aortic dissection IAGP N RGD:5509061 20141003 MGI PMID:15546004 731578 Fbn1 fibrillin 1 gene MP:0004044 aortic dissection IAGP N RGD:5509061 20141003 MGI PMID:9326947 731578 Fbn1 fibrillin 1 gene MP:0004127 thick hypodermis IAGP N RGD:5509061 20141003 MGI PMID:7359004 731578 Fbn1 fibrillin 1 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:22242013 731578 Fbn1 fibrillin 1 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:22242013 731578 Fbn1 fibrillin 1 gene MP:0004389 abnormal respiratory bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:21152435 731578 Fbn1 fibrillin 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0004593 long mandible IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:22242013 731578 Fbn1 fibrillin 1 gene MP:0004671 long ribs IAGP N RGD:5509061 20141003 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0004671 long ribs IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:22242013 731578 Fbn1 fibrillin 1 gene MP:0004695 increased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0004695 increased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0004707 enlarged lumbar vertebrae IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0004735 enlarged thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20200402 MGI PMID:29106398 731578 Fbn1 fibrillin 1 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20200402 MGI PMID:29106398 731578 Fbn1 fibrillin 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20230601 MGI 731578 Fbn1 fibrillin 1 gene MP:0005081 abnormal dermis reticular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10931876 731578 Fbn1 fibrillin 1 gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7704626 731578 Fbn1 fibrillin 1 gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:21152435 731578 Fbn1 fibrillin 1 gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:22374917 731578 Fbn1 fibrillin 1 gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:9326947 731578 Fbn1 fibrillin 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:22374917 731578 Fbn1 fibrillin 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:9326947 731578 Fbn1 fibrillin 1 gene MP:0005275 abnormal skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:11168809 731578 Fbn1 fibrillin 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:2416757 731578 Fbn1 fibrillin 1 gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:20529844 731578 Fbn1 fibrillin 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15254584 731578 Fbn1 fibrillin 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21152435 731578 Fbn1 fibrillin 1 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:6604585 731578 Fbn1 fibrillin 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200402 MGI PMID:29106398 731578 Fbn1 fibrillin 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20200402 MGI PMID:29106398 731578 Fbn1 fibrillin 1 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:12598898 731578 Fbn1 fibrillin 1 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:18339630 731578 Fbn1 fibrillin 1 gene MP:0006045 mitral valve regurgitation IAGP N RGD:5509061 20231221 MGI PMID:15546004 731578 Fbn1 fibrillin 1 gene MP:0006120 mitral valve prolapse IAGP N RGD:5509061 20141003 MGI PMID:15546004 731578 Fbn1 fibrillin 1 gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:22772368 731578 Fbn1 fibrillin 1 gene MP:0006432 abnormal costal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0008054 abnormal uterine NK cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1617705 731578 Fbn1 fibrillin 1 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0008419 abnormal cutaneous microfibril morphology IAGP N RGD:5509061 20141003 MGI PMID:20529844 731578 Fbn1 fibrillin 1 gene MP:0008419 abnormal cutaneous microfibril morphology IAGP N RGD:5509061 20141003 MGI PMID:9490728 731578 Fbn1 fibrillin 1 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:11168809 731578 Fbn1 fibrillin 1 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:10486156 731578 Fbn1 fibrillin 1 gene MP:0008711 increased interleukin-9 secretion IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0008726 increased heart left atrium size IAGP N RGD:5509061 20231221 MGI PMID:15546004 731578 Fbn1 fibrillin 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22242013 731578 Fbn1 fibrillin 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:22374917 731578 Fbn1 fibrillin 1 gene MP:0009545 abnormal dermis papillary layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7359004 731578 Fbn1 fibrillin 1 gene MP:0009826 abnormal dermis reticular layer collagen network IAGP N RGD:5509061 20141003 MGI PMID:10931876 731578 Fbn1 fibrillin 1 gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:15254584 731578 Fbn1 fibrillin 1 gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:22772368 731578 Fbn1 fibrillin 1 gene MP:0009871 abnormal aorta tunica adventitia morphology IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0009871 abnormal aorta tunica adventitia morphology IAGP N RGD:5509061 20141003 MGI PMID:1576433 731578 Fbn1 fibrillin 1 gene MP:0009872 abnormal aorta tunica intima morphology IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:21152435 731578 Fbn1 fibrillin 1 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11168809 731578 Fbn1 fibrillin 1 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:7704626 731578 Fbn1 fibrillin 1 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:7783425 731578 Fbn1 fibrillin 1 gene MP:0010139 aortitis IAGP N RGD:5509061 20141003 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:1433576 731578 Fbn1 fibrillin 1 gene MP:0010470 dilated ascending aorta IAGP N RGD:5509061 20141003 MGI PMID:22374917 731578 Fbn1 fibrillin 1 gene MP:0010483 aortic sinus aneurysm IAGP N RGD:5509061 20141003 MGI PMID:9326947 731578 Fbn1 fibrillin 1 gene MP:0010522 calcified aorta IAGP N RGD:5509061 20201112 MGI PMID:10097121 731578 Fbn1 fibrillin 1 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20231221 MGI PMID:15546004 731578 Fbn1 fibrillin 1 gene MP:0010614 abnormal mitral valve cusp morphology IAGP N RGD:5509061 20231221 MGI PMID:15546004 731578 Fbn1 fibrillin 1 gene MP:0010661 ascending aorta aneurysm IAGP N RGD:5509061 20210617 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:22374917 731578 Fbn1 fibrillin 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:22374917 731578 Fbn1 fibrillin 1 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:22374917 731578 Fbn1 fibrillin 1 gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:6971670 731578 Fbn1 fibrillin 1 gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:7271067 731578 Fbn1 fibrillin 1 gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20141003 MGI PMID:12598898 731578 Fbn1 fibrillin 1 gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20141003 MGI PMID:1587342 731578 Fbn1 fibrillin 1 gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20141003 MGI PMID:18339630 731578 Fbn1 fibrillin 1 gene MP:0010904 abnormal alveolar pore morphology IAGP N RGD:5509061 20141003 MGI PMID:6971670 731578 Fbn1 fibrillin 1 gene MP:0010904 abnormal alveolar pore morphology IAGP N RGD:5509061 20141003 MGI PMID:7271067 731578 Fbn1 fibrillin 1 gene MP:0010908 dilated pulmonary alveolar duct IAGP N RGD:5509061 20141003 MGI PMID:6562869 731578 Fbn1 fibrillin 1 gene MP:0010908 dilated pulmonary alveolar duct IAGP N RGD:5509061 20141003 MGI PMID:6971670 731578 Fbn1 fibrillin 1 gene MP:0010915 increased solitary pulmonary neuroendocrine cell number IAGP N RGD:5509061 20141003 MGI PMID:18339630 731578 Fbn1 fibrillin 1 gene MP:0010918 abnormal pulmonary neuroendocrine body morphology IAGP N RGD:5509061 20141003 MGI PMID:18339630 731578 Fbn1 fibrillin 1 gene MP:0010919 increased number of pulmonary neuroendocrine bodies IAGP N RGD:5509061 20141003 MGI PMID:18339630 731578 Fbn1 fibrillin 1 gene MP:0010922 alveolitis IAGP N RGD:5509061 20141003 MGI PMID:6562869 731578 Fbn1 fibrillin 1 gene MP:0010922 alveolitis IAGP N RGD:5509061 20141003 MGI PMID:6971670 731578 Fbn1 fibrillin 1 gene MP:0010922 alveolitis IAGP N RGD:5509061 20141003 MGI PMID:7271067 731578 Fbn1 fibrillin 1 gene MP:0010937 increased total lung capacity IAGP N RGD:5509061 20141003 MGI PMID:6971670 731578 Fbn1 fibrillin 1 gene MP:0010937 increased total lung capacity IAGP N RGD:5509061 20141003 MGI PMID:7271067 731578 Fbn1 fibrillin 1 gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20141003 MGI PMID:15546004 731578 Fbn1 fibrillin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12598898 731578 Fbn1 fibrillin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15254584 731578 Fbn1 fibrillin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15546004 731578 Fbn1 fibrillin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20529844 731578 Fbn1 fibrillin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21152435 731578 Fbn1 fibrillin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22374917 731578 Fbn1 fibrillin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9326947 731578 Fbn1 fibrillin 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20529844 731578 Fbn1 fibrillin 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24107997 731578 Fbn1 fibrillin 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21152435 731578 Fbn1 fibrillin 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20529844 731578 Fbn1 fibrillin 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21152435 731578 Fbn1 fibrillin 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 731578 Fbn1 fibrillin 1 gene MP:0011575 dilated aorta bulb IAGP N RGD:5509061 20141003 MGI PMID:22772368 731578 Fbn1 fibrillin 1 gene MP:0011696 absent mast cells IAGP N RGD:5509061 20141003 MGI PMID:7704626 731578 Fbn1 fibrillin 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20200402 MGI PMID:29106398 731578 Fbn1 fibrillin 1 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20200402 MGI PMID:29106398 731578 Fbn1 fibrillin 1 gene MP:0014274 decreased respiration IAGP N RGD:5509061 20230810 MGI PMID:16407178 731578 Fbn1 fibrillin 1 gene MP:0014474 decreased pulmonary alveolus wall thickness IAGP N RGD:5509061 20240704 MGI PMID:6971670 731578 Fbn1 fibrillin 1 gene MP:0030799 abnormal tendon sheath morphology IAGP N RGD:5509061 20181011 MGI PMID:176891 731578 Fbn1 fibrillin 1 gene MP:0031157 abnormal arterial thrombosis IAGP N RGD:5509061 20201210 MGI PMID:9326947 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0000603 pale liver IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0000611 jaundice IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0001263 weight loss IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20210422 MGI PMID:33177714 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0002083 premature death IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12920113 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0003326 liver failure IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0005283 increased unsaturated fatty acids level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0010330 abnormal circulating lipoprotein level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0010332 abnormal circulating apolipoprotein level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20151015 MGI PMID:12920113 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0020253 increased collagen level IAGP N RGD:5509061 20151112 MGI PMID:22701022 731580 Hmgcr 3-hydroxy-3-methylglutaryl-Coenzyme A reductase gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:22701022 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20160929 MGI PMID:27534441 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:14697676 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:11087877 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:14697676 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11087877 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11087877 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:11087877 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:14697676 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160929 MGI PMID:27534441 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11087877 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:11087877 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:14697676 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:14697676 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:11087877 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11087877 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:14697676 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11087877 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11087877 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0004831 long incisors IAGP N RGD:5509061 20141003 MGI PMID:14697676 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20240523 MGI 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:14697676 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:14697676 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:14697676 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:14697676 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11087877 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11087877 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14697676 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11087877 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14697676 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 731582 Lpar1 lysophosphatidic acid receptor 1 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20160929 MGI PMID:27534441 731584 Thpo thrombopoietin gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20210826 MGI 731584 Thpo thrombopoietin gene MP:0001314 cornea opacity IEA N RGD:5509061 20220811 MGI 731584 Thpo thrombopoietin gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:8627177 731584 Thpo thrombopoietin gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21262827 731584 Thpo thrombopoietin gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:8627177 731584 Thpo thrombopoietin gene MP:0005573 increased pulmonary respiratory rate IEA N RGD:5509061 20201022 MGI 731584 Thpo thrombopoietin gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 731584 Thpo thrombopoietin gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:21262827 731584 Thpo thrombopoietin gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141211 MGI PMID:24633240 731584 Thpo thrombopoietin gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8627177 731584 Thpo thrombopoietin gene MP:0012125 decreased bronchoconstrictive response IEA N RGD:5509061 20201022 MGI 731587 Sardh sarcosine dehydrogenase gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20210422 MGI PMID:31815201 731587 Sardh sarcosine dehydrogenase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210422 MGI PMID:31815201 731587 Sardh sarcosine dehydrogenase gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20210422 MGI PMID:31815201 731587 Sardh sarcosine dehydrogenase gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20210422 MGI PMID:31815201 731590 Snap29 synaptosomal-associated protein 29 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20160804 MGI 731590 Snap29 synaptosomal-associated protein 29 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0001192 scaly skin IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0001198 tight skin IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 731590 Snap29 synaptosomal-associated protein 29 gene MP:0001874 acanthosis IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160804 MGI 731590 Snap29 synaptosomal-associated protein 29 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0009605 decreased keratohyalin granule number IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0009608 abnormal epidermal lamellar body morphology IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20170309 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20160804 MGI 731590 Snap29 synaptosomal-associated protein 29 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0020352 abnormal endoplasmic reticulum physiology IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20161229 MGI PMID:26747696 731590 Snap29 synaptosomal-associated protein 29 gene MP:0030605 abnormal corneocyte morphology IAGP N RGD:5509061 20180628 MGI PMID:26747696 731592 Pls3 plastin 3 (T-isoform) gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20240404 MGI PMID:37751738 731592 Pls3 plastin 3 (T-isoform) gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20240404 MGI PMID:37751738 731592 Pls3 plastin 3 (T-isoform) gene MP:0000066 osteoporosis IAGP N RGD:5509061 20181227 MGI PMID:30204862 731592 Pls3 plastin 3 (T-isoform) gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20240404 MGI PMID:37751738 731592 Pls3 plastin 3 (T-isoform) gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20240404 MGI PMID:37751738 731592 Pls3 plastin 3 (T-isoform) gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20181227 MGI PMID:30204862 731592 Pls3 plastin 3 (T-isoform) gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 731592 Pls3 plastin 3 (T-isoform) gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 731592 Pls3 plastin 3 (T-isoform) gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20240404 MGI PMID:37751738 731592 Pls3 plastin 3 (T-isoform) gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 731592 Pls3 plastin 3 (T-isoform) gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20240404 MGI PMID:37751738 731592 Pls3 plastin 3 (T-isoform) gene MP:0003385 abnormal body wall morphology IAGP N RGD:5509061 20240404 MGI PMID:37751738 731592 Pls3 plastin 3 (T-isoform) gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20240404 MGI PMID:37751738 731592 Pls3 plastin 3 (T-isoform) gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20181227 MGI PMID:30204862 731592 Pls3 plastin 3 (T-isoform) gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20181227 MGI PMID:30204862 731592 Pls3 plastin 3 (T-isoform) gene MP:0005376 homeostasis/metabolism phenotype IAGP N RGD:5509061 20240404 MGI PMID:37751738 731592 Pls3 plastin 3 (T-isoform) gene MP:0005388 respiratory system phenotype IAGP N RGD:5509061 20240404 MGI PMID:37751738 731592 Pls3 plastin 3 (T-isoform) gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 731592 Pls3 plastin 3 (T-isoform) gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 731592 Pls3 plastin 3 (T-isoform) gene MP:0010770 preweaning lethality IAGP N RGD:5509061 20240404 MGI PMID:37751738 731592 Pls3 plastin 3 (T-isoform) gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20181227 MGI PMID:30204862 731592 Pls3 plastin 3 (T-isoform) gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20181227 MGI PMID:30204862 731592 Pls3 plastin 3 (T-isoform) gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20181227 MGI PMID:30204862 731592 Pls3 plastin 3 (T-isoform) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20240404 MGI PMID:37751738 731592 Pls3 plastin 3 (T-isoform) gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20240404 MGI PMID:37751738 731592 Pls3 plastin 3 (T-isoform) gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20240404 MGI PMID:37751738 731592 Pls3 plastin 3 (T-isoform) gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20181227 MGI PMID:30204862 731592 Pls3 plastin 3 (T-isoform) gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20181227 MGI PMID:30204862 731592 Pls3 plastin 3 (T-isoform) gene MP:0013639 decreased bone stiffness IAGP N RGD:5509061 20181227 MGI PMID:30204862 731592 Pls3 plastin 3 (T-isoform) gene MP:0013857 abnormal abdominal muscle morphology IAGP N RGD:5509061 20240404 MGI PMID:37751738 731595 Atic 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20230810 MGI PMID:36073366 731595 Atic 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20230810 MGI PMID:36073366 731595 Atic 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20230810 MGI PMID:36073366 731595 Atic 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20230810 MGI PMID:36073366 731595 Atic 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20230810 MGI PMID:36073366 731595 Atic 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase gene MP:0031509 decreased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:36073366 731597 Rnf103 ring finger protein 103 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18958194 731597 Rnf103 ring finger protein 103 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18958194 731597 Rnf103 ring finger protein 103 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18958194 731597 Rnf103 ring finger protein 103 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:18958194 731597 Rnf103 ring finger protein 103 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18958194 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:18501887 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18501887 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:21185281 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11784028 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:20737509 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:20386744 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:11784028 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000296 absent trabeculae carneae IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23449628 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:23449628 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20170921 MGI PMID:19341725 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10804186 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:20386744 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:20386744 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18501887 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001026 abnormal adrenergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17531968 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17075884 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:17075884 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17075884 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001435 absent suckling reflex IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:17531968 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:18501887 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11784028 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:10804186 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:9671575 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18501887 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20737509 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9671575 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:10804186 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18501887 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:20737509 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:17531968 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21185281 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:21185281 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:21185281 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:21185281 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:20386744 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:23449628 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:11784028 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003228 abnormal sinus venosus morphology IAGP N RGD:5509061 20141003 MGI PMID:11784028 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:21185281 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20171109 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003808 increased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003854 abnormal forelimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:20386744 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:20386744 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003872 absent heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9671575 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20141003 MGI PMID:9671575 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20386744 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9671575 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23449628 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:20737509 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:11784028 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:17531968 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20386744 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21185281 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9671575 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:11784028 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:21185281 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:11784028 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:9671575 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:20386744 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:20386744 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:20386744 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0009744 postaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:20386744 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0009874 abnormal interdigital cell death IAGP N RGD:5509061 20141003 MGI PMID:20386744 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:19341725 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:19341725 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:19341725 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:17531968 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:18501887 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:19341725 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19341725 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18501887 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0010017 visceral vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:17531968 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0010017 visceral vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0010355 abnormal first pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:21185281 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21185281 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0010457 pulmonary artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0010580 decreased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:21185281 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17531968 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11784028 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17531968 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18501887 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19211672 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21185281 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9671575 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19008477 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21185281 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:10804186 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0012511 dilated aortic sac IAGP N RGD:5509061 20141003 MGI PMID:20386744 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0012511 dilated aortic sac IAGP N RGD:5509061 20141003 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0013164 abnormal forelimb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:10804186 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0013166 small forelimb buds IAGP N RGD:5509061 20141003 MGI PMID:10804186 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:20386744 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0021212 abnormal primary and secondary palatal fusion IAGP N RGD:5509061 20230302 MGI PMID:17531968 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0030339 absent second pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:9171826 731604 Hand2 heart and neural crest derivatives expressed 2 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:19341725 731610 Suclg1 succinate-CoA ligase, GDP-forming, alpha subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731610 Suclg1 succinate-CoA ligase, GDP-forming, alpha subunit gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 731612 Capn9 calpain 9 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:20686710 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0001148 enlarged testis IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0001488 increased startle reflex IEA N RGD:5509061 20231207 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19683723 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0001691 abnormal somite shape IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19683723 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19683723 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19683723 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0003425 abnormal optic vesicle formation IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:19683723 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:19683723 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19683723 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19683723 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19683723 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20231207 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160818 MGI PMID:27064541 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20230601 MGI 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0014181 abnormal respiratory epithelial sodium ion transmembrane transport IAGP N RGD:5509061 20160818 MGI PMID:27064541 731614 Atp1b1 ATPase, Na+/K+ transporting, beta 1 polypeptide gene MP:0014525 impaired pulmonary alveolar fluid clearance IAGP N RGD:5509061 20240912 MGI PMID:27064541 731615 Rims3 regulating synaptic membrane exocytosis 3 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20210128 MGI 731617 Grin3b glutamate receptor, ionotropic, NMDA3B gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:17880385 731617 Grin3b glutamate receptor, ionotropic, NMDA3B gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17880385 731617 Grin3b glutamate receptor, ionotropic, NMDA3B gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17880385 731617 Grin3b glutamate receptor, ionotropic, NMDA3B gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17880385 731617 Grin3b glutamate receptor, ionotropic, NMDA3B gene MP:0001406 abnormal gait IEA N RGD:5509061 20190502 MGI 731617 Grin3b glutamate receptor, ionotropic, NMDA3B gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17880385 731617 Grin3b glutamate receptor, ionotropic, NMDA3B gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:17880385 731617 Grin3b glutamate receptor, ionotropic, NMDA3B gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20220519 MGI 731617 Grin3b glutamate receptor, ionotropic, NMDA3B gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220519 MGI 731617 Grin3b glutamate receptor, ionotropic, NMDA3B gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20220519 MGI 731617 Grin3b glutamate receptor, ionotropic, NMDA3B gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17880385 731617 Grin3b glutamate receptor, ionotropic, NMDA3B gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20220519 MGI 731619 Camk1 calcium/calmodulin-dependent protein kinase I gene MP:0000745 tremors IEA N RGD:5509061 20190502 MGI 731619 Camk1 calcium/calmodulin-dependent protein kinase I gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20201022 MGI 731619 Camk1 calcium/calmodulin-dependent protein kinase I gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 731619 Camk1 calcium/calmodulin-dependent protein kinase I gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 731619 Camk1 calcium/calmodulin-dependent protein kinase I gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 731620 C3ar1 complement component 3a receptor 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12421977 731620 C3ar1 complement component 3a receptor 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:15383607 731620 C3ar1 complement component 3a receptor 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:11067891 731620 C3ar1 complement component 3a receptor 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 731620 C3ar1 complement component 3a receptor 1 gene MP:0002281 abnormal respiratory mucosa goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12421977 731620 C3ar1 complement component 3a receptor 1 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:10984054 731620 C3ar1 complement component 3a receptor 1 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:12421977 731620 C3ar1 complement component 3a receptor 1 gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:12421977 731620 C3ar1 complement component 3a receptor 1 gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20141003 MGI PMID:12421977 731620 C3ar1 complement component 3a receptor 1 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12421977 731620 C3ar1 complement component 3a receptor 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20200109 MGI PMID:23074214 731620 C3ar1 complement component 3a receptor 1 gene MP:0003959 abnormal lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19270708 731620 C3ar1 complement component 3a receptor 1 gene MP:0003981 decreased circulating phospholipid level IAGP N RGD:5509061 20200109 MGI PMID:23074214 731620 C3ar1 complement component 3a receptor 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:15383607 731620 C3ar1 complement component 3a receptor 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:20709903 731620 C3ar1 complement component 3a receptor 1 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12421977 731620 C3ar1 complement component 3a receptor 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12421977 731620 C3ar1 complement component 3a receptor 1 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:19414808 731620 C3ar1 complement component 3a receptor 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20200109 MGI PMID:23074214 731620 C3ar1 complement component 3a receptor 1 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:19270708 731620 C3ar1 complement component 3a receptor 1 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:12421977 731620 C3ar1 complement component 3a receptor 1 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:15240660 731620 C3ar1 complement component 3a receptor 1 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:12421977 731620 C3ar1 complement component 3a receptor 1 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20200109 MGI PMID:23074214 731620 C3ar1 complement component 3a receptor 1 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20200109 MGI PMID:23074214 731620 C3ar1 complement component 3a receptor 1 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12421977 731620 C3ar1 complement component 3a receptor 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12421977 731620 C3ar1 complement component 3a receptor 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200109 MGI PMID:23074214 731620 C3ar1 complement component 3a receptor 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200109 MGI PMID:23074214 731620 C3ar1 complement component 3a receptor 1 gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20200109 MGI PMID:23074214 731620 C3ar1 complement component 3a receptor 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20181227 MGI 731620 C3ar1 complement component 3a receptor 1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20709903 731620 C3ar1 complement component 3a receptor 1 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:11067891 731620 C3ar1 complement component 3a receptor 1 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:15383607 731620 C3ar1 complement component 3a receptor 1 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:12421977 731620 C3ar1 complement component 3a receptor 1 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:12421977 731620 C3ar1 complement component 3a receptor 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:11067891 731620 C3ar1 complement component 3a receptor 1 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:12421977 731620 C3ar1 complement component 3a receptor 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11067891 731620 C3ar1 complement component 3a receptor 1 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200109 MGI PMID:23074214 731620 C3ar1 complement component 3a receptor 1 gene MP:0012040 abnormal c-wave shape IAGP N RGD:5509061 20200109 MGI PMID:23074214 731620 C3ar1 complement component 3a receptor 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200109 MGI PMID:23074214 731620 C3ar1 complement component 3a receptor 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200109 MGI PMID:23074214 731620 C3ar1 complement component 3a receptor 1 gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20200109 MGI PMID:23074214 731620 C3ar1 complement component 3a receptor 1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20200109 MGI PMID:23074214 731620 C3ar1 complement component 3a receptor 1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:23074214 731624 Pola2 polymerase (DNA directed), alpha 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731624 Pola2 polymerase (DNA directed), alpha 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 731624 Pola2 polymerase (DNA directed), alpha 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 731626 Anxa7 annexin A7 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:14608035 731626 Anxa7 annexin A7 gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:14608035 731626 Anxa7 annexin A7 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:10570150 731626 Anxa7 annexin A7 gene MP:0001727 abnormal embryo implantation IAGP N RGD:5509061 20210729 MGI PMID:32923441 731626 Anxa7 annexin A7 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10570150 731626 Anxa7 annexin A7 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11390641 731626 Anxa7 annexin A7 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14644162 731626 Anxa7 annexin A7 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:10570150 731626 Anxa7 annexin A7 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10570150 731626 Anxa7 annexin A7 gene MP:0001934 increased litter size IAGP N RGD:5509061 20210729 MGI PMID:32923441 731626 Anxa7 annexin A7 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14608035 731626 Anxa7 annexin A7 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12925238 731626 Anxa7 annexin A7 gene MP:0002865 increased growth rate IAGP N RGD:5509061 20141003 MGI PMID:14608035 731626 Anxa7 annexin A7 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:10570150 731626 Anxa7 annexin A7 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14608035 731626 Anxa7 annexin A7 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10570150 731626 Anxa7 annexin A7 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:14608035 731626 Anxa7 annexin A7 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10570150 731626 Anxa7 annexin A7 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10570150 731626 Anxa7 annexin A7 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:12925238 731626 Anxa7 annexin A7 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:14644162 731626 Anxa7 annexin A7 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:10570150 731626 Anxa7 annexin A7 gene MP:0009548 abnormal platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:12925238 731626 Anxa7 annexin A7 gene MP:0009662 abnormal uterine receptivity IAGP N RGD:5509061 20210729 MGI PMID:32923441 731626 Anxa7 annexin A7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10570150 731626 Anxa7 annexin A7 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14608035 731627 Dcx doublecortin gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:16387639 731627 Dcx doublecortin gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16387639 731627 Dcx doublecortin gene MP:0000801 abnormal temporal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:12196578 731627 Dcx doublecortin gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:19342486 731627 Dcx doublecortin gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:19342486 731627 Dcx doublecortin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12196578 731627 Dcx doublecortin gene MP:0001462 abnormal avoidance learning behavior IAGP N RGD:5509061 20141003 MGI PMID:12196578 731627 Dcx doublecortin gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12196578 731627 Dcx doublecortin gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12196578 731627 Dcx doublecortin gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 731627 Dcx doublecortin gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12196578 731627 Dcx doublecortin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19342486 731627 Dcx doublecortin gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:16387639 731627 Dcx doublecortin gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16387639 731627 Dcx doublecortin gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19342486 731627 Dcx doublecortin gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16387639 731627 Dcx doublecortin gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19342486 731627 Dcx doublecortin gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 731627 Dcx doublecortin gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:23575857 731627 Dcx doublecortin gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19342486 731627 Dcx doublecortin gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16571605 731627 Dcx doublecortin gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19342486 731627 Dcx doublecortin gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:16571605 731627 Dcx doublecortin gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:12196578 731627 Dcx doublecortin gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 731627 Dcx doublecortin gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0006300 abnormal entorhinal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0008129 absent brain internal capsule IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0008221 abnormal hippocampal commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:16387639 731627 Dcx doublecortin gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16387639 731627 Dcx doublecortin gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:16387639 731627 Dcx doublecortin gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:16387639 731627 Dcx doublecortin gene MP:0008262 abnormal hippocampus region morphology IAGP N RGD:5509061 20141003 MGI PMID:19342486 731627 Dcx doublecortin gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:19342486 731627 Dcx doublecortin gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:19342486 731627 Dcx doublecortin gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:12196578 731627 Dcx doublecortin gene MP:0008285 abnormal hippocampus granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:19342486 731627 Dcx doublecortin gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19342486 731627 Dcx doublecortin gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:12196578 731627 Dcx doublecortin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16387639 731627 Dcx doublecortin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12196578 731627 Dcx doublecortin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16387638 731627 Dcx doublecortin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19342486 731630 Alox8 arachidonate 8-lipoxygenase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190926 MGI PMID:31013822 731630 Alox8 arachidonate 8-lipoxygenase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190926 MGI PMID:31013822 731630 Alox8 arachidonate 8-lipoxygenase gene MP:0001861 lung inflammation IAGP N RGD:5509061 20190926 MGI PMID:31013822 731630 Alox8 arachidonate 8-lipoxygenase gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20190926 MGI PMID:31013822 731630 Alox8 arachidonate 8-lipoxygenase gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20190926 MGI PMID:31013822 731630 Alox8 arachidonate 8-lipoxygenase gene MP:0010857 pulmonary necrosis IAGP N RGD:5509061 20190926 MGI PMID:31013822 731630 Alox8 arachidonate 8-lipoxygenase gene MP:0020945 abnormal susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:31013822 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10092806 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:18393392 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:18393392 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:12556419 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:21436282 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:12556419 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:21436282 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:16901715 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0002425 abnormal susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12556419 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0002933 joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:18490777 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21436282 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:12556419 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16901715 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12556419 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12556419 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12556419 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:19251650 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:19251650 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:18393392 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19251650 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19251650 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21436282 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12556419 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16901715 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20141003 MGI PMID:12556419 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21436282 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0005673 decreased susceptibility to graft versus host disease IAGP N RGD:5509061 20141003 MGI PMID:18490777 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20201119 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19251650 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19251650 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008247 abnormal mononuclear cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19251650 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:16901715 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21436282 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12556419 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21436282 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:12556419 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21436282 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:10092806 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:11452127 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:10092806 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:12556419 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:12556419 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:16901715 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:10092806 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:21436282 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0009322 increased splenocyte apoptosis IAGP N RGD:5509061 20201119 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0009396 small endometrial glands IAGP N RGD:5509061 20150326 MGI PMID:18393392 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:15130911 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10092806 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0009853 decreased Sertoli cell phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:18159085 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20141003 MGI 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20150219 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20201119 MGI PMID:10227296 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:21436282 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201001 MGI PMID:15130911 731632 Mertk MER proto-oncogene tyrosine kinase gene MP:0031168 abnormal brain thrombosis IAGP N RGD:5509061 20201119 MGI PMID:11452127 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:18833191 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:18833191 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0003016 increased circulating bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0003028 alkalosis IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0004119 hypokalemia IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20141003 MGI PMID:18833191 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0004364 thin stria vascularis IAGP N RGD:5509061 20141003 MGI PMID:18833191 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18833191 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:18833191 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:18833191 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0005634 decreased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:18833191 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21593186 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0011039 abnormal vestibuloocular dark reflex IAGP N RGD:5509061 20141003 MGI PMID:18833191 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18833191 731636 Bsnd barttin CLCNK type accessory beta subunit gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18833191 731639 Kcnd1 potassium voltage-gated channel, Shal-related family, member 1 gene MP:0005630 increased lung weight IEA N RGD:5509061 20220811 MGI 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15060135 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21262837 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:21262837 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:19794149 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17550782 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9822608 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170406 MGI PMID:18846252 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15060135 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19794149 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9822608 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180531 MGI PMID:28178239 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:17550782 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:11140689 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15060135 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0001661 extended life span IAGP N RGD:5509061 20180531 MGI PMID:28178239 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15060135 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15060135 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9822608 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15060135 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15060135 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21262837 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:17550782 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:15060135 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11140689 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20170406 MGI PMID:18846252 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20170406 MGI PMID:18846252 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:11140689 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:19794149 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20170406 MGI PMID:18846252 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:15060135 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20170406 MGI PMID:18846252 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20180531 MGI PMID:28178239 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11140689 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20170406 MGI PMID:18846252 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:17550782 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20180531 MGI PMID:28178239 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:11140689 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20170406 MGI PMID:18846252 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:11140689 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20180531 MGI PMID:28178239 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20180531 MGI PMID:28178239 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20180531 MGI PMID:28178239 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20180531 MGI PMID:28178239 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20180531 MGI PMID:28178239 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:17550782 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:19794149 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21262837 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20150611 MGI PMID:17550782 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:17550782 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15060135 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15060135 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15060135 731645 Rps6kb1 ribosomal protein S6 kinase, polypeptide 1 gene MP:0014173 increased fatty acid beta-oxidation IAGP N RGD:5509061 20160421 MGI PMID:17550782 731646 Cd38 CD38 antigen gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 731646 Cd38 CD38 antigen gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 731646 Cd38 CD38 antigen gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 731646 Cd38 CD38 antigen gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 731646 Cd38 CD38 antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:9694721 731646 Cd38 CD38 antigen gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 731646 Cd38 CD38 antigen gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9890936 731646 Cd38 CD38 antigen gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:16585549 731646 Cd38 CD38 antigen gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:16585549 731646 Cd38 CD38 antigen gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:16585549 731646 Cd38 CD38 antigen gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:9890936 731646 Cd38 CD38 antigen gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:17003338 731646 Cd38 CD38 antigen gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:9694721 731646 Cd38 CD38 antigen gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16585549 731646 Cd38 CD38 antigen gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20230119 MGI 731646 Cd38 CD38 antigen gene MP:0008044 increased NK cell number IEA N RGD:5509061 20230119 MGI 731646 Cd38 CD38 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20230119 MGI 731646 Cd38 CD38 antigen gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:17003338 731646 Cd38 CD38 antigen gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:17003338 731646 Cd38 CD38 antigen gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20230119 MGI 731646 Cd38 CD38 antigen gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20230119 MGI 731646 Cd38 CD38 antigen gene MP:0013519 decreased CD4-positive NK T cell number IEA N RGD:5509061 20230119 MGI 731646 Cd38 CD38 antigen gene MP:0013522 decreased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20230119 MGI 731646 Cd38 CD38 antigen gene MP:0013764 decreased T-helper cell number IEA N RGD:5509061 20230119 MGI 731646 Cd38 CD38 antigen gene MP:0013771 decreased effector memory T-helper cell number IEA N RGD:5509061 20230119 MGI 731646 Cd38 CD38 antigen gene MP:0014121 increased pancreatic islet cell apoptosis IAGP N RGD:5509061 20160324 MGI PMID:17003338 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20150723 MGI PMID:24710642 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16215705 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19477223 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150723 MGI PMID:19293327 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150723 MGI PMID:24710642 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150730 MGI PMID:21031341 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001263 weight loss IAGP N RGD:5509061 20150723 MGI PMID:24710642 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001263 weight loss IAGP N RGD:5509061 20150730 MGI PMID:21031341 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001265 decreased body size IAGP N RGD:5509061 20150723 MGI PMID:19293327 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20150730 MGI PMID:18343518 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19477223 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001394 circling IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001410 head bobbing IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20150730 MGI PMID:18343518 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001522 impaired swimming IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001523 impaired righting response IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16215705 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20150730 MGI PMID:21031341 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220609 MGI PMID:19664290 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0001967 deafness IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20150730 MGI PMID:18343518 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16215705 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220609 MGI PMID:19664290 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20150723 MGI PMID:24710642 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0002694 abnormal pancreas secretion IAGP N RGD:5509061 20141003 MGI PMID:15056606 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0002710 increased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:15056606 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15056606 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16215705 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20150730 MGI PMID:21031341 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:19477223 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0002980 abnormal postural reflex IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:16215705 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0003063 increased coping response IAGP N RGD:5509061 20150730 MGI PMID:18343518 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:15056606 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:16215705 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16215705 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20150730 MGI PMID:18343518 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0003999 enhanced passive avoidance behavior IAGP N RGD:5509061 20150730 MGI PMID:18343518 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0004270 analgesia IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0004516 fused vestibular hair cell stereocilia IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0004530 absent outer hair cell stereocilia IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20150723 MGI PMID:24710642 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20150723 MGI PMID:19293327 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220609 MGI PMID:19664290 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:16215705 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20220609 MGI PMID:19664290 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20150723 MGI PMID:24710642 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15056606 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16215705 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20150723 MGI PMID:19293327 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20150730 MGI PMID:21031341 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15056606 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20150730 MGI PMID:21031341 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20150723 MGI PMID:24710642 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0006325 impaired hearing IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20220609 MGI PMID:19664290 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20150730 MGI PMID:21031341 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220609 MGI PMID:19664290 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:16215705 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220609 MGI PMID:19664290 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:16215705 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20150730 MGI PMID:21031341 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220609 MGI PMID:19664290 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0011940 decreased food intake IAGP N RGD:5509061 20150723 MGI PMID:24710642 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20240118 MGI PMID:37386014 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0012294 enhanced active avoidance behavior IAGP N RGD:5509061 20150730 MGI PMID:18343518 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:19041897 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0031426 increased sperm motility IAGP N RGD:5509061 20220714 MGI PMID:19664290 731650 Wfs1 wolframin ER transmembrane glycoprotein gene MP:0031436 decreased copulatory plug deposition IAGP N RGD:5509061 20220922 MGI PMID:19664290 731651 Ctss cathepsin S gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12639996 731651 Ctss cathepsin S gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15944319 731651 Ctss cathepsin S gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20160714 MGI PMID:26966179 731651 Ctss cathepsin S gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19664906 731651 Ctss cathepsin S gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:15661938 731651 Ctss cathepsin S gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15661938 731651 Ctss cathepsin S gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15661938 731651 Ctss cathepsin S gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:19664906 731651 Ctss cathepsin S gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20141003 MGI PMID:15944319 731651 Ctss cathepsin S gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:15944319 731651 Ctss cathepsin S gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15661938 731651 Ctss cathepsin S gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15661938 731651 Ctss cathepsin S gene MP:0002453 abnormal B lymphocyte antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:10072073 731651 Ctss cathepsin S gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15661938 731651 Ctss cathepsin S gene MP:0002608 increased hematocrit IEA N RGD:5509061 20240523 MGI 731651 Ctss cathepsin S gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15661938 731651 Ctss cathepsin S gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20160714 MGI PMID:26966179 731651 Ctss cathepsin S gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:12639996 731651 Ctss cathepsin S gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:10072073 731651 Ctss cathepsin S gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12639996 731651 Ctss cathepsin S gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12600886 731651 Ctss cathepsin S gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:19664906 731651 Ctss cathepsin S gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:19664906 731651 Ctss cathepsin S gene MP:0004824 decreased susceptibility to experimental autoimmune myasthenia gravis IAGP N RGD:5509061 20141003 MGI PMID:15661938 731651 Ctss cathepsin S gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20230119 MGI 731651 Ctss cathepsin S gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15944319 731651 Ctss cathepsin S gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12639996 731651 Ctss cathepsin S gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12639996 731651 Ctss cathepsin S gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:15944319 731651 Ctss cathepsin S gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12600886 731651 Ctss cathepsin S gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15944319 731651 Ctss cathepsin S gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:15661938 731651 Ctss cathepsin S gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20160714 MGI PMID:26966179 731651 Ctss cathepsin S gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20160714 MGI PMID:26966179 731651 Ctss cathepsin S gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20160714 MGI PMID:26966179 731651 Ctss cathepsin S gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20160714 MGI PMID:26966179 731651 Ctss cathepsin S gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:15944319 731651 Ctss cathepsin S gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20160714 MGI PMID:26966179 731651 Ctss cathepsin S gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20190103 MGI 731654 Ppp4r1 protein phosphatase 4, regulatory subunit 1 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20211021 MGI 731654 Ppp4r1 protein phosphatase 4, regulatory subunit 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 731654 Ppp4r1 protein phosphatase 4, regulatory subunit 1 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20211021 MGI 731654 Ppp4r1 protein phosphatase 4, regulatory subunit 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 731658 Vax2 ventral anterior homeobox 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:15905411 731658 Vax2 ventral anterior homeobox 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11830578 731658 Vax2 ventral anterior homeobox 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11830578 731658 Vax2 ventral anterior homeobox 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11830578 731658 Vax2 ventral anterior homeobox 2 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15905411 731658 Vax2 ventral anterior homeobox 2 gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:11830578 731658 Vax2 ventral anterior homeobox 2 gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:15905411 731658 Vax2 ventral anterior homeobox 2 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:11830578 731658 Vax2 ventral anterior homeobox 2 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:15905411 731658 Vax2 ventral anterior homeobox 2 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:11830579 731658 Vax2 ventral anterior homeobox 2 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:15905411 731658 Vax2 ventral anterior homeobox 2 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11830579 731658 Vax2 ventral anterior homeobox 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15905411 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20170831 MGI PMID:26558540 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170831 MGI PMID:26558540 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0002083 premature death IAGP N RGD:5509061 20170831 MGI PMID:26558540 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20170831 MGI PMID:26558540 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20170831 MGI PMID:26558540 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20170831 MGI PMID:26558540 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0005635 decreased circulating bilirubin level IAGP N RGD:5509061 20170831 MGI PMID:26558540 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0008817 hematoma IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170831 MGI PMID:26558540 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21636789 731660 Anp32b acidic nuclear phosphoprotein 32 family member B gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:21636789 731664 Mfn1 mitofusin 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17693261 731664 Mfn1 mitofusin 1 gene MP:0001147 small testis IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17693261 731664 Mfn1 mitofusin 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20240926 MGI PMID:31675497 731664 Mfn1 mitofusin 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:17693261 731664 Mfn1 mitofusin 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:17693261 731664 Mfn1 mitofusin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12527753 731664 Mfn1 mitofusin 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12527753 731664 Mfn1 mitofusin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17693261 731664 Mfn1 mitofusin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22859504 731664 Mfn1 mitofusin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22914740 731664 Mfn1 mitofusin 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20240926 MGI PMID:31675497 731664 Mfn1 mitofusin 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12527753 731664 Mfn1 mitofusin 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0004930 small epididymis IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20240926 MGI PMID:31675497 731664 Mfn1 mitofusin 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:12527753 731664 Mfn1 mitofusin 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:17693261 731664 Mfn1 mitofusin 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:12527753 731664 Mfn1 mitofusin 1 gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:17693261 731664 Mfn1 mitofusin 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:17693261 731664 Mfn1 mitofusin 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17693261 731664 Mfn1 mitofusin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17693261 731664 Mfn1 mitofusin 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17693261 731664 Mfn1 mitofusin 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17693261 731664 Mfn1 mitofusin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 731664 Mfn1 mitofusin 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12527753 731664 Mfn1 mitofusin 1 gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20230413 MGI PMID:33674260 731664 Mfn1 mitofusin 1 gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20230413 MGI PMID:33674260 731665 Anxa3 annexin A3 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20200528 MGI PMID:32020697 731665 Anxa3 annexin A3 gene MP:0010098 abnormal retina blood vessel pattern IAGP N RGD:5509061 20200528 MGI PMID:32020697 731666 Grm8 glutamate receptor, metabotropic 8 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16045496 731666 Grm8 glutamate receptor, metabotropic 8 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 731666 Grm8 glutamate receptor, metabotropic 8 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16045496 731666 Grm8 glutamate receptor, metabotropic 8 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20141003 MGI 731666 Grm8 glutamate receptor, metabotropic 8 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:16045496 731666 Grm8 glutamate receptor, metabotropic 8 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:16045496 731666 Grm8 glutamate receptor, metabotropic 8 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:16045496 731666 Grm8 glutamate receptor, metabotropic 8 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:16045496 731666 Grm8 glutamate receptor, metabotropic 8 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12213276 731666 Grm8 glutamate receptor, metabotropic 8 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20141003 MGI 731667 Akr1c14 aldo-keto reductase family 1, member C14 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20220721 MGI PMID:34400844 731667 Akr1c14 aldo-keto reductase family 1, member C14 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20220721 MGI PMID:34400844 731667 Akr1c14 aldo-keto reductase family 1, member C14 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20220721 MGI PMID:34400844 731667 Akr1c14 aldo-keto reductase family 1, member C14 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20220721 MGI PMID:34400844 731667 Akr1c14 aldo-keto reductase family 1, member C14 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20220721 MGI PMID:34400844 731667 Akr1c14 aldo-keto reductase family 1, member C14 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20220721 MGI PMID:34400844 731667 Akr1c14 aldo-keto reductase family 1, member C14 gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20220721 MGI PMID:34400844 731667 Akr1c14 aldo-keto reductase family 1, member C14 gene MP:0010540 long stride length IAGP N RGD:5509061 20220721 MGI PMID:34400844 731667 Akr1c14 aldo-keto reductase family 1, member C14 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20220721 MGI PMID:34400844 731667 Akr1c14 aldo-keto reductase family 1, member C14 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20220721 MGI PMID:34400844 731668 Caly calcyon neuron-specific vesicular protein gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:19120439 731668 Caly calcyon neuron-specific vesicular protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16595675 731668 Caly calcyon neuron-specific vesicular protein gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:16595675 731668 Caly calcyon neuron-specific vesicular protein gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:19120439 731670 Ppp1cb protein phosphatase 1 catalytic subunit beta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 731672 Ilf3 interleukin enhancer binding factor 3 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:15746098 731672 Ilf3 interleukin enhancer binding factor 3 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15746098 731672 Ilf3 interleukin enhancer binding factor 3 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:15746098 731672 Ilf3 interleukin enhancer binding factor 3 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:15746098 731672 Ilf3 interleukin enhancer binding factor 3 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:15746098 731672 Ilf3 interleukin enhancer binding factor 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15746098 731672 Ilf3 interleukin enhancer binding factor 3 gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15746098 731672 Ilf3 interleukin enhancer binding factor 3 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15746098 731672 Ilf3 interleukin enhancer binding factor 3 gene MP:0005426 tachypnea IAGP N RGD:5509061 20141003 MGI PMID:15746098 731672 Ilf3 interleukin enhancer binding factor 3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15746098 731672 Ilf3 interleukin enhancer binding factor 3 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:15746098 731672 Ilf3 interleukin enhancer binding factor 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15746098 731672 Ilf3 interleukin enhancer binding factor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15746098 731672 Ilf3 interleukin enhancer binding factor 3 gene MP:0020931 increased susceptibility to Adenoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:21123651 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:11555633 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11555633 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11555633 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11555633 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11555633 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11555633 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16816367 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12761045 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0003158 dysphagia IAGP N RGD:5509061 20141003 MGI PMID:11555633 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20141003 MGI PMID:11555633 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12761045 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16816367 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16816367 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12761045 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16816367 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:11555633 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:16816367 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:16816367 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:16816367 731674 Uchl3 ubiquitin carboxyl-terminal esterase L3 (ubiquitin thiolesterase) gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:16816367 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20160519 MGI PMID:22609941 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17320843 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:17320843 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18753375 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20529126 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15677329 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:2289471 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18753375 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20529126 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:2289471 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20529126 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:20529126 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:2289471 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22002768 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:2289471 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22002768 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:8229188 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12151514 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:18753375 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0002623 abnormal vestibular hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:8229188 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20547132 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18753375 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:15677329 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:8229188 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:8229188 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:20529126 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20141003 MGI PMID:17070505 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0004428 abnormal type I vestibular cell IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18753375 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20547132 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20210225 MGI PMID:32697982 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17070505 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:17070505 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:2289471 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:8229188 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:17070505 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:8229188 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:17070505 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:2289471 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20160519 MGI PMID:22609941 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:8229188 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0011001 absence of AMPA-mediated synaptic currents IAGP N RGD:5509061 20240328 MGI PMID:20547132 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18923036 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20529126 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15677329 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18753375 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15677329 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20210225 MGI PMID:32697982 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:20529126 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0011272 short excitatory postsynaptic current rise time IAGP N RGD:5509061 20210225 MGI PMID:32697982 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0011274 short excitatory postsynaptic current decay time IAGP N RGD:5509061 20210225 MGI PMID:32697982 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15283975 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0014372 decreased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:20547132 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0014372 decreased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:32697982 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0014373 increased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:20547132 731677 Cacng2 calcium channel, voltage-dependent, gamma subunit 2 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:32697982 731683 Sort1 sortilin 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17934455 731683 Sort1 sortilin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23091165 731683 Sort1 sortilin 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:23091165 731683 Sort1 sortilin 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17934455 731683 Sort1 sortilin 1 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:19732768 731683 Sort1 sortilin 1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:20133718 731683 Sort1 sortilin 1 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17934455 731683 Sort1 sortilin 1 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:20133718 731683 Sort1 sortilin 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 731684 Cdc25b cell division cycle 25B gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21283624 731684 Cdc25b cell division cycle 25B gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21283624 731684 Cdc25b cell division cycle 25B gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11912493 731684 Cdc25b cell division cycle 25B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21283624 731684 Cdc25b cell division cycle 25B gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19273838 731684 Cdc25b cell division cycle 25B gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:11912493 731684 Cdc25b cell division cycle 25B gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11912493 731684 Cdc25b cell division cycle 25B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19273838 731684 Cdc25b cell division cycle 25B gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:19273838 731684 Cdc25b cell division cycle 25B gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:21283624 731684 Cdc25b cell division cycle 25B gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:11912493 731684 Cdc25b cell division cycle 25B gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:19273838 731684 Cdc25b cell division cycle 25B gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20141003 MGI PMID:21283624 731684 Cdc25b cell division cycle 25B gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21283624 731684 Cdc25b cell division cycle 25B gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21283624 731684 Cdc25b cell division cycle 25B gene MP:0010159 abnormal enterocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:21283624 731684 Cdc25b cell division cycle 25B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21283624 731684 Cdc25b cell division cycle 25B gene MP:0013958 decreased small intestine length IAGP N RGD:5509061 20160310 MGI PMID:19273838 731684 Cdc25b cell division cycle 25B gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20160310 MGI PMID:19273838 731685 Nr2c1 nuclear receptor subfamily 2, group C, member 1 gene MP:0001588 abnormal hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:17431400 731685 Nr2c1 nuclear receptor subfamily 2, group C, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12052874 731686 Cyp3a13 cytochrome P450, family 3, subfamily a, polypeptide 13 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17975676 731686 Cyp3a13 cytochrome P450, family 3, subfamily a, polypeptide 13 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:23125282 731686 Cyp3a13 cytochrome P450, family 3, subfamily a, polypeptide 13 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17975676 731686 Cyp3a13 cytochrome P450, family 3, subfamily a, polypeptide 13 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:17975676 731686 Cyp3a13 cytochrome P450, family 3, subfamily a, polypeptide 13 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17975676 731689 Il1r2 interleukin 1 receptor, type II gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20240613 MGI PMID:38329807 731689 Il1r2 interleukin 1 receptor, type II gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20240613 MGI PMID:38329807 731689 Il1r2 interleukin 1 receptor, type II gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20240613 MGI PMID:38329807 731689 Il1r2 interleukin 1 receptor, type II gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20240613 MGI PMID:25725107 731689 Il1r2 interleukin 1 receptor, type II gene MP:0002493 increased IgG level IAGP N RGD:5509061 20240613 MGI PMID:38329807 731689 Il1r2 interleukin 1 receptor, type II gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20240613 MGI PMID:25725107 731689 Il1r2 interleukin 1 receptor, type II gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 731689 Il1r2 interleukin 1 receptor, type II gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20240613 MGI PMID:38329807 731689 Il1r2 interleukin 1 receptor, type II gene MP:0008077 abnormal CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20240613 MGI PMID:38329807 731689 Il1r2 interleukin 1 receptor, type II gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20240613 MGI PMID:38329807 731689 Il1r2 interleukin 1 receptor, type II gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20240613 MGI PMID:25725107 731689 Il1r2 interleukin 1 receptor, type II gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20240613 MGI PMID:38329807 731689 Il1r2 interleukin 1 receptor, type II gene MP:0008638 increased circulating interleukin-1 alpha level IAGP N RGD:5509061 20240613 MGI PMID:38329807 731689 Il1r2 interleukin 1 receptor, type II gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 731689 Il1r2 interleukin 1 receptor, type II gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20240613 MGI PMID:38329807 731689 Il1r2 interleukin 1 receptor, type II gene MP:0011078 increased macrophage cytokine production IAGP N RGD:5509061 20240613 MGI PMID:25725107 731689 Il1r2 interleukin 1 receptor, type II gene MP:0012763 abnormal alpha-beta T cell number IAGP N RGD:5509061 20240613 MGI PMID:38329807 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15596719 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18165355 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18971423 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20191003 MGI PMID:30675063 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20191003 MGI PMID:30675063 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20211021 MGI 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15596719 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20141003 MGI PMID:15596719 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15596719 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15596719 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18165355 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:11960641 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20211021 MGI 731691 Cx3cl1 C-X3-C motif chemokine ligand 1 gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:16732273 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20240321 MGI PMID:33214341 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20230601 MGI 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230601 MGI 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20240321 MGI PMID:33214341 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20240321 MGI PMID:28602864 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0003064 decreased coping response IAGP N RGD:5509061 20240321 MGI PMID:33214341 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20230601 MGI 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20240523 MGI 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20240321 MGI PMID:28602864 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20240321 MGI PMID:28602864 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20240321 MGI PMID:33807999 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20240321 MGI PMID:33807999 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20231207 MGI 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20240321 MGI PMID:28602864 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20230601 MGI 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0011941 increased fluid intake IEA N RGD:5509061 20230601 MGI 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20240321 MGI PMID:28602864 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20240321 MGI PMID:28602864 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0013639 decreased bone stiffness IAGP N RGD:5509061 20240321 MGI PMID:28602864 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20240321 MGI PMID:33807999 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20240321 MGI PMID:28602864 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20240321 MGI PMID:33214341 731693 Slc24a3 solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20240321 MGI PMID:33214341 731698 Rpl5 ribosomal protein L5 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0000585 kinked tail IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0002083 premature death IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0003051 curly tail IEA N RGD:5509061 20221110 MGI 731698 Rpl5 ribosomal protein L5 gene MP:0003109 short femur IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0003717 pallor IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0010114 abnormal coccyx morphology IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20191024 MGI PMID:26722357 731698 Rpl5 ribosomal protein L5 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20221110 MGI PMID:34464976 731698 Rpl5 ribosomal protein L5 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20221110 MGI PMID:34464976 731701 Cd81 CD81 antigen gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12796480 731701 Cd81 CD81 antigen gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12357429 731701 Cd81 CD81 antigen gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9250665 731701 Cd81 CD81 antigen gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:12357429 731701 Cd81 CD81 antigen gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:12357429 731701 Cd81 CD81 antigen gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:12357429 731701 Cd81 CD81 antigen gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12357429 731701 Cd81 CD81 antigen gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12796480 731701 Cd81 CD81 antigen gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11376857 731701 Cd81 CD81 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:9126932 731701 Cd81 CD81 antigen gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:11376857 731701 Cd81 CD81 antigen gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:12796480 731701 Cd81 CD81 antigen gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12796480 731701 Cd81 CD81 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9250665 731701 Cd81 CD81 antigen gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:12357429 731701 Cd81 CD81 antigen gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12796480 731701 Cd81 CD81 antigen gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12796480 731701 Cd81 CD81 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9380722 731701 Cd81 CD81 antigen gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:9380722 731701 Cd81 CD81 antigen gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12357429 731701 Cd81 CD81 antigen gene MP:0004080 abnormal nucleus accumbens morphology IAGP N RGD:5509061 20141003 MGI PMID:11376857 731701 Cd81 CD81 antigen gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9126932 731701 Cd81 CD81 antigen gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9380722 731701 Cd81 CD81 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:9250665 731701 Cd81 CD81 antigen gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:9380722 731701 Cd81 CD81 antigen gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:12796480 731701 Cd81 CD81 antigen gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:12483205 731701 Cd81 CD81 antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9250665 731701 Cd81 CD81 antigen gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9250665 731701 Cd81 CD81 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9250665 731701 Cd81 CD81 antigen gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9380722 731701 Cd81 CD81 antigen gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:9126932 731701 Cd81 CD81 antigen gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:9482907 731701 Cd81 CD81 antigen gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:9482907 731701 Cd81 CD81 antigen gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:9380722 731701 Cd81 CD81 antigen gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:12357429 731701 Cd81 CD81 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9126932 731701 Cd81 CD81 antigen gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9380722 731701 Cd81 CD81 antigen gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:11376857 731701 Cd81 CD81 antigen gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12357429 731701 Cd81 CD81 antigen gene MP:0012065 increased astrocyte number IAGP N RGD:5509061 20170907 MGI PMID:12357429 731701 Cd81 CD81 antigen gene MP:0020082 increased hippocampus volume IAGP N RGD:5509061 20170706 MGI PMID:12357429 731702 Saxo4 stabilizer of axonemal microtubules 4 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240627 MGI 731702 Saxo4 stabilizer of axonemal microtubules 4 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20231207 MGI 731702 Saxo4 stabilizer of axonemal microtubules 4 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20240627 MGI PMID:38835510 731704 Gpc2 glypican 2 cerebroglycan gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19732411 731704 Gpc2 glypican 2 cerebroglycan gene MP:0002768 small adrenal glands IEA N RGD:5509061 20160811 MGI 731704 Gpc2 glypican 2 cerebroglycan gene MP:0002989 small kidney IEA N RGD:5509061 20160811 MGI 731704 Gpc2 glypican 2 cerebroglycan gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20220519 MGI 731704 Gpc2 glypican 2 cerebroglycan gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20160421 MGI 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:16477021 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:16477021 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:16477021 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16477021 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16477021 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:16477021 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0006326 conductive hearing impairment IAGP N RGD:5509061 20141003 MGI PMID:16477021 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0006336 abnormal otoacoustic response IAGP N RGD:5509061 20141003 MGI PMID:16477021 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:16477021 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:15091340 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16269331 731705 Dnajc5 DnaJ heat shock protein family (Hsp40) member C5 gene MP:0031287 bilateral cryptorchism IAGP N RGD:5509061 20211014 MGI PMID:15091340 731709 Hnrnpf heterogeneous nuclear ribonucleoprotein F gene MP:0000231 hypertension IAGP N RGD:5509061 20200310 MGI PMID:31673025 731709 Hnrnpf heterogeneous nuclear ribonucleoprotein F gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20200310 MGI PMID:31673025 731709 Hnrnpf heterogeneous nuclear ribonucleoprotein F gene MP:0001762 polyuria IAGP N RGD:5509061 20200310 MGI PMID:31673025 731709 Hnrnpf heterogeneous nuclear ribonucleoprotein F gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:31673025 731709 Hnrnpf heterogeneous nuclear ribonucleoprotein F gene MP:0002871 albuminuria IAGP N RGD:5509061 20200310 MGI PMID:31673025 731709 Hnrnpf heterogeneous nuclear ribonucleoprotein F gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20200310 MGI PMID:31673025 731709 Hnrnpf heterogeneous nuclear ribonucleoprotein F gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20200310 MGI PMID:31673025 731709 Hnrnpf heterogeneous nuclear ribonucleoprotein F gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20200310 MGI PMID:31673025 731709 Hnrnpf heterogeneous nuclear ribonucleoprotein F gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20200310 MGI PMID:31673025 731709 Hnrnpf heterogeneous nuclear ribonucleoprotein F gene MP:0031229 increased angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:31673025 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:19841070 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15363411 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19841070 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18292538 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18250339 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0002531 abnormal type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18203950 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0002694 abnormal pancreas secretion IAGP N RGD:5509061 20141003 MGI PMID:18535671 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:19841070 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:19841070 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0004155 decreased susceptibility to induced pancreatitis IAGP N RGD:5509061 20141003 MGI PMID:18535671 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:19841070 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:19841070 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:17065550 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:18535671 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:17065550 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:18203950 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0008804 abnormal circulating amylase level IAGP N RGD:5509061 20141003 MGI PMID:18535671 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:19841070 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15363411 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0009160 abnormal pancreatic acinar cell zymogen granule morphology IAGP N RGD:5509061 20141003 MGI PMID:18535671 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0009161 pancreatic acinar cell zymogen granule accumulation IAGP N RGD:5509061 20141003 MGI PMID:15363411 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:19841070 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15363411 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19841070 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0011413 colorless urine IAGP N RGD:5509061 20141003 MGI PMID:19841070 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0011422 kidney medulla atrophy IAGP N RGD:5509061 20141003 MGI PMID:19841070 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0011885 abnormal circulating lipase level IAGP N RGD:5509061 20150611 MGI PMID:18535671 731713 Vamp8 vesicle-associated membrane protein 8 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:19841070 731721 Ccn1 cellular communication network factor 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:17023674 731721 Ccn1 cellular communication network factor 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:17023674 731721 Ccn1 cellular communication network factor 1 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:17023674 731721 Ccn1 cellular communication network factor 1 gene MP:0000299 failure of atrioventricular cushion closure IAGP N RGD:5509061 20141003 MGI PMID:17023674 731721 Ccn1 cellular communication network factor 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12446788 731721 Ccn1 cellular communication network factor 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:12446788 731721 Ccn1 cellular communication network factor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12446788 731721 Ccn1 cellular communication network factor 1 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12446788 731721 Ccn1 cellular communication network factor 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23508104 731721 Ccn1 cellular communication network factor 1 gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:12446788 731721 Ccn1 cellular communication network factor 1 gene MP:0004225 patent cardiac foramen ovale IAGP N RGD:5509061 20141003 MGI PMID:17023674 731721 Ccn1 cellular communication network factor 1 gene MP:0004266 pale placenta IAGP N RGD:5509061 20141003 MGI PMID:12446788 731721 Ccn1 cellular communication network factor 1 gene MP:0004560 abnormal chorionic plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12446788 731721 Ccn1 cellular communication network factor 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12446788 731721 Ccn1 cellular communication network factor 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:23508104 731721 Ccn1 cellular communication network factor 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17318182 731721 Ccn1 cellular communication network factor 1 gene MP:0008007 abnormal cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:23508104 731721 Ccn1 cellular communication network factor 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12446788 731721 Ccn1 cellular communication network factor 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12446788 731721 Ccn1 cellular communication network factor 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17023674 731721 Ccn1 cellular communication network factor 1 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:17023674 731721 Ccn1 cellular communication network factor 1 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17023674 731721 Ccn1 cellular communication network factor 1 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:17023674 731721 Ccn1 cellular communication network factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12446788 731721 Ccn1 cellular communication network factor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12446788 731727 Myt1l myelin transcription factor 1-like gene MP:0000746 weakness IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0000774 decreased brain size IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0001261 obese IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0001261 obese IAGP N RGD:5509061 20220825 MGI PMID:35538503 731727 Myt1l myelin transcription factor 1-like gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20220825 MGI PMID:35538503 731727 Myt1l myelin transcription factor 1-like gene MP:0001399 hyperactivity IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0001405 impaired coordination IAGP N RGD:5509061 20220825 MGI PMID:35538503 731727 Myt1l myelin transcription factor 1-like gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20220825 MGI PMID:35538503 731727 Myt1l myelin transcription factor 1-like gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20220825 MGI PMID:35538503 731727 Myt1l myelin transcription factor 1-like gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20220825 MGI PMID:35538503 731727 Myt1l myelin transcription factor 1-like gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0006253 clinodactyly IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20220825 MGI PMID:35538503 731727 Myt1l myelin transcription factor 1-like gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0010087 increased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 731727 Myt1l myelin transcription factor 1-like gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20220825 MGI PMID:35538503 731727 Myt1l myelin transcription factor 1-like gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20220825 MGI PMID:35538503 731727 Myt1l myelin transcription factor 1-like gene MP:0013140 excessive vocalization IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0013140 excessive vocalization IAGP N RGD:5509061 20220825 MGI PMID:35538503 731727 Myt1l myelin transcription factor 1-like gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0020507 increased dendritic spine density IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0020512 abnormal dendritic mushroom spine morphology IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0020513 abnormal dendritic stubby spine morphology IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0020514 abnormal dendritic thin spine morphology IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220512 MGI PMID:34614421 731727 Myt1l myelin transcription factor 1-like gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220825 MGI PMID:35538503 731729 Casp1 caspase 1 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:10639148 731729 Casp1 caspase 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12444148 731729 Casp1 caspase 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12444148 731729 Casp1 caspase 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:10899911 731729 Casp1 caspase 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10899911 731729 Casp1 caspase 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16717117 731729 Casp1 caspase 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16861683 731729 Casp1 caspase 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16984919 731729 Casp1 caspase 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18493980 731729 Casp1 caspase 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16429160 731729 Casp1 caspase 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16861683 731729 Casp1 caspase 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18493980 731729 Casp1 caspase 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:7859282 731729 Casp1 caspase 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:12444148 731729 Casp1 caspase 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:7535475 731729 Casp1 caspase 1 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:11298831 731729 Casp1 caspase 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14663141 731729 Casp1 caspase 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:10639148 731729 Casp1 caspase 1 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:11342578 731729 Casp1 caspase 1 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:15644489 731729 Casp1 caspase 1 gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:11342578 731729 Casp1 caspase 1 gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:15644489 731729 Casp1 caspase 1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23090995 731729 Casp1 caspase 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:10452974 731729 Casp1 caspase 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:14645573 731729 Casp1 caspase 1 gene MP:0005376 homeostasis/metabolism phenotype IAGP N RGD:5509061 20200917 MGI PMID:26832955 731729 Casp1 caspase 1 gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20200917 MGI PMID:26832955 731729 Casp1 caspase 1 gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:15644489 731729 Casp1 caspase 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10899911 731729 Casp1 caspase 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20180111 MGI PMID:28636595 731729 Casp1 caspase 1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:10532634 731729 Casp1 caspase 1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:11376856 731729 Casp1 caspase 1 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9015751 731729 Casp1 caspase 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:21565393 731729 Casp1 caspase 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:7859282 731729 Casp1 caspase 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:7535475 731729 Casp1 caspase 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10491411 731729 Casp1 caspase 1 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:10491411 731729 Casp1 caspase 1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:7859282 731729 Casp1 caspase 1 gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:23219391 731729 Casp1 caspase 1 gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:22002608 731729 Casp1 caspase 1 gene MP:0008639 decreased circulating interleukin-1 alpha level IAGP N RGD:5509061 20141003 MGI PMID:22002608 731729 Casp1 caspase 1 gene MP:0008639 decreased circulating interleukin-1 alpha level IAGP N RGD:5509061 20141003 MGI PMID:7859282 731729 Casp1 caspase 1 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:22002608 731729 Casp1 caspase 1 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:7859282 731729 Casp1 caspase 1 gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:14693703 731729 Casp1 caspase 1 gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:22002608 731729 Casp1 caspase 1 gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:7535475 731729 Casp1 caspase 1 gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:7859282 731729 Casp1 caspase 1 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:14663141 731729 Casp1 caspase 1 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:14693703 731729 Casp1 caspase 1 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:18493980 731729 Casp1 caspase 1 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20457908 731729 Casp1 caspase 1 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22002608 731729 Casp1 caspase 1 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:7535475 731729 Casp1 caspase 1 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:7859282 731729 Casp1 caspase 1 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:9809553 731729 Casp1 caspase 1 gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:10491411 731729 Casp1 caspase 1 gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:14693703 731729 Casp1 caspase 1 gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:22002608 731729 Casp1 caspase 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:7535475 731729 Casp1 caspase 1 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:16407889 731729 Casp1 caspase 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:22002608 731729 Casp1 caspase 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:7859282 731729 Casp1 caspase 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:9015751 731729 Casp1 caspase 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:9317135 731729 Casp1 caspase 1 gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20150702 MGI PMID:16717117 731729 Casp1 caspase 1 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:7535475 731729 Casp1 caspase 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16717117 731729 Casp1 caspase 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210121 MGI PMID:32668247 731729 Casp1 caspase 1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10639148 731729 Casp1 caspase 1 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22002608 731729 Casp1 caspase 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18493980 731729 Casp1 caspase 1 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10899911 731729 Casp1 caspase 1 gene MP:0010377 abnormal gut flora balance IAGP N RGD:5509061 20141003 MGI PMID:21565393 731729 Casp1 caspase 1 gene MP:0011081 decreased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22002608 731736 Abcb6 ATP-binding cassette, sub-family B member 6 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20181227 MGI 731736 Abcb6 ATP-binding cassette, sub-family B member 6 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22294697 731736 Abcb6 ATP-binding cassette, sub-family B member 6 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:22294697 731736 Abcb6 ATP-binding cassette, sub-family B member 6 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22294697 731736 Abcb6 ATP-binding cassette, sub-family B member 6 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22761424 731736 Abcb6 ATP-binding cassette, sub-family B member 6 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22294697 731736 Abcb6 ATP-binding cassette, sub-family B member 6 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22294697 731736 Abcb6 ATP-binding cassette, sub-family B member 6 gene MP:0031276 abnormal stress erythropoiesis IAGP N RGD:5509061 20210805 MGI PMID:22294697 731738 Synpr synaptoporin gene MP:0002064 seizures IEA N RGD:5509061 20150219 MGI 731740 Tep1 telomerase associated protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11027287 731740 Tep1 telomerase associated protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15169895 731740 Tep1 telomerase associated protein 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20210930 MGI PMID:33905568 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20220616 MGI PMID:23873233 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000073 absent craniofacial bones IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000160 kyphosis IAGP N RGD:5509061 20220616 MGI PMID:23873233 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000161 scoliosis IAGP N RGD:5509061 20220616 MGI PMID:23873233 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000162 lordosis IAGP N RGD:5509061 20220616 MGI PMID:23873233 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170817 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20210311 MGI PMID:32584792 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:16516835 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16516835 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19805360 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000447 flattened snout IAGP N RGD:5509061 20171019 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:19805360 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141030 MGI PMID:24493648 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19805360 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:19805360 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:19805360 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20200123 MGI PMID:21576358 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:19805360 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141030 MGI PMID:24493648 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001109 absent Schwann cell precursors IAGP N RGD:5509061 20141003 MGI PMID:19805360 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001147 small testis IAGP N RGD:5509061 20220616 MGI PMID:26265072 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20220616 MGI PMID:26265072 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20220616 MGI PMID:26265072 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220616 MGI PMID:26265072 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220616 MGI PMID:26265072 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001221 epidermal atrophy IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200123 MGI PMID:21576358 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20141003 MGI PMID:18077586 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20220616 MGI PMID:23873233 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20171221 MGI PMID:28346493 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20171221 MGI PMID:28346493 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170817 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001684 abnormal axial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:16516835 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:16516835 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001744 hypersecretion of corticosterone IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001925 male infertility IAGP N RGD:5509061 20220616 MGI PMID:26265072 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8702915 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20170817 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002083 premature death IAGP N RGD:5509061 20170817 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8702915 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002251 abnormal nasopharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20841350 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20841350 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170817 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20210311 MGI PMID:32584792 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19805360 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20841350 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20210311 MGI PMID:32584792 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20210311 MGI PMID:32584792 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003441 increased glycerol level IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:19805360 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20200123 MGI PMID:21576358 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003808 increased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003820 increased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20160818 MGI PMID:23929766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003958 heart valve hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:16516835 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200123 MGI PMID:21576358 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200123 MGI PMID:21576358 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:16516835 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004049 increased acute promyelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004075 decreased Schwann cell precursor number IAGP N RGD:5509061 20141003 MGI PMID:19805360 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20220616 MGI PMID:23873233 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20170817 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20220616 MGI PMID:23873233 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220616 MGI PMID:26265072 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220616 MGI PMID:26265072 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:16516835 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:16516835 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16516835 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220616 MGI PMID:26265072 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20841350 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20170817 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20170817 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20841350 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20170817 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20220616 MGI PMID:26265072 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20220616 MGI PMID:26265072 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0006394 abnormal vertebral epiphyseal plate morphology IAGP N RGD:5509061 20220616 MGI PMID:23873233 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20200123 MGI PMID:21576358 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008384 absent nasal capsule IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20210311 MGI PMID:32584792 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20200123 MGI PMID:21576358 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:21576358 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20200123 MGI PMID:21576358 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:21576358 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200123 MGI PMID:21576358 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20200123 MGI PMID:21576358 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20170817 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:19805360 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:21575863 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0009320 increased lymphoblastic lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:17015617 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:17015617 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:19805360 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20171221 MGI PMID:28346493 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0009877 exostosis IAGP N RGD:5509061 20160818 MGI PMID:23929766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20171221 MGI PMID:28346493 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010031 abnormal cranium size IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010031 abnormal cranium size IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141030 MGI PMID:24493648 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:15520383 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010464 abnormal aortic arch and aortic arch branch attachment IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010570 prolonged ST segment IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010589 common truncal valve IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010618 enlarged mitral valve IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20240125 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10411909 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8702915 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16516835 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21930766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9171349 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011103 embryonic lethality at implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16516835 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19805360 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220616 MGI PMID:26265072 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011904 abnormal Schwann cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19805360 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011904 abnormal Schwann cell physiology IAGP N RGD:5509061 20141030 MGI PMID:24493648 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20170817 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0012117 decreased trophectoderm cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16516835 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200123 MGI PMID:21576358 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200123 MGI PMID:21576358 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0012514 pectus excavatum IAGP N RGD:5509061 20210805 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0012749 decreased cardiac neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0012756 impaired cranial neural crest cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0013002 decreased enteric neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:19805360 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0013243 abnormal carbohydrate metabolism IAGP N RGD:5509061 20150625 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0013331 abnormal lacrimal gland development IAGP N RGD:5509061 20141204 MGI PMID:18077586 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20150409 MGI PMID:19179468 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220616 MGI PMID:26265072 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231221 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0020346 abnormal myocardial fiber calcium currents IAGP N RGD:5509061 20170817 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0020355 abnormal Sertoli cell barrier morphology IAGP N RGD:5509061 20220616 MGI PMID:26265072 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0020356 abnormal Sertoli cell barrier function IAGP N RGD:5509061 20220616 MGI PMID:26265072 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0030020 decreased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170817 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0030034 depressed nasal bridge IAGP N RGD:5509061 20170914 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0030166 increased inner canthal distance IAGP N RGD:5509061 20171005 MGI PMID:19251646 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0030189 broad snout IAGP N RGD:5509061 20171019 MGI PMID:15273746 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0030190 small snout IAGP N RGD:5509061 20171019 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0031277 pectus carinatum IAGP N RGD:5509061 20210805 MGI PMID:21339643 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0031414 decreased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:25288766 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0031418 increased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0031449 abnormal nasal cartilage morphology IAGP N RGD:5509061 20221110 MGI PMID:19541608 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0031580 enlarged semilunar valve IAGP N RGD:5509061 20240125 MGI PMID:10700187 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:19001090 731747 Ptpn11 protein tyrosine phosphatase, non-receptor type 11 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:19001090 731749 Batf3 basic leucine zipper transcription factor, ATF-like 3 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:19008445 731749 Batf3 basic leucine zipper transcription factor, ATF-like 3 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19008445 731749 Batf3 basic leucine zipper transcription factor, ATF-like 3 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23297132 731749 Batf3 basic leucine zipper transcription factor, ATF-like 3 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:19008445 731749 Batf3 basic leucine zipper transcription factor, ATF-like 3 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19008445 731749 Batf3 basic leucine zipper transcription factor, ATF-like 3 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22209163 731749 Batf3 basic leucine zipper transcription factor, ATF-like 3 gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:19008445 731749 Batf3 basic leucine zipper transcription factor, ATF-like 3 gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19008445 731749 Batf3 basic leucine zipper transcription factor, ATF-like 3 gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19008445 731749 Batf3 basic leucine zipper transcription factor, ATF-like 3 gene MP:0008122 decreased myeloid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:19008445 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20180412 MGI PMID:28706256 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0000745 tremors IEA N RGD:5509061 20240523 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0001406 abnormal gait IEA N RGD:5509061 20240523 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20181227 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20230601 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20240523 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20180412 MGI PMID:28706256 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20180412 MGI PMID:28706256 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20240523 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20180412 MGI PMID:28706256 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20180412 MGI PMID:28706256 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20180412 MGI PMID:28706256 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0005544 cornea deposits IEA N RGD:5509061 20181227 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20181227 MGI 731752 Slc5a5 solute carrier family 5 (sodium iodide symporter), member 5 gene MP:0011471 decreased urine creatinine level IEA N RGD:5509061 20211021 MGI 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0000274 enlarged heart IEA N RGD:5509061 20201022 MGI 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:11560960 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:16446309 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:16446309 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:16446309 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:16446309 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:16446309 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:20670678 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11560960 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:11560960 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11560960 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001435 absent suckling reflex IAGP N RGD:5509061 20141003 MGI PMID:11560960 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001437 no swallowing reflex IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:11560960 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20230601 MGI 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11560960 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0002274 abnormal type I pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0002296 aspiration IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0002989 small kidney IEA N RGD:5509061 20201022 MGI 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210128 MGI 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0003947 abnormal cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16446309 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20210429 MGI PMID:33410752 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16446309 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:17408495 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20210429 MGI PMID:33410752 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20210429 MGI PMID:33410752 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17408495 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11560960 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20670678 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:11560960 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20210429 MGI PMID:33410752 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11560960 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:17408495 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:11560960 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:11560960 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11560960 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17408495 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20210429 MGI PMID:33410752 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0010161 decreased brain cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11560960 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0010161 decreased brain cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17408495 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17408495 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11230174 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11560960 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17408495 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20210429 MGI PMID:33410752 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16446309 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0012224 abnormal sterol level IAGP N RGD:5509061 20210429 MGI PMID:33410752 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0012225 decreased sterol level IAGP N RGD:5509061 20240704 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:16446309 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0020863 abnormal suckling reflex IAGP N RGD:5509061 20220922 MGI PMID:17408495 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0031631 decreased lung cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:15005800 731756 Dhcr7 7-dehydrocholesterol reductase gene MP:0031631 decreased lung cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:17408495 731759 Capn5 calpain 5 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 731759 Capn5 calpain 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14749380 731759 Capn5 calpain 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14749380 731759 Capn5 calpain 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14749380 731759 Capn5 calpain 5 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20111116 MGI 731762 Serpina3n serine (or cysteine) peptidase inhibitor, clade A, member 3N gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20191226 MGI PMID:25915831 731762 Serpina3n serine (or cysteine) peptidase inhibitor, clade A, member 3N gene MP:0003177 allodynia IAGP N RGD:5509061 20191226 MGI PMID:25915831 731762 Serpina3n serine (or cysteine) peptidase inhibitor, clade A, member 3N gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20191226 MGI PMID:25915831 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11896201 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0000215 absent erythrocytes IAGP N RGD:5509061 20141003 MGI PMID:8696349 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:11896201 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:8696349 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:11896201 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:11896201 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:8696349 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8696349 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:8696349 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:23469164 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11896201 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12124343 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12124343 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11896201 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23469164 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8696349 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8696349 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12124343 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12124343 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11896201 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:8696349 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:11896201 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:12124343 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:8696349 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:8696349 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:8696349 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:12124343 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8696349 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20141003 MGI PMID:11896201 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0008737 abnormal spleen physiology IAGP N RGD:5509061 20141003 MGI PMID:12124343 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:11896201 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:12124343 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:8696349 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12124343 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12124343 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23469164 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11896201 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8696349 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:11896201 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:12124343 731764 Lig1 ligase I, DNA, ATP-dependent gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12124343 731766 Gucy2f guanylate cyclase 2f gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17255100 731766 Gucy2f guanylate cyclase 2f gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17255100 731766 Gucy2f guanylate cyclase 2f gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17255100 731766 Gucy2f guanylate cyclase 2f gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:17255100 731766 Gucy2f guanylate cyclase 2f gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:17255100 731766 Gucy2f guanylate cyclase 2f gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:17255100 731766 Gucy2f guanylate cyclase 2f gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:17255100 731766 Gucy2f guanylate cyclase 2f gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:17255100 731767 Gorasp2 golgi reassembly stacking protein 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170720 MGI PMID:28617811 731767 Gorasp2 golgi reassembly stacking protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20170720 MGI PMID:28617811 731767 Gorasp2 golgi reassembly stacking protein 2 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20170720 MGI PMID:28617811 731767 Gorasp2 golgi reassembly stacking protein 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20170720 MGI PMID:28617811 731767 Gorasp2 golgi reassembly stacking protein 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20170720 MGI PMID:28617811 731767 Gorasp2 golgi reassembly stacking protein 2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20170720 MGI PMID:28617811 731767 Gorasp2 golgi reassembly stacking protein 2 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20170720 MGI PMID:28617811 731767 Gorasp2 golgi reassembly stacking protein 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20170720 MGI PMID:28617811 731767 Gorasp2 golgi reassembly stacking protein 2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20170720 MGI PMID:28617811 731767 Gorasp2 golgi reassembly stacking protein 2 gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20170720 MGI PMID:28617811 731773 Hspb2 heat shock protein 2 gene MP:0002804 abnormal motor learning IEA N RGD:5509061 20160421 MGI 731773 Hspb2 heat shock protein 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 731773 Hspb2 heat shock protein 2 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:22870288 731773 Hspb2 heat shock protein 2 gene MP:0009198 abnormal male genitalia morphology IEA N RGD:5509061 20240523 MGI 731773 Hspb2 heat shock protein 2 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:22870288 731776 Haao 3-hydroxyanthranilate 3,4-dioxygenase gene MP:0000111 cleft palate IAGP N RGD:5509061 20190502 MGI PMID:28792876 731776 Haao 3-hydroxyanthranilate 3,4-dioxygenase gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20190502 MGI PMID:28792876 731776 Haao 3-hydroxyanthranilate 3,4-dioxygenase gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20190502 MGI PMID:28792876 731776 Haao 3-hydroxyanthranilate 3,4-dioxygenase gene MP:0000564 syndactyly IAGP N RGD:5509061 20190502 MGI PMID:28792876 731776 Haao 3-hydroxyanthranilate 3,4-dioxygenase gene MP:0000576 clubfoot IAGP N RGD:5509061 20190502 MGI PMID:28792876 731776 Haao 3-hydroxyanthranilate 3,4-dioxygenase gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20170817 MGI PMID:27754481 731776 Haao 3-hydroxyanthranilate 3,4-dioxygenase gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20190502 MGI PMID:28792876 731776 Haao 3-hydroxyanthranilate 3,4-dioxygenase gene MP:0002989 small kidney IAGP N RGD:5509061 20190502 MGI PMID:28792876 731776 Haao 3-hydroxyanthranilate 3,4-dioxygenase gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20170817 MGI PMID:27754481 731776 Haao 3-hydroxyanthranilate 3,4-dioxygenase gene MP:0003718 maternal effect IAGP N RGD:5509061 20190502 MGI PMID:28792876 731776 Haao 3-hydroxyanthranilate 3,4-dioxygenase gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 731776 Haao 3-hydroxyanthranilate 3,4-dioxygenase gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230601 MGI 731776 Haao 3-hydroxyanthranilate 3,4-dioxygenase gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20170817 MGI PMID:27754481 731776 Haao 3-hydroxyanthranilate 3,4-dioxygenase gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20190418 MGI PMID:28792876 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0000031 abnormal cochlea morphology IEA N RGD:5509061 20111116 MGI 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:22219655 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:22219655 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001411 spinning IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001525 impaired balance IEA N RGD:5509061 20111116 MGI 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:22219655 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0002729 abnormal inner ear canal morphology IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0002880 opisthotonus IAGP N RGD:5509061 20141003 MGI PMID:22219655 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0003145 detached otolithic membrane IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0003145 detached otolithic membrane IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004070 abnormal P wave IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004138 abnormal mucous neck cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004301 absent organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004301 absent organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004308 abnormal basilar membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004325 absent vestibular hair cells IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004334 utricular macular degeneration IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004364 thin stria vascularis IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004409 abnormal crista ampullaris neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004427 abnormal vestibular labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004518 absent vestibular hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004731 increased circulating gastrin level IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0005211 increased stomach mucosa thickness IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:22219655 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:22219655 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0006330 syndromic hearing impairment IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0006330 syndromic hearing impairment IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0008001 hypochlorhydria IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0008308 small scala media IAGP N RGD:5509061 20141003 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0008308 small scala media IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0010323 retropulsion IEA N RGD:5509061 20111116 MGI 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0010505 abnormal T wave IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0010505 abnormal T wave IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:11226272 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0010634 increased QRS amplitude IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0010799 stomach mucosa hyperplasia IAGP N RGD:5509061 20150312 MGI PMID:11120752 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15498462 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15891643 731777 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1 gene MP:0013566 dilated gastric gland IAGP N RGD:5509061 20150312 MGI PMID:11120752 731780 Tm4sf4 transmembrane 4 superfamily member 4 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20231207 MGI 731780 Tm4sf4 transmembrane 4 superfamily member 4 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 731780 Tm4sf4 transmembrane 4 superfamily member 4 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20230601 MGI 731780 Tm4sf4 transmembrane 4 superfamily member 4 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 731786 Ninj2 ninjurin 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 731786 Ninj2 ninjurin 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 731786 Ninj2 ninjurin 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20150430 MGI 731786 Ninj2 ninjurin 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 731786 Ninj2 ninjurin 2 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0020520 whitened brown adipose tissue morphology IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0031269 increased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20240627 MGI PMID:36504350 731786 Ninj2 ninjurin 2 gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240627 MGI PMID:36504350 731789 P4ha1 procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha 1 polypeptide gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17135260 731789 P4ha1 procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha 1 polypeptide gene MP:0003044 impaired basement membrane formation IAGP N RGD:5509061 20141003 MGI PMID:17135260 731789 P4ha1 procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha 1 polypeptide gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:17135260 731789 P4ha1 procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha 1 polypeptide gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17135260 731789 P4ha1 procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha 1 polypeptide gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17135260 731789 P4ha1 procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha 1 polypeptide gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20230615 MGI PMID:17135260 731789 P4ha1 procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha 1 polypeptide gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17135260 731789 P4ha1 procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha 1 polypeptide gene MP:0011261 abnormal limb mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:17135260 731791 Kcnk1 potassium channel, subfamily K, member 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:16025300 731791 Kcnk1 potassium channel, subfamily K, member 1 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:16025300 731791 Kcnk1 potassium channel, subfamily K, member 1 gene MP:0010110 abnormal renal phosphate reabsorption IAGP N RGD:5509061 20141003 MGI PMID:16025300 731791 Kcnk1 potassium channel, subfamily K, member 1 gene MP:0011432 decreased urine flow rate IAGP N RGD:5509061 20141003 MGI PMID:16025300 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20457873 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:22560297 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0002346 abnormal lymph node secondary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20457873 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17713536 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20457873 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0006423 dilated rete testis IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0008117 abnormal Langerhans cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20457873 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17713536 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20457873 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0011263 abnormal spleen mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:22560297 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:10880462 731792 Cdkn2b cyclin dependent kinase inhibitor 2B gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0001512 trunk curl IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0008570 lipidosis IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0008806 increased circulating amylase level IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:19004801 731797 Phyh phytanoyl-CoA hydroxylase gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:19004801 731800 Kif1c kinesin family member 1C gene MP:0001875 testis inflammation IAGP N RGD:5509061 20141003 MGI PMID:7777570 731800 Kif1c kinesin family member 1C gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:7777570 731800 Kif1c kinesin family member 1C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11784862 731800 Kif1c kinesin family member 1C gene MP:0002409 decreased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:14578173 731800 Kif1c kinesin family member 1C gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9720874 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:16371590 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:9192653 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:16371590 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:9192653 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9192653 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9192653 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:9192653 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20220317 MGI PMID:22357636 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220317 MGI PMID:22357636 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20141003 MGI PMID:9192653 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0013286 abnormal sperm capacitation IAGP N RGD:5509061 20191226 MGI PMID:16371590 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0013287 abnormal acrosome reaction IAGP N RGD:5509061 20191226 MGI PMID:16371590 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:16371590 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220317 MGI PMID:22357636 731802 Pcsk4 proprotein convertase subtilisin/kexin type 4 gene MP:0031355 abnormal proacrosomal vesicle fusion IAGP N RGD:5509061 20220317 MGI PMID:22357636 731804 Pygl liver glycogen phosphorylase gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20221124 MGI PMID:36077341 731804 Pygl liver glycogen phosphorylase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20221124 MGI PMID:36077341 731804 Pygl liver glycogen phosphorylase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20221124 MGI PMID:36077341 731804 Pygl liver glycogen phosphorylase gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20221124 MGI PMID:36077341 731804 Pygl liver glycogen phosphorylase gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20200310 MGI PMID:31701076 731804 Pygl liver glycogen phosphorylase gene MP:0020103 decreased hepatic glucose production IAGP N RGD:5509061 20200310 MGI PMID:31701076 731805 Col5a3 collagen, type V, alpha 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0009109 decreased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0014117 increased pancreatic beta cell apoptosis IAGP N RGD:5509061 20160324 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0014121 increased pancreatic islet cell apoptosis IAGP N RGD:5509061 20160324 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:21293061 731805 Col5a3 collagen, type V, alpha 3 gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:21293061 731807 Tnmd tenomodulin gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:15632070 731809 Avil advillin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20439739 731809 Avil advillin gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:20439739 731809 Avil advillin gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20181025 MGI PMID:30126982 731809 Avil advillin gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20439739 731809 Avil advillin gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22634729 731809 Avil advillin gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:20439739 731809 Avil advillin gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20200213 MGI PMID:30917309 731809 Avil advillin gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20200213 MGI PMID:30917309 731809 Avil advillin gene MP:0001097 abnormal superior glossopharyngeal ganglion morphology IAGP N RGD:5509061 20200213 MGI PMID:30917309 731809 Avil advillin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20439739 731809 Avil advillin gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:20439739 731809 Avil advillin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20439739 731809 Avil advillin gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:22634729 731809 Avil advillin gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:20439739 731809 Avil advillin gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:20439739 731809 Avil advillin gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20181025 MGI PMID:30126982 731809 Avil advillin gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20220922 MGI PMID:35775484 731809 Avil advillin gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:20439739 731809 Avil advillin gene MP:0003177 allodynia IAGP N RGD:5509061 20181025 MGI PMID:30126982 731809 Avil advillin gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20439739 731809 Avil advillin gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200213 MGI PMID:30917309 731809 Avil advillin gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20181025 MGI PMID:30126982 731809 Avil advillin gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20181025 MGI PMID:30126982 731809 Avil advillin gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20439739 731809 Avil advillin gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20181025 MGI PMID:30126982 731809 Avil advillin gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:20439739 731809 Avil advillin gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20220922 MGI PMID:35775484 731809 Avil advillin gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:20439739 731809 Avil advillin gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20181025 MGI PMID:30126982 731809 Avil advillin gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18160648 731809 Avil advillin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20439739 731809 Avil advillin gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18160648 731809 Avil advillin gene MP:0014491 abnormal mammary gland sensory innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:23224557 731809 Avil advillin gene MP:0030012 impaired central nervous system regeneration IAGP N RGD:5509061 20170713 MGI PMID:18160648 731813 Hcn3 hyperpolarization-activated, cyclic nucleotide-gated K+ 3 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:21903939 731813 Hcn3 hyperpolarization-activated, cyclic nucleotide-gated K+ 3 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:21903939 731813 Hcn3 hyperpolarization-activated, cyclic nucleotide-gated K+ 3 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:21903939 731813 Hcn3 hyperpolarization-activated, cyclic nucleotide-gated K+ 3 gene MP:0010505 abnormal T wave IAGP N RGD:5509061 20141003 MGI PMID:21903939 731817 Msi1 musashi RNA-binding protein 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12407178 731817 Msi1 musashi RNA-binding protein 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:12407178 731817 Msi1 musashi RNA-binding protein 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12407178 731817 Msi1 musashi RNA-binding protein 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:12407178 731817 Msi1 musashi RNA-binding protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12407178 731817 Msi1 musashi RNA-binding protein 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:12407178 731817 Msi1 musashi RNA-binding protein 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:12407178 731817 Msi1 musashi RNA-binding protein 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:12407178 731817 Msi1 musashi RNA-binding protein 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23132814 731817 Msi1 musashi RNA-binding protein 1 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12407178 731817 Msi1 musashi RNA-binding protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12407178 731817 Msi1 musashi RNA-binding protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23132814 731817 Msi1 musashi RNA-binding protein 1 gene MP:0002653 abnormal ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:12407178 731817 Msi1 musashi RNA-binding protein 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20200123 MGI PMID:18662689 731817 Msi1 musashi RNA-binding protein 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200123 MGI PMID:18662689 731817 Msi1 musashi RNA-binding protein 1 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20200123 MGI PMID:18662689 731817 Msi1 musashi RNA-binding protein 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:18662689 731817 Msi1 musashi RNA-binding protein 1 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200123 MGI PMID:18662689 731817 Msi1 musashi RNA-binding protein 1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20200123 MGI PMID:18662689 731821 Cdh2 cadherin 2 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15614770 731821 Cdh2 cadherin 2 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9015265 731821 Cdh2 cadherin 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9015265 731821 Cdh2 cadherin 2 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:15662031 731821 Cdh2 cadherin 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15662031 731821 Cdh2 cadherin 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9015265 731821 Cdh2 cadherin 2 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:9015265 731821 Cdh2 cadherin 2 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 731821 Cdh2 cadherin 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 731821 Cdh2 cadherin 2 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20150101 MGI PMID:25100583 731821 Cdh2 cadherin 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:15614770 731821 Cdh2 cadherin 2 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:9015265 731821 Cdh2 cadherin 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:22036570 731821 Cdh2 cadherin 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20230302 MGI PMID:34702855 731821 Cdh2 cadherin 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20230302 MGI PMID:34702855 731821 Cdh2 cadherin 2 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20230302 MGI PMID:34702855 731821 Cdh2 cadherin 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15662031 731821 Cdh2 cadherin 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:15662031 731821 Cdh2 cadherin 2 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:10545229 731821 Cdh2 cadherin 2 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:10545229 731821 Cdh2 cadherin 2 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:9015265 731821 Cdh2 cadherin 2 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9015265 731821 Cdh2 cadherin 2 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:9015265 731821 Cdh2 cadherin 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:15614770 731821 Cdh2 cadherin 2 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20230302 MGI PMID:34702855 731821 Cdh2 cadherin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15662031 731821 Cdh2 cadherin 2 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:15662031 731821 Cdh2 cadherin 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20240530 MGI PMID:33494786 731821 Cdh2 cadherin 2 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15662031 731821 Cdh2 cadherin 2 gene MP:0002634 abnormal sensorimotor gating IAGP N RGD:5509061 20230302 MGI PMID:34702855 731821 Cdh2 cadherin 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15662031 731821 Cdh2 cadherin 2 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15662031 731821 Cdh2 cadherin 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20240530 MGI PMID:33494786 731821 Cdh2 cadherin 2 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20240530 MGI PMID:33494786 731821 Cdh2 cadherin 2 gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20230302 MGI PMID:34702855 731821 Cdh2 cadherin 2 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:15662031 731821 Cdh2 cadherin 2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:15662031 731821 Cdh2 cadherin 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9015265 731821 Cdh2 cadherin 2 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:15662031 731821 Cdh2 cadherin 2 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 731821 Cdh2 cadherin 2 gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20230302 MGI PMID:34702855 731821 Cdh2 cadherin 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9015265 731821 Cdh2 cadherin 2 gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20230302 MGI PMID:34702855 731821 Cdh2 cadherin 2 gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20230302 MGI PMID:34702855 731821 Cdh2 cadherin 2 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20230302 MGI PMID:34702855 731821 Cdh2 cadherin 2 gene MP:0004793 abnormal synaptic vesicle clustering IAGP N RGD:5509061 20230302 MGI PMID:34702855 731821 Cdh2 cadherin 2 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20150101 MGI PMID:25100583 731821 Cdh2 cadherin 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9015265 731821 Cdh2 cadherin 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15662031 731821 Cdh2 cadherin 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:22036570 731821 Cdh2 cadherin 2 gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:15662031 731821 Cdh2 cadherin 2 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 731821 Cdh2 cadherin 2 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20150101 MGI PMID:25100583 731821 Cdh2 cadherin 2 gene MP:0009455 enhanced cued conditioning behavior IAGP N RGD:5509061 20240530 MGI PMID:33494786 731821 Cdh2 cadherin 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20230302 MGI PMID:34702855 731821 Cdh2 cadherin 2 gene MP:0009685 abnormal spinal cord motor column morphology IAGP N RGD:5509061 20141003 MGI PMID:22036570 731821 Cdh2 cadherin 2 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20240530 MGI PMID:33494786 731821 Cdh2 cadherin 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22036570 731821 Cdh2 cadherin 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15614770 731821 Cdh2 cadherin 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9015265 731821 Cdh2 cadherin 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22036570 731821 Cdh2 cadherin 2 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20230302 MGI PMID:34702855 731821 Cdh2 cadherin 2 gene MP:0011723 ectopic neuron IAGP N RGD:5509061 20150101 MGI PMID:25100583 731821 Cdh2 cadherin 2 gene MP:0014369 enhanced spatial working memory IAGP N RGD:5509061 20240530 MGI PMID:33494786 731821 Cdh2 cadherin 2 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:34702855 731821 Cdh2 cadherin 2 gene MP:0020360 abnormal asymmetric synapse morphology IAGP N RGD:5509061 20240530 MGI PMID:33494786 731821 Cdh2 cadherin 2 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20240530 MGI PMID:33494786 731821 Cdh2 cadherin 2 gene MP:0020875 decreased nervous system dopamine level IAGP N RGD:5509061 20230302 MGI PMID:34702855 731821 Cdh2 cadherin 2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15662031 731824 Atp5mc2 ATP synthase membrane subunit c locus 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230720 MGI 731824 Atp5mc2 ATP synthase membrane subunit c locus 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 731824 Atp5mc2 ATP synthase membrane subunit c locus 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20230720 MGI 731824 Atp5mc2 ATP synthase membrane subunit c locus 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20230720 MGI 731824 Atp5mc2 ATP synthase membrane subunit c locus 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230720 MGI 731824 Atp5mc2 ATP synthase membrane subunit c locus 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20230720 MGI 731824 Atp5mc2 ATP synthase membrane subunit c locus 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230720 MGI 731825 Anxa2 annexin A2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:14702107 731825 Anxa2 annexin A2 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14702107 731825 Anxa2 annexin A2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14702107 731825 Anxa2 annexin A2 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:14702107 731825 Anxa2 annexin A2 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:14702107 731825 Anxa2 annexin A2 gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:14702107 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0000371 diluted coat color IEA N RGD:5509061 20111116 MGI 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12538872 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:849254 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:9585243 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0002764 short tibia IEA N RGD:5509061 20220811 MGI 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0003068 enlarged kidney IEA N RGD:5509061 20220519 MGI 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20220519 MGI 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:12538872 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0005100 abnormal choroid pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9585243 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18715234 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9585243 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:12538872 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:9585243 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:6696991 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:9585243 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 731827 Vps33a VPS33A CORVET/HOPS core subunit gene MP:0030918 small melanosome IAGP N RGD:5509061 20181227 MGI PMID:12538872 731831 Vegfd vascular endothelial growth factor D gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 731831 Vegfd vascular endothelial growth factor D gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 731831 Vegfd vascular endothelial growth factor D gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 731831 Vegfd vascular endothelial growth factor D gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 731831 Vegfd vascular endothelial growth factor D gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:19718705 731831 Vegfd vascular endothelial growth factor D gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18519586 731831 Vegfd vascular endothelial growth factor D gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18519586 731831 Vegfd vascular endothelial growth factor D gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15743836 731831 Vegfd vascular endothelial growth factor D gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18519586 731831 Vegfd vascular endothelial growth factor D gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:19022221 731834 Cdc20 cell division cycle 20 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:19528295 731834 Cdc20 cell division cycle 20 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19528295 731834 Cdc20 cell division cycle 20 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21156286 731834 Cdc20 cell division cycle 20 gene MP:0000423 delayed hair regrowth IAGP N RGD:5509061 20141003 MGI PMID:21156286 731834 Cdc20 cell division cycle 20 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21156286 731834 Cdc20 cell division cycle 20 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20941357 731834 Cdc20 cell division cycle 20 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:21156286 731834 Cdc20 cell division cycle 20 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21156286 731834 Cdc20 cell division cycle 20 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19528295 731834 Cdc20 cell division cycle 20 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:20941357 731834 Cdc20 cell division cycle 20 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20941357 731834 Cdc20 cell division cycle 20 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19528295 731834 Cdc20 cell division cycle 20 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21156286 731834 Cdc20 cell division cycle 20 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 731834 Cdc20 cell division cycle 20 gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:21156286 731834 Cdc20 cell division cycle 20 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21156286 731834 Cdc20 cell division cycle 20 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17325031 731834 Cdc20 cell division cycle 20 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:20941357 731834 Cdc20 cell division cycle 20 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:19528295 731834 Cdc20 cell division cycle 20 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:20941357 731834 Cdc20 cell division cycle 20 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:19528295 731834 Cdc20 cell division cycle 20 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:21156286 731834 Cdc20 cell division cycle 20 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:20941357 731834 Cdc20 cell division cycle 20 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20170105 MGI 731834 Cdc20 cell division cycle 20 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20211021 MGI 731834 Cdc20 cell division cycle 20 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160421 MGI 731834 Cdc20 cell division cycle 20 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20941357 731834 Cdc20 cell division cycle 20 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 731834 Cdc20 cell division cycle 20 gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19528295 731834 Cdc20 cell division cycle 20 gene MP:0010537 tumor regression IAGP N RGD:5509061 20141003 MGI PMID:21156286 731834 Cdc20 cell division cycle 20 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17325031 731834 Cdc20 cell division cycle 20 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21156286 731834 Cdc20 cell division cycle 20 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17325031 731834 Cdc20 cell division cycle 20 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19528295 731834 Cdc20 cell division cycle 20 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731834 Cdc20 cell division cycle 20 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17325031 731834 Cdc20 cell division cycle 20 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19528295 731834 Cdc20 cell division cycle 20 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 731834 Cdc20 cell division cycle 20 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 731834 Cdc20 cell division cycle 20 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 731834 Cdc20 cell division cycle 20 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:19528295 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20150319 MGI PMID:9139708 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:19760322 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:8755578 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20150319 MGI PMID:9139708 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150319 MGI PMID:9139708 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220519 MGI PMID:8755578 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19760322 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150319 MGI PMID:9139708 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:8755578 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:11095909 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:11463821 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:8755578 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001304 cataract IAGP N RGD:5509061 20150319 MGI PMID:9139708 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20150319 MGI PMID:9139708 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20150319 MGI PMID:9139708 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11463821 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:11463821 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001924 infertility IEA N RGD:5509061 20111116 MGI 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20150319 MGI PMID:9139708 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20150319 MGI PMID:9139708 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0001937 abnormal sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:11463821 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11463821 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8755578 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8755578 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11463821 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8755578 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20150319 MGI PMID:9139708 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:8755578 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:19760322 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:12810527 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:19760322 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:19760322 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0003415 priapism IAGP N RGD:5509061 20150319 MGI PMID:9139708 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:12810527 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:19760322 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20141003 MGI PMID:8755578 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:12810527 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:19760322 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0004932 epididymis hypoplasia IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0004984 increased osteoclast cell number IEA N RGD:5509061 20111116 MGI 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0005148 seminal vesicle hypoplasia IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0005158 ovary hypoplasia IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0005471 decreased thyroxine level IEA N RGD:5509061 20111116 MGI 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:19760322 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0008477 decreased spleen red pulp amount IEA N RGD:5509061 20111116 MGI 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0008912 nervous IAGP N RGD:5509061 20150319 MGI PMID:9139708 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:11095909 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0011130 absent tertiary ovarian follicles IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0012604 decreased glutathione level IAGP N RGD:5509061 20150409 MGI PMID:9139708 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0013730 glutathionuria IAGP N RGD:5509061 20150416 MGI PMID:9139708 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0030623 decreased cysteine level IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0030626 decreased circulating cysteine level IAGP N RGD:5509061 20180920 MGI PMID:8755578 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0030653 increased circulating glutathione level IAGP N RGD:5509061 20180913 MGI PMID:9139708 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0030983 failure of copulatory plug deposition IAGP N RGD:5509061 20220519 MGI PMID:11089562 731835 Ggt1 gamma-glutamyltransferase 1 gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220630 MGI PMID:11089562 731836 Slc15a3 solute carrier family 15, member 3 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20201022 MGI 731836 Slc15a3 solute carrier family 15, member 3 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 731836 Slc15a3 solute carrier family 15, member 3 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20160421 MGI 731836 Slc15a3 solute carrier family 15, member 3 gene MP:0006173 abnormal myeloid dendritic cell morphology IAGP N RGD:5509061 20180201 MGI PMID:24695226 731836 Slc15a3 solute carrier family 15, member 3 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 731838 Cga glycoprotein hormones, alpha subunit gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0005119 decreased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0008329 decreased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0008332 decreased lactotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0008333 absent lactotrophs IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0008337 increased thyrotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:7544315 731838 Cga glycoprotein hormones, alpha subunit gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:7544315 731839 Adcy4 adenylate cyclase 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151112 MGI PMID:24760529 731846 Ces1e carboxylesterase 1E gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:3101673 731846 Ces1e carboxylesterase 1E gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:7236294 731846 Ces1e carboxylesterase 1E gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:3101673 731847 Per3 period circadian clock 3 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:21810984 731847 Per3 period circadian clock 3 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:15031135 731847 Per3 period circadian clock 3 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20160324 MGI PMID:26903630 731847 Per3 period circadian clock 3 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:15031135 731847 Per3 period circadian clock 3 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21810984 731847 Per3 period circadian clock 3 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:10938103 731847 Per3 period circadian clock 3 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:11395012 731854 Rbck1 RanBP-type and C3HC4-type zinc finger containing 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 731854 Rbck1 RanBP-type and C3HC4-type zinc finger containing 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19136968 731855 Hhex hematopoietically expressed homeobox gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:11027604 731855 Hhex hematopoietically expressed homeobox gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17580084 731855 Hhex hematopoietically expressed homeobox gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17580084 731855 Hhex hematopoietically expressed homeobox gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11027604 731855 Hhex hematopoietically expressed homeobox gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:21445260 731855 Hhex hematopoietically expressed homeobox gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11027604 731855 Hhex hematopoietically expressed homeobox gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18940732 731855 Hhex hematopoietically expressed homeobox gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:21445260 731855 Hhex hematopoietically expressed homeobox gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:17580084 731855 Hhex hematopoietically expressed homeobox gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:21445260 731855 Hhex hematopoietically expressed homeobox gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0003250 absent gallbladder IAGP N RGD:5509061 20141003 MGI PMID:17580084 731855 Hhex hematopoietically expressed homeobox gene MP:0003266 biliary cyst IAGP N RGD:5509061 20141003 MGI PMID:17580084 731855 Hhex hematopoietically expressed homeobox gene MP:0003327 liver cyst IAGP N RGD:5509061 20141003 MGI PMID:17580084 731855 Hhex hematopoietically expressed homeobox gene MP:0003421 abnormal thyroid gland development IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0003421 abnormal thyroid gland development IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0003421 abnormal thyroid gland development IAGP N RGD:5509061 20141003 MGI PMID:15581879 731855 Hhex hematopoietically expressed homeobox gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0003808 increased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21445260 731855 Hhex hematopoietically expressed homeobox gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0006292 abnormal nasal placode morphology IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0006293 absent nasal placodes IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0008112 abnormal monocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:11027604 731855 Hhex hematopoietically expressed homeobox gene MP:0008533 abnormal anterior visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:21445260 731855 Hhex hematopoietically expressed homeobox gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0008926 abnormal anterior definitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0009497 abnormal intrahepatic bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:17580084 731855 Hhex hematopoietically expressed homeobox gene MP:0009498 abnormal extrahepatic bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:17580084 731855 Hhex hematopoietically expressed homeobox gene MP:0009501 abnormal hepatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:17580084 731855 Hhex hematopoietically expressed homeobox gene MP:0010335 fused first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0010449 heart right ventricle outflow tract stenosis IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0010588 conotruncal ridge hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:21445260 731855 Hhex hematopoietically expressed homeobox gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17580084 731855 Hhex hematopoietically expressed homeobox gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18940732 731855 Hhex hematopoietically expressed homeobox gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11027604 731855 Hhex hematopoietically expressed homeobox gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21445260 731855 Hhex hematopoietically expressed homeobox gene MP:0011759 absent Rathke's pouch IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0011877 absent liver IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0011877 absent liver IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:15459110 731855 Hhex hematopoietically expressed homeobox gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0012234 abnormal hepatic diverticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0012235 abnormal liver bud morphology IAGP N RGD:5509061 20141003 MGI PMID:11027604 731855 Hhex hematopoietically expressed homeobox gene MP:0012245 abnormal hepatoblast migration IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:10804184 731855 Hhex hematopoietically expressed homeobox gene MP:0013906 absent embryonic telencephalon IAGP N RGD:5509061 20150924 MGI PMID:10804184 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20111116 MGI 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0000341 abnormal bile color IAGP N RGD:5509061 20170413 MGI PMID:7544347 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0000599 enlarged liver IAGP N RGD:5509061 20170413 MGI PMID:7544347 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170413 MGI PMID:14580373 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20170413 MGI PMID:7544347 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0001511 disheveled coat IAGP N RGD:5509061 20170413 MGI PMID:7544347 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20170413 MGI PMID:10487856 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0001657 abnormal induced morbidity/mortality IAGP N RGD:5509061 20170413 MGI PMID:10487856 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20170413 MGI PMID:14580373 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0001860 liver inflammation IAGP N RGD:5509061 20170413 MGI PMID:10487856 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20170413 MGI PMID:7544347 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0001935 decreased litter size IAGP N RGD:5509061 20170413 MGI PMID:14580373 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170413 MGI PMID:7544347 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20170413 MGI PMID:7544347 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0002830 gallstones IAGP N RGD:5509061 20170413 MGI PMID:7544347 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20170413 MGI PMID:12069948 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20170413 MGI PMID:14580373 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20170413 MGI PMID:12069948 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20170413 MGI PMID:14580373 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0003849 greasy coat IAGP N RGD:5509061 20170413 MGI PMID:7544347 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20170413 MGI PMID:14580373 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20170413 MGI PMID:14580373 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20170413 MGI PMID:7544347 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20170413 MGI PMID:14580373 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0005333 decreased heart rate IEA N RGD:5509061 20111116 MGI 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20170413 MGI PMID:10487856 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0008054 abnormal uterine NK cell morphology IAGP N RGD:5509061 20170413 MGI PMID:14580373 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20170413 MGI PMID:10487856 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0008806 increased circulating amylase level IAGP N RGD:5509061 20170413 MGI PMID:10487856 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20170413 MGI PMID:10487856 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20170413 MGI PMID:10487856 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20170413 MGI PMID:10487856 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20170413 MGI PMID:7544347 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20170413 MGI PMID:7544347 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170413 MGI PMID:14580373 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0011886 increased circulating lipase level IAGP N RGD:5509061 20170413 MGI PMID:10487856 731856 Pzp PZP, alpha-2-macroglobulin like gene MP:0012726 abnormal uterine spiral artery morphology IAGP N RGD:5509061 20170413 MGI PMID:14580373 731857 Xiap X-linked inhibitor of apoptosis gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18708583 731857 Xiap X-linked inhibitor of apoptosis gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:22327219 731857 Xiap X-linked inhibitor of apoptosis gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:15540113 731857 Xiap X-linked inhibitor of apoptosis gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22327219 731857 Xiap X-linked inhibitor of apoptosis gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22327219 731857 Xiap X-linked inhibitor of apoptosis gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11313486 731857 Xiap X-linked inhibitor of apoptosis gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22327219 731857 Xiap X-linked inhibitor of apoptosis gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:22327219 731857 Xiap X-linked inhibitor of apoptosis gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:15540113 731857 Xiap X-linked inhibitor of apoptosis gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18708583 731857 Xiap X-linked inhibitor of apoptosis gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22327219 731857 Xiap X-linked inhibitor of apoptosis gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:22327219 731857 Xiap X-linked inhibitor of apoptosis gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:22327219 731857 Xiap X-linked inhibitor of apoptosis gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18708583 731857 Xiap X-linked inhibitor of apoptosis gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:18708583 731857 Xiap X-linked inhibitor of apoptosis gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 731857 Xiap X-linked inhibitor of apoptosis gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 731857 Xiap X-linked inhibitor of apoptosis gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 731857 Xiap X-linked inhibitor of apoptosis gene MP:0013716 hypolactation IAGP N RGD:5509061 20150611 MGI PMID:15540113 731859 Nf2 neurofibromin 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20220428 MGI PMID:33075808 731859 Nf2 neurofibromin 2 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20643348 731859 Nf2 neurofibromin 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:18328429 731859 Nf2 neurofibromin 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:20643348 731859 Nf2 neurofibromin 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20150910 MGI PMID:26109051 731859 Nf2 neurofibromin 2 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20160811 MGI PMID:26359368 731859 Nf2 neurofibromin 2 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19487675 731859 Nf2 neurofibromin 2 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18328429 731859 Nf2 neurofibromin 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:20643348 731859 Nf2 neurofibromin 2 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:20643348 731859 Nf2 neurofibromin 2 gene MP:0001394 circling IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23455610 731859 Nf2 neurofibromin 2 gene MP:0001410 head bobbing IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0001512 trunk curl IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9171370 731859 Nf2 neurofibromin 2 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:9171370 731859 Nf2 neurofibromin 2 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9171370 731859 Nf2 neurofibromin 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:9171370 731859 Nf2 neurofibromin 2 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:17924978 731859 Nf2 neurofibromin 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:23455610 731859 Nf2 neurofibromin 2 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9553042 731859 Nf2 neurofibromin 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 731859 Nf2 neurofibromin 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 731859 Nf2 neurofibromin 2 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 731859 Nf2 neurofibromin 2 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9553042 731859 Nf2 neurofibromin 2 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0002030 increased neurofibrosarcoma incidence IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9553042 731859 Nf2 neurofibromin 2 gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 731859 Nf2 neurofibromin 2 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9553042 731859 Nf2 neurofibromin 2 gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21242963 731859 Nf2 neurofibromin 2 gene MP:0002049 increased extremity angiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18328429 731859 Nf2 neurofibromin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19487675 731859 Nf2 neurofibromin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21242963 731859 Nf2 neurofibromin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:9171370 731859 Nf2 neurofibromin 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9171370 731859 Nf2 neurofibromin 2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9171370 731859 Nf2 neurofibromin 2 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:9171370 731859 Nf2 neurofibromin 2 gene MP:0002583 absent extraembryonic ectoderm IAGP N RGD:5509061 20141003 MGI PMID:9171370 731859 Nf2 neurofibromin 2 gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:9171370 731859 Nf2 neurofibromin 2 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0003053 delayed tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20643348 731859 Nf2 neurofibromin 2 gene MP:0003252 abnormal bile duct physiology IAGP N RGD:5509061 20150910 MGI PMID:26109051 731859 Nf2 neurofibromin 2 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20141003 MGI PMID:20643348 731859 Nf2 neurofibromin 2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20643348 731859 Nf2 neurofibromin 2 gene MP:0003570 increased uterus leiomyoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 731859 Nf2 neurofibromin 2 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21242963 731859 Nf2 neurofibromin 2 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9553042 731859 Nf2 neurofibromin 2 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20220428 MGI PMID:33075808 731859 Nf2 neurofibromin 2 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0004839 bile duct hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20643348 731859 Nf2 neurofibromin 2 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20220428 MGI PMID:33075808 731859 Nf2 neurofibromin 2 gene MP:0005191 head tilt IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20220428 MGI PMID:33075808 731859 Nf2 neurofibromin 2 gene MP:0005262 coloboma IAGP N RGD:5509061 20220428 MGI PMID:33075808 731859 Nf2 neurofibromin 2 gene MP:0005307 head tossing IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:23455610 731859 Nf2 neurofibromin 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:23455610 731859 Nf2 neurofibromin 2 gene MP:0005549 retina pigment epithelium hyperplasia IAGP N RGD:5509061 20220428 MGI PMID:33075808 731859 Nf2 neurofibromin 2 gene MP:0005623 abnormal meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:17924978 731859 Nf2 neurofibromin 2 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17924978 731859 Nf2 neurofibromin 2 gene MP:0008490 enlarged dorsal root ganglion IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20220428 MGI PMID:33075808 731859 Nf2 neurofibromin 2 gene MP:0010280 increased skeletal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0010281 increased nervous system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0010281 increased nervous system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21242963 731859 Nf2 neurofibromin 2 gene MP:0010297 increased hepatobiliary system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20643348 731859 Nf2 neurofibromin 2 gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20150910 MGI PMID:26109051 731859 Nf2 neurofibromin 2 gene MP:0010309 increased mesothelioma incidence IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0010309 increased mesothelioma incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 731859 Nf2 neurofibromin 2 gene MP:0010310 increased Schwannoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0010310 increased Schwannoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0010310 increased Schwannoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18328429 731859 Nf2 neurofibromin 2 gene MP:0010310 increased Schwannoma incidence IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0010311 increased meningioma incidence IAGP N RGD:5509061 20141003 MGI PMID:17924978 731859 Nf2 neurofibromin 2 gene MP:0010311 increased meningioma incidence IAGP N RGD:5509061 20141003 MGI PMID:21242963 731859 Nf2 neurofibromin 2 gene MP:0010313 increased osteoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0010313 increased osteoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0010313 increased osteoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17924978 731859 Nf2 neurofibromin 2 gene MP:0010313 increased osteoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21242963 731859 Nf2 neurofibromin 2 gene MP:0010314 increased neurofibroma incidence IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0010314 increased neurofibroma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20160811 MGI PMID:26359368 731859 Nf2 neurofibromin 2 gene MP:0010334 pleural effusion IAGP N RGD:5509061 20141003 MGI PMID:18328429 731859 Nf2 neurofibromin 2 gene MP:0010347 osseous metaplasia IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0010347 osseous metaplasia IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0010347 osseous metaplasia IAGP N RGD:5509061 20141003 MGI PMID:17924978 731859 Nf2 neurofibromin 2 gene MP:0010353 increased odontoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0010354 increased odontosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9553042 731859 Nf2 neurofibromin 2 gene MP:0010364 increased fibroadenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0010384 increased renal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0010384 increased renal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15221010 731859 Nf2 neurofibromin 2 gene MP:0010384 increased renal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19487675 731859 Nf2 neurofibromin 2 gene MP:0010742 increased Schwann cell number IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19487675 731859 Nf2 neurofibromin 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19487675 731859 Nf2 neurofibromin 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10887156 731859 Nf2 neurofibromin 2 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9171370 731859 Nf2 neurofibromin 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19487675 731859 Nf2 neurofibromin 2 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9171370 731859 Nf2 neurofibromin 2 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20150402 MGI PMID:25113746 731859 Nf2 neurofibromin 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9553042 731859 Nf2 neurofibromin 2 gene MP:0012534 abnormal optic fissure morphology IAGP N RGD:5509061 20220428 MGI PMID:33075808 731859 Nf2 neurofibromin 2 gene MP:0013611 abnormal bile duct epithelium morphology IAGP N RGD:5509061 20150910 MGI PMID:26109051 731866 Sumo2 small ubiquitin-like modifier 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20151112 MGI PMID:24891386 731866 Sumo2 small ubiquitin-like modifier 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151112 MGI PMID:24891386 731866 Sumo2 small ubiquitin-like modifier 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20151112 MGI PMID:24891386 731866 Sumo2 small ubiquitin-like modifier 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20151112 MGI PMID:24891386 731866 Sumo2 small ubiquitin-like modifier 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151112 MGI PMID:24891386 731866 Sumo2 small ubiquitin-like modifier 2 gene MP:0003794 delayed somite formation IAGP N RGD:5509061 20151112 MGI PMID:24891386 731866 Sumo2 small ubiquitin-like modifier 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20151112 MGI PMID:24891386 731866 Sumo2 small ubiquitin-like modifier 2 gene MP:0005030 absent amnion IAGP N RGD:5509061 20151112 MGI PMID:24891386 731866 Sumo2 small ubiquitin-like modifier 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20151112 MGI PMID:24891386 731866 Sumo2 small ubiquitin-like modifier 2 gene MP:0006323 abnormal extraembryonic mesoderm development IAGP N RGD:5509061 20151112 MGI PMID:24891386 731866 Sumo2 small ubiquitin-like modifier 2 gene MP:0009656 delayed chorioallantoic fusion IAGP N RGD:5509061 20151112 MGI PMID:24891386 731866 Sumo2 small ubiquitin-like modifier 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20151112 MGI PMID:24891386 731866 Sumo2 small ubiquitin-like modifier 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20151112 MGI PMID:24891386 731866 Sumo2 small ubiquitin-like modifier 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20151112 MGI PMID:24891386 731866 Sumo2 small ubiquitin-like modifier 2 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20151112 MGI PMID:24891386 731867 Cyp2a5 cytochrome P450, family 2, subfamily a, polypeptide 5 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:19923441 731868 Npb neuropeptide B gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15983370 731868 Npb neuropeptide B gene MP:0005407 hyperalgesia IAGP N RGD:5509061 20141003 MGI PMID:15983370 731869 Plcd4 phospholipase C, delta 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 731869 Plcd4 phospholipase C, delta 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11340203 731869 Plcd4 phospholipase C, delta 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12695499 731869 Plcd4 phospholipase C, delta 4 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:11340203 731869 Plcd4 phospholipase C, delta 4 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:12695499 731869 Plcd4 phospholipase C, delta 4 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:12695499 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200423 MGI PMID:31570606 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20200423 MGI PMID:31570606 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20200423 MGI PMID:31570606 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20200423 MGI PMID:31570606 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20200423 MGI PMID:31570606 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20200423 MGI PMID:31570606 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0010039 abnormal trophoblast giant cell proliferation IAGP N RGD:5509061 20200423 MGI PMID:31570606 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20200423 MGI PMID:31570606 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0011653 decreased circulating histidine level IAGP N RGD:5509061 20200423 MGI PMID:31570606 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0012109 decreased trophoblast glycogen cell number IAGP N RGD:5509061 20200423 MGI PMID:31570606 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0030656 decreased circulating glycine level IAGP N RGD:5509061 20200423 MGI PMID:31570606 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0030695 decreased circulating serine level IAGP N RGD:5509061 20200423 MGI PMID:31570606 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0030710 decreased circulating glutamine level IAGP N RGD:5509061 20200423 MGI PMID:31570606 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0030716 decreased circulating isoleucine level IAGP N RGD:5509061 20200423 MGI PMID:31570606 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0030719 decreased circulating lysine level IAGP N RGD:5509061 20200423 MGI PMID:31570606 731870 Slc38a4 solute carrier family 38, member 4 gene MP:0030728 decreased circulating valine level IAGP N RGD:5509061 20200423 MGI PMID:31570606 731871 Syk spleen tyrosine kinase gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20230750 731871 Syk spleen tyrosine kinase gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20141003 MGI 731871 Syk spleen tyrosine kinase gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20230750 731871 Syk spleen tyrosine kinase gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:7477353 731871 Syk spleen tyrosine kinase gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20141003 MGI PMID:7477353 731871 Syk spleen tyrosine kinase gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:20230750 731871 Syk spleen tyrosine kinase gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20230750 731871 Syk spleen tyrosine kinase gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:22186994 731871 Syk spleen tyrosine kinase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 731871 Syk spleen tyrosine kinase gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20230750 731871 Syk spleen tyrosine kinase gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:22186994 731871 Syk spleen tyrosine kinase gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:22186994 731871 Syk spleen tyrosine kinase gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12563261 731871 Syk spleen tyrosine kinase gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7477352 731871 Syk spleen tyrosine kinase gene MP:0001876 decreased inflammatory response IEA N RGD:5509061 20160616 MGI 731871 Syk spleen tyrosine kinase gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20230750 731871 Syk spleen tyrosine kinase gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:22186994 731871 Syk spleen tyrosine kinase gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7477352 731871 Syk spleen tyrosine kinase gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7477353 731871 Syk spleen tyrosine kinase gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22186994 731871 Syk spleen tyrosine kinase gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20230750 731871 Syk spleen tyrosine kinase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7477353 731871 Syk spleen tyrosine kinase gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:7477353 731871 Syk spleen tyrosine kinase gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:19219027 731871 Syk spleen tyrosine kinase gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:19797524 731871 Syk spleen tyrosine kinase gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:19797524 731871 Syk spleen tyrosine kinase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0002869 increased anti-insulin autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20230750 731871 Syk spleen tyrosine kinase gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 731871 Syk spleen tyrosine kinase gene MP:0004106 lymphatic vessel hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20230750 731871 Syk spleen tyrosine kinase gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:20230750 731871 Syk spleen tyrosine kinase gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23955076 731871 Syk spleen tyrosine kinase gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22186994 731871 Syk spleen tyrosine kinase gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:15073337 731871 Syk spleen tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0005074 impaired granulocyte bactericidal activity IAGP N RGD:5509061 20141003 MGI PMID:19797524 731871 Syk spleen tyrosine kinase gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16713566 731871 Syk spleen tyrosine kinase gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:22186994 731871 Syk spleen tyrosine kinase gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:22186994 731871 Syk spleen tyrosine kinase gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22186994 731871 Syk spleen tyrosine kinase gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:7477352 731871 Syk spleen tyrosine kinase gene MP:0008053 abnormal NK cell differentiation IEA N RGD:5509061 20160616 MGI 731871 Syk spleen tyrosine kinase gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0008233 abnormal pro-B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18356083 731871 Syk spleen tyrosine kinase gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:15073337 731871 Syk spleen tyrosine kinase gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0008560 increased tumor necrosis factor secretion IEA N RGD:5509061 20141003 MGI 731871 Syk spleen tyrosine kinase gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19797524 731871 Syk spleen tyrosine kinase gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20230750 731871 Syk spleen tyrosine kinase gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 731871 Syk spleen tyrosine kinase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 731871 Syk spleen tyrosine kinase gene MP:0010130 decreased DN1 thymic pro-T cell number IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0010195 abnormal lymphatic vessel endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20230750 731871 Syk spleen tyrosine kinase gene MP:0010197 abnormal lymphatic vessel endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22186994 731871 Syk spleen tyrosine kinase gene MP:0010198 decreased lymphatic vessel endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:22186994 731871 Syk spleen tyrosine kinase gene MP:0010200 enlarged lymphatic vessel IAGP N RGD:5509061 20141003 MGI PMID:20230750 731871 Syk spleen tyrosine kinase gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:22186994 731871 Syk spleen tyrosine kinase gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7477352 731871 Syk spleen tyrosine kinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7477353 731871 Syk spleen tyrosine kinase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7477352 731871 Syk spleen tyrosine kinase gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12563261 731871 Syk spleen tyrosine kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731871 Syk spleen tyrosine kinase gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:22728826 731871 Syk spleen tyrosine kinase gene MP:0012080 chylous ascites IAGP N RGD:5509061 20141003 MGI PMID:7477352 731871 Syk spleen tyrosine kinase gene MP:0014404 decreased late pro-B cell number IAGP N RGD:5509061 20240405 MGI PMID:7477353 731873 Slc28a3 solute carrier family 28 (sodium-coupled nucleoside transporter), member 3 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 731873 Slc28a3 solute carrier family 28 (sodium-coupled nucleoside transporter), member 3 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 731873 Slc28a3 solute carrier family 28 (sodium-coupled nucleoside transporter), member 3 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 731875 Retsat retinol saturase (all trans retinol 13,14 reductase) gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20160721 MGI PMID:19940255 731875 Retsat retinol saturase (all trans retinol 13,14 reductase) gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20160721 MGI PMID:19940255 731875 Retsat retinol saturase (all trans retinol 13,14 reductase) gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20160721 MGI PMID:19940255 731875 Retsat retinol saturase (all trans retinol 13,14 reductase) gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20160721 MGI PMID:19940255 731875 Retsat retinol saturase (all trans retinol 13,14 reductase) gene MP:0011233 abnormal vitamin A metabolism IAGP N RGD:5509061 20160721 MGI PMID:19940255 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16720880 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20170831 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20180614 MGI PMID:29078393 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20230706 MGI PMID:27606604 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:11073884 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15070745 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16720880 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16730346 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:20713518 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15843414 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16720880 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:19411759 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20160218 MGI PMID:24748541 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:24142516 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20160929 MGI PMID:25787764 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170831 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15109497 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20160929 MGI PMID:25787764 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170831 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11784028 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:16514068 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20191003 MGI PMID:31147515 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20191107 MGI PMID:29183906 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20240808 MGI PMID:38474134 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:17868091 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20170831 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20191107 MGI PMID:29183906 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20211021 MGI PMID:29016838 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20141003 MGI PMID:11073884 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20141003 MGI PMID:19483677 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:20713518 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20150716 MGI PMID:25053429 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231123 MGI PMID:20018673 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:11784028 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000296 absent trabeculae carneae IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:19411759 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20240808 MGI PMID:38474134 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:11390666 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:16730346 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:23892084 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11390666 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20161216 MGI PMID:24120474 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15070745 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:22560297 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22560297 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:15175244 731878 Nkx2-5 NK2 homeobox 5 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240905 MGI PMID:36715298 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21177343 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17397913 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001575 cyanosis IAGP N RGD:5509061 20150716 MGI PMID:25053429 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001575 cyanosis IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11784028 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15109497 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001633 poor circulation IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16267821 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16730346 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21177343 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001785 edema IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:19411759 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:17397913 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20170831 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19411759 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20160218 MGI PMID:24748541 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20211021 MGI PMID:29016838 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20150716 MGI PMID:25053429 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23892084 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002083 premature death IAGP N RGD:5509061 20160929 MGI PMID:25787764 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002083 premature death IAGP N RGD:5509061 20170831 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11390666 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23184148 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23303524 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141120 MGI PMID:24812305 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002188 small heart IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002188 small heart IAGP N RGD:5509061 20240808 MGI PMID:38474134 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:24142516 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20150716 MGI PMID:25053429 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20191107 MGI PMID:29183906 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20211021 MGI PMID:29016838 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:17344228 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:15070745 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:15109497 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002234 abnormal pharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:11390666 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15070745 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15175244 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:17344228 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20150716 MGI PMID:25053429 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20230706 MGI PMID:27606604 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:22028467 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:24142516 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20160218 MGI PMID:24748541 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20170831 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20191003 MGI PMID:31147515 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20191107 MGI PMID:29183906 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20211021 MGI PMID:29016838 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15070745 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15175244 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15902305 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15843414 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:16720880 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15843414 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15109497 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15843414 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170831 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20180301 MGI PMID:28698371 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20160929 MGI PMID:25787764 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20180301 MGI PMID:28698371 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20240905 MGI PMID:36715298 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16720880 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:17344228 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:20713518 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:11390666 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:11784028 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20190509 MGI PMID:26226998 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:16720880 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15843414 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18178777 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:18084293 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16514068 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20160929 MGI PMID:25787764 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18178777 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003228 abnormal sinus venosus morphology IAGP N RGD:5509061 20141003 MGI PMID:11784028 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003228 abnormal sinus venosus morphology IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:21690310 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:21690310 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003547 abnormal pulmonary pressure IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15902305 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20150716 MGI PMID:25053429 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20211021 MGI PMID:29016838 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003872 absent heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:16720880 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003872 absent heart right ventricle IAGP N RGD:5509061 20150716 MGI PMID:25053429 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16720880 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:11073884 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:18084293 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20190509 MGI PMID:26226998 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003897 abnormal ST segment IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003898 abnormal QRS complex IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003901 abnormal PR interval IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003916 decreased heart left ventricle weight IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20150716 MGI PMID:25053429 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18178777 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11390666 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15902305 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16314491 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160218 MGI PMID:24748541 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004009 abnormal diastolic filling velocity IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:19411759 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004062 dilated heart right atrium IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004062 dilated heart right atrium IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004063 dilated heart left atrium IAGP N RGD:5509061 20231221 MGI PMID:15843414 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20191003 MGI PMID:31147515 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:21690310 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:20713518 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004092 absent Z line IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004093 diffuse Z line IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004114 abnormal atrioventricular node morphology IAGP N RGD:5509061 20141003 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004114 abnormal atrioventricular node morphology IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004114 abnormal atrioventricular node morphology IAGP N RGD:5509061 20190509 MGI PMID:26226998 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004117 abnormal atrioventricular bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15109497 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004123 abnormal impulse conducting system morphology IAGP N RGD:5509061 20141003 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004123 abnormal impulse conducting system morphology IAGP N RGD:5509061 20141003 MGI PMID:15109497 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004124 abnormal Purkinje fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004146 absent M line IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20160929 MGI PMID:25787764 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20180531 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004225 patent cardiac foramen ovale IAGP N RGD:5509061 20141003 MGI PMID:11073884 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004225 patent cardiac foramen ovale IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:18178777 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20191003 MGI PMID:31147515 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004555 pharynx hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11390666 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20160929 MGI PMID:25787764 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:15175244 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:16720880 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004937 dilated heart IAGP N RGD:5509061 20170831 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0004937 dilated heart IAGP N RGD:5509061 20180301 MGI PMID:28698371 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160929 MGI PMID:25787764 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11073884 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23571217 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20191003 MGI PMID:31147515 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:11390666 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:11784028 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:15070745 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:15902305 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16314491 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16730346 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:19411759 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11073884 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16314491 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17397913 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22028467 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24142516 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:22028467 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21690310 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18178777 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15109497 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20180301 MGI PMID:28698371 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20141003 MGI PMID:11390666 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11390666 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20161216 MGI PMID:24120474 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16314491 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141003 MGI PMID:11073884 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:11073884 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006123 tricuspid valve atresia IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:11784028 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:17344228 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20150716 MGI PMID:25053429 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20211021 MGI PMID:29016838 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231123 MGI PMID:20018673 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:11784028 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006141 abnormal atrioventricular node conduction IAGP N RGD:5509061 20141003 MGI PMID:18084293 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006141 abnormal atrioventricular node conduction IAGP N RGD:5509061 20190509 MGI PMID:26226998 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:11390666 731878 Nkx2-5 NK2 homeobox 5 gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0008727 increased heart right atrium size IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:15902305 731878 Nkx2-5 NK2 homeobox 5 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:16314491 731878 Nkx2-5 NK2 homeobox 5 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20231207 MGI PMID:33846290 731878 Nkx2-5 NK2 homeobox 5 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17008600 731878 Nkx2-5 NK2 homeobox 5 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17008600 731878 Nkx2-5 NK2 homeobox 5 gene MP:0009382 abnormal cardiac jelly morphology IAGP N RGD:5509061 20141003 MGI PMID:16314491 731878 Nkx2-5 NK2 homeobox 5 gene MP:0009844 abnormal neural crest cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17344228 731878 Nkx2-5 NK2 homeobox 5 gene MP:0009845 abnormal neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16720880 731878 Nkx2-5 NK2 homeobox 5 gene MP:0009861 abnormal pyloric sphincter morphology IAGP N RGD:5509061 20161216 MGI PMID:24120474 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:21690310 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20190509 MGI PMID:26226998 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19411759 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20713518 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20160218 MGI PMID:24748541 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20211021 MGI PMID:29016838 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20230706 MGI PMID:27606604 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231123 MGI PMID:20018673 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:11073884 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:15843414 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:19411759 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:19483677 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20230706 MGI PMID:27606604 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010405 ostium secundum atrial septal defect IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23892084 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010416 interventricular septum membranous part aneurysm IAGP N RGD:5509061 20170831 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15070745 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19483677 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20231130 MGI PMID:26299482 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15902305 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20150716 MGI PMID:25053429 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010424 double chambered heart right ventricle IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010432 common ventricle IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010432 common ventricle IAGP N RGD:5509061 20141003 MGI PMID:15902305 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010450 atrial septal aneurysm IAGP N RGD:5509061 20141003 MGI PMID:11073884 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010455 aortopulmonary window IAGP N RGD:5509061 20141003 MGI PMID:15070745 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010464 abnormal aortic arch and aortic arch branch attachment IAGP N RGD:5509061 20141003 MGI PMID:15070745 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20141003 MGI PMID:11073884 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010498 abnormal interventricular septum muscular part morphology IAGP N RGD:5509061 20170831 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010498 abnormal interventricular septum muscular part morphology IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:15109497 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20190509 MGI PMID:26226998 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010520 sinoatrial block IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010520 sinoatrial block IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010532 absent atrioventricular node IAGP N RGD:5509061 20231221 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010533 atrioventricular node hypoplasia IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010533 atrioventricular node hypoplasia IAGP N RGD:5509061 20231221 MGI PMID:15109497 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010536 Ebstein's malformation of tricuspid valve IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19411759 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20231123 MGI PMID:20018673 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010557 dilated pulmonary artery IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010559 heart block IAGP N RGD:5509061 20141003 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010566 abnormal left posterior bundle morphology IAGP N RGD:5509061 20190509 MGI PMID:26226998 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010571 shortened ST segment IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010571 shortened ST segment IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:15070745 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20150716 MGI PMID:25053429 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010587 conotruncal ridge hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15902305 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010587 conotruncal ridge hypoplasia IAGP N RGD:5509061 20231214 MGI PMID:15070745 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20141003 MGI PMID:11073884 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010614 abnormal mitral valve cusp morphology IAGP N RGD:5509061 20141003 MGI PMID:23892084 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010622 abnormal tricuspid valve cusp morphology IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010625 absent tricuspid valve cusps IAGP N RGD:5509061 20141003 MGI PMID:23892084 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010626 thick tricuspid valve cusps IAGP N RGD:5509061 20170831 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010634 increased QRS amplitude IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010636 bundle branch block IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010662 abnormal intersomitic artery morphology IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:20713518 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010759 decreased right ventricle systolic pressure IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010780 abnormal stomach smooth muscle circular layer morphology IAGP N RGD:5509061 20161216 MGI PMID:24120474 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010805 abnormal stomach smooth muscle outer longitudinal layer morphology IAGP N RGD:5509061 20161216 MGI PMID:24120474 731878 Nkx2-5 NK2 homeobox 5 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170831 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20713518 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20231130 MGI PMID:26299482 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23892084 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15109497 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16514068 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20190509 MGI PMID:25028484 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11390666 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11784028 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16267821 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16314491 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16720880 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16730346 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17397913 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22028467 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20150716 MGI PMID:25053429 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180614 MGI PMID:29078393 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20231123 MGI PMID:20018673 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15902305 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411759 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23571217 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180503 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20191107 MGI PMID:29183906 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20211021 MGI PMID:29016838 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15070745 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15843414 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011262 abnormal pharyngeal arch mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:16720880 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011263 abnormal spleen mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:22560297 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:16267821 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011390 abnormal fetal cardiomyocyte physiology IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011394 increased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20713518 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011394 increased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20160929 MGI PMID:25787764 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20240321 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231130 MGI PMID:26299482 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:15070745 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011928 abnormal mitral valve flow IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:21690310 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0011953 prolonged PQ interval IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20190418 MGI PMID:28302382 731878 Nkx2-5 NK2 homeobox 5 gene MP:0012179 abnormal splanchnic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16720880 731878 Nkx2-5 NK2 homeobox 5 gene MP:0012270 cardiac edema IAGP N RGD:5509061 20141003 MGI PMID:16730346 731878 Nkx2-5 NK2 homeobox 5 gene MP:0012270 cardiac edema IAGP N RGD:5509061 20211021 MGI PMID:29016838 731878 Nkx2-5 NK2 homeobox 5 gene MP:0012492 pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10021345 731878 Nkx2-5 NK2 homeobox 5 gene MP:0012515 abnormal heart apex morphology IAGP N RGD:5509061 20161229 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0012515 abnormal heart apex morphology IAGP N RGD:5509061 20170413 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0012556 increased cell death IAGP N RGD:5509061 20211021 MGI PMID:29016838 731878 Nkx2-5 NK2 homeobox 5 gene MP:0012624 decreased acetylcholinesterase activity IAGP N RGD:5509061 20190509 MGI PMID:26226998 731878 Nkx2-5 NK2 homeobox 5 gene MP:0014044 absent cardiac outflow tract IAGP N RGD:5509061 20160304 MGI PMID:16720880 731878 Nkx2-5 NK2 homeobox 5 gene MP:0014072 decreased cardiac muscle glycogen level IAGP N RGD:5509061 20191226 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0014519 myocardial ventricular hypertrabeculation IAGP N RGD:5509061 20240822 MGI PMID:15109497 731878 Nkx2-5 NK2 homeobox 5 gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20170831 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231221 MGI PMID:15843414 731878 Nkx2-5 NK2 homeobox 5 gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20240808 MGI PMID:38474134 731878 Nkx2-5 NK2 homeobox 5 gene MP:0030340 absent fourth pharyngeal arch artery IAGP N RGD:5509061 20171116 MGI PMID:15175244 731878 Nkx2-5 NK2 homeobox 5 gene MP:0030341 fourth pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20171116 MGI PMID:15175244 731878 Nkx2-5 NK2 homeobox 5 gene MP:0030564 thick myocardium compact layer IAGP N RGD:5509061 20180524 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0030566 abnormal A band morphology IAGP N RGD:5509061 20180531 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0030567 abnormal I band morphology IAGP N RGD:5509061 20180531 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0030568 abnormal H zone morphology IAGP N RGD:5509061 20180531 MGI PMID:26526197 731878 Nkx2-5 NK2 homeobox 5 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20191128 MGI PMID:15902305 731878 Nkx2-5 NK2 homeobox 5 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20240125 MGI PMID:33846290 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:15843414 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031147 abnormal ventricular thrombosis IAGP N RGD:5509061 20201210 MGI PMID:24938781 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031166 abnormal aortic valve commissure morphology IAGP N RGD:5509061 20210506 MGI PMID:11073884 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031525 thin left ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:29016838 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031530 abnormal heart ventricle shape IAGP N RGD:5509061 20240104 MGI PMID:15085192 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031530 abnormal heart ventricle shape IAGP N RGD:5509061 20240104 MGI PMID:7628699 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031536 decreased heart atrium wall thickness IAGP N RGD:5509061 20240808 MGI PMID:38474134 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031583 semilunar valve hypoplasia IAGP N RGD:5509061 20240125 MGI PMID:15070745 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031607 abnormal fetal cardiomyocyte mitochondrial morphology IAGP N RGD:5509061 20240321 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031608 decreased fetal cardiomyocyte size IAGP N RGD:5509061 20240321 MGI PMID:18854137 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031608 decreased fetal cardiomyocyte size IAGP N RGD:5509061 20240808 MGI PMID:38474134 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031609 increased fetal cardiomyocyte size IAGP N RGD:5509061 20240321 MGI PMID:34333993 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031611 decreased fetal cardiomyocyte number IAGP N RGD:5509061 20240321 MGI PMID:25953344 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15843414 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:28352650 731878 Nkx2-5 NK2 homeobox 5 gene MP:0031634 decreased heart right ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:28352650 731879 Plscr1 phospholipid scramblase 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12010804 731879 Plscr1 phospholipid scramblase 1 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:12010804 731879 Plscr1 phospholipid scramblase 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 731879 Plscr1 phospholipid scramblase 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12010804 731879 Plscr1 phospholipid scramblase 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15328404 731879 Plscr1 phospholipid scramblase 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15328404 731879 Plscr1 phospholipid scramblase 1 gene MP:0002415 abnormal neutrophil differentiation IAGP N RGD:5509061 20141003 MGI PMID:12010804 731879 Plscr1 phospholipid scramblase 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20211021 MGI 731879 Plscr1 phospholipid scramblase 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15328404 731879 Plscr1 phospholipid scramblase 1 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15328404 731879 Plscr1 phospholipid scramblase 1 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:15328404 731879 Plscr1 phospholipid scramblase 1 gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:12010804 731879 Plscr1 phospholipid scramblase 1 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20210128 MGI 731879 Plscr1 phospholipid scramblase 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 731882 Nudt1 nudix hydrolase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23143307 731882 Nudt1 nudix hydrolase 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23143307 731882 Nudt1 nudix hydrolase 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11572992 731882 Nudt1 nudix hydrolase 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11572992 731882 Nudt1 nudix hydrolase 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:23143307 731882 Nudt1 nudix hydrolase 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:23143307 731882 Nudt1 nudix hydrolase 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:23143307 731882 Nudt1 nudix hydrolase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12531017 731882 Nudt1 nudix hydrolase 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11572992 731882 Nudt1 nudix hydrolase 1 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:23143307 731882 Nudt1 nudix hydrolase 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23143307 731882 Nudt1 nudix hydrolase 1 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11572992 731882 Nudt1 nudix hydrolase 1 gene MP:0010947 abnormal single-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:23143307 731884 Abi1 abl interactor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21482783 731884 Abi1 abl interactor 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21482783 731884 Abi1 abl interactor 1 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:21482783 731884 Abi1 abl interactor 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:21482783 731884 Abi1 abl interactor 1 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0003057 abnormal epicardium morphology IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21482783 731884 Abi1 abl interactor 1 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:21482783 731884 Abi1 abl interactor 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16401422 731884 Abi1 abl interactor 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:16401422 731884 Abi1 abl interactor 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0010395 abnormal pharyngeal arch development IAGP N RGD:5509061 20141003 MGI PMID:21482783 731884 Abi1 abl interactor 1 gene MP:0010545 abnormal heart layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16401422 731884 Abi1 abl interactor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21482783 731884 Abi1 abl interactor 1 gene MP:0012095 increased Reichert's membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:21173240 731884 Abi1 abl interactor 1 gene MP:0012270 cardiac edema IAGP N RGD:5509061 20141003 MGI PMID:21482783 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:20684022 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16939396 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20170209 MGI PMID:25716980 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20160818 MGI PMID:22991301 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:20684022 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220303 MGI PMID:24853953 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19129368 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17599069 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001147 small testis IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001147 small testis IAGP N RGD:5509061 20220303 MGI PMID:24853953 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001147 small testis IAGP N RGD:5509061 20220324 MGI PMID:29293683 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:15486564 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:15486564 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20230316 MGI PMID:27065197 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220324 MGI PMID:29293683 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220324 MGI PMID:29293683 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16939396 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7550313 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20191107 MGI PMID:30867511 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15486564 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220303 MGI PMID:24853953 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:21892189 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15215868 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17599069 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001925 male infertility IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001925 male infertility IAGP N RGD:5509061 20230316 MGI PMID:27065197 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15215868 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15486564 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17599069 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:17599069 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220303 MGI PMID:24853953 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17599069 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:7550313 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:7550313 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:17599069 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220303 MGI PMID:24853953 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220303 MGI PMID:24853953 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20220324 MGI PMID:29293683 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220303 MGI PMID:24853953 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15486564 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220303 MGI PMID:24853953 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230316 MGI PMID:27065197 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:15486564 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20160818 MGI PMID:22991301 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20684022 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:10932192 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:17539739 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:19151073 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:22527485 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0003674 oxidative stress IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:21892189 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:17540358 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0003933 abnormal cementum morphology IAGP N RGD:5509061 20160818 MGI PMID:22991301 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20160818 MGI PMID:22991301 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20170209 MGI PMID:25716980 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:20684022 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20220303 MGI PMID:24853953 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15215868 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220303 MGI PMID:24853953 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220324 MGI PMID:29293683 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230316 MGI PMID:27065197 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:17540358 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:17599069 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220324 MGI PMID:29293683 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20170209 MGI PMID:25716980 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:16939396 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:15215868 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:17599069 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0005159 azoospermia IAGP N RGD:5509061 20220324 MGI PMID:29293683 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:17599069 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:17599069 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23133398 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:17540358 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20220324 MGI PMID:29293683 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17599069 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:15486564 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:23022299 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20191107 MGI PMID:30867511 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21659337 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21892189 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220303 MGI PMID:24853953 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220303 MGI PMID:24853953 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0009246 pale spleen IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20170209 MGI PMID:25716980 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:21659337 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7550313 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:21659337 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:19129368 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20191107 MGI PMID:30867511 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20170209 MGI PMID:25716980 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20220922 MGI PMID:16939396 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16939396 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21659337 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7550313 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20684022 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20684022 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:15486564 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0011165 abnormal tooth root development IAGP N RGD:5509061 20160818 MGI PMID:22991301 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0011411 abnormal gonadal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:15486564 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0011585 decreased alkaline phosphatase activity IAGP N RGD:5509061 20170209 MGI PMID:25716980 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0011594 decreased catalase activity IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20211209 MGI PMID:30998386 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220303 MGI PMID:24853953 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220324 MGI PMID:29293683 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:20684022 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:20684022 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160818 MGI PMID:22991301 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20170209 MGI PMID:25716980 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20220922 MGI PMID:16939396 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0020138 delayed bone mineralization IAGP N RGD:5509061 20170209 MGI PMID:25716980 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0021189 increased bone mineral density of presacral vertebrae IAGP N RGD:5509061 20220922 MGI PMID:16939396 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0021191 increased bone mineral density of lumbar vertebrae IAGP N RGD:5509061 20220922 MGI PMID:16939396 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0030281 thin parietal bone IAGP N RGD:5509061 20171102 MGI PMID:9056646 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0030451 abnormal dentin mineralization IAGP N RGD:5509061 20171221 MGI PMID:22991301 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0030452 abnormal cementum mineralization IAGP N RGD:5509061 20171221 MGI PMID:25716980 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0030453 abnormal odontoblast morphology IAGP N RGD:5509061 20171221 MGI PMID:22991301 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0030493 abnormal tooth root morphology IAGP N RGD:5509061 20171228 MGI PMID:22991301 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0030497 short tooth root IAGP N RGD:5509061 20171228 MGI PMID:22991301 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0030545 abnormal acellular cementum morphology IAGP N RGD:5509061 20180208 MGI PMID:25716980 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0030546 abnormal cellular cementum morphology IAGP N RGD:5509061 20180208 MGI PMID:25716980 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0030562 enlarged dental pulp chamber IAGP N RGD:5509061 20191219 MGI PMID:22991301 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0030935 increased primordial germ cell apoptosis IAGP N RGD:5509061 20190411 MGI PMID:23022299 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20220303 MGI PMID:24853953 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220303 MGI PMID:24853953 731885 Alpl alkaline phosphatase, liver/bone/kidney gene MP:0031355 abnormal proacrosomal vesicle fusion IAGP N RGD:5509061 20220303 MGI PMID:24853953 731888 Parva parvin, alpha gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 731888 Parva parvin, alpha gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 731888 Parva parvin, alpha gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:19829382 731888 Parva parvin, alpha gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:19829382 731888 Parva parvin, alpha gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 731888 Parva parvin, alpha gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 731888 Parva parvin, alpha gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 731888 Parva parvin, alpha gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20230601 MGI 731888 Parva parvin, alpha gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230601 MGI 731888 Parva parvin, alpha gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 731888 Parva parvin, alpha gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0003279 aneurysm IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19829382 731888 Parva parvin, alpha gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 731888 Parva parvin, alpha gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0011738 anasarca IAGP N RGD:5509061 20240404 MGI PMID:19798050 731888 Parva parvin, alpha gene MP:0031613 fetal cardiomyocyte disarray IAGP N RGD:5509061 20240404 MGI PMID:19798050 731890 Cdk1 cyclin dependent kinase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20181025 MGI PMID:28723571 731890 Cdk1 cyclin dependent kinase 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220623 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20220623 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20181025 MGI PMID:28723571 731890 Cdk1 cyclin dependent kinase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141127 MGI PMID:25139855 731890 Cdk1 cyclin dependent kinase 1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141127 MGI PMID:25139855 731890 Cdk1 cyclin dependent kinase 1 gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0003706 abnormal cell nucleus count IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20181025 MGI PMID:28723571 731890 Cdk1 cyclin dependent kinase 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141127 MGI PMID:25139855 731890 Cdk1 cyclin dependent kinase 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20181025 MGI PMID:28723571 731890 Cdk1 cyclin dependent kinase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22355113 731890 Cdk1 cyclin dependent kinase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20181025 MGI PMID:28723571 731890 Cdk1 cyclin dependent kinase 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17700700 731890 Cdk1 cyclin dependent kinase 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18787066 731890 Cdk1 cyclin dependent kinase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17700700 731890 Cdk1 cyclin dependent kinase 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20181025 MGI PMID:28723571 731890 Cdk1 cyclin dependent kinase 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:18787066 731893 Atp6v0c ATPase, H+ transporting, lysosomal V0 subunit C gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11112332 731893 Atp6v0c ATPase, H+ transporting, lysosomal V0 subunit C gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:11112332 731893 Atp6v0c ATPase, H+ transporting, lysosomal V0 subunit C gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:11112332 731893 Atp6v0c ATPase, H+ transporting, lysosomal V0 subunit C gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10556625 731898 Rnf138 ring finger protein 138 gene MP:0001147 small testis IAGP N RGD:5509061 20211230 MGI PMID:28518149 731898 Rnf138 ring finger protein 138 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20211230 MGI PMID:28518149 731898 Rnf138 ring finger protein 138 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20211230 MGI PMID:28518149 731898 Rnf138 ring finger protein 138 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20211230 MGI PMID:28518149 731898 Rnf138 ring finger protein 138 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20211230 MGI PMID:28518149 731898 Rnf138 ring finger protein 138 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20211230 MGI PMID:28518149 731898 Rnf138 ring finger protein 138 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20211230 MGI PMID:28518149 731898 Rnf138 ring finger protein 138 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20211230 MGI PMID:28518149 731898 Rnf138 ring finger protein 138 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20211230 MGI PMID:28518149 731898 Rnf138 ring finger protein 138 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20211230 MGI PMID:28518149 731898 Rnf138 ring finger protein 138 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20211230 MGI PMID:28518149 731899 Macrod1 mono-ADP ribosylhydrolase 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 731899 Macrod1 mono-ADP ribosylhydrolase 1 gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 731901 Spata19 spermatogenesis associated 19 gene MP:0001925 male infertility IAGP N RGD:5509061 20210325 MGI PMID:26265198 731901 Spata19 spermatogenesis associated 19 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20210325 MGI PMID:26265198 731901 Spata19 spermatogenesis associated 19 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20210325 MGI PMID:26265198 731901 Spata19 spermatogenesis associated 19 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20210325 MGI PMID:26265198 731901 Spata19 spermatogenesis associated 19 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:26265198 731901 Spata19 spermatogenesis associated 19 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20210325 MGI PMID:26265198 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15539485 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9590175 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:15539485 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:9590175 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15539485 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9590175 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:12814946 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15539485 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:9590175 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:12062105 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14551157 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:14670843 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:10880048 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:16126817 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19590036 731911 Mmp9 matrix metallopeptidase 9 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:16495447 731911 Mmp9 matrix metallopeptidase 9 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:16500946 731911 Mmp9 matrix metallopeptidase 9 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11081634 731911 Mmp9 matrix metallopeptidase 9 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19074147 731911 Mmp9 matrix metallopeptidase 9 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15539485 731911 Mmp9 matrix metallopeptidase 9 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:10411111 731911 Mmp9 matrix metallopeptidase 9 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18676849 731911 Mmp9 matrix metallopeptidase 9 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16481424 731911 Mmp9 matrix metallopeptidase 9 gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12062105 731911 Mmp9 matrix metallopeptidase 9 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12062105 731911 Mmp9 matrix metallopeptidase 9 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19590036 731911 Mmp9 matrix metallopeptidase 9 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:18332263 731911 Mmp9 matrix metallopeptidase 9 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12847275 731911 Mmp9 matrix metallopeptidase 9 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:10974013 731911 Mmp9 matrix metallopeptidase 9 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10974013 731911 Mmp9 matrix metallopeptidase 9 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11081634 731911 Mmp9 matrix metallopeptidase 9 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16397239 731911 Mmp9 matrix metallopeptidase 9 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19401296 731911 Mmp9 matrix metallopeptidase 9 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19401296 731911 Mmp9 matrix metallopeptidase 9 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12847275 731911 Mmp9 matrix metallopeptidase 9 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:19364840 731911 Mmp9 matrix metallopeptidase 9 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16344067 731911 Mmp9 matrix metallopeptidase 9 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12847275 731911 Mmp9 matrix metallopeptidase 9 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:10880400 731911 Mmp9 matrix metallopeptidase 9 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:9590175 731911 Mmp9 matrix metallopeptidase 9 gene MP:0002839 increased susceptibility to dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:18332263 731911 Mmp9 matrix metallopeptidase 9 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:19590036 731911 Mmp9 matrix metallopeptidase 9 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:19364840 731911 Mmp9 matrix metallopeptidase 9 gene MP:0002936 joint swelling IAGP N RGD:5509061 20141003 MGI PMID:19364840 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:12031700 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:18264108 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9590175 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:16684893 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9590175 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:9590175 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:18332263 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18332263 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15699164 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15539485 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:9590175 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003434 decreased susceptibility to induced choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:14563686 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:19364840 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:18676849 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:16397239 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:18676849 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17484881 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:19074147 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:16126817 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15746435 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:15746435 731911 Mmp9 matrix metallopeptidase 9 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:19401296 731911 Mmp9 matrix metallopeptidase 9 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:18332263 731911 Mmp9 matrix metallopeptidase 9 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:12814946 731911 Mmp9 matrix metallopeptidase 9 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:9590175 731911 Mmp9 matrix metallopeptidase 9 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:10587514 731911 Mmp9 matrix metallopeptidase 9 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12062105 731911 Mmp9 matrix metallopeptidase 9 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:12411401 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:12581831 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18332263 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:10995849 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:11350822 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:12354772 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:18264108 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:19443702 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:9687525 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15746435 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11970978 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:12411401 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:14551157 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005600 increased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16126817 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16126817 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19590036 731911 Mmp9 matrix metallopeptidase 9 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10359808 731911 Mmp9 matrix metallopeptidase 9 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:11129784 731911 Mmp9 matrix metallopeptidase 9 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12354772 731911 Mmp9 matrix metallopeptidase 9 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19590036 731911 Mmp9 matrix metallopeptidase 9 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:12814946 731911 Mmp9 matrix metallopeptidase 9 gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15539485 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:12847275 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008160 increased diameter of humerus IAGP N RGD:5509061 20141003 MGI PMID:12814946 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:16344067 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17362932 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20141003 MGI PMID:18332263 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:18332263 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:10359808 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:12847275 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:14764732 731911 Mmp9 matrix metallopeptidase 9 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12847275 731911 Mmp9 matrix metallopeptidase 9 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12062105 731911 Mmp9 matrix metallopeptidase 9 gene MP:0009427 increased tibialis anterior weight IAGP N RGD:5509061 20141003 MGI PMID:19074147 731911 Mmp9 matrix metallopeptidase 9 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16481424 731911 Mmp9 matrix metallopeptidase 9 gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11081634 731911 Mmp9 matrix metallopeptidase 9 gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:12368215 731911 Mmp9 matrix metallopeptidase 9 gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11081634 731911 Mmp9 matrix metallopeptidase 9 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12062105 731911 Mmp9 matrix metallopeptidase 9 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16344067 731911 Mmp9 matrix metallopeptidase 9 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:16495447 731911 Mmp9 matrix metallopeptidase 9 gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:16684893 731911 Mmp9 matrix metallopeptidase 9 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18676849 731911 Mmp9 matrix metallopeptidase 9 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:18332263 731911 Mmp9 matrix metallopeptidase 9 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:10880400 731911 Mmp9 matrix metallopeptidase 9 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:10880400 731911 Mmp9 matrix metallopeptidase 9 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:18332263 731911 Mmp9 matrix metallopeptidase 9 gene MP:0020944 decreased susceptibility to Flaviviridae infection IAGP N RGD:5509061 20200430 MGI PMID:18632868 731911 Mmp9 matrix metallopeptidase 9 gene MP:0021161 increased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:18332263 731911 Mmp9 matrix metallopeptidase 9 gene MP:0030756 decreased histamine level IAGP N RGD:5509061 20180927 MGI PMID:16684893 731911 Mmp9 matrix metallopeptidase 9 gene MP:0031040 increased susceptibility to Picornaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:18332263 731911 Mmp9 matrix metallopeptidase 9 gene MP:0031043 decreased susceptibility to Flaviviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:18632868 731911 Mmp9 matrix metallopeptidase 9 gene MP:0031273 decreased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:10841523 731911 Mmp9 matrix metallopeptidase 9 gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:19401296 731911 Mmp9 matrix metallopeptidase 9 gene MP:0031385 enhanced blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:18632868 731913 Cavin3 caveolae associated 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24069528 731913 Cavin3 caveolae associated 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24069528 731913 Cavin3 caveolae associated 3 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20231207 MGI 731913 Cavin3 caveolae associated 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:24069528 731913 Cavin3 caveolae associated 3 gene MP:0003180 abnormal pulmonary endothelial cell surface IAGP N RGD:5509061 20141003 MGI PMID:23652019 731913 Cavin3 caveolae associated 3 gene MP:0003950 abnormal plasma membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:23652019 731913 Cavin3 caveolae associated 3 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:24069528 731913 Cavin3 caveolae associated 3 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 731913 Cavin3 caveolae associated 3 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23652019 731913 Cavin3 caveolae associated 3 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 731913 Cavin3 caveolae associated 3 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:24069528 731913 Cavin3 caveolae associated 3 gene MP:0011174 lipodystrophy IAGP N RGD:5509061 20141003 MGI PMID:24069528 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11752462 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:11752462 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20141003 MGI PMID:11752462 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11752462 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11752462 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:11076932 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11076932 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0001908 abnormal somatosensory cortex physiology IAGP N RGD:5509061 20141003 MGI PMID:11752462 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11076932 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11095717 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11095717 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11752462 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:11752462 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:11752462 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:11752462 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:11752462 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:11095717 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11752462 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:11752462 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:11752462 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0011231 abnormal vitamin E level IAGP N RGD:5509061 20141003 MGI PMID:11076932 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0011231 abnormal vitamin E level IAGP N RGD:5509061 20141003 MGI PMID:11095717 731915 Ttpa tocopherol (alpha) transfer protein gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:11752462 731916 Pdlim4 PDZ and LIM domain 4 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20230601 MGI 731916 Pdlim4 PDZ and LIM domain 4 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 731916 Pdlim4 PDZ and LIM domain 4 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20230601 MGI 731916 Pdlim4 PDZ and LIM domain 4 gene MP:0002764 short tibia IEA N RGD:5509061 20230601 MGI 731916 Pdlim4 PDZ and LIM domain 4 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20230601 MGI 731916 Pdlim4 PDZ and LIM domain 4 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 731916 Pdlim4 PDZ and LIM domain 4 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20230601 MGI 731916 Pdlim4 PDZ and LIM domain 4 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230601 MGI 731918 Spon2 spondin 2, extracellular matrix protein gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:14691481 731918 Spon2 spondin 2, extracellular matrix protein gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:14691481 731918 Spon2 spondin 2, extracellular matrix protein gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:14691481 731919 Car5a carbonic anhydrase 5a, mitochondrial gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23589845 731919 Car5a carbonic anhydrase 5a, mitochondrial gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23589845 731919 Car5a carbonic anhydrase 5a, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23589845 731919 Car5a carbonic anhydrase 5a, mitochondrial gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22109883 731919 Car5a carbonic anhydrase 5a, mitochondrial gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:23589845 731919 Car5a carbonic anhydrase 5a, mitochondrial gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23589845 731919 Car5a carbonic anhydrase 5a, mitochondrial gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23589845 731920 Tob1 transducer of ErbB-2.1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11163184 731920 Tob1 transducer of ErbB-2.1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:11163184 731920 Tob1 transducer of ErbB-2.1 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:11163184 731920 Tob1 transducer of ErbB-2.1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11163184 731920 Tob1 transducer of ErbB-2.1 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:11163184 731920 Tob1 transducer of ErbB-2.1 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:11163184 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:16026768 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16026768 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17432963 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16026768 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16026768 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17432963 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16026768 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16026768 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:16026768 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16026768 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17432963 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:16026768 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:16026768 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:17432963 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:16026768 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:17432963 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16026768 731926 Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10 gene MP:0021009 abnormal synaptic physiology IAGP N RGD:5509061 20210805 MGI PMID:17432963 731927 Mepe matrix extracellular phosphoglycoprotein with ASARM motif (bone) gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12421822 731927 Mepe matrix extracellular phosphoglycoprotein with ASARM motif (bone) gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:12421822 731927 Mepe matrix extracellular phosphoglycoprotein with ASARM motif (bone) gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20171221 MGI PMID:12421822 731927 Mepe matrix extracellular phosphoglycoprotein with ASARM motif (bone) gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20171221 MGI PMID:12421822 731927 Mepe matrix extracellular phosphoglycoprotein with ASARM motif (bone) gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20171221 MGI PMID:12421822 731927 Mepe matrix extracellular phosphoglycoprotein with ASARM motif (bone) gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:12421822 731930 Fyn Fyn proto-oncogene gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19668367 731930 Fyn Fyn proto-oncogene gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8562954 731930 Fyn Fyn proto-oncogene gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:8934570 731930 Fyn Fyn proto-oncogene gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:11245687 731930 Fyn Fyn proto-oncogene gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:15073522 731930 Fyn Fyn proto-oncogene gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:9114065 731930 Fyn Fyn proto-oncogene gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:1361685 731930 Fyn Fyn proto-oncogene gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:9114065 731930 Fyn Fyn proto-oncogene gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8264796 731930 Fyn Fyn proto-oncogene gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:8264796 731930 Fyn Fyn proto-oncogene gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:10869499 731930 Fyn Fyn proto-oncogene gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15073522 731930 Fyn Fyn proto-oncogene gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:11245687 731930 Fyn Fyn proto-oncogene gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:7509042 731930 Fyn Fyn proto-oncogene gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:11751285 731930 Fyn Fyn proto-oncogene gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220630 MGI PMID:21918125 731930 Fyn Fyn proto-oncogene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11245687 731930 Fyn Fyn proto-oncogene gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:15154672 731930 Fyn Fyn proto-oncogene gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:15154672 731930 Fyn Fyn proto-oncogene gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:8264796 731930 Fyn Fyn proto-oncogene gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:1361685 731930 Fyn Fyn proto-oncogene gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:1361685 731930 Fyn Fyn proto-oncogene gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:9114065 731930 Fyn Fyn proto-oncogene gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20141003 MGI PMID:11834300 731930 Fyn Fyn proto-oncogene gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:7723633 731930 Fyn Fyn proto-oncogene gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12563261 731930 Fyn Fyn proto-oncogene gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:1387588 731930 Fyn Fyn proto-oncogene gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8934569 731930 Fyn Fyn proto-oncogene gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8934570 731930 Fyn Fyn proto-oncogene gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8934569 731930 Fyn Fyn proto-oncogene gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8934570 731930 Fyn Fyn proto-oncogene gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:1516132 731930 Fyn Fyn proto-oncogene gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:11834300 731930 Fyn Fyn proto-oncogene gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220630 MGI PMID:21918125 731930 Fyn Fyn proto-oncogene gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:15154672 731930 Fyn Fyn proto-oncogene gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:10489260 731930 Fyn Fyn proto-oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10489260 731930 Fyn Fyn proto-oncogene gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12563261 731930 Fyn Fyn proto-oncogene gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8562954 731930 Fyn Fyn proto-oncogene gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11751285 731930 Fyn Fyn proto-oncogene gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:1387588 731930 Fyn Fyn proto-oncogene gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12239221 731930 Fyn Fyn proto-oncogene gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20141003 MGI PMID:11306441 731930 Fyn Fyn proto-oncogene gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11306441 731930 Fyn Fyn proto-oncogene gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:15539156 731930 Fyn Fyn proto-oncogene gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:1387588 731930 Fyn Fyn proto-oncogene gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20220630 MGI PMID:21918125 731930 Fyn Fyn proto-oncogene gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11751285 731930 Fyn Fyn proto-oncogene gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220630 MGI PMID:21918125 731930 Fyn Fyn proto-oncogene gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:10489260 731930 Fyn Fyn proto-oncogene gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:9381182 731930 Fyn Fyn proto-oncogene gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15902435 731930 Fyn Fyn proto-oncogene gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:11834300 731930 Fyn Fyn proto-oncogene gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:7877449 731930 Fyn Fyn proto-oncogene gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:8934570 731930 Fyn Fyn proto-oncogene gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:1387588 731930 Fyn Fyn proto-oncogene gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:1516132 731930 Fyn Fyn proto-oncogene gene MP:0003999 enhanced passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:7877449 731930 Fyn Fyn proto-oncogene gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20220630 MGI PMID:21918125 731930 Fyn Fyn proto-oncogene gene MP:0004821 increased susceptibility to experimental autoimmune uveoretinitis IAGP N RGD:5509061 20141003 MGI PMID:15902435 731930 Fyn Fyn proto-oncogene gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11751285 731930 Fyn Fyn proto-oncogene gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20220630 MGI PMID:21918125 731930 Fyn Fyn proto-oncogene gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19668367 731930 Fyn Fyn proto-oncogene gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19668367 731930 Fyn Fyn proto-oncogene gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19668367 731930 Fyn Fyn proto-oncogene gene MP:0005002 abnormal T cell clonal deletion IAGP N RGD:5509061 20141003 MGI PMID:1387588 731930 Fyn Fyn proto-oncogene gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19668367 731930 Fyn Fyn proto-oncogene gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563261 731930 Fyn Fyn proto-oncogene gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8934569 731930 Fyn Fyn proto-oncogene gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8562954 731930 Fyn Fyn proto-oncogene gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8934570 731930 Fyn Fyn proto-oncogene gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15539156 731930 Fyn Fyn proto-oncogene gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:1387588 731930 Fyn Fyn proto-oncogene gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:1516132 731930 Fyn Fyn proto-oncogene gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19668367 731930 Fyn Fyn proto-oncogene gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15539156 731930 Fyn Fyn proto-oncogene gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20220630 MGI PMID:21918125 731930 Fyn Fyn proto-oncogene gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11306441 731930 Fyn Fyn proto-oncogene gene MP:0008038 abnormal NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:8934570 731930 Fyn Fyn proto-oncogene gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:8934569 731930 Fyn Fyn proto-oncogene gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563261 731930 Fyn Fyn proto-oncogene gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563261 731930 Fyn Fyn proto-oncogene gene MP:0008233 abnormal pro-B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12563261 731930 Fyn Fyn proto-oncogene gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:1361685 731930 Fyn Fyn proto-oncogene gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:9114065 731930 Fyn Fyn proto-oncogene gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8934569 731930 Fyn Fyn proto-oncogene gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:8934570 731930 Fyn Fyn proto-oncogene gene MP:0008351 decreased gamma-delta intraepithelial T cell number IAGP N RGD:5509061 20141003 MGI PMID:9045930 731930 Fyn Fyn proto-oncogene gene MP:0008399 abnormal alpha-beta intraepithelial T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9045930 731930 Fyn Fyn proto-oncogene gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:1387588 731930 Fyn Fyn proto-oncogene gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15902435 731930 Fyn Fyn proto-oncogene gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22683124 731930 Fyn Fyn proto-oncogene gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:15902435 731930 Fyn Fyn proto-oncogene gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:11306441 731930 Fyn Fyn proto-oncogene gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:1387588 731930 Fyn Fyn proto-oncogene gene MP:0008698 abnormal interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:11306441 731930 Fyn Fyn proto-oncogene gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:11306441 731930 Fyn Fyn proto-oncogene gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:12239221 731930 Fyn Fyn proto-oncogene gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220630 MGI PMID:21918125 731930 Fyn Fyn proto-oncogene gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220630 MGI PMID:21918125 731930 Fyn Fyn proto-oncogene gene MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:9381182 731930 Fyn Fyn proto-oncogene gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15154672 731930 Fyn Fyn proto-oncogene gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20220630 MGI PMID:21918125 731930 Fyn Fyn proto-oncogene gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1361685 731930 Fyn Fyn proto-oncogene gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9114065 731930 Fyn Fyn proto-oncogene gene MP:0009970 increased hippocampus pyramidal cell number IAGP N RGD:5509061 20141003 MGI PMID:1361685 731930 Fyn Fyn proto-oncogene gene MP:0010011 ectopic hippocampus pyramidal cells IAGP N RGD:5509061 20141003 MGI PMID:9114065 731930 Fyn Fyn proto-oncogene gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:11834300 731930 Fyn Fyn proto-oncogene gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22683124 731930 Fyn Fyn proto-oncogene gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7958873 731930 Fyn Fyn proto-oncogene gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731930 Fyn Fyn proto-oncogene gene MP:0013286 abnormal sperm capacitation IAGP N RGD:5509061 20220630 MGI PMID:21918125 731930 Fyn Fyn proto-oncogene gene MP:0013585 thymus cortex atrophy IAGP N RGD:5509061 20150319 MGI PMID:8562954 731930 Fyn Fyn proto-oncogene gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:10869499 731930 Fyn Fyn proto-oncogene gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20171012 MGI PMID:10869499 731930 Fyn Fyn proto-oncogene gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20220630 MGI PMID:21918125 731930 Fyn Fyn proto-oncogene gene MP:0031389 abnormal ectoplasmic specialization morphology IAGP N RGD:5509061 20220428 MGI PMID:11751285 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:12019206 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:12019206 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:12019206 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12019206 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20230601 MGI PMID:30135927 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12019206 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12019206 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:12019206 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:12019206 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:1532662 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:1532662 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16959610 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16959610 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:12019206 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12019206 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:12019206 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:1532662 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:12019206 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:1532662 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:16959610 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:12019206 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0014063 Lafora bodies IAGP N RGD:5509061 20160304 MGI PMID:12019206 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0014063 Lafora bodies IAGP N RGD:5509061 20160304 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0014063 Lafora bodies IAGP N RGD:5509061 20160304 MGI PMID:22186026 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0014063 Lafora bodies IAGP N RGD:5509061 20230601 MGI PMID:30135927 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20160310 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20160407 MGI PMID:21493628 731931 Epm2a epilepsy, progressive myoclonic epilepsy, type 2 gene alpha gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:21493628 731935 Tbkbp1 TBK1 binding protein 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 731935 Tbkbp1 TBK1 binding protein 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23610142 731935 Tbkbp1 TBK1 binding protein 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 731935 Tbkbp1 TBK1 binding protein 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23610142 731935 Tbkbp1 TBK1 binding protein 1 gene MP:0008563 decreased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:23610142 731935 Tbkbp1 TBK1 binding protein 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:23610142 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20170105 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20160421 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20220811 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20220811 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20220811 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0004156 abnormal QT variability IEA N RGD:5509061 20220811 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0004924 abnormal behavior IEA N RGD:5509061 20240627 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0005036 diarrhea IAGP N RGD:5509061 20180215 MGI PMID:28137860 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220811 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20220811 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20180215 MGI PMID:28137860 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180215 MGI PMID:28137860 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20180215 MGI PMID:28137860 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20180215 MGI PMID:28137860 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20180215 MGI PMID:28137860 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160421 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0010062 decreased creatine level IAGP N RGD:5509061 20180215 MGI PMID:28137860 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20160421 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20180215 MGI PMID:28137860 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20220519 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20220811 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220811 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20220811 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0011468 abnormal urine amino acid level IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0011940 decreased food intake IEA N RGD:5509061 20220519 MGI 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0013482 abnormal duodenum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20180215 MGI PMID:28137860 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0013956 decreased colon length IAGP N RGD:5509061 20180215 MGI PMID:28137860 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0030633 decreased urine creatine level IAGP N RGD:5509061 20180927 MGI PMID:23026748 731937 Gatm glycine amidinotransferase (L-arginine:glycine amidinotransferase) gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:23026748 731939 Dlg2 discs large MAGUK scaffold protein 2 gene MP:0001035 abnormal submandibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:14724236 731939 Dlg2 discs large MAGUK scaffold protein 2 gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:12890763 731939 Dlg2 discs large MAGUK scaffold protein 2 gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:12890763 731939 Dlg2 discs large MAGUK scaffold protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20230601 MGI PMID:30093633 731939 Dlg2 discs large MAGUK scaffold protein 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12890763 731939 Dlg2 discs large MAGUK scaffold protein 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12890763 731939 Dlg2 discs large MAGUK scaffold protein 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:12890763 731939 Dlg2 discs large MAGUK scaffold protein 2 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:11312293 731939 Dlg2 discs large MAGUK scaffold protein 2 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:12890763 731939 Dlg2 discs large MAGUK scaffold protein 2 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20230601 MGI PMID:30093633 731939 Dlg2 discs large MAGUK scaffold protein 2 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:30093633 731939 Dlg2 discs large MAGUK scaffold protein 2 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20230601 MGI PMID:30093633 731944 Gtf3c1 general transcription factor III C 1 gene MP:0006204 embryonic lethality before implantation IEA N RGD:5509061 20111116 MGI 731944 Gtf3c1 general transcription factor III C 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20240523 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:8081012 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:2723742 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:4118891 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:8081012 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:6123371 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:6127146 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:8081012 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9520333 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000854 abnormal cerebellum development IEA N RGD:5509061 20111116 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:2723742 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9520333 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:11596045 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:4118891 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:9023358 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:9520333 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11596045 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:4118891 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000879 increased Purkinje cell number IEA N RGD:5509061 20111116 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:2077109 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000884 delaminated Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:11596045 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:11596045 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:2723742 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:4118891 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9520333 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:2723742 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:9520333 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:8081012 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:8081012 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:9520333 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:7760215 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11596045 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210128 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001386 abnormal maternal nurturing IEA N RGD:5509061 20111116 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:9023358 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11596045 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:8081012 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9520333 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20201022 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20111116 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:8081012 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10766925 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001922 reduced male fertility IEA N RGD:5509061 20111116 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001923 reduced female fertility IEA N RGD:5509061 20111116 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8081012 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9023358 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:12040038 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20111116 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12040038 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002204 abnormal synaptic neurotransmitter level IAGP N RGD:5509061 20141003 MGI PMID:6127146 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:8855331 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:7760215 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:8081012 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20180405 MGI PMID:29180115 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20180405 MGI PMID:29180115 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:8081012 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:7760215 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:7760215 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:7760215 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:8574680 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7760215 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:9023358 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:2723742 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:7062116 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:7062116 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12040038 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:9023358 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11596045 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:4118891 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:3882972 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8855331 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:8081012 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0004494 abnormal synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:6127146 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:8081012 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:7062116 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:2723742 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9520333 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:11596045 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0006098 absent cerebellar lobules IEA N RGD:5509061 20111116 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:9023358 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7760215 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:10766925 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:7760215 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:8574680 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:11596045 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20230601 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0008911 induced hyperactivity IEA N RGD:5509061 20111116 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0008913 weaving IEA N RGD:5509061 20111116 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0009268 absent cerebellum fissure IEA N RGD:5509061 20111116 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:9023358 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0010011 ectopic hippocampus pyramidal cells IAGP N RGD:5509061 20141003 MGI PMID:8574680 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0010323 retropulsion IAGP N RGD:5509061 20141003 MGI PMID:8081012 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0011084 lethality at weaning, incomplete penetrance IEA N RGD:5509061 20111116 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:7062116 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7760215 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0011940 decreased food intake IEA N RGD:5509061 20141003 MGI 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0012490 abnormal cochlear VIII nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:2077109 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:6123371 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20141003 MGI PMID:7062116 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20141003 MGI PMID:9023358 731945 Kcnj6 potassium inwardly-rectifying channel, subfamily J, member 6 gene MP:0030636 decreased taurine level IAGP N RGD:5509061 20180913 MGI PMID:6127146 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11756685 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21426320 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:21426320 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:15713628 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0000747 muscle weakness IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:10866668 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0000825 dilated lateral ventricle IEA N RGD:5509061 20141003 MGI 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:10866668 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:16751185 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:15713628 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:11514592 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10866668 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:19675577 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10866668 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:12056592 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15001574 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:11756685 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:16581799 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16581799 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16581799 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15033975 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:15033975 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10866668 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0002086 abnormal extraembryonic tissue morphology IEA N RGD:5509061 20111116 MGI 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10866668 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11756685 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16751185 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:11514592 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15033975 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15048110 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:11756685 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:15713628 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16751185 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11756685 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16581799 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0003998 decreased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0004126 thin hypodermis IAGP N RGD:5509061 20141003 MGI PMID:15713628 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:10866668 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15033975 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15048110 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:10866668 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15001574 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21426320 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15001574 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:10866668 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:10866668 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:11756685 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:15033975 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:15048110 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11756685 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11756685 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0009287 decreased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11756685 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11756685 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11756685 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15001574 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15713628 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11514592 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15713628 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0009596 abnormal stratum corneum lipid matrix formation IAGP N RGD:5509061 20141003 MGI PMID:19675577 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15001574 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15001574 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15033975 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0010963 abnormal compact bone volume IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11514592 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11756685 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16581799 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20141003 MGI PMID:11756685 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0012735 abnormal response to exercise IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0013383 increased sebaceous gland adenoma incidence IAGP N RGD:5509061 20141218 MGI PMID:15033975 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0013639 decreased bone stiffness IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0013646 decreased energy dissipated prior to femur fracture IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20151126 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0030009 increased bone marrow adipose tissue amount IAGP N RGD:5509061 20170706 MGI PMID:25279796 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0030576 abnormal keratinocyte adhesion IAGP N RGD:5509061 20180607 MGI PMID:11514592 731946 Ppard peroxisome proliferator activator receptor delta gene MP:0030583 abnormal hair follicle peg morphology IAGP N RGD:5509061 20180614 MGI PMID:15713628 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10769386 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23580201 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11124980 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20201022 MGI 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:23580201 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11124980 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:11124980 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0002188 small heart IEA N RGD:5509061 20181227 MGI 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:10769386 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:23580201 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:23580201 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:11124980 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:23580201 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:14980210 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:10769386 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:11124980 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:23580201 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20170105 MGI 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:10769386 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0005662 increased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:23580201 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0005665 increased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:23580201 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11124980 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10769386 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0009747 impaired behavioral response to xenobiotic IEA N RGD:5509061 20141204 MGI 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:10769386 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:10769386 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0009758 impaired behavioral response to cocaine IEA N RGD:5509061 20141204 MGI 731948 Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 731951 Nrtn neurturin gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10069332 731951 Nrtn neurturin gene MP:0001037 abnormal parasympathetic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10069332 731951 Nrtn neurturin gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:12668632 731951 Nrtn neurturin gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10069332 731951 Nrtn neurturin gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12668632 731951 Nrtn neurturin gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15019945 731951 Nrtn neurturin gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:14507865 731951 Nrtn neurturin gene MP:0001337 dry eyes IAGP N RGD:5509061 20141003 MGI PMID:14507865 731951 Nrtn neurturin gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:10069332 731951 Nrtn neurturin gene MP:0001348 abnormal lacrimal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:10069332 731951 Nrtn neurturin gene MP:0001993 abnormal blinking IAGP N RGD:5509061 20141003 MGI PMID:14507865 731951 Nrtn neurturin gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:10069332 731951 Nrtn neurturin gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:12668632 731951 Nrtn neurturin gene MP:0004990 abnormal ciliary ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10069332 731951 Nrtn neurturin gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:14507865 731951 Nrtn neurturin gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:12668632 731951 Nrtn neurturin gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14507865 731951 Nrtn neurturin gene MP:0006162 thick eyelids IAGP N RGD:5509061 20150212 MGI PMID:10069332 731951 Nrtn neurturin gene MP:0006198 enophthalmos IAGP N RGD:5509061 20150212 MGI PMID:10069332 731951 Nrtn neurturin gene MP:0008313 abnormal parasympathetic postganglionic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10069332 731951 Nrtn neurturin gene MP:0008313 abnormal parasympathetic postganglionic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15019945 731951 Nrtn neurturin gene MP:0008315 abnormal otic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10069332 731951 Nrtn neurturin gene MP:0012164 abnormal conjunctiva goblet cell morphology IAGP N RGD:5509061 20141211 MGI PMID:14507865 731951 Nrtn neurturin gene MP:0013466 keratoconjunctivitis sicca IAGP N RGD:5509061 20150212 MGI PMID:14507865 731951 Nrtn neurturin gene MP:0014149 abnormal lacrimal gland innervation pattern IAGP N RGD:5509061 20160407 MGI PMID:10069332 731951 Nrtn neurturin gene MP:0020220 decreased tear production IAGP N RGD:5509061 20141211 MGI PMID:14507865 731951 Nrtn neurturin gene MP:0020854 increased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:14507865 731953 Ppp1r14d protein phosphatase 1, regulatory inhibitor subunit 14D gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20211021 MGI 731953 Ppp1r14d protein phosphatase 1, regulatory inhibitor subunit 14D gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 731954 Slc36a1 solute carrier family 36 (proton/amino acid symporter), member 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210128 MGI 731954 Slc36a1 solute carrier family 36 (proton/amino acid symporter), member 1 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210128 MGI 731954 Slc36a1 solute carrier family 36 (proton/amino acid symporter), member 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 731954 Slc36a1 solute carrier family 36 (proton/amino acid symporter), member 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210128 MGI 731954 Slc36a1 solute carrier family 36 (proton/amino acid symporter), member 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 731954 Slc36a1 solute carrier family 36 (proton/amino acid symporter), member 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 731954 Slc36a1 solute carrier family 36 (proton/amino acid symporter), member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 731954 Slc36a1 solute carrier family 36 (proton/amino acid symporter), member 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210128 MGI 731956 Tcf12 transcription factor 12 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17442955 731956 Tcf12 transcription factor 12 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8649400 731956 Tcf12 transcription factor 12 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17442955 731956 Tcf12 transcription factor 12 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18384878 731956 Tcf12 transcription factor 12 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11937548 731956 Tcf12 transcription factor 12 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18093538 731956 Tcf12 transcription factor 12 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0004939 abnormal B cell morphology IEA N RGD:5509061 20190404 MGI 731956 Tcf12 transcription factor 12 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18093538 731956 Tcf12 transcription factor 12 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20190404 MGI 731956 Tcf12 transcription factor 12 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442955 731956 Tcf12 transcription factor 12 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:11937548 731956 Tcf12 transcription factor 12 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442955 731956 Tcf12 transcription factor 12 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:18384878 731956 Tcf12 transcription factor 12 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442955 731956 Tcf12 transcription factor 12 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18384878 731956 Tcf12 transcription factor 12 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17442955 731956 Tcf12 transcription factor 12 gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0008037 abnormal T cell morphology IEA N RGD:5509061 20190404 MGI 731956 Tcf12 transcription factor 12 gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18093538 731956 Tcf12 transcription factor 12 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442955 731956 Tcf12 transcription factor 12 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18093538 731956 Tcf12 transcription factor 12 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18384878 731956 Tcf12 transcription factor 12 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11937548 731956 Tcf12 transcription factor 12 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:8649400 731956 Tcf12 transcription factor 12 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190110 MGI 731956 Tcf12 transcription factor 12 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8649400 731956 Tcf12 transcription factor 12 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10958665 731956 Tcf12 transcription factor 12 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8649400 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16964410 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20111116 MGI 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:16964410 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0000160 kyphosis IEA N RGD:5509061 20151015 MGI 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:16964410 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16964410 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:7954802 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:7969468 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0000746 weakness IEA N RGD:5509061 20111116 MGI 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:12704387 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:8618055 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20111116 MGI 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16964410 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001386 abnormal maternal nurturing IEA N RGD:5509061 20111116 MGI 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16964410 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:7954802 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:7969468 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20170706 MGI PMID:26427409 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20111116 MGI 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17270300 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:7969468 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:7969468 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:7954802 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12559117 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:7954802 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:7969468 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:7969468 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001505 hunched posture IEA N RGD:5509061 20111116 MGI 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20111116 MGI 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:17270300 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:7969468 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001524 impaired limb coordination IEA N RGD:5509061 20111116 MGI 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001525 impaired balance IEA N RGD:5509061 20111116 MGI 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:7954802 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:16964410 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16964410 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0002161 abnormal fertility/fecundity IEA N RGD:5509061 20111116 MGI 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15305863 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0002566 abnormal sexual interaction IEA N RGD:5509061 20111116 MGI 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:21356376 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:11739579 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21356376 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17270300 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:21356376 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:21356376 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:16964410 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21356376 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:21356376 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20111116 MGI 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12704387 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8618055 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0010741 abnormal melanocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:8618055 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0011274 short excitatory postsynaptic current decay time IAGP N RGD:5509061 20240418 MGI PMID:11739579 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:21356376 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:21356376 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:21356376 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0011856 abnormal glomerular filtration barrier function IAGP N RGD:5509061 20141003 MGI PMID:21356376 731957 Grm1 glutamate receptor, metabotropic 1 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20170706 MGI PMID:26427409 731960 Grpr gastrin releasing peptide receptor gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:9345264 731960 Grpr gastrin releasing peptide receptor gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:21040852 731960 Grpr gastrin releasing peptide receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9501238 731960 Grpr gastrin releasing peptide receptor gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:9345264 731960 Grpr gastrin releasing peptide receptor gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:9501238 731960 Grpr gastrin releasing peptide receptor gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:9345264 731964 Cnn3 calponin 3, acidic gene MP:0000914 exencephaly IAGP N RGD:5509061 20170314 MGI PMID:26046660 731964 Cnn3 calponin 3, acidic gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20170314 MGI PMID:26046660 731964 Cnn3 calponin 3, acidic gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170314 MGI PMID:26046660 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12540600 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15353487 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180215 MGI PMID:24603714 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12540600 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15353487 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:11874481 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12540600 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15353487 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20180215 MGI PMID:24603714 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:12540600 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15353487 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12540600 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15353487 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20180215 MGI PMID:24603714 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15353487 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005439 decreased glycogen level IAGP N RGD:5509061 20180215 MGI PMID:24603714 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12540600 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15353487 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180215 MGI PMID:24603714 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:12540600 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12540600 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12540600 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20180215 MGI PMID:24603714 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0011015 decreased body surface temperature IAGP N RGD:5509061 20180215 MGI PMID:24603714 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180215 MGI PMID:24603714 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20180215 MGI PMID:24603714 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20180215 MGI PMID:24603714 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:12540600 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:16804058 731966 Fabp5 fatty acid binding protein 5, epidermal gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:16804058 731971 Deaf1 DEAF1, transcription factor gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:14966286 731971 Deaf1 DEAF1, transcription factor gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:14966286 731971 Deaf1 DEAF1, transcription factor gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:14966286 731971 Deaf1 DEAF1, transcription factor gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:14966286 731971 Deaf1 DEAF1, transcription factor gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:14966286 731971 Deaf1 DEAF1, transcription factor gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:24726472 731971 Deaf1 DEAF1, transcription factor gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:14966286 731971 Deaf1 DEAF1, transcription factor gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:14966286 731971 Deaf1 DEAF1, transcription factor gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14966286 731971 Deaf1 DEAF1, transcription factor gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20141003 MGI PMID:24726472 731972 Plpp3 phospholipid phosphatase 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20180621 MGI PMID:19123136 731972 Plpp3 phospholipid phosphatase 3 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20180621 MGI PMID:19123136 731972 Plpp3 phospholipid phosphatase 3 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17610274 731972 Plpp3 phospholipid phosphatase 3 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:17610274 731972 Plpp3 phospholipid phosphatase 3 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20180621 MGI PMID:19123136 731972 Plpp3 phospholipid phosphatase 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17610274 731972 Plpp3 phospholipid phosphatase 3 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20180621 MGI PMID:19123136 731972 Plpp3 phospholipid phosphatase 3 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17610274 731972 Plpp3 phospholipid phosphatase 3 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17610274 731972 Plpp3 phospholipid phosphatase 3 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:17610274 731972 Plpp3 phospholipid phosphatase 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17610274 731972 Plpp3 phospholipid phosphatase 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180621 MGI PMID:19123136 731972 Plpp3 phospholipid phosphatase 3 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20180621 MGI PMID:19123136 731972 Plpp3 phospholipid phosphatase 3 gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:17610274 731972 Plpp3 phospholipid phosphatase 3 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 731972 Plpp3 phospholipid phosphatase 3 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 731972 Plpp3 phospholipid phosphatase 3 gene MP:0008533 abnormal anterior visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:17610274 731972 Plpp3 phospholipid phosphatase 3 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20180621 MGI PMID:19123136 731972 Plpp3 phospholipid phosphatase 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17610274 731972 Plpp3 phospholipid phosphatase 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731972 Plpp3 phospholipid phosphatase 3 gene MP:0011256 abnormal neural fold morphology IAGP N RGD:5509061 20141003 MGI PMID:17610274 731972 Plpp3 phospholipid phosphatase 3 gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0012156 rostral-caudal axis duplication IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0012181 increased somite number IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0012274 increased axial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:12925589 731972 Plpp3 phospholipid phosphatase 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 731974 Stambp STAM binding protein gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11713295 731974 Stambp STAM binding protein gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:11713295 731974 Stambp STAM binding protein gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:11713295 731974 Stambp STAM binding protein gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 731974 Stambp STAM binding protein gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:11713295 731974 Stambp STAM binding protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11713295 731974 Stambp STAM binding protein gene MP:0003900 shortened QT interval IEA N RGD:5509061 20230601 MGI 731974 Stambp STAM binding protein gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11713295 731974 Stambp STAM binding protein gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 731976 Kiss1r KISS1 receptor gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:17699664 731976 Kiss1r KISS1 receptor gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:17699664 731976 Kiss1r KISS1 receptor gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 731976 Kiss1r KISS1 receptor gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:17978050 731976 Kiss1r KISS1 receptor gene MP:0001127 small ovary IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0001143 constricted vagina orifice IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:24051579 731976 Kiss1r KISS1 receptor gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17978050 731976 Kiss1r KISS1 receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0001159 absent prostate gland IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0001159 absent prostate gland IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17699664 731976 Kiss1r KISS1 receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 731976 Kiss1r KISS1 receptor gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17699664 731976 Kiss1r KISS1 receptor gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:17699664 731976 Kiss1r KISS1 receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:24051579 731976 Kiss1r KISS1 receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:24051579 731976 Kiss1r KISS1 receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17699664 731976 Kiss1r KISS1 receptor gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21516099 731976 Kiss1r KISS1 receptor gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:17699664 731976 Kiss1r KISS1 receptor gene MP:0002607 decreased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0002637 small uterus IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0002716 small male preputial gland IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:15665093 731976 Kiss1r KISS1 receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:17699664 731976 Kiss1r KISS1 receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:17978050 731976 Kiss1r KISS1 receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0002774 small prostate gland IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15665093 731976 Kiss1r KISS1 receptor gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:24051579 731976 Kiss1r KISS1 receptor gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0002834 decreased heart weight IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0002965 increased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0002989 small kidney IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0003344 mammary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0003363 decreased circulating gonadotropin level IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0003363 decreased circulating gonadotropin level IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0003379 absent sexual maturation IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0003531 abnormal vagina development IAGP N RGD:5509061 20141003 MGI PMID:21516099 731976 Kiss1r KISS1 receptor gene MP:0003558 absent uterus IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0003578 absent ovary IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17699664 731976 Kiss1r KISS1 receptor gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0003642 absent seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0003967 abnormal follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0003967 abnormal follicle stimulating hormone level IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0003969 abnormal luteinizing hormone level IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0004727 absent epididymis IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17699664 731976 Kiss1r KISS1 receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:24051579 731976 Kiss1r KISS1 receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:17699664 731976 Kiss1r KISS1 receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:21516099 731976 Kiss1r KISS1 receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:24051579 731976 Kiss1r KISS1 receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:17699664 731976 Kiss1r KISS1 receptor gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0004962 decreased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:24051579 731976 Kiss1r KISS1 receptor gene MP:0005148 seminal vesicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:24051579 731976 Kiss1r KISS1 receptor gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0005188 small penis IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0005188 small penis IAGP N RGD:5509061 20141003 MGI PMID:17699664 731976 Kiss1r KISS1 receptor gene MP:0005188 small penis IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0005188 small penis IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20141003 MGI PMID:17699664 731976 Kiss1r KISS1 receptor gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 731976 Kiss1r KISS1 receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0006401 absent male preputial gland IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0006401 absent male preputial gland IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0006415 absent testes IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0008297 retention of the adrenal gland x-zone IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0008940 delayed balanopreputial separation IAGP N RGD:5509061 20150917 MGI PMID:24422632 731976 Kiss1r KISS1 receptor gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21516099 731976 Kiss1r KISS1 receptor gene MP:0008983 small vagina IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:14573733 731976 Kiss1r KISS1 receptor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0009226 small uterine cervix IAGP N RGD:5509061 20141003 MGI PMID:14652023 731976 Kiss1r KISS1 receptor gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0009856 failure of ejaculation IAGP N RGD:5509061 20141003 MGI PMID:17699664 731976 Kiss1r KISS1 receptor gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20170511 MGI 731976 Kiss1r KISS1 receptor gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17595229 731976 Kiss1r KISS1 receptor gene MP:0013308 decreased adrenal gland weight IAGP N RGD:5509061 20141120 MGI PMID:22067321 731976 Kiss1r KISS1 receptor gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:22067321 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:10894163 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:10894163 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10894163 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:10894163 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:10894163 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10894163 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0008073 abnormal CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0008077 abnormal CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16043517 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16043517 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0009625 abnormal abdominal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:20724542 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10894163 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:10894163 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20150219 MGI PMID:24557836 731977 Cflar CASP8 and FADD-like apoptosis regulator gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:10894163 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160922 MGI PMID:25497869 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22753645 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20151112 MGI PMID:25053805 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0002083 premature death IAGP N RGD:5509061 20151112 MGI PMID:25053805 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151112 MGI PMID:25053805 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22753645 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:22753645 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20151112 MGI PMID:25053805 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0003496 increased thyroid adenoma incidence IAGP N RGD:5509061 20160922 MGI PMID:25497869 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20160922 MGI PMID:25497869 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22753645 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22753645 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:22753645 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:22753645 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22753645 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22753645 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22753645 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20151112 MGI PMID:25053805 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:22753645 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20151112 MGI PMID:25053805 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22753645 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20151112 MGI PMID:25053805 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20160922 MGI PMID:25497869 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:22753645 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0012436 increased colon tumor incidence IAGP N RGD:5509061 20151112 MGI PMID:25053805 731978 Ccdc80 coiled-coil domain containing 80 gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20160922 MGI PMID:25497869 731980 Erc1 ELKS/RAB6-interacting/CAST family member 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 731980 Erc1 ELKS/RAB6-interacting/CAST family member 1 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:20932476 731980 Erc1 ELKS/RAB6-interacting/CAST family member 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:20932476 731980 Erc1 ELKS/RAB6-interacting/CAST family member 1 gene MP:0011092 embryonic lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 731980 Erc1 ELKS/RAB6-interacting/CAST family member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 731980 Erc1 ELKS/RAB6-interacting/CAST family member 1 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20220811 MGI 731980 Erc1 ELKS/RAB6-interacting/CAST family member 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15194823 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15184377 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201022 MGI 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15184377 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15194823 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001396 unidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:15184377 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15184377 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15194823 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15184377 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15194823 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:15184377 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:15194823 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:15194823 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:16571783 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:15194823 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15184377 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0001994 increased blinking frequency IAGP N RGD:5509061 20141003 MGI PMID:15194823 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:15194823 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15184377 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20201022 MGI 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:15194823 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0002807 abnormal eye blink conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15194823 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15194823 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:15194823 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0003280 urinary incontinence IAGP N RGD:5509061 20141003 MGI PMID:15184377 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20151119 MGI PMID:25267913 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:16571783 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0004037 increased muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:19220851 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15328414 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17074442 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16763026 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17135251 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0004597 increased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20141003 MGI PMID:17074442 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0004628 Deiters cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15328414 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:15328414 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:15328414 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0004746 abnormal cochlear IHC afferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:16763026 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0004925 decreased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20141003 MGI PMID:17135251 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220519 MGI 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20240530 MGI PMID:33346797 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20151119 MGI PMID:25267913 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19220851 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15328414 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0006324 abnormal cochlear nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:16763026 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0006335 abnormal hearing electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16763026 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:15184377 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:19220851 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0011445 abnormal renal protein reabsorption IAGP N RGD:5509061 20240530 MGI PMID:33346797 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0011535 increased urination frequency IAGP N RGD:5509061 20141003 MGI PMID:15184377 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0011535 increased urination frequency IAGP N RGD:5509061 20141003 MGI PMID:19220851 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0011863 abnormal podocyte physiology IAGP N RGD:5509061 20240530 MGI PMID:33346797 731982 Kcnma1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:16763026 731984 Dnajc14 DnaJ heat shock protein family (Hsp40) member C14 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20211021 MGI 731984 Dnajc14 DnaJ heat shock protein family (Hsp40) member C14 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 731984 Dnajc14 DnaJ heat shock protein family (Hsp40) member C14 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 731984 Dnajc14 DnaJ heat shock protein family (Hsp40) member C14 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 731984 Dnajc14 DnaJ heat shock protein family (Hsp40) member C14 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 731984 Dnajc14 DnaJ heat shock protein family (Hsp40) member C14 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20201231 MGI 731986 Gnb5 guanine nucleotide binding protein (G protein), beta 5 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10749990 731986 Gnb5 guanine nucleotide binding protein (G protein), beta 5 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:10749990 731986 Gnb5 guanine nucleotide binding protein (G protein), beta 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12738888 731986 Gnb5 guanine nucleotide binding protein (G protein), beta 5 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10749990 731986 Gnb5 guanine nucleotide binding protein (G protein), beta 5 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10749990 731986 Gnb5 guanine nucleotide binding protein (G protein), beta 5 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10749990 731986 Gnb5 guanine nucleotide binding protein (G protein), beta 5 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:10749990 731986 Gnb5 guanine nucleotide binding protein (G protein), beta 5 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:10749990 731986 Gnb5 guanine nucleotide binding protein (G protein), beta 5 gene MP:0002082 postnatal lethality IEA N RGD:5509061 20111116 MGI 731986 Gnb5 guanine nucleotide binding protein (G protein), beta 5 gene MP:0002880 opisthotonus IAGP N RGD:5509061 20141003 MGI PMID:10749990 731986 Gnb5 guanine nucleotide binding protein (G protein), beta 5 gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:20884879 731986 Gnb5 guanine nucleotide binding protein (G protein), beta 5 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:12738888 731986 Gnb5 guanine nucleotide binding protein (G protein), beta 5 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:10749990 731986 Gnb5 guanine nucleotide binding protein (G protein), beta 5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12738888 731986 Gnb5 guanine nucleotide binding protein (G protein), beta 5 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 731990 Bcl2l10 Bcl2-like 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12215543 731991 Pcyt2 phosphate cytidylyltransferase 2, ethanolamine gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:19666474 731991 Pcyt2 phosphate cytidylyltransferase 2, ethanolamine gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17325045 731991 Pcyt2 phosphate cytidylyltransferase 2, ethanolamine gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19666474 731991 Pcyt2 phosphate cytidylyltransferase 2, ethanolamine gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19666474 731991 Pcyt2 phosphate cytidylyltransferase 2, ethanolamine gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19666474 731991 Pcyt2 phosphate cytidylyltransferase 2, ethanolamine gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19666474 731991 Pcyt2 phosphate cytidylyltransferase 2, ethanolamine gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17325045 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:16155113 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20181227 MGI PMID:30445045 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0001333 absent optic nerve IEA N RGD:5509061 20210128 MGI 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20181227 MGI PMID:30445045 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16597347 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16597347 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16597347 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20181227 MGI PMID:30445045 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20150514 MGI PMID:24466230 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20150514 MGI PMID:24466230 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16155113 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16155113 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16597347 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16155113 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20150514 MGI PMID:24466230 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16155113 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16597347 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16597347 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20181227 MGI PMID:30445045 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20181227 MGI PMID:30445045 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20150514 MGI PMID:24466230 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20150514 MGI PMID:24466230 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20150514 MGI PMID:24466230 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20150514 MGI PMID:24466230 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:16155113 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20181227 MGI PMID:30445045 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0008520 disorganized retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:16597347 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0009392 retina gliosis IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20150514 MGI PMID:24466230 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0010749 absent visual evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16155113 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20141003 MGI PMID:16155113 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20150514 MGI PMID:24466230 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20181227 MGI PMID:30445045 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0012034 abnormal a-wave shape IAGP N RGD:5509061 20150514 MGI PMID:24466230 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0012035 abnormal b-wave shape IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0012035 abnormal b-wave shape IAGP N RGD:5509061 20150514 MGI PMID:24466230 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20150514 MGI PMID:24466230 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20181227 MGI PMID:30445045 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20141003 MGI PMID:24163243 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20150514 MGI PMID:24466230 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20181227 MGI PMID:30445045 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0012671 retina spots IAGP N RGD:5509061 20181227 MGI PMID:30445045 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0020439 absent b-wave IAGP N RGD:5509061 20181227 MGI PMID:30445045 731993 Cacna1f calcium channel, voltage-dependent, alpha 1F subunit gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:24466230 731997 Unc5a unc-5 netrin receptor A gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:16829956 731997 Unc5a unc-5 netrin receptor A gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16829956 731997 Unc5a unc-5 netrin receptor A gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:16829956 732000 Slc17a3 solute carrier family 17 (sodium phosphate), member 3 gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20240808 MGI PMID:38641061 732000 Slc17a3 solute carrier family 17 (sodium phosphate), member 3 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20240808 MGI PMID:38641061 732000 Slc17a3 solute carrier family 17 (sodium phosphate), member 3 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20240808 MGI PMID:38641061 732000 Slc17a3 solute carrier family 17 (sodium phosphate), member 3 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20240808 MGI PMID:38641061 732000 Slc17a3 solute carrier family 17 (sodium phosphate), member 3 gene MP:0011424 decreased urine uric acid level IAGP N RGD:5509061 20240808 MGI PMID:38641061 732000 Slc17a3 solute carrier family 17 (sodium phosphate), member 3 gene MP:0031487 increased circulating hypoxanthine level IAGP N RGD:5509061 20240808 MGI PMID:38641061 732004 Scg3 secretogranin III gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 732004 Scg3 secretogranin III gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20160128 MGI 732004 Scg3 secretogranin III gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220519 MGI 732004 Scg3 secretogranin III gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20180614 MGI PMID:29281094 732004 Scg3 secretogranin III gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180614 MGI PMID:29281094 732004 Scg3 secretogranin III gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180614 MGI PMID:29281094 732004 Scg3 secretogranin III gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20180614 MGI PMID:29281094 732004 Scg3 secretogranin III gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180614 MGI PMID:29281094 732007 Casp6 caspase 6 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22262731 732007 Casp6 caspase 6 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15994297 732007 Casp6 caspase 6 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:15994297 732007 Casp6 caspase 6 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15994297 732007 Casp6 caspase 6 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22262731 732007 Casp6 caspase 6 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:22262731 732007 Casp6 caspase 6 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:22262731 732007 Casp6 caspase 6 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:15994297 732007 Casp6 caspase 6 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:22262731 732007 Casp6 caspase 6 gene MP:0010259 anterior polar cataract IAGP N RGD:5509061 20141003 MGI PMID:15994297 732007 Casp6 caspase 6 gene MP:0012467 increased striatum size IAGP N RGD:5509061 20161222 MGI PMID:22262731 732009 Fut4 fucosyltransferase 4 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11485743 732009 Fut4 fucosyltransferase 4 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11485743 732009 Fut4 fucosyltransferase 4 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11485743 732009 Fut4 fucosyltransferase 4 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:11485743 732009 Fut4 fucosyltransferase 4 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 732009 Fut4 fucosyltransferase 4 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11485743 732009 Fut4 fucosyltransferase 4 gene MP:0002345 abnormal lymph node primary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11485743 732009 Fut4 fucosyltransferase 4 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12869507 732009 Fut4 fucosyltransferase 4 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11485743 732009 Fut4 fucosyltransferase 4 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:11485743 732009 Fut4 fucosyltransferase 4 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:11485743 732009 Fut4 fucosyltransferase 4 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:11485743 732009 Fut4 fucosyltransferase 4 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 732009 Fut4 fucosyltransferase 4 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11485743 732009 Fut4 fucosyltransferase 4 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15308551 732009 Fut4 fucosyltransferase 4 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210128 MGI 732009 Fut4 fucosyltransferase 4 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11535629 732009 Fut4 fucosyltransferase 4 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11485743 732009 Fut4 fucosyltransferase 4 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11535629 732009 Fut4 fucosyltransferase 4 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 732009 Fut4 fucosyltransferase 4 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 732009 Fut4 fucosyltransferase 4 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:11485743 732009 Fut4 fucosyltransferase 4 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20211021 MGI 732012 Agps alkylglycerone phosphate synthase gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21353609 732012 Agps alkylglycerone phosphate synthase gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:16332269 732012 Agps alkylglycerone phosphate synthase gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:21353609 732012 Agps alkylglycerone phosphate synthase gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:21353609 732012 Agps alkylglycerone phosphate synthase gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:16332269 732012 Agps alkylglycerone phosphate synthase gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:21353609 732012 Agps alkylglycerone phosphate synthase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:21353609 732012 Agps alkylglycerone phosphate synthase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16332269 732012 Agps alkylglycerone phosphate synthase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21353609 732012 Agps alkylglycerone phosphate synthase gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21353609 732012 Agps alkylglycerone phosphate synthase gene MP:0002579 disorganized secondary lens fibers IAGP N RGD:5509061 20141003 MGI PMID:21353609 732012 Agps alkylglycerone phosphate synthase gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21353609 732012 Agps alkylglycerone phosphate synthase gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:21353609 732012 Agps alkylglycerone phosphate synthase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21353609 732015 Rln1 relaxin 1 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9886856 732015 Rln1 relaxin 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9886856 732015 Rln1 relaxin 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0002774 small prostate gland IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0004514 dystocia IAGP N RGD:5509061 20141003 MGI PMID:9886856 732015 Rln1 relaxin 1 gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0006078 abnormal nipple morphology IAGP N RGD:5509061 20141003 MGI PMID:9886856 732015 Rln1 relaxin 1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:9886856 732015 Rln1 relaxin 1 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:9886856 732015 Rln1 relaxin 1 gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:9886856 732015 Rln1 relaxin 1 gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:9886856 732015 Rln1 relaxin 1 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:9886856 732015 Rln1 relaxin 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:9886856 732015 Rln1 relaxin 1 gene MP:0009575 abnormal pubic symphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9886856 732015 Rln1 relaxin 1 gene MP:0009735 abnormal prostate gland development IAGP N RGD:5509061 20141003 MGI PMID:12861045 732015 Rln1 relaxin 1 gene MP:0013713 decreased nipple size IAGP N RGD:5509061 20150402 MGI PMID:9886856 732017 Tff1 trefoil factor 1 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:8824193 732017 Tff1 trefoil factor 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:8824193 732017 Tff1 trefoil factor 1 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:8824193 732017 Tff1 trefoil factor 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 732017 Tff1 trefoil factor 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8824193 732017 Tff1 trefoil factor 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 732017 Tff1 trefoil factor 1 gene MP:0005211 increased stomach mucosa thickness IAGP N RGD:5509061 20141003 MGI PMID:12768581 732017 Tff1 trefoil factor 1 gene MP:0005211 increased stomach mucosa thickness IAGP N RGD:5509061 20141003 MGI PMID:8824193 732017 Tff1 trefoil factor 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20141003 MGI 732017 Tff1 trefoil factor 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 732017 Tff1 trefoil factor 1 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20141003 MGI 732017 Tff1 trefoil factor 1 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12768581 732017 Tff1 trefoil factor 1 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8824193 732017 Tff1 trefoil factor 1 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:12768581 732018 Gpr156 G protein-coupled receptor 156 gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 732018 Gpr156 G protein-coupled receptor 156 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201231 MGI 732026 Dync1i2 dynein cytoplasmic 1 intermediate chain 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20141003 MGI 732026 Dync1i2 dynein cytoplasmic 1 intermediate chain 2 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 732026 Dync1i2 dynein cytoplasmic 1 intermediate chain 2 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20160804 MGI 732026 Dync1i2 dynein cytoplasmic 1 intermediate chain 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:10640277 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:11825874 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8221886 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0001034 abnormal parasympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8221886 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8221886 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0001048 absent enteric neurons IAGP N RGD:5509061 20141003 MGI PMID:8221886 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:9126746 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:8221886 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8221886 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21483754 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16690754 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11825874 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0003861 abnormal nervous system development IEA N RGD:5509061 20111215 MGI 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:19208224 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19208224 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10882479 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:19208224 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:19208224 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:18448566 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11032813 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:21435554 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19208224 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8221886 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0006096 absent retina bipolar cells IAGP N RGD:5509061 20141003 MGI PMID:11032813 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20141003 MGI PMID:11032813 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0006105 small tectum IAGP N RGD:5509061 20141003 MGI PMID:11032813 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8221886 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:8221886 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:11032813 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0010916 decreased solitary pulmonary neuroendocrine cell number IAGP N RGD:5509061 20141003 MGI PMID:10952889 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0010917 absent solitary pulmonary neuroendocrine cells IAGP N RGD:5509061 20141003 MGI PMID:10952889 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0010917 absent solitary pulmonary neuroendocrine cells IAGP N RGD:5509061 20141003 MGI PMID:9126746 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0010920 decreased number of pulmonary neuroendocrine bodies IAGP N RGD:5509061 20141003 MGI PMID:10952889 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0010921 absent pulmonary neuroendocrine bodies IAGP N RGD:5509061 20141003 MGI PMID:10952889 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0010921 absent pulmonary neuroendocrine bodies IAGP N RGD:5509061 20141003 MGI PMID:9126746 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11825874 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8221886 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15105417 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11032813 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:24179156 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0012069 abnormal horizontal basal cell of olfactory epithelium morphology IAGP N RGD:5509061 20160407 MGI PMID:21677159 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20161117 MGI PMID:24179156 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0021091 abnormal dorsal interneuron morphology IAGP N RGD:5509061 20220310 MGI PMID:15901662 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0021093 abnormal dorsal interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:15901662 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0021094 abnormal dorsal interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:15901662 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0021095 abnormal dorsal interneuron 4 morphology IAGP N RGD:5509061 20220310 MGI PMID:15901662 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0021096 abnormal dorsal interneuron 5 morphology IAGP N RGD:5509061 20220310 MGI PMID:15901662 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0021097 abnormal dorsal interneuron 6 morphology IAGP N RGD:5509061 20220310 MGI PMID:15901662 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0021099 abnormal dorsal interneuron LA morphology IAGP N RGD:5509061 20220310 MGI PMID:16690754 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:11825874 732027 Ascl1 achaete-scute family bHLH transcription factor 1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:15105417 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:23794065 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17374637 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20170629 MGI PMID:27229122 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20170629 MGI PMID:27229122 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20220407 MGI PMID:17374637 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:14745002 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17374637 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23794065 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14745002 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17374637 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17374637 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0002580 duodenal lesions IAGP N RGD:5509061 20170629 MGI PMID:27229122 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20170629 MGI PMID:27229122 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0002783 abnormal ovary secretion IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23794065 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:14745002 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20170629 MGI PMID:27229122 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20170629 MGI PMID:27229122 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:14745002 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0003696 abnormal zona pellucida morphology IAGP N RGD:5509061 20141003 MGI PMID:17374637 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0003696 abnormal zona pellucida morphology IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:23794065 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:17374637 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:23794065 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14745002 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14745002 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20170629 MGI PMID:27229122 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0009311 increased duodenum adenocarcinoma incidence IAGP N RGD:5509061 20170629 MGI PMID:27229122 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0009375 thin zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:17374637 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23794065 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14745002 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0011124 increased primary ovarian follicle number IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20170119 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20141003 MGI PMID:17062753 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0012408 increased duodenum glandular epithelium tumor incidence IAGP N RGD:5509061 20170629 MGI PMID:27229122 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0013482 abnormal duodenum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20170629 MGI PMID:27229122 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0020326 dilated capillary IAGP N RGD:5509061 20160714 MGI PMID:14745002 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0030025 giant platelets IAGP N RGD:5509061 20170803 MGI PMID:23794065 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20200130 MGI PMID:21239444 732030 C1galt1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:21239444 732032 Mvk mevalonate kinase gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 732032 Mvk mevalonate kinase gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20181227 MGI 732032 Mvk mevalonate kinase gene MP:0001297 microphthalmia IEA N RGD:5509061 20181227 MGI 732032 Mvk mevalonate kinase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 732032 Mvk mevalonate kinase gene MP:0004930 small epididymis IEA N RGD:5509061 20181227 MGI 732032 Mvk mevalonate kinase gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 732032 Mvk mevalonate kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 732032 Mvk mevalonate kinase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 732032 Mvk mevalonate kinase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 732034 Clstn3 calsyntenin 3 gene MP:0000745 tremors IEA N RGD:5509061 20160421 MGI 732034 Clstn3 calsyntenin 3 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:24094106 732034 Clstn3 calsyntenin 3 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20201022 MGI 732034 Clstn3 calsyntenin 3 gene MP:0001406 abnormal gait IEA N RGD:5509061 20170105 MGI 732034 Clstn3 calsyntenin 3 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20200924 MGI PMID:32382066 732034 Clstn3 calsyntenin 3 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20200924 MGI PMID:32382066 732034 Clstn3 calsyntenin 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200924 MGI PMID:32382066 732034 Clstn3 calsyntenin 3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:24094106 732034 Clstn3 calsyntenin 3 gene MP:0003109 short femur IAGP N RGD:5509061 20200924 MGI PMID:32382066 732034 Clstn3 calsyntenin 3 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 732034 Clstn3 calsyntenin 3 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20200924 MGI PMID:32382066 732034 Clstn3 calsyntenin 3 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220519 MGI 732034 Clstn3 calsyntenin 3 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20200924 MGI PMID:32382066 732034 Clstn3 calsyntenin 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200924 MGI PMID:32382066 732034 Clstn3 calsyntenin 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200924 MGI PMID:32382066 732034 Clstn3 calsyntenin 3 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20200924 MGI PMID:32382066 732034 Clstn3 calsyntenin 3 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:24094106 732034 Clstn3 calsyntenin 3 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:24094106 732034 Clstn3 calsyntenin 3 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20200924 MGI PMID:32382066 732034 Clstn3 calsyntenin 3 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20200924 MGI PMID:32382066 732034 Clstn3 calsyntenin 3 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20200924 MGI PMID:32382066 732034 Clstn3 calsyntenin 3 gene MP:0010962 decreased compact bone mass IAGP N RGD:5509061 20200924 MGI PMID:32382066 732034 Clstn3 calsyntenin 3 gene MP:0011151 abnormal hippocampus stratum radiatum morphology IAGP N RGD:5509061 20141003 MGI PMID:24094106 732034 Clstn3 calsyntenin 3 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:24094106 732034 Clstn3 calsyntenin 3 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:24094106 732034 Clstn3 calsyntenin 3 gene MP:0014440 increased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:32382066 732034 Clstn3 calsyntenin 3 gene MP:0031008 decreased bone marrow adipose tissue amount IAGP N RGD:5509061 20200924 MGI PMID:32382066 732037 Surf1 surfeit gene 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:12566387 732037 Surf1 surfeit gene 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12566387 732037 Surf1 surfeit gene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12566387 732037 Surf1 surfeit gene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12566387 732037 Surf1 surfeit gene 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12566387 732037 Surf1 surfeit gene 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17210671 732037 Surf1 surfeit gene 1 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:17210671 732037 Surf1 surfeit gene 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12566387 732037 Surf1 surfeit gene 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:12566387 732037 Surf1 surfeit gene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12566387 732037 Surf1 surfeit gene 1 gene MP:0004198 abnormal fetal size IAGP N RGD:5509061 20141003 MGI PMID:17210671 732037 Surf1 surfeit gene 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17210671 732037 Surf1 surfeit gene 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:17210671 732037 Surf1 surfeit gene 1 gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20141003 MGI PMID:21723506 732037 Surf1 surfeit gene 1 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17210671 732037 Surf1 surfeit gene 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:12566387 732037 Surf1 surfeit gene 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:12566387 732037 Surf1 surfeit gene 1 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:21723506 732037 Surf1 surfeit gene 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12566387 732037 Surf1 surfeit gene 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17210671 732037 Surf1 surfeit gene 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12566387 732041 Syngr2 synaptogyrin 2 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 732041 Syngr2 synaptogyrin 2 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20240523 MGI 732041 Syngr2 synaptogyrin 2 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20240523 MGI 732041 Syngr2 synaptogyrin 2 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 732041 Syngr2 synaptogyrin 2 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18509043 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20190228 MGI PMID:19515912 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20190228 MGI PMID:20981830 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0001147 small testis IAGP N RGD:5509061 20190228 MGI PMID:20981830 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20141003 MGI 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190228 MGI PMID:19515912 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20190228 MGI PMID:20981830 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20190228 MGI PMID:19515912 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20190228 MGI PMID:20981830 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20190228 MGI PMID:19515912 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0002763 ectopic Bergmann glia cells IAGP N RGD:5509061 20190228 MGI PMID:19515912 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20190228 MGI PMID:20981830 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18509043 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0003998 decreased thermal nociceptive threshold IEA N RGD:5509061 20141003 MGI 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20190228 MGI PMID:19515912 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20190228 MGI PMID:19515912 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20190228 MGI PMID:20981830 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:18509043 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0006419 disorganized testis cords IAGP N RGD:5509061 20190228 MGI PMID:20981830 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0008030 abnormal Cajal-Retzius cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18509043 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0009964 abnormal cerebellum lobule morphology IAGP N RGD:5509061 20190228 MGI PMID:19515912 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20190228 MGI PMID:19515912 732043 Adgrg1 adhesion G protein-coupled receptor G1 gene MP:0020560 abnormal pontine nuclei morphology IAGP N RGD:5509061 20190228 MGI PMID:19515912 732044 Cdhr5 cadherin-related family member 5 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20210617 MGI PMID:33188295 732044 Cdhr5 cadherin-related family member 5 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20210617 MGI PMID:33188295 732044 Cdhr5 cadherin-related family member 5 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20210617 MGI PMID:33188295 732045 Cysltr2 cysteinyl leukotriene receptor 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 732045 Cysltr2 cysteinyl leukotriene receptor 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 732045 Cysltr2 cysteinyl leukotriene receptor 2 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:18276782 732045 Cysltr2 cysteinyl leukotriene receptor 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 732045 Cysltr2 cysteinyl leukotriene receptor 2 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 732045 Cysltr2 cysteinyl leukotriene receptor 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:23504326 732045 Cysltr2 cysteinyl leukotriene receptor 2 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:22416124 732045 Cysltr2 cysteinyl leukotriene receptor 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 732045 Cysltr2 cysteinyl leukotriene receptor 2 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20220811 MGI 732045 Cysltr2 cysteinyl leukotriene receptor 2 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 732045 Cysltr2 cysteinyl leukotriene receptor 2 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:22416124 732045 Cysltr2 cysteinyl leukotriene receptor 2 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:15328359 732045 Cysltr2 cysteinyl leukotriene receptor 2 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15328359 732045 Cysltr2 cysteinyl leukotriene receptor 2 gene MP:0009811 abnormal prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:15328359 732047 Opn1sw opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan) gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22674284 732047 Opn1sw opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan) gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:22674284 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0001304 cataract IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17439947 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20160804 MGI 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160922 MGI PMID:24652767 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20190124 MGI PMID:25340873 732049 Prmt3 protein arginine N-methyltransferase 3 gene MP:0011156 abnormal hypodermis fat layer morphology IAGP N RGD:5509061 20190124 MGI PMID:25340873 732050 Fgf5 fibroblast growth factor 5 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20111116 MGI 732050 Fgf5 fibroblast growth factor 5 gene MP:0000397 abnormal guard hair morphology IEA N RGD:5509061 20111116 MGI 732050 Fgf5 fibroblast growth factor 5 gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20141003 MGI PMID:6397398 732050 Fgf5 fibroblast growth factor 5 gene MP:0000405 abnormal auchene hair morphology IAGP N RGD:5509061 20141003 MGI PMID:6397398 732050 Fgf5 fibroblast growth factor 5 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:6397398 732050 Fgf5 fibroblast growth factor 5 gene MP:0001281 increased vibrissae length IEA N RGD:5509061 20111116 MGI 732050 Fgf5 fibroblast growth factor 5 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:6397398 732050 Fgf5 fibroblast growth factor 5 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:7923352 732050 Fgf5 fibroblast growth factor 5 gene MP:0002881 long hair IAGP N RGD:5509061 20141003 MGI PMID:12917328 732050 Fgf5 fibroblast growth factor 5 gene MP:0002881 long hair IAGP N RGD:5509061 20141003 MGI PMID:7923352 732050 Fgf5 fibroblast growth factor 5 gene MP:0008858 abnormal hair cycle anagen phase IEA N RGD:5509061 20111116 MGI 732050 Fgf5 fibroblast growth factor 5 gene MP:0009271 increased guard hair length IAGP N RGD:5509061 20141003 MGI PMID:6397398 732052 Efna5 ephrin A5 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:11089974 732052 Efna5 ephrin A5 gene MP:0000642 enlarged adrenal glands IEA N RGD:5509061 20220519 MGI 732052 Efna5 ephrin A5 gene MP:0000771 abnormal brain size IAGP N RGD:5509061 20141003 MGI PMID:11089974 732052 Efna5 ephrin A5 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:16025107 732052 Efna5 ephrin A5 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:11089974 732052 Efna5 ephrin A5 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:10774725 732052 Efna5 ephrin A5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220512 MGI PMID:26672804 732052 Efna5 ephrin A5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12914696 732052 Efna5 ephrin A5 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 732052 Efna5 ephrin A5 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 732052 Efna5 ephrin A5 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20240523 MGI 732052 Efna5 ephrin A5 gene MP:0001314 cornea opacity IEA N RGD:5509061 20240523 MGI 732052 Efna5 ephrin A5 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20240523 MGI 732052 Efna5 ephrin A5 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20210128 MGI 732052 Efna5 ephrin A5 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:12914696 732052 Efna5 ephrin A5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20200402 MGI 732052 Efna5 ephrin A5 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20201022 MGI 732052 Efna5 ephrin A5 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:11089974 732052 Efna5 ephrin A5 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220512 MGI PMID:26672804 732052 Efna5 ephrin A5 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 732052 Efna5 ephrin A5 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220512 MGI PMID:26672804 732052 Efna5 ephrin A5 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11089974 732052 Efna5 ephrin A5 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20220512 MGI PMID:26672804 732052 Efna5 ephrin A5 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:12914696 732052 Efna5 ephrin A5 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20201022 MGI 732052 Efna5 ephrin A5 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20220519 MGI 732052 Efna5 ephrin A5 gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20220512 MGI PMID:26672804 732052 Efna5 ephrin A5 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:11089974 732052 Efna5 ephrin A5 gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20220512 MGI PMID:26672804 732052 Efna5 ephrin A5 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20220519 MGI 732052 Efna5 ephrin A5 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160421 MGI 732052 Efna5 ephrin A5 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12417660 732052 Efna5 ephrin A5 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20220519 MGI 732052 Efna5 ephrin A5 gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20220512 MGI PMID:26672804 732052 Efna5 ephrin A5 gene MP:0009648 abnormal superovulation IAGP N RGD:5509061 20220512 MGI PMID:26672804 732052 Efna5 ephrin A5 gene MP:0009709 hydrometra IEA N RGD:5509061 20220519 MGI 732052 Efna5 ephrin A5 gene MP:0009945 abnormal accessory olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:11222144 732052 Efna5 ephrin A5 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 732052 Efna5 ephrin A5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12914696 732052 Efna5 ephrin A5 gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20141003 MGI PMID:11089974 732052 Efna5 ephrin A5 gene MP:0011700 increased cumulus expansion IAGP N RGD:5509061 20220512 MGI PMID:26672804 732052 Efna5 ephrin A5 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 732052 Efna5 ephrin A5 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:26672804 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0000199 abnormal circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:18296417 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:18296417 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18296417 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20141003 MGI PMID:18296417 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18296417 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:18296417 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:18296417 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0005568 increased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:18296417 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0005633 increased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:18296417 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0006357 abnormal circulating mineral level IAGP N RGD:5509061 20141003 MGI PMID:18296417 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0008805 decreased circulating amylase level IAGP N RGD:5509061 20141003 MGI PMID:18296417 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18296417 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:18296417 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18296417 732053 Slco1b2 solute carrier organic anion transporter family, member 1b2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 732055 P2ry6 pyrimidinergic receptor P2Y, G-protein coupled, 6 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21724990 732055 P2ry6 pyrimidinergic receptor P2Y, G-protein coupled, 6 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:21724990 732055 P2ry6 pyrimidinergic receptor P2Y, G-protein coupled, 6 gene MP:0002281 abnormal respiratory mucosa goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21724990 732055 P2ry6 pyrimidinergic receptor P2Y, G-protein coupled, 6 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18523137 732055 P2ry6 pyrimidinergic receptor P2Y, G-protein coupled, 6 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:21724990 732055 P2ry6 pyrimidinergic receptor P2Y, G-protein coupled, 6 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:18523137 732055 P2ry6 pyrimidinergic receptor P2Y, G-protein coupled, 6 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:21724990 732055 P2ry6 pyrimidinergic receptor P2Y, G-protein coupled, 6 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21724990 732055 P2ry6 pyrimidinergic receptor P2Y, G-protein coupled, 6 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:18523137 732055 P2ry6 pyrimidinergic receptor P2Y, G-protein coupled, 6 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21724990 732055 P2ry6 pyrimidinergic receptor P2Y, G-protein coupled, 6 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:21724990 732055 P2ry6 pyrimidinergic receptor P2Y, G-protein coupled, 6 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:21724990 732055 P2ry6 pyrimidinergic receptor P2Y, G-protein coupled, 6 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:21724990 732055 P2ry6 pyrimidinergic receptor P2Y, G-protein coupled, 6 gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:21724990 732057 Trip10 thyroid hormone receptor interactor 10 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:20805498 732057 Trip10 thyroid hormone receptor interactor 10 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:20805498 732057 Trip10 thyroid hormone receptor interactor 10 gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20805498 732057 Trip10 thyroid hormone receptor interactor 10 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20805498 732057 Trip10 thyroid hormone receptor interactor 10 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:20805498 732057 Trip10 thyroid hormone receptor interactor 10 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19920150 732057 Trip10 thyroid hormone receptor interactor 10 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:20805498 732057 Trip10 thyroid hormone receptor interactor 10 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20805498 732057 Trip10 thyroid hormone receptor interactor 10 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:20805498 732057 Trip10 thyroid hormone receptor interactor 10 gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:20805498 732057 Trip10 thyroid hormone receptor interactor 10 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:19920150 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20160915 MGI PMID:24697507 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20151231 MGI PMID:24569712 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20151231 MGI PMID:24569712 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0002083 premature death IAGP N RGD:5509061 20151231 MGI PMID:24569712 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:22819676 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20160915 MGI PMID:24697507 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20151231 MGI PMID:24569712 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20160915 MGI PMID:24697507 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:22819676 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:22819676 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:22819676 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20160915 MGI PMID:24697507 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20151231 MGI PMID:24569712 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20160915 MGI PMID:24697507 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20151231 MGI PMID:24569712 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20151231 MGI PMID:24569712 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20160915 MGI PMID:24697507 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20151231 MGI PMID:24569712 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20151231 MGI PMID:24569712 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20151231 MGI PMID:24569712 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20151231 MGI PMID:24569712 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0010761 abnormal microglial cell chemotaxis IAGP N RGD:5509061 20160915 MGI PMID:24697507 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20151231 MGI PMID:24569712 732059 Ndrg2 N-myc downstream regulated gene 2 gene MP:0012066 decreased astrocyte number IAGP N RGD:5509061 20160915 MGI PMID:24697507 732062 Cdk4 cyclin dependent kinase 4 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15315761 732062 Cdk4 cyclin dependent kinase 4 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:17700700 732062 Cdk4 cyclin dependent kinase 4 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19383288 732062 Cdk4 cyclin dependent kinase 4 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17700700 732062 Cdk4 cyclin dependent kinase 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20609353 732062 Cdk4 cyclin dependent kinase 4 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20201231 MGI 732062 Cdk4 cyclin dependent kinase 4 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15315761 732062 Cdk4 cyclin dependent kinase 4 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17700700 732062 Cdk4 cyclin dependent kinase 4 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19383288 732062 Cdk4 cyclin dependent kinase 4 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:19383288 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10490638 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10490638 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:10490638 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:10490638 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:10490638 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001212 skin lesions IAGP N RGD:5509061 20150827 MGI PMID:20718941 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16730350 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19383288 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10490638 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19383288 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20181220 MGI PMID:16877364 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20190124 MGI PMID:28096290 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001627 abnormal cardiac output IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:19383288 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20170105 MGI 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15315761 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17700700 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:10490638 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10490638 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16730350 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10490638 732062 Cdk4 cyclin dependent kinase 4 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16730350 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:12957286 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20609353 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12957286 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12957286 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12957286 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20609353 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002078 abnormal glucose homeostasis IEA N RGD:5509061 20111116 MGI 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19383288 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:10490638 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20160211 MGI 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002340 abnormal axillary lymph node morphology IAGP N RGD:5509061 20181220 MGI PMID:16877364 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002353 abnormal inguinal lymph node morphology IAGP N RGD:5509061 20181220 MGI PMID:16877364 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15315761 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:10490638 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10490638 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002785 absent Leydig cells IAGP N RGD:5509061 20141003 MGI PMID:16730350 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15315761 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19383288 732062 Cdk4 cyclin dependent kinase 4 gene MP:0002893 ketoaciduria IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16730350 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:19383288 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003356 impaired luteinization IAGP N RGD:5509061 20141003 MGI PMID:10490638 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20609353 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20181220 MGI PMID:16877364 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19383288 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12957286 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20181220 MGI PMID:16877364 732062 Cdk4 cyclin dependent kinase 4 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20190124 MGI PMID:28096290 732062 Cdk4 cyclin dependent kinase 4 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20181220 MGI PMID:16877364 732062 Cdk4 cyclin dependent kinase 4 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20190124 MGI PMID:28096290 732062 Cdk4 cyclin dependent kinase 4 gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20150827 MGI PMID:20718941 732062 Cdk4 cyclin dependent kinase 4 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:19383288 732062 Cdk4 cyclin dependent kinase 4 gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:17700700 732062 Cdk4 cyclin dependent kinase 4 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:19383288 732062 Cdk4 cyclin dependent kinase 4 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:16730350 732062 Cdk4 cyclin dependent kinase 4 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:15315761 732062 Cdk4 cyclin dependent kinase 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:16730350 732062 Cdk4 cyclin dependent kinase 4 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:10490638 732062 Cdk4 cyclin dependent kinase 4 gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:19383288 732062 Cdk4 cyclin dependent kinase 4 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17700700 732062 Cdk4 cyclin dependent kinase 4 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20609353 732062 Cdk4 cyclin dependent kinase 4 gene MP:0008332 decreased lactotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:16730350 732062 Cdk4 cyclin dependent kinase 4 gene MP:0008365 adenohypophysis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16730350 732062 Cdk4 cyclin dependent kinase 4 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0009143 abnormal pancreatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:12957286 732062 Cdk4 cyclin dependent kinase 4 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:10319860 732062 Cdk4 cyclin dependent kinase 4 gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20609353 732062 Cdk4 cyclin dependent kinase 4 gene MP:0009623 enlarged inguinal lymph nodes IAGP N RGD:5509061 20181220 MGI PMID:16877364 732062 Cdk4 cyclin dependent kinase 4 gene MP:0009631 enlarged axillary lymph nodes IAGP N RGD:5509061 20181220 MGI PMID:16877364 732062 Cdk4 cyclin dependent kinase 4 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20181220 MGI PMID:16877364 732062 Cdk4 cyclin dependent kinase 4 gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20150827 MGI PMID:20718941 732062 Cdk4 cyclin dependent kinase 4 gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20181220 MGI PMID:16877364 732062 Cdk4 cyclin dependent kinase 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0010741 abnormal melanocyte proliferation IAGP N RGD:5509061 20150827 MGI PMID:20718941 732062 Cdk4 cyclin dependent kinase 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10490638 732062 Cdk4 cyclin dependent kinase 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15315761 732062 Cdk4 cyclin dependent kinase 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19383288 732062 Cdk4 cyclin dependent kinase 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17700700 732062 Cdk4 cyclin dependent kinase 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17700700 732062 Cdk4 cyclin dependent kinase 4 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15315761 732062 Cdk4 cyclin dependent kinase 4 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20170105 MGI 732062 Cdk4 cyclin dependent kinase 4 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:19383288 732062 Cdk4 cyclin dependent kinase 4 gene MP:0012022 increased melanocyte number IAGP N RGD:5509061 20150827 MGI PMID:20718941 732062 Cdk4 cyclin dependent kinase 4 gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:16678773 732062 Cdk4 cyclin dependent kinase 4 gene MP:0031419 delayed estrus IAGP N RGD:5509061 20220630 MGI PMID:10319860 732063 Fabp9 fatty acid binding protein 9, testis gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:20920498 732064 Kcnk2 potassium channel, subfamily K, member 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201231 MGI 732064 Kcnk2 potassium channel, subfamily K, member 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:15175651 732064 Kcnk2 potassium channel, subfamily K, member 2 gene MP:0003075 abnormal response to CNS ischemic injury IAGP N RGD:5509061 20141003 MGI PMID:15175651 732064 Kcnk2 potassium channel, subfamily K, member 2 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:15175651 732064 Kcnk2 potassium channel, subfamily K, member 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15175651 732064 Kcnk2 potassium channel, subfamily K, member 2 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15175651 732064 Kcnk2 potassium channel, subfamily K, member 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15175651 732064 Kcnk2 potassium channel, subfamily K, member 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15175651 732068 Hspbap1 Hspb associated protein 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20200402 MGI 732068 Hspbap1 Hspb associated protein 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 732068 Hspbap1 Hspb associated protein 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200402 MGI 732070 Fap fibroblast activation protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10629066 732070 Fap fibroblast activation protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11330865 732071 Slc25a10 solute carrier family 25 (mitochondrial carrier, dicarboxylate transporter), member 10 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 732071 Slc25a10 solute carrier family 25 (mitochondrial carrier, dicarboxylate transporter), member 10 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20210128 MGI 732071 Slc25a10 solute carrier family 25 (mitochondrial carrier, dicarboxylate transporter), member 10 gene MP:0010052 increased grip strength IEA N RGD:5509061 20181227 MGI 732071 Slc25a10 solute carrier family 25 (mitochondrial carrier, dicarboxylate transporter), member 10 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20210520 MGI 732071 Slc25a10 solute carrier family 25 (mitochondrial carrier, dicarboxylate transporter), member 10 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12642602 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12642602 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:12642602 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12642602 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20170713 MGI PMID:27629921 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20210128 MGI 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12642602 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:12642602 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12642602 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0008609 decreased circulating interleukin-13 level IAGP N RGD:5509061 20141003 MGI PMID:12642602 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:12642602 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:12642602 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12642602 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:12642602 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20170713 MGI PMID:27629921 732072 Il13ra2 interleukin 13 receptor, alpha 2 gene MP:0030002 increased lung apoptosis IAGP N RGD:5509061 20170713 MGI PMID:27629921 732074 Gps1 G protein pathway suppressor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 732074 Gps1 G protein pathway suppressor 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 732074 Gps1 G protein pathway suppressor 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 732076 Sdc3 syndecan 3 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:11461706 732076 Sdc3 syndecan 3 gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20201022 MGI 732076 Sdc3 syndecan 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15520868 732076 Sdc3 syndecan 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15520868 732076 Sdc3 syndecan 3 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:15520868 732076 Sdc3 syndecan 3 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:15520868 732076 Sdc3 syndecan 3 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:15520868 732076 Sdc3 syndecan 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15520868 732076 Sdc3 syndecan 3 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:15520868 732076 Sdc3 syndecan 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20201022 MGI 732079 Plat plasminogen activator, tissue gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 732079 Plat plasminogen activator, tissue gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 732079 Plat plasminogen activator, tissue gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20141003 MGI PMID:8133887 732079 Plat plasminogen activator, tissue gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:8133887 732079 Plat plasminogen activator, tissue gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170105 MGI 732079 Plat plasminogen activator, tissue gene MP:0001147 small testis IEA N RGD:5509061 20170105 MGI 732079 Plat plasminogen activator, tissue gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8133887 732079 Plat plasminogen activator, tissue gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8133887 732079 Plat plasminogen activator, tissue gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:8133887 732079 Plat plasminogen activator, tissue gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12524546 732079 Plat plasminogen activator, tissue gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15522965 732079 Plat plasminogen activator, tissue gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:10762331 732079 Plat plasminogen activator, tissue gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:10762331 732079 Plat plasminogen activator, tissue gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:10762331 732079 Plat plasminogen activator, tissue gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10762331 732079 Plat plasminogen activator, tissue gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8133887 732079 Plat plasminogen activator, tissue gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:12524546 732079 Plat plasminogen activator, tissue gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15522965 732079 Plat plasminogen activator, tissue gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:10762331 732079 Plat plasminogen activator, tissue gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:12524546 732079 Plat plasminogen activator, tissue gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:15522965 732079 Plat plasminogen activator, tissue gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14630814 732079 Plat plasminogen activator, tissue gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:8133887 732079 Plat plasminogen activator, tissue gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8133887 732079 Plat plasminogen activator, tissue gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:8133887 732079 Plat plasminogen activator, tissue gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8133887 732079 Plat plasminogen activator, tissue gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15631996 732079 Plat plasminogen activator, tissue gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:10762331 732079 Plat plasminogen activator, tissue gene MP:0002798 abnormal active avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:10762331 732079 Plat plasminogen activator, tissue gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:12917371 732079 Plat plasminogen activator, tissue gene MP:0002935 chronic joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:11891190 732079 Plat plasminogen activator, tissue gene MP:0002936 joint swelling IAGP N RGD:5509061 20141003 MGI PMID:11891190 732079 Plat plasminogen activator, tissue gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:11891190 732079 Plat plasminogen activator, tissue gene MP:0003075 abnormal response to CNS ischemic injury IAGP N RGD:5509061 20141003 MGI PMID:19147818 732079 Plat plasminogen activator, tissue gene MP:0003423 reduced thrombolysis IAGP N RGD:5509061 20141003 MGI PMID:10961882 732079 Plat plasminogen activator, tissue gene MP:0003423 reduced thrombolysis IAGP N RGD:5509061 20141003 MGI PMID:8133887 732079 Plat plasminogen activator, tissue gene MP:0003426 pulmonary interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10880388 732079 Plat plasminogen activator, tissue gene MP:0003434 decreased susceptibility to induced choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:12657615 732079 Plat plasminogen activator, tissue gene MP:0003455 decreased susceptibility to induced retina damage IAGP N RGD:5509061 20141003 MGI PMID:15451307 732079 Plat plasminogen activator, tissue gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19147818 732079 Plat plasminogen activator, tissue gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:8133887 732079 Plat plasminogen activator, tissue gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:8133887 732079 Plat plasminogen activator, tissue gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:10880388 732079 Plat plasminogen activator, tissue gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15631996 732079 Plat plasminogen activator, tissue gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11557572 732079 Plat plasminogen activator, tissue gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15631996 732079 Plat plasminogen activator, tissue gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:14988509 732079 Plat plasminogen activator, tissue gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:10318667 732079 Plat plasminogen activator, tissue gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:11891190 732079 Plat plasminogen activator, tissue gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:9576763 732079 Plat plasminogen activator, tissue gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:14988509 732079 Plat plasminogen activator, tissue gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20141003 MGI PMID:14988509 732079 Plat plasminogen activator, tissue gene MP:0010211 abnormal acute phase protein level IAGP N RGD:5509061 20141003 MGI PMID:10880388 732079 Plat plasminogen activator, tissue gene MP:0010211 abnormal acute phase protein level IAGP N RGD:5509061 20141003 MGI PMID:11891190 732079 Plat plasminogen activator, tissue gene MP:0010211 abnormal acute phase protein level IAGP N RGD:5509061 20141003 MGI PMID:12657615 732079 Plat plasminogen activator, tissue gene MP:0010909 pulmonary alveolar hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10880388 732079 Plat plasminogen activator, tissue gene MP:0020948 abnormal susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200625 MGI PMID:23919993 732079 Plat plasminogen activator, tissue gene MP:0030006 decreased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:15451307 732079 Plat plasminogen activator, tissue gene MP:0030530 abnormal outer ear skin morphology IAGP N RGD:5509061 20180118 MGI PMID:8133887 732079 Plat plasminogen activator, tissue gene MP:0030531 abnormal facial skin morphology IAGP N RGD:5509061 20180118 MGI PMID:8133887 732079 Plat plasminogen activator, tissue gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200625 MGI PMID:23919993 732079 Plat plasminogen activator, tissue gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:8133887 732080 Vamp5 vesicle-associated membrane protein 5 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20180719 MGI PMID:29330887 732080 Vamp5 vesicle-associated membrane protein 5 gene MP:0000536 hydroureter IAGP N RGD:5509061 20180719 MGI PMID:29330887 732080 Vamp5 vesicle-associated membrane protein 5 gene MP:0001177 atelectasis IAGP N RGD:5509061 20180719 MGI PMID:29330887 732080 Vamp5 vesicle-associated membrane protein 5 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20180719 MGI PMID:29330887 732080 Vamp5 vesicle-associated membrane protein 5 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20180719 MGI PMID:29330887 732080 Vamp5 vesicle-associated membrane protein 5 gene MP:0003586 dilated ureter IAGP N RGD:5509061 20180719 MGI PMID:29330887 732080 Vamp5 vesicle-associated membrane protein 5 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20180719 MGI PMID:29330887 732080 Vamp5 vesicle-associated membrane protein 5 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20180719 MGI PMID:29330887 732080 Vamp5 vesicle-associated membrane protein 5 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20180719 MGI PMID:29330887 732080 Vamp5 vesicle-associated membrane protein 5 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:29330887 732080 Vamp5 vesicle-associated membrane protein 5 gene MP:0011493 double ureter IAGP N RGD:5509061 20180719 MGI PMID:29330887 732081 Ffar1 free fatty acid receptor 1 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18678612 732081 Ffar1 free fatty acid receptor 1 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18678612 732081 Ffar1 free fatty acid receptor 1 gene MP:0001985 abnormal gustatory system physiology IAGP N RGD:5509061 20141003 MGI PMID:20573884 732081 Ffar1 free fatty acid receptor 1 gene MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20573884 732081 Ffar1 free fatty acid receptor 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18678612 732081 Ffar1 free fatty acid receptor 1 gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:18678612 732081 Ffar1 free fatty acid receptor 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16054069 732081 Ffar1 free fatty acid receptor 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16054069 732081 Ffar1 free fatty acid receptor 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:16054069 732081 Ffar1 free fatty acid receptor 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17395749 732081 Ffar1 free fatty acid receptor 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:16054069 732081 Ffar1 free fatty acid receptor 1 gene MP:0003565 abnormal glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:23403053 732081 Ffar1 free fatty acid receptor 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16054069 732081 Ffar1 free fatty acid receptor 1 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:18678612 732081 Ffar1 free fatty acid receptor 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23403053 732081 Ffar1 free fatty acid receptor 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18678612 732081 Ffar1 free fatty acid receptor 1 gene MP:0010055 abnormal sensory neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:20573884 732081 Ffar1 free fatty acid receptor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 732081 Ffar1 free fatty acid receptor 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:18678612 732081 Ffar1 free fatty acid receptor 1 gene MP:0011969 abnormal circulating triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:16054069 732081 Ffar1 free fatty acid receptor 1 gene MP:0014125 decreased amylin secretion IAGP N RGD:5509061 20160324 MGI PMID:18678612 732081 Ffar1 free fatty acid receptor 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:16054069 732085 Cth cystathionine gamma lyase gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:18948540 732085 Cth cystathionine gamma lyase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 732085 Cth cystathionine gamma lyase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 732085 Cth cystathionine gamma lyase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 732085 Cth cystathionine gamma lyase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210520 MGI 732085 Cth cystathionine gamma lyase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 732085 Cth cystathionine gamma lyase gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0002965 increased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0004065 increased susceptibility to induced muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0005571 decreased lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:18948540 732085 Cth cystathionine gamma lyase gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18948540 732085 Cth cystathionine gamma lyase gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18948540 732085 Cth cystathionine gamma lyase gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 732085 Cth cystathionine gamma lyase gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20180913 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20180920 MGI PMID:18948540 732085 Cth cystathionine gamma lyase gene MP:0012604 decreased glutathione level IAGP N RGD:5509061 20180920 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0030626 decreased circulating cysteine level IAGP N RGD:5509061 20180920 MGI PMID:18948540 732085 Cth cystathionine gamma lyase gene MP:0030639 decreased circulating taurine level IAGP N RGD:5509061 20180913 MGI PMID:20566639 732085 Cth cystathionine gamma lyase gene MP:0030689 cystathioninuria IAGP N RGD:5509061 20180920 MGI PMID:20566639 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170824 MGI PMID:20008274 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:9363893 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:9363893 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9363893 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:10749873 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20170824 MGI PMID:20008274 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:12740571 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0001853 heart inflammation IAGP N RGD:5509061 20170824 MGI PMID:20008274 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:11782353 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15354288 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15354288 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9600059 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15354288 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:9600059 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12208866 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:9600059 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20170824 MGI PMID:20008274 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170824 MGI PMID:20008274 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0002833 increased heart weight IAGP N RGD:5509061 20170824 MGI PMID:20008274 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0003035 decreased pulmonary vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:9363893 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15354288 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:9363893 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:9600059 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:12208866 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20141003 MGI PMID:12208866 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:9363893 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:9600059 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:9363893 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0004038 lymphangiectasis IAGP N RGD:5509061 20141003 MGI PMID:9363893 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16303601 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11782353 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12740571 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170824 MGI PMID:20008274 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:9600059 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12740571 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20170824 MGI PMID:20008274 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:12740571 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:9363893 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:9600059 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:10749873 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12740571 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0008595 abnormal circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:12208866 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:12208866 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:9600059 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0009811 abnormal prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:12208866 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:9363893 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:9600059 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:9363893 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0010214 abnormal circulating serum amyloid protein level IAGP N RGD:5509061 20141003 MGI PMID:12208866 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0010557 dilated pulmonary artery IAGP N RGD:5509061 20141003 MGI PMID:9600059 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20170824 MGI PMID:20008274 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0010909 pulmonary alveolar hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9363893 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9363893 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20170824 MGI PMID:20008274 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231221 MGI PMID:20008274 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:9363893 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:9363893 732089 Ptger4 prostaglandin E receptor 4 (subtype EP4) gene MP:0031129 left-to-right shunt IAGP N RGD:5509061 20201015 MGI PMID:9363893 732090 Palm paralemmin gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 732090 Palm paralemmin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240502 MGI PMID:23709172 732090 Palm paralemmin gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 732090 Palm paralemmin gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20240502 MGI PMID:23709172 732092 Fzd2 frizzled class receptor 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:23095888 732092 Fzd2 frizzled class receptor 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23095888 732092 Fzd2 frizzled class receptor 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:23095888 732092 Fzd2 frizzled class receptor 2 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:23095888 732092 Fzd2 frizzled class receptor 2 gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:23095888 732092 Fzd2 frizzled class receptor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 732092 Fzd2 frizzled class receptor 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23095888 732092 Fzd2 frizzled class receptor 2 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:23095888 732092 Fzd2 frizzled class receptor 2 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:23095888 732092 Fzd2 frizzled class receptor 2 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:23095888 732092 Fzd2 frizzled class receptor 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23095888 732092 Fzd2 frizzled class receptor 2 gene MP:0004406 abnormal cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:23095888 732092 Fzd2 frizzled class receptor 2 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23095888 732092 Fzd2 frizzled class receptor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23095888 732092 Fzd2 frizzled class receptor 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20940229 732092 Fzd2 frizzled class receptor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23095888 732092 Fzd2 frizzled class receptor 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210422 MGI 732092 Fzd2 frizzled class receptor 2 gene MP:0011203 abnormal parietal yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:23095888 732092 Fzd2 frizzled class receptor 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20221103 MGI 732092 Fzd2 frizzled class receptor 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 732095 Pcna proliferating cell nuclear antigen gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18854411 732095 Pcna proliferating cell nuclear antigen gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18854411 732095 Pcna proliferating cell nuclear antigen gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23201573 732095 Pcna proliferating cell nuclear antigen gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:17664295 732095 Pcna proliferating cell nuclear antigen gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:18854411 732095 Pcna proliferating cell nuclear antigen gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:18854411 732095 Pcna proliferating cell nuclear antigen gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23201573 732095 Pcna proliferating cell nuclear antigen gene MP:0004806 absent germ cells IAGP N RGD:5509061 20141003 MGI PMID:17664295 732095 Pcna proliferating cell nuclear antigen gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:17664295 732095 Pcna proliferating cell nuclear antigen gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:18854411 732095 Pcna proliferating cell nuclear antigen gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:19901081 732095 Pcna proliferating cell nuclear antigen gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20180125 MGI PMID:21269891 732095 Pcna proliferating cell nuclear antigen gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:18854411 732095 Pcna proliferating cell nuclear antigen gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:23201573 732095 Pcna proliferating cell nuclear antigen gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:23201573 732095 Pcna proliferating cell nuclear antigen gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:23201573 732095 Pcna proliferating cell nuclear antigen gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18854411 732095 Pcna proliferating cell nuclear antigen gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17664295 732095 Pcna proliferating cell nuclear antigen gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20141003 MGI PMID:23201573 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0001260 increased body weight IEA N RGD:5509061 20111116 MGI 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16554468 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15159536 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:20468048 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20468048 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0002634 abnormal sensorimotor gating IAGP N RGD:5509061 20141003 MGI PMID:15159536 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0002798 abnormal active avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:16554468 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:16554468 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15159536 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0003234 enhanced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15555781 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0003234 enhanced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16554468 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15159536 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:20468048 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:20468048 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0006299 abnormal latent inhibition of conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16554468 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:16554468 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20468048 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14622582 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15159536 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20468048 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15555781 732097 Slc6a9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 732099 Fut9 fucosyltransferase 9 gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23986452 732099 Fut9 fucosyltransferase 9 gene MP:0012206 increased neuronal stem cell self-renewal IAGP N RGD:5509061 20141003 MGI PMID:23986452 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12612061 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0010568 abnormal bulbus cordis morphology IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0012510 abnormal aortic sac morphology IAGP N RGD:5509061 20141003 MGI PMID:18948620 732102 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2 gene MP:0012511 dilated aortic sac IAGP N RGD:5509061 20141003 MGI PMID:18948620 732104 Metap2 methionine aminopeptidase 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:16790550 732104 Metap2 methionine aminopeptidase 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16790550 732104 Metap2 methionine aminopeptidase 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16790550 732104 Metap2 methionine aminopeptidase 2 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:16790550 732104 Metap2 methionine aminopeptidase 2 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:16790550 732104 Metap2 methionine aminopeptidase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16790550 732104 Metap2 methionine aminopeptidase 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16790550 732104 Metap2 methionine aminopeptidase 2 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:16790550 732104 Metap2 methionine aminopeptidase 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16790550 732104 Metap2 methionine aminopeptidase 2 gene MP:0006057 decreased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:16790550 732104 Metap2 methionine aminopeptidase 2 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16790550 732104 Metap2 methionine aminopeptidase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16790550 732104 Metap2 methionine aminopeptidase 2 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16790550 732104 Metap2 methionine aminopeptidase 2 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:16790550 732106 Fadd Fas associated via death domain gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9506948 732106 Fadd Fas associated via death domain gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21115735 732106 Fadd Fas associated via death domain gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20141003 MGI PMID:21804564 732106 Fadd Fas associated via death domain gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:21804564 732106 Fadd Fas associated via death domain gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:21804564 732106 Fadd Fas associated via death domain gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:21804564 732106 Fadd Fas associated via death domain gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:21804564 732106 Fadd Fas associated via death domain gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20615958 732106 Fadd Fas associated via death domain gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21115735 732106 Fadd Fas associated via death domain gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:20615958 732106 Fadd Fas associated via death domain gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20190502 MGI 732106 Fadd Fas associated via death domain gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21804564 732106 Fadd Fas associated via death domain gene MP:0001586 abnormal erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20615958 732106 Fadd Fas associated via death domain gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9506948 732106 Fadd Fas associated via death domain gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 732106 Fadd Fas associated via death domain gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9506948 732106 Fadd Fas associated via death domain gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11353862 732106 Fadd Fas associated via death domain gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21115735 732106 Fadd Fas associated via death domain gene MP:0001830 decreased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:16116191 732106 Fadd Fas associated via death domain gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:17292824 732106 Fadd Fas associated via death domain gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11353862 732106 Fadd Fas associated via death domain gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:21115735 732106 Fadd Fas associated via death domain gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21115735 732106 Fadd Fas associated via death domain gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:9506948 732106 Fadd Fas associated via death domain gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:21804564 732106 Fadd Fas associated via death domain gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17292824 732106 Fadd Fas associated via death domain gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20201231 MGI 732106 Fadd Fas associated via death domain gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:20615958 732106 Fadd Fas associated via death domain gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 732106 Fadd Fas associated via death domain gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9506948 732106 Fadd Fas associated via death domain gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21068410 732106 Fadd Fas associated via death domain gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11353862 732106 Fadd Fas associated via death domain gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16116191 732106 Fadd Fas associated via death domain gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20615958 732106 Fadd Fas associated via death domain gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:20615958 732106 Fadd Fas associated via death domain gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:21804564 732106 Fadd Fas associated via death domain gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:11353862 732106 Fadd Fas associated via death domain gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11353862 732106 Fadd Fas associated via death domain gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20615958 732106 Fadd Fas associated via death domain gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9506948 732106 Fadd Fas associated via death domain gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17292824 732106 Fadd Fas associated via death domain gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17292824 732106 Fadd Fas associated via death domain gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11353862 732106 Fadd Fas associated via death domain gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11353862 732106 Fadd Fas associated via death domain gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16116191 732106 Fadd Fas associated via death domain gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:21068410 732106 Fadd Fas associated via death domain gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21804564 732106 Fadd Fas associated via death domain gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21804564 732106 Fadd Fas associated via death domain gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21804564 732106 Fadd Fas associated via death domain gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:16116191 732106 Fadd Fas associated via death domain gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:10862756 732106 Fadd Fas associated via death domain gene MP:0009258 abnormal thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20615958 732106 Fadd Fas associated via death domain gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20141003 MGI PMID:21804564 732106 Fadd Fas associated via death domain gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20221215 MGI 732106 Fadd Fas associated via death domain gene MP:0010205 abnormal oligodendrocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21068410 732106 Fadd Fas associated via death domain gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21804564 732106 Fadd Fas associated via death domain gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9521326 732106 Fadd Fas associated via death domain gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9506948 732106 Fadd Fas associated via death domain gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 732106 Fadd Fas associated via death domain gene MP:0013486 decreased Paneth cell number IAGP N RGD:5509061 20150312 MGI PMID:21804564 732106 Fadd Fas associated via death domain gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:9506948 732107 Agpat4 1-acylglycerol-3-phosphate O-acyltransferase 4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170323 MGI 732107 Agpat4 1-acylglycerol-3-phosphate O-acyltransferase 4 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 732107 Agpat4 1-acylglycerol-3-phosphate O-acyltransferase 4 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 732107 Agpat4 1-acylglycerol-3-phosphate O-acyltransferase 4 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20170323 MGI PMID:26417903 732107 Agpat4 1-acylglycerol-3-phosphate O-acyltransferase 4 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20170105 MGI 732107 Agpat4 1-acylglycerol-3-phosphate O-acyltransferase 4 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 732107 Agpat4 1-acylglycerol-3-phosphate O-acyltransferase 4 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 732108 Tub TUB bipartite transcription factor gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:7612867 732108 Tub TUB bipartite transcription factor gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:24316073 732108 Tub TUB bipartite transcription factor gene MP:0001260 increased body weight IEA N RGD:5509061 20150702 MGI 732108 Tub TUB bipartite transcription factor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:8606774 732108 Tub TUB bipartite transcription factor gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:10629044 732108 Tub TUB bipartite transcription factor gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:10629044 732108 Tub TUB bipartite transcription factor gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:7479945 732108 Tub TUB bipartite transcription factor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:8177042 732108 Tub TUB bipartite transcription factor gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:8606774 732108 Tub TUB bipartite transcription factor gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20210909 MGI PMID:11925566 732108 Tub TUB bipartite transcription factor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:8606774 732108 Tub TUB bipartite transcription factor gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20210916 MGI PMID:22323461 732108 Tub TUB bipartite transcription factor gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:8606774 732108 Tub TUB bipartite transcription factor gene MP:0002628 hepatic steatosis IEA N RGD:5509061 20111116 MGI 732108 Tub TUB bipartite transcription factor gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:7479945 732108 Tub TUB bipartite transcription factor gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:7612867 732108 Tub TUB bipartite transcription factor gene MP:0003151 absent tunnel of Corti IAGP N RGD:5509061 20141003 MGI PMID:7612867 732108 Tub TUB bipartite transcription factor gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:10629044 732108 Tub TUB bipartite transcription factor gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7612867 732108 Tub TUB bipartite transcription factor gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:7479945 732108 Tub TUB bipartite transcription factor gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:7612867 732108 Tub TUB bipartite transcription factor gene MP:0004289 abnormal bony labyrinth IAGP N RGD:5509061 20141003 MGI PMID:7612867 732108 Tub TUB bipartite transcription factor gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:7612867 732108 Tub TUB bipartite transcription factor gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:7479945 732108 Tub TUB bipartite transcription factor gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:7479945 732108 Tub TUB bipartite transcription factor gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:7612867 732108 Tub TUB bipartite transcription factor gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:7479945 732108 Tub TUB bipartite transcription factor gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:7612867 732108 Tub TUB bipartite transcription factor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177042 732108 Tub TUB bipartite transcription factor gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7479945 732108 Tub TUB bipartite transcription factor gene MP:0005362 abnormal Langerhans cell physiology IEA N RGD:5509061 20111116 MGI 732108 Tub TUB bipartite transcription factor gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:10629044 732108 Tub TUB bipartite transcription factor gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7479945 732108 Tub TUB bipartite transcription factor gene MP:0006187 retina deposits IAGP N RGD:5509061 20141003 MGI PMID:7479945 732108 Tub TUB bipartite transcription factor gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:7479945 732108 Tub TUB bipartite transcription factor gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:8606774 732108 Tub TUB bipartite transcription factor gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:11481257 732108 Tub TUB bipartite transcription factor gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:7479945 732108 Tub TUB bipartite transcription factor gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:10629044 732108 Tub TUB bipartite transcription factor gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:7479945 732108 Tub TUB bipartite transcription factor gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:11481257 732108 Tub TUB bipartite transcription factor gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:7612867 732108 Tub TUB bipartite transcription factor gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:11481257 732108 Tub TUB bipartite transcription factor gene MP:0009171 enlarged pancreatic islets IEA N RGD:5509061 20111116 MGI 732108 Tub TUB bipartite transcription factor gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20111116 MGI 732108 Tub TUB bipartite transcription factor gene MP:0010400 increased liver glycogen level IEA N RGD:5509061 20150611 MGI 732108 Tub TUB bipartite transcription factor gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:8606774 732108 Tub TUB bipartite transcription factor gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:7479945 732108 Tub TUB bipartite transcription factor gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20180913 MGI PMID:10441341 732108 Tub TUB bipartite transcription factor gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20141003 MGI PMID:7479945 732108 Tub TUB bipartite transcription factor gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:10629044 732108 Tub TUB bipartite transcription factor gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:7479945 732108 Tub TUB bipartite transcription factor gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:8606774 732110 Nip7 NIP7, nucleolar pre-rRNA processing protein gene MP:0008762 embryonic lethality IEA N RGD:5509061 20141003 MGI 732113 Ttl tubulin tyrosine ligase gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:15899979 732113 Ttl tubulin tyrosine ligase gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:15899979 732113 Ttl tubulin tyrosine ligase gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15899979 732113 Ttl tubulin tyrosine ligase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 732113 Ttl tubulin tyrosine ligase gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 732113 Ttl tubulin tyrosine ligase gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:15899979 732113 Ttl tubulin tyrosine ligase gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:15899979 732113 Ttl tubulin tyrosine ligase gene MP:0008129 absent brain internal capsule IAGP N RGD:5509061 20141003 MGI PMID:15899979 732113 Ttl tubulin tyrosine ligase gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15899979 732113 Ttl tubulin tyrosine ligase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15899979 732113 Ttl tubulin tyrosine ligase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 732117 Capn8 calpain 8 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:20686710 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0002217 small lymph nodes IEA N RGD:5509061 20160811 MGI 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20160811 MGI 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20160421 MGI 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20240104 MGI PMID:37628590 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20190926 MGI PMID:31257146 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20160421 MGI 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20181227 MGI 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20190926 MGI PMID:31257146 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20190926 MGI PMID:31257146 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20190926 MGI PMID:31257146 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20240104 MGI PMID:37628590 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0009701 abnormal birth body size IAGP N RGD:5509061 20240104 MGI PMID:37628590 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:31257146 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0020870 decreased thigmotaxis IAGP N RGD:5509061 20240104 MGI PMID:37628590 732121 Atp6v1b2 ATPase, H+ transporting, lysosomal V1 subunit B2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20240104 MGI PMID:37628590 732124 Gp1bb glycoprotein Ib, beta polypeptide gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 732124 Gp1bb glycoprotein Ib, beta polypeptide gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20181227 MGI 732124 Gp1bb glycoprotein Ib, beta polypeptide gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 732124 Gp1bb glycoprotein Ib, beta polypeptide gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 732124 Gp1bb glycoprotein Ib, beta polypeptide gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:15213102 732124 Gp1bb glycoprotein Ib, beta polypeptide gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:15213102 732124 Gp1bb glycoprotein Ib, beta polypeptide gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17095718 732124 Gp1bb glycoprotein Ib, beta polypeptide gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:17095718 732124 Gp1bb glycoprotein Ib, beta polypeptide gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:15213102 732124 Gp1bb glycoprotein Ib, beta polypeptide gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:17095718 732124 Gp1bb glycoprotein Ib, beta polypeptide gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 732124 Gp1bb glycoprotein Ib, beta polypeptide gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:17095718 732127 Cacng3 calcium channel, voltage-dependent, gamma subunit 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18753375 732127 Cacng3 calcium channel, voltage-dependent, gamma subunit 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18753375 732127 Cacng3 calcium channel, voltage-dependent, gamma subunit 3 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20111116 MGI 732127 Cacng3 calcium channel, voltage-dependent, gamma subunit 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18753375 732127 Cacng3 calcium channel, voltage-dependent, gamma subunit 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:18753375 732127 Cacng3 calcium channel, voltage-dependent, gamma subunit 3 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18753375 732127 Cacng3 calcium channel, voltage-dependent, gamma subunit 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18753375 732127 Cacng3 calcium channel, voltage-dependent, gamma subunit 3 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20111116 MGI 732127 Cacng3 calcium channel, voltage-dependent, gamma subunit 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18753375 732129 Il11 interleukin 11 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0001926 female infertility IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0008588 abnormal circulating interleukin level IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0009130 increased white fat cell number IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0011720 abnormal ossification involved in bone remodeling IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0021186 decreased bone mineral density of vertebrae IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0030009 increased bone marrow adipose tissue amount IAGP N RGD:5509061 20240627 MGI PMID:36424386 732129 Il11 interleukin 11 gene MP:0030985 decreased circulating osteocalcin level IAGP N RGD:5509061 20240627 MGI PMID:36424386 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0000599 enlarged liver IEA N RGD:5509061 20210520 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0001148 enlarged testis IEA N RGD:5509061 20210826 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10629036 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210826 MGI 732131 Gna15 guanine nucleotide binding protein, alpha 15 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210520 MGI 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20190808 MGI PMID:24465224 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20190808 MGI PMID:24465224 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20210520 MGI 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20190808 MGI PMID:24465224 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0009826 abnormal dermis reticular layer collagen network IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20363744 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20170105 MGI 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20190808 MGI PMID:24465224 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20190808 MGI PMID:24465224 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20190808 MGI PMID:24465224 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0011642 abnormal bone collagen fibril morphology IAGP N RGD:5509061 20190808 MGI PMID:24465224 732133 P3h1 prolyl 3-hydroxylase 1 gene MP:0012000 abnormal limb position IEA N RGD:5509061 20170105 MGI 732134 Crlf3 cytokine receptor-like factor 3 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 732134 Crlf3 cytokine receptor-like factor 3 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20160421 MGI 732134 Crlf3 cytokine receptor-like factor 3 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20141003 MGI 732134 Crlf3 cytokine receptor-like factor 3 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23870131 732134 Crlf3 cytokine receptor-like factor 3 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160804 MGI 732134 Crlf3 cytokine receptor-like factor 3 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 732134 Crlf3 cytokine receptor-like factor 3 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 732134 Crlf3 cytokine receptor-like factor 3 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20240314 MGI PMID:37712888 732134 Crlf3 cytokine receptor-like factor 3 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 732134 Crlf3 cytokine receptor-like factor 3 gene MP:0021090 abnormal dendrite arborization pattern IAGP N RGD:5509061 20240314 MGI PMID:37712888 732135 Lrit1 leucine-rich repeat, immunoglobulin-like and transmembrane domains 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20180503 MGI PMID:29590623 732135 Lrit1 leucine-rich repeat, immunoglobulin-like and transmembrane domains 1 gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20180503 MGI PMID:29590623 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11884418 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20221215 MGI 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20181227 MGI 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19660563 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20180301 MGI PMID:25534853 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11884418 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20180301 MGI PMID:25534853 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180301 MGI PMID:25534853 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20180301 MGI PMID:25534853 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180301 MGI PMID:25534853 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11884418 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180301 MGI PMID:25534853 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20180301 MGI PMID:25534853 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:19660563 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0009122 decreased white fat cell lipid droplet size IAGP N RGD:5509061 20180301 MGI PMID:25534853 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20180301 MGI PMID:25534853 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20180301 MGI PMID:25534853 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0011016 increased core body temperature IAGP N RGD:5509061 20180301 MGI PMID:25534853 732138 Lnpep leucyl/cystinyl aminopeptidase gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:25534853 732140 Il12a interleukin 12a gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20201022 MGI 732140 Il12a interleukin 12a gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17082625 732140 Il12a interleukin 12a gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17082625 732140 Il12a interleukin 12a gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16688182 732140 Il12a interleukin 12a gene MP:0004609 vertebral fusion IEA N RGD:5509061 20170105 MGI 732140 Il12a interleukin 12a gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:17277169 732140 Il12a interleukin 12a gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:8766560 732140 Il12a interleukin 12a gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17389237 732140 Il12a interleukin 12a gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8766560 732140 Il12a interleukin 12a gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:8766560 732140 Il12a interleukin 12a gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20141003 MGI PMID:17082625 732140 Il12a interleukin 12a gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:10209048 732140 Il12a interleukin 12a gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:12370359 732140 Il12a interleukin 12a gene MP:0008618 decreased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:10209048 732140 Il12a interleukin 12a gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15240709 732140 Il12a interleukin 12a gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12370359 732140 Il12a interleukin 12a gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18656388 732140 Il12a interleukin 12a gene MP:0020916 increased susceptibility to Herpesvirales infection IEA N RGD:5509061 20200430 MGI 732141 Txnip thioredoxin interacting protein gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 732141 Txnip thioredoxin interacting protein gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:18322014 732141 Txnip thioredoxin interacting protein gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20160421 MGI 732141 Txnip thioredoxin interacting protein gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 732141 Txnip thioredoxin interacting protein gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18322014 732141 Txnip thioredoxin interacting protein gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9537422 732141 Txnip thioredoxin interacting protein gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 732141 Txnip thioredoxin interacting protein gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18322014 732141 Txnip thioredoxin interacting protein gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15173414 732141 Txnip thioredoxin interacting protein gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17143286 732141 Txnip thioredoxin interacting protein gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:18322014 732141 Txnip thioredoxin interacting protein gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:15723808 732141 Txnip thioredoxin interacting protein gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:18322014 732141 Txnip thioredoxin interacting protein gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20160421 MGI 732141 Txnip thioredoxin interacting protein gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:15173414 732141 Txnip thioredoxin interacting protein gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16607285 732141 Txnip thioredoxin interacting protein gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:18322014 732141 Txnip thioredoxin interacting protein gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17916779 732141 Txnip thioredoxin interacting protein gene MP:0003926 decreased cellular glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:18322014 732141 Txnip thioredoxin interacting protein gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:17916779 732141 Txnip thioredoxin interacting protein gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:15723808 732141 Txnip thioredoxin interacting protein gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15723808 732141 Txnip thioredoxin interacting protein gene MP:0005068 abnormal NK cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15723808 732141 Txnip thioredoxin interacting protein gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9537422 732141 Txnip thioredoxin interacting protein gene MP:0005161 hematuria IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9537422 732141 Txnip thioredoxin interacting protein gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:15723808 732141 Txnip thioredoxin interacting protein gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15173414 732141 Txnip thioredoxin interacting protein gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18322014 732141 Txnip thioredoxin interacting protein gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15723808 732141 Txnip thioredoxin interacting protein gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17916779 732141 Txnip thioredoxin interacting protein gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0005634 decreased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0006084 abnormal circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:15723808 732141 Txnip thioredoxin interacting protein gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:15723808 732141 Txnip thioredoxin interacting protein gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15723808 732141 Txnip thioredoxin interacting protein gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18322014 732141 Txnip thioredoxin interacting protein gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 732141 Txnip thioredoxin interacting protein gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 732141 Txnip thioredoxin interacting protein gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15723808 732141 Txnip thioredoxin interacting protein gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:18322014 732141 Txnip thioredoxin interacting protein gene MP:0012325 decreased circulating antithrombin level IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0012356 increased prothrombin time IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0012359 increased partial thromboplastin time IAGP N RGD:5509061 20141003 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:18322014 732141 Txnip thioredoxin interacting protein gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:17916779 732141 Txnip thioredoxin interacting protein gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:16254043 732141 Txnip thioredoxin interacting protein gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:18322014 732141 Txnip thioredoxin interacting protein gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:17916779 732142 Bst1 bone marrow stromal cell antigen 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:9780166 732142 Bst1 bone marrow stromal cell antigen 1 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:9780166 732142 Bst1 bone marrow stromal cell antigen 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9780166 732142 Bst1 bone marrow stromal cell antigen 1 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:9780166 732142 Bst1 bone marrow stromal cell antigen 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9780166 732142 Bst1 bone marrow stromal cell antigen 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9780166 732142 Bst1 bone marrow stromal cell antigen 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9780166 732143 S100a6 S100 calcium binding protein A6 (calcyclin) gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220519 MGI 732143 S100a6 S100 calcium binding protein A6 (calcyclin) gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20231207 MGI 732143 S100a6 S100 calcium binding protein A6 (calcyclin) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 732143 S100a6 S100 calcium binding protein A6 (calcyclin) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19033438 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0002861 abnormal tail bud morphology IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:19033438 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:19033438 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:19033438 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210520 MGI 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19033438 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0011230 abnormal folic acid level IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0012062 small tail bud IAGP N RGD:5509061 20141003 MGI PMID:23704330 732148 Mthfd1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 732150 Dhrs4 dehydrogenase/reductase 4 gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20141003 MGI 732150 Dhrs4 dehydrogenase/reductase 4 gene MP:0002573 behavioral despair IEA N RGD:5509061 20141003 MGI 732150 Dhrs4 dehydrogenase/reductase 4 gene MP:0008496 decreased IgG2a level IEA N RGD:5509061 20141003 MGI 732152 Snap23 synaptosomal-associated protein 23 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220811 MGI 732152 Snap23 synaptosomal-associated protein 23 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20200402 MGI 732152 Snap23 synaptosomal-associated protein 23 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:21479242 732152 Snap23 synaptosomal-associated protein 23 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20118925 732152 Snap23 synaptosomal-associated protein 23 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21479242 732152 Snap23 synaptosomal-associated protein 23 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21479242 732152 Snap23 synaptosomal-associated protein 23 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 732156 Rab3ip RAB3A interacting protein gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 732156 Rab3ip RAB3A interacting protein gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 732156 Rab3ip RAB3A interacting protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7655516 732156 Rab3ip RAB3A interacting protein gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 732156 Rab3ip RAB3A interacting protein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 732156 Rab3ip RAB3A interacting protein gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20230601 MGI 732156 Rab3ip RAB3A interacting protein gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 732156 Rab3ip RAB3A interacting protein gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 732156 Rab3ip RAB3A interacting protein gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 732160 Pdcd4 programmed cell death 4 gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:17114484 732160 Pdcd4 programmed cell death 4 gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:18296647 732160 Pdcd4 programmed cell death 4 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:17114484 732160 Pdcd4 programmed cell death 4 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17114484 732160 Pdcd4 programmed cell death 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17114484 732160 Pdcd4 programmed cell death 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17114484 732160 Pdcd4 programmed cell death 4 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17114484 732160 Pdcd4 programmed cell death 4 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:17114484 732160 Pdcd4 programmed cell death 4 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:17114484 732160 Pdcd4 programmed cell death 4 gene MP:0009737 prostate gland cyst IAGP N RGD:5509061 20141003 MGI PMID:17114484 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:619449 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:6512240 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0000706 small thymus IEA N RGD:5509061 20220519 MGI 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0000745 tremors IEA N RGD:5509061 20210128 MGI 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20220519 MGI 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:619449 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:6512240 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:6512240 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:6512240 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:6512240 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:6512240 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:6512240 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:15109702 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:6512240 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:6512240 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:619449 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:6512240 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0002764 short tibia IEA N RGD:5509061 20190502 MGI 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20220519 MGI 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20141003 MGI PMID:15109702 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20141003 MGI PMID:6512240 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20220519 MGI 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:619449 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:619449 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:619449 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0004047 abnormal milk composition IEA N RGD:5509061 20200102 MGI 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0004812 abnormal linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:15109702 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:15109702 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:6512240 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:619449 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0009599 thick epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:619449 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0009615 abnormal zinc homeostasis IAGP N RGD:5509061 20141003 MGI PMID:619449 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0009615 abnormal zinc homeostasis IAGP N RGD:5509061 20141003 MGI PMID:6512240 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:619449 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6512240 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0013716 hypolactation IAGP N RGD:5509061 20150611 MGI PMID:619449 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0020894 abnormal milk zinc level IAGP N RGD:5509061 20191226 MGI PMID:619449 732161 Slc30a4 solute carrier family 30 (zinc transporter), member 4 gene MP:0020894 abnormal milk zinc level IAGP N RGD:5509061 20191226 MGI PMID:6512240 732163 Doc2b double C2, beta gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:20150444 732163 Doc2b double C2, beta gene MP:0002915 abnormal synaptic depression IAGP N RGD:5509061 20241031 MGI PMID:33753311 732163 Doc2b double C2, beta gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20150444 732163 Doc2b double C2, beta gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:20150444 732163 Doc2b double C2, beta gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20241031 MGI PMID:33753311 732163 Doc2b double C2, beta gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20150444 732163 Doc2b double C2, beta gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20241031 MGI PMID:33753311 732163 Doc2b double C2, beta gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20241031 MGI PMID:33753311 732163 Doc2b double C2, beta gene MP:0008921 increased neurotransmitter release IAGP N RGD:5509061 20241031 MGI PMID:33753311 732163 Doc2b double C2, beta gene MP:0014253 decreased paired-pulse ratio IAGP N RGD:5509061 20241031 MGI PMID:33753311 732164 Htr7 5-hydroxytryptamine (serotonin) receptor 7 gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20141003 MGI PMID:17485199 732164 Htr7 5-hydroxytryptamine (serotonin) receptor 7 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12529502 732164 Htr7 5-hydroxytryptamine (serotonin) receptor 7 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12763096 732164 Htr7 5-hydroxytryptamine (serotonin) receptor 7 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 732164 Htr7 5-hydroxytryptamine (serotonin) receptor 7 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:17485199 732164 Htr7 5-hydroxytryptamine (serotonin) receptor 7 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20210128 MGI 732164 Htr7 5-hydroxytryptamine (serotonin) receptor 7 gene MP:0003858 enhanced coordination IEA N RGD:5509061 20111116 MGI 732164 Htr7 5-hydroxytryptamine (serotonin) receptor 7 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 732164 Htr7 5-hydroxytryptamine (serotonin) receptor 7 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17485199 732164 Htr7 5-hydroxytryptamine (serotonin) receptor 7 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 732167 Hdlbp high density lipoprotein (HDL) binding protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 732169 Ifi27 interferon, alpha-inducible protein 27 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:22427340 732169 Ifi27 interferon, alpha-inducible protein 27 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 732172 Bbox1 gamma-butyrobetaine hydroxylase 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 732172 Bbox1 gamma-butyrobetaine hydroxylase 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 732172 Bbox1 gamma-butyrobetaine hydroxylase 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20160811 MGI 732172 Bbox1 gamma-butyrobetaine hydroxylase 1 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20160811 MGI 732172 Bbox1 gamma-butyrobetaine hydroxylase 1 gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20160811 MGI 732172 Bbox1 gamma-butyrobetaine hydroxylase 1 gene MP:0000897 abnormal midbrain morphology IEA N RGD:5509061 20160811 MGI 732172 Bbox1 gamma-butyrobetaine hydroxylase 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 732172 Bbox1 gamma-butyrobetaine hydroxylase 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 732172 Bbox1 gamma-butyrobetaine hydroxylase 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20230601 MGI 732172 Bbox1 gamma-butyrobetaine hydroxylase 1 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20160811 MGI 732172 Bbox1 gamma-butyrobetaine hydroxylase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 732175 Bche butyrylcholinesterase gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17194517 732175 Bche butyrylcholinesterase gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17194517 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:9634237 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000262 poor arterial differentiation IAGP N RGD:5509061 20141003 MGI PMID:23395391 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20829512 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20220428 MGI PMID:31071921 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20220428 MGI PMID:31071921 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:9634238 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:9689100 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20141003 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000532 kidney vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:9689100 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9689100 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20939892 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:16166380 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11983855 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:11983855 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:12183377 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:9634238 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:9689100 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:9689100 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21124917 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9634238 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:9689100 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:9689100 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:9689100 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9689100 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001340 abnormal eyelid morphology IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21124917 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9634238 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9689100 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001603 failure of myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9634237 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21124917 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:20829512 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20220428 MGI PMID:31071921 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001785 edema IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002083 premature death IAGP N RGD:5509061 20220428 MGI PMID:31071921 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15520246 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21124917 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9634237 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12707343 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:9634238 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15520246 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9634238 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21124917 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15520246 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20220428 MGI PMID:31071921 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20141003 MGI PMID:12684531 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20141003 MGI PMID:12900445 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0003090 abnormal muscle precursor cell migration IAGP N RGD:5509061 20141003 MGI PMID:16166380 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:20939892 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0003359 hypaxial muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16166380 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20939892 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:16841089 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20220428 MGI PMID:31071921 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0004017 duplex kidney IEA N RGD:5509061 20141003 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0004158 right aortic arch IEA N RGD:5509061 20141003 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0004159 double aortic arch IEA N RGD:5509061 20141003 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:9634238 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:15520246 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12707343 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20220428 MGI PMID:31071921 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9634238 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20231207 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23395391 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20220428 MGI PMID:31071921 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20220428 MGI PMID:31071921 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0006115 aortic valve atresia IEA N RGD:5509061 20141003 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20220428 MGI PMID:31071921 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:21911833 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:21911833 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008073 abnormal CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:15189736 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:15520246 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:15520246 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21124917 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:9689100 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15520246 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12900445 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20141003 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20220428 MGI PMID:31071921 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0009119 increased brown fat cell size IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:23395391 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20141003 MGI PMID:16166380 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20829512 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9634237 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20141003 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0010428 abnormal heart right ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:20829512 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0010463 aorta stenosis IEA N RGD:5509061 20141003 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0010485 aortic arch hypoplasia IEA N RGD:5509061 20141003 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0010617 thick mitral valve cusps IAGP N RGD:5509061 20141003 MGI PMID:20829512 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21911833 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9634237 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21124917 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9634237 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9689100 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9634238 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0011518 abnormal cell chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:22438253 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0011749 perivascular fibrosis IAGP N RGD:5509061 20220428 MGI PMID:31071921 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0012568 decreased mammary gland tumor incidence in breeding females IAGP N RGD:5509061 20141003 MGI PMID:24290754 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0014145 increased white adipose tissue mass IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0014170 increased brown adipose tissue mass IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0014273 abnormal skin vasculature morphology IAGP N RGD:5509061 20230810 MGI PMID:23395391 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0020202 abnormal macrophage cell number IAGP N RGD:5509061 20180301 MGI PMID:25016030 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0020935 decreased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16841089 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0030208 abnormal intrinsic tongue muscle morphology IAGP N RGD:5509061 20171109 MGI PMID:16166380 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0031038 increased susceptibility to Retroviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:16841089 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0031155 small intestine hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:9634237 732177 Cxcr4 C-X-C motif chemokine receptor 4 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:31071921 732180 Polg polymerase (DNA directed), gamma gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:23418460 732180 Polg polymerase (DNA directed), gamma gene MP:0000248 macrocytosis IAGP N RGD:5509061 20150611 MGI PMID:19734452 732180 Polg polymerase (DNA directed), gamma gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20150611 MGI PMID:19734452 732180 Polg polymerase (DNA directed), gamma gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15888483 732180 Polg polymerase (DNA directed), gamma gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:23418460 732180 Polg polymerase (DNA directed), gamma gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23418460 732180 Polg polymerase (DNA directed), gamma gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23418460 732180 Polg polymerase (DNA directed), gamma gene MP:0002083 premature death IAGP N RGD:5509061 20150611 MGI PMID:19734452 732180 Polg polymerase (DNA directed), gamma gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20150611 MGI PMID:19734452 732180 Polg polymerase (DNA directed), gamma gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20150611 MGI PMID:19734452 732180 Polg polymerase (DNA directed), gamma gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20150611 MGI PMID:19734452 732180 Polg polymerase (DNA directed), gamma gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:16870370 732180 Polg polymerase (DNA directed), gamma gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20150611 MGI PMID:19734452 732180 Polg polymerase (DNA directed), gamma gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23418460 732180 Polg polymerase (DNA directed), gamma gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15888483 732180 Polg polymerase (DNA directed), gamma gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16870370 732180 Polg polymerase (DNA directed), gamma gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20141003 MGI PMID:16870370 732180 Polg polymerase (DNA directed), gamma gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16870370 732180 Polg polymerase (DNA directed), gamma gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:16870370 732180 Polg polymerase (DNA directed), gamma gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20150611 MGI PMID:19734452 732180 Polg polymerase (DNA directed), gamma gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20150611 MGI PMID:19734452 732180 Polg polymerase (DNA directed), gamma gene MP:0005114 premature hair loss IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23418460 732180 Polg polymerase (DNA directed), gamma gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:16870370 732180 Polg polymerase (DNA directed), gamma gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20150611 MGI PMID:19734452 732180 Polg polymerase (DNA directed), gamma gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20150611 MGI PMID:19734452 732180 Polg polymerase (DNA directed), gamma gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20150611 MGI PMID:19734452 732180 Polg polymerase (DNA directed), gamma gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20150611 MGI PMID:19734452 732180 Polg polymerase (DNA directed), gamma gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20150611 MGI PMID:19734452 732180 Polg polymerase (DNA directed), gamma gene MP:0008389 hypochromic macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23418460 732180 Polg polymerase (DNA directed), gamma gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20141003 MGI PMID:23418460 732180 Polg polymerase (DNA directed), gamma gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15888483 732180 Polg polymerase (DNA directed), gamma gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20150611 MGI PMID:19734452 732180 Polg polymerase (DNA directed), gamma gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:15164064 732180 Polg polymerase (DNA directed), gamma gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16020738 732180 Polg polymerase (DNA directed), gamma gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20201001 MGI PMID:23418460 732180 Polg polymerase (DNA directed), gamma gene MP:0013659 abnormal erythroid lineage cell morphology IAGP N RGD:5509061 20150611 MGI PMID:19734452 732183 Trpm8 transient receptor potential cation channel, subfamily M, member 8 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:17481392 732183 Trpm8 transient receptor potential cation channel, subfamily M, member 8 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:17481391 732183 Trpm8 transient receptor potential cation channel, subfamily M, member 8 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:17481392 732183 Trpm8 transient receptor potential cation channel, subfamily M, member 8 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:17538622 732183 Trpm8 transient receptor potential cation channel, subfamily M, member 8 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:17481391 732183 Trpm8 transient receptor potential cation channel, subfamily M, member 8 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:17481392 732183 Trpm8 transient receptor potential cation channel, subfamily M, member 8 gene MP:0003663 abnormal thermosensation IAGP N RGD:5509061 20141003 MGI PMID:17481391 732183 Trpm8 transient receptor potential cation channel, subfamily M, member 8 gene MP:0003663 abnormal thermosensation IAGP N RGD:5509061 20141003 MGI PMID:17481392 732183 Trpm8 transient receptor potential cation channel, subfamily M, member 8 gene MP:0003663 abnormal thermosensation IAGP N RGD:5509061 20141003 MGI PMID:17538622 732183 Trpm8 transient receptor potential cation channel, subfamily M, member 8 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:17481391 732183 Trpm8 transient receptor potential cation channel, subfamily M, member 8 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:17481392 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210128 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:8608598 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:12727921 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:12923053 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0000578 ulcerated autopod IAGP N RGD:5509061 20141003 MGI PMID:18806225 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:11371356 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20170105 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15537876 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:15919828 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11371356 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8608598 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:10865997 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15537876 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001523 impaired righting response IEA N RGD:5509061 20181227 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200430 MGI PMID:15919828 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001655 multifocal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:8608598 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11371356 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001828 abnormal T cell activation IEA N RGD:5509061 20111116 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:11371356 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:14670297 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18641358 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11371356 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20200423 MGI PMID:20386712 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20160505 MGI PMID:22264274 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11371356 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0002145 abnormal T cell differentiation IEA N RGD:5509061 20190606 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21553074 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:14670297 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8608597 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141030 MGI PMID:24413774 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:8608598 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:14670297 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16688530 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18493980 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0002493 increased IgG level IEA N RGD:5509061 20111116 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20210128 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:12727921 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:12223448 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:14617019 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20141003 MGI PMID:17475277 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12223448 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20200423 MGI PMID:20386712 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:11371356 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20200423 MGI PMID:20386712 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17475277 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12923053 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0004978 decreased B-1 B cell number IEA N RGD:5509061 20181004 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:12923053 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:12923053 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0005015 increased T cell number IEA N RGD:5509061 20190606 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20181004 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0005025 abnormal response to infection IEA N RGD:5509061 20141003 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0005040 abnormal MHC II cell surface expression on macrophages IAGP N RGD:5509061 20141003 MGI PMID:14670297 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:12370359 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0005079 decreased cytotoxic T cell cytolysis IEA N RGD:5509061 20190606 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0005466 abnormal T-helper 2 physiology IEA N RGD:5509061 20111116 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:12923053 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8608597 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14617019 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:17475277 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20181004 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12727921 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008076 abnormal CD4-positive T cell differentiation IEA N RGD:5509061 20190606 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181004 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20190606 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008083 decreased single-positive T cell number IEA N RGD:5509061 20181004 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17078933 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:12923053 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:18209032 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008567 decreased interferon-gamma secretion IEA N RGD:5509061 20111116 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:12370359 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:14670297 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:17475277 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:12370359 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:18493980 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:14670297 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141030 MGI PMID:24413774 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008791 decreased NK cell degranulation IEA N RGD:5509061 20111116 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008891 decreased hepatocyte apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17475277 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:10865997 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0009785 abnormal susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20151217 MGI PMID:24489749 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141030 MGI PMID:24413774 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20160505 MGI PMID:22264274 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:21076615 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0010537 tumor regression IAGP N RGD:5509061 20141003 MGI PMID:16618773 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12370359 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190606 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181004 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0010857 pulmonary necrosis IAGP N RGD:5509061 20200423 MGI PMID:20386712 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:12923053 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0010964 increased compact bone volume IAGP N RGD:5509061 20141003 MGI PMID:12923053 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0011076 increased macrophage nitric oxide production IAGP N RGD:5509061 20141003 MGI PMID:21636857 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8608598 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15537876 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0013434 abnormal CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20181004 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20190606 MGI 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:11163195 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:14670297 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:16688530 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:8608597 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:8608598 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:11390995 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:16688530 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0020940 increased susceptibility to Togaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:11390995 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:15919828 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:20386712 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:8608598 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:20386712 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0031053 pleuritis IAGP N RGD:5509061 20200618 MGI PMID:20386712 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0031054 bronchiolitis IAGP N RGD:5509061 20200618 MGI PMID:20386712 732185 Stat1 signal transducer and activator of transcription 1 gene MP:0031155 small intestine hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:15919828 732187 Renbp renin binding protein gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10809771 732189 Chst3 carbohydrate sulfotransferase 3 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 732189 Chst3 carbohydrate sulfotransferase 3 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20220407 MGI PMID:23118208 732189 Chst3 carbohydrate sulfotransferase 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20111116 MGI 732189 Chst3 carbohydrate sulfotransferase 3 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20150226 MGI PMID:23118208 732189 Chst3 carbohydrate sulfotransferase 3 gene MP:0003063 increased coping response IEA N RGD:5509061 20111116 MGI 732189 Chst3 carbohydrate sulfotransferase 3 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20150226 MGI PMID:23118208 732189 Chst3 carbohydrate sulfotransferase 3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11696535 732189 Chst3 carbohydrate sulfotransferase 3 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20150226 MGI PMID:23118208 732189 Chst3 carbohydrate sulfotransferase 3 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20150226 MGI PMID:23118208 732189 Chst3 carbohydrate sulfotransferase 3 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20150226 MGI PMID:23118208 732192 Fcnb ficolin B gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23150716 732192 Fcnb ficolin B gene MP:0009062 impaired lectin complement pathway IAGP N RGD:5509061 20141003 MGI PMID:23150716 732192 Fcnb ficolin B gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23150716 732194 Vps4a vacuolar protein sorting 4A gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20201015 MGI PMID:26720614 732194 Vps4a vacuolar protein sorting 4A gene MP:0000691 enlarged spleen IEA N RGD:5509061 20160811 MGI 732194 Vps4a vacuolar protein sorting 4A gene MP:0000745 tremors IEA N RGD:5509061 20201231 MGI 732194 Vps4a vacuolar protein sorting 4A gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 732194 Vps4a vacuolar protein sorting 4A gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 732194 Vps4a vacuolar protein sorting 4A gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 732194 Vps4a vacuolar protein sorting 4A gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 732194 Vps4a vacuolar protein sorting 4A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20160811 MGI 732194 Vps4a vacuolar protein sorting 4A gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20160811 MGI 732194 Vps4a vacuolar protein sorting 4A gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 732194 Vps4a vacuolar protein sorting 4A gene MP:0009908 protruding tongue IEA N RGD:5509061 20210520 MGI 732194 Vps4a vacuolar protein sorting 4A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732195 Kcns2 K+ voltage-gated channel, subfamily S, 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 732198 Crot carnitine O-octanoyltransferase gene MP:0001863 blood vessel inflammation IAGP N RGD:5509061 20221215 MGI PMID:33356393 732198 Crot carnitine O-octanoyltransferase gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20230601 MGI 732198 Crot carnitine O-octanoyltransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20221215 MGI PMID:33356393 732198 Crot carnitine O-octanoyltransferase gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20221215 MGI PMID:33356393 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17060448 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17488728 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17060448 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17488728 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220428 MGI 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17060448 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:17060448 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:17488728 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:17488728 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17488728 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:17488728 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:17060448 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:17060448 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:17060448 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:17060448 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17488728 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20240523 MGI 732201 Abca2 ATP-binding cassette, sub-family A member 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:17060448 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12805272 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:2919115 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:8461026 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:2919115 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0001423 abnormal liquid preference IAGP N RGD:5509061 20141003 MGI PMID:14592933 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0001432 abnormal food preference IAGP N RGD:5509061 20141003 MGI PMID:14592933 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12805272 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20562441 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8461026 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:2919115 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0003978 decreased circulating carnitine level IAGP N RGD:5509061 20141003 MGI PMID:2919115 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0010028 aciduria IAGP N RGD:5509061 20141003 MGI PMID:8461026 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0010953 abnormal fatty acid oxidation IAGP N RGD:5509061 20141003 MGI PMID:2919115 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0011019 abnormal adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:9802886 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0011765 oroticaciduria IAGP N RGD:5509061 20141003 MGI PMID:8461026 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0030612 organic aciduria IAGP N RGD:5509061 20180906 MGI PMID:2712823 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0030612 organic aciduria IAGP N RGD:5509061 20180906 MGI PMID:2919115 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0030612 organic aciduria IAGP N RGD:5509061 20180906 MGI PMID:8461026 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0030615 ethylmalonic aciduria IAGP N RGD:5509061 20180906 MGI PMID:2712823 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0030615 ethylmalonic aciduria IAGP N RGD:5509061 20180906 MGI PMID:8461026 732203 Acads acyl-Coenzyme A dehydrogenase, short chain gene MP:0030656 decreased circulating glycine level IAGP N RGD:5509061 20180913 MGI PMID:2919115 732205 Csad cysteine sulfinic acid decarboxylase gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20160218 MGI PMID:24639894 732207 Myo7a myosin VIIA gene MP:0000032 cochlear degeneration IAGP N RGD:5509061 20200507 MGI PMID:31824252 732207 Myo7a myosin VIIA gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20160929 MGI PMID:27534441 732207 Myo7a myosin VIIA gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:6627025 732207 Myo7a myosin VIIA gene MP:0000045 abnormal hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9680294 732207 Myo7a myosin VIIA gene MP:0000436 abnormal head movements IEA N RGD:5509061 20141003 MGI 732207 Myo7a myosin VIIA gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21447681 732207 Myo7a myosin VIIA gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 732207 Myo7a myosin VIIA gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20150108 MGI 732207 Myo7a myosin VIIA gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20111116 MGI 732207 Myo7a myosin VIIA gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:15389316 732207 Myo7a myosin VIIA gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:16235133 732207 Myo7a myosin VIIA gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:17329413 732207 Myo7a myosin VIIA gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:22381527 732207 Myo7a myosin VIIA gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15389316 732207 Myo7a myosin VIIA gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200507 MGI PMID:31824252 732207 Myo7a myosin VIIA gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 732207 Myo7a myosin VIIA gene MP:0001408 stereotypic behavior IEA N RGD:5509061 20170105 MGI 732207 Myo7a myosin VIIA gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:15389316 732207 Myo7a myosin VIIA gene MP:0001411 spinning IAGP N RGD:5509061 20200507 MGI PMID:31824252 732207 Myo7a myosin VIIA gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17329413 732207 Myo7a myosin VIIA gene MP:0001512 trunk curl IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:13336002 732207 Myo7a myosin VIIA gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:16235133 732207 Myo7a myosin VIIA gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:17329413 732207 Myo7a myosin VIIA gene MP:0001523 impaired righting response IEA N RGD:5509061 20170105 MGI 732207 Myo7a myosin VIIA gene MP:0001525 impaired balance IEA N RGD:5509061 20111116 MGI 732207 Myo7a myosin VIIA gene MP:0001922 reduced male fertility IEA N RGD:5509061 20111116 MGI 732207 Myo7a myosin VIIA gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 732207 Myo7a myosin VIIA gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:9680294 732207 Myo7a myosin VIIA gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:13336002 732207 Myo7a myosin VIIA gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:14198707 732207 Myo7a myosin VIIA gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15389316 732207 Myo7a myosin VIIA gene MP:0001967 deafness IAGP N RGD:5509061 20160929 MGI PMID:27534441 732207 Myo7a myosin VIIA gene MP:0001967 deafness IAGP N RGD:5509061 20200507 MGI PMID:31824252 732207 Myo7a myosin VIIA gene MP:0002068 abnormal parental behavior IEA N RGD:5509061 20111116 MGI 732207 Myo7a myosin VIIA gene MP:0002183 gliosis IEA N RGD:5509061 20111116 MGI 732207 Myo7a myosin VIIA gene MP:0002622 abnormal cochlear hair cell morphology IEA N RGD:5509061 20111116 MGI 732207 Myo7a myosin VIIA gene MP:0002730 head shaking IEA N RGD:5509061 20111116 MGI 732207 Myo7a myosin VIIA gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:13336002 732207 Myo7a myosin VIIA gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:14198707 732207 Myo7a myosin VIIA gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:6627025 732207 Myo7a myosin VIIA gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20200507 MGI PMID:31824252 732207 Myo7a myosin VIIA gene MP:0003382 straub tail IEA N RGD:5509061 20141003 MGI 732207 Myo7a myosin VIIA gene MP:0003878 abnormal ear physiology IAGP N RGD:5509061 20141003 MGI PMID:14198707 732207 Myo7a myosin VIIA gene MP:0004331 vestibular saccular macula degeneration IAGP N RGD:5509061 20141003 MGI PMID:13336002 732207 Myo7a myosin VIIA gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:13336002 732207 Myo7a myosin VIIA gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:14198707 732207 Myo7a myosin VIIA gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15389316 732207 Myo7a myosin VIIA gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20200507 MGI PMID:31824252 732207 Myo7a myosin VIIA gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20141003 MGI PMID:14198707 732207 Myo7a myosin VIIA gene MP:0004364 thin stria vascularis IAGP N RGD:5509061 20200507 MGI PMID:31824252 732207 Myo7a myosin VIIA gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20332152 732207 Myo7a myosin VIIA gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:14648237 732207 Myo7a myosin VIIA gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18339676 732207 Myo7a myosin VIIA gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20200507 MGI PMID:31824252 732207 Myo7a myosin VIIA gene MP:0004413 absent cochlear microphonics IAGP N RGD:5509061 20141003 MGI PMID:9435277 732207 Myo7a myosin VIIA gene MP:0004415 abnormal cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:14648237 732207 Myo7a myosin VIIA gene MP:0004466 short cochlear outer hair cells IAGP N RGD:5509061 20141003 MGI PMID:18339676 732207 Myo7a myosin VIIA gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15389316 732207 Myo7a myosin VIIA gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20151001 MGI PMID:22381527 732207 Myo7a myosin VIIA gene MP:0004517 decreased vestibular hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:18160714 732207 Myo7a myosin VIIA gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:20016096 732207 Myo7a myosin VIIA gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:22381527 732207 Myo7a myosin VIIA gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:9435277 732207 Myo7a myosin VIIA gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:18339676 732207 Myo7a myosin VIIA gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:9435277 732207 Myo7a myosin VIIA gene MP:0004524 short cochlear hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:20016096 732207 Myo7a myosin VIIA gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:12121736 732207 Myo7a myosin VIIA gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:14648237 732207 Myo7a myosin VIIA gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15389316 732207 Myo7a myosin VIIA gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 732207 Myo7a myosin VIIA gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:20332152 732207 Myo7a myosin VIIA gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:14648237 732207 Myo7a myosin VIIA gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:15389316 732207 Myo7a myosin VIIA gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15389316 732207 Myo7a myosin VIIA gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 732207 Myo7a myosin VIIA gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:15389316 732207 Myo7a myosin VIIA gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:15389316 732207 Myo7a myosin VIIA gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0004577 abnormal cochlear hair cell inter-stereocilial links morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 732207 Myo7a myosin VIIA gene MP:0004582 absent cochlear hair bundle ankle links IAGP N RGD:5509061 20141003 MGI PMID:18339676 732207 Myo7a myosin VIIA gene MP:0004598 abnormal cochlear basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0004632 abnormal cochlear OHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:6627025 732207 Myo7a myosin VIIA gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:20016096 732207 Myo7a myosin VIIA gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20200507 MGI PMID:31824252 732207 Myo7a myosin VIIA gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12121736 732207 Myo7a myosin VIIA gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:14648237 732207 Myo7a myosin VIIA gene MP:0004767 increased cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:15389316 732207 Myo7a myosin VIIA gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 732207 Myo7a myosin VIIA gene MP:0004924 abnormal behavior IEA N RGD:5509061 20111116 MGI 732207 Myo7a myosin VIIA gene MP:0005191 head tilt IAGP N RGD:5509061 20200507 MGI PMID:31824252 732207 Myo7a myosin VIIA gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20016096 732207 Myo7a myosin VIIA gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:15389316 732207 Myo7a myosin VIIA gene MP:0005424 jerky movement IEA N RGD:5509061 20111116 MGI 732207 Myo7a myosin VIIA gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:14609561 732207 Myo7a myosin VIIA gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20150108 MGI 732207 Myo7a myosin VIIA gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 732207 Myo7a myosin VIIA gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20200507 MGI PMID:31824252 732207 Myo7a myosin VIIA gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:14648237 732207 Myo7a myosin VIIA gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:22381527 732207 Myo7a myosin VIIA gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:12121736 732207 Myo7a myosin VIIA gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:14198707 732207 Myo7a myosin VIIA gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:22381527 732207 Myo7a myosin VIIA gene MP:0006388 abnormal auditory summating potential IAGP N RGD:5509061 20141003 MGI PMID:9435277 732207 Myo7a myosin VIIA gene MP:0006409 vestibular ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:13336002 732207 Myo7a myosin VIIA gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21447681 732207 Myo7a myosin VIIA gene MP:0008489 slow postnatal weight gain IEA N RGD:5509061 20111116 MGI 732207 Myo7a myosin VIIA gene MP:0010323 retropulsion IEA N RGD:5509061 20111116 MGI 732207 Myo7a myosin VIIA gene MP:0011939 increased food intake IEA N RGD:5509061 20141003 MGI 732207 Myo7a myosin VIIA gene MP:0011941 increased fluid intake IEA N RGD:5509061 20141003 MGI 732207 Myo7a myosin VIIA gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17329413 732207 Myo7a myosin VIIA gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:22381527 732207 Myo7a myosin VIIA gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23251483 732207 Myo7a myosin VIIA gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20200507 MGI PMID:31824252 732207 Myo7a myosin VIIA gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200507 MGI PMID:31824252 732207 Myo7a myosin VIIA gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200507 MGI PMID:31824252 732207 Myo7a myosin VIIA gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200507 MGI PMID:31824252 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:17767909 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201022 MGI 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20201022 MGI 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17767909 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17767909 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17767909 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200116 MGI PMID:30820446 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200116 MGI PMID:30820446 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17767909 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:30820446 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20200116 MGI PMID:30820446 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200116 MGI PMID:30820446 732212 Kcnb1 potassium voltage gated channel, Shab-related subfamily, member 1 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200116 MGI PMID:30820446 732213 Cyp8b1 cytochrome P450, family 8, subfamily b, polypeptide 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:12393855 732213 Cyp8b1 cytochrome P450, family 8, subfamily b, polypeptide 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:15994119 732213 Cyp8b1 cytochrome P450, family 8, subfamily b, polypeptide 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12393855 732213 Cyp8b1 cytochrome P450, family 8, subfamily b, polypeptide 1 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:12393855 732213 Cyp8b1 cytochrome P450, family 8, subfamily b, polypeptide 1 gene MP:0002791 steatorrhea IAGP N RGD:5509061 20141003 MGI PMID:12393855 732213 Cyp8b1 cytochrome P450, family 8, subfamily b, polypeptide 1 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20141003 MGI PMID:12393855 732213 Cyp8b1 cytochrome P450, family 8, subfamily b, polypeptide 1 gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:12393855 732213 Cyp8b1 cytochrome P450, family 8, subfamily b, polypeptide 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15994119 732213 Cyp8b1 cytochrome P450, family 8, subfamily b, polypeptide 1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12393855 732213 Cyp8b1 cytochrome P450, family 8, subfamily b, polypeptide 1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15994119 732215 Vegfc vascular endothelial growth factor C gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18519586 732215 Vegfc vascular endothelial growth factor C gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18519586 732215 Vegfc vascular endothelial growth factor C gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:14634646 732215 Vegfc vascular endothelial growth factor C gene MP:0003390 lymphedema IAGP N RGD:5509061 20141003 MGI PMID:14634646 732215 Vegfc vascular endothelial growth factor C gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20141003 MGI PMID:14634646 732215 Vegfc vascular endothelial growth factor C gene MP:0004106 lymphatic vessel hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18519586 732215 Vegfc vascular endothelial growth factor C gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18519586 732215 Vegfc vascular endothelial growth factor C gene MP:0010194 absent lymphatic vessels IAGP N RGD:5509061 20141003 MGI PMID:14634646 732215 Vegfc vascular endothelial growth factor C gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14634646 732215 Vegfc vascular endothelial growth factor C gene MP:0012080 chylous ascites IAGP N RGD:5509061 20141003 MGI PMID:14634646 732215 Vegfc vascular endothelial growth factor C gene MP:0031440 lymphatic vessel hypoplasia IAGP N RGD:5509061 20220915 MGI PMID:14634646 732215 Vegfc vascular endothelial growth factor C gene MP:0031440 lymphatic vessel hypoplasia IAGP N RGD:5509061 20220915 MGI PMID:18519586 732216 Syt3 synaptotagmin III gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:15703192 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:15703192 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:15703192 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15703192 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15703192 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15703192 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15703192 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20201022 MGI 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20201022 MGI 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:15703192 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15703192 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20201022 MGI 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:15703192 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:15703192 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210826 MGI 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15703192 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0009908 protruding tongue IEA N RGD:5509061 20210520 MGI 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732218 Slc26a2 solute carrier family 26 (sulfate transporter), member 2 gene MP:0030223 mandibular hyperostosis IAGP N RGD:5509061 20171207 MGI PMID:15703192 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:14699507 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:14699507 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:16614371 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14699507 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20230330 MGI PMID:23180829 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20230330 MGI PMID:23180829 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0001926 female infertility IAGP N RGD:5509061 20230330 MGI PMID:23180829 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16614371 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0002645 abnormal intestinal cholesterol absorption IAGP N RGD:5509061 20150101 MGI PMID:25378657 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16614371 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20150101 MGI PMID:25378657 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20150101 MGI PMID:25378657 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20150101 MGI PMID:25378657 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14699507 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20150101 MGI PMID:25378657 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14699507 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20150101 MGI PMID:25378657 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20141003 MGI PMID:16614371 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:14699507 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14699507 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20150101 MGI PMID:25378657 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:14699507 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16614371 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20230330 MGI PMID:23180829 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0010074 stomatocytosis IAGP N RGD:5509061 20141003 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0010076 abnormal phytosterol level IAGP N RGD:5509061 20150101 MGI PMID:25378657 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0010077 increased phytosterol level IAGP N RGD:5509061 20150101 MGI PMID:25378657 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0010078 increased circulating phytosterol level IAGP N RGD:5509061 20141003 MGI PMID:14699507 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0010078 increased circulating phytosterol level IAGP N RGD:5509061 20150101 MGI PMID:25378657 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0013437 decreased phytosterol level IAGP N RGD:5509061 20150101 MGI PMID:25378657 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0013756 increased intestinal phytosterol absorption IAGP N RGD:5509061 20200102 MGI PMID:25378657 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0014060 abnormal platelet alpha-granule morphology IAGP N RGD:5509061 20170803 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0030025 giant platelets IAGP N RGD:5509061 20170803 MGI PMID:19846887 732220 Abcg5 ATP binding cassette subfamily G member 5 gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:19846887 732222 Gsr glutathione reductase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 732222 Gsr glutathione reductase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 732222 Gsr glutathione reductase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 732222 Gsr glutathione reductase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 732222 Gsr glutathione reductase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10218442 732222 Gsr glutathione reductase gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20111116 MGI 732222 Gsr glutathione reductase gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 732224 Cdipt CDP-diacylglycerol--inositol 3-phosphatidyltransferase gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 732224 Cdipt CDP-diacylglycerol--inositol 3-phosphatidyltransferase gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 732224 Cdipt CDP-diacylglycerol--inositol 3-phosphatidyltransferase gene MP:0011972 decreased circulating lactate dehydrogenase level IEA N RGD:5509061 20210128 MGI 732224 Cdipt CDP-diacylglycerol--inositol 3-phosphatidyltransferase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 732229 Cib1 calcium and integrin binding 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 732229 Cib1 calcium and integrin binding 1 gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20210128 MGI 732229 Cib1 calcium and integrin binding 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16982698 732229 Cib1 calcium and integrin binding 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16982698 732229 Cib1 calcium and integrin binding 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16982698 732229 Cib1 calcium and integrin binding 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210128 MGI 732229 Cib1 calcium and integrin binding 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16982698 732229 Cib1 calcium and integrin binding 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16982698 732229 Cib1 calcium and integrin binding 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20211021 MGI 732229 Cib1 calcium and integrin binding 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16982698 732229 Cib1 calcium and integrin binding 1 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20210128 MGI 732229 Cib1 calcium and integrin binding 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:16982698 732229 Cib1 calcium and integrin binding 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 732229 Cib1 calcium and integrin binding 1 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20210128 MGI 732232 Cntn1 contactin 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22242131 732232 Cntn1 contactin 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22242131 732232 Cntn1 contactin 1 gene MP:0001394 circling IEA N RGD:5509061 20150730 MGI 732232 Cntn1 contactin 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:22242131 732232 Cntn1 contactin 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0002183 gliosis IEA N RGD:5509061 20150730 MGI 732232 Cntn1 contactin 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0004263 abnormal limb posture IEA N RGD:5509061 20150730 MGI 732232 Cntn1 contactin 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0009512 abnormal cerebellar Golgi cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22242131 732232 Cntn1 contactin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10595523 732232 Cntn1 contactin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20150730 MGI 732232 Cntn1 contactin 1 gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20150730 MGI 732232 Cntn1 contactin 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22242131 732232 Cntn1 contactin 1 gene MP:0014085 stomach non-glandular epithelium hyperkeratosis IEA N RGD:5509061 20160310 MGI 732232 Cntn1 contactin 1 gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:10595523 732235 Lman1 lectin, mannose-binding, 1 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20150101 MGI PMID:24719406 732235 Lman1 lectin, mannose-binding, 1 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20180906 MGI PMID:29735583 732235 Lman1 lectin, mannose-binding, 1 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20180906 MGI PMID:29735583 732235 Lman1 lectin, mannose-binding, 1 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20180906 MGI PMID:29735583 732235 Lman1 lectin, mannose-binding, 1 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:21795745 732235 Lman1 lectin, mannose-binding, 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20150101 MGI PMID:24719406 732235 Lman1 lectin, mannose-binding, 1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20180906 MGI PMID:29735583 732235 Lman1 lectin, mannose-binding, 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21795745 732235 Lman1 lectin, mannose-binding, 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21795745 732235 Lman1 lectin, mannose-binding, 1 gene MP:0012328 decreased circulating factor VIII level IAGP N RGD:5509061 20180906 MGI PMID:29735583 732237 Tec tec protein tyrosine kinase gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11104803 732237 Tec tec protein tyrosine kinase gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:11104803 732237 Tec tec protein tyrosine kinase gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11104803 732237 Tec tec protein tyrosine kinase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11104803 732237 Tec tec protein tyrosine kinase gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:11104803 732237 Tec tec protein tyrosine kinase gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:11104803 732237 Tec tec protein tyrosine kinase gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11104803 732237 Tec tec protein tyrosine kinase gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11104803 732237 Tec tec protein tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11104803 732237 Tec tec protein tyrosine kinase gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11104803 732237 Tec tec protein tyrosine kinase gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:12842985 732237 Tec tec protein tyrosine kinase gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:11104803 732237 Tec tec protein tyrosine kinase gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11104803 732237 Tec tec protein tyrosine kinase gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:12842985 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230817 MGI PMID:37456838 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20230817 MGI PMID:37456838 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230817 MGI PMID:37456838 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230817 MGI PMID:37456838 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20230817 MGI PMID:37456838 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20230817 MGI PMID:37456838 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20230817 MGI PMID:37456838 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20230817 MGI PMID:37456838 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 732238 Kpna2 karyopherin subunit alpha 2 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20230817 MGI PMID:37456838 732239 Rest RE1-silencing transcription factor gene MP:0000373 belly spot IAGP N RGD:5509061 20181122 MGI PMID:25818501 732239 Rest RE1-silencing transcription factor gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:23022299 732239 Rest RE1-silencing transcription factor gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:9771705 732239 Rest RE1-silencing transcription factor gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:20969844 732239 Rest RE1-silencing transcription factor gene MP:0001525 impaired balance IAGP N RGD:5509061 20191212 MGI PMID:29961578 732239 Rest RE1-silencing transcription factor gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:9771705 732239 Rest RE1-silencing transcription factor gene MP:0001967 deafness IAGP N RGD:5509061 20191212 MGI PMID:29961578 732239 Rest RE1-silencing transcription factor gene MP:0002939 head spot IAGP N RGD:5509061 20181122 MGI PMID:25818501 732239 Rest RE1-silencing transcription factor gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:20969844 732239 Rest RE1-silencing transcription factor gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21396985 732239 Rest RE1-silencing transcription factor gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:21715642 732239 Rest RE1-silencing transcription factor gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:9771705 732239 Rest RE1-silencing transcription factor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9771705 732239 Rest RE1-silencing transcription factor gene MP:0004203 abnormal cranial flexure morphology IAGP N RGD:5509061 20141003 MGI PMID:23022299 732239 Rest RE1-silencing transcription factor gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20191212 MGI PMID:29961578 732239 Rest RE1-silencing transcription factor gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20191212 MGI PMID:29961578 732239 Rest RE1-silencing transcription factor gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20191212 MGI PMID:29961578 732239 Rest RE1-silencing transcription factor gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 732239 Rest RE1-silencing transcription factor gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20969844 732239 Rest RE1-silencing transcription factor gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210128 MGI 732239 Rest RE1-silencing transcription factor gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20969844 732239 Rest RE1-silencing transcription factor gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20191212 MGI PMID:29961578 732239 Rest RE1-silencing transcription factor gene MP:0006325 impaired hearing IAGP N RGD:5509061 20191212 MGI PMID:29961578 732239 Rest RE1-silencing transcription factor gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:23022299 732239 Rest RE1-silencing transcription factor gene MP:0008508 thick retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:20969844 732239 Rest RE1-silencing transcription factor gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20211021 MGI 732239 Rest RE1-silencing transcription factor gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21715642 732239 Rest RE1-silencing transcription factor gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:20969844 732239 Rest RE1-silencing transcription factor gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20181122 MGI PMID:25818501 732239 Rest RE1-silencing transcription factor gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21715642 732239 Rest RE1-silencing transcription factor gene MP:0011060 abnormal kinocilium morphology IAGP N RGD:5509061 20191212 MGI PMID:29961578 732239 Rest RE1-silencing transcription factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20181122 MGI PMID:25818501 732239 Rest RE1-silencing transcription factor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21715642 732239 Rest RE1-silencing transcription factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23022299 732239 Rest RE1-silencing transcription factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9771705 732239 Rest RE1-silencing transcription factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732239 Rest RE1-silencing transcription factor gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20191212 MGI PMID:29961578 732239 Rest RE1-silencing transcription factor gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:9771705 732239 Rest RE1-silencing transcription factor gene MP:0014265 thick retina inner plexiform layer IAGP N RGD:5509061 20230706 MGI PMID:20969844 732239 Rest RE1-silencing transcription factor gene MP:0030935 increased primordial germ cell apoptosis IAGP N RGD:5509061 20190411 MGI PMID:23022299 732240 Banf1 BAF nuclear assembly factor 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20230601 MGI 732240 Banf1 BAF nuclear assembly factor 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20230601 MGI 732240 Banf1 BAF nuclear assembly factor 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240926 MGI 732240 Banf1 BAF nuclear assembly factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 732240 Banf1 BAF nuclear assembly factor 1 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240926 MGI 732249 Pde7b phosphodiesterase 7B gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 732250 Guca2b guanylate cyclase activator 2b gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:14561709 732250 Guca2b guanylate cyclase activator 2b gene MP:0004216 salt-resistant hypertension IAGP N RGD:5509061 20141003 MGI PMID:14561709 732250 Guca2b guanylate cyclase activator 2b gene MP:0005556 abnormal renal filtration rate IAGP N RGD:5509061 20141003 MGI PMID:14561709 732250 Guca2b guanylate cyclase activator 2b gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:14561709 732250 Guca2b guanylate cyclase activator 2b gene MP:0005633 increased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:14561709 732250 Guca2b guanylate cyclase activator 2b gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:14561709 732250 Guca2b guanylate cyclase activator 2b gene MP:0008864 abnormal intestinal secretion IAGP N RGD:5509061 20141003 MGI PMID:14561709 732250 Guca2b guanylate cyclase activator 2b gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14561709 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20230601 MGI 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0000746 weakness IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0000833 thalamus hyperplasia IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:21423165 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:22699619 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24652766 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160630 MGI PMID:26886798 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170427 MGI PMID:26134648 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:21167025 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160630 MGI PMID:26886798 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20200723 MGI PMID:26559786 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20200723 MGI PMID:27492494 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:21423165 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21423165 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20160630 MGI PMID:26886798 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20191219 MGI PMID:31275112 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:24652766 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20200723 MGI PMID:27492494 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001394 circling IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:24652766 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190801 MGI PMID:27189882 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:24652766 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160630 MGI PMID:26886798 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170427 MGI PMID:26134648 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200723 MGI PMID:27492494 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20160630 MGI PMID:26886798 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20170427 MGI PMID:26134648 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:21423165 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20160630 MGI PMID:26886798 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20191219 MGI PMID:31275112 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20200723 MGI PMID:26559786 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20200723 MGI PMID:27492494 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20200723 MGI PMID:26559786 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21167025 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20200723 MGI PMID:26559786 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20200723 MGI PMID:27492494 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20191219 MGI PMID:31275112 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20170427 MGI PMID:26134648 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20170427 MGI PMID:26134648 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20200723 MGI PMID:26559786 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20200723 MGI PMID:27492494 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20190801 MGI PMID:27189882 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002083 premature death IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20161027 MGI PMID:25852484 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20170427 MGI PMID:26134648 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20191219 MGI PMID:31275112 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20210617 MGI PMID:30610205 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:24652766 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20161027 MGI PMID:25852484 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:21423165 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:24652766 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20160630 MGI PMID:26886798 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20200723 MGI PMID:27492494 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:24652766 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20200723 MGI PMID:26559786 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002801 abnormal long-term object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20170427 MGI PMID:26134648 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20200723 MGI PMID:27492494 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002806 abnormal conditioned emotional response IAGP N RGD:5509061 20141003 MGI PMID:24652766 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20191219 MGI PMID:31275112 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:21167025 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20161027 MGI PMID:25852484 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20170427 MGI PMID:26134648 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002917 decreased synaptic depression IEA N RGD:5509061 20141003 MGI 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002922 decreased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0002922 decreased post-tetanic potentiation IAGP N RGD:5509061 20170427 MGI PMID:26134648 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20161027 MGI PMID:25852484 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20200924 MGI PMID:30838762 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:24652766 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20170427 MGI PMID:26134648 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20200924 MGI PMID:30838762 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20200723 MGI PMID:26559786 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20200723 MGI PMID:27492494 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003908 decreased stereotypic behavior IAGP N RGD:5509061 20191219 MGI PMID:31275112 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:21423165 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21167025 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21423165 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20160630 MGI PMID:26886798 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20170427 MGI PMID:26134648 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20210617 MGI PMID:30610205 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21167025 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20191219 MGI PMID:31275112 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20191219 MGI PMID:31275112 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:24652766 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0008232 abnormal cingulum morphology IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20200723 MGI PMID:27492494 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21423165 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20160630 MGI PMID:26886798 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0008911 induced hyperactivity IEA N RGD:5509061 20141003 MGI 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:21423165 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0009455 enhanced cued conditioning behavior IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0009562 abnormal odor adaptation IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0009694 abnormal spinal cord commissure morphology IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:21558424 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20160630 MGI PMID:26886798 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0009944 abnormal olfactory lobe morphology IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0009976 abnormal cerebellar peduncle morphology IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:24652766 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0010540 long stride length IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24652766 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0011000 abnormal allogrooming behavior IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0011000 abnormal allogrooming behavior IAGP N RGD:5509061 20210617 MGI PMID:30610205 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20160630 MGI PMID:26687841 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20160630 MGI PMID:26886798 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0011622 abnormal habituation to a novel odor IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0012013 abnormal innate avoidance response IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0012296 impaired discrimination learning IAGP N RGD:5509061 20190801 MGI PMID:27189882 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20141003 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20161027 MGI PMID:25852484 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20170427 MGI PMID:26134648 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200723 MGI PMID:26559786 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200723 MGI PMID:27492494 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0012315 impaired learning IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0012480 decreased amygdala size IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0013140 excessive vocalization IAGP N RGD:5509061 20200723 MGI PMID:26559786 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0013787 photophobia IAGP N RGD:5509061 20150611 MGI PMID:24259569 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0014253 decreased paired-pulse ratio IAGP N RGD:5509061 20230706 MGI PMID:21167025 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0014381 abnormal miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:25852484 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:31275112 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:21167025 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161027 MGI PMID:27161151 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20210617 MGI PMID:30610205 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20200723 MGI PMID:27492494 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0020396 abnormal social recognition IAGP N RGD:5509061 20200723 MGI PMID:27492494 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20210617 MGI PMID:30610205 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0020512 abnormal dendritic mushroom spine morphology IAGP N RGD:5509061 20210617 MGI PMID:30610205 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0020514 abnormal dendritic thin spine morphology IAGP N RGD:5509061 20210617 MGI PMID:30610205 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20180301 MGI PMID:21423165 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20210617 MGI PMID:30610205 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0020864 premature suckling reflex loss IAGP N RGD:5509061 20200402 MGI PMID:30302388 732252 Shank3 SH3 and multiple ankyrin repeat domains 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:24652766 732254 S100a3 S100 calcium binding protein A3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 732254 S100a3 S100 calcium binding protein A3 gene MP:0001304 cataract IEA N RGD:5509061 20230601 MGI 732254 S100a3 S100 calcium binding protein A3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 732254 S100a3 S100 calcium binding protein A3 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230601 MGI 732254 S100a3 S100 calcium binding protein A3 gene MP:0002989 small kidney IEA N RGD:5509061 20230601 MGI 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9476659 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:8643592 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:9476659 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:8787763 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:9476659 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:12852850 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12852850 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8643592 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8787763 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9476659 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12852850 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:12852850 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0003697 absent zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:8643592 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0003697 absent zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:8787763 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0003697 absent zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:9476659 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:9476659 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0009372 abnormal cumulus oophorus morphology IAGP N RGD:5509061 20141003 MGI PMID:8643592 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0009375 thin zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:12852850 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0009375 thin zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:9107049 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:9476659 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:8643592 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:8787763 732255 Zp3 zona pellucida glycoprotein 3 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:9476659 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:12637252 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:10712348 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:8041705 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:23423996 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18949059 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18949059 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:10712348 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:23423996 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:8008068 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:10508270 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12637252 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:15503007 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:23423996 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:8008068 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:8144922 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:10712348 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8144922 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:23423996 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10508270 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18949059 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23423996 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:23423996 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:8008068 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:8008068 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:23423996 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:10508270 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20141003 MGI PMID:23423996 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23423996 732256 Fcer2a Fc receptor, IgE, low affinity II, alpha polypeptide gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10508270 732259 Cdc37 cell division cycle 37 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 732259 Cdc37 cell division cycle 37 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 732259 Cdc37 cell division cycle 37 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 732259 Cdc37 cell division cycle 37 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240919 MGI 732259 Cdc37 cell division cycle 37 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 732259 Cdc37 cell division cycle 37 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 732259 Cdc37 cell division cycle 37 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240919 MGI 732262 Rhd Rh blood group, D antigen gene MP:0001191 abnormal skin condition IEA N RGD:5509061 20160804 MGI 732262 Rhd Rh blood group, D antigen gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 732262 Rhd Rh blood group, D antigen gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20160804 MGI 732262 Rhd Rh blood group, D antigen gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 732262 Rhd Rh blood group, D antigen gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19807729 732262 Rhd Rh blood group, D antigen gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20160804 MGI 732262 Rhd Rh blood group, D antigen gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:19807729 732267 Enpep glutamyl aminopeptidase gene MP:0001488 increased startle reflex IEA N RGD:5509061 20181227 MGI 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0000161 scoliosis IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0000478 delayed intestine development IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:10559486 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10559486 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:10559486 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10230788 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10559486 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:10559486 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23349837 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12447443 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23349837 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:12756228 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:12756228 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:12756228 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:21317887 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:11157052 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002083 premature death IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:12756228 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12756228 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10230788 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:12756228 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12447443 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12447443 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:23349837 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:9851932 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:23349837 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16579967 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003153 early eyelid opening IAGP N RGD:5509061 20200123 MGI PMID:21862560 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16579967 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16043490 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:10559486 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003622 ischuria IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20200903 MGI PMID:31450635 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:12756228 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10559486 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:16579967 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11888903 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0004612 fusion of vertebral bodies IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0004685 calcified intervertebral disk IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:10230788 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11157052 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16579967 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12447443 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23349837 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16043490 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15567863 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9851932 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:23349837 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12447443 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16973441 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:12447443 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:23349837 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23349837 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0006257 abnormal fungiform papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0006392 abnormal nucleus pulposus morphology IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0006394 abnormal vertebral epiphyseal plate morphology IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11157052 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21317887 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9851932 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0008445 increased retina cone cell number IAGP N RGD:5509061 20200903 MGI PMID:31450635 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0008452 increased retina rod cell number IAGP N RGD:5509061 20200903 MGI PMID:31450635 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:10559486 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12447443 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15272135 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12447443 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23349837 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12447443 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0009603 absent keratohyalin granules IAGP N RGD:5509061 20170720 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12447443 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0010033 paraphimosis IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:23349837 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0010715 retina coloboma IAGP N RGD:5509061 20141003 MGI PMID:12756228 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10559486 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12756228 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15375216 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10230788 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10559486 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:16973441 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0011709 increased fibroblast cell migration IAGP N RGD:5509061 20150212 MGI PMID:16973441 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20170420 MGI PMID:23223452 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:23349837 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0012146 increased b-wave amplitude IAGP N RGD:5509061 20200903 MGI PMID:31450635 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0012194 decreased keratinocyte migration IAGP N RGD:5509061 20150212 MGI PMID:16973441 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10559486 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0012502 decreased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10230788 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0012502 decreased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10559486 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0012504 increased forebrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10230788 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0012504 increased forebrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10559486 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0012677 absent brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:10559486 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10230788 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0013176 abnormal tail position or orientation IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16973441 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17893331 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0030837 abnormal knee joint morphology IAGP N RGD:5509061 20220602 MGI PMID:30664861 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:20231445 732272 Mapk8 mitogen-activated protein kinase 8 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:20231445 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:8187759 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:8187759 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:8290590 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20220407 MGI PMID:17374637 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220331 MGI PMID:29386567 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8187759 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:8187759 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:8290590 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8187759 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8290590 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:8187759 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:8187759 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:8187759 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8187759 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8290590 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15509794 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17374637 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20220331 MGI PMID:29386567 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:15509794 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15509794 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17374637 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:8187759 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:8187759 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0002783 abnormal ovary secretion IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0003696 abnormal zona pellucida morphology IAGP N RGD:5509061 20141003 MGI PMID:15509794 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0003696 abnormal zona pellucida morphology IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:8290590 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8290590 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:8187759 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220331 MGI PMID:29386567 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:17374637 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8187759 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220331 MGI PMID:29386567 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0009375 thin zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:15509794 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20220811 MGI 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8187759 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8290590 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0011124 increased primary ovarian follicle number IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20170119 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0011952 decreased cardiac stroke volume IEA N RGD:5509061 20211021 MGI 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0012707 incomplete caudal neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:8290590 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0013176 abnormal tail position or orientation IAGP N RGD:5509061 20141003 MGI PMID:8187759 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220331 MGI PMID:29386567 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20200130 MGI PMID:21239444 732273 Mgat1 mannoside acetylglucosaminyltransferase 1 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:21239444 732276 Mid1 midline 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 732276 Mid1 midline 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 732276 Mid1 midline 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:24194544 732276 Mid1 midline 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:12444108 732276 Mid1 midline 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:12444108 732276 Mid1 midline 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 732276 Mid1 midline 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12444108 732276 Mid1 midline 1 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20230119 MGI 732276 Mid1 midline 1 gene MP:0002989 small kidney IEA N RGD:5509061 20230119 MGI 732276 Mid1 midline 1 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20230119 MGI 732276 Mid1 midline 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12444108 732276 Mid1 midline 1 gene MP:0004096 abnormal midbrain-hindbrain boundary development IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:24194544 732276 Mid1 midline 1 gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230119 MGI 732276 Mid1 midline 1 gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0009964 abnormal cerebellum lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0009988 abnormal cerebellum vermis lobule I morphology IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0009989 abnormal cerebellum vermis lobule II morphology IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0009990 abnormal cerebellum vermis lobule III morphology IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230119 MGI 732276 Mid1 midline 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12444108 732276 Mid1 midline 1 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:20181585 732276 Mid1 midline 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 732279 Ech1 enoyl coenzyme A hydratase 1, peroxisomal gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 732279 Ech1 enoyl coenzyme A hydratase 1, peroxisomal gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:15517609 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:16275892 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9166425 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:9329966 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:15593301 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11875005 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15557190 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15557190 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:9166425 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:9166425 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:10587518 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:10587518 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:16275892 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:10619859 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:10940928 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9166425 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:10587518 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:10587518 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17138939 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:9166425 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:10587518 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0005614 decreased susceptibility to type III hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:15517609 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10587518 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15593301 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15593301 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19603542 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:10587518 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:10587518 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15557190 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15557190 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:9329966 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10587518 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17138939 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:15557190 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:15557190 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:15557190 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:15593301 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:9329966 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15557190 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20141003 MGI PMID:11875005 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15557190 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:16275892 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:15557190 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0011076 increased macrophage nitric oxide production IAGP N RGD:5509061 20141003 MGI PMID:15557190 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:10587518 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:15593301 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:19079579 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:19079579 732280 Ccr1 C-C motif chemokine receptor 1 gene MP:0031054 bronchiolitis IAGP N RGD:5509061 20200709 MGI PMID:19079579 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12169661 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:15591354 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20230601 MGI 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:15591354 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15591354 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:12169661 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:12169661 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:12169661 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12169661 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12169661 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15591354 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20230601 MGI 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:12169661 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15591354 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17947234 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20230601 MGI 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17947234 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:12169661 732281 Nherf1 NHERF family PDZ scaffold protein 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12169661 732282 Alas2 aminolevulinic acid synthase 2, erythroid gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10562540 732282 Alas2 aminolevulinic acid synthase 2, erythroid gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:10562540 732282 Alas2 aminolevulinic acid synthase 2, erythroid gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10562540 732282 Alas2 aminolevulinic acid synthase 2, erythroid gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:10562540 732282 Alas2 aminolevulinic acid synthase 2, erythroid gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:10562540 732282 Alas2 aminolevulinic acid synthase 2, erythroid gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:10562540 732282 Alas2 aminolevulinic acid synthase 2, erythroid gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10562540 732284 Cplx2 complexin 2 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20412316 732284 Cplx2 complexin 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20412316 732284 Cplx2 complexin 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0001440 abnormal grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0001446 abnormal whisker trimming behavior IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:20412316 732284 Cplx2 complexin 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10383625 732284 Cplx2 complexin 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11128041 732284 Cplx2 complexin 2 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:20412316 732284 Cplx2 complexin 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20412316 732284 Cplx2 complexin 2 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:18505837 732284 Cplx2 complexin 2 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11163241 732284 Cplx2 complexin 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:20412316 732284 Cplx2 complexin 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18505837 732284 Cplx2 complexin 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18505837 732284 Cplx2 complexin 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18505837 732284 Cplx2 complexin 2 gene MP:0005357 novel environmental response-related retropulsion IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:18505837 732284 Cplx2 complexin 2 gene MP:0005507 tail dragging IAGP N RGD:5509061 20141003 MGI PMID:12915444 732284 Cplx2 complexin 2 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:20412316 732284 Cplx2 complexin 2 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20412316 732284 Cplx2 complexin 2 gene MP:0010746 abnormal pre-Botzinger complex physiology IAGP N RGD:5509061 20141003 MGI PMID:18505837 732284 Cplx2 complexin 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11163241 732284 Cplx2 complexin 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18505837 732284 Cplx2 complexin 2 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:18505837 732284 Cplx2 complexin 2 gene MP:0014372 decreased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:18505837 732284 Cplx2 complexin 2 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:18505837 732284 Cplx2 complexin 2 gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:18505837 732284 Cplx2 complexin 2 gene MP:0020083 decreased hippocampus volume IAGP N RGD:5509061 20170706 MGI PMID:20412316 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:19332558 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:18487195 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0004081 abnormal globus pallidus morphology IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0004081 abnormal globus pallidus morphology IAGP N RGD:5509061 20141003 MGI PMID:19332558 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:19332558 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:19332558 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:18487195 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0008129 absent brain internal capsule IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:18487195 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:18487195 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19332558 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0011881 distended duodenum IAGP N RGD:5509061 20141003 MGI PMID:15778712 732288 Celsr3 cadherin, EGF LAG seven-pass G-type receptor 3 gene MP:0012484 decreased corticospinal tract size IAGP N RGD:5509061 20141003 MGI PMID:15778712 732289 Clec10a C-type lectin domain family 10, member A gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20240509 MGI PMID:31811054 732289 Clec10a C-type lectin domain family 10, member A gene MP:0001194 dermatitis IAGP N RGD:5509061 20240509 MGI PMID:31811054 732289 Clec10a C-type lectin domain family 10, member A gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:12077344 732289 Clec10a C-type lectin domain family 10, member A gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12077344 732289 Clec10a C-type lectin domain family 10, member A gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12077344 732289 Clec10a C-type lectin domain family 10, member A gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:12077344 732289 Clec10a C-type lectin domain family 10, member A gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:12077344 732289 Clec10a C-type lectin domain family 10, member A gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:12077344 732289 Clec10a C-type lectin domain family 10, member A gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12077344 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000018 small ears IAGP N RGD:5509061 20161216 MGI PMID:21479780 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000018 small ears IAGP N RGD:5509061 20170928 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000022 abnormal ear shape IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000023 abnormal ear position IEA N RGD:5509061 20120126 MGI 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000040 absent middle ear ossicles IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:10942429 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20160915 MGI PMID:21538817 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230629 MGI PMID:19809474 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20221006 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:16120640 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:18832392 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20230629 MGI PMID:19809474 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15621532 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15621532 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18297725 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20150716 MGI PMID:25843682 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20150716 MGI PMID:25843682 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000380 small hair follicles IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20161216 MGI PMID:21479780 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000445 short snout IAGP N RGD:5509061 20161216 MGI PMID:21479780 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:18653563 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:15581874 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:16442091 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:21128305 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:15581874 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:16120640 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:16120640 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:10942429 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000648 absent sebaceous gland IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:16715082 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000798 abnormal frontal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:16715082 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12682014 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:12682014 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:12682014 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000865 absent cerebellum vermis IAGP N RGD:5509061 20141003 MGI PMID:12682014 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:12682014 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16772167 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001063 abnormal trochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12682014 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20150716 MGI PMID:25843682 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20150716 MGI PMID:25843682 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150716 MGI PMID:25843682 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10942429 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:10942429 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12682014 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12682014 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001426 polydipsia IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:12682014 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:18653563 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:16120640 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:12682014 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001874 acanthosis IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001874 acanthosis IAGP N RGD:5509061 20150716 MGI PMID:25843682 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20151112 MGI PMID:23358455 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20150716 MGI PMID:25843682 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20150716 MGI PMID:25843682 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12682014 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:10191046 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10191046 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10191046 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16120640 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10942429 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10191046 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002174 abnormal gastrulation movements IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002174 abnormal gastrulation movements IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:21479780 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16715082 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16715082 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20221006 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:15621532 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15621532 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18297725 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15621532 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15621532 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20150716 MGI PMID:25843682 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:16772167 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:15581874 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15621532 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20141003 MGI PMID:12682014 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003853 dry skin IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003854 abnormal forelimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:16120640 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:16120640 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003878 abnormal ear physiology IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:21479780 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21479780 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20141003 MGI PMID:16890158 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004301 absent organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004403 absent cochlear outer hair cells IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004408 decreased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004415 abnormal cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20171019 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:15581874 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004573 absent limb buds IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004574 broad limb buds IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004576 abnormal embryonic autopod plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16120640 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004589 abnormal cochlear hair cell development IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004617 sacral vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004648 decreased thoracic vertebrae number IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004651 increased thoracic vertebrae number IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004831 long incisors IAGP N RGD:5509061 20141003 MGI PMID:10942429 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18653563 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:15581874 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:16442091 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:21128305 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20150716 MGI PMID:25843682 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:10942429 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:21479780 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:21479780 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20221006 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:16120640 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20160915 MGI PMID:21538817 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20160915 MGI PMID:21538817 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16120640 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:16715082 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20170928 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:15581874 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:16442091 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:19386268 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0006338 abnormal second pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0008219 abnormal dorsal telencephalic commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16715082 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0008221 abnormal hippocampal commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16715082 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0008381 absent gonial bone IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20150716 MGI PMID:25843682 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:15621532 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:18832392 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0008854 bleb IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0008863 craniofacial asymmetry IAGP N RGD:5509061 20141003 MGI PMID:10942429 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0008970 choanal atresia IAGP N RGD:5509061 20230629 MGI PMID:19809474 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20150716 MGI PMID:25843682 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:12682014 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009039 absent inferior colliculus IAGP N RGD:5509061 20141003 MGI PMID:12682014 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20150716 MGI PMID:25843682 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20221006 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221006 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009744 postaxial polydactyly IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009845 abnormal neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221006 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221006 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009889 persistence of medial edge epithelium during palatal shelf fusion IAGP N RGD:5509061 20221006 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221006 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009893 cleft primary palate IAGP N RGD:5509061 20221006 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009897 decreased maxillary shelf size IAGP N RGD:5509061 20221006 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20221006 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009914 abnormal hyoid bone lesser horn morphology IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0010326 malleus hypoplasia IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20210128 MGI 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0010678 abnormal skin adnexa morphology IAGP N RGD:5509061 20150716 MGI PMID:20308431 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0010728 fusion of atlas and occipital bones IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0010979 small ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:16442091 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0010979 small ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:21128305 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0010980 ectopic ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:16442091 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0010980 ectopic ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:21128305 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0010982 abnormal ureteric bud elongation IAGP N RGD:5509061 20141003 MGI PMID:16442091 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:21128305 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:21128305 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16120640 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20230629 MGI PMID:19809474 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10191046 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11857785 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12194867 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12682014 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11857785 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21479780 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20230629 MGI PMID:19809474 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011208 small proamniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011256 abnormal neural fold morphology IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011256 abnormal neural fold morphology IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011257 abnormal head fold morphology IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16442091 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16442091 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21128305 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011387 absent metanephric mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:16442091 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16442091 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011485 abnormal urethra urothelium morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011696 absent mast cells IAGP N RGD:5509061 20150716 MGI PMID:25843682 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011772 genital tubercle hypoplasia IAGP N RGD:5509061 20151112 MGI PMID:23358455 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20141003 MGI 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10942429 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20160915 MGI PMID:21538817 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0012131 small visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:8001823 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0012183 decreased paraxial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0012183 decreased paraxial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0012183 decreased paraxial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:9694798 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0012274 increased axial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:16421190 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0012274 increased axial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0012556 increased cell death IAGP N RGD:5509061 20231221 MGI PMID:28483978 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0012683 absent telencephalon IAGP N RGD:5509061 20231221 MGI PMID:28483978 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0012740 abnormal posterior primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0013164 abnormal forelimb bud morphology IAGP N RGD:5509061 20150528 MGI PMID:16120640 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0013268 second pharyngeal arch hypoplasia IAGP N RGD:5509061 20170420 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0014051 abnormal maxillary-premaxillary suture morphology IAGP N RGD:5509061 20160915 MGI PMID:21538817 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:16120640 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0020515 abnormal visceral yolk sac endoderm morphology IAGP N RGD:5509061 20180125 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0020516 abnormal visceral yolk sac mesenchyme morphology IAGP N RGD:5509061 20180125 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030084 tympanic ring hypoplasia IAGP N RGD:5509061 20170928 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030099 facial asymmetry IAGP N RGD:5509061 20170928 MGI PMID:10942429 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030107 incus hypoplasia IAGP N RGD:5509061 20170928 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030108 abnormal incudostapedial joint morphology IAGP N RGD:5509061 20171207 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030119 abnormal retrotympanic process morphology IAGP N RGD:5509061 20171005 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030124 middle ear ossicle hypoplasia IAGP N RGD:5509061 20170928 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030125 small gonial bone IAGP N RGD:5509061 20170928 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030128 stapes hypoplasia IAGP N RGD:5509061 20170928 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030160 abnormal auditory bulla morphology IAGP N RGD:5509061 20171207 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030249 small frontonasal prominence IAGP N RGD:5509061 20221006 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030322 styloid process hypoplasia IAGP N RGD:5509061 20171109 MGI PMID:26341559 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171207 MGI PMID:10942429 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030354 premature sagittal suture closure IAGP N RGD:5509061 20171207 MGI PMID:10942429 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030367 premature metopic suture closure IAGP N RGD:5509061 20171207 MGI PMID:10942429 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030394 abnormal incus short process morphology IAGP N RGD:5509061 20171207 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030396 abnormal incus long process morphology IAGP N RGD:5509061 20171207 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030398 absent incus lenticular process IAGP N RGD:5509061 20171207 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030399 abnormal incus body morphology IAGP N RGD:5509061 20171207 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030403 absent stapes head IAGP N RGD:5509061 20171207 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030408 abnormal stapes posterior crus morphology IAGP N RGD:5509061 20171207 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030411 decreased round window size IAGP N RGD:5509061 20171207 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030412 absent round window IAGP N RGD:5509061 20171207 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030419 excessive cerumen IAGP N RGD:5509061 20171207 MGI PMID:15630379 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030434 premature maxillary-premaxillary suture closure IAGP N RGD:5509061 20171214 MGI PMID:21538817 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030438 increased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:10942429 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0030537 abnormal notochordal process morphology IAGP N RGD:5509061 20180201 MGI PMID:8001822 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:12514106 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:23754280 732291 Fgfr1 fibroblast growth factor receptor 1 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:23754280 732293 Chek1 checkpoint kinase 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15261141 732293 Chek1 checkpoint kinase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10859164 732293 Chek1 checkpoint kinase 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15261141 732293 Chek1 checkpoint kinase 1 gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:20473325 732293 Chek1 checkpoint kinase 1 gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20473325 732293 Chek1 checkpoint kinase 1 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:20473325 732293 Chek1 checkpoint kinase 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15261141 732293 Chek1 checkpoint kinase 1 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:15261141 732293 Chek1 checkpoint kinase 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10859164 732293 Chek1 checkpoint kinase 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20473325 732293 Chek1 checkpoint kinase 1 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20473325 732293 Chek1 checkpoint kinase 1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:10859163 732293 Chek1 checkpoint kinase 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:20473325 732293 Chek1 checkpoint kinase 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:10859164 732293 Chek1 checkpoint kinase 1 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:20473325 732293 Chek1 checkpoint kinase 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:20473325 732293 Chek1 checkpoint kinase 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:10859163 732293 Chek1 checkpoint kinase 1 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:10859164 732293 Chek1 checkpoint kinase 1 gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20181115 MGI PMID:23557358 732293 Chek1 checkpoint kinase 1 gene MP:0004966 abnormal inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:10859163 732293 Chek1 checkpoint kinase 1 gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20181115 MGI PMID:23557358 732293 Chek1 checkpoint kinase 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10859164 732293 Chek1 checkpoint kinase 1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:15261141 732293 Chek1 checkpoint kinase 1 gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20181115 MGI PMID:23557358 732293 Chek1 checkpoint kinase 1 gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20181115 MGI PMID:23557358 732293 Chek1 checkpoint kinase 1 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:20473325 732293 Chek1 checkpoint kinase 1 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20181115 MGI PMID:23557358 732293 Chek1 checkpoint kinase 1 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:20473325 732293 Chek1 checkpoint kinase 1 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20473325 732293 Chek1 checkpoint kinase 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10859164 732293 Chek1 checkpoint kinase 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10859163 732293 Chek1 checkpoint kinase 1 gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20181115 MGI PMID:23557358 732293 Chek1 checkpoint kinase 1 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:10859163 732293 Chek1 checkpoint kinase 1 gene MP:0012743 increased inner cell mass apoptosis IAGP N RGD:5509061 20181115 MGI PMID:10859163 732293 Chek1 checkpoint kinase 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150219 MGI PMID:10859164 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17098861 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:11087842 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11087842 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001140 abnormal vagina epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11087842 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17098861 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18690289 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11087842 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:14996752 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20170105 MGI 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11087842 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17098861 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14996752 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:14996752 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20170105 MGI 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18690289 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002332 abnormal exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:14996752 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:14996752 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:11087842 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:18690289 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17098861 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17349961 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11087842 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17098861 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17349961 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17349961 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:17349961 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:17349961 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:17349961 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17349961 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17349961 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:17098861 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17098861 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0009341 decreased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17349961 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17098861 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14996752 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14996752 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14996752 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:17349961 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:20534466 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10823921 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:14996752 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16675958 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:18957541 732296 Ncoa3 nuclear receptor coactivator 3 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:10823921 732299 Fbxo6 F-box protein 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210923 MGI PMID:34215698 732299 Fbxo6 F-box protein 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210923 MGI PMID:34215698 732299 Fbxo6 F-box protein 6 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20210923 MGI PMID:34215698 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12514127 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12514127 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21593326 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21903816 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12514127 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21593326 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21593326 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:21593326 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:12514127 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:21593326 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:21903816 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21903816 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21593326 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21903816 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12514127 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:21903816 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:12514127 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:21593326 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20141003 MGI PMID:12514127 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0003470 abnormal summary potential IAGP N RGD:5509061 20141003 MGI PMID:12514127 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0003488 decreased channel response intensity IAGP N RGD:5509061 20141003 MGI PMID:12514127 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21903816 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0005159 azoospermia IEA N RGD:5509061 20141003 MGI 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:21903816 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:12514127 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20180215 MGI 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21903816 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:19150498 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0011084 lethality at weaning, incomplete penetrance IEA N RGD:5509061 20141003 MGI 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20141003 MGI 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:21593326 732306 Hcn2 hyperpolarization-activated, cyclic nucleotide-gated K+ 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20141003 MGI 732309 Nox1 NADPH oxidase 1 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:16386251 732309 Nox1 NADPH oxidase 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16386251 732309 Nox1 NADPH oxidase 1 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:16246966 732309 Nox1 NADPH oxidase 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20151126 MGI PMID:23749776 732309 Nox1 NADPH oxidase 1 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:23241962 732309 Nox1 NADPH oxidase 1 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16246966 732309 Nox1 NADPH oxidase 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20151126 MGI PMID:23749776 732309 Nox1 NADPH oxidase 1 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20141003 MGI PMID:23241962 732309 Nox1 NADPH oxidase 1 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20151126 MGI PMID:23749776 732309 Nox1 NADPH oxidase 1 gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:23241962 732309 Nox1 NADPH oxidase 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:16386251 732309 Nox1 NADPH oxidase 1 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16386251 732309 Nox1 NADPH oxidase 1 gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20151126 MGI PMID:23749776 732311 Plpp1 phospholipid phosphatase 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19215222 732313 Insl3 insulin-like 3 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10319319 732313 Insl3 insulin-like 3 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10319319 732313 Insl3 insulin-like 3 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10391220 732313 Insl3 insulin-like 3 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:10391220 732313 Insl3 insulin-like 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10319319 732313 Insl3 insulin-like 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10391220 732313 Insl3 insulin-like 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10319319 732313 Insl3 insulin-like 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10391220 732313 Insl3 insulin-like 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10391220 732313 Insl3 insulin-like 3 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:10319319 732313 Insl3 insulin-like 3 gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10319319 732313 Insl3 insulin-like 3 gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:10319319 732313 Insl3 insulin-like 3 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:10319319 732313 Insl3 insulin-like 3 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:10391220 732313 Insl3 insulin-like 3 gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:10391220 732313 Insl3 insulin-like 3 gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:10319319 732313 Insl3 insulin-like 3 gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:10319319 732313 Insl3 insulin-like 3 gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20141003 MGI PMID:10319319 732313 Insl3 insulin-like 3 gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:10319319 732313 Insl3 insulin-like 3 gene MP:0005149 abnormal gubernaculum morphology IAGP N RGD:5509061 20141003 MGI PMID:10319319 732313 Insl3 insulin-like 3 gene MP:0005149 abnormal gubernaculum morphology IAGP N RGD:5509061 20141003 MGI PMID:10391220 732313 Insl3 insulin-like 3 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:10391220 732313 Insl3 insulin-like 3 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:10391220 732313 Insl3 insulin-like 3 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:10391220 732313 Insl3 insulin-like 3 gene MP:0031286 unilateral cryptorchism IAGP N RGD:5509061 20211014 MGI PMID:10391220 732313 Insl3 insulin-like 3 gene MP:0031287 bilateral cryptorchism IAGP N RGD:5509061 20211014 MGI PMID:10319319 732313 Insl3 insulin-like 3 gene MP:0031287 bilateral cryptorchism IAGP N RGD:5509061 20211014 MGI PMID:10391220 732315 Rps2 ribosomal protein S2 gene MP:0000746 weakness IAGP N RGD:5509061 20220310 MGI PMID:34103648 732315 Rps2 ribosomal protein S2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220310 MGI PMID:34103648 732315 Rps2 ribosomal protein S2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220310 MGI PMID:34103648 732315 Rps2 ribosomal protein S2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20220310 MGI PMID:34103648 732315 Rps2 ribosomal protein S2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20220310 MGI PMID:34103648 732315 Rps2 ribosomal protein S2 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20220310 MGI PMID:34103648 732315 Rps2 ribosomal protein S2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20220310 MGI PMID:34103648 732317 Nell2 NEL-like 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20201022 MGI PMID:32499443 732317 Nell2 NEL-like 2 gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20201022 MGI PMID:32499443 732317 Nell2 NEL-like 2 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:15094495 732317 Nell2 NEL-like 2 gene MP:0004935 epididymis degeneration IAGP N RGD:5509061 20230601 MGI PMID:37095084 732317 Nell2 NEL-like 2 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20201022 MGI PMID:32499443 732317 Nell2 NEL-like 2 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20201022 MGI PMID:32499443 732318 Cyb5a cytochrome b5 type A (microsomal) gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:18805792 732319 Cfi complement component factor i gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 732319 Cfi complement component factor i gene MP:0002472 impaired complement alternative pathway IAGP N RGD:5509061 20230727 MGI PMID:34149444 732319 Cfi complement component factor i gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 732319 Cfi complement component factor i gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20160421 MGI 732319 Cfi complement component factor i gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:18202746 732319 Cfi complement component factor i gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:18202746 732319 Cfi complement component factor i gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20201001 MGI PMID:18202746 732319 Cfi complement component factor i gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20230727 MGI PMID:34149444 732319 Cfi complement component factor i gene MP:0011566 abnormal complement protein level IAGP N RGD:5509061 20230727 MGI PMID:34149444 732319 Cfi complement component factor i gene MP:0020216 decreased circulating complement protein level IAGP N RGD:5509061 20201001 MGI PMID:18202746 732319 Cfi complement component factor i gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:18202746 732321 Serpind1 serine (or cysteine) peptidase inhibitor, clade D, member 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:17549254 732321 Serpind1 serine (or cysteine) peptidase inhibitor, clade D, member 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:17549254 732321 Serpind1 serine (or cysteine) peptidase inhibitor, clade D, member 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17549254 732321 Serpind1 serine (or cysteine) peptidase inhibitor, clade D, member 1 gene MP:0005489 vascular smooth muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17549254 732321 Serpind1 serine (or cysteine) peptidase inhibitor, clade D, member 1 gene MP:0009548 abnormal platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:17549254 732321 Serpind1 serine (or cysteine) peptidase inhibitor, clade D, member 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17549254 732321 Serpind1 serine (or cysteine) peptidase inhibitor, clade D, member 1 gene MP:0011477 abnormal urine nucleoside level IAGP N RGD:5509061 20141003 MGI PMID:17549254 732321 Serpind1 serine (or cysteine) peptidase inhibitor, clade D, member 1 gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:11805133 732321 Serpind1 serine (or cysteine) peptidase inhibitor, clade D, member 1 gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:17549254 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20220407 MGI PMID:34099816 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20220407 MGI PMID:34099816 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20220407 MGI PMID:34099816 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16222232 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22002768 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22002768 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:22002768 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22002768 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20220407 MGI PMID:34099816 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22002768 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:22002768 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22002768 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20220407 MGI PMID:34099816 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:16222232 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20220407 MGI PMID:34099816 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0005655 increased aggression IAGP N RGD:5509061 20220407 MGI PMID:34099816 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17074043 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20220407 MGI PMID:34099816 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0012293 impaired active avoidance behavior IAGP N RGD:5509061 20220407 MGI PMID:34099816 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0014372 decreased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:23522044 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0014372 decreased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:34099816 732323 Cacng8 calcium channel, voltage-dependent, gamma subunit 8 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20220407 MGI PMID:34099816 732326 Epb41l3 erythrocyte membrane protein band 4.1 like 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21966409 732326 Epb41l3 erythrocyte membrane protein band 4.1 like 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21966409 732326 Epb41l3 erythrocyte membrane protein band 4.1 like 3 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:21966409 732326 Epb41l3 erythrocyte membrane protein band 4.1 like 3 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:21966409 732326 Epb41l3 erythrocyte membrane protein band 4.1 like 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21966409 732326 Epb41l3 erythrocyte membrane protein band 4.1 like 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21632923 732326 Epb41l3 erythrocyte membrane protein band 4.1 like 3 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21966409 732326 Epb41l3 erythrocyte membrane protein band 4.1 like 3 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:21966409 732326 Epb41l3 erythrocyte membrane protein band 4.1 like 3 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141003 MGI PMID:21966409 732326 Epb41l3 erythrocyte membrane protein band 4.1 like 3 gene MP:0010734 abnormal paranode morphology IAGP N RGD:5509061 20141003 MGI PMID:21632923 732326 Epb41l3 erythrocyte membrane protein band 4.1 like 3 gene MP:0010735 abnormal paranodal axoglial junction morphology IAGP N RGD:5509061 20141003 MGI PMID:21632923 732326 Epb41l3 erythrocyte membrane protein band 4.1 like 3 gene MP:0010738 abnormal internode morphology IAGP N RGD:5509061 20141003 MGI PMID:21966409 732330 Fgf3 fibroblast growth factor 3 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0000041 absent endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:12810586 732330 Fgf3 fibroblast growth factor 3 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:20171206 732330 Fgf3 fibroblast growth factor 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:20171206 732330 Fgf3 fibroblast growth factor 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0000588 thick tail IAGP N RGD:5509061 20141003 MGI PMID:14623822 732330 Fgf3 fibroblast growth factor 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:12810586 732330 Fgf3 fibroblast growth factor 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:14623822 732330 Fgf3 fibroblast growth factor 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:20171206 732330 Fgf3 fibroblast growth factor 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0000592 short tail IAGP N RGD:5509061 20170511 MGI PMID:26666435 732330 Fgf3 fibroblast growth factor 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20190502 MGI 732330 Fgf3 fibroblast growth factor 3 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0001262 decreased body weight IEA N RGD:5509061 20190103 MGI 732330 Fgf3 fibroblast growth factor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170511 MGI PMID:26666435 732330 Fgf3 fibroblast growth factor 3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0001394 circling IAGP N RGD:5509061 20170511 MGI PMID:26666435 732330 Fgf3 fibroblast growth factor 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 732330 Fgf3 fibroblast growth factor 3 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 732330 Fgf3 fibroblast growth factor 3 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20170511 MGI PMID:26666435 732330 Fgf3 fibroblast growth factor 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20171206 732330 Fgf3 fibroblast growth factor 3 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 732330 Fgf3 fibroblast growth factor 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:20171206 732330 Fgf3 fibroblast growth factor 3 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:14623822 732330 Fgf3 fibroblast growth factor 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20171206 732330 Fgf3 fibroblast growth factor 3 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:12810586 732330 Fgf3 fibroblast growth factor 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0003165 absent superior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0003168 abnormal scala vestibuli morphology IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0003169 abnormal scala media morphology IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0003637 cochlear ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0003938 abnormal ear development IAGP N RGD:5509061 20141003 MGI PMID:14623822 732330 Fgf3 fibroblast growth factor 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0004309 absent otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:12810586 732330 Fgf3 fibroblast growth factor 3 gene MP:0004309 absent otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:20171206 732330 Fgf3 fibroblast growth factor 3 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:12810586 732330 Fgf3 fibroblast growth factor 3 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:14623822 732330 Fgf3 fibroblast growth factor 3 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:20171206 732330 Fgf3 fibroblast growth factor 3 gene MP:0004313 absent vestibulocochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:14623822 732330 Fgf3 fibroblast growth factor 3 gene MP:0004493 dilated cochlea IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0004923 absent common crus IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0005191 head tilt IAGP N RGD:5509061 20170511 MGI PMID:26666435 732330 Fgf3 fibroblast growth factor 3 gene MP:0006013 absent endolymphatic sac IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0006013 absent endolymphatic sac IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:12810586 732330 Fgf3 fibroblast growth factor 3 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0006285 absent inner ear IAGP N RGD:5509061 20141003 MGI PMID:12810586 732330 Fgf3 fibroblast growth factor 3 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0008065 short endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0008309 dilated scala media IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8223243 732330 Fgf3 fibroblast growth factor 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14623822 732330 Fgf3 fibroblast growth factor 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732330 Fgf3 fibroblast growth factor 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17855431 732330 Fgf3 fibroblast growth factor 3 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20170511 MGI PMID:26666435 732330 Fgf3 fibroblast growth factor 3 gene MP:0012182 abnormal presomitic mesoderm morphology IAGP N RGD:5509061 20170511 MGI PMID:26666435 732333 Ccnf cyclin F gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0001889 delayed brain development IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0012090 midbrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14993286 732333 Ccnf cyclin F gene MP:0013169 small hindlimb buds IAGP N RGD:5509061 20150521 MGI PMID:14993286 732336 Serpina10 serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 10 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18344422 732336 Serpina10 serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 10 gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:18344422 732336 Serpina10 serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 10 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18344422 732336 Serpina10 serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 10 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18344422 732336 Serpina10 serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 10 gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:18344422 732338 Kcnk13 potassium channel, subfamily K, member 13 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20180607 MGI PMID:29290552 732338 Kcnk13 potassium channel, subfamily K, member 13 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 732338 Kcnk13 potassium channel, subfamily K, member 13 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20181227 MGI 732338 Kcnk13 potassium channel, subfamily K, member 13 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 732338 Kcnk13 potassium channel, subfamily K, member 13 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20180607 MGI PMID:29290552 732338 Kcnk13 potassium channel, subfamily K, member 13 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 732342 Aoc1 amine oxidase, copper-containing 1 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20201022 MGI 732342 Aoc1 amine oxidase, copper-containing 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 732342 Aoc1 amine oxidase, copper-containing 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 732342 Aoc1 amine oxidase, copper-containing 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20160421 MGI 732342 Aoc1 amine oxidase, copper-containing 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 732342 Aoc1 amine oxidase, copper-containing 1 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20210520 MGI 732343 Lox lysyl oxidase gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:12417550 732343 Lox lysyl oxidase gene MP:0000276 heart right ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 732343 Lox lysyl oxidase gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20210128 MGI 732343 Lox lysyl oxidase gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 732343 Lox lysyl oxidase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 732343 Lox lysyl oxidase gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12417550 732343 Lox lysyl oxidase gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:12417550 732343 Lox lysyl oxidase gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12417550 732343 Lox lysyl oxidase gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20141003 MGI 732343 Lox lysyl oxidase gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 732343 Lox lysyl oxidase gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 732343 Lox lysyl oxidase gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12417550 732343 Lox lysyl oxidase gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 732343 Lox lysyl oxidase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 732343 Lox lysyl oxidase gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0002625 heart left ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 732343 Lox lysyl oxidase gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20220811 MGI 732343 Lox lysyl oxidase gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 732343 Lox lysyl oxidase gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:12473682 732343 Lox lysyl oxidase gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0003907 decreased aorta elastin content IAGP N RGD:5509061 20141003 MGI PMID:12473682 732343 Lox lysyl oxidase gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:12473682 732343 Lox lysyl oxidase gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20200409 MGI PMID:29579155 732343 Lox lysyl oxidase gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20200409 MGI PMID:29579155 732343 Lox lysyl oxidase gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:12473682 732343 Lox lysyl oxidase gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:12473682 732343 Lox lysyl oxidase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0006049 semilunar valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:12417550 732343 Lox lysyl oxidase gene MP:0006083 abnormal blood vessel elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12473682 732343 Lox lysyl oxidase gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:12417550 732343 Lox lysyl oxidase gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:12473682 732343 Lox lysyl oxidase gene MP:0008418 abnormal cutaneous elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200409 MGI PMID:29579155 732343 Lox lysyl oxidase gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12417550 732343 Lox lysyl oxidase gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12473682 732343 Lox lysyl oxidase gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12417550 732343 Lox lysyl oxidase gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12473682 732343 Lox lysyl oxidase gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:12473682 732343 Lox lysyl oxidase gene MP:0009868 abnormal descending thoracic aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12473682 732343 Lox lysyl oxidase gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20200409 MGI PMID:29579155 732343 Lox lysyl oxidase gene MP:0010457 pulmonary artery stenosis IEA N RGD:5509061 20141003 MGI 732343 Lox lysyl oxidase gene MP:0010463 aorta stenosis IAGP N RGD:5509061 20141003 MGI PMID:12417550 732343 Lox lysyl oxidase gene MP:0010471 supravalvar aortic stenosis IEA N RGD:5509061 20141003 MGI 732343 Lox lysyl oxidase gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0010897 abnormal bronchiole epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0010911 abnormal pulmonary acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0010997 decreased aorta wall thickness IAGP N RGD:5509061 20141003 MGI PMID:12473682 732343 Lox lysyl oxidase gene MP:0011032 impaired branching involved in terminal bronchiole morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0011034 impaired branching involved in respiratory bronchiole morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:16192629 732343 Lox lysyl oxidase gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12417550 732343 Lox lysyl oxidase gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12473682 732343 Lox lysyl oxidase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732343 Lox lysyl oxidase gene MP:0012061 abnormal diaphragm central tendon morphology IAGP N RGD:5509061 20181108 MGI PMID:12473682 732343 Lox lysyl oxidase gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20141003 MGI PMID:12473682 732348 Ctbs chitobiase gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:22465033 732348 Ctbs chitobiase gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20231207 MGI 732348 Ctbs chitobiase gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22465033 732348 Ctbs chitobiase gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22465033 732348 Ctbs chitobiase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22465033 732351 Bin1 bridging integrator 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12773571 732351 Bin1 bridging integrator 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17210688 732351 Bin1 bridging integrator 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:12773571 732351 Bin1 bridging integrator 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17210688 732351 Bin1 bridging integrator 1 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:12773571 732351 Bin1 bridging integrator 1 gene MP:0002952 ventricular cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:12773571 732351 Bin1 bridging integrator 1 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:12773571 732351 Bin1 bridging integrator 1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:12773571 732351 Bin1 bridging integrator 1 gene MP:0004093 diffuse Z line IAGP N RGD:5509061 20141003 MGI PMID:12773571 732351 Bin1 bridging integrator 1 gene MP:0004135 abnormal mammary gland embryonic development IAGP N RGD:5509061 20141003 MGI PMID:17210688 732351 Bin1 bridging integrator 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17210688 732351 Bin1 bridging integrator 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17210688 732351 Bin1 bridging integrator 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17210688 732351 Bin1 bridging integrator 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17210688 732351 Bin1 bridging integrator 1 gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:17210688 732351 Bin1 bridging integrator 1 gene MP:0009360 endometrium inflammation IAGP N RGD:5509061 20141204 MGI PMID:17210688 732351 Bin1 bridging integrator 1 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17210688 732351 Bin1 bridging integrator 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12773571 732351 Bin1 bridging integrator 1 gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17210688 732351 Bin1 bridging integrator 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17210688 732351 Bin1 bridging integrator 1 gene MP:0030566 abnormal A band morphology IAGP N RGD:5509061 20180531 MGI PMID:12773571 732353 Slc24a1 solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20160519 MGI PMID:26246500 732353 Slc24a1 solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20160519 MGI PMID:26246500 732353 Slc24a1 solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 gene MP:0008144 nyctalopia IAGP N RGD:5509061 20160519 MGI PMID:26246500 732353 Slc24a1 solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20160519 MGI PMID:26246500 732353 Slc24a1 solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20160519 MGI PMID:26246500 732353 Slc24a1 solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 gene MP:0012034 abnormal a-wave shape IAGP N RGD:5509061 20160519 MGI PMID:26246500 732353 Slc24a1 solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 gene MP:0014333 short retina cone cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:26246500 732353 Slc24a1 solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:26246500 732357 Hrh3 histamine receptor H3 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12130692 732357 Hrh3 histamine receptor H3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15078574 732357 Hrh3 histamine receptor H3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15078574 732357 Hrh3 histamine receptor H3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12488429 732357 Hrh3 histamine receptor H3 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:12488429 732357 Hrh3 histamine receptor H3 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15078574 732357 Hrh3 histamine receptor H3 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12527809 732357 Hrh3 histamine receptor H3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21239440 732357 Hrh3 histamine receptor H3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12488429 732357 Hrh3 histamine receptor H3 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:12130692 732357 Hrh3 histamine receptor H3 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12130692 732357 Hrh3 histamine receptor H3 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:15078574 732357 Hrh3 histamine receptor H3 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:17548817 732357 Hrh3 histamine receptor H3 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:9712054 732357 Hrh3 histamine receptor H3 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:8757345 732357 Hrh3 histamine receptor H3 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:9712054 732357 Hrh3 histamine receptor H3 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:12488429 732357 Hrh3 histamine receptor H3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12488429 732357 Hrh3 histamine receptor H3 gene MP:0005447 abnormal synaptic norepinephrine release IAGP N RGD:5509061 20141003 MGI PMID:12527809 732357 Hrh3 histamine receptor H3 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:12488429 732357 Hrh3 histamine receptor H3 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:12488429 732357 Hrh3 histamine receptor H3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21239440 732357 Hrh3 histamine receptor H3 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12488429 732357 Hrh3 histamine receptor H3 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21239440 732357 Hrh3 histamine receptor H3 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12488429 732357 Hrh3 histamine receptor H3 gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:12488429 732357 Hrh3 histamine receptor H3 gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12130692 732357 Hrh3 histamine receptor H3 gene MP:0014441 decreased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:12488429 732357 Hrh3 histamine receptor H3 gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:17548817 732359 Foxj1 forkhead box J1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231116 MGI PMID:37158461 732359 Foxj1 forkhead box J1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20231116 MGI PMID:37158461 732359 Foxj1 forkhead box J1 gene MP:0000276 heart right ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 732359 Foxj1 forkhead box J1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231116 MGI PMID:37158461 732359 Foxj1 forkhead box J1 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:16325766 732359 Foxj1 forkhead box J1 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:10873152 732359 Foxj1 forkhead box J1 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20231116 MGI PMID:37158461 732359 Foxj1 forkhead box J1 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19906869 732359 Foxj1 forkhead box J1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:10873152 732359 Foxj1 forkhead box J1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:19906869 732359 Foxj1 forkhead box J1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10873152 732359 Foxj1 forkhead box J1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:10873152 732359 Foxj1 forkhead box J1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:19906869 732359 Foxj1 forkhead box J1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21745638 732359 Foxj1 forkhead box J1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141016 MGI PMID:24550157 732359 Foxj1 forkhead box J1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20190829 MGI PMID:30665704 732359 Foxj1 forkhead box J1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:21745638 732359 Foxj1 forkhead box J1 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20190829 MGI PMID:30665704 732359 Foxj1 forkhead box J1 gene MP:0002240 abnormal paranasal sinus morphology IAGP N RGD:5509061 20190829 MGI PMID:30665704 732359 Foxj1 forkhead box J1 gene MP:0002625 heart left ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 732359 Foxj1 forkhead box J1 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:19906869 732359 Foxj1 forkhead box J1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:19906869 732359 Foxj1 forkhead box J1 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:10873152 732359 Foxj1 forkhead box J1 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141016 MGI PMID:24550157 732359 Foxj1 forkhead box J1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:19906869 732359 Foxj1 forkhead box J1 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:22357932 732359 Foxj1 forkhead box J1 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:10873152 732359 Foxj1 forkhead box J1 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:16325766 732359 Foxj1 forkhead box J1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:19906869 732359 Foxj1 forkhead box J1 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:21745638 732359 Foxj1 forkhead box J1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20231116 MGI PMID:37158461 732359 Foxj1 forkhead box J1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231116 MGI PMID:37158461 732359 Foxj1 forkhead box J1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20231116 MGI PMID:37158461 732359 Foxj1 forkhead box J1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21745638 732359 Foxj1 forkhead box J1 gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:19906869 732359 Foxj1 forkhead box J1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231116 MGI PMID:37158461 732359 Foxj1 forkhead box J1 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20231116 MGI PMID:37158461 732359 Foxj1 forkhead box J1 gene MP:0010425 abnormal heart and great vessel attachment IAGP N RGD:5509061 20231116 MGI PMID:37158461 732359 Foxj1 forkhead box J1 gene MP:0010433 double inlet heart left ventricle IAGP N RGD:5509061 20231116 MGI PMID:37158461 732359 Foxj1 forkhead box J1 gene MP:0010541 aorta hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16325766 732359 Foxj1 forkhead box J1 gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20190829 MGI PMID:30665704 732359 Foxj1 forkhead box J1 gene MP:0010807 abnormal stomach position or orientation IAGP N RGD:5509061 20141003 MGI PMID:16325766 732359 Foxj1 forkhead box J1 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:16325766 732359 Foxj1 forkhead box J1 gene MP:0010854 lung situs inversus IAGP N RGD:5509061 20141003 MGI PMID:16325766 732359 Foxj1 forkhead box J1 gene MP:0011054 absent respiratory motile cilia IAGP N RGD:5509061 20141003 MGI PMID:10873152 732359 Foxj1 forkhead box J1 gene MP:0011054 absent respiratory motile cilia IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0011057 absent brain ependyma motile cilia IAGP N RGD:5509061 20141003 MGI PMID:10873152 732359 Foxj1 forkhead box J1 gene MP:0011057 absent brain ependyma motile cilia IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10873152 732359 Foxj1 forkhead box J1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21745638 732359 Foxj1 forkhead box J1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16325766 732359 Foxj1 forkhead box J1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0011252 situs inversus totalis IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0011645 absent oviduct epithelium motile cilium IAGP N RGD:5509061 20141003 MGI PMID:10873152 732359 Foxj1 forkhead box J1 gene MP:0011645 absent oviduct epithelium motile cilium IAGP N RGD:5509061 20141003 MGI PMID:9739041 732359 Foxj1 forkhead box J1 gene MP:0011998 decreased embryonic cilium length IAGP N RGD:5509061 20141003 MGI PMID:22357932 732359 Foxj1 forkhead box J1 gene MP:0012027 abnormal embryonic cilium location or orientation IAGP N RGD:5509061 20141003 MGI PMID:22357932 732359 Foxj1 forkhead box J1 gene MP:0012093 absent nodal flow IAGP N RGD:5509061 20141003 MGI PMID:22357932 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:14608379 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12588882 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20221215 MGI 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0001314 cornea opacity IEA N RGD:5509061 20240523 MGI 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:11027316 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20200514 MGI 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11027316 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12588882 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:14608379 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0002844 aortic hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:14608379 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:22354966 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22354966 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11027316 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20240523 MGI 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:22354966 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:11027316 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:11027316 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20220811 MGI 732361 Rgs2 regulator of G-protein signaling 2 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20240523 MGI 732364 Lrrc3 leucine rich repeat containing 3 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 732364 Lrrc3 leucine rich repeat containing 3 gene MP:0001257 increased body length IEA N RGD:5509061 20211021 MGI 732364 Lrrc3 leucine rich repeat containing 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 732364 Lrrc3 leucine rich repeat containing 3 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 732364 Lrrc3 leucine rich repeat containing 3 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 732364 Lrrc3 leucine rich repeat containing 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 732366 Pola1 polymerase (DNA directed), alpha 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 732367 Crisp1 cysteine-rich secretory protein 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:18571638 732369 Ntf3 neurotrophin 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:7991545 732369 Ntf3 neurotrophin 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:10188952 732369 Ntf3 neurotrophin 3 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:12441052 732369 Ntf3 neurotrophin 3 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:10195193 732369 Ntf3 neurotrophin 3 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10195193 732369 Ntf3 neurotrophin 3 gene MP:0000907 small mesencephalic trigeminal nucleus IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0000907 small mesencephalic trigeminal nucleus IAGP N RGD:5509061 20141003 MGI PMID:8208292 732369 Ntf3 neurotrophin 3 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:18305247 732369 Ntf3 neurotrophin 3 gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:7991545 732369 Ntf3 neurotrophin 3 gene MP:0000960 abnormal sensory ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:7712171 732369 Ntf3 neurotrophin 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10188952 732369 Ntf3 neurotrophin 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11684666 732369 Ntf3 neurotrophin 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12741988 732369 Ntf3 neurotrophin 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:19755105 732369 Ntf3 neurotrophin 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:22318233 732369 Ntf3 neurotrophin 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9331344 732369 Ntf3 neurotrophin 3 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:10681461 732369 Ntf3 neurotrophin 3 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:7712171 732369 Ntf3 neurotrophin 3 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:8208292 732369 Ntf3 neurotrophin 3 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11684666 732369 Ntf3 neurotrophin 3 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:10188952 732369 Ntf3 neurotrophin 3 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:10681461 732369 Ntf3 neurotrophin 3 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:23522042 732369 Ntf3 neurotrophin 3 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:9364058 732369 Ntf3 neurotrophin 3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:11684666 732369 Ntf3 neurotrophin 3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15126035 732369 Ntf3 neurotrophin 3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:22318233 732369 Ntf3 neurotrophin 3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:8208292 732369 Ntf3 neurotrophin 3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:8789944 732369 Ntf3 neurotrophin 3 gene MP:0000973 abnormal cutaneous/subcutaneous mechanoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:8789944 732369 Ntf3 neurotrophin 3 gene MP:0000985 abnormal Merkel's receptor morphology IAGP N RGD:5509061 20141003 MGI PMID:8789944 732369 Ntf3 neurotrophin 3 gene MP:0001000 absent golgi tendon organ IAGP N RGD:5509061 20141003 MGI PMID:11891988 732369 Ntf3 neurotrophin 3 gene MP:0001000 absent golgi tendon organ IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:8208292 732369 Ntf3 neurotrophin 3 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:9405689 732369 Ntf3 neurotrophin 3 gene MP:0001017 abnormal stellate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11015591 732369 Ntf3 neurotrophin 3 gene MP:0001021 small L4 dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:10188952 732369 Ntf3 neurotrophin 3 gene MP:0001021 small L4 dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:9364058 732369 Ntf3 neurotrophin 3 gene MP:0001024 small L5 dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:9405689 732369 Ntf3 neurotrophin 3 gene MP:0001024 small L5 dorsal root ganglion IAGP N RGD:5509061 20170914 MGI PMID:8208292 732369 Ntf3 neurotrophin 3 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:15126035 732369 Ntf3 neurotrophin 3 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:8208292 732369 Ntf3 neurotrophin 3 gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:8208292 732369 Ntf3 neurotrophin 3 gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:9364058 732369 Ntf3 neurotrophin 3 gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:9405689 732369 Ntf3 neurotrophin 3 gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:9364058 732369 Ntf3 neurotrophin 3 gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:9405689 732369 Ntf3 neurotrophin 3 gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:9364058 732369 Ntf3 neurotrophin 3 gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:9405689 732369 Ntf3 neurotrophin 3 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:10681461 732369 Ntf3 neurotrophin 3 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:7712171 732369 Ntf3 neurotrophin 3 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:8208292 732369 Ntf3 neurotrophin 3 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:9364058 732369 Ntf3 neurotrophin 3 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:9405689 732369 Ntf3 neurotrophin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10188952 732369 Ntf3 neurotrophin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11015591 732369 Ntf3 neurotrophin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7991545 732369 Ntf3 neurotrophin 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7712171 732369 Ntf3 neurotrophin 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10188952 732369 Ntf3 neurotrophin 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19369542 732369 Ntf3 neurotrophin 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:7712171 732369 Ntf3 neurotrophin 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:8789944 732369 Ntf3 neurotrophin 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:8208292 732369 Ntf3 neurotrophin 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10188952 732369 Ntf3 neurotrophin 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19369542 732369 Ntf3 neurotrophin 3 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:24068045 732369 Ntf3 neurotrophin 3 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:7712171 732369 Ntf3 neurotrophin 3 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:11684666 732369 Ntf3 neurotrophin 3 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:19369542 732369 Ntf3 neurotrophin 3 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:7991545 732369 Ntf3 neurotrophin 3 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:24068045 732369 Ntf3 neurotrophin 3 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:24068045 732369 Ntf3 neurotrophin 3 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:11684666 732369 Ntf3 neurotrophin 3 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:24068045 732369 Ntf3 neurotrophin 3 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0001527 athetotic walking movements IAGP N RGD:5509061 20141003 MGI PMID:8208292 732369 Ntf3 neurotrophin 3 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11015591 732369 Ntf3 neurotrophin 3 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:7991545 732369 Ntf3 neurotrophin 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24068045 732369 Ntf3 neurotrophin 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:7712171 732369 Ntf3 neurotrophin 3 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:7712171 732369 Ntf3 neurotrophin 3 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:7991545 732369 Ntf3 neurotrophin 3 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:12441052 732369 Ntf3 neurotrophin 3 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10188952 732369 Ntf3 neurotrophin 3 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10195193 732369 Ntf3 neurotrophin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10492008 732369 Ntf3 neurotrophin 3 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:11684666 732369 Ntf3 neurotrophin 3 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:7712171 732369 Ntf3 neurotrophin 3 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19369542 732369 Ntf3 neurotrophin 3 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0002726 abnormal pulmonary vein morphology IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:9364058 732369 Ntf3 neurotrophin 3 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9364058 732369 Ntf3 neurotrophin 3 gene MP:0002976 vascular smooth muscle hypotrophy IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0003228 abnormal sinus venosus morphology IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0003279 aneurysm IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:24068045 732369 Ntf3 neurotrophin 3 gene MP:0003637 cochlear ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8208292 732369 Ntf3 neurotrophin 3 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11684666 732369 Ntf3 neurotrophin 3 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9364058 732369 Ntf3 neurotrophin 3 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:11015591 732369 Ntf3 neurotrophin 3 gene MP:0003986 small cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:9405689 732369 Ntf3 neurotrophin 3 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:18305247 732369 Ntf3 neurotrophin 3 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:9331344 732369 Ntf3 neurotrophin 3 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:8208292 732369 Ntf3 neurotrophin 3 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10188952 732369 Ntf3 neurotrophin 3 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12741988 732369 Ntf3 neurotrophin 3 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22318233 732369 Ntf3 neurotrophin 3 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:7991545 732369 Ntf3 neurotrophin 3 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9331344 732369 Ntf3 neurotrophin 3 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:12441052 732369 Ntf3 neurotrophin 3 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:10188952 732369 Ntf3 neurotrophin 3 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11015591 732369 Ntf3 neurotrophin 3 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:8208292 732369 Ntf3 neurotrophin 3 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0008467 absent proprioceptive neurons IAGP N RGD:5509061 20141003 MGI PMID:11684666 732369 Ntf3 neurotrophin 3 gene MP:0008467 absent proprioceptive neurons IAGP N RGD:5509061 20141003 MGI PMID:12741988 732369 Ntf3 neurotrophin 3 gene MP:0008467 absent proprioceptive neurons IAGP N RGD:5509061 20141003 MGI PMID:9331344 732369 Ntf3 neurotrophin 3 gene MP:0008468 absent muscle spindles IAGP N RGD:5509061 20141003 MGI PMID:10188952 732369 Ntf3 neurotrophin 3 gene MP:0008468 absent muscle spindles IAGP N RGD:5509061 20141003 MGI PMID:11684666 732369 Ntf3 neurotrophin 3 gene MP:0008468 absent muscle spindles IAGP N RGD:5509061 20141003 MGI PMID:11891988 732369 Ntf3 neurotrophin 3 gene MP:0008468 absent muscle spindles IAGP N RGD:5509061 20141003 MGI PMID:12741988 732369 Ntf3 neurotrophin 3 gene MP:0008468 absent muscle spindles IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0008468 absent muscle spindles IAGP N RGD:5509061 20141003 MGI PMID:8208292 732369 Ntf3 neurotrophin 3 gene MP:0008468 absent muscle spindles IAGP N RGD:5509061 20141003 MGI PMID:9331344 732369 Ntf3 neurotrophin 3 gene MP:0008486 decreased muscle spindle number IAGP N RGD:5509061 20141003 MGI PMID:10188952 732369 Ntf3 neurotrophin 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:7712171 732369 Ntf3 neurotrophin 3 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:11684666 732369 Ntf3 neurotrophin 3 gene MP:0010224 abnormal heart ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0010405 ostium secundum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0010440 anomalous pulmonary venous connection IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0010449 heart right ventricle outflow tract stenosis IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0010501 atrium myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0010557 dilated pulmonary artery IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0010558 sinus venosus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0010563 increased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0010576 premature closure of the ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0010578 abnormal heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0010581 abnormal atrium myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0010605 thick pulmonary valve cusps IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0010617 thick mitral valve cusps IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0010909 pulmonary alveolar hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8841198 732369 Ntf3 neurotrophin 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7514502 732369 Ntf3 neurotrophin 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7991545 732369 Ntf3 neurotrophin 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8789944 732369 Ntf3 neurotrophin 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9331344 732369 Ntf3 neurotrophin 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10188952 732369 Ntf3 neurotrophin 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7712171 732369 Ntf3 neurotrophin 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10188952 732369 Ntf3 neurotrophin 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9364058 732369 Ntf3 neurotrophin 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8208292 732369 Ntf3 neurotrophin 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8789944 732369 Ntf3 neurotrophin 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7991545 732369 Ntf3 neurotrophin 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9364058 732369 Ntf3 neurotrophin 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9405689 732369 Ntf3 neurotrophin 3 gene MP:0020863 abnormal suckling reflex IAGP N RGD:5509061 20220922 MGI PMID:7712171 732371 Trib3 tribbles pseudokinase 3 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23261831 732371 Trib3 tribbles pseudokinase 3 gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:23261831 732371 Trib3 tribbles pseudokinase 3 gene MP:0014118 decreased pancreatic beta cell apoptosis IAGP N RGD:5509061 20161020 MGI PMID:25204656 732374 Epn2 epsin 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:23187125 732374 Epn2 epsin 2 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23187125 732374 Epn2 epsin 2 gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20160623 MGI PMID:23187125 732374 Epn2 epsin 2 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23187125 732374 Epn2 epsin 2 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23187125 732374 Epn2 epsin 2 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0009577 abnormal developmental vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23187125 732374 Epn2 epsin 2 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:23187125 732374 Epn2 epsin 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19666558 732374 Epn2 epsin 2 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:23187125 732374 Epn2 epsin 2 gene MP:0020161 increased vascular endothelial cell proliferation IAGP N RGD:5509061 20160623 MGI PMID:23187125 732375 Vip vasoactive intestinal polypeptide gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17309917 732375 Vip vasoactive intestinal polypeptide gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:17309917 732375 Vip vasoactive intestinal polypeptide gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:17592029 732375 Vip vasoactive intestinal polypeptide gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17309917 732375 Vip vasoactive intestinal polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17309917 732375 Vip vasoactive intestinal polypeptide gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 732375 Vip vasoactive intestinal polypeptide gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17592029 732375 Vip vasoactive intestinal polypeptide gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17592029 732375 Vip vasoactive intestinal polypeptide gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20141003 MGI PMID:17309917 732375 Vip vasoactive intestinal polypeptide gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17309917 732375 Vip vasoactive intestinal polypeptide gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:17592029 732375 Vip vasoactive intestinal polypeptide gene MP:0010758 increased right ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:17309917 732375 Vip vasoactive intestinal polypeptide gene MP:0014269 decreased testes secretion IAGP N RGD:5509061 20230810 MGI PMID:17592029 732375 Vip vasoactive intestinal polypeptide gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:12855416 732375 Vip vasoactive intestinal polypeptide gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:12855416 732375 Vip vasoactive intestinal polypeptide gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:12855416 732378 Fez1 fasciculation and elongation protein zeta 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18647754 732378 Fez1 fasciculation and elongation protein zeta 1 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:18647754 732378 Fez1 fasciculation and elongation protein zeta 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18647754 732378 Fez1 fasciculation and elongation protein zeta 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18647754 732378 Fez1 fasciculation and elongation protein zeta 1 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:18647754 732378 Fez1 fasciculation and elongation protein zeta 1 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:18647754 732378 Fez1 fasciculation and elongation protein zeta 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:18647754 732378 Fez1 fasciculation and elongation protein zeta 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:18647754 732382 Cpe carboxypeptidase E gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177043 732382 Cpe carboxypeptidase E gene MP:0000189 hypoglycemia IEA N RGD:5509061 20111116 MGI 732382 Cpe carboxypeptidase E gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 732382 Cpe carboxypeptidase E gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 732382 Cpe carboxypeptidase E gene MP:0000505 decreased digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:9893169 732382 Cpe carboxypeptidase E gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 732382 Cpe carboxypeptidase E gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:2250094 732382 Cpe carboxypeptidase E gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 732382 Cpe carboxypeptidase E gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 732382 Cpe carboxypeptidase E gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 732382 Cpe carboxypeptidase E gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220519 MGI 732382 Cpe carboxypeptidase E gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:8177043 732382 Cpe carboxypeptidase E gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177042 732382 Cpe carboxypeptidase E gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177043 732382 Cpe carboxypeptidase E gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:2250094 732382 Cpe carboxypeptidase E gene MP:0001752 abnormal hypothalamus secretion IAGP N RGD:5509061 20141003 MGI PMID:12270926 732382 Cpe carboxypeptidase E gene MP:0001752 abnormal hypothalamus secretion IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:2250094 732382 Cpe carboxypeptidase E gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 732382 Cpe carboxypeptidase E gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:2250094 732382 Cpe carboxypeptidase E gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:7663508 732382 Cpe carboxypeptidase E gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 732382 Cpe carboxypeptidase E gene MP:0002608 increased hematocrit IEA N RGD:5509061 20210826 MGI 732382 Cpe carboxypeptidase E gene MP:0002664 decreased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:9144234 732382 Cpe carboxypeptidase E gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15870393 732382 Cpe carboxypeptidase E gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20211021 MGI 732382 Cpe carboxypeptidase E gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20210128 MGI 732382 Cpe carboxypeptidase E gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 732382 Cpe carboxypeptidase E gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20211021 MGI 732382 Cpe carboxypeptidase E gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:12270926 732382 Cpe carboxypeptidase E gene MP:0003973 increased pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:9144234 732382 Cpe carboxypeptidase E gene MP:0004262 abnormal physical strength IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0004732 decreased circulating gastrin level IAGP N RGD:5509061 20141003 MGI PMID:9893169 732382 Cpe carboxypeptidase E gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 732382 Cpe carboxypeptidase E gene MP:0005117 increased circulating pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:9019408 732382 Cpe carboxypeptidase E gene MP:0005117 increased circulating pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:9144234 732382 Cpe carboxypeptidase E gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:9144234 732382 Cpe carboxypeptidase E gene MP:0005137 increased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:9144234 732382 Cpe carboxypeptidase E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177043 732382 Cpe carboxypeptidase E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15870393 732382 Cpe carboxypeptidase E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177042 732382 Cpe carboxypeptidase E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8177043 732382 Cpe carboxypeptidase E gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:2250094 732382 Cpe carboxypeptidase E gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7663508 732382 Cpe carboxypeptidase E gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20210520 MGI 732382 Cpe carboxypeptidase E gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:15870393 732382 Cpe carboxypeptidase E gene MP:0005457 abnormal percent body fat/body weight IAGP N RGD:5509061 20160407 MGI PMID:2250094 732382 Cpe carboxypeptidase E gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:12270926 732382 Cpe carboxypeptidase E gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:2250094 732382 Cpe carboxypeptidase E gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15870393 732382 Cpe carboxypeptidase E gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20240523 MGI 732382 Cpe carboxypeptidase E gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0009167 increased pancreatic islet number IEA N RGD:5509061 20111116 MGI 732382 Cpe carboxypeptidase E gene MP:0009255 degranulated pancreatic beta cells IAGP N RGD:5509061 20141003 MGI PMID:2250094 732382 Cpe carboxypeptidase E gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15870393 732382 Cpe carboxypeptidase E gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:2250094 732382 Cpe carboxypeptidase E gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:15358678 732382 Cpe carboxypeptidase E gene MP:0010463 aorta stenosis IEA N RGD:5509061 20210520 MGI 732382 Cpe carboxypeptidase E gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:12270926 732382 Cpe carboxypeptidase E gene MP:0011940 decreased food intake IEA N RGD:5509061 20210128 MGI 732382 Cpe carboxypeptidase E gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16263795 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20201231 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20098430 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16263795 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16263795 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11526402 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20098430 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:11526402 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11526402 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11526402 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16286020 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16263795 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20200402 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:20098430 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11526402 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16286020 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11526402 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16286020 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11526402 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11526402 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20200402 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0008127 decreased dendritic cell number IEA N RGD:5509061 20201231 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:16286020 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21642988 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:11526402 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16286020 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16286020 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0008346 increased gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0008524 increased plasmacytoid dendritic cell number IEA N RGD:5509061 20201231 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20098430 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:20098430 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IEA N RGD:5509061 20201022 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20201022 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0012767 increased KLRG1-positive NK cell number IEA N RGD:5509061 20170105 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0013025 increased Ly6C low monocyte number IEA N RGD:5509061 20181227 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0013417 decreased memory-marker gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0013433 increased KLRG1-positive CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0013522 decreased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20201231 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0013666 decreased immature NK cell number IEA N RGD:5509061 20201231 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0013669 decreased Ly6C-positive immature NK cell number IEA N RGD:5509061 20201231 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0013673 increased mature NK cell number IEA N RGD:5509061 20201231 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0013679 increased Ly6C-positive NK T cell number IEA N RGD:5509061 20201231 MGI 732383 Arhgef1 Rho guanine nucleotide exchange factor 1 gene MP:0014470 abnormal B cell migration IAGP N RGD:5509061 20240613 MGI PMID:16286020 732386 Uox urate oxidase gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:11474184 732386 Uox urate oxidase gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:11474184 732386 Uox urate oxidase gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20230601 MGI 732386 Uox urate oxidase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11474184 732386 Uox urate oxidase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0002083 premature death IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11474184 732386 Uox urate oxidase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:11474184 732386 Uox urate oxidase gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:11474184 732386 Uox urate oxidase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0003450 enlarged pancreas IEA N RGD:5509061 20230601 MGI 732386 Uox urate oxidase gene MP:0003619 abnormal urine color IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0004247 small pancreas IEA N RGD:5509061 20230601 MGI 732386 Uox urate oxidase gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11474184 732386 Uox urate oxidase gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:11474184 732386 Uox urate oxidase gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 732386 Uox urate oxidase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:11474184 732386 Uox urate oxidase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11474184 732386 Uox urate oxidase gene MP:0009644 uremia IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0009645 crystalluria IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0009810 increased urine uric acid level IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0009810 increased urine uric acid level IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 732386 Uox urate oxidase gene MP:0011291 nephron necrosis IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0011425 abnormal kidney interstitium morphology IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:8290593 732386 Uox urate oxidase gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0011625 cystolithiasis IAGP N RGD:5509061 20141003 MGI PMID:11316859 732386 Uox urate oxidase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20240523 MGI 732386 Uox urate oxidase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20240523 MGI 732386 Uox urate oxidase gene MP:0014117 increased pancreatic beta cell apoptosis IAGP N RGD:5509061 20210225 MGI PMID:28729031 732386 Uox urate oxidase gene MP:0020087 increased susceptibility to non-insulin-dependent diabetes IAGP N RGD:5509061 20210225 MGI PMID:28729031 732387 Slc17a1 solute carrier family 17 (sodium phosphate), member 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 732387 Slc17a1 solute carrier family 17 (sodium phosphate), member 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15837621 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20308544 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:20106865 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:20106865 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:20106865 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:20106865 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:15837621 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:20106865 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20106865 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:15837621 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:15837621 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837621 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837621 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20308544 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20308544 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20106865 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:15837621 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:20308544 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20181227 MGI 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20308544 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:20106865 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15837621 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:20106865 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:20308544 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20308544 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20308544 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20308544 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20106865 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15837621 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0011195 increased hair follicle apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20106865 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20308544 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:15837621 732388 Fntb farnesyltransferase, CAAX box, beta gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:20308544 732390 Dars1 aspartyl-tRNA synthetase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20170824 MGI PMID:27816769 732390 Dars1 aspartyl-tRNA synthetase 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20170824 MGI PMID:27816769 732390 Dars1 aspartyl-tRNA synthetase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170824 MGI PMID:27816769 732393 Paics phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoribosylaminoimidazole, succinocarboxamide synthetase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 732393 Paics phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoribosylaminoimidazole, succinocarboxamide synthetase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732393 Paics phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoribosylaminoimidazole, succinocarboxamide synthetase gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0001265 decreased body size IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20181227 MGI 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20191128 MGI 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191128 MGI 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191128 MGI 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0002083 premature death IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20240606 MGI PMID:31239271 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20191128 MGI 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20240606 MGI PMID:31239271 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0009331 absent primitive node IEA N RGD:5509061 20191128 MGI 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20240606 MGI PMID:31239271 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20240606 MGI PMID:31239271 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0010156 abnormal small intestinal crypt cell physiology IAGP N RGD:5509061 20240606 MGI PMID:31239271 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0010157 abnormal small intestinal crypt cell proliferation IAGP N RGD:5509061 20240606 MGI PMID:31239271 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20150122 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0012724 absent head fold IEA N RGD:5509061 20191128 MGI 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20181227 MGI 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:25063677 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20240606 MGI PMID:31239271 732394 Rab11a RAB11A, member RAS oncogene family gene MP:0014433 increased cytokine level IAGP N RGD:5509061 20240606 MGI PMID:31239271 732395 Sh2b2 SH2B adaptor protein 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14993264 732395 Sh2b2 SH2B adaptor protein 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14578283 732395 Sh2b2 SH2B adaptor protein 2 gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:14993264 732395 Sh2b2 SH2B adaptor protein 2 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:14993264 732397 Jup junction plakoglobin gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20221215 MGI 732397 Jup junction plakoglobin gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:8858175 732397 Jup junction plakoglobin gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20150910 MGI PMID:22021931 732397 Jup junction plakoglobin gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:22036570 732397 Jup junction plakoglobin gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:8858175 732397 Jup junction plakoglobin gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:22036570 732397 Jup junction plakoglobin gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20161027 MGI PMID:25705887 732397 Jup junction plakoglobin gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0001218 thin epidermis IAGP N RGD:5509061 20161027 MGI PMID:25705887 732397 Jup junction plakoglobin gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0001241 absent epidermis stratum corneum IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0001523 impaired righting response IEA N RGD:5509061 20240523 MGI 732397 Jup junction plakoglobin gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 732397 Jup junction plakoglobin gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 732397 Jup junction plakoglobin gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20150910 MGI PMID:22021931 732397 Jup junction plakoglobin gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:8858175 732397 Jup junction plakoglobin gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20161027 MGI PMID:25705887 732397 Jup junction plakoglobin gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:8858175 732397 Jup junction plakoglobin gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:8858175 732397 Jup junction plakoglobin gene MP:0003064 decreased coping response IEA N RGD:5509061 20170105 MGI 732397 Jup junction plakoglobin gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:8858175 732397 Jup junction plakoglobin gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8858175 732397 Jup junction plakoglobin gene MP:0004070 abnormal P wave IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0004093 diffuse Z line IAGP N RGD:5509061 20180531 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0004241 acantholysis IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8858175 732397 Jup junction plakoglobin gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:8858175 732397 Jup junction plakoglobin gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0005421 loose skin IAGP N RGD:5509061 20161027 MGI PMID:25705887 732397 Jup junction plakoglobin gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20161027 MGI PMID:25705887 732397 Jup junction plakoglobin gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160421 MGI 732397 Jup junction plakoglobin gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:22036570 732397 Jup junction plakoglobin gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:8858175 732397 Jup junction plakoglobin gene MP:0006268 absent cardiac desmosomes IAGP N RGD:5509061 20141003 MGI PMID:8858175 732397 Jup junction plakoglobin gene MP:0006268 absent cardiac desmosomes IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22036570 732397 Jup junction plakoglobin gene MP:0008727 increased heart right atrium size IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20150910 MGI PMID:22021931 732397 Jup junction plakoglobin gene MP:0009684 abnormal spinal cord lateral motor column morphology IAGP N RGD:5509061 20141003 MGI PMID:22036570 732397 Jup junction plakoglobin gene MP:0009685 abnormal spinal cord motor column morphology IAGP N RGD:5509061 20141003 MGI PMID:22036570 732397 Jup junction plakoglobin gene MP:0009686 abnormal spinal cord medial motor column morphology IAGP N RGD:5509061 20141003 MGI PMID:22036570 732397 Jup junction plakoglobin gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0010394 decreased QRS amplitude IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0010421 ventricular aneurysm IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0010534 calcified myocardium IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0010563 increased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:21880664 732397 Jup junction plakoglobin gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20150910 MGI PMID:22021931 732397 Jup junction plakoglobin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20161027 MGI PMID:25705887 732397 Jup junction plakoglobin gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20150910 MGI PMID:22021931 732397 Jup junction plakoglobin gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22036570 732397 Jup junction plakoglobin gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22036570 732397 Jup junction plakoglobin gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8858175 732397 Jup junction plakoglobin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732397 Jup junction plakoglobin gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22036570 732397 Jup junction plakoglobin gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20150910 MGI PMID:22021931 732397 Jup junction plakoglobin gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20150910 MGI PMID:22021931 732397 Jup junction plakoglobin gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:8858175 732397 Jup junction plakoglobin gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 732397 Jup junction plakoglobin gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20201210 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0021103 abnormal ventral interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:22036570 732397 Jup junction plakoglobin gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:22036570 732397 Jup junction plakoglobin gene MP:0031147 abnormal ventricular thrombosis IAGP N RGD:5509061 20201210 MGI PMID:8954745 732397 Jup junction plakoglobin gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:21245375 732397 Jup junction plakoglobin gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:22021931 732400 Rtn1 reticulon 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190221 MGI PMID:28733667 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23976996 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:23976996 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:15292239 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16630581 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20835229 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:17664350 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23976996 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:21402784 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:23976996 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:20835229 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17664350 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23976996 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0003405 abnormal platelet shape IAGP N RGD:5509061 20141003 MGI PMID:17664350 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:20835229 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0004258 abnormal placenta size IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20835229 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:17664350 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:23976996 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0005161 hematuria IAGP N RGD:5509061 20141003 MGI PMID:23976996 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:21402784 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:21402784 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:23976996 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:17664350 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:17664350 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:15555549 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20835229 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:21402784 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:21402784 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:23976996 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:20835229 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17664350 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16630581 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23976996 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15292239 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15555549 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23976996 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15292239 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:21402784 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:21402784 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:20679233 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011525 abnormal placenta intervillous maternal lacunae morphology IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011526 abnormal placenta fetal blood space morphology IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011868 podocyte microvillus transformation IAGP N RGD:5509061 20141003 MGI PMID:21402784 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15555549 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21908426 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:23976996 732402 Myh9 myosin, heavy polypeptide 9, non-muscle gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20230615 MGI PMID:20679233 732403 Prdx3 peroxiredoxin 3 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17316558 732403 Prdx3 peroxiredoxin 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17316558 732403 Prdx3 peroxiredoxin 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17316558 732403 Prdx3 peroxiredoxin 3 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0008902 abnormal renal fat pad morphology IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0011169 abnormal white fat cell differentation IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20160804 MGI PMID:21902452 732403 Prdx3 peroxiredoxin 3 gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:21902452 732404 Fgf21 fibroblast growth factor 21 gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19589869 732404 Fgf21 fibroblast growth factor 21 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:19541642 732404 Fgf21 fibroblast growth factor 21 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:22374976 732404 Fgf21 fibroblast growth factor 21 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19589869 732404 Fgf21 fibroblast growth factor 21 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180111 MGI PMID:22302939 732404 Fgf21 fibroblast growth factor 21 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0001553 abnormal circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19589869 732404 Fgf21 fibroblast growth factor 21 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19589869 732404 Fgf21 fibroblast growth factor 21 gene MP:0001752 abnormal hypothalamus secretion IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19589869 732404 Fgf21 fibroblast growth factor 21 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19541642 732404 Fgf21 fibroblast growth factor 21 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:19589869 732404 Fgf21 fibroblast growth factor 21 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19589869 732404 Fgf21 fibroblast growth factor 21 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19589869 732404 Fgf21 fibroblast growth factor 21 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:19541642 732404 Fgf21 fibroblast growth factor 21 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:22374976 732404 Fgf21 fibroblast growth factor 21 gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:19541642 732404 Fgf21 fibroblast growth factor 21 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0004357 long tibia IAGP N RGD:5509061 20141003 MGI PMID:22374976 732404 Fgf21 fibroblast growth factor 21 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:22374976 732404 Fgf21 fibroblast growth factor 21 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:22374976 732404 Fgf21 fibroblast growth factor 21 gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:22374976 732404 Fgf21 fibroblast growth factor 21 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19541642 732404 Fgf21 fibroblast growth factor 21 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20180111 MGI PMID:22302939 732404 Fgf21 fibroblast growth factor 21 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19541642 732404 Fgf21 fibroblast growth factor 21 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20170608 MGI PMID:27853148 732404 Fgf21 fibroblast growth factor 21 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:22374976 732404 Fgf21 fibroblast growth factor 21 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:19589869 732404 Fgf21 fibroblast growth factor 21 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:19589869 732404 Fgf21 fibroblast growth factor 21 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19541642 732404 Fgf21 fibroblast growth factor 21 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20170608 MGI PMID:27853148 732404 Fgf21 fibroblast growth factor 21 gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19589869 732404 Fgf21 fibroblast growth factor 21 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0009132 abnormal white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19589869 732404 Fgf21 fibroblast growth factor 21 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19589869 732404 Fgf21 fibroblast growth factor 21 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:19819944 732404 Fgf21 fibroblast growth factor 21 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:22302939 732404 Fgf21 fibroblast growth factor 21 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20170608 MGI PMID:27853148 732404 Fgf21 fibroblast growth factor 21 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20170608 MGI PMID:27853148 732404 Fgf21 fibroblast growth factor 21 gene MP:0020309 increased creatine kinase activity IAGP N RGD:5509061 20180111 MGI PMID:22302939 732405 Pln phospholamban gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20170601 MGI PMID:27114035 732405 Pln phospholamban gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20170831 MGI PMID:26644582 732405 Pln phospholamban gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10555147 732405 Pln phospholamban gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16814319 732405 Pln phospholamban gene MP:0001627 abnormal cardiac output IAGP N RGD:5509061 20141003 MGI PMID:16814319 732405 Pln phospholamban gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16814319 732405 Pln phospholamban gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20171012 MGI PMID:27936050 732405 Pln phospholamban gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20171012 MGI PMID:27936050 732405 Pln phospholamban gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:11306600 732405 Pln phospholamban gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:16814319 732405 Pln phospholamban gene MP:0002833 increased heart weight IAGP N RGD:5509061 20170601 MGI PMID:27114035 732405 Pln phospholamban gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:16814319 732405 Pln phospholamban gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10988285 732405 Pln phospholamban gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16814319 732405 Pln phospholamban gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:16461894 732405 Pln phospholamban gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:16814319 732405 Pln phospholamban gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:10988285 732405 Pln phospholamban gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:16461894 732405 Pln phospholamban gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20170601 MGI PMID:27114035 732405 Pln phospholamban gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16814319 732405 Pln phospholamban gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:16814319 732405 Pln phospholamban gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20171012 MGI PMID:27936050 732405 Pln phospholamban gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:10555147 732405 Pln phospholamban gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16814319 732405 Pln phospholamban gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10555147 732405 Pln phospholamban gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10644605 732405 Pln phospholamban gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16461894 732405 Pln phospholamban gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:8062415 732405 Pln phospholamban gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:16814319 732405 Pln phospholamban gene MP:0008543 atrial fibrillation IAGP N RGD:5509061 20141003 MGI PMID:22828895 732405 Pln phospholamban gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20170601 MGI PMID:27114035 732405 Pln phospholamban gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:8062415 732405 Pln phospholamban gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170831 MGI PMID:26644582 732405 Pln phospholamban gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:16814319 732405 Pln phospholamban gene MP:0020346 abnormal myocardial fiber calcium currents IAGP N RGD:5509061 20170601 MGI PMID:27114035 732405 Pln phospholamban gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:16814319 732405 Pln phospholamban gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:16814319 732411 Rpl10a ribosomal protein L10A gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20221201 MGI PMID:36123354 732411 Rpl10a ribosomal protein L10A gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20221201 MGI PMID:36123354 732411 Rpl10a ribosomal protein L10A gene MP:0000565 oligodactyly IAGP N RGD:5509061 20221201 MGI PMID:36123354 732411 Rpl10a ribosomal protein L10A gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20221201 MGI PMID:36123354 732411 Rpl10a ribosomal protein L10A gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20221201 MGI PMID:36123354 732411 Rpl10a ribosomal protein L10A gene MP:0001785 edema IAGP N RGD:5509061 20221201 MGI PMID:36123354 732411 Rpl10a ribosomal protein L10A gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20221201 MGI PMID:36123354 732411 Rpl10a ribosomal protein L10A gene MP:0003054 spina bifida IAGP N RGD:5509061 20221201 MGI PMID:36123354 732411 Rpl10a ribosomal protein L10A gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20221201 MGI PMID:36123354 732411 Rpl10a ribosomal protein L10A gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20221201 MGI PMID:36123354 732411 Rpl10a ribosomal protein L10A gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20221201 MGI PMID:36123354 732411 Rpl10a ribosomal protein L10A gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20221201 MGI PMID:36123354 732411 Rpl10a ribosomal protein L10A gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20221201 MGI PMID:36123354 732411 Rpl10a ribosomal protein L10A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221201 MGI PMID:36123354 732411 Rpl10a ribosomal protein L10A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20221201 MGI PMID:36123354 732411 Rpl10a ribosomal protein L10A gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20221201 MGI PMID:36123354 732413 Rbbp7 retinoblastoma binding protein 7, chromatin remodeling factor gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20160804 MGI 732413 Rbbp7 retinoblastoma binding protein 7, chromatin remodeling factor gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20111116 MGI 732413 Rbbp7 retinoblastoma binding protein 7, chromatin remodeling factor gene MP:0002084 abnormal developmental patterning IEA N RGD:5509061 20111116 MGI 732413 Rbbp7 retinoblastoma binding protein 7, chromatin remodeling factor gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20160804 MGI 732415 Cxcl1 C-X-C motif chemokine ligand 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 732415 Cxcl1 C-X-C motif chemokine ligand 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20231207 MGI 732415 Cxcl1 C-X-C motif chemokine ligand 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 732415 Cxcl1 C-X-C motif chemokine ligand 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 732415 Cxcl1 C-X-C motif chemokine ligand 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 732415 Cxcl1 C-X-C motif chemokine ligand 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:16565511 732415 Cxcl1 C-X-C motif chemokine ligand 1 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16565511 732415 Cxcl1 C-X-C motif chemokine ligand 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 732417 Rpe65 retinal pigment epithelium 65 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20160804 MGI 732417 Rpe65 retinal pigment epithelium 65 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20160804 MGI 732417 Rpe65 retinal pigment epithelium 65 gene MP:0001317 abnormal pupil morphology IEA N RGD:5509061 20141003 MGI 732417 Rpe65 retinal pigment epithelium 65 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20141003 MGI 732417 Rpe65 retinal pigment epithelium 65 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:21224384 732417 Rpe65 retinal pigment epithelium 65 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:9843205 732417 Rpe65 retinal pigment epithelium 65 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:21224384 732417 Rpe65 retinal pigment epithelium 65 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160804 MGI 732417 Rpe65 retinal pigment epithelium 65 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20160804 MGI 732417 Rpe65 retinal pigment epithelium 65 gene MP:0001513 limb grasping IEA N RGD:5509061 20141003 MGI 732417 Rpe65 retinal pigment epithelium 65 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:20007830 732417 Rpe65 retinal pigment epithelium 65 gene MP:0003011 delayed dark adaptation IAGP N RGD:5509061 20141003 MGI PMID:17933883 732417 Rpe65 retinal pigment epithelium 65 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:17933883 732417 Rpe65 retinal pigment epithelium 65 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11528395 732417 Rpe65 retinal pigment epithelium 65 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:14517541 732417 Rpe65 retinal pigment epithelium 65 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17933883 732417 Rpe65 retinal pigment epithelium 65 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21052544 732417 Rpe65 retinal pigment epithelium 65 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:9843205 732417 Rpe65 retinal pigment epithelium 65 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21052544 732417 Rpe65 retinal pigment epithelium 65 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21052544 732417 Rpe65 retinal pigment epithelium 65 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17933883 732417 Rpe65 retinal pigment epithelium 65 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:10802658 732417 Rpe65 retinal pigment epithelium 65 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:14550405 732417 Rpe65 retinal pigment epithelium 65 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:20007830 732417 Rpe65 retinal pigment epithelium 65 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:24211856 732417 Rpe65 retinal pigment epithelium 65 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:9843205 732417 Rpe65 retinal pigment epithelium 65 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11528395 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18296659 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:18296659 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:20207741 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21052544 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21224384 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:24211856 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12506090 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:18296659 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21224384 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008455 abnormal retina rod cell inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:24211856 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21224384 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:9843205 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:19494204 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21224384 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:9843205 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:17933883 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:19494204 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:20207741 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:21052544 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:17933883 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:17933883 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:17933883 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:18296659 732417 Rpe65 retinal pigment epithelium 65 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:21052544 732417 Rpe65 retinal pigment epithelium 65 gene MP:0011233 abnormal vitamin A metabolism IAGP N RGD:5509061 20141003 MGI PMID:17933883 732417 Rpe65 retinal pigment epithelium 65 gene MP:0011233 abnormal vitamin A metabolism IAGP N RGD:5509061 20141003 MGI PMID:18606814 732417 Rpe65 retinal pigment epithelium 65 gene MP:0012143 decreased a-wave amplitude IEA N RGD:5509061 20240404 MGI 732417 Rpe65 retinal pigment epithelium 65 gene MP:0012149 decreased b-wave implicit time IEA N RGD:5509061 20240404 MGI 732417 Rpe65 retinal pigment epithelium 65 gene MP:0012671 retina spots IAGP N RGD:5509061 20141003 MGI PMID:21052544 732417 Rpe65 retinal pigment epithelium 65 gene MP:0031606 increased susceptibility to age-related retinal degeneration IEA N RGD:5509061 20240404 MGI 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9690472 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20220616 MGI PMID:22095884 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000140 absent vertebral pedicles IAGP N RGD:5509061 20141003 MGI PMID:17360776 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:19479951 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20220616 MGI PMID:22095884 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:9690472 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20220616 MGI PMID:22095884 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:18234727 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9690472 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9690473 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000154 rib fusion IAGP N RGD:5509061 20220616 MGI PMID:22095884 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:18234727 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:18234727 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:19897741 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:9690472 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15659488 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15659488 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:15659488 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:15659488 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:15659488 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15659488 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19897741 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:18234727 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19479951 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:9690473 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:18234727 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:19897741 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:20335362 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001921 reduced fertility IEA N RGD:5509061 20111116 MGI 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18234727 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15659488 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16436621 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9690472 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:15659488 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19479951 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12001066 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9690473 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:19897741 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19524514 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:19897741 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18234727 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18234727 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18234727 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:14960495 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19217325 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19897741 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10837254 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10837254 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10837254 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:9690473 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20220616 MGI PMID:22095884 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:9690472 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0004646 decreased cervical vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:14960495 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0004651 increased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0004653 absent caudal vertebrae IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:15659488 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:17360776 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:18234727 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:20335362 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:9690472 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:9690473 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0005227 abnormal vertebral body development IAGP N RGD:5509061 20141003 MGI PMID:9690473 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:19479951 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:19897741 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:14960495 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0008149 abnormal costovertebral joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9690472 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:18234727 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:9690473 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19479951 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18234727 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19479951 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9690472 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19897741 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19217325 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19956724 732418 Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0021138 abnormal multifidus muscle morphology IAGP N RGD:5509061 20220630 MGI PMID:22095884 732420 St18 suppression of tumorigenicity 18 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 732420 St18 suppression of tumorigenicity 18 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 732420 St18 suppression of tumorigenicity 18 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20210121 MGI PMID:32668247 732420 St18 suppression of tumorigenicity 18 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 732420 St18 suppression of tumorigenicity 18 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20210121 MGI PMID:32668247 732420 St18 suppression of tumorigenicity 18 gene MP:0003345 decreased rib number IEA N RGD:5509061 20160804 MGI 732420 St18 suppression of tumorigenicity 18 gene MP:0005036 diarrhea IAGP N RGD:5509061 20210121 MGI PMID:32668247 732420 St18 suppression of tumorigenicity 18 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20141003 MGI 732420 St18 suppression of tumorigenicity 18 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 732420 St18 suppression of tumorigenicity 18 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20210121 MGI PMID:32668247 732420 St18 suppression of tumorigenicity 18 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20210121 MGI PMID:32668247 732420 St18 suppression of tumorigenicity 18 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210121 MGI PMID:32668247 732420 St18 suppression of tumorigenicity 18 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 732420 St18 suppression of tumorigenicity 18 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20210121 MGI PMID:32668247 732420 St18 suppression of tumorigenicity 18 gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20160804 MGI 732420 St18 suppression of tumorigenicity 18 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20210121 MGI PMID:32668247 732424 Mogs mannosyl-oligosaccharide glucosidase gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20201022 MGI 732424 Mogs mannosyl-oligosaccharide glucosidase gene MP:0000467 abnormal esophagus morphology IEA N RGD:5509061 20170105 MGI 732424 Mogs mannosyl-oligosaccharide glucosidase gene MP:0000681 abnormal thyroid gland morphology IEA N RGD:5509061 20170105 MGI 732424 Mogs mannosyl-oligosaccharide glucosidase gene MP:0000709 enlarged thymus IEA N RGD:5509061 20160811 MGI 732424 Mogs mannosyl-oligosaccharide glucosidase gene MP:0001293 anophthalmia IEA N RGD:5509061 20170105 MGI 732424 Mogs mannosyl-oligosaccharide glucosidase gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20170105 MGI 732424 Mogs mannosyl-oligosaccharide glucosidase gene MP:0002282 abnormal trachea morphology IEA N RGD:5509061 20170105 MGI 732424 Mogs mannosyl-oligosaccharide glucosidase gene MP:0002544 brachydactyly IEA N RGD:5509061 20200402 MGI 732424 Mogs mannosyl-oligosaccharide glucosidase gene MP:0005313 absent adrenal gland IEA N RGD:5509061 20170105 MGI 732424 Mogs mannosyl-oligosaccharide glucosidase gene MP:0008024 absent lymph nodes IEA N RGD:5509061 20170105 MGI 732424 Mogs mannosyl-oligosaccharide glucosidase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732424 Mogs mannosyl-oligosaccharide glucosidase gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20170105 MGI 732424 Mogs mannosyl-oligosaccharide glucosidase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 732426 Fbp2 fructose bisphosphatase 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 732426 Fbp2 fructose bisphosphatase 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201231 MGI 732426 Fbp2 fructose bisphosphatase 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 732426 Fbp2 fructose bisphosphatase 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 732426 Fbp2 fructose bisphosphatase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 732431 Smpd2 sphingomyelin phosphodiesterase 2, neutral gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11997500 732432 Nupr1 nuclear protein transcription regulator 1 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:11896600 732432 Nupr1 nuclear protein transcription regulator 1 gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:18495683 732432 Nupr1 nuclear protein transcription regulator 1 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:18495683 732432 Nupr1 nuclear protein transcription regulator 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:11896600 732432 Nupr1 nuclear protein transcription regulator 1 gene MP:0005131 increased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:18495683 732432 Nupr1 nuclear protein transcription regulator 1 gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:18495683 732432 Nupr1 nuclear protein transcription regulator 1 gene MP:0005133 increased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:18495683 732432 Nupr1 nuclear protein transcription regulator 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:18495683 732432 Nupr1 nuclear protein transcription regulator 1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:11896600 732433 Itgam integrin alpha M gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14634125 732433 Itgam integrin alpha M gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:14634125 732433 Itgam integrin alpha M gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8986723 732433 Itgam integrin alpha M gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9880401 732433 Itgam integrin alpha M gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15210787 732433 Itgam integrin alpha M gene MP:0001606 impaired hematopoiesis IEA N RGD:5509061 20161201 MGI 732433 Itgam integrin alpha M gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:15210787 732433 Itgam integrin alpha M gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16872848 732433 Itgam integrin alpha M gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15585877 732433 Itgam integrin alpha M gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:11078603 732433 Itgam integrin alpha M gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16872848 732433 Itgam integrin alpha M gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:9077544 732433 Itgam integrin alpha M gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:19797524 732433 Itgam integrin alpha M gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:8986723 732433 Itgam integrin alpha M gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:9077544 732433 Itgam integrin alpha M gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:10528208 732433 Itgam integrin alpha M gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:11078603 732433 Itgam integrin alpha M gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:10528208 732433 Itgam integrin alpha M gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:14634125 732433 Itgam integrin alpha M gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:8986723 732433 Itgam integrin alpha M gene MP:0003884 decreased macrophage cell number IEA N RGD:5509061 20161201 MGI 732433 Itgam integrin alpha M gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:15210787 732433 Itgam integrin alpha M gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8986723 732433 Itgam integrin alpha M gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10528208 732433 Itgam integrin alpha M gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:16872848 732433 Itgam integrin alpha M gene MP:0005074 impaired granulocyte bactericidal activity IAGP N RGD:5509061 20141003 MGI PMID:19797524 732433 Itgam integrin alpha M gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15210787 732433 Itgam integrin alpha M gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 732433 Itgam integrin alpha M gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8986723 732433 Itgam integrin alpha M gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:9880401 732433 Itgam integrin alpha M gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15210787 732433 Itgam integrin alpha M gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15210787 732433 Itgam integrin alpha M gene MP:0008125 abnormal dendritic cell number IEA N RGD:5509061 20161201 MGI 732433 Itgam integrin alpha M gene MP:0008524 increased plasmacytoid dendritic cell number IEA N RGD:5509061 20161201 MGI 732433 Itgam integrin alpha M gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16872848 732433 Itgam integrin alpha M gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:10528208 732433 Itgam integrin alpha M gene MP:0013649 decreased CD11b-high dendritic cell number IEA N RGD:5509061 20190411 MGI 732433 Itgam integrin alpha M gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:23550035 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0001261 obese IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0001433 polyphagia IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0004512 anosmia IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18032602 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0006087 increased body mass index IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:18032602 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:18032602 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:18032602 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:18032602 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15539463 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0011281 abnormal olfactory epithelium cilium morphology IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0020582 increased ceramide level IAGP N RGD:5509061 20201210 MGI PMID:32620959 732436 Bbs2 Bardet-Biedl syndrome 2 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:15539463 732439 Cops2 COP9 signalosome subunit 2 gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20141003 MGI PMID:12972599 732439 Cops2 COP9 signalosome subunit 2 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:12972599 732439 Cops2 COP9 signalosome subunit 2 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:12972599 732439 Cops2 COP9 signalosome subunit 2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12972599 732439 Cops2 COP9 signalosome subunit 2 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:12972599 732439 Cops2 COP9 signalosome subunit 2 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20141003 MGI PMID:12972599 732439 Cops2 COP9 signalosome subunit 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12972599 732439 Cops2 COP9 signalosome subunit 2 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:12972599 732442 Txn1 thioredoxin 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:8812119 732442 Txn1 thioredoxin 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:8812119 732442 Txn1 thioredoxin 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8812119 732442 Txn1 thioredoxin 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8812119 732442 Txn1 thioredoxin 1 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:8812119 732447 Ezr ezrin gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15177033 732447 Ezr ezrin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15809309 732447 Ezr ezrin gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 732447 Ezr ezrin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15809309 732447 Ezr ezrin gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15809309 732447 Ezr ezrin gene MP:0008003 achlorhydria IAGP N RGD:5509061 20141003 MGI PMID:15809309 732447 Ezr ezrin gene MP:0008109 abnormal small intestinal microvillus morphology IAGP N RGD:5509061 20141003 MGI PMID:15809309 732447 Ezr ezrin gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19124745 732447 Ezr ezrin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15177033 732447 Ezr ezrin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15809309 732447 Ezr ezrin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732448 Lbr lamin B receptor gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0000422 delayed hair appearance IEA N RGD:5509061 20111116 MGI 732448 Lbr lamin B receptor gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0000550 abnormal forelimb morphology IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170525 MGI PMID:27483354 732448 Lbr lamin B receptor gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0001143 constricted vagina orifice IEA N RGD:5509061 20111116 MGI 732448 Lbr lamin B receptor gene MP:0001147 small testis IEA N RGD:5509061 20220519 MGI 732448 Lbr lamin B receptor gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20220519 MGI 732448 Lbr lamin B receptor gene MP:0001191 abnormal skin condition IEA N RGD:5509061 20111116 MGI 732448 Lbr lamin B receptor gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:4463225 732448 Lbr lamin B receptor gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:830768 732448 Lbr lamin B receptor gene MP:0001240 abnormal epidermis stratum corneum morphology IEA N RGD:5509061 20111116 MGI 732448 Lbr lamin B receptor gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0001282 short vibrissae IEA N RGD:5509061 20111116 MGI 732448 Lbr lamin B receptor gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0001923 reduced female fertility IEA N RGD:5509061 20111116 MGI 732448 Lbr lamin B receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0001943 abnormal respiration IEA N RGD:5509061 20111116 MGI 732448 Lbr lamin B receptor gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20111116 MGI 732448 Lbr lamin B receptor gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0002082 postnatal lethality IEA N RGD:5509061 20111116 MGI 732448 Lbr lamin B receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20111116 MGI 732448 Lbr lamin B receptor gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20170525 MGI PMID:27483354 732448 Lbr lamin B receptor gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0002286 cryptorchism IEA N RGD:5509061 20111116 MGI 732448 Lbr lamin B receptor gene MP:0002415 abnormal neutrophil differentiation IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0002429 abnormal blood cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0002670 absent scrotum IEA N RGD:5509061 20211014 MGI 732448 Lbr lamin B receptor gene MP:0002764 short tibia IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:1101484 732448 Lbr lamin B receptor gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20170525 MGI PMID:27483354 732448 Lbr lamin B receptor gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20170525 MGI PMID:27483354 732448 Lbr lamin B receptor gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20170525 MGI PMID:27483354 732448 Lbr lamin B receptor gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20170525 MGI PMID:27483354 732448 Lbr lamin B receptor gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20170525 MGI PMID:27483354 732448 Lbr lamin B receptor gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0005061 abnormal eosinophil morphology IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20170525 MGI PMID:27483354 732448 Lbr lamin B receptor gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20170525 MGI PMID:27483354 732448 Lbr lamin B receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20170525 MGI PMID:27483354 732448 Lbr lamin B receptor gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20141003 MGI PMID:830768 732448 Lbr lamin B receptor gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22105998 732448 Lbr lamin B receptor gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0008890 abnormal nuclear lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0009606 increased keratohyalin granule size IAGP N RGD:5509061 20141003 MGI PMID:830768 732448 Lbr lamin B receptor gene MP:0009611 epidermis stratum spinosum hyperplasia IEA N RGD:5509061 20111116 MGI 732448 Lbr lamin B receptor gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20180524 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 732448 Lbr lamin B receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17403717 732448 Lbr lamin B receptor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12490533 732448 Lbr lamin B receptor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18621876 732448 Lbr lamin B receptor gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 732448 Lbr lamin B receptor gene MP:0013178 tail necrosis IEA N RGD:5509061 20141003 MGI 732448 Lbr lamin B receptor gene MP:0020351 decreased vocalization IEA N RGD:5509061 20161013 MGI 732448 Lbr lamin B receptor gene MP:0030571 dilated piliary canal IAGP N RGD:5509061 20180524 MGI PMID:12490533 732449 Nphs2 nephrosis 2, podocin gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0002083 premature death IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0003606 kidney failure IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0011309 abnormal kidney arterial blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0011321 abnormal peritubular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:19713307 732449 Nphs2 nephrosis 2, podocin gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0011454 abnormal glomerular endothelium fenestra morphology IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0011470 increased urine creatinine level IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0011509 dilated glomerular capillary IAGP N RGD:5509061 20141003 MGI PMID:18288100 732449 Nphs2 nephrosis 2, podocin gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20190725 MGI PMID:29049388 732449 Nphs2 nephrosis 2, podocin gene MP:0011868 podocyte microvillus transformation IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0011871 podocyte hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:14701729 732449 Nphs2 nephrosis 2, podocin gene MP:0011871 podocyte hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19713307 732452 Rps6ka1 ribosomal protein S6 kinase polypeptide 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 732452 Rps6ka1 ribosomal protein S6 kinase polypeptide 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20181227 MGI 732453 Adar adenosine deaminase, RNA-specific gene MP:0000239 absent common myeloid progenitor cells IAGP N RGD:5509061 20141003 MGI PMID:14615479 732453 Adar adenosine deaminase, RNA-specific gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19060901 732453 Adar adenosine deaminase, RNA-specific gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:11099415 732453 Adar adenosine deaminase, RNA-specific gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:14615479 732453 Adar adenosine deaminase, RNA-specific gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:14613934 732453 Adar adenosine deaminase, RNA-specific gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20220616 MGI PMID:34343497 732453 Adar adenosine deaminase, RNA-specific gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19060901 732453 Adar adenosine deaminase, RNA-specific gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:14615479 732453 Adar adenosine deaminase, RNA-specific gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20220616 MGI PMID:34343497 732453 Adar adenosine deaminase, RNA-specific gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230615 MGI PMID:34332594 732453 Adar adenosine deaminase, RNA-specific gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14613934 732453 Adar adenosine deaminase, RNA-specific gene MP:0001265 decreased body size IAGP N RGD:5509061 20220616 MGI PMID:34343497 732453 Adar adenosine deaminase, RNA-specific gene MP:0001265 decreased body size IAGP N RGD:5509061 20230615 MGI PMID:34332594 732453 Adar adenosine deaminase, RNA-specific gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:14613934 732453 Adar adenosine deaminase, RNA-specific gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:14613934 732453 Adar adenosine deaminase, RNA-specific gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14615479 732453 Adar adenosine deaminase, RNA-specific gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200917 MGI PMID:14613934 732453 Adar adenosine deaminase, RNA-specific gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14613934 732453 Adar adenosine deaminase, RNA-specific gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201231 MGI 732453 Adar adenosine deaminase, RNA-specific gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:14613934 732453 Adar adenosine deaminase, RNA-specific gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20220616 MGI PMID:34343497 732453 Adar adenosine deaminase, RNA-specific gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19060901 732453 Adar adenosine deaminase, RNA-specific gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:14613934 732453 Adar adenosine deaminase, RNA-specific gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:14613934 732453 Adar adenosine deaminase, RNA-specific gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20220616 MGI PMID:34343497 732453 Adar adenosine deaminase, RNA-specific gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 732453 Adar adenosine deaminase, RNA-specific gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20201231 MGI 732453 Adar adenosine deaminase, RNA-specific gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14613934 732453 Adar adenosine deaminase, RNA-specific gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14615479 732453 Adar adenosine deaminase, RNA-specific gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:11099415 732453 Adar adenosine deaminase, RNA-specific gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20201231 MGI 732453 Adar adenosine deaminase, RNA-specific gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19060901 732453 Adar adenosine deaminase, RNA-specific gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20220616 MGI PMID:34343497 732453 Adar adenosine deaminase, RNA-specific gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:14613934 732453 Adar adenosine deaminase, RNA-specific gene MP:0005376 homeostasis/metabolism phenotype IAGP N RGD:5509061 20220616 MGI PMID:34343497 732453 Adar adenosine deaminase, RNA-specific gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20220616 MGI PMID:34343497 732453 Adar adenosine deaminase, RNA-specific gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20220616 MGI PMID:34343497 732453 Adar adenosine deaminase, RNA-specific gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20201022 MGI 732453 Adar adenosine deaminase, RNA-specific gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21173229 732453 Adar adenosine deaminase, RNA-specific gene MP:0008550 abnormal circulating interferon-beta level IAGP N RGD:5509061 20141003 MGI PMID:19060901 732453 Adar adenosine deaminase, RNA-specific gene MP:0008573 increased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:19060901 732453 Adar adenosine deaminase, RNA-specific gene MP:0008591 increased circulating interleukin-1 level IAGP N RGD:5509061 20230615 MGI PMID:34332594 732453 Adar adenosine deaminase, RNA-specific gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20230615 MGI PMID:34332594 732453 Adar adenosine deaminase, RNA-specific gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20230615 MGI PMID:34332594 732453 Adar adenosine deaminase, RNA-specific gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20230615 MGI PMID:34332594 732453 Adar adenosine deaminase, RNA-specific gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:14613934 732453 Adar adenosine deaminase, RNA-specific gene MP:0010768 mortality/aging IAGP N RGD:5509061 20220616 MGI PMID:34343497 732453 Adar adenosine deaminase, RNA-specific gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19060901 732453 Adar adenosine deaminase, RNA-specific gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11099415 732453 Adar adenosine deaminase, RNA-specific gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14613934 732453 Adar adenosine deaminase, RNA-specific gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14615479 732453 Adar adenosine deaminase, RNA-specific gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21173229 732453 Adar adenosine deaminase, RNA-specific gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732453 Adar adenosine deaminase, RNA-specific gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20220616 MGI PMID:34343497 732453 Adar adenosine deaminase, RNA-specific gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20220616 MGI PMID:34343497 732453 Adar adenosine deaminase, RNA-specific gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210218 MGI PMID:14613934 732453 Adar adenosine deaminase, RNA-specific gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:14613934 732453 Adar adenosine deaminase, RNA-specific gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:21173229 732453 Adar adenosine deaminase, RNA-specific gene MP:0020952 increased susceptibility to Paramyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:21173229 732453 Adar adenosine deaminase, RNA-specific gene MP:0031226 increased CXCL10 level IAGP N RGD:5509061 20230615 MGI PMID:34332594 732455 Pla2g6 phospholipase A2, group VI gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:18305254 732455 Pla2g6 phospholipase A2, group VI gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:22442204 732455 Pla2g6 phospholipase A2, group VI gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:19893029 732455 Pla2g6 phospholipase A2, group VI gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20111116 MGI 732455 Pla2g6 phospholipase A2, group VI gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18305254 732455 Pla2g6 phospholipase A2, group VI gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19893029 732455 Pla2g6 phospholipase A2, group VI gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22442204 732455 Pla2g6 phospholipase A2, group VI gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18305254 732455 Pla2g6 phospholipase A2, group VI gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19893029 732455 Pla2g6 phospholipase A2, group VI gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20220120 MGI PMID:30088174 732455 Pla2g6 phospholipase A2, group VI gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18202189 732455 Pla2g6 phospholipase A2, group VI gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18305254 732455 Pla2g6 phospholipase A2, group VI gene MP:0001405 impaired coordination IAGP N RGD:5509061 20220120 MGI PMID:30088174 732455 Pla2g6 phospholipase A2, group VI gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18202189 732455 Pla2g6 phospholipase A2, group VI gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18305254 732455 Pla2g6 phospholipase A2, group VI gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:18202189 732455 Pla2g6 phospholipase A2, group VI gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:18202189 732455 Pla2g6 phospholipase A2, group VI gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:18202189 732455 Pla2g6 phospholipase A2, group VI gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:18305254 732455 Pla2g6 phospholipase A2, group VI gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15252026 732455 Pla2g6 phospholipase A2, group VI gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:18305254 732455 Pla2g6 phospholipase A2, group VI gene MP:0001925 male infertility IAGP N RGD:5509061 20190815 MGI PMID:25337551 732455 Pla2g6 phospholipase A2, group VI gene MP:0002001 blindness IAGP N RGD:5509061 20190815 MGI PMID:25337551 732455 Pla2g6 phospholipase A2, group VI gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:19893029 732455 Pla2g6 phospholipase A2, group VI gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18305254 732455 Pla2g6 phospholipase A2, group VI gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19893029 732455 Pla2g6 phospholipase A2, group VI gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22442204 732455 Pla2g6 phospholipase A2, group VI gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20111116 MGI 732455 Pla2g6 phospholipase A2, group VI gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:18202189 732455 Pla2g6 phospholipase A2, group VI gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:18305254 732455 Pla2g6 phospholipase A2, group VI gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22442204 732455 Pla2g6 phospholipase A2, group VI gene MP:0002269 muscular atrophy IEA N RGD:5509061 20111116 MGI 732455 Pla2g6 phospholipase A2, group VI gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18305254 732455 Pla2g6 phospholipase A2, group VI gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:21813701 732455 Pla2g6 phospholipase A2, group VI gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15252026 732455 Pla2g6 phospholipase A2, group VI gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20220120 MGI PMID:30088174 732455 Pla2g6 phospholipase A2, group VI gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20220120 MGI PMID:30088174 732455 Pla2g6 phospholipase A2, group VI gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20141003 MGI PMID:21813701 732455 Pla2g6 phospholipase A2, group VI gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20141003 MGI PMID:22442204 732455 Pla2g6 phospholipase A2, group VI gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:18202189 732455 Pla2g6 phospholipase A2, group VI gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:19893029 732455 Pla2g6 phospholipase A2, group VI gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220120 MGI PMID:30088174 732455 Pla2g6 phospholipase A2, group VI gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:21813701 732455 Pla2g6 phospholipase A2, group VI gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20190815 MGI PMID:25337551 732455 Pla2g6 phospholipase A2, group VI gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19893029 732455 Pla2g6 phospholipase A2, group VI gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:21813701 732455 Pla2g6 phospholipase A2, group VI gene MP:0005156 bradykinesia IAGP N RGD:5509061 20220120 MGI PMID:30088174 732455 Pla2g6 phospholipase A2, group VI gene MP:0005277 abnormal brainstem morphology IEA N RGD:5509061 20111116 MGI 732455 Pla2g6 phospholipase A2, group VI gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:21813701 732455 Pla2g6 phospholipase A2, group VI gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:21813701 732455 Pla2g6 phospholipase A2, group VI gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:21813701 732455 Pla2g6 phospholipase A2, group VI gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20220120 MGI PMID:30088174 732455 Pla2g6 phospholipase A2, group VI gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20220120 MGI PMID:30088174 732455 Pla2g6 phospholipase A2, group VI gene MP:0008026 abnormal brain white matter morphology IEA N RGD:5509061 20111116 MGI 732455 Pla2g6 phospholipase A2, group VI gene MP:0008503 abnormal spinal cord grey matter morphology IAGP N RGD:5509061 20141003 MGI PMID:21813701 732455 Pla2g6 phospholipase A2, group VI gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:21813701 732455 Pla2g6 phospholipase A2, group VI gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20220120 MGI PMID:30088174 732455 Pla2g6 phospholipase A2, group VI gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22442204 732455 Pla2g6 phospholipase A2, group VI gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:19893029 732455 Pla2g6 phospholipase A2, group VI gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20141003 MGI PMID:21813701 732455 Pla2g6 phospholipase A2, group VI gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19893029 732455 Pla2g6 phospholipase A2, group VI gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:22442204 732455 Pla2g6 phospholipase A2, group VI gene MP:0010331 abnormal apolipoprotein level IAGP N RGD:5509061 20190815 MGI PMID:25337551 732455 Pla2g6 phospholipase A2, group VI gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20220120 MGI PMID:30088174 732455 Pla2g6 phospholipase A2, group VI gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:21813701 732455 Pla2g6 phospholipase A2, group VI gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20220120 MGI PMID:30088174 732455 Pla2g6 phospholipase A2, group VI gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20220120 MGI PMID:30088174 732455 Pla2g6 phospholipase A2, group VI gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20220120 MGI PMID:30088174 732455 Pla2g6 phospholipase A2, group VI gene MP:0014065 Lewy bodies IAGP N RGD:5509061 20220120 MGI PMID:30088174 732455 Pla2g6 phospholipase A2, group VI gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20220120 MGI PMID:30088174 732455 Pla2g6 phospholipase A2, group VI gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20161013 MGI PMID:21813701 732456 Grina glutamate receptor, ionotropic, N-methyl D-aspartate-associated protein 1 (glutamate binding) gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10490099 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:10490099 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:15197228 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:11371356 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:9861011 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9861011 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10490100 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:20850013 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:10490099 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11371356 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:10490099 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11371356 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9861011 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:11371356 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:10490099 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:20850013 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11371356 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:11445538 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0001884 mammary gland alveolar hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11445538 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10490099 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11371356 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18322180 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10490100 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18322180 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:10490099 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:9861011 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20160218 MGI PMID:26163372 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10490099 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:10490099 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:10490100 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:11371356 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11371356 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10490099 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:18322180 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20160218 MGI PMID:26163372 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:20850013 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9861011 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10490100 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:11371356 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:20850013 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18322180 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:11445538 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:11371356 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18322180 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18322180 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18322180 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008172 abnormal follicular B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:18322180 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:15197228 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:15197228 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:10490099 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15197228 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15197228 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0010903 abnormal pulmonary alveolus wall morphology IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10490099 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10490100 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11371356 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11606785 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9861011 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210805 MGI 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0013585 thymus cortex atrophy IAGP N RGD:5509061 20150319 MGI PMID:10490099 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0013585 thymus cortex atrophy IAGP N RGD:5509061 20150319 MGI PMID:9826711 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0013590 enlarged thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:10490099 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0013590 enlarged thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:12705851 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0013741 absent thymus corticomedullary boundary IAGP N RGD:5509061 20150430 MGI PMID:9861011 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0013771 decreased effector memory T-helper cell number IAGP N RGD:5509061 20160218 MGI PMID:26163372 732457 Socs1 suppressor of cytokine signaling 1 gene MP:0031041 decreased susceptibility to Togaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:10490099 732464 Stk17b serine/threonine kinase 17b (apoptosis-inducing) gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15589167 732464 Stk17b serine/threonine kinase 17b (apoptosis-inducing) gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:15589167 732464 Stk17b serine/threonine kinase 17b (apoptosis-inducing) gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:15589167 732464 Stk17b serine/threonine kinase 17b (apoptosis-inducing) gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15589167 732464 Stk17b serine/threonine kinase 17b (apoptosis-inducing) gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:15589167 732464 Stk17b serine/threonine kinase 17b (apoptosis-inducing) gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15589167 732464 Stk17b serine/threonine kinase 17b (apoptosis-inducing) gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15589167 732464 Stk17b serine/threonine kinase 17b (apoptosis-inducing) gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15589167 732464 Stk17b serine/threonine kinase 17b (apoptosis-inducing) gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:15589167 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:16901941 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20231207 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20221215 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0000745 tremors IAGP N RGD:5509061 20151015 MGI PMID:25316793 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0000753 paralysis IAGP N RGD:5509061 20151015 MGI PMID:25316793 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151015 MGI PMID:25316793 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20151015 MGI PMID:25316793 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20151015 MGI PMID:25316793 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20151015 MGI PMID:25316793 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20181227 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:16901941 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20151015 MGI PMID:25316793 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0002895 abnormal otolithic membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20181227 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20151015 MGI PMID:25316793 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0003630 abnormal urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20151015 MGI PMID:25316793 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0003870 decreased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20211021 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20211021 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004156 abnormal QT variability IEA N RGD:5509061 20220519 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20141003 MGI PMID:16901941 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004366 abnormal strial marginal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004366 abnormal strial marginal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16901941 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004368 abnormal stria vascularis vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16901941 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004410 absent endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004438 abnormal vestibular hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16901941 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:16901941 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16901941 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:16901941 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20151015 MGI PMID:25316793 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20211021 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20210128 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20151015 MGI PMID:25316793 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20151015 MGI PMID:25316793 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20181227 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0011305 dilated kidney calyx IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0011418 leukocyturia IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0011426 abnormal ureter smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0011487 abnormal ureteropelvic junction morphology IAGP N RGD:5509061 20141003 MGI PMID:12620969 732466 Scarb2 scavenger receptor class B, member 2 gene MP:0011491 ureteropelvic junction obstruction IAGP N RGD:5509061 20141003 MGI PMID:12620969 732469 Rasa1 RAS p21 protein activator 1 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20230601 MGI 732469 Rasa1 RAS p21 protein activator 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20151015 MGI PMID:25283357 732469 Rasa1 RAS p21 protein activator 1 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:22949508 732469 Rasa1 RAS p21 protein activator 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20151015 MGI PMID:25283357 732469 Rasa1 RAS p21 protein activator 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20151015 MGI PMID:25283357 732469 Rasa1 RAS p21 protein activator 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20181227 MGI 732469 Rasa1 RAS p21 protein activator 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 732469 Rasa1 RAS p21 protein activator 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 732469 Rasa1 RAS p21 protein activator 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22949508 732469 Rasa1 RAS p21 protein activator 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20151015 MGI PMID:25283357 732469 Rasa1 RAS p21 protein activator 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0004309 absent otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0004573 absent limb buds IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20151015 MGI PMID:25283357 732469 Rasa1 RAS p21 protein activator 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210128 MGI 732469 Rasa1 RAS p21 protein activator 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230601 MGI 732469 Rasa1 RAS p21 protein activator 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 732469 Rasa1 RAS p21 protein activator 1 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:22949508 732469 Rasa1 RAS p21 protein activator 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:22949508 732469 Rasa1 RAS p21 protein activator 1 gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22949508 732469 Rasa1 RAS p21 protein activator 1 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:22949508 732469 Rasa1 RAS p21 protein activator 1 gene MP:0010662 abnormal intersomitic artery morphology IAGP N RGD:5509061 20151015 MGI PMID:25283357 732469 Rasa1 RAS p21 protein activator 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20151015 MGI PMID:25283357 732469 Rasa1 RAS p21 protein activator 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732469 Rasa1 RAS p21 protein activator 1 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20151015 MGI PMID:25283357 732469 Rasa1 RAS p21 protein activator 1 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0012761 increased cranial neural crest cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:7477259 732469 Rasa1 RAS p21 protein activator 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 732469 Rasa1 RAS p21 protein activator 1 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:22949508 732470 Galnt5 polypeptide N-acetylgalactosaminyltransferase 5 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 732472 Hck hemopoietic cell kinase gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:8125254 732472 Hck hemopoietic cell kinase gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16872848 732472 Hck hemopoietic cell kinase gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8125254 732472 Hck hemopoietic cell kinase gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:10547366 732472 Hck hemopoietic cell kinase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10547366 732472 Hck hemopoietic cell kinase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16872848 732472 Hck hemopoietic cell kinase gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0004202 pulmonary hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15067085 732472 Hck hemopoietic cell kinase gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:8634424 732472 Hck hemopoietic cell kinase gene MP:0010942 abnormal respiratory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0010944 respiratory epithelium hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0011045 decreased lung elastance IAGP N RGD:5509061 20141003 MGI PMID:12208875 732472 Hck hemopoietic cell kinase gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8634424 732474 Grb2 growth factor receptor bound protein 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20498059 732474 Grb2 growth factor receptor bound protein 2 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:9865697 732474 Grb2 growth factor receptor bound protein 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9865697 732474 Grb2 growth factor receptor bound protein 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15492213 732474 Grb2 growth factor receptor bound protein 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15492213 732474 Grb2 growth factor receptor bound protein 2 gene MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15492213 732474 Grb2 growth factor receptor bound protein 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20498059 732474 Grb2 growth factor receptor bound protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9865697 732474 Grb2 growth factor receptor bound protein 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0004868 increased endometrial carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15492213 732474 Grb2 growth factor receptor bound protein 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20498059 732474 Grb2 growth factor receptor bound protein 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20498059 732474 Grb2 growth factor receptor bound protein 2 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20498059 732474 Grb2 growth factor receptor bound protein 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20498059 732474 Grb2 growth factor receptor bound protein 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20498059 732474 Grb2 growth factor receptor bound protein 2 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0008194 abnormal memory B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0009923 decreased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21427701 732474 Grb2 growth factor receptor bound protein 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9865697 732474 Grb2 growth factor receptor bound protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732474 Grb2 growth factor receptor bound protein 2 gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20141003 MGI PMID:11369229 732474 Grb2 growth factor receptor bound protein 2 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:9865697 732474 Grb2 growth factor receptor bound protein 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15492213 732474 Grb2 growth factor receptor bound protein 2 gene MP:0020935 decreased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16314834 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:17070019 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20170105 MGI 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:17070019 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17070019 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:17070019 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20170105 MGI 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20727793 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20727793 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17070019 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17070019 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:17070019 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:17070019 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17070019 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17070019 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:20727793 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20727793 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0006057 decreased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:17070019 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17070019 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170105 MGI 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0012252 abnormal septum transversum morphology IAGP N RGD:5509061 20141003 MGI PMID:17070019 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0012509 neural tube degeneration IAGP N RGD:5509061 20141003 MGI PMID:17070019 732478 Ptpn12 protein tyrosine phosphatase, non-receptor type 12 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 732479 Ero1a endoplasmic reticulum oxidoreductase 1 alpha gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:19752026 732479 Ero1a endoplasmic reticulum oxidoreductase 1 alpha gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20308425 732479 Ero1a endoplasmic reticulum oxidoreductase 1 alpha gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:19752026 732479 Ero1a endoplasmic reticulum oxidoreductase 1 alpha gene MP:0011081 decreased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19752026 732481 Hspb1 heat shock protein 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 732481 Hspb1 heat shock protein 1 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:24143227 732481 Hspb1 heat shock protein 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:24143227 732481 Hspb1 heat shock protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17661394 732481 Hspb1 heat shock protein 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:24143227 732481 Hspb1 heat shock protein 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:24143227 732481 Hspb1 heat shock protein 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 732481 Hspb1 heat shock protein 1 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:24143227 732481 Hspb1 heat shock protein 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:24143227 732481 Hspb1 heat shock protein 1 gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:24143227 732481 Hspb1 heat shock protein 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210826 MGI 732481 Hspb1 heat shock protein 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:24143227 732481 Hspb1 heat shock protein 1 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:24143227 732481 Hspb1 heat shock protein 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:24143227 732484 Adgrl4 adhesion G protein-coupled receptor L4 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 732484 Adgrl4 adhesion G protein-coupled receptor L4 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 732484 Adgrl4 adhesion G protein-coupled receptor L4 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 732484 Adgrl4 adhesion G protein-coupled receptor L4 gene MP:0001304 cataract IEA N RGD:5509061 20210520 MGI 732484 Adgrl4 adhesion G protein-coupled receptor L4 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 732484 Adgrl4 adhesion G protein-coupled receptor L4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 732484 Adgrl4 adhesion G protein-coupled receptor L4 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 732484 Adgrl4 adhesion G protein-coupled receptor L4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 732484 Adgrl4 adhesion G protein-coupled receptor L4 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220811 MGI 732484 Adgrl4 adhesion G protein-coupled receptor L4 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 732484 Adgrl4 adhesion G protein-coupled receptor L4 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 732484 Adgrl4 adhesion G protein-coupled receptor L4 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 732484 Adgrl4 adhesion G protein-coupled receptor L4 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210520 MGI 732484 Adgrl4 adhesion G protein-coupled receptor L4 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20221222 MGI PMID:34347079 732486 Pnliprp1 pancreatic lipase related protein 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20190912 MGI PMID:21115337 732486 Pnliprp1 pancreatic lipase related protein 1 gene MP:0001261 obese IAGP N RGD:5509061 20190912 MGI PMID:21115337 732486 Pnliprp1 pancreatic lipase related protein 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20190912 MGI PMID:21115337 732486 Pnliprp1 pancreatic lipase related protein 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20190912 MGI PMID:21115337 732486 Pnliprp1 pancreatic lipase related protein 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20190912 MGI PMID:21115337 732486 Pnliprp1 pancreatic lipase related protein 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20190912 MGI PMID:21115337 732486 Pnliprp1 pancreatic lipase related protein 1 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20190912 MGI PMID:21115337 732486 Pnliprp1 pancreatic lipase related protein 1 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20190912 MGI PMID:21115337 732486 Pnliprp1 pancreatic lipase related protein 1 gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20190912 MGI PMID:21115337 732486 Pnliprp1 pancreatic lipase related protein 1 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20190912 MGI PMID:21115337 732486 Pnliprp1 pancreatic lipase related protein 1 gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20190912 MGI PMID:21115337 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16691213 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11883932 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:16528383 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:16691213 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15606898 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23717413 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15606898 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16528383 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12205028 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:15606898 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:16691213 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16691213 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16294209 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:18250473 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11274171 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12205028 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11883932 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12205028 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:16528383 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:11274171 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:16294209 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:15606898 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:21094133 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16691213 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12205028 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18250473 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0006110 ventricular fibrillation IAGP N RGD:5509061 20141003 MGI PMID:16528383 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:18250473 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12651621 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12651621 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18250473 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:16528383 732488 Tgm2 transglutaminase 2, C polypeptide gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:18250473 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19409815 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20152175 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:20152175 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12077299 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12077299 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12077299 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17023430 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:14528298 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18084302 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:18084302 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:19409815 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19409815 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19409815 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:14528298 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:14528298 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:19409815 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19409815 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19409815 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19409815 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0008176 abnormal germinal center B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21642988 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21642988 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17023430 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19409815 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21642988 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:14528298 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12077299 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12077299 732492 Gna12 guanine nucleotide binding protein, alpha 12 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20152175 732494 Dscam DS cell adhesion molecule gene MP:0000018 small ears IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:18216855 732494 Dscam DS cell adhesion molecule gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0000440 domed cranium IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:18216855 732494 Dscam DS cell adhesion molecule gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:19945391 732494 Dscam DS cell adhesion molecule gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0001329 retina hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18216855 732494 Dscam DS cell adhesion molecule gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0001512 trunk curl IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:19261893 732494 Dscam DS cell adhesion molecule gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:19261893 732494 Dscam DS cell adhesion molecule gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:19261893 732494 Dscam DS cell adhesion molecule gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:19261893 732494 Dscam DS cell adhesion molecule gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:18216855 732494 Dscam DS cell adhesion molecule gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:19945391 732494 Dscam DS cell adhesion molecule gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19945391 732494 Dscam DS cell adhesion molecule gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18216855 732494 Dscam DS cell adhesion molecule gene MP:0003880 abnormal central pattern generator function IAGP N RGD:5509061 20141003 MGI PMID:19261893 732494 Dscam DS cell adhesion molecule gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18216855 732494 Dscam DS cell adhesion molecule gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22063212 732494 Dscam DS cell adhesion molecule gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19945391 732494 Dscam DS cell adhesion molecule gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0005423 abnormal somatic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:19261893 732494 Dscam DS cell adhesion molecule gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19945391 732494 Dscam DS cell adhesion molecule gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:19261893 732494 Dscam DS cell adhesion molecule gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19945391 732494 Dscam DS cell adhesion molecule gene MP:0006075 abnormal retina cone bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22063212 732494 Dscam DS cell adhesion molecule gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0008105 increased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:22063212 732494 Dscam DS cell adhesion molecule gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0008508 thick retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0008509 disorganized retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:18216855 732494 Dscam DS cell adhesion molecule gene MP:0008509 disorganized retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0008779 abnormal maternal behavior IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:19261893 732494 Dscam DS cell adhesion molecule gene MP:0009393 abnormal resting posture IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:22063212 732494 Dscam DS cell adhesion molecule gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19261893 732494 Dscam DS cell adhesion molecule gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19261893 732494 Dscam DS cell adhesion molecule gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20715164 732494 Dscam DS cell adhesion molecule gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0011996 abnormal retina inner nuclear layer thickness IAGP N RGD:5509061 20141003 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0012008 delayed parturition IAGP N RGD:5509061 20141003 MGI PMID:19261893 732494 Dscam DS cell adhesion molecule gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20160204 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0014265 thick retina inner plexiform layer IAGP N RGD:5509061 20230706 MGI PMID:23300735 732494 Dscam DS cell adhesion molecule gene MP:0030076 abnormal cranial cavity morphology IAGP N RGD:5509061 20170928 MGI PMID:21904980 732494 Dscam DS cell adhesion molecule gene MP:0031442 enlarged cerebral aqueduct IAGP N RGD:5509061 20221103 MGI PMID:21904980 732497 Golph3 golgi phosphoprotein 3 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20210826 MGI 732497 Golph3 golgi phosphoprotein 3 gene MP:0000550 abnormal forelimb morphology IEA N RGD:5509061 20190502 MGI 732497 Golph3 golgi phosphoprotein 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20190502 MGI 732497 Golph3 golgi phosphoprotein 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 732497 Golph3 golgi phosphoprotein 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20190502 MGI 732497 Golph3 golgi phosphoprotein 3 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20190502 MGI 732497 Golph3 golgi phosphoprotein 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20190502 MGI 732497 Golph3 golgi phosphoprotein 3 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20231207 MGI 732497 Golph3 golgi phosphoprotein 3 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 732497 Golph3 golgi phosphoprotein 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 732497 Golph3 golgi phosphoprotein 3 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 732497 Golph3 golgi phosphoprotein 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 732497 Golph3 golgi phosphoprotein 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 732497 Golph3 golgi phosphoprotein 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 732497 Golph3 golgi phosphoprotein 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201022 MGI 732500 Adcy3 adenylate cyclase 3 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:15705663 732500 Adcy3 adenylate cyclase 3 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:12665798 732500 Adcy3 adenylate cyclase 3 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17537788 732500 Adcy3 adenylate cyclase 3 gene MP:0001261 obese IAGP N RGD:5509061 20180712 MGI PMID:19174512 732500 Adcy3 adenylate cyclase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11055432 732500 Adcy3 adenylate cyclase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160128 MGI PMID:25329148 732500 Adcy3 adenylate cyclase 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160128 MGI PMID:25329148 732500 Adcy3 adenylate cyclase 3 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0001433 polyphagia IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0001762 polyuria IAGP N RGD:5509061 20141225 MGI PMID:24431204 732500 Adcy3 adenylate cyclase 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15705663 732500 Adcy3 adenylate cyclase 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15705663 732500 Adcy3 adenylate cyclase 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15705663 732500 Adcy3 adenylate cyclase 3 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:23077041 732500 Adcy3 adenylate cyclase 3 gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:12665798 732500 Adcy3 adenylate cyclase 3 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141225 MGI PMID:24431204 732500 Adcy3 adenylate cyclase 3 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:11055432 732500 Adcy3 adenylate cyclase 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 732500 Adcy3 adenylate cyclase 3 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20210128 MGI 732500 Adcy3 adenylate cyclase 3 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15705663 732500 Adcy3 adenylate cyclase 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20160128 MGI PMID:25329148 732500 Adcy3 adenylate cyclase 3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141225 MGI PMID:24431204 732500 Adcy3 adenylate cyclase 3 gene MP:0003353 decreased circulating renin level IAGP N RGD:5509061 20180712 MGI PMID:19174512 732500 Adcy3 adenylate cyclase 3 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20141003 MGI PMID:15705663 732500 Adcy3 adenylate cyclase 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 732500 Adcy3 adenylate cyclase 3 gene MP:0004512 anosmia IAGP N RGD:5509061 20141003 MGI PMID:11055432 732500 Adcy3 adenylate cyclase 3 gene MP:0004512 anosmia IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17537788 732500 Adcy3 adenylate cyclase 3 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20160128 MGI PMID:25329148 732500 Adcy3 adenylate cyclase 3 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20160128 MGI PMID:25329148 732500 Adcy3 adenylate cyclase 3 gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20180712 MGI PMID:19174512 732500 Adcy3 adenylate cyclase 3 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20180712 MGI PMID:19174512 732500 Adcy3 adenylate cyclase 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20160128 MGI PMID:25329148 732500 Adcy3 adenylate cyclase 3 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 732500 Adcy3 adenylate cyclase 3 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141225 MGI PMID:24431204 732500 Adcy3 adenylate cyclase 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20160128 MGI PMID:25329148 732500 Adcy3 adenylate cyclase 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20160128 MGI PMID:25329148 732500 Adcy3 adenylate cyclase 3 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141225 MGI PMID:24431204 732500 Adcy3 adenylate cyclase 3 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:11055432 732500 Adcy3 adenylate cyclase 3 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20160128 MGI PMID:25329148 732500 Adcy3 adenylate cyclase 3 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20160128 MGI PMID:25329148 732500 Adcy3 adenylate cyclase 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 732500 Adcy3 adenylate cyclase 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20160128 MGI PMID:25329148 732500 Adcy3 adenylate cyclase 3 gene MP:0011085 postnatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 732500 Adcy3 adenylate cyclase 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11055432 732500 Adcy3 adenylate cyclase 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 732500 Adcy3 adenylate cyclase 3 gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20240627 MGI PMID:12665798 732500 Adcy3 adenylate cyclase 3 gene MP:0012287 increased frequency of paradoxical sleep IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0012289 abnormal non-rapid eye movement sleep pattern IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0012460 decreased dentate gyrus size IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0013288 premature acrosome reaction IAGP N RGD:5509061 20191226 MGI PMID:15705663 732500 Adcy3 adenylate cyclase 3 gene MP:0020083 decreased hippocampus volume IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0020478 abnormal circadian sleep/wake cycle IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0021090 abnormal dendrite arborization pattern IAGP N RGD:5509061 20220421 MGI PMID:26868444 732500 Adcy3 adenylate cyclase 3 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:25329148 732500 Adcy3 adenylate cyclase 3 gene MP:0031392 hypoactivity IAGP N RGD:5509061 20220421 MGI PMID:26868444 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000087 absent mandible IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:14622137 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:19017799 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20170629 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20170629 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000705 athymia IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:16226508 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16226508 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20170629 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18596172 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17913910 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:21849556 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:21849556 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:21849556 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21849556 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:21849556 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:21849556 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:21849556 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17913910 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18596172 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17913910 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17913910 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18596172 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:19017799 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17709754 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:19017799 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14502223 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001705 abnormal proximal-distal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:14502223 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:14622137 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:14622137 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0001717 absent ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:14502223 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21514245 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:14502223 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16226508 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:14502223 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0002583 absent extraembryonic ectoderm IAGP N RGD:5509061 20141003 MGI PMID:14502223 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20170629 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:14622137 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:15096454 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:21849556 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15096454 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:14622137 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21849556 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:15096454 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:21849556 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0003808 increased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:19017799 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:16226508 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14622137 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20368360 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20170629 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:16226508 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20170629 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0004594 abnormal mandibular coronoid process morphology IAGP N RGD:5509061 20170629 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20171102 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:16226508 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14502223 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16226508 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16226508 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16226508 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16226508 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15096454 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17709754 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:14502223 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:16226508 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0005432 abnormal pro-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18356083 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20170629 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:18596172 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20368360 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16226508 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16226508 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:18356083 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0008233 abnormal pro-B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18356083 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21514245 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:14622137 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21849556 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21849556 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20170629 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0009905 absent tongue IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20170629 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18596172 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0010283 decreased classified tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21514245 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19017799 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170629 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17913910 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16226508 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14502223 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14622137 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17913910 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19017799 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20150910 MGI PMID:18952847 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14502223 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:14502223 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:14622137 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20368360 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0012056 abnormal polar trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:14502223 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0012269 nuchal edema IAGP N RGD:5509061 20141003 MGI PMID:19017799 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:20368360 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0030026 small Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0030209 abnormal extrinsic tongue muscle morphology IAGP N RGD:5509061 20171026 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0030258 small mandibular condyloid process IAGP N RGD:5509061 20171019 MGI PMID:26395480 732503 Mapk1 mitogen-activated protein kinase 1 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:26395480 732505 Slc25a11 solute carrier family 25 (mitochondrial carrier oxoglutarate carrier), member 11 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20201112 MGI PMID:30686754 732505 Slc25a11 solute carrier family 25 (mitochondrial carrier oxoglutarate carrier), member 11 gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20201112 MGI PMID:30686754 732505 Slc25a11 solute carrier family 25 (mitochondrial carrier oxoglutarate carrier), member 11 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20220203 MGI PMID:28569793 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0001127 small ovary IAGP N RGD:5509061 20220203 MGI PMID:28569793 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220203 MGI PMID:28569793 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12447384 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0001926 female infertility IAGP N RGD:5509061 20220203 MGI PMID:28569793 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12447384 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20160421 MGI 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15471862 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:12447384 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0002544 brachydactyly IEA N RGD:5509061 20160421 MGI 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:12447384 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20220203 MGI PMID:28569793 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:12447384 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23645881 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:12447384 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12447384 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0008869 anovulation IAGP N RGD:5509061 20220203 MGI PMID:28569793 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0009593 absent chorion IAGP N RGD:5509061 20141003 MGI PMID:12447384 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0009706 absent midgut IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20220203 MGI PMID:28569793 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12447384 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12447384 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15471862 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:28569793 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:12447384 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:9811571 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:12447384 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0012737 abnormal primary polar body morphology IAGP N RGD:5509061 20220203 MGI PMID:28569793 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20220203 MGI PMID:28569793 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0031018 decreased granulosa cell proliferation IAGP N RGD:5509061 20220203 MGI PMID:28569793 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220203 MGI PMID:28569793 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0031380 abnormal secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:28569793 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:28569793 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:28569793 732508 Furin furin, paired basic amino acid cleaving enzyme gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220630 MGI PMID:28569793 732510 Ndel1 nudE neurodevelopment protein 1 like 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:16107726 732510 Ndel1 nudE neurodevelopment protein 1 like 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 732510 Ndel1 nudE neurodevelopment protein 1 like 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20181227 MGI 732510 Ndel1 nudE neurodevelopment protein 1 like 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16107726 732510 Ndel1 nudE neurodevelopment protein 1 like 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 732510 Ndel1 nudE neurodevelopment protein 1 like 1 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:16107726 732510 Ndel1 nudE neurodevelopment protein 1 like 1 gene MP:0005388 respiratory system phenotype IEA N RGD:5509061 20181227 MGI 732510 Ndel1 nudE neurodevelopment protein 1 like 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:16107726 732510 Ndel1 nudE neurodevelopment protein 1 like 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16107726 732510 Ndel1 nudE neurodevelopment protein 1 like 1 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16107726 732510 Ndel1 nudE neurodevelopment protein 1 like 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16107726 732510 Ndel1 nudE neurodevelopment protein 1 like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732514 Strn3 striatin, calmodulin binding protein 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 732514 Strn3 striatin, calmodulin binding protein 3 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20191128 MGI 732514 Strn3 striatin, calmodulin binding protein 3 gene MP:0001698 decreased embryo size IEA N RGD:5509061 20191128 MGI 732514 Strn3 striatin, calmodulin binding protein 3 gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20191205 MGI 732514 Strn3 striatin, calmodulin binding protein 3 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 732514 Strn3 striatin, calmodulin binding protein 3 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 732514 Strn3 striatin, calmodulin binding protein 3 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 732514 Strn3 striatin, calmodulin binding protein 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20181227 MGI 732514 Strn3 striatin, calmodulin binding protein 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160421 MGI 732514 Strn3 striatin, calmodulin binding protein 3 gene MP:0009331 absent primitive node IEA N RGD:5509061 20191128 MGI 732514 Strn3 striatin, calmodulin binding protein 3 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 732514 Strn3 striatin, calmodulin binding protein 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732514 Strn3 striatin, calmodulin binding protein 3 gene MP:0012724 absent head fold IEA N RGD:5509061 20191128 MGI 732514 Strn3 striatin, calmodulin binding protein 3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 732514 Strn3 striatin, calmodulin binding protein 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 732516 Tra2b transformer 2 beta gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21803291 732516 Tra2b transformer 2 beta gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:20190275 732516 Tra2b transformer 2 beta gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20190275 732516 Tra2b transformer 2 beta gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:20190275 732516 Tra2b transformer 2 beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20190275 732516 Tra2b transformer 2 beta gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21803291 732516 Tra2b transformer 2 beta gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20190275 732516 Tra2b transformer 2 beta gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21803291 732516 Tra2b transformer 2 beta gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20190275 732519 Prep prolyl endopeptidase gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19564876 732519 Prep prolyl endopeptidase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19564876 732519 Prep prolyl endopeptidase gene MP:0001488 increased startle reflex IEA N RGD:5509061 20141003 MGI 732519 Prep prolyl endopeptidase gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20201022 MGI 732519 Prep prolyl endopeptidase gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19564876 732519 Prep prolyl endopeptidase gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:19564876 732519 Prep prolyl endopeptidase gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:19564876 732519 Prep prolyl endopeptidase gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19564876 732519 Prep prolyl endopeptidase gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20160407 MGI PMID:19564876 732519 Prep prolyl endopeptidase gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20211021 MGI 732519 Prep prolyl endopeptidase gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 732519 Prep prolyl endopeptidase gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19564876 732519 Prep prolyl endopeptidase gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:19564876 732519 Prep prolyl endopeptidase gene MP:0006087 increased body mass index IAGP N RGD:5509061 20141003 MGI PMID:19564876 732519 Prep prolyl endopeptidase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20141003 MGI 732519 Prep prolyl endopeptidase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19564876 732519 Prep prolyl endopeptidase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732519 Prep prolyl endopeptidase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 732519 Prep prolyl endopeptidase gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 732521 Dkk3 dickkopf WNT signaling pathway inhibitor 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16508007 732521 Dkk3 dickkopf WNT signaling pathway inhibitor 3 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16508007 732521 Dkk3 dickkopf WNT signaling pathway inhibitor 3 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:16508007 732521 Dkk3 dickkopf WNT signaling pathway inhibitor 3 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:16508007 732521 Dkk3 dickkopf WNT signaling pathway inhibitor 3 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:22918120 732521 Dkk3 dickkopf WNT signaling pathway inhibitor 3 gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:16508007 732521 Dkk3 dickkopf WNT signaling pathway inhibitor 3 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:16508007 732521 Dkk3 dickkopf WNT signaling pathway inhibitor 3 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:16508007 732523 Tgfb1i1 transforming growth factor beta 1 induced transcript 1 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20171214 MGI PMID:27893716 732523 Tgfb1i1 transforming growth factor beta 1 induced transcript 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26172113 732523 Tgfb1i1 transforming growth factor beta 1 induced transcript 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20160505 MGI PMID:20933520 732523 Tgfb1i1 transforming growth factor beta 1 induced transcript 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20170105 MGI 732523 Tgfb1i1 transforming growth factor beta 1 induced transcript 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20160421 MGI 732523 Tgfb1i1 transforming growth factor beta 1 induced transcript 1 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20160505 MGI PMID:20933520 732523 Tgfb1i1 transforming growth factor beta 1 induced transcript 1 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20171214 MGI PMID:27893716 732523 Tgfb1i1 transforming growth factor beta 1 induced transcript 1 gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20171214 MGI PMID:27893716 732525 Cysltr1 cysteinyl leukotriene receptor 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:23504326 732525 Cysltr1 cysteinyl leukotriene receptor 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 732525 Cysltr1 cysteinyl leukotriene receptor 1 gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:14970333 732525 Cysltr1 cysteinyl leukotriene receptor 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 732525 Cysltr1 cysteinyl leukotriene receptor 1 gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:11932261 732525 Cysltr1 cysteinyl leukotriene receptor 1 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11932261 732525 Cysltr1 cysteinyl leukotriene receptor 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11932261 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17703191 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:18239685 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17703191 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18239685 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0002148 abnormal hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18239685 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18239685 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18239685 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:18239685 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:18239685 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17703191 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:18239685 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18239685 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:18239685 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:18239685 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:18239685 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17703191 732526 Tax1bp1 Tax1 (human T cell leukemia virus type I) binding protein 1 gene MP:0031118 cardiovalvulitis IAGP N RGD:5509061 20200910 MGI PMID:18239685 732528 Nat2 N-acetyltransferase 2 (arylamine N-acetyltransferase) gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:17487534 732528 Nat2 N-acetyltransferase 2 (arylamine N-acetyltransferase) gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17487534 732528 Nat2 N-acetyltransferase 2 (arylamine N-acetyltransferase) gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:17487534 732528 Nat2 N-acetyltransferase 2 (arylamine N-acetyltransferase) gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:17487534 732528 Nat2 N-acetyltransferase 2 (arylamine N-acetyltransferase) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12815365 732528 Nat2 N-acetyltransferase 2 (arylamine N-acetyltransferase) gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:17487534 732528 Nat2 N-acetyltransferase 2 (arylamine N-acetyltransferase) gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:17961509 732528 Nat2 N-acetyltransferase 2 (arylamine N-acetyltransferase) gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:12815365 732528 Nat2 N-acetyltransferase 2 (arylamine N-acetyltransferase) gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:17961509 732528 Nat2 N-acetyltransferase 2 (arylamine N-acetyltransferase) gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:17961509 732529 Trhr2 thyrotropin releasing hormone receptor 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20240404 MGI PMID:19078951 732529 Trhr2 thyrotropin releasing hormone receptor 2 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20240404 MGI PMID:19078951 732532 Fat1 FAT atypical cadherin 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:12724416 732532 Fat1 FAT atypical cadherin 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:12724416 732532 Fat1 FAT atypical cadherin 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20180628 MGI PMID:26905694 732532 Fat1 FAT atypical cadherin 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20180628 MGI PMID:26905694 732532 Fat1 FAT atypical cadherin 1 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:12724416 732532 Fat1 FAT atypical cadherin 1 gene MP:0003099 retina detachment IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0004038 lymphangiectasis IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:12724416 732532 Fat1 FAT atypical cadherin 1 gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:12724416 732532 Fat1 FAT atypical cadherin 1 gene MP:0005261 aniridia IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20180628 MGI PMID:26905694 732532 Fat1 FAT atypical cadherin 1 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20180628 MGI PMID:26905694 732532 Fat1 FAT atypical cadherin 1 gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20141003 MGI PMID:12724416 732532 Fat1 FAT atypical cadherin 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12724416 732532 Fat1 FAT atypical cadherin 1 gene MP:0006290 proboscis IAGP N RGD:5509061 20141003 MGI PMID:12724416 732532 Fat1 FAT atypical cadherin 1 gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20180628 MGI PMID:26905694 732532 Fat1 FAT atypical cadherin 1 gene MP:0008062 abnormal podocyte slit junction morphology IAGP N RGD:5509061 20141003 MGI PMID:12724416 732532 Fat1 FAT atypical cadherin 1 gene MP:0008065 short endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:12724416 732532 Fat1 FAT atypical cadherin 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20180628 MGI PMID:26905694 732532 Fat1 FAT atypical cadherin 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0010056 ectopic skeletal muscle IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0010452 retina microaneurysm IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12724416 732532 Fat1 FAT atypical cadherin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11431694 732532 Fat1 FAT atypical cadherin 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23785297 732532 Fat1 FAT atypical cadherin 1 gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20180628 MGI PMID:26905694 732532 Fat1 FAT atypical cadherin 1 gene MP:0011868 podocyte microvillus transformation IAGP N RGD:5509061 20180628 MGI PMID:26905694 732532 Fat1 FAT atypical cadherin 1 gene MP:0030039 abnormal facial muscle morphology IAGP N RGD:5509061 20170914 MGI PMID:23785297 732534 Dnaja2 DnaJ heat shock protein family (Hsp40) member A2 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 732534 Dnaja2 DnaJ heat shock protein family (Hsp40) member A2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 732534 Dnaja2 DnaJ heat shock protein family (Hsp40) member A2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0001785 edema IEA N RGD:5509061 20170504 MGI 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0010530 cerebral arteriovenous malformation IEA N RGD:5509061 20170504 MGI 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0010912 herniated liver IEA N RGD:5509061 20170504 MGI 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0011493 double ureter IEA N RGD:5509061 20170504 MGI 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0012303 umbilical vein stenosis IEA N RGD:5509061 20170504 MGI 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0013842 ductus venosus stenosis IEA N RGD:5509061 20170504 MGI 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0013847 retropleural edema IEA N RGD:5509061 20170504 MGI 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0013851 abnormal Wolffian duct topology IEA N RGD:5509061 20170504 MGI 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0013865 abnormal dorsal pancreas topology IEA N RGD:5509061 20170504 MGI 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0013963 jugular vein stenosis IEA N RGD:5509061 20170504 MGI 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0013968 multiple persisting craniopharyngeal ducts IEA N RGD:5509061 20170504 MGI 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20170504 MGI 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0014019 embryo cyst IEA N RGD:5509061 20170504 MGI 732536 Slc25a20 solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:29539633 732539 Bid BH3 interacting domain death agonist gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:12934064 732539 Bid BH3 interacting domain death agonist gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17096024 732539 Bid BH3 interacting domain death agonist gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:16780816 732539 Bid BH3 interacting domain death agonist gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12668632 732539 Bid BH3 interacting domain death agonist gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12754217 732539 Bid BH3 interacting domain death agonist gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:12934064 732539 Bid BH3 interacting domain death agonist gene MP:0001316 cornea scarring IAGP N RGD:5509061 20141003 MGI PMID:12934064 732539 Bid BH3 interacting domain death agonist gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12934064 732539 Bid BH3 interacting domain death agonist gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:12934064 732539 Bid BH3 interacting domain death agonist gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:16780816 732539 Bid BH3 interacting domain death agonist gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16537427 732539 Bid BH3 interacting domain death agonist gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17096024 732539 Bid BH3 interacting domain death agonist gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:22446738 732539 Bid BH3 interacting domain death agonist gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12934064 732539 Bid BH3 interacting domain death agonist gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:12934064 732539 Bid BH3 interacting domain death agonist gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:10476969 732539 Bid BH3 interacting domain death agonist gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:17448999 732539 Bid BH3 interacting domain death agonist gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16873683 732539 Bid BH3 interacting domain death agonist gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:10476969 732539 Bid BH3 interacting domain death agonist gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10476969 732539 Bid BH3 interacting domain death agonist gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17101783 732539 Bid BH3 interacting domain death agonist gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22446738 732539 Bid BH3 interacting domain death agonist gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10476969 732539 Bid BH3 interacting domain death agonist gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12754217 732539 Bid BH3 interacting domain death agonist gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17448999 732539 Bid BH3 interacting domain death agonist gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22446738 732539 Bid BH3 interacting domain death agonist gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17101783 732539 Bid BH3 interacting domain death agonist gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17101783 732540 Dbnl drebrin-like gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20200514 MGI 732540 Dbnl drebrin-like gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210826 MGI 732540 Dbnl drebrin-like gene MP:0000420 ruffled hair IAGP N RGD:5509061 20180531 MGI PMID:16601697 732540 Dbnl drebrin-like gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16055701 732540 Dbnl drebrin-like gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16601697 732540 Dbnl drebrin-like gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:16055701 732540 Dbnl drebrin-like gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:16601697 732540 Dbnl drebrin-like gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:16601697 732540 Dbnl drebrin-like gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:16601697 732540 Dbnl drebrin-like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16055701 732540 Dbnl drebrin-like gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16601697 732540 Dbnl drebrin-like gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210128 MGI 732540 Dbnl drebrin-like gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 732540 Dbnl drebrin-like gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16601697 732540 Dbnl drebrin-like gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 732540 Dbnl drebrin-like gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16601697 732540 Dbnl drebrin-like gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:16601697 732540 Dbnl drebrin-like gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16601697 732540 Dbnl drebrin-like gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16055701 732540 Dbnl drebrin-like gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:16055701 732540 Dbnl drebrin-like gene MP:0001954 respiratory distress IAGP N RGD:5509061 20180531 MGI PMID:16601697 732540 Dbnl drebrin-like gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:16601697 732540 Dbnl drebrin-like gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:16601697 732540 Dbnl drebrin-like gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16055701 732540 Dbnl drebrin-like gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16055701 732540 Dbnl drebrin-like gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210826 MGI 732540 Dbnl drebrin-like gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 732540 Dbnl drebrin-like gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20210128 MGI 732540 Dbnl drebrin-like gene MP:0002833 increased heart weight IEA N RGD:5509061 20200514 MGI 732540 Dbnl drebrin-like gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210826 MGI 732540 Dbnl drebrin-like gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210826 MGI 732540 Dbnl drebrin-like gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 732540 Dbnl drebrin-like gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20211021 MGI 732540 Dbnl drebrin-like gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 732540 Dbnl drebrin-like gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:16601697 732540 Dbnl drebrin-like gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16601697 732540 Dbnl drebrin-like gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16055701 732540 Dbnl drebrin-like gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20200514 MGI 732540 Dbnl drebrin-like gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20200514 MGI 732540 Dbnl drebrin-like gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20200514 MGI 732540 Dbnl drebrin-like gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210826 MGI 732540 Dbnl drebrin-like gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20200514 MGI 732540 Dbnl drebrin-like gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20210128 MGI 732540 Dbnl drebrin-like gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16055701 732540 Dbnl drebrin-like gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:16055701 732540 Dbnl drebrin-like gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 732540 Dbnl drebrin-like gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20210128 MGI 732540 Dbnl drebrin-like gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16055701 732540 Dbnl drebrin-like gene MP:0011941 increased fluid intake IEA N RGD:5509061 20211021 MGI 732540 Dbnl drebrin-like gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 732540 Dbnl drebrin-like gene MP:0013807 generalized edema IAGP N RGD:5509061 20180531 MGI PMID:16601697 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:12101250 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0000155 asymmetric rib joints IAGP N RGD:5509061 20141003 MGI PMID:12101250 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21124733 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:12101250 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21124733 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23059197 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23059197 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:12101250 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23059197 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:23059197 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12101250 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23059197 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:21124733 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12101250 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23059197 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23059197 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12101250 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:12101250 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:21124733 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:23059197 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12101250 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21124733 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12101250 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:12101250 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:12101250 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:12101250 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23059197 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0008896 increased IgG2c level IAGP N RGD:5509061 20141003 MGI PMID:18513163 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23059197 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:21124733 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:21124733 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:21124733 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21124733 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:23059197 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12101250 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0012109 decreased trophoblast glycogen cell number IAGP N RGD:5509061 20141003 MGI PMID:23059197 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:21124733 732543 Dlk1 delta like non-canonical Notch ligand 1 gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:21124733 732544 Pi4k2a phosphatidylinositol 4-kinase type 2 alpha gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19581584 732544 Pi4k2a phosphatidylinositol 4-kinase type 2 alpha gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:19581584 732544 Pi4k2a phosphatidylinositol 4-kinase type 2 alpha gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:19581584 732544 Pi4k2a phosphatidylinositol 4-kinase type 2 alpha gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19581584 732544 Pi4k2a phosphatidylinositol 4-kinase type 2 alpha gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19581584 732544 Pi4k2a phosphatidylinositol 4-kinase type 2 alpha gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:19581584 732544 Pi4k2a phosphatidylinositol 4-kinase type 2 alpha gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:19581584 732544 Pi4k2a phosphatidylinositol 4-kinase type 2 alpha gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19581584 732544 Pi4k2a phosphatidylinositol 4-kinase type 2 alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19581584 732544 Pi4k2a phosphatidylinositol 4-kinase type 2 alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19581584 732544 Pi4k2a phosphatidylinositol 4-kinase type 2 alpha gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:19581584 732544 Pi4k2a phosphatidylinositol 4-kinase type 2 alpha gene MP:0003280 urinary incontinence IAGP N RGD:5509061 20141003 MGI PMID:19581584 732544 Pi4k2a phosphatidylinositol 4-kinase type 2 alpha gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:19581584 732544 Pi4k2a phosphatidylinositol 4-kinase type 2 alpha gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19581584 732544 Pi4k2a phosphatidylinositol 4-kinase type 2 alpha gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19581584 732546 Mafb MAF bZIP transcription factor B gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:14207033 732546 Mafb MAF bZIP transcription factor B gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:14207033 732546 Mafb MAF bZIP transcription factor B gene MP:0000041 absent endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:4758758 732546 Mafb MAF bZIP transcription factor B gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:16847325 732546 Mafb MAF bZIP transcription factor B gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:24327562 732546 Mafb MAF bZIP transcription factor B gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16847325 732546 Mafb MAF bZIP transcription factor B gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20190228 MGI PMID:27181683 732546 Mafb MAF bZIP transcription factor B gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:8100767 732546 Mafb MAF bZIP transcription factor B gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20190228 MGI PMID:27181683 732546 Mafb MAF bZIP transcription factor B gene MP:0001061 abnormal oculomotor nerve morphology IAGP N RGD:5509061 20190228 MGI PMID:27181683 732546 Mafb MAF bZIP transcription factor B gene MP:0001070 abnormal abducens nerve morphology IAGP N RGD:5509061 20190228 MGI PMID:27181683 732546 Mafb MAF bZIP transcription factor B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200409 MGI PMID:30369533 732546 Mafb MAF bZIP transcription factor B gene MP:0001394 circling IEA N RGD:5509061 20111116 MGI 732546 Mafb MAF bZIP transcription factor B gene MP:0001399 hyperactivity IEA N RGD:5509061 20111116 MGI 732546 Mafb MAF bZIP transcription factor B gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:14513037 732546 Mafb MAF bZIP transcription factor B gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:24327562 732546 Mafb MAF bZIP transcription factor B gene MP:0001922 reduced male fertility IEA N RGD:5509061 20111116 MGI 732546 Mafb MAF bZIP transcription factor B gene MP:0001923 reduced female fertility IEA N RGD:5509061 20111116 MGI 732546 Mafb MAF bZIP transcription factor B gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:14513037 732546 Mafb MAF bZIP transcription factor B gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:14513037 732546 Mafb MAF bZIP transcription factor B gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:14513037 732546 Mafb MAF bZIP transcription factor B gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:14513037 732546 Mafb MAF bZIP transcription factor B gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:24327562 732546 Mafb MAF bZIP transcription factor B gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:14513037 732546 Mafb MAF bZIP transcription factor B gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:24327562 732546 Mafb MAF bZIP transcription factor B gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16847325 732546 Mafb MAF bZIP transcription factor B gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:14207033 732546 Mafb MAF bZIP transcription factor B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24327562 732546 Mafb MAF bZIP transcription factor B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201210 MGI PMID:29779709 732546 Mafb MAF bZIP transcription factor B gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:4758758 732546 Mafb MAF bZIP transcription factor B gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16847325 732546 Mafb MAF bZIP transcription factor B gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20200409 MGI PMID:30369533 732546 Mafb MAF bZIP transcription factor B gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:24327562 732546 Mafb MAF bZIP transcription factor B gene MP:0002959 increased urine microalbumin level IAGP N RGD:5509061 20200409 MGI PMID:30369533 732546 Mafb MAF bZIP transcription factor B gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:4758758 732546 Mafb MAF bZIP transcription factor B gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14207033 732546 Mafb MAF bZIP transcription factor B gene MP:0003624 anuria IAGP N RGD:5509061 20141003 MGI PMID:16847325 732546 Mafb MAF bZIP transcription factor B gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:14513037 732546 Mafb MAF bZIP transcription factor B gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:4758758 732546 Mafb MAF bZIP transcription factor B gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16847325 732546 Mafb MAF bZIP transcription factor B gene MP:0004289 abnormal bony labyrinth IAGP N RGD:5509061 20141003 MGI PMID:14207033 732546 Mafb MAF bZIP transcription factor B gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:16847325 732546 Mafb MAF bZIP transcription factor B gene MP:0004562 abnormal inner hair cell synaptic ribbon morphology IAGP N RGD:5509061 20141003 MGI PMID:24327562 732546 Mafb MAF bZIP transcription factor B gene MP:0004568 fusion of glossopharyngeal and vagus nerve IAGP N RGD:5509061 20190228 MGI PMID:27181683 732546 Mafb MAF bZIP transcription factor B gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20200409 MGI PMID:30369533 732546 Mafb MAF bZIP transcription factor B gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:14513037 732546 Mafb MAF bZIP transcription factor B gene MP:0005307 head tossing IEA N RGD:5509061 20111116 MGI 732546 Mafb MAF bZIP transcription factor B gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20201210 MGI PMID:29779709 732546 Mafb MAF bZIP transcription factor B gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20201210 MGI PMID:29779709 732546 Mafb MAF bZIP transcription factor B gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16847325 732546 Mafb MAF bZIP transcription factor B gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:4758758 732546 Mafb MAF bZIP transcription factor B gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:14207033 732546 Mafb MAF bZIP transcription factor B gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:4758758 732546 Mafb MAF bZIP transcription factor B gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20111116 MGI 732546 Mafb MAF bZIP transcription factor B gene MP:0006287 inner ear cyst IAGP N RGD:5509061 20141003 MGI PMID:16847325 732546 Mafb MAF bZIP transcription factor B gene MP:0006287 inner ear cyst IAGP N RGD:5509061 20141003 MGI PMID:24327562 732546 Mafb MAF bZIP transcription factor B gene MP:0006287 inner ear cyst IAGP N RGD:5509061 20141003 MGI PMID:4758758 732546 Mafb MAF bZIP transcription factor B gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20201210 MGI PMID:29779709 732546 Mafb MAF bZIP transcription factor B gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:16847325 732546 Mafb MAF bZIP transcription factor B gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20200409 MGI PMID:30369533 732546 Mafb MAF bZIP transcription factor B gene MP:0009913 abnormal hyoid bone greater horn morphology IAGP N RGD:5509061 20141003 MGI PMID:8100767 732546 Mafb MAF bZIP transcription factor B gene MP:0010395 abnormal pharyngeal arch development IAGP N RGD:5509061 20141003 MGI PMID:8100767 732546 Mafb MAF bZIP transcription factor B gene MP:0010396 ectopic pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:8100767 732546 Mafb MAF bZIP transcription factor B gene MP:0010397 abnormal otic capsule development IAGP N RGD:5509061 20141003 MGI PMID:14207033 732546 Mafb MAF bZIP transcription factor B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20201210 MGI PMID:29779709 732546 Mafb MAF bZIP transcription factor B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16847325 732546 Mafb MAF bZIP transcription factor B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24327562 732546 Mafb MAF bZIP transcription factor B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20220407 MGI PMID:33715275 732546 Mafb MAF bZIP transcription factor B gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14513037 732546 Mafb MAF bZIP transcription factor B gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20201210 MGI PMID:29779709 732546 Mafb MAF bZIP transcription factor B gene MP:0011868 podocyte microvillus transformation IAGP N RGD:5509061 20200409 MGI PMID:30369533 732546 Mafb MAF bZIP transcription factor B gene MP:0011932 abnormal endocrine pancreas development IAGP N RGD:5509061 20141003 MGI PMID:18199433 732546 Mafb MAF bZIP transcription factor B gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:24327562 732546 Mafb MAF bZIP transcription factor B gene MP:0012796 abnormal rhombomere 4 morphology IAGP N RGD:5509061 20141003 MGI PMID:14207033 732546 Mafb MAF bZIP transcription factor B gene MP:0012800 abnormal rhombomere 5 morphology IEA N RGD:5509061 20141003 MGI 732546 Mafb MAF bZIP transcription factor B gene MP:0013849 absent abducens nerve IAGP N RGD:5509061 20190228 MGI PMID:27181683 732546 Mafb MAF bZIP transcription factor B gene MP:0014167 ectopic bone IAGP N RGD:5509061 20160407 MGI PMID:8100767 732548 Msn moesin gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20220811 MGI 732548 Msn moesin gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220811 MGI 732548 Msn moesin gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20190221 MGI PMID:22875842 732548 Msn moesin gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20190221 MGI PMID:18658275 732548 Msn moesin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9890997 732548 Msn moesin gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 732548 Msn moesin gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 732548 Msn moesin gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20220811 MGI 732548 Msn moesin gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 732548 Msn moesin gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 732548 Msn moesin gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20190221 MGI PMID:22875842 732548 Msn moesin gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20190221 MGI PMID:22875842 732548 Msn moesin gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20190221 MGI PMID:22875842 732548 Msn moesin gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20190221 MGI PMID:18658275 732548 Msn moesin gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 732548 Msn moesin gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20201022 MGI 732548 Msn moesin gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190221 MGI PMID:22875842 732548 Msn moesin gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20190221 MGI PMID:18658275 732548 Msn moesin gene MP:0020212 impaired leukocyte migration IAGP N RGD:5509061 20190221 MGI PMID:22875842 732550 Tex101 testis expressed gene 101 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23633567 732550 Tex101 testis expressed gene 101 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23969891 732550 Tex101 testis expressed gene 101 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220811 MGI 732550 Tex101 testis expressed gene 101 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220811 MGI 732550 Tex101 testis expressed gene 101 gene MP:0009281 abnormal hyperactivated sperm motility IAGP N RGD:5509061 20220303 MGI PMID:23633567 732550 Tex101 testis expressed gene 101 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:23969891 732550 Tex101 testis expressed gene 101 gene MP:0013287 abnormal acrosome reaction IAGP N RGD:5509061 20220303 MGI PMID:23633567 732550 Tex101 testis expressed gene 101 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20200102 MGI PMID:23969891 732550 Tex101 testis expressed gene 101 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20220303 MGI PMID:23633567 732550 Tex101 testis expressed gene 101 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220303 MGI PMID:23633567 732550 Tex101 testis expressed gene 101 gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20220303 MGI PMID:23969891 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0003509 increased circulating dihydrotestosterone level IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0008938 decreased pituitary gland weight IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0008940 delayed balanopreputial separation IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0009819 abnormal circulating androgen level IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0011384 abnormal progesterone level IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0013602 abnormal Leydig cell differentiation IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20210318 MGI PMID:32190925 732551 Hsd17b3 hydroxysteroid (17-beta) dehydrogenase 3 gene MP:0031362 decreased prostate gland ventral lobe weight IAGP N RGD:5509061 20220303 MGI PMID:32190925 732552 Sult1d1 sulfotransferase family 1D, member 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20150219 MGI PMID:24802129 732552 Sult1d1 sulfotransferase family 1D, member 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20150219 MGI PMID:24802129 732556 Mipep mitochondrial intermediate peptidase gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220811 MGI 732556 Mipep mitochondrial intermediate peptidase gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 732556 Mipep mitochondrial intermediate peptidase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732556 Mipep mitochondrial intermediate peptidase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 732558 Vdac1 voltage-dependent anion channel 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11907043 732558 Vdac1 voltage-dependent anion channel 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11907043 732558 Vdac1 voltage-dependent anion channel 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11907043 732558 Vdac1 voltage-dependent anion channel 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11907043 732558 Vdac1 voltage-dependent anion channel 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20190502 MGI 732558 Vdac1 voltage-dependent anion channel 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11907043 732558 Vdac1 voltage-dependent anion channel 1 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:11907043 732558 Vdac1 voltage-dependent anion channel 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 732558 Vdac1 voltage-dependent anion channel 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11907043 732558 Vdac1 voltage-dependent anion channel 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11907043 732558 Vdac1 voltage-dependent anion channel 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 732560 Prelp proline arginine-rich end leucine-rich repeat gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 732560 Prelp proline arginine-rich end leucine-rich repeat gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 732560 Prelp proline arginine-rich end leucine-rich repeat gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20210128 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9664685 732562 Bmp6 bone morphogenetic protein 6 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:9664685 732562 Bmp6 bone morphogenetic protein 6 gene MP:0000160 kyphosis IEA N RGD:5509061 20210826 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0000613 abnormal salivary gland morphology IEA N RGD:5509061 20220519 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0001258 decreased body length IEA N RGD:5509061 20111116 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0001262 decreased body weight IEA N RGD:5509061 20111116 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210826 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20220519 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9664685 732562 Bmp6 bone morphogenetic protein 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9664685 732562 Bmp6 bone morphogenetic protein 6 gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20220519 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20220519 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210826 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220519 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20210826 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:9664685 732562 Bmp6 bone morphogenetic protein 6 gene MP:0004680 small xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:9664685 732562 Bmp6 bone morphogenetic protein 6 gene MP:0005238 increased brain size IEA N RGD:5509061 20220519 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20220519 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220519 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210826 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20220519 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 732562 Bmp6 bone morphogenetic protein 6 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:9664685 732562 Bmp6 bone morphogenetic protein 6 gene MP:0008785 abnormal sternum manubrium morphology IAGP N RGD:5509061 20141003 MGI PMID:9664685 732562 Bmp6 bone morphogenetic protein 6 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20220519 MGI 732564 Gja8 gap junction protein, alpha 8 gene MP:0001260 increased body weight IAGP N RGD:5509061 20200910 MGI PMID:15253273 732564 Gja8 gap junction protein, alpha 8 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:11786642 732564 Gja8 gap junction protein, alpha 8 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:9813099 732564 Gja8 gap junction protein, alpha 8 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11786642 732564 Gja8 gap junction protein, alpha 8 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11875045 732564 Gja8 gap junction protein, alpha 8 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:1399425 732564 Gja8 gap junction protein, alpha 8 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:16332269 732564 Gja8 gap junction protein, alpha 8 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:16611690 732564 Gja8 gap junction protein, alpha 8 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:23300808 732564 Gja8 gap junction protein, alpha 8 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:9813099 732564 Gja8 gap junction protein, alpha 8 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20190815 MGI PMID:30991053 732564 Gja8 gap junction protein, alpha 8 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200910 MGI PMID:15253273 732564 Gja8 gap junction protein, alpha 8 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:11696604 732564 Gja8 gap junction protein, alpha 8 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:16611690 732564 Gja8 gap junction protein, alpha 8 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20171221 MGI PMID:20844585 732564 Gja8 gap junction protein, alpha 8 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:11696604 732564 Gja8 gap junction protein, alpha 8 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:11846517 732564 Gja8 gap junction protein, alpha 8 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:11875045 732564 Gja8 gap junction protein, alpha 8 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:1399425 732564 Gja8 gap junction protein, alpha 8 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:16332269 732564 Gja8 gap junction protein, alpha 8 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:16611690 732564 Gja8 gap junction protein, alpha 8 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:9813099 732564 Gja8 gap junction protein, alpha 8 gene MP:0001304 cataract IAGP N RGD:5509061 20200910 MGI PMID:15253273 732564 Gja8 gap junction protein, alpha 8 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:11786642 732564 Gja8 gap junction protein, alpha 8 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:11846517 732564 Gja8 gap junction protein, alpha 8 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:23300808 732564 Gja8 gap junction protein, alpha 8 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:9813099 732564 Gja8 gap junction protein, alpha 8 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20190815 MGI PMID:30991053 732564 Gja8 gap junction protein, alpha 8 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20200910 MGI PMID:15253273 732564 Gja8 gap junction protein, alpha 8 gene MP:0001317 abnormal pupil morphology IAGP N RGD:5509061 20200910 MGI PMID:15253273 732564 Gja8 gap junction protein, alpha 8 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20200910 MGI PMID:15253273 732564 Gja8 gap junction protein, alpha 8 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20190815 MGI PMID:30991053 732564 Gja8 gap junction protein, alpha 8 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200910 MGI PMID:15253273 732564 Gja8 gap junction protein, alpha 8 gene MP:0001329 retina hyperplasia IAGP N RGD:5509061 20190815 MGI PMID:30991053 732564 Gja8 gap junction protein, alpha 8 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20190815 MGI PMID:30991053 732564 Gja8 gap junction protein, alpha 8 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:9813099 732564 Gja8 gap junction protein, alpha 8 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20190815 MGI PMID:30991053 732564 Gja8 gap junction protein, alpha 8 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11846517 732564 Gja8 gap junction protein, alpha 8 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11875045 732564 Gja8 gap junction protein, alpha 8 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16611690 732564 Gja8 gap junction protein, alpha 8 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23300808 732564 Gja8 gap junction protein, alpha 8 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9813099 732564 Gja8 gap junction protein, alpha 8 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20200910 MGI PMID:15253273 732564 Gja8 gap junction protein, alpha 8 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 732564 Gja8 gap junction protein, alpha 8 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20200910 MGI PMID:15253273 732564 Gja8 gap junction protein, alpha 8 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:11696604 732564 Gja8 gap junction protein, alpha 8 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20190815 MGI PMID:30991053 732564 Gja8 gap junction protein, alpha 8 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:11786642 732564 Gja8 gap junction protein, alpha 8 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:11875045 732564 Gja8 gap junction protein, alpha 8 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:9813099 732564 Gja8 gap junction protein, alpha 8 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20190815 MGI PMID:30991053 732564 Gja8 gap junction protein, alpha 8 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11696604 732564 Gja8 gap junction protein, alpha 8 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20190815 MGI PMID:30991053 732564 Gja8 gap junction protein, alpha 8 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 732564 Gja8 gap junction protein, alpha 8 gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20141003 MGI PMID:11875045 732564 Gja8 gap junction protein, alpha 8 gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20141003 MGI PMID:16611690 732564 Gja8 gap junction protein, alpha 8 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:1399425 732564 Gja8 gap junction protein, alpha 8 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:16611690 732564 Gja8 gap junction protein, alpha 8 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:23300808 732564 Gja8 gap junction protein, alpha 8 gene MP:0010263 total cataract IAGP N RGD:5509061 20141003 MGI PMID:16611690 732564 Gja8 gap junction protein, alpha 8 gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:16611690 732564 Gja8 gap junction protein, alpha 8 gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:23300808 732564 Gja8 gap junction protein, alpha 8 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20190815 MGI PMID:30991053 732564 Gja8 gap junction protein, alpha 8 gene MP:0031206 hypolipidemia IAGP N RGD:5509061 20210211 MGI PMID:30991053 732564 Gja8 gap junction protein, alpha 8 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:30991053 732565 Lifr LIF receptor alpha gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:7789261 732565 Lifr LIF receptor alpha gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20171214 MGI PMID:28334964 732565 Lifr LIF receptor alpha gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20171214 MGI PMID:28334964 732565 Lifr LIF receptor alpha gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20171214 MGI PMID:28334964 732565 Lifr LIF receptor alpha gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20171214 MGI PMID:28334964 732565 Lifr LIF receptor alpha gene MP:0000536 hydroureter IAGP N RGD:5509061 20171214 MGI PMID:28334964 732565 Lifr LIF receptor alpha gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:7501019 732565 Lifr LIF receptor alpha gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:7789261 732565 Lifr LIF receptor alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7501019 732565 Lifr LIF receptor alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7789261 732565 Lifr LIF receptor alpha gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 732565 Lifr LIF receptor alpha gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:7789261 732565 Lifr LIF receptor alpha gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20171214 MGI PMID:28334964 732565 Lifr LIF receptor alpha gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20160811 MGI 732565 Lifr LIF receptor alpha gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7789261 732565 Lifr LIF receptor alpha gene MP:0002286 cryptorchism IAGP N RGD:5509061 20171214 MGI PMID:28334964 732565 Lifr LIF receptor alpha gene MP:0002989 small kidney IAGP N RGD:5509061 20171214 MGI PMID:28334964 732565 Lifr LIF receptor alpha gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7789261 732565 Lifr LIF receptor alpha gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20171214 MGI PMID:28334964 732565 Lifr LIF receptor alpha gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7789261 732565 Lifr LIF receptor alpha gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20171214 MGI PMID:28334964 732565 Lifr LIF receptor alpha gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20171214 MGI PMID:28334964 732565 Lifr LIF receptor alpha gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:7789261 732565 Lifr LIF receptor alpha gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:7789261 732565 Lifr LIF receptor alpha gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:7789261 732565 Lifr LIF receptor alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7501019 732565 Lifr LIF receptor alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7789261 732565 Lifr LIF receptor alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732565 Lifr LIF receptor alpha gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20171214 MGI PMID:28334964 732565 Lifr LIF receptor alpha gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7789261 732565 Lifr LIF receptor alpha gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20171214 MGI PMID:28334964 732565 Lifr LIF receptor alpha gene MP:0011426 abnormal ureter smooth muscle morphology IAGP N RGD:5509061 20171214 MGI PMID:28334964 732565 Lifr LIF receptor alpha gene MP:0011486 ectopic ureter IAGP N RGD:5509061 20171214 MGI PMID:28334964 732565 Lifr LIF receptor alpha gene MP:0011797 blind ureter IAGP N RGD:5509061 20171214 MGI PMID:28334964 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0000240 extramedullary hematopoiesis IEA N RGD:5509061 20111116 MGI 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20111116 MGI 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0000708 thymus hyperplasia IEA N RGD:5509061 20111116 MGI 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:16505142 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:17277129 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0001836 abnormal antigen presentation via MHC class I IAGP N RGD:5509061 20141003 MGI PMID:16299505 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0001836 abnormal antigen presentation via MHC class I IAGP N RGD:5509061 20141003 MGI PMID:17128277 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0001840 increased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:16505142 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:16299505 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:16505142 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:16754858 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:17277129 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17128277 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20111116 MGI 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16505142 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20211021 MGI 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16299505 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16505142 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17128277 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17277129 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16754858 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17277129 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17277129 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20231207 MGI 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17277129 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230601 MGI 732567 Erap1 endoplasmic reticulum aminopeptidase 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 732570 Mfn2 mitofusin 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22859504 732570 Mfn2 mitofusin 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22619176 732570 Mfn2 mitofusin 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0001147 small testis IAGP N RGD:5509061 20220811 MGI PMID:35493072 732570 Mfn2 mitofusin 2 gene MP:0001147 small testis IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20220811 MGI PMID:35493072 732570 Mfn2 mitofusin 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22859504 732570 Mfn2 mitofusin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22859504 732570 Mfn2 mitofusin 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20240926 MGI PMID:31675497 732570 Mfn2 mitofusin 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22859504 732570 Mfn2 mitofusin 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:22859504 732570 Mfn2 mitofusin 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12527753 732570 Mfn2 mitofusin 2 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:12527753 732570 Mfn2 mitofusin 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12527753 732570 Mfn2 mitofusin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22859504 732570 Mfn2 mitofusin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:22859504 732570 Mfn2 mitofusin 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22859504 732570 Mfn2 mitofusin 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:22859504 732570 Mfn2 mitofusin 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20240926 MGI PMID:31675497 732570 Mfn2 mitofusin 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22859504 732570 Mfn2 mitofusin 2 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:22859504 732570 Mfn2 mitofusin 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 732570 Mfn2 mitofusin 2 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:22859504 732570 Mfn2 mitofusin 2 gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:22619176 732570 Mfn2 mitofusin 2 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:22619176 732570 Mfn2 mitofusin 2 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:20335458 732570 Mfn2 mitofusin 2 gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:22859504 732570 Mfn2 mitofusin 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0004930 small epididymis IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12527753 732570 Mfn2 mitofusin 2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:22859504 732570 Mfn2 mitofusin 2 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20220811 MGI PMID:35493072 732570 Mfn2 mitofusin 2 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20240926 MGI PMID:31675497 732570 Mfn2 mitofusin 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22619176 732570 Mfn2 mitofusin 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:12527753 732570 Mfn2 mitofusin 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:17296794 732570 Mfn2 mitofusin 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:22619176 732570 Mfn2 mitofusin 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:22859504 732570 Mfn2 mitofusin 2 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:12527753 732570 Mfn2 mitofusin 2 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:20335458 732570 Mfn2 mitofusin 2 gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:22619176 732570 Mfn2 mitofusin 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20141003 MGI PMID:22619176 732570 Mfn2 mitofusin 2 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220811 MGI PMID:35493072 732570 Mfn2 mitofusin 2 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20220811 MGI PMID:35493072 732570 Mfn2 mitofusin 2 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20220811 MGI PMID:35493072 732570 Mfn2 mitofusin 2 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:22619176 732570 Mfn2 mitofusin 2 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20335458 732570 Mfn2 mitofusin 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732570 Mfn2 mitofusin 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12527753 732570 Mfn2 mitofusin 2 gene MP:0011392 increased fetal cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22619176 732570 Mfn2 mitofusin 2 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20141003 MGI PMID:22914740 732570 Mfn2 mitofusin 2 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0014330 abnormal Purkinje cell focal axonal swelling IAGP N RGD:5509061 20240718 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0014331 abnormal Purkinje cell mitochondrial morphology IAGP N RGD:5509061 20240718 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0014345 abnormal neuron mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:17693261 732570 Mfn2 mitofusin 2 gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20230413 MGI PMID:33674260 732570 Mfn2 mitofusin 2 gene MP:0030937 increased mitochondrial DNA content IAGP N RGD:5509061 20230413 MGI PMID:33674260 732571 Fhit fragile histidine triad gene gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:11517343 732571 Fhit fragile histidine triad gene gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16672365 732571 Fhit fragile histidine triad gene gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:15467769 732571 Fhit fragile histidine triad gene gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:15467769 732571 Fhit fragile histidine triad gene gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11517343 732571 Fhit fragile histidine triad gene gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12748294 732571 Fhit fragile histidine triad gene gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15467769 732571 Fhit fragile histidine triad gene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11517343 732571 Fhit fragile histidine triad gene gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:11517343 732571 Fhit fragile histidine triad gene gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15467769 732571 Fhit fragile histidine triad gene gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:10758156 732571 Fhit fragile histidine triad gene gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11517343 732571 Fhit fragile histidine triad gene gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16672365 732571 Fhit fragile histidine triad gene gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15467769 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20201210 MGI PMID:32709928 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0004043 abnormal pH regulation IAGP N RGD:5509061 20201210 MGI PMID:32709928 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20201210 MGI PMID:32709928 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20201210 MGI PMID:32709928 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20201210 MGI PMID:32709928 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20201210 MGI PMID:32709928 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20201210 MGI PMID:32709928 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20201210 MGI PMID:32709928 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20201210 MGI PMID:32709928 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20201210 MGI PMID:32709928 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20201210 MGI PMID:32709928 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0008091 decreased T-helper 2 cell number IAGP N RGD:5509061 20201210 MGI PMID:32709928 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20201210 MGI PMID:32709928 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20201210 MGI PMID:32709928 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20210826 MGI PMID:33914812 732574 Pgam1 phosphoglycerate mutase 1 gene MP:0013762 abnormal effector T cell number IAGP N RGD:5509061 20201210 MGI PMID:32709928 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:12387789 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11980879 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0001889 delayed brain development IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11980879 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:11980879 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20181227 MGI 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11980879 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20230601 MGI 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:12387789 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:12387789 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:11980879 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0008520 disorganized retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:11980879 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11980879 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0012718 decreased hemangioblast number IAGP N RGD:5509061 20141003 MGI PMID:16946137 732577 Cacnb2 calcium channel, voltage-dependent, beta 2 subunit gene MP:0030313 abnormal face development IAGP N RGD:5509061 20171109 MGI PMID:16946137 732579 Lgals8 lectin, galactose binding, soluble 8 gene MP:0001399 hyperactivity IEA N RGD:5509061 20111116 MGI 732579 Lgals8 lectin, galactose binding, soluble 8 gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20170309 MGI PMID:27066737 732579 Lgals8 lectin, galactose binding, soluble 8 gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:27066737 732581 Maob monoamine oxidase B gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:15272015 732581 Maob monoamine oxidase B gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15272015 732581 Maob monoamine oxidase B gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:15272015 732581 Maob monoamine oxidase B gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:15272015 732581 Maob monoamine oxidase B gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9326944 732581 Maob monoamine oxidase B gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:15272015 732581 Maob monoamine oxidase B gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:9326944 732581 Maob monoamine oxidase B gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20180920 MGI PMID:15272015 732581 Maob monoamine oxidase B gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:9326944 732583 Msra methionine sulfoxide reductase A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22521563 732583 Msra methionine sulfoxide reductase A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11606777 732583 Msra methionine sulfoxide reductase A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22521563 732583 Msra methionine sulfoxide reductase A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11606777 732583 Msra methionine sulfoxide reductase A gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:11606777 732583 Msra methionine sulfoxide reductase A gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:11606777 732587 Cacng7 calcium channel, voltage-dependent, gamma subunit 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20529126 732587 Cacng7 calcium channel, voltage-dependent, gamma subunit 7 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20529126 732587 Cacng7 calcium channel, voltage-dependent, gamma subunit 7 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20529126 732587 Cacng7 calcium channel, voltage-dependent, gamma subunit 7 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20529126 732587 Cacng7 calcium channel, voltage-dependent, gamma subunit 7 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:20529126 732587 Cacng7 calcium channel, voltage-dependent, gamma subunit 7 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 732587 Cacng7 calcium channel, voltage-dependent, gamma subunit 7 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20529126 732587 Cacng7 calcium channel, voltage-dependent, gamma subunit 7 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:20529126 732587 Cacng7 calcium channel, voltage-dependent, gamma subunit 7 gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20240523 MGI 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17124501 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17124501 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:17124501 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17124501 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20674857 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:17124501 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17124501 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17124501 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21241895 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:20674857 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20674857 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20141003 MGI PMID:17124501 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20674857 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20674857 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:20674857 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:21241895 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21241895 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:17124501 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:17124501 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:20674857 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:17124501 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20674857 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20674857 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20674857 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20674857 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0005661 decreased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:20674857 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:20674857 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0010104 enlarged thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:17124501 732588 Rims2 regulating synaptic membrane exocytosis 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17124501 732593 Mmp24 matrix metallopeptidase 24 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:14741353 732593 Mmp24 matrix metallopeptidase 24 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:14741353 732593 Mmp24 matrix metallopeptidase 24 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:14741353 732593 Mmp24 matrix metallopeptidase 24 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:14741353 732593 Mmp24 matrix metallopeptidase 24 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:14741353 732593 Mmp24 matrix metallopeptidase 24 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:19805319 732593 Mmp24 matrix metallopeptidase 24 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:19805319 732593 Mmp24 matrix metallopeptidase 24 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:14741353 732593 Mmp24 matrix metallopeptidase 24 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:19805319 732593 Mmp24 matrix metallopeptidase 24 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19805319 732593 Mmp24 matrix metallopeptidase 24 gene MP:0008763 abnormal mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:19805319 732593 Mmp24 matrix metallopeptidase 24 gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:19805319 732594 Vav1 vav 1 oncogene gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19139088 732594 Vav1 vav 1 oncogene gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:19139088 732594 Vav1 vav 1 oncogene gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19009524 732594 Vav1 vav 1 oncogene gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20009105 732594 Vav1 vav 1 oncogene gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:20009105 732594 Vav1 vav 1 oncogene gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:19139088 732594 Vav1 vav 1 oncogene gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:10384109 732594 Vav1 vav 1 oncogene gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9354466 732594 Vav1 vav 1 oncogene gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9601639 732594 Vav1 vav 1 oncogene gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16169499 732594 Vav1 vav 1 oncogene gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:9601639 732594 Vav1 vav 1 oncogene gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9601639 732594 Vav1 vav 1 oncogene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16169499 732594 Vav1 vav 1 oncogene gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9354466 732594 Vav1 vav 1 oncogene gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16169499 732594 Vav1 vav 1 oncogene gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9354466 732594 Vav1 vav 1 oncogene gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11070165 732594 Vav1 vav 1 oncogene gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16169499 732594 Vav1 vav 1 oncogene gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17923690 732594 Vav1 vav 1 oncogene gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19009524 732594 Vav1 vav 1 oncogene gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20009105 732594 Vav1 vav 1 oncogene gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9354466 732594 Vav1 vav 1 oncogene gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17158234 732594 Vav1 vav 1 oncogene gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:10384109 732594 Vav1 vav 1 oncogene gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17158234 732594 Vav1 vav 1 oncogene gene MP:0002491 decreased IgD level IEA N RGD:5509061 20181011 MGI 732594 Vav1 vav 1 oncogene gene MP:0002494 increased IgM level IEA N RGD:5509061 20181011 MGI 732594 Vav1 vav 1 oncogene gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:20009105 732594 Vav1 vav 1 oncogene gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:7828581 732594 Vav1 vav 1 oncogene gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:7828581 732594 Vav1 vav 1 oncogene gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20009105 732594 Vav1 vav 1 oncogene gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:16169499 732594 Vav1 vav 1 oncogene gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:9354466 732594 Vav1 vav 1 oncogene gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:19009524 732594 Vav1 vav 1 oncogene gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:10384109 732594 Vav1 vav 1 oncogene gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:9601639 732594 Vav1 vav 1 oncogene gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19009524 732594 Vav1 vav 1 oncogene gene MP:0005015 increased T cell number IEA N RGD:5509061 20141003 MGI 732594 Vav1 vav 1 oncogene gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11376342 732594 Vav1 vav 1 oncogene gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19009524 732594 Vav1 vav 1 oncogene gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:10384109 732594 Vav1 vav 1 oncogene gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11500824 732594 Vav1 vav 1 oncogene gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16169499 732594 Vav1 vav 1 oncogene gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:20009105 732594 Vav1 vav 1 oncogene gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:9601639 732594 Vav1 vav 1 oncogene gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19009524 732594 Vav1 vav 1 oncogene gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20009105 732594 Vav1 vav 1 oncogene gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9354466 732594 Vav1 vav 1 oncogene gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10384109 732594 Vav1 vav 1 oncogene gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11376342 732594 Vav1 vav 1 oncogene gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16169499 732594 Vav1 vav 1 oncogene gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17923690 732594 Vav1 vav 1 oncogene gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9601639 732594 Vav1 vav 1 oncogene gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20009105 732594 Vav1 vav 1 oncogene gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:20009105 732594 Vav1 vav 1 oncogene gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:9601639 732594 Vav1 vav 1 oncogene gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19009524 732594 Vav1 vav 1 oncogene gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19009524 732594 Vav1 vav 1 oncogene gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:11500824 732594 Vav1 vav 1 oncogene gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11376342 732594 Vav1 vav 1 oncogene gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16169499 732594 Vav1 vav 1 oncogene gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19009524 732594 Vav1 vav 1 oncogene gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9601639 732594 Vav1 vav 1 oncogene gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19009524 732594 Vav1 vav 1 oncogene gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11376342 732594 Vav1 vav 1 oncogene gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19009524 732594 Vav1 vav 1 oncogene gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9601639 732594 Vav1 vav 1 oncogene gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19009524 732594 Vav1 vav 1 oncogene gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9354466 732594 Vav1 vav 1 oncogene gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:11376342 732594 Vav1 vav 1 oncogene gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11376342 732594 Vav1 vav 1 oncogene gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11376342 732594 Vav1 vav 1 oncogene gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:10384109 732594 Vav1 vav 1 oncogene gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:10384109 732594 Vav1 vav 1 oncogene gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17158234 732594 Vav1 vav 1 oncogene gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17923690 732594 Vav1 vav 1 oncogene gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:20009105 732594 Vav1 vav 1 oncogene gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:17158234 732594 Vav1 vav 1 oncogene gene MP:0008686 abnormal interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:20009105 732594 Vav1 vav 1 oncogene gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17923690 732594 Vav1 vav 1 oncogene gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:9601639 732594 Vav1 vav 1 oncogene gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:11500824 732594 Vav1 vav 1 oncogene gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:11376343 732594 Vav1 vav 1 oncogene gene MP:0009922 increased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0010131 increased DN2 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20009105 732594 Vav1 vav 1 oncogene gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:20009105 732594 Vav1 vav 1 oncogene gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22683124 732594 Vav1 vav 1 oncogene gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 732594 Vav1 vav 1 oncogene gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 732594 Vav1 vav 1 oncogene gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 732594 Vav1 vav 1 oncogene gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190411 MGI 732594 Vav1 vav 1 oncogene gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7828581 732594 Vav1 vav 1 oncogene gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 732594 Vav1 vav 1 oncogene gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:11376342 732594 Vav1 vav 1 oncogene gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:14623913 732594 Vav1 vav 1 oncogene gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20190411 MGI 732598 Acmsd amino carboxymuconate semialdehyde decarboxylase gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20181227 MGI 732598 Acmsd amino carboxymuconate semialdehyde decarboxylase gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 732598 Acmsd amino carboxymuconate semialdehyde decarboxylase gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20210128 MGI 732600 Chrna1 cholinergic receptor nicotinic alpha 1 subunit gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:20498043 732600 Chrna1 cholinergic receptor nicotinic alpha 1 subunit gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:20498043 732600 Chrna1 cholinergic receptor nicotinic alpha 1 subunit gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20498043 732600 Chrna1 cholinergic receptor nicotinic alpha 1 subunit gene MP:0001054 failure of neuromuscular synapse presynaptic differentiation IAGP N RGD:5509061 20141003 MGI PMID:20498043 732600 Chrna1 cholinergic receptor nicotinic alpha 1 subunit gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20498043 732600 Chrna1 cholinergic receptor nicotinic alpha 1 subunit gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20141003 MGI PMID:20498043 732600 Chrna1 cholinergic receptor nicotinic alpha 1 subunit gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:20498043 732600 Chrna1 cholinergic receptor nicotinic alpha 1 subunit gene MP:0005162 carpoptosis IAGP N RGD:5509061 20141003 MGI PMID:20498043 732600 Chrna1 cholinergic receptor nicotinic alpha 1 subunit gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:20498043 732600 Chrna1 cholinergic receptor nicotinic alpha 1 subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732604 Itpka inositol 1,4,5-trisphosphate 3-kinase A gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10454357 732607 Stmn2 stathmin-like 2 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 732607 Stmn2 stathmin-like 2 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20230601 MGI 732607 Stmn2 stathmin-like 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20230601 MGI 732607 Stmn2 stathmin-like 2 gene MP:0001924 infertility IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0002946 delayed axon extension IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230601 MGI 732607 Stmn2 stathmin-like 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20230601 MGI 732607 Stmn2 stathmin-like 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0020850 abnormal microtubule cytoskeleton morphology IAGP N RGD:5509061 20230914 MGI PMID:35767949 732607 Stmn2 stathmin-like 2 gene MP:0020955 increased mechanical nociceptive threshold IAGP N RGD:5509061 20230914 MGI PMID:35767949 732608 Epcam epithelial cell adhesion molecule gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:23209569 732608 Epcam epithelial cell adhesion molecule gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:24337010 732608 Epcam epithelial cell adhesion molecule gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23209569 732608 Epcam epithelial cell adhesion molecule gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23209569 732608 Epcam epithelial cell adhesion molecule gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:23209569 732608 Epcam epithelial cell adhesion molecule gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:23209569 732608 Epcam epithelial cell adhesion molecule gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:22819673 732608 Epcam epithelial cell adhesion molecule gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:23209569 732608 Epcam epithelial cell adhesion molecule gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24337010 732608 Epcam epithelial cell adhesion molecule gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23209569 732608 Epcam epithelial cell adhesion molecule gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20046825 732608 Epcam epithelial cell adhesion molecule gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:20046825 732608 Epcam epithelial cell adhesion molecule gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:20046825 732608 Epcam epithelial cell adhesion molecule gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:20046825 732608 Epcam epithelial cell adhesion molecule gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22819673 732608 Epcam epithelial cell adhesion molecule gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23209569 732608 Epcam epithelial cell adhesion molecule gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24337010 732608 Epcam epithelial cell adhesion molecule gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:24337010 732608 Epcam epithelial cell adhesion molecule gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:20046825 732608 Epcam epithelial cell adhesion molecule gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:22411813 732608 Epcam epithelial cell adhesion molecule gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:24337010 732608 Epcam epithelial cell adhesion molecule gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:24337010 732608 Epcam epithelial cell adhesion molecule gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:24337010 732608 Epcam epithelial cell adhesion molecule gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:20046825 732608 Epcam epithelial cell adhesion molecule gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20141003 MGI PMID:24337010 732608 Epcam epithelial cell adhesion molecule gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:20046825 732608 Epcam epithelial cell adhesion molecule gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:22819673 732608 Epcam epithelial cell adhesion molecule gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:20046825 732608 Epcam epithelial cell adhesion molecule gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:24337010 732608 Epcam epithelial cell adhesion molecule gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22411813 732608 Epcam epithelial cell adhesion molecule gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:22411813 732608 Epcam epithelial cell adhesion molecule gene MP:0008117 abnormal Langerhans cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22411813 732608 Epcam epithelial cell adhesion molecule gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:23209569 732608 Epcam epithelial cell adhesion molecule gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:24337010 732608 Epcam epithelial cell adhesion molecule gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:24337010 732608 Epcam epithelial cell adhesion molecule gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:22819673 732608 Epcam epithelial cell adhesion molecule gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:23209569 732608 Epcam epithelial cell adhesion molecule gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:24337010 732608 Epcam epithelial cell adhesion molecule gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23209569 732608 Epcam epithelial cell adhesion molecule gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24337010 732608 Epcam epithelial cell adhesion molecule gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20046825 732608 Epcam epithelial cell adhesion molecule gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22819673 732608 Epcam epithelial cell adhesion molecule gene MP:0014083 blunted small intestinal villi IAGP N RGD:5509061 20160310 MGI PMID:24337010 732608 Epcam epithelial cell adhesion molecule gene MP:0031154 intestinal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:22819673 732610 Tekt1 tektin 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 732610 Tekt1 tektin 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 732610 Tekt1 tektin 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 732610 Tekt1 tektin 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 732610 Tekt1 tektin 1 gene MP:0002217 small lymph nodes IEA N RGD:5509061 20230601 MGI 732610 Tekt1 tektin 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 732610 Tekt1 tektin 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:20975042 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:20975042 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12397017 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20975042 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20740013 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20975042 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:20975042 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:20975042 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:20975042 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:20740013 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0008556 abnormal tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20975042 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20740013 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20740013 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:20740013 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0008656 abnormal interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20975042 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0008704 abnormal interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20975042 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:20740013 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20740013 732612 Nfkbib nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, beta gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20975042 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:20128845 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20128845 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20128845 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:20128845 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0003280 urinary incontinence IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0003619 abnormal urine color IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20150910 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:20128845 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0006276 abnormal autonomic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0009511 distended stomach IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0009646 urinary bladder inflammation IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:10771006 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20128845 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0011625 cystolithiasis IAGP N RGD:5509061 20141003 MGI PMID:10318955 732614 Chrna3 cholinergic receptor, nicotinic, alpha polypeptide 3 gene MP:0011766 abnormal urinary bladder mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10318955 732618 Car2 carbonic anhydrase 2 gene MP:0000525 renal tubular acidosis IAGP N RGD:5509061 20141003 MGI PMID:3126501 732618 Car2 carbonic anhydrase 2 gene MP:0000525 renal tubular acidosis IAGP N RGD:5509061 20150827 MGI PMID:25143453 732618 Car2 carbonic anhydrase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150827 MGI PMID:25143453 732618 Car2 carbonic anhydrase 2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:16217040 732618 Car2 carbonic anhydrase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:3126501 732618 Car2 carbonic anhydrase 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11698654 732618 Car2 carbonic anhydrase 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20150827 MGI PMID:25143453 732618 Car2 carbonic anhydrase 2 gene MP:0003017 decreased circulating bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:3126501 732618 Car2 carbonic anhydrase 2 gene MP:0003017 decreased circulating bicarbonate level IAGP N RGD:5509061 20150827 MGI PMID:25143453 732618 Car2 carbonic anhydrase 2 gene MP:0003027 abnormal blood pH regulation IAGP N RGD:5509061 20150827 MGI PMID:25143453 732618 Car2 carbonic anhydrase 2 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:16217040 732618 Car2 carbonic anhydrase 2 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:23881097 732618 Car2 carbonic anhydrase 2 gene MP:0004119 hypokalemia IAGP N RGD:5509061 20150827 MGI PMID:25143453 732618 Car2 carbonic anhydrase 2 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:16217040 732618 Car2 carbonic anhydrase 2 gene MP:0005493 stomach epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16217040 732618 Car2 carbonic anhydrase 2 gene MP:0006423 dilated rete testis IAGP N RGD:5509061 20141003 MGI PMID:11698654 732618 Car2 carbonic anhydrase 2 gene MP:0009140 dilated efferent ductule of testis IAGP N RGD:5509061 20141003 MGI PMID:11698654 732618 Car2 carbonic anhydrase 2 gene MP:0009349 increased urine pH IAGP N RGD:5509061 20150827 MGI PMID:25143453 732618 Car2 carbonic anhydrase 2 gene MP:0010787 gastric cyst IAGP N RGD:5509061 20141003 MGI PMID:16217040 732618 Car2 carbonic anhydrase 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16217040 732618 Car2 carbonic anhydrase 2 gene MP:0011403 pyelonephritis IAGP N RGD:5509061 20150827 MGI PMID:25143453 732618 Car2 carbonic anhydrase 2 gene MP:0011754 abnormal kidney collecting duct intercalated cell morphology IAGP N RGD:5509061 20150827 MGI PMID:25143453 732618 Car2 carbonic anhydrase 2 gene MP:0012550 respiratory acidosis IAGP N RGD:5509061 20170921 MGI PMID:16217040 732618 Car2 carbonic anhydrase 2 gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20150827 MGI PMID:25143453 732618 Car2 carbonic anhydrase 2 gene MP:0013567 gastric gland atrophy IAGP N RGD:5509061 20150312 MGI PMID:16217040 732620 Clcn4 chloride channel, voltage-sensitive 4 gene MP:0011445 abnormal renal protein reabsorption IAGP N RGD:5509061 20141003 MGI PMID:20351103 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:23922682 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0000461 decreased presacral vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:23922682 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0001284 absent vibrissae IEA N RGD:5509061 20200514 MGI 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23922682 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:23922682 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20221215 MGI 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0002764 short tibia IEA N RGD:5509061 20201022 MGI 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:23922682 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:23922682 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:23922682 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:23922682 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:23922682 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0004622 sacral vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:23922682 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20220811 MGI 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0008528 polycystic kidney IEA N RGD:5509061 20200514 MGI 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17945361 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0009709 hydrometra IEA N RGD:5509061 20200514 MGI 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:17945361 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:17945361 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23922682 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20240523 MGI 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23922682 732622 Nacc1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20200514 MGI 732623 Plaa phospholipase A2, activating protein gene MP:0000160 kyphosis IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0000745 tremors IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0000746 weakness IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0000753 paralysis IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0000774 decreased brain size IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0000852 small cerebellum IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0001393 ataxia IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0001406 abnormal gait IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0001513 limb grasping IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0001525 impaired balance IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0001954 respiratory distress IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0002183 gliosis IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0009434 paraparesis IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0010008 abnormal Purkinje cell migration IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20180503 MGI PMID:28413018 732623 Plaa phospholipase A2, activating protein gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:28413018 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:22327219 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21300983 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21300983 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22327219 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22327219 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22327219 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:22327219 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21300983 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15798218 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22327219 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:22327219 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23799077 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:22327219 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21300983 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21300983 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21300983 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:21300983 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23799077 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21300983 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 732625 Birc2 baculoviral IAP repeat-containing 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 732627 Ralbp1 ralA binding protein 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20141003 MGI 732627 Ralbp1 ralA binding protein 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20141003 MGI 732627 Ralbp1 ralA binding protein 1 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:19823667 732627 Ralbp1 ralA binding protein 1 gene MP:0003043 hypoalgesia IEA N RGD:5509061 20141003 MGI 732627 Ralbp1 ralA binding protein 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:16024601 732627 Ralbp1 ralA binding protein 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16024601 732628 Nap1l1 nucleosome assembly protein 1-like 1 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20180920 MGI PMID:29490266 732628 Nap1l1 nucleosome assembly protein 1-like 1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20180920 MGI PMID:29490266 732628 Nap1l1 nucleosome assembly protein 1-like 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20180920 MGI PMID:29490266 732628 Nap1l1 nucleosome assembly protein 1-like 1 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20180920 MGI PMID:29490266 732629 Cdk11b cyclin dependent kinase 11B gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15060143 732629 Cdk11b cyclin dependent kinase 11B gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:17389615 732629 Cdk11b cyclin dependent kinase 11B gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15060143 732629 Cdk11b cyclin dependent kinase 11B gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:17389615 732629 Cdk11b cyclin dependent kinase 11B gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:17389615 732629 Cdk11b cyclin dependent kinase 11B gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:15060143 732629 Cdk11b cyclin dependent kinase 11B gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15060143 732629 Cdk11b cyclin dependent kinase 11B gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:15060143 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20181227 MGI 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0000691 enlarged spleen IEA N RGD:5509061 20181227 MGI 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20181227 MGI 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0000706 small thymus IEA N RGD:5509061 20181227 MGI 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21460847 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20170105 MGI 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210128 MGI 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:20080759 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21460847 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:20080759 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:21460847 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:19749763 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:19995955 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0005542 cornea vascularization IEA N RGD:5509061 20240523 MGI 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:19749763 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19749763 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19995955 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19749763 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19749763 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19995955 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20230413 MGI PMID:35732734 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20080759 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:21460847 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19749763 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19995955 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:22346732 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21460847 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:22346732 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:21460847 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:22346732 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:22346732 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20080759 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0008712 decreased interleukin-9 secretion IAGP N RGD:5509061 20141003 MGI PMID:22346732 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0010219 increased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0011078 increased macrophage cytokine production IAGP N RGD:5509061 20141003 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0013795 abnormal colon goblet cell morphology IAGP N RGD:5509061 20150618 MGI PMID:24442434 732632 Nfil3 nuclear factor, interleukin 3, regulated gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:24442434 732633 Ebf1 early B cell factor 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19130908 732633 Ebf1 early B cell factor 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 732633 Ebf1 early B cell factor 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 732633 Ebf1 early B cell factor 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19130908 732633 Ebf1 early B cell factor 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 732633 Ebf1 early B cell factor 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 732633 Ebf1 early B cell factor 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 732633 Ebf1 early B cell factor 1 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 732633 Ebf1 early B cell factor 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 732633 Ebf1 early B cell factor 1 gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:11076752 732633 Ebf1 early B cell factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19130908 732633 Ebf1 early B cell factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7542362 732633 Ebf1 early B cell factor 1 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 732633 Ebf1 early B cell factor 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230601 MGI 732633 Ebf1 early B cell factor 1 gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20181011 MGI 732633 Ebf1 early B cell factor 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22431510 732633 Ebf1 early B cell factor 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7542362 732633 Ebf1 early B cell factor 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:7542362 732633 Ebf1 early B cell factor 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 732633 Ebf1 early B cell factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19130908 732633 Ebf1 early B cell factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7542362 732633 Ebf1 early B cell factor 1 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 732633 Ebf1 early B cell factor 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 732633 Ebf1 early B cell factor 1 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:19130908 732633 Ebf1 early B cell factor 1 gene MP:0002491 decreased IgD level IEA N RGD:5509061 20181011 MGI 732633 Ebf1 early B cell factor 1 gene MP:0002494 increased IgM level IEA N RGD:5509061 20181011 MGI 732633 Ebf1 early B cell factor 1 gene MP:0002619 abnormal lymphocyte morphology IEA N RGD:5509061 20190418 MGI 732633 Ebf1 early B cell factor 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19130908 732633 Ebf1 early B cell factor 1 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20221215 MGI 732633 Ebf1 early B cell factor 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19130908 732633 Ebf1 early B cell factor 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:19130908 732633 Ebf1 early B cell factor 1 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:10556054 732633 Ebf1 early B cell factor 1 gene MP:0004103 abnormal ventral striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:10556054 732633 Ebf1 early B cell factor 1 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:10556054 732633 Ebf1 early B cell factor 1 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7542362 732633 Ebf1 early B cell factor 1 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22431510 732633 Ebf1 early B cell factor 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:19130908 732633 Ebf1 early B cell factor 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:19130908 732633 Ebf1 early B cell factor 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22431510 732633 Ebf1 early B cell factor 1 gene MP:0005015 increased T cell number IEA N RGD:5509061 20181011 MGI 732633 Ebf1 early B cell factor 1 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20111116 MGI 732633 Ebf1 early B cell factor 1 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22431510 732633 Ebf1 early B cell factor 1 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20190103 MGI 732633 Ebf1 early B cell factor 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 732633 Ebf1 early B cell factor 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 732633 Ebf1 early B cell factor 1 gene MP:0008082 increased single-positive T cell number IEA N RGD:5509061 20181011 MGI 732633 Ebf1 early B cell factor 1 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:10556054 732633 Ebf1 early B cell factor 1 gene MP:0008167 increased B-1a cell number IEA N RGD:5509061 20181011 MGI 732633 Ebf1 early B cell factor 1 gene MP:0008169 increased B-1b cell number IEA N RGD:5509061 20181011 MGI 732633 Ebf1 early B cell factor 1 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:22431510 732633 Ebf1 early B cell factor 1 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:22431510 732633 Ebf1 early B cell factor 1 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:22431510 732633 Ebf1 early B cell factor 1 gene MP:0008192 abnormal germinal center B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22431510 732633 Ebf1 early B cell factor 1 gene MP:0008202 absent B-1 B cells IAGP N RGD:5509061 20141003 MGI PMID:7542362 732633 Ebf1 early B cell factor 1 gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20181011 MGI 732633 Ebf1 early B cell factor 1 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:7542362 732633 Ebf1 early B cell factor 1 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22431510 732633 Ebf1 early B cell factor 1 gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:7542362 732633 Ebf1 early B cell factor 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22431510 732633 Ebf1 early B cell factor 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19130908 732633 Ebf1 early B cell factor 1 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:22431510 732633 Ebf1 early B cell factor 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:22431510 732633 Ebf1 early B cell factor 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:22431510 732633 Ebf1 early B cell factor 1 gene MP:0008560 increased tumor necrosis factor secretion IEA N RGD:5509061 20181011 MGI 732633 Ebf1 early B cell factor 1 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22431510 732633 Ebf1 early B cell factor 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19130908 732633 Ebf1 early B cell factor 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200514 MGI 732633 Ebf1 early B cell factor 1 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:19130908 732633 Ebf1 early B cell factor 1 gene MP:0010845 decreased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 732633 Ebf1 early B cell factor 1 gene MP:0010860 abnormal anterior commissure pars posterior morphology IAGP N RGD:5509061 20141003 MGI PMID:10556054 732633 Ebf1 early B cell factor 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 732633 Ebf1 early B cell factor 1 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:10556054 732633 Ebf1 early B cell factor 1 gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 732633 Ebf1 early B cell factor 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:19130908 732633 Ebf1 early B cell factor 1 gene MP:0020138 delayed bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:19130908 732635 Prpf19 pre-mRNA processing factor 19 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17283042 732635 Prpf19 pre-mRNA processing factor 19 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17283042 732635 Prpf19 pre-mRNA processing factor 19 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17283042 732635 Prpf19 pre-mRNA processing factor 19 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17283042 732635 Prpf19 pre-mRNA processing factor 19 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:17283042 732636 Inhbe inhibin beta-E gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10913194 732636 Inhbe inhibin beta-E gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20810712 732637 Ctsd cathepsin D gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11567042 732637 Ctsd cathepsin D gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 732637 Ctsd cathepsin D gene MP:0000427 abnormal hair cycle IEA N RGD:5509061 20160331 MGI 732637 Ctsd cathepsin D gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:7641679 732637 Ctsd cathepsin D gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:11567042 732637 Ctsd cathepsin D gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:7641679 732637 Ctsd cathepsin D gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20160128 MGI PMID:26232697 732637 Ctsd cathepsin D gene MP:0000746 weakness IEA N RGD:5509061 20160331 MGI 732637 Ctsd cathepsin D gene MP:0000811 hippocampal neuron degeneration IEA N RGD:5509061 20160331 MGI 732637 Ctsd cathepsin D gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11567042 732637 Ctsd cathepsin D gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7641679 732637 Ctsd cathepsin D gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160128 MGI PMID:26232697 732637 Ctsd cathepsin D gene MP:0001263 weight loss IAGP N RGD:5509061 20160128 MGI PMID:26232697 732637 Ctsd cathepsin D gene MP:0001314 cornea opacity IEA N RGD:5509061 20240523 MGI 732637 Ctsd cathepsin D gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:12676526 732637 Ctsd cathepsin D gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:7641679 732637 Ctsd cathepsin D gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7641679 732637 Ctsd cathepsin D gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:9539769 732637 Ctsd cathepsin D gene MP:0001967 deafness IEA N RGD:5509061 20160331 MGI 732637 Ctsd cathepsin D gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:12676526 732637 Ctsd cathepsin D gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10995834 732637 Ctsd cathepsin D gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11567042 732637 Ctsd cathepsin D gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11567042 732637 Ctsd cathepsin D gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7641679 732637 Ctsd cathepsin D gene MP:0002083 premature death IAGP N RGD:5509061 20160128 MGI PMID:26232697 732637 Ctsd cathepsin D gene MP:0002183 gliosis IAGP N RGD:5509061 20160128 MGI PMID:26232697 732637 Ctsd cathepsin D gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:7641679 732637 Ctsd cathepsin D gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:7641679 732637 Ctsd cathepsin D gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:10995834 732637 Ctsd cathepsin D gene MP:0002855 abnormal cochlear ganglion morphology IEA N RGD:5509061 20160331 MGI 732637 Ctsd cathepsin D gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20160128 MGI PMID:26232697 732637 Ctsd cathepsin D gene MP:0003225 axonal dystrophy IEA N RGD:5509061 20160331 MGI 732637 Ctsd cathepsin D gene MP:0003354 astrocytosis IAGP N RGD:5509061 20160128 MGI PMID:26232697 732637 Ctsd cathepsin D gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20160128 MGI PMID:26232697 732637 Ctsd cathepsin D gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7641679 732637 Ctsd cathepsin D gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:7641679 732637 Ctsd cathepsin D gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20141003 MGI PMID:10995834 732637 Ctsd cathepsin D gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:7641679 732637 Ctsd cathepsin D gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20160128 MGI PMID:26232697 732637 Ctsd cathepsin D gene MP:0005150 cachexia IEA N RGD:5509061 20160331 MGI 732637 Ctsd cathepsin D gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:7641679 732637 Ctsd cathepsin D gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20210128 MGI 732637 Ctsd cathepsin D gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:12676526 732637 Ctsd cathepsin D gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:7641679 732637 Ctsd cathepsin D gene MP:0008918 microgliosis IAGP N RGD:5509061 20160128 MGI PMID:26232697 732637 Ctsd cathepsin D gene MP:0010783 abnormal stomach wall morphology IEA N RGD:5509061 20160331 MGI 732637 Ctsd cathepsin D gene MP:0011083 lethality at weaning, complete penetrance IEA N RGD:5509061 20160331 MGI 732637 Ctsd cathepsin D gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20160331 MGI 732637 Ctsd cathepsin D gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20160331 MGI 732637 Ctsd cathepsin D gene MP:0011940 decreased food intake IAGP N RGD:5509061 20201224 MGI PMID:7641679 732637 Ctsd cathepsin D gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20160331 MGI 732637 Ctsd cathepsin D gene MP:0012504 increased forebrain apoptosis IAGP N RGD:5509061 20201224 MGI PMID:11567042 732637 Ctsd cathepsin D gene MP:0014078 small intestinal villus atrophy IAGP N RGD:5509061 20160310 MGI PMID:26232697 732637 Ctsd cathepsin D gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20160310 MGI PMID:26232697 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0000184 abnormal circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11495927 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11723064 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:9739042 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10801788 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9739042 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:10377439 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:7539101 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7539101 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10951268 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12485431 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:12485431 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11495927 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20211125 MGI PMID:33279456 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200514 MGI 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:10801788 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11495927 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:10377439 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16054078 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11723064 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:10801788 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:10801788 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10377439 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16054054 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16054078 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:10377439 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:11495927 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:7539101 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:9739042 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:10951268 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16054054 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:11514592 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20190725 MGI PMID:28205547 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10801788 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0003457 abnormal circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:10377439 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:12847522 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:10801788 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:10801788 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11495927 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16054078 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16054054 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16054054 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10377439 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:10801788 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:12552126 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11723064 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16054078 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:16054054 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10801788 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:10801788 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10801788 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20190725 MGI PMID:28205547 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20211125 MGI PMID:33279456 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11495927 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0009598 thin epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:10951268 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0009605 decreased keratohyalin granule number IAGP N RGD:5509061 20141003 MGI PMID:10951268 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10377439 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9739042 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20211125 MGI PMID:33279456 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12847522 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:9739042 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:21641555 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20200514 MGI 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20190725 MGI PMID:28205547 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:21641555 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20211125 MGI PMID:33279456 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:16054054 732638 Ppara peroxisome proliferator activated receptor alpha gene MP:0031415 increased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:16054054 732640 Grpel1 GrpE-like 1, mitochondrial gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20230105 MGI PMID:36198903 732640 Grpel1 GrpE-like 1, mitochondrial gene MP:0001263 weight loss IAGP N RGD:5509061 20230105 MGI PMID:36198903 732640 Grpel1 GrpE-like 1, mitochondrial gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20230105 MGI PMID:36198903 732640 Grpel1 GrpE-like 1, mitochondrial gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20230105 MGI PMID:36198903 732640 Grpel1 GrpE-like 1, mitochondrial gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20230105 MGI PMID:36198903 732640 Grpel1 GrpE-like 1, mitochondrial gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20230105 MGI PMID:36198903 732640 Grpel1 GrpE-like 1, mitochondrial gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20230105 MGI PMID:36198903 732640 Grpel1 GrpE-like 1, mitochondrial gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20230105 MGI PMID:36198903 732640 Grpel1 GrpE-like 1, mitochondrial gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20230105 MGI PMID:36198903 732642 Oga O-GlcNAcase gene MP:0001177 atelectasis IAGP N RGD:5509061 20150917 MGI PMID:22314054 732642 Oga O-GlcNAcase gene MP:0001953 respiratory failure IAGP N RGD:5509061 20150917 MGI PMID:22314054 732642 Oga O-GlcNAcase gene MP:0004024 aneuploidy IAGP N RGD:5509061 20150917 MGI PMID:22314054 732642 Oga O-GlcNAcase gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20150917 MGI PMID:22314054 732642 Oga O-GlcNAcase gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20150917 MGI PMID:22314054 732642 Oga O-GlcNAcase gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20150917 MGI PMID:22314054 732642 Oga O-GlcNAcase gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20150917 MGI PMID:22314054 732642 Oga O-GlcNAcase gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20150917 MGI PMID:22314054 732642 Oga O-GlcNAcase gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20150917 MGI PMID:22314054 732642 Oga O-GlcNAcase gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20150917 MGI PMID:22314054 732642 Oga O-GlcNAcase gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20150917 MGI PMID:22314054 732642 Oga O-GlcNAcase gene MP:0013289 abnormal mitotic cytokinesis IAGP N RGD:5509061 20150917 MGI PMID:22314054 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18460329 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:14586002 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18460329 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:14586002 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0002969 impaired social transmission of food preference IAGP N RGD:5509061 20141003 MGI PMID:14586002 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18460329 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18460329 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19864584 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18460329 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:18460329 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:18460329 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18460329 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19864584 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:18460329 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:18460329 732643 Camkk2 calcium/calmodulin-dependent protein kinase kinase 2, beta gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:18460329 732646 Tkt transketolase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12167708 732646 Tkt transketolase gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:12167708 732646 Tkt transketolase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12167708 732646 Tkt transketolase gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12167708 732646 Tkt transketolase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:12167708 732646 Tkt transketolase gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:12167708 732646 Tkt transketolase gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:12167708 732646 Tkt transketolase gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12167708 732646 Tkt transketolase gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:12167708 732646 Tkt transketolase gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:12167708 732646 Tkt transketolase gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12167708 732646 Tkt transketolase gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20240523 MGI 732646 Tkt transketolase gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12167708 732646 Tkt transketolase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 732646 Tkt transketolase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 732646 Tkt transketolase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210520 MGI 732648 Cnga1 cyclic nucleotide gated channel alpha 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20230302 MGI PMID:36115851 732648 Cnga1 cyclic nucleotide gated channel alpha 1 gene MP:0002001 blindness IAGP N RGD:5509061 20230302 MGI PMID:36115851 732648 Cnga1 cyclic nucleotide gated channel alpha 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20230302 MGI PMID:36115851 732648 Cnga1 cyclic nucleotide gated channel alpha 1 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20230302 MGI PMID:36115851 732648 Cnga1 cyclic nucleotide gated channel alpha 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20230302 MGI PMID:36115851 732648 Cnga1 cyclic nucleotide gated channel alpha 1 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20230302 MGI PMID:36115851 732648 Cnga1 cyclic nucleotide gated channel alpha 1 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20230302 MGI PMID:36115851 732648 Cnga1 cyclic nucleotide gated channel alpha 1 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20230302 MGI PMID:36115851 732648 Cnga1 cyclic nucleotide gated channel alpha 1 gene MP:0008580 photoreceptor inner segment degeneration IAGP N RGD:5509061 20230302 MGI PMID:36115851 732648 Cnga1 cyclic nucleotide gated channel alpha 1 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20230302 MGI PMID:36115851 732648 Cnga1 cyclic nucleotide gated channel alpha 1 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20230302 MGI PMID:36115851 732648 Cnga1 cyclic nucleotide gated channel alpha 1 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20230302 MGI PMID:36115851 732648 Cnga1 cyclic nucleotide gated channel alpha 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20230302 MGI PMID:36115851 732648 Cnga1 cyclic nucleotide gated channel alpha 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20230302 MGI PMID:36115851 732650 Hif3a hypoxia inducible factor 3, alpha subunit gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:18070924 732650 Hif3a hypoxia inducible factor 3, alpha subunit gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:18070924 732650 Hif3a hypoxia inducible factor 3, alpha subunit gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:18070924 732650 Hif3a hypoxia inducible factor 3, alpha subunit gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:18070924 732650 Hif3a hypoxia inducible factor 3, alpha subunit gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18070924 732650 Hif3a hypoxia inducible factor 3, alpha subunit gene MP:0008727 increased heart right atrium size IAGP N RGD:5509061 20141003 MGI PMID:18070924 732650 Hif3a hypoxia inducible factor 3, alpha subunit gene MP:0010563 increased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:18070924 732650 Hif3a hypoxia inducible factor 3, alpha subunit gene MP:0010755 abnormal heart right ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:18070924 732650 Hif3a hypoxia inducible factor 3, alpha subunit gene MP:0010995 abnormal lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:18070924 732650 Hif3a hypoxia inducible factor 3, alpha subunit gene MP:0011144 thin lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:18070924 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18056838 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20141003 MGI PMID:18056838 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:18056838 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:18056838 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18056838 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0001013 enlarged superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:18056838 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0001317 abnormal pupil morphology IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18056838 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23264599 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20733101 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18056838 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22955912 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18056838 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22464323 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:20733101 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:18056838 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:23264599 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0003437 abnormal carotid body morphology IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20733101 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20211021 MGI 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:20733101 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:20733101 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:18056838 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20733101 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20733101 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0005661 decreased circulating adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0005664 decreased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20240523 MGI 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0008289 abnormal adrenal medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0008504 abnormal adrenal chromaffin cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18056838 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18332118 732653 Egln3 egl-9 family hypoxia-inducible factor 3 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20141003 MGI PMID:20733101 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20160421 MGI 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220519 MGI 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22099461 732654 Sh3gl2 SH3-domain GRB2-like 2 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:22099461 732655 Ghrl ghrelin gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17130496 732655 Ghrl ghrelin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17130496 732655 Ghrl ghrelin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14585959 732655 Ghrl ghrelin gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17130496 732655 Ghrl ghrelin gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:16203827 732655 Ghrl ghrelin gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17130496 732655 Ghrl ghrelin gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:16203827 732655 Ghrl ghrelin gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15148384 732655 Ghrl ghrelin gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20171228 MGI PMID:19666521 732655 Ghrl ghrelin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17130496 732655 Ghrl ghrelin gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:15148384 732655 Ghrl ghrelin gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:16203827 732655 Ghrl ghrelin gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20171228 MGI PMID:19666521 732655 Ghrl ghrelin gene MP:0011396 abnormal sleep behavior IAGP N RGD:5509061 20171228 MGI PMID:19666521 732655 Ghrl ghrelin gene MP:0012289 abnormal non-rapid eye movement sleep pattern IAGP N RGD:5509061 20171228 MGI PMID:19666521 732657 Slc8a3 solute carrier family 8 (sodium/calcium exchanger), member 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:14722618 732657 Slc8a3 solute carrier family 8 (sodium/calcium exchanger), member 3 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20160421 MGI 732657 Slc8a3 solute carrier family 8 (sodium/calcium exchanger), member 3 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:18234895 732657 Slc8a3 solute carrier family 8 (sodium/calcium exchanger), member 3 gene MP:0002899 fatigue IAGP N RGD:5509061 20141003 MGI PMID:14722618 732657 Slc8a3 solute carrier family 8 (sodium/calcium exchanger), member 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 732657 Slc8a3 solute carrier family 8 (sodium/calcium exchanger), member 3 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:14722618 732657 Slc8a3 solute carrier family 8 (sodium/calcium exchanger), member 3 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:14722618 732657 Slc8a3 solute carrier family 8 (sodium/calcium exchanger), member 3 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20240523 MGI 732657 Slc8a3 solute carrier family 8 (sodium/calcium exchanger), member 3 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:18234895 732657 Slc8a3 solute carrier family 8 (sodium/calcium exchanger), member 3 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:14722618 732657 Slc8a3 solute carrier family 8 (sodium/calcium exchanger), member 3 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20210520 MGI 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000275 heart hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:9389646 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:12507915 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:12507915 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0000676 abnormal body water content IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:12507915 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23468951 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:23468951 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001435 absent suckling reflex IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001699 increased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12507915 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001699 increased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:23468951 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:11311167 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12507915 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:23468951 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0003121 genetic imprinting IAGP N RGD:5509061 20141003 MGI PMID:12507915 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0003126 abnormal external female genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0003416 premature bone ossification IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0004199 increased fetal size IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0004202 pulmonary hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0004260 enlarged placenta IAGP N RGD:5509061 20141003 MGI PMID:12507915 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0004260 enlarged placenta IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0004882 enlarged lung IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0004906 enlarged uterus IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:23468951 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0004920 increased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:23468951 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0008258 thin endometrium IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:11311167 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20141003 MGI PMID:23468951 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0009085 abnormal uterine horn morphology IAGP N RGD:5509061 20141003 MGI PMID:23468951 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0009087 dilated uterine horn IAGP N RGD:5509061 20141003 MGI PMID:23468951 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0009097 absent endometrial glands IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:11311167 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0009432 increased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:23468951 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0009432 increased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:9389646 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0009673 increased birth weight IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23468951 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0009702 increased birth body size IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0009702 increased birth body size IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0010563 increased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011030 impaired branching involved in preterminal bronchiole morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12507915 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8806824 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9389646 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8001817 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7984240 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12507915 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11311167 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23468951 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0011873 enlarged uterine horn IAGP N RGD:5509061 20141003 MGI PMID:23468951 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:8806828 732661 Igf2r insulin-like growth factor 2 receptor gene MP:0031552 abnormal tricuspid valve development IAGP N RGD:5509061 20240104 MGI PMID:8001817 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10952312 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11395002 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11988168 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:14766174 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16772167 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:10952312 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:11395002 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:14766174 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:11395002 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0001108 absent Schwann cells IAGP N RGD:5509061 20141003 MGI PMID:11395002 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:14766174 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10952312 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10929715 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18434421 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:14766174 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:14766174 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:14766174 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:11395002 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:10952312 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:16772167 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10952312 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14766174 732663 Isl2 insulin related protein 2 (islet 2) gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11395002 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:16219676 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:20103739 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:16219676 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:16219676 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:18347057 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:18347057 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15116068 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:15116068 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19843540 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18347057 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001200 thick skin IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001214 skin hyperplasia IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18396135 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20103739 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16642023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18347057 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16219676 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:18396135 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16642023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:15116068 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:15116068 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15116068 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16219676 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:15116068 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20930845 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:23453624 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16581004 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18396135 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16581004 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16642023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18347057 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16642023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:15116068 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15116068 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20944007 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:18396135 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:20103739 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:16642023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002706 abnormal kidney size IAGP N RGD:5509061 20141003 MGI PMID:18347057 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16642023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:18396135 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20103739 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:18396135 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:16642023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:20930845 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15116068 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:18347057 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0004559 small allantois IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:20103739 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0004972 abnormal regulatory T cell number IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20944007 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20944007 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20944007 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005114 premature hair loss IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16642023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18396135 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16581004 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18347057 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:18347057 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18347057 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16581004 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16642023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18396135 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16642023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18396135 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0005667 abnormal circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18396135 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15116068 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0008036 abnormal NK T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20944007 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:20944007 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0008041 absent NK T cells IAGP N RGD:5509061 20141003 MGI PMID:20944007 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0008130 abnormal pituitary intermediate lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:20103739 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0008324 abnormal melanotroph morphology IAGP N RGD:5509061 20141003 MGI PMID:18396135 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0008341 decreased corticotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:18396135 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0008460 absent dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0008460 absent dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:15116068 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23453624 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0009169 pancreatic islet hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18347057 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:16642023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18396135 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20103739 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0010500 myocardium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12970179 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16219676 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15116068 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20944007 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15116068 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0011156 abnormal hypodermis fat layer morphology IAGP N RGD:5509061 20151217 MGI PMID:26099023 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:20103739 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0012081 absent heart tube IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:15116068 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0012176 abnormal head development IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0012182 abnormal presomitic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0012745 abnormal neural crest cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12110585 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0013344 increased pituitary gland apoptosis IAGP N RGD:5509061 20141204 MGI PMID:20103739 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0013346 increased melanotroph apoptosis IAGP N RGD:5509061 20141204 MGI PMID:20103739 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0013347 increased corticotroph apoptosis IAGP N RGD:5509061 20141204 MGI PMID:20103739 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0014287 decreased adrenal gland zona fasciculata size IAGP N RGD:5509061 20230907 MGI PMID:18347057 732665 Pdpk1 3-phosphoinositide dependent protein kinase 1 gene MP:0014441 decreased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:20103739 732667 Zg16 zymogen granule protein 16 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20170629 MGI PMID:27849619 732667 Zg16 zymogen granule protein 16 gene MP:0001260 increased body weight IAGP N RGD:5509061 20170629 MGI PMID:27849619 732667 Zg16 zymogen granule protein 16 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20170629 MGI PMID:27849619 732667 Zg16 zymogen granule protein 16 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20170629 MGI PMID:27849619 732667 Zg16 zymogen granule protein 16 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20170629 MGI PMID:27849619 732667 Zg16 zymogen granule protein 16 gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20170629 MGI PMID:27849619 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20240523 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11672542 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11672542 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20181227 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11672542 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15219462 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9252121 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15219462 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9252121 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0000706 small thymus IEA N RGD:5509061 20201022 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001606 impaired hematopoiesis IEA N RGD:5509061 20161201 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12563261 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001805 decreased IgG level IEA N RGD:5509061 20150205 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001806 decreased IgM level IEA N RGD:5509061 20150205 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16872848 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12563261 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:15219462 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002360 abnormal spleen B cell corona morphology IAGP N RGD:5509061 20141003 MGI PMID:15219462 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:19100679 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12239221 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11896394 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15219462 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16872848 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15219462 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9586639 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15219462 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002606 increased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20240523 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:15219462 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:15219462 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20181227 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19100679 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:11672542 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12239221 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:15219462 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:9252121 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004798 decreased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004944 abnormal B cell negative selection IAGP N RGD:5509061 20141003 MGI PMID:9586639 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004952 increased spleen weight IEA N RGD:5509061 20181227 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11672542 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004977 increased B-1 B cell number IEA N RGD:5509061 20161201 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:15219462 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563261 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23382690 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9252121 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005018 decreased T cell number IEA N RGD:5509061 20161201 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11896394 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9252121 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20181227 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008171 abnormal mature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9586639 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008202 absent B-1 B cells IAGP N RGD:5509061 20141003 MGI PMID:9586639 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563261 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9252121 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008214 increased immature B cell number IEA N RGD:5509061 20150903 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12563261 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:9586639 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008233 abnormal pro-B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12563261 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:11672542 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:7584145 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:11672542 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:11509585 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:12239221 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0010215 abnormal circulating complement protein level IAGP N RGD:5509061 20141003 MGI PMID:20512127 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0011512 mesangial cell interposition IAGP N RGD:5509061 20141003 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0014350 disorganized spleen B cell follicle IAGP N RGD:5509061 20240104 MGI PMID:19150426 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20150205 MGI 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:23940344 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:19201855 732669 Lyn LYN proto-oncogene, Src family tyrosine kinase gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:23940344 732672 Atox1 antioxidant 1 copper chaperone gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0003067 decreased liver copper level IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0003951 abnormal copper homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0010909 pulmonary alveolar hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11391006 732672 Atox1 antioxidant 1 copper chaperone gene MP:0011215 decreased brain copper level IAGP N RGD:5509061 20141003 MGI PMID:11391006 732675 Fgl2 fibrinogen-like protein 2 gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12840059 732675 Fgl2 fibrinogen-like protein 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:12840059 732675 Fgl2 fibrinogen-like protein 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:15905589 732675 Fgl2 fibrinogen-like protein 2 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0005161 hematuria IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12840059 732675 Fgl2 fibrinogen-like protein 2 gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0013260 decreased dendritic cell apoptosis IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0020153 abnormal urine albumin level IAGP N RGD:5509061 20220616 MGI PMID:18097026 732675 Fgl2 fibrinogen-like protein 2 gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:12840059 732675 Fgl2 fibrinogen-like protein 2 gene MP:0031047 decreased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:12840059 732677 Apoa2 apolipoprotein A-II gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8962133 732677 Apoa2 apolipoprotein A-II gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9186920 732677 Apoa2 apolipoprotein A-II gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:1683229 732677 Apoa2 apolipoprotein A-II gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17485926 732677 Apoa2 apolipoprotein A-II gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:8962133 732677 Apoa2 apolipoprotein A-II gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:8962133 732677 Apoa2 apolipoprotein A-II gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15997185 732677 Apoa2 apolipoprotein A-II gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8962133 732677 Apoa2 apolipoprotein A-II gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8962133 732677 Apoa2 apolipoprotein A-II gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:8962133 732678 Mgat5 mannoside acetylglucosaminyltransferase 5 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:10700233 732678 Mgat5 mannoside acetylglucosaminyltransferase 5 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:10700233 732678 Mgat5 mannoside acetylglucosaminyltransferase 5 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22715095 732678 Mgat5 mannoside acetylglucosaminyltransferase 5 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:10700233 732678 Mgat5 mannoside acetylglucosaminyltransferase 5 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15585841 732678 Mgat5 mannoside acetylglucosaminyltransferase 5 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10700233 732678 Mgat5 mannoside acetylglucosaminyltransferase 5 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:10700233 732678 Mgat5 mannoside acetylglucosaminyltransferase 5 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:10700233 732678 Mgat5 mannoside acetylglucosaminyltransferase 5 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15585841 732678 Mgat5 mannoside acetylglucosaminyltransferase 5 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:15585841 732678 Mgat5 mannoside acetylglucosaminyltransferase 5 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:15585841 732678 Mgat5 mannoside acetylglucosaminyltransferase 5 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15585841 732678 Mgat5 mannoside acetylglucosaminyltransferase 5 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:10700233 732680 Fen1 flap structure specific endonuclease 1 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17283043 732680 Fen1 flap structure specific endonuclease 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:17283043 732680 Fen1 flap structure specific endonuclease 1 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17283043 732680 Fen1 flap structure specific endonuclease 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17283043 732680 Fen1 flap structure specific endonuclease 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:12861020 732680 Fen1 flap structure specific endonuclease 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:12861020 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12119409 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20151119 MGI PMID:24608430 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12119409 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12119409 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002083 premature death IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12861020 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17283043 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17283043 732680 Fen1 flap structure specific endonuclease 1 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:12119409 732680 Fen1 flap structure specific endonuclease 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17283043 732680 Fen1 flap structure specific endonuclease 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20151119 MGI PMID:24608430 732680 Fen1 flap structure specific endonuclease 1 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20151119 MGI PMID:24608430 732680 Fen1 flap structure specific endonuclease 1 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:17283043 732680 Fen1 flap structure specific endonuclease 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0004843 abnormal Paneth cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12119409 732680 Fen1 flap structure specific endonuclease 1 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:12861020 732680 Fen1 flap structure specific endonuclease 1 gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:12861020 732680 Fen1 flap structure specific endonuclease 1 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:12861020 732680 Fen1 flap structure specific endonuclease 1 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12119409 732680 Fen1 flap structure specific endonuclease 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20151119 MGI PMID:24608430 732680 Fen1 flap structure specific endonuclease 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0005631 decreased lung weight IAGP N RGD:5509061 20141003 MGI PMID:17283043 732680 Fen1 flap structure specific endonuclease 1 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20151119 MGI PMID:24608430 732680 Fen1 flap structure specific endonuclease 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20151119 MGI PMID:24608430 732680 Fen1 flap structure specific endonuclease 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:12861020 732680 Fen1 flap structure specific endonuclease 1 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0008404 increased cellular sensitivity to methylmethanesulfonate IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20151119 MGI PMID:24608430 732680 Fen1 flap structure specific endonuclease 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0009246 pale spleen IAGP N RGD:5509061 20141003 MGI PMID:17283043 732680 Fen1 flap structure specific endonuclease 1 gene MP:0009590 increased gonad tumor incidence IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20151119 MGI PMID:24608430 732680 Fen1 flap structure specific endonuclease 1 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12119409 732680 Fen1 flap structure specific endonuclease 1 gene MP:0010365 increased thymus tumor incidence IAGP N RGD:5509061 20151119 MGI PMID:24608430 732680 Fen1 flap structure specific endonuclease 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20151119 MGI PMID:24608430 732680 Fen1 flap structure specific endonuclease 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17283043 732680 Fen1 flap structure specific endonuclease 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16978612 732680 Fen1 flap structure specific endonuclease 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12119409 732680 Fen1 flap structure specific endonuclease 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12861020 732680 Fen1 flap structure specific endonuclease 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:17283043 732680 Fen1 flap structure specific endonuclease 1 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20160609 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20151119 MGI PMID:24608430 732680 Fen1 flap structure specific endonuclease 1 gene MP:0014262 increased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0014347 increased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:18559501 732680 Fen1 flap structure specific endonuclease 1 gene MP:0020414 abnormal fibroblast physiology IAGP N RGD:5509061 20230608 MGI PMID:17283043 732680 Fen1 flap structure specific endonuclease 1 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:17589521 732680 Fen1 flap structure specific endonuclease 1 gene MP:0021086 decreased DNA replication IAGP N RGD:5509061 20220310 MGI PMID:12861020 732680 Fen1 flap structure specific endonuclease 1 gene MP:0030002 increased lung apoptosis IAGP N RGD:5509061 20170629 MGI PMID:17589521 732684 Akr7a5 aldo-keto reductase family 7, member A5 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 732684 Akr7a5 aldo-keto reductase family 7, member A5 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 732684 Akr7a5 aldo-keto reductase family 7, member A5 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:21760938 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:21760938 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:8798738 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21760938 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:8798738 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:8798738 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:8798738 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:8798738 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8798738 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:8798738 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21760938 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:21760938 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:21760938 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8798738 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8798738 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0002658 abnormal liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:9624157 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21760938 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:21760938 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:8798738 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21760938 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8798738 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0005536 decreased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:8798738 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:8798738 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9624157 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21760938 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:8798738 732685 Acox1 acyl-Coenzyme A oxidase 1, palmitoyl gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:9624157 732687 Slc22a7 solute carrier family 22 (organic anion transporter), member 7 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20240523 MGI 732687 Slc22a7 solute carrier family 22 (organic anion transporter), member 7 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20240523 MGI 732687 Slc22a7 solute carrier family 22 (organic anion transporter), member 7 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 732687 Slc22a7 solute carrier family 22 (organic anion transporter), member 7 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 732689 Gzma granzyme A gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:9362539 732689 Gzma granzyme A gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:17919943 732689 Gzma granzyme A gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:12594834 732689 Gzma granzyme A gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:9242702 732689 Gzma granzyme A gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15061770 732689 Gzma granzyme A gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17919943 732689 Gzma granzyme A gene MP:0020943 increased susceptibility to Flaviviridae infection IAGP N RGD:5509061 20200430 MGI PMID:15061770 732690 Defb1 defensin beta 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20231207 MGI 732690 Defb1 defensin beta 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 732690 Defb1 defensin beta 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 732690 Defb1 defensin beta 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12010999 732690 Defb1 defensin beta 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 732690 Defb1 defensin beta 1 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:12010997 732690 Defb1 defensin beta 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12010999 732690 Defb1 defensin beta 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 732693 Lhx5 LIM homeobox protein 5 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220519 MGI 732693 Lhx5 LIM homeobox protein 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 732693 Lhx5 LIM homeobox protein 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 732693 Lhx5 LIM homeobox protein 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 732693 Lhx5 LIM homeobox protein 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 732693 Lhx5 LIM homeobox protein 5 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210520 MGI 732693 Lhx5 LIM homeobox protein 5 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210520 MGI 732693 Lhx5 LIM homeobox protein 5 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:10325223 732693 Lhx5 LIM homeobox protein 5 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:10325223 732693 Lhx5 LIM homeobox protein 5 gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:10325223 732693 Lhx5 LIM homeobox protein 5 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17664423 732693 Lhx5 LIM homeobox protein 5 gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:17664423 732693 Lhx5 LIM homeobox protein 5 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:17664423 732693 Lhx5 LIM homeobox protein 5 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20210520 MGI 732693 Lhx5 LIM homeobox protein 5 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20220519 MGI 732693 Lhx5 LIM homeobox protein 5 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10325223 732693 Lhx5 LIM homeobox protein 5 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210520 MGI 732693 Lhx5 LIM homeobox protein 5 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20210520 MGI 732693 Lhx5 LIM homeobox protein 5 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:10325223 732693 Lhx5 LIM homeobox protein 5 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:10325223 732693 Lhx5 LIM homeobox protein 5 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:10325223 732693 Lhx5 LIM homeobox protein 5 gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:10325223 732693 Lhx5 LIM homeobox protein 5 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:10325223 732693 Lhx5 LIM homeobox protein 5 gene MP:0009324 absent hippocampal fimbria IAGP N RGD:5509061 20141003 MGI PMID:10325223 732693 Lhx5 LIM homeobox protein 5 gene MP:0009718 absent Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:17664423 732693 Lhx5 LIM homeobox protein 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10325223 732693 Lhx5 LIM homeobox protein 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 732694 Mmp12 matrix metallopeptidase 12 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:12634787 732694 Mmp12 matrix metallopeptidase 12 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:16495447 732694 Mmp12 matrix metallopeptidase 12 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:16500946 732694 Mmp12 matrix metallopeptidase 12 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12634787 732694 Mmp12 matrix metallopeptidase 12 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8632994 732694 Mmp12 matrix metallopeptidase 12 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15618213 732694 Mmp12 matrix metallopeptidase 12 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:8632994 732694 Mmp12 matrix metallopeptidase 12 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:14633606 732694 Mmp12 matrix metallopeptidase 12 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:16495447 732694 Mmp12 matrix metallopeptidase 12 gene MP:0031273 decreased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:10841523 732697 Naa35 N(alpha)-acetyltransferase 35, NatC auxiliary subunit gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220811 MGI 732697 Naa35 N(alpha)-acetyltransferase 35, NatC auxiliary subunit gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20230601 MGI 732697 Naa35 N(alpha)-acetyltransferase 35, NatC auxiliary subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16873714 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:19037656 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16873714 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0000492 abnormal rectum morphology IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0000495 abnormal colon morphology IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0000601 small liver IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19037656 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0000706 small thymus IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:15347667 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:16571783 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0002188 small heart IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15347667 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:19037656 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19037656 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:16873714 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20240523 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20240523 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19706538 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16873714 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16873714 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19037656 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:19706538 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:16873714 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16873714 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16873714 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:19037656 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0008850 increased hemoglobin concentration distribution width IAGP N RGD:5509061 20141003 MGI PMID:19037656 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0009531 increased parotid gland size IAGP N RGD:5509061 20141003 MGI PMID:15347667 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0009568 abnormal red blood cell deformability IAGP N RGD:5509061 20141003 MGI PMID:19037656 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0009709 hydrometra IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 732699 Kcnn4 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:19037656 732701 Clstn2 calsyntenin 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 732701 Clstn2 calsyntenin 2 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20171214 MGI PMID:26171716 732701 Clstn2 calsyntenin 2 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20171214 MGI PMID:26171716 732701 Clstn2 calsyntenin 2 gene MP:0020358 abnormal inhibitory synapse morphology IAGP N RGD:5509061 20171214 MGI PMID:26171716 732701 Clstn2 calsyntenin 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:26171716 732703 Cd9 CD9 antigen gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12796480 732703 Cd9 CD9 antigen gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:10634790 732703 Cd9 CD9 antigen gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:10700183 732703 Cd9 CD9 antigen gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20180621 MGI PMID:22609062 732703 Cd9 CD9 antigen gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12796480 732703 Cd9 CD9 antigen gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10634790 732703 Cd9 CD9 antigen gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10634791 732703 Cd9 CD9 antigen gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10700183 732703 Cd9 CD9 antigen gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10634790 732703 Cd9 CD9 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20191205 MGI PMID:31685994 732703 Cd9 CD9 antigen gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:12796480 732703 Cd9 CD9 antigen gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12796480 732703 Cd9 CD9 antigen gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12796480 732703 Cd9 CD9 antigen gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12796480 732703 Cd9 CD9 antigen gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20191205 MGI PMID:31685994 732703 Cd9 CD9 antigen gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:12796480 732703 Cd9 CD9 antigen gene MP:0008976 delayed female fertility IAGP N RGD:5509061 20141003 MGI PMID:10634790 732703 Cd9 CD9 antigen gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20191205 MGI PMID:31685994 732703 Cd9 CD9 antigen gene MP:0030737 decreased glutamic acid level IAGP N RGD:5509061 20191205 MGI PMID:31685994 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20200310 MGI PMID:16478986 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20200310 MGI PMID:19181853 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:12824288 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20200310 MGI PMID:16478986 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20200310 MGI PMID:16478986 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20200310 MGI PMID:16478986 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0002813 microcytosis IAGP N RGD:5509061 20200310 MGI PMID:16478986 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20200310 MGI PMID:16478986 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20200310 MGI PMID:16478986 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20200310 MGI PMID:16478986 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:12606582 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20200310 MGI PMID:12824288 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20200310 MGI PMID:16478986 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0010175 leptocytosis IAGP N RGD:5509061 20200310 MGI PMID:16478986 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0010177 acanthocytosis IAGP N RGD:5509061 20200310 MGI PMID:16478986 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0010178 increased number of Howell-Jolly bodies IAGP N RGD:5509061 20200310 MGI PMID:16478986 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:19181853 732704 Ppp1r15a protein phosphatase 1, regulatory subunit 15A gene MP:0031084 decreased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:16478986 732706 Nlgn2 neuroligin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16982420 732706 Nlgn2 neuroligin 2 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20160414 MGI PMID:25824299 732706 Nlgn2 neuroligin 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20160414 MGI PMID:25824299 732706 Nlgn2 neuroligin 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20190509 MGI PMID:29859117 732706 Nlgn2 neuroligin 2 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20190509 MGI PMID:29859117 732706 Nlgn2 neuroligin 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16982420 732706 Nlgn2 neuroligin 2 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:16982420 732706 Nlgn2 neuroligin 2 gene MP:0002068 abnormal parental behavior IAGP N RGD:5509061 20141003 MGI PMID:16982420 732706 Nlgn2 neuroligin 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:16982420 732706 Nlgn2 neuroligin 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20160414 MGI PMID:25824299 732706 Nlgn2 neuroligin 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20160414 MGI PMID:26291161 732706 Nlgn2 neuroligin 2 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20190509 MGI PMID:29859117 732706 Nlgn2 neuroligin 2 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20190509 MGI PMID:29859117 732706 Nlgn2 neuroligin 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20160414 MGI PMID:25824299 732706 Nlgn2 neuroligin 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20160414 MGI PMID:26291161 732706 Nlgn2 neuroligin 2 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:16982420 732706 Nlgn2 neuroligin 2 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20190509 MGI PMID:29859117 732706 Nlgn2 neuroligin 2 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20160414 MGI PMID:26291161 732706 Nlgn2 neuroligin 2 gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20190509 MGI PMID:29859117 732706 Nlgn2 neuroligin 2 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20190509 MGI PMID:29859117 732706 Nlgn2 neuroligin 2 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20160414 MGI PMID:25824299 732706 Nlgn2 neuroligin 2 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20160414 MGI PMID:26291161 732706 Nlgn2 neuroligin 2 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20190509 MGI PMID:29859117 732706 Nlgn2 neuroligin 2 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20160414 MGI PMID:25824299 732706 Nlgn2 neuroligin 2 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20190509 MGI PMID:29859117 732706 Nlgn2 neuroligin 2 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20160414 MGI PMID:25824299 732706 Nlgn2 neuroligin 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20160414 MGI PMID:25824299 732706 Nlgn2 neuroligin 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20160414 MGI PMID:26291161 732706 Nlgn2 neuroligin 2 gene MP:0010746 abnormal pre-Botzinger complex physiology IAGP N RGD:5509061 20141003 MGI PMID:16982420 732706 Nlgn2 neuroligin 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16982420 732706 Nlgn2 neuroligin 2 gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20160414 MGI PMID:26291161 732706 Nlgn2 neuroligin 2 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20160414 MGI PMID:26291161 732706 Nlgn2 neuroligin 2 gene MP:0012006 abnormal hippocampus physiology IAGP N RGD:5509061 20190509 MGI PMID:29859117 732706 Nlgn2 neuroligin 2 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:25824299 732706 Nlgn2 neuroligin 2 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:26291161 732706 Nlgn2 neuroligin 2 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:29859117 732706 Nlgn2 neuroligin 2 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:25824299 732706 Nlgn2 neuroligin 2 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:26291161 732706 Nlgn2 neuroligin 2 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:29859117 732706 Nlgn2 neuroligin 2 gene MP:0020422 decreased freezing behavior IAGP N RGD:5509061 20190509 MGI PMID:29859117 732706 Nlgn2 neuroligin 2 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20190509 MGI PMID:29859117 732711 Cmklr2 chemerin chemokine-like receptor 2 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20191003 MGI PMID:29793502 732711 Cmklr2 chemerin chemokine-like receptor 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20191003 MGI PMID:29793502 732711 Cmklr2 chemerin chemokine-like receptor 2 gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20191003 MGI PMID:29793502 732711 Cmklr2 chemerin chemokine-like receptor 2 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20191003 MGI PMID:29793502 732711 Cmklr2 chemerin chemokine-like receptor 2 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20191003 MGI PMID:29793502 732711 Cmklr2 chemerin chemokine-like receptor 2 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20191003 MGI PMID:29793502 732711 Cmklr2 chemerin chemokine-like receptor 2 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20191003 MGI PMID:29793502 732712 Rps26 ribosomal protein S26 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20210610 MGI PMID:30451825 732712 Rps26 ribosomal protein S26 gene MP:0001127 small ovary IAGP N RGD:5509061 20210610 MGI PMID:30451825 732712 Rps26 ribosomal protein S26 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220407 MGI PMID:30451825 732712 Rps26 ribosomal protein S26 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20210610 MGI PMID:30451825 732712 Rps26 ribosomal protein S26 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20181227 MGI 732712 Rps26 ribosomal protein S26 gene MP:0001926 female infertility IAGP N RGD:5509061 20210610 MGI PMID:30451825 732712 Rps26 ribosomal protein S26 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20210610 MGI PMID:30451825 732712 Rps26 ribosomal protein S26 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 732712 Rps26 ribosomal protein S26 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20210610 MGI PMID:30451825 732712 Rps26 ribosomal protein S26 gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20210610 MGI PMID:30451825 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15238603 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:20363774 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:19401562 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19401562 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16186188 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19380761 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19380761 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18342008 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0001844 autoimmune response IEA N RGD:5509061 20111116 MGI 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15238603 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:15238603 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20363774 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15238603 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19401562 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18342008 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0002408 abnormal double-positive T cell morphology IEA N RGD:5509061 20111116 MGI 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19401562 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0002444 abnormal T cell physiology IEA N RGD:5509061 20111116 MGI 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0002493 increased IgG level IEA N RGD:5509061 20111116 MGI 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0002497 increased IgE level IEA N RGD:5509061 20111116 MGI 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15238603 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:20363774 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:18342008 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:19380761 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:18342008 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:19401562 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:18342008 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:18342008 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19401562 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:18203684 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20160526 MGI PMID:23162753 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:19401562 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:19401562 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18342008 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19380761 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19401562 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19401562 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:20363774 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16186188 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:18342008 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:18203684 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15238603 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16186188 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19401562 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16186188 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18342008 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19401562 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19380761 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19401562 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19401562 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16186188 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18203684 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19401562 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:20363774 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20160526 MGI PMID:23162753 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15238603 732714 Lcp2 lymphocyte cytosolic protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732719 Grin2d glutamate receptor, ionotropic, NMDA2D (epsilon 4) gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 732719 Grin2d glutamate receptor, ionotropic, NMDA2D (epsilon 4) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:8774946 732719 Grin2d glutamate receptor, ionotropic, NMDA2D (epsilon 4) gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:11488959 732719 Grin2d glutamate receptor, ionotropic, NMDA2D (epsilon 4) gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20141003 MGI 732719 Grin2d glutamate receptor, ionotropic, NMDA2D (epsilon 4) gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:8774946 732719 Grin2d glutamate receptor, ionotropic, NMDA2D (epsilon 4) gene MP:0002834 decreased heart weight IEA N RGD:5509061 20141003 MGI 732719 Grin2d glutamate receptor, ionotropic, NMDA2D (epsilon 4) gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 732719 Grin2d glutamate receptor, ionotropic, NMDA2D (epsilon 4) gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20141003 MGI 732719 Grin2d glutamate receptor, ionotropic, NMDA2D (epsilon 4) gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20141003 MGI 732719 Grin2d glutamate receptor, ionotropic, NMDA2D (epsilon 4) gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20160804 MGI 732721 Trpc6 transient receptor potential cation channel, subfamily C, member 6 gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:16055711 732721 Trpc6 transient receptor potential cation channel, subfamily C, member 6 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20141003 MGI 732721 Trpc6 transient receptor potential cation channel, subfamily C, member 6 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16055711 732721 Trpc6 transient receptor potential cation channel, subfamily C, member 6 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:16055711 732721 Trpc6 transient receptor potential cation channel, subfamily C, member 6 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:21261756 732721 Trpc6 transient receptor potential cation channel, subfamily C, member 6 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:16055711 732722 Prl7d1 prolactin family 7, subfamily d, member 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 732722 Prl7d1 prolactin family 7, subfamily d, member 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20201210 MGI PMID:31012985 732722 Prl7d1 prolactin family 7, subfamily d, member 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20201210 MGI PMID:31012985 732722 Prl7d1 prolactin family 7, subfamily d, member 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20201210 MGI PMID:31012985 732722 Prl7d1 prolactin family 7, subfamily d, member 1 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20201210 MGI PMID:31012985 732722 Prl7d1 prolactin family 7, subfamily d, member 1 gene MP:0008957 abnormal placenta junctional zone morphology IAGP N RGD:5509061 20201210 MGI PMID:31012985 732722 Prl7d1 prolactin family 7, subfamily d, member 1 gene MP:0009394 increased uterine NK cell number IAGP N RGD:5509061 20201210 MGI PMID:31012985 732722 Prl7d1 prolactin family 7, subfamily d, member 1 gene MP:0012108 increased trophoblast glycogen cell number IAGP N RGD:5509061 20201210 MGI PMID:31012985 732722 Prl7d1 prolactin family 7, subfamily d, member 1 gene MP:0012726 abnormal uterine spiral artery morphology IAGP N RGD:5509061 20201210 MGI PMID:31012985 732723 Nbn nibrin gene MP:0000168 abnormal bone marrow development IAGP N RGD:5509061 20211021 MGI PMID:28076792 732723 Nbn nibrin gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20211021 MGI PMID:28076792 732723 Nbn nibrin gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:19171781 732723 Nbn nibrin gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:19171781 732723 Nbn nibrin gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:21147852 732723 Nbn nibrin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11889050 732723 Nbn nibrin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17429352 732723 Nbn nibrin gene MP:0001577 anemia IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:11889050 732723 Nbn nibrin gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11231126 732723 Nbn nibrin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11889050 732723 Nbn nibrin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15668392 732723 Nbn nibrin gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11889050 732723 Nbn nibrin gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11889050 732723 Nbn nibrin gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:11889050 732723 Nbn nibrin gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:11967151 732723 Nbn nibrin gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11889050 732723 Nbn nibrin gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20211021 MGI PMID:28076792 732723 Nbn nibrin gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20211021 MGI PMID:28076792 732723 Nbn nibrin gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20211021 MGI PMID:28076792 732723 Nbn nibrin gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11967151 732723 Nbn nibrin gene MP:0002083 premature death IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11231126 732723 Nbn nibrin gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:19171781 732723 Nbn nibrin gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:11889050 732723 Nbn nibrin gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15668392 732723 Nbn nibrin gene MP:0002583 absent extraembryonic ectoderm IAGP N RGD:5509061 20141003 MGI PMID:11231126 732723 Nbn nibrin gene MP:0002627 increased teratoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11967151 732723 Nbn nibrin gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:11889050 732723 Nbn nibrin gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20211021 MGI PMID:28076792 732723 Nbn nibrin gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:11889050 732723 Nbn nibrin gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0003496 increased thyroid adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20211021 MGI PMID:28076792 732723 Nbn nibrin gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:11231126 732723 Nbn nibrin gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:11967151 732723 Nbn nibrin gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:15333589 732723 Nbn nibrin gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:11967151 732723 Nbn nibrin gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20211021 MGI PMID:28076792 732723 Nbn nibrin gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20211021 MGI PMID:28076792 732723 Nbn nibrin gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17429352 732723 Nbn nibrin gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:19171781 732723 Nbn nibrin gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:11889050 732723 Nbn nibrin gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:11231126 732723 Nbn nibrin gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11889050 732723 Nbn nibrin gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15668392 732723 Nbn nibrin gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:21147852 732723 Nbn nibrin gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17429352 732723 Nbn nibrin gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11889050 732723 Nbn nibrin gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11889050 732723 Nbn nibrin gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11889050 732723 Nbn nibrin gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15668392 732723 Nbn nibrin gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:15668392 732723 Nbn nibrin gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:15668392 732723 Nbn nibrin gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:15668392 732723 Nbn nibrin gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20211021 MGI PMID:28076792 732723 Nbn nibrin gene MP:0009590 increased gonad tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0009591 increased liver adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0009592 increased Leydig cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:11967151 732723 Nbn nibrin gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20211021 MGI PMID:28076792 732723 Nbn nibrin gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19171781 732723 Nbn nibrin gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15333589 732723 Nbn nibrin gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19171781 732723 Nbn nibrin gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20211021 MGI PMID:28076792 732723 Nbn nibrin gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11967151 732723 Nbn nibrin gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11231126 732723 Nbn nibrin gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0011184 absent embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:11231126 732723 Nbn nibrin gene MP:0011198 absent proamniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:11231126 732723 Nbn nibrin gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141120 MGI PMID:11889050 732723 Nbn nibrin gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:11231126 732723 Nbn nibrin gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11967151 732723 Nbn nibrin gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14612522 732723 Nbn nibrin gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15821748 732723 Nbn nibrin gene MP:0013236 ovary degeneration IAGP N RGD:5509061 20141120 MGI PMID:11889050 732723 Nbn nibrin gene MP:0013662 decreased myeloid cell number IAGP N RGD:5509061 20211021 MGI PMID:31285322 732723 Nbn nibrin gene MP:0014049 increased T cell acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20211021 MGI PMID:31285322 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20181018 MGI PMID:24658400 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0001726 abnormal allantois morphology IEA N RGD:5509061 20160811 MGI 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20181018 MGI PMID:24658400 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20181018 MGI PMID:24658400 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20181018 MGI PMID:24658400 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20181018 MGI PMID:24658400 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20181018 MGI PMID:24658400 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20181018 MGI PMID:24658400 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20181018 MGI PMID:24658400 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20181018 MGI PMID:24658400 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 732728 Slc25a3 solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:24658400 732735 Ppm1g protein phosphatase 1G (formerly 2C), magnesium-dependent, gamma isoform gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20111116 MGI 732735 Ppm1g protein phosphatase 1G (formerly 2C), magnesium-dependent, gamma isoform gene MP:0011090 perinatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 732736 Il13ra1 interleukin 13 receptor, alpha 1 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:22351937 732736 Il13ra1 interleukin 13 receptor, alpha 1 gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22351937 732736 Il13ra1 interleukin 13 receptor, alpha 1 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:18066066 732736 Il13ra1 interleukin 13 receptor, alpha 1 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:18066066 732736 Il13ra1 interleukin 13 receptor, alpha 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:18066066 732736 Il13ra1 interleukin 13 receptor, alpha 1 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18066066 732736 Il13ra1 interleukin 13 receptor, alpha 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18066066 732736 Il13ra1 interleukin 13 receptor, alpha 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:18066066 732736 Il13ra1 interleukin 13 receptor, alpha 1 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:18066066 732736 Il13ra1 interleukin 13 receptor, alpha 1 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:18066066 732736 Il13ra1 interleukin 13 receptor, alpha 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18066066 732736 Il13ra1 interleukin 13 receptor, alpha 1 gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:18066066 732736 Il13ra1 interleukin 13 receptor, alpha 1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18066066 732736 Il13ra1 interleukin 13 receptor, alpha 1 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:18066066 732736 Il13ra1 interleukin 13 receptor, alpha 1 gene MP:0008626 increased circulating interleukin-5 level IAGP N RGD:5509061 20141003 MGI PMID:18066066 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210520 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:17045797 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20230601 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230601 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0001725 abnormal umbilical cord morphology IEA N RGD:5509061 20210826 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:17045797 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17045797 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20220811 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14993927 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210826 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20210520 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:17045797 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0006416 abnormal rete testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20141003 MGI PMID:12138202 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 732738 Ncoa2 nuclear receptor coactivator 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 732742 Psmc5 protease (prosome, macropain) 26S subunit, ATPase 5 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20180524 MGI PMID:29217409 732742 Psmc5 protease (prosome, macropain) 26S subunit, ATPase 5 gene MP:0011624 abnormal sensitization to xenobiotic IAGP N RGD:5509061 20180524 MGI PMID:29217409 732744 Has2 hyaluronan synthase 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20221124 MGI PMID:31526805 732744 Has2 hyaluronan synthase 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:19633173 732744 Has2 hyaluronan synthase 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:23313125 732744 Has2 hyaluronan synthase 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:23313125 732744 Has2 hyaluronan synthase 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19633173 732744 Has2 hyaluronan synthase 2 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:19633173 732744 Has2 hyaluronan synthase 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0000296 absent trabeculae carneae IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20221124 MGI PMID:31526805 732744 Has2 hyaluronan synthase 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20221124 MGI PMID:31526805 732744 Has2 hyaluronan synthase 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:19633173 732744 Has2 hyaluronan synthase 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19633173 732744 Has2 hyaluronan synthase 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:23313125 732744 Has2 hyaluronan synthase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20823158 732744 Has2 hyaluronan synthase 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20221124 MGI PMID:31526805 732744 Has2 hyaluronan synthase 2 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:19633173 732744 Has2 hyaluronan synthase 2 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:23313125 732744 Has2 hyaluronan synthase 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19633173 732744 Has2 hyaluronan synthase 2 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0004055 heart atrium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:19633173 732744 Has2 hyaluronan synthase 2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20221124 MGI PMID:31526805 732744 Has2 hyaluronan synthase 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:19633173 732744 Has2 hyaluronan synthase 2 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:19633173 732744 Has2 hyaluronan synthase 2 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:19633173 732744 Has2 hyaluronan synthase 2 gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20141003 MGI PMID:19633173 732744 Has2 hyaluronan synthase 2 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20221124 MGI PMID:31526805 732744 Has2 hyaluronan synthase 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221124 MGI PMID:31526805 732744 Has2 hyaluronan synthase 2 gene MP:0009906 increased tongue size IAGP N RGD:5509061 20221124 MGI PMID:31526805 732744 Has2 hyaluronan synthase 2 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20221124 MGI PMID:31526805 732744 Has2 hyaluronan synthase 2 gene MP:0010655 absent cardiac jelly IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20221124 MGI PMID:31526805 732744 Has2 hyaluronan synthase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:10930438 732744 Has2 hyaluronan synthase 2 gene MP:0011261 abnormal limb mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:23313125 732744 Has2 hyaluronan synthase 2 gene MP:0013818 abnormal oral cavity morphology IAGP N RGD:5509061 20221124 MGI PMID:31526805 732744 Has2 hyaluronan synthase 2 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20221124 MGI PMID:31526805 732744 Has2 hyaluronan synthase 2 gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:23313125 732744 Has2 hyaluronan synthase 2 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:31526805 732744 Has2 hyaluronan synthase 2 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230302 MGI PMID:31526805 732746 Msh2 mutS homolog 2 gene MP:0001577 anemia IAGP N RGD:5509061 20150611 MGI PMID:8674041 732746 Msh2 mutS homolog 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:14568978 732746 Msh2 mutS homolog 2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:10369687 732746 Msh2 mutS homolog 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10992298 732746 Msh2 mutS homolog 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 732746 Msh2 mutS homolog 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14744764 732746 Msh2 mutS homolog 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 732746 Msh2 mutS homolog 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22447450 732746 Msh2 mutS homolog 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 732746 Msh2 mutS homolog 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7628020 732746 Msh2 mutS homolog 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 732746 Msh2 mutS homolog 2 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 732746 Msh2 mutS homolog 2 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 732746 Msh2 mutS homolog 2 gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 732746 Msh2 mutS homolog 2 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:12531021 732746 Msh2 mutS homolog 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10992298 732746 Msh2 mutS homolog 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12234974 732746 Msh2 mutS homolog 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12531021 732746 Msh2 mutS homolog 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14744764 732746 Msh2 mutS homolog 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15126346 732746 Msh2 mutS homolog 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15700306 732746 Msh2 mutS homolog 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19931261 732746 Msh2 mutS homolog 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22447450 732746 Msh2 mutS homolog 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7550317 732746 Msh2 mutS homolog 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9443401 732746 Msh2 mutS homolog 2 gene MP:0002083 premature death IAGP N RGD:5509061 20150611 MGI PMID:8674041 732746 Msh2 mutS homolog 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12234974 732746 Msh2 mutS homolog 2 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19931261 732746 Msh2 mutS homolog 2 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20150611 MGI PMID:8674041 732746 Msh2 mutS homolog 2 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14568978 732746 Msh2 mutS homolog 2 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14744764 732746 Msh2 mutS homolog 2 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19931261 732746 Msh2 mutS homolog 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:15533840 732746 Msh2 mutS homolog 2 gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:10992298 732746 Msh2 mutS homolog 2 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20150611 MGI PMID:8674041 732746 Msh2 mutS homolog 2 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10992298 732746 Msh2 mutS homolog 2 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:12234974 732746 Msh2 mutS homolog 2 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:19931261 732746 Msh2 mutS homolog 2 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 732746 Msh2 mutS homolog 2 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 732746 Msh2 mutS homolog 2 gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12531021 732746 Msh2 mutS homolog 2 gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:12554681 732746 Msh2 mutS homolog 2 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 732746 Msh2 mutS homolog 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:9443401 732746 Msh2 mutS homolog 2 gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:12531021 732746 Msh2 mutS homolog 2 gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20141003 MGI PMID:19901081 732746 Msh2 mutS homolog 2 gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20220721 MGI PMID:34819670 732746 Msh2 mutS homolog 2 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:10369687 732746 Msh2 mutS homolog 2 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:10430621 732746 Msh2 mutS homolog 2 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:14568978 732746 Msh2 mutS homolog 2 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20220721 MGI PMID:34819670 732746 Msh2 mutS homolog 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12531017 732746 Msh2 mutS homolog 2 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 732746 Msh2 mutS homolog 2 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20150611 MGI PMID:23741483 732746 Msh2 mutS homolog 2 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 732746 Msh2 mutS homolog 2 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 732746 Msh2 mutS homolog 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10430621 732746 Msh2 mutS homolog 2 gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:15533840 732746 Msh2 mutS homolog 2 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:10369687 732746 Msh2 mutS homolog 2 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:10369687 732746 Msh2 mutS homolog 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:14744764 732746 Msh2 mutS homolog 2 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19931261 732746 Msh2 mutS homolog 2 gene MP:0009222 increased uterus tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 732746 Msh2 mutS homolog 2 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 732746 Msh2 mutS homolog 2 gene MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19931261 732746 Msh2 mutS homolog 2 gene MP:0009320 increased lymphoblastic lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 732746 Msh2 mutS homolog 2 gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12531021 732746 Msh2 mutS homolog 2 gene MP:0009797 abnormal mismatch repair IAGP N RGD:5509061 20141003 MGI PMID:14744764 732746 Msh2 mutS homolog 2 gene MP:0009797 abnormal mismatch repair IAGP N RGD:5509061 20141003 MGI PMID:19931261 732746 Msh2 mutS homolog 2 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:14744764 732746 Msh2 mutS homolog 2 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10992298 732746 Msh2 mutS homolog 2 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 732746 Msh2 mutS homolog 2 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19931261 732746 Msh2 mutS homolog 2 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 732746 Msh2 mutS homolog 2 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 732746 Msh2 mutS homolog 2 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 732746 Msh2 mutS homolog 2 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12531021 732746 Msh2 mutS homolog 2 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 732746 Msh2 mutS homolog 2 gene MP:0010345 increased thyroid C-cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 732746 Msh2 mutS homolog 2 gene MP:0010350 increased pituitary adenohypophysis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 732746 Msh2 mutS homolog 2 gene MP:0010351 increased pituitary melanotroph tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12234974 732746 Msh2 mutS homolog 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19805137 732746 Msh2 mutS homolog 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22447450 732746 Msh2 mutS homolog 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10992298 732746 Msh2 mutS homolog 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12531021 732746 Msh2 mutS homolog 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14568978 732746 Msh2 mutS homolog 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14744764 732746 Msh2 mutS homolog 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 732746 Msh2 mutS homolog 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15700306 732746 Msh2 mutS homolog 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19931261 732746 Msh2 mutS homolog 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22447450 732746 Msh2 mutS homolog 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:7550317 732746 Msh2 mutS homolog 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9443401 732746 Msh2 mutS homolog 2 gene MP:0014234 decreased enterocyte apoptosis IAGP N RGD:5509061 20230323 MGI PMID:10097137 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20141003 MGI 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:9207786 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9207786 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9207786 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0002332 abnormal exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:9207786 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0002833 increased heart weight IEA N RGD:5509061 20141003 MGI 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20201231 MGI 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20141003 MGI 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20150108 MGI 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9207786 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:14749836 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:9207786 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:9207786 732749 Slc25a4 solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene MP:0030673 increased circulating alanine level IAGP N RGD:5509061 20180920 MGI PMID:9207786 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0001619 abnormal vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:24485460 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20170413 MGI PMID:27814941 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20210708 MGI PMID:32868928 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20170413 MGI PMID:27814941 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20210708 MGI PMID:32868928 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0009671 abnormal uterus physiology IAGP N RGD:5509061 20141003 MGI PMID:24485460 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17515897 732752 Nr4a1 nuclear receptor subfamily 4, group A, member 1 gene MP:0013026 decreased Ly6C low monocyte number IAGP N RGD:5509061 20170413 MGI PMID:27814941 732755 Vps45 vacuolar protein sorting 45 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20221215 MGI PMID:33512427 732755 Vps45 vacuolar protein sorting 45 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20221215 MGI PMID:33512427 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:12595342 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:20442405 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20442405 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:7566154 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16374517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7566154 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:16391003 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:16247468 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:16247468 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:16247468 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:16247468 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:20442405 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000597 delayed hepatic development IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8562954 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:16247468 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:15967814 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20442405 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23255596 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12595342 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16391003 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20530207 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16374517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:7566154 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:7566154 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:7566154 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12595342 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15967814 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16391003 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20530207 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:12595342 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:16391003 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15967814 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20530207 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12595342 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15967814 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16391003 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20442405 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20530207 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8562954 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23255596 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:18279360 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:16374517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:16374517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0002763 ectopic Bergmann glia cells IAGP N RGD:5509061 20141003 MGI PMID:18279360 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:7566154 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:20530207 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:7566154 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:15967814 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15967814 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16391003 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20442405 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20530207 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:15967814 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:20530207 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:15601818 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23255596 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:23255596 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003542 abnormal vascular endothelial cell development IAGP N RGD:5509061 20141003 MGI PMID:12595342 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:15967814 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:16391003 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003894 abnormal Purkinje cell innervation IAGP N RGD:5509061 20141003 MGI PMID:18279360 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:7566154 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15967814 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:20442405 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:20442405 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15601818 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:20442405 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12595342 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:7566154 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:20530207 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:15967814 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:8562954 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:7566154 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16374517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16391003 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16374517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20442405 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20530207 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15967814 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16391003 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:20442405 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18669633 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15601818 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16247468 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:20442405 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:18279360 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0010547 abnormal mesocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:7566154 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0010656 thick myocardium IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0010664 abnormal vitelline artery morphology IAGP N RGD:5509061 20141003 MGI PMID:7566154 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20442405 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12595342 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15967814 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16391003 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20442405 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20530207 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20530207 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15967814 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011201 abnormal visceral yolk sac cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011257 abnormal head fold morphology IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:15967814 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:20530207 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011706 abnormal fibroblast migration IAGP N RGD:5509061 20141003 MGI PMID:20442405 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:19776009 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0012104 small amniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0012131 small visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:7478517 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0012194 decreased keratinocyte migration IAGP N RGD:5509061 20141204 MGI PMID:15601818 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0013192 decreased sebaceous gland number IAGP N RGD:5509061 20141127 MGI PMID:16247468 732758 Ptk2 PTK2 protein tyrosine kinase 2 gene MP:0013585 thymus cortex atrophy IAGP N RGD:5509061 20150319 MGI PMID:8562954 732761 Dgka diacylglycerol kinase, alpha gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 732761 Dgka diacylglycerol kinase, alpha gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17028587 732761 Dgka diacylglycerol kinase, alpha gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:17028587 732761 Dgka diacylglycerol kinase, alpha gene MP:0005004 abnormal lymphocyte anergy IAGP N RGD:5509061 20141003 MGI PMID:17028587 732761 Dgka diacylglycerol kinase, alpha gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17028587 732761 Dgka diacylglycerol kinase, alpha gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17028587 732762 Lrpap1 low density lipoprotein receptor-related protein associated protein 1 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:16306127 732762 Lrpap1 low density lipoprotein receptor-related protein associated protein 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10363810 732762 Lrpap1 low density lipoprotein receptor-related protein associated protein 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:7538675 732762 Lrpap1 low density lipoprotein receptor-related protein associated protein 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:7538675 732762 Lrpap1 low density lipoprotein receptor-related protein associated protein 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10529267 732762 Lrpap1 low density lipoprotein receptor-related protein associated protein 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:12748857 732762 Lrpap1 low density lipoprotein receptor-related protein associated protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15082773 732762 Lrpap1 low density lipoprotein receptor-related protein associated protein 1 gene MP:0002876 abnormal thyroid gland physiology IAGP N RGD:5509061 20141003 MGI PMID:16306127 732762 Lrpap1 low density lipoprotein receptor-related protein associated protein 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:12417655 732762 Lrpap1 low density lipoprotein receptor-related protein associated protein 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:12417655 732762 Lrpap1 low density lipoprotein receptor-related protein associated protein 1 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10363810 732762 Lrpap1 low density lipoprotein receptor-related protein associated protein 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7538675 732762 Lrpap1 low density lipoprotein receptor-related protein associated protein 1 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:7538675 732762 Lrpap1 low density lipoprotein receptor-related protein associated protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20150129 MGI PMID:7538675 732762 Lrpap1 low density lipoprotein receptor-related protein associated protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10529267 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15148336 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:15148336 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:15749852 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:17404294 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15148336 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16424207 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:15749852 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:15882434 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:17404294 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:15148336 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:15882434 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:15749852 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:15498041 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17404294 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:15749852 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:17404294 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:17404294 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:17404294 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:17404294 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0008552 abnormal circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15148336 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:12270724 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0008595 abnormal circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:15148336 732763 Mbl1 mannose-binding lectin (protein A) 1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12270724 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0000054 delayed ear emergence IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:14996991 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0003280 urinary incontinence IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20150910 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0006276 abnormal autonomic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0009646 urinary bladder inflammation IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210826 MGI 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:10771006 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10531434 732765 Chrnb4 cholinergic receptor, nicotinic, beta polypeptide 4 gene MP:0011625 cystolithiasis IAGP N RGD:5509061 20141003 MGI PMID:10531434 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23143307 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23143307 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12615700 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:23143307 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15126346 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10557315 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:23143307 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:23143307 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10725358 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12874039 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:10725358 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:12874039 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:23143307 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:23143307 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12615700 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:23143307 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0010947 abnormal single-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:23143307 732766 Ogg1 8-oxoguanine DNA-glycosylase 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15126346 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:17626790 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:17626790 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15284456 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:22474261 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:22474261 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17626790 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:15284456 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:15284456 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:22474261 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17626790 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:15284456 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20424607 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:15284456 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17418524 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:15284456 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141009 MGI PMID:24361012 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17418524 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22474261 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:20424607 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17626790 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:17626790 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:17626790 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141009 MGI PMID:24361012 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:17626790 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17626790 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20424607 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:15284456 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141009 MGI PMID:24361012 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:22474261 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:22474261 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141009 MGI PMID:24361012 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17626790 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:22474261 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:20424607 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15284456 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:20424607 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141009 MGI PMID:24361012 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141009 MGI PMID:24361012 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:22474261 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141009 MGI PMID:24361012 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:17626790 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141009 MGI PMID:24361012 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141009 MGI PMID:24361012 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20141003 MGI PMID:17626790 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20424607 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15284456 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17418524 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0011171 increased number of Heinz bodies IAGP N RGD:5509061 20141003 MGI PMID:17626790 732768 Ago2 argonaute RISC catalytic subunit 2 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20141009 MGI PMID:24361012 732769 Cd93 CD93 antigen gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:15004139 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20240523 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20200514 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0000599 enlarged liver IEA N RGD:5509061 20200514 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200514 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20200514 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20220519 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0001523 impaired righting response IEA N RGD:5509061 20201022 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15040800 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20230330 MGI PMID:23180829 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20230330 MGI PMID:23180829 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0001925 male infertility IAGP N RGD:5509061 20230330 MGI PMID:23180829 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0001926 female infertility IAGP N RGD:5509061 20230330 MGI PMID:23180829 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0002139 abnormal hepatobiliary system physiology IAGP N RGD:5509061 20141003 MGI PMID:15040800 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20200514 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20200514 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0002645 abnormal intestinal cholesterol absorption IAGP N RGD:5509061 20150101 MGI PMID:25378657 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20200514 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20200514 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20150101 MGI PMID:25378657 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20150101 MGI PMID:25378657 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20150101 MGI PMID:25378657 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20211021 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20150101 MGI PMID:25378657 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15040800 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20150101 MGI PMID:25378657 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20200514 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20210520 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20200514 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15040800 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20150101 MGI PMID:25378657 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20201022 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0005387 immune system phenotype IEA N RGD:5509061 20210520 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20200514 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210128 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20200514 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20211021 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20211021 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20211021 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20210520 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20210520 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0008207 decreased B-2 B cell number IEA N RGD:5509061 20210520 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20230330 MGI PMID:23180829 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20200514 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0010076 abnormal phytosterol level IAGP N RGD:5509061 20150101 MGI PMID:25378657 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0010077 increased phytosterol level IAGP N RGD:5509061 20150101 MGI PMID:25378657 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0010078 increased circulating phytosterol level IAGP N RGD:5509061 20141003 MGI PMID:15040800 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0010078 increased circulating phytosterol level IAGP N RGD:5509061 20150101 MGI PMID:25378657 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0011044 increased lung elastance IEA N RGD:5509061 20210826 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0013437 decreased phytosterol level IAGP N RGD:5509061 20150101 MGI PMID:25378657 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0013510 decreased CD4-negative NK T cell number IEA N RGD:5509061 20210520 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0013513 decreased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20210520 MGI 732771 Abcg8 ATP binding cassette subfamily G member 8 gene MP:0013756 increased intestinal phytosterol absorption IAGP N RGD:5509061 20200102 MGI PMID:25378657 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:14757745 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:14757745 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12145814 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0001714 absent trophoblast giant cells IAGP N RGD:5509061 20141003 MGI PMID:11084331 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14699085 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11084331 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14699085 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14757745 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:14699085 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:11084331 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:11084331 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:14757745 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11084331 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:11084331 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0003706 abnormal cell nucleus count IAGP N RGD:5509061 20141003 MGI PMID:11084331 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0003708 binucleate IAGP N RGD:5509061 20141003 MGI PMID:11084331 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:11084331 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:14699085 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:14757745 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:14699085 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14699085 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:12145814 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14757745 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14757745 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:14757745 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:11084331 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20141003 MGI PMID:12145814 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12145814 732772 Birc5 baculoviral IAP repeat-containing 5 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11084331 732773 Xylt1 xylosyltransferase 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 732773 Xylt1 xylosyltransferase 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 732773 Xylt1 xylosyltransferase 1 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20231207 MGI 732773 Xylt1 xylosyltransferase 1 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 732773 Xylt1 xylosyltransferase 1 gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 732773 Xylt1 xylosyltransferase 1 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0003416 premature bone ossification IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20231207 MGI 732773 Xylt1 xylosyltransferase 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0003854 abnormal forelimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0003856 abnormal hindlimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201022 MGI 732773 Xylt1 xylosyltransferase 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0010932 increased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0010971 abnormal periosteum morphology IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732773 Xylt1 xylosyltransferase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0014288 rhizomelic limb IAGP N RGD:5509061 20230824 MGI PMID:24161523 732773 Xylt1 xylosyltransferase 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 732778 Pgam2 phosphoglycerate mutase 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20160630 MGI PMID:24929853 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0000767 abnormal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0003622 ischuria IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0009483 enlarged ileum IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0009536 abnormal interstitial cell of Cajal morphology IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16145842 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0011874 enlarged urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:23499953 732779 Ppp1r12a protein phosphatase 1, regulatory subunit 12A gene MP:0011882 enlarged duodenum IAGP N RGD:5509061 20141003 MGI PMID:23499953 732781 Mat2a methionine adenosyltransferase 2A gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20141003 MGI 732781 Mat2a methionine adenosyltransferase 2A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732782 Nkg7 natural killer cell group 7 sequence gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20210318 MGI PMID:32839608 732782 Nkg7 natural killer cell group 7 sequence gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20221215 MGI 732782 Nkg7 natural killer cell group 7 sequence gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 732782 Nkg7 natural killer cell group 7 sequence gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20210318 MGI PMID:32839608 732782 Nkg7 natural killer cell group 7 sequence gene MP:0008087 decreased T helper 1 cell number IAGP N RGD:5509061 20210318 MGI PMID:32839608 732782 Nkg7 natural killer cell group 7 sequence gene MP:0008247 abnormal mononuclear cell morphology IAGP N RGD:5509061 20210318 MGI PMID:32839608 732782 Nkg7 natural killer cell group 7 sequence gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20210318 MGI PMID:32839608 732782 Nkg7 natural killer cell group 7 sequence gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20210318 MGI PMID:32839608 732782 Nkg7 natural killer cell group 7 sequence gene MP:0010750 increased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20210318 MGI PMID:32839608 732782 Nkg7 natural killer cell group 7 sequence gene MP:0010751 decreased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20210318 MGI PMID:32839608 732784 Kl klotho gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11095966 732784 Kl klotho gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:10430604 732784 Kl klotho gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:14528024 732784 Kl klotho gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:12446599 732784 Kl klotho gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10430604 732784 Kl klotho gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:14528024 732784 Kl klotho gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:10430604 732784 Kl klotho gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10615062 732784 Kl klotho gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22878961 732784 Kl klotho gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11016890 732784 Kl klotho gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11095966 732784 Kl klotho gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:14528024 732784 Kl klotho gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:21427221 732784 Kl klotho gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:22878961 732784 Kl klotho gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:12054604 732784 Kl klotho gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15037532 732784 Kl klotho gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:10615062 732784 Kl klotho gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:21427221 732784 Kl klotho gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0000521 abnormal kidney cortex morphology IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:11095966 732784 Kl klotho gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0000692 small spleen IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0000767 abnormal smooth muscle morphology IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:10615062 732784 Kl klotho gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0001218 thin epidermis IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:10615062 732784 Kl klotho gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12446599 732784 Kl klotho gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14528024 732784 Kl klotho gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21427221 732784 Kl klotho gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22878961 732784 Kl klotho gene MP:0001265 decreased body size IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141204 MGI PMID:24045987 732784 Kl klotho gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22878961 732784 Kl klotho gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0001429 dehydration IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12475907 732784 Kl klotho gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12475907 732784 Kl klotho gene MP:0001505 hunched posture IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15037532 732784 Kl klotho gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:14528024 732784 Kl klotho gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:21427221 732784 Kl klotho gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:22878961 732784 Kl klotho gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11095966 732784 Kl klotho gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12475907 732784 Kl klotho gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14528024 732784 Kl klotho gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22878961 732784 Kl klotho gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11095966 732784 Kl klotho gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:14528024 732784 Kl klotho gene MP:0001861 lung inflammation IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0001914 hemorrhage IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0001954 respiratory distress IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:10615062 732784 Kl klotho gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:21427221 732784 Kl klotho gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0001958 emphysema IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11095966 732784 Kl klotho gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12475907 732784 Kl klotho gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14528024 732784 Kl klotho gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15037532 732784 Kl klotho gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21427221 732784 Kl klotho gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22878961 732784 Kl klotho gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0002083 premature death IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0002123 abnormal definitive hematopoiesis IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:22878961 732784 Kl klotho gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:10615062 732784 Kl klotho gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20141003 MGI PMID:10615062 732784 Kl klotho gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11016890 732784 Kl klotho gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11095966 732784 Kl klotho gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 732784 Kl klotho gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11016890 732784 Kl klotho gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11095966 732784 Kl klotho gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:22878961 732784 Kl klotho gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:22878961 732784 Kl klotho gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:22878961 732784 Kl klotho gene MP:0003014 abnormal kidney medulla morphology IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:11016890 732784 Kl klotho gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20150611 MGI PMID:9363890 732784 Kl klotho gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:12446599 732784 Kl klotho gene MP:0003109 short femur IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 732784 Kl klotho gene MP:0003120 abnormal tracheal cartilage morphology IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0003195 calcinosis IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0003195 calcinosis IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0003196 calcified skin IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0003196 calcified skin IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:21427221 732784 Kl klotho gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:22878961 732784 Kl klotho gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0003199 calcified muscle IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:11095966 732784 Kl klotho gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12475907 732784 Kl klotho gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:12475907 732784 Kl klotho gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:15037532 732784 Kl klotho gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0003924 diaphragmatic hernia IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0003946 renal necrosis IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22878961 732784 Kl klotho gene MP:0003991 arteriosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15037532 732784 Kl klotho gene MP:0003991 arteriosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0004676 wide ribs IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0004692 small pubis IAGP N RGD:5509061 20210930 MGI PMID:33905568 732784 Kl klotho gene MP:0004754 abnormal kidney collecting duct morphology IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0004894 uterus atrophy IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:10430604 732784 Kl klotho gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:12446599 732784 Kl klotho gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:10430604 732784 Kl klotho gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:10430604 732784 Kl klotho gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20220915 MGI PMID:10430604 732784 Kl klotho gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:10430604 732784 Kl klotho gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12446599 732784 Kl klotho gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11095966 732784 Kl klotho gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11095966 732784 Kl klotho gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15037532 732784 Kl klotho gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:22878961 732784 Kl klotho gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:11095966 732784 Kl klotho gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0005586 decreased tidal volume IAGP N RGD:5509061 20141003 MGI PMID:10615062 732784 Kl klotho gene MP:0005665 increased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:15037532 732784 Kl klotho gene MP:0006133 calcified artery IAGP N RGD:5509061 20141003 MGI PMID:21427221 732784 Kl klotho gene MP:0006133 calcified artery IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:15037532 732784 Kl klotho gene MP:0006325 impaired hearing IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0006357 abnormal circulating mineral level IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0008325 abnormal gonadotroph morphology IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0008373 short malleus IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0008374 abnormal malleus manubrium morphology IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0008375 short malleus manubrium IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0008417 decreased somatotroph cell size IAGP N RGD:5509061 20150129 MGI PMID:9363890 732784 Kl klotho gene MP:0008436 decreased somatotroph secretory granule number IAGP N RGD:5509061 20150129 MGI PMID:9363890 732784 Kl klotho gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:11095966 732784 Kl klotho gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:11095966 732784 Kl klotho gene MP:0009201 external male genitalia atrophy IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0009212 vulva atrophy IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15037532 732784 Kl klotho gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0010119 abnormal bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:10430604 732784 Kl klotho gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20141003 MGI PMID:15037532 732784 Kl klotho gene MP:0010522 calcified aorta IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0010522 calcified aorta IAGP N RGD:5509061 20201112 MGI PMID:9363890 732784 Kl klotho gene MP:0010870 absent bone trabeculae IEA N RGD:5509061 20141003 MGI 732784 Kl klotho gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:10615062 732784 Kl klotho gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20141003 MGI PMID:10615062 732784 Kl klotho gene MP:0010908 dilated pulmonary alveolar duct IAGP N RGD:5509061 20141003 MGI PMID:10615062 732784 Kl klotho gene MP:0010923 calcified pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:10615062 732784 Kl klotho gene MP:0010923 calcified pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:9363890 732784 Kl klotho gene MP:0010923 calcified pulmonary alveolus IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:14528024 732784 Kl klotho gene MP:0011360 kidney cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22878961 732784 Kl klotho gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20141204 MGI PMID:24045987 732784 Kl klotho gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20141204 MGI PMID:24045987 732784 Kl klotho gene MP:0012151 increased a-wave latency IAGP N RGD:5509061 20141204 MGI PMID:24045987 732784 Kl klotho gene MP:0012153 increased b-wave latency IAGP N RGD:5509061 20141204 MGI PMID:24045987 732784 Kl klotho gene MP:0012337 increased vitamin D level IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0013566 dilated gastric gland IEA N RGD:5509061 20150312 MGI 732784 Kl klotho gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20170713 MGI PMID:25860694 732784 Kl klotho gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20220915 MGI PMID:10430604 732784 Kl klotho gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:12475907 732784 Kl klotho gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:10430604 732784 Kl klotho gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:25860694 732784 Kl klotho gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20220915 MGI PMID:10430604 732784 Kl klotho gene MP:0030376 thick zygomatic arch IAGP N RGD:5509061 20171207 MGI PMID:25860694 732784 Kl klotho gene MP:0030405 small stapes obturator foramen IAGP N RGD:5509061 20171207 MGI PMID:25860694 732784 Kl klotho gene MP:0030584 skin atrophy IAGP N RGD:5509061 20180614 MGI PMID:25860694 732784 Kl klotho gene MP:0031519 calcified aortic valve annulus IAGP N RGD:5509061 20240104 MGI PMID:15037532 732784 Kl klotho gene MP:0031521 calcified mitral valve annulus IAGP N RGD:5509061 20240104 MGI PMID:15037532 732786 Serp1 stress-associated endoplasmic reticulum protein 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16705175 732786 Serp1 stress-associated endoplasmic reticulum protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16705175 732786 Serp1 stress-associated endoplasmic reticulum protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16705175 732786 Serp1 stress-associated endoplasmic reticulum protein 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16705175 732786 Serp1 stress-associated endoplasmic reticulum protein 1 gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:16705175 732786 Serp1 stress-associated endoplasmic reticulum protein 1 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:16705175 732786 Serp1 stress-associated endoplasmic reticulum protein 1 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:16705175 732786 Serp1 stress-associated endoplasmic reticulum protein 1 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:16705175 732786 Serp1 stress-associated endoplasmic reticulum protein 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16705175 732786 Serp1 stress-associated endoplasmic reticulum protein 1 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:16705175 732786 Serp1 stress-associated endoplasmic reticulum protein 1 gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:16705175 732786 Serp1 stress-associated endoplasmic reticulum protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16705175 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20111116 MGI 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15383666 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0001805 decreased IgG level IEA N RGD:5509061 20111116 MGI 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20180927 MGI PMID:29867208 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20180927 MGI PMID:29867208 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20180927 MGI PMID:29867208 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0003954 abnormal Reichert's membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:15383666 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20180927 MGI PMID:29867208 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0005590 increased vasodilation IEA N RGD:5509061 20111116 MGI 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20180927 MGI PMID:29867208 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20180927 MGI PMID:29867208 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20180927 MGI PMID:29867208 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20180927 MGI PMID:29867208 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20180927 MGI PMID:29867208 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20180927 MGI PMID:29867208 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15383666 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20180927 MGI PMID:29867208 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0012150 increased b-wave implicit time IAGP N RGD:5509061 20180927 MGI PMID:29867208 732789 Pomt1 protein-O-mannosyltransferase 1 gene MP:0020359 abnormal ribbon synapse morphology IAGP N RGD:5509061 20180927 MGI PMID:29867208 732791 Lmna lamin A gene MP:0000021 prominent ears IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20180222 MGI PMID:22819531 732791 Lmna lamin A gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18769635 732791 Lmna lamin A gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:21088111 732791 Lmna lamin A gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0000066 osteoporosis IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:10579712 732791 Lmna lamin A gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:18769635 732791 Lmna lamin A gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:18769635 732791 Lmna lamin A gene MP:0000160 kyphosis IAGP N RGD:5509061 20220721 MGI PMID:29703891 732791 Lmna lamin A gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15972724 732791 Lmna lamin A gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20181129 MGI PMID:12748643 732791 Lmna lamin A gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:20376364 732791 Lmna lamin A gene MP:0000469 abnormal esophageal squamous epithelium morphology IAGP N RGD:5509061 20160407 MGI PMID:25652409 732791 Lmna lamin A gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20160407 MGI PMID:25652409 732791 Lmna lamin A gene MP:0000585 kinked tail IAGP N RGD:5509061 20160616 MGI PMID:25578479 732791 Lmna lamin A gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:10579712 732791 Lmna lamin A gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:15608054 732791 Lmna lamin A gene MP:0000747 muscle weakness IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:10579712 732791 Lmna lamin A gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:10579712 732791 Lmna lamin A gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20160616 MGI PMID:25578479 732791 Lmna lamin A gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:11799477 732791 Lmna lamin A gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20160407 MGI PMID:25652409 732791 Lmna lamin A gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20160407 MGI PMID:25652409 732791 Lmna lamin A gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:14996939 732791 Lmna lamin A gene MP:0001147 small testis IAGP N RGD:5509061 20151126 MGI PMID:23382700 732791 Lmna lamin A gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:14996939 732791 Lmna lamin A gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0001260 increased body weight IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10579712 732791 Lmna lamin A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18757838 732791 Lmna lamin A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18769635 732791 Lmna lamin A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20421363 732791 Lmna lamin A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21088111 732791 Lmna lamin A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23998933 732791 Lmna lamin A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160616 MGI PMID:25578479 732791 Lmna lamin A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200514 MGI PMID:31833196 732791 Lmna lamin A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220721 MGI PMID:29703891 732791 Lmna lamin A gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18769635 732791 Lmna lamin A gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0001263 weight loss IAGP N RGD:5509061 20160407 MGI PMID:25652409 732791 Lmna lamin A gene MP:0001263 weight loss IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0001265 decreased body size IAGP N RGD:5509061 20160407 MGI PMID:25652409 732791 Lmna lamin A gene MP:0001265 decreased body size IAGP N RGD:5509061 20160616 MGI PMID:25578479 732791 Lmna lamin A gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20240523 MGI 732791 Lmna lamin A gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15972724 732791 Lmna lamin A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10579712 732791 Lmna lamin A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160616 MGI PMID:25578479 732791 Lmna lamin A gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0001443 poor grooming IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0001505 hunched posture IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:15972724 732791 Lmna lamin A gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20180222 MGI PMID:22819531 732791 Lmna lamin A gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10579712 732791 Lmna lamin A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15608054 732791 Lmna lamin A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15972724 732791 Lmna lamin A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23998933 732791 Lmna lamin A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160616 MGI PMID:25578479 732791 Lmna lamin A gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:10579712 732791 Lmna lamin A gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20180222 MGI PMID:22819531 732791 Lmna lamin A gene MP:0001921 reduced fertility IAGP N RGD:5509061 20220721 MGI PMID:29703891 732791 Lmna lamin A gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220721 MGI PMID:29703891 732791 Lmna lamin A gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0001925 male infertility IAGP N RGD:5509061 20151126 MGI PMID:23382700 732791 Lmna lamin A gene MP:0001926 female infertility IAGP N RGD:5509061 20220721 MGI PMID:29703891 732791 Lmna lamin A gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20151126 MGI PMID:23382700 732791 Lmna lamin A gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11855819 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10579712 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15608054 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15972724 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18757838 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18769635 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20421363 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21088111 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21875900 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20160407 MGI PMID:25652409 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20170907 MGI PMID:26436652 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20200514 MGI PMID:31833196 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0002083 premature death IAGP N RGD:5509061 20220721 MGI PMID:29703891 732791 Lmna lamin A gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20180222 MGI PMID:22819531 732791 Lmna lamin A gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21088111 732791 Lmna lamin A gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20151126 MGI PMID:23382700 732791 Lmna lamin A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16511604 732791 Lmna lamin A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23998933 732791 Lmna lamin A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25578479 732791 Lmna lamin A gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0002251 abnormal nasopharynx morphology IAGP N RGD:5509061 20180222 MGI PMID:22819531 732791 Lmna lamin A gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11855819 732791 Lmna lamin A gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11799477 732791 Lmna lamin A gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:15972724 732791 Lmna lamin A gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220721 MGI PMID:29703891 732791 Lmna lamin A gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0002750 exophthalmos IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:20421363 732791 Lmna lamin A gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20170824 MGI PMID:22773734 732791 Lmna lamin A gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20170907 MGI PMID:26436652 732791 Lmna lamin A gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 732791 Lmna lamin A gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15972724 732791 Lmna lamin A gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:20421363 732791 Lmna lamin A gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170824 MGI PMID:22773734 732791 Lmna lamin A gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170907 MGI PMID:26436652 732791 Lmna lamin A gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141030 MGI PMID:23690466 732791 Lmna lamin A gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:21464947 732791 Lmna lamin A gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:10579712 732791 Lmna lamin A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16014412 732791 Lmna lamin A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18757838 732791 Lmna lamin A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18769635 732791 Lmna lamin A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:20421363 732791 Lmna lamin A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:20439468 732791 Lmna lamin A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:21088111 732791 Lmna lamin A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:21464947 732791 Lmna lamin A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:21875900 732791 Lmna lamin A gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20421363 732791 Lmna lamin A gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0003159 abnormal esophageal smooth muscle morphology IAGP N RGD:5509061 20150319 MGI PMID:12748643 732791 Lmna lamin A gene MP:0003159 abnormal esophageal smooth muscle morphology IAGP N RGD:5509061 20160407 MGI PMID:25652409 732791 Lmna lamin A gene MP:0003330 abnormal auditory tube morphology IAGP N RGD:5509061 20180222 MGI PMID:22819531 732791 Lmna lamin A gene MP:0003358 abnormal hypaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:10579712 732791 Lmna lamin A gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0003756 abnormal hard palate morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0003786 premature aging IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0003786 premature aging IAGP N RGD:5509061 20220721 MGI PMID:29703891 732791 Lmna lamin A gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0003840 abnormal coronal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0003841 abnormal lambdoid suture morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0003878 abnormal ear physiology IAGP N RGD:5509061 20180222 MGI PMID:22819531 732791 Lmna lamin A gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:15972724 732791 Lmna lamin A gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0003916 decreased heart left ventricle weight IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21088111 732791 Lmna lamin A gene MP:0003978 decreased circulating carnitine level IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:21464947 732791 Lmna lamin A gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:21464947 732791 Lmna lamin A gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0004142 abnormal muscle tone IAGP N RGD:5509061 20220421 MGI PMID:22331516 732791 Lmna lamin A gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0004548 dilated esophagus IAGP N RGD:5509061 20160407 MGI PMID:25652409 732791 Lmna lamin A gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:15972724 732791 Lmna lamin A gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0004675 rib fractures IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0004675 rib fractures IAGP N RGD:5509061 20141003 MGI PMID:18757838 732791 Lmna lamin A gene MP:0004675 rib fractures IAGP N RGD:5509061 20141003 MGI PMID:18769635 732791 Lmna lamin A gene MP:0004675 rib fractures IAGP N RGD:5509061 20141003 MGI PMID:21088111 732791 Lmna lamin A gene MP:0004680 small xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20180222 MGI PMID:22819531 732791 Lmna lamin A gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170824 MGI PMID:22773734 732791 Lmna lamin A gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170907 MGI PMID:26436652 732791 Lmna lamin A gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:14996939 732791 Lmna lamin A gene MP:0005159 azoospermia IAGP N RGD:5509061 20151126 MGI PMID:23382700 732791 Lmna lamin A gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20151126 MGI PMID:23382700 732791 Lmna lamin A gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 732791 Lmna lamin A gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11855819 732791 Lmna lamin A gene MP:0005331 insulin resistance IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15972724 732791 Lmna lamin A gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20220721 MGI PMID:29703891 732791 Lmna lamin A gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:11799477 732791 Lmna lamin A gene MP:0005426 tachypnea IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18769635 732791 Lmna lamin A gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11855819 732791 Lmna lamin A gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141030 MGI PMID:23690466 732791 Lmna lamin A gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21088111 732791 Lmna lamin A gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15972724 732791 Lmna lamin A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0006018 abnormal tympanic membrane morphology IAGP N RGD:5509061 20180222 MGI PMID:22819531 732791 Lmna lamin A gene MP:0006057 decreased vascular endothelial cell number IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0006213 shallow orbits IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0006325 impaired hearing IAGP N RGD:5509061 20180222 MGI PMID:22819531 732791 Lmna lamin A gene MP:0008012 duodenum polyps IAGP N RGD:5509061 20160616 MGI PMID:25578479 732791 Lmna lamin A gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20141003 MGI PMID:21464947 732791 Lmna lamin A gene MP:0008244 abnormal peritoneal macrophage morphology IAGP N RGD:5509061 20180222 MGI PMID:22819531 732791 Lmna lamin A gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20240523 MGI 732791 Lmna lamin A gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:14996939 732791 Lmna lamin A gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20151126 MGI PMID:23382700 732791 Lmna lamin A gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0008526 decreased cranium width IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:20421363 732791 Lmna lamin A gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18769635 732791 Lmna lamin A gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20220721 MGI PMID:29703891 732791 Lmna lamin A gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18769635 732791 Lmna lamin A gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0008890 abnormal nuclear lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0008890 abnormal nuclear lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:21464947 732791 Lmna lamin A gene MP:0008890 abnormal nuclear lamina morphology IAGP N RGD:5509061 20180222 MGI PMID:22819531 732791 Lmna lamin A gene MP:0009105 penis prolapse IAGP N RGD:5509061 20220721 MGI PMID:29703891 732791 Lmna lamin A gene MP:0009247 meteorism IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:23998933 732791 Lmna lamin A gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20160616 MGI PMID:25578479 732791 Lmna lamin A gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20160616 MGI PMID:25578479 732791 Lmna lamin A gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0009416 cardiac muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:12748643 732791 Lmna lamin A gene MP:0009416 cardiac muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:15972724 732791 Lmna lamin A gene MP:0009416 cardiac muscle degeneration IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20151126 MGI PMID:23382700 732791 Lmna lamin A gene MP:0009480 distended cecum IAGP N RGD:5509061 20160407 MGI PMID:25652409 732791 Lmna lamin A gene MP:0009536 abnormal interstitial cell of Cajal morphology IAGP N RGD:5509061 20160407 MGI PMID:25652409 732791 Lmna lamin A gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141030 MGI PMID:23690466 732791 Lmna lamin A gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0009762 abnormal mitotic spindle assembly checkpoint IAGP N RGD:5509061 20141003 MGI PMID:21464947 732791 Lmna lamin A gene MP:0009825 cornea ulcer IEA N RGD:5509061 20201231 MGI 732791 Lmna lamin A gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20161117 MGI PMID:26999604 732791 Lmna lamin A gene MP:0009871 abnormal aorta tunica adventitia morphology IAGP N RGD:5509061 20161117 MGI PMID:26999604 732791 Lmna lamin A gene MP:0009871 abnormal aorta tunica adventitia morphology IAGP N RGD:5509061 20220721 MGI PMID:29703891 732791 Lmna lamin A gene MP:0009878 decreased susceptibility to bone fracture IAGP N RGD:5509061 20141003 MGI PMID:20439468 732791 Lmna lamin A gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16862216 732791 Lmna lamin A gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21088111 732791 Lmna lamin A gene MP:0010031 abnormal cranium size IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0010043 abnormal frontonasal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:10579712 732791 Lmna lamin A gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0010520 sinoatrial block IAGP N RGD:5509061 20141003 MGI PMID:15548545 732791 Lmna lamin A gene MP:0010522 calcified aorta IAGP N RGD:5509061 20141030 MGI PMID:23690466 732791 Lmna lamin A gene MP:0010523 calcified thoracic aorta IAGP N RGD:5509061 20141030 MGI PMID:23690466 732791 Lmna lamin A gene MP:0010524 calcified aortic arch IAGP N RGD:5509061 20141030 MGI PMID:23690466 732791 Lmna lamin A gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:22030750 732791 Lmna lamin A gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20151126 MGI PMID:23382700 732791 Lmna lamin A gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22090424 732791 Lmna lamin A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23998933 732791 Lmna lamin A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160616 MGI PMID:25578479 732791 Lmna lamin A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732791 Lmna lamin A gene MP:0011168 abnormal fat cell differentiation IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0011570 esophageal achalasia IAGP N RGD:5509061 20160407 MGI PMID:25652409 732791 Lmna lamin A gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:21464947 732791 Lmna lamin A gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20170824 MGI PMID:23575224 732791 Lmna lamin A gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20180222 MGI PMID:22819531 732791 Lmna lamin A gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0012107 enhanced exercise endurance IAGP N RGD:5509061 20220421 MGI PMID:22331516 732791 Lmna lamin A gene MP:0013192 decreased sebaceous gland number IAGP N RGD:5509061 20141127 MGI PMID:12748643 732791 Lmna lamin A gene MP:0013193 sebaceous gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20376364 732791 Lmna lamin A gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20151112 MGI PMID:21818413 732791 Lmna lamin A gene MP:0013458 decreased eccrine gland number IAGP N RGD:5509061 20150319 MGI PMID:12748643 732791 Lmna lamin A gene MP:0013466 keratoconjunctivitis sicca IAGP N RGD:5509061 20220721 MGI PMID:29703891 732791 Lmna lamin A gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0014170 increased brown adipose tissue mass IAGP N RGD:5509061 20230831 MGI PMID:36583724 732791 Lmna lamin A gene MP:0014516 abnormal middle ear development IAGP N RGD:5509061 20240822 MGI PMID:22819531 732791 Lmna lamin A gene MP:0020084 short ears IAGP N RGD:5509061 20170914 MGI PMID:20376364 732791 Lmna lamin A gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:20376364 732791 Lmna lamin A gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:16862216 732791 Lmna lamin A gene MP:0020324 jejunum polyps IAGP N RGD:5509061 20160714 MGI PMID:25578479 732791 Lmna lamin A gene MP:0020329 decreased capillary density IAGP N RGD:5509061 20200604 MGI PMID:32128409 732791 Lmna lamin A gene MP:0020900 abnormal middle ear epithelium morphology IAGP N RGD:5509061 20191219 MGI PMID:22819531 732791 Lmna lamin A gene MP:0020903 increased middle ear goblet cell number IAGP N RGD:5509061 20191219 MGI PMID:22819531 732791 Lmna lamin A gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:16862216 732791 Lmna lamin A gene MP:0030080 small lower incisors IAGP N RGD:5509061 20170928 MGI PMID:22030750 732791 Lmna lamin A gene MP:0030090 short upper incisors IAGP N RGD:5509061 20170928 MGI PMID:20376364 732791 Lmna lamin A gene MP:0030160 abnormal auditory bulla morphology IAGP N RGD:5509061 20180222 MGI PMID:22819531 732791 Lmna lamin A gene MP:0030413 tympanic membrane retraction IAGP N RGD:5509061 20180222 MGI PMID:22819531 732791 Lmna lamin A gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:22030750 732791 Lmna lamin A gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:22030750 732791 Lmna lamin A gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15548545 732791 Lmna lamin A gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15972724 732791 Lmna lamin A gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:20421363 732791 Lmna lamin A gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:32128409 732797 Gdf10 growth differentiation factor 10 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 732797 Gdf10 growth differentiation factor 10 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 732797 Gdf10 growth differentiation factor 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10419686 732797 Gdf10 growth differentiation factor 10 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 732797 Gdf10 growth differentiation factor 10 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20221215 MGI 732799 Phkg2 phosphorylase kinase, gamma 2 (testis) gene MP:0002608 increased hematocrit IEA N RGD:5509061 20220519 MGI 732799 Phkg2 phosphorylase kinase, gamma 2 (testis) gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 732799 Phkg2 phosphorylase kinase, gamma 2 (testis) gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 732799 Phkg2 phosphorylase kinase, gamma 2 (testis) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 732802 Ide insulin degrading enzyme gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20160804 MGI 732802 Ide insulin degrading enzyme gene MP:0000455 abnormal maxilla morphology IEA N RGD:5509061 20160804 MGI 732802 Ide insulin degrading enzyme gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20191128 MGI PMID:30807788 732802 Ide insulin degrading enzyme gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 732802 Ide insulin degrading enzyme gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12634421 732802 Ide insulin degrading enzyme gene MP:0002074 abnormal hair texture IEA N RGD:5509061 20160804 MGI 732802 Ide insulin degrading enzyme gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12634421 732802 Ide insulin degrading enzyme gene MP:0002833 increased heart weight IEA N RGD:5509061 20160804 MGI 732802 Ide insulin degrading enzyme gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 732802 Ide insulin degrading enzyme gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:12634421 732802 Ide insulin degrading enzyme gene MP:0003674 oxidative stress IAGP N RGD:5509061 20191128 MGI PMID:30807788 732802 Ide insulin degrading enzyme gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20191128 MGI PMID:30807788 732802 Ide insulin degrading enzyme gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 732802 Ide insulin degrading enzyme gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12634421 732802 Ide insulin degrading enzyme gene MP:0005358 abnormal incisor morphology IEA N RGD:5509061 20160804 MGI 732802 Ide insulin degrading enzyme gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20191128 MGI PMID:30807788 732802 Ide insulin degrading enzyme gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 732802 Ide insulin degrading enzyme gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20160804 MGI 732802 Ide insulin degrading enzyme gene MP:0009325 necrospermia IAGP N RGD:5509061 20220303 MGI PMID:30807788 732802 Ide insulin degrading enzyme gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160804 MGI 732802 Ide insulin degrading enzyme gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20191128 MGI PMID:30807788 732802 Ide insulin degrading enzyme gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20191128 MGI PMID:30807788 732808 Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:21075145 732808 Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide gene MP:0000836 abnormal substantia nigra morphology IAGP N RGD:5509061 20141003 MGI PMID:21075145 732808 Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21075145 732808 Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11836246 732808 Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:21075145 732808 Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:21075145 732808 Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:21075145 732808 Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide gene MP:0005443 abnormal ethanol metabolism IAGP N RGD:5509061 20141003 MGI PMID:10358022 732808 Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide gene MP:0005443 abnormal ethanol metabolism IAGP N RGD:5509061 20141003 MGI PMID:10402668 732808 Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide gene MP:0005444 abnormal retinol metabolism IAGP N RGD:5509061 20141003 MGI PMID:10402668 732808 Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide gene MP:0005444 abnormal retinol metabolism IAGP N RGD:5509061 20141003 MGI PMID:11836246 732808 Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:21075145 732808 Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21075145 732808 Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11836246 732808 Adh7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide gene MP:0011232 abnormal vitamin A level IAGP N RGD:5509061 20141003 MGI PMID:10358022 732814 Casc3 exon junction complex subunit gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20241107 MGI 732814 Casc3 exon junction complex subunit gene MP:0000274 enlarged heart IEA N RGD:5509061 20241107 MGI 732814 Casc3 exon junction complex subunit gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20241017 MGI 732814 Casc3 exon junction complex subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170511 MGI PMID:27780844 732814 Casc3 exon junction complex subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:27780844 732814 Casc3 exon junction complex subunit gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20241107 MGI 732814 Casc3 exon junction complex subunit gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20170511 MGI PMID:27780844 732814 Casc3 exon junction complex subunit gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20170511 MGI PMID:27780844 732814 Casc3 exon junction complex subunit gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20170511 MGI PMID:27780844 732814 Casc3 exon junction complex subunit gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20241107 MGI 732814 Casc3 exon junction complex subunit gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20241107 MGI 732814 Casc3 exon junction complex subunit gene MP:0009331 absent primitive node IEA N RGD:5509061 20241017 MGI 732814 Casc3 exon junction complex subunit gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 732814 Casc3 exon junction complex subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170511 MGI PMID:27780844 732814 Casc3 exon junction complex subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20241107 MGI 732814 Casc3 exon junction complex subunit gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20241107 MGI 732814 Casc3 exon junction complex subunit gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20241017 MGI PMID:27780844 732814 Casc3 exon junction complex subunit gene MP:0012531 delayed limb development IAGP N RGD:5509061 20170511 MGI PMID:27780844 732814 Casc3 exon junction complex subunit gene MP:0012724 absent head fold IEA N RGD:5509061 20241017 MGI 732814 Casc3 exon junction complex subunit gene MP:0014134 abnormal embryo morphology IAGP N RGD:5509061 20170511 MGI PMID:27780844 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:24009395 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:10369265 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000033 absent scala media IAGP N RGD:5509061 20141003 MGI PMID:11377879 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20160929 MGI PMID:27534441 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10401008 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:11377879 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:10369265 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:11377879 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000046 abnormal sulcus ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:10401008 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:10401008 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20201022 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20201022 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000500 small intestinal prolapse IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000510 remittent intestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20201022 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:10831596 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:10369265 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10369265 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:24009395 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:9799839 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001396 unidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10369265 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:24009395 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:10369265 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:9799839 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001411 spinning IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:10369265 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:24009395 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20201022 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10369265 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:10369265 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:24009395 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:9799839 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0001967 deafness IAGP N RGD:5509061 20160929 MGI PMID:27534441 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20201022 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:10401008 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20201022 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:10401008 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11377879 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0003151 absent tunnel of Corti IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0003151 absent tunnel of Corti IAGP N RGD:5509061 20141003 MGI PMID:11377879 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0003169 abnormal scala media morphology IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20201022 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0003878 abnormal ear physiology IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:24009395 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004294 abnormal type II spiral ligament fibrocytes IAGP N RGD:5509061 20141003 MGI PMID:11377879 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004296 abnormal type IV spiral ligament fibrocytes IAGP N RGD:5509061 20141003 MGI PMID:11377879 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004300 abnormal organ of Corti supporting cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10401008 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004300 abnormal organ of Corti supporting cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11377879 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004301 absent organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:10369265 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004329 vestibular saccular degeneration IAGP N RGD:5509061 20141003 MGI PMID:24009395 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004332 utricular degeneration IAGP N RGD:5509061 20141003 MGI PMID:24009395 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004366 abnormal strial marginal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004366 abnormal strial marginal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11377879 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11377879 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:10369265 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:10401008 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004482 abnormal interdental cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10401008 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004482 abnormal interdental cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11377879 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20201022 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:24009395 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20201022 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0006021 abnormal Reissner membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11377879 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:10369265 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:10401008 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:11377879 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:24009395 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:18833191 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0006331 abnormal patterning of the organ of Corti IAGP N RGD:5509061 20141003 MGI PMID:11377879 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:10369265 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:10683373 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0009478 coiled cecum IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20201022 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10480906 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20201022 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0011739 abnormal Boettcher cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11377879 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18833191 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:9799839 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0013799 abnormal intestinal goblet cell physiology IAGP N RGD:5509061 20201022 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0014030 abnormal mucous gland physiology IAGP N RGD:5509061 20201022 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0014219 decreased intestinal mucosa thickness IAGP N RGD:5509061 20201022 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0014222 decreased colon goblet cell number IAGP N RGD:5509061 20201022 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0014484 decreased feces water content IAGP N RGD:5509061 20240704 MGI PMID:31655271 732817 Slc12a2 solute carrier family 12, member 2 gene MP:0020848 abnormal exocytosis IAGP N RGD:5509061 20201022 MGI PMID:31655271 732820 Ptgr1 prostaglandin reductase 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 732820 Ptgr1 prostaglandin reductase 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 732820 Ptgr1 prostaglandin reductase 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20201022 MGI 732822 Daxx Fas death domain-associated protein gene MP:0000274 enlarged heart IEA N RGD:5509061 20200402 MGI 732822 Daxx Fas death domain-associated protein gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:10444590 732822 Daxx Fas death domain-associated protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10444590 732822 Daxx Fas death domain-associated protein gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10444590 732822 Daxx Fas death domain-associated protein gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 732822 Daxx Fas death domain-associated protein gene MP:0003708 binucleate IAGP N RGD:5509061 20141003 MGI PMID:15252119 732822 Daxx Fas death domain-associated protein gene MP:0003891 increased allantois apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10444590 732822 Daxx Fas death domain-associated protein gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15252119 732822 Daxx Fas death domain-associated protein gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:10444590 732822 Daxx Fas death domain-associated protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10444590 732822 Daxx Fas death domain-associated protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15252119 732822 Daxx Fas death domain-associated protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732822 Daxx Fas death domain-associated protein gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10444590 732822 Daxx Fas death domain-associated protein gene MP:0013181 absent placenta IAGP N RGD:5509061 20141003 MGI PMID:10444590 732822 Daxx Fas death domain-associated protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 732822 Daxx Fas death domain-associated protein gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150219 MGI PMID:10444590 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0003608 prostate gland inflammation IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0009646 urinary bladder inflammation IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0012712 spinal cord degeneration IAGP N RGD:5509061 20150924 MGI PMID:24828632 732826 Slc33a1 solute carrier family 33 (acetyl-CoA transporter), member 1 gene MP:0013905 preputial gland inflammation IAGP N RGD:5509061 20150924 MGI PMID:24828632 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12577054 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12900523 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:14702109 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:11801676 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:14702109 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:12209637 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:12577054 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11801676 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16174101 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:12577054 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:12577054 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11801676 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12577054 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:12577054 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12577054 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:12577054 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12209637 732827 Tnfsf10 tumor necrosis factor (ligand) superfamily, member 10 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:14702109 732831 Akap4 A kinase anchor protein 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20240822 MGI PMID:38050179 732831 Akap4 A kinase anchor protein 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12167408 732831 Akap4 A kinase anchor protein 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20220224 MGI PMID:31969357 732831 Akap4 A kinase anchor protein 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20240822 MGI PMID:38050179 732831 Akap4 A kinase anchor protein 4 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:12167408 732831 Akap4 A kinase anchor protein 4 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12167408 732831 Akap4 A kinase anchor protein 4 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220224 MGI PMID:31969357 732831 Akap4 A kinase anchor protein 4 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20240822 MGI PMID:38050179 732831 Akap4 A kinase anchor protein 4 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:12167408 732831 Akap4 A kinase anchor protein 4 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20220224 MGI PMID:31969357 732831 Akap4 A kinase anchor protein 4 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:12167408 732831 Akap4 A kinase anchor protein 4 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20220224 MGI PMID:31969357 732831 Akap4 A kinase anchor protein 4 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20240822 MGI PMID:38050179 732831 Akap4 A kinase anchor protein 4 gene MP:0009280 decreased activated sperm motility IAGP N RGD:5509061 20141003 MGI PMID:12167408 732831 Akap4 A kinase anchor protein 4 gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20141003 MGI PMID:12167408 732831 Akap4 A kinase anchor protein 4 gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20220224 MGI PMID:31969357 732831 Akap4 A kinase anchor protein 4 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:12167408 732831 Akap4 A kinase anchor protein 4 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20141003 MGI PMID:12167408 732831 Akap4 A kinase anchor protein 4 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20220224 MGI PMID:31969357 732831 Akap4 A kinase anchor protein 4 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20240822 MGI PMID:38050179 732831 Akap4 A kinase anchor protein 4 gene MP:0009837 abnormal sperm end piece morphology IAGP N RGD:5509061 20141003 MGI PMID:12167408 732831 Akap4 A kinase anchor protein 4 gene MP:0014464 decreased sperm mitochondrial sheath size IAGP N RGD:5509061 20240613 MGI PMID:12167408 732831 Akap4 A kinase anchor protein 4 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20240822 MGI PMID:38050179 732831 Akap4 A kinase anchor protein 4 gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20240822 MGI PMID:38050179 732832 C9 complement component 9 gene MP:0002473 impaired complement classical pathway IAGP N RGD:5509061 20210415 MGI PMID:27444648 732832 C9 complement component 9 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 732832 C9 complement component 9 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160421 MGI 732832 C9 complement component 9 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20210415 MGI PMID:27444648 732832 C9 complement component 9 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20210415 MGI PMID:27444648 732834 Eif4e eukaryotic translation initiation factor 4E gene MP:0001262 decreased body weight IAGP N RGD:5509061 20241031 MGI PMID:34013332 732834 Eif4e eukaryotic translation initiation factor 4E gene MP:0001727 abnormal embryo implantation IAGP N RGD:5509061 20241031 MGI PMID:34013332 732834 Eif4e eukaryotic translation initiation factor 4E gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20679199 732834 Eif4e eukaryotic translation initiation factor 4E gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20160304 MGI PMID:26095252 732834 Eif4e eukaryotic translation initiation factor 4E gene MP:0003674 oxidative stress IAGP N RGD:5509061 20160304 MGI PMID:26095252 732834 Eif4e eukaryotic translation initiation factor 4E gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20241031 MGI PMID:34013332 732834 Eif4e eukaryotic translation initiation factor 4E gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20679199 732834 Eif4e eukaryotic translation initiation factor 4E gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20160304 MGI PMID:26095252 732834 Eif4e eukaryotic translation initiation factor 4E gene MP:0010267 decreased lung tumor incidence IAGP N RGD:5509061 20160304 MGI PMID:26095252 732834 Eif4e eukaryotic translation initiation factor 4E gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20241031 MGI PMID:34013332 732834 Eif4e eukaryotic translation initiation factor 4E gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20200514 MGI 732834 Eif4e eukaryotic translation initiation factor 4E gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20241031 MGI PMID:34013332 732834 Eif4e eukaryotic translation initiation factor 4E gene MP:0013272 abnormal translation IAGP N RGD:5509061 20241031 MGI PMID:34013332 732835 Dock9 dedicator of cytokinesis 9 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210520 MGI 732835 Dock9 dedicator of cytokinesis 9 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 732835 Dock9 dedicator of cytokinesis 9 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 732835 Dock9 dedicator of cytokinesis 9 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240523 MGI 732835 Dock9 dedicator of cytokinesis 9 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20220811 MGI 732835 Dock9 dedicator of cytokinesis 9 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 732835 Dock9 dedicator of cytokinesis 9 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 732835 Dock9 dedicator of cytokinesis 9 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 732835 Dock9 dedicator of cytokinesis 9 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20181227 MGI 732839 Grp gastrin releasing peptide gene MP:0000274 enlarged heart IEA N RGD:5509061 20200402 MGI 732839 Grp gastrin releasing peptide gene MP:0001440 abnormal grooming behavior IAGP N RGD:5509061 20180201 MGI PMID:29133874 732839 Grp gastrin releasing peptide gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 732839 Grp gastrin releasing peptide gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 732841 Glra3 glycine receptor, alpha 3 subunit gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:15131310 732841 Glra3 glycine receptor, alpha 3 subunit gene MP:0002906 increased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20111116 MGI 732841 Glra3 glycine receptor, alpha 3 subunit gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17920294 732841 Glra3 glycine receptor, alpha 3 subunit gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:17920294 732848 Scnn1g sodium channel, nonvoltage-gated 1 gamma gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:9788978 732848 Scnn1g sodium channel, nonvoltage-gated 1 gamma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19036848 732848 Scnn1g sodium channel, nonvoltage-gated 1 gamma gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:9788978 732848 Scnn1g sodium channel, nonvoltage-gated 1 gamma gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:9788978 732848 Scnn1g sodium channel, nonvoltage-gated 1 gamma gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:9788978 732848 Scnn1g sodium channel, nonvoltage-gated 1 gamma gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:9788978 732848 Scnn1g sodium channel, nonvoltage-gated 1 gamma gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:9788978 732848 Scnn1g sodium channel, nonvoltage-gated 1 gamma gene MP:0005634 decreased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:9788978 732848 Scnn1g sodium channel, nonvoltage-gated 1 gamma gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:9788978 732848 Scnn1g sodium channel, nonvoltage-gated 1 gamma gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9788978 732848 Scnn1g sodium channel, nonvoltage-gated 1 gamma gene MP:0011163 increased wet-to-dry lung weight ratio IAGP N RGD:5509061 20141003 MGI PMID:9788978 732848 Scnn1g sodium channel, nonvoltage-gated 1 gamma gene MP:0011462 increased urine bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:9788978 732848 Scnn1g sodium channel, nonvoltage-gated 1 gamma gene MP:0014182 decreased respiratory epithelial sodium ion transmembrane transport IAGP N RGD:5509061 20160526 MGI PMID:9788978 732848 Scnn1g sodium channel, nonvoltage-gated 1 gamma gene MP:0014206 decreased intestinal epithelial sodium ion transmembrane transport IAGP N RGD:5509061 20160526 MGI PMID:9788978 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20210520 MGI 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20210520 MGI 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0000653 abnormal sex gland morphology IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20210520 MGI 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20210520 MGI 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0002494 increased IgM level IEA N RGD:5509061 20190418 MGI 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9002646 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0004827 increased susceptibility to autoimmune hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0004827 increased susceptibility to autoimmune hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:9002646 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0005002 abnormal T cell clonal deletion IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0008037 abnormal T cell morphology IEA N RGD:5509061 20190418 MGI 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20190418 MGI 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19084435 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0008047 absent uterine NK cells IAGP N RGD:5509061 20141003 MGI PMID:9002646 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190110 MGI 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20190418 MGI 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0008180 abnormal marginal zone B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12196288 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0008247 abnormal mononuclear cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:7770771 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0009097 absent endometrial glands IAGP N RGD:5509061 20141003 MGI PMID:9002646 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190110 MGI 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0010848 decreased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190110 MGI 732849 Il2rb interleukin 2 receptor, beta chain gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20190110 MGI 732851 Hoxa1 homeobox A1 gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:10529419 732851 Hoxa1 homeobox A1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0000033 absent scala media IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0000039 abnormal otic capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0000040 absent middle ear ossicles IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0000041 absent endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0000041 absent endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10529419 732851 Hoxa1 homeobox A1 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0000080 abnormal exoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10529419 732851 Hoxa1 homeobox A1 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:16890163 732851 Hoxa1 homeobox A1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:10529419 732851 Hoxa1 homeobox A1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0000842 absent superior olivary complex IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0000843 absent facial nuclei IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0000843 absent facial nuclei IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0000910 small facial motor nucleus IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0000910 small facial motor nucleus IAGP N RGD:5509061 20141003 MGI PMID:16890163 732851 Hoxa1 homeobox A1 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20190228 MGI PMID:8102800 732851 Hoxa1 homeobox A1 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16890163 732851 Hoxa1 homeobox A1 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20190228 MGI PMID:8102800 732851 Hoxa1 homeobox A1 gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0001098 small superior glossopharyngeal ganglion IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0001101 abnormal superior vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0001102 small superior vagus ganglion IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:10529419 732851 Hoxa1 homeobox A1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10529419 732851 Hoxa1 homeobox A1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:16890163 732851 Hoxa1 homeobox A1 gene MP:0001993 abnormal blinking IAGP N RGD:5509061 20171005 MGI PMID:16890163 732851 Hoxa1 homeobox A1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0002163 abnormal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10529419 732851 Hoxa1 homeobox A1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16890163 732851 Hoxa1 homeobox A1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20171203 732851 Hoxa1 homeobox A1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9053316 732851 Hoxa1 homeobox A1 gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0002316 anoxia IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:11532923 732851 Hoxa1 homeobox A1 gene MP:0003146 absent cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0003146 absent cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0003147 absent cochlea IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0003147 absent cochlea IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0003165 absent superior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0003494 parathyroid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:10529419 732851 Hoxa1 homeobox A1 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0004315 absent vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0004330 abnormal vestibular saccular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0004369 absent utricle IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0004561 absent facial nerve IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0004568 fusion of glossopharyngeal and vagus nerve IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0004715 absent vestibulocochlear nerve IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0004715 absent vestibulocochlear nerve IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0004717 absent cochlear nerve IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0004719 absent vestibular nerve IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0004923 absent common crus IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10529419 732851 Hoxa1 homeobox A1 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20141003 MGI PMID:10529419 732851 Hoxa1 homeobox A1 gene MP:0006013 absent endolymphatic sac IAGP N RGD:5509061 20141003 MGI PMID:11528388 732851 Hoxa1 homeobox A1 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:21784065 732851 Hoxa1 homeobox A1 gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20141003 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0008372 small malleus IAGP N RGD:5509061 20141003 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0008372 small malleus IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0009806 abnormal otic vesicle morphology IAGP N RGD:5509061 20190228 MGI PMID:8102800 732851 Hoxa1 homeobox A1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:10529419 732851 Hoxa1 homeobox A1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10529419 732851 Hoxa1 homeobox A1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21784065 732851 Hoxa1 homeobox A1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1680563 732851 Hoxa1 homeobox A1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1346922 732851 Hoxa1 homeobox A1 gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0012730 abnormal internal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0012731 abnormal external carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21940751 732851 Hoxa1 homeobox A1 gene MP:0012746 abnormal neural crest cell delamination IAGP N RGD:5509061 20141003 MGI PMID:11532923 732851 Hoxa1 homeobox A1 gene MP:0012757 abnormal cranial neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0012794 increased rhombomere 3 size IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0012797 decreased rhombomere 4 size IAGP N RGD:5509061 20190228 MGI PMID:8102800 732851 Hoxa1 homeobox A1 gene MP:0012799 absent rhombomere 4 IAGP N RGD:5509061 20141003 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0012801 decreased rhombomere 5 size IAGP N RGD:5509061 20190228 MGI PMID:8102800 732851 Hoxa1 homeobox A1 gene MP:0012803 absent rhombomere 5 IAGP N RGD:5509061 20141003 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0012816 abnormal rhombomere boundary morphology IAGP N RGD:5509061 20190228 MGI PMID:8102800 732851 Hoxa1 homeobox A1 gene MP:0012817 rhombomere fusion IAGP N RGD:5509061 20141003 MGI PMID:15367676 732851 Hoxa1 homeobox A1 gene MP:0013224 absent second pharyngeal pouch IAGP N RGD:5509061 20150101 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0013225 abnormal third pharyngeal pouch morphology IAGP N RGD:5509061 20150101 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0030040 absent facial muscle IAGP N RGD:5509061 20170921 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0030106 small incus IAGP N RGD:5509061 20171005 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0030123 small middle ear ossicles IAGP N RGD:5509061 20171005 MGI PMID:10529419 732851 Hoxa1 homeobox A1 gene MP:0030141 facial paralysis IAGP N RGD:5509061 20171005 MGI PMID:16890163 732851 Hoxa1 homeobox A1 gene MP:0030146 abnormal digastric posterior belly morphology IAGP N RGD:5509061 20171005 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0030149 abnormal stylohyoid muscle morphology IAGP N RGD:5509061 20171005 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0030174 absent orbicularis oculi muscle IAGP N RGD:5509061 20171005 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0030177 absent levator labii superioris muscle IAGP N RGD:5509061 20171005 MGI PMID:10529420 732851 Hoxa1 homeobox A1 gene MP:0030207 absent zygomaticus muscle IAGP N RGD:5509061 20171019 MGI PMID:10529420 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:17194745 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18322240 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22862945 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18322240 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22862945 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22862945 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22862945 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:16054053 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:18322240 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:18322240 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:22862945 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:18039927 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18322240 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18039927 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22862945 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:18322240 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16054053 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16054053 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17194745 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17992262 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20141003 MGI PMID:17992262 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0003193 decreased cholesterol efflux IAGP N RGD:5509061 20141003 MGI PMID:18039927 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22862945 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:16054053 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20141003 MGI PMID:16054053 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:18322240 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22862945 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:17194745 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18322240 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18322240 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18039927 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17194745 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16054053 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:17194745 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17194745 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22862945 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18322240 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18322240 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0008112 abnormal monocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:18322240 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:18322240 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18322240 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0008570 lipidosis IAGP N RGD:5509061 20141003 MGI PMID:18322240 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:22862945 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0008690 increased interleukin-23 secretion IAGP N RGD:5509061 20141003 MGI PMID:22862945 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17992262 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17194745 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20240704 MGI PMID:16054053 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:16054053 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:17194745 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:17194745 732854 Abcg1 ATP binding cassette subfamily G member 1 gene MP:0031632 increased lung cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:16054053 732856 Ilk integrin linked kinase gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:12671688 732856 Ilk integrin linked kinase gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12671688 732856 Ilk integrin linked kinase gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20170907 MGI PMID:16951252 732856 Ilk integrin linked kinase gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170907 MGI PMID:16951252 732856 Ilk integrin linked kinase gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12671688 732856 Ilk integrin linked kinase gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12671688 732856 Ilk integrin linked kinase gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 732856 Ilk integrin linked kinase gene MP:0001399 hyperactivity IEA N RGD:5509061 20170105 MGI 732856 Ilk integrin linked kinase gene MP:0001438 aphagia IAGP N RGD:5509061 20151217 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:20564195 732856 Ilk integrin linked kinase gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220519 MGI 732856 Ilk integrin linked kinase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20170105 MGI 732856 Ilk integrin linked kinase gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:23658024 732856 Ilk integrin linked kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0002083 premature death IAGP N RGD:5509061 20170907 MGI PMID:16951252 732856 Ilk integrin linked kinase gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:12835312 732856 Ilk integrin linked kinase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:12671688 732856 Ilk integrin linked kinase gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:12835312 732856 Ilk integrin linked kinase gene MP:0002574 increased vertical activity IEA N RGD:5509061 20201022 MGI 732856 Ilk integrin linked kinase gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:12835312 732856 Ilk integrin linked kinase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20170907 MGI PMID:16951252 732856 Ilk integrin linked kinase gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170907 MGI PMID:16951252 732856 Ilk integrin linked kinase gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:21593206 732856 Ilk integrin linked kinase gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:12671688 732856 Ilk integrin linked kinase gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:12671688 732856 Ilk integrin linked kinase gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0003624 anuria IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:21593206 732856 Ilk integrin linked kinase gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:12670870 732856 Ilk integrin linked kinase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23658024 732856 Ilk integrin linked kinase gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20141003 MGI PMID:12671688 732856 Ilk integrin linked kinase gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:23658024 732856 Ilk integrin linked kinase gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:12671688 732856 Ilk integrin linked kinase gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12670870 732856 Ilk integrin linked kinase gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:20564195 732856 Ilk integrin linked kinase gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:21593206 732856 Ilk integrin linked kinase gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170907 MGI PMID:16951252 732856 Ilk integrin linked kinase gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20170907 MGI PMID:16951252 732856 Ilk integrin linked kinase gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20170907 MGI PMID:16951252 732856 Ilk integrin linked kinase gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:12671688 732856 Ilk integrin linked kinase gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:12671688 732856 Ilk integrin linked kinase gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:20564195 732856 Ilk integrin linked kinase gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:20564195 732856 Ilk integrin linked kinase gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12671688 732856 Ilk integrin linked kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12670870 732856 Ilk integrin linked kinase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23658024 732856 Ilk integrin linked kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732856 Ilk integrin linked kinase gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23658024 732856 Ilk integrin linked kinase gene MP:0011194 abnormal hair follicle physiology IAGP N RGD:5509061 20141003 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0011282 increased podocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0011483 renal glomerular synechia IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0011846 decreased kidney collecting duct number IAGP N RGD:5509061 20141003 MGI PMID:19829382 732856 Ilk integrin linked kinase gene MP:0011856 abnormal glomerular filtration barrier function IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0011868 podocyte microvillus transformation IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0011868 podocyte microvillus transformation IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0011869 detached podocyte IAGP N RGD:5509061 20141003 MGI PMID:16611717 732856 Ilk integrin linked kinase gene MP:0011869 detached podocyte IAGP N RGD:5509061 20141003 MGI PMID:16837631 732856 Ilk integrin linked kinase gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20170907 MGI PMID:16951252 732856 Ilk integrin linked kinase gene MP:0012194 decreased keratinocyte migration IAGP N RGD:5509061 20141204 MGI PMID:18234842 732856 Ilk integrin linked kinase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 732857 Il12b interleukin 12b gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17082625 732857 Il12b interleukin 12b gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17082625 732857 Il12b interleukin 12b gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17351619 732857 Il12b interleukin 12b gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16688182 732857 Il12b interleukin 12b gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16688182 732857 Il12b interleukin 12b gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:12486099 732857 Il12b interleukin 12b gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17351619 732857 Il12b interleukin 12b gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16688182 732857 Il12b interleukin 12b gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16688182 732857 Il12b interleukin 12b gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:8766560 732857 Il12b interleukin 12b gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17389237 732857 Il12b interleukin 12b gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:9529155 732857 Il12b interleukin 12b gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20221110 MGI 732857 Il12b interleukin 12b gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8766560 732857 Il12b interleukin 12b gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:9529155 732857 Il12b interleukin 12b gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:17351619 732857 Il12b interleukin 12b gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:8766560 732857 Il12b interleukin 12b gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16778988 732857 Il12b interleukin 12b gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20141003 MGI PMID:17082625 732857 Il12b interleukin 12b gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9529155 732857 Il12b interleukin 12b gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:17351619 732857 Il12b interleukin 12b gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:16778988 732857 Il12b interleukin 12b gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:16688182 732857 Il12b interleukin 12b gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17082625 732857 Il12b interleukin 12b gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15240709 732857 Il12b interleukin 12b gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18264109 732857 Il12b interleukin 12b gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17351619 732857 Il12b interleukin 12b gene MP:0030466 alveolar process atrophy IAGP N RGD:5509061 20171221 MGI PMID:17305866 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18274553 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:17475776 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:17475776 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17475776 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19364479 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17475776 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:17475776 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18274553 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:19364479 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:19364479 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:17475776 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19364479 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18274553 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19364479 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17475776 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19364479 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0011191 increased embryonic epiblast cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17475776 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0011192 decreased embryonic epiblast cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17475776 732860 Tpt1 tumor protein, translationally-controlled 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:18274553 732862 Chek2 checkpoint kinase 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16357220 732862 Chek2 checkpoint kinase 2 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20190502 MGI PMID:30305635 732862 Chek2 checkpoint kinase 2 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15131084 732862 Chek2 checkpoint kinase 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20190502 MGI PMID:30305635 732862 Chek2 checkpoint kinase 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20210204 MGI PMID:33097538 732862 Chek2 checkpoint kinase 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20190502 MGI PMID:30305635 732862 Chek2 checkpoint kinase 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20190502 MGI PMID:30305635 732862 Chek2 checkpoint kinase 2 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15131084 732862 Chek2 checkpoint kinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16357220 732862 Chek2 checkpoint kinase 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20190502 MGI PMID:30305635 732862 Chek2 checkpoint kinase 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20190502 MGI PMID:30305635 732862 Chek2 checkpoint kinase 2 gene MP:0003010 decreased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12356735 732862 Chek2 checkpoint kinase 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:17174984 732862 Chek2 checkpoint kinase 2 gene MP:0003207 decreased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:12192050 732862 Chek2 checkpoint kinase 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16357220 732862 Chek2 checkpoint kinase 2 gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:17174984 732862 Chek2 checkpoint kinase 2 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:12192050 732862 Chek2 checkpoint kinase 2 gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12356735 732862 Chek2 checkpoint kinase 2 gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20150212 MGI PMID:12097646 732862 Chek2 checkpoint kinase 2 gene MP:0004244 abnormal miscarriage rate IAGP N RGD:5509061 20210204 MGI PMID:33097538 732862 Chek2 checkpoint kinase 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:12192050 732862 Chek2 checkpoint kinase 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20190502 MGI PMID:30305635 732862 Chek2 checkpoint kinase 2 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16357220 732862 Chek2 checkpoint kinase 2 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20210204 MGI PMID:33097538 732862 Chek2 checkpoint kinase 2 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20190502 MGI PMID:30305635 732862 Chek2 checkpoint kinase 2 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20210204 MGI PMID:33097538 732862 Chek2 checkpoint kinase 2 gene MP:0005432 abnormal pro-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16357220 732862 Chek2 checkpoint kinase 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17174984 732862 Chek2 checkpoint kinase 2 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20240523 MGI 732862 Chek2 checkpoint kinase 2 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20170209 MGI PMID:26158450 732862 Chek2 checkpoint kinase 2 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:15131084 732862 Chek2 checkpoint kinase 2 gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20210204 MGI PMID:33097538 732862 Chek2 checkpoint kinase 2 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20190502 MGI PMID:30305635 732862 Chek2 checkpoint kinase 2 gene MP:0010767 abnormal female meiosis I arrest IAGP N RGD:5509061 20210204 MGI PMID:33097538 732862 Chek2 checkpoint kinase 2 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20190502 MGI PMID:30305635 732862 Chek2 checkpoint kinase 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16357220 732863 Icos inducible T cell co-stimulator gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17549732 732863 Icos inducible T cell co-stimulator gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:12853164 732863 Icos inducible T cell co-stimulator gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11343123 732863 Icos inducible T cell co-stimulator gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:11343123 732863 Icos inducible T cell co-stimulator gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17549732 732863 Icos inducible T cell co-stimulator gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11343122 732863 Icos inducible T cell co-stimulator gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:17549732 732863 Icos inducible T cell co-stimulator gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:18292537 732863 Icos inducible T cell co-stimulator gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22700722 732863 Icos inducible T cell co-stimulator gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11343122 732863 Icos inducible T cell co-stimulator gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11343121 732863 Icos inducible T cell co-stimulator gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:11343122 732863 Icos inducible T cell co-stimulator gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:12853164 732863 Icos inducible T cell co-stimulator gene MP:0002391 abnormal Peyer's patch germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11343123 732863 Icos inducible T cell co-stimulator gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17549732 732863 Icos inducible T cell co-stimulator gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11343123 732863 Icos inducible T cell co-stimulator gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11343121 732863 Icos inducible T cell co-stimulator gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11343122 732863 Icos inducible T cell co-stimulator gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11343121 732863 Icos inducible T cell co-stimulator gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11343122 732863 Icos inducible T cell co-stimulator gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11343123 732863 Icos inducible T cell co-stimulator gene MP:0002764 short tibia IEA N RGD:5509061 20181227 MGI 732863 Icos inducible T cell co-stimulator gene MP:0002870 decreased anti-insulin autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:18292537 732863 Icos inducible T cell co-stimulator gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16200068 732863 Icos inducible T cell co-stimulator gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:18292537 732863 Icos inducible T cell co-stimulator gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:18292537 732863 Icos inducible T cell co-stimulator gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:11343121 732863 Icos inducible T cell co-stimulator gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:18292537 732863 Icos inducible T cell co-stimulator gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:11343123 732863 Icos inducible T cell co-stimulator gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0004942 abnormal B cell selection IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18292537 732863 Icos inducible T cell co-stimulator gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17549732 732863 Icos inducible T cell co-stimulator gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11343123 732863 Icos inducible T cell co-stimulator gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11343122 732863 Icos inducible T cell co-stimulator gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17549732 732863 Icos inducible T cell co-stimulator gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:11343121 732863 Icos inducible T cell co-stimulator gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0008093 abnormal memory B cell number IAGP N RGD:5509061 20141003 MGI PMID:17549732 732863 Icos inducible T cell co-stimulator gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:17549732 732863 Icos inducible T cell co-stimulator gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:17549732 732863 Icos inducible T cell co-stimulator gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12853164 732863 Icos inducible T cell co-stimulator gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:17549732 732863 Icos inducible T cell co-stimulator gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:11343123 732863 Icos inducible T cell co-stimulator gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:11343123 732863 Icos inducible T cell co-stimulator gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11343121 732863 Icos inducible T cell co-stimulator gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11343122 732863 Icos inducible T cell co-stimulator gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11343123 732863 Icos inducible T cell co-stimulator gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:11343122 732863 Icos inducible T cell co-stimulator gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:11343122 732863 Icos inducible T cell co-stimulator gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18292537 732863 Icos inducible T cell co-stimulator gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:17549732 732863 Icos inducible T cell co-stimulator gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:15629449 732863 Icos inducible T cell co-stimulator gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:15629449 732863 Icos inducible T cell co-stimulator gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:17549732 732863 Icos inducible T cell co-stimulator gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:17549732 732863 Icos inducible T cell co-stimulator gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:16200068 732863 Icos inducible T cell co-stimulator gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:11343121 732863 Icos inducible T cell co-stimulator gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:11343121 732863 Icos inducible T cell co-stimulator gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:11343122 732863 Icos inducible T cell co-stimulator gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0009058 decreased interleukin-21 secretion IAGP N RGD:5509061 20141003 MGI PMID:19915142 732863 Icos inducible T cell co-stimulator gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:18292537 732863 Icos inducible T cell co-stimulator gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22700722 732863 Icos inducible T cell co-stimulator gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15629449 732867 Spata6 spermatogenesis associated 6 gene MP:0001925 male infertility IAGP N RGD:5509061 20160310 MGI PMID:25605924 732867 Spata6 spermatogenesis associated 6 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20160310 MGI PMID:25605924 732867 Spata6 spermatogenesis associated 6 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20160310 MGI PMID:25605924 732867 Spata6 spermatogenesis associated 6 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20160310 MGI PMID:25605924 732867 Spata6 spermatogenesis associated 6 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20160310 MGI PMID:25605924 732867 Spata6 spermatogenesis associated 6 gene MP:0002764 short tibia IEA N RGD:5509061 20160114 MGI 732867 Spata6 spermatogenesis associated 6 gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 732867 Spata6 spermatogenesis associated 6 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20160310 MGI PMID:25605924 732867 Spata6 spermatogenesis associated 6 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20160310 MGI PMID:25605924 732867 Spata6 spermatogenesis associated 6 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20160310 MGI PMID:25605924 732867 Spata6 spermatogenesis associated 6 gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20160310 MGI PMID:25605924 732867 Spata6 spermatogenesis associated 6 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20160310 MGI PMID:25605924 732867 Spata6 spermatogenesis associated 6 gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20160310 MGI PMID:25605924 732867 Spata6 spermatogenesis associated 6 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20160310 MGI PMID:25605924 732867 Spata6 spermatogenesis associated 6 gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20160310 MGI PMID:25605924 732867 Spata6 spermatogenesis associated 6 gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20160310 MGI PMID:25605924 732867 Spata6 spermatogenesis associated 6 gene MP:0009837 abnormal sperm end piece morphology IAGP N RGD:5509061 20160310 MGI PMID:25605924 732867 Spata6 spermatogenesis associated 6 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20160310 MGI PMID:25605924 732869 Mcam melanoma cell adhesion molecule gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220519 MGI 732869 Mcam melanoma cell adhesion molecule gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 732869 Mcam melanoma cell adhesion molecule gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:23256918 732869 Mcam melanoma cell adhesion molecule gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:22718841 732869 Mcam melanoma cell adhesion molecule gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:23256918 732869 Mcam melanoma cell adhesion molecule gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220519 MGI 732869 Mcam melanoma cell adhesion molecule gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20141003 MGI PMID:23256918 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18820241 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18820241 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:12062084 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17289919 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18820241 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12062084 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17289919 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0002646 increased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:12062084 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17289919 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:12062084 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0003378 early sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:17289919 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:12062084 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:12062085 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:12062085 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17289919 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20141003 MGI PMID:17289919 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0004928 increased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:17289919 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18820241 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12062085 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18820241 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:12062084 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12062084 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12062085 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12062085 732874 Nr0b2 nuclear receptor subfamily 0, group B, member 2 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:12062085 732876 Gtpbp4 GTP binding protein 4 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20210128 MGI 732876 Gtpbp4 GTP binding protein 4 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220519 MGI 732876 Gtpbp4 GTP binding protein 4 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20241017 MGI 732876 Gtpbp4 GTP binding protein 4 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 732876 Gtpbp4 GTP binding protein 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 732876 Gtpbp4 GTP binding protein 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 732876 Gtpbp4 GTP binding protein 4 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20241017 MGI 732879 Rbm10 RNA binding motif protein 10 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 732879 Rbm10 RNA binding motif protein 10 gene MP:0000601 small liver IEA N RGD:5509061 20230601 MGI 732879 Rbm10 RNA binding motif protein 10 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 732879 Rbm10 RNA binding motif protein 10 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 732879 Rbm10 RNA binding motif protein 10 gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 732879 Rbm10 RNA binding motif protein 10 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 732879 Rbm10 RNA binding motif protein 10 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 732879 Rbm10 RNA binding motif protein 10 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 732879 Rbm10 RNA binding motif protein 10 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230601 MGI 732879 Rbm10 RNA binding motif protein 10 gene MP:0002989 small kidney IEA N RGD:5509061 20230601 MGI 732879 Rbm10 RNA binding motif protein 10 gene MP:0009084 blind uterus IEA N RGD:5509061 20230601 MGI 732881 Pacs1 phosphofurin acidic cluster sorting protein 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20190502 MGI 732881 Pacs1 phosphofurin acidic cluster sorting protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732884 Retnlg resistin like gamma gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 732884 Retnlg resistin like gamma gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 732885 Mmp8 matrix metallopeptidase 8 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:14517555 732885 Mmp8 matrix metallopeptidase 8 gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:14517555 732885 Mmp8 matrix metallopeptidase 8 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14517555 732885 Mmp8 matrix metallopeptidase 8 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15187163 732885 Mmp8 matrix metallopeptidase 8 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:14517555 732885 Mmp8 matrix metallopeptidase 8 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20210128 MGI 732885 Mmp8 matrix metallopeptidase 8 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 732885 Mmp8 matrix metallopeptidase 8 gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14517555 732887 Bik BCL2-interacting killer gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14749373 732887 Bik BCL2-interacting killer gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14749373 732887 Bik BCL2-interacting killer gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14749373 732887 Bik BCL2-interacting killer gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:14749373 732887 Bik BCL2-interacting killer gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:16270031 732887 Bik BCL2-interacting killer gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:14749373 732887 Bik BCL2-interacting killer gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:16270031 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21708930 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:20551902 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:21708930 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:20551902 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21708930 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:20551902 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:20551902 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21708930 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:20551902 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:21708930 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21708930 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21708930 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20551902 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20551902 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21708930 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0010228 decreased transitional stage T3 B cell number IAGP N RGD:5509061 20141003 MGI PMID:21708930 732891 Sh3kbp1 SH3-domain kinase binding protein 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:20551902 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15269275 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:15269275 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20240523 MGI 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15269275 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:15269275 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15269275 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15269275 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15269275 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:16436611 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15269275 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16436611 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:16436611 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:15269275 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:15269275 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15269275 732896 Rab3c RAB3C, member RAS oncogene family gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15269275 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20160915 MGI PMID:25698737 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20160915 MGI PMID:25698737 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20181108 MGI PMID:30157172 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20160915 MGI PMID:25698737 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20181227 MGI 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20160915 MGI PMID:25698737 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20160915 MGI PMID:25698737 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20181108 MGI PMID:30157172 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20181108 MGI PMID:30157172 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20181108 MGI PMID:30157172 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20181108 MGI PMID:30157172 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0003734 abnormal retina inner plexiform layer morphology IAGP N RGD:5509061 20181108 MGI PMID:30157172 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20160915 MGI PMID:25698737 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20160915 MGI PMID:25698737 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20181108 MGI PMID:30157172 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20160915 MGI PMID:25698737 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20160915 MGI PMID:25698737 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20160915 MGI PMID:25698737 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20160915 MGI PMID:25698737 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20181108 MGI PMID:30157172 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20181108 MGI PMID:30157172 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20181108 MGI PMID:30157172 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 732898 Clcc1 chloride channel CLIC-like 1 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20160922 MGI PMID:25698737 732899 Ppp2r2d protein phosphatase 2, regulatory subunit B, delta gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 732899 Ppp2r2d protein phosphatase 2, regulatory subunit B, delta gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 732899 Ppp2r2d protein phosphatase 2, regulatory subunit B, delta gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20210902 MGI PMID:32897879 732899 Ppp2r2d protein phosphatase 2, regulatory subunit B, delta gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20210902 MGI PMID:32897879 732901 Fbxo2 F-box protein 2 gene MP:0000032 cochlear degeneration IAGP N RGD:5509061 20141003 MGI PMID:17494702 732901 Fbxo2 F-box protein 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210520 MGI 732901 Fbxo2 F-box protein 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20160421 MGI 732901 Fbxo2 F-box protein 2 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:17494702 732901 Fbxo2 F-box protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210923 MGI PMID:34215698 732901 Fbxo2 F-box protein 2 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17494702 732901 Fbxo2 F-box protein 2 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:17494702 732901 Fbxo2 F-box protein 2 gene MP:0004300 abnormal organ of Corti supporting cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17494702 732901 Fbxo2 F-box protein 2 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17494702 732901 Fbxo2 F-box protein 2 gene MP:0004430 abnormal Claudius cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17494702 732901 Fbxo2 F-box protein 2 gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:17494702 732901 Fbxo2 F-box protein 2 gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:17494702 732901 Fbxo2 F-box protein 2 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20210128 MGI 732901 Fbxo2 F-box protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210923 MGI PMID:34215698 732901 Fbxo2 F-box protein 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20210923 MGI PMID:34215698 732901 Fbxo2 F-box protein 2 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:17494702 732901 Fbxo2 F-box protein 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17494702 732901 Fbxo2 F-box protein 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 732903 Slc1a6 solute carrier family 1 (high affinity aspartate/glutamate transporter), member 6 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:14715943 732904 Pmfbp1 polyamine modulated factor 1 binding protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20181220 MGI PMID:30032984 732904 Pmfbp1 polyamine modulated factor 1 binding protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20210422 MGI PMID:30298696 732904 Pmfbp1 polyamine modulated factor 1 binding protein 1 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20181220 MGI PMID:30032984 732904 Pmfbp1 polyamine modulated factor 1 binding protein 1 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20210422 MGI PMID:30298696 732904 Pmfbp1 polyamine modulated factor 1 binding protein 1 gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20181220 MGI PMID:30032984 732904 Pmfbp1 polyamine modulated factor 1 binding protein 1 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20181220 MGI PMID:30032984 732904 Pmfbp1 polyamine modulated factor 1 binding protein 1 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20210422 MGI PMID:30298696 732904 Pmfbp1 polyamine modulated factor 1 binding protein 1 gene MP:0014468 disorganized sperm mitochondrial sheath IAGP N RGD:5509061 20240613 MGI PMID:30298696 732906 Prpsap2 phosphoribosyl pyrophosphate synthetase-associated protein 2 gene MP:0002764 short tibia IEA N RGD:5509061 20141003 MGI 732910 Kcnmb4 potassium large conductance calcium-activated channel, subfamily M, beta member 4 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 732910 Kcnmb4 potassium large conductance calcium-activated channel, subfamily M, beta member 4 gene MP:0000948 nonconvulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:16261134 732910 Kcnmb4 potassium large conductance calcium-activated channel, subfamily M, beta member 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 732910 Kcnmb4 potassium large conductance calcium-activated channel, subfamily M, beta member 4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 732910 Kcnmb4 potassium large conductance calcium-activated channel, subfamily M, beta member 4 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 732910 Kcnmb4 potassium large conductance calcium-activated channel, subfamily M, beta member 4 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:16261134 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:15469964 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:11076674 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:11076674 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:11076674 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16651620 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11103935 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20160811 MGI 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000274 enlarged heart IEA N RGD:5509061 20160811 MGI 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22020437 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16023597 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20141003 MGI PMID:17848507 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000405 abnormal auchene hair morphology IAGP N RGD:5509061 20141003 MGI PMID:17848507 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:16322092 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000526 small inner medullary pyramid IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16488991 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18598944 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:18598944 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000621 increased salivary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11103935 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20160811 MGI 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11103935 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10881179 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:11076674 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20160811 MGI 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001147 small testis IEA N RGD:5509061 20160811 MGI 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001204 decreased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:10514395 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15469964 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16014817 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15154924 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18598944 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:12810620 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:11076674 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:11076674 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:23657012 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:22241836 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:22241836 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21258009 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11103935 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11076674 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12810620 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14647411 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11103935 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11280729 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21331045 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002083 premature death IAGP N RGD:5509061 20160915 MGI PMID:21368895 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11076674 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:15469964 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16651620 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:9887329 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:16322092 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002607 decreased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:14767984 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:15469964 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20160811 MGI 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:16014817 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003010 decreased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003010 decreased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:21724834 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9887329 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003075 abnormal response to CNS ischemic injury IAGP N RGD:5509061 20141003 MGI PMID:15067031 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:7664346 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11076674 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14767984 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18598944 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:16651620 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11551927 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003613 abnormal kidney medulla development IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:16908765 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18598944 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003763 abnormal thymus physiology IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:16651620 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18598944 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18598944 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:15469964 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20141003 MGI PMID:11551927 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:15469964 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22241836 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20141003 MGI PMID:10508513 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:11076674 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:17287518 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:10921903 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:16023597 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:10508513 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20571512 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20160304 MGI PMID:25196150 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23657012 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11551927 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004353 abnormal deltoid tuberosity morphology IAGP N RGD:5509061 20141003 MGI PMID:11076674 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:11076674 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17287518 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:17287518 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:17287518 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004407 increased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:17287518 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004408 decreased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:17287518 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004432 abnormal cochlear hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17287518 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:12466968 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:12810620 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004503 decreased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:11076674 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:10710306 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:16014817 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20160811 MGI 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:15067031 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:15067031 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005005 abnormal self tolerance IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:16322092 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15469964 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15469964 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15469964 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16908765 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:11551927 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9887329 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:16908765 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11551927 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22020437 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:15889143 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20571512 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:11551927 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:16908765 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:16322092 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:11076674 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:11076674 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008409 increased cellular sensitivity to hydroxyurea IAGP N RGD:5509061 20141003 MGI PMID:10921903 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:10921903 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:12952892 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:15917306 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008538 decreased zigzag hair amount IAGP N RGD:5509061 20141003 MGI PMID:17848507 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008542 enlarged cervical lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10655105 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10571777 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16322092 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21331045 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:12952892 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:15067031 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:18598944 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0009130 increased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:15469964 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15469964 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0009300 increased parametrial fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15469964 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0009381 abnormal prostate gland dorsolateral lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:16014817 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16488991 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0009550 increased urinary bladder carcinoma incidence IAGP N RGD:5509061 20160915 MGI PMID:21368895 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11551927 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0009592 increased Leydig cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10710306 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16908765 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10710306 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15469964 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14647411 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0010289 increased urinary system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:11103935 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0010384 increased renal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18598944 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20160304 MGI PMID:25196150 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20160304 MGI PMID:25196150 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10710306 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21885021 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160304 MGI PMID:25196150 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12533509 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22241836 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9207798 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23657012 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9925645 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0011512 mesangial cell interposition IAGP N RGD:5509061 20141003 MGI PMID:11970874 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:10508513 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:16023597 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20160304 MGI PMID:25196150 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:15469964 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0013383 increased sebaceous gland adenoma incidence IAGP N RGD:5509061 20141218 MGI PMID:11507077 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0013443 Harderian gland hyperplasia IAGP N RGD:5509061 20150205 MGI PMID:11103935 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0013446 enlarged Harderian gland IAGP N RGD:5509061 20150205 MGI PMID:11103935 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0021085 increased DNA replication IAGP N RGD:5509061 20220310 MGI PMID:10571777 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0021155 abnormal heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:25196150 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0030516 abnormal junctional epithelium morphology IAGP N RGD:5509061 20180111 MGI PMID:15154924 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0031359 decreased prostate gland anterior lobe weight IAGP N RGD:5509061 20220303 MGI PMID:16014817 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0031362 decreased prostate gland ventral lobe weight IAGP N RGD:5509061 20220303 MGI PMID:16014817 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0031366 decreased prostate gland dorsolateral lobe weight IAGP N RGD:5509061 20220303 MGI PMID:16014817 732911 Cdkn1a cyclin dependent kinase inhibitor 1A gene MP:0031510 increased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:16908765 732913 Prkch protein kinase C, eta gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12750259 732913 Prkch protein kinase C, eta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12750259 732913 Prkch protein kinase C, eta gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:12750259 732913 Prkch protein kinase C, eta gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:12750259 732913 Prkch protein kinase C, eta gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0002351 abnormal cervical lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:12750259 732913 Prkch protein kinase C, eta gene MP:0003671 abnormal eyelid aperture IAGP N RGD:5509061 20141003 MGI PMID:12750259 732913 Prkch protein kinase C, eta gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220811 MGI 732913 Prkch protein kinase C, eta gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:12750259 732913 Prkch protein kinase C, eta gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0005231 abnormal brachial lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0008542 enlarged cervical lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0009623 enlarged inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0009631 enlarged axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210422 MGI 732913 Prkch protein kinase C, eta gene MP:0010130 decreased DN1 thymic pro-T cell number IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22155788 732913 Prkch protein kinase C, eta gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12750259 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22099461 732914 Sh3gl1 SH3-domain GRB2-like 1 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:22099461 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0000120 malocclusion IEA N RGD:5509061 20161020 MGI 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:22272310 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:14622583 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:22272310 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22272310 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0001265 decreased body size IEA N RGD:5509061 20161020 MGI 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22272310 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0001406 abnormal gait IEA N RGD:5509061 20161020 MGI 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:22272310 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:14622583 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:14622583 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0001921 reduced fertility IEA N RGD:5509061 20161020 MGI 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0002083 premature death IEA N RGD:5509061 20161020 MGI 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:14622583 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0002826 tonic seizures IEA N RGD:5509061 20161020 MGI 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:14622583 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0003049 abnormal lumbar vertebrae morphology IEA N RGD:5509061 20210826 MGI 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0003050 abnormal sacral vertebrae morphology IEA N RGD:5509061 20210826 MGI 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:14622583 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:22272310 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22272310 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0005604 hyperekplexia IAGP N RGD:5509061 20141003 MGI PMID:14622583 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:14622583 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:14622583 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0010769 abnormal survival IEA N RGD:5509061 20161020 MGI 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0010831 lethality, incomplete penetrance IEA N RGD:5509061 20161020 MGI 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0011084 lethality at weaning, incomplete penetrance IEA N RGD:5509061 20161020 MGI 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14622583 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22272310 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0011396 abnormal sleep behavior IAGP N RGD:5509061 20141003 MGI PMID:22272310 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:14622583 732916 Slc6a5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:14622583 732917 Stx3 syntaxin 3 gene MP:0008763 abnormal mast cell degranulation IAGP N RGD:5509061 20230518 MGI PMID:30563839 732917 Stx3 syntaxin 3 gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20230518 MGI PMID:30563839 732917 Stx3 syntaxin 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 732917 Stx3 syntaxin 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230518 MGI PMID:30563839 732917 Stx3 syntaxin 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732917 Stx3 syntaxin 3 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 732917 Stx3 syntaxin 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220519 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:11356028 732920 Neurod2 neurogenic differentiation 2 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:11356028 732920 Neurod2 neurogenic differentiation 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11356028 732920 Neurod2 neurogenic differentiation 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20240523 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0001314 cornea opacity IEA N RGD:5509061 20240523 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20201022 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20200514 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11356028 732920 Neurod2 neurogenic differentiation 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11356028 732920 Neurod2 neurogenic differentiation 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20200514 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20201022 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11356028 732920 Neurod2 neurogenic differentiation 2 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:11356028 732920 Neurod2 neurogenic differentiation 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210826 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20210826 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11356028 732920 Neurod2 neurogenic differentiation 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11356028 732920 Neurod2 neurogenic differentiation 2 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20210128 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20201022 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:11356028 732920 Neurod2 neurogenic differentiation 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:11356028 732920 Neurod2 neurogenic differentiation 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201022 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0005287 narrow eye opening IEA N RGD:5509061 20240523 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0005544 cornea deposits IEA N RGD:5509061 20240523 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20240523 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20230601 MGI 732920 Neurod2 neurogenic differentiation 2 gene MP:0011940 decreased food intake IEA N RGD:5509061 20201022 MGI 732922 Clic5 chloride intracellular channel 5 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021174 732922 Clic5 chloride intracellular channel 5 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 732922 Clic5 chloride intracellular channel 5 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0000505 decreased digestive secretion IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0001258 decreased body length IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0001394 circling IEA N RGD:5509061 20170302 MGI 732922 Clic5 chloride intracellular channel 5 gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:17021174 732922 Clic5 chloride intracellular channel 5 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:17021174 732922 Clic5 chloride intracellular channel 5 gene MP:0001410 head bobbing IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0001433 polyphagia IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20190502 MGI 732922 Clic5 chloride intracellular channel 5 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:17021174 732922 Clic5 chloride intracellular channel 5 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:17021174 732922 Clic5 chloride intracellular channel 5 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20190207 MGI PMID:20335315 732922 Clic5 chloride intracellular channel 5 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:17021174 732922 Clic5 chloride intracellular channel 5 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021174 732922 Clic5 chloride intracellular channel 5 gene MP:0002871 albuminuria IAGP N RGD:5509061 20190207 MGI PMID:20335315 732922 Clic5 chloride intracellular channel 5 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20190207 MGI PMID:20664558 732922 Clic5 chloride intracellular channel 5 gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021174 732922 Clic5 chloride intracellular channel 5 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021174 732922 Clic5 chloride intracellular channel 5 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17021174 732922 Clic5 chloride intracellular channel 5 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:17021174 732922 Clic5 chloride intracellular channel 5 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20190207 MGI PMID:20335315 732922 Clic5 chloride intracellular channel 5 gene MP:0005202 lethargy IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0005307 head tossing IEA N RGD:5509061 20170302 MGI 732922 Clic5 chloride intracellular channel 5 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20190207 MGI PMID:20335315 732922 Clic5 chloride intracellular channel 5 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20190207 MGI PMID:29425878 732922 Clic5 chloride intracellular channel 5 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0006359 absent startle reflex IEA N RGD:5509061 20170302 MGI 732922 Clic5 chloride intracellular channel 5 gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20190207 MGI PMID:20335315 732922 Clic5 chloride intracellular channel 5 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20190207 MGI PMID:20664558 732922 Clic5 chloride intracellular channel 5 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20190207 MGI PMID:20335315 732922 Clic5 chloride intracellular channel 5 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20190502 MGI 732922 Clic5 chloride intracellular channel 5 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20190207 MGI PMID:20357015 732922 Clic5 chloride intracellular channel 5 gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20190207 MGI PMID:20335315 732922 Clic5 chloride intracellular channel 5 gene MP:0011454 abnormal glomerular endothelium fenestra morphology IAGP N RGD:5509061 20190207 MGI PMID:20335315 732922 Clic5 chloride intracellular channel 5 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17021174 732922 Clic5 chloride intracellular channel 5 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:20357015 732923 Zp2 zona pellucida glycoprotein 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:12852850 732923 Zp2 zona pellucida glycoprotein 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12852850 732923 Zp2 zona pellucida glycoprotein 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11245577 732923 Zp2 zona pellucida glycoprotein 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12852850 732923 Zp2 zona pellucida glycoprotein 2 gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:12852850 732923 Zp2 zona pellucida glycoprotein 2 gene MP:0009372 abnormal cumulus oophorus morphology IAGP N RGD:5509061 20141003 MGI PMID:11245577 732923 Zp2 zona pellucida glycoprotein 2 gene MP:0009375 thin zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:11245577 732923 Zp2 zona pellucida glycoprotein 2 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:11245577 732923 Zp2 zona pellucida glycoprotein 2 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220804 MGI PMID:11245577 732925 Xpo1 exportin 1 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 732925 Xpo1 exportin 1 gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 732925 Xpo1 exportin 1 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 732925 Xpo1 exportin 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 732925 Xpo1 exportin 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 732925 Xpo1 exportin 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 732925 Xpo1 exportin 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 732925 Xpo1 exportin 1 gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 732925 Xpo1 exportin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732925 Xpo1 exportin 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 732925 Xpo1 exportin 1 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20231207 MGI 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20181227 MGI 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:19193906 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19193906 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0001785 edema IEA N RGD:5509061 20221103 MGI 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:19193906 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19193906 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20201022 MGI 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19193906 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0008823 abnormal interventricular septum membranous part morphology IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0010498 abnormal interventricular septum muscular part morphology IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0011514 skin hemorrhage IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0013848 subcutaneous edema IAGP N RGD:5509061 20190926 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0031589 detached epicardium IAGP N RGD:5509061 20240229 MGI PMID:28067313 732927 Baiap2 brain-specific angiogenesis inhibitor 1-associated protein 2 gene MP:0031591 detached endocardium IAGP N RGD:5509061 20240229 MGI PMID:28067313 732929 Coro1a coronin, actin binding protein 1A gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18345003 732929 Coro1a coronin, actin binding protein 1A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9449705 732929 Coro1a coronin, actin binding protein 1A gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17548658 732929 Coro1a coronin, actin binding protein 1A gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9449705 732929 Coro1a coronin, actin binding protein 1A gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:18836449 732929 Coro1a coronin, actin binding protein 1A gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:18836449 732929 Coro1a coronin, actin binding protein 1A gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 732929 Coro1a coronin, actin binding protein 1A gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:17632055 732929 Coro1a coronin, actin binding protein 1A gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18345003 732929 Coro1a coronin, actin binding protein 1A gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18836449 732929 Coro1a coronin, actin binding protein 1A gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17548658 732929 Coro1a coronin, actin binding protein 1A gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17632055 732929 Coro1a coronin, actin binding protein 1A gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18836449 732929 Coro1a coronin, actin binding protein 1A gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18836449 732929 Coro1a coronin, actin binding protein 1A gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:17548658 732929 Coro1a coronin, actin binding protein 1A gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:16902139 732929 Coro1a coronin, actin binding protein 1A gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:17548658 732929 Coro1a coronin, actin binding protein 1A gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:18345003 732929 Coro1a coronin, actin binding protein 1A gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:17548658 732929 Coro1a coronin, actin binding protein 1A gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:17548658 732929 Coro1a coronin, actin binding protein 1A gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17548658 732929 Coro1a coronin, actin binding protein 1A gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17548658 732929 Coro1a coronin, actin binding protein 1A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18345003 732929 Coro1a coronin, actin binding protein 1A gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16902139 732929 Coro1a coronin, actin binding protein 1A gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18345003 732929 Coro1a coronin, actin binding protein 1A gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:21844203 732929 Coro1a coronin, actin binding protein 1A gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18836449 732929 Coro1a coronin, actin binding protein 1A gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16902139 732929 Coro1a coronin, actin binding protein 1A gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16902139 732929 Coro1a coronin, actin binding protein 1A gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18345003 732929 Coro1a coronin, actin binding protein 1A gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18836449 732929 Coro1a coronin, actin binding protein 1A gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16902139 732929 Coro1a coronin, actin binding protein 1A gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18345003 732929 Coro1a coronin, actin binding protein 1A gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18836449 732929 Coro1a coronin, actin binding protein 1A gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21844203 732929 Coro1a coronin, actin binding protein 1A gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:18345003 732929 Coro1a coronin, actin binding protein 1A gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21844203 732929 Coro1a coronin, actin binding protein 1A gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:21844203 732936 Fzd3 frizzled class receptor 3 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:16495441 732936 Fzd3 frizzled class receptor 3 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20141003 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:21746835 732936 Fzd3 frizzled class receptor 3 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:21746835 732936 Fzd3 frizzled class receptor 3 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16495441 732936 Fzd3 frizzled class receptor 3 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:14671310 732936 Fzd3 frizzled class receptor 3 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:16495441 732936 Fzd3 frizzled class receptor 3 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:16495441 732936 Fzd3 frizzled class receptor 3 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 732936 Fzd3 frizzled class receptor 3 gene MP:0002635 reduced sensorimotor gating IAGP N RGD:5509061 20141003 MGI PMID:21746835 732936 Fzd3 frizzled class receptor 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16495441 732936 Fzd3 frizzled class receptor 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:16495441 732936 Fzd3 frizzled class receptor 3 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16495441 732936 Fzd3 frizzled class receptor 3 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:16495441 732936 Fzd3 frizzled class receptor 3 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16495441 732936 Fzd3 frizzled class receptor 3 gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16495441 732936 Fzd3 frizzled class receptor 3 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20160421 MGI 732936 Fzd3 frizzled class receptor 3 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0008129 absent brain internal capsule IAGP N RGD:5509061 20141003 MGI PMID:14671310 732936 Fzd3 frizzled class receptor 3 gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:21746835 732936 Fzd3 frizzled class receptor 3 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21746835 732936 Fzd3 frizzled class receptor 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 732936 Fzd3 frizzled class receptor 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 732936 Fzd3 frizzled class receptor 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 732936 Fzd3 frizzled class receptor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16495441 732936 Fzd3 frizzled class receptor 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 732936 Fzd3 frizzled class receptor 3 gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:12351730 732936 Fzd3 frizzled class receptor 3 gene MP:0014413 decreased depression-related behavior IAGP N RGD:5509061 20240425 MGI PMID:21746835 732938 Stau2 staufen double-stranded RNA binding protein 2 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20201022 MGI 732938 Stau2 staufen double-stranded RNA binding protein 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 732938 Stau2 staufen double-stranded RNA binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20201217 MGI PMID:30979012 732938 Stau2 staufen double-stranded RNA binding protein 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20201217 MGI PMID:30979012 732938 Stau2 staufen double-stranded RNA binding protein 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 732938 Stau2 staufen double-stranded RNA binding protein 2 gene MP:0002608 increased hematocrit IEA N RGD:5509061 20210128 MGI 732938 Stau2 staufen double-stranded RNA binding protein 2 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20201217 MGI PMID:30979012 732938 Stau2 staufen double-stranded RNA binding protein 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 732938 Stau2 staufen double-stranded RNA binding protein 2 gene MP:0004997 increased CNS synapse formation IAGP N RGD:5509061 20201217 MGI PMID:30979012 732938 Stau2 staufen double-stranded RNA binding protein 2 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 732938 Stau2 staufen double-stranded RNA binding protein 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20181227 MGI 732938 Stau2 staufen double-stranded RNA binding protein 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 732941 Ythdc1 YTH domain containing 1 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20180830 MGI PMID:29799838 732941 Ythdc1 YTH domain containing 1 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20180830 MGI PMID:29799838 732941 Ythdc1 YTH domain containing 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20180830 MGI PMID:29799838 732941 Ythdc1 YTH domain containing 1 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20180830 MGI PMID:29799838 732941 Ythdc1 YTH domain containing 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20180830 MGI PMID:29799838 732941 Ythdc1 YTH domain containing 1 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20180830 MGI PMID:29799838 732941 Ythdc1 YTH domain containing 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180830 MGI PMID:29799838 732941 Ythdc1 YTH domain containing 1 gene MP:0011130 absent tertiary ovarian follicles IAGP N RGD:5509061 20180830 MGI PMID:29799838 732941 Ythdc1 YTH domain containing 1 gene MP:0020845 abnormal DNA-templated transcription IAGP N RGD:5509061 20180830 MGI PMID:29799838 732941 Ythdc1 YTH domain containing 1 gene MP:0031382 absent secondary ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:29799838 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12775763 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12551946 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:12551946 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12775763 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12551946 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12551946 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12775763 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12551946 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0002673 abnormal sperm number IAGP N RGD:5509061 20141003 MGI PMID:12775763 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12551946 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12775763 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12551946 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12775763 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:12551946 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12551946 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:12551946 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12775763 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:12551946 732943 Pafah1b3 platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:12775763 732945 Cd48 CD48 antigen gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:9927686 732945 Cd48 CD48 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9927686 732945 Cd48 CD48 antigen gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9927686 732946 Lgals2 lectin, galactose-binding, soluble 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 732946 Lgals2 lectin, galactose-binding, soluble 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 732946 Lgals2 lectin, galactose-binding, soluble 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20150226 MGI PMID:23118208 732946 Lgals2 lectin, galactose-binding, soluble 2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 732946 Lgals2 lectin, galactose-binding, soluble 2 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 732946 Lgals2 lectin, galactose-binding, soluble 2 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20150226 MGI PMID:23118208 732946 Lgals2 lectin, galactose-binding, soluble 2 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20150226 MGI PMID:23118208 732946 Lgals2 lectin, galactose-binding, soluble 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 732946 Lgals2 lectin, galactose-binding, soluble 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20150226 MGI PMID:23118208 732946 Lgals2 lectin, galactose-binding, soluble 2 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20150226 MGI PMID:23118208 732946 Lgals2 lectin, galactose-binding, soluble 2 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20150226 MGI PMID:23118208 732946 Lgals2 lectin, galactose-binding, soluble 2 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20150226 MGI PMID:23118208 732946 Lgals2 lectin, galactose-binding, soluble 2 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20150226 MGI PMID:23118208 732946 Lgals2 lectin, galactose-binding, soluble 2 gene MP:0020155 enhanced humoral immune response IAGP N RGD:5509061 20150226 MGI PMID:23118208 732949 Ufd1 ubiquitin recognition factor in ER-associated degradation 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10517636 732950 Hrh4 histamine receptor H4 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16709868 732950 Hrh4 histamine receptor H4 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16709868 732950 Hrh4 histamine receptor H4 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12626656 732950 Hrh4 histamine receptor H4 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16709868 732950 Hrh4 histamine receptor H4 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16709868 732950 Hrh4 histamine receptor H4 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20201022 MGI 732950 Hrh4 histamine receptor H4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16709868 732950 Hrh4 histamine receptor H4 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:16709868 732950 Hrh4 histamine receptor H4 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:16709868 732950 Hrh4 histamine receptor H4 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20210128 MGI 732950 Hrh4 histamine receptor H4 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 732951 Ap2m1 adaptor-related protein complex 2, mu 1 subunit gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16227583 732951 Ap2m1 adaptor-related protein complex 2, mu 1 subunit gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16227583 732953 Slc22a8 solute carrier family 22 (organic anion transporter), member 8 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 732953 Slc22a8 solute carrier family 22 (organic anion transporter), member 8 gene MP:0006272 abnormal urine organic anion level IAGP N RGD:5509061 20141003 MGI PMID:12011098 732953 Slc22a8 solute carrier family 22 (organic anion transporter), member 8 gene MP:0011424 decreased urine uric acid level IAGP N RGD:5509061 20141003 MGI PMID:18270321 732955 Dusp1 dual specificity phosphatase 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:20483921 732955 Dusp1 dual specificity phosphatase 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:20371627 732955 Dusp1 dual specificity phosphatase 1 gene MP:0000750 abnormal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:20371627 732955 Dusp1 dual specificity phosphatase 1 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:20371627 732955 Dusp1 dual specificity phosphatase 1 gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20702711 732955 Dusp1 dual specificity phosphatase 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:16380513 732955 Dusp1 dual specificity phosphatase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20371627 732955 Dusp1 dual specificity phosphatase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20483921 732955 Dusp1 dual specificity phosphatase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20371627 732955 Dusp1 dual specificity phosphatase 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20953200 732955 Dusp1 dual specificity phosphatase 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0001573 abnormal circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:16380513 732955 Dusp1 dual specificity phosphatase 1 gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:16380513 732955 Dusp1 dual specificity phosphatase 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:16380513 732955 Dusp1 dual specificity phosphatase 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:20483921 732955 Dusp1 dual specificity phosphatase 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20483921 732955 Dusp1 dual specificity phosphatase 1 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20141003 MGI PMID:16424221 732955 Dusp1 dual specificity phosphatase 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 732955 Dusp1 dual specificity phosphatase 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16380513 732955 Dusp1 dual specificity phosphatase 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20702711 732955 Dusp1 dual specificity phosphatase 1 gene MP:0003213 decreased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:20953200 732955 Dusp1 dual specificity phosphatase 1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:16424221 732955 Dusp1 dual specificity phosphatase 1 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:16380513 732955 Dusp1 dual specificity phosphatase 1 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16380513 732955 Dusp1 dual specificity phosphatase 1 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:20371627 732955 Dusp1 dual specificity phosphatase 1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:17636038 732955 Dusp1 dual specificity phosphatase 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16380513 732955 Dusp1 dual specificity phosphatase 1 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:17636038 732955 Dusp1 dual specificity phosphatase 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16380513 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:20935641 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16380512 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16424221 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16380512 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:16424221 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:16380512 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:16424221 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:16380512 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:16424221 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20483921 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:16380512 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20483921 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:16424221 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20483921 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16380512 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16424221 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:16424221 732955 Dusp1 dual specificity phosphatase 1 gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:17636038 732955 Dusp1 dual specificity phosphatase 1 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0009287 decreased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:20371627 732955 Dusp1 dual specificity phosphatase 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:20371627 732955 Dusp1 dual specificity phosphatase 1 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:20371627 732955 Dusp1 dual specificity phosphatase 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16380513 732955 Dusp1 dual specificity phosphatase 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16380512 732955 Dusp1 dual specificity phosphatase 1 gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:16424221 732955 Dusp1 dual specificity phosphatase 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20371627 732955 Dusp1 dual specificity phosphatase 1 gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:20371627 732955 Dusp1 dual specificity phosphatase 1 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20190725 MGI PMID:20371627 732955 Dusp1 dual specificity phosphatase 1 gene MP:0020102 increased hepatic glucose production IAGP N RGD:5509061 20200102 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0030948 decreased myoblast proliferation IAGP N RGD:5509061 20190725 MGI PMID:20371627 732955 Dusp1 dual specificity phosphatase 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:16814733 732955 Dusp1 dual specificity phosphatase 1 gene MP:0031270 decreased susceptibility to age-related hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:16814733 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:23153828 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:10642554 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:11986227 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0004041 increased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:16444293 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10642554 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16444293 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19136662 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19136662 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10642554 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:10642554 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:18524992 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16444293 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19136662 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19136662 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19136662 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20231207 MGI 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10642554 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732956 Cr1l complement C3b/C4b receptor 1 like gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 732960 Epha7 Eph receptor A7 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:11089974 732960 Epha7 Eph receptor A7 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15713841 732960 Epha7 Eph receptor A7 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:15996548 732964 Lhx1 LIM homeobox protein 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20151231 MGI PMID:26494787 732964 Lhx1 LIM homeobox protein 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20151231 MGI PMID:26494787 732964 Lhx1 LIM homeobox protein 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20151231 MGI PMID:26494787 732964 Lhx1 LIM homeobox protein 1 gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20151231 MGI PMID:26494787 732964 Lhx1 LIM homeobox protein 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:15857913 732964 Lhx1 LIM homeobox protein 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:16216236 732964 Lhx1 LIM homeobox protein 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:16216236 732964 Lhx1 LIM homeobox protein 1 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10529425 732964 Lhx1 LIM homeobox protein 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10529425 732964 Lhx1 LIM homeobox protein 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17664423 732964 Lhx1 LIM homeobox protein 1 gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:17664423 732964 Lhx1 LIM homeobox protein 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:17664423 732964 Lhx1 LIM homeobox protein 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20151231 MGI PMID:26494787 732964 Lhx1 LIM homeobox protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:10529425 732964 Lhx1 LIM homeobox protein 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16216236 732964 Lhx1 LIM homeobox protein 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10862151 732964 Lhx1 LIM homeobox protein 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10529425 732964 Lhx1 LIM homeobox protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10748463 732964 Lhx1 LIM homeobox protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15857913 732964 Lhx1 LIM homeobox protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17664423 732964 Lhx1 LIM homeobox protein 1 gene MP:0002174 abnormal gastrulation movements IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:11291865 732964 Lhx1 LIM homeobox protein 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:16600854 732964 Lhx1 LIM homeobox protein 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 732964 Lhx1 LIM homeobox protein 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:16216236 732964 Lhx1 LIM homeobox protein 1 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16216236 732964 Lhx1 LIM homeobox protein 1 gene MP:0003557 absent vas deferens IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0003558 absent uterus IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0003578 absent ovary IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:16216236 732964 Lhx1 LIM homeobox protein 1 gene MP:0003613 abnormal kidney medulla development IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0003826 abnormal Mullerian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16216236 732964 Lhx1 LIM homeobox protein 1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20151231 MGI PMID:26494787 732964 Lhx1 LIM homeobox protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15857913 732964 Lhx1 LIM homeobox protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20151231 MGI PMID:26494787 732964 Lhx1 LIM homeobox protein 1 gene MP:0004017 duplex kidney IAGP N RGD:5509061 20141003 MGI PMID:16216236 732964 Lhx1 LIM homeobox protein 1 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20151231 MGI PMID:26494787 732964 Lhx1 LIM homeobox protein 1 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15857913 732964 Lhx1 LIM homeobox protein 1 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20151231 MGI PMID:26494787 732964 Lhx1 LIM homeobox protein 1 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0004557 dilated allantois IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0004559 small allantois IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0004727 absent epididymis IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:16216236 732964 Lhx1 LIM homeobox protein 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:11291865 732964 Lhx1 LIM homeobox protein 1 gene MP:0005644 agonadal IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0006415 absent testes IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0006425 absent Mullerian ducts IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0006426 Mullerian duct degeneration IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0009074 Wolffian duct degeneration IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0009074 Wolffian duct degeneration IAGP N RGD:5509061 20141003 MGI PMID:16216236 732964 Lhx1 LIM homeobox protein 1 gene MP:0009075 rudimentary Wolffian ducts IAGP N RGD:5509061 20141003 MGI PMID:16216236 732964 Lhx1 LIM homeobox protein 1 gene MP:0009076 rudimentary Mullerian ducts IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0009076 rudimentary Mullerian ducts IAGP N RGD:5509061 20141003 MGI PMID:16216236 732964 Lhx1 LIM homeobox protein 1 gene MP:0009579 acephaly IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0009718 absent Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:17664423 732964 Lhx1 LIM homeobox protein 1 gene MP:0010982 abnormal ureteric bud elongation IAGP N RGD:5509061 20141003 MGI PMID:16216236 732964 Lhx1 LIM homeobox protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16216236 732964 Lhx1 LIM homeobox protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17664423 732964 Lhx1 LIM homeobox protein 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10862151 732964 Lhx1 LIM homeobox protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0011292 absent nephron IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0011354 absent renal glomerulus IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0011365 small metanephros IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0011366 absent metanephros IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0011486 ectopic ureter IAGP N RGD:5509061 20141003 MGI PMID:15930111 732964 Lhx1 LIM homeobox protein 1 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:10862151 732964 Lhx1 LIM homeobox protein 1 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:10862151 732964 Lhx1 LIM homeobox protein 1 gene MP:0012135 embryonic-extraembryonic boundary constriction IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:10862151 732964 Lhx1 LIM homeobox protein 1 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0012156 rostral-caudal axis duplication IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0012276 absent prechordal mesoderm IAGP N RGD:5509061 20141003 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:10862151 732964 Lhx1 LIM homeobox protein 1 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:11291865 732964 Lhx1 LIM homeobox protein 1 gene MP:0030324 abnormal anterior head development IAGP N RGD:5509061 20171109 MGI PMID:10862151 732964 Lhx1 LIM homeobox protein 1 gene MP:0030324 abnormal anterior head development IAGP N RGD:5509061 20171109 MGI PMID:7700351 732964 Lhx1 LIM homeobox protein 1 gene MP:0030324 abnormal anterior head development IAGP N RGD:5509061 20180118 MGI PMID:15930111 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0001147 small testis IAGP N RGD:5509061 20211209 MGI PMID:30998386 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20211209 MGI PMID:30998386 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10191063 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:10191063 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:10191063 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10191063 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10191063 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20211209 MGI PMID:30998386 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20150212 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20211209 MGI PMID:30998386 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20211209 MGI PMID:30998386 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20211209 MGI PMID:30998386 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20211209 MGI PMID:30998386 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20211209 MGI PMID:30998386 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20211209 MGI PMID:30998386 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20211209 MGI PMID:30998386 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20211209 MGI PMID:30998386 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20211209 MGI PMID:30998386 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:19103743 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:21390131 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20211209 MGI PMID:30998386 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10191063 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10191063 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0011594 decreased catalase activity IAGP N RGD:5509061 20211209 MGI PMID:30998386 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20211209 MGI PMID:30998386 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:19633665 732969 Xrcc1 X-ray repair complementing defective repair in Chinese hamster cells 1 gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20211209 MGI PMID:30998386 732971 Itgae integrin alpha E, epithelial-associated gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20160421 MGI 732971 Itgae integrin alpha E, epithelial-associated gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20181227 MGI 732971 Itgae integrin alpha E, epithelial-associated gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20181227 MGI 732971 Itgae integrin alpha E, epithelial-associated gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20181227 MGI 732971 Itgae integrin alpha E, epithelial-associated gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10352281 732971 Itgae integrin alpha E, epithelial-associated gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10352281 732971 Itgae integrin alpha E, epithelial-associated gene MP:0012361 decreased large unstained cell number IEA N RGD:5509061 20201022 MGI 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23263987 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23263987 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23263987 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:23263987 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20516079 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:23363625 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23263987 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23263987 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23263987 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:23263987 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23263987 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23263987 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23263987 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:23825225 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20141003 MGI PMID:23263987 732974 Rapgef3 Rap guanine nucleotide exchange factor (GEF) 3 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:23263987 732977 Ltb4r2 leukotriene B4 receptor 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23624557 732977 Ltb4r2 leukotriene B4 receptor 2 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18378794 732977 Ltb4r2 leukotriene B4 receptor 2 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20656922 732977 Ltb4r2 leukotriene B4 receptor 2 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23624557 732980 Psmc2 proteasome (prosome, macropain) 26S subunit, ATPase 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 732980 Psmc2 proteasome (prosome, macropain) 26S subunit, ATPase 2 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 732980 Psmc2 proteasome (prosome, macropain) 26S subunit, ATPase 2 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 732980 Psmc2 proteasome (prosome, macropain) 26S subunit, ATPase 2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20181227 MGI 732980 Psmc2 proteasome (prosome, macropain) 26S subunit, ATPase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732982 Tpp1 tripeptidyl peptidase I gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15483130 732982 Tpp1 tripeptidyl peptidase I gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:18343701 732982 Tpp1 tripeptidyl peptidase I gene MP:0000746 weakness IEA N RGD:5509061 20111116 MGI 732982 Tpp1 tripeptidyl peptidase I gene MP:0000751 myopathy IEA N RGD:5509061 20141003 MGI 732982 Tpp1 tripeptidyl peptidase I gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15483130 732982 Tpp1 tripeptidyl peptidase I gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18343701 732982 Tpp1 tripeptidyl peptidase I gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:15483130 732982 Tpp1 tripeptidyl peptidase I gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15483130 732982 Tpp1 tripeptidyl peptidase I gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18343701 732982 Tpp1 tripeptidyl peptidase I gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15483130 732982 Tpp1 tripeptidyl peptidase I gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15483130 732982 Tpp1 tripeptidyl peptidase I gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18343701 732982 Tpp1 tripeptidyl peptidase I gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:18343701 732982 Tpp1 tripeptidyl peptidase I gene MP:0001429 dehydration IEA N RGD:5509061 20111116 MGI 732982 Tpp1 tripeptidyl peptidase I gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:15483130 732982 Tpp1 tripeptidyl peptidase I gene MP:0001505 hunched posture IEA N RGD:5509061 20111116 MGI 732982 Tpp1 tripeptidyl peptidase I gene MP:0001954 respiratory distress IEA N RGD:5509061 20111116 MGI 732982 Tpp1 tripeptidyl peptidase I gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 732982 Tpp1 tripeptidyl peptidase I gene MP:0002064 seizures IEA N RGD:5509061 20111116 MGI 732982 Tpp1 tripeptidyl peptidase I gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20111116 MGI 732982 Tpp1 tripeptidyl peptidase I gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15483130 732982 Tpp1 tripeptidyl peptidase I gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18343701 732982 Tpp1 tripeptidyl peptidase I gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:18343701 732982 Tpp1 tripeptidyl peptidase I gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:15483130 732982 Tpp1 tripeptidyl peptidase I gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:15483130 732982 Tpp1 tripeptidyl peptidase I gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:15483130 732982 Tpp1 tripeptidyl peptidase I gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:18343701 732982 Tpp1 tripeptidyl peptidase I gene MP:0003313 abnormal locomotor activation IEA N RGD:5509061 20111116 MGI 732982 Tpp1 tripeptidyl peptidase I gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20141003 MGI PMID:18343701 732982 Tpp1 tripeptidyl peptidase I gene MP:0005426 tachypnea IEA N RGD:5509061 20111116 MGI 732982 Tpp1 tripeptidyl peptidase I gene MP:0011975 neuronal cytoplasmic inclusions IEA N RGD:5509061 20141003 MGI 732991 Ppib peptidylprolyl isomerase B gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19997487 732991 Ppib peptidylprolyl isomerase B gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:19997487 732991 Ppib peptidylprolyl isomerase B gene MP:0000066 osteoporosis IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19997487 732991 Ppib peptidylprolyl isomerase B gene MP:0000160 kyphosis IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0000547 short limbs IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19997487 732991 Ppib peptidylprolyl isomerase B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0001265 decreased body size IAGP N RGD:5509061 20151217 MGI PMID:19997487 732991 Ppib peptidylprolyl isomerase B gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19997487 732991 Ppib peptidylprolyl isomerase B gene MP:0002764 short tibia IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20151217 MGI PMID:19997487 732991 Ppib peptidylprolyl isomerase B gene MP:0003109 short femur IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:19997487 732991 Ppib peptidylprolyl isomerase B gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:19997487 732991 Ppib peptidylprolyl isomerase B gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20151217 MGI PMID:19997487 732991 Ppib peptidylprolyl isomerase B gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0013618 decreased areal bone mineral density IAGP N RGD:5509061 20220915 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0013620 increased internal diameter of femur IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0013626 decreased femur yield load IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20151217 MGI PMID:19997487 732991 Ppib peptidylprolyl isomerase B gene MP:0013633 decreased femur maximal load IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0013638 decreased femur stiffness IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20151217 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20220915 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20151217 MGI PMID:19997487 732991 Ppib peptidylprolyl isomerase B gene MP:0021182 decreased femoral compact bone area IAGP N RGD:5509061 20220915 MGI PMID:24968150 732991 Ppib peptidylprolyl isomerase B gene MP:0021186 decreased bone mineral density of vertebrae IAGP N RGD:5509061 20220915 MGI PMID:24968150 732993 Gabarapl2 GABA type A receptor associated protein like 2 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20201022 MGI 732993 Gabarapl2 GABA type A receptor associated protein like 2 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20190502 MGI 732993 Gabarapl2 GABA type A receptor associated protein like 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 732993 Gabarapl2 GABA type A receptor associated protein like 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 732993 Gabarapl2 GABA type A receptor associated protein like 2 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 732993 Gabarapl2 GABA type A receptor associated protein like 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20201022 MGI 732993 Gabarapl2 GABA type A receptor associated protein like 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21283715 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:20439739 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20439739 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:20439739 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:23479732 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:23479732 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:23479732 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20439739 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:20439739 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:21283715 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:21283715 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:21283715 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21283715 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:21283715 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20439739 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:20439739 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22592798 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23479732 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20439739 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22592798 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:21283715 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21283715 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:21283715 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20439739 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22592798 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22592798 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:20439739 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:22592798 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:22592798 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:22592798 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22592798 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22592798 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22592798 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:22592798 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160804 MGI 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20439739 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21283715 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:21283715 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0020851 abnormal vacuole morphology IAGP N RGD:5509061 20230615 MGI PMID:22308354 732995 Pik3c3 phosphatidylinositol 3-kinase catalytic subunit type 3 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:23479732 732998 Foxq1 forkhead box Q1 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0000411 shiny fur IAGP N RGD:5509061 20141003 MGI PMID:11309849 732998 Foxq1 forkhead box Q1 gene MP:0000411 shiny fur IAGP N RGD:5509061 20141003 MGI PMID:18544931 732998 Foxq1 forkhead box Q1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:18544931 732998 Foxq1 forkhead box Q1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0000505 decreased digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:18544931 732998 Foxq1 forkhead box Q1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:4643821 732998 Foxq1 forkhead box Q1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:4643821 732998 Foxq1 forkhead box Q1 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11309849 732998 Foxq1 forkhead box Q1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:18544931 732998 Foxq1 forkhead box Q1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:4643821 732998 Foxq1 forkhead box Q1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:11309849 732998 Foxq1 forkhead box Q1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:4643821 732998 Foxq1 forkhead box Q1 gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:4643821 732998 Foxq1 forkhead box Q1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:11309849 732998 Foxq1 forkhead box Q1 gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20141003 MGI PMID:11309849 732998 Foxq1 forkhead box Q1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 732998 Foxq1 forkhead box Q1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:4643821 732998 Foxq1 forkhead box Q1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18544931 732998 Foxq1 forkhead box Q1 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:11309849 732998 Foxq1 forkhead box Q1 gene MP:0003811 abnormal hair cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11309849 732998 Foxq1 forkhead box Q1 gene MP:0003812 abnormal hair medulla IAGP N RGD:5509061 20141003 MGI PMID:11309849 732998 Foxq1 forkhead box Q1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:6334024 732998 Foxq1 forkhead box Q1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18544931 732998 Foxq1 forkhead box Q1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16109771 732998 Foxq1 forkhead box Q1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18544931 732998 Foxq1 forkhead box Q1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:4643821 733002 Nherf2 NHERF family PDZ scaffold protein 2 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230720 MGI 733002 Nherf2 NHERF family PDZ scaffold protein 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20230720 MGI 733002 Nherf2 NHERF family PDZ scaffold protein 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20230720 MGI 733002 Nherf2 NHERF family PDZ scaffold protein 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230720 MGI 733002 Nherf2 NHERF family PDZ scaffold protein 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17947234 733002 Nherf2 NHERF family PDZ scaffold protein 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20230720 MGI 733002 Nherf2 NHERF family PDZ scaffold protein 2 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17947234 733004 Abcb9 ATP-binding cassette, sub-family B member 9 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 733004 Abcb9 ATP-binding cassette, sub-family B member 9 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20160811 MGI 733004 Abcb9 ATP-binding cassette, sub-family B member 9 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220519 MGI 733004 Abcb9 ATP-binding cassette, sub-family B member 9 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 733006 Exoc4 exocyst complex component 4 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:9441674 733006 Exoc4 exocyst complex component 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9441674 733006 Exoc4 exocyst complex component 4 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9441674 733006 Exoc4 exocyst complex component 4 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220519 MGI 733006 Exoc4 exocyst complex component 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9441674 733006 Exoc4 exocyst complex component 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733006 Exoc4 exocyst complex component 4 gene MP:0012105 delayed gastrulation IAGP N RGD:5509061 20141003 MGI PMID:9441674 733006 Exoc4 exocyst complex component 4 gene MP:0012131 small visceral yolk sac IAGP N RGD:5509061 20141016 MGI PMID:1653172 733006 Exoc4 exocyst complex component 4 gene MP:0012142 absent amniotic cavity IAGP N RGD:5509061 20141003 MGI PMID:9441674 733006 Exoc4 exocyst complex component 4 gene MP:0012183 decreased paraxial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:9441674 733006 Exoc4 exocyst complex component 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 733006 Exoc4 exocyst complex component 4 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 733009 Dnah10 dynein, axonemal, heavy chain 10 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20211028 MGI PMID:34237282 733009 Dnah10 dynein, axonemal, heavy chain 10 gene MP:0001925 male infertility IAGP N RGD:5509061 20211028 MGI PMID:34237282 733009 Dnah10 dynein, axonemal, heavy chain 10 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20211028 MGI PMID:34237282 733009 Dnah10 dynein, axonemal, heavy chain 10 gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20211028 MGI PMID:34237282 733009 Dnah10 dynein, axonemal, heavy chain 10 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20211028 MGI PMID:34237282 733009 Dnah10 dynein, axonemal, heavy chain 10 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20211028 MGI PMID:34237282 733009 Dnah10 dynein, axonemal, heavy chain 10 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20211028 MGI PMID:34237282 733009 Dnah10 dynein, axonemal, heavy chain 10 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20211028 MGI PMID:34237282 733009 Dnah10 dynein, axonemal, heavy chain 10 gene MP:0014468 disorganized sperm mitochondrial sheath IAGP N RGD:5509061 20240613 MGI PMID:34237282 733009 Dnah10 dynein, axonemal, heavy chain 10 gene MP:0020869 immotile sperm IAGP N RGD:5509061 20211028 MGI PMID:34237282 733011 Blvra biliverdin reductase A gene MP:0000341 abnormal bile color IAGP N RGD:5509061 20221222 MGI PMID:29195835 733011 Blvra biliverdin reductase A gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20170216 MGI PMID:27738106 733011 Blvra biliverdin reductase A gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20221222 MGI PMID:29195835 733011 Blvra biliverdin reductase A gene MP:0002593 high mean erythrocyte cell number IAGP N RGD:5509061 20221222 MGI PMID:29195835 733011 Blvra biliverdin reductase A gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20170216 MGI PMID:27738106 733011 Blvra biliverdin reductase A gene MP:0003674 oxidative stress IAGP N RGD:5509061 20221222 MGI PMID:29195835 733011 Blvra biliverdin reductase A gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20221222 MGI PMID:29195835 733011 Blvra biliverdin reductase A gene MP:0005084 abnormal gallbladder morphology IAGP N RGD:5509061 20221222 MGI PMID:29195835 733011 Blvra biliverdin reductase A gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20170216 MGI PMID:27738106 733011 Blvra biliverdin reductase A gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20170216 MGI PMID:27738106 733011 Blvra biliverdin reductase A gene MP:0005331 insulin resistance IAGP N RGD:5509061 20170216 MGI PMID:27738106 733011 Blvra biliverdin reductase A gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20221222 MGI PMID:29195835 733011 Blvra biliverdin reductase A gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20221222 MGI PMID:29195835 733011 Blvra biliverdin reductase A gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20170216 MGI PMID:27738106 733011 Blvra biliverdin reductase A gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20170216 MGI PMID:27738106 733011 Blvra biliverdin reductase A gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20170216 MGI PMID:27738106 733011 Blvra biliverdin reductase A gene MP:0014174 decreased fatty acid beta-oxidation IAGP N RGD:5509061 20170216 MGI PMID:27738106 733013 Dnase2a deoxyribonuclease II alpha gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:11375492 733013 Dnase2a deoxyribonuclease II alpha gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20170223 MGI PMID:26114879 733013 Dnase2a deoxyribonuclease II alpha gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17066036 733013 Dnase2a deoxyribonuclease II alpha gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170223 MGI PMID:26114879 733013 Dnase2a deoxyribonuclease II alpha gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:12524536 733013 Dnase2a deoxyribonuclease II alpha gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12524536 733013 Dnase2a deoxyribonuclease II alpha gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:12181746 733013 Dnase2a deoxyribonuclease II alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12524536 733013 Dnase2a deoxyribonuclease II alpha gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11375492 733013 Dnase2a deoxyribonuclease II alpha gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12181746 733013 Dnase2a deoxyribonuclease II alpha gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12524536 733013 Dnase2a deoxyribonuclease II alpha gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17066036 733013 Dnase2a deoxyribonuclease II alpha gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12181746 733013 Dnase2a deoxyribonuclease II alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17066036 733013 Dnase2a deoxyribonuclease II alpha gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12524536 733013 Dnase2a deoxyribonuclease II alpha gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12181746 733013 Dnase2a deoxyribonuclease II alpha gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12524536 733013 Dnase2a deoxyribonuclease II alpha gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:17066036 733013 Dnase2a deoxyribonuclease II alpha gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11375492 733013 Dnase2a deoxyribonuclease II alpha gene MP:0002933 joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:17066036 733013 Dnase2a deoxyribonuclease II alpha gene MP:0002933 joint inflammation IAGP N RGD:5509061 20170223 MGI PMID:26114879 733013 Dnase2a deoxyribonuclease II alpha gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20141003 MGI PMID:17066036 733013 Dnase2a deoxyribonuclease II alpha gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20170223 MGI PMID:26114879 733013 Dnase2a deoxyribonuclease II alpha gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20170223 MGI PMID:26114879 733013 Dnase2a deoxyribonuclease II alpha gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:12181746 733013 Dnase2a deoxyribonuclease II alpha gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:17066036 733013 Dnase2a deoxyribonuclease II alpha gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20170223 MGI PMID:26114879 733013 Dnase2a deoxyribonuclease II alpha gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12524536 733013 Dnase2a deoxyribonuclease II alpha gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12524536 733013 Dnase2a deoxyribonuclease II alpha gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:17066036 733013 Dnase2a deoxyribonuclease II alpha gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17066036 733013 Dnase2a deoxyribonuclease II alpha gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20170223 MGI PMID:26114879 733013 Dnase2a deoxyribonuclease II alpha gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20170223 MGI PMID:26114879 733013 Dnase2a deoxyribonuclease II alpha gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:17066036 733013 Dnase2a deoxyribonuclease II alpha gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:17066036 733013 Dnase2a deoxyribonuclease II alpha gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11375492 733013 Dnase2a deoxyribonuclease II alpha gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12524536 733013 Dnase2a deoxyribonuclease II alpha gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17066036 733013 Dnase2a deoxyribonuclease II alpha gene MP:0009851 abnormal Sertoli cell phagocytosis IAGP N RGD:5509061 20240404 MGI PMID:31712393 733013 Dnase2a deoxyribonuclease II alpha gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12181746 733013 Dnase2a deoxyribonuclease II alpha gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11375492 733018 Calu calumenin gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20210128 MGI 733018 Calu calumenin gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20210128 MGI 733018 Calu calumenin gene MP:0000897 abnormal midbrain morphology IEA N RGD:5509061 20210128 MGI 733018 Calu calumenin gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210128 MGI 733018 Calu calumenin gene MP:0002217 small lymph nodes IEA N RGD:5509061 20220519 MGI 733018 Calu calumenin gene MP:0003257 abnormal abdominal wall morphology IEA N RGD:5509061 20210128 MGI 733018 Calu calumenin gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 733018 Calu calumenin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 733022 Gzmb granzyme B gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:15699143 733022 Gzmb granzyme B gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16618603 733022 Gzmb granzyme B gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:9362539 733022 Gzmb granzyme B gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:17919943 733022 Gzmb granzyme B gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:12594834 733022 Gzmb granzyme B gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:16116214 733022 Gzmb granzyme B gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16618603 733022 Gzmb granzyme B gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:15699143 733022 Gzmb granzyme B gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:8137431 733022 Gzmb granzyme B gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16618603 733022 Gzmb granzyme B gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17919943 733022 Gzmb granzyme B gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15061770 733022 Gzmb granzyme B gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17919943 733022 Gzmb granzyme B gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17919943 733022 Gzmb granzyme B gene MP:0012191 decreased cytotoxic T cell apoptosis IAGP N RGD:5509061 20180118 MGI PMID:22801574 733022 Gzmb granzyme B gene MP:0020943 increased susceptibility to Flaviviridae infection IAGP N RGD:5509061 20200430 MGI PMID:15061770 733028 Pmpcb peptidase (mitochondrial processing) beta gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20111116 MGI 733028 Pmpcb peptidase (mitochondrial processing) beta gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20241024 MGI PMID:32376682 733028 Pmpcb peptidase (mitochondrial processing) beta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733028 Pmpcb peptidase (mitochondrial processing) beta gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23190530 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:23190530 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0000256 echinocytosis IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0000314 schistocytosis IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:23190530 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23190530 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23190530 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19882669 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23190530 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23190530 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19882669 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:23190530 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23190530 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19882669 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19882669 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0004266 pale placenta IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:23190530 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19882669 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20161774 733033 Slc20a1 solute carrier family 20, member 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20161774 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0000088 short mandible IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0000111 cleft palate IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0000114 cleft chin IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0000274 enlarged heart IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0001730 embryonic growth arrest IEA N RGD:5509061 20240926 MGI 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20240523 MGI 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0003872 absent heart right ventricle IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0005380 embryo phenotype IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0005385 cardiovascular system phenotype IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0008797 facial cleft IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0009781 abnormal preimplantation embryo development IEA N RGD:5509061 20240801 MGI 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0010428 abnormal heart right ventricle outflow tract morphology IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20191128 MGI 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0012129 failure of blastocyst formation IEA N RGD:5509061 20191128 MGI 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0012492 pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0030047 flat forehead IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0030122 temporal bone squamous part hypoplasia IAGP N RGD:5509061 20230928 MGI PMID:37075751 733035 Polr1a polymerase (RNA) I polypeptide A gene MP:0031445 midline cleft upper lip IAGP N RGD:5509061 20231102 MGI PMID:37075751 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20201210 MGI PMID:21277849 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20201210 MGI PMID:21277849 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20141003 MGI PMID:21045126 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21045126 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20201210 MGI PMID:21277849 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20201210 MGI PMID:21277849 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20201210 MGI PMID:21277849 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20201210 MGI PMID:21277849 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20201210 MGI PMID:21277849 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:21045126 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20201210 MGI PMID:21277849 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0008670 decreased interleukin-12b secretion IAGP N RGD:5509061 20201210 MGI PMID:21277849 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0008676 decreased interleukin-15 secretion IAGP N RGD:5509061 20201210 MGI PMID:21277849 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0008685 decreased interleukin-18 secretion IAGP N RGD:5509061 20201210 MGI PMID:21277849 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21045126 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20201210 MGI PMID:21277849 733039 Slc15a4 solute carrier family 15, member 4 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20201210 MGI PMID:21277849 733040 Cldn16 claudin 16 gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:20147368 733040 Cldn16 claudin 16 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:20147368 733040 Cldn16 claudin 16 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:20147368 733040 Cldn16 claudin 16 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:20147368 733040 Cldn16 claudin 16 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:20147368 733040 Cldn16 claudin 16 gene MP:0010111 abnormal renal calcium reabsorption IAGP N RGD:5509061 20141003 MGI PMID:20147368 733040 Cldn16 claudin 16 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:20147368 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:16571627 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:16116426 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12421720 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:12421720 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:12421720 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12421720 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:12421720 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16571627 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0001446 abnormal whisker trimming behavior IAGP N RGD:5509061 20141003 MGI PMID:9298901 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:9298901 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:9298901 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:16571627 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:12421720 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16571627 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16571627 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:9298901 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:12421720 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0002635 reduced sensorimotor gating IAGP N RGD:5509061 20141003 MGI PMID:9298901 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:16571627 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:12421720 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16571627 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0004407 increased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16116426 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16116426 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16571627 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:16571627 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:9298901 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16571627 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16571627 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12421720 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19008950 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0012675 enlarged floor plate IAGP N RGD:5509061 20141003 MGI PMID:16571627 733043 Dvl1 dishevelled segment polarity protein 1 gene MP:0021117 abnormal huddling behavior IAGP N RGD:5509061 20220519 MGI PMID:9298901 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:18818193 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20582225 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20181129 MGI PMID:25852647 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20181129 MGI PMID:25852647 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20181129 MGI PMID:25852647 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20181129 MGI PMID:25852647 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:18818193 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000440 domed cranium IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000440 domed cranium IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000445 short snout IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21504907 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000548 long limbs IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000566 synostosis IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:20582225 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001184 absent pulmonary alveoli IAGP N RGD:5509061 20141003 MGI PMID:9716527 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20530870 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9716527 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:9716527 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9716527 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:9716527 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:9716527 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:21504907 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21504907 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9716527 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17117437 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002758 long tail IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002758 long tail IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002758 long tail IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002764 short tibia IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003109 short femur IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003109 short femur IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003151 absent tunnel of Corti IAGP N RGD:5509061 20141003 MGI PMID:17117437 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003151 absent tunnel of Corti IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003152 abnormal pillar cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17117437 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003152 abnormal pillar cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9716527 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17117437 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003417 premature endochondral bone ossification IAGP N RGD:5509061 20171221 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18818193 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003840 abnormal coronal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003841 abnormal lambdoid suture morphology IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004053 abnormal synchondrosis IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20181129 MGI PMID:25852647 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004302 abnormal Deiters cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18818193 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004302 abnormal Deiters cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004312 absent pillar cells IAGP N RGD:5509061 20141003 MGI PMID:17117437 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004312 absent pillar cells IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004348 long femur IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004348 long femur IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004348 long femur IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004348 long femur IAGP N RGD:5509061 20141003 MGI PMID:20582225 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004348 long femur IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004348 long femur IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004350 long humerus IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004350 long humerus IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004350 long humerus IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004357 long tibia IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004361 bowed ulna IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004370 long ulna IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004370 long ulna IAGP N RGD:5509061 20141003 MGI PMID:17360456 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004371 bowed femur IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004371 bowed femur IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004371 bowed femur IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004371 bowed femur IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004372 bowed fibula IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004372 bowed fibula IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004373 bowed humerus IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004380 short frontal bone IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004386 enlarged interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18818193 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:17117437 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004441 small occipital bone IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004471 short nasal bone IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004537 abnormal palatine bone horizontal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004626 vertebral compression IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004632 abnormal cochlear OHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004652 small caudal vertebrae IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004669 enlarged vertebral body IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004705 elongated vertebral body IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004706 short vertebral body IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004706 short vertebral body IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004708 short lumbar vertebrae IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:17117437 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004831 long incisors IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004831 long incisors IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004840 increased Deiters cell number IAGP N RGD:5509061 20141003 MGI PMID:17117437 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004840 increased Deiters cell number IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0005269 abnormal occipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:9716527 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:18818193 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006331 abnormal patterning of the organ of Corti IAGP N RGD:5509061 20141003 MGI PMID:18818193 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006394 abnormal vertebral epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:20530870 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:9887329 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20141003 MGI PMID:22367969 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006429 abnormal hyaline cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006432 abnormal costal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0006432 abnormal costal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21504907 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008278 failure of sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008304 abnormal organ of Corti supporting cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18818193 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0008951 long radius IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20582225 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0009911 increased hyoid bone size IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010208 prognathia IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010208 prognathia IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010208 prognathia IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010282 decreased organ/body region tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23867472 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20181129 MGI PMID:25852647 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010941 abnormal foramen magnum morphology IAGP N RGD:5509061 20141003 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010941 abnormal foramen magnum morphology IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010941 abnormal foramen magnum morphology IAGP N RGD:5509061 20141003 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010941 abnormal foramen magnum morphology IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010964 increased compact bone volume IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0010970 abnormal compact bone lamellar structure IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14751559 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011496 abnormal head size IAGP N RGD:5509061 20141003 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17117437 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18818193 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:8630492 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20171123 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0012279 wide sternum IAGP N RGD:5509061 20141003 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0012556 increased cell death IAGP N RGD:5509061 20180301 MGI PMID:28483978 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0012683 absent telencephalon IAGP N RGD:5509061 20180301 MGI PMID:28483978 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0013176 abnormal tail position or orientation IEA N RGD:5509061 20141003 MGI 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0013179 wavy tail IAGP N RGD:5509061 20141003 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20220915 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0013626 decreased femur yield load IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0013633 decreased femur maximal load IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0013639 decreased bone stiffness IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0013642 decreased vertebra stiffness IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0013643 decreased vertebra maximal load IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0013646 decreased energy dissipated prior to femur fracture IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0014099 abnormal chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0014100 increased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0014288 rhizomelic limb IAGP N RGD:5509061 20230824 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:8601314 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0021135 abnormal annulus fibrosus morphology IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0021186 decreased bone mineral density of vertebrae IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030094 foramen magnum stenosis IAGP N RGD:5509061 20170928 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030190 small snout IAGP N RGD:5509061 20171019 MGI PMID:23200862 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030245 round head IAGP N RGD:5509061 20171019 MGI PMID:10861287 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030245 round head IAGP N RGD:5509061 20171019 MGI PMID:11406607 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030245 round head IAGP N RGD:5509061 20180118 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030245 round head IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030274 maxillary retrognathia IAGP N RGD:5509061 20171026 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030275 thin frontal bone IAGP N RGD:5509061 20171102 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030281 thin parietal bone IAGP N RGD:5509061 20171102 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030302 abnormal maxillary zygomatic process morphology IAGP N RGD:5509061 20171102 MGI PMID:19086028 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030367 premature metopic suture closure IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030370 absent jugum limitans IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030383 small presphenoid bone IAGP N RGD:5509061 20171214 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030420 short basicranium IAGP N RGD:5509061 20171214 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030420 short basicranium IAGP N RGD:5509061 20171214 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030420 short basicranium IAGP N RGD:5509061 20171214 MGI PMID:19073250 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030420 short basicranium IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030435 premature craniofacial suture closure IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030444 premature cranial synchondrosis closure IAGP N RGD:5509061 20171214 MGI PMID:11181569 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030444 premature cranial synchondrosis closure IAGP N RGD:5509061 20180111 MGI PMID:10587515 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030444 premature cranial synchondrosis closure IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030446 premature sphenooccipital synchondrosis closure IAGP N RGD:5509061 20230824 MGI PMID:37345656 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20180125 MGI PMID:10200283 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030541 misaligned incisors IAGP N RGD:5509061 20200528 MGI PMID:28230213 733045 Fgfr3 fibroblast growth factor receptor 3 gene MP:0030792 large femur head IAGP N RGD:5509061 20181011 MGI PMID:8601314 733046 Prop1 paired like homeodomain factor 1 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:16556738 733046 Prop1 paired like homeodomain factor 1 gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:14173795 733046 Prop1 paired like homeodomain factor 1 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20210729 MGI PMID:31987917 733046 Prop1 paired like homeodomain factor 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:14173795 733046 Prop1 paired like homeodomain factor 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16556738 733046 Prop1 paired like homeodomain factor 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8934515 733046 Prop1 paired like homeodomain factor 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8934515 733046 Prop1 paired like homeodomain factor 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0002659 pituitary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0002659 pituitary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16556738 733046 Prop1 paired like homeodomain factor 1 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:590190 733046 Prop1 paired like homeodomain factor 1 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:14173795 733046 Prop1 paired like homeodomain factor 1 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0003348 hypopituitarism IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141003 MGI PMID:16556738 733046 Prop1 paired like homeodomain factor 1 gene MP:0003972 decreased pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:12183375 733046 Prop1 paired like homeodomain factor 1 gene MP:0004164 abnormal neurohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0005119 decreased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:7390396 733046 Prop1 paired like homeodomain factor 1 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:7390396 733046 Prop1 paired like homeodomain factor 1 gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:590190 733046 Prop1 paired like homeodomain factor 1 gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:590190 733046 Prop1 paired like homeodomain factor 1 gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:590190 733046 Prop1 paired like homeodomain factor 1 gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12183375 733046 Prop1 paired like homeodomain factor 1 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:12183375 733046 Prop1 paired like homeodomain factor 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:12742526 733046 Prop1 paired like homeodomain factor 1 gene MP:0008320 absent adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:12183375 733046 Prop1 paired like homeodomain factor 1 gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:14173795 733046 Prop1 paired like homeodomain factor 1 gene MP:0008330 absent somatotrophs IAGP N RGD:5509061 20141003 MGI PMID:6194978 733046 Prop1 paired like homeodomain factor 1 gene MP:0008336 absent gonadotrophs IAGP N RGD:5509061 20141003 MGI PMID:12183375 733046 Prop1 paired like homeodomain factor 1 gene MP:0008338 decreased thyrotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:14173795 733046 Prop1 paired like homeodomain factor 1 gene MP:0008365 adenohypophysis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20210729 MGI PMID:31987917 733046 Prop1 paired like homeodomain factor 1 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:8934515 733046 Prop1 paired like homeodomain factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15459176 733046 Prop1 paired like homeodomain factor 1 gene MP:0011120 increased primordial ovarian follicle number IAGP N RGD:5509061 20210729 MGI PMID:31987917 733046 Prop1 paired like homeodomain factor 1 gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:31987917 733046 Prop1 paired like homeodomain factor 1 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20210729 MGI PMID:31987917 733046 Prop1 paired like homeodomain factor 1 gene MP:0011130 absent tertiary ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:14173795 733046 Prop1 paired like homeodomain factor 1 gene MP:0013337 abnormal adenohypophysis development IAGP N RGD:5509061 20141211 MGI PMID:16678101 733046 Prop1 paired like homeodomain factor 1 gene MP:0013349 small Rathke's pouch IAGP N RGD:5509061 20141218 MGI PMID:12183375 733046 Prop1 paired like homeodomain factor 1 gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:12183375 733046 Prop1 paired like homeodomain factor 1 gene MP:0013352 abnormal Rathke's pouch apoptosis IAGP N RGD:5509061 20141218 MGI PMID:12183375 733046 Prop1 paired like homeodomain factor 1 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:31987917 733048 Plk2 polo like kinase 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12972611 733048 Plk2 polo like kinase 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12972611 733048 Plk2 polo like kinase 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:12972611 733048 Plk2 polo like kinase 2 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:12972611 733048 Plk2 polo like kinase 2 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:12972611 733048 Plk2 polo like kinase 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:12972611 733048 Plk2 polo like kinase 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:12972611 733048 Plk2 polo like kinase 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12972611 733048 Plk2 polo like kinase 2 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:12972611 733048 Plk2 polo like kinase 2 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:12972611 733048 Plk2 polo like kinase 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19004816 733052 Tnnt1 troponin T1, skeletal, slow gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20151217 MGI PMID:24445317 733052 Tnnt1 troponin T1, skeletal, slow gene MP:0004036 abnormal muscle relaxation IAGP N RGD:5509061 20151217 MGI PMID:24445317 733052 Tnnt1 troponin T1, skeletal, slow gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20151217 MGI PMID:24445317 733052 Tnnt1 troponin T1, skeletal, slow gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20151217 MGI PMID:24445317 733052 Tnnt1 troponin T1, skeletal, slow gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20151217 MGI PMID:24445317 733052 Tnnt1 troponin T1, skeletal, slow gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20151217 MGI PMID:24445317 733052 Tnnt1 troponin T1, skeletal, slow gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20151217 MGI PMID:24445317 733052 Tnnt1 troponin T1, skeletal, slow gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20151217 MGI PMID:24445317 733052 Tnnt1 troponin T1, skeletal, slow gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20151217 MGI PMID:24445317 733052 Tnnt1 troponin T1, skeletal, slow gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20151217 MGI PMID:24445317 733052 Tnnt1 troponin T1, skeletal, slow gene MP:0009458 abnormal skeletal muscle size IAGP N RGD:5509061 20151217 MGI PMID:24445317 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:19734217 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:15254596 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20713880 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23338236 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:19734217 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0003426 pulmonary interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15254596 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:15718500 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:16941672 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15718500 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:11085753 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:19734217 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:19734217 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20111116 MGI 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:19734217 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:15254596 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:15152045 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:15718500 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:15152045 733057 Cxcr3 C-X-C motif chemokine receptor 3 gene MP:0031023 decreased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:15152045 733059 Aspa aspartoacylase gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:14572139 733059 Aspa aspartoacylase gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:10894262 733059 Aspa aspartoacylase gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:14572139 733059 Aspa aspartoacylase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10894262 733059 Aspa aspartoacylase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12955145 733059 Aspa aspartoacylase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:18987190 733059 Aspa aspartoacylase gene MP:0000745 tremors IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0000745 tremors IAGP N RGD:5509061 20160811 MGI PMID:24682784 733059 Aspa aspartoacylase gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:21625469 733059 Aspa aspartoacylase gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:21625469 733059 Aspa aspartoacylase gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10894262 733059 Aspa aspartoacylase gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:18987190 733059 Aspa aspartoacylase gene MP:0000921 demyelination IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18987190 733059 Aspa aspartoacylase gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:14572139 733059 Aspa aspartoacylase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10894262 733059 Aspa aspartoacylase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14572139 733059 Aspa aspartoacylase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21625469 733059 Aspa aspartoacylase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12955145 733059 Aspa aspartoacylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18987190 733059 Aspa aspartoacylase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21625469 733059 Aspa aspartoacylase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20211021 MGI 733059 Aspa aspartoacylase gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20170105 MGI 733059 Aspa aspartoacylase gene MP:0001314 cornea opacity IEA N RGD:5509061 20170105 MGI 733059 Aspa aspartoacylase gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21625469 733059 Aspa aspartoacylase gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10894262 733059 Aspa aspartoacylase gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18987190 733059 Aspa aspartoacylase gene MP:0001393 ataxia IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0001393 ataxia IAGP N RGD:5509061 20160811 MGI PMID:24682784 733059 Aspa aspartoacylase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160811 MGI PMID:24682784 733059 Aspa aspartoacylase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12955145 733059 Aspa aspartoacylase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18987190 733059 Aspa aspartoacylase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21625469 733059 Aspa aspartoacylase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18987190 733059 Aspa aspartoacylase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21625469 733059 Aspa aspartoacylase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160811 MGI PMID:24682784 733059 Aspa aspartoacylase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20240704 MGI PMID:38282243 733059 Aspa aspartoacylase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10894262 733059 Aspa aspartoacylase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18987190 733059 Aspa aspartoacylase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21625469 733059 Aspa aspartoacylase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 733059 Aspa aspartoacylase gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20160811 MGI PMID:24682784 733059 Aspa aspartoacylase gene MP:0001513 limb grasping IEA N RGD:5509061 20170105 MGI 733059 Aspa aspartoacylase gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:10894262 733059 Aspa aspartoacylase gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:18987190 733059 Aspa aspartoacylase gene MP:0002064 seizures IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10894262 733059 Aspa aspartoacylase gene MP:0002083 premature death IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20240704 MGI PMID:38282243 733059 Aspa aspartoacylase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21625469 733059 Aspa aspartoacylase gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:21625469 733059 Aspa aspartoacylase gene MP:0002204 abnormal synaptic neurotransmitter level IAGP N RGD:5509061 20141003 MGI PMID:14572139 733059 Aspa aspartoacylase gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20170105 MGI 733059 Aspa aspartoacylase gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:10894262 733059 Aspa aspartoacylase gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:18987190 733059 Aspa aspartoacylase gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:21625469 733059 Aspa aspartoacylase gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20160811 MGI PMID:24682784 733059 Aspa aspartoacylase gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 733059 Aspa aspartoacylase gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:18987190 733059 Aspa aspartoacylase gene MP:0003354 astrocytosis IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20240704 MGI PMID:38282243 733059 Aspa aspartoacylase gene MP:0004142 abnormal muscle tone IAGP N RGD:5509061 20141003 MGI PMID:21625469 733059 Aspa aspartoacylase gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:21625469 733059 Aspa aspartoacylase gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:10894262 733059 Aspa aspartoacylase gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:12955145 733059 Aspa aspartoacylase gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10894262 733059 Aspa aspartoacylase gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:10894262 733059 Aspa aspartoacylase gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:18987190 733059 Aspa aspartoacylase gene MP:0005405 axon degeneration IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:21625469 733059 Aspa aspartoacylase gene MP:0006303 abnormal retina nerve fiber layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10894262 733059 Aspa aspartoacylase gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:18987190 733059 Aspa aspartoacylase gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20160811 MGI PMID:24682784 733059 Aspa aspartoacylase gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20240704 MGI PMID:38282243 733059 Aspa aspartoacylase gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:18987190 733059 Aspa aspartoacylase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20170105 MGI 733059 Aspa aspartoacylase gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:18987190 733059 Aspa aspartoacylase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:14572139 733059 Aspa aspartoacylase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20170105 MGI 733059 Aspa aspartoacylase gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:14572139 733059 Aspa aspartoacylase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10894262 733059 Aspa aspartoacylase gene MP:0011940 decreased food intake IEA N RGD:5509061 20210128 MGI 733059 Aspa aspartoacylase gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20160811 MGI PMID:24682784 733059 Aspa aspartoacylase gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20160811 MGI PMID:24682784 733059 Aspa aspartoacylase gene MP:0012230 abnormal sphingolipid level IAGP N RGD:5509061 20160609 MGI PMID:26511242 733059 Aspa aspartoacylase gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20170105 MGI 733059 Aspa aspartoacylase gene MP:0021190 decreased bone mineral density of lumbar vertebrae IAGP N RGD:5509061 20220922 MGI PMID:14572139 733059 Aspa aspartoacylase gene MP:0030733 decreased gamma-aminobutyric acid level IAGP N RGD:5509061 20180927 MGI PMID:14572139 733059 Aspa aspartoacylase gene MP:0030737 decreased glutamic acid level IAGP N RGD:5509061 20180927 MGI PMID:14572139 733059 Aspa aspartoacylase gene MP:0030742 increased aspartic acid level IAGP N RGD:5509061 20180927 MGI PMID:14572139 733060 Tmem33 transmembrane protein 33 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 733060 Tmem33 transmembrane protein 33 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20211021 MGI 733062 Bad BCL2-associated agonist of cell death gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18223655 733062 Bad BCL2-associated agonist of cell death gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12431371 733062 Bad BCL2-associated agonist of cell death gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12876200 733062 Bad BCL2-associated agonist of cell death gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:16780816 733062 Bad BCL2-associated agonist of cell death gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12876200 733062 Bad BCL2-associated agonist of cell death gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:18223655 733062 Bad BCL2-associated agonist of cell death gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20211216 MGI PMID:25985365 733062 Bad BCL2-associated agonist of cell death gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12431371 733062 Bad BCL2-associated agonist of cell death gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12876200 733062 Bad BCL2-associated agonist of cell death gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12431371 733062 Bad BCL2-associated agonist of cell death gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:12876200 733062 Bad BCL2-associated agonist of cell death gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12876200 733062 Bad BCL2-associated agonist of cell death gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12876200 733062 Bad BCL2-associated agonist of cell death gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18223655 733062 Bad BCL2-associated agonist of cell death gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12876200 733062 Bad BCL2-associated agonist of cell death gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12431371 733062 Bad BCL2-associated agonist of cell death gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12431371 733062 Bad BCL2-associated agonist of cell death gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12876200 733062 Bad BCL2-associated agonist of cell death gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:16780816 733062 Bad BCL2-associated agonist of cell death gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12876200 733062 Bad BCL2-associated agonist of cell death gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12876200 733062 Bad BCL2-associated agonist of cell death gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18223655 733062 Bad BCL2-associated agonist of cell death gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:18223655 733062 Bad BCL2-associated agonist of cell death gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18223655 733062 Bad BCL2-associated agonist of cell death gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:12431371 733062 Bad BCL2-associated agonist of cell death gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18223655 733062 Bad BCL2-associated agonist of cell death gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18223655 733062 Bad BCL2-associated agonist of cell death gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12431371 733062 Bad BCL2-associated agonist of cell death gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12431371 733062 Bad BCL2-associated agonist of cell death gene MP:0009167 increased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:18223655 733062 Bad BCL2-associated agonist of cell death gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:18223655 733062 Bad BCL2-associated agonist of cell death gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12876200 733062 Bad BCL2-associated agonist of cell death gene MP:0014117 increased pancreatic beta cell apoptosis IAGP N RGD:5509061 20180614 MGI PMID:18223655 733062 Bad BCL2-associated agonist of cell death gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:12876200 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20200402 MGI 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:11517255 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11517255 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11517255 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11517255 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11517255 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11517255 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220428 MGI 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11517255 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:11517255 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11517255 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11517255 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:11517255 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:11517255 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11517255 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:11517255 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20200402 MGI 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11517255 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20211021 MGI 733064 Kcnc3 potassium voltage gated channel, Shaw-related subfamily, member 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:11517255 733066 Fgf16 fibroblast growth factor 16 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18565327 733066 Fgf16 fibroblast growth factor 16 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18565327 733066 Fgf16 fibroblast growth factor 16 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18565327 733066 Fgf16 fibroblast growth factor 16 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18565327 733066 Fgf16 fibroblast growth factor 16 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18816849 733066 Fgf16 fibroblast growth factor 16 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:18816849 733066 Fgf16 fibroblast growth factor 16 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:18565327 733066 Fgf16 fibroblast growth factor 16 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18816849 733066 Fgf16 fibroblast growth factor 16 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18816849 733066 Fgf16 fibroblast growth factor 16 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18565327 733066 Fgf16 fibroblast growth factor 16 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18565327 733066 Fgf16 fibroblast growth factor 16 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:18565327 733066 Fgf16 fibroblast growth factor 16 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:18565327 733066 Fgf16 fibroblast growth factor 16 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18565327 733066 Fgf16 fibroblast growth factor 16 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18565327 733067 Ddit4 DNA-damage-inducible transcript 4 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15988001 733067 Ddit4 DNA-damage-inducible transcript 4 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15452091 733067 Ddit4 DNA-damage-inducible transcript 4 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141003 MGI PMID:24048858 733067 Ddit4 DNA-damage-inducible transcript 4 gene MP:0030006 decreased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:15452091 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9039266 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20180111 MGI PMID:11087268 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10555147 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9039266 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:14966518 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:9039266 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:9618528 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20180111 MGI PMID:11087268 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:14966518 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:9039266 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:9618528 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20180111 MGI PMID:11087268 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:9039266 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20230803 MGI PMID:30048712 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20230803 MGI PMID:30048712 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20230803 MGI PMID:30048712 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20180111 MGI PMID:11087268 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:18713466 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14966518 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20180111 MGI PMID:11087268 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:10555147 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9039266 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9618528 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:10555147 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9039266 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9618528 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141003 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20180111 MGI PMID:11087268 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:18713466 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20230803 MGI PMID:30048712 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9039266 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20180111 MGI PMID:11087268 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20190704 MGI PMID:9039266 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:20044516 733069 Csrp3 cysteine and glycine-rich protein 3 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:30048712 733071 Fcna ficolin A gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23150716 733071 Fcna ficolin A gene MP:0009062 impaired lectin complement pathway IAGP N RGD:5509061 20141003 MGI PMID:23150716 733071 Fcna ficolin A gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23150716 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20190502 MGI 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:15342464 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17289807 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20160421 MGI 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17289807 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17289807 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17289807 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17289807 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:17289807 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0002872 polycythemia IAGP N RGD:5509061 20141003 MGI PMID:15084469 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:17289807 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:15342464 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:17289807 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0003998 decreased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:15084469 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:17289807 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0005638 hemochromatosis IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:15084469 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0008737 abnormal spleen physiology IAGP N RGD:5509061 20141003 MGI PMID:15342464 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0008738 abnormal liver iron level IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:15342464 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:15084469 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:17289807 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:15342464 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0009322 increased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15342464 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0009323 abnormal spleen development IAGP N RGD:5509061 20141003 MGI PMID:15342464 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160421 MGI 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0010175 leptocytosis IAGP N RGD:5509061 20141003 MGI PMID:17289807 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17289807 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IEA N RGD:5509061 20141003 MGI 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0011106 embryonic lethality between implantation and somite formation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0011886 increased circulating lipase level IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20141003 MGI PMID:17289807 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0011896 increased circulating unsaturated transferrin level IAGP N RGD:5509061 20141003 MGI PMID:17289807 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0011897 decreased circulating unsaturated transferrin level IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0013302 increased pancreas iron level IAGP N RGD:5509061 20150101 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0020365 increased brain iron level IAGP N RGD:5509061 20161020 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0020367 increased heart iron level IAGP N RGD:5509061 20161020 MGI PMID:25100063 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0020369 increased intestinal iron level IAGP N RGD:5509061 20161020 MGI PMID:16054062 733073 Slc40a1 solute carrier family 40 (iron-regulated transporter), member 1 gene MP:0020385 decreased intestinal iron level IAGP N RGD:5509061 20161020 MGI PMID:25100063 733078 Oplah 5-oxoprolinase (ATP-hydrolysing) gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 733078 Oplah 5-oxoprolinase (ATP-hydrolysing) gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 733078 Oplah 5-oxoprolinase (ATP-hydrolysing) gene MP:0001488 increased startle reflex IEA N RGD:5509061 20160421 MGI 733078 Oplah 5-oxoprolinase (ATP-hydrolysing) gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210520 MGI 733078 Oplah 5-oxoprolinase (ATP-hydrolysing) gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 733078 Oplah 5-oxoprolinase (ATP-hydrolysing) gene MP:0011897 decreased circulating unsaturated transferrin level IEA N RGD:5509061 20211021 MGI 733079 Tmem176b transmembrane protein 176B gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:16814752 733079 Tmem176b transmembrane protein 176B gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:16814752 733079 Tmem176b transmembrane protein 176B gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:16814752 733079 Tmem176b transmembrane protein 176B gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16814752 733079 Tmem176b transmembrane protein 176B gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:16814752 733079 Tmem176b transmembrane protein 176B gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16814752 733079 Tmem176b transmembrane protein 176B gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16814752 733080 Ap2a2 adaptor-related protein complex 2, alpha 2 subunit gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20160421 MGI 733080 Ap2a2 adaptor-related protein complex 2, alpha 2 subunit gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20210128 MGI 733080 Ap2a2 adaptor-related protein complex 2, alpha 2 subunit gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20160421 MGI 733080 Ap2a2 adaptor-related protein complex 2, alpha 2 subunit gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 733080 Ap2a2 adaptor-related protein complex 2, alpha 2 subunit gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20160421 MGI 733080 Ap2a2 adaptor-related protein complex 2, alpha 2 subunit gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 733080 Ap2a2 adaptor-related protein complex 2, alpha 2 subunit gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 733080 Ap2a2 adaptor-related protein complex 2, alpha 2 subunit gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20170105 MGI 733080 Ap2a2 adaptor-related protein complex 2, alpha 2 subunit gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 733080 Ap2a2 adaptor-related protein complex 2, alpha 2 subunit gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 733080 Ap2a2 adaptor-related protein complex 2, alpha 2 subunit gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 733083 Gpr83 G protein-coupled receptor 83 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 733083 Gpr83 G protein-coupled receptor 83 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 733083 Gpr83 G protein-coupled receptor 83 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 733083 Gpr83 G protein-coupled receptor 83 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18479351 733083 Gpr83 G protein-coupled receptor 83 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 733083 Gpr83 G protein-coupled receptor 83 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 733083 Gpr83 G protein-coupled receptor 83 gene MP:0001262 decreased body weight IEA N RGD:5509061 20230601 MGI 733083 Gpr83 G protein-coupled receptor 83 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23088626 733083 Gpr83 G protein-coupled receptor 83 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23088626 733083 Gpr83 G protein-coupled receptor 83 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230601 MGI 733083 Gpr83 G protein-coupled receptor 83 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17893329 733083 Gpr83 G protein-coupled receptor 83 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20230601 MGI 733083 Gpr83 G protein-coupled receptor 83 gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20230601 MGI 733083 Gpr83 G protein-coupled receptor 83 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18479351 733083 Gpr83 G protein-coupled receptor 83 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 733083 Gpr83 G protein-coupled receptor 83 gene MP:0011976 sweet preference IAGP N RGD:5509061 20141003 MGI PMID:23088626 733083 Gpr83 G protein-coupled receptor 83 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20141003 MGI PMID:23088626 733083 Gpr83 G protein-coupled receptor 83 gene MP:0013519 decreased CD4-positive NK T cell number IEA N RGD:5509061 20230601 MGI 733083 Gpr83 G protein-coupled receptor 83 gene MP:0013522 decreased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20230601 MGI 733086 Cetn3 centrin 3 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20191114 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20191114 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20191114 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20191114 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20191114 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20191114 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20191114 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20191114 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20191114 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20191114 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20191114 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20191114 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20191114 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20191114 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0020814 abnormal photoreceptor outer segment diameter IAGP N RGD:5509061 20191114 MGI PMID:30647131 733086 Cetn3 centrin 3 gene MP:0030988 dysosmia IAGP N RGD:5509061 20200102 MGI PMID:30647131 733088 Cap1 cyclase associated actin cytoskeleton regulatory protein 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20230323 MGI PMID:33845164 733088 Cap1 cyclase associated actin cytoskeleton regulatory protein 1 gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20230323 MGI PMID:33845164 733088 Cap1 cyclase associated actin cytoskeleton regulatory protein 1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20230323 MGI PMID:33845164 733088 Cap1 cyclase associated actin cytoskeleton regulatory protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20230323 MGI PMID:33845164 733088 Cap1 cyclase associated actin cytoskeleton regulatory protein 1 gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20230323 MGI PMID:33845164 733096 Hmbs hydroxymethylbilane synthase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0000745 tremors IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0001258 decreased body length IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0001265 decreased body size IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 733096 Hmbs hydroxymethylbilane synthase gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:8563760 733096 Hmbs hydroxymethylbilane synthase gene MP:0001393 ataxia IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 733096 Hmbs hydroxymethylbilane synthase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:8563760 733096 Hmbs hydroxymethylbilane synthase gene MP:0001488 increased startle reflex IEA N RGD:5509061 20181227 MGI 733096 Hmbs hydroxymethylbilane synthase gene MP:0001513 limb grasping IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0002083 premature death IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8563760 733096 Hmbs hydroxymethylbilane synthase gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20181227 MGI 733096 Hmbs hydroxymethylbilane synthase gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:8563760 733096 Hmbs hydroxymethylbilane synthase gene MP:0005150 cachexia IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:8563760 733096 Hmbs hydroxymethylbilane synthase gene MP:0005424 jerky movement IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0005654 porphyria IAGP N RGD:5509061 20141003 MGI PMID:8563760 733096 Hmbs hydroxymethylbilane synthase gene MP:0005654 porphyria IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:8563760 733096 Hmbs hydroxymethylbilane synthase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8563760 733096 Hmbs hydroxymethylbilane synthase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8563760 733096 Hmbs hydroxymethylbilane synthase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733096 Hmbs hydroxymethylbilane synthase gene MP:0011188 increased erythrocyte protoporphyrin level IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0011414 erythruria IAGP N RGD:5509061 20141003 MGI PMID:8563760 733096 Hmbs hydroxymethylbilane synthase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 733096 Hmbs hydroxymethylbilane synthase gene MP:0020284 decreased hydroxymethylbilane synthase level IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0020456 decreased myelin sheath amount IAGP N RGD:5509061 20200402 MGI PMID:30615115 733096 Hmbs hydroxymethylbilane synthase gene MP:0031496 motor developmental delay IAGP N RGD:5509061 20230810 MGI PMID:30615115 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20190815 MGI PMID:21515572 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0000287 heart valve hypoplasia IAGP N RGD:5509061 20190822 MGI PMID:31232685 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20190815 MGI PMID:21515572 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20190822 MGI PMID:31232685 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0001785 edema IAGP N RGD:5509061 20190822 MGI PMID:31232685 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20190822 MGI PMID:31232685 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20190815 MGI PMID:21515572 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20190822 MGI PMID:31232685 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0009902 abnormal lateral nasal prominence morphology IAGP N RGD:5509061 20190822 MGI PMID:31232685 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20190822 MGI PMID:31232685 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0010500 myocardium hypoplasia IAGP N RGD:5509061 20190822 MGI PMID:31232685 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20190822 MGI PMID:31232685 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190822 MGI PMID:31232685 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0012174 flat head IAGP N RGD:5509061 20190815 MGI PMID:21515572 733102 Pgap2 post-GPI attachment to proteins 2 gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:31232685 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20190215 MGI PMID:30489685 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20130004 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:20130004 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20133599 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:20130004 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:20133599 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0002064 seizures IAGP N RGD:5509061 20190215 MGI PMID:30489685 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:20130004 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20133599 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20133599 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:20133599 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:20133599 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0003234 enhanced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20130004 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20130004 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20133599 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20133599 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:20130004 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20190215 MGI PMID:30489685 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0011002 enhanced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20130004 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20130004 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20659958 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0014372 decreased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:20133599 733104 Lgi1 leucine-rich repeat LGI family, member 1 gene MP:0014375 increased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:20130004 733106 Ctcf CCCTC-binding factor gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20240801 MGI PMID:38951485 733106 Ctcf CCCTC-binding factor gene MP:0001177 atelectasis IAGP N RGD:5509061 20240801 MGI PMID:38951485 733106 Ctcf CCCTC-binding factor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:22532833 733106 Ctcf CCCTC-binding factor gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18923423 733106 Ctcf CCCTC-binding factor gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18923423 733106 Ctcf CCCTC-binding factor gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20240801 MGI PMID:38951485 733106 Ctcf CCCTC-binding factor gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20240801 MGI PMID:38951485 733106 Ctcf CCCTC-binding factor gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20150212 MGI PMID:22532833 733106 Ctcf CCCTC-binding factor gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18923423 733106 Ctcf CCCTC-binding factor gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:18923423 733106 Ctcf CCCTC-binding factor gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18923423 733106 Ctcf CCCTC-binding factor gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20240801 MGI PMID:38951485 733106 Ctcf CCCTC-binding factor gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18923423 733106 Ctcf CCCTC-binding factor gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18923423 733106 Ctcf CCCTC-binding factor gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18923423 733106 Ctcf CCCTC-binding factor gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18923423 733106 Ctcf CCCTC-binding factor gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18923423 733106 Ctcf CCCTC-binding factor gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20240801 MGI PMID:38951485 733106 Ctcf CCCTC-binding factor gene MP:0008527 embryonic lethality at implantation IAGP N RGD:5509061 20141003 MGI PMID:22532833 733106 Ctcf CCCTC-binding factor gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20240801 MGI PMID:38951485 733106 Ctcf CCCTC-binding factor gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20240801 MGI PMID:38951485 733106 Ctcf CCCTC-binding factor gene MP:0010656 thick myocardium IAGP N RGD:5509061 20240801 MGI PMID:38951485 733106 Ctcf CCCTC-binding factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18923423 733106 Ctcf CCCTC-binding factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20240801 MGI PMID:38951485 733106 Ctcf CCCTC-binding factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18923423 733106 Ctcf CCCTC-binding factor gene MP:0012102 absent trophectoderm IAGP N RGD:5509061 20150212 MGI PMID:22532833 733106 Ctcf CCCTC-binding factor gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20240801 MGI PMID:38951485 733106 Ctcf CCCTC-binding factor gene MP:0013138 thin body IAGP N RGD:5509061 20240801 MGI PMID:38951485 733106 Ctcf CCCTC-binding factor gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:22532833 733106 Ctcf CCCTC-binding factor gene MP:0014519 myocardial ventricular hypertrabeculation IAGP N RGD:5509061 20240822 MGI PMID:38951485 733107 Gorasp1 golgi reassembly stacking protein 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210128 MGI 733107 Gorasp1 golgi reassembly stacking protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 733107 Gorasp1 golgi reassembly stacking protein 1 gene MP:0013243 abnormal carbohydrate metabolism IAGP N RGD:5509061 20160721 MGI PMID:24795147 733107 Gorasp1 golgi reassembly stacking protein 1 gene MP:0030954 abnormal Golgi cis cisterna morphology IAGP N RGD:5509061 20190725 MGI PMID:24795147 733109 Pcyox1 prenylcysteine oxidase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12151402 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:15365178 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15582159 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:15365178 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:15582159 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15365178 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15365178 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15582159 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15582159 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20150430 MGI PMID:25274777 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20150430 MGI PMID:25274777 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15582159 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15365173 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15365178 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15582159 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15582159 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20150430 MGI PMID:25274777 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20150430 MGI PMID:25274777 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:15582159 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:15582159 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20150430 MGI PMID:25274777 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20171207 MGI PMID:28859131 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15582159 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15582159 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20150430 MGI PMID:25274777 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20171207 MGI PMID:28859131 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0010749 absent visual evoked potential IAGP N RGD:5509061 20171207 MGI PMID:28859131 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20171207 MGI PMID:28859131 733112 Aipl1 aryl hydrocarbon receptor-interacting protein-like 1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:15365173 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:21816756 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:21816756 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:19729436 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:21816756 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:19233126 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19233126 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:19233126 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:19233126 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0002902 decreased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:19729436 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0002902 decreased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:21816756 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:19729436 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:19233126 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:19729436 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:19233126 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:19233126 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:21816756 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:21816756 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:21816756 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19729436 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:19233126 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:21816756 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0010923 calcified pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:19729436 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21816756 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19233126 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19233126 733114 Slc34a2 solute carrier family 34 (sodium phosphate), member 2 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:21816756 733117 Igfbp6 insulin-like growth factor binding protein 6 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 733118 Cxcl2 C-X-C motif chemokine ligand 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20170105 MGI 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15591342 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20190502 MGI 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:15282315 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:15591342 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15282315 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15282315 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15591342 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15282315 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:15282315 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0009709 hydrometra IEA N RGD:5509061 20190502 MGI 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15282315 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15591342 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 733120 Parg poly (ADP-ribose) glycohydrolase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 733124 Zfp597 zinc finger protein 597 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20190912 MGI PMID:19968752 733124 Zfp597 zinc finger protein 597 gene MP:0001393 ataxia IAGP N RGD:5509061 20190912 MGI PMID:19968752 733124 Zfp597 zinc finger protein 597 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20190912 MGI PMID:19968752 733124 Zfp597 zinc finger protein 597 gene MP:0002064 seizures IAGP N RGD:5509061 20190912 MGI PMID:19968752 733124 Zfp597 zinc finger protein 597 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20190912 MGI PMID:19968752 733124 Zfp597 zinc finger protein 597 gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20190912 MGI PMID:19968752 733124 Zfp597 zinc finger protein 597 gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20190912 MGI PMID:19968752 733124 Zfp597 zinc finger protein 597 gene MP:0004222 iris synechia IEA N RGD:5509061 20190502 MGI 733124 Zfp597 zinc finger protein 597 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20190912 MGI PMID:19968752 733124 Zfp597 zinc finger protein 597 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:19968752 733124 Zfp597 zinc finger protein 597 gene MP:0020749 abnormal cingulate cortex morphology IAGP N RGD:5509061 20190912 MGI PMID:19968752 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:2499515 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:3128974 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:3473481 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12420131 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:2499515 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:3128974 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:3473481 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12420131 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:3473481 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:3473481 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:10626891 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:10626891 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:10626891 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:12555678 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:14662903 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10626891 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12555678 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17641228 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:2499515 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:3473481 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12420131 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:2499515 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:3473481 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10626891 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:12555678 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10626891 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:10626891 733125 Tnfsf4 tumor necrosis factor (ligand) superfamily, member 4 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:10626891 733126 Impg1 interphotoreceptor matrix proteoglycan 1 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20210506 MGI PMID:32265257 733126 Impg1 interphotoreceptor matrix proteoglycan 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20210506 MGI PMID:32265257 733127 Tomm20 translocase of outer mitochondrial membrane 20 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 733127 Tomm20 translocase of outer mitochondrial membrane 20 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 733127 Tomm20 translocase of outer mitochondrial membrane 20 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20241024 MGI PMID:32376682 733127 Tomm20 translocase of outer mitochondrial membrane 20 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20241024 MGI PMID:32376682 733127 Tomm20 translocase of outer mitochondrial membrane 20 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733127 Tomm20 translocase of outer mitochondrial membrane 20 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 733127 Tomm20 translocase of outer mitochondrial membrane 20 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240919 MGI 733129 Vim vimentin gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:9294120 733129 Vim vimentin gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10712381 733129 Vim vimentin gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9625752 733129 Vim vimentin gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22031903 733129 Vim vimentin gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:22031903 733129 Vim vimentin gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:15662841 733129 Vim vimentin gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:9888296 733129 Vim vimentin gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:9888296 733129 Vim vimentin gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9888296 733129 Vim vimentin gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9888296 733129 Vim vimentin gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:9888296 733129 Vim vimentin gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12177195 733129 Vim vimentin gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:10225952 733129 Vim vimentin gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:9888296 733129 Vim vimentin gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:9888296 733129 Vim vimentin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:9888296 733129 Vim vimentin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9888296 733129 Vim vimentin gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:9888296 733129 Vim vimentin gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:9294120 733129 Vim vimentin gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16429129 733129 Vim vimentin gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:22031903 733129 Vim vimentin gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17525210 733129 Vim vimentin gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10225952 733129 Vim vimentin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22031903 733129 Vim vimentin gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:22031903 733129 Vim vimentin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25179606 733129 Vim vimentin gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:22031903 733129 Vim vimentin gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11701765 733129 Vim vimentin gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12177195 733129 Vim vimentin gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:17525210 733129 Vim vimentin gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22031903 733129 Vim vimentin gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:9888296 733129 Vim vimentin gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:9625752 733129 Vim vimentin gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:16429129 733129 Vim vimentin gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17525210 733129 Vim vimentin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:10225952 733129 Vim vimentin gene MP:0003627 abnormal leukocyte tethering or rolling IAGP N RGD:5509061 20141003 MGI PMID:16429129 733129 Vim vimentin gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:16429129 733129 Vim vimentin gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:22031903 733129 Vim vimentin gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9294120 733129 Vim vimentin gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:9294120 733129 Vim vimentin gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:10225952 733129 Vim vimentin gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9625752 733129 Vim vimentin gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22031903 733129 Vim vimentin gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:9888296 733129 Vim vimentin gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:22031903 733129 Vim vimentin gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11701765 733129 Vim vimentin gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9294120 733129 Vim vimentin gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:16429129 733129 Vim vimentin gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15662841 733129 Vim vimentin gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:20963821 733129 Vim vimentin gene MP:0012506 brain atrophy IAGP N RGD:5509061 20141003 MGI PMID:22031903 733132 Plaur plasminogen activator, urokinase receptor gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:12533622 733132 Plaur plasminogen activator, urokinase receptor gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11343646 733132 Plaur plasminogen activator, urokinase receptor gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12533622 733132 Plaur plasminogen activator, urokinase receptor gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:12533622 733132 Plaur plasminogen activator, urokinase receptor gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:20466854 733132 Plaur plasminogen activator, urokinase receptor gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:16554301 733132 Plaur plasminogen activator, urokinase receptor gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:20466854 733132 Plaur plasminogen activator, urokinase receptor gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11907112 733132 Plaur plasminogen activator, urokinase receptor gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:7622505 733132 Plaur plasminogen activator, urokinase receptor gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:8609247 733132 Plaur plasminogen activator, urokinase receptor gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:11907112 733132 Plaur plasminogen activator, urokinase receptor gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:15240745 733132 Plaur plasminogen activator, urokinase receptor gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:15240745 733132 Plaur plasminogen activator, urokinase receptor gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:20466854 733132 Plaur plasminogen activator, urokinase receptor gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:12533622 733132 Plaur plasminogen activator, urokinase receptor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16554301 733132 Plaur plasminogen activator, urokinase receptor gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:12533622 733132 Plaur plasminogen activator, urokinase receptor gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20141003 MGI PMID:12533622 733132 Plaur plasminogen activator, urokinase receptor gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20466854 733132 Plaur plasminogen activator, urokinase receptor gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11343646 733132 Plaur plasminogen activator, urokinase receptor gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11557572 733132 Plaur plasminogen activator, urokinase receptor gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:11343646 733132 Plaur plasminogen activator, urokinase receptor gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:11907112 733132 Plaur plasminogen activator, urokinase receptor gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 733132 Plaur plasminogen activator, urokinase receptor gene MP:0013498 trachea inflammation IAGP N RGD:5509061 20150212 MGI PMID:20466854 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15361866 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:15361866 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15361866 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0002223 lymphoid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15361866 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0002343 abnormal lymph node cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15361866 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:15361866 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:15361866 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15361866 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:15361866 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:21194982 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:15361866 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:15361866 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:15361866 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20810663 733134 Rassf5 Ras association (RalGDS/AF-6) domain family member 5 gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:20810663 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10742108 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:12032352 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:20610744 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:11756502 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10742108 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10742109 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:10742107 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:11337086 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:10742107 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12032352 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0001619 abnormal vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:10742109 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12746321 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:12832554 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12746321 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12746321 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12746321 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10742107 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12746321 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:10742107 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:10742108 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:11756502 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:10742107 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12746321 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:10742108 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:12746321 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12032352 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:12746321 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12746321 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0009136 decreased brown fat cell size IAGP N RGD:5509061 20141003 MGI PMID:12746321 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12746321 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0013366 adrenal gland atrophy IAGP N RGD:5509061 20230907 MGI PMID:11756502 733139 Crhr2 corticotropin releasing hormone receptor 2 gene MP:0014287 decreased adrenal gland zona fasciculata size IAGP N RGD:5509061 20230907 MGI PMID:11756502 733141 Rgcc regulator of cell cycle gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 733141 Rgcc regulator of cell cycle gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 733141 Rgcc regulator of cell cycle gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160204 MGI PMID:23695833 733141 Rgcc regulator of cell cycle gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210128 MGI 733141 Rgcc regulator of cell cycle gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 733141 Rgcc regulator of cell cycle gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20160204 MGI PMID:23695833 733141 Rgcc regulator of cell cycle gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20151126 MGI PMID:23695833 733141 Rgcc regulator of cell cycle gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20160204 MGI PMID:23695833 733141 Rgcc regulator of cell cycle gene MP:0004259 small placenta IAGP N RGD:5509061 20160204 MGI PMID:23695833 733141 Rgcc regulator of cell cycle gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20160204 MGI PMID:23695833 733141 Rgcc regulator of cell cycle gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 733141 Rgcc regulator of cell cycle gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20191107 MGI PMID:25770350 733141 Rgcc regulator of cell cycle gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20191107 MGI PMID:25770350 733141 Rgcc regulator of cell cycle gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20151126 MGI PMID:23695833 733141 Rgcc regulator of cell cycle gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20160204 MGI PMID:23695833 733141 Rgcc regulator of cell cycle gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20151126 MGI PMID:23695833 733141 Rgcc regulator of cell cycle gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20151126 MGI PMID:23695833 733141 Rgcc regulator of cell cycle gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20191107 MGI PMID:25770350 733141 Rgcc regulator of cell cycle gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20151126 MGI PMID:23695833 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17786210 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21056571 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21056571 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:21056571 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:21056571 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:21056571 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:17786210 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21056571 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17786210 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17786210 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:16354689 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:21056571 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0004043 abnormal pH regulation IAGP N RGD:5509061 20141003 MGI PMID:16354689 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:21056571 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21056571 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21056571 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21056571 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:21056571 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17786210 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:21056571 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17786210 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:21056571 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:21056571 733143 Slc4a3 solute carrier family 4 (anion exchanger), member 3 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:17786210 733144 Il9r interleukin 9 receptor gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 733144 Il9r interleukin 9 receptor gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 733144 Il9r interleukin 9 receptor gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 733144 Il9r interleukin 9 receptor gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 733144 Il9r interleukin 9 receptor gene MP:0001304 cataract IEA N RGD:5509061 20210520 MGI 733144 Il9r interleukin 9 receptor gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 733144 Il9r interleukin 9 receptor gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 733144 Il9r interleukin 9 receptor gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 733144 Il9r interleukin 9 receptor gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 733144 Il9r interleukin 9 receptor gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 733144 Il9r interleukin 9 receptor gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 733144 Il9r interleukin 9 receptor gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:19433802 733144 Il9r interleukin 9 receptor gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 733144 Il9r interleukin 9 receptor gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19433802 733144 Il9r interleukin 9 receptor gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:19433802 733144 Il9r interleukin 9 receptor gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 733145 Mcfd2 multiple coagulation factor deficiency 2 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20180906 MGI PMID:29735583 733145 Mcfd2 multiple coagulation factor deficiency 2 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20180906 MGI PMID:29735583 733145 Mcfd2 multiple coagulation factor deficiency 2 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20180906 MGI PMID:29735583 733145 Mcfd2 multiple coagulation factor deficiency 2 gene MP:0012328 decreased circulating factor VIII level IAGP N RGD:5509061 20180906 MGI PMID:29735583 733147 Tjp2 tight junction protein 2 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18172007 733147 Tjp2 tight junction protein 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0000601 small liver IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:18172007 733147 Tjp2 tight junction protein 2 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:18172007 733147 Tjp2 tight junction protein 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18172007 733147 Tjp2 tight junction protein 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18172007 733147 Tjp2 tight junction protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0003950 abnormal plasma membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:18172007 733147 Tjp2 tight junction protein 2 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:18172007 733147 Tjp2 tight junction protein 2 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0008991 abnormal bile canaliculus morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0009501 abnormal hepatic duct morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18172007 733147 Tjp2 tight junction protein 2 gene MP:0012246 abnormal hepatic cord morphology IAGP N RGD:5509061 20210722 MGI PMID:33184034 733147 Tjp2 tight junction protein 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:18172007 733148 C5ar1 complement component 5a receptor 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:8781237 733148 C5ar1 complement component 5a receptor 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8779720 733148 C5ar1 complement component 5a receptor 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:22430734 733148 C5ar1 complement component 5a receptor 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20200109 MGI PMID:23074214 733148 C5ar1 complement component 5a receptor 1 gene MP:0003981 decreased circulating phospholipid level IAGP N RGD:5509061 20200109 MGI PMID:23074214 733148 C5ar1 complement component 5a receptor 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:20709903 733148 C5ar1 complement component 5a receptor 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20200109 MGI PMID:23074214 733148 C5ar1 complement component 5a receptor 1 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20200109 MGI PMID:23074214 733148 C5ar1 complement component 5a receptor 1 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20200109 MGI PMID:23074214 733148 C5ar1 complement component 5a receptor 1 gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:18455242 733148 C5ar1 complement component 5a receptor 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200109 MGI PMID:23074214 733148 C5ar1 complement component 5a receptor 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200109 MGI PMID:23074214 733148 C5ar1 complement component 5a receptor 1 gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20200109 MGI PMID:23074214 733148 C5ar1 complement component 5a receptor 1 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20709903 733148 C5ar1 complement component 5a receptor 1 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:8779720 733148 C5ar1 complement component 5a receptor 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:8779720 733148 C5ar1 complement component 5a receptor 1 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200109 MGI PMID:23074214 733148 C5ar1 complement component 5a receptor 1 gene MP:0012040 abnormal c-wave shape IAGP N RGD:5509061 20200109 MGI PMID:23074214 733148 C5ar1 complement component 5a receptor 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200109 MGI PMID:23074214 733148 C5ar1 complement component 5a receptor 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200109 MGI PMID:23074214 733148 C5ar1 complement component 5a receptor 1 gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20200109 MGI PMID:23074214 733148 C5ar1 complement component 5a receptor 1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20200109 MGI PMID:23074214 733148 C5ar1 complement component 5a receptor 1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:23074214 733151 Trpc4 transient receptor potential cation channel, subfamily C, member 4 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20150226 MGI PMID:24599464 733151 Trpc4 transient receptor potential cation channel, subfamily C, member 4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 733151 Trpc4 transient receptor potential cation channel, subfamily C, member 4 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:23188715 733151 Trpc4 transient receptor potential cation channel, subfamily C, member 4 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20150226 MGI PMID:24599464 733151 Trpc4 transient receptor potential cation channel, subfamily C, member 4 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:11175743 733151 Trpc4 transient receptor potential cation channel, subfamily C, member 4 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20150226 MGI PMID:24599464 733153 Llgl1 LLGL1 scribble cell polarity complex component gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:15037549 733153 Llgl1 LLGL1 scribble cell polarity complex component gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:15037549 733153 Llgl1 LLGL1 scribble cell polarity complex component gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15037549 733153 Llgl1 LLGL1 scribble cell polarity complex component gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:15037549 733153 Llgl1 LLGL1 scribble cell polarity complex component gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:15037549 733153 Llgl1 LLGL1 scribble cell polarity complex component gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15037549 733153 Llgl1 LLGL1 scribble cell polarity complex component gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:15037549 733153 Llgl1 LLGL1 scribble cell polarity complex component gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15037549 733153 Llgl1 LLGL1 scribble cell polarity complex component gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:15037549 733153 Llgl1 LLGL1 scribble cell polarity complex component gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15037549 733153 Llgl1 LLGL1 scribble cell polarity complex component gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:15037549 733153 Llgl1 LLGL1 scribble cell polarity complex component gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:15037549 733153 Llgl1 LLGL1 scribble cell polarity complex component gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15037549 733153 Llgl1 LLGL1 scribble cell polarity complex component gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15037549 733153 Llgl1 LLGL1 scribble cell polarity complex component gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:15037549 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:17967447 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:18343643 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22223248 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:7493021 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20220714 MGI PMID:25358290 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:11960699 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11960699 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:11960699 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20231207 MGI 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20231207 MGI 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:10600892 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:12838410 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:7493021 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:17967447 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:22223248 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:7493021 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:18343643 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:18343643 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18343643 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22223248 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:7493021 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22223248 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20141003 MGI PMID:17967447 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0002726 abnormal pulmonary vein morphology IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:12838410 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17159989 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10600892 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12838410 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:17159989 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12838410 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10600892 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0004391 abnormal respiratory conducting tube morphology IAGP N RGD:5509061 20141003 MGI PMID:7493021 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18343643 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0005299 abnormal eye posterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:12838410 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:12838410 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12838410 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12838410 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:11960699 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:11984523 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:7493021 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20221013 MGI PMID:22223248 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20220714 MGI PMID:25358290 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0009874 abnormal interdigital cell death IAGP N RGD:5509061 20141003 MGI PMID:11960699 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:17967447 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0009889 persistence of medial edge epithelium during palatal shelf fusion IAGP N RGD:5509061 20141003 MGI PMID:7493021 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0009889 persistence of medial edge epithelium during palatal shelf fusion IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0009889 persistence of medial edge epithelium during palatal shelf fusion IAGP N RGD:5509061 20220714 MGI PMID:25358290 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221201 MGI PMID:18343643 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0010811 decreased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:10600892 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0010811 decreased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:10600892 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17967447 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18343643 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18343643 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22223248 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7493021 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160811 MGI 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18343643 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18343643 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:10600892 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:7493022 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:18343643 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0013531 abnormal periderm development IAGP N RGD:5509061 20220714 MGI PMID:25358290 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0014234 decreased enterocyte apoptosis IAGP N RGD:5509061 20230323 MGI PMID:11984523 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:22223248 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:7493021 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0021214 anterior cleft palate IAGP N RGD:5509061 20221201 MGI PMID:7493021 733158 Tgfb3 transforming growth factor, beta 3 gene MP:0030006 decreased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:12838410 733161 Nsf N-ethylmaleimide sensitive fusion protein gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 733161 Nsf N-ethylmaleimide sensitive fusion protein gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230601 MGI 733161 Nsf N-ethylmaleimide sensitive fusion protein gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20231012 MGI PMID:34745222 733161 Nsf N-ethylmaleimide sensitive fusion protein gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20231012 MGI PMID:34745222 733161 Nsf N-ethylmaleimide sensitive fusion protein gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20231012 MGI PMID:34745222 733161 Nsf N-ethylmaleimide sensitive fusion protein gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20201022 MGI 733161 Nsf N-ethylmaleimide sensitive fusion protein gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20211021 MGI 733161 Nsf N-ethylmaleimide sensitive fusion protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20231012 MGI PMID:34745222 733161 Nsf N-ethylmaleimide sensitive fusion protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733161 Nsf N-ethylmaleimide sensitive fusion protein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 733161 Nsf N-ethylmaleimide sensitive fusion protein gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 733161 Nsf N-ethylmaleimide sensitive fusion protein gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20231012 MGI PMID:34745222 733161 Nsf N-ethylmaleimide sensitive fusion protein gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20231012 MGI PMID:34745222 733161 Nsf N-ethylmaleimide sensitive fusion protein gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220811 MGI 733161 Nsf N-ethylmaleimide sensitive fusion protein gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20231012 MGI PMID:34745222 733162 Ebp EBP cholestenol delta-isomerase gene MP:0000414 alopecia IEA N RGD:5509061 20111116 MGI 733162 Ebp EBP cholestenol delta-isomerase gene MP:0001195 flaky skin IEA N RGD:5509061 20111116 MGI 733162 Ebp EBP cholestenol delta-isomerase gene MP:0001212 skin lesions IEA N RGD:5509061 20111116 MGI 733162 Ebp EBP cholestenol delta-isomerase gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:9250864 733162 Ebp EBP cholestenol delta-isomerase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9250864 733162 Ebp EBP cholestenol delta-isomerase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9250864 733162 Ebp EBP cholestenol delta-isomerase gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10987663 733162 Ebp EBP cholestenol delta-isomerase gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:10987663 733162 Ebp EBP cholestenol delta-isomerase gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10987663 733162 Ebp EBP cholestenol delta-isomerase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:9250864 733162 Ebp EBP cholestenol delta-isomerase gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 733162 Ebp EBP cholestenol delta-isomerase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9250864 733162 Ebp EBP cholestenol delta-isomerase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9250864 733162 Ebp EBP cholestenol delta-isomerase gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 733166 Riox2 ribosomal oxygenase 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23748603 733166 Riox2 ribosomal oxygenase 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23748603 733166 Riox2 ribosomal oxygenase 2 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:23748603 733166 Riox2 ribosomal oxygenase 2 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:23748603 733166 Riox2 ribosomal oxygenase 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:23748603 733166 Riox2 ribosomal oxygenase 2 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23748603 733166 Riox2 ribosomal oxygenase 2 gene MP:0008551 abnormal circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:23748603 733166 Riox2 ribosomal oxygenase 2 gene MP:0008601 abnormal circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:23748603 733166 Riox2 ribosomal oxygenase 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23748603 733167 Pom121 nuclear pore membrane protein 121 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200402 MGI 733167 Pom121 nuclear pore membrane protein 121 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733167 Pom121 nuclear pore membrane protein 121 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 733167 Pom121 nuclear pore membrane protein 121 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220811 MGI 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0000601 small liver IEA N RGD:5509061 20220811 MGI 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220811 MGI 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220811 MGI 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0000774 decreased brain size IEA N RGD:5509061 20220811 MGI 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220811 MGI 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20220811 MGI 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20220811 MGI 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0011939 increased food intake IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0013243 abnormal carbohydrate metabolism IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20160728 MGI PMID:26049045 733169 Fmo5 flavin containing monooxygenase 5 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20160728 MGI PMID:26049045 733171 Acsl3 acyl-CoA synthetase long-chain family member 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20141003 MGI 733171 Acsl3 acyl-CoA synthetase long-chain family member 3 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 733171 Acsl3 acyl-CoA synthetase long-chain family member 3 gene MP:0001732 postnatal growth retardation IEA N RGD:5509061 20141003 MGI 733171 Acsl3 acyl-CoA synthetase long-chain family member 3 gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20141003 MGI 733171 Acsl3 acyl-CoA synthetase long-chain family member 3 gene MP:0002089 abnormal postnatal growth/weight/body size IEA N RGD:5509061 20141003 MGI 733171 Acsl3 acyl-CoA synthetase long-chain family member 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20141003 MGI 733171 Acsl3 acyl-CoA synthetase long-chain family member 3 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20141003 MGI 733171 Acsl3 acyl-CoA synthetase long-chain family member 3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20141003 MGI 733172 Ctrl chymotrypsin-like gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20200924 MGI PMID:32678161 733173 Rab10 RAB10, member RAS oncogene family gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20180927 MGI PMID:25860786 733173 Rab10 RAB10, member RAS oncogene family gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 733173 Rab10 RAB10, member RAS oncogene family gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20180927 MGI PMID:25860786 733173 Rab10 RAB10, member RAS oncogene family gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20180927 MGI PMID:25860786 733173 Rab10 RAB10, member RAS oncogene family gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180927 MGI PMID:25860786 733173 Rab10 RAB10, member RAS oncogene family gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20180927 MGI PMID:25860786 733173 Rab10 RAB10, member RAS oncogene family gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20190919 MGI PMID:27207531 733173 Rab10 RAB10, member RAS oncogene family gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20180927 MGI PMID:25860786 733173 Rab10 RAB10, member RAS oncogene family gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 733173 Rab10 RAB10, member RAS oncogene family gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20180927 MGI PMID:25860786 733173 Rab10 RAB10, member RAS oncogene family gene MP:0004222 iris synechia IEA N RGD:5509061 20190502 MGI 733173 Rab10 RAB10, member RAS oncogene family gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 733173 Rab10 RAB10, member RAS oncogene family gene MP:0005331 insulin resistance IAGP N RGD:5509061 20190919 MGI PMID:27207531 733173 Rab10 RAB10, member RAS oncogene family gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 733173 Rab10 RAB10, member RAS oncogene family gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20180927 MGI PMID:25860786 733173 Rab10 RAB10, member RAS oncogene family gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20180927 MGI PMID:25860786 733173 Rab10 RAB10, member RAS oncogene family gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733173 Rab10 RAB10, member RAS oncogene family gene MP:0011207 absent ectoplacental cavity IAGP N RGD:5509061 20180927 MGI PMID:25860786 733173 Rab10 RAB10, member RAS oncogene family gene MP:0011209 absent extraembryonic coelom IAGP N RGD:5509061 20180927 MGI PMID:25860786 733173 Rab10 RAB10, member RAS oncogene family gene MP:0012142 absent amniotic cavity IAGP N RGD:5509061 20180927 MGI PMID:25860786 733173 Rab10 RAB10, member RAS oncogene family gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 733173 Rab10 RAB10, member RAS oncogene family gene MP:0020102 increased hepatic glucose production IAGP N RGD:5509061 20190919 MGI PMID:27207531 733173 Rab10 RAB10, member RAS oncogene family gene MP:0020851 abnormal vacuole morphology IAGP N RGD:5509061 20230615 MGI PMID:25860786 733173 Rab10 RAB10, member RAS oncogene family gene MP:0030017 decreased adipocyte glucose uptake IAGP N RGD:5509061 20190919 MGI PMID:27207531 733174 Plau plasminogen activator, urokinase gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 733174 Plau plasminogen activator, urokinase gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20231207 MGI 733174 Plau plasminogen activator, urokinase gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20141003 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:11760891 733174 Plau plasminogen activator, urokinase gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:11760891 733174 Plau plasminogen activator, urokinase gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:11760891 733174 Plau plasminogen activator, urokinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:11059781 733174 Plau plasminogen activator, urokinase gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220811 MGI 733174 Plau plasminogen activator, urokinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:20466854 733174 Plau plasminogen activator, urokinase gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:20466854 733174 Plau plasminogen activator, urokinase gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11238111 733174 Plau plasminogen activator, urokinase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11025665 733174 Plau plasminogen activator, urokinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20466854 733174 Plau plasminogen activator, urokinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:20466854 733174 Plau plasminogen activator, urokinase gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:11777975 733174 Plau plasminogen activator, urokinase gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:14688127 733174 Plau plasminogen activator, urokinase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:11907112 733174 Plau plasminogen activator, urokinase gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:15240745 733174 Plau plasminogen activator, urokinase gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:15240745 733174 Plau plasminogen activator, urokinase gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:20466854 733174 Plau plasminogen activator, urokinase gene MP:0002964 aortic elastic tissue lesions IAGP N RGD:5509061 20141003 MGI PMID:9398846 733174 Plau plasminogen activator, urokinase gene MP:0003315 abnormal perineum morphology IAGP N RGD:5509061 20141003 MGI PMID:11760891 733174 Plau plasminogen activator, urokinase gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20466854 733174 Plau plasminogen activator, urokinase gene MP:0003423 reduced thrombolysis IAGP N RGD:5509061 20141003 MGI PMID:10961882 733174 Plau plasminogen activator, urokinase gene MP:0003423 reduced thrombolysis IAGP N RGD:5509061 20141003 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0003426 pulmonary interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10880388 733174 Plau plasminogen activator, urokinase gene MP:0003434 decreased susceptibility to induced choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:12657615 733174 Plau plasminogen activator, urokinase gene MP:0003435 herniated seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:11760891 733174 Plau plasminogen activator, urokinase gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:11891190 733174 Plau plasminogen activator, urokinase gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:11059781 733174 Plau plasminogen activator, urokinase gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:11059781 733174 Plau plasminogen activator, urokinase gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10880388 733174 Plau plasminogen activator, urokinase gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:11238111 733174 Plau plasminogen activator, urokinase gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20240704 MGI PMID:15631996 733174 Plau plasminogen activator, urokinase gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10880388 733174 Plau plasminogen activator, urokinase gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:14688127 733174 Plau plasminogen activator, urokinase gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0005074 impaired granulocyte bactericidal activity IAGP N RGD:5509061 20141003 MGI PMID:15240745 733174 Plau plasminogen activator, urokinase gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11891190 733174 Plau plasminogen activator, urokinase gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:20466854 733174 Plau plasminogen activator, urokinase gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:20466854 733174 Plau plasminogen activator, urokinase gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9398846 733174 Plau plasminogen activator, urokinase gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:8621764 733174 Plau plasminogen activator, urokinase gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:15615772 733174 Plau plasminogen activator, urokinase gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15631996 733174 Plau plasminogen activator, urokinase gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:11891190 733174 Plau plasminogen activator, urokinase gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:9576763 733174 Plau plasminogen activator, urokinase gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20466854 733174 Plau plasminogen activator, urokinase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20466854 733174 Plau plasminogen activator, urokinase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 733174 Plau plasminogen activator, urokinase gene MP:0010211 abnormal acute phase protein level IAGP N RGD:5509061 20141003 MGI PMID:10880388 733174 Plau plasminogen activator, urokinase gene MP:0010211 abnormal acute phase protein level IAGP N RGD:5509061 20141003 MGI PMID:11238111 733174 Plau plasminogen activator, urokinase gene MP:0010211 abnormal acute phase protein level IAGP N RGD:5509061 20141003 MGI PMID:12657615 733174 Plau plasminogen activator, urokinase gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:20466854 733174 Plau plasminogen activator, urokinase gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:11238111 733174 Plau plasminogen activator, urokinase gene MP:0013498 trachea inflammation IAGP N RGD:5509061 20150212 MGI PMID:20466854 733174 Plau plasminogen activator, urokinase gene MP:0013499 trachea fibrosis IAGP N RGD:5509061 20150212 MGI PMID:20466854 733174 Plau plasminogen activator, urokinase gene MP:0030530 abnormal outer ear skin morphology IAGP N RGD:5509061 20180118 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0030531 abnormal facial skin morphology IAGP N RGD:5509061 20180118 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:8133887 733174 Plau plasminogen activator, urokinase gene MP:0031635 increased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15631996 733175 S100a9 S100 calcium binding protein A9 (calgranulin B) gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:12640137 733175 S100a9 S100 calcium binding protein A9 (calgranulin B) gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20141003 MGI PMID:12640137 733175 S100a9 S100 calcium binding protein A9 (calgranulin B) gene MP:0005398 decreased susceptibility to fungal infection IAGP N RGD:5509061 20200618 MGI PMID:24478092 733175 S100a9 S100 calcium binding protein A9 (calgranulin B) gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17767165 733175 S100a9 S100 calcium binding protein A9 (calgranulin B) gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17767165 733175 S100a9 S100 calcium binding protein A9 (calgranulin B) gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17767165 733175 S100a9 S100 calcium binding protein A9 (calgranulin B) gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:12529407 733175 S100a9 S100 calcium binding protein A9 (calgranulin B) gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23132931 733176 Prl7b1 prolactin family 7, subfamily b, member 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20221215 MGI 733176 Prl7b1 prolactin family 7, subfamily b, member 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20180208 MGI PMID:26985002 733176 Prl7b1 prolactin family 7, subfamily b, member 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20180208 MGI PMID:26985002 733176 Prl7b1 prolactin family 7, subfamily b, member 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20221215 MGI 733176 Prl7b1 prolactin family 7, subfamily b, member 1 gene MP:0009432 increased fetal weight IAGP N RGD:5509061 20180208 MGI PMID:26985002 733178 Idh3a isocitrate dehydrogenase 3 (NAD+) alpha gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20160929 MGI PMID:27534441 733178 Idh3a isocitrate dehydrogenase 3 (NAD+) alpha gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20240404 MGI PMID:30478029 733178 Idh3a isocitrate dehydrogenase 3 (NAD+) alpha gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:30478029 733178 Idh3a isocitrate dehydrogenase 3 (NAD+) alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 733178 Idh3a isocitrate dehydrogenase 3 (NAD+) alpha gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20240523 MGI 733178 Idh3a isocitrate dehydrogenase 3 (NAD+) alpha gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20240523 MGI 733178 Idh3a isocitrate dehydrogenase 3 (NAD+) alpha gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:27534441 733178 Idh3a isocitrate dehydrogenase 3 (NAD+) alpha gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:30478029 733181 Aldh3a1 aldehyde dehydrogenase family 3, subfamily A1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11784860 733183 Crx cone-rod homeobox gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 733183 Crx cone-rod homeobox gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 733183 Crx cone-rod homeobox gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 733183 Crx cone-rod homeobox gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 733183 Crx cone-rod homeobox gene MP:0000706 small thymus IEA N RGD:5509061 20210128 MGI 733183 Crx cone-rod homeobox gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 733183 Crx cone-rod homeobox gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:10581037 733183 Crx cone-rod homeobox gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:24382353 733183 Crx cone-rod homeobox gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20160623 MGI PMID:25757744 733183 Crx cone-rod homeobox gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20160128 MGI PMID:24516401 733183 Crx cone-rod homeobox gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210128 MGI 733183 Crx cone-rod homeobox gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 733183 Crx cone-rod homeobox gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:10581037 733183 Crx cone-rod homeobox gene MP:0001326 retina degeneration IEA N RGD:5509061 20240606 MGI 733183 Crx cone-rod homeobox gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 733183 Crx cone-rod homeobox gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:24382353 733183 Crx cone-rod homeobox gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210128 MGI 733183 Crx cone-rod homeobox gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 733183 Crx cone-rod homeobox gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:24382353 733183 Crx cone-rod homeobox gene MP:0002764 short tibia IEA N RGD:5509061 20220811 MGI 733183 Crx cone-rod homeobox gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:21052544 733183 Crx cone-rod homeobox gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20160128 MGI PMID:24516401 733183 Crx cone-rod homeobox gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10581037 733183 Crx cone-rod homeobox gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24382353 733183 Crx cone-rod homeobox gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:10581037 733183 Crx cone-rod homeobox gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15676071 733183 Crx cone-rod homeobox gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15676071 733183 Crx cone-rod homeobox gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20160128 MGI PMID:24516401 733183 Crx cone-rod homeobox gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15676071 733183 Crx cone-rod homeobox gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20160623 MGI PMID:25757744 733183 Crx cone-rod homeobox gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10581037 733183 Crx cone-rod homeobox gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:24382353 733183 Crx cone-rod homeobox gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20240425 MGI PMID:37963072 733183 Crx cone-rod homeobox gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10581037 733183 Crx cone-rod homeobox gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:24382353 733183 Crx cone-rod homeobox gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20240425 MGI PMID:37963072 733183 Crx cone-rod homeobox gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21052544 733183 Crx cone-rod homeobox gene MP:0005391 vision/eye phenotype IAGP N RGD:5509061 20240208 MGI PMID:37963072 733183 Crx cone-rod homeobox gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10581037 733183 Crx cone-rod homeobox gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14730587 733183 Crx cone-rod homeobox gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20240208 MGI PMID:37963072 733183 Crx cone-rod homeobox gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14730587 733183 Crx cone-rod homeobox gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20160623 MGI PMID:25757744 733183 Crx cone-rod homeobox gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14730587 733183 Crx cone-rod homeobox gene MP:0006075 abnormal retina cone bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14730587 733183 Crx cone-rod homeobox gene MP:0006148 binocular blindness IAGP N RGD:5509061 20240208 MGI PMID:37963072 733183 Crx cone-rod homeobox gene MP:0008044 increased NK cell number IEA N RGD:5509061 20230601 MGI 733183 Crx cone-rod homeobox gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20160128 MGI PMID:24516401 733183 Crx cone-rod homeobox gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21052544 733183 Crx cone-rod homeobox gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:10581037 733183 Crx cone-rod homeobox gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:14730587 733183 Crx cone-rod homeobox gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20240208 MGI PMID:37963072 733183 Crx cone-rod homeobox gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:21052544 733183 Crx cone-rod homeobox gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20160128 MGI PMID:24516401 733183 Crx cone-rod homeobox gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:21052544 733183 Crx cone-rod homeobox gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:24382353 733183 Crx cone-rod homeobox gene MP:0008583 absent photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:21052544 733183 Crx cone-rod homeobox gene MP:0008583 absent photoreceptor inner segment IAGP N RGD:5509061 20160623 MGI PMID:25757744 733183 Crx cone-rod homeobox gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:10581037 733183 Crx cone-rod homeobox gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:21052544 733183 Crx cone-rod homeobox gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:24382353 733183 Crx cone-rod homeobox gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20160128 MGI PMID:24516401 733183 Crx cone-rod homeobox gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20240208 MGI PMID:37963072 733183 Crx cone-rod homeobox gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:24382353 733183 Crx cone-rod homeobox gene MP:0010749 absent visual evoked potential IAGP N RGD:5509061 20240208 MGI PMID:37963072 733183 Crx cone-rod homeobox gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210128 MGI 733183 Crx cone-rod homeobox gene MP:0011997 abnormal retina outer nuclear layer thickness IAGP N RGD:5509061 20160128 MGI PMID:24516401 733183 Crx cone-rod homeobox gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20160128 MGI PMID:24516401 733183 Crx cone-rod homeobox gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20160128 MGI PMID:24516401 733183 Crx cone-rod homeobox gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20240425 MGI PMID:37963072 733183 Crx cone-rod homeobox gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20160128 MGI PMID:24516401 733183 Crx cone-rod homeobox gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20240425 MGI PMID:37963072 733183 Crx cone-rod homeobox gene MP:0012671 retina spots IAGP N RGD:5509061 20141003 MGI PMID:24382353 733183 Crx cone-rod homeobox gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 733183 Crx cone-rod homeobox gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:24516401 733183 Crx cone-rod homeobox gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:10581037 733183 Crx cone-rod homeobox gene MP:0020475 delayed circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:10581037 733184 Uncx UNC homeobox gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0000139 absent vertebral transverse processes IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0000140 absent vertebral pedicles IAGP N RGD:5509061 20141003 MGI PMID:10804168 733184 Uncx UNC homeobox gene MP:0000140 absent vertebral pedicles IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0000152 absent proximal rib IAGP N RGD:5509061 20141003 MGI PMID:10804168 733184 Uncx UNC homeobox gene MP:0000152 absent proximal rib IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:10804168 733184 Uncx UNC homeobox gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10804168 733184 Uncx UNC homeobox gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10804168 733184 Uncx UNC homeobox gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0000962 disorganized dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:10804168 733184 Uncx UNC homeobox gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:10804168 733184 Uncx UNC homeobox gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10804168 733184 Uncx UNC homeobox gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10804168 733184 Uncx UNC homeobox gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10804168 733184 Uncx UNC homeobox gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:10804168 733184 Uncx UNC homeobox gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0004612 fusion of vertebral bodies IAGP N RGD:5509061 20141003 MGI PMID:10804168 733184 Uncx UNC homeobox gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:10804168 733184 Uncx UNC homeobox gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:10804168 733184 Uncx UNC homeobox gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0008147 asymmetric costovertebral joints IAGP N RGD:5509061 20141003 MGI PMID:10804169 733184 Uncx UNC homeobox gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10804168 733184 Uncx UNC homeobox gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10804169 733185 Spag11a sperm associated antigen 11A gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20230601 MGI 733185 Spag11a sperm associated antigen 11A gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230601 MGI 733185 Spag11a sperm associated antigen 11A gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 733189 Taldo1 transaldolase 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:17003133 733189 Taldo1 transaldolase 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17003133 733189 Taldo1 transaldolase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17003133 733189 Taldo1 transaldolase 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17003133 733189 Taldo1 transaldolase 1 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:17003133 733189 Taldo1 transaldolase 1 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:17003133 733189 Taldo1 transaldolase 1 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:17003133 733189 Taldo1 transaldolase 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:17003133 733189 Taldo1 transaldolase 1 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:17003133 733191 Hspa4 heat shock protein 4 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:21487003 733191 Hspa4 heat shock protein 4 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21487003 733191 Hspa4 heat shock protein 4 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20679486 733191 Hspa4 heat shock protein 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21487003 733191 Hspa4 heat shock protein 4 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:20679486 733191 Hspa4 heat shock protein 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20679486 733191 Hspa4 heat shock protein 4 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21487003 733191 Hspa4 heat shock protein 4 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:20679486 733191 Hspa4 heat shock protein 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21487003 733191 Hspa4 heat shock protein 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21487003 733191 Hspa4 heat shock protein 4 gene MP:0003214 neurofibrillary tangles IAGP N RGD:5509061 20141003 MGI PMID:20679486 733191 Hspa4 heat shock protein 4 gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20141003 MGI PMID:20679486 733191 Hspa4 heat shock protein 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21487003 733191 Hspa4 heat shock protein 4 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21487003 733191 Hspa4 heat shock protein 4 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:21487003 733191 Hspa4 heat shock protein 4 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:21487003 733191 Hspa4 heat shock protein 4 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:20679486 733191 Hspa4 heat shock protein 4 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:21487003 733194 Rasgrp4 RAS guanyl releasing protein 4 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 733194 Rasgrp4 RAS guanyl releasing protein 4 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:22728827 733194 Rasgrp4 RAS guanyl releasing protein 4 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 733194 Rasgrp4 RAS guanyl releasing protein 4 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:22511759 733194 Rasgrp4 RAS guanyl releasing protein 4 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:22511759 733194 Rasgrp4 RAS guanyl releasing protein 4 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:22728827 733196 Mpp4 membrane protein, palmitoylated 4 (MAGUK p55 subfamily member 4) gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:17341488 733196 Mpp4 membrane protein, palmitoylated 4 (MAGUK p55 subfamily member 4) gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:16520334 733196 Mpp4 membrane protein, palmitoylated 4 (MAGUK p55 subfamily member 4) gene MP:0003950 abnormal plasma membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16520334 733196 Mpp4 membrane protein, palmitoylated 4 (MAGUK p55 subfamily member 4) gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17341488 733199 Top1 topoisomerase (DNA) I gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8943335 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0012557 decreased calcium uptake by cardiac muscle IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0014046 abnormal mitophagy IAGP N RGD:5509061 20161201 MGI PMID:25738458 733201 Cdk5rap1 CDK5 regulatory subunit associated protein 1 gene MP:0014394 increased skeletal muscle fiber mitochondrial DNA content IAGP N RGD:5509061 20240328 MGI PMID:25738458 733202 Ube2g1 ubiquitin-conjugating enzyme E2G 1 gene MP:0000601 small liver IEA N RGD:5509061 20170105 MGI 733202 Ube2g1 ubiquitin-conjugating enzyme E2G 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 733202 Ube2g1 ubiquitin-conjugating enzyme E2G 1 gene MP:0002764 short tibia IEA N RGD:5509061 20161201 MGI 733202 Ube2g1 ubiquitin-conjugating enzyme E2G 1 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20201231 MGI 733202 Ube2g1 ubiquitin-conjugating enzyme E2G 1 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20161201 MGI 733202 Ube2g1 ubiquitin-conjugating enzyme E2G 1 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20201231 MGI 733202 Ube2g1 ubiquitin-conjugating enzyme E2G 1 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20201231 MGI 733202 Ube2g1 ubiquitin-conjugating enzyme E2G 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 733203 Cux1 cut-like homeobox 1 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0000381 enlarged hair follicles IAGP N RGD:5509061 20141003 MGI PMID:11839809 733203 Cux1 cut-like homeobox 1 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:9698457 733203 Cux1 cut-like homeobox 1 gene MP:0000388 absent hair follicle inner root sheath IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:11839809 733203 Cux1 cut-like homeobox 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0000711 thymus cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:9698457 733203 Cux1 cut-like homeobox 1 gene MP:0001278 kinked vibrissae IAGP N RGD:5509061 20141003 MGI PMID:9698457 733203 Cux1 cut-like homeobox 1 gene MP:0001279 wavy vibrissae IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11839809 733203 Cux1 cut-like homeobox 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0001867 rhinitis IAGP N RGD:5509061 20141003 MGI PMID:11839809 733203 Cux1 cut-like homeobox 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15143175 733203 Cux1 cut-like homeobox 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11839809 733203 Cux1 cut-like homeobox 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11839809 733203 Cux1 cut-like homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15143175 733203 Cux1 cut-like homeobox 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0002271 abnormal pulmonary alveolar duct morphology IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0002324 abnormal alveolocapillary membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11839809 733203 Cux1 cut-like homeobox 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:11839809 733203 Cux1 cut-like homeobox 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:18829740 733203 Cux1 cut-like homeobox 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18829740 733203 Cux1 cut-like homeobox 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:18829740 733203 Cux1 cut-like homeobox 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:9698457 733203 Cux1 cut-like homeobox 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18829740 733203 Cux1 cut-like homeobox 1 gene MP:0006363 absent auchene hairs IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0006364 absent awl hair IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0006365 absent guard hair IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0006366 absent zigzag hairs IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0008779 abnormal maternal behavior IAGP N RGD:5509061 20141003 MGI PMID:9698457 733203 Cux1 cut-like homeobox 1 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:18033766 733203 Cux1 cut-like homeobox 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15143175 733203 Cux1 cut-like homeobox 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11544187 733203 Cux1 cut-like homeobox 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11739170 733203 Cux1 cut-like homeobox 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18033766 733203 Cux1 cut-like homeobox 1 gene MP:0012110 increased hair follicle number IAGP N RGD:5509061 20181129 MGI PMID:11739170 733204 Epha5 Eph receptor A5 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15014130 733204 Epha5 Eph receptor A5 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 733204 Epha5 Eph receptor A5 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0011408 renal tubule hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0011527 disorganized placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0011843 abnormal kidney collecting duct epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0012098 increased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:18048640 733207 Hsd17b2 hydroxysteroid (17-beta) dehydrogenase 2 gene MP:0020526 enlarged thalamus IAGP N RGD:5509061 20180208 MGI PMID:18048640 733208 Cnga4 cyclic nucleotide gated channel alpha 4 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11739959 733208 Cnga4 cyclic nucleotide gated channel alpha 4 gene MP:0009562 abnormal odor adaptation IAGP N RGD:5509061 20141003 MGI PMID:11739959 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11483953 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10611374 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10624962 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23894296 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10611374 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10624962 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11483953 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10611374 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10624962 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:10624962 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:10611374 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11483953 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10611374 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10624962 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23894296 733212 Sv2a synaptic vesicle glycoprotein 2a gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10624962 733214 Tpo thyroid peroxidase gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:24297261 733214 Tpo thyroid peroxidase gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:16762971 733214 Tpo thyroid peroxidase gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20200514 MGI 733214 Tpo thyroid peroxidase gene MP:0000550 abnormal forelimb morphology IEA N RGD:5509061 20200514 MGI 733214 Tpo thyroid peroxidase gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20200514 MGI 733214 Tpo thyroid peroxidase gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:24297261 733214 Tpo thyroid peroxidase gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:24297261 733214 Tpo thyroid peroxidase gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:16762971 733214 Tpo thyroid peroxidase gene MP:0000745 tremors IEA N RGD:5509061 20200514 MGI 733214 Tpo thyroid peroxidase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16762971 733214 Tpo thyroid peroxidase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16762971 733214 Tpo thyroid peroxidase gene MP:0001406 abnormal gait IEA N RGD:5509061 20200514 MGI 733214 Tpo thyroid peroxidase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 733214 Tpo thyroid peroxidase gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200514 MGI 733214 Tpo thyroid peroxidase gene MP:0001513 limb grasping IEA N RGD:5509061 20200514 MGI 733214 Tpo thyroid peroxidase gene MP:0001523 impaired righting response IEA N RGD:5509061 20200514 MGI 733214 Tpo thyroid peroxidase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16762971 733214 Tpo thyroid peroxidase gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:16762971 733214 Tpo thyroid peroxidase gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20200514 MGI 733214 Tpo thyroid peroxidase gene MP:0002750 exophthalmos IAGP N RGD:5509061 20170914 MGI PMID:16762971 733214 Tpo thyroid peroxidase gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16762971 733214 Tpo thyroid peroxidase gene MP:0002876 abnormal thyroid gland physiology IAGP N RGD:5509061 20141003 MGI PMID:24297261 733214 Tpo thyroid peroxidase gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:24297261 733214 Tpo thyroid peroxidase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 733214 Tpo thyroid peroxidase gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:24297261 733214 Tpo thyroid peroxidase gene MP:0003421 abnormal thyroid gland development IAGP N RGD:5509061 20141003 MGI PMID:24297261 733214 Tpo thyroid peroxidase gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:24297261 733214 Tpo thyroid peroxidase gene MP:0004664 delayed inner ear development IAGP N RGD:5509061 20141003 MGI PMID:24297261 733214 Tpo thyroid peroxidase gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16762971 733214 Tpo thyroid peroxidase gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:24297261 733214 Tpo thyroid peroxidase gene MP:0004697 abnormal thyroid follicular cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16762971 733214 Tpo thyroid peroxidase gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:16762971 733214 Tpo thyroid peroxidase gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20230601 MGI 733214 Tpo thyroid peroxidase gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20220811 MGI 733214 Tpo thyroid peroxidase gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 733214 Tpo thyroid peroxidase gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:16762971 733214 Tpo thyroid peroxidase gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230601 MGI 733214 Tpo thyroid peroxidase gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 733214 Tpo thyroid peroxidase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16762971 733214 Tpo thyroid peroxidase gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20230601 MGI 733214 Tpo thyroid peroxidase gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:24297261 733214 Tpo thyroid peroxidase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 733214 Tpo thyroid peroxidase gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:24297261 733214 Tpo thyroid peroxidase gene MP:0030049 prominent forehead IAGP N RGD:5509061 20170921 MGI PMID:16762971 733216 Phka1 phosphorylase kinase alpha 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 733216 Phka1 phosphorylase kinase alpha 1 gene MP:0000692 small spleen IEA N RGD:5509061 20220519 MGI 733216 Phka1 phosphorylase kinase alpha 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220519 MGI 733216 Phka1 phosphorylase kinase alpha 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 733216 Phka1 phosphorylase kinase alpha 1 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:5444100 733217 Cs citrate synthase gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20181227 MGI 733217 Cs citrate synthase gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:18280008 733217 Cs citrate synthase gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 733217 Cs citrate synthase gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:18280008 733217 Cs citrate synthase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 733217 Cs citrate synthase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 733217 Cs citrate synthase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733217 Cs citrate synthase gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18280008 733217 Cs citrate synthase gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20180329 MGI PMID:21803452 733221 Lmnb1 lamin B1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15232008 733221 Lmnb1 lamin B1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20160804 MGI 733221 Lmnb1 lamin B1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15232008 733221 Lmnb1 lamin B1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:22116031 733221 Lmnb1 lamin B1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15232008 733221 Lmnb1 lamin B1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:23650370 733221 Lmnb1 lamin B1 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:22116031 733221 Lmnb1 lamin B1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:23650370 733221 Lmnb1 lamin B1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22116031 733221 Lmnb1 lamin B1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23650370 733221 Lmnb1 lamin B1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:15232008 733221 Lmnb1 lamin B1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:23650370 733221 Lmnb1 lamin B1 gene MP:0001184 absent pulmonary alveoli IAGP N RGD:5509061 20141003 MGI PMID:15232008 733221 Lmnb1 lamin B1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 733221 Lmnb1 lamin B1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15232008 733221 Lmnb1 lamin B1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22116031 733221 Lmnb1 lamin B1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:15232008 733221 Lmnb1 lamin B1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:22116031 733221 Lmnb1 lamin B1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:22116031 733221 Lmnb1 lamin B1 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21659336 733221 Lmnb1 lamin B1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23650370 733221 Lmnb1 lamin B1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 733221 Lmnb1 lamin B1 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15232008 733221 Lmnb1 lamin B1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15232008 733221 Lmnb1 lamin B1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:23650370 733221 Lmnb1 lamin B1 gene MP:0003840 abnormal coronal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:15232008 733221 Lmnb1 lamin B1 gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:15232008 733221 Lmnb1 lamin B1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20210610 MGI PMID:15232008 733221 Lmnb1 lamin B1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:22116031 733221 Lmnb1 lamin B1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:22116031 733221 Lmnb1 lamin B1 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:22116031 733221 Lmnb1 lamin B1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15232008 733221 Lmnb1 lamin B1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 733221 Lmnb1 lamin B1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22116031 733221 Lmnb1 lamin B1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:22116031 733221 Lmnb1 lamin B1 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:23650370 733221 Lmnb1 lamin B1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22116031 733221 Lmnb1 lamin B1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:22116031 733221 Lmnb1 lamin B1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15232008 733221 Lmnb1 lamin B1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22116031 733221 Lmnb1 lamin B1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23650370 733221 Lmnb1 lamin B1 gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20141003 MGI PMID:22116031 733221 Lmnb1 lamin B1 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:23650370 733221 Lmnb1 lamin B1 gene MP:0012174 flat head IAGP N RGD:5509061 20141003 MGI PMID:23650370 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15936750 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15936750 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20231221 MGI PMID:15936750 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:14993236 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20150305 MGI PMID:25249606 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20150305 MGI PMID:25249606 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:14993236 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:12897135 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20150305 MGI PMID:25249606 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15936750 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0002748 abnormal pulmonary valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14993236 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0003434 decreased susceptibility to induced choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:18381816 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:12897135 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20150305 MGI PMID:25249606 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0009392 retina gliosis IAGP N RGD:5509061 20150305 MGI PMID:25249606 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:12897135 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:18381816 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20150305 MGI PMID:25249606 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0010235 abnormal retina inner limiting membrane morphology IAGP N RGD:5509061 20150305 MGI PMID:25249606 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15936750 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0010620 thick mitral valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0010620 thick mitral valve IAGP N RGD:5509061 20231221 MGI PMID:15936750 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0010629 thick tricuspid valve IAGP N RGD:5509061 20141003 MGI PMID:15936750 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0010629 thick tricuspid valve IAGP N RGD:5509061 20231221 MGI PMID:14993236 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15936750 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0031558 tricuspid valve hyperplasia IAGP N RGD:5509061 20240104 MGI PMID:15936750 733224 Adam15 ADAM metallopeptidase domain 15 gene MP:0031581 semilunar valve hyperplasia IAGP N RGD:5509061 20240125 MGI PMID:15936750 733229 Tbxa2r thromboxane A2 receptor gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:11964481 733229 Tbxa2r thromboxane A2 receptor gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12778172 733229 Tbxa2r thromboxane A2 receptor gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12778172 733229 Tbxa2r thromboxane A2 receptor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:9835625 733229 Tbxa2r thromboxane A2 receptor gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23624557 733229 Tbxa2r thromboxane A2 receptor gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:12778172 733229 Tbxa2r thromboxane A2 receptor gene MP:0002328 abnormal airway resistance IAGP N RGD:5509061 20141003 MGI PMID:21984570 733229 Tbxa2r thromboxane A2 receptor gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:12778172 733229 Tbxa2r thromboxane A2 receptor gene MP:0002351 abnormal cervical lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:12778172 733229 Tbxa2r thromboxane A2 receptor gene MP:0002531 abnormal type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:12778172 733229 Tbxa2r thromboxane A2 receptor gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:12778172 733229 Tbxa2r thromboxane A2 receptor gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:12778172 733229 Tbxa2r thromboxane A2 receptor gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:11964481 733229 Tbxa2r thromboxane A2 receptor gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23624557 733229 Tbxa2r thromboxane A2 receptor gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:9835625 733229 Tbxa2r thromboxane A2 receptor gene MP:0009548 abnormal platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:9835625 733229 Tbxa2r thromboxane A2 receptor gene MP:0009818 abnormal thromboxane level IAGP N RGD:5509061 20141003 MGI PMID:11964481 733232 Snd1 staphylococcal nuclease and tudor domain containing 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 733232 Snd1 staphylococcal nuclease and tudor domain containing 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 733232 Snd1 staphylococcal nuclease and tudor domain containing 1 gene MP:0000706 small thymus IEA N RGD:5509061 20220519 MGI 733232 Snd1 staphylococcal nuclease and tudor domain containing 1 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 733232 Snd1 staphylococcal nuclease and tudor domain containing 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20220519 MGI 733232 Snd1 staphylococcal nuclease and tudor domain containing 1 gene MP:0002637 small uterus IEA N RGD:5509061 20220519 MGI 733232 Snd1 staphylococcal nuclease and tudor domain containing 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 733232 Snd1 staphylococcal nuclease and tudor domain containing 1 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20211021 MGI 733232 Snd1 staphylococcal nuclease and tudor domain containing 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 733232 Snd1 staphylococcal nuclease and tudor domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 733232 Snd1 staphylococcal nuclease and tudor domain containing 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19801575 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15793246 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15793246 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15793246 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:15793246 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15793246 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15793246 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:15793246 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0005015 increased T cell number IEA N RGD:5509061 20181011 MGI 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15793246 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:15793246 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:15793246 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0008082 increased single-positive T cell number IEA N RGD:5509061 20181011 MGI 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20181011 MGI 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:15793246 733235 Dnajc3 DnaJ heat shock protein family (Hsp40) member C3 gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20181011 MGI 733237 Ostf1 osteoclast stimulating factor 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20180118 MGI PMID:28936620 733237 Ostf1 osteoclast stimulating factor 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 733237 Ostf1 osteoclast stimulating factor 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 733237 Ostf1 osteoclast stimulating factor 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 733237 Ostf1 osteoclast stimulating factor 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 733237 Ostf1 osteoclast stimulating factor 1 gene MP:0013615 increased volumetric bone mineral density IAGP N RGD:5509061 20180118 MGI PMID:28936620 733237 Ostf1 osteoclast stimulating factor 1 gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20180118 MGI PMID:28936620 733240 Pon1 paraoxonase 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9685159 733240 Pon1 paraoxonase 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:12633754 733240 Pon1 paraoxonase 1 gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9685159 733240 Pon1 paraoxonase 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:12633754 733240 Pon1 paraoxonase 1 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9685159 733240 Pon1 paraoxonase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:9685159 733240 Pon1 paraoxonase 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9685159 733242 Dnajc2 DnaJ heat shock protein family (Hsp40) member C2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20220811 MGI 733242 Dnajc2 DnaJ heat shock protein family (Hsp40) member C2 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 733242 Dnajc2 DnaJ heat shock protein family (Hsp40) member C2 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20240523 MGI 733242 Dnajc2 DnaJ heat shock protein family (Hsp40) member C2 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20201119 MGI PMID:31230751 733242 Dnajc2 DnaJ heat shock protein family (Hsp40) member C2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 733242 Dnajc2 DnaJ heat shock protein family (Hsp40) member C2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0000603 pale liver IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0001861 lung inflammation IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210520 MGI 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0008599 increased circulating interleukin-2 level IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0008602 increased circulating interleukin-4 level IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0013763 increased T-helper cell number IAGP N RGD:5509061 20170126 MGI PMID:27313209 733244 Pip4k2c phosphatidylinositol-5-phosphate 4-kinase, type II, gamma gene MP:0031301 chronic liver inflammation IAGP N RGD:5509061 20211028 MGI PMID:27313209 733248 S100a10 S100 calcium binding protein A10 (calpactin) gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:17035534 733248 S100a10 S100 calcium binding protein A10 (calpactin) gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:16400147 733248 S100a10 S100 calcium binding protein A10 (calpactin) gene MP:0003177 allodynia IAGP N RGD:5509061 20141003 MGI PMID:17035534 733248 S100a10 S100 calcium binding protein A10 (calpactin) gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:16400147 733248 S100a10 S100 calcium binding protein A10 (calpactin) gene MP:0003469 decreased single cell response intensity IAGP N RGD:5509061 20141003 MGI PMID:17035534 733248 S100a10 S100 calcium binding protein A10 (calpactin) gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:16400147 733248 S100a10 S100 calcium binding protein A10 (calpactin) gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:16400147 733248 S100a10 S100 calcium binding protein A10 (calpactin) gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16400147 733248 S100a10 S100 calcium binding protein A10 (calpactin) gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18256188 733251 Lrrc15 leucine rich repeat containing 15 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 733251 Lrrc15 leucine rich repeat containing 15 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20160421 MGI 733251 Lrrc15 leucine rich repeat containing 15 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20220811 MGI 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20181206 MGI PMID:16964445 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20181206 MGI PMID:16964445 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20181206 MGI PMID:16964445 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0001194 dermatitis IAGP N RGD:5509061 20181206 MGI PMID:16964445 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:8125254 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16872848 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20181206 MGI PMID:16964445 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20181206 MGI PMID:16964445 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20181206 MGI PMID:16964445 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8125254 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8125254 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:10547366 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10547366 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16872848 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20181206 MGI PMID:16964445 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20181206 MGI PMID:16964445 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20181206 MGI PMID:16964445 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0003073 abnormal metacarpal bone morphology IAGP N RGD:5509061 20181206 MGI PMID:16964445 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20181206 MGI PMID:16964445 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15067085 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0008559 abnormal interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16439675 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20181206 MGI PMID:16964445 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20181206 MGI PMID:16964445 733254 Fgr FGR proto-oncogene, Src family tyrosine kinase gene MP:0011514 skin hemorrhage IAGP N RGD:5509061 20181206 MGI PMID:16964445 733256 Dclre1c DNA cross-link repair 1C gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20150305 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:15699179 733256 Dclre1c DNA cross-link repair 1C gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19349461 733256 Dclre1c DNA cross-link repair 1C gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:12504013 733256 Dclre1c DNA cross-link repair 1C gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:15699179 733256 Dclre1c DNA cross-link repair 1C gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19349461 733256 Dclre1c DNA cross-link repair 1C gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19692705 733256 Dclre1c DNA cross-link repair 1C gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:24069355 733256 Dclre1c DNA cross-link repair 1C gene MP:0001260 increased body weight IEA N RGD:5509061 20181011 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0001262 decreased body weight IEA N RGD:5509061 20181011 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0001265 decreased body size IEA N RGD:5509061 20181011 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12504013 733256 Dclre1c DNA cross-link repair 1C gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15699179 733256 Dclre1c DNA cross-link repair 1C gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19349461 733256 Dclre1c DNA cross-link repair 1C gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19692705 733256 Dclre1c DNA cross-link repair 1C gene MP:0001806 decreased IgM level IEA N RGD:5509061 20150305 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12504013 733256 Dclre1c DNA cross-link repair 1C gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15699179 733256 Dclre1c DNA cross-link repair 1C gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18501428 733256 Dclre1c DNA cross-link repair 1C gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19692705 733256 Dclre1c DNA cross-link repair 1C gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:19349461 733256 Dclre1c DNA cross-link repair 1C gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18560421 733256 Dclre1c DNA cross-link repair 1C gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15699179 733256 Dclre1c DNA cross-link repair 1C gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:15699179 733256 Dclre1c DNA cross-link repair 1C gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15699179 733256 Dclre1c DNA cross-link repair 1C gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:24069355 733256 Dclre1c DNA cross-link repair 1C gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:19349461 733256 Dclre1c DNA cross-link repair 1C gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12504013 733256 Dclre1c DNA cross-link repair 1C gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:15699179 733256 Dclre1c DNA cross-link repair 1C gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:19692705 733256 Dclre1c DNA cross-link repair 1C gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:15699179 733256 Dclre1c DNA cross-link repair 1C gene MP:0004978 decreased B-1 B cell number IEA N RGD:5509061 20181011 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15699179 733256 Dclre1c DNA cross-link repair 1C gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19349461 733256 Dclre1c DNA cross-link repair 1C gene MP:0005018 decreased T cell number IEA N RGD:5509061 20150305 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19349461 733256 Dclre1c DNA cross-link repair 1C gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19692705 733256 Dclre1c DNA cross-link repair 1C gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:24069355 733256 Dclre1c DNA cross-link repair 1C gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15699179 733256 Dclre1c DNA cross-link repair 1C gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15699179 733256 Dclre1c DNA cross-link repair 1C gene MP:0005425 increased macrophage cell number IEA N RGD:5509061 20150305 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15699179 733256 Dclre1c DNA cross-link repair 1C gene MP:0006264 decreased systemic arterial systolic blood pressure IEA N RGD:5509061 20181011 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0008040 decreased NK T cell number IEA N RGD:5509061 20181011 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0008044 increased NK cell number IEA N RGD:5509061 20150305 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:24069355 733256 Dclre1c DNA cross-link repair 1C gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:19349461 733256 Dclre1c DNA cross-link repair 1C gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:24069355 733256 Dclre1c DNA cross-link repair 1C gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19349461 733256 Dclre1c DNA cross-link repair 1C gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19692705 733256 Dclre1c DNA cross-link repair 1C gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19349461 733256 Dclre1c DNA cross-link repair 1C gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19692705 733256 Dclre1c DNA cross-link repair 1C gene MP:0008083 decreased single-positive T cell number IEA N RGD:5509061 20150305 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:19349461 733256 Dclre1c DNA cross-link repair 1C gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:19349461 733256 Dclre1c DNA cross-link repair 1C gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:24069355 733256 Dclre1c DNA cross-link repair 1C gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:19692705 733256 Dclre1c DNA cross-link repair 1C gene MP:0008213 absent immature B cells IAGP N RGD:5509061 20141003 MGI PMID:12504013 733256 Dclre1c DNA cross-link repair 1C gene MP:0008213 absent immature B cells IAGP N RGD:5509061 20141003 MGI PMID:19692705 733256 Dclre1c DNA cross-link repair 1C gene MP:0008247 abnormal mononuclear cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19692705 733256 Dclre1c DNA cross-link repair 1C gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15699179 733256 Dclre1c DNA cross-link repair 1C gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:23207905 733256 Dclre1c DNA cross-link repair 1C gene MP:0008758 abnormal T cell receptor beta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:19349461 733256 Dclre1c DNA cross-link repair 1C gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:19349461 733256 Dclre1c DNA cross-link repair 1C gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:12504013 733256 Dclre1c DNA cross-link repair 1C gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:19692705 733256 Dclre1c DNA cross-link repair 1C gene MP:0010130 decreased DN1 thymic pro-T cell number IAGP N RGD:5509061 20141003 MGI PMID:24069355 733256 Dclre1c DNA cross-link repair 1C gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:24069355 733256 Dclre1c DNA cross-link repair 1C gene MP:0010250 absent thymus cortex IAGP N RGD:5509061 20141003 MGI PMID:15699179 733256 Dclre1c DNA cross-link repair 1C gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20150305 MGI 733256 Dclre1c DNA cross-link repair 1C gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20150305 MGI 733258 Itgb4 integrin beta 4 gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8707838 733258 Itgb4 integrin beta 4 gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9670011 733258 Itgb4 integrin beta 4 gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8673140 733258 Itgb4 integrin beta 4 gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:8673140 733258 Itgb4 integrin beta 4 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8673140 733258 Itgb4 integrin beta 4 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8707838 733258 Itgb4 integrin beta 4 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:18579745 733258 Itgb4 integrin beta 4 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:8673140 733258 Itgb4 integrin beta 4 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:8707838 733258 Itgb4 integrin beta 4 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:15731010 733258 Itgb4 integrin beta 4 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:18579745 733258 Itgb4 integrin beta 4 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:8707838 733258 Itgb4 integrin beta 4 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:9670011 733258 Itgb4 integrin beta 4 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9670011 733258 Itgb4 integrin beta 4 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:8707838 733258 Itgb4 integrin beta 4 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8707838 733258 Itgb4 integrin beta 4 gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20141003 MGI PMID:8707838 733258 Itgb4 integrin beta 4 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:8673140 733258 Itgb4 integrin beta 4 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:9670011 733258 Itgb4 integrin beta 4 gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:9670011 733258 Itgb4 integrin beta 4 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:8673140 733258 Itgb4 integrin beta 4 gene MP:0001849 ear inflammation IAGP N RGD:5509061 20141003 MGI PMID:15731010 733258 Itgb4 integrin beta 4 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:8707838 733258 Itgb4 integrin beta 4 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:9670011 733258 Itgb4 integrin beta 4 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15731010 733258 Itgb4 integrin beta 4 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8673140 733258 Itgb4 integrin beta 4 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:18579745 733258 Itgb4 integrin beta 4 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:18579745 733258 Itgb4 integrin beta 4 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:18579745 733258 Itgb4 integrin beta 4 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:18579745 733258 Itgb4 integrin beta 4 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:8707838 733258 Itgb4 integrin beta 4 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15542431 733258 Itgb4 integrin beta 4 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8673140 733258 Itgb4 integrin beta 4 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:18579745 733258 Itgb4 integrin beta 4 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:9670011 733258 Itgb4 integrin beta 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8673140 733258 Itgb4 integrin beta 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8707838 733258 Itgb4 integrin beta 4 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9670011 733258 Itgb4 integrin beta 4 gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20141003 MGI PMID:8673140 733258 Itgb4 integrin beta 4 gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20141003 MGI PMID:8707838 733258 Itgb4 integrin beta 4 gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20141003 MGI PMID:9670011 733258 Itgb4 integrin beta 4 gene MP:0030578 decreased keratinocyte adhesion IAGP N RGD:5509061 20180607 MGI PMID:9670011 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20160825 MGI PMID:27358191 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0001258 decreased body length IAGP N RGD:5509061 20160825 MGI PMID:27358191 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160825 MGI PMID:27358191 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20160825 MGI PMID:27358191 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0001921 reduced fertility IAGP N RGD:5509061 20160825 MGI PMID:27358191 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0001935 decreased litter size IAGP N RGD:5509061 20160825 MGI PMID:27358191 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0002176 increased brain weight IAGP N RGD:5509061 20160825 MGI PMID:27358191 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0002691 small stomach IAGP N RGD:5509061 20160825 MGI PMID:27358191 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0002717 abnormal male preputial gland morphology IAGP N RGD:5509061 20160825 MGI PMID:27358191 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0002833 increased heart weight IAGP N RGD:5509061 20160825 MGI PMID:27358191 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0003599 large penis IAGP N RGD:5509061 20160825 MGI PMID:27358191 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20160825 MGI PMID:27358191 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20160825 MGI PMID:27358191 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20220519 MGI 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20160825 MGI PMID:27358191 733259 Sgta small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20160825 MGI PMID:27358191 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0001934 increased litter size IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0003109 short femur IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20180719 MGI PMID:28581443 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0009299 decreased mesenteric fat pad weight IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0010964 increased compact bone volume IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0011019 abnormal adaptive thermogenesis IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20180719 MGI PMID:28581443 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20190627 MGI PMID:30413707 733262 Npffr2 neuropeptide FF receptor 2 gene MP:0011986 decreased macrophage proliferation IAGP N RGD:5509061 20180719 MGI PMID:28581443 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20180830 MGI PMID:28771483 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18326795 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10982764 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180830 MGI PMID:28771483 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:16877542 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0001258 decreased body length IAGP N RGD:5509061 20180830 MGI PMID:28771483 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11349005 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18326795 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180830 MGI PMID:28771483 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16816381 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16847341 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20180830 MGI PMID:28771483 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16847341 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16847341 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20180830 MGI PMID:28771483 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:14551238 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:7719350 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:7719350 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16877542 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:18596078 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19369559 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:16877542 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:7719350 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:7719350 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:7719350 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:7719350 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002493 increased IgG level IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:19234224 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180830 MGI PMID:28771483 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:16847341 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11349005 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20141003 MGI PMID:16877542 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002922 decreased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:16847341 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:16816381 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:18596078 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14718366 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20180830 MGI PMID:28771483 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210128 MGI 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:16816381 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0005238 increased brain size IAGP N RGD:5509061 20180830 MGI PMID:28771483 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20180830 MGI PMID:28771483 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:16877542 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0005525 increased renal plasma flow rate IAGP N RGD:5509061 20141003 MGI PMID:14718366 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0005526 decreased renal plasma flow rate IAGP N RGD:5509061 20141003 MGI PMID:18596078 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0005527 increased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:14718366 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0005530 decreased renal vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:14718366 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0005530 decreased renal vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:18596078 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180830 MGI PMID:28771483 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:14551238 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:14718366 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:18596078 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20180830 MGI PMID:28771483 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20180830 MGI PMID:28771483 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:16877542 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:11349005 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20190502 MGI PMID:27096368 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0010617 thick mitral valve cusps IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0010759 decreased right ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:18326795 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20180830 MGI PMID:28771483 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10982764 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0011470 increased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:14718366 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0011475 abnormal glycosaminoglycan level IAGP N RGD:5509061 20231109 MGI PMID:32655758 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0011741 increased urine nitrite level IAGP N RGD:5509061 20141003 MGI PMID:14718366 733265 Cybb cytochrome b-245, beta polypeptide gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20180830 MGI PMID:28771483 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16382159 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:22327219 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21300983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21300983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21048983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16382159 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22327219 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22327219 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:21048983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16382159 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16382159 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21048983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:21048983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16382159 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:22327219 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16382159 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21048983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21300983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21048983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22327219 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21048983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:22327219 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23799077 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:22327219 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21048983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21300983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:21048983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:21300983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21048983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:21300983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:21048983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21048983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:21300983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:21048983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:21048983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008556 abnormal tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16382159 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23799077 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008656 abnormal interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:16382159 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008662 abnormal interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:16382159 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16382159 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21048983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21300983 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 733266 Birc3 baculoviral IAP repeat-containing 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 733269 Chrnb3 cholinergic receptor, nicotinic, beta polypeptide 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:14657161 733269 Chrnb3 cholinergic receptor, nicotinic, beta polypeptide 3 gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20141003 MGI PMID:14657161 733272 S1pr5 sphingosine-1-phosphate receptor 5 gene MP:0005068 abnormal NK cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21911833 733272 S1pr5 sphingosine-1-phosphate receptor 5 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:21911833 733272 S1pr5 sphingosine-1-phosphate receptor 5 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19808259 733272 S1pr5 sphingosine-1-phosphate receptor 5 gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15703400 733272 S1pr5 sphingosine-1-phosphate receptor 5 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21911833 733274 Grb7 growth factor receptor bound protein 7 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20160421 MGI 733274 Grb7 growth factor receptor bound protein 7 gene MP:0003718 maternal effect IAGP N RGD:5509061 20240229 MGI PMID:38140940 733274 Grb7 growth factor receptor bound protein 7 gene MP:0008779 abnormal maternal behavior IAGP N RGD:5509061 20240229 MGI PMID:38140940 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18687666 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18687666 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:14701941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:20371632 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001123 dilated uterus IAGP N RGD:5509061 20141003 MGI PMID:8895659 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:14701941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001127 small ovary IAGP N RGD:5509061 20220602 MGI PMID:21248289 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:16513794 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16513794 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17609433 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18809571 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20160811 MGI PMID:26061565 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17142319 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:22791749 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001147 small testis IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:8895659 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:17142319 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:19237610 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:21860425 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:8895659 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17142319 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22791749 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18687666 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:19237610 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160204 MGI PMID:22331912 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20160204 MGI PMID:25815421 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:20371632 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18687666 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:17404209 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:20858757 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:17404209 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20371632 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001749 suppressed circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:19819941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001749 suppressed circulating follicle stimulating hormone level IAGP N RGD:5509061 20160811 MGI PMID:26061565 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:14701941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:18809571 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:20808952 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:14701941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:18809571 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17404209 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17404209 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:8895659 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:14701941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17404209 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17609433 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:18809571 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:20808952 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:20858757 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220602 MGI PMID:21248289 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:16513794 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17142319 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17967875 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21860425 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8895659 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14701941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17609433 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20220602 MGI PMID:21248289 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001930 abnormal meiosis IAGP N RGD:5509061 20141003 MGI PMID:17142319 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:14701941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:16513794 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17609433 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18687666 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18809571 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:20371632 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:20858757 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220602 MGI PMID:21248289 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:12368913 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:8895659 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:14701941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002016 ovary cyst IAGP N RGD:5509061 20160811 MGI PMID:26061565 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002016 ovary cyst IAGP N RGD:5509061 20220602 MGI PMID:21248289 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8895659 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:22331912 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:25815421 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18687666 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19819941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20371632 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002083 premature death IAGP N RGD:5509061 20160204 MGI PMID:22331912 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002083 premature death IAGP N RGD:5509061 20160204 MGI PMID:25815421 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002210 abnormal sex determination IAGP N RGD:5509061 20141003 MGI PMID:21490063 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17142319 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002676 uterus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20858757 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:14701941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002681 increased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:17609433 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:20371632 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20160811 MGI PMID:26061565 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:14701941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:17142319 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8895659 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:12368913 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:8895659 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:21860425 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:20858757 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:16513794 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003379 absent sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:17404209 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20220602 MGI PMID:21248289 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20141003 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20160204 MGI PMID:22331912 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17967875 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:22331912 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20160204 MGI PMID:25815421 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003582 abnormal ovary development IAGP N RGD:5509061 20141003 MGI PMID:20371632 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003700 abnormal oviduct transport IAGP N RGD:5509061 20141003 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003826 abnormal Mullerian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:21490063 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:17404209 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17404209 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20858757 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:20371632 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:17609433 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14701941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22791749 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004855 increased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:17609433 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:20371632 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:20858757 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:22791749 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20858757 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0005131 increased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17609433 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0005158 ovary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0005158 ovary hypoplasia IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:17142319 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20160811 MGI PMID:26061565 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:16513794 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0005324 ascites IAGP N RGD:5509061 20160204 MGI PMID:22331912 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0005324 ascites IAGP N RGD:5509061 20160204 MGI PMID:25815421 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20160811 MGI PMID:26061565 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:16513794 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:18809571 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:17967875 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17967875 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19237610 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21860425 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8895659 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0006418 abnormal testis cord formation IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17967875 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18687666 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20161222 MGI PMID:27354067 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:17404209 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:20858757 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008257 thin myometrium IAGP N RGD:5509061 20141003 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008257 thin myometrium IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:17142319 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17404209 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16513794 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:20808952 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20220609 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008876 decreased uterine NK cell number IAGP N RGD:5509061 20141003 MGI PMID:20858757 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:20808952 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:17967875 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009012 short diestrus IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009018 short estrus IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009069 dilated oviduct IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009071 short oviduct IAGP N RGD:5509061 20141003 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009089 short uterine horn IAGP N RGD:5509061 20141003 MGI PMID:17404209 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009089 short uterine horn IAGP N RGD:5509061 20141003 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20858757 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009094 abnormal endometrial gland morphology IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009096 decreased endometrial gland number IAGP N RGD:5509061 20141003 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009096 decreased endometrial gland number IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009139 failure of Mullerian duct regression IAGP N RGD:5509061 20141003 MGI PMID:21490063 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009207 internal male genitalia hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17609433 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009373 abnormal cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:16513794 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009373 abnormal cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:18809571 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009374 absent cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:16513794 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:17404209 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20141003 MGI PMID:17609433 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20141003 MGI PMID:15118069 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20220407 MGI PMID:17609433 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20220602 MGI PMID:21248289 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009592 increased Leydig cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8895659 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:18687666 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17404209 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20808952 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20808952 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:14701941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:16513794 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18809571 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18687666 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19237610 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19819941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21860425 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8895659 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20160204 MGI PMID:25815421 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20160811 MGI PMID:26061565 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20161222 MGI PMID:27354067 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0013399 endometrium fibrosis IAGP N RGD:5509061 20141218 MGI PMID:20858757 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0013400 abnormal endometrial gland development IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0013539 increased ovary adenoma incidence IAGP N RGD:5509061 20161222 MGI PMID:27354067 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0014515 decreased circulating anti-Mullerian hormone level IAGP N RGD:5509061 20240822 MGI PMID:21248289 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0020356 abnormal Sertoli cell barrier function IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220203 MGI PMID:21172404 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0021106 abnormal secondary ovarian follicle morphology IAGP N RGD:5509061 20220407 MGI PMID:16513794 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20191219 MGI PMID:17404209 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031018 decreased granulosa cell proliferation IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20200130 MGI PMID:18809571 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031080 pulmonary embolism IAGP N RGD:5509061 20200709 MGI PMID:18687666 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031137 vaginal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:17404209 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18809571 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20808952 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:22128018 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20808952 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220609 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031383 increased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:16513794 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031407 increased Sertoli cell proliferation IAGP N RGD:5509061 20220630 MGI PMID:22791749 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:14701941 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:18703422 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:18703631 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:21248289 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220630 MGI PMID:21248289 733277 Amhr2 anti-Mullerian hormone type 2 receptor gene MP:0031434 increased miscarriage rate IAGP N RGD:5509061 20220915 MGI PMID:17404209 733282 Slc22a4 solute carrier family 22 (organic cation transporter), member 4 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:20224991 733282 Slc22a4 solute carrier family 22 (organic cation transporter), member 4 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:20224991 733282 Slc22a4 solute carrier family 22 (organic cation transporter), member 4 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:20224991 733282 Slc22a4 solute carrier family 22 (organic cation transporter), member 4 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:20224991 733282 Slc22a4 solute carrier family 22 (organic cation transporter), member 4 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20181227 MGI 733282 Slc22a4 solute carrier family 22 (organic cation transporter), member 4 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20224991 733284 Alcam activated leukocyte cell adhesion molecule gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15345243 733284 Alcam activated leukocyte cell adhesion molecule gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:15345243 733284 Alcam activated leukocyte cell adhesion molecule gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:15345243 733284 Alcam activated leukocyte cell adhesion molecule gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15345243 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:24190965 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:24190965 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:24190965 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24190965 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:24190965 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:24190965 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:24190965 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:24190965 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:24190965 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:24190965 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:16449655 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:24190965 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16449655 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:24190965 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0010014 hippocampus pyramidal cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:24190965 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24190965 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16449655 733285 Ssb small RNA binding exonuclease protection factor La gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:24190965 733286 Ap3m2 adaptor-related protein complex 3, mu 2 subunit gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15492041 733286 Ap3m2 adaptor-related protein complex 3, mu 2 subunit gene MP:0000948 nonconvulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:15492041 733286 Ap3m2 adaptor-related protein complex 3, mu 2 subunit gene MP:0001499 abnormal kindling response IAGP N RGD:5509061 20141003 MGI PMID:15492041 733286 Ap3m2 adaptor-related protein complex 3, mu 2 subunit gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15492041 733286 Ap3m2 adaptor-related protein complex 3, mu 2 subunit gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15492041 733286 Ap3m2 adaptor-related protein complex 3, mu 2 subunit gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:15492041 733286 Ap3m2 adaptor-related protein complex 3, mu 2 subunit gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20211021 MGI 733286 Ap3m2 adaptor-related protein complex 3, mu 2 subunit gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:15492041 733286 Ap3m2 adaptor-related protein complex 3, mu 2 subunit gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:15492041 733286 Ap3m2 adaptor-related protein complex 3, mu 2 subunit gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15492041 733288 Chrna9 cholinergic receptor, nicotinic, alpha polypeptide 9 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:10402196 733288 Chrna9 cholinergic receptor, nicotinic, alpha polypeptide 9 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 733288 Chrna9 cholinergic receptor, nicotinic, alpha polypeptide 9 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19166271 733288 Chrna9 cholinergic receptor, nicotinic, alpha polypeptide 9 gene MP:0004415 abnormal cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:10402196 733288 Chrna9 cholinergic receptor, nicotinic, alpha polypeptide 9 gene MP:0004415 abnormal cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:14757515 733288 Chrna9 cholinergic receptor, nicotinic, alpha polypeptide 9 gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19166271 733288 Chrna9 cholinergic receptor, nicotinic, alpha polypeptide 9 gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18077337 733288 Chrna9 cholinergic receptor, nicotinic, alpha polypeptide 9 gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19166271 733288 Chrna9 cholinergic receptor, nicotinic, alpha polypeptide 9 gene MP:0004632 abnormal cochlear OHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:10402196 733288 Chrna9 cholinergic receptor, nicotinic, alpha polypeptide 9 gene MP:0004633 abnormal cochlear IHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:10402196 733288 Chrna9 cholinergic receptor, nicotinic, alpha polypeptide 9 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:10402196 733288 Chrna9 cholinergic receptor, nicotinic, alpha polypeptide 9 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:19166271 733288 Chrna9 cholinergic receptor, nicotinic, alpha polypeptide 9 gene MP:0004925 decreased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20141003 MGI PMID:19166271 733288 Chrna9 cholinergic receptor, nicotinic, alpha polypeptide 9 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:19166271 733290 Akr1c18 aldo-keto reductase family 1, member C18 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17272929 733290 Akr1c18 aldo-keto reductase family 1, member C18 gene MP:0002293 long gestation period IAGP N RGD:5509061 20141003 MGI PMID:15471942 733290 Akr1c18 aldo-keto reductase family 1, member C18 gene MP:0002293 long gestation period IAGP N RGD:5509061 20141003 MGI PMID:17272929 733290 Akr1c18 aldo-keto reductase family 1, member C18 gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:17272929 733290 Akr1c18 aldo-keto reductase family 1, member C18 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:17272929 733290 Akr1c18 aldo-keto reductase family 1, member C18 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:17272929 733290 Akr1c18 aldo-keto reductase family 1, member C18 gene MP:0012010 parturition failure IAGP N RGD:5509061 20141003 MGI PMID:15471942 733292 As3mt arsenite methyltransferase gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:19691357 733292 As3mt arsenite methyltransferase gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:19691357 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000075 absent neurocranium IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000099 absent vomer bone IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000101 absent ethmoid bone IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000105 impaired ossification of basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16917506 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000789 thickened cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000821 choroid plexus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000821 choroid plexus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000828 abnormal fourth ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000831 diencephalon hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000833 thalamus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000839 hypothalamus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000839 hypothalamus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000898 midbrain hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11504943 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18256270 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000919 cranioschisis IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000919 cranioschisis IAGP N RGD:5509061 20141003 MGI PMID:11504943 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000935 abnormal folding of telencephalic vesicles IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:18256270 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0001308 abnormal lens polarity IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0001329 retina hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12107826 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20150212 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11504943 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20120112 MGI 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18256270 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:18256270 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16917506 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15703386 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16917506 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18256270 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0004203 abnormal cranial flexure morphology IAGP N RGD:5509061 20171214 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0004327 increased vestibular hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15843406 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0004383 absent interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0004407 increased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:15843406 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0004419 absent parietal bone IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0004443 absent supraoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18256270 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0005297 spina bifida occulta IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:16917506 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0009264 failure of eyelid fusion IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0009889 persistence of medial edge epithelium during palatal shelf fusion IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0012174 flat head IAGP N RGD:5509061 20141003 MGI PMID:9753321 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0012260 encephalomeningocele IAGP N RGD:5509061 20141003 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0012702 increased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0013500 abnormal fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:10656767 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:9753320 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0030045 abnormal forehead shape IAGP N RGD:5509061 20170921 MGI PMID:9216040 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0030069 broad face IAGP N RGD:5509061 20170921 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0030251 broad frontonasal prominence IAGP N RGD:5509061 20171019 MGI PMID:23892366 733294 Apaf1 apoptotic peptidase activating factor 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:10656767 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20180426 MGI PMID:27721430 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20240502 MGI PMID:32814047 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180426 MGI PMID:27721430 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20180426 MGI PMID:27721430 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20180426 MGI PMID:27721430 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20181227 MGI 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20211021 MGI 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20180426 MGI PMID:27721430 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20210128 MGI 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20181227 MGI 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0010751 decreased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20180426 MGI PMID:27721430 733297 Usp15 ubiquitin specific peptidase 15 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210520 MGI 733301 Cd151 CD151 antigen gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:15199151 733301 Cd151 CD151 antigen gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:23792458 733301 Cd151 CD151 antigen gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:23792458 733301 Cd151 CD151 antigen gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:17023588 733301 Cd151 CD151 antigen gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:23792458 733301 Cd151 CD151 antigen gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20160623 MGI PMID:17023588 733301 Cd151 CD151 antigen gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17023588 733301 Cd151 CD151 antigen gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23792458 733301 Cd151 CD151 antigen gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15199151 733301 Cd151 CD151 antigen gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17023588 733301 Cd151 CD151 antigen gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:15199151 733301 Cd151 CD151 antigen gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0008138 absent podocyte foot process IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23792458 733301 Cd151 CD151 antigen gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0011454 abnormal glomerular endothelium fenestra morphology IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0011483 renal glomerular synechia IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0011483 renal glomerular synechia IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0011534 granular kidney IAGP N RGD:5509061 20141003 MGI PMID:17015618 733301 Cd151 CD151 antigen gene MP:0011534 granular kidney IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20141003 MGI PMID:18787104 733301 Cd151 CD151 antigen gene MP:0012193 increased keratinocyte migration IAGP N RGD:5509061 20141003 MGI PMID:23792458 733301 Cd151 CD151 antigen gene MP:0012194 decreased keratinocyte migration IAGP N RGD:5509061 20150205 MGI PMID:15199151 733304 Wnt2b wingless-type MMTV integration site family, member 2B gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 733304 Wnt2b wingless-type MMTV integration site family, member 2B gene MP:0000691 enlarged spleen IEA N RGD:5509061 20181227 MGI 733304 Wnt2b wingless-type MMTV integration site family, member 2B gene MP:0000692 small spleen IEA N RGD:5509061 20181227 MGI 733304 Wnt2b wingless-type MMTV integration site family, member 2B gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:19686689 733304 Wnt2b wingless-type MMTV integration site family, member 2B gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210128 MGI 733304 Wnt2b wingless-type MMTV integration site family, member 2B gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20210128 MGI 733304 Wnt2b wingless-type MMTV integration site family, member 2B gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 733304 Wnt2b wingless-type MMTV integration site family, member 2B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19686689 733304 Wnt2b wingless-type MMTV integration site family, member 2B gene MP:0003068 enlarged kidney IEA N RGD:5509061 20181227 MGI 733304 Wnt2b wingless-type MMTV integration site family, member 2B gene MP:0010885 absent trachea IAGP N RGD:5509061 20141003 MGI PMID:19686689 733307 Laptm5 lysosomal-associated protein transmembrane 5 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18619870 733307 Laptm5 lysosomal-associated protein transmembrane 5 gene MP:0002534 abnormal type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18619870 733307 Laptm5 lysosomal-associated protein transmembrane 5 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18619870 733307 Laptm5 lysosomal-associated protein transmembrane 5 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 733307 Laptm5 lysosomal-associated protein transmembrane 5 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:18619870 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:20417598 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:20417598 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20160310 MGI PMID:25189211 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20160310 MGI PMID:25189211 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0001714 absent trophoblast giant cells IAGP N RGD:5509061 20141003 MGI PMID:19090619 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20160310 MGI PMID:25189211 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20160310 MGI PMID:25189211 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:20417598 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:19090619 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20160310 MGI PMID:25189211 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20160310 MGI PMID:25189211 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19090619 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19090619 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:20417598 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20141003 MGI 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:20417598 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20160310 MGI PMID:25189211 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20160310 MGI PMID:25189211 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19090619 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20417598 733308 Senp2 SUMO/sentrin specific peptidase 2 gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:19090619 733309 Mpst mercaptopyruvate sulfurtransferase gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:23759691 733309 Mpst mercaptopyruvate sulfurtransferase gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23759691 733309 Mpst mercaptopyruvate sulfurtransferase gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:23759691 733309 Mpst mercaptopyruvate sulfurtransferase gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23759691 733309 Mpst mercaptopyruvate sulfurtransferase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23759691 733309 Mpst mercaptopyruvate sulfurtransferase gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23759691 733309 Mpst mercaptopyruvate sulfurtransferase gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23759691 733309 Mpst mercaptopyruvate sulfurtransferase gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:23759691 733313 Suox sulfite oxidase gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20240523 MGI 733320 Sphk1 sphingosine kinase 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 733320 Sphk1 sphingosine kinase 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 733320 Sphk1 sphingosine kinase 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17363629 733320 Sphk1 sphingosine kinase 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 733320 Sphk1 sphingosine kinase 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 733320 Sphk1 sphingosine kinase 1 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20026661 733320 Sphk1 sphingosine kinase 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 733320 Sphk1 sphingosine kinase 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20026661 733320 Sphk1 sphingosine kinase 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23995678 733320 Sphk1 sphingosine kinase 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 733320 Sphk1 sphingosine kinase 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 733320 Sphk1 sphingosine kinase 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17363629 733320 Sphk1 sphingosine kinase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15459201 733320 Sphk1 sphingosine kinase 1 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:20026661 733320 Sphk1 sphingosine kinase 1 gene MP:0002392 abnormal Peyer's patch T cell area morphology IAGP N RGD:5509061 20141003 MGI PMID:20026661 733320 Sphk1 sphingosine kinase 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 733320 Sphk1 sphingosine kinase 1 gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:17363629 733320 Sphk1 sphingosine kinase 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 733320 Sphk1 sphingosine kinase 1 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:23995678 733320 Sphk1 sphingosine kinase 1 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:20026661 733320 Sphk1 sphingosine kinase 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:17320845 733320 Sphk1 sphingosine kinase 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16223773 733320 Sphk1 sphingosine kinase 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17363629 733320 Sphk1 sphingosine kinase 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:20026661 733320 Sphk1 sphingosine kinase 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17363629 733320 Sphk1 sphingosine kinase 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20026661 733320 Sphk1 sphingosine kinase 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19808259 733320 Sphk1 sphingosine kinase 1 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19808259 733320 Sphk1 sphingosine kinase 1 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19808259 733320 Sphk1 sphingosine kinase 1 gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18305483 733320 Sphk1 sphingosine kinase 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18305483 733320 Sphk1 sphingosine kinase 1 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:18305483 733320 Sphk1 sphingosine kinase 1 gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:17363629 733320 Sphk1 sphingosine kinase 1 gene MP:0009339 decreased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:20026661 733320 Sphk1 sphingosine kinase 1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18305483 733320 Sphk1 sphingosine kinase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0012503 increased midbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16314531 733320 Sphk1 sphingosine kinase 1 gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:16314531 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0000453 absent mouth IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0004838 abnormal neural fold elevation formation IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0012138 decreased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0012263 decreased hindbrain size IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0012532 abnormal surface ectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0013180 truncated tail bud IAGP N RGD:5509061 20141003 MGI PMID:17954558 733324 Csnk2a1 casein kinase 2, alpha 1 polypeptide gene MP:0031587 abnormal pericardium development IAGP N RGD:5509061 20240229 MGI PMID:17954558 733326 Uxs1 UDP-glucuronate decarboxylase 1 gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20141003 MGI 733326 Uxs1 UDP-glucuronate decarboxylase 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:14775691 733326 Uxs1 UDP-glucuronate decarboxylase 1 gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:14775691 733326 Uxs1 UDP-glucuronate decarboxylase 1 gene MP:0008499 increased IgG1 level IEA N RGD:5509061 20141003 MGI 733326 Uxs1 UDP-glucuronate decarboxylase 1 gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 733327 Gpx6 glutathione peroxidase 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 733328 Cplx1 complexin 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:17692307 733328 Cplx1 complexin 1 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:11163241 733328 Cplx1 complexin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18577553 733328 Cplx1 complexin 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11163241 733328 Cplx1 complexin 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:18505837 733328 Cplx1 complexin 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:11163241 733328 Cplx1 complexin 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18577553 733328 Cplx1 complexin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11163241 733328 Cplx1 complexin 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11163241 733328 Cplx1 complexin 1 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:18577553 733328 Cplx1 complexin 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18577553 733328 Cplx1 complexin 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18505837 733328 Cplx1 complexin 1 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:17692307 733328 Cplx1 complexin 1 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:18577553 733328 Cplx1 complexin 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18505837 733328 Cplx1 complexin 1 gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:19553439 733328 Cplx1 complexin 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18505837 733328 Cplx1 complexin 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19553439 733328 Cplx1 complexin 1 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:18505837 733328 Cplx1 complexin 1 gene MP:0006335 abnormal hearing electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19553439 733328 Cplx1 complexin 1 gene MP:0010746 abnormal pre-Botzinger complex physiology IAGP N RGD:5509061 20141003 MGI PMID:18505837 733328 Cplx1 complexin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11163241 733328 Cplx1 complexin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18505837 733328 Cplx1 complexin 1 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:19553439 733328 Cplx1 complexin 1 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:18505837 733328 Cplx1 complexin 1 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:19553439 733328 Cplx1 complexin 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:19553439 733328 Cplx1 complexin 1 gene MP:0014372 decreased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:18505837 733328 Cplx1 complexin 1 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:18505837 733328 Cplx1 complexin 1 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:19553439 733328 Cplx1 complexin 1 gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:18505837 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:10470077 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17565006 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0000745 tremors IEA N RGD:5509061 20141003 MGI 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0002078 abnormal glucose homeostasis IEA N RGD:5509061 20160804 MGI 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20160804 MGI 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141218 MGI PMID:10470077 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17038639 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20160421 MGI 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0003062 abnormal coping response IEA N RGD:5509061 20160804 MGI 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:11956240 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10470077 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:10470077 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141218 MGI PMID:10470077 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20160804 MGI 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141218 MGI PMID:10470077 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10470077 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17565006 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0005015 increased T cell number IEA N RGD:5509061 20160804 MGI 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:17565006 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0005447 abnormal synaptic norepinephrine release IAGP N RGD:5509061 20141003 MGI PMID:17565006 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:11956240 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:10470077 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20200402 MGI 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10470077 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:11956240 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0008921 increased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:17565006 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:10470077 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:17565006 733330 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 gene MP:0011746 spleen fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10470077 733333 Pfn1 profilin 1 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:19262563 733333 Pfn1 profilin 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:19262563 733333 Pfn1 profilin 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20230601 MGI PMID:36599901 733333 Pfn1 profilin 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:19262563 733333 Pfn1 profilin 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10069337 733333 Pfn1 profilin 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:10069337 733333 Pfn1 profilin 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19262563 733333 Pfn1 profilin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19262563 733333 Pfn1 profilin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19262563 733333 Pfn1 profilin 1 gene MP:0001307 fused cornea and lens IEA N RGD:5509061 20150430 MGI 733333 Pfn1 profilin 1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20181227 MGI 733333 Pfn1 profilin 1 gene MP:0001314 cornea opacity IEA N RGD:5509061 20181227 MGI 733333 Pfn1 profilin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10069337 733333 Pfn1 profilin 1 gene MP:0001890 anencephaly IAGP N RGD:5509061 20141003 MGI PMID:10069337 733333 Pfn1 profilin 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:19262563 733333 Pfn1 profilin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:23000962 733333 Pfn1 profilin 1 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:23000962 733333 Pfn1 profilin 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:19262563 733333 Pfn1 profilin 1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20230601 MGI PMID:36599901 733333 Pfn1 profilin 1 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:19262563 733333 Pfn1 profilin 1 gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20160616 MGI PMID:23000962 733333 Pfn1 profilin 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:19262563 733333 Pfn1 profilin 1 gene MP:0003707 increased cell nucleus count IAGP N RGD:5509061 20230601 MGI PMID:36599901 733333 Pfn1 profilin 1 gene MP:0003708 binucleate IAGP N RGD:5509061 20230601 MGI PMID:36599901 733333 Pfn1 profilin 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17615372 733333 Pfn1 profilin 1 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:19262563 733333 Pfn1 profilin 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:19262563 733333 Pfn1 profilin 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:23000962 733333 Pfn1 profilin 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 733333 Pfn1 profilin 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17615372 733333 Pfn1 profilin 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:23000962 733333 Pfn1 profilin 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19262563 733333 Pfn1 profilin 1 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20150430 MGI 733333 Pfn1 profilin 1 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20171221 MGI PMID:19262563 733333 Pfn1 profilin 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20141003 MGI 733333 Pfn1 profilin 1 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20141003 MGI 733333 Pfn1 profilin 1 gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20210128 MGI 733333 Pfn1 profilin 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160804 MGI 733333 Pfn1 profilin 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19262563 733333 Pfn1 profilin 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10069337 733333 Pfn1 profilin 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11274401 733333 Pfn1 profilin 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11274401 733333 Pfn1 profilin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733333 Pfn1 profilin 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11274401 733333 Pfn1 profilin 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17615372 733333 Pfn1 profilin 1 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17049405 733333 Pfn1 profilin 1 gene MP:0013289 abnormal mitotic cytokinesis IAGP N RGD:5509061 20230601 MGI PMID:36599901 733333 Pfn1 profilin 1 gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:19262563 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19450521 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:23188715 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200123 MGI PMID:31285329 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200123 MGI PMID:31285329 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20200123 MGI PMID:31285329 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:23188715 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19450521 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20200123 MGI PMID:31285329 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:19450521 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:19450521 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20200123 MGI PMID:31285329 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200123 MGI PMID:31285329 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:23188715 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20200123 MGI PMID:31285329 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20200123 MGI PMID:31285329 733335 Trpc5 transient receptor potential cation channel, subfamily C, member 5 gene MP:0009016 abnormal estrus IAGP N RGD:5509061 20200123 MGI PMID:31285329 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:19548314 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20230727 MGI PMID:33359667 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20170223 MGI PMID:24717294 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:21109326 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20230727 MGI PMID:33359667 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:21109326 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21109326 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230727 MGI PMID:33359667 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19548314 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21109326 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20230727 MGI PMID:33359667 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19548314 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20230727 MGI PMID:33359667 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:19548314 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20170223 MGI PMID:24717294 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:21109326 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20230727 MGI PMID:33359667 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20170223 MGI PMID:24717294 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20170223 MGI PMID:24717294 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002959 increased urine microalbumin level IAGP N RGD:5509061 20170223 MGI PMID:24717294 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19548314 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:21109326 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20170223 MGI PMID:24717294 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20230727 MGI PMID:33359667 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21109326 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:19548314 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20170223 MGI PMID:24717294 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19548314 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21109326 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20230727 MGI PMID:33359667 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20230727 MGI PMID:33359667 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20170223 MGI PMID:24717294 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20230727 MGI PMID:33359667 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:19548314 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:21109326 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20170223 MGI PMID:24717294 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20230727 MGI PMID:33359667 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20230727 MGI PMID:33359667 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20170223 MGI PMID:24717294 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21109326 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20230727 MGI PMID:33359667 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20230727 MGI PMID:33359667 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19548314 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21109326 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20170223 MGI PMID:24717294 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0009810 increased urine uric acid level IAGP N RGD:5509061 20170223 MGI PMID:24717294 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:21109326 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20200130 MGI PMID:19548314 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20200130 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20230727 MGI PMID:33359667 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20141003 MGI PMID:8640227 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0011435 increased urine magnesium level IAGP N RGD:5509061 20170223 MGI PMID:24717294 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0031003 increased kidney glycogen level IAGP N RGD:5509061 20200130 MGI PMID:19548314 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0031003 increased kidney glycogen level IAGP N RGD:5509061 20200130 MGI PMID:24717294 733336 G6pc1 glucose-6-phosphatase catalytic subunit 1 gene MP:0031003 increased kidney glycogen level IAGP N RGD:5509061 20200130 MGI PMID:8640227 733338 Stip1 stress-induced phosphoprotein 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23729591 733338 Stip1 stress-induced phosphoprotein 1 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:23729591 733338 Stip1 stress-induced phosphoprotein 1 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:23729591 733338 Stip1 stress-induced phosphoprotein 1 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:23729591 733338 Stip1 stress-induced phosphoprotein 1 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:23729591 733338 Stip1 stress-induced phosphoprotein 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:23729591 733338 Stip1 stress-induced phosphoprotein 1 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23729591 733338 Stip1 stress-induced phosphoprotein 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23729591 733338 Stip1 stress-induced phosphoprotein 1 gene MP:0010038 abnormal placenta physiology IAGP N RGD:5509061 20141003 MGI PMID:23729591 733338 Stip1 stress-induced phosphoprotein 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:23729591 733338 Stip1 stress-induced phosphoprotein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23729591 733338 Stip1 stress-induced phosphoprotein 1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23729591 733338 Stip1 stress-induced phosphoprotein 1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:23729591 733338 Stip1 stress-induced phosphoprotein 1 gene MP:0012556 increased cell death IAGP N RGD:5509061 20141003 MGI PMID:23729591 733338 Stip1 stress-induced phosphoprotein 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:23729591 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0000160 kyphosis IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0001263 weight loss IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0002083 premature death IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0011939 increased food intake IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0011969 abnormal circulating triglyceride level IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0020521 browned white adipose tissue morphology IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0030753 decreased choline level IAGP N RGD:5509061 20230316 MGI PMID:36719796 733340 Pnpla7 patatin-like phospholipase domain containing 7 gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20230316 MGI PMID:36719796 733343 Serpinb10 serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 10 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20231207 MGI 733343 Serpinb10 serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 10 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 733343 Serpinb10 serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 10 gene MP:0000277 abnormal heart shape IEA N RGD:5509061 20210826 MGI 733343 Serpinb10 serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 10 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 733343 Serpinb10 serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 10 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 733343 Serpinb10 serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 10 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 733343 Serpinb10 serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 10 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 733343 Serpinb10 serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 10 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20210520 MGI 733343 Serpinb10 serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 10 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 733343 Serpinb10 serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 10 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 733343 Serpinb10 serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 10 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 733343 Serpinb10 serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 10 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20240523 MGI 733343 Serpinb10 serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 10 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 733346 Rimbp2 RIMS binding protein 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 733346 Rimbp2 RIMS binding protein 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20180308 MGI PMID:27671655 733346 Rimbp2 RIMS binding protein 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20180308 MGI PMID:27671655 733346 Rimbp2 RIMS binding protein 2 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20180308 MGI PMID:27671655 733346 Rimbp2 RIMS binding protein 2 gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20180308 MGI PMID:27671655 733346 Rimbp2 RIMS binding protein 2 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20180308 MGI PMID:27671655 733346 Rimbp2 RIMS binding protein 2 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20180308 MGI PMID:27671655 733346 Rimbp2 RIMS binding protein 2 gene MP:0014254 increased paired-pulse ratio IAGP N RGD:5509061 20230706 MGI PMID:27671655 733349 A1cf APOBEC1 complementation factor gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20160616 MGI PMID:22375032 733349 A1cf APOBEC1 complementation factor gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20171026 MGI PMID:27548259 733349 A1cf APOBEC1 complementation factor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20160616 MGI PMID:19028670 733349 A1cf APOBEC1 complementation factor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20160616 MGI PMID:19328205 733349 A1cf APOBEC1 complementation factor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170810 MGI PMID:26356605 733349 A1cf APOBEC1 complementation factor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170831 MGI PMID:19850880 733349 A1cf APOBEC1 complementation factor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20171026 MGI PMID:27548259 733349 A1cf APOBEC1 complementation factor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20180920 MGI PMID:26891723 733349 A1cf APOBEC1 complementation factor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20200206 MGI PMID:31209364 733349 A1cf APOBEC1 complementation factor gene MP:0000274 enlarged heart IAGP N RGD:5509061 20240307 MGI PMID:35803927 733349 A1cf APOBEC1 complementation factor gene MP:0000277 abnormal heart shape IAGP N RGD:5509061 20160616 MGI PMID:15662031 733349 A1cf APOBEC1 complementation factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20160616 MGI PMID:15662031 733349 A1cf APOBEC1 complementation factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20160616 MGI PMID:16260633 733349 A1cf APOBEC1 complementation factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20160616 MGI PMID:17823658 733349 A1cf APOBEC1 complementation factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20160616 MGI PMID:22375032 733349 A1cf APOBEC1 complementation factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20160616 MGI PMID:24840128 733349 A1cf APOBEC1 complementation factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20160721 MGI PMID:26119742 733349 A1cf APOBEC1 complementation factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20160929 MGI PMID:25787764 733349 A1cf APOBEC1 complementation factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170810 MGI PMID:17190866 733349 A1cf APOBEC1 complementation factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170831 MGI PMID:19850880 733349 A1cf APOBEC1 complementation factor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20240502 MGI PMID:38224947 733349 A1cf APOBEC1 complementation factor gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20171026 MGI PMID:27548259 733349 A1cf APOBEC1 complementation factor gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20200206 MGI PMID:31209364 733349 A1cf APOBEC1 complementation factor gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20230914 MGI PMID:37233188 733349 A1cf APOBEC1 complementation factor gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20160616 MGI PMID:19038262 733349 A1cf APOBEC1 complementation factor gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20160616 MGI PMID:23948483 733349 A1cf APOBEC1 complementation factor gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20160616 MGI PMID:24132636 733349 A1cf APOBEC1 complementation factor gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20160929 MGI PMID:25787764 733349 A1cf APOBEC1 complementation factor gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20240418 MGI PMID:34831084 733349 A1cf APOBEC1 complementation factor gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16055734 733349 A1cf APOBEC1 complementation factor gene MP:0001263 weight loss IAGP N RGD:5509061 20160616 MGI PMID:19376970 733349 A1cf APOBEC1 complementation factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20171116 MGI PMID:27184846 733349 A1cf APOBEC1 complementation factor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20160616 MGI PMID:15662031 733349 A1cf APOBEC1 complementation factor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20160616 MGI PMID:17334357 733349 A1cf APOBEC1 complementation factor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20160616 MGI PMID:17823658 733349 A1cf APOBEC1 complementation factor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20160616 MGI PMID:19028670 733349 A1cf APOBEC1 complementation factor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20160616 MGI PMID:19328205 733349 A1cf APOBEC1 complementation factor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20160616 MGI PMID:22375032 733349 A1cf APOBEC1 complementation factor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20170810 MGI PMID:26356605 733349 A1cf APOBEC1 complementation factor gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20200206 MGI PMID:31209364 733349 A1cf APOBEC1 complementation factor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20160616 MGI PMID:16260633 733349 A1cf APOBEC1 complementation factor gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20160616 MGI PMID:24840128 733349 A1cf APOBEC1 complementation factor gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20181018 MGI PMID:24658400 733349 A1cf APOBEC1 complementation factor gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20220811 MGI PMID:35358843 733349 A1cf APOBEC1 complementation factor gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20160616 MGI PMID:15662031 733349 A1cf APOBEC1 complementation factor gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20160616 MGI PMID:17823658 733349 A1cf APOBEC1 complementation factor gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20220811 MGI PMID:35358843 733349 A1cf APOBEC1 complementation factor gene MP:0001853 heart inflammation IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0001853 heart inflammation IAGP N RGD:5509061 20170810 MGI PMID:17190866 733349 A1cf APOBEC1 complementation factor gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20160616 MGI PMID:22869620 733349 A1cf APOBEC1 complementation factor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20160616 MGI PMID:23948483 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20160616 MGI PMID:15662031 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20160616 MGI PMID:16260633 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20160616 MGI PMID:17823658 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20160616 MGI PMID:19028670 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20160616 MGI PMID:19520971 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20160616 MGI PMID:21220308 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20160616 MGI PMID:21521762 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20160616 MGI PMID:21665954 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20160616 MGI PMID:22869620 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20160616 MGI PMID:24743769 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20160616 MGI PMID:24840128 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20170810 MGI PMID:26356605 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20170831 MGI PMID:19850880 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20171026 MGI PMID:27548259 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20180503 MGI PMID:29438013 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20200206 MGI PMID:31209364 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20220811 MGI PMID:35358843 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20230914 MGI PMID:37233188 733349 A1cf APOBEC1 complementation factor gene MP:0002083 premature death IAGP N RGD:5509061 20240307 MGI PMID:35803927 733349 A1cf APOBEC1 complementation factor gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20160616 MGI PMID:15662031 733349 A1cf APOBEC1 complementation factor gene MP:0002139 abnormal hepatobiliary system physiology IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160616 MGI PMID:23077570 733349 A1cf APOBEC1 complementation factor gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20160616 MGI PMID:24812305 733349 A1cf APOBEC1 complementation factor gene MP:0002626 increased heart rate IAGP N RGD:5509061 20160616 MGI PMID:15662031 733349 A1cf APOBEC1 complementation factor gene MP:0002626 increased heart rate IAGP N RGD:5509061 20160616 MGI PMID:22869620 733349 A1cf APOBEC1 complementation factor gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20160616 MGI PMID:15662031 733349 A1cf APOBEC1 complementation factor gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20160616 MGI PMID:17450150 733349 A1cf APOBEC1 complementation factor gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20160616 MGI PMID:17823658 733349 A1cf APOBEC1 complementation factor gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20160616 MGI PMID:19028670 733349 A1cf APOBEC1 complementation factor gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20160616 MGI PMID:19376970 733349 A1cf APOBEC1 complementation factor gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20220811 MGI PMID:35358843 733349 A1cf APOBEC1 complementation factor gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20230914 MGI PMID:37233188 733349 A1cf APOBEC1 complementation factor gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20160616 MGI PMID:15662031 733349 A1cf APOBEC1 complementation factor gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20160616 MGI PMID:19028670 733349 A1cf APOBEC1 complementation factor gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20230914 MGI PMID:37233188 733349 A1cf APOBEC1 complementation factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20160616 MGI PMID:16260633 733349 A1cf APOBEC1 complementation factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20160616 MGI PMID:17823658 733349 A1cf APOBEC1 complementation factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20160616 MGI PMID:19028670 733349 A1cf APOBEC1 complementation factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20160616 MGI PMID:19520971 733349 A1cf APOBEC1 complementation factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20160616 MGI PMID:22421363 733349 A1cf APOBEC1 complementation factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170810 MGI PMID:17190866 733349 A1cf APOBEC1 complementation factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170810 MGI PMID:26356605 733349 A1cf APOBEC1 complementation factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170831 MGI PMID:19850880 733349 A1cf APOBEC1 complementation factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20171026 MGI PMID:27548259 733349 A1cf APOBEC1 complementation factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20200206 MGI PMID:31209364 733349 A1cf APOBEC1 complementation factor gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20230914 MGI PMID:37233188 733349 A1cf APOBEC1 complementation factor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20160616 MGI PMID:17450150 733349 A1cf APOBEC1 complementation factor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20160616 MGI PMID:22375032 733349 A1cf APOBEC1 complementation factor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20160616 MGI PMID:24840128 733349 A1cf APOBEC1 complementation factor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20160929 MGI PMID:25787764 733349 A1cf APOBEC1 complementation factor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20180920 MGI PMID:26891723 733349 A1cf APOBEC1 complementation factor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20181018 MGI PMID:24658400 733349 A1cf APOBEC1 complementation factor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20220811 MGI PMID:35358843 733349 A1cf APOBEC1 complementation factor gene MP:0002833 increased heart weight IAGP N RGD:5509061 20220915 MGI PMID:35907876 733349 A1cf APOBEC1 complementation factor gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20160616 MGI PMID:19597047 733349 A1cf APOBEC1 complementation factor gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20160616 MGI PMID:19597047 733349 A1cf APOBEC1 complementation factor gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20160616 MGI PMID:17450150 733349 A1cf APOBEC1 complementation factor gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20240418 MGI PMID:34831084 733349 A1cf APOBEC1 complementation factor gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20240620 MGI PMID:35680100 733349 A1cf APOBEC1 complementation factor gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20160616 MGI PMID:19038262 733349 A1cf APOBEC1 complementation factor gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20160616 MGI PMID:24132636 733349 A1cf APOBEC1 complementation factor gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20160721 MGI PMID:26119742 733349 A1cf APOBEC1 complementation factor gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20240620 MGI PMID:35680100 733349 A1cf APOBEC1 complementation factor gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20160721 MGI PMID:26119742 733349 A1cf APOBEC1 complementation factor gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20160616 MGI PMID:15662031 733349 A1cf APOBEC1 complementation factor gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20160616 MGI PMID:21220308 733349 A1cf APOBEC1 complementation factor gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20160616 MGI PMID:15662031 733349 A1cf APOBEC1 complementation factor gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20160616 MGI PMID:19328205 733349 A1cf APOBEC1 complementation factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20160616 MGI PMID:16260633 733349 A1cf APOBEC1 complementation factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20160616 MGI PMID:22375032 733349 A1cf APOBEC1 complementation factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20160616 MGI PMID:22829020 733349 A1cf APOBEC1 complementation factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20160616 MGI PMID:24200690 733349 A1cf APOBEC1 complementation factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20170831 MGI PMID:19850880 733349 A1cf APOBEC1 complementation factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20180920 MGI PMID:26891723 733349 A1cf APOBEC1 complementation factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200206 MGI PMID:31209364 733349 A1cf APOBEC1 complementation factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20220811 MGI PMID:35358843 733349 A1cf APOBEC1 complementation factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20230914 MGI PMID:37233188 733349 A1cf APOBEC1 complementation factor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20240314 MGI PMID:36108935 733349 A1cf APOBEC1 complementation factor gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20160616 MGI PMID:24812305 733349 A1cf APOBEC1 complementation factor gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20170831 MGI PMID:19850880 733349 A1cf APOBEC1 complementation factor gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20171026 MGI PMID:27548259 733349 A1cf APOBEC1 complementation factor gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20160721 MGI PMID:26119742 733349 A1cf APOBEC1 complementation factor gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20160929 MGI PMID:25787764 733349 A1cf APOBEC1 complementation factor gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20160616 MGI PMID:15662031 733349 A1cf APOBEC1 complementation factor gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20160616 MGI PMID:19328205 733349 A1cf APOBEC1 complementation factor gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20160616 MGI PMID:22375032 733349 A1cf APOBEC1 complementation factor gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20160616 MGI PMID:22869620 733349 A1cf APOBEC1 complementation factor gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20181018 MGI PMID:24658400 733349 A1cf APOBEC1 complementation factor gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200206 MGI PMID:31209364 733349 A1cf APOBEC1 complementation factor gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20160616 MGI PMID:22375032 733349 A1cf APOBEC1 complementation factor gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20160616 MGI PMID:17823658 733349 A1cf APOBEC1 complementation factor gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20160616 MGI PMID:18794341 733349 A1cf APOBEC1 complementation factor gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20160616 MGI PMID:22992950 733349 A1cf APOBEC1 complementation factor gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20220811 MGI PMID:35358843 733349 A1cf APOBEC1 complementation factor gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20160616 MGI PMID:24812305 733349 A1cf APOBEC1 complementation factor gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20160616 MGI PMID:22829020 733349 A1cf APOBEC1 complementation factor gene MP:0003923 abnormal heart left atrium morphology IAGP N RGD:5509061 20160616 MGI PMID:19328205 733349 A1cf APOBEC1 complementation factor gene MP:0003928 increased heart rate variability IAGP N RGD:5509061 20160616 MGI PMID:18794341 733349 A1cf APOBEC1 complementation factor gene MP:0004011 decreased diastolic filling velocity IAGP N RGD:5509061 20160616 MGI PMID:17823658 733349 A1cf APOBEC1 complementation factor gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20160616 MGI PMID:16260633 733349 A1cf APOBEC1 complementation factor gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20160616 MGI PMID:17823658 733349 A1cf APOBEC1 complementation factor gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20160616 MGI PMID:22375032 733349 A1cf APOBEC1 complementation factor gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20170810 MGI PMID:17190866 733349 A1cf APOBEC1 complementation factor gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20170831 MGI PMID:19850880 733349 A1cf APOBEC1 complementation factor gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20181018 MGI PMID:24658400 733349 A1cf APOBEC1 complementation factor gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20220811 MGI PMID:35358843 733349 A1cf APOBEC1 complementation factor gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20220915 MGI PMID:35907876 733349 A1cf APOBEC1 complementation factor gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20160616 MGI PMID:16260633 733349 A1cf APOBEC1 complementation factor gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20170810 MGI PMID:17190866 733349 A1cf APOBEC1 complementation factor gene MP:0004093 diffuse Z line IAGP N RGD:5509061 20180531 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0004093 diffuse Z line IAGP N RGD:5509061 20220915 MGI PMID:35907876 733349 A1cf APOBEC1 complementation factor gene MP:0004114 abnormal atrioventricular node morphology IAGP N RGD:5509061 20160616 MGI PMID:18794341 733349 A1cf APOBEC1 complementation factor gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20170810 MGI PMID:17190866 733349 A1cf APOBEC1 complementation factor gene MP:0004122 abnormal sinus arrhythmia IAGP N RGD:5509061 20160616 MGI PMID:22869620 733349 A1cf APOBEC1 complementation factor gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20160616 MGI PMID:21665954 733349 A1cf APOBEC1 complementation factor gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20160616 MGI PMID:17450150 733349 A1cf APOBEC1 complementation factor gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20160616 MGI PMID:19328205 733349 A1cf APOBEC1 complementation factor gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20160616 MGI PMID:19597047 733349 A1cf APOBEC1 complementation factor gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20160616 MGI PMID:24132636 733349 A1cf APOBEC1 complementation factor gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20160721 MGI PMID:26119742 733349 A1cf APOBEC1 complementation factor gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20160929 MGI PMID:25787764 733349 A1cf APOBEC1 complementation factor gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20181018 MGI PMID:24658400 733349 A1cf APOBEC1 complementation factor gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20160616 MGI PMID:17916779 733349 A1cf APOBEC1 complementation factor gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20160616 MGI PMID:22829020 733349 A1cf APOBEC1 complementation factor gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20240418 MGI PMID:34831084 733349 A1cf APOBEC1 complementation factor gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20160616 MGI PMID:23540699 733349 A1cf APOBEC1 complementation factor gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20180920 MGI PMID:26891723 733349 A1cf APOBEC1 complementation factor gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20240502 MGI PMID:38224947 733349 A1cf APOBEC1 complementation factor gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20240530 MGI PMID:32805187 733349 A1cf APOBEC1 complementation factor gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20160616 MGI PMID:17450150 733349 A1cf APOBEC1 complementation factor gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20160616 MGI PMID:17823658 733349 A1cf APOBEC1 complementation factor gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20160616 MGI PMID:19376970 733349 A1cf APOBEC1 complementation factor gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20160616 MGI PMID:22829020 733349 A1cf APOBEC1 complementation factor gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20160616 MGI PMID:24812305 733349 A1cf APOBEC1 complementation factor gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20160616 MGI PMID:24840128 733349 A1cf APOBEC1 complementation factor gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20180920 MGI PMID:26891723 733349 A1cf APOBEC1 complementation factor gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20220811 MGI PMID:35358843 733349 A1cf APOBEC1 complementation factor gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20220915 MGI PMID:35907876 733349 A1cf APOBEC1 complementation factor gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20160929 MGI PMID:25787764 733349 A1cf APOBEC1 complementation factor gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20170831 MGI PMID:19850880 733349 A1cf APOBEC1 complementation factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160616 MGI PMID:17823658 733349 A1cf APOBEC1 complementation factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160616 MGI PMID:19328205 733349 A1cf APOBEC1 complementation factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160616 MGI PMID:19520971 733349 A1cf APOBEC1 complementation factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160616 MGI PMID:19597047 733349 A1cf APOBEC1 complementation factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160616 MGI PMID:21521762 733349 A1cf APOBEC1 complementation factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160616 MGI PMID:22375032 733349 A1cf APOBEC1 complementation factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170810 MGI PMID:26356605 733349 A1cf APOBEC1 complementation factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170831 MGI PMID:19850880 733349 A1cf APOBEC1 complementation factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20171026 MGI PMID:27548259 733349 A1cf APOBEC1 complementation factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20180503 MGI PMID:29438013 733349 A1cf APOBEC1 complementation factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20180920 MGI PMID:26891723 733349 A1cf APOBEC1 complementation factor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20240314 MGI PMID:36108935 733349 A1cf APOBEC1 complementation factor gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20160616 MGI PMID:24200690 733349 A1cf APOBEC1 complementation factor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0005202 lethargy IAGP N RGD:5509061 20160616 MGI PMID:22869620 733349 A1cf APOBEC1 complementation factor gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20210603 MGI PMID:33571905 733349 A1cf APOBEC1 complementation factor gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20160616 MGI PMID:23948483 733349 A1cf APOBEC1 complementation factor gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20170810 MGI PMID:26356605 733349 A1cf APOBEC1 complementation factor gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20170831 MGI PMID:19850880 733349 A1cf APOBEC1 complementation factor gene MP:0005324 ascites IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0005324 ascites IAGP N RGD:5509061 20170810 MGI PMID:17190866 733349 A1cf APOBEC1 complementation factor gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20160616 MGI PMID:16260633 733349 A1cf APOBEC1 complementation factor gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20160616 MGI PMID:19520971 733349 A1cf APOBEC1 complementation factor gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20160616 MGI PMID:22375032 733349 A1cf APOBEC1 complementation factor gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20160616 MGI PMID:22869620 733349 A1cf APOBEC1 complementation factor gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20160616 MGI PMID:24200690 733349 A1cf APOBEC1 complementation factor gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20181018 MGI PMID:24658400 733349 A1cf APOBEC1 complementation factor gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20240314 MGI PMID:36108935 733349 A1cf APOBEC1 complementation factor gene MP:0005331 insulin resistance IAGP N RGD:5509061 20240314 MGI PMID:36108935 733349 A1cf APOBEC1 complementation factor gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20160616 MGI PMID:15662031 733349 A1cf APOBEC1 complementation factor gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20160616 MGI PMID:19328205 733349 A1cf APOBEC1 complementation factor gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20160616 MGI PMID:19376970 733349 A1cf APOBEC1 complementation factor gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20160616 MGI PMID:21220308 733349 A1cf APOBEC1 complementation factor gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20160616 MGI PMID:22869620 733349 A1cf APOBEC1 complementation factor gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20160616 MGI PMID:24743769 733349 A1cf APOBEC1 complementation factor gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20160616 MGI PMID:24812305 733349 A1cf APOBEC1 complementation factor gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20220811 MGI PMID:35358843 733349 A1cf APOBEC1 complementation factor gene MP:0005378 growth/size/body region phenotype IAGP N RGD:5509061 20210429 MGI PMID:27956576 733349 A1cf APOBEC1 complementation factor gene MP:0005385 cardiovascular system phenotype IAGP N RGD:5509061 20210429 MGI PMID:27956576 733349 A1cf APOBEC1 complementation factor gene MP:0005389 reproductive system phenotype IAGP N RGD:5509061 20210429 MGI PMID:27956576 733349 A1cf APOBEC1 complementation factor gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20160616 MGI PMID:17334357 733349 A1cf APOBEC1 complementation factor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 733349 A1cf APOBEC1 complementation factor gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20160616 MGI PMID:22829020 733349 A1cf APOBEC1 complementation factor gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20160721 MGI PMID:26119742 733349 A1cf APOBEC1 complementation factor gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20220811 MGI PMID:35358843 733349 A1cf APOBEC1 complementation factor gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20220915 MGI PMID:35907876 733349 A1cf APOBEC1 complementation factor gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20230914 MGI PMID:37233188 733349 A1cf APOBEC1 complementation factor gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20160616 MGI PMID:24200690 733349 A1cf APOBEC1 complementation factor gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20160616 MGI PMID:17334357 733349 A1cf APOBEC1 complementation factor gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20160616 MGI PMID:17823658 733349 A1cf APOBEC1 complementation factor gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20160616 MGI PMID:22829020 733349 A1cf APOBEC1 complementation factor gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20160616 MGI PMID:24812305 733349 A1cf APOBEC1 complementation factor gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20170810 MGI PMID:17190866 733349 A1cf APOBEC1 complementation factor gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20171026 MGI PMID:27548259 733349 A1cf APOBEC1 complementation factor gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20220915 MGI PMID:35907876 733349 A1cf APOBEC1 complementation factor gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20170810 MGI PMID:26356605 733349 A1cf APOBEC1 complementation factor gene MP:0005630 increased lung weight IAGP N RGD:5509061 20160616 MGI PMID:17450150 733349 A1cf APOBEC1 complementation factor gene MP:0005630 increased lung weight IAGP N RGD:5509061 20180920 MGI PMID:26891723 733349 A1cf APOBEC1 complementation factor gene MP:0005630 increased lung weight IAGP N RGD:5509061 20200206 MGI PMID:31209364 733349 A1cf APOBEC1 complementation factor gene MP:0005630 increased lung weight IAGP N RGD:5509061 20220915 MGI PMID:35907876 733349 A1cf APOBEC1 complementation factor gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220811 MGI 733349 A1cf APOBEC1 complementation factor gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0005665 increased circulating noradrenaline level IAGP N RGD:5509061 20160616 MGI PMID:19328205 733349 A1cf APOBEC1 complementation factor gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20170810 MGI PMID:26356605 733349 A1cf APOBEC1 complementation factor gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20171116 MGI PMID:27184846 733349 A1cf APOBEC1 complementation factor gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20200206 MGI PMID:31209364 733349 A1cf APOBEC1 complementation factor gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20240620 MGI PMID:35680100 733349 A1cf APOBEC1 complementation factor gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20181018 MGI PMID:24658400 733349 A1cf APOBEC1 complementation factor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20160616 MGI PMID:16260633 733349 A1cf APOBEC1 complementation factor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20160616 MGI PMID:22869620 733349 A1cf APOBEC1 complementation factor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20171026 MGI PMID:27548259 733349 A1cf APOBEC1 complementation factor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20180503 MGI PMID:29438013 733349 A1cf APOBEC1 complementation factor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20200206 MGI PMID:31209364 733349 A1cf APOBEC1 complementation factor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20220811 MGI PMID:35358843 733349 A1cf APOBEC1 complementation factor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20220915 MGI PMID:35907876 733349 A1cf APOBEC1 complementation factor gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20230914 MGI PMID:37233188 733349 A1cf APOBEC1 complementation factor gene MP:0006141 abnormal atrioventricular node conduction IAGP N RGD:5509061 20160616 MGI PMID:18794341 733349 A1cf APOBEC1 complementation factor gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20160616 MGI PMID:21220308 733349 A1cf APOBEC1 complementation factor gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20160616 MGI PMID:19328205 733349 A1cf APOBEC1 complementation factor gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20160616 MGI PMID:15662031 733349 A1cf APOBEC1 complementation factor gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20160616 MGI PMID:16260633 733349 A1cf APOBEC1 complementation factor gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20170810 MGI PMID:17190866 733349 A1cf APOBEC1 complementation factor gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20170831 MGI PMID:19850880 733349 A1cf APOBEC1 complementation factor gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20230914 MGI PMID:37233188 733349 A1cf APOBEC1 complementation factor gene MP:0006321 increased myocardial fiber number IAGP N RGD:5509061 20160929 MGI PMID:25787764 733349 A1cf APOBEC1 complementation factor gene MP:0006321 increased myocardial fiber number IAGP N RGD:5509061 20180222 MGI PMID:28783163 733349 A1cf APOBEC1 complementation factor gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20160616 MGI PMID:16260633 733349 A1cf APOBEC1 complementation factor gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20160616 MGI PMID:21521762 733349 A1cf APOBEC1 complementation factor gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20171026 MGI PMID:27548259 733349 A1cf APOBEC1 complementation factor gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20200206 MGI PMID:31209364 733349 A1cf APOBEC1 complementation factor gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20210603 MGI PMID:33571905 733349 A1cf APOBEC1 complementation factor gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20230914 MGI PMID:37233188 733349 A1cf APOBEC1 complementation factor gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20240314 MGI PMID:36108935 733349 A1cf APOBEC1 complementation factor gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20240314 MGI PMID:36108935 733349 A1cf APOBEC1 complementation factor gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20170810 MGI PMID:17190866 733349 A1cf APOBEC1 complementation factor gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20170810 MGI PMID:17190866 733349 A1cf APOBEC1 complementation factor gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20160616 MGI PMID:19376970 733349 A1cf APOBEC1 complementation factor gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210429 MGI PMID:27956576 733349 A1cf APOBEC1 complementation factor gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 733349 A1cf APOBEC1 complementation factor gene MP:0010334 pleural effusion IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0010334 pleural effusion IAGP N RGD:5509061 20170810 MGI PMID:17190866 733349 A1cf APOBEC1 complementation factor gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20160616 MGI PMID:17823658 733349 A1cf APOBEC1 complementation factor gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20160616 MGI PMID:22992950 733349 A1cf APOBEC1 complementation factor gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20220811 MGI PMID:35358843 733349 A1cf APOBEC1 complementation factor gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0010505 abnormal T wave IAGP N RGD:5509061 20160616 MGI PMID:22869620 733349 A1cf APOBEC1 complementation factor gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20160616 MGI PMID:17823658 733349 A1cf APOBEC1 complementation factor gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20160616 MGI PMID:21220308 733349 A1cf APOBEC1 complementation factor gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20160616 MGI PMID:22869620 733349 A1cf APOBEC1 complementation factor gene MP:0010563 increased heart right ventricle size IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20160616 MGI PMID:16260633 733349 A1cf APOBEC1 complementation factor gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20160616 MGI PMID:19597047 733349 A1cf APOBEC1 complementation factor gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20160616 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20160616 MGI PMID:22375032 733349 A1cf APOBEC1 complementation factor gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20220915 MGI PMID:35907876 733349 A1cf APOBEC1 complementation factor gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20181018 MGI PMID:24658400 733349 A1cf APOBEC1 complementation factor gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20180920 MGI PMID:26891723 733349 A1cf APOBEC1 complementation factor gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20220915 MGI PMID:35907876 733349 A1cf APOBEC1 complementation factor gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20240314 MGI PMID:36108935 733349 A1cf APOBEC1 complementation factor gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20160616 MGI PMID:22869620 733349 A1cf APOBEC1 complementation factor gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20160616 MGI PMID:19328205 733349 A1cf APOBEC1 complementation factor gene MP:0010768 mortality/aging IAGP N RGD:5509061 20210429 MGI PMID:27956576 733349 A1cf APOBEC1 complementation factor gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20170810 MGI PMID:26356605 733349 A1cf APOBEC1 complementation factor gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20181018 MGI PMID:24658400 733349 A1cf APOBEC1 complementation factor gene MP:0010959 abnormal oxidative phosphorylation IAGP N RGD:5509061 20170810 MGI PMID:26356605 733349 A1cf APOBEC1 complementation factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20171116 MGI PMID:27184846 733349 A1cf APOBEC1 complementation factor gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16055734 733349 A1cf APOBEC1 complementation factor gene MP:0011424 decreased urine uric acid level IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20220811 MGI PMID:35358843 733349 A1cf APOBEC1 complementation factor gene MP:0011633 abnormal mitochondrial shape IAGP N RGD:5509061 20170810 MGI PMID:26356605 733349 A1cf APOBEC1 complementation factor gene MP:0011634 abnormal mitochondrial inner membrane morphology IAGP N RGD:5509061 20170810 MGI PMID:26356605 733349 A1cf APOBEC1 complementation factor gene MP:0011915 increased heart left atrium weight IAGP N RGD:5509061 20160616 MGI PMID:24812305 733349 A1cf APOBEC1 complementation factor gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20160616 MGI PMID:24200690 733349 A1cf APOBEC1 complementation factor gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20170810 MGI PMID:17190866 733349 A1cf APOBEC1 complementation factor gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20171026 MGI PMID:27548259 733349 A1cf APOBEC1 complementation factor gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20200206 MGI PMID:31209364 733349 A1cf APOBEC1 complementation factor gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20210603 MGI PMID:33571905 733349 A1cf APOBEC1 complementation factor gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20230914 MGI PMID:37233188 733349 A1cf APOBEC1 complementation factor gene MP:0011953 prolonged PQ interval IAGP N RGD:5509061 20160616 MGI PMID:21220308 733349 A1cf APOBEC1 complementation factor gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20160616 MGI PMID:19376970 733349 A1cf APOBEC1 complementation factor gene MP:0012688 abnormal heart ventricles weight IAGP N RGD:5509061 20160616 MGI PMID:24812305 733349 A1cf APOBEC1 complementation factor gene MP:0012688 abnormal heart ventricles weight IAGP N RGD:5509061 20200206 MGI PMID:31209364 733349 A1cf APOBEC1 complementation factor gene MP:0013272 abnormal translation IAGP N RGD:5509061 20161208 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20160616 MGI PMID:23948483 733349 A1cf APOBEC1 complementation factor gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20170810 MGI PMID:26356605 733349 A1cf APOBEC1 complementation factor gene MP:0014239 abnormal intracellular organelle morphology IAGP N RGD:5509061 20240620 MGI PMID:35680100 733349 A1cf APOBEC1 complementation factor gene MP:0020367 increased heart iron level IAGP N RGD:5509061 20161020 MGI PMID:22375032 733349 A1cf APOBEC1 complementation factor gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:24812305 733349 A1cf APOBEC1 complementation factor gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20230914 MGI PMID:37233188 733349 A1cf APOBEC1 complementation factor gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:17823658 733349 A1cf APOBEC1 complementation factor gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:20644257 733349 A1cf APOBEC1 complementation factor gene MP:0021160 decreased heart right ventricle wall thickness IAGP N RGD:5509061 20230914 MGI PMID:37233188 733349 A1cf APOBEC1 complementation factor gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:17916779 733349 A1cf APOBEC1 complementation factor gene MP:0030973 impaired gluconeogenesis IAGP N RGD:5509061 20200130 MGI PMID:31597092 733349 A1cf APOBEC1 complementation factor gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:19850880 733349 A1cf APOBEC1 complementation factor gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:22829020 733349 A1cf APOBEC1 complementation factor gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20230914 MGI PMID:37233188 733349 A1cf APOBEC1 complementation factor gene MP:0031216 decreased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20240620 MGI PMID:35680100 733349 A1cf APOBEC1 complementation factor gene MP:0031217 increased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20240418 MGI PMID:34831084 733349 A1cf APOBEC1 complementation factor gene MP:0031217 increased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20240620 MGI PMID:35680100 733349 A1cf APOBEC1 complementation factor gene MP:0031417 decreased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:23948483 733349 A1cf APOBEC1 complementation factor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15662031 733349 A1cf APOBEC1 complementation factor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:16260633 733349 A1cf APOBEC1 complementation factor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:17190866 733349 A1cf APOBEC1 complementation factor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:19376970 733349 A1cf APOBEC1 complementation factor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:21245375 733349 A1cf APOBEC1 complementation factor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:24658400 733349 A1cf APOBEC1 complementation factor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:31209364 733349 A1cf APOBEC1 complementation factor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:33571905 733349 A1cf APOBEC1 complementation factor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:35358843 733349 A1cf APOBEC1 complementation factor gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:37233188 733352 Ntsr2 neurotensin receptor 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20399236 733352 Ntsr2 neurotensin receptor 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:20399236 733352 Ntsr2 neurotensin receptor 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:14725975 733352 Ntsr2 neurotensin receptor 2 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:20399236 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:2364541 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:2364541 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:2364541 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:14758363 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:14758363 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:2364541 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:14758363 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:2364541 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:2364541 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:2364541 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:14575238 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:2364541 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0001406 abnormal gait IEA N RGD:5509061 20111116 MGI 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:2364541 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:2364541 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:2364541 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:14575238 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:21040848 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0002200 abnormal brain ventricular system morphology IAGP N RGD:5509061 20141003 MGI PMID:2364541 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21040848 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:14758363 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:21040848 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21040848 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:14575238 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:14758363 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0009688 abnormal spinal cord central canal morphology IAGP N RGD:5509061 20141003 MGI PMID:9600211 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0010151 abnormal spinal cord ependymal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11706940 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0010152 abnormal brain ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:11706940 733354 Napa N-ethylmaleimide sensitive fusion protein attachment protein alpha gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14758363 733355 Fgf4 fibroblast growth factor 4 gene MP:0000592 short tail IAGP N RGD:5509061 20170511 MGI PMID:26666435 733355 Fgf4 fibroblast growth factor 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170511 MGI PMID:26666435 733355 Fgf4 fibroblast growth factor 4 gene MP:0001394 circling IAGP N RGD:5509061 20170511 MGI PMID:26666435 733355 Fgf4 fibroblast growth factor 4 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20170511 MGI PMID:26666435 733355 Fgf4 fibroblast growth factor 4 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20161216 MGI PMID:7809630 733355 Fgf4 fibroblast growth factor 4 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20161216 MGI PMID:7809630 733355 Fgf4 fibroblast growth factor 4 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20161216 MGI PMID:7809630 733355 Fgf4 fibroblast growth factor 4 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10662638 733355 Fgf4 fibroblast growth factor 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10662638 733355 Fgf4 fibroblast growth factor 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10802662 733355 Fgf4 fibroblast growth factor 4 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20161216 MGI PMID:7809630 733355 Fgf4 fibroblast growth factor 4 gene MP:0005191 head tilt IAGP N RGD:5509061 20170511 MGI PMID:26666435 733355 Fgf4 fibroblast growth factor 4 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20161216 MGI PMID:7809630 733355 Fgf4 fibroblast growth factor 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210826 MGI 733355 Fgf4 fibroblast growth factor 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10802662 733355 Fgf4 fibroblast growth factor 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20161216 MGI PMID:7809630 733355 Fgf4 fibroblast growth factor 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733355 Fgf4 fibroblast growth factor 4 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20161216 MGI PMID:7809630 733355 Fgf4 fibroblast growth factor 4 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20170511 MGI PMID:26666435 733355 Fgf4 fibroblast growth factor 4 gene MP:0012182 abnormal presomitic mesoderm morphology IAGP N RGD:5509061 20170511 MGI PMID:26666435 733355 Fgf4 fibroblast growth factor 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:10391239 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9690472 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:19479951 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:9690472 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9690472 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:10391239 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:10391239 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19479951 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:19479951 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12001066 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10391239 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12001066 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:19479951 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:19479951 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0008149 abnormal costovertebral joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9690472 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19479951 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:10391239 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:10391239 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19479951 733358 Rfng RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10391239 733360 Chrnd cholinergic receptor, nicotinic, delta polypeptide gene MP:0001297 microphthalmia IEA N RGD:5509061 20220519 MGI 733360 Chrnd cholinergic receptor, nicotinic, delta polypeptide gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 733360 Chrnd cholinergic receptor, nicotinic, delta polypeptide gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20220519 MGI 733360 Chrnd cholinergic receptor, nicotinic, delta polypeptide gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 733360 Chrnd cholinergic receptor, nicotinic, delta polypeptide gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 733360 Chrnd cholinergic receptor, nicotinic, delta polypeptide gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 733360 Chrnd cholinergic receptor, nicotinic, delta polypeptide gene MP:0002989 small kidney IEA N RGD:5509061 20220519 MGI 733360 Chrnd cholinergic receptor, nicotinic, delta polypeptide gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20220519 MGI 733360 Chrnd cholinergic receptor, nicotinic, delta polypeptide gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 733368 Cd79b CD79B antigen gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:12097390 733368 Cd79b CD79B antigen gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:21841126 733368 Cd79b CD79B antigen gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:15024049 733368 Cd79b CD79B antigen gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:16818674 733368 Cd79b CD79B antigen gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11136817 733368 Cd79b CD79B antigen gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11514602 733368 Cd79b CD79B antigen gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12165571 733368 Cd79b CD79B antigen gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19727123 733368 Cd79b CD79B antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:19727123 733368 Cd79b CD79B antigen gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:19727123 733368 Cd79b CD79B antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16818674 733368 Cd79b CD79B antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19727123 733368 Cd79b CD79B antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21841126 733368 Cd79b CD79B antigen gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 733368 Cd79b CD79B antigen gene MP:0002403 abnormal pre-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12165571 733368 Cd79b CD79B antigen gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15024049 733368 Cd79b CD79B antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16818674 733368 Cd79b CD79B antigen gene MP:0002496 increased IgD level IAGP N RGD:5509061 20141003 MGI PMID:16818674 733368 Cd79b CD79B antigen gene MP:0002619 abnormal lymphocyte morphology IEA N RGD:5509061 20190418 MGI 733368 Cd79b CD79B antigen gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:19727123 733368 Cd79b CD79B antigen gene MP:0004978 decreased B-1 B cell number IEA N RGD:5509061 20190103 MGI 733368 Cd79b CD79B antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15024049 733368 Cd79b CD79B antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21841126 733368 Cd79b CD79B antigen gene MP:0005022 abnormal immature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12165571 733368 Cd79b CD79B antigen gene MP:0005022 abnormal immature B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15024049 733368 Cd79b CD79B antigen gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15024049 733368 Cd79b CD79B antigen gene MP:0005432 abnormal pro-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12165571 733368 Cd79b CD79B antigen gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20190103 MGI 733368 Cd79b CD79B antigen gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:19727123 733368 Cd79b CD79B antigen gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 733368 Cd79b CD79B antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 733368 Cd79b CD79B antigen gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:15024049 733368 Cd79b CD79B antigen gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:16818674 733368 Cd79b CD79B antigen gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:15024049 733368 Cd79b CD79B antigen gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11136817 733368 Cd79b CD79B antigen gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15024049 733368 Cd79b CD79B antigen gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21841126 733368 Cd79b CD79B antigen gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:11136817 733368 Cd79b CD79B antigen gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:11136817 733368 Cd79b CD79B antigen gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:21841126 733368 Cd79b CD79B antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11136817 733368 Cd79b CD79B antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:11514602 733368 Cd79b CD79B antigen gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15024049 733368 Cd79b CD79B antigen gene MP:0008212 absent mature B cells IAGP N RGD:5509061 20141003 MGI PMID:11514602 733368 Cd79b CD79B antigen gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15024049 733368 Cd79b CD79B antigen gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:11136817 733368 Cd79b CD79B antigen gene MP:0008233 abnormal pro-B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12165571 733368 Cd79b CD79B antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16818674 733368 Cd79b CD79B antigen gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20190103 MGI 733369 Basp1 brain abundant, membrane attached signal protein 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10871284 733369 Basp1 brain abundant, membrane attached signal protein 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:10871284 733369 Basp1 brain abundant, membrane attached signal protein 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:10871284 733369 Basp1 brain abundant, membrane attached signal protein 1 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10871284 733369 Basp1 brain abundant, membrane attached signal protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10871284 733369 Basp1 brain abundant, membrane attached signal protein 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10871284 733369 Basp1 brain abundant, membrane attached signal protein 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10871284 733369 Basp1 brain abundant, membrane attached signal protein 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:10871284 733369 Basp1 brain abundant, membrane attached signal protein 1 gene MP:0004243 abnormal motor nerve collateral sprouting IAGP N RGD:5509061 20141003 MGI PMID:10871284 733369 Basp1 brain abundant, membrane attached signal protein 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:10871284 733369 Basp1 brain abundant, membrane attached signal protein 1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:10871284 733369 Basp1 brain abundant, membrane attached signal protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10871284 733369 Basp1 brain abundant, membrane attached signal protein 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:10871284 733371 Sdcbp syndecan binding protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20210610 MGI PMID:33602969 733371 Sdcbp syndecan binding protein gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20160519 MGI PMID:25880340 733373 Hip1r huntingtin interacting protein 1 related gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20210722 MGI PMID:15121852 733373 Hip1r huntingtin interacting protein 1 related gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210722 MGI PMID:15121852 733373 Hip1r huntingtin interacting protein 1 related gene MP:0001265 decreased body size IAGP N RGD:5509061 20210722 MGI PMID:15121852 733373 Hip1r huntingtin interacting protein 1 related gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20161201 MGI 733373 Hip1r huntingtin interacting protein 1 related gene MP:0001505 hunched posture IAGP N RGD:5509061 20210610 MGI PMID:15121852 733373 Hip1r huntingtin interacting protein 1 related gene MP:0002083 premature death IAGP N RGD:5509061 20210722 MGI PMID:15121852 733373 Hip1r huntingtin interacting protein 1 related gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15121852 733373 Hip1r huntingtin interacting protein 1 related gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:15121852 733373 Hip1r huntingtin interacting protein 1 related gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20210722 MGI PMID:15121852 733373 Hip1r huntingtin interacting protein 1 related gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 733373 Hip1r huntingtin interacting protein 1 related gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:15121852 733373 Hip1r huntingtin interacting protein 1 related gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210722 MGI PMID:30224518 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20180531 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:14638864 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0000507 absent digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0000603 pale liver IEA N RGD:5509061 20221103 MGI 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0000623 decreased salivation IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16651618 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22952456 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:16983341 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:14638864 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:16983341 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16983341 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:16983341 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:14638864 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:14638864 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:14638864 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:16983341 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:14638864 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:16983341 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001665 chronic diarrhea IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20221103 MGI 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:22952456 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:22952456 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001722 pale yolk sac IEA N RGD:5509061 20221103 MGI 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:14638864 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20221103 MGI 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22952456 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:14638864 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:14638864 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:16651618 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:22952456 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:22952456 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:22952456 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0003717 pallor IEA N RGD:5509061 20221103 MGI 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0003756 abnormal hard palate morphology IAGP N RGD:5509061 20141003 MGI PMID:16651618 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:16983341 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20221103 MGI 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20221103 MGI 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0004848 abnormal liver size IEA N RGD:5509061 20221103 MGI 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0005310 abnormal salivary gland physiology IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0005650 abnormal limb bud morphology IEA N RGD:5509061 20221103 MGI 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0008879 submandibular gland inflammation IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:16983341 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0009595 enlarged corneocyte envelope IAGP N RGD:5509061 20141003 MGI PMID:14638864 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0009596 abnormal stratum corneum lipid matrix formation IAGP N RGD:5509061 20141003 MGI PMID:14638864 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0009597 impaired stratum corneum desquamation IAGP N RGD:5509061 20141003 MGI PMID:14638864 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19717635 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16983341 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210422 MGI 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22952456 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20221103 MGI 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0020220 decreased tear production IAGP N RGD:5509061 20150514 MGI PMID:24551030 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0030570 abnormal piliary canal morphology IAGP N RGD:5509061 20180524 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0030605 abnormal corneocyte morphology IAGP N RGD:5509061 20180628 MGI PMID:12032844 733375 St14 suppression of tumorigenicity 14 (colon carcinoma) gene MP:0030605 abnormal corneocyte morphology IAGP N RGD:5509061 20180628 MGI PMID:16983341 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0001304 cataract IEA N RGD:5509061 20160804 MGI 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0001320 small pupil IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0001851 eye inflammation IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0003313 abnormal locomotor activation IEA N RGD:5509061 20160804 MGI 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0004062 dilated heart right atrium IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0004094 abnormal M line morphology IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20180531 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0010553 prolonged HV interval IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20220811 MGI 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20161124 MGI PMID:26616005 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0011953 prolonged PQ interval IAGP N RGD:5509061 20170907 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0030567 abnormal I band morphology IAGP N RGD:5509061 20180531 MGI PMID:22945801 733379 Cap2 cyclase associated actin cytoskeleton regulatory protein 2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:26616005 733382 Kcnn3 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 3 gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:10988076 733382 Kcnn3 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 3 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:22554781 733382 Kcnn3 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 3 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:10988076 733382 Kcnn3 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 3 gene MP:0012010 parturition failure IAGP N RGD:5509061 20141003 MGI PMID:10988076 733382 Kcnn3 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 3 gene MP:0020844 abnormal pulmonary respiratory rate response IAGP N RGD:5509061 20181101 MGI PMID:10988076 733387 Zwint ZW10 interactor gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 733387 Zwint ZW10 interactor gene MP:0002718 abnormal inner cell mass morphology IEA N RGD:5509061 20241017 MGI 733387 Zwint ZW10 interactor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733387 Zwint ZW10 interactor gene MP:0011189 small embryonic epiblast IEA N RGD:5509061 20241017 MGI 733387 Zwint ZW10 interactor gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 733387 Zwint ZW10 interactor gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240801 MGI 733390 Cep19 centrosomal protein 19 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20201022 MGI 733390 Cep19 centrosomal protein 19 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:24268657 733390 Cep19 centrosomal protein 19 gene MP:0001258 decreased body length IEA N RGD:5509061 20201022 MGI 733390 Cep19 centrosomal protein 19 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:24268657 733390 Cep19 centrosomal protein 19 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:24268657 733390 Cep19 centrosomal protein 19 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:24268657 733390 Cep19 centrosomal protein 19 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:24268657 733390 Cep19 centrosomal protein 19 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200402 MGI 733390 Cep19 centrosomal protein 19 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:24268657 733390 Cep19 centrosomal protein 19 gene MP:0001925 male infertility IEA N RGD:5509061 20240523 MGI 733390 Cep19 centrosomal protein 19 gene MP:0001926 female infertility IEA N RGD:5509061 20240523 MGI 733390 Cep19 centrosomal protein 19 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210128 MGI 733390 Cep19 centrosomal protein 19 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 733390 Cep19 centrosomal protein 19 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20190502 MGI 733390 Cep19 centrosomal protein 19 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:24268657 733390 Cep19 centrosomal protein 19 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:24268657 733390 Cep19 centrosomal protein 19 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:24268657 733390 Cep19 centrosomal protein 19 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:24268657 733390 Cep19 centrosomal protein 19 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:24268657 733390 Cep19 centrosomal protein 19 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 733390 Cep19 centrosomal protein 19 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:24268657 733390 Cep19 centrosomal protein 19 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20190502 MGI 733390 Cep19 centrosomal protein 19 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:24268657 733390 Cep19 centrosomal protein 19 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17849011 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20191003 MGI PMID:27959908 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19419305 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:7344126 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12817751 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:8055108 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:9359030 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000149 abnormal scapula morphology IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000161 scoliosis IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000162 lordosis IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:15625282 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8055108 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000192 abnormal mineral level IAGP N RGD:5509061 20141003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:9359030 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20191003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000706 small thymus IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:19419305 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9359030 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19419305 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:7344126 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:8055108 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:16680148 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:9359030 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001562 abnormal circulating calcium level IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001565 abnormal circulating phosphate level IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7344126 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20191003 MGI PMID:27959908 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001925 male infertility IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0001926 female infertility IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20111116 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7344126 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:7344126 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:8055108 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:7344126 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:9359030 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:19419305 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:7344126 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:8055108 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0002933 joint inflammation IEA N RGD:5509061 20111116 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:12817751 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003189 fused joints IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003195 calcinosis IAGP N RGD:5509061 20141003 MGI PMID:7344126 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003195 calcinosis IAGP N RGD:5509061 20181122 MGI PMID:28592560 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003195 calcinosis IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003196 calcified skin IAGP N RGD:5509061 20141003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003196 calcified skin IAGP N RGD:5509061 20181122 MGI PMID:28592560 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003196 calcified skin IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003198 calcified tendon IAGP N RGD:5509061 20141003 MGI PMID:19419305 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003200 calcified joint IAGP N RGD:5509061 20141003 MGI PMID:19419305 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003200 calcified joint IAGP N RGD:5509061 20141003 MGI PMID:7344126 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003200 calcified joint IAGP N RGD:5509061 20141003 MGI PMID:8055108 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003200 calcified joint IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003330 abnormal auditory tube morphology IAGP N RGD:5509061 20191003 MGI PMID:27959908 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:7344126 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:8055108 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0003653 decreased skin turgor IEA N RGD:5509061 20111116 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:19419305 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:7344126 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:8055108 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:9359030 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004181 abnormal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004357 long tibia IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004480 abnormal round window morphology IAGP N RGD:5509061 20191003 MGI PMID:27959908 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004612 fusion of vertebral bodies IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004665 abnormal stapedial artery morphology IAGP N RGD:5509061 20191003 MGI PMID:27959908 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004685 calcified intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:12817751 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004685 calcified intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:7344126 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20191003 MGI PMID:27959908 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:12817751 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0005190 osteomyelitis IEA N RGD:5509061 20111116 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0005504 abnormal ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:8055108 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0005504 abnormal ligament morphology IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15625282 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0006018 abnormal tympanic membrane morphology IAGP N RGD:5509061 20191003 MGI PMID:27959908 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0006133 calcified artery IAGP N RGD:5509061 20141003 MGI PMID:19419305 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0006133 calcified artery IAGP N RGD:5509061 20141003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0006188 calcified retina IAGP N RGD:5509061 20141003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0006325 impaired hearing IEA N RGD:5509061 20111116 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0006357 abnormal circulating mineral level IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0006392 abnormal nucleus pulposus morphology IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0008915 fused carpal bones IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0009393 abnormal resting posture IEA N RGD:5509061 20111116 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0009877 exostosis IAGP N RGD:5509061 20141003 MGI PMID:19419305 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0010099 abnormal thoracic cage shape IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:19419305 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0010522 calcified aorta IAGP N RGD:5509061 20141003 MGI PMID:15625282 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0010522 calcified aorta IAGP N RGD:5509061 20141003 MGI PMID:19419305 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0010522 calcified aorta IAGP N RGD:5509061 20141003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0010522 calcified aorta IAGP N RGD:5509061 20190228 MGI PMID:25479107 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0010522 calcified aorta IAGP N RGD:5509061 20201112 MGI PMID:7344126 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0010678 abnormal skin adnexa morphology IAGP N RGD:5509061 20141003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0010935 increased airway resistance IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0011315 abnormal kidney arcuate artery morphology IAGP N RGD:5509061 20191003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0011317 abnormal renal artery morphology IAGP N RGD:5509061 20191003 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20141003 MGI PMID:9359030 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20191003 MGI PMID:27959908 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0013941 abnormal enthesis morphology IAGP N RGD:5509061 20160310 MGI PMID:9359030 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0013945 abnormal elbow joint morphology IEA N RGD:5509061 20181018 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0014099 abnormal chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:7344126 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:12817751 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20240523 MGI 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0020903 increased middle ear goblet cell number IAGP N RGD:5509061 20191219 MGI PMID:27959908 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030110 incudomalleolar fusion IAGP N RGD:5509061 20191219 MGI PMID:27959908 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030226 middle ear polyps IAGP N RGD:5509061 20191003 MGI PMID:27959908 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030410 middle ear effusion IAGP N RGD:5509061 20191003 MGI PMID:27959908 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030413 tympanic membrane retraction IAGP N RGD:5509061 20191003 MGI PMID:27959908 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030422 abnormal outer ear cartilage morphology IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030533 abnormal snout skin morphology IAGP N RGD:5509061 20181122 MGI PMID:28592560 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030776 calcified calcaneal tendon IAGP N RGD:5509061 20181004 MGI PMID:12817751 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030776 calcified calcaneal tendon IAGP N RGD:5509061 20181004 MGI PMID:19419305 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030776 calcified calcaneal tendon IAGP N RGD:5509061 20181004 MGI PMID:7344126 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030783 abnormal posterior longitudinal ligament morphology IAGP N RGD:5509061 20181004 MGI PMID:9359030 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030783 abnormal posterior longitudinal ligament morphology IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030807 abnormal forelimb joint morphology IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030811 abnormal hand joint morphology IAGP N RGD:5509061 20200416 MGI PMID:24770645 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030837 abnormal knee joint morphology IAGP N RGD:5509061 20181025 MGI PMID:19419305 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030863 decreased joint mobility IAGP N RGD:5509061 20181101 MGI PMID:19419305 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030863 decreased joint mobility IAGP N RGD:5509061 20181101 MGI PMID:23798568 733393 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1 gene MP:0030863 decreased joint mobility IAGP N RGD:5509061 20190228 MGI PMID:25479107 733394 Tas1r3 taste receptor, type 1, member 3 gene MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19244541 733394 Tas1r3 taste receptor, type 1, member 3 gene MP:0004209 abnormal sweet taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12869700 733394 Tas1r3 taste receptor, type 1, member 3 gene MP:0004209 abnormal sweet taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:14636554 733394 Tas1r3 taste receptor, type 1, member 3 gene MP:0004213 abnormal umami taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12869700 733394 Tas1r3 taste receptor, type 1, member 3 gene MP:0004213 abnormal umami taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:14636554 733394 Tas1r3 taste receptor, type 1, member 3 gene MP:0005423 abnormal somatic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12869700 733394 Tas1r3 taste receptor, type 1, member 3 gene MP:0005423 abnormal somatic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:14636554 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17167098 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19420255 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17167098 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:19420255 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20150827 MGI PMID:19420255 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20150827 MGI PMID:19420255 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17167098 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19420255 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:19420255 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:19420255 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19420255 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17167098 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17167098 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17167098 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:17167098 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17167098 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:19420255 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:19420255 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:19420255 733397 Apba2 amyloid beta precursor protein binding family A member 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17167098 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20170928 MGI PMID:14623956 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:14623956 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16207763 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14623956 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:16207763 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:14623956 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20230727 MGI PMID:29467333 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:16611695 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0003095 abnormal cornea stroma development IAGP N RGD:5509061 20141003 MGI PMID:16207763 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20040494 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0004054 abnormal periocular mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:16207763 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0004054 abnormal periocular mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:16611695 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:16611695 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:20040494 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0005195 abnormal posterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:16611695 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0006162 thick eyelids IAGP N RGD:5509061 20141225 MGI PMID:16611695 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0008881 absent Harderian gland IAGP N RGD:5509061 20141003 MGI PMID:14623956 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0008881 absent Harderian gland IAGP N RGD:5509061 20141003 MGI PMID:16207763 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0008970 choanal atresia IAGP N RGD:5509061 20141003 MGI PMID:14623956 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0008972 ethmoturbinate hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14623956 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20160324 MGI PMID:16207763 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0009742 increased cornea stroma thickness IAGP N RGD:5509061 20141225 MGI PMID:16611695 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0010706 ventral rotation of lens IAGP N RGD:5509061 20160324 MGI PMID:14623956 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0010706 ventral rotation of lens IAGP N RGD:5509061 20160324 MGI PMID:16207763 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0010707 decreased ventral retina size IAGP N RGD:5509061 20160324 MGI PMID:14623956 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0010707 decreased ventral retina size IAGP N RGD:5509061 20160324 MGI PMID:16207763 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0010708 absent iris stroma IAGP N RGD:5509061 20160324 MGI PMID:16207763 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0010710 absent sclera IAGP N RGD:5509061 20160324 MGI PMID:16207763 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:14623956 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:16207763 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:16611695 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0010712 absent nasolacrimal duct IAGP N RGD:5509061 20141211 MGI PMID:14623956 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14623956 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16207763 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17207476 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0011964 increased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:16611695 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0013744 abnormal conjunctival sac morphology IAGP N RGD:5509061 20160324 MGI PMID:16207763 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0030093 absent maxillary sinus IAGP N RGD:5509061 20170928 MGI PMID:14623956 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0030181 persistent nasal fins IAGP N RGD:5509061 20171012 MGI PMID:14623956 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0030326 decreased periocular mesenchyme apoptosis IAGP N RGD:5509061 20171109 MGI PMID:16207763 733398 Aldh1a3 aldehyde dehydrogenase family 1, subfamily A3 gene MP:0030326 decreased periocular mesenchyme apoptosis IAGP N RGD:5509061 20171109 MGI PMID:16611695 733401 Src Rous sarcoma oncogene gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:7958873 733401 Src Rous sarcoma oncogene gene MP:0000119 abnormal tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0000119 abnormal tooth eruption IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0000125 absent incisors IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21628573 733401 Src Rous sarcoma oncogene gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0000435 shortened head IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20160804 MGI 733401 Src Rous sarcoma oncogene gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7958873 733401 Src Rous sarcoma oncogene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7958873 733401 Src Rous sarcoma oncogene gene MP:0001265 decreased body size IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:7958873 733401 Src Rous sarcoma oncogene gene MP:0001405 impaired coordination IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:7958873 733401 Src Rous sarcoma oncogene gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16107610 733401 Src Rous sarcoma oncogene gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:7958873 733401 Src Rous sarcoma oncogene gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7958873 733401 Src Rous sarcoma oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21628573 733401 Src Rous sarcoma oncogene gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:16107610 733401 Src Rous sarcoma oncogene gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 733401 Src Rous sarcoma oncogene gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21628573 733401 Src Rous sarcoma oncogene gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0006400 decreased molar number IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21628573 733401 Src Rous sarcoma oncogene gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7958873 733401 Src Rous sarcoma oncogene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7958873 733401 Src Rous sarcoma oncogene gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8634424 733401 Src Rous sarcoma oncogene gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20141003 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0020396 abnormal social recognition IAGP N RGD:5509061 20171109 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0030069 broad face IAGP N RGD:5509061 20171019 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0030132 periodontium inflammation IAGP N RGD:5509061 20171005 MGI PMID:1997203 733401 Src Rous sarcoma oncogene gene MP:0030420 short basicranium IAGP N RGD:5509061 20171214 MGI PMID:26464974 733401 Src Rous sarcoma oncogene gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:26464974 733404 Prss12 serine protease 12 neurotrypsin (motopsin) gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 733404 Prss12 serine protease 12 neurotrypsin (motopsin) gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 733404 Prss12 serine protease 12 neurotrypsin (motopsin) gene MP:0001262 decreased body weight IEA N RGD:5509061 20211021 MGI 733404 Prss12 serine protease 12 neurotrypsin (motopsin) gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:20092579 733404 Prss12 serine protease 12 neurotrypsin (motopsin) gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20111116 MGI 733404 Prss12 serine protease 12 neurotrypsin (motopsin) gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 733404 Prss12 serine protease 12 neurotrypsin (motopsin) gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20111116 MGI 733404 Prss12 serine protease 12 neurotrypsin (motopsin) gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:20092579 733404 Prss12 serine protease 12 neurotrypsin (motopsin) gene MP:0011971 increased circulating lactate dehydrogenase level IEA N RGD:5509061 20210128 MGI 733404 Prss12 serine protease 12 neurotrypsin (motopsin) gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20211014 MGI PMID:20092579 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0000160 kyphosis IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20170309 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001258 decreased body length IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21249153 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170309 MGI PMID:25485098 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170309 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21249153 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22751104 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21249153 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20170309 MGI PMID:25485098 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170309 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20170309 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20170309 MGI PMID:25485098 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20170309 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:21249153 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:22751104 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:21249153 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20170309 MGI PMID:25485098 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20170309 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:22751104 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0004144 hypotonia IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:22751104 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:22751104 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20170309 MGI PMID:25485098 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20170309 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:22751104 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20170309 MGI PMID:25485098 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20170309 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20170309 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0008918 microgliosis IAGP N RGD:5509061 20170309 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21249153 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20170309 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20170309 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0010062 decreased creatine level IAGP N RGD:5509061 20141003 MGI PMID:21249153 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0010062 decreased creatine level IAGP N RGD:5509061 20141003 MGI PMID:22751104 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0010062 decreased creatine level IAGP N RGD:5509061 20170309 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0010062 decreased creatine level IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0010062 decreased creatine level IAGP N RGD:5509061 20180927 MGI PMID:25485098 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0010065 decreased circulating creatine level IAGP N RGD:5509061 20141003 MGI PMID:21249153 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0010065 decreased circulating creatine level IAGP N RGD:5509061 20170309 MGI PMID:25485098 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:21249153 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20170309 MGI PMID:25485098 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20180920 MGI PMID:30013483 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:21249153 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0020083 decreased hippocampus volume IAGP N RGD:5509061 20170309 MGI PMID:27466184 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0030632 increased urine creatine level IAGP N RGD:5509061 20180927 MGI PMID:22751104 733405 Slc6a8 solute carrier family 6 (neurotransmitter transporter, creatine), member 8 gene MP:0030633 decreased urine creatine level IAGP N RGD:5509061 20180927 MGI PMID:25485098 733409 Rxrg retinoid X receptor gamma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10336693 733409 Rxrg retinoid X receptor gamma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8799145 733409 Rxrg retinoid X receptor gamma gene MP:0002822 catalepsy IAGP N RGD:5509061 20141003 MGI PMID:10336693 733409 Rxrg retinoid X receptor gamma gene MP:0004037 increased muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:10336693 733409 Rxrg retinoid X receptor gamma gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:10336693 733410 Omd osteomodulin gene MP:0009456 impaired cued conditioning behavior IEA N RGD:5509061 20141003 MGI 733411 Aptx aprataxin gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 733411 Aptx aprataxin gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20181227 MGI 733411 Aptx aprataxin gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 733411 Aptx aprataxin gene MP:0001393 ataxia IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0001523 impaired righting response IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 733411 Aptx aprataxin gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:21390131 733411 Aptx aprataxin gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 733411 Aptx aprataxin gene MP:0010183 abnormal CD4-positive helper T cell morphology IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0010947 abnormal single-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:19103743 733411 Aptx aprataxin gene MP:0014127 increased thymoma incidence IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0014378 increased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0021001 impaired neuron physiology IAGP N RGD:5509061 20220106 MGI PMID:34723800 733411 Aptx aprataxin gene MP:0021009 abnormal synaptic physiology IAGP N RGD:5509061 20220106 MGI PMID:34723800 733416 Mef2d myocyte enhancer factor 2D gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18079970 733416 Mef2d myocyte enhancer factor 2D gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18079970 733416 Mef2d myocyte enhancer factor 2D gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:22496871 733416 Mef2d myocyte enhancer factor 2D gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20160623 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22496871 733416 Mef2d myocyte enhancer factor 2D gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22496871 733416 Mef2d myocyte enhancer factor 2D gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22496871 733416 Mef2d myocyte enhancer factor 2D gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22496871 733416 Mef2d myocyte enhancer factor 2D gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:22496871 733416 Mef2d myocyte enhancer factor 2D gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22496871 733416 Mef2d myocyte enhancer factor 2D gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20160623 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20160623 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18079970 733416 Mef2d myocyte enhancer factor 2D gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20141003 MGI PMID:18079970 733416 Mef2d myocyte enhancer factor 2D gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20160623 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20160623 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0006075 abnormal retina cone bipolar cell morphology IAGP N RGD:5509061 20160623 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0008275 failure of endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17336904 733416 Mef2d myocyte enhancer factor 2D gene MP:0008278 failure of sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:17336904 733416 Mef2d myocyte enhancer factor 2D gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20160623 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20170112 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20160623 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20160623 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20160623 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0008583 absent photoreceptor inner segment IAGP N RGD:5509061 20160623 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20160623 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:17786239 733416 Mef2d myocyte enhancer factor 2D gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17336904 733416 Mef2d myocyte enhancer factor 2D gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20160623 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20160623 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20160623 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0014333 short retina cone cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:25757744 733416 Mef2d myocyte enhancer factor 2D gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:25757744 733417 Atxn10 ataxin 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:16924013 733417 Atxn10 ataxin 10 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20150723 MGI PMID:16924013 733417 Atxn10 ataxin 10 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733417 Atxn10 ataxin 10 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 733417 Atxn10 ataxin 10 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 733419 Pcx pyruvate carboxylase gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0003839 abnormal insulin clearance IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210520 MGI 733419 Pcx pyruvate carboxylase gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 733419 Pcx pyruvate carboxylase gene MP:0010052 increased grip strength IEA N RGD:5509061 20181227 MGI 733419 Pcx pyruvate carboxylase gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 733419 Pcx pyruvate carboxylase gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20211021 MGI 733419 Pcx pyruvate carboxylase gene MP:0010953 abnormal fatty acid oxidation IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733419 Pcx pyruvate carboxylase gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20230119 MGI PMID:36441025 733419 Pcx pyruvate carboxylase gene MP:0030973 impaired gluconeogenesis IAGP N RGD:5509061 20230119 MGI PMID:36441025 733420 Ppp1r3b protein phosphatase 1, regulatory subunit 3B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19275933 733420 Ppp1r3b protein phosphatase 1, regulatory subunit 3B gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19275933 733420 Ppp1r3b protein phosphatase 1, regulatory subunit 3B gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:19275933 733420 Ppp1r3b protein phosphatase 1, regulatory subunit 3B gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:19275933 733420 Ppp1r3b protein phosphatase 1, regulatory subunit 3B gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19275933 733420 Ppp1r3b protein phosphatase 1, regulatory subunit 3B gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19275933 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:15147966 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20200618 MGI PMID:15147966 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15130877 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:12072376 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:15988472 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15988472 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:11867747 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:15130877 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:18380672 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:11867747 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15926931 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15130877 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12072376 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:15926931 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0003194 abnormal frequency of paradoxical sleep IAGP N RGD:5509061 20141003 MGI PMID:18380672 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:11867747 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:11867747 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:11867747 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:12072376 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:15130877 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:11867747 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18719666 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0005471 decreased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:11867747 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:15988472 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:11867747 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:12072376 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15130877 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15926931 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11867747 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12072376 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:12072376 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18380672 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12072376 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15130877 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:15988472 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0010167 decreased response to stress-induced hyperthermia IAGP N RGD:5509061 20141003 MGI PMID:15988472 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:11867747 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0010962 decreased compact bone mass IAGP N RGD:5509061 20200618 MGI PMID:15147966 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15130877 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:12072376 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:11867747 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0031074 increased circulating type I collagen C-terminal telopeptide level IAGP N RGD:5509061 20200618 MGI PMID:15147966 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:11867747 733422 Mchr1 melanin-concentrating hormone receptor 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:15130877 733423 Rabac1 Rab acceptor 1 (prenylated) gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 733423 Rabac1 Rab acceptor 1 (prenylated) gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20181227 MGI 733425 Neo1 neogenin gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:12636918 733425 Neo1 neogenin gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16723533 733425 Neo1 neogenin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12636918 733427 Cfh complement component factor h gene MP:0000314 schistocytosis IAGP N RGD:5509061 20141003 MGI PMID:17517971 733427 Cfh complement component factor h gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:17921253 733427 Cfh complement component factor h gene MP:0001265 decreased body size IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17921253 733427 Cfh complement component factor h gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23799019 733427 Cfh complement component factor h gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0001394 circling IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0001577 anemia IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17517971 733427 Cfh complement component factor h gene MP:0002083 premature death IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:18202746 733427 Cfh complement component factor h gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0003099 retina detachment IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17517971 733427 Cfh complement component factor h gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:23799019 733427 Cfh complement component factor h gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:17517971 733427 Cfh complement component factor h gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17921253 733427 Cfh complement component factor h gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0005161 hematuria IAGP N RGD:5509061 20141003 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0005161 hematuria IAGP N RGD:5509061 20141003 MGI PMID:17517971 733427 Cfh complement component factor h gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17921253 733427 Cfh complement component factor h gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17921253 733427 Cfh complement component factor h gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:18202746 733427 Cfh complement component factor h gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 733427 Cfh complement component factor h gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17517971 733427 Cfh complement component factor h gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0005615 increased susceptibility to type III hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17921253 733427 Cfh complement component factor h gene MP:0006080 brain ischemia IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0006134 artery occlusion IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20141003 MGI PMID:17921253 733427 Cfh complement component factor h gene MP:0006242 white pupil IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:17921253 733427 Cfh complement component factor h gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0010061 increased creatine level IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0010215 abnormal circulating complement protein level IAGP N RGD:5509061 20141003 MGI PMID:17517971 733427 Cfh complement component factor h gene MP:0011310 abnormal kidney capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0011507 abnormal kidney thrombosis IAGP N RGD:5509061 20141003 MGI PMID:17517971 733427 Cfh complement component factor h gene MP:0011507 abnormal kidney thrombosis IAGP N RGD:5509061 20201210 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0011508 abnormal glomerular capillary thrombosis IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0011512 mesangial cell interposition IAGP N RGD:5509061 20141003 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0011566 abnormal complement protein level IAGP N RGD:5509061 20141003 MGI PMID:17517971 733427 Cfh complement component factor h gene MP:0011738 anasarca IAGP N RGD:5509061 20141003 MGI PMID:17517971 733427 Cfh complement component factor h gene MP:0012049 increased susceptilbility to retina ischemic injury IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20141003 MGI PMID:17921253 733427 Cfh complement component factor h gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20141003 MGI PMID:17921253 733427 Cfh complement component factor h gene MP:0012553 decreased serum complement activity IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0012609 decreased complement C5 level IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0020216 decreased circulating complement protein level IAGP N RGD:5509061 20141003 MGI PMID:17517971 733427 Cfh complement component factor h gene MP:0020216 decreased circulating complement protein level IAGP N RGD:5509061 20141003 MGI PMID:18202746 733427 Cfh complement component factor h gene MP:0020216 decreased circulating complement protein level IAGP N RGD:5509061 20190704 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0020216 decreased circulating complement protein level IAGP N RGD:5509061 20201001 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0020518 renal glomerular protein deposits IAGP N RGD:5509061 20180125 MGI PMID:18202746 733427 Cfh complement component factor h gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:12091909 733427 Cfh complement component factor h gene MP:0031159 abnormal hepatic portal vein thrombosis IAGP N RGD:5509061 20201210 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0031161 abnormal kidney venous thrombosis IAGP N RGD:5509061 20201210 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0031167 abnormal lung thrombosis IAGP N RGD:5509061 20201210 MGI PMID:28057640 733427 Cfh complement component factor h gene MP:0031168 abnormal brain thrombosis IAGP N RGD:5509061 20201210 MGI PMID:28057640 733429 Fbn2 fibrillin 2 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20201022 MGI 733429 Fbn2 fibrillin 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200514 MGI 733429 Fbn2 fibrillin 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200514 MGI 733429 Fbn2 fibrillin 2 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20201022 MGI 733429 Fbn2 fibrillin 2 gene MP:0000458 abnormal mandible morphology IEA N RGD:5509061 20201022 MGI 733429 Fbn2 fibrillin 2 gene MP:0000552 abnormal radius morphology IEA N RGD:5509061 20201022 MGI 733429 Fbn2 fibrillin 2 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20180830 MGI PMID:29208648 733429 Fbn2 fibrillin 2 gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20201022 MGI 733429 Fbn2 fibrillin 2 gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20201022 MGI 733429 Fbn2 fibrillin 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:10700192 733429 Fbn2 fibrillin 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:11285249 733429 Fbn2 fibrillin 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:11470817 733429 Fbn2 fibrillin 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:20161761 733429 Fbn2 fibrillin 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20180830 MGI PMID:29208648 733429 Fbn2 fibrillin 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:11470817 733429 Fbn2 fibrillin 2 gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20200514 MGI 733429 Fbn2 fibrillin 2 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20200514 MGI 733429 Fbn2 fibrillin 2 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:20161761 733429 Fbn2 fibrillin 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20200514 MGI 733429 Fbn2 fibrillin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20161761 733429 Fbn2 fibrillin 2 gene MP:0001314 cornea opacity IEA N RGD:5509061 20210826 MGI 733429 Fbn2 fibrillin 2 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 733429 Fbn2 fibrillin 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20200514 MGI 733429 Fbn2 fibrillin 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20161761 733429 Fbn2 fibrillin 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20161761 733429 Fbn2 fibrillin 2 gene MP:0001785 edema IAGP N RGD:5509061 20180830 MGI PMID:29208648 733429 Fbn2 fibrillin 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20180830 MGI PMID:29208648 733429 Fbn2 fibrillin 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20200514 MGI 733429 Fbn2 fibrillin 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:20161761 733429 Fbn2 fibrillin 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20180830 MGI PMID:29208648 733429 Fbn2 fibrillin 2 gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20180830 MGI PMID:29208648 733429 Fbn2 fibrillin 2 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20200514 MGI 733429 Fbn2 fibrillin 2 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20201231 MGI 733429 Fbn2 fibrillin 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:20729550 733429 Fbn2 fibrillin 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 733429 Fbn2 fibrillin 2 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20200514 MGI 733429 Fbn2 fibrillin 2 gene MP:0002187 abnormal fibula morphology IEA N RGD:5509061 20201022 MGI 733429 Fbn2 fibrillin 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20180830 MGI PMID:29208648 733429 Fbn2 fibrillin 2 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:11470817 733429 Fbn2 fibrillin 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 733429 Fbn2 fibrillin 2 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:20729550 733429 Fbn2 fibrillin 2 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 733429 Fbn2 fibrillin 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201022 MGI 733429 Fbn2 fibrillin 2 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:20729550 733429 Fbn2 fibrillin 2 gene MP:0004083 polysyndactyly IAGP N RGD:5509061 20141003 MGI PMID:11470817 733429 Fbn2 fibrillin 2 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20161761 733429 Fbn2 fibrillin 2 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20201022 MGI 733429 Fbn2 fibrillin 2 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20201022 MGI 733429 Fbn2 fibrillin 2 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20201231 MGI 733429 Fbn2 fibrillin 2 gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:20161761 733429 Fbn2 fibrillin 2 gene MP:0004857 abnormal heart weight IEA N RGD:5509061 20211021 MGI 733429 Fbn2 fibrillin 2 gene MP:0005108 abnormal ulna morphology IEA N RGD:5509061 20201022 MGI 733429 Fbn2 fibrillin 2 gene MP:0005270 abnormal zygomatic bone morphology IEA N RGD:5509061 20201022 MGI 733429 Fbn2 fibrillin 2 gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20201022 MGI 733429 Fbn2 fibrillin 2 gene MP:0005298 abnormal clavicle morphology IEA N RGD:5509061 20201022 MGI 733429 Fbn2 fibrillin 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20180830 MGI PMID:29208648 733429 Fbn2 fibrillin 2 gene MP:0005542 cornea vascularization IEA N RGD:5509061 20210826 MGI 733429 Fbn2 fibrillin 2 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20210826 MGI 733429 Fbn2 fibrillin 2 gene MP:0008730 fused phalanges IAGP N RGD:5509061 20141003 MGI PMID:20161761 733429 Fbn2 fibrillin 2 gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20210128 MGI 733429 Fbn2 fibrillin 2 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:20161761 733429 Fbn2 fibrillin 2 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:20161761 733429 Fbn2 fibrillin 2 gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:16407178 733429 Fbn2 fibrillin 2 gene MP:0009874 abnormal interdigital cell death IAGP N RGD:5509061 20141003 MGI PMID:11470817 733429 Fbn2 fibrillin 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20161761 733429 Fbn2 fibrillin 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 733429 Fbn2 fibrillin 2 gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20211021 MGI 733429 Fbn2 fibrillin 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20529844 733429 Fbn2 fibrillin 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16407178 733429 Fbn2 fibrillin 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20529844 733429 Fbn2 fibrillin 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16407178 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0000286 abnormal mitral valve morphology IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:23131567 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20141003 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:23131567 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23131567 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23131567 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23131567 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23131567 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23131567 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0002747 abnormal aortic valve morphology IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0002928 abnormal bile duct morphology IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0002947 increased hemangioma incidence IEA N RGD:5509061 20210930 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:23131567 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0003619 abnormal urine color IAGP N RGD:5509061 20141003 MGI PMID:23131567 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0006064 abnormal superior vena cava morphology IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0008044 increased NK cell number IEA N RGD:5509061 20181227 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0008346 increased gamma-delta T cell number IEA N RGD:5509061 20201022 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:23131567 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0010490 abnormal inferior vena cava valve morphology IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:23131567 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23131567 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23131567 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23131567 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0013875 increased trigeminal neuroma incidence IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0013966 abnormal infrahyoid muscle morphology IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0013985 abnormal umbilical vein topology IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0013986 abnormal vitelline vein topology IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0014018 embryo tumor IEA N RGD:5509061 20171228 MGI 733431 Xpnpep1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble gene MP:0014023 abnormal intestine placement IEA N RGD:5509061 20171228 MGI 733436 Col5a1 collagen, type V, alpha 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16492673 733436 Col5a1 collagen, type V, alpha 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:16492673 733436 Col5a1 collagen, type V, alpha 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16492673 733436 Col5a1 collagen, type V, alpha 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20220721 MGI PMID:34740257 733436 Col5a1 collagen, type V, alpha 1 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20220721 MGI PMID:34740257 733436 Col5a1 collagen, type V, alpha 1 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20150924 MGI PMID:22159420 733436 Col5a1 collagen, type V, alpha 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15383546 733436 Col5a1 collagen, type V, alpha 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:15383546 733436 Col5a1 collagen, type V, alpha 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:16492673 733436 Col5a1 collagen, type V, alpha 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151112 MGI PMID:22159420 733436 Col5a1 collagen, type V, alpha 1 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:16492673 733436 Col5a1 collagen, type V, alpha 1 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20220721 MGI PMID:34740257 733436 Col5a1 collagen, type V, alpha 1 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20150924 MGI PMID:22159420 733436 Col5a1 collagen, type V, alpha 1 gene MP:0003093 abnormal cornea anterior stroma morphology IAGP N RGD:5509061 20150924 MGI PMID:22159420 733436 Col5a1 collagen, type V, alpha 1 gene MP:0003094 abnormal cornea posterior stroma morphology IAGP N RGD:5509061 20150924 MGI PMID:22159420 733436 Col5a1 collagen, type V, alpha 1 gene MP:0003096 increased corneal light-scattering IAGP N RGD:5509061 20150924 MGI PMID:22159420 733436 Col5a1 collagen, type V, alpha 1 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20150924 MGI PMID:22159420 733436 Col5a1 collagen, type V, alpha 1 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:15383546 733436 Col5a1 collagen, type V, alpha 1 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20220721 MGI PMID:16492673 733436 Col5a1 collagen, type V, alpha 1 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20220721 MGI PMID:34740257 733436 Col5a1 collagen, type V, alpha 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15383546 733436 Col5a1 collagen, type V, alpha 1 gene MP:0011650 abnormal cornea stroma collagen fibril morphology IAGP N RGD:5509061 20150924 MGI PMID:22159420 733437 Il1rn interleukin 1 receptor antagonist gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:15086551 733437 Il1rn interleukin 1 receptor antagonist gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:15086551 733437 Il1rn interleukin 1 receptor antagonist gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15086551 733437 Il1rn interleukin 1 receptor antagonist gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:15086551 733437 Il1rn interleukin 1 receptor antagonist gene MP:0001230 epidermal desquamation IAGP N RGD:5509061 20141003 MGI PMID:15086551 733437 Il1rn interleukin 1 receptor antagonist gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15086551 733437 Il1rn interleukin 1 receptor antagonist gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:15086551 733437 Il1rn interleukin 1 receptor antagonist gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12874179 733437 Il1rn interleukin 1 receptor antagonist gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15914123 733437 Il1rn interleukin 1 receptor antagonist gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8855299 733437 Il1rn interleukin 1 receptor antagonist gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9565638 733437 Il1rn interleukin 1 receptor antagonist gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9565638 733437 Il1rn interleukin 1 receptor antagonist gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:10749768 733437 Il1rn interleukin 1 receptor antagonist gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10637274 733437 Il1rn interleukin 1 receptor antagonist gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15914123 733437 Il1rn interleukin 1 receptor antagonist gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8855299 733437 Il1rn interleukin 1 receptor antagonist gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15749858 733437 Il1rn interleukin 1 receptor antagonist gene MP:0002433 abnormal T-helper 1 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15749858 733437 Il1rn interleukin 1 receptor antagonist gene MP:0002434 abnormal T-helper 2 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15749858 733437 Il1rn interleukin 1 receptor antagonist gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:10637274 733437 Il1rn interleukin 1 receptor antagonist gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:15749858 733437 Il1rn interleukin 1 receptor antagonist gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:15749858 733437 Il1rn interleukin 1 receptor antagonist gene MP:0003279 aneurysm IAGP N RGD:5509061 20201015 MGI PMID:10637274 733437 Il1rn interleukin 1 receptor antagonist gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:15086551 733437 Il1rn interleukin 1 receptor antagonist gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:12721360 733437 Il1rn interleukin 1 receptor antagonist gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15086551 733437 Il1rn interleukin 1 receptor antagonist gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20141003 MGI PMID:15086551 733437 Il1rn interleukin 1 receptor antagonist gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20141003 MGI PMID:19144317 733437 Il1rn interleukin 1 receptor antagonist gene MP:0003711 pathological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:15086551 733437 Il1rn interleukin 1 receptor antagonist gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20112392 733437 Il1rn interleukin 1 receptor antagonist gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15914123 733437 Il1rn interleukin 1 receptor antagonist gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:12874179 733437 Il1rn interleukin 1 receptor antagonist gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:15086551 733437 Il1rn interleukin 1 receptor antagonist gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:10749768 733437 Il1rn interleukin 1 receptor antagonist gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:15004178 733437 Il1rn interleukin 1 receptor antagonist gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11983917 733437 Il1rn interleukin 1 receptor antagonist gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15914123 733437 Il1rn interleukin 1 receptor antagonist gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20112392 733437 Il1rn interleukin 1 receptor antagonist gene MP:0006135 artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:10637274 733437 Il1rn interleukin 1 receptor antagonist gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15749858 733437 Il1rn interleukin 1 receptor antagonist gene MP:0008125 abnormal dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:15749858 733437 Il1rn interleukin 1 receptor antagonist gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20240613 MGI PMID:25725107 733437 Il1rn interleukin 1 receptor antagonist gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20112392 733437 Il1rn interleukin 1 receptor antagonist gene MP:0008592 decreased circulating interleukin-1 level IAGP N RGD:5509061 20141003 MGI PMID:8855299 733437 Il1rn interleukin 1 receptor antagonist gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:10749768 733437 Il1rn interleukin 1 receptor antagonist gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20112392 733437 Il1rn interleukin 1 receptor antagonist gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:19144317 733437 Il1rn interleukin 1 receptor antagonist gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:20112392 733437 Il1rn interleukin 1 receptor antagonist gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20112392 733437 Il1rn interleukin 1 receptor antagonist gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20112392 733437 Il1rn interleukin 1 receptor antagonist gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:8855299 733437 Il1rn interleukin 1 receptor antagonist gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15914123 733437 Il1rn interleukin 1 receptor antagonist gene MP:0010139 aortitis IAGP N RGD:5509061 20141003 MGI PMID:10637274 733437 Il1rn interleukin 1 receptor antagonist gene MP:0010139 aortitis IAGP N RGD:5509061 20141003 MGI PMID:15086551 733437 Il1rn interleukin 1 receptor antagonist gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15914123 733437 Il1rn interleukin 1 receptor antagonist gene MP:0031234 increased circulating serum amyloid protein level IAGP N RGD:5509061 20210225 MGI PMID:10749768 733439 Cmklr1 chemerin chemokine-like receptor 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19841182 733439 Cmklr1 chemerin chemokine-like receptor 1 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:19841182 733439 Cmklr1 chemerin chemokine-like receptor 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:19841182 733439 Cmklr1 chemerin chemokine-like receptor 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19841182 733439 Cmklr1 chemerin chemokine-like receptor 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19841182 733439 Cmklr1 chemerin chemokine-like receptor 1 gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19841182 733439 Cmklr1 chemerin chemokine-like receptor 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:18391062 733439 Cmklr1 chemerin chemokine-like receptor 1 gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:19841182 733439 Cmklr1 chemerin chemokine-like receptor 1 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18391062 733439 Cmklr1 chemerin chemokine-like receptor 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:19841182 733439 Cmklr1 chemerin chemokine-like receptor 1 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:19841182 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11590436 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11590436 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9395487 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11590436 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20161208 MGI PMID:20644257 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20161208 MGI PMID:20644257 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20161208 MGI PMID:20644257 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:11590436 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20161208 MGI PMID:20644257 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20161208 MGI PMID:20644257 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11590436 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11590436 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:11590436 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20161208 MGI PMID:20644257 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20161208 MGI PMID:20644257 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11590436 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11590436 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11590436 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11590436 733442 Eif4ebp1 eukaryotic translation initiation factor 4E binding protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23426372 733443 Ccnd3 cyclin D3 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23079655 733443 Ccnd3 cyclin D3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12502747 733443 Ccnd3 cyclin D3 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:12502747 733443 Ccnd3 cyclin D3 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15315760 733443 Ccnd3 cyclin D3 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:15315760 733443 Ccnd3 cyclin D3 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:23079656 733443 Ccnd3 cyclin D3 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:12502747 733443 Ccnd3 cyclin D3 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:23079655 733443 Ccnd3 cyclin D3 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:23079656 733443 Ccnd3 cyclin D3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12502747 733443 Ccnd3 cyclin D3 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:12502747 733443 Ccnd3 cyclin D3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15315760 733443 Ccnd3 cyclin D3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14706337 733443 Ccnd3 cyclin D3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23079656 733443 Ccnd3 cyclin D3 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14706337 733443 Ccnd3 cyclin D3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14706337 733443 Ccnd3 cyclin D3 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15315760 733443 Ccnd3 cyclin D3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23079655 733443 Ccnd3 cyclin D3 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:15315760 733443 Ccnd3 cyclin D3 gene MP:0002296 aspiration IAGP N RGD:5509061 20141003 MGI PMID:12502747 733443 Ccnd3 cyclin D3 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:23079655 733443 Ccnd3 cyclin D3 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15315760 733443 Ccnd3 cyclin D3 gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12502747 733443 Ccnd3 cyclin D3 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:12502747 733443 Ccnd3 cyclin D3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15315760 733443 Ccnd3 cyclin D3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23079655 733443 Ccnd3 cyclin D3 gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12502747 733443 Ccnd3 cyclin D3 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15315760 733443 Ccnd3 cyclin D3 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:15315760 733443 Ccnd3 cyclin D3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14706337 733443 Ccnd3 cyclin D3 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:14706337 733443 Ccnd3 cyclin D3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14706337 733443 Ccnd3 cyclin D3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23079655 733443 Ccnd3 cyclin D3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23079656 733443 Ccnd3 cyclin D3 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23079656 733443 Ccnd3 cyclin D3 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14706337 733443 Ccnd3 cyclin D3 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23079656 733443 Ccnd3 cyclin D3 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14706337 733443 Ccnd3 cyclin D3 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15315760 733443 Ccnd3 cyclin D3 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:23079656 733443 Ccnd3 cyclin D3 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23079656 733443 Ccnd3 cyclin D3 gene MP:0010268 decreased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14706337 733443 Ccnd3 cyclin D3 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23079655 733443 Ccnd3 cyclin D3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12502747 733443 Ccnd3 cyclin D3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12502747 733443 Ccnd3 cyclin D3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15315760 733443 Ccnd3 cyclin D3 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:14706337 733444 Tpcn1 two pore channel 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 733444 Tpcn1 two pore channel 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:23063126 733444 Tpcn1 two pore channel 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 733444 Tpcn1 two pore channel 1 gene MP:0002959 increased urine microalbumin level IEA N RGD:5509061 20211021 MGI 733444 Tpcn1 two pore channel 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 733444 Tpcn1 two pore channel 1 gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20211021 MGI 733445 Rdh7 retinol dehydrogenase 7 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20191017 MGI PMID:30566883 733445 Rdh7 retinol dehydrogenase 7 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20191017 MGI PMID:30566883 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:14730302 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:14730302 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0000549 absent limbs IEA N RGD:5509061 20111116 MGI 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:14730302 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:14730302 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0000571 interdigital webbing IEA N RGD:5509061 20111116 MGI 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0000576 clubfoot IEA N RGD:5509061 20111116 MGI 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:11983858 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:14730302 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20111116 MGI 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:18509036 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001914 hemorrhage IEA N RGD:5509061 20111116 MGI 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11983858 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20111116 MGI 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0002989 small kidney IEA N RGD:5509061 20111116 MGI 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0003675 kidney cyst IEA N RGD:5509061 20111116 MGI 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0005242 cryptophthalmos IAGP N RGD:5509061 20141003 MGI PMID:14730302 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0006203 eye hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0008854 bleb IEA N RGD:5509061 20111116 MGI 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11983858 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14730302 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0011961 abnormal cornea thickness IAGP N RGD:5509061 20160310 MGI PMID:10974668 733446 Grip1 glutamate receptor interacting protein 1 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:10974668 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0000111 cleft palate IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0000445 short snout IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0000597 delayed hepatic development IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190808 MGI 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20231207 MGI 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20190808 MGI 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17376816 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0020401 argininuria IAGP N RGD:5509061 20221124 MGI PMID:32504080 733449 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene MP:0020403 lysinuria IAGP N RGD:5509061 20221124 MGI PMID:32504080 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20160421 MGI 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17085481 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17085481 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17085481 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20221215 MGI 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17085481 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17085481 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20201022 MGI 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17085481 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160421 MGI 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20160421 MGI 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17085481 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17085481 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17085481 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17085481 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:17085481 733452 Hnrnpd heterogeneous nuclear ribonucleoprotein D gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:17085481 733458 Apoa5 apolipoprotein A-V gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11588264 733458 Apoa5 apolipoprotein A-V gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15117734 733458 Apoa5 apolipoprotein A-V gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11588264 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20161110 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0001263 weight loss IAGP N RGD:5509061 20161110 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20161110 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0002083 premature death IAGP N RGD:5509061 20161110 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20161110 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20161110 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20161110 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20161110 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20161110 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20161110 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20161110 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20171012 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20161110 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20171019 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20161110 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0031078 increased circulating troponin T level IAGP N RGD:5509061 20200618 MGI PMID:26785494 733460 Yme1l1 YME1-like 1 (S. cerevisiae) gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:26785494 733461 Tmlhe trimethyllysine hydroxylase, epsilon gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231221 MGI PMID:34728372 733461 Tmlhe trimethyllysine hydroxylase, epsilon gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20231221 MGI PMID:34728372 733461 Tmlhe trimethyllysine hydroxylase, epsilon gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20231221 MGI PMID:34728372 733461 Tmlhe trimethyllysine hydroxylase, epsilon gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20240523 MGI 733461 Tmlhe trimethyllysine hydroxylase, epsilon gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20240523 MGI 733461 Tmlhe trimethyllysine hydroxylase, epsilon gene MP:0001406 abnormal gait IEA N RGD:5509061 20240523 MGI 733461 Tmlhe trimethyllysine hydroxylase, epsilon gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20231221 MGI PMID:34728372 733461 Tmlhe trimethyllysine hydroxylase, epsilon gene MP:0003978 decreased circulating carnitine level IAGP N RGD:5509061 20231221 MGI PMID:34728372 733461 Tmlhe trimethyllysine hydroxylase, epsilon gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20231221 MGI PMID:34728372 733461 Tmlhe trimethyllysine hydroxylase, epsilon gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20231221 MGI PMID:34728372 733461 Tmlhe trimethyllysine hydroxylase, epsilon gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20231221 MGI PMID:34728372 733461 Tmlhe trimethyllysine hydroxylase, epsilon gene MP:0005283 increased unsaturated fatty acids level IAGP N RGD:5509061 20231221 MGI PMID:34728372 733461 Tmlhe trimethyllysine hydroxylase, epsilon gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20231221 MGI PMID:34728372 733461 Tmlhe trimethyllysine hydroxylase, epsilon gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20231221 MGI PMID:34728372 733461 Tmlhe trimethyllysine hydroxylase, epsilon gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20231221 MGI PMID:34728372 733465 Mak male germ cell-associated kinase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11971961 733465 Mak male germ cell-associated kinase gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11971961 733468 Adarb2 adenosine deaminase, RNA-specific, B2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 733468 Adarb2 adenosine deaminase, RNA-specific, B2 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20181227 MGI 733468 Adarb2 adenosine deaminase, RNA-specific, B2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 733468 Adarb2 adenosine deaminase, RNA-specific, B2 gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 733468 Adarb2 adenosine deaminase, RNA-specific, B2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20181206 MGI PMID:29719497 733468 Adarb2 adenosine deaminase, RNA-specific, B2 gene MP:0001513 limb grasping IEA N RGD:5509061 20181227 MGI 733468 Adarb2 adenosine deaminase, RNA-specific, B2 gene MP:0002989 small kidney IEA N RGD:5509061 20181227 MGI 733468 Adarb2 adenosine deaminase, RNA-specific, B2 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20181206 MGI PMID:29719497 733470 Optn optineurin gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160804 MGI 733470 Optn optineurin gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 733470 Optn optineurin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20231012 MGI PMID:33723228 733470 Optn optineurin gene MP:0002090 abnormal vision IAGP N RGD:5509061 20220602 MGI PMID:35436991 733470 Optn optineurin gene MP:0002090 abnormal vision IAGP N RGD:5509061 20231012 MGI PMID:33723228 733470 Optn optineurin gene MP:0004129 abnormal respiratory quotient IEA N RGD:5509061 20160804 MGI 733470 Optn optineurin gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20220602 MGI PMID:35436991 733470 Optn optineurin gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160804 MGI 733470 Optn optineurin gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20220602 MGI PMID:35436991 733470 Optn optineurin gene MP:0005391 vision/eye phenotype IAGP N RGD:5509061 20231019 MGI PMID:33723228 733470 Optn optineurin gene MP:0005405 axon degeneration IAGP N RGD:5509061 20220602 MGI PMID:35436991 733470 Optn optineurin gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20160804 MGI 733470 Optn optineurin gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20220602 MGI PMID:35436991 733470 Optn optineurin gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20220602 MGI PMID:35436991 733470 Optn optineurin gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20231012 MGI PMID:33723228 733470 Optn optineurin gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20220602 MGI PMID:35436991 733470 Optn optineurin gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20231012 MGI PMID:33723228 733470 Optn optineurin gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24244017 733470 Optn optineurin gene MP:0011275 abnormal behavioral response to light IAGP N RGD:5509061 20231012 MGI PMID:33723228 733470 Optn optineurin gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20220602 MGI PMID:35436991 733470 Optn optineurin gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20231012 MGI PMID:33723228 733470 Optn optineurin gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20231012 MGI PMID:33723228 733472 Slco3a1 solute carrier organic anion transporter family, member 3a1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20191017 MGI PMID:30063921 733472 Slco3a1 solute carrier organic anion transporter family, member 3a1 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20191017 MGI PMID:30063921 733472 Slco3a1 solute carrier organic anion transporter family, member 3a1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20191017 MGI PMID:30063921 733472 Slco3a1 solute carrier organic anion transporter family, member 3a1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20191017 MGI PMID:30063921 733472 Slco3a1 solute carrier organic anion transporter family, member 3a1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20191017 MGI PMID:30063921 733476 Mcpt4 mast cell protease 4 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12900518 733476 Mcpt4 mast cell protease 4 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:12900518 733477 Ccl17 C-C motif chemokine ligand 17 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:22539295 733477 Ccl17 C-C motif chemokine ligand 17 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:12615900 733477 Ccl17 C-C motif chemokine ligand 17 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 733477 Ccl17 C-C motif chemokine ligand 17 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:12615900 733477 Ccl17 C-C motif chemokine ligand 17 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22539295 733477 Ccl17 C-C motif chemokine ligand 17 gene MP:0008125 abnormal dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22539295 733477 Ccl17 C-C motif chemokine ligand 17 gene MP:0008556 abnormal tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22539295 733477 Ccl17 C-C motif chemokine ligand 17 gene MP:0008656 abnormal interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22539295 733479 Olfm1 olfactomedin 1 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220609 MGI PMID:17301160 733479 Olfm1 olfactomedin 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:17301160 733479 Olfm1 olfactomedin 1 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0009649 delayed embryo implantation IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0009945 abnormal accessory olfactory bulb morphology IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0030982 abnormal copulatory plug deposition IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0030983 failure of copulatory plug deposition IAGP N RGD:5509061 20220609 MGI PMID:26107991 733479 Olfm1 olfactomedin 1 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:26107991 733486 Hnrnpk heterogeneous nuclear ribonucleoprotein K gene MP:0001147 small testis IAGP N RGD:5509061 20220707 MGI PMID:35455958 733486 Hnrnpk heterogeneous nuclear ribonucleoprotein K gene MP:0001265 decreased body size IAGP N RGD:5509061 20220707 MGI PMID:35455958 733486 Hnrnpk heterogeneous nuclear ribonucleoprotein K gene MP:0001925 male infertility IAGP N RGD:5509061 20220707 MGI PMID:35455958 733486 Hnrnpk heterogeneous nuclear ribonucleoprotein K gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220707 MGI PMID:35455958 733486 Hnrnpk heterogeneous nuclear ribonucleoprotein K gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20220707 MGI PMID:35455958 733486 Hnrnpk heterogeneous nuclear ribonucleoprotein K gene MP:0009248 small caput epididymis IAGP N RGD:5509061 20220707 MGI PMID:35455958 733486 Hnrnpk heterogeneous nuclear ribonucleoprotein K gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220707 MGI PMID:35455958 733486 Hnrnpk heterogeneous nuclear ribonucleoprotein K gene MP:0031210 small cauda epididymis IAGP N RGD:5509061 20220707 MGI PMID:35455958 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:16275892 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:15833871 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:10843684 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19729478 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20160616 MGI PMID:24993099 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20160616 MGI PMID:24993099 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9558111 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10843684 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:12524535 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:16105698 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17138939 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:9558111 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0003326 liver failure IAGP N RGD:5509061 20141003 MGI PMID:15944310 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:16105698 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:16275892 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:16841089 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19729478 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10528159 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12618265 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:19729478 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17138939 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:15307189 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10843684 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17138939 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12524535 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20160616 MGI PMID:24993099 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17138939 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:10528159 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20160616 MGI PMID:24993099 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:12556387 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17138939 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:9558111 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:10843684 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15944310 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:18259609 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19603542 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008248 abnormal mononuclear phagocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17138939 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:19729478 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9558111 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:10843684 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9558111 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17138939 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:9558111 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:17138939 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:9558111 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:9558111 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:10843684 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:9558111 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20160616 MGI PMID:24993099 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19729478 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0008990 abnormal Ito cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19603542 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:16275892 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15944310 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20201022 MGI PMID:26740279 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0010759 decreased right ventricle systolic pressure IAGP N RGD:5509061 20160616 MGI PMID:24993099 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:16105698 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20201022 MGI PMID:26740279 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0020449 decreased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:19729478 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0020935 decreased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16841089 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:19079579 733487 Ccr5 C-C motif chemokine receptor 5 gene MP:0031054 bronchiolitis IAGP N RGD:5509061 20200709 MGI PMID:19079579 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:11592985 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:9794766 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:11592985 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11592985 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:11592985 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18519586 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:9794766 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20697430 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:20065093 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:9794766 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11592985 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15687262 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18519586 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11592985 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18519586 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:18519586 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0002349 abnormal afferent lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15687262 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0003201 extremity edema IEA N RGD:5509061 20111116 MGI 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0003390 lymphedema IAGP N RGD:5509061 20141003 MGI PMID:11592985 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0003390 lymphedema IAGP N RGD:5509061 20141003 MGI PMID:20179099 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20141003 MGI PMID:11592985 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0003659 abnormal lymph circulation IAGP N RGD:5509061 20141003 MGI PMID:18519586 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11592985 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9794766 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:9794766 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:9794766 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:9794766 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:9794766 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20065093 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0008778 abnormal lymphangiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20697430 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0010194 absent lymphatic vessels IAGP N RGD:5509061 20141003 MGI PMID:18519586 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0010194 absent lymphatic vessels IAGP N RGD:5509061 20141003 MGI PMID:20697430 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0010196 abnormal lymphatic vessel smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:20439428 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0010200 enlarged lymphatic vessel IAGP N RGD:5509061 20141003 MGI PMID:20439428 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18519586 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11592985 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18519586 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9794766 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20065093 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0012080 chylous ascites IAGP N RGD:5509061 20141003 MGI PMID:11592985 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0012080 chylous ascites IAGP N RGD:5509061 20141003 MGI PMID:18519586 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0012080 chylous ascites IAGP N RGD:5509061 20141003 MGI PMID:20179099 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0012732 abnormal perineural vascular plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:9794766 733489 Flt4 FMS-like tyrosine kinase 4 gene MP:0031440 lymphatic vessel hypoplasia IAGP N RGD:5509061 20220915 MGI PMID:20179099 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:12832489 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0001147 small testis IAGP N RGD:5509061 20200402 MGI PMID:30244837 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20200402 MGI PMID:30244837 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:12832489 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12832489 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18443292 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200402 MGI PMID:30244837 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0002006 neoplasm IAGP N RGD:5509061 20200402 MGI PMID:30244837 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12832489 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12832489 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12832489 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18443292 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:12832489 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200402 MGI PMID:30244837 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:12832489 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0008057 abnormal DNA replication IAGP N RGD:5509061 20200402 MGI PMID:30244837 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200402 MGI PMID:30244837 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18443292 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12832489 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12832489 733490 Bard1 BRCA1 associated RING domain 1 gene MP:0014040 increased cellular sensitivity to DNA damaging agents IAGP N RGD:5509061 20200402 MGI PMID:30244837 733492 Ltc4s leukotriene C4 synthase gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:22416124 733492 Ltc4s leukotriene C4 synthase gene MP:0002148 abnormal hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11319240 733492 Ltc4s leukotriene C4 synthase gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:14970333 733492 Ltc4s leukotriene C4 synthase gene MP:0002531 abnormal type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11319240 733492 Ltc4s leukotriene C4 synthase gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:11319240 733492 Ltc4s leukotriene C4 synthase gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:22416124 733492 Ltc4s leukotriene C4 synthase gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23624557 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0000018 small ears IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0000111 cleft palate IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0000433 microcephaly IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0000440 domed cranium IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0000445 short snout IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0000705 athymia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0001785 edema IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0002251 abnormal nasopharynx morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0002639 micrognathia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0003842 abnormal metopic suture morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0004205 absent hyoid bone IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0004385 interparietal bone hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0004420 parietal bone hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0004458 absent alisphenoid bone IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0004461 basisphenoid bone hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0004900 absent zygomatic arch IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0004911 absent mandibular condyloid process IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0004913 absent mandibular angle IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0009798 abnormal ophthalmic nerve morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0009799 abnormal maxillary nerve morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0009800 abnormal mandibular nerve morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0009899 hyoid bone hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0010652 absent aorticopulmonary septum IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0012090 midbrain hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0012176 abnormal head development IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0012178 absent frontonasal prominence IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0012264 hindbrain hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0012755 decreased cranial neural crest cell number IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0012761 increased cranial neural crest cell apoptosis IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0013267 first pharyngeal arch hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0014167 ectopic bone IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0020845 abnormal DNA-templated transcription IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0030250 frontonasal prominence hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0030343 maxillary prominence hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0030344 absent maxillary prominence IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0030347 mandibular prominence hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733494 Snrpb small nuclear ribonucleoprotein B gene MP:0030374 Meckel's cartilage hypoplasia IAGP N RGD:5509061 20230309 MGI PMID:35593225 733497 Plvap plasmalemma vesicle associated protein gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0003180 abnormal pulmonary endothelial cell surface IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0009699 hyperchylomicronemia IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22782339 733497 Plvap plasmalemma vesicle associated protein gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0011310 abnormal kidney capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:23237953 733497 Plvap plasmalemma vesicle associated protein gene MP:0011860 abnormal peritubular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23237953 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0002607 decreased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0003958 heart valve hyperplasia IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0010470 dilated ascending aorta IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0010620 thick mitral valve IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0010629 thick tricuspid valve IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0011929 abnormal aortic valve flow IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0011931 abnormal pulmonary valve flow IAGP N RGD:5509061 20190725 MGI PMID:25615642 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:17923703 733502 Galnt1 polypeptide N-acetylgalactosaminyltransferase 1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:25615642 733504 Mnat1 menage a trois 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:12376559 733504 Mnat1 menage a trois 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12376559 733504 Mnat1 menage a trois 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12376559 733504 Mnat1 menage a trois 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11387217 733504 Mnat1 menage a trois 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12376559 733504 Mnat1 menage a trois 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:12376559 733504 Mnat1 menage a trois 1 gene MP:0004074 abnormal Schwann cell precursor morphology IAGP N RGD:5509061 20141003 MGI PMID:12376559 733504 Mnat1 menage a trois 1 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:11387217 733504 Mnat1 menage a trois 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11387217 733508 Nr2f6 nuclear receptor subfamily 2, group F, member 6 gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20141003 MGI PMID:15741322 733508 Nr2f6 nuclear receptor subfamily 2, group F, member 6 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:15741322 733508 Nr2f6 nuclear receptor subfamily 2, group F, member 6 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20190502 MGI 733508 Nr2f6 nuclear receptor subfamily 2, group F, member 6 gene MP:0005447 abnormal synaptic norepinephrine release IAGP N RGD:5509061 20141003 MGI PMID:15741322 733508 Nr2f6 nuclear receptor subfamily 2, group F, member 6 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 733508 Nr2f6 nuclear receptor subfamily 2, group F, member 6 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:15741322 733508 Nr2f6 nuclear receptor subfamily 2, group F, member 6 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:15741322 733508 Nr2f6 nuclear receptor subfamily 2, group F, member 6 gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20171012 MGI PMID:15741322 733513 Brs3 bombesin-like receptor 3 gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18039774 733513 Brs3 bombesin-like receptor 3 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18039774 733513 Brs3 bombesin-like receptor 3 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:9367152 733513 Brs3 bombesin-like receptor 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18039774 733513 Brs3 bombesin-like receptor 3 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:9367152 733513 Brs3 bombesin-like receptor 3 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:9367152 733513 Brs3 bombesin-like receptor 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9367152 733513 Brs3 bombesin-like receptor 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18039774 733513 Brs3 bombesin-like receptor 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9367152 733513 Brs3 bombesin-like receptor 3 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9367152 733513 Brs3 bombesin-like receptor 3 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:9367152 733513 Brs3 bombesin-like receptor 3 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:9367152 733513 Brs3 bombesin-like receptor 3 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:18039774 733513 Brs3 bombesin-like receptor 3 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18719666 733513 Brs3 bombesin-like receptor 3 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18039774 733513 Brs3 bombesin-like receptor 3 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:9367152 733513 Brs3 bombesin-like receptor 3 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18039774 733513 Brs3 bombesin-like receptor 3 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:18039774 733513 Brs3 bombesin-like receptor 3 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:9367152 733513 Brs3 bombesin-like receptor 3 gene MP:0014441 decreased response to leptin IAGP N RGD:5509061 20240523 MGI PMID:9367152 733514 Rabep2 rabaptin, RAB GTPase binding effector protein 2 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20221229 MGI PMID:36167069 733516 Rgs14 regulator of G-protein signaling 14 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:20837545 733516 Rgs14 regulator of G-protein signaling 14 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:20837545 733516 Rgs14 regulator of G-protein signaling 14 gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:15525537 733516 Rgs14 regulator of G-protein signaling 14 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:20837545 733516 Rgs14 regulator of G-protein signaling 14 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:20837545 733516 Rgs14 regulator of G-protein signaling 14 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:20837545 733516 Rgs14 regulator of G-protein signaling 14 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:20837545 733516 Rgs14 regulator of G-protein signaling 14 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15525537 733516 Rgs14 regulator of G-protein signaling 14 gene MP:0014368 enhanced long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:20837545 733518 Smad9 SMAD family member 9 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16765933 733518 Smad9 SMAD family member 9 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:23610558 733518 Smad9 SMAD family member 9 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15899870 733518 Smad9 SMAD family member 9 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15899870 733518 Smad9 SMAD family member 9 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:23610558 733518 Smad9 SMAD family member 9 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16765933 733518 Smad9 SMAD family member 9 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:16765933 733518 Smad9 SMAD family member 9 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:19419974 733518 Smad9 SMAD family member 9 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19419974 733518 Smad9 SMAD family member 9 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16765933 733518 Smad9 SMAD family member 9 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16765933 733518 Smad9 SMAD family member 9 gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:16765933 733518 Smad9 SMAD family member 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15899870 733518 Smad9 SMAD family member 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16765933 733518 Smad9 SMAD family member 9 gene MP:0002208 abnormal germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16765933 733518 Smad9 SMAD family member 9 gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17967875 733518 Smad9 SMAD family member 9 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:16765933 733518 Smad9 SMAD family member 9 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:16765933 733518 Smad9 SMAD family member 9 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19419974 733518 Smad9 SMAD family member 9 gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:17967875 733518 Smad9 SMAD family member 9 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:16765933 733518 Smad9 SMAD family member 9 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17967875 733518 Smad9 SMAD family member 9 gene MP:0008069 abnormal joint mobility IAGP N RGD:5509061 20141003 MGI PMID:23610558 733518 Smad9 SMAD family member 9 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:17967875 733518 Smad9 SMAD family member 9 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:23610558 733518 Smad9 SMAD family member 9 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23610558 733518 Smad9 SMAD family member 9 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23610558 733518 Smad9 SMAD family member 9 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16765933 733518 Smad9 SMAD family member 9 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16765933 733518 Smad9 SMAD family member 9 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23610558 733519 Dhrs9 dehydrogenase/reductase 9 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20220217 MGI PMID:34953854 733520 Gpr85 G protein-coupled receptor 85 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18413613 733520 Gpr85 G protein-coupled receptor 85 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:18413613 733520 Gpr85 G protein-coupled receptor 85 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:18413613 733520 Gpr85 G protein-coupled receptor 85 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18413613 733522 Sdha succinate dehydrogenase complex, subunit A, flavoprotein (Fp) gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20210128 MGI 733522 Sdha succinate dehydrogenase complex, subunit A, flavoprotein (Fp) gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 733522 Sdha succinate dehydrogenase complex, subunit A, flavoprotein (Fp) gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20181227 MGI 733522 Sdha succinate dehydrogenase complex, subunit A, flavoprotein (Fp) gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20170105 MGI 733522 Sdha succinate dehydrogenase complex, subunit A, flavoprotein (Fp) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733522 Sdha succinate dehydrogenase complex, subunit A, flavoprotein (Fp) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 733522 Sdha succinate dehydrogenase complex, subunit A, flavoprotein (Fp) gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 733524 Ppp1r14a protein phosphatase 1, regulatory inhibitor subunit 14A gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20201231 MGI PMID:30948334 733524 Ppp1r14a protein phosphatase 1, regulatory inhibitor subunit 14A gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20201231 MGI PMID:30948334 733525 Gpnmb glycoprotein (transmembrane) nmb gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20141003 MGI PMID:10192392 733525 Gpnmb glycoprotein (transmembrane) nmb gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:16827931 733525 Gpnmb glycoprotein (transmembrane) nmb gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20150122 MGI PMID:24936834 733525 Gpnmb glycoprotein (transmembrane) nmb gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20150122 MGI PMID:24936834 733525 Gpnmb glycoprotein (transmembrane) nmb gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10192392 733525 Gpnmb glycoprotein (transmembrane) nmb gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16827931 733525 Gpnmb glycoprotein (transmembrane) nmb gene MP:0005199 abnormal iris pigment epithelium IAGP N RGD:5509061 20141003 MGI PMID:10192392 733525 Gpnmb glycoprotein (transmembrane) nmb gene MP:0005208 abnormal iris stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:10192392 733525 Gpnmb glycoprotein (transmembrane) nmb gene MP:0005257 abnormal intraocular pressure IAGP N RGD:5509061 20141003 MGI PMID:16827931 733525 Gpnmb glycoprotein (transmembrane) nmb gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210826 MGI 733525 Gpnmb glycoprotein (transmembrane) nmb gene MP:0006228 iris atrophy IAGP N RGD:5509061 20141003 MGI PMID:16827931 733525 Gpnmb glycoprotein (transmembrane) nmb gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10192392 733525 Gpnmb glycoprotein (transmembrane) nmb gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 733526 Rin1 Ras and Rab interactor 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12574403 733526 Rin1 Ras and Rab interactor 1 gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:12574403 733526 Rin1 Ras and Rab interactor 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12574403 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14517554 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0000472 abnormal stomach non-glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14517554 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14517554 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:14517554 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:14517554 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14517554 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14517554 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14517554 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:14517554 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:19520915 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0005211 increased stomach mucosa thickness IAGP N RGD:5509061 20141003 MGI PMID:14517554 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19520915 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16293230 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16293230 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0010809 abnormal club cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19520915 733529 Keap1 kelch-like ECH-associated protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14517554 733532 Nptn neuroplastin gene MP:0000745 tremors IEA N RGD:5509061 20160421 MGI 733532 Nptn neuroplastin gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20240523 MGI 733532 Nptn neuroplastin gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210128 MGI 733532 Nptn neuroplastin gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 733532 Nptn neuroplastin gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20201022 MGI 733532 Nptn neuroplastin gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 733532 Nptn neuroplastin gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 733532 Nptn neuroplastin gene MP:0001512 trunk curl IAGP N RGD:5509061 20171019 MGI PMID:26740663 733532 Nptn neuroplastin gene MP:0001513 limb grasping IEA N RGD:5509061 20201231 MGI 733532 Nptn neuroplastin gene MP:0001522 impaired swimming IAGP N RGD:5509061 20171019 MGI PMID:26740663 733532 Nptn neuroplastin gene MP:0001523 impaired righting response IAGP N RGD:5509061 20171019 MGI PMID:26740663 733532 Nptn neuroplastin gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210128 MGI 733532 Nptn neuroplastin gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20160421 MGI 733532 Nptn neuroplastin gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20160128 MGI PMID:24554721 733532 Nptn neuroplastin gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 733532 Nptn neuroplastin gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 733532 Nptn neuroplastin gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20171019 MGI PMID:26740663 733532 Nptn neuroplastin gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20171019 MGI PMID:26740663 733532 Nptn neuroplastin gene MP:0004562 abnormal inner hair cell synaptic ribbon morphology IAGP N RGD:5509061 20171019 MGI PMID:26740663 733532 Nptn neuroplastin gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 733532 Nptn neuroplastin gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20160128 MGI PMID:24554721 733532 Nptn neuroplastin gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201231 MGI 733532 Nptn neuroplastin gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20160128 MGI PMID:24554721 733532 Nptn neuroplastin gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 733532 Nptn neuroplastin gene MP:0005191 head tilt IAGP N RGD:5509061 20171019 MGI PMID:26740663 733532 Nptn neuroplastin gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 733532 Nptn neuroplastin gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 733532 Nptn neuroplastin gene MP:0006325 impaired hearing IAGP N RGD:5509061 20171019 MGI PMID:26740663 733532 Nptn neuroplastin gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 733532 Nptn neuroplastin gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20160421 MGI 733532 Nptn neuroplastin gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20160128 MGI PMID:24554721 733532 Nptn neuroplastin gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20160128 MGI PMID:24554721 733532 Nptn neuroplastin gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 733532 Nptn neuroplastin gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 733532 Nptn neuroplastin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20171019 MGI PMID:26740663 733532 Nptn neuroplastin gene MP:0014384 increased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:24554721 733532 Nptn neuroplastin gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 733533 Mcpt8 mast cell protease 8 gene MP:0002607 decreased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20664169 733533 Mcpt8 mast cell protease 8 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:20664169 733535 Pde9a phosphodiesterase 9A gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20151210 MGI PMID:25799991 733536 Ctsz cathepsin Z gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:20133781 733536 Ctsz cathepsin Z gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20133781 733536 Ctsz cathepsin Z gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230601 MGI 733536 Ctsz cathepsin Z gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20133781 733536 Ctsz cathepsin Z gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:20133781 733536 Ctsz cathepsin Z gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20133781 733536 Ctsz cathepsin Z gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20133781 733536 Ctsz cathepsin Z gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:20133781 733536 Ctsz cathepsin Z gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20133781 733538 Aplnr apelin receptor gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15087458 733538 Aplnr apelin receptor gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:19767528 733538 Aplnr apelin receptor gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20160623 MGI PMID:25062690 733538 Aplnr apelin receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19578099 733538 Aplnr apelin receptor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:19767528 733538 Aplnr apelin receptor gene MP:0001756 abnormal urination IAGP N RGD:5509061 20141003 MGI PMID:19578099 733538 Aplnr apelin receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19767528 733538 Aplnr apelin receptor gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 733538 Aplnr apelin receptor gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 733538 Aplnr apelin receptor gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20181227 MGI 733538 Aplnr apelin receptor gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20160623 MGI PMID:25062690 733538 Aplnr apelin receptor gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:19578099 733538 Aplnr apelin receptor gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20160623 MGI PMID:25062690 733538 Aplnr apelin receptor gene MP:0004012 increased pulmonary artery pressure IAGP N RGD:5509061 20160623 MGI PMID:25062690 733538 Aplnr apelin receptor gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:19767528 733538 Aplnr apelin receptor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19767528 733538 Aplnr apelin receptor gene MP:0006137 venoocclusion IAGP N RGD:5509061 20160623 MGI PMID:25062690 733538 Aplnr apelin receptor gene MP:0008779 abnormal maternal behavior IAGP N RGD:5509061 20141003 MGI PMID:19767528 733538 Aplnr apelin receptor gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 733538 Aplnr apelin receptor gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19767528 733538 Aplnr apelin receptor gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19578099 733538 Aplnr apelin receptor gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:19578099 733538 Aplnr apelin receptor gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:19767528 733541 Egr2 early growth response 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:8565822 733541 Egr2 early growth response 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:10704452 733541 Egr2 early growth response 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15695336 733541 Egr2 early growth response 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:18524893 733541 Egr2 early growth response 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19244508 733541 Egr2 early growth response 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:7935840 733541 Egr2 early growth response 2 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:19244508 733541 Egr2 early growth response 2 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:18524893 733541 Egr2 early growth response 2 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:19244508 733541 Egr2 early growth response 2 gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:20231872 733541 Egr2 early growth response 2 gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:22678062 733541 Egr2 early growth response 2 gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20170713 MGI PMID:27517863 733541 Egr2 early growth response 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:10704452 733541 Egr2 early growth response 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15695336 733541 Egr2 early growth response 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:16136673 733541 Egr2 early growth response 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:18524893 733541 Egr2 early growth response 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:19244508 733541 Egr2 early growth response 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:19805360 733541 Egr2 early growth response 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141030 MGI PMID:24493648 733541 Egr2 early growth response 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:12376559 733541 Egr2 early growth response 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:23792428 733541 Egr2 early growth response 2 gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12575949 733541 Egr2 early growth response 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19805360 733541 Egr2 early growth response 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:12575949 733541 Egr2 early growth response 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:19244508 733541 Egr2 early growth response 2 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:8224839 733541 Egr2 early growth response 2 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9102308 733541 Egr2 early growth response 2 gene MP:0001070 abnormal abducens nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9102308 733541 Egr2 early growth response 2 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9102308 733541 Egr2 early growth response 2 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:8224839 733541 Egr2 early growth response 2 gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18524893 733541 Egr2 early growth response 2 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18524893 733541 Egr2 early growth response 2 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8224839 733541 Egr2 early growth response 2 gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18524893 733541 Egr2 early growth response 2 gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18524893 733541 Egr2 early growth response 2 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15695336 733541 Egr2 early growth response 2 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16136673 733541 Egr2 early growth response 2 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19244508 733541 Egr2 early growth response 2 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7935840 733541 Egr2 early growth response 2 gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:10704452 733541 Egr2 early growth response 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12376559 733541 Egr2 early growth response 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19244508 733541 Egr2 early growth response 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15695336 733541 Egr2 early growth response 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18524893 733541 Egr2 early growth response 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8224839 733541 Egr2 early growth response 2 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15695336 733541 Egr2 early growth response 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10704452 733541 Egr2 early growth response 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12376559 733541 Egr2 early growth response 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19244508 733541 Egr2 early growth response 2 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:18524893 733541 Egr2 early growth response 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20160428 MGI PMID:25344368 733541 Egr2 early growth response 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:19244508 733541 Egr2 early growth response 2 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:20231872 733541 Egr2 early growth response 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10704452 733541 Egr2 early growth response 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:8565822 733541 Egr2 early growth response 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18344997 733541 Egr2 early growth response 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:20231872 733541 Egr2 early growth response 2 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:20231872 733541 Egr2 early growth response 2 gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20141003 MGI PMID:21900566 733541 Egr2 early growth response 2 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20160428 MGI PMID:25344368 733541 Egr2 early growth response 2 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10704452 733541 Egr2 early growth response 2 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15695336 733541 Egr2 early growth response 2 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19244508 733541 Egr2 early growth response 2 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7935840 733541 Egr2 early growth response 2 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141030 MGI PMID:24493648 733541 Egr2 early growth response 2 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20160428 MGI PMID:25344368 733541 Egr2 early growth response 2 gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:8565822 733541 Egr2 early growth response 2 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18524893 733541 Egr2 early growth response 2 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8224839 733541 Egr2 early growth response 2 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:8565822 733541 Egr2 early growth response 2 gene MP:0003029 alkalemia IAGP N RGD:5509061 20141003 MGI PMID:21900566 733541 Egr2 early growth response 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:8565822 733541 Egr2 early growth response 2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:8565822 733541 Egr2 early growth response 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:10704452 733541 Egr2 early growth response 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:8565822 733541 Egr2 early growth response 2 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8565822 733541 Egr2 early growth response 2 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:8565822 733541 Egr2 early growth response 2 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:10704452 733541 Egr2 early growth response 2 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141030 MGI PMID:24493648 733541 Egr2 early growth response 2 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20160428 MGI PMID:25344368 733541 Egr2 early growth response 2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:12376559 733541 Egr2 early growth response 2 gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:10704452 733541 Egr2 early growth response 2 gene MP:0003994 abnormal dorsal spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:10704452 733541 Egr2 early growth response 2 gene MP:0004074 abnormal Schwann cell precursor morphology IAGP N RGD:5509061 20141003 MGI PMID:12376559 733541 Egr2 early growth response 2 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:8565822 733541 Egr2 early growth response 2 gene MP:0004568 fusion of glossopharyngeal and vagus nerve IAGP N RGD:5509061 20141003 MGI PMID:19244508 733541 Egr2 early growth response 2 gene MP:0004568 fusion of glossopharyngeal and vagus nerve IAGP N RGD:5509061 20141003 MGI PMID:8224839 733541 Egr2 early growth response 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:8565822 733541 Egr2 early growth response 2 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:22678062 733541 Egr2 early growth response 2 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20231872 733541 Egr2 early growth response 2 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20170713 MGI PMID:27517863 733541 Egr2 early growth response 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19940179 733541 Egr2 early growth response 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10704452 733541 Egr2 early growth response 2 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141030 MGI PMID:24493648 733541 Egr2 early growth response 2 gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:18524893 733541 Egr2 early growth response 2 gene MP:0005576 decreased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:21900566 733541 Egr2 early growth response 2 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12575949 733541 Egr2 early growth response 2 gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20160428 MGI PMID:25344368 733541 Egr2 early growth response 2 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:15695336 733541 Egr2 early growth response 2 gene MP:0006276 abnormal autonomic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:21900566 733541 Egr2 early growth response 2 gene MP:0008150 decreased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:8565822 733541 Egr2 early growth response 2 gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:8565822 733541 Egr2 early growth response 2 gene MP:0008155 decreased diameter of radius IAGP N RGD:5509061 20141003 MGI PMID:8565822 733541 Egr2 early growth response 2 gene MP:0008156 decreased diameter of tibia IAGP N RGD:5509061 20141003 MGI PMID:8565822 733541 Egr2 early growth response 2 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:19244508 733541 Egr2 early growth response 2 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:19805360 733541 Egr2 early growth response 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22678062 733541 Egr2 early growth response 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20170713 MGI PMID:27517863 733541 Egr2 early growth response 2 gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20141003 MGI PMID:20231872 733541 Egr2 early growth response 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19940179 733541 Egr2 early growth response 2 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141030 MGI PMID:24493648 733541 Egr2 early growth response 2 gene MP:0010463 aorta stenosis IAGP N RGD:5509061 20160428 MGI PMID:25344368 733541 Egr2 early growth response 2 gene MP:0010591 enlarged aortic valve IAGP N RGD:5509061 20160428 MGI PMID:25344368 733541 Egr2 early growth response 2 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20160428 MGI PMID:25344368 733541 Egr2 early growth response 2 gene MP:0010595 abnormal aortic valve cusp morphology IAGP N RGD:5509061 20160428 MGI PMID:25344368 733541 Egr2 early growth response 2 gene MP:0010605 thick pulmonary valve cusps IAGP N RGD:5509061 20160428 MGI PMID:25344368 733541 Egr2 early growth response 2 gene MP:0011042 abnormal horizontal vestibuloocular reflex IAGP N RGD:5509061 20141003 MGI PMID:20231872 733541 Egr2 early growth response 2 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18524893 733541 Egr2 early growth response 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15695336 733541 Egr2 early growth response 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19244508 733541 Egr2 early growth response 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19940179 733541 Egr2 early growth response 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8224839 733541 Egr2 early growth response 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7903221 733541 Egr2 early growth response 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8224839 733541 Egr2 early growth response 2 gene MP:0011406 abnormal retrotrapezoid nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:21900566 733541 Egr2 early growth response 2 gene MP:0011730 increased myelin sheath thickness IAGP N RGD:5509061 20141030 MGI PMID:24493648 733541 Egr2 early growth response 2 gene MP:0011906 increased Schwann cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15695336 733541 Egr2 early growth response 2 gene MP:0011906 increased Schwann cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18524893 733541 Egr2 early growth response 2 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:22678062 733541 Egr2 early growth response 2 gene MP:0011994 increased nerve conduction velocity IAGP N RGD:5509061 20141030 MGI PMID:24493648 733541 Egr2 early growth response 2 gene MP:0012674 tomacula IAGP N RGD:5509061 20141030 MGI PMID:24493648 733541 Egr2 early growth response 2 gene MP:0012793 decreased rhombomere 3 size IAGP N RGD:5509061 20141003 MGI PMID:11857793 733541 Egr2 early growth response 2 gene MP:0012793 decreased rhombomere 3 size IAGP N RGD:5509061 20141003 MGI PMID:9102308 733541 Egr2 early growth response 2 gene MP:0012795 absent rhombomere 3 IAGP N RGD:5509061 20141003 MGI PMID:12575949 733541 Egr2 early growth response 2 gene MP:0012795 absent rhombomere 3 IAGP N RGD:5509061 20141003 MGI PMID:8224839 733541 Egr2 early growth response 2 gene MP:0012795 absent rhombomere 3 IAGP N RGD:5509061 20141003 MGI PMID:9102308 733541 Egr2 early growth response 2 gene MP:0012801 decreased rhombomere 5 size IAGP N RGD:5509061 20141003 MGI PMID:9102308 733541 Egr2 early growth response 2 gene MP:0012803 absent rhombomere 5 IAGP N RGD:5509061 20141003 MGI PMID:12575949 733541 Egr2 early growth response 2 gene MP:0012803 absent rhombomere 5 IAGP N RGD:5509061 20141003 MGI PMID:8224839 733541 Egr2 early growth response 2 gene MP:0012803 absent rhombomere 5 IAGP N RGD:5509061 20141003 MGI PMID:9102308 733541 Egr2 early growth response 2 gene MP:0012805 decreased rhombomere 6 size IAGP N RGD:5509061 20141003 MGI PMID:9102308 733541 Egr2 early growth response 2 gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:22678062 733542 Atp5pb ATP synthase peripheral stalk-membrane subunit b gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733546 Tamalin trafficking regulator and scaffold protein tamalin gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22396401 733546 Tamalin trafficking regulator and scaffold protein tamalin gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:17766434 733546 Tamalin trafficking regulator and scaffold protein tamalin gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:22396401 733546 Tamalin trafficking regulator and scaffold protein tamalin gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:17766434 733546 Tamalin trafficking regulator and scaffold protein tamalin gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20141003 MGI PMID:17766434 733546 Tamalin trafficking regulator and scaffold protein tamalin gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:22396401 733546 Tamalin trafficking regulator and scaffold protein tamalin gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:22396401 733551 Rem2 rad and gem related GTP binding protein 2 gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20180830 MGI PMID:29809135 733551 Rem2 rad and gem related GTP binding protein 2 gene MP:0001389 abnormal eye movement IAGP N RGD:5509061 20180830 MGI PMID:29809135 733551 Rem2 rad and gem related GTP binding protein 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20180830 MGI PMID:29809135 733551 Rem2 rad and gem related GTP binding protein 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20180830 MGI PMID:29809135 733551 Rem2 rad and gem related GTP binding protein 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20180830 MGI PMID:29809135 733551 Rem2 rad and gem related GTP binding protein 2 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20180830 MGI PMID:29809135 733551 Rem2 rad and gem related GTP binding protein 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20180830 MGI PMID:29809135 733551 Rem2 rad and gem related GTP binding protein 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20180830 MGI PMID:29809135 733551 Rem2 rad and gem related GTP binding protein 2 gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:29809135 733551 Rem2 rad and gem related GTP binding protein 2 gene MP:0020506 abnormal dendritic spine density IAGP N RGD:5509061 20180830 MGI PMID:29809135 733551 Rem2 rad and gem related GTP binding protein 2 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20180830 MGI PMID:29809135 733553 Pja2 praja ring finger ubiquitin ligase 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20240321 MGI PMID:38379085 733553 Pja2 praja ring finger ubiquitin ligase 2 gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20240321 MGI PMID:38379085 733553 Pja2 praja ring finger ubiquitin ligase 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20161201 MGI 733553 Pja2 praja ring finger ubiquitin ligase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240321 MGI PMID:38379085 733553 Pja2 praja ring finger ubiquitin ligase 2 gene MP:0001785 edema IAGP N RGD:5509061 20240321 MGI PMID:38379085 733553 Pja2 praja ring finger ubiquitin ligase 2 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20240321 MGI PMID:38379085 733553 Pja2 praja ring finger ubiquitin ligase 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20190502 MGI 733553 Pja2 praja ring finger ubiquitin ligase 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20240321 MGI PMID:38379085 733553 Pja2 praja ring finger ubiquitin ligase 2 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20240321 MGI PMID:38379085 733553 Pja2 praja ring finger ubiquitin ligase 2 gene MP:0011338 abnormal mesangial matrix morphology IAGP N RGD:5509061 20240321 MGI PMID:38379085 733553 Pja2 praja ring finger ubiquitin ligase 2 gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20240321 MGI PMID:38379085 733553 Pja2 praja ring finger ubiquitin ligase 2 gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20240321 MGI PMID:38379085 733553 Pja2 praja ring finger ubiquitin ligase 2 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20240321 MGI PMID:38379085 733553 Pja2 praja ring finger ubiquitin ligase 2 gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20240321 MGI PMID:38379085 733553 Pja2 praja ring finger ubiquitin ligase 2 gene MP:0014361 increased necroptotic process IAGP N RGD:5509061 20240321 MGI PMID:38379085 733558 Gpr27 G protein-coupled receptor 27 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201015 MGI PMID:32221326 733558 Gpr27 G protein-coupled receptor 27 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20201015 MGI PMID:32221326 733558 Gpr27 G protein-coupled receptor 27 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20201015 MGI PMID:32221326 733558 Gpr27 G protein-coupled receptor 27 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20201015 MGI PMID:32221326 733558 Gpr27 G protein-coupled receptor 27 gene MP:0010147 abnormal endocrine pancreas physiology IAGP N RGD:5509061 20201015 MGI PMID:32221326 733559 Agrp agouti related neuropeptide gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:23864684 733559 Agrp agouti related neuropeptide gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17097059 733559 Agrp agouti related neuropeptide gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22419158 733559 Agrp agouti related neuropeptide gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22941110 733559 Agrp agouti related neuropeptide gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:22941110 733559 Agrp agouti related neuropeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16254186 733559 Agrp agouti related neuropeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16330327 733559 Agrp agouti related neuropeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18272480 733559 Agrp agouti related neuropeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19160495 733559 Agrp agouti related neuropeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22232663 733559 Agrp agouti related neuropeptide gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22232663 733559 Agrp agouti related neuropeptide gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16330327 733559 Agrp agouti related neuropeptide gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:16254186 733559 Agrp agouti related neuropeptide gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:18272480 733559 Agrp agouti related neuropeptide gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22232663 733559 Agrp agouti related neuropeptide gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22419158 733559 Agrp agouti related neuropeptide gene MP:0001657 abnormal induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16254186 733559 Agrp agouti related neuropeptide gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:17097059 733559 Agrp agouti related neuropeptide gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:22419158 733559 Agrp agouti related neuropeptide gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12077332 733559 Agrp agouti related neuropeptide gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18272480 733559 Agrp agouti related neuropeptide gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19160495 733559 Agrp agouti related neuropeptide gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:23864684 733559 Agrp agouti related neuropeptide gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17097059 733559 Agrp agouti related neuropeptide gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23864684 733559 Agrp agouti related neuropeptide gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23864684 733559 Agrp agouti related neuropeptide gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16330327 733559 Agrp agouti related neuropeptide gene MP:0005111 hyperdipsia IAGP N RGD:5509061 20141003 MGI PMID:16254186 733559 Agrp agouti related neuropeptide gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19160495 733559 Agrp agouti related neuropeptide gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22232663 733559 Agrp agouti related neuropeptide gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:16330327 733559 Agrp agouti related neuropeptide gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:19160495 733559 Agrp agouti related neuropeptide gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:16330327 733559 Agrp agouti related neuropeptide gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:17097059 733559 Agrp agouti related neuropeptide gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:16330327 733559 Agrp agouti related neuropeptide gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:16330327 733559 Agrp agouti related neuropeptide gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:22232663 733559 Agrp agouti related neuropeptide gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19160495 733559 Agrp agouti related neuropeptide gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16330327 733559 Agrp agouti related neuropeptide gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22232663 733559 Agrp agouti related neuropeptide gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22941110 733559 Agrp agouti related neuropeptide gene MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22941110 733559 Agrp agouti related neuropeptide gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22941110 733559 Agrp agouti related neuropeptide gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23864684 733559 Agrp agouti related neuropeptide gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16330327 733559 Agrp agouti related neuropeptide gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22232663 733559 Agrp agouti related neuropeptide gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22941110 733559 Agrp agouti related neuropeptide gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16330327 733559 Agrp agouti related neuropeptide gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19160495 733559 Agrp agouti related neuropeptide gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:22419158 733559 Agrp agouti related neuropeptide gene MP:0010143 enhanced fertility IAGP N RGD:5509061 20141003 MGI PMID:22232663 733559 Agrp agouti related neuropeptide gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:23864684 733559 Agrp agouti related neuropeptide gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:16330327 733559 Agrp agouti related neuropeptide gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:19160495 733559 Agrp agouti related neuropeptide gene MP:0011016 increased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:16330327 733559 Agrp agouti related neuropeptide gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:17097059 733559 Agrp agouti related neuropeptide gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:17097059 733559 Agrp agouti related neuropeptide gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:18272480 733559 Agrp agouti related neuropeptide gene MP:0012575 increased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:23864684 733559 Agrp agouti related neuropeptide gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:19160495 733561 Rpl22 ribosomal protein L22 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:23990801 733561 Rpl22 ribosomal protein L22 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17555992 733561 Rpl22 ribosomal protein L22 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17555992 733561 Rpl22 ribosomal protein L22 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17555992 733561 Rpl22 ribosomal protein L22 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19666516 733561 Rpl22 ribosomal protein L22 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:17555992 733561 Rpl22 ribosomal protein L22 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23990801 733561 Rpl22 ribosomal protein L22 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17555992 733561 Rpl22 ribosomal protein L22 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23990801 733561 Rpl22 ribosomal protein L22 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17555992 733561 Rpl22 ribosomal protein L22 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:17555992 733561 Rpl22 ribosomal protein L22 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17555992 733561 Rpl22 ribosomal protein L22 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17555992 733561 Rpl22 ribosomal protein L22 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17555992 733564 Cpa1 carboxypeptidase A1, pancreatic gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20210204 MGI PMID:30045879 733564 Cpa1 carboxypeptidase A1, pancreatic gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17609113 733564 Cpa1 carboxypeptidase A1, pancreatic gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20210204 MGI PMID:30045879 733564 Cpa1 carboxypeptidase A1, pancreatic gene MP:0004247 small pancreas IAGP N RGD:5509061 20210204 MGI PMID:30045879 733564 Cpa1 carboxypeptidase A1, pancreatic gene MP:0008805 decreased circulating amylase level IAGP N RGD:5509061 20210204 MGI PMID:30045879 733564 Cpa1 carboxypeptidase A1, pancreatic gene MP:0008806 increased circulating amylase level IAGP N RGD:5509061 20210204 MGI PMID:30045879 733564 Cpa1 carboxypeptidase A1, pancreatic gene MP:0009109 decreased pancreas weight IAGP N RGD:5509061 20210204 MGI PMID:30045879 733564 Cpa1 carboxypeptidase A1, pancreatic gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20210204 MGI PMID:30045879 733564 Cpa1 carboxypeptidase A1, pancreatic gene MP:0009149 decreased pancreatic acinar cell number IAGP N RGD:5509061 20210204 MGI PMID:30045879 733564 Cpa1 carboxypeptidase A1, pancreatic gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20210204 MGI PMID:30045879 733564 Cpa1 carboxypeptidase A1, pancreatic gene MP:0013295 pancreas atrophy IAGP N RGD:5509061 20210204 MGI PMID:30045879 733564 Cpa1 carboxypeptidase A1, pancreatic gene MP:0030681 increased circulating hydroxyproline level IAGP N RGD:5509061 20210204 MGI PMID:30045879 733565 Oas1g 2'-5' oligoadenylate synthetase 1G gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20211021 MGI 733565 Oas1g 2'-5' oligoadenylate synthetase 1G gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733567 Tfam transcription factor A, mitochondrial gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:9916807 733567 Tfam transcription factor A, mitochondrial gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9500544 733567 Tfam transcription factor A, mitochondrial gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9916807 733567 Tfam transcription factor A, mitochondrial gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141030 MGI PMID:23386745 733567 Tfam transcription factor A, mitochondrial gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20160310 MGI PMID:22110743 733567 Tfam transcription factor A, mitochondrial gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20160310 MGI PMID:22110743 733567 Tfam transcription factor A, mitochondrial gene MP:0000648 absent sebaceous gland IAGP N RGD:5509061 20150813 MGI PMID:23386745 733567 Tfam transcription factor A, mitochondrial gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:17227870 733567 Tfam transcription factor A, mitochondrial gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17227870 733567 Tfam transcription factor A, mitochondrial gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20160310 MGI PMID:22110743 733567 Tfam transcription factor A, mitochondrial gene MP:0001105 abnormal PNS glial cell morphology IAGP N RGD:5509061 20160310 MGI PMID:22110743 733567 Tfam transcription factor A, mitochondrial gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141030 MGI PMID:23386745 733567 Tfam transcription factor A, mitochondrial gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:12417746 733567 Tfam transcription factor A, mitochondrial gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21768369 733567 Tfam transcription factor A, mitochondrial gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9500544 733567 Tfam transcription factor A, mitochondrial gene MP:0001265 decreased body size IAGP N RGD:5509061 20160310 MGI PMID:22110743 733567 Tfam transcription factor A, mitochondrial gene MP:0001270 distended abdomen IAGP N RGD:5509061 20160310 MGI PMID:22110743 733567 Tfam transcription factor A, mitochondrial gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:9500544 733567 Tfam transcription factor A, mitochondrial gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:21768369 733567 Tfam transcription factor A, mitochondrial gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17227870 733567 Tfam transcription factor A, mitochondrial gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17227870 733567 Tfam transcription factor A, mitochondrial gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:9916807 733567 Tfam transcription factor A, mitochondrial gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11062475 733567 Tfam transcription factor A, mitochondrial gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:9500544 733567 Tfam transcription factor A, mitochondrial gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9916807 733567 Tfam transcription factor A, mitochondrial gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160310 MGI PMID:22110743 733567 Tfam transcription factor A, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10737799 733567 Tfam transcription factor A, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11588181 733567 Tfam transcription factor A, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12417746 733567 Tfam transcription factor A, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17227870 733567 Tfam transcription factor A, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20141030 MGI PMID:23386745 733567 Tfam transcription factor A, mitochondrial gene MP:0002083 premature death IAGP N RGD:5509061 20160310 MGI PMID:22110743 733567 Tfam transcription factor A, mitochondrial gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:11588181 733567 Tfam transcription factor A, mitochondrial gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:11588181 733567 Tfam transcription factor A, mitochondrial gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20160310 MGI PMID:22110743 733567 Tfam transcription factor A, mitochondrial gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141030 MGI PMID:23386745 733567 Tfam transcription factor A, mitochondrial gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:10737799 733567 Tfam transcription factor A, mitochondrial gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:9916807 733567 Tfam transcription factor A, mitochondrial gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:10737799 733567 Tfam transcription factor A, mitochondrial gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:9916807 733567 Tfam transcription factor A, mitochondrial gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:10737799 733567 Tfam transcription factor A, mitochondrial gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:9916807 733567 Tfam transcription factor A, mitochondrial gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12417746 733567 Tfam transcription factor A, mitochondrial gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21768369 733567 Tfam transcription factor A, mitochondrial gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11062475 733567 Tfam transcription factor A, mitochondrial gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:11062475 733567 Tfam transcription factor A, mitochondrial gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:10737799 733567 Tfam transcription factor A, mitochondrial gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20141030 MGI PMID:23386745 733567 Tfam transcription factor A, mitochondrial gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11259653 733567 Tfam transcription factor A, mitochondrial gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:11588181 733567 Tfam transcription factor A, mitochondrial gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17227870 733567 Tfam transcription factor A, mitochondrial gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:17227870 733567 Tfam transcription factor A, mitochondrial gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:21768369 733567 Tfam transcription factor A, mitochondrial gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141030 MGI PMID:23386745 733567 Tfam transcription factor A, mitochondrial gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:9500544 733567 Tfam transcription factor A, mitochondrial gene MP:0004143 muscle hypertonia IAGP N RGD:5509061 20141003 MGI PMID:21768369 733567 Tfam transcription factor A, mitochondrial gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:17227870 733567 Tfam transcription factor A, mitochondrial gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:17227870 733567 Tfam transcription factor A, mitochondrial gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:21768369 733567 Tfam transcription factor A, mitochondrial gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:12417746 733567 Tfam transcription factor A, mitochondrial gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:9916807 733567 Tfam transcription factor A, mitochondrial gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:11259653 733567 Tfam transcription factor A, mitochondrial gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:11588181 733567 Tfam transcription factor A, mitochondrial gene MP:0005405 axon degeneration IAGP N RGD:5509061 20160310 MGI PMID:22110743 733567 Tfam transcription factor A, mitochondrial gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:17227870 733567 Tfam transcription factor A, mitochondrial gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:11062475 733567 Tfam transcription factor A, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:21768369 733567 Tfam transcription factor A, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141030 MGI PMID:23386745 733567 Tfam transcription factor A, mitochondrial gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11259653 733567 Tfam transcription factor A, mitochondrial gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141030 MGI PMID:23386745 733567 Tfam transcription factor A, mitochondrial gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141030 MGI PMID:23386745 733567 Tfam transcription factor A, mitochondrial gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20141030 MGI PMID:23386745 733567 Tfam transcription factor A, mitochondrial gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9916807 733567 Tfam transcription factor A, mitochondrial gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20160310 MGI PMID:22110743 733567 Tfam transcription factor A, mitochondrial gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20141030 MGI PMID:23386745 733567 Tfam transcription factor A, mitochondrial gene MP:0009174 absent pancreatic beta cells IAGP N RGD:5509061 20141003 MGI PMID:11062475 733567 Tfam transcription factor A, mitochondrial gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:12417746 733567 Tfam transcription factor A, mitochondrial gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141030 MGI PMID:23386745 733567 Tfam transcription factor A, mitochondrial gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:10737799 733567 Tfam transcription factor A, mitochondrial gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:11062475 733567 Tfam transcription factor A, mitochondrial gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:11259653 733567 Tfam transcription factor A, mitochondrial gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:11588181 733567 Tfam transcription factor A, mitochondrial gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:12417746 733567 Tfam transcription factor A, mitochondrial gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:11259653 733567 Tfam transcription factor A, mitochondrial gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9916807 733567 Tfam transcription factor A, mitochondrial gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10737799 733567 Tfam transcription factor A, mitochondrial gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9500544 733567 Tfam transcription factor A, mitochondrial gene MP:0011602 increased glutathione peroxidase activity IAGP N RGD:5509061 20141003 MGI PMID:11259653 733567 Tfam transcription factor A, mitochondrial gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:9500544 733567 Tfam transcription factor A, mitochondrial gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20141003 MGI PMID:9500544 733567 Tfam transcription factor A, mitochondrial gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20141003 MGI PMID:11062475 733567 Tfam transcription factor A, mitochondrial gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20141003 MGI PMID:9500544 733567 Tfam transcription factor A, mitochondrial gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20160310 MGI PMID:22110743 733567 Tfam transcription factor A, mitochondrial gene MP:0014387 decreased neuron mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:22110743 733568 P2ry12 purinergic receptor P2Y, G-protein coupled 12 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 733568 P2ry12 purinergic receptor P2Y, G-protein coupled 12 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:12897207 733568 P2ry12 purinergic receptor P2Y, G-protein coupled 12 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:11413167 733568 P2ry12 purinergic receptor P2Y, G-protein coupled 12 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:12897207 733568 P2ry12 purinergic receptor P2Y, G-protein coupled 12 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:11413167 733568 P2ry12 purinergic receptor P2Y, G-protein coupled 12 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:12897207 733568 P2ry12 purinergic receptor P2Y, G-protein coupled 12 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201001 MGI PMID:12897207 733570 Psen2 presenilin 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 733570 Psen2 presenilin 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:10557208 733570 Psen2 presenilin 2 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15525534 733570 Psen2 presenilin 2 gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:15525534 733570 Psen2 presenilin 2 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:15525534 733570 Psen2 presenilin 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 733570 Psen2 presenilin 2 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 733570 Psen2 presenilin 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:15148382 733570 Psen2 presenilin 2 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:10557208 733570 Psen2 presenilin 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15148382 733570 Psen2 presenilin 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20160407 MGI PMID:25741723 733570 Psen2 presenilin 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:15525534 733570 Psen2 presenilin 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:15525534 733570 Psen2 presenilin 2 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:15525534 733570 Psen2 presenilin 2 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15525534 733570 Psen2 presenilin 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15148382 733570 Psen2 presenilin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15525534 733570 Psen2 presenilin 2 gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15148382 733570 Psen2 presenilin 2 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:15148382 733570 Psen2 presenilin 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20160407 MGI PMID:25741723 733570 Psen2 presenilin 2 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15148382 733570 Psen2 presenilin 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:10557208 733570 Psen2 presenilin 2 gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:10557208 733570 Psen2 presenilin 2 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20230119 MGI 733570 Psen2 presenilin 2 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20160407 MGI PMID:25741723 733570 Psen2 presenilin 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230119 MGI 733570 Psen2 presenilin 2 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:15525534 733570 Psen2 presenilin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15525534 733570 Psen2 presenilin 2 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 733570 Psen2 presenilin 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10557208 733570 Psen2 presenilin 2 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230119 MGI 733570 Psen2 presenilin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10497236 733570 Psen2 presenilin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10557208 733570 Psen2 presenilin 2 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:15148382 733570 Psen2 presenilin 2 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:10557208 733570 Psen2 presenilin 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:15148382 733570 Psen2 presenilin 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20160407 MGI PMID:25741723 733570 Psen2 presenilin 2 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:10557208 733570 Psen2 presenilin 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:10557208 733570 Psen2 presenilin 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15148382 733570 Psen2 presenilin 2 gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20160407 MGI PMID:25741723 733570 Psen2 presenilin 2 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20160407 MGI PMID:25741723 733570 Psen2 presenilin 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20160407 MGI PMID:25741723 733570 Psen2 presenilin 2 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:10557208 733570 Psen2 presenilin 2 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:15525534 733570 Psen2 presenilin 2 gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:15525534 733570 Psen2 presenilin 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:10557208 733570 Psen2 presenilin 2 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:10557208 733570 Psen2 presenilin 2 gene MP:0004546 esophagus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15525534 733570 Psen2 presenilin 2 gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0005161 hematuria IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 733570 Psen2 presenilin 2 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:10557208 733570 Psen2 presenilin 2 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10557208 733570 Psen2 presenilin 2 gene MP:0008286 abnormal hippocampus molecular cell layer IAGP N RGD:5509061 20141003 MGI PMID:15148382 733570 Psen2 presenilin 2 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20160407 MGI PMID:25741723 733570 Psen2 presenilin 2 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:22496554 733570 Psen2 presenilin 2 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:15148382 733570 Psen2 presenilin 2 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:15148382 733570 Psen2 presenilin 2 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20160407 MGI PMID:25741723 733570 Psen2 presenilin 2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20160407 MGI PMID:25741723 733570 Psen2 presenilin 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20160407 MGI PMID:25741723 733570 Psen2 presenilin 2 gene MP:0010138 arteritis IAGP N RGD:5509061 20141003 MGI PMID:15128703 733570 Psen2 presenilin 2 gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:15525534 733570 Psen2 presenilin 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10557208 733570 Psen2 presenilin 2 gene MP:0011141 increased lung endothelial cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0013380 absent sebocyte IAGP N RGD:5509061 20141218 MGI PMID:15525534 733570 Psen2 presenilin 2 gene MP:0014473 increased pulmonary alveolus wall thickness IAGP N RGD:5509061 20240704 MGI PMID:10518543 733570 Psen2 presenilin 2 gene MP:0030002 increased lung apoptosis IAGP N RGD:5509061 20240704 MGI PMID:10518543 733572 Nlgn3 neuroligin 3 gene MP:0000062 increased bone mineral density IEA N RGD:5509061 20210128 MGI 733572 Nlgn3 neuroligin 3 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:19243448 733572 Nlgn3 neuroligin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16982420 733572 Nlgn3 neuroligin 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:17823315 733572 Nlgn3 neuroligin 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:19243448 733572 Nlgn3 neuroligin 3 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 733572 Nlgn3 neuroligin 3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20150917 MGI PMID:24995986 733572 Nlgn3 neuroligin 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20150917 MGI PMID:24995986 733572 Nlgn3 neuroligin 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19360662 733572 Nlgn3 neuroligin 3 gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20150917 MGI PMID:24995986 733572 Nlgn3 neuroligin 3 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20150917 MGI PMID:24995986 733572 Nlgn3 neuroligin 3 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20220421 MGI PMID:19243448 733572 Nlgn3 neuroligin 3 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17823315 733572 Nlgn3 neuroligin 3 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19360662 733572 Nlgn3 neuroligin 3 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:19360662 733572 Nlgn3 neuroligin 3 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:19360662 733572 Nlgn3 neuroligin 3 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:22983708 733572 Nlgn3 neuroligin 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19360662 733572 Nlgn3 neuroligin 3 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:22983708 733572 Nlgn3 neuroligin 3 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:22983708 733572 Nlgn3 neuroligin 3 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16982420 733572 Nlgn3 neuroligin 3 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:16982420 733572 Nlgn3 neuroligin 3 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:19360662 733572 Nlgn3 neuroligin 3 gene MP:0002068 abnormal parental behavior IAGP N RGD:5509061 20141003 MGI PMID:16982420 733572 Nlgn3 neuroligin 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17823315 733572 Nlgn3 neuroligin 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:16982420 733572 Nlgn3 neuroligin 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20160414 MGI PMID:26291161 733572 Nlgn3 neuroligin 3 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20220421 MGI PMID:24995986 733572 Nlgn3 neuroligin 3 gene MP:0002596 abnormal hematocrit IEA N RGD:5509061 20220519 MGI 733572 Nlgn3 neuroligin 3 gene MP:0002602 abnormal eosinophil cell number IEA N RGD:5509061 20220519 MGI 733572 Nlgn3 neuroligin 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:19360662 733572 Nlgn3 neuroligin 3 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:19360662 733572 Nlgn3 neuroligin 3 gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20141003 MGI PMID:19360662 733572 Nlgn3 neuroligin 3 gene MP:0002865 increased growth rate IAGP N RGD:5509061 20141003 MGI PMID:19360662 733572 Nlgn3 neuroligin 3 gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:21642956 733572 Nlgn3 neuroligin 3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:21642956 733572 Nlgn3 neuroligin 3 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17823315 733572 Nlgn3 neuroligin 3 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20160414 MGI PMID:26291161 733572 Nlgn3 neuroligin 3 gene MP:0003313 abnormal locomotor activation IEA N RGD:5509061 20220519 MGI 733572 Nlgn3 neuroligin 3 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:19360662 733572 Nlgn3 neuroligin 3 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:16982420 733572 Nlgn3 neuroligin 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21642956 733572 Nlgn3 neuroligin 3 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22983708 733572 Nlgn3 neuroligin 3 gene MP:0004997 increased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:22983708 733572 Nlgn3 neuroligin 3 gene MP:0005563 abnormal hemoglobin content IEA N RGD:5509061 20220519 MGI 733572 Nlgn3 neuroligin 3 gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:19243448 733572 Nlgn3 neuroligin 3 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20160414 MGI PMID:26291161 733572 Nlgn3 neuroligin 3 gene MP:0008820 abnormal blood uric acid level IEA N RGD:5509061 20211021 MGI 733572 Nlgn3 neuroligin 3 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20160414 MGI PMID:26291161 733572 Nlgn3 neuroligin 3 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19243448 733572 Nlgn3 neuroligin 3 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19243448 733572 Nlgn3 neuroligin 3 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20160414 MGI PMID:26291161 733572 Nlgn3 neuroligin 3 gene MP:0010066 abnormal red blood cell distribution width IEA N RGD:5509061 20220519 MGI 733572 Nlgn3 neuroligin 3 gene MP:0010746 abnormal pre-Botzinger complex physiology IAGP N RGD:5509061 20141003 MGI PMID:16982420 733572 Nlgn3 neuroligin 3 gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21642956 733572 Nlgn3 neuroligin 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16982420 733572 Nlgn3 neuroligin 3 gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:22983708 733572 Nlgn3 neuroligin 3 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20160414 MGI PMID:26291161 733572 Nlgn3 neuroligin 3 gene MP:0012314 enhanced learning IAGP N RGD:5509061 20150917 MGI PMID:24995986 733572 Nlgn3 neuroligin 3 gene MP:0012440 abnormal neutrophil cell number IEA N RGD:5509061 20220519 MGI 733572 Nlgn3 neuroligin 3 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:24995986 733572 Nlgn3 neuroligin 3 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:26291161 733572 Nlgn3 neuroligin 3 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:26291161 733572 Nlgn3 neuroligin 3 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:19243448 733572 Nlgn3 neuroligin 3 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:19360662 733572 Nlgn3 neuroligin 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:19243448 733572 Nlgn3 neuroligin 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:24995986 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16543498 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0000275 heart hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16543498 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16079292 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16543498 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16543498 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:16079292 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20201022 MGI 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:21674029 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20201022 MGI 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:21674029 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21674029 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:21674029 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:16079292 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:21674029 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20201022 MGI 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:15864812 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0002989 small kidney IEA N RGD:5509061 20201022 MGI 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18636119 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15864812 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16543498 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0003808 increased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:16079292 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:18636119 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:18794341 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16543498 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0003928 increased heart rate variability IAGP N RGD:5509061 20141003 MGI PMID:18794341 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0004068 dilated dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:16079292 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:18636119 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:16079292 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0004114 abnormal atrioventricular node morphology IAGP N RGD:5509061 20141003 MGI PMID:18794341 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:21674029 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:16079292 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:16079292 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:16543498 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18636119 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:21674029 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:15864812 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:15864812 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16079292 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16543498 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:18636119 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16543498 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:16079292 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16079292 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0006141 abnormal atrioventricular node conduction IAGP N RGD:5509061 20141003 MGI PMID:18794341 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:18636119 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:21674029 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16079292 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0009149 decreased pancreatic acinar cell number IAGP N RGD:5509061 20150611 MGI PMID:21674029 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0009164 exocrine pancreas atrophy IAGP N RGD:5509061 20141003 MGI PMID:21674029 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0010507 shortened RR interval IAGP N RGD:5509061 20141003 MGI PMID:18636119 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:18636119 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0010510 absent P wave IAGP N RGD:5509061 20141003 MGI PMID:18636119 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:18636119 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:21674029 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15864812 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16079292 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16543498 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18636119 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18794341 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0011646 abnormal sinoatrial valve morphology IAGP N RGD:5509061 20231221 MGI PMID:16543498 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0011647 absent sinoatrial valve IAGP N RGD:5509061 20231221 MGI PMID:16543498 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0013221 pancreatic acinar-to-ductal metaplasia IAGP N RGD:5509061 20150611 MGI PMID:21674029 733573 Cxadr coxsackie virus and adenovirus receptor gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20160310 MGI PMID:16079292 733574 Btc betacellulin, epidermal growth factor family member gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 733574 Btc betacellulin, epidermal growth factor family member gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 733574 Btc betacellulin, epidermal growth factor family member gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12773386 733574 Btc betacellulin, epidermal growth factor family member gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:12773386 733574 Btc betacellulin, epidermal growth factor family member gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12773386 733574 Btc betacellulin, epidermal growth factor family member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12773386 733574 Btc betacellulin, epidermal growth factor family member gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 733574 Btc betacellulin, epidermal growth factor family member gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12773386 733574 Btc betacellulin, epidermal growth factor family member gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20141003 MGI PMID:12773386 733574 Btc betacellulin, epidermal growth factor family member gene MP:0004063 dilated heart left atrium IAGP N RGD:5509061 20141003 MGI PMID:12773386 733574 Btc betacellulin, epidermal growth factor family member gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12773386 733574 Btc betacellulin, epidermal growth factor family member gene MP:0010591 enlarged aortic valve IAGP N RGD:5509061 20141003 MGI PMID:12773386 733574 Btc betacellulin, epidermal growth factor family member gene MP:0010600 enlarged pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:12773386 733574 Btc betacellulin, epidermal growth factor family member gene MP:0031570 enlarged atrioventricular valve IAGP N RGD:5509061 20240125 MGI PMID:12773386 733574 Btc betacellulin, epidermal growth factor family member gene MP:0031580 enlarged semilunar valve IAGP N RGD:5509061 20240125 MGI PMID:12773386 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20200618 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:22252315 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:14726372 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:14726372 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:22252315 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:22252315 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0004892 increased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:22252315 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22252315 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160804 MGI 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:22252315 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:9271584 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:14726372 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:14726372 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:14726372 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:22252315 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0011722 abnormal ossification involved in bone maturation IAGP N RGD:5509061 20141003 MGI PMID:22590589 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0014440 increased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:22000926 733576 Ptpn2 protein tyrosine phosphatase, non-receptor type 2 gene MP:0030984 increased circulating osteocalcin level IAGP N RGD:5509061 20201002 MGI PMID:22252315 733578 Avpi1 arginine vasopressin-induced 1 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20220811 MGI 733578 Avpi1 arginine vasopressin-induced 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 733578 Avpi1 arginine vasopressin-induced 1 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20201022 MGI 733582 Artn artemin gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12160745 733582 Artn artemin gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12160745 733582 Artn artemin gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:12160745 733582 Artn artemin gene MP:0001025 abnormal sympathetic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12160745 733582 Artn artemin gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12160745 733582 Artn artemin gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:12160745 733584 Srpx sushi-repeat-containing protein gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17088259 733584 Srpx sushi-repeat-containing protein gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17088259 733584 Srpx sushi-repeat-containing protein gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17088259 733584 Srpx sushi-repeat-containing protein gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17088259 733584 Srpx sushi-repeat-containing protein gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17088259 733584 Srpx sushi-repeat-containing protein gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17088259 733584 Srpx sushi-repeat-containing protein gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17088259 733584 Srpx sushi-repeat-containing protein gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17088259 733585 Pter phosphotriesterase related gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 733587 Rgs7 regulator of G protein signaling 7 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22371490 733587 Rgs7 regulator of G protein signaling 7 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:22371490 733587 Rgs7 regulator of G protein signaling 7 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20111116 MGI 733587 Rgs7 regulator of G protein signaling 7 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20111116 MGI 733587 Rgs7 regulator of G protein signaling 7 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:22547806 733587 Rgs7 regulator of G protein signaling 7 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22371490 733587 Rgs7 regulator of G protein signaling 7 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19535587 733587 Rgs7 regulator of G protein signaling 7 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22371490 733587 Rgs7 regulator of G protein signaling 7 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22547806 733587 Rgs7 regulator of G protein signaling 7 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22371490 733587 Rgs7 regulator of G protein signaling 7 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20111116 MGI 733587 Rgs7 regulator of G protein signaling 7 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19535587 733587 Rgs7 regulator of G protein signaling 7 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22371490 733587 Rgs7 regulator of G protein signaling 7 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:22371490 733589 Barhl1 BarH like homeobox 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:12091321 733589 Barhl1 BarH like homeobox 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:12091321 733589 Barhl1 BarH like homeobox 1 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12091321 733589 Barhl1 BarH like homeobox 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12091321 733589 Barhl1 BarH like homeobox 1 gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12091321 733589 Barhl1 BarH like homeobox 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12091321 733591 Tecr trans-2,3-enoyl-CoA reductase gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20211021 MGI 733591 Tecr trans-2,3-enoyl-CoA reductase gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210520 MGI 733591 Tecr trans-2,3-enoyl-CoA reductase gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210520 MGI 733591 Tecr trans-2,3-enoyl-CoA reductase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733593 Stxbp2 syntaxin binding protein 2 gene MP:0000358 abnormal cell morphology IEA N RGD:5509061 20141003 MGI 733593 Stxbp2 syntaxin binding protein 2 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:22694344 733593 Stxbp2 syntaxin binding protein 2 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:22694344 733593 Stxbp2 syntaxin binding protein 2 gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:22694344 733593 Stxbp2 syntaxin binding protein 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22694344 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20160505 MGI PMID:25731822 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20160505 MGI PMID:25731822 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20160505 MGI PMID:25731822 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20160505 MGI PMID:25731822 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20160505 MGI PMID:25731822 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20160505 MGI PMID:25731822 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20160505 MGI PMID:25731822 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0008335 decreased gonadotroph cell number IAGP N RGD:5509061 20160505 MGI PMID:25731822 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0009012 short diestrus IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0009020 prolonged metestrus IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20190919 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:26977770 733598 Nsmf NMDA receptor synaptonuclear signaling and neuronal migration factor gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:26977770 733599 Ptk2b PTK2 protein tyrosine kinase 2 beta gene MP:0001934 increased litter size IAGP N RGD:5509061 20230810 MGI PMID:32608523 733599 Ptk2b PTK2 protein tyrosine kinase 2 beta gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12960403 733599 Ptk2b PTK2 protein tyrosine kinase 2 beta gene MP:0002678 increased follicle recruitment IAGP N RGD:5509061 20230810 MGI PMID:32608523 733599 Ptk2b PTK2 protein tyrosine kinase 2 beta gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:17698736 733599 Ptk2b PTK2 protein tyrosine kinase 2 beta gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:17698736 733599 Ptk2b PTK2 protein tyrosine kinase 2 beta gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12960403 733599 Ptk2b PTK2 protein tyrosine kinase 2 beta gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17698736 733599 Ptk2b PTK2 protein tyrosine kinase 2 beta gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:12960403 733599 Ptk2b PTK2 protein tyrosine kinase 2 beta gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:17698736 733601 Pnliprp2 pancreatic lipase-related protein 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9813028 733601 Pnliprp2 pancreatic lipase-related protein 2 gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:9813028 733601 Pnliprp2 pancreatic lipase-related protein 2 gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:9813028 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170209 MGI 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0003156 abnormal leukocyte migration IEA N RGD:5509061 20111116 MGI 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0004056 abnormal myocardium compact layer morphology IEA N RGD:5509061 20170209 MGI 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0005505 thrombocytosis IEA N RGD:5509061 20201022 MGI 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0008129 absent brain internal capsule IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0008457 abnormal cortical intermediate zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0009026 abnormal brain pia mater morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0009027 abnormal subarachnoid space morphology IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20170209 MGI 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20170209 MGI 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20170209 MGI 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0011724 ectopic cortical neuron IAGP N RGD:5509061 20141003 MGI PMID:17988629 733603 Evl Ena-vasodilator stimulated phosphoprotein gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20190502 MGI 733604 Apoe apolipoprotein E gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18480287 733604 Apoe apolipoprotein E gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10938015 733604 Apoe apolipoprotein E gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11160157 733604 Apoe apolipoprotein E gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11726538 733604 Apoe apolipoprotein E gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12638732 733604 Apoe apolipoprotein E gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12765335 733604 Apoe apolipoprotein E gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19481534 733604 Apoe apolipoprotein E gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22441102 733604 Apoe apolipoprotein E gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9598833 733604 Apoe apolipoprotein E gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 733604 Apoe apolipoprotein E gene MP:0000181 abnormal circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:1423598 733604 Apoe apolipoprotein E gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10655544 733604 Apoe apolipoprotein E gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11792702 733604 Apoe apolipoprotein E gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12454276 733604 Apoe apolipoprotein E gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12765335 733604 Apoe apolipoprotein E gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:1411543 733604 Apoe apolipoprotein E gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14563650 733604 Apoe apolipoprotein E gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15304490 733604 Apoe apolipoprotein E gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15840700 733604 Apoe apolipoprotein E gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18048852 733604 Apoe apolipoprotein E gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12235184 733604 Apoe apolipoprotein E gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14739216 733604 Apoe apolipoprotein E gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9218423 733604 Apoe apolipoprotein E gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10359567 733604 Apoe apolipoprotein E gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10614672 733604 Apoe apolipoprotein E gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11893779 733604 Apoe apolipoprotein E gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:1411543 733604 Apoe apolipoprotein E gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21149301 733604 Apoe apolipoprotein E gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8962133 733604 Apoe apolipoprotein E gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9294211 733604 Apoe apolipoprotein E gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 733604 Apoe apolipoprotein E gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9218423 733604 Apoe apolipoprotein E gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11045969 733604 Apoe apolipoprotein E gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11861300 733604 Apoe apolipoprotein E gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21779871 733604 Apoe apolipoprotein E gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20161020 MGI PMID:19858416 733604 Apoe apolipoprotein E gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18165355 733604 Apoe apolipoprotein E gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0000231 hypertension IAGP N RGD:5509061 20170209 MGI PMID:18160459 733604 Apoe apolipoprotein E gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:11045969 733604 Apoe apolipoprotein E gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:11861300 733604 Apoe apolipoprotein E gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:10666072 733604 Apoe apolipoprotein E gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:12538437 733604 Apoe apolipoprotein E gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:19347044 733604 Apoe apolipoprotein E gene MP:0000256 echinocytosis IAGP N RGD:5509061 20141003 MGI PMID:11861300 733604 Apoe apolipoprotein E gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15297377 733604 Apoe apolipoprotein E gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:24082102 733604 Apoe apolipoprotein E gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:10614672 733604 Apoe apolipoprotein E gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16840715 733604 Apoe apolipoprotein E gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:19023427 733604 Apoe apolipoprotein E gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:19139386 733604 Apoe apolipoprotein E gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15297377 733604 Apoe apolipoprotein E gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:15031124 733604 Apoe apolipoprotein E gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:10777503 733604 Apoe apolipoprotein E gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:10087291 733604 Apoe apolipoprotein E gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:10777503 733604 Apoe apolipoprotein E gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:14741101 733604 Apoe apolipoprotein E gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:15566430 733604 Apoe apolipoprotein E gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10684907 733604 Apoe apolipoprotein E gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:9541503 733604 Apoe apolipoprotein E gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23577189 733604 Apoe apolipoprotein E gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7498401 733604 Apoe apolipoprotein E gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:7498401 733604 Apoe apolipoprotein E gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:10777503 733604 Apoe apolipoprotein E gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:10777503 733604 Apoe apolipoprotein E gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:10777503 733604 Apoe apolipoprotein E gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:11726538 733604 Apoe apolipoprotein E gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10777503 733604 Apoe apolipoprotein E gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:10777503 733604 Apoe apolipoprotein E gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:10777503 733604 Apoe apolipoprotein E gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:18344414 733604 Apoe apolipoprotein E gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:9294211 733604 Apoe apolipoprotein E gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:10975863 733604 Apoe apolipoprotein E gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19139386 733604 Apoe apolipoprotein E gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0001260 increased body weight IAGP N RGD:5509061 20170420 MGI PMID:9202070 733604 Apoe apolipoprotein E gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:21779871 733604 Apoe apolipoprotein E gene MP:0001261 obese IAGP N RGD:5509061 20170209 MGI PMID:18160459 733604 Apoe apolipoprotein E gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10614672 733604 Apoe apolipoprotein E gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10666072 733604 Apoe apolipoprotein E gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11045969 733604 Apoe apolipoprotein E gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15353487 733604 Apoe apolipoprotein E gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15914123 733604 Apoe apolipoprotein E gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17275002 733604 Apoe apolipoprotein E gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161020 MGI PMID:19858416 733604 Apoe apolipoprotein E gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170420 MGI PMID:9202070 733604 Apoe apolipoprotein E gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:18572164 733604 Apoe apolipoprotein E gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:16043866 733604 Apoe apolipoprotein E gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:16079201 733604 Apoe apolipoprotein E gene MP:0001337 dry eyes IAGP N RGD:5509061 20141003 MGI PMID:10777503 733604 Apoe apolipoprotein E gene MP:0001345 Meibomian gland atrophy IAGP N RGD:5509061 20141003 MGI PMID:10777503 733604 Apoe apolipoprotein E gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10684907 733604 Apoe apolipoprotein E gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15708438 733604 Apoe apolipoprotein E gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:11866033 733604 Apoe apolipoprotein E gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:11476599 733604 Apoe apolipoprotein E gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:11476599 733604 Apoe apolipoprotein E gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:11476599 733604 Apoe apolipoprotein E gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20220421 MGI PMID:18572260 733604 Apoe apolipoprotein E gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:10684907 733604 Apoe apolipoprotein E gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11476599 733604 Apoe apolipoprotein E gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12220566 733604 Apoe apolipoprotein E gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:9724804 733604 Apoe apolipoprotein E gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15708438 733604 Apoe apolipoprotein E gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:11476599 733604 Apoe apolipoprotein E gene MP:0001499 abnormal kindling response IAGP N RGD:5509061 20141003 MGI PMID:9607706 733604 Apoe apolipoprotein E gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:15647822 733604 Apoe apolipoprotein E gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:22862945 733604 Apoe apolipoprotein E gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:10359567 733604 Apoe apolipoprotein E gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:10772649 733604 Apoe apolipoprotein E gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:10938015 733604 Apoe apolipoprotein E gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:11076954 733604 Apoe apolipoprotein E gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:17296788 733604 Apoe apolipoprotein E gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:9218423 733604 Apoe apolipoprotein E gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:9649566 733604 Apoe apolipoprotein E gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:12454276 733604 Apoe apolipoprotein E gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:19481534 733604 Apoe apolipoprotein E gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:22441102 733604 Apoe apolipoprotein E gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:23383297 733604 Apoe apolipoprotein E gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:9649566 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10359567 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11076954 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11726538 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11792702 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12235184 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12454276 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12538880 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12730087 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12969990 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:1411543 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14563650 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15304490 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15840700 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17275002 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19023427 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19481534 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21779871 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23103473 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23999430 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9240444 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9294211 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9598833 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9649566 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170209 MGI PMID:18160459 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170420 MGI PMID:9202070 733604 Apoe apolipoprotein E gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20230810 MGI PMID:36073366 733604 Apoe apolipoprotein E gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20170209 MGI PMID:18160459 733604 Apoe apolipoprotein E gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10359567 733604 Apoe apolipoprotein E gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12235184 733604 Apoe apolipoprotein E gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12538880 733604 Apoe apolipoprotein E gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15304490 733604 Apoe apolipoprotein E gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15840700 733604 Apoe apolipoprotein E gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17275002 733604 Apoe apolipoprotein E gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18048852 733604 Apoe apolipoprotein E gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21149301 733604 Apoe apolipoprotein E gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7840811 733604 Apoe apolipoprotein E gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20170413 MGI PMID:26368306 733604 Apoe apolipoprotein E gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20170420 MGI PMID:9202070 733604 Apoe apolipoprotein E gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21779871 733604 Apoe apolipoprotein E gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20170209 MGI PMID:18160459 733604 Apoe apolipoprotein E gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:14739216 733604 Apoe apolipoprotein E gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12746502 733604 Apoe apolipoprotein E gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20220106 MGI PMID:30773021 733604 Apoe apolipoprotein E gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11045969 733604 Apoe apolipoprotein E gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:1423598 733604 Apoe apolipoprotein E gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:18725890 733604 Apoe apolipoprotein E gene MP:0001744 hypersecretion of corticosterone IAGP N RGD:5509061 20141003 MGI PMID:10684907 733604 Apoe apolipoprotein E gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:15708438 733604 Apoe apolipoprotein E gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:10744782 733604 Apoe apolipoprotein E gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:21779871 733604 Apoe apolipoprotein E gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:15297377 733604 Apoe apolipoprotein E gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:23577189 733604 Apoe apolipoprotein E gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12746502 733604 Apoe apolipoprotein E gene MP:0001863 blood vessel inflammation IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0001863 blood vessel inflammation IAGP N RGD:5509061 20141003 MGI PMID:23999430 733604 Apoe apolipoprotein E gene MP:0001876 decreased inflammatory response IEA N RGD:5509061 20220811 MGI 733604 Apoe apolipoprotein E gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20141003 MGI PMID:18344414 733604 Apoe apolipoprotein E gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20141003 MGI PMID:11476599 733604 Apoe apolipoprotein E gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18725890 733604 Apoe apolipoprotein E gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21779871 733604 Apoe apolipoprotein E gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20170209 MGI PMID:18160459 733604 Apoe apolipoprotein E gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10087291 733604 Apoe apolipoprotein E gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11726538 733604 Apoe apolipoprotein E gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12746502 733604 Apoe apolipoprotein E gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15914123 733604 Apoe apolipoprotein E gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24082102 733604 Apoe apolipoprotein E gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9294211 733604 Apoe apolipoprotein E gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9302276 733604 Apoe apolipoprotein E gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10777503 733604 Apoe apolipoprotein E gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11076954 733604 Apoe apolipoprotein E gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11095717 733604 Apoe apolipoprotein E gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11893779 733604 Apoe apolipoprotein E gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7840811 733604 Apoe apolipoprotein E gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9218423 733604 Apoe apolipoprotein E gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9649566 733604 Apoe apolipoprotein E gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:10683374 733604 Apoe apolipoprotein E gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:21779871 733604 Apoe apolipoprotein E gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10655544 733604 Apoe apolipoprotein E gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0002164 abnormal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:10684907 733604 Apoe apolipoprotein E gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18480287 733604 Apoe apolipoprotein E gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:12105373 733604 Apoe apolipoprotein E gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15096455 733604 Apoe apolipoprotein E gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20230824 MGI PMID:33762433 733604 Apoe apolipoprotein E gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:10366621 733604 Apoe apolipoprotein E gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:9724804 733604 Apoe apolipoprotein E gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:18344414 733604 Apoe apolipoprotein E gene MP:0002323 decreased susceptibility to hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:11076954 733604 Apoe apolipoprotein E gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17296788 733604 Apoe apolipoprotein E gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:17296788 733604 Apoe apolipoprotein E gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:15567863 733604 Apoe apolipoprotein E gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:15781238 733604 Apoe apolipoprotein E gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11861300 733604 Apoe apolipoprotein E gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10772649 733604 Apoe apolipoprotein E gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:14597759 733604 Apoe apolipoprotein E gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15567863 733604 Apoe apolipoprotein E gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:19023427 733604 Apoe apolipoprotein E gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:18325838 733604 Apoe apolipoprotein E gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:20026782 733604 Apoe apolipoprotein E gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10744782 733604 Apoe apolipoprotein E gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:12765335 733604 Apoe apolipoprotein E gene MP:0002626 increased heart rate IAGP N RGD:5509061 20240912 MGI PMID:35653516 733604 Apoe apolipoprotein E gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:11861300 733604 Apoe apolipoprotein E gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:11861300 733604 Apoe apolipoprotein E gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10359567 733604 Apoe apolipoprotein E gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10772649 733604 Apoe apolipoprotein E gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14739216 733604 Apoe apolipoprotein E gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15304490 733604 Apoe apolipoprotein E gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15353487 733604 Apoe apolipoprotein E gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19318355 733604 Apoe apolipoprotein E gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21149301 733604 Apoe apolipoprotein E gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9743578 733604 Apoe apolipoprotein E gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:10744782 733604 Apoe apolipoprotein E gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20141003 MGI PMID:9743578 733604 Apoe apolipoprotein E gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:11468208 733604 Apoe apolipoprotein E gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:9724804 733604 Apoe apolipoprotein E gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16043866 733604 Apoe apolipoprotein E gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:12220566 733604 Apoe apolipoprotein E gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:11045969 733604 Apoe apolipoprotein E gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:24082102 733604 Apoe apolipoprotein E gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12364322 733604 Apoe apolipoprotein E gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19347044 733604 Apoe apolipoprotein E gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0002865 increased growth rate IAGP N RGD:5509061 20141003 MGI PMID:10772649 733604 Apoe apolipoprotein E gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:18493081 733604 Apoe apolipoprotein E gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:11861300 733604 Apoe apolipoprotein E gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:7498401 733604 Apoe apolipoprotein E gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15353487 733604 Apoe apolipoprotein E gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0002964 aortic elastic tissue lesions IAGP N RGD:5509061 20141003 MGI PMID:9398846 733604 Apoe apolipoprotein E gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17138939 733604 Apoe apolipoprotein E gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:23383297 733604 Apoe apolipoprotein E gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:19347044 733604 Apoe apolipoprotein E gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:15031124 733604 Apoe apolipoprotein E gene MP:0003075 abnormal response to CNS ischemic injury IAGP N RGD:5509061 20141003 MGI PMID:12638732 733604 Apoe apolipoprotein E gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:15031124 733604 Apoe apolipoprotein E gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11468208 733604 Apoe apolipoprotein E gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:10666072 733604 Apoe apolipoprotein E gene MP:0003192 increased cholesterol efflux IAGP N RGD:5509061 20170413 MGI PMID:26368306 733604 Apoe apolipoprotein E gene MP:0003192 increased cholesterol efflux IAGP N RGD:5509061 20201002 MGI PMID:31102955 733604 Apoe apolipoprotein E gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:11950276 733604 Apoe apolipoprotein E gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:12451108 733604 Apoe apolipoprotein E gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:12969990 733604 Apoe apolipoprotein E gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:14741101 733604 Apoe apolipoprotein E gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:15772340 733604 Apoe apolipoprotein E gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:16079201 733604 Apoe apolipoprotein E gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:18202749 733604 Apoe apolipoprotein E gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:18480287 733604 Apoe apolipoprotein E gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:22492035 733604 Apoe apolipoprotein E gene MP:0003348 hypopituitarism IAGP N RGD:5509061 20141003 MGI PMID:10684907 733604 Apoe apolipoprotein E gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:11045969 733604 Apoe apolipoprotein E gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:10366621 733604 Apoe apolipoprotein E gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:9724804 733604 Apoe apolipoprotein E gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:16908765 733604 Apoe apolipoprotein E gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:9547235 733604 Apoe apolipoprotein E gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:12633754 733604 Apoe apolipoprotein E gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:15550530 733604 Apoe apolipoprotein E gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:17549254 733604 Apoe apolipoprotein E gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:19023427 733604 Apoe apolipoprotein E gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220106 MGI PMID:30773021 733604 Apoe apolipoprotein E gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:10087291 733604 Apoe apolipoprotein E gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:10772649 733604 Apoe apolipoprotein E gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:10777503 733604 Apoe apolipoprotein E gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:11160157 733604 Apoe apolipoprotein E gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:11726538 733604 Apoe apolipoprotein E gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:11866033 733604 Apoe apolipoprotein E gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:9358763 733604 Apoe apolipoprotein E gene MP:0003692 xanthoma IAGP N RGD:5509061 20141003 MGI PMID:9649566 733604 Apoe apolipoprotein E gene MP:0003692 xanthoma IAGP N RGD:5509061 20171102 MGI PMID:7772082 733604 Apoe apolipoprotein E gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:18325838 733604 Apoe apolipoprotein E gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11431458 733604 Apoe apolipoprotein E gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:15647822 733604 Apoe apolipoprotein E gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12569158 733604 Apoe apolipoprotein E gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15596719 733604 Apoe apolipoprotein E gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:9732872 733604 Apoe apolipoprotein E gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20151231 MGI PMID:22939356 733604 Apoe apolipoprotein E gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20210617 MGI PMID:19139386 733604 Apoe apolipoprotein E gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20230810 MGI PMID:36073366 733604 Apoe apolipoprotein E gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15746435 733604 Apoe apolipoprotein E gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19959238 733604 Apoe apolipoprotein E gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23999430 733604 Apoe apolipoprotein E gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20160630 MGI PMID:25278290 733604 Apoe apolipoprotein E gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:9724804 733604 Apoe apolipoprotein E gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:9743578 733604 Apoe apolipoprotein E gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:15746435 733604 Apoe apolipoprotein E gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:23383297 733604 Apoe apolipoprotein E gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20151231 MGI PMID:22939356 733604 Apoe apolipoprotein E gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0003897 abnormal ST segment IAGP N RGD:5509061 20141003 MGI PMID:15031124 733604 Apoe apolipoprotein E gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:10683374 733604 Apoe apolipoprotein E gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17138939 733604 Apoe apolipoprotein E gene MP:0003947 abnormal cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:12969990 733604 Apoe apolipoprotein E gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:17275002 733604 Apoe apolipoprotein E gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:18725890 733604 Apoe apolipoprotein E gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:19481534 733604 Apoe apolipoprotein E gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:22441102 733604 Apoe apolipoprotein E gene MP:0003950 abnormal plasma membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11930145 733604 Apoe apolipoprotein E gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20220106 MGI PMID:30773021 733604 Apoe apolipoprotein E gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10359567 733604 Apoe apolipoprotein E gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12235184 733604 Apoe apolipoprotein E gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12454276 733604 Apoe apolipoprotein E gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20170420 MGI PMID:9202070 733604 Apoe apolipoprotein E gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10359567 733604 Apoe apolipoprotein E gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:11893779 733604 Apoe apolipoprotein E gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:15304490 733604 Apoe apolipoprotein E gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:9169506 733604 Apoe apolipoprotein E gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10772649 733604 Apoe apolipoprotein E gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23103473 733604 Apoe apolipoprotein E gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20240523 MGI PMID:32686880 733604 Apoe apolipoprotein E gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10975863 733604 Apoe apolipoprotein E gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23383297 733604 Apoe apolipoprotein E gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20201002 MGI PMID:31102955 733604 Apoe apolipoprotein E gene MP:0003991 arteriosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11045969 733604 Apoe apolipoprotein E gene MP:0004044 aortic dissection IAGP N RGD:5509061 20141003 MGI PMID:11468208 733604 Apoe apolipoprotein E gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15914123 733604 Apoe apolipoprotein E gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:24082102 733604 Apoe apolipoprotein E gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15653570 733604 Apoe apolipoprotein E gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:15647822 733604 Apoe apolipoprotein E gene MP:0004153 increased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0004254 cerebral amyloid angiopathy IAGP N RGD:5509061 20141003 MGI PMID:15772340 733604 Apoe apolipoprotein E gene MP:0004308 abnormal basilar membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0004629 abnormal spiral modiolar artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0004630 spiral modiolar artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:18325838 733604 Apoe apolipoprotein E gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9607706 733604 Apoe apolipoprotein E gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:10655544 733604 Apoe apolipoprotein E gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20141003 MGI PMID:15567863 733604 Apoe apolipoprotein E gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20141003 MGI PMID:15596719 733604 Apoe apolipoprotein E gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:18325838 733604 Apoe apolipoprotein E gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:23577189 733604 Apoe apolipoprotein E gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:18325838 733604 Apoe apolipoprotein E gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11468208 733604 Apoe apolipoprotein E gene MP:0004879 decreased systemic vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:11045969 733604 Apoe apolipoprotein E gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:19481534 733604 Apoe apolipoprotein E gene MP:0004894 uterus atrophy IAGP N RGD:5509061 20141003 MGI PMID:11160157 733604 Apoe apolipoprotein E gene MP:0004904 increased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:10614672 733604 Apoe apolipoprotein E gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:10744782 733604 Apoe apolipoprotein E gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23577189 733604 Apoe apolipoprotein E gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:15647822 733604 Apoe apolipoprotein E gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18325838 733604 Apoe apolipoprotein E gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17138939 733604 Apoe apolipoprotein E gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:18572164 733604 Apoe apolipoprotein E gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17296788 733604 Apoe apolipoprotein E gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:15031124 733604 Apoe apolipoprotein E gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:16864727 733604 Apoe apolipoprotein E gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11468208 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10359567 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10655544 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11138930 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11792702 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12454276 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:1411543 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:1423598 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14563650 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15304490 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17275002 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18048852 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22441102 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7840811 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 733604 Apoe apolipoprotein E gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20170420 MGI PMID:9202070 733604 Apoe apolipoprotein E gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10359567 733604 Apoe apolipoprotein E gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12765335 733604 Apoe apolipoprotein E gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14739216 733604 Apoe apolipoprotein E gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14976060 733604 Apoe apolipoprotein E gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22441102 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10087291 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10488949 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10655544 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10712412 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10777503 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10938015 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11076954 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11726538 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11792702 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11866033 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11893779 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12177238 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12454276 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12730087 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12969990 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:1411543 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:1423598 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14563650 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15304490 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15550530 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15566430 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15781238 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15840700 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17275002 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18156214 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18325838 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18464897 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19481534 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21779871 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22441102 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23103473 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23577189 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23999430 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7498401 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7581381 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7840811 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9069289 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9137093 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9169506 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9218423 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9294211 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9598833 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9649566 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20151001 MGI PMID:8656070 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 733604 Apoe apolipoprotein E gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20170420 MGI PMID:9202070 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10614672 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12235184 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12364322 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12538880 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12638732 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14739216 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15353487 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15914123 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17483449 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19318355 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8962133 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9598833 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20170420 MGI PMID:9202070 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20171116 MGI PMID:26586440 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20230810 MGI PMID:36073366 733604 Apoe apolipoprotein E gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20240704 MGI PMID:9240444 733604 Apoe apolipoprotein E gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16079201 733604 Apoe apolipoprotein E gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:16079201 733604 Apoe apolipoprotein E gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:21779871 733604 Apoe apolipoprotein E gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11893779 733604 Apoe apolipoprotein E gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14976060 733604 Apoe apolipoprotein E gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19723498 733604 Apoe apolipoprotein E gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7581381 733604 Apoe apolipoprotein E gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20170420 MGI PMID:9202070 733604 Apoe apolipoprotein E gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15353487 733604 Apoe apolipoprotein E gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18725890 733604 Apoe apolipoprotein E gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20170209 MGI PMID:18160459 733604 Apoe apolipoprotein E gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:1423598 733604 Apoe apolipoprotein E gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18048852 733604 Apoe apolipoprotein E gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:15653570 733604 Apoe apolipoprotein E gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:10683374 733604 Apoe apolipoprotein E gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12177238 733604 Apoe apolipoprotein E gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:23577189 733604 Apoe apolipoprotein E gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21779871 733604 Apoe apolipoprotein E gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16462940 733604 Apoe apolipoprotein E gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:10087291 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:10666072 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:10683374 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:10712412 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:10938015 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:10975863 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:11045969 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:11095717 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:11160157 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:11726538 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:12454276 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:12633754 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:12746502 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:1411543 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:14597759 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15031124 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15304490 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15308551 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15550530 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15567863 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15653570 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:15781238 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:16371425 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:16840715 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17038633 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17068284 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17138939 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17483449 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17549254 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17641228 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:18988889 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:19048083 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:21779871 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:23577189 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:24082102 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:7840811 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:9069289 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:9137093 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:9294211 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:9649566 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20151001 MGI PMID:8656070 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20151231 MGI PMID:22939356 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20170209 MGI PMID:18160459 733604 Apoe apolipoprotein E gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20170420 MGI PMID:9202070 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:10359567 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:10683374 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11160157 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11468208 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11701467 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11866033 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12765335 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:1423598 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:14739216 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15096455 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17038633 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17916774 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18048852 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18325838 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18464897 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19723498 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19959238 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:20026782 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:21149301 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:22441102 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:23999430 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9218423 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9358763 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9649566 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20160630 MGI PMID:25278290 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20161020 MGI PMID:19858416 733604 Apoe apolipoprotein E gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20170420 MGI PMID:9202070 733604 Apoe apolipoprotein E gene MP:0005340 abnormal susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:14670837 733604 Apoe apolipoprotein E gene MP:0005340 abnormal susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15249654 733604 Apoe apolipoprotein E gene MP:0005340 abnormal susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19684185 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:10359567 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:10772649 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:10938015 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11581304 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12364322 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12538880 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12569158 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12600915 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:12730087 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:14563650 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:14976060 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15304490 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15353487 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15567863 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15596719 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15746435 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15914123 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16043658 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16908765 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17275002 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18156214 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18165355 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19023427 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19139386 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19347044 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19959238 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:22441102 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:22772436 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:23372835 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:23383297 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9137093 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9169506 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9398846 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:9732872 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20160804 MGI PMID:25872946 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20170413 MGI PMID:26368306 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20170420 MGI PMID:9202070 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20171116 MGI PMID:26586440 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20201002 MGI PMID:31102955 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20201217 MGI PMID:31163988 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20210617 MGI PMID:14597759 733604 Apoe apolipoprotein E gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20230810 MGI PMID:36073366 733604 Apoe apolipoprotein E gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20171116 MGI PMID:26586440 733604 Apoe apolipoprotein E gene MP:0005412 vascular stenosis IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:10938015 733604 Apoe apolipoprotein E gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:11893779 733604 Apoe apolipoprotein E gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:14739216 733604 Apoe apolipoprotein E gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:23999430 733604 Apoe apolipoprotein E gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20240523 MGI PMID:32686880 733604 Apoe apolipoprotein E gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:18344414 733604 Apoe apolipoprotein E gene MP:0005489 vascular smooth muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15653570 733604 Apoe apolipoprotein E gene MP:0005489 vascular smooth muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19959238 733604 Apoe apolipoprotein E gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20141003 MGI PMID:16079201 733604 Apoe apolipoprotein E gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11431458 733604 Apoe apolipoprotein E gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12868005 733604 Apoe apolipoprotein E gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:10683374 733604 Apoe apolipoprotein E gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19023427 733604 Apoe apolipoprotein E gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11726538 733604 Apoe apolipoprotein E gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15353487 733604 Apoe apolipoprotein E gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11726538 733604 Apoe apolipoprotein E gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:15653570 733604 Apoe apolipoprotein E gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:21885846 733604 Apoe apolipoprotein E gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:19347044 733604 Apoe apolipoprotein E gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:19684185 733604 Apoe apolipoprotein E gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17138939 733604 Apoe apolipoprotein E gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:16908765 733604 Apoe apolipoprotein E gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20160630 MGI PMID:25278290 733604 Apoe apolipoprotein E gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20230810 MGI PMID:36073366 733604 Apoe apolipoprotein E gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10744782 733604 Apoe apolipoprotein E gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:12746502 733604 Apoe apolipoprotein E gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:10684907 733604 Apoe apolipoprotein E gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21779871 733604 Apoe apolipoprotein E gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15096538 733604 Apoe apolipoprotein E gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:12105373 733604 Apoe apolipoprotein E gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:12105373 733604 Apoe apolipoprotein E gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0006133 calcified artery IAGP N RGD:5509061 20141003 MGI PMID:12730087 733604 Apoe apolipoprotein E gene MP:0006134 artery occlusion IAGP N RGD:5509061 20141003 MGI PMID:15096455 733604 Apoe apolipoprotein E gene MP:0006134 artery occlusion IAGP N RGD:5509061 20141003 MGI PMID:15297377 733604 Apoe apolipoprotein E gene MP:0006134 artery occlusion IAGP N RGD:5509061 20141003 MGI PMID:24082102 733604 Apoe apolipoprotein E gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:10683374 733604 Apoe apolipoprotein E gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16864727 733604 Apoe apolipoprotein E gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:16864727 733604 Apoe apolipoprotein E gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:19139386 733604 Apoe apolipoprotein E gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18725890 733604 Apoe apolipoprotein E gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:9541503 733604 Apoe apolipoprotein E gene MP:0008009 delayed cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:16908765 733604 Apoe apolipoprotein E gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:12454276 733604 Apoe apolipoprotein E gene MP:0008073 abnormal CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11045969 733604 Apoe apolipoprotein E gene MP:0008073 abnormal CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9541503 733604 Apoe apolipoprotein E gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17296788 733604 Apoe apolipoprotein E gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20210617 MGI PMID:19139386 733604 Apoe apolipoprotein E gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:9541503 733604 Apoe apolipoprotein E gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:15708438 733604 Apoe apolipoprotein E gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18325838 733604 Apoe apolipoprotein E gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18325838 733604 Apoe apolipoprotein E gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18325838 733604 Apoe apolipoprotein E gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:18325838 733604 Apoe apolipoprotein E gene MP:0008243 abnormal macrophage derived foam cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10772649 733604 Apoe apolipoprotein E gene MP:0008243 abnormal macrophage derived foam cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23383297 733604 Apoe apolipoprotein E gene MP:0008248 abnormal mononuclear phagocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17138939 733604 Apoe apolipoprotein E gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10684907 733604 Apoe apolipoprotein E gene MP:0008289 abnormal adrenal medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:10684907 733604 Apoe apolipoprotein E gene MP:0008389 hypochromic macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:11861300 733604 Apoe apolipoprotein E gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20160630 MGI PMID:25278290 733604 Apoe apolipoprotein E gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:15794991 733604 Apoe apolipoprotein E gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:15794991 733604 Apoe apolipoprotein E gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:11431458 733604 Apoe apolipoprotein E gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:11431458 733604 Apoe apolipoprotein E gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:16079201 733604 Apoe apolipoprotein E gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:15033273 733604 Apoe apolipoprotein E gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20161020 MGI PMID:19858416 733604 Apoe apolipoprotein E gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20240523 MGI PMID:32686880 733604 Apoe apolipoprotein E gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:14507923 733604 Apoe apolipoprotein E gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:14507923 733604 Apoe apolipoprotein E gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23383297 733604 Apoe apolipoprotein E gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17138939 733604 Apoe apolipoprotein E gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17138939 733604 Apoe apolipoprotein E gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9541503 733604 Apoe apolipoprotein E gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:12765335 733604 Apoe apolipoprotein E gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20240523 MGI PMID:32686880 733604 Apoe apolipoprotein E gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:19347044 733604 Apoe apolipoprotein E gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:12765335 733604 Apoe apolipoprotein E gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:17138939 733604 Apoe apolipoprotein E gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:14507923 733604 Apoe apolipoprotein E gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:14507923 733604 Apoe apolipoprotein E gene MP:0008817 hematoma IAGP N RGD:5509061 20141003 MGI PMID:19139386 733604 Apoe apolipoprotein E gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:16079201 733604 Apoe apolipoprotein E gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10514484 733604 Apoe apolipoprotein E gene MP:0009115 abnormal fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18725890 733604 Apoe apolipoprotein E gene MP:0009122 decreased white fat cell lipid droplet size IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23383297 733604 Apoe apolipoprotein E gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20160414 MGI PMID:10684907 733604 Apoe apolipoprotein E gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:9326295 733604 Apoe apolipoprotein E gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12746502 733604 Apoe apolipoprotein E gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15096455 733604 Apoe apolipoprotein E gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19139386 733604 Apoe apolipoprotein E gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23999430 733604 Apoe apolipoprotein E gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16908765 733604 Apoe apolipoprotein E gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:17242161 733604 Apoe apolipoprotein E gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15653570 733604 Apoe apolipoprotein E gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15914123 733604 Apoe apolipoprotein E gene MP:0009864 abnormal aorta endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19048083 733604 Apoe apolipoprotein E gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:19048083 733604 Apoe apolipoprotein E gene MP:0009868 abnormal descending thoracic aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16864727 733604 Apoe apolipoprotein E gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:15653570 733604 Apoe apolipoprotein E gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141003 MGI PMID:10727439 733604 Apoe apolipoprotein E gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20160204 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0010161 decreased brain cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10655544 733604 Apoe apolipoprotein E gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:12765335 733604 Apoe apolipoprotein E gene MP:0010331 abnormal apolipoprotein level IAGP N RGD:5509061 20141003 MGI PMID:22441102 733604 Apoe apolipoprotein E gene MP:0010331 abnormal apolipoprotein level IAGP N RGD:5509061 20141003 MGI PMID:9169506 733604 Apoe apolipoprotein E gene MP:0010333 abnormal circulating apolipoprotein E level IAGP N RGD:5509061 20201002 MGI PMID:10938015 733604 Apoe apolipoprotein E gene MP:0010451 kidney microaneurysm IAGP N RGD:5509061 20141003 MGI PMID:12177238 733604 Apoe apolipoprotein E gene MP:0010483 aortic sinus aneurysm IAGP N RGD:5509061 20141003 MGI PMID:10683374 733604 Apoe apolipoprotein E gene MP:0010574 dilated aorta IAGP N RGD:5509061 20141003 MGI PMID:19139386 733604 Apoe apolipoprotein E gene MP:0010658 thoracic aorta aneurysm IAGP N RGD:5509061 20141003 MGI PMID:19139386 733604 Apoe apolipoprotein E gene MP:0010663 abnormal brachiocephalic trunk morphology IAGP N RGD:5509061 20141003 MGI PMID:16840715 733604 Apoe apolipoprotein E gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:11468208 733604 Apoe apolipoprotein E gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15914123 733604 Apoe apolipoprotein E gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17068284 733604 Apoe apolipoprotein E gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20201002 MGI PMID:31102955 733604 Apoe apolipoprotein E gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:15647822 733604 Apoe apolipoprotein E gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0010875 increased bone volume IAGP N RGD:5509061 20220922 MGI PMID:15647822 733604 Apoe apolipoprotein E gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20220922 MGI PMID:15647822 733604 Apoe apolipoprotein E gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:18344414 733604 Apoe apolipoprotein E gene MP:0010922 alveolitis IAGP N RGD:5509061 20141003 MGI PMID:20026782 733604 Apoe apolipoprotein E gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0010935 increased airway resistance IAGP N RGD:5509061 20141003 MGI PMID:18344414 733604 Apoe apolipoprotein E gene MP:0010950 abnormal lung hysteresivity IAGP N RGD:5509061 20141003 MGI PMID:18344414 733604 Apoe apolipoprotein E gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18988889 733604 Apoe apolipoprotein E gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12746502 733604 Apoe apolipoprotein E gene MP:0011231 abnormal vitamin E level IAGP N RGD:5509061 20141003 MGI PMID:11095717 733604 Apoe apolipoprotein E gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0011309 abnormal kidney arterial blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12177238 733604 Apoe apolipoprotein E gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:21779871 733604 Apoe apolipoprotein E gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:12177238 733604 Apoe apolipoprotein E gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:12177238 733604 Apoe apolipoprotein E gene MP:0011477 abnormal urine nucleoside level IAGP N RGD:5509061 20141003 MGI PMID:17549254 733604 Apoe apolipoprotein E gene MP:0011508 abnormal glomerular capillary thrombosis IAGP N RGD:5509061 20141003 MGI PMID:12177238 733604 Apoe apolipoprotein E gene MP:0011509 dilated glomerular capillary IAGP N RGD:5509061 20141003 MGI PMID:12177238 733604 Apoe apolipoprotein E gene MP:0011561 renal glomerulus lipidosis IAGP N RGD:5509061 20141003 MGI PMID:12177238 733604 Apoe apolipoprotein E gene MP:0011567 increased renal glomerulus lobularity IAGP N RGD:5509061 20141003 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0011572 abnormal aorta bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0011578 increased lipoprotein lipase activity IAGP N RGD:5509061 20141003 MGI PMID:12454276 733604 Apoe apolipoprotein E gene MP:0011581 increased triglyceride lipase activity IAGP N RGD:5509061 20141003 MGI PMID:12454276 733604 Apoe apolipoprotein E gene MP:0011599 increased phosphatidylcholine-sterol O-acyltransferase activity IAGP N RGD:5509061 20141003 MGI PMID:12538880 733604 Apoe apolipoprotein E gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:10684907 733604 Apoe apolipoprotein E gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:10684907 733604 Apoe apolipoprotein E gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:11045969 733604 Apoe apolipoprotein E gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:16051453 733604 Apoe apolipoprotein E gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20151231 MGI PMID:18550766 733604 Apoe apolipoprotein E gene MP:0012329 increased circulating factor VIII level IAGP N RGD:5509061 20201002 MGI PMID:14739216 733604 Apoe apolipoprotein E gene MP:0012329 increased circulating factor VIII level IAGP N RGD:5509061 20201002 MGI PMID:15840700 733604 Apoe apolipoprotein E gene MP:0012334 decreased circulating homocysteine level IAGP N RGD:5509061 20180920 MGI PMID:11726538 733604 Apoe apolipoprotein E gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20161020 MGI PMID:19858416 733604 Apoe apolipoprotein E gene MP:0013022 increased Ly6C high monocyte number IAGP N RGD:5509061 20161020 MGI PMID:19858416 733604 Apoe apolipoprotein E gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:10684907 733604 Apoe apolipoprotein E gene MP:0014370 impaired spatial working memory IAGP N RGD:5509061 20240328 MGI PMID:11476599 733604 Apoe apolipoprotein E gene MP:0014431 increased chemokine level IAGP N RGD:5509061 20240523 MGI PMID:32686880 733604 Apoe apolipoprotein E gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0020100 decreased susceptibility to diet-induced aortic fatty streak lesions IEA N RGD:5509061 20220811 MGI 733604 Apoe apolipoprotein E gene MP:0020253 increased collagen level IAGP N RGD:5509061 20151231 MGI PMID:22939356 733604 Apoe apolipoprotein E gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0021025 increased cerebrospinal fluid amyloid beta 40 isoform level IAGP N RGD:5509061 20220310 MGI PMID:14741101 733604 Apoe apolipoprotein E gene MP:0021027 abnormal cerebrospinal fluid amyloid beta 40 isoform level IAGP N RGD:5509061 20220310 MGI PMID:15772340 733604 Apoe apolipoprotein E gene MP:0021082 abnormal cerebrospinal fluid amyloid beta 42 isoform level IAGP N RGD:5509061 20220310 MGI PMID:15772340 733604 Apoe apolipoprotein E gene MP:0021083 increased cerebrospinal fluid amyloid beta 42 isoform level IAGP N RGD:5509061 20220310 MGI PMID:14741101 733604 Apoe apolipoprotein E gene MP:0021161 increased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:11468208 733604 Apoe apolipoprotein E gene MP:0021186 decreased bone mineral density of vertebrae IAGP N RGD:5509061 20220915 MGI PMID:17259598 733604 Apoe apolipoprotein E gene MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20220922 MGI PMID:15647822 733604 Apoe apolipoprotein E gene MP:0030644 increased circulating methionine level IAGP N RGD:5509061 20180920 MGI PMID:19858416 733604 Apoe apolipoprotein E gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:21779871 733604 Apoe apolipoprotein E gene MP:0031059 increased circulating C-reactive protein level IAGP N RGD:5509061 20201002 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0031076 decreased circulating troponin level IAGP N RGD:5509061 20200618 MGI PMID:15031124 733604 Apoe apolipoprotein E gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:19481534 733604 Apoe apolipoprotein E gene MP:0031157 abnormal arterial thrombosis IAGP N RGD:5509061 20201210 MGI PMID:12765335 733604 Apoe apolipoprotein E gene MP:0031165 increased circulating von Willebrand factor level IAGP N RGD:5509061 20201015 MGI PMID:14739216 733604 Apoe apolipoprotein E gene MP:0031233 decreased circulating serum amyloid protein level IAGP N RGD:5509061 20210225 MGI PMID:15914123 733604 Apoe apolipoprotein E gene MP:0031271 increased susceptibility to age-related hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:22185842 733604 Apoe apolipoprotein E gene MP:0031273 decreased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:14597759 733604 Apoe apolipoprotein E gene MP:0031274 increased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:11468208 733604 Apoe apolipoprotein E gene MP:0031274 increased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:19139386 733604 Apoe apolipoprotein E gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:11312553 733604 Apoe apolipoprotein E gene MP:0031414 decreased skeletal muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0031417 decreased cardiac muscle triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:25421060 733604 Apoe apolipoprotein E gene MP:0031510 increased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:16908765 733607 Ccs copper chaperone for superoxide dismutase gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10694572 733607 Ccs copper chaperone for superoxide dismutase gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10694572 733607 Ccs copper chaperone for superoxide dismutase gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10694572 733607 Ccs copper chaperone for superoxide dismutase gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:10694572 733607 Ccs copper chaperone for superoxide dismutase gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:10694572 733607 Ccs copper chaperone for superoxide dismutase gene MP:0003951 abnormal copper homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10694572 733607 Ccs copper chaperone for superoxide dismutase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:10694572 733607 Ccs copper chaperone for superoxide dismutase gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:10694572 733609 H3f3b H3.3 histone B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23315948 733609 H3f3b H3.3 histone B gene MP:0001488 increased startle reflex IEA N RGD:5509061 20231207 MGI 733609 H3f3b H3.3 histone B gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:23570311 733609 H3f3b H3.3 histone B gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23315948 733609 H3f3b H3.3 histone B gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:23570311 733609 H3f3b H3.3 histone B gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210805 MGI 733609 H3f3b H3.3 histone B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23315948 733609 H3f3b H3.3 histone B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23570311 733609 H3f3b H3.3 histone B gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:23570311 733609 H3f3b H3.3 histone B gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:23570311 733609 H3f3b H3.3 histone B gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:23570311 733609 H3f3b H3.3 histone B gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23570311 733609 H3f3b H3.3 histone B gene MP:0004025 polyploidy IAGP N RGD:5509061 20141003 MGI PMID:23570311 733609 H3f3b H3.3 histone B gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210805 MGI 733609 H3f3b H3.3 histone B gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:23315948 733609 H3f3b H3.3 histone B gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210805 MGI 733609 H3f3b H3.3 histone B gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23570311 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:11336498 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11336498 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11336498 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210520 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:11336498 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210520 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0001406 abnormal gait IEA N RGD:5509061 20210520 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20210520 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210826 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0001512 trunk curl IEA N RGD:5509061 20210520 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:11336498 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11336498 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11336498 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11336498 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210520 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11336498 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11336498 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20210520 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11336498 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210520 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20221215 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210826 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0010379 decreased respiratory quotient IEA N RGD:5509061 20210520 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11336498 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11336498 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0011940 decreased food intake IEA N RGD:5509061 20210520 MGI 733610 Strbp spermatid perinuclear RNA binding protein gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210520 MGI 733612 Nup88 nucleoporin 88 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20191205 MGI PMID:26731471 733614 Gsta3 glutathione S-transferase, alpha 3 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19850059 733614 Gsta3 glutathione S-transferase, alpha 3 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19850059 733619 Dnm1l dynamin 1-like gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20210826 MGI 733619 Dnm1l dynamin 1-like gene MP:0000597 delayed hepatic development IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20160421 MGI 733619 Dnm1l dynamin 1-like gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201231 MGI 733619 Dnm1l dynamin 1-like gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0001714 absent trophoblast giant cells IAGP N RGD:5509061 20141003 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20201231 MGI 733619 Dnm1l dynamin 1-like gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0003889 enhanced sensorimotor gating IAGP N RGD:5509061 20200820 MGI PMID:31603426 733619 Dnm1l dynamin 1-like gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0005426 tachypnea IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20201231 MGI 733619 Dnm1l dynamin 1-like gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20200820 MGI PMID:31603426 733619 Dnm1l dynamin 1-like gene MP:0008775 abnormal heart ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0009027 abnormal subarachnoid space morphology IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20200820 MGI PMID:31603426 733619 Dnm1l dynamin 1-like gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20200820 MGI PMID:31603426 733619 Dnm1l dynamin 1-like gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20200820 MGI PMID:31603426 733619 Dnm1l dynamin 1-like gene MP:0010017 visceral vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0010334 pleural effusion IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733619 Dnm1l dynamin 1-like gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0011630 increased mitochondrial size IAGP N RGD:5509061 20160428 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0011705 absent fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0014010 abnormal peroxisome morphology IAGP N RGD:5509061 20160428 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0014010 abnormal peroxisome morphology IAGP N RGD:5509061 20230615 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0014178 increased brain apoptosis IAGP N RGD:5509061 20160428 MGI PMID:19578372 733619 Dnm1l dynamin 1-like gene MP:0014331 abnormal Purkinje cell mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:19752021 733619 Dnm1l dynamin 1-like gene MP:0014343 abnormal myocardial fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:20585624 733619 Dnm1l dynamin 1-like gene MP:0030309 abnormal posterior cranial fossa morphology IAGP N RGD:5509061 20171109 MGI PMID:19578372 733621 Gtf2a1 general transcription factor II A, 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:24176642 733621 Gtf2a1 general transcription factor II A, 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:24176642 733621 Gtf2a1 general transcription factor II A, 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:24176642 733621 Gtf2a1 general transcription factor II A, 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:24176642 733621 Gtf2a1 general transcription factor II A, 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:24176642 733621 Gtf2a1 general transcription factor II A, 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:24176642 733621 Gtf2a1 general transcription factor II A, 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:24176642 733621 Gtf2a1 general transcription factor II A, 1 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:24176642 733621 Gtf2a1 general transcription factor II A, 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 733621 Gtf2a1 general transcription factor II A, 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24176642 733621 Gtf2a1 general transcription factor II A, 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733621 Gtf2a1 general transcription factor II A, 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:24176642 733622 Cst6 cystatin E/M gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20230601 MGI 733622 Cst6 cystatin E/M gene MP:0000154 rib fusion IEA N RGD:5509061 20230601 MGI 733622 Cst6 cystatin E/M gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 733622 Cst6 cystatin E/M gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 733622 Cst6 cystatin E/M gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9212754 733622 Cst6 cystatin E/M gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:9212754 733622 Cst6 cystatin E/M gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9212754 733622 Cst6 cystatin E/M gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 733622 Cst6 cystatin E/M gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 733622 Cst6 cystatin E/M gene MP:0000692 small spleen IEA N RGD:5509061 20230601 MGI 733622 Cst6 cystatin E/M gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 733622 Cst6 cystatin E/M gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:9212754 733622 Cst6 cystatin E/M gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:9212754 733622 Cst6 cystatin E/M gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:9212754 733622 Cst6 cystatin E/M gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:9212754 733622 Cst6 cystatin E/M gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9212754 733622 Cst6 cystatin E/M gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:9212754 733622 Cst6 cystatin E/M gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:9212754 733622 Cst6 cystatin E/M gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15044380 733622 Cst6 cystatin E/M gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9212754 733622 Cst6 cystatin E/M gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 733622 Cst6 cystatin E/M gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:9212754 733622 Cst6 cystatin E/M gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20231207 MGI 733622 Cst6 cystatin E/M gene MP:0004357 long tibia IEA N RGD:5509061 20240523 MGI 733622 Cst6 cystatin E/M gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 733622 Cst6 cystatin E/M gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:9212754 733622 Cst6 cystatin E/M gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:9212754 733622 Cst6 cystatin E/M gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20141003 MGI PMID:12393798 733622 Cst6 cystatin E/M gene MP:0009709 hydrometra IEA N RGD:5509061 20230601 MGI 733622 Cst6 cystatin E/M gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20230601 MGI 733622 Cst6 cystatin E/M gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12393798 733622 Cst6 cystatin E/M gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15044380 733622 Cst6 cystatin E/M gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9212754 733622 Cst6 cystatin E/M gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 733622 Cst6 cystatin E/M gene MP:0012725 small sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:9212754 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:17043146 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17043146 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:24163073 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:17043146 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210128 MGI 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17043146 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17043146 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:8798642 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17043146 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:17043146 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:17043146 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:17043146 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:17043146 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0002606 increased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17043146 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20151022 MGI PMID:25071151 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20151022 MGI PMID:25071151 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20151022 MGI PMID:25071151 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20151022 MGI PMID:25071151 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17043146 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20151022 MGI PMID:25071151 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20151022 MGI PMID:25071151 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11581143 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:17043146 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20151022 MGI PMID:25071151 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:17043146 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20151022 MGI PMID:25071151 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0009709 hydrometra IEA N RGD:5509061 20181227 MGI 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:17043146 733626 Alox15 arachidonate 15-lipoxygenase gene MP:0020088 decreased susceptibility to non-insulin-dependent diabetes IAGP N RGD:5509061 20151022 MGI PMID:25071151 733630 Plrg1 pleiotropic regulator 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19307306 733630 Plrg1 pleiotropic regulator 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19307306 733630 Plrg1 pleiotropic regulator 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19307306 733630 Plrg1 pleiotropic regulator 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:19307306 733630 Plrg1 pleiotropic regulator 1 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:19307306 733630 Plrg1 pleiotropic regulator 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:19307306 733630 Plrg1 pleiotropic regulator 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:19307306 733630 Plrg1 pleiotropic regulator 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19307306 733630 Plrg1 pleiotropic regulator 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19307306 733630 Plrg1 pleiotropic regulator 1 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:19307306 733630 Plrg1 pleiotropic regulator 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19307306 733630 Plrg1 pleiotropic regulator 1 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19307306 733630 Plrg1 pleiotropic regulator 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19307306 733630 Plrg1 pleiotropic regulator 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19307306 733631 Plekhb1 pleckstrin homology domain containing, family B (evectins) member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15456885 733633 Gabrg3 gamma-aminobutyric acid type A receptor, subunit gamma 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20190502 MGI 733633 Gabrg3 gamma-aminobutyric acid type A receptor, subunit gamma 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 733633 Gabrg3 gamma-aminobutyric acid type A receptor, subunit gamma 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20190502 MGI 733634 Cygb cytoglobin gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210805 MGI 733634 Cygb cytoglobin gene MP:0000274 enlarged heart IEA N RGD:5509061 20210805 MGI 733634 Cygb cytoglobin gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24367119 733634 Cygb cytoglobin gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:21684245 733634 Cygb cytoglobin gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210805 MGI 733634 Cygb cytoglobin gene MP:0001147 small testis IEA N RGD:5509061 20210805 MGI 733634 Cygb cytoglobin gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210805 MGI 733634 Cygb cytoglobin gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 733634 Cygb cytoglobin gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:24367119 733634 Cygb cytoglobin gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21684245 733634 Cygb cytoglobin gene MP:0003960 increased lean body mass IEA N RGD:5509061 20230720 MGI 733634 Cygb cytoglobin gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:21684245 733634 Cygb cytoglobin gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20231207 MGI 733634 Cygb cytoglobin gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24367119 733634 Cygb cytoglobin gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21684245 733634 Cygb cytoglobin gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:24367119 733634 Cygb cytoglobin gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230720 MGI 733634 Cygb cytoglobin gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230720 MGI 733634 Cygb cytoglobin gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20141003 MGI PMID:21684245 733634 Cygb cytoglobin gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:24367119 733634 Cygb cytoglobin gene MP:0012186 abnormal muscle precursor cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24367119 733634 Cygb cytoglobin gene MP:0013160 impaired muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:24367119 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23064362 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23064362 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20231207 MGI 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:17908936 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17908936 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:23064362 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20201029 MGI PMID:28176791 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:23064362 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20201029 MGI PMID:28327619 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23064362 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20201029 MGI PMID:28327619 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:23064362 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0008712 decreased interleukin-9 secretion IAGP N RGD:5509061 20201029 MGI PMID:28327619 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:23064362 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20201029 MGI PMID:28176791 733637 Il1rl2 interleukin 1 receptor-like 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 733639 Gata3 GATA binding protein 3 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11135239 733639 Gata3 GATA binding protein 3 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:11135239 733639 Gata3 GATA binding protein 3 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:15207274 733639 Gata3 GATA binding protein 3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10439272 733639 Gata3 GATA binding protein 3 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:10439272 733639 Gata3 GATA binding protein 3 gene MP:0000414 alopecia IEA N RGD:5509061 20141003 MGI 733639 Gata3 GATA binding protein 3 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:10439272 733639 Gata3 GATA binding protein 3 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:14670303 733639 Gata3 GATA binding protein 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:14670303 733639 Gata3 GATA binding protein 3 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19934022 733639 Gata3 GATA binding protein 3 gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8945476 733639 Gata3 GATA binding protein 3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:11135239 733639 Gata3 GATA binding protein 3 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20702712 733639 Gata3 GATA binding protein 3 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:20702712 733639 Gata3 GATA binding protein 3 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0001274 curly vibrissae IEA N RGD:5509061 20141003 MGI 733639 Gata3 GATA binding protein 3 gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:20702712 733639 Gata3 GATA binding protein 3 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:10835639 733639 Gata3 GATA binding protein 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20702712 733639 Gata3 GATA binding protein 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17658279 733639 Gata3 GATA binding protein 3 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14670303 733639 Gata3 GATA binding protein 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20141003 MGI PMID:10439272 733639 Gata3 GATA binding protein 3 gene MP:0002074 abnormal hair texture IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:7550312 733639 Gata3 GATA binding protein 3 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19934022 733639 Gata3 GATA binding protein 3 gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:7550312 733639 Gata3 GATA binding protein 3 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:10439272 733639 Gata3 GATA binding protein 3 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7550312 733639 Gata3 GATA binding protein 3 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7550312 733639 Gata3 GATA binding protein 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14670303 733639 Gata3 GATA binding protein 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18776904 733639 Gata3 GATA binding protein 3 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19934022 733639 Gata3 GATA binding protein 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:7550312 733639 Gata3 GATA binding protein 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:7550312 733639 Gata3 GATA binding protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15475959 733639 Gata3 GATA binding protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7550312 733639 Gata3 GATA binding protein 3 gene MP:0002234 abnormal pharynx morphology IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19934022 733639 Gata3 GATA binding protein 3 gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15475959 733639 Gata3 GATA binding protein 3 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7550312 733639 Gata3 GATA binding protein 3 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:15475959 733639 Gata3 GATA binding protein 3 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:7550312 733639 Gata3 GATA binding protein 3 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0002639 micrognathia IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:10835639 733639 Gata3 GATA binding protein 3 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:24327562 733639 Gata3 GATA binding protein 3 gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:11135239 733639 Gata3 GATA binding protein 3 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:11135239 733639 Gata3 GATA binding protein 3 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11135239 733639 Gata3 GATA binding protein 3 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:10439272 733639 Gata3 GATA binding protein 3 gene MP:0003810 abnormal hair cuticle IAGP N RGD:5509061 20141003 MGI PMID:10439272 733639 Gata3 GATA binding protein 3 gene MP:0003827 abnormal Wolffian duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16319112 733639 Gata3 GATA binding protein 3 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:20702712 733639 Gata3 GATA binding protein 3 gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:14670303 733639 Gata3 GATA binding protein 3 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0004161 cervical aortic arch IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:11135239 733639 Gata3 GATA binding protein 3 gene MP:0004315 absent vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:11135239 733639 Gata3 GATA binding protein 3 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15207274 733639 Gata3 GATA binding protein 3 gene MP:0004369 absent utricle IAGP N RGD:5509061 20141003 MGI PMID:11135239 733639 Gata3 GATA binding protein 3 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15207274 733639 Gata3 GATA binding protein 3 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15994092 733639 Gata3 GATA binding protein 3 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15207274 733639 Gata3 GATA binding protein 3 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15994092 733639 Gata3 GATA binding protein 3 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0004408 decreased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:15207274 733639 Gata3 GATA binding protein 3 gene MP:0004468 small zygomatic bone IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0004497 decreased organ of Corti supporting cell number IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0004540 small maxilla IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0004562 abnormal inner hair cell synaptic ribbon morphology IAGP N RGD:5509061 20141003 MGI PMID:24327562 733639 Gata3 GATA binding protein 3 gene MP:0004586 pillar cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15207274 733639 Gata3 GATA binding protein 3 gene MP:0004592 small mandible IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0004664 delayed inner ear development IAGP N RGD:5509061 20141003 MGI PMID:11135239 733639 Gata3 GATA binding protein 3 gene MP:0004664 delayed inner ear development IAGP N RGD:5509061 20141003 MGI PMID:15499560 733639 Gata3 GATA binding protein 3 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:15994092 733639 Gata3 GATA binding protein 3 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:15207274 733639 Gata3 GATA binding protein 3 gene MP:0004861 abnormal Raphe nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:20818386 733639 Gata3 GATA binding protein 3 gene MP:0004923 absent common crus IAGP N RGD:5509061 20141003 MGI PMID:11135239 733639 Gata3 GATA binding protein 3 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22138715 733639 Gata3 GATA binding protein 3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15475959 733639 Gata3 GATA binding protein 3 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:22138715 733639 Gata3 GATA binding protein 3 gene MP:0005072 abnormal hair follicle melanin granule morphology IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:19934022 733639 Gata3 GATA binding protein 3 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14670303 733639 Gata3 GATA binding protein 3 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:11135239 733639 Gata3 GATA binding protein 3 gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:11135239 733639 Gata3 GATA binding protein 3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:22588720 733639 Gata3 GATA binding protein 3 gene MP:0006286 inner ear hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0006287 inner ear cyst IAGP N RGD:5509061 20141003 MGI PMID:11135239 733639 Gata3 GATA binding protein 3 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:19934022 733639 Gata3 GATA binding protein 3 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14670303 733639 Gata3 GATA binding protein 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14670303 733639 Gata3 GATA binding protein 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18776904 733639 Gata3 GATA binding protein 3 gene MP:0008077 abnormal CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14670303 733639 Gata3 GATA binding protein 3 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14670303 733639 Gata3 GATA binding protein 3 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:15475959 733639 Gata3 GATA binding protein 3 gene MP:0008091 decreased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:15475959 733639 Gata3 GATA binding protein 3 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19934022 733639 Gata3 GATA binding protein 3 gene MP:0008380 abnormal gonial bone morphology IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0008487 abnormal mesonephros morphology IAGP N RGD:5509061 20141003 MGI PMID:16319112 733639 Gata3 GATA binding protein 3 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17658279 733639 Gata3 GATA binding protein 3 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:21460847 733639 Gata3 GATA binding protein 3 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:17658279 733639 Gata3 GATA binding protein 3 gene MP:0008733 abnormal hair shaft melanin granule distribution IAGP N RGD:5509061 20141003 MGI PMID:10439272 733639 Gata3 GATA binding protein 3 gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0009073 absent Wolffian ducts IAGP N RGD:5509061 20141003 MGI PMID:16319112 733639 Gata3 GATA binding protein 3 gene MP:0009284 abnormal sympathetic neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:20702712 733639 Gata3 GATA binding protein 3 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0009733 absent nipple IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0009861 abnormal pyloric sphincter morphology IAGP N RGD:5509061 20161216 MGI PMID:24120474 733639 Gata3 GATA binding protein 3 gene MP:0009880 decreased mouth size IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:20818386 733639 Gata3 GATA binding protein 3 gene MP:0010202 focal dorsal hair loss IAGP N RGD:5509061 20141003 MGI PMID:10439272 733639 Gata3 GATA binding protein 3 gene MP:0010249 lactation failure IAGP N RGD:5509061 20141003 MGI PMID:22588720 733639 Gata3 GATA binding protein 3 gene MP:0010355 abnormal first pharyngeal arch artery morphology IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0010356 abnormal second pharyngeal arch artery morphology IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0010650 abnormal aorticopulmonary septum morphology IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0010684 abnormal hair follicle outer root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0010690 thick hair follicle outer root sheath IAGP N RGD:5509061 20141003 MGI PMID:17151017 733639 Gata3 GATA binding protein 3 gene MP:0010780 abnormal stomach smooth muscle circular layer morphology IAGP N RGD:5509061 20161216 MGI PMID:24120474 733639 Gata3 GATA binding protein 3 gene MP:0010805 abnormal stomach smooth muscle outer longitudinal layer morphology IAGP N RGD:5509061 20161216 MGI PMID:24120474 733639 Gata3 GATA binding protein 3 gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:16319112 733639 Gata3 GATA binding protein 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11135239 733639 Gata3 GATA binding protein 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16319112 733639 Gata3 GATA binding protein 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20231130 MGI PMID:18955134 733639 Gata3 GATA binding protein 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14670303 733639 Gata3 GATA binding protein 3 gene MP:0011238 abnormal inner ear development IAGP N RGD:5509061 20141003 MGI PMID:23666531 733639 Gata3 GATA binding protein 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15207274 733639 Gata3 GATA binding protein 3 gene MP:0013781 abnormal mammary gland luminal epithelium morphology IAGP N RGD:5509061 20150625 MGI PMID:22588720 733639 Gata3 GATA binding protein 3 gene MP:0013818 abnormal oral cavity morphology IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0030080 small lower incisors IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0030086 bony syngnathia IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0030100 hemifacial hypoplasia IAGP N RGD:5509061 20220804 MGI PMID:34383890 733639 Gata3 GATA binding protein 3 gene MP:0030111 absent temporomandibular joint IAGP N RGD:5509061 20220804 MGI PMID:34383890 733643 Cd244a CD244 molecule A gene MP:0003080 increased natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:15356144 733643 Cd244a CD244 molecule A gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:20962259 733643 Cd244a CD244 molecule A gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:23162753 733643 Cd244a CD244 molecule A gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23162753 733645 Hnmt histamine N-methyltransferase gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20180201 MGI PMID:29162912 733645 Hnmt histamine N-methyltransferase gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20180201 MGI PMID:29162912 733645 Hnmt histamine N-methyltransferase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180201 MGI PMID:29162912 733645 Hnmt histamine N-methyltransferase gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20180201 MGI PMID:29162912 733645 Hnmt histamine N-methyltransferase gene MP:0012289 abnormal non-rapid eye movement sleep pattern IAGP N RGD:5509061 20180201 MGI PMID:29162912 733645 Hnmt histamine N-methyltransferase gene MP:0030755 increased histamine level IAGP N RGD:5509061 20180927 MGI PMID:29162912 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0000753 paralysis IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0000852 small cerebellum IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10364163 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:10364163 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0001255 decreased body height IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0001265 decreased body size IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0001388 abnormal stationary movement IEA N RGD:5509061 20150723 MGI 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0001504 abnormal posture IEA N RGD:5509061 20150723 MGI 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0001522 impaired swimming IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0001525 impaired balance IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:10364163 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10364163 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11094085 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19008375 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:19008375 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0002083 premature death IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10364163 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10364163 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:19008375 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:19008375 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0002880 opisthotonus IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0003062 abnormal coping response IEA N RGD:5509061 20160804 MGI 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19008375 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:19008375 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10364163 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11094085 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:10364163 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0004557 dilated allantois IAGP N RGD:5509061 20141003 MGI PMID:10364163 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0004706 short vertebral body IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0005150 cachexia IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0005156 bradykinesia IEA N RGD:5509061 20150723 MGI 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10364163 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0005424 jerky movement IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15640163 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0006205 embryonic lethality between implantation and somite formation IEA N RGD:5509061 20141003 MGI 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19008375 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0008503 abnormal spinal cord grey matter morphology IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0009393 abnormal resting posture IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:10364163 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19008375 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11094085 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10364163 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15640163 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220519 MGI 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0012083 absent foregut IAGP N RGD:5509061 20141003 MGI PMID:10364163 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0012263 decreased hindbrain size IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0012484 decreased corticospinal tract size IAGP N RGD:5509061 20150723 MGI PMID:6024256 733650 Hgs HGF-regulated tyrosine kinase substrate gene MP:0020533 decreased pons size IAGP N RGD:5509061 20180301 MGI PMID:6024256 733653 Ica1 islet cell autoantigen 1 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20181227 MGI 733653 Ica1 islet cell autoantigen 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 733653 Ica1 islet cell autoantigen 1 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 733653 Ica1 islet cell autoantigen 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 733653 Ica1 islet cell autoantigen 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20161117 MGI PMID:26306493 733653 Ica1 islet cell autoantigen 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20161117 MGI PMID:26306493 733653 Ica1 islet cell autoantigen 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11751995 733653 Ica1 islet cell autoantigen 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11751995 733653 Ica1 islet cell autoantigen 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 733653 Ica1 islet cell autoantigen 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 733653 Ica1 islet cell autoantigen 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11751995 733653 Ica1 islet cell autoantigen 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11751995 733653 Ica1 islet cell autoantigen 1 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20161117 MGI PMID:26306493 733653 Ica1 islet cell autoantigen 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20161117 MGI PMID:26306493 733653 Ica1 islet cell autoantigen 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 733653 Ica1 islet cell autoantigen 1 gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:11751995 733653 Ica1 islet cell autoantigen 1 gene MP:0008839 absent acrosome IAGP N RGD:5509061 20161117 MGI PMID:26306493 733653 Ica1 islet cell autoantigen 1 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20161117 MGI PMID:26306493 733653 Ica1 islet cell autoantigen 1 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20161117 MGI PMID:26306493 733653 Ica1 islet cell autoantigen 1 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20181227 MGI 733653 Ica1 islet cell autoantigen 1 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20161117 MGI PMID:26306493 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20200827 MGI PMID:25122198 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0001469 abnormal contextual conditioning behavior IEA N RGD:5509061 20210128 MGI 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20160204 MGI PMID:24600012 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23512661 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16428450 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200423 MGI PMID:30626688 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0003608 prostate gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:23512661 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20200827 MGI PMID:25122198 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0005140 decreased cardiac muscle contractility IEA N RGD:5509061 20211021 MGI 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:23512661 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23512661 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0009737 prostate gland cyst IAGP N RGD:5509061 20141003 MGI PMID:23512661 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20141003 MGI PMID:23512661 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20190502 MGI 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0020947 decreased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200528 MGI PMID:31099738 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0020947 decreased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200827 MGI PMID:24348248 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:30626688 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0031045 decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:24600012 733656 Tmprss2 transmembrane protease, serine 2 gene MP:0031045 decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200528 MGI PMID:31099738 733657 Lta lymphotoxin A gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8171322 733657 Lta lymphotoxin A gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7636227 733657 Lta lymphotoxin A gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8171322 733657 Lta lymphotoxin A gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8671586 733657 Lta lymphotoxin A gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9368616 733657 Lta lymphotoxin A gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20160211 MGI 733657 Lta lymphotoxin A gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20160211 MGI 733657 Lta lymphotoxin A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 733657 Lta lymphotoxin A gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 733657 Lta lymphotoxin A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:16406654 733657 Lta lymphotoxin A gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:16705172 733657 Lta lymphotoxin A gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11733579 733657 Lta lymphotoxin A gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:8171322 733657 Lta lymphotoxin A gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:8671586 733657 Lta lymphotoxin A gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9133428 733657 Lta lymphotoxin A gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9368616 733657 Lta lymphotoxin A gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9565643 733657 Lta lymphotoxin A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16705172 733657 Lta lymphotoxin A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9368616 733657 Lta lymphotoxin A gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:16406654 733657 Lta lymphotoxin A gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16406654 733657 Lta lymphotoxin A gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:21436282 733657 Lta lymphotoxin A gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12163535 733657 Lta lymphotoxin A gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:9834074 733657 Lta lymphotoxin A gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:16705172 733657 Lta lymphotoxin A gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:7636227 733657 Lta lymphotoxin A gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:8671586 733657 Lta lymphotoxin A gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:9133428 733657 Lta lymphotoxin A gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:7636227 733657 Lta lymphotoxin A gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:8671586 733657 Lta lymphotoxin A gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18384745 733657 Lta lymphotoxin A gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18384745 733657 Lta lymphotoxin A gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:8171322 733657 Lta lymphotoxin A gene MP:0002345 abnormal lymph node primary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16705172 733657 Lta lymphotoxin A gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:12115620 733657 Lta lymphotoxin A gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:9368616 733657 Lta lymphotoxin A gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:8171322 733657 Lta lymphotoxin A gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:8671586 733657 Lta lymphotoxin A gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:21441458 733657 Lta lymphotoxin A gene MP:0002377 abnormal mucosa-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15632007 733657 Lta lymphotoxin A gene MP:0002378 abnormal gut-associated lymphoid tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15247480 733657 Lta lymphotoxin A gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16705172 733657 Lta lymphotoxin A gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9130661 733657 Lta lymphotoxin A gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9834074 733657 Lta lymphotoxin A gene MP:0002450 abnormal lymph organ development IAGP N RGD:5509061 20141003 MGI PMID:11733579 733657 Lta lymphotoxin A gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9368616 733657 Lta lymphotoxin A gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:7636227 733657 Lta lymphotoxin A gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9834074 733657 Lta lymphotoxin A gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21441458 733657 Lta lymphotoxin A gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:16406654 733657 Lta lymphotoxin A gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:18384745 733657 Lta lymphotoxin A gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:9565643 733657 Lta lymphotoxin A gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:16705172 733657 Lta lymphotoxin A gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:18384745 733657 Lta lymphotoxin A gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:7636227 733657 Lta lymphotoxin A gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:8171322 733657 Lta lymphotoxin A gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:8671586 733657 Lta lymphotoxin A gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:9368616 733657 Lta lymphotoxin A gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:9565643 733657 Lta lymphotoxin A gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:16406654 733657 Lta lymphotoxin A gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16406654 733657 Lta lymphotoxin A gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15632007 733657 Lta lymphotoxin A gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:9834074 733657 Lta lymphotoxin A gene MP:0004357 long tibia IAGP N RGD:5509061 20141003 MGI PMID:16406654 733657 Lta lymphotoxin A gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:10064079 733657 Lta lymphotoxin A gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:9565643 733657 Lta lymphotoxin A gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:16705172 733657 Lta lymphotoxin A gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16406654 733657 Lta lymphotoxin A gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:7636227 733657 Lta lymphotoxin A gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 733657 Lta lymphotoxin A gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9565643 733657 Lta lymphotoxin A gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8171322 733657 Lta lymphotoxin A gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8671586 733657 Lta lymphotoxin A gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8171322 733657 Lta lymphotoxin A gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8671586 733657 Lta lymphotoxin A gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:17456769 733657 Lta lymphotoxin A gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9006341 733657 Lta lymphotoxin A gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:8671586 733657 Lta lymphotoxin A gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:10698075 733657 Lta lymphotoxin A gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:10843380 733657 Lta lymphotoxin A gene MP:0005575 increased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 733657 Lta lymphotoxin A gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:16406654 733657 Lta lymphotoxin A gene MP:0006087 increased body mass index IAGP N RGD:5509061 20141003 MGI PMID:16406654 733657 Lta lymphotoxin A gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18384745 733657 Lta lymphotoxin A gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7636227 733657 Lta lymphotoxin A gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8671586 733657 Lta lymphotoxin A gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9368616 733657 Lta lymphotoxin A gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:18384745 733657 Lta lymphotoxin A gene MP:0008169 increased B-1b cell number IAGP N RGD:5509061 20141003 MGI PMID:18384745 733657 Lta lymphotoxin A gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:18384745 733657 Lta lymphotoxin A gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18384745 733657 Lta lymphotoxin A gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:18384745 733657 Lta lymphotoxin A gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:7636227 733657 Lta lymphotoxin A gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:8171322 733657 Lta lymphotoxin A gene MP:0008343 abnormal gamma-delta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21419662 733657 Lta lymphotoxin A gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21436282 733657 Lta lymphotoxin A gene MP:0008464 absent peripheral lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9565643 733657 Lta lymphotoxin A gene MP:0008465 absent mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0008465 absent mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18384745 733657 Lta lymphotoxin A gene MP:0008465 absent mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8171322 733657 Lta lymphotoxin A gene MP:0008465 absent mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9133428 733657 Lta lymphotoxin A gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:18384745 733657 Lta lymphotoxin A gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:16705172 733657 Lta lymphotoxin A gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:7636227 733657 Lta lymphotoxin A gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9834074 733657 Lta lymphotoxin A gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9834074 733657 Lta lymphotoxin A gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9834074 733657 Lta lymphotoxin A gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21436282 733657 Lta lymphotoxin A gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:21436282 733657 Lta lymphotoxin A gene MP:0008552 abnormal circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16705172 733657 Lta lymphotoxin A gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16705172 733657 Lta lymphotoxin A gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:9130661 733657 Lta lymphotoxin A gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16705172 733657 Lta lymphotoxin A gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:9834074 733657 Lta lymphotoxin A gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:9834074 733657 Lta lymphotoxin A gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:9130661 733657 Lta lymphotoxin A gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17502664 733657 Lta lymphotoxin A gene MP:0009544 abnormal thymus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21441458 733657 Lta lymphotoxin A gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0009622 absent inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8171322 733657 Lta lymphotoxin A gene MP:0009628 absent brachial lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8171322 733657 Lta lymphotoxin A gene MP:0009633 absent cervical lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8171322 733657 Lta lymphotoxin A gene MP:0009634 absent popliteal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0009634 absent popliteal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8171322 733657 Lta lymphotoxin A gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10698075 733657 Lta lymphotoxin A gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16705172 733657 Lta lymphotoxin A gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:8671586 733657 Lta lymphotoxin A gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:8671586 733657 Lta lymphotoxin A gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16705172 733657 Lta lymphotoxin A gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9834074 733657 Lta lymphotoxin A gene MP:0012124 increased bronchoconstrictive response IEA N RGD:5509061 20201022 MGI 733657 Lta lymphotoxin A gene MP:0013588 small thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:21441458 733657 Lta lymphotoxin A gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:12446781 733657 Lta lymphotoxin A gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:8671586 733657 Lta lymphotoxin A gene MP:0020928 increased susceptibility to Poxviridae infection IAGP N RGD:5509061 20200430 MGI PMID:8671586 733662 Gfra4 glial cell line derived neurotrophic factor family receptor alpha 4 gene MP:0002876 abnormal thyroid gland physiology IAGP N RGD:5509061 20141003 MGI PMID:16497798 733662 Gfra4 glial cell line derived neurotrophic factor family receptor alpha 4 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:16497798 733662 Gfra4 glial cell line derived neurotrophic factor family receptor alpha 4 gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:16497798 733666 Eln elastin gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:14597767 733666 Eln elastin gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:14597767 733666 Eln elastin gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:15710889 733666 Eln elastin gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:9819363 733666 Eln elastin gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9607766 733666 Eln elastin gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:10970822 733666 Eln elastin gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:10970822 733666 Eln elastin gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:10970822 733666 Eln elastin gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:14597767 733666 Eln elastin gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:22265892 733666 Eln elastin gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:14597767 733666 Eln elastin gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:10970822 733666 Eln elastin gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14597767 733666 Eln elastin gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9607766 733666 Eln elastin gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:22265892 733666 Eln elastin gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:14597767 733666 Eln elastin gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:14597767 733666 Eln elastin gene MP:0003395 abnormal subclavian artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9607766 733666 Eln elastin gene MP:0003410 abnormal artery development IAGP N RGD:5509061 20141003 MGI PMID:9607766 733666 Eln elastin gene MP:0003907 decreased aorta elastin content IAGP N RGD:5509061 20141003 MGI PMID:14597767 733666 Eln elastin gene MP:0003907 decreased aorta elastin content IAGP N RGD:5509061 20141003 MGI PMID:9819363 733666 Eln elastin gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:14597767 733666 Eln elastin gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:15710889 733666 Eln elastin gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9607766 733666 Eln elastin gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9819363 733666 Eln elastin gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:10970822 733666 Eln elastin gene MP:0006083 abnormal blood vessel elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15710889 733666 Eln elastin gene MP:0006083 abnormal blood vessel elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9819363 733666 Eln elastin gene MP:0006133 calcified artery IAGP N RGD:5509061 20141003 MGI PMID:23994172 733666 Eln elastin gene MP:0006135 artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:14597767 733666 Eln elastin gene MP:0006135 artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:9607766 733666 Eln elastin gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:14597767 733666 Eln elastin gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:14597767 733666 Eln elastin gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:23994172 733666 Eln elastin gene MP:0009862 abnormal aorta elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9819363 733666 Eln elastin gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:9607766 733666 Eln elastin gene MP:0010598 abnormal aortic valve annulus morphology IAGP N RGD:5509061 20141003 MGI PMID:22265892 733666 Eln elastin gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20141003 MGI PMID:9607766 733666 Eln elastin gene MP:0010997 decreased aorta wall thickness IAGP N RGD:5509061 20141003 MGI PMID:14597767 733666 Eln elastin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10970822 733666 Eln elastin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9607766 733666 Eln elastin gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:14597767 733667 Rab29 RAB29, member RAS oncogene family gene MP:0005060 accumulation of giant lysosomes in kidney/renal tubule cells IAGP N RGD:5509061 20240718 MGI PMID:32375042 733667 Rab29 RAB29, member RAS oncogene family gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20240718 MGI PMID:32375042 733667 Rab29 RAB29, member RAS oncogene family gene MP:0030949 abnormal Golgi vesicle transport IAGP N RGD:5509061 20240718 MGI PMID:32375042 733669 Map2 microtubule-associated protein 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:11581286 733669 Map2 microtubule-associated protein 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11581286 733669 Map2 microtubule-associated protein 2 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:11581286 733669 Map2 microtubule-associated protein 2 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:12163474 733669 Map2 microtubule-associated protein 2 gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11581286 733669 Map2 microtubule-associated protein 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12163474 733669 Map2 microtubule-associated protein 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:24501684 733669 Map2 microtubule-associated protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12163474 733669 Map2 microtubule-associated protein 2 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12763072 733669 Map2 microtubule-associated protein 2 gene MP:0001925 male infertility IEA N RGD:5509061 20141003 MGI 733669 Map2 microtubule-associated protein 2 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:11581286 733669 Map2 microtubule-associated protein 2 gene MP:0002208 abnormal germ cell morphology IEA N RGD:5509061 20141003 MGI 733669 Map2 microtubule-associated protein 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11581286 733669 Map2 microtubule-associated protein 2 gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:12763072 733669 Map2 microtubule-associated protein 2 gene MP:0003684 abnormal inferior olivary complex morphology IAGP N RGD:5509061 20141003 MGI PMID:11581286 733669 Map2 microtubule-associated protein 2 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:11581286 733669 Map2 microtubule-associated protein 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:24501684 733669 Map2 microtubule-associated protein 2 gene MP:0005159 azoospermia IEA N RGD:5509061 20141003 MGI 733669 Map2 microtubule-associated protein 2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24501684 733669 Map2 microtubule-associated protein 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:24501684 733669 Map2 microtubule-associated protein 2 gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:11581286 733669 Map2 microtubule-associated protein 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:24501684 733669 Map2 microtubule-associated protein 2 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:24501684 733669 Map2 microtubule-associated protein 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11581286 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0000160 kyphosis IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0001407 short stride length IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0001513 limb grasping IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20230601 MGI 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20150326 MGI PMID:24586861 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20150326 MGI PMID:24586861 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20230601 MGI 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20150326 MGI PMID:24586861 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20150326 MGI PMID:24586861 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0013140 excessive vocalization IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0020358 abnormal inhibitory synapse morphology IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0020361 abnormal symmetric synapse morphology IAGP N RGD:5509061 20170406 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0030691 increased serine level IAGP N RGD:5509061 20180927 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0030697 increased phenylalanine level IAGP N RGD:5509061 20180927 MGI PMID:27912058 733672 Slc7a5 solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 gene MP:0031496 motor developmental delay IAGP N RGD:5509061 20230810 MGI PMID:27912058 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17116638 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17116638 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17116638 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17116638 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:17116638 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17116638 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17116638 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:17116638 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17116638 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:17116638 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17116638 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:17116638 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:17116638 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17116638 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17116638 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 733673 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20231207 MGI 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20160204 MGI PMID:24586179 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20160204 MGI PMID:24586179 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:19864491 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:17267447 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17267447 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19864491 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0001443 poor grooming IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20160204 MGI PMID:24586179 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19864491 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17267447 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19864491 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20141003 MGI PMID:17267447 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19864491 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20160204 MGI PMID:24586179 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20160204 MGI PMID:24586179 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20160204 MGI PMID:24586179 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17267447 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0004857 abnormal heart weight IAGP N RGD:5509061 20160204 MGI PMID:24586179 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160204 MGI PMID:24586179 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:19864491 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:19864491 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19864491 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17267447 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19008300 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230119 MGI 733674 Syne1 spectrin repeat containing, nuclear envelope 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:19864491 733675 Plod1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:17197443 733675 Plod1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17197443 733675 Plod1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17197443 733675 Plod1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17197443 733675 Plod1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 gene MP:0004044 aortic dissection IAGP N RGD:5509061 20141003 MGI PMID:17197443 733675 Plod1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:17197443 733675 Plod1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:17197443 733675 Plod1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20201022 MGI 733675 Plod1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17197443 733675 Plod1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 gene MP:0009866 abnormal aorta wall morphology IAGP N RGD:5509061 20141003 MGI PMID:17197443 733675 Plod1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160421 MGI 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12775763 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12551946 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:12551946 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12775763 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12551946 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12775763 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12551946 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12775763 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0002673 abnormal sperm number IAGP N RGD:5509061 20141003 MGI PMID:12775763 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12551946 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:12775763 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12551946 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12775763 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:12551946 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12551946 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12775763 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:12551946 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:12775763 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12775763 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:12551946 733677 Pafah1b2 platelet-activating factor acetylhydrolase, isoform 1b, subunit 2 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:12775763 733680 Unc5b unc-5 netrin receptor B gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:15510105 733680 Unc5b unc-5 netrin receptor B gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:15510105 733680 Unc5b unc-5 netrin receptor B gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15510105 733680 Unc5b unc-5 netrin receptor B gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15510105 733680 Unc5b unc-5 netrin receptor B gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:15510105 733680 Unc5b unc-5 netrin receptor B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15510105 733680 Unc5b unc-5 netrin receptor B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19004851 733680 Unc5b unc-5 netrin receptor B gene MP:0020327 abnormal capillary branching pattern IAGP N RGD:5509061 20160714 MGI PMID:15510105 733683 Phox2a paired-like homeobox 2a gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:11343120 733683 Phox2a paired-like homeobox 2a gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:21752929 733683 Phox2a paired-like homeobox 2a gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:10882479 733683 Phox2a paired-like homeobox 2a gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:9115735 733683 Phox2a paired-like homeobox 2a gene MP:0001034 abnormal parasympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10882479 733683 Phox2a paired-like homeobox 2a gene MP:0001034 abnormal parasympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9115735 733683 Phox2a paired-like homeobox 2a gene MP:0001035 abnormal submandibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20133851 733683 Phox2a paired-like homeobox 2a gene MP:0001036 small submandibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:10882479 733683 Phox2a paired-like homeobox 2a gene MP:0001036 small submandibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:9115735 733683 Phox2a paired-like homeobox 2a gene MP:0001061 abnormal oculomotor nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16319924 733683 Phox2a paired-like homeobox 2a gene MP:0001063 abnormal trochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16319924 733683 Phox2a paired-like homeobox 2a gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10882479 733683 Phox2a paired-like homeobox 2a gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20133851 733683 Phox2a paired-like homeobox 2a gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:10882479 733683 Phox2a paired-like homeobox 2a gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:9115735 733683 Phox2a paired-like homeobox 2a gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:10882479 733683 Phox2a paired-like homeobox 2a gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:9115735 733683 Phox2a paired-like homeobox 2a gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:10882479 733683 Phox2a paired-like homeobox 2a gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:9115735 733683 Phox2a paired-like homeobox 2a gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:10882479 733683 Phox2a paired-like homeobox 2a gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:9115735 733683 Phox2a paired-like homeobox 2a gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:10882479 733683 Phox2a paired-like homeobox 2a gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11343120 733683 Phox2a paired-like homeobox 2a gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11343120 733683 Phox2a paired-like homeobox 2a gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11343120 733683 Phox2a paired-like homeobox 2a gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:14749437 733683 Phox2a paired-like homeobox 2a gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11343120 733683 Phox2a paired-like homeobox 2a gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11343120 733683 Phox2a paired-like homeobox 2a gene MP:0002751 abnormal autonomic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:10882479 733683 Phox2a paired-like homeobox 2a gene MP:0002751 abnormal autonomic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:9115735 733683 Phox2a paired-like homeobox 2a gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11343120 733683 Phox2a paired-like homeobox 2a gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:11343120 733683 Phox2a paired-like homeobox 2a gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20141003 MGI PMID:10882479 733683 Phox2a paired-like homeobox 2a gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9115735 733683 Phox2a paired-like homeobox 2a gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10882479 733683 Phox2a paired-like homeobox 2a gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:11343120 733683 Phox2a paired-like homeobox 2a gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11343120 733683 Phox2a paired-like homeobox 2a gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11343120 733683 Phox2a paired-like homeobox 2a gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:17218061 733683 Phox2a paired-like homeobox 2a gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:14749437 733683 Phox2a paired-like homeobox 2a gene MP:0005575 increased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:17218061 733683 Phox2a paired-like homeobox 2a gene MP:0005585 increased tidal volume IAGP N RGD:5509061 20141003 MGI PMID:17218061 733683 Phox2a paired-like homeobox 2a gene MP:0008314 abnormal pterygopalatine ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10882479 733683 Phox2a paired-like homeobox 2a gene MP:0008314 abnormal pterygopalatine ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20133851 733683 Phox2a paired-like homeobox 2a gene MP:0008314 abnormal pterygopalatine ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9115735 733683 Phox2a paired-like homeobox 2a gene MP:0008315 abnormal otic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10882479 733683 Phox2a paired-like homeobox 2a gene MP:0008315 abnormal otic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9115735 733683 Phox2a paired-like homeobox 2a gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21752929 733683 Phox2a paired-like homeobox 2a gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:21752929 733683 Phox2a paired-like homeobox 2a gene MP:0010105 abnormal sublingual ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20133851 733683 Phox2a paired-like homeobox 2a gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11343120 733684 Ush2a usherin gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:17360538 733684 Ush2a usherin gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17360538 733684 Ush2a usherin gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:17360538 733684 Ush2a usherin gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:17360538 733684 Ush2a usherin gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17360538 733684 Ush2a usherin gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17360538 733684 Ush2a usherin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:17360538 733684 Ush2a usherin gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:17360538 733684 Ush2a usherin gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:17360538 733687 Slc7a8 solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20111116 MGI 733687 Slc7a8 solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190801 MGI PMID:29355479 733687 Slc7a8 solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 733687 Slc7a8 solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20190801 MGI PMID:29355479 733687 Slc7a8 solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20111116 MGI 733687 Slc7a8 solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 gene MP:0004288 abnormal spiral ligament morphology IAGP N RGD:5509061 20190801 MGI PMID:29355479 733687 Slc7a8 solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 gene MP:0004292 abnormal spiral ligament fibrocyte morphology IAGP N RGD:5509061 20190801 MGI PMID:29355479 733687 Slc7a8 solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20190801 MGI PMID:29355479 733687 Slc7a8 solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 gene MP:0004365 abnormal strial basal cell morphology IAGP N RGD:5509061 20190801 MGI PMID:29355479 733687 Slc7a8 solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20190801 MGI PMID:29355479 733687 Slc7a8 solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20190801 MGI PMID:29355479 733687 Slc7a8 solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 733687 Slc7a8 solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20190801 MGI PMID:29355479 733687 Slc7a8 solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20190801 MGI PMID:29355479 733692 Prx periaxin gene MP:0000344 absent Cajal-Retzius cell IAGP N RGD:5509061 20141003 MGI PMID:23022068 733692 Prx periaxin gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:10839370 733692 Prx periaxin gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:23022068 733692 Prx periaxin gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15356632 733692 Prx periaxin gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22764250 733692 Prx periaxin gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23022068 733692 Prx periaxin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10839370 733692 Prx periaxin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23022068 733692 Prx periaxin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10839370 733692 Prx periaxin gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:10839370 733692 Prx periaxin gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:10839370 733692 Prx periaxin gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:10839370 733692 Prx periaxin gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10839370 733692 Prx periaxin gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20141003 MGI PMID:10839370 733692 Prx periaxin gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:10839370 733692 Prx periaxin gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:10839370 733692 Prx periaxin gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:10839370 733692 Prx periaxin gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:23022068 733692 Prx periaxin gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:10839370 733692 Prx periaxin gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:23022068 733692 Prx periaxin gene MP:0010738 abnormal internode morphology IAGP N RGD:5509061 20141003 MGI PMID:23022068 733692 Prx periaxin gene MP:0010742 increased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:23022068 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:17504941 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:16648472 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:17504941 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:16648472 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16648472 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16648472 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16648472 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16648472 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:16648472 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16648472 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16648472 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0002235 abnormal external nares morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20141003 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0004539 absent maxilla IAGP N RGD:5509061 20141003 MGI PMID:17504941 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:17504941 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0004790 absent upper incisors IAGP N RGD:5509061 20141003 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:16648472 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:16648472 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:17504941 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16648472 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0006290 proboscis IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:16648472 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0009654 abnormal primary palate development IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20221201 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0009897 decreased maxillary shelf size IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16648472 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0012256 abnormal philtrum morphology IAGP N RGD:5509061 20141003 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0012523 abnormal upper lip morphology IAGP N RGD:5509061 20141003 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0012541 absent lamina terminalis IAGP N RGD:5509061 20141003 MGI PMID:16648472 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0013788 external nares atresia IAGP N RGD:5509061 20150611 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0014276 lobar holoprosencephaly IAGP N RGD:5509061 20230810 MGI PMID:21183473 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:17504941 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0030137 abnormal upper incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0030197 small nasal septum IAGP N RGD:5509061 20171012 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0030201 absent nasal septum cartilage IAGP N RGD:5509061 20171012 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0030202 nasal septum cartilage hypoplasia IAGP N RGD:5509061 20171012 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0030218 piriform aperture stenosis IAGP N RGD:5509061 20171019 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0030313 abnormal face development IAGP N RGD:5509061 20171109 MGI PMID:17504941 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0030314 absent primary palate IAGP N RGD:5509061 20171109 MGI PMID:12620190 733697 Cdon cell adhesion molecule-related/down-regulated by oncogenes gene MP:0030314 absent primary palate IAGP N RGD:5509061 20171109 MGI PMID:21183473 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0000098 abnormal vomer bone morphology IAGP N RGD:5509061 20230420 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0000101 absent ethmoid bone IAGP N RGD:5509061 20230420 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20230420 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20230420 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20230420 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20230420 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20230420 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20230420 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20230420 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0010030 abnormal orbit morphology IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0010410 cor triatriatum sinistrum IAGP N RGD:5509061 20230420 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0010701 fusion of atlas and odontoid process IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20230420 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0011615 submucous cleft palate IAGP N RGD:5509061 20230420 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20230420 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210218 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0013201 head mesenchyme hyperplasia IAGP N RGD:5509061 20230420 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0014427 increased circulating hyaluronic acid level IAGP N RGD:5509061 20240425 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0014429 increased hyaluronic acid level IAGP N RGD:5509061 20240425 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0021164 oral cleft IAGP N RGD:5509061 20230420 MGI PMID:28081210 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0030030 Wormian bones IAGP N RGD:5509061 20221110 MGI PMID:18772348 733699 Hyal2 hyaluronoglucosaminidase 2 gene MP:0030303 small ethmoid bone IAGP N RGD:5509061 20230420 MGI PMID:28081210 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:19225127 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19225127 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0001340 abnormal eyelid morphology IEA N RGD:5509061 20201022 MGI 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201022 MGI 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210128 MGI 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19225127 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20240523 MGI 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0005102 abnormal iris pigmentation IEA N RGD:5509061 20201022 MGI 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20240523 MGI 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20240523 MGI 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20240523 MGI 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0012121 sclerocornea IEA N RGD:5509061 20240523 MGI 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 733701 Epb41l1 erythrocyte membrane protein band 4.1 like 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15777780 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:11923483 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20141003 MGI PMID:10801976 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20141003 MGI PMID:11854466 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:10801976 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:10801976 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11102459 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11923483 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:15630454 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0002711 decreased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:15777780 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:11854466 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:11923483 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15630454 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:11854466 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0003488 decreased channel response intensity IAGP N RGD:5509061 20141003 MGI PMID:12154172 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0003489 increased channel response threshold IAGP N RGD:5509061 20141003 MGI PMID:12154172 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15630454 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0003565 abnormal glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:15630454 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11923483 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15630454 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15630454 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15777780 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15777780 733703 Cacna1e calcium channel, voltage-dependent, R type, alpha 1E subunit gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:15630454 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0001393 ataxia IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0002083 premature death IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0002763 ectopic Bergmann glia cells IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0008569 lethality at weaning IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0009978 abnormal cerebellum white matter morphology IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0010892 increased oligodendrocyte progenitor number IAGP N RGD:5509061 20180628 MGI PMID:26974157 733708 Eif2b4 eukaryotic translation initiation factor 2B, subunit 4 delta gene MP:0014429 increased hyaluronic acid level IAGP N RGD:5509061 20240425 MGI PMID:26974157 733709 Sycn syncollin gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:11839820 733709 Sycn syncollin gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20141003 MGI PMID:11839820 733709 Sycn syncollin gene MP:0031325 delayed pancreas regeneration IAGP N RGD:5509061 20220106 MGI PMID:11839820 733713 Atf4 activating transcription factor 4 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15109498 733713 Atf4 activating transcription factor 4 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15109498 733713 Atf4 activating transcription factor 4 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15109498 733713 Atf4 activating transcription factor 4 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15109498 733713 Atf4 activating transcription factor 4 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20230119 MGI 733713 Atf4 activating transcription factor 4 gene MP:0000239 absent common myeloid progenitor cells IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 733713 Atf4 activating transcription factor 4 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20170105 MGI PMID:27812542 733713 Atf4 activating transcription factor 4 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 733713 Atf4 activating transcription factor 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19726872 733713 Atf4 activating transcription factor 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10885750 733713 Atf4 activating transcription factor 4 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10096021 733713 Atf4 activating transcription factor 4 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10885750 733713 Atf4 activating transcription factor 4 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:10885750 733713 Atf4 activating transcription factor 4 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:10885750 733713 Atf4 activating transcription factor 4 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:14561648 733713 Atf4 activating transcription factor 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:17727724 733713 Atf4 activating transcription factor 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19726872 733713 Atf4 activating transcription factor 4 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19726872 733713 Atf4 activating transcription factor 4 gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:14561648 733713 Atf4 activating transcription factor 4 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10096021 733713 Atf4 activating transcription factor 4 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10885750 733713 Atf4 activating transcription factor 4 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19726872 733713 Atf4 activating transcription factor 4 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:15109498 733713 Atf4 activating transcription factor 4 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20230119 MGI 733713 Atf4 activating transcription factor 4 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19726872 733713 Atf4 activating transcription factor 4 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:10885750 733713 Atf4 activating transcription factor 4 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16751105 733713 Atf4 activating transcription factor 4 gene MP:0004064 decreased susceptibility to induced muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:22692209 733713 Atf4 activating transcription factor 4 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:10885750 733713 Atf4 activating transcription factor 4 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20170105 MGI PMID:27812542 733713 Atf4 activating transcription factor 4 gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20141003 MGI PMID:10885750 733713 Atf4 activating transcription factor 4 gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20141003 MGI PMID:10885750 733713 Atf4 activating transcription factor 4 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19726872 733713 Atf4 activating transcription factor 4 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15109498 733713 Atf4 activating transcription factor 4 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230119 MGI 733713 Atf4 activating transcription factor 4 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19726872 733713 Atf4 activating transcription factor 4 gene MP:0005492 exocrine pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15109498 733713 Atf4 activating transcription factor 4 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19726872 733713 Atf4 activating transcription factor 4 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15109498 733713 Atf4 activating transcription factor 4 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:17727724 733713 Atf4 activating transcription factor 4 gene MP:0008794 increased lens epithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10096021 733713 Atf4 activating transcription factor 4 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19726872 733713 Atf4 activating transcription factor 4 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:19726872 733713 Atf4 activating transcription factor 4 gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:17727724 733713 Atf4 activating transcription factor 4 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17727724 733713 Atf4 activating transcription factor 4 gene MP:0009160 abnormal pancreatic acinar cell zymogen granule morphology IAGP N RGD:5509061 20141003 MGI PMID:17727724 733713 Atf4 activating transcription factor 4 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23945236 733713 Atf4 activating transcription factor 4 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:15109498 733713 Atf4 activating transcription factor 4 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:16751105 733713 Atf4 activating transcription factor 4 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:23945236 733713 Atf4 activating transcription factor 4 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:16751105 733713 Atf4 activating transcription factor 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10096021 733713 Atf4 activating transcription factor 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10885750 733713 Atf4 activating transcription factor 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11806972 733713 Atf4 activating transcription factor 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 733713 Atf4 activating transcription factor 4 gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20150611 MGI PMID:19726872 733713 Atf4 activating transcription factor 4 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:23945236 733713 Atf4 activating transcription factor 4 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:16751105 733713 Atf4 activating transcription factor 4 gene MP:0030388 large fontanelles IAGP N RGD:5509061 20171207 MGI PMID:15109498 733713 Atf4 activating transcription factor 4 gene MP:0030973 impaired gluconeogenesis IAGP N RGD:5509061 20200102 MGI PMID:19726872 733717 Hmgcl 3-hydroxy-3-methylglutaryl-Coenzyme A lyase gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:23861731 733717 Hmgcl 3-hydroxy-3-methylglutaryl-Coenzyme A lyase gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:9817922 733717 Hmgcl 3-hydroxy-3-methylglutaryl-Coenzyme A lyase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9817922 733717 Hmgcl 3-hydroxy-3-methylglutaryl-Coenzyme A lyase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9817922 733717 Hmgcl 3-hydroxy-3-methylglutaryl-Coenzyme A lyase gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:9817922 733717 Hmgcl 3-hydroxy-3-methylglutaryl-Coenzyme A lyase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23861731 733717 Hmgcl 3-hydroxy-3-methylglutaryl-Coenzyme A lyase gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:23861731 733717 Hmgcl 3-hydroxy-3-methylglutaryl-Coenzyme A lyase gene MP:0003979 increased circulating carnitine level IAGP N RGD:5509061 20141003 MGI PMID:23861731 733717 Hmgcl 3-hydroxy-3-methylglutaryl-Coenzyme A lyase gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:23861731 733717 Hmgcl 3-hydroxy-3-methylglutaryl-Coenzyme A lyase gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:23861731 733717 Hmgcl 3-hydroxy-3-methylglutaryl-Coenzyme A lyase gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23861731 733717 Hmgcl 3-hydroxy-3-methylglutaryl-Coenzyme A lyase gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9817922 733717 Hmgcl 3-hydroxy-3-methylglutaryl-Coenzyme A lyase gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:23861731 733717 Hmgcl 3-hydroxy-3-methylglutaryl-Coenzyme A lyase gene MP:0014341 abnormal hepatocyte mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:9817922 733719 Anxa6 annexin A6 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20151126 MGI PMID:22692895 733719 Anxa6 annexin A6 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 733719 Anxa6 annexin A6 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20160804 MGI 733719 Anxa6 annexin A6 gene MP:0002697 abnormal eye size IEA N RGD:5509061 20160804 MGI 733719 Anxa6 annexin A6 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20151126 MGI PMID:22692895 733719 Anxa6 annexin A6 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20151126 MGI PMID:22692895 733719 Anxa6 annexin A6 gene MP:0005600 increased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11919174 733719 Anxa6 annexin A6 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160804 MGI 733719 Anxa6 annexin A6 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20151126 MGI PMID:22692895 733719 Anxa6 annexin A6 gene MP:0013763 increased T-helper cell number IAGP N RGD:5509061 20151126 MGI PMID:22692895 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9177182 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9177182 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9177182 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:9177182 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:9177182 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9177182 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0010091 decreased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0011891 decreased circulating ferritin level IAGP N RGD:5509061 20141003 MGI PMID:9482793 733721 Pcmt1 protein-L-isoaspartate (D-aspartate) O-methyltransferase 1 gene MP:0011972 decreased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210211 MGI PMID:9482793 733722 Pax4 paired box 4 gene MP:0000745 tremors IEA N RGD:5509061 20210826 MGI 733722 Pax4 paired box 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18058910 733722 Pax4 paired box 4 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:18058910 733722 Pax4 paired box 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22717987 733722 Pax4 paired box 4 gene MP:0002694 abnormal pancreas secretion IAGP N RGD:5509061 20141003 MGI PMID:9121556 733722 Pax4 paired box 4 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 733722 Pax4 paired box 4 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:9121556 733722 Pax4 paired box 4 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:9163426 733722 Pax4 paired box 4 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20160421 MGI 733722 Pax4 paired box 4 gene MP:0009174 absent pancreatic beta cells IAGP N RGD:5509061 20141003 MGI PMID:18058910 733722 Pax4 paired box 4 gene MP:0009174 absent pancreatic beta cells IAGP N RGD:5509061 20141003 MGI PMID:22717987 733722 Pax4 paired box 4 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:22717987 733722 Pax4 paired box 4 gene MP:0009182 absent pancreatic delta cells IAGP N RGD:5509061 20141003 MGI PMID:18058910 733722 Pax4 paired box 4 gene MP:0009182 absent pancreatic delta cells IAGP N RGD:5509061 20141003 MGI PMID:22717987 733722 Pax4 paired box 4 gene MP:0009182 absent pancreatic delta cells IAGP N RGD:5509061 20141003 MGI PMID:9021175 733722 Pax4 paired box 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18058910 733722 Pax4 paired box 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9121556 733722 Pax4 paired box 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22717987 733722 Pax4 paired box 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22717987 733722 Pax4 paired box 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733726 Slc6a13 solute carrier family 6 (neurotransmitter transporter, GABA), member 13 gene MP:0030635 increased taurine level IAGP N RGD:5509061 20180913 MGI PMID:22896705 733726 Slc6a13 solute carrier family 6 (neurotransmitter transporter, GABA), member 13 gene MP:0030636 decreased taurine level IAGP N RGD:5509061 20180913 MGI PMID:22896705 733728 Ppp1r17 protein phosphatase 1, regulatory subunit 17 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230601 MGI 733728 Ppp1r17 protein phosphatase 1, regulatory subunit 17 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 733730 Mlh1 mutL homolog 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:8673133 733730 Mlh1 mutL homolog 1 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:8673133 733730 Mlh1 mutL homolog 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:8674118 733730 Mlh1 mutL homolog 1 gene MP:0001304 cataract IEA N RGD:5509061 20221215 MGI 733730 Mlh1 mutL homolog 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8674118 733730 Mlh1 mutL homolog 1 gene MP:0001800 abnormal humoral immune response IEA N RGD:5509061 20181011 MGI 733730 Mlh1 mutL homolog 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18337503 733730 Mlh1 mutL homolog 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8673133 733730 Mlh1 mutL homolog 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8674118 733730 Mlh1 mutL homolog 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18337503 733730 Mlh1 mutL homolog 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8673133 733730 Mlh1 mutL homolog 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8674118 733730 Mlh1 mutL homolog 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 733730 Mlh1 mutL homolog 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18337503 733730 Mlh1 mutL homolog 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9560238 733730 Mlh1 mutL homolog 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 733730 Mlh1 mutL homolog 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15700306 733730 Mlh1 mutL homolog 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 733730 Mlh1 mutL homolog 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 733730 Mlh1 mutL homolog 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9560238 733730 Mlh1 mutL homolog 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 733730 Mlh1 mutL homolog 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9560238 733730 Mlh1 mutL homolog 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10096563 733730 Mlh1 mutL homolog 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11940649 733730 Mlh1 mutL homolog 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15700306 733730 Mlh1 mutL homolog 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18337503 733730 Mlh1 mutL homolog 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19805137 733730 Mlh1 mutL homolog 1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11940649 733730 Mlh1 mutL homolog 1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 733730 Mlh1 mutL homolog 1 gene MP:0002492 decreased IgE level IEA N RGD:5509061 20181011 MGI 733730 Mlh1 mutL homolog 1 gene MP:0002494 increased IgM level IEA N RGD:5509061 20181011 MGI 733730 Mlh1 mutL homolog 1 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:8673133 733730 Mlh1 mutL homolog 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:18337503 733730 Mlh1 mutL homolog 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 733730 Mlh1 mutL homolog 1 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11940649 733730 Mlh1 mutL homolog 1 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 733730 Mlh1 mutL homolog 1 gene MP:0003292 melena IAGP N RGD:5509061 20141003 MGI PMID:10096563 733730 Mlh1 mutL homolog 1 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 733730 Mlh1 mutL homolog 1 gene MP:0004208 increased basal cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18337503 733730 Mlh1 mutL homolog 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 733730 Mlh1 mutL homolog 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:8673133 733730 Mlh1 mutL homolog 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:8674118 733730 Mlh1 mutL homolog 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:8674118 733730 Mlh1 mutL homolog 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18337503 733730 Mlh1 mutL homolog 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 733730 Mlh1 mutL homolog 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:18337503 733730 Mlh1 mutL homolog 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:8673133 733730 Mlh1 mutL homolog 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:8674118 733730 Mlh1 mutL homolog 1 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 733730 Mlh1 mutL homolog 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18337503 733730 Mlh1 mutL homolog 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:18337503 733730 Mlh1 mutL homolog 1 gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20151015 MGI PMID:25533956 733730 Mlh1 mutL homolog 1 gene MP:0009222 increased uterus tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11940649 733730 Mlh1 mutL homolog 1 gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 733730 Mlh1 mutL homolog 1 gene MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18337503 733730 Mlh1 mutL homolog 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20151015 MGI PMID:25533956 733730 Mlh1 mutL homolog 1 gene MP:0009761 abnormal meiotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:18337503 733730 Mlh1 mutL homolog 1 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 733730 Mlh1 mutL homolog 1 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18337503 733730 Mlh1 mutL homolog 1 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 733730 Mlh1 mutL homolog 1 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11940649 733730 Mlh1 mutL homolog 1 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18337503 733730 Mlh1 mutL homolog 1 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 733730 Mlh1 mutL homolog 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19805137 733730 Mlh1 mutL homolog 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11940649 733730 Mlh1 mutL homolog 1 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19805137 733730 Mlh1 mutL homolog 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10096563 733730 Mlh1 mutL homolog 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11940649 733730 Mlh1 mutL homolog 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18337503 733730 Mlh1 mutL homolog 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 733730 Mlh1 mutL homolog 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8673133 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12910267 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:12910267 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0001830 decreased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12910267 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16862125 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17486093 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12910267 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0002494 increased IgM level IEA N RGD:5509061 20181011 MGI 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0002497 increased IgE level IEA N RGD:5509061 20181011 MGI 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17486093 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0004838 abnormal neural fold elevation formation IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12910267 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0005015 increased T cell number IEA N RGD:5509061 20181011 MGI 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12910267 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12910267 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14614861 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14614861 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0008082 increased single-positive T cell number IEA N RGD:5509061 20181011 MGI 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:12910267 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12910267 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12910267 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12910267 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11163238 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12910267 733736 Bcl10 B cell leukemia/lymphoma 10 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11163238 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:8812411 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:9238094 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:17251442 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:21617753 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:21617753 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:9238094 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:17251442 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:21617753 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0002579 disorganized secondary lens fibers IAGP N RGD:5509061 20141003 MGI PMID:9238094 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0002697 abnormal eye size IAGP N RGD:5509061 20141003 MGI PMID:21617753 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:9238094 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21617753 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9238094 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20141003 MGI PMID:9238094 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:21617753 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0010263 total cataract IAGP N RGD:5509061 20141003 MGI PMID:8812411 733737 Lim2 lens intrinsic membrane protein 2 gene MP:0011697 lens vacuoles IAGP N RGD:5509061 20141003 MGI PMID:9238094 733738 Faim2 Fas apoptotic inhibitory molecule 2 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20111116 MGI 733738 Faim2 Fas apoptotic inhibitory molecule 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 733738 Faim2 Fas apoptotic inhibitory molecule 2 gene MP:0000692 small spleen IEA N RGD:5509061 20240523 MGI 733738 Faim2 Fas apoptotic inhibitory molecule 2 gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 733738 Faim2 Fas apoptotic inhibitory molecule 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20111116 MGI 733738 Faim2 Fas apoptotic inhibitory molecule 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20111116 MGI 733738 Faim2 Fas apoptotic inhibitory molecule 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20111116 MGI 733738 Faim2 Fas apoptotic inhibitory molecule 2 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20111116 MGI 733738 Faim2 Fas apoptotic inhibitory molecule 2 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:21209208 733743 Dgkg diacylglycerol kinase, gamma gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200723 MGI PMID:32033984 733743 Dgkg diacylglycerol kinase, gamma gene MP:0001407 short stride length IAGP N RGD:5509061 20200723 MGI PMID:32033984 733743 Dgkg diacylglycerol kinase, gamma gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20200723 MGI PMID:32033984 733743 Dgkg diacylglycerol kinase, gamma gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20200723 MGI PMID:32033984 733743 Dgkg diacylglycerol kinase, gamma gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20200723 MGI PMID:32033984 733743 Dgkg diacylglycerol kinase, gamma gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20200723 MGI PMID:32033984 733745 Prdx1 peroxiredoxin 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20210701 MGI PMID:32736685 733745 Prdx1 peroxiredoxin 1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0002619 abnormal lymphocyte morphology IEA N RGD:5509061 20111116 MGI 733745 Prdx1 peroxiredoxin 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20141003 MGI PMID:16297875 733745 Prdx1 peroxiredoxin 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0003430 increased pancreatic islet cell adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20210701 MGI PMID:32736685 733745 Prdx1 peroxiredoxin 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0008038 abnormal NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0008850 increased hemoglobin concentration distribution width IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0009580 increased keratinocyte apoptosis IAGP N RGD:5509061 20210701 MGI PMID:32736685 733745 Prdx1 peroxiredoxin 1 gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210211 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0012664 decreased circulating haptoglobin level IAGP N RGD:5509061 20210211 MGI PMID:12891360 733745 Prdx1 peroxiredoxin 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:12891360 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:15545996 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20190613 MGI PMID:15780748 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20190613 MGI PMID:15780748 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11877258 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:24880340 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20190613 MGI PMID:15780748 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11877258 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15545996 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23040355 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:24880340 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0001577 anemia IAGP N RGD:5509061 20150611 MGI PMID:19734452 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0001577 anemia IAGP N RGD:5509061 20190613 MGI PMID:15780748 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0001586 abnormal erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002224 abnormal spleen size IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:24880340 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15545996 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:15545996 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:24880340 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20190613 MGI PMID:15780748 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20190613 MGI PMID:15780748 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:15545996 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002642 anisocytosis IAGP N RGD:5509061 20190613 MGI PMID:15780748 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20190613 MGI PMID:15780748 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20190613 MGI PMID:15780748 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20190613 MGI PMID:15780748 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:15545996 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:24880340 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:24880340 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20190613 MGI PMID:15780748 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20190613 MGI PMID:15780748 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:24880340 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0005563 abnormal hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20141003 MGI PMID:11877258 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0008738 abnormal liver iron level IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0008739 abnormal spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:24880340 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0008850 increased hemoglobin concentration distribution width IAGP N RGD:5509061 20141003 MGI PMID:15545996 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0008941 reticulocytopenia IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15545996 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20190613 MGI PMID:15780748 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8524813 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20190613 MGI PMID:15780748 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23040355 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15545996 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0011171 increased number of Heinz bodies IAGP N RGD:5509061 20141003 MGI PMID:15545996 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20150611 MGI PMID:19734452 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0011284 abnormal circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:22490684 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:24880340 733746 Hbb-b2 hemoglobin, beta adult minor chain gene MP:0011913 abnormal reticulocyte cell number IAGP N RGD:5509061 20150611 MGI PMID:19734452 733749 Ptprr protein tyrosine phosphatase receptor type R gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17266727 733749 Ptprr protein tyrosine phosphatase receptor type R gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17266727 733749 Ptprr protein tyrosine phosphatase receptor type R gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:17266727 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22326220 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22941110 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:22941110 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:22326220 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15753128 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:15753128 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22941110 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16675849 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:22326220 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22941110 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19456252 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:15956119 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22941110 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16675849 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15753128 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:22326220 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:15753128 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:22326220 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:18414683 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:18414683 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22326220 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:18414683 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:22326220 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18414683 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:18414683 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0005251 blepharitis IAGP N RGD:5509061 20141003 MGI PMID:15753128 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0005260 ocular hypotension IAGP N RGD:5509061 20141003 MGI PMID:19456252 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22941110 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:18414683 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22941110 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:22326220 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:23877263 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18414683 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22941110 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22941110 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22941110 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22941110 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19456252 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15753128 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0011103 embryonic lethality at implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16675849 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20170105 MGI 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:22326220 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0011369 increased renal glomerulus apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22326220 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:22326220 733752 Rock1 Rho-associated coiled-coil containing protein kinase 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:22941110 733753 Gyg1 glycogenin 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20220331 MGI PMID:33219378 733753 Gyg1 glycogenin 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20220331 MGI PMID:33219378 733753 Gyg1 glycogenin 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20220331 MGI PMID:33219378 733753 Gyg1 glycogenin 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20231207 MGI 733753 Gyg1 glycogenin 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20220331 MGI PMID:33219378 733753 Gyg1 glycogenin 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20220331 MGI PMID:33219378 733753 Gyg1 glycogenin 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20220331 MGI PMID:33219378 733753 Gyg1 glycogenin 1 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20231207 MGI 733753 Gyg1 glycogenin 1 gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0004609 vertebral fusion IEA N RGD:5509061 20231207 MGI 733753 Gyg1 glycogenin 1 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20231207 MGI 733753 Gyg1 glycogenin 1 gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0010889 small alveolar lamellar bodies IAGP N RGD:5509061 20220331 MGI PMID:33219378 733753 Gyg1 glycogenin 1 gene MP:0010951 abnormal lipid oxidation IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20220331 MGI PMID:33219378 733753 Gyg1 glycogenin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 733753 Gyg1 glycogenin 1 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0012735 abnormal response to exercise IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0014071 increased cardiac muscle glycogen level IAGP N RGD:5509061 20190131 MGI PMID:28683291 733753 Gyg1 glycogenin 1 gene MP:0031007 decreased lung glycogen level IAGP N RGD:5509061 20220331 MGI PMID:33219378 733756 Mmp3 matrix metallopeptidase 3 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:15044844 733756 Mmp3 matrix metallopeptidase 3 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15618213 733756 Mmp3 matrix metallopeptidase 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15470062 733756 Mmp3 matrix metallopeptidase 3 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:10450741 733756 Mmp3 matrix metallopeptidase 3 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:9433876 733756 Mmp3 matrix metallopeptidase 3 gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:9433876 733756 Mmp3 matrix metallopeptidase 3 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:9433876 733756 Mmp3 matrix metallopeptidase 3 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10359808 733756 Mmp3 matrix metallopeptidase 3 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:15044844 733756 Mmp3 matrix metallopeptidase 3 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:11350822 733756 Mmp3 matrix metallopeptidase 3 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15470062 733756 Mmp3 matrix metallopeptidase 3 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10359808 733757 Mmp10 matrix metallopeptidase 10 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17923522 733757 Mmp10 matrix metallopeptidase 10 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17923522 733757 Mmp10 matrix metallopeptidase 10 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 733757 Mmp10 matrix metallopeptidase 10 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17923522 733762 Slk STE20-like kinase gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0000962 disorganized dorsal root ganglion IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 733762 Slk STE20-like kinase gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0001914 hemorrhage IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0002080 prenatal lethality IEA N RGD:5509061 20230601 MGI 733762 Slk STE20-like kinase gene MP:0002574 increased vertical activity IEA N RGD:5509061 20230601 MGI 733762 Slk STE20-like kinase gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0005238 increased brain size IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0008957 abnormal placenta junctional zone morphology IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0009658 increased placenta apoptosis IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 733762 Slk STE20-like kinase gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20151112 MGI PMID:24868594 733762 Slk STE20-like kinase gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20151112 MGI PMID:24868594 733763 Cyp2f2 cytochrome P450, family 2, subfamily f, polypeptide 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 733763 Cyp2f2 cytochrome P450, family 2, subfamily f, polypeptide 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22397853 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000022 abnormal ear shape IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000023 abnormal ear position IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:17541405 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17541405 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:16954348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16954348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19424505 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:10974002 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:16954348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000381 enlarged hair follicles IAGP N RGD:5509061 20141003 MGI PMID:23702582 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16954348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:19424505 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:23702582 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20170921 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:17088430 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17088430 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17088430 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:17088430 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:17088430 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:17088430 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21098262 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000525 renal tubular acidosis IAGP N RGD:5509061 20141003 MGI PMID:21098262 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:15889143 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000648 absent sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:15253938 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11516395 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:11516395 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:11516395 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:11516395 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:11516395 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:11516395 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:23100420 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:11516395 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23100420 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15253938 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11516395 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16571628 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:15253938 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:15253938 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15253938 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001109 absent Schwann cell precursors IAGP N RGD:5509061 20141003 MGI PMID:15253938 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:16954348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:10974002 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:10974002 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:10974002 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:16954348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:19424505 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:16954348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10974002 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23702582 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:10974002 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:16954348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19424505 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:10974002 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19424505 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17088430 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17541405 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17493607 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:11516395 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11516395 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:15253938 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:17088430 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:22561348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001727 abnormal embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:22561348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11516395 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:19424505 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:16954348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:23702582 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11516395 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15253938 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16954348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:17541405 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16954348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:16571628 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:15253938 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18451854 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15253938 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:22561348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:7544312 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:17344408 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:23100420 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002791 steatorrhea IAGP N RGD:5509061 20141003 MGI PMID:17088430 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17493607 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:23702582 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20141003 MGI PMID:16571628 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003017 decreased circulating bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:21098262 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:17493607 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17493607 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:17541405 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:17541405 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003626 kidney medulla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:15253938 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003648 abnormal radial glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21185282 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:10974002 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:16954348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003794 delayed somite formation IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:17088430 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004039 abnormal cardiac muscle cell glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:17541405 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:10974002 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:17344408 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:21876123 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004867 decreased platelet calcium level IAGP N RGD:5509061 20141003 MGI PMID:12586747 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004963 abnormal blastocoele morphology IAGP N RGD:5509061 20141003 MGI PMID:7544312 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004964 absent inner cell mass IAGP N RGD:5509061 20141003 MGI PMID:16618804 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:7544312 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7544312 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0005035 perianal ulcer IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:12586747 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:16618804 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0005556 abnormal renal filtration rate IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23702582 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0005623 abnormal meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:11516395 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0005664 decreased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:16618804 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:16571628 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:15889143 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:17541405 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:17088430 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0008030 abnormal Cajal-Retzius cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11516395 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0008030 abnormal Cajal-Retzius cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21185282 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20141003 MGI PMID:19424505 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:17541405 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:17541405 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0009267 abnormal cerebellum fissure morphology IAGP N RGD:5509061 20141003 MGI PMID:23100420 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0009349 increased urine pH IAGP N RGD:5509061 20141003 MGI PMID:21098262 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0009385 abnormal dermal pigmentation IAGP N RGD:5509061 20141003 MGI PMID:19424505 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19424505 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23702582 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:18451854 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0009964 abnormal cerebellum lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:23100420 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15324699 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0010334 pleural effusion IAGP N RGD:5509061 20141003 MGI PMID:11884376 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0010387 abnormal Bergmann glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23100420 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0010684 abnormal hair follicle outer root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:19424505 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17088430 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11516395 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10974002 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16954348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23702582 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7544313 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16618804 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19424505 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7544312 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16954348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22561348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011159 abnormal epidermal-dermal junction morphology IAGP N RGD:5509061 20141003 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011159 abnormal epidermal-dermal junction morphology IAGP N RGD:5509061 20141003 MGI PMID:19424505 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20141003 MGI PMID:10974002 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:7544312 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011264 abnormal cardiac mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011282 increased podocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22561348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011417 abnormal renal transport IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011509 dilated glomerular capillary IAGP N RGD:5509061 20141003 MGI PMID:18328474 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:11980921 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0012194 decreased keratinocyte migration IAGP N RGD:5509061 20141003 MGI PMID:23702582 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0012263 decreased hindbrain size IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20170921 MGI PMID:21098262 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0012702 increased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:9553049 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0013001 abnormal enteric neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16571628 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0013006 abnormal enteric neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:16571628 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0013305 isosthenuria IAGP N RGD:5509061 20141120 MGI PMID:19439520 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20171221 MGI PMID:14522949 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0020391 radial glial endfoot detachment IAGP N RGD:5509061 20161117 MGI PMID:21185282 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0030575 decreased hair follicle cell proliferation IAGP N RGD:5509061 20181129 MGI PMID:10921880 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0030578 decreased keratinocyte adhesion IAGP N RGD:5509061 20180607 MGI PMID:16954348 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0030578 decreased keratinocyte adhesion IAGP N RGD:5509061 20180607 MGI PMID:21876123 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0030578 decreased keratinocyte adhesion IAGP N RGD:5509061 20180607 MGI PMID:23702582 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0030956 abnormal neuronal precursor cell migration IAGP N RGD:5509061 20190725 MGI PMID:17344408 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0030957 abnormal myotube morphology IAGP N RGD:5509061 20190725 MGI PMID:12620989 733764 Itgb1 integrin beta 1 (fibronectin receptor beta) gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:11884376 733767 Ybx3 Y box protein 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16954378 733767 Ybx3 Y box protein 3 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:16954378 733767 Ybx3 Y box protein 3 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:16954378 733767 Ybx3 Y box protein 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16954378 733767 Ybx3 Y box protein 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16954378 733767 Ybx3 Y box protein 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16954378 733767 Ybx3 Y box protein 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16954378 733767 Ybx3 Y box protein 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 733767 Ybx3 Y box protein 3 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16954378 733767 Ybx3 Y box protein 3 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 733767 Ybx3 Y box protein 3 gene MP:0004002 abnormal jejunum morphology IEA N RGD:5509061 20210520 MGI 733767 Ybx3 Y box protein 3 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:16954378 733767 Ybx3 Y box protein 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16954378 733768 Lss lanosterol synthase gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 733768 Lss lanosterol synthase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20170105 MGI 733768 Lss lanosterol synthase gene MP:0001306 small lens IAGP N RGD:5509061 20220120 MGI PMID:34926465 733768 Lss lanosterol synthase gene MP:0002579 disorganized secondary lens fibers IAGP N RGD:5509061 20220120 MGI PMID:34926465 733768 Lss lanosterol synthase gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20220120 MGI PMID:34926465 733768 Lss lanosterol synthase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 733768 Lss lanosterol synthase gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20220120 MGI PMID:34926465 733768 Lss lanosterol synthase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20220120 MGI PMID:34926465 733768 Lss lanosterol synthase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733768 Lss lanosterol synthase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 733768 Lss lanosterol synthase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 733768 Lss lanosterol synthase gene MP:0031345 developmental cataract IAGP N RGD:5509061 20220217 MGI PMID:34926465 733769 Nxph4 neurexophilin 4 gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20141003 MGI 733769 Nxph4 neurexophilin 4 gene MP:0011741 increased urine nitrite level IEA N RGD:5509061 20141003 MGI 733770 Akr1d1 aldo-keto reductase family 1, member D1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 733770 Akr1d1 aldo-keto reductase family 1, member D1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 733770 Akr1d1 aldo-keto reductase family 1, member D1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220811 MGI 733770 Akr1d1 aldo-keto reductase family 1, member D1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20181227 MGI 733770 Akr1d1 aldo-keto reductase family 1, member D1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 733775 Clta clathrin light chain A gene MP:0001405 impaired coordination IAGP N RGD:5509061 20230216 MGI PMID:32907943 733775 Clta clathrin light chain A gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20230216 MGI PMID:32907943 733775 Clta clathrin light chain A gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20230216 MGI PMID:32907943 733775 Clta clathrin light chain A gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20230216 MGI PMID:32907943 733775 Clta clathrin light chain A gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20230216 MGI PMID:32907943 733775 Clta clathrin light chain A gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20230216 MGI PMID:32907943 733775 Clta clathrin light chain A gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20220825 MGI PMID:27540116 733775 Clta clathrin light chain A gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20220825 MGI PMID:27540116 733775 Clta clathrin light chain A gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20230216 MGI PMID:32907943 733775 Clta clathrin light chain A gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20220825 MGI PMID:27540116 733775 Clta clathrin light chain A gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20230216 MGI PMID:32907943 733777 Fgf22 fibroblast growth factor 22 gene MP:0001406 abnormal gait IEA N RGD:5509061 20220811 MGI 733777 Fgf22 fibroblast growth factor 22 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:20505669 733777 Fgf22 fibroblast growth factor 22 gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:20505669 733777 Fgf22 fibroblast growth factor 22 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:20505669 733777 Fgf22 fibroblast growth factor 22 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22737238 733777 Fgf22 fibroblast growth factor 22 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20505669 733777 Fgf22 fibroblast growth factor 22 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:20505669 733777 Fgf22 fibroblast growth factor 22 gene MP:0004793 abnormal synaptic vesicle clustering IAGP N RGD:5509061 20141003 MGI PMID:20505669 733777 Fgf22 fibroblast growth factor 22 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 733777 Fgf22 fibroblast growth factor 22 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:20505669 733780 Rph3a rabphilin 3A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10407024 733780 Rph3a rabphilin 3A gene MP:0002915 abnormal synaptic depression IAGP N RGD:5509061 20241031 MGI PMID:33753311 733780 Rph3a rabphilin 3A gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20241031 MGI PMID:33753311 733780 Rph3a rabphilin 3A gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20241031 MGI PMID:33753311 733780 Rph3a rabphilin 3A gene MP:0008921 increased neurotransmitter release IAGP N RGD:5509061 20241031 MGI PMID:33753311 733780 Rph3a rabphilin 3A gene MP:0014253 decreased paired-pulse ratio IAGP N RGD:5509061 20241031 MGI PMID:33753311 733782 Gja3 gap junction protein, alpha 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:16611690 733782 Gja3 gap junction protein, alpha 3 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:16611690 733782 Gja3 gap junction protein, alpha 3 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20160505 MGI PMID:25103261 733782 Gja3 gap junction protein, alpha 3 gene MP:0001304 cataract IAGP N RGD:5509061 20160505 MGI PMID:25103261 733782 Gja3 gap junction protein, alpha 3 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:16611690 733782 Gja3 gap junction protein, alpha 3 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:23300808 733782 Gja3 gap junction protein, alpha 3 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20160505 MGI PMID:25103261 733784 Adam3 ADAM metallopeptidase domain 3 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:11319869 733784 Adam3 ADAM metallopeptidase domain 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10569988 733784 Adam3 ADAM metallopeptidase domain 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11319869 733784 Adam3 ADAM metallopeptidase domain 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20190926 MGI PMID:30209135 733784 Adam3 ADAM metallopeptidase domain 3 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191017 MGI PMID:11319869 733784 Adam3 ADAM metallopeptidase domain 3 gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:10569988 733785 Crisp2 cysteine-rich secretory protein 2 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 733785 Crisp2 cysteine-rich secretory protein 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240627 MGI 733785 Crisp2 cysteine-rich secretory protein 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20191114 MGI PMID:30759213 733785 Crisp2 cysteine-rich secretory protein 2 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20191114 MGI PMID:30759213 733785 Crisp2 cysteine-rich secretory protein 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20191114 MGI PMID:30759213 733785 Crisp2 cysteine-rich secretory protein 2 gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20191114 MGI PMID:30759213 733785 Crisp2 cysteine-rich secretory protein 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 733785 Crisp2 cysteine-rich secretory protein 2 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20240523 MGI 733785 Crisp2 cysteine-rich secretory protein 2 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20191114 MGI PMID:30759213 733786 Eaf2 ELL associated factor 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17873910 733786 Eaf2 ELL associated factor 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:17873910 733786 Eaf2 ELL associated factor 2 gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17873910 733786 Eaf2 ELL associated factor 2 gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17873910 733786 Eaf2 ELL associated factor 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17873910 733786 Eaf2 ELL associated factor 2 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17873910 733786 Eaf2 ELL associated factor 2 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17873910 733786 Eaf2 ELL associated factor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17873910 733786 Eaf2 ELL associated factor 2 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17873910 733786 Eaf2 ELL associated factor 2 gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20220303 MGI PMID:31229879 733786 Eaf2 ELL associated factor 2 gene MP:0003608 prostate gland inflammation IAGP N RGD:5509061 20210506 MGI PMID:31229879 733786 Eaf2 ELL associated factor 2 gene MP:0004961 increased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:17873910 733786 Eaf2 ELL associated factor 2 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:17873910 733786 Eaf2 ELL associated factor 2 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20210506 MGI PMID:31229879 733786 Eaf2 ELL associated factor 2 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17873910 733786 Eaf2 ELL associated factor 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17873910 733791 Ascl3 achaete-scute family bHLH transcription factor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18572159 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15143198 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:24209622 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:24209622 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15143198 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24209622 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15143198 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24209622 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24209622 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:15143198 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:15143198 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0004601 abnormal vertebral spinous process morphology IAGP N RGD:5509061 20141003 MGI PMID:15143198 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18719666 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15143198 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24209622 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24209622 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15143198 733792 Pip4k2b phosphatidylinositol-5-phosphate 4-kinase, type II, beta gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24209622 733795 St13 suppression of tumorigenicity 13 gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20240523 MGI PMID:35562743 733795 St13 suppression of tumorigenicity 13 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 733795 St13 suppression of tumorigenicity 13 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20240523 MGI PMID:35562743 733796 Fzd4 frizzled class receptor 4 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:15035989 733796 Fzd4 frizzled class receptor 4 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:15035989 733796 Fzd4 frizzled class receptor 4 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:16093361 733796 Fzd4 frizzled class receptor 4 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19837032 733796 Fzd4 frizzled class receptor 4 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0000467 abnormal esophagus morphology IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0000469 abnormal esophageal squamous epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:21343368 733796 Fzd4 frizzled class receptor 4 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:15035989 733796 Fzd4 frizzled class receptor 4 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:19837032 733796 Fzd4 frizzled class receptor 4 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0001133 impaired luteal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16093361 733796 Fzd4 frizzled class receptor 4 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:16093361 733796 Fzd4 frizzled class receptor 4 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:15035989 733796 Fzd4 frizzled class receptor 4 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:16093361 733796 Fzd4 frizzled class receptor 4 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 733796 Fzd4 frizzled class receptor 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15035989 733796 Fzd4 frizzled class receptor 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20230511 MGI PMID:33497368 733796 Fzd4 frizzled class receptor 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16093361 733796 Fzd4 frizzled class receptor 4 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16093361 733796 Fzd4 frizzled class receptor 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19837032 733796 Fzd4 frizzled class receptor 4 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:16093361 733796 Fzd4 frizzled class receptor 4 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15035989 733796 Fzd4 frizzled class receptor 4 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19837032 733796 Fzd4 frizzled class receptor 4 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:21343368 733796 Fzd4 frizzled class receptor 4 gene MP:0003356 impaired luteinization IAGP N RGD:5509061 20141003 MGI PMID:16093361 733796 Fzd4 frizzled class receptor 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19837032 733796 Fzd4 frizzled class receptor 4 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15035989 733796 Fzd4 frizzled class receptor 4 gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20141003 MGI PMID:15035989 733796 Fzd4 frizzled class receptor 4 gene MP:0004368 abnormal stria vascularis vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15035989 733796 Fzd4 frizzled class receptor 4 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15035989 733796 Fzd4 frizzled class receptor 4 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15035989 733796 Fzd4 frizzled class receptor 4 gene MP:0004545 enlarged esophagus IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:21343368 733796 Fzd4 frizzled class receptor 4 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19837032 733796 Fzd4 frizzled class receptor 4 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:16093361 733796 Fzd4 frizzled class receptor 4 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19837032 733796 Fzd4 frizzled class receptor 4 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:21743011 733796 Fzd4 frizzled class receptor 4 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20230511 MGI PMID:33497368 733796 Fzd4 frizzled class receptor 4 gene MP:0006185 retina hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15035989 733796 Fzd4 frizzled class receptor 4 gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:19837032 733796 Fzd4 frizzled class receptor 4 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:11425903 733796 Fzd4 frizzled class receptor 4 gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20141003 MGI PMID:19837032 733796 Fzd4 frizzled class receptor 4 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20230511 MGI PMID:33497368 733796 Fzd4 frizzled class receptor 4 gene MP:0009869 abnormal descending aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:19837032 733796 Fzd4 frizzled class receptor 4 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19837032 733796 Fzd4 frizzled class receptor 4 gene MP:0011111 lethality during fetal growth through weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21343368 733796 Fzd4 frizzled class receptor 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11425903 733799 Cblb Casitas B-lineage lymphoma b gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12415267 733799 Cblb Casitas B-lineage lymphoma b gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12415267 733799 Cblb Casitas B-lineage lymphoma b gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:12415267 733799 Cblb Casitas B-lineage lymphoma b gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12415267 733799 Cblb Casitas B-lineage lymphoma b gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12415267 733799 Cblb Casitas B-lineage lymphoma b gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:12415267 733799 Cblb Casitas B-lineage lymphoma b gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12415267 733799 Cblb Casitas B-lineage lymphoma b gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17868870 733799 Cblb Casitas B-lineage lymphoma b gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11070165 733799 Cblb Casitas B-lineage lymphoma b gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12415267 733799 Cblb Casitas B-lineage lymphoma b gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:14738763 733799 Cblb Casitas B-lineage lymphoma b gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:15589167 733799 Cblb Casitas B-lineage lymphoma b gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19009524 733799 Cblb Casitas B-lineage lymphoma b gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12415267 733799 Cblb Casitas B-lineage lymphoma b gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14738763 733799 Cblb Casitas B-lineage lymphoma b gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15589167 733799 Cblb Casitas B-lineage lymphoma b gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19009524 733799 Cblb Casitas B-lineage lymphoma b gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12415267 733799 Cblb Casitas B-lineage lymphoma b gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19009524 733799 Cblb Casitas B-lineage lymphoma b gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19009524 733799 Cblb Casitas B-lineage lymphoma b gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17868870 733799 Cblb Casitas B-lineage lymphoma b gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:15589167 733799 Cblb Casitas B-lineage lymphoma b gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:19009524 733799 Cblb Casitas B-lineage lymphoma b gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17868870 733800 Flot1 flotillin 1 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21059848 733800 Flot1 flotillin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20151217 MGI PMID:24465508 733800 Flot1 flotillin 1 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:21059848 733800 Flot1 flotillin 1 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:21059848 733800 Flot1 flotillin 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210520 MGI PMID:31138766 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20151231 MGI PMID:26542706 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16568086 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20151231 MGI PMID:26542706 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:10852963 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:12941696 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15607429 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:15607429 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:12941696 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20151231 MGI PMID:26542706 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20211021 MGI 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:12122119 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0001967 deafness IAGP N RGD:5509061 20231228 MGI PMID:26542706 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20151231 MGI PMID:26542706 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12941696 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0002750 exophthalmos IAGP N RGD:5509061 20151231 MGI PMID:26542706 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0003153 early eyelid opening IAGP N RGD:5509061 20151231 MGI PMID:26542706 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0003153 early eyelid opening IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12122119 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:16568086 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20151231 MGI PMID:26542706 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12122119 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20151231 MGI PMID:26542706 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20151231 MGI PMID:26542706 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20151231 MGI PMID:26542706 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:12122119 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:15795331 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20151231 MGI PMID:26542706 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:15795331 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12122119 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:12122119 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0009263 abnormal eyelid fusion IAGP N RGD:5509061 20150416 MGI PMID:12941696 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0009392 retina gliosis IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20141003 MGI PMID:10852963 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20141003 MGI PMID:15607429 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0009651 abnormal eyelid development IAGP N RGD:5509061 20150416 MGI PMID:12941696 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0009742 increased cornea stroma thickness IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12122119 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20200123 MGI PMID:21862560 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20141003 MGI 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16568086 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0011707 impaired fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:10852963 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20151231 MGI PMID:26542706 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20150108 MGI 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0013745 abnormal eyelid margin morphology IAGP N RGD:5509061 20150416 MGI PMID:12941696 733802 Map3k1 mitogen-activated protein kinase kinase kinase 1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20200123 MGI PMID:21862560 733805 Lst1 leukocyte specific transcript 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20170105 MGI 733805 Lst1 leukocyte specific transcript 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 733805 Lst1 leukocyte specific transcript 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20160811 MGI 733805 Lst1 leukocyte specific transcript 1 gene MP:0001147 small testis IEA N RGD:5509061 20160811 MGI 733805 Lst1 leukocyte specific transcript 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20231207 MGI 733805 Lst1 leukocyte specific transcript 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 733805 Lst1 leukocyte specific transcript 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20220811 MGI 733805 Lst1 leukocyte specific transcript 1 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:26817701 733805 Lst1 leukocyte specific transcript 1 gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:26817701 733807 Cdh17 cadherin 17 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15688343 733807 Cdh17 cadherin 17 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15688343 733807 Cdh17 cadherin 17 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15688343 733807 Cdh17 cadherin 17 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15688343 733807 Cdh17 cadherin 17 gene MP:0008168 decreased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:15688343 733807 Cdh17 cadherin 17 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:15688343 733807 Cdh17 cadherin 17 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:15688343 733807 Cdh17 cadherin 17 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15688343 733807 Cdh17 cadherin 17 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15688343 733807 Cdh17 cadherin 17 gene MP:0008484 decreased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:15688343 733807 Cdh17 cadherin 17 gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20190404 MGI 733808 Nab1 Ngfi-A binding protein 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:16136673 733808 Nab1 Ngfi-A binding protein 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16136673 733808 Nab1 Ngfi-A binding protein 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:16136673 733808 Nab1 Ngfi-A binding protein 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:16136673 733808 Nab1 Ngfi-A binding protein 1 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16136673 733808 Nab1 Ngfi-A binding protein 1 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:16136673 733808 Nab1 Ngfi-A binding protein 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16136673 733808 Nab1 Ngfi-A binding protein 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:16136673 733808 Nab1 Ngfi-A binding protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16136673 733808 Nab1 Ngfi-A binding protein 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16136673 733808 Nab1 Ngfi-A binding protein 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210826 MGI 733808 Nab1 Ngfi-A binding protein 1 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:16136673 733808 Nab1 Ngfi-A binding protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16136673 733808 Nab1 Ngfi-A binding protein 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210826 MGI 733808 Nab1 Ngfi-A binding protein 1 gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16136673 733808 Nab1 Ngfi-A binding protein 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16136673 733808 Nab1 Ngfi-A binding protein 1 gene MP:0011906 increased Schwann cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16136673 733808 Nab1 Ngfi-A binding protein 1 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:16136673 733812 Inhbc inhibin beta-C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10913194 733812 Inhbc inhibin beta-C gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20810712 733812 Inhbc inhibin beta-C gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:10913194 733813 Rab3il1 RAB3A interacting protein (rabin3)-like 1 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 733813 Rab3il1 RAB3A interacting protein (rabin3)-like 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20240523 MGI 733813 Rab3il1 RAB3A interacting protein (rabin3)-like 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20240523 MGI 733813 Rab3il1 RAB3A interacting protein (rabin3)-like 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 733813 Rab3il1 RAB3A interacting protein (rabin3)-like 1 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20240523 MGI 733813 Rab3il1 RAB3A interacting protein (rabin3)-like 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 733814 Bnip3 BCL2/adenovirus E1B interacting protein 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 733814 Bnip3 BCL2/adenovirus E1B interacting protein 3 gene MP:0001333 absent optic nerve IEA N RGD:5509061 20210520 MGI 733814 Bnip3 BCL2/adenovirus E1B interacting protein 3 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20201022 MGI 733814 Bnip3 BCL2/adenovirus E1B interacting protein 3 gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17909626 733814 Bnip3 BCL2/adenovirus E1B interacting protein 3 gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:17909626 733814 Bnip3 BCL2/adenovirus E1B interacting protein 3 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 733814 Bnip3 BCL2/adenovirus E1B interacting protein 3 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22021440 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:22267813 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0002418 increased susceptibility to viral infection IAGP N RGD:5509061 20210415 MGI PMID:29967452 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:16565719 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20210422 MGI PMID:26851218 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:22267813 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:16565719 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20210415 MGI PMID:29967452 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20210422 MGI PMID:26851218 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20210422 MGI PMID:26851218 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22267813 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22267813 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20180329 MGI PMID:29440507 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0009785 abnormal susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20180329 MGI PMID:29440507 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22267813 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20180329 MGI PMID:29440507 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20210415 MGI PMID:29967452 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20210422 MGI PMID:26851218 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0010839 decreased CD8-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22267813 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0013667 increased immature NK cell number IAGP N RGD:5509061 20210422 MGI PMID:26851218 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0013672 decreased mature NK cell number IAGP N RGD:5509061 20210422 MGI PMID:26851218 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:22267813 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0031025 decreased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:22267813 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:29440507 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0031045 decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:22267813 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0031045 decreased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:29440507 733815 Ncr1 natural cytotoxicity triggering receptor 1 gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:16565719 733817 Pdlim3 PDZ and LIM domain 3 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11329061 733817 Pdlim3 PDZ and LIM domain 3 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:11329061 733817 Pdlim3 PDZ and LIM domain 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11238905 733817 Pdlim3 PDZ and LIM domain 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:11329061 733817 Pdlim3 PDZ and LIM domain 3 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11329061 733817 Pdlim3 PDZ and LIM domain 3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:11329061 733817 Pdlim3 PDZ and LIM domain 3 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11329061 733817 Pdlim3 PDZ and LIM domain 3 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:11329061 733817 Pdlim3 PDZ and LIM domain 3 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11329061 733817 Pdlim3 PDZ and LIM domain 3 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:11329061 733817 Pdlim3 PDZ and LIM domain 3 gene MP:0010428 abnormal heart right ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:11329061 733817 Pdlim3 PDZ and LIM domain 3 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:11329061 733817 Pdlim3 PDZ and LIM domain 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11329061 733817 Pdlim3 PDZ and LIM domain 3 gene MP:0021160 decreased heart right ventricle wall thickness IAGP N RGD:5509061 20231221 MGI PMID:11329061 733817 Pdlim3 PDZ and LIM domain 3 gene MP:0031634 decreased heart right ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:11329061 733819 Mtnr1b melatonin receptor 1B gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20240229 MGI PMID:16203090 733819 Mtnr1b melatonin receptor 1B gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20240229 MGI PMID:16203090 733819 Mtnr1b melatonin receptor 1B gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12529409 733819 Mtnr1b melatonin receptor 1B gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 733819 Mtnr1b melatonin receptor 1B gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20240229 MGI PMID:16203090 733819 Mtnr1b melatonin receptor 1B gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:8614836 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:8614836 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:8878443 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9884344 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20170601 MGI PMID:27114035 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240905 MGI PMID:36715298 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16332958 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:20811150 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16332958 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:16332958 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:8614836 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:9541509 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:9884344 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0001860 liver inflammation IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0001861 lung inflammation IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20170601 MGI PMID:27114035 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:9884344 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20811150 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:16983074 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:9884344 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:16983074 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:9884344 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002833 increased heart weight IAGP N RGD:5509061 20170601 MGI PMID:27114035 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002833 increased heart weight IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002833 increased heart weight IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20240905 MGI PMID:36715298 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:9884344 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:20811150 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20170601 MGI PMID:27114035 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:8614836 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:9884344 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15001446 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16332958 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20811150 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:8878443 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:8614836 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:8614836 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003821 decreased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:8878443 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:8878443 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16332958 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0004070 abnormal P wave IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:16983074 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:15001446 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0004937 dilated heart IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16983074 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:8878443 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20240905 MGI PMID:36715298 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:8878443 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8878443 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:20811150 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:15001446 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9884344 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:8614836 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0005630 increased lung weight IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0006085 myocardium necrosis IAGP N RGD:5509061 20141003 MGI PMID:9884344 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0008775 abnormal heart ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:8614836 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0008775 abnormal heart ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:9541509 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20811150 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20811150 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0010534 calcified myocardium IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20170601 MGI PMID:27114035 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0010630 abnormal cardiac muscle tissue morphology IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0010632 cardiac muscle necrosis IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8614836 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9884344 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8878443 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20170831 MGI PMID:18362229 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20240905 MGI PMID:36715298 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20190905 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20240905 MGI PMID:36715298 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231221 MGI PMID:9884344 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:15001446 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:16332958 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:24829265 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:8614836 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:9884344 733823 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha gene MP:0031635 increased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:16332958 733824 Wap whey acidic protein gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20180719 MGI PMID:11494122 733824 Wap whey acidic protein gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20180719 MGI PMID:14661057 733824 Wap whey acidic protein gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20180719 MGI PMID:18443292 733824 Wap whey acidic protein gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20180719 MGI PMID:19174523 733824 Wap whey acidic protein gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:14661057 733824 Wap whey acidic protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:11494122 733824 Wap whey acidic protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:19208431 733824 Wap whey acidic protein gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20180719 MGI PMID:16106354 733824 Wap whey acidic protein gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20180719 MGI PMID:14661057 733824 Wap whey acidic protein gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20180719 MGI PMID:22034435 733824 Wap whey acidic protein gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20180719 MGI PMID:19174523 733824 Wap whey acidic protein gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20180719 MGI PMID:22034435 733824 Wap whey acidic protein gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:19174523 733827 Dcxr dicarbonyl L-xylulose reductase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 733827 Dcxr dicarbonyl L-xylulose reductase gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 733827 Dcxr dicarbonyl L-xylulose reductase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 733829 Sftpc surfactant associated protein C gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20180927 MGI PMID:29999500 733829 Sftpc surfactant associated protein C gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0001443 poor grooming IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0001958 emphysema IAGP N RGD:5509061 20180927 MGI PMID:29999500 733829 Sftpc surfactant associated protein C gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23285300 733829 Sftpc surfactant associated protein C gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22411819 733829 Sftpc surfactant associated protein C gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23285300 733829 Sftpc surfactant associated protein C gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22411819 733829 Sftpc surfactant associated protein C gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:22411819 733829 Sftpc surfactant associated protein C gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20180927 MGI PMID:29999500 733829 Sftpc surfactant associated protein C gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20141003 MGI PMID:11344267 733829 Sftpc surfactant associated protein C gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22411819 733829 Sftpc surfactant associated protein C gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:23285300 733829 Sftpc surfactant associated protein C gene MP:0010891 increased alveolar lamellar body number IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0010935 increased airway resistance IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0010943 abnormal bronchus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12519727 733829 Sftpc surfactant associated protein C gene MP:0010950 abnormal lung hysteresivity IAGP N RGD:5509061 20141003 MGI PMID:11344267 733829 Sftpc surfactant associated protein C gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:23285300 733830 Slc23a2 solute carrier family 23 (nucleobase transporters), member 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:11984597 733830 Slc23a2 solute carrier family 23 (nucleobase transporters), member 2 gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20141003 MGI PMID:12897061 733830 Slc23a2 solute carrier family 23 (nucleobase transporters), member 2 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:12897061 733830 Slc23a2 solute carrier family 23 (nucleobase transporters), member 2 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11984597 733830 Slc23a2 solute carrier family 23 (nucleobase transporters), member 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11984597 733830 Slc23a2 solute carrier family 23 (nucleobase transporters), member 2 gene MP:0002164 abnormal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:11984597 733830 Slc23a2 solute carrier family 23 (nucleobase transporters), member 2 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:12897061 733830 Slc23a2 solute carrier family 23 (nucleobase transporters), member 2 gene MP:0003834 abnormal adrenergic chromaffin cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12897061 733830 Slc23a2 solute carrier family 23 (nucleobase transporters), member 2 gene MP:0003962 abnormal adrenaline level IAGP N RGD:5509061 20141003 MGI PMID:12897061 733830 Slc23a2 solute carrier family 23 (nucleobase transporters), member 2 gene MP:0008291 abnormal adrenocortical cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12897061 733830 Slc23a2 solute carrier family 23 (nucleobase transporters), member 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11984597 733830 Slc23a2 solute carrier family 23 (nucleobase transporters), member 2 gene MP:0011229 abnormal vitamin C level IAGP N RGD:5509061 20141003 MGI PMID:11984597 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0000274 enlarged heart IAGP N RGD:5509061 20200430 MGI PMID:23648696 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0001265 decreased body size IAGP N RGD:5509061 20200430 MGI PMID:23648696 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:11461925 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:11461925 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200430 MGI PMID:23648696 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0001756 abnormal urination IAGP N RGD:5509061 20141003 MGI PMID:11461925 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:11461925 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0002893 ketoaciduria IAGP N RGD:5509061 20141003 MGI PMID:11461925 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200507 MGI PMID:31678161 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0003718 maternal effect IAGP N RGD:5509061 20200430 MGI PMID:23648696 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:11461925 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0003977 abnormal circulating carnitine level IAGP N RGD:5509061 20200430 MGI PMID:23648696 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20200507 MGI PMID:31678161 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:11461925 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20200507 MGI PMID:31678161 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20200430 MGI PMID:23648696 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200430 MGI PMID:23648696 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20200430 MGI PMID:23648696 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:11461925 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20200507 MGI PMID:31678161 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:11461925 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11461925 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:11461925 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0012557 decreased calcium uptake by cardiac muscle IAGP N RGD:5509061 20200507 MGI PMID:31678161 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0030655 increased circulating glycine level IAGP N RGD:5509061 20200430 MGI PMID:23648696 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0030673 increased circulating alanine level IAGP N RGD:5509061 20200430 MGI PMID:23648696 733831 Pcca propionyl-Coenzyme A carboxylase, alpha polypeptide gene MP:0030721 increased lysine level IAGP N RGD:5509061 20200430 MGI PMID:23648696 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15988029 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150716 MGI PMID:25843682 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19110448 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22101159 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0001874 acanthosis IAGP N RGD:5509061 20150716 MGI PMID:25843682 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20150716 MGI PMID:25843682 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0001926 female infertility IAGP N RGD:5509061 20150716 MGI PMID:25843682 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20170105 MGI 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19110448 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0002607 decreased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22101159 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20150716 MGI PMID:25843682 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17923505 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19110448 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0004947 skin inflammation IAGP N RGD:5509061 20150716 MGI PMID:25843682 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:19110448 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19110448 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:22101159 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19110448 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19110448 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0008758 abnormal T cell receptor beta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:19110448 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17923505 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20150716 MGI PMID:25843682 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0009583 increased keratinocyte proliferation IAGP N RGD:5509061 20150716 MGI PMID:25843682 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17923505 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17923505 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0011696 absent mast cells IAGP N RGD:5509061 20141003 MGI PMID:22101159 733834 Cpa3 carboxypeptidase A3, mast cell gene MP:0011696 absent mast cells IAGP N RGD:5509061 20150716 MGI PMID:25843682 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:16293761 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:16293761 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8701981 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:22198572 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22198572 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16293761 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22198572 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17680805 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141003 MGI PMID:22198572 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001283 sparse vibrissae IAGP N RGD:5509061 20141003 MGI PMID:22198572 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17680805 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22198572 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22198572 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20007321 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22198572 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17680805 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16293761 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:22198572 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001655 multifocal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:8701981 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:22198572 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0002263 abnormal laryngeal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22198572 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:8701981 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8701981 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15885355 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8467484 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:8701981 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:17680805 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:20007321 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0003742 narrow head IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:22198572 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:17680805 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8701981 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0004383 absent interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0004419 absent parietal bone IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0004443 absent supraoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0004557 dilated allantois IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22198572 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17239664 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:17680805 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:22198572 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15885355 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0008819 abnormal mastication IAGP N RGD:5509061 20141003 MGI PMID:16293761 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0008862 asymmetric snout IAGP N RGD:5509061 20141003 MGI PMID:16293761 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22198572 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0010043 abnormal frontonasal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0010166 increased response to stress-induced hyperthermia IAGP N RGD:5509061 20141003 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19109438 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0020427 increased hepatocyte karyomegaly IAGP N RGD:5509061 20170803 MGI PMID:8701981 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:22652393 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0030098 periorbital fullness IAGP N RGD:5509061 20170928 MGI PMID:16293761 733837 Gtf2ird1 general transcription factor II I repeat domain-containing 1 gene MP:0030098 periorbital fullness IAGP N RGD:5509061 20170928 MGI PMID:22652393 733840 Klk6 kallikrein related-peptidase 6 gene MP:0001230 epidermal desquamation IAGP N RGD:5509061 20200806 MGI PMID:31255470 733840 Klk6 kallikrein related-peptidase 6 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20200806 MGI PMID:31255470 733840 Klk6 kallikrein related-peptidase 6 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20200806 MGI PMID:30137206 733840 Klk6 kallikrein related-peptidase 6 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20200806 MGI PMID:31255470 733840 Klk6 kallikrein related-peptidase 6 gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20200806 MGI PMID:30137206 733840 Klk6 kallikrein related-peptidase 6 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20200806 MGI PMID:31255470 733840 Klk6 kallikrein related-peptidase 6 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20200806 MGI PMID:31255470 733840 Klk6 kallikrein related-peptidase 6 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20200806 MGI PMID:31255470 733840 Klk6 kallikrein related-peptidase 6 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23376368 733840 Klk6 kallikrein related-peptidase 6 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20200806 MGI PMID:30137206 733840 Klk6 kallikrein related-peptidase 6 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20200310 MGI PMID:23376368 733840 Klk6 kallikrein related-peptidase 6 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20200806 MGI PMID:30137206 733840 Klk6 kallikrein related-peptidase 6 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20200806 MGI PMID:30137206 733840 Klk6 kallikrein related-peptidase 6 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20200806 MGI PMID:31255470 733840 Klk6 kallikrein related-peptidase 6 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23376368 733840 Klk6 kallikrein related-peptidase 6 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:23376368 733840 Klk6 kallikrein related-peptidase 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200806 MGI PMID:31255470 733840 Klk6 kallikrein related-peptidase 6 gene MP:0012573 decreased susceptibility to chemically induced skin inflammation IAGP N RGD:5509061 20200806 MGI PMID:30137206 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:16141228 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:22484060 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:21559415 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:21559415 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:19144989 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:9109488 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:9109488 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9109488 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17194759 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:17194759 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16141228 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:9109488 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:9109488 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:21559415 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:9109488 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9109488 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19144989 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19144989 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17194759 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21559415 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23000963 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16141228 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16495313 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:9109488 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:21559415 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:12441287 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:16495313 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:10476967 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:22529374 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:12441287 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:21559415 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004132 absent embryonic cilia IAGP N RGD:5509061 20141003 MGI PMID:12441287 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12441287 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:12441287 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:21559415 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004330 abnormal vestibular saccular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:16495313 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:16495313 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16141228 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16495313 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16141228 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16495313 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004497 decreased organ of Corti supporting cell number IAGP N RGD:5509061 20141003 MGI PMID:16141228 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16141228 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004647 decreased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:17194759 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:19144989 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:20081190 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:20081190 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0005567 decreased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0006135 artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:19144989 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9109488 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0008137 absent podocytes IAGP N RGD:5509061 20141003 MGI PMID:23806616 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:15146182 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0008822 decreased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:20081190 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:20081190 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:9109488 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0010119 abnormal bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20220915 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0010463 aorta stenosis IAGP N RGD:5509061 20141003 MGI PMID:19144989 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0010515 abnormal Q wave IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17194759 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20081190 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9109488 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:23806616 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20190725 MGI PMID:17194759 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0012024 abnormal nephron morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:23806616 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0012675 enlarged floor plate IAGP N RGD:5509061 20141003 MGI PMID:12441287 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0012728 abnormal somite border morphology IAGP N RGD:5509061 20141003 MGI PMID:9109488 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0014273 abnormal skin vasculature morphology IAGP N RGD:5509061 20230810 MGI PMID:19144989 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20160421 MGI PMID:19562077 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0020327 abnormal capillary branching pattern IAGP N RGD:5509061 20230810 MGI PMID:19144989 733843 Dll1 delta like canonical Notch ligand 1 gene MP:0030958 abnormal myotube differentiation IAGP N RGD:5509061 20190725 MGI PMID:17194759 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11907043 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11907043 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11907043 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200514 MGI 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11907043 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11507092 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0001925 male infertility IAGP N RGD:5509061 20230223 MGI PMID:35228556 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11507092 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11507092 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11507092 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230223 MGI PMID:35228556 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:11907043 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20220519 MGI 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230223 MGI PMID:35228556 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20230223 MGI PMID:35228556 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20230223 MGI PMID:35228556 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20230223 MGI PMID:35228556 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20141003 MGI PMID:11507092 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:11507092 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11907043 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0014344 abnormal skeletal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:11507092 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0014464 decreased sperm mitochondrial sheath size IAGP N RGD:5509061 20240613 MGI PMID:35228556 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:11507092 733845 Vdac3 voltage-dependent anion channel 3 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220714 MGI PMID:11507092 733847 Ppm1b protein phosphatase 1B, magnesium dependent, beta isoform gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20180208 MGI PMID:25751141 733847 Ppm1b protein phosphatase 1B, magnesium dependent, beta isoform gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17499977 733847 Ppm1b protein phosphatase 1B, magnesium dependent, beta isoform gene MP:0010769 abnormal survival IAGP N RGD:5509061 20180208 MGI PMID:25751141 733847 Ppm1b protein phosphatase 1B, magnesium dependent, beta isoform gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17499977 733850 Lhx2 LIM homeobox protein 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:20386748 733850 Lhx2 LIM homeobox protein 2 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:20386748 733850 Lhx2 LIM homeobox protein 2 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19820705 733850 Lhx2 LIM homeobox protein 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:19820705 733850 Lhx2 LIM homeobox protein 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18202285 733850 Lhx2 LIM homeobox protein 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17350283 733850 Lhx2 LIM homeobox protein 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:19820705 733850 Lhx2 LIM homeobox protein 2 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:18202285 733850 Lhx2 LIM homeobox protein 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:20386748 733850 Lhx2 LIM homeobox protein 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:21886788 733850 Lhx2 LIM homeobox protein 2 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20386748 733850 Lhx2 LIM homeobox protein 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:20386748 733850 Lhx2 LIM homeobox protein 2 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:21886788 733850 Lhx2 LIM homeobox protein 2 gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0005267 abnormal olfactory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19820705 733850 Lhx2 LIM homeobox protein 2 gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17350283 733850 Lhx2 LIM homeobox protein 2 gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19820705 733850 Lhx2 LIM homeobox protein 2 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20141003 MGI PMID:20386748 733850 Lhx2 LIM homeobox protein 2 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0009773 absent retina IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0012170 absent optic placodes IAGP N RGD:5509061 20141003 MGI PMID:9247336 733850 Lhx2 LIM homeobox protein 2 gene MP:0021092 abnormal dorsal interneuron 1 morphology IAGP N RGD:5509061 20220310 MGI PMID:18701067 733850 Lhx2 LIM homeobox protein 2 gene MP:0030047 flat forehead IAGP N RGD:5509061 20170921 MGI PMID:9247336 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0000023 abnormal ear position IEA N RGD:5509061 20150521 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0000026 abnormal inner ear morphology IEA N RGD:5509061 20111116 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:8790740 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:21689626 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:8790740 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:14759567 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:19270079 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:21689626 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20170216 MGI PMID:22326520 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0000048 abnormal stria vascularis morphology IEA N RGD:5509061 20150521 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210128 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20181227 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:5955164 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001262 decreased body weight IEA N RGD:5509061 20190103 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001386 abnormal maternal nurturing IEA N RGD:5509061 20111116 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:5955164 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:5955164 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11750125 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10452381 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11322776 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:16235133 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:5955164 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:9021139 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:9021139 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:5955164 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001408 stereotypic behavior IEA N RGD:5509061 20181227 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001410 head bobbing IEA N RGD:5509061 20111116 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:5955164 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20141003 MGI PMID:8790740 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17329413 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001512 trunk curl IEA N RGD:5509061 20181227 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:13336002 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:16235133 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001523 impaired righting response IEA N RGD:5509061 20181227 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9021139 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:16235133 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:19270079 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11322776 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:13336002 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15820310 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:19270079 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:20644563 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:5955164 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:9021139 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:9325047 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0001967 deafness IAGP N RGD:5509061 20170216 MGI PMID:22326520 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20150521 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11138008 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16281288 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19270079 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8790740 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:11322776 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:5955164 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:5955164 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21689626 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8790740 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:13336002 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:15537665 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:19270079 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0002894 abnormal otolith morphology IEA N RGD:5509061 20111116 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20181227 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:5955164 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9133426 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0003637 cochlear ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14759567 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:5955164 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0003878 abnormal ear physiology IAGP N RGD:5509061 20141003 MGI PMID:11138008 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004329 vestibular saccular degeneration IEA N RGD:5509061 20111116 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004331 vestibular saccular macula degeneration IAGP N RGD:5509061 20141003 MGI PMID:13336002 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:13336002 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15537665 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19270079 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21689626 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20170216 MGI PMID:22326520 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20170615 MGI PMID:28287619 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004363 stria vascularis degeneration IEA N RGD:5509061 20111116 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:14648237 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:20644563 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20170608 MGI PMID:28287619 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20170216 MGI PMID:22326520 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20170615 MGI PMID:28287619 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11138008 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11322776 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20332152 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:14648237 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:20644563 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20170608 MGI PMID:28287619 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21689626 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20170216 MGI PMID:22326520 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20170615 MGI PMID:28287619 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004408 decreased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:9133426 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004408 decreased cochlear hair cell number IAGP N RGD:5509061 20170608 MGI PMID:28287619 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004413 absent cochlear microphonics IAGP N RGD:5509061 20141003 MGI PMID:21436032 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004415 abnormal cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:14648237 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20141003 MGI PMID:21436032 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004432 abnormal cochlear hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19270079 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004432 abnormal cochlear hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22787034 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20644563 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:8790740 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:8790740 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:11138008 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20170216 MGI PMID:22326520 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:18339676 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004523 decreased cochlear hair cell stereocilia number IAGP N RGD:5509061 20170216 MGI PMID:22326520 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:11138008 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:11322776 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:12121736 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:14648237 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15537665 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:20332152 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:21436032 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:8790740 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20170216 MGI PMID:22326520 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:11138008 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:14648237 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:21436032 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004530 absent outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:11138008 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004531 short outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:21436032 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:11138008 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:12121736 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15537665 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:21436032 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:21689626 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:8790740 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:21436032 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004536 short inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:21436032 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004577 abnormal cochlear hair cell inter-stereocilial links morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004578 abnormal cochlear hair bundle tip links morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004578 abnormal cochlear hair bundle tip links morphology IAGP N RGD:5509061 20141003 MGI PMID:19270079 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004578 abnormal cochlear hair bundle tip links morphology IAGP N RGD:5509061 20141003 MGI PMID:21436032 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004578 abnormal cochlear hair bundle tip links morphology IAGP N RGD:5509061 20170216 MGI PMID:22326520 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004597 increased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20141003 MGI PMID:14648237 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:17360538 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:20644563 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20170216 MGI PMID:22326520 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:19270079 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:20644563 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:21436032 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20644563 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11750125 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:11175788 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12121736 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12910270 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:14648237 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:15537665 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:15820310 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:18662770 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:9325047 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:10452381 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:10452381 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:9021139 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0005357 novel environmental response-related retropulsion IEA N RGD:5509061 20111116 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:14609561 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20181227 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20181227 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:14648237 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:19270079 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:20644563 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:21436032 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:21689626 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0006335 abnormal hearing electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21436032 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:11322776 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:12121736 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:20644563 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0006359 absent startle reflex IAGP N RGD:5509061 20141003 MGI PMID:8790740 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20181227 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011061 abnormal inner hair cell kinocilium morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011062 abnormal outer hair cell kinocilium morphology IAGP N RGD:5509061 20141003 MGI PMID:18339676 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11138008 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11175788 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11750125 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15537665 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17329413 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18662770 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:19270079 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21436032 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21689626 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:22381527 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:9325047 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20170216 MGI PMID:22326520 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20170608 MGI PMID:28287619 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0012148 decreased a-wave implicit time IAGP N RGD:5509061 20141003 MGI PMID:14609561 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0012149 decreased b-wave implicit time IAGP N RGD:5509061 20141003 MGI PMID:14609561 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 733852 Cdh23 cadherin related 23 (otocadherin) gene MP:0030961 abnormal outer hair cell kinocilium location or orientation IAGP N RGD:5509061 20190725 MGI PMID:11138008 733854 Ifit1 interferon-induced protein with tetratricopeptide repeats 1 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20200709 MGI PMID:24198415 733854 Ifit1 interferon-induced protein with tetratricopeptide repeats 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20200709 MGI PMID:24198415 733854 Ifit1 interferon-induced protein with tetratricopeptide repeats 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20200709 MGI PMID:24198415 733854 Ifit1 interferon-induced protein with tetratricopeptide repeats 1 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20200709 MGI PMID:24198415 733854 Ifit1 interferon-induced protein with tetratricopeptide repeats 1 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:21642987 733854 Ifit1 interferon-induced protein with tetratricopeptide repeats 1 gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200709 MGI PMID:24198415 733854 Ifit1 interferon-induced protein with tetratricopeptide repeats 1 gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:21642987 733854 Ifit1 interferon-induced protein with tetratricopeptide repeats 1 gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200709 MGI PMID:24198415 733857 Polr2g polymerase (RNA) II (DNA directed) polypeptide G gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 733857 Polr2g polymerase (RNA) II (DNA directed) polypeptide G gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 733863 Cdc123 cell division cycle 123 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20160421 MGI 733863 Cdc123 cell division cycle 123 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20170105 MGI 733863 Cdc123 cell division cycle 123 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20211021 MGI 733863 Cdc123 cell division cycle 123 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733866 Dnase1l3 deoxyribonuclease 1-like 3 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:24312463 733866 Dnase1l3 deoxyribonuclease 1-like 3 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 733866 Dnase1l3 deoxyribonuclease 1-like 3 gene MP:0000601 small liver IEA N RGD:5509061 20230119 MGI 733866 Dnase1l3 deoxyribonuclease 1-like 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 733866 Dnase1l3 deoxyribonuclease 1-like 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 733866 Dnase1l3 deoxyribonuclease 1-like 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 733866 Dnase1l3 deoxyribonuclease 1-like 3 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230119 MGI 733866 Dnase1l3 deoxyribonuclease 1-like 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230119 MGI 733866 Dnase1l3 deoxyribonuclease 1-like 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230119 MGI 733866 Dnase1l3 deoxyribonuclease 1-like 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230119 MGI 733866 Dnase1l3 deoxyribonuclease 1-like 3 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20231207 MGI 733866 Dnase1l3 deoxyribonuclease 1-like 3 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20231207 MGI 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:23362348 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:19830824 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:7990960 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:19830824 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:20371632 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0000528 delayed kidney development IAGP N RGD:5509061 20141003 MGI PMID:7990960 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11920562 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19285468 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19285468 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:9989404 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:20371632 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20371632 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:24036309 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:9989404 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:20371632 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:9989404 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20371632 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:19285468 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:23362348 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19830824 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20371632 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:9989404 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:20371632 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23362348 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0002909 abnormal adrenal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:12399432 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:19830824 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0002989 small kidney IAGP N RGD:5509061 20150205 MGI PMID:24904088 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:19830824 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0003582 abnormal ovary development IAGP N RGD:5509061 20141003 MGI PMID:19830824 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0003582 abnormal ovary development IAGP N RGD:5509061 20141003 MGI PMID:20371632 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:7990960 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20141003 MGI PMID:20371632 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9620855 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:15930111 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:20371632 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0004755 abnormal loop of Henle morphology IAGP N RGD:5509061 20141003 MGI PMID:23362348 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:23362348 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:20371632 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20150205 MGI PMID:24904088 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20150205 MGI PMID:24904088 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:24036309 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:9989404 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0006361 abnormal female germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9989404 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0006425 absent Mullerian ducts IAGP N RGD:5509061 20141003 MGI PMID:9989404 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0008329 decreased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9620855 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0008335 decreased gonadotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9620855 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0008338 decreased thyrotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:9620855 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:9989404 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:37000005 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:37000005 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:37000005 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20201015 MGI PMID:32497039 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20201015 MGI PMID:32497039 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:7990960 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0010985 abnormal kidney mesenchyme morphology IAGP N RGD:5509061 20141204 MGI PMID:19830824 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0010987 abnormal nephrogenic mesenchyme morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:7990960 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20371632 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23362348 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21490063 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7990960 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19285468 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20231109 MGI PMID:37000005 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0011364 abnormal metanephros morphology IAGP N RGD:5509061 20141003 MGI PMID:23362348 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0011365 small metanephros IAGP N RGD:5509061 20141003 MGI PMID:15930111 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0011682 renal glomerulus cyst IAGP N RGD:5509061 20141003 MGI PMID:23362348 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0013312 absent ovary capsule IAGP N RGD:5509061 20141204 MGI PMID:19830824 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0013618 decreased areal bone mineral density IAGP N RGD:5509061 20201015 MGI PMID:32497039 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20201015 MGI PMID:32497039 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0021182 decreased femoral compact bone area IAGP N RGD:5509061 20220915 MGI PMID:32497039 733868 Wnt4 wingless-type MMTV integration site family, member 4 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20240125 MGI PMID:37000005 733871 Gucy2e guanylate cyclase 2e gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17255100 733871 Gucy2e guanylate cyclase 2e gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17255100 733871 Gucy2e guanylate cyclase 2e gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:17255100 733871 Gucy2e guanylate cyclase 2e gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10407028 733871 Gucy2e guanylate cyclase 2e gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17255100 733871 Gucy2e guanylate cyclase 2e gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10407028 733871 Gucy2e guanylate cyclase 2e gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:17255100 733871 Gucy2e guanylate cyclase 2e gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10407028 733871 Gucy2e guanylate cyclase 2e gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17255100 733871 Gucy2e guanylate cyclase 2e gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20180201 MGI PMID:26247368 733871 Gucy2e guanylate cyclase 2e gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10407028 733871 Gucy2e guanylate cyclase 2e gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17255100 733871 Gucy2e guanylate cyclase 2e gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20180201 MGI PMID:26247368 733871 Gucy2e guanylate cyclase 2e gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:10407028 733871 Gucy2e guanylate cyclase 2e gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:17255100 733871 Gucy2e guanylate cyclase 2e gene MP:0008448 abnormal retina cone cell inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:17255100 733871 Gucy2e guanylate cyclase 2e gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:17255100 733871 Gucy2e guanylate cyclase 2e gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:17255100 733871 Gucy2e guanylate cyclase 2e gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20180201 MGI PMID:26247368 733871 Gucy2e guanylate cyclase 2e gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:17255100 733871 Gucy2e guanylate cyclase 2e gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20180201 MGI PMID:26247368 733871 Gucy2e guanylate cyclase 2e gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20180201 MGI PMID:26247368 733871 Gucy2e guanylate cyclase 2e gene MP:0012671 retina spots IEA N RGD:5509061 20190207 MGI 733871 Gucy2e guanylate cyclase 2e gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:17255100 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20220519 MGI 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20181101 MGI PMID:25851903 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20181101 MGI PMID:25851903 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20181101 MGI PMID:25851903 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0003718 maternal effect IAGP N RGD:5509061 20181101 MGI PMID:25851903 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20181101 MGI PMID:25851903 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20181101 MGI PMID:25851903 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20181101 MGI PMID:25851903 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0009615 abnormal zinc homeostasis IAGP N RGD:5509061 20181101 MGI PMID:25851903 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0010173 increased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20181101 MGI PMID:25851903 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20181101 MGI PMID:25851903 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0013716 hypolactation IAGP N RGD:5509061 20181101 MGI PMID:25851903 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0013781 abnormal mammary gland luminal epithelium morphology IAGP N RGD:5509061 20181101 MGI PMID:25851903 733875 Slc30a2 solute carrier family 30 (zinc transporter), member 2 gene MP:0014126 increased mammary gland apoptosis IAGP N RGD:5509061 20181101 MGI PMID:25851903 733879 Klc3 kinesin light chain 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240307 MGI PMID:37776549 733879 Klc3 kinesin light chain 3 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 733881 Cdk12 cyclin dependent kinase 12 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 733881 Cdk12 cyclin dependent kinase 12 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20210128 MGI 733881 Cdk12 cyclin dependent kinase 12 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20220519 MGI 733881 Cdk12 cyclin dependent kinase 12 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 733881 Cdk12 cyclin dependent kinase 12 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20231207 MGI 733881 Cdk12 cyclin dependent kinase 12 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20220519 MGI 733881 Cdk12 cyclin dependent kinase 12 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210520 MGI 733881 Cdk12 cyclin dependent kinase 12 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20170824 MGI PMID:26658019 733881 Cdk12 cyclin dependent kinase 12 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 733881 Cdk12 cyclin dependent kinase 12 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210128 MGI 733881 Cdk12 cyclin dependent kinase 12 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 733881 Cdk12 cyclin dependent kinase 12 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 733881 Cdk12 cyclin dependent kinase 12 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20170824 MGI PMID:26658019 733881 Cdk12 cyclin dependent kinase 12 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20170824 MGI PMID:26658019 733881 Cdk12 cyclin dependent kinase 12 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20170824 MGI PMID:26658019 733881 Cdk12 cyclin dependent kinase 12 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 733881 Cdk12 cyclin dependent kinase 12 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20170824 MGI PMID:26658019 733881 Cdk12 cyclin dependent kinase 12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20181227 MGI 733881 Cdk12 cyclin dependent kinase 12 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 733881 Cdk12 cyclin dependent kinase 12 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 733885 Amph amphiphysin gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11879655 733885 Amph amphiphysin gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11879655 733885 Amph amphiphysin gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11879655 733885 Amph amphiphysin gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17785912 733885 Amph amphiphysin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11879655 733885 Amph amphiphysin gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17785912 733885 Amph amphiphysin gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:11879655 733885 Amph amphiphysin gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:11879655 733885 Amph amphiphysin gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20141003 MGI PMID:17785912 733885 Amph amphiphysin gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:11879655 733885 Amph amphiphysin gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17785912 733886 Fmod fibromodulin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20151217 MGI PMID:16612079 733886 Fmod fibromodulin gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11978731 733886 Fmod fibromodulin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:12766039 733886 Fmod fibromodulin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11978731 733886 Fmod fibromodulin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0002697 abnormal eye size IAGP N RGD:5509061 20141003 MGI PMID:12766039 733886 Fmod fibromodulin gene MP:0002698 abnormal sclera morphology IAGP N RGD:5509061 20141003 MGI PMID:12766039 733886 Fmod fibromodulin gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:11978731 733886 Fmod fibromodulin gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0003098 decreased tendon stiffness IAGP N RGD:5509061 20141003 MGI PMID:11978731 733886 Fmod fibromodulin gene MP:0003098 decreased tendon stiffness IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0003098 decreased tendon stiffness IAGP N RGD:5509061 20141003 MGI PMID:12766039 733886 Fmod fibromodulin gene MP:0003099 retina detachment IAGP N RGD:5509061 20141003 MGI PMID:12766039 733886 Fmod fibromodulin gene MP:0003101 high myopia IAGP N RGD:5509061 20141003 MGI PMID:12766039 733886 Fmod fibromodulin gene MP:0003102 sclera thinning IAGP N RGD:5509061 20141003 MGI PMID:12766039 733886 Fmod fibromodulin gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:11978731 733886 Fmod fibromodulin gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0005353 abnormal patella morphology IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:10092650 733886 Fmod fibromodulin gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:11076963 733886 Fmod fibromodulin gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:11978731 733886 Fmod fibromodulin gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20151217 MGI PMID:16612079 733886 Fmod fibromodulin gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20151217 MGI PMID:16006154 733886 Fmod fibromodulin gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11978731 733886 Fmod fibromodulin gene MP:0009275 bruising IAGP N RGD:5509061 20141003 MGI PMID:12089156 733886 Fmod fibromodulin gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:11978731 733886 Fmod fibromodulin gene MP:0013304 osteophytes IAGP N RGD:5509061 20151217 MGI PMID:16006154 733886 Fmod fibromodulin gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171109 MGI PMID:16006154 733886 Fmod fibromodulin gene MP:0030332 accelerated temporomandibular joint osteoarthritis IAGP N RGD:5509061 20171109 MGI PMID:16006154 733886 Fmod fibromodulin gene MP:0030332 accelerated temporomandibular joint osteoarthritis IAGP N RGD:5509061 20171109 MGI PMID:16612079 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11500373 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:11500373 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11500373 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0001062 absent oculomotor nerve IAGP N RGD:5509061 20141003 MGI PMID:11500373 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0001064 absent trochlear nerve IAGP N RGD:5509061 20141003 MGI PMID:11500373 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11500373 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:18579678 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11500373 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11500373 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:11500373 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:15496443 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0003661 abnormal locus ceruleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11500373 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11500373 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18579678 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0004280 abnormal oculomotor nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11500373 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:18579678 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0008949 increased Cajal-Retzius cell number IAGP N RGD:5509061 20141003 MGI PMID:18579678 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18579678 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11500373 733887 Hes3 hes family bHLH transcription factor 3 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:11500373 733890 Cd14 CD14 antigen gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15208271 733890 Cd14 CD14 antigen gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11145687 733890 Cd14 CD14 antigen gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8612135 733890 Cd14 CD14 antigen gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16148141 733890 Cd14 CD14 antigen gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:11145687 733890 Cd14 CD14 antigen gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11035061 733890 Cd14 CD14 antigen gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:15731076 733890 Cd14 CD14 antigen gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:15208271 733890 Cd14 CD14 antigen gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:15208271 733890 Cd14 CD14 antigen gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:8612135 733890 Cd14 CD14 antigen gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20141003 MGI PMID:15895089 733890 Cd14 CD14 antigen gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:11035061 733890 Cd14 CD14 antigen gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:15895089 733890 Cd14 CD14 antigen gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16148141 733890 Cd14 CD14 antigen gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:8612135 733890 Cd14 CD14 antigen gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:8612135 733890 Cd14 CD14 antigen gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:11035061 733890 Cd14 CD14 antigen gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:8612135 733890 Cd14 CD14 antigen gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:15731076 733890 Cd14 CD14 antigen gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:15895089 733890 Cd14 CD14 antigen gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:8612135 733890 Cd14 CD14 antigen gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:15731076 733890 Cd14 CD14 antigen gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15731076 733890 Cd14 CD14 antigen gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16204620 733890 Cd14 CD14 antigen gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:8612135 733890 Cd14 CD14 antigen gene MP:0009878 decreased susceptibility to bone fracture IAGP N RGD:5509061 20141003 MGI PMID:15208271 733890 Cd14 CD14 antigen gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15208271 733890 Cd14 CD14 antigen gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:15208271 733890 Cd14 CD14 antigen gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:15895089 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17293880 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0000084 abnormal fontanelle morphology IAGP N RGD:5509061 20141003 MGI PMID:17786208 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:23185619 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18288891 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20818428 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:10894547 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10894547 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:18212115 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20357757 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20357757 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20220421 MGI PMID:20357757 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:15282284 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18958152 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:17786208 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18288891 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:20357757 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:20357757 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:18958152 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18288891 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18288891 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:24099767 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:15282284 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:20680007 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18288891 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:20357757 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20141003 MGI PMID:24099767 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:21737790 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:21737790 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0003064 decreased coping response IAGP N RGD:5509061 20141003 MGI PMID:20357757 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20210204 MGI PMID:27170944 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20210204 MGI PMID:27170944 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:17786208 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:17293880 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0004679 xiphoid process foramen IAGP N RGD:5509061 20141003 MGI PMID:17293880 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:20680007 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:17786208 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:17786208 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20210204 MGI PMID:27170944 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18288891 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17786208 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:18288891 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15791206 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21035757 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0005440 increased glycogen level IAGP N RGD:5509061 20141003 MGI PMID:20680007 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18288891 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18288891 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:17786208 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:17293880 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:18958152 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20357757 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:18288891 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:20592205 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20210819 MGI PMID:20357757 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20210819 MGI PMID:20357757 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0009488 abnormal pancreatic islet cell apoptosis IAGP N RGD:5509061 20180614 MGI PMID:18288891 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20141003 MGI PMID:20981831 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20357757 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20220721 MGI PMID:20981831 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:17293880 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:20981831 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:17293880 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:20981831 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20210204 MGI PMID:27170944 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:15791206 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20210204 MGI PMID:27170944 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0010509 decreased P wave amplitude IAGP N RGD:5509061 20210204 MGI PMID:27170944 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0010631 increased Q wave amplitude IAGP N RGD:5509061 20210204 MGI PMID:27170944 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0010653 abnormal Wallerian degeneration IAGP N RGD:5509061 20141003 MGI PMID:23015435 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:17786208 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:17786208 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:24099767 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0010961 increased compact bone mass IAGP N RGD:5509061 20141003 MGI PMID:17786208 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0010964 increased compact bone volume IAGP N RGD:5509061 20141003 MGI PMID:24099767 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17293880 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20981831 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10894547 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:17786208 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20180614 MGI PMID:18288891 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0011920 abnormal S wave IAGP N RGD:5509061 20210204 MGI PMID:27170944 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:17786208 733892 Gsk3b glycogen synthase kinase 3 beta gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:20981831 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0000274 enlarged heart IAGP N RGD:5509061 20200206 MGI PMID:31209364 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20200206 MGI PMID:31209364 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23466696 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23466696 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:23466696 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20200206 MGI PMID:31209364 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0001577 anemia IAGP N RGD:5509061 20200206 MGI PMID:31601784 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20200206 MGI PMID:31601784 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20393889 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0002083 premature death IAGP N RGD:5509061 20200206 MGI PMID:31209364 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20200206 MGI PMID:31209364 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20200206 MGI PMID:31601784 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:23466696 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200206 MGI PMID:31209364 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20141003 MGI PMID:23466696 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20200206 MGI PMID:31601784 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0003674 oxidative stress IAGP N RGD:5509061 20200206 MGI PMID:31209364 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20393889 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200206 MGI PMID:31601784 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:20393889 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0005630 increased lung weight IAGP N RGD:5509061 20200206 MGI PMID:31209364 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:23466696 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20200206 MGI PMID:31209364 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20200206 MGI PMID:31209364 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20200206 MGI PMID:31209364 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:23466696 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:23466696 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20393889 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200206 MGI PMID:31601784 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20393889 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20141003 MGI PMID:23466696 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20200206 MGI PMID:31209364 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0012051 spasticity IAGP N RGD:5509061 20141003 MGI PMID:23466696 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0012688 abnormal heart ventricles weight IAGP N RGD:5509061 20200206 MGI PMID:31209364 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0013657 abnormal blood cell morphology IAGP N RGD:5509061 20200206 MGI PMID:31601784 733896 Hspd1 heat shock protein 1 (chaperonin) gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:31209364 733900 Rad50 RAD50 double strand break repair protein gene MP:0000175 absent bone marrow cell IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19001091 733900 Rad50 RAD50 double strand break repair protein gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10377422 733900 Rad50 RAD50 double strand break repair protein gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19001091 733900 Rad50 RAD50 double strand break repair protein gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19001091 733900 Rad50 RAD50 double strand break repair protein gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0001147 small testis IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19001091 733900 Rad50 RAD50 double strand break repair protein gene MP:0001545 abnormal hematopoietic system physiology IAGP N RGD:5509061 20141003 MGI PMID:16357220 733900 Rad50 RAD50 double strand break repair protein gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16357220 733900 Rad50 RAD50 double strand break repair protein gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17429352 733900 Rad50 RAD50 double strand break repair protein gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10377422 733900 Rad50 RAD50 double strand break repair protein gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10377422 733900 Rad50 RAD50 double strand break repair protein gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:20483988 733900 Rad50 RAD50 double strand break repair protein gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0001925 male infertility IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0001926 female infertility IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0001935 decreased litter size IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:10377422 733900 Rad50 RAD50 double strand break repair protein gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16357220 733900 Rad50 RAD50 double strand break repair protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17429352 733900 Rad50 RAD50 double strand break repair protein gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:10377422 733900 Rad50 RAD50 double strand break repair protein gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0002328 abnormal airway resistance IAGP N RGD:5509061 20141003 MGI PMID:20483988 733900 Rad50 RAD50 double strand break repair protein gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:20483988 733900 Rad50 RAD50 double strand break repair protein gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16357220 733900 Rad50 RAD50 double strand break repair protein gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16357220 733900 Rad50 RAD50 double strand break repair protein gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20483988 733900 Rad50 RAD50 double strand break repair protein gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:20483988 733900 Rad50 RAD50 double strand break repair protein gene MP:0002673 abnormal sperm number IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0003134 increased late pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:16357220 733900 Rad50 RAD50 double strand break repair protein gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16357220 733900 Rad50 RAD50 double strand break repair protein gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19001091 733900 Rad50 RAD50 double strand break repair protein gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:16357220 733900 Rad50 RAD50 double strand break repair protein gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:16357220 733900 Rad50 RAD50 double strand break repair protein gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:16357220 733900 Rad50 RAD50 double strand break repair protein gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0004849 abnormal testis size IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:16357220 733900 Rad50 RAD50 double strand break repair protein gene MP:0005152 pancytopenia IAGP N RGD:5509061 20141003 MGI PMID:16357220 733900 Rad50 RAD50 double strand break repair protein gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0005432 abnormal pro-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16357220 733900 Rad50 RAD50 double strand break repair protein gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:20483988 733900 Rad50 RAD50 double strand break repair protein gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:15608641 733900 Rad50 RAD50 double strand break repair protein gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:20483988 733900 Rad50 RAD50 double strand break repair protein gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17429352 733900 Rad50 RAD50 double strand break repair protein gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16357220 733900 Rad50 RAD50 double strand break repair protein gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20483988 733900 Rad50 RAD50 double strand break repair protein gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:23569250 733900 Rad50 RAD50 double strand break repair protein gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:15608641 733900 Rad50 RAD50 double strand break repair protein gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:20483988 733900 Rad50 RAD50 double strand break repair protein gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:23569250 733900 Rad50 RAD50 double strand break repair protein gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:23569250 733900 Rad50 RAD50 double strand break repair protein gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15608641 733900 Rad50 RAD50 double strand break repair protein gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20483988 733900 Rad50 RAD50 double strand break repair protein gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:23569250 733900 Rad50 RAD50 double strand break repair protein gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:23569250 733900 Rad50 RAD50 double strand break repair protein gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:15608641 733900 Rad50 RAD50 double strand break repair protein gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:20483988 733900 Rad50 RAD50 double strand break repair protein gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:23569250 733900 Rad50 RAD50 double strand break repair protein gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:20483988 733900 Rad50 RAD50 double strand break repair protein gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0010054 increased hepatoblastoma incidence IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20483988 733900 Rad50 RAD50 double strand break repair protein gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10377422 733900 Rad50 RAD50 double strand break repair protein gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12208847 733900 Rad50 RAD50 double strand break repair protein gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20150212 MGI PMID:24532689 733900 Rad50 RAD50 double strand break repair protein gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16357220 733900 Rad50 RAD50 double strand break repair protein gene MP:0030926 increased skin pigmentation IAGP N RGD:5509061 20190117 MGI PMID:24532689 733901 Tacr2 tachykinin receptor 2 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20210415 MGI PMID:33427049 733901 Tacr2 tachykinin receptor 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20210415 MGI PMID:33427049 733904 Stc2 stanniocalcin 2 gene MP:0000202 abnormal circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:18258678 733904 Stc2 stanniocalcin 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18258678 733904 Stc2 stanniocalcin 2 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:18258678 733904 Stc2 stanniocalcin 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18258678 733904 Stc2 stanniocalcin 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:21746875 733904 Stc2 stanniocalcin 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21746875 733904 Stc2 stanniocalcin 2 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:21746875 733904 Stc2 stanniocalcin 2 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:21746875 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:21584905 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0001123 dilated uterus IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16061471 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20210128 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20230601 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:14668204 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:14668204 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20210128 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:14668204 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16061471 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0002188 small heart IEA N RGD:5509061 20201022 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20141003 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210826 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:14668204 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20210128 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0003587 ureter obstruction IAGP N RGD:5509061 20141003 MGI PMID:16061471 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20141003 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0008289 abnormal adrenal medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0009082 uterus cyst IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14668204 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21584905 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14668204 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16061471 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011303 absent kidney papilla IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011305 dilated kidney calyx IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011305 dilated kidney calyx IAGP N RGD:5509061 20141003 MGI PMID:14668204 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011376 abnormal kidney corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011422 kidney medulla atrophy IAGP N RGD:5509061 20141003 MGI PMID:14668204 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011422 kidney medulla atrophy IAGP N RGD:5509061 20141003 MGI PMID:21584905 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20141003 MGI PMID:14668204 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011460 decreased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011487 abnormal ureteropelvic junction morphology IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011491 ureteropelvic junction obstruction IAGP N RGD:5509061 20141003 MGI PMID:10811842 733905 Adamts1 ADAM metallopeptidase with thrombospondin type 1 motif 1 gene MP:0011565 kidney papillary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10811842 733915 Krt19 keratin 19 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:16207837 733915 Krt19 keratin 19 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21502497 733915 Krt19 keratin 19 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20181129 MGI PMID:27032374 733915 Krt19 keratin 19 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20181129 MGI PMID:27032374 733915 Krt19 keratin 19 gene MP:0000652 enlarged sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:21502497 733915 Krt19 keratin 19 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18519586 733915 Krt19 keratin 19 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11013209 733915 Krt19 keratin 19 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 733915 Krt19 keratin 19 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 733915 Krt19 keratin 19 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 733915 Krt19 keratin 19 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20181129 MGI PMID:27032374 733915 Krt19 keratin 19 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20181129 MGI PMID:27032374 733915 Krt19 keratin 19 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21502497 733915 Krt19 keratin 19 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:21502497 733915 Krt19 keratin 19 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10545105 733915 Krt19 keratin 19 gene MP:0002083 premature death IAGP N RGD:5509061 20181129 MGI PMID:27032374 733915 Krt19 keratin 19 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11013209 733915 Krt19 keratin 19 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11062258 733915 Krt19 keratin 19 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18543299 733915 Krt19 keratin 19 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10545105 733915 Krt19 keratin 19 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16207837 733915 Krt19 keratin 19 gene MP:0002785 absent Leydig cells IAGP N RGD:5509061 20141003 MGI PMID:16207837 733915 Krt19 keratin 19 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:16207837 733915 Krt19 keratin 19 gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141204 MGI PMID:25105579 733915 Krt19 keratin 19 gene MP:0003780 increased lip tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21502497 733915 Krt19 keratin 19 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:16207837 733915 Krt19 keratin 19 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11062258 733915 Krt19 keratin 19 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:16015579 733915 Krt19 keratin 19 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 733915 Krt19 keratin 19 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:11013209 733915 Krt19 keratin 19 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:11062258 733915 Krt19 keratin 19 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 733915 Krt19 keratin 19 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11013209 733915 Krt19 keratin 19 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 733915 Krt19 keratin 19 gene MP:0005084 abnormal gallbladder morphology IAGP N RGD:5509061 20181129 MGI PMID:27032374 733915 Krt19 keratin 19 gene MP:0005488 bronchial epithelial hyperplasia IAGP N RGD:5509061 20181129 MGI PMID:27032374 733915 Krt19 keratin 19 gene MP:0006372 impaired placental function IAGP N RGD:5509061 20141003 MGI PMID:11062258 733915 Krt19 keratin 19 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:16015579 733915 Krt19 keratin 19 gene MP:0006424 absent testis cords IAGP N RGD:5509061 20141003 MGI PMID:16207837 733915 Krt19 keratin 19 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 733915 Krt19 keratin 19 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:16015579 733915 Krt19 keratin 19 gene MP:0008959 abnormal spongiotrophoblast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 733915 Krt19 keratin 19 gene MP:0009139 failure of Mullerian duct regression IAGP N RGD:5509061 20141003 MGI PMID:16207837 733915 Krt19 keratin 19 gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20181129 MGI PMID:27032374 733915 Krt19 keratin 19 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:16015579 733915 Krt19 keratin 19 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:16015579 733915 Krt19 keratin 19 gene MP:0009241 thick sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:16015579 733915 Krt19 keratin 19 gene MP:0009343 dilated gallbladder IAGP N RGD:5509061 20181129 MGI PMID:27032374 733915 Krt19 keratin 19 gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20141003 MGI PMID:16015579 733915 Krt19 keratin 19 gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:11062258 733915 Krt19 keratin 19 gene MP:0009493 abnormal cystic duct morphology IAGP N RGD:5509061 20181129 MGI PMID:27032374 733915 Krt19 keratin 19 gene MP:0009498 abnormal extrahepatic bile duct morphology IAGP N RGD:5509061 20181129 MGI PMID:27032374 733915 Krt19 keratin 19 gene MP:0009535 abnormal skin sebaceous gland morphology IAGP N RGD:5509061 20141003 MGI PMID:21502497 733915 Krt19 keratin 19 gene MP:0009794 sebaceous gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21502497 733915 Krt19 keratin 19 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20160512 MGI PMID:21502497 733915 Krt19 keratin 19 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21502497 733915 Krt19 keratin 19 gene MP:0010799 stomach mucosa hyperplasia IAGP N RGD:5509061 20181129 MGI PMID:27032374 733915 Krt19 keratin 19 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11013209 733915 Krt19 keratin 19 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11062258 733915 Krt19 keratin 19 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18519586 733915 Krt19 keratin 19 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16207837 733915 Krt19 keratin 19 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11062258 733915 Krt19 keratin 19 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21502497 733915 Krt19 keratin 19 gene MP:0012756 impaired cranial neural crest cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16207837 733915 Krt19 keratin 19 gene MP:0030574 increased hair follicle cell proliferation IAGP N RGD:5509061 20181129 MGI PMID:21502497 733915 Krt19 keratin 19 gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20191219 MGI PMID:11062258 733916 S100a8 S100 calcium binding protein A8 (calgranulin A) gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10438963 733916 S100a8 S100 calcium binding protein A8 (calgranulin A) gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10438963 733916 S100a8 S100 calcium binding protein A8 (calgranulin A) gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22016186 733916 S100a8 S100 calcium binding protein A8 (calgranulin A) gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10438963 733916 S100a8 S100 calcium binding protein A8 (calgranulin A) gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22016186 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:1237429 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:6708965 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000738 impaired muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:6708965 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000738 impaired muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:6708966 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:23187123 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:6692971 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:7286424 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:6692972 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0001575 cyanosis IEA N RGD:5509061 20210520 MGI 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:1663002 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:23187123 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20170223 MGI PMID:26965373 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:7286424 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:6692971 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:6692972 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:7286424 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:4738109 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:8143864 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:8462749 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20170223 MGI PMID:26965373 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20170223 MGI PMID:26965373 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:5041196 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:8143864 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:8462749 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0003201 extremity edema IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0003201 extremity edema IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20160811 MGI 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20160811 MGI 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:6692971 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:6692972 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004089 dilated sarcoplasmic reticulum IAGP N RGD:5509061 20141003 MGI PMID:23187123 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004089 dilated sarcoplasmic reticulum IAGP N RGD:5509061 20141003 MGI PMID:5041196 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:8143864 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:5041196 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:8143864 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20170223 MGI PMID:26965373 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004198 abnormal fetal size IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20170223 MGI PMID:26965373 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004338 small clavicle IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004343 small scapula IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004386 enlarged interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004623 thoracic vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004671 long ribs IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004674 thin ribs IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004733 abnormal thoracic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0004846 absent skeletal muscle IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:14300096 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0005388 respiratory system phenotype IEA N RGD:5509061 20160421 MGI 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210520 MGI 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:7286424 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:8666981 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20170223 MGI PMID:26965373 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:23187123 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20170223 MGI PMID:26965373 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0008150 decreased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:23187123 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20170223 MGI PMID:26965373 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23187123 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20170223 MGI PMID:26965373 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20170223 MGI PMID:26965373 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20170223 MGI PMID:26965373 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0011632 dilated mitochondrion IAGP N RGD:5509061 20170223 MGI PMID:26965373 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0014344 abnormal skeletal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:26965373 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0030258 small mandibular condyloid process IAGP N RGD:5509061 20171019 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0030283 small mandibular coronoid process IAGP N RGD:5509061 20171102 MGI PMID:14300095 733918 Cacna1s calcium channel, voltage-dependent, L type, alpha 1S subunit gene MP:0030287 enlarged occipital bone IAGP N RGD:5509061 20171102 MGI PMID:14300095 733919 Prdx5 peroxiredoxin 5 gene MP:0001260 increased body weight IAGP N RGD:5509061 20201015 MGI PMID:29777756 733919 Prdx5 peroxiredoxin 5 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20201015 MGI PMID:29777756 733919 Prdx5 peroxiredoxin 5 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20201015 MGI PMID:29777756 733919 Prdx5 peroxiredoxin 5 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20210722 MGI PMID:30044981 733919 Prdx5 peroxiredoxin 5 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20201015 MGI PMID:29777756 733919 Prdx5 peroxiredoxin 5 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20210722 MGI PMID:30044981 733919 Prdx5 peroxiredoxin 5 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20210722 MGI PMID:30044981 733919 Prdx5 peroxiredoxin 5 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20210722 MGI PMID:30044981 733919 Prdx5 peroxiredoxin 5 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20201015 MGI PMID:29777756 733919 Prdx5 peroxiredoxin 5 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20201015 MGI PMID:29777756 733919 Prdx5 peroxiredoxin 5 gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20201015 MGI PMID:29777756 733919 Prdx5 peroxiredoxin 5 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20201015 MGI PMID:29777756 733919 Prdx5 peroxiredoxin 5 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20201015 MGI PMID:29777756 733919 Prdx5 peroxiredoxin 5 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20201015 MGI PMID:29777756 733919 Prdx5 peroxiredoxin 5 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20210722 MGI PMID:30044981 733919 Prdx5 peroxiredoxin 5 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20210722 MGI PMID:30044981 733919 Prdx5 peroxiredoxin 5 gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20210722 MGI PMID:30044981 733919 Prdx5 peroxiredoxin 5 gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20210722 MGI PMID:30044981 733919 Prdx5 peroxiredoxin 5 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20210722 MGI PMID:30044981 733919 Prdx5 peroxiredoxin 5 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20201015 MGI PMID:29777756 733919 Prdx5 peroxiredoxin 5 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20210722 MGI PMID:30044981 733919 Prdx5 peroxiredoxin 5 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20210722 MGI PMID:30044981 733919 Prdx5 peroxiredoxin 5 gene MP:0031269 increased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210722 MGI PMID:29777756 733922 Hbp1 high mobility group box transcription factor 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20191017 MGI PMID:26041766 733922 Hbp1 high mobility group box transcription factor 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20191017 MGI PMID:26041766 733922 Hbp1 high mobility group box transcription factor 1 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20191017 MGI PMID:26041766 733922 Hbp1 high mobility group box transcription factor 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20191017 MGI PMID:26041766 733922 Hbp1 high mobility group box transcription factor 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20191017 MGI PMID:26041766 733922 Hbp1 high mobility group box transcription factor 1 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20191017 MGI PMID:26041766 733922 Hbp1 high mobility group box transcription factor 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20191017 MGI PMID:26041766 733922 Hbp1 high mobility group box transcription factor 1 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20191017 MGI PMID:26041766 733922 Hbp1 high mobility group box transcription factor 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20191017 MGI PMID:26041766 733922 Hbp1 high mobility group box transcription factor 1 gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20191017 MGI PMID:26041766 733922 Hbp1 high mobility group box transcription factor 1 gene MP:0012206 increased neuronal stem cell self-renewal IAGP N RGD:5509061 20191017 MGI PMID:26041766 733922 Hbp1 high mobility group box transcription factor 1 gene MP:0014558 decreased cortical ventricular zone thickness IAGP N RGD:5509061 20241031 MGI PMID:26041766 733922 Hbp1 high mobility group box transcription factor 1 gene MP:0030004 hippocampus hypoplasia IAGP N RGD:5509061 20191017 MGI PMID:26041766 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:11425898 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17426285 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:18579678 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:15496443 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10205173 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10804175 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:18579678 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0002653 abnormal ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0002659 pituitary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17426285 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10205173 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:15496443 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0003647 absent oligodendrocytes IAGP N RGD:5509061 20141003 MGI PMID:15496443 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141003 MGI PMID:17426285 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0003817 abnormal pituitary diverticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:17426285 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0004164 abnormal neurohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:17426285 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18579678 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15496443 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0004327 increased vestibular hair cell number IAGP N RGD:5509061 20141003 MGI PMID:11425898 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:11425898 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:11425898 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10821751 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0005603 neuron hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:10205173 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:11425898 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11425898 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0006292 abnormal nasal placode morphology IAGP N RGD:5509061 20141003 MGI PMID:10804175 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0006294 absent optic vesicle IAGP N RGD:5509061 20141003 MGI PMID:15496443 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0008328 increased somatotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:17426285 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0008367 absent pituitary intermediate lobe IAGP N RGD:5509061 20141003 MGI PMID:17426285 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0008934 absent choroid plexus IAGP N RGD:5509061 20141003 MGI PMID:18579678 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0008949 increased Cajal-Retzius cell number IAGP N RGD:5509061 20141003 MGI PMID:18579678 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0009463 abnormal pituitary infundibular stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:17426285 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18579678 733924 Hes5 hes family bHLH transcription factor 5 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15496443 733927 Vldlr very low density lipoprotein receptor gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220811 MGI 733927 Vldlr very low density lipoprotein receptor gene MP:0000274 enlarged heart IEA N RGD:5509061 20220811 MGI 733927 Vldlr very low density lipoprotein receptor gene MP:0000414 alopecia IEA N RGD:5509061 20190523 MGI 733927 Vldlr very low density lipoprotein receptor gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 733927 Vldlr very low density lipoprotein receptor gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10380922 733927 Vldlr very low density lipoprotein receptor gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16481437 733927 Vldlr very low density lipoprotein receptor gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:10380922 733927 Vldlr very low density lipoprotein receptor gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:10380922 733927 Vldlr very low density lipoprotein receptor gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17330141 733927 Vldlr very low density lipoprotein receptor gene MP:0000791 delaminated cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16481437 733927 Vldlr very low density lipoprotein receptor gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16481437 733927 Vldlr very low density lipoprotein receptor gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:16481437 733927 Vldlr very low density lipoprotein receptor gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:10380922 733927 Vldlr very low density lipoprotein receptor gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:16481437 733927 Vldlr very low density lipoprotein receptor gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 733927 Vldlr very low density lipoprotein receptor gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 733927 Vldlr very low density lipoprotein receptor gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10380922 733927 Vldlr very low density lipoprotein receptor gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:10380922 733927 Vldlr very low density lipoprotein receptor gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:16481437 733927 Vldlr very low density lipoprotein receptor gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:10380922 733927 Vldlr very low density lipoprotein receptor gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 733927 Vldlr very low density lipoprotein receptor gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:16481437 733927 Vldlr very low density lipoprotein receptor gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:10380922 733927 Vldlr very low density lipoprotein receptor gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:21757581 733927 Vldlr very low density lipoprotein receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7667310 733927 Vldlr very low density lipoprotein receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10380922 733927 Vldlr very low density lipoprotein receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16481437 733927 Vldlr very low density lipoprotein receptor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7667310 733927 Vldlr very low density lipoprotein receptor gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:17562991 733927 Vldlr very low density lipoprotein receptor gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:18172119 733927 Vldlr very low density lipoprotein receptor gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:21757581 733927 Vldlr very low density lipoprotein receptor gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:17562991 733927 Vldlr very low density lipoprotein receptor gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:18172119 733927 Vldlr very low density lipoprotein receptor gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 733927 Vldlr very low density lipoprotein receptor gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10380922 733927 Vldlr very low density lipoprotein receptor gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16481437 733927 Vldlr very low density lipoprotein receptor gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12167620 733927 Vldlr very low density lipoprotein receptor gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10380922 733927 Vldlr very low density lipoprotein receptor gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16481437 733927 Vldlr very low density lipoprotein receptor gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20231207 MGI 733927 Vldlr very low density lipoprotein receptor gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12167620 733927 Vldlr very low density lipoprotein receptor gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12167620 733927 Vldlr very low density lipoprotein receptor gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12167620 733927 Vldlr very low density lipoprotein receptor gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:16481437 733927 Vldlr very low density lipoprotein receptor gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15840700 733927 Vldlr very low density lipoprotein receptor gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:12167620 733927 Vldlr very low density lipoprotein receptor gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10380922 733927 Vldlr very low density lipoprotein receptor gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12167620 733927 Vldlr very low density lipoprotein receptor gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21757581 733927 Vldlr very low density lipoprotein receptor gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:12972764 733927 Vldlr very low density lipoprotein receptor gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:21743011 733927 Vldlr very low density lipoprotein receptor gene MP:0003711 pathological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:12972764 733927 Vldlr very low density lipoprotein receptor gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21757581 733927 Vldlr very low density lipoprotein receptor gene MP:0004021 abnormal rod electrophysiology IEA N RGD:5509061 20190523 MGI 733927 Vldlr very low density lipoprotein receptor gene MP:0004022 abnormal cone electrophysiology IEA N RGD:5509061 20190523 MGI 733927 Vldlr very low density lipoprotein receptor gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 733927 Vldlr very low density lipoprotein receptor gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 733927 Vldlr very low density lipoprotein receptor gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 733927 Vldlr very low density lipoprotein receptor gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21757581 733927 Vldlr very low density lipoprotein receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15840700 733927 Vldlr very low density lipoprotein receptor gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17562991 733927 Vldlr very low density lipoprotein receptor gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18172119 733927 Vldlr very low density lipoprotein receptor gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21757581 733927 Vldlr very low density lipoprotein receptor gene MP:0005546 choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:12972764 733927 Vldlr very low density lipoprotein receptor gene MP:0005546 choroidal neovascularization IAGP N RGD:5509061 20141003 MGI PMID:18172119 733927 Vldlr very low density lipoprotein receptor gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17562991 733927 Vldlr very low density lipoprotein receptor gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:18172119 733927 Vldlr very low density lipoprotein receptor gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:21757581 733927 Vldlr very low density lipoprotein receptor gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:17562991 733927 Vldlr very low density lipoprotein receptor gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:17562991 733927 Vldlr very low density lipoprotein receptor gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:18172119 733927 Vldlr very low density lipoprotein receptor gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:18172119 733927 Vldlr very low density lipoprotein receptor gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:17562991 733927 Vldlr very low density lipoprotein receptor gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:18172119 733927 Vldlr very low density lipoprotein receptor gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:21743011 733927 Vldlr very low density lipoprotein receptor gene MP:0009084 blind uterus IEA N RGD:5509061 20201022 MGI 733927 Vldlr very low density lipoprotein receptor gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:7667310 733927 Vldlr very low density lipoprotein receptor gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20180301 MGI PMID:10380922 733927 Vldlr very low density lipoprotein receptor gene MP:0010098 abnormal retina blood vessel pattern IEA N RGD:5509061 20190523 MGI 733927 Vldlr very low density lipoprotein receptor gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10380922 733927 Vldlr very low density lipoprotein receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16481437 733927 Vldlr very low density lipoprotein receptor gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20180927 MGI 733927 Vldlr very low density lipoprotein receptor gene MP:0012329 increased circulating factor VIII level IAGP N RGD:5509061 20201002 MGI PMID:15840700 733927 Vldlr very low density lipoprotein receptor gene MP:0013146 eye lesions IEA N RGD:5509061 20180927 MGI 733927 Vldlr very low density lipoprotein receptor gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 733927 Vldlr very low density lipoprotein receptor gene MP:0030956 abnormal neuronal precursor cell migration IAGP N RGD:5509061 20190725 MGI PMID:17494763 733929 Tle3 transducin-like enhancer of split 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220519 MGI 733929 Tle3 transducin-like enhancer of split 3 gene MP:0000692 small spleen IEA N RGD:5509061 20220519 MGI 733929 Tle3 transducin-like enhancer of split 3 gene MP:0000774 decreased brain size IEA N RGD:5509061 20220519 MGI 733929 Tle3 transducin-like enhancer of split 3 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20220811 MGI 733929 Tle3 transducin-like enhancer of split 3 gene MP:0001147 small testis IEA N RGD:5509061 20220811 MGI 733929 Tle3 transducin-like enhancer of split 3 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220519 MGI 733929 Tle3 transducin-like enhancer of split 3 gene MP:0001304 cataract IEA N RGD:5509061 20220519 MGI 733929 Tle3 transducin-like enhancer of split 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22434868 733929 Tle3 transducin-like enhancer of split 3 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:22434868 733929 Tle3 transducin-like enhancer of split 3 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20220519 MGI 733929 Tle3 transducin-like enhancer of split 3 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 733929 Tle3 transducin-like enhancer of split 3 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:23473036 733929 Tle3 transducin-like enhancer of split 3 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:22434868 733929 Tle3 transducin-like enhancer of split 3 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:22434868 733929 Tle3 transducin-like enhancer of split 3 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:23473036 733929 Tle3 transducin-like enhancer of split 3 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21459326 733929 Tle3 transducin-like enhancer of split 3 gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22434868 733929 Tle3 transducin-like enhancer of split 3 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22434868 733929 Tle3 transducin-like enhancer of split 3 gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:23473036 733929 Tle3 transducin-like enhancer of split 3 gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23473036 733929 Tle3 transducin-like enhancer of split 3 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22434868 733929 Tle3 transducin-like enhancer of split 3 gene MP:0009179 abnormal pancreatic alpha cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22434868 733929 Tle3 transducin-like enhancer of split 3 gene MP:0009183 abnormal pancreatic delta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22434868 733929 Tle3 transducin-like enhancer of split 3 gene MP:0009188 abnormal PP cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22434868 733929 Tle3 transducin-like enhancer of split 3 gene MP:0009189 abnormal pancreatic epsilon cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22434868 733929 Tle3 transducin-like enhancer of split 3 gene MP:0009193 abnormal pancreatic epsilon cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22434868 733929 Tle3 transducin-like enhancer of split 3 gene MP:0011016 increased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:23473036 733929 Tle3 transducin-like enhancer of split 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21459326 733929 Tle3 transducin-like enhancer of split 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22434868 733929 Tle3 transducin-like enhancer of split 3 gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20141003 MGI PMID:21459326 733929 Tle3 transducin-like enhancer of split 3 gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20180125 MGI PMID:23473036 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0000745 tremors IEA N RGD:5509061 20201231 MGI 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:21147989 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20200402 MGI 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20200402 MGI 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:14651847 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:18936078 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:14651847 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14651847 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18936078 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:21147989 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:14651847 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:14651847 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0002807 abnormal eye blink conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:14651847 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20190502 MGI 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:21593326 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20151008 MGI PMID:24218458 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0003928 increased heart rate variability IAGP N RGD:5509061 20151008 MGI PMID:24218458 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0004085 abnormal heartbeat IAGP N RGD:5509061 20151008 MGI PMID:24218458 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:21903939 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20190103 MGI 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:21903939 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21147989 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20151008 MGI PMID:24218458 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0009946 abnormal olfactory bulb layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21147989 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21147989 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0010057 abnormal olfactory bulb outer nerve layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21147989 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0010504 abnormal RR interval IAGP N RGD:5509061 20151008 MGI PMID:24218458 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210128 MGI 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0010520 sinoatrial block IAGP N RGD:5509061 20151008 MGI PMID:24218458 733931 Hcn1 hyperpolarization activated cyclic nucleotide gated potassium channel 1 gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20151008 MGI PMID:24218458 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19270340 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:19270340 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19270340 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:19270340 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20200528 MGI PMID:31412538 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20200528 MGI PMID:31412538 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20200528 MGI PMID:31412538 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:19270340 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0002794 lenticonus IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0003063 increased coping response IAGP N RGD:5509061 20200528 MGI PMID:31412538 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0003908 decreased stereotypic behavior IAGP N RGD:5509061 20200528 MGI PMID:31412538 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12874108 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:19270340 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:19270340 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20210819 MGI PMID:31412538 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20210819 MGI PMID:31412538 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20141003 MGI PMID:19270340 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0010734 abnormal paranode morphology IAGP N RGD:5509061 20141003 MGI PMID:19270340 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0010735 abnormal paranodal axoglial junction morphology IAGP N RGD:5509061 20141003 MGI PMID:19270340 733937 Gnpat glyceronephosphate O-acyltransferase gene MP:0020422 decreased freezing behavior IAGP N RGD:5509061 20200528 MGI PMID:31412538 733940 Cuzd1 CUB and zona pellucida-like domains 1 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20170817 MGI PMID:28278176 733940 Cuzd1 CUB and zona pellucida-like domains 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20170817 MGI PMID:28278176 733940 Cuzd1 CUB and zona pellucida-like domains 1 gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20141003 MGI PMID:12401800 733940 Cuzd1 CUB and zona pellucida-like domains 1 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20170817 MGI PMID:28278176 733940 Cuzd1 CUB and zona pellucida-like domains 1 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20170817 MGI PMID:28278176 733940 Cuzd1 CUB and zona pellucida-like domains 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12401800 733940 Cuzd1 CUB and zona pellucida-like domains 1 gene MP:0010174 decreased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20170817 MGI PMID:28278176 733940 Cuzd1 CUB and zona pellucida-like domains 1 gene MP:0012075 impaired mammary gland growth during pregnancy IAGP N RGD:5509061 20170817 MGI PMID:28278176 733942 Dctn4 dynactin 4 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20211021 MGI 733942 Dctn4 dynactin 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733944 Herpud1 homocysteine-inducible, endoplasmic reticulum stress-inducible, ubiquitin-like domain member 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22479592 733944 Herpud1 homocysteine-inducible, endoplasmic reticulum stress-inducible, ubiquitin-like domain member 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22479592 733944 Herpud1 homocysteine-inducible, endoplasmic reticulum stress-inducible, ubiquitin-like domain member 1 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:22479592 733948 Cul5 cullin 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 733948 Cul5 cullin 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 733948 Cul5 cullin 5 gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20181227 MGI 733948 Cul5 cullin 5 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 733948 Cul5 cullin 5 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20181227 MGI 733948 Cul5 cullin 5 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 733948 Cul5 cullin 5 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20220811 MGI 733948 Cul5 cullin 5 gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 733948 Cul5 cullin 5 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 733948 Cul5 cullin 5 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 733948 Cul5 cullin 5 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180315 MGI PMID:28522566 733948 Cul5 cullin 5 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20180315 MGI PMID:28522566 733948 Cul5 cullin 5 gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20180315 MGI PMID:28522566 733948 Cul5 cullin 5 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20180315 MGI PMID:28522566 733948 Cul5 cullin 5 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180315 MGI PMID:28522566 733948 Cul5 cullin 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733948 Cul5 cullin 5 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220519 MGI 733950 Angptl2 angiopoietin-like 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19723494 733950 Angptl2 angiopoietin-like 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19723494 733950 Angptl2 angiopoietin-like 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:19723494 733950 Angptl2 angiopoietin-like 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19723494 733950 Angptl2 angiopoietin-like 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19723494 733950 Angptl2 angiopoietin-like 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19723494 733950 Angptl2 angiopoietin-like 2 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:19723494 733953 Btg3 BTG anti-proliferation factor 3 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19068083 733953 Btg3 BTG anti-proliferation factor 3 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19068083 733953 Btg3 BTG anti-proliferation factor 3 gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19068083 733953 Btg3 BTG anti-proliferation factor 3 gene MP:0014167 ectopic bone IAGP N RGD:5509061 20160407 MGI PMID:19234306 733954 Cxcr1 C-X-C motif chemokine receptor 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 733954 Cxcr1 C-X-C motif chemokine receptor 1 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 733954 Cxcr1 C-X-C motif chemokine receptor 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 733954 Cxcr1 C-X-C motif chemokine receptor 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210128 MGI 733954 Cxcr1 C-X-C motif chemokine receptor 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 733954 Cxcr1 C-X-C motif chemokine receptor 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20200402 MGI 733955 Slc26a1 solute carrier family 26 (sulfate transporter), member 1 gene MP:0000192 abnormal mineral level IAGP N RGD:5509061 20141003 MGI PMID:20160351 733955 Slc26a1 solute carrier family 26 (sulfate transporter), member 1 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:20160351 733955 Slc26a1 solute carrier family 26 (sulfate transporter), member 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:20160351 733955 Slc26a1 solute carrier family 26 (sulfate transporter), member 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:20160351 733955 Slc26a1 solute carrier family 26 (sulfate transporter), member 1 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:20160351 733955 Slc26a1 solute carrier family 26 (sulfate transporter), member 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:20160351 733955 Slc26a1 solute carrier family 26 (sulfate transporter), member 1 gene MP:0002708 nephrolithiasis IAGP N RGD:5509061 20141003 MGI PMID:20160351 733955 Slc26a1 solute carrier family 26 (sulfate transporter), member 1 gene MP:0002853 hyposulfatemia IAGP N RGD:5509061 20141003 MGI PMID:20160351 733955 Slc26a1 solute carrier family 26 (sulfate transporter), member 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20160351 733955 Slc26a1 solute carrier family 26 (sulfate transporter), member 1 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:20160351 733955 Slc26a1 solute carrier family 26 (sulfate transporter), member 1 gene MP:0008546 abnormal vesicle-mediated transport IAGP N RGD:5509061 20141003 MGI PMID:20160351 733955 Slc26a1 solute carrier family 26 (sulfate transporter), member 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20160351 733955 Slc26a1 solute carrier family 26 (sulfate transporter), member 1 gene MP:0009472 increased urine sulfate level IAGP N RGD:5509061 20141003 MGI PMID:20160351 733960 Nme7 NME/NM23 family member 7 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:20080492 733960 Nme7 NME/NM23 family member 7 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:21746835 733960 Nme7 NME/NM23 family member 7 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:20080492 733960 Nme7 NME/NM23 family member 7 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:20080492 733960 Nme7 NME/NM23 family member 7 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:20080492 733960 Nme7 NME/NM23 family member 7 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:21746835 733960 Nme7 NME/NM23 family member 7 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:20080492 733960 Nme7 NME/NM23 family member 7 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:21746835 733960 Nme7 NME/NM23 family member 7 gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:20080492 733960 Nme7 NME/NM23 family member 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 733964 Ceacam9 CEA cell adhesion molecule 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10982830 733964 Ceacam9 CEA cell adhesion molecule 9 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12482980 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17060636 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20230119 MGI 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:11830666 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20230119 MGI 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:17060636 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0002334 abnormal airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:11877470 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11830666 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20141003 MGI PMID:11830666 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20141003 MGI PMID:11877470 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0002602 abnormal eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11830666 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11830666 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11830666 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11877470 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17060636 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0008603 decreased circulating interleukin-4 level IAGP N RGD:5509061 20141003 MGI PMID:17060636 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:11830666 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:11877470 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0008724 impaired eosinophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:11830666 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:11830666 733966 Ccr3 C-C motif chemokine receptor 3 gene MP:0009676 abnormal hemostasis IAGP N RGD:5509061 20141003 MGI PMID:17060636 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:12692538 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:10195897 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10229185 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10359587 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0000608 dissociated hepatocytes IAGP N RGD:5509061 20141003 MGI PMID:10195897 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:18606991 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:10898787 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10898787 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:10898787 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:10898787 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:24211183 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:24211183 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:24211183 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18606991 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:14499113 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:12707341 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12707341 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20200806 MGI PMID:30337470 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:14983030 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10195897 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18606991 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24211183 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14499113 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0002418 increased susceptibility to viral infection IEA N RGD:5509061 20151112 MGI 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0002459 abnormal B cell physiology IEA N RGD:5509061 20151112 MGI 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:14499113 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18606991 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18606991 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:10898787 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:10195897 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:10229185 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:10359587 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:10898787 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:12692538 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20231695 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10195897 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10229185 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10898787 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10195897 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0004574 broad limb buds IAGP N RGD:5509061 20141003 MGI PMID:10898787 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0004838 abnormal neural fold elevation formation IAGP N RGD:5509061 20141003 MGI PMID:10898787 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:24211183 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20200806 MGI PMID:30337470 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:14499113 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235208 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12707341 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12707341 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20200806 MGI PMID:30337470 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:14499113 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20200806 MGI PMID:30337470 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005025 abnormal response to infection IEA N RGD:5509061 20151112 MGI 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:12692538 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12707341 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:18606991 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12235208 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:12692538 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:18606991 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005415 intrahepatic cholestasis IAGP N RGD:5509061 20141003 MGI PMID:18606991 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17292824 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10195897 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10229185 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10898787 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:14499113 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14499113 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20200806 MGI PMID:30337470 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14499113 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200806 MGI PMID:30337470 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20151112 MGI 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14499113 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235208 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235208 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12707341 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235208 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:12235208 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:12707341 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:12692538 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:12235208 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:14499113 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:12692538 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:20231695 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20231695 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008729 decreased memory B cell number IAGP N RGD:5509061 20200806 MGI PMID:30337470 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:18606991 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18606991 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12707341 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008885 increased enterocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14983030 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0008991 abnormal bile canaliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:18606991 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0009405 increased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:18299349 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IAGP N RGD:5509061 20210923 MGI PMID:33658989 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0010842 decreased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190606 MGI 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12202685 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24211183 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14499113 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10195897 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10359587 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10898787 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10229185 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10898787 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0011706 abnormal fibroblast migration IAGP N RGD:5509061 20141003 MGI PMID:20231695 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20170223 MGI PMID:20231695 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10898787 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10898787 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0013182 increased spinal cord apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10898787 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:10195897 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:10229185 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:14499113 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0013762 abnormal effector T cell number IAGP N RGD:5509061 20200806 MGI PMID:30337470 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0020002 increased response to antigen IEA N RGD:5509061 20151112 MGI 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0020416 decreased fibroblast chemotaxis IAGP N RGD:5509061 20170223 MGI PMID:20231695 733969 Ikbkb inhibitor of kappaB kinase beta gene MP:0030957 abnormal myotube morphology IAGP N RGD:5509061 20190725 MGI PMID:18299349 733975 Phf5a PHD finger protein 5A gene MP:0000692 small spleen IAGP N RGD:5509061 20240328 MGI PMID:38095286 733975 Phf5a PHD finger protein 5A gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20240328 MGI PMID:38095286 733975 Phf5a PHD finger protein 5A gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20240328 MGI PMID:38095286 733975 Phf5a PHD finger protein 5A gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20240328 MGI PMID:38095286 733975 Phf5a PHD finger protein 5A gene MP:0006205 embryonic lethality between implantation and somite formation IEA N RGD:5509061 20141003 MGI 733975 Phf5a PHD finger protein 5A gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20240328 MGI PMID:38095286 733975 Phf5a PHD finger protein 5A gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20240328 MGI PMID:38095286 733975 Phf5a PHD finger protein 5A gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20240328 MGI PMID:38095286 733975 Phf5a PHD finger protein 5A gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20240328 MGI PMID:38095286 733975 Phf5a PHD finger protein 5A gene MP:0008766 abnormal B cell receptor editing IAGP N RGD:5509061 20240328 MGI PMID:38095286 733975 Phf5a PHD finger protein 5A gene MP:0011815 increased pre-pro B cell number IAGP N RGD:5509061 20240328 MGI PMID:38095286 733975 Phf5a PHD finger protein 5A gene MP:0014403 decreased early pro-B cell number IAGP N RGD:5509061 20240405 MGI PMID:38095286 733975 Phf5a PHD finger protein 5A gene MP:0014404 decreased late pro-B cell number IAGP N RGD:5509061 20240405 MGI PMID:38095286 733978 Dpep1 dipeptidase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9560193 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20220317 MGI PMID:33791800 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:14672995 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0003438 abnormal carotid body physiology IAGP N RGD:5509061 20141003 MGI PMID:14672995 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20220317 MGI PMID:33791800 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20220317 MGI PMID:33791800 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20220317 MGI PMID:33791800 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0004562 abnormal inner hair cell synaptic ribbon morphology IAGP N RGD:5509061 20220317 MGI PMID:33791800 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0005576 decreased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:14672995 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:14672995 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14672995 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0011806 decreased dermal fibroblast proliferation IAGP N RGD:5509061 20220317 MGI PMID:33791800 733980 P2rx2 purinergic receptor P2X, ligand-gated ion channel, 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20220317 MGI PMID:33791800 733982 Faf1 Fas-associated factor 1 gene MP:0000745 tremors IEA N RGD:5509061 20240523 MGI 733982 Faf1 Fas-associated factor 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23307929 733982 Faf1 Fas-associated factor 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20200514 MGI 733982 Faf1 Fas-associated factor 1 gene MP:0001925 male infertility IEA N RGD:5509061 20230601 MGI 733982 Faf1 Fas-associated factor 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20200514 MGI 733982 Faf1 Fas-associated factor 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230601 MGI 733982 Faf1 Fas-associated factor 1 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20240523 MGI 733982 Faf1 Fas-associated factor 1 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:23307929 733982 Faf1 Fas-associated factor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23307929 733982 Faf1 Fas-associated factor 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18303090 733982 Faf1 Fas-associated factor 1 gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:23307929 733982 Faf1 Fas-associated factor 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20240523 MGI 733983 Mprip myosin phosphatase Rho interacting protein gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201022 MGI 733983 Mprip myosin phosphatase Rho interacting protein gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 733983 Mprip myosin phosphatase Rho interacting protein gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20201022 MGI 733983 Mprip myosin phosphatase Rho interacting protein gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 733983 Mprip myosin phosphatase Rho interacting protein gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 733983 Mprip myosin phosphatase Rho interacting protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 733986 Bcl2a1a B cell leukemia/lymphoma 2 related protein A1a gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:9841913 733986 Bcl2a1a B cell leukemia/lymphoma 2 related protein A1a gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11823517 733986 Bcl2a1a B cell leukemia/lymphoma 2 related protein A1a gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20190117 MGI PMID:28085150 733986 Bcl2a1a B cell leukemia/lymphoma 2 related protein A1a gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:11823517 733986 Bcl2a1a B cell leukemia/lymphoma 2 related protein A1a gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:9841913 733986 Bcl2a1a B cell leukemia/lymphoma 2 related protein A1a gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 733986 Bcl2a1a B cell leukemia/lymphoma 2 related protein A1a gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:11823517 733986 Bcl2a1a B cell leukemia/lymphoma 2 related protein A1a gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 733986 Bcl2a1a B cell leukemia/lymphoma 2 related protein A1a gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 733986 Bcl2a1a B cell leukemia/lymphoma 2 related protein A1a gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11823517 733986 Bcl2a1a B cell leukemia/lymphoma 2 related protein A1a gene MP:0010836 decreased CD4-positive, alpha-beta memory T cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 733986 Bcl2a1a B cell leukemia/lymphoma 2 related protein A1a gene MP:0010842 decreased central memory CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 733986 Bcl2a1a B cell leukemia/lymphoma 2 related protein A1a gene MP:0010845 decreased effector memory CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190117 MGI PMID:28085150 733992 Gys2 glycogen synthase 2 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20178984 733992 Gys2 glycogen synthase 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20160804 MGI 733992 Gys2 glycogen synthase 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 733992 Gys2 glycogen synthase 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20178984 733992 Gys2 glycogen synthase 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23990365 733992 Gys2 glycogen synthase 2 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20160804 MGI 733992 Gys2 glycogen synthase 2 gene MP:0002715 decreased glycogen catabolism rate IAGP N RGD:5509061 20141003 MGI PMID:20178984 733992 Gys2 glycogen synthase 2 gene MP:0002715 decreased glycogen catabolism rate IAGP N RGD:5509061 20141003 MGI PMID:23990365 733992 Gys2 glycogen synthase 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20178984 733992 Gys2 glycogen synthase 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23990365 733992 Gys2 glycogen synthase 2 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:20178984 733992 Gys2 glycogen synthase 2 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20160804 MGI 733992 Gys2 glycogen synthase 2 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:20178984 733992 Gys2 glycogen synthase 2 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:23990365 733992 Gys2 glycogen synthase 2 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20178984 733992 Gys2 glycogen synthase 2 gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20160804 MGI 733992 Gys2 glycogen synthase 2 gene MP:0003457 abnormal circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:20178984 733992 Gys2 glycogen synthase 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20178984 733992 Gys2 glycogen synthase 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23990365 733992 Gys2 glycogen synthase 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23990365 733992 Gys2 glycogen synthase 2 gene MP:0005439 decreased glycogen level IAGP N RGD:5509061 20141003 MGI PMID:20178984 733992 Gys2 glycogen synthase 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20178984 733992 Gys2 glycogen synthase 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23990365 733992 Gys2 glycogen synthase 2 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20160804 MGI 733992 Gys2 glycogen synthase 2 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20160804 MGI 733992 Gys2 glycogen synthase 2 gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20178984 733992 Gys2 glycogen synthase 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20178984 733992 Gys2 glycogen synthase 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23990365 733992 Gys2 glycogen synthase 2 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23990365 733992 Gys2 glycogen synthase 2 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:23990365 733992 Gys2 glycogen synthase 2 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:20178984 733992 Gys2 glycogen synthase 2 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20181011 MGI 733992 Gys2 glycogen synthase 2 gene MP:0030020 decreased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:20178984 733993 Xcl1 chemokine (C motif) ligand 1 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:21300913 733993 Xcl1 chemokine (C motif) ligand 1 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:21300913 733993 Xcl1 chemokine (C motif) ligand 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:21300913 733993 Xcl1 chemokine (C motif) ligand 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:21300913 733993 Xcl1 chemokine (C motif) ligand 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:21300913 733993 Xcl1 chemokine (C motif) ligand 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:21300913 733993 Xcl1 chemokine (C motif) ligand 1 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:21300913 733993 Xcl1 chemokine (C motif) ligand 1 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19913446 733993 Xcl1 chemokine (C motif) ligand 1 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21300913 733993 Xcl1 chemokine (C motif) ligand 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19913446 733993 Xcl1 chemokine (C motif) ligand 1 gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:19913446 733993 Xcl1 chemokine (C motif) ligand 1 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:21300913 733993 Xcl1 chemokine (C motif) ligand 1 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:21300913 733993 Xcl1 chemokine (C motif) ligand 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19913446 733993 Xcl1 chemokine (C motif) ligand 1 gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:21300913 733994 Tsc1 TSC complex subunit 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20220609 MGI PMID:28523278 733994 Tsc1 TSC complex subunit 1 gene MP:0000134 abnormal compact bone thickness IAGP N RGD:5509061 20220609 MGI PMID:28523278 733994 Tsc1 TSC complex subunit 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20220609 MGI PMID:28523278 733994 Tsc1 TSC complex subunit 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20220609 MGI PMID:28523278 733994 Tsc1 TSC complex subunit 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11875047 733994 Tsc1 TSC complex subunit 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15601645 733994 Tsc1 TSC complex subunit 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:21179166 733994 Tsc1 TSC complex subunit 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:21479224 733994 Tsc1 TSC complex subunit 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11875047 733994 Tsc1 TSC complex subunit 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21179166 733994 Tsc1 TSC complex subunit 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21479224 733994 Tsc1 TSC complex subunit 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:21179166 733994 Tsc1 TSC complex subunit 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18495876 733994 Tsc1 TSC complex subunit 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20151224 MGI PMID:23696872 733994 Tsc1 TSC complex subunit 1 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20150702 MGI PMID:22763451 733994 Tsc1 TSC complex subunit 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20150702 MGI PMID:22763451 733994 Tsc1 TSC complex subunit 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20150702 MGI PMID:22763451 733994 Tsc1 TSC complex subunit 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15888477 733994 Tsc1 TSC complex subunit 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:18495876 733994 Tsc1 TSC complex subunit 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19843540 733994 Tsc1 TSC complex subunit 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 733994 Tsc1 TSC complex subunit 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:22791749 733994 Tsc1 TSC complex subunit 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22791749 733994 Tsc1 TSC complex subunit 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20220609 MGI PMID:28523278 733994 Tsc1 TSC complex subunit 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220609 MGI PMID:28523278 733994 Tsc1 TSC complex subunit 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23666760 733994 Tsc1 TSC complex subunit 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20170202 MGI PMID:26777415 733994 Tsc1 TSC complex subunit 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20190516 MGI PMID:28250050 733994 Tsc1 TSC complex subunit 1 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20190516 MGI PMID:28250050 733994 Tsc1 TSC complex subunit 1 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20190516 MGI PMID:28250050 733994 Tsc1 TSC complex subunit 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20170202 MGI PMID:26777415 733994 Tsc1 TSC complex subunit 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20150702 MGI PMID:22763451 733994 Tsc1 TSC complex subunit 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20150702 MGI PMID:23250422 733994 Tsc1 TSC complex subunit 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20150702 MGI PMID:23250422 733994 Tsc1 TSC complex subunit 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20150702 MGI PMID:22763451 733994 Tsc1 TSC complex subunit 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18568033 733994 Tsc1 TSC complex subunit 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21179166 733994 Tsc1 TSC complex subunit 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17714952 733994 Tsc1 TSC complex subunit 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150702 MGI PMID:22763451 733994 Tsc1 TSC complex subunit 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20150702 MGI PMID:22763451 733994 Tsc1 TSC complex subunit 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20150702 MGI PMID:22763451 733994 Tsc1 TSC complex subunit 1 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17714952 733994 Tsc1 TSC complex subunit 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17714952 733994 Tsc1 TSC complex subunit 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:17714952 733994 Tsc1 TSC complex subunit 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17714952 733994 Tsc1 TSC complex subunit 1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20151224 MGI PMID:23696872 733994 Tsc1 TSC complex subunit 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:18568033 733994 Tsc1 TSC complex subunit 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:17714952 733994 Tsc1 TSC complex subunit 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15888477 733994 Tsc1 TSC complex subunit 1 gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:19843540 733994 Tsc1 TSC complex subunit 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:19843540 733994 Tsc1 TSC complex subunit 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21479224 733994 Tsc1 TSC complex subunit 1 gene MP:0001785 edema IAGP N RGD:5509061 20170202 MGI PMID:26777415 733994 Tsc1 TSC complex subunit 1 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:15601645 733994 Tsc1 TSC complex subunit 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20151224 MGI PMID:23696872 733994 Tsc1 TSC complex subunit 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:19843540 733994 Tsc1 TSC complex subunit 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0002045 increased renal cystadenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0002045 increased renal cystadenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11875047 733994 Tsc1 TSC complex subunit 1 gene MP:0002045 increased renal cystadenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15888477 733994 Tsc1 TSC complex subunit 1 gene MP:0002047 increased hepatic hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0002047 increased hepatic hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:11875047 733994 Tsc1 TSC complex subunit 1 gene MP:0002047 increased hepatic hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:15888477 733994 Tsc1 TSC complex subunit 1 gene MP:0002049 increased extremity angiosarcoma incidence IAGP N RGD:5509061 20170202 MGI PMID:26777415 733994 Tsc1 TSC complex subunit 1 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:17714952 733994 Tsc1 TSC complex subunit 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20150702 MGI PMID:22763451 733994 Tsc1 TSC complex subunit 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16393152 733994 Tsc1 TSC complex subunit 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:21062901 733994 Tsc1 TSC complex subunit 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:21896734 733994 Tsc1 TSC complex subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11875047 733994 Tsc1 TSC complex subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15601645 733994 Tsc1 TSC complex subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18495876 733994 Tsc1 TSC complex subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21062901 733994 Tsc1 TSC complex subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21896734 733994 Tsc1 TSC complex subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20150507 MGI PMID:23851502 733994 Tsc1 TSC complex subunit 1 gene MP:0002083 premature death IAGP N RGD:5509061 20151224 MGI PMID:23696872 733994 Tsc1 TSC complex subunit 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20151224 MGI PMID:23696872 733994 Tsc1 TSC complex subunit 1 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:18495876 733994 Tsc1 TSC complex subunit 1 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:18568033 733994 Tsc1 TSC complex subunit 1 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:21062901 733994 Tsc1 TSC complex subunit 1 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:11875047 733994 Tsc1 TSC complex subunit 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 733994 Tsc1 TSC complex subunit 1 gene MP:0002546 mydriasis IAGP N RGD:5509061 20190516 MGI PMID:28250050 733994 Tsc1 TSC complex subunit 1 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20150702 MGI PMID:22763451 733994 Tsc1 TSC complex subunit 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20150702 MGI PMID:23250422 733994 Tsc1 TSC complex subunit 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21479224 733994 Tsc1 TSC complex subunit 1 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 733994 Tsc1 TSC complex subunit 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20170202 MGI PMID:26777415 733994 Tsc1 TSC complex subunit 1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15601645 733994 Tsc1 TSC complex subunit 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18495876 733994 Tsc1 TSC complex subunit 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20151224 MGI PMID:23696872 733994 Tsc1 TSC complex subunit 1 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17714952 733994 Tsc1 TSC complex subunit 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:18568033 733994 Tsc1 TSC complex subunit 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21062901 733994 Tsc1 TSC complex subunit 1 gene MP:0003382 straub tail IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:21179166 733994 Tsc1 TSC complex subunit 1 gene MP:0003462 abnormal response to novel odor IAGP N RGD:5509061 20150702 MGI PMID:22763451 733994 Tsc1 TSC complex subunit 1 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:16393152 733994 Tsc1 TSC complex subunit 1 gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:18495876 733994 Tsc1 TSC complex subunit 1 gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0003570 increased uterus leiomyoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0003574 abnormal oviduct morphology IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20150702 MGI PMID:22763451 733994 Tsc1 TSC complex subunit 1 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11875047 733994 Tsc1 TSC complex subunit 1 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20170202 MGI PMID:26777415 733994 Tsc1 TSC complex subunit 1 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:15888477 733994 Tsc1 TSC complex subunit 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11875047 733994 Tsc1 TSC complex subunit 1 gene MP:0003956 abnormal body size IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11875047 733994 Tsc1 TSC complex subunit 1 gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20220609 MGI PMID:28523278 733994 Tsc1 TSC complex subunit 1 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20220609 MGI PMID:28523278 733994 Tsc1 TSC complex subunit 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:18495876 733994 Tsc1 TSC complex subunit 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:21321084 733994 Tsc1 TSC complex subunit 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21321084 733994 Tsc1 TSC complex subunit 1 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20190516 MGI PMID:28250050 733994 Tsc1 TSC complex subunit 1 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20151224 MGI PMID:23696872 733994 Tsc1 TSC complex subunit 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:15601645 733994 Tsc1 TSC complex subunit 1 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20220609 MGI PMID:28523278 733994 Tsc1 TSC complex subunit 1 gene MP:0004682 small intervertebral disk IAGP N RGD:5509061 20220609 MGI PMID:28523278 733994 Tsc1 TSC complex subunit 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22791749 733994 Tsc1 TSC complex subunit 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:22791749 733994 Tsc1 TSC complex subunit 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0004968 kidney epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18724376 733994 Tsc1 TSC complex subunit 1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20190516 MGI PMID:28250050 733994 Tsc1 TSC complex subunit 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15601645 733994 Tsc1 TSC complex subunit 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20151224 MGI PMID:23696872 733994 Tsc1 TSC complex subunit 1 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20190516 MGI PMID:28250050 733994 Tsc1 TSC complex subunit 1 gene MP:0005195 abnormal posterior eye segment morphology IAGP N RGD:5509061 20190516 MGI PMID:28250050 733994 Tsc1 TSC complex subunit 1 gene MP:0005199 abnormal iris pigment epithelium IAGP N RGD:5509061 20190516 MGI PMID:28250050 733994 Tsc1 TSC complex subunit 1 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20190516 MGI PMID:28250050 733994 Tsc1 TSC complex subunit 1 gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20220609 MGI PMID:28523278 733994 Tsc1 TSC complex subunit 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:21062901 733994 Tsc1 TSC complex subunit 1 gene MP:0005238 increased brain size IAGP N RGD:5509061 20151224 MGI PMID:23696872 733994 Tsc1 TSC complex subunit 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21479224 733994 Tsc1 TSC complex subunit 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:11875047 733994 Tsc1 TSC complex subunit 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21479224 733994 Tsc1 TSC complex subunit 1 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20150702 MGI PMID:23250422 733994 Tsc1 TSC complex subunit 1 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:21179166 733994 Tsc1 TSC complex subunit 1 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20170202 MGI PMID:26777415 733994 Tsc1 TSC complex subunit 1 gene MP:0005603 neuron hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18568033 733994 Tsc1 TSC complex subunit 1 gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20190516 MGI PMID:28250050 733994 Tsc1 TSC complex subunit 1 gene MP:0006393 absent nucleus pulposus IAGP N RGD:5509061 20220609 MGI PMID:28523278 733994 Tsc1 TSC complex subunit 1 gene MP:0006432 abnormal costal cartilage morphology IAGP N RGD:5509061 20220609 MGI PMID:28523278 733994 Tsc1 TSC complex subunit 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20170202 MGI PMID:26777415 733994 Tsc1 TSC complex subunit 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18495876 733994 Tsc1 TSC complex subunit 1 gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0008262 abnormal hippocampus region morphology IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21062901 733994 Tsc1 TSC complex subunit 1 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:18724376 733994 Tsc1 TSC complex subunit 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20151224 MGI PMID:23696872 733994 Tsc1 TSC complex subunit 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20150702 MGI PMID:22763451 733994 Tsc1 TSC complex subunit 1 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17714952 733994 Tsc1 TSC complex subunit 1 gene MP:0009012 short diestrus IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0009069 dilated oviduct IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0009092 endometrium hyperplasia IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17522300 733994 Tsc1 TSC complex subunit 1 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21062901 733994 Tsc1 TSC complex subunit 1 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15601645 733994 Tsc1 TSC complex subunit 1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21479224 733994 Tsc1 TSC complex subunit 1 gene MP:0010309 increased mesothelioma incidence IAGP N RGD:5509061 20150507 MGI PMID:23851502 733994 Tsc1 TSC complex subunit 1 gene MP:0010384 increased renal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0010384 increased renal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11875047 733994 Tsc1 TSC complex subunit 1 gene MP:0010384 increased renal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15888477 733994 Tsc1 TSC complex subunit 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18568033 733994 Tsc1 TSC complex subunit 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18724376 733994 Tsc1 TSC complex subunit 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15888477 733994 Tsc1 TSC complex subunit 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23666760 733994 Tsc1 TSC complex subunit 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11438694 733994 Tsc1 TSC complex subunit 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11875047 733994 Tsc1 TSC complex subunit 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15888477 733994 Tsc1 TSC complex subunit 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21321084 733994 Tsc1 TSC complex subunit 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21321084 733994 Tsc1 TSC complex subunit 1 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22791749 733994 Tsc1 TSC complex subunit 1 gene MP:0013140 excessive vocalization IAGP N RGD:5509061 20150702 MGI PMID:22763451 733994 Tsc1 TSC complex subunit 1 gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20150507 MGI PMID:23851502 733994 Tsc1 TSC complex subunit 1 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:21321084 733994 Tsc1 TSC complex subunit 1 gene MP:0014175 abnormal ciliary epithelium morphology IAGP N RGD:5509061 20190516 MGI PMID:28250050 733994 Tsc1 TSC complex subunit 1 gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:22763451 733994 Tsc1 TSC complex subunit 1 gene MP:0021135 abnormal annulus fibrosus morphology IAGP N RGD:5509061 20220609 MGI PMID:28523278 733994 Tsc1 TSC complex subunit 1 gene MP:0021170 spinal stenosis IAGP N RGD:5509061 20220721 MGI PMID:28523278 733994 Tsc1 TSC complex subunit 1 gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20200130 MGI PMID:19843540 733994 Tsc1 TSC complex subunit 1 gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:22128018 733994 Tsc1 TSC complex subunit 1 gene MP:0031407 increased Sertoli cell proliferation IAGP N RGD:5509061 20220630 MGI PMID:22791749 733994 Tsc1 TSC complex subunit 1 gene MP:0031614 fetal cardiomyocyte vacuoles IAGP N RGD:5509061 20240509 MGI PMID:15888477 734003 Prl3d1 prolactin family 3, subfamily d, member 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 734003 Prl3d1 prolactin family 3, subfamily d, member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22516201 734003 Prl3d1 prolactin family 3, subfamily d, member 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 734006 Htr1f 5-hydroxytryptamine (serotonin) receptor 1F gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 734006 Htr1f 5-hydroxytryptamine (serotonin) receptor 1F gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 734006 Htr1f 5-hydroxytryptamine (serotonin) receptor 1F gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20170105 MGI 734006 Htr1f 5-hydroxytryptamine (serotonin) receptor 1F gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20111116 MGI 734006 Htr1f 5-hydroxytryptamine (serotonin) receptor 1F gene MP:0011999 abnormal tail length IEA N RGD:5509061 20201022 MGI 734011 Hsd3b7 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:17601774 734011 Hsd3b7 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 gene MP:0001197 oily skin IAGP N RGD:5509061 20141003 MGI PMID:17601774 734011 Hsd3b7 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17601774 734011 Hsd3b7 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17601774 734011 Hsd3b7 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:17601774 734011 Hsd3b7 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17601774 734011 Hsd3b7 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17601774 734011 Hsd3b7 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17601774 734011 Hsd3b7 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17601774 734011 Hsd3b7 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17601774 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20211021 MGI 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12556476 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:8797826 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15169909 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20160421 MGI 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0001513 limb grasping IEA N RGD:5509061 20160421 MGI 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20141003 MGI 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12556476 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8797826 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0002607 decreased basophil cell number IEA N RGD:5509061 20211021 MGI 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0002644 decreased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8797826 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8797826 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:8797826 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:12556476 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8797826 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12556476 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8797826 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220317 MGI PMID:12784252 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20220317 MGI PMID:12784252 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0008966 abnormal chiasmata formation IAGP N RGD:5509061 20141003 MGI PMID:12556476 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:8797826 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20220317 MGI PMID:12784252 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20220317 MGI PMID:12784252 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20220317 MGI PMID:12556476 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:15169909 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:8797826 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0010207 abnormal telomere morphology IAGP N RGD:5509061 20220317 MGI PMID:12556476 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20141003 MGI PMID:21807948 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15169909 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15169909 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220317 MGI PMID:12556476 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220317 MGI PMID:8797826 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20220317 MGI PMID:12784252 734012 Ube2b ubiquitin-conjugating enzyme E2B gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220317 MGI PMID:12784252 734013 Oat ornithine aminotransferase gene MP:0000377 abnormal hair follicle morphology IEA N RGD:5509061 20141030 MGI 734013 Oat ornithine aminotransferase gene MP:0000420 ruffled hair IEA N RGD:5509061 20141030 MGI 734013 Oat ornithine aminotransferase gene MP:0000424 retarded hair growth IAGP N RGD:5509061 20180712 MGI PMID:25264521 734013 Oat ornithine aminotransferase gene MP:0001265 decreased body size IAGP N RGD:5509061 20180712 MGI PMID:25264521 734013 Oat ornithine aminotransferase gene MP:0001304 cataract IEA N RGD:5509061 20141030 MGI 734013 Oat ornithine aminotransferase gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:10655512 734013 Oat ornithine aminotransferase gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:10655512 734013 Oat ornithine aminotransferase gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:7550347 734013 Oat ornithine aminotransferase gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:7550347 734013 Oat ornithine aminotransferase gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20141030 MGI 734013 Oat ornithine aminotransferase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180705 MGI PMID:25264521 734013 Oat ornithine aminotransferase gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20141030 MGI 734013 Oat ornithine aminotransferase gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10655512 734013 Oat ornithine aminotransferase gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7550347 734013 Oat ornithine aminotransferase gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:7550347 734013 Oat ornithine aminotransferase gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:7550347 734013 Oat ornithine aminotransferase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:10655512 734013 Oat ornithine aminotransferase gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:7550347 734013 Oat ornithine aminotransferase gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20141030 MGI 734013 Oat ornithine aminotransferase gene MP:0005478 decreased circulating thyroxine level IEA N RGD:5509061 20141030 MGI 734013 Oat ornithine aminotransferase gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20180705 MGI PMID:25264521 734013 Oat ornithine aminotransferase gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10655512 734013 Oat ornithine aminotransferase gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:10655512 734013 Oat ornithine aminotransferase gene MP:0008581 disorganized photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:10655512 734013 Oat ornithine aminotransferase gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:10655512 734013 Oat ornithine aminotransferase gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:10655512 734013 Oat ornithine aminotransferase gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:7550347 734013 Oat ornithine aminotransferase gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20180705 MGI PMID:25264521 734013 Oat ornithine aminotransferase gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20141030 MGI 734013 Oat ornithine aminotransferase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7550347 734013 Oat ornithine aminotransferase gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180712 MGI PMID:25264521 734013 Oat ornithine aminotransferase gene MP:0011765 oroticaciduria IAGP N RGD:5509061 20141003 MGI PMID:7550347 734013 Oat ornithine aminotransferase gene MP:0020837 decreased circulating citrulline level IAGP N RGD:5509061 20180712 MGI PMID:7550347 734013 Oat ornithine aminotransferase gene MP:0030650 increased circulating ornithine level IAGP N RGD:5509061 20180913 MGI PMID:25264521 734013 Oat ornithine aminotransferase gene MP:0030650 increased circulating ornithine level IAGP N RGD:5509061 20180913 MGI PMID:7550347 734013 Oat ornithine aminotransferase gene MP:0030651 decreased circulating ornithine level IAGP N RGD:5509061 20180913 MGI PMID:7550347 734013 Oat ornithine aminotransferase gene MP:0030662 decreased circulating arginine level IAGP N RGD:5509061 20180913 MGI PMID:7550347 734013 Oat ornithine aminotransferase gene MP:0030671 decreased circulating phenylalanine level IAGP N RGD:5509061 20180913 MGI PMID:7550347 734015 Cdk16 cyclin dependent kinase 16 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:22184064 734015 Cdk16 cyclin dependent kinase 16 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22184064 734015 Cdk16 cyclin dependent kinase 16 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22184064 734015 Cdk16 cyclin dependent kinase 16 gene MP:0002208 abnormal germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22184064 734015 Cdk16 cyclin dependent kinase 16 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:22184064 734015 Cdk16 cyclin dependent kinase 16 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:22184064 734015 Cdk16 cyclin dependent kinase 16 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:22184064 734015 Cdk16 cyclin dependent kinase 16 gene MP:0009834 abnormal sperm annulus morphology IAGP N RGD:5509061 20141003 MGI PMID:22184064 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20220811 MGI 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20220811 MGI 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20220811 MGI 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0000828 abnormal fourth ventricle morphology IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0001147 small testis IAGP N RGD:5509061 20200820 MGI PMID:31779270 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0001304 cataract IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220811 MGI 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220811 MGI 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20200820 MGI PMID:31779270 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200820 MGI PMID:31779270 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0003202 abnormal neuron apoptosis IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20200820 MGI PMID:31779270 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0006052 cerebellum hemorrhage IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0006308 enlarged seminiferous tubules IAGP N RGD:5509061 20200820 MGI PMID:31779270 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0006418 abnormal testis cord formation IAGP N RGD:5509061 20200820 MGI PMID:31779270 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0006428 ectopic Sertoli cells IAGP N RGD:5509061 20200820 MGI PMID:31779270 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0008794 increased lens epithelium apoptosis IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170209 MGI PMID:17129780 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220811 MGI 734017 Ddb1 damage specific DNA binding protein 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 734020 Cd3d CD3 antigen, delta polypeptide gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9135151 734020 Cd3d CD3 antigen, delta polypeptide gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9135151 734020 Cd3d CD3 antigen, delta polypeptide gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9135151 734026 Stau1 staufen double-stranded RNA binding protein 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18922781 734026 Stau1 staufen double-stranded RNA binding protein 1 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:18922781 734026 Stau1 staufen double-stranded RNA binding protein 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18922781 734030 Hspbp1 HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1 gene MP:0001147 small testis IAGP N RGD:5509061 20150924 MGI PMID:24899640 734030 Hspbp1 HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20150924 MGI PMID:24899640 734030 Hspbp1 HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20150924 MGI PMID:24899640 734030 Hspbp1 HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20150924 MGI PMID:24899640 734030 Hspbp1 HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20150924 MGI PMID:24899640 734030 Hspbp1 HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20150924 MGI PMID:24899640 734030 Hspbp1 HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20150924 MGI PMID:24899640 734030 Hspbp1 HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20150924 MGI PMID:24899640 734030 Hspbp1 HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20150924 MGI PMID:24899640 734030 Hspbp1 HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:24899640 734032 Zp1 zona pellucida glycoprotein 1 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:10433913 734032 Zp1 zona pellucida glycoprotein 1 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:10433913 734032 Zp1 zona pellucida glycoprotein 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10433913 734032 Zp1 zona pellucida glycoprotein 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10433913 734032 Zp1 zona pellucida glycoprotein 1 gene MP:0003696 abnormal zona pellucida morphology IAGP N RGD:5509061 20141003 MGI PMID:10433913 734032 Zp1 zona pellucida glycoprotein 1 gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10433913 734032 Zp1 zona pellucida glycoprotein 1 gene MP:0009375 thin zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:10433913 734033 Stx17 syntaxin 17 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20240314 MGI PMID:36948287 734033 Stx17 syntaxin 17 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20240314 MGI PMID:36948287 734033 Stx17 syntaxin 17 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20240314 MGI PMID:36948287 734033 Stx17 syntaxin 17 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20240314 MGI PMID:36948287 734036 Elp1 elongator complex protein 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:19015235 734036 Elp1 elongator complex protein 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:19015235 734036 Elp1 elongator complex protein 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:19015235 734036 Elp1 elongator complex protein 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0000960 abnormal sensory ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:24173031 734036 Elp1 elongator complex protein 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20190207 MGI PMID:27997532 734036 Elp1 elongator complex protein 1 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20190207 MGI PMID:27997532 734036 Elp1 elongator complex protein 1 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:24173031 734036 Elp1 elongator complex protein 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:24173031 734036 Elp1 elongator complex protein 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20190207 MGI PMID:27997532 734036 Elp1 elongator complex protein 1 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:24173031 734036 Elp1 elongator complex protein 1 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0001017 abnormal stellate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001017 abnormal stellate ganglion morphology IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001059 optic nerve atrophy IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001147 small testis IAGP N RGD:5509061 20230803 MGI PMID:23717213 734036 Elp1 elongator complex protein 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190207 MGI PMID:27997532 734036 Elp1 elongator complex protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190207 MGI PMID:27997532 734036 Elp1 elongator complex protein 1 gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190207 MGI PMID:27997532 734036 Elp1 elongator complex protein 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20190207 MGI PMID:27997532 734036 Elp1 elongator complex protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19015235 734036 Elp1 elongator complex protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:19015235 734036 Elp1 elongator complex protein 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20141003 MGI PMID:19015235 734036 Elp1 elongator complex protein 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:19015235 734036 Elp1 elongator complex protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20190207 MGI PMID:27997532 734036 Elp1 elongator complex protein 1 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20230803 MGI PMID:23717213 734036 Elp1 elongator complex protein 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20190207 MGI PMID:27997532 734036 Elp1 elongator complex protein 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:19015235 734036 Elp1 elongator complex protein 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20190207 MGI PMID:27997532 734036 Elp1 elongator complex protein 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0002980 abnormal postural reflex IAGP N RGD:5509061 20190207 MGI PMID:27997532 734036 Elp1 elongator complex protein 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24173031 734036 Elp1 elongator complex protein 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19015235 734036 Elp1 elongator complex protein 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0003289 abnormal intestinal peristalsis IAGP N RGD:5509061 20190207 MGI PMID:27997532 734036 Elp1 elongator complex protein 1 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:24173031 734036 Elp1 elongator complex protein 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:24173031 734036 Elp1 elongator complex protein 1 gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20141003 MGI PMID:24173031 734036 Elp1 elongator complex protein 1 gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20141003 MGI PMID:19015235 734036 Elp1 elongator complex protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:24173031 734036 Elp1 elongator complex protein 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:19015235 734036 Elp1 elongator complex protein 1 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:19015235 734036 Elp1 elongator complex protein 1 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0004259 small placenta IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0004573 absent limb buds IAGP N RGD:5509061 20141003 MGI PMID:19015235 734036 Elp1 elongator complex protein 1 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20230803 MGI PMID:23717213 734036 Elp1 elongator complex protein 1 gene MP:0005302 neurogenic bladder IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0006222 optic neuropathy IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0006257 abnormal fungiform papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0006257 abnormal fungiform papillae morphology IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0006260 abnormal gustatory papilla taste bud morphology IAGP N RGD:5509061 20230601 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0006276 abnormal autonomic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0006294 absent optic vesicle IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0006404 abnormal lumbar dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0006404 abnormal lumbar dorsal root ganglion morphology IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0008259 abnormal optic disk morphology IAGP N RGD:5509061 20190411 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20230803 MGI PMID:23717213 734036 Elp1 elongator complex protein 1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20190207 MGI PMID:27997532 734036 Elp1 elongator complex protein 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0008492 dorsal root ganglion degeneration IAGP N RGD:5509061 20190207 MGI PMID:27997532 734036 Elp1 elongator complex protein 1 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:24173031 734036 Elp1 elongator complex protein 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:24173031 734036 Elp1 elongator complex protein 1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20230803 MGI PMID:23717213 734036 Elp1 elongator complex protein 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0009561 superior cervical ganglion degeneration IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:24173031 734036 Elp1 elongator complex protein 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20160922 MGI PMID:26769677 734036 Elp1 elongator complex protein 1 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0010382 abnormal dosage compensation, by inactivation of X chromosome IAGP N RGD:5509061 20230803 MGI PMID:23717213 734036 Elp1 elongator complex protein 1 gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20230803 MGI PMID:23717213 734036 Elp1 elongator complex protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24173031 734036 Elp1 elongator complex protein 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22922231 734036 Elp1 elongator complex protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19015235 734036 Elp1 elongator complex protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 734036 Elp1 elongator complex protein 1 gene MP:0011751 abnormal X-Y chromosome synapsis during male meiosis IAGP N RGD:5509061 20230803 MGI PMID:23717213 734036 Elp1 elongator complex protein 1 gene MP:0012541 absent lamina terminalis IAGP N RGD:5509061 20141003 MGI PMID:22046433 734036 Elp1 elongator complex protein 1 gene MP:0030273 mandibular retrognathia IAGP N RGD:5509061 20171026 MGI PMID:24173031 734038 Calcb calcitonin-related polypeptide, beta gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 734038 Calcb calcitonin-related polypeptide, beta gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 734038 Calcb calcitonin-related polypeptide, beta gene MP:0000955 abnormal spinal cord morphology IEA N RGD:5509061 20210128 MGI 734038 Calcb calcitonin-related polypeptide, beta gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20181227 MGI 734038 Calcb calcitonin-related polypeptide, beta gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 734038 Calcb calcitonin-related polypeptide, beta gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20181227 MGI 734038 Calcb calcitonin-related polypeptide, beta gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20181227 MGI 734041 Mcf2l mcf.2 transforming sequence-like gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20141003 MGI 734041 Mcf2l mcf.2 transforming sequence-like gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 734050 Zkscan14 zinc finger with KRAB and SCAN domains 14 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 734050 Zkscan14 zinc finger with KRAB and SCAN domains 14 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18779779 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17332431 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:17332431 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20201022 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11733538 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:11733538 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220811 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16847341 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16847341 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16843452 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17332431 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:18779779 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18779779 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20201022 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:7650482 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10670582 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:10714686 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:11733538 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:11733538 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:16843452 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:17332431 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16843452 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:11733538 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17332431 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16847341 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:16357364 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20201022 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0003184 increased angiotensin I-converting enzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16843452 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16847341 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0003332 liver abscess IAGP N RGD:5509061 20141003 MGI PMID:11733538 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:16843452 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24185898 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0003561 rheumatoid arthritis IAGP N RGD:5509061 20141003 MGI PMID:15310853 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0003604 single kidney IEA N RGD:5509061 20210826 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23426181 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:15310853 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15743827 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:15310853 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:15310853 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:18779779 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:7650482 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0005074 impaired granulocyte bactericidal activity IAGP N RGD:5509061 20141003 MGI PMID:10670582 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:16864727 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:7650482 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0005340 abnormal susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19684185 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:16843452 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:15310853 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16864727 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0006278 aortic aneurysm IAGP N RGD:5509061 20141003 MGI PMID:16864727 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0008725 increased heart atrium size IEA N RGD:5509061 20210826 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16847341 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:7650482 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20230504 MGI PMID:35788118 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0009868 abnormal descending thoracic aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16864727 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 734055 Ncf1 neutrophil cytosolic factor 1 gene MP:0020947 decreased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:18423196 734059 Trpc1 transient receptor potential cation channel, subfamily C, member 1 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:17956991 734059 Trpc1 transient receptor potential cation channel, subfamily C, member 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17647013 734059 Trpc1 transient receptor potential cation channel, subfamily C, member 1 gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:17647013 734059 Trpc1 transient receptor potential cation channel, subfamily C, member 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20210128 MGI 734059 Trpc1 transient receptor potential cation channel, subfamily C, member 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 734059 Trpc1 transient receptor potential cation channel, subfamily C, member 1 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:23188715 734059 Trpc1 transient receptor potential cation channel, subfamily C, member 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 734059 Trpc1 transient receptor potential cation channel, subfamily C, member 1 gene MP:0013300 abnormal submandibular gland physiology IAGP N RGD:5509061 20141225 MGI PMID:17956991 734066 Rcvrn recoverin gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:15882641 734066 Rcvrn recoverin gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15173221 734066 Rcvrn recoverin gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15882641 734068 Fzd9 frizzled class receptor 9 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:21402791 734068 Fzd9 frizzled class receptor 9 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:21402791 734068 Fzd9 frizzled class receptor 9 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:21402791 734068 Fzd9 frizzled class receptor 9 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15572594 734068 Fzd9 frizzled class receptor 9 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15572594 734068 Fzd9 frizzled class receptor 9 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15572594 734068 Fzd9 frizzled class receptor 9 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15572594 734068 Fzd9 frizzled class receptor 9 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15572594 734068 Fzd9 frizzled class receptor 9 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:15930120 734068 Fzd9 frizzled class receptor 9 gene MP:0001258 decreased body length IEA N RGD:5509061 20111116 MGI 734068 Fzd9 frizzled class receptor 9 gene MP:0001262 decreased body weight IEA N RGD:5509061 20111116 MGI 734068 Fzd9 frizzled class receptor 9 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15930120 734068 Fzd9 frizzled class receptor 9 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:21402791 734068 Fzd9 frizzled class receptor 9 gene MP:0001732 postnatal growth retardation IEA N RGD:5509061 20111116 MGI 734068 Fzd9 frizzled class receptor 9 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15572594 734068 Fzd9 frizzled class receptor 9 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:21402791 734068 Fzd9 frizzled class receptor 9 gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:15572594 734068 Fzd9 frizzled class receptor 9 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:15572594 734068 Fzd9 frizzled class receptor 9 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15572594 734068 Fzd9 frizzled class receptor 9 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:15930120 734068 Fzd9 frizzled class receptor 9 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:15930120 734068 Fzd9 frizzled class receptor 9 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:15572594 734068 Fzd9 frizzled class receptor 9 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20111116 MGI 734068 Fzd9 frizzled class receptor 9 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:21402791 734068 Fzd9 frizzled class receptor 9 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:21402791 734068 Fzd9 frizzled class receptor 9 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15572594 734068 Fzd9 frizzled class receptor 9 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15572594 734068 Fzd9 frizzled class receptor 9 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15572594 734068 Fzd9 frizzled class receptor 9 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:15572594 734068 Fzd9 frizzled class receptor 9 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21402791 734068 Fzd9 frizzled class receptor 9 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:21402791 734068 Fzd9 frizzled class receptor 9 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:21402791 734068 Fzd9 frizzled class receptor 9 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:21402791 734068 Fzd9 frizzled class receptor 9 gene MP:0011224 abnormal lymph node medullary cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15572594 734068 Fzd9 frizzled class receptor 9 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:21402791 734068 Fzd9 frizzled class receptor 9 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:21402791 734068 Fzd9 frizzled class receptor 9 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:21402791 734068 Fzd9 frizzled class receptor 9 gene MP:0030439 decreased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:21402791 734072 Atp5po ATP synthase peripheral stalk subunit OSCP gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20230720 MGI 734072 Atp5po ATP synthase peripheral stalk subunit OSCP gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230720 MGI 734072 Atp5po ATP synthase peripheral stalk subunit OSCP gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230720 MGI 734072 Atp5po ATP synthase peripheral stalk subunit OSCP gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230720 MGI 734074 Ugdh UDP-glucose dehydrogenase gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22745308 734074 Ugdh UDP-glucose dehydrogenase gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20141003 MGI PMID:22745308 734074 Ugdh UDP-glucose dehydrogenase gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:14505572 734074 Ugdh UDP-glucose dehydrogenase gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:14505572 734074 Ugdh UDP-glucose dehydrogenase gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15755804 734074 Ugdh UDP-glucose dehydrogenase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22745308 734074 Ugdh UDP-glucose dehydrogenase gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:15755804 734074 Ugdh UDP-glucose dehydrogenase gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14505572 734074 Ugdh UDP-glucose dehydrogenase gene MP:0006323 abnormal extraembryonic mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:14505572 734074 Ugdh UDP-glucose dehydrogenase gene MP:0008932 abnormal embryonic tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:22745308 734074 Ugdh UDP-glucose dehydrogenase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22745308 734074 Ugdh UDP-glucose dehydrogenase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14505572 734074 Ugdh UDP-glucose dehydrogenase gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 734074 Ugdh UDP-glucose dehydrogenase gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:14505572 734074 Ugdh UDP-glucose dehydrogenase gene MP:0013331 abnormal lacrimal gland development IAGP N RGD:5509061 20141204 MGI PMID:22745308 734075 Srcin1 SRC kinase signaling inhibitor 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20151022 MGI PMID:24453341 734075 Srcin1 SRC kinase signaling inhibitor 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20151022 MGI PMID:24453341 734075 Srcin1 SRC kinase signaling inhibitor 1 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20151022 MGI PMID:24453341 734075 Srcin1 SRC kinase signaling inhibitor 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20151022 MGI PMID:24453341 734075 Srcin1 SRC kinase signaling inhibitor 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20151022 MGI PMID:24453341 734075 Srcin1 SRC kinase signaling inhibitor 1 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20151022 MGI PMID:24453341 734075 Srcin1 SRC kinase signaling inhibitor 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20170105 MGI 734075 Srcin1 SRC kinase signaling inhibitor 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20151022 MGI PMID:24453341 734075 Srcin1 SRC kinase signaling inhibitor 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20151022 MGI PMID:24453341 734075 Srcin1 SRC kinase signaling inhibitor 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20230511 MGI PMID:35876795 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:19145245 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20230511 MGI PMID:35876795 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20230511 MGI PMID:35876795 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11385474 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12429860 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17785453 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19145245 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11385474 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11385474 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11385474 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12429860 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17785453 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19145245 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19805137 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20230511 MGI PMID:35876795 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11385474 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:19145245 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19145245 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:17785453 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12429860 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19805137 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19145245 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20230511 MGI PMID:35876795 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17785453 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17785453 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19805137 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:19145245 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11385474 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12429860 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19805137 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20230511 MGI PMID:35876795 734077 Pold1 polymerase (DNA directed), delta 1, catalytic subunit gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20230511 MGI PMID:35876795 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0000226 abnormal mean corpuscular volume IAGP N RGD:5509061 20180719 MGI PMID:9242562 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0001577 anemia IAGP N RGD:5509061 20180719 MGI PMID:12458204 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0001577 anemia IAGP N RGD:5509061 20180719 MGI PMID:8781443 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20180719 MGI PMID:8781443 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0001588 abnormal hemoglobin IAGP N RGD:5509061 20180719 MGI PMID:12458204 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0001588 abnormal hemoglobin IAGP N RGD:5509061 20180719 MGI PMID:8781443 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0001588 abnormal hemoglobin IAGP N RGD:5509061 20180719 MGI PMID:9242562 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0001589 abnormal mean corpuscular hemoglobin IAGP N RGD:5509061 20180719 MGI PMID:9242562 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0002319 hyperoxia IAGP N RGD:5509061 20180719 MGI PMID:12458204 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20180719 MGI PMID:8781443 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20180719 MGI PMID:9242562 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20180719 MGI PMID:8781443 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20180719 MGI PMID:8781443 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20180719 MGI PMID:8781443 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20180719 MGI PMID:9242562 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20180719 MGI PMID:8781443 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20180719 MGI PMID:9242562 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20180719 MGI PMID:8781443 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0003060 increased aerobic running capacity IAGP N RGD:5509061 20180719 MGI PMID:12458204 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0003717 pallor IAGP N RGD:5509061 20180719 MGI PMID:8781443 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20180719 MGI PMID:8781443 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20180719 MGI PMID:8781443 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20180719 MGI PMID:9242562 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20180719 MGI PMID:12458204 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20180719 MGI PMID:9242562 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20180719 MGI PMID:8781443 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20180719 MGI PMID:12458204 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20180719 MGI PMID:12458204 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0010175 leptocytosis IAGP N RGD:5509061 20180719 MGI PMID:8781443 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20180719 MGI PMID:12458204 734079 Hba-a1 hemoglobin alpha, adult chain 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:8781443 734081 Cyth2 cytohesin 2 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20220721 MGI PMID:33393815 734081 Cyth2 cytohesin 2 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20220721 MGI PMID:33393815 734081 Cyth2 cytohesin 2 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20180503 MGI PMID:25824033 734084 Rtn4r reticulon 4 receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18043741 734084 Rtn4r reticulon 4 receptor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15504325 734084 Rtn4r reticulon 4 receptor gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:15504325 734084 Rtn4r reticulon 4 receptor gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:21645550 734084 Rtn4r reticulon 4 receptor gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:21645550 734084 Rtn4r reticulon 4 receptor gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:18043741 734084 Rtn4r reticulon 4 receptor gene MP:0003075 abnormal response to CNS ischemic injury IAGP N RGD:5509061 20141003 MGI PMID:21057507 734084 Rtn4r reticulon 4 receptor gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:18411262 734084 Rtn4r reticulon 4 receptor gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22406547 734084 Rtn4r reticulon 4 receptor gene MP:0004858 abnormal nervous system regeneration IAGP N RGD:5509061 20141003 MGI PMID:22162062 734084 Rtn4r reticulon 4 receptor gene MP:0005237 abnormal olfactory tract morphology IAGP N RGD:5509061 20141003 MGI PMID:21817055 734084 Rtn4r reticulon 4 receptor gene MP:0030013 enhanced central nervous system regeneration IAGP N RGD:5509061 20170713 MGI PMID:15504325 734084 Rtn4r reticulon 4 receptor gene MP:0030013 enhanced central nervous system regeneration IAGP N RGD:5509061 20170713 MGI PMID:22406547 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20201022 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20210128 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0001718 abnormal visceral yolk sac morphology IEA N RGD:5509061 20200514 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20200514 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0002884 abnormal pharyngeal arch morphology IEA N RGD:5509061 20201022 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0003229 abnormal vitelline vasculature morphology IEA N RGD:5509061 20220519 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20200514 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20200514 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20200514 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20200514 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20230504 MGI PMID:31422819 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 734092 Got2 glutamatic-oxaloacetic transaminase 2, mitochondrial gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 734094 Xab2 XPA binding protein 2 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:15725628 734094 Xab2 XPA binding protein 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15725628 734094 Xab2 XPA binding protein 2 gene MP:0012111 failure of morula compaction IAGP N RGD:5509061 20141003 MGI PMID:15725628 734097 Lpar3 lysophosphatidic acid receptor 3 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:15875025 734097 Lpar3 lysophosphatidic acid receptor 3 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:15875025 734097 Lpar3 lysophosphatidic acid receptor 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15875025 734097 Lpar3 lysophosphatidic acid receptor 3 gene MP:0002293 long gestation period IAGP N RGD:5509061 20141003 MGI PMID:15875025 734097 Lpar3 lysophosphatidic acid receptor 3 gene MP:0009352 impaired spacing of implantation sites IAGP N RGD:5509061 20141003 MGI PMID:15875025 734097 Lpar3 lysophosphatidic acid receptor 3 gene MP:0009649 delayed embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:15875025 734097 Lpar3 lysophosphatidic acid receptor 3 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:15875025 734099 Emb embigin gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20181227 MGI 734099 Emb embigin gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20240328 MGI PMID:38318368 734099 Emb embigin gene MP:0003641 small lung IAGP N RGD:5509061 20240328 MGI PMID:38318368 734099 Emb embigin gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20240328 MGI PMID:38318368 734099 Emb embigin gene MP:0010811 decreased type II pneumocyte number IAGP N RGD:5509061 20240328 MGI PMID:38318368 734099 Emb embigin gene MP:0010813 abnormal alveolar lamellar body morphology IAGP N RGD:5509061 20240328 MGI PMID:38318368 734099 Emb embigin gene MP:0010816 decreased type I pneumocyte number IAGP N RGD:5509061 20240328 MGI PMID:38318368 734099 Emb embigin gene MP:0010865 prenatal growth retardation IAGP N RGD:5509061 20240328 MGI PMID:38318368 734099 Emb embigin gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20240328 MGI PMID:38318368 734099 Emb embigin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20240328 MGI PMID:38318368 734099 Emb embigin gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20240328 MGI PMID:38318368 734099 Emb embigin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 734099 Emb embigin gene MP:0011585 decreased alkaline phosphatase activity IAGP N RGD:5509061 20240328 MGI PMID:38318368 734099 Emb embigin gene MP:0012172 abnormal amniotic fluid composition IAGP N RGD:5509061 20240328 MGI PMID:38318368 734101 Rab14 RAB14, member RAS oncogene family gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20240502 MGI PMID:36379959 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11030617 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17283114 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:17183066 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:17283114 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19815629 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17183066 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11030617 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17720959 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18820241 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:17283114 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:17283114 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:11030617 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18820241 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17183066 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0003324 increased liver adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17283114 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17183066 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17283114 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17183066 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17283114 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19815629 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17183066 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19815629 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:11030617 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20141003 MGI PMID:12917447 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:12917447 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:17720959 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:11030617 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:12917447 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:17183066 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:17283114 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:17720959 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:19815629 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0004789 increased bile salt level IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:11030617 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11030617 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17720959 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18820241 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17283114 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18820241 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11030617 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12917447 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17720959 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:11030617 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17183066 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17283114 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0008988 abnormal liver perisinusoidal space morphology IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0009342 enlarged gallbladder IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11030617 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12917447 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11030617 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11030617 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:11030617 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:23700488 734104 Nr1h4 nuclear receptor subfamily 1, group H, member 4 gene MP:0031236 increased cecum weight IAGP N RGD:5509061 20210610 MGI PMID:23700488 734105 Clrn1 clarin 1 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:19414487 734105 Clrn1 clarin 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 734105 Clrn1 clarin 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 734105 Clrn1 clarin 1 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20210128 MGI 734105 Clrn1 clarin 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:19414487 734105 Clrn1 clarin 1 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200402 MGI 734105 Clrn1 clarin 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:19414487 734105 Clrn1 clarin 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:19414487 734105 Clrn1 clarin 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:22787034 734105 Clrn1 clarin 1 gene MP:0001967 deafness IAGP N RGD:5509061 20181011 MGI PMID:27110679 734105 Clrn1 clarin 1 gene MP:0001967 deafness IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 734105 Clrn1 clarin 1 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20160114 MGI 734105 Clrn1 clarin 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 734105 Clrn1 clarin 1 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0004397 absent cochlear inner hair cells IAGP N RGD:5509061 20141003 MGI PMID:19414487 734105 Clrn1 clarin 1 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0004403 absent cochlear outer hair cells IAGP N RGD:5509061 20141003 MGI PMID:19414487 734105 Clrn1 clarin 1 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0004414 decreased cochlear microphonics IAGP N RGD:5509061 20141003 MGI PMID:22787034 734105 Clrn1 clarin 1 gene MP:0004415 abnormal cochlear nerve compound action potential IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0004432 abnormal cochlear hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22787034 734105 Clrn1 clarin 1 gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0004438 abnormal vestibular hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22787034 734105 Clrn1 clarin 1 gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:19414487 734105 Clrn1 clarin 1 gene MP:0004491 abnormal orientation of outer hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:19414487 734105 Clrn1 clarin 1 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:22787034 734105 Clrn1 clarin 1 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:19414487 734105 Clrn1 clarin 1 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20180531 MGI PMID:29044151 734105 Clrn1 clarin 1 gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20180531 MGI PMID:29044151 734105 Clrn1 clarin 1 gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0004716 abnormal cochlear nerve morphology IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:19414487 734105 Clrn1 clarin 1 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 734105 Clrn1 clarin 1 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0004746 abnormal cochlear IHC afferent innervation pattern IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0004814 reduced linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:19414487 734105 Clrn1 clarin 1 gene MP:0006324 abnormal cochlear nerve fiber response IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:19414487 734105 Clrn1 clarin 1 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20180531 MGI PMID:29044151 734105 Clrn1 clarin 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:19414487 734105 Clrn1 clarin 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:19414487 734105 Clrn1 clarin 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:22787034 734105 Clrn1 clarin 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20181011 MGI PMID:27110679 734105 Clrn1 clarin 1 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0020359 abnormal ribbon synapse morphology IAGP N RGD:5509061 20201029 MGI PMID:29985171 734105 Clrn1 clarin 1 gene MP:0030950 abnormal synaptic vesicle exocytosis IAGP N RGD:5509061 20201029 MGI PMID:29985171 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0000746 weakness IEA N RGD:5509061 20111116 MGI 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:18206390 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:11414794 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11414794 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15321743 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15706241 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20111116 MGI 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18206390 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0001429 dehydration IEA N RGD:5509061 20111116 MGI 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:16701209 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16701209 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:11498050 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:19246384 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0001504 abnormal posture IEA N RGD:5509061 20111116 MGI 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:16682806 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15493018 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:16682806 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:16682806 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11498050 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:19246384 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11414794 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11498050 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:15706241 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18206390 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11498050 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:18206390 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:16928868 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:11498050 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16701209 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20191031 MGI PMID:30902970 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002911 abnormal inhibitory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:11414794 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:11498050 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16701209 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19246384 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:11498050 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11498050 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:18206390 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:11498050 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:11414794 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:11498050 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11498050 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:18206390 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:11498050 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22993424 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0005124 increased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:16682806 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:11414794 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:18206390 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:18206390 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0006404 abnormal lumbar dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18206390 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0008843 absent subcutaneous adipose tissue IEA N RGD:5509061 20111116 MGI 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11498050 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0009015 short proestrus IAGP N RGD:5509061 20141003 MGI PMID:16682806 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20141003 MGI PMID:16682806 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:11414794 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11498050 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15321743 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11414794 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11431694 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20141003 MGI PMID:22993424 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0014413 decreased depression-related behavior IAGP N RGD:5509061 20240425 MGI PMID:15706241 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:11498050 734109 Gabbr1 gamma-aminobutyric acid type B receptor subunit 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:15493018 734110 Dffa DNA fragmentation factor, alpha subunit gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:10837799 734110 Dffa DNA fragmentation factor, alpha subunit gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10837799 734110 Dffa DNA fragmentation factor, alpha subunit gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14663139 734110 Dffa DNA fragmentation factor, alpha subunit gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9770511 734110 Dffa DNA fragmentation factor, alpha subunit gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14663139 734110 Dffa DNA fragmentation factor, alpha subunit gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11478773 734111 Pbsn probasin gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20240523 MGI 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:11823606 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0001355 submission towards male mice IAGP N RGD:5509061 20141003 MGI PMID:11823606 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0001355 submission towards male mice IAGP N RGD:5509061 20141003 MGI PMID:11972034 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0001375 abnormal mating preference IAGP N RGD:5509061 20141003 MGI PMID:11823606 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0001375 abnormal mating preference IAGP N RGD:5509061 20141003 MGI PMID:11972034 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20111116 MGI 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20161222 MGI PMID:27916458 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20161222 MGI PMID:27916458 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20210520 MGI 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0002243 abnormal vomeronasal organ morphology IAGP N RGD:5509061 20141003 MGI PMID:11823606 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11823606 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11972034 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:20596023 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:21924222 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:21924222 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21924222 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:11972034 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20191226 MGI PMID:31653840 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20111116 MGI 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:21924222 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0009945 abnormal accessory olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:11823606 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0011176 abnormal erythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:21924222 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20161222 MGI PMID:27916458 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0011678 abnormal vomeronasal sensory neuron physiology IAGP N RGD:5509061 20191226 MGI PMID:31653840 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0031252 abnormal physiological response to hypoxia IAGP N RGD:5509061 20210805 MGI PMID:27916458 734117 Trpc2 transient receptor potential cation channel, subfamily C, member 2 gene MP:0031252 abnormal physiological response to hypoxia IAGP N RGD:5509061 20210805 MGI PMID:34186026 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000018 small ears IEA N RGD:5509061 20141003 MGI 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000084 abnormal fontanelle morphology IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000098 abnormal vomer bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14610065 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:12952213 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:14610065 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14610065 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:20858856 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:20727881 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000736 delayed muscle development IAGP N RGD:5509061 20141003 MGI PMID:15064723 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15064723 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:15064723 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:15572153 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15739229 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:15572153 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:15739229 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15064723 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20727881 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001296 macrophthalmia IEA N RGD:5509061 20111116 MGI 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001406 abnormal gait IEA N RGD:5509061 20141003 MGI 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:16926191 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:14610065 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15064723 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15064723 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20858856 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:20858856 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0001924 infertility IEA N RGD:5509061 20111116 MGI 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20727881 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16926191 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002089 abnormal postnatal growth/weight/body size IEA N RGD:5509061 20111116 MGI 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:20727881 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15064723 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:15572153 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002268 abnormal terminal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:15739229 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:15572153 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:15739229 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18762577 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002750 exophthalmos IEA N RGD:5509061 20141003 MGI 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:14610065 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:16926191 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:20727881 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:14610065 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003053 delayed tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:12952213 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16926191 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20727881 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15739229 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003379 absent sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:20858856 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:15572153 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003851 skeletal muscle interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16926191 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20858856 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:20727881 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:20727881 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0004420 parietal bone hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0004455 pterygoid bone hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:20727881 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:12952213 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0004830 short incisors IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:20727881 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:20858856 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:12952213 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0005458 increased percent body fat/body weight IEA N RGD:5509061 20141003 MGI 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15064723 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:14610065 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:15739229 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15064723 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0008525 decreased cranium height IEA N RGD:5509061 20111116 MGI 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0008526 decreased cranium width IEA N RGD:5509061 20141003 MGI 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0008529 enlarged optic nerve IEA N RGD:5509061 20141003 MGI 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20858856 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:16926191 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:16926191 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141218 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0009520 decreased submandibular gland size IAGP N RGD:5509061 20141003 MGI PMID:15572153 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:15064723 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0009900 vomer bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20141218 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0010030 abnormal orbit morphology IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0010809 abnormal club cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15739229 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:15739229 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0010870 absent bone trabeculae IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0010905 absent alveolar pores IAGP N RGD:5509061 20141003 MGI PMID:15739229 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0010908 dilated pulmonary alveolar duct IAGP N RGD:5509061 20141003 MGI PMID:15739229 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15572153 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10520996 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15064723 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20858856 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011156 abnormal hypodermis fat layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011360 kidney cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20727881 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011376 abnormal kidney corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:20727881 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20727881 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20170907 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0011967 increased or absent threshold for auditory brainstem response IEA N RGD:5509061 20141003 MGI 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0013542 abnormal submandibular gland branching morphogenesis IAGP N RGD:5509061 20150226 MGI PMID:15572153 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0030009 increased bone marrow adipose tissue amount IAGP N RGD:5509061 20170706 MGI PMID:23685250 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0030077 small cranial cavity IAGP N RGD:5509061 20170928 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0030089 short lower incisors IAGP N RGD:5509061 20170928 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0030090 short upper incisors IAGP N RGD:5509061 20170928 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20170928 MGI PMID:18022611 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0030137 abnormal upper incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0030225 abnormal cranial vertex morphology IAGP N RGD:5509061 20171019 MGI PMID:10737763 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0030245 round head IEA N RGD:5509061 20171019 MGI 734119 Mmp14 matrix metallopeptidase 14 (membrane-inserted) gene MP:0030279 thin neurocranium IAGP N RGD:5509061 20171102 MGI PMID:18022611 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20171123 MGI PMID:11823447 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:12149478 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15750185 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:12149478 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15615595 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:15750185 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:15750185 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000486 abnormal pulmonary trunk morphology IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000508 right-sided isomerism IAGP N RGD:5509061 20141003 MGI PMID:15750185 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:17615577 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:15750185 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:18358466 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000650 mesocardia IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:11823447 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12149478 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17133411 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11823447 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:11823447 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:11823447 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:18358466 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12149478 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17133411 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15750185 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:11823447 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17133411 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17133411 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23082118 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:17133411 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:18358466 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18358466 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0002274 abnormal type I pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18358466 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18358466 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:12149478 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15615595 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:15615595 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:11823447 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:15750185 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:18358466 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:11823447 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23082118 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20141003 MGI PMID:15615595 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0005313 absent adrenal gland IAGP N RGD:5509061 20141003 MGI PMID:23082118 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:18358466 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0006046 atrioventricular valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:12149478 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:15750185 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:23082118 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0006063 abnormal inferior vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0006063 abnormal inferior vena cava morphology IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:15615595 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0009688 abnormal spinal cord central canal morphology IAGP N RGD:5509061 20141003 MGI PMID:12149478 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20171123 MGI PMID:15750185 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11823447 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12149478 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15615595 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23082118 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:15615595 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:23082118 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010426 abnormal heart and great artery attachment IAGP N RGD:5509061 20141003 MGI PMID:12149478 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010437 absent coronary sinus IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:11823447 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010457 pulmonary artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:12149478 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010466 vascular ring IAGP N RGD:5509061 20141003 MGI PMID:15615595 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:15475956 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010714 iris coloboma IAGP N RGD:5509061 20141003 MGI PMID:12149478 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010807 abnormal stomach position or orientation IAGP N RGD:5509061 20141003 MGI PMID:15750185 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010814 absent alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:18358466 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0010976 small lung lobe IAGP N RGD:5509061 20141003 MGI PMID:18358466 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17615577 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11823447 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12149478 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12149478 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17615577 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18440989 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20171123 MGI PMID:11823447 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0012747 abnormal cardiac neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0012749 decreased cardiac neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0012750 absent cardiac neural crest cells IAGP N RGD:5509061 20141003 MGI PMID:11694877 734121 Cited2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 gene MP:0013176 abnormal tail position or orientation IAGP N RGD:5509061 20141003 MGI PMID:15475956 734124 Padi1 peptidyl arginine deiminase, type I gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 734124 Padi1 peptidyl arginine deiminase, type I gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11442353 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:18604572 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:6949984 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18604572 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:6949984 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:6949984 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001393 ataxia IEA N RGD:5509061 20141003 MGI 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11442353 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:6949984 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:11442353 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16467533 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16467533 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16467533 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16467533 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001505 hunched posture IEA N RGD:5509061 20111116 MGI 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20111116 MGI 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:11442353 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:11442353 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:6949984 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:18604572 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:6949984 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15190101 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:16467533 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0002566 abnormal sexual interaction IEA N RGD:5509061 20111116 MGI 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:11442353 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0002800 abnormal short-term object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:11442353 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:16467533 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:6949984 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20141003 MGI PMID:15190101 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20141003 MGI PMID:18604572 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:18604572 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0003492 abnormal involuntary movement IEA N RGD:5509061 20141003 MGI 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:22554781 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0008026 abnormal brain white matter morphology IEA N RGD:5509061 20111124 MGI 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0008027 abnormal spinal cord white matter morphology IEA N RGD:5509061 20111124 MGI 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18604572 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6949984 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16467533 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20141127 MGI 734126 Kcnn2 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6949984 734128 Cep78 centrosomal protein 78 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0001925 male infertility IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0001925 male infertility IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0002660 abnormal caput epididymis morphology IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0004085 abnormal heartbeat IEA N RGD:5509061 20220519 MGI 734128 Cep78 centrosomal protein 78 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0008545 absent sperm flagellum IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0009239 short sperm flagellum IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0009839 multiflagellated sperm IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20230330 MGI PMID:36206347 734128 Cep78 centrosomal protein 78 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0031373 abnormal manchette perinuclear ring morphology IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0031374 abnormal manchette assembly IAGP N RGD:5509061 20230622 MGI PMID:36756949 734128 Cep78 centrosomal protein 78 gene MP:0031386 elongated manchette IAGP N RGD:5509061 20230622 MGI PMID:36756949 734129 Hsd17b12 hydroxysteroid (17-beta) dehydrogenase 12 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20130115 734129 Hsd17b12 hydroxysteroid (17-beta) dehydrogenase 12 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20130115 734129 Hsd17b12 hydroxysteroid (17-beta) dehydrogenase 12 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:20130115 734129 Hsd17b12 hydroxysteroid (17-beta) dehydrogenase 12 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:20130115 734129 Hsd17b12 hydroxysteroid (17-beta) dehydrogenase 12 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:20130115 734129 Hsd17b12 hydroxysteroid (17-beta) dehydrogenase 12 gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20130115 734129 Hsd17b12 hydroxysteroid (17-beta) dehydrogenase 12 gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:20130115 734129 Hsd17b12 hydroxysteroid (17-beta) dehydrogenase 12 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20130115 734129 Hsd17b12 hydroxysteroid (17-beta) dehydrogenase 12 gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:20130115 734129 Hsd17b12 hydroxysteroid (17-beta) dehydrogenase 12 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20130115 734129 Hsd17b12 hydroxysteroid (17-beta) dehydrogenase 12 gene MP:0006386 absent somites IAGP N RGD:5509061 20141003 MGI PMID:20130115 734129 Hsd17b12 hydroxysteroid (17-beta) dehydrogenase 12 gene MP:0009593 absent chorion IAGP N RGD:5509061 20141003 MGI PMID:20130115 734129 Hsd17b12 hydroxysteroid (17-beta) dehydrogenase 12 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20130115 734129 Hsd17b12 hydroxysteroid (17-beta) dehydrogenase 12 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:20130115 734131 Faim Fas apoptotic inhibitory molecule gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:19300454 734131 Faim Fas apoptotic inhibitory molecule gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:19300454 734131 Faim Fas apoptotic inhibitory molecule gene MP:0003326 liver failure IAGP N RGD:5509061 20141003 MGI PMID:19300454 734131 Faim Fas apoptotic inhibitory molecule gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19300454 734131 Faim Fas apoptotic inhibitory molecule gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19300454 734131 Faim Fas apoptotic inhibitory molecule gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19300454 734131 Faim Fas apoptotic inhibitory molecule gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19300454 734131 Faim Fas apoptotic inhibitory molecule gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19300454 734134 Ncdn neurochondrin gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:14559245 734134 Ncdn neurochondrin gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:14559245 734134 Ncdn neurochondrin gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14559245 734134 Ncdn neurochondrin gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:15790563 734134 Ncdn neurochondrin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15790563 734134 Ncdn neurochondrin gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15790563 734134 Ncdn neurochondrin gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:20007903 734134 Ncdn neurochondrin gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:20007903 734134 Ncdn neurochondrin gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:14559245 734134 Ncdn neurochondrin gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15790563 734134 Ncdn neurochondrin gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15790563 734134 Ncdn neurochondrin gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15790563 734134 Ncdn neurochondrin gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:14559245 734134 Ncdn neurochondrin gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20220421 MGI PMID:20007903 734134 Ncdn neurochondrin gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:20007903 734134 Ncdn neurochondrin gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20007903 734134 Ncdn neurochondrin gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14559245 734134 Ncdn neurochondrin gene MP:0013454 lacrimal gland hypertrophy IAGP N RGD:5509061 20150205 MGI PMID:12904583 734137 Actn3 actinin alpha 3 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17828264 734137 Actn3 actinin alpha 3 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:17828264 734137 Actn3 actinin alpha 3 gene MP:0003060 increased aerobic running capacity IAGP N RGD:5509061 20141003 MGI PMID:17828264 734139 Sytl4 synaptotagmin-like 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16216924 734139 Sytl4 synaptotagmin-like 4 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210520 MGI 734139 Sytl4 synaptotagmin-like 4 gene MP:0001747 hypersecretion of adrenocorticotropin IAGP N RGD:5509061 20141003 MGI PMID:17761531 734139 Sytl4 synaptotagmin-like 4 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:16216924 734139 Sytl4 synaptotagmin-like 4 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:23223571 734139 Sytl4 synaptotagmin-like 4 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16216924 734139 Sytl4 synaptotagmin-like 4 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23223571 734139 Sytl4 synaptotagmin-like 4 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210520 MGI 734139 Sytl4 synaptotagmin-like 4 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16216924 734139 Sytl4 synaptotagmin-like 4 gene MP:0008327 abnormal corticotroph morphology IAGP N RGD:5509061 20141003 MGI PMID:17761531 734141 Ehd4 EH-domain containing 4 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20213691 734141 Ehd4 EH-domain containing 4 gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20213691 734141 Ehd4 EH-domain containing 4 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:20213691 734141 Ehd4 EH-domain containing 4 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:20213691 734141 Ehd4 EH-domain containing 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:20213691 734141 Ehd4 EH-domain containing 4 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220623 MGI PMID:20213691 734141 Ehd4 EH-domain containing 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20213691 734141 Ehd4 EH-domain containing 4 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:20213691 734141 Ehd4 EH-domain containing 4 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:20213691 734141 Ehd4 EH-domain containing 4 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:20213691 734141 Ehd4 EH-domain containing 4 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20213691 734141 Ehd4 EH-domain containing 4 gene MP:0006307 abnormal seminiferous tubule size IAGP N RGD:5509061 20141003 MGI PMID:20213691 734141 Ehd4 EH-domain containing 4 gene MP:0006308 enlarged seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:20213691 734141 Ehd4 EH-domain containing 4 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:20213691 734141 Ehd4 EH-domain containing 4 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0011369 increased renal glomerulus apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0011430 mesangiolysis IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0011455 absent glomerular endothelium fenestra IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0011512 mesangial cell interposition IAGP N RGD:5509061 20141003 MGI PMID:21408024 734141 Ehd4 EH-domain containing 4 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:20213691 734143 Rps24 ribosomal protein S24 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20191024 MGI PMID:26722357 734144 Runx3 runt related transcription factor 3 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0000161 scoliosis IAGP N RGD:5509061 20220616 MGI PMID:28829946 734144 Runx3 runt related transcription factor 3 gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20141003 MGI PMID:15937937 734144 Runx3 runt related transcription factor 3 gene MP:0000405 abnormal auchene hair morphology IAGP N RGD:5509061 20141003 MGI PMID:15937937 734144 Runx3 runt related transcription factor 3 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:15937937 734144 Runx3 runt related transcription factor 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11955451 734144 Runx3 runt related transcription factor 3 gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0001255 decreased body height IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 734144 Runx3 runt related transcription factor 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20151022 MGI PMID:19233693 734144 Runx3 runt related transcription factor 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20220616 MGI PMID:28829946 734144 Runx3 runt related transcription factor 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20201029 MGI PMID:32088381 734144 Runx3 runt related transcription factor 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20201029 MGI PMID:32088381 734144 Runx3 runt related transcription factor 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20220616 MGI PMID:28829946 734144 Runx3 runt related transcription factor 3 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0001513 limb grasping IAGP N RGD:5509061 20201029 MGI PMID:32088381 734144 Runx3 runt related transcription factor 3 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20201029 MGI PMID:32088381 734144 Runx3 runt related transcription factor 3 gene MP:0001525 impaired balance IAGP N RGD:5509061 20201029 MGI PMID:32088381 734144 Runx3 runt related transcription factor 3 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20151022 MGI PMID:19233693 734144 Runx3 runt related transcription factor 3 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20151022 MGI PMID:19233693 734144 Runx3 runt related transcription factor 3 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20151022 MGI PMID:19233693 734144 Runx3 runt related transcription factor 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:14765120 734144 Runx3 runt related transcription factor 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17646405 734144 Runx3 runt related transcription factor 3 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:16027362 734144 Runx3 runt related transcription factor 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20230615 MGI PMID:34803166 734144 Runx3 runt related transcription factor 3 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:14765120 734144 Runx3 runt related transcription factor 3 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14765120 734144 Runx3 runt related transcription factor 3 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16027362 734144 Runx3 runt related transcription factor 3 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18776905 734144 Runx3 runt related transcription factor 3 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:17646405 734144 Runx3 runt related transcription factor 3 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16027362 734144 Runx3 runt related transcription factor 3 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0003109 short femur IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0003994 abnormal dorsal spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0004142 abnormal muscle tone IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20201029 MGI PMID:32088381 734144 Runx3 runt related transcription factor 3 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20220616 MGI PMID:28829946 734144 Runx3 runt related transcription factor 3 gene MP:0004351 short humerus IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20151022 MGI PMID:19233693 734144 Runx3 runt related transcription factor 3 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16651517 734144 Runx3 runt related transcription factor 3 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17646405 734144 Runx3 runt related transcription factor 3 gene MP:0005211 increased stomach mucosa thickness IAGP N RGD:5509061 20141003 MGI PMID:11955451 734144 Runx3 runt related transcription factor 3 gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0005390 skeleton phenotype IAGP N RGD:5509061 20220616 MGI PMID:28829946 734144 Runx3 runt related transcription factor 3 gene MP:0005461 abnormal dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14765120 734144 Runx3 runt related transcription factor 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11955451 734144 Runx3 runt related transcription factor 3 gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0006282 abnormal spinal cord dorsal horn morphology IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14765120 734144 Runx3 runt related transcription factor 3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18258917 734144 Runx3 runt related transcription factor 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18258917 734144 Runx3 runt related transcription factor 3 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17646406 734144 Runx3 runt related transcription factor 3 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18258917 734144 Runx3 runt related transcription factor 3 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17646405 734144 Runx3 runt related transcription factor 3 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18776905 734144 Runx3 runt related transcription factor 3 gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14765120 734144 Runx3 runt related transcription factor 3 gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16651517 734144 Runx3 runt related transcription factor 3 gene MP:0008118 absent Langerhans cell IAGP N RGD:5509061 20141003 MGI PMID:14765120 734144 Runx3 runt related transcription factor 3 gene MP:0008118 absent Langerhans cell IAGP N RGD:5509061 20151022 MGI PMID:19233693 734144 Runx3 runt related transcription factor 3 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:14765120 734144 Runx3 runt related transcription factor 3 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:16027362 734144 Runx3 runt related transcription factor 3 gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0008273 abnormal intramembranous bone ossification IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0008467 absent proprioceptive neurons IAGP N RGD:5509061 20220616 MGI PMID:28829946 734144 Runx3 runt related transcription factor 3 gene MP:0008468 absent muscle spindles IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20141003 MGI PMID:18258917 734144 Runx3 runt related transcription factor 3 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20220616 MGI PMID:28829946 734144 Runx3 runt related transcription factor 3 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0010799 stomach mucosa hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11955451 734144 Runx3 runt related transcription factor 3 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11955451 734144 Runx3 runt related transcription factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12093746 734144 Runx3 runt related transcription factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15514019 734144 Runx3 runt related transcription factor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11955451 734144 Runx3 runt related transcription factor 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 734144 Runx3 runt related transcription factor 3 gene MP:0013639 decreased bone stiffness IAGP N RGD:5509061 20151022 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0014236 increased tumor-free survival time IAGP N RGD:5509061 20230615 MGI PMID:34803166 734144 Runx3 runt related transcription factor 3 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0021182 decreased femoral compact bone area IAGP N RGD:5509061 20220922 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0030315 small neurocranium IAGP N RGD:5509061 20171109 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0030439 decreased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:25605327 734144 Runx3 runt related transcription factor 3 gene MP:0031278 decreased osteosarcoma incidence IAGP N RGD:5509061 20230615 MGI PMID:34803166 734146 Cox5b cytochrome c oxidase subunit 5B gene MP:0000603 pale liver IEA N RGD:5509061 20210520 MGI 734146 Cox5b cytochrome c oxidase subunit 5B gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 734146 Cox5b cytochrome c oxidase subunit 5B gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 734146 Cox5b cytochrome c oxidase subunit 5B gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 734146 Cox5b cytochrome c oxidase subunit 5B gene MP:0004576 abnormal embryonic autopod plate morphology IEA N RGD:5509061 20170105 MGI 734146 Cox5b cytochrome c oxidase subunit 5B gene MP:0004848 abnormal liver size IEA N RGD:5509061 20170105 MGI 734146 Cox5b cytochrome c oxidase subunit 5B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 734146 Cox5b cytochrome c oxidase subunit 5B gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 734146 Cox5b cytochrome c oxidase subunit 5B gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 734148 Gabra4 gamma-aminobutyric acid type A receptor subunit alpha 4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 734148 Gabra4 gamma-aminobutyric acid type A receptor subunit alpha 4 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17005728 734148 Gabra4 gamma-aminobutyric acid type A receptor subunit alpha 4 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:17005728 734148 Gabra4 gamma-aminobutyric acid type A receptor subunit alpha 4 gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:17005728 734148 Gabra4 gamma-aminobutyric acid type A receptor subunit alpha 4 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17005728 734150 Selp selectin, platelet gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9329976 734150 Selp selectin, platelet gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10500197 734150 Selp selectin, platelet gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8551244 734150 Selp selectin, platelet gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9329976 734150 Selp selectin, platelet gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10228023 734150 Selp selectin, platelet gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10500197 734150 Selp selectin, platelet gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11050049 734150 Selp selectin, platelet gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:7535798 734150 Selp selectin, platelet gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:7579454 734150 Selp selectin, platelet gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:7688665 734150 Selp selectin, platelet gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9329976 734150 Selp selectin, platelet gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10500197 734150 Selp selectin, platelet gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:17456770 734150 Selp selectin, platelet gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:11050049 734150 Selp selectin, platelet gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9329976 734150 Selp selectin, platelet gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9329976 734150 Selp selectin, platelet gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:10228023 734150 Selp selectin, platelet gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:9329976 734150 Selp selectin, platelet gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9329976 734150 Selp selectin, platelet gene MP:0001411 spinning IAGP N RGD:5509061 20141003 MGI PMID:9329976 734150 Selp selectin, platelet gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20141003 MGI PMID:9329976 734150 Selp selectin, platelet gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:11050049 734150 Selp selectin, platelet gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:9329976 734150 Selp selectin, platelet gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:10670575 734150 Selp selectin, platelet gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:10228023 734150 Selp selectin, platelet gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:9329976 734150 Selp selectin, platelet gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11095738 734150 Selp selectin, platelet gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0002346 abnormal lymph node secondary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0002351 abnormal cervical lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9329976 734150 Selp selectin, platelet gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12096034 734150 Selp selectin, platelet gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:10228023 734150 Selp selectin, platelet gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:10453030 734150 Selp selectin, platelet gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:11095738 734150 Selp selectin, platelet gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:11050049 734150 Selp selectin, platelet gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:10453030 734150 Selp selectin, platelet gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:7535798 734150 Selp selectin, platelet gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0003627 abnormal leukocyte tethering or rolling IAGP N RGD:5509061 20141003 MGI PMID:8551244 734150 Selp selectin, platelet gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:11971023 734150 Selp selectin, platelet gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:10453030 734150 Selp selectin, platelet gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:7579454 734150 Selp selectin, platelet gene MP:0003946 renal necrosis IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10500197 734150 Selp selectin, platelet gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:10228023 734150 Selp selectin, platelet gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:9329976 734150 Selp selectin, platelet gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:8608210 734150 Selp selectin, platelet gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:17456770 734150 Selp selectin, platelet gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9817767 734150 Selp selectin, platelet gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0008623 increased circulating interleukin-3 level IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:10500197 734150 Selp selectin, platelet gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:7688665 734150 Selp selectin, platelet gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:9817767 734150 Selp selectin, platelet gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10228023 734150 Selp selectin, platelet gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:10500197 734150 Selp selectin, platelet gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11095738 734150 Selp selectin, platelet gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9817767 734150 Selp selectin, platelet gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0011483 renal glomerular synechia IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:17142777 734150 Selp selectin, platelet gene MP:0011514 skin hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8608210 734150 Selp selectin, platelet gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20240104 MGI PMID:11050049 734150 Selp selectin, platelet gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20240104 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0014351 abnormal spleen B cell follicle shape IAGP N RGD:5509061 20240104 MGI PMID:11050049 734150 Selp selectin, platelet gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:10500197 734150 Selp selectin, platelet gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:11468173 734150 Selp selectin, platelet gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:11971023 734150 Selp selectin, platelet gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:26631722 734150 Selp selectin, platelet gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:7579454 734150 Selp selectin, platelet gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:7688665 734150 Selp selectin, platelet gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:8551244 734150 Selp selectin, platelet gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:8598043 734150 Selp selectin, platelet gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:9817767 734152 Snap25 synaptosomal-associated protein 25 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:15470145 734152 Snap25 synaptosomal-associated protein 25 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19043548 734152 Snap25 synaptosomal-associated protein 25 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:11753414 734152 Snap25 synaptosomal-associated protein 25 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12451131 734152 Snap25 synaptosomal-associated protein 25 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:21949876 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:11753414 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001260 increased body weight IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15470145 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19043548 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19043548 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:19043548 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19043548 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21949876 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:21949876 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17283335 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19043548 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19043548 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:11753414 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:17283335 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20160616 MGI PMID:26300453 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19043548 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11753414 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:15470145 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11753414 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11753414 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:21949876 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:15470145 734152 Snap25 synaptosomal-associated protein 25 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11753414 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:19043548 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:10932191 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15470145 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:12451131 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11753414 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:11753414 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:15470145 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002711 decreased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:17283335 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:21949876 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:19043548 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:21949876 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002897 blotchy skin IAGP N RGD:5509061 20141003 MGI PMID:11753414 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11753414 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20141003 MGI PMID:11753414 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:15470145 734152 Snap25 synaptosomal-associated protein 25 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:19043548 734152 Snap25 synaptosomal-associated protein 25 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17283335 734152 Snap25 synaptosomal-associated protein 25 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:19043548 734152 Snap25 synaptosomal-associated protein 25 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17283335 734152 Snap25 synaptosomal-associated protein 25 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0004495 decreased synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:17283335 734152 Snap25 synaptosomal-associated protein 25 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:11753414 734152 Snap25 synaptosomal-associated protein 25 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17283335 734152 Snap25 synaptosomal-associated protein 25 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:21949876 734152 Snap25 synaptosomal-associated protein 25 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0006087 increased body mass index IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:19043548 734152 Snap25 synaptosomal-associated protein 25 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:19043548 734152 Snap25 synaptosomal-associated protein 25 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:17283335 734152 Snap25 synaptosomal-associated protein 25 gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20141003 MGI PMID:21949876 734152 Snap25 synaptosomal-associated protein 25 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15470145 734152 Snap25 synaptosomal-associated protein 25 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21949876 734152 Snap25 synaptosomal-associated protein 25 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11753414 734152 Snap25 synaptosomal-associated protein 25 gene MP:0011613 decreased circulating ghrelin level IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0011939 increased food intake IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20160519 MGI PMID:26195742 734152 Snap25 synaptosomal-associated protein 25 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:21949876 734154 Ptprn protein tyrosine phosphatase receptor type N gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20220120 MGI PMID:16269463 734154 Ptprn protein tyrosine phosphatase receptor type N gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20220120 MGI PMID:16269463 734154 Ptprn protein tyrosine phosphatase receptor type N gene MP:0001926 female infertility IAGP N RGD:5509061 20220120 MGI PMID:16269463 734154 Ptprn protein tyrosine phosphatase receptor type N gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20220120 MGI PMID:16269463 734154 Ptprn protein tyrosine phosphatase receptor type N gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20220120 MGI PMID:16269463 734154 Ptprn protein tyrosine phosphatase receptor type N gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220120 MGI PMID:16269463 734154 Ptprn protein tyrosine phosphatase receptor type N gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20220120 MGI PMID:16269463 734154 Ptprn protein tyrosine phosphatase receptor type N gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:14614561 734154 Ptprn protein tyrosine phosphatase receptor type N gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:14614561 734154 Ptprn protein tyrosine phosphatase receptor type N gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20220120 MGI PMID:16269463 734154 Ptprn protein tyrosine phosphatase receptor type N gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20220120 MGI PMID:16269463 734154 Ptprn protein tyrosine phosphatase receptor type N gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12031972 734156 Smad1 SMAD family member 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21420501 734156 Smad1 SMAD family member 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:21420501 734156 Smad1 SMAD family member 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21420501 734156 Smad1 SMAD family member 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20170323 MGI PMID:26076038 734156 Smad1 SMAD family member 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15899870 734156 Smad1 SMAD family member 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15899870 734156 Smad1 SMAD family member 1 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15899870 734156 Smad1 SMAD family member 1 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15899870 734156 Smad1 SMAD family member 1 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20220630 MGI PMID:35383354 734156 Smad1 SMAD family member 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:11784053 734156 Smad1 SMAD family member 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20220630 MGI PMID:35383354 734156 Smad1 SMAD family member 1 gene MP:0001749 suppressed circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:19819941 734156 Smad1 SMAD family member 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220630 MGI PMID:35383354 734156 Smad1 SMAD family member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17967875 734156 Smad1 SMAD family member 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20220630 MGI PMID:35383354 734156 Smad1 SMAD family member 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220630 MGI PMID:35383354 734156 Smad1 SMAD family member 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15899870 734156 Smad1 SMAD family member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19819941 734156 Smad1 SMAD family member 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:21420501 734156 Smad1 SMAD family member 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15899870 734156 Smad1 SMAD family member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21420501 734156 Smad1 SMAD family member 1 gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17967875 734156 Smad1 SMAD family member 1 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220630 MGI PMID:35383354 734156 Smad1 SMAD family member 1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0004140 abnormal gastric chief cell morphology IAGP N RGD:5509061 20150312 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0004558 delayed allantois development IAGP N RGD:5509061 20141003 MGI PMID:12351174 734156 Smad1 SMAD family member 1 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:21420501 734156 Smad1 SMAD family member 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:17967875 734156 Smad1 SMAD family member 1 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17967875 734156 Smad1 SMAD family member 1 gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:12351174 734156 Smad1 SMAD family member 1 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0006419 disorganized testis cords IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17967875 734156 Smad1 SMAD family member 1 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:12351174 734156 Smad1 SMAD family member 1 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0008393 absent primordial germ cells IAGP N RGD:5509061 20141003 MGI PMID:12351174 734156 Smad1 SMAD family member 1 gene MP:0008393 absent primordial germ cells IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0008393 absent primordial germ cells IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:17967875 734156 Smad1 SMAD family member 1 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20220630 MGI PMID:35383354 734156 Smad1 SMAD family member 1 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:21420501 734156 Smad1 SMAD family member 1 gene MP:0009649 delayed embryo implantation IAGP N RGD:5509061 20220630 MGI PMID:35383354 734156 Smad1 SMAD family member 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:11784053 734156 Smad1 SMAD family member 1 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20220630 MGI PMID:35383354 734156 Smad1 SMAD family member 1 gene MP:0009662 abnormal uterine receptivity IAGP N RGD:5509061 20220630 MGI PMID:35383354 734156 Smad1 SMAD family member 1 gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20220630 MGI PMID:35383354 734156 Smad1 SMAD family member 1 gene MP:0010642 absent third pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0010758 increased right ventricle systolic pressure IAGP N RGD:5509061 20170323 MGI PMID:26076038 734156 Smad1 SMAD family member 1 gene MP:0010779 abnormal stomach muscularis externa morphology IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:21420501 734156 Smad1 SMAD family member 1 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:21420501 734156 Smad1 SMAD family member 1 gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:21420501 734156 Smad1 SMAD family member 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11784053 734156 Smad1 SMAD family member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12351174 734156 Smad1 SMAD family member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:16765933 734156 Smad1 SMAD family member 1 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:21420501 734156 Smad1 SMAD family member 1 gene MP:0012134 absent umbilical cord IAGP N RGD:5509061 20141003 MGI PMID:11566864 734156 Smad1 SMAD family member 1 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:15198985 734156 Smad1 SMAD family member 1 gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19819941 734156 Smad1 SMAD family member 1 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20171221 MGI PMID:21420501 734156 Smad1 SMAD family member 1 gene MP:0030439 decreased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:21420501 734158 Rhoq ras homolog family member Q gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210826 MGI 734158 Rhoq ras homolog family member Q gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 734158 Rhoq ras homolog family member Q gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20230928 MGI PMID:33156548 734158 Rhoq ras homolog family member Q gene MP:0004220 abnormal peripheral nervous system regeneration IAGP N RGD:5509061 20230928 MGI PMID:33156548 734158 Rhoq ras homolog family member Q gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20230928 MGI PMID:33156548 734158 Rhoq ras homolog family member Q gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20230928 MGI PMID:33156548 734158 Rhoq ras homolog family member Q gene MP:0020850 abnormal microtubule cytoskeleton morphology IAGP N RGD:5509061 20230928 MGI PMID:33156548 734158 Rhoq ras homolog family member Q gene MP:0030012 impaired central nervous system regeneration IAGP N RGD:5509061 20230928 MGI PMID:33156548 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19816196 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20188654 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:6036114 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000745 tremors IAGP N RGD:5509061 20231214 MGI PMID:37862170 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20231214 MGI PMID:37862170 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:20188654 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000754 paresis IAGP N RGD:5509061 20231214 MGI PMID:37862170 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17549747 734160 Cntnap1 contactin associated protein-like 1 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:17549747 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20231214 MGI PMID:37862170 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19816196 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:6036114 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19816196 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20188654 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:6036114 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19816196 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:6036114 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20231214 MGI PMID:37862170 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:6036114 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20231214 MGI PMID:37862170 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19816196 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:6036114 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:6036114 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:6036114 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:19816196 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:6036114 734160 Cntnap1 contactin associated protein-like 1 gene MP:0001922 reduced male fertility IEA N RGD:5509061 20141003 MGI 734160 Cntnap1 contactin associated protein-like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:17549747 734160 Cntnap1 contactin associated protein-like 1 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:19816196 734160 Cntnap1 contactin associated protein-like 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:19816196 734160 Cntnap1 contactin associated protein-like 1 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20231214 MGI PMID:37862170 734160 Cntnap1 contactin associated protein-like 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:14676309 734160 Cntnap1 contactin associated protein-like 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19816196 734160 Cntnap1 contactin associated protein-like 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:20188654 734160 Cntnap1 contactin associated protein-like 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:5563943 734160 Cntnap1 contactin associated protein-like 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:19816196 734160 Cntnap1 contactin associated protein-like 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:20188654 734160 Cntnap1 contactin associated protein-like 1 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20231214 MGI PMID:37862170 734160 Cntnap1 contactin associated protein-like 1 gene MP:0009393 abnormal resting posture IAGP N RGD:5509061 20141003 MGI PMID:6036114 734160 Cntnap1 contactin associated protein-like 1 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0010732 abnormal node of Ranvier morphology IAGP N RGD:5509061 20141003 MGI PMID:19816196 734160 Cntnap1 contactin associated protein-like 1 gene MP:0010734 abnormal paranode morphology IAGP N RGD:5509061 20141003 MGI PMID:19816196 734160 Cntnap1 contactin associated protein-like 1 gene MP:0010734 abnormal paranode morphology IAGP N RGD:5509061 20231214 MGI PMID:37862170 734160 Cntnap1 contactin associated protein-like 1 gene MP:0010735 abnormal paranodal axoglial junction morphology IAGP N RGD:5509061 20141003 MGI PMID:19816196 734160 Cntnap1 contactin associated protein-like 1 gene MP:0010735 abnormal paranodal axoglial junction morphology IAGP N RGD:5509061 20231214 MGI PMID:37862170 734160 Cntnap1 contactin associated protein-like 1 gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20141003 MGI PMID:19816196 734160 Cntnap1 contactin associated protein-like 1 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19816196 734160 Cntnap1 contactin associated protein-like 1 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11395000 734160 Cntnap1 contactin associated protein-like 1 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20188654 734160 Cntnap1 contactin associated protein-like 1 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20231214 MGI PMID:37862170 734160 Cntnap1 contactin associated protein-like 1 gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:17549747 734160 Cntnap1 contactin associated protein-like 1 gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:16551741 734160 Cntnap1 contactin associated protein-like 1 gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:17549747 734161 Acvr1 activin A receptor, type 1 gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20171109 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20170921 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16140292 734161 Acvr1 activin A receptor, type 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:16140292 734161 Acvr1 activin A receptor, type 1 gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:16140292 734161 Acvr1 activin A receptor, type 1 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20200521 MGI PMID:32142668 734161 Acvr1 activin A receptor, type 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20200521 MGI PMID:32142668 734161 Acvr1 activin A receptor, type 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20200521 MGI PMID:32142668 734161 Acvr1 activin A receptor, type 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:10226013 734161 Acvr1 activin A receptor, type 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200521 MGI PMID:32142668 734161 Acvr1 activin A receptor, type 1 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:10226013 734161 Acvr1 activin A receptor, type 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:10479450 734161 Acvr1 activin A receptor, type 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:17117439 734161 Acvr1 activin A receptor, type 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10226013 734161 Acvr1 activin A receptor, type 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:10226013 734161 Acvr1 activin A receptor, type 1 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:17117439 734161 Acvr1 activin A receptor, type 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10226013 734161 Acvr1 activin A receptor, type 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10479450 734161 Acvr1 activin A receptor, type 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17117439 734161 Acvr1 activin A receptor, type 1 gene MP:0001710 absent amniotic folds IAGP N RGD:5509061 20141003 MGI PMID:10226013 734161 Acvr1 activin A receptor, type 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10479450 734161 Acvr1 activin A receptor, type 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17117439 734161 Acvr1 activin A receptor, type 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20170413 MGI PMID:26896819 734161 Acvr1 activin A receptor, type 1 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20170413 MGI PMID:26896819 734161 Acvr1 activin A receptor, type 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20170413 MGI PMID:26896819 734161 Acvr1 activin A receptor, type 1 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:10226013 734161 Acvr1 activin A receptor, type 1 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:10479450 734161 Acvr1 activin A receptor, type 1 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:17117439 734161 Acvr1 activin A receptor, type 1 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20170413 MGI PMID:26896819 734161 Acvr1 activin A receptor, type 1 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20170413 MGI PMID:26896819 734161 Acvr1 activin A receptor, type 1 gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:10226013 734161 Acvr1 activin A receptor, type 1 gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:10479450 734161 Acvr1 activin A receptor, type 1 gene MP:0003109 short femur IAGP N RGD:5509061 20170413 MGI PMID:26896819 734161 Acvr1 activin A receptor, type 1 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20170413 MGI PMID:26896819 734161 Acvr1 activin A receptor, type 1 gene MP:0003543 abnormal vascular endothelial cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16140292 734161 Acvr1 activin A receptor, type 1 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20200521 MGI PMID:32142668 734161 Acvr1 activin A receptor, type 1 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:10479450 734161 Acvr1 activin A receptor, type 1 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:17117439 734161 Acvr1 activin A receptor, type 1 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:10479450 734161 Acvr1 activin A receptor, type 1 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0004351 short humerus IAGP N RGD:5509061 20170413 MGI PMID:26896819 734161 Acvr1 activin A receptor, type 1 gene MP:0004355 short radius IAGP N RGD:5509061 20170413 MGI PMID:26896819 734161 Acvr1 activin A receptor, type 1 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0004635 short metatarsal bones IAGP N RGD:5509061 20141003 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20170413 MGI PMID:26896819 734161 Acvr1 activin A receptor, type 1 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:10226013 734161 Acvr1 activin A receptor, type 1 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20220519 MGI PMID:29396429 734161 Acvr1 activin A receptor, type 1 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20200521 MGI PMID:32142668 734161 Acvr1 activin A receptor, type 1 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 734161 Acvr1 activin A receptor, type 1 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0008069 abnormal joint mobility IAGP N RGD:5509061 20141003 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0008149 abnormal costovertebral joint morphology IAGP N RGD:5509061 20181011 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0008375 short malleus manubrium IAGP N RGD:5509061 20141003 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:16140292 734161 Acvr1 activin A receptor, type 1 gene MP:0009277 increased brain tumor incidence IAGP N RGD:5509061 20200521 MGI PMID:32142668 734161 Acvr1 activin A receptor, type 1 gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0009593 absent chorion IAGP N RGD:5509061 20141003 MGI PMID:10226013 734161 Acvr1 activin A receptor, type 1 gene MP:0009885 abnormal palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0010079 increased osteochondroma incidence IAGP N RGD:5509061 20141003 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0010160 increased oligodendrocyte number IAGP N RGD:5509061 20200521 MGI PMID:32142668 734161 Acvr1 activin A receptor, type 1 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20200521 MGI PMID:32142668 734161 Acvr1 activin A receptor, type 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16140292 734161 Acvr1 activin A receptor, type 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:16140292 734161 Acvr1 activin A receptor, type 1 gene MP:0010464 abnormal aortic arch and aortic arch branch attachment IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0010563 increased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0010587 conotruncal ridge hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0010592 abnormal atrioventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16140292 734161 Acvr1 activin A receptor, type 1 gene MP:0010663 abnormal brachiocephalic trunk morphology IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20200521 MGI PMID:32142668 734161 Acvr1 activin A receptor, type 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200521 MGI PMID:32142668 734161 Acvr1 activin A receptor, type 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10479450 734161 Acvr1 activin A receptor, type 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10226013 734161 Acvr1 activin A receptor, type 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210422 MGI 734161 Acvr1 activin A receptor, type 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16140292 734161 Acvr1 activin A receptor, type 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20200521 MGI PMID:32142668 734161 Acvr1 activin A receptor, type 1 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10226013 734161 Acvr1 activin A receptor, type 1 gene MP:0011190 thick embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:10226013 734161 Acvr1 activin A receptor, type 1 gene MP:0012749 decreased cardiac neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0012750 absent cardiac neural crest cells IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0012751 impaired cardiac neural crest cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:15226263 734161 Acvr1 activin A receptor, type 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20221103 MGI 734161 Acvr1 activin A receptor, type 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 734161 Acvr1 activin A receptor, type 1 gene MP:0014100 increased chondrocyte proliferation IAGP N RGD:5509061 20170413 MGI PMID:26896819 734161 Acvr1 activin A receptor, type 1 gene MP:0014167 ectopic bone IAGP N RGD:5509061 20160407 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20170309 MGI PMID:26333933 734161 Acvr1 activin A receptor, type 1 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20170413 MGI PMID:26896819 734161 Acvr1 activin A receptor, type 1 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20220519 MGI PMID:29396429 734161 Acvr1 activin A receptor, type 1 gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20220721 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0030111 absent temporomandibular joint IAGP N RGD:5509061 20171109 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0030120 absent retrotympanic process IAGP N RGD:5509061 20171005 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20171005 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0030170 absent mandibular symphysis IAGP N RGD:5509061 20171005 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0030283 small mandibular coronoid process IAGP N RGD:5509061 20171102 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0030311 abnormal mandibular fossa morphology IAGP N RGD:5509061 20171109 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0030379 abnormal frontal bone squamous part morphology IAGP N RGD:5509061 20171207 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0030416 absent temporal bone zygomatic process IAGP N RGD:5509061 20171207 MGI PMID:15037318 734161 Acvr1 activin A receptor, type 1 gene MP:0030793 short femur neck IAGP N RGD:5509061 20181011 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0030794 broad femur neck IAGP N RGD:5509061 20181011 MGI PMID:22508565 734161 Acvr1 activin A receptor, type 1 gene MP:0031128 cardiovascular shunt IAGP N RGD:5509061 20201015 MGI PMID:16140292 734161 Acvr1 activin A receptor, type 1 gene MP:0031550 abnormal atrioventricular valve development IAGP N RGD:5509061 20240104 MGI PMID:16140292 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:10359563 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:10468638 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:16267225 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10468638 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19012750 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19012750 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0001562 abnormal circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:12013525 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:10359563 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:12167591 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:9930871 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10359563 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10468638 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9930871 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0001926 female infertility IEA N RGD:5509061 20220519 MGI 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10359563 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10468638 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:9930871 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0002334 abnormal airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:10846038 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:10468638 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9930871 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:19012750 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:12167591 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:10468638 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:16886605 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:16977324 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:12423256 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:16267225 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15793296 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24089506 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:16977324 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:16886605 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0004504 decreased incidence of tumors by UV induction IAGP N RGD:5509061 20141003 MGI PMID:16977324 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:12423256 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17330822 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:14715958 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:16977324 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0005581 abnormal renin activity IAGP N RGD:5509061 20141003 MGI PMID:10359563 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:14715958 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:10830290 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:24089506 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:24089506 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:24089506 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0009373 abnormal cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:9751056 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0009374 absent cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:10468638 734162 Ptger2 prostaglandin E receptor 2 (subtype EP2) gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:11319164 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:21305688 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:11245568 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:11959834 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:22319578 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:11245568 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:15753214 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0000705 athymia IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:16781703 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15753214 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:16781703 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001096 abnormal glossopharyngeal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001100 abnormal vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220811 MGI PMID:35574006 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:11959834 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11959834 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21305688 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:22319578 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:22319578 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0001925 male infertility IAGP N RGD:5509061 20220811 MGI PMID:35574006 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:15753214 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16781703 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0002256 abnormal laryngeal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:22319578 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20040494 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:21305688 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20141003 MGI PMID:22319578 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004159 double aortic arch IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004161 cervical aortic arch IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:11245568 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:11959834 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:22319578 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:16611695 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:11959834 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004310 small otic vesicle IAGP N RGD:5509061 20141003 MGI PMID:22319578 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004311 otic vesicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004550 short trachea IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004551 decreased tracheal cartilage ring number IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004568 fusion of glossopharyngeal and vagus nerve IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:20040494 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20220811 MGI PMID:35574006 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20220811 MGI PMID:35574006 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11245568 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:11245568 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:22319578 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:22319578 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11959834 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11245568 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0009073 absent Wolffian ducts IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0009806 abnormal otic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:22319578 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0010464 abnormal aortic arch and aortic arch branch attachment IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0010488 abnormal left subclavian artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0010587 conotruncal ridge hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0010642 absent third pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:11959834 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0010642 absent third pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0010642 absent third pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:21305688 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0010643 absent fourth pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:21305688 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0010656 thick myocardium IAGP N RGD:5509061 20141003 MGI PMID:11245568 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0010939 abnormal mandibular prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:21305688 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16781703 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11959834 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21305688 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22319578 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0011232 abnormal vitamin A level IAGP N RGD:5509061 20141003 MGI PMID:16781703 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0011233 abnormal vitamin A metabolism IAGP N RGD:5509061 20141003 MGI PMID:22319578 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0011260 abnormal head mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:17067568 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:11959834 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:22319578 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0012493 absent pharyngeal arch arteries IAGP N RGD:5509061 20141003 MGI PMID:21305688 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0012707 incomplete caudal neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12563036 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0013165 absent forelimb buds IAGP N RGD:5509061 20141003 MGI PMID:22319578 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0013166 small forelimb buds IAGP N RGD:5509061 20141003 MGI PMID:22319578 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0013168 absent hindlimb buds IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0013283 failure of ventral body wall closure IAGP N RGD:5509061 20141003 MGI PMID:10192400 734164 Aldh1a2 aldehyde dehydrogenase family 1, subfamily A2 gene MP:0030249 small frontonasal prominence IAGP N RGD:5509061 20171019 MGI PMID:10192400 734167 Pex6 peroxisomal biogenesis factor 6 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 734167 Pex6 peroxisomal biogenesis factor 6 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210826 MGI 734167 Pex6 peroxisomal biogenesis factor 6 gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20210520 MGI 734167 Pex6 peroxisomal biogenesis factor 6 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20220811 MGI 734167 Pex6 peroxisomal biogenesis factor 6 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210826 MGI 734167 Pex6 peroxisomal biogenesis factor 6 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20210520 MGI 734167 Pex6 peroxisomal biogenesis factor 6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 734169 Mtnr1a melatonin receptor 1A gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20171012 MGI PMID:9247266 734169 Mtnr1a melatonin receptor 1A gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20200206 MGI PMID:19706469 734169 Mtnr1a melatonin receptor 1A gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200206 MGI PMID:19706469 734169 Mtnr1a melatonin receptor 1A gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20200206 MGI PMID:19706469 734169 Mtnr1a melatonin receptor 1A gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200206 MGI PMID:19706469 734169 Mtnr1a melatonin receptor 1A gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20200206 MGI PMID:19706469 734169 Mtnr1a melatonin receptor 1A gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200206 MGI PMID:19706469 734169 Mtnr1a melatonin receptor 1A gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200206 MGI PMID:19706469 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20160714 MGI PMID:23248154 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20150430 MGI 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20150430 MGI 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0001304 cataract IEA N RGD:5509061 20150430 MGI 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0001408 stereotypic behavior IEA N RGD:5509061 20170105 MGI 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0001512 trunk curl IEA N RGD:5509061 20170105 MGI 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:18292807 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0001523 impaired righting response IEA N RGD:5509061 20170105 MGI 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:18292807 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20160714 MGI PMID:23248154 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18292807 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18292807 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20160714 MGI PMID:23248154 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18292807 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:18292807 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:18292807 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20160714 MGI PMID:23248154 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20160714 MGI PMID:23248154 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0003929 decreased heart rate variability IAGP N RGD:5509061 20160714 MGI PMID:23248154 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20160714 MGI PMID:23248154 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:18292807 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20160714 MGI PMID:23248154 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:18292807 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:18292807 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20160714 MGI PMID:23248154 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20141003 MGI 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0010697 abnormal systemic arterial blood pressure regulation IAGP N RGD:5509061 20160714 MGI PMID:23248154 734175 Cyba cytochrome b-245, alpha polypeptide gene MP:0013799 abnormal intestinal goblet cell physiology IAGP N RGD:5509061 20150618 MGI PMID:24185898 734180 Opn1mw opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan) gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20181227 MGI PMID:28751656 734180 Opn1mw opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan) gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:14500905 734180 Opn1mw opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan) gene MP:0011831 abnormal visual contrast sensitivity IAGP N RGD:5509061 20151119 MGI PMID:22633808 734180 Opn1mw opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan) gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20181227 MGI PMID:28751656 734182 Arf6 ADP-ribosylation factor 6 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:16880525 734182 Arf6 ADP-ribosylation factor 6 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16880525 734182 Arf6 ADP-ribosylation factor 6 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16880525 734182 Arf6 ADP-ribosylation factor 6 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:16880525 734182 Arf6 ADP-ribosylation factor 6 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16880525 734182 Arf6 ADP-ribosylation factor 6 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16880525 734182 Arf6 ADP-ribosylation factor 6 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:16880525 734182 Arf6 ADP-ribosylation factor 6 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16880525 734182 Arf6 ADP-ribosylation factor 6 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16880525 734182 Arf6 ADP-ribosylation factor 6 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16880525 734182 Arf6 ADP-ribosylation factor 6 gene MP:0012246 abnormal hepatic cord morphology IAGP N RGD:5509061 20141003 MGI PMID:16880525 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:15601855 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:7596436 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:7596436 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0000730 increased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:20705734 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:20705734 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20705734 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22753193 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20705734 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:22753193 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:20705734 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:10357944 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:15601855 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15601855 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:7596436 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15601855 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:7596436 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:21248239 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15601855 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:20705734 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15601855 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:22753193 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20141003 MGI PMID:22753193 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20705734 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:21248239 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:7596436 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0003543 abnormal vascular endothelial cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15601855 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:15601855 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:18583712 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:9689083 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10357944 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:15698841 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15601855 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:7596436 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:22753193 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:17051153 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20705734 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:22753193 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:20705734 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15601855 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0009398 abnormal skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:20705734 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:20705734 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7596436 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15601855 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15601855 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20141003 MGI PMID:7596436 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0012200 increased endothelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22753193 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0012717 increased hemangioblast number IAGP N RGD:5509061 20141003 MGI PMID:10357944 734184 Flt1 FMS-like tyrosine kinase 1 gene MP:0020330 increased capillary density IAGP N RGD:5509061 20160714 MGI PMID:20705734 734186 Nrxn1 neurexin I gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20170105 MGI 734186 Nrxn1 neurexin I gene MP:0000745 tremors IEA N RGD:5509061 20160421 MGI 734186 Nrxn1 neurexin I gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:19822762 734186 Nrxn1 neurexin I gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:19822762 734186 Nrxn1 neurexin I gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:14983056 734186 Nrxn1 neurexin I gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12827191 734186 Nrxn1 neurexin I gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111215 MGI 734186 Nrxn1 neurexin I gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12827191 734186 Nrxn1 neurexin I gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:14983056 734186 Nrxn1 neurexin I gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:19822762 734186 Nrxn1 neurexin I gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12827191 734186 Nrxn1 neurexin I gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19822762 734186 Nrxn1 neurexin I gene MP:0002915 abnormal synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:12827191 734186 Nrxn1 neurexin I gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 734186 Nrxn1 neurexin I gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:11741895 734186 Nrxn1 neurexin I gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20190502 MGI 734186 Nrxn1 neurexin I gene MP:0003960 increased lean body mass IEA N RGD:5509061 20170105 MGI 734186 Nrxn1 neurexin I gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:12827191 734186 Nrxn1 neurexin I gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:12827191 734186 Nrxn1 neurexin I gene MP:0004494 abnormal synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:11741895 734186 Nrxn1 neurexin I gene MP:0004495 decreased synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:11741895 734186 Nrxn1 neurexin I gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19822762 734186 Nrxn1 neurexin I gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:12827191 734186 Nrxn1 neurexin I gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:12827191 734186 Nrxn1 neurexin I gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20170105 MGI 734186 Nrxn1 neurexin I gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 734186 Nrxn1 neurexin I gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 734186 Nrxn1 neurexin I gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 734186 Nrxn1 neurexin I gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20211021 MGI 734186 Nrxn1 neurexin I gene MP:0005574 decreased pulmonary respiratory rate IEA N RGD:5509061 20210128 MGI 734186 Nrxn1 neurexin I gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 734186 Nrxn1 neurexin I gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:19822762 734186 Nrxn1 neurexin I gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 734186 Nrxn1 neurexin I gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160421 MGI 734186 Nrxn1 neurexin I gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12827191 734186 Nrxn1 neurexin I gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12827191 734186 Nrxn1 neurexin I gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12827191 734186 Nrxn1 neurexin I gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:12827191 734186 Nrxn1 neurexin I gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 734190 Neu3 neuraminidase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22815940 734190 Neu3 neuraminidase 3 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22815940 734193 Lum lumican gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17911102 734193 Lum lumican gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:10644720 734193 Lum lumican gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:9606218 734193 Lum lumican gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9606218 734193 Lum lumican gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9606218 734193 Lum lumican gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9606218 734193 Lum lumican gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:11431438 734193 Lum lumican gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:9606218 734193 Lum lumican gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:10644720 734193 Lum lumican gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:11006226 734193 Lum lumican gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:12766039 734193 Lum lumican gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:17911102 734193 Lum lumican gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:9606218 734193 Lum lumican gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:10644720 734193 Lum lumican gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15051477 734193 Lum lumican gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17911102 734193 Lum lumican gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:10644720 734193 Lum lumican gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20170105 MGI 734193 Lum lumican gene MP:0002697 abnormal eye size IAGP N RGD:5509061 20141003 MGI PMID:12766039 734193 Lum lumican gene MP:0002698 abnormal sclera morphology IAGP N RGD:5509061 20141003 MGI PMID:12766039 734193 Lum lumican gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:10644720 734193 Lum lumican gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 734193 Lum lumican gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:9606218 734193 Lum lumican gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:11006226 734193 Lum lumican gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:12556382 734193 Lum lumican gene MP:0003094 abnormal cornea posterior stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:10644720 734193 Lum lumican gene MP:0003094 abnormal cornea posterior stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:11006226 734193 Lum lumican gene MP:0003095 abnormal cornea stroma development IAGP N RGD:5509061 20141003 MGI PMID:12556382 734193 Lum lumican gene MP:0003095 abnormal cornea stroma development IAGP N RGD:5509061 20141003 MGI PMID:9606218 734193 Lum lumican gene MP:0003096 increased corneal light-scattering IAGP N RGD:5509061 20141003 MGI PMID:11006226 734193 Lum lumican gene MP:0003096 increased corneal light-scattering IAGP N RGD:5509061 20141003 MGI PMID:12556382 734193 Lum lumican gene MP:0003098 decreased tendon stiffness IAGP N RGD:5509061 20141003 MGI PMID:12766039 734193 Lum lumican gene MP:0003099 retina detachment IAGP N RGD:5509061 20141003 MGI PMID:12766039 734193 Lum lumican gene MP:0003101 high myopia IAGP N RGD:5509061 20141003 MGI PMID:12766039 734193 Lum lumican gene MP:0003102 sclera thinning IAGP N RGD:5509061 20141003 MGI PMID:12766039 734193 Lum lumican gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:11006226 734193 Lum lumican gene MP:0005300 abnormal cornea stroma morphology IAGP N RGD:5509061 20141003 MGI PMID:9606218 734193 Lum lumican gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 734193 Lum lumican gene MP:0005353 abnormal patella morphology IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:9606218 734193 Lum lumican gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:11076963 734193 Lum lumican gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:17911102 734193 Lum lumican gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0009275 bruising IAGP N RGD:5509061 20141003 MGI PMID:12089156 734193 Lum lumican gene MP:0009275 bruising IAGP N RGD:5509061 20141003 MGI PMID:9606218 734193 Lum lumican gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 734193 Lum lumican gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:15051477 734193 Lum lumican gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:15051477 734193 Lum lumican gene MP:0020861 abnormal cornea wound healing IAGP N RGD:5509061 20181101 MGI PMID:10644720 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0008562 increased interferon-alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19668221 734197 Tank TRAF family member-associated Nf-kappa B activator gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:19668221 734199 Eml2 echinoderm microtubule associated protein like 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20170105 MGI 734199 Eml2 echinoderm microtubule associated protein like 2 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 734199 Eml2 echinoderm microtubule associated protein like 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20220811 MGI 734201 Hyou1 hypoxia up-regulated 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:19801575 734201 Hyou1 hypoxia up-regulated 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19801575 734201 Hyou1 hypoxia up-regulated 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19801575 734201 Hyou1 hypoxia up-regulated 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:19801575 734201 Hyou1 hypoxia up-regulated 1 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:15223375 734201 Hyou1 hypoxia up-regulated 1 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11714735 734201 Hyou1 hypoxia up-regulated 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11714735 734201 Hyou1 hypoxia up-regulated 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IEA N RGD:5509061 20141003 MGI 734201 Hyou1 hypoxia up-regulated 1 gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20141003 MGI PMID:17116640 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15922619 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10809963 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9892616 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0002855 abnormal cochlear ganglion morphology IAGP N RGD:5509061 20150122 MGI PMID:25194790 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15922619 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20210527 MGI PMID:24983315 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20150122 MGI PMID:25194790 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:19188446 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:17650334 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20150122 MGI PMID:25194790 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:12878730 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15922619 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9892616 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0006325 impaired hearing IAGP N RGD:5509061 20150122 MGI PMID:25194790 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:9892616 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:9892616 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:9892616 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12878730 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:19188446 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20150122 MGI PMID:25194790 734204 Mif macrophage migration inhibitory factor (glycosylation-inhibiting factor) gene MP:0031217 increased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20210527 MGI PMID:24983315 734208 Opn4 opsin 4 (melanopsin) gene MP:0001999 photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:16364902 734208 Opn4 opsin 4 (melanopsin) gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 734208 Opn4 opsin 4 (melanopsin) gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:21765429 734208 Opn4 opsin 4 (melanopsin) gene MP:0002638 abnormal pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:17325172 734208 Opn4 opsin 4 (melanopsin) gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20170525 MGI PMID:26392540 734208 Opn4 opsin 4 (melanopsin) gene MP:0006156 abnormal visual pursuit IAGP N RGD:5509061 20141003 MGI PMID:18432195 734208 Opn4 opsin 4 (melanopsin) gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:18432195 734208 Opn4 opsin 4 (melanopsin) gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:18545654 734208 Opn4 opsin 4 (melanopsin) gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:21765429 734208 Opn4 opsin 4 (melanopsin) gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20230713 MGI PMID:12808468 734208 Opn4 opsin 4 (melanopsin) gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:18545654 734208 Opn4 opsin 4 (melanopsin) gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:21765429 734208 Opn4 opsin 4 (melanopsin) gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12481141 734208 Opn4 opsin 4 (melanopsin) gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18432195 734208 Opn4 opsin 4 (melanopsin) gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22063212 734208 Opn4 opsin 4 (melanopsin) gene MP:0008847 abnormal suprachiasmatic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18432195 734208 Opn4 opsin 4 (melanopsin) gene MP:0008847 abnormal suprachiasmatic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18545654 734208 Opn4 opsin 4 (melanopsin) gene MP:0008847 abnormal suprachiasmatic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:21765429 734208 Opn4 opsin 4 (melanopsin) gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:22063212 734208 Opn4 opsin 4 (melanopsin) gene MP:0009639 abnormal olivary pretectal nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:21765429 734208 Opn4 opsin 4 (melanopsin) gene MP:0011831 abnormal visual contrast sensitivity IAGP N RGD:5509061 20151119 MGI PMID:22633808 734208 Opn4 opsin 4 (melanopsin) gene MP:0020468 abnormal circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:21765429 734208 Opn4 opsin 4 (melanopsin) gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:18432195 734208 Opn4 opsin 4 (melanopsin) gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:12481141 734208 Opn4 opsin 4 (melanopsin) gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:12808468 734208 Opn4 opsin 4 (melanopsin) gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:12481140 734208 Opn4 opsin 4 (melanopsin) gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:12481141 734208 Opn4 opsin 4 (melanopsin) gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:18432195 734208 Opn4 opsin 4 (melanopsin) gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:12808468 734208 Opn4 opsin 4 (melanopsin) gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:18432195 734208 Opn4 opsin 4 (melanopsin) gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:18545654 734208 Opn4 opsin 4 (melanopsin) gene MP:0020477 abnormal locomotor circadian rhythm IAGP N RGD:5509061 20171012 MGI PMID:18432195 734212 Fgf11 fibroblast growth factor 11 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20141003 MGI 734212 Fgf11 fibroblast growth factor 11 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20160804 MGI 734212 Fgf11 fibroblast growth factor 11 gene MP:0005316 abnormal response to tactile stimuli IEA N RGD:5509061 20141003 MGI 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9892694 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9892694 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9892694 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:20837540 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20837540 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20837540 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9892694 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20837540 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20837540 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:20837540 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:9892694 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9892694 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:20837540 734213 Serpinb2 serine (or cysteine) peptidase inhibitor, clade B, member 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220519 MGI 734215 Stk39 serine/threonine kinase 39 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20200604 MGI PMID:28442491 734215 Stk39 serine/threonine kinase 39 gene MP:0000231 hypertension IAGP N RGD:5509061 20200604 MGI PMID:28442491 734215 Stk39 serine/threonine kinase 39 gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:20813865 734215 Stk39 serine/threonine kinase 39 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:19307180 734215 Stk39 serine/threonine kinase 39 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20200604 MGI PMID:28442491 734215 Stk39 serine/threonine kinase 39 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20161103 MGI PMID:25994507 734215 Stk39 serine/threonine kinase 39 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20200604 MGI PMID:28442491 734215 Stk39 serine/threonine kinase 39 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:20813865 734215 Stk39 serine/threonine kinase 39 gene MP:0002871 albuminuria IEA N RGD:5509061 20111116 MGI 734215 Stk39 serine/threonine kinase 39 gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:20091762 734215 Stk39 serine/threonine kinase 39 gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:20813865 734215 Stk39 serine/threonine kinase 39 gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20161103 MGI PMID:25994507 734215 Stk39 serine/threonine kinase 39 gene MP:0003019 increased circulating chloride level IAGP N RGD:5509061 20200604 MGI PMID:28442491 734215 Stk39 serine/threonine kinase 39 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20161103 MGI PMID:25994507 734215 Stk39 serine/threonine kinase 39 gene MP:0003028 alkalosis IAGP N RGD:5509061 20200604 MGI PMID:28442491 734215 Stk39 serine/threonine kinase 39 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20200604 MGI PMID:28442491 734215 Stk39 serine/threonine kinase 39 gene MP:0003916 decreased heart left ventricle weight IAGP N RGD:5509061 20161103 MGI PMID:25994507 734215 Stk39 serine/threonine kinase 39 gene MP:0004119 hypokalemia IAGP N RGD:5509061 20141003 MGI PMID:20091762 734215 Stk39 serine/threonine kinase 39 gene MP:0004119 hypokalemia IAGP N RGD:5509061 20200604 MGI PMID:28442491 734215 Stk39 serine/threonine kinase 39 gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20200604 MGI PMID:28442491 734215 Stk39 serine/threonine kinase 39 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:19307180 734215 Stk39 serine/threonine kinase 39 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20091762 734215 Stk39 serine/threonine kinase 39 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20161103 MGI PMID:25994507 734215 Stk39 serine/threonine kinase 39 gene MP:0004879 decreased systemic vascular resistance IAGP N RGD:5509061 20161103 MGI PMID:25994507 734215 Stk39 serine/threonine kinase 39 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20161103 MGI PMID:25994507 734215 Stk39 serine/threonine kinase 39 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20200604 MGI PMID:28442491 734215 Stk39 serine/threonine kinase 39 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20200604 MGI PMID:28442491 734215 Stk39 serine/threonine kinase 39 gene MP:0005583 decreased renin activity IAGP N RGD:5509061 20200604 MGI PMID:28442491 734215 Stk39 serine/threonine kinase 39 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20200604 MGI PMID:28442491 734215 Stk39 serine/threonine kinase 39 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:20091762 734215 Stk39 serine/threonine kinase 39 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:20813865 734215 Stk39 serine/threonine kinase 39 gene MP:0005628 decreased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:20813865 734215 Stk39 serine/threonine kinase 39 gene MP:0005628 decreased circulating potassium level IAGP N RGD:5509061 20161103 MGI PMID:25994507 734215 Stk39 serine/threonine kinase 39 gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20161103 MGI PMID:25994507 734215 Stk39 serine/threonine kinase 39 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20161103 MGI PMID:25994507 734215 Stk39 serine/threonine kinase 39 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:20091762 734215 Stk39 serine/threonine kinase 39 gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20161103 MGI PMID:25994507 734215 Stk39 serine/threonine kinase 39 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:20813865 734215 Stk39 serine/threonine kinase 39 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20813865 734215 Stk39 serine/threonine kinase 39 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:20091762 734215 Stk39 serine/threonine kinase 39 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:20813865 734215 Stk39 serine/threonine kinase 39 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20161103 MGI PMID:25994507 734215 Stk39 serine/threonine kinase 39 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20200604 MGI PMID:28442491 734215 Stk39 serine/threonine kinase 39 gene MP:0011435 increased urine magnesium level IAGP N RGD:5509061 20141003 MGI PMID:20813865 734215 Stk39 serine/threonine kinase 39 gene MP:0011460 decreased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:20813865 734215 Stk39 serine/threonine kinase 39 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20161103 MGI PMID:25994507 734215 Stk39 serine/threonine kinase 39 gene MP:0012339 hyperkalemia IAGP N RGD:5509061 20200604 MGI PMID:28442491 734215 Stk39 serine/threonine kinase 39 gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20200604 MGI PMID:28442491 734217 Ank3 ankyrin 3, epithelial gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9832557 734217 Ank3 ankyrin 3, epithelial gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9832557 734217 Ank3 ankyrin 3, epithelial gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:9832557 734217 Ank3 ankyrin 3, epithelial gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:9832557 734217 Ank3 ankyrin 3, epithelial gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:9832557 734217 Ank3 ankyrin 3, epithelial gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:9832557 734217 Ank3 ankyrin 3, epithelial gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9832557 734217 Ank3 ankyrin 3, epithelial gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9832557 734217 Ank3 ankyrin 3, epithelial gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9832557 734217 Ank3 ankyrin 3, epithelial gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20170413 MGI PMID:25552556 734217 Ank3 ankyrin 3, epithelial gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20170413 MGI PMID:25552556 734217 Ank3 ankyrin 3, epithelial gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9832557 734217 Ank3 ankyrin 3, epithelial gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20170413 MGI PMID:25552556 734217 Ank3 ankyrin 3, epithelial gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:9832557 734217 Ank3 ankyrin 3, epithelial gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20170413 MGI PMID:25552556 734217 Ank3 ankyrin 3, epithelial gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20170413 MGI PMID:25552556 734217 Ank3 ankyrin 3, epithelial gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20170413 MGI PMID:25552556 734217 Ank3 ankyrin 3, epithelial gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20170413 MGI PMID:25552556 734217 Ank3 ankyrin 3, epithelial gene MP:0010053 decreased grip strength IEA N RGD:5509061 20230601 MGI 734217 Ank3 ankyrin 3, epithelial gene MP:0010732 abnormal node of Ranvier morphology IAGP N RGD:5509061 20170413 MGI PMID:25552556 734217 Ank3 ankyrin 3, epithelial gene MP:0010733 abnormal axon initial segment morphology IAGP N RGD:5509061 20170413 MGI PMID:25552556 734217 Ank3 ankyrin 3, epithelial gene MP:0010735 abnormal paranodal axoglial junction morphology IAGP N RGD:5509061 20170413 MGI PMID:25552556 734217 Ank3 ankyrin 3, epithelial gene MP:0010943 abnormal bronchus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23530049 734217 Ank3 ankyrin 3, epithelial gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23530049 734217 Ank3 ankyrin 3, epithelial gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 734217 Ank3 ankyrin 3, epithelial gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23530049 734217 Ank3 ankyrin 3, epithelial gene MP:0011843 abnormal kidney collecting duct epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23530049 734217 Ank3 ankyrin 3, epithelial gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:25552556 734221 Nucb2 nucleobindin 2 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20220721 MGI PMID:30067966 734221 Nucb2 nucleobindin 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20220721 MGI PMID:30067966 734221 Nucb2 nucleobindin 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20111116 MGI 734221 Nucb2 nucleobindin 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20220721 MGI PMID:30067966 734221 Nucb2 nucleobindin 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20220721 MGI PMID:30067966 734221 Nucb2 nucleobindin 2 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20111116 MGI 734221 Nucb2 nucleobindin 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20220721 MGI PMID:30067966 734221 Nucb2 nucleobindin 2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20220721 MGI PMID:30067966 734221 Nucb2 nucleobindin 2 gene MP:0020102 increased hepatic glucose production IAGP N RGD:5509061 20220721 MGI PMID:30067966 734225 Hoxa5 homeobox A5 gene MP:0000054 delayed ear emergence IAGP N RGD:5509061 20141003 MGI PMID:12815622 734225 Hoxa5 homeobox A5 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7901120 734225 Hoxa5 homeobox A5 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:7901120 734225 Hoxa5 homeobox A5 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:17626057 734225 Hoxa5 homeobox A5 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:7901120 734225 Hoxa5 homeobox A5 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:24307483 734225 Hoxa5 homeobox A5 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:24307483 734225 Hoxa5 homeobox A5 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:7901120 734225 Hoxa5 homeobox A5 gene MP:0000501 abnormal digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:10564089 734225 Hoxa5 homeobox A5 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:24307483 734225 Hoxa5 homeobox A5 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:17417799 734225 Hoxa5 homeobox A5 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:12815622 734225 Hoxa5 homeobox A5 gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12815622 734225 Hoxa5 homeobox A5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20150806 MGI PMID:22315454 734225 Hoxa5 homeobox A5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:24307483 734225 Hoxa5 homeobox A5 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:17417799 734225 Hoxa5 homeobox A5 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20150806 MGI PMID:22315454 734225 Hoxa5 homeobox A5 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 734225 Hoxa5 homeobox A5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17417799 734225 Hoxa5 homeobox A5 gene MP:0002249 abnormal larynx morphology IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0002258 abnormal cricoid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0002267 abnormal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:17417799 734225 Hoxa5 homeobox A5 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:24307483 734225 Hoxa5 homeobox A5 gene MP:0002281 abnormal respiratory mucosa goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:24307483 734225 Hoxa5 homeobox A5 gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:17626057 734225 Hoxa5 homeobox A5 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 734225 Hoxa5 homeobox A5 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17417799 734225 Hoxa5 homeobox A5 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:24307483 734225 Hoxa5 homeobox A5 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:17417799 734225 Hoxa5 homeobox A5 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:17626057 734225 Hoxa5 homeobox A5 gene MP:0003378 early sexual maturation IAGP N RGD:5509061 20150806 MGI PMID:22315454 734225 Hoxa5 homeobox A5 gene MP:0003421 abnormal thyroid gland development IAGP N RGD:5509061 20141003 MGI PMID:12815622 734225 Hoxa5 homeobox A5 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 734225 Hoxa5 homeobox A5 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:17626057 734225 Hoxa5 homeobox A5 gene MP:0004551 decreased tracheal cartilage ring number IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 734225 Hoxa5 homeobox A5 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7901120 734225 Hoxa5 homeobox A5 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7901120 734225 Hoxa5 homeobox A5 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17626057 734225 Hoxa5 homeobox A5 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:17626057 734225 Hoxa5 homeobox A5 gene MP:0004625 abnormal rib joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 734225 Hoxa5 homeobox A5 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0004880 lung cyst IAGP N RGD:5509061 20200430 MGI PMID:21309069 734225 Hoxa5 homeobox A5 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12815622 734225 Hoxa5 homeobox A5 gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20150806 MGI PMID:22315454 734225 Hoxa5 homeobox A5 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17626057 734225 Hoxa5 homeobox A5 gene MP:0005629 abnormal lung weight IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:7901120 734225 Hoxa5 homeobox A5 gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20150806 MGI PMID:22315454 734225 Hoxa5 homeobox A5 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20150806 MGI PMID:22315454 734225 Hoxa5 homeobox A5 gene MP:0009018 short estrus IAGP N RGD:5509061 20150806 MGI PMID:22315454 734225 Hoxa5 homeobox A5 gene MP:0009020 prolonged metestrus IAGP N RGD:5509061 20150806 MGI PMID:22315454 734225 Hoxa5 homeobox A5 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0009438 cricoid and tracheal cartilage fusion IAGP N RGD:5509061 20141003 MGI PMID:17417799 734225 Hoxa5 homeobox A5 gene MP:0009438 cricoid and tracheal cartilage fusion IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:7901120 734225 Hoxa5 homeobox A5 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:17626057 734225 Hoxa5 homeobox A5 gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0010861 increased respiratory mucosa goblet cell number IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0010861 increased respiratory mucosa goblet cell number IAGP N RGD:5509061 20141003 MGI PMID:17417799 734225 Hoxa5 homeobox A5 gene MP:0010883 trachea stenosis IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0010897 abnormal bronchiole epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0010901 abnormal pulmonary alveolar parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:17003488 734225 Hoxa5 homeobox A5 gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20200430 MGI PMID:21309069 734225 Hoxa5 homeobox A5 gene MP:0010911 abnormal pulmonary acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0010943 abnormal bronchus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:12815622 734225 Hoxa5 homeobox A5 gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20150212 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0011034 impaired branching involved in respiratory bronchiole morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7901120 734225 Hoxa5 homeobox A5 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17417799 734225 Hoxa5 homeobox A5 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9441679 734225 Hoxa5 homeobox A5 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24307483 734225 Hoxa5 homeobox A5 gene MP:0012284 increased sternebra number IAGP N RGD:5509061 20141003 MGI PMID:7901120 734225 Hoxa5 homeobox A5 gene MP:0012668 absent sternal manubrium IAGP N RGD:5509061 20141003 MGI PMID:17626057 734225 Hoxa5 homeobox A5 gene MP:0013497 trachea occlusion IAGP N RGD:5509061 20150212 MGI PMID:9441679 734226 Cpb1 carboxypeptidase B1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 734226 Cpb1 carboxypeptidase B1 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 734230 Tdrd7 tudor domain containing 7 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21670278 734230 Tdrd7 tudor domain containing 7 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21436445 734230 Tdrd7 tudor domain containing 7 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21670278 734230 Tdrd7 tudor domain containing 7 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:21436445 734230 Tdrd7 tudor domain containing 7 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:21436445 734230 Tdrd7 tudor domain containing 7 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:21436445 734230 Tdrd7 tudor domain containing 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21436445 734230 Tdrd7 tudor domain containing 7 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21670278 734230 Tdrd7 tudor domain containing 7 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21436445 734230 Tdrd7 tudor domain containing 7 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:21670278 734230 Tdrd7 tudor domain containing 7 gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20141003 MGI PMID:21436445 734230 Tdrd7 tudor domain containing 7 gene MP:0005515 uveitis IAGP N RGD:5509061 20141003 MGI PMID:21436445 734230 Tdrd7 tudor domain containing 7 gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20141003 MGI PMID:21670278 734230 Tdrd7 tudor domain containing 7 gene MP:0006222 optic neuropathy IAGP N RGD:5509061 20141003 MGI PMID:21436445 734230 Tdrd7 tudor domain containing 7 gene MP:0008841 ruptured lens capsule IAGP N RGD:5509061 20141003 MGI PMID:21436445 734230 Tdrd7 tudor domain containing 7 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:21670278 734230 Tdrd7 tudor domain containing 7 gene MP:0031213 increased eye anterior chamber depth IAGP N RGD:5509061 20201231 MGI PMID:21436445 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:24225147 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:24225147 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:24225147 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:24225147 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:20051516 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:24225147 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:20051516 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:24225147 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:24225147 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0003285 gastric hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21084694 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:21084694 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:24225147 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20150122 MGI PMID:24727472 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20231207 MGI 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0006335 abnormal hearing electrophysiology IAGP N RGD:5509061 20150122 MGI PMID:24727472 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0008003 achlorhydria IAGP N RGD:5509061 20141003 MGI PMID:21084694 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20141003 MGI PMID:21084694 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20051516 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:24225147 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:20051516 734232 Kcne3 potassium voltage-gated channel, Isk-related subfamily, gene 3 gene MP:0010505 abnormal T wave IAGP N RGD:5509061 20141003 MGI PMID:24225147 734234 Fdxr ferredoxin reductase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20171207 MGI PMID:29040572 734234 Fdxr ferredoxin reductase gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0002083 premature death IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20171207 MGI PMID:29040572 734234 Fdxr ferredoxin reductase gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20171207 MGI PMID:29040572 734234 Fdxr ferredoxin reductase gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20171207 MGI PMID:29040572 734234 Fdxr ferredoxin reductase gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0009439 increased myeloid sarcoma incidence IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0010736 abnormal extraembryonic ectoderm morphology IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 734234 Fdxr ferredoxin reductase gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20171207 MGI PMID:29040572 734234 Fdxr ferredoxin reductase gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0012555 decreased cell death IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0012602 increased alpha-fetoprotein level IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0014136 abnormal extraembryonic endoderm morphology IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0014141 abnormal mesoderm morphology IAGP N RGD:5509061 20210617 MGI PMID:28747430 734234 Fdxr ferredoxin reductase gene MP:0031301 chronic liver inflammation IAGP N RGD:5509061 20211028 MGI PMID:28747430 734236 Ciita class II transactivator gene MP:0000066 osteoporosis IAGP N RGD:5509061 20160825 MGI PMID:24038328 734236 Ciita class II transactivator gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20160825 MGI PMID:24038328 734236 Ciita class II transactivator gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10201997 734236 Ciita class II transactivator gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17072917 734236 Ciita class II transactivator gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:9164958 734236 Ciita class II transactivator gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:10452977 734236 Ciita class II transactivator gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:10201997 734236 Ciita class II transactivator gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:10201997 734236 Ciita class II transactivator gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15446308 734236 Ciita class II transactivator gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10201997 734236 Ciita class II transactivator gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9164958 734236 Ciita class II transactivator gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11532347 734236 Ciita class II transactivator gene MP:0002352 abnormal popliteal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:9164958 734236 Ciita class II transactivator gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15661876 734236 Ciita class II transactivator gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8624807 734236 Ciita class II transactivator gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15661876 734236 Ciita class II transactivator gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15322541 734236 Ciita class II transactivator gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10452977 734236 Ciita class II transactivator gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:9164958 734236 Ciita class II transactivator gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20160825 MGI PMID:24038328 734236 Ciita class II transactivator gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:10452977 734236 Ciita class II transactivator gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15661876 734236 Ciita class II transactivator gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:15446308 734236 Ciita class II transactivator gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:11937578 734236 Ciita class II transactivator gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:15446308 734236 Ciita class II transactivator gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20160825 MGI PMID:24038328 734236 Ciita class II transactivator gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20160825 MGI PMID:24038328 734236 Ciita class II transactivator gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9164958 734236 Ciita class II transactivator gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9164958 734236 Ciita class II transactivator gene MP:0005040 abnormal MHC II cell surface expression on macrophages IAGP N RGD:5509061 20141003 MGI PMID:8624807 734236 Ciita class II transactivator gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:10201997 734236 Ciita class II transactivator gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:15661876 734236 Ciita class II transactivator gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:8624807 734236 Ciita class II transactivator gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:9491996 734236 Ciita class II transactivator gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:9885917 734236 Ciita class II transactivator gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10452977 734236 Ciita class II transactivator gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8624807 734236 Ciita class II transactivator gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8624807 734236 Ciita class II transactivator gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:11937578 734236 Ciita class II transactivator gene MP:0005580 periinsulitis IAGP N RGD:5509061 20141003 MGI PMID:10201997 734236 Ciita class II transactivator gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9164958 734236 Ciita class II transactivator gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10201997 734236 Ciita class II transactivator gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10452977 734236 Ciita class II transactivator gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15322541 734236 Ciita class II transactivator gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8624807 734236 Ciita class II transactivator gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9885917 734236 Ciita class II transactivator gene MP:0008076 abnormal CD4-positive T cell differentiation IEA N RGD:5509061 20150702 MGI 734236 Ciita class II transactivator gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10201997 734236 Ciita class II transactivator gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10452977 734236 Ciita class II transactivator gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9164958 734236 Ciita class II transactivator gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IEA N RGD:5509061 20150702 MGI 734236 Ciita class II transactivator gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:15446308 734236 Ciita class II transactivator gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:9885917 734236 Ciita class II transactivator gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20160825 MGI PMID:24038328 734236 Ciita class II transactivator gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20160825 MGI PMID:24038328 734236 Ciita class II transactivator gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20160825 MGI PMID:24038328 734236 Ciita class II transactivator gene MP:0020154 impaired humoral immune response IEA N RGD:5509061 20150702 MGI 734236 Ciita class II transactivator gene MP:0031074 increased circulating type I collagen C-terminal telopeptide level IAGP N RGD:5509061 20200618 MGI PMID:24038328 734240 Prom2 prominin 2 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 734240 Prom2 prominin 2 gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20170406 MGI 734240 Prom2 prominin 2 gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20170105 MGI 734240 Prom2 prominin 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 734240 Prom2 prominin 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 734240 Prom2 prominin 2 gene MP:0001577 anemia IEA N RGD:5509061 20170406 MGI 734240 Prom2 prominin 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20170406 MGI 734240 Prom2 prominin 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 734240 Prom2 prominin 2 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20211021 MGI 734240 Prom2 prominin 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 734240 Prom2 prominin 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20170406 MGI 734240 Prom2 prominin 2 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210520 MGI 734240 Prom2 prominin 2 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20211021 MGI 734240 Prom2 prominin 2 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210520 MGI 734240 Prom2 prominin 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160421 MGI 734240 Prom2 prominin 2 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20211021 MGI 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20151231 MGI PMID:24528488 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20151231 MGI PMID:24528488 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20151231 MGI PMID:24528488 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20151231 MGI PMID:24528488 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20151231 MGI PMID:24528488 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20151231 MGI PMID:24528488 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20151231 MGI PMID:24528488 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20151231 MGI PMID:24528488 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0008431 abnormal short-term spatial reference memory IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20151231 MGI PMID:24528488 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0013189 abnormal exploration in a new environment IAGP N RGD:5509061 20160602 MGI PMID:27042284 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0030981 abnormal dentate gyrus subgranular zone morphology IAGP N RGD:5509061 20191017 MGI PMID:24528488 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:24528488 734244 Brinp1 bone morphogenic protein/retinoic acid inducible neural specific 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:27042284 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22791713 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20220519 MGI 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20180510 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001147 small testis IAGP N RGD:5509061 20180510 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001147 small testis IAGP N RGD:5509061 20220203 MGI PMID:24371141 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20180510 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20220203 MGI PMID:24371141 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220203 MGI PMID:24371141 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001200 thick skin IEA N RGD:5509061 20220519 MGI 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001258 decreased body length IEA N RGD:5509061 20200514 MGI 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22791713 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220203 MGI PMID:24371141 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22791713 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20180510 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220203 MGI PMID:24371141 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001925 male infertility IAGP N RGD:5509061 20180510 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001925 male infertility IAGP N RGD:5509061 20220203 MGI PMID:24371141 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220203 MGI PMID:24371141 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20180510 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220203 MGI PMID:24371141 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210826 MGI 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20180510 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20220203 MGI PMID:24371141 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20180510 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220203 MGI PMID:24371141 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20220203 MGI PMID:24371141 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20200514 MGI 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22791713 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22791713 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20180510 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220203 MGI PMID:24371141 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220203 MGI PMID:24371141 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220203 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:22791713 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22791713 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20180510 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20180510 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180510 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:22791713 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:22791713 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:22791713 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20231207 MGI 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180510 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20180510 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20141003 MGI PMID:22791713 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220203 MGI PMID:24371141 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:22791713 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0012109 decreased trophoblast glycogen cell number IAGP N RGD:5509061 20141003 MGI PMID:22791713 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20180510 MGI PMID:27666520 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220203 MGI PMID:24371141 734246 Ptp4a2 protein tyrosine phosphatase 4a2 gene MP:0020362 abnormal male germ cell physiology IAGP N RGD:5509061 20220203 MGI PMID:24371141 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000003 abnormal adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10359811 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17266397 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11455125 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210128 MGI 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9647244 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22011580 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20210128 MGI 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20210128 MGI 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10702415 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:22972987 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23871670 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:23871670 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22011580 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:9177215 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:10702415 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:9736029 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10898787 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20210826 MGI PMID:33210082 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:24211183 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:18772111 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18772111 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:24211183 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22011580 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10702415 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15334086 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:18408078 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:20713516 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12163535 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:18329246 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22011580 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:10702415 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9688988 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:8395024 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:9551933 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:18641654 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15334086 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:10702415 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:10702415 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15289505 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:20713516 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:23871670 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:10702415 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:11238652 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12370348 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:9647244 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:11238652 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9551933 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:18408078 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:14661063 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11120777 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16988041 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10195897 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18772111 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15334086 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18408078 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20713516 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22011580 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23871670 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002083 premature death IAGP N RGD:5509061 20210826 MGI PMID:33210082 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11292619 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20141003 MGI PMID:17435079 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002334 abnormal airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:12370348 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002334 abnormal airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:17435079 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002343 abnormal lymph node cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9647244 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:9177215 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002345 abnormal lymph node primary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9647244 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002346 abnormal lymph node secondary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9647244 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:10702415 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:18641654 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9177215 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15289505 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17353199 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8387893 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9820556 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10595943 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8395024 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9551933 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002450 abnormal lymph organ development IAGP N RGD:5509061 20141003 MGI PMID:10843380 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20457915 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:10377141 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20181227 MGI 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23871670 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002658 abnormal liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:23871670 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10359811 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:22011580 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:10606630 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002816 colitis IAGP N RGD:5509061 20210826 MGI PMID:33210082 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:22011580 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:19285115 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23871670 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:9820556 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:15289505 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:18250193 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20210826 MGI PMID:33210082 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20141003 MGI PMID:11455125 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15289505 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:10779546 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:10898787 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11292619 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:18250193 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:24089213 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:17724122 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20713516 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23871670 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:12133972 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:12205053 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:16988041 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:9736029 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:23676465 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12205053 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0004254 cerebral amyloid angiopathy IAGP N RGD:5509061 20141003 MGI PMID:17724122 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0004574 broad limb buds IAGP N RGD:5509061 20141003 MGI PMID:10898787 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:15289505 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:10064079 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16237080 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:22011580 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10946317 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10946317 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:8673925 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0004822 decreased susceptibility to experimental autoimmune uveoretinitis IAGP N RGD:5509061 20141003 MGI PMID:10509653 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:22972987 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:24211183 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:10595943 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:18329246 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9647244 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9647244 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:10329607 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:14617760 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:15334086 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005190 osteomyelitis IAGP N RGD:5509061 20141003 MGI PMID:10595943 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:10843380 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:10359811 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20240523 MGI 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23871670 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:23871670 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:9647244 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:20713516 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005543 decreased cornea thickness IAGP N RGD:5509061 20141003 MGI PMID:20713516 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:10946317 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:15366373 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20713516 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:9846974 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:8673925 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008044 increased NK cell number IEA N RGD:5509061 20230601 MGI 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:9177215 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:9647244 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008196 abnormal follicular dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20457915 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008201 absent follicular dendritic cells IAGP N RGD:5509061 20141003 MGI PMID:9177215 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:8673925 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:9647244 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:10702415 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:10064079 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008523 absent lymph node germinal center IAGP N RGD:5509061 20141003 MGI PMID:9647244 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20530205 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:20530205 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:10204494 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:18641654 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:20457915 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:9551933 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20190117 MGI PMID:26195802 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:10204494 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18719121 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:20457915 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:23676465 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:20457915 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20457915 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:10509653 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20457915 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:8395024 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:11238652 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:11238652 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20457915 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:20457915 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:9551933 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:20457915 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:14557383 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9846974 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:17724122 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:21658601 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:23676465 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15289505 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20457915 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23676465 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20457915 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23676465 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9688988 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:14557383 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18641654 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23676465 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:8387893 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20161201 MGI PMID:16988041 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0010042 abnormal oval cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11120777 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16282134 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:23676465 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0010537 tumor regression IAGP N RGD:5509061 20141003 MGI PMID:23676465 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20230601 MGI 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18329246 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:20457915 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10702415 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24211183 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22972987 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10898787 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18408078 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22011580 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23871670 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210826 MGI PMID:33210082 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:12205053 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:9688988 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:23871670 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0011982 decreased microglial cell number IAGP N RGD:5509061 20161201 MGI PMID:16988041 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20181227 MGI 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:16079187 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0013251 dental pulp necrosis IAGP N RGD:5509061 20141003 MGI PMID:10595943 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20150219 MGI PMID:24557836 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0020154 impaired humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:23676465 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0020449 decreased microglial cell activation IAGP N RGD:5509061 20170914 MGI PMID:8673925 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0020854 increased cornea epithelium thickness IAGP N RGD:5509061 20181101 MGI PMID:20713516 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0020950 decreased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200625 MGI PMID:27663205 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0030012 impaired central nervous system regeneration IAGP N RGD:5509061 20170713 MGI PMID:11517251 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:23871670 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:23871670 734247 Tnfrsf1a tumor necrosis factor receptor superfamily, member 1a gene MP:0031118 cardiovalvulitis IAGP N RGD:5509061 20210826 MGI PMID:33210082 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0000745 tremors IEA N RGD:5509061 20170209 MGI 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20170209 MGI PMID:7078649 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0000921 demyelination IAGP N RGD:5509061 20170209 MGI PMID:7078649 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20170209 MGI PMID:15835265 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20170209 MGI PMID:15835265 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20220519 MGI PMID:32160274 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20220519 MGI PMID:32160274 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20170209 MGI PMID:15835265 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20170209 MGI PMID:15835265 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220519 MGI PMID:32160274 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0001263 weight loss IEA N RGD:5509061 20170209 MGI 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170209 MGI PMID:15835265 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20220519 MGI PMID:32160274 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20170209 MGI PMID:7078649 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0002083 premature death IAGP N RGD:5509061 20220519 MGI PMID:32160274 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20170209 MGI PMID:15835265 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0002183 gliosis IAGP N RGD:5509061 20170209 MGI PMID:15835265 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0002183 gliosis IAGP N RGD:5509061 20220519 MGI PMID:32160274 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20170209 MGI PMID:7078649 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0002223 lymphoid hypoplasia IAGP N RGD:5509061 20170209 MGI PMID:7078649 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20220519 MGI PMID:32160274 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20170209 MGI PMID:15835265 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0003444 abnormal neurotransmitter uptake IAGP N RGD:5509061 20170209 MGI PMID:15835265 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20170209 MGI PMID:9756641 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20170209 MGI PMID:15835265 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20220519 MGI PMID:32160274 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20220519 MGI PMID:32160274 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20170209 MGI PMID:7078649 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20170209 MGI PMID:7078649 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20170209 MGI PMID:15835265 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20170209 MGI PMID:7078649 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20170209 MGI PMID:3874230 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20170209 MGI PMID:7078649 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20170209 MGI PMID:7078649 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0009434 paraparesis IEA N RGD:5509061 20170209 MGI 734248 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20220519 MGI PMID:32160274 734249 Rnf38 ring finger protein 38 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 734249 Rnf38 ring finger protein 38 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20161201 MGI 734249 Rnf38 ring finger protein 38 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 734249 Rnf38 ring finger protein 38 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20220811 MGI 734252 Fgb fibrinogen beta chain gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20231207 MGI 734252 Fgb fibrinogen beta chain gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 734252 Fgb fibrinogen beta chain gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 734252 Fgb fibrinogen beta chain gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 734252 Fgb fibrinogen beta chain gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210128 MGI 734252 Fgb fibrinogen beta chain gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 734253 Kmo kynurenine 3-monooxygenase gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20170817 MGI PMID:27754481 734253 Kmo kynurenine 3-monooxygenase gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:24189070 734253 Kmo kynurenine 3-monooxygenase gene MP:0002573 behavioral despair IAGP N RGD:5509061 20170817 MGI PMID:27754481 734253 Kmo kynurenine 3-monooxygenase gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20170817 MGI PMID:27754481 734253 Kmo kynurenine 3-monooxygenase gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:24189070 734253 Kmo kynurenine 3-monooxygenase gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20170817 MGI PMID:27754481 734256 Spag4 sperm associated antigen 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 734256 Spag4 sperm associated antigen 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20161013 MGI PMID:26621829 734256 Spag4 sperm associated antigen 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20220303 MGI PMID:29663073 734256 Spag4 sperm associated antigen 4 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20161013 MGI PMID:26621829 734256 Spag4 sperm associated antigen 4 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20220303 MGI PMID:29663073 734256 Spag4 sperm associated antigen 4 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20161013 MGI PMID:26621829 734256 Spag4 sperm associated antigen 4 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20161013 MGI PMID:26621829 734256 Spag4 sperm associated antigen 4 gene MP:0002686 globozoospermia IAGP N RGD:5509061 20220303 MGI PMID:29663073 734256 Spag4 sperm associated antigen 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220303 MGI PMID:29663073 734256 Spag4 sperm associated antigen 4 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20161013 MGI PMID:26621829 734256 Spag4 sperm associated antigen 4 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220303 MGI PMID:29663073 734256 Spag4 sperm associated antigen 4 gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20220303 MGI PMID:29663073 734256 Spag4 sperm associated antigen 4 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20161013 MGI PMID:26621829 734256 Spag4 sperm associated antigen 4 gene MP:0009231 detached acrosome IAGP N RGD:5509061 20161013 MGI PMID:26621829 734256 Spag4 sperm associated antigen 4 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20161013 MGI PMID:26621829 734256 Spag4 sperm associated antigen 4 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20220303 MGI PMID:29663073 734256 Spag4 sperm associated antigen 4 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20161013 MGI PMID:26621829 734256 Spag4 sperm associated antigen 4 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20161013 MGI PMID:26621829 734256 Spag4 sperm associated antigen 4 gene MP:0009376 abnormal manchette morphology IAGP N RGD:5509061 20220303 MGI PMID:29663073 734256 Spag4 sperm associated antigen 4 gene MP:0009377 ectopic manchette IAGP N RGD:5509061 20220303 MGI PMID:29663073 734256 Spag4 sperm associated antigen 4 gene MP:0009830 abnormal sperm connecting piece morphology IAGP N RGD:5509061 20220303 MGI PMID:29663073 734256 Spag4 sperm associated antigen 4 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20220303 MGI PMID:29663073 734256 Spag4 sperm associated antigen 4 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 734256 Spag4 sperm associated antigen 4 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220303 MGI PMID:29663073 734256 Spag4 sperm associated antigen 4 gene MP:0031374 abnormal manchette assembly IAGP N RGD:5509061 20220428 MGI PMID:26621829 734256 Spag4 sperm associated antigen 4 gene MP:0031388 absent manchette IAGP N RGD:5509061 20220428 MGI PMID:26621829 734257 Stx7 syntaxin 7 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20200514 MGI 734257 Stx7 syntaxin 7 gene MP:0000706 small thymus IEA N RGD:5509061 20200514 MGI 734257 Stx7 syntaxin 7 gene MP:0001565 abnormal circulating phosphate level IEA N RGD:5509061 20211021 MGI 734257 Stx7 syntaxin 7 gene MP:0012361 decreased large unstained cell number IEA N RGD:5509061 20200514 MGI 734259 Slc18a1 solute carrier family 18 (vesicular monoamine), member 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:23201251 734259 Slc18a1 solute carrier family 18 (vesicular monoamine), member 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23201251 734259 Slc18a1 solute carrier family 18 (vesicular monoamine), member 1 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:23201251 734267 Ddx46 DEAD box helicase 46 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 734267 Ddx46 DEAD box helicase 46 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210415 MGI PMID:28846086 734267 Ddx46 DEAD box helicase 46 gene MP:0001727 abnormal embryo implantation IEA N RGD:5509061 20241017 MGI 734267 Ddx46 DEAD box helicase 46 gene MP:0002419 abnormal innate immunity IAGP N RGD:5509061 20210415 MGI PMID:28846086 734267 Ddx46 DEAD box helicase 46 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20210415 MGI PMID:28846086 734267 Ddx46 DEAD box helicase 46 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20221215 MGI 734267 Ddx46 DEAD box helicase 46 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20210415 MGI PMID:28846086 734267 Ddx46 DEAD box helicase 46 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20210415 MGI PMID:28846086 734267 Ddx46 DEAD box helicase 46 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20210415 MGI PMID:28846086 734267 Ddx46 DEAD box helicase 46 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20210415 MGI PMID:28846086 734267 Ddx46 DEAD box helicase 46 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20210415 MGI PMID:28846086 734267 Ddx46 DEAD box helicase 46 gene MP:0011078 increased macrophage cytokine production IAGP N RGD:5509061 20210415 MGI PMID:28846086 734267 Ddx46 DEAD box helicase 46 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210415 MGI PMID:28846086 734267 Ddx46 DEAD box helicase 46 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IEA N RGD:5509061 20241017 MGI 734267 Ddx46 DEAD box helicase 46 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 734267 Ddx46 DEAD box helicase 46 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 734267 Ddx46 DEAD box helicase 46 gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20210415 MGI PMID:28846086 734269 Anxa5 annexin A5 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20151126 MGI PMID:22692895 734269 Anxa5 annexin A5 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17005907 734269 Anxa5 annexin A5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12665588 734269 Anxa5 annexin A5 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17005907 734269 Anxa5 annexin A5 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20151126 MGI PMID:22692895 734269 Anxa5 annexin A5 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20151126 MGI PMID:22692895 734269 Anxa5 annexin A5 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:17005907 734269 Anxa5 annexin A5 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20151126 MGI PMID:22692895 734269 Anxa5 annexin A5 gene MP:0013763 increased T-helper cell number IAGP N RGD:5509061 20151126 MGI PMID:22692895 734271 Fmo3 flavin containing monooxygenase 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 734271 Fmo3 flavin containing monooxygenase 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 734271 Fmo3 flavin containing monooxygenase 3 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210128 MGI 734271 Fmo3 flavin containing monooxygenase 3 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210128 MGI 734271 Fmo3 flavin containing monooxygenase 3 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 734271 Fmo3 flavin containing monooxygenase 3 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 734271 Fmo3 flavin containing monooxygenase 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 734271 Fmo3 flavin containing monooxygenase 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 734271 Fmo3 flavin containing monooxygenase 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 734271 Fmo3 flavin containing monooxygenase 3 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210128 MGI 734271 Fmo3 flavin containing monooxygenase 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20201015 MGI PMID:28636934 734271 Fmo3 flavin containing monooxygenase 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20201015 MGI PMID:28636934 734271 Fmo3 flavin containing monooxygenase 3 gene MP:0020325 abnormal beige fat cell morphology IAGP N RGD:5509061 20201015 MGI PMID:28636934 734273 Mybph myosin binding protein H gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20240523 MGI 734275 Kcnj9 potassium inwardly-rectifying channel, subfamily J, member 9 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 734275 Kcnj9 potassium inwardly-rectifying channel, subfamily J, member 9 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:12040038 734275 Kcnj9 potassium inwardly-rectifying channel, subfamily J, member 9 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12040038 734275 Kcnj9 potassium inwardly-rectifying channel, subfamily J, member 9 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 734275 Kcnj9 potassium inwardly-rectifying channel, subfamily J, member 9 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12040038 734277 Capn6 calpain 6 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:23935533 734277 Capn6 calpain 6 gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23935533 734277 Capn6 calpain 6 gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:23935533 734278 Mgst1 microsomal glutathione S-transferase 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220811 MGI 734278 Mgst1 microsomal glutathione S-transferase 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220811 MGI 734278 Mgst1 microsomal glutathione S-transferase 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20200130 MGI PMID:29702404 734280 Cdk7 cyclin dependent kinase 7 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0009613 thin epidermis suprabasal layer IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0009759 abnormal hair follicle bulge morphology IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0011705 absent fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:22505032 734280 Cdk7 cyclin dependent kinase 7 gene MP:0030927 decreased telomere length IAGP N RGD:5509061 20190117 MGI PMID:22505032 734282 Elf1 E74 like ETS transcription factor 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16002702 734282 Elf1 E74 like ETS transcription factor 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16002702 734283 Uba3 ubiquitin-like modifier activating enzyme 3 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11696557 734283 Uba3 ubiquitin-like modifier activating enzyme 3 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:11696557 734283 Uba3 ubiquitin-like modifier activating enzyme 3 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:11696557 734283 Uba3 ubiquitin-like modifier activating enzyme 3 gene MP:0003693 abnormal blastocyst hatching IAGP N RGD:5509061 20141003 MGI PMID:11696557 734283 Uba3 ubiquitin-like modifier activating enzyme 3 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:11696557 734283 Uba3 ubiquitin-like modifier activating enzyme 3 gene MP:0010380 abnormal inner cell mass apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11696557 734283 Uba3 ubiquitin-like modifier activating enzyme 3 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20111116 MGI 734283 Uba3 ubiquitin-like modifier activating enzyme 3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11696557 734283 Uba3 ubiquitin-like modifier activating enzyme 3 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11696557 734283 Uba3 ubiquitin-like modifier activating enzyme 3 gene MP:0011184 absent embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:11696557 734283 Uba3 ubiquitin-like modifier activating enzyme 3 gene MP:0012128 abnormal blastocyst formation IAGP N RGD:5509061 20141003 MGI PMID:11696557 734285 Mme membrane metallo endopeptidase gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:15615772 734285 Mme membrane metallo endopeptidase gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:11145711 734285 Mme membrane metallo endopeptidase gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20231207 MGI 734285 Mme membrane metallo endopeptidase gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:11145711 734285 Mme membrane metallo endopeptidase gene MP:0005151 diffuse hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:7760013 734285 Mme membrane metallo endopeptidase gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20190523 MGI PMID:27588448 734285 Mme membrane metallo endopeptidase gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:15615772 734285 Mme membrane metallo endopeptidase gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11145711 734285 Mme membrane metallo endopeptidase gene MP:0010738 abnormal internode morphology IAGP N RGD:5509061 20190523 MGI PMID:27588448 734285 Mme membrane metallo endopeptidase gene MP:0011730 increased myelin sheath thickness IAGP N RGD:5509061 20190523 MGI PMID:27588448 734287 Ndufv2 NADH:ubiquinone oxidoreductase core subunit V2 gene MP:0006205 embryonic lethality between implantation and somite formation IEA N RGD:5509061 20141003 MGI 734287 Ndufv2 NADH:ubiquinone oxidoreductase core subunit V2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 734290 F3 coagulation factor III gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15215187 734290 F3 coagulation factor III gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15215187 734290 F3 coagulation factor III gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:8692802 734290 F3 coagulation factor III gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:8781413 734290 F3 coagulation factor III gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:8692802 734290 F3 coagulation factor III gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:8779717 734290 F3 coagulation factor III gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:8692802 734290 F3 coagulation factor III gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9192667 734290 F3 coagulation factor III gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9192667 734290 F3 coagulation factor III gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20200917 MGI PMID:9192667 734290 F3 coagulation factor III gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:8779717 734290 F3 coagulation factor III gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8781413 734290 F3 coagulation factor III gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:12579195 734290 F3 coagulation factor III gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:8779717 734290 F3 coagulation factor III gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:8692802 734290 F3 coagulation factor III gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:8779717 734290 F3 coagulation factor III gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:8781413 734290 F3 coagulation factor III gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:8779717 734290 F3 coagulation factor III gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20201224 MGI PMID:15961065 734290 F3 coagulation factor III gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8692802 734290 F3 coagulation factor III gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9192667 734290 F3 coagulation factor III gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9192667 734290 F3 coagulation factor III gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:9192667 734290 F3 coagulation factor III gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18005233 734290 F3 coagulation factor III gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15961065 734290 F3 coagulation factor III gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15961065 734290 F3 coagulation factor III gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8779717 734290 F3 coagulation factor III gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8779717 734290 F3 coagulation factor III gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9449688 734290 F3 coagulation factor III gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15613025 734290 F3 coagulation factor III gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:14576054 734290 F3 coagulation factor III gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:15215187 734290 F3 coagulation factor III gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:15961065 734290 F3 coagulation factor III gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:8692802 734290 F3 coagulation factor III gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20151203 MGI PMID:24879059 734290 F3 coagulation factor III gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17663739 734290 F3 coagulation factor III gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12579195 734290 F3 coagulation factor III gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:8692802 734290 F3 coagulation factor III gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:8779717 734290 F3 coagulation factor III gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20151203 MGI PMID:24879059 734290 F3 coagulation factor III gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:8692802 734290 F3 coagulation factor III gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:8781413 734290 F3 coagulation factor III gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:15215187 734290 F3 coagulation factor III gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:8692802 734290 F3 coagulation factor III gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:8779717 734290 F3 coagulation factor III gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:8781413 734290 F3 coagulation factor III gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8692802 734290 F3 coagulation factor III gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8781413 734290 F3 coagulation factor III gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20151203 MGI PMID:24879059 734290 F3 coagulation factor III gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8692802 734290 F3 coagulation factor III gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20151203 MGI PMID:24879059 734290 F3 coagulation factor III gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:16020755 734290 F3 coagulation factor III gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15215187 734290 F3 coagulation factor III gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:15961065 734290 F3 coagulation factor III gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:16020755 734290 F3 coagulation factor III gene MP:0006323 abnormal extraembryonic mesoderm development IAGP N RGD:5509061 20151203 MGI PMID:24879059 734290 F3 coagulation factor III gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:15961065 734290 F3 coagulation factor III gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15215187 734290 F3 coagulation factor III gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:15215187 734290 F3 coagulation factor III gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:15215187 734290 F3 coagulation factor III gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:15613025 734290 F3 coagulation factor III gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18005233 734290 F3 coagulation factor III gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15613025 734290 F3 coagulation factor III gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:14576054 734290 F3 coagulation factor III gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:15215187 734290 F3 coagulation factor III gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:14576054 734290 F3 coagulation factor III gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:17363687 734290 F3 coagulation factor III gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:14576054 734290 F3 coagulation factor III gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15215187 734290 F3 coagulation factor III gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:15215187 734290 F3 coagulation factor III gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9192667 734290 F3 coagulation factor III gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15961065 734290 F3 coagulation factor III gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15956290 734290 F3 coagulation factor III gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8781413 734290 F3 coagulation factor III gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12579195 734290 F3 coagulation factor III gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8692802 734290 F3 coagulation factor III gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8779717 734290 F3 coagulation factor III gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9192667 734290 F3 coagulation factor III gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20151203 MGI PMID:24879059 734290 F3 coagulation factor III gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8781413 734290 F3 coagulation factor III gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9192667 734290 F3 coagulation factor III gene MP:0012329 increased circulating factor VIII level IAGP N RGD:5509061 20210204 MGI PMID:15961065 734290 F3 coagulation factor III gene MP:0012358 decreased partial thromboplastin time IAGP N RGD:5509061 20201001 MGI PMID:15961065 734290 F3 coagulation factor III gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:12579195 734290 F3 coagulation factor III gene MP:0012616 increased circulating factor IX level IAGP N RGD:5509061 20210204 MGI PMID:15961065 734290 F3 coagulation factor III gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:8692802 734290 F3 coagulation factor III gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:8779717 734290 F3 coagulation factor III gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:15215187 734290 F3 coagulation factor III gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20201224 MGI PMID:15961065 734290 F3 coagulation factor III gene MP:0020985 increased circulating factor XI level IAGP N RGD:5509061 20210204 MGI PMID:15961065 734290 F3 coagulation factor III gene MP:0030975 placenta hemorrhage IAGP N RGD:5509061 20191010 MGI PMID:12579195 734290 F3 coagulation factor III gene MP:0031147 abnormal ventricular thrombosis IAGP N RGD:5509061 20201224 MGI PMID:15961065 734290 F3 coagulation factor III gene MP:0031510 increased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:16020755 734294 Ptgfr prostaglandin F receptor gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:9235889 734294 Ptgfr prostaglandin F receptor gene MP:0002783 abnormal ovary secretion IAGP N RGD:5509061 20141003 MGI PMID:9235889 734294 Ptgfr prostaglandin F receptor gene MP:0012010 parturition failure IAGP N RGD:5509061 20141003 MGI PMID:12606450 734294 Ptgfr prostaglandin F receptor gene MP:0012010 parturition failure IAGP N RGD:5509061 20141003 MGI PMID:9235889 734296 Rab38 RAB38, member RAS oncogene family gene MP:0000371 diluted coat color IAGP N RGD:5509061 20210121 MGI PMID:31399401 734296 Rab38 RAB38, member RAS oncogene family gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20210121 MGI PMID:31399401 734296 Rab38 RAB38, member RAS oncogene family gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11917121 734296 Rab38 RAB38, member RAS oncogene family gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20141003 MGI PMID:18832574 734296 Rab38 RAB38, member RAS oncogene family gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11917121 734296 Rab38 RAB38, member RAS oncogene family gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18832574 734296 Rab38 RAB38, member RAS oncogene family gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:22660928 734296 Rab38 RAB38, member RAS oncogene family gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:23426636 734296 Rab38 RAB38, member RAS oncogene family gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11917121 734296 Rab38 RAB38, member RAS oncogene family gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18832574 734296 Rab38 RAB38, member RAS oncogene family gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18832574 734296 Rab38 RAB38, member RAS oncogene family gene MP:0004382 abnormal hair follicle melanogenesis IAGP N RGD:5509061 20141003 MGI PMID:18832574 734296 Rab38 RAB38, member RAS oncogene family gene MP:0004721 abnormal platelet dense granule morphology IAGP N RGD:5509061 20210121 MGI PMID:31399401 734296 Rab38 RAB38, member RAS oncogene family gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20210121 MGI PMID:31399401 734296 Rab38 RAB38, member RAS oncogene family gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:18832574 734296 Rab38 RAB38, member RAS oncogene family gene MP:0005075 abnormal melanosome morphology IAGP N RGD:5509061 20141003 MGI PMID:11917121 734296 Rab38 RAB38, member RAS oncogene family gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18715234 734296 Rab38 RAB38, member RAS oncogene family gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18832574 734296 Rab38 RAB38, member RAS oncogene family gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20210121 MGI PMID:31399401 734296 Rab38 RAB38, member RAS oncogene family gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20210121 MGI PMID:31399401 734296 Rab38 RAB38, member RAS oncogene family gene MP:0009448 decreased platelet ATP level IAGP N RGD:5509061 20210121 MGI PMID:31399401 734296 Rab38 RAB38, member RAS oncogene family gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20210121 MGI PMID:31399401 734296 Rab38 RAB38, member RAS oncogene family gene MP:0009557 decreased platelet ADP level IAGP N RGD:5509061 20210121 MGI PMID:31399401 734296 Rab38 RAB38, member RAS oncogene family gene MP:0010815 enlarged alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:18832574 734296 Rab38 RAB38, member RAS oncogene family gene MP:0010815 enlarged alveolar lamellar bodies IAGP N RGD:5509061 20210121 MGI PMID:31399401 734296 Rab38 RAB38, member RAS oncogene family gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:18832574 734296 Rab38 RAB38, member RAS oncogene family gene MP:0010891 increased alveolar lamellar body number IAGP N RGD:5509061 20141003 MGI PMID:18832574 734296 Rab38 RAB38, member RAS oncogene family gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:18832574 734296 Rab38 RAB38, member RAS oncogene family gene MP:0010903 abnormal pulmonary alveolus wall morphology IAGP N RGD:5509061 20141003 MGI PMID:18832574 734296 Rab38 RAB38, member RAS oncogene family gene MP:0010908 dilated pulmonary alveolar duct IAGP N RGD:5509061 20141003 MGI PMID:18832574 734296 Rab38 RAB38, member RAS oncogene family gene MP:0010911 abnormal pulmonary acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:18832574 734296 Rab38 RAB38, member RAS oncogene family gene MP:0010911 abnormal pulmonary acinus morphology IAGP N RGD:5509061 20210121 MGI PMID:31399401 734296 Rab38 RAB38, member RAS oncogene family gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20210121 MGI PMID:31399401 734296 Rab38 RAB38, member RAS oncogene family gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20210121 MGI PMID:31399401 734298 Psmd4 proteasome (prosome, macropain) 26S subunit, non-ATPase, 4 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:17646385 734298 Psmd4 proteasome (prosome, macropain) 26S subunit, non-ATPase, 4 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:17646385 734298 Psmd4 proteasome (prosome, macropain) 26S subunit, non-ATPase, 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17646385 734298 Psmd4 proteasome (prosome, macropain) 26S subunit, non-ATPase, 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17646385 734298 Psmd4 proteasome (prosome, macropain) 26S subunit, non-ATPase, 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17646385 734298 Psmd4 proteasome (prosome, macropain) 26S subunit, non-ATPase, 4 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17646385 734298 Psmd4 proteasome (prosome, macropain) 26S subunit, non-ATPase, 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17646385 734298 Psmd4 proteasome (prosome, macropain) 26S subunit, non-ATPase, 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17646385 734298 Psmd4 proteasome (prosome, macropain) 26S subunit, non-ATPase, 4 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:17646385 734300 Bcl2l11 BCL2 like 11 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19651893 734300 Bcl2l11 BCL2 like 11 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22081075 734300 Bcl2l11 BCL2 like 11 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20190919 MGI PMID:27525555 734300 Bcl2l11 BCL2 like 11 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:11709185 734300 Bcl2l11 BCL2 like 11 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:19651893 734300 Bcl2l11 BCL2 like 11 gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20141003 MGI PMID:11709185 734300 Bcl2l11 BCL2 like 11 gene MP:0000571 interdigital webbing IAGP N RGD:5509061 20141003 MGI PMID:19841067 734300 Bcl2l11 BCL2 like 11 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:14635229 734300 Bcl2l11 BCL2 like 11 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22891272 734300 Bcl2l11 BCL2 like 11 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19841067 734300 Bcl2l11 BCL2 like 11 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:16780816 734300 Bcl2l11 BCL2 like 11 gene MP:0001025 abnormal sympathetic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17535852 734300 Bcl2l11 BCL2 like 11 gene MP:0001144 vagina atresia IAGP N RGD:5509061 20141003 MGI PMID:19841067 734300 Bcl2l11 BCL2 like 11 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19841067 734300 Bcl2l11 BCL2 like 11 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19651893 734300 Bcl2l11 BCL2 like 11 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22081075 734300 Bcl2l11 BCL2 like 11 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22081075 734300 Bcl2l11 BCL2 like 11 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11709185 734300 Bcl2l11 BCL2 like 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19651893 734300 Bcl2l11 BCL2 like 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22081075 734300 Bcl2l11 BCL2 like 11 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22117047 734300 Bcl2l11 BCL2 like 11 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11709185 734300 Bcl2l11 BCL2 like 11 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:16780816 734300 Bcl2l11 BCL2 like 11 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16055554 734300 Bcl2l11 BCL2 like 11 gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16055554 734300 Bcl2l11 BCL2 like 11 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16055554 734300 Bcl2l11 BCL2 like 11 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18454133 734300 Bcl2l11 BCL2 like 11 gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20230119 MGI 734300 Bcl2l11 BCL2 like 11 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 734300 Bcl2l11 BCL2 like 11 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0003537 hydrometrocolpos IAGP N RGD:5509061 20141003 MGI PMID:19841067 734300 Bcl2l11 BCL2 like 11 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11709185 734300 Bcl2l11 BCL2 like 11 gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11709185 734300 Bcl2l11 BCL2 like 11 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18287039 734300 Bcl2l11 BCL2 like 11 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18299399 734300 Bcl2l11 BCL2 like 11 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19651893 734300 Bcl2l11 BCL2 like 11 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22891272 734300 Bcl2l11 BCL2 like 11 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23805138 734300 Bcl2l11 BCL2 like 11 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20190919 MGI PMID:27525555 734300 Bcl2l11 BCL2 like 11 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20230119 MGI 734300 Bcl2l11 BCL2 like 11 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 734300 Bcl2l11 BCL2 like 11 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18287039 734300 Bcl2l11 BCL2 like 11 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19841067 734300 Bcl2l11 BCL2 like 11 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 734300 Bcl2l11 BCL2 like 11 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18454133 734300 Bcl2l11 BCL2 like 11 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18329371 734300 Bcl2l11 BCL2 like 11 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17618288 734300 Bcl2l11 BCL2 like 11 gene MP:0005068 abnormal NK cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17618288 734300 Bcl2l11 BCL2 like 11 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15210829 734300 Bcl2l11 BCL2 like 11 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11709185 734300 Bcl2l11 BCL2 like 11 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 734300 Bcl2l11 BCL2 like 11 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20230119 MGI 734300 Bcl2l11 BCL2 like 11 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17618288 734300 Bcl2l11 BCL2 like 11 gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20161013 MGI PMID:27044867 734300 Bcl2l11 BCL2 like 11 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:18327259 734300 Bcl2l11 BCL2 like 11 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11709185 734300 Bcl2l11 BCL2 like 11 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11709185 734300 Bcl2l11 BCL2 like 11 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18299399 734300 Bcl2l11 BCL2 like 11 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19841067 734300 Bcl2l11 BCL2 like 11 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:23623381 734300 Bcl2l11 BCL2 like 11 gene MP:0008044 increased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:17618288 734300 Bcl2l11 BCL2 like 11 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:22201126 734300 Bcl2l11 BCL2 like 11 gene MP:0008073 abnormal CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18287039 734300 Bcl2l11 BCL2 like 11 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19841067 734300 Bcl2l11 BCL2 like 11 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19841067 734300 Bcl2l11 BCL2 like 11 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:22117047 734300 Bcl2l11 BCL2 like 11 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 734300 Bcl2l11 BCL2 like 11 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:18327259 734300 Bcl2l11 BCL2 like 11 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:22117047 734300 Bcl2l11 BCL2 like 11 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 734300 Bcl2l11 BCL2 like 11 gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0008189 increased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18299399 734300 Bcl2l11 BCL2 like 11 gene MP:0008206 increased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16055554 734300 Bcl2l11 BCL2 like 11 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18299399 734300 Bcl2l11 BCL2 like 11 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18329371 734300 Bcl2l11 BCL2 like 11 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18299399 734300 Bcl2l11 BCL2 like 11 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:22891272 734300 Bcl2l11 BCL2 like 11 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:19651893 734300 Bcl2l11 BCL2 like 11 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11709185 734300 Bcl2l11 BCL2 like 11 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15210829 734300 Bcl2l11 BCL2 like 11 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18287039 734300 Bcl2l11 BCL2 like 11 gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17618288 734300 Bcl2l11 BCL2 like 11 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:23717580 734300 Bcl2l11 BCL2 like 11 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0009338 increased splenocyte number IAGP N RGD:5509061 20141003 MGI PMID:19841067 734300 Bcl2l11 BCL2 like 11 gene MP:0009341 decreased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19651893 734300 Bcl2l11 BCL2 like 11 gene MP:0009341 decreased splenocyte apoptosis IAGP N RGD:5509061 20190103 MGI PMID:26563351 734300 Bcl2l11 BCL2 like 11 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:14635229 734300 Bcl2l11 BCL2 like 11 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20150212 MGI PMID:18498746 734300 Bcl2l11 BCL2 like 11 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20190103 MGI PMID:26563351 734300 Bcl2l11 BCL2 like 11 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20230601 MGI 734300 Bcl2l11 BCL2 like 11 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230119 MGI 734300 Bcl2l11 BCL2 like 11 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19841067 734300 Bcl2l11 BCL2 like 11 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0011369 increased renal glomerulus apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18275831 734300 Bcl2l11 BCL2 like 11 gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16270031 734300 Bcl2l11 BCL2 like 11 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20230119 MGI 734300 Bcl2l11 BCL2 like 11 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20160414 MGI PMID:26832406 734300 Bcl2l11 BCL2 like 11 gene MP:0013023 decreased Ly6C high monocyte number IAGP N RGD:5509061 20190919 MGI PMID:27525555 734300 Bcl2l11 BCL2 like 11 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:18498746 734300 Bcl2l11 BCL2 like 11 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:10576740 734300 Bcl2l11 BCL2 like 11 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:16270031 734302 Serpina5 serine (or cysteine) peptidase inhibitor, clade A, member 5 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11120760 734302 Serpina5 serine (or cysteine) peptidase inhibitor, clade A, member 5 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11120760 734302 Serpina5 serine (or cysteine) peptidase inhibitor, clade A, member 5 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:11120760 734302 Serpina5 serine (or cysteine) peptidase inhibitor, clade A, member 5 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 734302 Serpina5 serine (or cysteine) peptidase inhibitor, clade A, member 5 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11120760 734302 Serpina5 serine (or cysteine) peptidase inhibitor, clade A, member 5 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20230601 MGI 734302 Serpina5 serine (or cysteine) peptidase inhibitor, clade A, member 5 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11120760 734302 Serpina5 serine (or cysteine) peptidase inhibitor, clade A, member 5 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11120760 734302 Serpina5 serine (or cysteine) peptidase inhibitor, clade A, member 5 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20201022 MGI 734302 Serpina5 serine (or cysteine) peptidase inhibitor, clade A, member 5 gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11120760 734302 Serpina5 serine (or cysteine) peptidase inhibitor, clade A, member 5 gene MP:0005410 abnormal fertilization IAGP N RGD:5509061 20141003 MGI PMID:11120760 734302 Serpina5 serine (or cysteine) peptidase inhibitor, clade A, member 5 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11120760 734304 Siah2 siah E3 ubiquitin protein ligase 2 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:14645526 734304 Siah2 siah E3 ubiquitin protein ligase 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14645526 734304 Siah2 siah E3 ubiquitin protein ligase 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14645526 734304 Siah2 siah E3 ubiquitin protein ligase 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14645526 734304 Siah2 siah E3 ubiquitin protein ligase 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14645526 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:15798219 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:15798219 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10944538 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10944538 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:15798219 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0004781 abnormal surfactant composition IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:15798219 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0010811 decreased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0010890 decreased alveolar lamellar body number IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0011018 pulmonary hyaline membrane formation IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17130238 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15798219 734305 Pcyt1a phosphate cytidylyltransferase 1, choline, alpha isoform gene MP:0014473 increased pulmonary alveolus wall thickness IAGP N RGD:5509061 20240704 MGI PMID:17130238 734310 Ackr3 atypical chemokine receptor 3 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0000275 heart hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18442043 734310 Ackr3 atypical chemokine receptor 3 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0000281 abnormal interventricular septum morphology IEA N RGD:5509061 20111116 MGI 734310 Ackr3 atypical chemokine receptor 3 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20231221 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0000745 tremors IEA N RGD:5509061 20201231 MGI 734310 Ackr3 atypical chemokine receptor 3 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23395391 734310 Ackr3 atypical chemokine receptor 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:18442043 734310 Ackr3 atypical chemokine receptor 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18442043 734310 Ackr3 atypical chemokine receptor 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18442043 734310 Ackr3 atypical chemokine receptor 3 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:18442043 734310 Ackr3 atypical chemokine receptor 3 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 734310 Ackr3 atypical chemokine receptor 3 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18442043 734310 Ackr3 atypical chemokine receptor 3 gene MP:0006116 calcified aortic valve IAGP N RGD:5509061 20141003 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18442043 734310 Ackr3 atypical chemokine receptor 3 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160811 MGI 734310 Ackr3 atypical chemokine receptor 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0010426 abnormal heart and great artery attachment IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20231221 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0010527 bicuspid pulmonary valve IAGP N RGD:5509061 20231221 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20231221 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0010595 abnormal aortic valve cusp morphology IAGP N RGD:5509061 20231221 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0010596 unicuspid aortic valve IAGP N RGD:5509061 20231221 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0010602 abnormal pulmonary valve cusp morphology IAGP N RGD:5509061 20231221 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0010603 unicuspid pulmonary valve IAGP N RGD:5509061 20231221 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0010605 thick pulmonary valve cusps IAGP N RGD:5509061 20231221 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18442043 734310 Ackr3 atypical chemokine receptor 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17804806 734310 Ackr3 atypical chemokine receptor 3 gene MP:0011089 perinatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 734310 Ackr3 atypical chemokine receptor 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21246655 734310 Ackr3 atypical chemokine receptor 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 734310 Ackr3 atypical chemokine receptor 3 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 734310 Ackr3 atypical chemokine receptor 3 gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:21246655 734313 Echs1 enoyl Coenzyme A hydratase, short chain, 1, mitochondrial gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20201015 MGI PMID:31690668 734313 Echs1 enoyl Coenzyme A hydratase, short chain, 1, mitochondrial gene MP:0002764 short tibia IEA N RGD:5509061 20240523 MGI 734313 Echs1 enoyl Coenzyme A hydratase, short chain, 1, mitochondrial gene MP:0010358 abnormal free fatty acids level IAGP N RGD:5509061 20201015 MGI PMID:31690668 734313 Echs1 enoyl Coenzyme A hydratase, short chain, 1, mitochondrial gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20201015 MGI PMID:31690668 734315 Atp5mc3 ATP synthase membrane subunit c locus 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230720 MGI 734316 Stc1 stanniocalcin 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18258678 734316 Stc1 stanniocalcin 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18258678 734316 Stc1 stanniocalcin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16287871 734317 Fgf23 fibroblast growth factor 23 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0000132 thickened long bone epiphysis IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20150319 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0000167 decreased chondrocyte number IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:22006328 734317 Fgf23 fibroblast growth factor 23 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:21427221 734317 Fgf23 fibroblast growth factor 23 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21427221 734317 Fgf23 fibroblast growth factor 23 gene MP:0001562 abnormal circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0001565 abnormal circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:21427221 734317 Fgf23 fibroblast growth factor 23 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:21427221 734317 Fgf23 fibroblast growth factor 23 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21427221 734317 Fgf23 fibroblast growth factor 23 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:22006328 734317 Fgf23 fibroblast growth factor 23 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:21427221 734317 Fgf23 fibroblast growth factor 23 gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22006328 734317 Fgf23 fibroblast growth factor 23 gene MP:0004348 long femur IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0004348 long femur IAGP N RGD:5509061 20181011 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0005265 abnormal blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20141003 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0005636 abnormal mineral homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0006133 calcified artery IAGP N RGD:5509061 20141003 MGI PMID:21427221 734317 Fgf23 fibroblast growth factor 23 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0009445 osteomalacia IAGP N RGD:5509061 20141003 MGI PMID:22006328 734317 Fgf23 fibroblast growth factor 23 gene MP:0010110 abnormal renal phosphate reabsorption IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:15579309 734317 Fgf23 fibroblast growth factor 23 gene MP:0010924 abnormal osteoid morphology IAGP N RGD:5509061 20141003 MGI PMID:22006328 734317 Fgf23 fibroblast growth factor 23 gene MP:0010929 increased osteoid thickness IAGP N RGD:5509061 20141003 MGI PMID:22006328 734317 Fgf23 fibroblast growth factor 23 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:14966565 734317 Fgf23 fibroblast growth factor 23 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:16449303 734317 Fgf23 fibroblast growth factor 23 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:22006328 734317 Fgf23 fibroblast growth factor 23 gene MP:0013616 decreased volumetric bone mineral density IAGP N RGD:5509061 20150319 MGI PMID:17123805 734317 Fgf23 fibroblast growth factor 23 gene MP:0013616 decreased volumetric bone mineral density IAGP N RGD:5509061 20220915 MGI PMID:15579309 734319 Tpp2 tripeptidyl peptidase II gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20151217 MGI PMID:25414442 734319 Tpp2 tripeptidyl peptidase II gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20151217 MGI PMID:25414442 734319 Tpp2 tripeptidyl peptidase II gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20151217 MGI PMID:25414442 734319 Tpp2 tripeptidyl peptidase II gene MP:0000716 abnormal immune system cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0001835 abnormal antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:19841172 734319 Tpp2 tripeptidyl peptidase II gene MP:0001839 abnormal level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:19841172 734319 Tpp2 tripeptidyl peptidase II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20151217 MGI PMID:25414442 734319 Tpp2 tripeptidyl peptidase II gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20151217 MGI PMID:25414442 734319 Tpp2 tripeptidyl peptidase II gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20151217 MGI PMID:25414442 734319 Tpp2 tripeptidyl peptidase II gene MP:0005014 increased B cell number IAGP N RGD:5509061 20151217 MGI PMID:25414442 734319 Tpp2 tripeptidyl peptidase II gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20151217 MGI PMID:25414442 734319 Tpp2 tripeptidyl peptidase II gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20151217 MGI PMID:25414442 734319 Tpp2 tripeptidyl peptidase II gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20151217 MGI PMID:25414442 734319 Tpp2 tripeptidyl peptidase II gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:18362329 734319 Tpp2 tripeptidyl peptidase II gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18362329 734322 Lin7b lin-7 homolog B, crumbs cell polarity complex component gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:16186258 734322 Lin7b lin-7 homolog B, crumbs cell polarity complex component gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11104771 734322 Lin7b lin-7 homolog B, crumbs cell polarity complex component gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16186258 734322 Lin7b lin-7 homolog B, crumbs cell polarity complex component gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16186258 734322 Lin7b lin-7 homolog B, crumbs cell polarity complex component gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16186258 734324 Mxd3 Max dimerization protein 3 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:11154258 734324 Mxd3 Max dimerization protein 3 gene MP:0009084 blind uterus IEA N RGD:5509061 20210826 MGI 734328 Adam18 a disintegrin and metallopeptidase domain 18 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180830 MGI PMID:27357688 734328 Adam18 a disintegrin and metallopeptidase domain 18 gene MP:0003858 enhanced coordination IEA N RGD:5509061 20141003 MGI 734331 P2rx5 purinergic receptor P2X, ligand-gated ion channel, 5 gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 734331 P2rx5 purinergic receptor P2X, ligand-gated ion channel, 5 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20141003 MGI 734331 P2rx5 purinergic receptor P2X, ligand-gated ion channel, 5 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 734331 P2rx5 purinergic receptor P2X, ligand-gated ion channel, 5 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20141003 MGI 734331 P2rx5 purinergic receptor P2X, ligand-gated ion channel, 5 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20141003 MGI 734331 P2rx5 purinergic receptor P2X, ligand-gated ion channel, 5 gene MP:0009456 impaired cued conditioning behavior IEA N RGD:5509061 20141003 MGI 734331 P2rx5 purinergic receptor P2X, ligand-gated ion channel, 5 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:24355923 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11070163 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12091349 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18029401 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000274 enlarged heart IEA N RGD:5509061 20200514 MGI 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:12091349 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20200514 MGI 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000601 small liver IEA N RGD:5509061 20200514 MGI 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000678 abnormal parathyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000680 absent parathyroid glands IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12091349 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:12091349 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:12091349 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:21911454 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:12091349 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12091349 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:12091349 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:18029401 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:18029401 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:8873772 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11070163 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18821589 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:18821589 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12091349 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:12091349 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:12091349 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18821589 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001861 lung inflammation IAGP N RGD:5509061 20171207 MGI PMID:27864286 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:12091349 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:12091349 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0001889 delayed brain development IAGP N RGD:5509061 20141003 MGI PMID:18029401 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21911454 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16780827 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20181122 MGI PMID:20144786 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12091349 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19520971 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21911454 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24355923 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11857781 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12091349 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17911384 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16780827 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:18990706 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11070163 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11070163 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11070163 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:24278477 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20141003 MGI PMID:24278477 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16332365 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:24278477 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:19520971 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:18029401 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0002981 increased liver weight IAGP N RGD:5509061 20170601 MGI PMID:26699479 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003068 enlarged kidney IEA N RGD:5509061 20200514 MGI 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:24496627 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003099 retina detachment IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:18990706 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003154 abnormal soft palate morphology IAGP N RGD:5509061 20141003 MGI PMID:24496627 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:24355923 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15548578 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18029401 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:8873772 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20170601 MGI PMID:26699479 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8873772 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003494 parathyroid hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003756 abnormal hard palate morphology IAGP N RGD:5509061 20141003 MGI PMID:16780827 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11559531 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18029401 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8873772 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004044 aortic dissection IAGP N RGD:5509061 20141003 MGI PMID:24355923 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:24355923 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16332365 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:24355923 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:16332365 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20141003 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20181122 MGI PMID:20144786 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11559531 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004540 small maxilla IAGP N RGD:5509061 20141003 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004551 decreased tracheal cartilage ring number IAGP N RGD:5509061 20141003 MGI PMID:18990706 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16332365 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004913 absent mandibular angle IAGP N RGD:5509061 20141003 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004940 abnormal B-1 B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11070163 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:24115907 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0004976 abnormal B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:11070163 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21911454 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21911454 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0005039 hypoxia IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19520971 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:24355923 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:24355923 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19270708 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:18029401 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:19270708 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20171207 MGI PMID:27864286 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0006185 retina hemorrhage IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0006202 vitreous body hemorrhage IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16332365 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:24115907 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0008100 absent plasma cells IAGP N RGD:5509061 20141003 MGI PMID:11070163 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0008119 decreased Langerhans cell number IAGP N RGD:5509061 20141003 MGI PMID:17938236 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0008136 enlarged Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:11070163 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21911454 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0008712 decreased interleukin-9 secretion IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0008918 microgliosis IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009025 abnormal brain dura mater morphology IAGP N RGD:5509061 20141003 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009057 increased interleukin-21 secretion IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22904682 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22904682 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009343 dilated gallbladder IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:24496627 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:16780827 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009625 abnormal abdominal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:23569233 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20141003 MGI PMID:16780827 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009654 abnormal primary palate development IAGP N RGD:5509061 20141003 MGI PMID:16780827 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009845 abnormal neural crest cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:16780827 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16780827 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:19270708 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0010037 ectopic melanocytes IAGP N RGD:5509061 20181122 MGI PMID:20144786 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0010206 pigment incontinence IAGP N RGD:5509061 20181129 MGI PMID:20144786 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16332365 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0010452 retina microaneurysm IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0010464 abnormal aortic arch and aortic arch branch attachment IAGP N RGD:5509061 20141003 MGI PMID:15741317 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0010661 ascending aorta aneurysm IAGP N RGD:5509061 20141003 MGI PMID:24355923 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0010668 abnormal hepatic portal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:18990706 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:18990706 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0010988 abnormal bronchial cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:18990706 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20141003 MGI PMID:24355923 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:18990706 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16332365 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18821589 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15548578 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18029401 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8873772 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18029401 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18990706 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11857781 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0011572 abnormal aorta bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:24355923 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0011575 dilated aorta bulb IAGP N RGD:5509061 20141003 MGI PMID:24355923 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0011659 interrupted aortic arch, type b IAGP N RGD:5509061 20231214 MGI PMID:16332365 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0011830 ectopic hair follicle melanin granules IAGP N RGD:5509061 20181122 MGI PMID:20144786 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:18029401 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20151015 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0012236 abnormal cholangiocyte morphology IAGP N RGD:5509061 20170601 MGI PMID:26699479 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0012760 decreased cranial neural crest cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0013184 hemorrhagic ascites IAGP N RGD:5509061 20141003 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0013546 cleft soft palate IAGP N RGD:5509061 20171102 MGI PMID:24496627 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:25857227 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0030224 abnormal soft palate muscle morphology IAGP N RGD:5509061 20171019 MGI PMID:24496627 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0030258 small mandibular condyloid process IAGP N RGD:5509061 20171019 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0030283 small mandibular coronoid process IAGP N RGD:5509061 20171102 MGI PMID:12975342 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0030293 small tensor veli palatini muscle IAGP N RGD:5509061 20171102 MGI PMID:24496627 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0030295 small levator veli palatini muscle IAGP N RGD:5509061 20171102 MGI PMID:24496627 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20171221 MGI PMID:24278477 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0030459 abnormal tooth attrition IAGP N RGD:5509061 20171221 MGI PMID:24278477 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0031159 abnormal hepatic portal vein thrombosis IAGP N RGD:5509061 20201210 MGI PMID:17114585 734333 Tgfbr2 transforming growth factor, beta receptor II gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:16780827 734335 Cpn1 carboxypeptidase N, polypeptide 1 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20220811 MGI 734335 Cpn1 carboxypeptidase N, polypeptide 1 gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:19414808 734335 Cpn1 carboxypeptidase N, polypeptide 1 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:19414808 734335 Cpn1 carboxypeptidase N, polypeptide 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 734336 Cd86 CD86 antigen gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12207354 734336 Cd86 CD86 antigen gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9075931 734336 Cd86 CD86 antigen gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:19050296 734336 Cd86 CD86 antigen gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:11535635 734336 Cd86 CD86 antigen gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:11535635 734336 Cd86 CD86 antigen gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11535635 734336 Cd86 CD86 antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:9075931 734336 Cd86 CD86 antigen gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:9075931 734336 Cd86 CD86 antigen gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:10477557 734336 Cd86 CD86 antigen gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:11535635 734336 Cd86 CD86 antigen gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20141003 MGI PMID:9075931 734336 Cd86 CD86 antigen gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10453003 734336 Cd86 CD86 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9075931 734336 Cd86 CD86 antigen gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:10453003 734336 Cd86 CD86 antigen gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:10795741 734336 Cd86 CD86 antigen gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:11535635 734336 Cd86 CD86 antigen gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:19050296 734336 Cd86 CD86 antigen gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:11535635 734336 Cd86 CD86 antigen gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:11535635 734336 Cd86 CD86 antigen gene MP:0003994 abnormal dorsal spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:11535635 734336 Cd86 CD86 antigen gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:10795741 734336 Cd86 CD86 antigen gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:16886063 734336 Cd86 CD86 antigen gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12207354 734336 Cd86 CD86 antigen gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:10477557 734336 Cd86 CD86 antigen gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12207354 734336 Cd86 CD86 antigen gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:10795741 734336 Cd86 CD86 antigen gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:15467837 734336 Cd86 CD86 antigen gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:16886063 734336 Cd86 CD86 antigen gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:11535635 734336 Cd86 CD86 antigen gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:16886063 734336 Cd86 CD86 antigen gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:15467837 734336 Cd86 CD86 antigen gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16886063 734336 Cd86 CD86 antigen gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23793062 734336 Cd86 CD86 antigen gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10725709 734336 Cd86 CD86 antigen gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10453003 734336 Cd86 CD86 antigen gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19050296 734336 Cd86 CD86 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10477557 734336 Cd86 CD86 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15467837 734336 Cd86 CD86 antigen gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10453003 734336 Cd86 CD86 antigen gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:11535635 734336 Cd86 CD86 antigen gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:11535635 734336 Cd86 CD86 antigen gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:19050296 734336 Cd86 CD86 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10795741 734336 Cd86 CD86 antigen gene MP:0005623 abnormal meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:12207354 734336 Cd86 CD86 antigen gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:10725709 734336 Cd86 CD86 antigen gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:9075931 734336 Cd86 CD86 antigen gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9075931 734336 Cd86 CD86 antigen gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9075931 734336 Cd86 CD86 antigen gene MP:0008502 increased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9075931 734336 Cd86 CD86 antigen gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:10477557 734336 Cd86 CD86 antigen gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19917682 734336 Cd86 CD86 antigen gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10477557 734336 Cd86 CD86 antigen gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19050296 734336 Cd86 CD86 antigen gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:19917682 734336 Cd86 CD86 antigen gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:12207354 734336 Cd86 CD86 antigen gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:16200068 734336 Cd86 CD86 antigen gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:19050296 734336 Cd86 CD86 antigen gene MP:0009023 abnormal spinal cord meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:12207354 734336 Cd86 CD86 antigen gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19050296 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:15750601 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17571162 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:15750601 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:11449275 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:11861309 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:21653832 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17571162 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11861309 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0002764 short tibia IEA N RGD:5509061 20210520 MGI 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17571162 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:17571162 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17571162 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:17571162 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:17571162 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:17571162 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:15750601 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:15750601 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:15750601 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17353274 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17571162 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0005462 abnormal mast cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11861309 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11449275 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:21653832 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:15750601 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:17571162 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:15750601 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:11449275 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:21653832 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:17571162 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20141003 MGI PMID:15750601 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0010961 increased compact bone mass IAGP N RGD:5509061 20141003 MGI PMID:15750601 734338 Gab2 growth factor receptor bound protein 2-associated protein 2 gene MP:0020935 decreased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:16314834 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16174787 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16174787 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16174787 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0001079 absent phrenic nerve IAGP N RGD:5509061 20141003 MGI PMID:16174787 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:16174787 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16174787 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12582158 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:16174787 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12582158 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:16174787 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12582158 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:12582158 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12582158 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0002321 hypoventilation IAGP N RGD:5509061 20141003 MGI PMID:12582158 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:16174787 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:16174787 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12582158 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16174787 734340 Slc5a3 solute carrier family 5 (inositol transporters), member 3 gene MP:0012172 abnormal amniotic fluid composition IAGP N RGD:5509061 20141003 MGI PMID:12582158 734341 Myoc myocilin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151203 MGI PMID:11604506 734341 Myoc myocilin gene MP:0005257 abnormal intraocular pressure IAGP N RGD:5509061 20141003 MGI PMID:16954374 734344 Itga7 integrin alpha 7 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:15252120 734344 Itga7 integrin alpha 7 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:15252120 734344 Itga7 integrin alpha 7 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:9354797 734344 Itga7 integrin alpha 7 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:16003770 734344 Itga7 integrin alpha 7 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:9354797 734344 Itga7 integrin alpha 7 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12588796 734344 Itga7 integrin alpha 7 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9354797 734344 Itga7 integrin alpha 7 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:24227711 734344 Itga7 integrin alpha 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:15252120 734344 Itga7 integrin alpha 7 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15252120 734344 Itga7 integrin alpha 7 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:15252120 734344 Itga7 integrin alpha 7 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16003770 734344 Itga7 integrin alpha 7 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15252120 734344 Itga7 integrin alpha 7 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16003770 734344 Itga7 integrin alpha 7 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16003770 734344 Itga7 integrin alpha 7 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:9354797 734344 Itga7 integrin alpha 7 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:24227711 734344 Itga7 integrin alpha 7 gene MP:0002975 vascular smooth muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16003770 734344 Itga7 integrin alpha 7 gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9354797 734344 Itga7 integrin alpha 7 gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:24227711 734344 Itga7 integrin alpha 7 gene MP:0005489 vascular smooth muscle hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16003770 734344 Itga7 integrin alpha 7 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16003770 734344 Itga7 integrin alpha 7 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15252120 734344 Itga7 integrin alpha 7 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15252120 734344 Itga7 integrin alpha 7 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:9354797 734344 Itga7 integrin alpha 7 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:9354797 734344 Itga7 integrin alpha 7 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:9354797 734344 Itga7 integrin alpha 7 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:9354797 734344 Itga7 integrin alpha 7 gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141003 MGI PMID:24227711 734344 Itga7 integrin alpha 7 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:9354797 734344 Itga7 integrin alpha 7 gene MP:0010225 abnormal quadriceps morphology IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0010227 decreased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15252120 734344 Itga7 integrin alpha 7 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16003770 734344 Itga7 integrin alpha 7 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22798625 734344 Itga7 integrin alpha 7 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9354797 734344 Itga7 integrin alpha 7 gene MP:0011904 abnormal Schwann cell physiology IAGP N RGD:5509061 20141003 MGI PMID:24227711 734344 Itga7 integrin alpha 7 gene MP:0020452 abnormal axon radial sorting IAGP N RGD:5509061 20170914 MGI PMID:24227711 734344 Itga7 integrin alpha 7 gene MP:0031318 enhanced skeletal muscle regeneration IAGP N RGD:5509061 20211125 MGI PMID:22798625 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16644867 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:12145326 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16644867 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12145326 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:16644867 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0001261 obese IAGP N RGD:5509061 20160929 MGI PMID:27534441 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12145326 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220602 MGI PMID:35245347 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20181227 MGI 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:16644867 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0001665 chronic diarrhea IAGP N RGD:5509061 20141003 MGI PMID:12145326 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20220602 MGI PMID:35245347 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16644867 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20220602 MGI PMID:35245347 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0002083 premature death IAGP N RGD:5509061 20220602 MGI PMID:35245347 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20220602 MGI PMID:35245347 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:12145326 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20181227 MGI 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12145326 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20181227 MGI 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20220602 MGI PMID:35245347 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:17050541 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:17490633 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:16644867 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:16644867 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:16644867 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005036 diarrhea IAGP N RGD:5509061 20160929 MGI PMID:27534441 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:12145326 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005128 decreased adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:12145326 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005128 decreased adrenocorticotropin level IAGP N RGD:5509061 20220602 MGI PMID:35245347 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20220602 MGI PMID:35245347 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:16644867 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12145326 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20160929 MGI PMID:27534441 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20160929 MGI PMID:27534441 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:16644867 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20220602 MGI PMID:35245347 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20220602 MGI PMID:35245347 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17490633 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16644867 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0008200 decreased follicular dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0008244 abnormal peritoneal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17490633 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22396549 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20181227 MGI 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12145326 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20220602 MGI PMID:35245347 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17490633 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12145326 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0011984 decreased enteroendocrine cell number IAGP N RGD:5509061 20220602 MGI PMID:35245347 734346 Pcsk1 proprotein convertase subtilisin/kexin type 1 gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20211021 MGI 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000627 abnormal mammary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:22777348 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000635 pituitary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000635 pituitary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000636 enlarged pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:16260494 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:19147535 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22777348 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22777348 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002208 abnormal germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002209 decreased germ cell number IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002348 abnormal lymph node medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002364 abnormal thymus size IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:16260494 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16260494 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19147535 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0006423 dilated rete testis IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0008117 abnormal Langerhans cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0008130 abnormal pituitary intermediate lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0008371 pituitary intermediate lobe hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9744866 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0009592 increased Leydig cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16260494 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22777348 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:17409423 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0010321 increased parathyroid gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0010384 increased renal carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0010829 increased bronchioalveolar stem cell number IAGP N RGD:5509061 20141003 MGI PMID:17409423 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17409423 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22777348 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0013602 abnormal Leydig cell differentiation IAGP N RGD:5509061 20150319 MGI PMID:11287627 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:10880462 734347 Cdkn2c cyclin dependent kinase inhibitor 2C gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:9744866 734349 Pip4k2a phosphatidylinositol-5-phosphate 4-kinase, type II, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24209622 734349 Pip4k2a phosphatidylinositol-5-phosphate 4-kinase, type II, alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24209622 734349 Pip4k2a phosphatidylinositol-5-phosphate 4-kinase, type II, alpha gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24209622 734349 Pip4k2a phosphatidylinositol-5-phosphate 4-kinase, type II, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24209622 734349 Pip4k2a phosphatidylinositol-5-phosphate 4-kinase, type II, alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24209622 734349 Pip4k2a phosphatidylinositol-5-phosphate 4-kinase, type II, alpha gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24209622 734353 Semg1 semenogelin 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20230601 MGI 734353 Semg1 semenogelin 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20150108 MGI PMID:24591616 734353 Semg1 semenogelin 1 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20150108 MGI PMID:24591616 734353 Semg1 semenogelin 1 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20150108 MGI PMID:24591616 734353 Semg1 semenogelin 1 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20150108 MGI PMID:24591616 734353 Semg1 semenogelin 1 gene MP:0005575 increased pulmonary ventilation IEA N RGD:5509061 20230601 MGI 734353 Semg1 semenogelin 1 gene MP:0013288 premature acrosome reaction IAGP N RGD:5509061 20150108 MGI PMID:24591616 734353 Semg1 semenogelin 1 gene MP:0030983 failure of copulatory plug deposition IAGP N RGD:5509061 20200102 MGI PMID:24591616 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210128 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0001293 anophthalmia IEA N RGD:5509061 20210128 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210128 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15385539 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0002188 small heart IEA N RGD:5509061 20210826 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210826 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20220811 MGI 734355 Gp2 glycoprotein 2 zymogen granule membrane gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000071 axial skeleton hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000088 short mandible IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000091 short premaxilla IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20221103 MGI 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000274 enlarged heart IEA N RGD:5509061 20221103 MGI 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:10080191 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20221103 MGI 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10080191 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0001649 abnormal mandibular symphysis morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10080191 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12471016 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10080191 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20221215 MGI 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0002639 micrognathia IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:10080192 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0003359 hypaxial muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0003586 dilated ureter IAGP N RGD:5509061 20141003 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:12932447 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0004017 duplex kidney IAGP N RGD:5509061 20141003 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0004454 absent pterygoid process IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0004592 small mandible IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:10080191 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22406547 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:12471016 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0005162 carpoptosis IAGP N RGD:5509061 20141003 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:10080191 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0008384 absent nasal capsule IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0008544 impaired olfaction IAGP N RGD:5509061 20141003 MGI PMID:10080191 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20161027 MGI PMID:10080191 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0009021 absent estrus IAGP N RGD:5509061 20141003 MGI PMID:10080191 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0009576 oral atresia IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0009709 hydrometra IEA N RGD:5509061 20221103 MGI 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20230323 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0009891 abnormal palate bone morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0009905 absent tongue IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20160407 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12471016 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16738228 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10080191 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20221103 MGI 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0011493 double ureter IAGP N RGD:5509061 20141003 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0011767 ureterocele IAGP N RGD:5509061 20141003 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0012538 persistent hyaloid artery IAGP N RGD:5509061 20141003 MGI PMID:19273906 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230323 MGI PMID:23863482 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0030013 enhanced central nervous system regeneration IAGP N RGD:5509061 20170713 MGI PMID:12932447 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0030013 enhanced central nervous system regeneration IAGP N RGD:5509061 20170713 MGI PMID:22406547 734358 Ptprs protein tyrosine phosphatase receptor type S gene MP:0031444 glossoptosis IAGP N RGD:5509061 20230323 MGI PMID:23863482 734359 Apba3 amyloid beta precursor protein binding family A member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17167098 734359 Apba3 amyloid beta precursor protein binding family A member 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17167098 734359 Apba3 amyloid beta precursor protein binding family A member 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:21778228 734359 Apba3 amyloid beta precursor protein binding family A member 3 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17167098 734359 Apba3 amyloid beta precursor protein binding family A member 3 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:21778228 734359 Apba3 amyloid beta precursor protein binding family A member 3 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21778228 734359 Apba3 amyloid beta precursor protein binding family A member 3 gene MP:0008618 decreased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:21778228 734359 Apba3 amyloid beta precursor protein binding family A member 3 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:21778228 734359 Apba3 amyloid beta precursor protein binding family A member 3 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:21778228 734359 Apba3 amyloid beta precursor protein binding family A member 3 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21778228 734359 Apba3 amyloid beta precursor protein binding family A member 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17167098 734365 Lrrn3 leucine rich repeat protein 3, neuronal gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20231207 MGI 734365 Lrrn3 leucine rich repeat protein 3, neuronal gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20141003 MGI 734365 Lrrn3 leucine rich repeat protein 3, neuronal gene MP:0005458 increased percent body fat/body weight IEA N RGD:5509061 20141003 MGI 734365 Lrrn3 leucine rich repeat protein 3, neuronal gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 734367 Ssrp1 structure specific recognition protein 1 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:12861016 734367 Ssrp1 structure specific recognition protein 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12861016 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0001147 small testis IAGP N RGD:5509061 20210506 MGI PMID:33206046 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20210506 MGI PMID:33206046 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20201231 MGI 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20210506 MGI PMID:33206046 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20210506 MGI PMID:33206046 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20210506 MGI PMID:33206046 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20181227 MGI 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20210506 MGI PMID:33206046 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20210506 MGI PMID:33206046 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20211021 MGI 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20210506 MGI PMID:33206046 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0004909 increased seminal vesicle weight IAGP N RGD:5509061 20210506 MGI PMID:33206046 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20210506 MGI PMID:33206046 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20211021 MGI 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0005573 increased pulmonary respiratory rate IEA N RGD:5509061 20211021 MGI 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20201022 MGI 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20210506 MGI PMID:33206046 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20210506 MGI PMID:33206046 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210506 MGI PMID:33206046 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 734369 Csnk1g2 casein kinase 1, gamma 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 734371 Usf2 upstream transcription factor 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:9520440 734371 Usf2 upstream transcription factor 2 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:9520440 734371 Usf2 upstream transcription factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9520440 734371 Usf2 upstream transcription factor 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:9520440 734371 Usf2 upstream transcription factor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9520440 734371 Usf2 upstream transcription factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9685363 734371 Usf2 upstream transcription factor 2 gene MP:0008237 abnormal ventral coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9520440 734371 Usf2 upstream transcription factor 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:9520440 734371 Usf2 upstream transcription factor 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:9520440 734371 Usf2 upstream transcription factor 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:9520440 734371 Usf2 upstream transcription factor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9520440 734371 Usf2 upstream transcription factor 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9520440 734371 Usf2 upstream transcription factor 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9520440 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000022 abnormal ear shape IAGP N RGD:5509061 20171026 MGI PMID:15492776 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:15492776 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:15492776 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17359964 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16556916 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000380 small hair follicles IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000414 alopecia IAGP N RGD:5509061 20200430 MGI PMID:20413717 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:20730911 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20200430 MGI PMID:20413717 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:11714671 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:16556916 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:11714671 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:11714671 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:11714671 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:15492776 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000568 ectopic digits IAGP N RGD:5509061 20141003 MGI PMID:11714671 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000579 abnormal nail morphology IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:16414041 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:16414041 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:15673568 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:15673568 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:15673568 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:18927151 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:18927151 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:8543149 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:8543149 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17359964 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8543149 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20200430 MGI PMID:20413717 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:12368913 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16414041 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002009 preneoplasia IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11857780 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8543149 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:11714671 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:20730911 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:15492776 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:16414041 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20730911 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11714671 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16037571 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16556916 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002789 male pseudohermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:12368913 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:16037571 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:15492776 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003221 abnormal cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16556916 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003299 gastric polyps IAGP N RGD:5509061 20200430 MGI PMID:20413717 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:15492776 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16556916 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:18927151 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003813 abnormal hair follicle dermal papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141003 MGI PMID:17359964 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003875 abnormal hair follicle regression IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:8543149 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0003892 abnormal gastric gland morphology IAGP N RGD:5509061 20200430 MGI PMID:20413717 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23736260 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0004421 enlarged parietal bone IAGP N RGD:5509061 20141003 MGI PMID:18927151 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:18927151 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:20730911 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15673568 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15492776 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18927151 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:18927151 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0006045 mitral valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:16037571 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0006198 enophthalmos IAGP N RGD:5509061 20141003 MGI PMID:20730911 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16414041 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15492776 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15673568 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0008275 failure of endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:18927151 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:15492776 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0010099 abnormal thoracic cage shape IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0010318 increased salivary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23736260 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0010512 absent PR interval IAGP N RGD:5509061 20141003 MGI PMID:16037571 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0010536 Ebstein's malformation of tricuspid valve IAGP N RGD:5509061 20141003 MGI PMID:16037571 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0010614 abnormal mitral valve cusp morphology IAGP N RGD:5509061 20141003 MGI PMID:16037571 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0010622 abnormal tricuspid valve cusp morphology IAGP N RGD:5509061 20141003 MGI PMID:16037571 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0010797 abnormal pyloric gastric gland morphology IAGP N RGD:5509061 20200430 MGI PMID:20413717 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0010811 decreased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:16414041 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16414041 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8543149 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16556916 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16887829 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17359964 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21068065 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20730911 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:8543149 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0011190 thick embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:8543149 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0011191 increased embryonic epiblast cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:8543149 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0011192 decreased embryonic epiblast cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8543149 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20730911 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0012110 increased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:23736260 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0012110 increased hair follicle number IAGP N RGD:5509061 20181129 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0013167 abnormal hindlimb bud morphology IAGP N RGD:5509061 20231130 MGI PMID:16556916 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0013169 small hindlimb buds IAGP N RGD:5509061 20231130 MGI PMID:16556916 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:17359964 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0014033 abnormal submucosal gland morphology IAGP N RGD:5509061 20200430 MGI PMID:20413717 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:23736260 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:18927151 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:18927151 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0020084 short ears IAGP N RGD:5509061 20171026 MGI PMID:15492776 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:15673568 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:15102710 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0030863 decreased joint mobility IAGP N RGD:5509061 20181101 MGI PMID:15492776 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0030866 abnormal synovial joint membrane morphology IAGP N RGD:5509061 20181101 MGI PMID:15492776 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0030886 decreased radius size IAGP N RGD:5509061 20181101 MGI PMID:15781876 734373 Bmpr1a bone morphogenetic protein receptor, type 1A gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:16037571 734375 Cdh13 cadherin 13 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:18316604 734375 Cdh13 cadherin 13 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 734375 Cdh13 cadherin 13 gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:18316604 734375 Cdh13 cadherin 13 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:18316604 734375 Cdh13 cadherin 13 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:18316604 734375 Cdh13 cadherin 13 gene MP:0003900 shortened QT interval IEA N RGD:5509061 20211021 MGI 734375 Cdh13 cadherin 13 gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:18316604 734375 Cdh13 cadherin 13 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 734375 Cdh13 cadherin 13 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:18316604 734375 Cdh13 cadherin 13 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18316604 734375 Cdh13 cadherin 13 gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:18316604 734379 Cacng5 calcium channel, voltage-dependent, gamma subunit 5 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210128 MGI 734381 Qdpr quinoid dihydropteridine reductase gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20150416 MGI PMID:25240194 734381 Qdpr quinoid dihydropteridine reductase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20150416 MGI PMID:25240194 734381 Qdpr quinoid dihydropteridine reductase gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:17151244 734381 Qdpr quinoid dihydropteridine reductase gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:17151244 734381 Qdpr quinoid dihydropteridine reductase gene MP:0005321 abnormal neopterin level IAGP N RGD:5509061 20150416 MGI PMID:25240194 734381 Qdpr quinoid dihydropteridine reductase gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17151244 734381 Qdpr quinoid dihydropteridine reductase gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20150416 MGI PMID:25240194 734381 Qdpr quinoid dihydropteridine reductase gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20150416 MGI PMID:25240194 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17034582 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17034582 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:11986227 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:17034582 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0002471 abnormal complement pathway IAGP N RGD:5509061 20141003 MGI PMID:9892684 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0002472 impaired complement alternative pathway IAGP N RGD:5509061 20141003 MGI PMID:9892684 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0002473 impaired complement classical pathway IAGP N RGD:5509061 20141003 MGI PMID:9892684 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:12003997 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:17034582 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0004823 increased susceptibility to experimental autoimmune myasthenia gravis IAGP N RGD:5509061 20141003 MGI PMID:12417565 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0004823 increased susceptibility to experimental autoimmune myasthenia gravis IAGP N RGD:5509061 20141003 MGI PMID:17034582 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:17383432 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12003997 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:18524992 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17034582 734384 Cd55 CD55 molecule, decay accelerating factor for complement gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:17034582 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000018 small ears IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000111 cleft palate IEA N RGD:5509061 20150827 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20150827 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141225 MGI PMID:23454479 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000477 abnormal intestine morphology IEA N RGD:5509061 20150827 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:19577771 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:19577771 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:19577771 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:19577771 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:22377357 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000561 adactyly IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000564 syndactyly IEA N RGD:5509061 20150827 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20230831 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:19577771 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:23095888 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:19577771 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:19577771 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19285468 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19285468 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20150101 MGI PMID:23454479 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20170622 MGI PMID:25043182 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:12142021 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0001178 pulmonary hypoplasia IEA N RGD:5509061 20150827 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19577771 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20170622 MGI PMID:25043182 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20170622 MGI PMID:25043182 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20170622 MGI PMID:25043182 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20150827 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20170622 MGI PMID:25043182 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0001935 decreased litter size IAGP N RGD:5509061 20170622 MGI PMID:25043182 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:12142021 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:19285468 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20150827 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20150827 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141225 MGI PMID:23454479 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:12142021 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0002632 vestigial tail IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20150827 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0002639 micrognathia IEA N RGD:5509061 20150827 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20141003 MGI PMID:22216013 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:24091014 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0003130 anal atresia IAGP N RGD:5509061 20141003 MGI PMID:19577771 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141225 MGI PMID:23454479 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0003380 abnormal intestine regeneration IAGP N RGD:5509061 20141003 MGI PMID:22956684 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141225 MGI PMID:23454479 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23095888 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20180503 MGI PMID:26526197 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20170622 MGI PMID:25043182 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0004550 short trachea IAGP N RGD:5509061 20141003 MGI PMID:12142021 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0004551 decreased tracheal cartilage ring number IAGP N RGD:5509061 20141003 MGI PMID:12142021 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0004653 absent caudal vertebrae IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:12142021 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0004733 abnormal thoracic cavity morphology IEA N RGD:5509061 20150827 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:22956684 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0005034 abnormal anus morphology IAGP N RGD:5509061 20141003 MGI PMID:19577771 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0005170 cleft upper lip IEA N RGD:5509061 20150827 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:24091014 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:22216013 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20150101 MGI PMID:23454479 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0008999 absent anus IAGP N RGD:5509061 20141003 MGI PMID:19577771 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0009204 absent external male genitalia IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0009211 absent external female genitalia IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0009284 abnormal sympathetic neuron innervation pattern IAGP N RGD:5509061 20141225 MGI PMID:23454479 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0009352 impaired spacing of implantation sites IAGP N RGD:5509061 20170622 MGI PMID:25043182 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0009353 twin decidual capsule IAGP N RGD:5509061 20170622 MGI PMID:25043182 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0009509 absent rectum IAGP N RGD:5509061 20141003 MGI PMID:19577771 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0009663 abnormal uterine-embryonic axis IAGP N RGD:5509061 20170622 MGI PMID:25043182 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20170622 MGI PMID:25043182 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0009705 abnormal midgut morphology IAGP N RGD:5509061 20141003 MGI PMID:24091014 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0010039 abnormal trophoblast giant cell proliferation IAGP N RGD:5509061 20170622 MGI PMID:25043182 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20150827 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0010446 heart left ventricle hypoplasia IEA N RGD:5509061 20150827 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0010460 pulmonary artery hypoplasia IEA N RGD:5509061 20150827 MGI 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12142021 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141225 MGI PMID:23454479 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19285468 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23095888 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20180503 MGI PMID:26526197 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20170622 MGI PMID:25043182 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0011772 genital tubercle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19577771 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0012182 abnormal presomitic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10021340 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160304 MGI PMID:19577771 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0014291 decreased autopod size IAGP N RGD:5509061 20230824 MGI PMID:22377357 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0030564 thick myocardium compact layer IAGP N RGD:5509061 20180524 MGI PMID:26526197 734385 Wnt5a wingless-type MMTV integration site family, member 5A gene MP:0030935 increased primordial germ cell apoptosis IAGP N RGD:5509061 20190411 MGI PMID:22216013 734387 Sdc2 syndecan 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 734387 Sdc2 syndecan 2 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20181227 MGI 734387 Sdc2 syndecan 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20160421 MGI 734387 Sdc2 syndecan 2 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20191107 MGI PMID:30952866 734387 Sdc2 syndecan 2 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20191107 MGI PMID:30952866 734387 Sdc2 syndecan 2 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20191107 MGI PMID:30952866 734387 Sdc2 syndecan 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20191107 MGI PMID:30952866 734387 Sdc2 syndecan 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20191107 MGI PMID:30952866 734387 Sdc2 syndecan 2 gene MP:0010068 decreased red blood cell distribution width IEA N RGD:5509061 20181227 MGI 734387 Sdc2 syndecan 2 gene MP:0010463 aorta stenosis IEA N RGD:5509061 20220811 MGI 734387 Sdc2 syndecan 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20181227 MGI 734387 Sdc2 syndecan 2 gene MP:0012201 decreased endothelial cell proliferation IAGP N RGD:5509061 20191107 MGI PMID:30952866 734387 Sdc2 syndecan 2 gene MP:0020316 decreased vascular endothelial cell proliferation IAGP N RGD:5509061 20191107 MGI PMID:30952866 734392 Mkln1 muskelin 1, intracellular mediator containing kelch motifs gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:21482357 734392 Mkln1 muskelin 1, intracellular mediator containing kelch motifs gene MP:0003245 abnormal GABAergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:21482357 734392 Mkln1 muskelin 1, intracellular mediator containing kelch motifs gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:21482357 734395 Zfp423 zinc finger protein 423 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12955145 734395 Zfp423 zinc finger protein 423 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17151198 734395 Zfp423 zinc finger protein 423 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:17151198 734395 Zfp423 zinc finger protein 423 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:17151198 734395 Zfp423 zinc finger protein 423 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17521568 734395 Zfp423 zinc finger protein 423 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:17151198 734395 Zfp423 zinc finger protein 423 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:17151198 734395 Zfp423 zinc finger protein 423 gene MP:0000829 dilated fourth ventricle IAGP N RGD:5509061 20141003 MGI PMID:17151198 734395 Zfp423 zinc finger protein 423 gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17151198 734395 Zfp423 zinc finger protein 423 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17521568 734395 Zfp423 zinc finger protein 423 gene MP:0000850 absent cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17151198 734395 Zfp423 zinc finger protein 423 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0000856 abnormal cerebellar plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0000865 absent cerebellum vermis IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17151198 734395 Zfp423 zinc finger protein 423 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17151198 734395 Zfp423 zinc finger protein 423 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17521568 734395 Zfp423 zinc finger protein 423 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20231207 MGI 734395 Zfp423 zinc finger protein 423 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12955145 734395 Zfp423 zinc finger protein 423 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17151198 734395 Zfp423 zinc finger protein 423 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17521568 734395 Zfp423 zinc finger protein 423 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20220519 MGI 734395 Zfp423 zinc finger protein 423 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17151198 734395 Zfp423 zinc finger protein 423 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12904583 734395 Zfp423 zinc finger protein 423 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:17151198 734395 Zfp423 zinc finger protein 423 gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:17521568 734395 Zfp423 zinc finger protein 423 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:17521568 734395 Zfp423 zinc finger protein 423 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 734395 Zfp423 zinc finger protein 423 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17151198 734395 Zfp423 zinc finger protein 423 gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17521568 734395 Zfp423 zinc finger protein 423 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17521568 734395 Zfp423 zinc finger protein 423 gene MP:0008221 abnormal hippocampal commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0008534 enlarged fourth ventricle IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17521568 734395 Zfp423 zinc finger protein 423 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0009804 abnormal brain interventricular foramen morphology IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0009965 abnormal cerebellum lateral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0009968 abnormal cerebellar granule cell precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12955145 734395 Zfp423 zinc finger protein 423 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17521568 734395 Zfp423 zinc finger protein 423 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17521568 734395 Zfp423 zinc finger protein 423 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17524391 734395 Zfp423 zinc finger protein 423 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 734395 Zfp423 zinc finger protein 423 gene MP:0012263 decreased hindbrain size IAGP N RGD:5509061 20141003 MGI PMID:16943432 734395 Zfp423 zinc finger protein 423 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:17524391 734397 Kcnh7 potassium voltage-gated channel, subfamily H (eag-related), member 7 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20221215 MGI 734399 Aatf apoptosis antagonizing transcription factor gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11071758 734399 Aatf apoptosis antagonizing transcription factor gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 734399 Aatf apoptosis antagonizing transcription factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11071758 734399 Aatf apoptosis antagonizing transcription factor gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20240926 MGI 734399 Aatf apoptosis antagonizing transcription factor gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:11071758 734399 Aatf apoptosis antagonizing transcription factor gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:11071758 734399 Aatf apoptosis antagonizing transcription factor gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240919 MGI 734399 Aatf apoptosis antagonizing transcription factor gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:11071758 734399 Aatf apoptosis antagonizing transcription factor gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11071758 734399 Aatf apoptosis antagonizing transcription factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 734399 Aatf apoptosis antagonizing transcription factor gene MP:0012111 failure of morula compaction IAGP N RGD:5509061 20141003 MGI PMID:11071758 734399 Aatf apoptosis antagonizing transcription factor gene MP:0012129 failure of blastocyst formation IAGP N RGD:5509061 20141003 MGI PMID:11071758 734399 Aatf apoptosis antagonizing transcription factor gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 734399 Aatf apoptosis antagonizing transcription factor gene MP:0014238 abnormal ribosome morphology IAGP N RGD:5509061 20230615 MGI PMID:11071758 734399 Aatf apoptosis antagonizing transcription factor gene MP:0014239 abnormal intracellular organelle morphology IAGP N RGD:5509061 20230615 MGI PMID:11071758 734401 Atp5f1a ATP synthase F1 subunit alpha gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 734401 Atp5f1a ATP synthase F1 subunit alpha gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11779834 734401 Atp5f1a ATP synthase F1 subunit alpha gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23870131 734402 Folr1 folate receptor alpha gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210805 MGI 734402 Folr1 folate receptor alpha gene MP:0000274 enlarged heart IEA N RGD:5509061 20210805 MGI 734402 Folr1 folate receptor alpha gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:15705887 734402 Folr1 folate receptor alpha gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:10508523 734402 Folr1 folate receptor alpha gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:10508523 734402 Folr1 folate receptor alpha gene MP:0001147 small testis IEA N RGD:5509061 20210805 MGI 734402 Folr1 folate receptor alpha gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:10508523 734402 Folr1 folate receptor alpha gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:10508523 734402 Folr1 folate receptor alpha gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210805 MGI 734402 Folr1 folate receptor alpha gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 734402 Folr1 folate receptor alpha gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:10508523 734402 Folr1 folate receptor alpha gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10508523 734402 Folr1 folate receptor alpha gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15705887 734402 Folr1 folate receptor alpha gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 734402 Folr1 folate receptor alpha gene MP:0006294 absent optic vesicle IAGP N RGD:5509061 20141003 MGI PMID:10508523 734402 Folr1 folate receptor alpha gene MP:0006342 absent first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:10508523 734402 Folr1 folate receptor alpha gene MP:0008725 increased heart atrium size IEA N RGD:5509061 20210805 MGI 734402 Folr1 folate receptor alpha gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15705887 734402 Folr1 folate receptor alpha gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10508523 734402 Folr1 folate receptor alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210805 MGI 734402 Folr1 folate receptor alpha gene MP:0011172 abnormal otic pit morphology IAGP N RGD:5509061 20141003 MGI PMID:10508523 734402 Folr1 folate receptor alpha gene MP:0011230 abnormal folic acid level IAGP N RGD:5509061 20141003 MGI PMID:15705887 734402 Folr1 folate receptor alpha gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:10508523 734402 Folr1 folate receptor alpha gene MP:0012335 increased circulating homocysteine level IAGP N RGD:5509061 20180920 MGI PMID:10508523 734402 Folr1 folate receptor alpha gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:10508523 734402 Folr1 folate receptor alpha gene MP:0012708 delayed rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:10508523 734402 Folr1 folate receptor alpha gene MP:0013183 absent trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:10508523 734402 Folr1 folate receptor alpha gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20220519 MGI 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:12915471 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12915471 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:12915471 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:12915471 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:12915471 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:12915471 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0005360 urolithiasis IAGP N RGD:5509061 20141003 MGI PMID:12915471 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0009645 crystalluria IAGP N RGD:5509061 20141003 MGI PMID:12915471 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:12915471 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:12915471 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0011799 increased urinary bladder weight IAGP N RGD:5509061 20141003 MGI PMID:12915471 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0020400 cystinuria IAGP N RGD:5509061 20161208 MGI PMID:12915471 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0020401 argininuria IAGP N RGD:5509061 20161208 MGI PMID:12915471 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0020402 ornithinuria IAGP N RGD:5509061 20161208 MGI PMID:12915471 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0020403 lysinuria IAGP N RGD:5509061 20161208 MGI PMID:12915471 734404 Slc7a9 solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene MP:0030617 hyperglutaminuria IAGP N RGD:5509061 20180906 MGI PMID:12915471 734406 Ank progressive ankylosis gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17186460 734406 Ank progressive ankylosis gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:17186460 734406 Ank progressive ankylosis gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:10894769 734406 Ank progressive ankylosis gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:1659102 734406 Ank progressive ankylosis gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17186460 734406 Ank progressive ankylosis gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16869722 734406 Ank progressive ankylosis gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10894769 734406 Ank progressive ankylosis gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16869722 734406 Ank progressive ankylosis gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:16869722 734406 Ank progressive ankylosis gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:10894769 734406 Ank progressive ankylosis gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:16869722 734406 Ank progressive ankylosis gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:17186460 734406 Ank progressive ankylosis gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:10894769 734406 Ank progressive ankylosis gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:16869722 734406 Ank progressive ankylosis gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0003198 calcified tendon IAGP N RGD:5509061 20181108 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0003200 calcified joint IAGP N RGD:5509061 20141003 MGI PMID:10894769 734406 Ank progressive ankylosis gene MP:0003200 calcified joint IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0003740 fusion of middle ear ossicles IAGP N RGD:5509061 20141003 MGI PMID:17186460 734406 Ank progressive ankylosis gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0003930 abnormal tooth hard tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:16869722 734406 Ank progressive ankylosis gene MP:0003933 abnormal cementum morphology IAGP N RGD:5509061 20141003 MGI PMID:16869722 734406 Ank progressive ankylosis gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:1659102 734406 Ank progressive ankylosis gene MP:0004685 calcified intervertebral disk IAGP N RGD:5509061 20141003 MGI PMID:1659102 734406 Ank progressive ankylosis gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:12817751 734406 Ank progressive ankylosis gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0005504 abnormal ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:16869722 734406 Ank progressive ankylosis gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0009005 abnormal sesamoid bone of gastrocnemius morphology IAGP N RGD:5509061 20141003 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0010522 calcified aorta IAGP N RGD:5509061 20141003 MGI PMID:15625282 734406 Ank progressive ankylosis gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:17186460 734406 Ank progressive ankylosis gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:17186460 734406 Ank progressive ankylosis gene MP:0010941 abnormal foramen magnum morphology IAGP N RGD:5509061 20141003 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0030094 foramen magnum stenosis IAGP N RGD:5509061 20170928 MGI PMID:17186460 734406 Ank progressive ankylosis gene MP:0030110 incudomalleolar fusion IAGP N RGD:5509061 20171005 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0030160 abnormal auditory bulla morphology IAGP N RGD:5509061 20171005 MGI PMID:17186460 734406 Ank progressive ankylosis gene MP:0030222 hyperostosis IAGP N RGD:5509061 20171019 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0030223 mandibular hyperostosis IAGP N RGD:5509061 20171019 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0030278 thick neurocranium IAGP N RGD:5509061 20171102 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0030310 abnormal cranial foramen morphology IAGP N RGD:5509061 20171207 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0030319 abnormal temporal bone petrous part morphology IAGP N RGD:5509061 20171109 MGI PMID:17186460 734406 Ank progressive ankylosis gene MP:0030382 absent paranasal sinus IAGP N RGD:5509061 20171207 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0030417 craniofacial hyperostosis IAGP N RGD:5509061 20171207 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0030791 club-shaped femur IAGP N RGD:5509061 20181011 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0030841 abnormal transverse acetabular ligament morphology IAGP N RGD:5509061 20181025 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0030863 decreased joint mobility IAGP N RGD:5509061 20181101 MGI PMID:10894769 734406 Ank progressive ankylosis gene MP:0030863 decreased joint mobility IAGP N RGD:5509061 20181101 MGI PMID:16869722 734406 Ank progressive ankylosis gene MP:0030863 decreased joint mobility IAGP N RGD:5509061 20181101 MGI PMID:19257826 734406 Ank progressive ankylosis gene MP:0030863 decreased joint mobility IAGP N RGD:5509061 20181101 MGI PMID:7276519 734406 Ank progressive ankylosis gene MP:0030865 abnormal synovial joint cavity morphology IAGP N RGD:5509061 20181108 MGI PMID:7276519 734408 Ppp6c protein phosphatase 6, catalytic subunit gene MP:0001219 thick epidermis IAGP N RGD:5509061 20160623 MGI PMID:25486434 734408 Ppp6c protein phosphatase 6, catalytic subunit gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20160623 MGI PMID:25486434 734408 Ppp6c protein phosphatase 6, catalytic subunit gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210128 MGI 734408 Ppp6c protein phosphatase 6, catalytic subunit gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20210826 MGI 734408 Ppp6c protein phosphatase 6, catalytic subunit gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20160623 MGI PMID:25486434 734408 Ppp6c protein phosphatase 6, catalytic subunit gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 734408 Ppp6c protein phosphatase 6, catalytic subunit gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 734408 Ppp6c protein phosphatase 6, catalytic subunit gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20160623 MGI PMID:25486434 734408 Ppp6c protein phosphatase 6, catalytic subunit gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 734408 Ppp6c protein phosphatase 6, catalytic subunit gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 734408 Ppp6c protein phosphatase 6, catalytic subunit gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20160623 MGI PMID:25486434 734408 Ppp6c protein phosphatase 6, catalytic subunit gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160623 MGI PMID:25486434 734408 Ppp6c protein phosphatase 6, catalytic subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 734408 Ppp6c protein phosphatase 6, catalytic subunit gene MP:0012572 increased susceptibility to chemically induced skin inflammation IAGP N RGD:5509061 20160623 MGI PMID:25486434 734408 Ppp6c protein phosphatase 6, catalytic subunit gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20160421 MGI 734411 Cadps Ca2+-dependent secretion activator gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:24174665 734411 Cadps Ca2+-dependent secretion activator gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:24174665 734411 Cadps Ca2+-dependent secretion activator gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20141003 MGI PMID:15820695 734411 Cadps Ca2+-dependent secretion activator gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20141003 MGI PMID:18495893 734411 Cadps Ca2+-dependent secretion activator gene MP:0001739 abnormal adrenal gland secretion IAGP N RGD:5509061 20190228 MGI PMID:25437547 734411 Cadps Ca2+-dependent secretion activator gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:15820695 734411 Cadps Ca2+-dependent secretion activator gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18177725 734411 Cadps Ca2+-dependent secretion activator gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:18022372 734411 Cadps Ca2+-dependent secretion activator gene MP:0002710 increased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:18177725 734411 Cadps Ca2+-dependent secretion activator gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18022372 734411 Cadps Ca2+-dependent secretion activator gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:18177725 734411 Cadps Ca2+-dependent secretion activator gene MP:0002909 abnormal adrenal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:15820695 734411 Cadps Ca2+-dependent secretion activator gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:18177725 734411 Cadps Ca2+-dependent secretion activator gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:18177725 734411 Cadps Ca2+-dependent secretion activator gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18177725 734411 Cadps Ca2+-dependent secretion activator gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:18177725 734411 Cadps Ca2+-dependent secretion activator gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18022372 734411 Cadps Ca2+-dependent secretion activator gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:24174665 734411 Cadps Ca2+-dependent secretion activator gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:24174665 734411 Cadps Ca2+-dependent secretion activator gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18022372 734411 Cadps Ca2+-dependent secretion activator gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21040848 734411 Cadps Ca2+-dependent secretion activator gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18177725 734411 Cadps Ca2+-dependent secretion activator gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18177725 734411 Cadps Ca2+-dependent secretion activator gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20190228 MGI PMID:25437547 734411 Cadps Ca2+-dependent secretion activator gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:24174665 734411 Cadps Ca2+-dependent secretion activator gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:24174665 734411 Cadps Ca2+-dependent secretion activator gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15820695 734411 Cadps Ca2+-dependent secretion activator gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18177725 734411 Cadps Ca2+-dependent secretion activator gene MP:0011267 abnormal excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:18022372 734411 Cadps Ca2+-dependent secretion activator gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:24174665 734411 Cadps Ca2+-dependent secretion activator gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:18022372 734411 Cadps Ca2+-dependent secretion activator gene MP:0014372 decreased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:18022372 734411 Cadps Ca2+-dependent secretion activator gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240328 MGI PMID:18022372 734411 Cadps Ca2+-dependent secretion activator gene MP:0030955 abnormal Golgi trans cisterna morphology IAGP N RGD:5509061 20190725 MGI PMID:24174665 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0000603 pale liver IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200402 MGI 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0002833 increased heart weight IEA N RGD:5509061 20201022 MGI 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0003926 decreased cellular glucose uptake IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20200402 MGI 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0009303 decreased renal fat pad weight IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0012634 decreased phospholipase A2 level IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0013245 abnormal lipid metabolism IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20170420 MGI PMID:19136964 734412 Plaat3 phospholipase A and acyltransferase 3 gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:19136964 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:16362077 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0000168 abnormal bone marrow development IAGP N RGD:5509061 20141003 MGI PMID:16362077 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:24469635 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:24469635 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0000884 delaminated Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:24469635 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16362077 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:16362077 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:16362077 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:24469635 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16362077 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:16362077 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:16362077 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:16362077 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:16362077 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16362077 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:24469635 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16362077 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:16362077 734417 Khdrbs1 KH domain containing, RNA binding, signal transduction associated 1 gene MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20220922 MGI PMID:16362077 734420 Apoa4 apolipoprotein A-IV gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9323588 734420 Apoa4 apolipoprotein A-IV gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:21356380 734420 Apoa4 apolipoprotein A-IV gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21356380 734420 Apoa4 apolipoprotein A-IV gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9323588 734420 Apoa4 apolipoprotein A-IV gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9323588 734420 Apoa4 apolipoprotein A-IV gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:21356380 734420 Apoa4 apolipoprotein A-IV gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:21356380 734420 Apoa4 apolipoprotein A-IV gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9323588 734420 Apoa4 apolipoprotein A-IV gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9323588 734420 Apoa4 apolipoprotein A-IV gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9323588 734420 Apoa4 apolipoprotein A-IV gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:21356380 734420 Apoa4 apolipoprotein A-IV gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:15254593 734420 Apoa4 apolipoprotein A-IV gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:9323588 734421 Fev FEV transcription factor, ETS family member gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20818386 734421 Fev FEV transcription factor, ETS family member gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:12546819 734421 Fev FEV transcription factor, ETS family member gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12546819 734421 Fev FEV transcription factor, ETS family member gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20818386 734421 Fev FEV transcription factor, ETS family member gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12546819 734421 Fev FEV transcription factor, ETS family member gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:20818386 734421 Fev FEV transcription factor, ETS family member gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20818386 734421 Fev FEV transcription factor, ETS family member gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:20818386 734421 Fev FEV transcription factor, ETS family member gene MP:0003877 abnormal serotonergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20818386 734421 Fev FEV transcription factor, ETS family member gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:20818386 734421 Fev FEV transcription factor, ETS family member gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:20818386 734421 Fev FEV transcription factor, ETS family member gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:12546819 734421 Fev FEV transcription factor, ETS family member gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:20818386 734421 Fev FEV transcription factor, ETS family member gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12546819 734422 Aadac arylacetamide deacetylase gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210520 MGI 734422 Aadac arylacetamide deacetylase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 734422 Aadac arylacetamide deacetylase gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210520 MGI 734422 Aadac arylacetamide deacetylase gene MP:0000706 small thymus IEA N RGD:5509061 20210520 MGI 734422 Aadac arylacetamide deacetylase gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 734422 Aadac arylacetamide deacetylase gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 734422 Aadac arylacetamide deacetylase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 734422 Aadac arylacetamide deacetylase gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 734422 Aadac arylacetamide deacetylase gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:18701681 734426 Psmc1 protease (prosome, macropain) 26S subunit, ATPase 1 gene MP:0012508 forebrain atrophy IAGP N RGD:5509061 20141003 MGI PMID:18701681 734429 Kif2c kinesin family member 2C gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20220825 MGI PMID:35138249 734429 Kif2c kinesin family member 2C gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 734429 Kif2c kinesin family member 2C gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20220825 MGI PMID:35138249 734429 Kif2c kinesin family member 2C gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20220825 MGI PMID:35138249 734429 Kif2c kinesin family member 2C gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20220825 MGI PMID:35138249 734429 Kif2c kinesin family member 2C gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20220825 MGI PMID:35138249 734429 Kif2c kinesin family member 2C gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20220825 MGI PMID:35138249 734429 Kif2c kinesin family member 2C gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20220825 MGI PMID:35138249 734429 Kif2c kinesin family member 2C gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 734429 Kif2c kinesin family member 2C gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20181227 MGI 734429 Kif2c kinesin family member 2C gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20220825 MGI PMID:35138249 734429 Kif2c kinesin family member 2C gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20220825 MGI PMID:35138249 734429 Kif2c kinesin family member 2C gene MP:0020422 decreased freezing behavior IAGP N RGD:5509061 20220825 MGI PMID:35138249 734429 Kif2c kinesin family member 2C gene MP:0020507 increased dendritic spine density IAGP N RGD:5509061 20220825 MGI PMID:35138249 734429 Kif2c kinesin family member 2C gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20220825 MGI PMID:35138249 734429 Kif2c kinesin family member 2C gene MP:0020512 abnormal dendritic mushroom spine morphology IAGP N RGD:5509061 20220825 MGI PMID:35138249 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0000129 ameloblast degeneration IAGP N RGD:5509061 20141003 MGI PMID:15265007 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:18395094 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:19023427 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:21659655 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0000314 schistocytosis IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:18039655 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18039655 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:18059474 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20230601 MGI 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10535991 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23238296 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15208274 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:17602956 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19023427 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23238296 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:23238296 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9558405 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12968018 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:15265007 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23238296 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18395094 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:15208274 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18039655 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23238296 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:15265007 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:15208274 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15060151 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15208274 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:19023427 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20161110 MGI PMID:27070823 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:15265007 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230601 MGI 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12646173 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23238296 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20141003 MGI PMID:17525273 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18039655 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18395094 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002944 increased lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20230601 MGI 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20230601 MGI 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:17602956 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003103 liver degeneration IAGP N RGD:5509061 20141003 MGI PMID:18039655 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:9558405 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:17525273 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:18059474 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20220519 MGI PMID:26247513 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003619 abnormal urine color IAGP N RGD:5509061 20141003 MGI PMID:23238296 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:19410644 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003668 abnormal periodontal ligament morphology IAGP N RGD:5509061 20161110 MGI PMID:27070823 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:12968018 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:17525273 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:18059474 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:19023427 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:19410644 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20161110 MGI PMID:27070823 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:17525273 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18039655 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18395094 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12968018 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18059474 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:11248092 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0004821 increased susceptibility to experimental autoimmune uveoretinitis IAGP N RGD:5509061 20141003 MGI PMID:19410644 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0004882 enlarged lung IAGP N RGD:5509061 20141003 MGI PMID:10535991 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17602956 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:17602956 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:18395094 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:21659655 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20220519 MGI PMID:26247513 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23238296 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19023427 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:18059474 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:12101242 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20230601 MGI 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19023427 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23238296 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20230601 MGI 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:15208274 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15265007 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20240523 MGI 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12968018 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18039655 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15208274 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:17602956 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:18039655 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:12968018 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:18039655 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:17178849 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:18395094 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21659655 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18395094 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:12101242 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:12101242 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:21659655 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008737 abnormal spleen physiology IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:12646173 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:15265007 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11248092 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15208274 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18395094 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10535991 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:12646173 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20220519 MGI PMID:26247513 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23238296 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0009322 increased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23238296 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20220519 MGI PMID:26247513 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:10535991 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18395094 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0010096 abnormal incisor color IAGP N RGD:5509061 20141003 MGI PMID:15265007 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0010177 acanthocytosis IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0010178 increased number of Howell-Jolly bodies IAGP N RGD:5509061 20141003 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:23238296 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11248092 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18039655 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12646173 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12968018 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:26247513 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:26247513 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20141003 MGI PMID:23238296 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:11576348 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011603 decreased glutathione peroxidase activity IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011625 cystolithiasis IAGP N RGD:5509061 20181025 MGI PMID:28165480 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:23238296 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0011971 increased circulating lactate dehydrogenase level IEA N RGD:5509061 20240523 MGI 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0012604 decreased glutathione level IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0012604 decreased glutathione level IAGP N RGD:5509061 20220519 MGI PMID:26247513 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0012652 decreased catalase level IAGP N RGD:5509061 20161110 MGI PMID:27070823 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0013129 abnormal tooth color IAGP N RGD:5509061 20220106 MGI PMID:15210949 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:12968018 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220519 MGI PMID:20692336 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0030466 alveolar process atrophy IAGP N RGD:5509061 20171221 MGI PMID:27070823 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:18395094 734432 Nfe2l2 nuclear factor, erythroid derived 2, like 2 gene MP:0031324 delayed liver regeneration IAGP N RGD:5509061 20220106 MGI PMID:18059474 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15888484 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15888484 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20151119 MGI PMID:22716256 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0002838 decreased susceptibility to dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:11526197 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0002838 decreased susceptibility to dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:12115029 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0002839 increased susceptibility to dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:11526197 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0002839 increased susceptibility to dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:12115029 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0002839 increased susceptibility to dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:16705021 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0002839 increased susceptibility to dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:8643601 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0003195 calcinosis IAGP N RGD:5509061 20141003 MGI PMID:16135817 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0003195 calcinosis IAGP N RGD:5509061 20151119 MGI PMID:22716256 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0003195 calcinosis IAGP N RGD:5509061 20181122 MGI PMID:28592560 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0003196 calcified skin IAGP N RGD:5509061 20141003 MGI PMID:15888484 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0003196 calcified skin IAGP N RGD:5509061 20141003 MGI PMID:16135817 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0003196 calcified skin IAGP N RGD:5509061 20181122 MGI PMID:28592560 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:16135817 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:15888484 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:15888484 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0006133 calcified artery IAGP N RGD:5509061 20141003 MGI PMID:15888484 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0006133 calcified artery IAGP N RGD:5509061 20141003 MGI PMID:16135817 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0006188 calcified retina IAGP N RGD:5509061 20141003 MGI PMID:16135817 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16135817 734434 Abcc6 ATP-binding cassette, sub-family C member 6 gene MP:0030533 abnormal snout skin morphology IAGP N RGD:5509061 20181122 MGI PMID:28592560 734438 Skap2 src family associated phosphoprotein 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20150212 MGI PMID:24815314 734438 Skap2 src family associated phosphoprotein 2 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16135797 734438 Skap2 src family associated phosphoprotein 2 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20150212 MGI PMID:24815314 734438 Skap2 src family associated phosphoprotein 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19369640 734438 Skap2 src family associated phosphoprotein 2 gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:19369640 734438 Skap2 src family associated phosphoprotein 2 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:16135797 734438 Skap2 src family associated phosphoprotein 2 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16135797 734438 Skap2 src family associated phosphoprotein 2 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:16135797 734438 Skap2 src family associated phosphoprotein 2 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16135797 734438 Skap2 src family associated phosphoprotein 2 gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20150212 MGI PMID:24815314 734438 Skap2 src family associated phosphoprotein 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20151112 MGI PMID:24846415 734438 Skap2 src family associated phosphoprotein 2 gene MP:0012319 fast extinction of fear memory IAGP N RGD:5509061 20150212 MGI PMID:24815314 734440 Upb1 ureidopropionase, beta gene MP:0001258 decreased body length IEA N RGD:5509061 20201022 MGI 734440 Upb1 ureidopropionase, beta gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 734440 Upb1 ureidopropionase, beta gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 734442 Nup155 nucleoporin 155 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 734442 Nup155 nucleoporin 155 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 734442 Nup155 nucleoporin 155 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 734442 Nup155 nucleoporin 155 gene MP:0001728 failure of embryo implantation IEA N RGD:5509061 20240926 MGI 734442 Nup155 nucleoporin 155 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 734442 Nup155 nucleoporin 155 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:19070573 734442 Nup155 nucleoporin 155 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240926 MGI 734442 Nup155 nucleoporin 155 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:19070573 734442 Nup155 nucleoporin 155 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 734442 Nup155 nucleoporin 155 gene MP:0008543 atrial fibrillation IAGP N RGD:5509061 20141003 MGI PMID:19070573 734442 Nup155 nucleoporin 155 gene MP:0010504 abnormal RR interval IAGP N RGD:5509061 20141003 MGI PMID:19070573 734442 Nup155 nucleoporin 155 gene MP:0010510 absent P wave IAGP N RGD:5509061 20141003 MGI PMID:19070573 734442 Nup155 nucleoporin 155 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19070573 734442 Nup155 nucleoporin 155 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 734442 Nup155 nucleoporin 155 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 734442 Nup155 nucleoporin 155 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240926 MGI 734446 Cited1 Cbp/p300-interacting transactivator with Glu/Asp-rich carboxy-terminal domain 1 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:16278680 734446 Cited1 Cbp/p300-interacting transactivator with Glu/Asp-rich carboxy-terminal domain 1 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:16278680 734446 Cited1 Cbp/p300-interacting transactivator with Glu/Asp-rich carboxy-terminal domain 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:14673158 734446 Cited1 Cbp/p300-interacting transactivator with Glu/Asp-rich carboxy-terminal domain 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:14673158 734446 Cited1 Cbp/p300-interacting transactivator with Glu/Asp-rich carboxy-terminal domain 1 gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:14673158 734446 Cited1 Cbp/p300-interacting transactivator with Glu/Asp-rich carboxy-terminal domain 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:14673158 734446 Cited1 Cbp/p300-interacting transactivator with Glu/Asp-rich carboxy-terminal domain 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:14673158 734446 Cited1 Cbp/p300-interacting transactivator with Glu/Asp-rich carboxy-terminal domain 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:14673158 734446 Cited1 Cbp/p300-interacting transactivator with Glu/Asp-rich carboxy-terminal domain 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:14673158 734446 Cited1 Cbp/p300-interacting transactivator with Glu/Asp-rich carboxy-terminal domain 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14673158 734446 Cited1 Cbp/p300-interacting transactivator with Glu/Asp-rich carboxy-terminal domain 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17615577 734446 Cited1 Cbp/p300-interacting transactivator with Glu/Asp-rich carboxy-terminal domain 1 gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20141003 MGI PMID:14673158 734446 Cited1 Cbp/p300-interacting transactivator with Glu/Asp-rich carboxy-terminal domain 1 gene MP:0011527 disorganized placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:14673158 734446 Cited1 Cbp/p300-interacting transactivator with Glu/Asp-rich carboxy-terminal domain 1 gene MP:0012098 increased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:14673158 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:10942411 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20221215 MGI 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:18178860 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:7568173 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:7697542 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:8839836 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:7697542 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:8839836 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:18178860 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18178860 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:7697542 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:7568173 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:7697542 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:8839836 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18178860 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20141003 MGI PMID:7697542 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20141003 MGI PMID:8839836 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0004924 abnormal behavior IEA N RGD:5509061 20221215 MGI 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20221215 MGI 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:7568173 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:7697542 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8839836 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18178860 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18178860 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18178860 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:18178860 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:18178860 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:18178860 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:18178860 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:18178860 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18178860 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18178860 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0010998 pulmonary alveolar proteinosis IAGP N RGD:5509061 20141003 MGI PMID:7568173 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20221215 MGI 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20221215 MGI 734448 Csf2rb colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20221215 MGI 734450 Rheb Ras homolog enriched in brain gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:21321084 734450 Rheb Ras homolog enriched in brain gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:21321084 734450 Rheb Ras homolog enriched in brain gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:21238928 734450 Rheb Ras homolog enriched in brain gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:21238928 734450 Rheb Ras homolog enriched in brain gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21321084 734450 Rheb Ras homolog enriched in brain gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21238928 734450 Rheb Ras homolog enriched in brain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21238928 734450 Rheb Ras homolog enriched in brain gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23426372 734450 Rheb Ras homolog enriched in brain gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:21238928 734450 Rheb Ras homolog enriched in brain gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20201022 MGI PMID:29961810 734450 Rheb Ras homolog enriched in brain gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20201022 MGI PMID:29961810 734450 Rheb Ras homolog enriched in brain gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:23426372 734450 Rheb Ras homolog enriched in brain gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:21238928 734450 Rheb Ras homolog enriched in brain gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23426372 734450 Rheb Ras homolog enriched in brain gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21321084 734450 Rheb Ras homolog enriched in brain gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:23426372 734450 Rheb Ras homolog enriched in brain gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:21321084 734450 Rheb Ras homolog enriched in brain gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21321084 734450 Rheb Ras homolog enriched in brain gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:23426372 734450 Rheb Ras homolog enriched in brain gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20201022 MGI PMID:29961810 734450 Rheb Ras homolog enriched in brain gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20201022 MGI PMID:29961810 734450 Rheb Ras homolog enriched in brain gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:23426372 734450 Rheb Ras homolog enriched in brain gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:21321084 734450 Rheb Ras homolog enriched in brain gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:23426372 734450 Rheb Ras homolog enriched in brain gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:21238928 734450 Rheb Ras homolog enriched in brain gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:21238928 734450 Rheb Ras homolog enriched in brain gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:23426372 734450 Rheb Ras homolog enriched in brain gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23426372 734450 Rheb Ras homolog enriched in brain gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23426372 734450 Rheb Ras homolog enriched in brain gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21238928 734450 Rheb Ras homolog enriched in brain gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21321084 734450 Rheb Ras homolog enriched in brain gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21321084 734450 Rheb Ras homolog enriched in brain gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:21321084 734450 Rheb Ras homolog enriched in brain gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:21321084 734450 Rheb Ras homolog enriched in brain gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:21321084 734454 Lonp1 lon peptidase 1, mitochondrial gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20231207 MGI 734454 Lonp1 lon peptidase 1, mitochondrial gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 734454 Lonp1 lon peptidase 1, mitochondrial gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160218 MGI PMID:25017063 734454 Lonp1 lon peptidase 1, mitochondrial gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20160218 MGI PMID:25017063 734454 Lonp1 lon peptidase 1, mitochondrial gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160218 MGI PMID:25017063 734454 Lonp1 lon peptidase 1, mitochondrial gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20211021 MGI 734454 Lonp1 lon peptidase 1, mitochondrial gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20160218 MGI PMID:25017063 734454 Lonp1 lon peptidase 1, mitochondrial gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20160218 MGI PMID:25017063 734454 Lonp1 lon peptidase 1, mitochondrial gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 734454 Lonp1 lon peptidase 1, mitochondrial gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 734454 Lonp1 lon peptidase 1, mitochondrial gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20160218 MGI PMID:25017063 734454 Lonp1 lon peptidase 1, mitochondrial gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20160218 MGI PMID:25017063 734455 Lat linker for activation of T cells gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20180830 MGI PMID:29902238 734455 Lat linker for activation of T cells gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:23793062 734455 Lat linker for activation of T cells gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:17081783 734455 Lat linker for activation of T cells gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17081783 734455 Lat linker for activation of T cells gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19682930 734455 Lat linker for activation of T cells gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17081783 734455 Lat linker for activation of T cells gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:15238603 734455 Lat linker for activation of T cells gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:10204488 734455 Lat linker for activation of T cells gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:11457888 734455 Lat linker for activation of T cells gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:12871507 734455 Lat linker for activation of T cells gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:19380807 734455 Lat linker for activation of T cells gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10204488 734455 Lat linker for activation of T cells gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:12871507 734455 Lat linker for activation of T cells gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19380807 734455 Lat linker for activation of T cells gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180830 MGI PMID:29902238 734455 Lat linker for activation of T cells gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20200514 MGI 734455 Lat linker for activation of T cells gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:23793062 734455 Lat linker for activation of T cells gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15238603 734455 Lat linker for activation of T cells gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18209052 734455 Lat linker for activation of T cells gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10204488 734455 Lat linker for activation of T cells gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12871507 734455 Lat linker for activation of T cells gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19380761 734455 Lat linker for activation of T cells gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19380807 734455 Lat linker for activation of T cells gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19701892 734455 Lat linker for activation of T cells gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:19682930 734455 Lat linker for activation of T cells gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20180830 MGI PMID:29902238 734455 Lat linker for activation of T cells gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20180830 MGI PMID:29902238 734455 Lat linker for activation of T cells gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15238603 734455 Lat linker for activation of T cells gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:15238603 734455 Lat linker for activation of T cells gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20180830 MGI PMID:29902238 734455 Lat linker for activation of T cells gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20180830 MGI PMID:29902238 734455 Lat linker for activation of T cells gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11457888 734455 Lat linker for activation of T cells gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12871507 734455 Lat linker for activation of T cells gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19380807 734455 Lat linker for activation of T cells gene MP:0002221 abnormal lymph organ size IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0002346 abnormal lymph node secondary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0002358 abnormal spleen periarteriolar lymphoid sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23793062 734455 Lat linker for activation of T cells gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0002407 abnormal double-negative T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16878135 734455 Lat linker for activation of T cells gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15477348 734455 Lat linker for activation of T cells gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15477350 734455 Lat linker for activation of T cells gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17081783 734455 Lat linker for activation of T cells gene MP:0002434 abnormal T-helper 2 cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0002435 abnormal effector T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19380807 734455 Lat linker for activation of T cells gene MP:0002439 abnormal plasma cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18539897 734455 Lat linker for activation of T cells gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19380807 734455 Lat linker for activation of T cells gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:23793062 734455 Lat linker for activation of T cells gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:19682930 734455 Lat linker for activation of T cells gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19701892 734455 Lat linker for activation of T cells gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20201022 MGI 734455 Lat linker for activation of T cells gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0003334 pancreas fibrosis IAGP N RGD:5509061 20180830 MGI PMID:29902238 734455 Lat linker for activation of T cells gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20180830 MGI PMID:29902238 734455 Lat linker for activation of T cells gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:17081783 734455 Lat linker for activation of T cells gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0004797 increased anti-erythrocyte antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0004827 increased susceptibility to autoimmune hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0004917 abnormal T cell selection IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18209052 734455 Lat linker for activation of T cells gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20180830 MGI PMID:29902238 734455 Lat linker for activation of T cells gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18209052 734455 Lat linker for activation of T cells gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19380807 734455 Lat linker for activation of T cells gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10204488 734455 Lat linker for activation of T cells gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11457888 734455 Lat linker for activation of T cells gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12871507 734455 Lat linker for activation of T cells gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:17579183 734455 Lat linker for activation of T cells gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:10204488 734455 Lat linker for activation of T cells gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:12871507 734455 Lat linker for activation of T cells gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:19701892 734455 Lat linker for activation of T cells gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19380807 734455 Lat linker for activation of T cells gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19380761 734455 Lat linker for activation of T cells gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18209052 734455 Lat linker for activation of T cells gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 734455 Lat linker for activation of T cells gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:18209052 734455 Lat linker for activation of T cells gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:19682930 734455 Lat linker for activation of T cells gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10204488 734455 Lat linker for activation of T cells gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:19380807 734455 Lat linker for activation of T cells gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:15238603 734455 Lat linker for activation of T cells gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19682930 734455 Lat linker for activation of T cells gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19380807 734455 Lat linker for activation of T cells gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19380807 734455 Lat linker for activation of T cells gene MP:0008081 abnormal single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20141003 MGI PMID:23793062 734455 Lat linker for activation of T cells gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0008344 abnormal mature gamma-delta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19380807 734455 Lat linker for activation of T cells gene MP:0008353 increased mature gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0008355 absent mature gamma-delta T cells IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0008356 abnormal gamma-delta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0008356 abnormal gamma-delta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12065840 734455 Lat linker for activation of T cells gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:19682930 734455 Lat linker for activation of T cells gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20180830 MGI PMID:29902238 734455 Lat linker for activation of T cells gene MP:0008522 abnormal lymph node germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:16887989 734455 Lat linker for activation of T cells gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19682930 734455 Lat linker for activation of T cells gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:12065839 734455 Lat linker for activation of T cells gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15153499 734455 Lat linker for activation of T cells gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19682930 734455 Lat linker for activation of T cells gene MP:0008757 abnormal T cell receptor gamma chain V-J recombination IAGP N RGD:5509061 20141003 MGI PMID:19701892 734455 Lat linker for activation of T cells gene MP:0008759 abnormal T cell receptor delta chain V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:19701892 734455 Lat linker for activation of T cells gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0008827 abnormal thymus cell ratio IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:12970761 734455 Lat linker for activation of T cells gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20141003 MGI PMID:17579183 734455 Lat linker for activation of T cells gene MP:0009548 abnormal platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:12871507 734455 Lat linker for activation of T cells gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:17579183 734455 Lat linker for activation of T cells gene MP:0010140 phlebitis IAGP N RGD:5509061 20180830 MGI PMID:29902238 734455 Lat linker for activation of T cells gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:16887989 734457 Lgals3bp lectin, galactoside-binding, soluble, 3 binding protein gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:10077627 734457 Lgals3bp lectin, galactoside-binding, soluble, 3 binding protein gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:10077627 734457 Lgals3bp lectin, galactoside-binding, soluble, 3 binding protein gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:10077627 734457 Lgals3bp lectin, galactoside-binding, soluble, 3 binding protein gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:10077627 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16618416 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:16618416 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16618417 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:16618416 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:16618417 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16618416 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16618416 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16618416 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16618416 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:16618416 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:16618417 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16618416 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16618416 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0005285 decreased unsaturated fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16618416 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0005286 decreased saturated fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16618416 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:16618417 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16618417 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:16618417 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16618416 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:16618417 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16618417 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16618417 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16618417 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16618416 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16618416 734459 Slc27a5 solute carrier family 27 (fatty acid transporter), member 5 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:16618417 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20240125 MGI PMID:35064213 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21368763 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20240125 MGI PMID:35064213 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21368763 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20220407 MGI PMID:34625556 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:21368763 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0001192 scaly skin IAGP N RGD:5509061 20240125 MGI PMID:35064213 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0001212 skin lesions IAGP N RGD:5509061 20240125 MGI PMID:35064213 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240125 MGI PMID:35064213 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20201022 MGI 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22195746 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20160204 MGI 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0002220 large lymphoid organs IAGP N RGD:5509061 20141003 MGI PMID:21368763 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0003288 intestinal edema IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0003717 pallor IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0004155 decreased susceptibility to induced pancreatitis IAGP N RGD:5509061 20141003 MGI PMID:19524512 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:21368763 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0005036 diarrhea IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0008542 enlarged cervical lymph nodes IAGP N RGD:5509061 20170713 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0008891 decreased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21368763 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:19524512 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21368763 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0009631 enlarged axillary lymph nodes IAGP N RGD:5509061 20170713 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22195746 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210506 MGI PMID:33206046 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0011081 decreased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22327219 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20240125 MGI PMID:35064213 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20141003 MGI PMID:21368762 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20150219 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0013648 increased CD11b-high dendritic cell number IAGP N RGD:5509061 20240125 MGI PMID:35064213 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0014080 fused small intestinal villi IAGP N RGD:5509061 20160310 MGI PMID:24557836 734463 Ripk3 receptor-interacting serine-threonine kinase 3 gene MP:0014083 blunted small intestinal villi IAGP N RGD:5509061 20160310 MGI PMID:24557836 735242 Abi2 abl interactor 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:15572692 735242 Abi2 abl interactor 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15572692 735242 Abi2 abl interactor 2 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15572692 735242 Abi2 abl interactor 2 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:15572692 735242 Abi2 abl interactor 2 gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 735242 Abi2 abl interactor 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15572692 735242 Abi2 abl interactor 2 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:15572692 735242 Abi2 abl interactor 2 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20181227 MGI 735242 Abi2 abl interactor 2 gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20181227 MGI 735242 Abi2 abl interactor 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 735242 Abi2 abl interactor 2 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20181227 MGI 735242 Abi2 abl interactor 2 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15572692 735242 Abi2 abl interactor 2 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 735242 Abi2 abl interactor 2 gene MP:0002579 disorganized secondary lens fibers IAGP N RGD:5509061 20141003 MGI PMID:15572692 735242 Abi2 abl interactor 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 735242 Abi2 abl interactor 2 gene MP:0003236 abnormal lens capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:15572692 735242 Abi2 abl interactor 2 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16401422 735242 Abi2 abl interactor 2 gene MP:0005102 abnormal iris pigmentation IEA N RGD:5509061 20181227 MGI 735242 Abi2 abl interactor 2 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:15572692 735242 Abi2 abl interactor 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21173240 735242 Abi2 abl interactor 2 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:15572692 735242 Abi2 abl interactor 2 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:15572692 735242 Abi2 abl interactor 2 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:16401422 735242 Abi2 abl interactor 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210520 MGI 735242 Abi2 abl interactor 2 gene MP:0009252 absent urinary bladder IEA N RGD:5509061 20181227 MGI 735242 Abi2 abl interactor 2 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15572692 735242 Abi2 abl interactor 2 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15572692 735242 Abi2 abl interactor 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 735248 Cd69 CD69 antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:10733501 735248 Cd69 CD69 antigen gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:22474373 735248 Cd69 CD69 antigen gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10733501 735248 Cd69 CD69 antigen gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22474373 735248 Cd69 CD69 antigen gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:10733501 735248 Cd69 CD69 antigen gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10733501 735248 Cd69 CD69 antigen gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:12882836 735248 Cd69 CD69 antigen gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22474373 735248 Cd69 CD69 antigen gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22474373 735248 Cd69 CD69 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22474373 735248 Cd69 CD69 antigen gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10733501 735248 Cd69 CD69 antigen gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:10733501 735248 Cd69 CD69 antigen gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22474373 735248 Cd69 CD69 antigen gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22474373 735248 Cd69 CD69 antigen gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:12882836 735248 Cd69 CD69 antigen gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12882836 735252 Rbp4 retinol binding protein 4, plasma gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20180920 MGI PMID:29330472 735252 Rbp4 retinol binding protein 4, plasma gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:12663486 735252 Rbp4 retinol binding protein 4, plasma gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12663486 735252 Rbp4 retinol binding protein 4, plasma gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20180920 MGI PMID:29330472 735252 Rbp4 retinol binding protein 4, plasma gene MP:0000604 amyloidosis IAGP N RGD:5509061 20180920 MGI PMID:29330472 735252 Rbp4 retinol binding protein 4, plasma gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:16586441 735252 Rbp4 retinol binding protein 4, plasma gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:16586441 735252 Rbp4 retinol binding protein 4, plasma gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20210128 MGI 735252 Rbp4 retinol binding protein 4, plasma gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20150910 MGI PMID:24852372 735252 Rbp4 retinol binding protein 4, plasma gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200116 MGI PMID:26974396 735252 Rbp4 retinol binding protein 4, plasma gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:16586441 735252 Rbp4 retinol binding protein 4, plasma gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:10469643 735252 Rbp4 retinol binding protein 4, plasma gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20180920 MGI PMID:29330472 735252 Rbp4 retinol binding protein 4, plasma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16586441 735252 Rbp4 retinol binding protein 4, plasma gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20200116 MGI PMID:26974396 735252 Rbp4 retinol binding protein 4, plasma gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12663486 735252 Rbp4 retinol binding protein 4, plasma gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:16586441 735252 Rbp4 retinol binding protein 4, plasma gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12663486 735252 Rbp4 retinol binding protein 4, plasma gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20141003 MGI PMID:16586441 735252 Rbp4 retinol binding protein 4, plasma gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20200116 MGI PMID:26974396 735252 Rbp4 retinol binding protein 4, plasma gene MP:0005400 abnormal vitamin level IAGP N RGD:5509061 20141003 MGI PMID:16586441 735252 Rbp4 retinol binding protein 4, plasma gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10469643 735252 Rbp4 retinol binding protein 4, plasma gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 735252 Rbp4 retinol binding protein 4, plasma gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 735252 Rbp4 retinol binding protein 4, plasma gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:16586441 735252 Rbp4 retinol binding protein 4, plasma gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20200116 MGI PMID:26974396 735252 Rbp4 retinol binding protein 4, plasma gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:26974396 735252 Rbp4 retinol binding protein 4, plasma gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200116 MGI PMID:26974396 735252 Rbp4 retinol binding protein 4, plasma gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200116 MGI PMID:26974396 735252 Rbp4 retinol binding protein 4, plasma gene MP:0011234 abnormal retinol level IAGP N RGD:5509061 20141003 MGI PMID:10469643 735252 Rbp4 retinol binding protein 4, plasma gene MP:0011234 abnormal retinol level IAGP N RGD:5509061 20141003 MGI PMID:16586441 735252 Rbp4 retinol binding protein 4, plasma gene MP:0011234 abnormal retinol level IAGP N RGD:5509061 20200116 MGI PMID:26974396 735252 Rbp4 retinol binding protein 4, plasma gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200116 MGI PMID:26974396 735252 Rbp4 retinol binding protein 4, plasma gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:26974396 735252 Rbp4 retinol binding protein 4, plasma gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200116 MGI PMID:26974396 735252 Rbp4 retinol binding protein 4, plasma gene MP:0012147 increased a-wave implicit time IAGP N RGD:5509061 20200116 MGI PMID:26974396 735252 Rbp4 retinol binding protein 4, plasma gene MP:0012150 increased b-wave implicit time IAGP N RGD:5509061 20200116 MGI PMID:26974396 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11533705 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:11972032 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:11533705 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:16403066 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20200521 MGI PMID:30371314 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11972032 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16403066 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16403066 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11533705 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17083109 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:21824921 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170817 MGI PMID:21824921 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0002833 increased heart weight IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11972032 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:11533705 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:11972032 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:15809371 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:16403066 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:17145985 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:22287583 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20160324 MGI PMID:24895455 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20200521 MGI PMID:30371314 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15809371 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:11533705 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:15809371 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:17145985 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:22287583 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:11972032 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:15809371 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:21824921 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:22287583 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20160324 MGI PMID:24895455 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20200521 MGI PMID:30371314 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003899 abnormal QT interval IAGP N RGD:5509061 20200521 MGI PMID:30371314 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0003900 shortened QT interval IAGP N RGD:5509061 20141003 MGI PMID:21566215 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:11972032 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:11972032 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:15809371 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:21824921 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20160324 MGI PMID:24895455 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0004116 abnormal atrioventricular bundle conduction IAGP N RGD:5509061 20160324 MGI PMID:24895455 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:11972032 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:16403066 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:17145985 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:21566215 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:21824921 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20160324 MGI PMID:24895455 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:11972032 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21824921 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11972032 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11533705 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15809371 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17145985 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:21824921 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20200521 MGI PMID:30371314 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0005630 increased lung weight IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0006110 ventricular fibrillation IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0006141 abnormal atrioventricular node conduction IAGP N RGD:5509061 20141003 MGI PMID:22287583 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:17145985 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:21824921 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:22287583 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20200521 MGI PMID:30371314 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:21824921 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0008543 atrial fibrillation IAGP N RGD:5509061 20141003 MGI PMID:21824921 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:11972032 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:16403066 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:21097662 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:21824921 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20200521 MGI PMID:30371314 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16403066 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:15809371 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:17145985 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:21824921 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:22287583 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20160324 MGI PMID:24895455 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20200521 MGI PMID:30371314 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010393 shortened QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:21566215 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010505 abnormal T wave IAGP N RGD:5509061 20141003 MGI PMID:11533705 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:21824921 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20200521 MGI PMID:30371314 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010511 shortened PR interval IAGP N RGD:5509061 20141003 MGI PMID:21566215 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:21824921 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:22287583 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20200521 MGI PMID:30371314 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20141003 MGI PMID:22287583 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20200521 MGI PMID:30371314 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16403066 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16403066 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17145985 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11533705 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11972032 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20200521 MGI PMID:30144447 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0011953 prolonged PQ interval IAGP N RGD:5509061 20141003 MGI PMID:17145985 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:16403066 735253 Scn5a sodium channel, voltage-gated, type V, alpha gene MP:0020347 abnormal myocardial fiber sodium currents IAGP N RGD:5509061 20200521 MGI PMID:30144447 735255 Lyz2 lysozyme 2 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20151015 MGI PMID:19933310 735255 Lyz2 lysozyme 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20180426 MGI PMID:28287403 735255 Lyz2 lysozyme 2 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:21876000 735255 Lyz2 lysozyme 2 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20151015 MGI PMID:19933310 735255 Lyz2 lysozyme 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14769860 735255 Lyz2 lysozyme 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20053716 735255 Lyz2 lysozyme 2 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20180426 MGI PMID:28287403 735255 Lyz2 lysozyme 2 gene MP:0000172 abnormal bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20180830 MGI PMID:28771483 735255 Lyz2 lysozyme 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23204105 735255 Lyz2 lysozyme 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17476360 735255 Lyz2 lysozyme 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18278031 735255 Lyz2 lysozyme 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180301 MGI PMID:25016030 735255 Lyz2 lysozyme 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20457873 735255 Lyz2 lysozyme 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22201685 735255 Lyz2 lysozyme 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20180301 MGI PMID:25016030 735255 Lyz2 lysozyme 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12759446 735255 Lyz2 lysozyme 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12759446 735255 Lyz2 lysozyme 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17062731 735255 Lyz2 lysozyme 2 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23460613 735255 Lyz2 lysozyme 2 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17548584 735255 Lyz2 lysozyme 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20141003 MGI PMID:22322302 735255 Lyz2 lysozyme 2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19398754 735255 Lyz2 lysozyme 2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:21876000 735255 Lyz2 lysozyme 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:17062731 735255 Lyz2 lysozyme 2 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:17404282 735255 Lyz2 lysozyme 2 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:12727921 735255 Lyz2 lysozyme 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17404282 735255 Lyz2 lysozyme 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17476360 735255 Lyz2 lysozyme 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20240530 MGI PMID:38478630 735255 Lyz2 lysozyme 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:24122813 735255 Lyz2 lysozyme 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:17476360 735255 Lyz2 lysozyme 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12874264 735255 Lyz2 lysozyme 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21364283 735255 Lyz2 lysozyme 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:24122813 735255 Lyz2 lysozyme 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180830 MGI PMID:28771483 735255 Lyz2 lysozyme 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:24122813 735255 Lyz2 lysozyme 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20190926 MGI PMID:31126966 735255 Lyz2 lysozyme 2 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0000717 abnormal lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:23460747 735255 Lyz2 lysozyme 2 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17404282 735255 Lyz2 lysozyme 2 gene MP:0001190 reddish skin IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20180830 MGI PMID:28771483 735255 Lyz2 lysozyme 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180830 MGI PMID:28771483 735255 Lyz2 lysozyme 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:12486099 735255 Lyz2 lysozyme 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15142530 735255 Lyz2 lysozyme 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17476360 735255 Lyz2 lysozyme 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23921126 735255 Lyz2 lysozyme 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17404282 735255 Lyz2 lysozyme 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23460747 735255 Lyz2 lysozyme 2 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20180830 MGI PMID:28771483 735255 Lyz2 lysozyme 2 gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:17404282 735255 Lyz2 lysozyme 2 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:20053716 735255 Lyz2 lysozyme 2 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20180830 MGI PMID:28771483 735255 Lyz2 lysozyme 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0001577 anemia IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:15664162 735255 Lyz2 lysozyme 2 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17476360 735255 Lyz2 lysozyme 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:15142530 735255 Lyz2 lysozyme 2 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:19913445 735255 Lyz2 lysozyme 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:17895374 735255 Lyz2 lysozyme 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:18566402 735255 Lyz2 lysozyme 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:20062524 735255 Lyz2 lysozyme 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:22624878 735255 Lyz2 lysozyme 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:24302768 735255 Lyz2 lysozyme 2 gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10944538 735255 Lyz2 lysozyme 2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17111348 735255 Lyz2 lysozyme 2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17275357 735255 Lyz2 lysozyme 2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20150625 MGI PMID:25698726 735255 Lyz2 lysozyme 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12411294 735255 Lyz2 lysozyme 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12628185 735255 Lyz2 lysozyme 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22348103 735255 Lyz2 lysozyme 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20210121 MGI PMID:32668247 735255 Lyz2 lysozyme 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20210617 MGI PMID:31883536 735255 Lyz2 lysozyme 2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20210708 MGI PMID:33513427 735255 Lyz2 lysozyme 2 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:15142530 735255 Lyz2 lysozyme 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:19286998 735255 Lyz2 lysozyme 2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20210610 MGI PMID:31826938 735255 Lyz2 lysozyme 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12628185 735255 Lyz2 lysozyme 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20150917 MGI PMID:24995976 735255 Lyz2 lysozyme 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23722907 735255 Lyz2 lysozyme 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:17404282 735255 Lyz2 lysozyme 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17476360 735255 Lyz2 lysozyme 2 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21364283 735255 Lyz2 lysozyme 2 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:24122813 735255 Lyz2 lysozyme 2 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17476360 735255 Lyz2 lysozyme 2 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22201685 735255 Lyz2 lysozyme 2 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17476360 735255 Lyz2 lysozyme 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15142530 735255 Lyz2 lysozyme 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17275357 735255 Lyz2 lysozyme 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17404282 735255 Lyz2 lysozyme 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18039655 735255 Lyz2 lysozyme 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20308544 735255 Lyz2 lysozyme 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21930766 735255 Lyz2 lysozyme 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23460747 735255 Lyz2 lysozyme 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24122813 735255 Lyz2 lysozyme 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:20053716 735255 Lyz2 lysozyme 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17476360 735255 Lyz2 lysozyme 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:22322302 735255 Lyz2 lysozyme 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20151015 MGI PMID:19933310 735255 Lyz2 lysozyme 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:17404282 735255 Lyz2 lysozyme 2 gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:17404282 735255 Lyz2 lysozyme 2 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22862945 735255 Lyz2 lysozyme 2 gene MP:0002410 decreased susceptibility to viral infection IAGP N RGD:5509061 20220929 MGI PMID:36028484 735255 Lyz2 lysozyme 2 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:19286998 735255 Lyz2 lysozyme 2 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21494554 735255 Lyz2 lysozyme 2 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:22573811 735255 Lyz2 lysozyme 2 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20180906 MGI PMID:28476751 735255 Lyz2 lysozyme 2 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20240222 MGI PMID:27936058 735255 Lyz2 lysozyme 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15664162 735255 Lyz2 lysozyme 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17275357 735255 Lyz2 lysozyme 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:19286998 735255 Lyz2 lysozyme 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:20226692 735255 Lyz2 lysozyme 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:24302768 735255 Lyz2 lysozyme 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20191003 MGI PMID:31189603 735255 Lyz2 lysozyme 2 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20457873 735255 Lyz2 lysozyme 2 gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0002415 abnormal neutrophil differentiation IAGP N RGD:5509061 20141003 MGI PMID:18278031 735255 Lyz2 lysozyme 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17111048 735255 Lyz2 lysozyme 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23204105 735255 Lyz2 lysozyme 2 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:22624878 735255 Lyz2 lysozyme 2 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20180322 MGI PMID:28348104 735255 Lyz2 lysozyme 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10944538 735255 Lyz2 lysozyme 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12628185 735255 Lyz2 lysozyme 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:12754505 735255 Lyz2 lysozyme 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15142530 735255 Lyz2 lysozyme 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16862162 735255 Lyz2 lysozyme 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17275357 735255 Lyz2 lysozyme 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17709479 735255 Lyz2 lysozyme 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:20062524 735255 Lyz2 lysozyme 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:22357629 735255 Lyz2 lysozyme 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:22624878 735255 Lyz2 lysozyme 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:24302768 735255 Lyz2 lysozyme 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20180322 MGI PMID:28348104 735255 Lyz2 lysozyme 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20191003 MGI PMID:31189603 735255 Lyz2 lysozyme 2 gene MP:0002454 abnormal macrophage antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:22624878 735255 Lyz2 lysozyme 2 gene MP:0002458 abnormal B cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16988010 735255 Lyz2 lysozyme 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17062731 735255 Lyz2 lysozyme 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17202315 735255 Lyz2 lysozyme 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:18278031 735255 Lyz2 lysozyme 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:19286998 735255 Lyz2 lysozyme 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:19797524 735255 Lyz2 lysozyme 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20180614 MGI PMID:24176643 735255 Lyz2 lysozyme 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20200806 MGI PMID:31285585 735255 Lyz2 lysozyme 2 gene MP:0002472 impaired complement alternative pathway IAGP N RGD:5509061 20141003 MGI PMID:20941861 735255 Lyz2 lysozyme 2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:15142530 735255 Lyz2 lysozyme 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20150917 MGI PMID:24995976 735255 Lyz2 lysozyme 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180830 MGI PMID:28771483 735255 Lyz2 lysozyme 2 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20220922 MGI PMID:34921782 735255 Lyz2 lysozyme 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:12727921 735255 Lyz2 lysozyme 2 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:17895374 735255 Lyz2 lysozyme 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20150917 MGI PMID:24995976 735255 Lyz2 lysozyme 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:20733032 735255 Lyz2 lysozyme 2 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0002936 joint swelling IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:22586041 735255 Lyz2 lysozyme 2 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20240530 MGI PMID:38478630 735255 Lyz2 lysozyme 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17111348 735255 Lyz2 lysozyme 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17275357 735255 Lyz2 lysozyme 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20191003 MGI PMID:31189603 735255 Lyz2 lysozyme 2 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20210121 MGI PMID:32668247 735255 Lyz2 lysozyme 2 gene MP:0003075 abnormal response to CNS ischemic injury IAGP N RGD:5509061 20141003 MGI PMID:19147818 735255 Lyz2 lysozyme 2 gene MP:0003075 abnormal response to CNS ischemic injury IAGP N RGD:5509061 20161103 MGI PMID:23637179 735255 Lyz2 lysozyme 2 gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20150917 MGI PMID:24995976 735255 Lyz2 lysozyme 2 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:23178822 735255 Lyz2 lysozyme 2 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15142530 735255 Lyz2 lysozyme 2 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:12628185 735255 Lyz2 lysozyme 2 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20941861 735255 Lyz2 lysozyme 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20308544 735255 Lyz2 lysozyme 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20200903 MGI PMID:32001710 735255 Lyz2 lysozyme 2 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15142530 735255 Lyz2 lysozyme 2 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:22322302 735255 Lyz2 lysozyme 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20180405 MGI PMID:24739962 735255 Lyz2 lysozyme 2 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19147818 735255 Lyz2 lysozyme 2 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:22322302 735255 Lyz2 lysozyme 2 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22201685 735255 Lyz2 lysozyme 2 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20112392 735255 Lyz2 lysozyme 2 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:17895374 735255 Lyz2 lysozyme 2 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20180426 MGI PMID:28287403 735255 Lyz2 lysozyme 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12628185 735255 Lyz2 lysozyme 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20231695 735255 Lyz2 lysozyme 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20180322 MGI PMID:28348104 735255 Lyz2 lysozyme 2 gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:19286998 735255 Lyz2 lysozyme 2 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:22577176 735255 Lyz2 lysozyme 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:24302768 735255 Lyz2 lysozyme 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20180322 MGI PMID:28348104 735255 Lyz2 lysozyme 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20200903 MGI PMID:32001710 735255 Lyz2 lysozyme 2 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20240222 MGI PMID:27936058 735255 Lyz2 lysozyme 2 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20180830 MGI PMID:28771483 735255 Lyz2 lysozyme 2 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20220922 MGI PMID:34921782 735255 Lyz2 lysozyme 2 gene MP:0004049 increased acute promyelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21930766 735255 Lyz2 lysozyme 2 gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20180614 MGI PMID:24176643 735255 Lyz2 lysozyme 2 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22201685 735255 Lyz2 lysozyme 2 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23090995 735255 Lyz2 lysozyme 2 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:17404282 735255 Lyz2 lysozyme 2 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:19398754 735255 Lyz2 lysozyme 2 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20180405 MGI PMID:24739962 735255 Lyz2 lysozyme 2 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23722907 735255 Lyz2 lysozyme 2 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:23204105 735255 Lyz2 lysozyme 2 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20150917 MGI PMID:24995976 735255 Lyz2 lysozyme 2 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20180531 MGI PMID:28533230 735255 Lyz2 lysozyme 2 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20240222 MGI PMID:27936058 735255 Lyz2 lysozyme 2 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:14769860 735255 Lyz2 lysozyme 2 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20151015 MGI PMID:19933310 735255 Lyz2 lysozyme 2 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:20053716 735255 Lyz2 lysozyme 2 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:21876000 735255 Lyz2 lysozyme 2 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20180426 MGI PMID:28287403 735255 Lyz2 lysozyme 2 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20151015 MGI PMID:19933310 735255 Lyz2 lysozyme 2 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:21876000 735255 Lyz2 lysozyme 2 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:21876000 735255 Lyz2 lysozyme 2 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17062731 735255 Lyz2 lysozyme 2 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20180531 MGI PMID:28533230 735255 Lyz2 lysozyme 2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20180301 MGI PMID:25016030 735255 Lyz2 lysozyme 2 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19398754 735255 Lyz2 lysozyme 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 735255 Lyz2 lysozyme 2 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17476360 735255 Lyz2 lysozyme 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:22577176 735255 Lyz2 lysozyme 2 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15142530 735255 Lyz2 lysozyme 2 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:18978793 735255 Lyz2 lysozyme 2 gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:22467660 735255 Lyz2 lysozyme 2 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15142530 735255 Lyz2 lysozyme 2 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:19941312 735255 Lyz2 lysozyme 2 gene MP:0005036 diarrhea IAGP N RGD:5509061 20210121 MGI PMID:32668247 735255 Lyz2 lysozyme 2 gene MP:0005040 abnormal MHC II cell surface expression on macrophages IAGP N RGD:5509061 20141003 MGI PMID:10621974 735255 Lyz2 lysozyme 2 gene MP:0005065 abnormal neutrophil morphology IAGP N RGD:5509061 20180614 MGI PMID:24176643 735255 Lyz2 lysozyme 2 gene MP:0005074 impaired granulocyte bactericidal activity IAGP N RGD:5509061 20141003 MGI PMID:19797524 735255 Lyz2 lysozyme 2 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:12759446 735255 Lyz2 lysozyme 2 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:17111048 735255 Lyz2 lysozyme 2 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22586041 735255 Lyz2 lysozyme 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:18423196 735255 Lyz2 lysozyme 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:21242513 735255 Lyz2 lysozyme 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22573811 735255 Lyz2 lysozyme 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0005238 increased brain size IAGP N RGD:5509061 20180830 MGI PMID:28771483 735255 Lyz2 lysozyme 2 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20150917 MGI PMID:24995976 735255 Lyz2 lysozyme 2 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22101429 735255 Lyz2 lysozyme 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20150917 MGI PMID:24995976 735255 Lyz2 lysozyme 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20220721 MGI PMID:30067966 735255 Lyz2 lysozyme 2 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20180830 MGI PMID:28771483 735255 Lyz2 lysozyme 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:12411294 735255 Lyz2 lysozyme 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20210617 MGI PMID:31883536 735255 Lyz2 lysozyme 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20220721 MGI PMID:30067966 735255 Lyz2 lysozyme 2 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17038633 735255 Lyz2 lysozyme 2 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:18988889 735255 Lyz2 lysozyme 2 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17038633 735255 Lyz2 lysozyme 2 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:22586041 735255 Lyz2 lysozyme 2 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23460747 735255 Lyz2 lysozyme 2 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20112392 735255 Lyz2 lysozyme 2 gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:15664162 735255 Lyz2 lysozyme 2 gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:20062524 735255 Lyz2 lysozyme 2 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:20516367 735255 Lyz2 lysozyme 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:12727921 735255 Lyz2 lysozyme 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:19398754 735255 Lyz2 lysozyme 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:22201685 735255 Lyz2 lysozyme 2 gene MP:0005426 tachypnea IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0005426 tachypnea IAGP N RGD:5509061 20141003 MGI PMID:23460747 735255 Lyz2 lysozyme 2 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0005535 abnormal body temperature IAGP N RGD:5509061 20141003 MGI PMID:17548584 735255 Lyz2 lysozyme 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20180614 MGI PMID:24176643 735255 Lyz2 lysozyme 2 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23460747 735255 Lyz2 lysozyme 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17079175 735255 Lyz2 lysozyme 2 gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20180531 MGI PMID:28533230 735255 Lyz2 lysozyme 2 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20220120 MGI PMID:33859201 735255 Lyz2 lysozyme 2 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:17476360 735255 Lyz2 lysozyme 2 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:20308544 735255 Lyz2 lysozyme 2 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20240530 MGI PMID:38478630 735255 Lyz2 lysozyme 2 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20240718 MGI PMID:33895792 735255 Lyz2 lysozyme 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20180830 MGI PMID:28771483 735255 Lyz2 lysozyme 2 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20150917 MGI PMID:24995976 735255 Lyz2 lysozyme 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18039655 735255 Lyz2 lysozyme 2 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:19147818 735255 Lyz2 lysozyme 2 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:19147818 735255 Lyz2 lysozyme 2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20457873 735255 Lyz2 lysozyme 2 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17476360 735255 Lyz2 lysozyme 2 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20308544 735255 Lyz2 lysozyme 2 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:19913445 735255 Lyz2 lysozyme 2 gene MP:0008050 decreased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19913445 735255 Lyz2 lysozyme 2 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19913445 735255 Lyz2 lysozyme 2 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0008070 absent T cells IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0008071 absent B cells IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0008073 abnormal CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12727921 735255 Lyz2 lysozyme 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19398754 735255 Lyz2 lysozyme 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 735255 Lyz2 lysozyme 2 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0008077 abnormal CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19398754 735255 Lyz2 lysozyme 2 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19913445 735255 Lyz2 lysozyme 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20141003 MGI PMID:15322156 735255 Lyz2 lysozyme 2 gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20141003 MGI PMID:22624878 735255 Lyz2 lysozyme 2 gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20180322 MGI PMID:28348104 735255 Lyz2 lysozyme 2 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:12727921 735255 Lyz2 lysozyme 2 gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 735255 Lyz2 lysozyme 2 gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:12874264 735255 Lyz2 lysozyme 2 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 735255 Lyz2 lysozyme 2 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20161103 MGI PMID:23637179 735255 Lyz2 lysozyme 2 gene MP:0008240 abnormal spleen marginal zone macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:12874264 735255 Lyz2 lysozyme 2 gene MP:0008244 abnormal peritoneal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:17404282 735255 Lyz2 lysozyme 2 gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:19286998 735255 Lyz2 lysozyme 2 gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20180531 MGI PMID:28533230 735255 Lyz2 lysozyme 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:14769860 735255 Lyz2 lysozyme 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:18548006 735255 Lyz2 lysozyme 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21876000 735255 Lyz2 lysozyme 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20151015 MGI PMID:19933310 735255 Lyz2 lysozyme 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20180426 MGI PMID:28287403 735255 Lyz2 lysozyme 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20220120 MGI PMID:33859201 735255 Lyz2 lysozyme 2 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:18039655 735255 Lyz2 lysozyme 2 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:18039655 735255 Lyz2 lysozyme 2 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20210617 MGI PMID:31883536 735255 Lyz2 lysozyme 2 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20210121 MGI PMID:32668247 735255 Lyz2 lysozyme 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:22201685 735255 Lyz2 lysozyme 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20191024 MGI PMID:31383741 735255 Lyz2 lysozyme 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20210610 MGI PMID:31826938 735255 Lyz2 lysozyme 2 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:23454745 735255 Lyz2 lysozyme 2 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20170518 MGI PMID:25732303 735255 Lyz2 lysozyme 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19398754 735255 Lyz2 lysozyme 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19941312 735255 Lyz2 lysozyme 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:21119595 735255 Lyz2 lysozyme 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22201685 735255 Lyz2 lysozyme 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22348103 735255 Lyz2 lysozyme 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22586041 735255 Lyz2 lysozyme 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:23460747 735255 Lyz2 lysozyme 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20180426 MGI PMID:28287403 735255 Lyz2 lysozyme 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20180906 MGI PMID:28476751 735255 Lyz2 lysozyme 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20200806 MGI PMID:31285585 735255 Lyz2 lysozyme 2 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20210610 MGI PMID:31826938 735255 Lyz2 lysozyme 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15664162 735255 Lyz2 lysozyme 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17709479 735255 Lyz2 lysozyme 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22467660 735255 Lyz2 lysozyme 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22573811 735255 Lyz2 lysozyme 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20191003 MGI PMID:31189603 735255 Lyz2 lysozyme 2 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20240530 MGI PMID:38478630 735255 Lyz2 lysozyme 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 735255 Lyz2 lysozyme 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21119595 735255 Lyz2 lysozyme 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22348103 735255 Lyz2 lysozyme 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23178822 735255 Lyz2 lysozyme 2 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20210617 MGI PMID:31883536 735255 Lyz2 lysozyme 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:12628185 735255 Lyz2 lysozyme 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17548584 735255 Lyz2 lysozyme 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:20062524 735255 Lyz2 lysozyme 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22573811 735255 Lyz2 lysozyme 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23090995 735255 Lyz2 lysozyme 2 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20150917 MGI PMID:24995976 735255 Lyz2 lysozyme 2 gene MP:0008564 increased interferon-beta secretion IAGP N RGD:5509061 20220929 MGI PMID:36028484 735255 Lyz2 lysozyme 2 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20141003 MGI PMID:19398754 735255 Lyz2 lysozyme 2 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20201210 MGI PMID:31320558 735255 Lyz2 lysozyme 2 gene MP:0008565 decreased interferon-beta secretion IAGP N RGD:5509061 20230105 MGI PMID:36217001 735255 Lyz2 lysozyme 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 735255 Lyz2 lysozyme 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19398754 735255 Lyz2 lysozyme 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20112392 735255 Lyz2 lysozyme 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 735255 Lyz2 lysozyme 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22393151 735255 Lyz2 lysozyme 2 gene MP:0008574 decreased circulating interferon-alpha level IAGP N RGD:5509061 20141003 MGI PMID:21494554 735255 Lyz2 lysozyme 2 gene MP:0008575 increased circulating interferon-beta level IAGP N RGD:5509061 20220929 MGI PMID:36028484 735255 Lyz2 lysozyme 2 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20141003 MGI PMID:21494554 735255 Lyz2 lysozyme 2 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20191003 MGI PMID:31189603 735255 Lyz2 lysozyme 2 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20201210 MGI PMID:31320558 735255 Lyz2 lysozyme 2 gene MP:0008576 decreased circulating interferon-beta level IAGP N RGD:5509061 20230105 MGI PMID:36217001 735255 Lyz2 lysozyme 2 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:19941312 735255 Lyz2 lysozyme 2 gene MP:0008577 increased circulating interferon-gamma level IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:21119595 735255 Lyz2 lysozyme 2 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:23241891 735255 Lyz2 lysozyme 2 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20200806 MGI PMID:31285585 735255 Lyz2 lysozyme 2 gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:22348103 735255 Lyz2 lysozyme 2 gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20180906 MGI PMID:28476751 735255 Lyz2 lysozyme 2 gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21119595 735255 Lyz2 lysozyme 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:22201685 735255 Lyz2 lysozyme 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20180906 MGI PMID:28476751 735255 Lyz2 lysozyme 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20200806 MGI PMID:31285585 735255 Lyz2 lysozyme 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20210610 MGI PMID:31826938 735255 Lyz2 lysozyme 2 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18423196 735255 Lyz2 lysozyme 2 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:22573811 735255 Lyz2 lysozyme 2 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20191003 MGI PMID:31189603 735255 Lyz2 lysozyme 2 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20230105 MGI PMID:36217001 735255 Lyz2 lysozyme 2 gene MP:0008599 increased circulating interleukin-2 level IAGP N RGD:5509061 20141003 MGI PMID:19941312 735255 Lyz2 lysozyme 2 gene MP:0008614 increased circulating interleukin-17 level IAGP N RGD:5509061 20141003 MGI PMID:19941312 735255 Lyz2 lysozyme 2 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:19941312 735255 Lyz2 lysozyme 2 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:22201685 735255 Lyz2 lysozyme 2 gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:24302768 735255 Lyz2 lysozyme 2 gene MP:0008638 increased circulating interleukin-1 alpha level IAGP N RGD:5509061 20141003 MGI PMID:19941312 735255 Lyz2 lysozyme 2 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:19941312 735255 Lyz2 lysozyme 2 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:22201685 735255 Lyz2 lysozyme 2 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:22348103 735255 Lyz2 lysozyme 2 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:24302768 735255 Lyz2 lysozyme 2 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20210121 MGI PMID:32668247 735255 Lyz2 lysozyme 2 gene MP:0008642 decreased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:22467660 735255 Lyz2 lysozyme 2 gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:17548584 735255 Lyz2 lysozyme 2 gene MP:0008655 decreased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:23090995 735255 Lyz2 lysozyme 2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:20112392 735255 Lyz2 lysozyme 2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:22348103 735255 Lyz2 lysozyme 2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:24302768 735255 Lyz2 lysozyme 2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20161103 MGI PMID:23637179 735255 Lyz2 lysozyme 2 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20210617 MGI PMID:31883536 735255 Lyz2 lysozyme 2 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:17548584 735255 Lyz2 lysozyme 2 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:23090995 735255 Lyz2 lysozyme 2 gene MP:0008658 decreased interleukin-1 beta secretion IAGP N RGD:5509061 20150917 MGI PMID:24995976 735255 Lyz2 lysozyme 2 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:22348103 735255 Lyz2 lysozyme 2 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:21119595 735255 Lyz2 lysozyme 2 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:22348103 735255 Lyz2 lysozyme 2 gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 735255 Lyz2 lysozyme 2 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:17548584 735255 Lyz2 lysozyme 2 gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 735255 Lyz2 lysozyme 2 gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20180531 MGI PMID:28533230 735255 Lyz2 lysozyme 2 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:20112392 735255 Lyz2 lysozyme 2 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:22862945 735255 Lyz2 lysozyme 2 gene MP:0008684 increased interleukin-18 secretion IAGP N RGD:5509061 20141003 MGI PMID:24302768 735255 Lyz2 lysozyme 2 gene MP:0008690 increased interleukin-23 secretion IAGP N RGD:5509061 20141003 MGI PMID:22862945 735255 Lyz2 lysozyme 2 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20180531 MGI PMID:28533230 735255 Lyz2 lysozyme 2 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:22393151 735255 Lyz2 lysozyme 2 gene MP:0008704 abnormal interleukin-6 secretion IAGP N RGD:5509061 20161103 MGI PMID:23637179 735255 Lyz2 lysozyme 2 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 735255 Lyz2 lysozyme 2 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:20112392 735255 Lyz2 lysozyme 2 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21119595 735255 Lyz2 lysozyme 2 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:22348103 735255 Lyz2 lysozyme 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17548584 735255 Lyz2 lysozyme 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:23090995 735255 Lyz2 lysozyme 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20150917 MGI PMID:24995976 735255 Lyz2 lysozyme 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20230105 MGI PMID:36217001 735255 Lyz2 lysozyme 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:19286998 735255 Lyz2 lysozyme 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:19941312 735255 Lyz2 lysozyme 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:23460747 735255 Lyz2 lysozyme 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20210610 MGI PMID:31826938 735255 Lyz2 lysozyme 2 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:12759446 735255 Lyz2 lysozyme 2 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:17062731 735255 Lyz2 lysozyme 2 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:19286998 735255 Lyz2 lysozyme 2 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:20231695 735255 Lyz2 lysozyme 2 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:23460613 735255 Lyz2 lysozyme 2 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12759446 735255 Lyz2 lysozyme 2 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20231695 735255 Lyz2 lysozyme 2 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:19941312 735255 Lyz2 lysozyme 2 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15664162 735255 Lyz2 lysozyme 2 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:20112392 735255 Lyz2 lysozyme 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12727921 735255 Lyz2 lysozyme 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12754507 735255 Lyz2 lysozyme 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:15664162 735255 Lyz2 lysozyme 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17548584 735255 Lyz2 lysozyme 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17709479 735255 Lyz2 lysozyme 2 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:21778228 735255 Lyz2 lysozyme 2 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:17111348 735255 Lyz2 lysozyme 2 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:21119595 735255 Lyz2 lysozyme 2 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:22201685 735255 Lyz2 lysozyme 2 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:22348103 735255 Lyz2 lysozyme 2 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:24302768 735255 Lyz2 lysozyme 2 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20201210 MGI PMID:31320558 735255 Lyz2 lysozyme 2 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20240718 MGI PMID:33895792 735255 Lyz2 lysozyme 2 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20240718 MGI PMID:33895792 735255 Lyz2 lysozyme 2 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0008838 decreased transforming growth factor beta level IAGP N RGD:5509061 20180906 MGI PMID:28476751 735255 Lyz2 lysozyme 2 gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:24302768 735255 Lyz2 lysozyme 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20210617 MGI PMID:31883536 735255 Lyz2 lysozyme 2 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20457873 735255 Lyz2 lysozyme 2 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20150917 MGI PMID:24995976 735255 Lyz2 lysozyme 2 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20180830 MGI PMID:28771483 735255 Lyz2 lysozyme 2 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20180830 MGI PMID:28771483 735255 Lyz2 lysozyme 2 gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22201685 735255 Lyz2 lysozyme 2 gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19398754 735255 Lyz2 lysozyme 2 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0009625 abnormal abdominal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:20724542 735255 Lyz2 lysozyme 2 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22763442 735255 Lyz2 lysozyme 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15664162 735255 Lyz2 lysozyme 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22348103 735255 Lyz2 lysozyme 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210121 MGI PMID:32668247 735255 Lyz2 lysozyme 2 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22573811 735255 Lyz2 lysozyme 2 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22201685 735255 Lyz2 lysozyme 2 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17548584 735255 Lyz2 lysozyme 2 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21778228 735255 Lyz2 lysozyme 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19286998 735255 Lyz2 lysozyme 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20191003 MGI PMID:31189603 735255 Lyz2 lysozyme 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20200806 MGI PMID:31285585 735255 Lyz2 lysozyme 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20210610 MGI PMID:31826938 735255 Lyz2 lysozyme 2 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19286998 735255 Lyz2 lysozyme 2 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19398754 735255 Lyz2 lysozyme 2 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22573811 735255 Lyz2 lysozyme 2 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20180906 MGI PMID:28476751 735255 Lyz2 lysozyme 2 gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:23204105 735255 Lyz2 lysozyme 2 gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:23204105 735255 Lyz2 lysozyme 2 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20180405 MGI PMID:24739962 735255 Lyz2 lysozyme 2 gene MP:0010064 increased circulating creatine level IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0010097 abnormal retina blood vessel morphology IAGP N RGD:5509061 20210121 MGI PMID:32668247 735255 Lyz2 lysozyme 2 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20210121 MGI PMID:32668247 735255 Lyz2 lysozyme 2 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20150917 MGI PMID:24995976 735255 Lyz2 lysozyme 2 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20190502 MGI PMID:27096368 735255 Lyz2 lysozyme 2 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20200806 MGI PMID:31285585 735255 Lyz2 lysozyme 2 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20210204 MGI PMID:22586041 735255 Lyz2 lysozyme 2 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20180920 MGI PMID:29263322 735255 Lyz2 lysozyme 2 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20457873 735255 Lyz2 lysozyme 2 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21930766 735255 Lyz2 lysozyme 2 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:24122813 735255 Lyz2 lysozyme 2 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20151015 MGI PMID:19933310 735255 Lyz2 lysozyme 2 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:19286998 735255 Lyz2 lysozyme 2 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:22201685 735255 Lyz2 lysozyme 2 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:23460747 735255 Lyz2 lysozyme 2 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20180830 MGI PMID:28771483 735255 Lyz2 lysozyme 2 gene MP:0010762 abnormal microglial cell activation IAGP N RGD:5509061 20150625 MGI PMID:25698726 735255 Lyz2 lysozyme 2 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19913445 735255 Lyz2 lysozyme 2 gene MP:0010812 absent type II pneumocytes IAGP N RGD:5509061 20141003 MGI PMID:17404282 735255 Lyz2 lysozyme 2 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20190926 MGI PMID:31126966 735255 Lyz2 lysozyme 2 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20180426 MGI PMID:28287403 735255 Lyz2 lysozyme 2 gene MP:0010873 decreased trabecular bone mass IAGP N RGD:5509061 20180426 MGI PMID:28287403 735255 Lyz2 lysozyme 2 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:21876000 735255 Lyz2 lysozyme 2 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20151015 MGI PMID:19933310 735255 Lyz2 lysozyme 2 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:21876000 735255 Lyz2 lysozyme 2 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20180426 MGI PMID:28287403 735255 Lyz2 lysozyme 2 gene MP:0010922 alveolitis IAGP N RGD:5509061 20141003 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20150917 MGI PMID:24995976 735255 Lyz2 lysozyme 2 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:23290137 735255 Lyz2 lysozyme 2 gene MP:0010962 decreased compact bone mass IAGP N RGD:5509061 20141003 MGI PMID:20053716 735255 Lyz2 lysozyme 2 gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:22101429 735255 Lyz2 lysozyme 2 gene MP:0011075 abnormal macrophage activation involved in immune response IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20210610 MGI PMID:31826938 735255 Lyz2 lysozyme 2 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20240613 MGI PMID:29101251 735255 Lyz2 lysozyme 2 gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12202685 735255 Lyz2 lysozyme 2 gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18988889 735255 Lyz2 lysozyme 2 gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:24302768 735255 Lyz2 lysozyme 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20308544 735255 Lyz2 lysozyme 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17476360 735255 Lyz2 lysozyme 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19501000 735255 Lyz2 lysozyme 2 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0011369 increased renal glomerulus apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:21135166 735255 Lyz2 lysozyme 2 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20170420 MGI PMID:23223452 735255 Lyz2 lysozyme 2 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210211 MGI PMID:22491258 735255 Lyz2 lysozyme 2 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210218 MGI PMID:17404282 735255 Lyz2 lysozyme 2 gene MP:0012007 abnormal chloride level IAGP N RGD:5509061 20141003 MGI PMID:23722907 735255 Lyz2 lysozyme 2 gene MP:0012441 abnormal monocyte cell number IAGP N RGD:5509061 20161103 MGI PMID:23637179 735255 Lyz2 lysozyme 2 gene MP:0013026 decreased Ly6C low monocyte number IAGP N RGD:5509061 20170413 MGI PMID:27814941 735255 Lyz2 lysozyme 2 gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20180830 MGI PMID:28771483 735255 Lyz2 lysozyme 2 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20180426 MGI PMID:28287403 735255 Lyz2 lysozyme 2 gene MP:0013661 abnormal myeloid cell number IAGP N RGD:5509061 20180906 MGI PMID:28476751 735255 Lyz2 lysozyme 2 gene MP:0014226 abnormal alveolar macrophage physiology IAGP N RGD:5509061 20180531 MGI PMID:28533230 735255 Lyz2 lysozyme 2 gene MP:0014229 decreased alveolar macrophage number IAGP N RGD:5509061 20180531 MGI PMID:28533230 735255 Lyz2 lysozyme 2 gene MP:0014434 decreased cytokine level IAGP N RGD:5509061 20240530 MGI PMID:38478630 735255 Lyz2 lysozyme 2 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20220120 MGI PMID:33859201 735255 Lyz2 lysozyme 2 gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20151015 MGI PMID:19933310 735255 Lyz2 lysozyme 2 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20210617 MGI PMID:31883536 735255 Lyz2 lysozyme 2 gene MP:0020849 abnormal actin cytoskeleton morphology IAGP N RGD:5509061 20200806 MGI PMID:31285585 735255 Lyz2 lysozyme 2 gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20240613 MGI PMID:29101251 735255 Lyz2 lysozyme 2 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20201210 MGI PMID:31320558 735255 Lyz2 lysozyme 2 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20230105 MGI PMID:36217001 735255 Lyz2 lysozyme 2 gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:29871919 735255 Lyz2 lysozyme 2 gene MP:0020953 decreased susceptibility to Paramyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:19398754 735255 Lyz2 lysozyme 2 gene MP:0020954 decreased mechanical nociceptive threshold IAGP N RGD:5509061 20220922 MGI PMID:34921782 735255 Lyz2 lysozyme 2 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:24553140 735255 Lyz2 lysozyme 2 gene MP:0030951 abnormal endocytosis IAGP N RGD:5509061 20191003 MGI PMID:31189603 735255 Lyz2 lysozyme 2 gene MP:0031024 increased susceptibility to Riboviria infection induced morbidity/mortality IAGP N RGD:5509061 20240613 MGI PMID:29101251 735255 Lyz2 lysozyme 2 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20201210 MGI PMID:31320558 735255 Lyz2 lysozyme 2 gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20230105 MGI PMID:36217001 735255 Lyz2 lysozyme 2 gene MP:0031113 pulmonary parenchymal consolidation IAGP N RGD:5509061 20200806 MGI PMID:31285585 735255 Lyz2 lysozyme 2 gene MP:0031220 increased circulating CXCL10 level IAGP N RGD:5509061 20210204 MGI PMID:31285585 735255 Lyz2 lysozyme 2 gene MP:0031225 decreased CXCL10 level IAGP N RGD:5509061 20210204 MGI PMID:22586041 735255 Lyz2 lysozyme 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:24995976 735255 Lyz2 lysozyme 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20240530 MGI PMID:38478630 735256 Tmod1 tropomodulin 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:12543641 735256 Tmod1 tropomodulin 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:14657235 735256 Tmod1 tropomodulin 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:12543641 735256 Tmod1 tropomodulin 1 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12543641 735256 Tmod1 tropomodulin 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12543641 735256 Tmod1 tropomodulin 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:14657235 735256 Tmod1 tropomodulin 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:14657235 735256 Tmod1 tropomodulin 1 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:14657235 735256 Tmod1 tropomodulin 1 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 735256 Tmod1 tropomodulin 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12543641 735256 Tmod1 tropomodulin 1 gene MP:0001627 abnormal cardiac output IAGP N RGD:5509061 20141003 MGI PMID:14657235 735256 Tmod1 tropomodulin 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:12543641 735256 Tmod1 tropomodulin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14657235 735256 Tmod1 tropomodulin 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:14657235 735256 Tmod1 tropomodulin 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12543641 735256 Tmod1 tropomodulin 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:12543641 735256 Tmod1 tropomodulin 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12543641 735256 Tmod1 tropomodulin 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:14657235 735256 Tmod1 tropomodulin 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20160804 MGI 735256 Tmod1 tropomodulin 1 gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14657235 735256 Tmod1 tropomodulin 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20180125 MGI PMID:12543641 735256 Tmod1 tropomodulin 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12543641 735256 Tmod1 tropomodulin 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14657235 735256 Tmod1 tropomodulin 1 gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:14657235 735256 Tmod1 tropomodulin 1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:14657235 735256 Tmod1 tropomodulin 1 gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12543641 735256 Tmod1 tropomodulin 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:12543641 735256 Tmod1 tropomodulin 1 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:14657235 735256 Tmod1 tropomodulin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12543641 735256 Tmod1 tropomodulin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14657235 735256 Tmod1 tropomodulin 1 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:14657235 735256 Tmod1 tropomodulin 1 gene MP:0012176 abnormal head development IAGP N RGD:5509061 20141003 MGI PMID:14657235 735258 Nudt6 nudix hydrolase 6 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20231207 MGI 735258 Nudt6 nudix hydrolase 6 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20231207 MGI 735261 Ces1d carboxylesterase 1D gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 735261 Ces1d carboxylesterase 1D gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 735261 Ces1d carboxylesterase 1D gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 735261 Ces1d carboxylesterase 1D gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 735261 Ces1d carboxylesterase 1D gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0003949 abnormal circulating lipid level IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 735261 Ces1d carboxylesterase 1D gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0008528 polycystic kidney IEA N RGD:5509061 20181227 MGI 735261 Ces1d carboxylesterase 1D gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:20197051 735261 Ces1d carboxylesterase 1D gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:20197051 735263 Gpr37 G protein-coupled receptor 37 gene MP:0000836 abnormal substantia nigra morphology IAGP N RGD:5509061 20141003 MGI PMID:15218106 735263 Gpr37 G protein-coupled receptor 37 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:15218106 735263 Gpr37 G protein-coupled receptor 37 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15218106 735263 Gpr37 G protein-coupled receptor 37 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17889953 735263 Gpr37 G protein-coupled receptor 37 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15218106 735263 Gpr37 G protein-coupled receptor 37 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15218106 735263 Gpr37 G protein-coupled receptor 37 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17889953 735263 Gpr37 G protein-coupled receptor 37 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17889953 735263 Gpr37 G protein-coupled receptor 37 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:17889953 735263 Gpr37 G protein-coupled receptor 37 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:17889953 735263 Gpr37 G protein-coupled receptor 37 gene MP:0005458 increased percent body fat/body weight IEA N RGD:5509061 20111116 MGI 735263 Gpr37 G protein-coupled receptor 37 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:15218106 735263 Gpr37 G protein-coupled receptor 37 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:17889953 735263 Gpr37 G protein-coupled receptor 37 gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17889953 735271 Hnrnpa1 heterogeneous nuclear ribonucleoprotein A1 gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20170202 MGI PMID:28077597 735271 Hnrnpa1 heterogeneous nuclear ribonucleoprotein A1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20170202 MGI PMID:28077597 735271 Hnrnpa1 heterogeneous nuclear ribonucleoprotein A1 gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20170202 MGI PMID:28077597 735271 Hnrnpa1 heterogeneous nuclear ribonucleoprotein A1 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20170202 MGI PMID:28077597 735271 Hnrnpa1 heterogeneous nuclear ribonucleoprotein A1 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20170202 MGI PMID:28077597 735271 Hnrnpa1 heterogeneous nuclear ribonucleoprotein A1 gene MP:0004070 abnormal P wave IAGP N RGD:5509061 20170202 MGI PMID:28077597 735271 Hnrnpa1 heterogeneous nuclear ribonucleoprotein A1 gene MP:0004136 abnormal tongue muscle morphology IAGP N RGD:5509061 20170202 MGI PMID:28077597 735271 Hnrnpa1 heterogeneous nuclear ribonucleoprotein A1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20170202 MGI PMID:28077597 735271 Hnrnpa1 heterogeneous nuclear ribonucleoprotein A1 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20170202 MGI PMID:28077597 735271 Hnrnpa1 heterogeneous nuclear ribonucleoprotein A1 gene MP:0010511 shortened PR interval IAGP N RGD:5509061 20170202 MGI PMID:28077597 735271 Hnrnpa1 heterogeneous nuclear ribonucleoprotein A1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170202 MGI PMID:28077597 735271 Hnrnpa1 heterogeneous nuclear ribonucleoprotein A1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170202 MGI PMID:28077597 735271 Hnrnpa1 heterogeneous nuclear ribonucleoprotein A1 gene MP:0030421 tongue muscle hypoplasia IAGP N RGD:5509061 20171214 MGI PMID:28077597 735274 Dlat dihydrolipoamide S-acetyltransferase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 735274 Dlat dihydrolipoamide S-acetyltransferase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20230601 MGI 735274 Dlat dihydrolipoamide S-acetyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735275 Snap91 synaptosomal-associated protein 91 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0001513 limb grasping IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0002083 premature death IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 735275 Snap91 synaptosomal-associated protein 91 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0020358 abnormal inhibitory synapse morphology IAGP N RGD:5509061 20161222 MGI PMID:26412491 735275 Snap91 synaptosomal-associated protein 91 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:26412491 735277 Cntn4 contactin 4 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18367085 735280 Rps6 ribosomal protein S6 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10856218 735280 Rps6 ribosomal protein S6 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16166381 735280 Rps6 ribosomal protein S6 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 735280 Rps6 ribosomal protein S6 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16166381 735280 Rps6 ribosomal protein S6 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16166381 735280 Rps6 ribosomal protein S6 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:16166381 735280 Rps6 ribosomal protein S6 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:16166381 735280 Rps6 ribosomal protein S6 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:10856218 735280 Rps6 ribosomal protein S6 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:16166381 735280 Rps6 ribosomal protein S6 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:16166381 735280 Rps6 ribosomal protein S6 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16166381 735280 Rps6 ribosomal protein S6 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16166381 735280 Rps6 ribosomal protein S6 gene MP:0005409 darkened coat color IAGP N RGD:5509061 20181227 MGI PMID:18641651 735280 Rps6 ribosomal protein S6 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:10856218 735280 Rps6 ribosomal protein S6 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16166381 735280 Rps6 ribosomal protein S6 gene MP:0009385 abnormal dermal pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 735280 Rps6 ribosomal protein S6 gene MP:0009387 abnormal epidermal pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 735280 Rps6 ribosomal protein S6 gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 735280 Rps6 ribosomal protein S6 gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 735280 Rps6 ribosomal protein S6 gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 735280 Rps6 ribosomal protein S6 gene MP:0011627 decreased skin pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 735280 Rps6 ribosomal protein S6 gene MP:0020221 reduced foot pad pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 735282 Col10a1 collagen, type X, alpha 1 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9015315 735282 Col10a1 collagen, type X, alpha 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9015315 735282 Col10a1 collagen, type X, alpha 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19834559 735282 Col10a1 collagen, type X, alpha 1 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20151126 MGI PMID:22692895 735282 Col10a1 collagen, type X, alpha 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20181227 MGI PMID:30010889 735282 Col10a1 collagen, type X, alpha 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20181227 MGI PMID:30010889 735282 Col10a1 collagen, type X, alpha 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:19834559 735282 Col10a1 collagen, type X, alpha 1 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20181227 MGI PMID:30010889 735282 Col10a1 collagen, type X, alpha 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20676705 735282 Col10a1 collagen, type X, alpha 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9015315 735282 Col10a1 collagen, type X, alpha 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:19834559 735282 Col10a1 collagen, type X, alpha 1 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:19834559 735282 Col10a1 collagen, type X, alpha 1 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20151126 MGI PMID:22692895 735282 Col10a1 collagen, type X, alpha 1 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20181227 MGI PMID:30010889 735282 Col10a1 collagen, type X, alpha 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:9015315 735282 Col10a1 collagen, type X, alpha 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19834559 735282 Col10a1 collagen, type X, alpha 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20181227 MGI PMID:30010889 735282 Col10a1 collagen, type X, alpha 1 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:7842010 735282 Col10a1 collagen, type X, alpha 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:19834559 735282 Col10a1 collagen, type X, alpha 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20151126 MGI PMID:22692895 735282 Col10a1 collagen, type X, alpha 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20151126 MGI PMID:22692895 735282 Col10a1 collagen, type X, alpha 1 gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20151126 MGI PMID:22692895 735282 Col10a1 collagen, type X, alpha 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:20676705 735282 Col10a1 collagen, type X, alpha 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20181227 MGI PMID:30010889 735282 Col10a1 collagen, type X, alpha 1 gene MP:0008477 decreased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19834559 735282 Col10a1 collagen, type X, alpha 1 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20151126 MGI PMID:22692895 735282 Col10a1 collagen, type X, alpha 1 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20151126 MGI PMID:22692895 735282 Col10a1 collagen, type X, alpha 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20151126 MGI PMID:22692895 735282 Col10a1 collagen, type X, alpha 1 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20151126 MGI PMID:22692895 735282 Col10a1 collagen, type X, alpha 1 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20151126 MGI PMID:22692895 735282 Col10a1 collagen, type X, alpha 1 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20676705 735282 Col10a1 collagen, type X, alpha 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:9015315 735282 Col10a1 collagen, type X, alpha 1 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20151126 MGI PMID:22692895 735282 Col10a1 collagen, type X, alpha 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10811836 735282 Col10a1 collagen, type X, alpha 1 gene MP:0013763 increased T-helper cell number IAGP N RGD:5509061 20151126 MGI PMID:22692895 735282 Col10a1 collagen, type X, alpha 1 gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20181227 MGI PMID:30010889 735282 Col10a1 collagen, type X, alpha 1 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20151126 MGI PMID:22692895 735282 Col10a1 collagen, type X, alpha 1 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20161013 MGI PMID:19834559 735282 Col10a1 collagen, type X, alpha 1 gene MP:0020354 increased endoplasmic reticulum stress IAGP N RGD:5509061 20181227 MGI PMID:30010889 735282 Col10a1 collagen, type X, alpha 1 gene MP:0030790 coxa vara IAGP N RGD:5509061 20181011 MGI PMID:9015315 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22201685 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000316 cellular necrosis IAGP N RGD:5509061 20141003 MGI PMID:22322302 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000566 synostosis IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19454673 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20201022 MGI 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23772036 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23772036 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0002044 increased colon adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22201685 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20201022 MGI 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:22322302 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19454673 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0003060 increased aerobic running capacity IAGP N RGD:5509061 20191024 MGI PMID:31519904 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:22322302 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:22322302 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:22201685 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:19454673 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0004064 decreased susceptibility to induced muscular atrophy IAGP N RGD:5509061 20191024 MGI PMID:31519904 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22201685 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0004560 abnormal chorionic plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0004575 small limb buds IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0004678 split xiphoid process IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:24166976 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:19454673 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:19454673 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:19454673 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19454673 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24166976 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20191024 MGI PMID:31519904 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:22201685 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20191024 MGI PMID:31519904 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20201022 MGI 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19454673 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19454673 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19454673 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:22201685 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22201685 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:22201685 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008617 increased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:22201685 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:22201685 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:22201685 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008959 abnormal spongiotrophoblast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20191024 MGI PMID:31519904 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22201685 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0009323 abnormal spleen development IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20191024 MGI PMID:31519904 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0009511 distended stomach IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22201685 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:24166976 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20191024 MGI PMID:31519904 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:22201685 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20191024 MGI PMID:31519904 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19884656 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:19307312 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0012107 enhanced exercise endurance IAGP N RGD:5509061 20191024 MGI PMID:31519904 735284 Elavl1 ELAV like RNA binding protein 1 gene MP:0014078 small intestinal villus atrophy IAGP N RGD:5509061 20160310 MGI PMID:19884656 735293 Pgc progastricsin (pepsinogen C) gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240523 MGI 735293 Pgc progastricsin (pepsinogen C) gene MP:0000274 enlarged heart IEA N RGD:5509061 20240523 MGI 735293 Pgc progastricsin (pepsinogen C) gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20231109 MGI PMID:37291517 735293 Pgc progastricsin (pepsinogen C) gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 735293 Pgc progastricsin (pepsinogen C) gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 735293 Pgc progastricsin (pepsinogen C) gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20240523 MGI 735293 Pgc progastricsin (pepsinogen C) gene MP:0001147 small testis IEA N RGD:5509061 20240523 MGI 735293 Pgc progastricsin (pepsinogen C) gene MP:0002083 premature death IAGP N RGD:5509061 20231109 MGI PMID:37291517 735293 Pgc progastricsin (pepsinogen C) gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20231109 MGI PMID:37291517 735293 Pgc progastricsin (pepsinogen C) gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20231109 MGI PMID:37291517 735293 Pgc progastricsin (pepsinogen C) gene MP:0002966 decreased circulating alkaline phosphatase level IAGP N RGD:5509061 20231109 MGI PMID:37291517 735293 Pgc progastricsin (pepsinogen C) gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20231109 MGI PMID:37291517 735293 Pgc progastricsin (pepsinogen C) gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16094689 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8036519 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20160804 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16094689 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:16094689 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:16094689 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:8036519 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8036519 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:12176324 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:12176324 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:12176324 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23650205 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16094689 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:14978086 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:18628996 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16094689 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8036519 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002281 abnormal respiratory mucosa goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12626595 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002334 abnormal airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:11801688 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:12626595 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:8036519 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:8036519 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11069247 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15356099 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11801688 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:11801688 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:15466624 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16094689 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:23650205 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20141003 MGI PMID:11801688 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11801688 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:16094689 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:10951241 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11714818 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:19109198 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:14978086 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:16941672 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:14978086 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:16094689 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:16094689 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0004794 increased anti-nuclear antigen antibody level IEA N RGD:5509061 20201022 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0004909 increased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:16094689 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0004928 increased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:16094689 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16094689 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16094689 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:16094689 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20201231 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:8036519 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20181227 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005018 decreased T cell number IEA N RGD:5509061 20201231 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:11714818 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005398 decreased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:11801688 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:11801688 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:11801688 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005478 decreased circulating thyroxine level IEA N RGD:5509061 20210128 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20211021 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:14707102 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:18628996 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210128 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11123307 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:8036519 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008209 decreased pre-B cell number IEA N RGD:5509061 20201231 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008211 decreased mature B cell number IEA N RGD:5509061 20201231 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008215 decreased immature B cell number IEA N RGD:5509061 20201231 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008346 increased gamma-delta T cell number IEA N RGD:5509061 20141003 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008542 enlarged cervical lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8036519 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:8036519 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:10951241 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:11046063 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:15385471 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:11069247 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:11714818 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:8036519 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:11801688 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:11801688 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:14707102 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:14500678 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:24509076 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20210128 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8036519 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IEA N RGD:5509061 20201022 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0010838 increased CD8-positive, alpha-beta memory T cell number IEA N RGD:5509061 20201022 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0011225 lymph node medullary cord hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8036519 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0011816 decreased pre-pro B cell number IEA N RGD:5509061 20201231 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0013022 increased Ly6C high monocyte number IEA N RGD:5509061 20181227 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0013025 increased Ly6C low monocyte number IEA N RGD:5509061 20181227 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0013154 increased KLRG1+ CD8 alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0013157 increased KLRG1+ CD4 alpha-beta T cell number IEA N RGD:5509061 20201022 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0013418 increased memory-marker gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0013427 increased memory-marker NK cell number IEA N RGD:5509061 20201231 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0013523 increased memory-marker CD4-positive NK T cell number IEA N RGD:5509061 20201231 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0013654 increased CD103-positive CD11b-low dendritic cell number IEA N RGD:5509061 20201231 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20201231 MGI 735300 Cxcr2 C-X-C motif chemokine receptor 2 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:14707102 735303 Rida reactive intermediate imine deaminase A homolog gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 735303 Rida reactive intermediate imine deaminase A homolog gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20181227 MGI 735303 Rida reactive intermediate imine deaminase A homolog gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20201231 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0000452 abnormal mouth morphology IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0000520 absent kidney IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:16061793 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0000564 syndactyly IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20190523 MGI PMID:15314648 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16061793 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19666503 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15755804 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15755804 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0002132 abnormal respiratory system morphology IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19666503 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:16061793 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0002639 micrognathia IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20190523 MGI PMID:15314648 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0003321 tracheoesophageal fistula IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0004017 duplex kidney IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0004131 abnormal motile primary cilium morphology IEA N RGD:5509061 20210916 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:16061793 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0005157 holoprosencephaly IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0006197 ocular hypotelorism IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0010406 common atrium IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0010413 complete atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0010476 coronary fistula IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0010551 abnormal coronary vessel morphology IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0010635 aorta pulmonary collateral arteries IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0010975 abnormal lung lobe morphology IEA N RGD:5509061 20141003 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16061793 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0011671 balanced complete atrioventricular canal IEA N RGD:5509061 20210708 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0011672 unbalanced complete atrioventricular canal, left dominant IEA N RGD:5509061 20210708 MGI 735308 Dync2h1 dynein cytoplasmic 2 heavy chain 1 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:18488998 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18172198 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11679434 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11679434 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8757131 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:9570795 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:18172198 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:8757131 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:8757131 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0002310 decreased susceptibility to hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11679434 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0003136 yellow coat color IAGP N RGD:5509061 20141003 MGI PMID:18172198 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11679434 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11679434 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11679434 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:8757131 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:11679434 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:8757131 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:18172198 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18172198 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18172198 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:8757131 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:11679434 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:8757131 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11679434 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18172198 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:8757131 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18172198 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18172198 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18172198 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11679434 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:9570795 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:23569242 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:11679434 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:8757131 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:18172198 735311 Prkar2b protein kinase, cAMP dependent regulatory, type II beta gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:23569242 735312 Mc3r melanocortin 3 receptor gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220519 MGI 735312 Mc3r melanocortin 3 receptor gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 735312 Mc3r melanocortin 3 receptor gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 735312 Mc3r melanocortin 3 receptor gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:10973258 735312 Mc3r melanocortin 3 receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:10965927 735312 Mc3r melanocortin 3 receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:10973258 735312 Mc3r melanocortin 3 receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:10965927 735312 Mc3r melanocortin 3 receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10973258 735312 Mc3r melanocortin 3 receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21984834 735312 Mc3r melanocortin 3 receptor gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:10973258 735312 Mc3r melanocortin 3 receptor gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:21984834 735312 Mc3r melanocortin 3 receptor gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 735312 Mc3r melanocortin 3 receptor gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:10973258 735312 Mc3r melanocortin 3 receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:10973258 735312 Mc3r melanocortin 3 receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21984834 735312 Mc3r melanocortin 3 receptor gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 735312 Mc3r melanocortin 3 receptor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21984834 735312 Mc3r melanocortin 3 receptor gene MP:0002834 decreased heart weight IEA N RGD:5509061 20211021 MGI 735312 Mc3r melanocortin 3 receptor gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 735312 Mc3r melanocortin 3 receptor gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:10973258 735312 Mc3r melanocortin 3 receptor gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:21984834 735312 Mc3r melanocortin 3 receptor gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:10973258 735312 Mc3r melanocortin 3 receptor gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:21984834 735312 Mc3r melanocortin 3 receptor gene MP:0004129 abnormal respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:10965927 735312 Mc3r melanocortin 3 receptor gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:21984834 735312 Mc3r melanocortin 3 receptor gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21984834 735312 Mc3r melanocortin 3 receptor gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:10965927 735312 Mc3r melanocortin 3 receptor gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21984834 735312 Mc3r melanocortin 3 receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18719666 735312 Mc3r melanocortin 3 receptor gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:10973258 735312 Mc3r melanocortin 3 receptor gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:21984834 735312 Mc3r melanocortin 3 receptor gene MP:0005667 abnormal circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21984834 735312 Mc3r melanocortin 3 receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:10973258 735312 Mc3r melanocortin 3 receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21984834 735312 Mc3r melanocortin 3 receptor gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10973258 735312 Mc3r melanocortin 3 receptor gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:10973258 735312 Mc3r melanocortin 3 receptor gene MP:0009128 decreased brown fat cell number IAGP N RGD:5509061 20141003 MGI PMID:10973258 735312 Mc3r melanocortin 3 receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:10965927 735312 Mc3r melanocortin 3 receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:10973258 735312 Mc3r melanocortin 3 receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21984834 735312 Mc3r melanocortin 3 receptor gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220519 MGI 735312 Mc3r melanocortin 3 receptor gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20190725 MGI PMID:21984834 735312 Mc3r melanocortin 3 receptor gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:15034587 735312 Mc3r melanocortin 3 receptor gene MP:0012320 abnormal body fat mass IAGP N RGD:5509061 20160407 MGI PMID:21984834 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:24036948 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:19931571 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18096591 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:24036948 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20200402 MGI PMID:27224030 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20200521 MGI PMID:30557356 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20200402 MGI PMID:27224030 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:19931571 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:15964986 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:17167076 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:19931571 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:24036948 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20141003 MGI PMID:24036948 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:17167076 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20150122 MGI PMID:18270172 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:24036948 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20200402 MGI PMID:27224030 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:24036948 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:24036948 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200402 MGI PMID:27224030 735313 Scn11a sodium channel, voltage-gated, type XI, alpha gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200521 MGI PMID:30557356 735314 Pla2g2c phospholipase A2, group IIC gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 735318 Adgrg2 adhesion G protein-coupled receptor G2 gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:15367682 735318 Adgrg2 adhesion G protein-coupled receptor G2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15367682 735318 Adgrg2 adhesion G protein-coupled receptor G2 gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:15367682 735318 Adgrg2 adhesion G protein-coupled receptor G2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15367682 735318 Adgrg2 adhesion G protein-coupled receptor G2 gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:15367682 735318 Adgrg2 adhesion G protein-coupled receptor G2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15367682 735318 Adgrg2 adhesion G protein-coupled receptor G2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15367682 735318 Adgrg2 adhesion G protein-coupled receptor G2 gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:15367682 735318 Adgrg2 adhesion G protein-coupled receptor G2 gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:15367682 735318 Adgrg2 adhesion G protein-coupled receptor G2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15367682 735318 Adgrg2 adhesion G protein-coupled receptor G2 gene MP:0009140 dilated efferent ductule of testis IAGP N RGD:5509061 20141003 MGI PMID:15367682 735318 Adgrg2 adhesion G protein-coupled receptor G2 gene MP:0009234 absent sperm head IAGP N RGD:5509061 20141003 MGI PMID:15367682 735318 Adgrg2 adhesion G protein-coupled receptor G2 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:15367682 735318 Adgrg2 adhesion G protein-coupled receptor G2 gene MP:0009257 dilated seminiferous tubule IAGP N RGD:5509061 20141003 MGI PMID:15367682 735322 P2rx3 purinergic receptor P2X, ligand-gated ion channel, 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:14672995 735322 P2rx3 purinergic receptor P2X, ligand-gated ion channel, 3 gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:11069182 735322 P2rx3 purinergic receptor P2X, ligand-gated ion channel, 3 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11069182 735322 P2rx3 purinergic receptor P2X, ligand-gated ion channel, 3 gene MP:0002735 abnormal chemical nociception IAGP N RGD:5509061 20141003 MGI PMID:11069182 735322 P2rx3 purinergic receptor P2X, ligand-gated ion channel, 3 gene MP:0003438 abnormal carotid body physiology IAGP N RGD:5509061 20141003 MGI PMID:14672995 735322 P2rx3 purinergic receptor P2X, ligand-gated ion channel, 3 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:11069182 735322 P2rx3 purinergic receptor P2X, ligand-gated ion channel, 3 gene MP:0005576 decreased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:14672995 735322 P2rx3 purinergic receptor P2X, ligand-gated ion channel, 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:14672995 735322 P2rx3 purinergic receptor P2X, ligand-gated ion channel, 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14672995 735327 Asz1 ankyrin repeat, SAM and basic leucine zipper domain containing 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19730684 735327 Asz1 ankyrin repeat, SAM and basic leucine zipper domain containing 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19730684 735327 Asz1 ankyrin repeat, SAM and basic leucine zipper domain containing 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19730684 735327 Asz1 ankyrin repeat, SAM and basic leucine zipper domain containing 1 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:19730684 735327 Asz1 ankyrin repeat, SAM and basic leucine zipper domain containing 1 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19730684 735327 Asz1 ankyrin repeat, SAM and basic leucine zipper domain containing 1 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:19730684 735327 Asz1 ankyrin repeat, SAM and basic leucine zipper domain containing 1 gene MP:0008878 abnormal DNA methylation during gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:19730684 735334 Galr3 galanin receptor 3 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160519 MGI PMID:24782539 735334 Galr3 galanin receptor 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20160519 MGI PMID:24782539 735334 Galr3 galanin receptor 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160519 MGI PMID:24782539 735334 Galr3 galanin receptor 3 gene MP:0003982 increased cholesterol level IEA N RGD:5509061 20141003 MGI 735334 Galr3 galanin receptor 3 gene MP:0005317 increased triglyceride level IEA N RGD:5509061 20141003 MGI 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12782654 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:12782654 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:12782654 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:15713628 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:15713641 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20201022 MGI PMID:31194862 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:11544177 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12782654 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:11544177 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:11544177 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:11544177 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11544177 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:12782654 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:12782654 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20201022 MGI PMID:31194862 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001238 thin epidermis stratum spinosum IAGP N RGD:5509061 20141003 MGI PMID:12782654 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11533044 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11544177 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16923958 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15713641 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16923958 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19289493 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20201022 MGI PMID:31194862 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19289493 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17442925 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17442925 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17210696 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001884 mammary gland alveolar hyperplasia IAGP N RGD:5509061 20201022 MGI PMID:31194862 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12782654 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:11544177 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19289493 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12782654 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11544177 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12782654 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15713641 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17442925 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12782654 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11544177 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21906027 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19289493 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20201022 MGI PMID:31194862 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0003266 biliary cyst IAGP N RGD:5509061 20201022 MGI PMID:31194862 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:19289493 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0004126 thin hypodermis IAGP N RGD:5509061 20141003 MGI PMID:15713628 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:15713641 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442925 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17442925 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19289493 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:19289493 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19289493 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17442925 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21906027 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:14745448 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19289493 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:12782654 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20201022 MGI PMID:31194862 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:12782654 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11533044 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16923958 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0012109 decreased trophoblast glycogen cell number IAGP N RGD:5509061 20141003 MGI PMID:12783884 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0014057 abnormal mammary gland stroma morphology IAGP N RGD:5509061 20201022 MGI PMID:31194862 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0014171 increased fatty acid oxidation IAGP N RGD:5509061 20160421 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:11544177 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:22037765 735336 Akt1 thymoma viral proto-oncogene 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:22037765 735337 Pctp phosphatidylcholine transfer protein gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17046758 735337 Pctp phosphatidylcholine transfer protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10500206 735337 Pctp phosphatidylcholine transfer protein gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15628972 735337 Pctp phosphatidylcholine transfer protein gene MP:0002830 gallstones IAGP N RGD:5509061 20141003 MGI PMID:15576839 735337 Pctp phosphatidylcholine transfer protein gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15576839 735337 Pctp phosphatidylcholine transfer protein gene MP:0003983 decreased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15576839 735337 Pctp phosphatidylcholine transfer protein gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20141003 MGI PMID:15576839 735337 Pctp phosphatidylcholine transfer protein gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:15576839 735337 Pctp phosphatidylcholine transfer protein gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:15576839 735337 Pctp phosphatidylcholine transfer protein gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:15576839 735337 Pctp phosphatidylcholine transfer protein gene MP:0005085 abnormal gallbladder physiology IAGP N RGD:5509061 20141003 MGI PMID:15576839 735337 Pctp phosphatidylcholine transfer protein gene MP:0008991 abnormal bile canaliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:15576839 735337 Pctp phosphatidylcholine transfer protein gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15628972 735339 Rps28 ribosomal protein S28 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9784405 735340 Etfa electron transferring flavoprotein, alpha polypeptide gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 735340 Etfa electron transferring flavoprotein, alpha polypeptide gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 735344 Synpo synaptopodin gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:12928494 735344 Synpo synaptopodin gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12928494 735344 Synpo synaptopodin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12928494 735344 Synpo synaptopodin gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12928494 735344 Synpo synaptopodin gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12928494 735347 Jund jun D proto-oncogene gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15655111 735347 Jund jun D proto-oncogene gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11106750 735347 Jund jun D proto-oncogene gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10654608 735347 Jund jun D proto-oncogene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141016 MGI PMID:24411941 735347 Jund jun D proto-oncogene gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15655111 735347 Jund jun D proto-oncogene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10654608 735347 Jund jun D proto-oncogene gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15655111 735347 Jund jun D proto-oncogene gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11106750 735347 Jund jun D proto-oncogene gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10654608 735347 Jund jun D proto-oncogene gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15655111 735347 Jund jun D proto-oncogene gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10654608 735347 Jund jun D proto-oncogene gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:10654608 735347 Jund jun D proto-oncogene gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10654608 735347 Jund jun D proto-oncogene gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10654608 735347 Jund jun D proto-oncogene gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10654608 735347 Jund jun D proto-oncogene gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15655111 735347 Jund jun D proto-oncogene gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:11106750 735347 Jund jun D proto-oncogene gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141016 MGI PMID:24411941 735347 Jund jun D proto-oncogene gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20300111 735347 Jund jun D proto-oncogene gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:15655111 735347 Jund jun D proto-oncogene gene MP:0005120 decreased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:10654608 735347 Jund jun D proto-oncogene gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:10654608 735347 Jund jun D proto-oncogene gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141016 MGI PMID:24411941 735347 Jund jun D proto-oncogene gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:15655111 735347 Jund jun D proto-oncogene gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:15655111 735347 Jund jun D proto-oncogene gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15029240 735347 Jund jun D proto-oncogene gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:15029240 735347 Jund jun D proto-oncogene gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141016 MGI PMID:24411941 735347 Jund jun D proto-oncogene gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10654608 735347 Jund jun D proto-oncogene gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15655111 735347 Jund jun D proto-oncogene gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:15655111 735347 Jund jun D proto-oncogene gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:15655111 735347 Jund jun D proto-oncogene gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:20300111 735347 Jund jun D proto-oncogene gene MP:0008410 increased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:11106750 735347 Jund jun D proto-oncogene gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:11106750 735347 Jund jun D proto-oncogene gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141016 MGI PMID:24411941 735347 Jund jun D proto-oncogene gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141016 MGI PMID:24411941 735347 Jund jun D proto-oncogene gene MP:0010017 visceral vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15655111 735347 Jund jun D proto-oncogene gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15655111 735347 Jund jun D proto-oncogene gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15655111 735347 Jund jun D proto-oncogene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15655111 735347 Jund jun D proto-oncogene gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20300111 735347 Jund jun D proto-oncogene gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:11106750 735347 Jund jun D proto-oncogene gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20300111 735347 Jund jun D proto-oncogene gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:24411941 735350 Tnni1 troponin I, skeletal, slow 1 gene MP:0004357 long tibia IEA N RGD:5509061 20181227 MGI 735350 Tnni1 troponin I, skeletal, slow 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735351 Gpx2 glutathione peroxidase 2 gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20141003 MGI PMID:11518697 735351 Gpx2 glutathione peroxidase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11518697 735351 Gpx2 glutathione peroxidase 2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:11518697 735351 Gpx2 glutathione peroxidase 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11518697 735351 Gpx2 glutathione peroxidase 2 gene MP:0001858 intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:11518697 735351 Gpx2 glutathione peroxidase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11518697 735351 Gpx2 glutathione peroxidase 2 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:11518697 735351 Gpx2 glutathione peroxidase 2 gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:11518697 735351 Gpx2 glutathione peroxidase 2 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:11518697 735351 Gpx2 glutathione peroxidase 2 gene MP:0005035 perianal ulcer IAGP N RGD:5509061 20141003 MGI PMID:11518697 735351 Gpx2 glutathione peroxidase 2 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:11518697 735351 Gpx2 glutathione peroxidase 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:11518697 735351 Gpx2 glutathione peroxidase 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:11518697 735351 Gpx2 glutathione peroxidase 2 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:11518697 735351 Gpx2 glutathione peroxidase 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11518697 735352 Maf MAF bZIP transcription factor gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 735352 Maf MAF bZIP transcription factor gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 735352 Maf MAF bZIP transcription factor gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:22345400 735352 Maf MAF bZIP transcription factor gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:10603348 735352 Maf MAF bZIP transcription factor gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20201022 MGI 735352 Maf MAF bZIP transcription factor gene MP:0000601 small liver IEA N RGD:5509061 20201022 MGI 735352 Maf MAF bZIP transcription factor gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 735352 Maf MAF bZIP transcription factor gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 735352 Maf MAF bZIP transcription factor gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 735352 Maf MAF bZIP transcription factor gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12620964 735352 Maf MAF bZIP transcription factor gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:10603348 735352 Maf MAF bZIP transcription factor gene MP:0000982 abnormal Meissner's corpuscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22345400 735352 Maf MAF bZIP transcription factor gene MP:0000988 abnormal pacinian corpuscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22345400 735352 Maf MAF bZIP transcription factor gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 735352 Maf MAF bZIP transcription factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22345400 735352 Maf MAF bZIP transcription factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10097114 735352 Maf MAF bZIP transcription factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12620964 735352 Maf MAF bZIP transcription factor gene MP:0001288 abnormal lens induction IAGP N RGD:5509061 20141003 MGI PMID:12620964 735352 Maf MAF bZIP transcription factor gene MP:0001292 abnormal lens vesicle development IAGP N RGD:5509061 20141003 MGI PMID:10603348 735352 Maf MAF bZIP transcription factor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10097114 735352 Maf MAF bZIP transcription factor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:12620964 735352 Maf MAF bZIP transcription factor gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:10097114 735352 Maf MAF bZIP transcription factor gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:12620964 735352 Maf MAF bZIP transcription factor gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:10603348 735352 Maf MAF bZIP transcription factor gene MP:0001320 small pupil IAGP N RGD:5509061 20141003 MGI PMID:12620964 735352 Maf MAF bZIP transcription factor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22345400 735352 Maf MAF bZIP transcription factor gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:10603348 735352 Maf MAF bZIP transcription factor gene MP:0001614 abnormal blood vessel morphology IEA N RGD:5509061 20201022 MGI 735352 Maf MAF bZIP transcription factor gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 735352 Maf MAF bZIP transcription factor gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:12620964 735352 Maf MAF bZIP transcription factor gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 735352 Maf MAF bZIP transcription factor gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12620964 735352 Maf MAF bZIP transcription factor gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22345400 735352 Maf MAF bZIP transcription factor gene MP:0002638 abnormal pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:12620964 735352 Maf MAF bZIP transcription factor gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240627 MGI 735352 Maf MAF bZIP transcription factor gene MP:0002704 tubular nephritis IAGP N RGD:5509061 20141003 MGI PMID:12620964 735352 Maf MAF bZIP transcription factor gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:12620964 735352 Maf MAF bZIP transcription factor gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:10383433 735352 Maf MAF bZIP transcription factor gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 735352 Maf MAF bZIP transcription factor gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 735352 Maf MAF bZIP transcription factor gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210128 MGI 735352 Maf MAF bZIP transcription factor gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 735352 Maf MAF bZIP transcription factor gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210826 MGI 735352 Maf MAF bZIP transcription factor gene MP:0004848 abnormal liver size IEA N RGD:5509061 20230601 MGI 735352 Maf MAF bZIP transcription factor gene MP:0005301 abnormal cornea endothelium morphology IAGP N RGD:5509061 20160310 MGI PMID:10603348 735352 Maf MAF bZIP transcription factor gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 735352 Maf MAF bZIP transcription factor gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22345400 735352 Maf MAF bZIP transcription factor gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:22345400 735352 Maf MAF bZIP transcription factor gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:10097114 735352 Maf MAF bZIP transcription factor gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:10383433 735352 Maf MAF bZIP transcription factor gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:10603348 735352 Maf MAF bZIP transcription factor gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:10403649 735352 Maf MAF bZIP transcription factor gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:22345400 735352 Maf MAF bZIP transcription factor gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200514 MGI 735352 Maf MAF bZIP transcription factor gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20210520 MGI 735352 Maf MAF bZIP transcription factor gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 735352 Maf MAF bZIP transcription factor gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:17374726 735352 Maf MAF bZIP transcription factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10383433 735352 Maf MAF bZIP transcription factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12620964 735352 Maf MAF bZIP transcription factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10097114 735352 Maf MAF bZIP transcription factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10603348 735352 Maf MAF bZIP transcription factor gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12620964 735352 Maf MAF bZIP transcription factor gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10097114 735352 Maf MAF bZIP transcription factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735352 Maf MAF bZIP transcription factor gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10383433 735352 Maf MAF bZIP transcription factor gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10097114 735352 Maf MAF bZIP transcription factor gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20160310 MGI PMID:10603348 735352 Maf MAF bZIP transcription factor gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 735352 Maf MAF bZIP transcription factor gene MP:0030996 decreased pacinian corpuscle number IAGP N RGD:5509061 20200130 MGI PMID:22345400 735352 Maf MAF bZIP transcription factor gene MP:0030998 small pacinian corpuscles IAGP N RGD:5509061 20200130 MGI PMID:22345400 735354 Pcdh8 protocadherin 8 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10890978 735354 Pcdh8 protocadherin 8 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 735358 Usp2 ubiquitin specific peptidase 2 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:21543767 735358 Usp2 ubiquitin specific peptidase 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21966515 735358 Usp2 ubiquitin specific peptidase 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:21543767 735358 Usp2 ubiquitin specific peptidase 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21543767 735358 Usp2 ubiquitin specific peptidase 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21543767 735358 Usp2 ubiquitin specific peptidase 2 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 735358 Usp2 ubiquitin specific peptidase 2 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:21543767 735358 Usp2 ubiquitin specific peptidase 2 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21543767 735358 Usp2 ubiquitin specific peptidase 2 gene MP:0020468 abnormal circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:21966515 735358 Usp2 ubiquitin specific peptidase 2 gene MP:0020475 delayed circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:21966515 735359 Tcf4 transcription factor 4 gene MP:0000433 microcephaly IAGP N RGD:5509061 20180607 MGI PMID:29222403 735359 Tcf4 transcription factor 4 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11069067 735359 Tcf4 transcription factor 4 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11069067 735359 Tcf4 transcription factor 4 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20201231 MGI PMID:29588831 735359 Tcf4 transcription factor 4 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20201231 MGI PMID:29588831 735359 Tcf4 transcription factor 4 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:17878293 735359 Tcf4 transcription factor 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180607 MGI PMID:29222403 735359 Tcf4 transcription factor 4 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 735359 Tcf4 transcription factor 4 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20201231 MGI PMID:27568567 735359 Tcf4 transcription factor 4 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20180607 MGI PMID:29222403 735359 Tcf4 transcription factor 4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20201231 MGI PMID:27568567 735359 Tcf4 transcription factor 4 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20201231 MGI PMID:27568567 735359 Tcf4 transcription factor 4 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20201231 MGI PMID:27568567 735359 Tcf4 transcription factor 4 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20180607 MGI PMID:29222403 735359 Tcf4 transcription factor 4 gene MP:0001525 impaired balance IAGP N RGD:5509061 20201231 MGI PMID:27568567 735359 Tcf4 transcription factor 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8649400 735359 Tcf4 transcription factor 4 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11069067 735359 Tcf4 transcription factor 4 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18384878 735359 Tcf4 transcription factor 4 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20180607 MGI PMID:29222403 735359 Tcf4 transcription factor 4 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20180607 MGI PMID:29222403 735359 Tcf4 transcription factor 4 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18384878 735359 Tcf4 transcription factor 4 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20180607 MGI PMID:29222403 735359 Tcf4 transcription factor 4 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20201231 MGI PMID:27568567 735359 Tcf4 transcription factor 4 gene MP:0003234 enhanced NMDA-mediated synaptic currents IAGP N RGD:5509061 20180607 MGI PMID:29222403 735359 Tcf4 transcription factor 4 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:18384878 735359 Tcf4 transcription factor 4 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:11069067 735359 Tcf4 transcription factor 4 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20180607 MGI PMID:29222403 735359 Tcf4 transcription factor 4 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17878293 735359 Tcf4 transcription factor 4 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20201231 MGI PMID:29588831 735359 Tcf4 transcription factor 4 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:8649400 735359 Tcf4 transcription factor 4 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20201231 MGI PMID:27568567 735359 Tcf4 transcription factor 4 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20180607 MGI PMID:29222403 735359 Tcf4 transcription factor 4 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20180607 MGI PMID:29222403 735359 Tcf4 transcription factor 4 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20201231 MGI PMID:27568567 735359 Tcf4 transcription factor 4 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20201231 MGI PMID:27568567 735359 Tcf4 transcription factor 4 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20201231 MGI PMID:27568567 735359 Tcf4 transcription factor 4 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20201231 MGI PMID:27568567 735359 Tcf4 transcription factor 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18384878 735359 Tcf4 transcription factor 4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8649400 735359 Tcf4 transcription factor 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8649400 735359 Tcf4 transcription factor 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17878293 735359 Tcf4 transcription factor 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 735359 Tcf4 transcription factor 4 gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20180607 MGI PMID:29222403 735359 Tcf4 transcription factor 4 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20180607 MGI PMID:29222403 735359 Tcf4 transcription factor 4 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20201231 MGI PMID:27568567 735359 Tcf4 transcription factor 4 gene MP:0020083 decreased hippocampus volume IAGP N RGD:5509061 20201231 MGI PMID:29588831 735359 Tcf4 transcription factor 4 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20201231 MGI PMID:27568567 735359 Tcf4 transcription factor 4 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:27568567 735359 Tcf4 transcription factor 4 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:29222403 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10215630 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0000296 absent trabeculae carneae IAGP N RGD:5509061 20141003 MGI PMID:10215630 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:15829524 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15829524 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15829524 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15829524 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:15890675 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10215630 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:20147377 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:20147377 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:15855320 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15855320 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15875024 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:10215630 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:17404209 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:17404209 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15890675 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17404209 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20360386 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20360386 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10215630 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15875024 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17404209 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15890675 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:17404209 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20382891 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15890675 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15855320 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15855320 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:15890675 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:15829524 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:10215630 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0002725 abnormal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15875024 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15855320 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15855320 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:15829524 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:17404209 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:17404209 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15829524 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17404209 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:20147377 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0004784 abnormal anterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:10215630 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0004785 abnormal posterior cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:10215630 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:15890675 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20147377 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:20147377 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15855320 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15855320 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15855320 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15855320 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10215630 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:17404209 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17404209 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20161027 MGI PMID:15890675 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:15890675 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0009020 prolonged metestrus IAGP N RGD:5509061 20141003 MGI PMID:15890675 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0009021 absent estrus IAGP N RGD:5509061 20141003 MGI PMID:15890675 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0009085 abnormal uterine horn morphology IAGP N RGD:5509061 20141003 MGI PMID:15890675 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0009089 short uterine horn IAGP N RGD:5509061 20141003 MGI PMID:17404209 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:17404209 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0010198 decreased lymphatic vessel endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:20360386 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0010780 abnormal stomach smooth muscle circular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15829524 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0010785 abnormal stomach pyloric region morphology IAGP N RGD:5509061 20141003 MGI PMID:15829524 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10215630 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15855320 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15855320 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15875024 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10215630 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17404209 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20360386 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0011389 absent optic disk IAGP N RGD:5509061 20141003 MGI PMID:20147377 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0012535 abnormal optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:20147377 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0013575 abnormal forestomach-glandular stomach junction morphology IAGP N RGD:5509061 20150305 MGI PMID:15829524 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0013576 small forestomach IAGP N RGD:5509061 20150305 MGI PMID:15829524 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20191219 MGI PMID:17404209 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0031137 vaginal hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:17404209 735362 Nr2f2 nuclear receptor subfamily 2, group F, member 2 gene MP:0031434 increased miscarriage rate IAGP N RGD:5509061 20220915 MGI PMID:17404209 735364 P3h4 prolyl 3-hydroxylase family member 4 (non-enzymatic) gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20170810 MGI PMID:27119146 735364 P3h4 prolyl 3-hydroxylase family member 4 (non-enzymatic) gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20170810 MGI PMID:27119146 735364 P3h4 prolyl 3-hydroxylase family member 4 (non-enzymatic) gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20170810 MGI PMID:27119146 735364 P3h4 prolyl 3-hydroxylase family member 4 (non-enzymatic) gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20170810 MGI PMID:27119146 735364 P3h4 prolyl 3-hydroxylase family member 4 (non-enzymatic) gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20170810 MGI PMID:27119146 735364 P3h4 prolyl 3-hydroxylase family member 4 (non-enzymatic) gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20170810 MGI PMID:27119146 735364 P3h4 prolyl 3-hydroxylase family member 4 (non-enzymatic) gene MP:0011642 abnormal bone collagen fibril morphology IAGP N RGD:5509061 20170810 MGI PMID:27119146 735366 Urod uroporphyrinogen decarboxylase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11134514 735366 Urod uroporphyrinogen decarboxylase gene MP:0004147 increased porphyrin level IAGP N RGD:5509061 20141003 MGI PMID:11134514 735366 Urod uroporphyrinogen decarboxylase gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:11134514 735366 Urod uroporphyrinogen decarboxylase gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11134514 735368 Cma1 chymase 1, mast cell gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15905575 735370 Calm1 calmodulin 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20190711 MGI PMID:30322141 735370 Calm1 calmodulin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190711 MGI PMID:30322141 735370 Calm1 calmodulin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240509 MGI PMID:37589122 735370 Calm1 calmodulin 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20190711 MGI PMID:30322141 735370 Calm1 calmodulin 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20190711 MGI PMID:30322141 735370 Calm1 calmodulin 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20240509 MGI PMID:37589122 735370 Calm1 calmodulin 1 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20190711 MGI PMID:30322141 735370 Calm1 calmodulin 1 gene MP:0003060 increased aerobic running capacity IAGP N RGD:5509061 20190711 MGI PMID:30322141 735370 Calm1 calmodulin 1 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20240509 MGI PMID:37589122 735370 Calm1 calmodulin 1 gene MP:0003928 increased heart rate variability IAGP N RGD:5509061 20240509 MGI PMID:37589122 735370 Calm1 calmodulin 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20190711 MGI PMID:30322141 735370 Calm1 calmodulin 1 gene MP:0004085 abnormal heartbeat IAGP N RGD:5509061 20240509 MGI PMID:37589122 735370 Calm1 calmodulin 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20240509 MGI PMID:37589122 735370 Calm1 calmodulin 1 gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20240613 MGI PMID:37589122 735370 Calm1 calmodulin 1 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20240509 MGI PMID:37589122 735370 Calm1 calmodulin 1 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20240509 MGI PMID:37589122 735370 Calm1 calmodulin 1 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20240509 MGI PMID:37589122 735370 Calm1 calmodulin 1 gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20240509 MGI PMID:37589122 735370 Calm1 calmodulin 1 gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20240509 MGI PMID:37589122 735370 Calm1 calmodulin 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20240509 MGI PMID:37589122 735370 Calm1 calmodulin 1 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20240509 MGI PMID:37589122 735370 Calm1 calmodulin 1 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20190711 MGI PMID:30322141 735372 Rnh1 ribonuclease/angiogenin inhibitor 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20190221 MGI PMID:29408805 735372 Rnh1 ribonuclease/angiogenin inhibitor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20190221 MGI PMID:29408805 735372 Rnh1 ribonuclease/angiogenin inhibitor 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20190221 MGI PMID:29408805 735372 Rnh1 ribonuclease/angiogenin inhibitor 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20190221 MGI PMID:29408805 735372 Rnh1 ribonuclease/angiogenin inhibitor 1 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20190221 MGI PMID:29408805 735372 Rnh1 ribonuclease/angiogenin inhibitor 1 gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20190221 MGI PMID:29408805 735372 Rnh1 ribonuclease/angiogenin inhibitor 1 gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20190221 MGI PMID:29408805 735372 Rnh1 ribonuclease/angiogenin inhibitor 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20190221 MGI PMID:29408805 735372 Rnh1 ribonuclease/angiogenin inhibitor 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20190221 MGI PMID:29408805 735372 Rnh1 ribonuclease/angiogenin inhibitor 1 gene MP:0011176 abnormal erythroblast morphology IAGP N RGD:5509061 20190221 MGI PMID:29408805 735372 Rnh1 ribonuclease/angiogenin inhibitor 1 gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20190221 MGI PMID:29408805 735372 Rnh1 ribonuclease/angiogenin inhibitor 1 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20190221 MGI PMID:29408805 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12441304 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18663089 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20170323 MGI PMID:26076038 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:12441304 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000399 increased curvature of guard hairs IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000400 abnormal awl hair morphology IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000401 increased curvature of awl hairs IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000405 abnormal auchene hair morphology IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15286002 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:18663089 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20170323 MGI PMID:26076038 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20141003 MGI 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:23610558 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10772805 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:10772805 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:10772805 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:12441304 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10772805 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15736264 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:15286002 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16027259 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0002582 disorganized extraembryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:10772805 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0002746 abnormal semilunar valve morphology IAGP N RGD:5509061 20141003 MGI PMID:12441304 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:16027259 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003034 increased pulmonary vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:15286002 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:15542835 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20170323 MGI PMID:26076038 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:10772805 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:12441304 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20141003 MGI PMID:15286002 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20141003 MGI PMID:16027259 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20141003 MGI PMID:18663089 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20170323 MGI PMID:26076038 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003812 abnormal hair medulla IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003875 abnormal hair follicle regression IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:10772805 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:10772805 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10772805 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15736264 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0003988 disorganized embryonic tissue IAGP N RGD:5509061 20141003 MGI PMID:10772805 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15286002 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16027259 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18663089 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0004012 increased pulmonary artery pressure IAGP N RGD:5509061 20141003 MGI PMID:15286002 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0004012 increased pulmonary artery pressure IAGP N RGD:5509061 20141003 MGI PMID:18663089 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0004056 abnormal myocardium compact layer morphology IEA N RGD:5509061 20141003 MGI 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:12441304 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0005072 abnormal hair follicle melanin granule morphology IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10772805 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0006134 artery occlusion IAGP N RGD:5509061 20141003 MGI PMID:18663089 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:15542835 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0008732 reduced hair shaft melanin granule number IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0008733 abnormal hair shaft melanin granule distribution IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0008767 abnormal hair medullary septa cells IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0009002 premature hair regrowth IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0009351 thin hair shaft IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0009659 striated fur IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0009798 abnormal ophthalmic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:24052814 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:23610558 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0010389 mosaic coat color IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20141003 MGI 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0010684 abnormal hair follicle outer root sheath morphology IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0010758 increased right ventricle systolic pressure IAGP N RGD:5509061 20170323 MGI PMID:26076038 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16027259 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15736264 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10772805 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12441304 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16027259 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23610558 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0011105 embryonic lethality between implantation and placentation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24116187 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0011139 increased lung endothelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18663089 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20170323 MGI PMID:26076038 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0011661 persistent truncus arteriosus type i IEA N RGD:5509061 20141003 MGI 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0011664 persistent truncus arteriosus type iv IEA N RGD:5509061 20141003 MGI 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0012401 long nails IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0030574 increased hair follicle cell proliferation IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0030918 small melanosome IAGP N RGD:5509061 20181227 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0030919 absent hair follicle bulb IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0030922 absent hair club IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0030924 early exit from telogen phase IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0030925 early exit from anagen phase IAGP N RGD:5509061 20181220 MGI PMID:22611050 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0031167 abnormal lung thrombosis IAGP N RGD:5509061 20201210 MGI PMID:18663089 735374 Bmpr2 bone morphogenetic protein receptor type 2 gene MP:0031510 increased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:18663089 735376 Cdh8 cadherin 8 gene MP:0001391 abnormal tail movements IAGP N RGD:5509061 20141003 MGI PMID:17392463 735376 Cdh8 cadherin 8 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17392463 735376 Cdh8 cadherin 8 gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20141003 MGI PMID:17392463 735376 Cdh8 cadherin 8 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17392463 735376 Cdh8 cadherin 8 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20180412 MGI PMID:25126785 735377 Stk3 serine/threonine kinase 3 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:19878874 735377 Stk3 serine/threonine kinase 3 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:20080689 735377 Stk3 serine/threonine kinase 3 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20080689 735377 Stk3 serine/threonine kinase 3 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0000745 tremors IEA N RGD:5509061 20181227 MGI 735377 Stk3 serine/threonine kinase 3 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:19878874 735377 Stk3 serine/threonine kinase 3 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:23620511 735377 Stk3 serine/threonine kinase 3 gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 735377 Stk3 serine/threonine kinase 3 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19878874 735377 Stk3 serine/threonine kinase 3 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:19878874 735377 Stk3 serine/threonine kinase 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23620511 735377 Stk3 serine/threonine kinase 3 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:23620511 735377 Stk3 serine/threonine kinase 3 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23620511 735377 Stk3 serine/threonine kinase 3 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:23620511 735377 Stk3 serine/threonine kinase 3 gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:20080689 735377 Stk3 serine/threonine kinase 3 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19878874 735377 Stk3 serine/threonine kinase 3 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19878874 735377 Stk3 serine/threonine kinase 3 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20080689 735377 Stk3 serine/threonine kinase 3 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20170223 MGI PMID:26131558 735377 Stk3 serine/threonine kinase 3 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20080689 735377 Stk3 serine/threonine kinase 3 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19878874 735377 Stk3 serine/threonine kinase 3 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:20080689 735377 Stk3 serine/threonine kinase 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19878874 735377 Stk3 serine/threonine kinase 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:19878874 735377 Stk3 serine/threonine kinase 3 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0004265 abnormal placental transport IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0005141 liver hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19878874 735377 Stk3 serine/threonine kinase 3 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:19878874 735377 Stk3 serine/threonine kinase 3 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 735377 Stk3 serine/threonine kinase 3 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20080689 735377 Stk3 serine/threonine kinase 3 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0008891 decreased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20141003 MGI PMID:19878874 735377 Stk3 serine/threonine kinase 3 gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20141003 MGI PMID:20080689 735377 Stk3 serine/threonine kinase 3 gene MP:0009658 increased placenta apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19878874 735377 Stk3 serine/threonine kinase 3 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:23620511 735377 Stk3 serine/threonine kinase 3 gene MP:0011018 pulmonary hyaline membrane formation IAGP N RGD:5509061 20141003 MGI PMID:23620511 735377 Stk3 serine/threonine kinase 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19786569 735377 Stk3 serine/threonine kinase 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19878874 735377 Stk3 serine/threonine kinase 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0011139 increased lung endothelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23620511 735377 Stk3 serine/threonine kinase 3 gene MP:0013502 decreased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:20080598 735377 Stk3 serine/threonine kinase 3 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:19786569 735378 Nrcam neuronal cell adhesion molecule gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20170420 MGI PMID:28355569 735378 Nrcam neuronal cell adhesion molecule gene MP:0000745 tremors IAGP N RGD:5509061 20170420 MGI PMID:28355569 735378 Nrcam neuronal cell adhesion molecule gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:20188654 735378 Nrcam neuronal cell adhesion molecule gene MP:0000753 paralysis IAGP N RGD:5509061 20170420 MGI PMID:28355569 735378 Nrcam neuronal cell adhesion molecule gene MP:0000754 paresis IAGP N RGD:5509061 20141003 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:11564762 735378 Nrcam neuronal cell adhesion molecule gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:11564762 735378 Nrcam neuronal cell adhesion molecule gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:11564762 735378 Nrcam neuronal cell adhesion molecule gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11564762 735378 Nrcam neuronal cell adhesion molecule gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11564762 735378 Nrcam neuronal cell adhesion molecule gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20170420 MGI PMID:28355569 735378 Nrcam neuronal cell adhesion molecule gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0000947 convulsive seizures IEA N RGD:5509061 20211021 MGI 735378 Nrcam neuronal cell adhesion molecule gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20170420 MGI PMID:28355569 735378 Nrcam neuronal cell adhesion molecule gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20170420 MGI PMID:28355569 735378 Nrcam neuronal cell adhesion molecule gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11449000 735378 Nrcam neuronal cell adhesion molecule gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11564762 735378 Nrcam neuronal cell adhesion molecule gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:19540269 735378 Nrcam neuronal cell adhesion molecule gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20188654 735378 Nrcam neuronal cell adhesion molecule gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11449000 735378 Nrcam neuronal cell adhesion molecule gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170420 MGI PMID:28355569 735378 Nrcam neuronal cell adhesion molecule gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19540269 735378 Nrcam neuronal cell adhesion molecule gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:19540269 735378 Nrcam neuronal cell adhesion molecule gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11564762 735378 Nrcam neuronal cell adhesion molecule gene MP:0002083 premature death IAGP N RGD:5509061 20170420 MGI PMID:28355569 735378 Nrcam neuronal cell adhesion molecule gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20170420 MGI PMID:28355569 735378 Nrcam neuronal cell adhesion molecule gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0002579 disorganized secondary lens fibers IAGP N RGD:5509061 20141003 MGI PMID:11449000 735378 Nrcam neuronal cell adhesion molecule gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:19540269 735378 Nrcam neuronal cell adhesion molecule gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:19540269 735378 Nrcam neuronal cell adhesion molecule gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:19540269 735378 Nrcam neuronal cell adhesion molecule gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11564762 735378 Nrcam neuronal cell adhesion molecule gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20170420 MGI PMID:28355569 735378 Nrcam neuronal cell adhesion molecule gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:20188654 735378 Nrcam neuronal cell adhesion molecule gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20170420 MGI PMID:28355569 735378 Nrcam neuronal cell adhesion molecule gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:11564762 735378 Nrcam neuronal cell adhesion molecule gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:20188654 735378 Nrcam neuronal cell adhesion molecule gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20170420 MGI PMID:28355569 735378 Nrcam neuronal cell adhesion molecule gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:19540269 735378 Nrcam neuronal cell adhesion molecule gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:11449000 735378 Nrcam neuronal cell adhesion molecule gene MP:0010559 heart block IAGP N RGD:5509061 20170420 MGI PMID:28355569 735378 Nrcam neuronal cell adhesion molecule gene MP:0010732 abnormal node of Ranvier morphology IAGP N RGD:5509061 20170420 MGI PMID:28355569 735378 Nrcam neuronal cell adhesion molecule gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20188654 735378 Nrcam neuronal cell adhesion molecule gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11564762 735378 Nrcam neuronal cell adhesion molecule gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20170105 MGI 735378 Nrcam neuronal cell adhesion molecule gene MP:0030863 decreased joint mobility IAGP N RGD:5509061 20181101 MGI PMID:19793967 735378 Nrcam neuronal cell adhesion molecule gene MP:0031203 forelimb paresis IAGP N RGD:5509061 20210218 MGI PMID:19793967 735380 Amelx amelogenin, X-linked gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0000126 brittle teeth IAGP N RGD:5509061 20141003 MGI PMID:11406633 735380 Amelx amelogenin, X-linked gene MP:0000126 brittle teeth IAGP N RGD:5509061 20141003 MGI PMID:16707492 735380 Amelx amelogenin, X-linked gene MP:0000126 brittle teeth IAGP N RGD:5509061 20141003 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0000692 small spleen IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 735380 Amelx amelogenin, X-linked gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0001157 small seminal vesicle IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0001262 decreased body weight IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17384027 735380 Amelx amelogenin, X-linked gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:11406633 735380 Amelx amelogenin, X-linked gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 735380 Amelx amelogenin, X-linked gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:12958690 735380 Amelx amelogenin, X-linked gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:16707492 735380 Amelx amelogenin, X-linked gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:17384027 735380 Amelx amelogenin, X-linked gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20141003 MGI PMID:11406633 735380 Amelx amelogenin, X-linked gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20141003 MGI PMID:12958690 735380 Amelx amelogenin, X-linked gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20141003 MGI PMID:16707492 735380 Amelx amelogenin, X-linked gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20141003 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0002649 abnormal enamel rod pattern IAGP N RGD:5509061 20141003 MGI PMID:11406633 735380 Amelx amelogenin, X-linked gene MP:0002649 abnormal enamel rod pattern IAGP N RGD:5509061 20141003 MGI PMID:12958690 735380 Amelx amelogenin, X-linked gene MP:0002649 abnormal enamel rod pattern IAGP N RGD:5509061 20141003 MGI PMID:16707492 735380 Amelx amelogenin, X-linked gene MP:0002649 abnormal enamel rod pattern IAGP N RGD:5509061 20141003 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:16707492 735380 Amelx amelogenin, X-linked gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20220519 MGI 735380 Amelx amelogenin, X-linked gene MP:0003036 vertebral transformation IEA N RGD:5509061 20230601 MGI 735380 Amelx amelogenin, X-linked gene MP:0003883 enlarged stomach IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0003932 abnormal molar crown morphology IAGP N RGD:5509061 20141003 MGI PMID:16707492 735380 Amelx amelogenin, X-linked gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20230601 MGI 735380 Amelx amelogenin, X-linked gene MP:0004830 short incisors IAGP N RGD:5509061 20141003 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20230601 MGI 735380 Amelx amelogenin, X-linked gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20230601 MGI 735380 Amelx amelogenin, X-linked gene MP:0005270 abnormal zygomatic bone morphology IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0010096 abnormal incisor color IAGP N RGD:5509061 20141003 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0011047 increased lung tissue damping IEA N RGD:5509061 20211021 MGI 735380 Amelx amelogenin, X-linked gene MP:0013129 abnormal tooth color IEA N RGD:5509061 20210826 MGI 735380 Amelx amelogenin, X-linked gene MP:0030050 large mandible IAGP N RGD:5509061 20171012 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0030089 short lower incisors IAGP N RGD:5509061 20170928 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0030090 short upper incisors IAGP N RGD:5509061 20170928 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0030450 abnormal enamel mineralization IAGP N RGD:5509061 20171221 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20171221 MGI PMID:16707492 735380 Amelx amelogenin, X-linked gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20180125 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0030458 abnormal tooth wear IAGP N RGD:5509061 20171221 MGI PMID:16707492 735380 Amelx amelogenin, X-linked gene MP:0030458 abnormal tooth wear IAGP N RGD:5509061 20180125 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0030460 enamel pits IAGP N RGD:5509061 20171221 MGI PMID:20067920 735380 Amelx amelogenin, X-linked gene MP:0030513 short Tomes' process IAGP N RGD:5509061 20180111 MGI PMID:16707492 735380 Amelx amelogenin, X-linked gene MP:0030610 absent teeth IEA N RGD:5509061 20210826 MGI 735381 Afm afamin gene MP:0000565 oligodactyly IEA N RGD:5509061 20160804 MGI 735381 Afm afamin gene MP:0003062 abnormal coping response IEA N RGD:5509061 20141003 MGI 735381 Afm afamin gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160804 MGI 735383 Tapbp TAP binding protein gene MP:0001836 abnormal antigen presentation via MHC class I IAGP N RGD:5509061 20141003 MGI PMID:10973281 735383 Tapbp TAP binding protein gene MP:0001836 abnormal antigen presentation via MHC class I IAGP N RGD:5509061 20141003 MGI PMID:10981964 735383 Tapbp TAP binding protein gene MP:0001837 defective assembly of class I molecules IAGP N RGD:5509061 20141003 MGI PMID:10981964 735383 Tapbp TAP binding protein gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:10973281 735383 Tapbp TAP binding protein gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:10981964 735383 Tapbp TAP binding protein gene MP:0002432 abnormal CD4-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10981964 735383 Tapbp TAP binding protein gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:10973281 735383 Tapbp TAP binding protein gene MP:0003945 abnormal lymphocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:16505142 735383 Tapbp TAP binding protein gene MP:0004918 abnormal negative T cell selection IAGP N RGD:5509061 20141003 MGI PMID:10981964 735383 Tapbp TAP binding protein gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:10981964 735383 Tapbp TAP binding protein gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10981964 735383 Tapbp TAP binding protein gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:10973281 735383 Tapbp TAP binding protein gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10981964 735383 Tapbp TAP binding protein gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:10973281 735383 Tapbp TAP binding protein gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10981964 735383 Tapbp TAP binding protein gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10973281 735385 Lypla1 lysophospholipase 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20210415 MGI PMID:32233916 735385 Lypla1 lysophospholipase 1 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20210415 MGI PMID:32233916 735385 Lypla1 lysophospholipase 1 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20210415 MGI PMID:32233916 735385 Lypla1 lysophospholipase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210826 MGI 735385 Lypla1 lysophospholipase 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 735385 Lypla1 lysophospholipase 1 gene MP:0020317 abnormal vascular endothelial cell adhesion IAGP N RGD:5509061 20210415 MGI PMID:32233916 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141106 MGI PMID:23129651 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0002833 increased heart weight IAGP N RGD:5509061 20170622 MGI PMID:27626666 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20170622 MGI PMID:27626666 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20170622 MGI PMID:27626666 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141106 MGI PMID:18276892 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20170622 MGI PMID:27626666 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141106 MGI PMID:20674568 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141106 MGI PMID:23129651 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141106 MGI PMID:23129651 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141106 MGI PMID:23129651 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20170622 MGI PMID:27626666 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0006038 increased mitochondrial fission IAGP N RGD:5509061 20141106 MGI PMID:23129651 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20170622 MGI PMID:27626666 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141106 MGI PMID:23129651 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141106 MGI PMID:23129651 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141106 MGI PMID:23129651 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20170622 MGI PMID:27626666 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141106 MGI PMID:18276892 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141106 MGI PMID:20674568 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20141106 MGI PMID:23129651 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20141106 MGI PMID:23129651 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20141106 MGI PMID:23129651 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0012552 lactic acidosis IAGP N RGD:5509061 20170921 MGI PMID:20674568 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0013272 abnormal translation IAGP N RGD:5509061 20170622 MGI PMID:27626666 735386 mt-Nd6 NADH dehydrogenase 6, mitochondrial gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20170622 MGI PMID:27626666 735388 Fut2 fucosyltransferase 2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:14967068 735388 Fut2 fucosyltransferase 2 gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:14967068 735388 Fut2 fucosyltransferase 2 gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:15213174 735388 Fut2 fucosyltransferase 2 gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:11713270 735388 Fut2 fucosyltransferase 2 gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:15213174 735394 Nme1 NME/NM23 nucleoside diphosphate kinase 1 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:12848338 735394 Nme1 NME/NM23 nucleoside diphosphate kinase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12848338 735394 Nme1 NME/NM23 nucleoside diphosphate kinase 1 gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:12848338 735394 Nme1 NME/NM23 nucleoside diphosphate kinase 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:12848338 735394 Nme1 NME/NM23 nucleoside diphosphate kinase 1 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:12848338 735394 Nme1 NME/NM23 nucleoside diphosphate kinase 1 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:12848338 735394 Nme1 NME/NM23 nucleoside diphosphate kinase 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12848338 735394 Nme1 NME/NM23 nucleoside diphosphate kinase 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12848338 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:1952599 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:1952599 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:1952599 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:13130470 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20201022 MGI 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20210520 MGI 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:13130470 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20201022 MGI 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0004397 absent cochlear inner hair cells IAGP N RGD:5509061 20141003 MGI PMID:1952599 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0004403 absent cochlear outer hair cells IAGP N RGD:5509061 20141003 MGI PMID:1952599 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0006429 abnormal hyaline cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0006432 abnormal costal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0008069 abnormal joint mobility IAGP N RGD:5509061 20141003 MGI PMID:13130470 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0008736 micromelia IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20220519 MGI 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:1952599 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0030026 small Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:4100752 735397 Col11a1 collagen, type XI, alpha 1 gene MP:0030837 abnormal knee joint morphology IAGP N RGD:5509061 20181025 MGI PMID:13130470 735401 Cdk6 cyclin dependent kinase 6 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:17700700 735401 Cdk6 cyclin dependent kinase 6 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17700700 735401 Cdk6 cyclin dependent kinase 6 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17700700 735401 Cdk6 cyclin dependent kinase 6 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19155308 735401 Cdk6 cyclin dependent kinase 6 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20181227 MGI 735401 Cdk6 cyclin dependent kinase 6 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17700700 735401 Cdk6 cyclin dependent kinase 6 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19155308 735401 Cdk6 cyclin dependent kinase 6 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19155308 735401 Cdk6 cyclin dependent kinase 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20609353 735401 Cdk6 cyclin dependent kinase 6 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20181227 MGI 735401 Cdk6 cyclin dependent kinase 6 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19155308 735401 Cdk6 cyclin dependent kinase 6 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19155308 735401 Cdk6 cyclin dependent kinase 6 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:19155308 735401 Cdk6 cyclin dependent kinase 6 gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:19155308 735401 Cdk6 cyclin dependent kinase 6 gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:17700700 735401 Cdk6 cyclin dependent kinase 6 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:19155308 735401 Cdk6 cyclin dependent kinase 6 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19155308 735401 Cdk6 cyclin dependent kinase 6 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20231207 MGI 735401 Cdk6 cyclin dependent kinase 6 gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17700700 735401 Cdk6 cyclin dependent kinase 6 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19155308 735401 Cdk6 cyclin dependent kinase 6 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20609353 735401 Cdk6 cyclin dependent kinase 6 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19155308 735401 Cdk6 cyclin dependent kinase 6 gene MP:0010129 increased DN1 thymic pro-T cell number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0010130 decreased DN1 thymic pro-T cell number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0010132 decreased DN2 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0010133 increased DN3 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0010136 decreased DN4 thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20609353 735401 Cdk6 cyclin dependent kinase 6 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21508411 735401 Cdk6 cyclin dependent kinase 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17700700 735401 Cdk6 cyclin dependent kinase 6 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17700700 735401 Cdk6 cyclin dependent kinase 6 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0013585 thymus cortex atrophy IAGP N RGD:5509061 20150319 MGI PMID:15315761 735401 Cdk6 cyclin dependent kinase 6 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:19155308 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20211021 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20160421 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160421 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20211021 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000256 echinocytosis IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000274 enlarged heart IEA N RGD:5509061 20160811 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000314 schistocytosis IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20160811 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20181227 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000709 enlarged thymus IEA N RGD:5509061 20181227 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21896769 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000888 absent cerebellar granule layer IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200514 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0001148 enlarged testis IEA N RGD:5509061 20200514 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19892703 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0001293 anophthalmia IEA N RGD:5509061 20160811 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20200402 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0001304 cataract IEA N RGD:5509061 20200402 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21896769 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:19892703 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20171228 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20160421 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002626 increased heart rate IEA N RGD:5509061 20200514 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002642 anisocytosis IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19892703 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002813 microcytosis IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002833 increased heart weight IEA N RGD:5509061 20200402 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19892703 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:21896769 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20220811 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0003918 decreased kidney weight IEA N RGD:5509061 20201022 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20240523 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20190502 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20160421 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20141003 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20141003 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21896769 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20160421 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:21896769 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19892703 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19892703 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20171228 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0006353 increased glycosylated hemoglobin level IEA N RGD:5509061 20210128 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20201231 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:19892703 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20161201 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19892703 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19892703 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0009454 impaired contextual conditioning behavior IEA N RGD:5509061 20231207 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0010074 stomatocytosis IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19892703 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0010093 decreased circulating magnesium level IEA N RGD:5509061 20160804 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20200402 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0010177 acanthocytosis IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0010507 shortened RR interval IEA N RGD:5509061 20160421 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0010895 increased lung compliance IEA N RGD:5509061 20210520 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0011045 decreased lung elastance IEA N RGD:5509061 20211021 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20160421 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21896769 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0011913 abnormal reticulocyte cell number IAGP N RGD:5509061 20170216 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:19892703 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20181227 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:21896769 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0013418 increased memory-marker gamma-delta T cell number IEA N RGD:5509061 20201231 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0013514 increased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0013675 decreased Ly6C-positive mature NK cell number IEA N RGD:5509061 20211021 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0013873 abnormal ductus venosus morphology IEA N RGD:5509061 20171228 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:19217427 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20231207 MGI 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0030022 decreased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:21896769 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0031084 decreased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:27666489 735403 Prkab1 protein kinase, AMP-activated, beta 1 non-catalytic subunit gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:19892703 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17128269 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0000692 small spleen IEA N RGD:5509061 20210826 MGI 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20210826 MGI 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0000709 enlarged thymus IEA N RGD:5509061 20210826 MGI 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11069976 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11069976 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:11069976 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11108293 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11108293 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11108293 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10932193 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001148 enlarged testis IEA N RGD:5509061 20210826 MGI 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:10932193 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10932193 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10932193 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20209163 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20209163 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11069976 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11069976 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11069976 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:10964952 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:11069976 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:11108293 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11108293 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10932193 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:10932193 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10932193 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11108293 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:16630062 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:16982426 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11108293 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20210826 MGI 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10932193 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:11108293 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11486043 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10932193 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:11069976 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:10964952 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0002915 abnormal synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:11069976 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16630062 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:17128269 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:10964952 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10932193 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10932193 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:20209163 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20240523 MGI 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17128269 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10932193 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:10932193 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:17128269 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:10964952 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:11108293 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10932193 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:10932193 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20141003 MGI PMID:11108293 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:20209163 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:20209163 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:16630062 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:19001277 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:17128269 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:11069976 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:11069976 735406 Camk4 calcium/calmodulin-dependent protein kinase IV gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:10964952 735408 mt-Atp8 ATP synthase 8, mitochondrial gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141106 MGI PMID:19037013 735409 Asic1 acid-sensing ion channel 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11988176 735409 Asic1 acid-sensing ion channel 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20201022 MGI 735409 Asic1 acid-sensing ion channel 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20231207 MGI 735409 Asic1 acid-sensing ion channel 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:23365222 735409 Asic1 acid-sensing ion channel 1 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11988176 735409 Asic1 acid-sensing ion channel 1 gene MP:0002807 abnormal eye blink conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11988176 735409 Asic1 acid-sensing ion channel 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:11988176 735409 Asic1 acid-sensing ion channel 1 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:11988176 735409 Asic1 acid-sensing ion channel 1 gene MP:0009244 abnormal acid-activated cation-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:11988176 735412 Cds2 CDP-diacylglycerol synthase 2 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 735412 Cds2 CDP-diacylglycerol synthase 2 gene MP:0003889 enhanced sensorimotor gating IEA N RGD:5509061 20111116 MGI 735412 Cds2 CDP-diacylglycerol synthase 2 gene MP:0005015 increased T cell number IEA N RGD:5509061 20111116 MGI 735412 Cds2 CDP-diacylglycerol synthase 2 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20111116 MGI 735412 Cds2 CDP-diacylglycerol synthase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 735416 Tfec transcription factor EC gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:11930005 735416 Tfec transcription factor EC gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11930005 735416 Tfec transcription factor EC gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20230601 MGI 735416 Tfec transcription factor EC gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20230601 MGI 735416 Tfec transcription factor EC gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11930005 735416 Tfec transcription factor EC gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11930005 735416 Tfec transcription factor EC gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210826 MGI 735417 Cfl1 cofilin 1, non-muscle gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17875668 735417 Cfl1 cofilin 1, non-muscle gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:15649475 735417 Cfl1 cofilin 1, non-muscle gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:15649475 735417 Cfl1 cofilin 1, non-muscle gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17875668 735417 Cfl1 cofilin 1, non-muscle gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:20472933 735417 Cfl1 cofilin 1, non-muscle gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:15649475 735417 Cfl1 cofilin 1, non-muscle gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15649475 735417 Cfl1 cofilin 1, non-muscle gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17875668 735417 Cfl1 cofilin 1, non-muscle gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:17875668 735417 Cfl1 cofilin 1, non-muscle gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17875668 735417 Cfl1 cofilin 1, non-muscle gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20472933 735417 Cfl1 cofilin 1, non-muscle gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15649475 735417 Cfl1 cofilin 1, non-muscle gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17875668 735417 Cfl1 cofilin 1, non-muscle gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:15649475 735417 Cfl1 cofilin 1, non-muscle gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:20472933 735417 Cfl1 cofilin 1, non-muscle gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:17875668 735417 Cfl1 cofilin 1, non-muscle gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:17875668 735417 Cfl1 cofilin 1, non-muscle gene MP:0004066 abnormal primitive node morphology IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:17875668 735417 Cfl1 cofilin 1, non-muscle gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:20472933 735417 Cfl1 cofilin 1, non-muscle gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0005324 ascites IAGP N RGD:5509061 20141003 MGI PMID:20472933 735417 Cfl1 cofilin 1, non-muscle gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:20472933 735417 Cfl1 cofilin 1, non-muscle gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:15649475 735417 Cfl1 cofilin 1, non-muscle gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:20472933 735417 Cfl1 cofilin 1, non-muscle gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:17875668 735417 Cfl1 cofilin 1, non-muscle gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17875668 735417 Cfl1 cofilin 1, non-muscle gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17875668 735417 Cfl1 cofilin 1, non-muscle gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15649475 735417 Cfl1 cofilin 1, non-muscle gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 735417 Cfl1 cofilin 1, non-muscle gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:17875668 735417 Cfl1 cofilin 1, non-muscle gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20230323 MGI PMID:33845164 735417 Cfl1 cofilin 1, non-muscle gene MP:0011868 podocyte microvillus transformation IAGP N RGD:5509061 20141003 MGI PMID:20472933 735417 Cfl1 cofilin 1, non-muscle gene MP:0012027 abnormal embryonic cilium location or orientation IAGP N RGD:5509061 20141003 MGI PMID:23406901 735417 Cfl1 cofilin 1, non-muscle gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:15649475 735417 Cfl1 cofilin 1, non-muscle gene MP:0012706 decreased embryonic neuroepithelial cell proliferation IAGP N RGD:5509061 20190704 MGI PMID:15649475 735417 Cfl1 cofilin 1, non-muscle gene MP:0012728 abnormal somite border morphology IAGP N RGD:5509061 20141003 MGI PMID:15649475 735417 Cfl1 cofilin 1, non-muscle gene MP:0012746 abnormal neural crest cell delamination IAGP N RGD:5509061 20141003 MGI PMID:15649475 735417 Cfl1 cofilin 1, non-muscle gene MP:0013198 absent head mesenchyme IAGP N RGD:5509061 20190704 MGI PMID:15649475 735419 Trpv6 transient receptor potential cation channel, subfamily V, member 6 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:21540454 735419 Trpv6 transient receptor potential cation channel, subfamily V, member 6 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:21540454 735419 Trpv6 transient receptor potential cation channel, subfamily V, member 6 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21540454 735419 Trpv6 transient receptor potential cation channel, subfamily V, member 6 gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21540454 735419 Trpv6 transient receptor potential cation channel, subfamily V, member 6 gene MP:0009325 necrospermia IAGP N RGD:5509061 20141003 MGI PMID:21540454 735419 Trpv6 transient receptor potential cation channel, subfamily V, member 6 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:21540454 735420 Unc13c unc-13 homolog C gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210826 MGI 735420 Unc13c unc-13 homolog C gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11150314 735420 Unc13c unc-13 homolog C gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:11150314 735420 Unc13c unc-13 homolog C gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:11150314 735420 Unc13c unc-13 homolog C gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 735422 Hpca hippocalcin gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:15607944 735422 Hpca hippocalcin gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201022 MGI 735422 Hpca hippocalcin gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 735422 Hpca hippocalcin gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 735422 Hpca hippocalcin gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:15607944 735422 Hpca hippocalcin gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 735422 Hpca hippocalcin gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:15607944 735422 Hpca hippocalcin gene MP:0010052 increased grip strength IEA N RGD:5509061 20220519 MGI 735422 Hpca hippocalcin gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20221215 MGI 735427 Cish cytokine inducible SH2-containing protein gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0002281 abnormal respiratory mucosa goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0008672 increased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:23727894 735427 Cish cytokine inducible SH2-containing protein gene MP:0008711 increased interleukin-9 secretion IAGP N RGD:5509061 20141003 MGI PMID:23727894 735429 Insig2 insulin induced gene 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16100574 735429 Insig2 insulin induced gene 2 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:16100574 735429 Insig2 insulin induced gene 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16100574 735429 Insig2 insulin induced gene 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16100574 735429 Insig2 insulin induced gene 2 gene MP:0002139 abnormal hepatobiliary system physiology IAGP N RGD:5509061 20141003 MGI PMID:16100574 735429 Insig2 insulin induced gene 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16100574 735429 Insig2 insulin induced gene 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16100574 735429 Insig2 insulin induced gene 2 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16100574 735429 Insig2 insulin induced gene 2 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16100574 735429 Insig2 insulin induced gene 2 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 735429 Insig2 insulin induced gene 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:16100574 735429 Insig2 insulin induced gene 2 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16100574 735431 Il1r1 interleukin 1 receptor, type I gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23219391 735431 Il1r1 interleukin 1 receptor, type I gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23064362 735431 Il1r1 interleukin 1 receptor, type I gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23219391 735431 Il1r1 interleukin 1 receptor, type I gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:19347044 735431 Il1r1 interleukin 1 receptor, type I gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20231207 MGI 735431 Il1r1 interleukin 1 receptor, type I gene MP:0000274 enlarged heart IEA N RGD:5509061 20231207 MGI 735431 Il1r1 interleukin 1 receptor, type I gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:14693705 735431 Il1r1 interleukin 1 receptor, type I gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20231207 MGI 735431 Il1r1 interleukin 1 receptor, type I gene MP:0000691 enlarged spleen IEA N RGD:5509061 20231207 MGI 735431 Il1r1 interleukin 1 receptor, type I gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11122355 735431 Il1r1 interleukin 1 receptor, type I gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11994477 735431 Il1r1 interleukin 1 receptor, type I gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:20696775 735431 Il1r1 interleukin 1 receptor, type I gene MP:0001337 dry eyes IAGP N RGD:5509061 20141003 MGI PMID:20696775 735431 Il1r1 interleukin 1 receptor, type I gene MP:0001346 abnormal lacrimal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:20696775 735431 Il1r1 interleukin 1 receptor, type I gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19429130 735431 Il1r1 interleukin 1 receptor, type I gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:18329246 735431 Il1r1 interleukin 1 receptor, type I gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20150521 MGI PMID:25698726 735431 Il1r1 interleukin 1 receptor, type I gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:11238652 735431 Il1r1 interleukin 1 receptor, type I gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20141003 MGI PMID:11238652 735431 Il1r1 interleukin 1 receptor, type I gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:17908936 735431 Il1r1 interleukin 1 receptor, type I gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20231207 MGI 735431 Il1r1 interleukin 1 receptor, type I gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150521 MGI PMID:25698726 735431 Il1r1 interleukin 1 receptor, type I gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19100239 735431 Il1r1 interleukin 1 receptor, type I gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10595943 735431 Il1r1 interleukin 1 receptor, type I gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11994477 735431 Il1r1 interleukin 1 receptor, type I gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9278338 735431 Il1r1 interleukin 1 receptor, type I gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12672065 735431 Il1r1 interleukin 1 receptor, type I gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16886064 735431 Il1r1 interleukin 1 receptor, type I gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:9555664 735431 Il1r1 interleukin 1 receptor, type I gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:19389930 735431 Il1r1 interleukin 1 receptor, type I gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19347044 735431 Il1r1 interleukin 1 receptor, type I gene MP:0002865 increased growth rate IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:19347044 735431 Il1r1 interleukin 1 receptor, type I gene MP:0003053 delayed tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:10946764 735431 Il1r1 interleukin 1 receptor, type I gene MP:0003068 enlarged kidney IEA N RGD:5509061 20231207 MGI 735431 Il1r1 interleukin 1 receptor, type I gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:23219391 735431 Il1r1 interleukin 1 receptor, type I gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:12133972 735431 Il1r1 interleukin 1 receptor, type I gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:11122355 735431 Il1r1 interleukin 1 receptor, type I gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:11994477 735431 Il1r1 interleukin 1 receptor, type I gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20230831 MGI PMID:37315560 735431 Il1r1 interleukin 1 receptor, type I gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20141003 MGI PMID:9278338 735431 Il1r1 interleukin 1 receptor, type I gene MP:0003917 increased kidney weight IEA N RGD:5509061 20240523 MGI 735431 Il1r1 interleukin 1 receptor, type I gene MP:0003959 abnormal lean body mass IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:9555664 735431 Il1r1 interleukin 1 receptor, type I gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:23090995 735431 Il1r1 interleukin 1 receptor, type I gene MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20200130 MGI PMID:30662948 735431 Il1r1 interleukin 1 receptor, type I gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:14693705 735431 Il1r1 interleukin 1 receptor, type I gene MP:0004822 decreased susceptibility to experimental autoimmune uveoretinitis IAGP N RGD:5509061 20141003 MGI PMID:10509653 735431 Il1r1 interleukin 1 receptor, type I gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:16565512 735431 Il1r1 interleukin 1 receptor, type I gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:19501000 735431 Il1r1 interleukin 1 receptor, type I gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:10595943 735431 Il1r1 interleukin 1 receptor, type I gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:18329246 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12672065 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:23219391 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23219391 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12672065 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:11994477 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12672065 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005190 osteomyelitis IAGP N RGD:5509061 20141003 MGI PMID:10595943 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:19347044 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:23219391 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:9555664 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:9555664 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:19347044 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:9278338 735431 Il1r1 interleukin 1 receptor, type I gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20696775 735431 Il1r1 interleukin 1 receptor, type I gene MP:0006087 increased body mass index IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0006194 keratoconjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:20696775 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008087 decreased T helper 1 cell number IAGP N RGD:5509061 20200130 MGI PMID:30662948 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20200130 MGI PMID:30662948 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20230831 MGI PMID:37315560 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:11994477 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20230831 MGI PMID:37315560 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:11994477 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:19347044 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:9278338 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:9317135 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008635 increased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:11994477 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008636 decreased circulating interleukin-18 level IAGP N RGD:5509061 20141003 MGI PMID:11994477 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:11994477 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:21600797 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:10509653 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:11994477 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:19389930 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:9278338 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:11238652 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:16407889 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:11238652 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:9317135 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008838 decreased transforming growth factor beta level IAGP N RGD:5509061 20141003 MGI PMID:19389930 735431 Il1r1 interleukin 1 receptor, type I gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:20696775 735431 Il1r1 interleukin 1 receptor, type I gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19429130 735431 Il1r1 interleukin 1 receptor, type I gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23219391 735431 Il1r1 interleukin 1 receptor, type I gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11994477 735431 Il1r1 interleukin 1 receptor, type I gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20200130 MGI PMID:30662948 735431 Il1r1 interleukin 1 receptor, type I gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0010762 abnormal microglial cell activation IAGP N RGD:5509061 20150521 MGI PMID:25698726 735431 Il1r1 interleukin 1 receptor, type I gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18329246 735431 Il1r1 interleukin 1 receptor, type I gene MP:0012164 abnormal conjunctiva goblet cell morphology IAGP N RGD:5509061 20141204 MGI PMID:20696775 735431 Il1r1 interleukin 1 receptor, type I gene MP:0013251 dental pulp necrosis IAGP N RGD:5509061 20141003 MGI PMID:10595943 735431 Il1r1 interleukin 1 receptor, type I gene MP:0013754 abnormal ocular surface morphology IAGP N RGD:5509061 20150416 MGI PMID:20696775 735431 Il1r1 interleukin 1 receptor, type I gene MP:0014441 decreased response to leptin IAGP N RGD:5509061 20240613 MGI PMID:16644674 735431 Il1r1 interleukin 1 receptor, type I gene MP:0020913 increased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:23219391 735431 Il1r1 interleukin 1 receptor, type I gene MP:0031233 decreased circulating serum amyloid protein level IAGP N RGD:5509061 20210225 MGI PMID:9278338 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:24318996 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20230601 MGI 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230601 MGI 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20230601 MGI 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20150219 MGI PMID:24802129 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20230601 MGI 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20150219 MGI PMID:24802129 735436 Sult1a1 sulfotransferase family 1A, phenol-preferring, member 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 735439 Nploc4 NPL4 homolog, ubiquitin recognition factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20170803 MGI PMID:26392310 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20210520 MGI 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0000745 tremors IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0000746 weakness IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0000753 paralysis IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20170803 MGI PMID:26392310 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20160421 MGI 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0002083 premature death IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20160421 MGI 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20210128 MGI 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0002900 abnormal urine phosphate level IAGP N RGD:5509061 20170803 MGI PMID:26392310 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20170803 MGI PMID:26392310 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20160304 MGI PMID:22311909 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:15178683 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20160304 MGI PMID:22311909 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20160304 MGI PMID:22311909 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20210128 MGI 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0005307 head tossing IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0005424 jerky movement IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20160304 MGI PMID:22311909 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20160304 MGI PMID:22311909 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20170803 MGI PMID:26392310 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0009849 increased vertical stereotypic behavior IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15178683 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IEA N RGD:5509061 20241017 MGI 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20170803 MGI PMID:26392310 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0011185 absent primitive endoderm IEA N RGD:5509061 20191205 MGI 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0011221 decreased intestinal calcium absorption IAGP N RGD:5509061 20170803 MGI PMID:26392310 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0011975 neuronal cytoplasmic inclusions IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0012102 absent trophectoderm IEA N RGD:5509061 20191205 MGI 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0012347 low sweet preference IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0013189 abnormal exploration in a new environment IAGP N RGD:5509061 20190307 MGI PMID:27329763 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20221103 MGI 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20170803 MGI PMID:26392310 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20170803 MGI PMID:26392310 735441 Atp2b1 ATPase, Ca++ transporting, plasma membrane 1 gene MP:0030214 muscle fasciculation IAGP N RGD:5509061 20190307 MGI PMID:27329763 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:11454706 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:15340075 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:8799128 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:9806499 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:9806499 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:11454706 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:11454706 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0001857 pericarditis IAGP N RGD:5509061 20141003 MGI PMID:11454706 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:9806499 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11454706 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11454706 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11454706 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12773568 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15340075 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:15472121 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:15472121 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11454706 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:15472121 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:11454706 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:9806499 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15472121 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9806499 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15472121 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:16936011 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:15472121 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:16936011 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15340075 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:15340075 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:11454706 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:11454706 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20141003 MGI PMID:16936011 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0008638 increased circulating interleukin-1 alpha level IAGP N RGD:5509061 20141003 MGI PMID:16936011 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11454706 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8799128 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9806499 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11454706 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0011191 increased embryonic epiblast cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9806499 735443 Apex1 apurinic/apyrimidinic endonuclease 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11454706 735444 Plcg2 phospholipase C, gamma 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17053833 735444 Plcg2 phospholipase C, gamma 2 gene MP:0000574 abnormal foot pad morphology IAGP N RGD:5509061 20141003 MGI PMID:19531496 735444 Plcg2 phospholipase C, gamma 2 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16585562 735444 Plcg2 phospholipase C, gamma 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16585562 735444 Plcg2 phospholipase C, gamma 2 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17030619 735444 Plcg2 phospholipase C, gamma 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:15845450 735444 Plcg2 phospholipase C, gamma 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16354682 735444 Plcg2 phospholipase C, gamma 2 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19056831 735444 Plcg2 phospholipase C, gamma 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20210902 MGI PMID:34254352 735444 Plcg2 phospholipase C, gamma 2 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:10925250 735444 Plcg2 phospholipase C, gamma 2 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12928432 735444 Plcg2 phospholipase C, gamma 2 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16354682 735444 Plcg2 phospholipase C, gamma 2 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:22761313 735444 Plcg2 phospholipase C, gamma 2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:19531496 735444 Plcg2 phospholipase C, gamma 2 gene MP:0001879 abnormal lymphatic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19056831 735444 Plcg2 phospholipase C, gamma 2 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17030619 735444 Plcg2 phospholipase C, gamma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17030619 735444 Plcg2 phospholipase C, gamma 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19056831 735444 Plcg2 phospholipase C, gamma 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16354682 735444 Plcg2 phospholipase C, gamma 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16585562 735444 Plcg2 phospholipase C, gamma 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17030619 735444 Plcg2 phospholipase C, gamma 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22761313 735444 Plcg2 phospholipase C, gamma 2 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20111715 735444 Plcg2 phospholipase C, gamma 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15845450 735444 Plcg2 phospholipase C, gamma 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17030619 735444 Plcg2 phospholipase C, gamma 2 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:15845450 735444 Plcg2 phospholipase C, gamma 2 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:15845450 735444 Plcg2 phospholipase C, gamma 2 gene MP:0003132 increased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:17030619 735444 Plcg2 phospholipase C, gamma 2 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:20111715 735444 Plcg2 phospholipase C, gamma 2 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:15845450 735444 Plcg2 phospholipase C, gamma 2 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17053833 735444 Plcg2 phospholipase C, gamma 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16585562 735444 Plcg2 phospholipase C, gamma 2 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:16002670 735444 Plcg2 phospholipase C, gamma 2 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:18203684 735444 Plcg2 phospholipase C, gamma 2 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10925250 735444 Plcg2 phospholipase C, gamma 2 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12446777 735444 Plcg2 phospholipase C, gamma 2 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17030619 735444 Plcg2 phospholipase C, gamma 2 gene MP:0005461 abnormal dendritic cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20111715 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:10925250 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008167 increased B-1a cell number IAGP N RGD:5509061 20141003 MGI PMID:21623346 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008168 decreased B-1a cell number IEA N RGD:5509061 20181011 MGI 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:12928432 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10925250 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16354682 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16585562 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:15845450 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008207 decreased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:15845450 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:10925250 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16354682 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10925250 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:15845450 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16354682 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008214 increased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:10925250 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16354682 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:16585562 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:17053833 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008561 decreased tumor necrosis factor secretion IEA N RGD:5509061 20150402 MGI 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16002670 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18203684 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12928432 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16354682 735444 Plcg2 phospholipase C, gamma 2 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16585562 735444 Plcg2 phospholipase C, gamma 2 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:17053833 735444 Plcg2 phospholipase C, gamma 2 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:15774906 735444 Plcg2 phospholipase C, gamma 2 gene MP:0009925 increased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12928432 735444 Plcg2 phospholipase C, gamma 2 gene MP:0010740 abnormal dendritic cell chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:20111715 735444 Plcg2 phospholipase C, gamma 2 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22683124 735444 Plcg2 phospholipase C, gamma 2 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 735444 Plcg2 phospholipase C, gamma 2 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:17053833 735444 Plcg2 phospholipase C, gamma 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16585562 735444 Plcg2 phospholipase C, gamma 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16354682 735444 Plcg2 phospholipase C, gamma 2 gene MP:0012080 chylous ascites IAGP N RGD:5509061 20141003 MGI PMID:19056831 735444 Plcg2 phospholipase C, gamma 2 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17030619 735444 Plcg2 phospholipase C, gamma 2 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 735444 Plcg2 phospholipase C, gamma 2 gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:12446777 735444 Plcg2 phospholipase C, gamma 2 gene MP:0020879 abnormal calcium level IAGP N RGD:5509061 20210902 MGI PMID:34254352 735444 Plcg2 phospholipase C, gamma 2 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:16002670 735444 Plcg2 phospholipase C, gamma 2 gene MP:0030951 abnormal endocytosis IAGP N RGD:5509061 20210902 MGI PMID:34254352 735446 Rgs1 regulator of G-protein signaling 1 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:15199133 735446 Rgs1 regulator of G-protein signaling 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15100254 735446 Rgs1 regulator of G-protein signaling 1 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15199133 735446 Rgs1 regulator of G-protein signaling 1 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:15199133 735446 Rgs1 regulator of G-protein signaling 1 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:15199133 735446 Rgs1 regulator of G-protein signaling 1 gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:15199133 735446 Rgs1 regulator of G-protein signaling 1 gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:15199133 735446 Rgs1 regulator of G-protein signaling 1 gene MP:0014471 enhanced B cell migration IAGP N RGD:5509061 20240613 MGI PMID:15199133 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161222 MGI PMID:26412491 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20161222 MGI PMID:26412491 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20161222 MGI PMID:26412491 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20160929 MGI PMID:27534441 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19116659 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:11691998 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19116659 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23385584 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20161222 MGI PMID:26412491 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20161222 MGI PMID:26412491 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20161222 MGI PMID:26412491 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:11691998 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:11691998 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:16793874 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0008504 abnormal adrenal chromaffin cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18703708 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20161222 MGI PMID:26412491 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11691998 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20161222 MGI PMID:26412491 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20161222 MGI PMID:26412491 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:16793874 735449 Vamp2 vesicle-associated membrane protein 2 gene MP:0021198 abnormal sleep duration IAGP N RGD:5509061 20220922 MGI PMID:27534441 735451 Gpx5 glutathione peroxidase 5 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 735451 Gpx5 glutathione peroxidase 5 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 735451 Gpx5 glutathione peroxidase 5 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:19546506 735451 Gpx5 glutathione peroxidase 5 gene MP:0009232 abnormal sperm nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19546506 735452 Stk10 serine/threonine kinase 10 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10692593 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:22678062 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12890513 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20170223 MGI PMID:26831068 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:10929716 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:12684182 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15357422 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:17074442 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0002626 increased heart rate IAGP N RGD:5509061 20170223 MGI PMID:26831068 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:10929716 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:12684182 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:15357422 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:16828974 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20150611 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:10929716 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20170223 MGI PMID:26831068 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0003928 increased heart rate variability IAGP N RGD:5509061 20170223 MGI PMID:26831068 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004122 abnormal sinus arrhythmia IAGP N RGD:5509061 20141003 MGI PMID:10929716 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20170223 MGI PMID:26831068 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10929716 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12684182 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10929716 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12684182 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12890513 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16828974 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10929716 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12684182 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15357422 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:17074442 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10929716 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:14645476 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16828974 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17074442 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15357422 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17074442 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004530 absent outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:15357422 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004562 abnormal inner hair cell synaptic ribbon morphology IAGP N RGD:5509061 20141003 MGI PMID:16828974 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004563 absent active-zone-anchored inner hair cell synaptic ribbon IAGP N RGD:5509061 20141003 MGI PMID:12684182 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004633 abnormal cochlear IHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12684182 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004633 abnormal cochlear IHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:14645476 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004633 abnormal cochlear IHC efferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:16828974 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004716 abnormal cochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12890513 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:17074442 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:22678062 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:15357422 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:10929716 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12684182 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004746 abnormal cochlear IHC afferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:12684182 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004746 abnormal cochlear IHC afferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:14645476 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0004746 abnormal cochlear IHC afferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:16828974 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:10929716 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20170223 MGI PMID:26831068 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:10929716 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20170223 MGI PMID:26831068 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:10929716 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:12684182 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:12890513 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:15357422 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0008543 atrial fibrillation IAGP N RGD:5509061 20170223 MGI PMID:26831068 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22678062 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0010506 prolonged RR interval IAGP N RGD:5509061 20141003 MGI PMID:10929716 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:10929716 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20170223 MGI PMID:26831068 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0010559 heart block IAGP N RGD:5509061 20170223 MGI PMID:26831068 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20170223 MGI PMID:26831068 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20150611 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:22678062 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:10929716 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11581302 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15357422 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17074442 735458 Cacna1d calcium channel, voltage-dependent, L type, alpha 1D subunit gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:22678062 735460 Idi1 isopentenyl-diphosphate delta isomerase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 735460 Idi1 isopentenyl-diphosphate delta isomerase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 735460 Idi1 isopentenyl-diphosphate delta isomerase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:16368707 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16368707 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11431693 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16368707 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16397868 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:16368707 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15459179 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:9590284 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:9590284 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9590284 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11431693 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16368707 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9590284 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11431693 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10400982 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9590284 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0003121 genetic imprinting IAGP N RGD:5509061 20141003 MGI PMID:16397868 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:15459179 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:16368707 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:9590284 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:16368707 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:9590284 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:16397868 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:21659337 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:16368707 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:21659337 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:21659337 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:9590284 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16368707 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15459179 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21659337 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9590284 735464 Snrpn small nuclear ribonucleoprotein N gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16368707 735466 Jag1 jagged 1 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:22156581 735466 Jag1 jagged 1 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:22156581 735466 Jag1 jagged 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:10196361 735466 Jag1 jagged 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20190905 MGI PMID:20720151 735466 Jag1 jagged 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19524514 735466 Jag1 jagged 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0000445 short snout IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0000486 abnormal pulmonary trunk morphology IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0000610 cholestasis IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0000610 cholestasis IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0000611 jaundice IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22156581 735466 Jag1 jagged 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0001306 small lens IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:10196361 735466 Jag1 jagged 1 gene MP:0001319 irregularly shaped pupil IAGP N RGD:5509061 20141003 MGI PMID:10196361 735466 Jag1 jagged 1 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:19389353 735466 Jag1 jagged 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:19389353 735466 Jag1 jagged 1 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:20081190 735466 Jag1 jagged 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:22156581 735466 Jag1 jagged 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:20081190 735466 Jag1 jagged 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:21068062 735466 Jag1 jagged 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19524514 735466 Jag1 jagged 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:22156581 735466 Jag1 jagged 1 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20190905 MGI PMID:20720151 735466 Jag1 jagged 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:10196361 735466 Jag1 jagged 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20190905 MGI PMID:20720151 735466 Jag1 jagged 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19524514 735466 Jag1 jagged 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:21068062 735466 Jag1 jagged 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10196361 735466 Jag1 jagged 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21068062 735466 Jag1 jagged 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20190905 MGI PMID:20720151 735466 Jag1 jagged 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10196361 735466 Jag1 jagged 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22156581 735466 Jag1 jagged 1 gene MP:0002083 premature death IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:10196361 735466 Jag1 jagged 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11181574 735466 Jag1 jagged 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17366661 735466 Jag1 jagged 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19217325 735466 Jag1 jagged 1 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:11181574 735466 Jag1 jagged 1 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16495313 735466 Jag1 jagged 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16495313 735466 Jag1 jagged 1 gene MP:0002729 abnormal inner ear canal morphology IAGP N RGD:5509061 20141003 MGI PMID:19389353 735466 Jag1 jagged 1 gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:11181574 735466 Jag1 jagged 1 gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19524514 735466 Jag1 jagged 1 gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:19389353 735466 Jag1 jagged 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18365007 735466 Jag1 jagged 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:21490058 735466 Jag1 jagged 1 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:18365007 735466 Jag1 jagged 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:11171333 735466 Jag1 jagged 1 gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:19389353 735466 Jag1 jagged 1 gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:21068062 735466 Jag1 jagged 1 gene MP:0003148 decreased cochlea coiling IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0003151 absent tunnel of Corti IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19524514 735466 Jag1 jagged 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11181574 735466 Jag1 jagged 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0003253 dilated bile duct IAGP N RGD:5509061 20141003 MGI PMID:17366661 735466 Jag1 jagged 1 gene MP:0003255 bile duct proliferation IAGP N RGD:5509061 20141003 MGI PMID:17366661 735466 Jag1 jagged 1 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11181574 735466 Jag1 jagged 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0003717 pallor IAGP N RGD:5509061 20190905 MGI PMID:20720151 735466 Jag1 jagged 1 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:22156581 735466 Jag1 jagged 1 gene MP:0003760 decreased palatal length IAGP N RGD:5509061 20141003 MGI PMID:22156581 735466 Jag1 jagged 1 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:10196361 735466 Jag1 jagged 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:21068062 735466 Jag1 jagged 1 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:21068062 735466 Jag1 jagged 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19524514 735466 Jag1 jagged 1 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:19389353 735466 Jag1 jagged 1 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16163386 735466 Jag1 jagged 1 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:16163386 735466 Jag1 jagged 1 gene MP:0004325 absent vestibular hair cells IAGP N RGD:5509061 20141003 MGI PMID:16495313 735466 Jag1 jagged 1 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:16495313 735466 Jag1 jagged 1 gene MP:0004336 small utricle IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:11181574 735466 Jag1 jagged 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16495313 735466 Jag1 jagged 1 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:11181574 735466 Jag1 jagged 1 gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0004403 absent cochlear outer hair cells IAGP N RGD:5509061 20141003 MGI PMID:16495313 735466 Jag1 jagged 1 gene MP:0004405 absent cochlear hair cells IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0004406 abnormal cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20141003 MGI PMID:17366661 735466 Jag1 jagged 1 gene MP:0004772 abnormal bile secretion IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:20081190 735466 Jag1 jagged 1 gene MP:0005083 abnormal biliary tract morphology IAGP N RGD:5509061 20141003 MGI PMID:21490058 735466 Jag1 jagged 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0005307 head tossing IEA N RGD:5509061 20111116 MGI 735466 Jag1 jagged 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0005356 positive geotaxis IAGP N RGD:5509061 20141003 MGI PMID:11181574 735466 Jag1 jagged 1 gene MP:0005419 decreased circulating serum albumin level IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21068062 735466 Jag1 jagged 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19524514 735466 Jag1 jagged 1 gene MP:0006048 pulmonary valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0006116 calcified aortic valve IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0006241 abnormal placement of pupils IAGP N RGD:5509061 20141003 MGI PMID:10196361 735466 Jag1 jagged 1 gene MP:0008137 absent podocytes IAGP N RGD:5509061 20141003 MGI PMID:23806616 735466 Jag1 jagged 1 gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20141003 MGI PMID:11181574 735466 Jag1 jagged 1 gene MP:0008488 abnormal semicircular canal ampulla morphology IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0008727 increased heart right atrium size IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:20081190 735466 Jag1 jagged 1 gene MP:0009654 abnormal primary palate development IAGP N RGD:5509061 20141003 MGI PMID:22156581 735466 Jag1 jagged 1 gene MP:0009820 abnormal liver vasculature morphology IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:20081190 735466 Jag1 jagged 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0010451 kidney microaneurysm IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0010457 pulmonary artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0010563 increased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0010714 iris coloboma IAGP N RGD:5509061 20141003 MGI PMID:10196361 735466 Jag1 jagged 1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16163386 735466 Jag1 jagged 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21068062 735466 Jag1 jagged 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11861489 735466 Jag1 jagged 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21068062 735466 Jag1 jagged 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10196361 735466 Jag1 jagged 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11181574 735466 Jag1 jagged 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16410827 735466 Jag1 jagged 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20081190 735466 Jag1 jagged 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21068062 735466 Jag1 jagged 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190905 MGI PMID:20720151 735466 Jag1 jagged 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:23806616 735466 Jag1 jagged 1 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:11171333 735466 Jag1 jagged 1 gene MP:0011648 thick heart valve cusps IAGP N RGD:5509061 20141003 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210211 MGI PMID:21062863 735466 Jag1 jagged 1 gene MP:0012024 abnormal nephron morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:23806616 735466 Jag1 jagged 1 gene MP:0012085 midface hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22156581 735466 Jag1 jagged 1 gene MP:0012236 abnormal cholangiocyte morphology IAGP N RGD:5509061 20190905 MGI PMID:29162437 735466 Jag1 jagged 1 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:11259677 735466 Jag1 jagged 1 gene MP:0021159 increased heart right ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:23095891 735466 Jag1 jagged 1 gene MP:0031114 increased circulating gamma-glutamyl transferase level IAGP N RGD:5509061 20210211 MGI PMID:21062863 735467 Sacm1l SAC1 suppressor of actin mutations 1-like (yeast) gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170105 MGI 735467 Sacm1l SAC1 suppressor of actin mutations 1-like (yeast) gene MP:0001147 small testis IEA N RGD:5509061 20170105 MGI 735467 Sacm1l SAC1 suppressor of actin mutations 1-like (yeast) gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 735467 Sacm1l SAC1 suppressor of actin mutations 1-like (yeast) gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20220630 MGI PMID:18480408 735467 Sacm1l SAC1 suppressor of actin mutations 1-like (yeast) gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20170105 MGI 735467 Sacm1l SAC1 suppressor of actin mutations 1-like (yeast) gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 735467 Sacm1l SAC1 suppressor of actin mutations 1-like (yeast) gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20170105 MGI 735467 Sacm1l SAC1 suppressor of actin mutations 1-like (yeast) gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20220630 MGI PMID:18480408 735467 Sacm1l SAC1 suppressor of actin mutations 1-like (yeast) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735467 Sacm1l SAC1 suppressor of actin mutations 1-like (yeast) gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20220630 MGI PMID:18480408 735467 Sacm1l SAC1 suppressor of actin mutations 1-like (yeast) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20221103 MGI 735467 Sacm1l SAC1 suppressor of actin mutations 1-like (yeast) gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 735467 Sacm1l SAC1 suppressor of actin mutations 1-like (yeast) gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000024 lowered ear position IAGP N RGD:5509061 20141003 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23685250 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17336904 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:23685250 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:23023706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24142516 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000425 loss of eyelid cilia IAGP N RGD:5509061 20141003 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:23685250 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:23685250 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:23328398 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20160225 MGI PMID:24855947 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:18653563 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20160225 MGI PMID:24855947 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20160225 MGI PMID:24855947 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17336904 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20170105 MGI 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001147 small testis IEA N RGD:5509061 20170105 MGI 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:21513708 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:23023706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19618463 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:21513708 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:23023706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19618463 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19618463 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001221 epidermal atrophy IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23685250 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23685250 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:23023706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:23023706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001652 colonic necrosis IAGP N RGD:5509061 20160225 MGI PMID:24855947 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:18653563 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23685250 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:23023706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20151112 MGI PMID:23358455 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:23328398 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17336904 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:23023706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20190912 MGI PMID:29844172 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23328398 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23685250 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:21513708 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19605684 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150903 MGI PMID:24894949 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20200507 MGI PMID:28346224 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:18990706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:17336904 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:17336904 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:23685250 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:18990706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0003190 fused synovial joints IAGP N RGD:5509061 20141003 MGI PMID:15371327 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17199045 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23685250 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20160609 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20190912 MGI PMID:29844172 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:19618463 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0003869 ectopic cartilage IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:23328398 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23023706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:24142516 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15030764 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:15030764 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20190912 MGI PMID:29844172 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0004551 decreased tracheal cartilage ring number IAGP N RGD:5509061 20141003 MGI PMID:18990706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0004606 absent vertebral spinous process IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18653563 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20160225 MGI PMID:24855947 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0004882 enlarged lung IAGP N RGD:5509061 20141003 MGI PMID:21513708 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20210429 MGI PMID:32491951 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0006236 absent Meibomian glands IAGP N RGD:5509061 20141003 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0006320 abnormal interscapular fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17199045 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23685250 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17336904 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0008274 failure of bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0008275 failure of endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17336904 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:15030764 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:17199045 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20160225 MGI PMID:24855947 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12756187 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0009571 abnormal right lung accessory lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:19618463 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0009572 abnormal right lung cranial lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:19618463 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0009573 abnormal right lung middle lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:19618463 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20191226 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0010678 abnormal skin adnexa morphology IAGP N RGD:5509061 20141003 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:23685250 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:21513708 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:24142516 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:18990706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0010880 small esophagus IAGP N RGD:5509061 20141003 MGI PMID:23328398 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:18990706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:19618463 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0010976 small lung lobe IAGP N RGD:5509061 20141003 MGI PMID:19618463 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0010988 abnormal bronchial cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:18990706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:18990706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19618463 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17336904 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23023706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12553906 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21513708 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18990706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23023706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011142 abnormal lung-associated mesenchyme development IAGP N RGD:5509061 20141003 MGI PMID:23023706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011156 abnormal hypodermis fat layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23685250 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011237 decreased blood oxygen capacity IAGP N RGD:5509061 20141003 MGI PMID:23023706 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011712 arrested osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:21924256 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0011772 genital tubercle hypoplasia IAGP N RGD:5509061 20151112 MGI PMID:23358455 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0013389 Meibomian gland hypoplasia IAGP N RGD:5509061 20141225 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0020148 abnormal susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20160225 MGI PMID:24855947 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0030009 increased bone marrow adipose tissue amount IAGP N RGD:5509061 20170706 MGI PMID:23685250 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0030191 narrow snout IAGP N RGD:5509061 20171019 MGI PMID:20691403 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0030393 delayed fontanelle closure IAGP N RGD:5509061 20171207 MGI PMID:15030764 735469 Twist2 twist basic helix-loop-helix transcription factor 2 gene MP:0031319 impaired intestine regeneration IAGP N RGD:5509061 20211125 MGI PMID:24855947 735471 Rcn2 reticulocalbin 2 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20191114 MGI PMID:30943068 735471 Rcn2 reticulocalbin 2 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20191114 MGI PMID:30943068 735471 Rcn2 reticulocalbin 2 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20191114 MGI PMID:30943068 735471 Rcn2 reticulocalbin 2 gene MP:0012046 decreased susceptibility to hypertension IAGP N RGD:5509061 20191114 MGI PMID:30943068 735474 Erp29 endoplasmic reticulum protein 29 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20191226 MGI PMID:24370996 735474 Erp29 endoplasmic reticulum protein 29 gene MP:0008407 decreased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20191226 MGI PMID:24370996 735474 Erp29 endoplasmic reticulum protein 29 gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20191226 MGI PMID:24370996 735477 Prdx2 peroxiredoxin 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0000256 echinocytosis IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0000314 schistocytosis IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0002812 spherocytosis IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:12586629 735477 Prdx2 peroxiredoxin 2 gene MP:0011171 increased number of Heinz bodies IAGP N RGD:5509061 20141003 MGI PMID:12586629 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18854157 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18854157 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19171781 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16357220 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:21826105 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:18854157 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18854157 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:14690604 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16357220 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16357220 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:14690604 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:16357220 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:18854157 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:14690604 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:18854157 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:14690604 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:16357220 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:18854157 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20141003 MGI PMID:21826105 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:14690604 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:16357220 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:18854157 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:19171781 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:21826105 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:21826105 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0008058 abnormal DNA repair IAGP N RGD:5509061 20141003 MGI PMID:18854157 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:14690604 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:18854157 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:21826105 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19171781 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20190124 MGI PMID:29973640 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18854157 735478 Mre11a MRE11A homolog A, double strand break repair nuclease gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16357220 735481 Atp9a ATPase, class II, type 9A gene MP:0001399 hyperactivity IAGP N RGD:5509061 20240321 MGI PMID:36604604 735481 Atp9a ATPase, class II, type 9A gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 735481 Atp9a ATPase, class II, type 9A gene MP:0001924 infertility IAGP N RGD:5509061 20240321 MGI PMID:36604604 735481 Atp9a ATPase, class II, type 9A gene MP:0002083 premature death IAGP N RGD:5509061 20240321 MGI PMID:36604604 735481 Atp9a ATPase, class II, type 9A gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20240321 MGI PMID:36604604 735481 Atp9a ATPase, class II, type 9A gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20240321 MGI PMID:36604604 735481 Atp9a ATPase, class II, type 9A gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20240321 MGI PMID:36604604 735481 Atp9a ATPase, class II, type 9A gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20240321 MGI PMID:36604604 735481 Atp9a ATPase, class II, type 9A gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20240321 MGI PMID:36604604 735481 Atp9a ATPase, class II, type 9A gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 735481 Atp9a ATPase, class II, type 9A gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20240321 MGI PMID:36604604 735481 Atp9a ATPase, class II, type 9A gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20240321 MGI PMID:36604604 735481 Atp9a ATPase, class II, type 9A gene MP:0021090 abnormal dendrite arborization pattern IAGP N RGD:5509061 20240321 MGI PMID:36604604 735483 Tph1 tryptophan hydroxylase 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:14597720 735483 Tph1 tryptophan hydroxylase 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:18923670 735483 Tph1 tryptophan hydroxylase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18923670 735483 Tph1 tryptophan hydroxylase 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:14597720 735483 Tph1 tryptophan hydroxylase 1 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:18923670 735483 Tph1 tryptophan hydroxylase 1 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:14597720 735483 Tph1 tryptophan hydroxylase 1 gene MP:0002899 fatigue IAGP N RGD:5509061 20141003 MGI PMID:14597720 735483 Tph1 tryptophan hydroxylase 1 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:14597720 735483 Tph1 tryptophan hydroxylase 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:18923670 735483 Tph1 tryptophan hydroxylase 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:14597720 735483 Tph1 tryptophan hydroxylase 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:18923670 735483 Tph1 tryptophan hydroxylase 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:19041748 735483 Tph1 tryptophan hydroxylase 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14597720 735483 Tph1 tryptophan hydroxylase 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20200402 MGI PMID:31806625 735483 Tph1 tryptophan hydroxylase 1 gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:18923670 735483 Tph1 tryptophan hydroxylase 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18923670 735483 Tph1 tryptophan hydroxylase 1 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:19041748 735483 Tph1 tryptophan hydroxylase 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20200402 MGI PMID:31806625 735483 Tph1 tryptophan hydroxylase 1 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20200402 MGI PMID:31806625 735483 Tph1 tryptophan hydroxylase 1 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20171221 MGI PMID:19041748 735483 Tph1 tryptophan hydroxylase 1 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:14597720 735483 Tph1 tryptophan hydroxylase 1 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:18923670 735483 Tph1 tryptophan hydroxylase 1 gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:14597720 735483 Tph1 tryptophan hydroxylase 1 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20200402 MGI PMID:31806625 735483 Tph1 tryptophan hydroxylase 1 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:14597720 735483 Tph1 tryptophan hydroxylase 1 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20171221 MGI PMID:19041748 735483 Tph1 tryptophan hydroxylase 1 gene MP:0030438 increased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:19041748 735484 Slit2 slit guidance ligand 2 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20170209 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:23328398 735484 Slit2 slit guidance ligand 2 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20170209 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:15130495 735484 Slit2 slit guidance ligand 2 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:15130495 735484 Slit2 slit guidance ligand 2 gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:15130495 735484 Slit2 slit guidance ligand 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210128 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:14605369 735484 Slit2 slit guidance ligand 2 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15084255 735484 Slit2 slit guidance ligand 2 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15091338 735484 Slit2 slit guidance ligand 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0003231 abnormal placenta vasculature IEA N RGD:5509061 20210128 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:16439476 735484 Slit2 slit guidance ligand 2 gene MP:0004017 duplex kidney IEA N RGD:5509061 20170209 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0004133 heterotaxia IEA N RGD:5509061 20170209 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:18054781 735484 Slit2 slit guidance ligand 2 gene MP:0005237 abnormal olfactory tract morphology IAGP N RGD:5509061 20141003 MGI PMID:17360927 735484 Slit2 slit guidance ligand 2 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:15130495 735484 Slit2 slit guidance ligand 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:18054781 735484 Slit2 slit guidance ligand 2 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20170209 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20160211 MGI PMID:24607227 735484 Slit2 slit guidance ligand 2 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16439476 735484 Slit2 slit guidance ligand 2 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18829537 735484 Slit2 slit guidance ligand 2 gene MP:0009678 abnormal spinal cord lateral column morphology IAGP N RGD:5509061 20141003 MGI PMID:15091338 735484 Slit2 slit guidance ligand 2 gene MP:0009695 abnormal spinal cord ventral commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:15091338 735484 Slit2 slit guidance ligand 2 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0009944 abnormal olfactory lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:17360927 735484 Slit2 slit guidance ligand 2 gene MP:0010173 increased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18829537 735484 Slit2 slit guidance ligand 2 gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20170209 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170209 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0010422 heart right ventricle hypoplasia IEA N RGD:5509061 20170209 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0010466 vascular ring IEA N RGD:5509061 20170209 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0010485 aortic arch hypoplasia IEA N RGD:5509061 20170209 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18054781 735484 Slit2 slit guidance ligand 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15130495 735484 Slit2 slit guidance ligand 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735484 Slit2 slit guidance ligand 2 gene MP:0011334 abnormal nephrogenic zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15130495 735487 Capns1 calpain, small subunit 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:10825211 735487 Capns1 calpain, small subunit 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:10825211 735487 Capns1 calpain, small subunit 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10825211 735487 Capns1 calpain, small subunit 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:21795695 735487 Capns1 calpain, small subunit 1 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:10825211 735487 Capns1 calpain, small subunit 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21795695 735487 Capns1 calpain, small subunit 1 gene MP:0003228 abnormal sinus venosus morphology IAGP N RGD:5509061 20141003 MGI PMID:10825211 735487 Capns1 calpain, small subunit 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10825211 735487 Capns1 calpain, small subunit 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21795695 735487 Capns1 calpain, small subunit 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:21795695 735487 Capns1 calpain, small subunit 1 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:21795695 735487 Capns1 calpain, small subunit 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21795695 735487 Capns1 calpain, small subunit 1 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:21795695 735487 Capns1 calpain, small subunit 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:21795695 735487 Capns1 calpain, small subunit 1 gene MP:0006207 embryonic lethality during organogenesis IEA N RGD:5509061 20160211 MGI 735487 Capns1 calpain, small subunit 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10825211 735487 Capns1 calpain, small subunit 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11087123 735487 Capns1 calpain, small subunit 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10825211 735487 Capns1 calpain, small subunit 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16783822 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:11115837 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:11115837 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:11115837 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:20430975 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:11099045 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:11115837 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:20430975 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20351103 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:11099045 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:11115837 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:20430975 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11099045 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11115837 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:20430975 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:11115837 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:11115837 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0005060 accumulation of giant lysosomes in kidney/renal tubule cells IAGP N RGD:5509061 20141003 MGI PMID:19661288 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:12548389 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:11115837 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:20430975 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20430975 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:11099045 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:20430975 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0011376 abnormal kidney corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:11115837 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0011417 abnormal renal transport IAGP N RGD:5509061 20141003 MGI PMID:11099045 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0011417 abnormal renal transport IAGP N RGD:5509061 20141003 MGI PMID:12548389 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0011445 abnormal renal protein reabsorption IAGP N RGD:5509061 20141003 MGI PMID:11115837 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0011445 abnormal renal protein reabsorption IAGP N RGD:5509061 20141003 MGI PMID:12815097 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0011445 abnormal renal protein reabsorption IAGP N RGD:5509061 20141003 MGI PMID:20351103 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:20430975 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0011556 increased urine beta2-microglobulin level IAGP N RGD:5509061 20141003 MGI PMID:11099045 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0011559 increased urine insulin level IAGP N RGD:5509061 20141003 MGI PMID:20430975 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0020400 cystinuria IAGP N RGD:5509061 20161208 MGI PMID:11115837 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0020406 hyperthreoninuria IAGP N RGD:5509061 20161208 MGI PMID:11115837 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0030617 hyperglutaminuria IAGP N RGD:5509061 20180906 MGI PMID:11115837 735491 Clcn5 chloride channel, voltage-sensitive 5 gene MP:0030682 hydroxyprolinuria IAGP N RGD:5509061 20180920 MGI PMID:11115837 735497 Kif2a kinesin family member 2A gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0000848 abnormal pons morphology IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0000906 abnormal trigeminal V mesencephalic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 735497 Kif2a kinesin family member 2A gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0003684 abnormal inferior olivary complex morphology IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0006100 abnormal tegmentum morphology IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 735497 Kif2a kinesin family member 2A gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:12887924 735497 Kif2a kinesin family member 2A gene MP:0020560 abnormal pontine nuclei morphology IAGP N RGD:5509061 20180315 MGI PMID:12887924 735500 Foxe1 forkhead box E1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:9697704 735500 Foxe1 forkhead box E1 gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:15367491 735500 Foxe1 forkhead box E1 gene MP:0000396 increased curvature of hairs IAGP N RGD:5509061 20141003 MGI PMID:15367491 735500 Foxe1 forkhead box E1 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:15367491 735500 Foxe1 forkhead box E1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:15367491 735500 Foxe1 forkhead box E1 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:15367491 735500 Foxe1 forkhead box E1 gene MP:0003351 decreased circulating levels of thyroid hormone IAGP N RGD:5509061 20141003 MGI PMID:9697704 735500 Foxe1 forkhead box E1 gene MP:0003421 abnormal thyroid gland development IAGP N RGD:5509061 20141003 MGI PMID:15581879 735500 Foxe1 forkhead box E1 gene MP:0003421 abnormal thyroid gland development IAGP N RGD:5509061 20141003 MGI PMID:9697704 735500 Foxe1 forkhead box E1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:15367491 735500 Foxe1 forkhead box E1 gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:9697704 735500 Foxe1 forkhead box E1 gene MP:0005314 absent thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:9697704 735500 Foxe1 forkhead box E1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:9697704 735500 Foxe1 forkhead box E1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9697704 735502 Ntn1 netrin 1 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:12636918 735502 Ntn1 netrin 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:8978605 735502 Ntn1 netrin 1 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:10654596 735502 Ntn1 netrin 1 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:8978605 735502 Ntn1 netrin 1 gene MP:0002859 abnormal inner ear canal fusion IAGP N RGD:5509061 20141003 MGI PMID:10654596 735502 Ntn1 netrin 1 gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20141003 MGI PMID:8978605 735502 Ntn1 netrin 1 gene MP:0002878 abnormal corticospinal tract morphology IAGP N RGD:5509061 20141003 MGI PMID:12451134 735502 Ntn1 netrin 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:10477289 735502 Ntn1 netrin 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20160414 MGI PMID:26257176 735502 Ntn1 netrin 1 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:10654596 735502 Ntn1 netrin 1 gene MP:0003163 absent posterior semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:10654596 735502 Ntn1 netrin 1 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:8978605 735502 Ntn1 netrin 1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:16439476 735502 Ntn1 netrin 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:10477289 735502 Ntn1 netrin 1 gene MP:0003994 abnormal dorsal spinal root morphology IAGP N RGD:5509061 20160414 MGI PMID:26257176 735502 Ntn1 netrin 1 gene MP:0005262 coloboma IAGP N RGD:5509061 20221103 MGI PMID:31162046 735502 Ntn1 netrin 1 gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:8978605 735502 Ntn1 netrin 1 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:8978605 735502 Ntn1 netrin 1 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16439476 735502 Ntn1 netrin 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:10654596 735502 Ntn1 netrin 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:8978605 735502 Ntn1 netrin 1 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:12451134 735502 Ntn1 netrin 1 gene MP:0009681 abnormal pyramidal decussation morphology IAGP N RGD:5509061 20141003 MGI PMID:12451134 735502 Ntn1 netrin 1 gene MP:0009688 abnormal spinal cord central canal morphology IAGP N RGD:5509061 20160414 MGI PMID:26257176 735502 Ntn1 netrin 1 gene MP:0009695 abnormal spinal cord ventral commissure morphology IAGP N RGD:5509061 20160414 MGI PMID:26257176 735502 Ntn1 netrin 1 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20221103 MGI PMID:31162046 735502 Ntn1 netrin 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221103 MGI PMID:31162046 735502 Ntn1 netrin 1 gene MP:0010151 abnormal spinal cord ependymal layer morphology IAGP N RGD:5509061 20160414 MGI PMID:26257176 735502 Ntn1 netrin 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8978605 735502 Ntn1 netrin 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10654596 735502 Ntn1 netrin 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12636918 735502 Ntn1 netrin 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20160414 MGI PMID:26257176 735502 Ntn1 netrin 1 gene MP:0020560 abnormal pontine nuclei morphology IAGP N RGD:5509061 20180315 MGI PMID:8978605 735503 Psme1 proteasome (prosome, macropain) activator subunit 1 (PA28 alpha) gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20181227 MGI 735503 Psme1 proteasome (prosome, macropain) activator subunit 1 (PA28 alpha) gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:16569681 735507 Sct secretin gene MP:0001422 abnormal drinking behavior IAGP N RGD:5509061 20141003 MGI PMID:20739612 735507 Sct secretin gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18534766 735507 Sct secretin gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:18534766 735507 Sct secretin gene MP:0002922 decreased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:18534766 735507 Sct secretin gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:20739612 735507 Sct secretin gene MP:0005609 abnormal circulating antidiuretic hormone level IAGP N RGD:5509061 20141003 MGI PMID:20739612 735510 Map1b microtubule-associated protein 1B gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:11085878 735510 Map1b microtubule-associated protein 1B gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:11581286 735510 Map1b microtubule-associated protein 1B gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11085878 735510 Map1b microtubule-associated protein 1B gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11581286 735510 Map1b microtubule-associated protein 1B gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:11581286 735510 Map1b microtubule-associated protein 1B gene MP:0000794 abnormal parietal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:11085878 735510 Map1b microtubule-associated protein 1B gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:11085878 735510 Map1b microtubule-associated protein 1B gene MP:0000813 abnormal hippocampus layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11581286 735510 Map1b microtubule-associated protein 1B gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:11085878 735510 Map1b microtubule-associated protein 1B gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:11085878 735510 Map1b microtubule-associated protein 1B gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:11085878 735510 Map1b microtubule-associated protein 1B gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0001061 abnormal oculomotor nerve morphology IAGP N RGD:5509061 20181122 MGI PMID:24656932 735510 Map1b microtubule-associated protein 1B gene MP:0001070 abnormal abducens nerve morphology IAGP N RGD:5509061 20181122 MGI PMID:24656932 735510 Map1b microtubule-associated protein 1B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200123 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20181122 MGI PMID:24656932 735510 Map1b microtubule-associated protein 1B gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11085878 735510 Map1b microtubule-associated protein 1B gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20181122 MGI PMID:24656932 735510 Map1b microtubule-associated protein 1B gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:11581286 735510 Map1b microtubule-associated protein 1B gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11581286 735510 Map1b microtubule-associated protein 1B gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:15306655 735510 Map1b microtubule-associated protein 1B gene MP:0003684 abnormal inferior olivary complex morphology IAGP N RGD:5509061 20141003 MGI PMID:11581286 735510 Map1b microtubule-associated protein 1B gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:11581286 735510 Map1b microtubule-associated protein 1B gene MP:0004167 abnormal cingulate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:11085878 735510 Map1b microtubule-associated protein 1B gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20200123 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:11581286 735510 Map1b microtubule-associated protein 1B gene MP:0008443 absent subplate IAGP N RGD:5509061 20141003 MGI PMID:11085878 735510 Map1b microtubule-associated protein 1B gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:11085878 735510 Map1b microtubule-associated protein 1B gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:11085878 735510 Map1b microtubule-associated protein 1B gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:8577753 735510 Map1b microtubule-associated protein 1B gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11121433 735510 Map1b microtubule-associated protein 1B gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11085878 735510 Map1b microtubule-associated protein 1B gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11581286 735510 Map1b microtubule-associated protein 1B gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8577753 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22001390 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17062731 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0000238 absent pre-B cells IAGP N RGD:5509061 20141003 MGI PMID:14668867 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:17062731 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:22001390 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:14668867 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0000727 absent CD8-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:18566418 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20201022 MGI 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10640272 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14668867 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18566418 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14668867 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20211202 MGI PMID:22001390 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20201022 MGI 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14668867 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20929728 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18566418 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14668867 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0002188 small heart IEA N RGD:5509061 20210826 MGI 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19234191 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:17062731 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0002607 decreased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22001390 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:22001390 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22001390 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:10640272 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0003790 absent CD4-positive, alpha-beta T cells IAGP N RGD:5509061 20141003 MGI PMID:18566418 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19234191 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:17062731 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:14668867 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:14668867 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:18566418 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:14668867 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:18566418 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:19234191 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18566418 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:14668867 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18566418 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0005433 absent early pro-B cells IAGP N RGD:5509061 20141003 MGI PMID:14668867 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0005434 absent late pro-B cells IAGP N RGD:5509061 20141003 MGI PMID:14668867 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:22001390 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14668867 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18566418 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18566418 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19234191 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18566418 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19234191 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19234191 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0008094 absent memory B cells IAGP N RGD:5509061 20141003 MGI PMID:20929728 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:20929728 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0008179 absent germinal center B cells IAGP N RGD:5509061 20141003 MGI PMID:20929728 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0008185 decreased naive B cell number IAGP N RGD:5509061 20141003 MGI PMID:20929728 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20929728 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:17062731 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0008729 decreased memory B cell number IAGP N RGD:5509061 20141003 MGI PMID:20929728 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0008782 increased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14668867 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20141003 MGI PMID:10640272 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10640272 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10640272 735513 Mcl1 myeloid cell leukemia sequence 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 735515 Pdcl phosducin-like gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:23637185 735515 Pdcl phosducin-like gene MP:0001999 photosensitivity IAGP N RGD:5509061 20141003 MGI PMID:23637185 735515 Pdcl phosducin-like gene MP:0003011 delayed dark adaptation IAGP N RGD:5509061 20141003 MGI PMID:23637185 735515 Pdcl phosducin-like gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:23637185 735515 Pdcl phosducin-like gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20141003 MGI PMID:23637185 735515 Pdcl phosducin-like gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:23637185 735515 Pdcl phosducin-like gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:23637185 735515 Pdcl phosducin-like gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20141003 MGI PMID:23637185 735515 Pdcl phosducin-like gene MP:0014336 short retina rod cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:23637185 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15564292 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0001354 increased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:16247016 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:16247016 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20111116 MGI 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:16247016 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17710229 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:20092576 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:11375261 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:17967902 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0002351 abnormal cervical lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:17967902 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11160156 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0002664 decreased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:12642666 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:11160156 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11160156 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:16885154 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16247016 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:15564292 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:17710229 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20141003 MGI PMID:12837930 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:16885154 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15564292 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17710229 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17710229 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:12642666 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0005407 hyperalgesia IAGP N RGD:5509061 20141003 MGI PMID:11375261 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0005582 increased renin activity IAGP N RGD:5509061 20141003 MGI PMID:11160156 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:17967902 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:16247016 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17710229 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:17710229 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17967902 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17967902 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11160156 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0008559 abnormal interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17967902 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11966527 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15564292 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11966527 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10537280 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0010698 abnormal impulsive behavior control IAGP N RGD:5509061 20141003 MGI PMID:16247016 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:17710229 735522 Ptger1 prostaglandin E receptor 1 (subtype EP1) gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:17710229 735524 Hspb8 heat shock protein 8 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 735524 Hspb8 heat shock protein 8 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:21747053 735524 Hspb8 heat shock protein 8 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20210826 MGI 735524 Hspb8 heat shock protein 8 gene MP:0000751 myopathy IAGP N RGD:5509061 20200402 MGI PMID:28780615 735524 Hspb8 heat shock protein 8 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20200402 MGI PMID:28780615 735524 Hspb8 heat shock protein 8 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 735524 Hspb8 heat shock protein 8 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200402 MGI PMID:28780615 735524 Hspb8 heat shock protein 8 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21747053 735524 Hspb8 heat shock protein 8 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20220811 MGI 735524 Hspb8 heat shock protein 8 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21747053 735524 Hspb8 heat shock protein 8 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20200402 MGI PMID:28780615 735524 Hspb8 heat shock protein 8 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20200402 MGI PMID:28780615 735524 Hspb8 heat shock protein 8 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20200402 MGI PMID:28780615 735524 Hspb8 heat shock protein 8 gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:21747053 735524 Hspb8 heat shock protein 8 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20200402 MGI PMID:28780615 735524 Hspb8 heat shock protein 8 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20200402 MGI PMID:28780615 735524 Hspb8 heat shock protein 8 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:21747053 735524 Hspb8 heat shock protein 8 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20200402 MGI PMID:28780615 735524 Hspb8 heat shock protein 8 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20200402 MGI PMID:28780615 735524 Hspb8 heat shock protein 8 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21747053 735524 Hspb8 heat shock protein 8 gene MP:0005630 increased lung weight IAGP N RGD:5509061 20141003 MGI PMID:21747053 735524 Hspb8 heat shock protein 8 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21747053 735524 Hspb8 heat shock protein 8 gene MP:0009412 skeletal muscle fiber degeneration IAGP N RGD:5509061 20200402 MGI PMID:28780615 735524 Hspb8 heat shock protein 8 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21747053 735524 Hspb8 heat shock protein 8 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200402 MGI PMID:28780615 735524 Hspb8 heat shock protein 8 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:21747053 735524 Hspb8 heat shock protein 8 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:21747053 735524 Hspb8 heat shock protein 8 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:21747053 735524 Hspb8 heat shock protein 8 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20210128 MGI 735524 Hspb8 heat shock protein 8 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20200402 MGI PMID:28780615 735526 Mc4r melanocortin 4 receptor gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:23374353 735526 Mc4r melanocortin 4 receptor gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:16269339 735526 Mc4r melanocortin 4 receptor gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:23374353 735526 Mc4r melanocortin 4 receptor gene MP:0001257 increased body length IAGP N RGD:5509061 20150129 MGI PMID:25157144 735526 Mc4r melanocortin 4 receptor gene MP:0001257 increased body length IAGP N RGD:5509061 20160218 MGI PMID:21969101 735526 Mc4r melanocortin 4 receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:10973258 735526 Mc4r melanocortin 4 receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12697680 735526 Mc4r melanocortin 4 receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15596147 735526 Mc4r melanocortin 4 receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16269339 735526 Mc4r melanocortin 4 receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16720677 735526 Mc4r melanocortin 4 receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17143585 735526 Mc4r melanocortin 4 receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:9019399 735526 Mc4r melanocortin 4 receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20150129 MGI PMID:25157144 735526 Mc4r melanocortin 4 receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20160218 MGI PMID:21969101 735526 Mc4r melanocortin 4 receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:16269339 735526 Mc4r melanocortin 4 receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:16720677 735526 Mc4r melanocortin 4 receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:17143585 735526 Mc4r melanocortin 4 receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:21906580 735526 Mc4r melanocortin 4 receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:23374353 735526 Mc4r melanocortin 4 receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:23869016 735526 Mc4r melanocortin 4 receptor gene MP:0001261 obese IAGP N RGD:5509061 20150129 MGI PMID:25157144 735526 Mc4r melanocortin 4 receptor gene MP:0001261 obese IAGP N RGD:5509061 20160218 MGI PMID:21969101 735526 Mc4r melanocortin 4 receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17143585 735526 Mc4r melanocortin 4 receptor gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:9019399 735526 Mc4r melanocortin 4 receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:12697680 735526 Mc4r melanocortin 4 receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:15596147 735526 Mc4r melanocortin 4 receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:16269339 735526 Mc4r melanocortin 4 receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:19036977 735526 Mc4r melanocortin 4 receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:9019399 735526 Mc4r melanocortin 4 receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20150129 MGI PMID:25157144 735526 Mc4r melanocortin 4 receptor gene MP:0001433 polyphagia IAGP N RGD:5509061 20160218 MGI PMID:21969101 735526 Mc4r melanocortin 4 receptor gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21906580 735526 Mc4r melanocortin 4 receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12955145 735526 Mc4r melanocortin 4 receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:9019399 735526 Mc4r melanocortin 4 receptor gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:21906580 735526 Mc4r melanocortin 4 receptor gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200507 MGI PMID:31990961 735526 Mc4r melanocortin 4 receptor gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15596147 735526 Mc4r melanocortin 4 receptor gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9019399 735526 Mc4r melanocortin 4 receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16269339 735526 Mc4r melanocortin 4 receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:23374353 735526 Mc4r melanocortin 4 receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9019399 735526 Mc4r melanocortin 4 receptor gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20200507 MGI PMID:31990961 735526 Mc4r melanocortin 4 receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16269339 735526 Mc4r melanocortin 4 receptor gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23374353 735526 Mc4r melanocortin 4 receptor gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200507 MGI PMID:31990961 735526 Mc4r melanocortin 4 receptor gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:21906580 735526 Mc4r melanocortin 4 receptor gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200507 MGI PMID:31990961 735526 Mc4r melanocortin 4 receptor gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:21906580 735526 Mc4r melanocortin 4 receptor gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200507 MGI PMID:31990961 735526 Mc4r melanocortin 4 receptor gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:15596147 735526 Mc4r melanocortin 4 receptor gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21906580 735526 Mc4r melanocortin 4 receptor gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21906580 735526 Mc4r melanocortin 4 receptor gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200507 MGI PMID:31990961 735526 Mc4r melanocortin 4 receptor gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:16269339 735526 Mc4r melanocortin 4 receptor gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23374353 735526 Mc4r melanocortin 4 receptor gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20160218 MGI PMID:21969101 735526 Mc4r melanocortin 4 receptor gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20160218 MGI PMID:21969101 735526 Mc4r melanocortin 4 receptor gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20160218 MGI PMID:21969101 735526 Mc4r melanocortin 4 receptor gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:15724149 735526 Mc4r melanocortin 4 receptor gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200507 MGI PMID:31990961 735526 Mc4r melanocortin 4 receptor gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:16269339 735526 Mc4r melanocortin 4 receptor gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:16269339 735526 Mc4r melanocortin 4 receptor gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20160218 MGI PMID:21969101 735526 Mc4r melanocortin 4 receptor gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200507 MGI PMID:31990961 735526 Mc4r melanocortin 4 receptor gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:10971147 735526 Mc4r melanocortin 4 receptor gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:15034587 735526 Mc4r melanocortin 4 receptor gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:16269339 735526 Mc4r melanocortin 4 receptor gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:12955145 735526 Mc4r melanocortin 4 receptor gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:16720677 735526 Mc4r melanocortin 4 receptor gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:21906580 735526 Mc4r melanocortin 4 receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17143585 735526 Mc4r melanocortin 4 receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18719666 735526 Mc4r melanocortin 4 receptor gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:15724149 735526 Mc4r melanocortin 4 receptor gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:11369941 735526 Mc4r melanocortin 4 receptor gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:21906580 735526 Mc4r melanocortin 4 receptor gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200507 MGI PMID:31990961 735526 Mc4r melanocortin 4 receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21906580 735526 Mc4r melanocortin 4 receptor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:9019399 735526 Mc4r melanocortin 4 receptor gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:19036977 735526 Mc4r melanocortin 4 receptor gene MP:0006087 increased body mass index IEA N RGD:5509061 20170824 MGI 735526 Mc4r melanocortin 4 receptor gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21906580 735526 Mc4r melanocortin 4 receptor gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20160218 MGI PMID:21969101 735526 Mc4r melanocortin 4 receptor gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21906580 735526 Mc4r melanocortin 4 receptor gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20200507 MGI PMID:31990961 735526 Mc4r melanocortin 4 receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21906580 735526 Mc4r melanocortin 4 receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20150129 MGI PMID:25157144 735526 Mc4r melanocortin 4 receptor gene MP:0011939 increased food intake IAGP N RGD:5509061 20200507 MGI PMID:31990961 735526 Mc4r melanocortin 4 receptor gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:15596147 735526 Mc4r melanocortin 4 receptor gene MP:0030678 increased hydroxyproline level IAGP N RGD:5509061 20200507 MGI PMID:31990961 735526 Mc4r melanocortin 4 receptor gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:21906580 735526 Mc4r melanocortin 4 receptor gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:21906580 735526 Mc4r melanocortin 4 receptor gene MP:0031602 white adipose tissue inflammation IAGP N RGD:5509061 20240321 MGI PMID:21906580 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0008897 decreased IgG2c level IAGP N RGD:5509061 20210506 MGI PMID:32547538 735530 Hspa13 heat shock protein 70 family, member 13 gene MP:0013940 abnormal plasmablast number IAGP N RGD:5509061 20210506 MGI PMID:32547538 735533 C1qbp complement component 1, q subcomponent binding protein gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22904065 735533 C1qbp complement component 1, q subcomponent binding protein gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22904065 735533 C1qbp complement component 1, q subcomponent binding protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:22904065 735533 C1qbp complement component 1, q subcomponent binding protein gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22904065 735533 C1qbp complement component 1, q subcomponent binding protein gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:22904065 735533 C1qbp complement component 1, q subcomponent binding protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22904065 735535 Gjb3 gap junction protein, beta 3 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 735535 Gjb3 gap junction protein, beta 3 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 735535 Gjb3 gap junction protein, beta 3 gene MP:0000603 pale liver IEA N RGD:5509061 20210520 MGI 735535 Gjb3 gap junction protein, beta 3 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:17446259 735535 Gjb3 gap junction protein, beta 3 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17446259 735535 Gjb3 gap junction protein, beta 3 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20200402 MGI 735535 Gjb3 gap junction protein, beta 3 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:11237463 735535 Gjb3 gap junction protein, beta 3 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:11237463 735535 Gjb3 gap junction protein, beta 3 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 735535 Gjb3 gap junction protein, beta 3 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:17446259 735535 Gjb3 gap junction protein, beta 3 gene MP:0003717 pallor IEA N RGD:5509061 20220519 MGI 735535 Gjb3 gap junction protein, beta 3 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 735535 Gjb3 gap junction protein, beta 3 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:11237463 735535 Gjb3 gap junction protein, beta 3 gene MP:0004560 abnormal chorionic plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11237463 735535 Gjb3 gap junction protein, beta 3 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 735535 Gjb3 gap junction protein, beta 3 gene MP:0009931 abnormal skin appearance IEA N RGD:5509061 20200402 MGI 735535 Gjb3 gap junction protein, beta 3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17446259 735535 Gjb3 gap junction protein, beta 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735535 Gjb3 gap junction protein, beta 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11237463 735535 Gjb3 gap junction protein, beta 3 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20200402 MGI 735535 Gjb3 gap junction protein, beta 3 gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20141003 MGI PMID:11237463 735535 Gjb3 gap junction protein, beta 3 gene MP:0011525 abnormal placenta intervillous maternal lacunae morphology IAGP N RGD:5509061 20141003 MGI PMID:11237463 735535 Gjb3 gap junction protein, beta 3 gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:11237463 735537 Krt8 keratin 8 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 735537 Krt8 keratin 8 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:7686525 735537 Krt8 keratin 8 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11171325 735537 Krt8 keratin 8 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:7528156 735537 Krt8 keratin 8 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:15007064 735537 Krt8 keratin 8 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:7528156 735537 Krt8 keratin 8 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11514590 735537 Krt8 keratin 8 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11732007 735537 Krt8 keratin 8 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14576356 735537 Krt8 keratin 8 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9403718 735537 Krt8 keratin 8 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7528156 735537 Krt8 keratin 8 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15007064 735537 Krt8 keratin 8 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 735537 Krt8 keratin 8 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:7686525 735537 Krt8 keratin 8 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:14576356 735537 Krt8 keratin 8 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:7528156 735537 Krt8 keratin 8 gene MP:0001670 abnormal intestinal mineral absorption IAGP N RGD:5509061 20141003 MGI PMID:15007064 735537 Krt8 keratin 8 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 735537 Krt8 keratin 8 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:12771125 735537 Krt8 keratin 8 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 735537 Krt8 keratin 8 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 735537 Krt8 keratin 8 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:7686525 735537 Krt8 keratin 8 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:7528156 735537 Krt8 keratin 8 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:14576356 735537 Krt8 keratin 8 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:15840656 735537 Krt8 keratin 8 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:14576356 735537 Krt8 keratin 8 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14576356 735537 Krt8 keratin 8 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11062258 735537 Krt8 keratin 8 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 735537 Krt8 keratin 8 gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:11062258 735537 Krt8 keratin 8 gene MP:0004264 abnormal extraembryonic tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:12771125 735537 Krt8 keratin 8 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 735537 Krt8 keratin 8 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12771125 735537 Krt8 keratin 8 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 735537 Krt8 keratin 8 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12771125 735537 Krt8 keratin 8 gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:15007064 735537 Krt8 keratin 8 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20210128 MGI 735537 Krt8 keratin 8 gene MP:0006372 impaired placental function IAGP N RGD:5509061 20141003 MGI PMID:11062258 735537 Krt8 keratin 8 gene MP:0006372 impaired placental function IAGP N RGD:5509061 20141003 MGI PMID:12771125 735537 Krt8 keratin 8 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 735537 Krt8 keratin 8 gene MP:0008959 abnormal spongiotrophoblast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11062258 735537 Krt8 keratin 8 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20211021 MGI 735537 Krt8 keratin 8 gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:11062258 735537 Krt8 keratin 8 gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:7686525 735537 Krt8 keratin 8 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11062258 735537 Krt8 keratin 8 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735537 Krt8 keratin 8 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12771125 735537 Krt8 keratin 8 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12771125 735537 Krt8 keratin 8 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7528156 735537 Krt8 keratin 8 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7686525 735537 Krt8 keratin 8 gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20191219 MGI PMID:11062258 735540 Axin2 axin 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15790973 735540 Axin2 axin 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:21555575 735540 Axin2 axin 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24315444 735540 Axin2 axin 2 gene MP:0000435 shortened head IAGP N RGD:5509061 20141003 MGI PMID:15790973 735540 Axin2 axin 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15790973 735540 Axin2 axin 2 gene MP:0000562 polydactyly IEA N RGD:5509061 20210520 MGI 735540 Axin2 axin 2 gene MP:0000585 kinked tail IEA N RGD:5509061 20150910 MGI 735540 Axin2 axin 2 gene MP:0000653 abnormal sex gland morphology IAGP N RGD:5509061 20141003 MGI PMID:18250098 735540 Axin2 axin 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21555575 735540 Axin2 axin 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21555575 735540 Axin2 axin 2 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 735540 Axin2 axin 2 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 735540 Axin2 axin 2 gene MP:0001306 small lens IAGP N RGD:5509061 20191219 MGI PMID:27701636 735540 Axin2 axin 2 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 735540 Axin2 axin 2 gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20210520 MGI 735540 Axin2 axin 2 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 735540 Axin2 axin 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:21555575 735540 Axin2 axin 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180222 MGI PMID:28875532 735540 Axin2 axin 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:15790973 735540 Axin2 axin 2 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20181227 MGI 735540 Axin2 axin 2 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:21555575 735540 Axin2 axin 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:15790973 735540 Axin2 axin 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21555575 735540 Axin2 axin 2 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:21555575 735540 Axin2 axin 2 gene MP:0003051 curly tail IAGP N RGD:5509061 20180222 MGI PMID:28875532 735540 Axin2 axin 2 gene MP:0003385 abnormal body wall morphology IEA N RGD:5509061 20181227 MGI 735540 Axin2 axin 2 gene MP:0003418 premature intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15790973 735540 Axin2 axin 2 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20181227 MGI 735540 Axin2 axin 2 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:21555575 735540 Axin2 axin 2 gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20191219 MGI PMID:27701636 735540 Axin2 axin 2 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:15790973 735540 Axin2 axin 2 gene MP:0005262 coloboma IAGP N RGD:5509061 20191219 MGI PMID:27701636 735540 Axin2 axin 2 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21555575 735540 Axin2 axin 2 gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20141003 MGI PMID:21555575 735540 Axin2 axin 2 gene MP:0008525 decreased cranium height IAGP N RGD:5509061 20141003 MGI PMID:15790973 735540 Axin2 axin 2 gene MP:0009263 abnormal eyelid fusion IEA N RGD:5509061 20210520 MGI 735540 Axin2 axin 2 gene MP:0009908 protruding tongue IEA N RGD:5509061 20210520 MGI 735540 Axin2 axin 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735540 Axin2 axin 2 gene MP:0011101 prenatal lethality, incomplete penetrance IEA N RGD:5509061 20150910 MGI 735540 Axin2 axin 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21555575 735540 Axin2 axin 2 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 735540 Axin2 axin 2 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20181227 MGI 735540 Axin2 axin 2 gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:15790973 735540 Axin2 axin 2 gene MP:0030367 premature metopic suture closure IAGP N RGD:5509061 20171207 MGI PMID:15790973 735540 Axin2 axin 2 gene MP:0030370 absent jugum limitans IAGP N RGD:5509061 20171207 MGI PMID:15790973 735540 Axin2 axin 2 gene MP:0030438 increased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:15790973 735545 Neurod1 neurogenic differentiation 1 gene MP:0000436 abnormal head movements IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:9308961 735545 Neurod1 neurogenic differentiation 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:10804213 735545 Neurod1 neurogenic differentiation 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:10398678 735545 Neurod1 neurogenic differentiation 1 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:10804213 735545 Neurod1 neurogenic differentiation 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:23293286 735545 Neurod1 neurogenic differentiation 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:10398678 735545 Neurod1 neurogenic differentiation 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:10398678 735545 Neurod1 neurogenic differentiation 1 gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:10398678 735545 Neurod1 neurogenic differentiation 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10398678 735545 Neurod1 neurogenic differentiation 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:10398678 735545 Neurod1 neurogenic differentiation 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10398678 735545 Neurod1 neurogenic differentiation 1 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:11152640 735545 Neurod1 neurogenic differentiation 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:23293286 735545 Neurod1 neurogenic differentiation 1 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23293286 735545 Neurod1 neurogenic differentiation 1 gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20141003 MGI PMID:18339630 735545 Neurod1 neurogenic differentiation 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10398678 735545 Neurod1 neurogenic differentiation 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9308961 735545 Neurod1 neurogenic differentiation 1 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11861467 735545 Neurod1 neurogenic differentiation 1 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:23293286 735545 Neurod1 neurogenic differentiation 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10398678 735545 Neurod1 neurogenic differentiation 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:23293286 735545 Neurod1 neurogenic differentiation 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:9308961 735545 Neurod1 neurogenic differentiation 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:10398678 735545 Neurod1 neurogenic differentiation 1 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:10398678 735545 Neurod1 neurogenic differentiation 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:10398678 735545 Neurod1 neurogenic differentiation 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:9308961 735545 Neurod1 neurogenic differentiation 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10398678 735545 Neurod1 neurogenic differentiation 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10804213 735545 Neurod1 neurogenic differentiation 1 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11152640 735545 Neurod1 neurogenic differentiation 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:10804213 735545 Neurod1 neurogenic differentiation 1 gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11152640 735545 Neurod1 neurogenic differentiation 1 gene MP:0002893 ketoaciduria IAGP N RGD:5509061 20141003 MGI PMID:9308961 735545 Neurod1 neurogenic differentiation 1 gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:11861467 735545 Neurod1 neurogenic differentiation 1 gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:23293286 735545 Neurod1 neurogenic differentiation 1 gene MP:0003146 absent cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:11152640 735545 Neurod1 neurogenic differentiation 1 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11152640 735545 Neurod1 neurogenic differentiation 1 gene MP:0003310 reduced cochlear modiolus IAGP N RGD:5509061 20141003 MGI PMID:11152640 735545 Neurod1 neurogenic differentiation 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:9308961 735545 Neurod1 neurogenic differentiation 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:10804213 735545 Neurod1 neurogenic differentiation 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:10804213 735545 Neurod1 neurogenic differentiation 1 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11152640 735545 Neurod1 neurogenic differentiation 1 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23293286 735545 Neurod1 neurogenic differentiation 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23293286 735545 Neurod1 neurogenic differentiation 1 gene MP:0004410 absent endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:11152640 735545 Neurod1 neurogenic differentiation 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:10804213 735545 Neurod1 neurogenic differentiation 1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:23293286 735545 Neurod1 neurogenic differentiation 1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9308961 735545 Neurod1 neurogenic differentiation 1 gene MP:0005240 abnormal amacrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9834183 735545 Neurod1 neurogenic differentiation 1 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11861467 735545 Neurod1 neurogenic differentiation 1 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23293286 735545 Neurod1 neurogenic differentiation 1 gene MP:0005307 head tossing IEA N RGD:5509061 20180215 MGI 735545 Neurod1 neurogenic differentiation 1 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11861467 735545 Neurod1 neurogenic differentiation 1 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9834183 735545 Neurod1 neurogenic differentiation 1 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:18339630 735545 Neurod1 neurogenic differentiation 1 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9834183 735545 Neurod1 neurogenic differentiation 1 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9834183 735545 Neurod1 neurogenic differentiation 1 gene MP:0006095 absent amacrine cells IAGP N RGD:5509061 20141003 MGI PMID:11861467 735545 Neurod1 neurogenic differentiation 1 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:23293286 735545 Neurod1 neurogenic differentiation 1 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18339630 735545 Neurod1 neurogenic differentiation 1 gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23293286 735545 Neurod1 neurogenic differentiation 1 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0008269 abnormal hippocampus CA4 region morphology IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0008285 abnormal hippocampus granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0008285 abnormal hippocampus granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:10804213 735545 Neurod1 neurogenic differentiation 1 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9308961 735545 Neurod1 neurogenic differentiation 1 gene MP:0009161 pancreatic acinar cell zymogen granule accumulation IAGP N RGD:5509061 20141003 MGI PMID:9308961 735545 Neurod1 neurogenic differentiation 1 gene MP:0009173 absent pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:9308961 735545 Neurod1 neurogenic differentiation 1 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:9308961 735545 Neurod1 neurogenic differentiation 1 gene MP:0009181 decreased pancreatic delta cell number IAGP N RGD:5509061 20141003 MGI PMID:9308961 735545 Neurod1 neurogenic differentiation 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:10398678 735545 Neurod1 neurogenic differentiation 1 gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0010802 abnormal intestinal enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9308961 735545 Neurod1 neurogenic differentiation 1 gene MP:0010916 decreased solitary pulmonary neuroendocrine cell number IAGP N RGD:5509061 20141003 MGI PMID:18339630 735545 Neurod1 neurogenic differentiation 1 gene MP:0010919 increased number of pulmonary neuroendocrine bodies IAGP N RGD:5509061 20141003 MGI PMID:18339630 735545 Neurod1 neurogenic differentiation 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10398678 735545 Neurod1 neurogenic differentiation 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10804213 735545 Neurod1 neurogenic differentiation 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9308961 735545 Neurod1 neurogenic differentiation 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10639171 735545 Neurod1 neurogenic differentiation 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15105417 735545 Neurod1 neurogenic differentiation 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16028233 735545 Neurod1 neurogenic differentiation 1 gene MP:0013220 increased pancreas apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9308961 735545 Neurod1 neurogenic differentiation 1 gene MP:0014490 abnormal inner ear vestibular sensory neuron innervation pattern IAGP N RGD:5509061 20240801 MGI PMID:11152640 735545 Neurod1 neurogenic differentiation 1 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:15105417 735548 Gpr19 G protein-coupled receptor 19 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20111116 MGI 735549 Tsx testis specific X-linked gene gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21912526 735549 Tsx testis specific X-linked gene gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:21912526 735549 Tsx testis specific X-linked gene gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21912526 735549 Tsx testis specific X-linked gene gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21912526 735549 Tsx testis specific X-linked gene gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21912526 735551 Sstr4 somatostatin receptor 4 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19622729 735551 Sstr4 somatostatin receptor 4 gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:19622729 735551 Sstr4 somatostatin receptor 4 gene MP:0002441 abnormal granulocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19622729 735551 Sstr4 somatostatin receptor 4 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:19622729 735551 Sstr4 somatostatin receptor 4 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:19622729 735551 Sstr4 somatostatin receptor 4 gene MP:0005407 hyperalgesia IAGP N RGD:5509061 20141003 MGI PMID:19622729 735551 Sstr4 somatostatin receptor 4 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:19622729 735551 Sstr4 somatostatin receptor 4 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:19622729 735551 Sstr4 somatostatin receptor 4 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19622729 735551 Sstr4 somatostatin receptor 4 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:19622729 735551 Sstr4 somatostatin receptor 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 735554 Gmfb glia maturation factor, beta gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15451385 735554 Gmfb glia maturation factor, beta gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:15451385 735554 Gmfb glia maturation factor, beta gene MP:0002807 abnormal eye blink conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15451385 735557 Pde1b phosphodiesterase 1B, Ca2+-calmodulin dependent gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12077213 735557 Pde1b phosphodiesterase 1B, Ca2+-calmodulin dependent gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:12077213 735557 Pde1b phosphodiesterase 1B, Ca2+-calmodulin dependent gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12077213 735557 Pde1b phosphodiesterase 1B, Ca2+-calmodulin dependent gene MP:0003063 increased coping response IEA N RGD:5509061 20111116 MGI 735557 Pde1b phosphodiesterase 1B, Ca2+-calmodulin dependent gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 735557 Pde1b phosphodiesterase 1B, Ca2+-calmodulin dependent gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 735559 Dcbld2 discoidin, CUB and LCCL domain containing 2 gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:24177422 735559 Dcbld2 discoidin, CUB and LCCL domain containing 2 gene MP:0001512 trunk curl IEA N RGD:5509061 20170105 MGI 735559 Dcbld2 discoidin, CUB and LCCL domain containing 2 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:24177422 735559 Dcbld2 discoidin, CUB and LCCL domain containing 2 gene MP:0002833 increased heart weight IEA N RGD:5509061 20160114 MGI 735559 Dcbld2 discoidin, CUB and LCCL domain containing 2 gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24177422 735559 Dcbld2 discoidin, CUB and LCCL domain containing 2 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20201231 MGI 735559 Dcbld2 discoidin, CUB and LCCL domain containing 2 gene MP:0004794 increased anti-nuclear antigen antibody level IEA N RGD:5509061 20201022 MGI 735559 Dcbld2 discoidin, CUB and LCCL domain containing 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:24177422 735559 Dcbld2 discoidin, CUB and LCCL domain containing 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 735559 Dcbld2 discoidin, CUB and LCCL domain containing 2 gene MP:0011134 decreased lung endothelial cell migration IAGP N RGD:5509061 20141003 MGI PMID:24177422 735559 Dcbld2 discoidin, CUB and LCCL domain containing 2 gene MP:0011140 decreased lung endothelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24177422 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20201022 MGI 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20201119 MGI PMID:32492393 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20201119 MGI PMID:32492393 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20201119 MGI PMID:32492393 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20201119 MGI PMID:32492393 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0002715 decreased glycogen catabolism rate IAGP N RGD:5509061 20201119 MGI PMID:32492393 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20170314 MGI PMID:23911327 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20201119 MGI PMID:32492393 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20181227 MGI 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20201119 MGI PMID:32492393 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0004043 abnormal pH regulation IAGP N RGD:5509061 20201119 MGI PMID:32492393 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0005039 hypoxia IAGP N RGD:5509061 20201119 MGI PMID:32492393 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0006057 decreased vascular endothelial cell number IAGP N RGD:5509061 20201119 MGI PMID:32492393 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20201119 MGI PMID:32492393 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15845370 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0012201 decreased endothelial cell proliferation IAGP N RGD:5509061 20170314 MGI PMID:23911327 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0013243 abnormal carbohydrate metabolism IAGP N RGD:5509061 20201119 MGI PMID:32492393 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20201119 MGI PMID:32492393 735561 Pfkfb3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 gene MP:0031126 gangrene IAGP N RGD:5509061 20201119 MGI PMID:32492393 735564 Plce1 phospholipase C, epsilon 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 735564 Plce1 phospholipase C, epsilon 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20210128 MGI 735564 Plce1 phospholipase C, epsilon 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 735564 Plce1 phospholipase C, epsilon 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15743817 735564 Plce1 phospholipase C, epsilon 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 735564 Plce1 phospholipase C, epsilon 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 735564 Plce1 phospholipase C, epsilon 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 735564 Plce1 phospholipase C, epsilon 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15743817 735564 Plce1 phospholipase C, epsilon 1 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15743817 735564 Plce1 phospholipase C, epsilon 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 735564 Plce1 phospholipase C, epsilon 1 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:16293787 735564 Plce1 phospholipase C, epsilon 1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21041529 735564 Plce1 phospholipase C, epsilon 1 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:16293787 735564 Plce1 phospholipase C, epsilon 1 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:23540699 735564 Plce1 phospholipase C, epsilon 1 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15604236 735564 Plce1 phospholipase C, epsilon 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 735564 Plce1 phospholipase C, epsilon 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15743817 735564 Plce1 phospholipase C, epsilon 1 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15743817 735564 Plce1 phospholipase C, epsilon 1 gene MP:0006047 aortic valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:15743817 735564 Plce1 phospholipase C, epsilon 1 gene MP:0006048 pulmonary valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:15743817 735564 Plce1 phospholipase C, epsilon 1 gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:15743817 735564 Plce1 phospholipase C, epsilon 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15604236 735564 Plce1 phospholipase C, epsilon 1 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20220811 MGI 735564 Plce1 phospholipase C, epsilon 1 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20141003 MGI PMID:15743817 735564 Plce1 phospholipase C, epsilon 1 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20141003 MGI PMID:15743817 735564 Plce1 phospholipase C, epsilon 1 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:15743817 735564 Plce1 phospholipase C, epsilon 1 gene MP:0031166 abnormal aortic valve commissure morphology IAGP N RGD:5509061 20210506 MGI PMID:15743817 735564 Plce1 phospholipase C, epsilon 1 gene MP:0031553 abnormal semilunar valve development IAGP N RGD:5509061 20240125 MGI PMID:15743817 735564 Plce1 phospholipase C, epsilon 1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:16293787 735566 Nudc nudC nuclear distribution protein gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20240418 MGI PMID:38441532 735566 Nudc nudC nuclear distribution protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240418 MGI PMID:38441532 735566 Nudc nudC nuclear distribution protein gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20240418 MGI PMID:38441532 735566 Nudc nudC nuclear distribution protein gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20240418 MGI PMID:38441532 735566 Nudc nudC nuclear distribution protein gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20240418 MGI PMID:38441532 735566 Nudc nudC nuclear distribution protein gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20240418 MGI PMID:38441532 735566 Nudc nudC nuclear distribution protein gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20240418 MGI PMID:38441532 735566 Nudc nudC nuclear distribution protein gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20240418 MGI PMID:38441532 735566 Nudc nudC nuclear distribution protein gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20240418 MGI PMID:38441532 735566 Nudc nudC nuclear distribution protein gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20240418 MGI PMID:38441532 735566 Nudc nudC nuclear distribution protein gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20240418 MGI PMID:38441532 735566 Nudc nudC nuclear distribution protein gene MP:0012148 decreased a-wave implicit time IAGP N RGD:5509061 20240418 MGI PMID:38441532 735566 Nudc nudC nuclear distribution protein gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20240418 MGI PMID:38441532 735566 Nudc nudC nuclear distribution protein gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20240418 MGI PMID:38441532 735566 Nudc nudC nuclear distribution protein gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20240418 MGI PMID:38441532 735576 Hk2 hexokinase 2 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20210520 MGI PMID:24280485 735576 Hk2 hexokinase 2 gene MP:0000874 irregular external granule cell layer thickness IAGP N RGD:5509061 20210520 MGI PMID:24280485 735576 Hk2 hexokinase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10428828 735576 Hk2 hexokinase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20210520 MGI PMID:24280485 735576 Hk2 hexokinase 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 735576 Hk2 hexokinase 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20210520 MGI PMID:24280485 735576 Hk2 hexokinase 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10428828 735576 Hk2 hexokinase 2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20210520 MGI PMID:24280485 735576 Hk2 hexokinase 2 gene MP:0006283 increased medulloblastoma incidence IAGP N RGD:5509061 20210520 MGI PMID:24280485 735576 Hk2 hexokinase 2 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20210520 MGI PMID:24280485 735576 Hk2 hexokinase 2 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20210520 MGI PMID:24280485 735576 Hk2 hexokinase 2 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20210520 MGI PMID:24280485 735576 Hk2 hexokinase 2 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10428828 735577 Bag6 BCL2-associated athanogene 6 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0008236 decreased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0010979 small ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0010982 abnormal ureteric bud elongation IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0011032 impaired branching involved in terminal bronchiole morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16287848 735577 Bag6 BCL2-associated athanogene 6 gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16287848 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23133403 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23133403 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23133403 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0002399 abnormal pluripotent precursor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:23133403 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0004029 spontaneous chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:23133403 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0004030 induced chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:23133403 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0010052 increased grip strength IEA N RGD:5509061 20170105 MGI 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0010130 decreased DN1 thymic pro-T cell number IAGP N RGD:5509061 20141003 MGI PMID:23133403 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0010336 increased acute lymphoblastic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:23133403 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23133403 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23133403 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:17143284 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20838603 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 735579 Mcm4 minichromosome maintenance complex component 4 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:15474310 735582 Plcb1 phospholipase C, beta 1 gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20141003 MGI PMID:15474310 735582 Plcb1 phospholipase C, beta 1 gene MP:0000441 increased cranium width IAGP N RGD:5509061 20141003 MGI PMID:15474310 735582 Plcb1 phospholipase C, beta 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210826 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0000771 abnormal brain size IAGP N RGD:5509061 20141003 MGI PMID:15474310 735582 Plcb1 phospholipase C, beta 1 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:9305844 735582 Plcb1 phospholipase C, beta 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210826 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:15474310 735582 Plcb1 phospholipase C, beta 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15474310 735582 Plcb1 phospholipase C, beta 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9305844 735582 Plcb1 phospholipase C, beta 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0001304 cataract IEA N RGD:5509061 20210826 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17667964 735582 Plcb1 phospholipase C, beta 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17667964 735582 Plcb1 phospholipase C, beta 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:17667964 735582 Plcb1 phospholipase C, beta 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15474310 735582 Plcb1 phospholipase C, beta 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15474310 735582 Plcb1 phospholipase C, beta 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15474310 735582 Plcb1 phospholipase C, beta 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220811 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15474310 735582 Plcb1 phospholipase C, beta 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:15474310 735582 Plcb1 phospholipase C, beta 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:9305844 735582 Plcb1 phospholipase C, beta 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:20392936 735582 Plcb1 phospholipase C, beta 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210520 MGI 735582 Plcb1 phospholipase C, beta 1 gene MP:0003240 loss of hippocampal neurons IAGP N RGD:5509061 20141003 MGI PMID:9305844 735582 Plcb1 phospholipase C, beta 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15474310 735582 Plcb1 phospholipase C, beta 1 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:15474310 735582 Plcb1 phospholipase C, beta 1 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15474310 735582 Plcb1 phospholipase C, beta 1 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:17667964 735582 Plcb1 phospholipase C, beta 1 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9305844 735584 Litaf LPS-induced TN factor gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:22729949 735584 Litaf LPS-induced TN factor gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16954198 735584 Litaf LPS-induced TN factor gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20220324 MGI PMID:23576546 735584 Litaf LPS-induced TN factor gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:22729949 735584 Litaf LPS-induced TN factor gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22729949 735584 Litaf LPS-induced TN factor gene MP:0005384 cellular phenotype IAGP N RGD:5509061 20220324 MGI PMID:23576546 735584 Litaf LPS-induced TN factor gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:22729949 735584 Litaf LPS-induced TN factor gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:16954198 735584 Litaf LPS-induced TN factor gene MP:0013147 limb paralysis IAGP N RGD:5509061 20220324 MGI PMID:23576546 735584 Litaf LPS-induced TN factor gene MP:0020848 abnormal exocytosis IAGP N RGD:5509061 20220324 MGI PMID:23576546 735584 Litaf LPS-induced TN factor gene MP:0020851 abnormal vacuole morphology IAGP N RGD:5509061 20220324 MGI PMID:23576546 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:21514445 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:21514445 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:21514445 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0001147 small testis IAGP N RGD:5509061 20161013 MGI PMID:25628439 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20161013 MGI PMID:25628439 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20161013 MGI PMID:25628439 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:21514445 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:21998041 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:21998041 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9770493 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21998041 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9770493 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0001925 male infertility IAGP N RGD:5509061 20161013 MGI PMID:25628439 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9770493 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21998041 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25628439 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20161013 MGI PMID:25628439 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0002662 abnormal cauda epididymis morphology IAGP N RGD:5509061 20161013 MGI PMID:25628439 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21514445 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:21514445 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21514445 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20161013 MGI PMID:25628439 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20161013 MGI PMID:25628439 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9770493 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21998041 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21514445 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21514445 735586 Ppp2ca protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform gene MP:0011243 decreased fetal derived definitive erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:21514445 735588 Ucn urocortin gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12091910 735588 Ucn urocortin gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:12192058 735588 Ucn urocortin gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:12192058 735588 Ucn urocortin gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:17456638 735588 Ucn urocortin gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:17456638 735588 Ucn urocortin gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:12091910 735588 Ucn urocortin gene MP:0004466 short cochlear outer hair cells IAGP N RGD:5509061 20141003 MGI PMID:12091910 735588 Ucn urocortin gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:12091910 735588 Ucn urocortin gene MP:0005345 abnormal circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:17456638 735588 Ucn urocortin gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12091910 735589 Cspg5 chondroitin sulfate proteoglycan 5 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:15848802 735589 Cspg5 chondroitin sulfate proteoglycan 5 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:15848802 735589 Cspg5 chondroitin sulfate proteoglycan 5 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15848802 735589 Cspg5 chondroitin sulfate proteoglycan 5 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:15848802 735589 Cspg5 chondroitin sulfate proteoglycan 5 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15848802 735589 Cspg5 chondroitin sulfate proteoglycan 5 gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:15848802 735590 Uso1 USO1 vesicle docking factor gene MP:0001257 increased body length IEA N RGD:5509061 20230119 MGI 735590 Uso1 USO1 vesicle docking factor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23185636 735590 Uso1 USO1 vesicle docking factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 735590 Uso1 USO1 vesicle docking factor gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20141003 MGI PMID:23185636 735590 Uso1 USO1 vesicle docking factor gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20230119 MGI 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11439183 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:19710169 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20210121 MGI PMID:32882262 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20210121 MGI PMID:32882262 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:11439183 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15057312 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:15057312 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12851457 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:12851457 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12851457 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:12851457 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:11733061 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:11439183 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11439183 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:11439183 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:11439183 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:11733061 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12851457 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0002083 premature death IAGP N RGD:5509061 20210121 MGI PMID:32882262 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12851457 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0002635 reduced sensorimotor gating IAGP N RGD:5509061 20141003 MGI PMID:12851457 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:15057312 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20210121 MGI PMID:32882262 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15057312 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20210121 MGI PMID:32882262 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0003542 abnormal vascular endothelial cell development IAGP N RGD:5509061 20141003 MGI PMID:19710169 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:15057312 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:15057312 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20141003 MGI PMID:15057312 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0004919 abnormal positive T cell selection IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:15057312 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:15057312 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20210121 MGI PMID:32882262 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20210121 MGI PMID:32882262 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0006299 abnormal latent inhibition of conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12851457 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:11733061 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0010563 increased heart right ventricle size IAGP N RGD:5509061 20210121 MGI PMID:32882262 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20210121 MGI PMID:32882262 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11439183 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15030770 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19710169 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0011305 dilated kidney calyx IAGP N RGD:5509061 20141003 MGI PMID:15057312 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0011480 impaired ureteric peristalsis IAGP N RGD:5509061 20141003 MGI PMID:15057312 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0011491 ureteropelvic junction obstruction IAGP N RGD:5509061 20141003 MGI PMID:15057312 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20210121 MGI PMID:32882262 735592 Ppp3r1 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type I) gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:32882262 735593 Cyp4a10 cytochrome P450, family 4, subfamily a, polypeptide 10 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:16691295 735593 Cyp4a10 cytochrome P450, family 4, subfamily a, polypeptide 10 gene MP:0000676 abnormal body water content IAGP N RGD:5509061 20141003 MGI PMID:16691295 735593 Cyp4a10 cytochrome P450, family 4, subfamily a, polypeptide 10 gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:16691295 735593 Cyp4a10 cytochrome P450, family 4, subfamily a, polypeptide 10 gene MP:0004217 salt-sensitive hypertension IAGP N RGD:5509061 20141003 MGI PMID:16691295 735593 Cyp4a10 cytochrome P450, family 4, subfamily a, polypeptide 10 gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:16691295 735593 Cyp4a10 cytochrome P450, family 4, subfamily a, polypeptide 10 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16691295 735593 Cyp4a10 cytochrome P450, family 4, subfamily a, polypeptide 10 gene MP:0010109 abnormal renal sodium reabsorption IAGP N RGD:5509061 20141003 MGI PMID:16691295 735593 Cyp4a10 cytochrome P450, family 4, subfamily a, polypeptide 10 gene MP:0011442 abnormal renal sodium ion transport IAGP N RGD:5509061 20141003 MGI PMID:16691295 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201022 MGI 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:18483067 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20150108 MGI PMID:24719109 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18483067 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20141003 MGI PMID:18483067 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:18483067 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18483067 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20150108 MGI PMID:24719109 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:18483067 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20141003 MGI PMID:19060215 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18483067 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19060215 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18483067 735596 Kcnq3 potassium voltage-gated channel, subfamily Q, member 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18483067 735601 Calcrl calcitonin receptor-like gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:16537897 735601 Calcrl calcitonin receptor-like gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:23635772 735601 Calcrl calcitonin receptor-like gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:18097475 735601 Calcrl calcitonin receptor-like gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:16537897 735601 Calcrl calcitonin receptor-like gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:16537897 735601 Calcrl calcitonin receptor-like gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:16537897 735601 Calcrl calcitonin receptor-like gene MP:0002450 abnormal lymph organ development IAGP N RGD:5509061 20141003 MGI PMID:18097475 735601 Calcrl calcitonin receptor-like gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16537897 735601 Calcrl calcitonin receptor-like gene MP:0003288 intestinal edema IAGP N RGD:5509061 20141003 MGI PMID:16537897 735601 Calcrl calcitonin receptor-like gene MP:0003390 lymphedema IAGP N RGD:5509061 20141003 MGI PMID:18097475 735601 Calcrl calcitonin receptor-like gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16537897 735601 Calcrl calcitonin receptor-like gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16537897 735601 Calcrl calcitonin receptor-like gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16537897 735601 Calcrl calcitonin receptor-like gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:16537897 735601 Calcrl calcitonin receptor-like gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16537897 735601 Calcrl calcitonin receptor-like gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16537897 735601 Calcrl calcitonin receptor-like gene MP:0008876 decreased uterine NK cell number IAGP N RGD:5509061 20141003 MGI PMID:23635772 735601 Calcrl calcitonin receptor-like gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16537897 735601 Calcrl calcitonin receptor-like gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18097475 735601 Calcrl calcitonin receptor-like gene MP:0012727 abnormal uterine spiral artery remodeling IAGP N RGD:5509061 20141003 MGI PMID:23635772 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000030 abnormal tympanic ring morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000088 short mandible IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000168 abnormal bone marrow development IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15986484 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16730346 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:8898212 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:16730346 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:18769073 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20141003 MGI PMID:18769073 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:18769073 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:18769073 735602 Bmp2 bone morphogenetic protein 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:8898212 735602 Bmp2 bone morphogenetic protein 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20181115 MGI PMID:29198724 735602 Bmp2 bone morphogenetic protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18769073 735602 Bmp2 bone morphogenetic protein 2 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16730346 735602 Bmp2 bone morphogenetic protein 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8898212 735602 Bmp2 bone morphogenetic protein 2 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:8898212 735602 Bmp2 bone morphogenetic protein 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:21145505 735602 Bmp2 bone morphogenetic protein 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18769073 735602 Bmp2 bone morphogenetic protein 2 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15986484 735602 Bmp2 bone morphogenetic protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15986484 735602 Bmp2 bone morphogenetic protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0002293 long gestation period IAGP N RGD:5509061 20141003 MGI PMID:18769073 735602 Bmp2 bone morphogenetic protein 2 gene MP:0002639 micrognathia IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:12464426 735602 Bmp2 bone morphogenetic protein 2 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:8898212 735602 Bmp2 bone morphogenetic protein 2 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20181115 MGI PMID:29198724 735602 Bmp2 bone morphogenetic protein 2 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0003854 abnormal forelimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0003856 abnormal hindlimb stylopod morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16314491 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004448 abnormal presphenoid bone morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004458 absent alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004459 small alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004468 small zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004539 absent maxilla IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004558 delayed allantois development IAGP N RGD:5509061 20141003 MGI PMID:8898212 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004574 broad limb buds IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004592 small mandible IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004595 abnormal mandibular condyloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004596 abnormal mandibular angle morphology IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004610 small vertebrae IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004899 absent temporal bone squamous part IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004911 absent mandibular condyloid process IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004912 absent mandibular coronoid process IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004913 absent mandibular angle IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16314491 735602 Bmp2 bone morphogenetic protein 2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:16730346 735602 Bmp2 bone morphogenetic protein 2 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16314491 735602 Bmp2 bone morphogenetic protein 2 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20141003 MGI PMID:8898212 735602 Bmp2 bone morphogenetic protein 2 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16314491 735602 Bmp2 bone morphogenetic protein 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18769073 735602 Bmp2 bone morphogenetic protein 2 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:16314491 735602 Bmp2 bone morphogenetic protein 2 gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0009382 abnormal cardiac jelly morphology IAGP N RGD:5509061 20141003 MGI PMID:16314491 735602 Bmp2 bone morphogenetic protein 2 gene MP:0009874 abnormal interdigital cell death IAGP N RGD:5509061 20141003 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20181115 MGI PMID:29198724 735602 Bmp2 bone morphogenetic protein 2 gene MP:0010224 abnormal heart ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:21145505 735602 Bmp2 bone morphogenetic protein 2 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20181115 MGI PMID:29198724 735602 Bmp2 bone morphogenetic protein 2 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15986484 735602 Bmp2 bone morphogenetic protein 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8898212 735602 Bmp2 bone morphogenetic protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16314491 735602 Bmp2 bone morphogenetic protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16730346 735602 Bmp2 bone morphogenetic protein 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21145505 735602 Bmp2 bone morphogenetic protein 2 gene MP:0011197 abnormal proamniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:8898212 735602 Bmp2 bone morphogenetic protein 2 gene MP:0011495 abnormal head shape IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20063299 735602 Bmp2 bone morphogenetic protein 2 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:8898212 735602 Bmp2 bone morphogenetic protein 2 gene MP:0012270 cardiac edema IAGP N RGD:5509061 20141003 MGI PMID:16730346 735602 Bmp2 bone morphogenetic protein 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20181115 MGI PMID:29198724 735602 Bmp2 bone morphogenetic protein 2 gene MP:0014291 decreased autopod size IAGP N RGD:5509061 20230824 MGI PMID:17194222 735602 Bmp2 bone morphogenetic protein 2 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:23843612 735602 Bmp2 bone morphogenetic protein 2 gene MP:0021213 complete cleft palate IAGP N RGD:5509061 20221201 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0030026 small Meckel's cartilage IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20171005 MGI PMID:22219353 735602 Bmp2 bone morphogenetic protein 2 gene MP:0030261 abnormal temporal bone zygomatic process morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0030302 abnormal maxillary zygomatic process morphology IAGP N RGD:5509061 20221110 MGI PMID:30413887 735602 Bmp2 bone morphogenetic protein 2 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221110 MGI PMID:30413887 735604 Rabggta Rab geranylgeranyl transferase, a subunit gene MP:0000222 decreased neutrophil cell number IEA N RGD:5509061 20211021 MGI 735604 Rabggta Rab geranylgeranyl transferase, a subunit gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:8490171 735604 Rabggta Rab geranylgeranyl transferase, a subunit gene MP:0000371 diluted coat color IEA N RGD:5509061 20111116 MGI 735604 Rabggta Rab geranylgeranyl transferase, a subunit gene MP:0001921 reduced fertility IEA N RGD:5509061 20111116 MGI 735604 Rabggta Rab geranylgeranyl transferase, a subunit gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 735604 Rabggta Rab geranylgeranyl transferase, a subunit gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20141003 MGI PMID:8490171 735604 Rabggta Rab geranylgeranyl transferase, a subunit gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:8490171 735604 Rabggta Rab geranylgeranyl transferase, a subunit gene MP:0004725 decreased platelet serotonin level IAGP N RGD:5509061 20170803 MGI PMID:8490171 735604 Rabggta Rab geranylgeranyl transferase, a subunit gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:11266472 735604 Rabggta Rab geranylgeranyl transferase, a subunit gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20201022 MGI 735604 Rabggta Rab geranylgeranyl transferase, a subunit gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:8490171 735604 Rabggta Rab geranylgeranyl transferase, a subunit gene MP:0014060 abnormal platelet alpha-granule morphology IAGP N RGD:5509061 20170803 MGI PMID:8490171 735604 Rabggta Rab geranylgeranyl transferase, a subunit gene MP:0020432 decreased platelet dense granule number IAGP N RGD:5509061 20170803 MGI PMID:8490171 735604 Rabggta Rab geranylgeranyl transferase, a subunit gene MP:0031165 increased circulating von Willebrand factor level IAGP N RGD:5509061 20201015 MGI PMID:8490171 735607 Ivd isovaleryl coenzyme A dehydrogenase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20160421 MGI 735607 Ivd isovaleryl coenzyme A dehydrogenase gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 735607 Ivd isovaleryl coenzyme A dehydrogenase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735609 Nrg1 neuregulin 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12145742 735609 Nrg1 neuregulin 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:7477375 735609 Nrg1 neuregulin 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9362461 735609 Nrg1 neuregulin 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:9362461 735609 Nrg1 neuregulin 1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:7477375 735609 Nrg1 neuregulin 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7477375 735609 Nrg1 neuregulin 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8643489 735609 Nrg1 neuregulin 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9789034 735609 Nrg1 neuregulin 1 gene MP:0000296 absent trabeculae carneae IAGP N RGD:5509061 20141003 MGI PMID:9362461 735609 Nrg1 neuregulin 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:8643489 735609 Nrg1 neuregulin 1 gene MP:0000299 failure of atrioventricular cushion closure IAGP N RGD:5509061 20141003 MGI PMID:7477375 735609 Nrg1 neuregulin 1 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15044753 735609 Nrg1 neuregulin 1 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11395002 735609 Nrg1 neuregulin 1 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:11395002 735609 Nrg1 neuregulin 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 735609 Nrg1 neuregulin 1 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9637684 735609 Nrg1 neuregulin 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:11395002 735609 Nrg1 neuregulin 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:9110980 735609 Nrg1 neuregulin 1 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:7477375 735609 Nrg1 neuregulin 1 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 735609 Nrg1 neuregulin 1 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9789034 735609 Nrg1 neuregulin 1 gene MP:0001066 absent trigeminal nerve IAGP N RGD:5509061 20141003 MGI PMID:7477375 735609 Nrg1 neuregulin 1 gene MP:0001067 absent mandibular nerve IAGP N RGD:5509061 20141003 MGI PMID:9362461 735609 Nrg1 neuregulin 1 gene MP:0001068 abnormal mandibular nerve branching IAGP N RGD:5509061 20141003 MGI PMID:8643489 735609 Nrg1 neuregulin 1 gene MP:0001068 abnormal mandibular nerve branching IAGP N RGD:5509061 20141003 MGI PMID:9789034 735609 Nrg1 neuregulin 1 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:8643489 735609 Nrg1 neuregulin 1 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:8643489 735609 Nrg1 neuregulin 1 gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 735609 Nrg1 neuregulin 1 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0001080 defasiculated phrenic nerve IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:7477375 735609 Nrg1 neuregulin 1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:8643489 735609 Nrg1 neuregulin 1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 735609 Nrg1 neuregulin 1 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:9789034 735609 Nrg1 neuregulin 1 gene MP:0001084 abnormal petrosal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 735609 Nrg1 neuregulin 1 gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:7477375 735609 Nrg1 neuregulin 1 gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:9789034 735609 Nrg1 neuregulin 1 gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:7477375 735609 Nrg1 neuregulin 1 gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:9362461 735609 Nrg1 neuregulin 1 gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:9789034 735609 Nrg1 neuregulin 1 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8643489 735609 Nrg1 neuregulin 1 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9789034 735609 Nrg1 neuregulin 1 gene MP:0001101 abnormal superior vagus ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:7477375 735609 Nrg1 neuregulin 1 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18760695 735609 Nrg1 neuregulin 1 gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:12495620 735609 Nrg1 neuregulin 1 gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:9342050 735609 Nrg1 neuregulin 1 gene MP:0001108 absent Schwann cells IAGP N RGD:5509061 20141003 MGI PMID:11395002 735609 Nrg1 neuregulin 1 gene MP:0001108 absent Schwann cells IAGP N RGD:5509061 20141003 MGI PMID:12495620 735609 Nrg1 neuregulin 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21715427 735609 Nrg1 neuregulin 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21715427 735609 Nrg1 neuregulin 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15833803 735609 Nrg1 neuregulin 1 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:21949880 735609 Nrg1 neuregulin 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10762692 735609 Nrg1 neuregulin 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12145742 735609 Nrg1 neuregulin 1 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23792428 735609 Nrg1 neuregulin 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23792428 735609 Nrg1 neuregulin 1 gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0001506 limp posture IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15833803 735609 Nrg1 neuregulin 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:9362461 735609 Nrg1 neuregulin 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:7477375 735609 Nrg1 neuregulin 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:9362461 735609 Nrg1 neuregulin 1 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:9789034 735609 Nrg1 neuregulin 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:8643489 735609 Nrg1 neuregulin 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21715427 735609 Nrg1 neuregulin 1 gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:21949880 735609 Nrg1 neuregulin 1 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:15833803 735609 Nrg1 neuregulin 1 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22378872 735609 Nrg1 neuregulin 1 gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:9110980 735609 Nrg1 neuregulin 1 gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20141003 MGI PMID:9110980 735609 Nrg1 neuregulin 1 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:9637684 735609 Nrg1 neuregulin 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22378872 735609 Nrg1 neuregulin 1 gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:12145742 735609 Nrg1 neuregulin 1 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:10762692 735609 Nrg1 neuregulin 1 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:8643489 735609 Nrg1 neuregulin 1 gene MP:0003647 absent oligodendrocytes IAGP N RGD:5509061 20141003 MGI PMID:9892702 735609 Nrg1 neuregulin 1 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:21715427 735609 Nrg1 neuregulin 1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:11395002 735609 Nrg1 neuregulin 1 gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 735609 Nrg1 neuregulin 1 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:12495620 735609 Nrg1 neuregulin 1 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:23792428 735609 Nrg1 neuregulin 1 gene MP:0004075 decreased Schwann cell precursor number IAGP N RGD:5509061 20141003 MGI PMID:7477375 735609 Nrg1 neuregulin 1 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12495620 735609 Nrg1 neuregulin 1 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:9110980 735609 Nrg1 neuregulin 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21715427 735609 Nrg1 neuregulin 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:8643489 735609 Nrg1 neuregulin 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:21715427 735609 Nrg1 neuregulin 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17336907 735609 Nrg1 neuregulin 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17336907 735609 Nrg1 neuregulin 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:8643489 735609 Nrg1 neuregulin 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:9789034 735609 Nrg1 neuregulin 1 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:15044753 735609 Nrg1 neuregulin 1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:12118369 735609 Nrg1 neuregulin 1 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:8643489 735609 Nrg1 neuregulin 1 gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21715427 735609 Nrg1 neuregulin 1 gene MP:0008486 decreased muscle spindle number IAGP N RGD:5509061 20141003 MGI PMID:23792428 735609 Nrg1 neuregulin 1 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15833803 735609 Nrg1 neuregulin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10707974 735609 Nrg1 neuregulin 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11395002 735609 Nrg1 neuregulin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12145742 735609 Nrg1 neuregulin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7477375 735609 Nrg1 neuregulin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8643489 735609 Nrg1 neuregulin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9362461 735609 Nrg1 neuregulin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9789034 735609 Nrg1 neuregulin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 735609 Nrg1 neuregulin 1 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21949880 735609 Nrg1 neuregulin 1 gene MP:0014119 abnormal mandibular nerve innervation pattern IAGP N RGD:5509061 20160414 MGI PMID:7477375 735609 Nrg1 neuregulin 1 gene MP:0020388 decreased radial glial cell number IAGP N RGD:5509061 20161117 MGI PMID:12649319 735609 Nrg1 neuregulin 1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15833803 735614 Mta1 metastasis associated 1 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20141003 MGI 735614 Mta1 metastasis associated 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20160804 MGI 735614 Mta1 metastasis associated 1 gene MP:0001539 decreased caudal vertebrae number IEA N RGD:5509061 20141003 MGI 735614 Mta1 metastasis associated 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 735614 Mta1 metastasis associated 1 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 735614 Mta1 metastasis associated 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20160804 MGI 735614 Mta1 metastasis associated 1 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:19805145 735614 Mta1 metastasis associated 1 gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20141003 MGI 735614 Mta1 metastasis associated 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 735614 Mta1 metastasis associated 1 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:17666527 735614 Mta1 metastasis associated 1 gene MP:0010101 increased sacral vertebrae number IEA N RGD:5509061 20141003 MGI 735622 Gdf15 growth differentiation factor 15 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23468844 735622 Gdf15 growth differentiation factor 15 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19864576 735622 Gdf15 growth differentiation factor 15 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:19864576 735622 Gdf15 growth differentiation factor 15 gene MP:0001019 abnormal L4 dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:19864576 735622 Gdf15 growth differentiation factor 15 gene MP:0001022 abnormal L5 dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:19864576 735622 Gdf15 growth differentiation factor 15 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19864576 735622 Gdf15 growth differentiation factor 15 gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:19864576 735622 Gdf15 growth differentiation factor 15 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19864576 735622 Gdf15 growth differentiation factor 15 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23468844 735622 Gdf15 growth differentiation factor 15 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23468844 735622 Gdf15 growth differentiation factor 15 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19864576 735622 Gdf15 growth differentiation factor 15 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0002752 abnormal somatic nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:19864576 735622 Gdf15 growth differentiation factor 15 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:16397141 735622 Gdf15 growth differentiation factor 15 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23468844 735622 Gdf15 growth differentiation factor 15 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:23468844 735622 Gdf15 growth differentiation factor 15 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:23231375 735622 Gdf15 growth differentiation factor 15 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:19864576 735622 Gdf15 growth differentiation factor 15 gene MP:0008961 abnormal basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:23468844 735622 Gdf15 growth differentiation factor 15 gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23468844 735622 Gdf15 growth differentiation factor 15 gene MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23468844 735622 Gdf15 growth differentiation factor 15 gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:23468844 735622 Gdf15 growth differentiation factor 15 gene MP:0009586 increased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:23231375 735622 Gdf15 growth differentiation factor 15 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23231375 735622 Gdf15 growth differentiation factor 15 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23468844 735622 Gdf15 growth differentiation factor 15 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:23468844 735622 Gdf15 growth differentiation factor 15 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:23986522 735622 Gdf15 growth differentiation factor 15 gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:23231375 735630 Amigo3 adhesion molecule with Ig like domain 3 gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:18174359 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:22962254 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:18174359 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0000646 enlarged adrenocortical cells IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0001159 absent prostate gland IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:22962254 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0001776 abnormal circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:18174359 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0002668 abnormal circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0002670 absent scrotum IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0002770 absent bulbourethral gland IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0002771 absent prostate gland anterior lobe IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0002909 abnormal adrenal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:18174359 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0003253 dilated bile duct IEA N RGD:5509061 20170504 MGI 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:22962254 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20170504 MGI 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0004933 abnormal epididymis epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0005244 hemopericardium IEA N RGD:5509061 20170504 MGI 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:18174359 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:18174359 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:22962254 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18174359 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18174359 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0008291 abnormal adrenocortical cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22962254 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0008293 abnormal adrenal gland zona glomerulosa morphology IAGP N RGD:5509061 20141003 MGI PMID:18174359 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0008294 abnormal adrenal gland zona fasciculata morphology IAGP N RGD:5509061 20141003 MGI PMID:18174359 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0008505 absent adrenal chromaffin cells IAGP N RGD:5509061 20141003 MGI PMID:22962254 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18174359 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22962254 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20200716 MGI PMID:12145347 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:22962254 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20170504 MGI 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0014087 retrolental blood IEA N RGD:5509061 20180628 MGI 735632 Cyp11a1 cytochrome P450, family 11, subfamily a, polypeptide 1 gene MP:0030762 decreased adrenaline level IAGP N RGD:5509061 20180927 MGI PMID:22962254 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11733567 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20160128 MGI PMID:15342683 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0000184 abnormal circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9539787 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18772481 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11861300 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20220120 MGI PMID:25368174 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:11861300 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0000256 echinocytosis IAGP N RGD:5509061 20141003 MGI PMID:11861300 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:24082102 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20190502 MGI 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:19654867 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20190502 MGI 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10430941 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:19654867 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19654867 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12006675 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:14993241 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16964311 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18772481 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19654867 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9539787 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20160128 MGI PMID:15342683 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:11861300 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10430941 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11733567 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:16964311 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20220120 MGI PMID:25368174 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24082102 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10430941 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9356497 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9539787 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11861300 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:11861300 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:11861300 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20181227 MGI 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:24082102 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:11861300 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0002909 abnormal adrenal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:9356497 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0003191 abnormal cellular cholesterol metabolism IAGP N RGD:5509061 20220120 MGI PMID:25368174 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0003406 failure of zygotic cell division IAGP N RGD:5509061 20141003 MGI PMID:10430941 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0003947 abnormal cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9356497 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0003980 increased circulating phospholipid level IAGP N RGD:5509061 20141003 MGI PMID:19654867 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0003982 increased cholesterol level IAGP N RGD:5509061 20220120 MGI PMID:25368174 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:24082102 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20201022 MGI 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:16339487 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20220811 MGI 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20220120 MGI PMID:25368174 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16964311 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19654867 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9356497 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20160128 MGI PMID:15342683 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20240627 MGI PMID:9539787 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19654867 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210128 MGI 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:10764675 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:24082102 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16964311 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20211021 MGI 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0006134 artery occlusion IAGP N RGD:5509061 20141003 MGI PMID:24082102 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0008389 hypochromic macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:11861300 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:16964311 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0009093 oocyte degeneration IAGP N RGD:5509061 20220120 MGI PMID:25368174 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0010570 prolonged ST segment IEA N RGD:5509061 20211021 MGI 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10430941 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0011953 prolonged PQ interval IEA N RGD:5509061 20211021 MGI 735634 Scarb1 scavenger receptor class B, member 1 gene MP:0031013 abnormal egg activation IAGP N RGD:5509061 20220120 MGI PMID:25368174 735636 Prodh proline dehydrogenase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10192398 735636 Prodh proline dehydrogenase gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:10192398 735636 Prodh proline dehydrogenase gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20230601 MGI 735636 Prodh proline dehydrogenase gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20230601 MGI 735636 Prodh proline dehydrogenase gene MP:0002764 short tibia IEA N RGD:5509061 20160114 MGI 735636 Prodh proline dehydrogenase gene MP:0020237 increased proline level IAGP N RGD:5509061 20180927 MGI PMID:10192398 735636 Prodh proline dehydrogenase gene MP:0030667 increased circulating proline level IAGP N RGD:5509061 20180927 MGI PMID:10192398 735636 Prodh proline dehydrogenase gene MP:0030733 decreased gamma-aminobutyric acid level IAGP N RGD:5509061 20180927 MGI PMID:10192398 735636 Prodh proline dehydrogenase gene MP:0030737 decreased glutamic acid level IAGP N RGD:5509061 20180927 MGI PMID:10192398 735636 Prodh proline dehydrogenase gene MP:0030743 decreased aspartic acid level IAGP N RGD:5509061 20180927 MGI PMID:10192398 735640 Qpct glutaminyl-peptide cyclotransferase (glutaminyl cyclase) gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20230323 MGI PMID:35314846 735640 Qpct glutaminyl-peptide cyclotransferase (glutaminyl cyclase) gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:21148560 735640 Qpct glutaminyl-peptide cyclotransferase (glutaminyl cyclase) gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:21900558 735644 Pdzd2 PDZ domain containing 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20210722 MGI PMID:19932150 735644 Pdzd2 PDZ domain containing 2 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20210722 MGI PMID:19932150 735644 Pdzd2 PDZ domain containing 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20210722 MGI PMID:19932150 735644 Pdzd2 PDZ domain containing 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20210722 MGI PMID:19932150 735646 Braf Braf transforming gene gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0000097 short maxilla IAGP N RGD:5509061 20150910 MGI PMID:18952847 735646 Braf Braf transforming gene gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0000160 kyphosis IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0000160 kyphosis IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16357158 735646 Braf Braf transforming gene gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16357158 735646 Braf Braf transforming gene gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0000274 enlarged heart IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0000274 enlarged heart IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0000275 heart hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20150910 MGI PMID:18952847 735646 Braf Braf transforming gene gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16357158 735646 Braf Braf transforming gene gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21514245 735646 Braf Braf transforming gene gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0000416 sparse hair IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0000420 ruffled hair IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0000432 abnormal head morphology IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0000435 shortened head IAGP N RGD:5509061 20171019 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20150910 MGI PMID:18952847 735646 Braf Braf transforming gene gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0000562 polydactyly IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16357158 735646 Braf Braf transforming gene gene MP:0000601 small liver IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20150910 MGI PMID:18952847 735646 Braf Braf transforming gene gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20160721 MGI PMID:21512141 735646 Braf Braf transforming gene gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16357158 735646 Braf Braf transforming gene gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20180830 MGI PMID:24638167 735646 Braf Braf transforming gene gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0000706 small thymus IAGP N RGD:5509061 20150910 MGI PMID:18952847 735646 Braf Braf transforming gene gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16980614 735646 Braf Braf transforming gene gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16980614 735646 Braf Braf transforming gene gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16980614 735646 Braf Braf transforming gene gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:16980614 735646 Braf Braf transforming gene gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:24216512 735646 Braf Braf transforming gene gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:17299132 735646 Braf Braf transforming gene gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:19345328 735646 Braf Braf transforming gene gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:20141835 735646 Braf Braf transforming gene gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:19345328 735646 Braf Braf transforming gene gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:22796458 735646 Braf Braf transforming gene gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:24216512 735646 Braf Braf transforming gene gene MP:0001212 skin lesions IAGP N RGD:5509061 20170622 MGI PMID:19282848 735646 Braf Braf transforming gene gene MP:0001255 decreased body height IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16980614 735646 Braf Braf transforming gene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160714 MGI PMID:21220306 735646 Braf Braf transforming gene gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22836754 735646 Braf Braf transforming gene gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20170608 MGI PMID:24711431 735646 Braf Braf transforming gene gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20170622 MGI PMID:19282848 735646 Braf Braf transforming gene gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0001377 abnormal mating frequency IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:24216512 735646 Braf Braf transforming gene gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16342120 735646 Braf Braf transforming gene gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16342120 735646 Braf Braf transforming gene gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0001575 cyanosis IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0001577 anemia IAGP N RGD:5509061 20180830 MGI PMID:24638167 735646 Braf Braf transforming gene gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16432225 735646 Braf Braf transforming gene gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:16980614 735646 Braf Braf transforming gene gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:16432225 735646 Braf Braf transforming gene gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:16432225 735646 Braf Braf transforming gene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16432225 735646 Braf Braf transforming gene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0001785 edema IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20180830 MGI PMID:24638167 735646 Braf Braf transforming gene gene MP:0001860 liver inflammation IAGP N RGD:5509061 20180830 MGI PMID:24638167 735646 Braf Braf transforming gene gene MP:0001861 lung inflammation IAGP N RGD:5509061 20180830 MGI PMID:24638167 735646 Braf Braf transforming gene gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0001914 hemorrhage IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0001926 female infertility IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0001953 respiratory failure IAGP N RGD:5509061 20170608 MGI PMID:24711431 735646 Braf Braf transforming gene gene MP:0002016 ovary cyst IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20141835 735646 Braf Braf transforming gene gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:16357158 735646 Braf Braf transforming gene gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17299132 735646 Braf Braf transforming gene gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17299132 735646 Braf Braf transforming gene gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:16342120 735646 Braf Braf transforming gene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16357158 735646 Braf Braf transforming gene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16980614 735646 Braf Braf transforming gene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17299132 735646 Braf Braf transforming gene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21514245 735646 Braf Braf transforming gene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22796458 735646 Braf Braf transforming gene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22836754 735646 Braf Braf transforming gene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0002083 premature death IAGP N RGD:5509061 20170608 MGI PMID:24711431 735646 Braf Braf transforming gene gene MP:0002083 premature death IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0002083 premature death IAGP N RGD:5509061 20180830 MGI PMID:24638167 735646 Braf Braf transforming gene gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16432225 735646 Braf Braf transforming gene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17299132 735646 Braf Braf transforming gene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21514245 735646 Braf Braf transforming gene gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:24216512 735646 Braf Braf transforming gene gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:24216512 735646 Braf Braf transforming gene gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0002450 abnormal lymph organ development IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20180830 MGI PMID:24638167 735646 Braf Braf transforming gene gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20150910 MGI PMID:18952847 735646 Braf Braf transforming gene gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0002833 increased heart weight IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16357158 735646 Braf Braf transforming gene gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20170622 MGI PMID:19282848 735646 Braf Braf transforming gene gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20150910 MGI PMID:18952847 735646 Braf Braf transforming gene gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20160714 MGI PMID:21220306 735646 Braf Braf transforming gene gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0003057 abnormal epicardium morphology IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20160714 MGI PMID:21220306 735646 Braf Braf transforming gene gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20160721 MGI PMID:21512141 735646 Braf Braf transforming gene gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0003968 abnormal growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0004163 abnormal adenohypophysis morphology IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0004225 patent cardiac foramen ovale IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16432225 735646 Braf Braf transforming gene gene MP:0004259 small placenta IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:19345328 735646 Braf Braf transforming gene gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20160714 MGI PMID:21220306 735646 Braf Braf transforming gene gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20160721 MGI PMID:21512141 735646 Braf Braf transforming gene gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:24216512 735646 Braf Braf transforming gene gene MP:0004831 long incisors IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16980614 735646 Braf Braf transforming gene gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:16980614 735646 Braf Braf transforming gene gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16432225 735646 Braf Braf transforming gene gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20160714 MGI PMID:21220306 735646 Braf Braf transforming gene gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20160721 MGI PMID:21512141 735646 Braf Braf transforming gene gene MP:0005135 increased thyroid-stimulating hormone level IAGP N RGD:5509061 20170608 MGI PMID:24711431 735646 Braf Braf transforming gene gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20160721 MGI PMID:21512141 735646 Braf Braf transforming gene gene MP:0005426 tachypnea IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20160714 MGI PMID:21220306 735646 Braf Braf transforming gene gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20160721 MGI PMID:21512141 735646 Braf Braf transforming gene gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0005577 uterus prolapse IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0005621 abnormal cell physiology IEA N RGD:5509061 20211118 MGI 735646 Braf Braf transforming gene gene MP:0005655 increased aggression IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0005665 increased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16980614 735646 Braf Braf transforming gene gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:16980614 735646 Braf Braf transforming gene gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17299132 735646 Braf Braf transforming gene gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20180830 MGI PMID:24638167 735646 Braf Braf transforming gene gene MP:0008256 abnormal myometrium morphology IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0008285 abnormal hippocampus granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0008321 small adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0008716 increased lung non-small cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21514245 735646 Braf Braf transforming gene gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:16432225 735646 Braf Braf transforming gene gene MP:0008817 hematoma IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:22836754 735646 Braf Braf transforming gene gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22836754 735646 Braf Braf transforming gene gene MP:0009322 increased splenocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0009386 abnormal dermal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0009535 abnormal skin sebaceous gland morphology IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20160721 MGI PMID:21512141 735646 Braf Braf transforming gene gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:24216512 735646 Braf Braf transforming gene gene MP:0009957 abnormal cerebellum vermis lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16980614 735646 Braf Braf transforming gene gene MP:0009988 abnormal cerebellum vermis lobule I morphology IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0009989 abnormal cerebellum vermis lobule II morphology IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0009990 abnormal cerebellum vermis lobule III morphology IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0009993 abnormal cerebellum vermis lobule V morphology IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0009995 abnormal cerebellum vermis lobule VII morphology IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0009997 abnormal cerebellum vermis lobule X morphology IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19345328 735646 Braf Braf transforming gene gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20141835 735646 Braf Braf transforming gene gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22000016 735646 Braf Braf transforming gene gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20200402 MGI PMID:27135738 735646 Braf Braf transforming gene gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0010288 increased gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19345328 735646 Braf Braf transforming gene gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20160714 MGI PMID:21220306 735646 Braf Braf transforming gene gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22796458 735646 Braf Braf transforming gene gene MP:0010322 increased cutaneous melanoma incidence IAGP N RGD:5509061 20170622 MGI PMID:19282848 735646 Braf Braf transforming gene gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20160714 MGI PMID:21220306 735646 Braf Braf transforming gene gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20160721 MGI PMID:21512141 735646 Braf Braf transforming gene gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20170608 MGI PMID:24711431 735646 Braf Braf transforming gene gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22836754 735646 Braf Braf transforming gene gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20150910 MGI PMID:18952847 735646 Braf Braf transforming gene gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0010405 ostium secundum atrial septal defect IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0010583 abnormal conotruncus morphology IAGP N RGD:5509061 20150910 MGI PMID:18952847 735646 Braf Braf transforming gene gene MP:0010600 enlarged pulmonary valve IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0010602 abnormal pulmonary valve cusp morphology IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0010605 thick pulmonary valve cusps IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0010617 thick mitral valve cusps IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0010629 thick tricuspid valve IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20141003 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0010909 pulmonary alveolar hemorrhage IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0010945 lung epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17299132 735646 Braf Braf transforming gene gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16432225 735646 Braf Braf transforming gene gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16357158 735646 Braf Braf transforming gene gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16432225 735646 Braf Braf transforming gene gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16980614 735646 Braf Braf transforming gene gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17396120 735646 Braf Braf transforming gene gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9207797 735646 Braf Braf transforming gene gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20150910 MGI PMID:18952847 735646 Braf Braf transforming gene gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16980614 735646 Braf Braf transforming gene gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20170622 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0011276 increased tail pigmentation IEA N RGD:5509061 20211118 MGI 735646 Braf Braf transforming gene gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:22892241 735646 Braf Braf transforming gene gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:16357158 735646 Braf Braf transforming gene gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0011940 decreased food intake IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0012400 nail dystrophy IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0012401 long nails IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0013957 increased small intestine length IAGP N RGD:5509061 20160310 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0013959 increased large intestine length IAGP N RGD:5509061 20160310 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0014081 branched small intestinal villi IAGP N RGD:5509061 20160310 MGI PMID:23845441 735646 Braf Braf transforming gene gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:22796458 735646 Braf Braf transforming gene gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:24711431 735646 Braf Braf transforming gene gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:21203559 735646 Braf Braf transforming gene gene MP:0020393 increased neuronal precursor proliferation IAGP N RGD:5509061 20161117 MGI PMID:23505473 735646 Braf Braf transforming gene gene MP:0030245 round head IAGP N RGD:5509061 20171019 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0030245 round head IAGP N RGD:5509061 20180719 MGI PMID:26472072 735646 Braf Braf transforming gene gene MP:0031058 hepatosplenomegaly IAGP N RGD:5509061 20200618 MGI PMID:24638167 735646 Braf Braf transforming gene gene MP:0031066 cytokine storm IAGP N RGD:5509061 20200618 MGI PMID:24638167 735646 Braf Braf transforming gene gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:21383153 735646 Braf Braf transforming gene gene MP:0031559 tricuspid valve hypertrophy IAGP N RGD:5509061 20240104 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0031563 pulmonary valve hypertrophy IAGP N RGD:5509061 20240125 MGI PMID:25035421 735646 Braf Braf transforming gene gene MP:0031564 mitral valve hypertrophy IAGP N RGD:5509061 20240125 MGI PMID:25035421 735647 Smad3 SMAD family member 3 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0000069 kyphoscoliosis IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:10082515 735647 Smad3 SMAD family member 3 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:10082515 735647 Smad3 SMAD family member 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10082515 735647 Smad3 SMAD family member 3 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12842913 735647 Smad3 SMAD family member 3 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10082515 735647 Smad3 SMAD family member 3 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16382155 735647 Smad3 SMAD family member 3 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:9753318 735647 Smad3 SMAD family member 3 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:11438667 735647 Smad3 SMAD family member 3 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20220428 MGI PMID:11906909 735647 Smad3 SMAD family member 3 gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:20197623 735647 Smad3 SMAD family member 3 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:9753318 735647 Smad3 SMAD family member 3 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:20197623 735647 Smad3 SMAD family member 3 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10082515 735647 Smad3 SMAD family member 3 gene MP:0000597 delayed hepatic development IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11438667 735647 Smad3 SMAD family member 3 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11438667 735647 Smad3 SMAD family member 3 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:11438667 735647 Smad3 SMAD family member 3 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:11438667 735647 Smad3 SMAD family member 3 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0000997 abnormal synovial joint capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220428 MGI PMID:11906909 735647 Smad3 SMAD family member 3 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:17652186 735647 Smad3 SMAD family member 3 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18809571 735647 Smad3 SMAD family member 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:17804483 735647 Smad3 SMAD family member 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220428 MGI PMID:11906909 735647 Smad3 SMAD family member 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10082515 735647 Smad3 SMAD family member 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9753318 735647 Smad3 SMAD family member 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220428 MGI PMID:11906909 735647 Smad3 SMAD family member 3 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:9753318 735647 Smad3 SMAD family member 3 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:9753318 735647 Smad3 SMAD family member 3 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:9753318 735647 Smad3 SMAD family member 3 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:18809571 735647 Smad3 SMAD family member 3 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:18809571 735647 Smad3 SMAD family member 3 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16424015 735647 Smad3 SMAD family member 3 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:18809571 735647 Smad3 SMAD family member 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220428 MGI PMID:11906909 735647 Smad3 SMAD family member 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18809571 735647 Smad3 SMAD family member 3 gene MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17652186 735647 Smad3 SMAD family member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16382155 735647 Smad3 SMAD family member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9753318 735647 Smad3 SMAD family member 3 gene MP:0002083 premature death IAGP N RGD:5509061 20220428 MGI PMID:11906909 735647 Smad3 SMAD family member 3 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:20508035 735647 Smad3 SMAD family member 3 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:9753318 735647 Smad3 SMAD family member 3 gene MP:0002230 abnormal primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:20508035 735647 Smad3 SMAD family member 3 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10559937 735647 Smad3 SMAD family member 3 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:10559937 735647 Smad3 SMAD family member 3 gene MP:0002776 increased Sertoli cell number IAGP N RGD:5509061 20220630 MGI PMID:17652186 735647 Smad3 SMAD family member 3 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16424015 735647 Smad3 SMAD family member 3 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:9753318 735647 Smad3 SMAD family member 3 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20230119 MGI 735647 Smad3 SMAD family member 3 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:10082515 735647 Smad3 SMAD family member 3 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:21525133 735647 Smad3 SMAD family member 3 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11438667 735647 Smad3 SMAD family member 3 gene MP:0003200 calcified joint IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15253712 735647 Smad3 SMAD family member 3 gene MP:0003269 colon polyps IAGP N RGD:5509061 20141003 MGI PMID:20197623 735647 Smad3 SMAD family member 3 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:9753318 735647 Smad3 SMAD family member 3 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10559937 735647 Smad3 SMAD family member 3 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:15630024 735647 Smad3 SMAD family member 3 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:17804483 735647 Smad3 SMAD family member 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11438667 735647 Smad3 SMAD family member 3 gene MP:0004041 increased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:18434384 735647 Smad3 SMAD family member 3 gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:21525133 735647 Smad3 SMAD family member 3 gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:18434384 735647 Smad3 SMAD family member 3 gene MP:0004199 increased fetal size IAGP N RGD:5509061 20141003 MGI PMID:11438667 735647 Smad3 SMAD family member 3 gene MP:0004387 abnormal prechordal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20508035 735647 Smad3 SMAD family member 3 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:10082515 735647 Smad3 SMAD family member 3 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:15790953 735647 Smad3 SMAD family member 3 gene MP:0004967 abnormal kidney epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14617750 735647 Smad3 SMAD family member 3 gene MP:0005094 abnormal T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10082515 735647 Smad3 SMAD family member 3 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0005109 abnormal talus morphology IAGP N RGD:5509061 20141003 MGI PMID:10082515 735647 Smad3 SMAD family member 3 gene MP:0005153 abnormal B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10082515 735647 Smad3 SMAD family member 3 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:20508035 735647 Smad3 SMAD family member 3 gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:14617750 735647 Smad3 SMAD family member 3 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:15253712 735647 Smad3 SMAD family member 3 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:9753318 735647 Smad3 SMAD family member 3 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:18809571 735647 Smad3 SMAD family member 3 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:18434384 735647 Smad3 SMAD family member 3 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:17804483 735647 Smad3 SMAD family member 3 gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:21525133 735647 Smad3 SMAD family member 3 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17804483 735647 Smad3 SMAD family member 3 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:21525133 735647 Smad3 SMAD family member 3 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11984875 735647 Smad3 SMAD family member 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16382155 735647 Smad3 SMAD family member 3 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16382155 735647 Smad3 SMAD family member 3 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11285272 735647 Smad3 SMAD family member 3 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17652186 735647 Smad3 SMAD family member 3 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18474630 735647 Smad3 SMAD family member 3 gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0008595 abnormal circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:21525133 735647 Smad3 SMAD family member 3 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21525133 735647 Smad3 SMAD family member 3 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:10064594 735647 Smad3 SMAD family member 3 gene MP:0008783 decreased B cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18704116 735647 Smad3 SMAD family member 3 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17804483 735647 Smad3 SMAD family member 3 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18434384 735647 Smad3 SMAD family member 3 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16382155 735647 Smad3 SMAD family member 3 gene MP:0008926 abnormal anterior definitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:20508035 735647 Smad3 SMAD family member 3 gene MP:0009266 abnormal mesendoderm development IAGP N RGD:5509061 20141003 MGI PMID:20508035 735647 Smad3 SMAD family member 3 gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20197623 735647 Smad3 SMAD family member 3 gene MP:0009373 abnormal cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:18809571 735647 Smad3 SMAD family member 3 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11438667 735647 Smad3 SMAD family member 3 gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16041381 735647 Smad3 SMAD family member 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 735647 Smad3 SMAD family member 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11438667 735647 Smad3 SMAD family member 3 gene MP:0011120 increased primordial ovarian follicle number IAGP N RGD:5509061 20220428 MGI PMID:11906909 735647 Smad3 SMAD family member 3 gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220428 MGI PMID:11906909 735647 Smad3 SMAD family member 3 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18809571 735647 Smad3 SMAD family member 3 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220428 MGI PMID:11906909 735647 Smad3 SMAD family member 3 gene MP:0011338 abnormal mesangial matrix morphology IAGP N RGD:5509061 20141003 MGI PMID:17804483 735647 Smad3 SMAD family member 3 gene MP:0011349 abnormal renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:17804483 735647 Smad3 SMAD family member 3 gene MP:0011372 decreased renal tubule apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15253712 735647 Smad3 SMAD family member 3 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:15253712 735647 Smad3 SMAD family member 3 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:12842913 735647 Smad3 SMAD family member 3 gene MP:0012083 absent foregut IAGP N RGD:5509061 20141003 MGI PMID:12842913 735647 Smad3 SMAD family member 3 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:12842913 735647 Smad3 SMAD family member 3 gene MP:0012245 abnormal hepatoblast migration IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0012246 abnormal hepatic cord morphology IAGP N RGD:5509061 20141003 MGI PMID:11438667 735647 Smad3 SMAD family member 3 gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:15183723 735647 Smad3 SMAD family member 3 gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20200130 MGI PMID:18809571 735647 Smad3 SMAD family member 3 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18809571 735647 Smad3 SMAD family member 3 gene MP:0031381 decreased secondary ovarian follicle number IAGP N RGD:5509061 20220428 MGI PMID:11906909 735649 Tef thyrotroph embryonic factor gene MP:0000599 enlarged liver IAGP N RGD:5509061 20180705 MGI PMID:16814730 735649 Tef thyrotroph embryonic factor gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:15175240 735649 Tef thyrotroph embryonic factor gene MP:0001596 hypotension IAGP N RGD:5509061 20180705 MGI PMID:20686175 735649 Tef thyrotroph embryonic factor gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20180705 MGI PMID:20686175 735649 Tef thyrotroph embryonic factor gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15175240 735649 Tef thyrotroph embryonic factor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15175240 735649 Tef thyrotroph embryonic factor gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15175240 735649 Tef thyrotroph embryonic factor gene MP:0002667 decreased circulating aldosterone level IAGP N RGD:5509061 20180705 MGI PMID:20686175 735649 Tef thyrotroph embryonic factor gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20180705 MGI PMID:16814730 735649 Tef thyrotroph embryonic factor gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:15175240 735649 Tef thyrotroph embryonic factor gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:15175240 735649 Tef thyrotroph embryonic factor gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:15175240 735649 Tef thyrotroph embryonic factor gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20180920 MGI PMID:15175240 735649 Tef thyrotroph embryonic factor gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180705 MGI PMID:16814730 735649 Tef thyrotroph embryonic factor gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20180705 MGI PMID:16814730 735649 Tef thyrotroph embryonic factor gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:15175240 735651 Gata6 GATA binding protein 6 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:24380800 735651 Gata6 GATA binding protein 6 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:16557299 735651 Gata6 GATA binding protein 6 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:24380800 735651 Gata6 GATA binding protein 6 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:24415953 735651 Gata6 GATA binding protein 6 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17142311 735651 Gata6 GATA binding protein 6 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17164424 735651 Gata6 GATA binding protein 6 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:16557299 735651 Gata6 GATA binding protein 6 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:9832509 735651 Gata6 GATA binding protein 6 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:9895320 735651 Gata6 GATA binding protein 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15767668 735651 Gata6 GATA binding protein 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9832509 735651 Gata6 GATA binding protein 6 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20160128 MGI PMID:26498761 735651 Gata6 GATA binding protein 6 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:16557299 735651 Gata6 GATA binding protein 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16611361 735651 Gata6 GATA binding protein 6 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16557299 735651 Gata6 GATA binding protein 6 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:24380800 735651 Gata6 GATA binding protein 6 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:24380800 735651 Gata6 GATA binding protein 6 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9832509 735651 Gata6 GATA binding protein 6 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20141003 MGI PMID:16557299 735651 Gata6 GATA binding protein 6 gene MP:0004160 retroesophageal right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:16557299 735651 Gata6 GATA binding protein 6 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17164424 735651 Gata6 GATA binding protein 6 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18400219 735651 Gata6 GATA binding protein 6 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:24415953 735651 Gata6 GATA binding protein 6 gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16557299 735651 Gata6 GATA binding protein 6 gene MP:0010485 aortic arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16557299 735651 Gata6 GATA binding protein 6 gene MP:0010485 aortic arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0010541 aorta hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0010545 abnormal heart layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24380800 735651 Gata6 GATA binding protein 6 gene MP:0010565 absent fetal ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16557299 735651 Gata6 GATA binding protein 6 gene MP:0010574 dilated aorta IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0010814 absent alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:17164424 735651 Gata6 GATA binding protein 6 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:17164424 735651 Gata6 GATA binding protein 6 gene MP:0010898 abnormal pulmonary alveolus epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17164424 735651 Gata6 GATA binding protein 6 gene MP:0010993 decreased surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:17164424 735651 Gata6 GATA binding protein 6 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17164424 735651 Gata6 GATA binding protein 6 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16557299 735651 Gata6 GATA binding protein 6 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16611361 735651 Gata6 GATA binding protein 6 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9832509 735651 Gata6 GATA binding protein 6 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9895320 735651 Gata6 GATA binding protein 6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15767668 735651 Gata6 GATA binding protein 6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16611361 735651 Gata6 GATA binding protein 6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24380800 735651 Gata6 GATA binding protein 6 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20160128 MGI PMID:26498761 735651 Gata6 GATA binding protein 6 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24380800 735651 Gata6 GATA binding protein 6 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:17164424 735651 Gata6 GATA binding protein 6 gene MP:0011183 abnormal primitive endoderm morphology IAGP N RGD:5509061 20160728 MGI PMID:25209243 735651 Gata6 GATA binding protein 6 gene MP:0011185 absent primitive endoderm IAGP N RGD:5509061 20160728 MGI PMID:24835466 735651 Gata6 GATA binding protein 6 gene MP:0011185 absent primitive endoderm IAGP N RGD:5509061 20160728 MGI PMID:25209243 735651 Gata6 GATA binding protein 6 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:16847256 735651 Gata6 GATA binding protein 6 gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:9832509 735651 Gata6 GATA binding protein 6 gene MP:0011191 increased embryonic epiblast cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9832509 735651 Gata6 GATA binding protein 6 gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:18400219 735651 Gata6 GATA binding protein 6 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:24380800 735651 Gata6 GATA binding protein 6 gene MP:0012081 absent heart tube IAGP N RGD:5509061 20141003 MGI PMID:18400219 735651 Gata6 GATA binding protein 6 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:9895320 735651 Gata6 GATA binding protein 6 gene MP:0012235 abnormal liver bud morphology IAGP N RGD:5509061 20141003 MGI PMID:15767668 735651 Gata6 GATA binding protein 6 gene MP:0012278 abnormal cardiogenic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18400219 735651 Gata6 GATA binding protein 6 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:9832509 735651 Gata6 GATA binding protein 6 gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:24415953 735655 Galr1 galanin receptor 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 735655 Galr1 galanin receptor 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 735655 Galr1 galanin receptor 1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20150205 MGI PMID:23387435 735655 Galr1 galanin receptor 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 735655 Galr1 galanin receptor 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210826 MGI 735655 Galr1 galanin receptor 1 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20150205 MGI PMID:23387435 735658 Pf4 platelet factor 4 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141003 MGI PMID:14764524 735658 Pf4 platelet factor 4 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:14764524 735661 Trim50 tripartite motif-containing 50 gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22872646 735661 Trim50 tripartite motif-containing 50 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220519 MGI 735661 Trim50 tripartite motif-containing 50 gene MP:0008001 hypochlorhydria IAGP N RGD:5509061 20141003 MGI PMID:22872646 735661 Trim50 tripartite motif-containing 50 gene MP:0008006 increased stomach pH IAGP N RGD:5509061 20141003 MGI PMID:22872646 735667 Flot2 flotillin 2 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23146906 735667 Flot2 flotillin 2 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:23146906 735667 Flot2 flotillin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23146906 735667 Flot2 flotillin 2 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20151217 MGI PMID:24465508 735667 Flot2 flotillin 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20210520 MGI PMID:31138766 735667 Flot2 flotillin 2 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:23146906 735669 Bcat1 branched chain aminotransferase 1, cytosolic gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20150917 MGI PMID:24847056 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:21087515 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21087515 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:21087515 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:21087515 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:21087515 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21087515 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21087515 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:21087515 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:20547865 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0004939 abnormal B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20547865 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21087515 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:21087515 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0008234 absent spleen marginal zone IAGP N RGD:5509061 20141003 MGI PMID:21087515 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:21087515 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:21087515 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:20547865 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:20547865 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:21087515 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21087515 735675 B3gnt5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19014510 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20190221 MGI PMID:25131203 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:12368298 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:12556486 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12368298 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12556486 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17908797 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000606 decreased hepatocyte number IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17908797 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000628 abnormal mammary gland development IAGP N RGD:5509061 20141003 MGI PMID:15161927 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:15161927 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:12556486 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:12556486 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:20484573 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:20484573 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:20484573 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20231207 MGI 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20190221 MGI PMID:25131203 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20190221 MGI PMID:25131203 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12368298 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:12556486 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:12368298 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20190221 MGI PMID:25131203 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001889 delayed brain development IAGP N RGD:5509061 20141003 MGI PMID:12556486 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:23079602 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0002083 premature death IAGP N RGD:5509061 20190221 MGI PMID:25131203 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17908797 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:12368298 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:12556486 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:12556486 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12368298 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20190221 MGI PMID:25131203 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20190221 MGI PMID:25131203 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20190221 MGI PMID:25131203 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:17908797 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0003057 abnormal epicardium morphology IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:12556486 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:12368298 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:12556486 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20141003 MGI PMID:23079602 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:17908797 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20191219 MGI PMID:12368298 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20190221 MGI PMID:25131203 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0004937 dilated heart IAGP N RGD:5509061 20190221 MGI PMID:25131203 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20191219 MGI PMID:12368298 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20190221 MGI PMID:25131203 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17908797 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:12368298 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17908797 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17021013 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:15161927 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:15161927 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0006372 impaired placental function IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12556486 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:12556486 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0009397 increased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:12368298 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0009662 abnormal uterine receptivity IAGP N RGD:5509061 20141003 MGI PMID:23079602 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0009664 abnormal luminal closure IAGP N RGD:5509061 20141003 MGI PMID:23079602 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20231207 MGI 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12556486 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12368298 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20201015 MGI PMID:12368298 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0011531 abnormal syncytiotrophoblast morphology IAGP N RGD:5509061 20191219 MGI PMID:12368298 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0011629 decreased mitochondrial number IAGP N RGD:5509061 20190221 MGI PMID:25131203 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0011925 abnormal heart echocardiography feature IAGP N RGD:5509061 20190221 MGI PMID:25131203 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0011969 abnormal circulating triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:17908797 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0012099 decreased spongiotrophoblast size IAGP N RGD:5509061 20141003 MGI PMID:12556486 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0012235 abnormal liver bud morphology IAGP N RGD:5509061 20141003 MGI PMID:12446700 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0013191 increased sebaceous gland number IAGP N RGD:5509061 20141003 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0013716 hypolactation IAGP N RGD:5509061 20150611 MGI PMID:15161927 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0013782 abnormal mammary duct terminal end bud morphology IAGP N RGD:5509061 20150611 MGI PMID:15161927 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:15143190 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:12556486 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20191219 MGI PMID:12368298 735678 Ncoa6 nuclear receptor coactivator 6 gene MP:0031589 detached epicardium IAGP N RGD:5509061 20240229 MGI PMID:12446700 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16950140 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:16950140 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16950140 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16950140 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0001278 kinked vibrissae IAGP N RGD:5509061 20141003 MGI PMID:16950140 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16950140 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:11391005 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:11391004 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0001687 thin endoderm IAGP N RGD:5509061 20141003 MGI PMID:11391004 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11391005 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16950140 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11391004 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11391004 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:11391005 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0003065 abnormal liver copper level IAGP N RGD:5509061 20141003 MGI PMID:16950140 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:11391004 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0003952 abnormal copper level IAGP N RGD:5509061 20141003 MGI PMID:11391005 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0003952 abnormal copper level IAGP N RGD:5509061 20141003 MGI PMID:16950140 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0003954 abnormal Reichert's membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11391004 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11391005 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11391005 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11391004 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16950140 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:16950140 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:16950140 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20141003 MGI PMID:16950140 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0006301 abnormal mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:11391005 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0006349 decreased circulating copper level IAGP N RGD:5509061 20141003 MGI PMID:16950140 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:11391005 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16950140 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11391004 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11391005 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11391004 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0011215 decreased brain copper level IAGP N RGD:5509061 20141003 MGI PMID:11391004 735684 Slc31a1 solute carrier family 31, member 1 gene MP:0012096 decreased Reichert's membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:11391004 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15541312 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10364547 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:15344919 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20699120 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15344919 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:11404432 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:15344919 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11404432 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20699120 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001406 abnormal gait IEA N RGD:5509061 20200514 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:11404432 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:15344919 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:20699120 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10364547 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12628184 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20190502 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:12628184 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:17689977 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:15541312 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:18455244 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18455244 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21536866 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:17296559 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:15344919 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:20699120 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:15344919 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:17296559 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:15541312 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20210128 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:18701074 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:17296559 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20210826 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0003043 hypoalgesia IEA N RGD:5509061 20220519 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:15344919 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:23522044 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:15344919 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20160428 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0006352 decreased glycosylated hemoglobin level IEA N RGD:5509061 20160428 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18842882 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:17296559 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:12628184 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0008532 decreased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:15541312 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20220519 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210826 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20699120 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200514 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0009454 impaired contextual conditioning behavior IEA N RGD:5509061 20230601 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0009456 impaired cued conditioning behavior IEA N RGD:5509061 20230601 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0009713 enhanced conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:18701074 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11404432 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0009776 decreased behavioral withdrawal response IAGP N RGD:5509061 20141003 MGI PMID:11404432 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:10364547 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15541312 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17296559 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20230601 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0020422 decreased freezing behavior IEA N RGD:5509061 20230601 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0020955 increased mechanical nociceptive threshold IEA N RGD:5509061 20220519 MGI 735685 Gria1 glutamate receptor, ionotropic, AMPA1 (alpha 1) gene MP:0031391 increased locomotor activity IEA N RGD:5509061 20220421 MGI 735687 Grik1 glutamate receptor, ionotropic, kainate 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10516295 735687 Grik1 glutamate receptor, ionotropic, kainate 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220519 MGI 735687 Grik1 glutamate receptor, ionotropic, kainate 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10516295 735687 Grik1 glutamate receptor, ionotropic, kainate 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15509753 735687 Grik1 glutamate receptor, ionotropic, kainate 1 gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:10516295 735687 Grik1 glutamate receptor, ionotropic, kainate 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:11144357 735687 Grik1 glutamate receptor, ionotropic, kainate 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15509753 735687 Grik1 glutamate receptor, ionotropic, kainate 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:15673679 735687 Grik1 glutamate receptor, ionotropic, kainate 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210128 MGI 735687 Grik1 glutamate receptor, ionotropic, kainate 1 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:15673679 735687 Grik1 glutamate receptor, ionotropic, kainate 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20200514 MGI 735690 Scamp1 secretory carrier membrane protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10551807 735690 Scamp1 secretory carrier membrane protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10551807 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23671099 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0002678 increased follicle recruitment IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:17584759 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:17000861 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:17804861 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23671099 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0004167 abnormal cingulate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:23671099 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17000861 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:17804861 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:12384496 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17584759 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0009361 abnormal primordial ovarian follicle morphology IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0009362 abnormal primary ovarian follicle morphology IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17584759 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0012604 decreased glutathione level IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0021106 abnormal secondary ovarian follicle morphology IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0030623 decreased cysteine level IAGP N RGD:5509061 20180920 MGI PMID:12384496 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0030626 decreased circulating cysteine level IAGP N RGD:5509061 20180920 MGI PMID:12384496 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0031019 increased granulosa cell proliferation IAGP N RGD:5509061 20220519 MGI PMID:26083875 735691 Gclm glutamate-cysteine ligase, modifier subunit gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20220519 MGI PMID:26083875 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:9412507 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9412507 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:9412507 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:15338008 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:9412507 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:15338008 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0000866 cerebellum vermis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15338008 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15338008 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15338008 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9412507 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11699604 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9412507 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9412507 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:15338008 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:9412507 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:9412507 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9412507 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9412507 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0004144 hypotonia IAGP N RGD:5509061 20141003 MGI PMID:11699604 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0009719 reduced cerebellar foliation IAGP N RGD:5509061 20180301 MGI PMID:9412507 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9412507 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15338008 735695 Zic1 zinc finger protein of the cerebellum 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9412507 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0000284 double outlet right ventricle IEA N RGD:5509061 20151203 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0000531 right pulmonary isomerism IEA N RGD:5509061 20151203 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0000644 dextrocardia IEA N RGD:5509061 20151203 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0000650 mesocardia IEA N RGD:5509061 20151203 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0000745 tremors IEA N RGD:5509061 20160421 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0000757 herniated abdominal wall IEA N RGD:5509061 20151203 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0002192 hydrops fetalis IEA N RGD:5509061 20151203 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0003052 omphalocele IEA N RGD:5509061 20151203 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0004133 heterotaxia IEA N RGD:5509061 20151203 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0008772 increased heart ventricle size IEA N RGD:5509061 20151203 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20151203 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20151203 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0010476 coronary fistula IEA N RGD:5509061 20151203 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0010808 right-sided stomach IEA N RGD:5509061 20151203 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0010975 abnormal lung lobe morphology IEA N RGD:5509061 20151203 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0011666 double outlet right ventricle, ventricular defect committed to aorta IEA N RGD:5509061 20151203 MGI 735696 Nat8f5 N-acetyltransferase 8 (GCN5-related) family member 5 gene MP:0011668 double outlet right ventricle, Taussig bing type IEA N RGD:5509061 20151203 MGI 735701 Tac4 tachykinin 4 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:20660792 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18829546 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:18829546 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:22829581 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:22253424 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18829546 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:22829581 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:18829546 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:22253424 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:22829581 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:22829581 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22829581 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:22829581 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:18829546 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22253424 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22253424 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:22253424 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0011082 abnormal gastrointestinal motility IAGP N RGD:5509061 20141003 MGI PMID:22829581 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:22829581 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0011945 increased eating frequency IAGP N RGD:5509061 20141003 MGI PMID:22829581 735703 Glp2r glucagon-like peptide 2 receptor gene MP:0013487 abnormal Paneth cell physiology IAGP N RGD:5509061 20150319 MGI PMID:22253424 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20240523 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:17681821 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210520 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:16754854 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9230311 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17681821 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9230311 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:17681821 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:16754854 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:16754854 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002273 abnormal pulmonary alveolus epithelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16754854 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:9230311 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9230311 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:9230311 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:9230311 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20201231 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002723 abnormal immune serum protein physiology IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:17681821 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20210128 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0003394 increased cardiac output IEA N RGD:5509061 20220811 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:17681821 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20211021 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16754854 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:9230311 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0005005 abnormal self tolerance IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0005161 hematuria IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20200514 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20200514 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0005502 abnormal renal/urinary system physiology IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20200514 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20200514 MGI 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16754854 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16754854 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16754854 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0011370 increased mesangial cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17681821 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:11158608 735706 Man2a1 mannosidase 2, alpha 1 gene MP:0031084 decreased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:9230311 735710 Prph2 peripherin 2 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:3830736 735710 Prph2 peripherin 2 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:3830736 735710 Prph2 peripherin 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0001851 eye inflammation IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18763016 735710 Prph2 peripherin 2 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20210128 MGI PMID:31914632 735710 Prph2 peripherin 2 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20200604 MGI PMID:25001182 735710 Prph2 peripherin 2 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20210128 MGI PMID:31914632 735710 Prph2 peripherin 2 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:3830736 735710 Prph2 peripherin 2 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:11978760 735710 Prph2 peripherin 2 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:3830736 735710 Prph2 peripherin 2 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20200604 MGI PMID:25001182 735710 Prph2 peripherin 2 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20210128 MGI PMID:31914632 735710 Prph2 peripherin 2 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:3830736 735710 Prph2 peripherin 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11978760 735710 Prph2 peripherin 2 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11978760 735710 Prph2 peripherin 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18763016 735710 Prph2 peripherin 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200604 MGI PMID:25001182 735710 Prph2 peripherin 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20210128 MGI PMID:31914632 735710 Prph2 peripherin 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18763016 735710 Prph2 peripherin 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200604 MGI PMID:25001182 735710 Prph2 peripherin 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20210128 MGI PMID:31914632 735710 Prph2 peripherin 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11978760 735710 Prph2 peripherin 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:3830736 735710 Prph2 peripherin 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0005547 abnormal Muller cell morphology IAGP N RGD:5509061 20141003 MGI PMID:3417421 735710 Prph2 peripherin 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11978760 735710 Prph2 peripherin 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:6483282 735710 Prph2 peripherin 2 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0008445 increased retina cone cell number IAGP N RGD:5509061 20141003 MGI PMID:3830736 735710 Prph2 peripherin 2 gene MP:0008447 absent retina cone cells IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0008448 abnormal retina cone cell inner segment morphology IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:3417421 735710 Prph2 peripherin 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200604 MGI PMID:25001182 735710 Prph2 peripherin 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20210128 MGI PMID:31914632 735710 Prph2 peripherin 2 gene MP:0008453 decreased retina rod cell number IAGP N RGD:5509061 20141003 MGI PMID:11978760 735710 Prph2 peripherin 2 gene MP:0008454 absent retina rod cells IAGP N RGD:5509061 20141003 MGI PMID:705766 735710 Prph2 peripherin 2 gene MP:0008454 absent retina rod cells IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:11978760 735710 Prph2 peripherin 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:3417421 735710 Prph2 peripherin 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:3830736 735710 Prph2 peripherin 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:6483282 735710 Prph2 peripherin 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20210128 MGI PMID:31914632 735710 Prph2 peripherin 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0008516 disorganized retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:18763016 735710 Prph2 peripherin 2 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:11853768 735710 Prph2 peripherin 2 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:18763016 735710 Prph2 peripherin 2 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:3005510 735710 Prph2 peripherin 2 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:705766 735710 Prph2 peripherin 2 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200604 MGI PMID:25001182 735710 Prph2 peripherin 2 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20210128 MGI PMID:31914632 735710 Prph2 peripherin 2 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0008581 disorganized photoreceptor inner segment IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:11853768 735710 Prph2 peripherin 2 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:11978760 735710 Prph2 peripherin 2 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:18763016 735710 Prph2 peripherin 2 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:3417421 735710 Prph2 peripherin 2 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:11978760 735710 Prph2 peripherin 2 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:11978760 735710 Prph2 peripherin 2 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:18763016 735710 Prph2 peripherin 2 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200604 MGI PMID:25001182 735710 Prph2 peripherin 2 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20210128 MGI PMID:31914632 735710 Prph2 peripherin 2 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0009392 retina gliosis IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20141003 MGI PMID:7440795 735710 Prph2 peripherin 2 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200604 MGI PMID:25001182 735710 Prph2 peripherin 2 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20210128 MGI PMID:31914632 735710 Prph2 peripherin 2 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200604 MGI PMID:25001182 735710 Prph2 peripherin 2 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20210128 MGI PMID:31914632 735710 Prph2 peripherin 2 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20240404 MGI PMID:11978760 735710 Prph2 peripherin 2 gene MP:0012671 retina spots IAGP N RGD:5509061 20141003 MGI PMID:18763016 735710 Prph2 peripherin 2 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0020724 thick retina inner nuclear layer IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20200604 MGI PMID:25001182 735710 Prph2 peripherin 2 gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20210128 MGI PMID:31914632 735710 Prph2 peripherin 2 gene MP:0020813 abnormal photoreceptor outer segment disc membrane morphology IAGP N RGD:5509061 20240229 MGI PMID:37914688 735710 Prph2 peripherin 2 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:11978760 735710 Prph2 peripherin 2 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:18763016 735710 Prph2 peripherin 2 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:11978760 735710 Prph2 peripherin 2 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:18763016 735710 Prph2 peripherin 2 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:705766 735710 Prph2 peripherin 2 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:7440795 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0001304 cataract IEA N RGD:5509061 20201231 MGI 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20231207 MGI 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20231207 MGI 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17620617 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17620617 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20220811 MGI 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:17620617 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0002922 decreased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:17620617 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0009084 blind uterus IEA N RGD:5509061 20210520 MGI 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 735714 Grik3 glutamate receptor, ionotropic, kainate 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17682053 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:22624878 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:19270713 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:19270713 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:22624878 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:22624878 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0002454 abnormal macrophage antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:22624878 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19270713 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:21490400 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:21490400 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:19270713 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19270713 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0008099 abnormal plasma cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19270713 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20141003 MGI PMID:22624878 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:19270713 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0008217 abnormal B cell activation IAGP N RGD:5509061 20141003 MGI PMID:19270713 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:19270713 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:21490400 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21490400 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21490400 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:21490400 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12927796 735717 Slc3a2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21490400 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0001148 enlarged testis IAGP N RGD:5509061 20180614 MGI PMID:28576872 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20180614 MGI PMID:28576872 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20180614 MGI PMID:28576872 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20180614 MGI PMID:28576872 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20180614 MGI PMID:28576872 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0002059 abnormal seminal vesicle morphology IAGP N RGD:5509061 20180614 MGI PMID:28576872 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20180614 MGI PMID:28576872 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0002669 abnormal scrotum morphology IAGP N RGD:5509061 20180614 MGI PMID:28576872 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20180614 MGI PMID:28576872 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0002997 enlarged seminal vesicle IAGP N RGD:5509061 20180614 MGI PMID:28576872 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20180614 MGI PMID:28576872 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20180614 MGI PMID:28576872 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0004909 increased seminal vesicle weight IAGP N RGD:5509061 20180614 MGI PMID:28576872 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20180614 MGI PMID:28576872 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0013604 abnormal adult Leydig cell differentiation IAGP N RGD:5509061 20180614 MGI PMID:28576872 735718 Prl3c1 prolactin family 3, subfamily c, member 1 gene MP:0030603 increased sperm number IAGP N RGD:5509061 20180621 MGI PMID:28576872 735721 Kcns1 K+ voltage-gated channel, subfamily S, 1 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20190912 MGI PMID:29697531 735721 Kcns1 K+ voltage-gated channel, subfamily S, 1 gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20190912 MGI PMID:29697531 735721 Kcns1 K+ voltage-gated channel, subfamily S, 1 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20190912 MGI PMID:29697531 735721 Kcns1 K+ voltage-gated channel, subfamily S, 1 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20190912 MGI PMID:29697531 735721 Kcns1 K+ voltage-gated channel, subfamily S, 1 gene MP:0005407 hyperalgesia IAGP N RGD:5509061 20190912 MGI PMID:29697531 735724 Arhgef5 Rho guanine nucleotide exchange factor 5 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19713215 735724 Arhgef5 Rho guanine nucleotide exchange factor 5 gene MP:0004997 increased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:21029865 735724 Arhgef5 Rho guanine nucleotide exchange factor 5 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19713215 735724 Arhgef5 Rho guanine nucleotide exchange factor 5 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19713215 735724 Arhgef5 Rho guanine nucleotide exchange factor 5 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:19713215 735728 Gucy2d guanylate cyclase 2d gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17942483 735728 Gucy2d guanylate cyclase 2d gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:17724338 735728 Gucy2d guanylate cyclase 2d gene MP:0009943 abnormal olfactory bulb periglomerular cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17724338 735731 Gng8 guanine nucleotide binding protein (G protein), gamma 8 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20150129 MGI PMID:23836683 735731 Gng8 guanine nucleotide binding protein (G protein), gamma 8 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20150129 MGI PMID:23836683 735731 Gng8 guanine nucleotide binding protein (G protein), gamma 8 gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20150129 MGI PMID:23836683 735731 Gng8 guanine nucleotide binding protein (G protein), gamma 8 gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20150129 MGI PMID:23836683 735731 Gng8 guanine nucleotide binding protein (G protein), gamma 8 gene MP:0008779 abnormal maternal behavior IAGP N RGD:5509061 20150129 MGI PMID:23836683 735731 Gng8 guanine nucleotide binding protein (G protein), gamma 8 gene MP:0009945 abnormal accessory olfactory bulb morphology IAGP N RGD:5509061 20150129 MGI PMID:23836683 735731 Gng8 guanine nucleotide binding protein (G protein), gamma 8 gene MP:0011679 abnormal vomeronasal sensory neuron morphology IAGP N RGD:5509061 20150129 MGI PMID:23836683 735731 Gng8 guanine nucleotide binding protein (G protein), gamma 8 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:23836683 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0000013 abnormal adipose tissue distribution IAGP N RGD:5509061 20141003 MGI PMID:20548949 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:20421483 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:16329126 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0000445 short snout IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:16329126 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0000547 short limbs IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0000592 short tail IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20170601 MGI PMID:22514108 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0000753 paralysis IAGP N RGD:5509061 20161013 MGI PMID:20697156 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001258 decreased body length IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16329126 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001263 weight loss IAGP N RGD:5509061 20170601 MGI PMID:24512487 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:16329126 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20170601 MGI PMID:24512487 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001337 dry eyes IAGP N RGD:5509061 20141003 MGI PMID:16329126 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:16329126 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001697 abnormal embryo size IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:20548949 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:16329126 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15371594 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:15930266 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0001926 female infertility IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15371594 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15930266 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15371594 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20161013 MGI PMID:20697156 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16329126 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20161013 MGI PMID:20697156 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20161013 MGI PMID:26659571 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20170601 MGI PMID:24512487 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15930266 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:16329126 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:16329126 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002544 brachydactyly IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20421483 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002909 abnormal adrenal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:20548949 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20161013 MGI PMID:20697156 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:16329126 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:16329126 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15371594 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003502 increased activity of thyroid gland IAGP N RGD:5509061 20170601 MGI PMID:22514108 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003502 increased activity of thyroid gland IAGP N RGD:5509061 20170601 MGI PMID:24512487 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15371594 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20421483 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20161013 MGI PMID:20697156 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20161013 MGI PMID:26659571 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20421483 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003929 decreased heart rate variability IAGP N RGD:5509061 20141003 MGI PMID:15371594 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0004214 abnormal long bone diaphysis morphology IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0004816 abnormal class switch recombination IAGP N RGD:5509061 20141003 MGI PMID:19234474 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:17975024 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20170601 MGI PMID:22514108 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20170601 MGI PMID:22514108 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20170601 MGI PMID:24512487 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20170601 MGI PMID:22514108 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20170601 MGI PMID:24512487 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0006002 abnormal small intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:16329126 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0008018 increased facial tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15930266 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0008288 abnormal adrenal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20548949 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0008293 abnormal adrenal gland zona glomerulosa morphology IAGP N RGD:5509061 20141003 MGI PMID:20548949 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0008297 retention of the adrenal gland x-zone IAGP N RGD:5509061 20141003 MGI PMID:20548949 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0008299 adrenal cortical hyperplasia IAGP N RGD:5509061 20150305 MGI PMID:20548949 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20170601 MGI PMID:24512487 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20170601 MGI PMID:24512487 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0008853 decreased abdominal adipose tissue amount IAGP N RGD:5509061 20170601 MGI PMID:24512487 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20548949 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0010079 increased osteochondroma incidence IAGP N RGD:5509061 20141003 MGI PMID:20421483 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0010280 increased skeletal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20421483 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0010280 increased skeletal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20940146 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0010280 increased skeletal tumor incidence IAGP N RGD:5509061 20161013 MGI PMID:20697156 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0010310 increased Schwannoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15930266 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0010310 increased Schwannoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20421483 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15930266 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:20421483 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17975024 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20170601 MGI PMID:22514108 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20170601 MGI PMID:24512487 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0010363 increased fibrosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15371594 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0010971 abnormal periosteum morphology IAGP N RGD:5509061 20141003 MGI PMID:20421483 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20161013 MGI PMID:20697156 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20210422 MGI PMID:27589370 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15930266 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0011804 increased cell migration IAGP N RGD:5509061 20161013 MGI PMID:26659571 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0011881 distended duodenum IAGP N RGD:5509061 20150702 MGI PMID:16329126 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0012081 absent heart tube IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0012183 decreased paraxial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0012272 decreased axial mesoderm size IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0012498 abnormal cardiogenic plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12004056 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0013579 increased adrenal gland apoptosis IAGP N RGD:5509061 20150305 MGI PMID:20548949 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0014285 disorganized adrenal gland zona fasciculata IAGP N RGD:5509061 20230907 MGI PMID:20548949 735733 Prkar1a protein kinase, cAMP dependent regulatory, type I, alpha gene MP:0014287 decreased adrenal gland zona fasciculata size IAGP N RGD:5509061 20230907 MGI PMID:20548949 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000088 short mandible IAGP N RGD:5509061 20170323 MGI PMID:26826126 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000313 abnormal cell death IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20170323 MGI PMID:26826126 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20170323 MGI PMID:26826126 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20170323 MGI PMID:26826126 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20147379 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:20147379 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001017 abnormal stellate ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20147379 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001052 abnormal innervation pattern to muscle IAGP N RGD:5509061 20141003 MGI PMID:20147379 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001268 barrel chest IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:20147379 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0002825 abnormal notochord morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0003049 abnormal lumbar vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0003732 abnormal retina outer plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:20147379 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0004323 sternum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0004573 absent limb buds IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0005109 abnormal talus morphology IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20170323 MGI PMID:26826126 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0005252 abnormal Meibomian gland morphology IAGP N RGD:5509061 20141003 MGI PMID:20147379 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0005574 decreased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0006073 abnormal retina bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0006221 optic nerve hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0008068 absent retina ganglion cell IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0008106 decreased amacrine cell number IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0008265 abnormal hippocampus CA2 region morphology IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0008510 absent retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0008514 absent retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0009284 abnormal sympathetic neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:20147379 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20170323 MGI PMID:26826126 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0009728 abnormal calcaneum morphology IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0009768 impaired somite development IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20170323 MGI PMID:26826126 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0010395 abnormal pharyngeal arch development IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0010500 myocardium hypoplasia IAGP N RGD:5509061 20240125 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0010785 abnormal stomach pyloric region morphology IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0011261 abnormal limb mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0011262 abnormal pharyngeal arch mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0014558 decreased cortical ventricular zone thickness IAGP N RGD:5509061 20241031 MGI PMID:23483698 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0021166 delayed palatal shelf elevation IAGP N RGD:5509061 20221027 MGI PMID:26826126 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0021208 median cleft palate IAGP N RGD:5509061 20221201 MGI PMID:15254231 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:26826126 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:23649630 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0030026 small Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:26826126 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:20596238 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:26826126 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20221201 MGI PMID:26826126 735735 Sox11 SRY (sex determining region Y)-box 11 gene MP:0031583 semilunar valve hypoplasia IAGP N RGD:5509061 20240125 MGI PMID:20596238 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000094 absent alveolar process IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000125 absent incisors IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20211021 MGI 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:19154719 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20200514 MGI 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000448 pointed snout IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000629 absent mammary gland IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:10631168 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000809 absent hippocampus IAGP N RGD:5509061 20141003 MGI PMID:10631168 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000814 absent dentate gyrus IAGP N RGD:5509061 20141003 MGI PMID:10631168 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000862 absent barrels in primary somatosensory cortex IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000908 absent mesencephalic trigeminal nucleus IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:10090727 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:16163358 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0001677 absent apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:10090727 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:10090727 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:10090727 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10090727 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10090727 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10090727 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:10631168 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19154719 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0003931 absent molars IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0004790 absent upper incisors IAGP N RGD:5509061 20170928 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0004791 absent lower incisors IAGP N RGD:5509061 20170928 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:10090727 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0006302 abnormal ectomesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:10090727 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0008051 abnormal memory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22875805 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22875805 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0008262 abnormal hippocampus region morphology IAGP N RGD:5509061 20141003 MGI PMID:10631168 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:22875805 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0009097 absent endometrial glands IAGP N RGD:5509061 20150730 MGI PMID:22792274 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20210128 MGI 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10090727 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0013166 small forelimb buds IAGP N RGD:5509061 20141003 MGI PMID:10090727 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0013400 abnormal endometrial gland development IAGP N RGD:5509061 20150730 MGI PMID:22792274 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0013785 abnormal mammary gland bud morphology IAGP N RGD:5509061 20150611 MGI PMID:7958926 735737 Lef1 lymphoid enhancer binding factor 1 gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:7958926 735739 Nat1 N-acetyl transferase 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:18373979 735739 Nat1 N-acetyl transferase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:18373979 735742 Ccnb1 cyclin B1 gene MP:0000745 tremors IEA N RGD:5509061 20181227 MGI 735742 Ccnb1 cyclin B1 gene MP:0009552 urinary bladder obstruction IEA N RGD:5509061 20160811 MGI 735742 Ccnb1 cyclin B1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9539739 735742 Ccnb1 cyclin B1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735742 Ccnb1 cyclin B1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 735748 Snca synuclein, alpha gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:20106867 735748 Snca synuclein, alpha gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16269331 735748 Snca synuclein, alpha gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20181227 MGI 735748 Snca synuclein, alpha gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20106867 735748 Snca synuclein, alpha gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18622040 735748 Snca synuclein, alpha gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20106867 735748 Snca synuclein, alpha gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:24082145 735748 Snca synuclein, alpha gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:24082145 735748 Snca synuclein, alpha gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:15510220 735748 Snca synuclein, alpha gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17610578 735748 Snca synuclein, alpha gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:20106867 735748 Snca synuclein, alpha gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:24082145 735748 Snca synuclein, alpha gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16269331 735748 Snca synuclein, alpha gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20150219 MGI 735748 Snca synuclein, alpha gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0002183 gliosis IAGP N RGD:5509061 20150716 MGI PMID:25855184 735748 Snca synuclein, alpha gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:16269331 735748 Snca synuclein, alpha gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18650345 735748 Snca synuclein, alpha gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18650345 735748 Snca synuclein, alpha gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20210128 MGI 735748 Snca synuclein, alpha gene MP:0002717 abnormal male preputial gland morphology IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0002822 catalepsy IAGP N RGD:5509061 20141003 MGI PMID:18622040 735748 Snca synuclein, alpha gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:24082145 735748 Snca synuclein, alpha gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10707987 735748 Snca synuclein, alpha gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12732244 735748 Snca synuclein, alpha gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:24082145 735748 Snca synuclein, alpha gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:18650345 735748 Snca synuclein, alpha gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:24082145 735748 Snca synuclein, alpha gene MP:0003267 constipation IAGP N RGD:5509061 20141003 MGI PMID:24082145 735748 Snca synuclein, alpha gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:10707987 735748 Snca synuclein, alpha gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:18622040 735748 Snca synuclein, alpha gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:18650345 735748 Snca synuclein, alpha gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:24121116 735748 Snca synuclein, alpha gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15510220 735748 Snca synuclein, alpha gene MP:0003896 prolonged PR interval IEA N RGD:5509061 20211021 MGI 735748 Snca synuclein, alpha gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:15465911 735748 Snca synuclein, alpha gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:17227870 735748 Snca synuclein, alpha gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15510220 735748 Snca synuclein, alpha gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17610578 735748 Snca synuclein, alpha gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:24082145 735748 Snca synuclein, alpha gene MP:0004952 increased spleen weight IEA N RGD:5509061 20230601 MGI 735748 Snca synuclein, alpha gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:18650345 735748 Snca synuclein, alpha gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20150716 MGI PMID:25855184 735748 Snca synuclein, alpha gene MP:0005112 abnormal spinal cord ventral horn morphology IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 735748 Snca synuclein, alpha gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:10707987 735748 Snca synuclein, alpha gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:15465911 735748 Snca synuclein, alpha gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:18622040 735748 Snca synuclein, alpha gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:24121116 735748 Snca synuclein, alpha gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:20106867 735748 Snca synuclein, alpha gene MP:0006003 abnormal large intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:20106867 735748 Snca synuclein, alpha gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:15585343 735748 Snca synuclein, alpha gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20141003 MGI PMID:20106867 735748 Snca synuclein, alpha gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 735748 Snca synuclein, alpha gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12376616 735748 Snca synuclein, alpha gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18622040 735748 Snca synuclein, alpha gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20141003 MGI PMID:24082145 735748 Snca synuclein, alpha gene MP:0010540 long stride length IAGP N RGD:5509061 20141003 MGI PMID:18622040 735748 Snca synuclein, alpha gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:12376616 735748 Snca synuclein, alpha gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:15147505 735748 Snca synuclein, alpha gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:12376616 735748 Snca synuclein, alpha gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:15147505 735748 Snca synuclein, alpha gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 735748 Snca synuclein, alpha gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:24121116 735750 Drd3 dopamine receptor D3 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 735750 Drd3 dopamine receptor D3 gene MP:0000676 abnormal body water content IAGP N RGD:5509061 20141003 MGI PMID:15084447 735750 Drd3 dopamine receptor D3 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 735750 Drd3 dopamine receptor D3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10391470 735750 Drd3 dopamine receptor D3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16525059 735750 Drd3 dopamine receptor D3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10884517 735750 Drd3 dopamine receptor D3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10884517 735750 Drd3 dopamine receptor D3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:9402626 735750 Drd3 dopamine receptor D3 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:10391470 735750 Drd3 dopamine receptor D3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:11864730 735750 Drd3 dopamine receptor D3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:8700864 735750 Drd3 dopamine receptor D3 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:9354330 735750 Drd3 dopamine receptor D3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10884517 735750 Drd3 dopamine receptor D3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10943692 735750 Drd3 dopamine receptor D3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11864730 735750 Drd3 dopamine receptor D3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10884517 735750 Drd3 dopamine receptor D3 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:12044470 735750 Drd3 dopamine receptor D3 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:10943692 735750 Drd3 dopamine receptor D3 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:8700864 735750 Drd3 dopamine receptor D3 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:9354330 735750 Drd3 dopamine receptor D3 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:8700864 735750 Drd3 dopamine receptor D3 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:9354330 735750 Drd3 dopamine receptor D3 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10884517 735750 Drd3 dopamine receptor D3 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18644244 735750 Drd3 dopamine receptor D3 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:10391470 735750 Drd3 dopamine receptor D3 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:10884517 735750 Drd3 dopamine receptor D3 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:10884517 735750 Drd3 dopamine receptor D3 gene MP:0001666 abnormal intestinal absorption IAGP N RGD:5509061 20141003 MGI PMID:16525059 735750 Drd3 dopamine receptor D3 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:10391470 735750 Drd3 dopamine receptor D3 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:15601940 735750 Drd3 dopamine receptor D3 gene MP:0002188 small heart IEA N RGD:5509061 20210826 MGI 735750 Drd3 dopamine receptor D3 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:11864730 735750 Drd3 dopamine receptor D3 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:10884517 735750 Drd3 dopamine receptor D3 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:10884517 735750 Drd3 dopamine receptor D3 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:11864730 735750 Drd3 dopamine receptor D3 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:8700864 735750 Drd3 dopamine receptor D3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:10884517 735750 Drd3 dopamine receptor D3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:11864730 735750 Drd3 dopamine receptor D3 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:10884517 735750 Drd3 dopamine receptor D3 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:11864730 735750 Drd3 dopamine receptor D3 gene MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:11988344 735750 Drd3 dopamine receptor D3 gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:11864730 735750 Drd3 dopamine receptor D3 gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20141003 MGI PMID:16525059 735750 Drd3 dopamine receptor D3 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:11864730 735750 Drd3 dopamine receptor D3 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:15084447 735750 Drd3 dopamine receptor D3 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:15084447 735750 Drd3 dopamine receptor D3 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:15084447 735750 Drd3 dopamine receptor D3 gene MP:0005582 increased renin activity IAGP N RGD:5509061 20141003 MGI PMID:9691085 735750 Drd3 dopamine receptor D3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:12044470 735750 Drd3 dopamine receptor D3 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15084447 735750 Drd3 dopamine receptor D3 gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:16525059 735750 Drd3 dopamine receptor D3 gene MP:0006003 abnormal large intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:16525059 735750 Drd3 dopamine receptor D3 gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9691085 735750 Drd3 dopamine receptor D3 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9691085 735750 Drd3 dopamine receptor D3 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9691085 735750 Drd3 dopamine receptor D3 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:9691085 735750 Drd3 dopamine receptor D3 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15601940 735750 Drd3 dopamine receptor D3 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9691085 735750 Drd3 dopamine receptor D3 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:15371743 735750 Drd3 dopamine receptor D3 gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:10943692 735750 Drd3 dopamine receptor D3 gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:19840852 735750 Drd3 dopamine receptor D3 gene MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:11988344 735750 Drd3 dopamine receptor D3 gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20141003 MGI PMID:15371743 735750 Drd3 dopamine receptor D3 gene MP:0009775 increased behavioral withdrawal response IAGP N RGD:5509061 20141003 MGI PMID:11988344 735750 Drd3 dopamine receptor D3 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15084447 735750 Drd3 dopamine receptor D3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10391470 735750 Drd3 dopamine receptor D3 gene MP:0011432 decreased urine flow rate IAGP N RGD:5509061 20141003 MGI PMID:9691085 735750 Drd3 dopamine receptor D3 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:16525059 735750 Drd3 dopamine receptor D3 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:16525059 735750 Drd3 dopamine receptor D3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:10884517 735752 Pard3 par-3 family cell polarity regulator gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16510507 735752 Pard3 par-3 family cell polarity regulator gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16510507 735752 Pard3 par-3 family cell polarity regulator gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:16510507 735752 Pard3 par-3 family cell polarity regulator gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:16510507 735752 Pard3 par-3 family cell polarity regulator gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20181220 MGI PMID:22975380 735752 Pard3 par-3 family cell polarity regulator gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20190124 MGI PMID:28096290 735752 Pard3 par-3 family cell polarity regulator gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 735752 Pard3 par-3 family cell polarity regulator gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16510507 735752 Pard3 par-3 family cell polarity regulator gene MP:0002607 decreased basophil cell number IEA N RGD:5509061 20210128 MGI 735752 Pard3 par-3 family cell polarity regulator gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20190124 MGI PMID:28096290 735752 Pard3 par-3 family cell polarity regulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20181220 MGI PMID:22975380 735752 Pard3 par-3 family cell polarity regulator gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20181220 MGI PMID:22975380 735752 Pard3 par-3 family cell polarity regulator gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20190124 MGI PMID:28096290 735752 Pard3 par-3 family cell polarity regulator gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16510507 735752 Pard3 par-3 family cell polarity regulator gene MP:0004055 heart atrium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16510507 735752 Pard3 par-3 family cell polarity regulator gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20190124 MGI PMID:28096290 735752 Pard3 par-3 family cell polarity regulator gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20181220 MGI PMID:22975380 735752 Pard3 par-3 family cell polarity regulator gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20190124 MGI PMID:28096290 735752 Pard3 par-3 family cell polarity regulator gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20181220 MGI PMID:22975380 735752 Pard3 par-3 family cell polarity regulator gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20220519 MGI 735752 Pard3 par-3 family cell polarity regulator gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20160421 MGI 735752 Pard3 par-3 family cell polarity regulator gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:16510507 735752 Pard3 par-3 family cell polarity regulator gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20190124 MGI PMID:28096290 735752 Pard3 par-3 family cell polarity regulator gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20181220 MGI PMID:22975380 735752 Pard3 par-3 family cell polarity regulator gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20181220 MGI PMID:22975380 735752 Pard3 par-3 family cell polarity regulator gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16510507 735752 Pard3 par-3 family cell polarity regulator gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735752 Pard3 par-3 family cell polarity regulator gene MP:0012022 increased melanocyte number IAGP N RGD:5509061 20190124 MGI PMID:28096290 735753 Runx2 runt related transcription factor 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23553905 735753 Runx2 runt related transcription factor 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20151022 MGI PMID:25605327 735753 Runx2 runt related transcription factor 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15183720 735753 Runx2 runt related transcription factor 2 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:10049712 735753 Runx2 runt related transcription factor 2 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:22155527 735753 Runx2 runt related transcription factor 2 gene MP:0000065 abnormal bone marrow cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10593408 735753 Runx2 runt related transcription factor 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17786208 735753 Runx2 runt related transcription factor 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:19028669 735753 Runx2 runt related transcription factor 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0000078 abnormal supraoccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0000084 abnormal fontanelle morphology IAGP N RGD:5509061 20141003 MGI PMID:15183720 735753 Runx2 runt related transcription factor 2 gene MP:0000084 abnormal fontanelle morphology IAGP N RGD:5509061 20141003 MGI PMID:17786208 735753 Runx2 runt related transcription factor 2 gene MP:0000084 abnormal fontanelle morphology IAGP N RGD:5509061 20141003 MGI PMID:21173110 735753 Runx2 runt related transcription factor 2 gene MP:0000084 abnormal fontanelle morphology IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0000085 large anterior fontanelle IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:14688224 735753 Runx2 runt related transcription factor 2 gene MP:0000128 growth retardation of molars IAGP N RGD:5509061 20141003 MGI PMID:10357935 735753 Runx2 runt related transcription factor 2 gene MP:0000128 growth retardation of molars IAGP N RGD:5509061 20141003 MGI PMID:14688224 735753 Runx2 runt related transcription factor 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19028669 735753 Runx2 runt related transcription factor 2 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20220519 MGI 735753 Runx2 runt related transcription factor 2 gene MP:0000138 absent vertebrae IAGP N RGD:5509061 20141003 MGI PMID:21597273 735753 Runx2 runt related transcription factor 2 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0000158 absent sternum IAGP N RGD:5509061 20141003 MGI PMID:20181744 735753 Runx2 runt related transcription factor 2 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:20181744 735753 Runx2 runt related transcription factor 2 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:10072783 735753 Runx2 runt related transcription factor 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:10213384 735753 Runx2 runt related transcription factor 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:11438701 735753 Runx2 runt related transcription factor 2 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15183720 735753 Runx2 runt related transcription factor 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:20181744 735753 Runx2 runt related transcription factor 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10072783 735753 Runx2 runt related transcription factor 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10593408 735753 Runx2 runt related transcription factor 2 gene MP:0000175 absent bone marrow cell IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10049712 735753 Runx2 runt related transcription factor 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:11438701 735753 Runx2 runt related transcription factor 2 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:10049712 735753 Runx2 runt related transcription factor 2 gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:18262513 735753 Runx2 runt related transcription factor 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0000552 abnormal radius morphology IAGP N RGD:5509061 20141003 MGI PMID:10072783 735753 Runx2 runt related transcription factor 2 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:10593408 735753 Runx2 runt related transcription factor 2 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10049712 735753 Runx2 runt related transcription factor 2 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:10049712 735753 Runx2 runt related transcription factor 2 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20141003 MGI PMID:20375239 735753 Runx2 runt related transcription factor 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10049712 735753 Runx2 runt related transcription factor 2 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:20375239 735753 Runx2 runt related transcription factor 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:18262513 735753 Runx2 runt related transcription factor 2 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18262513 735753 Runx2 runt related transcription factor 2 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0001255 decreased body height IAGP N RGD:5509061 20151022 MGI PMID:25605327 735753 Runx2 runt related transcription factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11438701 735753 Runx2 runt related transcription factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15183720 735753 Runx2 runt related transcription factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20151022 MGI PMID:25605327 735753 Runx2 runt related transcription factor 2 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:14688224 735753 Runx2 runt related transcription factor 2 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20240523 MGI 735753 Runx2 runt related transcription factor 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10049712 735753 Runx2 runt related transcription factor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15183720 735753 Runx2 runt related transcription factor 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15183720 735753 Runx2 runt related transcription factor 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15183720 735753 Runx2 runt related transcription factor 2 gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:21597273 735753 Runx2 runt related transcription factor 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:23553905 735753 Runx2 runt related transcription factor 2 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:18262513 735753 Runx2 runt related transcription factor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:15183720 735753 Runx2 runt related transcription factor 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:19028669 735753 Runx2 runt related transcription factor 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:20181744 735753 Runx2 runt related transcription factor 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21597273 735753 Runx2 runt related transcription factor 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11438701 735753 Runx2 runt related transcription factor 2 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21597273 735753 Runx2 runt related transcription factor 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10049712 735753 Runx2 runt related transcription factor 2 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:15183720 735753 Runx2 runt related transcription factor 2 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:10357935 735753 Runx2 runt related transcription factor 2 gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:14688224 735753 Runx2 runt related transcription factor 2 gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20141003 MGI PMID:10357935 735753 Runx2 runt related transcription factor 2 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:19028669 735753 Runx2 runt related transcription factor 2 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:11438701 735753 Runx2 runt related transcription factor 2 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20181744 735753 Runx2 runt related transcription factor 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10072783 735753 Runx2 runt related transcription factor 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10213384 735753 Runx2 runt related transcription factor 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:21597273 735753 Runx2 runt related transcription factor 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21173110 735753 Runx2 runt related transcription factor 2 gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21597273 735753 Runx2 runt related transcription factor 2 gene MP:0003074 absent metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:21597273 735753 Runx2 runt related transcription factor 2 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:10213384 735753 Runx2 runt related transcription factor 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15183720 735753 Runx2 runt related transcription factor 2 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10072783 735753 Runx2 runt related transcription factor 2 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23553905 735753 Runx2 runt related transcription factor 2 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:20375239 735753 Runx2 runt related transcription factor 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:10593408 735753 Runx2 runt related transcription factor 2 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16751105 735753 Runx2 runt related transcription factor 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220519 MGI 735753 Runx2 runt related transcription factor 2 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:17606870 735753 Runx2 runt related transcription factor 2 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15030764 735753 Runx2 runt related transcription factor 2 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15183720 735753 Runx2 runt related transcription factor 2 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17786208 735753 Runx2 runt related transcription factor 2 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19028669 735753 Runx2 runt related transcription factor 2 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21173110 735753 Runx2 runt related transcription factor 2 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23945236 735753 Runx2 runt related transcription factor 2 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0004338 small clavicle IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0004339 absent clavicle IAGP N RGD:5509061 20141003 MGI PMID:11438701 735753 Runx2 runt related transcription factor 2 gene MP:0004339 absent clavicle IAGP N RGD:5509061 20141003 MGI PMID:19028669 735753 Runx2 runt related transcription factor 2 gene MP:0004339 absent clavicle IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0004341 absent scapula IAGP N RGD:5509061 20141003 MGI PMID:21597273 735753 Runx2 runt related transcription factor 2 gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:15030764 735753 Runx2 runt related transcription factor 2 gene MP:0004385 interparietal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0004420 parietal bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0004440 absent occipital bone IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0004440 absent occipital bone IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0004441 small occipital bone IAGP N RGD:5509061 20141003 MGI PMID:17606870 735753 Runx2 runt related transcription factor 2 gene MP:0004462 small basisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:19028669 735753 Runx2 runt related transcription factor 2 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21597273 735753 Runx2 runt related transcription factor 2 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20220519 MGI 735753 Runx2 runt related transcription factor 2 gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:21597273 735753 Runx2 runt related transcription factor 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0004690 ischium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0004693 pubis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20375239 735753 Runx2 runt related transcription factor 2 gene MP:0004900 absent zygomatic arch IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:10049712 735753 Runx2 runt related transcription factor 2 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20141003 MGI PMID:10072783 735753 Runx2 runt related transcription factor 2 gene MP:0005135 increased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:20375239 735753 Runx2 runt related transcription factor 2 gene MP:0005270 abnormal zygomatic bone morphology IEA N RGD:5509061 20220519 MGI 735753 Runx2 runt related transcription factor 2 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:10072783 735753 Runx2 runt related transcription factor 2 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17786208 735753 Runx2 runt related transcription factor 2 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19028669 735753 Runx2 runt related transcription factor 2 gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:10357935 735753 Runx2 runt related transcription factor 2 gene MP:0005359 growth retardation of incisors IAGP N RGD:5509061 20141003 MGI PMID:10357935 735753 Runx2 runt related transcription factor 2 gene MP:0005359 growth retardation of incisors IAGP N RGD:5509061 20141003 MGI PMID:14688224 735753 Runx2 runt related transcription factor 2 gene MP:0005471 decreased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:20375239 735753 Runx2 runt related transcription factor 2 gene MP:0005473 decreased triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:20375239 735753 Runx2 runt related transcription factor 2 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:20375239 735753 Runx2 runt related transcription factor 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:20181744 735753 Runx2 runt related transcription factor 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20181744 735753 Runx2 runt related transcription factor 2 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:11438701 735753 Runx2 runt related transcription factor 2 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:15183720 735753 Runx2 runt related transcription factor 2 gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20141003 MGI PMID:10213384 735753 Runx2 runt related transcription factor 2 gene MP:0006399 abnormal long bone epiphyseal ossification zone morphology IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0006402 small molars IAGP N RGD:5509061 20141003 MGI PMID:10357935 735753 Runx2 runt related transcription factor 2 gene MP:0008156 decreased diameter of tibia IAGP N RGD:5509061 20141003 MGI PMID:10593408 735753 Runx2 runt related transcription factor 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10593408 735753 Runx2 runt related transcription factor 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11438701 735753 Runx2 runt related transcription factor 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16751105 735753 Runx2 runt related transcription factor 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19028669 735753 Runx2 runt related transcription factor 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22155527 735753 Runx2 runt related transcription factor 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:10593408 735753 Runx2 runt related transcription factor 2 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:19028669 735753 Runx2 runt related transcription factor 2 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:10593408 735753 Runx2 runt related transcription factor 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11438701 735753 Runx2 runt related transcription factor 2 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:10049712 735753 Runx2 runt related transcription factor 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20240523 MGI 735753 Runx2 runt related transcription factor 2 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10049712 735753 Runx2 runt related transcription factor 2 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:21597273 735753 Runx2 runt related transcription factor 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:21597273 735753 Runx2 runt related transcription factor 2 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:14688224 735753 Runx2 runt related transcription factor 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:14688224 735753 Runx2 runt related transcription factor 2 gene MP:0009899 hyoid bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0009912 decreased hyoid bone size IAGP N RGD:5509061 20141003 MGI PMID:21173110 735753 Runx2 runt related transcription factor 2 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220519 MGI 735753 Runx2 runt related transcription factor 2 gene MP:0010864 abnormal enamel knot morphology IAGP N RGD:5509061 20180118 MGI PMID:14688224 735753 Runx2 runt related transcription factor 2 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:16751105 735753 Runx2 runt related transcription factor 2 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:16751105 735753 Runx2 runt related transcription factor 2 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:20375239 735753 Runx2 runt related transcription factor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15007057 735753 Runx2 runt related transcription factor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20151022 MGI PMID:25605327 735753 Runx2 runt related transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21597273 735753 Runx2 runt related transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23553905 735753 Runx2 runt related transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9182763 735753 Runx2 runt related transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11438701 735753 Runx2 runt related transcription factor 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20181744 735753 Runx2 runt related transcription factor 2 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0013616 decreased volumetric bone mineral density IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:20181744 735753 Runx2 runt related transcription factor 2 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20160602 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:17606870 735753 Runx2 runt related transcription factor 2 gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:19028669 735753 Runx2 runt related transcription factor 2 gene MP:0030029 wide cranial sutures IAGP N RGD:5509061 20170810 MGI PMID:9182764 735753 Runx2 runt related transcription factor 2 gene MP:0030079 small incisors IAGP N RGD:5509061 20171005 MGI PMID:10357935 735753 Runx2 runt related transcription factor 2 gene MP:0030371 delayed sagittal suture closure IAGP N RGD:5509061 20171214 MGI PMID:25244033 735753 Runx2 runt related transcription factor 2 gene MP:0030393 delayed fontanelle closure IAGP N RGD:5509061 20171207 MGI PMID:15030764 735753 Runx2 runt related transcription factor 2 gene MP:0030393 delayed fontanelle closure IAGP N RGD:5509061 20171207 MGI PMID:17786208 735753 Runx2 runt related transcription factor 2 gene MP:0030438 increased osteoblast proliferation IAGP N RGD:5509061 20171221 MGI PMID:19028669 735753 Runx2 runt related transcription factor 2 gene MP:0030498 abnormal dental lamina morphology IAGP N RGD:5509061 20180118 MGI PMID:14688224 735753 Runx2 runt related transcription factor 2 gene MP:0030507 abnormal dental papilla morphology IAGP N RGD:5509061 20180118 MGI PMID:14688224 735753 Runx2 runt related transcription factor 2 gene MP:0030521 abnormal cervical loop morphology IAGP N RGD:5509061 20180118 MGI PMID:14688224 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14976225 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14976225 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:14976225 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:16467359 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:16467359 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:16467359 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18257070 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:18371946 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:14976225 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:16467359 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:18257070 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:16467359 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:18257070 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:18257070 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16467359 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:14976225 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:14976225 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:18257070 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:16467359 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:18257070 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18257070 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0004648 decreased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:16467359 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14976225 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:16467359 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:18257070 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0008784 craniorachischisis IAGP N RGD:5509061 20141003 MGI PMID:18257070 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0009736 abnormal prostate gland branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:18371946 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:14976225 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18257070 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16467359 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:16467359 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:18257070 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:18257070 735755 Sfrp1 secreted frizzled-related protein 1 gene MP:0012182 abnormal presomitic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18257070 735758 Aadat aminoadipate aminotransferase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15282294 735758 Aadat aminoadipate aminotransferase gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:15282294 735758 Aadat aminoadipate aminotransferase gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20141003 MGI PMID:15282294 735758 Aadat aminoadipate aminotransferase gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15282294 735758 Aadat aminoadipate aminotransferase gene MP:0003153 early eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:15282294 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20240523 MGI 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:12355066 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12355066 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0001199 thin skin IEA N RGD:5509061 20240523 MGI 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20240523 MGI 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19428613 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15689543 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16513268 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:19428613 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20240523 MGI 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9655611 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20240523 MGI 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12598897 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:19428613 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:15689543 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:19428613 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20230601 MGI PMID:26360410 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12355066 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:19428613 735761 Ptprz1 protein tyrosine phosphatase receptor type Z, polypeptide 1 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20230601 MGI PMID:26360410 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16554359 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:16554359 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:17303760 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21989910 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21989910 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21989910 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0001689 incomplete somite formation IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0001725 abnormal umbilical cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16199874 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:16554359 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:17303760 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0003410 abnormal artery development IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0003833 decreased satellite cell number IAGP N RGD:5509061 20141003 MGI PMID:21989910 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:21989910 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0006006 increased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:19631204 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:17303760 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20141003 MGI PMID:17303760 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:17303760 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:21989910 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:21989910 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0009410 abnormal skeletal muscle satellite cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21989910 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0010406 common atrium IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17303760 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0010432 common ventricle IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:17303760 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0010601 thick pulmonary valve IAGP N RGD:5509061 20141003 MGI PMID:17303760 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17303760 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21989910 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15680351 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15107403 735763 Hey1 hairy/enhancer-of-split related with YRPW motif 1 gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:21989910 735768 Gjd2 gap junction protein, delta 2 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18498740 735768 Gjd2 gap junction protein, delta 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11516403 735768 Gjd2 gap junction protein, delta 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11516404 735768 Gjd2 gap junction protein, delta 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15924862 735768 Gjd2 gap junction protein, delta 2 gene MP:0002911 abnormal inhibitory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:11516404 735768 Gjd2 gap junction protein, delta 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:11516404 735768 Gjd2 gap junction protein, delta 2 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:18258229 735768 Gjd2 gap junction protein, delta 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:12064624 735768 Gjd2 gap junction protein, delta 2 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:18498740 735768 Gjd2 gap junction protein, delta 2 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:18498740 735768 Gjd2 gap junction protein, delta 2 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17395748 735768 Gjd2 gap junction protein, delta 2 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18258229 735768 Gjd2 gap junction protein, delta 2 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17395748 735768 Gjd2 gap junction protein, delta 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:11516404 735768 Gjd2 gap junction protein, delta 2 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15791644 735768 Gjd2 gap junction protein, delta 2 gene MP:0005291 abnormal glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18258229 735768 Gjd2 gap junction protein, delta 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:11516404 735769 H2az1 H2A.Z variant histone 1 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20191003 MGI PMID:30842416 735769 H2az1 H2A.Z variant histone 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20191003 MGI PMID:30842416 735769 H2az1 H2A.Z variant histone 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20221103 MGI 735769 H2az1 H2A.Z variant histone 1 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:11516949 735769 H2az1 H2A.Z variant histone 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20230601 MGI 735769 H2az1 H2A.Z variant histone 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11516949 735769 H2az1 H2A.Z variant histone 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20221103 MGI 735769 H2az1 H2A.Z variant histone 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20221103 MGI 735771 Ykt6 YKT6 v-SNARE homolog (S. cerevisiae) gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20230601 MGI 735771 Ykt6 YKT6 v-SNARE homolog (S. cerevisiae) gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210520 MGI 735771 Ykt6 YKT6 v-SNARE homolog (S. cerevisiae) gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IEA N RGD:5509061 20240919 MGI 735771 Ykt6 YKT6 v-SNARE homolog (S. cerevisiae) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 735771 Ykt6 YKT6 v-SNARE homolog (S. cerevisiae) gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210826 MGI 735771 Ykt6 YKT6 v-SNARE homolog (S. cerevisiae) gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IEA N RGD:5509061 20240919 MGI 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:17537961 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:23922229 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:21156207 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:23922229 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:24155976 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17537961 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20100831 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160107 MGI PMID:25725421 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:17537961 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20100831 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:23922229 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20190207 MGI PMID:22914087 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20190207 MGI PMID:22914087 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:23922229 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001394 circling IAGP N RGD:5509061 20190207 MGI PMID:22914087 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001399 hyperactivity IAGP N RGD:5509061 20230309 MGI PMID:33910599 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23922229 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:17537961 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160107 MGI PMID:25725421 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20190207 MGI PMID:22914087 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20190207 MGI PMID:22914087 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:24155976 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:24155976 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230309 MGI PMID:33910599 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0001957 apnea IAGP N RGD:5509061 20180517 MGI PMID:29329111 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20230309 MGI PMID:33910599 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:17537961 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:20100831 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:22908258 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:24152123 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002064 seizures IAGP N RGD:5509061 20180517 MGI PMID:29329111 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19409490 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23922229 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17537961 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17881658 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19409490 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22908258 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23922229 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24152123 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24155976 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20160107 MGI PMID:25725421 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20180517 MGI PMID:29329111 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24152123 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:17537961 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002194 maximal tonic hindlimb extension seizures IAGP N RGD:5509061 20141003 MGI PMID:20100831 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:20100831 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20190207 MGI PMID:22914087 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:17537961 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20100831 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:17881658 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:20100831 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:21156207 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:24155976 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20230309 MGI PMID:33910599 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20190207 MGI PMID:22914087 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0002980 abnormal postural reflex IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:24155976 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20230309 MGI PMID:33910599 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0003462 abnormal response to novel odor IAGP N RGD:5509061 20190207 MGI PMID:22914087 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:17537961 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20160107 MGI PMID:25725421 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20100831 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0003996 clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:22908258 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:17537961 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:17881658 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20100831 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:21156207 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:22908258 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20160107 MGI PMID:25725421 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:20100831 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:24155976 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20160107 MGI PMID:25725421 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:23922229 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:24155976 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20180517 MGI PMID:29329111 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:17537961 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0006110 ventricular fibrillation IAGP N RGD:5509061 20141003 MGI PMID:24155976 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20160107 MGI PMID:25725421 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20230309 MGI PMID:33910599 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20190207 MGI PMID:22914087 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23922229 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:21156207 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:17881658 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:20100831 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20230309 MGI PMID:33910599 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:20100831 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:22908258 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20160107 MGI PMID:25725421 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20180517 MGI PMID:29329111 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20230309 MGI PMID:33910599 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20160107 MGI PMID:25725421 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20190207 MGI PMID:22914087 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20230309 MGI PMID:33910599 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20141003 MGI PMID:24155976 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180517 MGI PMID:29329111 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20160107 MGI PMID:25725421 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20160107 MGI PMID:25725421 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23922229 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0010504 abnormal RR interval IAGP N RGD:5509061 20141003 MGI PMID:24155976 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:24155976 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0010636 bundle branch block IAGP N RGD:5509061 20141003 MGI PMID:24155976 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16921370 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17537961 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17881658 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20100831 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21156207 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23922229 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20160107 MGI PMID:25725421 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21156207 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22908258 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20230309 MGI PMID:33910599 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20230309 MGI PMID:33910599 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0011622 abnormal habituation to a novel odor IAGP N RGD:5509061 20190207 MGI PMID:22914087 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20190207 MGI PMID:22914087 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0014253 decreased paired-pulse ratio IAGP N RGD:5509061 20230706 MGI PMID:25725421 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0014378 increased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:22914087 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20190207 MGI PMID:22914087 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0020852 abnormal olfactory behavior IAGP N RGD:5509061 20190207 MGI PMID:22914087 735778 Scn1a sodium channel, voltage-gated, type I, alpha gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22914087 735781 Adcy7 adenylate cyclase 7 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:23178822 735781 Adcy7 adenylate cyclase 7 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:17135423 735781 Adcy7 adenylate cyclase 7 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23178822 735781 Adcy7 adenylate cyclase 7 gene MP:0011085 postnatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 735781 Adcy7 adenylate cyclase 7 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17135423 735788 Apob apolipoprotein B gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8460149 735788 Apob apolipoprotein B gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 735788 Apob apolipoprotein B gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8692825 735788 Apob apolipoprotein B gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 735788 Apob apolipoprotein B gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10893242 735788 Apob apolipoprotein B gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11839763 735788 Apob apolipoprotein B gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8692825 735788 Apob apolipoprotein B gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8921909 735788 Apob apolipoprotein B gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9852051 735788 Apob apolipoprotein B gene MP:0000184 abnormal circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8921909 735788 Apob apolipoprotein B gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10893242 735788 Apob apolipoprotein B gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11839763 735788 Apob apolipoprotein B gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7878058 735788 Apob apolipoprotein B gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8460149 735788 Apob apolipoprotein B gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 735788 Apob apolipoprotein B gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10705993 735788 Apob apolipoprotein B gene MP:0000231 hypertension IAGP N RGD:5509061 20170209 MGI PMID:18160459 735788 Apob apolipoprotein B gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:7597652 735788 Apob apolipoprotein B gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:7878058 735788 Apob apolipoprotein B gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:8460149 735788 Apob apolipoprotein B gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:8921909 735788 Apob apolipoprotein B gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9502790 735788 Apob apolipoprotein B gene MP:0001260 increased body weight IAGP N RGD:5509061 20170420 MGI PMID:9202070 735788 Apob apolipoprotein B gene MP:0001261 obese IAGP N RGD:5509061 20170209 MGI PMID:18160459 735788 Apob apolipoprotein B gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170420 MGI PMID:9202070 735788 Apob apolipoprotein B gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:8692825 735788 Apob apolipoprotein B gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170209 MGI PMID:18160459 735788 Apob apolipoprotein B gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20170420 MGI PMID:9202070 735788 Apob apolipoprotein B gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20170209 MGI PMID:18160459 735788 Apob apolipoprotein B gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20170420 MGI PMID:9202070 735788 Apob apolipoprotein B gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20170209 MGI PMID:18160459 735788 Apob apolipoprotein B gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:9026532 735788 Apob apolipoprotein B gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9502790 735788 Apob apolipoprotein B gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:7597652 735788 Apob apolipoprotein B gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:8460149 735788 Apob apolipoprotein B gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:8921909 735788 Apob apolipoprotein B gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9502790 735788 Apob apolipoprotein B gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:8855280 735788 Apob apolipoprotein B gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17872464 735788 Apob apolipoprotein B gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20170209 MGI PMID:18160459 735788 Apob apolipoprotein B gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9852051 735788 Apob apolipoprotein B gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:10893242 735788 Apob apolipoprotein B gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:11839763 735788 Apob apolipoprotein B gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:10893242 735788 Apob apolipoprotein B gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11839763 735788 Apob apolipoprotein B gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:8692825 735788 Apob apolipoprotein B gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:8460149 735788 Apob apolipoprotein B gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8855280 735788 Apob apolipoprotein B gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8855280 735788 Apob apolipoprotein B gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0003394 increased cardiac output IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20170420 MGI PMID:9202070 735788 Apob apolipoprotein B gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 735788 Apob apolipoprotein B gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20170420 MGI PMID:9202070 735788 Apob apolipoprotein B gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10893242 735788 Apob apolipoprotein B gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11839763 735788 Apob apolipoprotein B gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8921909 735788 Apob apolipoprotein B gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9852051 735788 Apob apolipoprotein B gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20170209 MGI PMID:18160459 735788 Apob apolipoprotein B gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20170420 MGI PMID:9202070 735788 Apob apolipoprotein B gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:10705993 735788 Apob apolipoprotein B gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11839763 735788 Apob apolipoprotein B gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:7878058 735788 Apob apolipoprotein B gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:8921909 735788 Apob apolipoprotein B gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9502790 735788 Apob apolipoprotein B gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20170420 MGI PMID:9202070 735788 Apob apolipoprotein B gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18385042 735788 Apob apolipoprotein B gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7878058 735788 Apob apolipoprotein B gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20170420 MGI PMID:9202070 735788 Apob apolipoprotein B gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17872464 735788 Apob apolipoprotein B gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20170209 MGI PMID:18160459 735788 Apob apolipoprotein B gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:17872464 735788 Apob apolipoprotein B gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20170209 MGI PMID:18160459 735788 Apob apolipoprotein B gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20170420 MGI PMID:9202070 735788 Apob apolipoprotein B gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20170420 MGI PMID:9202070 735788 Apob apolipoprotein B gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18385042 735788 Apob apolipoprotein B gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17872464 735788 Apob apolipoprotein B gene MP:0006116 calcified aortic valve IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0010139 aortitis IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0010332 abnormal circulating apolipoprotein level IAGP N RGD:5509061 20220120 MGI PMID:10705993 735788 Apob apolipoprotein B gene MP:0010332 abnormal circulating apolipoprotein level IAGP N RGD:5509061 20220120 MGI PMID:8921909 735788 Apob apolipoprotein B gene MP:0010912 herniated liver IAGP N RGD:5509061 20141003 MGI PMID:9502790 735788 Apob apolipoprotein B gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7593600 735788 Apob apolipoprotein B gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9502790 735788 Apob apolipoprotein B gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10893242 735788 Apob apolipoprotein B gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11839763 735788 Apob apolipoprotein B gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7878058 735788 Apob apolipoprotein B gene MP:0011572 abnormal aorta bulb morphology IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0012688 abnormal heart ventricles weight IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0013277 abnormal fasting circulating glucose level IAGP N RGD:5509061 20160609 MGI PMID:25231636 735788 Apob apolipoprotein B gene MP:0020515 abnormal visceral yolk sac endoderm morphology IAGP N RGD:5509061 20180125 MGI PMID:9026532 735788 Apob apolipoprotein B gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:8855280 735788 Apob apolipoprotein B gene MP:0031566 small aortic valve IAGP N RGD:5509061 20240125 MGI PMID:25231636 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20180719 MGI PMID:14605248 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20180719 MGI PMID:9114002 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20180719 MGI PMID:14605248 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20180719 MGI PMID:14605248 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20180719 MGI PMID:9114002 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180719 MGI PMID:12835402 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20180719 MGI PMID:14605248 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20180719 MGI PMID:9114002 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20180719 MGI PMID:9114002 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20180719 MGI PMID:9114002 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20180719 MGI PMID:9114002 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20180719 MGI PMID:14605248 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20180719 MGI PMID:9114002 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20180719 MGI PMID:9114002 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20180719 MGI PMID:14605248 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20180719 MGI PMID:12124211 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20180719 MGI PMID:9114002 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20180719 MGI PMID:9114002 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:9114002 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:9114002 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20180719 MGI PMID:14605248 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0020409 abnormal cardiac thrombosis IAGP N RGD:5509061 20180719 MGI PMID:9114002 735790 Actc1 actin, alpha, cardiac muscle 1 gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:9114002 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:11296258 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:19004821 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:11350923 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201231 MGI 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:12890773 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:16939638 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16939638 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:11350923 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12890773 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:15870896 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0001752 abnormal hypothalamus secretion IAGP N RGD:5509061 20141003 MGI PMID:19004821 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11496122 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11520183 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:20852623 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:16939638 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:11520183 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19004821 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0002570 alcohol aversion IAGP N RGD:5509061 20141003 MGI PMID:15525770 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11296258 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15870896 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:15870896 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15870896 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0002802 abnormal discrimination learning IAGP N RGD:5509061 20141003 MGI PMID:16939638 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:15525770 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:12962913 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:16939638 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19004821 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0002969 impaired social transmission of food preference IAGP N RGD:5509061 20141003 MGI PMID:16939638 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0003194 abnormal frequency of paradoxical sleep IAGP N RGD:5509061 20141003 MGI PMID:12890773 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:19004821 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:20852623 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0003470 abnormal summary potential IAGP N RGD:5509061 20141003 MGI PMID:19004821 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:11496122 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:11520183 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:15525770 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:19004821 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:11296258 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0004184 abnormal baroreceptor physiology IAGP N RGD:5509061 20141003 MGI PMID:11296258 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16939638 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0004924 abnormal behavior IEA N RGD:5509061 20201231 MGI 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15870896 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11350923 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11520183 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:15870896 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15870896 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:16939638 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11350923 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11496122 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11520183 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19004821 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0009436 fragmentation of sleep/wake states IAGP N RGD:5509061 20141003 MGI PMID:12890773 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:15525770 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0009745 abnormal behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12962913 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0009751 enhanced behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:15525770 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:15525770 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160421 MGI 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20852623 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11350923 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 735793 Cacna1b calcium channel, voltage-dependent, N type, alpha 1B subunit gene MP:0021198 abnormal sleep duration IAGP N RGD:5509061 20220922 MGI PMID:12890773 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0000745 tremors IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0000778 abnormal nervous system tract morphology IAGP N RGD:5509061 20220331 MGI PMID:35171680 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20220331 MGI PMID:35171680 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20220331 MGI PMID:35171680 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0000921 demyelination IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0001263 weight loss IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0001393 ataxia IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0001393 ataxia IAGP N RGD:5509061 20220331 MGI PMID:35171680 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0001405 impaired coordination IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0001405 impaired coordination IAGP N RGD:5509061 20220331 MGI PMID:35171680 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0001523 impaired righting response IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20220331 MGI PMID:35171680 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0002083 premature death IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0002083 premature death IAGP N RGD:5509061 20220331 MGI PMID:35171680 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20220331 MGI PMID:35171680 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20220331 MGI PMID:35171680 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20220331 MGI PMID:35171680 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0005323 dystonia IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0005405 axon degeneration IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0006099 thin cerebellar granule layer IAGP N RGD:5509061 20220331 MGI PMID:35171680 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20220331 MGI PMID:35171680 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20240229 MGI PMID:38031972 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0013438 dysmyelination IAGP N RGD:5509061 20200806 MGI PMID:32463361 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0013438 dysmyelination IAGP N RGD:5509061 20220331 MGI PMID:35171680 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20220331 MGI PMID:35171680 735794 Tubb4a tubulin, beta 4A class IVA gene MP:0031496 motor developmental delay IAGP N RGD:5509061 20230810 MGI PMID:32463361 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0000054 delayed ear emergence IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0000274 enlarged heart IEA N RGD:5509061 20200402 MGI 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:11344259 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:12876201 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15541879 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20160915 MGI PMID:20603624 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15541879 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160915 MGI PMID:20603624 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:12876201 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:15963492 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:15450117 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:10235262 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20160915 MGI PMID:20603624 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0002083 premature death IAGP N RGD:5509061 20160915 MGI PMID:20603624 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:11344259 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:7870173 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15456819 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0002313 abnormal tidal volume IAGP N RGD:5509061 20141003 MGI PMID:15450117 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0002338 abnormal pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:15450117 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15963492 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15963492 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:15963492 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20200402 MGI 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:12876201 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0003280 urinary incontinence IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20141003 MGI PMID:15541879 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20160915 MGI PMID:20603624 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:15541879 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:7870173 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0004165 abnormal lateral geniculate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:11344259 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0004165 abnormal lateral geniculate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18757739 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:12876201 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20160915 MGI PMID:20603624 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:15963492 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16253349 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15963492 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:15450117 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20150910 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18757739 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0005575 increased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:15450117 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0005585 increased tidal volume IAGP N RGD:5509061 20141003 MGI PMID:15450117 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20141003 MGI PMID:11344259 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0006276 abnormal autonomic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0009436 fragmentation of sleep/wake states IAGP N RGD:5509061 20160915 MGI PMID:20603624 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0009475 abnormal nicotine-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:10235262 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0009475 abnormal nicotine-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:7870173 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0009646 urinary bladder inflammation IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20150402 MGI PMID:18083057 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:10771006 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20141003 MGI PMID:18083057 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0011620 abnormal habituation to a new environment IAGP N RGD:5509061 20160915 MGI PMID:20603624 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0011625 cystolithiasis IAGP N RGD:5509061 20141003 MGI PMID:10531434 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12876201 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0012349 increased susceptibility to induction of seizure by inducing agent IAGP N RGD:5509061 20160915 MGI PMID:20603624 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0020160 abnormal behavioral response to nicotine IAGP N RGD:5509061 20160915 MGI PMID:20603624 735795 Chrnb2 cholinergic receptor nicotinic beta 2 subunit gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:20603624 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20230119 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20230119 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20180712 MGI PMID:22834956 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20180712 MGI PMID:22834956 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17219415 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17219415 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20230119 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15010296 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15955095 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:16195376 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20080498 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:15010296 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:15280217 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:15665986 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:15955095 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16195376 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16455232 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:9799606 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:6863894 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000425 loss of eyelid cilia IAGP N RGD:5509061 20150212 MGI PMID:2458328 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000425 loss of eyelid cilia IAGP N RGD:5509061 20160505 MGI PMID:24845637 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:9799606 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:10536052 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:10536052 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000580 deformed nails IAGP N RGD:5509061 20141003 MGI PMID:16455232 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000583 long toenails IAGP N RGD:5509061 20141003 MGI PMID:15665986 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000583 long toenails IAGP N RGD:5509061 20141003 MGI PMID:15955095 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000583 long toenails IAGP N RGD:5509061 20141003 MGI PMID:20080498 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000583 long toenails IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16682947 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20111116 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000629 absent mammary gland IEA N RGD:5509061 20111116 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20141003 MGI PMID:2458328 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000647 abnormal sebaceous gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9832318 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000649 sebaceous gland atrophy IEA N RGD:5509061 20111116 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20180712 MGI PMID:22834956 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:15665986 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:6863894 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:8281013 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:15955095 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:6863894 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:6863894 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:15665986 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:15955095 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:8281013 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001200 thick skin IAGP N RGD:5509061 20240418 MGI PMID:22964757 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001201 translucent skin IEA N RGD:5509061 20111116 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001203 increased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:16682947 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001204 decreased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:15498793 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001210 skin ridges IEA N RGD:5509061 20170914 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:15280217 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:15665986 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:15955095 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:20080498 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:6863894 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:8281013 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20240418 MGI PMID:22964757 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:8281013 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001214 skin hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15280217 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16455232 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001219 thick epidermis IAGP N RGD:5509061 20190530 MGI PMID:21020475 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20190530 MGI PMID:21020475 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001239 abnormal epidermis stratum granulosum morphology IAGP N RGD:5509061 20141003 MGI PMID:20080498 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:16455232 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:15665986 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:15955095 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20190530 MGI PMID:21020475 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15665986 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15955095 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:15665986 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:14946445 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:15010296 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:15280217 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:15665986 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:15955095 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:16455232 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:20080498 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:9799606 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:9832316 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001247 dermal cyst IAGP N RGD:5509061 20141003 MGI PMID:9832318 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001260 increased body weight IAGP N RGD:5509061 20240418 MGI PMID:22964757 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001262 decreased body weight IEA N RGD:5509061 20111116 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001265 decreased body size IEA N RGD:5509061 20141003 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:6863894 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001279 wavy vibrissae IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001280 loss of vibrissae IAGP N RGD:5509061 20141003 MGI PMID:16455232 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001282 short vibrissae IAGP N RGD:5509061 20141003 MGI PMID:6863894 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001284 absent vibrissae IEA N RGD:5509061 20230119 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20160505 MGI PMID:24845637 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20150212 MGI PMID:2458328 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20160505 MGI PMID:24845637 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001345 Meibomian gland atrophy IAGP N RGD:5509061 20141003 MGI PMID:2458328 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:15955095 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:20080498 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:6863894 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180712 MGI PMID:22834956 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20240418 MGI PMID:22964757 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001785 edema IAGP N RGD:5509061 20160505 MGI PMID:24845637 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001824 abnormal thymus involution IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:2458328 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001851 eye inflammation IAGP N RGD:5509061 20160505 MGI PMID:24845637 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:16455232 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:6863894 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9832316 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:186616 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:201855 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:4310515 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:12531021 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:15280217 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:15665986 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:15955095 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:16195376 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:9832316 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:6863894 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12531021 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15955095 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17219415 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20180712 MGI PMID:22834956 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:6863894 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20180712 MGI PMID:22834956 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002346 abnormal lymph node secondary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:16455232 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:15955095 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20180712 MGI PMID:22834956 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20230119 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20141003 MGI PMID:9832316 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:15665986 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:8281013 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20160317 MGI PMID:9832316 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:14471512 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:8281013 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20190530 MGI PMID:21020475 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:16977324 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003637 cochlear ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10536052 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:10536052 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:15955095 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20160505 MGI PMID:24845637 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:16977324 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003813 abnormal hair follicle dermal papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:6863894 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:9832316 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003815 hairless IAGP N RGD:5509061 20141003 MGI PMID:9832318 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003815 hairless IAGP N RGD:5509061 20180712 MGI PMID:22834956 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003865 lymph node inflammation IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:12531021 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20180712 MGI PMID:22834956 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0004126 thin hypodermis IAGP N RGD:5509061 20141003 MGI PMID:15665986 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15498793 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10536052 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10536052 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:12531021 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:16682947 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:17219415 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0004504 decreased incidence of tumors by UV induction IAGP N RGD:5509061 20141003 MGI PMID:15498793 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0004504 decreased incidence of tumors by UV induction IAGP N RGD:5509061 20141003 MGI PMID:16977324 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0004504 decreased incidence of tumors by UV induction IAGP N RGD:5509061 20141003 MGI PMID:17219415 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0004526 absent cochlear hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:10536052 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:16235133 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:20080498 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20230119 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:310859 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0005081 abnormal dermis reticular layer morphology IEA N RGD:5509061 20111116 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:6447727 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20230119 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0005251 blepharitis IAGP N RGD:5509061 20160505 MGI PMID:24845637 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0005252 abnormal Meibomian gland morphology IAGP N RGD:5509061 20141003 MGI PMID:2458328 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:15955095 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:16455232 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:11013214 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:16977324 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0005515 uveitis IAGP N RGD:5509061 20160505 MGI PMID:24845637 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0006162 thick eyelids IAGP N RGD:5509061 20150212 MGI PMID:2458328 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20180712 MGI PMID:22834956 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0008507 thin retina ganglion layer IAGP N RGD:5509061 20141003 MGI PMID:10536052 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0008513 thin retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:10536052 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20230119 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009003 abnormal vibrissa number IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009003 abnormal vibrissa number IAGP N RGD:5509061 20141003 MGI PMID:20080498 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20141003 MGI PMID:20080498 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20141003 MGI PMID:8281013 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20240418 MGI PMID:22964757 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009600 hypergranulosis IAGP N RGD:5509061 20141003 MGI PMID:20080498 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009601 epidermis stratum granulosum hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20080498 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009623 enlarged inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009635 enlarged popliteal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:16682947 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009704 increased skin squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12531021 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009722 abnormal nipple development IEA N RGD:5509061 20150219 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:17219415 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009815 decreased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:17219415 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20170309 MGI PMID:9799606 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0009935 abnormal Meibomian gland acinus morphology IAGP N RGD:5509061 20150212 MGI PMID:2458328 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0010234 abnormal vibrissa follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12531021 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0010680 abnormal skin adnexa physiology IEA N RGD:5509061 20141003 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0010682 abnormal hair follicle infundibulum morphology IAGP N RGD:5509061 20141003 MGI PMID:20080498 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0010683 dilated hair follicle infundibulum IAGP N RGD:5509061 20141003 MGI PMID:20080498 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0010683 dilated hair follicle infundibulum IAGP N RGD:5509061 20141003 MGI PMID:9799606 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0010683 dilated hair follicle infundibulum IAGP N RGD:5509061 20180524 MGI PMID:15010296 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0010684 abnormal hair follicle outer root sheath morphology IAGP N RGD:5509061 20180524 MGI PMID:15010296 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:19513791 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20180524 MGI PMID:15010296 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0010687 absent hair follicle dermal papilla IAGP N RGD:5509061 20141003 MGI PMID:9799606 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0010699 dilated hair follicle IAGP N RGD:5509061 20160317 MGI PMID:15665986 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0010699 dilated hair follicle IAGP N RGD:5509061 20240620 MGI PMID:8103276 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16682947 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20180712 MGI PMID:22834956 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20141003 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0011225 lymph node medullary cord hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0012022 increased melanocyte number IAGP N RGD:5509061 20180712 MGI PMID:22834956 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12531021 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0012725 small sebaceous gland IAGP N RGD:5509061 20141218 MGI PMID:9832318 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0012728 abnormal somite border morphology IAGP N RGD:5509061 20180712 MGI PMID:22834956 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0013379 decreased sebocyte cell number IAGP N RGD:5509061 20141218 MGI PMID:9832318 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0013390 Meibomian gland cyst IAGP N RGD:5509061 20150212 MGI PMID:2458328 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0013392 Meibomian gland inflammation IAGP N RGD:5509061 20160505 MGI PMID:24845637 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0013529 decreased nipple number IEA N RGD:5509061 20150219 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0013585 thymus cortex atrophy IAGP N RGD:5509061 20150319 MGI PMID:7640630 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0013745 abnormal eyelid margin morphology IAGP N RGD:5509061 20150416 MGI PMID:2458328 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0014082 decreased small intestinal villus height IAGP N RGD:5509061 20160310 MGI PMID:10536052 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0030031 abnormal forehead morphology IEA N RGD:5509061 20170914 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0030570 abnormal piliary canal morphology IEA N RGD:5509061 20180524 MGI 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0030571 dilated piliary canal IAGP N RGD:5509061 20180524 MGI PMID:15010296 735796 Hr lysine demethylase and nuclear receptor corepressor gene MP:0030571 dilated piliary canal IAGP N RGD:5509061 20180524 MGI PMID:15280217 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0001422 abnormal drinking behavior IAGP N RGD:5509061 20141003 MGI PMID:14581612 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:17786199 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:14581612 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:16597741 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:23929777 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:12692122 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:17008604 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:14581612 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:23929777 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:16597741 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0003280 urinary incontinence IAGP N RGD:5509061 20141003 MGI PMID:17948126 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23929777 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17786199 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0004597 increased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20141003 MGI PMID:15925108 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:16597741 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20181129 MGI PMID:30143574 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:17008604 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0005203 abnormal trabecular meshwork morphology IAGP N RGD:5509061 20150416 MGI PMID:25143588 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0005258 ocular hypertension IAGP N RGD:5509061 20150416 MGI PMID:25143588 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0005316 abnormal response to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:12692122 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:23929777 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0005611 decreased circulating antidiuretic hormone level IAGP N RGD:5509061 20141003 MGI PMID:14581612 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:15925108 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:12692122 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0008997 increased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:14581612 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0008998 decreased blood osmolality IAGP N RGD:5509061 20141003 MGI PMID:14581612 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:17948126 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0011942 decreased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:14581612 735797 Trpv4 transient receptor potential cation channel, subfamily V, member 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15925108 735802 Actb actin, beta gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17877786 735802 Actb actin, beta gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17877786 735802 Actb actin, beta gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23544080 735802 Actb actin, beta gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23544080 735802 Actb actin, beta gene MP:0000767 abnormal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:14661057 735802 Actb actin, beta gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:14661057 735802 Actb actin, beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16028230 735802 Actb actin, beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17877786 735802 Actb actin, beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17987666 735802 Actb actin, beta gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:17877786 735802 Actb actin, beta gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14661057 735802 Actb actin, beta gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14661057 735802 Actb actin, beta gene MP:0002035 increased leiomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14661057 735802 Actb actin, beta gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15254588 735802 Actb actin, beta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14661057 735802 Actb actin, beta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15254588 735802 Actb actin, beta gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23544080 735802 Actb actin, beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21240280 735802 Actb actin, beta gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:23544080 735802 Actb actin, beta gene MP:0002534 abnormal type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23544080 735802 Actb actin, beta gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:15254588 735802 Actb actin, beta gene MP:0002683 delayed fertility IAGP N RGD:5509061 20141003 MGI PMID:17877786 735802 Actb actin, beta gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17877786 735802 Actb actin, beta gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17877786 735802 Actb actin, beta gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:14661057 735802 Actb actin, beta gene MP:0002997 enlarged seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:14661057 735802 Actb actin, beta gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9608737 735802 Actb actin, beta gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:20976199 735802 Actb actin, beta gene MP:0004524 short cochlear hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:20976199 735802 Actb actin, beta gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20181122 MGI PMID:30012594 735802 Actb actin, beta gene MP:0004529 decreased outer hair cell stereocilia number IAGP N RGD:5509061 20181122 MGI PMID:30012594 735802 Actb actin, beta gene MP:0004531 short outer hair cell stereocilia IAGP N RGD:5509061 20181122 MGI PMID:30012594 735802 Actb actin, beta gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20141003 MGI PMID:20976199 735802 Actb actin, beta gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20181122 MGI PMID:30012594 735802 Actb actin, beta gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:23544080 735802 Actb actin, beta gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20150101 MGI PMID:23185019 735802 Actb actin, beta gene MP:0004972 abnormal regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23544080 735802 Actb actin, beta gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14661057 735802 Actb actin, beta gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17877786 735802 Actb actin, beta gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17877786 735802 Actb actin, beta gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17877786 735802 Actb actin, beta gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15254588 735802 Actb actin, beta gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17877786 735802 Actb actin, beta gene MP:0006325 impaired hearing IAGP N RGD:5509061 20181122 MGI PMID:30012594 735802 Actb actin, beta gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:23544080 735802 Actb actin, beta gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:23544080 735802 Actb actin, beta gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:23544080 735802 Actb actin, beta gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20150101 MGI PMID:23185019 735802 Actb actin, beta gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17877786 735802 Actb actin, beta gene MP:0009342 enlarged gallbladder IAGP N RGD:5509061 20141003 MGI PMID:14661057 735802 Actb actin, beta gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15254588 735802 Actb actin, beta gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20976199 735802 Actb actin, beta gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9635195 735802 Actb actin, beta gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18308728 735802 Actb actin, beta gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14661057 735802 Actb actin, beta gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16028230 735802 Actb actin, beta gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9608737 735802 Actb actin, beta gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17877786 735802 Actb actin, beta gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17877786 735802 Actb actin, beta gene MP:0011939 increased food intake IAGP N RGD:5509061 20190815 MGI PMID:17877786 735802 Actb actin, beta gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20976199 735802 Actb actin, beta gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20190815 MGI PMID:17877786 735802 Actb actin, beta gene MP:0030968 decreased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:17877786 735804 Clic6 chloride intracellular channel 6 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20231207 MGI 735804 Clic6 chloride intracellular channel 6 gene MP:0001486 abnormal startle reflex IEA N RGD:5509061 20231207 MGI 735805 Atp2b3 ATPase, Ca++ transporting, plasma membrane 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 735805 Atp2b3 ATPase, Ca++ transporting, plasma membrane 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 735805 Atp2b3 ATPase, Ca++ transporting, plasma membrane 3 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 735805 Atp2b3 ATPase, Ca++ transporting, plasma membrane 3 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20231207 MGI 735805 Atp2b3 ATPase, Ca++ transporting, plasma membrane 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:15199144 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15199144 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23622066 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23622066 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23622066 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001588 abnormal hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:17431400 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15199144 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:23622066 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:23622066 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0002637 small uterus IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15199144 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:23622066 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0003948 abnormal gas homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:23622066 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15199144 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:15199144 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0008319 abnormal sympathetic afferent fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:23622066 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:23622066 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23622066 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0008963 increased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0008983 small vagina IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0009015 short proestrus IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0009018 short estrus IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0009209 abnormal internal female genitalia morphology IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0009287 decreased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0010073 decreased pruritus IAGP N RGD:5509061 20141003 MGI PMID:23622066 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20160414 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0014169 decreased brown adipose tissue mass IAGP N RGD:5509061 20160414 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:17431400 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220512 MGI PMID:18174360 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0031270 decreased susceptibility to age-related hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:20864514 735810 Nr2c2 nuclear receptor subfamily 2, group C, member 2 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:18174360 735812 Otop1 otopetrin 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 735812 Otop1 otopetrin 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 735812 Otop1 otopetrin 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 735812 Otop1 otopetrin 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20230601 MGI 735812 Otop1 otopetrin 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15730345 735812 Otop1 otopetrin 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:15730345 735812 Otop1 otopetrin 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:12651873 735812 Otop1 otopetrin 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:15109702 735812 Otop1 otopetrin 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:15730345 735812 Otop1 otopetrin 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:20554841 735812 Otop1 otopetrin 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:9714575 735812 Otop1 otopetrin 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20160204 MGI PMID:16972005 735812 Otop1 otopetrin 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:15730345 735812 Otop1 otopetrin 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12651873 735812 Otop1 otopetrin 1 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:15730345 735812 Otop1 otopetrin 1 gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12524184 735812 Otop1 otopetrin 1 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:12651873 735812 Otop1 otopetrin 1 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:15109702 735812 Otop1 otopetrin 1 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:15730345 735812 Otop1 otopetrin 1 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:20554841 735812 Otop1 otopetrin 1 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:9714575 735812 Otop1 otopetrin 1 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:20554841 735812 Otop1 otopetrin 1 gene MP:0004813 absent linear vestibular evoked potential IAGP N RGD:5509061 20141003 MGI PMID:15109702 735812 Otop1 otopetrin 1 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:12651873 735812 Otop1 otopetrin 1 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:15730345 735812 Otop1 otopetrin 1 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:9714575 735812 Otop1 otopetrin 1 gene MP:0005191 head tilt IAGP N RGD:5509061 20160204 MGI PMID:16972005 735812 Otop1 otopetrin 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 735814 Kcnn1 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20230601 MGI 735814 Kcnn1 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20230601 MGI 735814 Kcnn1 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 735816 Slc22a3 solute carrier family 22 (organic cation transporter), member 3 gene MP:0001293 anophthalmia IEA N RGD:5509061 20201022 MGI 735816 Slc22a3 solute carrier family 22 (organic cation transporter), member 3 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 735816 Slc22a3 solute carrier family 22 (organic cation transporter), member 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 735816 Slc22a3 solute carrier family 22 (organic cation transporter), member 3 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 735816 Slc22a3 solute carrier family 22 (organic cation transporter), member 3 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22143804 735816 Slc22a3 solute carrier family 22 (organic cation transporter), member 3 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20201022 MGI 735816 Slc22a3 solute carrier family 22 (organic cation transporter), member 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 735816 Slc22a3 solute carrier family 22 (organic cation transporter), member 3 gene MP:0011451 increased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:22143804 735816 Slc22a3 solute carrier family 22 (organic cation transporter), member 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 735818 Egr4 early growth response 4 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20220623 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0008893 detached sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10529423 735818 Egr4 early growth response 4 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:10529423 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20201015 MGI PMID:30989113 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20240523 MGI 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20240523 MGI 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20201015 MGI PMID:30989113 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20201015 MGI PMID:30989113 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20201015 MGI PMID:30989113 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20201015 MGI PMID:30989113 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20201015 MGI PMID:30989113 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20201015 MGI PMID:30989113 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20201015 MGI PMID:30989113 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20201015 MGI PMID:30989113 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20201015 MGI PMID:30989113 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20201015 MGI PMID:30989113 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20201015 MGI PMID:30989113 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20201015 MGI PMID:30989113 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20201015 MGI PMID:30989113 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20201015 MGI PMID:30989113 735820 Ralgapa1 Ral GTPase activating protein, alpha subunit 1 gene MP:0030022 decreased muscle cell glucose uptake IAGP N RGD:5509061 20201015 MGI PMID:30989113 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11279075 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12569166 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:9139827 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12569166 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16469807 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0001304 cataract IEA N RGD:5509061 20220811 MGI 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0001777 abnormal body temperature homeostasis IEA N RGD:5509061 20111116 MGI 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12569166 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12569166 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0002608 increased hematocrit IEA N RGD:5509061 20231207 MGI 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12569166 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12569166 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20211021 MGI 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0003829 impaired febrile response IAGP N RGD:5509061 20240307 MGI PMID:33944778 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0004122 abnormal sinus arrhythmia IEA N RGD:5509061 20211021 MGI 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0004156 abnormal QT variability IEA N RGD:5509061 20220519 MGI 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0005288 abnormal oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:9139827 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:16469807 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:10748195 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:12569166 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:12569166 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:12569166 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:12569166 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:9139827 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:10497167 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:11279075 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9139827 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20210422 MGI PMID:33177714 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:12569166 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:16469807 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:11279075 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:16469807 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:9139827 735822 Ucp1 uncoupling protein 1 (mitochondrial, proton carrier) gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20180111 MGI PMID:22961106 735825 Prss1 serine protease 1 (trypsin 1) gene MP:0000274 enlarged heart IEA N RGD:5509061 20170105 MGI 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17923534 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:17923534 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:16186258 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17923534 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:17923534 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17923534 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:17923534 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16186258 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:17923534 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17923534 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:17923534 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:17923534 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:17923534 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17923534 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:17923534 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:17923534 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17923534 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16186258 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16186258 735829 Lin7c lin-7 homolog C, crumbs cell polarity complex component gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17923534 735831 Ccng1 cyclin G1 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:11423978 735831 Ccng1 cyclin G1 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:11423978 735831 Ccng1 cyclin G1 gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:11423978 735831 Ccng1 cyclin G1 gene MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:12668979 735831 Ccng1 cyclin G1 gene MP:0002658 abnormal liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:12668979 735831 Ccng1 cyclin G1 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:12668979 735831 Ccng1 cyclin G1 gene MP:0010264 increased hepatoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12668979 735831 Ccng1 cyclin G1 gene MP:0010265 decreased hepatoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12668979 735836 Kcnip3 Kv channel interacting protein 3, calsenilin gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19223600 735836 Kcnip3 Kv channel interacting protein 3, calsenilin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:14534243 735836 Kcnip3 Kv channel interacting protein 3, calsenilin gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:14534243 735836 Kcnip3 Kv channel interacting protein 3, calsenilin gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11792319 735836 Kcnip3 Kv channel interacting protein 3, calsenilin gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:11792319 735836 Kcnip3 Kv channel interacting protein 3, calsenilin gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:11792319 735836 Kcnip3 Kv channel interacting protein 3, calsenilin gene MP:0002764 short tibia IEA N RGD:5509061 20211021 MGI 735836 Kcnip3 Kv channel interacting protein 3, calsenilin gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:14534243 735836 Kcnip3 Kv channel interacting protein 3, calsenilin gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:11792319 735836 Kcnip3 Kv channel interacting protein 3, calsenilin gene MP:0003484 abnormal channel response IAGP N RGD:5509061 20141003 MGI PMID:14534243 735836 Kcnip3 Kv channel interacting protein 3, calsenilin gene MP:0005316 abnormal response to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:14534243 735836 Kcnip3 Kv channel interacting protein 3, calsenilin gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11792319 735836 Kcnip3 Kv channel interacting protein 3, calsenilin gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20141003 MGI PMID:14534243 735836 Kcnip3 Kv channel interacting protein 3, calsenilin gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11792319 735836 Kcnip3 Kv channel interacting protein 3, calsenilin gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19223600 735838 Gak cyclin G associated kinase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20240523 MGI 735838 Gak cyclin G associated kinase gene MP:0000274 enlarged heart IEA N RGD:5509061 20240523 MGI 735838 Gak cyclin G associated kinase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0000627 abnormal mammary gland morphology IEA N RGD:5509061 20240523 MGI 735838 Gak cyclin G associated kinase gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20240523 MGI 735838 Gak cyclin G associated kinase gene MP:0000691 enlarged spleen IEA N RGD:5509061 20240523 MGI 735838 Gak cyclin G associated kinase gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20240523 MGI 735838 Gak cyclin G associated kinase gene MP:0000709 enlarged thymus IEA N RGD:5509061 20240523 MGI 735838 Gak cyclin G associated kinase gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20240523 MGI 735838 Gak cyclin G associated kinase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20240523 MGI 735838 Gak cyclin G associated kinase gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0003068 enlarged kidney IEA N RGD:5509061 20240523 MGI 735838 Gak cyclin G associated kinase gene MP:0003917 increased kidney weight IEA N RGD:5509061 20240523 MGI 735838 Gak cyclin G associated kinase gene MP:0003950 abnormal plasma membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20141003 MGI PMID:22022498 735838 Gak cyclin G associated kinase gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20240523 MGI 735838 Gak cyclin G associated kinase gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0010900 abnormal pulmonary interalveolar septum morphology IAGP N RGD:5509061 20141003 MGI PMID:22022498 735838 Gak cyclin G associated kinase gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20141003 MGI PMID:22022498 735838 Gak cyclin G associated kinase gene MP:0010995 abnormal lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:22022498 735838 Gak cyclin G associated kinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22022498 735838 Gak cyclin G associated kinase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18434600 735838 Gak cyclin G associated kinase gene MP:0012242 abnormal hepatoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:18434600 735840 Cox4i2 cytochrome c oxidase subunit 4I2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:22730437 735840 Cox4i2 cytochrome c oxidase subunit 4I2 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:22730437 735840 Cox4i2 cytochrome c oxidase subunit 4I2 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:22730437 735840 Cox4i2 cytochrome c oxidase subunit 4I2 gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:22730437 735840 Cox4i2 cytochrome c oxidase subunit 4I2 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:22730437 735840 Cox4i2 cytochrome c oxidase subunit 4I2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22730437 735840 Cox4i2 cytochrome c oxidase subunit 4I2 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22730437 735840 Cox4i2 cytochrome c oxidase subunit 4I2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:22730437 735840 Cox4i2 cytochrome c oxidase subunit 4I2 gene MP:0031252 abnormal physiological response to hypoxia IAGP N RGD:5509061 20210729 MGI PMID:31848220 735846 Cacng6 calcium channel, voltage-dependent, gamma subunit 6 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0000264 failure of vascular branching IAGP N RGD:5509061 20141003 MGI PMID:12354787 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20180712 MGI PMID:22834956 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20180712 MGI PMID:22834956 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:12354787 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0000785 telencephalon hypoplasia IAGP N RGD:5509061 20180712 MGI PMID:22834956 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:20371803 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0000844 abnormal pontine flexure morphology IAGP N RGD:5509061 20141003 MGI PMID:12354787 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20220127 MGI PMID:32385775 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:12354787 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12354787 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20180712 MGI PMID:22834956 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:12354787 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0001725 abnormal umbilical cord morphology IAGP N RGD:5509061 20141003 MGI PMID:12354787 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0001727 abnormal embryo implantation IAGP N RGD:5509061 20220127 MGI PMID:32385775 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20220127 MGI PMID:32385775 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18635581 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20371803 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220127 MGI PMID:32385775 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0001926 female infertility IAGP N RGD:5509061 20220127 MGI PMID:32385775 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220127 MGI PMID:32385775 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20180712 MGI PMID:22834956 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20156974 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18635581 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12354787 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20180712 MGI PMID:22834956 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20371803 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20180712 MGI PMID:22834956 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12354787 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:12354787 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0003815 hairless IAGP N RGD:5509061 20180712 MGI PMID:22834956 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20220127 MGI PMID:32385775 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20180712 MGI PMID:22834956 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20371803 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:18635581 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:20644114 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20220127 MGI PMID:32385775 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:12354787 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20180712 MGI PMID:22834956 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12354787 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18635581 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0008173 increased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:20156974 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:20156974 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20220127 MGI PMID:32385775 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0009664 abnormal luminal closure IAGP N RGD:5509061 20220127 MGI PMID:32385775 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0009667 abnormal embryo invasion IAGP N RGD:5509061 20220127 MGI PMID:32385775 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0009922 increased transitional stage T1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:20156974 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0009926 decreased transitional stage T2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:20156974 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22042698 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20371803 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12354787 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18635581 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20180712 MGI PMID:22834956 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20644114 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0012022 increased melanocyte number IAGP N RGD:5509061 20180712 MGI PMID:22834956 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0012082 delayed heart development IAGP N RGD:5509061 20141003 MGI PMID:12354787 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0012254 absent intersomitic vessels IAGP N RGD:5509061 20141003 MGI PMID:12354787 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0012728 abnormal somite border morphology IAGP N RGD:5509061 20180712 MGI PMID:22834956 735848 Adam10 a disintegrin and metallopeptidase domain 10 gene MP:0013577 forestomach hypoplasia IAGP N RGD:5509061 20150305 MGI PMID:22764128 735853 Homer3 homer scaffolding protein 3 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:22561452 735860 Slit3 slit guidance ligand 3 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:14550534 735860 Slit3 slit guidance ligand 3 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:14550534 735860 Slit3 slit guidance ligand 3 gene MP:0000757 herniated abdominal wall IEA N RGD:5509061 20150430 MGI 735860 Slit3 slit guidance ligand 3 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:12702769 735860 Slit3 slit guidance ligand 3 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:12702769 735860 Slit3 slit guidance ligand 3 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12702769 735860 Slit3 slit guidance ligand 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12702769 735860 Slit3 slit guidance ligand 3 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:24355925 735860 Slit3 slit guidance ligand 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12702769 735860 Slit3 slit guidance ligand 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12702769 735860 Slit3 slit guidance ligand 3 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:14550534 735860 Slit3 slit guidance ligand 3 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:12702769 735860 Slit3 slit guidance ligand 3 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:24355925 735860 Slit3 slit guidance ligand 3 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15091338 735860 Slit3 slit guidance ligand 3 gene MP:0003270 intestinal obstruction IAGP N RGD:5509061 20141003 MGI PMID:12702769 735860 Slit3 slit guidance ligand 3 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14550534 735860 Slit3 slit guidance ligand 3 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:12702769 735860 Slit3 slit guidance ligand 3 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:14550534 735860 Slit3 slit guidance ligand 3 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:24355925 735860 Slit3 slit guidance ligand 3 gene MP:0005155 herniated intestine IAGP N RGD:5509061 20141003 MGI PMID:12702769 735860 Slit3 slit guidance ligand 3 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18829537 735860 Slit3 slit guidance ligand 3 gene MP:0009678 abnormal spinal cord lateral column morphology IAGP N RGD:5509061 20141003 MGI PMID:15091338 735860 Slit3 slit guidance ligand 3 gene MP:0009695 abnormal spinal cord ventral commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:15091338 735860 Slit3 slit guidance ligand 3 gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:12702769 735860 Slit3 slit guidance ligand 3 gene MP:0010173 increased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18829537 735860 Slit3 slit guidance ligand 3 gene MP:0010402 ventricular septal defect IEA N RGD:5509061 20150430 MGI 735860 Slit3 slit guidance ligand 3 gene MP:0010912 herniated liver IAGP N RGD:5509061 20141003 MGI PMID:12702769 735860 Slit3 slit guidance ligand 3 gene MP:0011660 ectopia cordis IEA N RGD:5509061 20150430 MGI 735860 Slit3 slit guidance ligand 3 gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20150430 MGI 735860 Slit3 slit guidance ligand 3 gene MP:0011668 double outlet right ventricle, Taussig bing type IEA N RGD:5509061 20150430 MGI 735860 Slit3 slit guidance ligand 3 gene MP:0011682 renal glomerulus cyst IEA N RGD:5509061 20150806 MGI 735860 Slit3 slit guidance ligand 3 gene MP:0012061 abnormal diaphragm central tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:12702769 735860 Slit3 slit guidance ligand 3 gene MP:0012061 abnormal diaphragm central tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:24355925 735860 Slit3 slit guidance ligand 3 gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20141003 MGI PMID:12702769 735860 Slit3 slit guidance ligand 3 gene MP:0014518 myocardial hypertrabeculation IEA N RGD:5509061 20240822 MGI 735860 Slit3 slit guidance ligand 3 gene MP:0030786 absent falciform ligament IAGP N RGD:5509061 20181004 MGI PMID:12702769 735862 Nptxr neuronal pentraxin receptor gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:16763034 735864 Kcng3 potassium voltage-gated channel, subfamily G, member 3 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20231207 MGI 735867 Slc6a15 solute carrier family 6 (neurotransmitter transporter), member 15 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17931606 735867 Slc6a15 solute carrier family 6 (neurotransmitter transporter), member 15 gene MP:0011886 increased circulating lipase level IEA N RGD:5509061 20211021 MGI 735870 Acadsb acyl-Coenzyme A dehydrogenase, short/branched chain gene MP:0000452 abnormal mouth morphology IEA N RGD:5509061 20230601 MGI 735870 Acadsb acyl-Coenzyme A dehydrogenase, short/branched chain gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 735870 Acadsb acyl-Coenzyme A dehydrogenase, short/branched chain gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 735870 Acadsb acyl-Coenzyme A dehydrogenase, short/branched chain gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20230601 MGI 735870 Acadsb acyl-Coenzyme A dehydrogenase, short/branched chain gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20230601 MGI 735870 Acadsb acyl-Coenzyme A dehydrogenase, short/branched chain gene MP:0004222 iris synechia IEA N RGD:5509061 20230601 MGI 735870 Acadsb acyl-Coenzyme A dehydrogenase, short/branched chain gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210826 MGI 735875 Fxyd4 FXYD domain-containing ion transport regulator 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12167609 735875 Fxyd4 FXYD domain-containing ion transport regulator 4 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:12167609 735875 Fxyd4 FXYD domain-containing ion transport regulator 4 gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12167609 735875 Fxyd4 FXYD domain-containing ion transport regulator 4 gene MP:0002847 abnormal renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:12167609 735875 Fxyd4 FXYD domain-containing ion transport regulator 4 gene MP:0005627 increased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:12167609 735875 Fxyd4 FXYD domain-containing ion transport regulator 4 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:12167609 735875 Fxyd4 FXYD domain-containing ion transport regulator 4 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:12167609 735879 Ache acetylcholinesterase gene MP:0000054 delayed ear emergence IAGP N RGD:5509061 20141003 MGI PMID:10869390 735879 Ache acetylcholinesterase gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 735879 Ache acetylcholinesterase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 735879 Ache acetylcholinesterase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10869390 735879 Ache acetylcholinesterase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17038428 735879 Ache acetylcholinesterase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:18322091 735879 Ache acetylcholinesterase gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:16289062 735879 Ache acetylcholinesterase gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:16289062 735879 Ache acetylcholinesterase gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:18322091 735879 Ache acetylcholinesterase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10869390 735879 Ache acetylcholinesterase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18977317 735879 Ache acetylcholinesterase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19357277 735879 Ache acetylcholinesterase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16289062 735879 Ache acetylcholinesterase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19357277 735879 Ache acetylcholinesterase gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:10869390 735879 Ache acetylcholinesterase gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 735879 Ache acetylcholinesterase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10869390 735879 Ache acetylcholinesterase gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:10869390 735879 Ache acetylcholinesterase gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:19357277 735879 Ache acetylcholinesterase gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:19357277 735879 Ache acetylcholinesterase gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10869390 735879 Ache acetylcholinesterase gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:16289062 735879 Ache acetylcholinesterase gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:19357277 735879 Ache acetylcholinesterase gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17038428 735879 Ache acetylcholinesterase gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19357277 735879 Ache acetylcholinesterase gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17038428 735879 Ache acetylcholinesterase gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 735879 Ache acetylcholinesterase gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:16289062 735879 Ache acetylcholinesterase gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:19357277 735879 Ache acetylcholinesterase gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:18977317 735879 Ache acetylcholinesterase gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16289062 735879 Ache acetylcholinesterase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17038428 735879 Ache acetylcholinesterase gene MP:0002188 small heart IEA N RGD:5509061 20210128 MGI 735879 Ache acetylcholinesterase gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20141003 MGI PMID:18977317 735879 Ache acetylcholinesterase gene MP:0003492 abnormal involuntary movement IAGP N RGD:5509061 20141003 MGI PMID:19357277 735879 Ache acetylcholinesterase gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:17038428 735879 Ache acetylcholinesterase gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20141003 MGI PMID:10869390 735879 Ache acetylcholinesterase gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:18322091 735879 Ache acetylcholinesterase gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:17038428 735879 Ache acetylcholinesterase gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:18977317 735879 Ache acetylcholinesterase gene MP:0005575 increased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:18977317 735879 Ache acetylcholinesterase gene MP:0005576 decreased pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:18977317 735879 Ache acetylcholinesterase gene MP:0005585 increased tidal volume IAGP N RGD:5509061 20141003 MGI PMID:18977317 735879 Ache acetylcholinesterase gene MP:0005586 decreased tidal volume IAGP N RGD:5509061 20141003 MGI PMID:18977317 735879 Ache acetylcholinesterase gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17038428 735879 Ache acetylcholinesterase gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:10869390 735879 Ache acetylcholinesterase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17038428 735879 Ache acetylcholinesterase gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17194517 735879 Ache acetylcholinesterase gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17194517 735879 Ache acetylcholinesterase gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18977317 735879 Ache acetylcholinesterase gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17194517 735879 Ache acetylcholinesterase gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:16289062 735879 Ache acetylcholinesterase gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19357277 735879 Ache acetylcholinesterase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10869390 735879 Ache acetylcholinesterase gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10869390 735879 Ache acetylcholinesterase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 735879 Ache acetylcholinesterase gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:16289062 735881 Reln reelin gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 735881 Reln reelin gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 735881 Reln reelin gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20201022 MGI 735881 Reln reelin gene MP:0000743 muscle spasm IEA N RGD:5509061 20111116 MGI 735881 Reln reelin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12399118 735881 Reln reelin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:1557392 735881 Reln reelin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:7972007 735881 Reln reelin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9205121 735881 Reln reelin gene MP:0000745 tremors IAGP N RGD:5509061 20200123 MGI PMID:24539699 735881 Reln reelin gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7127145 735881 Reln reelin gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20160616 MGI PMID:25788693 735881 Reln reelin gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:12399118 735881 Reln reelin gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:23968836 735881 Reln reelin gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:7127145 735881 Reln reelin gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:11830577 735881 Reln reelin gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:15249135 735881 Reln reelin gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20160616 MGI PMID:25788693 735881 Reln reelin gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:12399118 735881 Reln reelin gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15249135 735881 Reln reelin gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20160616 MGI PMID:25788693 735881 Reln reelin gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:11830577 735881 Reln reelin gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:12399118 735881 Reln reelin gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20160616 MGI PMID:25788693 735881 Reln reelin gene MP:0000813 abnormal hippocampus layer morphology IEA N RGD:5509061 20111116 MGI 735881 Reln reelin gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 735881 Reln reelin gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20150702 MGI PMID:7127145 735881 Reln reelin gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:10876649 735881 Reln reelin gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:1557392 735881 Reln reelin gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:7972007 735881 Reln reelin gene MP:0000852 small cerebellum IAGP N RGD:5509061 20150702 MGI PMID:7127145 735881 Reln reelin gene MP:0000853 absent cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:7972007 735881 Reln reelin gene MP:0000854 abnormal cerebellum development IEA N RGD:5509061 20111116 MGI 735881 Reln reelin gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:1557392 735881 Reln reelin gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:12399118 735881 Reln reelin gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:10876649 735881 Reln reelin gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1557392 735881 Reln reelin gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:10876649 735881 Reln reelin gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:1557392 735881 Reln reelin gene MP:0000884 delaminated Purkinje cell layer IEA N RGD:5509061 20111116 MGI 735881 Reln reelin gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:1557392 735881 Reln reelin gene MP:0000886 abnormal cerebellar granule layer morphology IEA N RGD:5509061 20111116 MGI 735881 Reln reelin gene MP:0000887 delaminated cerebellar granule layer IEA N RGD:5509061 20111116 MGI 735881 Reln reelin gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20201022 MGI 735881 Reln reelin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12399118 735881 Reln reelin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:1557392 735881 Reln reelin gene MP:0001265 decreased body size IAGP N RGD:5509061 20200123 MGI PMID:24539699 735881 Reln reelin gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20151022 MGI PMID:25845740 735881 Reln reelin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12399118 735881 Reln reelin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:1557392 735881 Reln reelin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:7972007 735881 Reln reelin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12399118 735881 Reln reelin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20200123 MGI PMID:24539699 735881 Reln reelin gene MP:0001405 impaired coordination IEA N RGD:5509061 20141003 MGI 735881 Reln reelin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:7972007 735881 Reln reelin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20200123 MGI PMID:24539699 735881 Reln reelin gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:7972007 735881 Reln reelin gene MP:0001511 disheveled coat IAGP N RGD:5509061 20200123 MGI PMID:24539699 735881 Reln reelin gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:12399118 735881 Reln reelin gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:9205121 735881 Reln reelin gene MP:0001525 impaired balance IAGP N RGD:5509061 20200123 MGI PMID:24539699 735881 Reln reelin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12399118 735881 Reln reelin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200123 MGI PMID:24539699 735881 Reln reelin gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20200123 MGI PMID:24539699 735881 Reln reelin gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0001925 male infertility IAGP N RGD:5509061 20200123 MGI PMID:24539699 735881 Reln reelin gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 735881 Reln reelin gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 735881 Reln reelin gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20111116 MGI 735881 Reln reelin gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12399118 735881 Reln reelin gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20201022 MGI 735881 Reln reelin gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20160915 MGI PMID:8352721 735881 Reln reelin gene MP:0003088 abnormal prepulse inhibition IAGP N RGD:5509061 20151022 MGI PMID:25845740 735881 Reln reelin gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:21214893 735881 Reln reelin gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11580894 735881 Reln reelin gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11580894 735881 Reln reelin gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11580894 735881 Reln reelin gene MP:0004097 abnormal cerebellar cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:7972007 735881 Reln reelin gene MP:0004103 abnormal ventral striatum morphology IAGP N RGD:5509061 20150924 MGI PMID:11982630 735881 Reln reelin gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 735881 Reln reelin gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 735881 Reln reelin gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0005267 abnormal olfactory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:7127145 735881 Reln reelin gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11580894 735881 Reln reelin gene MP:0006300 abnormal entorhinal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0008031 decreased Cajal-Retzius cell number IAGP N RGD:5509061 20141003 MGI PMID:19805388 735881 Reln reelin gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20160616 MGI PMID:25788693 735881 Reln reelin gene MP:0008265 abnormal hippocampus CA2 region morphology IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:11830577 735881 Reln reelin gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:7972007 735881 Reln reelin gene MP:0008285 abnormal hippocampus granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:7972007 735881 Reln reelin gene MP:0008431 abnormal short-term spatial reference memory IAGP N RGD:5509061 20151022 MGI PMID:25845740 735881 Reln reelin gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:4644329 735881 Reln reelin gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:1557392 735881 Reln reelin gene MP:0009709 hydrometra IEA N RGD:5509061 20201022 MGI 735881 Reln reelin gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20150702 MGI PMID:7127145 735881 Reln reelin gene MP:0009949 abnormal olfactory bulb granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17494763 735881 Reln reelin gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20200123 MGI PMID:24539699 735881 Reln reelin gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 735881 Reln reelin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 735881 Reln reelin gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20150924 MGI PMID:11982630 735884 Entpd2 ectonucleoside triphosphate diphosphohydrolase 2 gene MP:0001985 abnormal gustatory system physiology IAGP N RGD:5509061 20141003 MGI PMID:23959882 735884 Entpd2 ectonucleoside triphosphate diphosphohydrolase 2 gene MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:23959882 735884 Entpd2 ectonucleoside triphosphate diphosphohydrolase 2 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:23959882 735884 Entpd2 ectonucleoside triphosphate diphosphohydrolase 2 gene MP:0006260 abnormal gustatory papilla taste bud morphology IAGP N RGD:5509061 20141003 MGI PMID:23959882 735889 Amacr alpha-methylacyl-CoA racemase gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15016763 735889 Amacr alpha-methylacyl-CoA racemase gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:15016763 735889 Amacr alpha-methylacyl-CoA racemase gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:15016763 735889 Amacr alpha-methylacyl-CoA racemase gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:15016763 735889 Amacr alpha-methylacyl-CoA racemase gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:15016763 735889 Amacr alpha-methylacyl-CoA racemase gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15016763 735889 Amacr alpha-methylacyl-CoA racemase gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:15016763 735889 Amacr alpha-methylacyl-CoA racemase gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15016763 735889 Amacr alpha-methylacyl-CoA racemase gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15016763 735889 Amacr alpha-methylacyl-CoA racemase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15016763 735889 Amacr alpha-methylacyl-CoA racemase gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:15016763 735894 Muc4 mucin 4 gene MP:0001262 decreased body weight IEA N RGD:5509061 20200528 MGI 735894 Muc4 mucin 4 gene MP:0001954 respiratory distress IEA N RGD:5509061 20200528 MGI 735894 Muc4 mucin 4 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20170406 MGI PMID:26364605 735894 Muc4 mucin 4 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20170406 MGI PMID:26364605 735894 Muc4 mucin 4 gene MP:0013299 decreased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20170406 MGI PMID:26364605 735894 Muc4 mucin 4 gene MP:0020185 abnormal susceptibility to viral infection IEA N RGD:5509061 20200528 MGI 735894 Muc4 mucin 4 gene MP:0020940 increased susceptibility to Togaviridae infection IEA N RGD:5509061 20200604 MGI 735894 Muc4 mucin 4 gene MP:0020949 increased susceptibility to Coronaviridae infection IEA N RGD:5509061 20200604 MGI 735894 Muc4 mucin 4 gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IEA N RGD:5509061 20200604 MGI 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000370 head blaze IAGP N RGD:5509061 20150827 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000370 head blaze IAGP N RGD:5509061 20150827 MGI PMID:3855546 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20150827 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:15493017 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:16245023 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:17699610 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:18397875 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:23382688 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000373 belly spot IAGP N RGD:5509061 20150827 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000373 belly spot IAGP N RGD:5509061 20150827 MGI PMID:3855546 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000373 belly spot IAGP N RGD:5509061 20180517 MGI PMID:29361054 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000373 belly spot IAGP N RGD:5509061 20181122 MGI PMID:28431046 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000373 belly spot IAGP N RGD:5509061 20230427 MGI PMID:16586440 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20141003 MGI PMID:16790476 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:17028340 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20170601 MGI PMID:8631507 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20170601 MGI PMID:8631507 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20170601 MGI PMID:8631507 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:23382688 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20457761 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000745 tremors IAGP N RGD:5509061 20150827 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000745 tremors IAGP N RGD:5509061 20150827 MGI PMID:3855546 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:23643381 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:20457761 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20150827 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000921 demyelination IAGP N RGD:5509061 20150827 MGI PMID:3855546 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:18773073 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20150827 MGI PMID:3855546 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20144603 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:20187849 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20170601 MGI PMID:9425902 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16790476 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20144603 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001025 abnormal sympathetic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20144603 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001034 abnormal parasympathetic ganglion morphology IAGP N RGD:5509061 20170601 MGI PMID:8631507 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:20144603 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20170601 MGI PMID:20739296 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20170601 MGI PMID:20739296 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16790476 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17699610 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20170601 MGI PMID:9425902 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001087 abnormal nodose ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001105 abnormal PNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17699610 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20457761 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20180517 MGI PMID:29361054 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001108 absent Schwann cells IAGP N RGD:5509061 20180517 MGI PMID:29361054 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001189 absent skin pigmentation IAGP N RGD:5509061 20150827 MGI PMID:3855546 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20457761 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23382688 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:20457761 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20457761 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20457761 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20150827 MGI PMID:3855546 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16790476 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20457761 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002064 seizures IAGP N RGD:5509061 20150827 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15493017 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20457761 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002083 premature death IAGP N RGD:5509061 20150827 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002083 premature death IAGP N RGD:5509061 20150827 MGI PMID:3855546 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:20187849 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17699610 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002183 gliosis IAGP N RGD:5509061 20150827 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20457761 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20150827 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002654 spongiform encephalopathy IAGP N RGD:5509061 20150827 MGI PMID:3855546 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002671 belted IAGP N RGD:5509061 20141003 MGI PMID:18397875 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:15493017 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:20187849 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:6512238 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002731 megacolon IAGP N RGD:5509061 20150827 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002731 megacolon IAGP N RGD:5509061 20180517 MGI PMID:29361054 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:20187849 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20141003 MGI PMID:15843399 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20141003 MGI PMID:17699610 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20170601 MGI PMID:20739296 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002926 aganglionic megacolon IAGP N RGD:5509061 20230427 MGI PMID:16586440 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002938 white spotting IAGP N RGD:5509061 20170601 MGI PMID:8631507 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002939 head spot IAGP N RGD:5509061 20181122 MGI PMID:28431046 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002940 variable body spotting IAGP N RGD:5509061 20141003 MGI PMID:6512238 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20170601 MGI PMID:9425902 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:23643381 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20457761 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20180517 MGI PMID:29361054 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23643381 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:20457761 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0004493 dilated cochlea IAGP N RGD:5509061 20230420 MGI PMID:36343245 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16790476 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20150827 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0005175 non-pigmented tail tip IAGP N RGD:5509061 20150827 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:20457761 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:23643381 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:10077527 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:18397875 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:18773073 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:23382688 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20230427 MGI PMID:16586440 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0005409 darkened coat color IAGP N RGD:5509061 20150827 MGI PMID:3855546 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0006408 dorsal root ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17699610 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0006408 dorsal root ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20144603 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20150827 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0008289 abnormal adrenal medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:20144603 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0008492 dorsal root ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:20457761 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20180517 MGI PMID:29361054 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:20144603 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:23643381 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:20187849 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:16790476 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:20144603 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:23382688 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20181122 MGI PMID:28431046 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0009784 abnormal melanoblast migration IAGP N RGD:5509061 20141003 MGI PMID:17699610 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:16790476 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20141003 MGI PMID:17699610 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0009808 decreased oligodendrocyte number IAGP N RGD:5509061 20240425 MGI PMID:35137157 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0009846 abnormal neural crest morphology IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:20457761 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6512238 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16790476 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17699610 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20187849 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20150827 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20144603 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180517 MGI PMID:29361054 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17699610 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15493017 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:6512238 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18773073 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15493017 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18773073 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18773073 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18773073 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011266 abnormal frontonasal mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:23643381 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011277 decreased tail pigmentation IEA N RGD:5509061 20141003 MGI 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011568 decreased foot pigmentation IAGP N RGD:5509061 20170810 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20141003 MGI PMID:23643381 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0011904 abnormal Schwann cell physiology IAGP N RGD:5509061 20180517 MGI PMID:29361054 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20141003 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20150827 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0012745 abnormal neural crest cell physiology IAGP N RGD:5509061 20170601 MGI PMID:20739296 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0013001 abnormal enteric neural crest cell morphology IAGP N RGD:5509061 20170601 MGI PMID:20739296 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0013003 absent enteric neural crest cell IAGP N RGD:5509061 20181220 MGI PMID:11156606 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0013006 abnormal enteric neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:16790476 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0013007 abnormal vagal neural crest cell migration IAGP N RGD:5509061 20170601 MGI PMID:8631507 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0013009 increased vagal neural crest cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16790476 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20151217 MGI PMID:25399070 735897 Sox10 SRY (sex determining region Y)-box 10 gene MP:0030908 abnormal melanocyte differentiation IAGP N RGD:5509061 20181220 MGI PMID:9425902 735898 Gls2 glutaminase 2 (liver, mitochondrial) gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210826 MGI 735898 Gls2 glutaminase 2 (liver, mitochondrial) gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20210128 MGI 735898 Gls2 glutaminase 2 (liver, mitochondrial) gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20220519 MGI 735898 Gls2 glutaminase 2 (liver, mitochondrial) gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210826 MGI 735898 Gls2 glutaminase 2 (liver, mitochondrial) gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210826 MGI 735898 Gls2 glutaminase 2 (liver, mitochondrial) gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 735898 Gls2 glutaminase 2 (liver, mitochondrial) gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20220519 MGI 735898 Gls2 glutaminase 2 (liver, mitochondrial) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 735898 Gls2 glutaminase 2 (liver, mitochondrial) gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20210513 MGI PMID:29578539 735898 Gls2 glutaminase 2 (liver, mitochondrial) gene MP:0005505 thrombocytosis IEA N RGD:5509061 20231207 MGI 735898 Gls2 glutaminase 2 (liver, mitochondrial) gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20210513 MGI PMID:29578539 735898 Gls2 glutaminase 2 (liver, mitochondrial) gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20220519 MGI 735898 Gls2 glutaminase 2 (liver, mitochondrial) gene MP:0013278 decreased fasting circulating glucose level IAGP N RGD:5509061 20210513 MGI PMID:29578539 735898 Gls2 glutaminase 2 (liver, mitochondrial) gene MP:0020103 decreased hepatic glucose production IAGP N RGD:5509061 20210513 MGI PMID:29578539 735898 Gls2 glutaminase 2 (liver, mitochondrial) gene MP:0030709 increased circulating glutamine level IAGP N RGD:5509061 20210513 MGI PMID:29578539 735901 Nrxn2 neurexin II gene MP:0000274 enlarged heart IEA N RGD:5509061 20201022 MGI 735901 Nrxn2 neurexin II gene MP:0000745 tremors IEA N RGD:5509061 20201231 MGI 735901 Nrxn2 neurexin II gene MP:0001262 decreased body weight IEA N RGD:5509061 20111116 MGI 735901 Nrxn2 neurexin II gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20150507 MGI PMID:25423136 735901 Nrxn2 neurexin II gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20150507 MGI PMID:25423136 735901 Nrxn2 neurexin II gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 735901 Nrxn2 neurexin II gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 735901 Nrxn2 neurexin II gene MP:0001406 abnormal gait IEA N RGD:5509061 20201231 MGI 735901 Nrxn2 neurexin II gene MP:0001512 trunk curl IEA N RGD:5509061 20181227 MGI 735901 Nrxn2 neurexin II gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20240523 MGI 735901 Nrxn2 neurexin II gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:14983056 735901 Nrxn2 neurexin II gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:12827191 735901 Nrxn2 neurexin II gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:12827191 735901 Nrxn2 neurexin II gene MP:0002082 postnatal lethality IEA N RGD:5509061 20111116 MGI 735901 Nrxn2 neurexin II gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12827191 735901 Nrxn2 neurexin II gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111215 MGI 735901 Nrxn2 neurexin II gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12827191 735901 Nrxn2 neurexin II gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:14983056 735901 Nrxn2 neurexin II gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20150507 MGI PMID:25423136 735901 Nrxn2 neurexin II gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12827191 735901 Nrxn2 neurexin II gene MP:0002915 abnormal synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:12827191 735901 Nrxn2 neurexin II gene MP:0002945 abnormal inhibitory postsynaptic currents IEA N RGD:5509061 20111116 MGI 735901 Nrxn2 neurexin II gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20150507 MGI PMID:25423136 735901 Nrxn2 neurexin II gene MP:0003960 increased lean body mass IEA N RGD:5509061 20210826 MGI 735901 Nrxn2 neurexin II gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:12827191 735901 Nrxn2 neurexin II gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:12827191 735901 Nrxn2 neurexin II gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:12827191 735901 Nrxn2 neurexin II gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:12827191 735901 Nrxn2 neurexin II gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20240523 MGI 735901 Nrxn2 neurexin II gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 735901 Nrxn2 neurexin II gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20240523 MGI 735901 Nrxn2 neurexin II gene MP:0011003 reduced AMPA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12827191 735901 Nrxn2 neurexin II gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12827191 735901 Nrxn2 neurexin II gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12827191 735901 Nrxn2 neurexin II gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141003 MGI PMID:12827191 735902 Acan aggrecan gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:1952601 735902 Acan aggrecan gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10594233 735902 Acan aggrecan gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:1952601 735902 Acan aggrecan gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:632744 735902 Acan aggrecan gene MP:0000130 abnormal trabecular bone morphology IEA N RGD:5509061 20111116 MGI 735902 Acan aggrecan gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:632744 735902 Acan aggrecan gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:9192671 735902 Acan aggrecan gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20111116 MGI 735902 Acan aggrecan gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:9192671 735902 Acan aggrecan gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:9192671 735902 Acan aggrecan gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:1757493 735902 Acan aggrecan gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:632744 735902 Acan aggrecan gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:10594233 735902 Acan aggrecan gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:632744 735902 Acan aggrecan gene MP:0000447 flattened snout IAGP N RGD:5509061 20171019 MGI PMID:632744 735902 Acan aggrecan gene MP:0000547 short limbs IEA N RGD:5509061 20111116 MGI 735902 Acan aggrecan gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:632744 735902 Acan aggrecan gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:632744 735902 Acan aggrecan gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:9192671 735902 Acan aggrecan gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:2682579 735902 Acan aggrecan gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:2682579 735902 Acan aggrecan gene MP:0001261 obese IAGP N RGD:5509061 20160929 MGI PMID:27534441 735902 Acan aggrecan gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:10594233 735902 Acan aggrecan gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:632744 735902 Acan aggrecan gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9192671 735902 Acan aggrecan gene MP:0001438 aphagia IAGP N RGD:5509061 20141003 MGI PMID:9192671 735902 Acan aggrecan gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20201022 MGI 735902 Acan aggrecan gene MP:0001625 cardiac hypertrophy IEA N RGD:5509061 20141003 MGI 735902 Acan aggrecan gene MP:0001953 respiratory failure IEA N RGD:5509061 20111116 MGI 735902 Acan aggrecan gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:632744 735902 Acan aggrecan gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:1952601 735902 Acan aggrecan gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9192671 735902 Acan aggrecan gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20111116 MGI 735902 Acan aggrecan gene MP:0002116 abnormal craniofacial bone morphology IEA N RGD:5509061 20111116 MGI 735902 Acan aggrecan gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15798221 735902 Acan aggrecan gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19830818 735902 Acan aggrecan gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:1952601 735902 Acan aggrecan gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:9192671 735902 Acan aggrecan gene MP:0002544 brachydactyly IEA N RGD:5509061 20111116 MGI 735902 Acan aggrecan gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 735902 Acan aggrecan gene MP:0002772 brachypodia IEA N RGD:5509061 20141003 MGI 735902 Acan aggrecan gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20160929 MGI PMID:27534441 735902 Acan aggrecan gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:632744 735902 Acan aggrecan gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:33905568 735902 Acan aggrecan gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:632744 735902 Acan aggrecan gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:17510707 735902 Acan aggrecan gene MP:0004020 polyhydramnios IAGP N RGD:5509061 20141003 MGI PMID:2682579 735902 Acan aggrecan gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:9192671 735902 Acan aggrecan gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:632744 735902 Acan aggrecan gene MP:0004393 abnormal cochlear inner hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:1952601 735902 Acan aggrecan gene MP:0004403 absent cochlear outer hair cells IAGP N RGD:5509061 20141003 MGI PMID:1952601 735902 Acan aggrecan gene MP:0004653 absent caudal vertebrae IEA N RGD:5509061 20111116 MGI 735902 Acan aggrecan gene MP:0004684 intervertebral disk degeneration IAGP N RGD:5509061 20141003 MGI PMID:9192671 735902 Acan aggrecan gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:632744 735902 Acan aggrecan gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:632744 735902 Acan aggrecan gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:2682579 735902 Acan aggrecan gene MP:0004746 abnormal cochlear IHC afferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:1952601 735902 Acan aggrecan gene MP:0005330 cardiomyopathy IEA N RGD:5509061 20141003 MGI 735902 Acan aggrecan gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:10594233 735902 Acan aggrecan gene MP:0009908 protruding tongue IAGP N RGD:5509061 20141003 MGI PMID:10594233 735902 Acan aggrecan gene MP:0009908 protruding tongue IAGP N RGD:5509061 20141003 MGI PMID:632744 735902 Acan aggrecan gene MP:0010079 increased osteochondroma incidence IAGP N RGD:5509061 20171228 MGI PMID:28445472 735902 Acan aggrecan gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:1952601 735902 Acan aggrecan gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:632744 735902 Acan aggrecan gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735902 Acan aggrecan gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:1952601 735902 Acan aggrecan gene MP:0030420 short basicranium IEA N RGD:5509061 20171214 MGI 735905 Plec plectin gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18490514 735905 Plec plectin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18490514 735905 Plec plectin gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9389647 735905 Plec plectin gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16344482 735905 Plec plectin gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:9389647 735905 Plec plectin gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:9389647 735905 Plec plectin gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:17606998 735905 Plec plectin gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:17606998 735905 Plec plectin gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:9389647 735905 Plec plectin gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:17606998 735905 Plec plectin gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:22144912 735905 Plec plectin gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:9389647 735905 Plec plectin gene MP:0001232 absent epidermis stratum basale IAGP N RGD:5509061 20141003 MGI PMID:9389647 735905 Plec plectin gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9389647 735905 Plec plectin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9389647 735905 Plec plectin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17606998 735905 Plec plectin gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:17606998 735905 Plec plectin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17606998 735905 Plec plectin gene MP:0001785 edema IEA N RGD:5509061 20221215 MGI 735905 Plec plectin gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:16344482 735905 Plec plectin gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9389647 735905 Plec plectin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17606998 735905 Plec plectin gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16344482 735905 Plec plectin gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22144912 735905 Plec plectin gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9389647 735905 Plec plectin gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:17606998 735905 Plec plectin gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18490514 735905 Plec plectin gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18490514 735905 Plec plectin gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9389647 735905 Plec plectin gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22144912 735905 Plec plectin gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:16344482 735905 Plec plectin gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:18490514 735905 Plec plectin gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:18490514 735905 Plec plectin gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:16344482 735905 Plec plectin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19625254 735905 Plec plectin gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:9389647 735905 Plec plectin gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:18490514 735905 Plec plectin gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:19625254 735905 Plec plectin gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:18490514 735905 Plec plectin gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:18490514 735905 Plec plectin gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:18490514 735905 Plec plectin gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:18490514 735905 Plec plectin gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:18490514 735905 Plec plectin gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:18490514 735905 Plec plectin gene MP:0009473 abnormal skin exfoliation IAGP N RGD:5509061 20141003 MGI PMID:22144912 735905 Plec plectin gene MP:0009827 skin detachment IAGP N RGD:5509061 20170309 MGI PMID:9389647 735905 Plec plectin gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:18490514 735905 Plec plectin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17606998 735905 Plec plectin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9389647 735905 Plec plectin gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12904583 735905 Plec plectin gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210826 MGI 735905 Plec plectin gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20141003 MGI PMID:22144912 735905 Plec plectin gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:16344482 735905 Plec plectin gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:18490514 735905 Plec plectin gene MP:0014342 abnormal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:18490514 735905 Plec plectin gene MP:0020416 decreased fibroblast chemotaxis IAGP N RGD:5509061 20170223 MGI PMID:16344482 735906 Cav3 caveolin 3 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20230601 MGI 735906 Cav3 caveolin 3 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12057923 735906 Cav3 caveolin 3 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12138167 735906 Cav3 caveolin 3 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20180215 MGI PMID:19535499 735906 Cav3 caveolin 3 gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:11115849 735906 Cav3 caveolin 3 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:11259414 735906 Cav3 caveolin 3 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:11259414 735906 Cav3 caveolin 3 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20230601 MGI 735906 Cav3 caveolin 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12057923 735906 Cav3 caveolin 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12138167 735906 Cav3 caveolin 3 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:12057923 735906 Cav3 caveolin 3 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 735906 Cav3 caveolin 3 gene MP:0002280 abnormal intercostal muscle morphology IAGP N RGD:5509061 20180215 MGI PMID:19535499 735906 Cav3 caveolin 3 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12057923 735906 Cav3 caveolin 3 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12138167 735906 Cav3 caveolin 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:12057923 735906 Cav3 caveolin 3 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:12138167 735906 Cav3 caveolin 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12057923 735906 Cav3 caveolin 3 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20180215 MGI PMID:19535499 735906 Cav3 caveolin 3 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11259414 735906 Cav3 caveolin 3 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20180215 MGI PMID:19535499 735906 Cav3 caveolin 3 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12138167 735906 Cav3 caveolin 3 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20180215 MGI PMID:19535499 735906 Cav3 caveolin 3 gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:11259414 735906 Cav3 caveolin 3 gene MP:0004150 absent caveolae IAGP N RGD:5509061 20141003 MGI PMID:12057923 735906 Cav3 caveolin 3 gene MP:0004150 absent caveolae IAGP N RGD:5509061 20141003 MGI PMID:12138167 735906 Cav3 caveolin 3 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:12057923 735906 Cav3 caveolin 3 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:12138167 735906 Cav3 caveolin 3 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12138167 735906 Cav3 caveolin 3 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12057923 735906 Cav3 caveolin 3 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20230601 MGI 735906 Cav3 caveolin 3 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:11259414 735906 Cav3 caveolin 3 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20180215 MGI PMID:19535499 735906 Cav3 caveolin 3 gene MP:0009414 skeletal muscle fiber necrosis IAGP N RGD:5509061 20141003 MGI PMID:11259414 735906 Cav3 caveolin 3 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:11259414 735906 Cav3 caveolin 3 gene MP:0010581 abnormal atrium myocardial trabeculae morphology IAGP N RGD:5509061 20180215 MGI PMID:19535499 735906 Cav3 caveolin 3 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:12057923 735906 Cav3 caveolin 3 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:12138167 735906 Cav3 caveolin 3 gene MP:0011877 absent liver IEA N RGD:5509061 20230601 MGI 735906 Cav3 caveolin 3 gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:12057923 735906 Cav3 caveolin 3 gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:12138167 735906 Cav3 caveolin 3 gene MP:0021159 increased heart right ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:12057923 735906 Cav3 caveolin 3 gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:12057923 735906 Cav3 caveolin 3 gene MP:0031131 myocardial fiber disarray IAGP N RGD:5509061 20201015 MGI PMID:19535499 735906 Cav3 caveolin 3 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:12057923 735908 Chrna2 cholinergic receptor nicotinic alpha 2 subunit gene MP:0001200 thick skin IEA N RGD:5509061 20230601 MGI 735908 Chrna2 cholinergic receptor nicotinic alpha 2 subunit gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 735908 Chrna2 cholinergic receptor nicotinic alpha 2 subunit gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 735908 Chrna2 cholinergic receptor nicotinic alpha 2 subunit gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 735908 Chrna2 cholinergic receptor nicotinic alpha 2 subunit gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17466021 735908 Chrna2 cholinergic receptor nicotinic alpha 2 subunit gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20240502 MGI PMID:28507032 735908 Chrna2 cholinergic receptor nicotinic alpha 2 subunit gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20230601 MGI 735908 Chrna2 cholinergic receptor nicotinic alpha 2 subunit gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17466021 735908 Chrna2 cholinergic receptor nicotinic alpha 2 subunit gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17466021 735908 Chrna2 cholinergic receptor nicotinic alpha 2 subunit gene MP:0002989 small kidney IEA N RGD:5509061 20230601 MGI 735908 Chrna2 cholinergic receptor nicotinic alpha 2 subunit gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20240502 MGI PMID:28507032 735908 Chrna2 cholinergic receptor nicotinic alpha 2 subunit gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17466021 735908 Chrna2 cholinergic receptor nicotinic alpha 2 subunit gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20240502 MGI PMID:28507032 735908 Chrna2 cholinergic receptor nicotinic alpha 2 subunit gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20240502 MGI PMID:28507032 735916 Mtmr9 myotubularin related protein 9 gene MP:0000745 tremors IAGP N RGD:5509061 20230622 MGI PMID:22056831 735916 Mtmr9 myotubularin related protein 9 gene MP:0001265 decreased body size IAGP N RGD:5509061 20230622 MGI PMID:22056831 735916 Mtmr9 myotubularin related protein 9 gene MP:0001393 ataxia IAGP N RGD:5509061 20230622 MGI PMID:22056831 735916 Mtmr9 myotubularin related protein 9 gene MP:0002064 seizures IAGP N RGD:5509061 20230622 MGI PMID:22056831 735916 Mtmr9 myotubularin related protein 9 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20230622 MGI PMID:22056831 735916 Mtmr9 myotubularin related protein 9 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20230622 MGI PMID:22056831 735918 Mmp16 matrix metallopeptidase 16 gene MP:0000098 abnormal vomer bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 735918 Mmp16 matrix metallopeptidase 16 gene MP:0001399 hyperactivity IEA N RGD:5509061 20160421 MGI 735918 Mmp16 matrix metallopeptidase 16 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200402 MGI 735918 Mmp16 matrix metallopeptidase 16 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 735918 Mmp16 matrix metallopeptidase 16 gene MP:0003043 hypoalgesia IEA N RGD:5509061 20220519 MGI 735918 Mmp16 matrix metallopeptidase 16 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0004420 parietal bone hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0004455 pterygoid bone hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0009900 vomer bone hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0010870 absent bone trabeculae IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20170907 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0020955 increased mechanical nociceptive threshold IEA N RGD:5509061 20220519 MGI 735918 Mmp16 matrix metallopeptidase 16 gene MP:0030095 abnormal midface morphology IAGP N RGD:5509061 20170928 MGI PMID:18022611 735918 Mmp16 matrix metallopeptidase 16 gene MP:0030279 thin neurocranium IAGP N RGD:5509061 20171102 MGI PMID:18022611 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:20386739 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16055059 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17442505 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:17442505 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:11918288 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20150312 MGI PMID:22470123 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20150312 MGI PMID:22470123 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:16257225 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:8033209 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:8844056 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18093519 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19016890 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:21215802 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20151224 MGI PMID:25153086 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:21364941 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:21220020 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:21364941 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160128 MGI PMID:26306459 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:19016890 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20160616 MGI PMID:25432536 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19016890 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20160128 MGI PMID:26306459 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19016890 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20011099 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21220020 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21215802 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160128 MGI PMID:26306459 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160616 MGI PMID:25432536 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20171214 MGI PMID:28218824 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20171214 MGI PMID:28218824 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15876460 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19016890 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:20011099 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20160128 MGI PMID:26306459 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20160616 MGI PMID:25432536 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:19016890 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:20011099 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:21364941 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:8033209 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:21364941 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:21215802 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11008180 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:8033209 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:8844056 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20160128 MGI PMID:26306459 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20160128 MGI PMID:26306459 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16093389 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20210617 MGI PMID:33692361 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001486 abnormal startle reflex IAGP N RGD:5509061 20141003 MGI PMID:14981523 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:16055059 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:11301211 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:16887106 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:20011099 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:21364941 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20160616 MGI PMID:25432536 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:11301211 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:18093519 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:20011099 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:21364941 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:16055059 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:20011099 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20210617 MGI PMID:33692361 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:20011099 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20160616 MGI PMID:25432536 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20150312 MGI PMID:22470123 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:16093389 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:14981523 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:15876460 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:21220020 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20160128 MGI PMID:26306459 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:19103683 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:21215802 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20150312 MGI PMID:22470123 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11918288 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0002807 abnormal eye blink conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16055059 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19103683 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:21364941 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:21364941 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20160128 MGI PMID:26306459 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20210617 MGI PMID:33692361 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:18093519 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:17442505 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:21215802 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:11918288 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:18093519 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:21220020 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0004191 neuronal intranuclear inclusions IAGP N RGD:5509061 20141003 MGI PMID:12700164 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:19103683 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20210617 MGI PMID:33692361 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0004833 ovary atrophy IAGP N RGD:5509061 20150312 MGI PMID:22470123 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11008180 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18093519 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:20011099 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21215802 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21220020 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:8033209 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:8844056 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:15876460 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:20386739 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20150312 MGI PMID:22470123 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0006361 abnormal female germ cell morphology IAGP N RGD:5509061 20150312 MGI PMID:22470123 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18093519 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:21220020 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20151224 MGI PMID:25153086 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20150312 MGI PMID:22470123 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0008871 abnormal ovarian follicle number IAGP N RGD:5509061 20150312 MGI PMID:22470123 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:11301211 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:14981523 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:21364941 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20160616 MGI PMID:25432536 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20150312 MGI PMID:22470123 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0009372 abnormal cumulus oophorus morphology IAGP N RGD:5509061 20150312 MGI PMID:22470123 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16093389 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:21215802 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:21220020 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:9144249 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20160616 MGI PMID:25432536 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:20386739 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19103683 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:15876460 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0011737 hypodipsia IAGP N RGD:5509061 20171214 MGI PMID:28218824 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20151224 MGI PMID:25153086 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20151224 MGI PMID:25153086 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0014373 increased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:33692361 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20210617 MGI PMID:33692361 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20210617 MGI PMID:33692361 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0020395 abnormal response to social novelty IAGP N RGD:5509061 20210617 MGI PMID:33692361 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171214 MGI PMID:28218824 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0020507 increased dendritic spine density IAGP N RGD:5509061 20210617 MGI PMID:33692361 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20210617 MGI PMID:33692361 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20240627 MGI PMID:21364941 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:22470123 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:20011099 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:21220020 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:26306459 735920 Fmr1 fragile X messenger ribonucleoprotein 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:8033209 735922 Il5ra interleukin 5 receptor, alpha gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15219462 735922 Il5ra interleukin 5 receptor, alpha gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15219462 735922 Il5ra interleukin 5 receptor, alpha gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22174445 735922 Il5ra interleukin 5 receptor, alpha gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:8630733 735922 Il5ra interleukin 5 receptor, alpha gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15128785 735922 Il5ra interleukin 5 receptor, alpha gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:8630733 735922 Il5ra interleukin 5 receptor, alpha gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15128785 735922 Il5ra interleukin 5 receptor, alpha gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:8630733 735922 Il5ra interleukin 5 receptor, alpha gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8630733 735922 Il5ra interleukin 5 receptor, alpha gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8630733 735922 Il5ra interleukin 5 receptor, alpha gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:15219462 735922 Il5ra interleukin 5 receptor, alpha gene MP:0002360 abnormal spleen B cell corona morphology IAGP N RGD:5509061 20141003 MGI PMID:15219462 735922 Il5ra interleukin 5 receptor, alpha gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8630733 735922 Il5ra interleukin 5 receptor, alpha gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:8630733 735922 Il5ra interleukin 5 receptor, alpha gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15219462 735922 Il5ra interleukin 5 receptor, alpha gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:15219462 735922 Il5ra interleukin 5 receptor, alpha gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:15219462 735922 Il5ra interleukin 5 receptor, alpha gene MP:0002602 abnormal eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:8630733 735922 Il5ra interleukin 5 receptor, alpha gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:15219462 735922 Il5ra interleukin 5 receptor, alpha gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:15219462 735922 Il5ra interleukin 5 receptor, alpha gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:15219462 735922 Il5ra interleukin 5 receptor, alpha gene MP:0004940 abnormal B-1 B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15128785 735922 Il5ra interleukin 5 receptor, alpha gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:15128785 735922 Il5ra interleukin 5 receptor, alpha gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:15219462 735922 Il5ra interleukin 5 receptor, alpha gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:8630733 735922 Il5ra interleukin 5 receptor, alpha gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15128785 735922 Il5ra interleukin 5 receptor, alpha gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:8630733 735922 Il5ra interleukin 5 receptor, alpha gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:15128785 735922 Il5ra interleukin 5 receptor, alpha gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:15128785 735922 Il5ra interleukin 5 receptor, alpha gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:8630733 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:14975714 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0000276 heart right ventricle hypertrophy IAGP N RGD:5509061 20240125 MGI PMID:14975714 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14975714 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0000293 absent myocardial trabeculae IAGP N RGD:5509061 20141003 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:14975714 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0000301 decreased atrioventricular cushion size IAGP N RGD:5509061 20141003 MGI PMID:14975714 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:14975714 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:14975714 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:14975714 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:14975714 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0006117 aortic valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:14975714 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0010423 heart right ventricle aneurysm IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0010455 aortopulmonary window IAGP N RGD:5509061 20141003 MGI PMID:14975714 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0010563 increased heart right ventricle size IAGP N RGD:5509061 20240125 MGI PMID:14975714 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0010594 thick aortic valve IAGP N RGD:5509061 20141003 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0010605 thick pulmonary valve cusps IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0010618 enlarged mitral valve IAGP N RGD:5509061 20141003 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0010620 thick mitral valve IAGP N RGD:5509061 20141003 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0010629 thick tricuspid valve IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0010629 thick tricuspid valve IAGP N RGD:5509061 20141003 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14673146 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14975714 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0031554 abnormal aortic valve development IAGP N RGD:5509061 20240125 MGI PMID:14975714 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0031555 abnormal pulmonary valve development IAGP N RGD:5509061 20240125 MGI PMID:14975714 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0031558 tricuspid valve hyperplasia IAGP N RGD:5509061 20240104 MGI PMID:15936750 735924 Adam19 ADAM metallopeptidase domain 19 gene MP:0031581 semilunar valve hyperplasia IAGP N RGD:5509061 20240125 MGI PMID:15936750 735926 Fxyd6 FXYD domain-containing ion transport regulator 6 gene MP:0009456 impaired cued conditioning behavior IEA N RGD:5509061 20141003 MGI 735930 Pias2 protein inhibitor of activated STAT 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20151112 MGI PMID:15956336 735930 Pias2 protein inhibitor of activated STAT 2 gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20151112 MGI PMID:15956336 735930 Pias2 protein inhibitor of activated STAT 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 735930 Pias2 protein inhibitor of activated STAT 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201231 MGI 735930 Pias2 protein inhibitor of activated STAT 2 gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 735930 Pias2 protein inhibitor of activated STAT 2 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20150430 MGI 735930 Pias2 protein inhibitor of activated STAT 2 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20151112 MGI PMID:15956336 735930 Pias2 protein inhibitor of activated STAT 2 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20151112 MGI PMID:15956336 735930 Pias2 protein inhibitor of activated STAT 2 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20150108 MGI 735930 Pias2 protein inhibitor of activated STAT 2 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 735930 Pias2 protein inhibitor of activated STAT 2 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20151112 MGI PMID:15956336 735930 Pias2 protein inhibitor of activated STAT 2 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20151112 MGI PMID:15956336 735930 Pias2 protein inhibitor of activated STAT 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20151112 MGI PMID:15956336 735930 Pias2 protein inhibitor of activated STAT 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 735930 Pias2 protein inhibitor of activated STAT 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 735937 Plcg1 phospholipase C, gamma 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11744703 735937 Plcg1 phospholipase C, gamma 1 gene MP:0001721 absent visceral yolk sac blood islands IAGP N RGD:5509061 20141003 MGI PMID:11744703 735937 Plcg1 phospholipase C, gamma 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9096335 735937 Plcg1 phospholipase C, gamma 1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0001849 ear inflammation IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20141003 MGI PMID:11744703 735937 Plcg1 phospholipase C, gamma 1 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11744703 735937 Plcg1 phospholipase C, gamma 1 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11748152 735937 Plcg1 phospholipase C, gamma 1 gene MP:0003542 abnormal vascular endothelial cell development IAGP N RGD:5509061 20141003 MGI PMID:11744703 735937 Plcg1 phospholipase C, gamma 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9096335 735937 Plcg1 phospholipase C, gamma 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:20123962 735937 Plcg1 phospholipase C, gamma 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9096335 735937 Plcg1 phospholipase C, gamma 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11744703 735937 Plcg1 phospholipase C, gamma 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11748152 735937 Plcg1 phospholipase C, gamma 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9096335 735939 Anxa4 annexin A4 gene MP:0001386 abnormal maternal nurturing IAGP N RGD:5509061 20141003 MGI PMID:12912993 735942 Crem cAMP responsive element modulator gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:17376811 735942 Crem cAMP responsive element modulator gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:8600391 735942 Crem cAMP responsive element modulator gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:8600390 735942 Crem cAMP responsive element modulator gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:14757819 735942 Crem cAMP responsive element modulator gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:8600390 735942 Crem cAMP responsive element modulator gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:21408140 735942 Crem cAMP responsive element modulator gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18562617 735942 Crem cAMP responsive element modulator gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10570204 735942 Crem cAMP responsive element modulator gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:10570204 735942 Crem cAMP responsive element modulator gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18562617 735942 Crem cAMP responsive element modulator gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18562617 735942 Crem cAMP responsive element modulator gene MP:0001499 abnormal kindling response IAGP N RGD:5509061 20141003 MGI PMID:18562617 735942 Crem cAMP responsive element modulator gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:8600391 735942 Crem cAMP responsive element modulator gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14757819 735942 Crem cAMP responsive element modulator gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8600390 735942 Crem cAMP responsive element modulator gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:8600391 735942 Crem cAMP responsive element modulator gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8600391 735942 Crem cAMP responsive element modulator gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17376811 735942 Crem cAMP responsive element modulator gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:8600390 735942 Crem cAMP responsive element modulator gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:9851970 735942 Crem cAMP responsive element modulator gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:8600391 735942 Crem cAMP responsive element modulator gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:8600391 735942 Crem cAMP responsive element modulator gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:10570204 735942 Crem cAMP responsive element modulator gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:9851970 735942 Crem cAMP responsive element modulator gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:12475904 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:20855892 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21896769 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21896769 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22586267 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20855892 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20855892 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22586267 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20855892 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0002715 decreased glycogen catabolism rate IAGP N RGD:5509061 20141003 MGI PMID:22586267 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20141003 MGI PMID:21896769 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22586267 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:20855892 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22586267 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21896769 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22586267 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:21896769 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:20855892 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20855892 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20181227 MGI 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:20855892 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22586267 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:20855892 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:20855892 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:22586267 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21896769 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:20855892 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:21896769 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:22586267 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:20855892 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0030022 decreased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:21896769 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0030022 decreased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:22586267 735944 Prkab2 protein kinase, AMP-activated, beta 2 non-catalytic subunit gene MP:0031618 decreased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:20855892 735946 Rack1 receptor for activated C kinase 1 gene MP:0000373 belly spot IAGP N RGD:5509061 20200310 MGI PMID:23212600 735946 Rack1 receptor for activated C kinase 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20200310 MGI PMID:23212600 735946 Rack1 receptor for activated C kinase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200310 MGI PMID:23212600 735946 Rack1 receptor for activated C kinase 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20200310 MGI PMID:23212600 735946 Rack1 receptor for activated C kinase 1 gene MP:0001694 absent egg cylinders IAGP N RGD:5509061 20200310 MGI PMID:23212600 735946 Rack1 receptor for activated C kinase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20200310 MGI PMID:23212600 735946 Rack1 receptor for activated C kinase 1 gene MP:0005175 non-pigmented tail tip IAGP N RGD:5509061 20200310 MGI PMID:23212600 735946 Rack1 receptor for activated C kinase 1 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:23212600 735946 Rack1 receptor for activated C kinase 1 gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20200310 MGI PMID:23212600 735946 Rack1 receptor for activated C kinase 1 gene MP:0011568 decreased foot pigmentation IAGP N RGD:5509061 20200310 MGI PMID:23212600 735946 Rack1 receptor for activated C kinase 1 gene MP:0013272 abnormal translation IAGP N RGD:5509061 20200310 MGI PMID:23212600 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20181227 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20181227 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210128 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0000495 abnormal colon morphology IEA N RGD:5509061 20181227 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20170427 MGI PMID:17207605 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0000623 decreased salivation IAGP N RGD:5509061 20170427 MGI PMID:17207605 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12391195 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19528538 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12391195 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20211021 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0001469 abnormal contextual conditioning behavior IEA N RGD:5509061 20211021 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20181227 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12391195 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0001657 abnormal induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12391195 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:12391195 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:19528538 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0001861 lung inflammation IAGP N RGD:5509061 20170427 MGI PMID:17207605 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20170427 MGI PMID:17207605 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0002221 abnormal lymph organ size IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20211021 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0002834 decreased heart weight IEA N RGD:5509061 20181227 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210128 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20210128 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0003271 abnormal duodenum morphology IEA N RGD:5509061 20181227 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20170427 MGI PMID:17207605 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0003896 prolonged PR interval IEA N RGD:5509061 20211021 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12391195 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16227983 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20191031 MGI PMID:30560927 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16227983 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:16227983 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20211021 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20181227 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20181227 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20210128 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20210128 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0008049 increased memory T cell number IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21508411 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0008500 increased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:7584142 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20170427 MGI PMID:17207605 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0009517 abnormal salivary gland duct morphology IAGP N RGD:5509061 20170427 MGI PMID:17207605 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20211021 MGI 735948 Il2ra interleukin 2 receptor, alpha chain gene MP:0020420 abnormal freezing behavior IEA N RGD:5509061 20210128 MGI 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18669642 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0000282 abnormal interatrial septum morphology IAGP N RGD:5509061 20141003 MGI PMID:20185768 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0000288 abnormal pericardium morphology IAGP N RGD:5509061 20141003 MGI PMID:20185768 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20185768 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:21515572 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:18669642 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:18669642 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20185768 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:18669642 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18669642 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20185768 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:20185768 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:18669642 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20185768 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:20185768 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:20185768 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0004096 abnormal midbrain-hindbrain boundary development IAGP N RGD:5509061 20141003 MGI PMID:18669642 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:20185768 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:21515572 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:20185768 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:18669642 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:20185768 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0010656 thick myocardium IAGP N RGD:5509061 20141003 MGI PMID:20185768 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18669642 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20185768 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:18669642 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0012090 midbrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18669642 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0012263 decreased hindbrain size IAGP N RGD:5509061 20141003 MGI PMID:18669642 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0012264 hindbrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18669642 735954 Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20185768 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18450958 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:18450958 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18450958 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:23236168 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:23236168 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0004184 abnormal baroreceptor physiology IAGP N RGD:5509061 20141003 MGI PMID:18450958 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18450958 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:18450958 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:23236168 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23236168 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:18450958 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20141003 MGI PMID:23236168 735956 Gpsm1 G-protein signalling modulator 1 (AGS3-like, C. elegans) gene MP:0012125 decreased bronchoconstrictive response IEA N RGD:5509061 20210128 MGI 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20181227 MGI 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15161873 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0001006 abnormal retina cone cell morphology IEA N RGD:5509061 20111116 MGI 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:10377453 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:15161873 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:17724338 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21052544 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20181227 MGI 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:10377453 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10377453 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11528395 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15161873 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15161873 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15161873 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15161873 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20161020 MGI PMID:22509403 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20230713 MGI PMID:12808468 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20161020 MGI PMID:22509403 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:10377453 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20161020 MGI PMID:22509403 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:15161873 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20161020 MGI PMID:22509403 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0009943 abnormal olfactory bulb periglomerular cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17724338 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0011831 abnormal visual contrast sensitivity IAGP N RGD:5509061 20161020 MGI PMID:22509403 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20161020 MGI PMID:22509403 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:12808468 735957 Cnga3 cyclic nucleotide gated channel alpha 3 gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:12808468 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:12808456 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:17522159 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:7517224 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0000520 absent kidney IAGP N RGD:5509061 20150507 MGI PMID:15198975 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12808456 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12808456 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20150507 MGI 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:12808456 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:12808456 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:21303853 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21303853 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:21303853 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17522159 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:12808456 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:12808456 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:7517224 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21303853 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0002187 abnormal fibula morphology IEA N RGD:5509061 20150507 MGI 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20150507 MGI PMID:15198975 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:21303853 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0003446 renal hypoplasia IEA N RGD:5509061 20111116 MGI 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:17522159 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:7517224 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0003722 absent ureter IAGP N RGD:5509061 20150507 MGI PMID:15198975 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0003723 abnormal long bone morphology IEA N RGD:5509061 20150507 MGI 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0004639 fused metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20150507 MGI PMID:2612902 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:19383632 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20141003 MGI PMID:21303853 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0006295 absent sclerotome IAGP N RGD:5509061 20141003 MGI PMID:21303853 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20160609 MGI PMID:17785465 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20160609 MGI PMID:17785465 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0010982 abnormal ureteric bud elongation IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0010982 abnormal ureteric bud elongation IAGP N RGD:5509061 20141003 MGI PMID:7517224 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0010984 abnormal metanephric mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:7517224 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12808456 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0011261 abnormal limb mesenchyme morphology IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0011366 absent metanephros IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0011386 increased metanephric mesenchyme apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0011504 abnormal limb long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15201225 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0011530 fused radius and ulna IEA N RGD:5509061 20150507 MGI 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20160609 MGI PMID:17785465 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:21303853 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0012176 abnormal head development IAGP N RGD:5509061 20141003 MGI PMID:21303853 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20160609 MGI PMID:17785465 735959 Grem1 gremlin 1, DAN family BMP antagonist gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20160609 MGI PMID:17785465 735963 Slco1a4 solute carrier organic anion transporter family, member 1a4 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21561886 735963 Slco1a4 solute carrier organic anion transporter family, member 1a4 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21561886 735963 Slco1a4 solute carrier organic anion transporter family, member 1a4 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21561886 735965 Decr2 2-4-dienoyl-Coenzyme A reductase 2, peroxisomal gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20211021 MGI 735965 Decr2 2-4-dienoyl-Coenzyme A reductase 2, peroxisomal gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20210520 MGI 735965 Decr2 2-4-dienoyl-Coenzyme A reductase 2, peroxisomal gene MP:0005573 increased pulmonary respiratory rate IEA N RGD:5509061 20211021 MGI 735965 Decr2 2-4-dienoyl-Coenzyme A reductase 2, peroxisomal gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 735967 Ppp1r14c protein phosphatase 1, regulatory inhibitor subunit 14C gene MP:0001981 increased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:19819304 735967 Ppp1r14c protein phosphatase 1, regulatory inhibitor subunit 14C gene MP:0009711 abnormal conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:19819304 735967 Ppp1r14c protein phosphatase 1, regulatory inhibitor subunit 14C gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:19819304 735967 Ppp1r14c protein phosphatase 1, regulatory inhibitor subunit 14C gene MP:0009753 enhanced behavioral response to morphine IAGP N RGD:5509061 20141003 MGI PMID:19819304 735967 Ppp1r14c protein phosphatase 1, regulatory inhibitor subunit 14C gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19819304 735967 Ppp1r14c protein phosphatase 1, regulatory inhibitor subunit 14C gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200625 MGI PMID:27663205 735968 Mapk12 mitogen-activated protein kinase 12 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15729360 735968 Mapk12 mitogen-activated protein kinase 12 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19936205 735968 Mapk12 mitogen-activated protein kinase 12 gene MP:0006039 decreased mitochondrial fission IAGP N RGD:5509061 20141003 MGI PMID:19936205 735969 Smo smoothened, frizzled class receptor gene MP:0000040 absent middle ear ossicles IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0000099 absent vomer bone IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0000100 abnormal ethmoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20171005 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0000265 blood vessel atresia IAGP N RGD:5509061 20141003 MGI PMID:23873040 735969 Smo smoothened, frizzled class receptor gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:9636176 735969 Smo smoothened, frizzled class receptor gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20160811 MGI 735969 Smo smoothened, frizzled class receptor gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:12372301 735969 Smo smoothened, frizzled class receptor gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23332756 735969 Smo smoothened, frizzled class receptor gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:23645682 735969 Smo smoothened, frizzled class receptor gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:11748145 735969 Smo smoothened, frizzled class receptor gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:16571625 735969 Smo smoothened, frizzled class receptor gene MP:0000784 forebrain hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19854269 735969 Smo smoothened, frizzled class receptor gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20210114 MGI PMID:32702291 735969 Smo smoothened, frizzled class receptor gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:19854269 735969 Smo smoothened, frizzled class receptor gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:19357274 735969 Smo smoothened, frizzled class receptor gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:18480159 735969 Smo smoothened, frizzled class receptor gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:16571625 735969 Smo smoothened, frizzled class receptor gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:18480159 735969 Smo smoothened, frizzled class receptor gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:16571625 735969 Smo smoothened, frizzled class receptor gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:18480159 735969 Smo smoothened, frizzled class receptor gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:16571625 735969 Smo smoothened, frizzled class receptor gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:18480159 735969 Smo smoothened, frizzled class receptor gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:18480159 735969 Smo smoothened, frizzled class receptor gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19549984 735969 Smo smoothened, frizzled class receptor gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22698544 735969 Smo smoothened, frizzled class receptor gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22698544 735969 Smo smoothened, frizzled class receptor gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16061793 735969 Smo smoothened, frizzled class receptor gene MP:0000933 abnormal rhombomere morphology IAGP N RGD:5509061 20141003 MGI PMID:18480159 735969 Smo smoothened, frizzled class receptor gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:16061793 735969 Smo smoothened, frizzled class receptor gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:15755804 735969 Smo smoothened, frizzled class receptor gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23645682 735969 Smo smoothened, frizzled class receptor gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:19854269 735969 Smo smoothened, frizzled class receptor gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17881493 735969 Smo smoothened, frizzled class receptor gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:24302887 735969 Smo smoothened, frizzled class receptor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12372301 735969 Smo smoothened, frizzled class receptor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:19854269 735969 Smo smoothened, frizzled class receptor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9636176 735969 Smo smoothened, frizzled class receptor gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12372301 735969 Smo smoothened, frizzled class receptor gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17881493 735969 Smo smoothened, frizzled class receptor gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9636176 735969 Smo smoothened, frizzled class receptor gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15755804 735969 Smo smoothened, frizzled class receptor gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20160616 MGI PMID:25760946 735969 Smo smoothened, frizzled class receptor gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:17881493 735969 Smo smoothened, frizzled class receptor gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:19223390 735969 Smo smoothened, frizzled class receptor gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:9636176 735969 Smo smoothened, frizzled class receptor gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9636176 735969 Smo smoothened, frizzled class receptor gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20190502 MGI 735969 Smo smoothened, frizzled class receptor gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16687132 735969 Smo smoothened, frizzled class receptor gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12372301 735969 Smo smoothened, frizzled class receptor gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:11748145 735969 Smo smoothened, frizzled class receptor gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:11748145 735969 Smo smoothened, frizzled class receptor gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:23873040 735969 Smo smoothened, frizzled class receptor gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19223390 735969 Smo smoothened, frizzled class receptor gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19549984 735969 Smo smoothened, frizzled class receptor gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21209331 735969 Smo smoothened, frizzled class receptor gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23332756 735969 Smo smoothened, frizzled class receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16221724 735969 Smo smoothened, frizzled class receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16854976 735969 Smo smoothened, frizzled class receptor gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:17344228 735969 Smo smoothened, frizzled class receptor gene MP:0002260 abnormal thyroid cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16687132 735969 Smo smoothened, frizzled class receptor gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:17344228 735969 Smo smoothened, frizzled class receptor gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:23873040 735969 Smo smoothened, frizzled class receptor gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:12403705 735969 Smo smoothened, frizzled class receptor gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20141003 MGI PMID:12403705 735969 Smo smoothened, frizzled class receptor gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:11748145 735969 Smo smoothened, frizzled class receptor gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:11748145 735969 Smo smoothened, frizzled class receptor gene MP:0002809 increased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:19223390 735969 Smo smoothened, frizzled class receptor gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:17344228 735969 Smo smoothened, frizzled class receptor gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:17344228 735969 Smo smoothened, frizzled class receptor gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17881493 735969 Smo smoothened, frizzled class receptor gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:20943901 735969 Smo smoothened, frizzled class receptor gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:12372301 735969 Smo smoothened, frizzled class receptor gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:19854269 735969 Smo smoothened, frizzled class receptor gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23645682 735969 Smo smoothened, frizzled class receptor gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23873040 735969 Smo smoothened, frizzled class receptor gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20210128 MGI 735969 Smo smoothened, frizzled class receptor gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19549984 735969 Smo smoothened, frizzled class receptor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160616 MGI PMID:25760946 735969 Smo smoothened, frizzled class receptor gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:16687132 735969 Smo smoothened, frizzled class receptor gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:17344228 735969 Smo smoothened, frizzled class receptor gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:16687132 735969 Smo smoothened, frizzled class receptor gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:16687132 735969 Smo smoothened, frizzled class receptor gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9636176 735969 Smo smoothened, frizzled class receptor gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:16061793 735969 Smo smoothened, frizzled class receptor gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:19854269 735969 Smo smoothened, frizzled class receptor gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:19854269 735969 Smo smoothened, frizzled class receptor gene MP:0004318 absent incus IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0004319 absent malleus IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0004340 short scapula IAGP N RGD:5509061 20141003 MGI PMID:11748145 735969 Smo smoothened, frizzled class receptor gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:11748145 735969 Smo smoothened, frizzled class receptor gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:11748145 735969 Smo smoothened, frizzled class receptor gene MP:0004449 absent presphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0004454 absent pterygoid process IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0004459 small alisphenoid bone IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0004468 small zygomatic bone IAGP N RGD:5509061 20171005 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0004574 broad limb buds IAGP N RGD:5509061 20141003 MGI PMID:9636176 735969 Smo smoothened, frizzled class receptor gene MP:0004595 abnormal mandibular condyloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:11748145 735969 Smo smoothened, frizzled class receptor gene MP:0004791 absent lower incisors IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0004837 abnormal neural fold formation IAGP N RGD:5509061 20141003 MGI PMID:12372301 735969 Smo smoothened, frizzled class receptor gene MP:0004916 absent Reichert cartilage IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0004949 absent neuronal precursor cells IAGP N RGD:5509061 20141003 MGI PMID:19549984 735969 Smo smoothened, frizzled class receptor gene MP:0004979 abnormal neuronal precursor cell number IAGP N RGD:5509061 20180215 MGI PMID:28817564 735969 Smo smoothened, frizzled class receptor gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20160616 MGI PMID:25760946 735969 Smo smoothened, frizzled class receptor gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210128 MGI 735969 Smo smoothened, frizzled class receptor gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:12403705 735969 Smo smoothened, frizzled class receptor gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:19854269 735969 Smo smoothened, frizzled class receptor gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12372301 735969 Smo smoothened, frizzled class receptor gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:19854269 735969 Smo smoothened, frizzled class receptor gene MP:0006104 abnormal tectum morphology IAGP N RGD:5509061 20141003 MGI PMID:18480159 735969 Smo smoothened, frizzled class receptor gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:16687132 735969 Smo smoothened, frizzled class receptor gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:17344228 735969 Smo smoothened, frizzled class receptor gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:12372301 735969 Smo smoothened, frizzled class receptor gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16687132 735969 Smo smoothened, frizzled class receptor gene MP:0008381 absent gonial bone IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0008386 absent styloid process IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0008802 abnormal intestinal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23645682 735969 Smo smoothened, frizzled class receptor gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:23645682 735969 Smo smoothened, frizzled class receptor gene MP:0009048 enlarged tectum IAGP N RGD:5509061 20141003 MGI PMID:18480159 735969 Smo smoothened, frizzled class receptor gene MP:0009844 abnormal neural crest cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17344228 735969 Smo smoothened, frizzled class receptor gene MP:0009905 absent tongue IAGP N RGD:5509061 20141003 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:19549984 735969 Smo smoothened, frizzled class receptor gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:23645682 735969 Smo smoothened, frizzled class receptor gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20141003 MGI PMID:23645682 735969 Smo smoothened, frizzled class receptor gene MP:0010335 fused first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:12372301 735969 Smo smoothened, frizzled class receptor gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16687132 735969 Smo smoothened, frizzled class receptor gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:16687132 735969 Smo smoothened, frizzled class receptor gene MP:0010460 pulmonary artery hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17344228 735969 Smo smoothened, frizzled class receptor gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 735969 Smo smoothened, frizzled class receptor gene MP:0010747 abnormal enamel organ morphology IAGP N RGD:5509061 20171221 MGI PMID:12403705 735969 Smo smoothened, frizzled class receptor gene MP:0010802 abnormal intestinal enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23645682 735969 Smo smoothened, frizzled class receptor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11748145 735969 Smo smoothened, frizzled class receptor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16571625 735969 Smo smoothened, frizzled class receptor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12403705 735969 Smo smoothened, frizzled class receptor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23645682 735969 Smo smoothened, frizzled class receptor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20160616 MGI PMID:25760946 735969 Smo smoothened, frizzled class receptor gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20210114 MGI PMID:32702291 735969 Smo smoothened, frizzled class receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15755804 735969 Smo smoothened, frizzled class receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16061793 735969 Smo smoothened, frizzled class receptor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19666503 735969 Smo smoothened, frizzled class receptor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735969 Smo smoothened, frizzled class receptor gene MP:0011210 abnormal temporomandibular joint morphology IAGP N RGD:5509061 20141003 MGI PMID:19815519 735969 Smo smoothened, frizzled class receptor gene MP:0012139 increased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:16357211 735969 Smo smoothened, frizzled class receptor gene MP:0012749 decreased cardiac neural crest cell number IAGP N RGD:5509061 20141003 MGI PMID:17344228 735969 Smo smoothened, frizzled class receptor gene MP:0012751 impaired cardiac neural crest cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17344228 735969 Smo smoothened, frizzled class receptor gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:16687132 735969 Smo smoothened, frizzled class receptor gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 735969 Smo smoothened, frizzled class receptor gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:11748145 735969 Smo smoothened, frizzled class receptor gene MP:0030057 absent lacrimal bone IAGP N RGD:5509061 20170921 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0030102 absent orbitosphenoid bone IAGP N RGD:5509061 20170928 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0030121 small temporal bone squamous part IAGP N RGD:5509061 20171005 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0030198 nasal septum hypoplasia IAGP N RGD:5509061 20171012 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0030258 small mandibular condyloid process IAGP N RGD:5509061 20171019 MGI PMID:19815519 735969 Smo smoothened, frizzled class receptor gene MP:0030374 Meckel's cartilage hypoplasia IAGP N RGD:5509061 20171207 MGI PMID:15107405 735969 Smo smoothened, frizzled class receptor gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20171221 MGI PMID:12403705 735969 Smo smoothened, frizzled class receptor gene MP:0030473 fused molars IAGP N RGD:5509061 20171221 MGI PMID:12403705 735969 Smo smoothened, frizzled class receptor gene MP:0030514 absent Tomes' process IAGP N RGD:5509061 20180111 MGI PMID:12403705 735969 Smo smoothened, frizzled class receptor gene MP:0030518 abnormal outer dental epithelium morphology IAGP N RGD:5509061 20180118 MGI PMID:12403705 735969 Smo smoothened, frizzled class receptor gene MP:0030519 abnormal inner dental epithelium morphology IAGP N RGD:5509061 20180118 MGI PMID:12403705 735969 Smo smoothened, frizzled class receptor gene MP:0030522 abnormal stellate reticulum morphology IAGP N RGD:5509061 20180118 MGI PMID:12403705 735969 Smo smoothened, frizzled class receptor gene MP:0030527 absent enamel cord IAGP N RGD:5509061 20180118 MGI PMID:12403705 735969 Smo smoothened, frizzled class receptor gene MP:0031442 enlarged cerebral aqueduct IAGP N RGD:5509061 20221103 MGI PMID:18480159 735971 Tpsb2 tryptase beta 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:17456473 735971 Tpsb2 tryptase beta 2 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:19109198 735971 Tpsb2 tryptase beta 2 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:18354212 735971 Tpsb2 tryptase beta 2 gene MP:0005462 abnormal mast cell differentiation IAGP N RGD:5509061 20150416 MGI PMID:19109198 735971 Tpsb2 tryptase beta 2 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:19109198 735971 Tpsb2 tryptase beta 2 gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18354212 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0000743 muscle spasm IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11717424 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:11717424 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0003450 enlarged pancreas IAGP N RGD:5509061 20141003 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0003892 abnormal gastric gland morphology IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:11717424 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0009160 abnormal pancreatic acinar cell zymogen granule morphology IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0009978 abnormal cerebellum white matter morphology IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0010797 abnormal pyloric gastric gland morphology IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0011416 abnormal testis interstitial tissue morphology IAGP N RGD:5509061 20150226 MGI PMID:14528005 735972 Ppt2 palmitoyl-protein thioesterase 2 gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:14528005 735973 Psen1 presenilin 1 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:10421573 735973 Psen1 presenilin 1 gene MP:0000079 abnormal basioccipital bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20305648 735973 Psen1 presenilin 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0000140 absent vertebral pedicles IAGP N RGD:5509061 20141003 MGI PMID:10932180 735973 Psen1 presenilin 1 gene MP:0000140 absent vertebral pedicles IAGP N RGD:5509061 20141003 MGI PMID:11262239 735973 Psen1 presenilin 1 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:11262239 735973 Psen1 presenilin 1 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:11262239 735973 Psen1 presenilin 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:12834865 735973 Psen1 presenilin 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:12834865 735973 Psen1 presenilin 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:10557208 735973 Psen1 presenilin 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15254914 735973 Psen1 presenilin 1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:10518543 735973 Psen1 presenilin 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11738035 735973 Psen1 presenilin 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15525534 735973 Psen1 presenilin 1 gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:15525534 735973 Psen1 presenilin 1 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141003 MGI PMID:15525534 735973 Psen1 presenilin 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:12391611 735973 Psen1 presenilin 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:12834865 735973 Psen1 presenilin 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:21725313 735973 Psen1 presenilin 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:9450754 735973 Psen1 presenilin 1 gene MP:0000592 short tail IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:15148382 735973 Psen1 presenilin 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:10557208 735973 Psen1 presenilin 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10421573 735973 Psen1 presenilin 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15148382 735973 Psen1 presenilin 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:12391611 735973 Psen1 presenilin 1 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:10421573 735973 Psen1 presenilin 1 gene MP:0000798 abnormal frontal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:18974993 735973 Psen1 presenilin 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:18585693 735973 Psen1 presenilin 1 gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:11738035 735973 Psen1 presenilin 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:18585693 735973 Psen1 presenilin 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:18974993 735973 Psen1 presenilin 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:10518543 735973 Psen1 presenilin 1 gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:22459153 735973 Psen1 presenilin 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:15525534 735973 Psen1 presenilin 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:15525534 735973 Psen1 presenilin 1 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:15525534 735973 Psen1 presenilin 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15525534 735973 Psen1 presenilin 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16963164 735973 Psen1 presenilin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15148382 735973 Psen1 presenilin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15525534 735973 Psen1 presenilin 1 gene MP:0001313 increased incidence of corneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22336193 735973 Psen1 presenilin 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:24278307 735973 Psen1 presenilin 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15148382 735973 Psen1 presenilin 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:24278307 735973 Psen1 presenilin 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16963164 735973 Psen1 presenilin 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:11978821 735973 Psen1 presenilin 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:15148382 735973 Psen1 presenilin 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11567612 735973 Psen1 presenilin 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15908021 735973 Psen1 presenilin 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:11738035 735973 Psen1 presenilin 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15207348 735973 Psen1 presenilin 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15748844 735973 Psen1 presenilin 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0001488 increased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:15908021 735973 Psen1 presenilin 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 735973 Psen1 presenilin 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16963164 735973 Psen1 presenilin 1 gene MP:0001575 cyanosis IEA N RGD:5509061 20210520 MGI 735973 Psen1 presenilin 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12834865 735973 Psen1 presenilin 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15081359 735973 Psen1 presenilin 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15148382 735973 Psen1 presenilin 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:10557208 735973 Psen1 presenilin 1 gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:10557208 735973 Psen1 presenilin 1 gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12391611 735973 Psen1 presenilin 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:10518543 735973 Psen1 presenilin 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:22336193 735973 Psen1 presenilin 1 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:22459153 735973 Psen1 presenilin 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 735973 Psen1 presenilin 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:12834865 735973 Psen1 presenilin 1 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21725313 735973 Psen1 presenilin 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12391611 735973 Psen1 presenilin 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10421573 735973 Psen1 presenilin 1 gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12834865 735973 Psen1 presenilin 1 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:22459153 735973 Psen1 presenilin 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:15748844 735973 Psen1 presenilin 1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:15525534 735973 Psen1 presenilin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15525534 735973 Psen1 presenilin 1 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20160421 MGI 735973 Psen1 presenilin 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20160421 MGI 735973 Psen1 presenilin 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10962005 735973 Psen1 presenilin 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:10518543 735973 Psen1 presenilin 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10557208 735973 Psen1 presenilin 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:22336193 735973 Psen1 presenilin 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20160929 MGI PMID:16377636 735973 Psen1 presenilin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10557208 735973 Psen1 presenilin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11738035 735973 Psen1 presenilin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11978821 735973 Psen1 presenilin 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:11102478 735973 Psen1 presenilin 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:15148382 735973 Psen1 presenilin 1 gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:10557208 735973 Psen1 presenilin 1 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11978821 735973 Psen1 presenilin 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:15148382 735973 Psen1 presenilin 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22459153 735973 Psen1 presenilin 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:9883847 735973 Psen1 presenilin 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:10557208 735973 Psen1 presenilin 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:10557208 735973 Psen1 presenilin 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15148382 735973 Psen1 presenilin 1 gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:10421573 735973 Psen1 presenilin 1 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:11262239 735973 Psen1 presenilin 1 gene MP:0003214 neurofibrillary tangles IAGP N RGD:5509061 20141003 MGI PMID:16282321 735973 Psen1 presenilin 1 gene MP:0003214 neurofibrillary tangles IAGP N RGD:5509061 20160929 MGI PMID:16377636 735973 Psen1 presenilin 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:20305648 735973 Psen1 presenilin 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10518543 735973 Psen1 presenilin 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:10518543 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:11102478 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:11567612 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:11959395 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:11978821 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:15466394 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:15748844 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:16282321 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:16307858 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:16597739 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:16963164 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:18585693 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:18974993 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:20693289 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:21725313 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:22459153 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:24278307 735973 Psen1 presenilin 1 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21725313 735973 Psen1 presenilin 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22459153 735973 Psen1 presenilin 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0003385 abnormal body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:10421573 735973 Psen1 presenilin 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:10518543 735973 Psen1 presenilin 1 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:10557208 735973 Psen1 presenilin 1 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:15525534 735973 Psen1 presenilin 1 gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0003414 epidermal cyst IAGP N RGD:5509061 20141003 MGI PMID:15525534 735973 Psen1 presenilin 1 gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:12391611 735973 Psen1 presenilin 1 gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:24278307 735973 Psen1 presenilin 1 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:12834865 735973 Psen1 presenilin 1 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20305648 735973 Psen1 presenilin 1 gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20141003 MGI PMID:10421573 735973 Psen1 presenilin 1 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:10557208 735973 Psen1 presenilin 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:16963164 735973 Psen1 presenilin 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10518543 735973 Psen1 presenilin 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:10518543 735973 Psen1 presenilin 1 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:11262239 735973 Psen1 presenilin 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:10518543 735973 Psen1 presenilin 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:21725313 735973 Psen1 presenilin 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9450754 735973 Psen1 presenilin 1 gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20141003 MGI PMID:24278307 735973 Psen1 presenilin 1 gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20160929 MGI PMID:16377636 735973 Psen1 presenilin 1 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:10557208 735973 Psen1 presenilin 1 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0004546 esophagus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15525534 735973 Psen1 presenilin 1 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:10932180 735973 Psen1 presenilin 1 gene MP:0004605 abnormal vertebral lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:11262239 735973 Psen1 presenilin 1 gene MP:0004605 abnormal vertebral lamina morphology IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0004621 lumbar vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0004622 sacral vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:11262239 735973 Psen1 presenilin 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:11262239 735973 Psen1 presenilin 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:21368062 735973 Psen1 presenilin 1 gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:12391611 735973 Psen1 presenilin 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10421573 735973 Psen1 presenilin 1 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12834865 735973 Psen1 presenilin 1 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:12391611 735973 Psen1 presenilin 1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0005161 hematuria IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16307858 735973 Psen1 presenilin 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16307858 735973 Psen1 presenilin 1 gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:11262239 735973 Psen1 presenilin 1 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:16963164 735973 Psen1 presenilin 1 gene MP:0005412 vascular stenosis IAGP N RGD:5509061 20141003 MGI PMID:12834865 735973 Psen1 presenilin 1 gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:12834865 735973 Psen1 presenilin 1 gene MP:0005623 abnormal meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:10421573 735973 Psen1 presenilin 1 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:10421573 735973 Psen1 presenilin 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:12391611 735973 Psen1 presenilin 1 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:11262239 735973 Psen1 presenilin 1 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12834865 735973 Psen1 presenilin 1 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:10518543 735973 Psen1 presenilin 1 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:21725313 735973 Psen1 presenilin 1 gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:10557208 735973 Psen1 presenilin 1 gene MP:0008029 abnormal paraxial mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:10557208 735973 Psen1 presenilin 1 gene MP:0008031 decreased Cajal-Retzius cell number IAGP N RGD:5509061 20141003 MGI PMID:10421573 735973 Psen1 presenilin 1 gene MP:0008149 abnormal costovertebral joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:9883847 735973 Psen1 presenilin 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:15466394 735973 Psen1 presenilin 1 gene MP:0008286 abnormal hippocampus molecular cell layer IAGP N RGD:5509061 20141003 MGI PMID:15148382 735973 Psen1 presenilin 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:16963164 735973 Psen1 presenilin 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:22336193 735973 Psen1 presenilin 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:22496554 735973 Psen1 presenilin 1 gene MP:0008431 abnormal short-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:21725313 735973 Psen1 presenilin 1 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:11567612 735973 Psen1 presenilin 1 gene MP:0008441 thin cortical plate IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:11262239 735973 Psen1 presenilin 1 gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0008530 abnormal rostral-caudal patterning of the somites IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:15148382 735973 Psen1 presenilin 1 gene MP:0008536 enlarged third ventricle IAGP N RGD:5509061 20141003 MGI PMID:15148382 735973 Psen1 presenilin 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:22459153 735973 Psen1 presenilin 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:18974993 735973 Psen1 presenilin 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22336193 735973 Psen1 presenilin 1 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:24278307 735973 Psen1 presenilin 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:12391611 735973 Psen1 presenilin 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15207348 735973 Psen1 presenilin 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0009938 abnormal hippocampus granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18585693 735973 Psen1 presenilin 1 gene MP:0010052 increased grip strength IAGP N RGD:5509061 20141003 MGI PMID:15908021 735973 Psen1 presenilin 1 gene MP:0010138 arteritis IAGP N RGD:5509061 20141003 MGI PMID:15128703 735973 Psen1 presenilin 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15254914 735973 Psen1 presenilin 1 gene MP:0010459 supravalvar pulmonary trunk stenosis IAGP N RGD:5509061 20141003 MGI PMID:15254914 735973 Psen1 presenilin 1 gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:15525534 735973 Psen1 presenilin 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11262239 735973 Psen1 presenilin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9153393 735973 Psen1 presenilin 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10518543 735973 Psen1 presenilin 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12391611 735973 Psen1 presenilin 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21725313 735973 Psen1 presenilin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10557208 735973 Psen1 presenilin 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21725313 735973 Psen1 presenilin 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9450754 735973 Psen1 presenilin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735973 Psen1 presenilin 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11804702 735973 Psen1 presenilin 1 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20141003 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20160407 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0013380 absent sebocyte IAGP N RGD:5509061 20141218 MGI PMID:15525534 735973 Psen1 presenilin 1 gene MP:0014273 abnormal skin vasculature morphology IAGP N RGD:5509061 20230810 MGI PMID:12834865 735973 Psen1 presenilin 1 gene MP:0014558 decreased cortical ventricular zone thickness IAGP N RGD:5509061 20241031 MGI PMID:25741723 735973 Psen1 presenilin 1 gene MP:0020329 decreased capillary density IAGP N RGD:5509061 20160714 MGI PMID:12834865 735973 Psen1 presenilin 1 gene MP:0021008 temporal lobe atrophy IAGP N RGD:5509061 20210805 MGI PMID:9160754 735973 Psen1 presenilin 1 gene MP:0030286 occipital bone hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:9160754 735974 Trim3 tripartite motif-containing 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 735974 Trim3 tripartite motif-containing 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24086586 735974 Trim3 tripartite motif-containing 3 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:20543135 735974 Trim3 tripartite motif-containing 3 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 735974 Trim3 tripartite motif-containing 3 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 735974 Trim3 tripartite motif-containing 3 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:20543135 735980 Csnk1d casein kinase 1, delta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15800623 735980 Csnk1d casein kinase 1, delta gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:15800623 735980 Csnk1d casein kinase 1, delta gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:19414593 735980 Csnk1d casein kinase 1, delta gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15800623 735980 Csnk1d casein kinase 1, delta gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19414593 735980 Csnk1d casein kinase 1, delta gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19414593 735980 Csnk1d casein kinase 1, delta gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:17218255 735980 Csnk1d casein kinase 1, delta gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:19414593 735980 Csnk1d casein kinase 1, delta gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:17218255 735981 Gmpr guanosine monophosphate reductase gene MP:0005270 abnormal zygomatic bone morphology IEA N RGD:5509061 20201231 MGI 735983 Mitf melanogenesis associated transcription factor gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:8776879 735983 Mitf melanogenesis associated transcription factor gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:7852195 735983 Mitf melanogenesis associated transcription factor gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:11930005 735983 Mitf melanogenesis associated transcription factor gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:4092923 735983 Mitf melanogenesis associated transcription factor gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0000121 failure of tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:11930005 735983 Mitf melanogenesis associated transcription factor gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:6127714 735983 Mitf melanogenesis associated transcription factor gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:15081122 735983 Mitf melanogenesis associated transcription factor gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:16117796 735983 Mitf melanogenesis associated transcription factor gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:22367038 735983 Mitf melanogenesis associated transcription factor gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:8947051 735983 Mitf melanogenesis associated transcription factor gene MP:0000371 diluted coat color IAGP N RGD:5509061 20200220 MGI PMID:18902556 735983 Mitf melanogenesis associated transcription factor gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10790403 735983 Mitf melanogenesis associated transcription factor gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18202372 735983 Mitf melanogenesis associated transcription factor gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:22367038 735983 Mitf melanogenesis associated transcription factor gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9501313 735983 Mitf melanogenesis associated transcription factor gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:10790403 735983 Mitf melanogenesis associated transcription factor gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:15081122 735983 Mitf melanogenesis associated transcription factor gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:22367038 735983 Mitf melanogenesis associated transcription factor gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0000373 belly spot IAGP N RGD:5509061 20180705 MGI PMID:19635938 735983 Mitf melanogenesis associated transcription factor gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:3578491 735983 Mitf melanogenesis associated transcription factor gene MP:0000394 absent hair follicle melanin granules IAGP N RGD:5509061 20150528 MGI PMID:22563733 735983 Mitf melanogenesis associated transcription factor gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:4092923 735983 Mitf melanogenesis associated transcription factor gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:4092923 735983 Mitf melanogenesis associated transcription factor gene MP:0001189 absent skin pigmentation IEA N RGD:5509061 20111116 MGI 735983 Mitf melanogenesis associated transcription factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11930005 735983 Mitf melanogenesis associated transcription factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11930005 735983 Mitf melanogenesis associated transcription factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20200220 MGI PMID:18902556 735983 Mitf melanogenesis associated transcription factor gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:4963367 735983 Mitf melanogenesis associated transcription factor gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:8776879 735983 Mitf melanogenesis associated transcription factor gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10790403 735983 Mitf melanogenesis associated transcription factor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11930005 735983 Mitf melanogenesis associated transcription factor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15081122 735983 Mitf melanogenesis associated transcription factor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:4092923 735983 Mitf melanogenesis associated transcription factor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:4963367 735983 Mitf melanogenesis associated transcription factor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:8513335 735983 Mitf melanogenesis associated transcription factor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:8776879 735983 Mitf melanogenesis associated transcription factor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:9501313 735983 Mitf melanogenesis associated transcription factor gene MP:0001297 microphthalmia IAGP N RGD:5509061 20200220 MGI PMID:18902556 735983 Mitf melanogenesis associated transcription factor gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:8776879 735983 Mitf melanogenesis associated transcription factor gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:8776879 735983 Mitf melanogenesis associated transcription factor gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8776879 735983 Mitf melanogenesis associated transcription factor gene MP:0001324 abnormal eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8947051 735983 Mitf melanogenesis associated transcription factor gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:8947051 735983 Mitf melanogenesis associated transcription factor gene MP:0001333 absent optic nerve IAGP N RGD:5509061 20141003 MGI PMID:4963367 735983 Mitf melanogenesis associated transcription factor gene MP:0001340 abnormal eyelid morphology IEA N RGD:5509061 20111116 MGI 735983 Mitf melanogenesis associated transcription factor gene MP:0001382 abnormal nursing IAGP N RGD:5509061 20141003 MGI PMID:15081122 735983 Mitf melanogenesis associated transcription factor gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:15081122 735983 Mitf melanogenesis associated transcription factor gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20190425 MGI PMID:28666097 735983 Mitf melanogenesis associated transcription factor gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15081122 735983 Mitf melanogenesis associated transcription factor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15081122 735983 Mitf melanogenesis associated transcription factor gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:8776879 735983 Mitf melanogenesis associated transcription factor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20200220 MGI PMID:18902556 735983 Mitf melanogenesis associated transcription factor gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:7852195 735983 Mitf melanogenesis associated transcription factor gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:16117796 735983 Mitf melanogenesis associated transcription factor gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18272592 735983 Mitf melanogenesis associated transcription factor gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:22367038 735983 Mitf melanogenesis associated transcription factor gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11930005 735983 Mitf melanogenesis associated transcription factor gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 735983 Mitf melanogenesis associated transcription factor gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:23028343 735983 Mitf melanogenesis associated transcription factor gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:8776879 735983 Mitf melanogenesis associated transcription factor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190808 MGI PMID:22792072 735983 Mitf melanogenesis associated transcription factor gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:4092923 735983 Mitf melanogenesis associated transcription factor gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:4092923 735983 Mitf melanogenesis associated transcription factor gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20141003 MGI PMID:4092923 735983 Mitf melanogenesis associated transcription factor gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9949161 735983 Mitf melanogenesis associated transcription factor gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8776879 735983 Mitf melanogenesis associated transcription factor gene MP:0002697 abnormal eye size IAGP N RGD:5509061 20141003 MGI PMID:23028343 735983 Mitf melanogenesis associated transcription factor gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:4092923 735983 Mitf melanogenesis associated transcription factor gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20190425 MGI PMID:28666097 735983 Mitf melanogenesis associated transcription factor gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16117796 735983 Mitf melanogenesis associated transcription factor gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22367038 735983 Mitf melanogenesis associated transcription factor gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:3578491 735983 Mitf melanogenesis associated transcription factor gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8513335 735983 Mitf melanogenesis associated transcription factor gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:15081122 735983 Mitf melanogenesis associated transcription factor gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:16117796 735983 Mitf melanogenesis associated transcription factor gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:22367038 735983 Mitf melanogenesis associated transcription factor gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0002938 white spotting IAGP N RGD:5509061 20180705 MGI PMID:19635938 735983 Mitf melanogenesis associated transcription factor gene MP:0002938 white spotting IAGP N RGD:5509061 20221124 MGI PMID:34849815 735983 Mitf melanogenesis associated transcription factor gene MP:0002939 head spot IAGP N RGD:5509061 20141003 MGI PMID:15081122 735983 Mitf melanogenesis associated transcription factor gene MP:0002939 head spot IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0002940 variable body spotting IEA N RGD:5509061 20111116 MGI 735983 Mitf melanogenesis associated transcription factor gene MP:0003053 delayed tooth eruption IAGP N RGD:5509061 20141003 MGI PMID:11930005 735983 Mitf melanogenesis associated transcription factor gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0003099 retina detachment IAGP N RGD:5509061 20141003 MGI PMID:8631625 735983 Mitf melanogenesis associated transcription factor gene MP:0003136 yellow coat color IEA N RGD:5509061 20111116 MGI 735983 Mitf melanogenesis associated transcription factor gene MP:0003169 abnormal scala media morphology IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0003171 phenotypic reversion IAGP N RGD:5509061 20141003 MGI PMID:18202372 735983 Mitf melanogenesis associated transcription factor gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20190425 MGI PMID:28666097 735983 Mitf melanogenesis associated transcription factor gene MP:0003327 liver cyst IAGP N RGD:5509061 20190425 MGI PMID:28666097 735983 Mitf melanogenesis associated transcription factor gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20190425 MGI PMID:28666097 735983 Mitf melanogenesis associated transcription factor gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20141003 MGI PMID:4092923 735983 Mitf melanogenesis associated transcription factor gene MP:0003798 abnormal Harderian gland pigmentation IAGP N RGD:5509061 20150205 MGI PMID:8947051 735983 Mitf melanogenesis associated transcription factor gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:8631625 735983 Mitf melanogenesis associated transcription factor gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20190425 MGI PMID:28666097 735983 Mitf melanogenesis associated transcription factor gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8631625 735983 Mitf melanogenesis associated transcription factor gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:4963367 735983 Mitf melanogenesis associated transcription factor gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:4963367 735983 Mitf melanogenesis associated transcription factor gene MP:0004364 thin stria vascularis IAGP N RGD:5509061 20141003 MGI PMID:7852195 735983 Mitf melanogenesis associated transcription factor gene MP:0004364 thin stria vascularis IAGP N RGD:5509061 20141003 MGI PMID:8776879 735983 Mitf melanogenesis associated transcription factor gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22367038 735983 Mitf melanogenesis associated transcription factor gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8513335 735983 Mitf melanogenesis associated transcription factor gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0004755 abnormal loop of Henle morphology IAGP N RGD:5509061 20190425 MGI PMID:28666097 735983 Mitf melanogenesis associated transcription factor gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:11930005 735983 Mitf melanogenesis associated transcription factor gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:4963367 735983 Mitf melanogenesis associated transcription factor gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:4963367 735983 Mitf melanogenesis associated transcription factor gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0005098 abnormal optic choroid morphology IAGP N RGD:5509061 20141003 MGI PMID:4963367 735983 Mitf melanogenesis associated transcription factor gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20141003 MGI PMID:4963367 735983 Mitf melanogenesis associated transcription factor gene MP:0005100 abnormal choroid pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8947051 735983 Mitf melanogenesis associated transcription factor gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18715234 735983 Mitf melanogenesis associated transcription factor gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8402531 735983 Mitf melanogenesis associated transcription factor gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4963367 735983 Mitf melanogenesis associated transcription factor gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8631625 735983 Mitf melanogenesis associated transcription factor gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9501313 735983 Mitf melanogenesis associated transcription factor gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10790403 735983 Mitf melanogenesis associated transcription factor gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11930005 735983 Mitf melanogenesis associated transcription factor gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15081122 735983 Mitf melanogenesis associated transcription factor gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:18202372 735983 Mitf melanogenesis associated transcription factor gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:22367038 735983 Mitf melanogenesis associated transcription factor gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:3578491 735983 Mitf melanogenesis associated transcription factor gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4092923 735983 Mitf melanogenesis associated transcription factor gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8513335 735983 Mitf melanogenesis associated transcription factor gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8947051 735983 Mitf melanogenesis associated transcription factor gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9949161 735983 Mitf melanogenesis associated transcription factor gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20150528 MGI PMID:22563733 735983 Mitf melanogenesis associated transcription factor gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20200220 MGI PMID:18902556 735983 Mitf melanogenesis associated transcription factor gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10790403 735983 Mitf melanogenesis associated transcription factor gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10886015 735983 Mitf melanogenesis associated transcription factor gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11930005 735983 Mitf melanogenesis associated transcription factor gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4092923 735983 Mitf melanogenesis associated transcription factor gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8776879 735983 Mitf melanogenesis associated transcription factor gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9501313 735983 Mitf melanogenesis associated transcription factor gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20200220 MGI PMID:18902556 735983 Mitf melanogenesis associated transcription factor gene MP:0005172 decreased eye pigmentation IAGP N RGD:5509061 20221124 MGI PMID:34849815 735983 Mitf melanogenesis associated transcription factor gene MP:0005175 non-pigmented tail tip IEA N RGD:5509061 20111116 MGI 735983 Mitf melanogenesis associated transcription factor gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0005195 abnormal posterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:4963367 735983 Mitf melanogenesis associated transcription factor gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:4963367 735983 Mitf melanogenesis associated transcription factor gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:8631625 735983 Mitf melanogenesis associated transcription factor gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20150416 MGI PMID:8947051 735983 Mitf melanogenesis associated transcription factor gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20190808 MGI PMID:22792072 735983 Mitf melanogenesis associated transcription factor gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:8947051 735983 Mitf melanogenesis associated transcription factor gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0005262 coloboma IAGP N RGD:5509061 20141003 MGI PMID:4963367 735983 Mitf melanogenesis associated transcription factor gene MP:0005358 abnormal incisor morphology IEA N RGD:5509061 20111116 MGI 735983 Mitf melanogenesis associated transcription factor gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:3578491 735983 Mitf melanogenesis associated transcription factor gene MP:0005366 variegated coat color IAGP N RGD:5509061 20141003 MGI PMID:18202372 735983 Mitf melanogenesis associated transcription factor gene MP:0005408 hypopigmentation IEA N RGD:5509061 20111116 MGI 735983 Mitf melanogenesis associated transcription factor gene MP:0005409 darkened coat color IAGP N RGD:5509061 20141003 MGI PMID:22367038 735983 Mitf melanogenesis associated transcription factor gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0005541 abnormal iris stromal pigmentation IEA N RGD:5509061 20111116 MGI 735983 Mitf melanogenesis associated transcription factor gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20190425 MGI PMID:28666097 735983 Mitf melanogenesis associated transcription factor gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:6696991 735983 Mitf melanogenesis associated transcription factor gene MP:0006010 absent strial intermediate cells IAGP N RGD:5509061 20141003 MGI PMID:7852195 735983 Mitf melanogenesis associated transcription factor gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:4963367 735983 Mitf melanogenesis associated transcription factor gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0006159 ocular albinism IAGP N RGD:5509061 20200220 MGI PMID:18902556 735983 Mitf melanogenesis associated transcription factor gene MP:0006226 iris hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8402531 735983 Mitf melanogenesis associated transcription factor gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20111116 MGI 735983 Mitf melanogenesis associated transcription factor gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:15081122 735983 Mitf melanogenesis associated transcription factor gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0008447 absent retina cone cells IAGP N RGD:5509061 20141003 MGI PMID:8631625 735983 Mitf melanogenesis associated transcription factor gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:8631625 735983 Mitf melanogenesis associated transcription factor gene MP:0008454 absent retina rod cells IAGP N RGD:5509061 20141003 MGI PMID:8631625 735983 Mitf melanogenesis associated transcription factor gene MP:0008480 absent eye pigmentation IAGP N RGD:5509061 20141003 MGI PMID:10790403 735983 Mitf melanogenesis associated transcription factor gene MP:0008528 polycystic kidney IAGP N RGD:5509061 20190425 MGI PMID:28666097 735983 Mitf melanogenesis associated transcription factor gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:4092923 735983 Mitf melanogenesis associated transcription factor gene MP:0008731 abnormal hair shaft melanin granule morphology IEA N RGD:5509061 20111116 MGI 735983 Mitf melanogenesis associated transcription factor gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:4392283 735983 Mitf melanogenesis associated transcription factor gene MP:0009379 abnormal foot pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0009379 abnormal foot pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9501313 735983 Mitf melanogenesis associated transcription factor gene MP:0009379 abnormal foot pigmentation IAGP N RGD:5509061 20200220 MGI PMID:18902556 735983 Mitf melanogenesis associated transcription factor gene MP:0009772 abnormal retina development IAGP N RGD:5509061 20141003 MGI PMID:4092923 735983 Mitf melanogenesis associated transcription factor gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20150528 MGI PMID:22563733 735983 Mitf melanogenesis associated transcription factor gene MP:0009784 abnormal melanoblast migration IAGP N RGD:5509061 20150528 MGI PMID:22563733 735983 Mitf melanogenesis associated transcription factor gene MP:0009877 exostosis IAGP N RGD:5509061 20141003 MGI PMID:11930005 735983 Mitf melanogenesis associated transcription factor gene MP:0010016 variable depigmentation IAGP N RGD:5509061 20141003 MGI PMID:3578491 735983 Mitf melanogenesis associated transcription factor gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:9949161 735983 Mitf melanogenesis associated transcription factor gene MP:0010932 increased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:7495310 735983 Mitf melanogenesis associated transcription factor gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11930005 735983 Mitf melanogenesis associated transcription factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11930005 735983 Mitf melanogenesis associated transcription factor gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20221124 MGI PMID:34849815 735983 Mitf melanogenesis associated transcription factor gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8947051 735983 Mitf melanogenesis associated transcription factor gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9501313 735983 Mitf melanogenesis associated transcription factor gene MP:0011277 decreased tail pigmentation IAGP N RGD:5509061 20200220 MGI PMID:18902556 735983 Mitf melanogenesis associated transcription factor gene MP:0011279 decreased ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11929848 735983 Mitf melanogenesis associated transcription factor gene MP:0011279 decreased ear pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8947051 735983 Mitf melanogenesis associated transcription factor gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20190425 MGI PMID:28666097 735983 Mitf melanogenesis associated transcription factor gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20190425 MGI PMID:28666097 735983 Mitf melanogenesis associated transcription factor gene MP:0011697 lens vacuoles IEA N RGD:5509061 20141003 MGI 735983 Mitf melanogenesis associated transcription factor gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:7852195 735983 Mitf melanogenesis associated transcription factor gene MP:0012023 decreased melanocyte number IAGP N RGD:5509061 20150528 MGI PMID:22563733 735983 Mitf melanogenesis associated transcription factor gene MP:0012535 abnormal optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:4963367 735983 Mitf melanogenesis associated transcription factor gene MP:0013743 ciliary body hypoplasia IAGP N RGD:5509061 20150416 MGI PMID:8402531 735983 Mitf melanogenesis associated transcription factor gene MP:0014164 abnormal ciliary process morphology IAGP N RGD:5509061 20160414 MGI PMID:8947051 735983 Mitf melanogenesis associated transcription factor gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:8947051 735991 Slc12a3 solute carrier family 12, member 3 gene MP:0001762 polyuria IAGP N RGD:5509061 20230720 MGI PMID:36370249 735991 Slc12a3 solute carrier family 12, member 3 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9786924 735991 Slc12a3 solute carrier family 12, member 3 gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:9786924 735991 Slc12a3 solute carrier family 12, member 3 gene MP:0004119 hypokalemia IAGP N RGD:5509061 20230720 MGI PMID:36370249 735991 Slc12a3 solute carrier family 12, member 3 gene MP:0004757 abnormal distal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:9786924 735991 Slc12a3 solute carrier family 12, member 3 gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20230720 MGI PMID:36370249 735991 Slc12a3 solute carrier family 12, member 3 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:20389022 735991 Slc12a3 solute carrier family 12, member 3 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20389022 735991 Slc12a3 solute carrier family 12, member 3 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20230720 MGI PMID:36370249 735991 Slc12a3 solute carrier family 12, member 3 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:9786924 735991 Slc12a3 solute carrier family 12, member 3 gene MP:0010093 decreased circulating magnesium level IAGP N RGD:5509061 20230720 MGI PMID:36370249 735991 Slc12a3 solute carrier family 12, member 3 gene MP:0011435 increased urine magnesium level IAGP N RGD:5509061 20230720 MGI PMID:36370249 735991 Slc12a3 solute carrier family 12, member 3 gene MP:0011442 abnormal renal sodium ion transport IAGP N RGD:5509061 20141003 MGI PMID:20389022 735991 Slc12a3 solute carrier family 12, member 3 gene MP:0011460 decreased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:20389022 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20160804 MGI PMID:24920669 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:19328205 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0000466 esophageal epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11389134 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0000582 toenail hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:11389134 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:11389134 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:19328205 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:14630633 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16814319 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0001627 abnormal cardiac output IAGP N RGD:5509061 20141003 MGI PMID:16814319 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20160908 MGI PMID:24920669 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11389134 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:11389134 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11389134 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16814319 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20160804 MGI PMID:24920669 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:14630633 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:14630633 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:16814319 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20170601 MGI PMID:27114035 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9891028 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002899 fatigue IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:16814319 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:19328205 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11389134 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:14630633 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003277 increased esophageal papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:11389134 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16814319 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003387 aorta coarctation IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:19328205 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003544 abnormal vascular endothelial cell migration IAGP N RGD:5509061 20160804 MGI PMID:24920669 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20160804 MGI PMID:24920669 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:14630633 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:9891028 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:14630633 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20170601 MGI PMID:27114035 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0003923 abnormal heart left atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:19328205 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20160804 MGI PMID:24920669 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:14630633 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:16814319 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:9891028 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11389134 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:19328205 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20170601 MGI PMID:27114035 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10970890 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16814319 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9891028 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20160804 MGI PMID:24920669 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:14630633 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:16814319 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19328205 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:11389134 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:11389134 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16814319 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:19328205 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0005493 stomach epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11389134 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14630633 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9891028 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20160804 MGI PMID:24920669 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0005665 increased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:19328205 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:14630633 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:16814319 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19328205 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:23395171 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0009105 penis prolapse IAGP N RGD:5509061 20141003 MGI PMID:11389134 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:14630633 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0010469 ascending aorta hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20170601 MGI PMID:27114035 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20170601 MGI PMID:27114035 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:19328205 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9891028 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20160804 MGI PMID:24920669 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19692123 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:16814319 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:16814319 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0021161 increased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0021161 increased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:14630633 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0021163 increased heart left ventricle septal wall thickness IAGP N RGD:5509061 20231109 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0030257 increased tongue papilloma incidence IAGP N RGD:5509061 20171019 MGI PMID:11389134 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:11679415 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:16814319 735992 Atp2a2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:10970890 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19631564 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:18394936 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0003080 increased natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20160630 MGI PMID:25745066 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19631564 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19631564 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:18394936 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:19631564 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19631564 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0008053 abnormal NK cell differentiation IAGP N RGD:5509061 20141218 MGI PMID:21898152 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:19631564 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0010357 increased prostate gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18394936 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19631564 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:19631564 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0020917 decreased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:21898152 735994 Klrk1 killer cell lectin-like receptor subfamily K, member 1 gene MP:0031025 decreased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:19631564 736000 Cpb2 carboxypeptidase B2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12417566 736000 Cpb2 carboxypeptidase B2 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:14521589 736000 Cpb2 carboxypeptidase B2 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12417566 736000 Cpb2 carboxypeptidase B2 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:15383602 736000 Cpb2 carboxypeptidase B2 gene MP:0002472 impaired complement alternative pathway IAGP N RGD:5509061 20141003 MGI PMID:15383602 736000 Cpb2 carboxypeptidase B2 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:11781355 736000 Cpb2 carboxypeptidase B2 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:12417566 736000 Cpb2 carboxypeptidase B2 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:16565485 736000 Cpb2 carboxypeptidase B2 gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:14521589 736000 Cpb2 carboxypeptidase B2 gene MP:0003422 abnormal thrombolysis IAGP N RGD:5509061 20141003 MGI PMID:14521589 736000 Cpb2 carboxypeptidase B2 gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:14521589 736000 Cpb2 carboxypeptidase B2 gene MP:0005571 decreased lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:16565485 736000 Cpb2 carboxypeptidase B2 gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16565485 736000 Cpb2 carboxypeptidase B2 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20141003 MGI PMID:16565485 736000 Cpb2 carboxypeptidase B2 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16565485 736000 Cpb2 carboxypeptidase B2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16565485 736000 Cpb2 carboxypeptidase B2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:14521589 736000 Cpb2 carboxypeptidase B2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15383602 736000 Cpb2 carboxypeptidase B2 gene MP:0011502 parietal capsular epithelium metaplasia IAGP N RGD:5509061 20141003 MGI PMID:15383602 736001 Apcs amyloid P component, serum gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:9389795 736001 Apcs amyloid P component, serum gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:15147569 736001 Apcs amyloid P component, serum gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:15147569 736001 Apcs amyloid P component, serum gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9256275 736001 Apcs amyloid P component, serum gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:15147569 736001 Apcs amyloid P component, serum gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:15147569 736001 Apcs amyloid P component, serum gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11121061 736001 Apcs amyloid P component, serum gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:15147569 736001 Apcs amyloid P component, serum gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:11485329 736001 Apcs amyloid P component, serum gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:15147569 736001 Apcs amyloid P component, serum gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:15147569 736001 Apcs amyloid P component, serum gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:11485329 736001 Apcs amyloid P component, serum gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11121061 736001 Apcs amyloid P component, serum gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11121061 736001 Apcs amyloid P component, serum gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:15147569 736004 Hip1 huntingtin interacting protein 1 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20210826 MGI 736004 Hip1 huntingtin interacting protein 1 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20210722 MGI PMID:15121852 736004 Hip1 huntingtin interacting protein 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12839988 736004 Hip1 huntingtin interacting protein 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:14998932 736004 Hip1 huntingtin interacting protein 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0000239 absent common myeloid progenitor cells IAGP N RGD:5509061 20141003 MGI PMID:14998932 736004 Hip1 huntingtin interacting protein 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12839988 736004 Hip1 huntingtin interacting protein 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:11604514 736004 Hip1 huntingtin interacting protein 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11604514 736004 Hip1 huntingtin interacting protein 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20220519 MGI 736004 Hip1 huntingtin interacting protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12839988 736004 Hip1 huntingtin interacting protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210722 MGI PMID:15121852 736004 Hip1 huntingtin interacting protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210722 MGI PMID:30224518 736004 Hip1 huntingtin interacting protein 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:14998932 736004 Hip1 huntingtin interacting protein 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20210722 MGI PMID:30224518 736004 Hip1 huntingtin interacting protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210722 MGI PMID:15121852 736004 Hip1 huntingtin interacting protein 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:14998932 736004 Hip1 huntingtin interacting protein 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:14998932 736004 Hip1 huntingtin interacting protein 1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210520 MGI 736004 Hip1 huntingtin interacting protein 1 gene MP:0001314 cornea opacity IEA N RGD:5509061 20210520 MGI 736004 Hip1 huntingtin interacting protein 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 736004 Hip1 huntingtin interacting protein 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12839988 736004 Hip1 huntingtin interacting protein 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12839988 736004 Hip1 huntingtin interacting protein 1 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:12839988 736004 Hip1 huntingtin interacting protein 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20210610 MGI PMID:15121852 736004 Hip1 huntingtin interacting protein 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12839988 736004 Hip1 huntingtin interacting protein 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:14998932 736004 Hip1 huntingtin interacting protein 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14998932 736004 Hip1 huntingtin interacting protein 1 gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12839988 736004 Hip1 huntingtin interacting protein 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12839988 736004 Hip1 huntingtin interacting protein 1 gene MP:0002083 premature death IAGP N RGD:5509061 20210722 MGI PMID:15121852 736004 Hip1 huntingtin interacting protein 1 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12839988 736004 Hip1 huntingtin interacting protein 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14998932 736004 Hip1 huntingtin interacting protein 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:14998932 736004 Hip1 huntingtin interacting protein 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11604514 736004 Hip1 huntingtin interacting protein 1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20210520 MGI 736004 Hip1 huntingtin interacting protein 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20141003 MGI PMID:11604514 736004 Hip1 huntingtin interacting protein 1 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0004019 abnormal vitamin homeostasis IAGP N RGD:5509061 20210722 MGI PMID:30224518 736004 Hip1 huntingtin interacting protein 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:15121852 736004 Hip1 huntingtin interacting protein 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20210722 MGI PMID:15121852 736004 Hip1 huntingtin interacting protein 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20210722 MGI PMID:30224518 736004 Hip1 huntingtin interacting protein 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11604514 736004 Hip1 huntingtin interacting protein 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:11604514 736004 Hip1 huntingtin interacting protein 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20210722 MGI PMID:30224518 736004 Hip1 huntingtin interacting protein 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20210722 MGI PMID:30224518 736004 Hip1 huntingtin interacting protein 1 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20210722 MGI PMID:30224518 736004 Hip1 huntingtin interacting protein 1 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20210520 MGI 736004 Hip1 huntingtin interacting protein 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:14998932 736004 Hip1 huntingtin interacting protein 1 gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19647224 736004 Hip1 huntingtin interacting protein 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220519 MGI 736004 Hip1 huntingtin interacting protein 1 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20141003 MGI PMID:14998932 736004 Hip1 huntingtin interacting protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11604514 736004 Hip1 huntingtin interacting protein 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14998932 736004 Hip1 huntingtin interacting protein 1 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20150312 MGI PMID:14998932 736004 Hip1 huntingtin interacting protein 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:11604514 736004 Hip1 huntingtin interacting protein 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:14998932 736004 Hip1 huntingtin interacting protein 1 gene MP:0021012 decreased acetylcholine level IAGP N RGD:5509061 20210805 MGI PMID:30224518 736004 Hip1 huntingtin interacting protein 1 gene MP:0021127 decreased phosphocholine level IAGP N RGD:5509061 20220721 MGI PMID:30224518 736004 Hip1 huntingtin interacting protein 1 gene MP:0030685 decreased cystathionine level IAGP N RGD:5509061 20210722 MGI PMID:30224518 736004 Hip1 huntingtin interacting protein 1 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:14998932 736004 Hip1 huntingtin interacting protein 1 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:15121852 736004 Hip1 huntingtin interacting protein 1 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210722 MGI PMID:30224518 736013 Cpq carboxypeptidase Q gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 736013 Cpq carboxypeptidase Q gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 736013 Cpq carboxypeptidase Q gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220519 MGI 736014 Ahcy S-adenosylhomocysteine hydrolase gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20220106 MGI PMID:30773021 736014 Ahcy S-adenosylhomocysteine hydrolase gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 736014 Ahcy S-adenosylhomocysteine hydrolase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20220106 MGI PMID:30773021 736014 Ahcy S-adenosylhomocysteine hydrolase gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20220106 MGI PMID:30773021 736014 Ahcy S-adenosylhomocysteine hydrolase gene MP:0010052 increased grip strength IEA N RGD:5509061 20201022 MGI 736014 Ahcy S-adenosylhomocysteine hydrolase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 736014 Ahcy S-adenosylhomocysteine hydrolase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 736014 Ahcy S-adenosylhomocysteine hydrolase gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 736019 Asic5 acid-sensing ion channel family member 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20180705 MGI PMID:24663811 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20152175 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10869496 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:10869496 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0001980 abnormal chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:10869496 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0001980 abnormal chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:15033343 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:10954748 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:15033343 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:20152175 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:10954748 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:10954748 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:10954748 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15033343 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 736020 Gnaz guanine nucleotide binding protein, alpha z subunit gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201001 MGI PMID:10954748 736022 App amyloid beta precursor protein gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15921918 736022 App amyloid beta precursor protein gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20211021 MGI 736022 App amyloid beta precursor protein gene MP:0000604 amyloidosis IAGP N RGD:5509061 20150618 MGI PMID:24728269 736022 App amyloid beta precursor protein gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:9461064 736022 App amyloid beta precursor protein gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:21103325 736022 App amyloid beta precursor protein gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:21303697 736022 App amyloid beta precursor protein gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:10200318 736022 App amyloid beta precursor protein gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15147316 736022 App amyloid beta precursor protein gene MP:0000790 abnormal stratification in cerebral cortex IAGP N RGD:5509061 20180222 MGI PMID:28284905 736022 App amyloid beta precursor protein gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:18029196 736022 App amyloid beta precursor protein gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21303697 736022 App amyloid beta precursor protein gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:21303697 736022 App amyloid beta precursor protein gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15921918 736022 App amyloid beta precursor protein gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16244651 736022 App amyloid beta precursor protein gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:19726636 736022 App amyloid beta precursor protein gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20693289 736022 App amyloid beta precursor protein gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20855613 736022 App amyloid beta precursor protein gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:23986861 736022 App amyloid beta precursor protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11050115 736022 App amyloid beta precursor protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17634375 736022 App amyloid beta precursor protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17884188 736022 App amyloid beta precursor protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20140888 736022 App amyloid beta precursor protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7758106 736022 App amyloid beta precursor protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8001115 736022 App amyloid beta precursor protein gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21303697 736022 App amyloid beta precursor protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9461064 736022 App amyloid beta precursor protein gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22336193 736022 App amyloid beta precursor protein gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:24278307 736022 App amyloid beta precursor protein gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:15147316 736022 App amyloid beta precursor protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9461064 736022 App amyloid beta precursor protein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10188929 736022 App amyloid beta precursor protein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17884188 736022 App amyloid beta precursor protein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:24278307 736022 App amyloid beta precursor protein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21303697 736022 App amyloid beta precursor protein gene MP:0001411 spinning IAGP N RGD:5509061 20141003 MGI PMID:9461064 736022 App amyloid beta precursor protein gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17634375 736022 App amyloid beta precursor protein gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:8001115 736022 App amyloid beta precursor protein gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:8001115 736022 App amyloid beta precursor protein gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:10188929 736022 App amyloid beta precursor protein gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15147316 736022 App amyloid beta precursor protein gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17634375 736022 App amyloid beta precursor protein gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17634375 736022 App amyloid beta precursor protein gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:17634375 736022 App amyloid beta precursor protein gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:9461064 736022 App amyloid beta precursor protein gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:22336193 736022 App amyloid beta precursor protein gene MP:0001916 intracerebral hemorrhage IAGP N RGD:5509061 20170713 MGI PMID:28499154 736022 App amyloid beta precursor protein gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:9461064 736022 App amyloid beta precursor protein gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:15147316 736022 App amyloid beta precursor protein gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:8001115 736022 App amyloid beta precursor protein gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20150618 MGI PMID:24728269 736022 App amyloid beta precursor protein gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20141003 MGI PMID:8001115 736022 App amyloid beta precursor protein gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:17634375 736022 App amyloid beta precursor protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15147316 736022 App amyloid beta precursor protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21303697 736022 App amyloid beta precursor protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23986861 736022 App amyloid beta precursor protein gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:22336193 736022 App amyloid beta precursor protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20140888 736022 App amyloid beta precursor protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20693289 736022 App amyloid beta precursor protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20855613 736022 App amyloid beta precursor protein gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:10200318 736022 App amyloid beta precursor protein gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:17634375 736022 App amyloid beta precursor protein gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:20140888 736022 App amyloid beta precursor protein gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:7758106 736022 App amyloid beta precursor protein gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:10200318 736022 App amyloid beta precursor protein gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:8001115 736022 App amyloid beta precursor protein gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:10200318 736022 App amyloid beta precursor protein gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10188929 736022 App amyloid beta precursor protein gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:17634375 736022 App amyloid beta precursor protein gene MP:0002764 short tibia IEA N RGD:5509061 20210128 MGI 736022 App amyloid beta precursor protein gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:17634375 736022 App amyloid beta precursor protein gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:8001115 736022 App amyloid beta precursor protein gene MP:0002798 abnormal active avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:10188929 736022 App amyloid beta precursor protein gene MP:0002801 abnormal long-term object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:15147316 736022 App amyloid beta precursor protein gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10188929 736022 App amyloid beta precursor protein gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20191031 MGI PMID:30902970 736022 App amyloid beta precursor protein gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200514 MGI PMID:31160584 736022 App amyloid beta precursor protein gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:17634375 736022 App amyloid beta precursor protein gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:7758106 736022 App amyloid beta precursor protein gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:11102478 736022 App amyloid beta precursor protein gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:11959395 736022 App amyloid beta precursor protein gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:15147316 736022 App amyloid beta precursor protein gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:15921918 736022 App amyloid beta precursor protein gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:16244651 736022 App amyloid beta precursor protein gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:20693289 736022 App amyloid beta precursor protein gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:24278307 736022 App amyloid beta precursor protein gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20150618 MGI PMID:24728269 736022 App amyloid beta precursor protein gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20180628 MGI PMID:29311134 736022 App amyloid beta precursor protein gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20200514 MGI PMID:31160584 736022 App amyloid beta precursor protein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:10188929 736022 App amyloid beta precursor protein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:21303697 736022 App amyloid beta precursor protein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20150618 MGI PMID:24728269 736022 App amyloid beta precursor protein gene MP:0003354 astrocytosis IAGP N RGD:5509061 20180628 MGI PMID:29311134 736022 App amyloid beta precursor protein gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:24278307 736022 App amyloid beta precursor protein gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:9461064 736022 App amyloid beta precursor protein gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:17884188 736022 App amyloid beta precursor protein gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20141003 MGI PMID:24278307 736022 App amyloid beta precursor protein gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:21103325 736022 App amyloid beta precursor protein gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:19726636 736022 App amyloid beta precursor protein gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:9461064 736022 App amyloid beta precursor protein gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20170105 MGI 736022 App amyloid beta precursor protein gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8798542 736022 App amyloid beta precursor protein gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20200514 MGI PMID:31160584 736022 App amyloid beta precursor protein gene MP:0008222 decreased hippocampal commissure size IAGP N RGD:5509061 20141003 MGI PMID:10200318 736022 App amyloid beta precursor protein gene MP:0008226 decreased anterior commissure size IAGP N RGD:5509061 20141003 MGI PMID:10200318 736022 App amyloid beta precursor protein gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:8001115 736022 App amyloid beta precursor protein gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:22336193 736022 App amyloid beta precursor protein gene MP:0008817 hematoma IAGP N RGD:5509061 20170713 MGI PMID:28499154 736022 App amyloid beta precursor protein gene MP:0008918 microgliosis IAGP N RGD:5509061 20150618 MGI PMID:24728269 736022 App amyloid beta precursor protein gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:21103325 736022 App amyloid beta precursor protein gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:21103325 736022 App amyloid beta precursor protein gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22336193 736022 App amyloid beta precursor protein gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:24278307 736022 App amyloid beta precursor protein gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20150618 MGI PMID:24728269 736022 App amyloid beta precursor protein gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:9461064 736022 App amyloid beta precursor protein gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:23986861 736022 App amyloid beta precursor protein gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:17634375 736022 App amyloid beta precursor protein gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:17884188 736022 App amyloid beta precursor protein gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20140888 736022 App amyloid beta precursor protein gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:7758106 736022 App amyloid beta precursor protein gene MP:0010162 increased brain cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21303697 736022 App amyloid beta precursor protein gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11050115 736022 App amyloid beta precursor protein gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20693289 736022 App amyloid beta precursor protein gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20855613 736022 App amyloid beta precursor protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20693289 736022 App amyloid beta precursor protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9461064 736022 App amyloid beta precursor protein gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23986861 736022 App amyloid beta precursor protein gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20211021 MGI 736022 App amyloid beta precursor protein gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20211021 MGI 736022 App amyloid beta precursor protein gene MP:0012065 increased astrocyte number IAGP N RGD:5509061 20141003 MGI PMID:15921918 736022 App amyloid beta precursor protein gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:17634375 736022 App amyloid beta precursor protein gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:28499154 736022 App amyloid beta precursor protein gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:15147316 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0000161 scoliosis IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0000478 delayed intestine development IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:16571730 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:10559486 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:10559486 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:10559486 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10230788 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10559486 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:10559486 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001051 abnormal somatic motor system morphology IAGP N RGD:5509061 20141003 MGI PMID:15528206 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:12756228 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:12756228 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:12756228 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:21317887 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:15816869 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:10021384 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:11157052 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:14704277 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002083 premature death IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:12756228 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12756228 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:10230788 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:15567863 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15567863 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:12756228 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:15816869 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:15816869 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0002922 decreased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:15816869 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0003153 early eyelid opening IAGP N RGD:5509061 20200123 MGI PMID:21862560 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16043490 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:10559486 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:12486099 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0003622 ischuria IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:12756228 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10559486 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0004609 vertebral fusion IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0004612 fusion of vertebral bodies IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0004613 fusion of vertebral arches IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0004685 calcified intervertebral disk IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0004778 increased macrophage derived foam cell number IAGP N RGD:5509061 20141003 MGI PMID:15567863 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:10230788 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10021384 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11157052 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:16571730 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16043490 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15567863 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0005438 abnormal glycogen homeostasis IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:15816869 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16973441 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12486099 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0006257 abnormal fungiform papillae morphology IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0006392 abnormal nucleus pulposus morphology IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0006394 abnormal vertebral epiphyseal plate morphology IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10021384 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0006414 decreased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11157052 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:21317887 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9806643 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0008113 abnormal macrophage differentiation IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:10559486 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0008721 abnormal chemokine level IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15272135 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15272135 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0009604 increased keratohyalin granule number IAGP N RGD:5509061 20170720 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16571730 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0010033 paraphimosis IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0010715 retina coloboma IAGP N RGD:5509061 20141003 MGI PMID:12756228 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0011079 decreased macrophage cytokine production IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10559486 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12756228 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15375216 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10230788 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10559486 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:14704277 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:16973441 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0011709 increased fibroblast cell migration IAGP N RGD:5509061 20150212 MGI PMID:16973441 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20170420 MGI PMID:23223452 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0012194 decreased keratinocyte migration IAGP N RGD:5509061 20150212 MGI PMID:16973441 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10559486 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0012502 decreased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10230788 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0012502 decreased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10559486 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0012504 increased forebrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10230788 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0012504 increased forebrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10559486 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0012677 absent brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:10559486 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0012701 increased embryonic neuroepithelium apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10230788 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0013176 abnormal tail position or orientation IAGP N RGD:5509061 20220602 MGI PMID:30664861 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16973441 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:17893331 736024 Mapk9 mitogen-activated protein kinase 9 gene MP:0030837 abnormal knee joint morphology IAGP N RGD:5509061 20220602 MGI PMID:30664861 736028 Celsr2 cadherin, EGF LAG seven-pass G-type receptor 2 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:21746835 736028 Celsr2 cadherin, EGF LAG seven-pass G-type receptor 2 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:21746835 736030 Bpifa1 BPI fold containing family A, member 1 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20151231 MGI PMID:25765466 736030 Bpifa1 BPI fold containing family A, member 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:23499554 736030 Bpifa1 BPI fold containing family A, member 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:21514430 736030 Bpifa1 BPI fold containing family A, member 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:23499554 736030 Bpifa1 BPI fold containing family A, member 1 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:23499554 736030 Bpifa1 BPI fold containing family A, member 1 gene MP:0008654 increased interleukin-1 alpha secretion IAGP N RGD:5509061 20141003 MGI PMID:23499554 736030 Bpifa1 BPI fold containing family A, member 1 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:23499554 736030 Bpifa1 BPI fold containing family A, member 1 gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:28513596 736030 Bpifa1 BPI fold containing family A, member 1 gene MP:0031046 increased susceptibility to Orthomyxoviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:28513596 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0000439 enlarged cranium IAGP N RGD:5509061 20141003 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0000829 dilated fourth ventricle IAGP N RGD:5509061 20141003 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20141003 MGI PMID:11927538 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0001317 abnormal pupil morphology IAGP N RGD:5509061 20150611 MGI PMID:12766032 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20181227 MGI 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20150611 MGI PMID:12766032 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20150611 MGI PMID:12766032 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21085708 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20210128 MGI 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:21085708 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0002699 abnormal vitreous body morphology IAGP N RGD:5509061 20141003 MGI PMID:11927538 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11927538 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20150611 MGI PMID:12766032 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0003975 increased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21085708 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11927538 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:21193414 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0005099 abnormal ciliary body morphology IAGP N RGD:5509061 20150611 MGI PMID:12766032 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0005102 abnormal iris pigmentation IEA N RGD:5509061 20181227 MGI 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0005199 abnormal iris pigment epithelium IAGP N RGD:5509061 20150611 MGI PMID:12766032 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:21085708 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:21193414 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0005541 abnormal iris stromal pigmentation IAGP N RGD:5509061 20150611 MGI PMID:12766032 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:12514129 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20211021 MGI 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20150611 MGI PMID:12766032 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0006241 abnormal placement of pupils IEA N RGD:5509061 20181227 MGI 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:21085708 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:21193414 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20181227 MGI 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20181227 MGI 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0010622 abnormal tricuspid valve cusp morphology IAGP N RGD:5509061 20240104 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0011338 abnormal mesangial matrix morphology IAGP N RGD:5509061 20141003 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:15254016 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 736033 Col18a1 collagen, type XVIII, alpha 1 gene MP:0031109 subarachnoid hemorrhage IAGP N RGD:5509061 20200910 MGI PMID:15254016 736035 Asgr2 asialoglycoprotein receptor 2 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7961705 736035 Asgr2 asialoglycoprotein receptor 2 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:8702886 736035 Asgr2 asialoglycoprotein receptor 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7961705 736035 Asgr2 asialoglycoprotein receptor 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18488037 736035 Asgr2 asialoglycoprotein receptor 2 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:18488037 736035 Asgr2 asialoglycoprotein receptor 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18488037 736037 Slc8a2 solute carrier family 8 (sodium/calcium exchanger), member 2 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:12818181 736037 Slc8a2 solute carrier family 8 (sodium/calcium exchanger), member 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12818181 736037 Slc8a2 solute carrier family 8 (sodium/calcium exchanger), member 2 gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:12818181 736037 Slc8a2 solute carrier family 8 (sodium/calcium exchanger), member 2 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:12818181 736037 Slc8a2 solute carrier family 8 (sodium/calcium exchanger), member 2 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:12818181 736037 Slc8a2 solute carrier family 8 (sodium/calcium exchanger), member 2 gene MP:0002921 abnormal post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:12818181 736037 Slc8a2 solute carrier family 8 (sodium/calcium exchanger), member 2 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12818181 736037 Slc8a2 solute carrier family 8 (sodium/calcium exchanger), member 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:12818181 736037 Slc8a2 solute carrier family 8 (sodium/calcium exchanger), member 2 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:12818181 736037 Slc8a2 solute carrier family 8 (sodium/calcium exchanger), member 2 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:12818181 736044 Apoc4 apolipoprotein C-IV gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20170105 MGI 736044 Apoc4 apolipoprotein C-IV gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20210128 MGI 736044 Apoc4 apolipoprotein C-IV gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20201231 MGI 736044 Apoc4 apolipoprotein C-IV gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210128 MGI 736044 Apoc4 apolipoprotein C-IV gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 736044 Apoc4 apolipoprotein C-IV gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 736044 Apoc4 apolipoprotein C-IV gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 736044 Apoc4 apolipoprotein C-IV gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 736044 Apoc4 apolipoprotein C-IV gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20160811 MGI 736045 Minpp1 multiple inositol polyphosphate histidine phosphatase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10938126 736045 Minpp1 multiple inositol polyphosphate histidine phosphatase 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20220224 MGI PMID:33257696 736045 Minpp1 multiple inositol polyphosphate histidine phosphatase 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20220224 MGI PMID:33257696 736045 Minpp1 multiple inositol polyphosphate histidine phosphatase 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20220224 MGI PMID:33257696 736047 Notch2 notch 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0000233 abnormal blood flow velocity IAGP N RGD:5509061 20141003 MGI PMID:18330927 736047 Notch2 notch 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21562564 736047 Notch2 notch 2 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:17080428 736047 Notch2 notch 2 gene MP:0000388 absent hair follicle inner root sheath IAGP N RGD:5509061 20141003 MGI PMID:15525534 736047 Notch2 notch 2 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0000610 cholestasis IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0000611 jaundice IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0000648 absent sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:15525534 736047 Notch2 notch 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:21562564 736047 Notch2 notch 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21562564 736047 Notch2 notch 2 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18155189 736047 Notch2 notch 2 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:21693515 736047 Notch2 notch 2 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19897741 736047 Notch2 notch 2 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:15525534 736047 Notch2 notch 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:15525534 736047 Notch2 notch 2 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15525534 736047 Notch2 notch 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18155189 736047 Notch2 notch 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18330927 736047 Notch2 notch 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18365007 736047 Notch2 notch 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18365007 736047 Notch2 notch 2 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:16397869 736047 Notch2 notch 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:18330927 736047 Notch2 notch 2 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:18365007 736047 Notch2 notch 2 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12730124 736047 Notch2 notch 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:17359302 736047 Notch2 notch 2 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:17359302 736047 Notch2 notch 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:16397869 736047 Notch2 notch 2 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:17658279 736047 Notch2 notch 2 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17261636 736047 Notch2 notch 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:21562564 736047 Notch2 notch 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15525534 736047 Notch2 notch 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18155189 736047 Notch2 notch 2 gene MP:0002083 premature death IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:18330927 736047 Notch2 notch 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:21562564 736047 Notch2 notch 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17261636 736047 Notch2 notch 2 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17261636 736047 Notch2 notch 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15525534 736047 Notch2 notch 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15897231 736047 Notch2 notch 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17366661 736047 Notch2 notch 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18330927 736047 Notch2 notch 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21991352 736047 Notch2 notch 2 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:12753744 736047 Notch2 notch 2 gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:12960298 736047 Notch2 notch 2 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:18365007 736047 Notch2 notch 2 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:21490058 736047 Notch2 notch 2 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:18365007 736047 Notch2 notch 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18365007 736047 Notch2 notch 2 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:18365007 736047 Notch2 notch 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0003109 short femur IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0003109 short femur IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0003109 short femur IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18155189 736047 Notch2 notch 2 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:18155189 736047 Notch2 notch 2 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:17359302 736047 Notch2 notch 2 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:21693515 736047 Notch2 notch 2 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20141003 MGI PMID:15525534 736047 Notch2 notch 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23806616 736047 Notch2 notch 2 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18155189 736047 Notch2 notch 2 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:18635610 736047 Notch2 notch 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10393120 736047 Notch2 notch 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16397869 736047 Notch2 notch 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17359302 736047 Notch2 notch 2 gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0004194 abnormal kidney pelvis morphology IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:18635610 736047 Notch2 notch 2 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:12730124 736047 Notch2 notch 2 gene MP:0004258 abnormal placenta size IAGP N RGD:5509061 20141003 MGI PMID:17359302 736047 Notch2 notch 2 gene MP:0004381 abnormal hair follicle melanocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17080428 736047 Notch2 notch 2 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18724371 736047 Notch2 notch 2 gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0004560 abnormal chorionic plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17359302 736047 Notch2 notch 2 gene MP:0004706 short vertebral body IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0004754 abnormal kidney collecting duct morphology IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21693515 736047 Notch2 notch 2 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0004978 decreased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:12960298 736047 Notch2 notch 2 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:18155189 736047 Notch2 notch 2 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17658279 736047 Notch2 notch 2 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:18724371 736047 Notch2 notch 2 gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18724371 736047 Notch2 notch 2 gene MP:0005083 abnormal biliary tract morphology IAGP N RGD:5509061 20141003 MGI PMID:21490058 736047 Notch2 notch 2 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:18365007 736047 Notch2 notch 2 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:18155189 736047 Notch2 notch 2 gene MP:0005451 abnormal body composition IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:18330927 736047 Notch2 notch 2 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:19897741 736047 Notch2 notch 2 gene MP:0006032 abnormal ureteric bud morphology IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18155189 736047 Notch2 notch 2 gene MP:0008137 absent podocytes IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0008152 decreased diameter of femur IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12753744 736047 Notch2 notch 2 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:12960298 736047 Notch2 notch 2 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:19217325 736047 Notch2 notch 2 gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:12753744 736047 Notch2 notch 2 gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:17261636 736047 Notch2 notch 2 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:12753744 736047 Notch2 notch 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:21562564 736047 Notch2 notch 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:17658279 736047 Notch2 notch 2 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:21991352 736047 Notch2 notch 2 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18155189 736047 Notch2 notch 2 gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20141003 MGI PMID:15525534 736047 Notch2 notch 2 gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:18635610 736047 Notch2 notch 2 gene MP:0009165 abnormal endocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:18635610 736047 Notch2 notch 2 gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:18635610 736047 Notch2 notch 2 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20141003 MGI PMID:21693515 736047 Notch2 notch 2 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20141003 MGI PMID:21693515 736047 Notch2 notch 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0010451 kidney microaneurysm IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0010451 kidney microaneurysm IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0010457 pulmonary artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0010457 pulmonary artery stenosis IAGP N RGD:5509061 20141003 MGI PMID:18330927 736047 Notch2 notch 2 gene MP:0010459 supravalvar pulmonary trunk stenosis IAGP N RGD:5509061 20141003 MGI PMID:18330927 736047 Notch2 notch 2 gene MP:0010463 aorta stenosis IAGP N RGD:5509061 20141003 MGI PMID:18330927 736047 Notch2 notch 2 gene MP:0010711 persistent hyperplastic primary vitreous IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0010933 decreased trabecular bone connectivity density IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0010965 decreased compact bone volume IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0010968 decreased compact bone area IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11861489 736047 Notch2 notch 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18330927 736047 Notch2 notch 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19897741 736047 Notch2 notch 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23806616 736047 Notch2 notch 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10393120 736047 Notch2 notch 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12753744 736047 Notch2 notch 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16397869 736047 Notch2 notch 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17229764 736047 Notch2 notch 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17359302 736047 Notch2 notch 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0011181 increased hematopoietic cell number IAGP N RGD:5509061 20141003 MGI PMID:21562564 736047 Notch2 notch 2 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0011429 absent mesangial cell IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0011441 decreased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0011934 abnormal branching involved in pancreas development IAGP N RGD:5509061 20141003 MGI PMID:18635610 736047 Notch2 notch 2 gene MP:0011935 abnormal pancreatic bud formation IAGP N RGD:5509061 20141003 MGI PMID:18635610 736047 Notch2 notch 2 gene MP:0012537 abnormal hyaloid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:11171333 736047 Notch2 notch 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:10393120 736047 Notch2 notch 2 gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0020039 increased bone ossification IAGP N RGD:5509061 20211021 MGI PMID:28856714 736047 Notch2 notch 2 gene MP:0020080 increased bone mineralization IAGP N RGD:5509061 20161027 MGI PMID:26627824 736047 Notch2 notch 2 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20180607 MGI PMID:28592489 736047 Notch2 notch 2 gene MP:0031074 increased circulating type I collagen C-terminal telopeptide level IAGP N RGD:5509061 20211021 MGI PMID:28856714 736050 Gpx4 glutathione peroxidase 4 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:19417079 736050 Gpx4 glutathione peroxidase 4 gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20161103 MGI PMID:25922076 736050 Gpx4 glutathione peroxidase 4 gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18762024 736050 Gpx4 glutathione peroxidase 4 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:18762024 736050 Gpx4 glutathione peroxidase 4 gene MP:0001147 small testis IAGP N RGD:5509061 20200116 MGI PMID:19783653 736050 Gpx4 glutathione peroxidase 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20200116 MGI PMID:19783653 736050 Gpx4 glutathione peroxidase 4 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18762024 736050 Gpx4 glutathione peroxidase 4 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20200116 MGI PMID:22207760 736050 Gpx4 glutathione peroxidase 4 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200116 MGI PMID:22207760 736050 Gpx4 glutathione peroxidase 4 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18762024 736050 Gpx4 glutathione peroxidase 4 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12745070 736050 Gpx4 glutathione peroxidase 4 gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20141003 MGI PMID:12566075 736050 Gpx4 glutathione peroxidase 4 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:12566075 736050 Gpx4 glutathione peroxidase 4 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20161103 MGI PMID:25922076 736050 Gpx4 glutathione peroxidase 4 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:12566075 736050 Gpx4 glutathione peroxidase 4 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:12745070 736050 Gpx4 glutathione peroxidase 4 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20161103 MGI PMID:25922076 736050 Gpx4 glutathione peroxidase 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12745070 736050 Gpx4 glutathione peroxidase 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20161103 MGI PMID:25922076 736050 Gpx4 glutathione peroxidase 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19417079 736050 Gpx4 glutathione peroxidase 4 gene MP:0001925 male infertility IAGP N RGD:5509061 20200116 MGI PMID:19783653 736050 Gpx4 glutathione peroxidase 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20161103 MGI PMID:25922076 736050 Gpx4 glutathione peroxidase 4 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18762024 736050 Gpx4 glutathione peroxidase 4 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20161103 MGI PMID:25922076 736050 Gpx4 glutathione peroxidase 4 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20161103 MGI PMID:25922076 736050 Gpx4 glutathione peroxidase 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12566075 736050 Gpx4 glutathione peroxidase 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200116 MGI PMID:19783653 736050 Gpx4 glutathione peroxidase 4 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22401858 736050 Gpx4 glutathione peroxidase 4 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:18762024 736050 Gpx4 glutathione peroxidase 4 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20161103 MGI PMID:25922076 736050 Gpx4 glutathione peroxidase 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20200116 MGI PMID:19783653 736050 Gpx4 glutathione peroxidase 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20200116 MGI PMID:19783653 736050 Gpx4 glutathione peroxidase 4 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18762024 736050 Gpx4 glutathione peroxidase 4 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:18762024 736050 Gpx4 glutathione peroxidase 4 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22401858 736050 Gpx4 glutathione peroxidase 4 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:18206984 736050 Gpx4 glutathione peroxidase 4 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20200116 MGI PMID:22207760 736050 Gpx4 glutathione peroxidase 4 gene MP:0003730 abnormal photoreceptor inner segment morphology IAGP N RGD:5509061 20200116 MGI PMID:22207760 736050 Gpx4 glutathione peroxidase 4 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22401858 736050 Gpx4 glutathione peroxidase 4 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20161103 MGI PMID:25922076 736050 Gpx4 glutathione peroxidase 4 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20200116 MGI PMID:19783653 736050 Gpx4 glutathione peroxidase 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200116 MGI PMID:19783653 736050 Gpx4 glutathione peroxidase 4 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200116 MGI PMID:19783653 736050 Gpx4 glutathione peroxidase 4 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:22401858 736050 Gpx4 glutathione peroxidase 4 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:22401858 736050 Gpx4 glutathione peroxidase 4 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20221110 MGI PMID:34794077 736050 Gpx4 glutathione peroxidase 4 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:18206984 736050 Gpx4 glutathione peroxidase 4 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20200116 MGI PMID:19783653 736050 Gpx4 glutathione peroxidase 4 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20200116 MGI PMID:19783653 736050 Gpx4 glutathione peroxidase 4 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:18762024 736050 Gpx4 glutathione peroxidase 4 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:22207760 736050 Gpx4 glutathione peroxidase 4 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200116 MGI PMID:22207760 736050 Gpx4 glutathione peroxidase 4 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20200116 MGI PMID:22207760 736050 Gpx4 glutathione peroxidase 4 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:19417079 736050 Gpx4 glutathione peroxidase 4 gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20161103 MGI PMID:25922076 736050 Gpx4 glutathione peroxidase 4 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:19417079 736050 Gpx4 glutathione peroxidase 4 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20161103 MGI PMID:25922076 736050 Gpx4 glutathione peroxidase 4 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20200116 MGI PMID:19783653 736050 Gpx4 glutathione peroxidase 4 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20141003 MGI PMID:19417079 736050 Gpx4 glutathione peroxidase 4 gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20161103 MGI PMID:25922076 736050 Gpx4 glutathione peroxidase 4 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20161103 MGI PMID:25922076 736050 Gpx4 glutathione peroxidase 4 gene MP:0009709 hydrometra IEA N RGD:5509061 20190808 MGI 736050 Gpx4 glutathione peroxidase 4 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20161103 MGI PMID:25922076 736050 Gpx4 glutathione peroxidase 4 gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:19417079 736050 Gpx4 glutathione peroxidase 4 gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20141003 MGI PMID:19417079 736050 Gpx4 glutathione peroxidase 4 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:22401858 736050 Gpx4 glutathione peroxidase 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18206984 736050 Gpx4 glutathione peroxidase 4 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20161103 MGI PMID:25922076 736050 Gpx4 glutathione peroxidase 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12566075 736050 Gpx4 glutathione peroxidase 4 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18762024 736050 Gpx4 glutathione peroxidase 4 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12745070 736050 Gpx4 glutathione peroxidase 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736050 Gpx4 glutathione peroxidase 4 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22401858 736050 Gpx4 glutathione peroxidase 4 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20240613 MGI PMID:19783653 736050 Gpx4 glutathione peroxidase 4 gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20200116 MGI PMID:22207760 736050 Gpx4 glutathione peroxidase 4 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 736050 Gpx4 glutathione peroxidase 4 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 736050 Gpx4 glutathione peroxidase 4 gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20200116 MGI PMID:22207760 736050 Gpx4 glutathione peroxidase 4 gene MP:0014465 abnormal sperm mitochondrial morphology IAGP N RGD:5509061 20240613 MGI PMID:19783653 736050 Gpx4 glutathione peroxidase 4 gene MP:0014467 increased sperm mitochondrial size IAGP N RGD:5509061 20240613 MGI PMID:19417079 736050 Gpx4 glutathione peroxidase 4 gene MP:0014467 increased sperm mitochondrial size IAGP N RGD:5509061 20240613 MGI PMID:25922076 736052 Fabp7 fatty acid binding protein 7, brain gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:18001149 736052 Fabp7 fatty acid binding protein 7, brain gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:18001149 736052 Fabp7 fatty acid binding protein 7, brain gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16882015 736052 Fabp7 fatty acid binding protein 7, brain gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16882015 736052 Fabp7 fatty acid binding protein 7, brain gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 736052 Fabp7 fatty acid binding protein 7, brain gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:16882015 736052 Fabp7 fatty acid binding protein 7, brain gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16882015 736052 Fabp7 fatty acid binding protein 7, brain gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 736052 Fabp7 fatty acid binding protein 7, brain gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:18001149 736052 Fabp7 fatty acid binding protein 7, brain gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:18001149 736052 Fabp7 fatty acid binding protein 7, brain gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16882015 736053 Ncan neurocan gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11486035 736055 Cyth1 cytohesin 1 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20180503 MGI PMID:23012656 736055 Cyth1 cytohesin 1 gene MP:0013438 dysmyelination IAGP N RGD:5509061 20180503 MGI PMID:23012656 736056 Gzmm granzyme M (lymphocyte met-ase 1) gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:16116214 736059 B3gat1 beta-1,3-glucuronyltransferase 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12032138 736059 B3gat1 beta-1,3-glucuronyltransferase 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12032138 736063 Itgax integrin alpha X gene MP:0001606 impaired hematopoiesis IEA N RGD:5509061 20161201 MGI 736063 Itgax integrin alpha X gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15210787 736063 Itgax integrin alpha X gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15585877 736063 Itgax integrin alpha X gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:17525267 736063 Itgax integrin alpha X gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:20617552 736063 Itgax integrin alpha X gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17525267 736063 Itgax integrin alpha X gene MP:0008127 decreased dendritic cell number IEA N RGD:5509061 20161201 MGI 736063 Itgax integrin alpha X gene MP:0008524 increased plasmacytoid dendritic cell number IEA N RGD:5509061 20161201 MGI 736063 Itgax integrin alpha X gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:17525267 736063 Itgax integrin alpha X gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17525267 736063 Itgax integrin alpha X gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:17525267 736063 Itgax integrin alpha X gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:17525267 736063 Itgax integrin alpha X gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17525267 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:17567819 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17567819 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:17567819 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:11976342 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:11976342 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:20071672 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:11976342 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20171207 MGI PMID:28859131 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0001932 abnormal spermiogenesis IEA N RGD:5509061 20111116 MGI 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20220120 MGI PMID:31727896 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:17567819 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0002229 neurodegeneration IEA N RGD:5509061 20111116 MGI 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20220120 MGI PMID:31727896 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20220120 MGI PMID:31727896 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11976342 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20220120 MGI PMID:31727896 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20171207 MGI PMID:28859131 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0002909 abnormal adrenal gland physiology IAGP N RGD:5509061 20220120 MGI PMID:31727896 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20220120 MGI PMID:31727896 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20150827 MGI PMID:24647135 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17567819 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0003728 abnormal retina photoreceptor layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20071672 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0003729 abnormal photoreceptor outer segment morphology IAGP N RGD:5509061 20141003 MGI PMID:20071672 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:17567819 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20150827 MGI PMID:24647135 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20071672 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20171207 MGI PMID:28859131 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20071672 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:11976342 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:20071672 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0005159 azoospermia IAGP N RGD:5509061 20171207 MGI PMID:28859131 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20071672 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20171207 MGI PMID:28859131 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:17567819 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0005310 abnormal salivary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:11976342 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:17567819 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0005405 axon degeneration IEA N RGD:5509061 20111116 MGI 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20071672 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20220120 MGI PMID:31727896 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11976342 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:17567819 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:20071672 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20150827 MGI PMID:24647135 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20171207 MGI PMID:28859131 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20220120 MGI PMID:31727896 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:17567819 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:11976342 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:20071672 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20171207 MGI PMID:28859131 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:20071672 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:11976342 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0008581 disorganized photoreceptor inner segment IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0008586 disorganized photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:11250895 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20150827 MGI PMID:24647135 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0011460 decreased urine chloride ion level IAGP N RGD:5509061 20220120 MGI PMID:31727896 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20220120 MGI PMID:31727896 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0031384 impaired blood-brain barrier function IAGP N RGD:5509061 20220407 MGI PMID:17567819 736064 Clcn2 chloride channel, voltage-sensitive 2 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:20071672 736069 Coro1b coronin, actin binding protein 1B gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:21844203 736069 Coro1b coronin, actin binding protein 1B gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:21844203 736069 Coro1b coronin, actin binding protein 1B gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:21844203 736069 Coro1b coronin, actin binding protein 1B gene MP:0008764 increased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:21844203 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20170314 MGI PMID:22969701 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20170314 MGI PMID:22969701 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20210128 MGI 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20170314 MGI PMID:22969701 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0004832 enlarged ovary IEA N RGD:5509061 20210128 MGI 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210520 MGI 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210128 MGI 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20170314 MGI PMID:22969701 736073 Btg1 BTG anti-proliferation factor 1 gene MP:0020394 decreased neuronal precursor proliferation IAGP N RGD:5509061 20170314 MGI PMID:22969701 736075 Mvd mevalonate (diphospho) decarboxylase gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 736075 Mvd mevalonate (diphospho) decarboxylase gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 736075 Mvd mevalonate (diphospho) decarboxylase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736075 Mvd mevalonate (diphospho) decarboxylase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 736078 Cst8 cystatin 8 (cystatin-related epididymal spermatogenic) gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220407 MGI PMID:20811015 736078 Cst8 cystatin 8 (cystatin-related epididymal spermatogenic) gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220407 MGI PMID:20811015 736078 Cst8 cystatin 8 (cystatin-related epididymal spermatogenic) gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220407 MGI PMID:20811015 736078 Cst8 cystatin 8 (cystatin-related epididymal spermatogenic) gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20220407 MGI PMID:20811015 736078 Cst8 cystatin 8 (cystatin-related epididymal spermatogenic) gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20220407 MGI PMID:20811015 736078 Cst8 cystatin 8 (cystatin-related epididymal spermatogenic) gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220407 MGI PMID:20811015 736078 Cst8 cystatin 8 (cystatin-related epididymal spermatogenic) gene MP:0004929 decreased epididymis weight IAGP N RGD:5509061 20220407 MGI PMID:20811015 736078 Cst8 cystatin 8 (cystatin-related epididymal spermatogenic) gene MP:0009647 decreased fertilization frequency IAGP N RGD:5509061 20220407 MGI PMID:20811015 736078 Cst8 cystatin 8 (cystatin-related epididymal spermatogenic) gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220407 MGI PMID:20811015 736078 Cst8 cystatin 8 (cystatin-related epididymal spermatogenic) gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20220407 MGI PMID:20811015 736078 Cst8 cystatin 8 (cystatin-related epididymal spermatogenic) gene MP:0031009 abnormal sperm-egg fusion IAGP N RGD:5509061 20220407 MGI PMID:20811015 736079 Lsamp limbic system-associated membrane protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20888367 736079 Lsamp limbic system-associated membrane protein gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20888367 736079 Lsamp limbic system-associated membrane protein gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:18199495 736079 Lsamp limbic system-associated membrane protein gene MP:0001440 abnormal grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:20888367 736079 Lsamp limbic system-associated membrane protein gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:20888367 736079 Lsamp limbic system-associated membrane protein gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20141003 MGI PMID:20888367 736079 Lsamp limbic system-associated membrane protein gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:20888367 736079 Lsamp limbic system-associated membrane protein gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:20888367 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:12782680 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:12093905 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0002188 small heart IAGP N RGD:5509061 20141003 MGI PMID:12782680 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:12782680 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14519431 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0003026 decreased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:12093905 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:12782680 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:12782680 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0003823 increased left ventricle developed pressure IAGP N RGD:5509061 20141003 MGI PMID:14519431 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0003929 decreased heart rate variability IAGP N RGD:5509061 20141003 MGI PMID:12093905 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:14519431 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:12782680 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0004565 decreased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:12782680 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12782680 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20141003 MGI PMID:12782680 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:12782680 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12782680 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0011952 decreased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:12782680 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:12782680 736082 Adra1a adrenergic receptor, alpha 1a gene MP:0031635 increased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:12782680 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:24355923 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:24355923 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:21841138 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11285230 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19147584 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:20147383 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11285230 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:11285230 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:11285230 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:18029401 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:11285230 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:18029401 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:22859719 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19520971 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24355923 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:11285230 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17911384 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:20147383 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0002534 abnormal type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:21998450 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20161124 MGI PMID:26980767 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:21841138 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:19520971 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19147584 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:24355923 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15548578 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18029401 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:11285230 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20190613 MGI PMID:28716756 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:20147383 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0003752 increased oral papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:22859719 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20141003 MGI PMID:20147383 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11285230 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16344855 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18029401 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0004044 aortic dissection IAGP N RGD:5509061 20141003 MGI PMID:24355923 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:16344855 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0004111 abnormal coronary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:24355923 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20141003 MGI PMID:24355923 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22859719 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24124460 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19520971 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0005170 cleft upper lip IAGP N RGD:5509061 20221020 MGI PMID:18586087 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0005243 hemothorax IAGP N RGD:5509061 20141003 MGI PMID:24355923 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:24355923 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:11285230 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:18029401 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16344855 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0006433 abnormal articular cartilage morphology IAGP N RGD:5509061 20190613 MGI PMID:28716756 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20161124 MGI PMID:26980767 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:21998450 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0009053 abnormal anal canal morphology IAGP N RGD:5509061 20141003 MGI PMID:24124460 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20161124 MGI PMID:26980767 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:18586087 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20221020 MGI PMID:18586087 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0010274 increased organ/body region tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24124460 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19147584 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0010661 ascending aorta aneurysm IAGP N RGD:5509061 20141003 MGI PMID:24355923 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:20147383 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0010897 abnormal bronchiole epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20147383 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0010949 decreased club cell number IAGP N RGD:5509061 20141003 MGI PMID:20147383 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20141003 MGI PMID:24355923 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20147383 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15548578 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19147584 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11285230 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16344855 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18029401 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:18586087 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:16344855 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0011572 abnormal aorta bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:24355923 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0011575 dilated aorta bulb IAGP N RGD:5509061 20141003 MGI PMID:24355923 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0011902 increased hematopoietic stem cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12842983 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0012416 decreased gland tumor incidence IAGP N RGD:5509061 20161124 MGI PMID:26980767 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0013304 osteophytes IAGP N RGD:5509061 20190613 MGI PMID:28716756 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20190613 MGI PMID:28716756 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0030343 maxillary prominence hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:18586087 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20171207 MGI PMID:24355923 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0030356 premature lambdoid suture closure IAGP N RGD:5509061 20171207 MGI PMID:24355923 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0030804 abnormal synovial joint morphology IAGP N RGD:5509061 20190613 MGI PMID:28716756 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0031447 unilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:18586087 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0031448 bilateral cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:18586087 736083 Tgfbr1 transforming growth factor, beta receptor I gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20221201 MGI PMID:18586087 736084 Dusp12 dual specificity phosphatase 12 gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20210128 MGI 736084 Dusp12 dual specificity phosphatase 12 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20240314 MGI PMID:36108935 736084 Dusp12 dual specificity phosphatase 12 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20240314 MGI PMID:36108935 736084 Dusp12 dual specificity phosphatase 12 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20240314 MGI PMID:36108935 736084 Dusp12 dual specificity phosphatase 12 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20240314 MGI PMID:36108935 736084 Dusp12 dual specificity phosphatase 12 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20240314 MGI PMID:36108935 736084 Dusp12 dual specificity phosphatase 12 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20240314 MGI PMID:36108935 736084 Dusp12 dual specificity phosphatase 12 gene MP:0010633 myocardium hypertrophy IAGP N RGD:5509061 20240314 MGI PMID:36108935 736084 Dusp12 dual specificity phosphatase 12 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736084 Dusp12 dual specificity phosphatase 12 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 736084 Dusp12 dual specificity phosphatase 12 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20065162 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:20065162 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21803853 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0003290 intestinal hypoperistalsis IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0004548 dilated esophagus IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:21803853 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:20065162 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:21803853 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0006001 abnormal intestinal transit time IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20065162 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0009343 dilated gallbladder IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0009476 enlarged cecum IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0009480 distended cecum IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:21803853 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17452643 736088 Gucy1b1 guanylate cyclase 1, soluble, beta 1 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201002 MGI PMID:21803853 736089 Dgkb diacylglycerol kinase, beta gene MP:0001399 hyperactivity IEA N RGD:5509061 20220428 MGI 736089 Dgkb diacylglycerol kinase, beta gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:20657643 736089 Dgkb diacylglycerol kinase, beta gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:20657643 736089 Dgkb diacylglycerol kinase, beta gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20150312 MGI PMID:22590645 736089 Dgkb diacylglycerol kinase, beta gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20150312 MGI PMID:22590645 736089 Dgkb diacylglycerol kinase, beta gene MP:0005333 decreased heart rate IEA N RGD:5509061 20231207 MGI 736089 Dgkb diacylglycerol kinase, beta gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:20657643 736089 Dgkb diacylglycerol kinase, beta gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:20657643 736089 Dgkb diacylglycerol kinase, beta gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20657643 736089 Dgkb diacylglycerol kinase, beta gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20150312 MGI PMID:22590645 736089 Dgkb diacylglycerol kinase, beta gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20657643 736089 Dgkb diacylglycerol kinase, beta gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 736089 Dgkb diacylglycerol kinase, beta gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22590645 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20180614 MGI PMID:29078393 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0000751 myopathy IAGP N RGD:5509061 20180315 MGI PMID:26929074 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180315 MGI PMID:26929074 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0002083 premature death IAGP N RGD:5509061 20180315 MGI PMID:26929074 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0002188 small heart IAGP N RGD:5509061 20180614 MGI PMID:29078393 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20180315 MGI PMID:26929074 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0002297 abnormal forced expiratory flow rates IAGP N RGD:5509061 20180315 MGI PMID:26929074 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20180315 MGI PMID:26929074 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20180614 MGI PMID:29078393 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20180315 MGI PMID:26929074 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20180614 MGI PMID:29078393 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20180531 MGI PMID:26929074 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20180614 MGI PMID:29078393 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0004783 abnormal cardinal vein morphology IAGP N RGD:5509061 20180614 MGI PMID:29078393 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20180614 MGI PMID:29078393 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20180614 MGI PMID:29078393 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20180315 MGI PMID:26929074 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20180315 MGI PMID:26929074 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20180315 MGI PMID:26929074 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20180315 MGI PMID:26929074 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0010580 decreased heart left ventricle size IAGP N RGD:5509061 20180614 MGI PMID:29078393 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20180315 MGI PMID:26929074 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20180614 MGI PMID:29078393 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20180614 MGI PMID:29078393 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0021160 decreased heart right ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:29078393 736092 Hspb7 heat shock protein family, member 7 (cardiovascular) gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:29078393 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230119 MGI 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0000774 decreased brain size IEA N RGD:5509061 20230119 MGI 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230119 MGI 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0001147 small testis IEA N RGD:5509061 20230119 MGI 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230119 MGI 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20230119 MGI 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21670066 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230119 MGI 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20230119 MGI 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:21670066 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22406547 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230119 MGI 736094 Rtn4rl2 reticulon 4 receptor-like 2 gene MP:0030013 enhanced central nervous system regeneration IAGP N RGD:5509061 20170713 MGI PMID:22406547 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20210520 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0000277 abnormal heart shape IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0000470 abnormal stomach morphology IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0000599 enlarged liver IEA N RGD:5509061 20210826 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0001596 hypotension IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0001762 polyuria IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0001762 polyuria IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0001944 abnormal pancreas morphology IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0002083 premature death IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0002188 small heart IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20201022 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20221215 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0002829 abnormal juxtaglomerular apparatus morphology IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0002834 decreased heart weight IEA N RGD:5509061 20201022 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0002989 small kidney IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0003020 decreased circulating chloride level IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0003028 alkalosis IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0003029 alkalemia IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20190502 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0003900 shortened QT interval IEA N RGD:5509061 20240523 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0003960 increased lean body mass IEA N RGD:5509061 20190502 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0004119 hypokalemia IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0004757 abnormal distal convoluted tubule morphology IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20201022 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20201022 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20201022 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20201022 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20181227 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0005628 decreased circulating potassium level IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0006316 increased urine sodium level IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0009051 dilated distal convoluted tubule IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20190502 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20201022 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0010128 hypovolemia IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0010393 shortened QRS complex duration IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0011301 juxtaglomerular cell hyperplasia IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0011312 abnormal kidney afferent arteriole morphology IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0011313 abnormal kidney efferent arteriole morphology IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0011344 abnormal loop of Henle ascending limb thick segment morphology IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0011417 abnormal renal transport IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0011435 increased urine magnesium level IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0011442 abnormal renal sodium ion transport IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0011459 increased urine chloride ion level IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0011563 increased urine prostaglandin level IAGP N RGD:5509061 20180927 MGI PMID:27421685 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0011563 increased urine prostaglandin level IAGP N RGD:5509061 20181011 MGI PMID:27335120 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210128 MGI 736096 Clcnkb chloride channel, voltage-sensitive Kb gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 736107 Zc3hav1 zinc finger CCCH type, antiviral 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20160526 MGI PMID:23836649 736109 Nup153 nucleoporin 153 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20201022 MGI 736109 Nup153 nucleoporin 153 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 736109 Nup153 nucleoporin 153 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 736109 Nup153 nucleoporin 153 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20220811 MGI 736109 Nup153 nucleoporin 153 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736109 Nup153 nucleoporin 153 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 736111 Stx1b syntaxin 1B gene MP:0001265 decreased body size IAGP N RGD:5509061 20141218 MGI PMID:24587181 736111 Stx1b syntaxin 1B gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18703708 736111 Stx1b syntaxin 1B gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:18703708 736111 Stx1b syntaxin 1B gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18703708 736111 Stx1b syntaxin 1B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18703708 736111 Stx1b syntaxin 1B gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:18703708 736111 Stx1b syntaxin 1B gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141218 MGI PMID:24587181 736111 Stx1b syntaxin 1B gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18703708 736111 Stx1b syntaxin 1B gene MP:0002885 abnormal AMPA-mediated synaptic currents IAGP N RGD:5509061 20141218 MGI PMID:24587181 736111 Stx1b syntaxin 1B gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18703708 736111 Stx1b syntaxin 1B gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141218 MGI PMID:24587181 736111 Stx1b syntaxin 1B gene MP:0004008 abnormal GABA-mediated receptor currents IAGP N RGD:5509061 20141218 MGI PMID:24587181 736111 Stx1b syntaxin 1B gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:18703708 736111 Stx1b syntaxin 1B gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141218 MGI PMID:24587181 736111 Stx1b syntaxin 1B gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141003 MGI PMID:18703708 736111 Stx1b syntaxin 1B gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20141218 MGI PMID:24587181 736111 Stx1b syntaxin 1B gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141218 MGI PMID:24587181 736111 Stx1b syntaxin 1B gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20141218 MGI PMID:24587181 736111 Stx1b syntaxin 1B gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18703708 736111 Stx1b syntaxin 1B gene MP:0008504 abnormal adrenal chromaffin cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18703708 736111 Stx1b syntaxin 1B gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20141218 MGI PMID:24587181 736111 Stx1b syntaxin 1B gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141218 MGI PMID:24587181 736111 Stx1b syntaxin 1B gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141218 MGI PMID:24587181 736111 Stx1b syntaxin 1B gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141218 MGI PMID:24587181 736111 Stx1b syntaxin 1B gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20141218 MGI PMID:24587181 736111 Stx1b syntaxin 1B gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:24587181 736111 Stx1b syntaxin 1B gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:24587181 736117 Rab26 RAB26, member RAS oncogene family gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20230119 MGI 736117 Rab26 RAB26, member RAS oncogene family gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20210722 MGI PMID:29965781 736117 Rab26 RAB26, member RAS oncogene family gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20210722 MGI PMID:29965781 736117 Rab26 RAB26, member RAS oncogene family gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20210722 MGI PMID:29965781 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19721697 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20160811 MGI 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:10704394 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:10704394 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10704394 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:10704394 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15374821 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22460952 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19721697 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:22460952 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10704394 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:22460952 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12150932 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20160811 MGI 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22460952 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0003393 decreased cardiac output IEA N RGD:5509061 20190502 MGI 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0003733 abnormal retina inner nuclear layer morphology IEA N RGD:5509061 20220811 MGI 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10704394 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20180111 MGI PMID:24162845 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19721697 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20180111 MGI PMID:24162845 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22460952 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20210128 MGI 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:10704394 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0008579 abnormal Purkinje cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:10704394 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19721697 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:15374821 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:15374821 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20180111 MGI PMID:24162845 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20161201 MGI 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19721697 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22460952 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0011016 increased core body temperature IAGP N RGD:5509061 20180111 MGI PMID:24162845 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0011020 abnormal circadian temperature homeostasis IAGP N RGD:5509061 20180111 MGI PMID:24162845 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22460952 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20220811 MGI 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0011960 abnormal eye anterior chamber depth IEA N RGD:5509061 20201231 MGI 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0020468 abnormal circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:23471982 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:12150932 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:22460952 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0020474 advanced circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:12150932 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0020523 decreased susceptibility to induced hypothermia IAGP N RGD:5509061 20180125 MGI PMID:24162845 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 736119 Nr1d1 nuclear receptor subfamily 1, group D, member 1 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20180111 MGI PMID:24162845 736121 Vamp1 vesicle-associated membrane protein 1 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 736121 Vamp1 vesicle-associated membrane protein 1 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:17102983 736121 Vamp1 vesicle-associated membrane protein 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:17102983 736121 Vamp1 vesicle-associated membrane protein 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:17102983 736121 Vamp1 vesicle-associated membrane protein 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17102983 736121 Vamp1 vesicle-associated membrane protein 1 gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:17102983 736121 Vamp1 vesicle-associated membrane protein 1 gene MP:0011085 postnatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 736124 Ppp3r2 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type II) gene MP:0001925 male infertility IAGP N RGD:5509061 20160818 MGI PMID:26429887 736124 Ppp3r2 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type II) gene MP:0009282 decreased hyperactivated sperm motility IAGP N RGD:5509061 20160818 MGI PMID:26429887 736124 Ppp3r2 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type II) gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20160818 MGI PMID:26429887 736124 Ppp3r2 protein phosphatase 3, regulatory subunit B, alpha isoform (calcineurin B, type II) gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 736129 Timm10b translocase of inner mitochondrial membrane 10B gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 736130 Ggt5 gamma-glutamyltransferase 5 gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:11463821 736130 Ggt5 gamma-glutamyltransferase 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11463821 736130 Ggt5 gamma-glutamyltransferase 5 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:11463821 736130 Ggt5 gamma-glutamyltransferase 5 gene MP:0001937 abnormal sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:11463821 736130 Ggt5 gamma-glutamyltransferase 5 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:11463821 736130 Ggt5 gamma-glutamyltransferase 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11463821 736130 Ggt5 gamma-glutamyltransferase 5 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:11463821 736131 Tac2 tachykinin 2 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20160407 MGI PMID:25574869 736131 Tac2 tachykinin 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20160407 MGI PMID:25574869 736131 Tac2 tachykinin 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20160407 MGI PMID:25574869 736131 Tac2 tachykinin 2 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20160407 MGI PMID:25574869 736131 Tac2 tachykinin 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20160407 MGI PMID:25574869 736131 Tac2 tachykinin 2 gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20160407 MGI PMID:25574869 736131 Tac2 tachykinin 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 736131 Tac2 tachykinin 2 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20160407 MGI PMID:25574869 736131 Tac2 tachykinin 2 gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20160407 MGI PMID:25574869 736131 Tac2 tachykinin 2 gene MP:0003377 late onset of menarche IAGP N RGD:5509061 20160407 MGI PMID:25574869 736131 Tac2 tachykinin 2 gene MP:0003550 short perineum IAGP N RGD:5509061 20160407 MGI PMID:25574869 736131 Tac2 tachykinin 2 gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20240613 MGI PMID:31405606 736131 Tac2 tachykinin 2 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20160407 MGI PMID:25574869 736131 Tac2 tachykinin 2 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20160407 MGI PMID:25574869 736131 Tac2 tachykinin 2 gene MP:0009020 prolonged metestrus IAGP N RGD:5509061 20160407 MGI PMID:25574869 736131 Tac2 tachykinin 2 gene MP:0010073 decreased pruritus IAGP N RGD:5509061 20240613 MGI PMID:31405606 736132 Prdx6 peroxiredoxin 6 gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14644414 736132 Prdx6 peroxiredoxin 6 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160915 MGI PMID:24652767 736132 Prdx6 peroxiredoxin 6 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0002271 abnormal pulmonary alveolar duct morphology IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0004777 abnormal phospholipid level IAGP N RGD:5509061 20170105 MGI PMID:26921317 736132 Prdx6 peroxiredoxin 6 gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20170105 MGI PMID:26921317 736132 Prdx6 peroxiredoxin 6 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0010857 pulmonary necrosis IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0010858 pulmonary epithelial necrosis IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0010894 pulmonary alveolar edema IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0010909 pulmonary alveolar hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0031158 abnormal venous thrombosis IAGP N RGD:5509061 20201210 MGI PMID:12732627 736132 Prdx6 peroxiredoxin 6 gene MP:0031161 abnormal kidney venous thrombosis IAGP N RGD:5509061 20201210 MGI PMID:12732627 736135 Pigl phosphatidylinositol glycan anchor biosynthesis, class L gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 736135 Pigl phosphatidylinositol glycan anchor biosynthesis, class L gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 736135 Pigl phosphatidylinositol glycan anchor biosynthesis, class L gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20200402 MGI 736135 Pigl phosphatidylinositol glycan anchor biosynthesis, class L gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 736135 Pigl phosphatidylinositol glycan anchor biosynthesis, class L gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 736135 Pigl phosphatidylinositol glycan anchor biosynthesis, class L gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736135 Pigl phosphatidylinositol glycan anchor biosynthesis, class L gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 736137 Ass1 argininosuccinate synthetase 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0000422 delayed hair appearance IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23785515 736137 Ass1 argininosuccinate synthetase 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 736137 Ass1 argininosuccinate synthetase 1 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0002082 postnatal lethality IEA N RGD:5509061 20111116 MGI 736137 Ass1 argininosuccinate synthetase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23785515 736137 Ass1 argininosuccinate synthetase 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0003704 abnormal hair follicle development IEA N RGD:5509061 20111116 MGI 736137 Ass1 argininosuccinate synthetase 1 gene MP:0003809 abnormal hair shaft morphology IEA N RGD:5509061 20181129 MGI 736137 Ass1 argininosuccinate synthetase 1 gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:8197477 736137 Ass1 argininosuccinate synthetase 1 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:23785515 736137 Ass1 argininosuccinate synthetase 1 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:8197477 736137 Ass1 argininosuccinate synthetase 1 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:23785515 736137 Ass1 argininosuccinate synthetase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0010387 abnormal Bergmann glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23785515 736137 Ass1 argininosuccinate synthetase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8197477 736137 Ass1 argininosuccinate synthetase 1 gene MP:0020836 increased circulating citrulline level IAGP N RGD:5509061 20180712 MGI PMID:20724589 736137 Ass1 argininosuccinate synthetase 1 gene MP:0020836 increased circulating citrulline level IAGP N RGD:5509061 20180712 MGI PMID:8197477 736137 Ass1 argininosuccinate synthetase 1 gene MP:0020836 increased circulating citrulline level IAGP N RGD:5509061 20180913 MGI PMID:23785515 736137 Ass1 argininosuccinate synthetase 1 gene MP:0030638 increased circulating taurine level IAGP N RGD:5509061 20180913 MGI PMID:23785515 736137 Ass1 argininosuccinate synthetase 1 gene MP:0030639 decreased circulating taurine level IAGP N RGD:5509061 20180913 MGI PMID:23785515 736137 Ass1 argininosuccinate synthetase 1 gene MP:0030650 increased circulating ornithine level IAGP N RGD:5509061 20180913 MGI PMID:23785515 736137 Ass1 argininosuccinate synthetase 1 gene MP:0030651 decreased circulating ornithine level IAGP N RGD:5509061 20180913 MGI PMID:23785515 736137 Ass1 argininosuccinate synthetase 1 gene MP:0030662 decreased circulating arginine level IAGP N RGD:5509061 20180913 MGI PMID:23785515 736137 Ass1 argininosuccinate synthetase 1 gene MP:0030662 decreased circulating arginine level IAGP N RGD:5509061 20180920 MGI PMID:8197477 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000300 thin atrioventricular cushion IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9637684 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000645 absent adrenergic chromaffin cells IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000645 absent adrenergic chromaffin cells IAGP N RGD:5509061 20141003 MGI PMID:9637684 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:16991114 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000841 abnormal hindbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000844 abnormal pontine flexure morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000856 abnormal cerebellar plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000865 absent cerebellum vermis IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15044753 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:18760695 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141030 MGI PMID:24493648 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16991114 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:20410128 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001007 abnormal sympathetic system morphology IAGP N RGD:5509061 20141003 MGI PMID:9637684 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001008 abnormal sympathetic ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9637684 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9637684 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:9637684 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001045 abnormal enteric ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001065 abnormal trigeminal nerve morphology IEA N RGD:5509061 20111116 MGI 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001077 abnormal spinal nerve morphology IEA N RGD:5509061 20111116 MGI 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001105 abnormal PNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001108 absent Schwann cells IAGP N RGD:5509061 20141003 MGI PMID:16991114 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001108 absent Schwann cells IAGP N RGD:5509061 20141030 MGI PMID:24493648 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001109 absent Schwann cell precursors IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22665265 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:22665265 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001633 poor circulation IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22665265 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19690388 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16991114 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19690388 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0002200 abnormal brain ventricular system morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:16991114 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:9637684 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:20410128 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0004203 abnormal cranial flexure morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:15044753 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:18773073 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0006046 atrioventricular valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:22665265 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:22665265 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0008011 intestine polyps IAGP N RGD:5509061 20141003 MGI PMID:19690388 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0008316 abnormal prevertebral ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9637684 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0008317 abnormal paravertebral ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9637684 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:19690388 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:20410128 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:22665265 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0009504 abnormal mammary gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22665265 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:22665265 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:22665265 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0009798 abnormal ophthalmic nerve morphology IEA N RGD:5509061 20111116 MGI 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0009800 abnormal mandibular nerve morphology IEA N RGD:5509061 20111116 MGI 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:22665265 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141030 MGI PMID:24493648 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22665265 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18760695 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19690388 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9362461 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18773073 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19690388 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16991114 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18773073 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9338783 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18773073 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19690388 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22665265 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0011731 decreased myelin sheath thickness IAGP N RGD:5509061 20141030 MGI PMID:24493648 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:9637684 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0013716 hypolactation IAGP N RGD:5509061 20150402 MGI PMID:22665265 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0014126 increased mammary gland apoptosis IAGP N RGD:5509061 20160317 MGI PMID:22665265 736142 Erbb3 erb-b2 receptor tyrosine kinase 3 gene MP:0031550 abnormal atrioventricular valve development IAGP N RGD:5509061 20240104 MGI PMID:9362461 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20200416 MGI PMID:31402636 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20220106 MGI PMID:25512563 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20200416 MGI PMID:31402636 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20200416 MGI PMID:31402636 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20200416 MGI PMID:31402636 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20220106 MGI PMID:25512563 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20200416 MGI PMID:31402636 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20200416 MGI PMID:31402636 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20220106 MGI PMID:25512563 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20200416 MGI PMID:31402636 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20220106 MGI PMID:25512563 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0011709 increased fibroblast cell migration IAGP N RGD:5509061 20200416 MGI PMID:31402636 736144 Arhgef7 Rho guanine nucleotide exchange factor gene MP:0020416 decreased fibroblast chemotaxis IAGP N RGD:5509061 20200416 MGI PMID:31402636 736146 Fbln5 fibulin 5 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11805834 736146 Fbln5 fibulin 5 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:15710889 736146 Fbln5 fibulin 5 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:11805834 736146 Fbln5 fibulin 5 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:11805835 736146 Fbln5 fibulin 5 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:11805835 736146 Fbln5 fibulin 5 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:11805835 736146 Fbln5 fibulin 5 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11805834 736146 Fbln5 fibulin 5 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11805835 736146 Fbln5 fibulin 5 gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:20197418 736146 Fbln5 fibulin 5 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:11805834 736146 Fbln5 fibulin 5 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:11805835 736146 Fbln5 fibulin 5 gene MP:0002268 abnormal terminal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:11805834 736146 Fbln5 fibulin 5 gene MP:0002268 abnormal terminal bronchiole morphology IAGP N RGD:5509061 20141003 MGI PMID:11805835 736146 Fbln5 fibulin 5 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:11805834 736146 Fbln5 fibulin 5 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:11805835 736146 Fbln5 fibulin 5 gene MP:0002295 abnormal pulmonary circulation IAGP N RGD:5509061 20141003 MGI PMID:11805834 736146 Fbln5 fibulin 5 gene MP:0002295 abnormal pulmonary circulation IAGP N RGD:5509061 20141003 MGI PMID:11805835 736146 Fbln5 fibulin 5 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11805835 736146 Fbln5 fibulin 5 gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11805834 736146 Fbln5 fibulin 5 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:20197418 736146 Fbln5 fibulin 5 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:20197418 736146 Fbln5 fibulin 5 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:15710889 736146 Fbln5 fibulin 5 gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:11805834 736146 Fbln5 fibulin 5 gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:11805835 736146 Fbln5 fibulin 5 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:15710889 736146 Fbln5 fibulin 5 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20197418 736146 Fbln5 fibulin 5 gene MP:0006083 abnormal blood vessel elastic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:15710889 736146 Fbln5 fibulin 5 gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:11805834 736146 Fbln5 fibulin 5 gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:11805834 736146 Fbln5 fibulin 5 gene MP:0010464 abnormal aortic arch and aortic arch branch attachment IAGP N RGD:5509061 20141003 MGI PMID:11805834 736146 Fbln5 fibulin 5 gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:15710889 736148 Itga8 integrin alpha 8 gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20210128 MGI 736148 Itga8 integrin alpha 8 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:17537792 736148 Itga8 integrin alpha 8 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:9054500 736148 Itga8 integrin alpha 8 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:17537792 736148 Itga8 integrin alpha 8 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:9054500 736148 Itga8 integrin alpha 8 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:9054500 736148 Itga8 integrin alpha 8 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:12904471 736148 Itga8 integrin alpha 8 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12904471 736148 Itga8 integrin alpha 8 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:20132319 736148 Itga8 integrin alpha 8 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:10742111 736148 Itga8 integrin alpha 8 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20210826 MGI 736148 Itga8 integrin alpha 8 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:20132319 736148 Itga8 integrin alpha 8 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17537792 736148 Itga8 integrin alpha 8 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:9054500 736148 Itga8 integrin alpha 8 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 736148 Itga8 integrin alpha 8 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:17537792 736148 Itga8 integrin alpha 8 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:9054500 736148 Itga8 integrin alpha 8 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:19769957 736148 Itga8 integrin alpha 8 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19769957 736148 Itga8 integrin alpha 8 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:19769957 736148 Itga8 integrin alpha 8 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:9054500 736148 Itga8 integrin alpha 8 gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:9054500 736148 Itga8 integrin alpha 8 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:9054500 736148 Itga8 integrin alpha 8 gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:10742111 736148 Itga8 integrin alpha 8 gene MP:0004516 fused vestibular hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:10742111 736148 Itga8 integrin alpha 8 gene MP:0004517 decreased vestibular hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:10742111 736148 Itga8 integrin alpha 8 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10742111 736148 Itga8 integrin alpha 8 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20210128 MGI 736148 Itga8 integrin alpha 8 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20210128 MGI 736148 Itga8 integrin alpha 8 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20211021 MGI 736148 Itga8 integrin alpha 8 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 736148 Itga8 integrin alpha 8 gene MP:0010818 adhesive atelectasis IAGP N RGD:5509061 20141003 MGI PMID:19769957 736148 Itga8 integrin alpha 8 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:19769957 736148 Itga8 integrin alpha 8 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:19769957 736148 Itga8 integrin alpha 8 gene MP:0010977 fused right lung lobes IAGP N RGD:5509061 20141003 MGI PMID:19769957 736148 Itga8 integrin alpha 8 gene MP:0010983 abnormal ureteric bud invasion IAGP N RGD:5509061 20141003 MGI PMID:10742111 736148 Itga8 integrin alpha 8 gene MP:0011011 impaired lung lobe morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19769957 736148 Itga8 integrin alpha 8 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:19769957 736148 Itga8 integrin alpha 8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19769957 736148 Itga8 integrin alpha 8 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9054500 736148 Itga8 integrin alpha 8 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0008259 abnormal optic disk morphology IEA N RGD:5509061 20210520 MGI 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0008559 abnormal interferon-gamma secretion IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0010926 increased osteoid volume IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0010929 increased osteoid thickness IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20201112 MGI PMID:31295380 736151 Dpp3 dipeptidylpeptidase 3 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20201112 MGI PMID:31295380 736153 Gbp2 guanylate binding protein 2 gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20220811 MGI 736153 Gbp2 guanylate binding protein 2 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:23248289 736153 Gbp2 guanylate binding protein 2 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20220811 MGI 736153 Gbp2 guanylate binding protein 2 gene MP:0010750 increased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23248289 736153 Gbp2 guanylate binding protein 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 736155 Pak3 p21 (RAC1) activated kinase 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:16014725 736155 Pak3 p21 (RAC1) activated kinase 3 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20201022 MGI PMID:31943058 736155 Pak3 p21 (RAC1) activated kinase 3 gene MP:0002805 abnormal conditioned taste aversion behavior IAGP N RGD:5509061 20141003 MGI PMID:16014725 736155 Pak3 p21 (RAC1) activated kinase 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20201022 MGI PMID:31943058 736155 Pak3 p21 (RAC1) activated kinase 3 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20201022 MGI PMID:31943058 736155 Pak3 p21 (RAC1) activated kinase 3 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20201022 MGI PMID:31943058 736155 Pak3 p21 (RAC1) activated kinase 3 gene MP:0020335 abnormal dentate gyrus neuron dendrite morphology IAGP N RGD:5509061 20201022 MGI PMID:31943058 736159 Il1rl1 interleukin 1 receptor-like 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10562328 736159 Il1rl1 interleukin 1 receptor-like 1 gene MP:0002465 abnormal eosinophil physiology IAGP N RGD:5509061 20141003 MGI PMID:10727469 736159 Il1rl1 interleukin 1 receptor-like 1 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:20200518 736159 Il1rl1 interleukin 1 receptor-like 1 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:10727469 736159 Il1rl1 interleukin 1 receptor-like 1 gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20141003 MGI PMID:22542450 736159 Il1rl1 interleukin 1 receptor-like 1 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10940882 736159 Il1rl1 interleukin 1 receptor-like 1 gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:20200518 736159 Il1rl1 interleukin 1 receptor-like 1 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:10940882 736159 Il1rl1 interleukin 1 receptor-like 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:20200518 736159 Il1rl1 interleukin 1 receptor-like 1 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:10727469 736159 Il1rl1 interleukin 1 receptor-like 1 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:10727469 736159 Il1rl1 interleukin 1 receptor-like 1 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:10727469 736159 Il1rl1 interleukin 1 receptor-like 1 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:10727469 736159 Il1rl1 interleukin 1 receptor-like 1 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:10940882 736165 Gja5 gap junction protein, alpha 5 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:12435353 736165 Gja5 gap junction protein, alpha 5 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:12842919 736165 Gja5 gap junction protein, alpha 5 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:12842919 736165 Gja5 gap junction protein, alpha 5 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:12842919 736165 Gja5 gap junction protein, alpha 5 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12435353 736165 Gja5 gap junction protein, alpha 5 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:12435353 736165 Gja5 gap junction protein, alpha 5 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:12435353 736165 Gja5 gap junction protein, alpha 5 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12435353 736165 Gja5 gap junction protein, alpha 5 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:9501070 736165 Gja5 gap junction protein, alpha 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20026782 736165 Gja5 gap junction protein, alpha 5 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:20026782 736165 Gja5 gap junction protein, alpha 5 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:9501070 736165 Gja5 gap junction protein, alpha 5 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:12842919 736165 Gja5 gap junction protein, alpha 5 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:14630724 736165 Gja5 gap junction protein, alpha 5 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:21825130 736165 Gja5 gap junction protein, alpha 5 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:9501069 736165 Gja5 gap junction protein, alpha 5 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:9501070 736165 Gja5 gap junction protein, alpha 5 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:9501069 736165 Gja5 gap junction protein, alpha 5 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:9501070 736165 Gja5 gap junction protein, alpha 5 gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:21597036 736165 Gja5 gap junction protein, alpha 5 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:9501069 736165 Gja5 gap junction protein, alpha 5 gene MP:0003898 abnormal QRS complex IAGP N RGD:5509061 20141003 MGI PMID:9501069 736165 Gja5 gap junction protein, alpha 5 gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:14630724 736165 Gja5 gap junction protein, alpha 5 gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:9501069 736165 Gja5 gap junction protein, alpha 5 gene MP:0004071 prolonged P wave IAGP N RGD:5509061 20141003 MGI PMID:9501070 736165 Gja5 gap junction protein, alpha 5 gene MP:0004072 abnormal frontal plane axis IAGP N RGD:5509061 20141003 MGI PMID:9501069 736165 Gja5 gap junction protein, alpha 5 gene MP:0004253 bifid atrial appendage IAGP N RGD:5509061 20141003 MGI PMID:12842919 736165 Gja5 gap junction protein, alpha 5 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21597036 736165 Gja5 gap junction protein, alpha 5 gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:20530546 736165 Gja5 gap junction protein, alpha 5 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:20026782 736165 Gja5 gap junction protein, alpha 5 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:12435353 736165 Gja5 gap junction protein, alpha 5 gene MP:0006122 mitral valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:12842919 736165 Gja5 gap junction protein, alpha 5 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:14630724 736165 Gja5 gap junction protein, alpha 5 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:9501069 736165 Gja5 gap junction protein, alpha 5 gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:9501070 736165 Gja5 gap junction protein, alpha 5 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12842919 736165 Gja5 gap junction protein, alpha 5 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:12842919 736165 Gja5 gap junction protein, alpha 5 gene MP:0010460 pulmonary artery hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12842919 736165 Gja5 gap junction protein, alpha 5 gene MP:0010464 abnormal aortic arch and aortic arch branch attachment IAGP N RGD:5509061 20141003 MGI PMID:12842919 736165 Gja5 gap junction protein, alpha 5 gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:14630724 736165 Gja5 gap junction protein, alpha 5 gene MP:0010514 fragmented QRS complex IAGP N RGD:5509061 20141003 MGI PMID:9501069 736165 Gja5 gap junction protein, alpha 5 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:12842919 736165 Gja5 gap junction protein, alpha 5 gene MP:0010636 bundle branch block IAGP N RGD:5509061 20141003 MGI PMID:9501069 736165 Gja5 gap junction protein, alpha 5 gene MP:0010922 alveolitis IAGP N RGD:5509061 20141003 MGI PMID:20026782 736165 Gja5 gap junction protein, alpha 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12435353 736165 Gja5 gap junction protein, alpha 5 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12435353 736165 Gja5 gap junction protein, alpha 5 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12842919 736165 Gja5 gap junction protein, alpha 5 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12435353 736165 Gja5 gap junction protein, alpha 5 gene MP:0011953 prolonged PQ interval IAGP N RGD:5509061 20141003 MGI PMID:9501070 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0000479 abnormal enterocyte morphology IAGP N RGD:5509061 20200820 MGI PMID:32728212 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20181129 MGI PMID:28878021 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20181129 MGI PMID:28878021 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20181129 MGI PMID:28878021 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20181129 MGI PMID:28878021 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20181129 MGI PMID:28878021 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21331045 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21331045 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0002083 premature death IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0004120 cardiac ischemia IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20181129 MGI PMID:28878021 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21331045 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20181129 MGI PMID:28878021 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20181129 MGI PMID:28878021 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20190314 MGI PMID:30064974 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21331045 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20200820 MGI PMID:32728212 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0009387 abnormal epidermal pigmentation IAGP N RGD:5509061 20181129 MGI PMID:28878021 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20181129 MGI PMID:28878021 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0010158 abnormal intestine development IAGP N RGD:5509061 20200820 MGI PMID:32728212 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0010763 abnormal hematopoietic stem cell physiology IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21331045 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20181129 MGI PMID:28878021 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20181129 MGI PMID:28878021 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0012015 abnormal eumelanosome eumelanin content IAGP N RGD:5509061 20181129 MGI PMID:28878021 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0012022 increased melanocyte number IAGP N RGD:5509061 20181129 MGI PMID:28878021 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0013483 abnormal jejunum crypts of Lieberkuhn morphology IAGP N RGD:5509061 20200820 MGI PMID:32728212 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0013501 increased fibroblast apoptosis IAGP N RGD:5509061 20150212 MGI PMID:21331045 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0013657 abnormal blood cell morphology IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0013659 abnormal erythroid lineage cell morphology IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0013662 decreased myeloid cell number IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0013776 bone marrow failure IAGP N RGD:5509061 20160505 MGI PMID:25242043 736168 Csnk1a1 casein kinase 1, alpha 1 gene MP:0030051 increased foot pigmentation IAGP N RGD:5509061 20181129 MGI PMID:28878021 736171 Capn3 calpain 3 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:11134085 736171 Capn3 calpain 3 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:20592470 736171 Capn3 calpain 3 gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:20855473 736171 Capn3 calpain 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15138196 736171 Capn3 calpain 3 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15138196 736171 Capn3 calpain 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20855473 736171 Capn3 calpain 3 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:15138196 736171 Capn3 calpain 3 gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:20855473 736171 Capn3 calpain 3 gene MP:0003081 abnormal soleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15138196 736171 Capn3 calpain 3 gene MP:0003082 abnormal gastrocnemius morphology IAGP N RGD:5509061 20141003 MGI PMID:15138196 736171 Capn3 calpain 3 gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20141003 MGI PMID:15138196 736171 Capn3 calpain 3 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15138196 736171 Capn3 calpain 3 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20592470 736171 Capn3 calpain 3 gene MP:0004121 abnormal sarcolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:11134085 736171 Capn3 calpain 3 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:11134085 736171 Capn3 calpain 3 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:15138196 736171 Capn3 calpain 3 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:20592470 736171 Capn3 calpain 3 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:20592470 736171 Capn3 calpain 3 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:20855473 736171 Capn3 calpain 3 gene MP:0009415 skeletal muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:20592470 736171 Capn3 calpain 3 gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:20592470 736171 Capn3 calpain 3 gene MP:0030566 abnormal A band morphology IAGP N RGD:5509061 20180531 MGI PMID:15138196 736173 Becn1 beclin 1, autophagy related gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 736173 Becn1 beclin 1, autophagy related gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 736173 Becn1 beclin 1, autophagy related gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:21464117 736173 Becn1 beclin 1, autophagy related gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:21464117 736173 Becn1 beclin 1, autophagy related gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:21464117 736173 Becn1 beclin 1, autophagy related gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:21464117 736173 Becn1 beclin 1, autophagy related gene MP:0001262 decreased body weight IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0001488 increased startle reflex IEA N RGD:5509061 20181227 MGI 736173 Becn1 beclin 1, autophagy related gene MP:0001661 extended life span IAGP N RGD:5509061 20181206 MGI PMID:28806762 736173 Becn1 beclin 1, autophagy related gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:14657337 736173 Becn1 beclin 1, autophagy related gene MP:0001710 absent amniotic folds IAGP N RGD:5509061 20141003 MGI PMID:14657337 736173 Becn1 beclin 1, autophagy related gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:14657337 736173 Becn1 beclin 1, autophagy related gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14657337 736173 Becn1 beclin 1, autophagy related gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14657337 736173 Becn1 beclin 1, autophagy related gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14657337 736173 Becn1 beclin 1, autophagy related gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:21464117 736173 Becn1 beclin 1, autophagy related gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20181206 MGI PMID:28806762 736173 Becn1 beclin 1, autophagy related gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0002493 increased IgG level IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0003037 increased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:21737790 736173 Becn1 beclin 1, autophagy related gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:21737790 736173 Becn1 beclin 1, autophagy related gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20181206 MGI PMID:28806762 736173 Becn1 beclin 1, autophagy related gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14657337 736173 Becn1 beclin 1, autophagy related gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 736173 Becn1 beclin 1, autophagy related gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21660048 736173 Becn1 beclin 1, autophagy related gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20240620 MGI PMID:33355624 736173 Becn1 beclin 1, autophagy related gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:14657337 736173 Becn1 beclin 1, autophagy related gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21660048 736173 Becn1 beclin 1, autophagy related gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 736173 Becn1 beclin 1, autophagy related gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21660048 736173 Becn1 beclin 1, autophagy related gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0006413 increased T cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21660048 736173 Becn1 beclin 1, autophagy related gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21660048 736173 Becn1 beclin 1, autophagy related gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21660048 736173 Becn1 beclin 1, autophagy related gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0008483 increased spleen germinal center size IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0008594 decreased circulating interleukin-10 level IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0008647 increased circulating interleukin-12b level IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0008714 increased lung carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0009317 increased follicular lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0009361 abnormal primordial ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:21464117 736173 Becn1 beclin 1, autophagy related gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 736173 Becn1 beclin 1, autophagy related gene MP:0010209 abnormal circulating chemokine level IAGP N RGD:5509061 20190502 MGI PMID:27096368 736173 Becn1 beclin 1, autophagy related gene MP:0010286 increased plasmacytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14657337 736173 Becn1 beclin 1, autophagy related gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736173 Becn1 beclin 1, autophagy related gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21464117 736173 Becn1 beclin 1, autophagy related gene MP:0011121 decreased primordial ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:21464117 736173 Becn1 beclin 1, autophagy related gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:22258505 736173 Becn1 beclin 1, autophagy related gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:14657337 736173 Becn1 beclin 1, autophagy related gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:14638851 736173 Becn1 beclin 1, autophagy related gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:14657337 736173 Becn1 beclin 1, autophagy related gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:22258505 736173 Becn1 beclin 1, autophagy related gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20190711 MGI PMID:28806762 736175 Camk2d calcium/calmodulin-dependent protein kinase II, delta gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:23426181 736175 Camk2d calcium/calmodulin-dependent protein kinase II, delta gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23426181 736175 Camk2d calcium/calmodulin-dependent protein kinase II, delta gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:23363625 736175 Camk2d calcium/calmodulin-dependent protein kinase II, delta gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:19179290 736175 Camk2d calcium/calmodulin-dependent protein kinase II, delta gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:19381018 736175 Camk2d calcium/calmodulin-dependent protein kinase II, delta gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20240523 MGI PMID:32749237 736175 Camk2d calcium/calmodulin-dependent protein kinase II, delta gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:23426181 736175 Camk2d calcium/calmodulin-dependent protein kinase II, delta gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:23426181 736175 Camk2d calcium/calmodulin-dependent protein kinase II, delta gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23426181 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:10898794 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:10898794 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10898794 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0000858 abnormal metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17936562 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10898794 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:10898794 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10898794 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:10898794 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11711428 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0002021 increased incidence of induced tumors IAGP N RGD:5509061 20141003 MGI PMID:10898794 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17936562 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17936562 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17936562 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:17936562 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10898794 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17936562 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10898794 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17936562 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17936562 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17936562 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:10898794 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:10898794 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:11711428 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:17936562 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0010314 increased neurofibroma incidence IAGP N RGD:5509061 20141003 MGI PMID:17936562 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0010315 increased cholangiocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17936562 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10898794 736178 Dmtf1 cyclin D binding myb like transcription factor 1 gene MP:0013320 dilated seminal vesicle IAGP N RGD:5509061 20141204 MGI PMID:10898794 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:24216512 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:24216512 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0001391 abnormal tail movements IAGP N RGD:5509061 20141003 MGI PMID:22087007 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:24216512 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:22087007 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:22087007 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:22087007 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:21903816 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:15314237 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:17035534 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:19931571 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:15314237 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21903816 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:24216512 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22087007 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:24216512 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:16857712 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20141003 MGI PMID:10448219 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:10448219 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:15314237 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:21295407 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:21903816 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0002822 catalepsy IAGP N RGD:5509061 20141003 MGI PMID:22087007 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:10448219 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0003177 allodynia IAGP N RGD:5509061 20141003 MGI PMID:17035534 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:22087007 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0003469 decreased single cell response intensity IAGP N RGD:5509061 20141003 MGI PMID:17035534 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:22087007 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:24216512 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:22087007 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:16857712 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0005407 hyperalgesia IAGP N RGD:5509061 20141003 MGI PMID:19931571 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:21903816 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21295407 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:24216512 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0009748 abnormal behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:24069332 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0010504 abnormal RR interval IAGP N RGD:5509061 20141003 MGI PMID:22087007 736179 Scn10a sodium channel, voltage-gated, type X, alpha gene MP:0010637 sinus bradycardia IAGP N RGD:5509061 20141003 MGI PMID:22087007 736181 Glul glutamate-ammonia ligase gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20190418 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20190418 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160421 MGI PMID:25870278 736181 Glul glutamate-ammonia ligase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20190418 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:20064933 736181 Glul glutamate-ammonia ligase gene MP:0001765 abnormal ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20064933 736181 Glul glutamate-ammonia ligase gene MP:0002064 seizures IAGP N RGD:5509061 20190418 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0002083 premature death IAGP N RGD:5509061 20160421 MGI PMID:25870278 736181 Glul glutamate-ammonia ligase gene MP:0002083 premature death IAGP N RGD:5509061 20190418 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:20140959 736181 Glul glutamate-ammonia ligase gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25870278 736181 Glul glutamate-ammonia ligase gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20190418 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20190418 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0003106 abnormal fear-related response IAGP N RGD:5509061 20160421 MGI PMID:25870278 736181 Glul glutamate-ammonia ligase gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20190418 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0003354 astrocytosis IAGP N RGD:5509061 20190418 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0003674 oxidative stress IAGP N RGD:5509061 20160421 MGI PMID:25870278 736181 Glul glutamate-ammonia ligase gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20190418 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20160421 MGI PMID:25870278 736181 Glul glutamate-ammonia ligase gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:20064933 736181 Glul glutamate-ammonia ligase gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:20140959 736181 Glul glutamate-ammonia ligase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20140959 736181 Glul glutamate-ammonia ligase gene MP:0010014 hippocampus pyramidal cell degeneration IAGP N RGD:5509061 20190418 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20140959 736181 Glul glutamate-ammonia ligase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17557305 736181 Glul glutamate-ammonia ligase gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17557305 736181 Glul glutamate-ammonia ligase gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17557305 736181 Glul glutamate-ammonia ligase gene MP:0030604 abnormal ammonia homeostasis IAGP N RGD:5509061 20180920 MGI PMID:20064933 736181 Glul glutamate-ammonia ligase gene MP:0030604 abnormal ammonia homeostasis IAGP N RGD:5509061 20180920 MGI PMID:20140959 736181 Glul glutamate-ammonia ligase gene MP:0030658 increased glycine level IAGP N RGD:5509061 20180913 MGI PMID:20140959 736181 Glul glutamate-ammonia ligase gene MP:0030707 decreased glutamine level IAGP N RGD:5509061 20180920 MGI PMID:20064933 736181 Glul glutamate-ammonia ligase gene MP:0030707 decreased glutamine level IAGP N RGD:5509061 20180920 MGI PMID:20140959 736181 Glul glutamate-ammonia ligase gene MP:0030707 decreased glutamine level IAGP N RGD:5509061 20190418 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0030710 decreased circulating glutamine level IAGP N RGD:5509061 20180920 MGI PMID:20064933 736181 Glul glutamate-ammonia ligase gene MP:0030733 decreased gamma-aminobutyric acid level IAGP N RGD:5509061 20190418 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0030737 decreased glutamic acid level IAGP N RGD:5509061 20190418 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0030743 decreased aspartic acid level IAGP N RGD:5509061 20190418 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:30053506 736181 Glul glutamate-ammonia ligase gene MP:0031639 decreased alanine level IAGP N RGD:5509061 20240801 MGI PMID:20140959 736191 Neu2 neuraminidase 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0001261 obese IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0003249 increased muscle free fatty acids level IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0009406 decreased skeletal muscle fiber number IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0010359 increased liver free fatty acids level IAGP N RGD:5509061 20220324 MGI PMID:35217678 736191 Neu2 neuraminidase 2 gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20220324 MGI PMID:35217678 736194 Psmb8 proteasome (prosome, macropain) subunit, beta type 8 (large multifunctional peptidase 7) gene MP:0001836 abnormal antigen presentation via MHC class I IAGP N RGD:5509061 20141003 MGI PMID:22197977 736194 Psmb8 proteasome (prosome, macropain) subunit, beta type 8 (large multifunctional peptidase 7) gene MP:0001838 defective intracellular transport of class I molecules IAGP N RGD:5509061 20141003 MGI PMID:8066463 736194 Psmb8 proteasome (prosome, macropain) subunit, beta type 8 (large multifunctional peptidase 7) gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:22197977 736194 Psmb8 proteasome (prosome, macropain) subunit, beta type 8 (large multifunctional peptidase 7) gene MP:0001841 decreased level of surface class I molecules IAGP N RGD:5509061 20141003 MGI PMID:8066463 736194 Psmb8 proteasome (prosome, macropain) subunit, beta type 8 (large multifunctional peptidase 7) gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:16569681 736194 Psmb8 proteasome (prosome, macropain) subunit, beta type 8 (large multifunctional peptidase 7) gene MP:0002453 abnormal B lymphocyte antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:22197977 736194 Psmb8 proteasome (prosome, macropain) subunit, beta type 8 (large multifunctional peptidase 7) gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:22197977 736194 Psmb8 proteasome (prosome, macropain) subunit, beta type 8 (large multifunctional peptidase 7) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16549793 736194 Psmb8 proteasome (prosome, macropain) subunit, beta type 8 (large multifunctional peptidase 7) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22197977 736194 Psmb8 proteasome (prosome, macropain) subunit, beta type 8 (large multifunctional peptidase 7) gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23569244 736194 Psmb8 proteasome (prosome, macropain) subunit, beta type 8 (large multifunctional peptidase 7) gene MP:0008754 abnormal T cell receptor V(D)J recombination IAGP N RGD:5509061 20141003 MGI PMID:23569244 736196 Pcolce procollagen C-endopeptidase enhancer protein gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16354695 736196 Pcolce procollagen C-endopeptidase enhancer protein gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:16354695 736196 Pcolce procollagen C-endopeptidase enhancer protein gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:16354695 736196 Pcolce procollagen C-endopeptidase enhancer protein gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20200310 MGI PMID:28746876 736196 Pcolce procollagen C-endopeptidase enhancer protein gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16354695 736196 Pcolce procollagen C-endopeptidase enhancer protein gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16354695 736196 Pcolce procollagen C-endopeptidase enhancer protein gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16354695 736196 Pcolce procollagen C-endopeptidase enhancer protein gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:16354695 736196 Pcolce procollagen C-endopeptidase enhancer protein gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20200310 MGI PMID:28746876 736196 Pcolce procollagen C-endopeptidase enhancer protein gene MP:0005503 abnormal tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:16354695 736196 Pcolce procollagen C-endopeptidase enhancer protein gene MP:0010967 increased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:16354695 736196 Pcolce procollagen C-endopeptidase enhancer protein gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20230706 MGI PMID:28746876 736198 Dnase1 deoxyribonuclease I gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 736198 Dnase1 deoxyribonuclease I gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 736198 Dnase1 deoxyribonuclease I gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 736198 Dnase1 deoxyribonuclease I gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10835632 736198 Dnase1 deoxyribonuclease I gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 736198 Dnase1 deoxyribonuclease I gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:10835632 736198 Dnase1 deoxyribonuclease I gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10835632 736198 Dnase1 deoxyribonuclease I gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20200402 MGI PMID:30758851 736198 Dnase1 deoxyribonuclease I gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:10835632 736198 Dnase1 deoxyribonuclease I gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20200402 MGI PMID:30758851 736198 Dnase1 deoxyribonuclease I gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:15647342 736198 Dnase1 deoxyribonuclease I gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20200402 MGI PMID:30758851 736198 Dnase1 deoxyribonuclease I gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:15647342 736198 Dnase1 deoxyribonuclease I gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 736198 Dnase1 deoxyribonuclease I gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20200402 MGI PMID:30758851 736198 Dnase1 deoxyribonuclease I gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:10835632 736198 Dnase1 deoxyribonuclease I gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20200402 MGI PMID:30758851 736198 Dnase1 deoxyribonuclease I gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20200402 MGI PMID:30758851 736198 Dnase1 deoxyribonuclease I gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:10835632 736198 Dnase1 deoxyribonuclease I gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20200402 MGI PMID:30758851 736198 Dnase1 deoxyribonuclease I gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:15647342 736198 Dnase1 deoxyribonuclease I gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20200402 MGI PMID:30758851 736198 Dnase1 deoxyribonuclease I gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:15647342 736198 Dnase1 deoxyribonuclease I gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:15647342 736198 Dnase1 deoxyribonuclease I gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 736198 Dnase1 deoxyribonuclease I gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15647342 736198 Dnase1 deoxyribonuclease I gene MP:0011371 decreased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15647342 736200 Csnk1g1 casein kinase 1, gamma 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20220811 MGI 736200 Csnk1g1 casein kinase 1, gamma 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 736200 Csnk1g1 casein kinase 1, gamma 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 736200 Csnk1g1 casein kinase 1, gamma 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 736200 Csnk1g1 casein kinase 1, gamma 1 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 736200 Csnk1g1 casein kinase 1, gamma 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20231207 MGI 736201 Stmn1 stathmin 1 gene MP:0000751 myopathy IAGP N RGD:5509061 20141003 MGI PMID:11839567 736201 Stmn1 stathmin 1 gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:11839567 736201 Stmn1 stathmin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8662897 736201 Stmn1 stathmin 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:11839567 736201 Stmn1 stathmin 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:11839567 736201 Stmn1 stathmin 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:19033656 736201 Stmn1 stathmin 1 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:11839567 736201 Stmn1 stathmin 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:11839567 736201 Stmn1 stathmin 1 gene MP:0021002 brain lesion IAGP N RGD:5509061 20210805 MGI PMID:11839567 736203 Sema6b sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6B gene MP:0002761 abnormal hippocampal mossy fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:20484647 736205 Irs2 insulin receptor substrate 2 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18590693 736205 Irs2 insulin receptor substrate 2 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18590693 736205 Irs2 insulin receptor substrate 2 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:11812758 736205 Irs2 insulin receptor substrate 2 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18288891 736205 Irs2 insulin receptor substrate 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:17329594 736205 Irs2 insulin receptor substrate 2 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:17329594 736205 Irs2 insulin receptor substrate 2 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:17329594 736205 Irs2 insulin receptor substrate 2 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:15467829 736205 Irs2 insulin receptor substrate 2 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:15841180 736205 Irs2 insulin receptor substrate 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15467829 736205 Irs2 insulin receptor substrate 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15467830 736205 Irs2 insulin receptor substrate 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15841180 736205 Irs2 insulin receptor substrate 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20160204 MGI PMID:24567904 736205 Irs2 insulin receptor substrate 2 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:15467830 736205 Irs2 insulin receptor substrate 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11812758 736205 Irs2 insulin receptor substrate 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14693698 736205 Irs2 insulin receptor substrate 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15467829 736205 Irs2 insulin receptor substrate 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9495343 736205 Irs2 insulin receptor substrate 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18288891 736205 Irs2 insulin receptor substrate 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18590693 736205 Irs2 insulin receptor substrate 2 gene MP:0001377 abnormal mating frequency IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:15467829 736205 Irs2 insulin receptor substrate 2 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:9495343 736205 Irs2 insulin receptor substrate 2 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:15467829 736205 Irs2 insulin receptor substrate 2 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:15841180 736205 Irs2 insulin receptor substrate 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12810606 736205 Irs2 insulin receptor substrate 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15467830 736205 Irs2 insulin receptor substrate 2 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12810606 736205 Irs2 insulin receptor substrate 2 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12810606 736205 Irs2 insulin receptor substrate 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12810606 736205 Irs2 insulin receptor substrate 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:14617753 736205 Irs2 insulin receptor substrate 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:14693698 736205 Irs2 insulin receptor substrate 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15467829 736205 Irs2 insulin receptor substrate 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:15685168 736205 Irs2 insulin receptor substrate 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:18288891 736205 Irs2 insulin receptor substrate 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:18590693 736205 Irs2 insulin receptor substrate 2 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:9495343 736205 Irs2 insulin receptor substrate 2 gene MP:0001560 abnormal circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14617753 736205 Irs2 insulin receptor substrate 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:9495343 736205 Irs2 insulin receptor substrate 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11259600 736205 Irs2 insulin receptor substrate 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15467829 736205 Irs2 insulin receptor substrate 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11812758 736205 Irs2 insulin receptor substrate 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12488434 736205 Irs2 insulin receptor substrate 2 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20160204 MGI PMID:24567904 736205 Irs2 insulin receptor substrate 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11078455 736205 Irs2 insulin receptor substrate 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14617753 736205 Irs2 insulin receptor substrate 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15467829 736205 Irs2 insulin receptor substrate 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15685168 736205 Irs2 insulin receptor substrate 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15841180 736205 Irs2 insulin receptor substrate 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18288891 736205 Irs2 insulin receptor substrate 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18590692 736205 Irs2 insulin receptor substrate 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18590693 736205 Irs2 insulin receptor substrate 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20074531 736205 Irs2 insulin receptor substrate 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9495343 736205 Irs2 insulin receptor substrate 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20160204 MGI PMID:24567904 736205 Irs2 insulin receptor substrate 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12488434 736205 Irs2 insulin receptor substrate 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14617753 736205 Irs2 insulin receptor substrate 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:14693698 736205 Irs2 insulin receptor substrate 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9495343 736205 Irs2 insulin receptor substrate 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15685168 736205 Irs2 insulin receptor substrate 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15841180 736205 Irs2 insulin receptor substrate 2 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20160204 MGI PMID:24567904 736205 Irs2 insulin receptor substrate 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18590693 736205 Irs2 insulin receptor substrate 2 gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:17329594 736205 Irs2 insulin receptor substrate 2 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18590693 736205 Irs2 insulin receptor substrate 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15467829 736205 Irs2 insulin receptor substrate 2 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:14693698 736205 Irs2 insulin receptor substrate 2 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:11078455 736205 Irs2 insulin receptor substrate 2 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:14617753 736205 Irs2 insulin receptor substrate 2 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:15841180 736205 Irs2 insulin receptor substrate 2 gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:15685168 736205 Irs2 insulin receptor substrate 2 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20200123 MGI PMID:15689562 736205 Irs2 insulin receptor substrate 2 gene MP:0003970 abnormal prolactin level IAGP N RGD:5509061 20141003 MGI PMID:17329594 736205 Irs2 insulin receptor substrate 2 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200123 MGI PMID:15689562 736205 Irs2 insulin receptor substrate 2 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200123 MGI PMID:15689562 736205 Irs2 insulin receptor substrate 2 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:18590692 736205 Irs2 insulin receptor substrate 2 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:18590693 736205 Irs2 insulin receptor substrate 2 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:12810606 736205 Irs2 insulin receptor substrate 2 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:11259600 736205 Irs2 insulin receptor substrate 2 gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12810606 736205 Irs2 insulin receptor substrate 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15467830 736205 Irs2 insulin receptor substrate 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18590693 736205 Irs2 insulin receptor substrate 2 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11078455 736205 Irs2 insulin receptor substrate 2 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14617753 736205 Irs2 insulin receptor substrate 2 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14693698 736205 Irs2 insulin receptor substrate 2 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15467829 736205 Irs2 insulin receptor substrate 2 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15685168 736205 Irs2 insulin receptor substrate 2 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20160204 MGI PMID:24567904 736205 Irs2 insulin receptor substrate 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11078455 736205 Irs2 insulin receptor substrate 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:14693698 736205 Irs2 insulin receptor substrate 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15467829 736205 Irs2 insulin receptor substrate 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15467830 736205 Irs2 insulin receptor substrate 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15841180 736205 Irs2 insulin receptor substrate 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18590693 736205 Irs2 insulin receptor substrate 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20074531 736205 Irs2 insulin receptor substrate 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:9495343 736205 Irs2 insulin receptor substrate 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20160204 MGI PMID:24567904 736205 Irs2 insulin receptor substrate 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11078455 736205 Irs2 insulin receptor substrate 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12810606 736205 Irs2 insulin receptor substrate 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15467829 736205 Irs2 insulin receptor substrate 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:15467830 736205 Irs2 insulin receptor substrate 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:18288891 736205 Irs2 insulin receptor substrate 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:18590692 736205 Irs2 insulin receptor substrate 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:18590693 736205 Irs2 insulin receptor substrate 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:20074531 736205 Irs2 insulin receptor substrate 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:9495343 736205 Irs2 insulin receptor substrate 2 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20160204 MGI PMID:24567904 736205 Irs2 insulin receptor substrate 2 gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0005448 abnormal energy homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20160204 MGI PMID:24567904 736205 Irs2 insulin receptor substrate 2 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:14693698 736205 Irs2 insulin receptor substrate 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15467829 736205 Irs2 insulin receptor substrate 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15467830 736205 Irs2 insulin receptor substrate 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15685168 736205 Irs2 insulin receptor substrate 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15841180 736205 Irs2 insulin receptor substrate 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18288891 736205 Irs2 insulin receptor substrate 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18590693 736205 Irs2 insulin receptor substrate 2 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20160204 MGI PMID:24567904 736205 Irs2 insulin receptor substrate 2 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:12810606 736205 Irs2 insulin receptor substrate 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15467829 736205 Irs2 insulin receptor substrate 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15467830 736205 Irs2 insulin receptor substrate 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:15841180 736205 Irs2 insulin receptor substrate 2 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20160204 MGI PMID:24567904 736205 Irs2 insulin receptor substrate 2 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20200123 MGI PMID:15689562 736205 Irs2 insulin receptor substrate 2 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12810606 736205 Irs2 insulin receptor substrate 2 gene MP:0008335 decreased gonadotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0008368 small pituitary intermediate lobe IAGP N RGD:5509061 20141003 MGI PMID:11812758 736205 Irs2 insulin receptor substrate 2 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200123 MGI PMID:15689562 736205 Irs2 insulin receptor substrate 2 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20200123 MGI PMID:15689562 736205 Irs2 insulin receptor substrate 2 gene MP:0008582 short photoreceptor inner segment IAGP N RGD:5509061 20200123 MGI PMID:15689562 736205 Irs2 insulin receptor substrate 2 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200123 MGI PMID:15689562 736205 Irs2 insulin receptor substrate 2 gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:17329594 736205 Irs2 insulin receptor substrate 2 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20141003 MGI PMID:17329594 736205 Irs2 insulin receptor substrate 2 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20180614 MGI PMID:15841180 736205 Irs2 insulin receptor substrate 2 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:11078455 736205 Irs2 insulin receptor substrate 2 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:18288891 736205 Irs2 insulin receptor substrate 2 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:9495343 736205 Irs2 insulin receptor substrate 2 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20180614 MGI PMID:15467830 736205 Irs2 insulin receptor substrate 2 gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20160204 MGI PMID:24567904 736205 Irs2 insulin receptor substrate 2 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:15685168 736205 Irs2 insulin receptor substrate 2 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:15685168 736205 Irs2 insulin receptor substrate 2 gene MP:0009174 absent pancreatic beta cells IAGP N RGD:5509061 20180614 MGI PMID:12488434 736205 Irs2 insulin receptor substrate 2 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20180614 MGI PMID:15467830 736205 Irs2 insulin receptor substrate 2 gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20141003 MGI PMID:17329594 736205 Irs2 insulin receptor substrate 2 gene MP:0009488 abnormal pancreatic islet cell apoptosis IAGP N RGD:5509061 20180614 MGI PMID:18288891 736205 Irs2 insulin receptor substrate 2 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:9495343 736205 Irs2 insulin receptor substrate 2 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15467829 736205 Irs2 insulin receptor substrate 2 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:15841180 736205 Irs2 insulin receptor substrate 2 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:18590693 736205 Irs2 insulin receptor substrate 2 gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20191226 MGI PMID:11812758 736205 Irs2 insulin receptor substrate 2 gene MP:0011125 decreased primary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:11014193 736205 Irs2 insulin receptor substrate 2 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:17329594 736205 Irs2 insulin receptor substrate 2 gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20180614 MGI PMID:18288891 736205 Irs2 insulin receptor substrate 2 gene MP:0011939 increased food intake IAGP N RGD:5509061 20160204 MGI PMID:24567904 736205 Irs2 insulin receptor substrate 2 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200123 MGI PMID:15689562 736205 Irs2 insulin receptor substrate 2 gene MP:0012039 abnormal b-wave implicit time IAGP N RGD:5509061 20200123 MGI PMID:15689562 736205 Irs2 insulin receptor substrate 2 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20200123 MGI PMID:15689562 736205 Irs2 insulin receptor substrate 2 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20200123 MGI PMID:15689562 736205 Irs2 insulin receptor substrate 2 gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20160204 MGI PMID:24567904 736205 Irs2 insulin receptor substrate 2 gene MP:0014441 decreased response to leptin IAGP N RGD:5509061 20240523 MGI PMID:15467830 736205 Irs2 insulin receptor substrate 2 gene MP:0020234 decreased basal metabolism IAGP N RGD:5509061 20160204 MGI PMID:24567904 736205 Irs2 insulin receptor substrate 2 gene MP:0031018 decreased granulosa cell proliferation IAGP N RGD:5509061 20220407 MGI PMID:17329594 736205 Irs2 insulin receptor substrate 2 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:17329594 736205 Irs2 insulin receptor substrate 2 gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220804 MGI PMID:11014193 736206 Macroh2a1 macroH2A.1 histone gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20210812 MGI PMID:31439048 736206 Macroh2a1 macroH2A.1 histone gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20210812 MGI PMID:31439048 736206 Macroh2a1 macroH2A.1 histone gene MP:0001258 decreased body length IAGP N RGD:5509061 20180322 MGI PMID:25312643 736206 Macroh2a1 macroH2A.1 histone gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180322 MGI PMID:25312643 736206 Macroh2a1 macroH2A.1 histone gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20180322 MGI PMID:25312643 736206 Macroh2a1 macroH2A.1 histone gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17242180 736206 Macroh2a1 macroH2A.1 histone gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20210812 MGI PMID:31439048 736206 Macroh2a1 macroH2A.1 histone gene MP:0003671 abnormal eyelid aperture IAGP N RGD:5509061 20180322 MGI PMID:25312643 736206 Macroh2a1 macroH2A.1 histone gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20180322 MGI PMID:25312643 736206 Macroh2a1 macroH2A.1 histone gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20180322 MGI PMID:25312643 736206 Macroh2a1 macroH2A.1 histone gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20210812 MGI PMID:31439048 736206 Macroh2a1 macroH2A.1 histone gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20210812 MGI PMID:31439048 736206 Macroh2a1 macroH2A.1 histone gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20210812 MGI PMID:31439048 736206 Macroh2a1 macroH2A.1 histone gene MP:0005251 blepharitis IAGP N RGD:5509061 20180322 MGI PMID:25312643 736206 Macroh2a1 macroH2A.1 histone gene MP:0005409 darkened coat color IAGP N RGD:5509061 20180322 MGI PMID:25312643 736206 Macroh2a1 macroH2A.1 histone gene MP:0005632 decreased circulating aspartate transaminase level IAGP N RGD:5509061 20210812 MGI PMID:31439048 736206 Macroh2a1 macroH2A.1 histone gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20210812 MGI PMID:31439048 736206 Macroh2a1 macroH2A.1 histone gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20180322 MGI PMID:25312643 736206 Macroh2a1 macroH2A.1 histone gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20180322 MGI PMID:25312643 736206 Macroh2a1 macroH2A.1 histone gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20210812 MGI PMID:31439048 736206 Macroh2a1 macroH2A.1 histone gene MP:0013745 abnormal eyelid margin morphology IAGP N RGD:5509061 20180322 MGI PMID:25312643 736206 Macroh2a1 macroH2A.1 histone gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:20359320 736207 Resp18 regulated endocrine-specific protein 18 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230601 MGI 736207 Resp18 regulated endocrine-specific protein 18 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20220519 MGI 736207 Resp18 regulated endocrine-specific protein 18 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20220519 MGI 736207 Resp18 regulated endocrine-specific protein 18 gene MP:0002833 increased heart weight IEA N RGD:5509061 20220811 MGI 736207 Resp18 regulated endocrine-specific protein 18 gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220519 MGI 736207 Resp18 regulated endocrine-specific protein 18 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21104147 736210 Meox2 mesenchyme homeobox 2 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18378898 736210 Meox2 mesenchyme homeobox 2 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:14769860 736210 Meox2 mesenchyme homeobox 2 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:15229648 736210 Meox2 mesenchyme homeobox 2 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:14769860 736210 Meox2 mesenchyme homeobox 2 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0000138 absent vertebrae IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0000151 absent ribs IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18079970 736210 Meox2 mesenchyme homeobox 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:19251646 736210 Meox2 mesenchyme homeobox 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:16801545 736210 Meox2 mesenchyme homeobox 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18079970 736210 Meox2 mesenchyme homeobox 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:19251646 736210 Meox2 mesenchyme homeobox 2 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:19411629 736210 Meox2 mesenchyme homeobox 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:15037549 736210 Meox2 mesenchyme homeobox 2 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:15198985 736210 Meox2 mesenchyme homeobox 2 gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15198985 736210 Meox2 mesenchyme homeobox 2 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:18378898 736210 Meox2 mesenchyme homeobox 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:18378898 736210 Meox2 mesenchyme homeobox 2 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:15037550 736210 Meox2 mesenchyme homeobox 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:18378898 736210 Meox2 mesenchyme homeobox 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0000601 small liver IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20150521 MGI PMID:25574476 736210 Meox2 mesenchyme homeobox 2 gene MP:0000630 mammary gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16007139 736210 Meox2 mesenchyme homeobox 2 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:20862291 736210 Meox2 mesenchyme homeobox 2 gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:10403250 736210 Meox2 mesenchyme homeobox 2 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:10403250 736210 Meox2 mesenchyme homeobox 2 gene MP:0000737 abnormal myotome development IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20150521 MGI PMID:25574476 736210 Meox2 mesenchyme homeobox 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:15653949 736210 Meox2 mesenchyme homeobox 2 gene MP:0000786 abnormal embryonic neuroepithelial layer differentiation IAGP N RGD:5509061 20141003 MGI PMID:15037549 736210 Meox2 mesenchyme homeobox 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15037549 736210 Meox2 mesenchyme homeobox 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20150521 MGI PMID:25574476 736210 Meox2 mesenchyme homeobox 2 gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:15037549 736210 Meox2 mesenchyme homeobox 2 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:17693261 736210 Meox2 mesenchyme homeobox 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16801545 736210 Meox2 mesenchyme homeobox 2 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0000963 fused dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:18378898 736210 Meox2 mesenchyme homeobox 2 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22721776 736210 Meox2 mesenchyme homeobox 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16054062 736210 Meox2 mesenchyme homeobox 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17693261 736210 Meox2 mesenchyme homeobox 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18378898 736210 Meox2 mesenchyme homeobox 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220616 MGI PMID:34343497 736210 Meox2 mesenchyme homeobox 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20150521 MGI PMID:25574476 736210 Meox2 mesenchyme homeobox 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10403250 736210 Meox2 mesenchyme homeobox 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:10403250 736210 Meox2 mesenchyme homeobox 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:17693261 736210 Meox2 mesenchyme homeobox 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:17693261 736210 Meox2 mesenchyme homeobox 2 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:14769860 736210 Meox2 mesenchyme homeobox 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16054062 736210 Meox2 mesenchyme homeobox 2 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:21094155 736210 Meox2 mesenchyme homeobox 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17977525 736210 Meox2 mesenchyme homeobox 2 gene MP:0001705 abnormal proximal-distal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15302604 736210 Meox2 mesenchyme homeobox 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:20862291 736210 Meox2 mesenchyme homeobox 2 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:19464366 736210 Meox2 mesenchyme homeobox 2 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:15302604 736210 Meox2 mesenchyme homeobox 2 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:17977525 736210 Meox2 mesenchyme homeobox 2 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:19464366 736210 Meox2 mesenchyme homeobox 2 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:16801545 736210 Meox2 mesenchyme homeobox 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16432225 736210 Meox2 mesenchyme homeobox 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21664579 736210 Meox2 mesenchyme homeobox 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22721776 736210 Meox2 mesenchyme homeobox 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20150521 MGI PMID:25574476 736210 Meox2 mesenchyme homeobox 2 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19411629 736210 Meox2 mesenchyme homeobox 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:20862291 736210 Meox2 mesenchyme homeobox 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:15037549 736210 Meox2 mesenchyme homeobox 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:18378898 736210 Meox2 mesenchyme homeobox 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19411629 736210 Meox2 mesenchyme homeobox 2 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15037549 736210 Meox2 mesenchyme homeobox 2 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:18378898 736210 Meox2 mesenchyme homeobox 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:20862291 736210 Meox2 mesenchyme homeobox 2 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20862291 736210 Meox2 mesenchyme homeobox 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0002083 premature death IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:15302604 736210 Meox2 mesenchyme homeobox 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17211872 736210 Meox2 mesenchyme homeobox 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20150212 MGI PMID:19633665 736210 Meox2 mesenchyme homeobox 2 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:10403250 736210 Meox2 mesenchyme homeobox 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:14769860 736210 Meox2 mesenchyme homeobox 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:20798259 736210 Meox2 mesenchyme homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17693261 736210 Meox2 mesenchyme homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17913785 736210 Meox2 mesenchyme homeobox 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21664579 736210 Meox2 mesenchyme homeobox 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20150521 MGI PMID:25574476 736210 Meox2 mesenchyme homeobox 2 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0002231 abnormal primitive streak morphology IAGP N RGD:5509061 20141003 MGI PMID:16801545 736210 Meox2 mesenchyme homeobox 2 gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:15956290 736210 Meox2 mesenchyme homeobox 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16054062 736210 Meox2 mesenchyme homeobox 2 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:16054062 736210 Meox2 mesenchyme homeobox 2 gene MP:0002632 vestigial tail IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:16054062 736210 Meox2 mesenchyme homeobox 2 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:16054062 736210 Meox2 mesenchyme homeobox 2 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:16054062 736210 Meox2 mesenchyme homeobox 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:19251646 736210 Meox2 mesenchyme homeobox 2 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:14769860 736210 Meox2 mesenchyme homeobox 2 gene MP:0002766 situs inversus IAGP N RGD:5509061 20141003 MGI PMID:20862291 736210 Meox2 mesenchyme homeobox 2 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:20798259 736210 Meox2 mesenchyme homeobox 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:16054062 736210 Meox2 mesenchyme homeobox 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11927540 736210 Meox2 mesenchyme homeobox 2 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:18378898 736210 Meox2 mesenchyme homeobox 2 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0003082 abnormal gastrocnemius morphology IEA N RGD:5509061 20111116 MGI 736210 Meox2 mesenchyme homeobox 2 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:15956290 736210 Meox2 mesenchyme homeobox 2 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:20862291 736210 Meox2 mesenchyme homeobox 2 gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0003335 exocrine pancreatic insufficiency IAGP N RGD:5509061 20150521 MGI PMID:25574476 736210 Meox2 mesenchyme homeobox 2 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:20862291 736210 Meox2 mesenchyme homeobox 2 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0003358 abnormal hypaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:18378898 736210 Meox2 mesenchyme homeobox 2 gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:20862291 736210 Meox2 mesenchyme homeobox 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:16054062 736210 Meox2 mesenchyme homeobox 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0003717 pallor IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0003787 abnormal imprinting IAGP N RGD:5509061 20141003 MGI PMID:22721776 736210 Meox2 mesenchyme homeobox 2 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:19164512 736210 Meox2 mesenchyme homeobox 2 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0003891 increased allantois apoptosis IAGP N RGD:5509061 20150212 MGI PMID:16801545 736210 Meox2 mesenchyme homeobox 2 gene MP:0003958 heart valve hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19251646 736210 Meox2 mesenchyme homeobox 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16801545 736210 Meox2 mesenchyme homeobox 2 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:15229648 736210 Meox2 mesenchyme homeobox 2 gene MP:0004020 polyhydramnios IAGP N RGD:5509061 20141003 MGI PMID:20862291 736210 Meox2 mesenchyme homeobox 2 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:15037549 736210 Meox2 mesenchyme homeobox 2 gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20150521 MGI PMID:25574476 736210 Meox2 mesenchyme homeobox 2 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:16801545 736210 Meox2 mesenchyme homeobox 2 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0004206 abnormal dermomyotome development IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:22266795 736210 Meox2 mesenchyme homeobox 2 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0004230 abnormal embryonic erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0004248 abnormal epaxial muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:16801545 736210 Meox2 mesenchyme homeobox 2 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15037549 736210 Meox2 mesenchyme homeobox 2 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:10403250 736210 Meox2 mesenchyme homeobox 2 gene MP:0004619 caudal vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0004653 absent caudal vertebrae IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11927540 736210 Meox2 mesenchyme homeobox 2 gene MP:0004760 increased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:10403250 736210 Meox2 mesenchyme homeobox 2 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:15037549 736210 Meox2 mesenchyme homeobox 2 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15037549 736210 Meox2 mesenchyme homeobox 2 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:15037549 736210 Meox2 mesenchyme homeobox 2 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:14769860 736210 Meox2 mesenchyme homeobox 2 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:14769860 736210 Meox2 mesenchyme homeobox 2 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:14769860 736210 Meox2 mesenchyme homeobox 2 gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:14769860 736210 Meox2 mesenchyme homeobox 2 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:15229648 736210 Meox2 mesenchyme homeobox 2 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18079970 736210 Meox2 mesenchyme homeobox 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20150521 MGI PMID:25574476 736210 Meox2 mesenchyme homeobox 2 gene MP:0005155 herniated intestine IAGP N RGD:5509061 20141003 MGI PMID:18378898 736210 Meox2 mesenchyme homeobox 2 gene MP:0005222 abnormal somite size IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0005223 abnormal dorsal-ventral polarity of the somites IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20141003 MGI PMID:18079970 736210 Meox2 mesenchyme homeobox 2 gene MP:0005421 loose skin IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:14769860 736210 Meox2 mesenchyme homeobox 2 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:16054062 736210 Meox2 mesenchyme homeobox 2 gene MP:0006029 abnormal sclerotome morphology IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0006107 abnormal fetal atrioventricular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:16801545 736210 Meox2 mesenchyme homeobox 2 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:16801545 736210 Meox2 mesenchyme homeobox 2 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0006322 abnormal perichondrium morphology IAGP N RGD:5509061 20141003 MGI PMID:15037550 736210 Meox2 mesenchyme homeobox 2 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20141003 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:18378898 736210 Meox2 mesenchyme homeobox 2 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:18378898 736210 Meox2 mesenchyme homeobox 2 gene MP:0008257 thin myometrium IEA N RGD:5509061 20111116 MGI 736210 Meox2 mesenchyme homeobox 2 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:14769860 736210 Meox2 mesenchyme homeobox 2 gene MP:0008393 absent primordial germ cells IAGP N RGD:5509061 20141003 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:14769860 736210 Meox2 mesenchyme homeobox 2 gene MP:0008738 abnormal liver iron level IAGP N RGD:5509061 20141003 MGI PMID:16054062 736210 Meox2 mesenchyme homeobox 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:10403250 736210 Meox2 mesenchyme homeobox 2 gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:16054062 736210 Meox2 mesenchyme homeobox 2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:15037549 736210 Meox2 mesenchyme homeobox 2 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20150521 MGI PMID:25574476 736210 Meox2 mesenchyme homeobox 2 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:15198985 736210 Meox2 mesenchyme homeobox 2 gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:10403250 736210 Meox2 mesenchyme homeobox 2 gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:10403250 736210 Meox2 mesenchyme homeobox 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:10403250 736210 Meox2 mesenchyme homeobox 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15037549 736210 Meox2 mesenchyme homeobox 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20150806 MGI PMID:25324524 736210 Meox2 mesenchyme homeobox 2 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:20798259 736210 Meox2 mesenchyme homeobox 2 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16007139 736210 Meox2 mesenchyme homeobox 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19251646 736210 Meox2 mesenchyme homeobox 2 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:19251646 736210 Meox2 mesenchyme homeobox 2 gene MP:0010466 vascular ring IAGP N RGD:5509061 20141003 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0010588 conotruncal ridge hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:21791606 736210 Meox2 mesenchyme homeobox 2 gene MP:0010779 abnormal stomach muscularis externa morphology IAGP N RGD:5509061 20141003 MGI PMID:15198985 736210 Meox2 mesenchyme homeobox 2 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0011032 impaired branching involved in terminal bronchiole morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16432225 736210 Meox2 mesenchyme homeobox 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17693261 736210 Meox2 mesenchyme homeobox 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21664579 736210 Meox2 mesenchyme homeobox 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20150521 MGI PMID:25574476 736210 Meox2 mesenchyme homeobox 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10403250 736210 Meox2 mesenchyme homeobox 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15037550 736210 Meox2 mesenchyme homeobox 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20798259 736210 Meox2 mesenchyme homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15037549 736210 Meox2 mesenchyme homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17448993 736210 Meox2 mesenchyme homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17693261 736210 Meox2 mesenchyme homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18378898 736210 Meox2 mesenchyme homeobox 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20862291 736210 Meox2 mesenchyme homeobox 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17693261 736210 Meox2 mesenchyme homeobox 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20798259 736210 Meox2 mesenchyme homeobox 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15198985 736210 Meox2 mesenchyme homeobox 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15956290 736210 Meox2 mesenchyme homeobox 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16432225 736210 Meox2 mesenchyme homeobox 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17977525 736210 Meox2 mesenchyme homeobox 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19411629 736210 Meox2 mesenchyme homeobox 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21586752 736210 Meox2 mesenchyme homeobox 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17211872 736210 Meox2 mesenchyme homeobox 2 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17977525 736210 Meox2 mesenchyme homeobox 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16801545 736210 Meox2 mesenchyme homeobox 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17178906 736210 Meox2 mesenchyme homeobox 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19633665 736210 Meox2 mesenchyme homeobox 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20170518 MGI PMID:24876386 736210 Meox2 mesenchyme homeobox 2 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20231109 MGI PMID:36400788 736210 Meox2 mesenchyme homeobox 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17369402 736210 Meox2 mesenchyme homeobox 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16962829 736210 Meox2 mesenchyme homeobox 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20862291 736210 Meox2 mesenchyme homeobox 2 gene MP:0011227 abnormal vitamin B12 level IAGP N RGD:5509061 20141003 MGI PMID:20798259 736210 Meox2 mesenchyme homeobox 2 gene MP:0011246 abnormal fetal liver hematopoietic progenitor cell morphology IAGP N RGD:5509061 20231109 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20220616 MGI PMID:34343497 736210 Meox2 mesenchyme homeobox 2 gene MP:0011411 abnormal gonadal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:15302604 736210 Meox2 mesenchyme homeobox 2 gene MP:0012330 decreased circulating fibrinogen level IAGP N RGD:5509061 20200618 MGI PMID:15956290 736210 Meox2 mesenchyme homeobox 2 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:15037549 736210 Meox2 mesenchyme homeobox 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:19633665 736210 Meox2 mesenchyme homeobox 2 gene MP:0014185 cerebellum atrophy IAGP N RGD:5509061 20161013 MGI PMID:25574476 736210 Meox2 mesenchyme homeobox 2 gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:18519639 736210 Meox2 mesenchyme homeobox 2 gene MP:0014518 myocardial hypertrabeculation IAGP N RGD:5509061 20240822 MGI PMID:33681212 736210 Meox2 mesenchyme homeobox 2 gene MP:0020369 increased intestinal iron level IAGP N RGD:5509061 20161020 MGI PMID:16054062 736210 Meox2 mesenchyme homeobox 2 gene MP:0030286 occipital bone hypoplasia IAGP N RGD:5509061 20171102 MGI PMID:12925591 736210 Meox2 mesenchyme homeobox 2 gene MP:0030798 joint contracture IEA N RGD:5509061 20181011 MGI 736210 Meox2 mesenchyme homeobox 2 gene MP:0030934 decreased primordial germ cell proliferation IAGP N RGD:5509061 20190411 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:18232736 736210 Meox2 mesenchyme homeobox 2 gene MP:0031059 increased circulating C-reactive protein level IAGP N RGD:5509061 20200618 MGI PMID:15956290 736210 Meox2 mesenchyme homeobox 2 gene MP:0031555 abnormal pulmonary valve development IAGP N RGD:5509061 20240125 MGI PMID:33681212 736211 Arl4a ADP-ribosylation factor-like 4A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11909968 736211 Arl4a ADP-ribosylation factor-like 4A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11909968 736211 Arl4a ADP-ribosylation factor-like 4A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:11909968 736211 Arl4a ADP-ribosylation factor-like 4A gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:11909968 736212 Cdh10 cadherin 10 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20231207 MGI 736212 Cdh10 cadherin 10 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 736212 Cdh10 cadherin 10 gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20231207 MGI 736212 Cdh10 cadherin 10 gene MP:0001297 microphthalmia IEA N RGD:5509061 20181227 MGI 736212 Cdh10 cadherin 10 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 736212 Cdh10 cadherin 10 gene MP:0005013 increased lymphocyte cell number IEA N RGD:5509061 20231207 MGI 736214 Sctr secretin receptor gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0001405 impaired coordination IAGP N RGD:5509061 20161216 MGI PMID:17008357 736214 Sctr secretin receptor gene MP:0001422 abnormal drinking behavior IAGP N RGD:5509061 20141003 MGI PMID:20739612 736214 Sctr secretin receptor gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20161216 MGI PMID:17008357 736214 Sctr secretin receptor gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20161216 MGI PMID:17008357 736214 Sctr secretin receptor gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20161216 MGI PMID:17008357 736214 Sctr secretin receptor gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20161216 MGI PMID:17008357 736214 Sctr secretin receptor gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0003014 abnormal kidney medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:20739612 736214 Sctr secretin receptor gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0005609 abnormal circulating antidiuretic hormone level IAGP N RGD:5509061 20141003 MGI PMID:20739612 736214 Sctr secretin receptor gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20161216 MGI PMID:17008357 736214 Sctr secretin receptor gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0011467 decreased urine urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:17283064 736214 Sctr secretin receptor gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20161216 MGI PMID:17008357 736214 Sctr secretin receptor gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20161216 MGI PMID:17008357 736214 Sctr secretin receptor gene MP:0020396 abnormal social recognition IAGP N RGD:5509061 20161216 MGI PMID:17008357 736214 Sctr secretin receptor gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:17008357 736218 Cyp2d22 cytochrome P450, family 2, subfamily d, polypeptide 22 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 736218 Cyp2d22 cytochrome P450, family 2, subfamily d, polypeptide 22 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20221215 MGI 736218 Cyp2d22 cytochrome P450, family 2, subfamily d, polypeptide 22 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 736220 Plin1 perilipin 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0001553 abnormal circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0001553 abnormal circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:16595669 736220 Plin1 perilipin 1 gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17401109 736220 Plin1 perilipin 1 gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:17401109 736220 Plin1 perilipin 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20160407 MGI PMID:17401109 736220 Plin1 perilipin 1 gene MP:0003213 decreased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0003439 abnormal glycerol level IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0003457 abnormal circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18719666 736220 Plin1 perilipin 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:16595669 736220 Plin1 perilipin 1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0008032 abnormal lipolysis IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:16595669 736220 Plin1 perilipin 1 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:16595669 736220 Plin1 perilipin 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0009125 decreased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0009137 decreased brown fat lipid droplet number IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0009295 decreased interscapular fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0009301 decreased parametrial fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0009421 increased gastrocnemius weight IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11371650 736220 Plin1 perilipin 1 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:17401109 736220 Plin1 perilipin 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:11101849 736220 Plin1 perilipin 1 gene MP:0014144 abnormal white adipose tissue mass IAGP N RGD:5509061 20160407 MGI PMID:17401109 736220 Plin1 perilipin 1 gene MP:0014146 decreased white adipose tissue mass IAGP N RGD:5509061 20160407 MGI PMID:17401109 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20190124 MGI PMID:30356113 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20190124 MGI PMID:30356113 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20180315 MGI PMID:28005395 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20180315 MGI PMID:28005395 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20160623 MGI PMID:26046438 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20190124 MGI PMID:30356113 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20190124 MGI PMID:30356113 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20190124 MGI PMID:30356113 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20190124 MGI PMID:30356113 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20180315 MGI PMID:28005395 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20180315 MGI PMID:28005395 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0009082 uterus cyst IAGP N RGD:5509061 20180315 MGI PMID:28005395 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0009094 abnormal endometrial gland morphology IAGP N RGD:5509061 20180315 MGI PMID:28005395 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0009121 increased white fat cell lipid droplet size IAGP N RGD:5509061 20190124 MGI PMID:30356113 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0009251 enlarged endometrial glands IAGP N RGD:5509061 20180315 MGI PMID:28005395 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20190124 MGI PMID:30356113 736221 Pgrmc1 progesterone receptor membrane component 1 gene MP:0013401 increased endometrial gland number IAGP N RGD:5509061 20180315 MGI PMID:28005395 736225 Gdf11 growth differentiation factor 11 gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:23918385 736225 Gdf11 growth differentiation factor 11 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:24019467 736225 Gdf11 growth differentiation factor 11 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0000155 asymmetric rib joints IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20190502 MGI 736225 Gdf11 growth differentiation factor 11 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0000464 increased presacral vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:15548585 736225 Gdf11 growth differentiation factor 11 gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15548585 736225 Gdf11 growth differentiation factor 11 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:18519639 736225 Gdf11 growth differentiation factor 11 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:23918385 736225 Gdf11 growth differentiation factor 11 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:24019467 736225 Gdf11 growth differentiation factor 11 gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 736225 Gdf11 growth differentiation factor 11 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:12729564 736225 Gdf11 growth differentiation factor 11 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:18519639 736225 Gdf11 growth differentiation factor 11 gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:12546816 736225 Gdf11 growth differentiation factor 11 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:12729564 736225 Gdf11 growth differentiation factor 11 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:23918385 736225 Gdf11 growth differentiation factor 11 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:15548585 736225 Gdf11 growth differentiation factor 11 gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 736225 Gdf11 growth differentiation factor 11 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 736225 Gdf11 growth differentiation factor 11 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:15976303 736225 Gdf11 growth differentiation factor 11 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15976303 736225 Gdf11 growth differentiation factor 11 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:12546816 736225 Gdf11 growth differentiation factor 11 gene MP:0001539 decreased caudal vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:15548585 736225 Gdf11 growth differentiation factor 11 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20240229 MGI PMID:30661984 736225 Gdf11 growth differentiation factor 11 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:24019467 736225 Gdf11 growth differentiation factor 11 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0002809 increased spinal cord size IAGP N RGD:5509061 20240229 MGI PMID:30661984 736225 Gdf11 growth differentiation factor 11 gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:15976303 736225 Gdf11 growth differentiation factor 11 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:12729564 736225 Gdf11 growth differentiation factor 11 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12546816 736225 Gdf11 growth differentiation factor 11 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:24019467 736225 Gdf11 growth differentiation factor 11 gene MP:0003050 abnormal sacral vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0003052 omphalocele IAGP N RGD:5509061 20141003 MGI PMID:18519639 736225 Gdf11 growth differentiation factor 11 gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:12546816 736225 Gdf11 growth differentiation factor 11 gene MP:0003456 absent tail IAGP N RGD:5509061 20141003 MGI PMID:18519639 736225 Gdf11 growth differentiation factor 11 gene MP:0003604 single kidney IAGP N RGD:5509061 20141003 MGI PMID:12729564 736225 Gdf11 growth differentiation factor 11 gene MP:0003722 absent ureter IAGP N RGD:5509061 20141003 MGI PMID:12729564 736225 Gdf11 growth differentiation factor 11 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20210520 MGI 736225 Gdf11 growth differentiation factor 11 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 736225 Gdf11 growth differentiation factor 11 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20240229 MGI PMID:30661984 736225 Gdf11 growth differentiation factor 11 gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0004508 abnormal pectoral girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0004645 decreased vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0004650 increased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0004650 increased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:24019467 736225 Gdf11 growth differentiation factor 11 gene MP:0004651 increased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:18519639 736225 Gdf11 growth differentiation factor 11 gene MP:0004651 increased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0004651 increased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:24019467 736225 Gdf11 growth differentiation factor 11 gene MP:0004656 absent sacral vertebrae IAGP N RGD:5509061 20141003 MGI PMID:12546816 736225 Gdf11 growth differentiation factor 11 gene MP:0004656 absent sacral vertebrae IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 736225 Gdf11 growth differentiation factor 11 gene MP:0004936 impaired branching involved in ureteric bud morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12729564 736225 Gdf11 growth differentiation factor 11 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:15976303 736225 Gdf11 growth differentiation factor 11 gene MP:0005034 abnormal anus morphology IAGP N RGD:5509061 20141003 MGI PMID:18519639 736225 Gdf11 growth differentiation factor 11 gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:15548585 736225 Gdf11 growth differentiation factor 11 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15548585 736225 Gdf11 growth differentiation factor 11 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12729564 736225 Gdf11 growth differentiation factor 11 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15976303 736225 Gdf11 growth differentiation factor 11 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12546816 736225 Gdf11 growth differentiation factor 11 gene MP:0006095 absent amacrine cells IAGP N RGD:5509061 20141003 MGI PMID:15976303 736225 Gdf11 growth differentiation factor 11 gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:24019467 736225 Gdf11 growth differentiation factor 11 gene MP:0008514 absent retina inner plexiform layer IAGP N RGD:5509061 20141003 MGI PMID:15976303 736225 Gdf11 growth differentiation factor 11 gene MP:0008787 abnormal tailgut morphology IAGP N RGD:5509061 20240229 MGI PMID:30661984 736225 Gdf11 growth differentiation factor 11 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12546816 736225 Gdf11 growth differentiation factor 11 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:15548585 736225 Gdf11 growth differentiation factor 11 gene MP:0009149 decreased pancreatic acinar cell number IAGP N RGD:5509061 20141003 MGI PMID:15548585 736225 Gdf11 growth differentiation factor 11 gene MP:0009167 increased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:15548585 736225 Gdf11 growth differentiation factor 11 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:15548585 736225 Gdf11 growth differentiation factor 11 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:15548585 736225 Gdf11 growth differentiation factor 11 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:12546816 736225 Gdf11 growth differentiation factor 11 gene MP:0010978 absent ureteric bud IAGP N RGD:5509061 20141003 MGI PMID:12729564 736225 Gdf11 growth differentiation factor 11 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10391213 736225 Gdf11 growth differentiation factor 11 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12546816 736225 Gdf11 growth differentiation factor 11 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736225 Gdf11 growth differentiation factor 11 gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:12729564 736225 Gdf11 growth differentiation factor 11 gene MP:0011364 abnormal metanephros morphology IAGP N RGD:5509061 20141003 MGI PMID:12729564 736225 Gdf11 growth differentiation factor 11 gene MP:0011951 increased cardiac stroke volume IEA N RGD:5509061 20210128 MGI 736225 Gdf11 growth differentiation factor 11 gene MP:0012536 delayed optic fissure closure IAGP N RGD:5509061 20141003 MGI PMID:15976303 736225 Gdf11 growth differentiation factor 11 gene MP:0013167 abnormal hindlimb bud morphology IAGP N RGD:5509061 20231130 MGI PMID:12546816 736225 Gdf11 growth differentiation factor 11 gene MP:0013175 bifurcated tail IAGP N RGD:5509061 20240229 MGI PMID:30661984 736225 Gdf11 growth differentiation factor 11 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:19298661 736225 Gdf11 growth differentiation factor 11 gene MP:0030589 increased pancreatic alpha cell mass IAGP N RGD:5509061 20180614 MGI PMID:15548585 736228 Slc16a8 solute carrier family 16 (monocarboxylic acid transporters), member 8 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18524945 736230 Mlst8 MTOR associated protein, LST8 homolog (S. cerevisiae) gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:17141160 736230 Mlst8 MTOR associated protein, LST8 homolog (S. cerevisiae) gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:17141160 736230 Mlst8 MTOR associated protein, LST8 homolog (S. cerevisiae) gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:17141160 736230 Mlst8 MTOR associated protein, LST8 homolog (S. cerevisiae) gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17141160 736230 Mlst8 MTOR associated protein, LST8 homolog (S. cerevisiae) gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:19185849 736230 Mlst8 MTOR associated protein, LST8 homolog (S. cerevisiae) gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17141160 736230 Mlst8 MTOR associated protein, LST8 homolog (S. cerevisiae) gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:17141160 736230 Mlst8 MTOR associated protein, LST8 homolog (S. cerevisiae) gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17141160 736230 Mlst8 MTOR associated protein, LST8 homolog (S. cerevisiae) gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17141160 736230 Mlst8 MTOR associated protein, LST8 homolog (S. cerevisiae) gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:17141160 736230 Mlst8 MTOR associated protein, LST8 homolog (S. cerevisiae) gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17141160 736230 Mlst8 MTOR associated protein, LST8 homolog (S. cerevisiae) gene MP:0011524 thick placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:17141160 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20170119 MGI PMID:27903723 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:22699620 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22699620 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20170119 MGI PMID:27903723 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001384 abnormal pup retrieval IAGP N RGD:5509061 20141003 MGI PMID:22699620 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210128 MGI 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22699620 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170119 MGI PMID:27903723 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20170119 MGI PMID:27903723 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:22699620 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:22699620 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:22699620 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22699620 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001475 reduced long-term depression IAGP N RGD:5509061 20141003 MGI PMID:22699620 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:22699620 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0002797 increased thigmotaxis IEA N RGD:5509061 20210128 MGI 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0002863 improved righting response IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20201022 MGI 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20141003 MGI PMID:22699620 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:22699620 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20170119 MGI PMID:27903723 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20210128 MGI 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20211021 MGI 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0012440 abnormal neutrophil cell number IEA N RGD:5509061 20211021 MGI 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20161013 MGI PMID:22699620 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0020357 abnormal excitatory synapse morphology IAGP N RGD:5509061 20170119 MGI PMID:27903723 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22699619 736233 Shank2 SH3 and multiple ankyrin repeat domains 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:22699620 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20151112 MGI PMID:18644395 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20181227 MGI 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:22082674 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22082674 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18768391 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:22082674 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22082674 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22082674 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:22082674 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:22082674 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:22082674 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22082674 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20160421 MGI 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:22082674 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:19124833 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160421 MGI 736234 Pak1 p21 (RAC1) activated kinase 1 gene MP:0020438 decreased papilloma incidence IAGP N RGD:5509061 20220623 MGI PMID:35240107 736237 Otx1 orthodenticle homeobox 1 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:10068635 736237 Otx1 orthodenticle homeobox 1 gene MP:0000036 absent semicircular canals IAGP N RGD:5509061 20141003 MGI PMID:8841200 736237 Otx1 orthodenticle homeobox 1 gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:10068635 736237 Otx1 orthodenticle homeobox 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0000776 abnormal inferior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0000777 increased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:8841200 736237 Otx1 orthodenticle homeobox 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 736237 Otx1 orthodenticle homeobox 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 736237 Otx1 orthodenticle homeobox 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 736237 Otx1 orthodenticle homeobox 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 736237 Otx1 orthodenticle homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10068635 736237 Otx1 orthodenticle homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 736237 Otx1 orthodenticle homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20816794 736237 Otx1 orthodenticle homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:8841200 736237 Otx1 orthodenticle homeobox 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 736237 Otx1 orthodenticle homeobox 1 gene MP:0000815 abnormal Ammon gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 736237 Otx1 orthodenticle homeobox 1 gene MP:0000826 abnormal third ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 736237 Otx1 orthodenticle homeobox 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:10068635 736237 Otx1 orthodenticle homeobox 1 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:8841200 736237 Otx1 orthodenticle homeobox 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 736237 Otx1 orthodenticle homeobox 1 gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0000905 increased superior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:8841200 736237 Otx1 orthodenticle homeobox 1 gene MP:0000906 abnormal trigeminal V mesencephalic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:15201224 736237 Otx1 orthodenticle homeobox 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:9895322 736237 Otx1 orthodenticle homeobox 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:10068635 736237 Otx1 orthodenticle homeobox 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:8841200 736237 Otx1 orthodenticle homeobox 1 gene MP:0000948 nonconvulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:8841200 736237 Otx1 orthodenticle homeobox 1 gene MP:0001061 abnormal oculomotor nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0001063 abnormal trochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:9477321 736237 Otx1 orthodenticle homeobox 1 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:9477321 736237 Otx1 orthodenticle homeobox 1 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9477321 736237 Otx1 orthodenticle homeobox 1 gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:9477321 736237 Otx1 orthodenticle homeobox 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9477321 736237 Otx1 orthodenticle homeobox 1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:8841200 736237 Otx1 orthodenticle homeobox 1 gene MP:0001322 abnormal iris morphology IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0001329 retina hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20141003 MGI PMID:10068635 736237 Otx1 orthodenticle homeobox 1 gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20141003 MGI PMID:8841200 736237 Otx1 orthodenticle homeobox 1 gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20141204 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0001394 circling IEA N RGD:5509061 20111116 MGI 736237 Otx1 orthodenticle homeobox 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9477321 736237 Otx1 orthodenticle homeobox 1 gene MP:0001746 abnormal pituitary secretion IAGP N RGD:5509061 20141003 MGI PMID:9477321 736237 Otx1 orthodenticle homeobox 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10068635 736237 Otx1 orthodenticle homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9477321 736237 Otx1 orthodenticle homeobox 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:10068635 736237 Otx1 orthodenticle homeobox 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:9477321 736237 Otx1 orthodenticle homeobox 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:9477321 736237 Otx1 orthodenticle homeobox 1 gene MP:0002683 delayed fertility IAGP N RGD:5509061 20141003 MGI PMID:9477321 736237 Otx1 orthodenticle homeobox 1 gene MP:0002730 head shaking IEA N RGD:5509061 20111116 MGI 736237 Otx1 orthodenticle homeobox 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:9477321 736237 Otx1 orthodenticle homeobox 1 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12764108 736237 Otx1 orthodenticle homeobox 1 gene MP:0002892 decreased superior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:10068635 736237 Otx1 orthodenticle homeobox 1 gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12764108 736237 Otx1 orthodenticle homeobox 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0003877 abnormal serotonergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12764108 736237 Otx1 orthodenticle homeobox 1 gene MP:0004162 abnormal mammillary body morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20150122 MGI PMID:24457099 736237 Otx1 orthodenticle homeobox 1 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20816794 736237 Otx1 orthodenticle homeobox 1 gene MP:0004280 abnormal oculomotor nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0004450 presphenoid bone hypoplasia IAGP N RGD:5509061 20171207 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0004457 abnormal orbitosphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0004463 basisphenoid bone foramen IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:12652306 736237 Otx1 orthodenticle homeobox 1 gene MP:0005205 abnormal eye anterior chamber morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0006089 abnormal vestibular saccule morphology IEA N RGD:5509061 20111116 MGI 736237 Otx1 orthodenticle homeobox 1 gene MP:0006090 abnormal utricle morphology IEA N RGD:5509061 20111116 MGI 736237 Otx1 orthodenticle homeobox 1 gene MP:0006100 abnormal tegmentum morphology IAGP N RGD:5509061 20141003 MGI PMID:12652306 736237 Otx1 orthodenticle homeobox 1 gene MP:0006100 abnormal tegmentum morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0006101 absent tegmentum IAGP N RGD:5509061 20141003 MGI PMID:20816794 736237 Otx1 orthodenticle homeobox 1 gene MP:0006105 small tectum IAGP N RGD:5509061 20141003 MGI PMID:12652306 736237 Otx1 orthodenticle homeobox 1 gene MP:0006106 absent tectum IAGP N RGD:5509061 20141003 MGI PMID:20816794 736237 Otx1 orthodenticle homeobox 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0008283 small hippocampus IAGP N RGD:5509061 20141003 MGI PMID:9895322 736237 Otx1 orthodenticle homeobox 1 gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 736237 Otx1 orthodenticle homeobox 1 gene MP:0008881 absent Harderian gland IAGP N RGD:5509061 20141003 MGI PMID:10068635 736237 Otx1 orthodenticle homeobox 1 gene MP:0008881 absent Harderian gland IAGP N RGD:5509061 20141003 MGI PMID:8841200 736237 Otx1 orthodenticle homeobox 1 gene MP:0008881 absent Harderian gland IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0008914 enlarged cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0008914 enlarged cerebellum IAGP N RGD:5509061 20141003 MGI PMID:9895322 736237 Otx1 orthodenticle homeobox 1 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0009637 abnormal pretectal region morphology IAGP N RGD:5509061 20141003 MGI PMID:15917450 736237 Otx1 orthodenticle homeobox 1 gene MP:0009637 abnormal pretectal region morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 736237 Otx1 orthodenticle homeobox 1 gene MP:0010893 abnormal posterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12652306 736237 Otx1 orthodenticle homeobox 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9521907 736237 Otx1 orthodenticle homeobox 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20141204 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:15201224 736237 Otx1 orthodenticle homeobox 1 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:20816794 736237 Otx1 orthodenticle homeobox 1 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:10068635 736237 Otx1 orthodenticle homeobox 1 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:9895322 736237 Otx1 orthodenticle homeobox 1 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:12652306 736237 Otx1 orthodenticle homeobox 1 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:20816794 736237 Otx1 orthodenticle homeobox 1 gene MP:0012132 abnormal midbrain-hindbrain boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:9895322 736237 Otx1 orthodenticle homeobox 1 gene MP:0012267 abnormal red nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0012517 absent diencephalon IAGP N RGD:5509061 20141003 MGI PMID:15201224 736237 Otx1 orthodenticle homeobox 1 gene MP:0012517 absent diencephalon IAGP N RGD:5509061 20141003 MGI PMID:20816794 736237 Otx1 orthodenticle homeobox 1 gene MP:0012525 abnormal rhombic lip morphology IAGP N RGD:5509061 20141003 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0012786 increased rhombomere 1 size IAGP N RGD:5509061 20141003 MGI PMID:9895322 736237 Otx1 orthodenticle homeobox 1 gene MP:0014165 absent ciliary process IAGP N RGD:5509061 20160414 MGI PMID:10068635 736237 Otx1 orthodenticle homeobox 1 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:15917450 736237 Otx1 orthodenticle homeobox 1 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:9895322 736237 Otx1 orthodenticle homeobox 1 gene MP:0020531 increased cerebellar foliation IAGP N RGD:5509061 20180301 MGI PMID:8841200 736237 Otx1 orthodenticle homeobox 1 gene MP:0020534 increased pons size IAGP N RGD:5509061 20180301 MGI PMID:20816794 736237 Otx1 orthodenticle homeobox 1 gene MP:0020534 increased pons size IAGP N RGD:5509061 20180301 MGI PMID:9895322 736237 Otx1 orthodenticle homeobox 1 gene MP:0020543 decreased substantia nigra size IAGP N RGD:5509061 20180301 MGI PMID:9077465 736237 Otx1 orthodenticle homeobox 1 gene MP:0031442 enlarged cerebral aqueduct IAGP N RGD:5509061 20221103 MGI PMID:9077465 736240 Pitpnb phosphatidylinositol transfer protein, beta gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11907258 736241 Jag2 jagged 2 gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:16141228 736241 Jag2 jagged 2 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:20533406 736241 Jag2 jagged 2 gene MP:0000430 absent maxillary shelf IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0000431 absent palatine bone horizontal plate IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:20533406 736241 Jag2 jagged 2 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20111116 MGI 736241 Jag2 jagged 2 gene MP:0000585 kinked tail IEA N RGD:5509061 20111116 MGI 736241 Jag2 jagged 2 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0001222 epidermal hyperplasia IEA N RGD:5509061 20111116 MGI 736241 Jag2 jagged 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0001676 abnormal apical ectodermal ridge morphology IEA N RGD:5509061 20111229 MGI 736241 Jag2 jagged 2 gene MP:0001678 thick apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:4305644 736241 Jag2 jagged 2 gene MP:0001678 thick apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0001926 female infertility IEA N RGD:5509061 20111116 MGI 736241 Jag2 jagged 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20111116 MGI 736241 Jag2 jagged 2 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0002622 abnormal cochlear hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16141228 736241 Jag2 jagged 2 gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20111116 MGI 736241 Jag2 jagged 2 gene MP:0003427 parakeratosis IEA N RGD:5509061 20111116 MGI 736241 Jag2 jagged 2 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10080181 736241 Jag2 jagged 2 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10837254 736241 Jag2 jagged 2 gene MP:0004395 increased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16141228 736241 Jag2 jagged 2 gene MP:0004396 decreased cochlear inner hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10837254 736241 Jag2 jagged 2 gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10837254 736241 Jag2 jagged 2 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10080181 736241 Jag2 jagged 2 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10837254 736241 Jag2 jagged 2 gene MP:0004401 increased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:16141228 736241 Jag2 jagged 2 gene MP:0004407 increased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10080181 736241 Jag2 jagged 2 gene MP:0004407 increased cochlear hair cell number IAGP N RGD:5509061 20141003 MGI PMID:10837254 736241 Jag2 jagged 2 gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:10080181 736241 Jag2 jagged 2 gene MP:0004497 decreased organ of Corti supporting cell number IAGP N RGD:5509061 20141003 MGI PMID:10080181 736241 Jag2 jagged 2 gene MP:0004497 decreased organ of Corti supporting cell number IAGP N RGD:5509061 20141003 MGI PMID:16141228 736241 Jag2 jagged 2 gene MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:16141228 736241 Jag2 jagged 2 gene MP:0004576 abnormal embryonic autopod plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:4305644 736241 Jag2 jagged 2 gene MP:0006280 abnormal digit development IEA N RGD:5509061 20111116 MGI 736241 Jag2 jagged 2 gene MP:0008347 decreased gamma-delta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0008356 abnormal gamma-delta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0008730 fused phalanges IEA N RGD:5509061 20111116 MGI 736241 Jag2 jagged 2 gene MP:0008919 fused tarsal bones IEA N RGD:5509061 20111116 MGI 736241 Jag2 jagged 2 gene MP:0009884 palatal shelf fusion with tongue or mandible IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0009884 palatal shelf fusion with tongue or mandible IAGP N RGD:5509061 20171214 MGI PMID:20533406 736241 Jag2 jagged 2 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16141228 736241 Jag2 jagged 2 gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 736241 Jag2 jagged 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20533406 736241 Jag2 jagged 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9531541 736241 Jag2 jagged 2 gene MP:0011090 perinatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 736241 Jag2 jagged 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736241 Jag2 jagged 2 gene MP:0021210 bilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:9531541 736243 Spag5 sperm associated antigen 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11884588 736244 Nfasc neurofascin gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:20188654 736244 Nfasc neurofascin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19185024 736244 Nfasc neurofascin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20371806 736244 Nfasc neurofascin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20371806 736244 Nfasc neurofascin gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19185024 736244 Nfasc neurofascin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19185024 736244 Nfasc neurofascin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20371806 736244 Nfasc neurofascin gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21382554 736244 Nfasc neurofascin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21382554 736244 Nfasc neurofascin gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:19185024 736244 Nfasc neurofascin gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:19185024 736244 Nfasc neurofascin gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:21382554 736244 Nfasc neurofascin gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20160804 MGI 736244 Nfasc neurofascin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19185024 736244 Nfasc neurofascin gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:19185024 736244 Nfasc neurofascin gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:21382554 736244 Nfasc neurofascin gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16337912 736244 Nfasc neurofascin gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:19185024 736244 Nfasc neurofascin gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:21382554 736244 Nfasc neurofascin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:18573915 736244 Nfasc neurofascin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19185024 736244 Nfasc neurofascin gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:20188654 736244 Nfasc neurofascin gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:16337912 736244 Nfasc neurofascin gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:19185024 736244 Nfasc neurofascin gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18573915 736244 Nfasc neurofascin gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:21382554 736244 Nfasc neurofascin gene MP:0010733 abnormal axon initial segment morphology IAGP N RGD:5509061 20141003 MGI PMID:21382554 736244 Nfasc neurofascin gene MP:0010734 abnormal paranode morphology IAGP N RGD:5509061 20141003 MGI PMID:20371806 736244 Nfasc neurofascin gene MP:0010735 abnormal paranodal axoglial junction morphology IAGP N RGD:5509061 20141003 MGI PMID:20371806 736244 Nfasc neurofascin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16337912 736244 Nfasc neurofascin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18573915 736244 Nfasc neurofascin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19185024 736244 Nfasc neurofascin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20188654 736244 Nfasc neurofascin gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:19185024 736246 Hoxa4 homeobox A4 gene MP:0000155 asymmetric rib joints IAGP N RGD:5509061 20141003 MGI PMID:7809093 736246 Hoxa4 homeobox A4 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:7628700 736246 Hoxa4 homeobox A4 gene MP:0000480 increased rib number IAGP N RGD:5509061 20141003 MGI PMID:7809093 736246 Hoxa4 homeobox A4 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 736246 Hoxa4 homeobox A4 gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 736246 Hoxa4 homeobox A4 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20220811 MGI 736246 Hoxa4 homeobox A4 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:7918106 736246 Hoxa4 homeobox A4 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 736246 Hoxa4 homeobox A4 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 736246 Hoxa4 homeobox A4 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7628700 736246 Hoxa4 homeobox A4 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7809093 736246 Hoxa4 homeobox A4 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:7918106 736246 Hoxa4 homeobox A4 gene MP:0004508 abnormal pectoral girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:7918106 736246 Hoxa4 homeobox A4 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7628700 736246 Hoxa4 homeobox A4 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:7809093 736246 Hoxa4 homeobox A4 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:7628700 736246 Hoxa4 homeobox A4 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:7809093 736246 Hoxa4 homeobox A4 gene MP:0010082 sternebra fusion IAGP N RGD:5509061 20141003 MGI PMID:7809093 736246 Hoxa4 homeobox A4 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7628700 736249 Gpr135 G protein-coupled receptor 135 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 736252 Cnn1 calponin 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:9893025 736252 Cnn1 calponin 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:9893025 736252 Cnn1 calponin 1 gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20141003 MGI PMID:9893025 736252 Cnn1 calponin 1 gene MP:0003416 premature bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9893025 736252 Cnn1 calponin 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:9893025 736252 Cnn1 calponin 1 gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:9893025 736252 Cnn1 calponin 1 gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:9893025 736252 Cnn1 calponin 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21817093 736252 Cnn1 calponin 1 gene MP:0011710 enhanced osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:9893025 736252 Cnn1 calponin 1 gene MP:0014167 ectopic bone IAGP N RGD:5509061 20160407 MGI PMID:9893025 736257 Robo2 roundabout guidance receptor 2 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:23328398 736257 Robo2 roundabout guidance receptor 2 gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20141003 MGI PMID:17357069 736257 Robo2 roundabout guidance receptor 2 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:17357069 736257 Robo2 roundabout guidance receptor 2 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:15130495 736257 Robo2 roundabout guidance receptor 2 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:17357069 736257 Robo2 roundabout guidance receptor 2 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:17392456 736257 Robo2 roundabout guidance receptor 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:21613506 736257 Robo2 roundabout guidance receptor 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160211 MGI PMID:24607227 736257 Robo2 roundabout guidance receptor 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:23328398 736257 Robo2 roundabout guidance receptor 2 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 736257 Robo2 roundabout guidance receptor 2 gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 736257 Robo2 roundabout guidance receptor 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:23328398 736257 Robo2 roundabout guidance receptor 2 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:23328398 736257 Robo2 roundabout guidance receptor 2 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20141003 MGI PMID:21613506 736257 Robo2 roundabout guidance receptor 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:17357069 736257 Robo2 roundabout guidance receptor 2 gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210826 MGI 736257 Robo2 roundabout guidance receptor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17357069 736257 Robo2 roundabout guidance receptor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23328398 736257 Robo2 roundabout guidance receptor 2 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:17392456 736257 Robo2 roundabout guidance receptor 2 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:23328398 736257 Robo2 roundabout guidance receptor 2 gene MP:0002769 abnormal vas deferens morphology IAGP N RGD:5509061 20141003 MGI PMID:17357069 736257 Robo2 roundabout guidance receptor 2 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15084255 736257 Robo2 roundabout guidance receptor 2 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15091338 736257 Robo2 roundabout guidance receptor 2 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:17360927 736257 Robo2 roundabout guidance receptor 2 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:17392456 736257 Robo2 roundabout guidance receptor 2 gene MP:0002990 short ureter IAGP N RGD:5509061 20141003 MGI PMID:17357069 736257 Robo2 roundabout guidance receptor 2 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210826 MGI 736257 Robo2 roundabout guidance receptor 2 gene MP:0003585 large ureter IAGP N RGD:5509061 20141003 MGI PMID:17357069 736257 Robo2 roundabout guidance receptor 2 gene MP:0003586 dilated ureter IAGP N RGD:5509061 20141003 MGI PMID:17357069 736257 Robo2 roundabout guidance receptor 2 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17357069 736257 Robo2 roundabout guidance receptor 2 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:23328398 736257 Robo2 roundabout guidance receptor 2 gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18054781 736257 Robo2 roundabout guidance receptor 2 gene MP:0004550 short trachea IAGP N RGD:5509061 20141003 MGI PMID:23328398 736257 Robo2 roundabout guidance receptor 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:23328398 736257 Robo2 roundabout guidance receptor 2 gene MP:0005237 abnormal olfactory tract morphology IAGP N RGD:5509061 20141003 MGI PMID:17360927 736257 Robo2 roundabout guidance receptor 2 gene MP:0008219 abnormal dorsal telencephalic commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:17392456 736257 Robo2 roundabout guidance receptor 2 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:17392456 736257 Robo2 roundabout guidance receptor 2 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:18054781 736257 Robo2 roundabout guidance receptor 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20160211 MGI PMID:24607227 736257 Robo2 roundabout guidance receptor 2 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:23328398 736257 Robo2 roundabout guidance receptor 2 gene MP:0009678 abnormal spinal cord lateral column morphology IAGP N RGD:5509061 20141003 MGI PMID:15091338 736257 Robo2 roundabout guidance receptor 2 gene MP:0009695 abnormal spinal cord ventral commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:23217742 736257 Robo2 roundabout guidance receptor 2 gene MP:0009976 abnormal cerebellar peduncle morphology IAGP N RGD:5509061 20171102 MGI PMID:17392456 736257 Robo2 roundabout guidance receptor 2 gene MP:0010807 abnormal stomach position or orientation IAGP N RGD:5509061 20141003 MGI PMID:23328398 736257 Robo2 roundabout guidance receptor 2 gene MP:0010880 small esophagus IAGP N RGD:5509061 20141003 MGI PMID:23328398 736257 Robo2 roundabout guidance receptor 2 gene MP:0010881 esophagus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23328398 736257 Robo2 roundabout guidance receptor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15130495 736257 Robo2 roundabout guidance receptor 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17357069 736257 Robo2 roundabout guidance receptor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23328398 736257 Robo2 roundabout guidance receptor 2 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18054781 736257 Robo2 roundabout guidance receptor 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736257 Robo2 roundabout guidance receptor 2 gene MP:0011488 abnormal ureterovesical junction morphology IAGP N RGD:5509061 20141003 MGI PMID:17357069 736257 Robo2 roundabout guidance receptor 2 gene MP:0011492 ureterovesical junction obstruction IAGP N RGD:5509061 20141003 MGI PMID:17357069 736257 Robo2 roundabout guidance receptor 2 gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20141003 MGI PMID:23328398 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15911877 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:15911877 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15911877 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11430819 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:11430819 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11430819 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15911877 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11430819 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15911877 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:11430819 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11430819 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0002791 steatorrhea IAGP N RGD:5509061 20141003 MGI PMID:11430819 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:15911877 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0003335 exocrine pancreatic insufficiency IAGP N RGD:5509061 20141003 MGI PMID:11430819 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0003335 exocrine pancreatic insufficiency IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:11430819 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:17727724 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0003340 acute pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:17727724 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11430819 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:17727724 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:11430819 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:11430819 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0005220 abnormal exocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:17727724 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11430819 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17765679 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0008027 abnormal spinal cord white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:15911877 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0008806 increased circulating amylase level IAGP N RGD:5509061 20150611 MGI PMID:17727724 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17765679 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0009145 abnormal pancreatic acinus morphology IAGP N RGD:5509061 20141003 MGI PMID:17727724 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17727724 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0009164 exocrine pancreas atrophy IAGP N RGD:5509061 20141003 MGI PMID:17727724 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0009174 absent pancreatic beta cells IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:11430819 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0009178 absent pancreatic alpha cells IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0010205 abnormal oligodendrocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15911877 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20150611 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11430819 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15911877 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0012432 decreased prostate gland tumor incidence IAGP N RGD:5509061 20181004 MGI PMID:29720449 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0013182 increased spinal cord apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15911877 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:11997520 736260 Eif2ak3 eukaryotic translation initiation factor 2 alpha kinase 3 gene MP:0030441 increased osteoblast apoptosis IAGP N RGD:5509061 20171221 MGI PMID:11997520 736266 Trim28 tripartite motif-containing 28 gene MP:0000929 open neural tube IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20230601 MGI PMID:35906245 736266 Trim28 tripartite motif-containing 28 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:10851139 736266 Trim28 tripartite motif-containing 28 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:10851139 736266 Trim28 tripartite motif-containing 28 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:21163256 736266 Trim28 tripartite motif-containing 28 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:10851139 736266 Trim28 tripartite motif-containing 28 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:19099580 736266 Trim28 tripartite motif-containing 28 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:21163256 736266 Trim28 tripartite motif-containing 28 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:19099580 736266 Trim28 tripartite motif-containing 28 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:21163256 736266 Trim28 tripartite motif-containing 28 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10851139 736266 Trim28 tripartite motif-containing 28 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0002210 abnormal sex determination IAGP N RGD:5509061 20141003 MGI PMID:19099580 736266 Trim28 tripartite motif-containing 28 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:21163256 736266 Trim28 tripartite motif-containing 28 gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20141003 MGI PMID:21163256 736266 Trim28 tripartite motif-containing 28 gene MP:0003119 abnormal digestive system development IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:21163256 736266 Trim28 tripartite motif-containing 28 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21163256 736266 Trim28 tripartite motif-containing 28 gene MP:0004182 abnormal spermiation IAGP N RGD:5509061 20141003 MGI PMID:21163256 736266 Trim28 tripartite motif-containing 28 gene MP:0004558 delayed allantois development IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21163256 736266 Trim28 tripartite motif-containing 28 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:21163256 736266 Trim28 tripartite motif-containing 28 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:21163256 736266 Trim28 tripartite motif-containing 28 gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20230601 MGI PMID:35906245 736266 Trim28 tripartite motif-containing 28 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19099580 736266 Trim28 tripartite motif-containing 28 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10851139 736266 Trim28 tripartite motif-containing 28 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21163256 736266 Trim28 tripartite motif-containing 28 gene MP:0011200 abnormal extraembryonic coelom morphology IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0011202 abnormal ectoplacental cavity morphology IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0011203 abnormal parietal yolk sac morphology IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0012173 short rostral-caudal axis IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0012180 abnormal somatic mesoderm morphology IAGP N RGD:5509061 20150416 MGI PMID:22110054 736266 Trim28 tripartite motif-containing 28 gene MP:0013600 testis degeneration IAGP N RGD:5509061 20150312 MGI PMID:21163256 736268 Syn2 synapsin II gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:7777057 736268 Syn2 synapsin II gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:23280234 736268 Syn2 synapsin II gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:23280234 736268 Syn2 synapsin II gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:23280234 736268 Syn2 synapsin II gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:24009558 736268 Syn2 synapsin II gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:9513186 736268 Syn2 synapsin II gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:9513186 736268 Syn2 synapsin II gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:24009558 736268 Syn2 synapsin II gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:7777057 736268 Syn2 synapsin II gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:23280234 736268 Syn2 synapsin II gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9513186 736268 Syn2 synapsin II gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:24009558 736268 Syn2 synapsin II gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:7777057 736268 Syn2 synapsin II gene MP:0002917 decreased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:24009558 736268 Syn2 synapsin II gene MP:0002922 decreased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:7777057 736268 Syn2 synapsin II gene MP:0002924 delayed CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:9513186 736268 Syn2 synapsin II gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20151224 MGI PMID:21621590 736268 Syn2 synapsin II gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:24009558 736268 Syn2 synapsin II gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:24009558 736268 Syn2 synapsin II gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20151224 MGI PMID:21621590 736268 Syn2 synapsin II gene MP:0004996 abnormal CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:9513186 736268 Syn2 synapsin II gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20151224 MGI PMID:21621590 736268 Syn2 synapsin II gene MP:0012006 abnormal hippocampus physiology IAGP N RGD:5509061 20141003 MGI PMID:24009558 736268 Syn2 synapsin II gene MP:0021111 decreased social investigation IAGP N RGD:5509061 20240328 MGI PMID:23280234 736269 Rax retina and anterior neural fold homeobox gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:15789424 736269 Rax retina and anterior neural fold homeobox gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:9177348 736269 Rax retina and anterior neural fold homeobox gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:16850473 736269 Rax retina and anterior neural fold homeobox gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23209739 736269 Rax retina and anterior neural fold homeobox gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:15789424 736269 Rax retina and anterior neural fold homeobox gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:9177348 736269 Rax retina and anterior neural fold homeobox gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:15789424 736269 Rax retina and anterior neural fold homeobox gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:16850473 736269 Rax retina and anterior neural fold homeobox gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:17247120 736269 Rax retina and anterior neural fold homeobox gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:23209739 736269 Rax retina and anterior neural fold homeobox gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:640224 736269 Rax retina and anterior neural fold homeobox gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:9177348 736269 Rax retina and anterior neural fold homeobox gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:925203 736269 Rax retina and anterior neural fold homeobox gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:17247120 736269 Rax retina and anterior neural fold homeobox gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:23209739 736269 Rax retina and anterior neural fold homeobox gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:640224 736269 Rax retina and anterior neural fold homeobox gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:6201404 736269 Rax retina and anterior neural fold homeobox gene MP:0001306 small lens IAGP N RGD:5509061 20141003 MGI PMID:640224 736269 Rax retina and anterior neural fold homeobox gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20210708 MGI PMID:32801350 736269 Rax retina and anterior neural fold homeobox gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:925203 736269 Rax retina and anterior neural fold homeobox gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15789424 736269 Rax retina and anterior neural fold homeobox gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:13469955 736269 Rax retina and anterior neural fold homeobox gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15789424 736269 Rax retina and anterior neural fold homeobox gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:15789424 736269 Rax retina and anterior neural fold homeobox gene MP:0002984 retina hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22090505 736269 Rax retina and anterior neural fold homeobox gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20210708 MGI PMID:32801350 736269 Rax retina and anterior neural fold homeobox gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:16850473 736269 Rax retina and anterior neural fold homeobox gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:6201404 736269 Rax retina and anterior neural fold homeobox gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:640224 736269 Rax retina and anterior neural fold homeobox gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:9177348 736269 Rax retina and anterior neural fold homeobox gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:6201404 736269 Rax retina and anterior neural fold homeobox gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:640224 736269 Rax retina and anterior neural fold homeobox gene MP:0006294 absent optic vesicle IAGP N RGD:5509061 20141003 MGI PMID:9177348 736269 Rax retina and anterior neural fold homeobox gene MP:0008847 abnormal suprachiasmatic nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:925203 736269 Rax retina and anterior neural fold homeobox gene MP:0009392 retina gliosis IAGP N RGD:5509061 20210708 MGI PMID:32801350 736269 Rax retina and anterior neural fold homeobox gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20141003 MGI PMID:9177348 736269 Rax retina and anterior neural fold homeobox gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:9177348 736269 Rax retina and anterior neural fold homeobox gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:9177348 736269 Rax retina and anterior neural fold homeobox gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:10357435 736269 Rax retina and anterior neural fold homeobox gene MP:0030241 absent optic pit IAGP N RGD:5509061 20171109 MGI PMID:15789424 736269 Rax retina and anterior neural fold homeobox gene MP:0030241 absent optic pit IAGP N RGD:5509061 20171109 MGI PMID:9177348 736271 Smpx small muscle protein, X-linked gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11381084 736271 Smpx small muscle protein, X-linked gene MP:0004399 abnormal cochlear outer hair cell morphology IAGP N RGD:5509061 20220127 MGI PMID:34722533 736271 Smpx small muscle protein, X-linked gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20220127 MGI PMID:34722533 736271 Smpx small muscle protein, X-linked gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20220127 MGI PMID:34722533 736271 Smpx small muscle protein, X-linked gene MP:0004597 increased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20220127 MGI PMID:34722533 736271 Smpx small muscle protein, X-linked gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20220127 MGI PMID:34722533 736271 Smpx small muscle protein, X-linked gene MP:0004749 nonsyndromic hearing loss IAGP N RGD:5509061 20220127 MGI PMID:34722533 736271 Smpx small muscle protein, X-linked gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20220127 MGI PMID:34722533 736272 Hfe homeostatic iron regulator gene MP:0000066 osteoporosis IAGP N RGD:5509061 20180830 MGI PMID:20976594 736272 Hfe homeostatic iron regulator gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20180830 MGI PMID:20976594 736272 Hfe homeostatic iron regulator gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:15849611 736272 Hfe homeostatic iron regulator gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:16491649 736272 Hfe homeostatic iron regulator gene MP:0000771 abnormal brain size IAGP N RGD:5509061 20151112 MGI PMID:24439478 736272 Hfe homeostatic iron regulator gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20151112 MGI PMID:24439478 736272 Hfe homeostatic iron regulator gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:16491649 736272 Hfe homeostatic iron regulator gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23429074 736272 Hfe homeostatic iron regulator gene MP:0001260 increased body weight IAGP N RGD:5509061 20180830 MGI PMID:20976594 736272 Hfe homeostatic iron regulator gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16491649 736272 Hfe homeostatic iron regulator gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16491649 736272 Hfe homeostatic iron regulator gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20151112 MGI PMID:24439478 736272 Hfe homeostatic iron regulator gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20141003 MGI PMID:16491649 736272 Hfe homeostatic iron regulator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15849611 736272 Hfe homeostatic iron regulator gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:10381492 736272 Hfe homeostatic iron regulator gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20180830 MGI PMID:20976594 736272 Hfe homeostatic iron regulator gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10791995 736272 Hfe homeostatic iron regulator gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17264297 736272 Hfe homeostatic iron regulator gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20151112 MGI PMID:24439478 736272 Hfe homeostatic iron regulator gene MP:0002980 abnormal postural reflex IAGP N RGD:5509061 20141003 MGI PMID:16491649 736272 Hfe homeostatic iron regulator gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20151112 MGI PMID:24439478 736272 Hfe homeostatic iron regulator gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:23429074 736272 Hfe homeostatic iron regulator gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20151112 MGI PMID:24439478 736272 Hfe homeostatic iron regulator gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:23429074 736272 Hfe homeostatic iron regulator gene MP:0004147 increased porphyrin level IAGP N RGD:5509061 20141003 MGI PMID:11134514 736272 Hfe homeostatic iron regulator gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:18316026 736272 Hfe homeostatic iron regulator gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20180830 MGI PMID:20976594 736272 Hfe homeostatic iron regulator gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10557317 736272 Hfe homeostatic iron regulator gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17264297 736272 Hfe homeostatic iron regulator gene MP:0005638 hemochromatosis IAGP N RGD:5509061 20141003 MGI PMID:15131800 736272 Hfe homeostatic iron regulator gene MP:0005638 hemochromatosis IAGP N RGD:5509061 20141003 MGI PMID:17258727 736272 Hfe homeostatic iron regulator gene MP:0005638 hemochromatosis IAGP N RGD:5509061 20141003 MGI PMID:18249176 736272 Hfe homeostatic iron regulator gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:18316026 736272 Hfe homeostatic iron regulator gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20151112 MGI PMID:24439478 736272 Hfe homeostatic iron regulator gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20151112 MGI PMID:24439478 736272 Hfe homeostatic iron regulator gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:10791995 736272 Hfe homeostatic iron regulator gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:18316026 736272 Hfe homeostatic iron regulator gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:10557317 736272 Hfe homeostatic iron regulator gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:10791995 736272 Hfe homeostatic iron regulator gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:11134514 736272 Hfe homeostatic iron regulator gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:14618243 736272 Hfe homeostatic iron regulator gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:14673107 736272 Hfe homeostatic iron regulator gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:15849611 736272 Hfe homeostatic iron regulator gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:17264297 736272 Hfe homeostatic iron regulator gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:18249176 736272 Hfe homeostatic iron regulator gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:18316026 736272 Hfe homeostatic iron regulator gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:23429074 736272 Hfe homeostatic iron regulator gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20180830 MGI PMID:20976594 736272 Hfe homeostatic iron regulator gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:10381492 736272 Hfe homeostatic iron regulator gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:18249176 736272 Hfe homeostatic iron regulator gene MP:0008809 increased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:10557317 736272 Hfe homeostatic iron regulator gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:10557317 736272 Hfe homeostatic iron regulator gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:14618243 736272 Hfe homeostatic iron regulator gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:18249176 736272 Hfe homeostatic iron regulator gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:18316026 736272 Hfe homeostatic iron regulator gene MP:0008811 abnormal brain iron level IAGP N RGD:5509061 20141003 MGI PMID:23429074 736272 Hfe homeostatic iron regulator gene MP:0008811 abnormal brain iron level IAGP N RGD:5509061 20151112 MGI PMID:24439478 736272 Hfe homeostatic iron regulator gene MP:0008911 induced hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:16491649 736272 Hfe homeostatic iron regulator gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20180830 MGI PMID:20976594 736272 Hfe homeostatic iron regulator gene MP:0010161 decreased brain cholesterol level IAGP N RGD:5509061 20151112 MGI PMID:24439478 736272 Hfe homeostatic iron regulator gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20180830 MGI PMID:20976594 736272 Hfe homeostatic iron regulator gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20180830 MGI PMID:20976594 736272 Hfe homeostatic iron regulator gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20151112 MGI PMID:24439478 736272 Hfe homeostatic iron regulator gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20151112 MGI PMID:24439478 736272 Hfe homeostatic iron regulator gene MP:0020369 increased intestinal iron level IAGP N RGD:5509061 20161020 MGI PMID:10791995 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:3340629 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:3340629 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:11555633 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0000756 forelimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20141003 MGI PMID:3340629 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:8474599 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11555633 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11555633 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:18771733 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22355774 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:3340629 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20141003 MGI PMID:3340629 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11555633 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:3340629 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20170105 MGI 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18771733 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22355774 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11555633 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11555633 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18771733 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22355774 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:3340629 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0002229 neurodegeneration IEA N RGD:5509061 20111116 MGI 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20240523 MGI 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0003063 increased coping response IEA N RGD:5509061 20111116 MGI 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0003158 dysphagia IAGP N RGD:5509061 20141003 MGI PMID:11555633 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20141003 MGI PMID:11555633 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0003312 abnormal locomotor coordination IEA N RGD:5509061 20111116 MGI 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22355774 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20170105 MGI 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:11555633 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:20080621 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:3340629 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:8474599 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20240523 MGI 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20141003 MGI PMID:22355774 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:3340629 736277 Uchl1 ubiquitin carboxy-terminal hydrolase L1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:22355774 736282 Ccnc cyclin C gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20151217 MGI PMID:25344755 736282 Ccnc cyclin C gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20151217 MGI PMID:25344755 736282 Ccnc cyclin C gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20151217 MGI PMID:25344755 736282 Ccnc cyclin C gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20151217 MGI PMID:25344755 736282 Ccnc cyclin C gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20151217 MGI PMID:25344755 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220922 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000132 thickened long bone epiphysis IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000149 abnormal scapula morphology IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000150 abnormal rib morphology IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:12205031 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20220519 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000552 abnormal radius morphology IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000558 abnormal tibia morphology IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:12520522 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15102089 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20201022 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15102089 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0002187 abnormal fibula morphology IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:15102089 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0002764 short tibia IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:15102089 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:12674324 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:12689675 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0003112 enlarged parathyroid gland IAGP N RGD:5509061 20150305 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:12520522 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:15769857 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20220519 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0005108 abnormal ulna morphology IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0005296 abnormal humerus morphology IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0005298 abnormal clavicle morphology IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0009091 endometrium hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0009445 osteomalacia IAGP N RGD:5509061 20141003 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20160811 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160421 MGI 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:11416036 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:11416220 736283 Cyp27b1 cytochrome P450, family 27, subfamily b, polypeptide 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20160616 MGI PMID:12520522 736285 Chrna6 cholinergic receptor, nicotinic, alpha polypeptide 6 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:11850448 736286 Numb NUMB endocytic adaptor protein gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17174898 736286 Numb NUMB endocytic adaptor protein gene MP:0000822 abnormal brain ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0000823 abnormal lateral ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17174898 736286 Numb NUMB endocytic adaptor protein gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:14729486 736286 Numb NUMB endocytic adaptor protein gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:14729486 736286 Numb NUMB endocytic adaptor protein gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:14729486 736286 Numb NUMB endocytic adaptor protein gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14729486 736286 Numb NUMB endocytic adaptor protein gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:14729486 736286 Numb NUMB endocytic adaptor protein gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:14729486 736286 Numb NUMB endocytic adaptor protein gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:14729486 736286 Numb NUMB endocytic adaptor protein gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:14729486 736286 Numb NUMB endocytic adaptor protein gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:10841580 736286 Numb NUMB endocytic adaptor protein gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0000936 small embryonic telencephalon IAGP N RGD:5509061 20141003 MGI PMID:10841580 736286 Numb NUMB endocytic adaptor protein gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:14729486 736286 Numb NUMB endocytic adaptor protein gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10841580 736286 Numb NUMB endocytic adaptor protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12410312 736286 Numb NUMB endocytic adaptor protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17174898 736286 Numb NUMB endocytic adaptor protein gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12410312 736286 Numb NUMB endocytic adaptor protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10841580 736286 Numb NUMB endocytic adaptor protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12410312 736286 Numb NUMB endocytic adaptor protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0002645 abnormal intestinal cholesterol absorption IAGP N RGD:5509061 20151224 MGI PMID:24336247 736286 Numb NUMB endocytic adaptor protein gene MP:0002653 abnormal ependyma morphology IAGP N RGD:5509061 20141003 MGI PMID:17174898 736286 Numb NUMB endocytic adaptor protein gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17174898 736286 Numb NUMB endocytic adaptor protein gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:10841580 736286 Numb NUMB endocytic adaptor protein gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0004073 caudal body truncation IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0004188 delayed embryo turning IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12410312 736286 Numb NUMB endocytic adaptor protein gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17174898 736286 Numb NUMB endocytic adaptor protein gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:17174898 736286 Numb NUMB endocytic adaptor protein gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:12410312 736286 Numb NUMB endocytic adaptor protein gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20151224 MGI PMID:24336247 736286 Numb NUMB endocytic adaptor protein gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:14729486 736286 Numb NUMB endocytic adaptor protein gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:17174898 736286 Numb NUMB endocytic adaptor protein gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:14729486 736286 Numb NUMB endocytic adaptor protein gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:10841580 736286 Numb NUMB endocytic adaptor protein gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14729486 736286 Numb NUMB endocytic adaptor protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10841580 736286 Numb NUMB endocytic adaptor protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12410312 736286 Numb NUMB endocytic adaptor protein gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0011523 thin placenta labyrinth IAGP N RGD:5509061 20141003 MGI PMID:11412999 736286 Numb NUMB endocytic adaptor protein gene MP:0011724 ectopic cortical neuron IAGP N RGD:5509061 20141003 MGI PMID:14687546 736286 Numb NUMB endocytic adaptor protein gene MP:0012703 decreased embryonic neuroepithelium thickness IAGP N RGD:5509061 20141003 MGI PMID:12410312 736286 Numb NUMB endocytic adaptor protein gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:10841580 736286 Numb NUMB endocytic adaptor protein gene MP:0020527 small thalamus IAGP N RGD:5509061 20180208 MGI PMID:14687546 736292 Cdc5l cell division cycle 5-like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 736292 Cdc5l cell division cycle 5-like gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210520 MGI 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0000532 kidney vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15829709 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15829709 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:15829709 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:21849488 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:15123796 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:15829709 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:16055743 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:21849488 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:15829709 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15829709 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0005524 abnormal renal plasma flow rate IAGP N RGD:5509061 20141003 MGI PMID:15829709 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0005556 abnormal renal filtration rate IAGP N RGD:5509061 20141003 MGI PMID:21849488 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:21849488 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:15829709 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0011417 abnormal renal transport IAGP N RGD:5509061 20141003 MGI PMID:15123796 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0011417 abnormal renal transport IAGP N RGD:5509061 20141003 MGI PMID:15829709 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0011417 abnormal renal transport IAGP N RGD:5509061 20141003 MGI PMID:16055743 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0011431 increased urine flow rate IAGP N RGD:5509061 20141003 MGI PMID:15123796 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0011431 increased urine flow rate IAGP N RGD:5509061 20141003 MGI PMID:15829709 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0011466 increased urine urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:15829709 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:21849488 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0011741 increased urine nitrite level IAGP N RGD:5509061 20141003 MGI PMID:15829709 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:15829709 736297 Slc14a2 solute carrier family 14 (urea transporter), member 2 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:21849488 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12590258 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:17643102 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20160310 MGI PMID:22110743 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20160310 MGI PMID:22110743 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:20592216 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15314171 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15793579 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16791847 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17643102 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19596243 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20080941 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:12590258 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:12590258 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20210218 MGI PMID:17643102 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:20592216 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:21491498 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21491498 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:17643102 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:18760695 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:19596243 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:22302821 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20191003 MGI PMID:30672734 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:15314171 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:15793579 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:16791847 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:12590258 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17643102 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:19596243 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20592216 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:19596243 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20160310 MGI PMID:22110743 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001105 abnormal PNS glial cell morphology IAGP N RGD:5509061 20160310 MGI PMID:22110743 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20592216 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22302821 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22764250 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001107 decreased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:22302821 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:12590258 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15314171 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16791847 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:19185024 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:20371806 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001265 decreased body size IAGP N RGD:5509061 20160310 MGI PMID:22110743 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001270 distended abdomen IAGP N RGD:5509061 20160310 MGI PMID:22110743 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:20592216 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12590258 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15793579 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17643102 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20371806 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19185024 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21491498 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15793579 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19185024 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20371806 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21491498 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12590258 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:19185024 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:22302821 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:15793579 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:19185024 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:21491498 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15793579 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19185024 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20160310 MGI PMID:22110743 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17643102 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:15793579 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:20592216 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:17643102 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:19596243 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:19185024 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12590258 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15793579 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17643102 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20592216 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0002083 premature death IAGP N RGD:5509061 20160310 MGI PMID:22110743 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:12590258 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:17643102 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20160310 MGI PMID:22110743 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20592216 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20230914 MGI PMID:36378242 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0002731 megacolon IAGP N RGD:5509061 20141003 MGI PMID:20592216 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:21491498 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0002826 tonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20080941 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0003005 abnormal hippocampal fimbria morphology IAGP N RGD:5509061 20180628 MGI PMID:28836307 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0003354 astrocytosis IAGP N RGD:5509061 20180628 MGI PMID:28836307 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0003354 astrocytosis IAGP N RGD:5509061 20220908 MGI PMID:35274615 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17643102 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0003647 absent oligodendrocytes IAGP N RGD:5509061 20141003 MGI PMID:15314171 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0003647 absent oligodendrocytes IAGP N RGD:5509061 20141003 MGI PMID:16791847 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:20080941 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:20592216 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:22302821 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:22764250 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:19185024 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0005015 increased T cell number IAGP N RGD:5509061 20180628 MGI PMID:28836307 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0005238 increased brain size IAGP N RGD:5509061 20141003 MGI PMID:20592216 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23777740 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20180830 MGI PMID:27124591 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:17643102 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:19185024 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22302821 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20220908 MGI PMID:35274615 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:12590258 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:15314171 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:16791847 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0005405 axon degeneration IAGP N RGD:5509061 20160310 MGI PMID:22110743 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0005405 axon degeneration IAGP N RGD:5509061 20170629 MGI PMID:27504968 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0005405 axon degeneration IAGP N RGD:5509061 20220908 MGI PMID:35274615 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:17643102 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:20592216 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:19185024 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:22302821 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20170629 MGI PMID:27504968 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20191003 MGI PMID:30672734 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:17643102 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0008918 microgliosis IAGP N RGD:5509061 20180628 MGI PMID:28836307 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0008918 microgliosis IAGP N RGD:5509061 20220908 MGI PMID:35274615 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20160310 MGI PMID:22110743 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:15314171 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0009434 paraparesis IAGP N RGD:5509061 20141003 MGI PMID:16791847 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20180628 MGI PMID:28836307 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141003 MGI PMID:20592216 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0010050 hypermyelination IAGP N RGD:5509061 20141003 MGI PMID:22764250 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0010734 abnormal paranode morphology IAGP N RGD:5509061 20141003 MGI PMID:20371806 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0010735 abnormal paranodal axoglial junction morphology IAGP N RGD:5509061 20141003 MGI PMID:20371806 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0010738 abnormal internode morphology IAGP N RGD:5509061 20141003 MGI PMID:22302821 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0010739 abnormal axolemma morphology IAGP N RGD:5509061 20141003 MGI PMID:22302821 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0010742 increased Schwann cell number IAGP N RGD:5509061 20141003 MGI PMID:22764250 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20220908 MGI PMID:35274615 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15314171 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16791847 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18760695 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19185024 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19596243 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0011639 decreased mitochondrial DNA content IAGP N RGD:5509061 20160310 MGI PMID:22110743 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0012674 tomacula IAGP N RGD:5509061 20170629 MGI PMID:27504968 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0012674 tomacula IAGP N RGD:5509061 20191003 MGI PMID:30672734 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0013438 dysmyelination IAGP N RGD:5509061 20170629 MGI PMID:27504968 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:21491498 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:19185024 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0014387 decreased neuron mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:22110743 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0020380 abnormal galactolipid level IAGP N RGD:5509061 20190815 MGI PMID:21491498 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 736299 Cnp 2',3'-cyclic nucleotide 3' phosphodiesterase gene MP:0031204 hindlimb paresis IAGP N RGD:5509061 20210218 MGI PMID:17643102 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20180906 MGI PMID:29716523 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11133164 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10702423 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0000334 decreased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:9767409 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:17148658 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20150611 MGI PMID:17029217 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20150611 MGI PMID:18637146 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20150611 MGI PMID:17029217 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220707 MGI PMID:33507326 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0001260 increased body weight IAGP N RGD:5509061 20180906 MGI PMID:29716523 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0001358 aggression towards inanimate objects IAGP N RGD:5509061 20150226 MGI PMID:23118208 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0001388 abnormal stationary movement IAGP N RGD:5509061 20180906 MGI PMID:29716523 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20180906 MGI PMID:29716523 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20150611 MGI PMID:17029217 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20150611 MGI PMID:18637146 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:18202191 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:16723706 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20150611 MGI PMID:18637146 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:16723706 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18202191 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:18202187 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220707 MGI PMID:33507326 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16723706 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18202191 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002436 abnormal CD8-positive, alpha-beta cytotoxic T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16723706 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:10702423 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10702423 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18250477 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16723706 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20150226 MGI PMID:23118208 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002620 abnormal monocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10702423 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20150611 MGI PMID:17029217 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20150611 MGI PMID:18637146 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20220707 MGI PMID:33507326 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20150611 MGI PMID:17029217 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20150611 MGI PMID:17029217 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:11133164 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20220707 MGI PMID:33507326 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:10702423 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20150702 MGI PMID:16723706 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0003331 increased hepatocellular carcinoma incidence IAGP N RGD:5509061 20150611 MGI PMID:18637146 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20150611 MGI PMID:18637146 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11133164 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20150611 MGI PMID:17029217 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:17148658 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:18250477 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:10702423 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:16723706 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20220707 MGI PMID:33507326 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:17148658 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20220707 MGI PMID:33507326 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220707 MGI PMID:33507326 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220707 MGI PMID:33507326 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220707 MGI PMID:33507326 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20230504 MGI PMID:36062328 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10702423 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10702423 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:16723706 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:16723706 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0005044 sepsis IAGP N RGD:5509061 20141003 MGI PMID:18202191 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:18202187 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18156214 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0005341 decreased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:18156214 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20141003 MGI PMID:16723706 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0008560 increased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:18202191 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0008669 increased interleukin-12b secretion IAGP N RGD:5509061 20141003 MGI PMID:16723706 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:18202191 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:18202191 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20230504 MGI PMID:36062328 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20150611 MGI PMID:17029217 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20150226 MGI PMID:23118208 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18202191 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20180906 MGI PMID:29716523 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20230504 MGI PMID:36062328 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20230504 MGI PMID:36062328 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20230504 MGI PMID:36062328 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20230504 MGI PMID:36062328 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0010932 increased trabecular bone connectivity density IAGP N RGD:5509061 20230504 MGI PMID:36062328 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0010964 increased compact bone volume IAGP N RGD:5509061 20230504 MGI PMID:36062328 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0011080 increased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10702423 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0013615 increased volumetric bone mineral density IAGP N RGD:5509061 20230504 MGI PMID:36062328 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0013620 increased internal diameter of femur IAGP N RGD:5509061 20230504 MGI PMID:36062328 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20230504 MGI PMID:36062328 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0014045 Mallory bodies IAGP N RGD:5509061 20160304 MGI PMID:17029217 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220707 MGI PMID:33507326 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20180906 MGI PMID:29716523 736305 Lgals3 lectin, galactose binding, soluble 3 gene MP:0021187 increased bone mineral density of vertebrae IAGP N RGD:5509061 20230504 MGI PMID:36062328 736310 Nup50 nucleoporin 50 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10891500 736310 Nup50 nucleoporin 50 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:10891500 736310 Nup50 nucleoporin 50 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:10891500 736310 Nup50 nucleoporin 50 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10891500 736312 Syt5 synaptotagmin V gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 736312 Syt5 synaptotagmin V gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17521570 736312 Syt5 synaptotagmin V gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17521570 736314 Pccb propionyl Coenzyme A carboxylase, beta polypeptide gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 736314 Pccb propionyl Coenzyme A carboxylase, beta polypeptide gene MP:0000562 polydactyly IEA N RGD:5509061 20230601 MGI 736314 Pccb propionyl Coenzyme A carboxylase, beta polypeptide gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 736314 Pccb propionyl Coenzyme A carboxylase, beta polypeptide gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 736314 Pccb propionyl Coenzyme A carboxylase, beta polypeptide gene MP:0001297 microphthalmia IEA N RGD:5509061 20230601 MGI 736314 Pccb propionyl Coenzyme A carboxylase, beta polypeptide gene MP:0001914 hemorrhage IEA N RGD:5509061 20230601 MGI 736314 Pccb propionyl Coenzyme A carboxylase, beta polypeptide gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 736314 Pccb propionyl Coenzyme A carboxylase, beta polypeptide gene MP:0003054 spina bifida IEA N RGD:5509061 20230601 MGI 736314 Pccb propionyl Coenzyme A carboxylase, beta polypeptide gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210128 MGI 736314 Pccb propionyl Coenzyme A carboxylase, beta polypeptide gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736316 St6gal1 beta galactoside alpha 2,6 sialyltransferase 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16849643 736316 St6gal1 beta galactoside alpha 2,6 sialyltransferase 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16849643 736316 St6gal1 beta galactoside alpha 2,6 sialyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9539767 736316 St6gal1 beta galactoside alpha 2,6 sialyltransferase 1 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18354178 736316 St6gal1 beta galactoside alpha 2,6 sialyltransferase 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12672700 736316 St6gal1 beta galactoside alpha 2,6 sialyltransferase 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:12672700 736316 St6gal1 beta galactoside alpha 2,6 sialyltransferase 1 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:16849643 736316 St6gal1 beta galactoside alpha 2,6 sialyltransferase 1 gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20141003 MGI PMID:16849643 736316 St6gal1 beta galactoside alpha 2,6 sialyltransferase 1 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18354178 736316 St6gal1 beta galactoside alpha 2,6 sialyltransferase 1 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:18354178 736320 Ptprq protein tyrosine phosphatase receptor type Q gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:14534255 736320 Ptprq protein tyrosine phosphatase receptor type Q gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:14534255 736320 Ptprq protein tyrosine phosphatase receptor type Q gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:14534255 736320 Ptprq protein tyrosine phosphatase receptor type Q gene MP:0004431 abnormal hair cell mechanoelectric transduction IAGP N RGD:5509061 20141003 MGI PMID:14534255 736320 Ptprq protein tyrosine phosphatase receptor type Q gene MP:0004492 abnormal orientation of inner hair cell stereociliary bundles IAGP N RGD:5509061 20141003 MGI PMID:14534255 736320 Ptprq protein tyrosine phosphatase receptor type Q gene MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:14534255 736320 Ptprq protein tyrosine phosphatase receptor type Q gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:14534255 736320 Ptprq protein tyrosine phosphatase receptor type Q gene MP:0004527 abnormal outer hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:14534255 736320 Ptprq protein tyrosine phosphatase receptor type Q gene MP:0004531 short outer hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:14534255 736320 Ptprq protein tyrosine phosphatase receptor type Q gene MP:0004532 abnormal inner hair cell stereociliary bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:14534255 736320 Ptprq protein tyrosine phosphatase receptor type Q gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:14534255 736320 Ptprq protein tyrosine phosphatase receptor type Q gene MP:0004534 decreased inner hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:14534255 736320 Ptprq protein tyrosine phosphatase receptor type Q gene MP:0004585 absent vestibular hair bundle shaft connectors IAGP N RGD:5509061 20141003 MGI PMID:14534255 736320 Ptprq protein tyrosine phosphatase receptor type Q gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20160929 MGI PMID:27534441 736320 Ptprq protein tyrosine phosphatase receptor type Q gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:14534255 736323 Actr3 ARP3 actin-related protein 3 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:18035060 736323 Actr3 ARP3 actin-related protein 3 gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:18035060 736323 Actr3 ARP3 actin-related protein 3 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:18035060 736323 Actr3 ARP3 actin-related protein 3 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18035060 736326 Jtb jumping translocation breakpoint gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20201231 MGI 736326 Jtb jumping translocation breakpoint gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736326 Jtb jumping translocation breakpoint gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20191128 MGI 736326 Jtb jumping translocation breakpoint gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 736332 Maged1 MAGE family member D1 gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:18772898 736332 Maged1 MAGE family member D1 gene MP:0001361 social withdrawal IAGP N RGD:5509061 20141003 MGI PMID:22457503 736332 Maged1 MAGE family member D1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22457503 736332 Maged1 MAGE family member D1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:22457503 736332 Maged1 MAGE family member D1 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:22457503 736332 Maged1 MAGE family member D1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20231207 MGI 736332 Maged1 MAGE family member D1 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18772898 736332 Maged1 MAGE family member D1 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:20133718 736332 Maged1 MAGE family member D1 gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:22457503 736332 Maged1 MAGE family member D1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210826 MGI 736332 Maged1 MAGE family member D1 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:20133718 736332 Maged1 MAGE family member D1 gene MP:0008859 abnormal hair cycle catagen phase IAGP N RGD:5509061 20141003 MGI PMID:18772898 736332 Maged1 MAGE family member D1 gene MP:0009253 abnormal sympathetic neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18772898 736332 Maged1 MAGE family member D1 gene MP:0009710 anhedonia IAGP N RGD:5509061 20141003 MGI PMID:22457503 736332 Maged1 MAGE family member D1 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:22457503 736332 Maged1 MAGE family member D1 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:22457503 736332 Maged1 MAGE family member D1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20210520 MGI 736332 Maged1 MAGE family member D1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20211021 MGI 736332 Maged1 MAGE family member D1 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:20300063 736332 Maged1 MAGE family member D1 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:20300063 736332 Maged1 MAGE family member D1 gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:20300063 736335 Mstn myostatin gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0000520 absent kidney IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:12704695 736335 Mstn myostatin gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:22318951 736335 Mstn myostatin gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20170629 MGI PMID:26769954 736335 Mstn myostatin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11855847 736335 Mstn myostatin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12717734 736335 Mstn myostatin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:16219664 736335 Mstn myostatin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22318951 736335 Mstn myostatin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:9335610 736335 Mstn myostatin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16219664 736335 Mstn myostatin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20810712 736335 Mstn myostatin gene MP:0001264 increased body size IAGP N RGD:5509061 20141003 MGI PMID:9139826 736335 Mstn myostatin gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:11855847 736335 Mstn myostatin gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:9139826 736335 Mstn myostatin gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:16219664 736335 Mstn myostatin gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:22318951 736335 Mstn myostatin gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12717734 736335 Mstn myostatin gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9335610 736335 Mstn myostatin gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17592022 736335 Mstn myostatin gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17267614 736335 Mstn myostatin gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:12704695 736335 Mstn myostatin gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0003397 increased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:12717734 736335 Mstn myostatin gene MP:0003397 increased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:16219664 736335 Mstn myostatin gene MP:0003397 increased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:9139826 736335 Mstn myostatin gene MP:0003398 increased skeletal muscle size IAGP N RGD:5509061 20141003 MGI PMID:11855847 736335 Mstn myostatin gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:11855847 736335 Mstn myostatin gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22318951 736335 Mstn myostatin gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:11855847 736335 Mstn myostatin gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20170629 MGI PMID:26769954 736335 Mstn myostatin gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:12704695 736335 Mstn myostatin gene MP:0004508 abnormal pectoral girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0004627 abnormal trochanter morphology IAGP N RGD:5509061 20141003 MGI PMID:12704695 736335 Mstn myostatin gene MP:0004645 decreased vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0004650 increased lumbar vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0004651 increased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0004656 absent sacral vertebrae IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:17148752 736335 Mstn myostatin gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:17267614 736335 Mstn myostatin gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:18286185 736335 Mstn myostatin gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:9139826 736335 Mstn myostatin gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:9335610 736335 Mstn myostatin gene MP:0004893 decreased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:22318951 736335 Mstn myostatin gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0005451 abnormal body composition IAGP N RGD:5509061 20141003 MGI PMID:9335610 736335 Mstn myostatin gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11855847 736335 Mstn myostatin gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0008552 abnormal circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11855847 736335 Mstn myostatin gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11855847 736335 Mstn myostatin gene MP:0009301 decreased parametrial fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11855847 736335 Mstn myostatin gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11855847 736335 Mstn myostatin gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:12717734 736335 Mstn myostatin gene MP:0009399 increased skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:9139826 736335 Mstn myostatin gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:17148752 736335 Mstn myostatin gene MP:0009401 increased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:18286185 736335 Mstn myostatin gene MP:0009405 increased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:18286185 736335 Mstn myostatin gene MP:0009405 increased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0009405 increased skeletal muscle fiber number IAGP N RGD:5509061 20141003 MGI PMID:9139826 736335 Mstn myostatin gene MP:0009421 increased gastrocnemius weight IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0009459 skeletal muscle hyperplasia IAGP N RGD:5509061 20170629 MGI PMID:26769954 736335 Mstn myostatin gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12717734 736335 Mstn myostatin gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:22318951 736335 Mstn myostatin gene MP:0009461 skeletal muscle hypertrophy IAGP N RGD:5509061 20170629 MGI PMID:26769954 736335 Mstn myostatin gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11855847 736335 Mstn myostatin gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:12704695 736335 Mstn myostatin gene MP:0010226 increased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:12704695 736335 Mstn myostatin gene MP:0010226 increased quadriceps weight IAGP N RGD:5509061 20141003 MGI PMID:19208906 736335 Mstn myostatin gene MP:0010238 increased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:22318951 736335 Mstn myostatin gene MP:0010238 increased skeletal muscle weight IAGP N RGD:5509061 20170629 MGI PMID:26769954 736335 Mstn myostatin gene MP:0010239 decreased skeletal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:20810712 736335 Mstn myostatin gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19298661 736335 Mstn myostatin gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:11855847 736335 Mstn myostatin gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:19298661 736335 Mstn myostatin gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:12704695 736335 Mstn myostatin gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:19208906 736337 Agxt alanine-glyoxylate aminotransferase gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:17110443 736337 Agxt alanine-glyoxylate aminotransferase gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:22189945 736337 Agxt alanine-glyoxylate aminotransferase gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:17110443 736337 Agxt alanine-glyoxylate aminotransferase gene MP:0005360 urolithiasis IAGP N RGD:5509061 20141003 MGI PMID:17110443 736337 Agxt alanine-glyoxylate aminotransferase gene MP:0005558 decreased creatinine clearance IAGP N RGD:5509061 20141003 MGI PMID:17110443 736337 Agxt alanine-glyoxylate aminotransferase gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22189945 736337 Agxt alanine-glyoxylate aminotransferase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20201210 MGI PMID:31821850 736337 Agxt alanine-glyoxylate aminotransferase gene MP:0009645 crystalluria IAGP N RGD:5509061 20141003 MGI PMID:17110443 736337 Agxt alanine-glyoxylate aminotransferase gene MP:0011517 hyperoxaluria IAGP N RGD:5509061 20141003 MGI PMID:17110443 736337 Agxt alanine-glyoxylate aminotransferase gene MP:0011517 hyperoxaluria IAGP N RGD:5509061 20201210 MGI PMID:31821850 736341 Pnoc prepronociceptin gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20141003 MGI PMID:16519664 736341 Pnoc prepronociceptin gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:11311544 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0000154 rib fusion IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16864769 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:16864769 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:16864769 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:16864769 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16864769 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0004096 abnormal midbrain-hindbrain boundary development IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0004388 absent prechordal plate IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:16864769 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16864769 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0011259 abnormal cephalic neural fold morphology IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:16864769 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:16864769 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:16864769 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0012176 abnormal head development IAGP N RGD:5509061 20141003 MGI PMID:16864769 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0012283 decreased sternebra number IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0012517 absent diencephalon IAGP N RGD:5509061 20141003 MGI PMID:15857913 736343 Ssbp3 single-stranded DNA binding protein 3 gene MP:0030324 abnormal anterior head development IAGP N RGD:5509061 20171109 MGI PMID:15857913 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20201022 MGI 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201231 MGI 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0001513 limb grasping IEA N RGD:5509061 20201022 MGI 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9192619 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:16905251 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20170330 MGI PMID:24456331 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0002083 premature death IAGP N RGD:5509061 20170330 MGI PMID:24456331 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0002164 abnormal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:9192619 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20170330 MGI PMID:24456331 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20170330 MGI PMID:24456331 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0002711 decreased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:9192619 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0002711 decreased glucagon secretion IAGP N RGD:5509061 20170330 MGI PMID:24456331 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9192619 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12697744 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:9192619 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:9192619 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0003365 increased glucagonoma incidence IAGP N RGD:5509061 20170330 MGI PMID:26261055 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0003430 increased pancreatic islet cell adenoma incidence IAGP N RGD:5509061 20170330 MGI PMID:24456331 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0003972 decreased pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:12697744 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0004270 analgesia IAGP N RGD:5509061 20141003 MGI PMID:16905251 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20210128 MGI 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:9192619 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20170330 MGI PMID:24456331 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20170330 MGI PMID:24456331 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:9192619 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20170330 MGI PMID:24456331 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:16905251 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:9192619 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20210128 MGI 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0008953 abnormal pancreatic somatostatin secretion IAGP N RGD:5509061 20141003 MGI PMID:9192619 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20170330 MGI PMID:24456331 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20170330 MGI PMID:24456331 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20170330 MGI PMID:24456331 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12933680 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20170330 MGI PMID:24456331 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0009179 abnormal pancreatic alpha cell differentiation IAGP N RGD:5509061 20170330 MGI PMID:24456331 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0009180 increased pancreatic delta cell number IAGP N RGD:5509061 20141003 MGI PMID:9192619 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0014109 increased pancreatic alpha cell proliferation IAGP N RGD:5509061 20180614 MGI PMID:12933680 736346 Pcsk2 proprotein convertase subtilisin/kexin type 2 gene MP:0030589 increased pancreatic alpha cell mass IAGP N RGD:5509061 20180614 MGI PMID:9192619 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:14985257 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0001523 impaired righting response IEA N RGD:5509061 20181227 MGI 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:14985257 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:14985257 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:14985257 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24445777 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:14985257 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0002718 abnormal inner cell mass morphology IAGP N RGD:5509061 20141003 MGI PMID:14985257 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:14985257 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20220519 MGI 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14985257 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:14985257 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0011193 embryonic epiblast cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:14985257 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20211021 MGI 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0012113 decreased inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:14985257 736347 Serpinb5 serine (or cysteine) peptidase inhibitor, clade B, member 5 gene MP:0012114 absent inner cell mass proliferation IAGP N RGD:5509061 20141003 MGI PMID:14985257 736351 Slco1a1 solute carrier organic anion transporter family, member 1a1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21561886 736351 Slco1a1 solute carrier organic anion transporter family, member 1a1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21561886 736351 Slco1a1 solute carrier organic anion transporter family, member 1a1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:21561886 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0001850 increased susceptibility to otitis media IAGP N RGD:5509061 20141003 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0001872 sinus inflammation IAGP N RGD:5509061 20141003 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:20550699 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20550699 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0001950 abnormal respiratory sounds IAGP N RGD:5509061 20141003 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:20550699 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:17078042 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:20550699 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:20550699 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:20550699 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:20550699 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0009838 abnormal sperm axoneme morphology IAGP N RGD:5509061 20141003 MGI PMID:20550699 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0010752 impaired mucociliary clearance IAGP N RGD:5509061 20141003 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0011053 decreased respiratory motile cilia number IAGP N RGD:5509061 20141003 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0011055 abnormal respiratory motile cilium physiology IAGP N RGD:5509061 20141003 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0011056 abnormal brain ependyma motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0011082 abnormal gastrointestinal motility IAGP N RGD:5509061 20141003 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17078042 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0011644 abnormal oviduct epithelium motile cilium morphology IAGP N RGD:5509061 20141003 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0011998 decreased embryonic cilium length IAGP N RGD:5509061 20190725 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0013202 abnormal cilium morphology IAGP N RGD:5509061 20230615 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0030966 decreased brain ependyma motile cilium number IAGP N RGD:5509061 20190725 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0031088 coughing IAGP N RGD:5509061 20210211 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0031089 sneezing IAGP N RGD:5509061 20210211 MGI PMID:22265411 736352 Odf2 outer dense fiber of sperm tails 2 gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220317 MGI PMID:20550699 736354 Slc29a2 solute carrier family 29 (nucleoside transporters), member 2 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20180503 MGI PMID:23603835 736354 Slc29a2 solute carrier family 29 (nucleoside transporters), member 2 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20180503 MGI PMID:23603835 736356 Mpeg1 macrophage expressed gene 1 gene MP:0009785 abnormal susceptibility to infection induced morbidity/mortality IAGP N RGD:5509061 20190314 MGI PMID:26418746 736358 Cxxc4 CXXC finger 4 gene MP:0001399 hyperactivity IEA N RGD:5509061 20181227 MGI 736358 Cxxc4 CXXC finger 4 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20240314 MGI PMID:35390758 736358 Cxxc4 CXXC finger 4 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20220811 MGI 736358 Cxxc4 CXXC finger 4 gene MP:0008957 abnormal placenta junctional zone morphology IAGP N RGD:5509061 20240314 MGI PMID:35390758 736358 Cxxc4 CXXC finger 4 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20240523 MGI 736358 Cxxc4 CXXC finger 4 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 736358 Cxxc4 CXXC finger 4 gene MP:0011519 abnormal placenta labyrinth size IAGP N RGD:5509061 20240314 MGI PMID:35390758 736358 Cxxc4 CXXC finger 4 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210128 MGI 736362 Prkcz protein kinase C, zeta gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:11684013 736362 Prkcz protein kinase C, zeta gene MP:0001289 persistence of hyaloid vascular system IAGP N RGD:5509061 20160922 MGI PMID:24652767 736362 Prkcz protein kinase C, zeta gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:23283171 736362 Prkcz protein kinase C, zeta gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20190124 MGI PMID:25340873 736362 Prkcz protein kinase C, zeta gene MP:0002362 abnormal spleen marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:11684013 736362 Prkcz protein kinase C, zeta gene MP:0002389 abnormal Peyer's patch follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11684013 736362 Prkcz protein kinase C, zeta gene MP:0002877 abnormal melanocyte morphology IAGP N RGD:5509061 20160922 MGI PMID:24652767 736362 Prkcz protein kinase C, zeta gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20160804 MGI 736362 Prkcz protein kinase C, zeta gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20160922 MGI PMID:24652767 736362 Prkcz protein kinase C, zeta gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:11684013 736362 Prkcz protein kinase C, zeta gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20160804 MGI 736362 Prkcz protein kinase C, zeta gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:11684013 736362 Prkcz protein kinase C, zeta gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20160804 MGI 736362 Prkcz protein kinase C, zeta gene MP:0014348 decreased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:11684013 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:12122007 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:12122007 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:12122007 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:12122007 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12122007 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:12122007 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12122007 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12122007 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:12122007 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0003653 decreased skin turgor IAGP N RGD:5509061 20141003 MGI PMID:12122007 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:12122007 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0005633 increased circulating sodium level IAGP N RGD:5509061 20141003 MGI PMID:12122007 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12122007 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12122007 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0011296 decreased tubuloglomerular feedback response IAGP N RGD:5509061 20141003 MGI PMID:12122007 736363 Kcnj1 potassium inwardly-rectifying channel, subfamily J, member 1 gene MP:0012551 metabolic acidosis IAGP N RGD:5509061 20170921 MGI PMID:12122007 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16123346 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23266956 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:19619492 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:19619492 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0000470 abnormal stomach morphology IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0000497 abnormal small intestine placement IAGP N RGD:5509061 20141003 MGI PMID:7935793 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0001199 thin skin IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11912494 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7935793 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:11912494 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:19487809 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:11912494 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:9637677 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:12697734 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:18155690 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:19619492 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0002083 premature death IAGP N RGD:5509061 20190131 MGI PMID:28934293 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16794995 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18155690 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0002710 increased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:11781323 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0002710 increased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:16123346 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15562255 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18155690 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19487809 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11912494 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:11781323 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:11912494 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:12697734 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15562255 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:16123346 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:20811152 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003335 exocrine pancreatic insufficiency IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:23266956 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003337 exocrine pancreas hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19619492 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:18155690 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:20811152 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:23382704 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:9637677 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11781323 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20811152 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9637677 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003655 absent pancreas IAGP N RGD:5509061 20141003 MGI PMID:16126192 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003655 absent pancreas IAGP N RGD:5509061 20141003 MGI PMID:7935793 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003655 absent pancreas IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:12221286 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:16126192 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:18394599 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:19487809 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:19619492 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0003934 abnormal pancreas development IAGP N RGD:5509061 20141003 MGI PMID:8625829 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0004141 abnormal enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:19487809 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:19619492 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:12697734 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:18394599 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:23382704 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:9637677 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16123346 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20811152 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005218 abnormal pancreatic delta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19487809 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20811152 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11781323 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:11912494 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12221286 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12697734 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15562255 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16123346 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16126192 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18155690 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19487809 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:20811152 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:9637677 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15562255 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005493 stomach epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19619492 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12221286 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12697734 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15562255 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18155690 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20811152 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:7935793 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:9637677 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16123346 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:11781323 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009109 decreased pancreas weight IAGP N RGD:5509061 20141003 MGI PMID:19487809 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009111 pancreas hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19487809 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:19487809 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20180614 MGI PMID:12697734 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009114 decreased pancreatic beta cell mass IAGP N RGD:5509061 20180614 MGI PMID:15372107 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009143 abnormal pancreatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009151 increased pancreatic ductal adenocarcinoma incidence IAGP N RGD:5509061 20190131 MGI PMID:28934293 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009152 increased pancreatic intraepithelial neoplasia incidence IAGP N RGD:5509061 20190131 MGI PMID:28934293 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009154 pancreatic acinar hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19619492 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009165 abnormal endocrine pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:19619492 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009168 decreased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:12697734 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009169 pancreatic islet hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19487809 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009170 abnormal pancreatic islet size IAGP N RGD:5509061 20141003 MGI PMID:20811152 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:12697734 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:16123346 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:20811152 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:18155690 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:23382704 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:9637677 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009180 increased pancreatic delta cell number IAGP N RGD:5509061 20141003 MGI PMID:18155690 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009184 abnormal PP cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19487809 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009185 increased PP cell number IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009189 abnormal pancreatic epsilon cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19487809 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:11912494 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:18155690 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:20811152 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009254 disorganized pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:9637677 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009488 abnormal pancreatic islet cell apoptosis IAGP N RGD:5509061 20180614 MGI PMID:12697734 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009511 distended stomach IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0009861 abnormal pyloric sphincter morphology IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0010785 abnormal stomach pyloric region morphology IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0010803 abnormal stomach enteroendocrine cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20141003 MGI PMID:11781323 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16418487 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7935793 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0011820 decreased pancreatic beta cell proliferation IAGP N RGD:5509061 20180614 MGI PMID:18155690 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0011911 abnormal pancreatic endocrine progenitor cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19487809 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0012520 absent Brunner's glands IAGP N RGD:5509061 20141003 MGI PMID:8631275 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0014109 increased pancreatic alpha cell proliferation IAGP N RGD:5509061 20180614 MGI PMID:18155690 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0014116 abnormal pancreatic beta cell apoptosis IAGP N RGD:5509061 20180614 MGI PMID:12697734 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0014117 increased pancreatic beta cell apoptosis IAGP N RGD:5509061 20160324 MGI PMID:20811152 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0014125 decreased amylin secretion IAGP N RGD:5509061 20160324 MGI PMID:11781323 736368 Pdx1 pancreatic and duodenal homeobox 1 gene MP:0030588 decreased pancreatic alpha cell mass IAGP N RGD:5509061 20180614 MGI PMID:19487809 736373 Slc6a20b solute carrier family 6 (neurotransmitter transporter), member 20B gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20240523 MGI 736373 Slc6a20b solute carrier family 6 (neurotransmitter transporter), member 20B gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 736373 Slc6a20b solute carrier family 6 (neurotransmitter transporter), member 20B gene MP:0002833 increased heart weight IEA N RGD:5509061 20240523 MGI 736373 Slc6a20b solute carrier family 6 (neurotransmitter transporter), member 20B gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 736373 Slc6a20b solute carrier family 6 (neurotransmitter transporter), member 20B gene MP:0005544 cornea deposits IEA N RGD:5509061 20240523 MGI 736373 Slc6a20b solute carrier family 6 (neurotransmitter transporter), member 20B gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 736373 Slc6a20b solute carrier family 6 (neurotransmitter transporter), member 20B gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20240523 MGI 736376 Aqp7 aquaporin 7 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:15591341 736376 Aqp7 aquaporin 7 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:15746100 736376 Aqp7 aquaporin 7 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:15998844 736376 Aqp7 aquaporin 7 gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20141003 MGI PMID:15998844 736376 Aqp7 aquaporin 7 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:15998844 736376 Aqp7 aquaporin 7 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17576812 736376 Aqp7 aquaporin 7 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:15998844 736376 Aqp7 aquaporin 7 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:15998844 736376 Aqp7 aquaporin 7 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17576812 736376 Aqp7 aquaporin 7 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:17576812 736376 Aqp7 aquaporin 7 gene MP:0003441 increased glycerol level IAGP N RGD:5509061 20141003 MGI PMID:15591341 736376 Aqp7 aquaporin 7 gene MP:0003441 increased glycerol level IAGP N RGD:5509061 20141003 MGI PMID:17576812 736376 Aqp7 aquaporin 7 gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:15591341 736376 Aqp7 aquaporin 7 gene MP:0003927 increased cellular glucose import IAGP N RGD:5509061 20141003 MGI PMID:17576812 736376 Aqp7 aquaporin 7 gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:18829704 736376 Aqp7 aquaporin 7 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:17576812 736376 Aqp7 aquaporin 7 gene MP:0005670 abnormal white adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:15746100 736376 Aqp7 aquaporin 7 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:15746100 736376 Aqp7 aquaporin 7 gene MP:0009172 small pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:17576812 736376 Aqp7 aquaporin 7 gene MP:0009177 decreased pancreatic alpha cell number IAGP N RGD:5509061 20141003 MGI PMID:17576812 736376 Aqp7 aquaporin 7 gene MP:0009186 decreased PP cell number IAGP N RGD:5509061 20141003 MGI PMID:17576812 736376 Aqp7 aquaporin 7 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:15746100 736376 Aqp7 aquaporin 7 gene MP:0030781 decreased urine glycerol level IAGP N RGD:5509061 20181004 MGI PMID:17077387 736377 Decr1 2,4-dienoyl CoA reductase 1, mitochondrial gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:19578400 736377 Decr1 2,4-dienoyl CoA reductase 1, mitochondrial gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19578400 736377 Decr1 2,4-dienoyl CoA reductase 1, mitochondrial gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19578400 736377 Decr1 2,4-dienoyl CoA reductase 1, mitochondrial gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19578400 736377 Decr1 2,4-dienoyl CoA reductase 1, mitochondrial gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:19578400 736377 Decr1 2,4-dienoyl CoA reductase 1, mitochondrial gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19578400 736377 Decr1 2,4-dienoyl CoA reductase 1, mitochondrial gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19578400 736377 Decr1 2,4-dienoyl CoA reductase 1, mitochondrial gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:19578400 736377 Decr1 2,4-dienoyl CoA reductase 1, mitochondrial gene MP:0031116 microvesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:19578400 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:16880535 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:19074029 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:19074029 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:19074029 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19074029 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:19074029 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:19074029 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:19074029 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19074029 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:19074029 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16880535 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19074029 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10600543 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:16880535 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:16880535 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0002238 abnormal nasal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:16880535 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:16880535 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:16880535 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0002762 ectopic cerebellar granule cells IAGP N RGD:5509061 20141003 MGI PMID:19074029 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16880535 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:16880535 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16880535 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:19074029 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0008439 abnormal cortical plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19074029 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19074029 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:16880535 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:16880535 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19074029 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16880535 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16880535 736381 Crk v-crk avian sarcoma virus CT10 oncogene homolog gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:16880535 736382 Areg amphiregulin gene MP:0000410 waved hair IAGP N RGD:5509061 20141003 MGI PMID:10331984 736382 Areg amphiregulin gene MP:0000410 waved hair IAGP N RGD:5509061 20150528 MGI PMID:12573256 736382 Areg amphiregulin gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:10331984 736382 Areg amphiregulin gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:11438495 736382 Areg amphiregulin gene MP:0000662 abnormal branching of the mammary ductal tree IAGP N RGD:5509061 20141003 MGI PMID:10331984 736382 Areg amphiregulin gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:10331984 736382 Areg amphiregulin gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:10331984 736382 Areg amphiregulin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11438495 736382 Areg amphiregulin gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:10331984 736382 Areg amphiregulin gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20141003 MGI PMID:10331984 736382 Areg amphiregulin gene MP:0001274 curly vibrissae IAGP N RGD:5509061 20150528 MGI PMID:12573256 736382 Areg amphiregulin gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10331984 736382 Areg amphiregulin gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:10331984 736382 Areg amphiregulin gene MP:0001314 cornea opacity IAGP N RGD:5509061 20141003 MGI PMID:10331984 736382 Areg amphiregulin gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 736382 Areg amphiregulin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10331984 736382 Areg amphiregulin gene MP:0002580 duodenal lesions IAGP N RGD:5509061 20141003 MGI PMID:11438495 736382 Areg amphiregulin gene MP:0002581 abnormal ileum morphology IAGP N RGD:5509061 20141003 MGI PMID:11438495 736382 Areg amphiregulin gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20170105 MGI 736382 Areg amphiregulin gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11438495 736382 Areg amphiregulin gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:11438495 736382 Areg amphiregulin gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:10331984 736382 Areg amphiregulin gene MP:0011015 decreased body surface temperature IAGP N RGD:5509061 20161124 MGI PMID:26317471 736382 Areg amphiregulin gene MP:0013716 hypolactation IAGP N RGD:5509061 20150402 MGI PMID:10331984 736382 Areg amphiregulin gene MP:0020946 increased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:26317471 736382 Areg amphiregulin gene MP:0031068 decreased blood oxygen saturation level IAGP N RGD:5509061 20200618 MGI PMID:26317471 736384 Glrx glutaredoxin gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:18586881 736384 Glrx glutaredoxin gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:18586881 736384 Glrx glutaredoxin gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18586881 736384 Glrx glutaredoxin gene MP:0003950 abnormal plasma membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:18586881 736384 Glrx glutaredoxin gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18586881 736384 Glrx glutaredoxin gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:17893043 736384 Glrx glutaredoxin gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:17893043 736386 Strn striatin, calmodulin binding protein gene MP:0002666 increased circulating aldosterone level IAGP N RGD:5509061 20161103 MGI PMID:25368024 736386 Strn striatin, calmodulin binding protein gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20161103 MGI PMID:25368024 736386 Strn striatin, calmodulin binding protein gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20161103 MGI PMID:25368024 736391 Ppbp pro-platelet basic protein gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 736391 Ppbp pro-platelet basic protein gene MP:0002442 abnormal leukocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23550035 736391 Ppbp pro-platelet basic protein gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:23550035 736391 Ppbp pro-platelet basic protein gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 736391 Ppbp pro-platelet basic protein gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 736391 Ppbp pro-platelet basic protein gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:23550035 736391 Ppbp pro-platelet basic protein gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20231207 MGI 736394 Ppat phosphoribosyl pyrophosphate amidotransferase gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20230119 MGI 736394 Ppat phosphoribosyl pyrophosphate amidotransferase gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20230119 MGI 736394 Ppat phosphoribosyl pyrophosphate amidotransferase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230119 MGI 736394 Ppat phosphoribosyl pyrophosphate amidotransferase gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 736394 Ppat phosphoribosyl pyrophosphate amidotransferase gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20230119 MGI 736394 Ppat phosphoribosyl pyrophosphate amidotransferase gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 736394 Ppat phosphoribosyl pyrophosphate amidotransferase gene MP:0005641 increased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20230119 MGI 736394 Ppat phosphoribosyl pyrophosphate amidotransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 736394 Ppat phosphoribosyl pyrophosphate amidotransferase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230119 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0000194 increased circulating calcium level IEA N RGD:5509061 20201022 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0003884 decreased macrophage cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0004609 vertebral fusion IEA N RGD:5509061 20150430 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20150430 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210128 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0005505 thrombocytosis IEA N RGD:5509061 20211021 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210128 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0008045 decreased NK cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20201022 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0008097 increased plasma cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0009926 decreased transitional stage T2 B cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20190124 MGI PMID:25340873 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20210128 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0010206 pigment incontinence IAGP N RGD:5509061 20190124 MGI PMID:25340873 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0010835 increased CD4-positive, alpha-beta memory T cell number IEA N RGD:5509061 20201022 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0012768 decreased KLRG1-positive NK cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0013157 increased KLRG1+ CD4 alpha-beta T cell number IEA N RGD:5509061 20201022 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0013427 increased memory-marker NK cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0013430 increased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0013433 increased KLRG1-positive CD4-positive, CD25-positive, alpha-beta regulatory T cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0013514 increased memory-marker CD4-negative NK T cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0013654 increased CD103-positive CD11b-low dendritic cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0013667 increased immature NK cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0013672 decreased mature NK cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0013675 decreased Ly6C-positive mature NK cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0013768 decreased marginal zone precursor B cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0013772 increased effector memory T-helper cell number IEA N RGD:5509061 20201231 MGI 736396 Arpc1b actin related protein 2/3 complex, subunit 1B gene MP:0013775 increased KLRG1-positive T-helper cell number IEA N RGD:5509061 20201231 MGI 736399 Hspa1b heat shock protein 1B gene MP:0003076 increased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:11739994 736399 Hspa1b heat shock protein 1B gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:12049720 736399 Hspa1b heat shock protein 1B gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17671199 736399 Hspa1b heat shock protein 1B gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12049720 736399 Hspa1b heat shock protein 1B gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:12049720 736399 Hspa1b heat shock protein 1B gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:17671199 736399 Hspa1b heat shock protein 1B gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11713291 736399 Hspa1b heat shock protein 1B gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:11739994 736399 Hspa1b heat shock protein 1B gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20150212 MGI PMID:12189176 736399 Hspa1b heat shock protein 1B gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:12049720 736399 Hspa1b heat shock protein 1B gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:11713291 736399 Hspa1b heat shock protein 1B gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12049720 736399 Hspa1b heat shock protein 1B gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17671199 736399 Hspa1b heat shock protein 1B gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12189176 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0000836 abnormal substantia nigra morphology IAGP N RGD:5509061 20141003 MGI PMID:9520484 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20016108 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17457314 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20016108 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:10506516 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20016108 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9092472 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15589522 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:20016108 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:9608532 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:10506516 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9092472 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:9092472 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0001905 abnormal dopamine level IAGP N RGD:5509061 20141003 MGI PMID:17457314 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:9092472 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:17457314 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:20016108 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:20016108 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:20016108 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20016108 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:9092472 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:9608532 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:15589522 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:20016108 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:20566846 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:9092472 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:10506516 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0003864 abnormal midbrain development IAGP N RGD:5509061 20141003 MGI PMID:9520484 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0003964 abnormal noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:17457314 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:17457314 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0004941 abnormal regulatory T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21468021 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21468021 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21468021 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0005322 abnormal serotonin level IAGP N RGD:5509061 20141003 MGI PMID:17457314 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:15589522 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:20016108 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:9092472 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:9520484 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:9608532 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0006100 abnormal tegmentum morphology IAGP N RGD:5509061 20141003 MGI PMID:9520484 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21468021 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:21468021 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21468021 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0008235 increased susceptibility to neuronal excitotoxicity IAGP N RGD:5509061 20141003 MGI PMID:20566846 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:21468021 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0009746 enhanced behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17457314 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0009749 enhanced behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:17457314 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0010069 increased serotonin level IAGP N RGD:5509061 20180927 MGI PMID:20016108 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:21468021 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21468021 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20016108 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10506516 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9092472 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9520484 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9608532 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21468021 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:20016108 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0012503 increased midbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9520484 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:10506516 736400 Nr4a2 nuclear receptor subfamily 4, group A, member 2 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:17457314 736403 Slc10a2 solute carrier family 10, member 2 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:12819193 736403 Slc10a2 solute carrier family 10, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12819193 736403 Slc10a2 solute carrier family 10, member 2 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12819193 736403 Slc10a2 solute carrier family 10, member 2 gene MP:0002647 decreased intestinal cholesterol absorption IAGP N RGD:5509061 20141003 MGI PMID:12819193 736403 Slc10a2 solute carrier family 10, member 2 gene MP:0002791 steatorrhea IAGP N RGD:5509061 20141003 MGI PMID:12819193 736403 Slc10a2 solute carrier family 10, member 2 gene MP:0004773 abnormal bile composition IAGP N RGD:5509061 20141003 MGI PMID:12819193 736403 Slc10a2 solute carrier family 10, member 2 gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:12819193 736403 Slc10a2 solute carrier family 10, member 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12819193 736403 Slc10a2 solute carrier family 10, member 2 gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:12819193 736403 Slc10a2 solute carrier family 10, member 2 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12819193 736403 Slc10a2 solute carrier family 10, member 2 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18292224 736403 Slc10a2 solute carrier family 10, member 2 gene MP:0010579 increased heart left ventricle size IEA N RGD:5509061 20210128 MGI 736403 Slc10a2 solute carrier family 10, member 2 gene MP:0014478 increased feces bile salt level IAGP N RGD:5509061 20240704 MGI PMID:12819193 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20210520 MGI 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20181227 MGI 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210520 MGI 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20181227 MGI 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21471385 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21471385 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:21471385 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0002546 mydriasis IEA N RGD:5509061 20201022 MGI 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20141003 MGI PMID:21471385 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20141003 MGI PMID:21471385 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0004958 enlarged prostate gland IEA N RGD:5509061 20210520 MGI 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:21471385 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:21471385 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:21471385 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0010052 increased grip strength IAGP N RGD:5509061 20141003 MGI PMID:21471385 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 736406 Dync1li1 dynein cytoplasmic 1 light intermediate chain 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20181227 MGI 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000111 cleft palate IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:12893741 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000288 abnormal pericardium morphology IEA N RGD:5509061 20181227 MGI 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000299 failure of atrioventricular cushion closure IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20141003 MGI 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000440 domed cranium IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000825 dilated lateral ventricle IAGP N RGD:5509061 20141003 MGI PMID:16481398 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000827 dilated third ventricle IAGP N RGD:5509061 20141003 MGI PMID:16481398 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000828 abnormal fourth ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16481398 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:16481398 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:16481398 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000914 exencephaly IEA N RGD:5509061 20141003 MGI 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16481398 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12893741 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20861308 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001785 edema IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:16481398 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20141003 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0001914 hemorrhage IEA N RGD:5509061 20210520 MGI 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0002639 micrognathia IEA N RGD:5509061 20141003 MGI 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20231214 MGI PMID:20861308 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0003052 omphalocele IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:20861308 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0004062 dilated heart right atrium IAGP N RGD:5509061 20141003 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:20861308 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0004258 abnormal placenta size IEA N RGD:5509061 20170504 MGI 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0004320 split sternum IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0005170 cleft upper lip IEA N RGD:5509061 20141003 MGI 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0005244 hemopericardium IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:12893741 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:20861308 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0005537 abnormal cerebral aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:20861308 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:16481398 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0006009 abnormal neuronal migration IAGP N RGD:5509061 20141003 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0006096 absent retina bipolar cells IAGP N RGD:5509061 20231214 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:16481398 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20231214 MGI PMID:12893741 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20231214 MGI PMID:20861308 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20231214 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0009688 abnormal spinal cord central canal morphology IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0009698 heart hemorrhage IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0009701 abnormal birth body size IAGP N RGD:5509061 20231214 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0009760 abnormal mitotic spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:20861308 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20231214 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010146 umbilical hernia IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010449 heart right ventricle outflow tract stenosis IAGP N RGD:5509061 20141003 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010561 absent coronary vessels IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0010912 herniated liver IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19815823 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16481398 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20861308 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20170504 MGI 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20231214 MGI PMID:12893741 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011660 ectopia cordis IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0012515 abnormal heart apex morphology IAGP N RGD:5509061 20180201 MGI PMID:29084269 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20141003 MGI PMID:16481398 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0013283 failure of ventral body wall closure IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0013807 generalized edema IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0014327 decreased Purkinje cell size IAGP N RGD:5509061 20240118 MGI PMID:15034141 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0020850 abnormal microtubule cytoskeleton morphology IAGP N RGD:5509061 20231214 MGI PMID:20861308 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20231214 MGI PMID:20861308 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0031462 decreased palatal shelf size IAGP N RGD:5509061 20230420 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0031550 abnormal atrioventricular valve development IAGP N RGD:5509061 20240104 MGI PMID:24825879 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0031609 increased fetal cardiomyocyte size IAGP N RGD:5509061 20240321 MGI PMID:12893741 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0031609 increased fetal cardiomyocyte size IAGP N RGD:5509061 20240321 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0031609 increased fetal cardiomyocyte size IAGP N RGD:5509061 20240321 MGI PMID:9356462 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0031611 decreased fetal cardiomyocyte number IAGP N RGD:5509061 20240321 MGI PMID:12893741 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0031611 decreased fetal cardiomyocyte number IAGP N RGD:5509061 20240321 MGI PMID:17519229 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0031611 decreased fetal cardiomyocyte number IAGP N RGD:5509061 20240321 MGI PMID:20861308 736408 Myh10 myosin, heavy polypeptide 10, non-muscle gene MP:0031613 fetal cardiomyocyte disarray IAGP N RGD:5509061 20240321 MGI PMID:9356462 736417 Rrad Ras-related associated with diabetes gene MP:0002626 increased heart rate IEA N RGD:5509061 20170105 MGI 736417 Rrad Ras-related associated with diabetes gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:18056528 736417 Rrad Ras-related associated with diabetes gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 736417 Rrad Ras-related associated with diabetes gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18056528 736417 Rrad Ras-related associated with diabetes gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20210520 MGI 736417 Rrad Ras-related associated with diabetes gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 736417 Rrad Ras-related associated with diabetes gene MP:0010507 shortened RR interval IEA N RGD:5509061 20170105 MGI 736417 Rrad Ras-related associated with diabetes gene MP:0010571 shortened ST segment IEA N RGD:5509061 20170105 MGI 736420 Gjb5 gap junction protein, beta 5 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:17961533 736420 Gjb5 gap junction protein, beta 5 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17961533 736420 Gjb5 gap junction protein, beta 5 gene MP:0004921 decreased placenta weight IAGP N RGD:5509061 20141003 MGI PMID:17961533 736420 Gjb5 gap junction protein, beta 5 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:17961533 736420 Gjb5 gap junction protein, beta 5 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17961533 736422 Ctsj cathepsin J gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 736423 Fxyd2 FXYD domain-containing ion transport regulator 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15755730 736426 Hivep1 human immunodeficiency virus type I enhancer binding protein 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210128 MGI 736426 Hivep1 human immunodeficiency virus type I enhancer binding protein 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210128 MGI 736426 Hivep1 human immunodeficiency virus type I enhancer binding protein 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20240523 MGI 736426 Hivep1 human immunodeficiency virus type I enhancer binding protein 1 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 736426 Hivep1 human immunodeficiency virus type I enhancer binding protein 1 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 736426 Hivep1 human immunodeficiency virus type I enhancer binding protein 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20231207 MGI 736426 Hivep1 human immunodeficiency virus type I enhancer binding protein 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 736426 Hivep1 human immunodeficiency virus type I enhancer binding protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0000026 abnormal inner ear morphology IAGP N RGD:5509061 20150319 MGI PMID:24760582 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20150319 MGI PMID:24760582 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0000034 abnormal inner ear vestibule morphology IAGP N RGD:5509061 20141003 MGI PMID:20442411 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0000042 abnormal organ of Corti morphology IEA N RGD:5509061 20111116 MGI 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:14690057 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:15320950 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0000045 abnormal hair cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20210128 MGI PMID:31155292 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0000681 abnormal thyroid gland morphology IAGP N RGD:5509061 20150319 MGI PMID:24760582 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210128 MGI PMID:31155292 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:17200157 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:20442411 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001394 circling IAGP N RGD:5509061 20210128 MGI PMID:31155292 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001395 bidirectional circling IEA N RGD:5509061 20161201 MGI 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20442411 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001410 head bobbing IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001525 impaired balance IAGP N RGD:5509061 20210128 MGI PMID:31155292 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001526 abnormal placing response IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:17299139 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:20442411 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0002428 abnormal semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:20442411 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0002675 asthenozoospermia IEA N RGD:5509061 20111116 MGI 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0002687 oligozoospermia IEA N RGD:5509061 20111116 MGI 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0002894 abnormal otolith morphology IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0002895 abnormal otolithic membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0002895 abnormal otolithic membrane morphology IAGP N RGD:5509061 20151001 MGI PMID:20442411 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0002978 absent otoliths IAGP N RGD:5509061 20141003 MGI PMID:20442411 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0003016 increased circulating bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:20375274 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0003143 enlarged otoliths IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0003143 enlarged otoliths IAGP N RGD:5509061 20141003 MGI PMID:15320950 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0003143 enlarged otoliths IAGP N RGD:5509061 20141003 MGI PMID:17200157 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0003143 enlarged otoliths IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0003143 enlarged otoliths IAGP N RGD:5509061 20210128 MGI PMID:31155292 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0003144 decreased otolith number IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0003145 detached otolithic membrane IAGP N RGD:5509061 20210128 MGI PMID:31155292 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0003146 absent cochlear ganglion IEA N RGD:5509061 20111116 MGI 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0003148 decreased cochlea coiling IEA N RGD:5509061 20111116 MGI 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20150319 MGI PMID:24760582 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0003169 abnormal scala media morphology IEA N RGD:5509061 20111116 MGI 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0003205 testicular atrophy IEA N RGD:5509061 20111116 MGI 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20150319 MGI PMID:24760582 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17200157 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17299139 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004249 abnormal crista ampullaris morphology IAGP N RGD:5509061 20141003 MGI PMID:20442411 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004287 abnormal spiral limbus morphology IAGP N RGD:5509061 20141003 MGI PMID:15320950 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004316 enlarged vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004324 vestibular hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004328 decreased vestibular hair cell number IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004331 vestibular saccular macula degeneration IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004334 utricular macular degeneration IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15320950 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:23755160 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20150319 MGI PMID:24760582 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20210128 MGI PMID:31155292 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20141003 MGI PMID:14690057 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20141003 MGI PMID:15320950 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004363 stria vascularis degeneration IAGP N RGD:5509061 20141003 MGI PMID:23755160 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004364 thin stria vascularis IAGP N RGD:5509061 20141003 MGI PMID:14690057 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004365 abnormal strial basal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14690057 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004365 abnormal strial basal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15320950 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004366 abnormal strial marginal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14690057 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004366 abnormal strial marginal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15320950 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004366 abnormal strial marginal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004367 abnormal strial intermediate cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14690057 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004367 abnormal strial intermediate cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15320950 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20150319 MGI PMID:24760582 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20150319 MGI PMID:24760582 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004405 absent cochlear hair cells IEA N RGD:5509061 20111116 MGI 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004408 decreased cochlear hair cell number IEA N RGD:5509061 20111116 MGI 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004410 absent endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:14690057 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004410 absent endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:15320950 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:17299139 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004487 type I spiral ligament fibrocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:15320950 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004488 type II spiral ligament fibrocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:15320950 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004493 dilated cochlea IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004493 dilated cochlea IAGP N RGD:5509061 20141003 MGI PMID:14690057 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20150319 MGI PMID:24760582 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology IAGP N RGD:5509061 20210128 MGI PMID:31155292 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004533 fused inner hair cell stereocilia IAGP N RGD:5509061 20210128 MGI PMID:31155292 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004591 enlarged tectorial membrane IAGP N RGD:5509061 20150319 MGI PMID:24760582 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20150319 MGI PMID:24760582 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:14690057 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:20442411 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004749 nonsyndromic hearing loss IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004862 small scala tympani IAGP N RGD:5509061 20141003 MGI PMID:14690057 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004863 thin spiral ligament IAGP N RGD:5509061 20141003 MGI PMID:14690057 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004863 thin spiral ligament IAGP N RGD:5509061 20141003 MGI PMID:15320950 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:17200157 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0005191 head tilt IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0005307 head tossing IEA N RGD:5509061 20161201 MGI 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006011 abnormal endolymphatic duct morphology IAGP N RGD:5509061 20141003 MGI PMID:23755160 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:14690057 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006012 dilated endolymphatic duct IAGP N RGD:5509061 20150319 MGI PMID:24760582 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006014 dilated endolymphatic sac IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006014 dilated endolymphatic sac IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006025 distended Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006025 distended Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:15320950 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006089 abnormal vestibular saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:20442411 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006090 abnormal utricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20442411 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20210128 MGI PMID:31155292 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:20442411 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006389 abnormal vestibular endolymph physiology IAGP N RGD:5509061 20141003 MGI PMID:17200157 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006391 abnormal vestibular endolymph ionic homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17200157 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0006403 abnormal cochlear endolymph ionic homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17299139 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0008309 dilated scala media IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0008309 dilated scala media IAGP N RGD:5509061 20141003 MGI PMID:15320950 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0008309 dilated scala media IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0008309 dilated scala media IAGP N RGD:5509061 20141003 MGI PMID:23755160 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0008537 increased susceptibility to induced colitis IEA N RGD:5509061 20161201 MGI 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0009350 decreased urine pH IAGP N RGD:5509061 20141003 MGI PMID:20375274 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0009821 abnormal vestibular aqueduct morphology IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0011735 increased urine ammonia level IAGP N RGD:5509061 20141003 MGI PMID:20375274 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11152663 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:17299139 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:20442411 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:21811566 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20210128 MGI PMID:31155292 736429 Slc26a4 solute carrier family 26, member 4 gene MP:0030126 torticollis IAGP N RGD:5509061 20210128 MGI PMID:31155292 736430 Arg1 arginase, liver gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12052859 736430 Arg1 arginase, liver gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:12052859 736430 Arg1 arginase, liver gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:12052859 736430 Arg1 arginase, liver gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12052859 736430 Arg1 arginase, liver gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:12052859 736430 Arg1 arginase, liver gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18978793 736430 Arg1 arginase, liver gene MP:0002138 abnormal hepatobiliary system morphology IAGP N RGD:5509061 20141003 MGI PMID:12052859 736430 Arg1 arginase, liver gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17450126 736430 Arg1 arginase, liver gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18978793 736430 Arg1 arginase, liver gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18978793 736430 Arg1 arginase, liver gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:22416259 736430 Arg1 arginase, liver gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:17450126 736430 Arg1 arginase, liver gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18978793 736430 Arg1 arginase, liver gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:18978793 736430 Arg1 arginase, liver gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:12052859 736430 Arg1 arginase, liver gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:12052859 736430 Arg1 arginase, liver gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22416259 736430 Arg1 arginase, liver gene MP:0011076 increased macrophage nitric oxide production IAGP N RGD:5509061 20141003 MGI PMID:18978793 736430 Arg1 arginase, liver gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12052859 736430 Arg1 arginase, liver gene MP:0011652 increased circulating histidine level IAGP N RGD:5509061 20180712 MGI PMID:12052859 736430 Arg1 arginase, liver gene MP:0020836 increased circulating citrulline level IAGP N RGD:5509061 20180712 MGI PMID:12052859 736430 Arg1 arginase, liver gene MP:0030651 decreased circulating ornithine level IAGP N RGD:5509061 20180913 MGI PMID:12052859 736430 Arg1 arginase, liver gene MP:0030661 increased circulating arginine level IAGP N RGD:5509061 20180913 MGI PMID:12052859 736430 Arg1 arginase, liver gene MP:0030668 decreased circulating proline level IAGP N RGD:5509061 20180913 MGI PMID:12052859 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19686689 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:19686689 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8951051 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8951051 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19686689 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:8951051 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:8951051 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:8951051 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:19686689 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:8951051 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19686689 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0004197 abnormal fetal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:8951051 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0010885 absent trachea IAGP N RGD:5509061 20141003 MGI PMID:19686689 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19686689 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8951051 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0011142 abnormal lung-associated mesenchyme development IAGP N RGD:5509061 20141003 MGI PMID:19686689 736432 Wnt2 wingless-type MMTV integration site family, member 2 gene MP:0011148 decreased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20141003 MGI PMID:19686689 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0000264 failure of vascular branching IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0000298 absent atrioventricular cushions IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:1347918 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8577718 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:8944029 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16792508 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0003974 abnormal endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:8577718 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0006056 increased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0008172 abnormal follicular B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0008181 increased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0008188 abnormal transitional stage B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0008206 increased B-2 B cell number IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18249142 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0009328 delayed heart looping IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:12588999 736434 Ptprj protein tyrosine phosphatase receptor type J gene MP:0014469 abnormal B cell calcium ion homeostasis IAGP N RGD:5509061 20240613 MGI PMID:18249142 736438 Map1a microtubule-associated protein 1 A gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20160616 MGI PMID:25788676 736438 Map1a microtubule-associated protein 1 A gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20160616 MGI PMID:25788676 736438 Map1a microtubule-associated protein 1 A gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20160616 MGI PMID:25788676 736438 Map1a microtubule-associated protein 1 A gene MP:0001393 ataxia IAGP N RGD:5509061 20160616 MGI PMID:25788676 736438 Map1a microtubule-associated protein 1 A gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20160616 MGI PMID:25788676 736438 Map1a microtubule-associated protein 1 A gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20160616 MGI PMID:25788676 736438 Map1a microtubule-associated protein 1 A gene MP:0010733 abnormal axon initial segment morphology IAGP N RGD:5509061 20160616 MGI PMID:25788676 736438 Map1a microtubule-associated protein 1 A gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20180913 MGI PMID:10441341 736438 Map1a microtubule-associated protein 1 A gene MP:0020850 abnormal microtubule cytoskeleton morphology IAGP N RGD:5509061 20190718 MGI PMID:25788676 736441 Foxd3 forkhead box D3 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12381664 736441 Foxd3 forkhead box D3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20171019 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0001044 abnormal enteric nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:12381664 736441 Foxd3 forkhead box D3 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:12381664 736441 Foxd3 forkhead box D3 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:12381664 736441 Foxd3 forkhead box D3 gene MP:0001705 abnormal proximal-distal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12381664 736441 Foxd3 forkhead box D3 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:16039639 736441 Foxd3 forkhead box D3 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:12381664 736441 Foxd3 forkhead box D3 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12381664 736441 Foxd3 forkhead box D3 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:12381664 736441 Foxd3 forkhead box D3 gene MP:0003994 abnormal dorsal spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0004376 absent frontal bone IAGP N RGD:5509061 20171019 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0004384 small interparietal bone IAGP N RGD:5509061 20171019 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0004418 small parietal bone IAGP N RGD:5509061 20171019 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0004447 small basioccipital bone IAGP N RGD:5509061 20171019 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16039639 736441 Foxd3 forkhead box D3 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0006346 small pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0008384 absent nasal capsule IAGP N RGD:5509061 20171019 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12381664 736441 Foxd3 forkhead box D3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12381664 736441 Foxd3 forkhead box D3 gene MP:0011189 small embryonic epiblast IAGP N RGD:5509061 20141003 MGI PMID:12381664 736441 Foxd3 forkhead box D3 gene MP:0011192 decreased embryonic epiblast cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12381664 736441 Foxd3 forkhead box D3 gene MP:0011255 abnormal anterior visceral endoderm cell migration IAGP N RGD:5509061 20141003 MGI PMID:12381664 736441 Foxd3 forkhead box D3 gene MP:0012100 absent spongiotrophoblast IAGP N RGD:5509061 20141003 MGI PMID:16039639 736441 Foxd3 forkhead box D3 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0012729 abnormal common carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0012752 abnormal cardiac neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0013006 abnormal enteric neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:18367558 736441 Foxd3 forkhead box D3 gene MP:0030223 mandibular hyperostosis IAGP N RGD:5509061 20171019 MGI PMID:18367558 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000153 rib bifurcation IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000154 rib fusion IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:12941803 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:16195383 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:14633735 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:12782272 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12782272 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000443 abnormal snout morphology IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000445 short snout IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000597 delayed hepatic development IAGP N RGD:5509061 20141003 MGI PMID:12782272 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:17044021 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000636 enlarged pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000642 enlarged adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12782272 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:17044021 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17893233 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19208834 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20230302 MGI PMID:35194044 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12782272 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20230302 MGI PMID:35194044 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001729 impaired embryo implantation IAGP N RGD:5509061 20230302 MGI PMID:35194044 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12782272 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20230302 MGI PMID:35194044 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20230302 MGI PMID:35194044 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:17044021 736444 Men1 multiple endocrine neoplasia 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002031 increased adrenal gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17044021 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002050 increased pheochromocytoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12917331 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12941803 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19208834 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17893233 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19208834 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21788502 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12782272 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:19208834 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:21788502 736444 Men1 multiple endocrine neoplasia 1 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003112 enlarged parathyroid gland IAGP N RGD:5509061 20150305 MGI PMID:14633735 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003364 increased insulinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003364 increased insulinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12917331 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003364 increased insulinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12941803 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003364 increased insulinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15060136 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003364 increased insulinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17044021 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003364 increased insulinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19208834 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003364 increased insulinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21788502 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003365 increased glucagonoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003365 increased glucagonoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17044021 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003430 increased pancreatic islet cell adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003430 increased pancreatic islet cell adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003430 increased pancreatic islet cell adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003493 parathyroid gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17044021 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003493 parathyroid gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003495 increased parathyroid adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003495 increased parathyroid adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003495 increased parathyroid adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17044021 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003495 increased parathyroid adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003495 increased parathyroid adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003496 increased thyroid adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003498 thyroid gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003498 thyroid gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17044021 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003505 increased prolactinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003505 increased prolactinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003505 increased prolactinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15060136 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003505 increased prolactinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17044021 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:16195383 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:12782272 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003845 abnormal decidualization IAGP N RGD:5509061 20230302 MGI PMID:35194044 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20230302 MGI PMID:35194044 736444 Men1 multiple endocrine neoplasia 1 gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0004832 enlarged ovary IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20230302 MGI PMID:35194044 736444 Men1 multiple endocrine neoplasia 1 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:12782272 736444 Men1 multiple endocrine neoplasia 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:19208834 736444 Men1 multiple endocrine neoplasia 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:21788502 736444 Men1 multiple endocrine neoplasia 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12917331 736444 Men1 multiple endocrine neoplasia 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12941803 736444 Men1 multiple endocrine neoplasia 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15060136 736444 Men1 multiple endocrine neoplasia 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17044021 736444 Men1 multiple endocrine neoplasia 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19208834 736444 Men1 multiple endocrine neoplasia 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21788502 736444 Men1 multiple endocrine neoplasia 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12917331 736444 Men1 multiple endocrine neoplasia 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19208834 736444 Men1 multiple endocrine neoplasia 1 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 736444 Men1 multiple endocrine neoplasia 1 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17044021 736444 Men1 multiple endocrine neoplasia 1 gene MP:0008000 increased ovary tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 736444 Men1 multiple endocrine neoplasia 1 gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 736444 Men1 multiple endocrine neoplasia 1 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0008876 decreased uterine NK cell number IAGP N RGD:5509061 20230302 MGI PMID:35194044 736444 Men1 multiple endocrine neoplasia 1 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20230302 MGI PMID:35194044 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009043 increased pancreas adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17044021 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009044 increased adrenal gland adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009044 increased adrenal gland adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17044021 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009148 pancreas necrosis IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15060136 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009153 increased pancreas tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:19208834 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009247 meteorism IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009308 increased adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009590 increased gonad tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009592 increased Leydig cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009592 increased Leydig cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17044021 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009592 increased Leydig cell tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14633735 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010288 increased gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010288 increased gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:17409423 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010316 increased thyroid tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010320 increased pituitary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010321 increased parathyroid gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17409423 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010321 increased parathyroid gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010321 increased parathyroid gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010345 increased thyroid C-cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010348 increased pancreatic islet cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010350 increased pituitary adenohypophysis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010350 increased pituitary adenohypophysis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010350 increased pituitary adenohypophysis tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010351 increased pituitary melanotroph tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17893233 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010366 increased adrenal cortical tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010366 increased adrenal cortical tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010390 increased adrenocortical adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12819299 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:12782272 736444 Men1 multiple endocrine neoplasia 1 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17409423 736444 Men1 multiple endocrine neoplasia 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14992727 736444 Men1 multiple endocrine neoplasia 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12782272 736444 Men1 multiple endocrine neoplasia 1 gene MP:0013401 increased endometrial gland number IAGP N RGD:5509061 20230302 MGI PMID:35194044 736444 Men1 multiple endocrine neoplasia 1 gene MP:0013528 thyroid gland cyst IAGP N RGD:5509061 20150219 MGI PMID:11158604 736444 Men1 multiple endocrine neoplasia 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:19620250 736444 Men1 multiple endocrine neoplasia 1 gene MP:0021210 bilateral cleft palate IAGP N RGD:5509061 20221201 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230302 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0021216 abnormal palatal mesenchymal cell differentiation IAGP N RGD:5509061 20230302 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0021217 abnormal palatal shelf bone ossification IAGP N RGD:5509061 20230223 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0030291 short soft palate IAGP N RGD:5509061 20221020 MGI PMID:17927973 736444 Men1 multiple endocrine neoplasia 1 gene MP:0031434 increased miscarriage rate IAGP N RGD:5509061 20230302 MGI PMID:35194044 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0000217 abnormal leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11420040 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11420040 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:21724994 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0000745 tremors IEA N RGD:5509061 20181227 MGI 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20210128 MGI 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:11911824 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0001798 impaired macrophage phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:8769481 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:21724994 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18949059 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:18949059 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:11911824 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:11420040 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0002531 abnormal type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11911824 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0002626 increased heart rate IEA N RGD:5509061 20230601 MGI 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0003233 prolonged QT interval IEA N RGD:5509061 20240523 MGI 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:12528127 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21724994 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:21724994 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:21724994 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12576552 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0004828 decreased susceptibility to autoimmune hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:11911824 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0004829 increased anti-chromatin antibody level IAGP N RGD:5509061 20141003 MGI PMID:21724994 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:21724994 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:21724994 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:8769481 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:18949059 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10330436 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0005612 decreased susceptibility to type II hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:8769481 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:11420040 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0008765 decreased mast cell degranulation IAGP N RGD:5509061 20141003 MGI PMID:8769481 736451 Fcgr3 Fc receptor, IgG, low affinity III gene MP:0010091 decreased circulating creatine kinase level IEA N RGD:5509061 20210128 MGI 736454 Nlgn1 neuroligin 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16982420 736454 Nlgn1 neuroligin 1 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20200402 MGI PMID:28841651 736454 Nlgn1 neuroligin 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:16982420 736454 Nlgn1 neuroligin 1 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:16982420 736454 Nlgn1 neuroligin 1 gene MP:0002068 abnormal parental behavior IAGP N RGD:5509061 20141003 MGI PMID:16982420 736454 Nlgn1 neuroligin 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 736454 Nlgn1 neuroligin 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:16982420 736454 Nlgn1 neuroligin 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20160414 MGI PMID:26291161 736454 Nlgn1 neuroligin 1 gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20160414 MGI PMID:26291161 736454 Nlgn1 neuroligin 1 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:16982420 736454 Nlgn1 neuroligin 1 gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20200402 MGI PMID:28841651 736454 Nlgn1 neuroligin 1 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20200402 MGI PMID:28841651 736454 Nlgn1 neuroligin 1 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20160414 MGI PMID:26291161 736454 Nlgn1 neuroligin 1 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20160414 MGI PMID:26291161 736454 Nlgn1 neuroligin 1 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20160414 MGI PMID:26291161 736454 Nlgn1 neuroligin 1 gene MP:0010746 abnormal pre-Botzinger complex physiology IAGP N RGD:5509061 20141003 MGI PMID:16982420 736454 Nlgn1 neuroligin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16982420 736454 Nlgn1 neuroligin 1 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20160414 MGI PMID:26291161 736454 Nlgn1 neuroligin 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20200402 MGI PMID:28841651 736454 Nlgn1 neuroligin 1 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:26291161 736454 Nlgn1 neuroligin 1 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:26291161 736457 Myl3 myosin, light polypeptide 3 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20240215 MGI PMID:37794006 736457 Myl3 myosin, light polypeptide 3 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20240215 MGI PMID:37794006 736457 Myl3 myosin, light polypeptide 3 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20181227 MGI 736457 Myl3 myosin, light polypeptide 3 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20240215 MGI PMID:37794006 736457 Myl3 myosin, light polypeptide 3 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20181227 MGI 736461 Alox5ap arachidonate 5-lipoxygenase activating protein gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9091585 736461 Alox5ap arachidonate 5-lipoxygenase activating protein gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:9091585 736461 Alox5ap arachidonate 5-lipoxygenase activating protein gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:9091580 736461 Alox5ap arachidonate 5-lipoxygenase activating protein gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:9091580 736461 Alox5ap arachidonate 5-lipoxygenase activating protein gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:9091580 736461 Alox5ap arachidonate 5-lipoxygenase activating protein gene MP:0009811 abnormal prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:9091585 736461 Alox5ap arachidonate 5-lipoxygenase activating protein gene MP:0009813 abnormal leukotriene level IAGP N RGD:5509061 20141003 MGI PMID:9091585 736461 Alox5ap arachidonate 5-lipoxygenase activating protein gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:9091580 736461 Alox5ap arachidonate 5-lipoxygenase activating protein gene MP:0009817 decreased leukotriene level IAGP N RGD:5509061 20141003 MGI PMID:9091580 736461 Alox5ap arachidonate 5-lipoxygenase activating protein gene MP:0009817 decreased leukotriene level IAGP N RGD:5509061 20141003 MGI PMID:9091585 736461 Alox5ap arachidonate 5-lipoxygenase activating protein gene MP:0009818 abnormal thromboxane level IAGP N RGD:5509061 20141003 MGI PMID:9091580 736463 Rab28 RAB28, member RAS oncogene family gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220811 MGI 736463 Rab28 RAB28, member RAS oncogene family gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20191003 MGI PMID:30228185 736463 Rab28 RAB28, member RAS oncogene family gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 736463 Rab28 RAB28, member RAS oncogene family gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20220811 MGI 736463 Rab28 RAB28, member RAS oncogene family gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 736463 Rab28 RAB28, member RAS oncogene family gene MP:0002834 decreased heart weight IEA N RGD:5509061 20201022 MGI 736463 Rab28 RAB28, member RAS oncogene family gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 736463 Rab28 RAB28, member RAS oncogene family gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20220811 MGI 736463 Rab28 RAB28, member RAS oncogene family gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20191003 MGI PMID:30228185 736463 Rab28 RAB28, member RAS oncogene family gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 736463 Rab28 RAB28, member RAS oncogene family gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20191003 MGI PMID:30228185 736463 Rab28 RAB28, member RAS oncogene family gene MP:0008449 abnormal retina cone cell outer segment morphology IAGP N RGD:5509061 20191003 MGI PMID:30228185 736463 Rab28 RAB28, member RAS oncogene family gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20191003 MGI PMID:30228185 736463 Rab28 RAB28, member RAS oncogene family gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20220811 MGI 736463 Rab28 RAB28, member RAS oncogene family gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 736463 Rab28 RAB28, member RAS oncogene family gene MP:0011997 abnormal retina outer nuclear layer thickness IAGP N RGD:5509061 20191003 MGI PMID:30228185 736463 Rab28 RAB28, member RAS oncogene family gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20191003 MGI PMID:30228185 736463 Rab28 RAB28, member RAS oncogene family gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20191003 MGI PMID:30228185 736463 Rab28 RAB28, member RAS oncogene family gene MP:0014332 long retina cone cell outer segment IAGP N RGD:5509061 20240118 MGI PMID:30228185 736463 Rab28 RAB28, member RAS oncogene family gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:30228185 736465 Ssbp1 single-stranded DNA binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736471 Ctf1 cardiotrophin 1 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:11160399 736471 Ctf1 cardiotrophin 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0008034 enhanced lipolysis IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0009167 increased pancreatic islet number IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0009171 enlarged pancreatic islets IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:11160399 736471 Ctf1 cardiotrophin 1 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:21803294 736471 Ctf1 cardiotrophin 1 gene MP:0014396 decreased fat cell mitochondrial DNA content IAGP N RGD:5509061 20240321 MGI PMID:21803294 736476 Ralgds ral guanine nucleotide dissociation stimulator gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:15766660 736476 Ralgds ral guanine nucleotide dissociation stimulator gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:15766660 736482 Calb1 calbindin 1 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0000160 kyphosis IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0000692 small spleen IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16860487 736482 Calb1 calbindin 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 736482 Calb1 calbindin 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9037080 736482 Calb1 calbindin 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:12716955 736482 Calb1 calbindin 1 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:12716955 736482 Calb1 calbindin 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 736482 Calb1 calbindin 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:9037080 736482 Calb1 calbindin 1 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:12716955 736482 Calb1 calbindin 1 gene MP:0004844 abnormal vestibuloocular reflex IAGP N RGD:5509061 20141003 MGI PMID:12716955 736482 Calb1 calbindin 1 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20230601 MGI 736482 Calb1 calbindin 1 gene MP:0014331 abnormal Purkinje cell mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:16860487 736485 Sqstm1 sequestosome 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21515589 736485 Sqstm1 sequestosome 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20200213 MGI PMID:29555685 736485 Sqstm1 sequestosome 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20240118 MGI PMID:37306101 736485 Sqstm1 sequestosome 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20240118 MGI PMID:37306101 736485 Sqstm1 sequestosome 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18083104 736485 Sqstm1 sequestosome 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:18083104 736485 Sqstm1 sequestosome 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:18083104 736485 Sqstm1 sequestosome 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20240118 MGI PMID:37306101 736485 Sqstm1 sequestosome 1 gene MP:0001257 increased body length IEA N RGD:5509061 20160804 MGI 736485 Sqstm1 sequestosome 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:24027277 736485 Sqstm1 sequestosome 1 gene MP:0001261 obese IAGP N RGD:5509061 20200213 MGI PMID:29555685 736485 Sqstm1 sequestosome 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:18083104 736485 Sqstm1 sequestosome 1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:18765443 736485 Sqstm1 sequestosome 1 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20200213 MGI PMID:29555685 736485 Sqstm1 sequestosome 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:18083104 736485 Sqstm1 sequestosome 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20240118 MGI PMID:37306101 736485 Sqstm1 sequestosome 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22222206 736485 Sqstm1 sequestosome 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:21515589 736485 Sqstm1 sequestosome 1 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18083104 736485 Sqstm1 sequestosome 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:18083104 736485 Sqstm1 sequestosome 1 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20200213 MGI PMID:29555685 736485 Sqstm1 sequestosome 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18083104 736485 Sqstm1 sequestosome 1 gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:18083104 736485 Sqstm1 sequestosome 1 gene MP:0003325 decreased liver function IAGP N RGD:5509061 20141003 MGI PMID:18083104 736485 Sqstm1 sequestosome 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18083104 736485 Sqstm1 sequestosome 1 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:22222206 736485 Sqstm1 sequestosome 1 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:22222206 736485 Sqstm1 sequestosome 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:21515589 736485 Sqstm1 sequestosome 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20200213 MGI PMID:29555685 736485 Sqstm1 sequestosome 1 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21515589 736485 Sqstm1 sequestosome 1 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0004546 esophagus hyperplasia IAGP N RGD:5509061 20240118 MGI PMID:37306101 736485 Sqstm1 sequestosome 1 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20160804 MGI 736485 Sqstm1 sequestosome 1 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:21515589 736485 Sqstm1 sequestosome 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:21515589 736485 Sqstm1 sequestosome 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:14960283 736485 Sqstm1 sequestosome 1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20200213 MGI PMID:29555685 736485 Sqstm1 sequestosome 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20240118 MGI PMID:37306101 736485 Sqstm1 sequestosome 1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:22222206 736485 Sqstm1 sequestosome 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:24027277 736485 Sqstm1 sequestosome 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:18083104 736485 Sqstm1 sequestosome 1 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20240118 MGI PMID:37306101 736485 Sqstm1 sequestosome 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:18083104 736485 Sqstm1 sequestosome 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20240118 MGI PMID:37306101 736485 Sqstm1 sequestosome 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20160804 MGI 736485 Sqstm1 sequestosome 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 736485 Sqstm1 sequestosome 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20240118 MGI PMID:37306101 736485 Sqstm1 sequestosome 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:24027277 736485 Sqstm1 sequestosome 1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:22222206 736485 Sqstm1 sequestosome 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21515589 736485 Sqstm1 sequestosome 1 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:14960283 736485 Sqstm1 sequestosome 1 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:18765443 736485 Sqstm1 sequestosome 1 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21515589 736485 Sqstm1 sequestosome 1 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20200213 MGI PMID:29555685 736485 Sqstm1 sequestosome 1 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:14960283 736485 Sqstm1 sequestosome 1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22222206 736485 Sqstm1 sequestosome 1 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:24027277 736485 Sqstm1 sequestosome 1 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0009972 absent hippocampus pyramidal cells IAGP N RGD:5509061 20141003 MGI PMID:18083104 736485 Sqstm1 sequestosome 1 gene MP:0009975 absent cerebral cortex pyramidal cells IAGP N RGD:5509061 20141003 MGI PMID:18083104 736485 Sqstm1 sequestosome 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0010179 rough coat IAGP N RGD:5509061 20141003 MGI PMID:22222206 736485 Sqstm1 sequestosome 1 gene MP:0010784 abnormal forestomach morphology IAGP N RGD:5509061 20240118 MGI PMID:37306101 736485 Sqstm1 sequestosome 1 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20200213 MGI PMID:29555685 736485 Sqstm1 sequestosome 1 gene MP:0010875 increased bone volume IAGP N RGD:5509061 20200213 MGI PMID:29555685 736485 Sqstm1 sequestosome 1 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:22222206 736485 Sqstm1 sequestosome 1 gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0011014 decreased core body temperature IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0011635 abnormal mitochondrial crista morphology IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0011636 disorganized mitochondrial cristae IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0011699 abnormal brown adipose tissue thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:23257354 736485 Sqstm1 sequestosome 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:24027277 736485 Sqstm1 sequestosome 1 gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20200213 MGI PMID:29555685 736485 Sqstm1 sequestosome 1 gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20200213 MGI PMID:29555685 736485 Sqstm1 sequestosome 1 gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20170202 MGI PMID:24027277 736485 Sqstm1 sequestosome 1 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:22222206 736487 Slco2b1 solute carrier organic anion transporter family, member 2b1 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 736487 Slco2b1 solute carrier organic anion transporter family, member 2b1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20210506 MGI PMID:32114507 736487 Slco2b1 solute carrier organic anion transporter family, member 2b1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20210506 MGI PMID:32114507 736489 Ccne1 cyclin E1 gene MP:0000228 abnormal thrombopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16023597 736489 Ccne1 cyclin E1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:18559482 736489 Ccne1 cyclin E1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:18559482 736489 Ccne1 cyclin E1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16023597 736489 Ccne1 cyclin E1 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18559482 736489 Ccne1 cyclin E1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:18559482 736489 Ccne1 cyclin E1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18559482 736489 Ccne1 cyclin E1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:21944720 736489 Ccne1 cyclin E1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21944720 736489 Ccne1 cyclin E1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:18559482 736489 Ccne1 cyclin E1 gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:12970191 736489 Ccne1 cyclin E1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0001902 reduced NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21944720 736489 Ccne1 cyclin E1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0001940 testis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16023597 736489 Ccne1 cyclin E1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12970191 736489 Ccne1 cyclin E1 gene MP:0002088 abnormal embryonic growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:12970191 736489 Ccne1 cyclin E1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21944720 736489 Ccne1 cyclin E1 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:18559482 736489 Ccne1 cyclin E1 gene MP:0002397 abnormal bone marrow morphology IAGP N RGD:5509061 20141003 MGI PMID:18559482 736489 Ccne1 cyclin E1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18559482 736489 Ccne1 cyclin E1 gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:18559482 736489 Ccne1 cyclin E1 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:21944720 736489 Ccne1 cyclin E1 gene MP:0003135 increased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:18559482 736489 Ccne1 cyclin E1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12970191 736489 Ccne1 cyclin E1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12970191 736489 Ccne1 cyclin E1 gene MP:0004028 chromosome breakage IAGP N RGD:5509061 20141003 MGI PMID:16023597 736489 Ccne1 cyclin E1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16023597 736489 Ccne1 cyclin E1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12970191 736489 Ccne1 cyclin E1 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16023597 736489 Ccne1 cyclin E1 gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:18559482 736489 Ccne1 cyclin E1 gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18559482 736489 Ccne1 cyclin E1 gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16023597 736489 Ccne1 cyclin E1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:21944720 736489 Ccne1 cyclin E1 gene MP:0010173 increased mammary gland epithelial cell proliferation IAGP N RGD:5509061 20150625 MGI PMID:18559482 736489 Ccne1 cyclin E1 gene MP:0010241 abnormal aortic arch development IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:16023597 736489 Ccne1 cyclin E1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12941272 736489 Ccne1 cyclin E1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12970191 736489 Ccne1 cyclin E1 gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:16023597 736489 Ccne1 cyclin E1 gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:16023597 736489 Ccne1 cyclin E1 gene MP:0014126 increased mammary gland apoptosis IAGP N RGD:5509061 20160317 MGI PMID:18559482 736489 Ccne1 cyclin E1 gene MP:0014379 decreased excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:21944720 736489 Ccne1 cyclin E1 gene MP:0020551 abnormal postsynaptic density morphology IAGP N RGD:5509061 20180301 MGI PMID:21944720 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0003005 abnormal hippocampal fimbria morphology IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0005440 increased glycogen level IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0008025 brain vacuoles IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0008917 abnormal oligodendrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0010400 increased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0010762 abnormal microglial cell activation IAGP N RGD:5509061 20141003 MGI PMID:24550399 736490 Man2c1 mannosidase, alpha, class 2C, member 1 gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:24550399 736492 Syn3 synapsin III gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20220519 MGI 736492 Syn3 synapsin III gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20211021 MGI 736492 Syn3 synapsin III gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:23280234 736492 Syn3 synapsin III gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 736492 Syn3 synapsin III gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20190502 MGI 736492 Syn3 synapsin III gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20211021 MGI 736492 Syn3 synapsin III gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 736492 Syn3 synapsin III gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:12040043 736492 Syn3 synapsin III gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220519 MGI 736492 Syn3 synapsin III gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12040043 736492 Syn3 synapsin III gene MP:0002946 delayed axon extension IAGP N RGD:5509061 20141003 MGI PMID:12040043 736492 Syn3 synapsin III gene MP:0002969 impaired social transmission of food preference IAGP N RGD:5509061 20141003 MGI PMID:23280234 736492 Syn3 synapsin III gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 736492 Syn3 synapsin III gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:23280234 736492 Syn3 synapsin III gene MP:0003928 increased heart rate variability IEA N RGD:5509061 20211021 MGI 736492 Syn3 synapsin III gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20151224 MGI PMID:21621590 736492 Syn3 synapsin III gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20151224 MGI PMID:21621590 736492 Syn3 synapsin III gene MP:0005633 increased circulating sodium level IEA N RGD:5509061 20220519 MGI 736492 Syn3 synapsin III gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20151224 MGI PMID:21621590 736492 Syn3 synapsin III gene MP:0010052 increased grip strength IEA N RGD:5509061 20231207 MGI 736492 Syn3 synapsin III gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 736492 Syn3 synapsin III gene MP:0011269 increased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:12040043 736492 Syn3 synapsin III gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20210826 MGI 736497 Mapt microtubule-associated protein tau gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17341679 736497 Mapt microtubule-associated protein tau gene MP:0000604 amyloidosis IAGP N RGD:5509061 20141003 MGI PMID:19041304 736497 Mapt microtubule-associated protein tau gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15069197 736497 Mapt microtubule-associated protein tau gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:20130183 736497 Mapt microtubule-associated protein tau gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20181220 MGI PMID:29911180 736497 Mapt microtubule-associated protein tau gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:19424149 736497 Mapt microtubule-associated protein tau gene MP:0000846 abnormal medulla oblongata morphology IAGP N RGD:5509061 20141003 MGI PMID:17475798 736497 Mapt microtubule-associated protein tau gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20335457 736497 Mapt microtubule-associated protein tau gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20170223 MGI PMID:26842965 736497 Mapt microtubule-associated protein tau gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:19421194 736497 Mapt microtubule-associated protein tau gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20170223 MGI PMID:26842965 736497 Mapt microtubule-associated protein tau gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:21281813 736497 Mapt microtubule-associated protein tau gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15836427 736497 Mapt microtubule-associated protein tau gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15836427 736497 Mapt microtubule-associated protein tau gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15836427 736497 Mapt microtubule-associated protein tau gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:24210822 736497 Mapt microtubule-associated protein tau gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20160128 MGI PMID:26418744 736497 Mapt microtubule-associated protein tau gene MP:0000969 abnormal nociceptor morphology IAGP N RGD:5509061 20160128 MGI PMID:26418744 736497 Mapt microtubule-associated protein tau gene MP:0000972 abnormal mechanoreceptor morphology IAGP N RGD:5509061 20160128 MGI PMID:26418744 736497 Mapt microtubule-associated protein tau gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20170223 MGI PMID:26842965 736497 Mapt microtubule-associated protein tau gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20130183 736497 Mapt microtubule-associated protein tau gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20130183 736497 Mapt microtubule-associated protein tau gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22378884 736497 Mapt microtubule-associated protein tau gene MP:0001265 decreased body size IAGP N RGD:5509061 20230629 MGI PMID:28408410 736497 Mapt microtubule-associated protein tau gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20160421 MGI 736497 Mapt microtubule-associated protein tau gene MP:0001304 cataract IAGP N RGD:5509061 20141003 MGI PMID:15069197 736497 Mapt microtubule-associated protein tau gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20130183 736497 Mapt microtubule-associated protein tau gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20130183 736497 Mapt microtubule-associated protein tau gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22378884 736497 Mapt microtubule-associated protein tau gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20230629 MGI PMID:28408410 736497 Mapt microtubule-associated protein tau gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17341679 736497 Mapt microtubule-associated protein tau gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15069197 736497 Mapt microtubule-associated protein tau gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21492964 736497 Mapt microtubule-associated protein tau gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20869373 736497 Mapt microtubule-associated protein tau gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21281813 736497 Mapt microtubule-associated protein tau gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22378884 736497 Mapt microtubule-associated protein tau gene MP:0001412 excessive scratching IAGP N RGD:5509061 20141003 MGI PMID:15069197 736497 Mapt microtubule-associated protein tau gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 736497 Mapt microtubule-associated protein tau gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22378884 736497 Mapt microtubule-associated protein tau gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:22378884 736497 Mapt microtubule-associated protein tau gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:17478722 736497 Mapt microtubule-associated protein tau gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:19424149 736497 Mapt microtubule-associated protein tau gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:21573167 736497 Mapt microtubule-associated protein tau gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22378884 736497 Mapt microtubule-associated protein tau gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18204444 736497 Mapt microtubule-associated protein tau gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19424149 736497 Mapt microtubule-associated protein tau gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:22378884 736497 Mapt microtubule-associated protein tau gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141204 MGI PMID:24913895 736497 Mapt microtubule-associated protein tau gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:15069197 736497 Mapt microtubule-associated protein tau gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:20130183 736497 Mapt microtubule-associated protein tau gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:15509565 736497 Mapt microtubule-associated protein tau gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:15069197 736497 Mapt microtubule-associated protein tau gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15069197 736497 Mapt microtubule-associated protein tau gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20130183 736497 Mapt microtubule-associated protein tau gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230629 MGI PMID:28408410 736497 Mapt microtubule-associated protein tau gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:22378884 736497 Mapt microtubule-associated protein tau gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20160128 MGI PMID:26418744 736497 Mapt microtubule-associated protein tau gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20869373 736497 Mapt microtubule-associated protein tau gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21281813 736497 Mapt microtubule-associated protein tau gene MP:0002083 premature death IAGP N RGD:5509061 20230629 MGI PMID:28408410 736497 Mapt microtubule-associated protein tau gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:21281813 736497 Mapt microtubule-associated protein tau gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11135642 736497 Mapt microtubule-associated protein tau gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15069197 736497 Mapt microtubule-associated protein tau gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18382274 736497 Mapt microtubule-associated protein tau gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:20130183 736497 Mapt microtubule-associated protein tau gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:19041304 736497 Mapt microtubule-associated protein tau gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:15069197 736497 Mapt microtubule-associated protein tau gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:21281813 736497 Mapt microtubule-associated protein tau gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20160421 MGI 736497 Mapt microtubule-associated protein tau gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141204 MGI PMID:24913895 736497 Mapt microtubule-associated protein tau gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:12859672 736497 Mapt microtubule-associated protein tau gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17475798 736497 Mapt microtubule-associated protein tau gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17478722 736497 Mapt microtubule-associated protein tau gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:20130183 736497 Mapt microtubule-associated protein tau gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:17478722 736497 Mapt microtubule-associated protein tau gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:24210822 736497 Mapt microtubule-associated protein tau gene MP:0002915 abnormal synaptic depression IAGP N RGD:5509061 20170223 MGI PMID:26842965 736497 Mapt microtubule-associated protein tau gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:22378884 736497 Mapt microtubule-associated protein tau gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:17475798 736497 Mapt microtubule-associated protein tau gene MP:0003083 abnormal tibialis anterior morphology IAGP N RGD:5509061 20170223 MGI PMID:26842965 736497 Mapt microtubule-associated protein tau gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20200514 MGI PMID:31160584 736497 Mapt microtubule-associated protein tau gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20335457 736497 Mapt microtubule-associated protein tau gene MP:0003214 neurofibrillary tangles IAGP N RGD:5509061 20141003 MGI PMID:21281813 736497 Mapt microtubule-associated protein tau gene MP:0003214 neurofibrillary tangles IAGP N RGD:5509061 20141003 MGI PMID:21573167 736497 Mapt microtubule-associated protein tau gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:20130183 736497 Mapt microtubule-associated protein tau gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20141003 MGI PMID:17478722 736497 Mapt microtubule-associated protein tau gene MP:0003329 amyloid beta deposits IAGP N RGD:5509061 20200514 MGI PMID:31160584 736497 Mapt microtubule-associated protein tau gene MP:0003354 astrocytosis IAGP N RGD:5509061 20170223 MGI PMID:26842965 736497 Mapt microtubule-associated protein tau gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:24267650 736497 Mapt microtubule-associated protein tau gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20170223 MGI PMID:26842965 736497 Mapt microtubule-associated protein tau gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:11228161 736497 Mapt microtubule-associated protein tau gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:15836427 736497 Mapt microtubule-associated protein tau gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:17341679 736497 Mapt microtubule-associated protein tau gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20160128 MGI PMID:26418744 736497 Mapt microtubule-associated protein tau gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20170223 MGI PMID:26842965 736497 Mapt microtubule-associated protein tau gene MP:0004250 tau protein deposits IAGP N RGD:5509061 20141003 MGI PMID:12859672 736497 Mapt microtubule-associated protein tau gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:22378884 736497 Mapt microtubule-associated protein tau gene MP:0004768 abnormal axonal transport IAGP N RGD:5509061 20141003 MGI PMID:21492964 736497 Mapt microtubule-associated protein tau gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20230629 MGI PMID:28408410 736497 Mapt microtubule-associated protein tau gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:15069197 736497 Mapt microtubule-associated protein tau gene MP:0005277 abnormal brainstem morphology IAGP N RGD:5509061 20141003 MGI PMID:17475798 736497 Mapt microtubule-associated protein tau gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:19041304 736497 Mapt microtubule-associated protein tau gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:17558294 736497 Mapt microtubule-associated protein tau gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:8202139 736497 Mapt microtubule-associated protein tau gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20160128 MGI PMID:26418744 736497 Mapt microtubule-associated protein tau gene MP:0006006 increased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:17475798 736497 Mapt microtubule-associated protein tau gene MP:0006082 CNS inflammation IAGP N RGD:5509061 20200514 MGI PMID:31160584 736497 Mapt microtubule-associated protein tau gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:11228161 736497 Mapt microtubule-associated protein tau gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:17341679 736497 Mapt microtubule-associated protein tau gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:20130183 736497 Mapt microtubule-associated protein tau gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:19424149 736497 Mapt microtubule-associated protein tau gene MP:0008282 enlarged hippocampus IAGP N RGD:5509061 20141003 MGI PMID:17341679 736497 Mapt microtubule-associated protein tau gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:19424149 736497 Mapt microtubule-associated protein tau gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19041304 736497 Mapt microtubule-associated protein tau gene MP:0008486 decreased muscle spindle number IAGP N RGD:5509061 20141003 MGI PMID:15836427 736497 Mapt microtubule-associated protein tau gene MP:0008528 polycystic kidney IEA N RGD:5509061 20160811 MGI 736497 Mapt microtubule-associated protein tau gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:24210822 736497 Mapt microtubule-associated protein tau gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20170223 MGI PMID:26842965 736497 Mapt microtubule-associated protein tau gene MP:0008918 microgliosis IAGP N RGD:5509061 20170223 MGI PMID:26842965 736497 Mapt microtubule-associated protein tau gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:20335457 736497 Mapt microtubule-associated protein tau gene MP:0009317 increased follicular lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19041304 736497 Mapt microtubule-associated protein tau gene MP:0009434 paraparesis IAGP N RGD:5509061 20170223 MGI PMID:26842965 736497 Mapt microtubule-associated protein tau gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19424149 736497 Mapt microtubule-associated protein tau gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141204 MGI PMID:24913895 736497 Mapt microtubule-associated protein tau gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141204 MGI PMID:24913895 736497 Mapt microtubule-associated protein tau gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17475798 736497 Mapt microtubule-associated protein tau gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17478722 736497 Mapt microtubule-associated protein tau gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17341679 736497 Mapt microtubule-associated protein tau gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19424149 736497 Mapt microtubule-associated protein tau gene MP:0010053 decreased grip strength IEA N RGD:5509061 20181227 MGI 736497 Mapt microtubule-associated protein tau gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20160421 MGI 736497 Mapt microtubule-associated protein tau gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20130183 736497 Mapt microtubule-associated protein tau gene MP:0011941 increased fluid intake IEA N RGD:5509061 20211021 MGI 736497 Mapt microtubule-associated protein tau gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210826 MGI 736497 Mapt microtubule-associated protein tau gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20141204 MGI PMID:24913895 736497 Mapt microtubule-associated protein tau gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:19041304 736497 Mapt microtubule-associated protein tau gene MP:0012468 decreased striatum size IAGP N RGD:5509061 20161222 MGI PMID:20130183 736497 Mapt microtubule-associated protein tau gene MP:0014347 increased spleen B cell follicle size IAGP N RGD:5509061 20240104 MGI PMID:19041304 736497 Mapt microtubule-associated protein tau gene MP:0014351 abnormal spleen B cell follicle shape IAGP N RGD:5509061 20240104 MGI PMID:19041304 736497 Mapt microtubule-associated protein tau gene MP:0014368 enhanced long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:17341679 736500 Chp1 calcineurin-like EF hand protein 1 gene MP:0000367 abnormal coat/ hair morphology IEA N RGD:5509061 20230119 MGI 736500 Chp1 calcineurin-like EF hand protein 1 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23904602 736500 Chp1 calcineurin-like EF hand protein 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:23904602 736500 Chp1 calcineurin-like EF hand protein 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:23904602 736500 Chp1 calcineurin-like EF hand protein 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230119 MGI 736500 Chp1 calcineurin-like EF hand protein 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 736500 Chp1 calcineurin-like EF hand protein 1 gene MP:0003225 axonal dystrophy IAGP N RGD:5509061 20141003 MGI PMID:23904602 736500 Chp1 calcineurin-like EF hand protein 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230119 MGI 736500 Chp1 calcineurin-like EF hand protein 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:23904602 736500 Chp1 calcineurin-like EF hand protein 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20230119 MGI 736500 Chp1 calcineurin-like EF hand protein 1 gene MP:0008571 abnormal synaptic bouton morphology IAGP N RGD:5509061 20141003 MGI PMID:23904602 736500 Chp1 calcineurin-like EF hand protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 736500 Chp1 calcineurin-like EF hand protein 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20230119 MGI 736500 Chp1 calcineurin-like EF hand protein 1 gene MP:0014329 abnormal Purkinje cell axon morphology IAGP N RGD:5509061 20240118 MGI PMID:23904602 736502 Sstr5 somatostatin receptor 5 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12511609 736502 Sstr5 somatostatin receptor 5 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20200514 MGI 736502 Sstr5 somatostatin receptor 5 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15919085 736502 Sstr5 somatostatin receptor 5 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:12511609 736502 Sstr5 somatostatin receptor 5 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12511609 736502 Sstr5 somatostatin receptor 5 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12511609 736502 Sstr5 somatostatin receptor 5 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:12035032 736502 Sstr5 somatostatin receptor 5 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:12511609 736502 Sstr5 somatostatin receptor 5 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15919085 736502 Sstr5 somatostatin receptor 5 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:12035032 736502 Sstr5 somatostatin receptor 5 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15919085 736502 Sstr5 somatostatin receptor 5 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:15223137 736502 Sstr5 somatostatin receptor 5 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:12035032 736502 Sstr5 somatostatin receptor 5 gene MP:0003839 abnormal insulin clearance IAGP N RGD:5509061 20141003 MGI PMID:15919085 736502 Sstr5 somatostatin receptor 5 gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12035032 736502 Sstr5 somatostatin receptor 5 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12511609 736502 Sstr5 somatostatin receptor 5 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15919085 736502 Sstr5 somatostatin receptor 5 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12035032 736502 Sstr5 somatostatin receptor 5 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12035032 736502 Sstr5 somatostatin receptor 5 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12511609 736502 Sstr5 somatostatin receptor 5 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15919085 736502 Sstr5 somatostatin receptor 5 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12511609 736502 Sstr5 somatostatin receptor 5 gene MP:0009181 decreased pancreatic delta cell number IAGP N RGD:5509061 20141003 MGI PMID:15919085 736506 Acp3 acid phosphatase 3 gene MP:0001168 abnormal prostate gland epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24039861 736506 Acp3 acid phosphatase 3 gene MP:0003177 allodynia IAGP N RGD:5509061 20141003 MGI PMID:18940592 736506 Acp3 acid phosphatase 3 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:18940592 736506 Acp3 acid phosphatase 3 gene MP:0009219 increased prostate intraepithelial neoplasia incidence IAGP N RGD:5509061 20141003 MGI PMID:24039861 736506 Acp3 acid phosphatase 3 gene MP:0009220 increased prostate gland adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:24039861 736506 Acp3 acid phosphatase 3 gene MP:0009381 abnormal prostate gland dorsolateral lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:24039861 736506 Acp3 acid phosphatase 3 gene MP:0031369 prostate gland dorsolateral lobe hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:24039861 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000243 myoclonus IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:18791226 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19261867 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000745 tremors IAGP N RGD:5509061 20160526 MGI PMID:26807988 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000745 tremors IAGP N RGD:5509061 20181220 MGI PMID:12204355 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:18791226 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000747 muscle weakness IAGP N RGD:5509061 20160526 MGI PMID:26807988 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:4315332 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000749 muscle degeneration IAGP N RGD:5509061 20141003 MGI PMID:11532991 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000751 myopathy IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000752 dystrophic muscle IAGP N RGD:5509061 20141003 MGI PMID:11532991 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:12374766 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:11532991 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:12955145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:15170223 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:15286995 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:18791226 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:19261867 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:7601440 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000872 abnormal cerebellum external granule cell layer morphology IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000876 Purkinje cell degeneration IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:6127695 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:6319212 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20170420 MGI PMID:28355569 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0000958 peripheral nervous system degeneration IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:4315332 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20170420 MGI PMID:28355569 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11532991 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7601440 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160526 MGI PMID:26807988 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19254928 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:19254928 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12374766 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15286995 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18791226 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19261867 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001393 ataxia IAGP N RGD:5509061 20160526 MGI PMID:26807988 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20160526 MGI PMID:26807988 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:18791226 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19254928 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160526 MGI PMID:26807988 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001485 abnormal pinna reflex IAGP N RGD:5509061 20171228 MGI PMID:20057387 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20171228 MGI PMID:20057387 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001504 abnormal posture IAGP N RGD:5509061 20181220 MGI PMID:12204355 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:7601440 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20150521 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001524 impaired limb coordination IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:7601440 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001891 hydrocephaly IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11532991 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:24288358 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20160526 MGI PMID:26807988 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:11532991 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:18791226 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19254928 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19261867 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:4315332 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11532991 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12374766 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15170223 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15286995 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18791226 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19254928 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19261867 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24288358 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7601440 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002083 premature death IAGP N RGD:5509061 20160526 MGI PMID:26807988 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:4323310 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002152 abnormal brain morphology IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20181220 MGI PMID:12204355 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:12374766 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:15170223 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:4315332 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:7601440 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002272 abnormal nervous system electrophysiology IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002687 oligozoospermia IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:17881658 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:21156207 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20141003 MGI PMID:4323310 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0003157 impaired muscle relaxation IEA N RGD:5509061 20160609 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20141003 MGI PMID:11532991 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0003852 skeletal muscle necrosis IAGP N RGD:5509061 20141003 MGI PMID:11532991 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0003993 abnormal ventral spinal root morphology IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0004142 abnormal muscle tone IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:11532991 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0004709 cervical vertebrae degeneration IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0004748 increased susceptibility to age-related hearing loss IAGP N RGD:5509061 20181220 MGI PMID:12204355 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20160526 MGI PMID:26807988 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:4323310 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:24288358 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210826 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11532991 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0005307 head tossing IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:12374766 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0005323 dystonia IAGP N RGD:5509061 20141003 MGI PMID:18791226 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0005323 dystonia IAGP N RGD:5509061 20160526 MGI PMID:26807988 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:4323310 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20181220 MGI PMID:12204355 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:6127695 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0005405 axon degeneration IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15901786 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16822974 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18791226 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141003 MGI PMID:11532991 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0006325 impaired hearing IAGP N RGD:5509061 20181220 MGI PMID:12204355 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0006358 absent pinna reflex IAGP N RGD:5509061 20171228 MGI PMID:20057387 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:21156207 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20160526 MGI PMID:26807988 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20170420 MGI PMID:28355569 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:17881658 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:19254928 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0008924 decreased cerebellar granule cell number IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0009400 decreased skeletal muscle fiber size IEA N RGD:5509061 20111116 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20170420 MGI PMID:28355569 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0009434 paraparesis IAGP N RGD:5509061 20181220 MGI PMID:12204355 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0009779 enhanced behavioral response to anesthetic IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20160526 MGI PMID:26807988 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0010492 abnormal atrium endocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:11532991 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12955145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15170223 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17881658 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21156207 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0011380 enlarged brain ventricles IEA N RGD:5509061 20141003 MGI 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:19737145 736507 Scn8a sodium channel, voltage-gated, type VIII, alpha gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20171228 MGI PMID:20057387 736509 Gnb2 guanine nucleotide binding protein (G protein), beta 2 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20230601 MGI 736509 Gnb2 guanine nucleotide binding protein (G protein), beta 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 736509 Gnb2 guanine nucleotide binding protein (G protein), beta 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20201022 MGI 736509 Gnb2 guanine nucleotide binding protein (G protein), beta 2 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210520 MGI 736509 Gnb2 guanine nucleotide binding protein (G protein), beta 2 gene MP:0002626 increased heart rate IEA N RGD:5509061 20181227 MGI 736509 Gnb2 guanine nucleotide binding protein (G protein), beta 2 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20220811 MGI 736509 Gnb2 guanine nucleotide binding protein (G protein), beta 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20220811 MGI 736509 Gnb2 guanine nucleotide binding protein (G protein), beta 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20230601 MGI 736509 Gnb2 guanine nucleotide binding protein (G protein), beta 2 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20220811 MGI 736509 Gnb2 guanine nucleotide binding protein (G protein), beta 2 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20220811 MGI 736509 Gnb2 guanine nucleotide binding protein (G protein), beta 2 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20220811 MGI 736509 Gnb2 guanine nucleotide binding protein (G protein), beta 2 gene MP:0010507 shortened RR interval IEA N RGD:5509061 20181227 MGI 736509 Gnb2 guanine nucleotide binding protein (G protein), beta 2 gene MP:0010571 shortened ST segment IEA N RGD:5509061 20181227 MGI 736509 Gnb2 guanine nucleotide binding protein (G protein), beta 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 736510 Mgat3 mannoside acetylglucosaminyltransferase 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9061364 736510 Mgat3 mannoside acetylglucosaminyltransferase 3 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20141003 MGI PMID:14633700 736510 Mgat3 mannoside acetylglucosaminyltransferase 3 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:14633700 736510 Mgat3 mannoside acetylglucosaminyltransferase 3 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:14633700 736510 Mgat3 mannoside acetylglucosaminyltransferase 3 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:9661906 736510 Mgat3 mannoside acetylglucosaminyltransferase 3 gene MP:0005517 impaired liver regeneration IAGP N RGD:5509061 20141003 MGI PMID:14633700 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0002901 increased urine phosphate level IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0002905 decreased circulating parathyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0003116 rickets IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0003197 nephrocalcinosis IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:9560283 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0010110 abnormal renal phosphate reabsorption IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:19570882 736512 Slc34a1 solute carrier family 34 (sodium phosphate), member 1 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:9560283 736514 Pvr poliovirus receptor gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:17621371 736514 Pvr poliovirus receptor gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:17621371 736514 Pvr poliovirus receptor gene MP:0002079 increased circulating insulin level IEA N RGD:5509061 20211021 MGI 736514 Pvr poliovirus receptor gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:18973187 736514 Pvr poliovirus receptor gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:17621371 736514 Pvr poliovirus receptor gene MP:0005358 abnormal incisor morphology IEA N RGD:5509061 20210128 MGI 736514 Pvr poliovirus receptor gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:17621371 736514 Pvr poliovirus receptor gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:17621371 736514 Pvr poliovirus receptor gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:17621371 736514 Pvr poliovirus receptor gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18973187 736516 Esyt1 extended synaptotagmin-like protein 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20230601 MGI 736516 Esyt1 extended synaptotagmin-like protein 1 gene MP:0002100 abnormal tooth morphology IEA N RGD:5509061 20230601 MGI 736516 Esyt1 extended synaptotagmin-like protein 1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20150528 MGI 736516 Esyt1 extended synaptotagmin-like protein 1 gene MP:0012121 sclerocornea IEA N RGD:5509061 20230601 MGI 736516 Esyt1 extended synaptotagmin-like protein 1 gene MP:0012122 abnormal iris transillumination IEA N RGD:5509061 20230601 MGI 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9580260 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15673679 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:15673679 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:15673679 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:11182093 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:17620617 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11182092 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:11182093 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0002886 abnormal glutamate-mediated receptor currents IAGP N RGD:5509061 20141003 MGI PMID:9580260 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:9580260 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:11182093 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:11182093 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:11182092 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:17620617 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:11144357 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:15673679 736517 Grik2 glutamate receptor, ionotropic, kainate 2 (beta 2) gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:11182093 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0000035 abnormal membranous labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:9682811 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:15855646 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:9682811 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20160421 MGI 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20847057 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24262794 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002083 premature death IAGP N RGD:5509061 20191212 MGI PMID:29263159 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:11447218 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20191212 MGI PMID:29263159 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002607 decreased basophil cell number IEA N RGD:5509061 20210128 MGI 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002704 tubular nephritis IAGP N RGD:5509061 20141003 MGI PMID:11447218 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:10880400 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:20847057 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002871 albuminuria IAGP N RGD:5509061 20191212 MGI PMID:29263159 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20210128 MGI 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:20847057 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:24262794 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0003215 renal interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:20847057 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:11073824 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0003606 kidney failure IAGP N RGD:5509061 20191212 MGI PMID:29263159 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0004366 abnormal strial marginal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9682811 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0004368 abnormal stria vascularis vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9682811 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0004598 abnormal cochlear basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:15855646 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0004598 abnormal cochlear basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:9682811 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:9682811 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:20847057 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005161 hematuria IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:24262794 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20191212 MGI PMID:29263159 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:20847057 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:20847057 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20191212 MGI PMID:29263159 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0005568 increased circulating total protein level IAGP N RGD:5509061 20141003 MGI PMID:11073824 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:24262794 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:20847057 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:9682811 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20191212 MGI PMID:29263159 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0008805 decreased circulating amylase level IEA N RGD:5509061 20181227 MGI 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0009644 uremia IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:20847057 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011346 renal tubule atrophy IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:10880400 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11073824 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:24262794 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20191212 MGI PMID:29263159 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011349 abnormal renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:20847057 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011349 abnormal renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:24262794 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:10880400 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:24262794 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011437 glomerulus hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20197625 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011506 glomerular crescent IAGP N RGD:5509061 20191212 MGI PMID:29263159 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011534 granular kidney IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011868 podocyte microvillus transformation IAGP N RGD:5509061 20141003 MGI PMID:8956999 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:8947561 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:9682811 736519 Col4a3 collagen, type IV, alpha 3 gene MP:0012362 increased large unstained cell number IEA N RGD:5509061 20231207 MGI 736520 mt-Nd2 NADH dehydrogenase 2, mitochondrial gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141106 MGI PMID:15692809 736520 mt-Nd2 NADH dehydrogenase 2, mitochondrial gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141106 MGI PMID:17189252 736520 mt-Nd2 NADH dehydrogenase 2, mitochondrial gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141106 MGI PMID:17189252 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20210520 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20201022 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0001126 abnormal ovary morphology IEA N RGD:5509061 20201022 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210520 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20201022 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0002188 small heart IEA N RGD:5509061 20201022 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20201022 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0002989 small kidney IEA N RGD:5509061 20201022 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20240404 MGI PMID:35661710 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20210826 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20210826 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0009342 enlarged gallbladder IEA N RGD:5509061 20210826 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240404 MGI PMID:35661710 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20200310 MGI 736521 Cand1 cullin associated and neddylation disassociated 1 gene MP:0020344 abnormal susceptibility to injury induced morbidity/mortality IAGP N RGD:5509061 20240404 MGI PMID:35661710 736523 Slc16a7 solute carrier family 16 (monocarboxylic acid transporters), member 7 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20201210 MGI PMID:32693190 736523 Slc16a7 solute carrier family 16 (monocarboxylic acid transporters), member 7 gene MP:0011827 impaired neuron differentiation IAGP N RGD:5509061 20201210 MGI PMID:32693190 736523 Slc16a7 solute carrier family 16 (monocarboxylic acid transporters), member 7 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20201210 MGI PMID:32693190 736523 Slc16a7 solute carrier family 16 (monocarboxylic acid transporters), member 7 gene MP:0014064 argyrophilic inclusion bodies IAGP N RGD:5509061 20201210 MGI PMID:32693190 736523 Slc16a7 solute carrier family 16 (monocarboxylic acid transporters), member 7 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:32693190 736524 Hmgb2 high mobility group box 2 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:11262228 736524 Hmgb2 high mobility group box 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11262228 736524 Hmgb2 high mobility group box 2 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11262228 736524 Hmgb2 high mobility group box 2 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:11262228 736524 Hmgb2 high mobility group box 2 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11262228 736524 Hmgb2 high mobility group box 2 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11262228 736524 Hmgb2 high mobility group box 2 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11262228 736524 Hmgb2 high mobility group box 2 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20180301 MGI PMID:11262228 736527 Runx1 runt related transcription factor 1 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:20181744 736527 Runx1 runt related transcription factor 1 gene MP:0000158 absent sternum IAGP N RGD:5509061 20141003 MGI PMID:20181744 736527 Runx1 runt related transcription factor 1 gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:20181744 736527 Runx1 runt related transcription factor 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:24095735 736527 Runx1 runt related transcription factor 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17290219 736527 Runx1 runt related transcription factor 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19129762 736527 Runx1 runt related transcription factor 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24095735 736527 Runx1 runt related transcription factor 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15713794 736527 Runx1 runt related transcription factor 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17290219 736527 Runx1 runt related transcription factor 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20139099 736527 Runx1 runt related transcription factor 1 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20210520 MGI PMID:32249213 736527 Runx1 runt related transcription factor 1 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:14966519 736527 Runx1 runt related transcription factor 1 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:10943840 736527 Runx1 runt related transcription factor 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:8622955 736527 Runx1 runt related transcription factor 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10943840 736527 Runx1 runt related transcription factor 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:17994017 736527 Runx1 runt related transcription factor 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19129762 736527 Runx1 runt related transcription factor 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0000402 abnormal zigzag hair morphology IAGP N RGD:5509061 20141003 MGI PMID:17011173 736527 Runx1 runt related transcription factor 1 gene MP:0000404 decreased curvature of zigzag hairs IAGP N RGD:5509061 20141003 MGI PMID:17011173 736527 Runx1 runt related transcription factor 1 gene MP:0000406 increased curvature of auchene hairs IAGP N RGD:5509061 20141003 MGI PMID:17011173 736527 Runx1 runt related transcription factor 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:19129762 736527 Runx1 runt related transcription factor 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:20035012 736527 Runx1 runt related transcription factor 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:20647008 736527 Runx1 runt related transcription factor 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:8565077 736527 Runx1 runt related transcription factor 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:9558367 736527 Runx1 runt related transcription factor 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:15713794 736527 Runx1 runt related transcription factor 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0000696 abnormal Peyer's patch morphology IAGP N RGD:5509061 20141003 MGI PMID:21178013 736527 Runx1 runt related transcription factor 1 gene MP:0000701 abnormal lymph node size IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:14504086 736527 Runx1 runt related transcription factor 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:15713794 736527 Runx1 runt related transcription factor 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:15713794 736527 Runx1 runt related transcription factor 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:17646406 736527 Runx1 runt related transcription factor 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19129762 736527 Runx1 runt related transcription factor 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:21178013 736527 Runx1 runt related transcription factor 1 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:23325226 736527 Runx1 runt related transcription factor 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:23325226 736527 Runx1 runt related transcription factor 1 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20160128 MGI PMID:26418744 736527 Runx1 runt related transcription factor 1 gene MP:0000972 abnormal mechanoreceptor morphology IAGP N RGD:5509061 20160128 MGI PMID:26418744 736527 Runx1 runt related transcription factor 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15713794 736527 Runx1 runt related transcription factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15713794 736527 Runx1 runt related transcription factor 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16081688 736527 Runx1 runt related transcription factor 1 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:17011173 736527 Runx1 runt related transcription factor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16081688 736527 Runx1 runt related transcription factor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:16496309 736527 Runx1 runt related transcription factor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19129762 736527 Runx1 runt related transcription factor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:19570513 736527 Runx1 runt related transcription factor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:20139099 736527 Runx1 runt related transcription factor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22392989 736527 Runx1 runt related transcription factor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23335233 736527 Runx1 runt related transcription factor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20210520 MGI PMID:32249213 736527 Runx1 runt related transcription factor 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15914564 736527 Runx1 runt related transcription factor 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16105979 736527 Runx1 runt related transcription factor 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0001602 impaired myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8622955 736527 Runx1 runt related transcription factor 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:16496309 736527 Runx1 runt related transcription factor 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20647008 736527 Runx1 runt related transcription factor 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8622955 736527 Runx1 runt related transcription factor 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9054947 736527 Runx1 runt related transcription factor 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10943840 736527 Runx1 runt related transcription factor 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19129762 736527 Runx1 runt related transcription factor 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20139099 736527 Runx1 runt related transcription factor 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8565077 736527 Runx1 runt related transcription factor 1 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8622955 736527 Runx1 runt related transcription factor 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17290219 736527 Runx1 runt related transcription factor 1 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:20647008 736527 Runx1 runt related transcription factor 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14504086 736527 Runx1 runt related transcription factor 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15713794 736527 Runx1 runt related transcription factor 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17646406 736527 Runx1 runt related transcription factor 1 gene MP:0001825 arrested T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17994017 736527 Runx1 runt related transcription factor 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:17290219 736527 Runx1 runt related transcription factor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16496309 736527 Runx1 runt related transcription factor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20035012 736527 Runx1 runt related transcription factor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:20647008 736527 Runx1 runt related transcription factor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22392989 736527 Runx1 runt related transcription factor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8622955 736527 Runx1 runt related transcription factor 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9054947 736527 Runx1 runt related transcription factor 1 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10943840 736527 Runx1 runt related transcription factor 1 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15914564 736527 Runx1 runt related transcription factor 1 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17290219 736527 Runx1 runt related transcription factor 1 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8565077 736527 Runx1 runt related transcription factor 1 gene MP:0001917 intraventricular hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9558367 736527 Runx1 runt related transcription factor 1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:12086889 736527 Runx1 runt related transcription factor 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12086889 736527 Runx1 runt related transcription factor 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12499254 736527 Runx1 runt related transcription factor 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16081688 736527 Runx1 runt related transcription factor 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12086889 736527 Runx1 runt related transcription factor 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:22392989 736527 Runx1 runt related transcription factor 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19570513 736527 Runx1 runt related transcription factor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24095735 736527 Runx1 runt related transcription factor 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:20181744 736527 Runx1 runt related transcription factor 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10943840 736527 Runx1 runt related transcription factor 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:14966519 736527 Runx1 runt related transcription factor 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:20035012 736527 Runx1 runt related transcription factor 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9811459 736527 Runx1 runt related transcription factor 1 gene MP:0002123 abnormal definitive hematopoiesis IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14966519 736527 Runx1 runt related transcription factor 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:14966519 736527 Runx1 runt related transcription factor 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16081688 736527 Runx1 runt related transcription factor 1 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11265752 736527 Runx1 runt related transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14630789 736527 Runx1 runt related transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16496309 736527 Runx1 runt related transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20647008 736527 Runx1 runt related transcription factor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8565077 736527 Runx1 runt related transcription factor 1 gene MP:0002239 abnormal nasal septum morphology IAGP N RGD:5509061 20230511 MGI PMID:19000669 736527 Runx1 runt related transcription factor 1 gene MP:0002340 abnormal axillary lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:21178013 736527 Runx1 runt related transcription factor 1 gene MP:0002353 abnormal inguinal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:21178013 736527 Runx1 runt related transcription factor 1 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0002367 abnormal thymus lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0002367 abnormal thymus lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:15713794 736527 Runx1 runt related transcription factor 1 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:12086889 736527 Runx1 runt related transcription factor 1 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20139099 736527 Runx1 runt related transcription factor 1 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22392989 736527 Runx1 runt related transcription factor 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:20139099 736527 Runx1 runt related transcription factor 1 gene MP:0002408 abnormal double-positive T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17646406 736527 Runx1 runt related transcription factor 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14966519 736527 Runx1 runt related transcription factor 1 gene MP:0002413 abnormal megakaryocyte progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20647008 736527 Runx1 runt related transcription factor 1 gene MP:0002414 abnormal myeloblast morphology/development IAGP N RGD:5509061 20141003 MGI PMID:19570513 736527 Runx1 runt related transcription factor 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14966519 736527 Runx1 runt related transcription factor 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15914564 736527 Runx1 runt related transcription factor 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0002450 abnormal lymph organ development IAGP N RGD:5509061 20141003 MGI PMID:21178013 736527 Runx1 runt related transcription factor 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20210520 MGI PMID:32249213 736527 Runx1 runt related transcription factor 1 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15914564 736527 Runx1 runt related transcription factor 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:20181744 736527 Runx1 runt related transcription factor 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:23325226 736527 Runx1 runt related transcription factor 1 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:14966519 736527 Runx1 runt related transcription factor 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17290219 736527 Runx1 runt related transcription factor 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:17994017 736527 Runx1 runt related transcription factor 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20139099 736527 Runx1 runt related transcription factor 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:24095735 736527 Runx1 runt related transcription factor 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20190131 MGI PMID:30322915 736527 Runx1 runt related transcription factor 1 gene MP:0003227 abnormal vascular branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:10943840 736527 Runx1 runt related transcription factor 1 gene MP:0003279 aneurysm IAGP N RGD:5509061 20141003 MGI PMID:10943840 736527 Runx1 runt related transcription factor 1 gene MP:0003279 aneurysm IAGP N RGD:5509061 20141003 MGI PMID:20647008 736527 Runx1 runt related transcription factor 1 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10226014 736527 Runx1 runt related transcription factor 1 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15914564 736527 Runx1 runt related transcription factor 1 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17290219 736527 Runx1 runt related transcription factor 1 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8565077 736527 Runx1 runt related transcription factor 1 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9558367 736527 Runx1 runt related transcription factor 1 gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:23335233 736527 Runx1 runt related transcription factor 1 gene MP:0003719 abnormal pericyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20647008 736527 Runx1 runt related transcription factor 1 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:14504086 736527 Runx1 runt related transcription factor 1 gene MP:0004049 increased acute promyelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:12086889 736527 Runx1 runt related transcription factor 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:10943840 736527 Runx1 runt related transcription factor 1 gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20190131 MGI PMID:30322915 736527 Runx1 runt related transcription factor 1 gene MP:0004720 abnormal platelet morphology IAGP N RGD:5509061 20141003 MGI PMID:19129762 736527 Runx1 runt related transcription factor 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:20139099 736527 Runx1 runt related transcription factor 1 gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19129762 736527 Runx1 runt related transcription factor 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19129762 736527 Runx1 runt related transcription factor 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19570513 736527 Runx1 runt related transcription factor 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20139099 736527 Runx1 runt related transcription factor 1 gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20210520 MGI PMID:32249213 736527 Runx1 runt related transcription factor 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19129762 736527 Runx1 runt related transcription factor 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19570513 736527 Runx1 runt related transcription factor 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:20035012 736527 Runx1 runt related transcription factor 1 gene MP:0004938 dilated vasculature IAGP N RGD:5509061 20141003 MGI PMID:20647008 736527 Runx1 runt related transcription factor 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17994017 736527 Runx1 runt related transcription factor 1 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:17994017 736527 Runx1 runt related transcription factor 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15713794 736527 Runx1 runt related transcription factor 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17290219 736527 Runx1 runt related transcription factor 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19129762 736527 Runx1 runt related transcription factor 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24095735 736527 Runx1 runt related transcription factor 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17994017 736527 Runx1 runt related transcription factor 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19129762 736527 Runx1 runt related transcription factor 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19570513 736527 Runx1 runt related transcription factor 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17994017 736527 Runx1 runt related transcription factor 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17646406 736527 Runx1 runt related transcription factor 1 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:17994017 736527 Runx1 runt related transcription factor 1 gene MP:0005091 increased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16081688 736527 Runx1 runt related transcription factor 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17646406 736527 Runx1 runt related transcription factor 1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19129762 736527 Runx1 runt related transcription factor 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:10943840 736527 Runx1 runt related transcription factor 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:17290219 736527 Runx1 runt related transcription factor 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:8565077 736527 Runx1 runt related transcription factor 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:8622955 736527 Runx1 runt related transcription factor 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:9558367 736527 Runx1 runt related transcription factor 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20160128 MGI PMID:26418744 736527 Runx1 runt related transcription factor 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:17290219 736527 Runx1 runt related transcription factor 1 gene MP:0005435 hemoperitoneum IAGP N RGD:5509061 20141003 MGI PMID:8565077 736527 Runx1 runt related transcription factor 1 gene MP:0005460 abnormal leukopoiesis IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:20181744 736527 Runx1 runt related transcription factor 1 gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12086889 736527 Runx1 runt related transcription factor 1 gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0006208 lethality throughout fetal growth and development IAGP N RGD:5509061 20230511 MGI PMID:19000669 736527 Runx1 runt related transcription factor 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14966519 736527 Runx1 runt related transcription factor 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19129762 736527 Runx1 runt related transcription factor 1 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20647008 736527 Runx1 runt related transcription factor 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:14504086 736527 Runx1 runt related transcription factor 1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18258917 736527 Runx1 runt related transcription factor 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16081688 736527 Runx1 runt related transcription factor 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17290219 736527 Runx1 runt related transcription factor 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17646406 736527 Runx1 runt related transcription factor 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18258917 736527 Runx1 runt related transcription factor 1 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21178013 736527 Runx1 runt related transcription factor 1 gene MP:0008076 abnormal CD4-positive T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17646406 736527 Runx1 runt related transcription factor 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16081688 736527 Runx1 runt related transcription factor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:17646406 736527 Runx1 runt related transcription factor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:18258917 736527 Runx1 runt related transcription factor 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0008080 abnormal CD8-positive, alpha-beta T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17646406 736527 Runx1 runt related transcription factor 1 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0008111 abnormal granulocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:16081688 736527 Runx1 runt related transcription factor 1 gene MP:0008133 decreased Peyer's patch number IAGP N RGD:5509061 20141003 MGI PMID:21178013 736527 Runx1 runt related transcription factor 1 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:21178013 736527 Runx1 runt related transcription factor 1 gene MP:0008186 increased pro-B cell number IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0008246 abnormal leukocyte morphology IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0008555 abnormal interferon secretion IAGP N RGD:5509061 20141003 MGI PMID:18258917 736527 Runx1 runt related transcription factor 1 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:20139099 736527 Runx1 runt related transcription factor 1 gene MP:0008801 abnormal erythroid progenitor cell morphology IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:20647008 736527 Runx1 runt related transcription factor 1 gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20210520 MGI PMID:32249213 736527 Runx1 runt related transcription factor 1 gene MP:0008986 abnormal liver parenchyma morphology IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0009253 abnormal sympathetic neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:23325226 736527 Runx1 runt related transcription factor 1 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19647224 736527 Runx1 runt related transcription factor 1 gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20210520 MGI PMID:32249213 736527 Runx1 runt related transcription factor 1 gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8622955 736527 Runx1 runt related transcription factor 1 gene MP:0009541 increased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20190131 MGI PMID:30322915 736527 Runx1 runt related transcription factor 1 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20230511 MGI PMID:19000669 736527 Runx1 runt related transcription factor 1 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20210520 MGI PMID:32249213 736527 Runx1 runt related transcription factor 1 gene MP:0010178 increased number of Howell-Jolly bodies IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17290219 736527 Runx1 runt related transcription factor 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15713794 736527 Runx1 runt related transcription factor 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17290219 736527 Runx1 runt related transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15914564 736527 Runx1 runt related transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16496309 736527 Runx1 runt related transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17290219 736527 Runx1 runt related transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20035012 736527 Runx1 runt related transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22392989 736527 Runx1 runt related transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23335233 736527 Runx1 runt related transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8565077 736527 Runx1 runt related transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8622955 736527 Runx1 runt related transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9054947 736527 Runx1 runt related transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9558367 736527 Runx1 runt related transcription factor 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9811459 736527 Runx1 runt related transcription factor 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20647008 736527 Runx1 runt related transcription factor 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20181744 736527 Runx1 runt related transcription factor 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19129762 736527 Runx1 runt related transcription factor 1 gene MP:0011180 abnormal hematopoietic cell number IAGP N RGD:5509061 20141003 MGI PMID:23335233 736527 Runx1 runt related transcription factor 1 gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20141003 MGI PMID:20647008 736527 Runx1 runt related transcription factor 1 gene MP:0011816 decreased pre-pro B cell number IAGP N RGD:5509061 20150219 MGI PMID:23823022 736527 Runx1 runt related transcription factor 1 gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16247465 736527 Runx1 runt related transcription factor 1 gene MP:0013241 embryo tissue necrosis IAGP N RGD:5509061 20141003 MGI PMID:8622955 736527 Runx1 runt related transcription factor 1 gene MP:0013657 abnormal blood cell morphology IAGP N RGD:5509061 20190131 MGI PMID:30322915 736527 Runx1 runt related transcription factor 1 gene MP:0013658 abnormal myeloid cell morphology IAGP N RGD:5509061 20190131 MGI PMID:30322915 736527 Runx1 runt related transcription factor 1 gene MP:0013658 abnormal myeloid cell morphology IAGP N RGD:5509061 20210520 MGI PMID:32249213 736527 Runx1 runt related transcription factor 1 gene MP:0013659 abnormal erythroid lineage cell morphology IAGP N RGD:5509061 20190131 MGI PMID:30322915 736527 Runx1 runt related transcription factor 1 gene MP:0013663 increased myeloid cell number IAGP N RGD:5509061 20190131 MGI PMID:30322915 736527 Runx1 runt related transcription factor 1 gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:20181744 736527 Runx1 runt related transcription factor 1 gene MP:0014130 thymus cyst IAGP N RGD:5509061 20160324 MGI PMID:17626615 736527 Runx1 runt related transcription factor 1 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:12086889 736527 Runx1 runt related transcription factor 1 gene MP:0021212 abnormal primary and secondary palatal fusion IAGP N RGD:5509061 20230511 MGI PMID:19000669 736527 Runx1 runt related transcription factor 1 gene MP:0021214 anterior cleft palate IAGP N RGD:5509061 20230511 MGI PMID:19000669 736527 Runx1 runt related transcription factor 1 gene MP:0031460 abnormal palatal shelf morphology IAGP N RGD:5509061 20230511 MGI PMID:19000669 736528 Atp5f1e ATP synthase F1 subunit epsilon gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230720 MGI 736528 Atp5f1e ATP synthase F1 subunit epsilon gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230720 MGI 736528 Atp5f1e ATP synthase F1 subunit epsilon gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230720 MGI 736528 Atp5f1e ATP synthase F1 subunit epsilon gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20230720 MGI 736529 Gucy2c guanylate cyclase 2c gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:21865642 736529 Gucy2c guanylate cyclase 2c gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:21865642 736529 Gucy2c guanylate cyclase 2c gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21865642 736529 Gucy2c guanylate cyclase 2c gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21865642 736529 Gucy2c guanylate cyclase 2c gene MP:0002409 decreased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:9344852 736529 Gucy2c guanylate cyclase 2c gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9294128 736529 Gucy2c guanylate cyclase 2c gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:21865642 736529 Gucy2c guanylate cyclase 2c gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:21865642 736529 Gucy2c guanylate cyclase 2c gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:9294128 736529 Gucy2c guanylate cyclase 2c gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21865642 736529 Gucy2c guanylate cyclase 2c gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:21865642 736529 Gucy2c guanylate cyclase 2c gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21865642 736529 Gucy2c guanylate cyclase 2c gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9294128 736529 Gucy2c guanylate cyclase 2c gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21865642 736529 Gucy2c guanylate cyclase 2c gene MP:0010934 increased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21865642 736529 Gucy2c guanylate cyclase 2c gene MP:0011958 increased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:21865642 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20160218 MGI PMID:25048459 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20161208 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20160218 MGI PMID:25048459 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20181227 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20181227 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20181227 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0000741 impaired contractility of urinary bladder detrusor smooth muscle IAGP N RGD:5509061 20181025 MGI PMID:19484501 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20231207 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0001756 abnormal urination IAGP N RGD:5509061 20181025 MGI PMID:19484501 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20160218 MGI PMID:25048459 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20160218 MGI PMID:25048459 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20231207 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0002708 nephrolithiasis IAGP N RGD:5509061 20181025 MGI PMID:19484501 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0002989 small kidney IEA N RGD:5509061 20181227 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20181227 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20160218 MGI PMID:25048459 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0003587 ureter obstruction IAGP N RGD:5509061 20160218 MGI PMID:25048459 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0003587 ureter obstruction IAGP N RGD:5509061 20181025 MGI PMID:19484501 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20211021 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20231207 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210128 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20231207 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0005360 urolithiasis IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20160218 MGI PMID:25048459 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20161208 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0008528 polycystic kidney IEA N RGD:5509061 20181227 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0009552 urinary bladder obstruction IAGP N RGD:5509061 20160218 MGI PMID:25048459 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0009644 uremia IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0009645 crystalluria IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20231207 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20181025 MGI PMID:19484501 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20161208 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0011422 kidney medulla atrophy IAGP N RGD:5509061 20161208 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0011468 abnormal urine amino acid level IAGP N RGD:5509061 20141003 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0011625 cystolithiasis IAGP N RGD:5509061 20160218 MGI PMID:25048459 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0011625 cystolithiasis IAGP N RGD:5509061 20181025 MGI PMID:19484501 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0011625 cystolithiasis IAGP N RGD:5509061 20181025 MGI PMID:28165480 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0011774 abnormal urinary bladder detrusor smooth muscle morphology IAGP N RGD:5509061 20181025 MGI PMID:19484501 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0011799 increased urinary bladder weight IAGP N RGD:5509061 20181025 MGI PMID:19484501 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20181227 MGI 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0011923 abnormal bladder urine volume IAGP N RGD:5509061 20181025 MGI PMID:19484501 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0020400 cystinuria IAGP N RGD:5509061 20161208 MGI PMID:25048459 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0020400 cystinuria IAGP N RGD:5509061 20181025 MGI PMID:19484501 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0020400 cystinuria IAGP N RGD:5509061 20181025 MGI PMID:28165480 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0020401 argininuria IAGP N RGD:5509061 20161208 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0020401 argininuria IAGP N RGD:5509061 20161208 MGI PMID:25048459 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0020402 ornithinuria IAGP N RGD:5509061 20161208 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0020402 ornithinuria IAGP N RGD:5509061 20161208 MGI PMID:25048459 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0020403 lysinuria IAGP N RGD:5509061 20161208 MGI PMID:12923163 736530 Slc3a1 solute carrier family 3, member 1 gene MP:0020403 lysinuria IAGP N RGD:5509061 20161208 MGI PMID:25048459 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20220811 MGI 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15781580 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0001601 abnormal myelopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15781580 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15781580 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12058254 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:7650477 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8757814 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12058254 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15781580 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16717117 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16861683 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:7650477 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16861683 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:15781580 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15781580 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0008664 decreased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:15781580 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20150702 MGI PMID:16717117 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16717117 736533 Slc11a1 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 gene MP:0020186 abnormal susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:12058254 736542 Dpm2 dolichyl-phosphate mannosyltransferase subunit 2, regulatory gene MP:0000274 enlarged heart IEA N RGD:5509061 20160811 MGI 736542 Dpm2 dolichyl-phosphate mannosyltransferase subunit 2, regulatory gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20160421 MGI 736542 Dpm2 dolichyl-phosphate mannosyltransferase subunit 2, regulatory gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20211021 MGI 736542 Dpm2 dolichyl-phosphate mannosyltransferase subunit 2, regulatory gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:1996978 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0000603 pale liver IEA N RGD:5509061 20111116 MGI 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:3352223 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10100867 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:8325377 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:9140816 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9140816 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:1996978 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9140816 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:1996978 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:10100867 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0002661 abnormal corpus epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:10100867 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0003311 aminoaciduria IAGP N RGD:5509061 20141003 MGI PMID:8155735 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0003978 decreased circulating carnitine level IAGP N RGD:5509061 20141003 MGI PMID:8155735 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0004928 increased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:10100867 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0005309 increased circulating ammonia level IAGP N RGD:5509061 20141003 MGI PMID:1996978 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:8155735 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736544 Slc22a5 solute carrier family 22 (organic cation transporter), member 5 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 736547 Mxi1 MAX interactor 1, dimerization protein gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9624006 736547 Mxi1 MAX interactor 1, dimerization protein gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9624006 736547 Mxi1 MAX interactor 1, dimerization protein gene MP:0001167 prostate gland epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9624006 736547 Mxi1 MAX interactor 1, dimerization protein gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:9624006 736547 Mxi1 MAX interactor 1, dimerization protein gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9624006 736547 Mxi1 MAX interactor 1, dimerization protein gene MP:0002619 abnormal lymphocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9624006 736547 Mxi1 MAX interactor 1, dimerization protein gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:9624006 736547 Mxi1 MAX interactor 1, dimerization protein gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:9624006 736547 Mxi1 MAX interactor 1, dimerization protein gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9624006 736547 Mxi1 MAX interactor 1, dimerization protein gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9624006 736547 Mxi1 MAX interactor 1, dimerization protein gene MP:0008478 increased spleen white pulp amount IAGP N RGD:5509061 20141003 MGI PMID:9624006 736547 Mxi1 MAX interactor 1, dimerization protein gene MP:0009641 kidney degeneration IAGP N RGD:5509061 20141003 MGI PMID:9624006 736547 Mxi1 MAX interactor 1, dimerization protein gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20141003 MGI PMID:9624006 736547 Mxi1 MAX interactor 1, dimerization protein gene MP:0011423 kidney cortex atrophy IAGP N RGD:5509061 20141003 MGI PMID:9624006 736547 Mxi1 MAX interactor 1, dimerization protein gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:9624006 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9753165 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:17607354 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:17607354 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18832146 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18832146 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0001499 abnormal kindling response IAGP N RGD:5509061 20141003 MGI PMID:10529447 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:9753165 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:10529447 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220519 MGI 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:18832146 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:10529447 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15363892 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0002944 increased lactate dehydrogenase level IAGP N RGD:5509061 20141003 MGI PMID:17607354 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20230720 MGI PMID:25183173 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:9753165 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0003733 abnormal retina inner nuclear layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17607354 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15862894 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0004494 abnormal synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:11102482 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0004597 increased susceptibility to noise-induced hearing loss IAGP N RGD:5509061 20141003 MGI PMID:11102482 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0004611 increased susceptibility to ototoxicity-induced hearing loss IAGP N RGD:5509061 20141003 MGI PMID:15862894 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20230720 MGI PMID:25183173 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20230720 MGI PMID:25183173 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17607354 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0005403 abnormal nerve conduction IAGP N RGD:5509061 20141003 MGI PMID:15363892 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0005497 optic nerve cupping IAGP N RGD:5509061 20141003 MGI PMID:17607354 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0006219 optic nerve degeneration IAGP N RGD:5509061 20141003 MGI PMID:17607354 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20141003 MGI PMID:17607354 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18832146 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0008406 increased cellular sensitivity to hydrogen peroxide IAGP N RGD:5509061 20141003 MGI PMID:17607354 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0008946 abnormal neuron number IAGP N RGD:5509061 20230720 MGI PMID:25183173 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20230720 MGI PMID:25183173 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20230720 MGI PMID:25183173 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:18832146 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0010277 increased astrocytoma incidence IAGP N RGD:5509061 20160922 MGI PMID:26704996 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0010278 increased glioma incidence IAGP N RGD:5509061 20160922 MGI PMID:26704996 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0010312 increased oligodendroglioma incidence IAGP N RGD:5509061 20160922 MGI PMID:26704996 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0011272 short excitatory postsynaptic current rise time IAGP N RGD:5509061 20240418 MGI PMID:15363892 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0011273 prolonged excitatory postsynaptic current decay time IAGP N RGD:5509061 20240418 MGI PMID:15363892 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20220519 MGI 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:11102482 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11102482 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0012029 abnormal electroretinogram waveform feature IAGP N RGD:5509061 20141003 MGI PMID:17607354 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0012203 abnormal neuronal stem cell morphology IAGP N RGD:5509061 20230720 MGI PMID:25183173 736549 Slc1a3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 gene MP:0012206 increased neuronal stem cell self-renewal IAGP N RGD:5509061 20230720 MGI PMID:25183173 736551 Ppp2r2a protein phosphatase 2, regulatory subunit B, alpha gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20201022 MGI 736551 Ppp2r2a protein phosphatase 2, regulatory subunit B, alpha gene MP:0001258 decreased body length IEA N RGD:5509061 20181227 MGI 736551 Ppp2r2a protein phosphatase 2, regulatory subunit B, alpha gene MP:0001426 polydipsia IAGP N RGD:5509061 20180628 MGI PMID:26868295 736551 Ppp2r2a protein phosphatase 2, regulatory subunit B, alpha gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20180628 MGI PMID:26868295 736551 Ppp2r2a protein phosphatase 2, regulatory subunit B, alpha gene MP:0001759 increased urine glucose level IAGP N RGD:5509061 20180628 MGI PMID:26868295 736551 Ppp2r2a protein phosphatase 2, regulatory subunit B, alpha gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20180628 MGI PMID:26868295 736551 Ppp2r2a protein phosphatase 2, regulatory subunit B, alpha gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20181227 MGI 736551 Ppp2r2a protein phosphatase 2, regulatory subunit B, alpha gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 736551 Ppp2r2a protein phosphatase 2, regulatory subunit B, alpha gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20180628 MGI PMID:26868295 736551 Ppp2r2a protein phosphatase 2, regulatory subunit B, alpha gene MP:0005331 insulin resistance IAGP N RGD:5509061 20180628 MGI PMID:26868295 736551 Ppp2r2a protein phosphatase 2, regulatory subunit B, alpha gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20180628 MGI PMID:26868295 736551 Ppp2r2a protein phosphatase 2, regulatory subunit B, alpha gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20181227 MGI 736551 Ppp2r2a protein phosphatase 2, regulatory subunit B, alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:11717424 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:11717424 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:11717424 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:22031903 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:11717424 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:22031903 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11717424 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20150611 MGI PMID:25205113 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20200116 MGI PMID:31578378 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20150611 MGI PMID:25205113 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11717424 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20150611 MGI PMID:25205113 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:11717424 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20150611 MGI PMID:25205113 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:22031903 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0002061 abnormal aggression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:11717424 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11717424 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22031903 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:11717424 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:22031903 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:22031903 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:11717424 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22031903 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0003241 loss of cortex neurons IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0003246 loss of GABAergic neurons IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22031903 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141016 MGI PMID:25205113 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20200116 MGI PMID:31578378 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:22031903 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0005424 jerky movement IAGP N RGD:5509061 20141003 MGI PMID:11717424 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20200116 MGI PMID:31578378 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0006075 abnormal retina cone bipolar cell morphology IAGP N RGD:5509061 20200116 MGI PMID:31578378 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0006187 retina deposits IAGP N RGD:5509061 20200116 MGI PMID:31578378 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:22031903 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20200116 MGI PMID:31578378 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0008446 decreased retina cone cell number IAGP N RGD:5509061 20200116 MGI PMID:31578378 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20200116 MGI PMID:31578378 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:31578378 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200116 MGI PMID:31578378 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:22031903 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20141016 MGI PMID:25205113 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0008918 microgliosis IAGP N RGD:5509061 20200116 MGI PMID:31578378 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0009392 retina gliosis IAGP N RGD:5509061 20200116 MGI PMID:31578378 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0010762 abnormal microglial cell activation IAGP N RGD:5509061 20141016 MGI PMID:25205113 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200116 MGI PMID:31578378 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0012506 brain atrophy IAGP N RGD:5509061 20141003 MGI PMID:15649713 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0012506 brain atrophy IAGP N RGD:5509061 20141003 MGI PMID:22031903 736553 Ppt1 palmitoyl-protein thioesterase 1 gene MP:0030278 thick neurocranium IAGP N RGD:5509061 20171102 MGI PMID:11717424 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17314311 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18586888 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11708858 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:17314311 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18586888 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18586888 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:18586888 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:18586888 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18586888 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11708858 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0004079 abnormal putamen morphology IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:18586888 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18586888 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:17314311 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0005237 abnormal olfactory tract morphology IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0008026 abnormal brain white matter morphology IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0008547 abnormal neocortex morphology IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0008931 abnormal paraventricular thalamic nucleus morphology IAGP N RGD:5509061 20180315 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0009976 abnormal cerebellar peduncle morphology IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0009979 abnormal cerebellum deep nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11708858 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15569252 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0012736 abnormal polar body morphology IAGP N RGD:5509061 20141003 MGI PMID:17314311 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0014447 impaired spindle assembly in female meiosis IAGP N RGD:5509061 20240509 MGI PMID:17314311 736557 Pdha1 pyruvate dehydrogenase E1 alpha 1 gene MP:0020554 decreased stria medullaris size IAGP N RGD:5509061 20180315 MGI PMID:15569252 736561 F2rl2 coagulation factor II thrombin receptor like 2 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:9716134 736561 F2rl2 coagulation factor II thrombin receptor like 2 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:12384423 736561 F2rl2 coagulation factor II thrombin receptor like 2 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:12384423 736563 Lipa lysosomal acid lipase A gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9700186 736563 Lipa lysosomal acid lipase A gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:9700186 736563 Lipa lysosomal acid lipase A gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:9700186 736563 Lipa lysosomal acid lipase A gene MP:0000599 enlarged liver IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0000603 pale liver IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9700186 736563 Lipa lysosomal acid lipase A gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:9700186 736563 Lipa lysosomal acid lipase A gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9700186 736563 Lipa lysosomal acid lipase A gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9700186 736563 Lipa lysosomal acid lipase A gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:14644759 736563 Lipa lysosomal acid lipase A gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:14644759 736563 Lipa lysosomal acid lipase A gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:14644759 736563 Lipa lysosomal acid lipase A gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:14644759 736563 Lipa lysosomal acid lipase A gene MP:0002499 chronic inflammation IAGP N RGD:5509061 20141003 MGI PMID:14644759 736563 Lipa lysosomal acid lipase A gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:9700186 736563 Lipa lysosomal acid lipase A gene MP:0002981 increased liver weight IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0003333 liver fibrosis IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0004002 abnormal jejunum morphology IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:9700186 736563 Lipa lysosomal acid lipase A gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0005283 increased unsaturated fatty acids level IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0005285 decreased unsaturated fatty acids level IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0005336 abnormal inguinal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0005337 abnormal retroperitoneal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0005490 increased club cell number IAGP N RGD:5509061 20141003 MGI PMID:14644759 736563 Lipa lysosomal acid lipase A gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0006320 abnormal interscapular fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0008114 abnormal Kupffer cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0008245 abnormal alveolar macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:14644759 736563 Lipa lysosomal acid lipase A gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0008989 abnormal liver sinusoid morphology IAGP N RGD:5509061 20141003 MGI PMID:9700186 736563 Lipa lysosomal acid lipase A gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0009132 abnormal white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:9700186 736563 Lipa lysosomal acid lipase A gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:9700186 736563 Lipa lysosomal acid lipase A gene MP:0010027 increased liver cholesterol level IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:14644759 736563 Lipa lysosomal acid lipase A gene MP:0010951 abnormal lipid oxidation IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0010958 abnormal tricarboxylic acid cycle IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0011582 decreased triglyceride lipase activity IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:11290820 736563 Lipa lysosomal acid lipase A gene MP:0013243 abnormal carbohydrate metabolism IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0030973 impaired gluconeogenesis IAGP N RGD:5509061 20200409 MGI PMID:30639734 736563 Lipa lysosomal acid lipase A gene MP:0031058 hepatosplenomegaly IAGP N RGD:5509061 20200618 MGI PMID:11290820 736567 Vps52 VPS52 GARP complex subunit gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:23142660 736567 Vps52 VPS52 GARP complex subunit gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:23142660 736567 Vps52 VPS52 GARP complex subunit gene MP:0001723 disorganized yolk sac vascular plexus IAGP N RGD:5509061 20141003 MGI PMID:23142660 736567 Vps52 VPS52 GARP complex subunit gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:23142660 736567 Vps52 VPS52 GARP complex subunit gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23142660 736567 Vps52 VPS52 GARP complex subunit gene MP:0003171 phenotypic reversion IAGP N RGD:5509061 20141003 MGI PMID:23142660 736567 Vps52 VPS52 GARP complex subunit gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23142660 736567 Vps52 VPS52 GARP complex subunit gene MP:0004957 abnormal blastocyst morphology IAGP N RGD:5509061 20141003 MGI PMID:23142660 736567 Vps52 VPS52 GARP complex subunit gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:23142660 736567 Vps52 VPS52 GARP complex subunit gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23142660 736572 Psme2 proteasome (prosome, macropain) activator subunit 2 (PA28 beta) gene MP:0001837 defective assembly of class I molecules IAGP N RGD:5509061 20141003 MGI PMID:10591649 736572 Psme2 proteasome (prosome, macropain) activator subunit 2 (PA28 beta) gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:16569681 736572 Psme2 proteasome (prosome, macropain) activator subunit 2 (PA28 beta) gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10591649 736572 Psme2 proteasome (prosome, macropain) activator subunit 2 (PA28 beta) gene MP:0005079 decreased cytotoxic T cell cytolysis IAGP N RGD:5509061 20141003 MGI PMID:10591649 736577 Dmp1 dentin matrix protein 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18257058 736577 Dmp1 dentin matrix protein 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20151119 MGI PMID:21542006 736577 Dmp1 dentin matrix protein 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20210930 MGI PMID:33905568 736577 Dmp1 dentin matrix protein 1 gene MP:0000128 growth retardation of molars IAGP N RGD:5509061 20141003 MGI PMID:14966118 736577 Dmp1 dentin matrix protein 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:18257058 736577 Dmp1 dentin matrix protein 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20151119 MGI PMID:21542006 736577 Dmp1 dentin matrix protein 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:14514755 736577 Dmp1 dentin matrix protein 1 gene MP:0000168 abnormal bone marrow development IAGP N RGD:5509061 20151119 MGI PMID:21542006 736577 Dmp1 dentin matrix protein 1 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20151119 MGI PMID:17033621 736577 Dmp1 dentin matrix protein 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20151119 MGI PMID:17033621 736577 Dmp1 dentin matrix protein 1 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20151119 MGI PMID:21542006 736577 Dmp1 dentin matrix protein 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20151119 MGI PMID:21542006 736577 Dmp1 dentin matrix protein 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 736577 Dmp1 dentin matrix protein 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20151119 MGI PMID:17033621 736577 Dmp1 dentin matrix protein 1 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 736577 Dmp1 dentin matrix protein 1 gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20151119 MGI PMID:17033621 736577 Dmp1 dentin matrix protein 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0002577 reduced enamel thickness IAGP N RGD:5509061 20180215 MGI PMID:14966118 736577 Dmp1 dentin matrix protein 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20210930 MGI PMID:33905568 736577 Dmp1 dentin matrix protein 1 gene MP:0002817 abnormal tooth mineralization IAGP N RGD:5509061 20141003 MGI PMID:14966118 736577 Dmp1 dentin matrix protein 1 gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20141003 MGI PMID:14966118 736577 Dmp1 dentin matrix protein 1 gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0002819 abnormal dental pulp cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:14966118 736577 Dmp1 dentin matrix protein 1 gene MP:0002904 increased circulating parathyroid hormone level IAGP N RGD:5509061 20151119 MGI PMID:17033621 736577 Dmp1 dentin matrix protein 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20231207 MGI 736577 Dmp1 dentin matrix protein 1 gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20151119 MGI PMID:21542006 736577 Dmp1 dentin matrix protein 1 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20181227 MGI 736577 Dmp1 dentin matrix protein 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:18257058 736577 Dmp1 dentin matrix protein 1 gene MP:0003116 rickets IAGP N RGD:5509061 20151119 MGI PMID:17033621 736577 Dmp1 dentin matrix protein 1 gene MP:0003668 abnormal periodontal ligament morphology IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20231207 MGI 736577 Dmp1 dentin matrix protein 1 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18257058 736577 Dmp1 dentin matrix protein 1 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20151119 MGI PMID:21542006 736577 Dmp1 dentin matrix protein 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20231207 MGI 736577 Dmp1 dentin matrix protein 1 gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20141003 MGI PMID:14966118 736577 Dmp1 dentin matrix protein 1 gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20151119 MGI PMID:21542006 736577 Dmp1 dentin matrix protein 1 gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0005333 decreased heart rate IEA N RGD:5509061 20211021 MGI 736577 Dmp1 dentin matrix protein 1 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20151119 MGI PMID:17033621 736577 Dmp1 dentin matrix protein 1 gene MP:0005566 decreased blood urea nitrogen level IEA N RGD:5509061 20231207 MGI 736577 Dmp1 dentin matrix protein 1 gene MP:0006400 decreased molar number IAGP N RGD:5509061 20180215 MGI PMID:14966118 736577 Dmp1 dentin matrix protein 1 gene MP:0008151 increased diameter of long bones IAGP N RGD:5509061 20141003 MGI PMID:14514755 736577 Dmp1 dentin matrix protein 1 gene MP:0008753 abnormal osteocyte morphology IAGP N RGD:5509061 20180215 MGI PMID:17033621 736577 Dmp1 dentin matrix protein 1 gene MP:0009445 osteomalacia IAGP N RGD:5509061 20151119 MGI PMID:17033621 736577 Dmp1 dentin matrix protein 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20231207 MGI 736577 Dmp1 dentin matrix protein 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 736577 Dmp1 dentin matrix protein 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20231207 MGI 736577 Dmp1 dentin matrix protein 1 gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20211021 MGI 736577 Dmp1 dentin matrix protein 1 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20151119 MGI PMID:21542006 736577 Dmp1 dentin matrix protein 1 gene MP:0010926 increased osteoid volume IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0011584 increased alkaline phosphatase activity IAGP N RGD:5509061 20151119 MGI PMID:21542006 736577 Dmp1 dentin matrix protein 1 gene MP:0011712 arrested osteoblast differentiation IAGP N RGD:5509061 20171221 MGI PMID:21542006 736577 Dmp1 dentin matrix protein 1 gene MP:0011721 abnormal bone mineralization involved in bone maturation IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030131 abnormal periodontium morphology IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030451 abnormal dentin mineralization IAGP N RGD:5509061 20180215 MGI PMID:14966118 736577 Dmp1 dentin matrix protein 1 gene MP:0030452 abnormal cementum mineralization IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030466 alveolar process atrophy IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030484 abnormal osteocyte lacuna morphology IAGP N RGD:5509061 20180215 MGI PMID:17033621 736577 Dmp1 dentin matrix protein 1 gene MP:0030484 abnormal osteocyte lacuna morphology IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030485 abnormal osteocyte lacunocanalicular system morphology IAGP N RGD:5509061 20180215 MGI PMID:17033621 736577 Dmp1 dentin matrix protein 1 gene MP:0030485 abnormal osteocyte lacunocanalicular system morphology IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030486 abnormal osteocyte canaliculus morphology IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030540 misaligned teeth IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030542 abnormal dentin development IAGP N RGD:5509061 20180215 MGI PMID:14966118 736577 Dmp1 dentin matrix protein 1 gene MP:0030543 abnormal predentin morphology IAGP N RGD:5509061 20180215 MGI PMID:14966118 736577 Dmp1 dentin matrix protein 1 gene MP:0030545 abnormal acellular cementum morphology IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030546 abnormal cellular cementum morphology IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030549 abnormal cementocyte lacunocanalicular system morphology IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030550 abnormal cementoblast morphology IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030552 decreased cementoblast number IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030555 abnormal cementocyte lacuna morphology IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030556 abnormal cementocyte canaliculus morphology IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030557 abnormal cementocyte dendritic process morphology IAGP N RGD:5509061 20180215 MGI PMID:18573980 736577 Dmp1 dentin matrix protein 1 gene MP:0030884 rachitic rosary IAGP N RGD:5509061 20181101 MGI PMID:17033621 736580 Gdf9 growth differentiation factor 9 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11376106 736580 Gdf9 growth differentiation factor 9 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:11376106 736580 Gdf9 growth differentiation factor 9 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:8849725 736580 Gdf9 growth differentiation factor 9 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:8849725 736580 Gdf9 growth differentiation factor 9 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:11376106 736580 Gdf9 growth differentiation factor 9 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:8849725 736580 Gdf9 growth differentiation factor 9 gene MP:0001132 absent mature ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:8849725 736580 Gdf9 growth differentiation factor 9 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11376106 736580 Gdf9 growth differentiation factor 9 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:8849725 736580 Gdf9 growth differentiation factor 9 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:8849725 736580 Gdf9 growth differentiation factor 9 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:8849725 736580 Gdf9 growth differentiation factor 9 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:11376106 736580 Gdf9 growth differentiation factor 9 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11376106 736580 Gdf9 growth differentiation factor 9 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8849725 736580 Gdf9 growth differentiation factor 9 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:8849725 736580 Gdf9 growth differentiation factor 9 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11376106 736580 Gdf9 growth differentiation factor 9 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:11376106 736580 Gdf9 growth differentiation factor 9 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:8849725 736580 Gdf9 growth differentiation factor 9 gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:11376106 736580 Gdf9 growth differentiation factor 9 gene MP:0003696 abnormal zona pellucida morphology IAGP N RGD:5509061 20141003 MGI PMID:11376106 736580 Gdf9 growth differentiation factor 9 gene MP:0004805 absent oocytes IAGP N RGD:5509061 20141003 MGI PMID:11376106 736580 Gdf9 growth differentiation factor 9 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:11376106 736580 Gdf9 growth differentiation factor 9 gene MP:0009374 absent cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:11376106 736580 Gdf9 growth differentiation factor 9 gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20141003 MGI PMID:11376106 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17013884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15226444 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17013884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20622884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15226444 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:20622884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:20622884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0000704 abnormal thymus development IAGP N RGD:5509061 20141003 MGI PMID:20622884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:15226444 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17013884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0001648 abnormal apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15226444 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15226444 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:17013884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15226444 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20622884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:20622884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20622884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17013884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:17013884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0003403 absent placental labyrinth IAGP N RGD:5509061 20141003 MGI PMID:17013884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:20622884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17013884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0004229 abnormal embryonic erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:17013884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0004255 abnormal spongiotrophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15226444 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:17013884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17013884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:15226444 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:17013884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17013884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15226444 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0011204 abnormal visceral yolk sac blood island morphology IAGP N RGD:5509061 20141003 MGI PMID:17013884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17013884 736581 Zfp36l1 zinc finger protein 36, C3H type-like 1 gene MP:0031590 abnormal epicardium development IAGP N RGD:5509061 20240229 MGI PMID:15226444 736583 Rab3b RAB3B, member RAS oncogene family gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15269275 736583 Rab3b RAB3B, member RAS oncogene family gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15269275 736583 Rab3b RAB3B, member RAS oncogene family gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:15269275 736583 Rab3b RAB3B, member RAS oncogene family gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15269275 736583 Rab3b RAB3B, member RAS oncogene family gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15269275 736583 Rab3b RAB3B, member RAS oncogene family gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15269275 736583 Rab3b RAB3B, member RAS oncogene family gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:16436611 736583 Rab3b RAB3B, member RAS oncogene family gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15269275 736583 Rab3b RAB3B, member RAS oncogene family gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16436611 736583 Rab3b RAB3B, member RAS oncogene family gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:16436611 736583 Rab3b RAB3B, member RAS oncogene family gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:15269275 736583 Rab3b RAB3B, member RAS oncogene family gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:15269275 736583 Rab3b RAB3B, member RAS oncogene family gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15269275 736583 Rab3b RAB3B, member RAS oncogene family gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15269275 736584 Hapln2 hyaluronan and proteoglycan link protein 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:20181608 736584 Hapln2 hyaluronan and proteoglycan link protein 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:20181608 736584 Hapln2 hyaluronan and proteoglycan link protein 2 gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20141003 MGI PMID:20181608 736586 Adcy8 adenylate cyclase 8 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10864938 736586 Adcy8 adenylate cyclase 8 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10864938 736586 Adcy8 adenylate cyclase 8 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:10482244 736586 Adcy8 adenylate cyclase 8 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10482244 736586 Adcy8 adenylate cyclase 8 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:10864938 736586 Adcy8 adenylate cyclase 8 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:20837544 736586 Adcy8 adenylate cyclase 8 gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:10864938 736586 Adcy8 adenylate cyclase 8 gene MP:0004000 impaired passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:10482244 736586 Adcy8 adenylate cyclase 8 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:12441059 736586 Adcy8 adenylate cyclase 8 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:10864938 736586 Adcy8 adenylate cyclase 8 gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:12441059 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17960025 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17960025 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20230601 MGI PMID:17738154 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000381 enlarged hair follicles IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000384 distorted hair follicle pattern IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16040962 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000414 alopecia IAGP N RGD:5509061 20230601 MGI PMID:17738154 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000416 sparse hair IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000417 short hair IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000649 sebaceous gland atrophy IAGP N RGD:5509061 20141003 MGI PMID:11533264 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0000649 sebaceous gland atrophy IAGP N RGD:5509061 20141003 MGI PMID:16040962 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001192 scaly skin IAGP N RGD:5509061 20141003 MGI PMID:16040962 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:16040962 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:16040962 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20230601 MGI PMID:17738154 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:631559 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001345 Meibomian gland atrophy IAGP N RGD:5509061 20141003 MGI PMID:11533264 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001433 polyphagia IAGP N RGD:5509061 20141003 MGI PMID:12177411 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:17960025 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20230601 MGI PMID:17738154 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12177411 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20230601 MGI PMID:17738154 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20230601 MGI PMID:17738154 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20230601 MGI PMID:17738154 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002001 blindness IAGP N RGD:5509061 20230601 MGI PMID:17738154 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:631559 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20230601 MGI PMID:17738154 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002073 abnormal hair growth IAGP N RGD:5509061 20230601 MGI PMID:17738154 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16040962 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002500 granulomatous inflammation IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:12177411 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:17960025 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12177411 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20220630 MGI PMID:21856199 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0002992 abnormal sebaceous lipid secretion IAGP N RGD:5509061 20141003 MGI PMID:16040962 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0003413 hair follicle degeneration IEA N RGD:5509061 20220707 MGI 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20230601 MGI PMID:17738154 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0003846 matted coat IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0003853 dry skin IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17960025 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17960025 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20220630 MGI PMID:17960025 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005266 abnormal metabolism IEA N RGD:5509061 20160428 MGI 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11533264 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005284 increased saturated fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:11533264 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005285 decreased unsaturated fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:11533264 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:11533264 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:12177411 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12177411 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17960025 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005334 abnormal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:17960025 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:18719666 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:5924301 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0006319 abnormal epididymal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17960025 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0008418 abnormal cutaneous elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:631559 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:631559 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17960025 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0008900 abnormal uterine fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:17960025 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0009004 progressive hair loss IAGP N RGD:5509061 20141003 MGI PMID:11533264 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0009011 prolonged diestrus IAGP N RGD:5509061 20230601 MGI PMID:17738154 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0009293 decreased inguinal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0009305 decreased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17960025 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20220630 MGI PMID:21856199 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0009535 abnormal skin sebaceous gland morphology IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0009545 abnormal dermis papillary layer morphology IEA N RGD:5509061 20220714 MGI 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0009675 orthokeratosis IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:18054317 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0010681 abnormal hair follicle bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0010684 abnormal hair follicle outer root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0010685 abnormal hair follicle inner root sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0010686 abnormal hair follicle matrix region morphology IEA N RGD:5509061 20220714 MGI 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:17960025 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0012725 small sebaceous gland IAGP N RGD:5509061 20141218 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0013193 sebaceous gland hypoplasia IAGP N RGD:5509061 20141218 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0013193 sebaceous gland hypoplasia IAGP N RGD:5509061 20141218 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0013375 abnormal sebocyte morphology IAGP N RGD:5509061 20141218 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0013375 abnormal sebocyte morphology IAGP N RGD:5509061 20141218 MGI PMID:15278437 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0013382 small perianal sebaceous gland IAGP N RGD:5509061 20141218 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0013388 small Meibomian gland IAGP N RGD:5509061 20141225 MGI PMID:10854228 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0013787 photophobia IEA N RGD:5509061 20150611 MGI 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0030570 abnormal piliary canal morphology IEA N RGD:5509061 20180524 MGI 736587 Scd1 stearoyl-Coenzyme A desaturase 1 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:18054317 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0000160 kyphosis IEA N RGD:5509061 20141003 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0000192 abnormal mineral level IAGP N RGD:5509061 20161124 MGI PMID:26660102 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0000198 decreased circulating phosphate level IAGP N RGD:5509061 20161124 MGI PMID:26660102 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0000297 abnormal atrioventricular cushion morphology IEA N RGD:5509061 20170504 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20161124 MGI PMID:23934451 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20161124 MGI PMID:23934451 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20170504 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20210128 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20141003 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0001304 cataract IEA N RGD:5509061 20141003 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0001319 irregularly shaped pupil IEA N RGD:5509061 20201231 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20150108 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20201022 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20181227 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0002947 increased hemangioma incidence IEA N RGD:5509061 20210930 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0003869 ectopic cartilage IEA N RGD:5509061 20170504 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20141003 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0005176 eyelids fail to open IEA N RGD:5509061 20160114 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0005287 narrow eye opening IEA N RGD:5509061 20201231 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20160421 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0006007 abnormal basal ganglion morphology IAGP N RGD:5509061 20161124 MGI PMID:23934451 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0006062 abnormal vena cava morphology IEA N RGD:5509061 20170504 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0006093 arteriovenous malformation IEA N RGD:5509061 20170504 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0006358 absent pinna reflex IEA N RGD:5509061 20170105 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0008918 microgliosis IAGP N RGD:5509061 20161124 MGI PMID:23934451 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0009820 abnormal liver vasculature morphology IEA N RGD:5509061 20170504 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20150108 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20210128 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0010096 abnormal incisor color IEA N RGD:5509061 20170105 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20220811 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0010440 anomalous pulmonary venous connection IEA N RGD:5509061 20170504 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20240523 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20170504 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0013968 multiple persisting craniopharyngeal ducts IEA N RGD:5509061 20170504 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0014018 embryo tumor IEA N RGD:5509061 20170504 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0014019 embryo cyst IEA N RGD:5509061 20170504 MGI 736588 Slc20a2 solute carrier family 20, member 2 gene MP:0030014 calcified brain IAGP N RGD:5509061 20170713 MGI PMID:23934451 736590 Ptpn5 protein tyrosine phosphatase, non-receptor type 5 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 736591 Kcna3 potassium voltage-gated channel, shaker-related subfamily, member 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12588802 736591 Kcna3 potassium voltage-gated channel, shaker-related subfamily, member 3 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14981264 736591 Kcna3 potassium voltage-gated channel, shaker-related subfamily, member 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12878608 736591 Kcna3 potassium voltage-gated channel, shaker-related subfamily, member 3 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14981264 736591 Kcna3 potassium voltage-gated channel, shaker-related subfamily, member 3 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:14981264 736591 Kcna3 potassium voltage-gated channel, shaker-related subfamily, member 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:12588802 736591 Kcna3 potassium voltage-gated channel, shaker-related subfamily, member 3 gene MP:0008965 increased basal metabolism IAGP N RGD:5509061 20141003 MGI PMID:12588802 736591 Kcna3 potassium voltage-gated channel, shaker-related subfamily, member 3 gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:14981264 736596 Sparcl1 SPARC-like 1 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20018883 736596 Sparcl1 SPARC-like 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 736596 Sparcl1 SPARC-like 1 gene MP:0002183 gliosis IAGP N RGD:5509061 20141003 MGI PMID:20018883 736596 Sparcl1 SPARC-like 1 gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 736599 Egr3 early growth response 3 gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:9731539 736599 Egr3 early growth response 3 gene MP:0000161 scoliosis IAGP N RGD:5509061 20220616 MGI PMID:28829946 736599 Egr3 early growth response 3 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:9731539 736599 Egr3 early growth response 3 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19954518 736599 Egr3 early growth response 3 gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:19954518 736599 Egr3 early growth response 3 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:19954518 736599 Egr3 early growth response 3 gene MP:0000959 abnormal somatic sensory system morphology IAGP N RGD:5509061 20141003 MGI PMID:9731539 736599 Egr3 early growth response 3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:9731539 736599 Egr3 early growth response 3 gene MP:0001025 abnormal sympathetic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:23467373 736599 Egr3 early growth response 3 gene MP:0001038 abnormal cholinergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:19954518 736599 Egr3 early growth response 3 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:23467373 736599 Egr3 early growth response 3 gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:9731539 736599 Egr3 early growth response 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:19369542 736599 Egr3 early growth response 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:9731539 736599 Egr3 early growth response 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:19369542 736599 Egr3 early growth response 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:9731539 736599 Egr3 early growth response 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20220616 MGI PMID:28829946 736599 Egr3 early growth response 3 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:19369542 736599 Egr3 early growth response 3 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:19369542 736599 Egr3 early growth response 3 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:11978828 736599 Egr3 early growth response 3 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:11978828 736599 Egr3 early growth response 3 gene MP:0004069 abnormal muscle spindle morphology IAGP N RGD:5509061 20141003 MGI PMID:11978828 736599 Egr3 early growth response 3 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:9731539 736599 Egr3 early growth response 3 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11978828 736599 Egr3 early growth response 3 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9731539 736599 Egr3 early growth response 3 gene MP:0005423 abnormal somatic nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:11978828 736599 Egr3 early growth response 3 gene MP:0008468 absent muscle spindles IAGP N RGD:5509061 20141003 MGI PMID:9731539 736599 Egr3 early growth response 3 gene MP:0008838 decreased transforming growth factor beta level IAGP N RGD:5509061 20141003 MGI PMID:23904169 736599 Egr3 early growth response 3 gene MP:0009284 abnormal sympathetic neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:23467373 736599 Egr3 early growth response 3 gene MP:0009561 superior cervical ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:23467373 736599 Egr3 early growth response 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9731539 736602 Scn3a sodium channel, voltage-gated, type III, alpha gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 736602 Scn3a sodium channel, voltage-gated, type III, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17052333 736602 Scn3a sodium channel, voltage-gated, type III, alpha gene MP:0005202 lethargy IEA N RGD:5509061 20111116 MGI 736602 Scn3a sodium channel, voltage-gated, type III, alpha gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20111116 MGI 736602 Scn3a sodium channel, voltage-gated, type III, alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 736604 Rps20 ribosomal protein S20 gene MP:0000575 increased foot pad pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 736604 Rps20 ribosomal protein S20 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 736604 Rps20 ribosomal protein S20 gene MP:0002095 abnormal skin pigmentation IEA N RGD:5509061 20111116 MGI 736604 Rps20 ribosomal protein S20 gene MP:0009387 abnormal epidermal pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 736604 Rps20 ribosomal protein S20 gene MP:0009388 abnormal epidermal melanocyte morphology IAGP N RGD:5509061 20181227 MGI PMID:18641651 736604 Rps20 ribosomal protein S20 gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20181227 MGI PMID:18641651 736604 Rps20 ribosomal protein S20 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12533510 736604 Rps20 ribosomal protein S20 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20181227 MGI PMID:18641651 736604 Rps20 ribosomal protein S20 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736604 Rps20 ribosomal protein S20 gene MP:0011276 increased tail pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 736604 Rps20 ribosomal protein S20 gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20181227 MGI PMID:18641651 736604 Rps20 ribosomal protein S20 gene MP:0012022 increased melanocyte number IAGP N RGD:5509061 20181227 MGI PMID:18641651 736604 Rps20 ribosomal protein S20 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0000282 abnormal interatrial septum morphology IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20180719 MGI PMID:22493258 736609 Polb polymerase (DNA directed), beta gene MP:0000640 adrenal gland hypoplasia IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0000788 abnormal cerebral cortex morphology IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0001015 small superior cervical ganglion IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0001100 abnormal vagus ganglion morphology IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0001102 small superior vagus ganglion IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0001177 atelectasis IAGP N RGD:5509061 20180719 MGI PMID:10716939 736609 Polb polymerase (DNA directed), beta gene MP:0001194 dermatitis IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0001247 dermal cyst IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20180719 MGI PMID:22493258 736609 Polb polymerase (DNA directed), beta gene MP:0001575 cyanosis IAGP N RGD:5509061 20180719 MGI PMID:10716939 736609 Polb polymerase (DNA directed), beta gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0001953 respiratory failure IAGP N RGD:5509061 20180719 MGI PMID:10716939 736609 Polb polymerase (DNA directed), beta gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20180719 MGI PMID:10716939 736609 Polb polymerase (DNA directed), beta gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20180719 MGI PMID:10716939 736609 Polb polymerase (DNA directed), beta gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0002493 increased IgG level IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20211021 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0002951 small thyroid gland IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0003048 abnormal cervical vertebrae morphology IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0003077 abnormal cell cycle IAGP N RGD:5509061 20180719 MGI PMID:22493258 736609 Polb polymerase (DNA directed), beta gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20180719 MGI PMID:10716939 736609 Polb polymerase (DNA directed), beta gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20180719 MGI PMID:22493258 736609 Polb polymerase (DNA directed), beta gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0003717 pallor IAGP N RGD:5509061 20180719 MGI PMID:10716939 736609 Polb polymerase (DNA directed), beta gene MP:0003865 lymph node inflammation IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20180719 MGI PMID:22493258 736609 Polb polymerase (DNA directed), beta gene MP:0003960 increased lean body mass IEA N RGD:5509061 20201022 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20180719 MGI PMID:10716939 736609 Polb polymerase (DNA directed), beta gene MP:0004252 abnormal direction of heart looping IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0004269 abnormal optic cup morphology IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0004607 abnormal cervical atlas morphology IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0004666 absent stapedial artery IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0004815 abnormal somatic hypermutation frequency IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20180719 MGI PMID:10716939 736609 Polb polymerase (DNA directed), beta gene MP:0006408 dorsal root ganglion hypoplasia IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0008090 increased T-helper 2 cell number IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0008128 abnormal brain internal capsule morphology IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0008481 increased spleen germinal center number IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0008491 dorsal root ganglion hyperplasia IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0008542 enlarged cervical lymph nodes IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0008760 abnormal immunoglobulin heavy chain V(D)J recombination IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20180719 MGI PMID:22493258 736609 Polb polymerase (DNA directed), beta gene MP:0008922 abnormal cervical rib IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0008943 increased sensitivity to induced cell death IAGP N RGD:5509061 20180719 MGI PMID:22493258 736609 Polb polymerase (DNA directed), beta gene MP:0009322 increased splenocyte apoptosis IAGP N RGD:5509061 20180719 MGI PMID:22493258 736609 Polb polymerase (DNA directed), beta gene MP:0009322 increased splenocyte apoptosis IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0009516 enlarged salivary gland IAGP N RGD:5509061 20180719 MGI PMID:24388753 736609 Polb polymerase (DNA directed), beta gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20180719 MGI PMID:22493258 736609 Polb polymerase (DNA directed), beta gene MP:0009796 abnormal base-excision repair IAGP N RGD:5509061 20180719 MGI PMID:22493258 736609 Polb polymerase (DNA directed), beta gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20180719 MGI PMID:10716939 736609 Polb polymerase (DNA directed), beta gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:10716939 736609 Polb polymerase (DNA directed), beta gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:22493258 736609 Polb polymerase (DNA directed), beta gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20180719 MGI PMID:8016642 736609 Polb polymerase (DNA directed), beta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20180719 MGI PMID:8016642 736609 Polb polymerase (DNA directed), beta gene MP:0011368 increased kidney apoptosis IAGP N RGD:5509061 20180719 MGI PMID:22493258 736609 Polb polymerase (DNA directed), beta gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20180719 MGI PMID:22493258 736609 Polb polymerase (DNA directed), beta gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20180719 MGI PMID:22493258 736609 Polb polymerase (DNA directed), beta gene MP:0013827 thin oculomotor nerve IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0013828 thin facial nerve IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0013829 thin splanchnic nerve IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0013836 abnormal hypoglossal nerve topology IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0013841 abnormal lymphatic vessel topology IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0013851 abnormal Wolffian duct topology IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0013875 increased trigeminal neuroma incidence IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0013928 thin motoric part of trigeminal nerve IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0013952 retroesophageal left subclavian artery IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0013969 reduced sympathetic cervical ganglion size IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0013982 inverse situs of great intrathoracic arteries IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0014002 absent extracranial vertebral artery segment IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0014017 abnormal Wolffian duct connection IEA N RGD:5509061 20180719 MGI 736609 Polb polymerase (DNA directed), beta gene MP:0020500 persistent trigeminal artery IEA N RGD:5509061 20180719 MGI 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:11032718 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11032718 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0001426 polydipsia IAGP N RGD:5509061 20141003 MGI PMID:10913167 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:10913167 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:11032718 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20410296 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0002986 decreased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:10913167 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:10913167 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:11032718 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0004860 dilated kidney collecting duct IAGP N RGD:5509061 20141003 MGI PMID:10913167 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:11032718 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:10913167 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0006317 decreased urine sodium level IAGP N RGD:5509061 20141003 MGI PMID:10913167 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0010092 increased circulating magnesium level IAGP N RGD:5509061 20141003 MGI PMID:11032718 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0010108 abnormal renal water reabsorption IAGP N RGD:5509061 20141003 MGI PMID:10913167 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0011229 abnormal vitamin C level IAGP N RGD:5509061 20141003 MGI PMID:20410296 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0011333 abnormal kidney inner medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:10913167 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0011460 decreased urine chloride ion level IAGP N RGD:5509061 20141003 MGI PMID:10913167 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0011467 decreased urine urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:10913167 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:10913167 736610 Akr1b1 aldo-keto reductase family 1 member B gene MP:0030884 rachitic rosary IAGP N RGD:5509061 20181101 MGI PMID:20410296 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:22048155 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:22048155 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22048155 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:22048155 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:22048155 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:22048155 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22048155 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:22048155 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22048155 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:22048155 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:22048155 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19449316 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22048155 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:19449316 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20141003 MGI PMID:19449316 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:22048155 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22048155 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:22048155 736611 Kidins220 kinase D-interacting substrate 220 gene MP:0030005 increased retina apoptosis IAGP N RGD:5509061 20170706 MGI PMID:22048155 736614 Zdhhc2 zinc finger, DHHC domain containing 2 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20210429 MGI PMID:33488612 736614 Zdhhc2 zinc finger, DHHC domain containing 2 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20210429 MGI PMID:33488612 736614 Zdhhc2 zinc finger, DHHC domain containing 2 gene MP:0002753 dilated heart left ventricle IEA N RGD:5509061 20211021 MGI 736614 Zdhhc2 zinc finger, DHHC domain containing 2 gene MP:0003769 abnormal lip morphology IEA N RGD:5509061 20190502 MGI 736614 Zdhhc2 zinc finger, DHHC domain containing 2 gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20210429 MGI PMID:33488612 736614 Zdhhc2 zinc finger, DHHC domain containing 2 gene MP:0008346 increased gamma-delta T cell number IAGP N RGD:5509061 20210429 MGI PMID:33488612 736614 Zdhhc2 zinc finger, DHHC domain containing 2 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20210429 MGI PMID:33488612 736614 Zdhhc2 zinc finger, DHHC domain containing 2 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20210429 MGI PMID:33488612 736614 Zdhhc2 zinc finger, DHHC domain containing 2 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20210429 MGI PMID:33488612 736614 Zdhhc2 zinc finger, DHHC domain containing 2 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20210429 MGI PMID:33488612 736614 Zdhhc2 zinc finger, DHHC domain containing 2 gene MP:0008769 abnormal plasmacytoid dendritic cell physiology IAGP N RGD:5509061 20210429 MGI PMID:33488612 736614 Zdhhc2 zinc finger, DHHC domain containing 2 gene MP:0012573 decreased susceptibility to chemically induced skin inflammation IAGP N RGD:5509061 20210429 MGI PMID:33488612 736614 Zdhhc2 zinc finger, DHHC domain containing 2 gene MP:0012764 increased alpha-beta T cell number IAGP N RGD:5509061 20210429 MGI PMID:33488612 736614 Zdhhc2 zinc finger, DHHC domain containing 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 736614 Zdhhc2 zinc finger, DHHC domain containing 2 gene MP:0013410 decreased dendritic epidermal T cell number IAGP N RGD:5509061 20210429 MGI PMID:33488612 736617 Niban1 niban apoptosis regulator 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210826 MGI 736617 Niban1 niban apoptosis regulator 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210826 MGI 736617 Niban1 niban apoptosis regulator 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210826 MGI 736617 Niban1 niban apoptosis regulator 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210826 MGI 736617 Niban1 niban apoptosis regulator 1 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210826 MGI 736617 Niban1 niban apoptosis regulator 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17588536 736617 Niban1 niban apoptosis regulator 1 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20210826 MGI 736617 Niban1 niban apoptosis regulator 1 gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20240523 MGI 736617 Niban1 niban apoptosis regulator 1 gene MP:0011496 abnormal head size IEA N RGD:5509061 20210826 MGI 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141106 MGI PMID:18276892 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141106 MGI PMID:18276892 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0000751 myopathy IAGP N RGD:5509061 20141106 MGI PMID:18276892 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141106 MGI PMID:16449238 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141106 MGI PMID:18276892 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141106 MGI PMID:16449238 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0001785 edema IAGP N RGD:5509061 20141106 MGI PMID:18276892 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141106 MGI PMID:18276892 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141106 MGI PMID:18276892 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141106 MGI PMID:16449238 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141106 MGI PMID:18276892 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141106 MGI PMID:18276892 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141106 MGI PMID:18276892 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141106 MGI PMID:18276892 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0008775 abnormal heart ventricle pressure IAGP N RGD:5509061 20141106 MGI PMID:18276892 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141106 MGI PMID:16449238 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0010956 abnormal mitochondrial ATP synthesis coupled electron transport IAGP N RGD:5509061 20141106 MGI PMID:18276892 736621 mt-Co1 cytochrome c oxidase I, mitochondrial gene MP:0013405 increased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:16449238 736626 Klre1 killer cell lectin-like receptor family E member 1 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:15069013 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000166 abnormal chondrocyte morphology IEA N RGD:5509061 20111116 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000432 abnormal head morphology IEA N RGD:5509061 20201022 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:17728275 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000440 domed cranium IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000443 abnormal snout morphology IEA N RGD:5509061 20201022 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000550 abnormal forelimb morphology IEA N RGD:5509061 20201022 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000556 abnormal hindlimb morphology IEA N RGD:5509061 20201022 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000588 thick tail IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:17728275 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000745 tremors IEA N RGD:5509061 20201022 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:24431432 736630 Npr2 natriuretic peptide receptor 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:19805384 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001056 abnormal cranial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:24431432 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:24431432 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:17728275 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24431432 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201022 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001406 abnormal gait IEA N RGD:5509061 20201022 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001512 trunk curl IEA N RGD:5509061 20201022 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:20616347 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001931 abnormal oogenesis IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0001935 decreased litter size IEA N RGD:5509061 20111116 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002089 abnormal postnatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20201022 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:624676 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:17728275 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:17728275 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:3840788 736630 Npr2 natriuretic peptide receptor 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:20616347 736630 Npr2 natriuretic peptide receptor 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004340 short scapula IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004386 enlarged interparietal bone IAGP N RGD:5509061 20141003 MGI PMID:17728275 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004421 enlarged parietal bone IAGP N RGD:5509061 20141003 MGI PMID:17728275 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004444 small supraoccipital bone IAGP N RGD:5509061 20141003 MGI PMID:17728275 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20141003 MGI PMID:17728275 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004595 abnormal mandibular condyloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:886262 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004673 splayed ribs IEA N RGD:5509061 20111116 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0004831 long incisors IAGP N RGD:5509061 20171005 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0005168 abnormal female meiosis IAGP N RGD:5509061 20141003 MGI PMID:20947764 736630 Npr2 natriuretic peptide receptor 2 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0006397 disorganized long bone epiphyseal plate IEA N RGD:5509061 20111116 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0008158 increased diameter of femur IEA N RGD:5509061 20111116 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0008257 thin myometrium IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0008258 thin endometrium IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17728275 736630 Npr2 natriuretic peptide receptor 2 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0008526 decreased cranium width IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0008736 micromelia IEA N RGD:5509061 20111116 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:23065701 736630 Npr2 natriuretic peptide receptor 2 gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0009088 thin uterine horn IAGP N RGD:5509061 20141003 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:20616347 736630 Npr2 natriuretic peptide receptor 2 gene MP:0009456 impaired cued conditioning behavior IEA N RGD:5509061 20230601 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0009677 abnormal spinal cord dorsal column morphology IAGP N RGD:5509061 20141003 MGI PMID:19805384 736630 Npr2 natriuretic peptide receptor 2 gene MP:0009854 impaired gastric peristalsis IAGP N RGD:5509061 20141003 MGI PMID:20616347 736630 Npr2 natriuretic peptide receptor 2 gene MP:0009861 abnormal pyloric sphincter morphology IAGP N RGD:5509061 20141003 MGI PMID:20616347 736630 Npr2 natriuretic peptide receptor 2 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:886262 736630 Npr2 natriuretic peptide receptor 2 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20141003 MGI PMID:20616347 736630 Npr2 natriuretic peptide receptor 2 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20616347 736630 Npr2 natriuretic peptide receptor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17728275 736630 Npr2 natriuretic peptide receptor 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0011496 abnormal head size IEA N RGD:5509061 20201022 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0011862 decreased cranium length IAGP N RGD:5509061 20170907 MGI PMID:5713631 736630 Npr2 natriuretic peptide receptor 2 gene MP:0011999 abnormal tail length IEA N RGD:5509061 20201022 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20230601 MGI 736630 Npr2 natriuretic peptide receptor 2 gene MP:0030082 long lower incisors IAGP N RGD:5509061 20171005 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0030083 long upper incisors IAGP N RGD:5509061 20171005 MGI PMID:15572448 736630 Npr2 natriuretic peptide receptor 2 gene MP:0030245 round head IEA N RGD:5509061 20171019 MGI 736640 Syngr1 synaptogyrin 1 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 736640 Syngr1 synaptogyrin 1 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 736640 Syngr1 synaptogyrin 1 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 736640 Syngr1 synaptogyrin 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 736640 Syngr1 synaptogyrin 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 736640 Syngr1 synaptogyrin 1 gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230601 MGI 736640 Syngr1 synaptogyrin 1 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 736640 Syngr1 synaptogyrin 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:10595519 736640 Syngr1 synaptogyrin 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:10595519 736640 Syngr1 synaptogyrin 1 gene MP:0002064 seizures IEA N RGD:5509061 20150219 MGI 736640 Syngr1 synaptogyrin 1 gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 736640 Syngr1 synaptogyrin 1 gene MP:0002764 short tibia IEA N RGD:5509061 20240523 MGI 736640 Syngr1 synaptogyrin 1 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:10595519 736640 Syngr1 synaptogyrin 1 gene MP:0002922 decreased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:10595519 736640 Syngr1 synaptogyrin 1 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20230601 MGI 736643 Sncg synuclein, gamma gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:15147505 736643 Sncg synuclein, gamma gene MP:0011452 decreased susceptibility to dopaminergic neuron neurotoxicity IAGP N RGD:5509061 20141003 MGI PMID:15147505 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0001184 absent pulmonary alveoli IAGP N RGD:5509061 20141003 MGI PMID:9716527 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0001257 increased body length IEA N RGD:5509061 20200402 MGI 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9716527 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9716527 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:20068154 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:9716527 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9716527 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:20068154 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:9716527 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:9716527 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9716527 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20141003 MGI PMID:20068154 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9716527 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:22615798 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20068154 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0006027 impaired lung alveolus development IAGP N RGD:5509061 20141003 MGI PMID:9716527 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0008168 decreased B-1a cell number IEA N RGD:5509061 20181011 MGI 736645 Fgfr4 fibroblast growth factor receptor 4 gene MP:0010266 decreased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:22615798 736648 Rab3d RAB3D, member RAS oncogene family gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15269275 736648 Rab3d RAB3D, member RAS oncogene family gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15269275 736648 Rab3d RAB3D, member RAS oncogene family gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:15269275 736648 Rab3d RAB3D, member RAS oncogene family gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15269275 736648 Rab3d RAB3D, member RAS oncogene family gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15269275 736648 Rab3d RAB3D, member RAS oncogene family gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15269275 736648 Rab3d RAB3D, member RAS oncogene family gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:16436611 736648 Rab3d RAB3D, member RAS oncogene family gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:15269275 736648 Rab3d RAB3D, member RAS oncogene family gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:16436611 736648 Rab3d RAB3D, member RAS oncogene family gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:16436611 736648 Rab3d RAB3D, member RAS oncogene family gene MP:0003990 decreased neurotransmitter release IAGP N RGD:5509061 20141003 MGI PMID:15269275 736648 Rab3d RAB3D, member RAS oncogene family gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:15269275 736648 Rab3d RAB3D, member RAS oncogene family gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15269275 736648 Rab3d RAB3D, member RAS oncogene family gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15269275 736651 Cryba1 crystallin, beta A1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:10585769 736651 Cryba1 crystallin, beta A1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20161201 MGI PMID:26863613 736651 Cryba1 crystallin, beta A1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20161201 MGI PMID:26863613 736651 Cryba1 crystallin, beta A1 gene MP:0001306 small lens IAGP N RGD:5509061 20161201 MGI PMID:26863613 736651 Cryba1 crystallin, beta A1 gene MP:0002183 gliosis IAGP N RGD:5509061 20150611 MGI PMID:25257511 736651 Cryba1 crystallin, beta A1 gene MP:0002840 abnormal lens fiber morphology IAGP N RGD:5509061 20161201 MGI PMID:26863613 736651 Cryba1 crystallin, beta A1 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20150611 MGI PMID:24468901 736651 Cryba1 crystallin, beta A1 gene MP:0003172 abnormal lysosome physiology IAGP N RGD:5509061 20161201 MGI PMID:26863613 736651 Cryba1 crystallin, beta A1 gene MP:0003237 abnormal lens epithelium morphology IAGP N RGD:5509061 20161201 MGI PMID:26863613 736651 Cryba1 crystallin, beta A1 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20161201 MGI PMID:26863613 736651 Cryba1 crystallin, beta A1 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20150611 MGI PMID:24468901 736651 Cryba1 crystallin, beta A1 gene MP:0005058 abnormal lysosome morphology IAGP N RGD:5509061 20161201 MGI PMID:26863613 736651 Cryba1 crystallin, beta A1 gene MP:0005059 lysosomal protein accumulation IAGP N RGD:5509061 20150611 MGI PMID:25257511 736651 Cryba1 crystallin, beta A1 gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20150611 MGI PMID:24468901 736651 Cryba1 crystallin, beta A1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20150611 MGI PMID:24468901 736651 Cryba1 crystallin, beta A1 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20150611 MGI PMID:25257511 736651 Cryba1 crystallin, beta A1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20161201 MGI PMID:26863613 736651 Cryba1 crystallin, beta A1 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20161201 MGI PMID:26863613 736651 Cryba1 crystallin, beta A1 gene MP:0010254 nuclear cataract IAGP N RGD:5509061 20161201 MGI PMID:26863613 736651 Cryba1 crystallin, beta A1 gene MP:0010263 total cataract IAGP N RGD:5509061 20141003 MGI PMID:10585769 736651 Cryba1 crystallin, beta A1 gene MP:0011628 increased mitochondrial number IAGP N RGD:5509061 20161201 MGI PMID:26863613 736651 Cryba1 crystallin, beta A1 gene MP:0012143 decreased a-wave amplitude IAGP N RGD:5509061 20150611 MGI PMID:24468901 736651 Cryba1 crystallin, beta A1 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20150611 MGI PMID:24468901 736651 Cryba1 crystallin, beta A1 gene MP:0012538 persistent hyaloid artery IAGP N RGD:5509061 20161201 MGI PMID:26863613 736651 Cryba1 crystallin, beta A1 gene MP:0020378 abnormal cell cytoskeleton morphology IAGP N RGD:5509061 20161201 MGI PMID:26863613 736651 Cryba1 crystallin, beta A1 gene MP:0030940 impaired autophagy IAGP N RGD:5509061 20190711 MGI PMID:24468901 736651 Cryba1 crystallin, beta A1 gene MP:0031345 developmental cataract IAGP N RGD:5509061 20220217 MGI PMID:26863613 736651 Cryba1 crystallin, beta A1 gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:25257511 736654 Galr2 galanin receptor 2 gene MP:0001022 abnormal L5 dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:16487144 736654 Galr2 galanin receptor 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:16487144 736654 Galr2 galanin receptor 2 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20111116 MGI 736654 Galr2 galanin receptor 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20150205 MGI PMID:23387435 736654 Galr2 galanin receptor 2 gene MP:0005015 increased T cell number IEA N RGD:5509061 20111116 MGI 736654 Galr2 galanin receptor 2 gene MP:0005017 decreased B cell number IEA N RGD:5509061 20111116 MGI 736654 Galr2 galanin receptor 2 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230119 MGI 736654 Galr2 galanin receptor 2 gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20150205 MGI PMID:23387435 736656 Mst1 macrophage stimulating 1 (hepatocyte growth factor-like) gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9486989 736656 Mst1 macrophage stimulating 1 (hepatocyte growth factor-like) gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:9486989 736656 Mst1 macrophage stimulating 1 (hepatocyte growth factor-like) gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 736656 Mst1 macrophage stimulating 1 (hepatocyte growth factor-like) gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:9486989 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0000434 megacephaly IAGP N RGD:5509061 20210107 MGI PMID:32239694 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20150108 MGI PMID:24719109 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0000859 abnormal somatosensory cortex morphology IAGP N RGD:5509061 20210107 MGI PMID:32239694 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0000905 increased superior colliculus size IAGP N RGD:5509061 20210107 MGI PMID:32239694 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:21156207 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:10854243 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18483067 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20210107 MGI PMID:32239694 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20141003 MGI PMID:16464983 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20141003 MGI PMID:18483067 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16464983 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:18483067 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16464983 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16464983 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18483067 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20150108 MGI PMID:24719109 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20210107 MGI PMID:32239694 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20150108 MGI PMID:24719109 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20160204 MGI PMID:24586341 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:10854243 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:16464983 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20141003 MGI PMID:19060215 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20150108 MGI PMID:24719109 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0003996 clonic seizures IAGP N RGD:5509061 20160204 MGI PMID:24586341 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:16464983 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:18483067 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:21156207 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20150108 MGI PMID:24719109 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20210107 MGI PMID:32239694 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:18483067 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20150108 MGI PMID:24719109 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20150108 MGI PMID:24719109 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:21156207 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:20592205 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18483067 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21156207 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20150108 MGI PMID:24719109 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10854243 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160204 MGI PMID:24586341 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18483067 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18483067 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20210107 MGI PMID:32239694 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0012443 increased corpus callosum size IAGP N RGD:5509061 20210107 MGI PMID:32239694 736658 Kcnq2 potassium voltage-gated channel, subfamily Q, member 2 gene MP:0012448 abnormal primary motor cortex morphology IAGP N RGD:5509061 20210107 MGI PMID:32239694 736661 Colq collagen like tail subunit of asymmetric acetylcholinesterase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10087275 736661 Colq collagen like tail subunit of asymmetric acetylcholinesterase gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:10087275 736661 Colq collagen like tail subunit of asymmetric acetylcholinesterase gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10087275 736661 Colq collagen like tail subunit of asymmetric acetylcholinesterase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10087275 736661 Colq collagen like tail subunit of asymmetric acetylcholinesterase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10087275 736661 Colq collagen like tail subunit of asymmetric acetylcholinesterase gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:10087275 736661 Colq collagen like tail subunit of asymmetric acetylcholinesterase gene MP:0011084 lethality at weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10087275 736667 Kcnj3 potassium inwardly-rectifying channel, subfamily J, member 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 736667 Kcnj3 potassium inwardly-rectifying channel, subfamily J, member 3 gene MP:0001513 limb grasping IEA N RGD:5509061 20160211 MGI 736667 Kcnj3 potassium inwardly-rectifying channel, subfamily J, member 3 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:12374786 736667 Kcnj3 potassium inwardly-rectifying channel, subfamily J, member 3 gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20160811 MGI 736667 Kcnj3 potassium inwardly-rectifying channel, subfamily J, member 3 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:12374786 736667 Kcnj3 potassium inwardly-rectifying channel, subfamily J, member 3 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 736667 Kcnj3 potassium inwardly-rectifying channel, subfamily J, member 3 gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20160811 MGI 736667 Kcnj3 potassium inwardly-rectifying channel, subfamily J, member 3 gene MP:0005574 decreased pulmonary respiratory rate IEA N RGD:5509061 20201022 MGI 736667 Kcnj3 potassium inwardly-rectifying channel, subfamily J, member 3 gene MP:0005575 increased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 736667 Kcnj3 potassium inwardly-rectifying channel, subfamily J, member 3 gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20201022 MGI 736667 Kcnj3 potassium inwardly-rectifying channel, subfamily J, member 3 gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20231207 MGI 736667 Kcnj3 potassium inwardly-rectifying channel, subfamily J, member 3 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 736667 Kcnj3 potassium inwardly-rectifying channel, subfamily J, member 3 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 736669 Cript cysteine-rich PDZ-binding protein gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 736669 Cript cysteine-rich PDZ-binding protein gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IEA N RGD:5509061 20141003 MGI 736669 Cript cysteine-rich PDZ-binding protein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736669 Cript cysteine-rich PDZ-binding protein gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000418 focal hair loss IAGP N RGD:5509061 20141009 MGI PMID:24352790 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20141003 MGI PMID:24283265 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20141003 MGI PMID:11242117 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11242118 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15492925 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17289941 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23452848 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000745 tremors IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:11242118 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23452848 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:20163734 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20141003 MGI PMID:23452848 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:20163734 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:16446138 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:20163734 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:20163734 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20163734 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:23452848 736671 Mecp2 methyl CpG binding protein 2 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141009 MGI PMID:24352790 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:17936729 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11242117 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18321864 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18321865 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19225110 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23452848 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20160324 MGI PMID:25634563 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:11242118 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:17289941 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:17936729 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:18321865 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001261 obese IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11242117 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15069197 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20869373 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24283265 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160128 MGI PMID:26647311 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160324 MGI PMID:25634563 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11242117 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:18321864 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:18321865 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20141009 MGI PMID:24352790 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001360 abnormal social investigation IAGP N RGD:5509061 20160304 MGI PMID:26590342 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:24283265 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:18321864 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141009 MGI PMID:24352790 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20160128 MGI PMID:26647311 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20160324 MGI PMID:25634563 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11242118 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20633611 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20160304 MGI PMID:26590342 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:19225110 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11242117 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:11242118 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15069197 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:15492925 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:17936729 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:19225110 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20869373 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23770565 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:24283265 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20201210 MGI PMID:32469049 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18321864 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:18557922 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:20869373 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23770565 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23770587 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:24283265 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160304 MGI PMID:26590342 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20160324 MGI PMID:25634563 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20201210 MGI PMID:32469049 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11242117 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20633611 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23452848 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141009 MGI PMID:24352790 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160304 MGI PMID:26590342 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20201210 MGI PMID:32469049 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:20633611 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20201210 MGI PMID:32469049 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001408 stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:15492925 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:17936729 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20160304 MGI PMID:26590342 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141009 MGI PMID:24352790 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:18321864 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18321864 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18321864 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17289941 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20160324 MGI PMID:25634563 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:18321864 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20160304 MGI PMID:26590342 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20141003 MGI PMID:11242118 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001511 disheveled coat IAGP N RGD:5509061 20141003 MGI PMID:23452848 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:11242117 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:17289941 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:17936729 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:18321865 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:23770565 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:23770587 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141009 MGI PMID:24352790 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:18321865 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20160324 MGI PMID:25634563 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:22375006 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20163734 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001926 female infertility IEA N RGD:5509061 20180614 MGI 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:11242118 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20141003 MGI PMID:24283265 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:11242117 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:17289941 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:17936729 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:18321864 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:22302819 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20201210 MGI PMID:32469049 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:18321864 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001957 apnea IAGP N RGD:5509061 20141003 MGI PMID:22302819 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001957 apnea IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001957 apnea IAGP N RGD:5509061 20201210 MGI PMID:32469049 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001963 abnormal hearing physiology IAGP N RGD:5509061 20141003 MGI PMID:11242117 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:18321864 736671 Mecp2 methyl CpG binding protein 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:18321864 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141009 MGI PMID:24352790 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002064 seizures IAGP N RGD:5509061 20160304 MGI PMID:26590342 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002064 seizures IAGP N RGD:5509061 20201210 MGI PMID:32469049 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002065 abnormal fear/anxiety-related behavior IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:11242117 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20160128 MGI PMID:26647311 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11242117 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11242118 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15492925 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16446138 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17289941 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17936729 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20869373 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23452848 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23770565 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141009 MGI PMID:24352790 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20160128 MGI PMID:26647311 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20160304 MGI PMID:26590342 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20160324 MGI PMID:25634563 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20201210 MGI PMID:32469049 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002083 premature death IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002098 abnormal vibrissa morphology IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002100 abnormal tooth morphology IAGP N RGD:5509061 20141003 MGI PMID:11242117 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:11242118 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:15069197 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:16446138 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:23452848 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:23770565 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:23770587 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20160324 MGI PMID:25634563 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002176 increased brain weight IAGP N RGD:5509061 20141003 MGI PMID:19225110 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002204 abnormal synaptic neurotransmitter level IAGP N RGD:5509061 20141003 MGI PMID:20633611 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:11242117 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:18321864 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002690 akinesia IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:18557922 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20160128 MGI PMID:26647311 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20201210 MGI PMID:32469049 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20160324 MGI PMID:25634563 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11242118 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:23770587 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20160324 MGI PMID:25634563 736671 Mecp2 methyl CpG binding protein 2 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20160324 MGI PMID:25634563 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003107 abnormal response to novelty IAGP N RGD:5509061 20141003 MGI PMID:21982370 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:11242118 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20160324 MGI PMID:25634563 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:20633611 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:20633611 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:24283265 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:21982370 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20170504 MGI PMID:24735673 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003646 increased muscle fatigability IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003849 greasy coat IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003928 increased heart rate variability IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:24283265 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20160304 MGI PMID:26590342 736671 Mecp2 methyl CpG binding protein 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20160324 MGI PMID:25634563 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004085 abnormal heartbeat IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004170 abnormal orbitofrontal cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:20163734 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004183 abnormal sympathetic nervous system physiology IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:17920015 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:11242118 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:12160743 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:17289941 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:23770565 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141009 MGI PMID:24352790 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20160128 MGI PMID:26647311 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20201210 MGI PMID:32469049 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:17920015 736671 Mecp2 methyl CpG binding protein 2 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:11242118 736671 Mecp2 methyl CpG binding protein 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:16446138 736671 Mecp2 methyl CpG binding protein 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:16467389 736671 Mecp2 methyl CpG binding protein 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:24283265 736671 Mecp2 methyl CpG binding protein 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:16446138 736671 Mecp2 methyl CpG binding protein 2 gene MP:0005426 tachypnea IAGP N RGD:5509061 20141003 MGI PMID:22302819 736671 Mecp2 methyl CpG binding protein 2 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0005535 abnormal body temperature IAGP N RGD:5509061 20141003 MGI PMID:11242118 736671 Mecp2 methyl CpG binding protein 2 gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20160324 MGI PMID:25634563 736671 Mecp2 methyl CpG binding protein 2 gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20201210 MGI PMID:32469049 736671 Mecp2 methyl CpG binding protein 2 gene MP:0005586 decreased tidal volume IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0006277 abnormal parasympathetic nervous system physiology IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:20163734 736671 Mecp2 methyl CpG binding protein 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:21982370 736671 Mecp2 methyl CpG binding protein 2 gene MP:0008265 abnormal hippocampus CA2 region morphology IAGP N RGD:5509061 20141003 MGI PMID:11242118 736671 Mecp2 methyl CpG binding protein 2 gene MP:0008265 abnormal hippocampus CA2 region morphology IAGP N RGD:5509061 20141003 MGI PMID:16446138 736671 Mecp2 methyl CpG binding protein 2 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:17936729 736671 Mecp2 methyl CpG binding protein 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:18321865 736671 Mecp2 methyl CpG binding protein 2 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:16549272 736671 Mecp2 methyl CpG binding protein 2 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009141 increased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20141003 MGI PMID:18321864 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20201210 MGI PMID:32469049 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20160324 MGI PMID:25634563 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20201210 MGI PMID:32469049 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20160304 MGI PMID:26590342 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20201210 MGI PMID:32469049 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009658 increased placenta apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22375006 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009939 abnormal hippocampus neuron morphology IAGP N RGD:5509061 20141009 MGI PMID:24352790 736671 Mecp2 methyl CpG binding protein 2 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22119903 736671 Mecp2 methyl CpG binding protein 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:24283265 736671 Mecp2 methyl CpG binding protein 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20220519 MGI PMID:30402709 736671 Mecp2 methyl CpG binding protein 2 gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20141003 MGI PMID:20633611 736671 Mecp2 methyl CpG binding protein 2 gene MP:0010162 increased brain cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23892605 736671 Mecp2 methyl CpG binding protein 2 gene MP:0010382 abnormal dosage compensation, by inactivation of X chromosome IAGP N RGD:5509061 20141003 MGI PMID:16549272 736671 Mecp2 methyl CpG binding protein 2 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20171221 MGI PMID:28159985 736671 Mecp2 methyl CpG binding protein 2 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22375006 736671 Mecp2 methyl CpG binding protein 2 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:17920015 736671 Mecp2 methyl CpG binding protein 2 gene MP:0012006 abnormal hippocampus physiology IAGP N RGD:5509061 20170504 MGI PMID:24735673 736671 Mecp2 methyl CpG binding protein 2 gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20180927 MGI PMID:20633611 736671 Mecp2 methyl CpG binding protein 2 gene MP:0014274 decreased respiration IAGP N RGD:5509061 20230810 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:24283265 736671 Mecp2 methyl CpG binding protein 2 gene MP:0014376 decreased miniature excitatory postsynaptic current frequency IAGP N RGD:5509061 20240418 MGI PMID:17920015 736671 Mecp2 methyl CpG binding protein 2 gene MP:0014384 increased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:21982370 736671 Mecp2 methyl CpG binding protein 2 gene MP:0014385 decreased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:21068835 736671 Mecp2 methyl CpG binding protein 2 gene MP:0020870 decreased thigmotaxis IAGP N RGD:5509061 20201210 MGI PMID:32469049 736676 Sqle squalene epoxidase gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:23892605 736676 Sqle squalene epoxidase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:23892605 736676 Sqle squalene epoxidase gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:23892605 736676 Sqle squalene epoxidase gene MP:0001259 abnormal body weight IAGP N RGD:5509061 20141003 MGI PMID:23892605 736676 Sqle squalene epoxidase gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:23892605 736676 Sqle squalene epoxidase gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20141003 MGI PMID:23892605 736676 Sqle squalene epoxidase gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:23892605 736676 Sqle squalene epoxidase gene MP:0001661 extended life span IAGP N RGD:5509061 20141003 MGI PMID:23892605 736676 Sqle squalene epoxidase gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:23892605 736676 Sqle squalene epoxidase gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 736676 Sqle squalene epoxidase gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:23892605 736676 Sqle squalene epoxidase gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:23892605 736676 Sqle squalene epoxidase gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23892605 736676 Sqle squalene epoxidase gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 736676 Sqle squalene epoxidase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736678 Sult4a1 sulfotransferase family 4A, member 1 gene MP:0000745 tremors IAGP N RGD:5509061 20191128 MGI PMID:29109113 736678 Sult4a1 sulfotransferase family 4A, member 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20191128 MGI PMID:29109113 736678 Sult4a1 sulfotransferase family 4A, member 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20191128 MGI PMID:29109113 736678 Sult4a1 sulfotransferase family 4A, member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20191128 MGI PMID:29109113 736678 Sult4a1 sulfotransferase family 4A, member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20191128 MGI PMID:29109113 736678 Sult4a1 sulfotransferase family 4A, member 1 gene MP:0003216 absence seizures IAGP N RGD:5509061 20191128 MGI PMID:29109113 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0000688 lymphoid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:22200760 736682 Mtus1 mitochondrial tumor suppressor 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22200760 736683 Cd46 CD46 antigen, complement regulatory protein gene MP:0001004 abnormal retina photoreceptor morphology IAGP N RGD:5509061 20170615 MGI PMID:27295359 736683 Cd46 CD46 antigen, complement regulatory protein gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141030 MGI PMID:25019227 736683 Cd46 CD46 antigen, complement regulatory protein gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20170615 MGI PMID:27295359 736683 Cd46 CD46 antigen, complement regulatory protein gene MP:0001934 increased litter size IAGP N RGD:5509061 20141003 MGI PMID:12640142 736683 Cd46 CD46 antigen, complement regulatory protein gene MP:0003731 abnormal retina outer nuclear layer morphology IAGP N RGD:5509061 20170615 MGI PMID:27295359 736683 Cd46 CD46 antigen, complement regulatory protein gene MP:0005098 abnormal optic choroid morphology IAGP N RGD:5509061 20170615 MGI PMID:27295359 736683 Cd46 CD46 antigen, complement regulatory protein gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20170615 MGI PMID:27295359 736683 Cd46 CD46 antigen, complement regulatory protein gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20170615 MGI PMID:27295359 736683 Cd46 CD46 antigen, complement regulatory protein gene MP:0005410 abnormal fertilization IAGP N RGD:5509061 20141003 MGI PMID:12640142 736683 Cd46 CD46 antigen, complement regulatory protein gene MP:0006238 abnormal choriocapillaris morphology IAGP N RGD:5509061 20170615 MGI PMID:27295359 736683 Cd46 CD46 antigen, complement regulatory protein gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20170615 MGI PMID:27295359 736683 Cd46 CD46 antigen, complement regulatory protein gene MP:0011557 increased susceptibility to induced choroid neovascularization IAGP N RGD:5509061 20141030 MGI PMID:25019227 736683 Cd46 CD46 antigen, complement regulatory protein gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:27295359 736686 Hsbp1 heat shock factor binding protein 1 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141030 MGI PMID:24380799 736686 Hsbp1 heat shock factor binding protein 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141030 MGI PMID:24380799 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16597604 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:10508513 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:10508513 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15123655 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0001203 increased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:12499274 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0001204 decreased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:12499274 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16141330 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16141330 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16141330 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16141330 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:16170381 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0002607 decreased basophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0003111 abnormal cell nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:10508513 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0003702 abnormal chromosome morphology IAGP N RGD:5509061 20141003 MGI PMID:10508513 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15123655 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0004023 abnormal chromosome number IAGP N RGD:5509061 20141003 MGI PMID:10508513 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:10508513 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:15123655 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0004046 abnormal mitosis IAGP N RGD:5509061 20141003 MGI PMID:10508513 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0004500 increased incidence of tumors by ionizing radiation induction IAGP N RGD:5509061 20141003 MGI PMID:10508513 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0004501 increased incidence of tumors by UV-induction IAGP N RGD:5509061 20141003 MGI PMID:12499274 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0004759 decreased mitotic index IAGP N RGD:5509061 20141003 MGI PMID:10508513 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:10508513 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0005012 decreased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10508513 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0008014 increased lung tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16141330 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0008411 decreased cellular sensitivity to ultraviolet irradiation IAGP N RGD:5509061 20141003 MGI PMID:15917306 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0009796 abnormal base-excision repair IAGP N RGD:5509061 20141003 MGI PMID:15917306 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15123655 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0011440 increased kidney cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0011453 abnormal glomerular capillary endothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0011512 mesangial cell interposition IAGP N RGD:5509061 20141003 MGI PMID:11970874 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0011703 increased fibroblast proliferation IAGP N RGD:5509061 20150219 MGI PMID:10508513 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0012010 parturition failure IAGP N RGD:5509061 20141003 MGI PMID:10508513 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:10508513 736689 Gadd45a growth arrest and DNA-damage-inducible 45 alpha gene MP:0030943 abnormal centrosome morphology IAGP N RGD:5509061 20190718 MGI PMID:15123655 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20201022 MGI 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0000559 abnormal femur morphology IEA N RGD:5509061 20170105 MGI 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20240229 MGI PMID:33439101 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0001762 polyuria IAGP N RGD:5509061 20240229 MGI PMID:36722887 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20240229 MGI PMID:33439101 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20240229 MGI PMID:33439101 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20240229 MGI PMID:36722887 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20240229 MGI PMID:33439101 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20201022 MGI 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20200402 MGI 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20201022 MGI 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0008055 increased urine osmolality IAGP N RGD:5509061 20240229 MGI PMID:36722887 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20240229 MGI PMID:36722887 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0012605 decreased kidney glutathione level IAGP N RGD:5509061 20240229 MGI PMID:36722887 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0012659 decreased superoxide dismutase level IAGP N RGD:5509061 20240229 MGI PMID:36722887 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0014359 increased ferroptosis IAGP N RGD:5509061 20240229 MGI PMID:36722887 736695 Slc38a2 solute carrier family 38, member 2 gene MP:0014525 impaired pulmonary alveolar fluid clearance IAGP N RGD:5509061 20240912 MGI PMID:33439101 736697 Aplp1 amyloid beta precursor like protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11050115 736697 Aplp1 amyloid beta precursor like protein 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11050115 736703 Cd5 CD5 antigen gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20170105 MGI 736703 Cd5 CD5 antigen gene MP:0000691 enlarged spleen IEA N RGD:5509061 20170105 MGI 736703 Cd5 CD5 antigen gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 736703 Cd5 CD5 antigen gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20170105 MGI 736703 Cd5 CD5 antigen gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:7517879 736703 Cd5 CD5 antigen gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210128 MGI 736703 Cd5 CD5 antigen gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0005002 abnormal T cell clonal deletion IAGP N RGD:5509061 20141003 MGI PMID:11342622 736703 Cd5 CD5 antigen gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11342622 736703 Cd5 CD5 antigen gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11342622 736703 Cd5 CD5 antigen gene MP:0008087 decreased T helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0008747 abnormal T cell anergy IAGP N RGD:5509061 20141003 MGI PMID:22904299 736703 Cd5 CD5 antigen gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:22904299 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0000708 thymus hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0008081 abnormal single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21048919 736708 Adrm1 adhesion regulating molecule 1 26S proteasome ubiquitin receptor gene MP:0011122 absent primordial ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:21048919 736709 Bambi BMP and activin membrane-bound inhibitor gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 736709 Bambi BMP and activin membrane-bound inhibitor gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20181227 MGI 736709 Bambi BMP and activin membrane-bound inhibitor gene MP:0001147 small testis IEA N RGD:5509061 20181227 MGI 736709 Bambi BMP and activin membrane-bound inhibitor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17661381 736709 Bambi BMP and activin membrane-bound inhibitor gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:20107078 736709 Bambi BMP and activin membrane-bound inhibitor gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:20107078 736709 Bambi BMP and activin membrane-bound inhibitor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17661381 736709 Bambi BMP and activin membrane-bound inhibitor gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:20107078 736709 Bambi BMP and activin membrane-bound inhibitor gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:20107078 736709 Bambi BMP and activin membrane-bound inhibitor gene MP:0009709 hydrometra IEA N RGD:5509061 20210520 MGI 736709 Bambi BMP and activin membrane-bound inhibitor gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 736710 Trp63 transformation related protein 63 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:23108156 736710 Trp63 transformation related protein 63 gene MP:0000111 cleft palate IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0000111 cleft palate IAGP N RGD:5509061 20220714 MGI PMID:25358290 736710 Trp63 transformation related protein 63 gene MP:0000116 abnormal tooth development IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0000117 absent tooth placode IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20141003 MGI PMID:11857801 736710 Trp63 transformation related protein 63 gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20141003 MGI PMID:22274697 736710 Trp63 transformation related protein 63 gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20181129 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0000414 alopecia IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0000420 ruffled hair IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:12368184 736710 Trp63 transformation related protein 63 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:18326838 736710 Trp63 transformation related protein 63 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23620512 736710 Trp63 transformation related protein 63 gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:23620512 736710 Trp63 transformation related protein 63 gene MP:0000469 abnormal esophageal squamous epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0000469 abnormal esophageal squamous epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15189821 736710 Trp63 transformation related protein 63 gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21703447 736710 Trp63 transformation related protein 63 gene MP:0000472 abnormal stomach non-glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0000492 abnormal rectum morphology IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0000493 rectal prolapse IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:17079275 736710 Trp63 transformation related protein 63 gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12368193 736710 Trp63 transformation related protein 63 gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17079275 736710 Trp63 transformation related protein 63 gene MP:0000540 abnormal urinary bladder urothelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0000543 absent urinary bladder urothelium IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0000543 absent urinary bladder urothelium IAGP N RGD:5509061 20141003 MGI PMID:17079275 736710 Trp63 transformation related protein 63 gene MP:0000544 thin urinary bladder urothelium IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0000547 short limbs IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:12368184 736710 Trp63 transformation related protein 63 gene MP:0000549 absent limbs IAGP N RGD:5509061 20141003 MGI PMID:23620512 736710 Trp63 transformation related protein 63 gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0000553 absent radius IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0000553 absent radius IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0000555 absent carpal bone IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0000555 absent carpal bone IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:11857801 736710 Trp63 transformation related protein 63 gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:18326838 736710 Trp63 transformation related protein 63 gene MP:0000561 adactyly IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:18326838 736710 Trp63 transformation related protein 63 gene MP:0000614 absent salivary gland IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0000629 absent mammary gland IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0000648 absent sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0000648 absent sebaceous gland IAGP N RGD:5509061 20141003 MGI PMID:22274697 736710 Trp63 transformation related protein 63 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0000764 abnormal tongue epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0000766 absent tongue squamous epithelium IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:12368184 736710 Trp63 transformation related protein 63 gene MP:0001137 abnormal uterine cervix epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0001137 abnormal uterine cervix epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0001140 abnormal vagina epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0001159 absent prostate gland IAGP N RGD:5509061 20141003 MGI PMID:11106548 736710 Trp63 transformation related protein 63 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0001201 translucent skin IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:23108156 736710 Trp63 transformation related protein 63 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:24449888 736710 Trp63 transformation related protein 63 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23108156 736710 Trp63 transformation related protein 63 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24449888 736710 Trp63 transformation related protein 63 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0001217 absent epidermis IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0001217 absent epidermis IAGP N RGD:5509061 20141003 MGI PMID:12368184 736710 Trp63 transformation related protein 63 gene MP:0001217 absent epidermis IAGP N RGD:5509061 20141003 MGI PMID:22274697 736710 Trp63 transformation related protein 63 gene MP:0001217 absent epidermis IAGP N RGD:5509061 20141003 MGI PMID:23620512 736710 Trp63 transformation related protein 63 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:24449888 736710 Trp63 transformation related protein 63 gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20141003 MGI PMID:24449888 736710 Trp63 transformation related protein 63 gene MP:0001241 absent epidermis stratum corneum IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0001341 absent eyelids IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0001394 circling IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:22274697 736710 Trp63 transformation related protein 63 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:22274697 736710 Trp63 transformation related protein 63 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0001675 abnormal ectoderm development IAGP N RGD:5509061 20141003 MGI PMID:18326838 736710 Trp63 transformation related protein 63 gene MP:0001676 abnormal apical ectodermal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:18326838 736710 Trp63 transformation related protein 63 gene MP:0001677 absent apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0001677 absent apical ectodermal ridge IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0001874 acanthosis IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0002018 increased malignant tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0002036 increased rhabdomyosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0002048 increased lung adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:21677159 736710 Trp63 transformation related protein 63 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:21677159 736710 Trp63 transformation related protein 63 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:17079275 736710 Trp63 transformation related protein 63 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11857801 736710 Trp63 transformation related protein 63 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23620512 736710 Trp63 transformation related protein 63 gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15189821 736710 Trp63 transformation related protein 63 gene MP:0002406 increased susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:12368184 736710 Trp63 transformation related protein 63 gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22274697 736710 Trp63 transformation related protein 63 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:22274697 736710 Trp63 transformation related protein 63 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0003125 abnormal septation of the cloaca IAGP N RGD:5509061 20141003 MGI PMID:12368184 736710 Trp63 transformation related protein 63 gene MP:0003160 abnormal esophagus development IAGP N RGD:5509061 20141003 MGI PMID:15189821 736710 Trp63 transformation related protein 63 gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20141003 MGI PMID:17079275 736710 Trp63 transformation related protein 63 gene MP:0003320 rectovaginal fistula IAGP N RGD:5509061 20141003 MGI PMID:12368184 736710 Trp63 transformation related protein 63 gene MP:0003384 abnormal ventral body wall morphology IAGP N RGD:5509061 20141003 MGI PMID:12368184 736710 Trp63 transformation related protein 63 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22274697 736710 Trp63 transformation related protein 63 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:23108156 736710 Trp63 transformation related protein 63 gene MP:0003453 abnormal keratinocyte physiology IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0003575 absent oviduct IAGP N RGD:5509061 20141003 MGI PMID:12368184 736710 Trp63 transformation related protein 63 gene MP:0003578 absent ovary IAGP N RGD:5509061 20141003 MGI PMID:12368184 736710 Trp63 transformation related protein 63 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0003789 increased osteosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0003800 monodactyly IAGP N RGD:5509061 20141003 MGI PMID:18326838 736710 Trp63 transformation related protein 63 gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141003 MGI PMID:22274697 736710 Trp63 transformation related protein 63 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20141003 MGI PMID:22274697 736710 Trp63 transformation related protein 63 gene MP:0003941 abnormal skin development IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0004024 aneuploidy IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0004033 supernumerary teeth IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:22274697 736710 Trp63 transformation related protein 63 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0004228 decreased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17122775 736710 Trp63 transformation related protein 63 gene MP:0004360 absent ulna IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0004540 small maxilla IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0004575 small limb buds IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0004575 small limb buds IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0004575 small limb buds IAGP N RGD:5509061 20141003 MGI PMID:18326838 736710 Trp63 transformation related protein 63 gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0004684 intervertebral disk degeneration IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0005034 abnormal anus morphology IAGP N RGD:5509061 20141003 MGI PMID:17079275 736710 Trp63 transformation related protein 63 gene MP:0005213 gastric metaplasia IAGP N RGD:5509061 20141003 MGI PMID:21703447 736710 Trp63 transformation related protein 63 gene MP:0005230 ectrodactyly IAGP N RGD:5509061 20141003 MGI PMID:18326838 736710 Trp63 transformation related protein 63 gene MP:0005230 ectrodactyly IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:18326838 736710 Trp63 transformation related protein 63 gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0005494 esophagogastric junction metaplasia IAGP N RGD:5509061 20141003 MGI PMID:21703447 736710 Trp63 transformation related protein 63 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0006000 abnormal cornea epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:17079275 736710 Trp63 transformation related protein 63 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17079275 736710 Trp63 transformation related protein 63 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21982646 736710 Trp63 transformation related protein 63 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:22274697 736710 Trp63 transformation related protein 63 gene MP:0008007 abnormal cellular replicative senescence IAGP N RGD:5509061 20150305 MGI PMID:19898465 736710 Trp63 transformation related protein 63 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0008008 early cellular replicative senescence IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21677159 736710 Trp63 transformation related protein 63 gene MP:0008866 chromosomal instability IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0009101 clitoris hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12368184 736710 Trp63 transformation related protein 63 gene MP:0009228 uterine cervix inflammation IAGP N RGD:5509061 20141003 MGI PMID:16107615 736710 Trp63 transformation related protein 63 gene MP:0009321 increased histiocytic sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0009474 thick epidermis stratum spinosum IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0009551 increased urinary bladder transitional cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0009560 absent epidermis stratum granulosum IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22274697 736710 Trp63 transformation related protein 63 gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0009614 absent epidermis stratum spinosum IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20220714 MGI PMID:25358290 736710 Trp63 transformation related protein 63 gene MP:0009715 thick epidermis stratum basale IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0009736 abnormal prostate gland branching morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:11106548 736710 Trp63 transformation related protein 63 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0010116 abnormal primitive urogenital sinus morphology IAGP N RGD:5509061 20141003 MGI PMID:17079275 736710 Trp63 transformation related protein 63 gene MP:0010146 umbilical hernia IAGP N RGD:5509061 20141003 MGI PMID:17079275 736710 Trp63 transformation related protein 63 gene MP:0010787 gastric cyst IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0010942 abnormal respiratory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15189821 736710 Trp63 transformation related protein 63 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10227294 736710 Trp63 transformation related protein 63 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22274697 736710 Trp63 transformation related protein 63 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23108156 736710 Trp63 transformation related protein 63 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24449888 736710 Trp63 transformation related protein 63 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20160128 MGI 736710 Trp63 transformation related protein 63 gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19570515 736710 Trp63 transformation related protein 63 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0011160 dermal-epidermal separation IAGP N RGD:5509061 20141003 MGI PMID:24449888 736710 Trp63 transformation related protein 63 gene MP:0011774 abnormal urinary bladder detrusor smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17079275 736710 Trp63 transformation related protein 63 gene MP:0012062 small tail bud IAGP N RGD:5509061 20141003 MGI PMID:12368184 736710 Trp63 transformation related protein 63 gene MP:0012067 abnormal olfactory gland morphology IAGP N RGD:5509061 20141120 MGI PMID:21677159 736710 Trp63 transformation related protein 63 gene MP:0012069 abnormal horizontal basal cell of olfactory epithelium morphology IAGP N RGD:5509061 20160407 MGI PMID:21677159 736710 Trp63 transformation related protein 63 gene MP:0012400 nail dystrophy IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0013282 urinary bladder exstrophy IAGP N RGD:5509061 20141003 MGI PMID:17079275 736710 Trp63 transformation related protein 63 gene MP:0013530 abnormal periderm morphology IAGP N RGD:5509061 20220714 MGI PMID:25358290 736710 Trp63 transformation related protein 63 gene MP:0013537 increased salivary gland adenoma incidence IAGP N RGD:5509061 20150219 MGI PMID:15837625 736710 Trp63 transformation related protein 63 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:11857801 736710 Trp63 transformation related protein 63 gene MP:0014321 short forelimb IAGP N RGD:5509061 20231130 MGI PMID:18326838 736710 Trp63 transformation related protein 63 gene MP:0020823 absent pubic symphysis IAGP N RGD:5509061 20181018 MGI PMID:17079275 736710 Trp63 transformation related protein 63 gene MP:0030493 abnormal tooth root morphology IAGP N RGD:5509061 20201217 MGI PMID:23775923 736710 Trp63 transformation related protein 63 gene MP:0030610 absent teeth IAGP N RGD:5509061 20180726 MGI PMID:10227293 736710 Trp63 transformation related protein 63 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:16107615 736713 Myog myogenin gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:10694423 736713 Myog myogenin gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:10075840 736713 Myog myogenin gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10075840 736713 Myog myogenin gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10694423 736713 Myog myogenin gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:10696067 736713 Myog myogenin gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:7532173 736713 Myog myogenin gene MP:0000729 abnormal myogenesis IAGP N RGD:5509061 20141003 MGI PMID:9609818 736713 Myog myogenin gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:10694423 736713 Myog myogenin gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:7532173 736713 Myog myogenin gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10075840 736713 Myog myogenin gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10694423 736713 Myog myogenin gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10696067 736713 Myog myogenin gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7532173 736713 Myog myogenin gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8393146 736713 Myog myogenin gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9609818 736713 Myog myogenin gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:10696067 736713 Myog myogenin gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:16407395 736713 Myog myogenin gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:10696067 736713 Myog myogenin gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:10696067 736713 Myog myogenin gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16407395 736713 Myog myogenin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16407395 736713 Myog myogenin gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:10696067 736713 Myog myogenin gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10696067 736713 Myog myogenin gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:10075840 736713 Myog myogenin gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10696067 736713 Myog myogenin gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:10696067 736713 Myog myogenin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14966278 736713 Myog myogenin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9609818 736713 Myog myogenin gene MP:0002263 abnormal laryngeal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10696067 736713 Myog myogenin gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9609818 736713 Myog myogenin gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:10694423 736713 Myog myogenin gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:9609818 736713 Myog myogenin gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:10075840 736713 Myog myogenin gene MP:0004321 short sternum IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0004322 abnormal sternebra morphology IAGP N RGD:5509061 20141003 MGI PMID:9609818 736713 Myog myogenin gene MP:0004672 short ribs IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0008148 abnormal sternocostal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:9609818 736713 Myog myogenin gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0009408 decreased skeletal muscle fiber density IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16407395 736713 Myog myogenin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10075840 736713 Myog myogenin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10694423 736713 Myog myogenin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10696067 736713 Myog myogenin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8393145 736713 Myog myogenin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8393146 736713 Myog myogenin gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9609818 736713 Myog myogenin gene MP:0011808 abnormal myoblast differentiation IAGP N RGD:5509061 20190725 MGI PMID:7532173 736713 Myog myogenin gene MP:0012280 abnormal sternebra size IAGP N RGD:5509061 20141003 MGI PMID:8393145 736714 Pnck pregnancy upregulated non-ubiquitously expressed CaM kinase gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 736714 Pnck pregnancy upregulated non-ubiquitously expressed CaM kinase gene MP:0005574 decreased pulmonary respiratory rate IEA N RGD:5509061 20211021 MGI 736714 Pnck pregnancy upregulated non-ubiquitously expressed CaM kinase gene MP:0005576 decreased pulmonary ventilation IEA N RGD:5509061 20210128 MGI 736714 Pnck pregnancy upregulated non-ubiquitously expressed CaM kinase gene MP:0005586 decreased tidal volume IEA N RGD:5509061 20211021 MGI 736714 Pnck pregnancy upregulated non-ubiquitously expressed CaM kinase gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20230720 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000024 lowered ear position IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000075 absent neurocranium IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:24355925 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000276 heart right ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000519 hydronephrosis IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:24355925 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000913 abnormal brain development IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:10664446 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:10852901 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:10664446 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:18077586 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20141003 MGI PMID:18077586 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001347 absent lacrimal glands IAGP N RGD:5509061 20141003 MGI PMID:22745308 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10664446 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10852901 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16056228 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001890 anencephaly IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10852901 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:10664446 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:18077586 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:10664446 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:24355925 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0002625 heart left ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0002633 persistent truncus arteriosus IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0002659 pituitary gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0003052 omphalocele IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:16056228 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:16056228 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0003675 kidney cyst IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:24355925 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0004133 heterotaxia IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0004157 interrupted aortic arch IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0004158 right aortic arch IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:10664446 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:10852901 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:24355925 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0005274 abnormal viscerocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:24355925 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0006290 proboscis IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0008221 abnormal hippocampal commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0008225 abnormal anterior commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0009880 decreased mouth size IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0009898 maxillary shelf hypoplasia IAGP N RGD:5509061 20171109 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0009905 absent tongue IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:19889634 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0010466 vascular ring IEA N RGD:5509061 20141003 MGI 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0010714 iris coloboma IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0010890 decreased alveolar lamellar body number IAGP N RGD:5509061 20141003 MGI PMID:10664446 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0010912 herniated liver IAGP N RGD:5509061 20141003 MGI PMID:24355925 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10664446 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10852901 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16056228 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10852901 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:24355925 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0011708 decreased fibroblast cell migration IAGP N RGD:5509061 20141003 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0012061 abnormal diaphragm central tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:24355925 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0012201 decreased endothelial cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24355925 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0012252 abnormal septum transversum morphology IAGP N RGD:5509061 20141003 MGI PMID:24355925 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0012261 increased hindbrain apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0013331 abnormal lacrimal gland development IAGP N RGD:5509061 20141204 MGI PMID:18077586 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0013331 abnormal lacrimal gland development IAGP N RGD:5509061 20141204 MGI PMID:22745308 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0014155 absent olfactory epithelium IAGP N RGD:5509061 20160407 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:16056228 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0030190 small snout IAGP N RGD:5509061 20171019 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0030250 frontonasal prominence hypoplasia IAGP N RGD:5509061 20171019 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0030250 frontonasal prominence hypoplasia IAGP N RGD:5509061 20171019 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0030313 abnormal face development IAGP N RGD:5509061 20171109 MGI PMID:18385133 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0030385 absent facial bone IAGP N RGD:5509061 20171207 MGI PMID:16020517 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0030803 abnormal tendon cell morphology IAGP N RGD:5509061 20181011 MGI PMID:24355925 736720 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 gene MP:0031445 midline cleft upper lip IAGP N RGD:5509061 20221103 MGI PMID:16020517 736726 Sec14l2 SEC14-like lipid binding 2 gene MP:0005146 decreased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17077281 736726 Sec14l2 SEC14-like lipid binding 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:17077281 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0000160 kyphosis IAGP N RGD:5509061 20170525 MGI PMID:26642438 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:24784230 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:24784230 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:24784230 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20170525 MGI PMID:26642438 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:17015831 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0001513 limb grasping IAGP N RGD:5509061 20170525 MGI PMID:26642438 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:17015831 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20170525 MGI PMID:26642438 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20170525 MGI PMID:26642438 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:24784230 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:17015831 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0002888 abnormal NMDA-mediated synaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17015831 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17015831 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10676965 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:10676965 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17015831 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0008462 abnormal medium spiny neuron morphology IAGP N RGD:5509061 20170525 MGI PMID:26642438 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20170525 MGI PMID:26642438 736730 Rgs9 regulator of G-protein signaling 9 gene MP:0012508 forebrain atrophy IAGP N RGD:5509061 20141003 MGI PMID:24784230 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:12441290 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:12441290 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000558 abnormal tibia morphology IAGP N RGD:5509061 20141003 MGI PMID:12441290 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000559 abnormal femur morphology IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:12441290 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000572 abnormal autopod morphology IEA N RGD:5509061 20181227 MGI 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000576 clubfoot IAGP N RGD:5509061 20141003 MGI PMID:21775501 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000579 abnormal nail morphology IEA N RGD:5509061 20201231 MGI 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21775501 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20210520 MGI 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:21775501 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0002110 abnormal digit morphology IEA N RGD:5509061 20181227 MGI 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:12441290 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21775501 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0002728 absent tibia IAGP N RGD:5509061 20141003 MGI PMID:12441290 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0002932 abnormal joint morphology IEA N RGD:5509061 20210520 MGI 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0003036 vertebral transformation IEA N RGD:5509061 20210520 MGI 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:12441290 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0004083 polysyndactyly IEA N RGD:5509061 20210520 MGI 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0004349 absent femur IAGP N RGD:5509061 20141003 MGI PMID:12441290 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12441290 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0004575 small limb buds IAGP N RGD:5509061 20141003 MGI PMID:12441290 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0004688 absent ilium IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0004688 absent ilium IAGP N RGD:5509061 20141003 MGI PMID:12441290 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0004689 small ischium IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0004692 small pubis IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0004694 absent patella IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0004694 absent patella IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0005452 abnormal adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:21775501 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0006020 decreased tympanic ring size IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0008335 decreased gonadotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0008338 decreased thyrotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0008381 absent gonial bone IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0008730 fused phalanges IEA N RGD:5509061 20181227 MGI 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0009524 absent submandibular gland IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0009910 bifurcated tongue IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:21775501 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0013169 small hindlimb buds IAGP N RGD:5509061 20141003 MGI PMID:12441290 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0013349 small Rathke's pouch IAGP N RGD:5509061 20141218 MGI PMID:11807026 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:11807026 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:12441290 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0014322 short hindlimb IAGP N RGD:5509061 20231130 MGI PMID:10101115 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0020301 short tongue IAGP N RGD:5509061 20221027 MGI PMID:10049363 736734 Pitx1 paired-like homeodomain transcription factor 1 gene MP:0030859 absent sesamoid bone of gastrocnemius IAGP N RGD:5509061 20181025 MGI PMID:10101115 736737 Aanat arylalkylamine N-acetyltransferase gene MP:0011728 abnormal pineal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:3620949 736737 Aanat arylalkylamine N-acetyltransferase gene MP:0011729 abnormal pineal gland melatonin secretion IAGP N RGD:5509061 20141003 MGI PMID:3620949 736741 Prdm4 PR domain containing 4 gene MP:0000690 absent spleen IEA N RGD:5509061 20181227 MGI 736741 Prdm4 PR domain containing 4 gene MP:0001297 microphthalmia IEA N RGD:5509061 20181227 MGI 736741 Prdm4 PR domain containing 4 gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201022 MGI 736741 Prdm4 PR domain containing 4 gene MP:0001322 abnormal iris morphology IEA N RGD:5509061 20201231 MGI 736741 Prdm4 PR domain containing 4 gene MP:0001406 abnormal gait IEA N RGD:5509061 20160421 MGI 736741 Prdm4 PR domain containing 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918801 736741 Prdm4 PR domain containing 4 gene MP:0002764 short tibia IEA N RGD:5509061 20230601 MGI 736741 Prdm4 PR domain containing 4 gene MP:0002953 thick ventricular wall IEA N RGD:5509061 20211021 MGI 736741 Prdm4 PR domain containing 4 gene MP:0003921 abnormal heart left ventricle morphology IEA N RGD:5509061 20160421 MGI 736741 Prdm4 PR domain containing 4 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20160421 MGI 736741 Prdm4 PR domain containing 4 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 736741 Prdm4 PR domain containing 4 gene MP:0005599 increased cardiac muscle contractility IEA N RGD:5509061 20210128 MGI 736741 Prdm4 PR domain containing 4 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 736741 Prdm4 PR domain containing 4 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20160421 MGI 736741 Prdm4 PR domain containing 4 gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20181227 MGI 736743 Slit1 slit guidance ligand 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20211021 MGI 736743 Slit1 slit guidance ligand 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15084255 736743 Slit1 slit guidance ligand 1 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:15091338 736743 Slit1 slit guidance ligand 1 gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:18054781 736743 Slit1 slit guidance ligand 1 gene MP:0005237 abnormal olfactory tract morphology IAGP N RGD:5509061 20141003 MGI PMID:17360927 736743 Slit1 slit guidance ligand 1 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:18054781 736743 Slit1 slit guidance ligand 1 gene MP:0009678 abnormal spinal cord lateral column morphology IAGP N RGD:5509061 20141003 MGI PMID:15091338 736743 Slit1 slit guidance ligand 1 gene MP:0009695 abnormal spinal cord ventral commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:15091338 736743 Slit1 slit guidance ligand 1 gene MP:0009944 abnormal olfactory lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:17360927 736743 Slit1 slit guidance ligand 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18054781 736745 Lsr lipolysis stimulated lipoprotein receptor gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15265030 736745 Lsr lipolysis stimulated lipoprotein receptor gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:15265030 736745 Lsr lipolysis stimulated lipoprotein receptor gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15265030 736745 Lsr lipolysis stimulated lipoprotein receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15265030 736745 Lsr lipolysis stimulated lipoprotein receptor gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:15265030 736745 Lsr lipolysis stimulated lipoprotein receptor gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:15265030 736745 Lsr lipolysis stimulated lipoprotein receptor gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15265030 736748 Tenm2 teneurin transmembrane protein 2 gene MP:0000805 abnormal visual cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:23884953 736748 Tenm2 teneurin transmembrane protein 2 gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20141003 MGI PMID:23884953 736748 Tenm2 teneurin transmembrane protein 2 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:23884953 736748 Tenm2 teneurin transmembrane protein 2 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:23884953 736748 Tenm2 teneurin transmembrane protein 2 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:23884953 736748 Tenm2 teneurin transmembrane protein 2 gene MP:0004165 abnormal lateral geniculate nucleus morphology IAGP N RGD:5509061 20141003 MGI PMID:23884953 736748 Tenm2 teneurin transmembrane protein 2 gene MP:0005241 abnormal retina ganglion layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23884953 736748 Tenm2 teneurin transmembrane protein 2 gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20141003 MGI PMID:23884953 736751 Aqp11 aquaporin 11 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 736751 Aqp11 aquaporin 11 gene MP:0000521 abnormal kidney cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:18701606 736751 Aqp11 aquaporin 11 gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:16107722 736751 Aqp11 aquaporin 11 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:23275615 736751 Aqp11 aquaporin 11 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18701606 736751 Aqp11 aquaporin 11 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23275615 736751 Aqp11 aquaporin 11 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16107722 736751 Aqp11 aquaporin 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16107722 736751 Aqp11 aquaporin 11 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18701606 736751 Aqp11 aquaporin 11 gene MP:0002546 mydriasis IEA N RGD:5509061 20240627 MGI 736751 Aqp11 aquaporin 11 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23275615 736751 Aqp11 aquaporin 11 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23275615 736751 Aqp11 aquaporin 11 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18701606 736751 Aqp11 aquaporin 11 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:18701606 736751 Aqp11 aquaporin 11 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:16107722 736751 Aqp11 aquaporin 11 gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:23275615 736751 Aqp11 aquaporin 11 gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:23275615 736751 Aqp11 aquaporin 11 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:16107722 736751 Aqp11 aquaporin 11 gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:18701606 736751 Aqp11 aquaporin 11 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:16107722 736751 Aqp11 aquaporin 11 gene MP:0004756 abnormal proximal convoluted tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18701606 736751 Aqp11 aquaporin 11 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:16107722 736751 Aqp11 aquaporin 11 gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:18701606 736751 Aqp11 aquaporin 11 gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:23275615 736751 Aqp11 aquaporin 11 gene MP:0005553 increased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:18701606 736751 Aqp11 aquaporin 11 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:16107722 736751 Aqp11 aquaporin 11 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:18701606 736751 Aqp11 aquaporin 11 gene MP:0005566 decreased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23275615 736751 Aqp11 aquaporin 11 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:23275615 736751 Aqp11 aquaporin 11 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18701606 736751 Aqp11 aquaporin 11 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10224267 736751 Aqp11 aquaporin 11 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18701606 736751 Aqp11 aquaporin 11 gene MP:0011352 proximal convoluted tubule brush border loss IAGP N RGD:5509061 20141003 MGI PMID:18701606 736751 Aqp11 aquaporin 11 gene MP:0011436 decreased urine magnesium level IEA N RGD:5509061 20200402 MGI 736753 Stmn4 stathmin-like 4 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 736753 Stmn4 stathmin-like 4 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:15956281 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:16283625 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:21907140 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000899 abnormal corpora quadrigemina morphology IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000904 abnormal superior colliculus morphology IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:16283625 736754 Ireb2 iron responsive element binding protein 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:23135277 736754 Ireb2 iron responsive element binding protein 2 gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16283625 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15956281 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16283625 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:15956281 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:21907140 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:15956281 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:16283625 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:21907140 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:15956281 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:16283625 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:21907140 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16283625 736754 Ireb2 iron responsive element binding protein 2 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:16283625 736754 Ireb2 iron responsive element binding protein 2 gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0004147 increased porphyrin level IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0004742 abnormal vestibular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:21907140 736754 Ireb2 iron responsive element binding protein 2 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:14726953 736754 Ireb2 iron responsive element binding protein 2 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15956281 736754 Ireb2 iron responsive element binding protein 2 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16283625 736754 Ireb2 iron responsive element binding protein 2 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:21907140 736754 Ireb2 iron responsive element binding protein 2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0005654 porphyria IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:21907140 736754 Ireb2 iron responsive element binding protein 2 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:15956281 736754 Ireb2 iron responsive element binding protein 2 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:16283625 736754 Ireb2 iron responsive element binding protein 2 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:21907140 736754 Ireb2 iron responsive element binding protein 2 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:15956281 736754 Ireb2 iron responsive element binding protein 2 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:16283625 736754 Ireb2 iron responsive element binding protein 2 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:21907140 736754 Ireb2 iron responsive element binding protein 2 gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:21907140 736754 Ireb2 iron responsive element binding protein 2 gene MP:0008935 decreased mean platelet volume IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0009940 abnormal hippocampus pyramidal cell morphology IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0009978 abnormal cerebellum white matter morphology IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0010375 increased kidney iron level IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20141003 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0011890 increased circulating ferritin level IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0011897 decreased circulating unsaturated transferrin level IAGP N RGD:5509061 20141003 MGI PMID:21907140 736754 Ireb2 iron responsive element binding protein 2 gene MP:0020338 abnormal hippocampal pyramidal neuron dendrite morphology IAGP N RGD:5509061 20161013 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0020365 increased brain iron level IAGP N RGD:5509061 20161020 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0020365 increased brain iron level IAGP N RGD:5509061 20161020 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0020366 decreased brain iron level IAGP N RGD:5509061 20161020 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0020368 decreased heart iron level IAGP N RGD:5509061 20161020 MGI PMID:24896637 736754 Ireb2 iron responsive element binding protein 2 gene MP:0020369 increased intestinal iron level IAGP N RGD:5509061 20161020 MGI PMID:11175792 736754 Ireb2 iron responsive element binding protein 2 gene MP:0020369 increased intestinal iron level IAGP N RGD:5509061 20161020 MGI PMID:15956281 736754 Ireb2 iron responsive element binding protein 2 gene MP:0020369 increased intestinal iron level IAGP N RGD:5509061 20161020 MGI PMID:16283625 736754 Ireb2 iron responsive element binding protein 2 gene MP:0020369 increased intestinal iron level IAGP N RGD:5509061 20161020 MGI PMID:24896637 736758 Drgx dorsal root ganglia homeobox gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0000639 abnormal adrenal gland morphology IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11498051 736758 Drgx dorsal root ganglia homeobox gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:11498051 736758 Drgx dorsal root ganglia homeobox gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0001148 enlarged testis IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11498051 736758 Drgx dorsal root ganglia homeobox gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:11498051 736758 Drgx dorsal root ganglia homeobox gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11498051 736758 Drgx dorsal root ganglia homeobox gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11498051 736758 Drgx dorsal root ganglia homeobox gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:11498051 736758 Drgx dorsal root ganglia homeobox gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0002989 small kidney IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11498051 736758 Drgx dorsal root ganglia homeobox gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:11498051 736758 Drgx dorsal root ganglia homeobox gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11498051 736758 Drgx dorsal root ganglia homeobox gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 736758 Drgx dorsal root ganglia homeobox gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 736760 Dgkz diacylglycerol kinase zeta gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:12883552 736760 Dgkz diacylglycerol kinase zeta gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20200910 MGI PMID:31801815 736760 Dgkz diacylglycerol kinase zeta gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:17028587 736760 Dgkz diacylglycerol kinase zeta gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12883552 736760 Dgkz diacylglycerol kinase zeta gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20200910 MGI PMID:31801815 736760 Dgkz diacylglycerol kinase zeta gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20200910 MGI PMID:31801815 736760 Dgkz diacylglycerol kinase zeta gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20200910 MGI PMID:31801815 736760 Dgkz diacylglycerol kinase zeta gene MP:0003850 abnormal thymocyte activation IAGP N RGD:5509061 20141003 MGI PMID:17028587 736760 Dgkz diacylglycerol kinase zeta gene MP:0005004 abnormal lymphocyte anergy IAGP N RGD:5509061 20141003 MGI PMID:17028587 736760 Dgkz diacylglycerol kinase zeta gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:12883552 736760 Dgkz diacylglycerol kinase zeta gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17028587 736760 Dgkz diacylglycerol kinase zeta gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12883552 736760 Dgkz diacylglycerol kinase zeta gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12883552 736760 Dgkz diacylglycerol kinase zeta gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:12883552 736760 Dgkz diacylglycerol kinase zeta gene MP:0008686 abnormal interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17028587 736760 Dgkz diacylglycerol kinase zeta gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20200910 MGI PMID:31801815 736760 Dgkz diacylglycerol kinase zeta gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20200910 MGI PMID:31801815 736760 Dgkz diacylglycerol kinase zeta gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:12883552 736760 Dgkz diacylglycerol kinase zeta gene MP:0011891 decreased circulating ferritin level IAGP N RGD:5509061 20200910 MGI PMID:31801815 736760 Dgkz diacylglycerol kinase zeta gene MP:0020914 decreased susceptibility to Riboviria infection IAGP N RGD:5509061 20200430 MGI PMID:12883552 736761 Atf2 activating transcription factor 2 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200514 MGI 736761 Atf2 activating transcription factor 2 gene MP:0000274 enlarged heart IEA N RGD:5509061 20200514 MGI 736761 Atf2 activating transcription factor 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17699753 736761 Atf2 activating transcription factor 2 gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20200514 MGI 736761 Atf2 activating transcription factor 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:17699753 736761 Atf2 activating transcription factor 2 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17699753 736761 Atf2 activating transcription factor 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20200514 MGI 736761 Atf2 activating transcription factor 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0000885 ectopic Purkinje cell IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200514 MGI 736761 Atf2 activating transcription factor 2 gene MP:0001147 small testis IEA N RGD:5509061 20200514 MGI 736761 Atf2 activating transcription factor 2 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:10364225 736761 Atf2 activating transcription factor 2 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:18227516 736761 Atf2 activating transcription factor 2 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18227516 736761 Atf2 activating transcription factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11157857 736761 Atf2 activating transcription factor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:10694580 736761 Atf2 activating transcription factor 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:10364225 736761 Atf2 activating transcription factor 2 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:17699753 736761 Atf2 activating transcription factor 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:17699753 736761 Atf2 activating transcription factor 2 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:10364225 736761 Atf2 activating transcription factor 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17699753 736761 Atf2 activating transcription factor 2 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19948881 736761 Atf2 activating transcription factor 2 gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:10364225 736761 Atf2 activating transcription factor 2 gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:18227516 736761 Atf2 activating transcription factor 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20200514 MGI 736761 Atf2 activating transcription factor 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 736761 Atf2 activating transcription factor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18227516 736761 Atf2 activating transcription factor 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0002730 head shaking IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17699753 736761 Atf2 activating transcription factor 2 gene MP:0002856 abnormal vestibular ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19948881 736761 Atf2 activating transcription factor 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11157857 736761 Atf2 activating transcription factor 2 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210128 MGI 736761 Atf2 activating transcription factor 2 gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0003144 decreased otolith number IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0003231 abnormal placenta vasculature IAGP N RGD:5509061 20141003 MGI PMID:10364225 736761 Atf2 activating transcription factor 2 gene MP:0003410 abnormal artery development IAGP N RGD:5509061 20141003 MGI PMID:17717295 736761 Atf2 activating transcription factor 2 gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17699753 736761 Atf2 activating transcription factor 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17699753 736761 Atf2 activating transcription factor 2 gene MP:0004328 decreased vestibular hair cell number IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0004330 abnormal vestibular saccular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0004333 abnormal utricular macula morphology IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0004517 decreased vestibular hair cell stereocilia number IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:10364225 736761 Atf2 activating transcription factor 2 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:19948881 736761 Atf2 activating transcription factor 2 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:17699753 736761 Atf2 activating transcription factor 2 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19948881 736761 Atf2 activating transcription factor 2 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19948881 736761 Atf2 activating transcription factor 2 gene MP:0005307 head tossing IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20220519 MGI 736761 Atf2 activating transcription factor 2 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17699753 736761 Atf2 activating transcription factor 2 gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0006397 disorganized long bone epiphyseal plate IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17699753 736761 Atf2 activating transcription factor 2 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:10694580 736761 Atf2 activating transcription factor 2 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:10694580 736761 Atf2 activating transcription factor 2 gene MP:0008578 decreased circulating interferon-gamma level IAGP N RGD:5509061 20141003 MGI PMID:10694580 736761 Atf2 activating transcription factor 2 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:11157857 736761 Atf2 activating transcription factor 2 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19948881 736761 Atf2 activating transcription factor 2 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20211021 MGI 736761 Atf2 activating transcription factor 2 gene MP:0008974 proportional dwarf IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0009133 decreased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19948881 736761 Atf2 activating transcription factor 2 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10694580 736761 Atf2 activating transcription factor 2 gene MP:0011044 increased lung elastance IEA N RGD:5509061 20231207 MGI 736761 Atf2 activating transcription factor 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10364225 736761 Atf2 activating transcription factor 2 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17699753 736761 Atf2 activating transcription factor 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17699753 736761 Atf2 activating transcription factor 2 gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 736761 Atf2 activating transcription factor 2 gene MP:0014288 rhizomelic limb IAGP N RGD:5509061 20230824 MGI PMID:8538792 736761 Atf2 activating transcription factor 2 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20221215 MGI 736761 Atf2 activating transcription factor 2 gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:11157857 736761 Atf2 activating transcription factor 2 gene MP:0020937 increased susceptibility to Picornaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:11157857 736763 Sncb synuclein, beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16269331 736763 Sncb synuclein, beta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16269331 736763 Sncb synuclein, beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15465911 736763 Sncb synuclein, beta gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:16269331 736763 Sncb synuclein, beta gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20201231 MGI 736763 Sncb synuclein, beta gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:15465911 736763 Sncb synuclein, beta gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20220519 MGI 736763 Sncb synuclein, beta gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:15465911 736763 Sncb synuclein, beta gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20170105 MGI 736764 Kcnip1 Kv channel-interacting protein 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20160128 MGI PMID:19352544 736764 Kcnip1 Kv channel-interacting protein 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 736764 Kcnip1 Kv channel-interacting protein 1 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20160128 MGI PMID:19352544 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:12655058 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:12702666 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:4970465 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001293 anophthalmia IEA N RGD:5509061 20220519 MGI 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:4970465 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001299 abnormal eye distance/ position IAGP N RGD:5509061 20141003 MGI PMID:4970465 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001307 fused cornea and lens IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:4970465 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001328 disorganized retina layers IAGP N RGD:5509061 20220331 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:15728853 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20220428 MGI 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12702666 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:15728853 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20210826 MGI 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001566 increased circulating phosphate level IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:4970465 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20230810 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:17540357 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0002327 abnormal respiratory function IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0002626 increased heart rate IEA N RGD:5509061 20210128 MGI 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20240523 MGI 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0002738 hyperresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:15728853 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0002804 abnormal motor learning IEA N RGD:5509061 20210826 MGI 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:4970465 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0003063 increased coping response IEA N RGD:5509061 20160421 MGI 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15950611 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0003224 neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:12829322 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:15950611 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:17540357 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0003998 decreased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0004102 abnormal dorsal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:12829322 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0005102 abnormal iris pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4970465 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0005176 eyelids fail to open IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0005193 abnormal anterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:4970465 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0005195 abnormal posterior eye segment morphology IAGP N RGD:5509061 20141003 MGI PMID:4970465 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0005545 abnormal lens development IAGP N RGD:5509061 20141003 MGI PMID:4970465 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20240523 MGI 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0005573 increased pulmonary respiratory rate IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0005586 decreased tidal volume IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:12829322 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0008493 alpha-synuclein inclusion body IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0008532 decreased chemical nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0008805 decreased circulating amylase level IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0008822 decreased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0008918 microgliosis IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:15950611 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0010052 increased grip strength IEA N RGD:5509061 20170105 MGI 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20141003 MGI PMID:22764233 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0010571 shortened ST segment IEA N RGD:5509061 20160421 MGI 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20160421 MGI 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0011448 decreased dopaminergic neuron number IAGP N RGD:5509061 20141003 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0011962 increased cornea thickness IAGP N RGD:5509061 20230810 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0012101 acoria IAGP N RGD:5509061 20141003 MGI PMID:4970465 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0013219 abnormal substantia nigra pars compacta morphology IAGP N RGD:5509061 20141003 MGI PMID:12829322 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20181227 MGI 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0013453 enlarged lacrimal gland IAGP N RGD:5509061 20150205 MGI PMID:4970465 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0020543 decreased substantia nigra size IAGP N RGD:5509061 20180301 MGI PMID:12655058 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:20033184 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0021107 retina fold IAGP N RGD:5509061 20220331 MGI PMID:4970465 736766 Pitx3 paired-like homeodomain transcription factor 3 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:15728853 736768 Slc12a4 solute carrier family 12, member 4 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20170518 MGI PMID:26450986 736768 Slc12a4 solute carrier family 12, member 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20170518 MGI PMID:26450986 736768 Slc12a4 solute carrier family 12, member 4 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20170518 MGI PMID:26450986 736768 Slc12a4 solute carrier family 12, member 4 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20170518 MGI PMID:26450986 736768 Slc12a4 solute carrier family 12, member 4 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20170518 MGI PMID:26450986 736768 Slc12a4 solute carrier family 12, member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20170518 MGI PMID:26450986 736768 Slc12a4 solute carrier family 12, member 4 gene MP:0002295 abnormal pulmonary circulation IAGP N RGD:5509061 20170518 MGI PMID:26450986 736768 Slc12a4 solute carrier family 12, member 4 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20170518 MGI PMID:26450986 736768 Slc12a4 solute carrier family 12, member 4 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20170518 MGI PMID:26450986 736768 Slc12a4 solute carrier family 12, member 4 gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20170518 MGI PMID:26450986 736768 Slc12a4 solute carrier family 12, member 4 gene MP:0002813 microcytosis IAGP N RGD:5509061 20170518 MGI PMID:26450986 736768 Slc12a4 solute carrier family 12, member 4 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20170518 MGI PMID:26450986 736768 Slc12a4 solute carrier family 12, member 4 gene MP:0008387 hypochromic anemia IAGP N RGD:5509061 20170518 MGI PMID:26450986 736768 Slc12a4 solute carrier family 12, member 4 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20170518 MGI PMID:26450986 736768 Slc12a4 solute carrier family 12, member 4 gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20170518 MGI PMID:26450986 736770 Gpr26 G protein-coupled receptor 26 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21924326 736770 Gpr26 G protein-coupled receptor 26 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22815809 736770 Gpr26 G protein-coupled receptor 26 gene MP:0001987 alcohol preference IAGP N RGD:5509061 20141003 MGI PMID:21924326 736770 Gpr26 G protein-coupled receptor 26 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22815809 736770 Gpr26 G protein-coupled receptor 26 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22815809 736770 Gpr26 G protein-coupled receptor 26 gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:21924326 736770 Gpr26 G protein-coupled receptor 26 gene MP:0002797 increased thigmotaxis IAGP N RGD:5509061 20141003 MGI PMID:21924326 736770 Gpr26 G protein-coupled receptor 26 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:22815809 736770 Gpr26 G protein-coupled receptor 26 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22815809 736770 Gpr26 G protein-coupled receptor 26 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22815809 736770 Gpr26 G protein-coupled receptor 26 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:22815809 736770 Gpr26 G protein-coupled receptor 26 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22815809 736770 Gpr26 G protein-coupled receptor 26 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22815809 736770 Gpr26 G protein-coupled receptor 26 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22815809 736770 Gpr26 G protein-coupled receptor 26 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:22815809 736770 Gpr26 G protein-coupled receptor 26 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:22815809 736770 Gpr26 G protein-coupled receptor 26 gene MP:0011613 decreased circulating ghrelin level IAGP N RGD:5509061 20141003 MGI PMID:22815809 736770 Gpr26 G protein-coupled receptor 26 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:22815809 736771 Pld2 phospholipase D2 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:21147981 736771 Pld2 phospholipase D2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23109426 736771 Pld2 phospholipase D2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:22974101 736771 Pld2 phospholipase D2 gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:21610093 736771 Pld2 phospholipase D2 gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:21147981 736771 Pld2 phospholipase D2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20170413 MGI PMID:22974101 736771 Pld2 phospholipase D2 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20170413 MGI PMID:22974101 736771 Pld2 phospholipase D2 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20170413 MGI PMID:22974101 736771 Pld2 phospholipase D2 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20170413 MGI PMID:22974101 736771 Pld2 phospholipase D2 gene MP:0009453 enhanced contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:21147981 736771 Pld2 phospholipase D2 gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:21147981 736771 Pld2 phospholipase D2 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:22974101 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:17273169 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17273169 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141003 MGI PMID:17273169 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19917889 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21493890 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:17273169 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0003393 decreased cardiac output IAGP N RGD:5509061 20141003 MGI PMID:17273169 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20170601 MGI PMID:25910799 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0003820 increased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:19917889 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17273169 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19917889 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21493890 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17273169 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19917889 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0004878 increased systemic vascular resistance IAGP N RGD:5509061 20141003 MGI PMID:19917889 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:17273169 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:19917889 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:21493890 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20170601 MGI PMID:25910799 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:19917889 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20141003 MGI PMID:21493890 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0005332 abnormal amino acid level IAGP N RGD:5509061 20170601 MGI PMID:25910799 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17273169 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:21493890 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19917889 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20170601 MGI PMID:25910799 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19917889 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17273169 736772 Ddah1 dimethylarginine dimethylaminohydrolase 1 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19757398 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:9180080 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:16753145 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0000947 convulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:9180080 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:24280215 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9180080 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:24280215 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0002064 seizures IAGP N RGD:5509061 20160609 MGI PMID:25834045 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16753145 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:24280215 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9180080 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20160609 MGI PMID:25834045 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24280215 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:9180080 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20160609 MGI PMID:25834045 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16753145 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:9180080 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:24280215 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20160609 MGI PMID:25834045 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:24280215 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0010014 hippocampus pyramidal cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12904478 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17607354 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0011854 cerebral edema IAGP N RGD:5509061 20141003 MGI PMID:9180080 736773 Slc1a2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene MP:0021009 abnormal synaptic physiology IAGP N RGD:5509061 20210805 MGI PMID:25834045 736775 Lif leukemia inhibitory factor gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0000382 underdeveloped hair follicles IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0000734 muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:15597051 736775 Lif leukemia inhibitory factor gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:15597051 736775 Lif leukemia inhibitory factor gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9740023 736775 Lif leukemia inhibitory factor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:1522892 736775 Lif leukemia inhibitory factor gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:15576827 736775 Lif leukemia inhibitory factor gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0001179 thick pulmonary interalveolar septum IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:14741342 736775 Lif leukemia inhibitory factor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:1522892 736775 Lif leukemia inhibitory factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8497320 736775 Lif leukemia inhibitory factor gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:9651226 736775 Lif leukemia inhibitory factor gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:18548006 736775 Lif leukemia inhibitory factor gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:18521186 736775 Lif leukemia inhibitory factor gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:10935540 736775 Lif leukemia inhibitory factor gene MP:0001728 failure of embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:1522892 736775 Lif leukemia inhibitory factor gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:1522892 736775 Lif leukemia inhibitory factor gene MP:0001881 abnormal mammary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:12810593 736775 Lif leukemia inhibitory factor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10935540 736775 Lif leukemia inhibitory factor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:1522892 736775 Lif leukemia inhibitory factor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8497320 736775 Lif leukemia inhibitory factor gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18521186 736775 Lif leukemia inhibitory factor gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0002446 abnormal macrophage morphology IAGP N RGD:5509061 20141003 MGI PMID:15576827 736775 Lif leukemia inhibitory factor gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:14741342 736775 Lif leukemia inhibitory factor gene MP:0002655 abnormal keratinocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0002664 decreased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:8770940 736775 Lif leukemia inhibitory factor gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18521186 736775 Lif leukemia inhibitory factor gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10712626 736775 Lif leukemia inhibitory factor gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:19906980 736775 Lif leukemia inhibitory factor gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:18521186 736775 Lif leukemia inhibitory factor gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0004702 increased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:14741342 736775 Lif leukemia inhibitory factor gene MP:0004810 decreased hematopoietic stem cell number IAGP N RGD:5509061 20141003 MGI PMID:8497320 736775 Lif leukemia inhibitory factor gene MP:0004950 abnormal brain vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18521186 736775 Lif leukemia inhibitory factor gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:18548006 736775 Lif leukemia inhibitory factor gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:18548006 736775 Lif leukemia inhibitory factor gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:18548006 736775 Lif leukemia inhibitory factor gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:15576827 736775 Lif leukemia inhibitory factor gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:18548006 736775 Lif leukemia inhibitory factor gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:9651226 736775 Lif leukemia inhibitory factor gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8497320 736775 Lif leukemia inhibitory factor gene MP:0005137 increased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:14741342 736775 Lif leukemia inhibitory factor gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:19906980 736775 Lif leukemia inhibitory factor gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:10712626 736775 Lif leukemia inhibitory factor gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:18521186 736775 Lif leukemia inhibitory factor gene MP:0005343 increased circulating aspartate transaminase level IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:14741342 736775 Lif leukemia inhibitory factor gene MP:0006086 decreased body mass index IAGP N RGD:5509061 20141003 MGI PMID:14741342 736775 Lif leukemia inhibitory factor gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:12810593 736775 Lif leukemia inhibitory factor gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:12810593 736775 Lif leukemia inhibitory factor gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:18548006 736775 Lif leukemia inhibitory factor gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:14741342 736775 Lif leukemia inhibitory factor gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0008641 increased circulating interleukin-1 beta level IAGP N RGD:5509061 20141003 MGI PMID:9651226 736775 Lif leukemia inhibitory factor gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:8497320 736775 Lif leukemia inhibitory factor gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:8497320 736775 Lif leukemia inhibitory factor gene MP:0009117 abnormal white fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14741342 736775 Lif leukemia inhibitory factor gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:14741342 736775 Lif leukemia inhibitory factor gene MP:0009394 increased uterine NK cell number IAGP N RGD:5509061 20141003 MGI PMID:15576827 736775 Lif leukemia inhibitory factor gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20141003 MGI PMID:12810593 736775 Lif leukemia inhibitory factor gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:12810593 736775 Lif leukemia inhibitory factor gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:18521186 736775 Lif leukemia inhibitory factor gene MP:0009662 abnormal uterine receptivity IAGP N RGD:5509061 20141003 MGI PMID:10935540 736775 Lif leukemia inhibitory factor gene MP:0009665 abnormal embryo apposition IAGP N RGD:5509061 20141003 MGI PMID:10935540 736775 Lif leukemia inhibitory factor gene MP:0009666 abnormal embryo attachment IAGP N RGD:5509061 20141003 MGI PMID:10935540 736775 Lif leukemia inhibitory factor gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0009946 abnormal olfactory bulb layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0009947 abnormal olfactory bulb external plexiform layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0009951 abnormal olfactory bulb mitral cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0009954 abnormal mitral cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:15702085 736775 Lif leukemia inhibitory factor gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0010817 absent type I pneumocytes IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:18548006 736775 Lif leukemia inhibitory factor gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12591604 736775 Lif leukemia inhibitory factor gene MP:0014273 abnormal skin vasculature morphology IAGP N RGD:5509061 20230810 MGI PMID:18521186 736775 Lif leukemia inhibitory factor gene MP:0020161 increased vascular endothelial cell proliferation IAGP N RGD:5509061 20160616 MGI PMID:18521186 736775 Lif leukemia inhibitory factor gene MP:0031234 increased circulating serum amyloid protein level IAGP N RGD:5509061 20210225 MGI PMID:15702085 736776 Mag myelin-associated glycoprotein gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20211021 MGI 736776 Mag myelin-associated glycoprotein gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:7516497 736776 Mag myelin-associated glycoprotein gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:7519026 736776 Mag myelin-associated glycoprotein gene MP:0000920 abnormal myelination IAGP N RGD:5509061 20141003 MGI PMID:9482783 736776 Mag myelin-associated glycoprotein gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:7539694 736776 Mag myelin-associated glycoprotein gene MP:0000947 convulsive seizures IEA N RGD:5509061 20170105 MGI 736776 Mag myelin-associated glycoprotein gene MP:0000953 abnormal oligodendrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:9034827 736776 Mag myelin-associated glycoprotein gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7539694 736776 Mag myelin-associated glycoprotein gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:7516497 736776 Mag myelin-associated glycoprotein gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:7516497 736776 Mag myelin-associated glycoprotein gene MP:0001406 abnormal gait IAGP N RGD:5509061 20160929 MGI PMID:27534441 736776 Mag myelin-associated glycoprotein gene MP:0001440 abnormal grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:7516497 736776 Mag myelin-associated glycoprotein gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20150305 MGI PMID:23118208 736776 Mag myelin-associated glycoprotein gene MP:0003064 decreased coping response IEA N RGD:5509061 20210128 MGI 736776 Mag myelin-associated glycoprotein gene MP:0003863 decreased aggression towards mice IAGP N RGD:5509061 20150305 MGI PMID:23118208 736776 Mag myelin-associated glycoprotein gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:7519026 736776 Mag myelin-associated glycoprotein gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:9011400 736776 Mag myelin-associated glycoprotein gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 736776 Mag myelin-associated glycoprotein gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20150305 MGI PMID:23118208 736776 Mag myelin-associated glycoprotein gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:7516497 736776 Mag myelin-associated glycoprotein gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:7519026 736776 Mag myelin-associated glycoprotein gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:7539694 736776 Mag myelin-associated glycoprotein gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:9011400 736776 Mag myelin-associated glycoprotein gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:9034827 736776 Mag myelin-associated glycoprotein gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20210401 MGI PMID:32908139 736776 Mag myelin-associated glycoprotein gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:7539694 736776 Mag myelin-associated glycoprotein gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:9011400 736776 Mag myelin-associated glycoprotein gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20150305 MGI PMID:23118208 736776 Mag myelin-associated glycoprotein gene MP:0010052 increased grip strength IEA N RGD:5509061 20240523 MGI 736776 Mag myelin-associated glycoprotein gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20160421 MGI 736776 Mag myelin-associated glycoprotein gene MP:0012674 tomacula IAGP N RGD:5509061 20170629 MGI PMID:27504968 736776 Mag myelin-associated glycoprotein gene MP:0013438 dysmyelination IAGP N RGD:5509061 20170629 MGI PMID:27504968 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19321764 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:9185557 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19321764 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0001469 abnormal contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:9185557 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12559117 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:9185557 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:18093519 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20141003 MGI 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20141003 MGI 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20190711 MGI PMID:30401923 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0002556 abnormal cocaine consumption IAGP N RGD:5509061 20141003 MGI PMID:11528416 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:22561452 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20141003 MGI 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20141003 MGI 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:9185557 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16280580 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0003477 abnormal nerve fiber response IAGP N RGD:5509061 20141003 MGI PMID:18093519 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:19587272 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:18093519 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0006299 abnormal latent inhibition of conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19321764 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:11528416 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20141003 MGI 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0012296 impaired discrimination learning IAGP N RGD:5509061 20190711 MGI PMID:30401923 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0012315 impaired learning IAGP N RGD:5509061 20190711 MGI PMID:30401923 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0014115 cognitive inflexibility IAGP N RGD:5509061 20190711 MGI PMID:30401923 736778 Grm5 glutamate receptor, metabotropic 5 gene MP:0020340 abnormal inhibitory learning IAGP N RGD:5509061 20160915 MGI PMID:19321764 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0000180 abnormal circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12668679 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12668679 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11773510 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:12668679 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12668679 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:12482759 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:12668679 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0001265 decreased body size IEA N RGD:5509061 20111116 MGI 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0001523 impaired righting response IEA N RGD:5509061 20111116 MGI 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0001524 impaired limb coordination IEA N RGD:5509061 20111116 MGI 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:12668679 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0002083 premature death IEA N RGD:5509061 20111116 MGI 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12668679 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20150326 MGI PMID:21292027 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0003312 abnormal locomotor coordination IEA N RGD:5509061 20111116 MGI 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12668679 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0008025 brain vacuoles IEA N RGD:5509061 20111116 MGI 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0010155 abnormal intestine physiology IAGP N RGD:5509061 20150326 MGI PMID:21292027 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0011086 postnatal lethality, incomplete penetrance IEA N RGD:5509061 20111116 MGI 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0012334 decreased circulating homocysteine level IAGP N RGD:5509061 20180920 MGI PMID:12482759 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0012338 decreased bile salt level IAGP N RGD:5509061 20150326 MGI PMID:21292027 736786 Pemt phosphatidylethanolamine N-methyltransferase gene MP:0014478 increased feces bile salt level IAGP N RGD:5509061 20240704 MGI PMID:21292027 736789 Col5a2 collagen, type V, alpha 2 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20170202 MGI PMID:25987251 736789 Col5a2 collagen, type V, alpha 2 gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0001244 thin dermal layer IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0001312 abnormal cornea morphology IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20170202 MGI PMID:25987251 736789 Col5a2 collagen, type V, alpha 2 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170202 MGI PMID:25987251 736789 Col5a2 collagen, type V, alpha 2 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0003089 decreased skin tensile strength IAGP N RGD:5509061 20170202 MGI PMID:25987251 736789 Col5a2 collagen, type V, alpha 2 gene MP:0003092 decreased cornea stroma thickness IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0003705 abnormal hypodermis morphology IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0003717 pallor IAGP N RGD:5509061 20170202 MGI PMID:25987251 736789 Col5a2 collagen, type V, alpha 2 gene MP:0004127 thick hypodermis IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20170202 MGI PMID:25987251 736789 Col5a2 collagen, type V, alpha 2 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20170202 MGI PMID:25987251 736789 Col5a2 collagen, type V, alpha 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7704020 736789 Col5a2 collagen, type V, alpha 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20170202 MGI PMID:25987251 736789 Col5a2 collagen, type V, alpha 2 gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:7704020 736799 Tfpi2 tissue factor pathway inhibitor 2 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 736799 Tfpi2 tissue factor pathway inhibitor 2 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20210805 MGI PMID:30254643 736799 Tfpi2 tissue factor pathway inhibitor 2 gene MP:0008593 increased circulating interleukin-10 level IAGP N RGD:5509061 20210805 MGI PMID:30254643 736799 Tfpi2 tissue factor pathway inhibitor 2 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20210805 MGI PMID:30254643 736799 Tfpi2 tissue factor pathway inhibitor 2 gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20210805 MGI PMID:30254643 736799 Tfpi2 tissue factor pathway inhibitor 2 gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20210805 MGI PMID:30254643 736802 Cartpt CART prepropeptide gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 736802 Cartpt CART prepropeptide gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210520 MGI 736802 Cartpt CART prepropeptide gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:15927717 736802 Cartpt CART prepropeptide gene MP:0001304 cataract IEA N RGD:5509061 20231207 MGI 736802 Cartpt CART prepropeptide gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 736802 Cartpt CART prepropeptide gene MP:0001488 increased startle reflex IEA N RGD:5509061 20211021 MGI 736802 Cartpt CART prepropeptide gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15927717 736802 Cartpt CART prepropeptide gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210520 MGI 736802 Cartpt CART prepropeptide gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 736802 Cartpt CART prepropeptide gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20231207 MGI 736802 Cartpt CART prepropeptide gene MP:0002989 small kidney IEA N RGD:5509061 20210520 MGI 736802 Cartpt CART prepropeptide gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15927717 736802 Cartpt CART prepropeptide gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:15724149 736802 Cartpt CART prepropeptide gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:15724149 736802 Cartpt CART prepropeptide gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:15724149 736802 Cartpt CART prepropeptide gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15927717 736802 Cartpt CART prepropeptide gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:11564703 736802 Cartpt CART prepropeptide gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:11564703 736802 Cartpt CART prepropeptide gene MP:0009453 enhanced contextual conditioning behavior IEA N RGD:5509061 20210128 MGI 736802 Cartpt CART prepropeptide gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11564703 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0000220 increased monocyte cell number IEA N RGD:5509061 20231207 MGI 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0000494 abnormal cecum morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0001491 unresponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0001513 limb grasping IEA N RGD:5509061 20231207 MGI 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0001664 abnormal digestion IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111215 MGI 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0002608 increased hematocrit IEA N RGD:5509061 20231207 MGI 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0003131 increased erythrocyte cell number IEA N RGD:5509061 20231207 MGI 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0004841 abnormal small intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0005036 diarrhea IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0008074 increased CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0008108 abnormal small intestinal villus morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0008561 decreased tumor necrosis factor secretion IEA N RGD:5509061 20181011 MGI 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0008657 increased interleukin-1 beta secretion IEA N RGD:5509061 20181011 MGI 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0009511 distended stomach IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0010792 abnormal stomach mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:22896614 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0010841 increased central memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0011081 decreased macrophage apoptosis IEA N RGD:5509061 20181011 MGI 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23229899 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20240704 MGI PMID:38696583 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210520 MGI 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0012556 increased cell death IEA N RGD:5509061 20181011 MGI 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0012764 increased alpha-beta T cell number IEA N RGD:5509061 20190418 MGI 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20221103 MGI 736811 Pi4ka phosphatidylinositol 4-kinase alpha gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 736812 Cabin1 calcineurin binding protein 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 736812 Cabin1 calcineurin binding protein 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 736812 Cabin1 calcineurin binding protein 1 gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 736812 Cabin1 calcineurin binding protein 1 gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 736812 Cabin1 calcineurin binding protein 1 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:11714752 736812 Cabin1 calcineurin binding protein 1 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11714752 736812 Cabin1 calcineurin binding protein 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11714752 736812 Cabin1 calcineurin binding protein 1 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:11714752 736812 Cabin1 calcineurin binding protein 1 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:11714752 736812 Cabin1 calcineurin binding protein 1 gene MP:0011045 decreased lung elastance IEA N RGD:5509061 20230601 MGI 736812 Cabin1 calcineurin binding protein 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11714752 736812 Cabin1 calcineurin binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0001304 cataract IEA N RGD:5509061 20170105 MGI 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20200402 MGI 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0002546 mydriasis IEA N RGD:5509061 20160421 MGI 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0002833 increased heart weight IEA N RGD:5509061 20210128 MGI 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:7889569 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0003917 increased kidney weight IEA N RGD:5509061 20210128 MGI 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18687716 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22896717 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20160414 MGI PMID:26241901 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:18687716 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20160414 MGI PMID:26241901 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:18687716 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22895717 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:7889569 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0006243 impaired pupillary reflex IEA N RGD:5509061 20160421 MGI 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20160414 MGI PMID:26241901 736813 Grm6 glutamate receptor, metabotropic 6 gene MP:0012144 decreased b-wave amplitude IAGP N RGD:5509061 20170601 MGI PMID:28490646 736815 Hagh hydroxyacyl glutathione hydrolase gene MP:0000157 abnormal sternum morphology IEA N RGD:5509061 20230119 MGI 736815 Hagh hydroxyacyl glutathione hydrolase gene MP:0000208 decreased hematocrit IEA N RGD:5509061 20231207 MGI 736815 Hagh hydroxyacyl glutathione hydrolase gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20230119 MGI 736815 Hagh hydroxyacyl glutathione hydrolase gene MP:0001304 cataract IEA N RGD:5509061 20230119 MGI 736815 Hagh hydroxyacyl glutathione hydrolase gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20230119 MGI 736815 Hagh hydroxyacyl glutathione hydrolase gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20230119 MGI 736816 Mcpt1 mast cell protease 1 gene MP:0000359 abnormal mast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9708809 736816 Mcpt1 mast cell protease 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:15236182 736816 Mcpt1 mast cell protease 1 gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9708809 736816 Mcpt1 mast cell protease 1 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15236182 736816 Mcpt1 mast cell protease 1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15236182 736818 Ampd2 adenosine monophosphate deaminase 2 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20160324 MGI PMID:18974039 736818 Ampd2 adenosine monophosphate deaminase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23911318 736818 Ampd2 adenosine monophosphate deaminase 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20160324 MGI PMID:18974039 736818 Ampd2 adenosine monophosphate deaminase 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23911318 736818 Ampd2 adenosine monophosphate deaminase 2 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20160324 MGI PMID:18974039 736818 Ampd2 adenosine monophosphate deaminase 2 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:23911318 736818 Ampd2 adenosine monophosphate deaminase 2 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:22212473 736818 Ampd2 adenosine monophosphate deaminase 2 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:22212473 736818 Ampd2 adenosine monophosphate deaminase 2 gene MP:0003806 abnormal nucleotide metabolism IAGP N RGD:5509061 20141003 MGI PMID:23911318 736818 Ampd2 adenosine monophosphate deaminase 2 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20160324 MGI PMID:18974039 736818 Ampd2 adenosine monophosphate deaminase 2 gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20210128 MGI 736818 Ampd2 adenosine monophosphate deaminase 2 gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:22212473 736818 Ampd2 adenosine monophosphate deaminase 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23911318 736818 Ampd2 adenosine monophosphate deaminase 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 736823 Arg2 arginase type II gene MP:0000160 kyphosis IEA N RGD:5509061 20230119 MGI 736823 Arg2 arginase type II gene MP:0000162 lordosis IEA N RGD:5509061 20230119 MGI 736823 Arg2 arginase type II gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 736823 Arg2 arginase type II gene MP:0000274 enlarged heart IEA N RGD:5509061 20230119 MGI 736823 Arg2 arginase type II gene MP:0000277 abnormal heart shape IEA N RGD:5509061 20230119 MGI 736823 Arg2 arginase type II gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230119 MGI 736823 Arg2 arginase type II gene MP:0000692 small spleen IEA N RGD:5509061 20230119 MGI 736823 Arg2 arginase type II gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230119 MGI 736823 Arg2 arginase type II gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230119 MGI 736823 Arg2 arginase type II gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230119 MGI 736823 Arg2 arginase type II gene MP:0004174 abnormal spine curvature IEA N RGD:5509061 20230119 MGI 736823 Arg2 arginase type II gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20230119 MGI 736823 Arg2 arginase type II gene MP:0030661 increased circulating arginine level IAGP N RGD:5509061 20180913 MGI PMID:11154268 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:10531436 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:10798394 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:9636130 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10798394 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20210805 MGI PMID:34186026 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:10798394 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11257220 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:15071119 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:8893025 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0001984 abnormal olfaction IAGP N RGD:5509061 20141003 MGI PMID:15071119 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230601 MGI 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:10531436 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0002922 decreased post-tetanic potentiation IAGP N RGD:5509061 20141003 MGI PMID:9636130 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0003462 abnormal response to novel odor IAGP N RGD:5509061 20210805 MGI PMID:34186026 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0004512 anosmia IAGP N RGD:5509061 20141003 MGI PMID:8893025 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:10798394 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:10531436 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10798394 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11257220 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0010055 abnormal sensory neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:11257220 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8893025 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10798394 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10531436 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9636130 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20141218 MGI PMID:25411495 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20161222 MGI PMID:27916458 736825 Cnga2 cyclic nucleotide gated channel alpha 2 gene MP:0012014 abnormal olfactory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15186781 736828 Or51e2 olfactory receptor family 51 subfamily E member 2 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:17350283 736828 Or51e2 olfactory receptor family 51 subfamily E member 2 gene MP:0002739 abnormal olfactory bulb development IAGP N RGD:5509061 20141003 MGI PMID:19186165 736828 Or51e2 olfactory receptor family 51 subfamily E member 2 gene MP:0003438 abnormal carotid body physiology IAGP N RGD:5509061 20170720 MGI PMID:26560302 736828 Or51e2 olfactory receptor family 51 subfamily E member 2 gene MP:0005572 abnormal pulmonary respiratory rate IAGP N RGD:5509061 20170720 MGI PMID:26560302 736828 Or51e2 olfactory receptor family 51 subfamily E member 2 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:17350283 736828 Or51e2 olfactory receptor family 51 subfamily E member 2 gene MP:0020843 abnormal type I cell of carotid body physiology IAGP N RGD:5509061 20240801 MGI PMID:38706960 736830 Shh sonic hedgehog gene MP:0000033 absent scala media IAGP N RGD:5509061 20141003 MGI PMID:12231626 736830 Shh sonic hedgehog gene MP:0000041 absent endolymphatic duct IAGP N RGD:5509061 20141003 MGI PMID:12231626 736830 Shh sonic hedgehog gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:18213582 736830 Shh sonic hedgehog gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:17504941 736830 Shh sonic hedgehog gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:18213582 736830 Shh sonic hedgehog gene MP:0000090 absent premaxilla IAGP N RGD:5509061 20141003 MGI PMID:15576405 736830 Shh sonic hedgehog gene MP:0000094 absent alveolar process IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15576405 736830 Shh sonic hedgehog gene MP:0000118 arrest of tooth development IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0000128 growth retardation of molars IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 736830 Shh sonic hedgehog gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0000138 absent vertebrae IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0000141 abnormal vertebral body morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 736830 Shh sonic hedgehog gene MP:0000149 abnormal scapula morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0000163 abnormal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15841179 736830 Shh sonic hedgehog gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:15841179 736830 Shh sonic hedgehog gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20170314 MGI PMID:18617531 736830 Shh sonic hedgehog gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17504940 736830 Shh sonic hedgehog gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:17504940 736830 Shh sonic hedgehog gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24191021 736830 Shh sonic hedgehog gene MP:0000377 abnormal hair follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9768360 736830 Shh sonic hedgehog gene MP:0000378 absent hair follicles IAGP N RGD:5509061 20141003 MGI PMID:9768360 736830 Shh sonic hedgehog gene MP:0000383 abnormal hair follicle orientation IAGP N RGD:5509061 20141003 MGI PMID:9768360 736830 Shh sonic hedgehog gene MP:0000388 absent hair follicle inner root sheath IAGP N RGD:5509061 20141003 MGI PMID:9768360 736830 Shh sonic hedgehog gene MP:0000413 polyphalangy IAGP N RGD:5509061 20141106 MGI PMID:25034710 736830 Shh sonic hedgehog gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:9768360 736830 Shh sonic hedgehog gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:12756179 736830 Shh sonic hedgehog gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 736830 Shh sonic hedgehog gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:18213582 736830 Shh sonic hedgehog gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:20400693 736830 Shh sonic hedgehog gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23055936 736830 Shh sonic hedgehog gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:12756179 736830 Shh sonic hedgehog gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:16221724 736830 Shh sonic hedgehog gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:18694563 736830 Shh sonic hedgehog gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0000434 megacephaly IAGP N RGD:5509061 20141003 MGI PMID:11748151 736830 Shh sonic hedgehog gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0000445 short snout IAGP N RGD:5509061 20160324 MGI PMID:25373905 736830 Shh sonic hedgehog gene MP:0000453 absent mouth IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20221110 MGI PMID:33869166 736830 Shh sonic hedgehog gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16020517 736830 Shh sonic hedgehog gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20160324 MGI PMID:25373905 736830 Shh sonic hedgehog gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:10821773 736830 Shh sonic hedgehog gene MP:0000462 abnormal digestive system morphology IAGP N RGD:5509061 20141003 MGI PMID:20400693 736830 Shh sonic hedgehog gene MP:0000467 abnormal esophagus morphology IAGP N RGD:5509061 20141003 MGI PMID:10821773 736830 Shh sonic hedgehog gene MP:0000468 abnormal esophageal epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:21068065 736830 Shh sonic hedgehog gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10821773 736830 Shh sonic hedgehog gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:23873040 736830 Shh sonic hedgehog gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:10821773 736830 Shh sonic hedgehog gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:10821773 736830 Shh sonic hedgehog gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:12399320 736830 Shh sonic hedgehog gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:12399320 736830 Shh sonic hedgehog gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0000547 short limbs IAGP N RGD:5509061 20161216 MGI PMID:23644062 736830 Shh sonic hedgehog gene MP:0000551 absent forelimb IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0000554 abnormal carpal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16611729 736830 Shh sonic hedgehog gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0000557 absent hindlimb IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0000561 adactyly IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:16611729 736830 Shh sonic hedgehog gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:17400206 736830 Shh sonic hedgehog gene MP:0000562 polydactyly IAGP N RGD:5509061 20160324 MGI PMID:25373905 736830 Shh sonic hedgehog gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:15841179 736830 Shh sonic hedgehog gene MP:0000564 syndactyly IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:15075292 736830 Shh sonic hedgehog gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:15315763 736830 Shh sonic hedgehog gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:16120640 736830 Shh sonic hedgehog gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:17504940 736830 Shh sonic hedgehog gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:19223390 736830 Shh sonic hedgehog gene MP:0000565 oligodactyly IAGP N RGD:5509061 20141003 MGI PMID:22698544 736830 Shh sonic hedgehog gene MP:0000565 oligodactyly IAGP N RGD:5509061 20150205 MGI PMID:24715461 736830 Shh sonic hedgehog gene MP:0000566 synostosis IAGP N RGD:5509061 20141003 MGI PMID:17400206 736830 Shh sonic hedgehog gene MP:0000566 synostosis IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:17400206 736830 Shh sonic hedgehog gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20161216 MGI PMID:23644062 736830 Shh sonic hedgehog gene MP:0000596 abnormal liver development IAGP N RGD:5509061 20180215 MGI PMID:28432216 736830 Shh sonic hedgehog gene MP:0000639 abnormal adrenal gland morphology IAGP N RGD:5509061 20141003 MGI PMID:20118198 736830 Shh sonic hedgehog gene MP:0000646 enlarged adrenocortical cells IAGP N RGD:5509061 20141003 MGI PMID:20118198 736830 Shh sonic hedgehog gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:22841315 736830 Shh sonic hedgehog gene MP:0000767 abnormal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:10821773 736830 Shh sonic hedgehog gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:16221724 736830 Shh sonic hedgehog gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:19357274 736830 Shh sonic hedgehog gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16020517 736830 Shh sonic hedgehog gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0000783 abnormal forebrain morphology IAGP N RGD:5509061 20170314 MGI PMID:18617531 736830 Shh sonic hedgehog gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:18694563 736830 Shh sonic hedgehog gene MP:0000787 abnormal telencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0000808 abnormal hippocampus development IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0000820 abnormal choroid plexus morphology IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0000830 abnormal diencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:11748151 736830 Shh sonic hedgehog gene MP:0000837 abnormal hypothalamus morphology IAGP N RGD:5509061 20221110 MGI PMID:33869166 736830 Shh sonic hedgehog gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:15496441 736830 Shh sonic hedgehog gene MP:0000851 cerebellum hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19287388 736830 Shh sonic hedgehog gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0000854 abnormal cerebellum development IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0000872 abnormal cerebellum external granule cell layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19287388 736830 Shh sonic hedgehog gene MP:0000873 thin external granule cell layer IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0000886 abnormal cerebellar granule layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15496441 736830 Shh sonic hedgehog gene MP:0000889 abnormal cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:16020517 736830 Shh sonic hedgehog gene MP:0000897 abnormal midbrain morphology IAGP N RGD:5509061 20141003 MGI PMID:23444360 736830 Shh sonic hedgehog gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19223390 736830 Shh sonic hedgehog gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:21209331 736830 Shh sonic hedgehog gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:22698544 736830 Shh sonic hedgehog gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 736830 Shh sonic hedgehog gene MP:0000925 abnormal floor plate morphology IAGP N RGD:5509061 20141003 MGI PMID:22698544 736830 Shh sonic hedgehog gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:11748151 736830 Shh sonic hedgehog gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:15576405 736830 Shh sonic hedgehog gene MP:0000926 absent floor plate IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:21209331 736830 Shh sonic hedgehog gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:15105374 736830 Shh sonic hedgehog gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:11748151 736830 Shh sonic hedgehog gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15105374 736830 Shh sonic hedgehog gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:11748151 736830 Shh sonic hedgehog gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:15075292 736830 Shh sonic hedgehog gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20190912 MGI PMID:31305241 736830 Shh sonic hedgehog gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:11748151 736830 Shh sonic hedgehog gene MP:0000956 decreased spinal cord size IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0001046 abnormal enteric neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:10821773 736830 Shh sonic hedgehog gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:15305287 736830 Shh sonic hedgehog gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:24191021 736830 Shh sonic hedgehog gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:16452165 736830 Shh sonic hedgehog gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19686689 736830 Shh sonic hedgehog gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:23873040 736830 Shh sonic hedgehog gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:9768363 736830 Shh sonic hedgehog gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15305287 736830 Shh sonic hedgehog gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9768363 736830 Shh sonic hedgehog gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:19686689 736830 Shh sonic hedgehog gene MP:0001181 absent lungs IAGP N RGD:5509061 20141003 MGI PMID:23873040 736830 Shh sonic hedgehog gene MP:0001218 thin epidermis IAGP N RGD:5509061 20141003 MGI PMID:18262513 736830 Shh sonic hedgehog gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:9768360 736830 Shh sonic hedgehog gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9768360 736830 Shh sonic hedgehog gene MP:0001243 abnormal dermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9768360 736830 Shh sonic hedgehog gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19287388 736830 Shh sonic hedgehog gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19357274 736830 Shh sonic hedgehog gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:19502490 736830 Shh sonic hedgehog gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:12756179 736830 Shh sonic hedgehog gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:16020517 736830 Shh sonic hedgehog gene MP:0001293 anophthalmia IAGP N RGD:5509061 20141003 MGI PMID:18213582 736830 Shh sonic hedgehog gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:12195432 736830 Shh sonic hedgehog gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:12756179 736830 Shh sonic hedgehog gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:15105374 736830 Shh sonic hedgehog gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:16020517 736830 Shh sonic hedgehog gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:18213582 736830 Shh sonic hedgehog gene MP:0001297 microphthalmia IAGP N RGD:5509061 20141003 MGI PMID:19287388 736830 Shh sonic hedgehog gene MP:0001300 ocular hypertelorism IAGP N RGD:5509061 20230309 MGI PMID:23872235 736830 Shh sonic hedgehog gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:12195432 736830 Shh sonic hedgehog gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:12756179 736830 Shh sonic hedgehog gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:12756179 736830 Shh sonic hedgehog gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22841315 736830 Shh sonic hedgehog gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22841315 736830 Shh sonic hedgehog gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:22841315 736830 Shh sonic hedgehog gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 736830 Shh sonic hedgehog gene MP:0001622 abnormal vasculogenesis IAGP N RGD:5509061 20141003 MGI PMID:23873040 736830 Shh sonic hedgehog gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20400693 736830 Shh sonic hedgehog gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:15105374 736830 Shh sonic hedgehog gene MP:0001697 abnormal embryo size IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:11748151 736830 Shh sonic hedgehog gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15075292 736830 Shh sonic hedgehog gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17504940 736830 Shh sonic hedgehog gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170314 MGI PMID:18617531 736830 Shh sonic hedgehog gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17504940 736830 Shh sonic hedgehog gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15105374 736830 Shh sonic hedgehog gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15841179 736830 Shh sonic hedgehog gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:17881493 736830 Shh sonic hedgehog gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:17881493 736830 Shh sonic hedgehog gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:10821773 736830 Shh sonic hedgehog gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:17504940 736830 Shh sonic hedgehog gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16221724 736830 Shh sonic hedgehog gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:20118198 736830 Shh sonic hedgehog gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19223390 736830 Shh sonic hedgehog gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:19502490 736830 Shh sonic hedgehog gene MP:0001906 increased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22841315 736830 Shh sonic hedgehog gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20151112 MGI PMID:23358455 736830 Shh sonic hedgehog gene MP:0001953 respiratory failure IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22675208 736830 Shh sonic hedgehog gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:24191021 736830 Shh sonic hedgehog gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15576405 736830 Shh sonic hedgehog gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:18262513 736830 Shh sonic hedgehog gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:16221724 736830 Shh sonic hedgehog gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16020517 736830 Shh sonic hedgehog gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0002081 perinatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20400693 736830 Shh sonic hedgehog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19502490 736830 Shh sonic hedgehog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22841315 736830 Shh sonic hedgehog gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:20400693 736830 Shh sonic hedgehog gene MP:0002102 abnormal ear morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:15105374 736830 Shh sonic hedgehog gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:15841179 736830 Shh sonic hedgehog gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:17400206 736830 Shh sonic hedgehog gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20150205 MGI PMID:24715461 736830 Shh sonic hedgehog gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:16611729 736830 Shh sonic hedgehog gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:17400206 736830 Shh sonic hedgehog gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:19386268 736830 Shh sonic hedgehog gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15315763 736830 Shh sonic hedgehog gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:20400693 736830 Shh sonic hedgehog gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:20400693 736830 Shh sonic hedgehog gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15105374 736830 Shh sonic hedgehog gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:15576405 736830 Shh sonic hedgehog gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:19223390 736830 Shh sonic hedgehog gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:21209331 736830 Shh sonic hedgehog gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18272593 736830 Shh sonic hedgehog gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21192082 736830 Shh sonic hedgehog gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22841315 736830 Shh sonic hedgehog gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23328398 736830 Shh sonic hedgehog gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20170314 MGI PMID:18617531 736830 Shh sonic hedgehog gene MP:0002175 decreased brain weight IAGP N RGD:5509061 20141003 MGI PMID:19287388 736830 Shh sonic hedgehog gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20160324 MGI PMID:25373905 736830 Shh sonic hedgehog gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:17504941 736830 Shh sonic hedgehog gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:17344228 736830 Shh sonic hedgehog gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:18694563 736830 Shh sonic hedgehog gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 736830 Shh sonic hedgehog gene MP:0002234 abnormal pharynx morphology IAGP N RGD:5509061 20141003 MGI PMID:15305287 736830 Shh sonic hedgehog gene MP:0002237 abnormal nasal cavity morphology IAGP N RGD:5509061 20221110 MGI PMID:33869166 736830 Shh sonic hedgehog gene MP:0002257 abnormal arytenoid cartilage morphology IAGP N RGD:5509061 20180405 MGI PMID:19369396 736830 Shh sonic hedgehog gene MP:0002264 abnormal bronchus morphology IAGP N RGD:5509061 20141003 MGI PMID:15305287 736830 Shh sonic hedgehog gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20141003 MGI PMID:15305287 736830 Shh sonic hedgehog gene MP:0002282 abnormal trachea morphology IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0002284 abnormal tracheal smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9768363 736830 Shh sonic hedgehog gene MP:0002285 abnormal tracheal ciliated epithelium morphology IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0002543 brachyphalangia IAGP N RGD:5509061 20141003 MGI PMID:15841179 736830 Shh sonic hedgehog gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:15841179 736830 Shh sonic hedgehog gene MP:0002544 brachydactyly IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0002576 abnormal enamel morphology IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:17344228 736830 Shh sonic hedgehog gene MP:0002650 abnormal ameloblast morphology IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:20118198 736830 Shh sonic hedgehog gene MP:0002689 abnormal molar morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0002691 small stomach IAGP N RGD:5509061 20141003 MGI PMID:15829524 736830 Shh sonic hedgehog gene MP:0002726 abnormal pulmonary vein morphology IAGP N RGD:5509061 20141003 MGI PMID:23873040 736830 Shh sonic hedgehog gene MP:0002728 absent tibia IAGP N RGD:5509061 20141003 MGI PMID:17400206 736830 Shh sonic hedgehog gene MP:0002728 absent tibia IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:19287388 736830 Shh sonic hedgehog gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:17400206 736830 Shh sonic hedgehog gene MP:0002768 small adrenal glands IAGP N RGD:5509061 20141003 MGI PMID:20118198 736830 Shh sonic hedgehog gene MP:0002818 abnormal dentin morphology IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0002858 abnormal posterior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:12231626 736830 Shh sonic hedgehog gene MP:0002898 absent cartilage IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:23090636 736830 Shh sonic hedgehog gene MP:0002909 abnormal adrenal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:20118198 736830 Shh sonic hedgehog gene MP:0002932 abnormal joint morphology IAGP N RGD:5509061 20141003 MGI PMID:15841179 736830 Shh sonic hedgehog gene MP:0002948 abnormal neuron specification IAGP N RGD:5509061 20141003 MGI PMID:15269168 736830 Shh sonic hedgehog gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20141003 MGI PMID:17344228 736830 Shh sonic hedgehog gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:12399320 736830 Shh sonic hedgehog gene MP:0002990 short ureter IAGP N RGD:5509061 20141003 MGI PMID:12399320 736830 Shh sonic hedgehog gene MP:0003054 spina bifida IAGP N RGD:5509061 20141003 MGI PMID:19223390 736830 Shh sonic hedgehog gene MP:0003069 abnormal superior semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:12231626 736830 Shh sonic hedgehog gene MP:0003078 aphakia IAGP N RGD:5509061 20141003 MGI PMID:16020517 736830 Shh sonic hedgehog gene MP:0003115 abnormal respiratory system development IAGP N RGD:5509061 20141003 MGI PMID:22675208 736830 Shh sonic hedgehog gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15305287 736830 Shh sonic hedgehog gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9768363 736830 Shh sonic hedgehog gene MP:0003120 abnormal tracheal cartilage morphology IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0003130 anal atresia IAGP N RGD:5509061 20141003 MGI PMID:10821773 736830 Shh sonic hedgehog gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0003161 absent lateral semicircular canal IAGP N RGD:5509061 20141003 MGI PMID:12231626 736830 Shh sonic hedgehog gene MP:0003178 left pulmonary isomerism IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0003189 fused joints IAGP N RGD:5509061 20141003 MGI PMID:15841179 736830 Shh sonic hedgehog gene MP:0003244 loss of dopaminergic neurons IAGP N RGD:5509061 20141003 MGI PMID:22841315 736830 Shh sonic hedgehog gene MP:0003271 abnormal duodenum morphology IAGP N RGD:5509061 20141003 MGI PMID:10821773 736830 Shh sonic hedgehog gene MP:0003283 abnormal digestive organ placement IAGP N RGD:5509061 20141003 MGI PMID:10821773 736830 Shh sonic hedgehog gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:15305287 736830 Shh sonic hedgehog gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:19686689 736830 Shh sonic hedgehog gene MP:0003321 tracheoesophageal fistula IAGP N RGD:5509061 20141003 MGI PMID:9768363 736830 Shh sonic hedgehog gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0003424 premature neuronal precursor differentiation IAGP N RGD:5509061 20141003 MGI PMID:23444360 736830 Shh sonic hedgehog gene MP:0003425 abnormal optic vesicle formation IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12399320 736830 Shh sonic hedgehog gene MP:0003451 absent olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0003626 kidney medulla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12399320 736830 Shh sonic hedgehog gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:20400693 736830 Shh sonic hedgehog gene MP:0003634 abnormal glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12756179 736830 Shh sonic hedgehog gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:24191021 736830 Shh sonic hedgehog gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:12399320 736830 Shh sonic hedgehog gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20141003 MGI PMID:9768360 736830 Shh sonic hedgehog gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:23090636 736830 Shh sonic hedgehog gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20141003 MGI PMID:15576405 736830 Shh sonic hedgehog gene MP:0003793 abnormal submandibular gland morphology IAGP N RGD:5509061 20141003 MGI PMID:15042696 736830 Shh sonic hedgehog gene MP:0003809 abnormal hair shaft morphology IAGP N RGD:5509061 20141003 MGI PMID:9768360 736830 Shh sonic hedgehog gene MP:0003855 abnormal forelimb zeugopod morphology IAGP N RGD:5509061 20161216 MGI PMID:23644062 736830 Shh sonic hedgehog gene MP:0003857 abnormal hindlimb zeugopod morphology IAGP N RGD:5509061 20161216 MGI PMID:23644062 736830 Shh sonic hedgehog gene MP:0003885 abnormal rostral-caudal body axis extension IAGP N RGD:5509061 20141003 MGI PMID:17504940 736830 Shh sonic hedgehog gene MP:0003923 abnormal heart left atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:23873040 736830 Shh sonic hedgehog gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20230309 MGI PMID:23872235 736830 Shh sonic hedgehog gene MP:0003936 abnormal reproductive system development IAGP N RGD:5509061 20151112 MGI PMID:23358455 736830 Shh sonic hedgehog gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20160421 MGI 736830 Shh sonic hedgehog gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15105374 736830 Shh sonic hedgehog gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:23873040 736830 Shh sonic hedgehog gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9768363 736830 Shh sonic hedgehog gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0004100 abnormal spinal cord interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11748151 736830 Shh sonic hedgehog gene MP:0004101 abnormal brain interneuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16221724 736830 Shh sonic hedgehog gene MP:0004137 abnormal gastric surface mucous cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23090636 736830 Shh sonic hedgehog gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:17504941 736830 Shh sonic hedgehog gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:17881493 736830 Shh sonic hedgehog gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20170314 MGI PMID:18617531 736830 Shh sonic hedgehog gene MP:0004196 abnormal prenatal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:20400693 736830 Shh sonic hedgehog gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:10821773 736830 Shh sonic hedgehog gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:17504941 736830 Shh sonic hedgehog gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:15269168 736830 Shh sonic hedgehog gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:18694563 736830 Shh sonic hedgehog gene MP:0004268 abnormal optic stalk morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0004269 abnormal optic cup morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0004274 abnormal embryonic/fetal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:19287388 736830 Shh sonic hedgehog gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:19287388 736830 Shh sonic hedgehog gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:16221724 736830 Shh sonic hedgehog gene MP:0004276 abnormal medial ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0004277 abnormal lateral ganglionic eminence morphology IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0004313 absent vestibulocochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:12231626 736830 Shh sonic hedgehog gene MP:0004315 absent vestibular saccule IAGP N RGD:5509061 20141003 MGI PMID:12231626 736830 Shh sonic hedgehog gene MP:0004318 absent incus IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0004319 absent malleus IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0004354 absent deltoid tuberosity IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0004369 absent utricle IAGP N RGD:5509061 20141003 MGI PMID:12231626 736830 Shh sonic hedgehog gene MP:0004391 abnormal respiratory conducting tube morphology IAGP N RGD:5509061 20141003 MGI PMID:23873040 736830 Shh sonic hedgehog gene MP:0004419 absent parietal bone IAGP N RGD:5509061 20141003 MGI PMID:15576405 736830 Shh sonic hedgehog gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0004442 occipital bone foramen IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0004453 abnormal pterygoid bone morphology IAGP N RGD:5509061 20221110 MGI PMID:33869166 736830 Shh sonic hedgehog gene MP:0004460 alisphenoid bone hypoplasia IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0004461 basisphenoid bone hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:33869166 736830 Shh sonic hedgehog gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0004505 decreased renal glomerulus number IAGP N RGD:5509061 20141003 MGI PMID:12399320 736830 Shh sonic hedgehog gene MP:0004506 abnormal pubis morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0004507 abnormal ischium morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0004508 abnormal pectoral girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0004551 decreased tracheal cartilage ring number IAGP N RGD:5509061 20141003 MGI PMID:15305287 736830 Shh sonic hedgehog gene MP:0004553 absent tracheal cartilage rings IAGP N RGD:5509061 20141003 MGI PMID:15305287 736830 Shh sonic hedgehog gene MP:0004576 abnormal embryonic autopod plate morphology IAGP N RGD:5509061 20141003 MGI PMID:16120640 736830 Shh sonic hedgehog gene MP:0004620 cervical vertebral fusion IEA N RGD:5509061 20111116 MGI 736830 Shh sonic hedgehog gene MP:0004634 short metacarpal bones IAGP N RGD:5509061 20141003 MGI PMID:15841179 736830 Shh sonic hedgehog gene MP:0004658 abnormal ventral tubercle of atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0004712 notochord degeneration IAGP N RGD:5509061 20141003 MGI PMID:17504941 736830 Shh sonic hedgehog gene MP:0004712 notochord degeneration IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20141003 MGI PMID:18694563 736830 Shh sonic hedgehog gene MP:0004880 lung cyst IAGP N RGD:5509061 20141003 MGI PMID:15305287 736830 Shh sonic hedgehog gene MP:0004880 lung cyst IAGP N RGD:5509061 20141003 MGI PMID:24191021 736830 Shh sonic hedgehog gene MP:0004880 lung cyst IAGP N RGD:5509061 20160324 MGI PMID:25978641 736830 Shh sonic hedgehog gene MP:0004880 lung cyst IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0004882 enlarged lung IAGP N RGD:5509061 20160324 MGI PMID:25978641 736830 Shh sonic hedgehog gene MP:0004980 increased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:17504941 736830 Shh sonic hedgehog gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:17504941 736830 Shh sonic hedgehog gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:24191021 736830 Shh sonic hedgehog gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:16611729 736830 Shh sonic hedgehog gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:12195432 736830 Shh sonic hedgehog gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:12756179 736830 Shh sonic hedgehog gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:15075292 736830 Shh sonic hedgehog gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:15105374 736830 Shh sonic hedgehog gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:15269168 736830 Shh sonic hedgehog gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:17504940 736830 Shh sonic hedgehog gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:17504941 736830 Shh sonic hedgehog gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:18694563 736830 Shh sonic hedgehog gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:11748151 736830 Shh sonic hedgehog gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:15105374 736830 Shh sonic hedgehog gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:15576405 736830 Shh sonic hedgehog gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0005213 gastric metaplasia IAGP N RGD:5509061 20141003 MGI PMID:10821773 736830 Shh sonic hedgehog gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20201022 MGI 736830 Shh sonic hedgehog gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0005298 abnormal clavicle morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:15841179 736830 Shh sonic hedgehog gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:17400206 736830 Shh sonic hedgehog gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12399320 736830 Shh sonic hedgehog gene MP:0005352 small cranium IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0005359 growth retardation of incisors IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0005430 absent fibula IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0005493 stomach epithelial hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:10821773 736830 Shh sonic hedgehog gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:20400693 736830 Shh sonic hedgehog gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:23873040 736830 Shh sonic hedgehog gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20400693 736830 Shh sonic hedgehog gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:22841315 736830 Shh sonic hedgehog gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:17222543 736830 Shh sonic hedgehog gene MP:0005675 small gallbladder IAGP N RGD:5509061 20200227 MGI PMID:28432216 736830 Shh sonic hedgehog gene MP:0006030 abnormal otic vesicle development IAGP N RGD:5509061 20141003 MGI PMID:12231626 736830 Shh sonic hedgehog gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19056373 736830 Shh sonic hedgehog gene MP:0006097 abnormal cerebellar lobule formation IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0006098 absent cerebellar lobules IAGP N RGD:5509061 20141003 MGI PMID:15183722 736830 Shh sonic hedgehog gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:17344228 736830 Shh sonic hedgehog gene MP:0006197 ocular hypotelorism IAGP N RGD:5509061 20141003 MGI PMID:18694563 736830 Shh sonic hedgehog gene MP:0006261 annular pancreas IAGP N RGD:5509061 20141003 MGI PMID:10821773 736830 Shh sonic hedgehog gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20141003 MGI PMID:20386744 736830 Shh sonic hedgehog gene MP:0006279 abnormal limb development IAGP N RGD:5509061 20151112 MGI PMID:23358455 736830 Shh sonic hedgehog gene MP:0006281 abnormal tail development IAGP N RGD:5509061 20151112 MGI PMID:23358455 736830 Shh sonic hedgehog gene MP:0006290 proboscis IAGP N RGD:5509061 20141003 MGI PMID:15269168 736830 Shh sonic hedgehog gene MP:0006306 abnormal nasal pit morphology IAGP N RGD:5509061 20141003 MGI PMID:15576405 736830 Shh sonic hedgehog gene MP:0006306 abnormal nasal pit morphology IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:16452165 736830 Shh sonic hedgehog gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:24191021 736830 Shh sonic hedgehog gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20160324 MGI PMID:25978641 736830 Shh sonic hedgehog gene MP:0006382 abnormal lung epithelium morphology IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0006402 small molars IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0008004 abnormal stomach pH IAGP N RGD:5509061 20141003 MGI PMID:23090636 736830 Shh sonic hedgehog gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12756179 736830 Shh sonic hedgehog gene MP:0008291 abnormal adrenocortical cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20118198 736830 Shh sonic hedgehog gene MP:0008302 thin adrenal cortex IAGP N RGD:5509061 20141003 MGI PMID:20118198 736830 Shh sonic hedgehog gene MP:0008381 absent gonial bone IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21205797 736830 Shh sonic hedgehog gene MP:0008540 abnormal cerebral hemisphere morphology IAGP N RGD:5509061 20141003 MGI PMID:18694563 736830 Shh sonic hedgehog gene MP:0008947 increased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22841315 736830 Shh sonic hedgehog gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:22841315 736830 Shh sonic hedgehog gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:23444360 736830 Shh sonic hedgehog gene MP:0009204 absent external male genitalia IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0009211 absent external female genitalia IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0009467 abnormal magnocellular neurosecretory cell morphology IAGP N RGD:5509061 20221110 MGI PMID:33869166 736830 Shh sonic hedgehog gene MP:0009493 abnormal cystic duct morphology IAGP N RGD:5509061 20180215 MGI PMID:28432216 736830 Shh sonic hedgehog gene MP:0009545 abnormal dermis papillary layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9768360 736830 Shh sonic hedgehog gene MP:0009579 acephaly IAGP N RGD:5509061 20180215 MGI PMID:28432216 736830 Shh sonic hedgehog gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:9768363 736830 Shh sonic hedgehog gene MP:0009652 abnormal palatal rugae morphology IAGP N RGD:5509061 20191219 MGI PMID:31226309 736830 Shh sonic hedgehog gene MP:0009684 abnormal spinal cord lateral motor column morphology IAGP N RGD:5509061 20190912 MGI PMID:31305241 736830 Shh sonic hedgehog gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:19502490 736830 Shh sonic hedgehog gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:16611729 736830 Shh sonic hedgehog gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141106 MGI PMID:25034710 736830 Shh sonic hedgehog gene MP:0009744 postaxial polydactyly IAGP N RGD:5509061 20141106 MGI PMID:25034710 736830 Shh sonic hedgehog gene MP:0009844 abnormal neural crest cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17344228 736830 Shh sonic hedgehog gene MP:0009883 palatal shelf hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15199404 736830 Shh sonic hedgehog gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:15199404 736830 Shh sonic hedgehog gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:18694563 736830 Shh sonic hedgehog gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:15199404 736830 Shh sonic hedgehog gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0009900 vomer bone hypoplasia IAGP N RGD:5509061 20221110 MGI PMID:33869166 736830 Shh sonic hedgehog gene MP:0009901 abnormal frontonasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:15576405 736830 Shh sonic hedgehog gene MP:0009903 abnormal medial nasal prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:18694563 736830 Shh sonic hedgehog gene MP:0009905 absent tongue IAGP N RGD:5509061 20141003 MGI PMID:16020517 736830 Shh sonic hedgehog gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:15576405 736830 Shh sonic hedgehog gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 736830 Shh sonic hedgehog gene MP:0010030 abnormal orbit morphology IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0010059 olfactory bulb hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18694563 736830 Shh sonic hedgehog gene MP:0010116 abnormal primitive urogenital sinus morphology IAGP N RGD:5509061 20191219 MGI PMID:31669249 736830 Shh sonic hedgehog gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20160421 MGI 736830 Shh sonic hedgehog gene MP:0010125 abnormal parvocellular neurosecretory cell morphology IAGP N RGD:5509061 20221110 MGI PMID:33869166 736830 Shh sonic hedgehog gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20141003 MGI PMID:22841315 736830 Shh sonic hedgehog gene MP:0010493 abnormal atrium myocardium morphology IAGP N RGD:5509061 20141003 MGI PMID:23873040 736830 Shh sonic hedgehog gene MP:0010646 absent pulmonary vein IAGP N RGD:5509061 20141003 MGI PMID:23873040 736830 Shh sonic hedgehog gene MP:0010701 fusion of atlas and odontoid process IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0010784 abnormal forestomach morphology IAGP N RGD:5509061 20141003 MGI PMID:21068065 736830 Shh sonic hedgehog gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:9768363 736830 Shh sonic hedgehog gene MP:0010862 decreased respiratory mucosa goblet cell number IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0010883 trachea stenosis IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0010897 abnormal bronchiole epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19502490 736830 Shh sonic hedgehog gene MP:0010907 absent lung buds IAGP N RGD:5509061 20141003 MGI PMID:19686689 736830 Shh sonic hedgehog gene MP:0010915 increased solitary pulmonary neuroendocrine cell number IAGP N RGD:5509061 20141003 MGI PMID:19502490 736830 Shh sonic hedgehog gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20141003 MGI PMID:16020517 736830 Shh sonic hedgehog gene MP:0010942 abnormal respiratory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:19502490 736830 Shh sonic hedgehog gene MP:0010949 decreased club cell number IAGP N RGD:5509061 20141003 MGI PMID:22675208 736830 Shh sonic hedgehog gene MP:0010949 decreased club cell number IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:15305287 736830 Shh sonic hedgehog gene MP:0010976 small lung lobe IAGP N RGD:5509061 20141003 MGI PMID:16452165 736830 Shh sonic hedgehog gene MP:0010994 aerophagia IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0011011 impaired lung lobe morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:9768363 736830 Shh sonic hedgehog gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:15305287 736830 Shh sonic hedgehog gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:24191021 736830 Shh sonic hedgehog gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20160324 MGI PMID:25978641 736830 Shh sonic hedgehog gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0011028 impaired branching involved in bronchus morphogenesis IAGP N RGD:5509061 20141003 MGI PMID:9768363 736830 Shh sonic hedgehog gene MP:0011050 abnormal respiratory motile cilium morphology IAGP N RGD:5509061 20170803 MGI PMID:28675157 736830 Shh sonic hedgehog gene MP:0011071 absent club cells IAGP N RGD:5509061 20141003 MGI PMID:19502490 736830 Shh sonic hedgehog gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16221724 736830 Shh sonic hedgehog gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24191021 736830 Shh sonic hedgehog gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19502490 736830 Shh sonic hedgehog gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21205797 736830 Shh sonic hedgehog gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12195432 736830 Shh sonic hedgehog gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15075292 736830 Shh sonic hedgehog gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15305287 736830 Shh sonic hedgehog gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16611729 736830 Shh sonic hedgehog gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22675208 736830 Shh sonic hedgehog gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15576405 736830 Shh sonic hedgehog gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16452165 736830 Shh sonic hedgehog gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16611729 736830 Shh sonic hedgehog gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9768360 736830 Shh sonic hedgehog gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221110 MGI PMID:33869166 736830 Shh sonic hedgehog gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24191021 736830 Shh sonic hedgehog gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17504940 736830 Shh sonic hedgehog gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21068065 736830 Shh sonic hedgehog gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9768360 736830 Shh sonic hedgehog gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18272593 736830 Shh sonic hedgehog gene MP:0011113 abnormal airway basal cell morphology IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0011142 abnormal lung-associated mesenchyme development IAGP N RGD:5509061 20160324 MGI PMID:25978641 736830 Shh sonic hedgehog gene MP:0011142 abnormal lung-associated mesenchyme development IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0011147 increased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20160324 MGI PMID:25978641 736830 Shh sonic hedgehog gene MP:0011333 abnormal kidney inner medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:12399320 736830 Shh sonic hedgehog gene MP:0011360 kidney cortex hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:12399320 736830 Shh sonic hedgehog gene MP:0011378 abnormal kidney outer medulla inner stripe morphology IAGP N RGD:5509061 20141003 MGI PMID:12399320 736830 Shh sonic hedgehog gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0011415 abnormal aldosterone level IAGP N RGD:5509061 20141120 MGI PMID:21820362 736830 Shh sonic hedgehog gene MP:0011426 abnormal ureter smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:12399320 736830 Shh sonic hedgehog gene MP:0011485 abnormal urethra urothelium morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 736830 Shh sonic hedgehog gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:15105374 736830 Shh sonic hedgehog gene MP:0011771 abnormal genital tubercle morphology IAGP N RGD:5509061 20151112 MGI PMID:23358455 736830 Shh sonic hedgehog gene MP:0011805 decreased cell migration IAGP N RGD:5509061 20141003 MGI PMID:24191021 736830 Shh sonic hedgehog gene MP:0012089 decreased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0012091 increased midbrain size IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0012139 increased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:16357211 736830 Shh sonic hedgehog gene MP:0012139 increased forebrain size IAGP N RGD:5509061 20141003 MGI PMID:17468181 736830 Shh sonic hedgehog gene MP:0012197 impaired myofibroblast differentiation IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0012257 absent philtrum IAGP N RGD:5509061 20141003 MGI PMID:18694563 736830 Shh sonic hedgehog gene MP:0012270 cardiac edema IAGP N RGD:5509061 20141003 MGI PMID:17504940 736830 Shh sonic hedgehog gene MP:0012517 absent diencephalon IAGP N RGD:5509061 20141003 MGI PMID:8837770 736830 Shh sonic hedgehog gene MP:0013337 abnormal adenohypophysis development IAGP N RGD:5509061 20221110 MGI PMID:33869166 736830 Shh sonic hedgehog gene MP:0013338 abnormal neurohypophysis development IAGP N RGD:5509061 20221110 MGI PMID:33869166 736830 Shh sonic hedgehog gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20221110 MGI PMID:33869166 736830 Shh sonic hedgehog gene MP:0013358 ectopic neurohypophysis IAGP N RGD:5509061 20221110 MGI PMID:33869166 736830 Shh sonic hedgehog gene MP:0013790 single external naris IAGP N RGD:5509061 20150611 MGI PMID:17504940 736830 Shh sonic hedgehog gene MP:0013790 single external naris IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0014101 decreased chondrocyte proliferation IAGP N RGD:5509061 20171221 MGI PMID:15841179 736830 Shh sonic hedgehog gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20171221 MGI PMID:15841179 736830 Shh sonic hedgehog gene MP:0014155 absent olfactory epithelium IAGP N RGD:5509061 20160407 MGI PMID:16020517 736830 Shh sonic hedgehog gene MP:0014200 abnormal respiratory epithelium physiology IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0014280 forelimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:17504941 736830 Shh sonic hedgehog gene MP:0014281 hindlimb oligodactyly IAGP N RGD:5509061 20230810 MGI PMID:24415953 736830 Shh sonic hedgehog gene MP:0020516 abnormal visceral yolk sac mesenchyme morphology IAGP N RGD:5509061 20180125 MGI PMID:17881493 736830 Shh sonic hedgehog gene MP:0020530 disorganized thalamus IAGP N RGD:5509061 20180208 MGI PMID:19357274 736830 Shh sonic hedgehog gene MP:0021104 abnormal ventral interneuron 2 morphology IAGP N RGD:5509061 20220310 MGI PMID:15075292 736830 Shh sonic hedgehog gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:11748151 736830 Shh sonic hedgehog gene MP:0021105 abnormal ventral interneuron 3 morphology IAGP N RGD:5509061 20220310 MGI PMID:15075292 736830 Shh sonic hedgehog gene MP:0030002 increased lung apoptosis IAGP N RGD:5509061 20170622 MGI PMID:26329601 736830 Shh sonic hedgehog gene MP:0030079 small incisors IAGP N RGD:5509061 20170928 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20171005 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0030136 abnormal lower incisor morphology IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0030170 absent mandibular symphysis IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0030190 small snout IAGP N RGD:5509061 20171019 MGI PMID:16020517 736830 Shh sonic hedgehog gene MP:0030245 round head IAGP N RGD:5509061 20221110 MGI PMID:33869166 736830 Shh sonic hedgehog gene MP:0030250 frontonasal prominence hypoplasia IAGP N RGD:5509061 20171019 MGI PMID:16020517 736830 Shh sonic hedgehog gene MP:0030277 thin interparietal bone IAGP N RGD:5509061 20171102 MGI PMID:8270769 736830 Shh sonic hedgehog gene MP:0030350 premature coronal suture closure IAGP N RGD:5509061 20221201 MGI PMID:17525797 736830 Shh sonic hedgehog gene MP:0030453 abnormal odontoblast morphology IAGP N RGD:5509061 20171221 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0030457 abnormal molar cusp morphology IAGP N RGD:5509061 20171221 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0030527 absent enamel cord IAGP N RGD:5509061 20180118 MGI PMID:11044393 736830 Shh sonic hedgehog gene MP:0030892 epiglottis hypoplasia IAGP N RGD:5509061 20191219 MGI PMID:19369396 736830 Shh sonic hedgehog gene MP:0031021 abnormal gallbladder smooth muscle morphology IAGP N RGD:5509061 20200227 MGI PMID:28432216 736834 Matr3 matrin 3 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0000852 small cerebellum IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0000876 Purkinje cell degeneration IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0001263 weight loss IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0001393 ataxia IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0001513 limb grasping IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0001575 cyanosis IAGP N RGD:5509061 20210204 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20210204 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0002083 premature death IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0003354 astrocytosis IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0003387 aorta coarctation IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0004113 abnormal aortic arch morphology IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0004157 interrupted aortic arch IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0009400 decreased skeletal muscle fiber size IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0010047 axonal spheroids IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20210121 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0010429 abnormal heart left ventricle outflow tract morphology IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0010484 bicuspid aortic valve IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0010485 aortic arch hypoplasia IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0010527 bicuspid pulmonary valve IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20210204 MGI PMID:33082323 736834 Matr3 matrin 3 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0011666 double outlet right ventricle, ventricular defect committed to aorta IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0011668 double outlet right ventricle, Taussig bing type IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0012515 abnormal heart apex morphology IAGP N RGD:5509061 20160414 MGI PMID:25574029 736834 Matr3 matrin 3 gene MP:0020448 increased microglial cell activation IAGP N RGD:5509061 20210121 MGI PMID:33082323 736844 Podxl podocalyxin-like gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20160804 MGI PMID:25303643 736844 Podxl podocalyxin-like gene MP:0001183 overexpanded pulmonary alveolus IAGP N RGD:5509061 20160804 MGI PMID:25303643 736844 Podxl podocalyxin-like gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 736844 Podxl podocalyxin-like gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20160804 MGI PMID:25303643 736844 Podxl podocalyxin-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19837166 736844 Podxl podocalyxin-like gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:25303643 736844 Podxl podocalyxin-like gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:11435469 736844 Podxl podocalyxin-like gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11435469 736844 Podxl podocalyxin-like gene MP:0003052 omphalocele IAGP N RGD:5509061 20161229 MGI PMID:11435469 736844 Podxl podocalyxin-like gene MP:0003070 increased vascular permeability IAGP N RGD:5509061 20160804 MGI PMID:25303643 736844 Podxl podocalyxin-like gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20160804 MGI PMID:25303643 736844 Podxl podocalyxin-like gene MP:0003624 anuria IAGP N RGD:5509061 20141003 MGI PMID:11435469 736844 Podxl podocalyxin-like gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:19837166 736844 Podxl podocalyxin-like gene MP:0004181 abnormal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:19837166 736844 Podxl podocalyxin-like gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20141003 MGI PMID:11435469 736844 Podxl podocalyxin-like gene MP:0008138 absent podocyte foot process IAGP N RGD:5509061 20141003 MGI PMID:11435469 736844 Podxl podocalyxin-like gene MP:0010935 increased airway resistance IAGP N RGD:5509061 20160804 MGI PMID:25303643 736844 Podxl podocalyxin-like gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11435469 736844 Podxl podocalyxin-like gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20210603 MGI PMID:27542690 736844 Podxl podocalyxin-like gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736844 Podxl podocalyxin-like gene MP:0011136 increased lung endothelial cell adhesion IAGP N RGD:5509061 20160804 MGI PMID:25303643 736844 Podxl podocalyxin-like gene MP:0011137 decreased lung endothelial cell adhesion IAGP N RGD:5509061 20160804 MGI PMID:25303643 736844 Podxl podocalyxin-like gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:19837166 736844 Podxl podocalyxin-like gene MP:0011641 abnormal pulmonary collagen fibril morphology IAGP N RGD:5509061 20160804 MGI PMID:25303643 736848 Capza3 capping actin protein of muscle Z-line subunit alpha 3 gene MP:0001925 male infertility IEA N RGD:5509061 20111116 MGI 736848 Capza3 capping actin protein of muscle Z-line subunit alpha 3 gene MP:0001932 abnormal spermiogenesis IEA N RGD:5509061 20111116 MGI 736848 Capza3 capping actin protein of muscle Z-line subunit alpha 3 gene MP:0002675 asthenozoospermia IEA N RGD:5509061 20220714 MGI 736848 Capza3 capping actin protein of muscle Z-line subunit alpha 3 gene MP:0002687 oligozoospermia IEA N RGD:5509061 20220714 MGI 736848 Capza3 capping actin protein of muscle Z-line subunit alpha 3 gene MP:0008892 abnormal sperm flagellum morphology IEA N RGD:5509061 20220714 MGI 736848 Capza3 capping actin protein of muscle Z-line subunit alpha 3 gene MP:0009230 abnormal sperm head morphology IEA N RGD:5509061 20220714 MGI 736849 Cox4i1 cytochrome c oxidase subunit 4I1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20210128 MGI 736849 Cox4i1 cytochrome c oxidase subunit 4I1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 736849 Cox4i1 cytochrome c oxidase subunit 4I1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 736849 Cox4i1 cytochrome c oxidase subunit 4I1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 736851 Atp2c1 ATPase, Ca++-sequestering gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17597066 736851 Atp2c1 ATPase, Ca++-sequestering gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:17597066 736851 Atp2c1 ATPase, Ca++-sequestering gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:17597066 736851 Atp2c1 ATPase, Ca++-sequestering gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:17597066 736851 Atp2c1 ATPase, Ca++-sequestering gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:17597066 736851 Atp2c1 ATPase, Ca++-sequestering gene MP:0003277 increased esophageal papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:17597066 736851 Atp2c1 ATPase, Ca++-sequestering gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17597066 736851 Atp2c1 ATPase, Ca++-sequestering gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17597066 736851 Atp2c1 ATPase, Ca++-sequestering gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:17597066 736851 Atp2c1 ATPase, Ca++-sequestering gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:17597066 736851 Atp2c1 ATPase, Ca++-sequestering gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17597066 736851 Atp2c1 ATPase, Ca++-sequestering gene MP:0011743 abnormal Golgi apparatus morphology IAGP N RGD:5509061 20141003 MGI PMID:17597066 736851 Atp2c1 ATPase, Ca++-sequestering gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17597066 736851 Atp2c1 ATPase, Ca++-sequestering gene MP:0013199 increased head mesenchyme apoptosis IAGP N RGD:5509061 20190704 MGI PMID:17597066 736856 Pkib protein kinase inhibitor beta, cAMP dependent, testis specific gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11359903 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0000032 cochlear degeneration IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:16181686 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21947296 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:21947296 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0001327 decreased retina photoreceptor cell number IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:21947296 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0002001 blindness IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:21947296 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0002857 cochlear ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:16181686 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0002864 abnormal ocular fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21947296 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004043 abnormal pH regulation IAGP N RGD:5509061 20141003 MGI PMID:18077606 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004288 abnormal spiral ligament morphology IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004292 abnormal spiral ligament fibrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16181686 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004293 abnormal type I spiral ligament fibrocytes IAGP N RGD:5509061 20141003 MGI PMID:16181686 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16181686 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004398 cochlear inner hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16181686 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:16181686 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004430 abnormal Claudius cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16181686 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:16181686 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004488 type II spiral ligament fibrocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:16181686 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004490 type IV spiral ligament fibrocyte degeneration IAGP N RGD:5509061 20141003 MGI PMID:16181686 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21947296 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:21947296 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21947296 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0006024 collapsed Reissner membrane IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0008584 photoreceptor outer segment degeneration IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21947296 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:12808454 736860 Slc4a7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12808454 736862 Rap2b RAP2B, member of RAS oncogene family gene MP:0001399 hyperactivity IEA N RGD:5509061 20170105 MGI 736862 Rap2b RAP2B, member of RAS oncogene family gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201231 MGI 736862 Rap2b RAP2B, member of RAS oncogene family gene MP:0001516 abnormal motor coordination/balance IEA N RGD:5509061 20201022 MGI 736862 Rap2b RAP2B, member of RAS oncogene family gene MP:0004151 decreased circulating iron level IEA N RGD:5509061 20220519 MGI 736862 Rap2b RAP2B, member of RAS oncogene family gene MP:0004924 abnormal behavior IEA N RGD:5509061 20170105 MGI 736862 Rap2b RAP2B, member of RAS oncogene family gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20220519 MGI 736862 Rap2b RAP2B, member of RAS oncogene family gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20201022 MGI 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0000781 decreased corpus callosum size IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0000960 abnormal sensory ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0001011 abnormal superior cervical ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0001083 small geniculate ganglion IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20160811 MGI 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0001513 limb grasping IEA N RGD:5509061 20201022 MGI 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0002199 abnormal brain commissure morphology IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0002574 increased vertical activity IEA N RGD:5509061 20220519 MGI 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0002631 abnormal epididymis morphology IEA N RGD:5509061 20160811 MGI 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210520 MGI 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0004267 abnormal optic tract morphology IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0004298 vestibular ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0004924 abnormal behavior IEA N RGD:5509061 20211021 MGI 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0004931 enlarged epididymis IEA N RGD:5509061 20160811 MGI 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0006409 vestibular ganglion hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0008223 absent hippocampal commissure IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0008227 absent anterior commissure IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0008492 dorsal root ganglion degeneration IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0008535 enlarged lateral ventricles IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20230601 MGI 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0011380 enlarged brain ventricles IAGP N RGD:5509061 20141003 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0020548 decreased optic chiasm size IAGP N RGD:5509061 20180301 MGI PMID:21262811 736864 Vti1a vesicle transport through interaction with t-SNAREs 1A gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20211021 MGI 736867 Abcc3 ATP-binding cassette, sub-family C member 3 gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:15886284 736867 Abcc3 ATP-binding cassette, sub-family C member 3 gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:15814571 736867 Abcc3 ATP-binding cassette, sub-family C member 3 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:15814571 736867 Abcc3 ATP-binding cassette, sub-family C member 3 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16225954 736867 Abcc3 ATP-binding cassette, sub-family C member 3 gene MP:0005365 abnormal bile salt homeostasis IAGP N RGD:5509061 20141003 MGI PMID:18292224 736867 Abcc3 ATP-binding cassette, sub-family C member 3 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:15886284 736869 Trim9 tripartite motif-containing 9 gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20150910 MGI PMID:24778312 736869 Trim9 tripartite motif-containing 9 gene MP:0001158 abnormal prostate gland morphology IEA N RGD:5509061 20200514 MGI 736869 Trim9 tripartite motif-containing 9 gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20200514 MGI 736869 Trim9 tripartite motif-containing 9 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 736869 Trim9 tripartite motif-containing 9 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 736869 Trim9 tripartite motif-containing 9 gene MP:0002774 small prostate gland IEA N RGD:5509061 20200514 MGI 736869 Trim9 tripartite motif-containing 9 gene MP:0003068 enlarged kidney IEA N RGD:5509061 20200514 MGI 736869 Trim9 tripartite motif-containing 9 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20200514 MGI 736869 Trim9 tripartite motif-containing 9 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20150910 MGI PMID:24778312 736869 Trim9 tripartite motif-containing 9 gene MP:0004953 decreased spleen weight IEA N RGD:5509061 20201022 MGI 736869 Trim9 tripartite motif-containing 9 gene MP:0005634 decreased circulating sodium level IEA N RGD:5509061 20200514 MGI 736869 Trim9 tripartite motif-containing 9 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20150910 MGI PMID:24778312 736869 Trim9 tripartite motif-containing 9 gene MP:0012443 increased corpus callosum size IAGP N RGD:5509061 20150910 MGI PMID:24778312 736869 Trim9 tripartite motif-containing 9 gene MP:0013771 decreased effector memory T-helper cell number IEA N RGD:5509061 20210520 MGI 736870 Arfrp1 ADP-ribosylation factor related protein 1 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:11839814 736870 Arfrp1 ADP-ribosylation factor related protein 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18662990 736870 Arfrp1 ADP-ribosylation factor related protein 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11839814 736870 Arfrp1 ADP-ribosylation factor related protein 1 gene MP:0011207 absent ectoplacental cavity IAGP N RGD:5509061 20141003 MGI PMID:11839814 736870 Arfrp1 ADP-ribosylation factor related protein 1 gene MP:0011209 absent extraembryonic coelom IAGP N RGD:5509061 20141003 MGI PMID:11839814 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20167925 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:17084362 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:17084362 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0001211 wrinkled skin IAGP N RGD:5509061 20141003 MGI PMID:20167925 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:17084362 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20167925 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:17084362 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:20167925 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:17084362 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17084362 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:17084362 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0003051 curly tail IAGP N RGD:5509061 20141003 MGI PMID:20167925 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0003122 maternal imprinting IAGP N RGD:5509061 20141003 MGI PMID:17084362 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0003123 paternal imprinting IAGP N RGD:5509061 20160428 MGI PMID:20167925 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:20167925 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0005109 abnormal talus morphology IAGP N RGD:5509061 20141003 MGI PMID:17084362 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:17084362 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17084362 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:20167925 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:17084362 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:17084362 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:20167925 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:20167925 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20167925 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17084362 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20167925 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17084362 736873 Plagl1 pleiomorphic adenoma gene-like 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20167925 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:18268345 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18268345 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:18268345 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:18268345 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:18268345 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:18268345 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0002919 enhanced paired-pulse facilitation IAGP N RGD:5509061 20210715 MGI PMID:32252022 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20210715 MGI PMID:32252022 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0004770 abnormal synaptic vesicle recycling IAGP N RGD:5509061 20210715 MGI PMID:32252022 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:18268345 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20111116 MGI 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:18268345 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20210715 MGI PMID:32252022 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20210715 MGI PMID:32252022 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0013600 testis degeneration IEA N RGD:5509061 20150312 MGI 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0030950 abnormal synaptic vesicle exocytosis IAGP N RGD:5509061 20210715 MGI PMID:32252022 736874 Ip6k1 inositol hexaphosphate kinase 1 gene MP:0030951 abnormal endocytosis IAGP N RGD:5509061 20210715 MGI PMID:32252022 736876 Rab4b RAB4B, member RAS oncogene family gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20220811 MGI 736876 Rab4b RAB4B, member RAS oncogene family gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20220811 MGI 736878 Clasp2 CLIP associating protein 2 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:17113391 736878 Clasp2 CLIP associating protein 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17113391 736879 Ptgfrn prostaglandin F2 receptor negative regulator gene MP:0003360 abnormal depression-related behavior IEA N RGD:5509061 20141003 MGI 736880 Scn7a sodium channel, voltage-gated, type VII, alpha gene MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11027237 736880 Scn7a sodium channel, voltage-gated, type VII, alpha gene MP:0001986 abnormal taste sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12650985 736883 Adcy5 adenylate cyclase 5 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12665504 736883 Adcy5 adenylate cyclase 5 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12665504 736883 Adcy5 adenylate cyclase 5 gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:12665504 736883 Adcy5 adenylate cyclase 5 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:12665504 736883 Adcy5 adenylate cyclase 5 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:12665504 736883 Adcy5 adenylate cyclase 5 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:12223546 736887 Hpgd hydroxyprostaglandin dehydrogenase 15 (NAD) gene MP:0000364 abnormal vascular regression IAGP N RGD:5509061 20141003 MGI PMID:11821873 736887 Hpgd hydroxyprostaglandin dehydrogenase 15 (NAD) gene MP:0002679 abnormal corpus luteum morphology IAGP N RGD:5509061 20141003 MGI PMID:17872381 736887 Hpgd hydroxyprostaglandin dehydrogenase 15 (NAD) gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:11821873 736887 Hpgd hydroxyprostaglandin dehydrogenase 15 (NAD) gene MP:0005186 increased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:17872381 736887 Hpgd hydroxyprostaglandin dehydrogenase 15 (NAD) gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:11821873 736887 Hpgd hydroxyprostaglandin dehydrogenase 15 (NAD) gene MP:0009811 abnormal prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:15542609 736887 Hpgd hydroxyprostaglandin dehydrogenase 15 (NAD) gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:11821873 736887 Hpgd hydroxyprostaglandin dehydrogenase 15 (NAD) gene MP:0009814 increased prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:17872381 736887 Hpgd hydroxyprostaglandin dehydrogenase 15 (NAD) gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11821873 736887 Hpgd hydroxyprostaglandin dehydrogenase 15 (NAD) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 736887 Hpgd hydroxyprostaglandin dehydrogenase 15 (NAD) gene MP:0012009 early parturition IAGP N RGD:5509061 20141003 MGI PMID:17872381 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:10734066 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:12149271 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:23903354 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:12035032 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:12149271 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:23903354 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:12035032 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20220811 MGI 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23903354 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:10734066 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12149271 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23903354 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12035032 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23903354 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12035032 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23903354 736889 Abcc8 ATP-binding cassette, sub-family C member 8 gene MP:0020345 abnormal myocardial fiber currents IAGP N RGD:5509061 20211202 MGI PMID:33529173 736891 Gmfg glia maturation factor, gamma gene MP:0002494 increased IgM level IAGP N RGD:5509061 20241024 MGI PMID:34673932 736891 Gmfg glia maturation factor, gamma gene MP:0008193 abnormal marginal zone B cell physiology IAGP N RGD:5509061 20241024 MGI PMID:34673932 736891 Gmfg glia maturation factor, gamma gene MP:0014472 impaired B cell migration IAGP N RGD:5509061 20241024 MGI PMID:34673932 736891 Gmfg glia maturation factor, gamma gene MP:0031207 decreased lymphocyte chemotaxis IAGP N RGD:5509061 20241024 MGI PMID:34673932 736893 Acox3 acyl-Coenzyme A oxidase 3, pristanoyl gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 736893 Acox3 acyl-Coenzyme A oxidase 3, pristanoyl gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 736893 Acox3 acyl-Coenzyme A oxidase 3, pristanoyl gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20220811 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0000496 abnormal small intestine morphology IEA N RGD:5509061 20170504 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0000940 abnormal motor neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:15173594 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:15173594 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15173594 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:15173594 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0002073 abnormal hair growth IEA N RGD:5509061 20201022 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20170504 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20170504 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0004836 abnormal synaptic acetylcholine release IAGP N RGD:5509061 20141003 MGI PMID:15173594 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:15173594 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0009144 dilated pancreatic duct IEA N RGD:5509061 20170504 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15173594 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20211021 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0010052 increased grip strength IEA N RGD:5509061 20150430 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20211021 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20170504 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0010484 bicuspid aortic valve IEA N RGD:5509061 20170504 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0010912 herniated liver IEA N RGD:5509061 20170504 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15173594 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0013975 abnormal coronary sinus connection IEA N RGD:5509061 20170504 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 736894 Slc5a7 solute carrier family 5 (choline transporter), member 7 gene MP:0014087 retrolental blood IEA N RGD:5509061 20180628 MGI 736895 Timm23 translocase of inner mitochondrial membrane 23 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:19111522 736895 Timm23 translocase of inner mitochondrial membrane 23 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:19111522 736895 Timm23 translocase of inner mitochondrial membrane 23 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:19111522 736895 Timm23 translocase of inner mitochondrial membrane 23 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19111522 736895 Timm23 translocase of inner mitochondrial membrane 23 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19111522 736895 Timm23 translocase of inner mitochondrial membrane 23 gene MP:0003786 premature aging IAGP N RGD:5509061 20141003 MGI PMID:19111522 736895 Timm23 translocase of inner mitochondrial membrane 23 gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:19111522 736895 Timm23 translocase of inner mitochondrial membrane 23 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19111522 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20180614 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20180614 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20210826 MGI 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20180614 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20180614 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20181220 MGI PMID:25581363 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20180614 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20180614 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20180614 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20211021 MGI 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0003201 extremity edema IAGP N RGD:5509061 20180614 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20180614 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20180614 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20180614 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20180614 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20181220 MGI PMID:25581363 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20181220 MGI PMID:25581363 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0010500 myocardium hypoplasia IAGP N RGD:5509061 20180614 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20231221 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20180614 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20180614 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20211021 MGI 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0014365 impaired short-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:25581363 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0014367 impaired long-term object recognition memory IAGP N RGD:5509061 20240328 MGI PMID:25581363 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0014518 myocardial hypertrabeculation IAGP N RGD:5509061 20240822 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0014519 myocardial ventricular hypertrabeculation IAGP N RGD:5509061 20240822 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20181220 MGI PMID:25581363 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231221 MGI PMID:29632206 736896 Nae1 NEDD8 activating enzyme E1 subunit 1 gene MP:0031525 thin left ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:29632206 736903 Fgf17 fibroblast growth factor 17 gene MP:0000864 abnormal cerebellum vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:10751172 736903 Fgf17 fibroblast growth factor 17 gene MP:0000867 abnormal cerebellum anterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:10751172 736903 Fgf17 fibroblast growth factor 17 gene MP:0000867 abnormal cerebellum anterior vermis morphology IAGP N RGD:5509061 20141003 MGI PMID:19968985 736903 Fgf17 fibroblast growth factor 17 gene MP:0000868 decreased anterior vermis size IAGP N RGD:5509061 20141003 MGI PMID:10751172 736903 Fgf17 fibroblast growth factor 17 gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10751172 736903 Fgf17 fibroblast growth factor 17 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:10751172 736903 Fgf17 fibroblast growth factor 17 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:10751172 736903 Fgf17 fibroblast growth factor 17 gene MP:0009038 decreased inferior colliculus size IAGP N RGD:5509061 20141003 MGI PMID:19968985 736903 Fgf17 fibroblast growth factor 17 gene MP:0010052 increased grip strength IEA N RGD:5509061 20230601 MGI 736904 Homer2 homer scaffolding protein 2 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:15294147 736904 Homer2 homer scaffolding protein 2 gene MP:0002556 abnormal cocaine consumption IAGP N RGD:5509061 20141003 MGI PMID:15294147 736904 Homer2 homer scaffolding protein 2 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:12860966 736904 Homer2 homer scaffolding protein 2 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:22561452 736904 Homer2 homer scaffolding protein 2 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15294147 736904 Homer2 homer scaffolding protein 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 736904 Homer2 homer scaffolding protein 2 gene MP:0009713 enhanced conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:15294147 736904 Homer2 homer scaffolding protein 2 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:15294147 736904 Homer2 homer scaffolding protein 2 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20230601 MGI 736907 Hrg histidine-rich glycoprotein gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15869579 736907 Hrg histidine-rich glycoprotein gene MP:0003422 abnormal thrombolysis IAGP N RGD:5509061 20141003 MGI PMID:15869579 736907 Hrg histidine-rich glycoprotein gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:15869579 736907 Hrg histidine-rich glycoprotein gene MP:0012331 increased circulating fibrinogen level IAGP N RGD:5509061 20200618 MGI PMID:15869579 736907 Hrg histidine-rich glycoprotein gene MP:0012355 decreased prothrombin time IAGP N RGD:5509061 20200618 MGI PMID:15869579 736908 Spr sepiapterin reductase gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 736908 Spr sepiapterin reductase gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:18201550 736908 Spr sepiapterin reductase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18201550 736908 Spr sepiapterin reductase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:18201550 736908 Spr sepiapterin reductase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16532389 736908 Spr sepiapterin reductase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18201550 736908 Spr sepiapterin reductase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16532389 736908 Spr sepiapterin reductase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18201550 736908 Spr sepiapterin reductase gene MP:0002204 abnormal synaptic neurotransmitter level IAGP N RGD:5509061 20141003 MGI PMID:16532389 736908 Spr sepiapterin reductase gene MP:0003243 abnormal dopaminergic neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:16532389 736908 Spr sepiapterin reductase gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16532389 736908 Spr sepiapterin reductase gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:16532389 736908 Spr sepiapterin reductase gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:18201550 736908 Spr sepiapterin reductase gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:16532389 736908 Spr sepiapterin reductase gene MP:0005320 abnormal biopterin level IAGP N RGD:5509061 20141003 MGI PMID:16532389 736908 Spr sepiapterin reductase gene MP:0005320 abnormal biopterin level IAGP N RGD:5509061 20141003 MGI PMID:18201550 736908 Spr sepiapterin reductase gene MP:0005321 abnormal neopterin level IAGP N RGD:5509061 20141003 MGI PMID:16532389 736908 Spr sepiapterin reductase gene MP:0005321 abnormal neopterin level IAGP N RGD:5509061 20141003 MGI PMID:18201550 736908 Spr sepiapterin reductase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:16532389 736908 Spr sepiapterin reductase gene MP:0005643 decreased dopamine level IAGP N RGD:5509061 20141003 MGI PMID:18201550 736908 Spr sepiapterin reductase gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 736908 Spr sepiapterin reductase gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:16532389 736908 Spr sepiapterin reductase gene MP:0010070 decreased serotonin level IAGP N RGD:5509061 20180920 MGI PMID:18201550 736908 Spr sepiapterin reductase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 736908 Spr sepiapterin reductase gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18201550 736908 Spr sepiapterin reductase gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20180920 MGI PMID:16532389 736908 Spr sepiapterin reductase gene MP:0012574 decreased noradrenaline level IAGP N RGD:5509061 20180920 MGI PMID:18201550 736908 Spr sepiapterin reductase gene MP:0030670 increased circulating phenylalanine level IAGP N RGD:5509061 20180920 MGI PMID:16532389 736908 Spr sepiapterin reductase gene MP:0030698 decreased phenylalanine level IAGP N RGD:5509061 20180927 MGI PMID:18201550 736910 Trim17 tripartite motif-containing 17 gene MP:0004509 abnormal pelvic girdle bone morphology IEA N RGD:5509061 20210128 MGI 736911 S100a1 S100 calcium binding protein A1 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20230601 MGI 736911 S100a1 S100 calcium binding protein A1 gene MP:0001147 small testis IEA N RGD:5509061 20230601 MGI 736911 S100a1 S100 calcium binding protein A1 gene MP:0001148 enlarged testis IEA N RGD:5509061 20230601 MGI 736911 S100a1 S100 calcium binding protein A1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20230601 MGI 736911 S100a1 S100 calcium binding protein A1 gene MP:0001304 cataract IEA N RGD:5509061 20230601 MGI 736911 S100a1 S100 calcium binding protein A1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:17045663 736911 S100a1 S100 calcium binding protein A1 gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:17045663 736911 S100a1 S100 calcium binding protein A1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20230601 MGI 736911 S100a1 S100 calcium binding protein A1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:18089560 736911 S100a1 S100 calcium binding protein A1 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 736911 S100a1 S100 calcium binding protein A1 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:17045663 736911 S100a1 S100 calcium binding protein A1 gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20230601 MGI 736911 S100a1 S100 calcium binding protein A1 gene MP:0003034 increased pulmonary vascular resistance IAGP N RGD:5509061 20160505 MGI PMID:25395393 736911 S100a1 S100 calcium binding protein A1 gene MP:0003461 abnormal response to novel object IAGP N RGD:5509061 20141003 MGI PMID:17045663 736911 S100a1 S100 calcium binding protein A1 gene MP:0003548 pulmonary hypertension IAGP N RGD:5509061 20160505 MGI PMID:25395393 736911 S100a1 S100 calcium binding protein A1 gene MP:0003820 increased left ventricle systolic pressure IAGP N RGD:5509061 20160505 MGI PMID:25395393 736911 S100a1 S100 calcium binding protein A1 gene MP:0003913 increased heart right ventricle weight IAGP N RGD:5509061 20160505 MGI PMID:25395393 736911 S100a1 S100 calcium binding protein A1 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20160505 MGI PMID:25395393 736911 S100a1 S100 calcium binding protein A1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20160505 MGI PMID:25395393 736911 S100a1 S100 calcium binding protein A1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 736911 S100a1 S100 calcium binding protein A1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11909974 736911 S100a1 S100 calcium binding protein A1 gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20160505 MGI PMID:25395393 736911 S100a1 S100 calcium binding protein A1 gene MP:0010758 increased right ventricle systolic pressure IAGP N RGD:5509061 20160505 MGI PMID:25395393 736911 S100a1 S100 calcium binding protein A1 gene MP:0011131 abnormal lung endothelial cell physiology IAGP N RGD:5509061 20160505 MGI PMID:25395393 736911 S100a1 S100 calcium binding protein A1 gene MP:0011141 increased lung endothelial cell apoptosis IAGP N RGD:5509061 20160505 MGI PMID:25395393 736913 Nbl1 NBL1, DAN family BMP antagonist gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:15033178 736913 Nbl1 NBL1, DAN family BMP antagonist gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11134349 736913 Nbl1 NBL1, DAN family BMP antagonist gene MP:0004616 lumbar vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:11134349 736924 Bckdhb branched chain ketoacid dehydrogenase E1, beta polypeptide gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20240222 MGI PMID:36880392 736924 Bckdhb branched chain ketoacid dehydrogenase E1, beta polypeptide gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20240222 MGI PMID:36880392 736924 Bckdhb branched chain ketoacid dehydrogenase E1, beta polypeptide gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20240222 MGI PMID:36880392 736924 Bckdhb branched chain ketoacid dehydrogenase E1, beta polypeptide gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 736924 Bckdhb branched chain ketoacid dehydrogenase E1, beta polypeptide gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20240222 MGI PMID:36880392 736924 Bckdhb branched chain ketoacid dehydrogenase E1, beta polypeptide gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736924 Bckdhb branched chain ketoacid dehydrogenase E1, beta polypeptide gene MP:0030674 decreased circulating alanine level IAGP N RGD:5509061 20240222 MGI PMID:36880392 736924 Bckdhb branched chain ketoacid dehydrogenase E1, beta polypeptide gene MP:0030727 increased circulating valine level IAGP N RGD:5509061 20240222 MGI PMID:36880392 736924 Bckdhb branched chain ketoacid dehydrogenase E1, beta polypeptide gene MP:0030750 increased circulating leucine level IAGP N RGD:5509061 20240222 MGI PMID:36880392 736928 Ppp2cb protein phosphatase 2 (formerly 2A), catalytic subunit, beta isoform gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21998041 736928 Ppp2cb protein phosphatase 2 (formerly 2A), catalytic subunit, beta isoform gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 736928 Ppp2cb protein phosphatase 2 (formerly 2A), catalytic subunit, beta isoform gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20220811 MGI 736928 Ppp2cb protein phosphatase 2 (formerly 2A), catalytic subunit, beta isoform gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 736931 Rap1b RAS related protein 1b gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15696195 736931 Rap1b RAS related protein 1b gene MP:0001454 abnormal cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:18305243 736931 Rap1b RAS related protein 1b gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:18305243 736931 Rap1b RAS related protein 1b gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:15696195 736931 Rap1b RAS related protein 1b gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:15696195 736931 Rap1b RAS related protein 1b gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:18305243 736931 Rap1b RAS related protein 1b gene MP:0002920 decreased paired-pulse facilitation IAGP N RGD:5509061 20141003 MGI PMID:18305243 736931 Rap1b RAS related protein 1b gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:18305243 736931 Rap1b RAS related protein 1b gene MP:0004494 abnormal synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:18305243 736931 Rap1b RAS related protein 1b gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:15696195 736931 Rap1b RAS related protein 1b gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:15696195 736931 Rap1b RAS related protein 1b gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15696195 736931 Rap1b RAS related protein 1b gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15696195 736931 Rap1b RAS related protein 1b gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15696195 736931 Rap1b RAS related protein 1b gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:15696195 736933 Gmeb2 glucocorticoid modulatory element binding protein 2 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20230601 MGI 736933 Gmeb2 glucocorticoid modulatory element binding protein 2 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20230601 MGI 736933 Gmeb2 glucocorticoid modulatory element binding protein 2 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 736933 Gmeb2 glucocorticoid modulatory element binding protein 2 gene MP:0005635 decreased circulating bilirubin level IEA N RGD:5509061 20230601 MGI 736933 Gmeb2 glucocorticoid modulatory element binding protein 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 736940 Hk3 hexokinase 3 gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20220519 MGI 736940 Hk3 hexokinase 3 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20220519 MGI 736940 Hk3 hexokinase 3 gene MP:0002768 small adrenal glands IEA N RGD:5509061 20220519 MGI 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0000948 nonconvulsive seizures IAGP N RGD:5509061 20141003 MGI PMID:20676103 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230601 MGI 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20211021 MGI 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:19923296 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:19923296 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0002801 abnormal long-term object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:19923296 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:20676103 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20141003 MGI PMID:20676103 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0003463 abnormal single cell response IAGP N RGD:5509061 20241017 MGI PMID:37516908 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0003466 decreased single cell response threshold IAGP N RGD:5509061 20141003 MGI PMID:20676103 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0005386 behavior/neurological phenotype IAGP N RGD:5509061 20241017 MGI PMID:37516908 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210520 MGI 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0008414 abnormal spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:19923296 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20141003 MGI PMID:19923296 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20141003 MGI PMID:20676103 736943 Kcnh3 potassium voltage-gated channel, subfamily H (eag-related), member 3 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 736945 Syt1 synaptotagmin I gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:7954835 736945 Syt1 synaptotagmin I gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15561725 736945 Syt1 synaptotagmin I gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11242035 736945 Syt1 synaptotagmin I gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12351718 736945 Syt1 synaptotagmin I gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:7954835 736945 Syt1 synaptotagmin I gene MP:0002909 abnormal adrenal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:21451027 736945 Syt1 synaptotagmin I gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21451027 736945 Syt1 synaptotagmin I gene MP:0002916 increased synaptic depression IAGP N RGD:5509061 20141003 MGI PMID:12351718 736945 Syt1 synaptotagmin I gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:17521570 736945 Syt1 synaptotagmin I gene MP:0003253 dilated bile duct IEA N RGD:5509061 20171228 MGI 736945 Syt1 synaptotagmin I gene MP:0003266 biliary cyst IEA N RGD:5509061 20170504 MGI 736945 Syt1 synaptotagmin I gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:15561725 736945 Syt1 synaptotagmin I gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:21451027 736945 Syt1 synaptotagmin I gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 736945 Syt1 synaptotagmin I gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21451027 736945 Syt1 synaptotagmin I gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:21040848 736945 Syt1 synaptotagmin I gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:11242035 736945 Syt1 synaptotagmin I gene MP:0005445 abnormal neurotransmitter secretion IAGP N RGD:5509061 20141003 MGI PMID:7954835 736945 Syt1 synaptotagmin I gene MP:0008923 thoracoschisis IEA N RGD:5509061 20171228 MGI 736945 Syt1 synaptotagmin I gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20211021 MGI 736945 Syt1 synaptotagmin I gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20171228 MGI 736945 Syt1 synaptotagmin I gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7954835 736945 Syt1 synaptotagmin I gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 736945 Syt1 synaptotagmin I gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:11242035 736945 Syt1 synaptotagmin I gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:21040848 736945 Syt1 synaptotagmin I gene MP:0013309 adrenal gland cyst IEA N RGD:5509061 20170504 MGI 736945 Syt1 synaptotagmin I gene MP:0013528 thyroid gland cyst IEA N RGD:5509061 20171228 MGI 736945 Syt1 synaptotagmin I gene MP:0013877 abnormal ductus venosus valve morphology IEA N RGD:5509061 20171228 MGI 736945 Syt1 synaptotagmin I gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20171228 MGI 736945 Syt1 synaptotagmin I gene MP:0013975 abnormal coronary sinus connection IEA N RGD:5509061 20170504 MGI 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:20682746 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:20682746 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0001425 abnormal alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:11150351 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:20682746 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0002629 hyperactivity elicited by ethanol administration IAGP N RGD:5509061 20141003 MGI PMID:11150351 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20141003 MGI PMID:18496528 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16525043 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:10103106 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9694658 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:11150351 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0009712 impaired conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:18496528 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20682746 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:14631045 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0009750 impaired behavioral response to addictive substance IAGP N RGD:5509061 20141003 MGI PMID:9694658 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:10103106 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:20682746 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0009757 impaired behavioral response to morphine IAGP N RGD:5509061 20141003 MGI PMID:18496528 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:16525043 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:18496528 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:20682746 736949 Ppp1r1b protein phosphatase 1, regulatory inhibitor subunit 1B gene MP:0009758 impaired behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:9694658 736951 Kcnc2 potassium voltage gated channel, Shaw-related subfamily, member 2 gene MP:0000243 myoclonus IAGP N RGD:5509061 20141003 MGI PMID:11124984 736951 Kcnc2 potassium voltage gated channel, Shaw-related subfamily, member 2 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:11124984 736951 Kcnc2 potassium voltage gated channel, Shaw-related subfamily, member 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:11124984 736951 Kcnc2 potassium voltage gated channel, Shaw-related subfamily, member 2 gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20141003 MGI PMID:12176162 736951 Kcnc2 potassium voltage gated channel, Shaw-related subfamily, member 2 gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:11124984 736951 Kcnc2 potassium voltage gated channel, Shaw-related subfamily, member 2 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11124984 736951 Kcnc2 potassium voltage gated channel, Shaw-related subfamily, member 2 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:11124984 736951 Kcnc2 potassium voltage gated channel, Shaw-related subfamily, member 2 gene MP:0003412 abnormal afterhyperpolarization IAGP N RGD:5509061 20141003 MGI PMID:11124984 736951 Kcnc2 potassium voltage gated channel, Shaw-related subfamily, member 2 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:11124984 736951 Kcnc2 potassium voltage gated channel, Shaw-related subfamily, member 2 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:11124984 736951 Kcnc2 potassium voltage gated channel, Shaw-related subfamily, member 2 gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:11124984 736953 Rplp1 ribosomal protein lateral stalk subunit P1 gene MP:0000477 abnormal intestine morphology IAGP N RGD:5509061 20171221 MGI PMID:24959908 736953 Rplp1 ribosomal protein lateral stalk subunit P1 gene MP:0000585 kinked tail IAGP N RGD:5509061 20171221 MGI PMID:24959908 736953 Rplp1 ribosomal protein lateral stalk subunit P1 gene MP:0000592 short tail IAGP N RGD:5509061 20171221 MGI PMID:24959908 736953 Rplp1 ribosomal protein lateral stalk subunit P1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20171221 MGI PMID:24959908 736953 Rplp1 ribosomal protein lateral stalk subunit P1 gene MP:0000706 small thymus IAGP N RGD:5509061 20171221 MGI PMID:24959908 736953 Rplp1 ribosomal protein lateral stalk subunit P1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20171221 MGI PMID:24959908 736953 Rplp1 ribosomal protein lateral stalk subunit P1 gene MP:0001925 male infertility IAGP N RGD:5509061 20171221 MGI PMID:24959908 736953 Rplp1 ribosomal protein lateral stalk subunit P1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20171221 MGI PMID:24959908 736953 Rplp1 ribosomal protein lateral stalk subunit P1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20171221 MGI PMID:24959908 736953 Rplp1 ribosomal protein lateral stalk subunit P1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20171221 MGI PMID:24959908 736953 Rplp1 ribosomal protein lateral stalk subunit P1 gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20171221 MGI PMID:24959908 736953 Rplp1 ribosomal protein lateral stalk subunit P1 gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20171221 MGI PMID:24959908 736953 Rplp1 ribosomal protein lateral stalk subunit P1 gene MP:0011239 abnormal skin coloration IAGP N RGD:5509061 20171221 MGI PMID:24959908 736953 Rplp1 ribosomal protein lateral stalk subunit P1 gene MP:0013176 abnormal tail position or orientation IAGP N RGD:5509061 20171221 MGI PMID:24959908 736956 Vtn vitronectin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:8618914 736956 Vtn vitronectin gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:15733060 736956 Vtn vitronectin gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:15733060 736956 Vtn vitronectin gene MP:0009548 abnormal platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:15733060 736957 Smad2 SMAD family member 2 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18063435 736957 Smad2 SMAD family member 2 gene MP:0000087 absent mandible IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12432092 736957 Smad2 SMAD family member 2 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12842913 736957 Smad2 SMAD family member 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:12842913 736957 Smad2 SMAD family member 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:12432092 736957 Smad2 SMAD family member 2 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:12842913 736957 Smad2 SMAD family member 2 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16382155 736957 Smad2 SMAD family member 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:11438667 736957 Smad2 SMAD family member 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0000433 microcephaly IAGP N RGD:5509061 20141003 MGI PMID:15630024 736957 Smad2 SMAD family member 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:11984875 736957 Smad2 SMAD family member 2 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0000597 delayed hepatic development IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:11438667 736957 Smad2 SMAD family member 2 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11438667 736957 Smad2 SMAD family member 2 gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:11438667 736957 Smad2 SMAD family member 2 gene MP:0000602 dilated liver sinusoidal space IAGP N RGD:5509061 20141003 MGI PMID:11438667 736957 Smad2 SMAD family member 2 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20230608 MGI PMID:16382155 736957 Smad2 SMAD family member 2 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0000857 abnormal cerebellar foliation IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:15630024 736957 Smad2 SMAD family member 2 gene MP:0000932 absent notochord IAGP N RGD:5509061 20141003 MGI PMID:12432092 736957 Smad2 SMAD family member 2 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:18809571 736957 Smad2 SMAD family member 2 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18063435 736957 Smad2 SMAD family member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18063435 736957 Smad2 SMAD family member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0001286 abnormal eye development IAGP N RGD:5509061 20160929 MGI PMID:22383895 736957 Smad2 SMAD family member 2 gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0001504 abnormal posture IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0001525 impaired balance IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9529255 736957 Smad2 SMAD family member 2 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0001683 absent mesoderm IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0001685 abnormal endoderm development IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:9529255 736957 Smad2 SMAD family member 2 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0001693 failure of primitive streak formation IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0001695 abnormal gastrulation IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:15452874 736957 Smad2 SMAD family member 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0001705 abnormal proximal-distal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0001706 abnormal left-right axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:18809571 736957 Smad2 SMAD family member 2 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:18809571 736957 Smad2 SMAD family member 2 gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:12842913 736957 Smad2 SMAD family member 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:18809571 736957 Smad2 SMAD family member 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:18809571 736957 Smad2 SMAD family member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16382155 736957 Smad2 SMAD family member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12384562 736957 Smad2 SMAD family member 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:15452874 736957 Smad2 SMAD family member 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10535967 736957 Smad2 SMAD family member 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12432092 736957 Smad2 SMAD family member 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12842913 736957 Smad2 SMAD family member 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9529255 736957 Smad2 SMAD family member 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12384562 736957 Smad2 SMAD family member 2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20141003 MGI PMID:11984875 736957 Smad2 SMAD family member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12432092 736957 Smad2 SMAD family member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12842913 736957 Smad2 SMAD family member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15452874 736957 Smad2 SMAD family member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15630024 736957 Smad2 SMAD family member 2 gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12384562 736957 Smad2 SMAD family member 2 gene MP:0002583 absent extraembryonic ectoderm IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:21990361 736957 Smad2 SMAD family member 2 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:9529255 736957 Smad2 SMAD family member 2 gene MP:0002951 small thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0003085 abnormal egg cylinder morphology IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0003087 absent allantois IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:16382155 736957 Smad2 SMAD family member 2 gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11438667 736957 Smad2 SMAD family member 2 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:15630024 736957 Smad2 SMAD family member 2 gene MP:0003312 abnormal locomotor coordination IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0003560 osteoarthritis IAGP N RGD:5509061 20141003 MGI PMID:15630024 736957 Smad2 SMAD family member 2 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:9529255 736957 Smad2 SMAD family member 2 gene MP:0003886 abnormal embryonic epiblast morphology IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0003890 abnormal embryonic-extraembryonic boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0003893 increased hepatocyte proliferation IAGP N RGD:5509061 20230608 MGI PMID:16382155 736957 Smad2 SMAD family member 2 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:18063435 736957 Smad2 SMAD family member 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20160929 MGI PMID:22383895 736957 Smad2 SMAD family member 2 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:11438667 736957 Smad2 SMAD family member 2 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:18063435 736957 Smad2 SMAD family member 2 gene MP:0004098 abnormal cerebellar granule cell morphology IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0004199 increased fetal size IAGP N RGD:5509061 20141003 MGI PMID:11438667 736957 Smad2 SMAD family member 2 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:12432092 736957 Smad2 SMAD family member 2 gene MP:0004998 decreased CNS synapse formation IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0005023 abnormal wound healing IAGP N RGD:5509061 20141003 MGI PMID:21990361 736957 Smad2 SMAD family member 2 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0005030 absent amnion IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0005032 abnormal ectoplacental cone morphology IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16382155 736957 Smad2 SMAD family member 2 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20141003 MGI PMID:15630024 736957 Smad2 SMAD family member 2 gene MP:0005157 holoprosencephaly IAGP N RGD:5509061 20160929 MGI PMID:22383895 736957 Smad2 SMAD family member 2 gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0005163 cyclopia IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:12842913 736957 Smad2 SMAD family member 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9529255 736957 Smad2 SMAD family member 2 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:18809571 736957 Smad2 SMAD family member 2 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:11984875 736957 Smad2 SMAD family member 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16382155 736957 Smad2 SMAD family member 2 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16382155 736957 Smad2 SMAD family member 2 gene MP:0006108 abnormal hindbrain development IAGP N RGD:5509061 20141003 MGI PMID:15630024 736957 Smad2 SMAD family member 2 gene MP:0006207 embryonic lethality during organogenesis IAGP N RGD:5509061 20141003 MGI PMID:12842913 736957 Smad2 SMAD family member 2 gene MP:0006290 proboscis IAGP N RGD:5509061 20160929 MGI PMID:22383895 736957 Smad2 SMAD family member 2 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0008572 abnormal Purkinje cell dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0008789 abnormal olfactory epithelium morphology IAGP N RGD:5509061 20160929 MGI PMID:22383895 736957 Smad2 SMAD family member 2 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16382155 736957 Smad2 SMAD family member 2 gene MP:0008926 abnormal anterior definitive endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:12842913 736957 Smad2 SMAD family member 2 gene MP:0009331 absent primitive node IAGP N RGD:5509061 20141003 MGI PMID:9529255 736957 Smad2 SMAD family member 2 gene MP:0009373 abnormal cumulus expansion IAGP N RGD:5509061 20141003 MGI PMID:18809571 736957 Smad2 SMAD family member 2 gene MP:0009593 absent chorion IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:12432092 736957 Smad2 SMAD family member 2 gene MP:0009977 abnormal cerebellar granule cell migration IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0009992 abnormal cerebellum vermis lobule IX morphology IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0009997 abnormal cerebellum vermis lobule X morphology IAGP N RGD:5509061 20141003 MGI PMID:21464123 736957 Smad2 SMAD family member 2 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11438667 736957 Smad2 SMAD family member 2 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20230608 MGI PMID:16382155 736957 Smad2 SMAD family member 2 gene MP:0010117 abnormal lateral plate mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:18063435 736957 Smad2 SMAD family member 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15630024 736957 Smad2 SMAD family member 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12432092 736957 Smad2 SMAD family member 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15452874 736957 Smad2 SMAD family member 2 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10535967 736957 Smad2 SMAD family member 2 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12432092 736957 Smad2 SMAD family member 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15452874 736957 Smad2 SMAD family member 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9529255 736957 Smad2 SMAD family member 2 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15630024 736957 Smad2 SMAD family member 2 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11438667 736957 Smad2 SMAD family member 2 gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18809571 736957 Smad2 SMAD family member 2 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0011197 abnormal proamniotic cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0011733 fused somites IAGP N RGD:5509061 20141003 MGI PMID:12842913 736957 Smad2 SMAD family member 2 gene MP:0012083 absent foregut IAGP N RGD:5509061 20141003 MGI PMID:12432092 736957 Smad2 SMAD family member 2 gene MP:0012083 absent foregut IAGP N RGD:5509061 20141003 MGI PMID:12842913 736957 Smad2 SMAD family member 2 gene MP:0012084 truncated foregut IAGP N RGD:5509061 20141003 MGI PMID:12842913 736957 Smad2 SMAD family member 2 gene MP:0012087 absent midbrain IAGP N RGD:5509061 20141003 MGI PMID:12842913 736957 Smad2 SMAD family member 2 gene MP:0012136 absent forebrain IAGP N RGD:5509061 20141003 MGI PMID:12842913 736957 Smad2 SMAD family member 2 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:12432092 736957 Smad2 SMAD family member 2 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:12842913 736957 Smad2 SMAD family member 2 gene MP:0012157 rostral body truncation IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0012170 absent optic placodes IAGP N RGD:5509061 20141003 MGI PMID:12432092 736957 Smad2 SMAD family member 2 gene MP:0012193 increased keratinocyte migration IAGP N RGD:5509061 20141204 MGI PMID:21990361 736957 Smad2 SMAD family member 2 gene MP:0012245 abnormal hepatoblast migration IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0012246 abnormal hepatic cord morphology IAGP N RGD:5509061 20141003 MGI PMID:11438667 736957 Smad2 SMAD family member 2 gene MP:0012501 abnormal pericardial cavity morphology IAGP N RGD:5509061 20141003 MGI PMID:15183723 736957 Smad2 SMAD family member 2 gene MP:0012685 abnormal primitive streak elongation IAGP N RGD:5509061 20141003 MGI PMID:9655392 736957 Smad2 SMAD family member 2 gene MP:0012724 absent head fold IAGP N RGD:5509061 20141003 MGI PMID:9689088 736957 Smad2 SMAD family member 2 gene MP:0013207 absent endoderm IAGP N RGD:5509061 20141003 MGI PMID:9529255 736957 Smad2 SMAD family member 2 gene MP:0013216 absent ectoderm IAGP N RGD:5509061 20141003 MGI PMID:9529255 736957 Smad2 SMAD family member 2 gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:12384562 736957 Smad2 SMAD family member 2 gene MP:0031020 premature ovarian failure IAGP N RGD:5509061 20200130 MGI PMID:18809571 736957 Smad2 SMAD family member 2 gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:18809571 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:9882500 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:17301292 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:9882500 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:24089200 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:9882500 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:9882500 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17301292 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:24089200 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0002686 globozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17301292 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:12606345 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:24089200 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:9882500 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220317 MGI PMID:17301292 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0004543 abnormal sperm physiology IAGP N RGD:5509061 20141003 MGI PMID:12606345 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:9882500 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20141003 MGI PMID:9882500 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20181227 MGI 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:24089200 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17301292 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17301292 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17301292 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:12606345 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:17301292 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0009236 pinhead sperm IAGP N RGD:5509061 20141003 MGI PMID:17301292 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:24089200 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:12606345 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:17301292 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0009832 abnormal sperm mitochondrial sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:24089200 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0009833 absent sperm mitochondrial sheath IAGP N RGD:5509061 20141003 MGI PMID:17301292 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0009836 abnormal sperm principal piece morphology IAGP N RGD:5509061 20141003 MGI PMID:17301292 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0009839 multiflagellated sperm IAGP N RGD:5509061 20141003 MGI PMID:12606345 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0014468 disorganized sperm mitochondrial sheath IAGP N RGD:5509061 20240613 MGI PMID:17301292 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0030590 abnormal sperm fibrous sheath morphology IAGP N RGD:5509061 20180621 MGI PMID:17301292 736959 Ppp1cc protein phosphatase 1 catalytic subunit gamma gene MP:0031356 abnormal outer dense fiber morphology IAGP N RGD:5509061 20220317 MGI PMID:17301292 736960 Prkar2a protein kinase, cAMP dependent regulatory, type II alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9380760 736965 Mapk4 mitogen-activated protein kinase 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150430 MGI PMID:20956558 736965 Mapk4 mitogen-activated protein kinase 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20150430 MGI PMID:20956558 736965 Mapk4 mitogen-activated protein kinase 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150430 MGI PMID:20956558 736965 Mapk4 mitogen-activated protein kinase 4 gene MP:0010810 increased type II pneumocyte number IAGP N RGD:5509061 20150430 MGI PMID:20956558 736965 Mapk4 mitogen-activated protein kinase 4 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20150430 MGI PMID:20956558 736965 Mapk4 mitogen-activated protein kinase 4 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20150430 MGI PMID:20956558 736967 Slco2a1 solute carrier organic anion transporter family, member 2a1 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:20083684 736967 Slco2a1 solute carrier organic anion transporter family, member 2a1 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:20083684 736967 Slco2a1 solute carrier organic anion transporter family, member 2a1 gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:20083684 736967 Slco2a1 solute carrier organic anion transporter family, member 2a1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:20083684 736967 Slco2a1 solute carrier organic anion transporter family, member 2a1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20083684 736967 Slco2a1 solute carrier organic anion transporter family, member 2a1 gene MP:0009811 abnormal prostaglandin level IAGP N RGD:5509061 20141003 MGI PMID:20083684 736967 Slco2a1 solute carrier organic anion transporter family, member 2a1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20083684 736967 Slco2a1 solute carrier organic anion transporter family, member 2a1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20083684 736971 Rgs6 regulator of G-protein signaling 6 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:20884879 736971 Rgs6 regulator of G-protein signaling 6 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:20864673 736971 Rgs6 regulator of G-protein signaling 6 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:20884879 736971 Rgs6 regulator of G-protein signaling 6 gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:20864673 736971 Rgs6 regulator of G-protein signaling 6 gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:20884879 736974 Gpr119 G-protein coupled receptor 119 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180607 MGI PMID:19282326 736974 Gpr119 G-protein coupled receptor 119 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20180607 MGI PMID:19282326 736975 Kcnmb1 potassium large conductance calcium-activated channel, subfamily M, beta member 1 gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:11057658 736975 Kcnmb1 potassium large conductance calcium-activated channel, subfamily M, beta member 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:11057658 736975 Kcnmb1 potassium large conductance calcium-activated channel, subfamily M, beta member 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11057658 736975 Kcnmb1 potassium large conductance calcium-activated channel, subfamily M, beta member 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:11090555 736975 Kcnmb1 potassium large conductance calcium-activated channel, subfamily M, beta member 1 gene MP:0002847 abnormal renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:12620927 736975 Kcnmb1 potassium large conductance calcium-activated channel, subfamily M, beta member 1 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:11090555 736975 Kcnmb1 potassium large conductance calcium-activated channel, subfamily M, beta member 1 gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:23255603 736975 Kcnmb1 potassium large conductance calcium-activated channel, subfamily M, beta member 1 gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11090555 736975 Kcnmb1 potassium large conductance calcium-activated channel, subfamily M, beta member 1 gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11731577 736978 Bnip1 BCL2/adenovirus E1B interacting protein 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 736978 Bnip1 BCL2/adenovirus E1B interacting protein 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 736978 Bnip1 BCL2/adenovirus E1B interacting protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 736979 Capn10 calpain 10 gene MP:0001260 increased body weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 736979 Capn10 calpain 10 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 736979 Capn10 calpain 10 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20211021 MGI 736979 Capn10 calpain 10 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20180621 MGI PMID:20388922 736979 Capn10 calpain 10 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:15044459 736979 Capn10 calpain 10 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20180621 MGI PMID:20388922 736979 Capn10 calpain 10 gene MP:0002764 short tibia IEA N RGD:5509061 20200514 MGI 736979 Capn10 calpain 10 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 736979 Capn10 calpain 10 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 736979 Capn10 calpain 10 gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 736979 Capn10 calpain 10 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 736979 Capn10 calpain 10 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20180621 MGI PMID:20388922 736979 Capn10 calpain 10 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20211021 MGI 736979 Capn10 calpain 10 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 736979 Capn10 calpain 10 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20180621 MGI PMID:20388922 736979 Capn10 calpain 10 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20180621 MGI PMID:20388922 736979 Capn10 calpain 10 gene MP:0008908 increased total fat pad weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 736979 Capn10 calpain 10 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 736979 Capn10 calpain 10 gene MP:0009292 increased inguinal fat pad weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 736979 Capn10 calpain 10 gene MP:0009298 increased mesenteric fat pad weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 736979 Capn10 calpain 10 gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20180621 MGI PMID:20388922 736981 Capn1 calpain 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:21791606 736981 Capn1 calpain 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:21791606 736981 Capn1 calpain 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21791606 736981 Capn1 calpain 1 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:21791606 736981 Capn1 calpain 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21791606 736981 Capn1 calpain 1 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:11238954 736981 Capn1 calpain 1 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:21415394 736981 Capn1 calpain 1 gene MP:0004266 pale placenta IAGP N RGD:5509061 20141003 MGI PMID:21791606 736981 Capn1 calpain 1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:11238954 736981 Capn1 calpain 1 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:22665935 736981 Capn1 calpain 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21415394 736981 Capn1 calpain 1 gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20141003 MGI PMID:11238954 736981 Capn1 calpain 1 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:11238954 736981 Capn1 calpain 1 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:21791606 736981 Capn1 calpain 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21791606 736982 Abcf1 ATP-binding cassette, sub-family F member 1 gene MP:0013292 embryonic lethality prior to organogenesis IAGP N RGD:5509061 20180215 MGI PMID:28542262 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:16407979 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0000792 abnormal cortical marginal zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16407979 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0000794 abnormal parietal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:16407979 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0000798 abnormal frontal lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:16407979 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20141003 MGI PMID:16407979 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:16407979 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16407979 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:14689444 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:16407979 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16407979 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0002196 absent corpus callosum IAGP N RGD:5509061 20141003 MGI PMID:16407979 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:14689444 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:16407979 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0004227 increased cellular sensitivity to ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:17121854 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17121854 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0005623 abnormal meninges morphology IAGP N RGD:5509061 20141003 MGI PMID:16407979 736983 Apbb1 amyloid beta precursor protein binding family B member 1 gene MP:0009026 abnormal brain pia mater morphology IAGP N RGD:5509061 20141003 MGI PMID:16407979 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0000692 small spleen IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0001284 absent vibrissae IEA N RGD:5509061 20240523 MGI 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210128 MGI 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0003717 pallor IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0010394 decreased QRS amplitude IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0010499 abnormal ventricle myocardium morphology IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20211104 MGI PMID:34622152 736985 Srsf5 serine and arginine-rich splicing factor 5 gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231221 MGI PMID:34622152 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:8107803 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0000819 abnormal olfactory bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:8274281 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20141003 MGI PMID:8274281 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0000952 abnormal CNS glial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17682066 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:8274281 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:8107803 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:14973228 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0001899 absent long-term depression IAGP N RGD:5509061 20141003 MGI PMID:14973228 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20200123 MGI PMID:27103522 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0002184 abnormal innervation IAGP N RGD:5509061 20240523 MGI PMID:25007825 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:8107803 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:8274281 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:9482932 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0002983 increased retina ganglion cell number IAGP N RGD:5509061 20200123 MGI PMID:27103522 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:9011400 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200123 MGI PMID:27103522 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:9482932 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:9011400 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:9011400 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0006149 decreased visual acuity IAGP N RGD:5509061 20200123 MGI PMID:27103522 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0006309 decreased retina ganglion cell number IAGP N RGD:5509061 20200123 MGI PMID:27103522 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0008267 abnormal hippocampus CA3 region morphology IAGP N RGD:5509061 20141003 MGI PMID:9482932 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:8274281 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0008508 thick retina ganglion layer IAGP N RGD:5509061 20200123 MGI PMID:27103522 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:27103522 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20200123 MGI PMID:27103522 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0008519 thin retina outer plexiform layer IAGP N RGD:5509061 20200123 MGI PMID:27103522 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17682066 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8692830 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0011963 abnormal total retina thickness IAGP N RGD:5509061 20200123 MGI PMID:27103522 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0014265 thick retina inner plexiform layer IAGP N RGD:5509061 20230706 MGI PMID:27103522 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0020468 abnormal circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:11399310 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:11399310 736988 Ncam1 neural cell adhesion molecule 1 gene MP:0020473 abnormal circadian behavior phase IAGP N RGD:5509061 20171012 MGI PMID:11399310 736991 Oxr1 oxidation resistance 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20211021 MGI 736991 Oxr1 oxidation resistance 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20161020 MGI PMID:26668325 736991 Oxr1 oxidation resistance 1 gene MP:0001393 ataxia IAGP N RGD:5509061 20210617 MGI PMID:33340069 736991 Oxr1 oxidation resistance 1 gene MP:0002083 premature death IAGP N RGD:5509061 20161020 MGI PMID:26668325 736991 Oxr1 oxidation resistance 1 gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20161020 MGI PMID:26668325 736991 Oxr1 oxidation resistance 1 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20201022 MGI 736991 Oxr1 oxidation resistance 1 gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20161020 MGI PMID:26668325 736991 Oxr1 oxidation resistance 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20210617 MGI PMID:33340069 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0000473 abnormal stomach glandular epithelium morphology IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11869681 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11869681 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0001862 interstitial pneumonia IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0002083 premature death IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0002344 abnormal lymph node B cell domain morphology IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0002392 abnormal Peyer's patch T cell area morphology IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11869681 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:11869681 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11869681 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0002816 colitis IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0004137 abnormal gastric surface mucous cell morphology IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11869681 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11869681 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0008174 decreased follicular B cell number IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0008479 decreased spleen white pulp amount IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0011339 abnormal glomerular mesangium morphology IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0012762 abnormal alpha-beta T cell morphology IAGP N RGD:5509061 20161013 MGI PMID:17086554 736994 Wipf1 WAS/WASL interacting protein family, member 1 gene MP:0013693 abnormal hemopoiesis IAGP N RGD:5509061 20161013 MGI PMID:17086554 736998 Lhx3 LIM homeobox protein 3 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9865699 736998 Lhx3 LIM homeobox protein 3 gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:18054242 736998 Lhx3 LIM homeobox protein 3 gene MP:0001070 abnormal abducens nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9865699 736998 Lhx3 LIM homeobox protein 3 gene MP:0001076 abnormal hypoglossal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9865699 736998 Lhx3 LIM homeobox protein 3 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9865699 736998 Lhx3 LIM homeobox protein 3 gene MP:0001120 abnormal uterus morphology IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18054242 736998 Lhx3 LIM homeobox protein 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0002774 small prostate gland IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0002779 abnormal sex gland secretion IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0003503 decreased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0003572 abnormal uterus development IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0003816 abnormal pituitary gland development IAGP N RGD:5509061 20141218 MGI PMID:8638120 736998 Lhx3 LIM homeobox protein 3 gene MP:0003965 abnormal pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0003993 abnormal ventral spinal root morphology IAGP N RGD:5509061 20141003 MGI PMID:18054242 736998 Lhx3 LIM homeobox protein 3 gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0005128 decreased adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0005128 decreased adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:8638120 736998 Lhx3 LIM homeobox protein 3 gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:8638120 736998 Lhx3 LIM homeobox protein 3 gene MP:0005134 decreased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:8638120 736998 Lhx3 LIM homeobox protein 3 gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:8638120 736998 Lhx3 LIM homeobox protein 3 gene MP:0005138 decreased prolactin level IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0008299 adrenal cortical hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8638120 736998 Lhx3 LIM homeobox protein 3 gene MP:0008320 absent adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:16859901 736998 Lhx3 LIM homeobox protein 3 gene MP:0008320 absent adenohypophysis IAGP N RGD:5509061 20141003 MGI PMID:9865699 736998 Lhx3 LIM homeobox protein 3 gene MP:0008320 absent adenohypophysis IAGP N RGD:5509061 20141218 MGI PMID:8638120 736998 Lhx3 LIM homeobox protein 3 gene MP:0008327 abnormal corticotroph morphology IAGP N RGD:5509061 20141003 MGI PMID:8638120 736998 Lhx3 LIM homeobox protein 3 gene MP:0008330 absent somatotrophs IAGP N RGD:5509061 20141003 MGI PMID:8638120 736998 Lhx3 LIM homeobox protein 3 gene MP:0008332 decreased lactotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0008333 absent lactotrophs IAGP N RGD:5509061 20141003 MGI PMID:8638120 736998 Lhx3 LIM homeobox protein 3 gene MP:0008335 decreased gonadotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0008335 decreased gonadotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:8638120 736998 Lhx3 LIM homeobox protein 3 gene MP:0008339 absent thyrotrophs IAGP N RGD:5509061 20141003 MGI PMID:8638120 736998 Lhx3 LIM homeobox protein 3 gene MP:0008365 adenohypophysis hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0008367 absent pituitary intermediate lobe IAGP N RGD:5509061 20141003 MGI PMID:9865699 736998 Lhx3 LIM homeobox protein 3 gene MP:0008367 absent pituitary intermediate lobe IAGP N RGD:5509061 20141218 MGI PMID:8638120 736998 Lhx3 LIM homeobox protein 3 gene MP:0008368 small pituitary intermediate lobe IAGP N RGD:5509061 20141003 MGI PMID:16859901 736998 Lhx3 LIM homeobox protein 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0009205 abnormal internal male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9865699 736998 Lhx3 LIM homeobox protein 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21149718 736998 Lhx3 LIM homeobox protein 3 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8638120 736998 Lhx3 LIM homeobox protein 3 gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:16859901 736998 Lhx3 LIM homeobox protein 3 gene MP:0013351 abnormal Rathke's pouch development IAGP N RGD:5509061 20141218 MGI PMID:8638120 736998 Lhx3 LIM homeobox protein 3 gene MP:0013352 abnormal Rathke's pouch apoptosis IAGP N RGD:5509061 20141218 MGI PMID:16859901 737000 Rnf40 ring finger protein 40 gene MP:0004149 increased bone strength IAGP N RGD:5509061 20211028 MGI PMID:30321325 737000 Rnf40 ring finger protein 40 gene MP:0008539 decreased susceptibility to induced colitis IAGP N RGD:5509061 20211028 MGI PMID:30321325 737000 Rnf40 ring finger protein 40 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737000 Rnf40 ring finger protein 40 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 737001 Rps27 ribosomal protein S27 gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20241010 MGI 737001 Rps27 ribosomal protein S27 gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20241010 MGI 737001 Rps27 ribosomal protein S27 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240808 MGI PMID:37306301 737001 Rps27 ribosomal protein S27 gene MP:0002582 disorganized extraembryonic tissue IEA N RGD:5509061 20241010 MGI 737001 Rps27 ribosomal protein S27 gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20241010 MGI 737001 Rps27 ribosomal protein S27 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20241010 MGI 737001 Rps27 ribosomal protein S27 gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 737001 Rps27 ribosomal protein S27 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20240808 MGI PMID:37306301 737001 Rps27 ribosomal protein S27 gene MP:0014259 embryonic lethality prior to organogenesis, complete penetrance IAGP N RGD:5509061 20240808 MGI PMID:37306301 737002 Cntf ciliary neurotrophic factor gene MP:0000136 abnormal microglial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:8361533 737002 Cntf ciliary neurotrophic factor gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:8361533 737002 Cntf ciliary neurotrophic factor gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11085886 737002 Cntf ciliary neurotrophic factor gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8361533 737002 Cntf ciliary neurotrophic factor gene MP:0000938 motor neuron degeneration IAGP N RGD:5509061 20141003 MGI PMID:8361533 737002 Cntf ciliary neurotrophic factor gene MP:0000939 decreased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:8361533 737002 Cntf ciliary neurotrophic factor gene MP:0000954 decreased oligodendrocyte progenitor number IAGP N RGD:5509061 20141003 MGI PMID:12042814 737002 Cntf ciliary neurotrophic factor gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:22764235 737002 Cntf ciliary neurotrophic factor gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:19906980 737002 Cntf ciliary neurotrophic factor gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:12042814 737002 Cntf ciliary neurotrophic factor gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:12042814 737002 Cntf ciliary neurotrophic factor gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:18305256 737002 Cntf ciliary neurotrophic factor gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:12843240 737002 Cntf ciliary neurotrophic factor gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:19906980 737002 Cntf ciliary neurotrophic factor gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:12042814 737002 Cntf ciliary neurotrophic factor gene MP:0006060 increased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:22764235 737002 Cntf ciliary neurotrophic factor gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:12843240 737002 Cntf ciliary neurotrophic factor gene MP:0009967 abnormal neuron proliferation IAGP N RGD:5509061 20141003 MGI PMID:18305256 737002 Cntf ciliary neurotrophic factor gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:8361533 737002 Cntf ciliary neurotrophic factor gene MP:0010205 abnormal oligodendrocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:12042814 737007 Atp12a ATPase, H+/K+ transporting, nongastric, alpha polypeptide gene MP:0003866 abnormal defecation IAGP N RGD:5509061 20141003 MGI PMID:9449685 737007 Atp12a ATPase, H+/K+ transporting, nongastric, alpha polypeptide gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:9449685 737007 Atp12a ATPase, H+/K+ transporting, nongastric, alpha polypeptide gene MP:0005619 increased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:9449685 737007 Atp12a ATPase, H+/K+ transporting, nongastric, alpha polypeptide gene MP:0005628 decreased circulating potassium level IAGP N RGD:5509061 20141003 MGI PMID:9449685 737007 Atp12a ATPase, H+/K+ transporting, nongastric, alpha polypeptide gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:9449685 737009 Cds1 CDP-diacylglycerol synthase 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 737009 Cds1 CDP-diacylglycerol synthase 1 gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 737009 Cds1 CDP-diacylglycerol synthase 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210826 MGI 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000040 absent middle ear ossicles IAGP N RGD:5509061 20171005 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000091 short premaxilla IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000103 nasal bone hypoplasia IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000108 midline facial cleft IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:17050624 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9500550 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:17050624 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000269 abnormal heart looping IAGP N RGD:5509061 20141003 MGI PMID:9500550 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:17050624 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17050624 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000279 ventricular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20211021 MGI PMID:29016838 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000847 abnormal metencephalon morphology IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0000934 abnormal telencephalon development IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20211021 MGI PMID:29016838 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001680 abnormal mesoderm development IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001700 abnormal embryo turning IAGP N RGD:5509061 20141003 MGI PMID:9500550 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001712 abnormal placenta development IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001713 decreased trophoblast giant cell number IAGP N RGD:5509061 20141003 MGI PMID:9500551 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:9500551 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:9500550 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001724 abnormal extraembryonic endoderm formation IAGP N RGD:5509061 20141003 MGI PMID:15073150 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001727 abnormal embryo implantation IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9500551 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20211021 MGI PMID:29016838 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:9500551 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9500550 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20882677 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9500550 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9500551 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20211021 MGI PMID:29016838 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002584 small ectoplacental cone IAGP N RGD:5509061 20141003 MGI PMID:9500551 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20211021 MGI PMID:29016838 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002824 abnormal chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:9500550 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002836 abnormal chorion morphology IAGP N RGD:5509061 20141003 MGI PMID:9500550 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0002884 abnormal pharyngeal arch morphology IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:17050624 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0003649 decreased heart right ventricle size IAGP N RGD:5509061 20211021 MGI PMID:29016838 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0003843 abnormal sagittal suture morphology IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17050624 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0003935 abnormal craniofacial development IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9500550 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20170824 MGI PMID:27783597 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15073150 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004377 small frontal bone IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004385 interparietal bone hypoplasia IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004455 pterygoid bone hypoplasia IAGP N RGD:5509061 20171005 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004461 basisphenoid bone hypoplasia IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004470 small nasal bone IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004473 absent nasal bone IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004556 enlarged allantois IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004869 frontal bone hypoplasia IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004871 premaxilla hypoplasia IAGP N RGD:5509061 20171005 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004872 absent nasal septum IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004899 absent temporal bone squamous part IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004915 abnormal Reichert's cartilage morphology IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0005029 abnormal amnion morphology IAGP N RGD:5509061 20141003 MGI PMID:9500550 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9500551 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0005244 hemopericardium IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20170824 MGI PMID:27783597 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0005650 abnormal limb bud morphology IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:17050624 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20211021 MGI PMID:29016838 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0006372 impaired placental function IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0008959 abnormal spongiotrophoblast cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0009653 abnormal palate development IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0009655 abnormal secondary palate development IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0009895 decreased palatine bone horizontal plate size IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0009897 decreased maxillary shelf size IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0010395 abnormal pharyngeal arch development IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20211021 MGI PMID:29016838 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0010432 common ventricle IAGP N RGD:5509061 20170824 MGI PMID:27783597 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0010498 abnormal interventricular septum muscular part morphology IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0010580 decreased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0010831 lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0010940 abnormal maxillary prominence morphology IAGP N RGD:5509061 20141120 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15073150 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20170824 MGI PMID:27783597 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15073150 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15576406 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20882677 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9500550 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9500551 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20211021 MGI PMID:29016838 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17050624 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20737509 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20211021 MGI PMID:29016838 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011203 abnormal parietal yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:9500551 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0011205 excessive folding of visceral yolk sac IAGP N RGD:5509061 20141003 MGI PMID:9500550 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0012270 cardiac edema IAGP N RGD:5509061 20211021 MGI PMID:29016838 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0012515 abnormal heart apex morphology IAGP N RGD:5509061 20211021 MGI PMID:29016838 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0012556 increased cell death IAGP N RGD:5509061 20211021 MGI PMID:29016838 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0013933 short Meckel's cartilage IAGP N RGD:5509061 20170810 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0030112 zygomatic bone hypoplasia IAGP N RGD:5509061 20171005 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0030122 temporal bone squamous part hypoplasia IAGP N RGD:5509061 20171005 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0030124 middle ear ossicle hypoplasia IAGP N RGD:5509061 20171005 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0030989 decreased spongiotrophoblast cell number IAGP N RGD:5509061 20191219 MGI PMID:23911935 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0031443 abnormal tongue position IAGP N RGD:5509061 20221027 MGI PMID:25053435 737011 Hand1 heart and neural crest derivatives expressed 1 gene MP:0031525 thin left ventricle myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:29016838 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:20500056 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0000273 overriding aortic valve IEA N RGD:5509061 20141003 MGI 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0000276 heart right ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160929 MGI PMID:27534441 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20181227 MGI 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20141003 MGI 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0002625 heart left ventricle hypertrophy IEA N RGD:5509061 20141003 MGI 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0002639 micrognathia IEA N RGD:5509061 20141003 MGI 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0004113 abnormal aortic arch morphology IEA N RGD:5509061 20141003 MGI 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0004158 right aortic arch IEA N RGD:5509061 20141003 MGI 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0009887 abnormal palatal shelf fusion at midline IAGP N RGD:5509061 20141003 MGI PMID:20500056 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0010053 decreased grip strength IEA N RGD:5509061 20211021 MGI 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0010418 perimembraneous ventricular septal defect IEA N RGD:5509061 20141003 MGI 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0011667 double outlet right ventricle with atrioventricular septal defect IEA N RGD:5509061 20141003 MGI 737012 Ap2b1 adaptor-related protein complex 2, beta 1 subunit gene MP:0011668 double outlet right ventricle, Taussig bing type IEA N RGD:5509061 20141003 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15208271 737014 Tlr4 toll-like receptor 4 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17519423 737014 Tlr4 toll-like receptor 4 gene MP:0000316 cellular necrosis IEA N RGD:5509061 20160915 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0000371 diluted coat color IEA N RGD:5509061 20111116 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20181227 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20160324 MGI PMID:25172014 737014 Tlr4 toll-like receptor 4 gene MP:0000607 abnormal hepatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16118350 737014 Tlr4 toll-like receptor 4 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:15795240 737014 Tlr4 toll-like receptor 4 gene MP:0001005 abnormal retina rod cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18981228 737014 Tlr4 toll-like receptor 4 gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20210520 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17519423 737014 Tlr4 toll-like receptor 4 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:15208271 737014 Tlr4 toll-like receptor 4 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20141003 MGI PMID:17403033 737014 Tlr4 toll-like receptor 4 gene MP:0001433 polyphagia IAGP N RGD:5509061 20160324 MGI PMID:25172014 737014 Tlr4 toll-like receptor 4 gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:17403033 737014 Tlr4 toll-like receptor 4 gene MP:0001547 abnormal lipid level IAGP N RGD:5509061 20141003 MGI PMID:17519423 737014 Tlr4 toll-like receptor 4 gene MP:0001570 abnormal circulating enzyme level IAGP N RGD:5509061 20141003 MGI PMID:15996225 737014 Tlr4 toll-like receptor 4 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:16118350 737014 Tlr4 toll-like receptor 4 gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:18802464 737014 Tlr4 toll-like receptor 4 gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15039466 737014 Tlr4 toll-like receptor 4 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16322526 737014 Tlr4 toll-like receptor 4 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:16118350 737014 Tlr4 toll-like receptor 4 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:15731076 737014 Tlr4 toll-like receptor 4 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:15809417 737014 Tlr4 toll-like receptor 4 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17519423 737014 Tlr4 toll-like receptor 4 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:17053835 737014 Tlr4 toll-like receptor 4 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:15731076 737014 Tlr4 toll-like receptor 4 gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:17626835 737014 Tlr4 toll-like receptor 4 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14699006 737014 Tlr4 toll-like receptor 4 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:17053835 737014 Tlr4 toll-like receptor 4 gene MP:0002271 abnormal pulmonary alveolar duct morphology IAGP N RGD:5509061 20141003 MGI PMID:17053835 737014 Tlr4 toll-like receptor 4 gene MP:0002276 abnormal lung interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:16244651 737014 Tlr4 toll-like receptor 4 gene MP:0002319 hyperoxia IAGP N RGD:5509061 20141003 MGI PMID:16244651 737014 Tlr4 toll-like receptor 4 gene MP:0002334 abnormal airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:17626835 737014 Tlr4 toll-like receptor 4 gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15039466 737014 Tlr4 toll-like receptor 4 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11294571 737014 Tlr4 toll-like receptor 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:10201887 737014 Tlr4 toll-like receptor 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:1086804 737014 Tlr4 toll-like receptor 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:11489994 737014 Tlr4 toll-like receptor 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:14742522 737014 Tlr4 toll-like receptor 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15039311 737014 Tlr4 toll-like receptor 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15039466 737014 Tlr4 toll-like receptor 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:15826931 737014 Tlr4 toll-like receptor 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:16891416 737014 Tlr4 toll-like receptor 4 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9851930 737014 Tlr4 toll-like receptor 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:10549626 737014 Tlr4 toll-like receptor 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15039311 737014 Tlr4 toll-like receptor 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:15039466 737014 Tlr4 toll-like receptor 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16148141 737014 Tlr4 toll-like receptor 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17118979 737014 Tlr4 toll-like receptor 4 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17353199 737014 Tlr4 toll-like receptor 4 gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:15039466 737014 Tlr4 toll-like receptor 4 gene MP:0002498 abnormal acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:15826931 737014 Tlr4 toll-like receptor 4 gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:18974879 737014 Tlr4 toll-like receptor 4 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18974879 737014 Tlr4 toll-like receptor 4 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17519423 737014 Tlr4 toll-like receptor 4 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:12727921 737014 Tlr4 toll-like receptor 4 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:15826931 737014 Tlr4 toll-like receptor 4 gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:15996225 737014 Tlr4 toll-like receptor 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:15039311 737014 Tlr4 toll-like receptor 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17118979 737014 Tlr4 toll-like receptor 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:17314284 737014 Tlr4 toll-like receptor 4 gene MP:0003204 decreased neuron apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17693552 737014 Tlr4 toll-like receptor 4 gene MP:0003209 abnormal pulmonary elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17053835 737014 Tlr4 toll-like receptor 4 gene MP:0003293 rectal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:8982246 737014 Tlr4 toll-like receptor 4 gene MP:0003304 large intestinal inflammation IAGP N RGD:5509061 20160324 MGI PMID:25172014 737014 Tlr4 toll-like receptor 4 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:19218085 737014 Tlr4 toll-like receptor 4 gene MP:0003449 abnormal intestinal goblet cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22796522 737014 Tlr4 toll-like receptor 4 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:17693552 737014 Tlr4 toll-like receptor 4 gene MP:0003690 abnormal glial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15809417 737014 Tlr4 toll-like receptor 4 gene MP:0003691 abnormal microglial cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15879150 737014 Tlr4 toll-like receptor 4 gene MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:15684036 737014 Tlr4 toll-like receptor 4 gene MP:0003727 abnormal retina layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18981228 737014 Tlr4 toll-like receptor 4 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:15208271 737014 Tlr4 toll-like receptor 4 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:15731076 737014 Tlr4 toll-like receptor 4 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:17403033 737014 Tlr4 toll-like receptor 4 gene MP:0003881 abnormal nephron morphology IAGP N RGD:5509061 20141003 MGI PMID:18974879 737014 Tlr4 toll-like receptor 4 gene MP:0003948 abnormal gas homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17519423 737014 Tlr4 toll-like receptor 4 gene MP:0004042 decreased susceptibility to kidney reperfusion injury IAGP N RGD:5509061 20141003 MGI PMID:18974879 737014 Tlr4 toll-like receptor 4 gene MP:0004154 renal tubular necrosis IAGP N RGD:5509061 20141003 MGI PMID:18974879 737014 Tlr4 toll-like receptor 4 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:15967420 737014 Tlr4 toll-like receptor 4 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:18054559 737014 Tlr4 toll-like receptor 4 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:20526283 737014 Tlr4 toll-like receptor 4 gene MP:0004774 abnormal bile salt level IAGP N RGD:5509061 20141003 MGI PMID:22796522 737014 Tlr4 toll-like receptor 4 gene MP:0004882 enlarged lung IAGP N RGD:5509061 20141003 MGI PMID:17053835 737014 Tlr4 toll-like receptor 4 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:14699006 737014 Tlr4 toll-like receptor 4 gene MP:0004892 increased adiponectin level IAGP N RGD:5509061 20141003 MGI PMID:17519423 737014 Tlr4 toll-like receptor 4 gene MP:0004906 enlarged uterus IEA N RGD:5509061 20181227 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0004951 abnormal spleen weight IAGP N RGD:5509061 20141003 MGI PMID:8982246 737014 Tlr4 toll-like receptor 4 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:8982246 737014 Tlr4 toll-like receptor 4 gene MP:0004977 increased B-1 B cell number IAGP N RGD:5509061 20141003 MGI PMID:16703567 737014 Tlr4 toll-like receptor 4 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16703567 737014 Tlr4 toll-like receptor 4 gene MP:0005042 abnormal level of surface class II molecules IAGP N RGD:5509061 20141003 MGI PMID:10549626 737014 Tlr4 toll-like receptor 4 gene MP:0005087 decreased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:8982246 737014 Tlr4 toll-like receptor 4 gene MP:0005093 decreased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10549626 737014 Tlr4 toll-like receptor 4 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:15809417 737014 Tlr4 toll-like receptor 4 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:18423196 737014 Tlr4 toll-like receptor 4 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:22796522 737014 Tlr4 toll-like receptor 4 gene MP:0005172 decreased eye pigmentation IEA N RGD:5509061 20111116 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18981228 737014 Tlr4 toll-like receptor 4 gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17519423 737014 Tlr4 toll-like receptor 4 gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:17519423 737014 Tlr4 toll-like receptor 4 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17519423 737014 Tlr4 toll-like receptor 4 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:14699006 737014 Tlr4 toll-like receptor 4 gene MP:0005340 abnormal susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:15249654 737014 Tlr4 toll-like receptor 4 gene MP:0005459 decreased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:15208271 737014 Tlr4 toll-like receptor 4 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:15684036 737014 Tlr4 toll-like receptor 4 gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:15809417 737014 Tlr4 toll-like receptor 4 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:18802464 737014 Tlr4 toll-like receptor 4 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20708624 737014 Tlr4 toll-like receptor 4 gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:15208271 737014 Tlr4 toll-like receptor 4 gene MP:0005667 abnormal circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:17519423 737014 Tlr4 toll-like receptor 4 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16244651 737014 Tlr4 toll-like receptor 4 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:17188246 737014 Tlr4 toll-like receptor 4 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:17693552 737014 Tlr4 toll-like receptor 4 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:17188246 737014 Tlr4 toll-like receptor 4 gene MP:0006071 abnormal retina progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18981228 737014 Tlr4 toll-like receptor 4 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:18981228 737014 Tlr4 toll-like receptor 4 gene MP:0006080 brain ischemia IAGP N RGD:5509061 20141003 MGI PMID:19401158 737014 Tlr4 toll-like receptor 4 gene MP:0008251 abnormal phagocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17767165 737014 Tlr4 toll-like receptor 4 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:18209032 737014 Tlr4 toll-like receptor 4 gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20200618 MGI PMID:15826931 737014 Tlr4 toll-like receptor 4 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:17118979 737014 Tlr4 toll-like receptor 4 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:10549626 737014 Tlr4 toll-like receptor 4 gene MP:0008561 decreased tumor necrosis factor secretion IAGP N RGD:5509061 20141003 MGI PMID:16148141 737014 Tlr4 toll-like receptor 4 gene MP:0008565 decreased interferon-beta secretion IEA N RGD:5509061 20150205 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11489994 737014 Tlr4 toll-like receptor 4 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:12727921 737014 Tlr4 toll-like receptor 4 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:15039466 737014 Tlr4 toll-like receptor 4 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:8982246 737014 Tlr4 toll-like receptor 4 gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:18423196 737014 Tlr4 toll-like receptor 4 gene MP:0008658 decreased interleukin-1 beta secretion IEA N RGD:5509061 20111116 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:17525287 737014 Tlr4 toll-like receptor 4 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:15039466 737014 Tlr4 toll-like receptor 4 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:10549626 737014 Tlr4 toll-like receptor 4 gene MP:0008706 decreased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:17525287 737014 Tlr4 toll-like receptor 4 gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:15731076 737014 Tlr4 toll-like receptor 4 gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:15826931 737014 Tlr4 toll-like receptor 4 gene MP:0008722 abnormal chemokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16244651 737014 Tlr4 toll-like receptor 4 gene MP:0008729 decreased memory B cell number IEA N RGD:5509061 20151015 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:10549626 737014 Tlr4 toll-like receptor 4 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:12727921 737014 Tlr4 toll-like receptor 4 gene MP:0008734 decreased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:19786028 737014 Tlr4 toll-like receptor 4 gene MP:0008751 abnormal interleukin level IAGP N RGD:5509061 20141003 MGI PMID:15731076 737014 Tlr4 toll-like receptor 4 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15731076 737014 Tlr4 toll-like receptor 4 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:15996225 737014 Tlr4 toll-like receptor 4 gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:17707128 737014 Tlr4 toll-like receptor 4 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16244651 737014 Tlr4 toll-like receptor 4 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:19786028 737014 Tlr4 toll-like receptor 4 gene MP:0008891 decreased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16118350 737014 Tlr4 toll-like receptor 4 gene MP:0009269 decreased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:17519423 737014 Tlr4 toll-like receptor 4 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17519423 737014 Tlr4 toll-like receptor 4 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17519423 737014 Tlr4 toll-like receptor 4 gene MP:0009476 enlarged cecum IEA N RGD:5509061 20181227 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0009640 abnormal renal tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18974879 737014 Tlr4 toll-like receptor 4 gene MP:0009764 decreased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17353199 737014 Tlr4 toll-like receptor 4 gene MP:0009878 decreased susceptibility to bone fracture IAGP N RGD:5509061 20141003 MGI PMID:15208271 737014 Tlr4 toll-like receptor 4 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:17704767 737014 Tlr4 toll-like receptor 4 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:15208271 737014 Tlr4 toll-like receptor 4 gene MP:0010159 abnormal enterocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:22796522 737014 Tlr4 toll-like receptor 4 gene MP:0010170 abnormal glial cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:15879150 737014 Tlr4 toll-like receptor 4 gene MP:0010181 decreased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:18802464 737014 Tlr4 toll-like receptor 4 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:17519423 737014 Tlr4 toll-like receptor 4 gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17403033 737014 Tlr4 toll-like receptor 4 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:15039466 737014 Tlr4 toll-like receptor 4 gene MP:0010895 increased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:17053835 737014 Tlr4 toll-like receptor 4 gene MP:0010908 dilated pulmonary alveolar duct IAGP N RGD:5509061 20141003 MGI PMID:17053835 737014 Tlr4 toll-like receptor 4 gene MP:0011079 decreased macrophage cytokine production IEA N RGD:5509061 20151015 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0011081 decreased macrophage apoptosis IEA N RGD:5509061 20151015 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0011277 decreased tail pigmentation IEA N RGD:5509061 20111116 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0011350 abnormal proximal convoluted tubule brush border morphology IAGP N RGD:5509061 20141003 MGI PMID:18974879 737014 Tlr4 toll-like receptor 4 gene MP:0011402 renal cast IAGP N RGD:5509061 20141003 MGI PMID:18974879 737014 Tlr4 toll-like receptor 4 gene MP:0011702 abnormal fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:19786028 737014 Tlr4 toll-like receptor 4 gene MP:0012556 increased cell death IEA N RGD:5509061 20160915 MGI 737014 Tlr4 toll-like receptor 4 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20160324 MGI PMID:25172014 737014 Tlr4 toll-like receptor 4 gene MP:0020947 decreased susceptibility to Orthomyxoviridae infection IAGP N RGD:5509061 20200430 MGI PMID:18423196 737014 Tlr4 toll-like receptor 4 gene MP:0031034 increased susceptibility to Poxviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:18802464 737014 Tlr4 toll-like receptor 4 gene MP:0031617 abnormal skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:17519423 737015 Ptprm protein tyrosine phosphatase receptor type M gene MP:0000188 abnormal circulating glucose level IEA N RGD:5509061 20220519 MGI 737015 Ptprm protein tyrosine phosphatase receptor type M gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 737015 Ptprm protein tyrosine phosphatase receptor type M gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 737015 Ptprm protein tyrosine phosphatase receptor type M gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:15706045 737015 Ptprm protein tyrosine phosphatase receptor type M gene MP:0010090 increased circulating creatine kinase level IEA N RGD:5509061 20211021 MGI 737019 Reg1 regenerating islet-derived 1 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:12475793 737022 Mvp major vault protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12499273 737022 Mvp major vault protein gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12941141 737025 Folh1 folate hydrolase 1 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16809768 737025 Folh1 folate hydrolase 1 gene MP:0000811 hippocampal neuron degeneration IAGP N RGD:5509061 20160811 MGI PMID:25872793 737025 Folh1 folate hydrolase 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:16190866 737025 Folh1 folate hydrolase 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20240627 MGI 737025 Folh1 folate hydrolase 1 gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:16190866 737025 Folh1 folate hydrolase 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:16190866 737025 Folh1 folate hydrolase 1 gene MP:0003858 enhanced coordination IAGP N RGD:5509061 20160811 MGI PMID:25872793 737025 Folh1 folate hydrolase 1 gene MP:0004220 abnormal peripheral nervous system regeneration IAGP N RGD:5509061 20141003 MGI PMID:16190866 737025 Folh1 folate hydrolase 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20160811 MGI PMID:25872793 737025 Folh1 folate hydrolase 1 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20240718 MGI PMID:37349952 737025 Folh1 folate hydrolase 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16809768 737025 Folh1 folate hydrolase 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16809768 737025 Folh1 folate hydrolase 1 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:16190866 737025 Folh1 folate hydrolase 1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:16190866 737025 Folh1 folate hydrolase 1 gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:16190866 737025 Folh1 folate hydrolase 1 gene MP:0012066 decreased astrocyte number IAGP N RGD:5509061 20160811 MGI PMID:25872793 737025 Folh1 folate hydrolase 1 gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20160811 MGI PMID:25872793 737025 Folh1 folate hydrolase 1 gene MP:0012306 enhanced spatial learning IAGP N RGD:5509061 20240718 MGI PMID:37349952 737025 Folh1 folate hydrolase 1 gene MP:0030737 decreased glutamic acid level IAGP N RGD:5509061 20240718 MGI PMID:37349952 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0000640 adrenal gland hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9655498 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:9655498 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:11756502 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22231481 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21885734 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:10448190 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:12973355 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:21885734 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:9620773 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:9655498 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21885734 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21885734 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:12973355 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001748 increased circulating adrenocorticotropin level IAGP N RGD:5509061 20141003 MGI PMID:12973355 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9655498 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001958 emphysema IAGP N RGD:5509061 20141003 MGI PMID:9655498 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0001987 alcohol preference IAGP N RGD:5509061 20141003 MGI PMID:11988580 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0002063 abnormal learning/memory/conditioning IAGP N RGD:5509061 20141003 MGI PMID:10448190 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9620773 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9655498 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0002090 abnormal vision IAGP N RGD:5509061 20141003 MGI PMID:22886732 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12973355 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:21885734 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0002665 decreased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:22886732 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:11756502 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:9620773 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0003953 abnormal hormone level IAGP N RGD:5509061 20141003 MGI PMID:9655498 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0003963 abnormal corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:21885734 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:10919255 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:22886732 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0008289 abnormal adrenal medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:9620773 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0009776 decreased behavioral withdrawal response IAGP N RGD:5509061 20141003 MGI PMID:9620773 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0010149 abnormal synaptic dopamine release IAGP N RGD:5509061 20141003 MGI PMID:21885734 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0010909 pulmonary alveolar hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9655498 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0013366 adrenal gland atrophy IAGP N RGD:5509061 20230907 MGI PMID:11756502 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0014287 decreased adrenal gland zona fasciculata size IAGP N RGD:5509061 20230907 MGI PMID:11756502 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0014287 decreased adrenal gland zona fasciculata size IAGP N RGD:5509061 20230907 MGI PMID:9655498 737026 Crhr1 corticotropin releasing hormone receptor 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:12973355 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0002403 abnormal pre-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0003335 exocrine pancreatic insufficiency IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0005432 abnormal pro-B cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0008208 decreased pro-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0008215 decreased immature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16184191 737029 Serpini2 serine (or cysteine) peptidase inhibitor, clade I, member 2 gene MP:0009160 abnormal pancreatic acinar cell zymogen granule morphology IAGP N RGD:5509061 20141003 MGI PMID:16184191 737030 Sell selectin, lymphocyte gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10500197 737030 Sell selectin, lymphocyte gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11468173 737030 Sell selectin, lymphocyte gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10500197 737030 Sell selectin, lymphocyte gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11050049 737030 Sell selectin, lymphocyte gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11468173 737030 Sell selectin, lymphocyte gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9636189 737030 Sell selectin, lymphocyte gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10500197 737030 Sell selectin, lymphocyte gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11468173 737030 Sell selectin, lymphocyte gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:14614858 737030 Sell selectin, lymphocyte gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9636189 737030 Sell selectin, lymphocyte gene MP:0000223 decreased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:10500197 737030 Sell selectin, lymphocyte gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11468173 737030 Sell selectin, lymphocyte gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:11050049 737030 Sell selectin, lymphocyte gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 737030 Sell selectin, lymphocyte gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7534203 737030 Sell selectin, lymphocyte gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:8976188 737030 Sell selectin, lymphocyte gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:14614858 737030 Sell selectin, lymphocyte gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17182566 737030 Sell selectin, lymphocyte gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:11468173 737030 Sell selectin, lymphocyte gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 737030 Sell selectin, lymphocyte gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:9636189 737030 Sell selectin, lymphocyte gene MP:0001273 decreased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:16452210 737030 Sell selectin, lymphocyte gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:11050049 737030 Sell selectin, lymphocyte gene MP:0001792 impaired wound healing IAGP N RGD:5509061 20141003 MGI PMID:17595378 737030 Sell selectin, lymphocyte gene MP:0001830 decreased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:8627170 737030 Sell selectin, lymphocyte gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:17595378 737030 Sell selectin, lymphocyte gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20200423 MGI PMID:28497779 737030 Sell selectin, lymphocyte gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:11468173 737030 Sell selectin, lymphocyte gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:14662758 737030 Sell selectin, lymphocyte gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16452210 737030 Sell selectin, lymphocyte gene MP:0002148 abnormal hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:8976188 737030 Sell selectin, lymphocyte gene MP:0002148 abnormal hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:9432977 737030 Sell selectin, lymphocyte gene MP:0002351 abnormal cervical lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 737030 Sell selectin, lymphocyte gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8976188 737030 Sell selectin, lymphocyte gene MP:0002421 abnormal cell-mediated immunity IAGP N RGD:5509061 20141003 MGI PMID:8976188 737030 Sell selectin, lymphocyte gene MP:0002423 abnormal mast cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17595378 737030 Sell selectin, lymphocyte gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17595378 737030 Sell selectin, lymphocyte gene MP:0002462 abnormal granulocyte physiology IAGP N RGD:5509061 20200423 MGI PMID:28497779 737030 Sell selectin, lymphocyte gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:14614858 737030 Sell selectin, lymphocyte gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20200423 MGI PMID:28497779 737030 Sell selectin, lymphocyte gene MP:0002534 abnormal type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:8627170 737030 Sell selectin, lymphocyte gene MP:0002908 delayed wound healing IAGP N RGD:5509061 20141003 MGI PMID:17595378 737030 Sell selectin, lymphocyte gene MP:0002942 decreased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:11050049 737030 Sell selectin, lymphocyte gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:11120848 737030 Sell selectin, lymphocyte gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:14614858 737030 Sell selectin, lymphocyte gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:7534203 737030 Sell selectin, lymphocyte gene MP:0003156 abnormal leukocyte migration IAGP N RGD:5509061 20141003 MGI PMID:8976188 737030 Sell selectin, lymphocyte gene MP:0003627 abnormal leukocyte tethering or rolling IAGP N RGD:5509061 20141003 MGI PMID:9636189 737030 Sell selectin, lymphocyte gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:16098130 737030 Sell selectin, lymphocyte gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20141003 MGI PMID:9432977 737030 Sell selectin, lymphocyte gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:16412045 737030 Sell selectin, lymphocyte gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17595378 737030 Sell selectin, lymphocyte gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 737030 Sell selectin, lymphocyte gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:14662758 737030 Sell selectin, lymphocyte gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17182566 737030 Sell selectin, lymphocyte gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210128 MGI 737030 Sell selectin, lymphocyte gene MP:0004972 abnormal regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:17182566 737030 Sell selectin, lymphocyte gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:10500197 737030 Sell selectin, lymphocyte gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:11468173 737030 Sell selectin, lymphocyte gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9636189 737030 Sell selectin, lymphocyte gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9636189 737030 Sell selectin, lymphocyte gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:8976188 737030 Sell selectin, lymphocyte gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:9432977 737030 Sell selectin, lymphocyte gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:14662758 737030 Sell selectin, lymphocyte gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:14614858 737030 Sell selectin, lymphocyte gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16098130 737030 Sell selectin, lymphocyte gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17595378 737030 Sell selectin, lymphocyte gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:16098130 737030 Sell selectin, lymphocyte gene MP:0008083 decreased single-positive T cell number IEA N RGD:5509061 20150305 MGI 737030 Sell selectin, lymphocyte gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:14614858 737030 Sell selectin, lymphocyte gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17182566 737030 Sell selectin, lymphocyte gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8976188 737030 Sell selectin, lymphocyte gene MP:0008470 abnormal spleen B cell follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11468173 737030 Sell selectin, lymphocyte gene MP:0008475 intermingled spleen red and white pulp IAGP N RGD:5509061 20141003 MGI PMID:11468173 737030 Sell selectin, lymphocyte gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:10500197 737030 Sell selectin, lymphocyte gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:16098130 737030 Sell selectin, lymphocyte gene MP:0008723 impaired eosinophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:10500197 737030 Sell selectin, lymphocyte gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:8976188 737030 Sell selectin, lymphocyte gene MP:0009636 small popliteal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8976188 737030 Sell selectin, lymphocyte gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:11120848 737030 Sell selectin, lymphocyte gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:11468173 737030 Sell selectin, lymphocyte gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:7534203 737030 Sell selectin, lymphocyte gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20141003 MGI PMID:9636189 737030 Sell selectin, lymphocyte gene MP:0012194 decreased keratinocyte migration IAGP N RGD:5509061 20141204 MGI PMID:17595378 737030 Sell selectin, lymphocyte gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20240104 MGI PMID:11050049 737030 Sell selectin, lymphocyte gene MP:0014351 abnormal spleen B cell follicle shape IAGP N RGD:5509061 20240104 MGI PMID:11050049 737030 Sell selectin, lymphocyte gene MP:0020001 decreased response to antigen IEA N RGD:5509061 20160616 MGI 737030 Sell selectin, lymphocyte gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:10500197 737030 Sell selectin, lymphocyte gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:11468173 737030 Sell selectin, lymphocyte gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:14614858 737030 Sell selectin, lymphocyte gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:16098130 737030 Sell selectin, lymphocyte gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:7534203 737030 Sell selectin, lymphocyte gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:8976188 737030 Sell selectin, lymphocyte gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:9432977 737030 Sell selectin, lymphocyte gene MP:0020332 impaired leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:9636189 737030 Sell selectin, lymphocyte gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200917 MGI PMID:28497779 737033 Gabrp gamma-aminobutyric acid type A receptor subunit pi gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0000488 abnormal intestinal epithelium morphology IAGP N RGD:5509061 20210729 MGI PMID:31369292 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0000489 abnormal large intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0000491 crypts of Lieberkuhn abscesses IAGP N RGD:5509061 20210729 MGI PMID:31369292 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0000512 intestinal ulcer IAGP N RGD:5509061 20210729 MGI PMID:31369292 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0001263 weight loss IAGP N RGD:5509061 20210729 MGI PMID:31369292 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0001671 abnormal vitamin absorption IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0002083 premature death IAGP N RGD:5509061 20210729 MGI PMID:31369292 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20210729 MGI PMID:31369292 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0004509 abnormal pelvic girdle bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology IAGP N RGD:5509061 20210729 MGI PMID:31369292 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0005036 diarrhea IAGP N RGD:5509061 20210729 MGI PMID:31369292 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0005400 abnormal vitamin level IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0009480 distended cecum IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0009481 cecum inflammation IAGP N RGD:5509061 20210729 MGI PMID:31369292 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0009485 distended ileum IAGP N RGD:5509061 20141003 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0013956 decreased colon length IAGP N RGD:5509061 20210729 MGI PMID:31369292 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0014201 abnormal intestinal epithelium physiology IAGP N RGD:5509061 20210729 MGI PMID:31369292 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0021184 decreased bone mineral density of humerus IAGP N RGD:5509061 20220915 MGI PMID:23104561 737040 Slc5a6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 gene MP:0031154 intestinal hemorrhage IAGP N RGD:5509061 20210729 MGI PMID:31369292 737042 Fgl1 fibrinogen-like protein 1 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0001194 dermatitis IAGP N RGD:5509061 20190221 MGI PMID:30580966 737042 Fgl1 fibrinogen-like protein 1 gene MP:0001257 increased body length IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0002896 abnormal bone mineralization IEA N RGD:5509061 20160804 MGI 737042 Fgl1 fibrinogen-like protein 1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20190221 MGI PMID:30580966 737042 Fgl1 fibrinogen-like protein 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160804 MGI 737042 Fgl1 fibrinogen-like protein 1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20190221 MGI PMID:30580966 737042 Fgl1 fibrinogen-like protein 1 gene MP:0004847 abnormal liver weight IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20190221 MGI PMID:30580966 737042 Fgl1 fibrinogen-like protein 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0009116 abnormal brown fat cell morphology IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0009124 increased brown fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0009355 increased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:23483972 737042 Fgl1 fibrinogen-like protein 1 gene MP:0010847 increased central memory CD8 positive, alpha-beta T cell number IAGP N RGD:5509061 20190221 MGI PMID:30580966 737042 Fgl1 fibrinogen-like protein 1 gene MP:0031115 macrovesicular hepatic steatosis IAGP N RGD:5509061 20200917 MGI PMID:23483972 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0000285 abnormal heart valve morphology IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:11877382 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:9364058 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0000966 decreased sensory neuron number IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0000968 abnormal sensory neuron innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:8145824 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0001024 small L5 dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0001081 abnormal cranial ganglia morphology IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0001085 small petrosal ganglion IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0001088 small nodose ganglion IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0001093 small trigeminal ganglion IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20180726 MGI PMID:29242588 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:8145824 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0001297 microphthalmia IAGP N RGD:5509061 20180726 MGI PMID:29242588 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:8145824 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:8145824 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:8145824 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0001527 athetotic walking movements IAGP N RGD:5509061 20141003 MGI PMID:8145824 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20180726 MGI PMID:29242588 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:8145824 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8145824 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0002092 abnormal eye morphology IAGP N RGD:5509061 20180726 MGI PMID:29242588 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15820690 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0002726 abnormal pulmonary vein morphology IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0002747 abnormal aortic valve morphology IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0003308 abnormal cochlear sensory epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:7588071 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0003986 small cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:7588071 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0003986 small cochlear ganglion IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:7588071 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0003987 small vestibular ganglion IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0004297 abnormal proprioceptive neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0004716 abnormal cochlear nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:11877382 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0004746 abnormal cochlear IHC afferent innervation pattern IAGP N RGD:5509061 20141003 MGI PMID:7588071 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0006404 abnormal lumbar dorsal root ganglion morphology IAGP N RGD:5509061 20170914 MGI PMID:8145824 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:20574020 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0008467 absent proprioceptive neurons IAGP N RGD:5509061 20141003 MGI PMID:15247919 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0008515 thin retina outer nuclear layer IAGP N RGD:5509061 20180726 MGI PMID:29242588 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0010405 ostium secundum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9364058 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160218 MGI PMID:26687362 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0031529 pulmonary valve hyperplasia IAGP N RGD:5509061 20240125 MGI PMID:9405689 737043 Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 gene MP:0031563 pulmonary valve hypertrophy IAGP N RGD:5509061 20240125 MGI PMID:9405689 737048 H1f6 H1.6 linker histone, cluster member gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:15685642 737048 H1f6 H1.6 linker histone, cluster member gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15685642 737048 H1f6 H1.6 linker histone, cluster member gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15685642 737048 H1f6 H1.6 linker histone, cluster member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10688658 737048 H1f6 H1.6 linker histone, cluster member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10933220 737048 H1f6 H1.6 linker histone, cluster member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12930723 737048 H1f6 H1.6 linker histone, cluster member gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19884347 737048 H1f6 H1.6 linker histone, cluster member gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15685642 737048 H1f6 H1.6 linker histone, cluster member gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:15685642 737048 H1f6 H1.6 linker histone, cluster member gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:15685642 737048 H1f6 H1.6 linker histone, cluster member gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:15685642 737048 H1f6 H1.6 linker histone, cluster member gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20200227 MGI PMID:15685642 737054 Amotl2 angiomotin-like 2 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20180329 MGI PMID:24806444 737054 Amotl2 angiomotin-like 2 gene MP:0001258 decreased body length IEA N RGD:5509061 20240523 MGI 737054 Amotl2 angiomotin-like 2 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20240523 MGI 737054 Amotl2 angiomotin-like 2 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20180329 MGI PMID:24806444 737054 Amotl2 angiomotin-like 2 gene MP:0010463 aorta stenosis IAGP N RGD:5509061 20180329 MGI PMID:24806444 737057 Camk1g calcium/calmodulin-dependent protein kinase I gamma gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:17553424 737057 Camk1g calcium/calmodulin-dependent protein kinase I gamma gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19864584 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0001147 small testis IAGP N RGD:5509061 20220203 MGI PMID:20053680 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220203 MGI PMID:20053680 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:23873941 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:23873941 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23873941 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20150910 MGI PMID:23706742 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0001263 weight loss IAGP N RGD:5509061 20150910 MGI PMID:23706742 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:18780892 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:18780892 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220203 MGI PMID:20053680 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220203 MGI PMID:20053680 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15713620 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220203 MGI PMID:20053680 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18780892 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0002685 abnormal spermatogonia proliferation IAGP N RGD:5509061 20220203 MGI PMID:20053680 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220203 MGI PMID:20053680 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19597047 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:18780892 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0003447 decreased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:18780892 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0004647 decreased lumbar vertebrae number IEA N RGD:5509061 20160804 MGI 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220203 MGI PMID:20053680 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220203 MGI PMID:20053680 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005159 azoospermia IAGP N RGD:5509061 20220203 MGI PMID:20053680 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18780892 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15713620 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18594509 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:18594509 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:18780892 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005333 decreased heart rate IEA N RGD:5509061 20111116 MGI 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:19515725 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18780892 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20160804 MGI 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:18780892 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005561 increased mean corpuscular hemoglobin IEA N RGD:5509061 20160804 MGI 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20160804 MGI 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18594509 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005630 increased lung weight IAGP N RGD:5509061 20150910 MGI PMID:23706742 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:18594509 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0006050 pulmonary fibrosis IAGP N RGD:5509061 20150910 MGI PMID:23706742 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0006378 abnormal spermatogonia morphology IAGP N RGD:5509061 20220203 MGI PMID:20053680 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20150910 MGI PMID:23706742 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0009469 increased skin hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:23873941 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:19515725 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:20065293 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:18780892 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20150910 MGI PMID:23706742 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18780892 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:18780892 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11919689 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18544649 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0011102 embryonic lethality, incomplete penetrance IAGP N RGD:5509061 20150910 MGI PMID:23706742 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0011104 embryonic lethality before implantation, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11919689 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18780892 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18780892 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0011416 abnormal testis interstitial tissue morphology IAGP N RGD:5509061 20220203 MGI PMID:20053680 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:18594509 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0011704 decreased fibroblast proliferation IAGP N RGD:5509061 20141003 MGI PMID:18780892 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0013601 increased testis apoptosis IAGP N RGD:5509061 20220203 MGI PMID:20053680 737058 Pik3cb phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta gene MP:0030973 impaired gluconeogenesis IAGP N RGD:5509061 20191226 MGI PMID:18780892 737061 Msln mesothelin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10733593 737063 Prkca protein kinase C, alpha gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16103087 737063 Prkca protein kinase C, alpha gene MP:0002051 increased skin papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:16103087 737063 Prkca protein kinase C, alpha gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:14966518 737063 Prkca protein kinase C, alpha gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17921332 737063 Prkca protein kinase C, alpha gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:14966518 737063 Prkca protein kinase C, alpha gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17921332 737063 Prkca protein kinase C, alpha gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:11923480 737063 Prkca protein kinase C, alpha gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:11923480 737063 Prkca protein kinase C, alpha gene MP:0031619 increased skeletal muscle cell glucose uptake IAGP N RGD:5509061 20240801 MGI PMID:11923480 737065 Mgll monoglyceride lipase gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21454566 737065 Mgll monoglyceride lipase gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 737065 Mgll monoglyceride lipase gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:21454566 737065 Mgll monoglyceride lipase gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:20729846 737065 Mgll monoglyceride lipase gene MP:0001982 decreased chemically-elicited antinociception IAGP N RGD:5509061 20141003 MGI PMID:20729846 737065 Mgll monoglyceride lipase gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21454566 737065 Mgll monoglyceride lipase gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21454566 737065 Mgll monoglyceride lipase gene MP:0002599 increased mean platelet volume IEA N RGD:5509061 20230601 MGI 737065 Mgll monoglyceride lipase gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21454566 737065 Mgll monoglyceride lipase gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21454566 737065 Mgll monoglyceride lipase gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:21454566 737065 Mgll monoglyceride lipase gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20141003 MGI PMID:20729846 737065 Mgll monoglyceride lipase gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:21454566 737065 Mgll monoglyceride lipase gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:21454566 737065 Mgll monoglyceride lipase gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:20729846 737065 Mgll monoglyceride lipase gene MP:0005289 increased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:21454566 737065 Mgll monoglyceride lipase gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:21454566 737065 Mgll monoglyceride lipase gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:20729846 737065 Mgll monoglyceride lipase gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:20729846 737065 Mgll monoglyceride lipase gene MP:0008032 abnormal lipolysis IAGP N RGD:5509061 20141003 MGI PMID:21454566 737065 Mgll monoglyceride lipase gene MP:0008033 impaired lipolysis IAGP N RGD:5509061 20141003 MGI PMID:21454566 737065 Mgll monoglyceride lipase gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20729846 737065 Mgll monoglyceride lipase gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21454566 737065 Mgll monoglyceride lipase gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21454566 737065 Mgll monoglyceride lipase gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:20729846 737065 Mgll monoglyceride lipase gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20240523 MGI 737066 Rpl31 ribosomal protein L31 gene MP:0000585 kinked tail IEA N RGD:5509061 20160331 MGI 737066 Rpl31 ribosomal protein L31 gene MP:0000592 short tail IEA N RGD:5509061 20160331 MGI 737066 Rpl31 ribosomal protein L31 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20160331 MGI 737066 Rpl31 ribosomal protein L31 gene MP:0001891 hydrocephaly IEA N RGD:5509061 20160331 MGI 737069 Canx calnexin gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 737069 Canx calnexin gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 737069 Canx calnexin gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20230601 MGI 737069 Canx calnexin gene MP:0000691 enlarged spleen IEA N RGD:5509061 20230601 MGI 737069 Canx calnexin gene MP:0000703 abnormal thymus morphology IEA N RGD:5509061 20230601 MGI 737069 Canx calnexin gene MP:0000709 enlarged thymus IEA N RGD:5509061 20230601 MGI 737069 Canx calnexin gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20400506 737069 Canx calnexin gene MP:0000759 abnormal skeletal muscle morphology IEA N RGD:5509061 20230601 MGI 737069 Canx calnexin gene MP:0000780 abnormal corpus callosum morphology IAGP N RGD:5509061 20141003 MGI PMID:20400506 737069 Canx calnexin gene MP:0000921 demyelination IAGP N RGD:5509061 20141003 MGI PMID:20400506 737069 Canx calnexin gene MP:0000955 abnormal spinal cord morphology IAGP N RGD:5509061 20141003 MGI PMID:20400506 737069 Canx calnexin gene MP:0001120 abnormal uterus morphology IEA N RGD:5509061 20230601 MGI 737069 Canx calnexin gene MP:0001147 small testis IAGP N RGD:5509061 20240530 MGI PMID:26388295 737069 Canx calnexin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12370287 737069 Canx calnexin gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20400506 737069 Canx calnexin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12370287 737069 Canx calnexin gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:20400506 737069 Canx calnexin gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:20400506 737069 Canx calnexin gene MP:0001516 abnormal motor coordination/balance IAGP N RGD:5509061 20141003 MGI PMID:20400506 737069 Canx calnexin gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20240530 MGI PMID:26388295 737069 Canx calnexin gene MP:0001935 decreased litter size IAGP N RGD:5509061 20240530 MGI PMID:26388295 737069 Canx calnexin gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12370287 737069 Canx calnexin gene MP:0002083 premature death IAGP N RGD:5509061 20240530 MGI PMID:26388295 737069 Canx calnexin gene MP:0003354 astrocytosis IAGP N RGD:5509061 20141003 MGI PMID:20400506 737069 Canx calnexin gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:12370287 737069 Canx calnexin gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:20400506 737069 Canx calnexin gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20240530 MGI PMID:26388295 737069 Canx calnexin gene MP:0004906 enlarged uterus IEA N RGD:5509061 20230601 MGI 737069 Canx calnexin gene MP:0005356 positive geotaxis IAGP N RGD:5509061 20141003 MGI PMID:12370287 737069 Canx calnexin gene MP:0005357 novel environmental response-related retropulsion IAGP N RGD:5509061 20141003 MGI PMID:12370287 737069 Canx calnexin gene MP:0008128 abnormal brain internal capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:20400506 737069 Canx calnexin gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:20400506 737069 Canx calnexin gene MP:0009976 abnormal cerebellar peduncle morphology IAGP N RGD:5509061 20141003 MGI PMID:20400506 737069 Canx calnexin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12370287 737069 Canx calnexin gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20240530 MGI PMID:26388295 737069 Canx calnexin gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20231207 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20200402 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0000538 abnormal urinary bladder morphology IEA N RGD:5509061 20210128 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210128 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0000599 enlarged liver IEA N RGD:5509061 20210826 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20201022 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20210826 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0001147 small testis IEA N RGD:5509061 20210826 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20230720 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20200402 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20160304 MGI PMID:25121932 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20210826 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210128 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210128 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210826 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20160304 MGI PMID:25121932 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0002188 small heart IEA N RGD:5509061 20210520 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20201022 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0002997 enlarged seminal vesicle IEA N RGD:5509061 20210826 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0003068 enlarged kidney IEA N RGD:5509061 20210826 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0003642 absent seminal vesicle IEA N RGD:5509061 20210826 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20230601 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0010052 increased grip strength IEA N RGD:5509061 20220811 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20160304 MGI PMID:25121932 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20160304 MGI PMID:25121932 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0011874 enlarged urinary bladder IEA N RGD:5509061 20210128 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20220519 MGI 737074 Ubtf upstream binding transcription factor, RNA polymerase I gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220519 MGI 737076 Gucy1b2 guanylate cyclase 1, soluble, beta 2 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20161222 MGI PMID:27916458 737076 Gucy1b2 guanylate cyclase 1, soluble, beta 2 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20210805 MGI PMID:34186026 737076 Gucy1b2 guanylate cyclase 1, soluble, beta 2 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IAGP N RGD:5509061 20161222 MGI PMID:27916458 737076 Gucy1b2 guanylate cyclase 1, soluble, beta 2 gene MP:0003462 abnormal response to novel odor IAGP N RGD:5509061 20210805 MGI PMID:34186026 737076 Gucy1b2 guanylate cyclase 1, soluble, beta 2 gene MP:0011677 abnormal olfactory sensory neuron physiology IAGP N RGD:5509061 20161222 MGI PMID:27916458 737076 Gucy1b2 guanylate cyclase 1, soluble, beta 2 gene MP:0031252 abnormal physiological response to hypoxia IAGP N RGD:5509061 20210805 MGI PMID:27916458 737076 Gucy1b2 guanylate cyclase 1, soluble, beta 2 gene MP:0031252 abnormal physiological response to hypoxia IAGP N RGD:5509061 20210805 MGI PMID:34186026 737079 Ppfia4 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 4 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20230601 MGI 737079 Ppfia4 protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), alpha 4 gene MP:0011962 increased cornea thickness IEA N RGD:5509061 20211021 MGI 737081 Pde4a phosphodiesterase 4A, cAMP specific gene MP:0001983 abnormal olfactory system physiology IAGP N RGD:5509061 20141003 MGI PMID:19305400 737081 Pde4a phosphodiesterase 4A, cAMP specific gene MP:0009562 abnormal odor adaptation IAGP N RGD:5509061 20141003 MGI PMID:19305400 737084 Fgf18 fibroblast growth factor 18 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11937494 737084 Fgf18 fibroblast growth factor 18 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:11937494 737084 Fgf18 fibroblast growth factor 18 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:20023171 737084 Fgf18 fibroblast growth factor 18 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:11937494 737084 Fgf18 fibroblast growth factor 18 gene MP:0000427 abnormal hair cycle IAGP N RGD:5509061 20141003 MGI PMID:22297635 737084 Fgf18 fibroblast growth factor 18 gene MP:0000457 maxilla hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:15336546 737084 Fgf18 fibroblast growth factor 18 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20023171 737084 Fgf18 fibroblast growth factor 18 gene MP:0001510 abnormal coat appearance IAGP N RGD:5509061 20141003 MGI PMID:22297635 737084 Fgf18 fibroblast growth factor 18 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:20023171 737084 Fgf18 fibroblast growth factor 18 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0002187 abnormal fibula morphology IAGP N RGD:5509061 20141003 MGI PMID:11937494 737084 Fgf18 fibroblast growth factor 18 gene MP:0002314 abnormal respiratory mechanics IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:11937494 737084 Fgf18 fibroblast growth factor 18 gene MP:0002835 abnormal cranial suture morphology IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0003072 abnormal metatarsal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0003420 delayed intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0003641 small lung IAGP N RGD:5509061 20141003 MGI PMID:15336546 737084 Fgf18 fibroblast growth factor 18 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:15336546 737084 Fgf18 fibroblast growth factor 18 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:20023171 737084 Fgf18 fibroblast growth factor 18 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:11937494 737084 Fgf18 fibroblast growth factor 18 gene MP:0004358 bowed tibia IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:11937494 737084 Fgf18 fibroblast growth factor 18 gene MP:0004374 bowed radius IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0004734 small thoracic cavity IAGP N RGD:5509061 20141003 MGI PMID:11937494 737084 Fgf18 fibroblast growth factor 18 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:20023171 737084 Fgf18 fibroblast growth factor 18 gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0008395 abnormal osteoblast differentiation IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0008858 abnormal hair cycle anagen phase IAGP N RGD:5509061 20141003 MGI PMID:22297635 737084 Fgf18 fibroblast growth factor 18 gene MP:0008860 abnormal hair cycle telogen phase IAGP N RGD:5509061 20141003 MGI PMID:22297635 737084 Fgf18 fibroblast growth factor 18 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0009886 failure of palatal shelf elevation IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0010743 delayed cranial suture closure IAGP N RGD:5509061 20171102 MGI PMID:11937494 737084 Fgf18 fibroblast growth factor 18 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:15336546 737084 Fgf18 fibroblast growth factor 18 gene MP:0010976 small lung lobe IAGP N RGD:5509061 20141003 MGI PMID:15336546 737084 Fgf18 fibroblast growth factor 18 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20023171 737084 Fgf18 fibroblast growth factor 18 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11937493 737084 Fgf18 fibroblast growth factor 18 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20023171 737084 Fgf18 fibroblast growth factor 18 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11937494 737084 Fgf18 fibroblast growth factor 18 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20141003 MGI PMID:15336546 737084 Fgf18 fibroblast growth factor 18 gene MP:0030315 small neurocranium IAGP N RGD:5509061 20171109 MGI PMID:11937493 737087 Rgs10 regulator of G-protein signalling 10 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:17626792 737087 Rgs10 regulator of G-protein signalling 10 gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17626792 737087 Rgs10 regulator of G-protein signalling 10 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17626792 737087 Rgs10 regulator of G-protein signalling 10 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:17626792 737087 Rgs10 regulator of G-protein signalling 10 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17626792 737087 Rgs10 regulator of G-protein signalling 10 gene MP:0003408 increased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:17626792 737087 Rgs10 regulator of G-protein signalling 10 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17626792 737087 Rgs10 regulator of G-protein signalling 10 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17626792 737087 Rgs10 regulator of G-protein signalling 10 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20111116 MGI 737087 Rgs10 regulator of G-protein signalling 10 gene MP:0005559 increased circulating glucose level IEA N RGD:5509061 20111116 MGI 737087 Rgs10 regulator of G-protein signalling 10 gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17626792 737087 Rgs10 regulator of G-protein signalling 10 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:17626792 737087 Rgs10 regulator of G-protein signalling 10 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17626792 737089 Acsl1 acyl-CoA synthetase long-chain family member 1 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20180111 MGI PMID:20620995 737089 Acsl1 acyl-CoA synthetase long-chain family member 1 gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20180111 MGI PMID:20620995 737089 Acsl1 acyl-CoA synthetase long-chain family member 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20180111 MGI PMID:20620995 737089 Acsl1 acyl-CoA synthetase long-chain family member 1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20180111 MGI PMID:20620995 737089 Acsl1 acyl-CoA synthetase long-chain family member 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:19648649 737089 Acsl1 acyl-CoA synthetase long-chain family member 1 gene MP:0003442 decreased circulating glycerol level IAGP N RGD:5509061 20180111 MGI PMID:20620995 737089 Acsl1 acyl-CoA synthetase long-chain family member 1 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20180111 MGI PMID:20620995 737089 Acsl1 acyl-CoA synthetase long-chain family member 1 gene MP:0005317 increased triglyceride level IAGP N RGD:5509061 20180111 MGI PMID:20620995 737089 Acsl1 acyl-CoA synthetase long-chain family member 1 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20180111 MGI PMID:20620995 737089 Acsl1 acyl-CoA synthetase long-chain family member 1 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20180111 MGI PMID:20620995 737089 Acsl1 acyl-CoA synthetase long-chain family member 1 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20180111 MGI PMID:20620995 737089 Acsl1 acyl-CoA synthetase long-chain family member 1 gene MP:0011579 decreased lipoprotein lipase activity IAGP N RGD:5509061 20180111 MGI PMID:20620995 737089 Acsl1 acyl-CoA synthetase long-chain family member 1 gene MP:0014142 increased body fat mass IAGP N RGD:5509061 20180111 MGI PMID:20620995 737089 Acsl1 acyl-CoA synthetase long-chain family member 1 gene MP:0014172 decreased fatty acid oxidation IAGP N RGD:5509061 20180111 MGI PMID:20620995 737095 Kcnip2 Kv channel-interacting protein 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:11747815 737095 Kcnip2 Kv channel-interacting protein 2 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:11747815 737095 Kcnip2 Kv channel-interacting protein 2 gene MP:0003897 abnormal ST segment IAGP N RGD:5509061 20141003 MGI PMID:11747815 737095 Kcnip2 Kv channel-interacting protein 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20150205 MGI PMID:23713033 737097 Tnfsf15 tumor necrosis factor (ligand) superfamily, member 15 gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:24140642 737097 Tnfsf15 tumor necrosis factor (ligand) superfamily, member 15 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20141003 MGI PMID:24140642 737097 Tnfsf15 tumor necrosis factor (ligand) superfamily, member 15 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:18411337 737097 Tnfsf15 tumor necrosis factor (ligand) superfamily, member 15 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:24140642 737097 Tnfsf15 tumor necrosis factor (ligand) superfamily, member 15 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:24140642 737097 Tnfsf15 tumor necrosis factor (ligand) superfamily, member 15 gene MP:0008044 increased NK cell number IEA N RGD:5509061 20141003 MGI 737097 Tnfsf15 tumor necrosis factor (ligand) superfamily, member 15 gene MP:0008098 decreased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:24140642 737097 Tnfsf15 tumor necrosis factor (ligand) superfamily, member 15 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:24140642 737097 Tnfsf15 tumor necrosis factor (ligand) superfamily, member 15 gene MP:0008115 abnormal dendritic cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:18411337 737097 Tnfsf15 tumor necrosis factor (ligand) superfamily, member 15 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:24140642 737097 Tnfsf15 tumor necrosis factor (ligand) superfamily, member 15 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:24140642 737097 Tnfsf15 tumor necrosis factor (ligand) superfamily, member 15 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:24140642 737097 Tnfsf15 tumor necrosis factor (ligand) superfamily, member 15 gene MP:0010187 decreased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:24140642 737106 Rgs8 regulator of G-protein signaling 8 gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:8917583 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0000746 weakness IAGP N RGD:5509061 20141003 MGI PMID:9362465 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:8917583 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:22178625 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:8917583 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:9362465 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8917583 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9362465 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0001529 abnormal vocalization IAGP N RGD:5509061 20141003 MGI PMID:22178625 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0001950 abnormal respiratory sounds IAGP N RGD:5509061 20141003 MGI PMID:22178625 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8917583 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9362465 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22178625 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:8917583 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:22178625 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0002913 abnormal PNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:8917583 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22178625 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:8917583 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0004243 abnormal motor nerve collateral sprouting IAGP N RGD:5509061 20141003 MGI PMID:9362465 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:22178625 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:8917583 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:9362465 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:8917583 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20141003 MGI PMID:9362465 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:22178625 737109 Chrne cholinergic receptor, nicotinic, epsilon polypeptide gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:8917583 737110 Gas5 growth arrest specific 5 gene MP:0000066 osteoporosis IAGP N RGD:5509061 20210114 MGI PMID:33006314 737110 Gas5 growth arrest specific 5 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20210114 MGI PMID:33006314 737110 Gas5 growth arrest specific 5 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20210114 MGI PMID:33006314 737110 Gas5 growth arrest specific 5 gene MP:0002999 abnormal bone healing IAGP N RGD:5509061 20210114 MGI PMID:33006314 737110 Gas5 growth arrest specific 5 gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20210114 MGI PMID:33006314 737110 Gas5 growth arrest specific 5 gene MP:0010869 decreased bone trabecula number IAGP N RGD:5509061 20210114 MGI PMID:33006314 737110 Gas5 growth arrest specific 5 gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20210114 MGI PMID:33006314 737110 Gas5 growth arrest specific 5 gene MP:0011711 impaired osteoblast differentiation IAGP N RGD:5509061 20210114 MGI PMID:33006314 737110 Gas5 growth arrest specific 5 gene MP:0013630 increased bone trabecular spacing IAGP N RGD:5509061 20210114 MGI PMID:33006314 737112 Wfdc18 WAP four-disulfide core domain 18 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20201022 MGI 737112 Wfdc18 WAP four-disulfide core domain 18 gene MP:0003020 decreased circulating chloride level IEA N RGD:5509061 20210520 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:7097320 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20240523 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0000223 decreased monocyte cell number IEA N RGD:5509061 20231207 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0000416 sparse hair IEA N RGD:5509061 20111116 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0000743 muscle spasm IEA N RGD:5509061 20111116 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0000745 tremors IEA N RGD:5509061 20231207 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0000755 hindlimb paralysis IEA N RGD:5509061 20111116 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0000756 forelimb paralysis IEA N RGD:5509061 20111116 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:3621304 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20231207 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7097320 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20210805 MGI PMID:34142127 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001297 microphthalmia IEA N RGD:5509061 20231207 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001388 abnormal stationary movement IEA N RGD:5509061 20111116 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001393 ataxia IEA N RGD:5509061 20141003 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20231207 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:7097320 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20231207 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20231207 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001513 limb grasping IEA N RGD:5509061 20111116 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:10628777 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:16943554 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:2453798 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001524 impaired limb coordination IAGP N RGD:5509061 20141003 MGI PMID:7097320 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:10628777 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:7097320 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:10628777 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001924 infertility IEA N RGD:5509061 20111116 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10628777 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0001926 female infertility IEA N RGD:5509061 20240523 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0002067 abnormal sensory capabilities/reflexes/nociception IEA N RGD:5509061 20141003 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10628777 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20231207 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:10628777 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:2453798 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:7097320 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20231207 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20231207 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:2453798 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0002862 abnormal righting response IEA N RGD:5509061 20111116 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20240523 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:16717059 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:2453798 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0003491 abnormal voluntary movement IAGP N RGD:5509061 20141003 MGI PMID:7097320 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0004143 muscle hypertonia IEA N RGD:5509061 20141003 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:2453798 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:7097320 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:10628777 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20210805 MGI PMID:34142127 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20231207 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0004818 increased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:7097320 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20231207 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20240523 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20240523 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20240523 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20240523 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0005405 axon degeneration IAGP N RGD:5509061 20141003 MGI PMID:7097320 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20240523 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:16943554 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20231207 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0009046 muscle twitch IAGP N RGD:5509061 20141003 MGI PMID:6589628 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20231207 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0009434 paraparesis IEA N RGD:5509061 20111116 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20231207 MGI 737113 Clcn1 chloride channel, voltage-sensitive 1 gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20231207 MGI 737119 Kitl kit ligand gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15765184 737119 Kitl kit ligand gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:15765184 737119 Kitl kit ligand gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:8875893 737119 Kitl kit ligand gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:22281595 737119 Kitl kit ligand gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:12881302 737119 Kitl kit ligand gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0000324 increased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:7533739 737119 Kitl kit ligand gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22281595 737119 Kitl kit ligand gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:367470 737119 Kitl kit ligand gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:8605335 737119 Kitl kit ligand gene MP:0000336 decreased mast cell number IAGP N RGD:5509061 20141003 MGI PMID:9751763 737119 Kitl kit ligand gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0000370 head blaze IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:10932191 737119 Kitl kit ligand gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:4392283 737119 Kitl kit ligand gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:6630999 737119 Kitl kit ligand gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:7533739 737119 Kitl kit ligand gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:8875893 737119 Kitl kit ligand gene MP:0000371 diluted coat color IAGP N RGD:5509061 20141003 MGI PMID:9360640 737119 Kitl kit ligand gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4392283 737119 Kitl kit ligand gene MP:0000372 irregular coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7683280 737119 Kitl kit ligand gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:12881302 737119 Kitl kit ligand gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0000373 belly spot IAGP N RGD:5509061 20141003 MGI PMID:8875893 737119 Kitl kit ligand gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:5296838 737119 Kitl kit ligand gene MP:0000471 abnormal stomach epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:1325193 737119 Kitl kit ligand gene MP:0000472 abnormal stomach non-glandular epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:1325193 737119 Kitl kit ligand gene MP:0000600 liver hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22281595 737119 Kitl kit ligand gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:12881302 737119 Kitl kit ligand gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22281595 737119 Kitl kit ligand gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:22281595 737119 Kitl kit ligand gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0000913 abnormal brain development IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:1383087 737119 Kitl kit ligand gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:7683280 737119 Kitl kit ligand gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:7533739 737119 Kitl kit ligand gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:7683280 737119 Kitl kit ligand gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:7533739 737119 Kitl kit ligand gene MP:0001144 vagina atresia IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:1383087 737119 Kitl kit ligand gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:1383087 737119 Kitl kit ligand gene MP:0001188 hyperpigmentation IAGP N RGD:5509061 20141003 MGI PMID:7533739 737119 Kitl kit ligand gene MP:0001189 absent skin pigmentation IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:319242 737119 Kitl kit ligand gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15765184 737119 Kitl kit ligand gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:319242 737119 Kitl kit ligand gene MP:0001265 decreased body size IEA N RGD:5509061 20141003 MGI 737119 Kitl kit ligand gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:1325193 737119 Kitl kit ligand gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:1711207 737119 Kitl kit ligand gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22281595 737119 Kitl kit ligand gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:367470 737119 Kitl kit ligand gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:5296838 737119 Kitl kit ligand gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:8849899 737119 Kitl kit ligand gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15765184 737119 Kitl kit ligand gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:1325193 737119 Kitl kit ligand gene MP:0001921 reduced fertility IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:8875893 737119 Kitl kit ligand gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:8875893 737119 Kitl kit ligand gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9360640 737119 Kitl kit ligand gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:1170085 737119 Kitl kit ligand gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:1711207 737119 Kitl kit ligand gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:1383087 737119 Kitl kit ligand gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:7533739 737119 Kitl kit ligand gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:7683280 737119 Kitl kit ligand gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:8875893 737119 Kitl kit ligand gene MP:0001935 decreased litter size IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0002014 increased papilloma incidence IAGP N RGD:5509061 20141003 MGI PMID:1325193 737119 Kitl kit ligand gene MP:0002019 abnormal tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:319242 737119 Kitl kit ligand gene MP:0002020 increased tumor incidence IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:319242 737119 Kitl kit ligand gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:14871802 737119 Kitl kit ligand gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:1711207 737119 Kitl kit ligand gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4392283 737119 Kitl kit ligand gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7533739 737119 Kitl kit ligand gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:8605335 737119 Kitl kit ligand gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:319242 737119 Kitl kit ligand gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:5296838 737119 Kitl kit ligand gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:7533739 737119 Kitl kit ligand gene MP:0002098 abnormal vibrissa morphology IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:15765184 737119 Kitl kit ligand gene MP:0002128 abnormal blood circulation IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0002216 abnormal seminiferous tubule morphology IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:8875893 737119 Kitl kit ligand gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0002594 low mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12647239 737119 Kitl kit ligand gene MP:0002640 reticulocytosis IEA N RGD:5509061 20141003 MGI 737119 Kitl kit ligand gene MP:0002777 absent ovarian follicles IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:4392283 737119 Kitl kit ligand gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:7683280 737119 Kitl kit ligand gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:8875893 737119 Kitl kit ligand gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:8875893 737119 Kitl kit ligand gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12647239 737119 Kitl kit ligand gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22281595 737119 Kitl kit ligand gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8875893 737119 Kitl kit ligand gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:7533739 737119 Kitl kit ligand gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:7683280 737119 Kitl kit ligand gene MP:0002938 white spotting IAGP N RGD:5509061 20141003 MGI PMID:9360640 737119 Kitl kit ligand gene MP:0002939 head spot IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0002939 head spot IAGP N RGD:5509061 20141003 MGI PMID:3342938 737119 Kitl kit ligand gene MP:0002939 head spot IAGP N RGD:5509061 20141003 MGI PMID:4392283 737119 Kitl kit ligand gene MP:0002939 head spot IAGP N RGD:5509061 20141003 MGI PMID:8875893 737119 Kitl kit ligand gene MP:0002940 variable body spotting IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20141003 MGI PMID:15917341 737119 Kitl kit ligand gene MP:0002982 abnormal primordial germ cell migration IAGP N RGD:5509061 20141003 MGI PMID:17107997 737119 Kitl kit ligand gene MP:0003054 spina bifida IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0003282 gastric ulcer IAGP N RGD:5509061 20141003 MGI PMID:1325193 737119 Kitl kit ligand gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20141003 MGI PMID:319242 737119 Kitl kit ligand gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:12881302 737119 Kitl kit ligand gene MP:0003992 increased mortality induced by ionizing radiation IAGP N RGD:5509061 20141003 MGI PMID:9751763 737119 Kitl kit ligand gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:12881302 737119 Kitl kit ligand gene MP:0004478 increased testicular teratoma incidence IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0004806 absent germ cells IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:1383087 737119 Kitl kit ligand gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:7683280 737119 Kitl kit ligand gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:15765184 737119 Kitl kit ligand gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:15765184 737119 Kitl kit ligand gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0005103 abnormal retina pigmentation IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:3342938 737119 Kitl kit ligand gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:4392283 737119 Kitl kit ligand gene MP:0005171 absent coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:6630999 737119 Kitl kit ligand gene MP:0005175 non-pigmented tail tip IAGP N RGD:5509061 20141003 MGI PMID:6630999 737119 Kitl kit ligand gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:8605335 737119 Kitl kit ligand gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:1383087 737119 Kitl kit ligand gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:7533739 737119 Kitl kit ligand gene MP:0005431 decreased oocyte number IAGP N RGD:5509061 20141003 MGI PMID:7683280 737119 Kitl kit ligand gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:8875893 737119 Kitl kit ligand gene MP:0005641 increased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:8875893 737119 Kitl kit ligand gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:367470 737119 Kitl kit ligand gene MP:0006205 embryonic lethality between implantation and somite formation IEA N RGD:5509061 20141003 MGI 737119 Kitl kit ligand gene MP:0006410 abnormal common myeloid progenitor cell morphology IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0008237 abnormal ventral coat pigmentation IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0008390 abnormal primordial germ cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:15917341 737119 Kitl kit ligand gene MP:0008390 abnormal primordial germ cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:17107997 737119 Kitl kit ligand gene MP:0008391 abnormal primordial germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15917341 737119 Kitl kit ligand gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:1170085 737119 Kitl kit ligand gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:1383087 737119 Kitl kit ligand gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:15917341 737119 Kitl kit ligand gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:7533739 737119 Kitl kit ligand gene MP:0008392 decreased primordial germ cell number IAGP N RGD:5509061 20141003 MGI PMID:7683280 737119 Kitl kit ligand gene MP:0008393 absent primordial germ cells IAGP N RGD:5509061 20141003 MGI PMID:12881302 737119 Kitl kit ligand gene MP:0008393 absent primordial germ cells IAGP N RGD:5509061 20141003 MGI PMID:15917341 737119 Kitl kit ligand gene MP:0008762 embryonic lethality IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0008857 myelencephalic blebs IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19874813 737119 Kitl kit ligand gene MP:0009278 abnormal bone marrow cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22281595 737119 Kitl kit ligand gene MP:0009379 abnormal foot pigmentation IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:9751763 737119 Kitl kit ligand gene MP:0009783 abnormal melanoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:1280558 737119 Kitl kit ligand gene MP:0009933 abnormal tail hair pigmentation IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0009934 abnormal hind foot hair pigmentation IEA N RGD:5509061 20141003 MGI 737119 Kitl kit ligand gene MP:0010124 decreased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:15765184 737119 Kitl kit ligand gene MP:0010275 increased melanoma incidence IAGP N RGD:5509061 20141003 MGI PMID:14871802 737119 Kitl kit ligand gene MP:0010383 increased adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:1383087 737119 Kitl kit ligand gene MP:0010784 abnormal forestomach morphology IAGP N RGD:5509061 20141003 MGI PMID:1325193 737119 Kitl kit ligand gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:15765184 737119 Kitl kit ligand gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12647239 737119 Kitl kit ligand gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22281595 737119 Kitl kit ligand gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12647239 737119 Kitl kit ligand gene MP:0011091 prenatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0011092 embryonic lethality, complete penetrance IEA N RGD:5509061 20120126 MGI 737119 Kitl kit ligand gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12881302 737119 Kitl kit ligand gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8849899 737119 Kitl kit ligand gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12242245 737119 Kitl kit ligand gene MP:0011182 decreased hematopoietic cell number IAGP N RGD:5509061 20141003 MGI PMID:22281595 737119 Kitl kit ligand gene MP:0011188 increased erythrocyte protoporphyrin level IAGP N RGD:5509061 20141003 MGI PMID:658175 737119 Kitl kit ligand gene MP:0011277 decreased tail pigmentation IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20170803 MGI PMID:8875893 737119 Kitl kit ligand gene MP:0011278 increased ear pigmentation IAGP N RGD:5509061 20170914 MGI PMID:9360640 737119 Kitl kit ligand gene MP:0011279 decreased ear pigmentation IEA N RGD:5509061 20111116 MGI 737119 Kitl kit ligand gene MP:0011568 decreased foot pigmentation IEA N RGD:5509061 20141003 MGI 737119 Kitl kit ligand gene MP:0030934 decreased primordial germ cell proliferation IAGP N RGD:5509061 20190411 MGI PMID:15917341 737119 Kitl kit ligand gene MP:0030935 increased primordial germ cell apoptosis IAGP N RGD:5509061 20190411 MGI PMID:15917341 737120 Smarcd2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 737120 Smarcd2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20211021 MGI 737120 Smarcd2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2 gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220811 MGI 737120 Smarcd2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 737120 Smarcd2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2 gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20230831 MGI PMID:28303890 737121 Ccn5 cellular communication network factor 5 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20240314 MGI PMID:29396648 737121 Ccn5 cellular communication network factor 5 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 737122 Bcar1 breast cancer anti-estrogen resistance 1 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20141003 MGI PMID:9697697 737122 Bcar1 breast cancer anti-estrogen resistance 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9697697 737122 Bcar1 breast cancer anti-estrogen resistance 1 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:9697697 737122 Bcar1 breast cancer anti-estrogen resistance 1 gene MP:0000358 abnormal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9697697 737122 Bcar1 breast cancer anti-estrogen resistance 1 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:9697697 737122 Bcar1 breast cancer anti-estrogen resistance 1 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:9697697 737122 Bcar1 breast cancer anti-estrogen resistance 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9697697 737122 Bcar1 breast cancer anti-estrogen resistance 1 gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:9697697 737122 Bcar1 breast cancer anti-estrogen resistance 1 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9697697 737122 Bcar1 breast cancer anti-estrogen resistance 1 gene MP:0005590 increased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:9697697 737122 Bcar1 breast cancer anti-estrogen resistance 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9697697 737122 Bcar1 breast cancer anti-estrogen resistance 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9697697 737123 Slc6a18 solute carrier family 6 (neurotransmitter transporter), member 18 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:15121838 737123 Slc6a18 solute carrier family 6 (neurotransmitter transporter), member 18 gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15121838 737123 Slc6a18 solute carrier family 6 (neurotransmitter transporter), member 18 gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20141003 MGI PMID:15121838 737123 Slc6a18 solute carrier family 6 (neurotransmitter transporter), member 18 gene MP:0011417 abnormal renal transport IAGP N RGD:5509061 20141003 MGI PMID:15121838 737123 Slc6a18 solute carrier family 6 (neurotransmitter transporter), member 18 gene MP:0030616 hyperglycinuria IAGP N RGD:5509061 20180906 MGI PMID:15121838 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:14657344 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:21193513 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21193513 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21220308 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17258700 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18538341 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:23318872 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0002741 small olfactory bulb IAGP N RGD:5509061 20141003 MGI PMID:23318872 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:18538341 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:21220308 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:21193513 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0003896 prolonged PR interval IAGP N RGD:5509061 20141003 MGI PMID:21193513 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0003928 increased heart rate variability IAGP N RGD:5509061 20141003 MGI PMID:21193513 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0004115 abnormal sinoatrial node morphology IAGP N RGD:5509061 20141003 MGI PMID:21193513 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:18219271 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:18219271 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:18538341 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:21193513 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:21220308 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0006142 abnormal sinoatrial node conduction IAGP N RGD:5509061 20141003 MGI PMID:21220308 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0009948 abnormal olfactory bulb glomerular layer morphology IAGP N RGD:5509061 20141003 MGI PMID:23318872 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:21193513 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:21220308 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0010520 sinoatrial block IAGP N RGD:5509061 20141003 MGI PMID:18538341 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0011092 embryonic lethality, complete penetrance IEA N RGD:5509061 20141003 MGI 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14657344 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18219271 737127 Hcn4 hyperpolarization-activated, cyclic nucleotide-gated K+ 4 gene MP:0011953 prolonged PQ interval IAGP N RGD:5509061 20141003 MGI PMID:21220308 737131 Rapgef4 Rap guanine nucleotide exchange factor (GEF) 4 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20211021 MGI 737131 Rapgef4 Rap guanine nucleotide exchange factor (GEF) 4 gene MP:0003564 abnormal insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:18040047 737131 Rapgef4 Rap guanine nucleotide exchange factor (GEF) 4 gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:23363625 737131 Rapgef4 Rap guanine nucleotide exchange factor (GEF) 4 gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21041529 737131 Rapgef4 Rap guanine nucleotide exchange factor (GEF) 4 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:23363625 737131 Rapgef4 Rap guanine nucleotide exchange factor (GEF) 4 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20211021 MGI 737131 Rapgef4 Rap guanine nucleotide exchange factor (GEF) 4 gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 737136 Rtn4rl1 reticulon 4 receptor-like 1 gene MP:0000607 abnormal hepatocyte morphology IEA N RGD:5509061 20111116 MGI 737136 Rtn4rl1 reticulon 4 receptor-like 1 gene MP:0002628 hepatic steatosis IEA N RGD:5509061 20111116 MGI 737136 Rtn4rl1 reticulon 4 receptor-like 1 gene MP:0002928 abnormal bile duct morphology IEA N RGD:5509061 20111116 MGI 737136 Rtn4rl1 reticulon 4 receptor-like 1 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:22406547 737136 Rtn4rl1 reticulon 4 receptor-like 1 gene MP:0030013 enhanced central nervous system regeneration IAGP N RGD:5509061 20170713 MGI PMID:22406547 737139 Bok BCL2-related ovarian killer gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20221215 MGI 737139 Bok BCL2-related ovarian killer gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20211021 MGI 737139 Bok BCL2-related ovarian killer gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22281706 737139 Bok BCL2-related ovarian killer gene MP:0004955 increased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:22281706 737139 Bok BCL2-related ovarian killer gene MP:0005011 increased eosinophil cell number IEA N RGD:5509061 20211021 MGI 737139 Bok BCL2-related ovarian killer gene MP:0005278 abnormal cholesterol homeostasis IEA N RGD:5509061 20231207 MGI 737139 Bok BCL2-related ovarian killer gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:22281706 737141 Gata4 GATA binding protein 4 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:17069789 737141 Gata4 GATA binding protein 4 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15464586 737141 Gata4 GATA binding protein 4 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9136932 737141 Gata4 GATA binding protein 4 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:9136933 737141 Gata4 GATA binding protein 4 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9136933 737141 Gata4 GATA binding protein 4 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16514068 737141 Gata4 GATA binding protein 4 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:16514068 737141 Gata4 GATA binding protein 4 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:24380800 737141 Gata4 GATA binding protein 4 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20240118 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:15464586 737141 Gata4 GATA binding protein 4 gene MP:0000281 abnormal interventricular septum morphology IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15464586 737141 Gata4 GATA binding protein 4 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15902305 737141 Gata4 GATA binding protein 4 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:19411759 737141 Gata4 GATA binding protein 4 gene MP:0000297 abnormal atrioventricular cushion morphology IAGP N RGD:5509061 20141003 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0000474 abnormal foregut morphology IAGP N RGD:5509061 20141003 MGI PMID:9136932 737141 Gata4 GATA binding protein 4 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:24380800 737141 Gata4 GATA binding protein 4 gene MP:0000601 small liver IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0001127 small ovary IAGP N RGD:5509061 20220602 MGI PMID:21248289 737141 Gata4 GATA binding protein 4 gene MP:0001147 small testis IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:17069789 737141 Gata4 GATA binding protein 4 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:17142311 737141 Gata4 GATA binding protein 4 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:19411759 737141 Gata4 GATA binding protein 4 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16514068 737141 Gata4 GATA binding protein 4 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21746915 737141 Gata4 GATA binding protein 4 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20141003 MGI PMID:9136933 737141 Gata4 GATA binding protein 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9136932 737141 Gata4 GATA binding protein 4 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:9136933 737141 Gata4 GATA binding protein 4 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:15464586 737141 Gata4 GATA binding protein 4 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9136932 737141 Gata4 GATA binding protein 4 gene MP:0001704 abnormal dorsal-ventral axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9136933 737141 Gata4 GATA binding protein 4 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:9136932 737141 Gata4 GATA binding protein 4 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:9136933 737141 Gata4 GATA binding protein 4 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0001786 skin edema IAGP N RGD:5509061 20141003 MGI PMID:19411759 737141 Gata4 GATA binding protein 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19411759 737141 Gata4 GATA binding protein 4 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220602 MGI PMID:21248289 737141 Gata4 GATA binding protein 4 gene MP:0001926 female infertility IAGP N RGD:5509061 20220602 MGI PMID:21248289 737141 Gata4 GATA binding protein 4 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220602 MGI PMID:21248289 737141 Gata4 GATA binding protein 4 gene MP:0001938 delayed sexual maturation IAGP N RGD:5509061 20220602 MGI PMID:21248289 737141 Gata4 GATA binding protein 4 gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20160623 MGI PMID:25807280 737141 Gata4 GATA binding protein 4 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20220602 MGI PMID:21248289 737141 Gata4 GATA binding protein 4 gene MP:0002058 neonatal lethality IAGP N RGD:5509061 20160623 MGI PMID:25807280 737141 Gata4 GATA binding protein 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16514068 737141 Gata4 GATA binding protein 4 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:9136933 737141 Gata4 GATA binding protein 4 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:9136933 737141 Gata4 GATA binding protein 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:15464586 737141 Gata4 GATA binding protein 4 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:12223418 737141 Gata4 GATA binding protein 4 gene MP:0002213 true hermaphroditism IAGP N RGD:5509061 20201224 MGI PMID:17848526 737141 Gata4 GATA binding protein 4 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0002652 thin myocardium IAGP N RGD:5509061 20141003 MGI PMID:24380800 737141 Gata4 GATA binding protein 4 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15902305 737141 Gata4 GATA binding protein 4 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:16514068 737141 Gata4 GATA binding protein 4 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20220609 MGI PMID:30793514 737141 Gata4 GATA binding protein 4 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12223418 737141 Gata4 GATA binding protein 4 gene MP:0002784 abnormal Sertoli cell morphology IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0002925 abnormal cardiovascular development IAGP N RGD:5509061 20141003 MGI PMID:24380800 737141 Gata4 GATA binding protein 4 gene MP:0002950 abnormal neural crest cell migration IAGP N RGD:5509061 20230216 MGI PMID:29311329 737141 Gata4 GATA binding protein 4 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:12223418 737141 Gata4 GATA binding protein 4 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20201224 MGI PMID:17848526 737141 Gata4 GATA binding protein 4 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0003205 testicular atrophy IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16514068 737141 Gata4 GATA binding protein 4 gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20220602 MGI PMID:21248289 737141 Gata4 GATA binding protein 4 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15902305 737141 Gata4 GATA binding protein 4 gene MP:0003567 abnormal fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:16514068 737141 Gata4 GATA binding protein 4 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:17069789 737141 Gata4 GATA binding protein 4 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20141003 MGI PMID:22723016 737141 Gata4 GATA binding protein 4 gene MP:0003924 diaphragmatic hernia IAGP N RGD:5509061 20160623 MGI PMID:25807280 737141 Gata4 GATA binding protein 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15902305 737141 Gata4 GATA binding protein 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9136933 737141 Gata4 GATA binding protein 4 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17069789 737141 Gata4 GATA binding protein 4 gene MP:0004056 abnormal myocardium compact layer morphology IAGP N RGD:5509061 20141003 MGI PMID:15464586 737141 Gata4 GATA binding protein 4 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:19411759 737141 Gata4 GATA binding protein 4 gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20240118 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0004062 dilated heart right atrium IAGP N RGD:5509061 20231221 MGI PMID:15464586 737141 Gata4 GATA binding protein 4 gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0004187 cardia bifida IAGP N RGD:5509061 20141003 MGI PMID:9136933 737141 Gata4 GATA binding protein 4 gene MP:0004225 patent cardiac foramen ovale IAGP N RGD:5509061 20141003 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0004484 abnormal response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:21746915 737141 Gata4 GATA binding protein 4 gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:21746915 737141 Gata4 GATA binding protein 4 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220602 MGI PMID:21248289 737141 Gata4 GATA binding protein 4 gene MP:0004896 abnormal endometrium morphology IAGP N RGD:5509061 20220602 MGI PMID:21248289 737141 Gata4 GATA binding protein 4 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20220602 MGI PMID:21248289 737141 Gata4 GATA binding protein 4 gene MP:0004910 decreased seminal vesicle weight IAGP N RGD:5509061 20220609 MGI PMID:30793514 737141 Gata4 GATA binding protein 4 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:16514068 737141 Gata4 GATA binding protein 4 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20160616 MGI PMID:26571399 737141 Gata4 GATA binding protein 4 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16514068 737141 Gata4 GATA binding protein 4 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20220602 MGI PMID:21248289 737141 Gata4 GATA binding protein 4 gene MP:0005221 abnormal rostral-caudal axis patterning IAGP N RGD:5509061 20141003 MGI PMID:9136932 737141 Gata4 GATA binding protein 4 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:16514068 737141 Gata4 GATA binding protein 4 gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21746915 737141 Gata4 GATA binding protein 4 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:15902305 737141 Gata4 GATA binding protein 4 gene MP:0005406 abnormal heart size IAGP N RGD:5509061 20141003 MGI PMID:21746915 737141 Gata4 GATA binding protein 4 gene MP:0005592 abnormal vascular smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17069789 737141 Gata4 GATA binding protein 4 gene MP:0006046 atrioventricular valve regurgitation IAGP N RGD:5509061 20141003 MGI PMID:15464586 737141 Gata4 GATA binding protein 4 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0006128 pulmonary valve stenosis IAGP N RGD:5509061 20141003 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:19411759 737141 Gata4 GATA binding protein 4 gene MP:0008788 abnormal fetal cardiomyocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:18400219 737141 Gata4 GATA binding protein 4 gene MP:0008825 abnormal cardiac epithelial to mesenchymal transition IAGP N RGD:5509061 20141003 MGI PMID:15902305 737141 Gata4 GATA binding protein 4 gene MP:0009008 delayed estrous cycle IAGP N RGD:5509061 20220602 MGI PMID:21248289 737141 Gata4 GATA binding protein 4 gene MP:0009328 delayed heart looping IAGP N RGD:5509061 20141003 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20220602 MGI PMID:21248289 737141 Gata4 GATA binding protein 4 gene MP:0009865 abnormal aorta smooth muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17069789 737141 Gata4 GATA binding protein 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19411759 737141 Gata4 GATA binding protein 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20220602 MGI PMID:35182466 737141 Gata4 GATA binding protein 4 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0010408 sinus venosus atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:17069789 737141 Gata4 GATA binding protein 4 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:15464586 737141 Gata4 GATA binding protein 4 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0010419 inlet ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0010422 heart right ventricle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15902305 737141 Gata4 GATA binding protein 4 gene MP:0010428 abnormal heart right ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0010429 abnormal heart left ventricle outflow tract morphology IAGP N RGD:5509061 20141003 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0010432 common ventricle IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0010432 common ventricle IAGP N RGD:5509061 20141003 MGI PMID:15902305 737141 Gata4 GATA binding protein 4 gene MP:0010454 abnormal truncus arteriosus septation IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0010463 aorta stenosis IAGP N RGD:5509061 20141003 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0010485 aortic arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0010503 myocardial trabeculae hypoplasia IAGP N RGD:5509061 20240118 MGI PMID:15464586 737141 Gata4 GATA binding protein 4 gene MP:0010541 aorta hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0010545 abnormal heart layer morphology IAGP N RGD:5509061 20141003 MGI PMID:24380800 737141 Gata4 GATA binding protein 4 gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:19411759 737141 Gata4 GATA binding protein 4 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0010561 absent coronary vessels IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0010574 dilated aorta IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0010585 abnormal conotruncal ridge morphology IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0010587 conotruncal ridge hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15902305 737141 Gata4 GATA binding protein 4 gene MP:0010587 conotruncal ridge hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0010593 thick aortic valve cusps IAGP N RGD:5509061 20231221 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0010605 thick pulmonary valve cusps IAGP N RGD:5509061 20231221 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0010640 ventricular myocardium compact layer hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20141003 MGI PMID:17069789 737141 Gata4 GATA binding protein 4 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:17069789 737141 Gata4 GATA binding protein 4 gene MP:0010975 abnormal lung lobe morphology IAGP N RGD:5509061 20160623 MGI PMID:25807280 737141 Gata4 GATA binding protein 4 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20220602 MGI PMID:35182466 737141 Gata4 GATA binding protein 4 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17069789 737141 Gata4 GATA binding protein 4 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16514068 737141 Gata4 GATA binding protein 4 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9136933 737141 Gata4 GATA binding protein 4 gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IEA N RGD:5509061 20141003 MGI 737141 Gata4 GATA binding protein 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11297508 737141 Gata4 GATA binding protein 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16847256 737141 Gata4 GATA binding protein 4 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15464586 737141 Gata4 GATA binding protein 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15902305 737141 Gata4 GATA binding protein 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24380800 737141 Gata4 GATA binding protein 4 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20220602 MGI PMID:35182466 737141 Gata4 GATA binding protein 4 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24380800 737141 Gata4 GATA binding protein 4 gene MP:0011112 lethality during fetal growth through weaning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23836893 737141 Gata4 GATA binding protein 4 gene MP:0011200 abnormal extraembryonic coelom morphology IAGP N RGD:5509061 20141003 MGI PMID:9136933 737141 Gata4 GATA binding protein 4 gene MP:0011388 absent heart IAGP N RGD:5509061 20141003 MGI PMID:18400219 737141 Gata4 GATA binding protein 4 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:22589735 737141 Gata4 GATA binding protein 4 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:24380800 737141 Gata4 GATA binding protein 4 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20240118 MGI PMID:15464586 737141 Gata4 GATA binding protein 4 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20240118 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0011673 unbalanced complete common atrioventricular canal IAGP N RGD:5509061 20210708 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0012061 abnormal diaphragm central tendon morphology IAGP N RGD:5509061 20141003 MGI PMID:17069789 737141 Gata4 GATA binding protein 4 gene MP:0012081 absent heart tube IAGP N RGD:5509061 20141003 MGI PMID:18400219 737141 Gata4 GATA binding protein 4 gene MP:0012081 absent heart tube IAGP N RGD:5509061 20141003 MGI PMID:9136932 737141 Gata4 GATA binding protein 4 gene MP:0012083 absent foregut IAGP N RGD:5509061 20141003 MGI PMID:9136933 737141 Gata4 GATA binding protein 4 gene MP:0012185 abnormal muscle precursor cell morphology IAGP N RGD:5509061 20160623 MGI PMID:25807280 737141 Gata4 GATA binding protein 4 gene MP:0012186 abnormal muscle precursor cell physiology IAGP N RGD:5509061 20160623 MGI PMID:25807280 737141 Gata4 GATA binding protein 4 gene MP:0012251 abnormal diaphragm development IAGP N RGD:5509061 20160623 MGI PMID:25807280 737141 Gata4 GATA binding protein 4 gene MP:0012278 abnormal cardiogenic mesoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:18400219 737141 Gata4 GATA binding protein 4 gene MP:0013006 abnormal enteric neural crest cell migration IAGP N RGD:5509061 20160616 MGI PMID:26571399 737141 Gata4 GATA binding protein 4 gene MP:0013603 abnormal fetal Leydig cell differentiation IAGP N RGD:5509061 20150319 MGI PMID:12223418 737141 Gata4 GATA binding protein 4 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0014515 decreased circulating anti-Mullerian hormone level IAGP N RGD:5509061 20240822 MGI PMID:21248289 737141 Gata4 GATA binding protein 4 gene MP:0020356 abnormal Sertoli cell barrier function IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220203 MGI PMID:21172404 737141 Gata4 GATA binding protein 4 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20191128 MGI PMID:15902305 737141 Gata4 GATA binding protein 4 gene MP:0030992 atrioventricular cushion hypoplasia IAGP N RGD:5509061 20191128 MGI PMID:19889636 737141 Gata4 GATA binding protein 4 gene MP:0031068 decreased blood oxygen saturation level IAGP N RGD:5509061 20200618 MGI PMID:25807280 737141 Gata4 GATA binding protein 4 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:21248289 737141 Gata4 GATA binding protein 4 gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220630 MGI PMID:21248289 737144 Aqp6 aquaporin 6 gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20220519 MGI 737144 Aqp6 aquaporin 6 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20201022 MGI 737144 Aqp6 aquaporin 6 gene MP:0011964 increased total retina thickness IEA N RGD:5509061 20210128 MGI 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0000516 abnormal renal/urinary system morphology IAGP N RGD:5509061 20160915 MGI PMID:25188265 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0001194 dermatitis IAGP N RGD:5509061 20160915 MGI PMID:25188265 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0001265 decreased body size IAGP N RGD:5509061 20160915 MGI PMID:25188265 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0001499 abnormal kindling response IAGP N RGD:5509061 20141003 MGI PMID:19763161 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20141003 MGI PMID:19763161 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0001970 abnormal pain threshold IAGP N RGD:5509061 20141003 MGI PMID:15314237 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:15314237 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20160915 MGI PMID:25188265 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0002193 minimal clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:19763161 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20230511 MGI PMID:33323889 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0002734 abnormal mechanical nociception IAGP N RGD:5509061 20160915 MGI PMID:25188265 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:15314237 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20160915 MGI PMID:25188265 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20160915 MGI PMID:25188265 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0003468 increased single cell response intensity IAGP N RGD:5509061 20230511 MGI PMID:33323889 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0003631 nervous system phenotype IAGP N RGD:5509061 20230511 MGI PMID:33323889 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20160915 MGI PMID:25188265 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0004512 anosmia IAGP N RGD:5509061 20160915 MGI PMID:25188265 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0005386 behavior/neurological phenotype IAGP N RGD:5509061 20230511 MGI PMID:33323889 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20160915 MGI PMID:25188265 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20230511 MGI PMID:33323889 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0008531 increased chemical nociceptive threshold IAGP N RGD:5509061 20160915 MGI PMID:25188265 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20111116 MGI 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20160915 MGI PMID:25188265 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15314237 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20160915 MGI PMID:25188265 737152 Scn9a sodium channel, voltage-gated, type IX, alpha gene MP:0011089 perinatal lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:20628201 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0001330 abnormal optic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15102918 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:15102918 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:17868089 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15102918 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:17868089 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20628201 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:15102918 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:17868089 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0002064 seizures IAGP N RGD:5509061 20141003 MGI PMID:20628201 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:20628201 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17868089 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:20628201 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:15102918 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20141003 MGI PMID:20628201 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:20628201 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:15102918 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:20628201 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:15102918 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0009358 environmentally induced seizures IAGP N RGD:5509061 20141003 MGI PMID:20628201 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0011083 lethality at weaning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15102918 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17868089 737154 Scn1b sodium channel, voltage-gated, type I, beta gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 737156 Foxo1 forkhead box O1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18590693 737156 Foxo1 forkhead box O1 gene MP:0000187 abnormal triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18590693 737156 Foxo1 forkhead box O1 gene MP:0000263 absent organized vascular network IAGP N RGD:5509061 20141003 MGI PMID:15184386 737156 Foxo1 forkhead box O1 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0000291 enlarged pericardium IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0000292 distended pericardium IAGP N RGD:5509061 20141003 MGI PMID:14978268 737156 Foxo1 forkhead box O1 gene MP:0000687 small lymphoid organs IAGP N RGD:5509061 20141003 MGI PMID:19658095 737156 Foxo1 forkhead box O1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:23135404 737156 Foxo1 forkhead box O1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:19658095 737156 Foxo1 forkhead box O1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19285438 737156 Foxo1 forkhead box O1 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23135404 737156 Foxo1 forkhead box O1 gene MP:0000753 paralysis IAGP N RGD:5509061 20141003 MGI PMID:23135404 737156 Foxo1 forkhead box O1 gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20160811 MGI PMID:26061565 737156 Foxo1 forkhead box O1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 737156 Foxo1 forkhead box O1 gene MP:0001505 hunched posture IAGP N RGD:5509061 20141003 MGI PMID:23135404 737156 Foxo1 forkhead box O1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20150618 MGI PMID:25264246 737156 Foxo1 forkhead box O1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:17254969 737156 Foxo1 forkhead box O1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0001691 abnormal somite shape IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0001718 abnormal visceral yolk sac morphology IAGP N RGD:5509061 20141003 MGI PMID:15184386 737156 Foxo1 forkhead box O1 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:14978268 737156 Foxo1 forkhead box O1 gene MP:0001749 suppressed circulating follicle stimulating hormone level IAGP N RGD:5509061 20160811 MGI PMID:26061565 737156 Foxo1 forkhead box O1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:19285438 737156 Foxo1 forkhead box O1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:23135404 737156 Foxo1 forkhead box O1 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20160811 MGI PMID:26061565 737156 Foxo1 forkhead box O1 gene MP:0002020 increased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 737156 Foxo1 forkhead box O1 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 737156 Foxo1 forkhead box O1 gene MP:0002047 increased hepatic hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 737156 Foxo1 forkhead box O1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20150618 MGI PMID:25264246 737156 Foxo1 forkhead box O1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:16642023 737156 Foxo1 forkhead box O1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:12219087 737156 Foxo1 forkhead box O1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17254969 737156 Foxo1 forkhead box O1 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23135404 737156 Foxo1 forkhead box O1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:23135404 737156 Foxo1 forkhead box O1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15489287 737156 Foxo1 forkhead box O1 gene MP:0002189 abnormal myocardial trabeculae morphology IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19285438 737156 Foxo1 forkhead box O1 gene MP:0002590 increased mean corpuscular volume IEA N RGD:5509061 20220811 MGI 737156 Foxo1 forkhead box O1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:18590693 737156 Foxo1 forkhead box O1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:16642023 737156 Foxo1 forkhead box O1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:18590693 737156 Foxo1 forkhead box O1 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20150618 MGI PMID:25264246 737156 Foxo1 forkhead box O1 gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20160811 MGI PMID:26061565 737156 Foxo1 forkhead box O1 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20220811 MGI 737156 Foxo1 forkhead box O1 gene MP:0002947 increased hemangioma incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 737156 Foxo1 forkhead box O1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20150618 MGI PMID:25264246 737156 Foxo1 forkhead box O1 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20150618 MGI PMID:25264246 737156 Foxo1 forkhead box O1 gene MP:0003645 increased pancreatic beta cell number IAGP N RGD:5509061 20141003 MGI PMID:16642023 737156 Foxo1 forkhead box O1 gene MP:0003667 increased hemangiosarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 737156 Foxo1 forkhead box O1 gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15184386 737156 Foxo1 forkhead box O1 gene MP:0003976 decreased circulating VLDL triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15184386 737156 Foxo1 forkhead box O1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:15184386 737156 Foxo1 forkhead box O1 gene MP:0004086 absent heartbeat IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19285438 737156 Foxo1 forkhead box O1 gene MP:0004762 increased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:19285438 737156 Foxo1 forkhead box O1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15184386 737156 Foxo1 forkhead box O1 gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0004794 increased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:19285438 737156 Foxo1 forkhead box O1 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23135404 737156 Foxo1 forkhead box O1 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:23135404 737156 Foxo1 forkhead box O1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20141003 MGI PMID:19879843 737156 Foxo1 forkhead box O1 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23135404 737156 Foxo1 forkhead box O1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19285438 737156 Foxo1 forkhead box O1 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19658095 737156 Foxo1 forkhead box O1 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19658095 737156 Foxo1 forkhead box O1 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19658095 737156 Foxo1 forkhead box O1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:18590693 737156 Foxo1 forkhead box O1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20160811 MGI PMID:26061565 737156 Foxo1 forkhead box O1 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:18590693 737156 Foxo1 forkhead box O1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20150618 MGI PMID:25264246 737156 Foxo1 forkhead box O1 gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:15184386 737156 Foxo1 forkhead box O1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 737156 Foxo1 forkhead box O1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19285438 737156 Foxo1 forkhead box O1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23135404 737156 Foxo1 forkhead box O1 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20160811 MGI PMID:26061565 737156 Foxo1 forkhead box O1 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19285438 737156 Foxo1 forkhead box O1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12219087 737156 Foxo1 forkhead box O1 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16642023 737156 Foxo1 forkhead box O1 gene MP:0005655 increased aggression IEA N RGD:5509061 20240523 MGI 737156 Foxo1 forkhead box O1 gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0005666 abnormal adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20150618 MGI PMID:25264246 737156 Foxo1 forkhead box O1 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15184386 737156 Foxo1 forkhead box O1 gene MP:0006341 small first pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:15184386 737156 Foxo1 forkhead box O1 gene MP:0006345 absent second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19658095 737156 Foxo1 forkhead box O1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23135404 737156 Foxo1 forkhead box O1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19658095 737156 Foxo1 forkhead box O1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23135404 737156 Foxo1 forkhead box O1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:19658095 737156 Foxo1 forkhead box O1 gene MP:0008081 abnormal single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19658095 737156 Foxo1 forkhead box O1 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:19285438 737156 Foxo1 forkhead box O1 gene MP:0008183 absent marginal zone B cells IAGP N RGD:5509061 20141003 MGI PMID:19879843 737156 Foxo1 forkhead box O1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:19285438 737156 Foxo1 forkhead box O1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:23135404 737156 Foxo1 forkhead box O1 gene MP:0008868 abnormal granulosa cell morphology IAGP N RGD:5509061 20220331 MGI PMID:26061565 737156 Foxo1 forkhead box O1 gene MP:0008964 decreased carbon dioxide production IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0009175 abnormal pancreatic beta cell differentiation IAGP N RGD:5509061 20150618 MGI PMID:25264246 737156 Foxo1 forkhead box O1 gene MP:0009328 delayed heart looping IAGP N RGD:5509061 20141003 MGI PMID:14978268 737156 Foxo1 forkhead box O1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0009542 decreased thymocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19658095 737156 Foxo1 forkhead box O1 gene MP:0009931 abnormal skin appearance IAGP N RGD:5509061 20141003 MGI PMID:23135404 737156 Foxo1 forkhead box O1 gene MP:0010026 decreased liver cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0010306 increased hamartoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17254969 737156 Foxo1 forkhead box O1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20191226 MGI PMID:12219087 737156 Foxo1 forkhead box O1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15489287 737156 Foxo1 forkhead box O1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14978268 737156 Foxo1 forkhead box O1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15184386 737156 Foxo1 forkhead box O1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17254969 737156 Foxo1 forkhead box O1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:22055502 737156 Foxo1 forkhead box O1 gene MP:0012253 abnormal intersomitic vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:14978268 737156 Foxo1 forkhead box O1 gene MP:0012411 increased granulosa cell tumor incidence IAGP N RGD:5509061 20160811 MGI PMID:26061565 737156 Foxo1 forkhead box O1 gene MP:0012492 pharyngeal arch artery hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15184386 737156 Foxo1 forkhead box O1 gene MP:0012730 abnormal internal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:14978268 737156 Foxo1 forkhead box O1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210520 MGI 737160 Shc3 src homology 2 domain-containing transforming protein C3 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:11163269 737160 Shc3 src homology 2 domain-containing transforming protein C3 gene MP:0000964 small dorsal root ganglion IAGP N RGD:5509061 20141003 MGI PMID:11163269 737160 Shc3 src homology 2 domain-containing transforming protein C3 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:11163269 737160 Shc3 src homology 2 domain-containing transforming protein C3 gene MP:0000969 abnormal nociceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:11163269 737160 Shc3 src homology 2 domain-containing transforming protein C3 gene MP:0001015 small superior cervical ganglion IAGP N RGD:5509061 20141003 MGI PMID:11163269 737170 Ppm1f protein phosphatase 1F (PP2C domain containing) gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 737170 Ppm1f protein phosphatase 1F (PP2C domain containing) gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 737170 Ppm1f protein phosphatase 1F (PP2C domain containing) gene MP:0031391 increased locomotor activity IEA N RGD:5509061 20220421 MGI 737173 Nid1 nidogen 1 gene MP:0000951 sporadic seizures IAGP N RGD:5509061 20141003 MGI PMID:12480912 737173 Nid1 nidogen 1 gene MP:0001303 abnormal lens morphology IAGP N RGD:5509061 20141003 MGI PMID:12480912 737173 Nid1 nidogen 1 gene MP:0001961 abnormal reflex IAGP N RGD:5509061 20141003 MGI PMID:12480912 737173 Nid1 nidogen 1 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:12480912 737173 Nid1 nidogen 1 gene MP:0003658 abnormal capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:12480912 737173 Nid1 nidogen 1 gene MP:0004272 abnormal basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12480912 737173 Nid1 nidogen 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:17008882 737175 Pigm phosphatidylinositol glycan anchor biosynthesis, class M gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210422 MGI 737175 Pigm phosphatidylinositol glycan anchor biosynthesis, class M gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210422 MGI 737175 Pigm phosphatidylinositol glycan anchor biosynthesis, class M gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20221103 MGI 737177 Slc27a2 solute carrier family 27 (fatty acid transporter), member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12719378 737177 Slc27a2 solute carrier family 27 (fatty acid transporter), member 2 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:12719378 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0000371 diluted coat color IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0001577 anemia IEA N RGD:5509061 20111116 MGI 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20150702 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20150702 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20150702 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20150702 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0003131 increased erythrocyte cell number IAGP N RGD:5509061 20150702 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0004201 fetal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20150702 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20150702 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0005639 hemosiderosis IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0008810 increased circulating iron level IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0009429 decreased embryo weight IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20150702 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0011179 decreased erythroblast number IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0011246 abnormal fetal liver hematopoietic progenitor cell morphology IAGP N RGD:5509061 20150702 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20150625 MGI PMID:25552701 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0011400 lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22363754 737178 Picalm phosphatidylinositol binding clathrin assembly protein gene MP:0014263 decreased spleen B cell follicle number IAGP N RGD:5509061 20230706 MGI PMID:22363754 737179 Eif2ak1 eukaryotic translation initiation factor 2 alpha kinase 1 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11726526 737179 Eif2ak1 eukaryotic translation initiation factor 2 alpha kinase 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:11726526 737179 Eif2ak1 eukaryotic translation initiation factor 2 alpha kinase 1 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:11726526 737179 Eif2ak1 eukaryotic translation initiation factor 2 alpha kinase 1 gene MP:0001589 abnormal mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:11726526 737179 Eif2ak1 eukaryotic translation initiation factor 2 alpha kinase 1 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:11726526 737179 Eif2ak1 eukaryotic translation initiation factor 2 alpha kinase 1 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:11726526 737179 Eif2ak1 eukaryotic translation initiation factor 2 alpha kinase 1 gene MP:0002811 macrocytic anemia IAGP N RGD:5509061 20141003 MGI PMID:11726526 737179 Eif2ak1 eukaryotic translation initiation factor 2 alpha kinase 1 gene MP:0003656 abnormal erythrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11726526 737179 Eif2ak1 eukaryotic translation initiation factor 2 alpha kinase 1 gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 737179 Eif2ak1 eukaryotic translation initiation factor 2 alpha kinase 1 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11726526 737179 Eif2ak1 eukaryotic translation initiation factor 2 alpha kinase 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20201022 MGI 737179 Eif2ak1 eukaryotic translation initiation factor 2 alpha kinase 1 gene MP:0011171 increased number of Heinz bodies IAGP N RGD:5509061 20141003 MGI PMID:11726526 737179 Eif2ak1 eukaryotic translation initiation factor 2 alpha kinase 1 gene MP:0031085 increased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:11726526 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0000523 cortical renal glomerulopathies IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0000533 kidney hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:17164266 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:17164266 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17164266 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20220811 MGI 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0001297 microphthalmia IEA N RGD:5509061 20210826 MGI 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0001711 abnormal placenta morphology IEA N RGD:5509061 20210826 MGI 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0001785 edema IEA N RGD:5509061 20210826 MGI 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:22253810 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20240328 MGI PMID:38237079 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17164266 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22253810 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:17164266 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:22253810 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20210520 MGI 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0002269 muscular atrophy IAGP N RGD:5509061 20141003 MGI PMID:17164266 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:17164266 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0002699 abnormal vitreous body morphology IEA N RGD:5509061 20240523 MGI 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0002703 abnormal renal tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:22253810 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0002828 abnormal renal glomerular capsule morphology IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:22253810 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17164266 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0003606 kidney failure IAGP N RGD:5509061 20141003 MGI PMID:22253810 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210826 MGI 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0004969 pale kidney IAGP N RGD:5509061 20141003 MGI PMID:22253810 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:22253810 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:17164266 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0006054 spinal hemorrhage IAGP N RGD:5509061 20240328 MGI PMID:38237079 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0008062 abnormal podocyte slit junction morphology IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:22253810 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220811 MGI 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:17164266 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0009413 skeletal muscle fiber atrophy IAGP N RGD:5509061 20141003 MGI PMID:17164266 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0009546 absent gastric milk in neonates IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0010090 increased circulating creatine kinase level IAGP N RGD:5509061 20141003 MGI PMID:17164266 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20210128 MGI 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0011107 embryonic lethality between somite formation and embryo turning, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11929971 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11929971 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0011290 decreased nephron number IAGP N RGD:5509061 20141003 MGI PMID:22253810 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0011294 renal glomerulus hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:22253810 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0011348 abnormal renal glomerulus basement membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:17549255 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:22253810 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:22253810 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0012732 abnormal perineural vascular plexus morphology IAGP N RGD:5509061 20240328 MGI PMID:38237079 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20220811 MGI 737180 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase gene MP:0014257 embryonic lethality prior to tooth bud stage, complete penetrance IAGP N RGD:5509061 20240328 MGI PMID:38237079 737183 Zfp36 zinc finger protein 36 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:14769925 737183 Zfp36 zinc finger protein 36 gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20141106 MGI PMID:24727475 737183 Zfp36 zinc finger protein 36 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141106 MGI PMID:24727475 737183 Zfp36 zinc finger protein 36 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141106 MGI PMID:24727475 737183 Zfp36 zinc finger protein 36 gene MP:0000414 alopecia IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0001492 abnormal pilomotor reflex IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0001613 abnormal vasodilation IAGP N RGD:5509061 20141106 MGI PMID:24727475 737183 Zfp36 zinc finger protein 36 gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:14769925 737183 Zfp36 zinc finger protein 36 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0001852 conjunctivitis IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0001853 heart inflammation IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0001863 blood vessel inflammation IAGP N RGD:5509061 20141106 MGI PMID:24727475 737183 Zfp36 zinc finger protein 36 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20160310 MGI PMID:26831084 737183 Zfp36 zinc finger protein 36 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0002371 abnormal thymus cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0002375 abnormal thymus medulla morphology IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:14769925 737183 Zfp36 zinc finger protein 36 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20181227 MGI 737183 Zfp36 zinc finger protein 36 gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141106 MGI PMID:24727475 737183 Zfp36 zinc finger protein 36 gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:14769925 737183 Zfp36 zinc finger protein 36 gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0003436 decreased susceptibility to induced arthritis IAGP N RGD:5509061 20160310 MGI PMID:26831084 737183 Zfp36 zinc finger protein 36 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141106 MGI PMID:24727475 737183 Zfp36 zinc finger protein 36 gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141106 MGI PMID:24727475 737183 Zfp36 zinc finger protein 36 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20160310 MGI PMID:26831084 737183 Zfp36 zinc finger protein 36 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141106 MGI PMID:24727475 737183 Zfp36 zinc finger protein 36 gene MP:0005202 lethargy IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0005426 tachypnea IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20141106 MGI PMID:24727475 737183 Zfp36 zinc finger protein 36 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0008412 increased cellular sensitivity to oxidative stress IAGP N RGD:5509061 20141106 MGI PMID:24727475 737183 Zfp36 zinc finger protein 36 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0008843 absent subcutaneous adipose tissue IAGP N RGD:5509061 20141003 MGI PMID:8630730 737183 Zfp36 zinc finger protein 36 gene MP:0010373 myeloid hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:16983719 737183 Zfp36 zinc finger protein 36 gene MP:0010922 alveolitis IAGP N RGD:5509061 20141003 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210211 MGI PMID:22491258 737183 Zfp36 zinc finger protein 36 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20201022 MGI 737184 Kynu kynureninase gene MP:0000111 cleft palate IAGP N RGD:5509061 20190502 MGI PMID:28792876 737184 Kynu kynureninase gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20190502 MGI PMID:28792876 737184 Kynu kynureninase gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20190502 MGI PMID:28792876 737184 Kynu kynureninase gene MP:0000564 syndactyly IAGP N RGD:5509061 20190502 MGI PMID:28792876 737184 Kynu kynureninase gene MP:0000576 clubfoot IAGP N RGD:5509061 20190502 MGI PMID:28792876 737184 Kynu kynureninase gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 737184 Kynu kynureninase gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20211021 MGI 737184 Kynu kynureninase gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 737184 Kynu kynureninase gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20190502 MGI PMID:28792876 737184 Kynu kynureninase gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 737184 Kynu kynureninase gene MP:0002989 small kidney IAGP N RGD:5509061 20190502 MGI PMID:28792876 737184 Kynu kynureninase gene MP:0003718 maternal effect IAGP N RGD:5509061 20190502 MGI PMID:28792876 737184 Kynu kynureninase gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20220811 MGI 737184 Kynu kynureninase gene MP:0013242 abnormal amino acid metabolism IAGP N RGD:5509061 20190418 MGI PMID:28792876 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12388241 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7724593 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9466969 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:9466969 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10432390 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000530 abnormal kidney vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:9466969 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000818 abnormal amygdala morphology IAGP N RGD:5509061 20141003 MGI PMID:11384784 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0000832 abnormal thalamus morphology IAGP N RGD:5509061 20141003 MGI PMID:11384784 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0001586 abnormal erythrocyte cell number IEA N RGD:5509061 20210128 MGI 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0001589 abnormal mean corpuscular hemoglobin IEA N RGD:5509061 20211021 MGI 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:15087458 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:15306694 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0001596 hypotension IAGP N RGD:5509061 20141003 MGI PMID:7642517 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0001629 abnormal heart rate IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20200514 MGI 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0002136 abnormal kidney physiology IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0002593 high mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0002596 abnormal hematocrit IEA N RGD:5509061 20210128 MGI 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0002829 abnormal juxtaglomerular apparatus morphology IAGP N RGD:5509061 20141003 MGI PMID:8878439 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0002834 decreased heart weight IAGP N RGD:5509061 20141003 MGI PMID:9466969 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9466969 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7724593 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0002843 decreased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:9466969 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:15306694 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0003211 abnormal aorta elastic fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21252156 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0003352 increased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:7642517 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0003353 decreased circulating renin level IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0003620 oliguria IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:15306694 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0003918 decreased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0003985 renal fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0004193 abnormal kidney papilla morphology IAGP N RGD:5509061 20141003 MGI PMID:9466969 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0004952 increased spleen weight IEA N RGD:5509061 20210128 MGI 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20200416 MGI PMID:16001071 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0005528 decreased renal glomerular filtration rate IAGP N RGD:5509061 20141003 MGI PMID:21459331 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0005563 abnormal hemoglobin content IEA N RGD:5509061 20210128 MGI 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0005564 increased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0005582 increased renin activity IAGP N RGD:5509061 20141003 MGI PMID:7642517 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0005583 decreased renin activity IAGP N RGD:5509061 20141003 MGI PMID:15306694 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0005618 decreased urine potassium level IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:12388241 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21459331 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7642517 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:7724593 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0008055 increased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0008528 polycystic kidney IEA N RGD:5509061 20210520 MGI 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0009118 increased white fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22919058 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0009131 decreased white fat cell number IAGP N RGD:5509061 20141003 MGI PMID:22919058 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:21252156 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0010066 abnormal red blood cell distribution width IEA N RGD:5509061 20211021 MGI 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0010108 abnormal renal water reabsorption IAGP N RGD:5509061 20141003 MGI PMID:21459331 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9466969 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9466969 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0010420 muscular ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9466969 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0010996 increased aorta wall thickness IAGP N RGD:5509061 20141009 MGI PMID:23636094 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0010997 decreased aorta wall thickness IAGP N RGD:5509061 20141003 MGI PMID:21252156 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9466969 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0011167 abnormal adipose tissue development IAGP N RGD:5509061 20141003 MGI PMID:22919058 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0011301 juxtaglomerular cell hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8878439 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0011305 dilated kidney calyx IAGP N RGD:5509061 20141003 MGI PMID:9466969 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0011306 absent kidney pelvis IAGP N RGD:5509061 20141003 MGI PMID:10432390 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0011316 abnormal kidney interlobular artery morphology IAGP N RGD:5509061 20141003 MGI PMID:8878439 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0011363 renal glomerulus atrophy IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0011425 abnormal kidney interstitium morphology IAGP N RGD:5509061 20141003 MGI PMID:11292619 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:18497303 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0011565 kidney papillary hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9466969 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0011898 abnormal platelet cell number IEA N RGD:5509061 20211021 MGI 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:12388241 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0031231 decreased circulating angiotensin II level IAGP N RGD:5509061 20210204 MGI PMID:17607364 737190 Agtr1a angiotensin II receptor, type 1a gene MP:0031273 decreased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:21252156 737192 Sstr1 somatostatin receptor 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20111116 MGI 737192 Sstr1 somatostatin receptor 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20111116 MGI 737192 Sstr1 somatostatin receptor 1 gene MP:0004495 decreased synaptic glutamate release IAGP N RGD:5509061 20141003 MGI PMID:17425570 737192 Sstr1 somatostatin receptor 1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:15548214 737192 Sstr1 somatostatin receptor 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20111116 MGI 737192 Sstr1 somatostatin receptor 1 gene MP:0005551 abnormal eye electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:15464758 737192 Sstr1 somatostatin receptor 1 gene MP:0006072 abnormal retina apoptosis IAGP N RGD:5509061 20141003 MGI PMID:17425570 737192 Sstr1 somatostatin receptor 1 gene MP:0006074 abnormal retina rod bipolar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:14750962 737192 Sstr1 somatostatin receptor 1 gene MP:0020421 increased freezing behavior IEA N RGD:5509061 20231207 MGI 737196 Junb jun B proto-oncogene gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:14769860 737196 Junb jun B proto-oncogene gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:14769860 737196 Junb jun B proto-oncogene gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:14769860 737196 Junb jun B proto-oncogene gene MP:0001193 psoriasis IAGP N RGD:5509061 20141003 MGI PMID:16163348 737196 Junb jun B proto-oncogene gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0001200 thick skin IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0001209 spontaneous skin ulceration IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:16163348 737196 Junb jun B proto-oncogene gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:16163348 737196 Junb jun B proto-oncogene gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:14769860 737196 Junb jun B proto-oncogene gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16163348 737196 Junb jun B proto-oncogene gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 737196 Junb jun B proto-oncogene gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20190502 MGI 737196 Junb jun B proto-oncogene gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16163348 737196 Junb jun B proto-oncogene gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0002060 abnormal skin morphology IAGP N RGD:5509061 20141003 MGI PMID:16163348 737196 Junb jun B proto-oncogene gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:14769860 737196 Junb jun B proto-oncogene gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0002151 abnormal neural tube morphology IEA N RGD:5509061 20190502 MGI 737196 Junb jun B proto-oncogene gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:14769860 737196 Junb jun B proto-oncogene gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0002989 small kidney IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0002993 autoimmune arthritis IAGP N RGD:5509061 20141003 MGI PMID:16163348 737196 Junb jun B proto-oncogene gene MP:0003232 abnormal forebrain development IEA N RGD:5509061 20190502 MGI 737196 Junb jun B proto-oncogene gene MP:0003427 parakeratosis IAGP N RGD:5509061 20141003 MGI PMID:16163348 737196 Junb jun B proto-oncogene gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20190502 MGI 737196 Junb jun B proto-oncogene gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:16163348 737196 Junb jun B proto-oncogene gene MP:0003864 abnormal midbrain development IEA N RGD:5509061 20190502 MGI 737196 Junb jun B proto-oncogene gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 737196 Junb jun B proto-oncogene gene MP:0004796 increased anti-histone antibody level IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0004801 increased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:16163348 737196 Junb jun B proto-oncogene gene MP:0004947 skin inflammation IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0004952 increased spleen weight IEA N RGD:5509061 20220811 MGI 737196 Junb jun B proto-oncogene gene MP:0004970 kidney atrophy IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:14769860 737196 Junb jun B proto-oncogene gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:14769860 737196 Junb jun B proto-oncogene gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:14769860 737196 Junb jun B proto-oncogene gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:14769860 737196 Junb jun B proto-oncogene gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:14769860 737196 Junb jun B proto-oncogene gene MP:0005481 increased chronic myelocytic leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:14769860 737196 Junb jun B proto-oncogene gene MP:0006108 abnormal hindbrain development IEA N RGD:5509061 20190502 MGI 737196 Junb jun B proto-oncogene gene MP:0008097 increased plasma cell number IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:14769860 737196 Junb jun B proto-oncogene gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:14769860 737196 Junb jun B proto-oncogene gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0010971 abnormal periosteum morphology IAGP N RGD:5509061 20141003 MGI PMID:16163348 737196 Junb jun B proto-oncogene gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737196 Junb jun B proto-oncogene gene MP:0011159 abnormal epidermal-dermal junction morphology IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0011405 tubulointerstitial nephritis IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0011409 increased renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0011567 increased renal glomerulus lobularity IAGP N RGD:5509061 20141003 MGI PMID:19918056 737196 Junb jun B proto-oncogene gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 737196 Junb jun B proto-oncogene gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:19918056 737198 Sftpb surfactant associated protein B gene MP:0001177 atelectasis IAGP N RGD:5509061 20141003 MGI PMID:7644495 737198 Sftpb surfactant associated protein B gene MP:0001385 pup cannibalization IAGP N RGD:5509061 20141003 MGI PMID:7644495 737198 Sftpb surfactant associated protein B gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:7644495 737198 Sftpb surfactant associated protein B gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:7644495 737198 Sftpb surfactant associated protein B gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:7644495 737198 Sftpb surfactant associated protein B gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:7644495 737198 Sftpb surfactant associated protein B gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:7644495 737198 Sftpb surfactant associated protein B gene MP:0002275 abnormal type II pneumocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:7644495 737198 Sftpb surfactant associated protein B gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:10502556 737198 Sftpb surfactant associated protein B gene MP:0004780 abnormal surfactant secretion IAGP N RGD:5509061 20141003 MGI PMID:7644495 737198 Sftpb surfactant associated protein B gene MP:0004781 abnormal surfactant composition IAGP N RGD:5509061 20141003 MGI PMID:7644495 737198 Sftpb surfactant associated protein B gene MP:0004782 abnormal surfactant physiology IAGP N RGD:5509061 20141003 MGI PMID:7644495 737198 Sftpb surfactant associated protein B gene MP:0005165 increased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:10502556 737198 Sftpb surfactant associated protein B gene MP:0010814 absent alveolar lamellar bodies IAGP N RGD:5509061 20141003 MGI PMID:7644495 737198 Sftpb surfactant associated protein B gene MP:0010896 decreased lung compliance IAGP N RGD:5509061 20141003 MGI PMID:10502556 737198 Sftpb surfactant associated protein B gene MP:0010938 decreased total lung capacity IAGP N RGD:5509061 20141003 MGI PMID:10502556 737198 Sftpb surfactant associated protein B gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7644495 737199 Sec31a SEC31 homolog A, COPII coat complex component gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210520 MGI 737199 Sec31a SEC31 homolog A, COPII coat complex component gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20211021 MGI 737199 Sec31a SEC31 homolog A, COPII coat complex component gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210826 MGI 737199 Sec31a SEC31 homolog A, COPII coat complex component gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20211021 MGI 737199 Sec31a SEC31 homolog A, COPII coat complex component gene MP:0010052 increased grip strength IEA N RGD:5509061 20210128 MGI 737199 Sec31a SEC31 homolog A, COPII coat complex component gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IAGP N RGD:5509061 20240808 MGI PMID:38400880 737199 Sec31a SEC31 homolog A, COPII coat complex component gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230601 MGI 737199 Sec31a SEC31 homolog A, COPII coat complex component gene MP:0013278 decreased fasting circulating glucose level IEA N RGD:5509061 20210128 MGI 737199 Sec31a SEC31 homolog A, COPII coat complex component gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20210128 MGI 737199 Sec31a SEC31 homolog A, COPII coat complex component gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20210128 MGI 737200 Hgfac hepatocyte growth factor activator gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15521012 737200 Hgfac hepatocyte growth factor activator gene MP:0031319 impaired intestine regeneration IAGP N RGD:5509061 20211125 MGI PMID:15521012 737201 Prss2 serine protease 2 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 737201 Prss2 serine protease 2 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20221215 MGI 737201 Prss2 serine protease 2 gene MP:0001513 limb grasping IEA N RGD:5509061 20210128 MGI 737201 Prss2 serine protease 2 gene MP:0001523 impaired righting response IEA N RGD:5509061 20210128 MGI 737201 Prss2 serine protease 2 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 737203 Fxyd1 FXYD domain-containing ion transport regulator 1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15563542 737203 Fxyd1 FXYD domain-containing ion transport regulator 1 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15563542 737203 Fxyd1 FXYD domain-containing ion transport regulator 1 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:15563542 737203 Fxyd1 FXYD domain-containing ion transport regulator 1 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15563542 737206 Sry sex determining region of Chr Y gene MP:0001131 abnormal ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:24190364 737206 Sry sex determining region of Chr Y gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19753101 737206 Sry sex determining region of Chr Y gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:8951075 737206 Sry sex determining region of Chr Y gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15020475 737206 Sry sex determining region of Chr Y gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:24190364 737206 Sry sex determining region of Chr Y gene MP:0001939 secondary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:7089579 737206 Sry sex determining region of Chr Y gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:7089579 737206 Sry sex determining region of Chr Y gene MP:0002212 abnormal secondary sex determination IAGP N RGD:5509061 20141003 MGI PMID:7089579 737206 Sry sex determining region of Chr Y gene MP:0002213 true hermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:7089579 737206 Sry sex determining region of Chr Y gene MP:0002213 true hermaphroditism IAGP N RGD:5509061 20141003 MGI PMID:8951075 737206 Sry sex determining region of Chr Y gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:15051956 737206 Sry sex determining region of Chr Y gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:19753101 737206 Sry sex determining region of Chr Y gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:23102580 737206 Sry sex determining region of Chr Y gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:24190364 737206 Sry sex determining region of Chr Y gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:7089579 737206 Sry sex determining region of Chr Y gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20141003 MGI PMID:9499427 737206 Sry sex determining region of Chr Y gene MP:0002996 ovotestis IAGP N RGD:5509061 20141003 MGI PMID:19753101 737206 Sry sex determining region of Chr Y gene MP:0002996 ovotestis IAGP N RGD:5509061 20141003 MGI PMID:23102580 737206 Sry sex determining region of Chr Y gene MP:0002996 ovotestis IAGP N RGD:5509061 20141003 MGI PMID:7089579 737206 Sry sex determining region of Chr Y gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:23102580 737206 Sry sex determining region of Chr Y gene MP:0004852 decreased testis weight IEA N RGD:5509061 20111116 MGI 737206 Sry sex determining region of Chr Y gene MP:0005180 abnormal circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:24190364 737206 Sry sex determining region of Chr Y gene MP:0005652 sex reversal IAGP N RGD:5509061 20141003 MGI PMID:8951075 737206 Sry sex determining region of Chr Y gene MP:0005652 sex reversal IAGP N RGD:5509061 20141003 MGI PMID:9383069 737206 Sry sex determining region of Chr Y gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20141003 MGI PMID:15020475 737206 Sry sex determining region of Chr Y gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20141003 MGI PMID:24190364 737206 Sry sex determining region of Chr Y gene MP:0009205 abnormal internal male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:8951075 737206 Sry sex determining region of Chr Y gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8951075 737206 Sry sex determining region of Chr Y gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:24190364 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0000505 decreased digestive secretion IAGP N RGD:5509061 20141003 MGI PMID:15691866 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0000519 hydronephrosis IAGP N RGD:5509061 20141003 MGI PMID:10944224 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0000538 abnormal urinary bladder morphology IAGP N RGD:5509061 20141003 MGI PMID:10944224 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:10944224 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0000539 distended urinary bladder IAGP N RGD:5509061 20141003 MGI PMID:12486155 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:10944224 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:15146045 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11959688 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11961069 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0000740 impaired smooth muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12486155 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0000741 impaired contractility of urinary bladder detrusor smooth muscle IAGP N RGD:5509061 20141003 MGI PMID:10944224 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0000742 impaired contractility of ileal smooth muscle IAGP N RGD:5509061 20141003 MGI PMID:10944224 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0000742 impaired contractility of ileal smooth muscle IAGP N RGD:5509061 20141003 MGI PMID:12486155 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:10944224 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11242080 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11959688 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15220195 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:11242080 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10944224 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:11959688 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12486155 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11242080 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0002133 abnormal respiratory system physiology IAGP N RGD:5509061 20141003 MGI PMID:11959688 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0002503 abnormal histamine physiology IAGP N RGD:5509061 20141003 MGI PMID:15691866 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:10944224 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:12486155 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11242080 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0002696 decreased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:15220195 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0002711 decreased glucagon secretion IAGP N RGD:5509061 20141003 MGI PMID:15220195 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11242080 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:15220195 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:11242080 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0002945 abnormal inhibitory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12859343 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:15220195 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:16753580 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0003194 abnormal frequency of paradoxical sleep IAGP N RGD:5509061 20141003 MGI PMID:16110248 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:16110248 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0005085 abnormal gallbladder physiology IAGP N RGD:5509061 20141003 MGI PMID:11961069 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:15220195 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:16753580 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:11242080 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:15220195 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19752163 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:15130910 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11242080 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0006243 impaired pupillary reflex IAGP N RGD:5509061 20160929 MGI PMID:27534441 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11242080 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:20439723 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:20439723 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0010386 abnormal urinary bladder physiology IAGP N RGD:5509061 20141003 MGI PMID:11959688 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:11242080 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:15146045 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0012125 decreased bronchoconstrictive response IAGP N RGD:5509061 20141003 MGI PMID:14645675 737208 Chrm3 cholinergic receptor, muscarinic 3, cardiac gene MP:0013300 abnormal submandibular gland physiology IAGP N RGD:5509061 20141225 MGI PMID:15146045 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0000061 fragile skeleton IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0000097 short maxilla IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0000134 abnormal compact bone thickness IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0000161 scoliosis IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20111116 MGI 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20111116 MGI 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0000372 irregular coat pigmentation IEA N RGD:5509061 20190530 MGI 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0001674 abnormal germ layer development IAGP N RGD:5509061 20141003 MGI PMID:11431694 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0001923 reduced female fertility IEA N RGD:5509061 20111116 MGI 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:19202076 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11717426 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0002411 decreased susceptibility to bacterial infection IEA N RGD:5509061 20111116 MGI 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11717426 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0004965 inner cell mass degeneration IAGP N RGD:5509061 20141003 MGI PMID:11431694 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0005079 decreased cytotoxic T cell cytolysis IEA N RGD:5509061 20111116 MGI 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11717426 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0005342 abnormal intestinal lipid absorption IAGP N RGD:5509061 20141003 MGI PMID:11717426 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0005352 small cranium IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0005408 hypopigmentation IAGP N RGD:5509061 20141003 MGI PMID:19202076 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0005621 abnormal cell physiology IEA N RGD:5509061 20111116 MGI 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0008275 failure of endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20141003 MGI PMID:19202076 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0008657 increased interleukin-1 beta secretion IAGP N RGD:5509061 20141003 MGI PMID:19202076 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0008705 increased interleukin-6 secretion IAGP N RGD:5509061 20141003 MGI PMID:19202076 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0009250 abnormal appendicular skeleton morphology IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0009356 decreased liver triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11717426 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19202076 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0009908 protruding tongue IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0010965 decreased compact bone volume IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18025304 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19202076 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0011093 embryonic lethality at implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11431694 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11717426 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19202076 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0013616 decreased volumetric bone mineral density IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0014103 increased chondrocyte apoptosis IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20220609 MGI PMID:29437042 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0020916 increased susceptibility to Herpesvirales infection IEA N RGD:5509061 20200430 MGI 737210 Mbtps1 membrane-bound transcription factor peptidase, site 1 gene MP:0030420 short basicranium IAGP N RGD:5509061 20171214 MGI PMID:18025304 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20151119 MGI PMID:22768253 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:21040809 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0000250 abnormal vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:9623984 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001007 abnormal sympathetic system morphology IAGP N RGD:5509061 20141003 MGI PMID:15652259 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:9861026 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20151119 MGI PMID:22768253 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:10698177 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:14525913 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:9623984 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001353 increased aggression towards mice IAGP N RGD:5509061 20141003 MGI PMID:15314215 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:22084082 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15314215 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20151119 MGI PMID:22768253 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22084082 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:9623984 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20151119 MGI PMID:22768253 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001417 decreased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:15652259 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001431 abnormal eating behavior IAGP N RGD:5509061 20141003 MGI PMID:10698177 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15652259 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:9623984 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:11287097 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:14525913 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:22084082 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001819 abnormal immune cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0001934 increased litter size IAGP N RGD:5509061 20141003 MGI PMID:15314215 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11287097 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11287097 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:14525913 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9623984 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:9861026 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:12859678 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0002452 abnormal professional antigen presenting cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0002494 increased IgM level IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0002495 increased IgA level IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0002722 abnormal immune system organ morphology IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0002862 abnormal righting response IAGP N RGD:5509061 20141003 MGI PMID:11579129 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0003545 increased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:11826154 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0004149 increased bone strength IAGP N RGD:5509061 20141003 MGI PMID:21040809 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:18305161 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0004279 abnormal rostral migratory stream morphology IAGP N RGD:5509061 20141003 MGI PMID:18305161 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20151119 MGI PMID:22768253 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0004890 decreased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:9861026 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0004981 decreased neuronal precursor cell number IAGP N RGD:5509061 20141003 MGI PMID:18305161 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:21040809 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:9623984 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:9861026 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20151119 MGI PMID:22768253 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15652259 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005437 abnormal glycogen level IAGP N RGD:5509061 20141003 MGI PMID:11287097 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:9623984 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20141003 MGI PMID:11287097 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005465 abnormal T-helper 1 physiology IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20151119 MGI PMID:22768253 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15652259 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:22084082 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:14525913 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:9623984 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18305161 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0006387 abnormal T cell number IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008082 increased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008158 increased diameter of femur IAGP N RGD:5509061 20141003 MGI PMID:21040809 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008182 decreased marginal zone B cell number IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008190 decreased transitional stage B cell number IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:21040809 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:22084082 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008501 increased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008554 decreased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008618 decreased circulating interleukin-12 level IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:16330815 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:22084082 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0008907 decreased total fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22084082 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:9861026 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11287097 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0009289 decreased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:22084082 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:14525913 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:9861026 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:21040809 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0009755 impaired behavioral response to alcohol IAGP N RGD:5509061 20141003 MGI PMID:11826154 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:16650144 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:12859678 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:9623984 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20151119 MGI PMID:22768253 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:21040809 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0010182 decreased susceptibility to weight gain IAGP N RGD:5509061 20151119 MGI PMID:22768253 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20151119 MGI PMID:22768253 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20151119 MGI PMID:22768253 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:21040809 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:9623984 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20151119 MGI PMID:22768253 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20141003 MGI PMID:9623984 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0011957 decreased compensatory feeding amount IAGP N RGD:5509061 20151119 MGI PMID:22768253 737212 Npy1r neuropeptide Y receptor Y1 gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:11287097 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0000077 abnormal interparietal bone morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0000088 short mandible IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0000091 short premaxilla IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0000107 abnormal frontal bone morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0000109 abnormal parietal bone morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16488625 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0000536 hydroureter IAGP N RGD:5509061 20141003 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20141003 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15302123 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0001415 increased exploration in new environment IAGP N RGD:5509061 20141003 MGI PMID:15302123 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0001447 abnormal nest building behavior IAGP N RGD:5509061 20141003 MGI PMID:15302123 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:15302123 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0001649 abnormal mandibular symphysis morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0002639 micrognathia IAGP N RGD:5509061 20141003 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0002639 micrognathia IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0002820 abnormal premaxilla morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0003586 dilated ureter IAGP N RGD:5509061 20141003 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0003672 abnormal ureter development IAGP N RGD:5509061 20141003 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0003838 abnormal milk ejection IAGP N RGD:5509061 20141003 MGI PMID:9245518 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0004017 duplex kidney IAGP N RGD:5509061 20141003 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0004220 abnormal peripheral nervous system regeneration IAGP N RGD:5509061 20141003 MGI PMID:12653975 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0004454 absent pterygoid process IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0004476 absent palatine bone IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0004592 small mandible IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0004726 abnormal nasal capsule morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0005076 abnormal cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:16488625 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0006069 abnormal retina neuronal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0006271 abnormal involution of the mammary gland IAGP N RGD:5509061 20141003 MGI PMID:9245518 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0008056 abnormal retina ganglion cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15932596 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0008384 absent nasal capsule IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0008512 disorganized retina inner nuclear layer IAGP N RGD:5509061 20141003 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0009506 abnormal mammary gland alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:9245518 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0009576 oral atresia IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0009888 palatal shelves fail to meet at midline IAGP N RGD:5509061 20230323 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20141003 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0009890 cleft secondary palate IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0009891 abnormal palate bone morphology IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0009905 absent tongue IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:16488625 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0011493 double ureter IAGP N RGD:5509061 20141003 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0011767 ureterocele IAGP N RGD:5509061 20141003 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0012538 persistent hyaloid artery IAGP N RGD:5509061 20141003 MGI PMID:19273906 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0021215 abnormal palatal mesenchymal cell proliferation IAGP N RGD:5509061 20230323 MGI PMID:23863482 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0030012 impaired central nervous system regeneration IAGP N RGD:5509061 20170713 MGI PMID:12653975 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0031330 delayed peripheral nervous system regeneration IAGP N RGD:5509061 20220120 MGI PMID:12653975 737214 Ptprf protein tyrosine phosphatase receptor type F gene MP:0031444 glossoptosis IAGP N RGD:5509061 20230323 MGI PMID:23863482 737215 Camk2g calcium/calmodulin-dependent protein kinase II gamma gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:19741297 737215 Camk2g calcium/calmodulin-dependent protein kinase II gamma gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20171207 MGI PMID:28319059 737215 Camk2g calcium/calmodulin-dependent protein kinase II gamma gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:19741297 737215 Camk2g calcium/calmodulin-dependent protein kinase II gamma gene MP:0008537 increased susceptibility to induced colitis IAGP N RGD:5509061 20171207 MGI PMID:28319059 737215 Camk2g calcium/calmodulin-dependent protein kinase II gamma gene MP:0011081 decreased macrophage apoptosis IAGP N RGD:5509061 20141003 MGI PMID:19741297 737215 Camk2g calcium/calmodulin-dependent protein kinase II gamma gene MP:0013298 increased susceptibility to colitis induced morbidity/mortality IAGP N RGD:5509061 20171207 MGI PMID:28319059 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0000137 abnormal vertebrae morphology IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20231207 MGI 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20210520 MGI 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20210520 MGI 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0000346 broad head IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20210930 MGI PMID:28380258 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0000547 short limbs IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20210930 MGI PMID:28380258 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0000562 polydactyly IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0001178 pulmonary hypoplasia IAGP N RGD:5509061 20210930 MGI PMID:28380258 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0001785 edema IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0001891 hydrocephaly IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20210930 MGI PMID:28380258 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20231207 MGI 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0003109 short femur IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0004134 abnormal chest morphology IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0004600 abnormal vertebral transverse process morphology IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0005104 abnormal tarsal bone morphology IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0005108 abnormal ulna morphology IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0005229 abnormal intervertebral disk development IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0006280 abnormal digit development IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0006393 absent nucleus pulposus IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0008272 abnormal endochondral bone ossification IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0009881 increased mouth size IAGP N RGD:5509061 20230810 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0009907 decreased tongue size IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0010744 abnormal cervical flexure morphology IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0010825 abnormal lung saccule morphology IAGP N RGD:5509061 20210930 MGI PMID:28380258 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0010906 abnormal lung bud morphology IAGP N RGD:5509061 20210930 MGI PMID:28380258 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0010995 abnormal lung alveolus development IAGP N RGD:5509061 20210930 MGI PMID:28380258 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0011024 abnormal branching involved in lung morphogenesis IAGP N RGD:5509061 20210930 MGI PMID:28380258 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20210930 MGI PMID:28380258 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0011142 abnormal lung-associated mesenchyme development IAGP N RGD:5509061 20210930 MGI PMID:28380258 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0011143 thick lung-associated mesenchyme IAGP N RGD:5509061 20210930 MGI PMID:28380258 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0011148 decreased mesenchymal cell proliferation involved in lung development IAGP N RGD:5509061 20210930 MGI PMID:28380258 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0012676 dilated brain ventricle IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0012719 abnormal neck morphology IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0012721 short neck IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20151112 MGI PMID:24853502 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0013203 abnormal primary cilium morphology IAGP N RGD:5509061 20210930 MGI PMID:28380258 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0014105 abnormal chondrocyte differentiation IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0020137 decreased bone mineralization IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0030190 small snout IAGP N RGD:5509061 20210930 MGI PMID:29098359 737218 Cilk1 ciliogenesis associated kinase 1 gene MP:0030941 enhanced autophagy IAGP N RGD:5509061 20210930 MGI PMID:28380258 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20170105 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20170105 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20181227 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20210128 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15890676 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:15890676 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15890676 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:15890676 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0002834 decreased heart weight IEA N RGD:5509061 20181227 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20170105 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20170105 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20170105 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20141003 MGI PMID:15890676 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201231 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20170105 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20170105 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20170105 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20210128 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:15890676 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0008995 early reproductive senescence IAGP N RGD:5509061 20141003 MGI PMID:15890676 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0009198 abnormal male genitalia morphology IEA N RGD:5509061 20210826 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0009204 absent external male genitalia IEA N RGD:5509061 20220519 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20170105 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20170105 MGI 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15169901 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0011385 abnormal testosterone level IAGP N RGD:5509061 20141003 MGI PMID:15890676 737222 Cyp17a1 cytochrome P450, family 17, subfamily a, polypeptide 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20170105 MGI 737227 Tnfrsf8 tumor necrosis factor receptor superfamily, member 8 gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:8598042 737227 Tnfrsf8 tumor necrosis factor receptor superfamily, member 8 gene MP:0000714 increased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:8598042 737227 Tnfrsf8 tumor necrosis factor receptor superfamily, member 8 gene MP:0005673 decreased susceptibility to graft versus host disease IAGP N RGD:5509061 20141003 MGI PMID:15322151 737228 Tnr tenascin R gene MP:0001565 abnormal circulating phosphate level IEA N RGD:5509061 20211021 MGI 737228 Tnr tenascin R gene MP:0003313 abnormal locomotor activation IEA N RGD:5509061 20220811 MGI 737228 Tnr tenascin R gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:10341229 737228 Tnr tenascin R gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:12532406 737228 Tnr tenascin R gene MP:0004952 increased spleen weight IEA N RGD:5509061 20211021 MGI 737228 Tnr tenascin R gene MP:0008263 abnormal hippocampus CA1 region morphology IAGP N RGD:5509061 20141003 MGI PMID:12532406 737228 Tnr tenascin R gene MP:0008284 abnormal hippocampus pyramidal cell layer IAGP N RGD:5509061 20141003 MGI PMID:12532406 737228 Tnr tenascin R gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20141003 MGI PMID:10341229 737228 Tnr tenascin R gene MP:0009538 abnormal synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:12532406 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20210128 MGI 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20200310 MGI PMID:9843206 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0001147 small testis IAGP N RGD:5509061 20200310 MGI PMID:9843206 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20200310 MGI PMID:11564714 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20200310 MGI PMID:9843206 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:11564714 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20200310 MGI PMID:9843206 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:9843206 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:11564714 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:9843206 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20200310 MGI PMID:11564714 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0002160 abnormal reproductive system morphology IEA N RGD:5509061 20200402 MGI 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20200310 MGI PMID:15944188 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20200310 MGI PMID:11564714 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0002995 primary sex reversal IAGP N RGD:5509061 20200310 MGI PMID:15944188 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0002996 ovotestis IAGP N RGD:5509061 20200310 MGI PMID:15944188 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20200310 MGI PMID:12538527 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0004728 abnormal efferent ductules of testis morphology IAGP N RGD:5509061 20200310 MGI PMID:11564714 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0004806 absent germ cells IAGP N RGD:5509061 20200310 MGI PMID:9843206 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:11564714 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20200310 MGI PMID:9843206 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20200310 MGI PMID:9843206 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0005564 increased hemoglobin content IEA N RGD:5509061 20210128 MGI 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0006262 increased testis tumor incidence IAGP N RGD:5509061 20200310 MGI PMID:11564714 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0006417 rete testis obstruction IAGP N RGD:5509061 20200310 MGI PMID:11564714 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0006418 abnormal testis cord formation IAGP N RGD:5509061 20200310 MGI PMID:12538527 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0006419 disorganized testis cords IAGP N RGD:5509061 20200310 MGI PMID:12538527 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0006420 abnormal peritubular myoid cell morphology IAGP N RGD:5509061 20200310 MGI PMID:11564714 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0006421 decreased number of peritubular myoid cells IAGP N RGD:5509061 20200310 MGI PMID:12538527 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0006427 ectopic Leydig cells IAGP N RGD:5509061 20200310 MGI PMID:11564714 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0006427 ectopic Leydig cells IAGP N RGD:5509061 20200310 MGI PMID:12538527 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0006428 ectopic Sertoli cells IAGP N RGD:5509061 20200310 MGI PMID:11564714 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0008297 retention of the adrenal gland x-zone IAGP N RGD:5509061 20200310 MGI PMID:9843206 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20211021 MGI 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0009257 dilated seminiferous tubule IAGP N RGD:5509061 20200310 MGI PMID:11564714 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0009433 polyovular ovarian follicle IAGP N RGD:5509061 20200310 MGI PMID:9843206 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20211021 MGI 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:11564714 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20200310 MGI PMID:9843206 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0013603 abnormal fetal Leydig cell differentiation IAGP N RGD:5509061 20200310 MGI PMID:12538527 737230 Nr0b1 nuclear receptor subfamily 0, group B, member 1 gene MP:0031407 increased Sertoli cell proliferation IAGP N RGD:5509061 20220630 MGI PMID:11564714 737233 Ddx1 DEAD box helicase 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737233 Ddx1 DEAD box helicase 1 gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 737233 Ddx1 DEAD box helicase 1 gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:21983831 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:21983831 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21983831 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:21983831 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21983831 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21983831 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:21983831 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:21983831 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:21983831 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:21983831 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:21983831 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:21983831 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0008682 decreased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:21983831 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0008688 decreased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:21983831 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:21983831 737235 Map4k3 mitogen-activated protein kinase kinase kinase kinase 3 gene MP:0010221 abnormal T-helper 17 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21983831 737238 Adcy2 adenylate cyclase 2 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 737241 Mapk13 mitogen-activated protein kinase 13 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19135240 737241 Mapk13 mitogen-activated protein kinase 13 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15729360 737241 Mapk13 mitogen-activated protein kinase 13 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:19135240 737241 Mapk13 mitogen-activated protein kinase 13 gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:19135240 737241 Mapk13 mitogen-activated protein kinase 13 gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19135240 737241 Mapk13 mitogen-activated protein kinase 13 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19135240 737241 Mapk13 mitogen-activated protein kinase 13 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20201022 MGI 737241 Mapk13 mitogen-activated protein kinase 13 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19135240 737241 Mapk13 mitogen-activated protein kinase 13 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19135240 737244 Akap12 A kinase anchor protein 12 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:24058627 737244 Akap12 A kinase anchor protein 12 gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0001158 abnormal prostate gland morphology IAGP N RGD:5509061 20141003 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0001175 abnormal lung morphology IAGP N RGD:5509061 20141003 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0001924 infertility IAGP N RGD:5509061 20141003 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:11429284 737244 Akap12 A kinase anchor protein 12 gene MP:0002683 delayed fertility IAGP N RGD:5509061 20141003 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20220303 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:24058627 737244 Akap12 A kinase anchor protein 12 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:24058627 737244 Akap12 A kinase anchor protein 12 gene MP:0004961 increased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0005305 prostate gland anterior lobe hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20141003 MGI PMID:24058627 737244 Akap12 A kinase anchor protein 12 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0008975 delayed male fertility IAGP N RGD:5509061 20141003 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0008976 delayed female fertility IAGP N RGD:5509061 20141003 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:24058627 737244 Akap12 A kinase anchor protein 12 gene MP:0031365 prostate gland ventral lobe hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:18593908 737244 Akap12 A kinase anchor protein 12 gene MP:0031635 increased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:24058627 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0000428 abnormal craniofacial morphology IEA N RGD:5509061 20190502 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0000438 abnormal cranium morphology IEA N RGD:5509061 20190502 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20190502 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0000841 abnormal hindbrain morphology IEA N RGD:5509061 20190502 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0000914 exencephaly IEA N RGD:5509061 20210520 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0001293 anophthalmia IEA N RGD:5509061 20210520 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20230601 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0001672 abnormal embryo development IEA N RGD:5509061 20210520 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20190502 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0001785 edema IEA N RGD:5509061 20230601 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0002102 abnormal ear morphology IEA N RGD:5509061 20190502 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0002109 abnormal limb morphology IEA N RGD:5509061 20190502 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0002111 abnormal tail morphology IEA N RGD:5509061 20230601 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20240523 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0003717 pallor IEA N RGD:5509061 20190502 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0003720 abnormal neural tube closure IEA N RGD:5509061 20190502 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20190502 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20210520 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0008797 facial cleft IEA N RGD:5509061 20210520 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0009908 protruding tongue IEA N RGD:5509061 20210520 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0011495 abnormal head shape IEA N RGD:5509061 20190502 MGI 737245 Slc25a1 solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 gene MP:0011496 abnormal head size IEA N RGD:5509061 20190502 MGI 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0001270 distended abdomen IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0001326 retina degeneration IAGP N RGD:5509061 20200206 MGI PMID:26814127 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0002928 abnormal bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0002929 abnormal bile duct development IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0003254 bile duct inflammation IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0003336 pancreas cyst IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0003675 kidney cyst IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0004021 abnormal rod electrophysiology IAGP N RGD:5509061 20200206 MGI PMID:26814127 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20200206 MGI PMID:26814127 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0004247 small pancreas IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0008444 retina cone cell degeneration IAGP N RGD:5509061 20200206 MGI PMID:26814127 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0008451 retina rod cell degeneration IAGP N RGD:5509061 20200206 MGI PMID:26814127 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0008456 abnormal retina rod cell outer segment morphology IAGP N RGD:5509061 20200206 MGI PMID:26814127 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0008511 thin retina inner nuclear layer IAGP N RGD:5509061 20200206 MGI PMID:26814127 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0008518 retina outer nuclear layer degeneration IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0008585 absent photoreceptor outer segment IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0008587 short photoreceptor outer segment IAGP N RGD:5509061 20200206 MGI PMID:26814127 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0009343 dilated gallbladder IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0009498 abnormal extrahepatic bile duct morphology IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0009619 abnormal optokinetic reflex IAGP N RGD:5509061 20200206 MGI PMID:26814127 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20200206 MGI PMID:26814127 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16565502 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0011965 decreased total retina thickness IAGP N RGD:5509061 20200206 MGI PMID:26814127 737247 Arl3 ADP-ribosylation factor-like 3 gene MP:0014059 abnormal photoreceptor connecting cilium morphology IAGP N RGD:5509061 20200206 MGI PMID:26814127 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:16195467 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16195467 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:16195467 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16195467 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16195467 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16195467 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0002694 abnormal pancreas secretion IAGP N RGD:5509061 20141003 MGI PMID:16195467 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0002791 steatorrhea IAGP N RGD:5509061 20141003 MGI PMID:16195467 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0003867 increased defecation amount IAGP N RGD:5509061 20141003 MGI PMID:16195467 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:16195467 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0005310 abnormal salivary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:16195467 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:16195467 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16195467 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:16195467 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0009161 pancreatic acinar cell zymogen granule accumulation IAGP N RGD:5509061 20141003 MGI PMID:16195467 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0013368 abnormal sweat gland physiology IAGP N RGD:5509061 20150430 MGI PMID:25329695 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0013371 hypohidrosis IAGP N RGD:5509061 20150430 MGI PMID:25329695 737250 Itpr2 inositol 1,4,5-triphosphate receptor 2 gene MP:0014476 abnormal feces lipid level IAGP N RGD:5509061 20240704 MGI PMID:16195467 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:21333348 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:21333348 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19103808 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19726872 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:15042706 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:21333348 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:21333348 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0004889 increased energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0004909 increased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:21333348 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0004928 increased epididymis weight IAGP N RGD:5509061 20141003 MGI PMID:21333348 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:19103808 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19103808 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19726872 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0005628 decreased circulating potassium level IEA N RGD:5509061 20181227 MGI 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0008280 abnormal male germ cell apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21333348 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20170803 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20220811 MGI 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0009167 increased pancreatic islet number IAGP N RGD:5509061 20170803 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0009283 decreased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20150611 MGI PMID:19726872 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20170803 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0014342 abnormal muscle fiber mitochondrial morphology IAGP N RGD:5509061 20240118 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0030016 increased adipocyte glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0030021 increased muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:17693256 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0030603 increased sperm number IAGP N RGD:5509061 20180621 MGI PMID:21333348 737251 Ptprv protein tyrosine phosphatase receptor type V gene MP:0030969 increased circulating adiponectin level IAGP N RGD:5509061 20190815 MGI PMID:17693256 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0000005 increased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0000008 increased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:19624751 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20201022 MGI 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0000274 enlarged heart IEA N RGD:5509061 20201022 MGI 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:17943087 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:19910458 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17943087 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:19910458 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:19624751 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20211021 MGI 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001399 hyperactivity IEA N RGD:5509061 20230601 MGI 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:19624751 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:17943087 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:19910458 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:17943087 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:19910458 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20210520 MGI 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:19624751 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0002135 abnormal kidney morphology IEA N RGD:5509061 20210826 MGI 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:17943087 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17943087 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:17943087 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:19910458 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:19624751 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0002989 small kidney IEA N RGD:5509061 20210826 MGI 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20220811 MGI 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:19910458 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0004924 abnormal behavior IEA N RGD:5509061 20230601 MGI 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:19624751 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0005290 decreased oxygen consumption IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:19624751 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:19624751 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0005458 increased percent body fat/body weight IAGP N RGD:5509061 20160407 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19624751 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0005658 increased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:19624751 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:19624751 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0006203 eye hemorrhage IEA N RGD:5509061 20210128 MGI 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:17943087 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:19910458 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0009121 increased white fat cell lipid droplet size IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20200514 MGI 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20220324 MGI PMID:17943087 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0009288 increased epididymal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19624751 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0009304 increased retroperitoneal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:19624751 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0010378 increased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:19624751 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20141003 MGI PMID:19624751 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0011698 abnormal brown adipose tissue physiology IAGP N RGD:5509061 20141003 MGI PMID:19194461 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:19910458 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0020870 decreased thigmotaxis IEA N RGD:5509061 20230601 MGI 737255 Kdm3a lysine (K)-specific demethylase 3A gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220324 MGI PMID:17943087 737256 Sst somatostatin gene MP:0001399 hyperactivity IAGP N RGD:5509061 20160929 MGI PMID:27007844 737256 Sst somatostatin gene MP:0001409 increased stereotypic behavior IAGP N RGD:5509061 20160304 MGI PMID:26590342 737256 Sst somatostatin gene MP:0001745 increased circulating corticosterone level IAGP N RGD:5509061 20141003 MGI PMID:11430867 737256 Sst somatostatin gene MP:0002064 seizures IAGP N RGD:5509061 20160304 MGI PMID:26590342 737256 Sst somatostatin gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21971153 737256 Sst somatostatin gene MP:0002083 premature death IAGP N RGD:5509061 20160304 MGI PMID:26590342 737256 Sst somatostatin gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 737256 Sst somatostatin gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:16706848 737256 Sst somatostatin gene MP:0002804 abnormal motor learning IAGP N RGD:5509061 20141003 MGI PMID:11430867 737256 Sst somatostatin gene MP:0002911 abnormal inhibitory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:16706848 737256 Sst somatostatin gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:16706848 737256 Sst somatostatin gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20161201 MGI 737256 Sst somatostatin gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20161201 MGI 737256 Sst somatostatin gene MP:0003212 increased susceptibility to age related obesity IAGP N RGD:5509061 20141003 MGI PMID:11413165 737256 Sst somatostatin gene MP:0003883 enlarged stomach IAGP N RGD:5509061 20141003 MGI PMID:15735748 737256 Sst somatostatin gene MP:0003892 abnormal gastric gland morphology IAGP N RGD:5509061 20141003 MGI PMID:15735748 737256 Sst somatostatin gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20201022 MGI 737256 Sst somatostatin gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20160304 MGI PMID:26590342 737256 Sst somatostatin gene MP:0004139 abnormal gastric parietal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:15735748 737256 Sst somatostatin gene MP:0004731 increased circulating gastrin level IAGP N RGD:5509061 20141003 MGI PMID:14555768 737256 Sst somatostatin gene MP:0005116 abnormal circulating pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:11413165 737256 Sst somatostatin gene MP:0005121 decreased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:21971153 737256 Sst somatostatin gene MP:0005123 increased circulating growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:11430867 737256 Sst somatostatin gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:11413165 737256 Sst somatostatin gene MP:0008002 hyperchlorhydria IAGP N RGD:5509061 20141003 MGI PMID:15735748 737256 Sst somatostatin gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20201022 MGI 737256 Sst somatostatin gene MP:0009436 fragmentation of sleep/wake states IAGP N RGD:5509061 20220922 MGI PMID:27007844 737256 Sst somatostatin gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20210429 MGI PMID:33029009 737256 Sst somatostatin gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20201022 MGI 737256 Sst somatostatin gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20161201 MGI 737256 Sst somatostatin gene MP:0010778 abnormal stomach fundus morphology IAGP N RGD:5509061 20141003 MGI PMID:15735748 737256 Sst somatostatin gene MP:0011612 increased circulating ghrelin level IAGP N RGD:5509061 20141003 MGI PMID:21971153 737256 Sst somatostatin gene MP:0014114 abnormal cognition IAGP N RGD:5509061 20160929 MGI PMID:27007844 737260 St8sia1 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20200310 MGI PMID:11133999 737260 St8sia1 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20200310 MGI PMID:11133999 737260 St8sia1 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20200310 MGI PMID:11133999 737260 St8sia1 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20200310 MGI PMID:11133999 737260 St8sia1 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 gene MP:0002064 seizures IAGP N RGD:5509061 20200310 MGI PMID:11133999 737260 St8sia1 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20200310 MGI PMID:11133999 737260 St8sia1 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:11133999 737260 St8sia1 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 gene MP:0003997 tonic-clonic seizures IAGP N RGD:5509061 20200310 MGI PMID:11133999 737260 St8sia1 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 gene MP:0004858 abnormal nervous system regeneration IAGP N RGD:5509061 20200310 MGI PMID:11682464 737260 St8sia1 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20200310 MGI PMID:11682464 737260 St8sia1 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20200310 MGI PMID:11682464 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:20375365 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0000272 abnormal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:20375365 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:20375365 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:23999430 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0001863 blood vessel inflammation IAGP N RGD:5509061 20141003 MGI PMID:23999430 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20375365 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20141003 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:17438289 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0002844 aortic hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:20375365 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0002893 ketoaciduria IAGP N RGD:5509061 20141003 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0003383 abnormal gluconeogenesis IAGP N RGD:5509061 20141003 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0003441 increased glycerol level IAGP N RGD:5509061 20141003 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0003814 vascular smooth muscle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23999430 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:17438289 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:20375365 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:17438289 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:17438289 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:23999430 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0005266 abnormal metabolism IAGP N RGD:5509061 20141003 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0005292 improved glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0005311 abnormal circulating amino acid level IAGP N RGD:5509061 20141003 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0005330 cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:20375365 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0005339 increased susceptibility to atherosclerosis IAGP N RGD:5509061 20141003 MGI PMID:23999430 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:23999430 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17438289 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23999430 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0009871 abnormal aorta tunica adventitia morphology IAGP N RGD:5509061 20141003 MGI PMID:20375365 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0009873 abnormal aorta tunica media morphology IAGP N RGD:5509061 20141003 MGI PMID:20375365 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0010080 abnormal hepatocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0010574 dilated aorta IAGP N RGD:5509061 20141003 MGI PMID:20375365 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0010658 thoracic aorta aneurysm IAGP N RGD:5509061 20141003 MGI PMID:20375365 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0010659 abdominal aorta aneurysm IAGP N RGD:5509061 20141003 MGI PMID:20375365 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0013404 decreased circulating lactate level IAGP N RGD:5509061 20141225 MGI PMID:17403374 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0031274 increased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:20375365 737262 Klf15 Kruppel-like transcription factor 15 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:17438289 737264 Hnrnpl heterogeneous nuclear ribonucleoprotein L gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:22523384 737264 Hnrnpl heterogeneous nuclear ribonucleoprotein L gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:22523384 737264 Hnrnpl heterogeneous nuclear ribonucleoprotein L gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22523384 737264 Hnrnpl heterogeneous nuclear ribonucleoprotein L gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:22523384 737264 Hnrnpl heterogeneous nuclear ribonucleoprotein L gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:22523384 737264 Hnrnpl heterogeneous nuclear ribonucleoprotein L gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:22523384 737264 Hnrnpl heterogeneous nuclear ribonucleoprotein L gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22523384 737264 Hnrnpl heterogeneous nuclear ribonucleoprotein L gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22523384 737264 Hnrnpl heterogeneous nuclear ribonucleoprotein L gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22523384 737265 Cyp4f14 cytochrome P450, family 4, subfamily f, polypeptide 14 gene MP:0001289 persistence of hyaloid vascular system IEA N RGD:5509061 20240523 MGI 737265 Cyp4f14 cytochrome P450, family 4, subfamily f, polypeptide 14 gene MP:0001303 abnormal lens morphology IEA N RGD:5509061 20181227 MGI 737265 Cyp4f14 cytochrome P450, family 4, subfamily f, polypeptide 14 gene MP:0001304 cataract IEA N RGD:5509061 20181227 MGI 737265 Cyp4f14 cytochrome P450, family 4, subfamily f, polypeptide 14 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20220811 MGI 737265 Cyp4f14 cytochrome P450, family 4, subfamily f, polypeptide 14 gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20220811 MGI 737265 Cyp4f14 cytochrome P450, family 4, subfamily f, polypeptide 14 gene MP:0003868 abnormal feces composition IAGP N RGD:5509061 20141003 MGI PMID:22665481 737265 Cyp4f14 cytochrome P450, family 4, subfamily f, polypeptide 14 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:22665481 737265 Cyp4f14 cytochrome P450, family 4, subfamily f, polypeptide 14 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:22665481 737265 Cyp4f14 cytochrome P450, family 4, subfamily f, polypeptide 14 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22665481 737265 Cyp4f14 cytochrome P450, family 4, subfamily f, polypeptide 14 gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20220811 MGI 737268 Dap death-associated protein gene MP:0001312 abnormal cornea morphology IEA N RGD:5509061 20201231 MGI 737268 Dap death-associated protein gene MP:0001554 increased circulating free fatty acids level IEA N RGD:5509061 20160114 MGI 737268 Dap death-associated protein gene MP:0002833 increased heart weight IEA N RGD:5509061 20201022 MGI 737268 Dap death-associated protein gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20220811 MGI 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:16430881 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:15143159 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15308581 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15863464 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:19028670 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000274 enlarged heart IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11593045 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:11984589 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12072561 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15109497 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15485910 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15601645 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15652482 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15863464 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:16374517 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:19028670 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22619176 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:11593045 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:12072561 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15485910 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:15863464 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:18297725 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:19028670 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0000343 abnormal response to cardiac infarction IAGP N RGD:5509061 20141003 MGI PMID:21270129 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001284 absent vibrissae IEA N RGD:5509061 20230601 MGI 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:11593045 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17450150 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:12072561 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15109497 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15132980 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15652482 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15863464 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:16374517 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19028670 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19683723 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:21947295 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:22082674 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:15485910 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001855 abnormal atrial thrombosis IAGP N RGD:5509061 20141003 MGI PMID:15601645 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:11593045 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11179202 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11593045 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12072561 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15308581 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15601645 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15652482 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15863464 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:19028670 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22426213 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002083 premature death IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16106363 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:9550726 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002190 disorganized myocardium IAGP N RGD:5509061 20141003 MGI PMID:16374517 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002192 hydrops fetalis IAGP N RGD:5509061 20141003 MGI PMID:15109497 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20181227 MGI 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:11689889 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002740 heart hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18297725 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15863464 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:16374517 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:17450150 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:15863464 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:11984589 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:12072561 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:14963485 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15109497 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15601645 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15652482 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:15863464 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:19028670 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:19797173 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:22426213 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:11593045 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19028670 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:19683723 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:22082674 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:22426213 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002837 dystrophic cardiac calcinosis IAGP N RGD:5509061 20141003 MGI PMID:22426213 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002952 ventricular cardiomyopathy IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:21947295 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15652482 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19683723 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0002972 abnormal cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19797173 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003022 increased coronary flow rate IAGP N RGD:5509061 20201119 MGI PMID:18312674 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:18312674 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003038 decreased myocardial infarct size IAGP N RGD:5509061 20141003 MGI PMID:21270129 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:15863464 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003137 abnormal impulse conducting system conduction IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:15485910 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15652482 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17663739 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:19797173 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22082674 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22426213 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003222 increased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22082674 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003223 decreased cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:21270129 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:12072561 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003233 prolonged QT interval IAGP N RGD:5509061 20141003 MGI PMID:15863464 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:11593045 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003828 pulmonary edema IAGP N RGD:5509061 20141003 MGI PMID:22082674 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:15132980 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:21947295 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003920 abnormal heart right ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19028670 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:15132980 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19028670 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15143159 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004032 abnormal interventricular groove morphology IAGP N RGD:5509061 20141003 MGI PMID:15143159 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004039 abnormal cardiac muscle cell glucose uptake IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004057 thin myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:15143159 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004076 abnormal vitelline vascular remodeling IAGP N RGD:5509061 20141003 MGI PMID:16946137 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:11984589 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:15132980 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:22426213 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004117 abnormal atrioventricular bundle morphology IAGP N RGD:5509061 20141003 MGI PMID:15109497 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004123 abnormal impulse conducting system morphology IAGP N RGD:5509061 20141003 MGI PMID:15109497 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:15132980 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:15308581 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:16946137 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:19683723 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:22426213 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:22619176 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:19683723 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:22082674 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:22426213 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:22619176 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004486 decreased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:11689889 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:11593045 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:15601645 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:21947295 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:22082674 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004564 increased myocardial fiber size IAGP N RGD:5509061 20141003 MGI PMID:22426213 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004566 myocardial fiber degeneration IAGP N RGD:5509061 20141003 MGI PMID:19797173 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004567 decreased myocardial fiber number IAGP N RGD:5509061 20141003 MGI PMID:15863464 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21947295 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15132980 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15308581 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15601645 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22082674 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:11984589 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:19028670 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:21947295 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:16374517 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15652482 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16946137 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:23372168 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005522 increased circulating atrial natriuretic factor IAGP N RGD:5509061 20141003 MGI PMID:21947295 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11984589 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:12072561 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:14963485 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19683723 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22426213 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22619176 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:11593045 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:14963485 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:15109497 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0005608 cardiac interstitial fibrosis IAGP N RGD:5509061 20141003 MGI PMID:16374517 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:22619176 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:15485910 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:17450150 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:22082674 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:22426213 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:21947295 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:15863464 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0006267 abnormal intercalated disk morphology IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20141003 MGI PMID:22426213 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0008022 dilated heart ventricle IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:14963485 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:15308581 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0008260 abnormal autophagy IAGP N RGD:5509061 20141003 MGI PMID:22619176 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:11593045 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20231221 MGI PMID:12072561 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0008842 lipofuscinosis IAGP N RGD:5509061 20141003 MGI PMID:22619176 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15132980 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:17450150 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19683723 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:15863464 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0009548 abnormal platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:23372168 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11984589 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17450150 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19683723 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010018 pulmonary vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15601645 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010019 liver vascular congestion IAGP N RGD:5509061 20141003 MGI PMID:15485910 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210520 MGI 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010334 pleural effusion IAGP N RGD:5509061 20141003 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20141003 MGI PMID:15863464 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010392 prolonged QRS complex duration IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010432 common ventricle IAGP N RGD:5509061 20141003 MGI PMID:15143159 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:15109497 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010519 atrioventricular block IAGP N RGD:5509061 20141003 MGI PMID:19028670 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010533 atrioventricular node hypoplasia IAGP N RGD:5509061 20231221 MGI PMID:15109497 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010546 abnormal subendocardium layer morphology IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:15132980 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010551 abnormal coronary vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:21270129 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010559 heart block IAGP N RGD:5509061 20141003 MGI PMID:17785437 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:22426213 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010636 bundle branch block IAGP N RGD:5509061 20150910 MGI PMID:24108106 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:15132980 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010724 thick interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:21947295 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:19028670 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010725 thin interventricular septum IAGP N RGD:5509061 20141003 MGI PMID:22426213 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:15132980 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010754 abnormal heart left ventricle pressure IAGP N RGD:5509061 20141003 MGI PMID:18312674 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:22619176 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12072561 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15485910 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11689889 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15109497 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:14657344 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16946137 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15143159 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0011392 increased fetal cardiomyocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22619176 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231109 MGI PMID:11984589 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0014316 decreased heart left ventricle posterior wall thickness IAGP N RGD:5509061 20231221 MGI PMID:15652482 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0014317 decreased heart left ventricle septal wall thickness IAGP N RGD:5509061 20231109 MGI PMID:11984589 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0014519 myocardial ventricular hypertrabeculation IAGP N RGD:5509061 20240822 MGI PMID:15109497 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0021155 abnormal heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:19797173 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0021157 increased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:15132980 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0031511 globular heart IAGP N RGD:5509061 20231102 MGI PMID:15485910 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:11884376 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:12072561 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:14963485 737271 Myl2 myosin, light polypeptide 2, regulatory, cardiac, slow gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:15863464 737273 Tesk2 testis-specific kinase 2 gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20240523 MGI 737273 Tesk2 testis-specific kinase 2 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 737273 Tesk2 testis-specific kinase 2 gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20210128 MGI 737275 Crtac1 cartilage acidic protein 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20210520 MGI 737275 Crtac1 cartilage acidic protein 1 gene MP:0005237 abnormal olfactory tract morphology IAGP N RGD:5509061 20141003 MGI PMID:21817055 737275 Crtac1 cartilage acidic protein 1 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:21817055 737275 Crtac1 cartilage acidic protein 1 gene MP:0010052 increased grip strength IEA N RGD:5509061 20211021 MGI 737278 Slc22a1 solute carrier family 22 (organic cation transporter), member 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:11463829 737278 Slc22a1 solute carrier family 22 (organic cation transporter), member 1 gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:11463829 737278 Slc22a1 solute carrier family 22 (organic cation transporter), member 1 gene MP:0002139 abnormal hepatobiliary system physiology IAGP N RGD:5509061 20141003 MGI PMID:11463829 737278 Slc22a1 solute carrier family 22 (organic cation transporter), member 1 gene MP:0006273 abnormal urine organic cation level IAGP N RGD:5509061 20141003 MGI PMID:11463829 737278 Slc22a1 solute carrier family 22 (organic cation transporter), member 1 gene MP:0006273 abnormal urine organic cation level IAGP N RGD:5509061 20141003 MGI PMID:14560032 737278 Slc22a1 solute carrier family 22 (organic cation transporter), member 1 gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20160915 MGI PMID:17476361 737278 Slc22a1 solute carrier family 22 (organic cation transporter), member 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20141003 MGI PMID:11463829 737278 Slc22a1 solute carrier family 22 (organic cation transporter), member 1 gene MP:0008875 abnormal xenobiotic pharmacokinetics IAGP N RGD:5509061 20160915 MGI PMID:17476361 737278 Slc22a1 solute carrier family 22 (organic cation transporter), member 1 gene MP:0013277 abnormal fasting circulating glucose level IAGP N RGD:5509061 20160915 MGI PMID:17476361 737278 Slc22a1 solute carrier family 22 (organic cation transporter), member 1 gene MP:0020101 abnormal hepatic glucose production IAGP N RGD:5509061 20160915 MGI PMID:17476361 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0000226 abnormal mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:12133842 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:17475664 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17475664 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12133842 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:11792714 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0001762 polyuria IAGP N RGD:5509061 20141003 MGI PMID:21849488 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0002593 high mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12133842 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:12133842 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:11792714 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:21849488 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0003378 early sexual maturation IAGP N RGD:5509061 20141003 MGI PMID:17475664 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0003830 abnormal testis development IAGP N RGD:5509061 20141003 MGI PMID:17475664 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0004109 abnormal Sertoli cell development IAGP N RGD:5509061 20141003 MGI PMID:17475664 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17475664 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20141003 MGI PMID:17475664 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:17475664 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0005556 abnormal renal filtration rate IAGP N RGD:5509061 20141003 MGI PMID:21849488 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:21849488 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11792714 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17475664 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11792714 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12133842 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0011467 decreased urine urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:21849488 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0011471 decreased urine creatinine level IAGP N RGD:5509061 20141003 MGI PMID:21849488 737280 Slc14a1 solute carrier family 14 (urea transporter), member 1 gene MP:0011941 increased fluid intake IAGP N RGD:5509061 20141003 MGI PMID:21849488 737286 Mpdz multiple PDZ domain crumbs cell polarity complex component gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20201022 MGI 737286 Mpdz multiple PDZ domain crumbs cell polarity complex component gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20181227 MGI 737286 Mpdz multiple PDZ domain crumbs cell polarity complex component gene MP:0002570 alcohol aversion IAGP N RGD:5509061 20151217 MGI PMID:24118405 737286 Mpdz multiple PDZ domain crumbs cell polarity complex component gene MP:0002792 abnormal retina vasculature morphology IEA N RGD:5509061 20181227 MGI 737286 Mpdz multiple PDZ domain crumbs cell polarity complex component gene MP:0002833 increased heart weight IEA N RGD:5509061 20181227 MGI 737286 Mpdz multiple PDZ domain crumbs cell polarity complex component gene MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20151217 MGI PMID:24118405 737286 Mpdz multiple PDZ domain crumbs cell polarity complex component gene MP:0004738 abnormal auditory brainstem response IEA N RGD:5509061 20201022 MGI 737286 Mpdz multiple PDZ domain crumbs cell polarity complex component gene MP:0005292 improved glucose tolerance IEA N RGD:5509061 20211021 MGI 737286 Mpdz multiple PDZ domain crumbs cell polarity complex component gene MP:0005627 increased circulating potassium level IEA N RGD:5509061 20230601 MGI 737286 Mpdz multiple PDZ domain crumbs cell polarity complex component gene MP:0009775 increased behavioral withdrawal response IAGP N RGD:5509061 20151217 MGI PMID:24118405 737286 Mpdz multiple PDZ domain crumbs cell polarity complex component gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 737286 Mpdz multiple PDZ domain crumbs cell polarity complex component gene MP:0010097 abnormal retina blood vessel morphology IEA N RGD:5509061 20181227 MGI 737287 Cacng1 calcium channel, voltage-dependent, gamma subunit 1 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:10799530 737287 Cacng1 calcium channel, voltage-dependent, gamma subunit 1 gene MP:0004145 abnormal muscle electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11495636 737290 Bdh1 3-hydroxybutyrate dehydrogenase, type 1 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20190530 MGI PMID:30668551 737290 Bdh1 3-hydroxybutyrate dehydrogenase, type 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20190530 MGI PMID:30668551 737290 Bdh1 3-hydroxybutyrate dehydrogenase, type 1 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:30668551 737294 Npm2 nucleophosmin/nucleoplasmin 2 gene MP:0001125 abnormal oocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:12714744 737294 Npm2 nucleophosmin/nucleoplasmin 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:12714744 737294 Npm2 nucleophosmin/nucleoplasmin 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:12714744 737294 Npm2 nucleophosmin/nucleoplasmin 2 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12714744 737295 Rasa3 RAS p21 protein activator 3 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20191212 MGI PMID:25705885 737295 Rasa3 RAS p21 protein activator 3 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20191212 MGI PMID:29922180 737295 Rasa3 RAS p21 protein activator 3 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0000603 pale liver IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0000685 abnormal immune system morphology IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20191212 MGI PMID:25705885 737295 Rasa3 RAS p21 protein activator 3 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 737295 Rasa3 RAS p21 protein activator 3 gene MP:0001548 hyperlipidemia IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0001577 anemia IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0001634 internal hemorrhage IAGP N RGD:5509061 20150416 MGI PMID:2383655 737295 Rasa3 RAS p21 protein activator 3 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17179160 737295 Rasa3 RAS p21 protein activator 3 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:17179160 737295 Rasa3 RAS p21 protein activator 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17179160 737295 Rasa3 RAS p21 protein activator 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0002083 premature death IAGP N RGD:5509061 20150416 MGI PMID:2383655 737295 Rasa3 RAS p21 protein activator 3 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20191212 MGI PMID:25705885 737295 Rasa3 RAS p21 protein activator 3 gene MP:0002599 increased mean platelet volume IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 737295 Rasa3 RAS p21 protein activator 3 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20191212 MGI PMID:25705885 737295 Rasa3 RAS p21 protein activator 3 gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0003396 abnormal embryonic hematopoiesis IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0003542 abnormal vascular endothelial cell development IAGP N RGD:5509061 20141003 MGI PMID:17179160 737295 Rasa3 RAS p21 protein activator 3 gene MP:0003674 oxidative stress IAGP N RGD:5509061 20191212 MGI PMID:29922180 737295 Rasa3 RAS p21 protein activator 3 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0003717 pallor IAGP N RGD:5509061 20150416 MGI PMID:2383655 737295 Rasa3 RAS p21 protein activator 3 gene MP:0003717 pallor IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0003718 maternal effect IAGP N RGD:5509061 20191219 MGI PMID:8334700 737295 Rasa3 RAS p21 protein activator 3 gene MP:0004045 abnormal cell cycle checkpoint function IAGP N RGD:5509061 20191212 MGI PMID:29922180 737295 Rasa3 RAS p21 protein activator 3 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0005152 pancytopenia IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0005344 increased circulating bilirubin level IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20191212 MGI PMID:25705885 737295 Rasa3 RAS p21 protein activator 3 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20200402 MGI 737295 Rasa3 RAS p21 protein activator 3 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20191212 MGI PMID:29922180 737295 Rasa3 RAS p21 protein activator 3 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20191212 MGI PMID:25705885 737295 Rasa3 RAS p21 protein activator 3 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0008816 petechiae IAGP N RGD:5509061 20150416 MGI PMID:2383655 737295 Rasa3 RAS p21 protein activator 3 gene MP:0008850 increased hemoglobin concentration distribution width IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0009246 pale spleen IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0009275 bruising IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0009275 bruising IAGP N RGD:5509061 20150416 MGI PMID:2383655 737295 Rasa3 RAS p21 protein activator 3 gene MP:0009661 abnormal pregnancy IAGP N RGD:5509061 20150416 MGI PMID:2383655 737295 Rasa3 RAS p21 protein activator 3 gene MP:0009676 abnormal hemostasis IAGP N RGD:5509061 20191212 MGI PMID:25705885 737295 Rasa3 RAS p21 protein activator 3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0010067 increased red blood cell distribution width IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0010163 hemolysis IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0010163 hemolysis IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17179160 737295 Rasa3 RAS p21 protein activator 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737295 Rasa3 RAS p21 protein activator 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22773809 737295 Rasa3 RAS p21 protein activator 3 gene MP:0011101 prenatal lethality, incomplete penetrance IAGP N RGD:5509061 20191219 MGI PMID:8334700 737295 Rasa3 RAS p21 protein activator 3 gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20150416 MGI PMID:2383655 737295 Rasa3 RAS p21 protein activator 3 gene MP:0011176 abnormal erythroblast morphology IAGP N RGD:5509061 20191212 MGI PMID:29922180 737295 Rasa3 RAS p21 protein activator 3 gene MP:0011396 abnormal sleep behavior IEA N RGD:5509061 20211021 MGI 737295 Rasa3 RAS p21 protein activator 3 gene MP:0011898 abnormal platelet cell number IAGP N RGD:5509061 20191212 MGI PMID:25705885 737295 Rasa3 RAS p21 protein activator 3 gene MP:0011971 increased circulating lactate dehydrogenase level IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0013293 embryonic lethality prior to tooth bud stage IAGP N RGD:5509061 20210325 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20210520 MGI 737295 Rasa3 RAS p21 protein activator 3 gene MP:0013704 increased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20210401 MGI PMID:33370780 737295 Rasa3 RAS p21 protein activator 3 gene MP:0013776 bone marrow failure IAGP N RGD:5509061 20210401 MGI PMID:33370780 737299 Casq2 calsequestrin 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18583715 737299 Casq2 calsequestrin 2 gene MP:0000278 abnormal myocardial fiber morphology IAGP N RGD:5509061 20141030 MGI PMID:22298808 737299 Casq2 calsequestrin 2 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17607358 737299 Casq2 calsequestrin 2 gene MP:0001785 edema IEA N RGD:5509061 20210520 MGI 737299 Casq2 calsequestrin 2 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17607358 737299 Casq2 calsequestrin 2 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:16932808 737299 Casq2 calsequestrin 2 gene MP:0002953 thick ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:16932808 737299 Casq2 calsequestrin 2 gene MP:0003929 decreased heart rate variability IEA N RGD:5509061 20210128 MGI 737299 Casq2 calsequestrin 2 gene MP:0004088 abnormal sarcoplasmic reticulum morphology IAGP N RGD:5509061 20141030 MGI PMID:22298808 737299 Casq2 calsequestrin 2 gene MP:0004122 abnormal sinus arrhythmia IAGP N RGD:5509061 20141003 MGI PMID:17607358 737299 Casq2 calsequestrin 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:16932808 737299 Casq2 calsequestrin 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:17607358 737299 Casq2 calsequestrin 2 gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:18583715 737299 Casq2 calsequestrin 2 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:17607358 737299 Casq2 calsequestrin 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:16932808 737299 Casq2 calsequestrin 2 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17607358 737299 Casq2 calsequestrin 2 gene MP:0005385 cardiovascular system phenotype IEA N RGD:5509061 20150430 MGI 737299 Casq2 calsequestrin 2 gene MP:0008725 increased heart atrium size IAGP N RGD:5509061 20141003 MGI PMID:17607358 737299 Casq2 calsequestrin 2 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:16932808 737299 Casq2 calsequestrin 2 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:17607358 737299 Casq2 calsequestrin 2 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141003 MGI PMID:18583715 737299 Casq2 calsequestrin 2 gene MP:0008950 ventricular tachycardia IAGP N RGD:5509061 20141030 MGI PMID:22298808 737299 Casq2 calsequestrin 2 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20141003 MGI PMID:17607358 737299 Casq2 calsequestrin 2 gene MP:0009732 ventricular premature beat IAGP N RGD:5509061 20141003 MGI PMID:18583715 737299 Casq2 calsequestrin 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20170105 MGI 737299 Casq2 calsequestrin 2 gene MP:0031633 decreased heart left ventricle muscle contractility IAGP N RGD:5509061 20240704 MGI PMID:17607358 737305 Fetub fetuin beta gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:23562279 737305 Fetub fetuin beta gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:23562279 737305 Fetub fetuin beta gene MP:0003696 abnormal zona pellucida morphology IAGP N RGD:5509061 20141003 MGI PMID:23562279 737310 Ghsr growth hormone secretagogue receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15070777 737310 Ghsr growth hormone secretagogue receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16322794 737310 Ghsr growth hormone secretagogue receptor gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16322794 737310 Ghsr growth hormone secretagogue receptor gene MP:0001663 abnormal digestive system physiology IAGP N RGD:5509061 20141003 MGI PMID:18657539 737310 Ghsr growth hormone secretagogue receptor gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19633195 737310 Ghsr growth hormone secretagogue receptor gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:15070777 737310 Ghsr growth hormone secretagogue receptor gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:16322794 737310 Ghsr growth hormone secretagogue receptor gene MP:0003968 abnormal growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:15070777 737310 Ghsr growth hormone secretagogue receptor gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:15070777 737310 Ghsr growth hormone secretagogue receptor gene MP:0005449 abnormal food intake IAGP N RGD:5509061 20141003 MGI PMID:15070777 737310 Ghsr growth hormone secretagogue receptor gene MP:0005450 abnormal energy expenditure IAGP N RGD:5509061 20141003 MGI PMID:16322794 737310 Ghsr growth hormone secretagogue receptor gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16322794 737310 Ghsr growth hormone secretagogue receptor gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:16322794 737310 Ghsr growth hormone secretagogue receptor gene MP:0008872 abnormal physiological response to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:18657539 737310 Ghsr growth hormone secretagogue receptor gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:16322794 737310 Ghsr growth hormone secretagogue receptor gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:16322794 737310 Ghsr growth hormone secretagogue receptor gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:16322794 737313 Ager advanced glycosylation end product-specific receptor gene MP:0000260 abnormal angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:16873687 737313 Ager advanced glycosylation end product-specific receptor gene MP:0000350 abnormal cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:16873687 737313 Ager advanced glycosylation end product-specific receptor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:16873687 737313 Ager advanced glycosylation end product-specific receptor gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:16936199 737313 Ager advanced glycosylation end product-specific receptor gene MP:0001790 abnormal immune system physiology IAGP N RGD:5509061 20141003 MGI PMID:17003481 737313 Ager advanced glycosylation end product-specific receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16936199 737313 Ager advanced glycosylation end product-specific receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20150101 MGI PMID:11353516 737313 Ager advanced glycosylation end product-specific receptor gene MP:0002706 abnormal kidney size IAGP N RGD:5509061 20141003 MGI PMID:16936199 737313 Ager advanced glycosylation end product-specific receptor gene MP:0002707 abnormal kidney weight IAGP N RGD:5509061 20141003 MGI PMID:12651605 737313 Ager advanced glycosylation end product-specific receptor gene MP:0002733 abnormal thermal nociception IAGP N RGD:5509061 20141003 MGI PMID:15599399 737313 Ager advanced glycosylation end product-specific receptor gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:16936199 737313 Ager advanced glycosylation end product-specific receptor gene MP:0004149 increased bone strength IAGP N RGD:5509061 20141003 MGI PMID:16403440 737313 Ager advanced glycosylation end product-specific receptor gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:12671045 737313 Ager advanced glycosylation end product-specific receptor gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:16403440 737313 Ager advanced glycosylation end product-specific receptor gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:16403440 737313 Ager advanced glycosylation end product-specific receptor gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20141003 MGI PMID:16936199 737313 Ager advanced glycosylation end product-specific receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12651605 737313 Ager advanced glycosylation end product-specific receptor gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:16936199 737313 Ager advanced glycosylation end product-specific receptor gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:16936199 737313 Ager advanced glycosylation end product-specific receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12651605 737313 Ager advanced glycosylation end product-specific receptor gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:16873687 737313 Ager advanced glycosylation end product-specific receptor gene MP:0005595 abnormal vascular smooth muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:12671045 737313 Ager advanced glycosylation end product-specific receptor gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:16403440 737313 Ager advanced glycosylation end product-specific receptor gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16873687 737313 Ager advanced glycosylation end product-specific receptor gene MP:0008124 decreased plasmacytoid dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22367054 737313 Ager advanced glycosylation end product-specific receptor gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20141003 MGI PMID:22367054 737313 Ager advanced glycosylation end product-specific receptor gene MP:0008597 decreased circulating interleukin-6 level IAGP N RGD:5509061 20220922 MGI PMID:16403440 737313 Ager advanced glycosylation end product-specific receptor gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:16403440 737313 Ager advanced glycosylation end product-specific receptor gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:16873687 737313 Ager advanced glycosylation end product-specific receptor gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20141003 MGI PMID:16403440 737313 Ager advanced glycosylation end product-specific receptor gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:16403440 737313 Ager advanced glycosylation end product-specific receptor gene MP:0011338 abnormal mesangial matrix morphology IAGP N RGD:5509061 20141003 MGI PMID:12651605 737313 Ager advanced glycosylation end product-specific receptor gene MP:0011349 abnormal renal glomerulus basement membrane thickness IAGP N RGD:5509061 20141003 MGI PMID:12651605 737313 Ager advanced glycosylation end product-specific receptor gene MP:0013623 increased femur compact bone thickness IAGP N RGD:5509061 20220922 MGI PMID:16403440 737313 Ager advanced glycosylation end product-specific receptor gene MP:0013631 decreased bone trabecular spacing IAGP N RGD:5509061 20220922 MGI PMID:16403440 737313 Ager advanced glycosylation end product-specific receptor gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:16403440 737313 Ager advanced glycosylation end product-specific receptor gene MP:0020416 decreased fibroblast chemotaxis IAGP N RGD:5509061 20170223 MGI PMID:20231695 737313 Ager advanced glycosylation end product-specific receptor gene MP:0031509 decreased vascular smooth muscle cell proliferation IAGP N RGD:5509061 20231109 MGI PMID:12671045 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0001154 seminiferous tubule degeneration IAGP N RGD:5509061 20141003 MGI PMID:12239111 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12239111 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12239111 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12086606 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12239111 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:11698667 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0002891 increased insulin sensitivity IAGP N RGD:5509061 20141003 MGI PMID:12239111 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11698667 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0003960 increased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:12239111 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:12239111 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11698667 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11698667 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:11698667 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:11698667 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:11698667 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:12239111 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0011940 decreased food intake IAGP N RGD:5509061 20141003 MGI PMID:12239111 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0020467 abnormal circadian behavior IAGP N RGD:5509061 20171012 MGI PMID:12086606 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20201015 MGI PMID:26882873 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0020471 abnormal circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:12086606 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0020471 abnormal circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:15071099 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:12086606 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0020472 arrhythmic circadian behavior persistence IAGP N RGD:5509061 20171012 MGI PMID:15071099 737317 Vipr2 vasoactive intestinal peptide receptor 2 gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:12086606 737320 Fxyd5 FXYD domain-containing ion transport regulator 5 gene MP:0004502 decreased incidence of tumors by chemical induction IAGP N RGD:5509061 20220721 MGI PMID:35673579 737320 Fxyd5 FXYD domain-containing ion transport regulator 5 gene MP:0010279 increased gastrointestinal tumor incidence IAGP N RGD:5509061 20220721 MGI PMID:35673579 737330 Pygm muscle glycogen phosphorylase gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20240523 MGI 737330 Pygm muscle glycogen phosphorylase gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230119 MGI 737330 Pygm muscle glycogen phosphorylase gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20240523 MGI 737330 Pygm muscle glycogen phosphorylase gene MP:0003061 decreased aerobic running capacity IAGP N RGD:5509061 20151203 MGI PMID:22730558 737330 Pygm muscle glycogen phosphorylase gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20240523 MGI 737330 Pygm muscle glycogen phosphorylase gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20240523 MGI 737330 Pygm muscle glycogen phosphorylase gene MP:0006034 myoglobinuria IAGP N RGD:5509061 20151203 MGI PMID:22730558 737330 Pygm muscle glycogen phosphorylase gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20151203 MGI PMID:22730558 737330 Pygm muscle glycogen phosphorylase gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20151203 MGI PMID:22730558 737330 Pygm muscle glycogen phosphorylase gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20240523 MGI 737330 Pygm muscle glycogen phosphorylase gene MP:0010401 increased skeletal muscle glycogen level IAGP N RGD:5509061 20151203 MGI PMID:22730558 737330 Pygm muscle glycogen phosphorylase gene MP:0010506 prolonged RR interval IEA N RGD:5509061 20230119 MGI 737330 Pygm muscle glycogen phosphorylase gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 737330 Pygm muscle glycogen phosphorylase gene MP:0020280 increased creatine kinase level IAGP N RGD:5509061 20151203 MGI PMID:22730558 737333 Prg2 proteoglycan 2, bone marrow gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20200402 MGI 737333 Prg2 proteoglycan 2, bone marrow gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:11067904 737333 Prg2 proteoglycan 2, bone marrow gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:11067904 737333 Prg2 proteoglycan 2, bone marrow gene MP:0005061 abnormal eosinophil morphology IAGP N RGD:5509061 20141003 MGI PMID:11067904 737333 Prg2 proteoglycan 2, bone marrow gene MP:0010378 increased respiratory quotient IEA N RGD:5509061 20220519 MGI 737333 Prg2 proteoglycan 2, bone marrow gene MP:0011959 abnormal eye posterior chamber depth IEA N RGD:5509061 20220811 MGI 737335 Sost sclerostin gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:18269310 737335 Sost sclerostin gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19419300 737335 Sost sclerostin gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:19594304 737335 Sost sclerostin gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23918385 737335 Sost sclerostin gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20150507 MGI PMID:24225945 737335 Sost sclerostin gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18269310 737335 Sost sclerostin gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20952383 737335 Sost sclerostin gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22886088 737335 Sost sclerostin gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:18269310 737335 Sost sclerostin gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:23918385 737335 Sost sclerostin gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:22886088 737335 Sost sclerostin gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20150507 MGI PMID:24225945 737335 Sost sclerostin gene MP:0002998 abnormal bone remodeling IAGP N RGD:5509061 20141003 MGI PMID:19419300 737335 Sost sclerostin gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:20952383 737335 Sost sclerostin gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:19594304 737335 Sost sclerostin gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:20952383 737335 Sost sclerostin gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23918385 737335 Sost sclerostin gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20190530 MGI PMID:30622831 737335 Sost sclerostin gene MP:0004149 increased bone strength IAGP N RGD:5509061 20141003 MGI PMID:18269310 737335 Sost sclerostin gene MP:0004149 increased bone strength IAGP N RGD:5509061 20150507 MGI PMID:24225945 737335 Sost sclerostin gene MP:0004348 long femur IAGP N RGD:5509061 20141003 MGI PMID:18269310 737335 Sost sclerostin gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:19419300 737335 Sost sclerostin gene MP:0004986 abnormal osteoblast morphology IAGP N RGD:5509061 20141003 MGI PMID:22886088 737335 Sost sclerostin gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:18269310 737335 Sost sclerostin gene MP:0005006 abnormal osteoblast physiology IAGP N RGD:5509061 20141003 MGI PMID:19419300 737335 Sost sclerostin gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:19419300 737335 Sost sclerostin gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:19594304 737335 Sost sclerostin gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:20952383 737335 Sost sclerostin gene MP:0005605 increased bone mass IAGP N RGD:5509061 20141003 MGI PMID:22886088 737335 Sost sclerostin gene MP:0005605 increased bone mass IAGP N RGD:5509061 20150507 MGI PMID:24225945 737335 Sost sclerostin gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:18269310 737335 Sost sclerostin gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:19594304 737335 Sost sclerostin gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22886088 737335 Sost sclerostin gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19594304 737335 Sost sclerostin gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:18269310 737335 Sost sclerostin gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:20952383 737335 Sost sclerostin gene MP:0010123 increased bone mineral content IAGP N RGD:5509061 20150507 MGI PMID:24225945 737335 Sost sclerostin gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:18269310 737335 Sost sclerostin gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:22886088 737335 Sost sclerostin gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20150507 MGI PMID:24225945 737335 Sost sclerostin gene MP:0010872 increased trabecular bone mass IAGP N RGD:5509061 20150507 MGI PMID:24225945 737335 Sost sclerostin gene MP:0010875 increased bone volume IAGP N RGD:5509061 20141003 MGI PMID:23918385 737335 Sost sclerostin gene MP:0010875 increased bone volume IAGP N RGD:5509061 20150507 MGI PMID:24225945 737335 Sost sclerostin gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:18269310 737335 Sost sclerostin gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:22886088 737335 Sost sclerostin gene MP:0010932 increased trabecular bone connectivity density IAGP N RGD:5509061 20141003 MGI PMID:22886088 737335 Sost sclerostin gene MP:0010961 increased compact bone mass IAGP N RGD:5509061 20150507 MGI PMID:24225945 737335 Sost sclerostin gene MP:0010964 increased compact bone volume IAGP N RGD:5509061 20141003 MGI PMID:18269310 737335 Sost sclerostin gene MP:0010967 increased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:18269310 737335 Sost sclerostin gene MP:0010967 increased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:20952383 737335 Sost sclerostin gene MP:0010967 increased compact bone area IAGP N RGD:5509061 20141003 MGI PMID:22886088 737335 Sost sclerostin gene MP:0013617 increased areal bone mineral density IAGP N RGD:5509061 20220922 MGI PMID:18269310 737335 Sost sclerostin gene MP:0013640 increased bone stiffness IAGP N RGD:5509061 20150507 MGI PMID:24225945 737335 Sost sclerostin gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:18269310 737335 Sost sclerostin gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:19419300 737335 Sost sclerostin gene MP:0020011 increased bone mineral density of femur IAGP N RGD:5509061 20220922 MGI PMID:20952383 737335 Sost sclerostin gene MP:0021191 increased bone mineral density of lumbar vertebrae IAGP N RGD:5509061 20220922 MGI PMID:19594304 737335 Sost sclerostin gene MP:0021191 increased bone mineral density of lumbar vertebrae IAGP N RGD:5509061 20220922 MGI PMID:20952383 737335 Sost sclerostin gene MP:0030442 decreased osteoblast apoptosis IAGP N RGD:5509061 20171221 MGI PMID:19419300 737335 Sost sclerostin gene MP:0030480 decreased osteocyte apoptosis IAGP N RGD:5509061 20171221 MGI PMID:19419300 737335 Sost sclerostin gene MP:0030480 decreased osteocyte apoptosis IAGP N RGD:5509061 20171221 MGI PMID:20952383 737335 Sost sclerostin gene MP:0030482 increased osteocyte number IAGP N RGD:5509061 20171221 MGI PMID:19419300 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:12848940 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0001262 decreased body weight IEA N RGD:5509061 20111116 MGI 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12848940 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:18316356 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:12848940 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:16436610 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20111116 MGI 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0001501 abnormal sleep pattern IAGP N RGD:5509061 20200409 MGI PMID:29016847 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0001898 abnormal long-term depression IAGP N RGD:5509061 20141003 MGI PMID:12848940 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12848940 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0001973 increased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:12848940 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:12848940 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0002207 abnormal long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12848940 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20111116 MGI 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:12848940 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0003008 enhanced long-term potentiation IAGP N RGD:5509061 20141003 MGI PMID:12848940 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0003216 absence seizures IAGP N RGD:5509061 20141003 MGI PMID:18316356 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16436610 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0003546 decreased alcohol consumption IAGP N RGD:5509061 20141003 MGI PMID:16436610 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20200409 MGI PMID:29016847 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0004859 abnormal synaptic plasticity IAGP N RGD:5509061 20141003 MGI PMID:12848940 737337 Gria3 glutamate receptor, ionotropic, AMPA3 (alpha 3) gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12848940 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001116 small gonad IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001116 small gonad IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001119 abnormal female reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:24324164 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001127 small ovary IAGP N RGD:5509061 20141003 MGI PMID:24324164 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220407 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220407 MGI PMID:24324164 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20220407 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001143 constricted vagina orifice IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001146 abnormal testis morphology IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:24324164 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001147 small testis IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001153 small seminiferous tubules IAGP N RGD:5509061 20141003 MGI PMID:24324164 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001155 arrest of spermatogenesis IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220106 MGI PMID:34910520 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:23632635 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001926 female infertility IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:23632635 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001927 abnormal estrous cycle IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001929 abnormal gametogenesis IAGP N RGD:5509061 20141003 MGI PMID:24324164 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0001935 decreased litter size IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002160 abnormal reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18325995 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002286 cryptorchism IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002636 delayed vaginal opening IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002680 decreased corpora lutea number IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002682 decreased mature ovarian follicle number IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:24324164 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002716 small male preputial gland IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:23632635 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002773 decreased circulating luteinizing hormone level IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002780 decreased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:23632635 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002786 abnormal Leydig cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0002790 decreased circulating follicle stimulating hormone level IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0003355 decreased ovulation rate IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0003363 decreased circulating gonadotropin level IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0003507 abnormal ovary physiology IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0003510 decreased circulating dihydrotestosterone level IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0003969 abnormal luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:23632635 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0004855 increased ovary weight IAGP N RGD:5509061 20220106 MGI PMID:34910520 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0004856 decreased ovary weight IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0004884 abnormal testis physiology IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0004930 small epididymis IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005131 increased follicle stimulating hormone level IAGP N RGD:5509061 20220106 MGI PMID:34910520 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005133 increased luteinizing hormone level IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:23632635 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005182 increased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:23632635 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005188 small penis IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005188 small penis IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005189 abnormal anogenital distance IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005250 decreased Sertoli cell number IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:24324164 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0006379 abnormal spermatocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20141003 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0008261 arrest of male meiosis IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:24324164 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0009006 prolonged estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:23632635 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0009009 absent estrous cycle IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0009017 prolonged estrus IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0009020 prolonged metestrus IAGP N RGD:5509061 20141003 MGI PMID:23632635 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0009081 thin uterus IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0009199 abnormal external male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0009205 abnormal internal male genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0009209 abnormal internal female genitalia morphology IAGP N RGD:5509061 20141003 MGI PMID:20068010 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0009234 absent sperm head IAGP N RGD:5509061 20141003 MGI PMID:24324164 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0011128 increased tertiary ovarian follicle number IAGP N RGD:5509061 20141003 MGI PMID:22918878 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0011129 decreased tertiary ovarian follicle number IAGP N RGD:5509061 20220721 MGI PMID:34939930 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0011130 absent tertiary ovarian follicles IAGP N RGD:5509061 20220407 MGI PMID:15625238 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0020869 immotile sperm IAGP N RGD:5509061 20220630 MGI PMID:23340250 737340 Gnrhr gonadotropin releasing hormone receptor gene MP:0031239 increased atretic ovarian follicle number IAGP N RGD:5509061 20220407 MGI PMID:20068010 737342 Cyp24a1 cytochrome P450, family 24, subfamily a, polypeptide 1 gene MP:0000194 increased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:10875271 737342 Cyp24a1 cytochrome P450, family 24, subfamily a, polypeptide 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:10875271 737342 Cyp24a1 cytochrome P450, family 24, subfamily a, polypeptide 1 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10423037 737342 Cyp24a1 cytochrome P450, family 24, subfamily a, polypeptide 1 gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:10875271 737342 Cyp24a1 cytochrome P450, family 24, subfamily a, polypeptide 1 gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:10875271 737342 Cyp24a1 cytochrome P450, family 24, subfamily a, polypeptide 1 gene MP:0005441 increased urine calcium level IAGP N RGD:5509061 20141003 MGI PMID:10875271 737342 Cyp24a1 cytochrome P450, family 24, subfamily a, polypeptide 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:10423037 737342 Cyp24a1 cytochrome P450, family 24, subfamily a, polypeptide 1 gene MP:0011228 abnormal vitamin D level IAGP N RGD:5509061 20141003 MGI PMID:10875271 737344 Pi4kb phosphatidylinositol 4-kinase beta gene MP:0001106 abnormal Schwann cell morphology IAGP N RGD:5509061 20210520 MGI PMID:33106410 737344 Pi4kb phosphatidylinositol 4-kinase beta gene MP:0001405 impaired coordination IAGP N RGD:5509061 20210520 MGI PMID:33106410 737344 Pi4kb phosphatidylinositol 4-kinase beta gene MP:0001406 abnormal gait IAGP N RGD:5509061 20210520 MGI PMID:33106410 737344 Pi4kb phosphatidylinositol 4-kinase beta gene MP:0001513 limb grasping IAGP N RGD:5509061 20210520 MGI PMID:33106410 737344 Pi4kb phosphatidylinositol 4-kinase beta gene MP:0002651 abnormal sciatic nerve morphology IAGP N RGD:5509061 20210520 MGI PMID:33106410 737344 Pi4kb phosphatidylinositol 4-kinase beta gene MP:0008814 decreased nerve conduction velocity IAGP N RGD:5509061 20210520 MGI PMID:33106410 737344 Pi4kb phosphatidylinositol 4-kinase beta gene MP:0010732 abnormal node of Ranvier morphology IAGP N RGD:5509061 20210520 MGI PMID:33106410 737344 Pi4kb phosphatidylinositol 4-kinase beta gene MP:0012051 spasticity IAGP N RGD:5509061 20210520 MGI PMID:33106410 737344 Pi4kb phosphatidylinositol 4-kinase beta gene MP:0020456 decreased myelin sheath amount IAGP N RGD:5509061 20210520 MGI PMID:33106410 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:15183720 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0000084 abnormal fontanelle morphology IAGP N RGD:5509061 20141003 MGI PMID:15183720 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15183720 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0000633 abnormal pituitary gland morphology IAGP N RGD:5509061 20141003 MGI PMID:12907761 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0000636 enlarged pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:12907761 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15183720 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:21251616 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0001377 abnormal mating frequency IAGP N RGD:5509061 20141003 MGI PMID:8573724 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15183720 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:8573724 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15183720 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:15183720 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:8573724 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:15183720 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:15183720 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0003409 decreased width of hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:15183720 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0003817 abnormal pituitary diverticulum morphology IAGP N RGD:5509061 20141003 MGI PMID:12907761 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0004337 clavicle hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:15183720 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:15183720 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0009309 increased small intestine adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21251616 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0009314 increased colon adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:21251616 737346 Tle5 TLE family member 5, transcriptional modulator gene MP:0013342 bifurcated Rathke's pouch IAGP N RGD:5509061 20141204 MGI PMID:12907761 737349 Heph hephaestin gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:5903585 737349 Heph hephaestin gene MP:0000248 macrocytosis IAGP N RGD:5509061 20141003 MGI PMID:5903585 737349 Heph hephaestin gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230601 MGI 737349 Heph hephaestin gene MP:0000274 enlarged heart IEA N RGD:5509061 20230601 MGI 737349 Heph hephaestin gene MP:0000367 abnormal coat/ hair morphology IAGP N RGD:5509061 20141003 MGI PMID:22342521 737349 Heph hephaestin gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20230601 MGI 737349 Heph hephaestin gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:15365174 737349 Heph hephaestin gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20141003 MGI PMID:18326691 737349 Heph hephaestin gene MP:0001326 retina degeneration IAGP N RGD:5509061 20141003 MGI PMID:15365174 737349 Heph hephaestin gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20230601 MGI 737349 Heph hephaestin gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:10932191 737349 Heph hephaestin gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:22342521 737349 Heph hephaestin gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:708646 737349 Heph hephaestin gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:15365174 737349 Heph hephaestin gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:18326691 737349 Heph hephaestin gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:22342521 737349 Heph hephaestin gene MP:0001770 abnormal iron level IAGP N RGD:5509061 20141003 MGI PMID:708646 737349 Heph hephaestin gene MP:0001851 eye inflammation IAGP N RGD:5509061 20141003 MGI PMID:18326691 737349 Heph hephaestin gene MP:0002123 abnormal definitive hematopoiesis IEA N RGD:5509061 20111116 MGI 737349 Heph hephaestin gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20150319 MGI 737349 Heph hephaestin gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20141003 MGI PMID:22342521 737349 Heph hephaestin gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20230601 MGI 737349 Heph hephaestin gene MP:0002447 abnormal erythrocyte morphology IEA N RGD:5509061 20111116 MGI 737349 Heph hephaestin gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:5903585 737349 Heph hephaestin gene MP:0002641 anisopoikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:5903585 737349 Heph hephaestin gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:5903585 737349 Heph hephaestin gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:5903585 737349 Heph hephaestin gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:708646 737349 Heph hephaestin gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:5903585 737349 Heph hephaestin gene MP:0004151 decreased circulating iron level IAGP N RGD:5509061 20141003 MGI PMID:22342521 737349 Heph hephaestin gene MP:0004265 abnormal placental transport IAGP N RGD:5509061 20141003 MGI PMID:708646 737349 Heph hephaestin gene MP:0005097 polychromatophilia IAGP N RGD:5509061 20141003 MGI PMID:5903585 737349 Heph hephaestin gene MP:0005098 abnormal optic choroid morphology IAGP N RGD:5509061 20141003 MGI PMID:15365174 737349 Heph hephaestin gene MP:0005103 abnormal retina pigmentation IAGP N RGD:5509061 20141003 MGI PMID:15365174 737349 Heph hephaestin gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:15365174 737349 Heph hephaestin gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:18326691 737349 Heph hephaestin gene MP:0005201 abnormal retina pigment epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:22342521 737349 Heph hephaestin gene MP:0005239 abnormal Bruch membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:18326691 737349 Heph hephaestin gene MP:0005343 increased circulating aspartate transaminase level IEA N RGD:5509061 20230601 MGI 737349 Heph hephaestin gene MP:0005548 retina pigment epithelium atrophy IAGP N RGD:5509061 20141003 MGI PMID:22342521 737349 Heph hephaestin gene MP:0005549 retina pigment epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:15365174 737349 Heph hephaestin gene MP:0005549 retina pigment epithelium hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18326691 737349 Heph hephaestin gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:5903585 737349 Heph hephaestin gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:180329 737349 Heph hephaestin gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20111116 MGI 737349 Heph hephaestin gene MP:0008387 hypochromic anemia IAGP N RGD:5509061 20141003 MGI PMID:5903585 737349 Heph hephaestin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:15365174 737349 Heph hephaestin gene MP:0008469 abnormal protein level IAGP N RGD:5509061 20141003 MGI PMID:22342521 737349 Heph hephaestin gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:10791995 737349 Heph hephaestin gene MP:0008810 increased circulating iron level IEA N RGD:5509061 20230601 MGI 737349 Heph hephaestin gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:15365174 737349 Heph hephaestin gene MP:0008852 retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:18326691 737349 Heph hephaestin gene MP:0011188 increased erythrocyte protoporphyrin level IAGP N RGD:5509061 20141003 MGI PMID:658175 737349 Heph hephaestin gene MP:0014175 abnormal ciliary epithelium morphology IAGP N RGD:5509061 20160505 MGI PMID:18326691 737349 Heph hephaestin gene MP:0020369 increased intestinal iron level IAGP N RGD:5509061 20161020 MGI PMID:10791995 737349 Heph hephaestin gene MP:0031606 increased susceptibility to age-related retinal degeneration IAGP N RGD:5509061 20240404 MGI PMID:18326691 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:11986200 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:18453616 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:18453616 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0000222 decreased neutrophil cell number IAGP N RGD:5509061 20141003 MGI PMID:18453616 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:11986200 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:11986200 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0000556 abnormal hindlimb morphology IAGP N RGD:5509061 20141003 MGI PMID:17293482 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:11986200 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11986200 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0001204 decreased sensitivity to skin irradiation IAGP N RGD:5509061 20141003 MGI PMID:18787106 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:19276363 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0001585 hemolytic anemia IAGP N RGD:5509061 20141003 MGI PMID:11986200 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0001829 increased activated T cell number IAGP N RGD:5509061 20141003 MGI PMID:24021673 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:19276363 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11986200 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18453616 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8864123 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0002463 abnormal neutrophil physiology IAGP N RGD:5509061 20141003 MGI PMID:8864123 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0002467 impaired neutrophil phagocytosis IAGP N RGD:5509061 20141003 MGI PMID:8864123 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:20685990 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:19284971 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:11986200 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0002799 abnormal passive avoidance behavior IAGP N RGD:5509061 20141003 MGI PMID:10541465 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:18453616 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0002912 abnormal excitatory postsynaptic potential IAGP N RGD:5509061 20141003 MGI PMID:10541465 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20141003 MGI PMID:15665111 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:17293482 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:19276363 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:18787106 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0004875 increased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19284971 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17126807 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0004993 decreased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:19276363 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:24021673 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:8864123 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0005074 impaired granulocyte bactericidal activity IAGP N RGD:5509061 20141003 MGI PMID:8864123 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:17135401 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:15665111 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:17293482 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0005673 decreased susceptibility to graft versus host disease IAGP N RGD:5509061 20141003 MGI PMID:24021673 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0006036 abnormal mitochondrial physiology IAGP N RGD:5509061 20141003 MGI PMID:17293482 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0006080 brain ischemia IAGP N RGD:5509061 20141003 MGI PMID:19233173 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19284971 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19284971 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24021673 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:24021673 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:17135401 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:19276363 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0008464 absent peripheral lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:24021673 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:18453616 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0008719 impaired neutrophil recruitment IAGP N RGD:5509061 20141003 MGI PMID:19233173 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0008720 impaired neutrophil chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:8864123 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0008752 abnormal tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:18453616 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:11986200 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:19276363 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:8864123 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0009789 decreased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:18453616 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0010334 pleural effusion IAGP N RGD:5509061 20141003 MGI PMID:18453616 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20141003 MGI PMID:19276363 737351 Cd47 CD47 antigen (Rh-related antigen, integrin-associated signal transducer) gene MP:0020934 increased susceptibility to Retroviridae infection IAGP N RGD:5509061 20200430 MGI PMID:24021673 737352 Pde5a phosphodiesterase 5A, cGMP-specific gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 737352 Pde5a phosphodiesterase 5A, cGMP-specific gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 737352 Pde5a phosphodiesterase 5A, cGMP-specific gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20210520 MGI 737352 Pde5a phosphodiesterase 5A, cGMP-specific gene MP:0000691 enlarged spleen IEA N RGD:5509061 20210520 MGI 737352 Pde5a phosphodiesterase 5A, cGMP-specific gene MP:0001258 decreased body length IEA N RGD:5509061 20210826 MGI 737352 Pde5a phosphodiesterase 5A, cGMP-specific gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20191114 MGI PMID:29341896 737352 Pde5a phosphodiesterase 5A, cGMP-specific gene MP:0002759 abnormal caudal vertebrae morphology IEA N RGD:5509061 20220811 MGI 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:21982707 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21982707 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:21982707 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:21982707 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:21982707 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:21982707 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:21982707 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:21982707 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:21982707 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0004988 increased osteoblast cell number IAGP N RGD:5509061 20141003 MGI PMID:21982707 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:21982707 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20141003 MGI PMID:21982707 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:21982707 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0010868 increased bone trabecula number IAGP N RGD:5509061 20141003 MGI PMID:21982707 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0010876 decreased bone volume IAGP N RGD:5509061 20141003 MGI PMID:21982707 737358 Inpp4b inositol polyphosphate-4-phosphatase, type II gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:21982707 737365 Pde2a phosphodiesterase 2A, cGMP-stimulated gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20201022 MGI 737365 Pde2a phosphodiesterase 2A, cGMP-stimulated gene MP:0002833 increased heart weight IEA N RGD:5509061 20211021 MGI 737365 Pde2a phosphodiesterase 2A, cGMP-stimulated gene MP:0005344 increased circulating bilirubin level IEA N RGD:5509061 20211021 MGI 737365 Pde2a phosphodiesterase 2A, cGMP-stimulated gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19506089 737365 Pde2a phosphodiesterase 2A, cGMP-stimulated gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737365 Pde2a phosphodiesterase 2A, cGMP-stimulated gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20141003 MGI 737366 Qtrt1 queuine tRNA-ribosyltransferase catalytic subunit 1 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20141003 MGI PMID:21487017 737366 Qtrt1 queuine tRNA-ribosyltransferase catalytic subunit 1 gene MP:0013724 decreased circulating tyrosine level IAGP N RGD:5509061 20150409 MGI PMID:21487017 737373 Fut1 fucosyltransferase 1 gene MP:0002059 abnormal seminal vesicle morphology IEA N RGD:5509061 20181227 MGI 737373 Fut1 fucosyltransferase 1 gene MP:0002691 small stomach IEA N RGD:5509061 20181227 MGI 737373 Fut1 fucosyltransferase 1 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:14967068 737373 Fut1 fucosyltransferase 1 gene MP:0003698 abnormal male reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:11713270 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:19668367 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0001192 scaly skin IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0001194 dermatitis IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0001200 thick skin IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0001212 skin lesions IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0001214 skin hyperplasia IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0001242 hyperkeratosis IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:20826752 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:22075698 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:21435587 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:21435587 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:20808283 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0002083 premature death IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:21435587 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10626892 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0002405 respiratory system inflammation IAGP N RGD:5509061 20141003 MGI PMID:22075698 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0002656 abnormal keratinocyte differentiation IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:21435587 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0003413 hair follicle degeneration IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:21435587 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0004800 decreased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:24166976 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0004803 increased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:23569233 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19668367 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0004972 abnormal regulatory T cell number IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19668367 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:21435587 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0004974 decreased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:19668367 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:19668367 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10586044 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10975814 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:19668367 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:24166976 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0005114 premature hair loss IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:21435587 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0005150 cachexia IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10626892 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0005463 abnormal CD4-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10975814 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:11157058 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0005597 decreased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:11157058 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0008086 increased T-helper 1 cell number IAGP N RGD:5509061 20141003 MGI PMID:21435587 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0008088 abnormal T-helper 1 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20808283 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0008092 abnormal T-helper 2 cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:20808283 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0008177 increased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:20826752 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0008178 decreased germinal center B cell number IAGP N RGD:5509061 20141003 MGI PMID:20826752 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0008482 decreased spleen germinal center number IAGP N RGD:5509061 20141003 MGI PMID:20826752 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0008495 decreased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20826752 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:20826752 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:20808283 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0008673 decreased interleukin-13 secretion IAGP N RGD:5509061 20141003 MGI PMID:20808283 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0008700 decreased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:20808283 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0008703 decreased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:20808283 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0008883 abnormal enterocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:21435587 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20151217 MGI PMID:26099023 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0010186 increased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:20826752 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0010187 decreased T follicular helper cell number IAGP N RGD:5509061 20141003 MGI PMID:20826752 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:21435587 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0010220 decreased T-helper 17 cell number IAGP N RGD:5509061 20141003 MGI PMID:24166976 737375 Tnfrsf4 tumor necrosis factor receptor superfamily, member 4 gene MP:0011156 abnormal hypodermis fat layer morphology IAGP N RGD:5509061 20151217 MGI PMID:26099023 737377 B4galt6 UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 6 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 737377 B4galt6 UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 6 gene MP:0005621 abnormal cell physiology IAGP N RGD:5509061 20180503 MGI PMID:23882130 737382 Gpx3 glutathione peroxidase 3 gene MP:0000249 abnormal blood vessel physiology IAGP N RGD:5509061 20141003 MGI PMID:21518981 737382 Gpx3 glutathione peroxidase 3 gene MP:0001775 abnormal selenium level IAGP N RGD:5509061 20141003 MGI PMID:20015939 737382 Gpx3 glutathione peroxidase 3 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 737382 Gpx3 glutathione peroxidase 3 gene MP:0005607 decreased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:21518981 737382 Gpx3 glutathione peroxidase 3 gene MP:0006058 decreased cerebral infarct size IAGP N RGD:5509061 20141003 MGI PMID:21518981 737382 Gpx3 glutathione peroxidase 3 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20141003 MGI PMID:21518981 737382 Gpx3 glutathione peroxidase 3 gene MP:0009586 increased platelet aggregation IAGP N RGD:5509061 20141003 MGI PMID:21518981 737382 Gpx3 glutathione peroxidase 3 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21518981 737382 Gpx3 glutathione peroxidase 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:21518981 737382 Gpx3 glutathione peroxidase 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737382 Gpx3 glutathione peroxidase 3 gene MP:0011603 decreased glutathione peroxidase activity IAGP N RGD:5509061 20141003 MGI PMID:20015939 737382 Gpx3 glutathione peroxidase 3 gene MP:0013294 prenatal lethality prior to heart atrial septation IEA N RGD:5509061 20201231 MGI 737382 Gpx3 glutathione peroxidase 3 gene MP:0031121 increased susceptibility to induced thrombosis IAGP N RGD:5509061 20200924 MGI PMID:21518981 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:12101101 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0000761 thin diaphragm muscle IAGP N RGD:5509061 20141003 MGI PMID:21305030 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0000937 abnormal motor neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18226545 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:12101101 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:21305030 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0001078 abnormal phrenic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:15905852 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0001404 no spontaneous movement IAGP N RGD:5509061 20141003 MGI PMID:21305030 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0001429 dehydration IAGP N RGD:5509061 20141003 MGI PMID:12101101 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:12101101 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0001512 trunk curl IAGP N RGD:5509061 20141003 MGI PMID:21305030 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:12101101 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:21305030 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0001951 abnormal breathing pattern IAGP N RGD:5509061 20141003 MGI PMID:12101101 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0002095 abnormal skin pigmentation IAGP N RGD:5509061 20141003 MGI PMID:21305030 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:12101101 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:12101101 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0002882 abnormal neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:18226545 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0002914 abnormal endplate potential IAGP N RGD:5509061 20141003 MGI PMID:15905852 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12101101 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:12101101 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0004835 abnormal miniature endplate potential IAGP N RGD:5509061 20141003 MGI PMID:21305030 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0005192 increased motor neuron number IAGP N RGD:5509061 20141003 MGI PMID:18226545 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:18226545 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0008415 abnormal neurite morphology IAGP N RGD:5509061 20141003 MGI PMID:18226545 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:12101101 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12101101 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21305030 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12101101 737384 Chrng cholinergic receptor, nicotinic, gamma polypeptide gene MP:0012055 abnormal phrenic nerve innervation pattern to diaphragm IAGP N RGD:5509061 20141003 MGI PMID:15905852 737389 Dpysl2 dihydropyrimidinase-like 2 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:22279220 737389 Dpysl2 dihydropyrimidinase-like 2 gene MP:0009969 abnormal cerebral cortex pyramidal cell morphology IAGP N RGD:5509061 20141003 MGI PMID:22279220 737393 Pdc phosducin gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0002546 mydriasis IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0002975 vascular smooth muscle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0003025 increased vasoconstriction IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20141003 MGI PMID:14973130 737393 Pdc phosducin gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0005591 decreased vasodilation IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0005600 increased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0005665 increased circulating noradrenaline level IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0006143 increased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0006144 increased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20141003 MGI PMID:18367617 737393 Pdc phosducin gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:19959875 737393 Pdc phosducin gene MP:0011478 abnormal urine catecholamine level IAGP N RGD:5509061 20141003 MGI PMID:19959875 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0000102 abnormal nasal bone morphology IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0000120 malocclusion IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0000484 abnormal pulmonary artery morphology IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0000550 abnormal forelimb morphology IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0001290 delayed eyelid opening IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0001340 abnormal eyelid morphology IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0001348 abnormal lacrimal gland physiology IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22414809 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0002110 abnormal digit morphology IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0002114 abnormal axial skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0002161 abnormal fertility/fecundity IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0002233 abnormal nose morphology IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0004263 abnormal limb posture IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0005287 narrow eye opening IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0008489 slow postnatal weight gain IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:22414809 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0010899 abnormal pulmonary alveolar system morphology IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0011641 abnormal pulmonary collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0011939 increased food intake IAGP N RGD:5509061 20141003 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0030622 increased cysteine level IAGP N RGD:5509061 20180913 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0030623 decreased cysteine level IAGP N RGD:5509061 20180920 MGI PMID:22414809 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0030625 increased circulating cysteine level IAGP N RGD:5509061 20180913 MGI PMID:21693692 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0030626 decreased circulating cysteine level IAGP N RGD:5509061 20180920 MGI PMID:22414809 737395 Cdo1 cysteine dioxygenase 1, cytosolic gene MP:0030636 decreased taurine level IAGP N RGD:5509061 20180913 MGI PMID:21693692 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20141003 MGI PMID:11266438 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0000490 abnormal crypts of Lieberkuhn morphology IAGP N RGD:5509061 20141003 MGI PMID:15705887 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0000495 abnormal colon morphology IAGP N RGD:5509061 20141003 MGI PMID:15705887 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0000527 abnormal kidney development IAGP N RGD:5509061 20141003 MGI PMID:11266438 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:11266438 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:11266438 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:11266438 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11266438 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11266438 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11266438 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0001764 abnormal homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15705887 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:11266438 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0002396 abnormal hematopoietic system morphology/development IAGP N RGD:5509061 20141003 MGI PMID:11266438 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:11266438 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:11266438 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11266438 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:11266438 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0008873 increased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:15705887 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11266438 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15705887 737400 Slc19a1 solute carrier family 19 (folate transporter), member 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11266438 737403 Pawr PRKC, apoptosis, WT1, regulator gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:12970181 737403 Pawr PRKC, apoptosis, WT1, regulator gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12970181 737403 Pawr PRKC, apoptosis, WT1, regulator gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20230601 MGI 737403 Pawr PRKC, apoptosis, WT1, regulator gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16585168 737403 Pawr PRKC, apoptosis, WT1, regulator gene MP:0002573 behavioral despair IAGP N RGD:5509061 20141003 MGI PMID:16051151 737403 Pawr PRKC, apoptosis, WT1, regulator gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:12970181 737403 Pawr PRKC, apoptosis, WT1, regulator gene MP:0005154 increased B cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12970181 737403 Pawr PRKC, apoptosis, WT1, regulator gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:12970181 737403 Pawr PRKC, apoptosis, WT1, regulator gene MP:0005466 abnormal T-helper 2 physiology IAGP N RGD:5509061 20141003 MGI PMID:12970181 737403 Pawr PRKC, apoptosis, WT1, regulator gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20160421 MGI 737403 Pawr PRKC, apoptosis, WT1, regulator gene MP:0008944 decreased sensitivity to induced cell death IAGP N RGD:5509061 20150212 MGI PMID:12634851 737403 Pawr PRKC, apoptosis, WT1, regulator gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 737404 Coq3 coenzyme Q3 methyltransferase gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20201022 MGI 737404 Coq3 coenzyme Q3 methyltransferase gene MP:0001529 abnormal vocalization IEA N RGD:5509061 20201022 MGI 737404 Coq3 coenzyme Q3 methyltransferase gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 737404 Coq3 coenzyme Q3 methyltransferase gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20190926 MGI PMID:23045551 737404 Coq3 coenzyme Q3 methyltransferase gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737404 Coq3 coenzyme Q3 methyltransferase gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 737406 Mob4 MOB family member 4, phocein gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20240926 MGI 737406 Mob4 MOB family member 4, phocein gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20240926 MGI 737406 Mob4 MOB family member 4, phocein gene MP:0001698 decreased embryo size IEA N RGD:5509061 20240926 MGI 737406 Mob4 MOB family member 4, phocein gene MP:0003085 abnormal egg cylinder morphology IEA N RGD:5509061 20240926 MGI 737406 Mob4 MOB family member 4, phocein gene MP:0009331 absent primitive node IEA N RGD:5509061 20240926 MGI 737406 Mob4 MOB family member 4, phocein gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 737406 Mob4 MOB family member 4, phocein gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20231207 MGI 737406 Mob4 MOB family member 4, phocein gene MP:0012724 absent head fold IEA N RGD:5509061 20240926 MGI 737406 Mob4 MOB family member 4, phocein gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20230601 MGI 737408 Ddx39b DEAD box helicase 39b gene MP:0001658 increased mortality induced by gamma-irradiation IAGP N RGD:5509061 20210325 MGI PMID:32989256 737408 Ddx39b DEAD box helicase 39b gene MP:0002007 increased cellular sensitivity to gamma-irradiation IAGP N RGD:5509061 20210325 MGI PMID:32989256 737408 Ddx39b DEAD box helicase 39b gene MP:0011110 preweaning lethality, incomplete penetrance IAGP N RGD:5509061 20210325 MGI PMID:32989256 737412 Aqp8 aquaporin 8 gene MP:0000623 decreased salivation IAGP N RGD:5509061 20141003 MGI PMID:15647389 737412 Aqp8 aquaporin 8 gene MP:0001130 abnormal ovarian folliculogenesis IAGP N RGD:5509061 20220505 MGI PMID:21117174 737412 Aqp8 aquaporin 8 gene MP:0001148 enlarged testis IAGP N RGD:5509061 20141003 MGI PMID:15647389 737412 Aqp8 aquaporin 8 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:15647389 737412 Aqp8 aquaporin 8 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:15647389 737412 Aqp8 aquaporin 8 gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20141003 MGI PMID:15647389 737412 Aqp8 aquaporin 8 gene MP:0001784 abnormal fluid regulation IAGP N RGD:5509061 20220505 MGI PMID:21117174 737412 Aqp8 aquaporin 8 gene MP:0001928 abnormal ovulation IAGP N RGD:5509061 20220505 MGI PMID:21117174 737412 Aqp8 aquaporin 8 gene MP:0001934 increased litter size IAGP N RGD:5509061 20220505 MGI PMID:21117174 737412 Aqp8 aquaporin 8 gene MP:0002681 increased corpora lutea number IAGP N RGD:5509061 20220505 MGI PMID:21117174 737412 Aqp8 aquaporin 8 gene MP:0002988 decreased urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:15647389 737412 Aqp8 aquaporin 8 gene MP:0004851 increased testis weight IAGP N RGD:5509061 20141003 MGI PMID:15647389 737412 Aqp8 aquaporin 8 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:15647389 737412 Aqp8 aquaporin 8 gene MP:0031016 decreased granulosa cell apoptosis IAGP N RGD:5509061 20220505 MGI PMID:21117174 737412 Aqp8 aquaporin 8 gene MP:0031411 increased ovulation rate IAGP N RGD:5509061 20220630 MGI PMID:21117174 737412 Aqp8 aquaporin 8 gene MP:0031421 increased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:21117174 737412 Aqp8 aquaporin 8 gene MP:0031424 enhanced female fertility IAGP N RGD:5509061 20220714 MGI PMID:21117174 737414 Cdh1 cadherin 1 gene MP:0000379 decreased hair follicle number IAGP N RGD:5509061 20141003 MGI PMID:18809908 737414 Cdh1 cadherin 1 gene MP:0001191 abnormal skin condition IAGP N RGD:5509061 20141003 MGI PMID:18809908 737414 Cdh1 cadherin 1 gene MP:0001195 flaky skin IAGP N RGD:5509061 20141003 MGI PMID:18809908 737414 Cdh1 cadherin 1 gene MP:0001196 shiny skin IAGP N RGD:5509061 20141003 MGI PMID:18809908 737414 Cdh1 cadherin 1 gene MP:0001198 tight skin IAGP N RGD:5509061 20141003 MGI PMID:18809908 737414 Cdh1 cadherin 1 gene MP:0001208 blistering IAGP N RGD:5509061 20141003 MGI PMID:18809908 737414 Cdh1 cadherin 1 gene MP:0001216 abnormal epidermal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18809908 737414 Cdh1 cadherin 1 gene MP:0001219 thick epidermis IAGP N RGD:5509061 20141003 MGI PMID:18809908 737414 Cdh1 cadherin 1 gene MP:0001231 abnormal epidermis stratum basale morphology IAGP N RGD:5509061 20141003 MGI PMID:18809908 737414 Cdh1 cadherin 1 gene MP:0001233 abnormal epidermis suprabasal layer morphology IAGP N RGD:5509061 20141003 MGI PMID:18809908 737414 Cdh1 cadherin 1 gene MP:0001236 abnormal epidermis stratum spinosum morphology IAGP N RGD:5509061 20141003 MGI PMID:18809908 737414 Cdh1 cadherin 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:17097565 737414 Cdh1 cadherin 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20150514 MGI PMID:24784840 737414 Cdh1 cadherin 1 gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20190523 MGI PMID:21282721 737414 Cdh1 cadherin 1 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:23354125 737414 Cdh1 cadherin 1 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20141003 MGI PMID:17138661 737414 Cdh1 cadherin 1 gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20141003 MGI PMID:20652949 737414 Cdh1 cadherin 1 gene MP:0001715 placental labyrinth hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:20652949 737414 Cdh1 cadherin 1 gene MP:0001722 pale yolk sac IAGP N RGD:5509061 20141003 MGI PMID:20652949 737414 Cdh1 cadherin 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:20652949 737414 Cdh1 cadherin 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17097565 737414 Cdh1 cadherin 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20150514 MGI PMID:24784840 737414 Cdh1 cadherin 1 gene MP:0001883 increased mammary adenocarcinoma incidence IAGP N RGD:5509061 20190523 MGI PMID:21282721 737414 Cdh1 cadherin 1 gene MP:0002013 increased pilomatricoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17097565 737414 Cdh1 cadherin 1 gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:15673570 737414 Cdh1 cadherin 1 gene MP:0002083 premature death IAGP N RGD:5509061 20150514 MGI PMID:24784840 737414 Cdh1 cadherin 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:17138661 737414 Cdh1 cadherin 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8058792 737414 Cdh1 cadherin 1 gene MP:0002086 abnormal extraembryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:8058792 737414 Cdh1 cadherin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17097565 737414 Cdh1 cadherin 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:20652949 737414 Cdh1 cadherin 1 gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:18806773 737414 Cdh1 cadherin 1 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:17138661 737414 Cdh1 cadherin 1 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:22479204 737414 Cdh1 cadherin 1 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:7846066 737414 Cdh1 cadherin 1 gene MP:0002663 absent blastocoele IAGP N RGD:5509061 20141003 MGI PMID:8058792 737414 Cdh1 cadherin 1 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20141003 MGI PMID:18809908 737414 Cdh1 cadherin 1 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:11040191 737414 Cdh1 cadherin 1 gene MP:0002957 increased intestinal adenocarcinoma incidence IAGP N RGD:5509061 20150514 MGI PMID:24784840 737414 Cdh1 cadherin 1 gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:23354125 737414 Cdh1 cadherin 1 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:12049767 737414 Cdh1 cadherin 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:17138661 737414 Cdh1 cadherin 1 gene MP:0003694 failure of blastocyst to hatch from the zona pellucida IAGP N RGD:5509061 20141003 MGI PMID:7846066 737414 Cdh1 cadherin 1 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:20652949 737414 Cdh1 cadherin 1 gene MP:0004047 abnormal milk composition IAGP N RGD:5509061 20141003 MGI PMID:12049767 737414 Cdh1 cadherin 1 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17097565 737414 Cdh1 cadherin 1 gene MP:0004207 increased squamous cell carcinoma incidence IAGP N RGD:5509061 20150514 MGI PMID:24784840 737414 Cdh1 cadherin 1 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:17138661 737414 Cdh1 cadherin 1 gene MP:0005028 abnormal trophectoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:22479204 737414 Cdh1 cadherin 1 gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20141003 MGI PMID:20652949 737414 Cdh1 cadherin 1 gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20141003 MGI PMID:23354125 737414 Cdh1 cadherin 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:23354125 737414 Cdh1 cadherin 1 gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:18809908 737414 Cdh1 cadherin 1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:12049767 737414 Cdh1 cadherin 1 gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20190523 MGI PMID:21282721 737414 Cdh1 cadherin 1 gene MP:0006270 abnormal mammary gland growth during lactation IAGP N RGD:5509061 20141003 MGI PMID:12049767 737414 Cdh1 cadherin 1 gene MP:0008010 increased gastric adenocarcinoma incidence IAGP N RGD:5509061 20150514 MGI PMID:24784840 737414 Cdh1 cadherin 1 gene MP:0008803 abnormal placental labyrinth vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20652949 737414 Cdh1 cadherin 1 gene MP:0008882 abnormal enterocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:18806773 737414 Cdh1 cadherin 1 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:23354125 737414 Cdh1 cadherin 1 gene MP:0009311 increased duodenum adenocarcinoma incidence IAGP N RGD:5509061 20150514 MGI PMID:24784840 737414 Cdh1 cadherin 1 gene MP:0009503 abnormal mammary gland duct morphology IAGP N RGD:5509061 20190523 MGI PMID:21282721 737414 Cdh1 cadherin 1 gene MP:0009505 abnormal mammary gland lobule morphology IAGP N RGD:5509061 20190523 MGI PMID:21282721 737414 Cdh1 cadherin 1 gene MP:0009687 empty decidua capsularis IAGP N RGD:5509061 20141003 MGI PMID:17138661 737414 Cdh1 cadherin 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:18809908 737414 Cdh1 cadherin 1 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:7846066 737414 Cdh1 cadherin 1 gene MP:0010038 abnormal placenta physiology IAGP N RGD:5509061 20141003 MGI PMID:20652949 737414 Cdh1 cadherin 1 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:17097565 737414 Cdh1 cadherin 1 gene MP:0010249 lactation failure IAGP N RGD:5509061 20150409 MGI PMID:12049767 737414 Cdh1 cadherin 1 gene MP:0010249 lactation failure IAGP N RGD:5509061 20190523 MGI PMID:21282721 737414 Cdh1 cadherin 1 gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20190523 MGI PMID:21282721 737414 Cdh1 cadherin 1 gene MP:0010300 increased skin tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:17097565 737414 Cdh1 cadherin 1 gene MP:0010301 increased stomach tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:11040191 737414 Cdh1 cadherin 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18809908 737414 Cdh1 cadherin 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15673570 737414 Cdh1 cadherin 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7846066 737414 Cdh1 cadherin 1 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:8058792 737414 Cdh1 cadherin 1 gene MP:0011096 embryonic lethality between implantation and somite formation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17138661 737414 Cdh1 cadherin 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20652949 737414 Cdh1 cadherin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737414 Cdh1 cadherin 1 gene MP:0011521 decreased placental labyrinth size IAGP N RGD:5509061 20141003 MGI PMID:20652949 737414 Cdh1 cadherin 1 gene MP:0011819 increased pancreatic beta cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:23354125 737414 Cdh1 cadherin 1 gene MP:0012102 absent trophectoderm IAGP N RGD:5509061 20141003 MGI PMID:17138661 737414 Cdh1 cadherin 1 gene MP:0012102 absent trophectoderm IAGP N RGD:5509061 20141003 MGI PMID:22479204 737414 Cdh1 cadherin 1 gene MP:0012102 absent trophectoderm IAGP N RGD:5509061 20141003 MGI PMID:8058792 737414 Cdh1 cadherin 1 gene MP:0012111 failure of morula compaction IAGP N RGD:5509061 20141003 MGI PMID:7846066 737414 Cdh1 cadherin 1 gene MP:0012119 increased trophectoderm apoptosis IAGP N RGD:5509061 20141003 MGI PMID:22479204 737414 Cdh1 cadherin 1 gene MP:0013716 hypolactation IAGP N RGD:5509061 20190523 MGI PMID:21282721 737417 Cdc42bpb CDC42 binding protein kinase beta gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210520 MGI 737417 Cdc42bpb CDC42 binding protein kinase beta gene MP:0003717 pallor IEA N RGD:5509061 20210520 MGI 737417 Cdc42bpb CDC42 binding protein kinase beta gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 737419 Sema6c sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6C gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20220811 MGI 737419 Sema6c sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6C gene MP:0000274 enlarged heart IEA N RGD:5509061 20220811 MGI 737419 Sema6c sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6C gene MP:0000494 abnormal cecum morphology IEA N RGD:5509061 20210520 MGI 737419 Sema6c sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6C gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20210520 MGI 737419 Sema6c sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6C gene MP:0000601 small liver IEA N RGD:5509061 20210520 MGI 737419 Sema6c sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6C gene MP:0003998 decreased thermal nociceptive threshold IEA N RGD:5509061 20111116 MGI 737419 Sema6c sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6C gene MP:0005084 abnormal gallbladder morphology IEA N RGD:5509061 20220811 MGI 737419 Sema6c sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6C gene MP:0009476 enlarged cecum IEA N RGD:5509061 20210520 MGI 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20161103 MGI PMID:27058611 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20160421 MGI PMID:25536025 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22460952 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:22460952 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22460952 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20220811 MGI 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22460952 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0009747 impaired behavioral response to xenobiotic IAGP N RGD:5509061 20160421 MGI PMID:25536025 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:22460952 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0010404 ostium primum atrial septal defect IAGP N RGD:5509061 20161103 MGI PMID:27058611 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20161103 MGI PMID:27058611 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0010419 inlet ventricular septal defect IAGP N RGD:5509061 20161103 MGI PMID:27058611 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0010607 common atrioventricular valve IAGP N RGD:5509061 20161103 MGI PMID:27058611 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20161103 MGI PMID:27058611 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20141003 MGI 737422 Nr1d2 nuclear receptor subfamily 1, group D, member 2 gene MP:0020470 shortened circadian behavior period IAGP N RGD:5509061 20171012 MGI PMID:22460952 737423 Pip prolactin induced protein gene MP:0000351 increased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20052012 737423 Pip prolactin induced protein gene MP:0000511 abnormal intestinal mucosa morphology IAGP N RGD:5509061 20141003 MGI PMID:20052012 737423 Pip prolactin induced protein gene MP:0000709 enlarged thymus IAGP N RGD:5509061 20141003 MGI PMID:20052012 737423 Pip prolactin induced protein gene MP:0002742 enlarged submandibular lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:20052012 737423 Pip prolactin induced protein gene MP:0002816 colitis IAGP N RGD:5509061 20141003 MGI PMID:20052012 737423 Pip prolactin induced protein gene MP:0002941 increased circulating alanine transaminase level IEA N RGD:5509061 20231207 MGI 737423 Pip prolactin induced protein gene MP:0006042 increased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20052012 737423 Pip prolactin induced protein gene MP:0009381 abnormal prostate gland dorsolateral lobe morphology IAGP N RGD:5509061 20141003 MGI PMID:20052012 737423 Pip prolactin induced protein gene MP:0009543 abnormal thymus corticomedullary boundary morphology IAGP N RGD:5509061 20141003 MGI PMID:20052012 737423 Pip prolactin induced protein gene MP:0010138 arteritis IAGP N RGD:5509061 20141003 MGI PMID:20052012 737423 Pip prolactin induced protein gene MP:0013590 enlarged thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:20052012 737425 Git1 GIT ArfGAP 1 gene MP:0001176 abnormal lung development IAGP N RGD:5509061 20141003 MGI PMID:19273721 737425 Git1 GIT ArfGAP 1 gene MP:0001182 lung hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:19273721 737425 Git1 GIT ArfGAP 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:19383529 737425 Git1 GIT ArfGAP 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21499268 737425 Git1 GIT ArfGAP 1 gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:19383529 737425 Git1 GIT ArfGAP 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:21499268 737425 Git1 GIT ArfGAP 1 gene MP:0001458 abnormal object recognition memory IAGP N RGD:5509061 20141003 MGI PMID:21499268 737425 Git1 GIT ArfGAP 1 gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:21499268 737425 Git1 GIT ArfGAP 1 gene MP:0001522 impaired swimming IAGP N RGD:5509061 20141003 MGI PMID:21499268 737425 Git1 GIT ArfGAP 1 gene MP:0001575 cyanosis IAGP N RGD:5509061 20141003 MGI PMID:19273721 737425 Git1 GIT ArfGAP 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:19273721 737425 Git1 GIT ArfGAP 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:17565117 737425 Git1 GIT ArfGAP 1 gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20141003 MGI PMID:21499268 737425 Git1 GIT ArfGAP 1 gene MP:0002803 abnormal operant conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:20043896 737425 Git1 GIT ArfGAP 1 gene MP:0003460 decreased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:19383529 737425 Git1 GIT ArfGAP 1 gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19273721 737425 Git1 GIT ArfGAP 1 gene MP:0004994 abnormal brain wave pattern IAGP N RGD:5509061 20141003 MGI PMID:21499268 737425 Git1 GIT ArfGAP 1 gene MP:0006057 decreased vascular endothelial cell number IAGP N RGD:5509061 20141003 MGI PMID:19273721 737425 Git1 GIT ArfGAP 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:20043896 737425 Git1 GIT ArfGAP 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19273721 737425 Git1 GIT ArfGAP 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:19383529 737425 Git1 GIT ArfGAP 1 gene MP:0008948 decreased neuron number IAGP N RGD:5509061 20141003 MGI PMID:21499268 737425 Git1 GIT ArfGAP 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19383529 737425 Git1 GIT ArfGAP 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19383529 737425 Git1 GIT ArfGAP 1 gene MP:0010856 dilated respiratory conducting tube IAGP N RGD:5509061 20141003 MGI PMID:19273721 737425 Git1 GIT ArfGAP 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19273721 737425 Git1 GIT ArfGAP 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21499268 737425 Git1 GIT ArfGAP 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19273721 737425 Git1 GIT ArfGAP 1 gene MP:0014383 decreased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:21499268 737425 Git1 GIT ArfGAP 1 gene MP:0020316 decreased vascular endothelial cell proliferation IAGP N RGD:5509061 20160616 MGI PMID:19273721 737425 Git1 GIT ArfGAP 1 gene MP:0020508 decreased dendritic spine density IAGP N RGD:5509061 20211014 MGI PMID:20043896 737431 Gsto1 glutathione S-transferase omega 1 gene MP:0001392 abnormal locomotor behavior IEA N RGD:5509061 20240523 MGI 737431 Gsto1 glutathione S-transferase omega 1 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20220811 MGI 737431 Gsto1 glutathione S-transferase omega 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20240523 MGI 737431 Gsto1 glutathione S-transferase omega 1 gene MP:0002075 abnormal coat/hair pigmentation IEA N RGD:5509061 20240523 MGI 737431 Gsto1 glutathione S-transferase omega 1 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 737431 Gsto1 glutathione S-transferase omega 1 gene MP:0005562 decreased mean corpuscular hemoglobin IEA N RGD:5509061 20220811 MGI 737431 Gsto1 glutathione S-transferase omega 1 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 737431 Gsto1 glutathione S-transferase omega 1 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 737433 Smcp sperm mitochondria-associated cysteine-rich protein gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:11940662 737433 Smcp sperm mitochondria-associated cysteine-rich protein gene MP:0000242 impaired fertilization IAGP N RGD:5509061 20141003 MGI PMID:15685642 737433 Smcp sperm mitochondria-associated cysteine-rich protein gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:15685642 737433 Smcp sperm mitochondria-associated cysteine-rich protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:11940662 737433 Smcp sperm mitochondria-associated cysteine-rich protein gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15685642 737433 Smcp sperm mitochondria-associated cysteine-rich protein gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11940662 737433 Smcp sperm mitochondria-associated cysteine-rich protein gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:15685642 737433 Smcp sperm mitochondria-associated cysteine-rich protein gene MP:0004542 impaired acrosome reaction IAGP N RGD:5509061 20141003 MGI PMID:11940662 737433 Smcp sperm mitochondria-associated cysteine-rich protein gene MP:0009230 abnormal sperm head morphology IAGP N RGD:5509061 20141003 MGI PMID:15685642 737433 Smcp sperm mitochondria-associated cysteine-rich protein gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20191226 MGI PMID:15685642 737433 Smcp sperm mitochondria-associated cysteine-rich protein gene MP:0030976 impaired sperm penetration of zona pellucida IAGP N RGD:5509061 20200102 MGI PMID:11940662 737433 Smcp sperm mitochondria-associated cysteine-rich protein gene MP:0030978 impaired binding of sperm to zona pellucida IAGP N RGD:5509061 20191017 MGI PMID:15685642 737433 Smcp sperm mitochondria-associated cysteine-rich protein gene MP:0031012 impaired sperm migration in female genital tract IAGP N RGD:5509061 20200227 MGI PMID:15685642 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000111 cleft palate IEA N RGD:5509061 20141003 MGI 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20211104 MGI PMID:34486668 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000286 abnormal mitral valve morphology IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000295 trabecula carnea hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000445 short snout IEA N RGD:5509061 20150402 MGI 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000531 right pulmonary isomerism IAGP N RGD:5509061 20141003 MGI PMID:19218456 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000534 abnormal ureter morphology IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000562 polydactyly IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000572 abnormal autopod morphology IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20141003 MGI PMID:19218456 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000644 dextrocardia IAGP N RGD:5509061 20211104 MGI PMID:34486668 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000650 mesocardia IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000650 mesocardia IAGP N RGD:5509061 20141003 MGI PMID:19218456 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000650 mesocardia IAGP N RGD:5509061 20211104 MGI PMID:34486668 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000690 absent spleen IAGP N RGD:5509061 20141003 MGI PMID:19218456 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20151203 MGI 737435 Megf8 multiple EGF-like-domains 8 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0001073 abnormal glossopharyngeal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0001074 abnormal vagus nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20410128 737435 Megf8 multiple EGF-like-domains 8 gene MP:0001077 abnormal spinal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0001265 decreased body size IEA N RGD:5509061 20151203 MGI 737435 Megf8 multiple EGF-like-domains 8 gene MP:0001293 anophthalmia IEA N RGD:5509061 20150402 MGI 737435 Megf8 multiple EGF-like-domains 8 gene MP:0001297 microphthalmia IEA N RGD:5509061 20151203 MGI 737435 Megf8 multiple EGF-like-domains 8 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0001823 thymus hypoplasia IEA N RGD:5509061 20151203 MGI 737435 Megf8 multiple EGF-like-domains 8 gene MP:0002624 abnormal tricuspid valve morphology IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20211104 MGI PMID:34486668 737435 Megf8 multiple EGF-like-domains 8 gene MP:0002639 micrognathia IEA N RGD:5509061 20150402 MGI 737435 Megf8 multiple EGF-like-domains 8 gene MP:0002745 abnormal atrioventricular valve morphology IAGP N RGD:5509061 20231228 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0002766 situs inversus IAGP N RGD:5509061 20211104 MGI PMID:34486668 737435 Megf8 multiple EGF-like-domains 8 gene MP:0003052 omphalocele IEA N RGD:5509061 20141003 MGI 737435 Megf8 multiple EGF-like-domains 8 gene MP:0003105 abnormal heart atrium morphology IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0003342 accessory spleen IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0003342 accessory spleen IAGP N RGD:5509061 20141003 MGI PMID:19218456 737435 Megf8 multiple EGF-like-domains 8 gene MP:0003446 renal hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0003632 abnormal nervous system morphology IAGP N RGD:5509061 20141003 MGI PMID:20410128 737435 Megf8 multiple EGF-like-domains 8 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0003921 abnormal heart left ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20141003 MGI PMID:19218456 737435 Megf8 multiple EGF-like-domains 8 gene MP:0004110 transposition of great arteries IAGP N RGD:5509061 20211104 MGI PMID:34486668 737435 Megf8 multiple EGF-like-domains 8 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20190725 MGI PMID:19218456 737435 Megf8 multiple EGF-like-domains 8 gene MP:0004133 heterotaxia IAGP N RGD:5509061 20211104 MGI PMID:34486668 737435 Megf8 multiple EGF-like-domains 8 gene MP:0004158 right aortic arch IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:19218456 737435 Megf8 multiple EGF-like-domains 8 gene MP:0004190 abnormal direction of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:19218456 737435 Megf8 multiple EGF-like-domains 8 gene MP:0004252 abnormal direction of heart looping IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0004320 split sternum IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0006061 right atrial isomerism IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0006065 abnormal heart position or orientation IAGP N RGD:5509061 20211104 MGI PMID:34486668 737435 Megf8 multiple EGF-like-domains 8 gene MP:0006113 abnormal heart septum morphology IAGP N RGD:5509061 20211104 MGI PMID:34486668 737435 Megf8 multiple EGF-like-domains 8 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:19218456 737435 Megf8 multiple EGF-like-domains 8 gene MP:0006126 abnormal cardiac outflow tract development IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0008816 petechiae IEA N RGD:5509061 20151203 MGI 737435 Megf8 multiple EGF-like-domains 8 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:20410128 737435 Megf8 multiple EGF-like-domains 8 gene MP:0009450 abnormal axon fasciculation IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0009743 preaxial polydactyly IAGP N RGD:5509061 20211104 MGI PMID:34486668 737435 Megf8 multiple EGF-like-domains 8 gene MP:0009798 abnormal ophthalmic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:20410128 737435 Megf8 multiple EGF-like-domains 8 gene MP:0009798 abnormal ophthalmic nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0009799 abnormal maxillary nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20211104 MGI PMID:34486668 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010403 atrial septal defect IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010412 atrioventricular septal defect IAGP N RGD:5509061 20211104 MGI PMID:34486668 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010413 complete atrioventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010420 muscular ventricular septal defect IEA N RGD:5509061 20141003 MGI 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010426 abnormal heart and great artery attachment IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010437 absent coronary sinus IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010440 anomalous pulmonary venous connection IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010440 anomalous pulmonary venous connection IAGP N RGD:5509061 20141003 MGI PMID:19218456 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010449 heart right ventricle outflow tract stenosis IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010476 coronary fistula IEA N RGD:5509061 20141003 MGI 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010807 abnormal stomach position or orientation IAGP N RGD:5509061 20141003 MGI PMID:18043505 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010808 right-sided stomach IAGP N RGD:5509061 20141003 MGI PMID:19218456 737435 Megf8 multiple EGF-like-domains 8 gene MP:0010854 lung situs inversus IAGP N RGD:5509061 20211104 MGI PMID:34486668 737435 Megf8 multiple EGF-like-domains 8 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0011665 d-loop transposition of the great arteries IEA N RGD:5509061 20141003 MGI 737435 Megf8 multiple EGF-like-domains 8 gene MP:0011666 double outlet right ventricle, ventricular defect committed to aorta IEA N RGD:5509061 20141003 MGI 737435 Megf8 multiple EGF-like-domains 8 gene MP:0011668 double outlet right ventricle, Taussig bing type IEA N RGD:5509061 20141003 MGI 737435 Megf8 multiple EGF-like-domains 8 gene MP:0012531 delayed limb development IAGP N RGD:5509061 20141003 MGI PMID:24052814 737435 Megf8 multiple EGF-like-domains 8 gene MP:0031284 abdominal situs abnormality IAGP N RGD:5509061 20211104 MGI PMID:34486668 737436 Dbn1 drebrin 1 gene MP:0000137 abnormal vertebrae morphology IEA N RGD:5509061 20201022 MGI 737436 Dbn1 drebrin 1 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20141003 MGI 737436 Dbn1 drebrin 1 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20141003 MGI 737436 Dbn1 drebrin 1 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20160804 MGI 737436 Dbn1 drebrin 1 gene MP:0000218 increased leukocyte cell number IEA N RGD:5509061 20211021 MGI 737436 Dbn1 drebrin 1 gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20230119 MGI 737436 Dbn1 drebrin 1 gene MP:0000274 enlarged heart IEA N RGD:5509061 20190502 MGI 737436 Dbn1 drebrin 1 gene MP:0000433 microcephaly IEA N RGD:5509061 20230601 MGI 737436 Dbn1 drebrin 1 gene MP:0000564 syndactyly IEA N RGD:5509061 20230601 MGI 737436 Dbn1 drebrin 1 gene MP:0000598 abnormal liver morphology IEA N RGD:5509061 20230119 MGI 737436 Dbn1 drebrin 1 gene MP:0000602 dilated liver sinusoidal space IEA N RGD:5509061 20170504 MGI 737436 Dbn1 drebrin 1 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 737436 Dbn1 drebrin 1 gene MP:0000787 abnormal telencephalon morphology IEA N RGD:5509061 20170504 MGI 737436 Dbn1 drebrin 1 gene MP:0000807 abnormal hippocampus morphology IAGP N RGD:5509061 20160811 MGI PMID:25865831 737436 Dbn1 drebrin 1 gene MP:0001262 decreased body weight IEA N RGD:5509061 20141003 MGI 737436 Dbn1 drebrin 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20211021 MGI 737436 Dbn1 drebrin 1 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20230119 MGI 737436 Dbn1 drebrin 1 gene MP:0001415 increased exploration in new environment IEA N RGD:5509061 20211021 MGI 737436 Dbn1 drebrin 1 gene MP:0001491 unresponsive to tactile stimuli IEA N RGD:5509061 20210520 MGI 737436 Dbn1 drebrin 1 gene MP:0001510 abnormal coat appearance IEA N RGD:5509061 20190502 MGI 737436 Dbn1 drebrin 1 gene MP:0001566 increased circulating phosphate level IEA N RGD:5509061 20160421 MGI 737436 Dbn1 drebrin 1 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20160811 MGI 737436 Dbn1 drebrin 1 gene MP:0001700 abnormal embryo turning IEA N RGD:5509061 20181227 MGI 737436 Dbn1 drebrin 1 gene MP:0001726 abnormal allantois morphology IEA N RGD:5509061 20181227 MGI 737436 Dbn1 drebrin 1 gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20160811 MGI PMID:25865831 737436 Dbn1 drebrin 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20141003 MGI 737436 Dbn1 drebrin 1 gene MP:0002702 decreased circulating free fatty acids level IEA N RGD:5509061 20201022 MGI 737436 Dbn1 drebrin 1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20211021 MGI 737436 Dbn1 drebrin 1 gene MP:0002824 abnormal chorioallantoic fusion IEA N RGD:5509061 20181227 MGI 737436 Dbn1 drebrin 1 gene MP:0002942 decreased circulating alanine transaminase level IEA N RGD:5509061 20141003 MGI 737436 Dbn1 drebrin 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 737436 Dbn1 drebrin 1 gene MP:0003019 increased circulating chloride level IEA N RGD:5509061 20141003 MGI 737436 Dbn1 drebrin 1 gene MP:0003960 increased lean body mass IEA N RGD:5509061 20150430 MGI 737436 Dbn1 drebrin 1 gene MP:0005179 decreased circulating cholesterol level IEA N RGD:5509061 20141003 MGI 737436 Dbn1 drebrin 1 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20141003 MGI 737436 Dbn1 drebrin 1 gene MP:0005553 increased circulating creatinine level IEA N RGD:5509061 20211021 MGI 737436 Dbn1 drebrin 1 gene MP:0005567 decreased circulating total protein level IEA N RGD:5509061 20141003 MGI 737436 Dbn1 drebrin 1 gene MP:0005632 decreased circulating aspartate transaminase level IEA N RGD:5509061 20141003 MGI 737436 Dbn1 drebrin 1 gene MP:0008026 abnormal brain white matter morphology IEA N RGD:5509061 20170504 MGI 737436 Dbn1 drebrin 1 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20201231 MGI 737436 Dbn1 drebrin 1 gene MP:0008128 abnormal brain internal capsule morphology IEA N RGD:5509061 20170504 MGI 737436 Dbn1 drebrin 1 gene MP:0008922 abnormal cervical rib IEA N RGD:5509061 20170504 MGI 737436 Dbn1 drebrin 1 gene MP:0008935 decreased mean platelet volume IEA N RGD:5509061 20210128 MGI 737436 Dbn1 drebrin 1 gene MP:0009141 increased prepulse inhibition IEA N RGD:5509061 20231207 MGI 737436 Dbn1 drebrin 1 gene MP:0009456 impaired cued conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19837137 737436 Dbn1 drebrin 1 gene MP:0009936 abnormal dendritic spine morphology IAGP N RGD:5509061 20160811 MGI PMID:25865831 737436 Dbn1 drebrin 1 gene MP:0010025 decreased total body fat amount IEA N RGD:5509061 20141003 MGI 737436 Dbn1 drebrin 1 gene MP:0010053 decreased grip strength IEA N RGD:5509061 20201022 MGI 737436 Dbn1 drebrin 1 gene MP:0010067 increased red blood cell distribution width IEA N RGD:5509061 20210520 MGI 737436 Dbn1 drebrin 1 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20141003 MGI 737436 Dbn1 drebrin 1 gene MP:0010092 increased circulating magnesium level IEA N RGD:5509061 20201022 MGI 737436 Dbn1 drebrin 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20201022 MGI 737436 Dbn1 drebrin 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20160421 MGI 737436 Dbn1 drebrin 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20150430 MGI 737436 Dbn1 drebrin 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20160421 MGI 737436 Dbn1 drebrin 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230119 MGI 737436 Dbn1 drebrin 1 gene MP:0013824 abnormal hypoglossal canal morphology IEA N RGD:5509061 20170504 MGI 737436 Dbn1 drebrin 1 gene MP:0013826 absent hypoglossal canal IEA N RGD:5509061 20170504 MGI 737436 Dbn1 drebrin 1 gene MP:0013834 thin hypoglossal nerve IEA N RGD:5509061 20170504 MGI 737436 Dbn1 drebrin 1 gene MP:0013835 absent hypoglossal nerve IEA N RGD:5509061 20170504 MGI 737436 Dbn1 drebrin 1 gene MP:0013915 abnormal brachial plexus formation IEA N RGD:5509061 20170504 MGI 737436 Dbn1 drebrin 1 gene MP:0014017 abnormal Wolffian duct connection IEA N RGD:5509061 20170504 MGI 737437 Vps33b vacuolar protein sorting 33B gene MP:0000219 increased neutrophil cell number IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0000414 alopecia IAGP N RGD:5509061 20170126 MGI PMID:27435297 737437 Vps33b vacuolar protein sorting 33B gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0001192 scaly skin IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0001192 scaly skin IAGP N RGD:5509061 20170126 MGI PMID:27435297 737437 Vps33b vacuolar protein sorting 33B gene MP:0001212 skin lesions IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20211021 MGI 737437 Vps33b vacuolar protein sorting 33B gene MP:0001711 abnormal placenta morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 737437 Vps33b vacuolar protein sorting 33B gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0003853 dry skin IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0003853 dry skin IAGP N RGD:5509061 20170126 MGI PMID:27435297 737437 Vps33b vacuolar protein sorting 33B gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0005031 abnormal trophoblast layer morphology IAGP N RGD:5509061 20190912 MGI PMID:29539633 737437 Vps33b vacuolar protein sorting 33B gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0008127 decreased dendritic cell number IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0008935 decreased mean platelet volume IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20160602 MGI PMID:25947942 737437 Vps33b vacuolar protein sorting 33B gene MP:0010099 abnormal thoracic cage shape IEA N RGD:5509061 20150430 MGI 737437 Vps33b vacuolar protein sorting 33B gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20190912 MGI PMID:29539633 737437 Vps33b vacuolar protein sorting 33B gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737437 Vps33b vacuolar protein sorting 33B gene MP:0011643 abnormal tendon collagen fibril morphology IAGP N RGD:5509061 20170126 MGI PMID:27435297 737437 Vps33b vacuolar protein sorting 33B gene MP:0020431 decreased platelet alpha-granule number IAGP N RGD:5509061 20170720 MGI PMID:25947942 737438 Ctbp1 C-terminal binding protein 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0001258 decreased body length IEA N RGD:5509061 20230601 MGI 737438 Ctbp1 C-terminal binding protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0001690 failure of somite differentiation IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0001701 incomplete embryo turning IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0002279 abnormal diaphragm morphology IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0003720 abnormal neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0005225 abnormal vertebrae development IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12101226 737438 Ctbp1 C-terminal binding protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 737438 Ctbp1 C-terminal binding protein 1 gene MP:0011732 decreased somite size IAGP N RGD:5509061 20141003 MGI PMID:12101226 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0000060 delayed bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0000160 kyphosis IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0000166 abnormal chondrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:10995453 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:10995453 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0002132 abnormal respiratory system morphology IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0002621 delayed neural tube closure IAGP N RGD:5509061 20141003 MGI PMID:10995453 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0002657 chondrodystrophy IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0002765 short fibula IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0002823 abnormal rib development IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0003419 delayed endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0003723 abnormal long bone morphology IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10995453 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0004351 short humerus IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0004355 short radius IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0004359 short ulna IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0004599 abnormal vertebral arch morphology IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0004624 abnormal thoracic cage morphology IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0004711 persistence of notochord tissue IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0005245 hemarthrosis IAGP N RGD:5509061 20181018 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0005296 abnormal humerus morphology IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0005306 abnormal phalanx morphology IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0008271 abnormal bone ossification IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0010988 abnormal bronchial cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:22492985 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10995453 737440 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1 gene MP:0013945 abnormal elbow joint morphology IAGP N RGD:5509061 20181018 MGI PMID:22492985 737442 Gng5 G protein subunit gamma 5 gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20151231 MGI PMID:24599258 737442 Gng5 G protein subunit gamma 5 gene MP:0000270 abnormal heart tube morphology IAGP N RGD:5509061 20151231 MGI PMID:24599258 737442 Gng5 G protein subunit gamma 5 gene MP:0003872 absent heart right ventricle IAGP N RGD:5509061 20151231 MGI PMID:24599258 737442 Gng5 G protein subunit gamma 5 gene MP:0003873 pharyngeal arch hypoplasia IAGP N RGD:5509061 20151231 MGI PMID:24599258 737442 Gng5 G protein subunit gamma 5 gene MP:0004251 failure of heart looping IAGP N RGD:5509061 20151231 MGI PMID:24599258 737442 Gng5 G protein subunit gamma 5 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20151231 MGI PMID:24599258 737442 Gng5 G protein subunit gamma 5 gene MP:0011257 abnormal head fold morphology IAGP N RGD:5509061 20151231 MGI PMID:24599258 737442 Gng5 G protein subunit gamma 5 gene MP:0011395 decreased fetal cardiomyocyte proliferation IAGP N RGD:5509061 20151231 MGI PMID:24599258 737442 Gng5 G protein subunit gamma 5 gene MP:0012278 abnormal cardiogenic mesoderm morphology IAGP N RGD:5509061 20151231 MGI PMID:24599258 737442 Gng5 G protein subunit gamma 5 gene MP:0012511 dilated aortic sac IAGP N RGD:5509061 20151231 MGI PMID:24599258 737442 Gng5 G protein subunit gamma 5 gene MP:0013267 first pharyngeal arch hypoplasia IAGP N RGD:5509061 20151231 MGI PMID:24599258 737442 Gng5 G protein subunit gamma 5 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20151231 MGI PMID:24599258 737442 Gng5 G protein subunit gamma 5 gene MP:0014044 absent cardiac outflow tract IAGP N RGD:5509061 20160304 MGI PMID:24599258 737443 Gap43 growth associated protein 43 gene MP:0000788 abnormal cerebral cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:10430954 737443 Gap43 growth associated protein 43 gene MP:0000861 disorganized barrel cortex IAGP N RGD:5509061 20141003 MGI PMID:10430954 737443 Gap43 growth associated protein 43 gene MP:0001260 increased body weight IEA N RGD:5509061 20160804 MGI 737443 Gap43 growth associated protein 43 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:7859286 737443 Gap43 growth associated protein 43 gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:7859286 737443 Gap43 growth associated protein 43 gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:9671660 737443 Gap43 growth associated protein 43 gene MP:0001332 abnormal optic nerve innervation IAGP N RGD:5509061 20141003 MGI PMID:9852588 737443 Gap43 growth associated protein 43 gene MP:0001334 absent optic tract IAGP N RGD:5509061 20141003 MGI PMID:9671660 737443 Gap43 growth associated protein 43 gene MP:0001334 absent optic tract IAGP N RGD:5509061 20141003 MGI PMID:9852588 737443 Gap43 growth associated protein 43 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7859286 737443 Gap43 growth associated protein 43 gene MP:0002961 abnormal axon guidance IAGP N RGD:5509061 20141003 MGI PMID:10430954 737443 Gap43 growth associated protein 43 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:10430954 737443 Gap43 growth associated protein 43 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:11161469 737443 Gap43 growth associated protein 43 gene MP:0005404 abnormal axon morphology IAGP N RGD:5509061 20141003 MGI PMID:9852588 737443 Gap43 growth associated protein 43 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:10430954 737443 Gap43 growth associated protein 43 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10430954 737443 Gap43 growth associated protein 43 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:10430954 737443 Gap43 growth associated protein 43 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7859286 737443 Gap43 growth associated protein 43 gene MP:0020549 increased optic chiasm size IAGP N RGD:5509061 20180301 MGI PMID:7859286 737444 Gabrg1 gamma-aminobutyric acid type A receptor subunit gamma 1 gene MP:0020374 abnormal nocifensive behavior IAGP N RGD:5509061 20210304 MGI PMID:33083721 737444 Gabrg1 gamma-aminobutyric acid type A receptor subunit gamma 1 gene MP:0020954 decreased mechanical nociceptive threshold IAGP N RGD:5509061 20210304 MGI PMID:33083721 737445 Gk glycerol kinase gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:16105550 737445 Gk glycerol kinase gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20141003 MGI PMID:9302256 737445 Gk glycerol kinase gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:16105550 737445 Gk glycerol kinase gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:16105550 737445 Gk glycerol kinase gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:9302256 737445 Gk glycerol kinase gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9302256 737445 Gk glycerol kinase gene MP:0001746 abnormal pituitary secretion IAGP N RGD:5509061 20141003 MGI PMID:9302256 737445 Gk glycerol kinase gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:9302256 737445 Gk glycerol kinase gene MP:0003443 increased circulating glycerol level IAGP N RGD:5509061 20141003 MGI PMID:9302256 737445 Gk glycerol kinase gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:9302256 737445 Gk glycerol kinase gene MP:0005282 decreased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:19270708 737445 Gk glycerol kinase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:19270708 737445 Gk glycerol kinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16105550 737445 Gk glycerol kinase gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9302256 737445 Gk glycerol kinase gene MP:0030780 increased urine glycerol level IAGP N RGD:5509061 20181004 MGI PMID:9302256 737447 Arpp19 cAMP-regulated phosphoprotein 19 gene MP:0001672 abnormal embryo development IAGP N RGD:5509061 20191205 MGI PMID:30626720 737447 Arpp19 cAMP-regulated phosphoprotein 19 gene MP:0001696 failure to gastrulate IAGP N RGD:5509061 20191205 MGI PMID:30626720 737447 Arpp19 cAMP-regulated phosphoprotein 19 gene MP:0001730 embryonic growth arrest IAGP N RGD:5509061 20191205 MGI PMID:30626720 737447 Arpp19 cAMP-regulated phosphoprotein 19 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20191205 MGI PMID:30626720 737447 Arpp19 cAMP-regulated phosphoprotein 19 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20191205 MGI PMID:30626720 737448 Cat catalase gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:4713148 737448 Cat catalase gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:5087482 737448 Cat catalase gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20141003 MGI PMID:6058079 737448 Cat catalase gene MP:0004499 increased incidence of tumors by chemical induction IAGP N RGD:5509061 20141003 MGI PMID:642030 737448 Cat catalase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:4713148 737448 Cat catalase gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:5087482 737448 Cat catalase gene MP:0009767 decreased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:642030 737448 Cat catalase gene MP:0010264 increased hepatoma incidence IEA N RGD:5509061 20111116 MGI 737448 Cat catalase gene MP:0010269 decreased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:642030 737448 Cat catalase gene MP:0010957 abnormal aerobic respiration IAGP N RGD:5509061 20141003 MGI PMID:15178682 737448 Cat catalase gene MP:0011592 abnormal catalase activity IAGP N RGD:5509061 20141003 MGI PMID:5929246 737448 Cat catalase gene MP:0011592 abnormal catalase activity IAGP N RGD:5509061 20141003 MGI PMID:6058079 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0000183 decreased circulating LDL cholesterol level IEA N RGD:5509061 20141003 MGI 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0000186 decreased circulating HDL cholesterol level IEA N RGD:5509061 20160804 MGI 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0002968 increased circulating alkaline phosphatase level IAGP N RGD:5509061 20141003 MGI PMID:16709608 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0005135 increased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:16709608 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:16709608 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:16709608 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:16709608 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0005469 abnormal thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:17318265 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0005472 abnormal triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:17318265 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0005473 decreased triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:16709608 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0005474 increased triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:16709608 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0005476 abnormal circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:16709608 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:16709608 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:17318265 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:17318265 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0005554 decreased circulating creatinine level IEA N RGD:5509061 20160804 MGI 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:16709608 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20160804 MGI 737452 Slc16a2 solute carrier family 16 (monocarboxylic acid transporters), member 2 gene MP:0010088 decreased circulating fructosamine level IEA N RGD:5509061 20160804 MGI 737454 Adnp activity-dependent neuroprotective protein gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:12888219 737454 Adnp activity-dependent neuroprotective protein gene MP:0002085 abnormal embryonic tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:12888219 737454 Adnp activity-dependent neuroprotective protein gene MP:0011097 embryonic lethality between somite formation and embryo turning, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12888219 737456 Mylk2 myosin, light polypeptide kinase 2, skeletal muscle gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:16299103 737458 Il7 interleukin 7 gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17179092 737458 Il7 interleukin 7 gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20141003 MGI PMID:9486111 737458 Il7 interleukin 7 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:17179092 737458 Il7 interleukin 7 gene MP:0000692 small spleen IAGP N RGD:5509061 20141003 MGI PMID:7699333 737458 Il7 interleukin 7 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17151827 737458 Il7 interleukin 7 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17179092 737458 Il7 interleukin 7 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7699333 737458 Il7 interleukin 7 gene MP:0000694 spleen hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9486111 737458 Il7 interleukin 7 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:17179092 737458 Il7 interleukin 7 gene MP:0000706 small thymus IAGP N RGD:5509061 20141003 MGI PMID:7699333 737458 Il7 interleukin 7 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:11034372 737458 Il7 interleukin 7 gene MP:0000715 decreased thymocyte number IAGP N RGD:5509061 20141003 MGI PMID:23657000 737458 Il7 interleukin 7 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23657000 737458 Il7 interleukin 7 gene MP:0001802 arrested B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7699333 737458 Il7 interleukin 7 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17151827 737458 Il7 interleukin 7 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17179092 737458 Il7 interleukin 7 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:23657000 737458 Il7 interleukin 7 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:7699333 737458 Il7 interleukin 7 gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9486111 737458 Il7 interleukin 7 gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:23018454 737458 Il7 interleukin 7 gene MP:0002217 small lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:23657000 737458 Il7 interleukin 7 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:17179092 737458 Il7 interleukin 7 gene MP:0002831 absent Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:7699333 737458 Il7 interleukin 7 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:17179092 737458 Il7 interleukin 7 gene MP:0004953 decreased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:7699333 737458 Il7 interleukin 7 gene MP:0004956 decreased thymus weight IAGP N RGD:5509061 20141003 MGI PMID:7699333 737458 Il7 interleukin 7 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17873878 737458 Il7 interleukin 7 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:23018454 737458 Il7 interleukin 7 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:7699333 737458 Il7 interleukin 7 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:17151827 737458 Il7 interleukin 7 gene MP:0005017 decreased B cell number IAGP N RGD:5509061 20141003 MGI PMID:23018454 737458 Il7 interleukin 7 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:17179092 737458 Il7 interleukin 7 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23018454 737458 Il7 interleukin 7 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:23657000 737458 Il7 interleukin 7 gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:23018454 737458 Il7 interleukin 7 gene MP:0005232 abnormal mesenteric lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:23657000 737458 Il7 interleukin 7 gene MP:0008024 absent lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7699333 737458 Il7 interleukin 7 gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:23018454 737458 Il7 interleukin 7 gene MP:0008042 abnormal NK T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:23018454 737458 Il7 interleukin 7 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20141003 MGI PMID:12586624 737458 Il7 interleukin 7 gene MP:0008083 decreased single-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:17151827 737458 Il7 interleukin 7 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:17151827 737458 Il7 interleukin 7 gene MP:0008250 abnormal myeloid leukocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:17151827 737458 Il7 interleukin 7 gene MP:0008465 absent mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17179092 737458 Il7 interleukin 7 gene MP:0009624 small inguinal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17179092 737458 Il7 interleukin 7 gene MP:0009630 absent axillary lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17179092 737458 Il7 interleukin 7 gene MP:0009633 absent cervical lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17179092 737458 Il7 interleukin 7 gene MP:0009634 absent popliteal lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:17179092 737463 Txn2 thioredoxin 2 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:12529397 737463 Txn2 thioredoxin 2 gene MP:0000928 incomplete rostral neuropore closure IAGP N RGD:5509061 20141003 MGI PMID:12529397 737463 Txn2 thioredoxin 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20141003 MGI PMID:12529397 737463 Txn2 thioredoxin 2 gene MP:0010954 abnormal cellular respiration IAGP N RGD:5509061 20141003 MGI PMID:12529397 737463 Txn2 thioredoxin 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12529397 737463 Txn2 thioredoxin 2 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:12529397 737464 Abcc5 ATP-binding cassette, sub-family C member 5 gene MP:0000195 decreased circulating calcium level IEA N RGD:5509061 20211021 MGI 737464 Abcc5 ATP-binding cassette, sub-family C member 5 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20181227 MGI 737464 Abcc5 ATP-binding cassette, sub-family C member 5 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210520 MGI 737464 Abcc5 ATP-binding cassette, sub-family C member 5 gene MP:0001513 limb grasping IEA N RGD:5509061 20181227 MGI 737464 Abcc5 ATP-binding cassette, sub-family C member 5 gene MP:0005012 decreased eosinophil cell number IEA N RGD:5509061 20181227 MGI 737464 Abcc5 ATP-binding cassette, sub-family C member 5 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20181227 MGI 737464 Abcc5 ATP-binding cassette, sub-family C member 5 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20210128 MGI 737464 Abcc5 ATP-binding cassette, sub-family C member 5 gene MP:0005560 decreased circulating glucose level IEA N RGD:5509061 20181227 MGI 737464 Abcc5 ATP-binding cassette, sub-family C member 5 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:10453003 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:11035773 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:10453003 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0000703 abnormal thymus morphology IAGP N RGD:5509061 20141003 MGI PMID:9256476 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20141003 MGI PMID:10411922 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0001844 autoimmune response IAGP N RGD:5509061 20141003 MGI PMID:19188497 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0001856 myocarditis IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0001864 vascular inflammation IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0001869 pancreas inflammation IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10411922 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10453003 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11035773 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16882704 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9256476 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002145 abnormal T cell differentiation IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16037385 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20141003 MGI PMID:10411922 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10453003 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11239447 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19188497 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0002933 joint inflammation IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:10453003 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:11239447 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0003944 abnormal T cell subpopulation ratio IAGP N RGD:5509061 20141003 MGI PMID:10411922 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0004031 insulitis IAGP N RGD:5509061 20141003 MGI PMID:11035773 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0004751 increased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:11285307 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0004946 abnormal regulatory T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19188497 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0004973 increased regulatory T cell number IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0005010 abnormal CD8-positive, alpha beta T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:17873878 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0005018 decreased T cell number IAGP N RGD:5509061 20141003 MGI PMID:9256476 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:11035773 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0005090 increased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:9256476 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0005092 decreased double-positive T cell number IAGP N RGD:5509061 20141003 MGI PMID:9256476 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0005095 decreased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:11285307 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10411922 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:10453003 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0005348 increased T cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:17873878 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008037 abnormal T cell morphology IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10411922 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16882704 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008075 decreased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:11285307 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:10411922 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008079 decreased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:16882704 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008101 lymph node hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9256476 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008102 lymph node hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:16882704 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008568 abnormal interleukin secretion IAGP N RGD:5509061 20141003 MGI PMID:11285307 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:10411922 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008750 abnormal interferon level IAGP N RGD:5509061 20141003 MGI PMID:11285307 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:18845758 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008826 abnormal splenic cell ratio IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:7584144 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0009333 abnormal splenocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:11035773 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0010016 variable depigmentation IAGP N RGD:5509061 20141003 MGI PMID:16882704 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 737466 Ctla4 cytotoxic T-lymphocyte-associated protein 4 gene MP:0013435 decreased CD8-positive, naive alpha-beta T cell number IEA N RGD:5509061 20181011 MGI 737475 Rnase1 ribonuclease, RNase A family, 1 (pancreatic) gene MP:0001260 increased body weight IAGP N RGD:5509061 20201001 MGI PMID:31053653 737475 Rnase1 ribonuclease, RNase A family, 1 (pancreatic) gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20181227 MGI 737475 Rnase1 ribonuclease, RNase A family, 1 (pancreatic) gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20201001 MGI PMID:31053653 737475 Rnase1 ribonuclease, RNase A family, 1 (pancreatic) gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20201001 MGI PMID:31053653 737475 Rnase1 ribonuclease, RNase A family, 1 (pancreatic) gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 737475 Rnase1 ribonuclease, RNase A family, 1 (pancreatic) gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20201001 MGI PMID:31053653 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0000188 abnormal circulating glucose level IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0000189 hypoglycemia IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0001394 circling IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0002712 increased circulating glucagon level IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0003339 decreased pancreatic beta cell number IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0003402 decreased liver weight IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0005191 head tilt IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0009146 abnormal pancreatic acinar cell morphology IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0009160 abnormal pancreatic acinar cell zymogen granule morphology IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0009176 increased pancreatic alpha cell number IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0009378 abnormal endoplasmic reticulum morphology IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0012556 increased cell death IAGP N RGD:5509061 20151231 MGI PMID:24336520 737477 Dnajb9 DnaJ heat shock protein family (Hsp40) member B9 gene MP:0014117 increased pancreatic beta cell apoptosis IAGP N RGD:5509061 20161229 MGI PMID:24336520 737479 Rnf4 ring finger protein 4 gene MP:0001146 abnormal testis morphology IEA N RGD:5509061 20200514 MGI 737479 Rnf4 ring finger protein 4 gene MP:0001147 small testis IEA N RGD:5509061 20200514 MGI 737479 Rnf4 ring finger protein 4 gene MP:0001404 no spontaneous movement IEA N RGD:5509061 20210520 MGI 737479 Rnf4 ring finger protein 4 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:20696907 737479 Rnf4 ring finger protein 4 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 737479 Rnf4 ring finger protein 4 gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20210128 MGI 737479 Rnf4 ring finger protein 4 gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20210520 MGI 737479 Rnf4 ring finger protein 4 gene MP:0008877 abnormal DNA methylation IAGP N RGD:5509061 20141003 MGI PMID:20696907 737479 Rnf4 ring finger protein 4 gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:20696907 737479 Rnf4 ring finger protein 4 gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20696907 737479 Rnf4 ring finger protein 4 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201022 MGI 737483 Itgb3 integrin beta 3 gene MP:0000062 increased bone mineral density IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0000067 osteopetrosis IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0000195 decreased circulating calcium level IAGP N RGD:5509061 20141003 MGI PMID:10683372 737483 Itgb3 integrin beta 3 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:17627302 737483 Itgb3 integrin beta 3 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17184791 737483 Itgb3 integrin beta 3 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:17627302 737483 Itgb3 integrin beta 3 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0000465 gastrointestinal hemorrhage IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0001194 dermatitis IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:24107997 737483 Itgb3 integrin beta 3 gene MP:0001245 thick dermal layer IAGP N RGD:5509061 20141003 MGI PMID:24107997 737483 Itgb3 integrin beta 3 gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:10683372 737483 Itgb3 integrin beta 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:12746502 737483 Itgb3 integrin beta 3 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0001625 cardiac hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17184791 737483 Itgb3 integrin beta 3 gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12746502 737483 Itgb3 integrin beta 3 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0001915 intracranial hemorrhage IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12746502 737483 Itgb3 integrin beta 3 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0002166 abnormal tumor susceptibility IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19005179 737483 Itgb3 integrin beta 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:17184791 737483 Itgb3 integrin beta 3 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20141003 MGI PMID:16317099 737483 Itgb3 integrin beta 3 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20141003 MGI PMID:10548108 737483 Itgb3 integrin beta 3 gene MP:0002551 abnormal blood coagulation IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0002590 increased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:17627302 737483 Itgb3 integrin beta 3 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:17184791 737483 Itgb3 integrin beta 3 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0002724 enhanced wound healing IAGP N RGD:5509061 20141003 MGI PMID:15654327 737483 Itgb3 integrin beta 3 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:17184791 737483 Itgb3 integrin beta 3 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:17627302 737483 Itgb3 integrin beta 3 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:17627302 737483 Itgb3 integrin beta 3 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0003091 abnormal cell migration IAGP N RGD:5509061 20141003 MGI PMID:11786903 737483 Itgb3 integrin beta 3 gene MP:0003566 abnormal cell adhesion IAGP N RGD:5509061 20141003 MGI PMID:11786903 737483 Itgb3 integrin beta 3 gene MP:0003710 abnormal physiological neovascularization IAGP N RGD:5509061 20141003 MGI PMID:15654327 737483 Itgb3 integrin beta 3 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:16317099 737483 Itgb3 integrin beta 3 gene MP:0003721 increased tumor growth/size IAGP N RGD:5509061 20141003 MGI PMID:11786903 737483 Itgb3 integrin beta 3 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:17184791 737483 Itgb3 integrin beta 3 gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:17184791 737483 Itgb3 integrin beta 3 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:17184791 737483 Itgb3 integrin beta 3 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20141003 MGI PMID:15654327 737483 Itgb3 integrin beta 3 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:17184791 737483 Itgb3 integrin beta 3 gene MP:0003946 renal necrosis IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0004014 abnormal uterine environment IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:17184791 737483 Itgb3 integrin beta 3 gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:10683372 737483 Itgb3 integrin beta 3 gene MP:0004266 pale placenta IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0004485 increased response of heart to induced stress IAGP N RGD:5509061 20141003 MGI PMID:17184791 737483 Itgb3 integrin beta 3 gene MP:0004510 myositis IAGP N RGD:5509061 20141003 MGI PMID:17184791 737483 Itgb3 integrin beta 3 gene MP:0004898 uterine hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20141003 MGI PMID:10683372 737483 Itgb3 integrin beta 3 gene MP:0004982 abnormal osteoclast morphology IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:10683372 737483 Itgb3 integrin beta 3 gene MP:0004985 decreased osteoclast cell number IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0005048 abnormal thrombosis IAGP N RGD:5509061 20141003 MGI PMID:18086863 737483 Itgb3 integrin beta 3 gene MP:0005140 decreased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:17184791 737483 Itgb3 integrin beta 3 gene MP:0005179 decreased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12746502 737483 Itgb3 integrin beta 3 gene MP:0005333 decreased heart rate IAGP N RGD:5509061 20141003 MGI PMID:17184791 737483 Itgb3 integrin beta 3 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:12746502 737483 Itgb3 integrin beta 3 gene MP:0005422 osteosclerosis IAGP N RGD:5509061 20141003 MGI PMID:10683372 737483 Itgb3 integrin beta 3 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:15654327 737483 Itgb3 integrin beta 3 gene MP:0005464 abnormal platelet physiology IAGP N RGD:5509061 20141003 MGI PMID:19005179 737483 Itgb3 integrin beta 3 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12746502 737483 Itgb3 integrin beta 3 gene MP:0005561 increased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:17627302 737483 Itgb3 integrin beta 3 gene MP:0005601 increased angiogenesis IAGP N RGD:5509061 20141003 MGI PMID:11786903 737483 Itgb3 integrin beta 3 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:17627302 737483 Itgb3 integrin beta 3 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:19005179 737483 Itgb3 integrin beta 3 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0005606 increased bleeding time IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:12746502 737483 Itgb3 integrin beta 3 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:17627302 737483 Itgb3 integrin beta 3 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:19005179 737483 Itgb3 integrin beta 3 gene MP:0006298 abnormal platelet activation IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0008028 pregnancy-related premature death IAGP N RGD:5509061 20141003 MGI PMID:16317099 737483 Itgb3 integrin beta 3 gene MP:0008396 abnormal osteoclast differentiation IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0008438 abnormal cutaneous collagen fibril morphology IAGP N RGD:5509061 20141003 MGI PMID:24107997 737483 Itgb3 integrin beta 3 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:12746502 737483 Itgb3 integrin beta 3 gene MP:0008816 petechiae IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0008837 increased transforming growth factor beta level IAGP N RGD:5509061 20141003 MGI PMID:15654327 737483 Itgb3 integrin beta 3 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:10683372 737483 Itgb3 integrin beta 3 gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:20564195 737483 Itgb3 integrin beta 3 gene MP:0009446 abnormal platelet dense granule physiology IAGP N RGD:5509061 20141003 MGI PMID:19005179 737483 Itgb3 integrin beta 3 gene MP:0009549 decreased platelet aggregation IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0009584 decreased keratinocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:15654327 737483 Itgb3 integrin beta 3 gene MP:0009660 abnormal induced retina neovascularization IAGP N RGD:5509061 20141003 MGI PMID:11786903 737483 Itgb3 integrin beta 3 gene MP:0009676 abnormal hemostasis IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:12746502 737483 Itgb3 integrin beta 3 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20141003 MGI PMID:11786903 737483 Itgb3 integrin beta 3 gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0010878 increased trabecular bone volume IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12746502 737483 Itgb3 integrin beta 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17627302 737483 Itgb3 integrin beta 3 gene MP:0011514 skin hemorrhage IAGP N RGD:5509061 20201015 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0011515 purpura IAGP N RGD:5509061 20141003 MGI PMID:9916135 737483 Itgb3 integrin beta 3 gene MP:0020254 decreased collagen level IAGP N RGD:5509061 20151015 MGI PMID:19933310 737483 Itgb3 integrin beta 3 gene MP:0031120 decreased susceptibility to induced thrombosis IAGP N RGD:5509061 20201001 MGI PMID:19005179 737483 Itgb3 integrin beta 3 gene MP:0031434 increased miscarriage rate IAGP N RGD:5509061 20220915 MGI PMID:16317099 737483 Itgb3 integrin beta 3 gene MP:0031434 increased miscarriage rate IAGP N RGD:5509061 20220915 MGI PMID:9916135 737485 Adcy10 adenylate cyclase 10 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:14976244 737485 Adcy10 adenylate cyclase 10 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:16054031 737485 Adcy10 adenylate cyclase 10 gene MP:0001925 male infertility IAGP N RGD:5509061 20160714 MGI PMID:23611875 737485 Adcy10 adenylate cyclase 10 gene MP:0002626 increased heart rate IEA N RGD:5509061 20111116 MGI 737485 Adcy10 adenylate cyclase 10 gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:16054031 737485 Adcy10 adenylate cyclase 10 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:14976244 737485 Adcy10 adenylate cyclase 10 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16054031 737485 Adcy10 adenylate cyclase 10 gene MP:0003666 impaired sperm capacitation IAGP N RGD:5509061 20141003 MGI PMID:16054031 737485 Adcy10 adenylate cyclase 10 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20111116 MGI 737485 Adcy10 adenylate cyclase 10 gene MP:0005317 increased triglyceride level IEA N RGD:5509061 20111116 MGI 737485 Adcy10 adenylate cyclase 10 gene MP:0005410 abnormal fertilization IAGP N RGD:5509061 20141003 MGI PMID:14976244 737485 Adcy10 adenylate cyclase 10 gene MP:0005410 abnormal fertilization IAGP N RGD:5509061 20141003 MGI PMID:16054031 737485 Adcy10 adenylate cyclase 10 gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:16054031 737485 Adcy10 adenylate cyclase 10 gene MP:0009237 kinked sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:16054031 737485 Adcy10 adenylate cyclase 10 gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:16054031 737488 Ifng interferon gamma gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9531602 737488 Ifng interferon gamma gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9647244 737488 Ifng interferon gamma gene MP:0000220 increased monocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9531602 737488 Ifng interferon gamma gene MP:0000221 decreased leukocyte cell number IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:9531602 737488 Ifng interferon gamma gene MP:0000245 abnormal erythropoiesis IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20141003 MGI PMID:9531602 737488 Ifng interferon gamma gene MP:0000333 decreased bone marrow cell number IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20200611 MGI PMID:9765476 737488 Ifng interferon gamma gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9531602 737488 Ifng interferon gamma gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:9653090 737488 Ifng interferon gamma gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:9531602 737488 Ifng interferon gamma gene MP:0000701 abnormal lymph node size IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0000702 enlarged lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0001175 abnormal lung morphology IEA N RGD:5509061 20190502 MGI 737488 Ifng interferon gamma gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:19139386 737488 Ifng interferon gamma gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11342667 737488 Ifng interferon gamma gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:19734231 737488 Ifng interferon gamma gene MP:0001413 abnormal response to new environment IAGP N RGD:5509061 20141003 MGI PMID:10080860 737488 Ifng interferon gamma gene MP:0001577 anemia IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0001606 impaired hematopoiesis IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:9233639 737488 Ifng interferon gamma gene MP:0001656 focal hepatic necrosis IAGP N RGD:5509061 20200611 MGI PMID:11864749 737488 Ifng interferon gamma gene MP:0001793 abnormal susceptibility to infection IAGP N RGD:5509061 20141003 MGI PMID:9094668 737488 Ifng interferon gamma gene MP:0001800 abnormal humoral immune response IAGP N RGD:5509061 20141003 MGI PMID:9469425 737488 Ifng interferon gamma gene MP:0001805 decreased IgG level IAGP N RGD:5509061 20141003 MGI PMID:9647229 737488 Ifng interferon gamma gene MP:0001806 decreased IgM level IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0001807 decreased IgA level IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0001828 abnormal T cell activation IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9653090 737488 Ifng interferon gamma gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:12732663 737488 Ifng interferon gamma gene MP:0001847 brain inflammation IAGP N RGD:5509061 20141003 MGI PMID:23219391 737488 Ifng interferon gamma gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20141003 MGI PMID:12097414 737488 Ifng interferon gamma gene MP:0001860 liver inflammation IAGP N RGD:5509061 20141003 MGI PMID:11342667 737488 Ifng interferon gamma gene MP:0001860 liver inflammation IAGP N RGD:5509061 20200611 MGI PMID:9765476 737488 Ifng interferon gamma gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:12097414 737488 Ifng interferon gamma gene MP:0001861 lung inflammation IAGP N RGD:5509061 20141003 MGI PMID:9647244 737488 Ifng interferon gamma gene MP:0001861 lung inflammation IAGP N RGD:5509061 20151015 MGI PMID:17400729 737488 Ifng interferon gamma gene MP:0001873 stomach inflammation IAGP N RGD:5509061 20141003 MGI PMID:10878379 737488 Ifng interferon gamma gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:14978106 737488 Ifng interferon gamma gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9233639 737488 Ifng interferon gamma gene MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:9806748 737488 Ifng interferon gamma gene MP:0001882 abnormal lactation IAGP N RGD:5509061 20141003 MGI PMID:11445538 737488 Ifng interferon gamma gene MP:0001884 mammary gland alveolar hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11445538 737488 Ifng interferon gamma gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:10411532 737488 Ifng interferon gamma gene MP:0001942 abnormal lung volume IAGP N RGD:5509061 20151015 MGI PMID:17400729 737488 Ifng interferon gamma gene MP:0001952 increased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:9806748 737488 Ifng interferon gamma gene MP:0001958 emphysema IAGP N RGD:5509061 20151015 MGI PMID:17400729 737488 Ifng interferon gamma gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12093877 737488 Ifng interferon gamma gene MP:0002023 increased B cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12732663 737488 Ifng interferon gamma gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12093877 737488 Ifng interferon gamma gene MP:0002027 increased lung adenocarcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12093877 737488 Ifng interferon gamma gene MP:0002032 increased sarcoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12093877 737488 Ifng interferon gamma gene MP:0002038 increased carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12732663 737488 Ifng interferon gamma gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17483299 737488 Ifng interferon gamma gene MP:0002052 decreased tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18354038 737488 Ifng interferon gamma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:10490099 737488 Ifng interferon gamma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:11342667 737488 Ifng interferon gamma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12093877 737488 Ifng interferon gamma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12097414 737488 Ifng interferon gamma gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12732663 737488 Ifng interferon gamma gene MP:0002144 abnormal B cell differentiation IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18322463 737488 Ifng interferon gamma gene MP:0002224 abnormal spleen size IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20151015 MGI PMID:17400729 737488 Ifng interferon gamma gene MP:0002335 decreased airway responsiveness IAGP N RGD:5509061 20141003 MGI PMID:9806748 737488 Ifng interferon gamma gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0002343 abnormal lymph node cortex morphology IAGP N RGD:5509061 20141003 MGI PMID:9647244 737488 Ifng interferon gamma gene MP:0002345 abnormal lymph node primary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9647244 737488 Ifng interferon gamma gene MP:0002346 abnormal lymph node secondary follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9647244 737488 Ifng interferon gamma gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:9531602 737488 Ifng interferon gamma gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:9531602 737488 Ifng interferon gamma gene MP:0002376 abnormal dendritic cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16818748 737488 Ifng interferon gamma gene MP:0002398 abnormal bone marrow cell morphology/development IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:7504064 737488 Ifng interferon gamma gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8245795 737488 Ifng interferon gamma gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:8456300 737488 Ifng interferon gamma gene MP:0002412 increased susceptibility to bacterial infection IAGP N RGD:5509061 20141003 MGI PMID:9531602 737488 Ifng interferon gamma gene MP:0002416 abnormal proerythroblast morphology IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0002420 abnormal adaptive immunity IAGP N RGD:5509061 20141003 MGI PMID:9653090 737488 Ifng interferon gamma gene MP:0002425 abnormal susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:8635658 737488 Ifng interferon gamma gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:8456300 737488 Ifng interferon gamma gene MP:0002451 abnormal macrophage physiology IAGP N RGD:5509061 20141003 MGI PMID:9653090 737488 Ifng interferon gamma gene MP:0002455 abnormal dendritic cell antigen presentation IAGP N RGD:5509061 20141003 MGI PMID:16818748 737488 Ifng interferon gamma gene MP:0002459 abnormal B cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11067886 737488 Ifng interferon gamma gene MP:0002460 decreased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0002461 increased immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:12732663 737488 Ifng interferon gamma gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:7561104 737488 Ifng interferon gamma gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:7908325 737488 Ifng interferon gamma gene MP:0002490 abnormal immunoglobulin level IAGP N RGD:5509061 20141003 MGI PMID:9469425 737488 Ifng interferon gamma gene MP:0002492 decreased IgE level IAGP N RGD:5509061 20141003 MGI PMID:9806748 737488 Ifng interferon gamma gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:12732663 737488 Ifng interferon gamma gene MP:0002497 increased IgE level IAGP N RGD:5509061 20141003 MGI PMID:7908325 737488 Ifng interferon gamma gene MP:0002534 abnormal type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10383743 737488 Ifng interferon gamma gene MP:0002534 abnormal type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:9469425 737488 Ifng interferon gamma gene MP:0002608 increased hematocrit IEA N RGD:5509061 20200402 MGI 737488 Ifng interferon gamma gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:10438967 737488 Ifng interferon gamma gene MP:0002743 glomerulonephritis IAGP N RGD:5509061 20141003 MGI PMID:12097414 737488 Ifng interferon gamma gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:10080860 737488 Ifng interferon gamma gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:10438967 737488 Ifng interferon gamma gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20141003 MGI PMID:11342667 737488 Ifng interferon gamma gene MP:0002941 increased circulating alanine transaminase level IAGP N RGD:5509061 20200611 MGI PMID:11864749 737488 Ifng interferon gamma gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:10878379 737488 Ifng interferon gamma gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:7908325 737488 Ifng interferon gamma gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:8892638 737488 Ifng interferon gamma gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:9653090 737488 Ifng interferon gamma gene MP:0003179 thrombocytopenia IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0003186 abnormal redox activity IAGP N RGD:5509061 20141003 MGI PMID:17475277 737488 Ifng interferon gamma gene MP:0003257 abnormal abdominal wall morphology IAGP N RGD:5509061 20200611 MGI PMID:9765476 737488 Ifng interferon gamma gene MP:0003303 peritoneal inflammation IAGP N RGD:5509061 20200611 MGI PMID:9765476 737488 Ifng interferon gamma gene MP:0003306 small intestinal inflammation IAGP N RGD:5509061 20141003 MGI PMID:12486099 737488 Ifng interferon gamma gene MP:0003448 abnormal tumor morphology IAGP N RGD:5509061 20141003 MGI PMID:12093877 737488 Ifng interferon gamma gene MP:0003459 increased fear-related response IAGP N RGD:5509061 20141003 MGI PMID:10080860 737488 Ifng interferon gamma gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11714835 737488 Ifng interferon gamma gene MP:0003579 increased ovarian carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12732663 737488 Ifng interferon gamma gene MP:0003643 spleen atrophy IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0003644 thymus atrophy IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0003699 abnormal female reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:10639149 737488 Ifng interferon gamma gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:12097414 737488 Ifng interferon gamma gene MP:0003726 decreased autoantibody level IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0003957 abnormal nitric oxide homeostasis IAGP N RGD:5509061 20141003 MGI PMID:17475277 737488 Ifng interferon gamma gene MP:0004007 abnormal lung vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:10490099 737488 Ifng interferon gamma gene MP:0004256 abnormal maternal decidual layer morphology IAGP N RGD:5509061 20141003 MGI PMID:10411532 737488 Ifng interferon gamma gene MP:0004733 abnormal thoracic cavity morphology IAGP N RGD:5509061 20200611 MGI PMID:9765476 737488 Ifng interferon gamma gene MP:0004752 decreased length of allograft survival IAGP N RGD:5509061 20141003 MGI PMID:9366559 737488 Ifng interferon gamma gene MP:0004795 decreased anti-nuclear antigen antibody level IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0004798 decreased anti-double stranded DNA antibody level IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:8766573 737488 Ifng interferon gamma gene MP:0004802 decreased susceptibility to systemic lupus erythematosus IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:11714835 737488 Ifng interferon gamma gene MP:0004804 decreased susceptibility to autoimmune diabetes IAGP N RGD:5509061 20141003 MGI PMID:15613333 737488 Ifng interferon gamma gene MP:0004808 abnormal hematopoietic stem cell morphology IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0004809 increased hematopoietic stem cell number IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0004924 abnormal behavior IAGP N RGD:5509061 20200611 MGI PMID:9765476 737488 Ifng interferon gamma gene MP:0005000 abnormal immune tolerance IAGP N RGD:5509061 20141003 MGI PMID:9469425 737488 Ifng interferon gamma gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:12732663 737488 Ifng interferon gamma gene MP:0005011 increased eosinophil cell number IAGP N RGD:5509061 20141003 MGI PMID:9647244 737488 Ifng interferon gamma gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:9647244 737488 Ifng interferon gamma gene MP:0005015 increased T cell number IAGP N RGD:5509061 20141003 MGI PMID:12615659 737488 Ifng interferon gamma gene MP:0005015 increased T cell number IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:7561104 737488 Ifng interferon gamma gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:7908325 737488 Ifng interferon gamma gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:8228818 737488 Ifng interferon gamma gene MP:0005025 abnormal response to infection IAGP N RGD:5509061 20141003 MGI PMID:8892638 737488 Ifng interferon gamma gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:22723523 737488 Ifng interferon gamma gene MP:0005026 decreased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9794653 737488 Ifng interferon gamma gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:7908325 737488 Ifng interferon gamma gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:8892638 737488 Ifng interferon gamma gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:9794653 737488 Ifng interferon gamma gene MP:0005040 abnormal MHC II cell surface expression on macrophages IAGP N RGD:5509061 20141003 MGI PMID:8456300 737488 Ifng interferon gamma gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20141003 MGI PMID:11801676 737488 Ifng interferon gamma gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11714835 737488 Ifng interferon gamma gene MP:0005078 abnormal cytotoxic T cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9653090 737488 Ifng interferon gamma gene MP:0005089 decreased double-negative T cell number IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0005150 cachexia IAGP N RGD:5509061 20141003 MGI PMID:11342667 737488 Ifng interferon gamma gene MP:0005151 diffuse hepatic necrosis IAGP N RGD:5509061 20200611 MGI PMID:11864749 737488 Ifng interferon gamma gene MP:0005152 pancytopenia IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0005164 abnormal response to injury IAGP N RGD:5509061 20141003 MGI PMID:18353892 737488 Ifng interferon gamma gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20141003 MGI PMID:15257986 737488 Ifng interferon gamma gene MP:0005324 ascites IAGP N RGD:5509061 20200611 MGI PMID:9765476 737488 Ifng interferon gamma gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12097414 737488 Ifng interferon gamma gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:12615659 737488 Ifng interferon gamma gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0005351 decreased susceptibility to autoimmune disorder IAGP N RGD:5509061 20141003 MGI PMID:9647229 737488 Ifng interferon gamma gene MP:0005362 abnormal Langerhans cell physiology IAGP N RGD:5509061 20141003 MGI PMID:16818748 737488 Ifng interferon gamma gene MP:0005399 increased susceptibility to fungal infection IAGP N RGD:5509061 20141003 MGI PMID:9647244 737488 Ifng interferon gamma gene MP:0005501 abnormal skin physiology IAGP N RGD:5509061 20141003 MGI PMID:10383743 737488 Ifng interferon gamma gene MP:0005542 cornea vascularization IAGP N RGD:5509061 20141003 MGI PMID:17051153 737488 Ifng interferon gamma gene MP:0005554 decreased circulating creatinine level IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:12097414 737488 Ifng interferon gamma gene MP:0005616 decreased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:7561104 737488 Ifng interferon gamma gene MP:0005617 increased susceptibility to type IV hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:10438967 737488 Ifng interferon gamma gene MP:0005671 abnormal response to transplant IAGP N RGD:5509061 20141003 MGI PMID:9239401 737488 Ifng interferon gamma gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:9233639 737488 Ifng interferon gamma gene MP:0006269 abnormal mammary gland growth during pregnancy IAGP N RGD:5509061 20141003 MGI PMID:11445538 737488 Ifng interferon gamma gene MP:0008039 increased NK T cell number IAGP N RGD:5509061 20141003 MGI PMID:17475277 737488 Ifng interferon gamma gene MP:0008040 decreased NK T cell number IAGP N RGD:5509061 20200910 MGI PMID:30111894 737488 Ifng interferon gamma gene MP:0008054 abnormal uterine NK cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10411532 737488 Ifng interferon gamma gene MP:0008074 increased CD4-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23135404 737488 Ifng interferon gamma gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:23135404 737488 Ifng interferon gamma gene MP:0008078 increased CD8-positive, alpha-beta T cell number IAGP N RGD:5509061 20141003 MGI PMID:9973424 737488 Ifng interferon gamma gene MP:0008135 small Peyer's patches IAGP N RGD:5509061 20141003 MGI PMID:9647244 737488 Ifng interferon gamma gene MP:0008209 decreased pre-B cell number IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0008211 decreased mature B cell number IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0008255 decreased megakaryocyte cell number IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20141003 MGI PMID:9794653 737488 Ifng interferon gamma gene MP:0008474 absent spleen germinal center IAGP N RGD:5509061 20141003 MGI PMID:9647244 737488 Ifng interferon gamma gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:7908325 737488 Ifng interferon gamma gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0008496 decreased IgG2a level IAGP N RGD:5509061 20141003 MGI PMID:9647229 737488 Ifng interferon gamma gene MP:0008497 decreased IgG2b level IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:7908325 737488 Ifng interferon gamma gene MP:0008498 decreased IgG3 level IAGP N RGD:5509061 20141003 MGI PMID:9109438 737488 Ifng interferon gamma gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:12732663 737488 Ifng interferon gamma gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:7908325 737488 Ifng interferon gamma gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:8228818 737488 Ifng interferon gamma gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9647229 737488 Ifng interferon gamma gene MP:0008499 increased IgG1 level IAGP N RGD:5509061 20141003 MGI PMID:9973424 737488 Ifng interferon gamma gene MP:0008523 absent lymph node germinal center IAGP N RGD:5509061 20141003 MGI PMID:9647244 737488 Ifng interferon gamma gene MP:0008548 abnormal circulating interferon level IAGP N RGD:5509061 20200611 MGI PMID:11864749 737488 Ifng interferon gamma gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:10878379 737488 Ifng interferon gamma gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:9531602 737488 Ifng interferon gamma gene MP:0008660 increased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:9973424 737488 Ifng interferon gamma gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:10878379 737488 Ifng interferon gamma gene MP:0008661 decreased interleukin-10 secretion IAGP N RGD:5509061 20141003 MGI PMID:16818748 737488 Ifng interferon gamma gene MP:0008663 increased interleukin-12 secretion IAGP N RGD:5509061 20141003 MGI PMID:16818748 737488 Ifng interferon gamma gene MP:0008681 increased interleukin-17 secretion IAGP N RGD:5509061 20141003 MGI PMID:18322180 737488 Ifng interferon gamma gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:9973424 737488 Ifng interferon gamma gene MP:0008699 increased interleukin-4 secretion IAGP N RGD:5509061 20141003 MGI PMID:10878379 737488 Ifng interferon gamma gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:8892638 737488 Ifng interferon gamma gene MP:0008702 increased interleukin-5 secretion IAGP N RGD:5509061 20141003 MGI PMID:9973424 737488 Ifng interferon gamma gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20141003 MGI PMID:16200068 737488 Ifng interferon gamma gene MP:0008713 abnormal cytokine level IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:10490099 737488 Ifng interferon gamma gene MP:0008813 decreased common myeloid progenitor cell number IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0008828 abnormal lymph node cell ratio IAGP N RGD:5509061 20141003 MGI PMID:11067886 737488 Ifng interferon gamma gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:9647229 737488 Ifng interferon gamma gene MP:0008973 decreased erythroid progenitor cell number IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0009099 abnormal uterine NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:10411532 737488 Ifng interferon gamma gene MP:0009142 decreased prepulse inhibition IEA N RGD:5509061 20211021 MGI 737488 Ifng interferon gamma gene MP:0009246 pale spleen IAGP N RGD:5509061 20141003 MGI PMID:9531602 737488 Ifng interferon gamma gene MP:0009336 increased splenocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:8456300 737488 Ifng interferon gamma gene MP:0009394 increased uterine NK cell number IAGP N RGD:5509061 20141003 MGI PMID:10411532 737488 Ifng interferon gamma gene MP:0009395 increased nucleated erythrocyte cell number IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0009419 skeletal muscle fibrosis IAGP N RGD:5509061 20141003 MGI PMID:18353892 737488 Ifng interferon gamma gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10438967 737488 Ifng interferon gamma gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:19139386 737488 Ifng interferon gamma gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20200910 MGI PMID:30111894 737488 Ifng interferon gamma gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:15240709 737488 Ifng interferon gamma gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:7504064 737488 Ifng interferon gamma gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:7621071 737488 Ifng interferon gamma gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:8245795 737488 Ifng interferon gamma gene MP:0009788 increased susceptibility to bacterial infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9531602 737488 Ifng interferon gamma gene MP:0009828 increased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:12093877 737488 Ifng interferon gamma gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20141003 MGI PMID:9531602 737488 Ifng interferon gamma gene MP:0010210 abnormal circulating cytokine level IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:12093877 737488 Ifng interferon gamma gene MP:0010308 decreased tumor latency IAGP N RGD:5509061 20141003 MGI PMID:9653090 737488 Ifng interferon gamma gene MP:0010574 dilated aorta IAGP N RGD:5509061 20141003 MGI PMID:19139386 737488 Ifng interferon gamma gene MP:0010639 abnormal tumor pathology IAGP N RGD:5509061 20141003 MGI PMID:9653090 737488 Ifng interferon gamma gene MP:0010740 abnormal dendritic cell chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:16818748 737488 Ifng interferon gamma gene MP:0010750 increased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:7908325 737488 Ifng interferon gamma gene MP:0010750 increased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:8892638 737488 Ifng interferon gamma gene MP:0010750 increased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:9794653 737488 Ifng interferon gamma gene MP:0010751 decreased susceptibility to parasitic infection induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:22723523 737488 Ifng interferon gamma gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:12097414 737488 Ifng interferon gamma gene MP:0010760 abnormal macrophage chemotaxis IAGP N RGD:5509061 20141003 MGI PMID:18353892 737488 Ifng interferon gamma gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:8456300 737488 Ifng interferon gamma gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9653090 737488 Ifng interferon gamma gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9834083 737488 Ifng interferon gamma gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12732663 737488 Ifng interferon gamma gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737488 Ifng interferon gamma gene MP:0011178 increased erythroblast number IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0011320 abnormal glomerular capillary morphology IAGP N RGD:5509061 20141003 MGI PMID:12097414 737488 Ifng interferon gamma gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:12097414 737488 Ifng interferon gamma gene MP:0012431 increased lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:12093877 737488 Ifng interferon gamma gene MP:0013239 impaired skeletal muscle regeneration IAGP N RGD:5509061 20141003 MGI PMID:18353892 737488 Ifng interferon gamma gene MP:0013292 embryonic lethality prior to organogenesis IEA N RGD:5509061 20201231 MGI 737488 Ifng interferon gamma gene MP:0013293 embryonic lethality prior to tooth bud stage IEA N RGD:5509061 20201231 MGI 737488 Ifng interferon gamma gene MP:0013414 decreased myeloid cell number in bone marrow IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0013590 enlarged thymus medulla IAGP N RGD:5509061 20150319 MGI PMID:10490099 737488 Ifng interferon gamma gene MP:0013697 decreased granulocyte monocyte progenitor cell number IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0013705 decreased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20160929 MGI PMID:25342713 737488 Ifng interferon gamma gene MP:0020916 increased susceptibility to Herpesvirales infection IAGP N RGD:5509061 20200430 MGI PMID:7561104 737488 Ifng interferon gamma gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200430 MGI PMID:9973424 737488 Ifng interferon gamma gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200611 MGI PMID:11864749 737488 Ifng interferon gamma gene MP:0020949 increased susceptibility to Coronaviridae infection IAGP N RGD:5509061 20200611 MGI PMID:9765476 737488 Ifng interferon gamma gene MP:0030466 alveolar process atrophy IAGP N RGD:5509061 20171221 MGI PMID:17305866 737488 Ifng interferon gamma gene MP:0030960 abnormal diapedesis IAGP N RGD:5509061 20190725 MGI PMID:11714835 737488 Ifng interferon gamma gene MP:0031026 increased susceptibility to Herpesvirales infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:7561104 737488 Ifng interferon gamma gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200514 MGI PMID:9973424 737488 Ifng interferon gamma gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200611 MGI PMID:11864749 737488 Ifng interferon gamma gene MP:0031048 increased susceptibility to Coronaviridae infection induced morbidity/mortality IAGP N RGD:5509061 20200611 MGI PMID:9765476 737488 Ifng interferon gamma gene MP:0031274 increased susceptibility to induced aneurysm formation IAGP N RGD:5509061 20210617 MGI PMID:19139386 737490 Csrp1 cysteine and glycine-rich protein 1 gene MP:0004883 abnormal vascular wound healing IAGP N RGD:5509061 20141003 MGI PMID:20056913 737493 Itih4 inter alpha-trypsin inhibitor, heavy chain 4 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:18263735 737493 Itih4 inter alpha-trypsin inhibitor, heavy chain 4 gene MP:0004001 decreased hepatocyte proliferation IAGP N RGD:5509061 20141003 MGI PMID:18263735 737493 Itih4 inter alpha-trypsin inhibitor, heavy chain 4 gene MP:0008891 decreased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18263735 737493 Itih4 inter alpha-trypsin inhibitor, heavy chain 4 gene MP:0010266 decreased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:18263735 737493 Itih4 inter alpha-trypsin inhibitor, heavy chain 4 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 737495 Fxyd7 FXYD domain-containing ion transport regulator 7 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20231207 MGI 737500 Homer1 homer scaffolding protein 1 gene MP:0001968 abnormal touch/ nociception IAGP N RGD:5509061 20141003 MGI PMID:19265511 737500 Homer1 homer scaffolding protein 1 gene MP:0002693 abnormal pancreas physiology IAGP N RGD:5509061 20141003 MGI PMID:14505576 737500 Homer1 homer scaffolding protein 1 gene MP:0002736 abnormal nociception after inflammation IAGP N RGD:5509061 20141003 MGI PMID:22561452 737500 Homer1 homer scaffolding protein 1 gene MP:0003633 abnormal nervous system physiology IAGP N RGD:5509061 20141003 MGI PMID:15294147 737500 Homer1 homer scaffolding protein 1 gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:21172614 737500 Homer1 homer scaffolding protein 1 gene MP:0008143 abnormal dendrite morphology IAGP N RGD:5509061 20141003 MGI PMID:19265511 737500 Homer1 homer scaffolding protein 1 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:19265511 737500 Homer1 homer scaffolding protein 1 gene MP:0008874 decreased physiological sensitivity to xenobiotic IAGP N RGD:5509061 20141003 MGI PMID:21172614 737500 Homer1 homer scaffolding protein 1 gene MP:0009454 impaired contextual conditioning behavior IAGP N RGD:5509061 20141003 MGI PMID:19265511 737500 Homer1 homer scaffolding protein 1 gene MP:0009713 enhanced conditioned place preference behavior IAGP N RGD:5509061 20141003 MGI PMID:15294147 737500 Homer1 homer scaffolding protein 1 gene MP:0009754 enhanced behavioral response to cocaine IAGP N RGD:5509061 20141003 MGI PMID:15294147 737502 Pkm pyruvate kinase, muscle gene MP:0001272 increased metastatic potential IAGP N RGD:5509061 20141003 MGI PMID:24120138 737502 Pkm pyruvate kinase, muscle gene MP:0001693 failure of primitive streak formation IEA N RGD:5509061 20241010 MGI 737502 Pkm pyruvate kinase, muscle gene MP:0001694 absent egg cylinders IEA N RGD:5509061 20241010 MGI 737502 Pkm pyruvate kinase, muscle gene MP:0001696 failure to gastrulate IEA N RGD:5509061 20241010 MGI 737502 Pkm pyruvate kinase, muscle gene MP:0001697 abnormal embryo size IEA N RGD:5509061 20230601 MGI 737502 Pkm pyruvate kinase, muscle gene MP:0001698 decreased embryo size IEA N RGD:5509061 20241010 MGI 737502 Pkm pyruvate kinase, muscle gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24120138 737502 Pkm pyruvate kinase, muscle gene MP:0003984 embryonic growth retardation IEA N RGD:5509061 20230601 MGI 737502 Pkm pyruvate kinase, muscle gene MP:0008019 increased liver tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24120138 737502 Pkm pyruvate kinase, muscle gene MP:0009331 absent primitive node IEA N RGD:5509061 20241010 MGI 737502 Pkm pyruvate kinase, muscle gene MP:0010299 increased mammary gland tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:24120138 737502 Pkm pyruvate kinase, muscle gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:7262549 737502 Pkm pyruvate kinase, muscle gene MP:0011093 embryonic lethality at implantation, complete penetrance IEA N RGD:5509061 20111116 MGI 737502 Pkm pyruvate kinase, muscle gene MP:0011095 embryonic lethality between implantation and placentation, complete penetrance IEA N RGD:5509061 20241017 MGI 737502 Pkm pyruvate kinase, muscle gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20220811 MGI 737502 Pkm pyruvate kinase, muscle gene MP:0012724 absent head fold IEA N RGD:5509061 20241010 MGI 737502 Pkm pyruvate kinase, muscle gene MP:0014237 decreased tumor-free survival time IAGP N RGD:5509061 20230608 MGI PMID:24120138 737504 Srd5a2 steroid 5 alpha-reductase 2 gene MP:0000664 small prostate gland anterior lobe IAGP N RGD:5509061 20141003 MGI PMID:11606430 737504 Srd5a2 steroid 5 alpha-reductase 2 gene MP:0000689 abnormal spleen morphology IEA N RGD:5509061 20201022 MGI 737504 Srd5a2 steroid 5 alpha-reductase 2 gene MP:0000691 enlarged spleen IEA N RGD:5509061 20201022 MGI 737504 Srd5a2 steroid 5 alpha-reductase 2 gene MP:0000692 small spleen IEA N RGD:5509061 20210520 MGI 737504 Srd5a2 steroid 5 alpha-reductase 2 gene MP:0001157 small seminal vesicle IAGP N RGD:5509061 20141003 MGI PMID:11606430 737504 Srd5a2 steroid 5 alpha-reductase 2 gene MP:0001325 abnormal retina morphology IEA N RGD:5509061 20240523 MGI 737504 Srd5a2 steroid 5 alpha-reductase 2 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:11606430 737504 Srd5a2 steroid 5 alpha-reductase 2 gene MP:0002060 abnormal skin morphology IEA N RGD:5509061 20201022 MGI 737504 Srd5a2 steroid 5 alpha-reductase 2 gene MP:0002774 small prostate gland IAGP N RGD:5509061 20141003 MGI PMID:11606430 737504 Srd5a2 steroid 5 alpha-reductase 2 gene MP:0002907 abnormal parturition IAGP N RGD:5509061 20141003 MGI PMID:11606430 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0000157 abnormal sternum morphology IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:16096649 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210128 MGI 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0002024 increased T cell derived lymphoma incidence IAGP N RGD:5509061 20141003 MGI PMID:16096649 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0002026 increased leukemia incidence IAGP N RGD:5509061 20141003 MGI PMID:16096649 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0002084 abnormal developmental patterning IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0002356 abnormal spleen red pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:16096649 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0002357 abnormal spleen white pulp morphology IAGP N RGD:5509061 20141003 MGI PMID:16096649 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0003036 vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0003047 abnormal thoracic vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0003048 abnormal cervical vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0003179 thrombocytopenia IEA N RGD:5509061 20170105 MGI 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0003345 decreased rib number IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0003918 decreased kidney weight IEA N RGD:5509061 20201022 MGI 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0004607 abnormal cervical atlas morphology IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0004608 abnormal cervical axis morphology IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0004615 cervical vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0004618 thoracic vertebral transformation IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0004620 cervical vertebral fusion IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0004648 decreased thoracic vertebrae number IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0004703 abnormal vertebral column morphology IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0005298 abnormal clavicle morphology IEA N RGD:5509061 20201231 MGI 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0008277 abnormal sternum ossification IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0008806 increased circulating amylase level IEA N RGD:5509061 20211021 MGI 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0008922 abnormal cervical rib IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0010296 increased hemolymphoid system tumor incidence IAGP N RGD:5509061 20141003 MGI PMID:16096649 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12242306 737508 Mllt3 myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737509 Glg1 golgi apparatus protein 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0000150 abnormal rib morphology IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:20530870 737509 Glg1 golgi apparatus protein 1 gene MP:0001533 abnormal skeleton physiology IAGP N RGD:5509061 20141003 MGI PMID:20530870 737509 Glg1 golgi apparatus protein 1 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20211021 MGI 737509 Glg1 golgi apparatus protein 1 gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0002759 abnormal caudal vertebrae morphology IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0003443 increased circulating glycerol level IEA N RGD:5509061 20210128 MGI 737509 Glg1 golgi apparatus protein 1 gene MP:0003628 abnormal leukocyte adhesion IAGP N RGD:5509061 20151231 MGI PMID:22939356 737509 Glg1 golgi apparatus protein 1 gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:20530870 737509 Glg1 golgi apparatus protein 1 gene MP:0003799 impaired macrophage chemotaxis IAGP N RGD:5509061 20151231 MGI PMID:22939356 737509 Glg1 golgi apparatus protein 1 gene MP:0003884 decreased macrophage cell number IAGP N RGD:5509061 20151231 MGI PMID:22939356 737509 Glg1 golgi apparatus protein 1 gene MP:0004173 abnormal intervertebral disk morphology IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0004174 abnormal spine curvature IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20141003 MGI PMID:20530870 737509 Glg1 golgi apparatus protein 1 gene MP:0004538 abnormal maxillary shelf morphology IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0004599 abnormal vertebral arch morphology IEA N RGD:5509061 20201231 MGI 737509 Glg1 golgi apparatus protein 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20151231 MGI PMID:22939356 737509 Glg1 golgi apparatus protein 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:20530870 737509 Glg1 golgi apparatus protein 1 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0009247 meteorism IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0009431 decreased fetal weight IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20141003 MGI PMID:20530870 737509 Glg1 golgi apparatus protein 1 gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:20530870 737509 Glg1 golgi apparatus protein 1 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20151231 MGI PMID:22939356 737509 Glg1 golgi apparatus protein 1 gene MP:0010103 small thoracic cage IAGP N RGD:5509061 20141003 MGI PMID:20530870 737509 Glg1 golgi apparatus protein 1 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20023171 737509 Glg1 golgi apparatus protein 1 gene MP:0011092 embryonic lethality, complete penetrance IAGP N RGD:5509061 20151231 MGI PMID:22939356 737509 Glg1 golgi apparatus protein 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 737509 Glg1 golgi apparatus protein 1 gene MP:0020253 increased collagen level IAGP N RGD:5509061 20151231 MGI PMID:22939356 737509 Glg1 golgi apparatus protein 1 gene MP:0020333 enhanced leukocyte tethering or rolling IAGP N RGD:5509061 20160915 MGI PMID:22939356 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20186915 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0000774 decreased brain size IAGP N RGD:5509061 20141003 MGI PMID:20186915 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:20186915 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20240502 MGI PMID:37275776 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0001265 decreased body size IAGP N RGD:5509061 20240502 MGI PMID:37275776 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0001364 decreased anxiety-related response IEA N RGD:5509061 20210520 MGI 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0001392 abnormal locomotor behavior IAGP N RGD:5509061 20240502 MGI PMID:37275776 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210520 MGI 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20240502 MGI PMID:37275776 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0001436 abnormal suckling behavior IAGP N RGD:5509061 20141003 MGI PMID:20186915 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0001523 impaired righting response IAGP N RGD:5509061 20240502 MGI PMID:37275776 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:20186915 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0002152 abnormal brain morphology IAGP N RGD:5509061 20141003 MGI PMID:20186915 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0002193 minimal clonic seizures IAGP N RGD:5509061 20240502 MGI PMID:37275776 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210520 MGI 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0003731 abnormal retina outer nuclear layer morphology IEA N RGD:5509061 20210520 MGI 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0004261 abnormal embryonic neuroepithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:20186915 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0004948 abnormal neuronal precursor proliferation IAGP N RGD:5509061 20141003 MGI PMID:20186915 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0005657 abnormal neural plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20186915 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0006254 thin cerebral cortex IAGP N RGD:5509061 20141003 MGI PMID:20186915 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0008432 abnormal long-term spatial reference memory IAGP N RGD:5509061 20240502 MGI PMID:37275776 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0008458 abnormal cortical ventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:20186915 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0008779 abnormal maternal behavior IAGP N RGD:5509061 20240502 MGI PMID:37275776 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0008797 facial cleft IEA N RGD:5509061 20210520 MGI 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20240502 MGI PMID:37275776 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0009937 abnormal neuron differentiation IAGP N RGD:5509061 20141003 MGI PMID:20186915 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0010123 increased bone mineral content IEA N RGD:5509061 20210128 MGI 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20186915 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20240502 MGI PMID:37275776 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20186915 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0011965 decreased total retina thickness IEA N RGD:5509061 20210128 MGI 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20240502 MGI PMID:37275776 737510 Gnb1 guanine nucleotide binding protein (G protein), beta 1 gene MP:0020351 decreased vocalization IAGP N RGD:5509061 20240502 MGI PMID:37275776 737511 Nphs1 nephrosis 1, nephrin gene MP:0000522 kidney cortex cyst IAGP N RGD:5509061 20141003 MGI PMID:11136707 737511 Nphs1 nephrosis 1, nephrin gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:11136707 737511 Nphs1 nephrosis 1, nephrin gene MP:0002135 abnormal kidney morphology IAGP N RGD:5509061 20141003 MGI PMID:12904583 737511 Nphs1 nephrosis 1, nephrin gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20151112 MGI 737511 Nphs1 nephrosis 1, nephrin gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:12039968 737511 Nphs1 nephrosis 1, nephrin gene MP:0002705 dilated renal tubule IAGP N RGD:5509061 20141003 MGI PMID:12039988 737511 Nphs1 nephrosis 1, nephrin gene MP:0002871 albuminuria IAGP N RGD:5509061 20141003 MGI PMID:11136707 737511 Nphs1 nephrosis 1, nephrin gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:11136707 737511 Nphs1 nephrosis 1, nephrin gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:12039968 737511 Nphs1 nephrosis 1, nephrin gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20141003 MGI PMID:12039988 737511 Nphs1 nephrosis 1, nephrin gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20191219 MGI PMID:27707879 737511 Nphs1 nephrosis 1, nephrin gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20201022 MGI PMID:27430022 737511 Nphs1 nephrosis 1, nephrin gene MP:0003068 enlarged kidney IAGP N RGD:5509061 20141003 MGI PMID:11136707 737511 Nphs1 nephrosis 1, nephrin gene MP:0003670 dilated renal glomerular capsule IAGP N RGD:5509061 20141003 MGI PMID:12039988 737511 Nphs1 nephrosis 1, nephrin gene MP:0003917 increased kidney weight IAGP N RGD:5509061 20141003 MGI PMID:11136707 737511 Nphs1 nephrosis 1, nephrin gene MP:0005264 glomerulosclerosis IAGP N RGD:5509061 20191219 MGI PMID:27707879 737511 Nphs1 nephrosis 1, nephrin gene MP:0005325 abnormal renal glomerulus morphology IAGP N RGD:5509061 20141003 MGI PMID:12039988 737511 Nphs1 nephrosis 1, nephrin gene MP:0005326 abnormal podocyte morphology IAGP N RGD:5509061 20191219 MGI PMID:27707879 737511 Nphs1 nephrosis 1, nephrin gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:11136707 737511 Nphs1 nephrosis 1, nephrin gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20141003 MGI PMID:12039988 737511 Nphs1 nephrosis 1, nephrin gene MP:0008059 abnormal podocyte foot process morphology IAGP N RGD:5509061 20201022 MGI PMID:27430022 737511 Nphs1 nephrosis 1, nephrin gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20191219 MGI PMID:27707879 737511 Nphs1 nephrosis 1, nephrin gene MP:0008060 abnormal podocyte slit diaphragm morphology IAGP N RGD:5509061 20201022 MGI PMID:27430022 737511 Nphs1 nephrosis 1, nephrin gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20141003 MGI PMID:11136707 737511 Nphs1 nephrosis 1, nephrin gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20141003 MGI PMID:12039968 737511 Nphs1 nephrosis 1, nephrin gene MP:0008061 absent podocyte slit diaphragm IAGP N RGD:5509061 20141003 MGI PMID:12039988 737511 Nphs1 nephrosis 1, nephrin gene MP:0008062 abnormal podocyte slit junction morphology IAGP N RGD:5509061 20141003 MGI PMID:12039988 737511 Nphs1 nephrosis 1, nephrin gene MP:0008139 fused podocyte foot processes IAGP N RGD:5509061 20141003 MGI PMID:12039988 737511 Nphs1 nephrosis 1, nephrin gene MP:0008140 podocyte foot process effacement IAGP N RGD:5509061 20141003 MGI PMID:11136707 737511 Nphs1 nephrosis 1, nephrin gene MP:0009050 dilated proximal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:11136707 737511 Nphs1 nephrosis 1, nephrin gene MP:0009051 dilated distal convoluted tubule IAGP N RGD:5509061 20141003 MGI PMID:11136707 737511 Nphs1 nephrosis 1, nephrin gene MP:0010107 abnormal renal reabsorption IAGP N RGD:5509061 20201022 MGI PMID:27430022 737511 Nphs1 nephrosis 1, nephrin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12039968 737511 Nphs1 nephrosis 1, nephrin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12039988 737511 Nphs1 nephrosis 1, nephrin gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20201022 MGI PMID:27430022 737511 Nphs1 nephrosis 1, nephrin gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11136707 737511 Nphs1 nephrosis 1, nephrin gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12039988 737511 Nphs1 nephrosis 1, nephrin gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20201022 MGI PMID:27430022 737511 Nphs1 nephrosis 1, nephrin gene MP:0011307 kidney medulla cyst IAGP N RGD:5509061 20141003 MGI PMID:11136707 737511 Nphs1 nephrosis 1, nephrin gene MP:0011353 expanded mesangial matrix IAGP N RGD:5509061 20141003 MGI PMID:12039988 737511 Nphs1 nephrosis 1, nephrin gene MP:0011377 renal glomerulus fibrosis IAGP N RGD:5509061 20141003 MGI PMID:12039988 737511 Nphs1 nephrosis 1, nephrin gene MP:0011427 increased mesangial cell number IAGP N RGD:5509061 20141003 MGI PMID:11136707 737511 Nphs1 nephrosis 1, nephrin gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:11136707 737511 Nphs1 nephrosis 1, nephrin gene MP:0011501 increased glomerular capsule space IAGP N RGD:5509061 20141003 MGI PMID:12039968 737511 Nphs1 nephrosis 1, nephrin gene MP:0011753 decreased podocyte number IAGP N RGD:5509061 20191219 MGI PMID:27707879 737512 Gstt2 glutathione S-transferase, theta 2 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0001263 weight loss IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0002080 prenatal lethality IEA N RGD:5509061 20230119 MGI 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0003141 cardiac fibrosis IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0003819 increased left ventricle diastolic pressure IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0003822 decreased left ventricle systolic pressure IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0003913 increased heart right ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0003915 increased heart left ventricle weight IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0004084 abnormal cardiac muscle relaxation IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0006035 abnormal mitochondrial morphology IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0008772 increased heart ventricle size IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0010563 increased heart right ventricle size IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0010579 increased heart left ventricle size IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0010955 abnormal respiratory electron transport chain IAGP N RGD:5509061 20141003 MGI PMID:22474353 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20230119 MGI 737515 Ndufs6 NADH:ubiquinone oxidoreductase core subunit S6 gene MP:0011631 decreased mitochondrial size IAGP N RGD:5509061 20141003 MGI PMID:22474353 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11162635 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000182 increased circulating LDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000186 decreased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000218 increased leukocyte cell number IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000221 decreased leukocyte cell number IEA N RGD:5509061 20210128 MGI 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000230 abnormal systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15178650 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000231 hypertension IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000321 increased bone marrow cell number IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000322 increased granulocyte number IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000599 enlarged liver IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000603 pale liver IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000609 abnormal liver physiology IAGP N RGD:5509061 20141003 MGI PMID:10862797 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000613 abnormal salivary gland morphology IAGP N RGD:5509061 20150618 MGI PMID:25447050 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000659 prostate gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11356695 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000693 spleen hyperplasia IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0000745 tremors IEA N RGD:5509061 20210826 MGI 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001121 uterus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:10875266 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:12205030 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001126 abnormal ovary morphology IAGP N RGD:5509061 20141003 MGI PMID:9826549 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:10875266 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:12205030 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001129 impaired ovarian folliculogenesis IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:10875266 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:12205030 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20141003 MGI PMID:9826549 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001145 abnormal male reproductive system morphology IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001152 increased Leydig cell number IAGP N RGD:5509061 20141003 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:11545296 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:12553872 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001260 increased body weight IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001261 obese IAGP N RGD:5509061 20141003 MGI PMID:12553872 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001261 obese IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001363 increased anxiety-related response IEA N RGD:5509061 20220519 MGI 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001377 abnormal mating frequency IAGP N RGD:5509061 20141003 MGI PMID:11545296 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001380 reduced male mating frequency IAGP N RGD:5509061 20141003 MGI PMID:11545296 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001402 decreased locomotor activity IEA N RGD:5509061 20210128 MGI 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20210826 MGI 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001417 decreased exploration in new environment IEA N RGD:5509061 20220519 MGI 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001441 increased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:16566897 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12553872 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10875266 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001750 increased circulating follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:10875266 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001751 increased circulating luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001859 kidney inflammation IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001870 salivary gland inflammation IAGP N RGD:5509061 20150618 MGI PMID:25447050 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001919 abnormal reproductive system physiology IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11241177 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:11545296 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12845227 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:9826549 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:12845227 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:10875266 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11241177 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:9826549 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0001932 abnormal spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002016 ovary cyst IAGP N RGD:5509061 20141003 MGI PMID:12205030 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002075 abnormal coat/hair pigmentation IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:10862797 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:19804754 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002211 abnormal primary sex determination IAGP N RGD:5509061 20141003 MGI PMID:12205030 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002359 abnormal spleen germinal center morphology IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002493 increased IgG level IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002566 abnormal sexual interaction IAGP N RGD:5509061 20141003 MGI PMID:12845227 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002572 abnormal emotion/affect behavior IAGP N RGD:5509061 20141003 MGI PMID:16566897 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:15178650 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:10862797 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002628 hepatic steatosis IAGP N RGD:5509061 20141003 MGI PMID:12553872 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002631 abnormal epididymis morphology IAGP N RGD:5509061 20141003 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002637 small uterus IAGP N RGD:5509061 20141003 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002675 asthenozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11545296 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:11545296 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002777 absent ovarian follicles IAGP N RGD:5509061 20141003 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:11162635 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:11241177 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:11356695 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:12553872 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002781 increased circulating testosterone level IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002808 abnormal barbering behavior IAGP N RGD:5509061 20141003 MGI PMID:16566897 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002842 increased systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002962 increased urine protein level IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002965 increased circulating serum albumin level IEA N RGD:5509061 20211021 MGI 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002966 decreased circulating alkaline phosphatase level IEA N RGD:5509061 20210128 MGI 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002970 abnormal white adipose tissue morphology IAGP N RGD:5509061 20150618 MGI PMID:25447050 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0002981 increased liver weight IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:16566897 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0003356 impaired luteinization IAGP N RGD:5509061 20141003 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0003509 increased circulating dihydrotestosterone level IAGP N RGD:5509061 20141003 MGI PMID:11356695 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0003511 abnormal labium morphology IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0003529 enlarged clitoris IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0003572 abnormal uterus development IAGP N RGD:5509061 20141003 MGI PMID:10875266 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0003572 abnormal uterus development IAGP N RGD:5509061 20141003 MGI PMID:9826549 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0003607 abnormal prostate gland physiology IAGP N RGD:5509061 20141003 MGI PMID:11356695 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0003725 increased autoantibody level IAGP N RGD:5509061 20150618 MGI PMID:25447050 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:11162635 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0003862 decreased aggression towards male mice IAGP N RGD:5509061 20141003 MGI PMID:12845227 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0003929 decreased heart rate variability IAGP N RGD:5509061 20141003 MGI PMID:15178650 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20141003 MGI PMID:11162635 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004184 abnormal baroreceptor physiology IAGP N RGD:5509061 20141003 MGI PMID:15178650 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:18317592 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004771 increased anti-single stranded DNA antibody level IAGP N RGD:5509061 20150618 MGI PMID:25447050 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:10875266 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004834 ovary hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:12205030 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004876 decreased mean systemic arterial blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15178650 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004901 decreased male germ cell number IAGP N RGD:5509061 20141003 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:10875266 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:11162635 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004905 decreased uterus weight IAGP N RGD:5509061 20141003 MGI PMID:9826549 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004909 increased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:11162635 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004909 increased seminal vesicle weight IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004958 enlarged prostate gland IAGP N RGD:5509061 20141003 MGI PMID:11356695 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004961 increased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:11356695 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004961 increased prostate gland weight IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:11162635 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0004992 increased bone resorption IAGP N RGD:5509061 20141003 MGI PMID:11162635 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005013 increased lymphocyte cell number IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005014 increased B cell number IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20210128 MGI 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005124 increased circulating prolactin level IAGP N RGD:5509061 20141003 MGI PMID:11356695 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005145 increased circulating VLDL cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005156 bradykinesia IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12553872 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:11162635 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005181 decreased circulating estradiol level IAGP N RGD:5509061 20141003 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12553872 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005305 prostate gland anterior lobe hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:11356695 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:10862797 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005319 abnormal enzyme/coenzyme level IAGP N RGD:5509061 20141003 MGI PMID:15178650 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12553872 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005350 increased susceptibility to autoimmune disorder IAGP N RGD:5509061 20150618 MGI PMID:25447050 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005425 increased macrophage cell number IAGP N RGD:5509061 20150618 MGI PMID:25447050 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005455 increased susceptibility to weight gain IAGP N RGD:5509061 20141003 MGI PMID:12553872 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005505 thrombocytosis IEA N RGD:5509061 20210128 MGI 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:12553872 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005559 increased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005599 increased cardiac muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15178650 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IEA N RGD:5509061 20220811 MGI 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005656 decreased aggression IAGP N RGD:5509061 20141003 MGI PMID:11182758 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0005669 increased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0006094 increased fat cell size IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0006263 decreased systemic arterial diastolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15178650 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0006362 abnormal male germ cell morphology IAGP N RGD:5509061 20141003 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0006380 abnormal spermatid morphology IAGP N RGD:5509061 20141003 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0008126 increased dendritic cell number IAGP N RGD:5509061 20150618 MGI PMID:25447050 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0008210 increased mature B cell number IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0008257 thin myometrium IAGP N RGD:5509061 20141003 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0008258 thin endometrium IAGP N RGD:5509061 20141003 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0008279 arrest of spermiogenesis IAGP N RGD:5509061 20141003 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0008431 abnormal short-term spatial reference memory IAGP N RGD:5509061 20141003 MGI PMID:14561933 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0008466 enlarged mesenteric lymph nodes IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0008553 increased circulating tumor necrosis factor level IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0008596 increased circulating interleukin-6 level IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:10875266 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0008869 anovulation IAGP N RGD:5509061 20141003 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0008880 lacrimal gland inflammation IAGP N RGD:5509061 20150618 MGI PMID:25447050 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0008987 abnormal liver lobule morphology IAGP N RGD:5509061 20141003 MGI PMID:10862797 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12553872 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0009285 increased gonadal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:10862797 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0009286 increased abdominal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12553872 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0009296 increased mammary fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:9618522 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0009302 increased renal fat pad weight IAGP N RGD:5509061 20141003 MGI PMID:12553872 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0009363 abnormal tertiary ovarian follicle morphology IAGP N RGD:5509061 20220407 MGI PMID:12205030 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0009364 abnormal mature ovarian follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12205030 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0009444 ovarian follicular cyst IAGP N RGD:5509061 20220407 MGI PMID:10875266 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0009516 enlarged salivary gland IAGP N RGD:5509061 20150618 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0009697 abnormal copulation behavior IAGP N RGD:5509061 20141003 MGI PMID:12845227 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0009856 failure of ejaculation IAGP N RGD:5509061 20141003 MGI PMID:12845227 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:11070087 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0010024 increased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:9826549 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0010867 abnormal bone trabecula morphology IAGP N RGD:5509061 20141003 MGI PMID:11162635 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0011572 abnormal aorta bulb morphology IAGP N RGD:5509061 20141003 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0011750 abnormal seminiferous tubule epithelium morphology IAGP N RGD:5509061 20141003 MGI PMID:11241177 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0013141 sexually aggressive behavior IAGP N RGD:5509061 20240718 MGI PMID:9826549 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0013141 sexually aggressive behavior IAGP N RGD:5509061 20240905 MGI PMID:12845227 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20230601 MGI 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0013507 increased ovary apoptosis IAGP N RGD:5509061 20150219 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0013508 increased granulosa cell apoptosis IAGP N RGD:5509061 20150212 MGI PMID:10875266 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20220623 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20220915 MGI PMID:11162635 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0020411 increased abdominal adipose tissue amount IAGP N RGD:5509061 20170202 MGI PMID:25447050 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0020519 renal glomerular immunoglobulin deposits IAGP N RGD:5509061 20180125 MGI PMID:15314222 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20220623 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0021118 abnormal paternal behavior IAGP N RGD:5509061 20240905 MGI PMID:12845227 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0031059 increased circulating C-reactive protein level IAGP N RGD:5509061 20201002 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0031271 increased susceptibility to age-related hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:22185842 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0031354 abnormal acrosome assembly IAGP N RGD:5509061 20220303 MGI PMID:10393934 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0031361 increased prostate gland anterior lobe weight IAGP N RGD:5509061 20220303 MGI PMID:11356695 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0031364 increased prostate gland ventral lobe weight IAGP N RGD:5509061 20220303 MGI PMID:11356695 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0031365 prostate gland ventral lobe hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:11356695 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0031368 increased prostate gland dorsolateral lobe weight IAGP N RGD:5509061 20220303 MGI PMID:11356695 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0031369 prostate gland dorsolateral lobe hyperplasia IAGP N RGD:5509061 20220303 MGI PMID:11356695 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0031422 failure of superovulation IAGP N RGD:5509061 20220804 MGI PMID:11431142 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0031628 abnormal intromission IAGP N RGD:5509061 20240704 MGI PMID:12845227 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0031650 decreased mounting behavior IAGP N RGD:5509061 20240905 MGI PMID:11241177 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0031650 decreased mounting behavior IAGP N RGD:5509061 20240905 MGI PMID:12845227 737520 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1 gene MP:0031650 decreased mounting behavior IAGP N RGD:5509061 20240905 MGI PMID:9826549 737526 Capn2 calpain 2 gene MP:0000259 abnormal vascular development IAGP N RGD:5509061 20141003 MGI PMID:21791606 737526 Capn2 calpain 2 gene MP:0000280 thin ventricular wall IAGP N RGD:5509061 20141003 MGI PMID:21791606 737526 Capn2 calpain 2 gene MP:0001716 abnormal placenta labyrinth morphology IAGP N RGD:5509061 20141003 MGI PMID:21791606 737526 Capn2 calpain 2 gene MP:0001914 hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:21791606 737526 Capn2 calpain 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:21791606 737526 Capn2 calpain 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:21791606 737526 Capn2 calpain 2 gene MP:0004179 transmission ratio distortion IAGP N RGD:5509061 20160804 MGI PMID:16433929 737526 Capn2 calpain 2 gene MP:0004266 pale placenta IAGP N RGD:5509061 20141003 MGI PMID:21791606 737526 Capn2 calpain 2 gene MP:0009781 abnormal preimplantation embryo development IAGP N RGD:5509061 20141003 MGI PMID:16433929 737526 Capn2 calpain 2 gene MP:0010769 abnormal survival IAGP N RGD:5509061 20141003 MGI PMID:21791606 737526 Capn2 calpain 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21791606 737526 Capn2 calpain 2 gene MP:0011094 embryonic lethality before implantation, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16433929 737526 Capn2 calpain 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21791606 737526 Capn2 calpain 2 gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:21791606 737529 Gpr6 G protein-coupled receptor 6 gene MP:0002062 abnormal associative learning IAGP N RGD:5509061 20141003 MGI PMID:17934457 737529 Gpr6 G protein-coupled receptor 6 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 737529 Gpr6 G protein-coupled receptor 6 gene MP:0004077 abnormal striatum morphology IAGP N RGD:5509061 20141003 MGI PMID:17934457 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0000352 decreased cell proliferation IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:16782887 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0000930 wavy neural tube IAGP N RGD:5509061 20141003 MGI PMID:16782887 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:16782887 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0001614 abnormal blood vessel morphology IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0001622 abnormal vasculogenesis IEA N RGD:5509061 20111116 MGI 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0001636 irregular heartbeat IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0001688 abnormal somite development IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0001698 decreased embryo size IAGP N RGD:5509061 20170427 MGI PMID:19808661 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0001719 absent vitelline blood vessels IAGP N RGD:5509061 20141003 MGI PMID:16782887 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0001726 abnormal allantois morphology IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:16782887 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0002128 abnormal blood circulation IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0002151 abnormal neural tube morphology IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16782887 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:19808661 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0003229 abnormal vitelline vasculature morphology IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0003232 abnormal forebrain development IAGP N RGD:5509061 20141003 MGI PMID:16782887 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:16782887 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0003400 kinked neural tube IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0003651 abnormal axon extension IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:16782887 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0003984 embryonic growth retardation IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:16782887 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0004180 failure of initiation of embryo turning IAGP N RGD:5509061 20170427 MGI PMID:19808661 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0004557 dilated allantois IAGP N RGD:5509061 20141003 MGI PMID:16782887 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0004560 abnormal chorionic plate morphology IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0005033 abnormal trophoblast giant cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0008554 decreased circulating tumor necrosis factor level IEA N RGD:5509061 20111116 MGI 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0008597 decreased circulating interleukin-6 level IEA N RGD:5509061 20111116 MGI 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0008721 abnormal chemokine level IEA N RGD:5509061 20111116 MGI 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0008734 decreased susceptibility to endotoxin shock IEA N RGD:5509061 20111116 MGI 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0008762 embryonic lethality IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:16782887 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0009657 failure of chorioallantoic fusion IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0011091 prenatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17628547 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:16782887 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:19808661 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0011098 embryonic lethality during organogenesis, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20111116 MGI 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0011186 abnormal visceral endoderm morphology IAGP N RGD:5509061 20141003 MGI PMID:19808661 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0012505 increased neural tube apoptosis IAGP N RGD:5509061 20141003 MGI PMID:20079728 737530 Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 gene MP:0020515 abnormal visceral yolk sac endoderm morphology IAGP N RGD:5509061 20180125 MGI PMID:19808661 737531 Gde1 glycerophosphodiester phosphodiesterase 1 gene MP:0001406 abnormal gait IEA N RGD:5509061 20181227 MGI 737531 Gde1 glycerophosphodiester phosphodiesterase 1 gene MP:0001489 decreased startle reflex IEA N RGD:5509061 20210128 MGI 737531 Gde1 glycerophosphodiester phosphodiesterase 1 gene MP:0002574 increased vertical activity IEA N RGD:5509061 20210128 MGI 737531 Gde1 glycerophosphodiester phosphodiesterase 1 gene MP:0002591 decreased mean corpuscular volume IEA N RGD:5509061 20210520 MGI 737531 Gde1 glycerophosphodiester phosphodiesterase 1 gene MP:0002757 decreased vertical activity IEA N RGD:5509061 20210128 MGI 737531 Gde1 glycerophosphodiester phosphodiesterase 1 gene MP:0002968 increased circulating alkaline phosphatase level IEA N RGD:5509061 20211021 MGI 737531 Gde1 glycerophosphodiester phosphodiesterase 1 gene MP:0004924 abnormal behavior IEA N RGD:5509061 20181227 MGI 737531 Gde1 glycerophosphodiester phosphodiesterase 1 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20211021 MGI 737531 Gde1 glycerophosphodiester phosphodiesterase 1 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141003 MGI PMID:20393650 737531 Gde1 glycerophosphodiester phosphodiesterase 1 gene MP:0010392 prolonged QRS complex duration IEA N RGD:5509061 20211021 MGI 737531 Gde1 glycerophosphodiester phosphodiesterase 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20201231 MGI 737538 Ednra endothelin receptor type A gene MP:0000022 abnormal ear shape IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0000024 lowered ear position IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20141003 MGI PMID:19185569 737538 Ednra endothelin receptor type A gene MP:0000029 abnormal malleus morphology IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0000088 short mandible IAGP N RGD:5509061 20141003 MGI PMID:19185569 737538 Ednra endothelin receptor type A gene MP:0000088 short mandible IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0000104 abnormal sphenoid bone morphology IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0000106 abnormal basisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0000114 cleft chin IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0000120 malocclusion IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0000266 abnormal heart morphology IAGP N RGD:5509061 20141003 MGI PMID:20929948 737538 Ednra endothelin receptor type A gene MP:0000267 abnormal heart development IAGP N RGD:5509061 20141003 MGI PMID:20929948 737538 Ednra endothelin receptor type A gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0000273 overriding aortic valve IAGP N RGD:5509061 20141003 MGI PMID:9649553 737538 Ednra endothelin receptor type A gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0000284 double outlet right ventricle IAGP N RGD:5509061 20141003 MGI PMID:9649553 737538 Ednra endothelin receptor type A gene MP:0000428 abnormal craniofacial morphology IAGP N RGD:5509061 20141003 MGI PMID:19185569 737538 Ednra endothelin receptor type A gene MP:0000435 shortened head IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0000445 short snout IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0000452 abnormal mouth morphology IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0000454 abnormal jaw morphology IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20141003 MGI PMID:15306564 737538 Ednra endothelin receptor type A gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:15306564 737538 Ednra endothelin receptor type A gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20141003 MGI PMID:19185569 737538 Ednra endothelin receptor type A gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0000460 mandible hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0000614 absent salivary gland IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0001065 abnormal trigeminal nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0001068 abnormal mandibular nerve branching IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0001071 abnormal facial nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0001265 decreased body size IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0001296 macrophthalmia IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0001302 eyelids open at birth IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0001304 cataract IEA N RGD:5509061 20240523 MGI 737538 Ednra endothelin receptor type A gene MP:0001489 decreased startle reflex IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0001787 pericardial edema IAGP N RGD:5509061 20141003 MGI PMID:15664398 737538 Ednra endothelin receptor type A gene MP:0001823 thymus hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0002080 prenatal lethality IAGP N RGD:5509061 20141003 MGI PMID:9449665 737538 Ednra endothelin receptor type A gene MP:0002108 abnormal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0002116 abnormal craniofacial bone morphology IAGP N RGD:5509061 20141003 MGI PMID:19185569 737538 Ednra endothelin receptor type A gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:14585980 737538 Ednra endothelin receptor type A gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:16868309 737538 Ednra endothelin receptor type A gene MP:0002177 abnormal outer ear morphology IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9449665 737538 Ednra endothelin receptor type A gene MP:0002191 abnormal artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9649553 737538 Ednra endothelin receptor type A gene MP:0002309 abnormal vital capacity IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0002311 abnormal inspiratory capacity IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0002338 abnormal pulmonary ventilation IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:15664398 737538 Ednra endothelin receptor type A gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0002633 persistent truncus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:9649553 737538 Ednra endothelin receptor type A gene MP:0002639 micrognathia IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0002672 abnormal pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9649553 737538 Ednra endothelin receptor type A gene MP:0002987 abnormal urine osmolality IAGP N RGD:5509061 20141003 MGI PMID:15928212 737538 Ednra endothelin receptor type A gene MP:0003007 ectopic thymus IAGP N RGD:5509061 20150319 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0003056 abnormal hyoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:15306564 737538 Ednra endothelin receptor type A gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0003139 patent ductus arteriosus IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:15664398 737538 Ednra endothelin receptor type A gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15306564 737538 Ednra endothelin receptor type A gene MP:0003235 abnormal alisphenoid bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0003716 anteriorly rotated ears IAGP N RGD:5509061 20171005 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0003743 abnormal facial morphology IEA N RGD:5509061 20201022 MGI 737538 Ednra endothelin receptor type A gene MP:0003755 abnormal palate morphology IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0004159 double aortic arch IAGP N RGD:5509061 20141003 MGI PMID:9649553 737538 Ednra endothelin receptor type A gene MP:0004181 abnormal carotid artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0004189 abnormal alveolar process morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0004204 absent stapes IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0004235 abnormal masseter muscle morphology IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0004318 absent incus IAGP N RGD:5509061 20141003 MGI PMID:19185569 737538 Ednra endothelin receptor type A gene MP:0004318 absent incus IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0004319 absent malleus IAGP N RGD:5509061 20141003 MGI PMID:19185569 737538 Ednra endothelin receptor type A gene MP:0004319 absent malleus IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20141003 MGI PMID:19185569 737538 Ednra endothelin receptor type A gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0004439 absent Meckel's cartilage IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0004452 abnormal pterygoid process morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0004468 small zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:15306564 737538 Ednra endothelin receptor type A gene MP:0004468 small zygomatic bone IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0004469 abnormal zygomatic arch morphology IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0004595 abnormal mandibular condyloid process morphology IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0004739 conductive hearing loss IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:15664398 737538 Ednra endothelin receptor type A gene MP:0004787 abnormal dorsal aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0004899 absent temporal bone squamous part IAGP N RGD:5509061 20171005 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0005105 abnormal middle ear ossicle morphology IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0005106 abnormal incus morphology IAGP N RGD:5509061 20141003 MGI PMID:19185569 737538 Ednra endothelin receptor type A gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20150702 MGI PMID:19185569 737538 Ednra endothelin receptor type A gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:15306564 737538 Ednra endothelin receptor type A gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20141003 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:20929948 737538 Ednra endothelin receptor type A gene MP:0005312 pericardial effusion IAGP N RGD:5509061 20141003 MGI PMID:9449665 737538 Ednra endothelin receptor type A gene MP:0005358 abnormal incisor morphology IAGP N RGD:5509061 20141003 MGI PMID:19185569 737538 Ednra endothelin receptor type A gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:15306564 737538 Ednra endothelin receptor type A gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0005610 increased circulating antidiuretic hormone level IAGP N RGD:5509061 20141003 MGI PMID:15928212 737538 Ednra endothelin receptor type A gene MP:0006019 absent tympanic membrane IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0006325 impaired hearing IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0006337 abnormal first pharyngeal arch morphology IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0006344 small second pharyngeal arch IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0006354 abnormal fourth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9649553 737538 Ednra endothelin receptor type A gene MP:0006355 abnormal sixth pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9649553 737538 Ednra endothelin receptor type A gene MP:0006356 abnormal third pharyngeal arch artery morphology IAGP N RGD:5509061 20141003 MGI PMID:9649553 737538 Ednra endothelin receptor type A gene MP:0008023 abnormal styloid process morphology IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0008380 abnormal gonial bone morphology IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0008381 absent gonial bone IAGP N RGD:5509061 20141003 MGI PMID:15306564 737538 Ednra endothelin receptor type A gene MP:0008381 absent gonial bone IAGP N RGD:5509061 20141003 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0008381 absent gonial bone IAGP N RGD:5509061 20171005 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0008797 facial cleft IAGP N RGD:5509061 20141003 MGI PMID:19185569 737538 Ednra endothelin receptor type A gene MP:0009142 decreased prepulse inhibition IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0009524 absent submandibular gland IAGP N RGD:5509061 20150101 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0009800 abnormal mandibular nerve morphology IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0009867 abnormal ascending aorta morphology IAGP N RGD:5509061 20141003 MGI PMID:9649553 737538 Ednra endothelin receptor type A gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:19185569 737538 Ednra endothelin receptor type A gene MP:0009904 tongue hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0010030 abnormal orbit morphology IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0010150 abnormal mandibular ramus morphology IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0010418 perimembraneous ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0010465 aberrant origin of the right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:9649553 737538 Ednra endothelin receptor type A gene MP:0010486 absent right subclavian artery IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0010543 aorta tubular hypoplasia IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0010544 interrupted aorta IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0010572 persistent right dorsal aorta IAGP N RGD:5509061 20141003 MGI PMID:9649553 737538 Ednra endothelin receptor type A gene MP:0010896 decreased lung compliance IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0010938 decreased total lung capacity IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0011089 perinatal lethality, complete penetrance IAGP N RGD:5509061 20151119 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737538 Ednra endothelin receptor type A gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15664398 737538 Ednra endothelin receptor type A gene MP:0011210 abnormal temporomandibular joint morphology IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0011665 d-loop transposition of the great arteries IAGP N RGD:5509061 20240118 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20170126 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0013262 abnormal mouth floor morphology IAGP N RGD:5509061 20150702 MGI PMID:15306564 737538 Ednra endothelin receptor type A gene MP:0013262 abnormal mouth floor morphology IAGP N RGD:5509061 20150702 MGI PMID:19185569 737538 Ednra endothelin receptor type A gene MP:0013917 persistent right 6th pharyngeal arch artery IAGP N RGD:5509061 20191219 MGI PMID:9649553 737538 Ednra endothelin receptor type A gene MP:0030072 round face IAGP N RGD:5509061 20170928 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0030092 abnormal outer ear helix morphology IAGP N RGD:5509061 20170928 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0030104 round orbits IAGP N RGD:5509061 20170928 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0030109 abnormal incudomalleolar joint morphology IAGP N RGD:5509061 20171207 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0030110 incudomalleolar fusion IAGP N RGD:5509061 20171005 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0030228 absent tubotympanic recess IAGP N RGD:5509061 20171019 MGI PMID:9449664 737538 Ednra endothelin receptor type A gene MP:0030247 prominent cheeks IAGP N RGD:5509061 20171019 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0030258 small mandibular condyloid process IAGP N RGD:5509061 20171019 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0030261 abnormal temporal bone zygomatic process morphology IAGP N RGD:5509061 20171207 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0030261 abnormal temporal bone zygomatic process morphology IAGP N RGD:5509061 20171214 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0030284 short mandibular coronoid process IAGP N RGD:5509061 20171102 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0030299 lower jaw to upper jaw transformation IAGP N RGD:5509061 20171102 MGI PMID:15306564 737538 Ednra endothelin receptor type A gene MP:0030299 lower jaw to upper jaw transformation IAGP N RGD:5509061 20171102 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0030300 upper jaw to lower jaw transformation IAGP N RGD:5509061 20171102 MGI PMID:19017795 737538 Ednra endothelin receptor type A gene MP:0030319 abnormal temporal bone petrous part morphology IAGP N RGD:5509061 20171109 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0030323 short styloid process IAGP N RGD:5509061 20171109 MGI PMID:18199583 737538 Ednra endothelin receptor type A gene MP:0030351 wide coronal suture IAGP N RGD:5509061 20171116 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0030353 wide sagittal suture IAGP N RGD:5509061 20171116 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0030357 wide lambdoid suture IAGP N RGD:5509061 20171116 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0030395 absent incus short process IAGP N RGD:5509061 20171207 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0030416 absent temporal bone zygomatic process IAGP N RGD:5509061 20171207 MGI PMID:27671791 737538 Ednra endothelin receptor type A gene MP:0030416 absent temporal bone zygomatic process IAGP N RGD:5509061 20171214 MGI PMID:18199583 737540 Fkbp1a FK506 binding protein 1a gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:23571217 737540 Fkbp1a FK506 binding protein 1a gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21803290 737540 Fkbp1a FK506 binding protein 1a gene MP:0000914 exencephaly IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0000929 open neural tube IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:15289441 737540 Fkbp1a FK506 binding protein 1a gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:23571217 737540 Fkbp1a FK506 binding protein 1a gene MP:0001654 hepatic necrosis IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23571217 737540 Fkbp1a FK506 binding protein 1a gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23571217 737540 Fkbp1a FK506 binding protein 1a gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:15289441 737540 Fkbp1a FK506 binding protein 1a gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:21803290 737540 Fkbp1a FK506 binding protein 1a gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20141003 MGI 737540 Fkbp1a FK506 binding protein 1a gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0002754 dilated heart right ventricle IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0002795 dilated cardiomyopathy IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0002833 increased heart weight IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:15289441 737540 Fkbp1a FK506 binding protein 1a gene MP:0003140 dilated heart atrium IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0003674 oxidative stress IAGP N RGD:5509061 20141003 MGI PMID:21803290 737540 Fkbp1a FK506 binding protein 1a gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0003888 liver hemorrhage IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0004032 abnormal interventricular groove morphology IAGP N RGD:5509061 20141003 MGI PMID:23571217 737540 Fkbp1a FK506 binding protein 1a gene MP:0004067 abnormal trabecula carnea morphology IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0004215 abnormal myocardial fiber physiology IAGP N RGD:5509061 20141003 MGI PMID:21372286 737540 Fkbp1a FK506 binding protein 1a gene MP:0004231 abnormal calcium ion homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15289441 737540 Fkbp1a FK506 binding protein 1a gene MP:0004937 dilated heart IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0005294 abnormal heart ventricle morphology IAGP N RGD:5509061 20141003 MGI PMID:23571217 737540 Fkbp1a FK506 binding protein 1a gene MP:0005329 abnormal myocardium layer morphology IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0005598 decreased heart ventricle muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:15289441 737540 Fkbp1a FK506 binding protein 1a gene MP:0005620 abnormal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:21803290 737540 Fkbp1a FK506 binding protein 1a gene MP:0006138 congestive heart failure IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0009404 centrally nucleated skeletal muscle fibers IAGP N RGD:5509061 20141003 MGI PMID:15289441 737540 Fkbp1a FK506 binding protein 1a gene MP:0009409 abnormal skeletal muscle fiber type ratio IAGP N RGD:5509061 20141003 MGI PMID:15289441 737540 Fkbp1a FK506 binding protein 1a gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:23571217 737540 Fkbp1a FK506 binding protein 1a gene MP:0010402 ventricular septal defect IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0010508 abnormal heart electrocardiography waveform feature IAGP N RGD:5509061 20141003 MGI PMID:21372286 737540 Fkbp1a FK506 binding protein 1a gene MP:0010556 thin ventricle myocardium compact layer IAGP N RGD:5509061 20141003 MGI PMID:23571217 737540 Fkbp1a FK506 binding protein 1a gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0011099 lethality throughout fetal growth and development, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23571217 737540 Fkbp1a FK506 binding protein 1a gene MP:0011109 lethality throughout fetal growth and development, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9461216 737540 Fkbp1a FK506 binding protein 1a gene MP:0012106 impaired exercise endurance IAGP N RGD:5509061 20141003 MGI PMID:21803290 737540 Fkbp1a FK506 binding protein 1a gene MP:0021158 decreased heart left ventricle wall thickness IAGP N RGD:5509061 20231109 MGI PMID:9461216 737543 Sdr9c7 4short chain dehydrogenase/reductase family 9C, member 7 gene MP:0001222 epidermal hyperplasia IAGP N RGD:5509061 20201112 MGI PMID:31671075 737543 Sdr9c7 4short chain dehydrogenase/reductase family 9C, member 7 gene MP:0001240 abnormal epidermis stratum corneum morphology IAGP N RGD:5509061 20201112 MGI PMID:31671075 737543 Sdr9c7 4short chain dehydrogenase/reductase family 9C, member 7 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20201112 MGI PMID:31671075 737543 Sdr9c7 4short chain dehydrogenase/reductase family 9C, member 7 gene MP:0001263 weight loss IAGP N RGD:5509061 20201112 MGI PMID:31671075 737543 Sdr9c7 4short chain dehydrogenase/reductase family 9C, member 7 gene MP:0002796 impaired skin barrier function IAGP N RGD:5509061 20201112 MGI PMID:31671075 737543 Sdr9c7 4short chain dehydrogenase/reductase family 9C, member 7 gene MP:0003853 dry skin IAGP N RGD:5509061 20201112 MGI PMID:31671075 737543 Sdr9c7 4short chain dehydrogenase/reductase family 9C, member 7 gene MP:0009594 abnormal corneocyte envelope morphology IAGP N RGD:5509061 20201112 MGI PMID:31671075 737543 Sdr9c7 4short chain dehydrogenase/reductase family 9C, member 7 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20201112 MGI PMID:31671075 737543 Sdr9c7 4short chain dehydrogenase/reductase family 9C, member 7 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20240523 MGI 737545 Hcrtr1 hypocretin (orexin) receptor 1 gene MP:0002556 abnormal cocaine consumption IAGP N RGD:5509061 20150129 MGI PMID:22837742 737545 Hcrtr1 hypocretin (orexin) receptor 1 gene MP:0002556 abnormal cocaine consumption IAGP N RGD:5509061 20150129 MGI PMID:24706819 737545 Hcrtr1 hypocretin (orexin) receptor 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IEA N RGD:5509061 20111116 MGI 737545 Hcrtr1 hypocretin (orexin) receptor 1 gene MP:0003360 abnormal depression-related behavior IAGP N RGD:5509061 20141003 MGI PMID:21377495 737545 Hcrtr1 hypocretin (orexin) receptor 1 gene MP:0012341 low preference for an addictive substance IAGP N RGD:5509061 20150129 MGI PMID:22837742 737545 Hcrtr1 hypocretin (orexin) receptor 1 gene MP:0012341 low preference for an addictive substance IAGP N RGD:5509061 20150129 MGI PMID:24706819 737547 Cbr1 carbonyl reductase 1 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20210617 MGI PMID:32843708 737547 Cbr1 carbonyl reductase 1 gene MP:0002272 abnormal nervous system electrophysiology IAGP N RGD:5509061 20210617 MGI PMID:32843708 737547 Cbr1 carbonyl reductase 1 gene MP:0003908 decreased stereotypic behavior IAGP N RGD:5509061 20210617 MGI PMID:32843708 737547 Cbr1 carbonyl reductase 1 gene MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:32843708 737549 Edn2 endothelin 2 gene MP:0000255 blood vessel congestion IAGP N RGD:5509061 20220609 MGI PMID:24763822 737549 Edn2 endothelin 2 gene MP:0000746 weakness IAGP N RGD:5509061 20220609 MGI PMID:24763822 737549 Edn2 endothelin 2 gene MP:0001127 small ovary IAGP N RGD:5509061 20220609 MGI PMID:24763822 737549 Edn2 endothelin 2 gene MP:0001133 impaired luteal cell differentiation IAGP N RGD:5509061 20220609 MGI PMID:24763822 737549 Edn2 endothelin 2 gene MP:0001134 absent corpus luteum IAGP N RGD:5509061 20220609 MGI PMID:24763822 737549 Edn2 endothelin 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:24043815 737549 Edn2 endothelin 2 gene MP:0001265 decreased body size IAGP N RGD:5509061 20220609 MGI PMID:24763822 737549 Edn2 endothelin 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0002083 premature death IAGP N RGD:5509061 20220609 MGI PMID:24763822 737549 Edn2 endothelin 2 gene MP:0002270 abnormal pulmonary alveolus morphology IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0002318 hypercapnia IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0002575 increased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0002608 increased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0002637 small uterus IAGP N RGD:5509061 20220609 MGI PMID:24763822 737549 Edn2 endothelin 2 gene MP:0002971 abnormal brown adipose tissue morphology IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0003016 increased circulating bicarbonate level IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0003030 acidemia IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0003031 acidosis IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0003948 abnormal gas homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0005039 hypoxia IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0005185 decreased circulating progesterone level IAGP N RGD:5509061 20220609 MGI PMID:24763822 737549 Edn2 endothelin 2 gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0005534 decreased body temperature IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0005565 increased blood urea nitrogen level IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0008032 abnormal lipolysis IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20220609 MGI PMID:24763822 737549 Edn2 endothelin 2 gene MP:0008821 increased blood uric acid level IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0009642 abnormal blood homeostasis IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0010902 abnormal pulmonary alveolar sac morphology IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0010937 increased total lung capacity IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0011049 impaired adaptive thermogenesis IAGP N RGD:5509061 20151001 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24043815 737549 Edn2 endothelin 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737549 Edn2 endothelin 2 gene MP:0011285 increased circulating erythropoietin level IAGP N RGD:5509061 20141003 MGI PMID:23676500 737549 Edn2 endothelin 2 gene MP:0013609 abnormal ovarian medulla morphology IAGP N RGD:5509061 20220609 MGI PMID:24763822 737549 Edn2 endothelin 2 gene MP:0031420 decreased superovulation rate IAGP N RGD:5509061 20220630 MGI PMID:24763822 737551 Grm3 glutamate receptor, metabotropic 3 gene MP:0001297 microphthalmia IEA N RGD:5509061 20181227 MGI 737551 Grm3 glutamate receptor, metabotropic 3 gene MP:0001362 abnormal anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:15619115 737551 Grm3 glutamate receptor, metabotropic 3 gene MP:0001552 increased circulating triglyceride level IEA N RGD:5509061 20210128 MGI 737551 Grm3 glutamate receptor, metabotropic 3 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20201022 MGI 737551 Grm3 glutamate receptor, metabotropic 3 gene MP:0002169 no abnormal phenotype detected IEA N RGD:5509061 20111116 MGI 737551 Grm3 glutamate receptor, metabotropic 3 gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20211021 MGI 737551 Grm3 glutamate receptor, metabotropic 3 gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20211021 MGI 737551 Grm3 glutamate receptor, metabotropic 3 gene MP:0004811 abnormal neuron physiology IAGP N RGD:5509061 20141003 MGI PMID:24053122 737551 Grm3 glutamate receptor, metabotropic 3 gene MP:0005178 increased circulating cholesterol level IEA N RGD:5509061 20160421 MGI 737551 Grm3 glutamate receptor, metabotropic 3 gene MP:0005293 impaired glucose tolerance IEA N RGD:5509061 20211021 MGI 737551 Grm3 glutamate receptor, metabotropic 3 gene MP:0008916 abnormal astrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:24053122 737551 Grm3 glutamate receptor, metabotropic 3 gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20211021 MGI 737551 Grm3 glutamate receptor, metabotropic 3 gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20201022 MGI 737552 Fbxo32 F-box protein 32 gene MP:0004064 decreased susceptibility to induced muscular atrophy IAGP N RGD:5509061 20151203 MGI PMID:11679633 737557 Thrb thyroid hormone receptor beta gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:12382103 737557 Thrb thyroid hormone receptor beta gene MP:0000031 abnormal cochlea morphology IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:11739587 737557 Thrb thyroid hormone receptor beta gene MP:0000042 abnormal organ of Corti morphology IAGP N RGD:5509061 20141003 MGI PMID:12382103 737557 Thrb thyroid hormone receptor beta gene MP:0000043 organ of Corti degeneration IAGP N RGD:5509061 20141003 MGI PMID:12382103 737557 Thrb thyroid hormone receptor beta gene MP:0000066 osteoporosis IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0000081 premature cranial suture closure IAGP N RGD:5509061 20141003 MGI PMID:16051666 737557 Thrb thyroid hormone receptor beta gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0000135 decreased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20141003 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0000478 delayed intestine development IAGP N RGD:5509061 20141003 MGI PMID:9927422 737557 Thrb thyroid hormone receptor beta gene MP:0000496 abnormal small intestine morphology IAGP N RGD:5509061 20141003 MGI PMID:9927422 737557 Thrb thyroid hormone receptor beta gene MP:0000547 short limbs IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0000636 enlarged pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:15601836 737557 Thrb thyroid hormone receptor beta gene MP:0000745 tremors IEA N RGD:5509061 20141003 MGI 737557 Thrb thyroid hormone receptor beta gene MP:0000852 small cerebellum IAGP N RGD:5509061 20141003 MGI PMID:11274423 737557 Thrb thyroid hormone receptor beta gene MP:0000875 abnormal cerebellar Purkinje cell layer IAGP N RGD:5509061 20141003 MGI PMID:11274423 737557 Thrb thyroid hormone receptor beta gene MP:0000877 abnormal Purkinje cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11274423 737557 Thrb thyroid hormone receptor beta gene MP:0000880 decreased Purkinje cell number IAGP N RGD:5509061 20141003 MGI PMID:11274423 737557 Thrb thyroid hormone receptor beta gene MP:0000890 thin cerebellar molecular layer IAGP N RGD:5509061 20141003 MGI PMID:11274423 737557 Thrb thyroid hormone receptor beta gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11138006 737557 Thrb thyroid hormone receptor beta gene MP:0001006 abnormal retina cone cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12356724 737557 Thrb thyroid hormone receptor beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17210747 737557 Thrb thyroid hormone receptor beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:9927422 737557 Thrb thyroid hormone receptor beta gene MP:0001262 decreased body weight IAGP N RGD:5509061 20170803 MGI PMID:19439650 737557 Thrb thyroid hormone receptor beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11069286 737557 Thrb thyroid hormone receptor beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:11739587 737557 Thrb thyroid hormone receptor beta gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:15983791 737557 Thrb thyroid hormone receptor beta gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:11274423 737557 Thrb thyroid hormone receptor beta gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20160929 MGI PMID:24932806 737557 Thrb thyroid hormone receptor beta gene MP:0001496 audiogenic seizures IAGP N RGD:5509061 20141003 MGI PMID:11496110 737557 Thrb thyroid hormone receptor beta gene MP:0001541 abnormal osteoclast physiology IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0001731 abnormal postnatal growth IAGP N RGD:5509061 20141003 MGI PMID:12356724 737557 Thrb thyroid hormone receptor beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11069286 737557 Thrb thyroid hormone receptor beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:11726557 737557 Thrb thyroid hormone receptor beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:9927422 737557 Thrb thyroid hormone receptor beta gene MP:0001900 impaired synaptic plasticity IAGP N RGD:5509061 20160929 MGI PMID:24932806 737557 Thrb thyroid hormone receptor beta gene MP:0001926 female infertility IAGP N RGD:5509061 20141003 MGI PMID:11739587 737557 Thrb thyroid hormone receptor beta gene MP:0001954 respiratory distress IAGP N RGD:5509061 20141003 MGI PMID:15231697 737557 Thrb thyroid hormone receptor beta gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:11496110 737557 Thrb thyroid hormone receptor beta gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:8673137 737557 Thrb thyroid hormone receptor beta gene MP:0002041 increased pituitary adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15601836 737557 Thrb thyroid hormone receptor beta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:15231697 737557 Thrb thyroid hormone receptor beta gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:9927422 737557 Thrb thyroid hormone receptor beta gene MP:0002109 abnormal limb morphology IAGP N RGD:5509061 20141003 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0002113 abnormal skeleton development IAGP N RGD:5509061 20141003 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0002626 increased heart rate IAGP N RGD:5509061 20141003 MGI PMID:11159823 737557 Thrb thyroid hormone receptor beta gene MP:0002674 abnormal sperm motility IAGP N RGD:5509061 20141003 MGI PMID:17210747 737557 Thrb thyroid hormone receptor beta gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:15983791 737557 Thrb thyroid hormone receptor beta gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:11069286 737557 Thrb thyroid hormone receptor beta gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:16051666 737557 Thrb thyroid hormone receptor beta gene MP:0002764 short tibia IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0002874 decreased hemoglobin content IEA N RGD:5509061 20141003 MGI 737557 Thrb thyroid hormone receptor beta gene MP:0002876 abnormal thyroid gland physiology IAGP N RGD:5509061 20141003 MGI PMID:10430610 737557 Thrb thyroid hormone receptor beta gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0002896 abnormal bone mineralization IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0003055 abnormal long bone epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:9927422 737557 Thrb thyroid hormone receptor beta gene MP:0003109 short femur IAGP N RGD:5509061 20141003 MGI PMID:11069286 737557 Thrb thyroid hormone receptor beta gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:11739587 737557 Thrb thyroid hormone receptor beta gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12382103 737557 Thrb thyroid hormone receptor beta gene MP:0003149 abnormal tectorial membrane morphology IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0003150 detached tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:12382103 737557 Thrb thyroid hormone receptor beta gene MP:0003350 increased circulating levels of thyroid hormone IAGP N RGD:5509061 20141003 MGI PMID:24265449 737557 Thrb thyroid hormone receptor beta gene MP:0003417 premature endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0003417 premature endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16051666 737557 Thrb thyroid hormone receptor beta gene MP:0003417 premature endochondral bone ossification IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0003418 premature intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0003418 premature intramembranous bone ossification IAGP N RGD:5509061 20141003 MGI PMID:16051666 737557 Thrb thyroid hormone receptor beta gene MP:0003442 decreased circulating glycerol level IEA N RGD:5509061 20141003 MGI 737557 Thrb thyroid hormone receptor beta gene MP:0003498 thyroid gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:11069286 737557 Thrb thyroid hormone receptor beta gene MP:0003498 thyroid gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:8670802 737557 Thrb thyroid hormone receptor beta gene MP:0003498 thyroid gland hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:9927422 737557 Thrb thyroid hormone receptor beta gene MP:0003502 increased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0003502 increased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0003502 increased activity of thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:8670802 737557 Thrb thyroid hormone receptor beta gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:12576486 737557 Thrb thyroid hormone receptor beta gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0003638 abnormal response/metabolism to endogenous compounds IAGP N RGD:5509061 20160128 MGI PMID:25774556 737557 Thrb thyroid hormone receptor beta gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0003795 abnormal bone structure IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:11739587 737557 Thrb thyroid hormone receptor beta gene MP:0003825 abnormal pillar cell morphology IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0003965 abnormal pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:15601836 737557 Thrb thyroid hormone receptor beta gene MP:0003965 abnormal pituitary hormone level IAGP N RGD:5509061 20141003 MGI PMID:17210747 737557 Thrb thyroid hormone receptor beta gene MP:0004022 abnormal cone electrophysiology IAGP N RGD:5509061 20141003 MGI PMID:11138006 737557 Thrb thyroid hormone receptor beta gene MP:0004148 increased compact bone thickness IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0004197 abnormal fetal growth/weight/body size IAGP N RGD:5509061 20141003 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0004362 cochlear hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12382103 737557 Thrb thyroid hormone receptor beta gene MP:0004402 decreased cochlear outer hair cell number IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:11739587 737557 Thrb thyroid hormone receptor beta gene MP:0004414 decreased cochlear microphonics IAGP N RGD:5509061 20141003 MGI PMID:19244534 737557 Thrb thyroid hormone receptor beta gene MP:0004415 abnormal cochlear nerve compound action potential IAGP N RGD:5509061 20141003 MGI PMID:19244534 737557 Thrb thyroid hormone receptor beta gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11726557 737557 Thrb thyroid hormone receptor beta gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11739587 737557 Thrb thyroid hormone receptor beta gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:19244534 737557 Thrb thyroid hormone receptor beta gene MP:0004433 abnormal cochlear inner hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:9861043 737557 Thrb thyroid hormone receptor beta gene MP:0004434 abnormal cochlear outer hair cell physiology IAGP N RGD:5509061 20141003 MGI PMID:11739587 737557 Thrb thyroid hormone receptor beta gene MP:0004437 decreased cochlear outer hair cell electromotility IAGP N RGD:5509061 20141003 MGI PMID:11739587 737557 Thrb thyroid hormone receptor beta gene MP:0004437 decreased cochlear outer hair cell electromotility IAGP N RGD:5509061 20141003 MGI PMID:9861043 737557 Thrb thyroid hormone receptor beta gene MP:0004465 degeneration of organ of Corti supporting cells IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0004466 short cochlear outer hair cells IAGP N RGD:5509061 20141003 MGI PMID:9861043 737557 Thrb thyroid hormone receptor beta gene MP:0004591 enlarged tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:11739587 737557 Thrb thyroid hormone receptor beta gene MP:0004591 enlarged tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:12382103 737557 Thrb thyroid hormone receptor beta gene MP:0004591 enlarged tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0004591 enlarged tectorial membrane IAGP N RGD:5509061 20141003 MGI PMID:19244534 737557 Thrb thyroid hormone receptor beta gene MP:0004664 delayed inner ear development IAGP N RGD:5509061 20141003 MGI PMID:11739587 737557 Thrb thyroid hormone receptor beta gene MP:0004664 delayed inner ear development IAGP N RGD:5509061 20141003 MGI PMID:8673137 737557 Thrb thyroid hormone receptor beta gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11069286 737557 Thrb thyroid hormone receptor beta gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11726557 737557 Thrb thyroid hormone receptor beta gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:8670802 737557 Thrb thyroid hormone receptor beta gene MP:0004696 abnormal thyroid follicle morphology IAGP N RGD:5509061 20141003 MGI PMID:9927422 737557 Thrb thyroid hormone receptor beta gene MP:0004701 decreased circulating insulin-like growth factor I level IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0004737 absent distortion product otoacoustic emissions IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0004738 abnormal auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11739587 737557 Thrb thyroid hormone receptor beta gene MP:0004740 sensorineural hearing loss IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20141003 MGI PMID:17210747 737557 Thrb thyroid hormone receptor beta gene MP:0004864 spiral ligament degeneration IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0004984 increased osteoclast cell number IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0005119 decreased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:24265449 737557 Thrb thyroid hormone receptor beta gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:10430610 737557 Thrb thyroid hormone receptor beta gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11069286 737557 Thrb thyroid hormone receptor beta gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11138006 737557 Thrb thyroid hormone receptor beta gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11274423 737557 Thrb thyroid hormone receptor beta gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12576486 737557 Thrb thyroid hormone receptor beta gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:15601836 737557 Thrb thyroid hormone receptor beta gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:16100573 737557 Thrb thyroid hormone receptor beta gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0005122 increased circulating thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:9927422 737557 Thrb thyroid hormone receptor beta gene MP:0005130 decreased follicle stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17210747 737557 Thrb thyroid hormone receptor beta gene MP:0005132 decreased luteinizing hormone level IAGP N RGD:5509061 20141003 MGI PMID:17210747 737557 Thrb thyroid hormone receptor beta gene MP:0005135 increased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11496110 737557 Thrb thyroid hormone receptor beta gene MP:0005135 increased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:17210747 737557 Thrb thyroid hormone receptor beta gene MP:0005135 increased thyroid-stimulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:8670802 737557 Thrb thyroid hormone receptor beta gene MP:0005136 decreased growth hormone level IAGP N RGD:5509061 20141003 MGI PMID:17210747 737557 Thrb thyroid hormone receptor beta gene MP:0005138 decreased prolactin level IAGP N RGD:5509061 20141003 MGI PMID:17210747 737557 Thrb thyroid hormone receptor beta gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:11069286 737557 Thrb thyroid hormone receptor beta gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:15231697 737557 Thrb thyroid hormone receptor beta gene MP:0005355 enlarged thyroid gland IAGP N RGD:5509061 20141003 MGI PMID:8670802 737557 Thrb thyroid hormone receptor beta gene MP:0005361 small pituitary gland IAGP N RGD:5509061 20141003 MGI PMID:15601836 737557 Thrb thyroid hormone receptor beta gene MP:0005418 abnormal circulating hormone level IAGP N RGD:5509061 20141003 MGI PMID:11069286 737557 Thrb thyroid hormone receptor beta gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:11726557 737557 Thrb thyroid hormone receptor beta gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:15601836 737557 Thrb thyroid hormone receptor beta gene MP:0005468 abnormal thyroid hormone level IAGP N RGD:5509061 20141003 MGI PMID:24265449 737557 Thrb thyroid hormone receptor beta gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:10430610 737557 Thrb thyroid hormone receptor beta gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:11274423 737557 Thrb thyroid hormone receptor beta gene MP:0005470 increased thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:24265449 737557 Thrb thyroid hormone receptor beta gene MP:0005474 increased triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:10430610 737557 Thrb thyroid hormone receptor beta gene MP:0005474 increased triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:11274423 737557 Thrb thyroid hormone receptor beta gene MP:0005474 increased triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:9927422 737557 Thrb thyroid hormone receptor beta gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:11069286 737557 Thrb thyroid hormone receptor beta gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:11159823 737557 Thrb thyroid hormone receptor beta gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:11496110 737557 Thrb thyroid hormone receptor beta gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:12576486 737557 Thrb thyroid hormone receptor beta gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:15601836 737557 Thrb thyroid hormone receptor beta gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:16100573 737557 Thrb thyroid hormone receptor beta gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:19439650 737557 Thrb thyroid hormone receptor beta gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:24265449 737557 Thrb thyroid hormone receptor beta gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:8670802 737557 Thrb thyroid hormone receptor beta gene MP:0005477 increased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:9927422 737557 Thrb thyroid hormone receptor beta gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:11726557 737557 Thrb thyroid hormone receptor beta gene MP:0005478 decreased circulating thyroxine level IAGP N RGD:5509061 20141003 MGI PMID:8670802 737557 Thrb thyroid hormone receptor beta gene MP:0005479 decreased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:11726557 737557 Thrb thyroid hormone receptor beta gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:11069286 737557 Thrb thyroid hormone receptor beta gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:11138006 737557 Thrb thyroid hormone receptor beta gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:11496110 737557 Thrb thyroid hormone receptor beta gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:12576486 737557 Thrb thyroid hormone receptor beta gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:15601836 737557 Thrb thyroid hormone receptor beta gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:16100573 737557 Thrb thyroid hormone receptor beta gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:19439650 737557 Thrb thyroid hormone receptor beta gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:8670802 737557 Thrb thyroid hormone receptor beta gene MP:0005480 increased circulating triiodothyronine level IAGP N RGD:5509061 20141003 MGI PMID:9927422 737557 Thrb thyroid hormone receptor beta gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:11069286 737557 Thrb thyroid hormone receptor beta gene MP:0005646 abnormal pituitary gland physiology IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0006325 impaired hearing IAGP N RGD:5509061 20141003 MGI PMID:12382103 737557 Thrb thyroid hormone receptor beta gene MP:0006395 abnormal epiphyseal plate morphology IAGP N RGD:5509061 20141003 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0006396 decreased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0008142 decreased small intestinal villus size IAGP N RGD:5509061 20141003 MGI PMID:9927422 737557 Thrb thyroid hormone receptor beta gene MP:0008337 increased thyrotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:11069286 737557 Thrb thyroid hormone receptor beta gene MP:0008337 increased thyrotroph cell number IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0009346 decreased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:17327419 737557 Thrb thyroid hormone receptor beta gene MP:0009766 increased susceptibility to xenobiotic induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:11739587 737557 Thrb thyroid hormone receptor beta gene MP:0009780 abnormal chondrocyte physiology IAGP N RGD:5509061 20141003 MGI PMID:17065405 737557 Thrb thyroid hormone receptor beta gene MP:0010346 increased thyroid carcinoma incidence IAGP N RGD:5509061 20141003 MGI PMID:15231697 737557 Thrb thyroid hormone receptor beta gene MP:0011100 preweaning lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12356724 737557 Thrb thyroid hormone receptor beta gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20160929 MGI PMID:24932806 737557 Thrb thyroid hormone receptor beta gene MP:0011617 abnormal habituation IAGP N RGD:5509061 20141003 MGI PMID:15983791 737557 Thrb thyroid hormone receptor beta gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11496110 737557 Thrb thyroid hormone receptor beta gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11726557 737557 Thrb thyroid hormone receptor beta gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:11739587 737557 Thrb thyroid hormone receptor beta gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12382103 737557 Thrb thyroid hormone receptor beta gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:19244534 737557 Thrb thyroid hormone receptor beta gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:8673137 737557 Thrb thyroid hormone receptor beta gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:9861043 737557 Thrb thyroid hormone receptor beta gene MP:0012315 impaired learning IAGP N RGD:5509061 20141003 MGI PMID:15983791 737557 Thrb thyroid hormone receptor beta gene MP:0014091 abnormal tectorial membrane striated-sheet matrix morphology IAGP N RGD:5509061 20160421 MGI PMID:11739587 737557 Thrb thyroid hormone receptor beta gene MP:0014296 delayed skeletal maturation IAGP N RGD:5509061 20230824 MGI PMID:9927422 737557 Thrb thyroid hormone receptor beta gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:12925699 737557 Thrb thyroid hormone receptor beta gene MP:0014406 increased or absent distortion product otoacoustic emission threshold IAGP N RGD:5509061 20240405 MGI PMID:19244534 737557 Thrb thyroid hormone receptor beta gene MP:0020168 decreased thyroid gland weight IAGP N RGD:5509061 20141003 MGI PMID:24265449 737557 Thrb thyroid hormone receptor beta gene MP:0020169 increased thyroid gland weight IAGP N RGD:5509061 20141003 MGI PMID:15231697 737557 Thrb thyroid hormone receptor beta gene MP:0020169 increased thyroid gland weight IAGP N RGD:5509061 20141003 MGI PMID:16100573 737557 Thrb thyroid hormone receptor beta gene MP:0030018 increased cardiac muscle cell glucose uptake IAGP N RGD:5509061 20170803 MGI PMID:15304375 737557 Thrb thyroid hormone receptor beta gene MP:0030389 small fontanelles IAGP N RGD:5509061 20171207 MGI PMID:12677005 737557 Thrb thyroid hormone receptor beta gene MP:0030389 small fontanelles IAGP N RGD:5509061 20171207 MGI PMID:17327419 737558 Pdzk1 PDZ domain containing 1 gene MP:0000182 increased circulating LDL cholesterol level IEA N RGD:5509061 20221027 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0000562 polydactyly IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0000598 abnormal liver morphology IAGP N RGD:5509061 20141003 MGI PMID:15994332 737558 Pdzk1 PDZ domain containing 1 gene MP:0000783 abnormal forebrain morphology IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0001556 increased circulating HDL cholesterol level IEA N RGD:5509061 20221027 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0001879 abnormal lymphatic vessel morphology IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0003686 abnormal eye muscle morphology IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0003826 abnormal Mullerian duct morphology IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0003827 abnormal Wolffian duct morphology IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0005178 increased circulating cholesterol level IAGP N RGD:5509061 20141003 MGI PMID:12556478 737558 Pdzk1 PDZ domain containing 1 gene MP:0005416 abnormal circulating protein level IAGP N RGD:5509061 20141003 MGI PMID:15994332 737558 Pdzk1 PDZ domain containing 1 gene MP:0010404 ostium primum atrial septal defect IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0010412 atrioventricular septal defect IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0010440 anomalous pulmonary venous connection IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20221027 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0013840 absent segment of posterior cerebral artery IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0013848 subcutaneous edema IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0013859 abnormal vitelline vein connection IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0013967 abnormal infrahyoid muscle connection IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0013970 absent connection between subcutaneous lymph vessels and lymph sac IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0013971 blood in lymph vessels IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0013977 symmetric azygos veins IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0013981 double lumen aortic arch IEA N RGD:5509061 20170504 MGI 737558 Pdzk1 PDZ domain containing 1 gene MP:0014001 abnormal vertebral artery topology IEA N RGD:5509061 20170504 MGI 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0000111 cleft palate IAGP N RGD:5509061 20201112 MGI PMID:24554717 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0000762 abnormal tongue morphology IAGP N RGD:5509061 20201112 MGI PMID:24554717 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0000914 exencephaly IAGP N RGD:5509061 20201112 MGI PMID:24554717 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17460611 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0001399 hyperactivity IAGP N RGD:5509061 20201112 MGI PMID:24554717 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0002064 seizures IAGP N RGD:5509061 20201112 MGI PMID:24554717 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0002083 premature death IAGP N RGD:5509061 20201112 MGI PMID:24554717 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20201112 MGI PMID:24554717 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0002574 increased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:17460611 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0002906 increased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:17460611 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0004200 decreased fetal size IAGP N RGD:5509061 20201112 MGI PMID:24554717 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20201112 MGI PMID:24554717 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20201112 MGI PMID:24554717 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0008146 asymmetric sternocostal joints IAGP N RGD:5509061 20201112 MGI PMID:24554717 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0009849 increased vertical stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:17460611 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0011090 perinatal lethality, incomplete penetrance IAGP N RGD:5509061 20201112 MGI PMID:24554717 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:17460611 737560 Impa1 inositol (myo)-1(or 4)-monophosphatase 1 gene MP:0020469 prolonged circadian behavior period IAGP N RGD:5509061 20201112 MGI PMID:24554717 737561 Sfmbt1 Scm-like with four mbt domains 1 gene MP:0011110 preweaning lethality, incomplete penetrance IEA N RGD:5509061 20220811 MGI 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0001147 small testis IAGP N RGD:5509061 20230330 MGI PMID:36398584 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21990309 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0001552 increased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:21990309 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0001554 increased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:21990309 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0001777 abnormal body temperature homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21990309 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20230330 MGI PMID:36398584 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0002078 abnormal glucose homeostasis IAGP N RGD:5509061 20141003 MGI PMID:20670938 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:20670938 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:21990309 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0002118 abnormal lipid homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21990309 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20230330 MGI PMID:36398584 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20230330 MGI PMID:36398584 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0003058 increased insulin secretion IAGP N RGD:5509061 20141003 MGI PMID:21990309 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0003458 decreased circulating ketone body level IAGP N RGD:5509061 20141003 MGI PMID:21990309 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0004852 decreased testis weight IAGP N RGD:5509061 20230330 MGI PMID:36398584 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20230330 MGI PMID:36398584 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0005216 abnormal pancreatic alpha cell morphology IAGP N RGD:5509061 20141003 MGI PMID:20670938 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0005280 abnormal fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:20670938 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0005281 increased fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:20670938 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0005533 increased body temperature IAGP N RGD:5509061 20141003 MGI PMID:21990309 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:20670938 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0005560 decreased circulating glucose level IAGP N RGD:5509061 20141003 MGI PMID:21990309 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20230330 MGI PMID:36398584 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0005659 decreased susceptibility to diet-induced obesity IAGP N RGD:5509061 20141003 MGI PMID:21990309 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0008898 abnormal acrosome morphology IAGP N RGD:5509061 20230330 MGI PMID:36398584 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0009234 absent sperm head IAGP N RGD:5509061 20230330 MGI PMID:36398584 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0009238 coiled sperm flagellum IAGP N RGD:5509061 20230330 MGI PMID:36398584 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20230330 MGI PMID:36398584 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0009643 abnormal urine homeostasis IAGP N RGD:5509061 20141003 MGI PMID:21990309 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:21990309 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0010028 aciduria IAGP N RGD:5509061 20141003 MGI PMID:20670938 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0010379 decreased respiratory quotient IAGP N RGD:5509061 20141003 MGI PMID:21990309 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0010953 abnormal fatty acid oxidation IAGP N RGD:5509061 20141003 MGI PMID:21990309 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0013288 premature acrosome reaction IAGP N RGD:5509061 20230330 MGI PMID:36398584 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20230330 MGI PMID:36398584 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0020451 decreased sperm progressive motility IAGP N RGD:5509061 20230330 MGI PMID:36398584 737567 Hadh hydroxyacyl-Coenzyme A dehydrogenase gene MP:0020550 multinucleated giant male germ cells IAGP N RGD:5509061 20230330 MGI PMID:36398584 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0000736 delayed muscle development IAGP N RGD:5509061 20141003 MGI PMID:17366633 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0000961 abnormal dorsal root ganglion morphology IAGP N RGD:5509061 20141003 MGI PMID:15733626 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0000965 abnormal sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:15733626 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0000969 abnormal nociceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:15733626 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0000972 abnormal mechanoreceptor morphology IAGP N RGD:5509061 20141003 MGI PMID:15733626 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:17486104 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0001363 increased anxiety-related response IAGP N RGD:5509061 20150226 MGI PMID:23118208 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0001973 increased thermal nociceptive threshold IAGP N RGD:5509061 20141003 MGI PMID:15733626 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0002557 abnormal social/conspecific interaction behavior IAGP N RGD:5509061 20150226 MGI PMID:23118208 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:18026113 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:17366633 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0004275 abnormal postnatal subventricular zone morphology IAGP N RGD:5509061 20141003 MGI PMID:16636291 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0004799 increased susceptibility to experimental autoimmune encephalomyelitis IAGP N RGD:5509061 20141003 MGI PMID:17589510 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0005236 abnormal olfactory nerve morphology IAGP N RGD:5509061 20141003 MGI PMID:8873770 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0006092 abnormal olfactory sensory neuron morphology IAGP N RGD:5509061 20141003 MGI PMID:8873770 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0008566 increased interferon-gamma secretion IAGP N RGD:5509061 20141003 MGI PMID:17589510 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0008687 increased interleukin-2 secretion IAGP N RGD:5509061 20141003 MGI PMID:17589510 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:17366633 737568 Lgals1 lectin, galactose binding, soluble 1 gene MP:0031328 delayed skeletal muscle regeneration IAGP N RGD:5509061 20220106 MGI PMID:17366633 737572 Chad chondroadherin gene MP:0000063 decreased bone mineral density IAGP N RGD:5509061 20141003 MGI PMID:23755099 737572 Chad chondroadherin gene MP:0000130 abnormal trabecular bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23755099 737572 Chad chondroadherin gene MP:0003662 abnormal long bone epiphyseal plate proliferative zone IAGP N RGD:5509061 20141003 MGI PMID:23755099 737572 Chad chondroadherin gene MP:0003797 abnormal compact bone morphology IAGP N RGD:5509061 20141003 MGI PMID:23755099 737572 Chad chondroadherin gene MP:0004991 decreased bone strength IAGP N RGD:5509061 20141003 MGI PMID:23755099 737572 Chad chondroadherin gene MP:0006398 increased long bone epiphyseal plate size IAGP N RGD:5509061 20141003 MGI PMID:23755099 737572 Chad chondroadherin gene MP:0009347 increased trabecular bone thickness IAGP N RGD:5509061 20141003 MGI PMID:23755099 737572 Chad chondroadherin gene MP:0010025 decreased total body fat amount IAGP N RGD:5509061 20141003 MGI PMID:23755099 737574 Opn5 opsin 5 gene MP:0005253 abnormal eye physiology IAGP N RGD:5509061 20171012 MGI PMID:26392540 737574 Opn5 opsin 5 gene MP:0020476 abnormal circardian behavior entrainment IAGP N RGD:5509061 20171012 MGI PMID:26392540 737575 Chrna5 cholinergic receptor, nicotinic, alpha polypeptide 5 gene MP:0000219 increased neutrophil cell number IEA N RGD:5509061 20211021 MGI 737575 Chrna5 cholinergic receptor, nicotinic, alpha polypeptide 5 gene MP:0002606 increased basophil cell number IEA N RGD:5509061 20240523 MGI 737575 Chrna5 cholinergic receptor, nicotinic, alpha polypeptide 5 gene MP:0002875 decreased erythrocyte cell number IEA N RGD:5509061 20201022 MGI 737575 Chrna5 cholinergic receptor, nicotinic, alpha polypeptide 5 gene MP:0002887 decreased susceptibility to pharmacologically induced seizures IAGP N RGD:5509061 20141003 MGI PMID:14996991 737575 Chrna5 cholinergic receptor, nicotinic, alpha polypeptide 5 gene MP:0005016 decreased lymphocyte cell number IEA N RGD:5509061 20211021 MGI 737575 Chrna5 cholinergic receptor, nicotinic, alpha polypeptide 5 gene MP:0011239 abnormal skin coloration IEA N RGD:5509061 20190502 MGI 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0000208 decreased hematocrit IAGP N RGD:5509061 20141003 MGI PMID:5427253 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0000240 extramedullary hematopoiesis IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0000274 enlarged heart IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0000689 abnormal spleen morphology IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0000691 enlarged spleen IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0001212 skin lesions IAGP N RGD:5509061 20141003 MGI PMID:5427253 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:5427253 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0001577 anemia IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0001923 reduced female fertility IAGP N RGD:5509061 20141003 MGI PMID:5427253 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:10791995 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002082 postnatal lethality IAGP N RGD:5509061 20141003 MGI PMID:5427253 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002447 abnormal erythrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002591 decreased mean corpuscular volume IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002593 high mean erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:5427253 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:5427253 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002640 reticulocytosis IAGP N RGD:5509061 20141003 MGI PMID:5507573 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002642 anisocytosis IAGP N RGD:5509061 20141003 MGI PMID:5507573 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002643 poikilocytosis IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002810 microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002813 microcytosis IAGP N RGD:5509061 20141003 MGI PMID:5427253 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:5427253 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002874 decreased hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:5507573 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0002875 decreased erythrocyte cell number IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0003717 pallor IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0003718 maternal effect IAGP N RGD:5509061 20141003 MGI PMID:5427253 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0004952 increased spleen weight IAGP N RGD:5509061 20141003 MGI PMID:5427253 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0005562 decreased mean corpuscular hemoglobin IAGP N RGD:5509061 20141003 MGI PMID:5427253 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0005637 abnormal iron homeostasis IAGP N RGD:5509061 20141003 MGI PMID:15994289 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0005642 decreased mean corpuscular hemoglobin concentration IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:5427253 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0008388 hypochromic microcytic anemia IAGP N RGD:5509061 20141003 MGI PMID:5507573 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0008476 increased spleen red pulp amount IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:10791995 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0008743 decreased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0008807 increased liver iron level IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0008808 decreased spleen iron level IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0008956 decreased cellular hemoglobin content IAGP N RGD:5509061 20141003 MGI PMID:5427253 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0010035 increased erythrocyte clearance IAGP N RGD:5509061 20141003 MGI PMID:5507573 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0010163 hemolysis IAGP N RGD:5509061 20141003 MGI PMID:5507573 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0010376 decreased kidney iron level IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:5427253 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0011188 increased erythrocyte protoporphyrin level IAGP N RGD:5509061 20141003 MGI PMID:658175 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0020366 decreased brain iron level IAGP N RGD:5509061 20161020 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0020368 decreased heart iron level IAGP N RGD:5509061 20161020 MGI PMID:15849611 737579 Slc11a2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 gene MP:0031084 decreased erythrocyte osmotic fragility IAGP N RGD:5509061 20200716 MGI PMID:5427253 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0000161 scoliosis IAGP N RGD:5509061 20141003 MGI PMID:12138199 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0000733 abnormal muscle development IAGP N RGD:5509061 20141003 MGI PMID:12138199 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0000747 muscle weakness IAGP N RGD:5509061 20141003 MGI PMID:12138199 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0000755 hindlimb paralysis IAGP N RGD:5509061 20141003 MGI PMID:21303860 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0000759 abnormal skeletal muscle morphology IAGP N RGD:5509061 20141003 MGI PMID:21303860 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12138199 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:21303860 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:22067542 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0001265 decreased body size IAGP N RGD:5509061 20141003 MGI PMID:12138199 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0001344 blepharoptosis IAGP N RGD:5509061 20141003 MGI PMID:22067542 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0001349 excessive tearing IAGP N RGD:5509061 20170907 MGI PMID:22067542 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22067542 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:22067542 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0001780 decreased brown adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12138199 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0001921 reduced fertility IAGP N RGD:5509061 20141003 MGI PMID:21303860 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:21303860 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:22067542 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:12138199 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0003084 abnormal skeletal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:12138199 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:21303860 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0004087 abnormal muscle fiber morphology IAGP N RGD:5509061 20141003 MGI PMID:22067542 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0004090 abnormal sarcomere morphology IAGP N RGD:5509061 20141003 MGI PMID:22067542 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0004091 abnormal Z line morphology IAGP N RGD:5509061 20141003 MGI PMID:21303860 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0004232 decreased muscle weight IAGP N RGD:5509061 20141003 MGI PMID:22067542 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0004233 abnormal muscle weight IAGP N RGD:5509061 20141003 MGI PMID:22067542 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0005439 decreased glycogen level IAGP N RGD:5509061 20141003 MGI PMID:12138199 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20141003 MGI PMID:12138199 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0009403 increased variability of skeletal muscle fiber size IAGP N RGD:5509061 20141003 MGI PMID:21303860 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0010052 increased grip strength IAGP N RGD:5509061 20170907 MGI PMID:22067542 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:22067542 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0010398 decreased liver glycogen level IAGP N RGD:5509061 20141003 MGI PMID:12138199 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0010399 decreased skeletal muscle glycogen level IAGP N RGD:5509061 20141003 MGI PMID:12138199 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12138199 737581 Acta1 actin alpha 1, skeletal muscle gene MP:0030140 facial muscle atrophy IAGP N RGD:5509061 20171005 MGI PMID:22067542 737587 Irs3 insulin receptor substrate 3 gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20141003 MGI PMID:12502742 737587 Irs3 insulin receptor substrate 3 gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:12502742 737587 Irs3 insulin receptor substrate 3 gene MP:0001783 decreased white adipose tissue amount IAGP N RGD:5509061 20141003 MGI PMID:12502742 737587 Irs3 insulin receptor substrate 3 gene MP:0002079 increased circulating insulin level IAGP N RGD:5509061 20141003 MGI PMID:12502742 737587 Irs3 insulin receptor substrate 3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:10364263 737587 Irs3 insulin receptor substrate 3 gene MP:0002644 decreased circulating triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12502742 737587 Irs3 insulin receptor substrate 3 gene MP:0002702 decreased circulating free fatty acids level IAGP N RGD:5509061 20141003 MGI PMID:12502742 737587 Irs3 insulin receptor substrate 3 gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20141003 MGI PMID:12502742 737587 Irs3 insulin receptor substrate 3 gene MP:0005318 decreased triglyceride level IAGP N RGD:5509061 20141003 MGI PMID:12502742 737587 Irs3 insulin receptor substrate 3 gene MP:0005331 insulin resistance IAGP N RGD:5509061 20141003 MGI PMID:12502742 737587 Irs3 insulin receptor substrate 3 gene MP:0005335 abnormal gonadal fat pad morphology IAGP N RGD:5509061 20141003 MGI PMID:12502742 737587 Irs3 insulin receptor substrate 3 gene MP:0005491 pancreatic islet hyperplasia IAGP N RGD:5509061 20141003 MGI PMID:12502742 737587 Irs3 insulin receptor substrate 3 gene MP:0005668 decreased circulating leptin level IAGP N RGD:5509061 20141003 MGI PMID:12502742 737587 Irs3 insulin receptor substrate 3 gene MP:0009113 increased pancreatic beta cell mass IAGP N RGD:5509061 20141003 MGI PMID:12502742 737590 Madd MAP-kinase activating death domain gene MP:0001053 abnormal neuromuscular synapse morphology IAGP N RGD:5509061 20141003 MGI PMID:11359932 737590 Madd MAP-kinase activating death domain gene MP:0001559 hyperglycemia IAGP N RGD:5509061 20160915 MGI PMID:24379354 737590 Madd MAP-kinase activating death domain gene MP:0001944 abnormal pancreas morphology IAGP N RGD:5509061 20160915 MGI PMID:24379354 737590 Madd MAP-kinase activating death domain gene MP:0001953 respiratory failure IAGP N RGD:5509061 20141003 MGI PMID:11359932 737590 Madd MAP-kinase activating death domain gene MP:0002578 impaired ability to fire action potentials IAGP N RGD:5509061 20141003 MGI PMID:11359932 737590 Madd MAP-kinase activating death domain gene MP:0002727 decreased circulating insulin level IAGP N RGD:5509061 20160915 MGI PMID:24379354 737590 Madd MAP-kinase activating death domain gene MP:0002910 abnormal excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12388783 737590 Madd MAP-kinase activating death domain gene MP:0003059 decreased insulin secretion IAGP N RGD:5509061 20160915 MGI PMID:24379354 737590 Madd MAP-kinase activating death domain gene MP:0003562 abnormal pancreatic beta cell physiology IAGP N RGD:5509061 20160915 MGI PMID:24379354 737590 Madd MAP-kinase activating death domain gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20141003 MGI PMID:12388783 737590 Madd MAP-kinase activating death domain gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:11359932 737590 Madd MAP-kinase activating death domain gene MP:0004769 abnormal synaptic vesicle morphology IAGP N RGD:5509061 20141003 MGI PMID:12388783 737590 Madd MAP-kinase activating death domain gene MP:0004792 abnormal synaptic vesicle number IAGP N RGD:5509061 20141003 MGI PMID:11359932 737590 Madd MAP-kinase activating death domain gene MP:0005215 abnormal pancreatic islet morphology IAGP N RGD:5509061 20160915 MGI PMID:24379354 737590 Madd MAP-kinase activating death domain gene MP:0005217 abnormal pancreatic beta cell morphology IAGP N RGD:5509061 20160915 MGI PMID:24379354 737590 Madd MAP-kinase activating death domain gene MP:0005293 impaired glucose tolerance IAGP N RGD:5509061 20160915 MGI PMID:24379354 737590 Madd MAP-kinase activating death domain gene MP:0005498 hyporesponsive to tactile stimuli IAGP N RGD:5509061 20141003 MGI PMID:11359932 737590 Madd MAP-kinase activating death domain gene MP:0010819 primary atelectasis IAGP N RGD:5509061 20141003 MGI PMID:11359932 737590 Madd MAP-kinase activating death domain gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20141003 MGI PMID:11359932 737590 Madd MAP-kinase activating death domain gene MP:0011268 biphasic excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240418 MGI PMID:12388783 737590 Madd MAP-kinase activating death domain gene MP:0013279 increased fasting circulating glucose level IAGP N RGD:5509061 20160915 MGI PMID:24379354 737592 Selenop selenoprotein P gene MP:0000592 short tail IAGP N RGD:5509061 20141003 MGI PMID:12521380 737592 Selenop selenoprotein P gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:17311913 737592 Selenop selenoprotein P gene MP:0001258 decreased body length IAGP N RGD:5509061 20141003 MGI PMID:12521380 737592 Selenop selenoprotein P gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:12521380 737592 Selenop selenoprotein P gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:23038251 737592 Selenop selenoprotein P gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:12521380 737592 Selenop selenoprotein P gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:17311913 737592 Selenop selenoprotein P gene MP:0001402 decreased locomotor activity IAGP N RGD:5509061 20141003 MGI PMID:22487427 737592 Selenop selenoprotein P gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12521380 737592 Selenop selenoprotein P gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:12574155 737592 Selenop selenoprotein P gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:22487427 737592 Selenop selenoprotein P gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:12521380 737592 Selenop selenoprotein P gene MP:0001406 abnormal gait IAGP N RGD:5509061 20141003 MGI PMID:23038251 737592 Selenop selenoprotein P gene MP:0001407 short stride length IAGP N RGD:5509061 20141003 MGI PMID:17311913 737592 Selenop selenoprotein P gene MP:0001442 decreased grooming behavior IAGP N RGD:5509061 20141003 MGI PMID:22487427 737592 Selenop selenoprotein P gene MP:0001463 abnormal spatial learning IAGP N RGD:5509061 20141003 MGI PMID:22487427 737592 Selenop selenoprotein P gene MP:0001513 limb grasping IAGP N RGD:5509061 20141003 MGI PMID:23038251 737592 Selenop selenoprotein P gene MP:0001523 impaired righting response IAGP N RGD:5509061 20141003 MGI PMID:17311913 737592 Selenop selenoprotein P gene MP:0001775 abnormal selenium level IAGP N RGD:5509061 20141003 MGI PMID:12574155 737592 Selenop selenoprotein P gene MP:0001775 abnormal selenium level IAGP N RGD:5509061 20141003 MGI PMID:17311913 737592 Selenop selenoprotein P gene MP:0001775 abnormal selenium level IAGP N RGD:5509061 20141003 MGI PMID:20015939 737592 Selenop selenoprotein P gene MP:0001775 abnormal selenium level IAGP N RGD:5509061 20141003 MGI PMID:23038251 737592 Selenop selenoprotein P gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:12574155 737592 Selenop selenoprotein P gene MP:0001922 reduced male fertility IAGP N RGD:5509061 20141003 MGI PMID:17311913 737592 Selenop selenoprotein P gene MP:0001935 decreased litter size IAGP N RGD:5509061 20141003 MGI PMID:17311913 737592 Selenop selenoprotein P gene MP:0002066 abnormal motor capabilities/coordination/movement IAGP N RGD:5509061 20141003 MGI PMID:22487427 737592 Selenop selenoprotein P gene MP:0002068 abnormal parental behavior IAGP N RGD:5509061 20141003 MGI PMID:12574155 737592 Selenop selenoprotein P gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12521380 737592 Selenop selenoprotein P gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:12574155 737592 Selenop selenoprotein P gene MP:0002687 oligozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23038251 737592 Selenop selenoprotein P gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:22487427 737592 Selenop selenoprotein P gene MP:0003325 decreased liver function IAGP N RGD:5509061 20141003 MGI PMID:18424738 737592 Selenop selenoprotein P gene MP:0003887 increased hepatocyte apoptosis IAGP N RGD:5509061 20141003 MGI PMID:18424738 737592 Selenop selenoprotein P gene MP:0005027 increased susceptibility to parasitic infection IAGP N RGD:5509061 20141003 MGI PMID:18424738 737592 Selenop selenoprotein P gene MP:0005578 teratozoospermia IAGP N RGD:5509061 20141003 MGI PMID:23038251 737592 Selenop selenoprotein P gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20141003 MGI PMID:17311913 737592 Selenop selenoprotein P gene MP:0008892 abnormal sperm flagellum morphology IAGP N RGD:5509061 20141003 MGI PMID:17311913 737592 Selenop selenoprotein P gene MP:0009243 hairpin sperm flagellum IAGP N RGD:5509061 20141003 MGI PMID:17311913 737592 Selenop selenoprotein P gene MP:0009763 increased susceptibility to induced morbidity/mortality IAGP N RGD:5509061 20141003 MGI PMID:17311913 737592 Selenop selenoprotein P gene MP:0009831 abnormal sperm midpiece morphology IAGP N RGD:5509061 20141003 MGI PMID:17311913 737592 Selenop selenoprotein P gene MP:0010053 decreased grip strength IAGP N RGD:5509061 20141003 MGI PMID:22487427 737592 Selenop selenoprotein P gene MP:0010180 increased susceptibility to weight loss IAGP N RGD:5509061 20141003 MGI PMID:12574155 737592 Selenop selenoprotein P gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12574155 737592 Selenop selenoprotein P gene MP:0011770 increased urine selenium level IAGP N RGD:5509061 20141003 MGI PMID:23038251 737592 Selenop selenoprotein P gene MP:0014464 decreased sperm mitochondrial sheath size IAGP N RGD:5509061 20240613 MGI PMID:17311913 737595 Esm1 endothelial cell-specific molecule 1 gene MP:0002792 abnormal retina vasculature morphology IAGP N RGD:5509061 20240307 MGI PMID:25057127 737595 Esm1 endothelial cell-specific molecule 1 gene MP:0003071 decreased vascular permeability IAGP N RGD:5509061 20240307 MGI PMID:25057127 737595 Esm1 endothelial cell-specific molecule 1 gene MP:0004003 abnormal vascular endothelial cell physiology IAGP N RGD:5509061 20240307 MGI PMID:25057127 737595 Esm1 endothelial cell-specific molecule 1 gene MP:0005602 decreased angiogenesis IAGP N RGD:5509061 20240307 MGI PMID:25057127 737595 Esm1 endothelial cell-specific molecule 1 gene MP:0006055 abnormal vascular endothelial cell morphology IAGP N RGD:5509061 20240307 MGI PMID:25057127 737595 Esm1 endothelial cell-specific molecule 1 gene MP:0006059 decreased susceptibility to ischemic brain injury IAGP N RGD:5509061 20240307 MGI PMID:25057127 737595 Esm1 endothelial cell-specific molecule 1 gene MP:0009858 abnormal cellular extravasation IAGP N RGD:5509061 20240307 MGI PMID:25057127 737595 Esm1 endothelial cell-specific molecule 1 gene MP:0010144 abnormal tumor vascularization IAGP N RGD:5509061 20240307 MGI PMID:25057127 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0000131 abnormal long bone epiphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0000133 abnormal long bone metaphysis morphology IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0000162 lordosis IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0000164 abnormal cartilage development IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0000165 abnormal long bone hypertrophic chondrocyte zone IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0000445 short snout IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0001523 impaired righting response IEA N RGD:5509061 20170105 MGI 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0002115 abnormal limb bone morphology IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0002427 disproportionate dwarf IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0004340 short scapula IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0004592 small mandible IAGP N RGD:5509061 20171214 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0004686 decreased length of long bones IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0010029 abnormal basicranium morphology IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:12732630 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0011100 preweaning lethality, complete penetrance IEA N RGD:5509061 20201231 MGI 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0011175 platyspondylia IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0012175 flat face IAGP N RGD:5509061 20141003 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0030124 middle ear ossicle hypoplasia IAGP N RGD:5509061 20171005 MGI PMID:9988279 737597 Hapln1 hyaluronan and proteoglycan link protein 1 gene MP:0030420 short basicranium IAGP N RGD:5509061 20171214 MGI PMID:9988279 737600 Uts2 urotensin 2 gene MP:0000183 decreased circulating LDL cholesterol level IAGP N RGD:5509061 20141106 MGI PMID:21376094 737600 Uts2 urotensin 2 gene MP:0001556 increased circulating HDL cholesterol level IAGP N RGD:5509061 20141106 MGI PMID:21376094 737600 Uts2 urotensin 2 gene MP:0005278 abnormal cholesterol homeostasis IAGP N RGD:5509061 20141106 MGI PMID:21376094 737600 Uts2 urotensin 2 gene MP:0005584 abnormal enzyme/coenzyme activity IAGP N RGD:5509061 20141106 MGI PMID:21376094 737600 Uts2 urotensin 2 gene MP:0010331 abnormal apolipoprotein level IAGP N RGD:5509061 20141106 MGI PMID:21376094 737600 Uts2 urotensin 2 gene MP:0031268 decreased susceptibility to diet-induced hepatic steatosis IAGP N RGD:5509061 20210610 MGI PMID:21376094 737602 Stag3 STAG3 cohesin complex component gene MP:0000063 decreased bone mineral density IEA N RGD:5509061 20210128 MGI 737602 Stag3 STAG3 cohesin complex component gene MP:0001147 small testis IEA N RGD:5509061 20210128 MGI 737602 Stag3 STAG3 cohesin complex component gene MP:0001925 male infertility IEA N RGD:5509061 20210826 MGI 737602 Stag3 STAG3 cohesin complex component gene MP:0001926 female infertility IEA N RGD:5509061 20210826 MGI 737602 Stag3 STAG3 cohesin complex component gene MP:0003795 abnormal bone structure IEA N RGD:5509061 20160421 MGI 737602 Stag3 STAG3 cohesin complex component gene MP:0003961 decreased lean body mass IEA N RGD:5509061 20210128 MGI 737602 Stag3 STAG3 cohesin complex component gene MP:0004805 absent oocytes IEA N RGD:5509061 20111116 MGI 737602 Stag3 STAG3 cohesin complex component gene MP:0005159 azoospermia IEA N RGD:5509061 20111116 MGI 737602 Stag3 STAG3 cohesin complex component gene MP:0005169 abnormal male meiosis IAGP N RGD:5509061 20210304 MGI PMID:30853435 737602 Stag3 STAG3 cohesin complex component gene MP:0005568 increased circulating total protein level IEA N RGD:5509061 20240523 MGI 737602 Stag3 STAG3 cohesin complex component gene MP:0009451 abnormal chromosomal synapsis IAGP N RGD:5509061 20210304 MGI PMID:30853435 737602 Stag3 STAG3 cohesin complex component gene MP:0009452 abnormal synaptonemal complex IAGP N RGD:5509061 20210304 MGI PMID:30853435 737602 Stag3 STAG3 cohesin complex component gene MP:0010024 increased total body fat amount IEA N RGD:5509061 20210128 MGI 737602 Stag3 STAG3 cohesin complex component gene MP:0010053 decreased grip strength IEA N RGD:5509061 20210128 MGI 737602 Stag3 STAG3 cohesin complex component gene MP:0010124 decreased bone mineral content IEA N RGD:5509061 20210128 MGI 737602 Stag3 STAG3 cohesin complex component gene MP:0010948 abnormal double-strand DNA break repair IAGP N RGD:5509061 20210304 MGI PMID:30853435 737602 Stag3 STAG3 cohesin complex component gene MP:0013279 increased fasting circulating glucose level IEA N RGD:5509061 20240523 MGI 737602 Stag3 STAG3 cohesin complex component gene MP:0014052 increased male germ cell apoptosis IAGP N RGD:5509061 20210304 MGI PMID:30853435 737604 Cldn11 claudin 11 gene MP:0000048 abnormal stria vascularis morphology IAGP N RGD:5509061 20141003 MGI PMID:15456848 737604 Cldn11 claudin 11 gene MP:0000745 tremors IAGP N RGD:5509061 20141003 MGI PMID:10612400 737604 Cldn11 claudin 11 gene MP:0001147 small testis IAGP N RGD:5509061 20141003 MGI PMID:10612400 737604 Cldn11 claudin 11 gene MP:0001156 abnormal spermatogenesis IAGP N RGD:5509061 20141003 MGI PMID:10612400 737604 Cldn11 claudin 11 gene MP:0001399 hyperactivity IEA N RGD:5509061 20210826 MGI 737604 Cldn11 claudin 11 gene MP:0001405 impaired coordination IAGP N RGD:5509061 20141003 MGI PMID:10612400 737604 Cldn11 claudin 11 gene MP:0001406 abnormal gait IEA N RGD:5509061 20210826 MGI 737604 Cldn11 claudin 11 gene MP:0001488 increased startle reflex IEA N RGD:5509061 20210826 MGI 737604 Cldn11 claudin 11 gene MP:0001515 abnormal grip strength IAGP N RGD:5509061 20141003 MGI PMID:10612400 737604 Cldn11 claudin 11 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:10612400 737604 Cldn11 claudin 11 gene MP:0001925 male infertility IAGP N RGD:5509061 20141003 MGI PMID:15456848 737604 Cldn11 claudin 11 gene MP:0001967 deafness IAGP N RGD:5509061 20141003 MGI PMID:15306639 737604 Cldn11 claudin 11 gene MP:0002216 abnormal seminiferous tubule morphology IAGP N RGD:5509061 20141003 MGI PMID:10612400 737604 Cldn11 claudin 11 gene MP:0003871 abnormal myelin sheath morphology IAGP N RGD:5509061 20141003 MGI PMID:10612400 737604 Cldn11 claudin 11 gene MP:0004404 cochlear outer hair cell degeneration IAGP N RGD:5509061 20141003 MGI PMID:15306639 737604 Cldn11 claudin 11 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:15306639 737604 Cldn11 claudin 11 gene MP:0004411 decreased endocochlear potential IAGP N RGD:5509061 20141003 MGI PMID:15456848 737604 Cldn11 claudin 11 gene MP:0004464 absent strial basal cell tight junctions IAGP N RGD:5509061 20141003 MGI PMID:15306639 737604 Cldn11 claudin 11 gene MP:0004464 absent strial basal cell tight junctions IAGP N RGD:5509061 20141003 MGI PMID:15456848 737604 Cldn11 claudin 11 gene MP:0004736 abnormal distortion product otoacoustic emission IAGP N RGD:5509061 20141003 MGI PMID:15306639 737604 Cldn11 claudin 11 gene MP:0005159 azoospermia IAGP N RGD:5509061 20141003 MGI PMID:10612400 737604 Cldn11 claudin 11 gene MP:0005565 increased blood urea nitrogen level IEA N RGD:5509061 20211021 MGI 737604 Cldn11 claudin 11 gene MP:0010748 abnormal visual evoked potential IAGP N RGD:5509061 20141003 MGI PMID:10612400 737604 Cldn11 claudin 11 gene MP:0011966 abnormal auditory brainstem response waveform shape IAGP N RGD:5509061 20141003 MGI PMID:15306639 737604 Cldn11 claudin 11 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15306639 737604 Cldn11 claudin 11 gene MP:0011967 increased or absent threshold for auditory brainstem response IAGP N RGD:5509061 20141003 MGI PMID:15456848 737604 Cldn11 claudin 11 gene MP:0020355 abnormal Sertoli cell barrier morphology IAGP N RGD:5509061 20160915 MGI PMID:10612400 737605 Hpgds hematopoietic prostaglandin D synthase gene MP:0000266 abnormal heart morphology IEA N RGD:5509061 20181227 MGI 737605 Hpgds hematopoietic prostaglandin D synthase gene MP:0000274 enlarged heart IEA N RGD:5509061 20181227 MGI 737605 Hpgds hematopoietic prostaglandin D synthase gene MP:0001246 mixed cellular infiltration to dermis IAGP N RGD:5509061 20141003 MGI PMID:16547141 737605 Hpgds hematopoietic prostaglandin D synthase gene MP:0001393 ataxia IAGP N RGD:5509061 20141003 MGI PMID:16624958 737605 Hpgds hematopoietic prostaglandin D synthase gene MP:0001785 edema IAGP N RGD:5509061 20141003 MGI PMID:23624557 737605 Hpgds hematopoietic prostaglandin D synthase gene MP:0001846 increased inflammatory response IAGP N RGD:5509061 20141003 MGI PMID:16547141 737605 Hpgds hematopoietic prostaglandin D synthase gene MP:0002083 premature death IAGP N RGD:5509061 20141003 MGI PMID:16624958 737605 Hpgds hematopoietic prostaglandin D synthase gene MP:0002182 abnormal astrocyte morphology IAGP N RGD:5509061 20141003 MGI PMID:16624958 737605 Hpgds hematopoietic prostaglandin D synthase gene MP:0002339 abnormal lymph node morphology IAGP N RGD:5509061 20141003 MGI PMID:16547141 737605 Hpgds hematopoietic prostaglandin D synthase gene MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20141003 MGI PMID:17283118 737605 Hpgds hematopoietic prostaglandin D synthase gene MP:0003009 abnormal cytokine secretion IAGP N RGD:5509061 20141003 MGI PMID:16547141 737605 Hpgds hematopoietic prostaglandin D synthase gene MP:0005088 increased acute inflammation IAGP N RGD:5509061 20141003 MGI PMID:16547141 737605 Hpgds hematopoietic prostaglandin D synthase gene MP:0005596 increased susceptibility to type I hypersensitivity reaction IAGP N RGD:5509061 20141003 MGI PMID:23624557 737605 Hpgds hematopoietic prostaglandin D synthase gene MP:0006043 decreased apoptosis IAGP N RGD:5509061 20141003 MGI PMID:16624958 737608 Ckmt2 creatine kinase, mitochondrial 2 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:11713654 737608 Ckmt2 creatine kinase, mitochondrial 2 gene MP:0001544 abnormal cardiovascular system physiology IAGP N RGD:5509061 20141003 MGI PMID:15639481 737608 Ckmt2 creatine kinase, mitochondrial 2 gene MP:0002106 abnormal muscle physiology IAGP N RGD:5509061 20141003 MGI PMID:11713654 737608 Ckmt2 creatine kinase, mitochondrial 2 gene MP:0002127 abnormal cardiovascular system morphology IAGP N RGD:5509061 20141003 MGI PMID:15639481 737608 Ckmt2 creatine kinase, mitochondrial 2 gene MP:0002625 heart left ventricle hypertrophy IAGP N RGD:5509061 20141003 MGI PMID:15639481 737608 Ckmt2 creatine kinase, mitochondrial 2 gene MP:0002753 dilated heart left ventricle IAGP N RGD:5509061 20141003 MGI PMID:15639481 737608 Ckmt2 creatine kinase, mitochondrial 2 gene MP:0002841 impaired skeletal muscle contractility IAGP N RGD:5509061 20141003 MGI PMID:11713654 737608 Ckmt2 creatine kinase, mitochondrial 2 gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20141003 MGI PMID:11713654 737608 Ckmt2 creatine kinase, mitochondrial 2 gene MP:0006264 decreased systemic arterial systolic blood pressure IAGP N RGD:5509061 20141003 MGI PMID:15639481 737608 Ckmt2 creatine kinase, mitochondrial 2 gene MP:0011951 increased cardiac stroke volume IAGP N RGD:5509061 20141003 MGI PMID:15639481 737610 Ap1b1 adaptor protein complex AP-1, beta 1 subunit gene MP:0000690 absent spleen IEA N RGD:5509061 20150806 MGI 737610 Ap1b1 adaptor protein complex AP-1, beta 1 subunit gene MP:0000694 spleen hypoplasia IEA N RGD:5509061 20150806 MGI 737610 Ap1b1 adaptor protein complex AP-1, beta 1 subunit gene MP:0003178 left pulmonary isomerism IEA N RGD:5509061 20150806 MGI 737610 Ap1b1 adaptor protein complex AP-1, beta 1 subunit gene MP:0004133 heterotaxia IEA N RGD:5509061 20150806 MGI 737610 Ap1b1 adaptor protein complex AP-1, beta 1 subunit gene MP:0004624 abnormal thoracic cage morphology IEA N RGD:5509061 20150806 MGI 737610 Ap1b1 adaptor protein complex AP-1, beta 1 subunit gene MP:0006063 abnormal inferior vena cava morphology IEA N RGD:5509061 20150806 MGI 737610 Ap1b1 adaptor protein complex AP-1, beta 1 subunit gene MP:0011055 abnormal respiratory motile cilium physiology IEA N RGD:5509061 20150806 MGI 737610 Ap1b1 adaptor protein complex AP-1, beta 1 subunit gene MP:0011252 situs inversus totalis IEA N RGD:5509061 20150806 MGI 737610 Ap1b1 adaptor protein complex AP-1, beta 1 subunit gene MP:0011649 immotile respiratory cilia IEA N RGD:5509061 20150806 MGI 737618 Pcsk1n proprotein convertase subtilisin/kexin type 1 inhibitor gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:20367757 737618 Pcsk1n proprotein convertase subtilisin/kexin type 1 inhibitor gene MP:0001364 decreased anxiety-related response IAGP N RGD:5509061 20141003 MGI PMID:20367757 737618 Pcsk1n proprotein convertase subtilisin/kexin type 1 inhibitor gene MP:0002757 decreased vertical activity IAGP N RGD:5509061 20141003 MGI PMID:20367757 737618 Pcsk1n proprotein convertase subtilisin/kexin type 1 inhibitor gene MP:0003313 abnormal locomotor activation IAGP N RGD:5509061 20141003 MGI PMID:20367757 737618 Pcsk1n proprotein convertase subtilisin/kexin type 1 inhibitor gene MP:0003908 decreased stereotypic behavior IAGP N RGD:5509061 20141003 MGI PMID:20367757 7394747 asp3_m audiogenic seizure prone 3 (mouse) qtl MP:0001496 audiogenic seizures IAGP N RGD:5509061 20131107 MGI PMID:2052619 7394747 asp3_m audiogenic seizure prone 3 (mouse) qtl MP:0002083 premature death IAGP N RGD:5509061 20131107 MGI PMID:2052619 7394747 asp3_m audiogenic seizure prone 3 (mouse) qtl MP:0003631 nervous system phenotype IEA N RGD:704405 20131101 MGI Created by mouse qtl pipeline PMID:2052619 7394747 asp3_m audiogenic seizure prone 3 (mouse) qtl MP:0005386 behavior/neurological phenotype IEA N RGD:704405 20131101 MGI Created by mouse qtl pipeline PMID:2052619 7394747 asp3_m audiogenic seizure prone 3 (mouse) qtl MP:0010768 mortality/aging IEA N RGD:704405 20131101 MGI Created by mouse qtl pipeline PMID:2052619 7394747 asp3_m audiogenic seizure prone 3 (mouse) qtl MP:0031391 increased locomotor activity IAGP N RGD:5509061 20220421 MGI PMID:2052619 7394748 Mom5_m modifier of Min 5 (mouse) qtl MP:0002006 neoplasm IEA N RGD:704405 20131101 MGI Created by mouse qtl pipeline PMID:19574546 7394748 Mom5_m modifier of Min 5 (mouse) qtl MP:0002053 decreased incidence of induced tumors IAGP N RGD:5509061 20131108 MGI PMID:19574546 7394748 Mom5_m modifier of Min 5 (mouse) qtl MP:0002404 increased intestinal adenoma incidence IAGP N RGD:5509061 20131108 MGI PMID:19574546 7394748 Mom5_m modifier of Min 5 (mouse) qtl MP:0005381 digestive/alimentary phenotype IEA N RGD:704405 20231117 MGI Created by mouse qtl pipeline PMID:19574546 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0000812 abnormal dentate gyrus morphology IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0000849 abnormal cerebellum morphology IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0000950 abnormal seizure response to pharmacological agent IAGP N RGD:5509061 20210401 MGI PMID:32853550 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0001325 abnormal retina morphology IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0001326 retina degeneration IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0001393 ataxia IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0001650 abnormal seizure response to electrical stimulation IAGP N RGD:5509061 20210401 MGI PMID:32853550 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0002066 abnormal motor capabilities/coordination/movement IEA N RGD:5509061 20141003 MGI 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0002083 premature death IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0002206 abnormal CNS synaptic transmission IAGP N RGD:5509061 20210401 MGI PMID:32853550 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0002229 neurodegeneration IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0003203 increased neuron apoptosis IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0003635 abnormal synaptic transmission IAGP N RGD:5509061 20210401 MGI PMID:32853550 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0004753 abnormal miniature excitatory postsynaptic currents IAGP N RGD:5509061 20210401 MGI PMID:32853550 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0004807 abnormal paired-pulse inhibition IAGP N RGD:5509061 20210401 MGI PMID:32853550 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0005386 behavior/neurological phenotype IAGP N RGD:5509061 20210401 MGI PMID:32853550 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0005402 abnormal action potential IAGP N RGD:5509061 20210401 MGI PMID:32853550 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0006068 abnormal retina horizontal cell morphology IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0008067 retina ganglion cell degeneration IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0008103 amacrine cell degeneration IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0008265 abnormal hippocampus CA2 region morphology IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0008450 retina photoreceptor degeneration IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0008840 abnormal spike wave discharge IAGP N RGD:5509061 20210401 MGI PMID:32853550 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0008924 decreased cerebellar granule cell number IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0009435 abnormal miniature inhibitory postsynaptic currents IAGP N RGD:5509061 20210401 MGI PMID:32853550 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0009956 abnormal cerebellar layer morphology IAGP N RGD:5509061 20190815 MGI PMID:25061210 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0014382 increased miniature inhibitory postsynaptic current frequency IAGP N RGD:5509061 20240404 MGI PMID:32853550 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0014384 increased miniature inhibitory postsynaptic current amplitude IAGP N RGD:5509061 20240404 MGI PMID:32853550 7488861 n-TRtct5 nuclear encoded tRNA arginine 5 (anticodon TCT) gene MP:0021081 abnormal ribosomal stalling IAGP N RGD:5509061 20220310 MGI PMID:25061210 7987884 Arhgap23 Rho GTPase activating protein 23 gene MP:0000198 decreased circulating phosphate level IEA N RGD:5509061 20211021 MGI 7987884 Arhgap23 Rho GTPase activating protein 23 gene MP:0005419 decreased circulating serum albumin level IEA N RGD:5509061 20210520 MGI 8181299 Haglr Hoxd antisense growth associated long non-coding RNA gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24381249 8181299 Haglr Hoxd antisense growth associated long non-coding RNA gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20141003 MGI PMID:24381249 8181299 Haglr Hoxd antisense growth associated long non-coding RNA gene MP:0011086 postnatal lethality, incomplete penetrance IAGP N RGD:5509061 20141003 MGI PMID:24381249 8181320 Halr1 Hoxa adjacent long noncoding RNA 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24381249 8181320 Halr1 Hoxa adjacent long noncoding RNA 1 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230126 MGI PMID:29420831 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0000159 abnormal xiphoid process morphology IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0000414 alopecia IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0000748 progressive muscle weakness IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0000757 herniated abdominal wall IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0001262 decreased body weight IAGP N RGD:5509061 20141003 MGI PMID:24381249 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0001262 decreased body weight IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0001513 limb grasping IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0001732 postnatal growth retardation IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0003704 abnormal hair follicle development IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0003786 premature aging IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0003961 decreased lean body mass IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0004819 decreased skeletal muscle mass IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0008770 decreased survivor rate IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0008844 decreased subcutaneous adipose tissue amount IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0009422 decreased gastrocnemius weight IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0009428 decreased tibialis anterior weight IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0009932 skin fibrosis IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0014143 decreased body fat mass IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20161229 MGI PMID:25909911 8181341 Lncpint long non-protein coding RNA, Trp53 induced transcript gene MP:0031253 lordokyphosis IAGP N RGD:5509061 20210610 MGI PMID:25909911 8548915 Xndc1 Xrcc1 N-terminal domain containing 1 gene MP:0004613 fusion of vertebral arches IEA N RGD:5509061 20201231 MGI 8552704 Cia43_m collagen induced arthritis QTL 43 (mouse) qtl MP:0003724 increased susceptibility to induced arthritis IAGP N RGD:5509061 20140502 MGI PMID:19234197 8552704 Cia43_m collagen induced arthritis QTL 43 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20140425 MGI Created by mouse qtl pipeline PMID:19234197 8552704 Cia43_m collagen induced arthritis QTL 43 (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20140425 MGI Created by mouse qtl pipeline PMID:19234197 8552707 Cia23_m collagen induced arthritis QTL 23 (mouse) qtl MP:0001845 abnormal inflammatory response IAGP N RGD:5509061 20140501 MGI PMID:11433381 8552707 Cia23_m collagen induced arthritis QTL 23 (mouse) qtl MP:0001876 decreased inflammatory response IAGP N RGD:5509061 20140502 MGI PMID:11433381 8552707 Cia23_m collagen induced arthritis QTL 23 (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20140425 MGI Created by mouse qtl pipeline PMID:11433381 8655599 Cia5c_m collagen induced arthritis QTL 5c (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20140516 MGI Created by mouse qtl pipeline PMID:15716976 8655599 Cia5c_m collagen induced arthritis QTL 5c (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20140516 MGI Created by mouse qtl pipeline PMID:15716976 8655600 Cia5b_m collagen induced arthritis QTL 5b (mouse) qtl MP:0005387 immune system phenotype IEA N RGD:704405 20140516 MGI Created by mouse qtl pipeline PMID:15716976 8655600 Cia5b_m collagen induced arthritis QTL 5b (mouse) qtl MP:0005390 skeleton phenotype IEA N RGD:704405 20140516 MGI Created by mouse qtl pipeline PMID:15716976 8655679 Ptgs2os2 prostaglandin-endoperoxide synthase 2, opposite strand 2 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24381249 8661275 Mannr Mecom adjacent non-protein coding RNA gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141003 MGI PMID:24381249 8693267 Rubie RNA upstream of Bmp4 expressed in inner ear gene MP:0000037 abnormal lateral semicircular canal morphology IAGP N RGD:5509061 20141003 MGI PMID:22253730 8693267 Rubie RNA upstream of Bmp4 expressed in inner ear gene MP:0001394 circling IAGP N RGD:5509061 20200402 MGI PMID:31784461 8693267 Rubie RNA upstream of Bmp4 expressed in inner ear gene MP:0001395 bidirectional circling IAGP N RGD:5509061 20141003 MGI PMID:22253730 8693267 Rubie RNA upstream of Bmp4 expressed in inner ear gene MP:0001399 hyperactivity IAGP N RGD:5509061 20141003 MGI PMID:22253730 8693267 Rubie RNA upstream of Bmp4 expressed in inner ear gene MP:0011238 abnormal inner ear development IAGP N RGD:5509061 20141003 MGI PMID:22253730 9586081 Foxi3 forkhead box I3 gene MP:0000018 small ears IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0000049 abnormal middle ear morphology IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0000074 abnormal neurocranium morphology IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0000111 cleft palate IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0000438 abnormal cranium morphology IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0000453 absent mouth IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0000455 abnormal maxilla morphology IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0000458 abnormal mandible morphology IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0000705 athymia IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0000919 cranioschisis IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0001082 abnormal geniculate ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:26550799 9586081 Foxi3 forkhead box I3 gene MP:0001092 abnormal trigeminal ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:26550799 9586081 Foxi3 forkhead box I3 gene MP:0001262 decreased body weight IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0001284 absent vibrissae IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0001943 abnormal respiration IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0003138 absent tympanic ring IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0003703 abnormal vestibulocochlear ganglion morphology IAGP N RGD:5509061 20200310 MGI PMID:26550799 9586081 Foxi3 forkhead box I3 gene MP:0003743 abnormal facial morphology IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0003861 abnormal nervous system development IAGP N RGD:5509061 20200310 MGI PMID:26550799 9586081 Foxi3 forkhead box I3 gene MP:0003874 absent pharyngeal arches IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0004204 absent stapes IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0004318 absent incus IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0004318 absent incus IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0004319 absent malleus IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0004319 absent malleus IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0004423 abnormal temporal bone squamous part morphology IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0004455 pterygoid bone hypoplasia IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0004467 absent zygomatic bone IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0005107 abnormal stapes morphology IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0005249 abnormal palatine bone morphology IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0005270 abnormal zygomatic bone morphology IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0005272 abnormal temporal bone morphology IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0005579 absent outer ear IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0005587 abnormal Meckel's cartilage morphology IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0006031 abnormal pharyngeal pouch morphology IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0006285 absent inner ear IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0008863 craniofacial asymmetry IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0009674 decreased birth weight IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0009703 decreased birth body size IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0009880 decreased mouth size IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0011085 postnatal lethality, complete penetrance IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0011087 neonatal lethality, complete penetrance IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0011108 embryonic lethality during organogenesis, incomplete penetrance IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0011173 abnormal otic placode morphology IAGP N RGD:5509061 20200310 MGI PMID:26550799 9586081 Foxi3 forkhead box I3 gene MP:0012761 increased cranial neural crest cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0013504 increased embryonic tissue cell apoptosis IAGP N RGD:5509061 20200310 MGI PMID:26550799 9586081 Foxi3 forkhead box I3 gene MP:0030064 small face IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0030085 syngnathia IAGP N RGD:5509061 20200310 MGI PMID:24650709 9586081 Foxi3 forkhead box I3 gene MP:0030085 syngnathia IAGP N RGD:5509061 20230713 MGI PMID:37041148 9586081 Foxi3 forkhead box I3 gene MP:0030119 abnormal retrotympanic process morphology IAGP N RGD:5509061 20230713 MGI PMID:37041148 9587780 Afw16_m abdominal fat weight QTL 16 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141023 MGI PMID:18008102 9587780 Afw16_m abdominal fat weight QTL 16 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20141017 MGI Created by mouse qtl pipeline PMID:18008102 9587781 Afw17_m abdominal fat weight QTL 17 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141023 MGI PMID:11116089 9587781 Afw17_m abdominal fat weight QTL 17 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20141017 MGI Created by mouse qtl pipeline PMID:11116089 9587782 Afw14_m abdominal fat weight QTL 14 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141023 MGI PMID:11116089 9587782 Afw14_m abdominal fat weight QTL 14 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20141017 MGI Created by mouse qtl pipeline PMID:11116089 9587783 Afw15_m abdominal fat weight QTL 15 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141023 MGI PMID:11116089 9587783 Afw15_m abdominal fat weight QTL 15 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20141017 MGI Created by mouse qtl pipeline PMID:11116089 9587784 Afw13_m abdominal fat weight QTL 13 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141023 MGI PMID:18008102 9587784 Afw13_m abdominal fat weight QTL 13 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20141017 MGI Created by mouse qtl pipeline PMID:18008102 9587785 Afw19_m abdominal fat weight QTL 19 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141023 MGI PMID:11116089 9587785 Afw19_m abdominal fat weight QTL 19 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20141017 MGI Created by mouse qtl pipeline PMID:11116089 9587786 Afw18_m abdominal fat weight QTL 18 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141023 MGI PMID:11116089 9587786 Afw18_m abdominal fat weight QTL 18 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20141017 MGI Created by mouse qtl pipeline PMID:11116089 9587787 Afw12_m abdominal fat weight QTL 12 (mouse) qtl MP:0000010 abnormal abdominal fat pad morphology IAGP N RGD:5509061 20141023 MGI PMID:11116089 9587787 Afw12_m abdominal fat weight QTL 12 (mouse) qtl MP:0005375 adipose tissue phenotype IEA N RGD:704405 20141017 MGI Created by mouse qtl pipeline PMID:11116089 9589839 Tmigd3 transmembrane and immunoglobulin domain containing 3 gene MP:0000229 abnormal megakaryocyte differentiation IAGP N RGD:5509061 20171005 MGI PMID:27807369 9589839 Tmigd3 transmembrane and immunoglobulin domain containing 3 gene MP:0002417 abnormal megakaryocyte morphology IAGP N RGD:5509061 20171005 MGI PMID:27807369 9589839 Tmigd3 transmembrane and immunoglobulin domain containing 3 gene MP:0005505 thrombocytosis IAGP N RGD:5509061 20171005 MGI PMID:27807369 9589839 Tmigd3 transmembrane and immunoglobulin domain containing 3 gene MP:0008254 increased megakaryocyte cell number IAGP N RGD:5509061 20171005 MGI PMID:27807369 9589839 Tmigd3 transmembrane and immunoglobulin domain containing 3 gene MP:0013704 increased megakaryocyte-erythroid progenitor cell number IAGP N RGD:5509061 20171005 MGI PMID:27807369 9589839 Tmigd3 transmembrane and immunoglobulin domain containing 3 gene MP:0013891 increased common myeloid progenitor cell number IAGP N RGD:5509061 20171005 MGI PMID:27807369 9592078 Strit1 small transmembrane regulator of ion transport 1 gene MP:0003157 impaired muscle relaxation IAGP N RGD:5509061 20160630 MGI PMID:26816378 9594329 Myhas myosin heavy chain gene antisense RNA gene MP:0000747 muscle weakness IAGP N RGD:5509061 20231116 MGI PMID:28281528 9594329 Myhas myosin heavy chain gene antisense RNA gene MP:0009402 decreased skeletal muscle fiber diameter IAGP N RGD:5509061 20231116 MGI PMID:28281528 9594329 Myhas myosin heavy chain gene antisense RNA gene MP:0009417 skeletal muscle atrophy IAGP N RGD:5509061 20231116 MGI PMID:28281528 9594329 Myhas myosin heavy chain gene antisense RNA gene MP:0009422 decreased gastrocnemius weight IAGP N RGD:5509061 20231116 MGI PMID:28281528 9594329 Myhas myosin heavy chain gene antisense RNA gene MP:0009424 decreased extensor digitorum longus weight IAGP N RGD:5509061 20231116 MGI PMID:28281528 9594329 Myhas myosin heavy chain gene antisense RNA gene MP:0009428 decreased tibialis anterior weight IAGP N RGD:5509061 20231116 MGI PMID:28281528 9632650 Gm26878 predicted gene, 26878 gene MP:0011088 neonatal lethality, incomplete penetrance IAGP N RGD:5509061 20211028 MGI PMID:28405742 9642165 Gm36723 predicted gene, 36723 gene MP:0002401 abnormal lymphopoiesis IAGP N RGD:5509061 20180426 MGI PMID:28930659 9642165 Gm36723 predicted gene, 36723 gene MP:0002411 decreased susceptibility to bacterial infection IAGP N RGD:5509061 20180426 MGI PMID:28930659 9642165 Gm36723 predicted gene, 36723 gene MP:0005016 decreased lymphocyte cell number IAGP N RGD:5509061 20180426 MGI PMID:28930659 9642165 Gm36723 predicted gene, 36723 gene MP:0005070 impaired natural killer cell mediated cytotoxicity IAGP N RGD:5509061 20180426 MGI PMID:28930659 9642165 Gm36723 predicted gene, 36723 gene MP:0008045 decreased NK cell number IAGP N RGD:5509061 20180426 MGI PMID:28930659 9642165 Gm36723 predicted gene, 36723 gene MP:0008567 decreased interferon-gamma secretion IAGP N RGD:5509061 20180426 MGI PMID:28930659 9642165 Gm36723 predicted gene, 36723 gene MP:0010766 abnormal NK cell physiology IAGP N RGD:5509061 20180426 MGI PMID:28930659 9642165 Gm36723 predicted gene, 36723 gene MP:0013667 increased immature NK cell number IAGP N RGD:5509061 20180426 MGI PMID:28930659 9642165 Gm36723 predicted gene, 36723 gene MP:0013672 decreased mature NK cell number IAGP N RGD:5509061 20180426 MGI PMID:28930659 9642623 Lhx5as1 LIM homeobox 5, antisense 1 gene MP:0001473 reduced long-term potentiation IAGP N RGD:5509061 20240321 MGI PMID:35196493 9642623 Lhx5as1 LIM homeobox 5, antisense 1 gene MP:0008428 abnormal spatial working memory IAGP N RGD:5509061 20240321 MGI PMID:35196493 9642623 Lhx5as1 LIM homeobox 5, antisense 1 gene MP:0011270 decreased excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240321 MGI PMID:35196493 9642623 Lhx5as1 LIM homeobox 5, antisense 1 gene MP:0012307 impaired spatial learning IAGP N RGD:5509061 20240321 MGI PMID:35196493 9642623 Lhx5as1 LIM homeobox 5, antisense 1 gene MP:0014372 decreased miniature excitatory postsynaptic current amplitude IAGP N RGD:5509061 20240328 MGI PMID:35196493 9651074 Ptf1aos pancreas specific transcription factor 1a, opposite strand gene MP:0000592 short tail IAGP N RGD:5509061 20141127 MGI PMID:23436999 9651074 Ptf1aos pancreas specific transcription factor 1a, opposite strand gene MP:0001258 decreased body length IAGP N RGD:5509061 20141127 MGI PMID:23436999 9651074 Ptf1aos pancreas specific transcription factor 1a, opposite strand gene MP:0002111 abnormal tail morphology IAGP N RGD:5509061 20141127 MGI PMID:23436999 9651074 Ptf1aos pancreas specific transcription factor 1a, opposite strand gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20141127 MGI PMID:23436999 9651074 Ptf1aos pancreas specific transcription factor 1a, opposite strand gene MP:0003456 absent tail IAGP N RGD:5509061 20141127 MGI PMID:23436999 9651074 Ptf1aos pancreas specific transcription factor 1a, opposite strand gene MP:0003655 absent pancreas IAGP N RGD:5509061 20141127 MGI PMID:23436999 9651074 Ptf1aos pancreas specific transcription factor 1a, opposite strand gene MP:0004704 short vertebral column IAGP N RGD:5509061 20141127 MGI PMID:23436999 9651074 Ptf1aos pancreas specific transcription factor 1a, opposite strand gene MP:0005034 abnormal anus morphology IAGP N RGD:5509061 20141127 MGI PMID:23436999 9651074 Ptf1aos pancreas specific transcription factor 1a, opposite strand gene MP:0005508 abnormal skeleton morphology IAGP N RGD:5509061 20141127 MGI PMID:23436999 9651074 Ptf1aos pancreas specific transcription factor 1a, opposite strand gene MP:0006392 abnormal nucleus pulposus morphology IAGP N RGD:5509061 20141127 MGI PMID:23436999 9658769 Bmncr bone marrow associated noncoding RNA gene MP:0004016 decreased bone mass IAGP N RGD:5509061 20191219 MGI PMID:30352426 9658769 Bmncr bone marrow associated noncoding RNA gene MP:0004989 decreased osteoblast cell number IAGP N RGD:5509061 20191219 MGI PMID:30352426 9658769 Bmncr bone marrow associated noncoding RNA gene MP:0010879 decreased trabecular bone volume IAGP N RGD:5509061 20191219 MGI PMID:30352426 9658769 Bmncr bone marrow associated noncoding RNA gene MP:0013624 decreased femur compact bone thickness IAGP N RGD:5509061 20191219 MGI PMID:30352426 9658769 Bmncr bone marrow associated noncoding RNA gene MP:0020010 decreased bone mineral density of femur IAGP N RGD:5509061 20190912 MGI PMID:30352426 9658769 Bmncr bone marrow associated noncoding RNA gene MP:0020040 decreased bone ossification IAGP N RGD:5509061 20191219 MGI PMID:30352426 9658769 Bmncr bone marrow associated noncoding RNA gene MP:0030009 increased bone marrow adipose tissue amount IAGP N RGD:5509061 20190912 MGI PMID:30352426 9667739 Cirpil cardiac ischemia reperfusion associated p53 interacting lncRNA gene MP:0031217 increased susceptibility to myocardial ischemic injury IAGP N RGD:5509061 20231005 MGI PMID:35851102 9676783 Pvrig poliovirus receptor related immunoglobulin domain containing gene MP:0000702 enlarged lymph nodes IEA N RGD:5509061 20210520 MGI 9676783 Pvrig poliovirus receptor related immunoglobulin domain containing gene MP:0001297 microphthalmia IEA N RGD:5509061 20210520 MGI 9676783 Pvrig poliovirus receptor related immunoglobulin domain containing gene MP:0002092 abnormal eye morphology IEA N RGD:5509061 20210520 MGI 9676783 Pvrig poliovirus receptor related immunoglobulin domain containing gene MP:0002339 abnormal lymph node morphology IEA N RGD:5509061 20210520 MGI 9676783 Pvrig poliovirus receptor related immunoglobulin domain containing gene MP:0002444 abnormal T cell physiology IAGP N RGD:5509061 20220707 MGI PMID:30659055 9676783 Pvrig poliovirus receptor related immunoglobulin domain containing gene MP:0004392 abnormal CD8-positive, alpha-beta T cell physiology IAGP N RGD:5509061 20220707 MGI PMID:30659055 9678351 Ttc39aos1 Ttc39a opposite strand RNA 1 gene MP:0004761 increased susceptibility to induced pancreatitis IAGP N RGD:5509061 20240516 MGI PMID:33512718 9678351 Ttc39aos1 Ttc39a opposite strand RNA 1 gene MP:0008735 increased susceptibility to endotoxin shock IAGP N RGD:5509061 20240321 MGI PMID:27315481 9678351 Ttc39aos1 Ttc39a opposite strand RNA 1 gene MP:0014433 increased cytokine level IAGP N RGD:5509061 20240516 MGI PMID:33512718 9679662 Gm34583 predicted gene, 34583 gene MP:0003043 hypoalgesia IAGP N RGD:5509061 20220922 MGI PMID:35775484 9679662 Gm34583 predicted gene, 34583 gene MP:0005166 decreased susceptibility to injury IAGP N RGD:5509061 20220922 MGI PMID:35775484 9680935 Gm15551 predicted gene 15551 gene MP:0002169 no abnormal phenotype detected IAGP N RGD:5509061 20230629 MGI PMID:35645339 9686428 Athsq3_m atherosclerosis susceptibility QTL 3 (mouse) qtl MP:0005338 atherosclerotic lesions IAGP N RGD:5509061 20150212 MGI PMID:17641228 9686428 Athsq3_m atherosclerosis susceptibility QTL 3 (mouse) qtl MP:0005385 cardiovascular system phenotype IEA N RGD:704405 20150206 MGI Created by mouse qtl pipeline PMID:17641228 9850127 Tglq6_m triglyceride QTL6 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150327 MGI Created by mouse qtl pipeline PMID:17496333 9850128 Tglq5_m triglyceride QTL 5 (mouse) qtl MP:0005376 homeostasis/metabolism phenotype IEA N RGD:704405 20150327 MGI Created by mouse qtl pipeline PMID:17496333